Inoculum 56(4) - Mycological Society of America
Inoculum 56(4) - Mycological Society of America
Inoculum 56(4) - Mycological Society of America
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Matheny, P. Brandon Dept. <strong>of</strong> Biology, Clark University, Worcester MA 01610,<br />
USA. pmatheny@clarku.edu. Phylogeography <strong>of</strong> the Inocybaceae (euagarics):<br />
evidence for multiple biogeographic hypotheses.<br />
The Inocybaceae, a species-rich family <strong>of</strong> ectomycorrhizal euagarics, is distributed<br />
world-wide in various ectotrophic habitats and phylogenetically is one <strong>of</strong><br />
the more well-studied clades <strong>of</strong> euagarics. As a result, the group represents an excellent<br />
model for phylogeographic research <strong>of</strong> ectomycorrhizal fungi. Area optimization<br />
cladograms using a parsimony method support relatively recent dispersal<br />
events to tropical and temperate South <strong>America</strong> and to New Zealand.<br />
Extinctions are minimized under this scenario. In contrast, accomodating ancient<br />
vicariance events and allowing for no dispersal must account for many extinctions,<br />
which proves to be a less parsimonious explanation for the current distribution<br />
<strong>of</strong> the family. However, tropical and southern hemisphere taxa express a<br />
strong degree <strong>of</strong> species-level and higher-level endemism and vicariance cannot<br />
be ruled out in all cases. Endemic taxa include many Australian, African, and<br />
South <strong>America</strong>n species and higher-level groups. In contrast, some north temperate<br />
species are believed to be wide-spread geographically across Asia, Europe,<br />
and North <strong>America</strong>. Phylogeographic relationships <strong>of</strong> South <strong>America</strong>n and Australian<br />
taxa are heterogeneous. For exmple, a South <strong>America</strong>n Noth<strong>of</strong>agus associate<br />
is basal to a north temperate Pinaceae-associated clade, but another Noth<strong>of</strong>agus<br />
associate is related to Australian Myrtaceae symbionts. In addition, a new<br />
genus, Auritella, is proposed to accomodate African and Australian lineages with<br />
elongated cheilocystidia, necropigmented basidia, and/or evolution <strong>of</strong> a sequestrate<br />
habit. Molecular clock dating techniques using nLSU-rDNA and rpb2 genes<br />
suggest a late Cretaceous split (about 90 Mya) between the African and Australian<br />
clades <strong>of</strong> Auritella. Recent dispersal between these two continents for this genus<br />
is firmly rejected. symposium presentation<br />
Matheny, P. Brandon 1 *, Aime, M. Catherine 2 , Ammirati, Joseph F. 3 , Aoki, T. 4 ,<br />
Baroni, Timothy J. 5 , Binder, M. 1 , Crane, Patricia E. 6 , Curtis, J. 1 , de Nitis, M. 1 ,<br />
Dentinger, Bryn C. 6 , Frøslev, T. 8 , Ge, Z.W. 9 , Halling, Roy 10 , Hosaka, K. 11 , Hughes,<br />
Karen W. 12 , Kerrigan, Richard W. 13 , Kropp, Bradley R. 14 , Langer, G.E. 15 , Matsuura<br />
K. 16 , McLaughlin David J. 6 , Nilsson R.H. 17 , Nishida H. 18 , Padamsee M. 6 ,<br />
Petersen Ronald H. 12 , Piepenbring, M. 19 , Seidl, Michelle T. 3 , Slot, Jason 1 , Vauras,<br />
J. 20 , Vellinga, E.C. 21 , Wang, Zheng 1 , Wilson, A. 1 , Yang, Z.L 9 , and Hibbett, David<br />
S. 1 . 1 Biology Dept., Clark Univ., 950 Main St., Worcester, MA 01610 USA; 2 Systematic<br />
Botany & Mycology Lab, 10300 Baltimore Ave., Beltsville, MD 20705-<br />
2350 USA; 3 Biology Dept., Box 351330, Univ. <strong>of</strong> Washington, Seattle, WA USA<br />
98195; 4 National Inst. Agrobiological Sciences, Kannondai 2-1-2, Tsukuba,<br />
Ibaraki 305-8602, Japan; 5 Dept. Biological Sciences, Box 2000, State Univ. New<br />
York - College at Cortland, Cortland, NY 13045 USA; 6 Dept. Plant Biology,<br />
Univ. <strong>of</strong> Minnesota, St. Paul, MN 55108-1095 USA; 7 Northern Forestry Centre,<br />
Canadian Forest Service, 5320 - 122 Street, Edmonton, AB Canada T6H 3S5;<br />
8 Botanical Inst., Univ. <strong>of</strong> Copenhagen, Øster Farimagsgade 2D, DK-1353 Copenhagen,<br />
Denmark; 9 Kunming Inst. Botany, Chinese Academy <strong>of</strong> Sciences, Heilongtan,<br />
Kunming 650204, P. R. China; 10 Inst. Systematic Botany, The New York<br />
Botanical Garden, Bronx, NY 10458-5126 USA; 11 Dept. Botany & Plant Pathology,<br />
Oregon State Univ., Corvallis, OR 97331; 12 Botany Dept., Univ. <strong>of</strong> Tennessee,<br />
Knoxville, TN 37996-1100; 13 Sylvan Research, 198 Nolte Dr., Kittanning,<br />
PA 16201 USA; 14 Dept. Biology, Utah St. Univ., Logan, UT 84322 USA;<br />
15 Univ. Kassel, FB 18 Naturwissenschaften, FG Oekologie, Heinrich-Plett-Str.<br />
40, D-34132 Kassel; 16 Dept. Organismic & Evol. Biology, Harvard Univ., 26 Oxford<br />
St., Cambridge, MA 02138 USA; 17 Göeteborg Univ., Botaniska Inst., Box<br />
460, SE 405 30 Göeteborg, Sweden; 18 Inst. Molecular & Cellular Biosciences,<br />
Univ. Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan; 19 Botanisches<br />
Inst., J. W. Göethe-Univ., Senckenberganlage 31-33, D-60054 Frankfurt;<br />
20 Herbarium, Biology Dept., Univ. <strong>of</strong> Turku, SF-20500 Turku, Finland; 21 Plant &<br />
Microbial Biol. Dept., Univ. <strong>of</strong> California at Berkeley, 111 Koshland Hall, Berkeley,<br />
CA 94720-3102 USA. pmatheny@clarku.edu. Progress towards assembling<br />
the tree <strong>of</strong> life for the Basidiomycota.<br />
The phylogeny <strong>of</strong> the Basidiomycota has been addressed in a limited way<br />
from analysis <strong>of</strong> nucleotide data. Most studies have relied primarily on single gene<br />
analyses <strong>of</strong> nuclear ribosomal RNA genes (18S or 25S). Confidence measures<br />
have been generally inadequate in such studies despite efforts at dense taxon sampling.<br />
As part <strong>of</strong> the the Assembling the Fungal Tree <strong>of</strong> Life (AFTOL) project,<br />
our laboratory is generating multi-locus datasets for resolving higher-level phylogenetic<br />
relationships <strong>of</strong> Basidiomycota. We present results from a nuclear rDNA<br />
data set (3.5 kb) for 200 AFTOL basidiomycetes, a protein-coding data set <strong>of</strong><br />
rpb2, rpb1, and tef1 (1350 amino acids) for 85 taxa, and a combination <strong>of</strong> these<br />
data into a 6-locus data set (18S, 25S, 5.8S, rpb2, rpb1, and tef1). rDNA sequences<br />
support a sister relationship between the Ustilaginomycetes (true smut<br />
fungi) and the Hymenomycetes (mushroom-forming fungi), a relationship consistent<br />
with several ultrustructural and biochemical characters. However, a combination<br />
<strong>of</strong> rDNA and protein-coding genes suggests the Urediniomycetes (rusts<br />
and allies) could be the sister group to the Hymenomycetes. Spliceosomal intron<br />
placement might support this view. The Microbotrymycetidae (a diverse group including<br />
anther smuts and diverse yeasts) appears sister to the Urediniomycetidae<br />
with strong measures <strong>of</strong> support. rDNA Bayesian and rpb2 parsimony analyses,<br />
however, fail to support the monophyly <strong>of</strong> the Exobasidiomycetidae. Basal nodes<br />
in the Hymenomycetes are well-resolved and moderately supported in the most<br />
MSA ABSTRACTS<br />
gene-rich data sets. In the 6-locus data set, the cantharelloid clade represents the<br />
most ancient branch among the Homobasidiomycetes. The trechisporoid and<br />
gomphoid-phalloid clades represent a monophyletic group with moderately high<br />
bootstrap support. Distal homobasidiomycete clades also receive moderate to<br />
high bootstrap support. Examples include: the inclusive monophyly <strong>of</strong> the athelioid<br />
and bolete clades; the sister position <strong>of</strong> the russuloid clade to the euagarics,<br />
atheloid, and bolete clades; and a sister relationship between the thelephoroid and<br />
polyporoid clades. contributed presentation<br />
Matsuda, Yosuke*, Noguchi, Yuuta, Nakanishi, Kenichi and Ito, Shin-ichiro.<br />
Laboratory <strong>of</strong> Forest Pathology and Mycology, Faculty <strong>of</strong> Bioresource Sciences,<br />
Mie University, Tsu 514-8105, Mie, Japan. m-yosuke@bio.mie-u.ac.jp. Ectomycorrhizal<br />
associations <strong>of</strong> naturally grown Pinus thunbergii seedlings in a<br />
coastal pine forest.<br />
To identify ectomycorrhizal (ECM) fungi associated with naturally regenerated<br />
Pinus thunbergii seedlings grown at coastal areas, we sampled 15 currentyear-old<br />
and 14 more than 1-year-old seedlings at a coastal pine stand. ECM roots<br />
were first morphotyped by microscopy, and were then classified as RFLP-types<br />
analyzing the rDNA <strong>of</strong> the internal transcribed spacer region digested with two<br />
enzymes, Alu I and Hin f I. RFLP-types were directly sequenced to identify fungal<br />
species. In total, 13 species were found and Cenococcum geophilum was identified<br />
morphologically. For current- and more than 1-year-old seedlings, C.<br />
geophilum and Lactarius sp. were either the most or the second most dominant<br />
species in terms <strong>of</strong> both the number <strong>of</strong> ECM roots and the frequency <strong>of</strong> occurrences<br />
per seedling. The number <strong>of</strong> ECM roots colonized by C. geophilum or Lactarius<br />
sp. was positively correlated with the shoot dry weight <strong>of</strong> seedlings, and the<br />
correlation coefficient <strong>of</strong> the latter species was higher than that <strong>of</strong> the former.<br />
These results indicate that multiple species <strong>of</strong> ECM fungi are involved in the<br />
ECM formation on P. thunbergii seedlings and a few dominant species may be<br />
important for the growth and survival <strong>of</strong> the seedlings at the coastal area. poster<br />
Matsumoto, Naoyuki 1 * and Hoshino, Tamotsu 2 . 1 National Institute for Agro-Environmental<br />
Sciences, Tsukuba 305-8267, Japan, 2 National Institute <strong>of</strong> Advanced<br />
Industrial Science and Technology (AIST), Sapporo 062-8517, Japan. nowmat@affrc.go.jp.<br />
Adaptations <strong>of</strong> snow mold fungi, Typhula ishikariensis and<br />
T. incarnata, to diverse winter climates.<br />
Typhula ishikariensis consists <strong>of</strong> two biological species, each including several<br />
endemic taxa adapted to local environments. Freezing tolerance <strong>of</strong> mycelia at<br />
–20C is a common trait in some taxa <strong>of</strong> both biological species existing in<br />
Moscow, Saskatchewan, and coastal regions in north Norway and Greenland.<br />
Their growth at 10 to 12 C becomes irregular due presumably to high respiration<br />
because free radical scavengers improve growth. Such a trait coincides with DNA<br />
sequence in the large mitochondrial subunit. T. ishikariensis biotype B is distributed<br />
in localities differing in the number <strong>of</strong> days with snow cover ranging from<br />
40 to 150 days p.a. Its sclerotia become smaller and virulence increases with decreasing<br />
snow cover days. The population in the least snowy locality is practically<br />
soilborne and seldom develops sporocarps. Soil environment is more stable<br />
than the habitat under snow cover in such a changeable habitat. T. incarnata populations<br />
from diverse localities are similar in sclerotium size as well as in virulence:<br />
a single isolate <strong>of</strong> T. incarnata covers a broad variation in sclerotium size<br />
comparable to that in the T. ishikariensis complex. They, however, differ in the<br />
number <strong>of</strong> days required for carpogenic sclerotium germination. In the less snowy<br />
habitats, when persistent snow cover starts is difficult to predict. Populations in<br />
such a habitat are “prudent” in this respect. symposium presentation<br />
Matsuura, Kenji. Laboratory <strong>of</strong> Insect Ecology, Graduate School <strong>of</strong> Environmental<br />
Science, Okayama University, 1-1-1 Tsushima-naka, Okayama 700-8530,<br />
Japan. kenjiJPN@cc.okayama-u.ac.jp. Termites and a termite-egg-mimicking<br />
fungus: a novel insect-fungus interaction.<br />
Mimicry has evolved in a wide range <strong>of</strong> organisms encompassing diverse<br />
tactics for defense, foraging, pollination, and social parasitism. Egg protection is<br />
an essential behavior in social animals. Here I report an extraordinary case <strong>of</strong> egg<br />
mimicry by a fungus, whereby the fungus gains competitor-free habitat in termite<br />
nests. The phenomenon <strong>of</strong> termites harboring brown fungal balls alongside their<br />
eggs was found recently in the Japanese termite Reticulitermes speratus. When<br />
workers recognize the eggs laid by queens, they bring the eggs together and heap<br />
them up in order to take care <strong>of</strong> them. Brown fungal balls, named “termite balls,”<br />
are frequently found in egg piles <strong>of</strong> Reticulitermes termites in Japan and the US.<br />
The brown ball was identified as the sclerotium <strong>of</strong> a corticioid fungus, Fibularhizoctonia<br />
sp. nov. Although termite balls promote egg survival under certain experimental<br />
conditions, the relationship is not always symbiotic but is sometimes<br />
parasitic or pathogenic. Dummy-egg bioassays using glass beads showed that<br />
both morphological and chemical camouflage were necessary to induce tending<br />
by termites. Scanning electron microscopic observation revealed sophisticated<br />
mimicry <strong>of</strong> the smooth surface texture. These results provide clear evidence that<br />
termite balls mimic termite eggs. This finding suggests that mimicry is a diverse<br />
and widespread tactic even in fungi. symposium presentation<br />
Continued on following page<br />
<strong>Inoculum</strong> <strong>56</strong>(4), November 2005 39