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 II: SYSTEMATICS, PHYLOGENY AND EVOLUTION Posters<br />
650 - The mating relationships <strong>of</strong> the S and F groups <strong>of</strong><br />
Heterobasidion annosum in Northern Hemisphere<br />
Y.C. Dai 1* , T. Niemelä 2 & K. Korhonen 3<br />
1 Institute <strong>of</strong> Applied Ecology, Academia Sinica, Shenyang<br />
110016, Wenhua Road 72, China. - 2 Botanical Museum,<br />
University <strong>of</strong> Helsinki, P.O. Box 47, FIN-00017, Finland. -<br />
3 Finnish Forest Research Institute, P.O. Box 18, FIN-<br />
01301 Vantaa, Finland. - E-mail: yuchengd@yahoo.com<br />
Pairings made among homokaryons <strong>of</strong> Heterobasidion<br />
parviporum Niemelä & Korhonen (S group <strong>of</strong> the H.<br />
annosum complex) from Europe, Northeast China and<br />
Northwest North America, and the European H. abietinum<br />
Niemelä & Korhonen (F group) showed that the Northeast<br />
Chinese S has the strongest mating capacity among all the<br />
testers, being closely related with the European S and F,<br />
and also the North American S. The North American S is<br />
more readily compatible with the European F than with the<br />
European S, and it seems that the so-called North<br />
American S group should be referred to the European F<br />
group rather than the European S. Samples collected from<br />
North Yunnan (eastern foothills <strong>of</strong> the Himalayas, China)<br />
were paired with testers <strong>of</strong> the S group from NE China,<br />
with P, S and F groups from Europe, and S group from NW<br />
North America; the Yunnan stocks mated with all the<br />
testers by frequency over 90%. This suggests that the<br />
Yunnanese stocks have the largest effective population<br />
size.<br />
651 - Systematics and evolution <strong>of</strong> Gomphales<br />
(Basidiomycetes)<br />
P.P. Daniëls * , M.P. Martín & M.T. Tellería<br />
Real Jardín Botánico, C.S.I.C., Plaza de Murillo, 2, 28014<br />
Madrid, Spain. - E-mail: daniels@ma-rjb.csic.es<br />
The order Gomphales enclose eight genera in the world and<br />
Ramaria is the main one in relation to species number.<br />
Previous systematic arrangement in subgenus Ramaria was<br />
proposed by Frachi & Marchetti (2001, Fungi non<br />
delineati. 16). This subgenus was divided into ten sections<br />
only based upon the presence/absence <strong>of</strong> clamped hyphae<br />
and the basidiome colour. As part <strong>of</strong> a monograph <strong>of</strong> the<br />
Iberian Gomphales a phylogenetic study in Gomphales<br />
focused on Ramaria has been undertaken. Thirty-four<br />
species <strong>of</strong> Ramaria as well as other genera <strong>of</strong> Gomphales<br />
were included in the phylogenetic analysis based on ITS<br />
and 5.8S rDNA sequences. Moreover, phylogenetic<br />
analysis <strong>of</strong> the morphological characters were done on<br />
clavarioid basidiomes. The very variable ITS regions gave<br />
low bootstrap values but it can be deduced some<br />
considerations about the systematics and evolution <strong>of</strong> the<br />
Gomphales: 1) Subgenus Echinoramaria is monophyletic.<br />
2) Ramaria is a genus related with several taxa among the<br />
Gomphales, Gautieria morchellaeformis is related with<br />
Section Ramariae and Gomphus clavatus with Section<br />
Fennicae. 3) Ramaria bataillei and R. pumila seems to be a<br />
bridge between the ectomycorrhizal and the saprobic<br />
Ramarias. 4) Lentaria and Hydnocristella are closely<br />
related with subgenus Lentoramaria. 5) The gelatinose<br />
texture <strong>of</strong> the fruitbodies seems to be a synapomorphy. 6)<br />
Clamp connections and fruitbody colour are very<br />
homoplasic characters and do not serve to divide sections<br />
among Ramaria.<br />
652 - Another canker-causing aerial Phytophthora from<br />
forest trees in California and Oregon<br />
J.M. Davidson 1 , M.M. Garbelotto 2 , E.M. Hansen 3* , P.<br />
Reeser 3 & D.M. Rizzo 1<br />
1 Plant Pathology, University <strong>of</strong> California, Davis CA<br />
95616, U.S.A. - 2 Environmental Science Policy and<br />
Management, U. C. Berkeley, Berkeley CA 94720, U.S.A. -<br />
3 Botany and Plant Pathology, Oregon State University,<br />
Corvallis OR 97331, U.S.A. - E-mail:<br />
hansene@bcc.orst.edu<br />
Two distinct Phytophthora species cause similar symptoms<br />
on several western forest trees. P. ramorum causes lethal<br />
cankers (sudden oak death) on tanoak and coast live oak<br />
trees and foliar and dieback symptoms on other tree and<br />
shrub species in some western forests. A second<br />
Phytophthora species, previously undescribed, is<br />
occasionally isolated from lethal cankers on tanoak and<br />
coast live oak, and from foliar lesions on Umbellularia and<br />
other hosts, in areas where P. ramorum is also active. ITS<br />
DNA sequence indicates close relationship to P. ilicis (a<br />
foliar pathogen <strong>of</strong> holly) and P. psychrophila (newly<br />
described from European oak forest soils). It is homothallic<br />
with amphigynous antheridia, and has deciduous sporangia.<br />
It grows more slowly, with a lower temperature optimum,<br />
than P. ramorum. In log inoculation tests it is nearly as<br />
pathogenic to tanoak as P. ramorum. It does not infect<br />
holly leaves in leaf inoculation tests. In the forest it is<br />
usually associated with single killed trees, in contrast to the<br />
expanding patches <strong>of</strong> mortality caused by P. ramorum.<br />
653 - Endophytes from leafy liverworts: a molecular<br />
phylogenetic perspective<br />
C. Davis<br />
Duke University, Biological Sciences, Box 90338, Durham,<br />
NC, U.S.A. - E-mail: ecf5@duke.edu<br />
It has long been known that leafy liverworts possess<br />
endophytic fungi, but these fungi have not previously been<br />
identified with precision. Here, I present results <strong>of</strong><br />
molecular phylogeny as the means to identify these<br />
endosymbionts from selected leafy liverworts. I address<br />
possible explanations for the nature <strong>of</strong> such symbioses. I<br />
discuss hypotheses regarding liverwort structural<br />
adaptations for endosymbiosis, and explore methodology to<br />
test these hypotheses.<br />
<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong> 197