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Book of Abstracts (PDF) - International Mycological Association

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IMC7 Main Congress Theme II: SYSTEMATICS, PHYLOGENY AND EVOLUTION Posters<br />

745 - Characterization <strong>of</strong> Laetiporus sulphureus<br />

complex in Japan using phylogenetic analyses,<br />

morphological study and incompatibility tests<br />

Y. Ota * & T. Hattori<br />

Forestry and Forest Products Research Institute, Tsukuba,<br />

305-8687, Japan. - E-mail: yuota@ffpri.affrc.go.jp<br />

Phylogenetic analyses, morphological studies and<br />

incompatibility tests were conducted to define intra-generic<br />

taxa <strong>of</strong> Japanese Laetiporus sulphureus complex.<br />

Phylogenetic analyses based on the nucleotide sequences <strong>of</strong><br />

the ITS regions <strong>of</strong> the ribosomal DNA and beta-tubulin<br />

gene suggest that Japanese Laetiporus spp. are divided into<br />

four distinct groups (groups A-D). European population <strong>of</strong><br />

L. sulphureus is clearly distinct from all Japanese groups.<br />

Each group shares similar morphological characteristics<br />

and host range (conifers vs. hardwoods). Group A has a<br />

white pore layer, pinkish orange pileus surface, and<br />

imbricated pilei. This group is distributed in the cooltemperate<br />

area and associated with hardwoods. Group B<br />

has lemon yellow pore layer, pinkish orange pileus surface,<br />

and imbricated pilei. This group is associated with conifers.<br />

Group C has a lemon yellow pore layer, yellow pileus<br />

surface and non-imbricated pilei. Sometimes it produces<br />

semi-globose basidiocarps with abundant chlamydospores<br />

in the context. Group C is distributed in the warmtemperate<br />

area <strong>of</strong> central parts <strong>of</strong> Japan. Group D has a<br />

lemon yellow pore layer and pinkish orange to yellow<br />

pileus surface. This group also produces semi-globose<br />

form. This group is distributed in the warm-temperate to<br />

subtropical areas <strong>of</strong> southern part <strong>of</strong> Japan. Single spore<br />

isolates from groups A, B and C were incompatible each<br />

other, which revealed that L. sulphureus complex in Japan<br />

is composed <strong>of</strong> at least three species.<br />

746 - Penicillium tulipae and P. carotae, two new species<br />

belonging to the series Corymbifera<br />

D.P. Overy * & J.C. Frisvad<br />

Mycology Group, Bio-Centrum, DTU, Building 221,<br />

Danish Technical University, DK-2800, Kgs. Lyngby,<br />

Denmark. - E-mail: do@biocentrum.dtu.dk<br />

Taxa <strong>of</strong> the Penicillium series Corymbifera are known for<br />

their synnemata and association with the rhizosphere <strong>of</strong><br />

vegetables, most commonly with bulbs. The known species<br />

P. allii, causing a storage rot <strong>of</strong> garlic, P. hordei, associated<br />

with cereals, and P. hirsutum associated with a variety <strong>of</strong><br />

vegetables can easily be separated based on colony<br />

morphology. The concepts <strong>of</strong> P. albocoremium and P.<br />

venetum, reported to cause a severe bulb rot on a variety <strong>of</strong><br />

commercially grown flower and Allium species, later<br />

evolved from P. hirustum senso lato as a response to<br />

apparent differences in secondary metabolism. Further<br />

secondary metabolite investigations involving P.<br />

albocoremium indicated the potential presence <strong>of</strong> two or<br />

more taxa. Described here using micromorphology, colony<br />

characteristics on various media and chemotaxonomic<br />

pr<strong>of</strong>iling are P. albocoremium sensu stricto and two new<br />

species, P. tulipae and P. carotae, which were resolved<br />

during a taxonomic survey <strong>of</strong> P. albocoremium isolates<br />

contained within the IBT culture collection. Although these<br />

novel taxa are micromorphologically quite similar, their<br />

unique secondary metabolite pr<strong>of</strong>iles individually<br />

distinguish them from isolates <strong>of</strong> P. albocoremium.<br />

Moreover, these bulb associated species produce the<br />

following mycotoxins: citrinin, penicillic acid and terrestric<br />

acid by P. carotae and penitrem A and terrestric acid by P.<br />

tulipae.<br />

747 - Cladistic biogeography <strong>of</strong> Lignincola laevis<br />

(Halosphaeriales, Ascomycota)<br />

K.L. Pang 1* , E.B.G. Jones 2 , L.L.P. Vrijmoed 3 & R.Y.C.<br />

Kong 3<br />

1 School <strong>of</strong> Biological Sciences, University <strong>of</strong> Portsmouth,<br />

King Henry Building, King Henry I Street, Portsmouth<br />

PO1 2DY, England, U.K. - 2 BIOTEC, National Centre for<br />

Genetic Engineering and Biotechnology, 113, Thailand<br />

Science Park, Paholyothin Road, Klong 1, Klong Luang,<br />

Pathumthani, 12120, Thailand. - 3 Department <strong>of</strong> Biology<br />

and Chemistry, City University <strong>of</strong> Hong Kong, 83 Tat Chee<br />

Avenue, Kowloon Tong, Hong Kong, China. - E-mail: kalai.pang@port.ac.uk<br />

Partial large subunit and the ITS regions <strong>of</strong> the ribosomal<br />

DNA <strong>of</strong> ten Lignincola laevis strains, which were isolated<br />

from different geographical locations, substrata and habitat,<br />

were sequenced and subjected to phylogenetic analysis to<br />

determine their genetic difference. These strains do not<br />

form distinct geographical groupings. No correlation was<br />

discovered between strains and habitat as freshwater and<br />

marine water isolates <strong>of</strong> L. laevis form a coherent and wellsupported<br />

group. Strains isolated from mangroves form a<br />

robust clade while isolates from other substrata constitute<br />

others. Different genes infer different phylogeny for two L.<br />

laevis strains. These results suggest that ascospores (asci)<br />

<strong>of</strong> L. laevis may be able to disperse over long distances.<br />

More strains from wider geographical locations, different<br />

habitats (freshwater, brackish water and marine water) and<br />

different substrata should be explored to explain the current<br />

distribution pattern and evolution <strong>of</strong> aquatic fungi.<br />

748 - Phylogenetic relationships <strong>of</strong> Hydnodon Banker<br />

V. Patiño-Conde 1* , D. González 2 , J. Cifuentes 1 , M.<br />

Villegas 1 & R. García-Sandoval 1<br />

1 FCME Herbario, UNAM., PO Box 70-399, Cd.<br />

Universitaria, CP 04510, DF., Mexico. - 2 Sistemática<br />

Vegetal, Instituto de Ecología AC, PO Box 63, Xalapa, CP<br />

91000, Veracruz, Mexico. - E-mail:<br />

viole_pconde@correo.unam.mx<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong> 225

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