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Inoculum 56(4) - Mycological Society of America

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MSA ABSTRACTS<br />

Aaltonen, Ronald E.*, Barrow, Jerry R., Lucero, Mary L., Osuna-Avila, Pedro<br />

and Reyes-Vera, Isaac. USDA-ARS Jornada Experimental Range, Las Cruces,<br />

NM 88003, USA. jbarrow@nmsu.edu. The microscopic identification <strong>of</strong> vertically<br />

transferred symbiotic fungi intrinsically integrated with cells, tissues<br />

and organs <strong>of</strong> host plants.<br />

Dual staining methodology and analysis with light microscopy and scanning<br />

electron microscopy were used to determine the nature and extent <strong>of</strong> symbiotic<br />

fungi with native desert grasses shrubs. Trypan Blue that targets fungal chitin<br />

and sudan IV that targets lipid bodies attached to fungal structures were used to<br />

stain cleared roots and leaves. Trypan blue revealed a densely stained fungal network,<br />

bound to the plasmalema <strong>of</strong> meristematic cells, that were transferred to cells<br />

in culture, tissues and all plant organs. Fungal structures were atypical and were<br />

substantially different than commonly observed fungal structures such as hyphae,<br />

spores, etc. Fungal associations with meristem cells facilitate their distribution and<br />

vertical transfer to all parts <strong>of</strong> the plant, seed and to succeeding generations. Significant<br />

are fungal associations with vascular tissue, photosynthetic cells and with<br />

the stomatal complex and suggests significant plant-fungus interactions within<br />

these critical plant cells. poster<br />

Abdelzaher, Hani M. A. Faculty <strong>of</strong> Science, El-Minia University 61519, Egypt.<br />

abdelzaher@link.net. Biological control <strong>of</strong> damping-<strong>of</strong>f and root rot diseases<br />

<strong>of</strong> soybean caused by Pythium spinosum Sawada var. spinosum using three<br />

rhizosphere species <strong>of</strong> soil fungi.<br />

Pythium spinosum was isolated from rhizosphere soil and rhizoplane <strong>of</strong><br />

healthy and infected soybean roots cultivated in an agricultural field located in<br />

Shahean district, El-Minia city, Egypt in June 2003. Rhizosphere and rhizoplane<br />

myc<strong>of</strong>lora isolated from the same sites were tested for their antagonism toward<br />

Pythium spinosum in agar plates. Among the isolated fungi, Aspergillus sulphureus,<br />

Penicillium islandicum and Paecilomyces variotii were chosen according<br />

to their antagonism on agar plates for experimentation to test their effectiveness<br />

for biological control in either autoclaved or nonsterilized soil. Coating<br />

soybean seeds and roots with spores and mycelia <strong>of</strong> these three antagonists gave<br />

germinating seeds and seedlings a very good protection from root-rot, pre- and<br />

post-emergence damping-<strong>of</strong>f caused by P. spinosum. Applying these biocontrol<br />

agents to autoclaved and nonsterilized soil infested with P. spinosum provided an<br />

excellent way <strong>of</strong> protection. contributed presentation<br />

Abe, Jun-ichi P. University <strong>of</strong> Tsukuba, Graduate School <strong>of</strong> Life and Environmental<br />

Science, 1-1, Tennoudai 1 chome, Tsukuba, Ibaraki 305-8572, Japan. jave@sakura.cc.tsukuba.ac.jp.<br />

An arbuscular mycorrhizal genus in the Ericaceae.<br />

Enkianthus is an ericaceous genus with about 17 spp. <strong>of</strong> shrubs and small<br />

trees, commonly distributed in Japan and southern China. Four Japanese native<br />

species <strong>of</strong> the genus Enkianthus (E. campanulatus, E. cernuus f. rubens, E. perulatus,<br />

E. subsessilis) were examined to determine the mycorrhizal status by comparing<br />

with typical ericoid mycorrhizal roots <strong>of</strong> Rhododendron kaempferi. The<br />

roots <strong>of</strong> all species were collected from trees <strong>of</strong> natural stands or public gardens<br />

and from seedlings <strong>of</strong> E. cernuus f. rubens grown in controlled conditions. These<br />

roots were observed with a compound light microscope and SEM. All examined<br />

roots <strong>of</strong> Enkianthus spp. formed only arbuscular mycorrhiza <strong>of</strong> the Paris-type.<br />

The fine roots <strong>of</strong> these species were usually thicker (approx. 150 µm) than the hair<br />

roots <strong>of</strong> R. kaempferi (approx. 80 µm). Short root hair- like structures with thick<br />

walls (approx. 5 µm) were observed occasionally on the fine roots <strong>of</strong> all<br />

Enkianthus spp. and root hairs were observed in E. subsessilis. Consequently, the<br />

mycorrhizal and root morphology <strong>of</strong> these four species are completely different<br />

from R. kaempferi. This result reveals that at least these four species <strong>of</strong> Enkianthus<br />

seem to be arbuscular mycorrhizal and lack ericoid mycorrhiza. These findings<br />

and the mycorrhizal status <strong>of</strong> the ancient ericaceous species are discussed. contributed<br />

presentation<br />

Aime, M. Catherine. USDA-Agricultural Research Service, Systematic Botany &<br />

Mycology Lab, Beltsville, MD 20705, USA. cathie@nt.ars-grin.gov. Molecular<br />

systematics <strong>of</strong> Uredinales.<br />

Rust fungi (Basidiomycota, Uredinales) consist <strong>of</strong> > 7000 species <strong>of</strong> obligate<br />

plant pathogens that possess some <strong>of</strong> the most complex life cycles in the Eumycota.<br />

Traditionally, phylogenetic inference within the Uredinales has been<br />

hampered by a lack <strong>of</strong> morphological characters and incomplete life cycle and<br />

host-specificity data. The application <strong>of</strong> modern molecular characters to rust systematics<br />

has been limited by several factors, including, to name a few, the inability<br />

to pure culture most rusts or unequivocally separate rust from host cells and<br />

other associated fungi in a specimen. Previous molecular systematic studies <strong>of</strong><br />

rusts have focused on analyses <strong>of</strong> 28S or 18S ribosomal DNA, but current contradictions<br />

in rust systematics, especially in the deeper nodes, have not yet been<br />

resolved. In this study, several genes (including 18S, 28S, and EF1alpha) were examined<br />

across the breadth <strong>of</strong> the Uredinales to resolve systematic conflicts and<br />

provide a framework for the group. It is concluded that morphology alone is a<br />

poor predictor <strong>of</strong> rust relationships at most levels and strict morphology-based<br />

classifications and species-delimitations appear obsolete. Host selection, on the<br />

other hand, has played a significant role in rust evolution. The difficulties and utility<br />

<strong>of</strong> analyzing protein-coding genes vs. rDNA in rust systematics are also discussed.<br />

symposium presentation<br />

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

Aime, M. Catherine 1 * and Henkel, Terry W. 21 USDA-Agricultural Research Service,<br />

Systematic Botany & Mycology Lab, Beltsville, MD 20705, USA, 2 Humboldt<br />

State University, Dept. <strong>of</strong> Biological Sciences, Arcata, CA 95521, USA.<br />

cathie@nt.ars-grin.gov. Strategies for bioinventory: lessons from Guyana.<br />

Bioinventory, the identification and enumeration <strong>of</strong> taxa within a given<br />

area, provides the foundation for numerous biological and ecological studies. Yet<br />

fungal inventories are vastly underrepresented in the literature, and the conduction<br />

<strong>of</strong> such inventories presents a host <strong>of</strong> unique difficulties and problems. Special<br />

problems faced in conducting fungal inventories include deciding at which level<br />

to record units (e.g., fruiting bodies, cultures, and/or environmental sequences);<br />

how to construct significant sampling strategies (e.g. plot studies, transects, and/or<br />

sweeps); and, especially, how to conduct the alpha-taxonomy. We have completed<br />

five years <strong>of</strong> comparative plot studies for fungi in a remote, rain-forested region<br />

<strong>of</strong> west-central Guyana. To date we have documented nearly 1,000 species<br />

or morphospecies <strong>of</strong> macromycetes, both ectomycorrhizal and saprotrophic, and<br />

counted >20,000 fruiting bodies. Yet the most time-consuming aspect <strong>of</strong> this<br />

study is the taxonomy. To date, we have been able to identify and publish less than<br />

10% <strong>of</strong> the Guyanese taxa; > 40% <strong>of</strong> these have been species or genera new to<br />

science. Some ideas for recording, analyzing, and identifying fungal taxa from<br />

previously under-sampled areas will be discussed. symposium presentation<br />

Akamatsu, Y. and Saikawa, Masatoshi*. Department <strong>of</strong> Environmental Science,<br />

Tokyo Gakugei University, Koganei-shi, Tokyo 184-8501, Japan. saikawa@ugakugei.ac.jp.<br />

Giant mycelium by Sommerstorffia spinosa.<br />

Since 1984, Sommerstorffia spinosa was obtained several times from samples<br />

<strong>of</strong> debris floating on the water <strong>of</strong> a fire reservoir located in the campus <strong>of</strong><br />

Tokyo Gakugei University. The species has been known as a rotifer-parasite, to<br />

have the ability to capture the animals with a peg, a distal narrow protuberance <strong>of</strong><br />

hypha, or to parasitize them with a bowling-pin shaped sporeling developed from<br />

an encysted, secondary zoospore. In all the strains reported up to now, each <strong>of</strong> the<br />

isolates finished capturing animals after 3 to 7 times <strong>of</strong> capture by the peg and became<br />

solely to produce zoospores. Thus the mycelium was quite limited in size in<br />

all cases. However, in spring, 2004, we obtained a strain <strong>of</strong> the species, the<br />

mycelium <strong>of</strong> which did not finish capturing rotifers (Lepadella oblonga) and grew<br />

unlimitedly to establish a giant mycelium. At 30 days <strong>of</strong> cultivation under water,<br />

it could be seen with a naked eye, because the size being 0.5-3.0 mm in diameter.<br />

The hyphae (7-9 µm wide) constituting the giant mycelium were empty except<br />

only their distal portion terminated with a peg (6-8 µm long, 3-5 µm wide). After<br />

capturing a rotifer, the peg grew into an endozoic thallus that developed one or<br />

two hyphae externally and transformed itself into a zoosporangium with an evacuation<br />

tube (50-80 µm long, 8-10 µm wide). The primary zoospores encysted at<br />

the mouth <strong>of</strong> the evacuation tube to form a mass <strong>of</strong> cysts (7-9 µm). In normal<br />

strains, each <strong>of</strong> the primary cysts soon produces a secondary zoospore, though the<br />

cyst <strong>of</strong> our strain did not produce it, but lost its content, or, in rare occasion, developed<br />

a sporeling (ca. 17 µm long, 8 µm wide). The giant mycelium <strong>of</strong> our<br />

strain also captured two testaceous rhizopods <strong>of</strong> Cryptodifflugia and Euglypha.<br />

contributed presentation<br />

Almeida-Leñero, Lucia 1 , Ludlow-Wiechers, Beatriz 1 , Geel, Bas van 2 , González,<br />

María C. 3 * and Aptroot, André. 4 1 Dept. Ecología y Rec. Nat, Fac. Ciencias,<br />

UNAM, Mexico DF 04510, 2 IBED, Paleoecology and Landscape Ecology, Univ.<br />

Amsterdam Kruislaan 318, 1098 SM Amsterdam The Netherlands, 3 Inst. Biología,<br />

UNAM, Mexico, 4 Centraalbureau voor Schimmelcultures (CBS), Fungal<br />

Biodiversity Centre, P.O. Box 85167, 3508 AD Utrecht, The Netherlands.<br />

mcgv@ibiologia.unam.mx. Records <strong>of</strong> mid-Holocene fungi from Lake Zempoala,<br />

Central Mexico.<br />

The aim <strong>of</strong> the present study is to describe and illustrate fungal spores<br />

recorded on Zempoala lake at 2800 m altitude. The studied interval is <strong>of</strong> mid-<br />

Holocene age. The lake with submerged aquatical and hydroseral shore vegetation,<br />

lie today in the Abies religiosa dominated forest belt. The samples were prepared<br />

using standard techniques for palynological studies. A number <strong>of</strong> selected<br />

fungal spores have been identified, described and illustrated. Ecological environmental<br />

preferences <strong>of</strong> present fungi are also given. Among the fungi type spores<br />

analysed are 2 basidiospores: Enthorriza (type 527), and Urocystis, 3 ascospores:<br />

Astrosphaeriella, Ustulina, Valsaria, and 10 mitospores: Acrodictys, Antennatula,<br />

Brachydesmiella, Endophragmiella, Monodictys, Trichocladium type 1 and 2,<br />

Papulospora, and Virgatospora. These fungus occur together with pollen elements<br />

that define a landscape <strong>of</strong> forest and a water body. Antennatula confirm an<br />

Abies sp. forest, Acrodictys suggests species <strong>of</strong> Populus sp., Virgatospora <strong>of</strong><br />

broad leaved tree forest, and Ustulina the presence <strong>of</strong> deciduous trees. Enthorriza,<br />

and Trichocladium are evidence <strong>of</strong> freshwater. Environment conditions may be<br />

presumed <strong>of</strong> high air humidity considering the presence <strong>of</strong> decaying plant debris<br />

and soil forming fungi such as Monodictys and Papulospora. The fungi were<br />

recorded for first time in paleoecological studies in Mexico. poster<br />

An, Zhiqiang. Merck Research Laboratories, West Point, PA, USA. Polyketide<br />

synthase genes in the pneumocandin-producing fungus Glarea lozoyensis.<br />

Glarea lozoyensis is the producer <strong>of</strong> pneumocandin B0, a potent inhibitor<br />

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