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Book of Abstracts (PDF) - International Mycological Association

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IMC7 Main Congress Theme IV: POPULATION DYNAMICS AND ECOLOGY Posters<br />

fresh ruminal digesta = 5.31. MPN values obtained from<br />

fresh faeces, frozen faeces and fresh ruminal digesta were<br />

similar (P > 0.05). The mean values from faecal and<br />

ruminal samples <strong>of</strong> 3 cattle for different substrates were as<br />

follow; glucose = 5.11; cellobiose = 5.23; xylan = 4.75;<br />

wheat straw = 5.53 and cellulose = 5.11. Wheat straw gave<br />

significantly (P < 0.05) higher viable counts than glucose,<br />

xylan and cellulose. Population densities, obtained when<br />

glucose, cellulose and xylan used, were similar (P> 0.05).<br />

1020 - Ectomycorrhizal fungal dynamics <strong>of</strong> one- and<br />

two-year-old Norway spruce seedlings after planting to<br />

mounded forest clear-cut<br />

T. Pennanen 1* & J. Heiskanen 2<br />

1 Finnish Forest Research Institute, Vantaa Research<br />

Centre, P.O.B. 18, 01301 Vantaa, Finland. - 2 Suonenjoki<br />

Research Station, 77600 Suonenjoki, Finland. - E-mail:<br />

taina.pennanen@metla.fi<br />

Container Norway spruce seedlings were planted on two<br />

clearcut and mounded Myrtillus type sites in Central<br />

Finland. Seedlings were planted on mounds and on<br />

untreated spots between mounds. Seedlings were sampled<br />

before and one and two growing seasons after planting for<br />

detailed measurement <strong>of</strong> root and shoot attributes and for<br />

morphological and molecular characterization <strong>of</strong><br />

ectomycorrhiza (ECM) in roots grown out into the soil.<br />

Different morphological groups were subsampled for PCR-<br />

DGGE analysis <strong>of</strong> 18S rRNA gene region in order to<br />

separate ECM in detail. During the first growing season,<br />

one-year old seedlings grew better in shoot height than the<br />

two-year-old. However, root egress from containers into<br />

the surrounding soil was greater in the two-year-old<br />

seedlings during both first and second summer after<br />

planting. The outgrown root length and the number <strong>of</strong> root<br />

tips per length were greater on mounds than on untreated<br />

spots. Totally 17 different morphotypes were observed and<br />

6 <strong>of</strong> them were present in all treatments. Neither age <strong>of</strong> the<br />

seedling nor duration in the field did affect the richness <strong>of</strong><br />

ECM morphotypes but there was a clear temporal shift in<br />

the proportions <strong>of</strong> 3 major morphotypes. The smooth white<br />

type was the most dominant morphotype before outplanting<br />

but almost disappeared in two years in the field. In<br />

contrast, the proportion <strong>of</strong> the smooth brown type increased<br />

up to 58-78% after two years. The smooth dark brown type<br />

increased especially on mounds.<br />

1021 - Pleurotus spp. characterization by microsatellitebased<br />

DNA fingerprinting<br />

P. Rapanà 1* , A. Rubini 2 & F. Di Mario 1<br />

1 CNR IBAF - IBESM, Area della Ricerca di Roma, Via<br />

Salaria km 29.300; 00016 Monterotondo Sc. (Roma), Italy.<br />

- 2 CNR IRMGPF, Via della Madonna Alta n.130, 06128<br />

Perugia, Italy. - E-mail: pompilio.rapana@mlib.cnr.it<br />

308<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong><br />

Characterizing fungal species and varieties through<br />

microsatellite is a powerful approach to evaluate<br />

biodiversity and genetic relationships among populations.<br />

Four ISSR (inter simple sequence repeats) primers have<br />

been utilized to characterize fungal species and varieties<br />

among Pleurotus genus. Five strains <strong>of</strong> each<br />

species/varieties (P. ostreatus, P. eryngii, P. eryngii var.<br />

ferulae, P. eryngii var. nebrodensis) have been analyzed<br />

and ISSR data were subject to cluster analysis performed<br />

with UPGMA method using Dice and Jaccard coefficients.<br />

This analysis clearly showed two distinctive cluster, one<br />

related to P. ostreatus and one to P. eryngii var. ferulae,<br />

whereas less clear relationships appeared between P.<br />

eryngii and P. eryngii var. nebrodensis. Further<br />

investigation are in progress to analyze additional<br />

Pleurotus strains and to test different ISSR primers as well<br />

as to identify microsatellite-containing amplicons.<br />

1022 - The polymorphic nature <strong>of</strong> the rRNA LSU gene<br />

<strong>of</strong> arbuscular mycorrhizal fungi (AMF) spores<br />

A. Rodriguez 1* , J.C. Dodd 2 & J.P. Clapp 3<br />

1 University <strong>of</strong> Hohenheim, Universität Hohenheim (340),<br />

D-70593 Stuttgart, Germany. - 2 Sittingbourne Enterprise<br />

Hub, Sittingbourne Research Centre, Sittingbourne, Kent<br />

ME9 8AG, U.K. - 3 University <strong>of</strong> Kent at Canterbury,<br />

Canterbury, Kent CT2 7NJ, U.K. - E-mail: aliarodr@unihohenheim.de<br />

Sequencing <strong>of</strong> ribosomal RNA genes has been extensively<br />

exploited in attempts to identify and determine<br />

phylogenetic relationships and genetic heterogeneity <strong>of</strong><br />

AMF. The heterogeneity <strong>of</strong> rRNA genes within single<br />

spores and isolates <strong>of</strong> AMF has been recognised for several<br />

years, however the magnitude <strong>of</strong> this variation has been<br />

ignored in most taxonomic and phylogenetic analyses.<br />

Sequence diversity has crucial implications for the<br />

interpretation <strong>of</strong> AMF biodiversity and the species concept<br />

in these fungi. We report here the first investigation <strong>of</strong><br />

genetic diversity in AMF where variation has been<br />

assessed using sample sizes <strong>of</strong> several hundred sequences.<br />

The study concentrated on a well characterised species <strong>of</strong><br />

AMF, Glomus coronatum, but also included three other<br />

Glomus species with similar spore morphologies. In total<br />

435 clones containing the LSU D2 regions from 7 isolates<br />

<strong>of</strong> G. coronatum (80% <strong>of</strong> isolates currently available) as<br />

well as isolates <strong>of</strong> Glomus mosseae, Glomus geosporum<br />

and Glomus constrictum, were screened for sequence<br />

variation using a PCR-single strand conformational<br />

polymorphism (PCR-SSCP) technique. The variation<br />

encountered was higher than expected, 138 representative<br />

sequences were obtained and analysis indicated that most<br />

were unique. This variation could not be attributed to DNA<br />

polymerase or cloning artefacts. Implications for the<br />

species concept in AMF, the use <strong>of</strong> rRNA sequences to<br />

estimate biodiversity and in situ detection in field ecology<br />

are discussed.

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