Book of Abstracts (PDF) - International Mycological Association
Book of Abstracts (PDF) - International Mycological Association
Book of Abstracts (PDF) - International Mycological Association
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IMC7 Main Congress Theme IV: POPULATION DYNAMICS AND ECOLOGY Posters<br />
We compared interspecific interactions in fresh beech<br />
wood and beech wood partly decayed by the primary decay<br />
agents, Eutypa spinosa, Fomes fomentarius, Stereum<br />
hirsutum and Trametes versicolor. The fungi used in the<br />
experiments included five secondary decay agents,<br />
common on beech wood in advanced decay, as well as the<br />
aforementioned primary decayers. The experiments were<br />
carried out using sterilised, recolonised wood and lasted for<br />
seven months. Interactions involving secondary decayers<br />
were affected by wood type, with outcomes changing from<br />
complete replacement to deadlock in at least three species<br />
combinations. Most <strong>of</strong> the secondary decayers were able to<br />
replace some <strong>of</strong> the primary decayers. However, several <strong>of</strong><br />
the secondary decayers were unable to colonise sterilised<br />
wood decayed by Trametes versicolor or Stereum<br />
hirstutum. This lead to a new series <strong>of</strong> experiments in<br />
which the effects <strong>of</strong> exudates from fresh and partly decayed<br />
wood were investigated with respect to hyphal extension<br />
rates in a larger range <strong>of</strong> secondary decay fungi. Sterilised<br />
wood pieces were placed on 0,5% malt agar, opposite to<br />
small plugs containing the test fungi, which showed very<br />
variable growth responses to the various wood types. Most<br />
species increased hyphal extension rates as response to<br />
wood decayed by Eutypa spinosa and Fomes fomentarius,<br />
while wood decayed by Stereum hirsutum resulted in<br />
reduced or completely lacking growth in a majority <strong>of</strong><br />
species.<br />
972 - Physiological characteristics <strong>of</strong> symbiotic fungi<br />
associated with the seed germination <strong>of</strong> Gastrodia elata<br />
I.P. Hong 1* , S.X. Guo 2 , T.S. Lee 3 & M.W. Lee 4<br />
1 Division <strong>of</strong> Seri-Culture and Api-culture, NIAST, Suwon,<br />
441-707, Korea. - 2 Institute <strong>of</strong> Medicinal Plant, Chinese<br />
Academy <strong>of</strong> Medical Sciences, P. R., China. - 3 Department<br />
<strong>of</strong> Biology, Incheon University, 177, Dohwa-dong, Nam-<br />
Ku, 402-749, Korea. - 4 Department <strong>of</strong> Biology, Dongguk<br />
University, 26, Pil-Dong 3ga, Chunggu, Seoul, 100-715,<br />
Korea.<br />
This study was carried out to investigate the possibility for<br />
seeds germination <strong>of</strong> Gastrodia elata using symbiotic<br />
fungi. Since seeds <strong>of</strong> G. elata are very small and lack an<br />
endosperm and other nutrients, their germination is<br />
difficult without requirement for external nutrients. Out <strong>of</strong><br />
twenty six isolates collected from protocorms <strong>of</strong> G. elata<br />
and roots <strong>of</strong> native orchids inhabited in wild, two strains<br />
(H-2 and H-21) were observed to stimulate the seed<br />
germination <strong>of</strong> G. elata. The seed germination <strong>of</strong> G. elata<br />
was excellent on oak tree leaves medium. The optimal<br />
conditions for mycelial growth <strong>of</strong> symbiotic fungi were 25<br />
°C and pH 6.0, respectively. The mycelial growth <strong>of</strong> H-2<br />
strain was excellent on YMA medium, while h-21 was<br />
poor on PDA medium. In case <strong>of</strong> carbon sources, the<br />
mycelial growth <strong>of</strong> H-2 and H-21 was good on media<br />
supplemented with glucose and dextrin, respectively.<br />
Calcium nitrate was good for mycelial growth <strong>of</strong> H-2 strain<br />
as a nitrogen sources, whereas urea was effective to H-21<br />
strain.<br />
973 - Classification <strong>of</strong> wood decay fungi isolated from<br />
durable wood species, ekki<br />
S. Horisawa 1* , R. Ito 2 , Y. Sakuma 3 & S. Doi 1<br />
1 Institution <strong>of</strong> Wood Technology, Akita Prefectural<br />
University, 11-1 Kaieizaka, Noshiro, Akita 016-0876,<br />
Japan. - 2 Akita Wood Technology Transfer Foundation, 11-<br />
1 Kaieizaka, Noshiro, Akita 016-0876, Japan. - 3 Biological<br />
Resources Division, Japan <strong>International</strong> Research Center<br />
for Agricultural Sciences (JIRCAS), 1-1 Ohwashi, Tsukuba,<br />
Ibaraki 305-0074, Japan. - E-mail: horisawa@iwt.akitapu.ac.jp<br />
Ekki (Azobe, Bongossi; Lophira alata Banks), a native<br />
African wood species, is known as a large durable species<br />
and has been utilized without preservative treatment for<br />
outdoor architectures such as bridges in EU. In Japan,<br />
however, several bridges <strong>of</strong> ekki wood are decayed in a<br />
short time after construction. In this study, as the first step<br />
<strong>of</strong> the elucidation <strong>of</strong> decay in ekki wood, basidiomycetes<br />
isolated from damaged members <strong>of</strong> ekki bridges were<br />
classified by PCR-RFLP. Decayed wood pieces and fruit<br />
bodies from ekki bridges were incubated on potatodextrose-agar<br />
plates containing antibiotics. Twenty-six<br />
isolates <strong>of</strong> basidiomycetes were obtained from different<br />
areas in Japan. One <strong>of</strong> the isolates was identified<br />
morphologically as Perenniporia tephropora (Mont.) Ryv.<br />
(Loweporus tephroporus). Genomic DNAs were extracted<br />
from isolates using the benzyl chloride method. The whole<br />
inter specific transcribed (ITS) regions (ITS1, ITS2, and<br />
5.8S) were amplified by PCR. The PCR products were<br />
digested with 4 restriction enzymes to obtain RFLPs.<br />
Restricted fragments were separated by electrophoresis in<br />
8% <strong>of</strong> polyacrylamide gel. Comparing fragment patterns,<br />
14 isolates were identified as P. tephropora. To obtain<br />
further molecular information on the decay basidiomycetes,<br />
we undertake to determine sequences <strong>of</strong> 18S rDNAs.<br />
974 - Aspergillus section Flavi in the United States:<br />
characterization <strong>of</strong> soil populations from agricultural<br />
fields<br />
B.W. Horn<br />
National Peanut Research Laboratory, United States<br />
Department <strong>of</strong> Agriculture, Agricultural Research Service,<br />
P.O. Box 509, Dawson, Georgia 31742-0509, U.S.A.<br />
Species belonging to Aspergillus section Flavi <strong>of</strong>ten<br />
produce aflatoxins and cyclopiazonic acid, mycotoxins that<br />
contaminate preharvest peanuts, corn and cottonseed. Soil<br />
populations <strong>of</strong> A. flavus, A. parasiticus, A. nomius, A.<br />
tamarii and A. caelatus were examined over a large<br />
geographic area within the United States and in greater<br />
detail within a single field. A transect was established from<br />
New Mexico to Virginia, and species from section Flavi<br />
showed distinct patterns in their geographic distribution. A.<br />
flavus (large sclerotial morphotype or L strain) was the<br />
most widely distributed species, but A. flavus var.<br />
<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong> 293