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324<br />

NUCLEAR NUMBER AND BEHAVIOR IN SCLEROTINIA SCLEROTIORUM. E. J.<br />

Ford, D. C. Sands, and K. Adkisson, Dept. of Plant Pathology,<br />

Montana State University, Bozeman, MT 59717.<br />

was only partially effective on strawberry. Both mixtures<br />

increased dicarboximide resistance. Thiram or chlorothalonil<br />

useo alone did not provide satisfactory crey mould control hut<br />

did decrease the incidence of dicarboximide resistant strains.<br />

Fluorescent microscopy was used to study nuclear number and<br />

behavior in asci, ascospores, germinating ascospores, hyphae,<br />

protoplasts and microconidia of S. sclerotiorum. Specimens were<br />

stained with hydroethidine, DAPI, propidium iodide, Hoerst, and<br />

calcofluor either singly or in various combinations to reveal<br />

details of nuclear number, meiosis, mitosis, and cell wall<br />

development. Classical patterns of meiosis were observed in<br />

asci with 8 nuclei being formed followed by wall formation and<br />

then a final nuclear division to yield two nuclei per mature<br />

ascospore. Nuclear division in ascospores was evident after 2<br />

hrs incubation in a nutrient broth at room temperature, which<br />

was prior to germination of the ascospores. Young sporelings<br />

had up to 16 nuclei prior to cross wall formation. A nuclear<br />

generation time of ca. 2.4 hrs was determined for sporelings.<br />

Hyphae from young shake cultures had 20-30 nuclei/cell,<br />

Spheroplasts formed from active hyphae averaged 3.5 nuclei per<br />

spheroplast. Microconidia were uninucleate.<br />

328<br />

HYBRID PERFORMANCE AND YIELD LOSSES ASSOCIATED WITH GRAY LEAF<br />

SPOT DISEASE OF CORN IN VIRGINIA. P. J. Donahue and E. L.<br />

Stromberg, Departments of Agronomy and Plant Pathology, Phy<br />

Strog, departments of Alant PA Phy-<br />

siology and Weed Science, VPI&SU, Blacksburg, VA 24061-0331.<br />

Commercial corn hybrids were evaluated for 7 years at Wythe and<br />

Shenandoah Counties and 1 year at Montgomery Co. under field<br />

conditions for response to gray leaf spot disease, caused by<br />

Cercospora zeae-maydis. Plants were scored 3 times during<br />

the growing season. Disease severity indices were regressed<br />

against grain yield and harvest moisture, and lodging by location<br />

and year. Significant grain loss due to disease occurred in 2<br />

of 6 years at the Shenandoah Co. site and 1 of 6 years at the<br />

Wythe Co. site. A significant increase in lodging occurred in<br />

325<br />

ON HOST FAMILIES AND GENERA OF PERONOSPORA AND PLASBMOPBA<br />

DOWNY MILDEWS AND ON GEOGRAPHIC PROCLIVITIES OF THE PATHOGENS.<br />

R.Kenneth, Hebrew Univ. Fac. of Agric., Rehovot 76100, Israel<br />

2 of 6 years at the Shenandoah Co. site and 5 of 6 years<br />

at the Wythe Co. site. These data represent the effects of C<br />

zeae-maydis<br />

tial.<br />

on a range of genotypes<br />

The<br />

differing in yield poten-<br />

fact that significant associations occurred indicate<br />

the strong effect gray leaf spot can have when environmental<br />

conditions are favorable.<br />

Data from host-downy mildew (dm) check-lists provided information<br />

on the two most common genera of Peronosporaceae. Of the<br />

ca 51 host families with Peronospora, 8 are stricken in single<br />

countries only; of the 22 with Plasmopara, at least 4. Despite<br />

a dearth of dms of these genera in the tropics, a few thrive<br />

e.g. Plasmopara on Vitaceae and Peronospora on Euphorbiaceae,<br />

the latter unrecorded in cold regions. Australia and New<br />

Zealand have few dms: 3 and 10 host families respectively with<br />

PeronosPora and 1 and 2 with Plasmopara (vs 34 in Romania with<br />

Persnoanora and ca 17 in USA and 9 in Canada with Plasmopara).<br />

Although Plasmopara is recorded on only 7 families in Britain<br />

and 8 in France, there are 20 and 26 host genera of Umbelliferae<br />

vs only 4 and 2 in USA and Canada (and none in the east<br />

Mediterranean Basin). For Plasmopara on Asteraceae, however,<br />

there are ca 20 host genera in USA vs none in Britain and 4 in<br />

France. Of the 33 legume genera with Peronosl.ora, 8 are in<br />

single countries only e.g. Cicer in Israel, yigna in USA.<br />

326<br />

SCLEROTINIA BLIGHT OF PEANUT IN TEXAS: OCCURRENCE AND DETECTION<br />

OF THE PATHOGEN IN SEED. R.A. Taber, D.H. Smith, J. S. Neck,<br />

S.L. Segner, D.M. Porter, D.H. Lewis, and T.M. Omran. Dept. 329<br />

Plant Path. & Micro., Unierity tatonandYokum Tx. Cllee Agri. Exp. Sta., T;; Texas SD, AS, A&M EVALU]ATION OF MEIHDSFOR SAMPIG, RIECOVERY<br />

University,<br />

AND<br />

College Station<br />

ENUMERATION<br />

and<br />

OF<br />

Yoakum, Tx.;-USDA, ARS, BAC IA APPLIED TO THE PHYLLOSPHERE. Q. A. MatyacI, K.<br />

Suffolk, Va.; and Vet. Micro., TAMIU, College Station, Tx. 77843 Donegan , R. Seidler 2 , V. Prince 1 and A. Porteus2. N.S.I.<br />

Peanut Sclerotinia blight was first observed in Texas in Mason Technology ServicesI and E.P.A.2, Corvallis Environ.ental<br />

County in 1981 on cv. 'Florunner'. Since 1981 it has been Research Laboratory, Corvallis, OR. 97333.<br />

observed in other counties in Texas. The role of seed in Erwini herbicola or Enterobacter cloacae were sprayed on oa<br />

propagule dispersal is currently under study. Sclerotia were orwin le a Bacteri ac te r oaca e le af a nd bulk<br />

observed in infested seed; however, the incidence was less than or bean leaves. Bacterial Counts from single leaf and bulk<br />

1%. In spite of seed shriveling and discoloration, leaf samples were similar 1-7 days after application, bit after<br />

germinability and emergence from infested seed exceeded 90%. 14-35 days Counts from bilk samples were significantly larger.<br />

Presence of the pathogen was successfully detected in seed Butlk sample values could be adjusted to those of mingle leaves<br />

using the Agri-Diagnostics Inmunoassay Kit and serial using estimates of the single leaf varianc. More bacteria<br />

sectioning. The pathogen was most prevalent in the peanut were remo~ved by stomacher blending than sonication, blending,<br />

testa. Fluorescein isothiocyanate-labeled monoclonal antibodies or washing leaves in biffer. Stomacher blendling was reliable<br />

developed from an isolate of Sclerotinia from Texas peanuts ovrawdrngofbceilppatnsndhn2-0%f<br />

permitted localization and verification of specific hyphae of t)he Leaf sample carried bacteria. The surface drop technique<br />

the pathogen in the seed with the aid of immunofluorescence, f~r enumerzation of bacteria uses four 10 ul aliquots and showed<br />

nO cifferene from the 100 ul aliquot spread plate method.<br />

,These methods proved to be rapid, efficient and precise in<br />

327 estimating parametera of bacterial populations.<br />

INFLUENCE OF SPRAY SCHEDULES O)N RESIST/GIT POPULATIONiS OF BOTRY-<br />

TIS CINEREA. M.L. GULLINC, C. ALDI and A. GARIBALDI Istituto di 330<br />

Patologia vegetale, Via Giuria 15, 10126 Torino, Italy.<br />

In the presence of benziinidazole and dicarboximide resistant<br />

strans cnera f Btryts Pes. nd f hih dseae inidece,<br />

treatm~ents with di carboximides provided only partial control of<br />

grey mould on grape, strawberry and tomato and increased the<br />

percent of dicarboximide resistant strains. The combination of<br />

a benzimidazole with diethofencarb (alternated or not with a<br />

dicaooxinie) dicaboxmid) stisactry<br />

atifactry povied<br />

oovied ontol<br />

ontol o<br />

f<br />

gry<br />

gry<br />

muldand<br />

muldand<br />

decreased the percent of benzimidazole resistant strains. The<br />

mixture of procysidone with thiran controlled grey mould of<br />

grape, while the combination of orocymidone and chlorothalonil<br />

DIFFERENTIATION OF TOMATO RACES 1 AND 2 OF VERTICILLIUM DAHLIAE<br />

USING VEGETATIVE COMPATIBILITY ANALYSIS. T. R. Joaauim and R.<br />

C. Rowe, Dept. of Plant Pathology and W. A. Erb, Dept. of<br />

HriutrOi tt nvWotr H461<br />

Sixteen strains of Verticillium dahliae, designated as either<br />

tomato races 1 or 2, were tested for vegetative compatibility.<br />

Compatibility was assessed by pairing complementary, nitrate-<br />

mutants<br />

nonutilizing<br />

of tester<br />

(nit)<br />

strains<br />

mutants<br />

representing<br />

derived from each<br />

several<br />

strain with<br />

vegetative<br />

nit<br />

compatibility groups (VCGs) (Phytopathology 73:1305-1308). Nit<br />

mutants were isolated from each wild-type strain by selecting<br />

for chlorate resistance on corn meal agar with dextrose (Difco)<br />

1176 PHYTOPATHOLOGY

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