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ROGER D. SOiW<br />

ISSN 0541 - 4938<br />

<strong>Mycological</strong> <strong>Society</strong><br />

<strong>of</strong> <strong>America</strong><br />

NEWSLETTER<br />

Volume 41 No. 1 April 1990


SUSTAINING MEMBERS.<br />

OF THE MYCOLOGICAL SOCIETY OF AMERICA<br />

Th,e <strong>Society</strong> is very grateful for the support <strong>of</strong> its Sustaining<br />

Members. These members are lieted below; patronize them and let<br />

their representatives know <strong>of</strong> our appreciation whenever possible.<br />

AMERICAN CYANAMID CO., LEDERLE LABORATORIES, Pearl River, .New<br />

York 10965.<br />

AMYCEL, INC. (Monterey Mushrooms, Inc .) -- Producers <strong>of</strong> quality<br />

Ayaricus and exotic mushroom spawn -- 553 Mission Vineyard<br />

Road, P.O. Box 1260, San Juan Bautista, California 95045.<br />

ANALYTAB PRODUCTS, 200 Express Street, Plainview, New York 11803<br />

-- Complete line <strong>of</strong> products for the microbiology<br />

laboratory, including identification, susceptibility,<br />

instrumentation, and a new line <strong>of</strong> diagnostic virology<br />

tests.<br />

BELCCO GLASS, INC., P.O. Box B, Edrudo Road, Vineland, New Jersey<br />

08360 -- Specializing in biological glassware and<br />

equipment.<br />

BUCKMAN LABORATORIES, INC. -- Specialists in industrial<br />

microorganism control since L945 -- 1256 N. McLean Blvd.,<br />

Memphis, Tennessee 38108.<br />

CAMSCO PRODUCE COMPANY, INC. -- An affiliate <strong>of</strong> Campbell Soup<br />

Company , producer and marketer <strong>of</strong> high-quality Agaricus<br />

mushrooms, exotic m~lshrooms, and other fresh produce<br />

products -- P.O. Box 169, Blandon, Pennsylvania 19510.<br />

CAROLINA BIOLOGICAL SUPPLY COMPANY -- Serving science education<br />

since 1927 -- 2700 York Road, Burlington, North Carolina<br />

27215. (919) 584-0381, TLX 574-354 .<br />

DIFCO LABORATORIES -- The complete line <strong>of</strong> microbiological<br />

reagents and media -- P.O. Box 331058, Detroit, Michigan<br />

48232-7058.<br />

E.I. DU PONT DE NEMOURS & COMPANY, INC., Central Research and<br />

Development Department, Wilmington, DE 19880-0328<br />

FUNGI PERFECT1 -- Innovators in the demestication <strong>of</strong> wild edible<br />

fungi -- Paul Starnets, President, P.O. Box 7634, Olympia,<br />

Washington 98507. Phone (206) 426-9292; Fax (206) 426-9377<br />

GENENCOR, INC., 180 Kimball Way, S. San Francisco, CA 94080<br />

HERBARIUM SUPPLY COMPANY, INC., P.O. Box 883003, San Francisco,<br />

California 94188. (415) 584-7000.<br />

HOECHST-ROUSSEL PHARMACEUTICALS, INC., Dr. Beatrice B. Abrams,<br />

Route 202-206, Sommerville, New Jersey 08876.<br />

HOFFMANN-LAROCHE, INC., Research Division, Nutley, New Jersey<br />

07110. (201) 235-5000; N.Y .C. (212) 695-1400.<br />

JANSSEN PHARMACEUTICA -- World leader in antimycotic research --<br />

40 Kingsbridge Road, Piscataway, New Jersey 08854.<br />

THE R. W. JOHNSON PHARMACEUTICAL RESEARCH INSTITUTE -- A Research<br />

and Development Management group for JOHNSON & JOHNSON<br />

pharmaceutical companies -- LaJolla, California; Raritan,<br />

New Jersey; Spring House, Pennsylvania; Toronto, Canada;<br />

Zurich, Switzerland.


<strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> <strong>America</strong><br />

NEWSLETTER<br />

Volume 41, No. 1; April, 1990<br />

Terrence M. Hammill, Editor<br />

Department <strong>of</strong> Biology<br />

SUNY College at Oswego<br />

Oswego, New York 13126<br />

(315) 341-2768 (Laboratory)<br />

(315) 341-3031 (Department Off ice)<br />

(315) 342-3074 (Home Answering Machine)<br />

TABLE OF CONTENTS<br />

Sustaining Members ---------------------<br />

Table <strong>of</strong> Contents ......................<br />

Editor's Comments ----------------------<br />

Abstracts <strong>of</strong> Papers and Posters --------<br />

Additional Authors <strong>of</strong> Abstracts --------<br />

Changes <strong>of</strong> Address and/or Phone Number -<br />

Forthcoming Events ---------------------<br />

<strong>Mycological</strong> Services Available ---------<br />

Fungi Wanted ---------------------------<br />

Publications and Computer Programs<br />

for Give-Away, Sale, or Exchange -----<br />

New Books by Members -------------------<br />

Publications Needed --------------------<br />

Vacancies for Mycologists --------------<br />

Assistantships and Fellowships ---------<br />

Employment Desired ---------------------<br />

Major Honors, Awards, and Promotions ---<br />

Changes in Affiliation or Status -------<br />

Notes and Comments ---------------------<br />

COVER ILLUSTRATION: Wucor ntucedo. Mature sporangium.<br />

Magnification bar = 20 micrometers; X 900. Micrograph by T.M.H.


Editor's Comments<br />

April, 1990<br />

First announce-: David J. McLaughlin, Department <strong>of</strong><br />

Botany, University <strong>of</strong> Minnesota, St. Paul, MN 55108, is the new<br />

Editor-in-Chief <strong>of</strong> Mvcolouia, succeeding Ron Petersen ; Kudos<br />

clearly are in order for the outstanding job done by Ron Petersen<br />

and his staff at the University <strong>of</strong> Tennessee. Good luck, Dave!<br />

Thanks for the kind comments from several <strong>of</strong> the MSA members<br />

who sent them to me after the October, 1989, issue came out.<br />

With this second issue prepared here at SUNY-Oswego, I wish to<br />

acknowledge the assistance <strong>of</strong> three undergraduate students who<br />

provided much logistical help for both issues, seniors --<br />

Jennifer Collart and Monica Converse (paid with Newsletter<br />

support funds) -- and the frosh, Melissa Matolchi (a work-study<br />

student assigned to my laboratory). Those three spent many hours<br />

labelling, stuffing, sorting, bagging, handling, and doing other<br />

kinds <strong>of</strong> dog-body labor, and I could not have done without their<br />

help! I also want to thank June Johnston, Director <strong>of</strong><br />

SUNY-Oswego Publications, and her assistant, Jody Longeill, for<br />

their valuable advice and quality work. The Newsletter was<br />

something <strong>of</strong> a new challenge for them and their staff, and I<br />

think the results have been excelleht.<br />

There are a couple <strong>of</strong> minor changes in the blue Newsletter<br />

Questionnaire (corrected typographical errors, a rearrangement <strong>of</strong><br />

some items, and a new item -- New research projects). I think I<br />

have it about right, but suggestions for change are welcomed.<br />

There are three inserts:<br />

A. The M A Newsletter Questionnaire (blue)<br />

B. The Ernployee/Employer Data Form (green -- new address for Bob<br />

Pohlad)<br />

C. An MSA Newsletter Survey (yellow)<br />

I arranged the Abstracts <strong>of</strong> Papers and Posters presented at the<br />

Annual Meeting <strong>of</strong> MSA immediately following these comments. The<br />

Abstracts are listed alphabetically by the first author;<br />

additional authors are listed alphabetically following the<br />

listing <strong>of</strong> Abstracts (pages 46-48). The remaining pages (49-68)<br />

are from the MSA Newsletter Questionnaires returned since the<br />

October issue, 1989. Since I typed those pages where typing was<br />

needed, any errors are my fault, and I apologize in advance.<br />

It has been a pleasure preparing the past two issues.<br />

However, since I am not sure whether those two issues have been<br />

able to meet the needs <strong>of</strong> the membership, I have included a<br />

survey as an aid to preparation <strong>of</strong> future issues. Please<br />

respond. I want'to make the Newsletter as good as it can be<br />

(within my limitations), and you can help. Also, if you have<br />

suitable items (artwork, anecdotes, etc.) which can function as<br />

page fillers when there is a need, please forward them to me.<br />

Best wishes; I hope to see you at the meeting in Madison.<br />

Sincerely,<br />

7&mLL.e<br />

Terrence M. Hammill, Editor<br />

MSA Newsletter


Abstracts <strong>of</strong> Papers and Posters<br />

S. K. ABOULLiJl, A'L.!~.XL-SAUJCX 8. A-ISSh<br />

Liology depertment, Collep? <strong>of</strong> Science,<br />

University <strong>of</strong> dasi*uh, 3asrd1, IMQ.<br />

iff e ct <strong>of</strong> ternpereture, relztive humieity and<br />

inf loreccence extract on the mycelial growth<br />

m Z conieicl geminetion cf I..euf:inelle<br />

--- !iccett&e Ctrv., tile caus~l p~:ti.,oel: <strong>of</strong><br />

infloreecene rot Cisease <strong>of</strong> date palm.<br />

The infiorescence rot disease caused by<br />

Laufiinella scaettae iu the most important<br />

diseese three tin^ cbout 30 nfllions date<br />

pclm trees in Iraq. The temperature range<br />

for .the mycelial growth, conidial germimtion<br />

and conidial germ tube length was between<br />

10 and 3C C. The optimum temperature for<br />

the mycelial growth, geninetion <strong>of</strong> conitia<br />

auG gem tube length was occurred at 20 C.<br />

Best mycelial growth and conidial production<br />

occu~red at r.h , vrhile best conidial<br />

germination occurred at 95% r.h. Tissue<br />

extract obt~ined from inflorescence <strong>of</strong><br />

i'bidraai, Zahdl and Khikri cultivars<br />

enhances conidial germination xhile extract<br />

obtainee from inf lorescene <strong>of</strong> 1;hcnmi<br />

cultiver snowed inhibitoq effect.<br />

M.F.ALI FN. C.F. FRIESE. E.B. ALLEN, and LM. SHULTZ, Dept <strong>of</strong><br />

Biology, Systems Ecology Research Group, San Diego State<br />

University. San Diego, CA 92182-0057 and Dept <strong>of</strong> Biology,<br />

Utah State University, Logan UT 84322-5305.<br />

VA rnycorrhizal fungi associated with<br />

tridentata across Western North <strong>America</strong>.<br />

VA mycorrhizal fungi associated with a single subspecies <strong>of</strong> plant.<br />

Basin Big Sagebrush, were collected over the entire range <strong>of</strong> its<br />

distribution during the growin6 season <strong>of</strong> 1989. Sites sampled<br />

range@ from Baja California. Mexico to British Columbia, Canada,<br />

to North Dakota, to New Mexico. Ten 3 cmxl0 cm deep cores from<br />

different shrubs were taken at each site and analyzed for VAM<br />

fungal species composition and density, % root infection, soil<br />

water and soil P. G)omus was common among most sites.<br />

The fungi were predominantly GI. trom the Baja<br />

Peninsula and across the desert through California and New<br />

Mexico. Sjlomus tonuosum was common in Nevada and Baja<br />

California. GI. predominated in the central Great<br />

Basin. GI, was common from British Columbia to<br />

North Dakota. Glaaswra was common in North Dakota.<br />

Scutelloswra extended from southwestern Wyoming<br />

across to Reno Nevada. -. were common across New<br />

Mexico. Nevada, and California. There is a wide diversity <strong>of</strong> VAM<br />

fungi associated with a single wide ranging plant subspecies.<br />

Thus, the species composition <strong>of</strong> fungi appear to be regulated in<br />

part by habitat.<br />

- Z. -Q. AN, J. W. HENDRIX, D. E. HERSXMAN,<br />

and G. T. HENSON. Department <strong>of</strong> Plant .<br />

Pathology, University <strong>of</strong> Kentucky, Lexington<br />

40546.<br />

Endogonaceous mycorrhizal community<br />

associated with soybean as affected by crop<br />

rotation and soil fumigation.<br />

Propagules <strong>of</strong> mycorrhizal fungi in a Western<br />

Kentucky field highly productive for soybean<br />

and previously planted for two years to<br />

corn, milo, fescue, or soybean were<br />

determined by HPN bioassay before and after<br />

fumigation with 67% methyl bromide-33%<br />

chloropicrin and throughout a season in the<br />

production <strong>of</strong> a crop <strong>of</strong> soybeans. Twenty<br />

species <strong>of</strong> Endogonaceae, mostly Glomus<br />

species, were found. In soybean plots, soil<br />

fumigation eliminated most propagules in the<br />

upper 15 cm <strong>of</strong> soil; but after production <strong>of</strong><br />

a crop <strong>of</strong> scybeans, populations <strong>of</strong> total<br />

propaqules recovered to prefumiqation<br />

numbers and were higher than populations in<br />

non-fumigated soil. Soil from plots grown<br />

continuously to soybean had fewer species<br />

and lower populations <strong>of</strong> propagules <strong>of</strong><br />

Glomus spp. than plots rotated with the<br />

other three crops; however, populations <strong>of</strong><br />

Giuas~ora spp. were high in continuous<br />

soybean plots. Populations and number <strong>of</strong><br />

species were higher in fescue plots than in<br />

the others. Colonization <strong>of</strong> roots did not<br />

become extensive until about eight weeks<br />

after planting, about the time plants<br />

entered the reproductive phases.<br />

D. A. ANDERS and J. C. ZAK Ecology Research Group,<br />

Dept. <strong>of</strong> Biological Sciences, Texas Tech University,<br />

Lubbock. -. TX 79409.<br />

~ ~~~ ~<br />

species abundance and seasonality <strong>of</strong> wood-decomposing<br />

basidiomvcetes from woodrat middens in the Chihuahuan and<br />

Sonoran beserts.<br />

Woodrat middens may function as important centers <strong>of</strong> wood<br />

decomposition in desert ecosystems. This smdy examined the<br />

spatial and temporal occurrances <strong>of</strong> wood decomposing<br />

basidomycetes on wood from middens in the Chihuahuan and<br />

Sonoran deserts. Distinct temporal and spatial variability in<br />

numbers <strong>of</strong> species and species composition were observed.<br />

The majority <strong>of</strong> basidiomycetes from both deserts were<br />

isolated during Aupst. A greater number <strong>of</strong> species were<br />

isolated from middens in the Sonoran verses the Chihuahuan<br />

desert at all sampling times. Although the two deserts shared<br />

species in common, the fungal species composition <strong>of</strong><br />

middens in the Sonoran did differ from the Chihuahuan.<br />

Penio~hora ramaricicola was predominately found in the<br />

Chihuahuan rather than the Sonoran. Differences in the<br />

species composition <strong>of</strong> the basiaiomycete assemblages<br />

assiciatea with woodrat middens could result in differing<br />

wood decomposition rates between the two desen ecosystems,<br />

and the importance <strong>of</strong> middens to the overall decomposition <strong>of</strong><br />

wood.


- ROGER %. -<br />

ANDERSON and A. E. LIBERTA. Biology Dept.<br />

1llinoi.s State University, Normal, IL 61761.<br />

VAM colonization and growth <strong>of</strong> little bluestem grass<br />

(Schizachyrium scoparium) in fumigated and nonfumigated<br />

soil.<br />

Little bluestem grass was grown in fumigated and<br />

non-fumigated sandy, low nutrient soil to which<br />

was added supplemental N, P. K and Ca and Mg (bases).<br />

In non-fumigated soil, between the first and second<br />

growing seasons plants decreased in mean percent<br />

colonization (36.9 vs. 20.8%) and colonized root<br />

length (2,438 vs. 1,627 cm), except for the base<br />

treated plants that increased in colonized root<br />

length between the first and second growing season<br />

(2,625 vs. 3,473 cm). In contrast, in fumigated<br />

soil plants increased in mean percent colonization<br />

(1.3 vs. 3.2%) and colonized root length (100 vs.<br />

445 cm) between the first and second growing seasons.<br />

In the second growing season, base treated plants<br />

produced the most biomass per plant in fumigated<br />

and non-fumigated soils. The soils are relatively<br />

high in available P (14-28 ug/g) but low in<br />

available Ca (276-482 ug/g) and Mg (59-76 uglg).<br />

The results indicate that mycorrhizae may enhance<br />

plant growth in our soil when limiting nutrients<br />

(Ca and Mg) are provided.<br />

R.K. ANTIBUS, DEBRA B. SINSABAUGH AND A.E.<br />

LINKINS 111. Biology Department, Clarkson<br />

University, Potsdam, NY 13699. The effects<br />

<strong>of</strong> phosphorus source on acid phosphatase<br />

activity and phosphorus uptake in<br />

ectomycorrhizal fungi.<br />

Six ectomycorrhizal fungi were grown witk<br />

low leveis <strong>of</strong> inorganic or organic<br />

phosphorus (phytic acid) to determine tht<br />

effects <strong>of</strong> P source on isozyme patterns,<br />

acid phosphatase activity and uptake <strong>of</strong> 3 2 ~<br />

inositol phosphate. Isolates studied<br />

inc1uded:~~enococcum eo hilum, Scleroderma<br />

cltrinum, Hebelomz cr%dki?orme,<br />

Lactarius sp., Amanita rubescens and<br />

Entoloma sericeurr,. Significant<br />

interspecies difterences were observed in<br />

isozyme patterns and cell surface acid<br />

phosphatase activity. Phosphorus source,<br />

either inorganic or organic P, did not<br />

affect isozyme patterns and generally did<br />

not influence phosphatase production.<br />

However, C. eo hilum demonstrated a five-<br />

fold i n c r e a s h<br />

surf ace phosphatase<br />

activity when grown on organic P. In<br />

general 32 P uptake from inositol phosphate<br />

correlated well with cell surface<br />

phosphatase activity. Growth on phytic<br />

acid increased uptake <strong>of</strong> 32~, with this<br />

+<br />

effect being most pronounced in C.<br />

aeo hilum. These results provide evidence<br />

or the involvement <strong>of</strong> phosphatase in<br />

organic P utilization.<br />

R.K. ANTIBUS, TIMOTHY P. WEILAND, AND R.L.<br />

SINSABAUGH. Biology Department, Clarkson<br />

University, Potsdam, NY 13699. Growth and<br />

production <strong>of</strong> hydrolytic enzymes by<br />

Phellinus igniarius and Piptoporus<br />

betulinus in pure cultures and on birch<br />

wood.<br />

Phellinus igniarius and Pi to orus<br />

betulinus are common macro +?!7<br />

ungi o standing<br />

dead birches in upstate New York. Our study<br />

objectives were to compare hydrolytic<br />

enzymes for these fungi whem grown in pure<br />

culture, and to determine whether similar<br />

patterns <strong>of</strong> growth and enzyme production<br />

were observed on birch wood in microcosms<br />

containing different soil types. when<br />

grown with cellobiose as a carbon source P.<br />

betulinus showed higher total activities<br />

t an P. i niarius <strong>of</strong> #-glucosidase,<br />

e 2 d o c e l l h xylosidase. Both fungi<br />

produced similar levels <strong>of</strong> exocellulase in<br />

culture, and P. i niarius produced higher<br />

acid phosphatase zctivities. These<br />

patterns <strong>of</strong> enzyme production remained<br />

consistent when fungi were grown on birch<br />

sticks in microcosms. Birch stick mass loss<br />

was affected by fungus and soil type used<br />

in microcosms. P. i niarius generally<br />

caused higher m ~ s s b p. n betulinus.<br />

When the two fungi were combined on single<br />

resource units mass loss was less than for<br />

individual species grown separately.<br />

Differences in mass loss paralleled<br />

biomass accumulation, measured by ATP and<br />

ergosterol, in resource units.<br />

PARTHA BANEWE. Dept. <strong>of</strong> Biology, Illinois State<br />

University, Normal, IL 61761 (Presently at the Dept. <strong>of</strong> Plant<br />

Biology. Southern Illinois University, Carbondale, 1L 62901).<br />

Laboratory experiments on competition between two<br />

rhizoplane fungi Penicillium chrvso- and Trichoderma<br />

hardanurn.<br />

Based on results <strong>of</strong> a field study involving rhizoplane<br />

micr<strong>of</strong>ungi associated with little bluestem (Schizachyium<br />

scovarium], a common tallgrass prairie species, it was<br />

hypothesized that Penicillium ~~IVSOE- and Trichoderma<br />

harzianum outcompeted each other in unfumipted and<br />

fumigated soils, respectively. To test this hypothesis and<br />

investigate the mechanisms <strong>of</strong> competition, interactions<br />

between the two fungi were stuhed in laboratory experiments<br />

using an artificial model system. Competition did occur.<br />

Instances <strong>of</strong> advantageous priority effects caused by one<br />

organism on the other were also established. In addition,<br />

some demmental residual effects on the growth <strong>of</strong> one species<br />

were observed when it was grown along with the killed mass<br />

<strong>of</strong> the other in the same numtive h u m employed prior w<br />

killing.<br />

Mark T. Banlk. Michael J. Larsen. Harold H. Burdsall. Jr. Center<br />

for Porest Mycolory Research. Porest Products Laboratory.<br />

USDA-Pores1 Service. Madison. W1. Thc formation <strong>of</strong> clamp<br />

connections between compatible baaidiospore germlinr8 <strong>of</strong> species<br />

<strong>of</strong> Armillaria.<br />

Basidioapore dilutions on rater agar <strong>of</strong> meveral North A ~~SIC.~<br />

biological species (NABS) <strong>of</strong> Armillaris were examined for the<br />

presence <strong>of</strong> clamp connections followinp germination and formation<br />

Of "juvenile hyphae'. After two wceks all spore dilutions<br />

examined exhibited clamp connections. These included six


isolates each Of NABS 1 and 111. two <strong>of</strong> NABS V and 11 <strong>of</strong> NABS<br />

VII. Ccrmlnmled sport. from tnc same fruitin# body for two<br />

isolates <strong>of</strong> NABS I and two iaolates <strong>of</strong> NABS VII were palred on<br />

water agar. Clamps were observed in 23-36 percent <strong>of</strong> theme<br />

Dairingr. a value that is son.i.ten1 with Inr expected number for<br />

a bifactorial mating system. Intrampeelem pairings <strong>of</strong> serminated<br />

bamidlompores <strong>of</strong> two imolates <strong>of</strong> NABS 1 mnd two isolates <strong>of</strong> NABS<br />

Vl1 were lOOX coapatibllc. ba-cd on clamp formation Indleatlng<br />

bultiallellsm at the incompatibility loci. Intermpecific<br />

palrinss Of apores from one imolate each <strong>of</strong> NABS 1 and V11 laeked<br />

Clamp connections. Agar plug. from the vmrioul p.irInsm were<br />

transferred to an enriched medium in order to observe colony<br />

morphology. Transfers from spore pairlnls involvlns NABS VI1<br />

were <strong>of</strong>ten uninterpretable. Translerm from NABS I spore pairins.<br />

exhibited the expected "fluffy" or "crusto8e" colony morphology<br />

accordlne to the absence or presence <strong>of</strong> clamp connections.<br />

Confrontations <strong>of</strong> haploid isolates ("non-Juvenile" hyphse) from<br />

the same fruitins bodies that ylelded the mporce for pairing.<br />

provided date comparsble to those obtained through the use <strong>of</strong><br />

Clamp formation. Clamp connection iormatlon between "Iuvenile<br />

hyphae" <strong>of</strong> compatible basidiosporem may <strong>of</strong>fer an additional tool<br />

for the deflnltion <strong>of</strong> specie. in Armillaria.<br />

TIKmy J. BARM, sl!Jzvm J. tKmciLm1 d SWlT A.<br />

Q3RD&. l~eparbnent <strong>of</strong> Biological Sciences, State<br />

University <strong>of</strong> New York, College at Cortland, Cortland,<br />

NY 13045 ard l~eparbnent <strong>of</strong> Batany, Vnive~<br />

sity <strong>of</strong> lbmese, Knoxville, ?N 37916<br />

pvcena leaiam (Perk.) Saho: culture mat characteristics,<br />

mating studies and analysis <strong>of</strong> in vitro<br />

basidiome prcduction.<br />

?he production <strong>of</strong> agaric basidimata in pxe culture<br />

is the exa?ption and oertainly a too infrequent<br />

phenomenon. Many different species <strong>of</strong> rmshrogm can<br />

be enticed to prpduce myoelial mats in culture, howwer<br />

the vast majority <strong>of</strong> these captxred individuals<br />

rarely will undqo a caplet& life cycle frcun basidiospore<br />

to basidiospore in the laboratory. A re cent collection and isolaticm <strong>of</strong> an individual <strong>of</strong><br />

Wce~ leaiam (#3 SAG/#6113 TJB), fran a decayirq<br />

beech log in oentrdl New York, has been &eerfully<br />

prcrcfucing its exquisitely colored caespitose clusters<br />

<strong>of</strong> basidicmta on MEA and other media in plre culture<br />

in the laboratory. Phenatypic plasticity <strong>of</strong> the<br />

monokaryatic and dikryotic mycelial mats will be<br />

shwn and discussed. The mating system for this in-<br />

&vidual is tetrapolar. Mon&&yotic basidimata<br />

production is <strong>of</strong>ten initiated but becgnes arrested at<br />

&f ferent plases <strong>of</strong> stipe elongation and pileus formation.<br />

A mpmductive hymenium is never formed in<br />

the monokaryotic basidicpne producers. w e in all<br />

parts <strong>of</strong> the basidiaane are generally dikaryotic, the<br />

spores are mkaryotic. An analysis <strong>of</strong> the macroand<br />

mirroscopic characters <strong>of</strong> this species as it occurs<br />

in culture will be presented and mapared to<br />

those diagnostic features that are used to recognize<br />

this agaric in its MW habitat.<br />

P. BAYMAN and P. J. COTTY. USDA Southern<br />

Regional Research Center, P.O. Box 19687,<br />

New Orleans, LA 70179.<br />

Aflatoxin production and genetic variation<br />

in A s D ~ ~ u flavus. ~ ~ ~ u s<br />

Aspernillus flavus is notorious for<br />

variability in aflatoxin production, both<br />

between and within strains. Because A.<br />

flavus is asexual, population genetics <strong>of</strong><br />

aflatoxin production has been difficult<br />

to study. We determined genetic<br />

relatedness among isolates <strong>of</strong> A. flavus<br />

using vegetative compati bi 1 it; tests.<br />

Variation in aflatoxin production<br />

vitro was significantly greater among<br />

vegetative compatibility groups (VCGs)<br />

than among members <strong>of</strong> single VCGs.<br />

Several quantitative aspects <strong>of</strong> aflatoxin<br />

production was significantly consistent<br />

within VCGs. Implications for stability<br />

and inheritance <strong>of</strong> aflatoxin production<br />

will be discussed.<br />

ABBES BELKHIRI, JOHN BUCHKO and GLEN R. KLASSEK<br />

Dept. <strong>of</strong> Microbiology, University <strong>of</strong> Manitoba,<br />

Winnipeg, Manitoba, Canada, R3T 2N2.<br />

Species assignment <strong>of</strong> Pythium isolates by PCR amplification<br />

and restricti~ibosomal DNA.<br />

A method for rapid assignment <strong>of</strong> Pythium isolates to<br />

species was developed based on a neuiprep for<br />

DNA isolation and on poiymerase chain reaction (PCR)<br />

amplification <strong>of</strong> several sections <strong>of</strong> the rDNA repeat,<br />

including the intergenic region. PCR products were<br />

digested with batteries <strong>of</strong> restriction enzymes and<br />

the resulting RFLPs were used to determine species<br />

clustering. Consensus patterns for 15 species <strong>of</strong><br />

Pythium were determined. In several cases the method<br />

was useful in resolving taxonomic problems insoluble<br />

by morphological criteria, and in classifying isol-<br />

lates which do not produce oogonia or zoospores and<br />

thus are difficult to classify. PCR results were com-<br />

pared with RFLP pr<strong>of</strong>iles <strong>of</strong> mitochondria1 DNA to<br />

confirm the reliability and internal consistency <strong>of</strong><br />

the molecular approach. The PCR approach is more<br />

rapid and convenient than the use <strong>of</strong> labelled probes<br />

and it provides enough information for species assip-<br />

nment so that full sequencing <strong>of</strong> DNA segments from<br />

each isolate is not necessary.<br />

J. W. ECRETT. Department <strong>of</strong> Biology, Tulane Uni ver-<br />

sity, New Orleans, LA 70118. Nitrogen control <strong>of</strong><br />

secondary metabolism.<br />

Secondary metabolites are low molecular weight com-<br />

pounds <strong>of</strong> diverse chemical structure, that occur in<br />

families <strong>of</strong> related metabolites, have erratic taxon-<br />

omic distribution, are usually synthesized after ac-<br />

tive growth has ceased, and serve no obvious function<br />

in cellular metabolism. The best known fungal metab-<br />

olites are bioactive compounds such as antibiotics,<br />

mycotoxins, and immunosuppressants. Secondary.metab-<br />

olite production is sensitive to nutritional control.<br />

Fermentation microbiologists have developed a large<br />

data base about the role <strong>of</strong> nitrogen in maximizing<br />

industrial production <strong>of</strong> economically important com-<br />

pounds. A temporal relationship between the deple-<br />

tion <strong>of</strong> nitrogen and the initiation <strong>of</strong> polyketide<br />

mycotoxin synthesis is common1 y observed in submerged<br />

culture. Ammonia and complex amino acids are pre-<br />

ferred nitrogen sources for aflatoxin and anthraqui-<br />

none biosynthesi s. Despite the enormous phenomenol-<br />

ogical literature, no generalized mechanism for<br />

nitrogen control <strong>of</strong> fungal secondary metabol ism has<br />

been elucidated.


p. BERRa, G. SAENZ, T. WHITE and J. TAYLOR,<br />

Department <strong>of</strong> Plant Biology, University <strong>of</strong><br />

California, Berkeley, CA 94720 and H<strong>of</strong>fmann-<br />

La Roche, Emeryville, CA 94608.<br />

Molecular resolution <strong>of</strong> conflicting<br />

cleistothecial and condial characters in<br />

Talaromvces and relatives?<br />

We are interested in whether the sexual<br />

characters defining the genus Talaromvces or<br />

the asexual characters <strong>of</strong> species within<br />

Blaromvces are better predictors <strong>of</strong><br />

phylogenetic relationships. T m<br />

delimited from other Trichocomaceae by sexual<br />

characters, i-e., s<strong>of</strong>t cleistothecia with<br />

walls <strong>of</strong> loosely interwoven hyphae. Most<br />

Talaromvces species have penicillium<br />

,anamorphs but a few (e.g., 2. Jevcettanus or<br />

T. bvssochalmvdoides) produce Paecilomvces<br />

asexual states. These paecilomvces states<br />

resemble the anamorphs <strong>of</strong> ~vssochlamvs and<br />

Thermoascus species. Dlaromvces species may<br />

be monophyletic, as implied by current<br />

taxonomy, or they may be polyphyletic with<br />

the Paecilomvces-producing species being more<br />

closely related to pvssochlamvs and<br />

Thermoascus than to the Penicillium-producing<br />

Talaromvces species. To test these<br />

hypotheses we have developed a character set<br />

for these taxa independent <strong>of</strong> cleistothecial<br />

and conidial characters. Phylogenies<br />

inferred from DNA sequence <strong>of</strong> the internal<br />

transcribed spacer <strong>of</strong> the ribosomal DNA<br />

repeat unit and the 5.8s rDNA will be<br />

compared to phylogenies based on<br />

cleistothecial and condial characters to<br />

evaluate the phylogenetic value <strong>of</strong> these<br />

characters.<br />

Jzmes D. Bever, Department <strong>of</strong> Botany, Duke<br />

University, Durham, NC, 27706.<br />

Differentiation <strong>of</strong> Natural Allium vineale<br />

Populations in Response to Mineral Versus<br />

Biotic Components <strong>of</strong> Soil.<br />

Allium vineale bulbils from 10 individuals<br />

from each <strong>of</strong> three populations were grown<br />

in pots <strong>of</strong> pasteurized soil inoculated with<br />

fresh or autoclaved whole soil inoculum<br />

from each site <strong>of</strong> these three populations.<br />

Plants grew larger with fresh soil inocu-<br />

lum. This effect is likely to be due to<br />

mycorrhizal fungi. The total plant weights<br />

were greater when grown with their own<br />

inoculum than when grown with other inocu-<br />

lum -- regardless <strong>of</strong> whether the inoculum<br />

was fresh or autoclaved. This suggests<br />

that the Allium populations are adapted to<br />

the mineral component <strong>of</strong> their native<br />

soils. Bulb weights were also greater when<br />

grown with their native soils. However,<br />

the populations grew relatively better with<br />

their own soii amongst the autoclaved<br />

inoculum than with their own soil amongst<br />

the fresh inoculum. This result suggests<br />

that these populations are locally adapted<br />

to the mineral -- but not the biotic compo-<br />

nent <strong>of</strong> the soil.<br />

is<br />

Q, BER-. M. E. BORAAS, and K. H. NEALSOK.<br />

University <strong>of</strong> Wisconsin-Milwaukee. Center for Great<br />

Lakes Studies, 600 E. Greenfield Avenue,<br />

Milwaukee. WI 53204.<br />

In vitro antagonism <strong>of</strong> bioluminescent fungi by<br />

Trichoderma harzianum.<br />

Two species <strong>of</strong> bioluminescent fungi. Panellus stypticus<br />

and Omphalotus olearius were placed in contact with three<br />

different strains <strong>of</strong> Trichoderma harzianum.. Subsequent<br />

light emission by the luminous fungi and advance <strong>of</strong> [he<br />

fungal pathogens were compared. Relativc diffcrcnces<br />

among the pathogens were reflected in the rate <strong>of</strong><br />

mycelial advance, the total area over khich spores were<br />

produced upon l e host fungi. and decreases in host<br />

bioluminescence. After ten days differences in the total<br />

surface areas <strong>of</strong> spore production varied from 1 to 53<br />

percent. Differences in the reduction <strong>of</strong> bioluminescence<br />

<strong>of</strong> the same material ranged over 2 orders <strong>of</strong> magnitude.<br />

Final reduction in luminescence ranged over 6 orders <strong>of</strong><br />

magnitude. Marked reduction in bioluminescence was<br />

observed to precede the advance <strong>of</strong> spore production. The<br />

greatest reduction in luminescence was correlated with<br />

the presence <strong>of</strong> T. harzianum hyphae. Two strains <strong>of</strong><br />

T. harzianum, NRRL 1698 and ATCC 58674, were capable <strong>of</strong><br />

killing both bioluminescent fungi within the study period<br />

while a third strain, NRRL 13019, was capable <strong>of</strong> killing<br />

only Omphalorus olearius.<br />

L. B'iTlKCI & S. LLPO. Ccntml gmdh <strong>of</strong> Scleratim cepivonm by<br />

several strains <strong>of</strong> Trichodem sw.<br />

Antagonistic activity <strong>of</strong> 60 strains <strong>of</strong> Trict-dem spp. (T. harzianun,<br />

T. hmtvn, T. kmirgii, T. s a t u n i i Sclemtiunii<br />

vfi ~ a n a ~ s d 7 l&ratory Z E ccndiiuns.Tne pam<br />

i q e was ~lployed to detect the activity <strong>of</strong> the diffusible<br />

mtablites on mycelial grwth anc: sclemtia fomtion. Sun?<br />

strains <strong>of</strong> all species except T. satmnism produced 1Wb qwth<br />

inhibition at 24 h. A reduced3 <strong>of</strong> strains <strong>of</strong> all species were<br />

able to inhibit sclemtial formation, at 12 d, Wen sclerotia<br />

mtvration was cnpletly achieved in the ccrcml disks. Ftycelial<br />

cords, larger sclerotia (3-5tim the cahm! size) and little;<br />

stalked, imture ones (formirg the rind later) were fonred by<br />

other set <strong>of</strong> strains with lwr activity. ha1 cultures on agarmlt,<br />

using cne sclerotiun and a mycelial disc <strong>of</strong> Trichodem as<br />

iimla, were carried art. The cutmna cbserwd with the mst<br />

;active strains were: 1) yellw pignntatim in the interface zone<br />

and - S. cepivonm grwing just to the <strong>of</strong> Trichodem advancing<br />

zcne, where MTI? new sclerotia fomtion ocarrred; 2j sclemtia<br />

germination inhibited; 3) sclerotia germination produci~ xne new<br />

sclemtia; Trichoderma, in turn, inhibited Wse I?& sclerotia<br />

germination and covered them by a heavy sprulatim. In cases 2 and<br />

3 MTI? sclemtia were apty and others internally disorganized,<br />

spliting under a little pression. In Loth situatims sclerotia or<br />

fragnwrts <strong>of</strong> them were mble to gwminate Wm transfered to fresh<br />

Mia or <strong>of</strong> they did new sclerotia were not f d . Mycoparasitirm<br />

<strong>of</strong> myceliun or sclemtia were not cbserwd. Experimsrts under field<br />

conditions, with several strains <strong>of</strong> Trichodem will be perfo&,<br />

ladting for a possible biolcgical mml <strong>of</strong> mion witkrrst'idisease.


J. li BHAlTACHAWJEE. Department <strong>of</strong> Micrubidogv<br />

Miami University, Oxford. OH 45056<br />

!The Unique Biosynthet~c Pathway for Lysine in Fungi<br />

ibim Is an essential amino acid (obtained from diet) for humans and animals.<br />

:Havcr, it is synthesized by ruo mutually exclusive pstbways in bneterio, lunpi,<br />

iand plants. Bscterin, piants, and certain pbycomywtes usc the diaminop~wlic acid<br />

pathm my, wbe~lls the yeastsandother hther fuqi use Ibea-sminosdipte pathway<br />

ifor the biosvnthesis <strong>of</strong> Ivrine. Genetic and biochemical analysis <strong>of</strong> lvsine<br />

taurotmphs <strong>of</strong> SacchammvcPs mmisiar have confirmed eight en- steps and<br />

lmore thmn mlve unl~nked pews responsible for the a-smimdipate pathway.<br />

iHomocitrate spthase cntaI.yzes the firs1 committed step (a-kctoglumnte + acevl<br />

CaA - homncitnte) <strong>of</strong> the pathway. Homocitrate - cis-homoaeonitate -<br />

.homoisocitrntr - a-ketoadipate - a-sminoadipate are the intermediates <strong>of</strong> the first<br />

:half <strong>of</strong> the patbuay luclll~ud inside mitochondria and the specific ~ctiuns are<br />

.analopus to tho= ol the cllric acld cycle lead~tq to the synthesis <strong>of</strong> glutamate.<br />

la-Aminondipate - a-sminondipte-scmialdchyde - saccharopine - lysine constitute<br />

!the second half <strong>of</strong> the pathway. Homocltrate sytbase. homoimitrate<br />

~dehydrugenase. a-sminoadipate roduetase, saccbampine debywnase hnve been<br />

!purified sod characterized from wild type S. previsiae. ?be cis-homuumnitase and<br />

!a-kctondipate transsminase have been parIiall!. characterized. The presence <strong>of</strong> one<br />

tor more <strong>of</strong> these enzymes has also heen demonstrated in scveral psts and molds<br />

! i n c l u d i n g Y a r m w i a ~ Neu--,and ~ ~ ,<br />

&nicillium<br />

pbrvsonenum. Homoc~trate synlhase is leedhuck inhibited by lysine and its<br />

~analogues, all <strong>of</strong> the enryws erhibit repression when S. fcmvisiae is pmm in<br />

llvs~ne supplemented medium. and the enzymes <strong>of</strong> tbe -d ball d tbe pathway<br />

~are under the pcneral rqyhtion <strong>of</strong> amino acids syathcslk Several lysioc penes<br />

lhave been cloned bv functional complementation <strong>of</strong> specific lysine auxotrophs with<br />

!plasmids fmm a S. gerevisiae pnomic library. The cloned pcne in the<br />

ipiasmid YEp620 Is localized on a 6.9 kb Pstl-EeoRI DNA inserl, tbe pene is<br />

clocsl~zed on a 2.8 kb Xhol-Xhol DNA inserl <strong>of</strong> the plasmid pS052. t h e m pene<br />

is localized on a 3.2 kb Sphl-BamHI DNA insert <strong>of</strong> the pSCS plasmid, and the<br />

'm pene is localized on a 1.9 kh BamHI-Xbal DNA insen <strong>of</strong> the pS051 plasmid<br />

Lvsine is an important fermentation product. Also, the a-aminondipale pathway<br />

wn be used as a marker lor phvlupeny as we11 as a tawt lor tbe rapid detection<br />

and wntml <strong>of</strong> important oppnnunistic funel patbopcns. Lysine is not cataholizod<br />

as sole nitmgen wum h?. S. rrrevisiae. Instead, such lysine becomes toxic to the<br />

cells and causes ahnnrmal morphology, cell division, and loss <strong>of</strong> viability. Such<br />

abnormalities mav serve as a model lo sludv the mechanism <strong>of</strong> hyperlysinemia, a<br />

severe metabolic disorder for I:hinr catabolism in children.<br />

G.F. Bills and J.D. Polishook. I4erck Sharp 6 Dohme<br />

Research Laboratories, P.O. Box 2000, Rahvay, NJ<br />

07065.<br />

Kicr<strong>of</strong>ungi from Carpinus caroliniana.<br />

This studv is an attempt to characterize the fungal<br />

flora inhabiting the bark <strong>of</strong> Carpinus caroliniana<br />

(<strong>America</strong>n Hornbeam, Ironwood). Trees were sampled<br />

from various sites in central New Jersey. Ten trees<br />

were selected at each site. From each tree, 24 one<br />

cm bark discs were removed. The bark discs were<br />

surface-sterilized and were distributed onto three<br />

isolation media. Colonies <strong>of</strong> fungi were alloved<br />

to develop and then transferred to slants for<br />

enumeration and identification. Thus far we have<br />

examined nearly 900 bark discs from 40 trees and<br />

recovered over 60 species <strong>of</strong> fungi. As expected, the<br />

£lor6 is dominated by common genera <strong>of</strong> Hyphomycetes.<br />

however a suprisingly high proportion <strong>of</strong> the isolates<br />

are Coelomycetes. A few Basidiomycetes were recovered<br />

with our method. A comparative analysis <strong>of</strong> the<br />

differences in species diversity and the frequencies<br />

<strong>of</strong> species recovered among individual trees, among<br />

different sites, and among isolation media is<br />

presented.<br />

M. BLACKWELL and D. IVILLOCH. Department <strong>of</strong> Botany. Lwisia~<br />

State University. Baton Rouge, LA 70803, and Department <strong>of</strong><br />

Botany. University <strong>of</strong> Toronto, loronto, Ontario M5S 1A1.<br />

Dispersal biology <strong>of</strong> Stvlowse m.<br />

Stvlow~e S.W. UooG, previously repnrted only trm the<br />

tyw local ity, Derbyshire, U.Y., is camon in noose c~ng at<br />

severe. La~dian localities. It was present within 2-6 aays <strong>of</strong><br />

incubarior, in all <strong>of</strong> the dung sanples examined. In a field study<br />

condrcted in Sept-r 1989, S. a m l a capilliconidia wre f d<br />

attached to phoretic mites <strong>of</strong> dung beetles more <strong>of</strong>ten than spores<br />

<strong>of</strong> any other species. Dispcrsai is similar to that reported for<br />

secondary capilliconidia <strong>of</strong> Basidiobolus spp. In mired cultures<br />

on agar. the mbs. Sawinia so., is an imortant prey organism<br />

for S. anmala. The fasci~ting amoeba has a presurptive phoretic<br />

stage that elmgates and sdheres to any objects that contact it.<br />

Although re have not been able to distinguish the amebae on<br />

trapped mites, ue assure that they here as do the cspillicMidia<br />

with which they are intersprred on the dvlg surface. Amebae are<br />

able to uithstand desiccation on cover glass shards for at least<br />

72 hrs. providing circumtantial evidence that they could survive<br />

disprsat thrqn air attached to the phoretlc mites. Thus.<br />

direct dispersal for both predator and prey nay ensure a food<br />

source for S. anomale in new substrates.<br />

M. BLACKYELL', J.Y. SPLTA~ORA~, D. MLLOCH~, and J.Y. TAYLOR',<br />

Deparlmmt <strong>of</strong> Botany. Louisiana State University, Baton Rouge, LA<br />

70803 , Departmyt <strong>of</strong> Botany, University <strong>of</strong> Tormto, Toronto,<br />

Ontario MSS 1A1 , and Departrnf <strong>of</strong> Plant Science, University <strong>of</strong><br />

California, Berkeley, CA 94RO .<br />

Ww evidence fro. an amrph for the renwal <strong>of</strong> Pyxidiwhora frm<br />

the Hypareales.<br />

Placement <strong>of</strong> Pyxididore Bref. 6 lav. in the Hypocreales alusys<br />

has been suspect. Early deliquescent ascl and absence <strong>of</strong> apical<br />

paraphyses are mt typical <strong>of</strong> the ordcr. Recognition <strong>of</strong> these<br />

differences led Arnold to prgase the new fmity Pyxidiwhoraceae<br />

for the genus and to suggest a relationshtp with the<br />

Melanosporaceae. Lurc(qvist accepted the fmily and suggested that<br />

it is misplaced in the Hypocreales. Most recently, von Arx and<br />

van der Walt placed the Pyxidiophoraceae in the Ophiostaateles,<br />

partially on the basis <strong>of</strong> a anamorpl. rwrted for several<br />

species. In a discussion <strong>of</strong> the relationships <strong>of</strong> PyxidioMora,<br />

Blackwell and Malloch chose nor to e@esize the evidence <strong>of</strong><br />

anamorphs because the cwmctions Mere mt proven<br />

conclu~ively. However, a presuwtive synmnatous anamorph <strong>of</strong><br />

Pyxic!iomora sp. has been discovered that is characterized 4'<br />

holoblastic conidia an percurrent or synPodial proliferation, a<br />

tm not k m in the hyvocreales. Although similarity <strong>of</strong><br />

cultures established from the conidia and ascospore products<br />

supports the ccnnution, neither culture prodxed s-te or<br />

perithecia. Because <strong>of</strong> the imortance <strong>of</strong> veritying the existence<br />

<strong>of</strong> a non-hypocrealean ansmorph tyue in Pyxidiophora, we used<br />

mother appmsch to obtain cvidmsr <strong>of</strong> the correction. Primer<br />

directed nplificat ion <strong>of</strong> nuclear encoded ribosansl RUA genes by<br />

the polyrrrase chain reaction and direct DNA squcncing allowed<br />

caparison <strong>of</strong> the two cultures. About LOO bases in the highly<br />

conserve0 rDNA were identical in the tw cultures. The 300 bases<br />

re ermined in the internal tramcribed spacer regions, k m to<br />

be variable in f-i, were also icentical. Molecular widem<br />

sqqmrts the canection, and ue cmsider the mnmmrph to be that<br />

<strong>of</strong> Pyxidiochora sp. Thus, sdditimnl amrph evidence to exclude<br />

Pptidiochora trrm the Hypocreales is provided.<br />

L. D. Boeck. Lilly Research Laboratories, Lilly<br />

Corporate Center, Indianapolis, IK 46285.<br />

ti l<strong>of</strong>ungin, a new semi-synthetic anti -6andida<br />

antibiotic from Aspergillus.<br />

iCandida is an important human pathogen for whose<br />

ltreatment few agents are available. In additi,on,<br />

!those antibiotics that are clinically effective are<br />

pi kely to exhibit host toxicity. Aspergillus species<br />

ihave been shown to produce several lipopeptide anti-<br />

lbiotics that likewise possess activity vs. Candida.<br />

These lipo~eptides, which include Echinocandin 6<br />

;(ECB), appear to act on various target sites and are<br />

lalso likely to exhibit host toxicity. However, minor<br />

changes in their fatty acid acyl chain substituents<br />

ihave been shown to exert major changes in activity<br />

:and/or toxicity. Successful studies previously<br />

:conducted at Lilly for removal <strong>of</strong> an acyl group from<br />

la related lipopeptide possessing gram positive<br />

;activity, A21978C, led to the discovery that a


similar process could be applied to ECB. Therefore,<br />

several Aspergillus species obtained from an ongoing<br />

soil screen,were used to produce ECB by fermentation.<br />

ZCB was subsequently isolated and partially purified,<br />

:after which bioconversion to the polypeptide nucleus<br />

was accomplished by deacylating with Actinoplanes<br />

ut3hensis. The bioinactive peptide nucleus <strong>of</strong> ECB<br />

was then isolated and chemically reacylated with<br />

.various acyl analogs. An octyloxybenzoyl acyl group<br />

was shown to confer a favorable therapeutic index.<br />

This promising new compound, known as cil<strong>of</strong>ungin, is<br />

currentfy on clinical trial.<br />

;E.W.A. Boehm and D.J. McLaughlin. Cereal Rust Labora-<br />

tory, USDA-ARS, and Department <strong>of</strong> Plant Biology, Uni-<br />

bersity <strong>of</strong> Minnesota, St. Paul, MN, 55108.<br />

An ultrastructural karyotype for Eocronartium w-<br />

cola.<br />

Definitive karyotypes for small fungal nuclei are<br />

best obtained at meiotic pachytene, using threedimensional<br />

reconstructions <strong>of</strong> synaptonemal complexes.<br />

Paciytene nuclei in Eocronartium muscicola, a simple<br />

scptate auricularioid moss parasite, related to the<br />

Uredinales , were preselected prior to serial sectioning<br />

for TEN using epifluorescence microscopy. Seventeen<br />

synapsed homologues were resolved in each <strong>of</strong><br />

four fully reconstructed nuclei originating from two<br />

differe~lt moss hosts. Five <strong>of</strong> the seventeen chromosolnes<br />

were cross correlated among the four nuclei<br />

based on calculated length and centromeric index. One<br />

chromosome cf ~haracteristic lengt+ and centromeric<br />

index was found to be associated with the spindle<br />

pole body (Spa). This is the first report <strong>of</strong> a synaptonemal<br />

complex in association with a fungal SPB<br />

and may relate to the heterochromatin found to subtend<br />

the SPE in non-pachytene stages.<br />

S.H. BOYUCHKO and J.P. TEWARI. Department <strong>of</strong> Plant<br />

Science, University <strong>of</strong> A1 berta, Edmonton, A1 berta,<br />

Canada T6G 2P5. Variation among barl ey cul ti vars<br />

to VA mycorrhizal colonization.<br />

The VA mycorrhizal fungi are generally be1 ieved to be<br />

host non-specific, but certain host preferences are<br />

known to exist. Field and greenhouse trials were<br />

therefore conducted to determine whether various VA<br />

mycorrhizal fungi show variations in colonization <strong>of</strong><br />

the roots <strong>of</strong> barley cultivars. Additionally, the<br />

growth benefits accrued to the barley cultivars were<br />

measured. Field experiments did not show any<br />

significant differences in levels <strong>of</strong> root<br />

colonization by indigenous Glomus spp. in 22 barley<br />

cultivars over a 3 year period. However, greenhouse<br />

studies, in which 8 barley cultivars were inoculated<br />

with Glornus dimor~hicum, G. intraradices, or G.<br />

mosseae, indicated that certain barley cultivars are<br />

colonized to a greater extent by VA mycorrhizal fungi<br />

than others. Glomus intraradices and $. mosseae<br />

generally colonized barl ey more than 5. dimor~hicum.<br />

Also, 4 <strong>of</strong> the 8 barley cultivars exhibited greater<br />

yield and seed size when inoculated with E. mosseae<br />

and G. intraradices over the controls, but not with<br />

- 6. dirnor~hicum. It therefore appeared that barley<br />

cultivars varied in their susceptibilities to VA<br />

mycorrhizal colonization and that colonization and<br />

growth benefits exhibited in the plants was also<br />

gcvernec oy the VA mycorrhizal species present in the<br />

soil.<br />

Harold H. Burdsall. Jr..and Mark T. Banik. Center<br />

for Forest Mycology Research. USDA-Forest Products<br />

Laboratory. Madison. WI. Cultural characteristics<br />

<strong>of</strong> the North <strong>America</strong>n Species <strong>of</strong> Armillaria in<br />

culture.<br />

Several tissue or multisporous cultures from each<br />

<strong>of</strong> the nine North <strong>America</strong>n species <strong>of</strong> the<br />

Armillaria mellea complex and A. tabescens were<br />

compared on a 1.5 percent malt extract. 2 percent<br />

agar medium. Cultures were grown at 12. 16. 20.<br />

24. 28. 32 and 36 C. After four weeks all cultures<br />

were diametrically measured and molrphological<br />

characters recorded from those grown at 24 C.<br />

Except for NABS VII cultures <strong>of</strong> all species <strong>of</strong> the<br />

--<br />

A. mellea complex grew at similar rates at all<br />

temperatures. NABS VII grew substantially faster<br />

at 32 and 36 C. Isolates <strong>of</strong> all species. except<br />

NABS I11 and IX and A. tabescens. were culturally<br />

consistent morphologically. NABS VI was the most<br />

distinct culturally possessing a mostly vhite.<br />

fluffy culture mat. Most other species were<br />

reddish-brown and appressed. NABS I1 had a<br />

distinctive feathery edge and NABS V stained the<br />

agar reddish-brown. NABS I and X were<br />

undistinguishable. both possessing extensive<br />

reddish-brown crustose area in the center <strong>of</strong> the<br />

colony with a hyaline margin. NABS VII cultures<br />

generally were heavily zonate and stained the agar<br />

reddish-:.mwn. Lack <strong>of</strong> consistency within some<br />

species M opposed to others may indicate a lack <strong>of</strong><br />

integrity <strong>of</strong> these species.<br />

C. BRAD=. P. WOOD, W. BLACK., B. WARNS and C.<br />

NEAR. hlycotech Bioproducts, Inc., P.O. Box 4113, Butte,<br />

MT 59702.<br />

De\,elopment <strong>of</strong> Lieauveria bassiuna rnycoinsecticides.<br />

Production techno103 is a key element in developing<br />

rnycoinsecticides, not only in evaluating economics, but also<br />

in strain selection, formulation, application methods, and<br />

regulato~ compliance.<br />

Production <strong>of</strong> B. bassiana conidia has been developed using<br />

solid substrate culture with yields <strong>of</strong> 2-5 X 10'%0nidia per<br />

kg <strong>of</strong> substrate. The product is a stable dry powder suitable<br />

for a number <strong>of</strong> formulation options.<br />

Fifty isolates have been compared for virulence and conidia<br />

production in developing mycoinsecticides for grasshopper<br />

and ,vsy moth control. Conidia production efficiency is an<br />

important criteria in strain selection. Liquid spray and bait<br />

formulations have been tested in laboratory. outdoor cage<br />

and field trials for rassho per control at application rates<br />

1B 1B<br />

equivalent to 10 to 10 conidia per ha, In cage trials<br />

80-100% mortality was obtained with 1012 and 1013 conidia<br />

per ha equivalent.<br />

Formulations and application methods designed for ,vsy<br />

moth control in urban and suburban areas have been<br />

developed and tested in laboratory and field trials. Mortality<br />

rates <strong>of</strong> 80- 10070 have been obtained in laboratory trials, and<br />

63% in initial field trials using economical application rates.<br />

Production should be integrated at a very early stage in<br />

orams.<br />

mycoinsecticide develop men^ pro,


B. E. CALLAK. Pacific Forestry Centre, 506 West<br />

Burnside Road, Victoria, B.C. V8Z 1M5 CANADA.<br />

Evaluation <strong>of</strong> taxonomy and biogeography <strong>of</strong> the<br />

Xylariaceae using cultural characters and anamorphs.<br />

The Xylariaceae is a large and complex cosmopolitan<br />

family whose taxa have historically been delimited by<br />

stromatal color, gross morphology and habit. The<br />

f om-genera and habit <strong>of</strong> xylariaceous anamorphs are<br />

<strong>of</strong>ten key characters currently used to delimit genera<br />

and are usually the most reliable criteria for<br />

placing intermediate forms into the appropriate genus.<br />

Cultural and anamorphic features have also been useful<br />

in identifying groups <strong>of</strong> closely related taxa. These<br />

features help to determine in geographically separated<br />

collections if variations in stromatal morphology<br />

and spore size are reflected in the morphology <strong>of</strong> the<br />

conidial state.<br />

Xylariaceous taxa occur with greatest frequency and<br />

diversity in the tropics. Recently, several large<br />

collections <strong>of</strong> tropical specimens have been examined<br />

and cultured. Comparisons <strong>of</strong> temperate and tropical<br />

~collections, and occurence <strong>of</strong> taxa in widely<br />

geographically separated regions dl1 be discussed.<br />

L. M. m. Department <strong>of</strong> Plant Pathology,<br />

Washington State University, Pullman, WA 99164-<br />

6430. Observations on a Cvstodendron species from<br />

Vaccinium.<br />

Cvstodendron is a poorly known genus based on C.<br />

drvophilwr.. It is characterized by sessile,<br />

penicillare clusters <strong>of</strong> conidiogenous cells with<br />

well-developed collarettes and minute, globose<br />

conidia. Cvstodendron has been connected to<br />

teleomorphs in the Helotiales but little else is<br />

known about them. Cvstodendron sp. on stems <strong>of</strong><br />

wild and cultivated Vacciniwn cormbosun in New<br />

Jersey was indistinguishabie from the type <strong>of</strong> C.<br />

drvo~!illwn on host tissue. In culture, however,<br />

the fungus is morphologically more similar to<br />

phialoce~hala dimorahos~ora. The Cvstodendron from<br />

Vaccinim. and 1. dimor~hosoora both produce<br />

coni~iophores <strong>of</strong> variable length, clusters <strong>of</strong><br />

conidiopenous cells and dimorphic conidia, with the<br />

firsc-formed conidium ovoid in shape and subsequent<br />

co~idia globosh. This is the first report <strong>of</strong><br />

dimorphic conidia in Cvstodendron. Based on the<br />

morphologicai similarity between the two genera,<br />

Aebi in 1972 proposed that J'hialoce~hala be placed<br />

in synonymy with Cvstodendron. Evidence from<br />

cultural studies <strong>of</strong> Cvstodendron and J'hialoce~hala<br />

is presented to support the maintenance <strong>of</strong><br />

J'hialoce~hala and Cvsrodendron as distinct genera.<br />

K.M.T. CASON' and J.K. ROBERTSZ. Departments <strong>of</strong> 'Plant Pathology<br />

and 'Biochemistry. University <strong>of</strong> Georgia, Athens, GA 30602.<br />

DNA restriction fragment pnlynorphisms lor identification <strong>of</strong> aml<br />

powdery mildew isolates (Bhmmia gmminir).<br />

The powdery mildew fqus Bherio gmminis (=E?siphc gruminis), an<br />

important plant pathogen <strong>of</strong> cereals, has long been known to exhibit<br />

biolopical speaalization for host species and host cultivar. Availability <strong>of</strong><br />

rapid, precise methods for identification <strong>of</strong> subspecies based on the<br />

anamorph which is the most common morph encountered in nature, would<br />

aid in providing accurate data reparding the epidemiology, host-parasite<br />

relationship, and systematics <strong>of</strong> this funp. Phenetic analysis <strong>of</strong> three<br />

formae speciales (f.sp hordei from barley, f.sp. fririci from wheat, and tsp.<br />

bromi from bromus carhonicus). and l3 races <strong>of</strong> the barley mildew showed<br />

that rnorpholw <strong>of</strong> the anamorph cannot be used to identify subspecies.<br />

Lonsequeotly, vanous DNA probes were tested in Southern analysis <strong>of</strong> total<br />

pnomic DNA lo determine whether hybridization patterns were<br />

characteristic for particular formae spedales and/or races. A 6 kb fragment<br />

that contained the rDNA penes from B. m inis f.sp. hordei (BGH) CR3<br />

was cloned and used as a probe to identify restriaion fragment length<br />

polymorphisms (RFLPs) in DNAs from the formae speciales and races<br />

indicated previously. Restriction patterns obtained by digestion <strong>of</strong> DNA<br />

with 18 different restriction endonucleases showed no significant<br />

plymorphisms in the rDNA pnes from the races <strong>of</strong> the barley powdery<br />

mildew. However, the rDNA restriction fragment phenotypes <strong>of</strong> formae<br />

speciales exhibited sienificant polymorphisms for digestions with various<br />

restriction enzymes including Smal (Xmal) and EcoRI. Other probes were<br />

tened including the 6-tubulin gene from BGH-CR3, hsp7O from soybean,<br />

random clones from a BGH CR3 library, and mitochondrial genes from<br />

Neurospora crassa (mt-mochrome b, mt-cyrochrome oxidase, mt-5s<br />

rDNA). Chararueristic RFLPs were detected for the formae speciales with<br />

rDNA genes, hsp70, mt-qlochrome oxidase and mt-25s rDNA. Variations<br />

in restriction patterns for races <strong>of</strong> the barley mildew were obtained with<br />

hsp70, ml-cvtochrome oxidase, and mt-2.5s rDNA.<br />

M. A. CASTELLANO Forestry Sciences Laboratory, PNW<br />

Forest Research Station, 3200 Jefferson Way, Corvallis,<br />

OR 97331.<br />

Biogeography <strong>of</strong> gastroid Basidiomycotina and<br />

Ascornycotina.<br />

Most gastroid (truffles and false-truffles) Ascomycotina,<br />

Basidiomycotina, and sporocarpic Endogonaceae form<br />

mycorrhiza. They depend primarily on various mammals<br />

for spore dispersal. Biogeography <strong>of</strong> truffles and false-<br />

truffles is influenced by the physiological habit <strong>of</strong> the<br />

fungus (mycorrhizal or saprophyte), global climate<br />

change, topography, continental drift, and host specificity.<br />

The unique triparite association <strong>of</strong> host, fungus and<br />

mammal rnycophagist reduces the opportunity for<br />

migration. The rnycogeography <strong>of</strong> the northern and<br />

southern Hemispheres <strong>of</strong>fers an interesting array <strong>of</strong><br />

similar and dissimilar fungi for comparison.<br />

R. J. Chacko, G.J. Weidmann and D.O. TeBeest, Dept. <strong>of</strong><br />

EtPaFhology, Univ. <strong>of</strong> Arkansas, Fayettwille, AR<br />

72701<br />

Mycelial analysis <strong>of</strong> Heterokoryotic colonies <strong>of</strong> Colle-<br />

totrichm ploeosporioides f. sp. aeschynanene.<br />

?he potential for genetic exchange via parasexual<br />

means in Colietotrichum gloeosporioides f. sp. aeschv-<br />

nomene (GA) was inves tiga tea using auxotrophic mu t-<br />

ants. CGA isolates from Arkansas and Louisiana were<br />

paired on minimal media to generate heterokaryons.<br />

Heterokaryons exhibited a slower growth rate and poor<br />

sporulation. Conidia collected from heterokaryotic<br />

colonies segregated as parental types when tested on<br />

appropriate selective media. Plate cultures <strong>of</strong> heter-<br />

okaryotic colonies 2-3 weeks old were analyzed to de-<br />

termine the pattern <strong>of</strong> heterokaryotization within the<br />

colony. Eight radii were selected fran test colonies<br />

and 1 sq. inn mycelial blocks were transferred to se-<br />

lective media for analysis. Sequential mycelial trans-<br />

fers from the outer margin to the center <strong>of</strong> the colony


were transferred to minimal plates from two radii.<br />

From the remaining six radii three mycelial blocks<br />

from the outer, middle and central portions <strong>of</strong> the<br />

colony were .transferred to minimal media and minimal<br />

media supplemented with one <strong>of</strong> the parental require-<br />

ments. Results indicate that heterokaryotic regions<br />

do not extend beyond the central portion <strong>of</strong> the colony<br />

In sane cases both auxotrophic canponents were uni-<br />

formly distributed in the outer region <strong>of</strong> the colony.<br />

In other heterokaryons only one parenk was found at<br />

the periphery <strong>of</strong> the colony. 'Ihis study suggests that<br />

the auxotrophic portion <strong>of</strong> the colony is nutritionally<br />

supplemented by a smaller prototrophic region at the<br />

center <strong>of</strong> the colony.<br />

T.E. CHASE. J. TAYLOR. F.W. COBB. JR.. P.T. SPIETH,<br />

and W.J. OTROSINA. University <strong>of</strong> California.<br />

Berkeley 94720 and USDA-Forest Service Pacific<br />

Southwest Forest and Range Experiment Station.<br />

Berkeley. CA 94701.<br />

Mitochondria1 DNA differences among biological<br />

species <strong>of</strong> Heterobasidion annosum.<br />

H. annosum, a basidiomycete root- and butt-rot<br />

fungus <strong>of</strong> conifers. contains several biological<br />

species (intersterility groups). Previous mating<br />

tests and isozyme studies (which assess primarily<br />

nuclear encoded genes) indicate that the S and P<br />

groups in the western United States have undergone<br />

a high degree <strong>of</strong> genetic divergence and that there<br />

is no gene flow between them. In order to assess<br />

the cytoplasmic genome, we analyzed mitochondria1<br />

DNA restriction fragment length polymorphisms<br />

(mtDNA RFLPs) with a rapid screening method<br />

employing the Hae 111 restriction endonuclease.<br />

RFLP patterns for S group strains from North<br />

<strong>America</strong> were clearly different from P group strains<br />

from North <strong>America</strong>. In addition. differences in<br />

Rm9 patterns exist between European and North<br />

<strong>America</strong>n S group strains. These results are<br />

consistent with our earlier studies based on<br />

nuclear genes. both <strong>of</strong> which demonstrated that the<br />

biological species <strong>of</strong> K. annosum represent well<br />

separated gene pools.<br />

T.E. CHASE and R.C. ULLRICH. Plant Pathology<br />

Dept.. University <strong>of</strong> California, Berkeley 94720<br />

and Botany Dept.. University <strong>of</strong> Vermont.<br />

Burlington 05405.<br />

"Illegitimate" mating in Heterobasidion annosum.<br />

In previous studies we showed that intersterility<br />

in H. annosum is regulated by five genes.<br />

designated Vl+/Vl-. V2+/V2-. V3+/V3-. S+/e,<br />

P+/k.<br />

Any two homokaryotic strains are<br />

interfertile (able to form dikaryons) if they are<br />

homoallelic for + alleles at one or more <strong>of</strong> these<br />

loci and also carry compatible mating-type<br />

alleles. Cases in which intersterile pairings<br />

give rise to putative dikaryons are reported<br />

here. Such "illegitimate" mating occurs<br />

inconsistently, but is more frequent when<br />

pairings are incubated for a prolonged (30 day)<br />

period rather than the normal 10 day period prior<br />

to the routine subculturing step which is part <strong>of</strong><br />

the mating protocol. Analysis <strong>of</strong> progeny derived<br />

from an illegitimate mating suggest a genetic<br />

model in which parasexuality may play a role in<br />

generating nuclei containing recombinant<br />

genotypes which are interfertile and compatible<br />

with one <strong>of</strong> the progenitor nuclei. Illegitimate<br />

mating thus represents a special case <strong>of</strong><br />

intersterile and interfertile mating behavior.<br />

because the dikaryons resulting from such events<br />

contain two genomes with + alleles in common at<br />

at least one <strong>of</strong> the five loci. Ability to engage<br />

in illegitimate mating is a strain-specific<br />

characteristic but does not appear to be<br />

inherited as a simple Mendelian trait.<br />

A. W. CHEN. Russell Res. Ctr. PPRU. P.O. Box 5677.<br />

Athens, CA 30613. Transition to reproduction in<br />

Fanodema Jucidum and other basidiomycetes.<br />

Six stages (grovth in vegetative medium, grovth in<br />

fruiting medium, transition to basidiocarp primor-<br />

dium formation, stipe formation, growth <strong>of</strong> pileus,<br />

and tube & spore formation) are identified in G.<br />

lucidum during transition to sexual reproduction.<br />

Cultures continue to grow vegetatively, or only<br />

abortive fruiting bodies (vithout tube & spore for-<br />

mation) will be obtained if proper cultural parame-<br />

ters are not maintained. These parameters include<br />

medium components (carbon source, C/N ratio, thia-<br />

mine, pH and texture), and abiotic factors for<br />

incubation (temperature, light/darkness. COJventi-<br />

lation, and moisture). Methodology on fruiting in-<br />

duction in s. lucidum is reviewed. Usually shifting<br />

from groving inoculum or spawn in vegetative medium<br />

to fruiting medium containing more complex carbohy-<br />

drates is involved. Of critical importance are: 1)<br />

transition to basidiocarp-primordium formation, and<br />

2) transition to tube h spore formation. Damaging or<br />

killing cells in fruiting cultures can induce pri-<br />

mordia or tube & spore formation. When vorking vith<br />

un-defined and heterogenous fruiting media, such as<br />

vood or sawdust, and bran or corn meal, or using<br />

induction techniques vith no specific effects, the<br />

results are not always consistent. The underlined<br />

processes during transition to basidiocarp formation<br />

(storage and utilization <strong>of</strong> energy sources, change<br />

<strong>of</strong> mycelial growth pattern, light induction, lipid<br />

synthesis, enzyme activities and ultra-structural<br />

studies on tube and spore formation) are selectively<br />

reviewed including other basidiomycetes.<br />

CHD-CHOU, 2. -Q. AN, J. 1. HENDRIX, Q.<br />

ZKAI, and H. R. BIEGEL. Department <strong>of</strong> Plant<br />

Pathology, University <strong>of</strong> Kentucky, Lexington<br />

40546.<br />

Effect <strong>of</strong> the Acremonium endophyte on<br />

endogonaceous mycorrhizal fungi reproducing<br />

on tall fescue.<br />

Soil samples taken from field plots planted<br />

to tall fescue (cv. Ky 31) with low or high<br />

levels <strong>of</strong> the hcremonium coenowhialum<br />

endophyte were assayed for endogonaceous<br />

propagules by an MPN bioassay procedure.<br />

Soil from low-endophyte plots contained more<br />

propagules and species than soil front high-<br />

endophyte plots. Pure cultures <strong>of</strong> one<br />

isolate <strong>of</strong> Glomus mosseae and two isolates


<strong>of</strong> E. macrocarwum were used to inoculate<br />

endophyte-infected or -free fescue seedlings<br />

growing in the greenhouse in sand fertilized<br />

with a high or low rate <strong>of</strong> slow-release<br />

fertilizer. Colonization and reproduction<br />

by E. rosseae, but not the E. pacrocamum<br />

isolates, was inhibited by the high rate <strong>of</strong><br />

fertilizer. The G. mosseae and one <strong>of</strong> the<br />

-<br />

G. pacrocarwum isolates reproduced better on<br />

the endophyte-free fescue than on endophyte-<br />

infected. The other isolate <strong>of</strong> E.<br />

macrocarwum did not reproduce well on either<br />

fescue seed source, although roots were<br />

colonized.<br />

J.D. CLARK School <strong>of</strong> Biological Sciences,<br />

University <strong>of</strong> Kentucky, Lexington, KY 40506.<br />

Didymium iridis mating systems: partial<br />

compati bi li t y between mating series.<br />

k Oidymium iridis isolate (GB 1) from<br />

Bristol England was crossed to Colllns'<br />

standard mating allele testers to determine<br />

its relationship to the mating series.<br />

When paired to the Central <strong>America</strong>n series<br />

only a few plasmodia were produced in<br />

repeated crossings i n 4 <strong>of</strong> the 28 possible<br />

combinations. These plasmodia produced<br />

sporangia containing many non-viable spores<br />

which displayed skewed mating type segrega-<br />

tion ratios. When paired with clones from<br />

the 3 non-interbreeding isolates, the GB 1<br />

clones did not cross with the Ga 1 and Fla 1<br />

isolates but did produce plasmodia i n 3 <strong>of</strong><br />

the 4 possible combinations with the Pan 4c<br />

isolate. These plasmodia also produced<br />

spores with low viability and poor segrega-<br />

tion ratios. On the other hand, pairings<br />

with the Appalachia series produced plasmod-<br />

ia in most replica crosses <strong>of</strong> all 8 possible<br />

combinations. These plasmodia generally<br />

produced viable spores and normal segregation<br />

ratios. Most g. iridis heterothallic iso-<br />

ilates have mating type alleles which are com-<br />

patible with only a single geographically<br />

restricted mating series. The GB 1 isolate,<br />

however, is partially compatible with 3<br />

separate series although it is closest to the<br />

Appalachia series in terms <strong>of</strong> compatibili ty.<br />

S. A. CLARY and M. E. S. HUDSPETH. Dept. Biological<br />

Sciences, Northern Illinois University, DeKalb, IL<br />

60115-2861<br />

Nucleotide sequence <strong>of</strong> Phytophthora mitochondrial<br />

DNA: Sequence <strong>of</strong> the apocytochrome b and ATP sy-<br />

thase subunit 9 region.<br />

Seven mitochondrial genic loci have been previously<br />

established in Phytophthora megasperma 695T.<br />

These include subunits for cytochrome c oxidase<br />

( ~ 1 2, . 3), apocytochrome b (cob), subunit 9 <strong>of</strong><br />

AT? svnthase (atp9), and the small and large ribosoza:<br />

RNAs (E, s). The validity <strong>of</strong> the -9<br />

locus was questionable as, unlike the other loci,<br />

it failed to hybridize with ascomycetous probes,<br />

and was localized by an unsequenced Saprolegnia<br />

probe. Prior DNA sequence data <strong>of</strong> cox1 and 3 2<br />

have indicated the probable use <strong>of</strong> the universal<br />

genetic code in Phvtophthora.<br />

We have cloned and sequenced a 3.9Kb g R I<br />

fragment <strong>of</strong> the 6951 mtDKA containing the cob and'<br />

- atp9 loci. This region contains four open reading<br />

frames (ORFs). Two ORFs shox high degrees <strong>of</strong> predicted<br />

amino acid homology with ascomycetous cob<br />

and 9 9 loci. Whether the mitochondrial =9is<br />

functional, as in Saccharomyces, or silent, as in<br />

filamentous ascomycetes is undetermined. One <strong>of</strong> the<br />

remaining ORFs is an inverted copy <strong>of</strong> a sequence<br />

directly upstream <strong>of</strong> ~ 2 All . four ORFs are transcribed<br />

from the same DNA strand, but opposite to<br />

that <strong>of</strong> ~ l ~ , 2 and , the other copy <strong>of</strong> the repeated<br />

ORF. A search for homologies <strong>of</strong> the unkno.wn<br />

ORFs to other mitochondrial genes is underway.<br />

u. Department <strong>of</strong> Biology, Indiana<br />

University, Bloomington, IN 47405.<br />

Population Genetics and Host Range Expansion <strong>of</strong><br />

Atkinsonella hv~oxvlon (Clavicipitaceae).<br />

Shifts in host range represent the ultimate<br />

starting point for most host-parasite associations<br />

yet this important process has received little<br />

attention compared to research on variation in<br />

compatibility within prexisting species<br />

combinations. ptkinsonella hv~oxvloq, classified<br />

with endophytic fungi in the tribe Balansieae, has<br />

extended its host range from two species <strong>of</strong><br />

panthonia over much <strong>of</strong> eastern North <strong>America</strong> to two<br />

additional panthonia species occurring on montane<br />

granitic outcrops in the southern Appalachians near<br />

Highlands, NC where all four host species occur.<br />

Preliminary data from seedling inoculations<br />

indicate that the basis <strong>of</strong> host range expansion is<br />

genetic changes in fungal populations. Isozyme<br />

studies have revealed that isolates <strong>of</strong> the fungus<br />

from the new hosts represent only a few genotypes.<br />

Relative fitnesses <strong>of</strong> infected versus uninfected<br />

host plants suggest that Atkinsonella is more<br />

pathogenic on the new hosts. Evolutionary changes<br />

in isolates from the new hosts are facilitated by<br />

differences in host flowering times, minimizing<br />

gene flow between isolates from the new and old<br />

hosts. Crosses between isolates from the new and<br />

old hosts have been attempted to elucidate the<br />

nature <strong>of</strong> genetic control <strong>of</strong> host range.<br />

Evolutionary changes in Atkinsonella populations<br />

infecting the new hosts may represent incipient<br />

speciation.<br />

BRUCE J. COCHRANE, REX T. NELSON, BIENVENIDO G.<br />

YANGCO, AND DIANE TE STRAKE. Department <strong>of</strong> Biology and<br />

College <strong>of</strong> Medicine, Univ. <strong>of</strong> S. Florida, Tampa. FL. 33620. rDNA<br />

polymorphisms and phylogenetic relationships in Baridiobolus.<br />

The genus Basidiobolus (Zy~omycotina;<br />

Entomophthorales) is a<br />

widespread saprobe that ou;rsionally causes mycoses in man and other<br />

vertebrates. While as many as ei~ht species <strong>of</strong> the genus have been<br />

proposed, our analyses <strong>of</strong> both isozye and rDNA polyfnorphisms


support only two <strong>of</strong> these species (B. ranurunl and B. microsporus).<br />

However, there is extensive heterogeneity among Nonh <strong>America</strong>n<br />

saprobic isola!es that. based upon parsimony analysis, separates them<br />

from human and European saprohic isolates. We have examined<br />

additional isolates. using hoth RFLP analysis and sequencing <strong>of</strong> PCR<br />

products obtained from amplification <strong>of</strong> the internal transcribed spacer<br />

region <strong>of</strong> rDNA gcnes. These analyses suggest that, in contrast to<br />

isolates ohtained from the New World. those from the Old World are<br />

homogeneous. In light <strong>of</strong> these data, we suggest that more extensive<br />

analysis will he required to clarify the taxonomy-<strong>of</strong> the genus, and to<br />

establish whether geopraphic patterns <strong>of</strong> human infection are reflective<br />

<strong>of</strong> genetic differentiation within Basidioholus, or whether they are<br />

assoc~ated with cultural or social laclors.<br />

MONICA L. CONVERSE and T. PI. WlrlILL. De~artment <strong>of</strong><br />

Biology; SUNY College at Oswego, Oswego, NY 13126.<br />

Electron microscopy <strong>of</strong> mitosis during sporangial<br />

development in Mucor mucedo (Mucorales).<br />

Fungi in the tlucorales reproduce asexually by forming<br />

spores within sporangia. Sporangial development is<br />

accompanied by numerous mitoses prior to cleavage and<br />

sporogenesis. Sporangia <strong>of</strong> Mucor mucedo contain hun-<br />

dreds <strong>of</strong> spores, each with 20-30 nuclei, the products<br />

<strong>of</strong> mitosis. Nuclear division has been examined in<br />

W. mucedo, and the results confirm our understanding<br />

<strong>of</strong> the process in the Mucorales. In such fungi,<br />

mitosis is intranuclear, i.e., the nuclear envelope<br />

remains intact throughout the entire process <strong>of</strong> divi-<br />

sion. In K. mucedo, dividing nuclei possessed an<br />

intranuclear, microtubular spindle apparatus which<br />

developed between intranuclear spindle pole bodies.<br />

The spindle pole bodies were in the form <strong>of</strong> electron-<br />

opaque disks closely appressed to the inner nuclear<br />

envelope. During prophase, a short spindle apparatus<br />

appeared laterally within a nucleus, and lengthened<br />

while spindle pole bodies migrated toward polar posi-<br />

tions. Indistinct chromosomes apparently attached<br />

to the spindle microtubules, but did not align on a<br />

metaphase plate. Toward the end <strong>of</strong> mitosis, equal<br />

amounts <strong>of</strong> nucleolar material appeared to be located<br />

in the ends <strong>of</strong> dumbbell-shaped nuclei. Nuclear poles<br />

moved apart until daughter nuclei resulted from<br />

separation <strong>of</strong> the constricted envelope connecting<br />

the poles.<br />

M. COOKE , P. MOUTOGLIS, AND P. WIDDEN. Biology<br />

Dept. , ~oncordi'a University, 1455 de Maisonneuve<br />

West, Montreal .F.Q., Canada.<br />

VAM Fungi in a maple forest in the Laurentians.<br />

Rates <strong>of</strong> infeetion <strong>of</strong> maple roots and the occurrence<br />

<strong>of</strong> VAM spores In soil were surveyed durinq a single<br />

season in a maple forest in the Laurentians , close<br />

to the northern limit for sugar maples in Canada.<br />

The stand is currently suSject to acie precipitation<br />

with an average pH <strong>of</strong> 4.3.<br />

The data. shaw that both rates <strong>of</strong> infection and<br />

numbers <strong>of</strong> spores vary seasonally. The major<br />

internal structures in the maple roots were hyphal<br />

coils and vesicles, arbusciles bein9 only rarely<br />

observei. The major taxa present in the .soil 'as<br />

spores were species <strong>of</strong> .Giomus, ' Sclerocysfis<br />

rubiformis, an8 a spe'cies <strong>of</strong> Acalospora.<br />

S.C. CROAN and T.L.Highley. U.S. Department <strong>of</strong><br />

Agriculture. Forest Service. Forest Products<br />

Laboratory, One Gifford Pinchot Drive. Madison. WI<br />

53705-2398, U. S. A.<br />

Selection <strong>of</strong> Fungal Antagonists for Biological<br />

Control <strong>of</strong> the Blue Stain Fungus Ceratocystis<br />

coerulescens<br />

The objective <strong>of</strong> this study was to find a fungal<br />

antagonist that could be used to control blue stain<br />

in wood caused by Ceratocystis coerulescens. We<br />

studied interaction <strong>of</strong> C. coerulescens with the<br />

following fungi in dual culture on agar medium:<br />

white-rot basidiomycetes--Bjerkanderd adusta.<br />

Coriolus versicolor. Ganderma applanatum. Lentinus<br />

edodes. Phanerocheate chrysosporium. Phlebia<br />

brevispora. and Schizophyllum commune; brown-rot<br />

basidiomycetes--Antrodia carbonica. Coniophora<br />

puteana. and =a placenta, and one<br />

mold--Talaromyces flavus. Viability examination<br />

showed that all these organisms killed C.<br />

coerulescens. B. adusta not only killed the fungus<br />

but also decolorized the blue stain. C. uteana<br />

released an antibiotic-like substance :ha! inhibited<br />

the growth <strong>of</strong> C. coerulescens at a distance. The<br />

other fungi inhibited the growth <strong>of</strong> C. coerulescens<br />

only on contact. Our results indicate that blue<br />

stain can be controlled by fungal antagonists.<br />

D. CULLEN and S.F. COVERT. 1. Forest Products Labora-<br />

tory, One Gifford Pinchot Dr., Madison, k!I, 53705.<br />

2. Dept. <strong>of</strong> Bacteriology, University <strong>of</strong> Wisconsin,<br />

Madison. UI 53706.<br />

Heterologous protein expression in filamentous fungi.<br />

Recent research into heterologous gene expression<br />

in filamentous fungi has been prompted by two princip1,e<br />

factors: 1. The development <strong>of</strong> efficient gene<br />

transfer systems for several species, and 2. The<br />

ability <strong>of</strong> filamentous fungi to secrete copious<br />

quantities <strong>of</strong> protein in submerged culture.<br />

Aspergillus nidulans has been used as a model system<br />

for expression <strong>of</strong> commercial enzymes (bovine chymosinl<br />

232 pharmaceuticals (interferon; tissue plasminogen<br />

activator). Related species such as A. awamori, A,<br />

niger, and<br />

oryzae, and cellulolytic Trichoderma<br />

reesei strains have also been used. The advantages<br />

<strong>of</strong> filamentous fungi as expression systems relative<br />

to yeasts and prokaryotes will be discussed.<br />

K. J. C7YMMEK and K. L. KLOMPARENS. Department <strong>of</strong> Botany<br />

and Plant Pathology and Center for Electron Optics, Pesticide<br />

Research Center. Michigan State University, East Lansing, MI<br />

48824-1 31 1.<br />

The Ultrastructure <strong>of</strong> Ascosporogenesis in Thelebolus<br />

crustaceus using Cryo-techniques.<br />

Thelebolus crustaceus, a 5-12 ascal, 64-spored operculate<br />

discomycete, was examined using low temperature SEM and<br />

freeze-substitution TEM to determine morphological aspects<br />

during ascosporogenesis. Early in ascocarp development, the<br />

ascogonial coil was encompassed by ascogenous hyphae,<br />

resulting in a spherical mass. As the ascocarp matured, asci<br />

~ushed through the upper layers <strong>of</strong>-ascogenous hyphae and<br />

showed their prominent operculate tips. The young ascus<br />

shswea a diploid nilcleus and ciosely associated mitochondria in


the area <strong>of</strong> the ascus apex and proliferate vacuolation in the<br />

lower portions <strong>of</strong> the ascus. After meiosis I and II and the four<br />

subsequent mitoses, a pair <strong>of</strong> membranes, apparently derived<br />

from the fusion <strong>of</strong> numerous plasmalemmal invaginations.<br />

formed a cylinder around most <strong>of</strong> the ascus protoplasm. The<br />

double membrane invaginated to surround the individual nuclei<br />

and accompanying organelles, thus delimiting the ascospore<br />

initials. Wall material was deposited between the double<br />

membranes forming the ascopore wall. Other observations<br />

include the appearance <strong>of</strong> clusters <strong>of</strong> glycogen particles,<br />

several different types <strong>of</strong> cisternae, and small numbers <strong>of</strong><br />

microtubules running adjacent to the ascus and ascospore<br />

walls. Also, peculiar plasmalemmal invaginations were seen<br />

in the ascus, ascogonium, and ascogenous hyphae. These<br />

plasrnalemmal invaginations developed into ring-like<br />

structures which appeared to break <strong>of</strong>f and enter the<br />

cytoplasm. Eventually, the mature ascus ejected its<br />

ascospores in a single mass.<br />

T. W. DARMONO and H.H. BURDSALL. JR. Center for<br />

Forest Mycology Research, Forest Products<br />

Laboratory. Gifford Pinchot Dr.. Madison. WI 53705.<br />

A method for identifying mating types <strong>of</strong> single<br />

spore isolates in Armillaria mellea.<br />

We developed a method to distinguish the four mating<br />

type interactions in Armillaria mellea. Pairs <strong>of</strong><br />

monosporous isolates are grown 10 mm apart on oak<br />

wood extract (OWE) agar in petri plates in<br />

polyethylene bags. After 14 d incubation at room<br />

conditions. a strip. 2x35 mm. is cut across the two<br />

colonies perpendicular to the interaction zone.<br />

This strip, composed <strong>of</strong> parts <strong>of</strong> both colonies and<br />

the interaction zone, is transferred onto squeezed<br />

orange juice (SOJ) agar in petri plates. These are<br />

incubated in a polyethylene bag at room conditions<br />

for 14 d. A compatible interaction results in a<br />

change <strong>of</strong> the colony morphology along the entire<br />

agar strip. It may be expressed as appressed or<br />

crustose secondary mycelium. In a common B<br />

interaction. such changes occur only in the<br />

interaction zone. The ends <strong>of</strong> the agar strip remain<br />

white and fluffy while the midd'le section is<br />

appressed. Both the common A and common AB<br />

interactions remain fluffy and unchanged. The<br />

genotype <strong>of</strong> these can be deduced by studying the<br />

compatible and common B interactions. In addition,.<br />

by crossing with monosporous testers we found that<br />

nuclear migration occurs in common A and compatible<br />

interactions but does not occur in common B<br />

interactions.<br />

T.W. DARMONO and H.H. BURDSALL. JR. Center for<br />

Forest Mycology Research. Forest Products Laboratory.<br />

Gifford Pinchot Dr.. Madison. WI 53705. Evidence <strong>of</strong><br />

the dikaryotic cells <strong>of</strong> the stipe tissue <strong>of</strong><br />

Armillaria tabescens.<br />

Diploid nuclei are reported to occur not only in the<br />

basidia but also in the secondary mycelium as well as<br />

in the stipe tissue <strong>of</strong> Armillaria spp. In the study<br />

<strong>of</strong> the life cycle <strong>of</strong> Armillaria tabescens, we found<br />

that most viable single cells obtained by maceration<br />

<strong>of</strong> stipe tissue are capable <strong>of</strong> germinating to form<br />

clamp connections. Clamp connections are also<br />

present on hyphae developed from stipe tissue placed<br />

on malt extract agar medium for 2-3 d. Cultures <strong>of</strong><br />

single cell origin are capable <strong>of</strong> developing normal<br />

fruiting bodies. This evidence indicates that the<br />

dikaryotic phase is present in the stipe tissue <strong>of</strong> A.<br />

tabescens and leads us to believe that the general<br />

life cycle in Armillaria may not be as unusual as has<br />

been proposed.<br />

PX?Z E. DESJpP2Ih:S. Ncrthe-m Reqional Research<br />

Center, USDA/ARS, 1815 N. University Street, Peoria,<br />

IL 61604.<br />

Biochemical and Genetical Approaches to the Ecology<br />

<strong>of</strong> Phytopathogenic Fusarium<br />

Gibberella pulicaris (a~m3rph: Fusarium wrbucinum)<br />

is a heterothallic ascomycete and amenable to both<br />

classical and molecular genetic analyses. This<br />

species is broadly adapted as a soil saprophyte and<br />

as a plant pathogen with a wide host range. Our 5.<br />

pulicaris collection <strong>of</strong> more than 100 strains fran<br />

soils and from diseased plants presents a wide range<br />

<strong>of</strong> genetically inheritable variation for a ndxr <strong>of</strong><br />

traits that my be relevant to plant pathcqenesis.<br />

Many <strong>of</strong> these ecologically and geographically<br />

diverse, but morphologically similar, strains have<br />

mintdined their sexual interfertility, which allows<br />

confirmatior, <strong>of</strong> their identity as rmkers <strong>of</strong> a<br />

reproductively unique, biological species. Genetic<br />

anc3 biochemical analyses have identified tricho-<br />

thecene toxins and phytoalexin detoxification<br />

enzymes as important for pathogenicity <strong>of</strong> this<br />

species. Population analysis supports the hypothesis<br />

that selection for the ability to produce toxins<br />

and to aetor-ify phytoalexins has directed evolution<br />

<strong>of</strong> 5. pulicaris from a soil saprophyte to a plant<br />

pathogen.<br />

PHILLION and R. C. ANDERSON. Department <strong>of</strong><br />

Biological Sciences, Illinois State University,<br />

Normal, IL 61761.<br />

Mycorrhizal association <strong>of</strong> little bluestem on burned<br />

and unburned sand prairies.<br />

This study examined the influence <strong>of</strong> burning on the<br />

productivity, tissue inorganic nutrient<br />

concentration and vesicular-arbuscular mycorrhizae<br />

(VAM) fungus association <strong>of</strong> a sand prairie community<br />

in central Illinois. Burning significantly affected<br />

VAM fungus colonization and colonized root length,<br />

plant production and tissue inorganic nutrient<br />

concentration. Productivity was found to be.<br />

significantly higher on the- burned site than on the<br />

unburned during the growing season. For samples<br />

taken from May through October, percent Vm fungal<br />

colonization levels were significantly lower on the<br />

burned site than on the unburned site. In contrast,<br />

zolonized root lengths were longer on the burned<br />

site than on the unburned site but differences<br />

between sites were not always statistically<br />

significant. Above- and belowground tissue samples<br />

showed significantly higher levels <strong>of</strong> several<br />

inorganic nutrients on the burned site than the<br />

unburned site in early May and late June samples.<br />

This was true when nutrients were expressed as<br />

concentratiops($ and ppmi in tissue and nutrients in<br />

tissu~ per mL(mg and g/mL) .


STEPHAhTIE m, Department <strong>of</strong> Plant Pathology,<br />

University <strong>of</strong> Arkansas, Fayetteville, AR 72701 and<br />

KENNFM WELLS, Department <strong>of</strong> Botany, University <strong>of</strong><br />

California ,' Davis, CA 95616.<br />

Ustilago cvnodontis intersterility groups.<br />

The consistent nature <strong>of</strong> the pairing pattern <strong>of</strong><br />

single basidiospore isolates <strong>of</strong> Ustilago cvnodontis<br />

is confirmed. Infections <strong>of</strong> the host, Cynodon<br />

dactvlon from intra-and intercollection pairings,<br />

result in viable basidiospores. F, isolates <strong>of</strong><br />

field collecLions and selected laboratory pairings<br />

were examined for evidence <strong>of</strong> an intersterility<br />

system epistatic to the compatibility system. The<br />

nature <strong>of</strong> the partial intersterility isolates is<br />

stable. Germination rates <strong>of</strong> F progeny from<br />

Sntracollection pairings were reduced 1 in comparison<br />

with intercollection pairings. Intercollection<br />

experiments showed variability. Pooled data showed<br />

significant differences. Growth and infection was<br />

variable, when using the same isolates on different<br />

plants, pointing to the importance <strong>of</strong> the host in<br />

the developnt <strong>of</strong> Ustilago cynodontis.<br />

J, C. OW and D. J. Mclaughlin. Dept. <strong>of</strong> Plant<br />

Biology, Univ. <strong>of</strong> Minnesota, St. Paul, MN 55108.<br />

Cytology and phylogeny <strong>of</strong> the basidiomycete<br />

XenoaloeaerioDhori.<br />

Xeno- erioDhori (Auriculariaceae sensu lato)<br />

is a heterobasidiomycete parasitic upon sedge<br />

species. It has been collected in Minnesota from<br />

Scl rDuovirem. In an effort to clarify its<br />

relationships to other auriculariaceous fungi,<br />

Xenoaloea was examined ultrastructurally and<br />

ligh: microscopically. Meiosis begins and<br />

synaptonemal complexes are formed in<br />

probasidia which are produced within the leaf<br />

clustered beneath the stomata. Metaphase I is<br />

recognized in the metabasidia which emerge<br />

through and mature outside the stomata.<br />

Basidiospores are formed which may develop<br />

ballistospores or bud as yeasts. Ultrastructural<br />

characters <strong>of</strong> nuclear division and septa1 pore<br />

structure are believed to hold particular promise<br />

in establishing a phylogeny <strong>of</strong> auricularoid fungi.<br />

Xemghzi possesses a spindle pole body (SPB)<br />

with layered discs which nucleate a well-<br />

developed array <strong>of</strong> astral microtubules from<br />

metaphase to telophase. The SPB differs<br />

structurally between meiosis I and II. The hyphal<br />

septa are perforated by multiple simple pores.<br />

J.T.~ELL~EI~, D.A. GLAWE~, M.R. TAYSEY~, and L.L.<br />

TEWS . ,Dept. Biol. Sci., Univ. Tex., El Paso, TX<br />

79968. 'Dept. Plant Path., Univ. Ill., Urbana. IL<br />

61801, : ~ ~ ~ Biol., t . Ind. Univ., Bloomington, IN<br />

47405, Biol. Dept., Wisc. St. Univ., Oshkosh, WI<br />

54911. Mycology test bank (exam file): preliminary<br />

version.<br />

The MSA Teaching Committee, with permission from the<br />

MSA Council, has compiled and edited a collection <strong>of</strong><br />

mycology examination questions, for use by MSA<br />

members. The purpose <strong>of</strong> this test bank is to save<br />

teachers time and to improve the quality <strong>of</strong> questions<br />

available, not to provide a standardsfor assessment<br />

purposes or to suggest what should or should not be<br />

included in a curriculum. A progress report is being<br />

made at this annual meeting in order to solicit<br />

suggestions for the preliminary version <strong>of</strong> the test<br />

bank that is available for distribution. A final<br />

version will be available at the 1991 annual meeting.<br />

D. F. FAIIR. -tic Bobny and Myoology<br />

IaboliitOry, ARS, m, ElARC-WeSt, Beltsville, MD<br />

20705<br />

The species <strong>of</strong> -ria on<br />

The increasw in-t in the a~thraahOS2 <strong>of</strong><br />

cornus caused by Discula sp. bas stindated the<br />

study <strong>of</strong> other frPIJi that are found on dogwoods.<br />

Eleven taw <strong>of</strong> Sevtoria have been described on<br />

Cornus. The signific~ce <strong>of</strong> bosts, spore<br />

mrphology and mnidiogenesis in the del~neation<br />

<strong>of</strong> these Sevtoria species will be discussed.<br />

T. Flynn'. O.K. Miller, J:.', and H.H. Burdsal12. Dept. <strong>of</strong><br />

Biology, VPIBrSU, Blacksburg, Va 24060'. FPL, CFMR, P.O.<br />

Box 5130, Madison, Wi 5370j2<br />

DNA hybridization studies on the Armillaria mellea species<br />

complex.<br />

The Armillaria mellea species complex is a cluster <strong>of</strong><br />

morphologically similar, but reproductively isolated biological<br />

species. The extreme morphological similarity might suggest<br />

high genetic similarity, and this hypothesis was tested by<br />

comparing the genomes <strong>of</strong>56 strains representing eight North<br />

<strong>America</strong>n biological species. The genomes were compared by<br />

hybridizing heterologous whole-cell DNA preparations and<br />

assaying the duplex molecules with S1 nuclease. The mating<br />

compatibility and DNA hybridization experiments compared<br />

intersterile tester strains, isolated and identified by Jim<br />

Anderson, with isolates taken from a broader geographic area<br />

which includes the states <strong>of</strong> Wa, Az, 11, and Va. The genomic<br />

similarity within a given biological species ranges from about<br />

80-99%, and the similarity among biological species in the A.<br />

mellea complex ranges from 40-70%. The exannulate species,<br />

A. rabescens, shares about 30% similarity with the rest <strong>of</strong> the<br />

genus. These data confirm that these biological species,<br />

identified by mating compatibility, are genetically distinct<br />

entities, but identifying new strains using macroscopic<br />

compatibility assays can sometimes be misleading. Our<br />

hybrization experiments have measured similarity, and have<br />

shown variation in genetic complexity (genome size). The<br />

genetic complexity, estimated by homologous DNA<br />

reassociation rates (Cot curves), generally agree with the<br />

hybridization data. Species concepts. speciation, and alloploidy<br />

are discussed with these results in mind.


K. FCSS and J. R. GARCIA, Biology Deparbwnt, Ball<br />

State University, Muncie, IN 47306<br />

Methylation <strong>of</strong> proteins and phospholipids during the<br />

differentiation <strong>of</strong> ME racernosus.<br />

Earlier studies with this dimorphic mold shaied that<br />

the specific activity <strong>of</strong> S-Adenosylmethionine (SAM)<br />

Synthetase, the enzyme responsible for the synthesis<br />

<strong>of</strong> SAM, increased during the aerobic germination <strong>of</strong><br />

sporangiospores. Those studies showed that the<br />

enzyme activity remained at dormant-spore level for<br />

approximately the first 90 minutes and increased<br />

significantly after the 3 hour point, a time when<br />

the spores are rounded and swelling. The present<br />

study was undertaken in order to try and determine<br />

the reason(s) for the increase in specific activity.<br />

Studies designed to look a t total protein methyla-<br />

tion, during spore gemination, shai an initial in-<br />

crease at a time when the spores are swelling and a<br />

subsequent decrease as the smllen spores begin to<br />

£om germ tubes. Fkspholipid. methylation also<br />

shms the same general pattern. An examination <strong>of</strong><br />

individual methylated proteins revealed approximately<br />

seven proteins that are inethylated during germination.<br />

These proteins appear to be more highly methylated<br />

at a time when the swollen spores begin to synthesize<br />

gem tubes. These preliminan? results suggest that<br />

the observed increase in the specific activity <strong>of</strong><br />

SAM Synthetase might provide additional SAM for<br />

the observed methylations.<br />

ANDREA GARGAS and JOHN W. TAYLOR Dept, <strong>of</strong><br />

F'lant Biology, University <strong>of</strong> California,<br />

Berkeley, CA 94720.<br />

Molecular evolution and phylogeny <strong>of</strong> lichenized<br />

and non-lichenized fungi based on PCR amplified<br />

18s rDNA sequences.<br />

This study focuses on the relationships<br />

between the ascomycetous orders Pezizales.<br />

Helotiales . Lecanorales and Caliciales . We have<br />

used the polymerase chain reaction to amplify<br />

specifically the fungal nuclear 18s rDNA from<br />

both licherized and non-lichenized fungi. Their<br />

18s genes amplified so far vary in size from 1.8<br />

kb to 3.2 kb, and their DNA sequences (from<br />

asymmetric amplifications) supply additional<br />

evidence for insertions in this region.<br />

Arrangements <strong>of</strong> orders within the<br />

Ascomycotina remain controversial, and DNA<br />

sequences <strong>of</strong> this conserved molecule may be used<br />

as the basis for a phylogeny which integrates<br />

both lichenized and non-lichenized fungi. In<br />

addition, these symbioses provide compact systems<br />

for studies on coevolution between the fungus and<br />

the alga.<br />

- R. 1. GESSNER and L. A. CASTLEBURY. Department <strong>of</strong><br />

Biological Sciences, Western Illinois University,<br />

Macomb, IL 61455. Batch culture studies with<br />

Dendryphiella.<br />

Dendryphiella salina and D. arenaria are<br />

common deuteromvcetes found in coastal marine<br />

habitats. kr studied the culture conditions<br />

necessary tci grow inoculum for future fermentation<br />

studies. both species grew well on all the agar<br />

media tested and D. arenaria exhibited significantly<br />

better growth on YpSs agar. In standing broth<br />

culture, both species also grew best on YpSs.<br />

Growth occurred between 5-35 C and the optimum<br />

temperature for dry weight production was at 25-30 C.<br />

Maximum growth was achieved after 7 days in 25 ml <strong>of</strong><br />

medium in standing 125 ml flasks. Growth was<br />

initially greater in shake flasks but by day 5 the .<br />

dry weights were not significantly greater than in<br />

standing cultures.<br />

L w. Department <strong>of</strong> Botany,<br />

Unlverslty <strong>of</strong> Tennessee, Knoxville, TN 37996-<br />

1100. Varlatlon <strong>of</strong> matlng systens In<br />

Harasmlu&.<br />

Sixteen apecles representing seven sectlons<br />

In tlPrasmln& vere establlshed in monokaryon<br />

cultures made from fresh materlal collected<br />

from the Great Smoky and Blue Rldqe<br />

nountalns. Self-crosses revealed varlatlons<br />

in matlng system type at the sectional level.<br />

Some sectlons vere predominantly tetrapolar<br />

lbifactorlal), vhlle other sectlona vere<br />

elther predomlnantly blpolar lunlfactorlal)<br />

or furnished lnconcluslve patterns. Results<br />

<strong>of</strong> Inter-collection matlnqs vlth n. rotula,<br />

P~rrhoce~halus, B. slccua, and n.<br />

pulcherrl~es are reported, lncludlng<br />

lntercontlnental matlnqs.<br />

L. F. GRAND, R. K. JONES, AND R. D. MILHOW, Plant<br />

Pathology Department, Box 7616, North Carolina State<br />

University, Raleigh, NC 27695-7616. Colletotrichum<br />

spp. isolated from strawberries in North Carolina.<br />

In fall 1988 and spring 1989 a severe outbreak <strong>of</strong><br />

anthracnose on strawber~y cultivar Chandler provided<br />

an opportunity to compre ane identify the three<br />

species <strong>of</strong> Colletotrichum reported m strawberry in<br />

North Carolina. Of the 280 isolates obtained, 83%<br />

were identified as C. acutatum ard 17% as _C<br />

qloeo-rioides. C. fraaariae, previously an<br />

important cause <strong>of</strong>-anthracnose in North Carolina, was<br />

not identified. C. acutatum was isolated from<br />

diseased fruit, cfowns, stolons, petioles, and leaves<br />

while s. gloeo-rioides was isolated cnly from<br />

diseased crowns. Abundant perithecia <strong>of</strong> Glomerella<br />

cingulata, the teleomorph <strong>of</strong> C. loeosporioides, were<br />

prcduce6 in culture by isolatz


C. GRUHN and S.K. BOYLE, Departments <strong>of</strong> Biology<br />

and Pathobiology, Virginia Polytechnic Institute<br />

and State,University, Blacksburg, VA 24061.<br />

Inhibition <strong>of</strong> polyamine synthesis in dermatophytes.<br />

The diamine, putrascine, and the polyamines,<br />

spermidine and spermine are aliphatic cations<br />

required for normal growth and development in all<br />

cells. In bacteria and plants, putre_scine synthesis<br />

utilizes either ornithine decarboxylase (ODC) or<br />

arginine decarboxylase (ADC); fungal and mammalian<br />

cells appear to lack ADC. The minimal inhibitory<br />

concentrations <strong>of</strong> difluromethylornithine (DF'MO) and<br />

mon<strong>of</strong>luromethyldehydroornithine (MFMO), inhibitors<br />

<strong>of</strong> ODC, and diflurornethylarginine (DM), an<br />

inhibitor <strong>of</strong> ADC, were determined for Trichophyton<br />

and Microsporum species. In general, Trichophyton<br />

species were more sensitive than Microsporum<br />

species; DFMA inhibits growth as effectively as<br />

DFMO but at a 10-fold lower concentration. Both<br />

ODC activity and polyamine accumulation were<br />

inhibited in either genera. ADC activity was not<br />

detectable in either genera; conversion <strong>of</strong> radio-<br />

labeled DFUA to DFMO was not detected in spite <strong>of</strong><br />

demonstrable arginase activity. The ultrastructure<br />

<strong>of</strong> inhibited cells revealed disrupted calcium<br />

metabolism, increased mitochondria and altered<br />

membrane systems. DFMO limits dermatophyte<br />

growth by inhibition <strong>of</strong> ODC and polyamine synthesis;<br />

in contrast, DFMA limits growth in as yet unspecified<br />

manner as ADC was undetectable. The usefulness <strong>of</strong><br />

inhibitors <strong>of</strong> poiyamine synthesis in studying<br />

fungal biology or treating fungal infections<br />

remains to be explored.<br />

-- R. GWTA, R. K. JAYASWAL and L. A. LUCHER.<br />

Department <strong>of</strong> Biological Sciences, Illinois State<br />

University. Normal, IL 61761. Effect <strong>of</strong> DNA<br />

topoisomerase 11-targeting antitumor drugs on<br />

Neurospora crassa DNA topoisomerase 11.<br />

The antitumor drugs m-AMSA, ellipticine, etoposide<br />

(VP16-213) and teniposide (VM26) act as potent<br />

clastogens in mammalian cells by inducing DNA<br />

topoisomerase IS-mediated DNA strand breaks.<br />

Previous studies (Gupta, R, 1990. Mutation Res. 240:<br />

47-58) showed that 3 <strong>of</strong> these compounds were nonmutagenic<br />

in heterokaryon 12 (H-12), a strain <strong>of</strong><br />

--<br />

N. crassa that mimics a diploid eukaryotic system<br />

and can detect multilocus deletions. To test<br />

whether this nomutagenicity could be due to druginsensitivity<br />

<strong>of</strong> E. crassa DNA topoisomerase 11,<br />

--<br />

in vitro studies were initiated. Using crude<br />

nuclear extracts from H-12 as a source <strong>of</strong> DNA<br />

topoisomerase 11, the effect <strong>of</strong> the drugs on the<br />

enzyme was determined by the bacteriophage P4 DNA<br />

unknotting assay (Liu. L. F., Davis, J. L. and<br />

Calendar, R., 1981, Nucleic Acids Res. 9:3979-3989).<br />

Preliminary studies indicate that the compounds<br />

inhibit the unknotting <strong>of</strong> P4 knotted DNA, suggesting<br />

that DNA topoisomerase I1 <strong>of</strong> N. crassa is similar<br />

to that <strong>of</strong> other eukaryotes with relation to drug-<br />

sensitivity.<br />

S C G PT. ' T. D. LEA!lTERS1, G. ELSAYED' and C.<br />

&&em Apgional Res. Ctr., has, USDA.<br />

Peoria, IL 61604 and Biol. Control Insects Res.<br />

Lab., ARS, USDA, Colunbia, MO 65205.<br />

Regulation <strong>of</strong> insect cuticle-degrading enzymes £ran<br />

the mycoinsecticide Metarrhizium anisopliae.<br />

Metarrhizium anisopliae is a promising mycoinsecticide<br />

for biocontrol <strong>of</strong> agricultural pests. Its host<br />

range includes both the Greater Wax Moth (Galleria<br />

mllonella) ard the Cabbage Imper (Trichoplusia<br />

-<br />

ni). We obtained five strains <strong>of</strong> M. anisopliae £ran<br />

the USDA-ARS Collection <strong>of</strong> Ehtomogenous Fungi<br />

Cultures. These strains were sel&ed fran-a wide<br />

geographical range. Strains were cultured on a<br />

basal salts medium containing glucose, gelatin or<br />

wified cuticle £ran either G. mellonella or T.<br />

-<br />

ni. Cuticle-grown cultures OT three str& s-kwe.3<br />

elevated lwels <strong>of</strong> proteases when canpared to<br />

glucose or gelatin-grown cultures. Scme proteases<br />

shdRd as nwch as 10,000-fold induction by cuticle.<br />

There was a 2- to 6101d increase in endochithase<br />

activity in cuticlegrown cultures wer glucose<br />

gram cultures <strong>of</strong> all strains; exochitinase remained<br />

unchanged. Hawever, exochitinase in gelatin-grown<br />

cultures sha& a 5- to 4C-fold increase over that<br />

on glucose-gram cultures. Strain-dependent<br />

regulation <strong>of</strong> lipase was observed. Thus, natural<br />

strain variability was significant in enzyme<br />

patterns, and no evidence <strong>of</strong> coordi~te regulation<br />

was found. A correlation between enzyme lwels and<br />

virulence parameters was !-,at apparent. Thus,<br />

enzymes may not be the scl? vjrulenoe determinants<br />

and alternative factors such as toxins from<br />

entomqenous fungi are presently being explored.<br />

F.A. HANEY, A.E. LIBERTA, and R.C. ANDERSON. Dept <strong>of</strong><br />

Biological Sciences, Illinois State University,<br />

Normal, 11. 61761<br />

Influence <strong>of</strong> light intensity on growth and<br />

mycorrhizal colonization <strong>of</strong> little bluestem grass.<br />

Nonmycorrhizal plants grown in sterile and sterile-<br />

plus filtrate soil and mycorrhizal plants grown in<br />

unsterilized soil were grown under three light<br />

conditions; full sun. 70% full sun. and 53% full sun.<br />

Nonmycorrhizal plants produced significantly more<br />

biomass and total root length than mycorrhizal<br />

plants. Lower light intensities decreased<br />

mycorrhizal colonization as well as concentrations<br />

<strong>of</strong> nutrients including magnesium, zink, boron, iron,<br />

copper, and aluminum. Manganese did not decrease<br />

with light intensity but decreased in mycorrhizal<br />

plants.<br />

T. C. HARRINGTON. Department <strong>of</strong> Plant Biology,<br />

University <strong>of</strong> New Hampshire, Durham. N H 03824.<br />

Isozyme variation in Ceraocystis coerulescens, C.<br />

virescens and C. lariciwla.<br />

Starch gel electrophoresis was utilized to determine<br />

electromorphs for seven enzymes in Cerafocvstis<br />

coerulescens (Munch) Bakshi ;::asmorph = Chalara ungeri<br />

Sacc.) and three morpholog:-~~~ly similar taxa. Seven<br />

conifer isolates from North A;.;..;ics and Europe had similar<br />

electromorphs; each electromorpk wa' founi on both


continents. Conidia and conidiophores <strong>of</strong> these seven<br />

isolates were also morphologically similar and appeared to<br />

fit into a single species, i.e., C. coerulescens. Thirteen<br />

isolates from hardwoods (eight from maple trees with<br />

sapstreak disease and five saprophytic isolates) had<br />

identical electromorphs for five <strong>of</strong> seven isozymes and<br />

differed substantially from the conifer isolates in isozvme<br />

electromorphs. he hardwood isolates had narrower conidia<br />

and phialides than the conifer isolates. In spite <strong>of</strong> the<br />

synonymy supported by some, the hardwood type should be<br />

recognized as a distinct species, i.e., C. virescens (Davids.)<br />

C. Moreau. Apparently. C. virescens is restricted to<br />

eastern North Americn, where it may be a saprophyte on<br />

various hardwoods or a pathogen <strong>of</strong> maple. Cerafocys~is<br />

coerulescens sensu slriclo is more widely distributed and<br />

causes blue stain <strong>of</strong> coniferous wood. Five isolates <strong>of</strong> C.<br />

laricicola Redfern & Minter from larch in Scotland and the<br />

conifer isolates <strong>of</strong> C. coerulescens had nearly identical<br />

isozyme electromorphs, but ascospores <strong>of</strong> the former were<br />

slightly stouter than those <strong>of</strong> the latter. In contrast, a<br />

North <strong>America</strong>n isolate from Douglas-fir. designated as C.<br />

coerulescens f. douglasii by Davidson, was morphologically<br />

similar to isolates <strong>of</strong> C. coerulescens but had distinct<br />

isozyme electromorphs.<br />

C.K. HAYES, X. JIN and G.E. HARMAN. New York State<br />

Agriculture Experiment Station, P .O. Box 0462 Geneva,<br />

NY 14456.<br />

Principles in the development <strong>of</strong> biological control<br />

systems against plant pathogenic fungi.<br />

Growers have routinely used chemical pesticides to<br />

restrict the growth <strong>of</strong> plant pathogenic fungi.<br />

However, the public perceives that some <strong>of</strong> these<br />

chemical pesticides may pose threats to the<br />

environment or to human health. An alternative would<br />

be to utilize natural antagonists to these plant<br />

pathogenic fungi as bi<strong>of</strong>ungicides. Three basic<br />

requirements need to be meet for the successful<br />

utilization <strong>of</strong> a bi<strong>of</strong>ungicide. The bioprotectant<br />

strain employed must be genetically superior, either<br />

as a consequence <strong>of</strong> strain selection or genetic<br />

manipulation. The delivery system should stimulate<br />

the growth <strong>of</strong> the bioprotectant and provide a<br />

competitive advantage to it relative to competitive<br />

micr<strong>of</strong>lora. The biomass must germinate quickly over a<br />

range <strong>of</strong> environmental conditions and posses good<br />

shelf life, as a consequence <strong>of</strong> appropriate<br />

fermentation conditions. Considerable strides have<br />

been accomplished in developing biological seed<br />

treatment systems utilizing the filamentous fungi,<br />

Trichoderma. This fungi not only protects seeds, but<br />

colonizes and may protect the entire subterranean<br />

portions <strong>of</strong> plants. Consequently, plant growth and<br />

yield may increase. We utilized protoplast fusion to<br />

produce superior strains, developed seed treatment<br />

sysrems that provided reliable results, and are<br />

developing fermentation systems that give rise to<br />

efficacious~propagules. Consequently, this biocontrol<br />

system is expected to be marketed by a major<br />

corporation soon. Techniques refined by this research<br />

could be performed on other plant pathogenic<br />

antagonists thus evolving a class <strong>of</strong> biocontrol agents<br />

each specific for a particular group <strong>of</strong> pathogens.<br />

D. E. HEMMES AND R. C. RUABOHO. Biologv Department,<br />

University <strong>of</strong> Hawaii at Hilo, Hilo, HI 96720.<br />

Ultrastructural localization <strong>of</strong> adhesive material<br />

secreted by zoospores <strong>of</strong> Phytophthora palmivora<br />

usina lectin-gold complexes.<br />

Zoospores <strong>of</strong> Phytophthora palmivora are attracted .<br />

to roots, stems, and leaves <strong>of</strong> seedlings <strong>of</strong> Carica<br />

papaya where they encyst on or near the epidermal<br />

layers. Concanavalin A-colloidal gold complexes<br />

specifically label fibrillar material secreted by<br />

the zoospores and clearly identify the extent <strong>of</strong><br />

the adhesive material. Encysted zoospores adhere<br />

directly to the cuticle on leaves and stems and<br />

then produce germ tubes which enter stomata and<br />

hydathodes to reach the interior <strong>of</strong> the plant.<br />

At the root surface, however, zoospores <strong>of</strong>ten<br />

encyst 20-50 micrometers from the epidermal surface.<br />

Cysts adhere to each other, but adhesive material<br />

rarely extends to the root surface. Germ tubes<br />

grow from this halo <strong>of</strong> encysted zoospores to the<br />

root where they directly penetrate epidermal cells.<br />

Ultrastructural aspects <strong>of</strong> the secretion <strong>of</strong><br />

adhesive material will be discussed.<br />

J. E. HENDRIX, Z. -Q. AN, J. B. GROVE, D. E.<br />

HERSHMAN, and G. T. HENSON. Departments <strong>of</strong><br />

Plant Pathology and Agronomy, University <strong>of</strong><br />

Kentucky, Lexington 40546.<br />

Soil fumigation effects on vertical<br />

distribution <strong>of</strong> endogonaceous mycorrhizal<br />

fungi associated with soybean.<br />

Mycorrhizal fungi in a Western Kentucky<br />

soybean field were determined by MPN<br />

bioassay before and after fumigation with<br />

67% methyl bromide-33% chloropicrin and<br />

before and after growing a crop <strong>of</strong> soybeans.<br />

Giuas~ora aiuantea, Glomus macrocamurn, P.<br />

fecundis~orum and G. maculosum were present<br />

primarily in the upper 15 cm <strong>of</strong> soil, with<br />

few propagules at 30-45 cm. Of the species<br />

found at 30-45 crn, G ~ u ~ s maruarita D o ~ ~ and<br />

Glomus intraradices predominated. Soil<br />

fumigation eliminated most propagules in the<br />

upper 15 cm <strong>of</strong> soil but had little effect in<br />

the 30-45 cm layer. After production <strong>of</strong> a<br />

crop <strong>of</strong> soybeans, the population <strong>of</strong> total<br />

propagules had recovered in fumigated soil<br />

to prefumigation numbers and was higher than<br />

the population in non-fumigated soil. G.<br />

maruarita and G. 5ntraradices were a higher<br />

proportion <strong>of</strong> the total community <strong>of</strong><br />

propagules at the end <strong>of</strong> the season and may<br />

have had an advantage for recolonization<br />

because <strong>of</strong> their dominance at depths below<br />

the zone <strong>of</strong> effective fumigation. However,<br />

species which were less common deeper in<br />

soil also recolonized the soil effectively.


G.W. Hesseltine. 5407 N. Isabell, Peoria, IL<br />

61614<br />

New food ,fermentations: ragi and related<br />

products.<br />

In the Orient there are several different<br />

classes <strong>of</strong> food fermentations. One class<br />

including ragi, bubod, murcha, Chinese yeast,<br />

and look-pang are based upon solid dry inoculum<br />

used to start a variety 03 beverages and<br />

food fermentations. They are mixed cultures<br />

containing bacteria, yeast and fungi. A<br />

study <strong>of</strong> 114 strains <strong>of</strong> Mucor from 45 <strong>of</strong><br />

these starters showed that they belong to<br />

Mucor circinelloides (82) and g. indicus (32)<br />

with 6 not identified. Identification was<br />

based, in part, upon sexual reactions with<br />

known tester strains. None <strong>of</strong> the 56 Mucor<br />

strains tested utilized starch. fifty-three<br />

isolates from the amylase starters from 7<br />

regions showed that picros~orus (B.<br />

chinensis) and B. orvzae were the species<br />

present, and all <strong>of</strong> them caused hydrolysis <strong>of</strong><br />

starch. A third group <strong>of</strong> RhiZoDuS strains<br />

(7) were intermediate between B. orvzae and<br />

- R. micros~orus. Fourteen strains <strong>of</strong> RhiZoDuS<br />

tested for growth under anaerobic conditions<br />

grew bud did not sporulate. The third mold<br />

present was Amvlomvces rouxii, found in 7<br />

countries; 70 strains were isolated: and<br />

these produced amylases. When various combinations<br />

<strong>of</strong> microorganisms, isolated from<br />

amylase starters, were tested as mixed-culture<br />

fermentations, the only combinations<br />

that produced a good lao-chao product were<br />

the combinations <strong>of</strong> Saccharomvces fibuliaera<br />

with Mucor circinelloides, M. indicus, Rhizo~us<br />

micros~orus and Amvlomvces rouxii.<br />

is more closely related to the Polyporaceae<br />

than to the Tricholocataceae. Morphological<br />

characters (dimitic hyphae and hyphal pegs)<br />

are consistent with this hypothesis. The<br />

results also suggest that neither Lentinus or<br />

the Polyporaceae is monophyletic.<br />

T.*,<br />

H. C. HOCH, and B. TERHUNE. '~ept. <strong>of</strong> Biology,<br />

Rhodes College, Memphis, TN 38112, and Dept. <strong>of</strong> Plant<br />

Pathology, N. Y. State Agric. Exp. Sta., Cornen Univ., Geneva NY<br />

14456. lmmunolocalization <strong>of</strong> Coiled Cytoplasmic Filaments in<br />

Uromyces appendiculatus uredospore germlings.<br />

Uredospore germlings <strong>of</strong> Uromyces appendiculatus were homo-<br />

genized with glass beads, and a microparticulate fraction was<br />

produced by differential ultracentrifugation. The material was<br />

further fractionated on a column <strong>of</strong> Sephacryl S-1000, and a<br />

peak containing mainly flexuous coiled filaments was obtained.<br />

Their diameter was about 13 nm, and their typical maximum<br />

length was 500 - 540 nm. These appear similar to the "WFR"<br />

class <strong>of</strong> "virus-like particle" described by McDonald and Heath<br />

(1978. Can. J. Bot. 56:963-975). The major polypeptide <strong>of</strong><br />

the filament fraction has a molecular weight <strong>of</strong> about 36 kD, as<br />

measured by SDS-PAGE, with weaker bands between 29 and 34<br />

kD. Monoclonal antibodies were produced that were shown by<br />

immunoblotting to recognize an antigen that co-migrates with a<br />

34 kD protein <strong>of</strong> the filament fraction. With indirect immuno-<br />

fluorescence microscopy, the antibody labels fusiform struc-<br />

tures distributed throughout the cytoplasm. With EM immuno-<br />

gold labeling, the antibody binds to bundles <strong>of</strong> cytoplasmic<br />

filaments most closely resembling structures previously identi-<br />

fied as "filamentous distalsomes" (Hoch and Staples. 1983.<br />

Mycologia 75:795-824).<br />

David S. Hibbett and Rytas Vilgalys.<br />

Department <strong>of</strong> Botany, Duke University,<br />

~ukham, NC 27706. -<br />

Taxonomic relationships <strong>of</strong> Lentinus to the W. E. HIhTZ, J. C. ROYER, M. HUBBES and P. A. HORGEN.<br />

Polyporaceae: evidence from restriction<br />

Center for Plant Biotechnology, University <strong>of</strong> Toronto.<br />

analysis <strong>of</strong> enzymatically amplified<br />

Transformation-mediated insemonal mutagenesis <strong>of</strong> the dimorphic<br />

DNA. pathogen Ophoswma ulmi.<br />

Evolutionary relationships <strong>of</strong> Jentinus Fr. to<br />

the Polyporaceae were elucidated using<br />

restriction analysis <strong>of</strong> ribosomal DNA (rDNA).<br />

Five species in Mntinus sensu Pegler, three<br />

species in the Polyporaceae and two species<br />

in the Tricholomataceae were examined. RDNA<br />

phenotypes were determined by restriction<br />

analysis <strong>of</strong> enzymatically amplified rDNA (PCR<br />

Fingerprinting). This method generates<br />

Restriction Fragment Length Polymorphism<br />

(RFLP) data without Southern hybridization or<br />

autoradiography. With five different four-<br />

base restriction enzymes, one hundred unique<br />

restriction fragments were resolved. Among<br />

the 16 individuals examined, there were<br />

twelve unique rDNA phenotypes. A similarity<br />

matrix based on presence or absence <strong>of</strong><br />

comigrating restriction fragments was<br />

analyzed by clustering (UPGMA) and distance<br />

algorithms (Fitch-Margoliash analysis).<br />

Results <strong>of</strong> all analyses were highly<br />

consistent and strongly suggest that Lentinus<br />

Rotoplasts <strong>of</strong> Ophiostoma ulmi, the causal agent <strong>of</strong> Dutch Elm<br />

disease, were aansfmed to hygromycin resistance using a DNA<br />

vector (vPS57) containing a promoter for i~openicillin N synthetase<br />

from ~enicillibn chryso@& fused to a bac'terial gene f&<br />

hygromycin phosphotransferase. The transformation efficiency<br />

was 5 X 103 transformants per ug DNA per 10' protoplasts. The<br />

transforming DNA was stably integrated (mitotically) in single or<br />

tandem copies at unique or several &spersed sites within the<br />

transformant genornes. There appeared to be no targetting <strong>of</strong><br />

specific integration sites within the genome for the transforming<br />

DNA. This provided a useful approach for generating mutations by<br />

the insemonal disruption <strong>of</strong> functional genes. The crippled genes<br />

were conveniently tagged by the transforming DNA and could be<br />

recovered from genomic libraries. We have generated a<br />

developmental mutant (U9) in which the dimorphic phenotype has<br />

been altered. Unlike the untransformed parental strain the U9<br />

mutant fails to switch from yeast-like growth to mycelial pwth when transferred to selective medium. The transforming DNA<br />

integrated at a single locus and we hypothesize that the<br />

transforming DNA interupted one <strong>of</strong> the genes or regulatory<br />

regions essential to phenotype transition. We are currently<br />

analysing the site <strong>of</strong> inteption.


MICHAEL T. HOLMES, EDUARDO M. VADELL AND JAMES C.<br />

CAVENDER. Department <strong>of</strong> Botany, Ohio University,<br />

Athens, Ohio 45701. Ecological Aspects <strong>of</strong><br />

Dictyostelids in Tropical Forest Soils<br />

Our study site was at Tikal, Guatemala which is<br />

located at 17.5' N. latitude. The preserve consists<br />

<strong>of</strong> approximately 355 square kilometers <strong>of</strong> Semi-<br />

Evergreen Rainforest on limestone soils with 2500 mm<br />

annual rainfall occuring mostly during the months <strong>of</strong><br />

June through January. Twenty-five species <strong>of</strong> cellu-<br />

'lar slime molds, including four undescribed species<br />

were Isol.ated from a relatively small area <strong>of</strong> the<br />

preserve, in and around the ancient city <strong>of</strong> Tikal.<br />

Tropical forest are <strong>of</strong> particular interest because <strong>of</strong><br />

species richness and diversity in many taxonomic<br />

groups. Soil habitats in the tropical forest also<br />

appear to harbor equivalent species richness and di-<br />

versity based on our studies <strong>of</strong> cellular slime molds.<br />

Four trips (August '89, December '88, '89 and March<br />

'90) were made in order to study seasonal variation.<br />

Three sites <strong>of</strong> different moisture conditions were<br />

chosen for similarity analysis. Ecological analyses<br />

Cere conducted using regression models and analysis<br />

<strong>of</strong> variance. Our study has focused on the explora-<br />

tion <strong>of</strong> species richness and diversity through both<br />

microdistribution and macrodistribution within the<br />

Tikal area. We have also investigated the correla-<br />

tion between cellular slime molds and the abundance<br />

<strong>of</strong> bacteria and fungi in the soil. Future regenera-<br />

tion <strong>of</strong> tropical forest may depend upon the inocula-<br />

tion <strong>of</strong> cellular slime molds along with other micro-<br />

organisms into the soil. Therefore, preservation <strong>of</strong><br />

isolated species using the lyophilization process<br />

described by Raper and Alexander (1945) was an impor-<br />

tant Dart <strong>of</strong>. th~~-studv.<br />

John S. Hopple, Jr. Department <strong>of</strong> Botany,<br />

Duke University, Durham, NC. 27706.<br />

Phylogenetic Relationships Within the Genus<br />

Co~rinus Based on Molecular and Morphological<br />

Evidence.<br />

Evolutionary relationships <strong>of</strong> select taxa<br />

within the genus m~rinus were investigated<br />

using molecular and morphological data.<br />

Co~rinus atramentarius, C. cinereus, C.<br />

cornatus, C. micaceus, C, patoui1lardii;and<br />

C. plicatilis were selected as taxa<br />

representing a wide spectrum <strong>of</strong> variation<br />

within the genus for which adequate material<br />

was available. DNA coding for the large<br />

ribosomal subunit and part <strong>of</strong> the ITS region<br />

was amplified using polymerase chain reaction<br />

(PCR). A restriction fragment map <strong>of</strong> the DNA<br />

was obtained through a combination <strong>of</strong><br />

Southern blotting and PCR mapping.<br />

Morphological studies <strong>of</strong> the taxa were<br />

carried out through character analyses <strong>of</strong><br />

traditionally significant taxonomic<br />

structures. Evolutionary relationships were<br />

determined using phenetic and parsimony<br />

techniques. Significance <strong>of</strong> morphological<br />

characters governing taxonomic<br />

classifications will be discussed.<br />

Preliminary evidence supports the<br />

classifications <strong>of</strong> Moser (1983) and Orton<br />

and Watling (1979) at the sectional level.<br />

Further evidence indicates that Co~rinus is<br />

not a monophyletic group, but rather is<br />

paraphyletic.<br />

W. E. Horner and S. R. Lehrer. Tulane Medical<br />

Center, 1700 Perdido St., New Orleans, LA 70112.<br />

Allergenic/antigenic cross reactivity among<br />

basidiqmycetes.<br />

Basidiospore extracts contain allergens capable <strong>of</strong><br />

binding IgE antibodies and eliciting bronchial al-<br />

lergic responses in sensitized asthmatics. Immuno-<br />

print (IP) characterization <strong>of</strong> crude extracts <strong>of</strong><br />

Calvatia cyathiformis (Cc) with sera from skin test<br />

and RAST positive subjects demonstrated 21 a1 lergen-<br />

ic bands. Gal c Bd9.3 (pl 9.3, 16 kD), was the most<br />

important allergen, based on the number <strong>of</strong> sera<br />

(l2/l9), reacting to it. IP inhibition showed that<br />

Cc, Coprinus quadrif idus, Psi locybe cubensis and<br />

Pleurotus ostreatus each contain a pi 9.3 allergen<br />

that cross-reacts with the other species. Spore<br />

extracts <strong>of</strong> Pisolithus tinctorius and Ganoderma<br />

meredithae did not contain a 9.3 allergen. @lc<br />

Bd9.3 was isolated and rabbit antiserum was raised<br />

against it. lmmunodiffusion analysis <strong>of</strong> this<br />

antiserum against crude Cc extract and Calf BD9.3<br />

produced single precipitin bands that fused. IP<br />

with this serum also indicated shared epitopes for<br />

the 9.3 antigen among these four species. These<br />

results demonstrate shared antigens among four<br />

families in two orders <strong>of</strong> basidimycetes. The<br />

presence <strong>of</strong> shared antigens among basidimycetes may<br />

facilitate screening for basidiomycete allergies and<br />

aid phyletic studies.<br />

J. S. HORTON and C. A. RAPER. Department <strong>of</strong><br />

Microbiology and Molecular Genetics, University <strong>of</strong><br />

Vermont, Burlington, VT 05405.<br />

Pulsed-field electrophoretic analysis <strong>of</strong> $chizo~hvllum<br />

commune chromosomes.<br />

Transverse alternating field electrophoresis (TAFE) was<br />

used to separate chromosome-sized DNAs <strong>of</strong> the<br />

Basidiomycete ~chiw~hvllum commune. Six bands were<br />

observed in TAFE separations. ranging in size from 6200<br />

to 1250 kb. Three bands appeared to be doublets, as<br />

judged by the intensity <strong>of</strong> their ethidium bromide<br />

staining, and by hybridization analysis using cloned<br />

probes. Polymorphisms in chromosome size were<br />

observed between different strains <strong>of</strong> S. Fommuns. The<br />

results <strong>of</strong> DNA hybridization experiments suggested that<br />

certain genes previously determined by genetic analysis<br />

to reside on different linkage groups may be present on<br />

the same chromosomal DNAs. The utility <strong>of</strong> pulsed-field<br />

electrophoresis and chromosome-specific probes as an aid<br />

in the isolation <strong>of</strong> genes will be discussed.<br />

P. A. HUMBER. USDA-ARS Plant, Soil & Nutrition Labora-<br />

tory, Tower Rd., Ithaca, NY 14853.<br />

Thermotolerance <strong>of</strong> Conidiobolus species.<br />

Species <strong>of</strong> Conidrobolus (Entomophthorales: Ancylistaceae) are<br />

primarily saprobes occurring in plant dewitus and soil; sweral<br />

species occur primarily as enromopathogens; a smaller number<br />

<strong>of</strong> (saprobic andlor entomopathogenic) species can cause my-<br />

coses <strong>of</strong> humans, equines, or other mammals. Vertebrate conidi-<br />

obolomvcoses are usually confined to the nasal passages and to<br />

adjacent superficial tissues, both <strong>of</strong> which are generally appreci-<br />

ably cooler than the core body temperature; these mycoses are<br />

only very rarely deep-seated or systemic.


In this study, growth and survival <strong>of</strong> 47 strains from 2 16 species<br />

<strong>of</strong> Conidiobolus from the USDA-ARS Collection <strong>of</strong> Entomopathogenic<br />

Fungi (ARSEF; Ithaca. NY) were surveyed during 8-day<br />

exposures to 35, 40, and 45°C. Entomopathogenic Conidiobolus<br />

spp. showed variable ability to survive at 35'C, and little or none<br />

to survive at 40'C. Several isolates (especially those isolated from<br />

vertebrate mycoses) survived or grew at 40'C; a strain <strong>of</strong> what<br />

appears to be an undescribed Conidiobolus sp. isolated from a<br />

dispersed (and apparently fatal) mycosis in a human grew at 45'C.<br />

This study suggests that the further study oE entomopathogenic<br />

Conidioboluc species (other than C. coromlus) for biocontrol is<br />

still a reasonable possibility. Stria care should be exercised, however,<br />

to limit direct human cxposurc to Conidiobolus species<br />

since some taxa can survive temperatures at which inoculations <strong>of</strong><br />

mammals (especially if immunologically compromised) mipht<br />

allow the establishment <strong>of</strong> potentially catastrophic mycoses.<br />

Temperature may not be a factor in the localization <strong>of</strong> most cases<br />

, ~ vertebrate f conidiobolomycosis to the nose and adjacent<br />

tissues.<br />

L.J.HUTCHISOK. Centre de Recherche en Riologie<br />

Forestisre, Facult6 de Foresterie et de GGodGsie,<br />

Universit6 Laval, Sainte Foy, QuGbec, Canada G1K 7P4.<br />

Tie taxonomic significance <strong>of</strong> enzymatic activity by<br />

ectomycorrhizal members <strong>of</strong> the Agaricales in vitro.<br />

Cultures <strong>of</strong> Agaricalean fungi showed characteristic<br />

differences in their ability to degrade cellulose,<br />

lignin, pectin, lipid, amylose, gelatin, casamino<br />

acids or urea. The patterns <strong>of</strong> degradation observed<br />

reflected taxonomic affinities. For example, lipase<br />

activity was primarily detected in species <strong>of</strong> Amanita<br />

while amylase activity was found mainly in species<br />

<strong>of</strong> Amanita and Cortinarius. Gelatin degradation was<br />

particularly prominent among species <strong>of</strong> Lactarius<br />

section Dapetes. Laccaria and Hebeloma strongly<br />

degraded both casamino acids and urea. The<br />

degradation <strong>of</strong> these compounds has potential for<br />

differentiating cultures <strong>of</strong> ectomycorrhizal<br />

Agaricales particularly on a generic level. The<br />

results are also discussed in relation to the<br />

ecology <strong>of</strong> these fungi.<br />

K. A. ~acobsl, J. D. MacDonaldl, and K. wells2.<br />

l~ept. <strong>of</strong> Plant Pathology, University <strong>of</strong> California,<br />

Davis 95616, and Z~ept. <strong>of</strong> Botany, University <strong>of</strong><br />

California, Davis 95616.<br />

Identification <strong>of</strong> Armillaria spp. in California.<br />

Despite the wide distribution <strong>of</strong> Armillaria spp. in<br />

California, definitive identification <strong>of</strong> the species<br />

in this state has not been made. Basidiocarps were<br />

collected from trees, stumps and surrounding ground<br />

cover in forested and nonforested sites throughout<br />

Northern California. A variety <strong>of</strong> coniferous and<br />

hardwood hosts from inland and coastal areas are<br />

represented. Monosporous cultures were paired with<br />

known haploid tester strains to identify biological<br />

species. Forty isolates have been collected and<br />

those tested thus far were compatible only with<br />

Armillaria mellea (Group VI) and each other. These<br />

crosses indicate there may be little diversity among<br />

California Armillaria species. Results from further<br />

crossings and the implications <strong>of</strong> these findin~s on<br />

distributior. patterns <strong>of</strong> this fungus will be<br />

preser.:~;.<br />

E. I. J-H i 0. K. HILLER. Departlent <strong>of</strong> Bioloq)', Birqinir<br />

Pol}Tecbnic Institute and State University, BlaOurq, BA 24061.<br />

Wysioloqical and norpboloqical Variation Between Populations <strong>of</strong><br />

&ill!& as Deterrined by lycorrhizal Experiments.<br />

m,<br />

Hyyrrhiral synthesis studies revealed that allopatric populations <strong>of</strong><br />

differ in bost specificity. Tissue cultures <strong>of</strong> SL<br />

aranulatus used were fro1 Hepal, (associated with Pallichiana),<br />

Korea (u densiflora) and the U.S. (m m). lycorrhizal<br />

effectiveness was used to measure bost specificity. Useful characters<br />

were defined as those uhich were stable vithin a population and<br />

neasured differences between uninoculated controls and mycorrhizal<br />

treatrents. Usefu! characters, as defined by these two tests were:<br />

shoot wet weiqht, total wet weiqht, percentaqe mycorrhizal short roots,<br />

shoot dry weiqht, total dry ueiqht and Bartiq net'penetration. These<br />

characters were subsequently used to measure variation in mycorrhizal<br />

effectiveness awnq the allopatric populations <strong>of</strong> S..<br />

Isolates associated vith &Q& uere lost effective with &&&<br />

and least effective with the other trees, whereas isolates frol E<br />

vallichiana and L densiflora showed variable effectiveness with all<br />

three trees. Pbenetic analyses used to determine hou similarly the<br />

isolates responded uith the hosts, confilled these results. We conclude<br />

that isolates associated with &Q& are mt specific for this<br />

bost, whereas isolates from tbe other two trees are not host specific.<br />

These results are discussed and hypotheses put fonrard to explain then.<br />

S.W. KAMII\'SKYI & I.B. HEATH. Depl. Biology, York<br />

University, 471)i: Keele SL. North Yo* Ontario, Canada. M3J 1P3<br />

lmmunocytochemistry <strong>of</strong> cytoskeletal proteins in -.<br />

The obmycete, Saorolepnla W, is a tip-growing organism with an<br />

apical cap <strong>of</strong> actin. The morphology <strong>of</strong> this cap is relatcd to hypha!<br />

gro~dh; it has been suggested to sewe, among other possible fundions,<br />

as a mechanical support for the newly-foming ~ lwall. i Actin in<br />

different patterns is found in older regions where it presumably has<br />

other functions. These changes are likely to be related to the colocalized<br />

adin-binding proteins (ABPs). To test this hypothesis il<br />

will be necessary to use immunocylochemtst~ (1C) with fixation and<br />

permeabilization protocols which preserve the delicate and easilydisrupted<br />

actin arrays in lifelike configurations, using hyphae which<br />

are known to be F n g at the time <strong>of</strong> fmtion.<br />

Techniques were developed to tether hyphae on cwerslips, and to<br />

prepare them for rhodamine phalloidin (RPh) staining and 1C. These<br />

hyphae grow normally in nutrient solution, and are well supported<br />

during staining. Harsh permeabilizations, such as cold acetone,<br />

depolymerlze F-actin in -. Instead, we partially<br />

protoplasted with Driselase which did not affect the RPh pattem.<br />

Tethered hyphal tips <strong>of</strong> Sapmkgu can show the previously<br />

reported formalin-fixed RPh-staining pattern <strong>of</strong> a fine hBrillar cap<br />

giving way to subapical cables and plaques but the pattem varies<br />

with the fiwtion. High or low concentrations <strong>of</strong> formal~n followed by<br />

RPh result in poor preservation <strong>of</strong> parts <strong>of</strong> the actin array; this<br />

variant stability may be related to the ABP distribution. Fixation<br />

with paraformaldehyde-glutaraldehyde shows diffuse RPh staining<br />

which 1s most similar to the reported RPh pattem in living hyphae.<br />

Preliminary studies with IC <strong>of</strong> cytoskeletal components have<br />

shown that the anti-adin pattem is simllar to that <strong>of</strong> RPh, using<br />

post-IC RPh staining as an internal control and comparing FITC-<br />

IC/RPh to RPh-stained preparations. This suggests that our 1Cpreparation<br />

procedures do not significantly alter Saoroleplrla actin<br />

conhgurations. 1C-localization <strong>of</strong> ABP distribution will be discussed.


KAY, ERIC and RYTAS VILGALYS. Botany Department,<br />

Duke University, Durham, NC 27706<br />

Somatic Incompatibility and Genetic Variation in<br />

pleurotus ostreatus from North Carolina<br />

motus is a heterothallic-tetrapolar<br />

Basidiomycete which reproduces sexually through wind-<br />

dispersed basidiospores. We analyzed the genetic<br />

structure <strong>of</strong> a population sample <strong>of</strong> P. ostreatus from a two<br />

hectare area in Durham, N.C. using somatic incompatibility<br />

and RFLPs. Samples from each <strong>of</strong> 55 dikatyons were<br />

paired in all possible combinations on agar to determine<br />

somatic incompatibility between genetically distinct<br />

individuals. Data from 1520 pairwise crosses show: 1) few<br />

compatible interactions in pairings <strong>of</strong> isolates from a single<br />

log; 2) compatible pairings only between adjacent isolates<br />

from the same log; 3) no compatible interactions in pairings<br />

<strong>of</strong> isolates from different logs. These results indicate that<br />

numerous individuals may colonize a log and that asexual<br />

propagation does not occur between logs. A plasmid<br />

library containing randomly-cloned DNA restriction<br />

fragments from P. ostreatus was used to screen the<br />

population for RFLPs. Preliminary data show both nuclear<br />

and mitochondria1 polymorphisms within the population.<br />

These observations are consistent with the pattern<br />

expected for a genetically heterogenous outcrossing<br />

population occupying spatially discrete resource units.<br />

H. W. KELLER and H. J. ARNOTT. Department <strong>of</strong> Biology,<br />

Box 19496, The University <strong>of</strong> Texas at Arlington, Arlington,<br />

TX 76019. Phvsarum pulcherrimum and Physarum roseum<br />

(Myxomycetes, Physarales, Physaraceae): Assessment and<br />

comparison <strong>of</strong> taxonomic characters using scanning electron<br />

microscopy.<br />

Monographers have suggested that these two colorful species<br />

<strong>of</strong> the genus Physarum should be united because <strong>of</strong> inconstant<br />

differences in taxonomic characters. Physarum pulcherrimum<br />

is characterized by dark maroon, reddish violet or purplish<br />

colored sporangia. Pigmented calcareous granules spherical in<br />

shape and 1-2 urn in diameter cover the outer peridial surface;<br />

the inner peridial surface highlighted by a metallic gold<br />

sheen. Surfaces <strong>of</strong> calcareous granules as viewed with SEM<br />

are distinctly roughened, not smooth, as in other species <strong>of</strong><br />

Myxomycetes, including P. roseum. These calcareous granules<br />

(CaC03) serve as a key taxonomic character that distinguishes<br />

these two species. SEM <strong>of</strong> stalk external surfaces and<br />

fractured faces show calcareous granules embedded<br />

throughout in P. pulcherrimum, differing from the<br />

longitudinally wrinkled stalks without calcareous granules in<br />

P. roseum. X-ray microanalysis <strong>of</strong> sporangial components in<br />

the two species revealed differences in the distribution <strong>of</strong><br />

calcium and manganese. Physarum roseum is characterized by<br />

bright scarlet red sporangia. Pigmented calcareous granules<br />

restricted to outer peridial surfaces and capillitial nodes have<br />

smooth surfaces similar to other species in the Physaraceae.<br />

Spore size and ornamentation are similar in both species.<br />

Differences in color, stalk morphology, surface markings <strong>of</strong><br />

calcareous granules, distribution <strong>of</strong> mineral elements, and<br />

other more variable taxonomic characters, collectively serve to<br />

distinguish these two species.<br />

R. W. KFRRIGAN, P. A. HORGEN. AND J. B. ANDERSON.<br />

Department <strong>of</strong> Botany, Erindale College, University <strong>of</strong><br />

Toronto, Mississauga, Ontario, CANADA L5L 1C6.<br />

Genetic diversity in the global population <strong>of</strong> Agaricus<br />

bisporus.<br />

Genetic analysis <strong>of</strong> approximately ninety uniquely derived<br />

isolates <strong>of</strong> A. bisporus and allied species, using isozyme<br />

and DNA RFLP markers, has produced data which are<br />

informative about relationships at several evolutionary<br />

levels. Among wild individuals, most genotypes are<br />

unique. It is also possible to recognize geographically<br />

dispersed families <strong>of</strong> individuals which are putatively<br />

descended, via secondary hornothallisrn, from a single<br />

progenitor, and to distinguish these from other lineages in<br />

which outcrossing has intervened. At the population level,<br />

North <strong>America</strong>n populations <strong>of</strong> A. bisporus harbor more<br />

genetic diversity than what is found in the best available<br />

sample <strong>of</strong> European germ plasm. Hypotheses on the<br />

origin <strong>of</strong> the disjunct amphi-Atlantic populations <strong>of</strong> A.<br />

bisporus are still under evaluation. At the species level,<br />

there app,-ar to be three distinct species in our sample <strong>of</strong><br />

the macromorphologically homogeneous section<br />

Hortenses. The two tetrasporic species may be A.<br />

subperonatus and A. subfloccosus. These three species<br />

appear to be genetically more similar to one another than<br />

any <strong>of</strong> them are to A. bitorquis. A. pattersonae is even<br />

more distantly related.<br />

T. ICEh'T KIM! R.R. EURGESS and J.W .KO?TING, ~~Tl~orest<br />

Products Labcratoq~, One Gifford Pinchot Dr., ??adison,<br />

1.11 53705. 2~iotechnologp Center, University <strong>of</strong><br />

Wisconsin, l.!adison, VI 53705.<br />

Biopulping: Status and Prospects.<br />

$iopulping is the treatment <strong>of</strong> wood chips with limin-<br />

!degrading fungi prior to pulping. The woo6 is<br />

s<strong>of</strong>tened by the fungal treatment, so that mechanical<br />

pulping requires considerably less energy anC the<br />

pulp gives much stronger paps? than untreatel<br />

;controls. In a comprehensive, industry-supported<br />

research effort, we are evaluating the feasibility<br />

pf such "bio-mechanical1' pulping. Our effort involves<br />

Seven closely coordinated research teams: ,fungus<br />

i(se1ecting species and strains, optimizing treatment),<br />

knzyne (identifying beneficiel and deleterious<br />

!enzymes), pulp and paper (making and testing pulp<br />

and paper), molecular genetics (engineering fungal<br />

strains), scale-up and engineering (optimizing solid<br />

substrate "fermentation"), economics (evaluating<br />

economic feasiSiIity), en8 information (monitoring<br />

scientific and other literature). Results from tine<br />

rirst 2.5-years <strong>of</strong> this 5-year program are very .<br />

promising. Tnis lecture will summarize progress.


K.K. Klein and T.J. Leonard, Department <strong>of</strong> Biological<br />

Sciences, Mankato State University. Mankato MN 56002<br />

and Department <strong>of</strong> Botany, University <strong>of</strong> Wisconsin,<br />

Madison WI 53706<br />

Genetic control <strong>of</strong> dikaryotic sectoring in<br />

Schizophvllun commune.<br />

KLICH. M. A.. A. R. LAX and J. M. BLAND. USDA.<br />

ARS. Southern Regional Research Center, P.O. Box<br />

19687. New Orleans. LA 70179.<br />

Inhibition <strong>of</strong> some mycotoxigenic fungi by Iturin A.<br />

a peptidolipid produced by Bacillus subtilis.<br />

The current concern about potential environmental<br />

Sectoring, a phenotype in which there are distinct<br />

damage by commercial fungicides has led to an<br />

outgrowths from dikaryotic colonies, is under the<br />

increasing demand for new control methods.<br />

control <strong>of</strong> at least three different genetic loci<br />

Bacillus subtilis produces peptidolipid compounds<br />

in the basidiomvcete Schizophvllum commune. \de<br />

<strong>of</strong> the iturin group which have been shown to have<br />

have isolated one homokarvotic strain, dm71, which<br />

antifungal properties, but not all fungal species<br />

produces the sectoring plle~~olypt. when mated with<br />

are sensitive co these compounde. In this study.<br />

wild type strains W80 and Pil. A cross <strong>of</strong> Pi1 and<br />

the activity <strong>of</strong> Iturin A, produced by B. subtilis<br />

H13 also produces a sectoring dikaryon, as does<br />

strain B-3, was tested. Paper disks impregnated<br />

a cross <strong>of</strong> W80 and H13. W80 does not produce a<br />

with various concentrations <strong>of</strong> Iturin A were placed<br />

sectoring dikaryon when mated to Pil. Progency<br />

on agar plates seeded with conidia <strong>of</strong> toxigenic<br />

@f a cross <strong>of</strong> dm71 with W80, display segregation<br />

species <strong>of</strong> Fusarium, Penicillium or Aspergillus.<br />

for the sectoring phenotype when mated individually<br />

All isolates vere inhibited at Iturin A<br />

with wild-type strains H13 and Pil. 48 <strong>of</strong> 101 pro-<br />

concentrations as low as 4 ugldisk. Penicillium<br />

duced the sectoring phenotype when mated with H13<br />

italicum, P. viridicatum and A. ochraceus were most<br />

(approx. 1:l) and 73 <strong>of</strong> 101 produced sectoring when<br />

strongly inhibited by the iturin whereas P.<br />

mated with Pi1 (approx. 3:l). We conclude that<br />

citrinum, A. flavus, A. parasiticus, and F.<br />

there are two loci which determine sectoring in<br />

moniliforme were least sensitive to Iturin A.<br />

matings with Pi1 and one locus which determines<br />

sectoring in matings with H13. Statistical tests<br />

show that the sectoring determinant in the H13derived<br />

dikaryons is independent (not linked) to<br />

either <strong>of</strong> the two determinants in the Pil-derived<br />

ROBERT KOEHN and MELANI OAKLEY. Southwest Texas<br />

dikaryons. Progeny <strong>of</strong> a cross <strong>of</strong> Pi1 and H13 were<br />

State University, Department <strong>of</strong> Biology, San Marcos,<br />

tested for their ability to form sectoring dikaryons<br />

Texas. 78666<br />

with dm71 and W80. Results <strong>of</strong> this cross suggest<br />

that genes in both partners in a dikaryon are impor-<br />

A stinkhorn-grass symbiosis.<br />

tant for the sectoring phenotype.<br />

The lavender-hued "eggs" <strong>of</strong> Phallus hadriani (Vent.)<br />

were collected from a St. Augustine grass environment<br />

in November 1989. It was noted that the mycelial<br />

cord was attached to the grass roots. More careful<br />

observations indicated that the mycelial-grass root<br />

-<br />

association was ectomycorrhizal . We be1 ieve that<br />

I(-D- m I G 1 E.B. SlNUX and K.F. RAFFA.<br />

this association is <strong>of</strong> interest because grasses have<br />

w=-ml= <strong>of</strong> Plant Pathology ard EnmDlogy,<br />

not previously been known to form ectomycorrhizal<br />

-1 Labs, 1630 Lirden Drive, Madison, WI 53706. structures. Futhermore, stinkhorns have previously<br />

mistatic activity <strong>of</strong> extracts from red pine<br />

not been reported to form symbiotic relationships <strong>of</strong><br />

lmJtarauhium texebrantis.<br />

the mycorrhizal type.<br />

Fungi in the genus Le-urn exhibit vary-<br />

&-, <strong>of</strong> virulence on thelr coniferaus hmts. We<br />

wished to &tenhe if fungistatic mapands are L.M. KOHN and J.B. ANDERSDN. Dept. <strong>of</strong> Botany,<br />

involved in the defense <strong>of</strong> red p h to<br />

University <strong>of</strong> Toronto, Erindale College, Mississauga, Ontario,<br />

-rantis. Pentane &methanol SRracts werexmde Canada L5L 1C6.<br />

from the phloan <strong>of</strong> mature red pines subjected to the A dispersed, repetitive DNA element fingerprints mycelial<br />

foil* trea-: inoculation with viable L.<br />

compatibility groups in field samples <strong>of</strong> Sclerotinia<br />

terebmntis, inaxlation with autoclaved &.<br />

sclerotiorum.<br />

erebrant'<br />

Sixty-four sclerotial strains <strong>of</strong> Sclerotinia sclerotiorum were<br />

obtained from transects in two fields <strong>of</strong> Canola (oilseed rape)<br />

in Harriston. Ontario. Mycelial pairings <strong>of</strong> the strains in all<br />

chlor<strong>of</strong>orm, solubilized in amtone and water, and<br />

combinations on agar medium produced either a compatible<br />

reaction in which two strains merged to form one unitorm<br />

incorporated into potato dextrnse agar. Linear<br />

colony, or an incompatible reaction in which a reaction line<br />

graJth was significantly higher car uMmended media developed in the interaction zone and the two strains, though<br />

thanonmediaamm3edwithredpinee&actsan3.<br />

growing together, remained distinct. Among the 34 strains <strong>of</strong><br />

slightly, hut significantly, inhibited by extracts<br />

the first field. 6 mycelial compatibility groups (MCGs) were<br />

from ummuxled tissw. Extracts frm mchanically recognized, the largest group containing 17 strains. Among<br />

Klnrledaswellasinaxlatedtissue~<br />

the 30 strains <strong>of</strong> the second field, many more compatibility<br />

pronamced, significant inhibition <strong>of</strong> fungal grmth groups were defined. Three molecular criteria indicated<br />

w f i e n ~ t o e x t r a c t s f n r a ~ ~ luniformity s ~ within MCGs; by one <strong>of</strong> these criteria, each MCG<br />

uMmended media. These results indicate that the<br />

was uniquely fingerprinted. This fingerprint was produced by<br />

response <strong>of</strong> red pine to fungal invasion, as well as a random fragment <strong>of</strong> nuclear DNA (ca. 4.5 kb) from S.<br />

kcudiq, involves the prduction <strong>of</strong> some cmpmxI(s)<br />

capable <strong>of</strong> fungistatic activity.


sclerotiorum, pLK44.20, that when used as a cloned probe in<br />

Southern blots <strong>of</strong> DNAs restricted with m H l detected<br />

polymorphisms that corresponded exactly with strain<br />

groupings defined by mycelial compatibility. Another probe,<br />

plasmid pGP637, carrying the mitochondria1 24s rRNA gene<br />

from Neurospora crassa, in will digested DNA produced 3<br />

phenotypes that corresponded with groups <strong>of</strong> MCGs. The<br />

third molecular criterion used in this study compared DNA<br />

from each <strong>of</strong> the strains amplified by PCR with primer pairs<br />

defining a segment <strong>of</strong> the small mitochondrial rRNA gene,<br />

producing 2 phenotypes (fragment size <strong>of</strong> either 0.6 or 2.0<br />

kb) that corresponded with groups <strong>of</strong> MCGs. These data<br />

suggest that a held population <strong>of</strong> _S. sclerotlorum IS composed<br />

<strong>of</strong> aeneticallv dlst~nct "~ndlviduals". each ca~able <strong>of</strong> increaslna "<br />

by >sexual or homothalllc sexual reproduct;on.<br />

K.A.'. R.D. Kochn', Al. ~ohnson' and WJ. Rca'; 'Consultant,<br />

Dallas. Texas. $outhwest Texas Slate University. San Marcos, Texas<br />

78666. %viraunental Health Cenm - Dallas. 8345 Walnut Hill Lane<br />

#205. Dallas, Texas 75238.<br />

Preliminary obsavations on the airborne myc<strong>of</strong>loral component within<br />

the nonh Dallas memplex.<br />

Preliminary obsavations into the airborne myc<strong>of</strong>lora indigenous to the<br />

north Dallas region was conducted to obtain a better understanding as to<br />

the aer<strong>of</strong>ungal element <strong>of</strong> this area The primary goal <strong>of</strong> this initial<br />

investigation was IO conduct continual 24 how sampling for airborne<br />

fungal organisms to determine composition, frequency and seasonal<br />

periodicity <strong>of</strong> genera within the sampling region. Am sampling was<br />

performed using rotorod particulate sampling devices. Preliminary resul~s<br />

indicate a diverse fungal flora within the study region. with the occurrence<br />

<strong>of</strong> many genera strongly influenced by meteorological events. The<br />

tradillonal Deumomycetes were the most heavily represented, as<br />

expected. information resulung Erom am investigations are <strong>of</strong><br />

fundamental imponance in the clinical evaluation and ueaunent <strong>of</strong> the<br />

mold sensitive individual. Informarion resuldng from these initial studies<br />

inlcate a more exouc fungal flora which have not been traditionally used<br />

in the antigenic testing process. We believe these imtial studies are useful<br />

in the crearion. modification or elimination <strong>of</strong> panicular allergin mixtures<br />

used in the testingltreaunent process for patienu within this region<br />

B. T. LUI, J. A. GLASER~ and T. K. KIRK^. l~orest Producu<br />

Laboratory, lnstinrte for Microbial and Biochanical Technology, One Gifford<br />

Pinchot Dr., Madison, W1 53705. 2~.~. EPA. Risk Reduction Engineering<br />

Research Laboratory. 26 W. SL Clair Sr, Cincinnari. OH 45268.<br />

Use <strong>of</strong> white-rot basidiomycetes in the treatment <strong>of</strong> hazardous materials and<br />

hazardous wastes<br />

Research on the fungal bleaching <strong>of</strong> kraft pulp mill effluents led to<br />

investigations that demonsualed the ability <strong>of</strong> a 'while-rot' or 'lipindegrading'<br />

basidiomycete, Phancrochrc chrysosporium Burds.. to mineralize selected<br />

xenobiotics in liquid culture. Xenobiotics mineralized by ligninolytic culnues<br />

<strong>of</strong> this fungus include: DDT, lindane, 2,4.5-uichlwphenoxyacetic acid.<br />

several polycyclic aromatic hydrocarbons and various polychlorinated<br />

biphenyl. polychlorinated dioxin. polychlorinated aniline. and polychlorinaled<br />

phenol congeners. P. chrysosporium is also capable <strong>of</strong> effecting a rapid<br />

depletion <strong>of</strong> the wood preservative. pentachlorophenol, in soils into which it<br />

has been inoculated. The ability <strong>of</strong> this fungus to metabolize such a wide<br />

variety <strong>of</strong> xenobiotics has generated interest in using it and related fungi for<br />

remediation <strong>of</strong> contaminated soils. wastewaters and groundwaters. White-rot<br />

fungi are Nature's major degraders <strong>of</strong> lignin and a role for the Irgnindeprading<br />

system <strong>of</strong> these fungi in xenobioitc metabolism has been suggested bu~ not<br />

confumed. Evidence for this role includes the demonstrated oxidation <strong>of</strong><br />

selected xenobiotics by lignin peroxidases isolated from P. clqsosporium.<br />

The current status <strong>of</strong> research on xenobiotic metabolism by while-rot fungi<br />

will be described. Several remediation technologies that employ white-rot<br />

fungi exist in various stages <strong>of</strong> development. Examples are: (1)<br />

immobilization <strong>of</strong> fungal mycelia on various types <strong>of</strong> support materials<br />

through which aqueous media can be pgssed for ueaunent (e.g. The MyCoR<br />

Process which employs RBC technology) and (2) incorporation <strong>of</strong> solid<br />

substrates (e.g. wood chips). ha^ are infested with pure cultures <strong>of</strong> a selecled<br />

fungus, into contaminated soils for their remediation. Existing and potential<br />

'white-rot' remed~ation lechnolgies will be described and the latest f~ndings<br />

relaled.<br />

, S. C. GUPTA' , G. ELSAYED* ard C.<br />

-- ---. rthern Rwional Res. Ctr.. ARS. USDA,<br />

Peoria. i~ 61604 and 'Biol. Control ~Gects ~es.<br />

Lab., &, USDA, Columbia, MO 65205.<br />

Restriction Fragment Length Polymorphism as Genetic<br />

Markers for Beaweria bassiana.<br />

Natural isolates <strong>of</strong> the entcmog~ furigus<br />

Beaweria bassiana are abundant, and vary considerably<br />

in their virulence towards insect pests. The<br />

taxonaric significance <strong>of</strong> this strain variability is<br />

uncertain. B. bassiana is genetically inperfect,<br />

and mlecule techniques have not previously been<br />

applied to the taxonany <strong>of</strong> the species. Since lm<br />

virulence may be a limiting factor in the develop<br />

m t <strong>of</strong> entmcgenous fungi as mycoinsecticides, it<br />

would be desirable to exploit natural strain variability<br />

in the identification <strong>of</strong> high virulence<br />

isolates. Hawwer, direct assays <strong>of</strong> insect<br />

virylence are expensive, labor-intensive, and<br />

time-consuming. Consequently, restriction fragment<br />

length polymorphisms (RFLP's) were tested as genetic<br />

markers. Eleven strain <strong>of</strong> B. bassiana were chosen<br />

that exhibited a range <strong>of</strong> virulence against the<br />

Greater Wax Moth, Galleria rnellonella. A set <strong>of</strong><br />

random genaric DNk clones was isolated from representative<br />

strain NRRL 3108. These probes stringently<br />

hybridized to genanic blots frcm all strains,<br />

suggesting that these isolates are significantly<br />

related. Further, a n& <strong>of</strong> polymorphic<br />

differences were detected, sane <strong>of</strong> which appeared to<br />

correlate with virulence characteristics.<br />

S.B. Lee and J.W. Taylor. Department <strong>of</strong><br />

Plant Biology, University <strong>of</strong> California,<br />

Berkeley, California 94720 USA.<br />

Detection <strong>of</strong> species <strong>of</strong> Phvto~hthora by<br />

oligonucleotide hybridization.<br />

Differences among 5 species <strong>of</strong> phvto~hthora<br />

in the ribosomal DNA internal transcribed<br />

spacer (rDNA-ITS) were previously observed<br />

in sequence comparisons for phylogenetic<br />

analysis (see poster). Oligonucleotide probes<br />

for specific DNA sequences <strong>of</strong> phvto~ht hora<br />

cinnamomi, P. ~almivora, P. megvkarva, E<br />

c-, and Esitroohthora have been<br />

synthesized based on rDNA-ITS. Using<br />

primer directed enzymatic amplification <strong>of</strong>


specific genomic sequences (the Polymerase J. F. LESLIE, C. J. R. KLITTICH, and C. CHAISRISOOK.<br />

Chain Reaction or PCR) from nanogram Dept. <strong>of</strong> Piant Pathology. Throckmorton Hall, Kansas<br />

State University, Manhattan, Kansas 66506-5502.<br />

we were detect Fertility <strong>of</strong> isolates from Furarium section liseola.<br />

species specific nucleotide sequence variation<br />

by differential oligonucleotide hybridization Within Fusarium section Liseola four mating populations had<br />

in a sim~le dot-blot format. Due to the been previously recognized (A-D). We have crossed more than<br />

species siecific nature <strong>of</strong> these probes, this<br />

scheme may provide a simple, reliable<br />

scheme <strong>of</strong> species identification from small<br />

samples <strong>of</strong> infected plant tissues and can be<br />

applied to detection <strong>of</strong> obligate plant<br />

pathogens and mycorrhizal fungi.<br />

S.R. Lee and J.W. Taylor. Department <strong>of</strong><br />

Plant Biology , University <strong>of</strong> California,<br />

Berkeley, California 94720 USA.<br />

Molecular evolution and identification <strong>of</strong><br />

Phytophthora spp.<br />

Phgtophthora includes several species <strong>of</strong><br />

important plant pathogens. The high degree<br />

<strong>of</strong> morphological variability and the lack <strong>of</strong><br />

easily scored species characteristics has<br />

limited the number <strong>of</strong> phplogenetic studies in<br />

this genus. We are studying the molecular<br />

evolution <strong>of</strong> several species <strong>of</strong> Phytophthora.<br />

We have used the polymerase chain reaction<br />

(PCR) to amplify and directly sequence<br />

ribosomal DNA internal transcribed spacer<br />

regions (rDNA-ITS) <strong>of</strong> P hy t op h t h o r a<br />

cinnamomi, P. palmivora, P. megykarya, P.<br />

capsici, and P. citrophthora. This sequence<br />

data has been used to construct a phylogeny<br />

<strong>of</strong> these five species using DNA parsimony<br />

analysis. Results will provide an easily<br />

expandable data base for further phylogenetic<br />

analysis in the genus and related taxa. We<br />

have constructed species specific<br />

oligonucleotide probes to use in a simple,<br />

reliable scheme <strong>of</strong> species identification.<br />

T.J. LEONARD and T.J. VOLK.Departments <strong>of</strong> Genetics<br />

a d Botany, University <strong>of</strong> Wisconsin, Madison, WI<br />

53706.<br />

Production <strong>of</strong> new edible mushrooms in North <strong>America</strong>.<br />

Two relatively new edible mushrooms in the US market-<br />

place, Lentinula edodes (shiitake) and Morchella<br />

esculent2 (more1)will be discussed. Important<br />

physiological and ecological factors for spawn-run<br />

and mushroom production in shiitake, and key factors<br />

influencing sclerotium formation, germination and<br />

primordiurc formation in the morel will be emphasized.<br />

440 wild-collected isolates from the central and eastern United<br />

States with mating type testers representing these four popula-<br />

tions. Isolates belonging to the A. B and D populations have<br />

been identified and account for approximately 5046 <strong>of</strong> the iso-<br />

lates examined. Additionally, we have detected two more mating<br />

populations, E and l-, that account for a further 20% <strong>of</strong> the pop-<br />

ulation. Within the remaining 302 <strong>of</strong> the population there is<br />

preliminary evidence for three additional mating populations for<br />

which reliable testers are not yet available. Isolates from the A<br />

and F populations are all morphologically F. moniliforme; isolates<br />

from the B and E populations are all morphologically F. subglu-<br />

linans; and most isolates from the D population are morphologi-<br />

cally F. proliferarum.<br />

ESTELLE LEV-ET_;T.N, Faculty <strong>of</strong> Biological<br />

Science, The University <strong>of</strong> Tulsa, Tulsa,<br />

OK 74104<br />

The urban mushroom - an overlooked<br />

aeroallergen?<br />

Clinical investigations have shown that<br />

airborne basidioapores are significant<br />

allergens, however, very little<br />

information exists on the identification<br />

or concentration <strong>of</strong> these spores in the<br />

air. For the past three pears, the<br />

atmosphere in Tulsa has been monitored for<br />

the presence <strong>of</strong> basidiospores using<br />

Burkard Volumetric Spore Traps. The<br />

concentration <strong>of</strong> total basidiospores ahows<br />

that they are a significant component <strong>of</strong><br />

the Tulsa atmosphere during certain<br />

periods. During this study, spores from<br />

eighteen genera have been identified.<br />

Overall Coprinus spores are the most<br />

prominent genus represented; however<br />

Agaricus, Cal vatia, and Ganoderma spores<br />

are also abundant. Field studies in both<br />

wooded and urban areas indicate that<br />

fruiting bodies <strong>of</strong> all genera identified<br />

from the atmosphere are prevalent in<br />

lawns, parks, and fields within the city.<br />

This aerobiological data supports the<br />

clinical findings which show that<br />

basidiospores are an important group <strong>of</strong><br />

aeroallergens.<br />

JAMFS I FWIS and ROGER KOIDE. Dept. <strong>of</strong> Botany, Duke<br />

University, Durham. NC 27706 and Dept. <strong>of</strong> Biology, The<br />

Pennsylvania State University, University Park, PA 16802.<br />

Mycorrhizal infection increases <strong>of</strong>fspring vigor<br />

We studied the effects <strong>of</strong> myconhizal infection on <strong>of</strong>fspring<br />

vigor in Abutilon t h e m (velvetleaf). Maternal plants<br />

were grown in phosphorus-deficient autoclaved soil with<br />

low or high phosphate amendments or with Glomus<br />

etunicatum spores. Increased phosphorus availability and<br />

mycorrhizal infect~on significantly increased seed number


and seed phosphorus concentration, but did not<br />

significantly affect mean individual seed mass or seed<br />

nitrogen concentration. Seeds from each <strong>of</strong> five maternal<br />

plants from each maternal treatment were sown in soil with<br />

or without phosphate amendment. All plants were<br />

harvested after 35 days. Offspring from mycorrhizal<br />

mothers were significantly larger than <strong>of</strong>fspring from non-<br />

mycorrhizal mothers, regardless <strong>of</strong> maternal phosphate<br />

treatment. Maternal phosphorus treatment did not<br />

significantly affect <strong>of</strong>fspring vigor. Offspring phosphate<br />

treatment significantly affected <strong>of</strong>fspring growth but did not<br />

interact significantly with maternal treatment effects on<br />

<strong>of</strong>fspring vigor. Analysis <strong>of</strong> covariance suggested that the<br />

effect <strong>of</strong> myconhizal infection on <strong>of</strong>fspring vigor was due<br />

partly to changes in seed phosphorus content. This study<br />

showed that mycorrhizal infection <strong>of</strong> maternal plants can<br />

increase <strong>of</strong>fspring vigor.<br />

special problems, b'ecause (with very few exceptions)<br />

they are known to live only in the nonflying, aquatic<br />

larval stages <strong>of</strong> their mayfly, stonefly, or dipteran<br />

hosts. Six <strong>of</strong> the almost 100 known species <strong>of</strong><br />

Harpellales have broad host ranges and may be<br />

essentially cosmopolitan. However, the majority <strong>of</strong><br />

species appear to be geo aphically restricted and have<br />

narrower host ranges, % ndemic aquatic insect larvae<br />

in Australia and Kew Zealand contain some species <strong>of</strong><br />

gut fungi that are possibly autochthonous. Species <strong>of</strong><br />

Awtrosmittium in those countries may be vicariants.<br />

Costa Rican Harpellales are almost completely<br />

different from those <strong>of</strong> the United States at the species<br />

level. The hypothesis will be presented that the<br />

Harpellales began evolving with their hosts at a time<br />

when those insects were themselves evolving into<br />

extant species.<br />

A. E. LIBERTA, D. )I. WEST, C. S. CARLSON and J. N.<br />

ALBERT, Departments <strong>of</strong> Biological Sciences and<br />

Chemistry, Illinois State University, Normal. Ii<br />

61761. Antifungal activity <strong>of</strong> heterocyclic thio-<br />

J. LIFRAK, J. W. BENNETT, and J. DAVEY, Departments <strong>of</strong><br />

Biology and Eiectrical Engineering, Tulane University,<br />

New Orleans, LA 70118.<br />

semicarbazones and their metal ion complexes.<br />

The antifungal activity <strong>of</strong> a group <strong>of</strong> heterocyclic<br />

Effect <strong>of</strong> 60 Hz magnetic field on a duplication strain<br />

<strong>of</strong> Asperaillus nidulans.<br />

thiosemicarbazones and their metal ion complexes<br />

were assayed using five species <strong>of</strong> hyphomycetes<br />

that cause mild respiratory ailments in humans or<br />

are phytopathogenic. The five species differed in<br />

their sensitivity to the compounds that were<br />

assayed. The greatest inhibition <strong>of</strong> spore gencination<br />

in Asuereillus niRer occurred when its spores<br />

were treated wi n the copper (XI) complexes <strong>of</strong> 2-<br />

r;<br />

acecylpyridine K-diethyl-, 4K-dimethyi-, and 'Kdipropylthiosemicarbazone.<br />

Inhibition caused by<br />

these copper (11) complexes was up to 50Z greater<br />

:han that caused by Nystatin. The nickel (11)<br />

cornpiexes <strong>of</strong> the same thiosemicarbazones were<br />

substantially less effective in inhibiting spore<br />

germination. Paecilomyces variotii differed in its<br />

Epidemiological evidence implicating high power lines<br />

in the etiology <strong>of</strong> childhood cancer has stimulated interest<br />

in the development <strong>of</strong> a eukaryotic model for detecting<br />

chromosome rearrangements in the presence <strong>of</strong><br />

magnetic fields. A duplication strain <strong>of</strong> A- nidulans,<br />

carrying part <strong>of</strong> chromosome 1 attached to chromosome<br />

11, can be used to monitor chromosome breakage by the<br />

appearance <strong>of</strong> yellow spore Sectors among green ~010nies.<br />

Spore suspensions were exposed for 12 hours to<br />

a magnetic field generated by 30 ampere flowing in a<br />

dual Hemholtz coil exposure system generating 15<br />

gauss. Controls were incubated in an identical +emholtz<br />

apparatus without current or without coilc in a<br />

separate laboratory. Spore suspensions were plated<br />

On extract-glucose medium and incubated at<br />

response to these cosplexes in that nickel (11)<br />

complexes elicited an inhibitory response that was<br />

comparable to that caused by copper (XI) corcplexes.<br />

For P. variotii. Nystatin was less inhibitory than<br />

either the copper (11) or nickel (XI) complexes.<br />

These responses will be compared to those <strong>of</strong><br />

Aspergillus terreus, Botrvtis cinerea, and<br />

Penicillium rubrum. The pnysicai properties <strong>of</strong> the<br />

chemicals, as thev relate to their antifungal<br />

activity, will also be discussed.<br />

37 C. A minimum <strong>of</strong> 1000 colonies was couLted for<br />

each trial. lhe frequency <strong>of</strong> yellow sectors ranged<br />

from 1.6-1.82 for both controls and experimental cultures.<br />

Thus, no statistically significant difference<br />

between the rate <strong>of</strong> chromosome breakage in spore suspensions<br />

exposed or not exposed to magnetic fields<br />

was detected in this eukaryotic model system.<br />

W. W. LILLY. Dept. <strong>of</strong> Biology, Southeast Missouri<br />

State University, Cape Girardeau, MO 63701.<br />

Nitrogen source regulates mu1 tiple forms <strong>of</strong><br />

Proteases in Schizophyl luni commune.<br />

R. W. LICHTWARDT. Department <strong>of</strong> Botany, Proteolytic enzyme activity is derepressed upon<br />

University <strong>of</strong> Kansas, Lawrence, KS 66045. transfer <strong>of</strong> Schizophyllum commune homokaryons to<br />

Biogeography <strong>of</strong> trichomycete gut fungi and their nitrogen-deficient medium.=mitant with this<br />

arthropod hosts.<br />

derepression is alteration <strong>of</strong> the pattern <strong>of</strong><br />

protease electromorphs produced by the colonies.<br />

Since their evolution from free-living fungi, The source <strong>of</strong> nitrogen supplied in the growth<br />

Trichomycetes have become successfully established medium also affects changes in activity and<br />

throughout the world in insects, crustaceans, and protease forms. Colonies grown on equivalent molar<br />

milli edes. Present evidence, through far from concentrations <strong>of</strong> L-asparagine (the normal minimal<br />

com Pete, suggests that some species <strong>of</strong> Eccrinales and medi um nitrogen source), L-aspartate, L-glutamine<br />

~sefiariales in marine crustaceans may have dispersed<br />

and L-gl utamate show simi 1 ar patterns <strong>of</strong> protease<br />

with their hosts during the time the crustaceans were activity when separated on gelatin-containinc .<br />

radiating. The dispersal <strong>of</strong> the Harpeliales presents<br />

25


polyacrylamide gels. However, growth on other<br />

nitrogen sources produces distinctive patterns<br />

which are different from the minimal medium<br />

pattern. In some cases (eg. with arginine and<br />

cottonseed hydrolysate) this pattern is similar to<br />

the nitrogen-deficient colonies; in others the<br />

pattern is composed <strong>of</strong> selected electromorphs found<br />

in either minimal-grown or nitrogen-deficient<br />

colonies. The origin <strong>of</strong> the different protease<br />

forms is not clear. However, when extracts <strong>of</strong><br />

colonies grown on cottonseed hydrolysate are mixed<br />

with extracts <strong>of</strong> minimal-grown colonies, one <strong>of</strong> the<br />

major activities fro^ the minimal extract is<br />

destroyed. This suggests that some post-<br />

translational modifications may be involved.<br />

W.L LINGLE'. DJ. O'KANE~, and D. PORTER'. l~otan~<br />

Depanment and 2~iochemistry Depanment, University <strong>of</strong> Georgia,<br />

Athens, GA 30602<br />

Biolumln~cc Inheritance pattcms and sexual eompaUbillty In<br />

Pa& isolated from pine and hardwood.<br />

Panellus srvpticus is a white-rot basidiomycete <strong>of</strong> worldwide distribution<br />

found typically on hardwood substrates. The Nonh <strong>America</strong>n variety<br />

is bioluminescent but the nonhern European variety is not. Although<br />

75% <strong>of</strong> single spore isolates from basidiocarps on hardwood substrates<br />

were luminescent in culture. no single spore isolates obtained from<br />

luminescent basidiocarps on pine (an arypical substrate) were luminescent<br />

(as determined visually). Sexual compatibility and inheritance<br />

<strong>of</strong> luminescence were determined for six non-luminescent monobryons<br />

from pine crossed with themselves and crossed with 4 hardwood<br />

monokaryons characterized as either brightly luminescent, luminescent<br />

or non-luminescent. These crosses revealed that isolates from pine are<br />

the same biological species as isolates from hardwood and have a bifactorial<br />

mating system. Crosses <strong>of</strong> pine monokaryons with the<br />

brightly luminescent monoka~on always resulted in luminescent<br />

dikaryons, while those crossed with the luminescent monokaryon<br />

yielded a mixture <strong>of</strong> luminescent and non-luminescent dikawons, as<br />

did those with the non-luminescent monokaryons. Resula from<br />

crosses <strong>of</strong> pine isolates and hardwood isolates shw that inheritance <strong>of</strong><br />

luminescence is more complex than earlier results (Macrae, 1942) <strong>of</strong><br />

crosses between the non-luminescent European variet)' and the<br />

luminescent Nonh <strong>America</strong>n variety which indicated that luminescence<br />

was a dominant characteristic governed by one gene. Ainh and<br />

Foerster (1%) determined that at least 2 enzymes - NAD(P)H<br />

oxidase and luciferase - (and presumably 2 genes) were necessary for<br />

luminescence; perhaps explaining the complex pattern observed here.<br />

Complementation and/or additive effects <strong>of</strong> gene producu may occur.<br />

K.F. LOBUGLIO, S.O. ROGERS, and C.J.K. WANG.<br />

SUNY CESF, Syracuse, New York 13210.<br />

The Cenococcum geophilum - Elaphomyces Connection.<br />

The genus Elaphomyces (specifically species with<br />

blackish peridia) has been proposed to be the<br />

teleomorph, or sexual state, <strong>of</strong> C. geophilurr..<br />

Specimens <strong>of</strong> E. anthracinus were collected at the<br />

Huntington Wildlife Forest (SUNY CESF property) in<br />

the New York Adirondack mountains. Thirteen<br />

isolates <strong>of</strong> C. geophilum, representing three rDNA<br />

(ribosomal DNA) phenotypes, were collected at this<br />

same site two years prior to the Elaphomvces<br />

collection. An ertempt to verify the taxonomic<br />

connection between C. aeophilum an< Elaphomvces<br />

was carried out by comparing their tco RI rDNA<br />

pr<strong>of</strong>iles. The Eco R1 rDNA phenotypes <strong>of</strong><br />

-<br />

C. geophilurn isolates from the Adirondack site<br />

and other geographic locations, as well as DNA<br />

isolated directly from C. geophilum mycorrhizae<br />

adjacent to the Elaphomyces ascomata, did not<br />

correspond with the Eco RI rDNA pr<strong>of</strong>ile <strong>of</strong> the<br />

Elaphomvces collected.<br />

R. LOWEN & P. Diederich. The New York<br />

Botanical Garden, Bronx, NY 10458 &<br />

CUNY, 33 W. 42 St., New York, NY 10036;<br />

5 Rue Fernand-Mertens L-2148 Luxembourg.<br />

Two new lichenicolous spccies <strong>of</strong><br />

Pronectrja (Euascomycetes,<br />

Hypocreaceae) .<br />

A spccies <strong>of</strong> pronectria was discovered<br />

in the UK by Hawksworth on the lichen<br />

Xanthoria narietina. on a limestone wall.<br />

This was the only collection <strong>of</strong> the new<br />

taxon until Diederich collected the<br />

species in Luxembourg on )tanthoria<br />

parietina on a Po~ulus tree. Diederich<br />

also collected another new species on<br />

the lichen Thrombiun on soil in<br />

Luxembourg. These two new lichenicolous<br />

spccies <strong>of</strong> Pronectria will be described.<br />

Because immersed, light colored<br />

ascomycetes are so inconspicuous, many<br />

more undescribed species <strong>of</strong> Pronectria<br />

associated with their lichen hosts are<br />

likely to be discovered.<br />

MADOLE, GRETCHEN E, and JOHN C. C001iE. Department <strong>of</strong><br />

Ecology 8 Evolutionary Biology. University <strong>of</strong> Connecticut,<br />

Avery Pt., Groton, CT. 06340.<br />

A comparison <strong>of</strong> VAM infection on roots <strong>of</strong> Spartina patens<br />

and Distichlus spicata in a Connecticut coastal marsh.<br />

Studies <strong>of</strong> plants from freshwater and coastal marshes have<br />

shown that the development <strong>of</strong> mycorrhizal infection is<br />

affected by the underground water during the growing season.<br />

Increase. in root colonization by vesicular-arbuscular<br />

mycorrhizal (VAM) fungi has been noted as the water table is<br />

lowered. During a survey <strong>of</strong> coastal marsh plants, it was<br />

noted that Spartina patens and Distichlus spicata in high marsh<br />

areas <strong>of</strong>ten showed variation in VAM infection. Root samples<br />

from these two species were collected at several soil depths<br />

and compared for root infection. The samples were categorized<br />

as (1) lacking VAM fungi, (2) VAM fungi present but lacking<br />

vesicles &/or arbuscules or, (3) VAM fungi present with<br />

vesicles &/or arbuscules present. The results <strong>of</strong> this study<br />

will be presented.


MI and Y. Chen. Department <strong>of</strong> Biological Sciences.<br />

Brock University, St. Catharines. Ontario. L2S 3A1. Canada.<br />

Involvement <strong>of</strong> host cell surface agglutinin in attachment and<br />

appressorium formation by a mycoparasite.<br />

Cell wall proteins isolated from Mortierella pusilla and M.<br />

candelabrum. host and nonhost respectively to the<br />

mycoparasite. Ptptocephalis virginiana, were tested for their<br />

ability to agglutinate mycoparasite spores. SDS-Page revealed<br />

four bands (a, b, c, and d) <strong>of</strong> proteins present at the host<br />

surface, not at the nonhost surface, except for the faint band c.<br />

Deletion <strong>of</strong> proteins b or c from the host protein extract<br />

significantly reduced its agglutinating activity. Both proteins b<br />

and c were found to be glycoproteins and were required for<br />

agglutination. The results <strong>of</strong> agglutination and attachment tests<br />

obtained by various treatments <strong>of</strong> the host and nonhost cell wall<br />

proteins (including the two glycoproteins) and cell wall<br />

fragments showed: (1) the two glycoproteins are not only an<br />

agglutinin responsiMe for the mycoparasite spore agglutination,<br />

b; may also serve as a receptor for the specific recognition<br />

and attachment by the mycoparasite; (2) treatment <strong>of</strong> the<br />

mycoparasite spores with various sugars revealed that<br />

arabinose, glucose and N-acetylglucosamine inhibited the<br />

agglutination and attachment activity <strong>of</strong> the glycoproteins,<br />

however. the relative percentage <strong>of</strong> appressorlum formation<br />

was not sffected by the above sugars; (3) the two<br />

glycoproteins are relatively stable with respect to their<br />

agglutinin and receptor functions. The present results suggest<br />

that the agglutination and attachment may be mediated directly<br />

by certain sugars present at the host and mycoparasite cell<br />

surfaces while the appressorium formation may be the<br />

response <strong>of</strong> complementary combinations <strong>of</strong> both sugar and<br />

protein, the two parts <strong>of</strong> the glycoproteins at the interacl~ng<br />

surfaces <strong>of</strong> two fungi.<br />

D. H. Marx, S. B. Maul, and C. E. Cordell. Forest<br />

Service-USDA, Institute <strong>of</strong> Tree Root Biolo~y, Green<br />

Street, Athens, GA 30602; Mycorrtech, Inc., Univ. <strong>of</strong><br />

Pittsburgh Applied Research Center, 440 William Pitt<br />

Way, Pittsburg, PA 15238; and Forest Service-USDA,<br />

Forest Pest Management, Region 8, Asheville, NC<br />

28802, respectively.<br />

Application <strong>of</strong> specific ectomvcorrhizal fungi in<br />

world forestry.<br />

The dependence <strong>of</strong> many species <strong>of</strong> forest trees on<br />

ectomycorrhizae has long been recognized. Several<br />

methods have been used to ensure the development <strong>of</strong><br />

ectomycorrhizae on tree seedlings in nurseries for<br />

the establishement <strong>of</strong> manmade forests. Much work in<br />

recent years with a few fungal species has been<br />

aimed at selecting, propagating, manipulating, and<br />

managing the more desirable fungal species to improve<br />

tree survival and growth on a variety <strong>of</strong> regeneration<br />

sites. 'Much research has been done with the<br />

gasteromycete Pisolithus tinctorius throughout the<br />

world. Commercial vegetative and spore inocula <strong>of</strong> P.<br />

tinctorius are now in operational use in nurseries<br />

in the U.S. Spores <strong>of</strong> Rhizopogon vinicolor are also<br />

used in the Pacific Northwest in Douglas-fir<br />

container and bare-root nurseries. Vegetative<br />

inoculum <strong>of</strong> Laccaria laccata is being developed in<br />

Prance to inoculate Dougias-fir seedlings. Several<br />

research groups in Canada are examining the nursery<br />

and field significance <strong>of</strong> various fungi and methods<br />

ro produce vegetative inoculum. Research and develop-<br />

ment so far has only revealed a few <strong>of</strong> the potential<br />

uses <strong>of</strong> specific ectomycorrhizal fungi in world<br />

forestry. More basic and practical information must<br />

be revealed to fully utilize and inregrate the fungi<br />

into existing- forest -regeneration programs..<br />

I,.<br />

1<br />

H. Kothe', E- Kothe1, C-P- G. A. UARZLIIF. Departrent <strong>of</strong> Fiocheaistrp, The oh10<br />

k v o t n e c . ullrichl - ~ept. <strong>of</strong> ~otany' and State tfniversi ty, Colurhus. oP 4x10.<br />

~icrobiolog~~, University <strong>of</strong> Repulation <strong>of</strong> nitrocen aetabolisr in Neurospora.<br />

Burlington, Vermont 05405. Isolation <strong>of</strong> the<br />

mating-type locus from Schizo~hvllum t~mmune. Neurospora atiljlzes ~luta~ine, glutaaate, or amoniut.<br />

ions as its priraw nitropen sources anC will use<br />

An AA6 allele <strong>of</strong> the mating-type locus has these preferentiallv over secondary nitropen sources<br />

been isolated by screening an ordered cosmid vhicb include nitrate, purines, oeptldea and ranv<br />

library' <strong>of</strong> 5700 E.coli clones containing other co~pounds. The utilization <strong>of</strong> necondaq<br />

inserts <strong>of</strong> DNA from a Schizophyllum AA6 nitropen sources reowires the liftine <strong>of</strong> nitropen<br />

strain. The ordered library was divided into catabolic repression and saecific induction Bv<br />

120 subsets <strong>of</strong> 48 clones each. Cosmid DNA from suhrtrates or metahslic intereediates. The<br />

subsets was used to transform Schizophyllum structural penes which encodes nitropen catabolic<br />

trp- protoplasts to prototrophy by virtue <strong>of</strong> enzvmes are controlled Ev a well-defined net <strong>of</strong><br />

the Schizophyllum TRPl gene <strong>of</strong> the vector. repulatcp penes. Nit-2 is the malor oositive-<br />

Transformants were mated with a Schizophyllum act in^ control pene and is reouired for the exaressior,<br />

strain carrying & and AA alleles identical <strong>of</strong> all <strong>of</strong> the structural eenes within the nitropen<br />

to, but & and alleles different from, the circuit. Tbe nit-2 pene has beer! cloned and senuence<br />

transformation recipient. The recipient has and found to encode a repulatorq arotein <strong>of</strong> 1,036<br />

the same & but different AD as the donor DNA amino acids witb a sinple zinc finper elewnt whicb,<br />

used to make the library. Therefore, only trp' with an imediate downstrear. basic re~ion, functions<br />

transf ormants also transf omed by an allele as a seouence-speclfic DNA-bindinp dowain. Nitrate<br />

can undergo a positive mating reaction. A fnduction <strong>of</strong> the nitrate and nitrate reductase<br />

subset showing activity was subdivided and structural penes, e-? and z-6, respectlvelv, is<br />

the DNA tested by the assay described above mediated bv a oathrav-specific replulatoq pene. nit-4.<br />

until a single cosmid clone possessing &3<br />

activity was identified. The identity <strong>of</strong> the - Nit-4 is expres~ed constitutjvelv to vlelG a 2.5 kb<br />

transcriot which encodes a repjlatow protein with a<br />

- AR6 allele within this clone was demonstrated single completely distinct zinc ffnper dsain.<br />

since use <strong>of</strong> the allele to transform an A ExD~~SE~O~ cf the Lt-2 structural pene is hiphlv<br />

- 06 recipient did not activate A-regulated repulated at the level <strong>of</strong> ressearer RSA content. anC<br />

development. Subcloning <strong>of</strong> the AA6 allele and tbree hindinp sites for the oositive-actinf e-?<br />

a restriction map <strong>of</strong> the AD6 region will be nrotein are lccate6 in the 5' DTA unstreaa <strong>of</strong> s-3.<br />

presented.


G. May and P.3. Pukkila Dept. <strong>of</strong> Siology,<br />

University <strong>of</strong> North Carolina, Chapel Hill, NC<br />

27599-3280..<br />

Molecular cloning and functional analyses <strong>of</strong> the AJ<br />

mating type factor <strong>of</strong> Coprinus cinereus.<br />

We have isolated a cosmid clone with the entire 3<br />

mating type factor <strong>of</strong> Coprinus cinere-us.<br />

Subcloninc and transformatlon experiments reveal<br />

that: 1. both the 4 and the 6 subunits are present<br />

on this clone, 2. the d and' the 8 subunits are<br />

functionally redundant but not structurally similar<br />

and 3. that a cell activated for k controlled<br />

sequences is no longer able to accept nuclei in<br />

mating although it can donate nuclei to a strain<br />

.compatible at 8.<br />

We want to understand the evolutionary history <strong>of</strong><br />

different a1 leles. Genomic DNAs digested with<br />

various enzymes were blotted to nylon membranes and<br />

Southern hybridizations were made using large<br />

fragment o( and P (3.8 and 5.5 kb. respectively)<br />

probes as well as probes covering the regions<br />

between and outside <strong>of</strong> the subunits. These<br />

preliminary results indicate that rearrangements<br />

and length mutations are rampant and complex in the<br />

regions <strong>of</strong> & , b and in the DNA between the<br />

subunits while few such changes occur outside this<br />

area. Suprisingly, though o( and 6 are very<br />

tightly linked, we find very similar u and P<br />

alleles occurring independently <strong>of</strong> one another in<br />

isolates from different geographic locations (e.g.<br />

Japan and N.Carolina). Results will be compared to<br />

those obtaineG with mating type genes <strong>of</strong> other<br />

filamentous fungi.<br />

J.k. KcCAIN and C.J. MIROCHA. Dept. <strong>of</strong> Plant<br />

Pathology, Univ. o! Minnesota, St. Paul, 55108.<br />

Fungi isoiated from computer microdiskettes.<br />

Standard density 5 1/4-inch disk~ttes that<br />

ma1 functioned in the computer were examined for the<br />

cause <strong>of</strong> failure. Fungal hyphae were found on the<br />

surface <strong>of</strong> some diskettes obtained from colleagues in<br />

tropical countries. Fungi isolated on agar from the<br />

diskettes included species <strong>of</strong> Alternaria, As~erqillus,<br />

E~icoccum, Paecilomvces, Penicillium, and lrichoderma.<br />

Diskettes buried for three weeks outdoors in garden<br />

soil were colonized by species <strong>of</strong> Fusarium,<br />

Niqrosoora, and Trichoderma. These fungi and other<br />

species available in the laboratory were used to<br />

inoculate clean test samples, to approximate Koch's<br />

postul ates. Most species successfully colonized the<br />

diskettes within 3-4 days on agar at 25 or 32 C, 100%<br />

RH. Penicillium species dominated all others in mixed<br />

inoculations, although species <strong>of</strong> Chaetomium,<br />

Mvrothecium, Stachvbotrvs, and the other listed genera<br />

sporulated heavily in axenic culture on diskettes.<br />

Growth <strong>of</strong> all fungi was restricted to the 2-3 m thick<br />

surface emulsion <strong>of</strong> iron oxide with its organic<br />

dispersants and plasticizers, with hyphae not<br />

penetrating the mylar core <strong>of</strong> the diskettes.<br />

,B. A. MCDOK.4m. Department <strong>of</strong> Plant Pathology and<br />

Microbiology, Texas A&M University, College Station, TX<br />

77843-2132.<br />

DNA restriction fragment and chromosome polymorphisms<br />

in a Septoria trifiei population.<br />

Ten anonymous DNA probes were used to measure the amount<br />

and distribution <strong>of</strong> genetic variation in nuclear DNA among<br />

a sample <strong>of</strong> 93 Septoria tritici iteleomorph Mycosphaerella<br />

graminicola) isolates collected from a single wheat field.<br />

Nine <strong>of</strong> the probes detected restriction fragment length<br />

polymorphisms (RFLPs) at single-copy RFLP loci. The DNA<br />

fingerprint~ng probe pSTL40, which hybridized to 4-10<br />

hypervarioble RFLP loci, was used to assess clonal<br />

distribution and diversity. Identical clones were clustered in<br />

the field. All probes detected a high level <strong>of</strong> genetic variation<br />

distributed on a fine scale. Different pycnidia from the same<br />

lesion had different haplotypes in 45% <strong>of</strong> the comparisons.<br />

Genome rearrangements apparently occurred at a high<br />

frequency. Two <strong>of</strong> the single-copy probes detected deletions.<br />

Transverse alternating field electrophoresis showed that<br />

differences in chromosome size were common among the<br />

isolates. Data suggest that S. tritici populations possess a high<br />

level <strong>of</strong> genetic variability distributed in a fine-scaled mosaic<br />

on a microgeographical scale.<br />

D. J. McLwgMn. J. C. Doubl&s, and H. Lu. Dept. <strong>of</strong><br />

Plant Biology. University <strong>of</strong> Minnesota, St. Paul,<br />

MN 55108. Mitosis and the phylogeny <strong>of</strong> the<br />

basidiomycete Pachnocvbe ferrualnea.<br />

The gasteroid heterobasidiomycete eachnocvbe<br />

ferruainea produces holobasidia. Along with other<br />

simple-septate gasteroid taxa it has been<br />

classified in the Atractiellales, most <strong>of</strong> which<br />

form auriculariaceous basidia. Its affinities with<br />

these organisms and with ballistosporic species<br />

remains unclear. Ultrastructural analysis <strong>of</strong><br />

mitosis and the spindle pole body (SFB) provides<br />

clues to its relationships. Mitosis occurs in an<br />

acropetal wave in multinucleate apical cells <strong>of</strong><br />

the mycelium. The interphase SPB consists <strong>of</strong><br />

two connected discs. During metaphase the nuclei<br />

undergo a characteristic reorientation, the SPBs<br />

reside in a distinct polar fenestration in the<br />

otherwise intact nuclear envelope, and an ER cap<br />

encloses the pole. At telophase the SPB becomes<br />

displaced from the nucleus and a discrete bundle<br />

<strong>of</strong> astral microtubules develops. The significance<br />

<strong>of</strong> these findings will be discussed.<br />

MEREDITH. J. and R.C. ANDERSON. Biology Department.<br />

Illinois State University. Normal. IL 61761.<br />

The influence <strong>of</strong> varied microbial substrate<br />

conditions on the growth and mycorrhizal<br />

colonization <strong>of</strong> little bluestem (Schizachvrium<br />

sco~arium) .<br />

Plants were grown in three substrates (1) autoclaved<br />

soil, (2) autoclaved soil to which a VAM fungal-free<br />

filtrate <strong>of</strong> nonsterile soil was added and (3) non-<br />

sterile so:;. Preliminary studies revealed that


oot pieces treated with a 10% chlorox solution for<br />

at least 13 seconds, but not longer than 23 seconds<br />

could be used as aseptic VAM fungal inoculum in this<br />

study. To establish mycorrhizal plants in<br />

autoclaved soil, little bluestem root pieces were<br />

chlorox-treated for 9 to 17 seconds and used as a<br />

source <strong>of</strong> VAM fungal inoculum. Control plants were<br />

grown in substrates receiving autoclaved root<br />

pieces. Plants grown in the autoclaved soil had<br />

significantly (p


elationships among taxa at the species level<br />

and beyond. Techniques such as PCR enable<br />

the user to examine older herbarium specimens<br />

to determine relationships with living<br />

populations. Other studies examine groups <strong>of</strong><br />

taxa by classical morphological methods<br />

combined with genetic and molecular studies.<br />

Voucher specimens must be annotated in<br />

herbaria and so should vital information<br />

derived from the genetic an molecular<br />

studies. Many questions have arisen<br />

concerning the preservation <strong>of</strong> DNA and RNA,<br />

storage <strong>of</strong> such material, annotation <strong>of</strong><br />

studied material, use <strong>of</strong> old and new<br />

holotypes, etc. At present little<br />

information exists on the quantities <strong>of</strong><br />

material needed for various studies, the<br />

.preservation <strong>of</strong> copies or photos <strong>of</strong> gels, DNA<br />

"sequences and how to indicate exactly what<br />

material in a given collection was sampled.<br />

The round table discussion will attempt to<br />

examine the present and future problems and<br />

the issues which generate the greatest<br />

concerns for researchers and curators alike.<br />

The objective will be to draft a curatorial<br />

policy and uniform approach which can be<br />

presented to the MSA members and eventually<br />

implemented as policy by curators <strong>of</strong><br />

mycological collections for the greatest<br />

benefit to science.<br />

C. U. M1Mlr1, E. A. RICHARDSON' and J. KIMBROUGH~.<br />

l~e~artment <strong>of</strong> Plant Pathology. University <strong>of</strong> Georgia,<br />

Athens, GA 30602 and *Department <strong>of</strong> Plant Pathology,<br />

University <strong>of</strong> Florida, Gainesville. FL 32611.<br />

Ultrastructure <strong>of</strong> ascospore delimitation in freeze<br />

substituted samples <strong>of</strong> as codes mi^ hricans.<br />

Freeze substitution proved to be a useful technique<br />

for studying the early stages <strong>of</strong> ascosporogenesis in<br />

Ascodesnis niericang. Our observations indicate that<br />

the ascus vesicle originated from the ascus plasma<br />

membrane. Invaginations <strong>of</strong> the plasma membrane<br />

produced ascus vesicle initials consisting <strong>of</strong> two<br />

closely spaced unit membranes. The appearance <strong>of</strong> the<br />

outer leaflet <strong>of</strong> each <strong>of</strong> these membranes was identical<br />

to that <strong>of</strong> the inner leaflet <strong>of</strong> the ascus plasma<br />

membrane. Apparent points <strong>of</strong> continuity between ascus<br />

vesicle initials and the plasma membrane were<br />

observed. Ascus vesicle initials accumulated in the<br />

ascus cytoplasm near the plasma membrane and then<br />

coalesced to form the ascus vesicle, a peripheral,<br />

cylinder-like structure consisting <strong>of</strong> two closely<br />

spaced unit membranes that extended from the ascus<br />

apex KO the ascus base. The ascus vesicle then became<br />

invaginated in a number <strong>of</strong> regions and subsequently<br />

gave rise to eight sheet-like segments, or ascospore-<br />

delimiting membranes. that encircled uninucleate<br />

segments <strong>of</strong> cytoplasm forming ascospore initials.<br />

Like the ascus vesicle, each ascospore-delimiting<br />

membrane consisted <strong>of</strong> two closely spaced unit<br />

membranes, the inner <strong>of</strong> which became the ascospore<br />

plasma membrane. The ascospore wall developed between<br />

the spore plasma membrane and the outer membrane.<br />

Many details <strong>of</strong> ascospore maturation were clearly<br />

visible in freeze substituted samples.<br />

C. W. HlMS and K. M. SKETSELAAK. 1)epartment <strong>of</strong> Plant<br />

pathology, Univ. <strong>of</strong> Georgia. Athens, CA 30602.<br />

An ultrastructural study <strong>of</strong> teliospore maturation in<br />

the smut fungus Sporisoriwn sorghi using freeze<br />

substitution fixation.<br />

l'eliospores <strong>of</strong> the smut Sporisorium sorghi Lanpdon and<br />

Fullerton developed in galls produced in Sorghum<br />

Iralepense inflorescences. Small pieces <strong>of</strong> galls were<br />

freeze substituted and processed for study with TEM.<br />

This procedure yielded well-preserved spores in<br />

various staRes <strong>of</strong> maturation, and permitted detailed<br />

u?trastructural observations <strong>of</strong> stages difficult to<br />

preserve with conventional fixation pethods.<br />

Walls <strong>of</strong> sporogenous hyphae gelatinized, leaving<br />

uninucleate and apparently wall-less spore initials.<br />

Young teliospores then became surrounded by an<br />

electron.transparent primary wall. Electron dense,<br />

spine-like spore surface ornamentations developed<br />

adjacent to the plasma membrane and grew into the<br />

primary wall, which persisted as a sheath around the<br />

enlarging spines. A uniform layer <strong>of</strong> electron dense<br />

wall material was subsequently deposited beneath the<br />

spines. As spores matured, a less electron dense.<br />

fibrillar inner wall layer developed.<br />

Our interpretation <strong>of</strong> early stages <strong>of</strong> teliospore wall<br />

development is consistent with light microscope<br />

observations <strong>of</strong> S. sorghi and related species which<br />

describe gelatinization <strong>of</strong> sporogenous hyphal walls<br />

and development <strong>of</strong> spores frolo naked protoplasts. It<br />

differs from descriptions <strong>of</strong> taliosporogenesis in<br />

Tilletia species, where the primary spore wall does<br />

not arise de novo bur is continuous with the wall <strong>of</strong><br />

the sporogenous hypha.<br />

P. L. MINEHART and B. MAGASANIK. Department <strong>of</strong><br />

Biology, Hassachusetts Institute <strong>of</strong> Technology,<br />

Cambridge, MA 02139.<br />

Regulation <strong>of</strong> nitrogen assimilation.<br />

In 2. cerevisiae, at least two Independent systems<br />

exist which regulate the expression <strong>of</strong> genes involved<br />

in the assimilation <strong>of</strong> nitrogen. The first system,<br />

which responds to the intracellular glutamine to<br />

gltuamate ratio, regulates several genes including<br />

GLNl (glutamine synthetase), CDH2 (NAD-linked glutamate<br />

dehydrogenaae), and (general amino acid<br />

permease). In wild-type cells, the transcription <strong>of</strong><br />

these genes is repressed on glutamine and derepressed<br />

on glutamate. Two genes involved in this regulatory<br />

pathway. URE2 and E, have been defined. URE2 encodes<br />

a negative regulator which is believed to control<br />

the product <strong>of</strong> =, a positive regulator which<br />

contains a putative zinc finger DNA binding domain.<br />

Upstream analysis <strong>of</strong> various genes under the<br />

--<br />

URE2/GLN3 control has identified a consensus se-<br />

quence required for this control.<br />

The second system, which is less well defined,<br />

regulates protein levels in response to the presence<br />

or absence <strong>of</strong> a nitrogen source. The genes for<br />

amino acid permeases, including w, are subject to<br />

this regulation, which works at the transcriptional<br />

level. These permeases can be further subjected to<br />

post-transcriptional inactivation by either ammonia<br />

or glutamine.


E.A. MOMOL. J.W. KIMBROUGH, and H.C. KISTLER.<br />

Department <strong>of</strong> Plant Pathology. Universtty <strong>of</strong> Florida,<br />

Gainesville, FL 3261 1.<br />

Electrophoretic karyotypes are dissimilar for two strains <strong>of</strong><br />

Fusarium owsDorum that differ in host range.<br />

Protoplasts were obtained from strains <strong>of</strong> two formae<br />

speciales <strong>of</strong> the wilt pathogen Fusarium owsporum. To<br />

determine if genetic recombination could occur, protoplasts<br />

<strong>of</strong> strain ATCC 9990 E. owsporum 1. sp. conalutinans (a<br />

cabbage pathogen), and <strong>of</strong> strain ATCC 16601 E. owsporum<br />

f. sp. raphani (a radish pathogen) were fused in the presence<br />

<strong>of</strong> PEG. Chromosomes <strong>of</strong> fusants and parental strains were<br />

separated using contour clamped homogenous electrical field<br />

(CHEF) gel electrophoresis. . Karyotypes differed greatly<br />

between strains and minimum number <strong>of</strong> 11 and 8<br />

chromosomal bands were detected for ATCC 16601 and<br />

ATCC 9990 respectively. Saccharomvces cerevisiae and<br />

Schizosaccharomvces pombe chromosomes were used as<br />

molecular size markers. Although strain ATCC 16601 and<br />

strain ATCC 9990 had such different chromosome patterns,<br />

chromosomal banding pattern <strong>of</strong> fusants were identical to<br />

parental strains.<br />

J.THOMAS MULLINS. Department <strong>of</strong> Botany,<br />

University <strong>of</strong> Florida. Gainesville, FL<br />

32611. Structure and function <strong>of</strong> soluble<br />

cytoplasmic beta-glucans in Achlve.<br />

Water-soluble beta-glucans are major<br />

cytoplasmic constituents <strong>of</strong> Achlve. Two<br />

forms <strong>of</strong> these glucans were found, a<br />

neutral type (18%) and an acidic<br />

phosphorylated type (82%). Both forms<br />

release only glucose on hydrolysis, and<br />

the polymer is formed by beta-glucosidic<br />

linkages. These glucans function as<br />

carbon, and probably phosphorus, reserves<br />

in the mycelium, that support sexual and<br />

asexual reproductive cycles during<br />

staravation conditions. At least one<br />

beta-glucanase can be demonstrated in the<br />

mycelium, which is capable <strong>of</strong> hydrolyzing<br />

these glucans.<br />

MELANI K. OAKLEY. DAVID E. LEMKE and ROBEm D.<br />

KOEHN. Department <strong>of</strong> Biology. Southwest Texas State Uni-<br />

versity. San Marcos. TX 78666 -- Endomycorrhizal inoculum<br />

potential <strong>of</strong> surface mined lands: A bioassay <strong>of</strong> different aged<br />

sites.<br />

Mycorrhfzal inoculum potential IMIP) <strong>of</strong> a site has been<br />

recognized as an important factor in the reclamation <strong>of</strong> surface<br />

mined lands. Successful revegetation efforts may well<br />

hinge on the amount <strong>of</strong> V-A mycorrhizal inoculum present.<br />

After d~sturbance. an unknown penod <strong>of</strong> time must elapse<br />

before the MIP reacnes its pre-disturbance level. At a lignite<br />

mine m central Texas. spoils varying in age from 0-35 years<br />

were sampled, as was soil from an adjacent. undisturbed area<br />

<strong>of</strong> the mine. These samples were anaiyzed for nurrient availa-<br />

bility and pH. and bioassayed to determine the MIP for each<br />

site. The bioassay was conducted uslng corn seedlings grown<br />

in undiluted soil. as well as in soil dilutions <strong>of</strong> 1:4 and 1:40.<br />

and undiluted sterilized soil. Roots were harvested after<br />

periods <strong>of</strong> 30. 60. and 90 days and examined for the presence<br />

<strong>of</strong> V-A mycorrhizal fungi. The MIP <strong>of</strong> the undisturbed soil<br />

was greater than 50 percent, while that <strong>of</strong> the other sites de-<br />

clined in proportion to their ages.<br />

L. A. O'GORHAN, E. W. ROBINS. J. HAN, R. GUPTA and<br />

H. E. BROCKMAN. Department <strong>of</strong> Biological Sciences,<br />

Illinois State University, Normal, IL 61761.<br />

Viability <strong>of</strong> ad-3 mutant conidia <strong>of</strong> Neurospora<br />

crassa in pH 7 media.<br />

We use plates <strong>of</strong> Westergaard's basal medium<br />

supplemented with calcium pantothenate, casamino<br />

acids, a mixture <strong>of</strong> vitamins, a trace (0.1 uglml) <strong>of</strong><br />

adenine sulfate, and 1% sucrose (reversion medium)<br />

for assaying the reversion <strong>of</strong> ad-3 mutants <strong>of</strong><br />

Neurospora crassa carrying pan-2 and cot-l (causes<br />

colonial growth) markers. Plates <strong>of</strong> the same medium<br />

supplemented with 25 ug <strong>of</strong> adenine sulfate/ml<br />

(survival medium) are used for measuring conidial<br />

viability in the reversion experiments. We noted<br />

low conidial viability (~5%) when the survival<br />

medium was adjusted to pH 7, but not to pH 5 or 6.<br />

This low viability at pH 7 was not observed with<br />

another plating medium (Fries' basal medium<br />

supplemented with calcium pantothenate, 100 ug <strong>of</strong><br />

adenine sulfate/ml, and 0.52 each <strong>of</strong> fructose and<br />

glucose). Data will be presented showing that the low<br />

viability in the survival medium at pH 7 is not due<br />

to the difference in adenine sulfate concentration<br />

or the presence <strong>of</strong> casamino acids or the mixture <strong>of</strong><br />

vitamins, but is due to the presence <strong>of</strong> sucrose<br />

rather than fructose and glucose. When the standard<br />

2 X lo7 conidialplate from each <strong>of</strong> 2 ad-3 mutants<br />

were used on plates <strong>of</strong> the reversion medium, the<br />

spontaneous reversion frequency was about the same<br />

at pH 6, 7, and 8. We conclude that the decrease<br />

in viability <strong>of</strong> conidia from ad-3 mutants <strong>of</strong><br />

-- N. crassa in pH 7 media is dependent on carbon<br />

source and conidial concentration.<br />

W. J. OTROSINA. T. E. CHASE. F. W. COBB, JR.. and K.<br />

KORHONEN. USDA Forest Service. 1960 Addison Street,<br />

Berkeley. CA. 94701; University <strong>of</strong> California.<br />

Department <strong>of</strong> Plant Pathology. Berkeley. CA, 94704;<br />

and Finnish Forest Research Insititute. Helsinki.<br />

Finland.<br />

Allozyme comparisons between intersterility groups <strong>of</strong><br />

North <strong>America</strong>n and European Heterobasidion annosum.<br />

Allozyme analyses were conducted for S, and P<br />

intersterility (IS) groups <strong>of</strong> H. annosum from Europe<br />

and western North <strong>America</strong>. Eleven enzyme systems and<br />

13 loci were resolved. Very few alleles were shared<br />

between IS groups from western North <strong>America</strong>.<br />

indicating a large degree <strong>of</strong> genetic divergence and<br />

lack <strong>of</strong> gene flow between them. Several loci such as<br />

alcohol dehydrogenase, aconitase, and malate<br />

dehydrogenase were virtually fixed for alternative<br />

alleles between the two biological species and could


e used diagnostically to distinguish them. In<br />

contrast, the European populations <strong>of</strong> the S and P. IS<br />

groups are not as readily differentiated from each<br />

other, although there are considerable allele<br />

frequency differences between them. In general. the<br />

European S and P groups appear more related to the<br />

North <strong>America</strong>n S group than the North <strong>America</strong>n P<br />

group. Thus. the P group from North <strong>America</strong> and P<br />

group from Europe may have been derived from<br />

independent speciation events. These-data raise<br />

questions <strong>of</strong> how factors such as host selection, host<br />

species distribution, and paleoecological events have<br />

intpracted with reproductive isolating mechanisms to<br />

influence evolutionary divergence in H. annosum.<br />

M.E. Palm, USDA/APHIS/PPQ, Systematic Botany and<br />

Mycology Laboratory, BARC-West, Beltsville, MD<br />

20705.<br />

Pilidium concavum - synanamorph <strong>of</strong> Hainesia lythri.<br />

Single conidial isolates <strong>of</strong> Pilidium concavum (Desm.)<br />

Hohnel consistently yielded both sporodochia <strong>of</strong><br />

Hainesia lythri (Desm.) Hohnel and conidiomata <strong>of</strong><br />

- P. concavum. This confirms the observations <strong>of</strong><br />

Shear and Dodge (Mycologia 13:135-170. 1921) that<br />

the two are synanamorphs, with a Discohainesia<br />

oenotherae (Cooke & Ellis) Nannf. teleomorph (as<br />

Pezizella lpthri (Desm.! Shear & Dodge). Cultural<br />

characters on several agar media and conidiomatal<br />

morphology on alfalfa stems and blackberry twigs<br />

were recorded. Based on examination <strong>of</strong> type<br />

specimens, Sclerotiopsis testudinea Desm. is an<br />

additional synonym <strong>of</strong> P. concavum.<br />

;. G. PELYE?, 0. I(. 14iLLEE. JE., & C. GilUBIi.<br />

Departmen; <strong>of</strong> Biology, Virginia Polytechnic<br />

Inszi:~.te ad Etaze University, Elacksburg, VA. 24061.<br />

Ectoqvcorrilzal fungi frdizing on burned an? unburnel<br />

pine plots after e lcng &ought in the Virginie<br />

~ppalachians<br />

.<br />

A third successive dry year was predicted for 1988.<br />

liumerous lightening fires during 1957 suggested the<br />

need for litter- an8 shrub-free fire breaks on the<br />

Jefferson Iiational Forest. In February one control<br />

burn for this purpose split a stand <strong>of</strong> Pinus pungensl<br />

P. riside with scne oak into two plots <strong>of</strong>' equal area.<br />

--<br />

An unburned star.< <strong>of</strong> ?inus virgixiana with similar<br />

area but fewer ocr.s occupied a lower and more moist<br />

site. After a ho:, ary six weeks, :he first duffmoistenlng<br />

rain since nid-April fell on .July 13.<br />

One or more showers per week kept duff moist through<br />

mid-October after v>ich weather was drier and cooler<br />

than normal. The first mushrooms <strong>of</strong> ectomycorrhizal<br />

fungi in any <strong>of</strong> the stands developed oc the Surned<br />

plot. Subsequently the number <strong>of</strong> species on ~ne<br />

burned plot exceed that on the unbur2ed at each<br />

collectior, date. S~~ecies <strong>of</strong> these fungi were more<br />

numerous in the pungens/rigida plots compared with<br />

the virginianz plot through mid-September after which<br />

the naxirnuc: number <strong>of</strong> species varied betveer. one pine<br />

tpe an? the cther. Tinrough the end <strong>of</strong> Vovember when<br />

fruitir.6 ceesee, ??: <strong>of</strong> 12; prob:?.ie taxa <strong>of</strong> ect<strong>of</strong>ungi<br />

we?€ iacctifie? ES species ir. 25 genera <strong>of</strong><br />

3asl:ior;:cetes.<br />

J. C. l~A1,klER. 0. E;. MILLER, JR.. & C. CRUHN.<br />

Department <strong>of</strong> Biology, Virginia Polytechnic<br />

1nst.itutc & State University, Blacksburg. VA<br />

24060.<br />

Ectomycorrhizal fungi fruiting on burned and<br />

unburned pine plots after a long drought in<br />

the Virginia Appalachians.<br />

A third successive dry year was predicted for<br />

1988. Numerous lightening fires during 1987<br />

suggested the need for litter- and shrub-free<br />

firc brealrr on the Jefferson National Fnrest.<br />

In February one control burn for ,this purpose<br />

split a stand <strong>of</strong> Pinus pungens/P_. rigida with<br />

some oak into two plots <strong>of</strong> equal area. An-un-<br />

burned stand <strong>of</strong> Pinus virainiana with similar<br />

area but fewer oaks occupied a lower and more<br />

moist site. After a hot, dry six weeks, the<br />

first duff-moistening rain since mid-April<br />

fell on July 13. One or more showers per week<br />

kept duff moist through mid-October after<br />

which weather was drier and cooler than nor-<br />

mal. The first mushrooms <strong>of</strong> ectomycorrhizal<br />

fungi in any <strong>of</strong> the stands developed on the<br />

burned plot. Subsequently the number <strong>of</strong> spe-<br />

cies on the burned plot exceeded that on the<br />

unburned at each collection date. Species <strong>of</strong><br />

these fungi were more numerous in the pungens<br />

/rigida plots compared with the virginiana<br />

plot through mid-September after which the<br />

maximum number <strong>of</strong> species varied between one<br />

pine type and the other. Through the end <strong>of</strong><br />

November when fruiting ceased. 94 <strong>of</strong> 121<br />

probable taxa <strong>of</strong> ect<strong>of</strong>ungi were identified as<br />

species in 25 genera <strong>of</strong> Basidiomycetes.<br />

Ronald H; Petersen. Botany Department,<br />

University <strong>of</strong> -e, Knoxville, Th' 37996-<br />

1100. nat ing systems in the genus Xerom-<br />

phallus (Xerulaceae, Agaricales).<br />

Ut il izing single-spore Isolates, it was found<br />

that X, campanella, X. tenulpes, X. curtfpes,<br />

X; kauffmanji, and X; fulvipes are governed<br />

-<br />

-.<br />

by a unifactorial mating svstem. while X;<br />

caut icina? is and X, branneola show a bif aF<br />

torial syslem. In addition, "lethal" genes,<br />

caused hyphal lysis during hyphal confron-<br />

tation, operate in several taxa, and at least<br />

X. tenulpes is suspected <strong>of</strong> forming binuc-<br />

Gat-diospores. Biological species<br />

intercontinental distribut ion 1s discussed.


R. PINETTE, P. ZDROJOUY, AND S. BROWN.<br />

University <strong>of</strong> Naine at Presque Isle,<br />

Math/Science Division, 181 Main Street,<br />

Presque Isle, ME 04769.<br />

Effect <strong>of</strong> RoundupR, a glyphosate herbicide,<br />

on fi vitro growth <strong>of</strong> three species <strong>of</strong><br />

ectomycorrhizal fungi associated with black<br />

spruce.<br />

I n northern Raine, RoundupR, a glyphosate<br />

herbicide, is used to suppress undesirable<br />

species in black spruce plantations within<br />

the first year <strong>of</strong> transplanting seedlings.<br />

Three mycorrhizal species, Laccaria Laccata<br />

(Scop. ex Fr.) Berk 8 Br., Tylopi lus<br />

felleus (Fr.) Kars. and a Cortinarius sp.,<br />

were isolated from sporocarps associated<br />

ui th black spruce. These were tested for<br />

the effect <strong>of</strong> different concentrations (0,<br />

0.1, 1, 10, 100 and 1000 ppm) <strong>of</strong> the active<br />

ingredient, glyphosate, on the vitro<br />

growth <strong>of</strong> the isolates on Modified Melin<br />

Norkrans nutrient agar medium as measured<br />

by taking the diameter <strong>of</strong> the mycelium.<br />

Reduction i n growth due to different<br />

herbicide concent rations were evaluated<br />

using one-way ANOVA. Lover concentrations<br />

<strong>of</strong> glyphosate had a stimulatory effect, but<br />

higher concentrations resulted i n a<br />

significant (p=0.05) reduction in growth.<br />

M. J. POWELL and W. H. BLACKWELL. Department<br />

<strong>of</strong> Botany, Miami University, Oxford, OH<br />

45056. Analysis <strong>of</strong> zoosporic ultrastructural<br />

characters for phylogenetic reconstruction<br />

<strong>of</strong> Oomycetes.<br />

Current concepts on the classification and<br />

phylogenetic relationships <strong>of</strong> Protista are<br />

based on comparative ultrastructure <strong>of</strong><br />

motile spores. For the Oomycetes, data are<br />

accumulating on the ontogeny and detailed<br />

structure <strong>of</strong> zoosporic organelles,<br />

on organellar associations, and on the<br />

architecture <strong>of</strong> the flagellar apparatus.<br />

Even though these features have been<br />

compared empirically, characters and<br />

character states have not been scrutinized<br />

or analyzed using more objective methods.<br />

The purpose <strong>of</strong> this study is to collate<br />

existing ultrastructural data on zoospores<br />

<strong>of</strong> Oomycetes, to define characters and<br />

character states, and to analyze the data<br />

using cladistic methodology. Although<br />

there are readily identifiable gaps in<br />

the data set, analysis within Oomycetes<br />

supports the close affinity <strong>of</strong> the Order<br />

Leptomitales to the Saprolegniales. The<br />

order Lagenidiales does not hold together<br />

by character analysis, and hence<br />

represents a heterogeneous grouping <strong>of</strong><br />

organisms which should be realigned<br />

into different orders.<br />

R. H. PROCIDH and E. B. SMALLEX. lleprbmt <strong>of</strong><br />

Plant Pathology, University <strong>of</strong> Wisconsin, 1630<br />

Lirden m., Madison, WI, 53706.<br />

Effects <strong>of</strong> mnone E on the graJVl <strong>of</strong> ODhiostaM<br />

ulrni and other fungi.<br />

nEe deqree <strong>of</strong> phytoalexin toleranoe is an hprtant<br />

factor in limit- the virulenoe <strong>of</strong> sane funsdl<br />

pathagems: we the effects <strong>of</strong> the elm<br />

phytoalexln mansonone E on the myaelial qraJth <strong>of</strong><br />

Crhiostarna (ha.) Nand. an3 16 other fungal<br />

species to determine whether tolerance to mansomne<br />

E is important for virulence on elm. Mansomne E<br />

was incorporatad into potato dextrose agar at<br />

varicxls comtrations. Mansonone E inhibited the<br />

grwth <strong>of</strong> aggressive bola- <strong>of</strong> Q. more than<br />

that <strong>of</strong> nowaggressive isolates. O&iostasM<br />

was nure tolerant to mansonone E than were nost but<br />

not U,<strong>of</strong> the other fmqi ewmined.<br />

Ni-dine was used to generate mrtarrts <strong>of</strong> Q.<br />

ulmi with ' sensitivity to l~nsonone E.<br />

G 3 e h E w i t h varying degrees <strong>of</strong><br />

resistance to Q. u, were inoailated with these<br />

mutants, 3 mutants were less virulent than the wild<br />

type strain from which they were derived. Haever,<br />

the fcurth nutant was as virulent as the wild type<br />

strain. mese data suggest that alth0ql-I Q. ulrni is<br />

relatively tolerant to mansonone E, this tolerance<br />

may not be required for virulence on elm.<br />

C.C. PRUSSO. Biology Department, University <strong>of</strong><br />

Nevada. Reno. NV 89557.<br />

An interpretation <strong>of</strong> the mouth types <strong>of</strong> the<br />

Tulostoma basidiocarp.<br />

The mouth <strong>of</strong> the Tulostoma basidiocarp is one <strong>of</strong> the<br />

primary characters used in identifying collections to<br />

species. However, the variability encountered <strong>of</strong>ten<br />

makes selection <strong>of</strong> a mouth type difficult. Also,<br />

terms used to describe the mouth are based on inter-<br />

pretation that varies from author to author. During<br />

the preparation <strong>of</strong> a key to species <strong>of</strong> Tulostoma that<br />

occur in the Great Basin and Mojave Desert it became<br />

necessary to examine mouth types and to establish<br />

useable categories. Three mouth types are easily<br />

recognized. 1) The definite mouth is a circular to<br />

elliptical opening, plane extended into a tube <strong>of</strong><br />

varying length. 2) The fibrillose mouth has an open-<br />

ing surrounded by a hyphal mat built-up on the perid-<br />

ium. 3) The valvate mouth is formed by wedge-shaped<br />

segments that open upward in a stellate manner form-<br />

ing a crown-like rim. Other types are not as easily<br />

defined. The fimbriate mouth is an opening wfth<br />

fibrils projecting from the edge like a fringe. The<br />

rugose mouth is surrounded by a coarsely wrinkled,<br />

Flister-like border that is peridial in nature, not a<br />

build-up on the peridium. The indefinite mouth is<br />

quite varied and has no distinguishing characters,<br />

<strong>of</strong>ten being a mere slit or ragged opening. It may<br />

well be that the fimbriate and rugose types are forms<br />

<strong>of</strong> the indefinite.


S. C. REDLIN and A. Y. ROSSMAN. Systematic<br />

Botany and Mycology Laboratory, USDA-ARS;<br />

Beltsville, MD 20705. Cry~todiaporthe<br />

corni (Diaporthales) and its distinctively-<br />

pigmented anamorph.<br />

CrvDtodiaDorthe corni (Wehmeyer) Petrak is<br />

a pyrenomycetous teleomorph reported on<br />

Cornus spp. This fungus is associated with<br />

a twig blight and was collected on pagoda<br />

dogwood (cornus alternifolia L.) in the<br />

northern United States during investigations<br />

on dogwood anthracnose. h distinctive<br />

bright orange pigment produced in pure<br />

culture on several media was similar to the<br />

color observed on dogwood twigs containing<br />

ascocarps and conidion~ata. The anamorph<br />

was produced abundantly in cultures derived<br />

from single ascospores. MYXOSDO~~U~ nitidum<br />

Berkeley and Curtis is the earliest name for<br />

this anamorph, also known as Zvthia<br />

aurantiaca (Peck) Sacc. This study includes<br />

the first description <strong>of</strong> the fungus in pure<br />

culture and a redescription <strong>of</strong> the<br />

teleomorph and anamorph . Results indicate<br />

that Crv~todia~orthe corni is restricted to<br />

Cornus alternifolia. Characteristics <strong>of</strong> the<br />

growth in culture, the conidiomata, and the<br />

conidia differ significantly from the<br />

dogwood anthracnose fungus.<br />

STEF HEN REHNER and RYTAS VILGALYS. Dept. <strong>of</strong><br />

Botany, Duke University, Durham, N.C. 27706.<br />

Sequence evolution <strong>of</strong> the 25s nuclear<br />

ribosomal RNA subunit and phylogenetic<br />

analysis <strong>of</strong> the Agaricales<br />

Due to their universal occurrence and conserved<br />

structure, the nuclear ribosomal genes (rDNA) are a<br />

potential source <strong>of</strong> informative characters for<br />

inferring patterns <strong>of</strong> evolutionary relationships<br />

among the extant lineages <strong>of</strong> fungi. We describe a<br />

series <strong>of</strong> oligonucleotide primers developed for the<br />

polymerase chain reaction (PCR) to amplify<br />

ribosomal genes from fungi. The amplified rDNA<br />

can be used for restriction analysis, cloning, or<br />

nucleotide sequencing. Sequence analysis <strong>of</strong> the 5'<br />

half <strong>of</strong> the 25s genes <strong>of</strong> Microm~hale, Mvcena,<br />

Amanita, and &tharellus has revealed two modes<br />

<strong>of</strong> sequence evolution <strong>of</strong> rDNA in fungi, either<br />

through direct nucleotide substitution or length<br />

mutation. The picture that emerges is that the 25s<br />

ribosomal genes are comprised <strong>of</strong> conserved<br />

regions interspersed with more divergent domains,<br />

the latter <strong>of</strong>ten differing significantly in primary<br />

sequence and length. A data set <strong>of</strong> sequences from<br />

representatives <strong>of</strong> Agaric families will be<br />

presented and its use for evolutionary analysis will<br />

be discussed.<br />

-- Don R. Rrvnolds, Natural History Museum <strong>of</strong><br />

Los Angeles County. 900 Expositio~l<br />

Boulevard, Los Angeles, California 90007<br />

and John W. Taylor, Plant Biology<br />

Department, University <strong>of</strong> California.<br />

~erkele~, California 94720.<br />

Preliminary Observations Concerning a<br />

Phylogenetic<br />

Ascomycetes.<br />

Hypothesis for Ascostromatic<br />

The fungi <strong>of</strong> interest historically are known<br />

as the loculoascomycetes or bitunicate<br />

ascomycetes. A major problem' in the<br />

classification <strong>of</strong> these fungi, and its sister<br />

groups, is a lack <strong>of</strong> understanding <strong>of</strong> robust<br />

monophyletic groups. A phylogenetic<br />

hypothesis for loculoascomycetes sensu lato,<br />

as ascostromatic ascomycetes with a<br />

fissjtunicate, rostrate or extend-itunicate<br />

ascus, is being tested with molecular<br />

techniques and methods. Preliminary results<br />

from the study are reported.<br />

DNA sequencing is being carried out on DNA<br />

from pure culture isolates as well as from<br />

material obtained directly from nature and<br />

from herbarium collections. Sequencing data<br />

from the relatively large, evolutionary<br />

conservative, tandem, nuclear ribosomal.<br />

repeat DNA are being analyzed for<br />

confirmation <strong>of</strong> the monophyletic units<br />

discovered with macrocharacter analysis.<br />

P.L. RICHTER and J.M. BRUHN. School Of Forestry ard Uocd Products,<br />

Michigan Tuhnological University, noughton, Michigan 19931.<br />

Shifts in mycorrhizal fvlpus colonization <strong>of</strong> Pinus resinoss seedlings<br />

follwing outplanting.<br />

An ordered shift in mycorrhizal fmra colonization occurred on<br />

--<br />

Pinus resinosa Ait. seedlings wtplanted on three recently cleared<br />

northern hardwwd sites in the Uppr Peninsula <strong>of</strong> Michigan. The shift,<br />

related to seedling mge fran ourplmting, was demonstrated by<br />

quantification <strong>of</strong> nycorrhizml mrphology types, lsboratory isolation <strong>of</strong><br />

fmgi fran mycorrhizee, phy$iological categorization <strong>of</strong> fmgi recovered<br />

frun ycorrhizae, and surveys <strong>of</strong> fruiting bodies associated with<br />

seedlings. Uith increasing plantation age, 1) the -r <strong>of</strong><br />

nomncorrhizal root tips encantered declined to zero. 2) the cannon<br />

nursery ysorrhizae decreased in abnd.nce, 3) m wcorrhizal types<br />

(especially Cmococcrn md u) k c m more abundant, 4)<br />

cellulolytic f w i (in part representing ectmjomycorrhizal fungi)<br />

uere isolated fran nycorrhizae less frequently, while 5)<br />

utomycorrhizal f w i uere isolated from mycorrhizae more fr-tty.<br />

The nvrber <strong>of</strong> apparently different mycorrhizal f w species isolated<br />

fran mycorrhizae increased fran 5 in the first year after outplanting<br />

to 22 in the fwrth year.<br />

The squcnce <strong>of</strong> ycorrhizal funpi Colonizing red pine seedlings from<br />

nursery to four years follwing outplanting was as follows. Ectcndo-<br />

wcorrhizal fmgi. Thelechora terrestris, md Laccaris laccata uere<br />

present on nursery seedlings. Ectendaycorrhizal fungi nave wy to<br />

further colonization by utnycorrhizal f w i soon after outplanting.<br />

1. terrestris and 1. Iaccata persisted on outplated seedlings, but<br />

allowed colonization by g. geophilun and L. bicolor during the first<br />

year. The Latter tw cpecies increased (n abundance on seedlings,<br />

while gt&& spp. appeared bring the sued year. Lactarius spp.<br />

appared during the third year, and llekluna sw. appeared during the<br />

fwrth year. ALmg uith the major ptners Listm above, additiarsl<br />

unidentified ectcmycorrhizal fmgi (possibly species <strong>of</strong> m,<br />

Boletus, Rhizooogon, etc.) formed mycorrhizse with seedlings,<br />

especislty during the third end fourth year after outplanting.


R.W. ROBERSON. Department <strong>of</strong> Botany, Arizona State Universiry,<br />

Tempe, AZ 85287. Microscopic observations <strong>of</strong> teliospore germination<br />

<strong>of</strong> Gymnosporat~~urn clavipes.<br />

Cytological features <strong>of</strong> germinating teliospores <strong>of</strong> the common rust<br />

fungus Gymnosporangium clavipes Cke. & Pk. were examined using<br />

tight and transmission electron microscopy, LM and TEM respectively.<br />

LM observations <strong>of</strong> living cells were made using Nomarski optics.<br />

Developmental changes in the microtuhule and actin ~oskeletoas and<br />

nuclear migration were examined in fied cells stained for<br />

epifluorescenu: microscopy. For TEM, geminating teliospores were<br />

cry<strong>of</strong>ued by high pressurc freezing or h!, rapidly plunpg spores into<br />

liquid propane followed by Irewe suhsrirution. Mature teliospores <strong>of</strong><br />

G. clavipes consisted <strong>of</strong> an apical and basal ell separated by a septum.<br />

Each cell contained a single diploid nucleus. Golgi bodies were<br />

identified as enlarged cistemae <strong>of</strong> varying shape& sizes and elearon<br />

opacities. Mitochondria werc present throughout the cytoplasm <strong>of</strong> the<br />

germinating teliospore. Smooth endoplasmic reticulum was closely<br />

associated with mitochondria. Additional components <strong>of</strong> the cytoplasm<br />

included multivesicular bodies, glycogen, Lipid bodies and vacuoles.<br />

Teliosporcs contained two germ pore regions, one located at the apical<br />

end and the other at the basal end. Upon germination a single germ<br />

tube emerged from the germ pore region. The germ tube exhibited a<br />

polarized mode <strong>of</strong> cellular powth that occurred through apical<br />

expansion. Cytoplasmic vesicles were obsemd in the apical region <strong>of</strong><br />

elongating germ tubes. Immun<strong>of</strong>luorescence techniques revealed<br />

abundant microtubules generally oriented parallel to the long axis <strong>of</strong><br />

the germ tube. Actin staining showed an accumulation <strong>of</strong> brightly<br />

fluorescent plaques in peripheral regions <strong>of</strong> the germ tube. The<br />

prophase nudeus migrated into the germ tube where it divided<br />

meiotically. Septa divided the germ tube into four uninucleate cells.<br />

Each cell than gave rise to a single sterigma and a haploid, biiucleate<br />

basidiospore.<br />

D. W. ROBERTS and A. E. HAJEK. Insect Pathology<br />

Resource Center, Boyce Thompson Institute, Tower<br />

Road, Cornell University, Ithaca, NY 14853-1801.<br />

Entomopathogenic fungi as bioinsecticides.<br />

The entomopathogenic fungi are an extremely diverse<br />

group taxonomically and include species which attack<br />

virtually all groups <strong>of</strong> economically important<br />

insect pests. Programs are underway worldwide co<br />

exploit these organisms as supplements or<br />

alternatives to synthetic chemical insecticides.<br />

Use patterns vary from classical colonization to .<br />

massive introductions <strong>of</strong> inoculum similar to amounts<br />

used for chemical insecticides. Fungi seem to be<br />

particularly promising for use against forest,<br />

pasture/forage, and soil (particulary sandy soil)<br />

insect pests. Current research efforts include<br />

molecular biology studies to understand mechanisms<br />

underlying pathogenesis and to improve fungal<br />

strains, studies co discover and evaluate fungal<br />

toxins, as well as some very promising studies on<br />

understanding fungal epizootics wich the goal <strong>of</strong><br />

predicting and initiating them.<br />

R. A. RE.PEX anC S. C. C&SSAR. Departr;rent <strong>of</strong><br />

Biclq>, College, hlma, MI 48801. A new<br />

species <strong>of</strong> ~rosiella associated with the<br />

ambrosia beetle ::ylekms obesus (Colecptera:<br />

Scoly~idae ) .<br />

19.-1.2 Wtle >:. dsus infests m3t deciduous<br />

trees withi; its ranae <strong>of</strong> the eastern United<br />

States ant Cans&. 'his stu@.y !$as conciuct&.<br />

u~ 5. obesus ettacl-hq tdn6-thrm or cut<br />

as- lgs in Central blichigm. l'lm sole<br />

fungal syrbiont. oi . &SU bas fad to bE<br />

undescribed m!rkr <strong>of</strong> the Mrfect pnus<br />

Mrosiella. me fungus will be characterized<br />

fran rrorpholqical and cultural studies. me<br />

fungus was consistently isolated as the sole<br />

micro?Je fran the mmotal mycangiun <strong>of</strong> the<br />

fen-ale beetles collected either in flight or<br />

fmn early stages <strong>of</strong> construction <strong>of</strong> the<br />

gallery system. The fungus proliferated £ran<br />

the mycangiun and was spread by the baring<br />

i?ctivit:r <strong>of</strong> t! parental adult. At the time <strong>of</strong><br />

miposition by the beetle the fungus f& a<br />

monoc1ilt~up upcsl the walls <strong>of</strong> the gallery and<br />

was exclusively fed upon by the developing<br />

larvae. When beetle pupation occurred the<br />

fun@ layer was slr;ost entirely consum&, but<br />

regre: in d l patches to be reinoculated into<br />

the mycangia <strong>of</strong> young progeny adult females.<br />

S.O. ROGERS, S.A. REHNER, J .F. A??RATI AND<br />

C. BLEDSOE, College <strong>of</strong> Environmental Science and<br />

Forestry, SUNY, Syracuse, NY 13210, Department <strong>of</strong><br />

Botany, Duke University, Durham. NC 27706. Botany<br />

Department, University <strong>of</strong> Washington, Seattle. WA<br />

98195 and College <strong>of</strong> Forest Resources, University <strong>of</strong><br />

Washington, Seattle, WA 98195.<br />

Coarse and fine scale restriction enzyme mapping <strong>of</strong><br />

the ribosomal DNA units from Basidiomypetes.<br />

The ribosomal DNA repeat units fran over 200 speci-<br />

mens (over 80 species from 48 genera) representing<br />

22 families <strong>of</strong> Basidimycetes have been mapped using<br />

from one to four restriction enzymes (that have six<br />

base pair recognition sequences). A composite map<br />

that indicates the variable and conserved regions<br />

was constructed. The spacer regions exhibited the<br />

greatest variation. Parts <strong>of</strong> the genes exhibited<br />

moderate variability, while certain portions were<br />

well conserved. An intron may be present in the 3'<br />

region <strong>of</strong> the 255 gene in at least six genera (from<br />

three families). Several portions <strong>of</strong> the repeat are<br />

being amplified using PCR. These were digested with<br />

restriction enzymes that have four base pair recog-<br />

nition sequences.to construct fine structure maps <strong>of</strong><br />

the amplified regions. Representatives <strong>of</strong> each<br />

clearly defined taxonomic group are to be sequenced.<br />

These data are being used in phylogenetic and tax-<br />

onomic studies <strong>of</strong> the Basidiomycetes. Additionally,<br />

the molecular characters derived from the work are<br />

being used to identify mycelial cultures and<br />

mycorrhizae from lab and field collected specimens.


A. I. ROYEKC. Departamenro oe Ciencias Biolbgicas,<br />

I'aculrai at Ciencias Lxactas y Iisturales, Universi-<br />

dad de Buer)os kires. 1L2& Buenos Aires, Argentina.<br />

Wood and bar^ innabiting nicromycetes on Eucalyptus<br />

viminalis from Argentink.<br />

During a 2 years floristic and ecological survey <strong>of</strong><br />

micromycetes on stumps <strong>of</strong> Eucalyptus viminalis, in<br />

the province <strong>of</strong> Buenos Aires, Argentina, 1920 samples<br />

were collected. To find out what Ascomycetes<br />

occu- or, this s\lhstrat.e WRP the first objetive. So<br />

far 63 species <strong>of</strong> kscomycetes and 62 species <strong>of</strong> Deuteromycetes<br />

are identified. Most <strong>of</strong> them are new records<br />

for Argentina, some are new genera and species<br />

and a number <strong>of</strong> them are still unidentified. These<br />

.~esults were compared with the world-wide record <strong>of</strong><br />

'species found on Eucalyptus spp., kept at IMI, and<br />

only 35% <strong>of</strong> the 125 species registered through the<br />

present work are mentioned in that list. Some <strong>of</strong> the<br />

more distinct species will be shown.<br />

J. C. ROYER and P. A. HORGEN. Center for Plant<br />

Biotechnology, University <strong>of</strong> Toronto.<br />

Towards the development <strong>of</strong> a transformation system for<br />

Aparicus bisporus.<br />

The slow growth rate <strong>of</strong> A. bisporus presents an obstacle in the<br />

generation <strong>of</strong> large amounts <strong>of</strong> actively owing mycelium<br />

required for efficient protoulasr generation. This problem has<br />

been overcome through the use <strong>of</strong> repeated inoculum build-up<br />

<strong>of</strong> snain ATCC 24662, a relatively fast growing homokaryon.<br />

Our optimized procedure for protoplast formation involves<br />

incubation <strong>of</strong> mycelium from a 2-3 day old tertiary culture with<br />

Novozyme 234 (10 mgtrnl) in MgSOq (0.8 M, pH 4.3) for 45<br />

min with gentle shaking. Approximately lo9 protoplasts are<br />

typically liberated from a la) ml culture. Protoplast<br />

regeneration rates have been increased approximately 50-fold<br />

(to approximately 2.0 5'0) by subsdtuting sucrose (0.6 M) for<br />

sorbitol in the regenention medium. Several plasmid vectors<br />

which have been used to transform a dlverse goup <strong>of</strong><br />

filamentous fungi to hypmycin resistance, dong with a<br />

Dromoter librarv <strong>of</strong> A. bisporus fragments fused to a<br />

hvgromycin re$stance gene from z. coli have been<br />

unsuccessful in transforming A. b~sporus using a variety <strong>of</strong><br />

transformation procedures. These data and similar results<br />

with closely related basidiomycetes have resulted in a working<br />

hypothesis that bacterial genes may not be expressed in A.<br />

bisporu, even when fused with fungal promoters. Recent<br />

experiments utilizing fungal genes wluch <strong>of</strong>fer the potential to<br />

complement auxotrophc mutations or alter nunitional<br />

capability will be dscussed.<br />

5. J. and K. A. SElfERT. Systmtic Botany and llycolw<br />

Laboratory, USDA, Urn. 304, B-OIlA, Beltsvi:le, WD 20705 and Forintek<br />

Canada Corp., Ottawa, Ontario KIG 325. Reassessment <strong>of</strong> species<br />

attributed to Gliocladiun.<br />

;Gliocladiun is the traditional genus for hyphmcetes that have<br />

rolorless to light-colored, penicillately branched conidiophores, and<br />

slimy, amerosporws conidia. These characters do MI necessarily refut<br />

phylogeny. CLassificatim <strong>of</strong> anarorphic fungi will be natural only uhm<br />

tit reflects classification <strong>of</strong> tho respective releomorphs. Telwrphs<br />

hoving amrphs classified in Gliocladim are fouvl in five genera <strong>of</strong><br />

xhe Hypocreales: Hmcrea, -, Ncctrioosis, Rounenueriell?, erd<br />

6phaerostilbr:A. G!ioclar!lm anamrphs are not kmm outside the<br />

dywc-e~les, b'though tnere are svecies that have not vet beep. lin~ed tc<br />

trlecmorphs. Species rk G!iorladiv. can be distrituted am- five<br />

distinct anamorph, genera w!.t7 their teleomorphs are considered. S:ccies<br />

sivilar to 5. pnicillioides, the type specles, are ananorms <strong>of</strong><br />

Schaerostilblla and Rmqueriella. SDheerostilbella is emended to<br />

.~nclude Hmcrea species centered on i. =I-. Rmswriella is a<br />

cleistothec~al genus <strong>of</strong> urertain affinities in the order. Gliocladiun<br />

virens and similar anamrphs can be include;: in Trichodem; they are<br />

correlated only to green-spored Hmcres species centered on i.<br />

pelstinosa. Gliocladivn U d e (= G. deliaurscens), the anemorph <strong>of</strong> H.<br />

- lutea, can perhaps be reclassified in Gloiosphacra; it is distinct from<br />

Trichoderma. Gliocladiun roseun. the arwmorph <strong>of</strong> Hrctria ochroleuca, is<br />

s species <strong>of</strong> Clonostschys. The taxomic affinities and taxortunic<br />

placement <strong>of</strong> the Gliocladiun arwmorph <strong>of</strong> Nectrio~sis swran~iicola are<br />

still unclear.<br />

eeggll- Department <strong>of</strong> Botany, Duke University,<br />

Durham, NC, 27706. Grazing preferences <strong>of</strong> two<br />

collembolan species, Folsomia candia and proisotoma<br />

minuta, for ectomycorrhizal fungi.<br />

The purpose <strong>of</strong> this study was to determine if two species<br />

<strong>of</strong> Collernbola, Folsornia candida and Proisotoma minuta,<br />

graze preferentially on ectomycorrhizal fungi. 1. candida<br />

preferences for fifteen ectomycorrhizal fungi were initially<br />

tested using a 4x4 balanced lattice design. leccinum<br />

scabrum, the most preferred fungi and Melanooaster<br />

Uberitorrnis, the least preterred fungi were the only<br />

choices that differed significantly in the number <strong>of</strong> visits by<br />

- F. candida. Pairwise comparisons <strong>of</strong> preferred and less<br />

preferred fungi were then performed with both E. andida<br />

and P. minuta. Both E. candida and P. rninuk preferred<br />

Gautieria otthii over 1. scabrum, AIoova plivaceotinctu~ or<br />

M. Uberiformi~. The grazing preferences exhibited by E.<br />

candida and P. minuta in this study were not taxonomically<br />

based nor based on familiarity with the food source.<br />

Preterence is most likely due to some property <strong>of</strong> the fungi.<br />

This study suggests that collembolan grazing may<br />

differentially affect plants associated with ectomycorrhizal<br />

fungi depending on whether they are associated with<br />

preferred or less preferred fungal species.<br />

ME-AE SEO and R. C. ANDERSON. Department <strong>of</strong><br />

Biological Sciences. Illinois State University,<br />

Normal, IL 61761.<br />

Effects <strong>of</strong> soil microbial and mycorrhizal<br />

associations on the productivity and photosynthetic<br />

rates <strong>of</strong> Panax auinauefolium L.<br />

The purpose <strong>of</strong> this study was to determine the<br />

effect <strong>of</strong> mycorrhizal colonization and soil<br />

organisms on the productivity <strong>of</strong> a shade adapted<br />

plant, <strong>America</strong>n ginseng (Panax guinauefolium L.).<br />

Germinated seeds were planted in three substrates<br />

(1) non-autoclaved soil, (2) autoclaved soil to<br />

which mycorrhizal inoculum was added, and (3)<br />

autoclaved soil which received a VAM (vesicular-<br />

arbuscular mycorrhizal) -free filtrate <strong>of</strong> non-<br />

autoclaved soil. Plants were grown in the field<br />

under 10% <strong>of</strong> full sunlighr for one growing season.<br />

Meah total biomass, shoot weight, and phocor-ynthetic


ates <strong>of</strong> ginseng plants grown in the non-autoclaved<br />

soil and the autoclaved soil receiving mycorrhizal<br />

inoculum were significantly (p


P. L. SKATRUD, J. HOSKINS, J. D. WOOD, M. B. TOBIN<br />

and S. W. QUEEKER. Lilly Research Laboratories,<br />

Lilly Corporate Center, Indianapolis, IN 46285<br />

Genetic manipulation <strong>of</strong> the $-lactam antibiotic<br />

biosynthetic pathway.<br />

The p-lactam antibiotics, which include the<br />

penicillins and cephalosporins, all share certain<br />

structural features, a similar mode <strong>of</strong> action and<br />

a lov toxicity pr<strong>of</strong>ile. Recently, several genes in<br />

the biosynthetic pathways leading to b-lactam<br />

production have been cloned and characterized. As<br />

a result <strong>of</strong> these studies, specific rational<br />

alterations <strong>of</strong> the biosynthetic pathway in<br />

industrially-important . . producing - organisms -<br />

.JCephalosporium acremonium and Penicillium<br />

Phrysogenum) are now possible. Three specific<br />

applications <strong>of</strong> genetic alteration <strong>of</strong> the<br />

biosynthetic pathway will be discussed: 1. Gene<br />

dosage studies leading to increased overall<br />

productivity. 2. Gene disruption studies leading<br />

to inactivation <strong>of</strong> specific genes. 3. Expression<br />

<strong>of</strong> a foreign gene in the $-lactam producing fungus<br />

- P. chrysogenum leading to production <strong>of</strong> an altered<br />

$-lactam structure in fermentation.<br />

-- K.T. - SMITH. USDA Forest Service, P.O. Box 640, Durham, NH<br />

03824. The moisture content <strong>of</strong> wood is altered by Postia<br />

placenta and Trametes versicolor early in the decay process.<br />

The wood<br />

-<br />

decay process requires appropriate levels <strong>of</strong> moisture<br />

and aeration. The decay fungi are capable <strong>of</strong> altering<br />

these levels. Various combinations <strong>of</strong> decay fungi and wood<br />

species were tested to determine their effect on wood moisture<br />

content (MC). Decay cnambers were french-square bottles,<br />

each containing an agar culture <strong>of</strong> either the brownrot<br />

fungus placenta (Fr.) M. Larsen & Lombard, the<br />

whiterot fungus Trametes versicolor (L:Fr.) F'ilat (syn. Coriolus<br />

versicolor (L.:Fr.) Quel.!, or uninoculated agar. Oven-dried<br />

wood samples (5 x 10 x 50 mm, radial: tangential: longitudinal)<br />

were prepared from hardwood and s<strong>of</strong>twood trees differing<br />

in decay resistance and were placed in the cham- .<br />

bers. Within one or two weeks <strong>of</strong> incubation, the brownrot<br />

fungus caused greater increases in wood MC than did the<br />

whiterot fungus. Both fungi increased wood MC above that<br />

<strong>of</strong> the uninoculated controls. This pattern was maintained at<br />

12 weeks <strong>of</strong> incubation and was correlated with the severity<br />

<strong>of</strong> decay measured as percent weight loss. Across the tree<br />

species tested, as wood increased in decay resistance, the<br />

ability <strong>of</strong> the fungi to wet the wood decreased. In some fungus<br />

and wood combinations, wood MC may have become<br />

sufficiently high to limit the aerobic respiration <strong>of</strong> the wood<br />

by the fungi. This possibility draws attention to the need for<br />

the careful choice <strong>of</strong> appropriate experimental conditions to<br />

test comparative decay resistance.<br />

M.L. SMITH and J.B. ANDERSON. Dept. <strong>of</strong> Botany.<br />

University <strong>of</strong> Toronto, Erindale College. Mississauga.<br />

Ontario, Canada L5L 1C6<br />

Mitochondria1 genetics in a natural population <strong>of</strong><br />

Wc have examined the transmission and propagation <strong>of</strong><br />

mitochondrial genotypes in natural clones <strong>of</strong> asmill aria<br />

at a nonh Michigan hardwood forest study site. Through<br />

an analysis <strong>of</strong> mating-type alleles we have determined<br />

that therc are two A. bulbosa clones. each exceeding 500<br />

m diameter, at the sitc. In addition. there are several<br />

smaller A. DsIoYae clones within a 9,000 m2 red pine<br />

plantation, locatcd within the hardwood stand. Based on<br />

rcstriclion fragment length polymorphisms (RFLPs)<br />

each vegetative clone at the site has one. unique<br />

mitochondrial DNA type. In contrast, a diploid mycelium<br />

arising from a compatible laboratory mating <strong>of</strong> haploid<br />

monokaryons , contains mitochondria from both parents<br />

since nuclei, but not mitochondria, migrate<br />

bidirectionally. Experiments now underway are<br />

designed to dctermine the nature and origin <strong>of</strong><br />

intraspecific variation <strong>of</strong> the mitochondria1 genome in<br />

Arm i l l ari a species. Through RFLP and nucleotide<br />

sequence analysis we are attempting to detect intraclonal<br />

polymorphisms between distant regions <strong>of</strong> the very old<br />

(ca 400 to 900 yrs) A. bulbosa clones at the Michigan site.<br />

By comparing RFLP maps from several A. Dstovag clones,<br />

we will determine where mutations are likely to occur in<br />

thc mtDNA molecule.<br />

Fred S~iesel, Department <strong>of</strong> Botany and<br />

Bacteriology, University <strong>of</strong> Arkansas,<br />

Fayetteville, AR 72701.<br />

Evening Discussion I. Federal Funding for<br />

<strong>Mycological</strong> Research. James Rodman,<br />

Systematic Biology, National Science<br />

Foundation, Washington, DC. Fundinu Throush<br />

the NSF. David Malloch, Department <strong>of</strong><br />

Botany, University <strong>of</strong> Toronto, Toronto,<br />

Ontario, Canada. Fundins Throuuh NSERC. A<br />

Canadian Point <strong>of</strong> View. Harold Keller,<br />

University <strong>of</strong> Texas, Arlington, TX. what to<br />

EXDeCt <strong>of</strong> Your S D O ~ S Prourams O ~ ~ ~ Office. A<br />

representative, NIAID, Division <strong>of</strong><br />

Microbiology and Infectious Diseases,<br />

Beltsville, MD. Fundinu Throuqh the NIH.<br />

F.W. SPIEGEL. Department <strong>of</strong> Botany and<br />

Microbiology, University <strong>of</strong> Arkansas,<br />

Fayetteville, AR 72701.<br />

Revision <strong>of</strong> the genus Protostelium.<br />

The mycetozoan genus Protostelium contains<br />

six described species: P. mycopha~a, 2.<br />

nocturnum, P. irre~ularis, 2. expulsum, z.<br />

pvriformis, and 2. arachis~orum. All these<br />

organisms meet the present morphological<br />

criteria for inclusion in the genus. That<br />

is, they all have a trophic state that<br />

consists <strong>of</strong> uninucleate, nonflagellate<br />

amoebre, and they all have sporocarps which


have single, deciduous spores on the tip <strong>of</strong><br />

a delicate stalk. However, these<br />

characters are not well defined, and<br />

characters based on amoeba1 morphology and<br />

ultrastructure, sporocarp development, and<br />

fruiting body structure suggest that the<br />

genus should be divided into three separate<br />

genera. The genus Protostelium would<br />

retain P. mycophaga, the type species, P .<br />

nocturnum, and Y. pyriformis. A new genus<br />

will have to be established for P.<br />

irregularis and P. expulsum, and 2.<br />

arachisporum should be reassigned to the<br />

genus Endostalium. Protostelium S.S. and<br />

the new genus appear to be members <strong>of</strong> the<br />

monophyletic group that includes the<br />

flagellate protostelids and myxomycetes,<br />

while Endostelium is not closely related.<br />

PETER D. STAHL and MARTHA CHRISTENSEN. W. K.<br />

Kellogg Biological Station, Michigan State University, Hickory<br />

Corners, MI 49060 and Department <strong>of</strong> Botany, University <strong>of</strong><br />

Wyoming. Laramie, WY 8207 1.<br />

In Vitro interactions among members <strong>of</strong> a soil micr<strong>of</strong>ungal<br />

community<br />

Interactions <strong>of</strong> four prominent and three rare species <strong>of</strong> fungi<br />

isolated from soils at the Konza Long Term Ecological Research<br />

Sire were examined and characterized. Pairs <strong>of</strong> fungi were<br />

grown on malt agar at varying distances apart and observed for<br />

up to four weeks. The growth <strong>of</strong> six <strong>of</strong> the seven species was<br />

inhibited to some degree in the presence <strong>of</strong> each other fungus.<br />

Growth <strong>of</strong> the excepted species was stimulated in the presence <strong>of</strong><br />

five <strong>of</strong> the other fungi. Cessation <strong>of</strong> growth at contacting colony<br />

perimeters occurred in 57% <strong>of</strong> the pairings, mutual arrest at a<br />

distance was observed in 18% <strong>of</strong> the tests and continued growth<br />

<strong>of</strong> one colony into the other occurred in the remaining 2590 <strong>of</strong> the<br />

interactions. No correlation was found between prominence or<br />

rarity <strong>of</strong> a species in the community and its response in paired<br />

interactions. Our observations and those <strong>of</strong> others suggest that<br />

while overall composition and structure in soil m:cr<strong>of</strong>ungal<br />

communities can be'multifa~toriall~ related to vegetation and soil<br />

~hvsical . - and chemical factors, species interactions may<br />

significantly influence ~om~ositionwiihi- microsites.<br />

M. M. STANKIS~, C. A. SPECHT*. L. CIASSON~, C. P.<br />

NOVOTNY' and R. C. ULLRICH~. Departments <strong>of</strong><br />

Microbiology and Molecular cenetics1 and Botany2,<br />

University <strong>of</strong> Vermont, Burlington. VT 05405.<br />

A molecular analysis <strong>of</strong> the & mating-type locus <strong>of</strong><br />

~chizo~hvllum commune.<br />

The Basidiomycete Schizo~hvllum commune<br />

(Aphyllophorales, Schizophyllaceae) is a model<br />

system for the analysis <strong>of</strong> genes controlling mating<br />

interactions and sexual development in the higher<br />

fungi. Mating betveen homokaryons is controlled by<br />

four genes: &, u, & and M, each <strong>of</strong> vhich is<br />

multiallelic. Three alleles <strong>of</strong> ,& have been<br />

isolated: u. and a. The a and &<br />

fragments sequenced to date shov no DNA sequence<br />

similarity to one another. Sequence data available<br />

from the Aa3 fragment reveals some degree <strong>of</strong><br />

similarity to both &a1 and Aa4. 'Iransla~ion cf<br />

open-reading-frames from corresponding "start"<br />

signals in and & generates an amino acid<br />

sequence in vhich there is 48% identity <strong>of</strong> the<br />

first 80 amino acids. Comparison <strong>of</strong> the sequences<br />

<strong>of</strong> end && vith intron consensus sequences<br />

suggests that each contains an intron. Translation .<br />

<strong>of</strong> the spliced transcripts <strong>of</strong> each yields<br />

polypeptides that shov an additional region <strong>of</strong> 46%<br />

amino acid identity tovards the C-terminus. This<br />

region contains a motif related to the homeodomain<br />

cf genes vhich are known to regulate development in<br />

eukaryotes. No homeodomain has been identified in<br />

any open-reading-frame present in u.<br />

& STRATTON, Biology Department, Princeton<br />

University, Princeton, New Jersey 08544 USA.<br />

Genetics and population structure <strong>of</strong> Ustilaeo<br />

violacea.<br />

The fungal pathogen Jlstilaeo violacea is widely<br />

distributed in Europe; in the USA it is limited to<br />

southwestern Virginia, although its host (Silene<br />

-) is common throughout the eastern US. Spore<br />

dispersal among populations has been estimated by<br />

yearly censuses <strong>of</strong> disease incidence in roadside<br />

populations <strong>of</strong> Silene alba. Electrophoretic studies<br />

showed little alloz~e variation in violacea.<br />

Isolates fror. 7 Virginia populations were monomorphic<br />

at 17/18 allozyme ioci. The single polymorphic<br />

enzyme locus (MDH) is closely linked to the mating<br />

type locus, for which all individuals are necessarily<br />

heterozygous. The polymorphism is probably<br />

maintained via hitchhiking. In contrast, DNA markers<br />

show much higher levels <strong>of</strong> polymorphism, both within<br />

and among populations. RFLP markers were used to<br />

estimate population structure and mating system<br />

parameters <strong>of</strong> this natural plant pathogen. In<br />

addition, the genetic markers allow comparison <strong>of</strong><br />

transmission rates <strong>of</strong> isolates in experimental<br />

populstions. A second sympatric species <strong>of</strong> Ustilaeo<br />

infects the native Silene vireinica. Ustilaeo from<br />

the two host plants show fixed allelic differences at<br />

5 enzyme loci, even when isolates were collected


exposure to fungi via an inuoductory microbiology class.<br />

Almost all limit use <strong>of</strong> fungi in the HS curriculum to a week or<br />

wo during an organismic biology survey. As pan <strong>of</strong> each<br />

Institute, teachers were insrmcted in mycology and related<br />

laboratory skills. That fungi can be used a11 vear to teach<br />

biological principles via hands-on laboratories was stressed.<br />

Due to variations in Institute design. teachers received<br />

mycology insrmction for (a) two Saturday 11'2 day workshops,<br />

(b) three 2-day weekend workshops, or (c) a full summer<br />

session. Evaluations and post-lnstitute comments indicate all<br />

periods were useful. But, summer sessions provided more<br />

nme to develop skills. c q out (rather than just discuss)<br />

laboratory exercises, and develop creative lessons for<br />

integration into the HS cuniculum. Since each HS teacher<br />

contacts about 3.250 students in a 25 year career and if MSA<br />

wants to stimulate more interest in mycology, more outreach<br />

programs emphasizing hands-on experience with fungi should<br />

:& available to current HS biology teachers.<br />

R.S. SURVE and G.C. ADAf1S. Department <strong>of</strong> Botany<br />

and Plant Pathology, Michigan State University,<br />

East Lansing, MI 48824. Phenetic groups within<br />

Leucostoma persoonii and I. cincta based on Allozyme<br />

Analysis.<br />

Teleomorphs <strong>of</strong> Leucostom ersoonii and L. cincta<br />

were collected on six u s spp. and Malus pumila<br />

in North <strong>America</strong>. These isolates and isolates<br />

from perennial cankers with the Leucocytospora<br />

anamorphs were compared using allozyme polymorphisms.<br />

Pol ymorphi sms at ten enzyme 1 oci were revealed<br />

by cellulose acetate gel electrophoresis, these<br />

included phosphopl ucoi somerase, ma1 ate dehydrogenase,<br />

gl ucose-6-phosphate dehydrogenase, phosphogluconutase,<br />

phosphoglucodehydrogenase, ma1 ic enzyme,<br />

manni to1 dehydrogenase, gl utamate dehydrogenase,<br />

isocitrate dehvdroaenase and hexokinase. A1 lozme<br />

patterns <strong>of</strong> ~e;cocytospora isolates having cul tuial<br />

characteristics 1 i ke L. ersoonii formed twc;<br />

distinct phenetic orouD~nqs. h o u p was widespread<br />

and was ccrrelated with the teleomorph.<br />

The second group occurs in Michigan in the same<br />

orchards as the first group but it has not yet<br />

been correlated with a know teleomorph. The two<br />

groups were distinct from all phenetic groupings<br />

within I. cincta. Allozyme patterns <strong>of</strong> I. cincta<br />

formed three phenetic groupings, a distinct group<br />

on and two related groups on Prunus. The<br />

three groups are each correlated with teleomorphs.<br />

The morphology <strong>of</strong> the ascomata <strong>of</strong> the three grouos<br />

appears identical but the groups differ in culturcl<br />

characteristics and temperature optima for growtn.<br />

J. B. SUEEFLzU\i, A. L. SELBT, J. P. FREETIAN, P. P.<br />

FU, D. K. fi"ELLER, and. C. E. CERNIGLW. National<br />

Center for Toxicolcqical Research, Food and Drug<br />

Pdninistration, Jefferson, A! 72079. MetdD3li.m <strong>of</strong><br />

anthracene by Fhizocmnia soiani.<br />

?he tricyclic armtic hydrocarmn anthracene, an<br />

enviromtal poliutant, has been use6 to indicace<br />

probable contaminaL2on by plycyclic armatlc hycko-<br />

carhns (PAHs). We have investiqatd the mtzdmlisr,<br />

35 anLthxacene by a SL--ai? <strong>of</strong> Fkizgtonia sola71. Tne<br />

funqus was qm for p &+rs at 2;'C L~ a l q~lc<br />

medium containing mlt extract and glucose and saturated<br />

with anthracene. After the culture medium had<br />

been extracted with ethyl acetate, high-perfomce<br />

liquid chmtcgraphy and thin-layer chrcxnatcqraphy<br />

were used to separate the principal anthracene<br />

metabolites. The metabolites were identified by<br />

analysis <strong>of</strong> their spectral data, including ultraviolet<br />

absorption, mass, and nuclear mcmetic<br />

resonance sp&tra; Fhizoctonia solani &t&olized<br />

anthracene prinrarily at the 1,2-positions to form<br />

1,2-dlhydroxy-lt24ihydroanthracene; both cis and<br />

trans imwrs were formed. The circular dichroisn<br />

spectrum <strong>of</strong> the e-1,2+ihydrodiol indicated that<br />

the prebmimnt enanticmer ha6 an absolute colrfiguration<br />

<strong>of</strong> (-)-152s. Tnis configuration was the same<br />

as that <strong>of</strong> the principal enantim produced by<br />

Cunninghamella elegans and consequently differed frun<br />

that repted for mmmlian enzyes. A conjugate <strong>of</strong><br />

1,2-dihydroxy-1,2-dihy-thracene with a sugar<br />

residue was also detected. Tnus, g. solani first<br />

metabolized anthracene to lI2-dihydroxy-1, 24ihydroanthracene<br />

and then conjugated the dihydrcdiol with a<br />

sugar.<br />

T. TALOU, F:. DBLMAS and A. CASET. Laboratoirede mimic<br />

des Agroressources, Ecoie de Chimie de Toulouse,<br />

118 route de Narbonne 31077 Toulouse Cedex FRANCE.<br />

Aroma voiatiles analysis : a feasable approach for<br />

chenlotaxonomic determination <strong>of</strong> truffles.<br />

Truffles are undergroung mushrooms that grow in symbio<br />

sis with certain trees, especially oais. One finds<br />

then in several regions <strong>of</strong> Southern europe. paryicular<br />

ip in France, spain and Itaiy.Presently, truffles are<br />

differentiated by microscopic analysis <strong>of</strong> their spores<br />

Ir! the framework <strong>of</strong> The Truf'fie Project, we developed<br />

a Dynamic Headspace Analysis Method allowing the<br />

direct isolatior <strong>of</strong> volatiles naturally emited from<br />

entire unbrushed fresh truffles. The aroma volatiles<br />

are concentrated on a Tenax CC trap and then thermaliy<br />

desorbed for capillary gas chromatographic analysis.<br />

The gas chromatographic pr<strong>of</strong>iles used as Finger Print<br />

allowed us to rapidly and reliably determine the<br />

species <strong>of</strong> truffles analysed.The methodology was<br />

appiied to the most comniun species cf french truffles.<br />

J.W. TAYLOR, T.D. BRUNS, and T.J. WHITE,<br />

Departments <strong>of</strong> Plant Biology and Plant<br />

Pathology, University <strong>of</strong> California,<br />

Berkeley, CA 94720 and H<strong>of</strong>fmann-La Roche,<br />

Inc., Emeryville, CA 94608<br />

Unusual rate <strong>of</strong> molecular evolution in the<br />

ribosomal DNA internal transcribed spacer <strong>of</strong><br />

Sordariaceae?<br />

DNA sequences <strong>of</strong> rDNA internal transcribed<br />

spacer (ITS) and 5.8s rDNA <strong>of</strong> NeUroSDora<br />

crassa, N. fetras~erma, Sordaria fimicola,<br />

and GelaSln0~~0ra calocera were obtained to<br />

study the phylogenetic relationships <strong>of</strong> these<br />

taxa. Intergeneric ITS nucleotide<br />

substitution was 2-3%, interspecific<br />

nucleotide substitution was 0.5%. This<br />

amount <strong>of</strong> substitution is surprisingly low<br />

compared to amounts <strong>of</strong> substitution in other


Ascomycotina, ~asidiomycotina, and plants, J. A. TRAOL'AIR. Dept. <strong>of</strong> Plant Sciences. Univers~ty <strong>of</strong><br />

e.g., variation among Wccaria (Agaricales) Western Ontario, London, Ontario, Canad2 N6A 5B7.<br />

species is 3-5%. We are examining<br />

explanations for the low amount <strong>of</strong> ITS<br />

nucleotide substitution in Sordariaceae: i!<br />

Mycelial interactions and biosystematics <strong>of</strong> Hirschionorus<br />

unusuallv slow ITS evolution in these funsi,<br />

(Trichaptum) species.<br />

ii ) unus;ally slow evolution throughout their<br />

nuclear DNA or, iii) different generic Interactions in agar culture were studied as a first step in '<br />

concepts in relation to molecular and determining the role <strong>of</strong> mycelial interactions in the<br />

morphological variation in Sordariaceae and<br />

Agaricales. In the first two cases, rates <strong>of</strong> development <strong>of</strong> dark-colored zone lines in wood<br />

nucleotide substitution in mitochondria1 DNA supporting basidiomes <strong>of</strong> Hirschio~orus spp. In addition,<br />

should be similar in all taxa. in the third reactions to controntations with other ~olvnores were<br />

case, rates in mitochondria1 DNA should also<br />

be slower only in Sordariaceae. From the<br />

Sordariaceae, we have amplified a part <strong>of</strong> the<br />

165 mitochondria1 rDNA known to be variable<br />

in Agaricales and are sequencing this DNA to<br />

answer our question.<br />

M.THIBAUT and M.Ah'SEL. Laboratoire de Parasitologie,<br />

I>, rue de 1'Ecole de MCdecine,F 75270 Paris Cedex06<br />

Fungi allergenic towards to humans.<br />

Allergenic manifestations caused by fungi are due to<br />

a great number <strong>of</strong> species, <strong>of</strong>ten different from<br />

these causing mycotic infections. Allergenic fungi<br />

belong principally to " Fungi imperfecti ". They are<br />

found particularly in the atmosphere, which carries<br />

xerospores.<br />

For the study <strong>of</strong> air borne fungus spores, two methods<br />

are used. i - Glvcerine plate method : plates lined<br />

with a coat <strong>of</strong> vaseline or glycerine are exposed for<br />

2L hours on a terrace. They can be colored by the<br />

methyl blue, but spore observation may be made without<br />

preparation under the microscope. We can thus count<br />

large spores. I1 - Cultures <strong>of</strong> colonies on Petri<br />

dishes :this permits the study <strong>of</strong> numerous species.<br />

Starting at a stage <strong>of</strong> sufficient maturation, we<br />

subculture each colony.<br />

The chief genera <strong>of</strong> allergenic fungi encountered in<br />

the atmosphere are the following : Aleurisma,Alterna-<br />

-<br />

.ria, Aspergillus, Botrytis, Chaetomiurn, Cladosporiurr.,<br />

Epicoccun, Fusariurn, Helminthosporium,liomodendrum,<br />

Hucor, Nigrospora, Oospora, Ozonium, Penicillium,<br />

Phoma, Puccinia, Pullularia, Rhizopus, Rnodotorula,<br />

Scopulariopsis, Sepedonium, Stemuhylium, Spondylo -<br />

cladium, Trichodema, Vstilagc:<br />

The two methods answered well as tests <strong>of</strong> the presence<br />

<strong>of</strong> fungi in the atmosphere. A small number <strong>of</strong> fungi<br />

constitute most <strong>of</strong> the mycotic flora. These genera<br />

are the same as those <strong>of</strong> surroundings . There is<br />

considerable interest taken in the subject <strong>of</strong><br />

atmospheric fungi causing allergenic diseases.<br />

4 - a<br />

evaluated as sources <strong>of</strong> taxonomic information on<br />

interrelationships between selected ,Hirschioporus species.<br />

Three dikaryotic isolates <strong>of</strong> each <strong>of</strong> H. parcamenus, H.<br />

subchartaceus, and H. abietinus were paired with each<br />

other and with Trametes hisuida. Cerrena unicolor, Fomes<br />

Dini or Gloeo~hvllum sae~iarium on malt agar in plastic<br />

petri plates and slide cultures. Interspecific confrontations<br />

resulted in distinctive demarcation lines containing<br />

clasping branches plus or minus variously coloredinteraction<br />

zones depending upon the combination.<br />

Reactions included antibiosis, hyphal interference and<br />

mycoparasitism. Different Hirschiovorus species reacted<br />

differently to other polypores but reactions <strong>of</strong> H.<br />

pareamenus and y. subchartaceus were predictably<br />

similar.<br />

- E. r l l o . University <strong>of</strong> Hawaii,<br />

Dept. <strong>of</strong> Plant Pathology, 3190 Maile Way,<br />

Honolulu, HI 96822. Biological control<br />

<strong>of</strong> weeds with fungl plant pathogens. MSA<br />

'90 SYMPOSIUM -- "INDUSTRIAL MYCOLOGY".<br />

All fungal pathogens <strong>of</strong> a weed have poten-<br />

tial as biological controls <strong>of</strong> the species.<br />

To be useful they must be restricted in pa-<br />

thogenicity. Other important attributes <strong>of</strong><br />

successful mycoherbicides are, ability to<br />

grow readily in artificial media, capability<br />

to sporulate in vitro, ability to aerminate<br />

and infect host tissues in less than 24 hrs,<br />

and capability <strong>of</strong> becoming air borne for<br />

ease <strong>of</strong> dispersal. The plant pathogens with<br />

most <strong>of</strong> these attributes but inefficient<br />

dispersal mechanism make economically<br />

valuable bioherbicides. Members <strong>of</strong> Colle-<br />

totrichum, Melanconium, Se~toria, Fusarium,<br />

Acremonium, Phvto~hthora, and Pvthium, make<br />

excellent bioherbicides. Wide pathogenicity<br />

range, lack <strong>of</strong> wind dispersal, or fastidious<br />

cultural characteristics, does not preclude<br />

fungal pathogens from being used as biolo-<br />

gical control agents, but excludes them as<br />

bioherbicides. Obligate parasites are best<br />

suited for classical biocontrol <strong>of</strong> intro-<br />

duced weeds and although they require little<br />

manipulation, their economic value is meas-<br />

urable in their effectiveness in bringing<br />

about ecological balance between introduced<br />

weeds and indigenous floras <strong>of</strong> a particular<br />

region. Pathogens in Puccinia and Fntvloma<br />

are useful biocontrols <strong>of</strong> introduced weeds.


F. A. Wclrer, -tic Botany and -logy<br />

-t=Y, =* -, me*<br />

Beltsville,, MD 20705.<br />

Paraphyses in Phanoesis<br />

Phaoopsis iavanica on AsDarsqus fraa Lndoaesia<br />

(Java) differs fram other P-is in that it<br />

prcducss~paraphyses. Since the disoovery <strong>of</strong> this<br />

distinctive character two other &Utes and a few<br />

herbarim specimens have been fcnuxl that exhibit<br />

it. The morphology, taxoncmy, and g-hic<br />

distribution <strong>of</strong> the paraphysate species are<br />

discussed.<br />

&UARDO M. VADELL, MICHAEL T . HOLMES , AND JAMES C.<br />

CAVENDER. Department <strong>of</strong> Botany, Ohio University,<br />

Athens, OH 45701 - A Natural-Historical Approach to<br />

the Cellular Slime Molds <strong>of</strong> Tikal<br />

rhe Mayan archeological site <strong>of</strong> Tikal (Peten district,<br />

Guatemala; 17.5 North Latitude) <strong>of</strong>fers an unusual<br />

abundance and richness <strong>of</strong> dictyostelids, in agreement<br />

uith the great plant and.anima1 diversity <strong>of</strong> the semi-<br />

evergreen rainforest which surrounds the ruins.<br />

Twenty-five species were isolated from several<br />

soil collections. Four were undescribed species. The<br />

known species were determined using the morpnological<br />

criteria <strong>of</strong> Raper (1984) and Hagiwara (1988). These<br />

conjugated physiological, morphological and behavior-<br />

al criteria include optimal media and temperature for<br />

growth; aggregation pattern; habit and brancning pat-<br />

tern; sorophore base and tip shape; dimensions <strong>of</strong><br />

sori, branches and sorocarps; phototropic response;<br />

chemotaxis to cyclic AW; slug behavior; and spore<br />

size, shape, color and morphology.<br />

The ecological conditions <strong>of</strong> the Tikal forest<br />

region such as alternative wet and dry seasons allov<br />

some insight into the evolution <strong>of</strong> dictyostelids.<br />

For example, the seasonal variation <strong>of</strong> species may<br />

provide clues to the polarity <strong>of</strong> characteristics<br />

which have been selected over time.<br />

One <strong>of</strong> the species isolated is probably an ances-<br />

tral Dictvostelium discoideum. This isolate will pro-<br />

vide an opportunity for studying adaptative strategies<br />

and evolution <strong>of</strong> this species.<br />

C. GERALD VAN DYKE and CHARLES W. MIMS,<br />

Department <strong>of</strong> Botany, North Carolina State<br />

University, Box 7612, Raleigh, NC 27695, and<br />

Department <strong>of</strong> Plant Pathology, University <strong>of</strong><br />

Georgia, Athens, 30602. Light and electron micro-<br />

scopy <strong>of</strong> conidium germination and appressorium<br />

development in Colletotrichum truncatum.<br />

Colletotrichum truncatum has been used for bio-<br />

control <strong>of</strong> the weed 5esbianiaexaltata. Light and<br />

electron microscopic techniques were used to<br />

study events occurring during conidium germ-<br />

ination and appressorium formation. Events were<br />

observed at 22 C up to 12 hrs after conidia were<br />

placed on host tissue and artificial membranes.<br />

Ndclear division occurred 1-2 hrs after place-<br />

men;, followed 5!. formation <strong>of</strong> a central conidial<br />

septum. A germ tube (GT) emerged 2-3 hrs later;<br />

the nucleus <strong>of</strong> the germinated conidial cell<br />

divided, one nucleus remained in the conidium, the<br />

other migrated into the GT. A swollen, terminal<br />

appressorium formed 2-3 hrs later; the GT<br />

nucleus divided in the appressorium, now de-<br />

limited from the GT by a septum. An extracellular<br />

matrix coated conidia, GTs, and appressoria and<br />

appeared to stick fungal structures to host tissue<br />

and membranes. Infection pegs formed from<br />

appressoria 9-1 2 hrs after germination.<br />

---<br />

E. VAN EECKHOUT., I. BLACKWELL, and H.C. RUSH. Depsrtment <strong>of</strong><br />

Botany and Depsrtmt <strong>of</strong> Plant Pathology and Crop Physiology,<br />

Louisiana State University, Baton Rouge. LA 70603.<br />

In vitro effects <strong>of</strong> propicanazole on morphology and ultrastructure<br />

<strong>of</strong> Rhizocton~a solani.<br />

--<br />

Rhizoctonia solani Kbn (AG1) is the causal agent <strong>of</strong> rice sheath<br />

blight, the mst inportant rice disease in the southern riceproducing<br />

areas <strong>of</strong> the United States. Propiconazole, a sterol<br />

synthesis inhibitor. is one <strong>of</strong> the fungicides currently registered<br />

for use in cmtrolling this disease. Agar incorporation <strong>of</strong><br />

propiconatole shod good in vitro activity against R. solani. EC<br />

50 values ranged from 0.1 to 0.3 ppn depending on tim after<br />

irwcuiatia. Colony growth uas conpletely inhibited at 10 ppn.<br />

Exposure <strong>of</strong> R. solani to propiconazole induced rhythmic growth in<br />

culture which can be related to the node <strong>of</strong> action <strong>of</strong><br />

propiconazole. Control and propiconatole treated hyphse were<br />

premred for scanning and transmission electron microscopy.<br />

Morphological changes in response to fungicidal activity included<br />

(a) irregular branching uith decreased intervals between branches.<br />

(b) short, stubby branches, (c) abnormal thickenings and<br />

constrictions, end (d) ruotures in usually inflated hyphal parts.<br />

Electron microsco~ic examination <strong>of</strong> freeze-substituted and<br />

chemically fix- hyphal tip sections revealed disrupted apical<br />

vesicle configuraticns and abnormal wall inclusions as most<br />

obvious effects <strong>of</strong> propiconazole on ultrastructure <strong>of</strong> R. solani .<br />

Rytas Vilgalys. Department <strong>of</strong> Botany, Duke University,<br />

Durham, NC 27706.<br />

The application <strong>of</strong> genetic data tor interpretive<br />

mycogeography.<br />

As more becomes known about diverse geographic<br />

distributions <strong>of</strong> fungi, new sources <strong>of</strong> independent data will<br />

be necessary to evaluate competing histor~cal hypotheses.<br />

Evidence from macromolecular data should benefit studies<br />

on interpretive mycogeography for several reasons: 1)<br />

Molecular data represent an unlimited source <strong>of</strong> characters<br />

for phylogenetic analysis at almost any taxonomic level; 2)<br />

Different modes <strong>of</strong> inheritance and recombination in nuclear<br />

and mitochondria1 genomes provide two alternative sources<br />

<strong>of</strong> information; 3) Recent technical advances in molecular<br />

biology now make DNA-level analyses possible with minute<br />

tissue samples from natural material. I will discuss the<br />

application <strong>of</strong> data for examining vicariance biogeography in<br />

macr<strong>of</strong>ungi. The relatively high rate <strong>of</strong> genome evolution in<br />

many members <strong>of</strong> the Basidiomycotina should also make it<br />

possible to examine intraspecific phylogeography and its<br />

relation to gene flow, genetic divergence and speciation.


Michael 4. Vincent. Department <strong>of</strong> Botany,<br />

Miami University, Oxford, OH 45056.<br />

Notes on Hyphomycetes from the Bahamas.<br />

Recent field work on Andros and San<br />

Salvador islands in the Bahamas has added<br />

significantly to the known fungal flora <strong>of</strong><br />

the archipelago. Nearly 175 taxa new to<br />

the Bahamas have been identified from two<br />

excursions to the islands, including many<br />

hyphornycetes. Several new species have<br />

been discovered, as well as a new<br />

basidiomycetous ananlorph genus. Among the<br />

genera collected are Acremonium,<br />

I D O ~ ~ W ,<br />

Dendrv~hi-, D-,<br />

Ewicocc!m ! Fusarium, L+!xlU+l<br />

Le~toxvwhlum Mvrotheclum, NlarosDora !<br />

Nodu~~oriUlI, paecilomvces , P-,<br />

Periconig, Pestalotia, P-, . .<br />

P' I S bo<br />

s:;X;EZ T a % . ; . e g. f ; o F 1<br />

Trichodermp, y e r t l c u and ZvaosworiUm.<br />

In addition, several fungi have been<br />

cultured which have thus far eluded<br />

identification. The species <strong>of</strong> the genera<br />

listed will be discussed, and the new taxa<br />

will be described.<br />

H. S. VISHNIAC and 0. T. JOHNSON. Dept <strong>of</strong> Botany and<br />

o iogy, Oklahoma State U, Stillwater OK 74078<br />

and Dept. <strong>of</strong> Entomology, U. Arkansas, Fayetteville AR<br />

72701.<br />

Trichosporon cutaneum mediates aggregation by a<br />

frugivorous beetle.<br />

The adult green June beetle (Cotinis nitida) aggregates<br />

on fruit when attracted byrfeeding beetles.<br />

Field experiments by Domek and Johnson established<br />

that aggregation was induced by semiochemicals and<br />

that fungistatic agents inhibited aggregation. The<br />

course <strong>of</strong> development <strong>of</strong> a yeast flora in adult<br />

beetles is: beetles emerging from pupation have no<br />

yeast flore; a smalllargely fermentative flora is<br />

acquired from soil and fruit; with increased feeding<br />

(by 1 aboratory-reared beetles on peach slices )the<br />

yeast flora increases in population density and<br />

becomes 1 argely (60%) non-f ermentati ve. Most drarnatically,<br />

Trichosporon cutaneum biovarswere observed<br />

to rise f m<br />

<strong>of</strong> the gut flora and from 1%<br />

to 53% <strong>of</strong> yeasts on food-substrate. In field trials,<br />

peach slices inoculated with Tr. cutaneum were no<br />

more attractive than slices iGcu1 ated with ferment-<br />

ative yeasts, but when laboratory-reared beetles fed<br />

on such slices were included in the bait, such baits<br />

were as attractive as wild beetles with natural<br />

micr<strong>of</strong>lora. Trichosporon cutaneum was both necessary<br />

and sufficient for semiochernical production by adult<br />

green June beetles feeding on fruit.<br />

THOMAS J. VOLK Department <strong>of</strong> Botany, UW-<br />

Madison Madison WI 53706 and Forest Products<br />

Laboratory, Center for Forest Mycology Research One<br />

Gifford Pinchot Dr. Madison WI 53705 and THOMAS<br />

J. LEONARD Departments <strong>of</strong> Botany and Genetics UW-<br />

Madison Madison WI 53706.<br />

Heterokaryon formation between monoascosporous<br />

strains <strong>of</strong> Morchella.<br />

Three lines <strong>of</strong> evidence are reponed for heterokaryon<br />

foxmation in Morchclla esculcnta and related species.<br />

Cultural studies demonstrated a genetic basis for<br />

different types <strong>of</strong> interactions between mycelia from<br />

sister and non-sister spores. Cytological studies <strong>of</strong> the<br />

mycelial interaction between non-sister monoascosporous<br />

isolates,demonstrated nuclear pairing in presumptive<br />

heterokaryons. Two different mutations isolated in this<br />

study were used to show genetic complementation in<br />

these heterokaryons.<br />

THOMAS J. VOLK Deparmlent <strong>of</strong> Botany, UW-<br />

Madison Madison WI 53706 and Forest Products<br />

Laboratory. Center for Forest Mycology Research One<br />

Gifford Pinchot Dr. Madison WI 53705 and THOMAS J.<br />

LEONARD Depanments <strong>of</strong> Botany and Genetics UW-<br />

Madison Madison WI 53706.<br />

Cytological studies <strong>of</strong> the life cycle <strong>of</strong> Morcl~ella.<br />

Various stages <strong>of</strong> the morel life cycle were<br />

studied cytologically. Photomicropaphic evidence<br />

demonsaa~es that the average number <strong>of</strong> nuclei per<br />

cellular compartment in vegetative hyphae <strong>of</strong> Morchella<br />

is 10-15 and that hyphal fusions are auiie frequent. The<br />

resting structures, the scleroda, are actus!iy<br />

pseudosclerotia which form from the re!!cated branching<br />

and enlargement <strong>of</strong> terminal hyphae from either primary<br />

(homokaryotic) or secondary (heterokayoticj kyphae.<br />

Photomicrographs also depict the develop men^ <strong>of</strong> fruiting<br />

body primordia. Photomicrographs <strong>of</strong> ascus develop men^<br />

demonstrates autogamy rather than de novo heterokaryon<br />

formation by hyphal fusion in the subhymenial layer <strong>of</strong><br />

the fruiting body. For the first time a comprehensive life<br />

cycle diagram <strong>of</strong> the morel is introduced.<br />

R. E. WAGNER. H.M. SHIN and H.T. WILKIKSON,<br />

Dept. <strong>of</strong> Piant Pathology, University <strong>of</strong> Illinois<br />

at Urbana-Champaign, 1102 S. Goodwin Ave.,<br />

Urbana, IL 61801.<br />

Spheroplast formation from cysts <strong>of</strong> Phytophthora<br />

megaspema £.SF. glycinea.<br />

High yields <strong>of</strong> spheroplasts were produced when<br />

cysts <strong>of</strong> Phptophthora megasperma f.sp. glycinea<br />

were incubated in 0.01 M dithiothreitol for 40 min<br />

followed by incubation in 0.6M sorbitol dissolved<br />

in citric acid buffer (pH 5.6) containing the<br />

digestive enzymes Meiceiase (celiulase), Rhozyme


(hemicellulase), and Novozym 234 (glucanase,<br />

xylanase, lamarinase and chitinase) for 8 hr at<br />

30 C. Meicelase and Rhozyme were added at 10 mg/ml.<br />

Novozym was added at 0.0'2 mg/1000 cysts. Cysts<br />

lysed when incubated at higher concentrations <strong>of</strong><br />

Novozym 234. Cysts germinated. many bipolarly,<br />

following treatment with the enzymes when sorbitol<br />

concentrations were less than 0.5 M. The addition<br />

<strong>of</strong> magnesium sulfate (0.1 M) to the-incubation<br />

medium produced highly stable spheroplasts even<br />

at high levels <strong>of</strong> Novozym 234 (2.0 mg/1000 cysts).<br />

Spliuroplast size increased as the concentratioz<br />

<strong>of</strong> magnesium sulfate was increased (0.01 M-0.5 M).<br />

Protoplasts were liberated from spheroplasts when<br />

the osmotic potential <strong>of</strong> the sorbitol incubation<br />

medium was reduced from 0.6 M to 0.4 M. Proto-<br />

plasts lysed within 10 min <strong>of</strong> emergence.<br />

5 S. WFINBAUM. M.F. ALLEN, C.F. FRIESE and E.B. ALLEN. Dept<br />

<strong>of</strong> Biology, Systems Embgy Research Group, San Diego State<br />

University, San Diego CA 921 82-0057.<br />

Observations <strong>of</strong> the interface between VAM fungi and rnycotrophic<br />

versus nonmycotrophic plants.<br />

We previously reported that invasion by VAM tungi <strong>of</strong> the<br />

nonmycotrophic plant Salsola resulted in aut<strong>of</strong>luorescing and<br />

a rapid browning <strong>of</strong> the root tissue which was not observed in the<br />

rnycotrophic grass -. This could result in<br />

the death <strong>of</strong> the nonmycotrophic seedlings. We extended these<br />

observations to other nonmycotrophic and mycotrophic plants.<br />

Four different responses to the fungi were observed. In annual<br />

Chenopodiaceae. and -, aut<strong>of</strong>luorescence and<br />

rapid (within a day) browning was observed. W d i u m album<br />

and w n alomeratus showed browning with faint<br />

aut<strong>of</strong>luorescence.<br />

, B. and .mh&Qsh<br />

thaliana had no reaction and no root penetration by the VAM tungi.<br />

The grasses showed no browning or aut<strong>of</strong>luorescence but tormed<br />

normal VAM. The shrub<br />

.. . had normal VAM but<br />

as the tissue aged, it began to aut<strong>of</strong>luoresce and turn brown. No<br />

subsequent infection <strong>of</strong> these mot segments was observed. We<br />

suaoested that these 4 types <strong>of</strong> responses relate to the ability <strong>of</strong><br />

thehost to reject or form a VA rnycorrhizal association.<br />

M. C. WILLIAMS and R.D. GRIGG. Department <strong>of</strong> Biology.<br />

Kearney State College, Kearney, NE 68849<br />

A preliminary report on host specificity <strong>of</strong> selected<br />

Smittium z. (Trichomycetes) isolates.<br />

Species <strong>of</strong> the Trichomycete genus Smittium Poisson<br />

have been isolated from dipteran larvae including<br />

Chironomidae, Culicidae, Simuliidae and Tipulidae.<br />

Limited studies have shown that some Smittium spp.<br />

isolates are able to infest a "foreign" mosquito<br />

(Culicidae) host. For this study selected Smittium<br />

isolates. which were not available at the time <strong>of</strong><br />

the earlier study, were grown in shake culture and<br />

the trichospores separated by filtering. The spores<br />

were fed to mosquito and blackfly (Simuliidae) larvae<br />

which were later dissected and examined for the<br />

presence <strong>of</strong> the Smittium isolate. The results<br />

support the hypothesis that some Smittium species<br />

tend to have a restrictecl host range while others<br />

may infest differen: :nsect host families.<br />

Wolfe, C. B., Jr. Biology Department, Penn State<br />

University, Mont Alto, PA 17237. The Penn State<br />

University <strong>Mycological</strong> Herbarium (PACMA).<br />

The <strong>Mycological</strong> Herbarium <strong>of</strong> Penn State ' 'v was<br />

recently moved from the University Part . to the<br />

Mont Alto Campus, and a new curator v .~ted. The<br />

herbarium has a lengthy and ,. It houses<br />

approximately 67,500 specimens thr ,resentative <strong>of</strong><br />

, mostly from the<br />

~lections are from<br />

other locations around the<br />

.andle (Ustilaginales), and<br />

reputation was established<br />

. a prolific collector, and the<br />

,adth <strong>of</strong> his interests. Included<br />

, are approximately 150 type<br />

specimens (b. J-, iso-, syn-, and paratypes). Several<br />

exsiccati a- med by the herbarium including 4900<br />

specimev ~vlycotheca Marchica issued by P. Sydow<br />

many b. are types. The herbarium has historically<br />

been undc .tilized due, perhaps, to a lack <strong>of</strong> awareness <strong>of</strong><br />

the diversity <strong>of</strong> its collections and also a fairly restrictive<br />

loan policy. With the move <strong>of</strong> the herbarium and<br />

appointment <strong>of</strong> a new curator, a more reasonable loan<br />

policy is now in effect, and researchers are encouraged to<br />

request loans <strong>of</strong> materials that the herbarium might hold.<br />

C. G. Wu and J. W. Kimbrough, Plant Pathology Dept.,<br />

Cniversity <strong>of</strong> Florida, Gainesville, FL., 32611.<br />

Comparative Ultrastructure <strong>of</strong> Spore Ontogeny in the<br />

Humariaceae (Pezizales).<br />

Very little research has been done on the ultrastruc-<br />

ture <strong>of</strong> spore ontogeny in members <strong>of</strong> the Humariaceae<br />

(=Pyronemataceae, Otideaceae, or Aleuriaceae by some),.<br />

The purpose <strong>of</strong> this poster is to describe the fine<br />

structure <strong>of</strong> spore ontogeny in Aleuria, Cheilvmenia,<br />

Otidea, Tarzetta, and Trichophae;.<br />

--<br />

In all genera except Tarzetta, an electron-translu-<br />

cent primary wall layer is deposited between the two<br />

spore delimiting membranes. k narrow, electron-opaque<br />

band, the epispore, is deposited onto the primary<br />

wall. In Aleuria and Cheilymenia this coincides with<br />

an expansion <strong>of</strong> outer delimiting membranes to form a<br />

perisporic sac. The perisporic sac develops later in<br />

--<br />

Otidea, Tarzetta, and Trichophaea. A slightly opaque,<br />

granular matrix develops within the perisporic sac<br />

and later condenses into granular particles which<br />

overlays the epispore to form the secondary wall.<br />

Secondary walls <strong>of</strong> the species studied differ in fibrillar<br />

structure and staining properties.<br />

Spore ontogeny in Tarzetta was peculiar in that the<br />

initial wall is a narrow, slightly opaque band onto<br />

which fragments <strong>of</strong> the epispore are deposited. These<br />

fragments coalesce into a solid dark band. An additional<br />

electron-transparent primary wall forms between<br />

the dark band and the sporoplasm. In Cheilymenia<br />

a transparent band also forms between the epispore<br />

and secondary wall, and later the secondary wall may<br />

become detached from the epispore to form a spore<br />

sheath.


C. G. Wu and J. W. Kimbrou~h. Plant Pathology Dept.,<br />

University <strong>of</strong> Florida, Gainesville, FL.. 32611.<br />

Septal Ultrastructure in Selected genera <strong>of</strong> Humariac-<br />

eae (Pezizales).<br />

Septal structures have been found to be very consist-<br />

ent at the generic and family levels in well defined<br />

families <strong>of</strong> operculate Discomycetes. This has not been<br />

true <strong>of</strong> the large and heterogenous family Humariaceae<br />

(=Pyronemataceae, Otideaceae, or Aleuriaceae by some).<br />

The fine structure <strong>of</strong> septa in asci, ascogenous hyphae,<br />

paraphyses, . .. and excipular cells were studied in the<br />

following genera: Aleuria, Clreilymenia, Mycolachnea,<br />

Otidea, Scutellinia, and Trichophaea.<br />

Septal pore plugs in ascal bases are shaped initially<br />

by the configuration <strong>of</strong> membrane structures in the<br />

vicinity <strong>of</strong> the pore. All ascal pore plugs begin as<br />

a hemispherical, granular matrix onto which electron-<br />

opaque zones <strong>of</strong> additional granules are deposited.<br />

Those <strong>of</strong> Aleuria and Trichophaea have laminated,<br />

transparant zones bordering the pore and little or no<br />

granular matrix is left in the subtending ascogenous<br />

hyphal cell. This type <strong>of</strong> ascal pore structure is<br />

referred to as the "aleurioid" type. A somewhat simi-<br />

lar pore structure is found in asci <strong>of</strong> the remaining<br />

genera, although without the laminated, translucent<br />

bands. The latter are remarkedly similar to those<br />

found in members <strong>of</strong> the Ascobolaceae.<br />

Septal pores <strong>of</strong> paraphyses and excipular cells are<br />

generally the same, where the pore is spanned by a<br />

finely striated matrix <strong>of</strong> granular material attached<br />

to the border <strong>of</strong> the pore. The size and shape <strong>of</strong> this<br />

matrix differs slightly in each genus. Unilike pores<br />

<strong>of</strong> asci and ascogenous hyphae, Woronin bodies are con-<br />

spicuous around -the -pores <strong>of</strong> vegetative-cells .<br />

MEI-LEE WU and R. T. HANLIN. Department <strong>of</strong> Plant<br />

Pathology, University <strong>of</strong> Georgia, Athens, GA 30602.<br />

Ascomal development in Leptosphaerulina crassiasca.<br />

Leptosphaerulina crassiasca was isolated from peanut<br />

leaves with symptoms <strong>of</strong> pepper spot disease. Cultures<br />

from single ascospores formed ascomata, indicating<br />

that the fungus is homothallic. Ascospores germinated<br />

readily on agar, forming septate hyphae with<br />

uninucleate cells. Fertile hyphae soon form on the<br />

mycelium; these are larger and usually have binucleate.<br />

cells. The cells <strong>of</strong> the fertile hyphae divide<br />

repeatedly to form ascostromal initials. As the<br />

ascostromata enlarge, small binucleate ascogenous<br />

cells with dense cytoplasm are differentiated near the<br />

center. Karyogamy occurs, forming the young asci;<br />

these expand, filling the center <strong>of</strong> the ascostroma.<br />

No sterile centrm tissues are formed. Meiosis and a<br />

single mitotic division result in 8 nuclei which are<br />

delimited into ascospore initials. Further divisions<br />

form the mature multinucleate dictyospores. The ascus<br />

wall is two-layered, with the inner layer extending<br />

during ascospore discharge. As the asci form, the<br />

outermost cells <strong>of</strong> the ascostroma become pigmented and<br />

thick-walled, and a papillate ostiolar neck forms at<br />

the apex. The ascoma is a uniloculate pseudothecium<br />

with bitunicate asci. Ascomal ontogeny is typical <strong>of</strong><br />

the Dothidea-type <strong>of</strong> development. On V-8 agar mature<br />

pseudothecia form in 6 days, making this a good<br />

Loculoascomycete for class use.<br />

QIUXIN WU, Department <strong>of</strong> Botany, The<br />

Universlty <strong>of</strong> Tennessee, Knoxvllle, TL 37996-<br />

1100. Intercompatlblllty studles wlth<br />

Clavicorona ovxldate<br />

Clavicorona uvridata is distributed across<br />

The North Temperate Zone and exhibits<br />

conslderable basldlocarp morphological<br />

variation. Self-crosses <strong>of</strong> monokaryotlc<br />

lslnqle-basldlospore) Isolates shov that the<br />

specles 1s blfactorally Incompatible.<br />

Intercollectlon matlngs among North Amerlcan<br />

stralns and also cross-continent matlngs show<br />

that the morphospecles is congruent vlth the<br />

bloloqlcal species.<br />

DANIEL A. WUBAH~, M. S. NLLER~ and D. E AKIN~.<br />

l~otan~ Dept.. University <strong>of</strong> Gcorgia. Athens, GA 30602 and<br />

'plant Structure and Composition Unit, Russell Res. Cu,<br />

USDNARS Athens, GA 30616<br />

Caecomyccs (= Sphamnno~s sensu Orpin) is one <strong>of</strong> the four<br />

described genera <strong>of</strong> obligately anaerobic zoosporic fungi. Fungi in<br />

this genus form a monocentric thallus which develops endogenously<br />

with the nucleus remaining in the zoospore cyst and multiplying<br />

there. The cyst may enlarge into an incipient sporangium. In<br />

addition to this basic developmental pattern . we have observed that<br />

an isolate <strong>of</strong> Caccomyces, obtained from cow feces, fonns a<br />

multisporangiate thallus with the sporangia atrached to a vegetative<br />

cell which functions in a manner similar to the prosporangium<br />

described for Calt?noct!vfridium sp. We also observed a shift from<br />

the formation <strong>of</strong> monocentric thalli to the produaion <strong>of</strong> polyoentric<br />

thalli. This unusual development <strong>of</strong> Cacwmyces wil be discussed<br />

and compared to exogenousendogenous development in some<br />

aerobic Chytridiomycetes.<br />

J.C. Zak and D. Freckman, Ecology Group, Dept. Biol.<br />

Sci., Texas Tech University, Lubbock, TX, 79409, &<br />

Dept. Nematol., U.C. Riverside, Riverside, CA., 92521.<br />

Root region interactions: effects <strong>of</strong> micr<strong>of</strong>aunal<br />

grazing on fungal assemblages <strong>of</strong> a desert bunchgrass.<br />

The root region represents a major center <strong>of</strong> micro-<br />

floral-micr<strong>of</strong>aunal activity in desert ecosystems.<br />

The effects <strong>of</strong> micr<strong>of</strong>aunal grazing in the root<br />

region <strong>of</strong> Erioneuron pulchellum on the species compo-<br />

sition and organization <strong>of</strong> the root surface fungal<br />

assemblage was followed over a two year period.<br />

Microarthropod and nematode densities were decreased<br />

by the periodic application <strong>of</strong> either chlordane or<br />

nemocur. While micr<strong>of</strong>aunal densities changed, the<br />

number <strong>of</strong> fungal species associated with the root<br />

surface was not altered. Changes in species composi-<br />

tion <strong>of</strong> the fungal assemblages were observed follow-<br />

ing treatment indicating that altered grazing pres-<br />

sure resulted in compensatory changes. Rhizosphere<br />

hyphal lengths also did not differ among treatments<br />

for either year. Trophic relationships rather than<br />

micr<strong>of</strong>aunal densities in the root region may regulate<br />

nitrogen dynamics and plant growth.


--- Mujeeb i!. k'beri -- - , Faculty <strong>of</strong> Forestry, Ur.iversity <strong>of</strong><br />

Toronto,l'oronto. Octario Y5S ;A1 , Canada.<br />

9lo~esticide.s.<br />

During a recent investigation <strong>of</strong> microor,-anisms<br />

associated with the eastern subierranean termite<br />

&eJiculitermes fi&gsl~ollar), (Zoberl & Grace<br />

1990c,%n;e-o,' the fungal associates isolated were<br />

found suitable for the biolo6:ical control <strong>of</strong> termites<br />

These isolates, Gong with some entomopathogenic<br />

fungi (obtained frorr. the Biosystema~icsResearch<br />

Centre, 0ttawa) were investii;ated. To ascertain their<br />

ecological competence, some ex~eriments were<br />

performed. to observe iht f llri~bi-f~~i6~: interactio?.~<br />

upor, f =gal- te-nite interactions. rhe most suitabie<br />

strains were selected, the criteria for selection<br />

were: A. Mortality <strong>of</strong> termites within a relatively<br />

shorter period after inoculation 9. Growth and<br />

sporulation <strong>of</strong> the funeus on simple culture media at<br />

a wider range <strong>of</strong> temperatures C. Viability <strong>of</strong> the<br />

fungus for a relatively longer period D. Ecological<br />

competence.<br />

-- Beauveria bassiana (~alsamo) %as found suitable for<br />

termite control, the most suitable strain <strong>of</strong> 5.<br />

bassiana was found to be the one isolated from -<br />

R. flavipes workers infesting a tree in Toronto, it<br />

showd cpmplete dominarce over other microor~anisms<br />

associated with the termites an& sporulated freely<br />

on the dead termites.<br />

Additional Authors<br />

G. C. Adarns (see R. S. Surve)<br />

D. E. Akin (see Daniel A. Wubah)<br />

J. N. Albert (see A. E. Libem)<br />

A. Al-hi (see S. K. AWullah)<br />

E. B. Allen (see M. F. Allen)<br />

(see B. S. Weinbaum)<br />

M. F. Allen (see B. S. Weinbaum)<br />

.A. H. Al-Sacloon (see S. K. Abdullah)<br />

J. F. Ammirati (see S. 0. Rogers)<br />

Z. Q. An (see Myra ChuChou)<br />

(see J. W. Hendrix)<br />

C. Anderson (see S. S. Dhillion)<br />

J. B. And- (see M. L. Smith)<br />

(see R. W. Kenigan)<br />

(see L. M. Kohn)<br />

R. C. Anderson (see B. A. Haney)<br />

(see Hae-Ae Seo)<br />

(see J. Meredith)<br />

M. Ansel (see M. Thibaut)<br />

H. J. AmoU (see H. W. Keller)<br />

A. K. Awasthi (see A. C. Shukla)<br />

M. T. Banik (see H. H. Burdsall, Jr.)<br />

M. Bartolara (see C. A. Shearer)<br />

J. W.BenneU(see J. W)<br />

W. Black (see C. Bradley)<br />

M. Blackwen (see E Van %bout)<br />

W. H. Blackwell (see M. J. Powell)<br />

J. M. Bland (see M. A. Klic';)<br />

C. Bledsoe (see S. 0. Rogers)<br />

M. E. Boraas (see D. Bermudes)<br />

S. M. Boyle (see C. Gruhn)<br />

H. E. Brockman (see L. A. O'Go~nan)<br />

S. Brown (see R. Pinnetk)<br />

J. N. Bruhn (see D. L. Richter)<br />

J. Buchko (see A. Belkhiri)<br />

H. H. Burdsall, Jr. (see M. T. Banik)<br />

(see T. W. Darmono)<br />

(see T. W. Darmono)<br />

-<br />

(see T. mnn)<br />

R. R. Burgess (see T. K. Kirk)<br />

T. D. Burns (see J. W. Taylor)<br />

C. S. Carlton (see A. E. Liberta)<br />

Cassar, S. C. (see R. A. Roeper)<br />

L. A. Castlebury (see R. V. Gessner)<br />

J. C. Cavender (see E. M. Vadell)<br />

(see M. T. Holmes)<br />

C. E. Cerniglia (see J. B. Sutherland)<br />

C. Chakrkook (see J. F. Leslie)<br />

T. E. Chase (see \h'. J. -a)<br />

Y. Chen (see M. S. Manocha)<br />

M. Christensen (see P. D. Srshl)<br />

F. W. Cobb, Jr. (see W. J. Otmsina)<br />

(see T. E. Chase)<br />

J. C. Cooke (see G. E. Madole)<br />

C. B. Cordell (see D. H. Man)<br />

P. J. Cotty (see P. Bayman)<br />

S. F. Covert (see D. Cullen)<br />

J. Davey (see J. Lifrak)<br />

M. Deb (see T. Talou)<br />

P. Diederich (see R. bum)<br />

J. C. Doubli (see D. J. McLaughlin)<br />

G. a-Sayed (see R. GtIpta)<br />

(see T. D. Leathers)<br />

R. Fogel (see 0. K. Miller)<br />

D. Freckman (see J. C. Zak)<br />

J. P. Freeman (see J. B. Sutherland)<br />

C. F. Friese (see M. F. AUen)<br />

(see B. S. Weinbaum)<br />

P. P. Fu (see J. B. Sutherland)<br />

.M. S. Fuller (see D. A. Wubah)<br />

J. R. Garcia (see K. Foss)<br />

A. Gaset (see T. Talou)<br />

L. Giam (see M. M. Stankis)<br />

J. A. Glaser (see R. T. Lamar)<br />

D. A. Giawe (see J. T. Ellzey)<br />

S. A. Gordon (see T. J. Bamni)<br />

R. D. Grigg (seeM. C. Witliams)<br />

J. H. Grove (see J. W. Hendrix)


C. Gruhn (see J. G. Palmer)<br />

R. Gupta (see L. A. O'Gorma.)<br />

J. Haines (see 0. K. Miller)<br />

A. E. Hajek (see D. W. Roberts)<br />

T. M. Had (see M. L. Canverse)<br />

J. Han (see L. A. O'Gorman)<br />

R. T. Hanh (see M. L. Wu)<br />

G. E. Hannan (see C. K. Hayes)<br />

I. B. Heath (see S. G. W. Kaminskyj)<br />

J. W. Hendrix (see Z. Q. An)<br />

(see M. Chu-Chou)<br />

G. T. Henson (see Z. Q. An)<br />

(5% J. W. Hmdrix)<br />

D. E. Hershman (see Z. Q. An)<br />

(see J. W. Hmdrix)<br />

T. L. Highley (see S. C. Croan)<br />

H. C. Hoch (see T. W. Hill)<br />

M. T. Holmes (see E. M. Vadell)<br />

P. A. Horgen (see J. C. Royer)<br />

(see R. W. Kmigan)<br />

(see W. E. Hintr)<br />

J. Hoskins (see P. L. Skamd)<br />

M. Hubbes (see W. E. Hintz)<br />

M. E. S. Hudspeth (see S. A. Ciary)<br />

C. lgn<strong>of</strong>fo (see R. Gupta)<br />

(see T. D. Leathas)<br />

R. K. Jayaswal (see R. Gupta)<br />

X. Jin (see C. K. Hayes)<br />

A. R. Johnson (see K. A. Kuehn)<br />

D. T. Johnson (see H. S. Vishniac)<br />

R. K. Jones (see L. F. Grand)<br />

J. Kaur (see A. C. Shukla)<br />

B. Kearns (see C. Bradley)<br />

J.W. Kimbrough (see C. W. Mims)<br />

(see E. A. Momol)<br />

(see C. G. Wu)<br />

(see C. G. Wu)<br />

T. K. Kirk (see R. T. Lamar)<br />

H. C. Kistler (see E. A. Momol)<br />

G. R. IUassen (see A. Belkhiri)<br />

C. J. R. Klittich (see J. F. Leslie)<br />

K. L. Klomparens (see K. J. Czymmek)<br />

R. D. Koehn (see K. A. Kuehn)<br />

(see M. K. Oakley)<br />

R Koide (see J. Lewis)<br />

J. W. Koning, Jr. (see T. K. Kirk)<br />

K. Korhonen (see W. J. Otmsh)<br />

M. J. Larsen (see M. T. Banik)<br />

A. R. Lax (see M. A. Klich)<br />

T. D. Leathers (see R. Gupta)<br />

S. B. Lehrer (see W. E. Homer)<br />

D. E. Lemke (see M. K. Oakley)<br />

T. J. Leonard (see K. K. Klein)<br />

A. E. Liberta (see B. A. Haney)<br />

(see R. C. Anderson)<br />

A. E. Linkins ID (see R. K. Antibus)<br />

H. Lu (see D. J. Mdaughh)<br />

L. A. L uck (see R. Gupta)<br />

S. Lupo (see L. Bettucci)<br />

J. D. MacDonald (see K A. Jacobs)<br />

B. Maglsanik (see P. L. Miaehart)<br />

D. Mdoch (see M. Blackwell)<br />

S. B. Maul (see D. H. Marx)<br />

D. J. McLaughlin (see E. W. A. Boehm)<br />

(see J. C. Doublks)<br />

R. D. MiIhoIiand (see L. F. Grand)<br />

D. W. Miller (see J. B. Sutherland)<br />

0. K. Miller, Jr. (see T. Flynn)<br />

(see K. U. Jacobson)<br />

(see J. G. Pahner)<br />

C. W. Mims (see T. C. Sewan)<br />

(see C. G. Van Dyke)<br />

C. J. Mirocha (see J. W. McCain)<br />

P. Moutoglis (see M. Cooke)<br />

G. Muener (see 0. K. Miller)<br />

K. H. Nealson (see D. Bermudes)<br />

C. Near (see C. Bradley)<br />

R. T. Nelson (see B. J. Cochrane)<br />

C. P. Novotny (see M. M. Stankis)


M. Oakley (see R. Koehn)<br />

D. J. O'Kane (see W. L. Lingle)<br />

W. J. otrosina (see T. E. Chase)<br />

D. Pfm (see 0. K. Miller)<br />

J. D. Polishook (see G. F. Bii)<br />

D. Pwter (see W. L. Lingle)<br />

P. J. Pukkila (see G. May)<br />

S. W. Queener (see P. L. Skatrud)<br />

K. F. Raffa (see K. D. Klepzig)<br />

C. A. Raper (see J. S. Horton)<br />

W. J. Rea (see K. A. Kuehn)<br />

S. A. Rehner (see S. 0. Rogers)<br />

D. Reynolds (see 0. K. Miller)<br />

E. A. Richardson (see C. W. Mims)<br />

J. K. Roberts (see K. M. T. Cason)<br />

E. W. Robins (see L. A. O'Gorman)<br />

S. 0. Rogers (see K. F. Lobuglio)<br />

A. Y. Rossrnan (see S. C. Redlin)<br />

J. C. Royer (see W. E. Hin~)<br />

R. C. Ruaboro (see D. E. Hemmes)<br />

M. C. Rush (see E. Van Eeckhout)<br />

G. Saem (see M. Berbee)<br />

K. A. Seifert (see G. J. Samuels)<br />

A. L. Selby (see J. B. Sutherlandj<br />

H. M. Shin (see R. E. Wagner)<br />

L. M. Shule (see M. F. Allen)<br />

M. R. Siege1 (see M. Chu-Chou)<br />

D. B. Sinsabaugh (see R. K. Antibus)<br />

(see R. K. Antibus)<br />

E. B. Smalley (see R. H. Proctor)<br />

(see K. D. Klepzig)<br />

K. M. Snetselaar (see C. W. Mims)<br />

J. W. Spatafora (see M. Blackwell)<br />

C. A. Specht (see M. M. Stankis)<br />

P. T. Spieth (see T. E. Chase)<br />

M. R. Tansey (see J. T. ELlzey)<br />

J. Taylor (see M. Berbee)<br />

(see T. E. Chase)<br />

(see A. Gargas)<br />

J. W. Taylor (see M. Blackwell)<br />

(see S. B. Lee)<br />

(see S. B. Lee, paper #2)<br />

D. 0. TeBeest (see R. J. Chacko)<br />

B. Terhune (see T. W. Hill)<br />

D. TeStrake (see B. J. Cochrane)<br />

J. P. Tewari (see S. M. Boyetchko)<br />

L. L. Tews (see J. T. Ellzey)<br />

W. E. Tiberlake (see T. C. Sewall)<br />

M. B. Tobin (see P. L. Skatrud)<br />

R. C. Ullrich (see T. E. Chase)<br />

(see M. M. Stankis)<br />

E. M. Vadell (see M. T. Holmes)<br />

R. Vilgalys (see D. S. Hibbea)<br />

- (see E. Kay)<br />

(see S. Rehner)<br />

(see 0. K. Miller)<br />

T. J. Volk (see T. J. Leonard)<br />

C. J. K. Wang (see K. F. Lobuglio)<br />

G. J. Weidemann (see R. J. Chacko)<br />

T. P. Weiland (see R. K. Antibus)<br />

K. Web (see K. A. Jacobs)<br />

(see S. Digby)<br />

D. X. West (see A. E. Ubena)<br />

T. White (see M. Berbee)<br />

(see J. W. Taylor)<br />

P. W~dden (see M. Cooke)<br />

H. T. Wilkiason (see R. E. Wagner)<br />

J. D. Wood (see P. L. Skaaud)<br />

P. Wood (see C. Bradley)<br />

S. J. Wormsley (see T. J. Baroni)<br />

B. G. Yangco (see B. J. Cochrane)<br />

J. C. Zak (see D. A. Anders)<br />

P. ZQolawy (see R Pinette)<br />

Q. Zhai (see M. Chu-Chw)


Changes <strong>of</strong> Address and/or Phone Number<br />

ERIC W. A. BOEHM --- (612) 625 1756<br />

WILLIAM H. (BILL) BRANDT --- (503) 737-3451<br />

MARGARET M. CARREIRO --- Institute <strong>of</strong> Ecosystem Studies, BOX AB,<br />

Millbrook, NY 12545 -- (914) 677-5346<br />

LISA JOY CERLIGIONE -- (201) 751-4727<br />

CHESTER R. COOPER, JR --- Wadsworth Center for Laboratories and<br />

Research, NYS Department <strong>of</strong> Health, The Governor Nelson A.<br />

Rockefeller Empire State Plaza, P.O. Box 509, Albany NY 12201<br />

--(518) 486 3821<br />

DENNIS E. DESJARDIN --- Department <strong>of</strong> Biology, Oberlin College,<br />

Oberlin, OH 44074 -- (216) 775-8959<br />

STEPHANIE DIGBY --- Department <strong>of</strong> Plant Pathology, University <strong>of</strong><br />

Arkansas, Fayetteville, AR 72701 -- (501) 575-6772<br />

WILLIAM C. ELSIK --- Exxon Company, USA, P.O. Box 2189,<br />

Houston, TX 77252-2189 -- (713) 965-4516<br />

KARL ESSER --- phone 49-234-7002211 ; FAX 49-234-7002001<br />

MARIE L. FARR --- 13530 Sherwood Forest Drive, Silver Spring,<br />

Maryland 20904<br />

SHIGEHIRO KATO --- 18-1 Shinsakae-machi, Omihachiman-shi,<br />

Shiga-ken 523 Japan -- phone (0748) 33-7476<br />

BYONG KAK KIM --- (Seoul, Korea) -- New Phone No. = (02) 880-7864<br />

GARY F. LEATHAM --- Departments <strong>of</strong> Botany and Food Science, Birge<br />

Hall, University <strong>of</strong> Wisconsin, Madison, WI 53706 --<br />

(608) 262 1057<br />

JON POLISHOOK --- Merck, Sharp & Dohme Research Laboratories,<br />

P.O. Box 2000, R80Y-120, Rahway, New Jersey 07065-0900 --<br />

(phone?)<br />

JEFFREY POMMERVILLE --- Biology Department, Glendale College,<br />

6000 W. Olive Ave., Glendale, AZ 85302 -- (602) 435-3614<br />

ZAMIR K. PUNJA --- Department <strong>of</strong> Biological Sciences, Simon<br />

Fraser University, Burnaby, B.C., Canada V5A 1S6 --<br />

(604) 291-4471<br />

ROBERT W. ROBERSON --- Department <strong>of</strong> Botany, Arizona State<br />

University, Tempe, AZ 85257-1601 -- (602:? 965-8618<br />

CLARK T. ROGERSON -- (212) 220-8610


EMORY G. SIMMONS --- 717 Thornwood Road, Crawfordsville, IN<br />

47933 -- (317) 364-1992<br />

WALTER J. SUNDBERG --- Department <strong>of</strong> Plant Biology (new<br />

department name only), Southern Illinois University,<br />

Carbondale, Illinois 62901 -- (618) 453-3212 (on weekends and<br />

after hours; otherwise, old number still usable M-F, 8-5)<br />

K. SURYANARAYANA -- Department <strong>of</strong> Microbiology, University <strong>of</strong><br />

Virginia School <strong>of</strong> Medicine, Box 441, Jordan Hall,<br />

Charlottesville, Virginia 22908 -- (804) 924-9991<br />

RODHAM E. TULLOSS (spelling correction ,<strong>of</strong> Rodham) --<br />

(609) 448-5096 (home) ; (609) 639-6116 (<strong>of</strong>fice)<br />

Forthcoming Events<br />

INTERNATIONAL MYCOLOGICAL CONGRESS IV, Regensburg, August 23-<br />

September 3, 1990.<br />

Fifth International Symposium on the Microbiology <strong>of</strong> the<br />

Phyllosphere:<br />

31 July - 3 August 1990. Fifth International Ssmwsium on<br />

the Microbiology <strong>of</strong> the Phyllosphere. To be held at Madison,<br />

Wisconsin. Attendance limited to about 100 persons. Topics<br />

include fungal epiphytes and endophytes, and fungi <strong>of</strong> medical<br />

importance found on leaf surfaces. For information contact:<br />

John Andrews, Plant Pathology Department, University <strong>of</strong><br />

Wisconsin, 1630 Linden Dr., Madison, WI 53706. Tel (608)<br />

262-9642; fax (608) 263-2626; E-mail AndrewsJeWISCMACC.<br />

Sixth International Marine Mycology Symposium -- August, 1993 --<br />

Tampa/St . Petersburg, Florida. Contact : David Porter or<br />

Diane Te Strake.<br />

PENNSYLVANIA STATE UNIVERSITY:<br />

A Specialty Mushroom Workshop will be held on Wednesday, June 13,1990 at The<br />

Pennsylvania State University. The purpose <strong>of</strong> the workshop is to promote the exchange<br />

<strong>of</strong> ideas for research, production and merchandizing <strong>of</strong> specialty mushrooms (Shiitake,<br />

.Pleurotus, etc). The Specialty Mushroom Workshop will directly follow the 32nd<br />

Mushroom Industry Short Course scheduled for June 1 lth and 12th, 1990. For more<br />

information on both the Specialty Mushroom Workshop and the 32nd Mushroom Industry<br />

Short Course contact:<br />

Agricultural Conferences and Short Courses<br />

306 Agricultural Administration Building<br />

Pennsylvania State University<br />

University Park, PA 16802<br />

(8 14) 865-8301


MAGGIE ROGERS notifies us that the North <strong>America</strong>n <strong>Mycological</strong><br />

Association's annual foray will be in Whistler, BC, Canada,<br />

October 4-7, 1990.<br />

There will be a working conference on Agaricus biology<br />

relating to spawn biotechnology; early October, 1990, at the<br />

University <strong>of</strong> Toronto, Erindale Campus. Contact: RICHARD<br />

KERRIGAN or PAUL HORGEN for more information.<br />

GRANTS for Shade Tree Research. Each year since 1975, the<br />

International <strong>Society</strong> <strong>of</strong> Arboriculture has awarded grants for<br />

research on shade trees. Usually fifteen $1500 grants per year<br />

are awarded. Proposals must be received by December 1st each<br />

year. For further information, reply to Shade Tree Labora-<br />

tories, University <strong>of</strong> Massachusetts, Amherst, MA 01003.<br />

<strong>Mycological</strong> Services Available<br />

PARTHA BANERJEE will identify specimens <strong>of</strong> Pluteus, Section<br />

Pluteus; notes and/or photos helpful but not required.<br />

(Department <strong>of</strong> Plant Biology, Southern Illinois University,<br />

Carbondale, Illinois 62901)<br />

MICHAEL CASTELLANO has <strong>of</strong>fered to identify hypogeous basidio-<br />

mycetes.<br />

TERESITA ITURRIAGA <strong>of</strong>fers to identify tropical discomycetes.<br />

HAROLD W. KELLER will identify myxomycetes from living trees, and<br />

any specimens from Arkansas.<br />

RICHARD KERRIGAN <strong>of</strong>fers to verify identities <strong>of</strong> Rgaricur<br />

bzsporus and allied species (Section #ortenses) .<br />

DANA L. RICHTER has cultures and specimens <strong>of</strong> Scleroderma spp.<br />

(Gasteromycetes) .<br />

MICHAEL G. RINALDI <strong>of</strong>fers, for Federal agencies, to identify and<br />

to do medical mycological testing <strong>of</strong> fungi. Contact him at the<br />

Veterans Affairs Mycology Reference Laboratory, VA Hospital,<br />

San Antonio, TX 78284.<br />

WALTER J. SUNDBERG will identify specimens <strong>of</strong> L@piota sensu<br />

lato; notes and/or photos helpful but not required.<br />

RODHAM E. TULLOSS <strong>of</strong>fers to identify collections <strong>of</strong> Amanita.<br />

Please query first; field notes and/or color slide would be<br />

very desirable.


Fungi Wanted<br />

K. R. ANEJA wants pathogenic fungi <strong>of</strong> water hyacinth and<br />

Parthenium hyster-ophorus.<br />

J. L. BAPTISTA-FERREIRA wants cultures or specimens for isolation<br />

<strong>of</strong> Lenrite.~ betuiina, L . warnieri, Pycnosporus cinnetharinus,<br />

and Trametes gubarskii .<br />

DAVID BERMUDES wants specimens <strong>of</strong> bioluminescent fungi<br />

(especially Hycena spp.) .<br />

MICHAEL CASTELLANO wants hypogeous fungi from tropical countries.<br />

ALICE W. CHEN would like to receive (1) homokaryotic cultures <strong>of</strong><br />

Ganoderme spp., including G, iucidum (or cultures <strong>of</strong><br />

6. curtisii , the "old" name) and G. tsugae , and (2)<br />

dikaryotic cultures from which the homokaryotic cultures were<br />

derived.<br />

DENNIS E. DESJARDIN wants specimens and cultures <strong>of</strong> Warasmius,<br />

Marasmiell us and tdicromphaie (Basidiomycetes, Agaricales,<br />

Tricholomataceae) from the Gulf Coast region.<br />

JOHN LOUIS HARRIS wants cultures <strong>of</strong> psychrophilic , carotenoid-<br />

producing fungi sent to him.<br />

TERESITA ITURRIAGA wants specimens <strong>of</strong> the genus Pseudospiropes<br />

(Hyphomycet es) .<br />

HAROLD W. KELLER wants any myxomycetes from Arkansas.<br />

RICHARD KERRIGAN wants cultures/spore prints <strong>of</strong> wild Rgaricus<br />

bisporus and allied species (Section Hortenses) . Vouchers<br />

are preferred, but not essential.<br />

REINHOLD MANKAU wants isolates <strong>of</strong> nematode-trapping hyphomycetes<br />

(Arthrohotrys, Monacrosporium, Dactylaria), and endoparasitic<br />

fungi attacking nematodes. His laboratory is trying to build a<br />

national collection.<br />

H. P. MOLITORIS wants marine basidiomycetes and other marine<br />

fungi from a depth below 200 meters.<br />

DON PRUSSO wants specimens <strong>of</strong> Tulostoma and/or collection<br />

data and locations <strong>of</strong> collections available for study. He will<br />

be travelling through Montana, South and North Dakota,<br />

Minnesota, Wisconsin, Michigan, Wyoming, and northern Nebraska<br />

during June and July collecting Tuiostoma and visiting any<br />

herbaria that have collections <strong>of</strong> this genus. He asks that you<br />

PLEASE let him know if you have specimens.<br />

DANA L. RICHTER wants (or will trade) specimens <strong>of</strong> ScJeroderma<br />

(Gast eromycetes) and records <strong>of</strong> occurrence.


STEVEN L. STEPHENSON wants collections <strong>of</strong> myxomycetes, especially<br />

from areas <strong>of</strong> the world other than North <strong>America</strong>.<br />

DIANE TE STRAKE wants isolates <strong>of</strong> Basidioholus sent to her.<br />

RODHAM E. TULLOSS wants specimens <strong>of</strong> Amanita Section Amidella<br />

<strong>of</strong> Canada and Mexico (e.g.,Amanita volvata s.l., and<br />

Amanita peckiana s.l., or possibly diagnosed previously as<br />

A. ponderosa, A. lepiotoides, A. valeus, etc.).<br />

JORGE E. WRIGHT wants specimens <strong>of</strong> South <strong>America</strong>n gasteromycetes,<br />

especially members <strong>of</strong> the Lycoperdales and Tulostomatales would<br />

be greatly appreciated.<br />

Publications and Computer Programs<br />

for Give-Away , Sale, or Exchange<br />

E. S. BENEKE reported that Floyd M. Clum (810 N. West St., Falls<br />

Church, Virginia 22046 -- phone 703-532-3147) has unbound<br />

volumes <strong>of</strong> Mvcolouiq as follows: 1948, 1949 (July-August<br />

missing), 1950-1974 and 1975 (January-February missing). He<br />

also has most copies <strong>of</strong> Phvto~atholoqy from 1948-1963.<br />

WILLIAM R. BURK has a variety <strong>of</strong> publications and/or computer<br />

programs for sale. Please write to him for a listing.<br />

GREGOIRE LAURENT HENNEBERT has available MUCL List <strong>of</strong> Cultures<br />

<strong>of</strong> Fungi (Yeasts Included). +/- 5000 strains. 600 FB = +/-<br />

$15.00 U.S.<br />

JEROME MOTTA has authored -- A Proqrammed Guide for the<br />

Cultivation <strong>of</strong> Funqi . It ii available from Mycotechnology<br />

Services, 43 Randolph Road, Suite 145, Silver Spring, Maryland<br />

20904. Guide Program plus User's Manual, $59.95; Demonstration<br />

Disk, $5.00; User's Manual only, $10.00.<br />

FRED RHOADES is building a library <strong>of</strong> the location <strong>of</strong> synoptic<br />

keys developed with PC-TAXON. COMPress (the distributor <strong>of</strong><br />

PC-TAXON) will include the library listing with the program<br />

when sold, and publish it from time to time in their newslet-<br />

ter. Please let him know <strong>of</strong> any keys you have to share with<br />

other readers. For each key, indicate (1) author, (2) taxon-<br />

omic group, (3) key title, (4) nwnber <strong>of</strong> taxa, (5) .KEY size,<br />

(6) .DES size, and (7) a description <strong>of</strong> for whom the key was<br />

written, or for what applications it would be useful. All<br />

contributors will receive the library listing and be put on a<br />

mailing list for periodic update^.


HAGGIE ROGERS has back issues and current subscriptions to --<br />

Mushroom, Thg Journal <strong>of</strong> Wild Mushrooming. Back issues are<br />

$4.00 each, or $3.00 each for 3 or more copies. Though written<br />

for amateurs, issues regularly contain pr<strong>of</strong>essionally written<br />

articles on mushrooms and fungi-related topics. Editor's<br />

Note: Maygie sent two samples with her questionnaire, and they<br />

are very interesting reading,<br />

DIANE TE STRAKE has for sale (best <strong>of</strong>fer) : (1) The Genera <strong>of</strong><br />

Funqi, 1957, Clements and Shear; (2) The Pyrenomycetous Funqi,<br />

1975, Wehmeyer; (3) A_ Manual <strong>of</strong> Soil Funqi, 1945, Gilman;<br />

(4) The Funqi, Volumes I and I1 (Second Printings, 1948 and<br />

1949) , Wolf and Wolf.<br />

ABRAHAM WEINTRAUB has for sale -- Bacterial Chemistry<br />

Physioloqy (1950) by John Roger Porter. $25.00 + shipping.<br />

(Address below in Employment Desired.)<br />

New Books .by Members<br />

CASTELLANO, M . A. , and J . M. TRAPPE. (Date?) . ky LQ 2bsxes ~f<br />

Qe Genera <strong>of</strong> Hvpoueous hnSi 9f M&h Zemerats Esuxz&s. Mad<br />

River Press, Eureka, CA. 186 pages, $24.95.<br />

MOORE-LANDECKER, ELIZABETH. 1990. Fundamentals <strong>of</strong> the Funsi,<br />

3rd edition. Prentice Hall, Englewood Cliffs, NJ 07632.<br />

MEHROTRA, R. S., and K. R. ANEJA. 1990. &J Introduction to<br />

Mvcoloqy. Wiley Eastern, Ltd., New Delhi, India.<br />

Publications Needed<br />

WILLIAM R. BURK needs a copy <strong>of</strong> the 1969 publication, Oft Told<br />

Mushroom Recipes (from the Puget Sound <strong>Mycological</strong> <strong>Society</strong>) ,<br />

and any children's books on fungi and mushrooms.<br />

MARGARET M. CARREIRO needs (1) A Manual <strong>of</strong> the Penicillia by K.<br />

Raper and C. Thom, (2) Die Mucorales, by H. Zycha, R. Siepmann,<br />

and G. Linneman, and (3) A_ Compendium <strong>of</strong> Soil Funqi by Domsch,<br />

W. Gams, and T. Anderson,<br />

WILLIAM C. ELSIK needs any reprints dealing with spore or septa1<br />

morphology.<br />

JOHN LOUIS HARRIS needs any publications dealing with carotenoid-<br />

producing fungi.


RICHARD KERRIGAN needs anything on taxonomy or distributions <strong>of</strong><br />

Agaricus spp., and old mushroom spawn catalogs.<br />

DANA. L. RICHTER needs reprints with records <strong>of</strong> Scleroderra spp.<br />

(Gasteromycetes) and associated hosts.<br />

JOHANNES A. SCHMITT needs (1) publications about heavy metals and<br />

radioactivity in wild mushrooms, and (2) Mvcolocria volumes<br />

before 1985.<br />

EMORY G. SIMMONS needs -- Mvcoloqia, vols. 43 and 44 (1951-52).<br />

STEVEN L. STEPHENSON needs reprints on myxomycetes.<br />

RODHAM E. TULLOSS needs (1) Mushroom Poisoninq by Link<strong>of</strong>f and<br />

Mitchell, and (2) reprints concerning Amanita from non-U.S.<br />

journals <strong>of</strong> Western Hemisphere.<br />

Vacancies for Mycologists<br />

THE UNIVERSITY OF TEXAS AT AUSTIN: A Postdoctoral Position is<br />

available immediately to study at the molecular level the iron-<br />

stress response <strong>of</strong> plants and plant-iron nutrition, as mediated<br />

by microbial siderophores and phytosiderophores. Preference<br />

will be given to applicants having prior experience with<br />

recombinant DNA methods relevant to plant genes, including<br />

techniques involving immunodetection <strong>of</strong> fusion proteins,<br />

Western and Northern blotting or plant transformation. A<br />

candidate might alternatively be considered who has experience<br />

with cloning <strong>of</strong> genes from fungi. Please send curriculum<br />

vitae, cover letter, and telephone numbers <strong>of</strong> three references<br />

to DR. PAUL J. SZANISZLO, Department <strong>of</strong> Microbiology,<br />

University <strong>of</strong> Texas at Austin, Austin, TX 78712.<br />

Assistantships and Fellowships<br />

HARVARD UNIVERSITY: Fellowships including full tuition and<br />

stipends are available to graduate students applying to the<br />

Department <strong>of</strong> Organistic and Evolutionary Biology. Contact<br />

DONALD H. PFISTER.<br />

SUNY COLLEGE OF ENVIRONMENTAL SCIENCE AND FORESTRY: Research and<br />

Teaching Assistantships available to graduate students inter-<br />

ested in systematics, physiology, ultrastructure, ecology,<br />

molecular biology, and genetic engineering <strong>of</strong> fungi, or forest<br />

pathology , wood products pathology, or mycorrhizae. Contact<br />

C.J.K. WANG, D.H. GRIFFIN, J.J. WORRALL, S.O. ROGERS, or W.A.<br />

POWELL, SUNY College <strong>of</strong> ESF, Syracuse, NY 13120.


Employment Desired<br />

K. R. ANEJA would like a research and/or teaching position.<br />

ERIC W. A. BOEHM desires a post-doctoral position studying<br />

karyotypes in the Uredinales using molecular biology tech-<br />

niques. He is expecting to finish his Ph.D. degree in 1991<br />

with DR. B. BUSHNELL (Minnesota, St. Paul) .<br />

JOHN DADA would like to have an opportunity to do some postdoctoral<br />

research with agarics, polypores, and gasteromycetes.<br />

Dr. Dada completed his Ph.D. in Nigeria (19891, and would like<br />

to spend 6-9 months studying in the U.S. prior to returning to<br />

Nigeria and working on Nigerian fungi. Copies <strong>of</strong> Dr. Dada's<br />

letter and curriculum vitae can be obtained from the M a<br />

- Newsletter Editor.<br />

ABRAHAM WEINTRAUB is very interested in part-time (no travel)<br />

employment which will allow him to work at home preparing water<br />

extracts for various experimental culture media used in studies<br />

<strong>of</strong> nutritional requirements, 'growth promotion, sporulation,<br />

seed germination, etc. He has his own equipment and new<br />

techniques for both mycology and botany. Extracts are filtered<br />

and sterile. He will prepare sterile solutions or sterile sand<br />

for inoculation and suspension <strong>of</strong> fungal spores. A new wetting<br />

agent is also available in sterile solution if desired.<br />

Address: 2034 E 21st St., Brooklyn, New York 11229<br />

DANIEL A. WUBAH is looking for an assistant pr<strong>of</strong>essorship or a<br />

post-doctoral position. He expects to complete his Ph.D, in<br />

June, 1990. His research has dealt with development <strong>of</strong><br />

anaerobic, zoosporic fungi from the rumens <strong>of</strong> cattle, and has<br />

been supervised by M. S. Fuller, University <strong>of</strong> Georgia.<br />

Major Honors, Awards, and Promotions<br />

K. R. ANEJA was promoted to the position <strong>of</strong> Reader in the<br />

Department <strong>of</strong> Botany, Kurukshetra University, India.<br />

JOAN W. BENNETT was elected President <strong>of</strong> the <strong>America</strong>n <strong>Society</strong> for<br />

Microbiology, 1990-91.<br />

KARL ESSER was awarded the Chevalier des Palmes Acadgmiques,<br />

Republique Francaise (Knight <strong>of</strong> the French Order for<br />

Scientists: Academic Palms).<br />

BYONG KAK KIM received in 1988 the Seug Ji Award for Outstanding<br />

Research in Mycology from the Korean <strong>Society</strong> <strong>of</strong> Mycology.<br />

MICHAEL G. RINALDI was promoted to Pr<strong>of</strong>essor <strong>of</strong> Pathology and<br />

Medicine, effective September 1, 1989, at the University <strong>of</strong><br />

Texas Health Science Center, San Antonio.


WALTER J. SUNDBERG recently was named "Outstanding Teacher,<br />

College <strong>of</strong> Science" at Southern Illinois University. This<br />

teaching honor is bestowed on only one <strong>of</strong> the 100+ faculty in<br />

the College <strong>of</strong> Science each year.<br />

MARVIN D. WHITEHEAD (Emeritus Member <strong>of</strong> MSA) reported that he had<br />

been awarded in 1948 a departmental scholarship by the University<br />

<strong>of</strong> Wisconsin, Madison.<br />

Changes Affiliation Status<br />

ERIC W. A. BOEHM presently is in the Cereal Rust Laboratory,<br />

USDA, ARS (University <strong>of</strong> Minnesota)<br />

BILL BRANDT will retire on June 30, 1990; he will retain the use<br />

<strong>of</strong> his <strong>of</strong>fice and laboratory for three subsequent years, and<br />

intends to continue research on Ucrticillium.<br />

MARGARET M. CARREIRO has taken a position as a Postdoctoral<br />

Associate at the Institute <strong>of</strong> Ecosystem Studies, Millbrook, NY.<br />

LISA JOY CERLIGIONE is now at Merck, Sharp & Dohme Research<br />

Laboratories, Rahway, New Jersey.<br />

MARTHA CHRISTENSEN has retired from teaching at the University <strong>of</strong><br />

Wyoming, but will remain in the Department <strong>of</strong> Botany, and at<br />

work on ecological aspects <strong>of</strong> soil fungi and Psnicillium<br />

systematics and ecology, with support from industry and the<br />

University.<br />

CHESTER R. COOPER, JR. recently completed his Ph.D. under the<br />

supervision <strong>of</strong> Paul Szaniszlo, and has taken a position as<br />

Research Scientist at the Wadsworth Center for Laboratories and<br />

Research, NYS Department <strong>of</strong> Health, Albany, NY. His thesis was<br />

Induced parasexual senetic analysis <strong>of</strong> the imperfect pathosen<br />

- <strong>of</strong> humans, WangieXla dcrmatitidis.<br />

DENNIS E. DESJARDIN has accepted a position as Visiting Assistant<br />

Pr<strong>of</strong>essor <strong>of</strong> Biology at Oberlin College, Oberlin, OH.<br />

ROBERT FOGEL in November, 1989, moved into a new laboratory<br />

for fungal molecular systematics housed in the University<br />

<strong>of</strong> Michigan Herbarium.<br />

AL FUNK retired from the Pacific Forestry Center, Victoria, B.C.<br />

in February, 1990.<br />

GARY F. LEATHAM has moved to a new faculty position in the<br />

Departments <strong>of</strong> Botany and Food Science, University <strong>of</strong><br />

Wisconsin, Madison, WI.


JON POLISHOOK is now at Merck, Sharp, & Dohme Research<br />

Laboratories, Rahway, New Jersey.<br />

JEFFREY POMMERVILLE is a member <strong>of</strong> the Biology Department at<br />

Glendale College In Glendale (Phoenix) , AZ.<br />

ZAMIR K. PUNJA has joined the Department <strong>of</strong> Biological Sciences<br />

at Simon Fraser University, Burnaby, B.C., as Associate<br />

Pr<strong>of</strong>essor <strong>of</strong> Plant Pathology/Biotechnology, July 1, 1989.<br />

ROBERT W. ROBERSON has taken a position as Assistant Pr<strong>of</strong>essor <strong>of</strong><br />

Botany at Arizona State University, Tempe, AZ 85287-1601.<br />

HARRY THIERS retired from San Francisco State University in<br />

January, 1989. Upon his retirement, the University named the<br />

herbarium in his honor.<br />

Notes and Comments<br />

ERIC W. A. BOEHM wishes to know whether anyone in MSA has had<br />

experience using computer image analysis from serial TEM<br />

sections in reconstructing pachytene karyotypes Care such<br />

systems available for use?). Also, he needs to know whether<br />

anyone has experience using confocal (scanning laser light)<br />

microscopy, and can recommend any DNA-binding fluorochromes<br />

for examination <strong>of</strong> fungal nuclei in meiotic pachytene.<br />

FRANCOISE CANDOUSSAU appeals to the generosity <strong>of</strong> the MSA<br />

membership in order to found the first Mycoloqical <strong>Society</strong> <strong>of</strong><br />

Rumania. He begs MSA members to send all they can spare <strong>of</strong>-<br />

their books and mycological publications to Dr. Mihai Toma, to<br />

create the first mycological library in Rumania (Iasi). It<br />

could not be founded before because <strong>of</strong> the dictatorship.<br />

Dr. Mihai TOMA, Institutul Agronomic, Catedra de Botanica,<br />

R.6600-IASI-6, Rumania.<br />

MARTHA CHRISTENSEN reported that the "Second International<br />

Penici l .l ium and Aspergill us Workshop" was held in Baarn<br />

in early May, 1989. It was organized by Rob Samson and others<br />

at CBS. Those attending from the U.S. and Canada included,<br />

M. A. Christensen, M. Klich, E. Mullaney, S. Peterson, K. A.<br />

Seifert, and J. W. Taylor.<br />

Cultures in the late Kenneth B. Raper's collections <strong>of</strong> isolates<br />

in Rspergillus, the 440-membered "WB" Collection referred<br />

to in Genus Aspergillus (Raper and Fennell, 1965), can<br />

now be obtained from ATCC, CBS, CMI and the University <strong>of</strong><br />

Alberta Micr<strong>of</strong>ungus Collection. Anyone interested in a<br />

listing, by species and WB number, showing specific deposition<br />

<strong>of</strong> the lyophilized preps made in 1964 may write to Dr. Martha<br />

Christensen, Department <strong>of</strong> Botany, P.O. Box 3165, University<br />

Station, University <strong>of</strong> Wyoming, Laramie, Wyoming 82071, USA.


TERRENCE M. HAMMILL is Acting Chairman, Department <strong>of</strong> Biology at<br />

SUNY-Oswego.<br />

HAROLD W. KELLER sent a short article he wrote for the Arkansas .<br />

<strong>Mycological</strong> <strong>Society</strong> Newsletter. I have reproduced a part <strong>of</strong> it<br />

below as a request for directions to apple orchards and special<br />

habitats for myxomycetes in the eastern United States.<br />

SPECIAL COLLECTING SITES IN ARKANSAS<br />

Our research on the Myxomycetes <strong>of</strong> Arkansas began over 30 years ago and<br />

continues to yield species new to science or <strong>of</strong> special interest.<br />

Pr<strong>of</strong>essors James H. Hutchison .from Arkansas State University at Jonesboro<br />

and Uno Eliasson from the University <strong>of</strong> Gothenburg, Gothenburg, Sweden are<br />

actively involved with this research project. Directions to productive<br />

collecting areas would help us expand our coverage and exploration<br />

throughout Arkansas. For example, plantings <strong>of</strong> Red Cedar trees in<br />

cemeteries or apple trees in apple orchards provide ideal sites for mxyos.<br />

These trees should be 30 or more years old to be really productive. Myxo<br />

sporangia develop on the main trunk axis and lateral branches, extending up<br />

into the crown <strong>of</strong> the tree. Given optimal conditions <strong>of</strong> temperature and<br />

rainfall, myoxs occur on living trees and vines in great pr<strong>of</strong>usion,<br />

sometimes providing scattered sporangia covering an area <strong>of</strong> several feet.<br />

Collection instructions are available upon request.<br />

DONALD H. PFISTER volunteers to act as a clearing house for any<br />

member <strong>of</strong> MSA who wants to give their Mycoloqia to an institu-<br />

tion in a developing country.<br />

RICHARD P. KORF reported that Andrea Irene Romero <strong>of</strong> the<br />

University <strong>of</strong> Buenos Aires, Argentina, has accepted an Anna E.<br />

Jenkins Predoctoral Fellowship in the Cornell University Plant<br />

Pathology Herbarium in the summer <strong>of</strong> 1990.<br />

GLORIA and FRED RHOADES announce the birth <strong>of</strong> a daughter, Emily,<br />

on October 19, 1989.<br />

WALTER J. SUNDBERG organized and hosted the annual Alexander'H.<br />

Smith (midwest mycologist's) Foray and the annual meeting and<br />

foray <strong>of</strong> the North <strong>America</strong>n <strong>Mycological</strong> Association this past<br />

fall at Touch <strong>of</strong> Nature, Southern Illinois University's outdoor<br />

laboratory facility near Carbondale, Illinois.<br />

MICHAEL TANSEY and the MSA Teaching Committee request informa-<br />

tion about new mycology textbooks not included in the Committee's<br />

1989 survey about mycology textbooks.<br />

ABRAHAM WEINTRAUB has for sale a Revival Electric Table-Top<br />

Sterilizer Model No. 12 in perfect working condition. (Address<br />

above in Employment Desired.)


JORGE E. WRIGHT reported that Drs. David Minter and Paul Cannon<br />

(IMC) visited the Laboratorio de Micologia, Dept. de Ciencias<br />

Biologicas, University <strong>of</strong> Buenos Aires, Argentina, during their<br />

month-long visit to Argentina. Minter and Cannon organized the<br />

I1 International Course on Ascomycetes, attended by 15 graduate<br />

students from Argentina, Uruguay and Brazil, and sponsored by<br />

the CONICET-Royal <strong>Society</strong> agreement.<br />

--Dr. Mario Rajchenberg spent two months in New Zealand'working<br />

with Dr. P. Buchanan on polypores as part <strong>of</strong> his Guggenheim<br />

Fellowship . Later he worked at BPI and NYBG, and visited<br />

other laboratories in the USA.<br />

--Voronica Suarez (a graduate student directed by J. Wright) has<br />

worked on "Lycoperdales <strong>of</strong> Southern South <strong>America</strong>." A mono-<br />

graph <strong>of</strong> Ahseoma has been sent to press.<br />

--Laura D. de Yoledo recently has obtained her Ph.D. degree at<br />

the University <strong>of</strong> Cordoba (Argentina) with her thesis on the<br />

"Gasteromycetas <strong>of</strong> Center and Northwest Argentina."<br />

--Clarice Loguercio Leite, University <strong>of</strong> Florianopolis, Brazil,<br />

is finishing her thesis on the polypores <strong>of</strong> the Island <strong>of</strong> Santa<br />

Catarina. She is a Fellow <strong>of</strong> the Brazilian Government, working<br />

for her Ph,D. at the University <strong>of</strong> Buenos Aires.<br />

--Dr. Monica Adler is working as a Research Associate <strong>of</strong> the<br />

Argentine National Research Council on the Parmeliaceae <strong>of</strong> the<br />

Province <strong>of</strong> Buenos Aires.<br />

--Nora Scutari is working as a Research Associate <strong>of</strong> the Buenos<br />

Aires Provincial Research Council on her thesis about<br />

Physciaceae and Telochistaceae <strong>of</strong> Buenos Aires.<br />

L<br />

WANTED (ALIVE, PLEASE):<br />

A GA RlCUS BISPORUS<br />

A reward <strong>of</strong> up to $1 00 (US), plus costs, is <strong>of</strong>fered<br />

for cultures or viable spores <strong>of</strong> collections <strong>of</strong><br />

A. bisporus (= A. brunnescens?) and certain<br />

related species. For details contact:<br />

R. W. Kerrigan, Erindale Botany, University <strong>of</strong><br />

Toronto, Mississauga, ONT, CANADA L5L 1 C6<br />

i 1


DON PFISTER sent along the following information about the BIOSIS<br />

CONNECTION, suggesting that it be published in the Newsletter.<br />

THE BIOSIS CCYNECTION<br />

Biological Unity Throuqh Communications<br />

The glory <strong>of</strong> the life sciences lies in their diversity. The<br />

coverage list <strong>of</strong> BIOLOGICAL ABSTRACTS shows over 9,000 journals<br />

published by (or for) thousands <strong>of</strong> scientific societies. Its<br />

companion publication, BIOLOGICAL ABSTRACTSIRRM (REPORTS,<br />

REVIEWS, MEETINGS) reports on more than 1,000 meetings (s~onsored<br />

by a society) each year.<br />

Still, this array <strong>of</strong> organizations has suffered from its diver-<br />

sity in that the life sicences have not coalesced to form the<br />

large powerful member organizations found in our sister sciences<br />

<strong>of</strong> chemistry, physics, medicine, and others.<br />

This historical pressures that account for this phenomenon were<br />

at least temporarily absent in 1927 when several societies con-<br />

cluded a 10 year period <strong>of</strong> preparation (1) and incorporated<br />

BIOLOGICAL ABSTRACTS, INC. (BIOSIS) as the not-for-pr<strong>of</strong>it cor-<br />

oration it remains today. Since that time BIOSIS has provided a<br />

degree <strong>of</strong> unification among diversity by becoming the preeminent<br />

abstracting and indexing service for the life sciences. (2)<br />

Now more than 60 years later, BIOSIS has developed a new service,<br />

the BIOSIS CONNECTION, whose scope rivals the ambitious goals <strong>of</strong><br />

the 1927 founders.<br />

BIOSIS is proud to include the <strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> <strong>America</strong><br />

among the early adherents to the BIOSIS CONNECTION conce~t<br />

through its membership in the BIOSIS CONNECTION Affiliate<br />

Program.<br />

Recognizing the benefits and problems <strong>of</strong> diversity, the BIOSIS<br />

CONNECTION will employ'modern information technology as a focal<br />

point for life science communications.<br />

The first component <strong>of</strong> the BIOSIS CONNECTION concept to be imple-<br />

mented is a computer-based, online information retrieva1,service.<br />

With rare exceptions, the provision <strong>of</strong> online information<br />

retrieval services has been dominated by commercial interests. .<br />

The BIOSIS CONNECTION is beinq implemented by a not-for-pr<strong>of</strong>it<br />

organization with many years <strong>of</strong> experience in this technology.<br />

It will provide a sensitivity toward the scientific needs <strong>of</strong> our<br />

colleagues.<br />

As a not-for-pr<strong>of</strong>it activity, the CONNECTION expects to operate<br />

in a more favorable economic posture. Pr<strong>of</strong>it oriented, add-on<br />

charges will not be necessary, and the corporate overheads<br />

present in many commercial services will not be applied.<br />

The CONNECTION provides several specially prepared databases<br />

derived from BIOSIS resources. The nature and scope <strong>of</strong> these<br />

databases were defined by extensive market analysis and include<br />

files <strong>of</strong> general research papers, patents. books and meetings.<br />

Other subject-specific and general information files have also<br />

been added.


Mechanisms are being built into the CONNECTION that will act to<br />

generate business and sales <strong>of</strong> society publications and services.<br />

In addition to the display <strong>of</strong> information on books, journals,<br />

meetings, course <strong>of</strong>ferings, etc., the system includes ~rocedures<br />

for online (direct or indirect) ordering <strong>of</strong> these items.<br />

Recognizing that "computer literacy" varies widely among life<br />

scientists, the BIOSIS CONNECTION allows two modes <strong>of</strong> access to<br />

its information. A "menu" system is self-instructing and<br />

requires no prior experience in online retrieval. An "expert"<br />

system is also present for those with the requisite background.<br />

/ The online system(3) are but a part <strong>of</strong> an eventual arra.y <strong>of</strong><br />

services to facilitate business, publication, and scientific<br />

needs as a service to our community.<br />

A key element in planning and development for the BIOSIS CON-<br />

NECTION, the new Affiliate Program (which MSA has joined)<br />

includes a variety <strong>of</strong> coportunities for life science organiza-<br />

tions. Affiliates are encouraged to provide input concerning new<br />

publications, meeting information, employment opportunities, and<br />

other useful facts to be carried as parts <strong>of</strong> the BIOSIS CONNEC-<br />

TION online database.<br />

The addition <strong>of</strong> databases will be integrated by Affiliate<br />

advisory procedures, and candidates are sought for the CONNECTION.<br />

Once evaluation has been completed, a variety <strong>of</strong> database su~port<br />

methods are available. Scientifically critical material may<br />

receive full or partial funding from BIOSIS CONNECTION resources.<br />

Cooperative projects will be encouraged, and <strong>of</strong> course, outside<br />

sponsorship can be utilized. While resources are limited, t.he<br />

CONNECTION plans for referral databases which will record<br />

collections <strong>of</strong> information available, together with their loca-<br />

tions and conditions. for use.<br />

As a further incentive to the Affiliate Program, BIOSIS will pro-<br />

vide CONNECTION services at discounted rates to members <strong>of</strong> Affili-<br />

ate Program societies.<br />

The BIOSIS Board Trustees has endorsed the BIOSIS CONNECTION<br />

concept by providing multi-year funding for the basic online<br />

service. This commitment to communications as a means <strong>of</strong><br />

achieving unification among diversity provides life scientists all<br />

over the world with a focal point that will benefit the advance-<br />

ment <strong>of</strong> research.<br />

For further inf5rmation ........................................<br />

(1 ) W.C. Steere: BIOLOGICAL ABSTRACTS/BIOSIS pp 1-3, Plenum Press<br />

1976.<br />

(2) The BIOSIS database contains more than eight million records<br />

BIOSIS will abstractlindex over 530,000 reports in 1989.<br />

A.M. Elias<br />

Director<br />

Marketing & Distribution Division


FUNGAL COLLECTION AT THE UNIVERSITY OF NEBRASKA STATE MUSEUM<br />

by Margaret R. Bolick. Curator and<br />

Charles L. Messenger, Collections Manger<br />

The Division <strong>of</strong> Botany <strong>of</strong> the University <strong>of</strong> Nebraska State<br />

Museum (UNSM) consists <strong>of</strong> the 300,000 specimen C.E. Bessey<br />

Herbarium (Herbarium acronym: NEB) and a small paleobotanical<br />

collection. The fungal collections-were ranked as 25th in size<br />

nationally by Payen et al. (19741. At that time there were an<br />

estimated 30,000 specimens. Our current best estimate <strong>of</strong> the size<br />

<strong>of</strong> the fungal collections after the addition <strong>of</strong> specimens from the<br />

Department <strong>of</strong> Plant Pathology is between 50,000 and 60,000<br />

specimens.<br />

HI STORY<br />

The antecedent <strong>of</strong> the present University <strong>of</strong> Nebraska State<br />

Museum was mandated by the Board <strong>of</strong> Regents at their first meeting<br />

in 1871. Samuel Aughey was appointed the first pr<strong>of</strong>essor <strong>of</strong><br />

natural history in 1874 By 1875 he had produced a "Catalog <strong>of</strong><br />

the Flora <strong>of</strong> Nebraska." William Cleburne, however, soon became<br />

the major contributor <strong>of</strong> specimens to the herbarium. Beginning in<br />

the 18701s, Cleburne collected actively for the herbarium until<br />

the turn <strong>of</strong> the century.<br />

The herbarium began to .flourish when Charles E. Bessey was<br />

hired in 1886. Although Bessey contributed relatively few<br />

specimens to the herbarium himself, his students became indefati-<br />

gable collectors and a strong exchange program was maintained.<br />

Several <strong>of</strong> Besseyls students went on to become prominent<br />

mycologists; among these were his son Ernst A. Bessey, Frederick<br />

E. Clements, Cornelius L.Shear, and Frederick A. Wolf.<br />

The group <strong>of</strong> Besseyls students established the "Botanical<br />

Seminar" or "Bot. Sem." that took as its project a botanical<br />

survey <strong>of</strong> the state. Rosc,oe Pound and Frederick Clements col-<br />

laborated on collections <strong>of</strong> fungi during this ~eriod. Clements<br />

named many new species in the four issues <strong>of</strong> the Report <strong>of</strong> the<br />

Botanical Survey qf Nebraska (1892-1896). Many o f e z s r<br />

fungal holotypes collected during this early period are deposited<br />

at NEB.<br />

FUNGAL COLLECTIONS AT NEB<br />

--<br />

There are 56 types for which we have verified the citations:<br />

most <strong>of</strong> these are holotypes from Clements and Pound. In addition<br />

there are another 80 specimens marked as material on which new<br />

taxa were based that are in the process <strong>of</strong> verification.<br />

Several <strong>of</strong>' Bessev's students and succeeding Nebraska<br />

mycologists made extensive collections <strong>of</strong> fungi from the state.<br />

They are J M.'Bates, F.E Clements, E.E. Dale, N.F. Peterson, R J.<br />

Pool, W.W. Ray, P.A. Rydberg. DeA. Saunders, E.C. Tullis, L.B.<br />

Walker, H.J Webber, and A.F. Woods.


The exchange program begun at +he end <strong>of</strong> the last century was<br />

extensive. Among the North <strong>America</strong>n and European collections re-<br />

presented are C.F. Baker, California and Pacific Slope Fungi: E.<br />

Bartholomew. North <strong>America</strong>n Uredinales and Fungi Columbiana: E.<br />

Bethel, Colorado Flora--Fungi: Brenckle, Fungi Dakotensis, F.E.<br />

and E.S. Clements,-Cryptogamae Formationum Coloradensium: M.A.<br />

Curtis, eastern United States; Ellis, North <strong>America</strong>n Fungi; Ellis<br />

and Everhart, North <strong>America</strong>n Fungi and Fungi Columbiana: W.G.<br />

Farlow; D. Griffiths, West <strong>America</strong>n Fungi; C.A. Hart, Economic<br />

Fungi: E.W. Holway, North <strong>America</strong>n Fungi; W.A. Kellerman, Ohio<br />

Fungi, Kellerman and Swingle, Kansas Fungi; Linhart, Fungi<br />

Hungarici; A. Ludwig, Mycotheca Germanica; G. Oertel, Mycot.heca<br />

Germanica; C.G. Pringle, Arizona: Ravenel, Fungi. Caroliniana: L.<br />

Romell, Fungi Exsiccati Praesertim Scandinavici; A.B. Seymour and<br />

F.S. Earle. Economic Fungi; C.L. Shear,'New York Fungi: E.P.<br />

Sheldon, Plant <strong>of</strong> the Minnesota Valley: Sydow, Mycotheca Germanica<br />

and Ustilagineen; Thumen, Mycotheca Universalis and Herb. Mycol.<br />

Oeconomicum; W. Trelease. North <strong>America</strong>n Fungi; USDA BPI Plant<br />

Disease Survey; University <strong>of</strong> California Herbarium, California<br />

Fungi; Vestergren, Micromycetes Rariores Selecti: and C. Wright.,<br />

Cuba.<br />

CURRENT WORK: FUNGAL ---<br />

CONSERVATION PROJECT<br />

In the fall <strong>of</strong> 1987, Messenger and Bolick tested the pH <strong>of</strong> a<br />

sample <strong>of</strong> the paper packets in which the fungal collections were<br />

held, the sheets on which the packets wee mounted, and the labels.<br />

The pH <strong>of</strong> the packet and mounting papers ranged from 3 to 4.5 and<br />

that <strong>of</strong> the label paper, from 3 to-5. As the survey indicated<br />

that new papers and label deacidification were needed, a grant to<br />

the Institute <strong>of</strong> Museum Services (IMS) Conservation Grant Program<br />

was prepared and submitted.<br />

In August 1988, NEB was not.ified that funding had been<br />

awarded by the IMS. The conservation project was begun in October<br />

1988. Grant funds were used to ourchase new storage cabinet.^ and<br />

acid-free, 100 percent rag paper for new packets. The grant also<br />

provided funds to'bring a paper conservator, Robert A: McCarroll,<br />

from the Rockey Mountain Conservation Center in Denver, Colorado<br />

to teach the staff how to treat the specimens and labels.<br />

The University <strong>of</strong> Nebraska's matching funds for the grant<br />

were used, in part, to purchase the supplies and eaui~ment needed<br />

to establish a basic paper conservation laboratory. Work is now<br />

in progress on repackaging the fungal specimens in acid-free, 100<br />

percent rag packets and deacidifying the specimen labels.<br />

REQUEST - FOR MYCOLOGISTS BORROW SPECIMENS<br />

NEB would like to encourage all mycologists doing revi-<br />

sionary or floristic studies to check with us when planning their<br />

loans. We would be happy to loan you our material and would<br />

appreciate any <strong>of</strong>fers to annotate specimens.<br />

REFERENCE<br />

Payne, W.W., T.B. Croat, M.E. Hale, P.K Holmgren, 9. McVaugh,<br />

1974. Systematic Botany Resources In <strong>America</strong>n, Part I.<br />

Survey and Preliminary Ranking. New York: New York<br />

Botanical Garden. 88p.


Apply now for the<br />

James W. Sinden Scholarship<br />

The James W. Sinden Scholarship Committee <strong>of</strong> the <strong>America</strong>n Mushroom Institute<br />

is pleased to announce the availability <strong>of</strong> a single scholarship <strong>of</strong> up to<br />

$2,500. to be awarded on a yearly basis to a graduate student conducting<br />

dissertation research involving edible mushrooms and/or other edible fungi.<br />

The fund has been established in the name <strong>of</strong> Dr. James Sinden in recognition<br />

<strong>of</strong> his outstanding contributions to the science and industry related to the<br />

commercial mushroom.<br />

Applicants will be accepted until May 1, 1990 after which the Committee reserves<br />

the right <strong>of</strong> refusal. Will need:<br />

.Undergraduate and graduate transcripts;<br />

.Four letters <strong>of</strong> recommendation - two <strong>of</strong> which should be from<br />

persons familiar with your academic record.<br />

.Results <strong>of</strong> the Aptitude Section (quantitative and verbal) <strong>of</strong><br />

the Graduate Record examination. Dates GRE was taken.<br />

.One page statement <strong>of</strong> the thesis research project and career plans.<br />

.Copy <strong>of</strong> application for admittance to University (if available).<br />

.List <strong>of</strong> current scholarships or grants if any to support your<br />

research activities.<br />

Applicants must adhere to financial policies relative to the grant as stated by<br />

the J.W. Sinden Scholarship Committee.<br />

Applications available from:<br />

Dr. James W. Sinden Scholarship Committee<br />

!&erican Mushroom Institute<br />

907 E. Baltimore Pike<br />

Kennett Square, PA 19348<br />

(215) 388-7806<br />

EDITOR'S NOTE: Although the application deadline does not appear<br />

to be an absolute one, it may be too late for applications to be<br />

submitted to the Sinden Scholarship Committee this year.<br />

However, readers can be prepared for future years, and the News-<br />

letter can run a similar notice in the October issue.


THE ALEXANDER H. AND HELEN V. SMITH RESEARCH FUND<br />

The Awards Committee for this fund will be pleased to receive<br />

inquiries and applications regarding the use <strong>of</strong> this fund. Since<br />

the <strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> <strong>America</strong> is meeting the latter part <strong>of</strong><br />

June this year the deadline for receipt <strong>of</strong> applications is May 1,<br />

1989<br />

The primary purpose <strong>of</strong> the fund is to encourage study <strong>of</strong> speci-<br />

mens <strong>of</strong> fungi collected by Alexander H. Smith and his associates.<br />

These collections, and materials relating to them, are currently<br />

deposited at the University <strong>of</strong> Michigan Herbarium. The Fund will<br />

will distribute grants-in-aid to cover all or a significant part<br />

<strong>of</strong> the expense <strong>of</strong> coming to the Herbarium and working with the<br />

collections or materials related to them.<br />

Grants may be made available to members <strong>of</strong> the <strong>Mycological</strong> Socie-<br />

ty <strong>of</strong> <strong>America</strong> who are working actively on the taxonomy or<br />

floristics <strong>of</strong> the fleshy fungi. They should be to a point in<br />

their studies where having full access to Alex's material would<br />

advance the applicant's work. These grants will not be used for<br />

preliminary studies <strong>of</strong> possible lines <strong>of</strong> investigation.<br />

Applications for a grant should include 1) a proposal indicating<br />

how the study <strong>of</strong> Alex's specimens and manuscripts would advance<br />

the applicants work, 2) an estimated budget to cover all or part<br />

<strong>of</strong> the anticipated expenses (e.g., travel, per diem, copying),<br />

and 3) a current curriculum vitae.<br />

Recipients will be chosen by an awards committee designated by<br />

the President <strong>of</strong> the <strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> <strong>America</strong>. In addi-<br />

tion, the agreement <strong>of</strong> the Director <strong>of</strong> the University <strong>of</strong> Michigan<br />

Herbarium to have the potential recipient(s) work there must be<br />

obtained before the grant is awarded.<br />

A copy <strong>of</strong> the complete guidelines or further information may be<br />

obtained from: Harry D. Thiers<br />

Department <strong>of</strong> Biology<br />

San Francisco State University<br />

San Francisco, CA 94132<br />

The <strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> <strong>America</strong> will be pleased to accept<br />

donations to the fund; those interested are urged to send their<br />

contributions to the Treasurer <strong>of</strong> the <strong>Society</strong>.<br />

EDITOR'S NOTE: The date at the end <strong>of</strong> the first paragraph<br />

probably should have been 1990, and the deadline may be past by<br />

the time this issue <strong>of</strong> the Newsletter is received by readers.<br />

However, there is additional information in the notice, and a<br />

similar notice can be prepared for the October issue.


<strong>Mycological</strong> Papers, No. 161<br />

ASPERGILLUS SPECIES ON STORED<br />

PRODUCTS<br />

CAB International <strong>Mycological</strong> Institute, Ferry Lane, Kew, Surrey TW9 3AF, UK<br />

Aspergillus is a major cause <strong>of</strong> deterioration and spoilage amongst a wide range <strong>of</strong> stored<br />

materials,particularly foodstuffs. Many species produce toxins harmful to the consumer, and<br />

exposure to their spores may result in respiratory allergies. Others are employed in the commercial<br />

preparation <strong>of</strong> widely used oriental foods, vitamins, enzymes, antibiotics and industrial acids. Rapid<br />

accurate identification to species in these contexts is essential.<br />

New criteria for species determination based largely upon scanning electron microscope studies <strong>of</strong><br />

spore ornamentation are presented. Isolates associated with stored products, representing 137<br />

Aspergillus taxa in eleven species groups, are included.<br />

Phenotypic variation relative to the environment and genetic backgrounds Is considered. Results are<br />

used to delimit species boundaries, to evaluate the strength <strong>of</strong> traditional characters and to review the<br />

taxonomic status <strong>of</strong> species associated with food and the domestic environment.<br />

Six established varieties are retained as such. Twelve species are reduced to varietal rank and a<br />

further six reduced to synonymy. Six varieties are raised to species rank and another two species re-<br />

established.<br />

Alterations, brought about by revision <strong>of</strong> the ~otanicai'code in 1981, have resulted in name changes<br />

for a number <strong>of</strong> Aspergillus anamorphs, particularly in Eurotium and Neosartorya. Seven name<br />

chan,ges in the A. glaucus and (Eurotium) group, and three in the A. fumigatus group (Neosartorya), are<br />

proposed.<br />

Keys to species are provided, based on traditional characters and on scanning electron microscope<br />

features.<br />

(June 1989) 188 Pages ISBN 0 851 98 632 3<br />

Price including postage:<br />

£30.00 UK US$56.00 <strong>America</strong>s £33.00 Elsewheree


(An. infomtive thrill a page. )) - Li6rary J oud<br />

gfyoujre interested in mushrooms and the<br />

ou~ors, you s f d 6e reading Mushroom,<br />

the youd, 6ecause &is is just a sample gf<br />

wfurt welve already avered:<br />

lssue 1 (Fall 1983) - Artistic Spore Prlnts (Here's how to make them);<br />

Mushrooms at the Summit (Cralg Clalborne shares hls reclpe from<br />

Willlamsburg); What Makes a Good Fleld Gulde? (Nlne <strong>of</strong> those avallable<br />

In 1983 are evaluated)<br />

issue 2 (Wlnter 1983-84) - Toxins end Halluclnogens (The slow-teact<br />

mushrooms are the most deadly); The Woodrotters (Lumbar may coma to<br />

you wlth fungl In place)<br />

lssue 3 (Sprlng 1984) - For the Flrst Tlme (How do you know when to go<br />

out In sprlng?); Keys (An introduction to a vital tool)<br />

lssue 4 (Summer 1984) - NO LONGER AVAILABLE<br />

lssue 5 (Fall 1984) - Growlng Your Own Oysters (It's not difficult to get<br />

started); Mushroom Bandits (You have some tough competltlon out there)<br />

lssue 6 (Winter. 1984-85) - NO LONGER AVAILABLE<br />

lssue 7 (Spring 1985) - The Merkle (Eugene J. McCerthy phllosophlzes);<br />

A Critlque <strong>of</strong> the Photos In the Audubon Fleld Guide (By Gary Llnc<strong>of</strong>f)<br />

issue 8 (Summer 1985) - Key for Use wlth the Audubon Fleld Guide (By<br />

Gary Llnc<strong>of</strong>f); Just for the Smell <strong>of</strong> It (Bringlng your nose into play can help<br />

with Identiflcatlon)<br />

lssue 9 (Fall 1985) - The Inky Caps (Autodlgestion makes them special)<br />

lssue 10 (Wlnter 1985-86) - The Macgruder Statements (Ten Interested<br />

parties comment on overplck); All Klnds <strong>of</strong> Baskets (it's possible to have<br />

many, but never too many)<br />

lssue 21 (Fall, 1988) - Anclent Forests (We need lo save some); To Russla<br />

with Mushrooms; Get Started in Cuitlvatlon by Going to Garage Sales;<br />

issue 11 (Spring 1986)- Find Those Morels (Wlth advlce from the wlnner <strong>of</strong><br />

the national morel-hunting champlonshlp); The 1,2,3.4,5 <strong>of</strong> Starting Out (The<br />

experts come close to agreement on how beginners should proceed)<br />

lssue 12 (Summer 1986) - Controlllng the Mushrooms <strong>of</strong> Norway; Lumplng<br />

and Splltling (There are fewer, or more, species. depending on which camp<br />

you're in)<br />

Where the Yangtse Bends<br />

Issue 22 winter, 1988-89) - A Wlnter Project (Start planning for Sprlng);<br />

Armlllaria Is Blg in Idaho(lt's called root rot); What's Happening wlth Amanita<br />

Phalloides?<br />

Issue 23 (Spring, 1989) - What's Holdlng up Tame Morels? (The patent was<br />

issued a long time ago); Are They Raking Our Truffles to Death? And yes,<br />

Can Own tuber hound<br />

lssue 13 (Fail 1986) - The Chanterelle; Cultlvatlng Morels (wlth detalls <strong>of</strong><br />

the newly-patented process); Should Sale <strong>of</strong> Wlld Mushrooms be Regulated?<br />

(The F wd and Drug Admlnistratlon thinks so)<br />

lssue 14 (Winter 1986-87) - Fungal Allergy; The Big Problem In Alaska is<br />

Underpick (or, maybe, bears); You Can Grow the Garden Glanl In Your -ad &is is ~fi(Lt we'a<br />

Backyard<br />

Issue 15 (Spring 1987) - NO LONGER AVAILABLE<br />

lssue 16 (Summer 1987) - The Chiggers Are Out There (but you can foil<br />

most <strong>of</strong> them); Chuck Barrows Looks Back (and sldeways and to the future)<br />

lssue 17 (Fall 1987) -The Nutrltional Value <strong>of</strong> Mushrooms (It's qulle specles<br />

speclflc); The FDA Issues Its Mushroom Interpretation (and leadlng<br />

rnushrwmers react)<br />

lssue 18 (Winter 1987-88) - The 20 Most Beautiful Mushrooms (wlth no<br />

swimsuit competltlon to complicate thlngs); Early Mushroom Manuals In the<br />

U.S. (One was wrltten by a death-defylng tastetester)<br />

lssue 19 (Sprlng, 1988) - The Definitive WIrd on Mycorrhizae (They're<br />

Important lo more than just mushrooms); Llfe In the Bog; You Can Cook with<br />

Splrlt end Spirlts<br />

lssue 20 (Summer, 1988) - Deadly Humor (How mushroomers joke about<br />

danger); Mushrooms Decllne In 10 European Countrles; Using the Microscope<br />

(An Introduction by Leo Tanghe); Pronounce it Correctly (or be In good<br />

company)<br />

dklive-r in tfie +re:<br />

your satisfizction. @urrante46.<br />

Send check or money order (not a purchase order) to:<br />

Mushroom, Box 31 56, University Station,<br />

Moscow, Idaho 83843<br />

Name:<br />

Address:<br />

Zip Code:<br />

issues (Subscrlptlons are $16 a year for four issues. In Canada, mark<br />

checks "US dollars." Subscriptions have to begin with the next<br />

Issue, but back Issues, If available, can be ordered separately<br />

at $4 each postpald (or three or more at $3 each postpald).<br />

are $4 eucfi postpaid<br />

($3 each for 3 or more)<br />

i


L. F. LAMBERT SPAWN CO., INC. -- Producers <strong>of</strong> edible fungi<br />

cultures and spawn -- P.O. Box 407, Coatesville,<br />

Pennsylvania 19320.<br />

LANE SCIENCE EQUIPMENT CO. -- Complete line <strong>of</strong> mushroom storage<br />

cabinets, especially herbarium cabinets, airtight for<br />

permanent protection -- 225 West 34th Street, Suite 1412,<br />

New York, NY 10122. (212) 563-0663.<br />

MERCK SHARP & DOHME RESEARCH LABORATORIES, Division <strong>of</strong> Merck &<br />

Co., Inc., Rahway, New Jersey 07065.<br />

MILES, INC. -- Pharmaceutical and chemical research and<br />

manufacture -- Elkhart, Indiana 46515.<br />

MYCOTAXON, LTD. -- Publishers <strong>of</strong> Mycotaxon, an international<br />

journal <strong>of</strong> the taxonomy and nomenclature <strong>of</strong> fungi and<br />

lichens -- P.O. Box 264, Ithaca, New York 14851.<br />

TED PELLA INC., PELCO -- Transmission and scanning electron<br />

microscopy instruments and supplies -- P.O. Box 2318,<br />

Redding, California 96099.<br />

PFIZER, INC. -- Fine chemicals and pharmaceuticals by means <strong>of</strong><br />

microorganisms -- 235 East 42nd Street, New York, NY 10017.<br />

(203) 441-4100.<br />

PIONEER HI-BRED INTERNATIONAL, INC. -- World- leader in genetic<br />

research for agriculture -- 7250 NW 62nd Avenue, Johnston,<br />

Iowa 50131. (516-5) 270-4100.<br />

ROHM AND HAAS CO. -- Specialty monomers, polymers, industrial<br />

biocides , and agricultural chemicals -- Research<br />

Laboratories, Spring House, Pennsylvania 19477.<br />

SCHERING CORPORATION -- Pharmaceutical Research & Development --<br />

Orange St., Bloomfield, New Jersey 07003.<br />

SMITHKLINE BEECHAM PHARMACEUTICALS, P.O. Box 7929, Philadelphia,<br />

Pennsylvania 19101.<br />

SPAWN MATE, INC. --- Delayed release nutrient supplements,<br />

research labs and technical service, and products for the<br />

mushroom industry -- P.O. Box 1990, Santa Cruz, CA 95061<br />

TRIARCH INCORPORATED -- Quality prepared microscope slides,<br />

catalog-listed, or custom prepared to your specifications --<br />

Ripon, Wisconsin 54971.<br />

UNIROYAL CHEMICAL COMPANY, INC. -- Producers <strong>of</strong> crop protection/<br />

production chemicals; fungicides, insecticides, miticides,<br />

herbicides, plant growth regulants, and foliar nutrients --<br />

70 Amity Road, Bethany, Connecticut 06525<br />

THE UPJOHN COMPANY -- Pharmaceutical Research and Development --<br />

301 Henrietta Street, Kalamazoo, Michigan 49007.<br />

PHARMACEUTICAL RESEARCH DIVISION, WARNER-LAMBERT COMPANY, 2800<br />

Plymouth Road, Ann Arbor, Michigan 48105


Terrence M. Hammili, Editor<br />

<strong>Mycological</strong> <strong>Society</strong> <strong>of</strong> <strong>America</strong> NEWSLETTER<br />

B-18A Piez Hall<br />

SUNY College at Oswego<br />

Oswego, New York 13126<br />

USA<br />

NONPROFIT ORG.<br />

U.S. POSTAGE<br />

PAID<br />

OSWEGO, NY<br />

PERMIT NO. 317<br />

There are three inserts:<br />

A. The MSA Newsletter Questionnaire (blue)<br />

B. The Employee/Ernployer Data Form (green -- new address for Bob<br />

Pohlad)<br />

C. An MSA Newsletter Survey (yellow)

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