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Inoculum 56(4) - Mycological Society of America

Inoculum 56(4) - Mycological Society of America

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MSA ABSTRACTS<br />

Degawa, Yousuke. Kanagawa Prefectural Museum <strong>of</strong> Natural History, 499,<br />

Iryuda, Odawara, Kanagawa 250-0031, Japan. degawa@nh.kanagawa-museum.jp.<br />

Taxonomic studies on the family Mortierellaceae.<br />

The family Mortierellaceae is one <strong>of</strong> the well-known soil fungi, including<br />

about 100 spp. The difficulties to maintain their sporulation and insufficient information<br />

on sexual reproduction prevented constructing a natural classification<br />

<strong>of</strong> the family. Direct field observation on their microhabitats enabled to establish<br />

a baiting method for selective isolation <strong>of</strong> each species, and a good condition for<br />

inducing the sexual reproduction. Using the dead bodies <strong>of</strong> arthropods as baits,<br />

new or rare species were repeatedly obtained. Six species <strong>of</strong> them belonged to the<br />

Section Actinomortierella, four <strong>of</strong> which were new. Five <strong>of</strong> them were heterothallic<br />

and showed new style <strong>of</strong> zygospore formation on the medium containing<br />

arthropods. Based on these ecological and morphological characters, the concept<br />

<strong>of</strong> the section was revised, and treated it as an independent genus. Five<br />

heterothallic species <strong>of</strong> the genus Actinomortirella were biologically isolated. Furthermore,<br />

within A. capitata, morphologically identical two intraspecific isolated<br />

mating groups were detected. They showed clear differences in geographical distribution<br />

(tropical and temperate area), and temperature ranges for mycelial<br />

growth and zygospore production. Molecular analysis on 18SrDNA ITS region<br />

suggested that each mating group should be treated as an independent species respectively.<br />

contributed presentation: MSJ Research Encouragement Award<br />

Lecture<br />

Degawa, Yousuke 1 * and Sato, Hiroki 2 . 1 Kanagawa Prefectural Museum <strong>of</strong> Natural<br />

History, 499, Iryuda, Odawara, Kanagawa 250-0031, Japan, 2 Kyushu Research<br />

Center, Forestry and Forest Research Institute, 11-16, Kurokami 4 chome,<br />

Kumamoto, Kumamoto 860-0862, Japan. degawa@nh.kanagawa-museum.jp.<br />

How to clarify the true status <strong>of</strong> anamorphic Trichomycetes? -an approach<br />

based on the observation <strong>of</strong> its host animal behavior.<br />

The orders Asellariales and Eccrinales are anamorphic Trichomycetes, in<br />

which neither zygospore nor trichospore has been known. Do they lose these<br />

kinds <strong>of</strong> spores? Careful observations on the living hosts brought us invaluable<br />

hints for solving this question. In Orchesellaria mauguioi (Asellariales), trichospore-like<br />

spore formation was observed when the hosts (Isotomurus sp.) were<br />

keeping on the water in chamber. They <strong>of</strong>ten molted and their shed molts floated<br />

on the water. The fungal thalli were situated at the lower surface <strong>of</strong> the molts in<br />

water. Arthrospores germinated to produce short stalks penetrating the molt and<br />

bearing the thick walled, cylindrical spores on their tips. Each spore accompanied<br />

a bowling-pin-shaped thin walled cell with external long appendage, which reminds<br />

us the fructification <strong>of</strong> the genus Orphella. When the millipede (Epanerchodus<br />

sp.), a host <strong>of</strong> Enterobryus sp. (Eccrinales) was keeping in moist chamber,<br />

peculiar conidiophore with mushroom-shaped conidia <strong>of</strong>ten emerged on the accumulated<br />

dungs <strong>of</strong> hosts. This fungus was identified as a rare hyphomycete,<br />

Aenigmatospora pulchra R. F. Castaneda Ruiz et al., described from Cuba. The<br />

stalk <strong>of</strong> this fungus was constantly connected to the short cylindrical 2 or 3-celled<br />

hyphal segments, similar to the arthrospores <strong>of</strong> Enterobryus sp., buried in the<br />

dung. The implications <strong>of</strong> these newly found spores are discussed. symposium<br />

presentation<br />

Dentinger, Bryn C.* and McLaughlin, David J. Plant Biological Sciences, University<br />

<strong>of</strong> Minnesota, St. Paul, MN 55108, USA. dent0015@umn.edu. Homoplastic<br />

surgery: reconstructing the classification <strong>of</strong> two coral mushroom<br />

families (Clavariaceae and Pterulaceae).<br />

Club and coral fungi are a polyphyletic assemblage <strong>of</strong> hymenomycetous<br />

mushrooms. The clavarioid sporocarp has repeatedly evolved in the Homobasidiomycetidae<br />

(Pine et al. 1999), yet to what degree this morphology is homoplasious<br />

is still not completely known. We evaluated the systematics <strong>of</strong> the coral<br />

mushroom families Clavariaceae and Pterulaceae using DNA sequence data and<br />

multiple phylogenetic methods. We generated 35 sequences from the 5’ region <strong>of</strong><br />

the nucLSU rDNA spanning 10 genera and 19 species <strong>of</strong> clavarioid fungi. These<br />

sequences, plus 45 published sequences, were aligned to the dataset <strong>of</strong> Moncalvo<br />

et al. (2002) and analyzed under the parsimony criterion. Based on this analysis,<br />

subsets <strong>of</strong> Clavaria and Pterulaceae were evaluated separately to obtain better resolution<br />

within each group. Our preliminary results indicate that both Clavariaceae<br />

and Pterulaceae need to be revised in order to reflect a monophyletic classification.<br />

The genus Clavaria appears to be monophyletic, but also requires revision<br />

to include some species while excluding others. Several species <strong>of</strong> Pterula are<br />

identified within the G2 cultivar clade <strong>of</strong> fungus-farming ants for the first time.<br />

These results provide a preliminary view <strong>of</strong> the systematics <strong>of</strong> two core families<br />

<strong>of</strong> coral mushrooms, contribute to understanding the history <strong>of</strong> the ant-fungus mutualism,<br />

and present a framework for future investigation. poster<br />

Desjardin, Dennis E. 1 * and Hemmes, Don E. 2 1 Dept. <strong>of</strong> Biology, San Francisco<br />

State University, San Francisco, CA 94132, USA, 2 Dept. <strong>of</strong> Biology, University<br />

<strong>of</strong> Hawai`i, Hilo, Hawai`i 96720, USA. ded@sfsu.edu. Agaricales <strong>of</strong> the native<br />

forests <strong>of</strong> Hawai`i.<br />

The Hawaiian Archipelago is the most isolated oceanic island group on<br />

earth. Constantly forming, migrating and subsiding, the volcanic chain has formed<br />

land that has remained above sea level continuously for the past 29 million years,<br />

resulting in terrestrial laboratories for the evolution <strong>of</strong> a diverse biota. Human<br />

16 <strong>Inoculum</strong> <strong>56</strong>(4), August 2005<br />

habitation over the past 2000 years has dramatically impacted the landscape. Currently,<br />

over 90 % <strong>of</strong> Hawaiian terrestrial habitats are dominated by introduced<br />

plants (>4600 spp.), whereas less than 10 % remains in undisturbed native forests.<br />

As a consequence <strong>of</strong> these factors, the Islands display some <strong>of</strong> the highest levels<br />

<strong>of</strong> endemism and extinction documented to date. The diversity <strong>of</strong> Hawaiian Agaricales<br />

also reflects these factors. Of the 335 species documented by us to date, 275<br />

are associated with introduced plants in non-native habitats, whereas only 60<br />

species (18 %) are known from native habitats and are considered by us as native<br />

species with 75 % endemism. Surprising observations include: the low diversity<br />

<strong>of</strong> native Agaricales; no native Hawaiian trees support ectomycorrhizae; native<br />

Hawaiian Agaricales are dominated by Tricholomataceae s.l. and Hygrophoraceae<br />

s.l.; there is very limited adaptive radiation within native agaric lineages.<br />

We will present data from 12 years <strong>of</strong> fieldwork, focused on the diversity<br />

and origins <strong>of</strong> native Hawaiian Agaricales. symposium presentation<br />

Dickie, Ian A. 1 *, Dentinger, Bryn C. 4 , Avis, Pete G. 3 , McLaughlin, David J. 4 and<br />

Reich, P. B. 2 1 Landcare Research - Manaaki Whenua, P.O. Box 69, Lincoln, Canterbury,<br />

New Zealand, 2 Department <strong>of</strong> Forest Resources, University <strong>of</strong> Minnesota,<br />

Green Hall, 1530 Cleveland Ave. N., St. Paul, MN 55108, USA, 3 Chicago<br />

Field Museum <strong>of</strong> Natural History, Botany Department, Roosevelt Rd. at<br />

Lakeshore Drive, Chicago, IL 60605, USA, 4 Department <strong>of</strong> Plant Biology, University<br />

<strong>of</strong> Minnesota, 250 Biological Science Center, 1445 Gortner Ave, St. Paul,<br />

MN 55108, USA. dickiei@landcareresearch.co.nz. Ectomycorrhizal fungi <strong>of</strong><br />

North <strong>America</strong>n oak savannas.<br />

Oak savannas, once a dominant ecosystem <strong>of</strong> Midwestern North <strong>America</strong>,<br />

have all but disappeared from the landscape. Although much <strong>of</strong> oak savanna has<br />

been lost to agricultural conversion, other areas have converted to oak woodlands<br />

due to suppression <strong>of</strong> fire. We compare the ectomycorrhizal fungal community <strong>of</strong><br />

Minnesota oak savannas subjected to frequent fire as a restoration tool with former<br />

oak savannas that have converted to oak woodlands due to fire suppression.<br />

Ectomycorrhizal root tip surveys using RFLP analysis and sporocarp collections,<br />

and T-RFLP analysis <strong>of</strong> rhizosphere fungi gave somewhat different views <strong>of</strong><br />

community composition, but all suggest an extremely high diversity <strong>of</strong> fungi in<br />

these systems (estimated at more than 250 species <strong>of</strong> ectomycorrhizal fungi), with<br />

the fungal community broadly dominated by Cenococcum and Russula spp., with<br />

more local dominance by other groups. The high diversity <strong>of</strong> fungi is remarkable,<br />

given the low diversity <strong>of</strong> ectomycorrhizal host plants (three to four species). Although<br />

we predicted that frequent fire might make savanna mycorrhizal communities<br />

more prone to invasion than oak woodland fungal communities, reciprocal<br />

bulk soil transfers between plots had idiosyncratic effects on fungal communities<br />

as measured by T-RFLP. Nonetheless, T-RFLP did distinguish between site differences<br />

and showed similar patterns <strong>of</strong> species dominance as root tip collections.<br />

contributed presentation<br />

Douhan, Greg W. 1 *, Martin, Darren P. 2 and Rizzo, David M. 1 1 Department <strong>of</strong><br />

Plant Pathology, University <strong>of</strong> California, Davis, CA, 9<strong>56</strong>16, USA, 2 Institute <strong>of</strong><br />

Infectious Diseases and Molecular Medicine, University <strong>of</strong> Cape Town, Observatory,<br />

7925, South Africa. gwdouhan@ucdavis.edu. Intragenic recombination<br />

within an actin locus <strong>of</strong> the ectomycorrhizal fungus Cenococcum geophilum.<br />

We have recently detected three divergent lineages <strong>of</strong> Cenococcum<br />

geophilum isolated from a California oak-woodland. One lineage contained two<br />

divergent subclades; within this lineage incongruent phylogenies <strong>of</strong> one mitochondrial<br />

and three nuclear genes suggested potential recombination, but only<br />

when isolates from outside <strong>of</strong> the studied population were included in the analysis.<br />

To further investigate recombination in our local population <strong>of</strong> this putative<br />

asexual fungus, additional loci were sequenced from 44 isolates. Phylogenetic incongruence<br />

between these 10 loci is consistent with recombination occurring<br />

within the local population. However, most <strong>of</strong> the incongruence was caused by<br />

potential recombinant sequence types within the actin locus (~240 bp). Additional<br />

sequence data from the actin locus (~1300 bp) were obtained from parental and<br />

recombinant sequence types. Recombination analyses (RDP, GENECONV,<br />

MAXCHI, CHIMAERA, SISCAN and BOOTSCAN) using the recombination<br />

detection program RDP2 detected intragenic recombination and a potential recombination<br />

breakpoint with the actin locus. However, the divergence between<br />

the two subclades suggests that the recombination event is ancient or was due to<br />

some type <strong>of</strong> horizontal gene transfer or parasexual event. Actin sequence data<br />

from a world-wide sample <strong>of</strong> Cenococcum geophilum may help to differentiate<br />

between these two hypotheses. poster<br />

Douhan, LeAnn I., Andrews, John H., Douhan, Greg W. and Rizzo, David M.<br />

Department <strong>of</strong> Plant Pathology, University <strong>of</strong> California, Davis, CA, 9<strong>56</strong>16,<br />

USA. lidouhan@ucdavis.edu. Phyllosphere fungi associated with bay laurel<br />

trees in California.<br />

Phytophthora ramorum (Pr), causal agent <strong>of</strong> sudden oak death, is an emerging<br />

pathogen in coastal forests <strong>of</strong> CA and OR. Pr is a generalist that also causes<br />

leaf necrosis on many native hosts. In particular, bay laurel (Umbellularia californica)<br />

serves as a foliar host that supports high levels <strong>of</strong> sporulation by Pr and<br />

plays a key role in the spread <strong>of</strong> the pathogen. The presence <strong>of</strong> other leaf colo-<br />

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