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ABSTRACTS – Contributed Oral Papers<br />

ECOLOGY, ORGANISMAL BIOLOGY,<br />

and ENVIRONMENTAL SCIENCES<br />

Monday, starting at 9:00 a.m. in WILLOWS 2<br />

114a Flowering Patterns following Tephra Disturbance of<br />

Understory Herbs in Old-growth Subalpine Forest, DON-<br />

ALD ZOBEL 1 and JOSEPH ANTOS 2 ( 1 Botany and Plant<br />

Pathology, <strong>Oregon</strong> State University, Cordley Hall 2082, Corvallis<br />

OR 973<strong>31</strong>; 2 Biology, University of Victoria, PO Box<br />

3020 STN CSC, Victoria, BC, Canada V8W 3N5; zobeld@<br />

science.oregonstate.<strong>edu</strong>).<br />

During succession, flowering allows plants to increase<br />

in density and to spread farther than via vegetative reproduction.<br />

Within a community, species range from those for<br />

which frequent flowering is essential for spread to those that<br />

rarely flower. However, few studies consider the full variation<br />

in flowering within a community. Here we analyze flowering<br />

of understory herbs, using permanent plots in forests<br />

affected by 1980 tephra from Mount St. Helens. Incidence of<br />

flowering in 1980-83, 2000, 2005, and 2010 was related to<br />

environment and species properties using logistic regression.<br />

Flowering varied widely among species, with some<br />

never flowering. Overall, incidence of flowering was greater<br />

in herb-rich sites than in sites with few species, but there was<br />

no overall difference between sites with 4.5 versus 15 cm<br />

tephra. Plants with a graminoid or a deciduous, non-clonal<br />

growth form had the highest incidence of flowering; clonal<br />

deciduous and clonal evergreen plants were intermediate;<br />

non-clonal evergreen plants seldom flowered. Species limited<br />

to forest flowered more consistently than those that also<br />

grow in meadows or in early seral conditions. With time,<br />

incidence of flowering increased for deep tephra, herb-poor<br />

sites, species that also grow in early-seral sites, and those<br />

restricted to forests. Species differed widely in their patterns<br />

of flowering among years and with environment. Incidence<br />

varied among common species from 0% (Xerophyllum<br />

tenax) of the situations in which a species was present to<br />

85% (Tiarella unifoliata). Where flowering occurred, 4 to<br />

19% of shoots flowered.<br />

115 Testing Monophyly and Phylogenetic Relationships of<br />

Smittium (Harpellales) using a Five-Gene Molecular Phylogenetic<br />

Analysis, YAN WANG 1 *, ERIC D TRETTER 1 ,<br />

ERIC M JOHNSON 1 , PRASANNA KANDEL 1 , Robert<br />

W LICHTWARDT 2 , and MERLIN M WHITE 1<br />

( 1 Department of Biological Sciences, Boise State University,<br />

1910 University Drive, Boise, ID 83725; 2 Department<br />

of Ecology & Evolutionary Biology, University of Kansas,<br />

1200 Sunnyside Avenue, Haworth Hall, Lawrence, KS<br />

66045; Yanwang@u.boisestate.<strong>edu</strong>).<br />

Smittium is a ubiquitous group of fungi, best known<br />

as endosymbionts of various Arthropods, thus commonly<br />

referred to as the gut fungi. During the 75 years since the<br />

first species, Smittium arvernense, was described, Smittium<br />

has grown to include 81 species. The symbiotic relationships<br />

within this genus range from commensalism, mutualism,<br />

to parasitism. This genus has also helped to advance<br />

our understanding of the gut fungi, by serving as a “model”<br />

for laboratory studies of the fungal trichomycetes. Many<br />

isolates of Smittium have been used for host feeding, isozyme,<br />

physiological, serological, ultrastructural, and now<br />

ongoing molecular systematic studies. Previous and recent<br />

molecular studies have shown that Smittium is polyphyletic<br />

but with consistent separation of Smittium culisetae, one of<br />

the most common and widespread species, from the remainder<br />

of Smittium species. Here we used morphological (sexual<br />

and asexual spores shape), molecular (18S and 28S rRNA<br />

genes), immunological, and isozyme evidence to suggest a<br />

new genus, Zancudomyces, to accommodate Smittium culisetae.<br />

A multi-gene dataset, consisting of 18S and 28S rRNA<br />

genes, as well as RPB1, RPB2, and MCM7 translated protein<br />

sequences for Smittium and related Harpellales (Austrosmittium,<br />

Coleopteromyces, Furculomyces, Pseudoharpella,<br />

Stachylina and Trichozygospora), was used for phylogenetic<br />

analyses to test the monophyly of Smittium. A consensus<br />

tree was generated with strong support at multiple levels.<br />

The clades and branches of the tree were assessed relative<br />

to morphological traits for the taxa of interest, including<br />

holdfast shape, thallus branching type, trichospore (asexual<br />

spore) and zygospores (sexual spore) characters as an aid to<br />

inform the taxonomy and eventual systematic revisions and<br />

reclassification. A narrower genus definition of Smittium was<br />

supported by molecular data, and approved by morphological<br />

reexamination.<br />

116 Investigating the Presence and Impacts of Wolbachia,<br />

a Bacterial Symbiont, on a Threatened Butterfly, AMY<br />

TRUITT* and CATHERINE De RIVERA (Department<br />

of Environmental Science and Management, Portland State<br />

University, 1825 SW Broadway, Portland, OR 97201; amtruitt@pdx.<strong>edu</strong>).<br />

The endosymbiotic bacteria, Wolbachia, likely affect<br />

population dynamics of the imperiled <strong>Oregon</strong> silverspot butterfly,<br />

(Speyeria zerene hippolyta, OSB) and may have been<br />

a contributor in the decline of its many extirpated populations.<br />

Some strains of Wolbachia induce cytoplasmic incompatibility<br />

between its host insects and uninfected conspecifics,<br />

including for many Lepidoptera. The goals of this study<br />

were to determine: if this species is infected with Wolbachia,<br />

whether infection affects population growth of this butterfly.<br />

We conducted a screen for Wolbachia infection by collecting<br />

samples from archived female butterflies (from 1999<br />

and 2001-2011, n=234), extracting DNA from the samples,<br />

and employing polymerase chain reaction protocols using<br />

Wolbachia-specific primers. Reproduction data, eggs laid<br />

and eggs hatched, for infected versus uninfected individuals<br />

were analyzed. Proportion of infected individuals per year<br />

was compared to population indices.<br />

81

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