s - Mycological Society of America
s - Mycological Society of America
s - Mycological Society of America
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
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)