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Inoculum 56(4) - Mycological Society of America

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MSA ABSTRACTS<br />

Mayor, Jordan R. 1 *, Henkel, Terry W. 1 and Aime, M. Catherine 2 . 1 Department <strong>of</strong><br />

Biological Sciences, Humboldt State University, Arcata, CA 95521, USA,<br />

2 USDA-ARS, Systematic Botany and Mycology Lab, Beltsville, Maryland<br />

20705, USA. jrm46@humboldt.edu. Ectomycorrhizae accelerate calcium acquisition<br />

from leaf litter in a monodominant Dicymbe corymbosa (Caesalpiniaceae)<br />

forest in Guyana.<br />

We tested the hypothesis that ectomycorrhizae (EM) alter mineral nutrient<br />

concentrations and decomposition <strong>of</strong> leaf litter within a monodominant forest <strong>of</strong><br />

the ectomycorrhizal, canopy tree Dicymbe corymbosa Spruce ex Benth. in<br />

Guyana. A root-exclusion experiment and a reciprocal transplant experiment were<br />

performed to determine how the exclusion <strong>of</strong> ectomycorrhizae would influence<br />

decomposition <strong>of</strong> D. corymbosa leaves. Mass loss <strong>of</strong> D. corymbosa leaf litter was<br />

determined on three occasions during a 12 month period, and was unaffected by<br />

the presence <strong>of</strong> ectomycorrhizae. Elemental analysis <strong>of</strong> N, P, K, Ca, and Mg was<br />

performed on the residual D. corymbosa leaf litter after 12 months. Both experiments<br />

demonstrated that, at 12 months, leaf litter Ca concentrations were significantly<br />

reduced in the presence <strong>of</strong> ectomycorrhizae. These results suggested an ectomycorrhizal<br />

enzymatic mode <strong>of</strong> Ca mobilization which may facilitate continued<br />

root growth and domination <strong>of</strong> litter layers by ectomycorrhizae. Additionally,<br />

saprotrophic fungi that specialize on Dicymbe leaves have been identified through<br />

multi-year plot sampling; these foliicolous specialists may facilitate rapid decomposition<br />

<strong>of</strong> D. corymbosa leaves within monodominant forests and, in conjunction<br />

with ectomycorrhizae, contribute to rapid mineral nutrient recycling in the<br />

system. poster<br />

McAlpin, Cesaria E. and *Wicklow, Donald T. USDA, ARS, National Center for<br />

Agricultural Utilization Research, Peoria IL, USA. wicklodt@ncaur.usda.gov.<br />

DNA fingerprinting analysis <strong>of</strong> Petromyces alliaceus section Flavi.<br />

The objective <strong>of</strong> this study was to evaluate the Aspergillus flavus pAF28<br />

DNA probe’s ability to produce DNA fingerprints for distinguishing among genotypes<br />

<strong>of</strong> Petromyces alliaceus section Flavi, a fungus considered responsible for<br />

the ochratoxin A contamination that is occasionally observed in California fig orchards.<br />

Petromyces alliaceus, P. albertensis and 7 species in Aspergillus section<br />

Circumdati were analyzed by DNA fingerprinting using a repetitive sequence<br />

DNA probe pAF28 derived from A. flavus. The presence <strong>of</strong> hybridization bands<br />

with the DNA probe and the P. alliaceus or P. albertensis genomic DNA indicates<br />

a close relationship between A. flavus and Petromyces alliaceus section<br />

Flavi. Twelve distinct DNA fingerprint groups or genotypes were identified<br />

among 15 isolates <strong>of</strong> Petromyces. Species belonging to Aspergillus section Circumdati<br />

hybridized only slightly at the 7.0 kb region with the repetitive DNA<br />

probe, suggesting very little DNA homology. The pAF28 DNA probe <strong>of</strong>fers a<br />

tool for typing and monitoring specific P. alliaceus clonal populations and for estimating<br />

the genotypic diversity <strong>of</strong> P. alliaceus in orchards, vinyards or crop<br />

fields. poster<br />

McKay, Doni 1 *, Jennings, Tara 2 and Smith, Jane E. 1 . 1 USDA Forest Service, Pacific<br />

Northwest Research Station, Corvallis, OR 97331, USA, 2 Department <strong>of</strong><br />

Forest Science, Oregon State University, Corvallis, OR 97331, USA. dmckay@fs.fed.us.<br />

Life in red soils: Investigating forest recovery after wildfire.<br />

Post-fire forest recovery is dependent on functioning soil fungal communities.<br />

To examine effects <strong>of</strong> burn severity on soil recovery we are measuring total<br />

fungal diversity and nutrients from soil from the 2003 Booth & Bear Butte fire<br />

complex in the Cascade Range <strong>of</strong> Oregon. Soil samples were collected immediately<br />

after fire and 3 times during the post-fire year from 24 paired plots <strong>of</strong> detrimentally<br />

(severely) and moderately burned soils. Using TRFLP techniques, we<br />

show that soil fungal diversity is low for the detrimentally burned soils and typically<br />

higher in the moderately burned soils. The detrimentally burned soils were<br />

higher in pH than the moderately burned soils, whereas the moderately burned<br />

soils had higher measures <strong>of</strong> ammonium, nitrate, carbon, total nitrogen and phosphorous,<br />

and CEC. Soils were also collected for a microcosm seedling bioassay.<br />

Roots were assessed for percent colonization <strong>of</strong> dark septate and ectomycorrhizal<br />

fungi (EMF); molecular PCR methods were used to identify EMF and assess fungal<br />

community recovery. Our results show that fires resulting in large areas <strong>of</strong><br />

detrimentally burned soil decrease nutrient availability, reduce mycorrhizal colonization<br />

<strong>of</strong> regenerating seedlings, and negatively impact post-fire site productivity.<br />

poster<br />

McLaughlin, David J. Dept. <strong>of</strong> Plant Biology, University <strong>of</strong> Minnesota, St. Paul,<br />

MN 55108, USA. davem@umn.edu. The Advance <strong>of</strong> the Basidiomycota: The<br />

View across the Plasma Membrane<br />

During the last 50 years there have been remarkable advances in our knowledge<br />

<strong>of</strong> evolution within the Basidiomycota, new concepts <strong>of</strong> the basidium and<br />

basidiospore release, and an expansion in both taxonomic and structural diversity.<br />

But we remain a long way from a complete understanding <strong>of</strong> evolutionary relationships<br />

within the phylum, and further still from a full elucidation <strong>of</strong> basidiomycete<br />

structure and its functional significance. This review <strong>of</strong> subcellular<br />

structure will begin with the basidium and ballistosporic mechanism. Subcellular<br />

characters have aided us in establishing monophyletic classes, and have been used<br />

to assess relationships between the Ascomycota and Basidiomycota. I will discuss<br />

the latter by reviewing the origin <strong>of</strong> the Uredinales, mitosis in ascomycetous and<br />

40 <strong>Inoculum</strong> <strong>56</strong>(4), August 2005<br />

basidiomycetous yeasts, and Woronin bodies. The availability <strong>of</strong> molecular sequence<br />

data in the 1990’s made possible genetic assessment <strong>of</strong> phylogenies, provided<br />

guidance on interpretation <strong>of</strong> subcellular characters, and made possible the<br />

integration <strong>of</strong> molecular and subcellular characters in phylogenetic analysis. Now<br />

the development <strong>of</strong> bioinformatic databases <strong>of</strong> both molecular and structural characters<br />

will permit the analysis <strong>of</strong> ever larger data sets. These databases also reveal<br />

the scarcity and incompleteness <strong>of</strong> structural studies and provide guidance in filling<br />

gaps in the data. I will consider cystidia as an example <strong>of</strong> understudied structures<br />

with potential phylogenetic utility. In analyzing the Basidiomycota both evolutionary<br />

and cell biologists need to look across the plasma membrane, the former<br />

to understand the implications <strong>of</strong> cell diversity for explaining organismal function,<br />

and the latter to recognize the value <strong>of</strong> comparative studies in understanding cell<br />

function. MSA Presidential Address<br />

McLenon, Terri 1 *, Skillman, Jane 1 , Taylor, Jonathan 1 , Provart, Nicholas 1 and<br />

Moncalvo, Jean-Marc 1,2 . 1 University <strong>of</strong> Toronto, Department <strong>of</strong> Botany, 25 Willcocks<br />

Street, Toronto, ON M5S 3B2, Canada, 2 Royal Ontario Museum, Department<br />

<strong>of</strong> Natural History, Mycology, 100 Queens Park, Toronto, ON M5S 2C6,<br />

Canada. terri.mclenon@utoronto.ca. Documenting fungal communities in soil:<br />

DNA sampling strategies and development <strong>of</strong> bioinformatic tools for automated<br />

phylogenetic identification.<br />

We have compared bulked and point sampling methods for assessing fungal<br />

diversity and community structure in coniferous forest soil from southern Ontario.<br />

Ten nLSU clone libraries were generated to produce at least 50 sequences<br />

per library for a total <strong>of</strong> ca. 800 sequences. Similar sequencing effort recovered a<br />

greater number <strong>of</strong> distinct nLSU sequences from bulked sampling than from point<br />

sampling; however, similar phylogenetic groups were recovered from each library,<br />

although with very little species overlap. Sampling curves did not show any<br />

sign <strong>of</strong> saturation after sequencing 148 clones from a single PCR amplification<br />

nor when all the data were pooled together. Overall, our results suggest that while<br />

a vast sequencing effort is needed to fully document the community <strong>of</strong> fungi in a<br />

forest plot, limited sequencing efforts may be sufficient to quickly document the<br />

presence <strong>of</strong> dominant phylogenetic and ecological groups in a soil horizon at a<br />

given time. We present the prototype <strong>of</strong> a novel bioinformatic tool (FungID) that<br />

addresses some <strong>of</strong> the known difficulties with these types <strong>of</strong> analyses by automatically<br />

integrating an unknown sequence and its top BLAST hits into their corresponding<br />

clade in the fungal tree <strong>of</strong> life. We also discuss how phylogeneticallybased<br />

comparative methods may overcome problems associated with species (or<br />

OTU) circumscription. symposium presentation<br />

Medina, Cristina 1,2 *, González, María C. 1 , Cifuentes, Joaquín 2 , Vidal,<br />

Guadalupe 2 , Sierra, Sigfrido 2 and Medina, Pedro 3 . 1 Universidad Nal. Aut. México,<br />

Instituto de Biología, Depto. Botánica, México, DF 04510, México, 2 Secc.<br />

Micología, Herbario FCME, Facultad de Ciencias, México DF 04510, México,<br />

3 Univ. de Guadalajara, Centro Univ. de la Costa, Depto. Ciencias, Puerto Vallarta,<br />

Jalisco, CP 48280, Mexico. mcgv@ibiologia.unam.mx. Preliminary study <strong>of</strong><br />

gorgonian fungi from Marietas Islands coral reef, Mexico.<br />

Some microscopic fungi associated with Gorgonia sp. from Marietas Islands<br />

coral reef are reported. The mycota associated with coral reef ecosystems<br />

has been little explored and only few studies have been conducted about fungi associated<br />

with pathogenic disease symptoms in various host organisms, usually in<br />

the form <strong>of</strong> tissue necrosis or biomineralisation. Fungi have been observed inhabiting<br />

several coral species including gogonians in the Caribbean and South Pacific.<br />

A sample <strong>of</strong> Gorgonia sp. was collected via SCUBA from Burbuja Cave.<br />

Each sample was placed wet into a sterile plastic bag and transported to the laboratory.<br />

Sections <strong>of</strong> 0.5 square cm were excised from each sample unit. Cut sections<br />

(4 per plate) were surface-sterilised and then were placed onto Petri dishes<br />

containing selective media prepared with sea water with added antibiotics to diminish<br />

bacterial contamination. The inoculated plates were incubated 15 d at<br />

room temperature and with ambient light and each plate was checked daily for the<br />

emergence <strong>of</strong> fungal hyphae, which were transferred to fresh media and purified.<br />

The fungal isolates were grouped according to10 morphological characters and<br />

then each distinctive isolate was chosen for taxonomic identification. Some<br />

recorded fungi were Aspergillus, Cladosporium, Epiccocum, Paecilomyces and<br />

Penicillium. poster<br />

Miadlikowska, Jolanta 1 *, Arnold, A. Elizabeth 2 , Higgins, K. Lindsay 1 , Sarvate,<br />

Senehal 3 , Gugger, Paul 4 , Way, Amanda 1 , H<strong>of</strong>stetter, Valérie 1 and Lutzoni,<br />

François 1 . 1 Duke University, Durham, NC, USA, 2 University <strong>of</strong> Arizona, Tucson,<br />

AZ, USA, 3 University <strong>of</strong> Virginia Health System, Charlottesville, VA, USA,<br />

4 University <strong>of</strong> Minnesota, St. Paul, MN, USA. jolantam@duke.edu. Endolichenic<br />

fungi: random inhabitants or symbiotic partners.<br />

Studies <strong>of</strong> lichenicolous fungi (secondary fungi associated with lichen thalli)<br />

have been restricted, almost exclusively, to fungal species with visible reproductive<br />

structures on lichen surfaces. These visible fungi are abundant in nature<br />

and taxonomically diverse. However, the potential for fungi to occur asymptomatically<br />

within thalli (i.e., as endolichenic fungi, analogous to endophytes <strong>of</strong><br />

plants) remains mostly unexplored. We used a gradient <strong>of</strong> surface-sterilization to<br />

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