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March 2008 - Mycological Society of America

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and Cordycepioideus. This suggests <strong>of</strong> a polyphyletic nature <strong>of</strong> the<br />

genus. In Thailand Ophiocordyceps species linked with Hirsutella<br />

anamorphs are O. unilateralis, O. brunneapunctata, O.communis, O.<br />

humbertii, O. cf. acicularis and O. rhizoidea. Of these six teleomorphs,<br />

only two were formally linked to Hirsutella anamorphs (O. unilateralis<br />

– H. formicarum and O. humbertii – H. saussurei) although on the host<br />

Hirsutella anamorphs have been identified. Molecular work has shown<br />

the close relationship <strong>of</strong> Hymenostilbe and Hirsutella and there are<br />

species sharing features <strong>of</strong> these two genera in their morphology. Our<br />

results show that the genus Hymenostilbe is derived from Hirsutella,<br />

occupying more the upper branches in the tree infecting dipteran flies<br />

to wasps and ants. Contributed Presentation<br />

Manoch, L.*, Jeamjitt, O., Dethoup, T., Eamvijarn, A. and Pikulklin, S.<br />

Department <strong>of</strong> Plant Pathology, Faculty <strong>of</strong> Agriculture, Kasetsart University,<br />

Bangkok 10900, Thailand. agrlkm@ku.ac.th. Some noteworthy<br />

ascomycetes from soil and plants in Thailand. During the course<br />

<strong>of</strong> an ecological survey on the ascomycetes <strong>of</strong> Thailand, soil samples<br />

and diseased plants were collected from various locations. Alcohol and<br />

heat treatments, soil plate, dilution plate methods and Gochenaur’s glucose<br />

ammonium nitrate agar were used to isolate soil fungi. The supplement<br />

<strong>of</strong> actidione (cyclohexemide) to agar media was employed to<br />

isolate keratinolytic fungi. The tissue transplanting technique and half<br />

strength potato dextrose agar (PDA) were employed for isolation <strong>of</strong><br />

plant parasitic fungi from diseased tissues. Morphological characteristics<br />

<strong>of</strong> the ascomycetes were determined, such as growth rate, color,<br />

texture on different agar medium. Microscopic characters were examined<br />

under stereo, light and scanning electron microscopes. The results<br />

revealed that a number <strong>of</strong> Pyrenomycetes were found from soil including<br />

Echinopodospora spinosa, Gelasinospora dictyophora, G. hippopotomata,<br />

Nectria viridescense with Acremonium anamorphic state,<br />

Neurospora africana and N. dodgei. Species <strong>of</strong> Eurotiales (Trichocomaceae)<br />

from soil included Emericella rugulosa, E. variecolor, Eupenicillium<br />

spp., Eurotium spp., Hamigera avellanea, and Talaromyces<br />

spp. Several species <strong>of</strong> keratinolytic fungi were found<br />

including Arachniotus sp. and related genera. Pyrenomycetes from diseased<br />

plants were Nectria hematococca with Fusarium solani anamorphic<br />

state (blight <strong>of</strong> orchid leaf), Gnomonia sp. on cinnamon leaf, Leptosphaerulina<br />

sp. with Phoma sp. anamorphic state (blight <strong>of</strong> cabbage),<br />

and one unidentified species <strong>of</strong> Pyrenomycetes on decaying Ficus twig.<br />

Pure cultures <strong>of</strong> all fungal isolates are being maintained at the Fungal<br />

Culture Collection at the Department <strong>of</strong> Plant Pathology, Kasetsart<br />

University for further investigations. Poster<br />

Mata, Juan L. 1 * and Ovrebo, Clark L. 21 Dept. <strong>of</strong> Biological Sciences,<br />

University <strong>of</strong> South Alabama, Mobile, AL 36695, USA, 2 Dept. <strong>of</strong> Biology,<br />

University <strong>of</strong> Central Oklahoma, Edmond, OK 73034, USA.<br />

jmata@usouthal.edu. New reports <strong>of</strong> Gymnopus for Costa Rica and<br />

Panama. Field trips to the Caribbean lowlands <strong>of</strong> Costa Rica and Panama<br />

in the last two decades have yielded several dozen collybioid collections.<br />

Morphological examination <strong>of</strong> those collections has resulted<br />

in the discovery <strong>of</strong> species not previously reported for this region <strong>of</strong><br />

Central <strong>America</strong>. The distribution range for Gymnopus luxurians, initially<br />

described from southern United States and recently reported in<br />

Dominican Republic, is extended into the Caribbean lowlands <strong>of</strong> Costa<br />

Rica and Panama. Similarly, G. subpruinosus, known from the Greater<br />

Antilles, is reported for Panama. Other new reports for Panama, but<br />

previously recorded from Costa Rica, are G. neotropicus, G. omphalodes,<br />

G. subcyathiformis, and G. luxurians var. copeyi. Poster<br />

Matheny, P. Brandon 1 *, Aime, M. Catherine 2 , Buyck, Bart 3 , Desjardin,<br />

Dennis E. 4 , Horak, Egon 5 and Lodge, D. Jean. 61 Biology Department,<br />

Clark University, 950 Main St., Worcester, Massachusetts 01610,<br />

USA, 2 USDA-ARS, Systematic Botany and Mycology Laboratory,<br />

Room 304, Building 011A, 10300 Baltimore Ave, Beltsville, Maryland<br />

20705-2350, USA, 3 Museum National D’histoire Naturelle, Départment<br />

Systématique et Evolution, Bâtiment de Cryptogamie, Herbier de<br />

Mycologie, Case postale 39 – 57, rue Cuvier, 75231 Paris Cedex 05,<br />

France, 4 Department <strong>of</strong> Biology, San Francisco State University, San<br />

28 Inoculum 59(2), <strong>March</strong> <strong>2008</strong><br />

Francisco, California 94132, USA, 5 Ex-Curator Cryptogamic Herbarium<br />

ZT, Federal Institute <strong>of</strong> Technology, ETH, CH-8092 Zurich,<br />

Switzerland, 6 International Institute <strong>of</strong> Tropical Forestry, USDA Forest<br />

Service-FPL, PO Box 1377 Luqillo, Puerto Rico 00773-1377. pmatheny@clarku.edu.<br />

The evolution <strong>of</strong> tropical species <strong>of</strong> Inocybaceae<br />

(Agaricales). Neotropical and paleotropical species <strong>of</strong> the ectomycorrhizal<br />

(EM) mushroom family Inocybaceae currently comprise 18 percent<br />

<strong>of</strong> the species-level diversity in the family from tropical latitudes,<br />

including lowland and montane habitats. This poor representation <strong>of</strong><br />

tropical taxa, combined with the assumption that morphological traits<br />

<strong>of</strong> tropical species are advanced, suggests that tropical taxa may be recently<br />

derived, and that the family as a whole had a temperate Northern<br />

or Southern hemisphere ancestral area (center <strong>of</strong> origin). As a consequence,<br />

species <strong>of</strong> Inocybaceae are thought to have migrated or<br />

dispersed relatively recently into tropical areas. A corollary <strong>of</strong> these hypotheses<br />

would suggest the EM symbiosis has switched repeatedly to<br />

tropical angiosperm partners <strong>of</strong> Casuarinaceae, Fabaceae, Fagaceae,<br />

Dipterocarpaceae, Myrtaceae, Polygonaceae, Uapacaceae, and perhaps<br />

other partners from temperate gymnosperm and angiosperm partners.<br />

Our recent research has uncovered multiple novel lineages <strong>of</strong> Inocybaceae,<br />

almost all <strong>of</strong> which likely contain endemic undescribed species<br />

from tropical latitudes. In particular, the diversity <strong>of</strong> the family has been<br />

undersampled in Miombo woodlands <strong>of</strong> Zambia, mixed dipterocarp/Fagaceae<br />

forests <strong>of</strong> Thailand and India, and in the neotropics. We<br />

test these hypotheses in a phylogenetic context using a molecular<br />

dataset <strong>of</strong> multiple nuclear genes. We report that tropical taxa <strong>of</strong> Inocybaceae<br />

tend to be diffuse (polyphyletic) throughout the family phylogeny,<br />

and that tropical clades represent both early diverging and recently<br />

derived lineages. Poster<br />

McDonald, Tami R.*, Armaleo, Daniele and Lutzoni, François. Department<br />

<strong>of</strong> Biology, Duke University, Durham, North Carolina, USA.<br />

trm5@duke.edu. Epigenetics <strong>of</strong> the lichen symbiosis. DNA methylation<br />

is a key regulator <strong>of</strong> development in higher eukaryotes. Although<br />

present at negligible levels in many fungi, DNA methylation is considerably<br />

higher in lichen-forming fungi. In the lichen Cladonia grayi, the<br />

DNA <strong>of</strong> the aposymbiotically grown fungus is relatively unmethylated,<br />

while the DNA <strong>of</strong> the fungus in symbiotic association with its algal<br />

partner is highly methylated. As DNA methylation is one hallmark <strong>of</strong><br />

epigenetic gene silencing, this observation suggests that gene silencing<br />

may be a critical step in the formation or maintenance <strong>of</strong> the lichen<br />

symbiosis. To determine which sequences are subject to methylation,<br />

we made a library <strong>of</strong> methylated DNA from the fungal component <strong>of</strong><br />

the lichen. Analysis <strong>of</strong> clones from the library suggests that most targets<br />

<strong>of</strong> DNA methylation are protein-coding sequences rather than intergenic<br />

regions, transposable elements or repeated DNA. The implication<br />

is that these regions are downregulated or silenced in the<br />

symbiotic state. The correlation between DNA methylation on these<br />

candidate regions and the presence <strong>of</strong> related marks <strong>of</strong> epigenetic silencing,<br />

including trancriptionally repressive histone H3 methylation,<br />

presence <strong>of</strong> linker histone H1 and heterochromatin binding protein are<br />

being investigated. Poster<br />

McLenon-Porter, Teresita 1 *, Skillman, Jane E. 1 and Moncalvo, Jean<br />

Marc. 1, 2 1 Department <strong>of</strong> Ecology and Evolutionary Biology, University<br />

<strong>of</strong> Toronto, 25 Willcocks Street, Toronto, ON M5S 3B2, 2 Department<br />

<strong>of</strong> Natural History, Royal Ontario Museum, 100 Queens Park,<br />

Toronto, ON M5S 2C6. terri.mclenon@utoronto.ca. Application <strong>of</strong><br />

phylogenetic methods to assess fungal diversity and community<br />

structure from DNA sequences. Advances in molecular biology techniques,<br />

expansion <strong>of</strong> nucleotide sequence databases, and development<br />

<strong>of</strong> novel bioinformatic tools are collectively making large DNA-based<br />

environmental microbial surveys more common. These methods routinely<br />

detect hundreds <strong>of</strong> divergent sequences from even small halfgram<br />

samples <strong>of</strong> soil that are <strong>of</strong>ten difficult to identify because they<br />

poorly match sequences <strong>of</strong> known taxa in public databases. Phylogenetic<br />

methods can be used to classify unknown sequences, detect new<br />

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