Inoculum 56(4) - Mycological Society of America
Inoculum 56(4) - Mycological Society of America
Inoculum 56(4) - Mycological Society of America
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Maryland 20705, USA, 3 1089 A Street, Arcata, California 95521, USA,<br />
4 Kanawapai Village, Upper I, Guyana. twh5@humboldt.edu. Edible mushrooms<br />
used by the Patamona Amerindians <strong>of</strong> Guyana.<br />
Mushrooms are a seasonally important food for the indigenous Patamona<br />
Amerindians <strong>of</strong> the rain-forested Pakaraima Mountains <strong>of</strong> Guyana. In collaboration<br />
with the Patamona, we have documented at least 17 species <strong>of</strong> edible fleshy<br />
fungi. The majority <strong>of</strong> these fungi are undescribed species, and many are ectomycorrhizal<br />
associates <strong>of</strong> leguminous Dicymbe spp. (Caesalpiniaceae). A number<br />
<strong>of</strong> these fungi belong to groups that are infrequently collected for the table by<br />
North <strong>America</strong>ns (e.g., Clavulinaceae, Sarcoscyphaceae, Amanitaceae) whereas<br />
groups which contain highly prized culinary mushrooms by north temperate standards<br />
(e.g., Cantharellaceae) are shunned by the Patamona. The Patamona have<br />
incorporated mushrooms into their pantheon <strong>of</strong> edible wild foods. The breadth <strong>of</strong><br />
wild organisms in other taxonomic groups (e.g. vertebrates, invertebrates, plants)<br />
used by the subsistence Patamona is wide, and mushrooms appear to play a seasonally<br />
important dietary role. Ectomycorrhizal fungi associated with regionallyrestricted<br />
Dicymbe spp. present a unique fungal resource to the Patamona, previously<br />
unrecorded in Amazonian ethnomycology. The fact that not all locally<br />
available edible mushrooms are utilized by the Patamona may reflect the evolving<br />
state <strong>of</strong> their knowledge regarding mushrooms, in which known edible species<br />
are condoned and others remain unknown, and therefore taboo. poster<br />
Henkel, Terry W. 1 *, James, Tim Y. 2 , Miller, Steven L. 3 , Aime, M. Catherine 4 and<br />
Miller, Orson K., Jr. 5 1 Department <strong>of</strong> Biological Sciences, Humboldt State University,<br />
Arcata, CA 95521, USA, 2 Department <strong>of</strong> Biology, Duke University,<br />
Durham, NC 27708, USA, 3 Department <strong>of</strong> Botany, University <strong>of</strong> Wyoming,<br />
Laramie, WY, USA, 4 USDA-ARS, Systematic Botany and Mycology Lab,<br />
Beltsville, MD, USA, 5 Virginia Polytechnic & St. University, P.O. Box 858, Mc-<br />
Call ID 83638, USA. twh5@humboldt.edu. The mycorrhizal status <strong>of</strong> Pseudotulostoma<br />
volvata (Elaphomycetaceae, Eurotiales, Ascomycota).<br />
Pseudotulostoma volvata O.K. Mill. & T. W. Henkel is a morphologically<br />
unusual member <strong>of</strong> the otherwise hypogeous Elaphomycetaceae due to its epigeous<br />
habit, and its spore-bearing mazaedium borne on an elevated stalk at maturity.<br />
Field observations and plot studies in Guyana indicated that P. volvata was<br />
restricted to tropical rain forests dominated by ectomycorrhizal (EM) Dicymbe<br />
corymbosa Spruce ex Benth. (Caesalpiniaceae), suggesting an EM nutritional<br />
mode for the fungus. An EM status for P. volvata would corroborate its placement<br />
in the ectotrophic Elaphomycetaceae. Here we confirm the EM status <strong>of</strong> P. volvata<br />
with a combination <strong>of</strong> morphological, molecular, and mycosociological data.<br />
contributed presentation<br />
Herrera, Jose*, Omodon, Melvin E. and Dillavou, Clayton. Division <strong>of</strong> Science, 100<br />
E. Normal, Truman State University, Kirksville, MO 63501, USA. jherrera@truman.edu.<br />
Assessment <strong>of</strong> fungal infection on borate-treated cellulose insulation.<br />
Cellulose insulation has rapidly gained a large market share among home<br />
builders and buyers. Recent concern regarding health effects <strong>of</strong> high concentrations<br />
<strong>of</strong> fungi within indoor environments (“sick building syndrome”) has promoted<br />
concern about susceptibility <strong>of</strong> building materials including wood products<br />
(in general), and cellulose insulation (specifically) to fungal attack. This study reports<br />
a decrease or absence <strong>of</strong> fungal infection in cellulose insulation made from<br />
recycled paper and treated with varying concentrations <strong>of</strong> sodium polyborate<br />
(Boron 10TM; CAS # 183290-63-3) within ?-scale wall units exposed to variable<br />
and high ambient temperatures and relative humidities throughout the summer.<br />
Our results suggest that cellulose insulation treated with sodium polyborate almost<br />
completely eliminated five common fungal species sprayed onto cellulose<br />
within the wall units and is likely having a cytotoxic or sporocidal effect on many,<br />
if not all, fungal species. These results suggest that cellulose insulation treated<br />
with sodium polyborate, when properly applied and installed, is resistant to fungal<br />
infection for at least 124d at high temperatures and relative humidities. poster<br />
Hibbett, David S.* and Costanzo, Janine. Biology Department, Clark University,<br />
Worcester MA 01610, USA. dhibbett@black.clarku.edu. Measuring fungal discovery:<br />
a survey <strong>of</strong> recent progress in the homobasidiomycetes.<br />
Fungal systematists face the daunting challenge <strong>of</strong> describing all the species<br />
<strong>of</strong> the Mycota on Earth. Fungal ecologists have traditionally been consumers <strong>of</strong><br />
taxonomic research, which provides them with tools for identification. In recent<br />
years, however, fungal molecular ecologists have started to make their own unique<br />
contributions to the discovery <strong>of</strong> biodiversity. We are surveying depositions <strong>of</strong> ITS<br />
and nuc-lsu rDNA sequences <strong>of</strong> homobasidiomycetes to GenBank in an attempt to<br />
quantify the acquisition <strong>of</strong> sequences, and the contribution <strong>of</strong> environmental studies<br />
to the discovery <strong>of</strong> new species. There are about 8000 homobasidiomycete ITS<br />
sequences in GenBank, <strong>of</strong> which 96% were deposited since 1998. In 2004, about<br />
660 ITS sequences <strong>of</strong> homobasidiomycetes were deposited, and 11% <strong>of</strong> these were<br />
from environmental studies. About 10% <strong>of</strong> the environmental sequences were less<br />
than 90% identical to sequences that were in GenBank at the time that they were<br />
deposited. Data for nuc-lsu rDNA are comparable. To complete the catalog <strong>of</strong> extant<br />
fungal diversity, it will be necessary to integrate the data emerging from environmental<br />
studies with those produced by traditional taxonomy. This will require<br />
new phyloinformatics tools, as well as changed attitudes about the requirements for<br />
species description. contributed presentation<br />
MSA ABSTRACTS<br />
Higgins, K. Lindsay 1 *, Arnold, A. Elizabeth 1,2 , Miadlikowska, Jolanta 1 and Lutzoni,<br />
François 1 . 1 Department <strong>of</strong> Biology, Duke University, Durham, NC 27708,<br />
USA 2 Division <strong>of</strong> Plant Pathology and Microbiology, Department <strong>of</strong> Plant Sciences,<br />
University <strong>of</strong> Arizona, Tucson, AZ 85721, USA. klh15@duke.edu. Diversity,<br />
species composition, and evolution <strong>of</strong> fungal endophytes across three<br />
major plant lineages.<br />
Although associated with all plants, fungal endophytes represent an unknown<br />
proportion <strong>of</strong> fungal diversity, and little is known about the phylogenetic<br />
affinity <strong>of</strong> these symbiotic micr<strong>of</strong>ungi. To date, most surveys <strong>of</strong> endophytes associated<br />
with foliage have focused on the temperate zone, such that boreal and<br />
arctic endophytes are poorly known. We used a culture-based approach to survey<br />
endophytic fungi from healthy photosynthetic tissues <strong>of</strong> three host species (Huperzia<br />
sp., Picea mariana, and Dryas octopetala) representing three major lineages<br />
<strong>of</strong> land plants (lycophytes, conifers, and angiosperms, respectively) in boreal<br />
and arctic sites. Phylogenetic analyses <strong>of</strong> the nuclear large and small ribosomal<br />
subunits (LSUrDNA, SSUrDNA) were used to examine the diversity, phylogenetic<br />
placement, and host affinity <strong>of</strong> forty-six endophyte species, which represented<br />
all major lineages <strong>of</strong> nonlichenized, filamentous Ascomycota. Special<br />
focus was placed on endophytes which, based on preliminary BLAST searches <strong>of</strong><br />
nrITS data, appeared to represent the Dothideomycetidae, a lineage <strong>of</strong> particular<br />
interest because it contains endophytes as well as many plant pathogens. Together,<br />
these data provide evidence for greater than expected diversity <strong>of</strong> endophytes<br />
at high-latitude sites, and provide a framework for assessing the evolution <strong>of</strong> these<br />
poorly known but ubiquitous symbionts <strong>of</strong> living plants. poster<br />
Hirooka, Yuuri*, Kobayashi, Takao and Natsuaki, Keiko, T. Lab. <strong>of</strong> Tropical<br />
Plant Protection, Tokyo University <strong>of</strong> Agriculture, 1-1-1, Sakuragaoka, Setagayaku,<br />
Tokyo 1<strong>56</strong>-8502, Japan. 70040001@nodai.ac.jp. Re-examination <strong>of</strong> Nectria<br />
sensu lato in Japan.<br />
Bionectria (Ascomycetes, Hypocreales) has white to yellow perithecia, 1septete<br />
ascospores and Clonostachys anamorph. In Japanese myc<strong>of</strong>lora, this<br />
genus includes B. bysicola, B. capitata, B. compactiuscula, B. epichloë, B. oblongispora,<br />
B. ochroleuca and B. pseudostriata. In this study, one new species <strong>of</strong><br />
Bionectria sp. h116 and its anamorph Clonostachys sp. h116 on dead twigs were<br />
collected in Okinawa and Kagoshima Pref. Surface <strong>of</strong> ascospore was warts<br />
arranged in striate. Present taxa, Bionectria species with warts arranged in striate<br />
was only B. pseudostriata Schroers (Anamorph: C. pseudostriata Schroers) from<br />
Schroers (2001). However, Bionectria sp. h116 and its anamorph differed from B.<br />
pseudostriata (Anamorph: C. pseudostriata) in the surface structure <strong>of</strong> perithecia<br />
[warted vs. smooth], color <strong>of</strong> perithecia [whitish-orange vs. orange-brown to<br />
brown], size <strong>of</strong> ascospores [15-21 X 5-7.5 µm vs. 9-17 X 3-6 µm], and size <strong>of</strong><br />
conidia [3-16 X 2-4 µm vs. 3.6-8 X 2-3.8 µm]. This species belongs to the subgenus<br />
Bionectria (Schroers 2001). Two other species <strong>of</strong> this genus also have been<br />
collected from Japan for the first time; B. grammicospora Schroers & Samuels<br />
(Anamorph: C. grammicospora Schroers & Samuels) in Miyagi Pref. and B.<br />
sporodochialis Schroers (Anamorph: C. sporodochialis Schroers) in various parts<br />
<strong>of</strong> Japan. poster<br />
Hirose, Dai. Graduate school <strong>of</strong> life and environmental science, University <strong>of</strong><br />
Tsukuba, Sugadaira Montane Research Center, Sugadaira, Nagano 386-2201,<br />
Japan. daihiro@sugadaira.tsukuba.ac.jp. Ecology <strong>of</strong> ectomycorrhizal fungi:<br />
population structure and biogeography.<br />
Population structures <strong>of</strong> ectomycorrhizal (ECM) fungi in various ecosystems<br />
have been studied extensively using molecular ecological methods. These<br />
studies have showed the propagation manners <strong>of</strong> various ECM fungi in natural<br />
ecosystems. It is important to select a proper fungal species in studying the population<br />
<strong>of</strong> ECM fungi, since a host tree is always associated with diverse ECM<br />
fungi. We have studied the ecology <strong>of</strong> Suillus pictus which colonizes and forms<br />
ectomycorrhizas on fine roots <strong>of</strong> Japanese five-needled pine species. This fungus<br />
is suitable for the study <strong>of</strong> population ecology <strong>of</strong> ECM fungi. The reasons are as<br />
follows. (1) It is a dominant ECM fungus colonizing on fine roots <strong>of</strong> the pine<br />
species, (2) forms macroscopic tubercle mycorrhizas which can be easily identified<br />
and isolated, and (3) has a narrow host range in nature like as other Suillus<br />
spp. that have been widely studied from ecological and ecophysiological view<br />
points. In addition, the host pines are distributed in relatively high altitude places<br />
in isolation in Japan. We studied following subjects on this fungus: (1) its host<br />
range in experimental conditions, (2) distribution pattern in a plantation stand, (3)<br />
population structures in natural forest stands, and (4) comparison <strong>of</strong> local populations<br />
in Japan. Based on the results <strong>of</strong> these studies, we discuss ecological characteristics<br />
<strong>of</strong> S. pictus, and its biogeography. symposium presentation<br />
Hirotoshi, Sato 1 *, Takakazu, Yumoto 2 and Noriaki, Murakami 1 . 1 Lab <strong>of</strong> Plant<br />
Taxonomy and Evolution, Department <strong>of</strong> Botany, Graduate School <strong>of</strong> Science,<br />
Kyoto University, Oiwake-cho, Kitashirakawa, Sakyo-ku, Kyoto-shi, Kyoto,<br />
606-8502 Japan, 2 Research Institute <strong>of</strong> Humanity and Nature, National Institutes<br />
for the Humanities, Inter-University Research Institute Corporation, 335<br />
Takashima-cho, Marutamachi-dori Kawaramachi nishi-iru, Kyoto 602-0878,<br />
Japan. kuritake@fj8.so-net.ne.jp. Cryptic species and host specificity in the ec-<br />
Continued on following page<br />
<strong>Inoculum</strong> <strong>56</strong>(4), November 2005 25