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<title>Theses and Dissertations (Botany and Plant Pathology)</title>
<link>http://hdl.handle.net/1957/17954</link>
<description/>
<items>
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<rdf:li rdf:resource="http://hdl.handle.net/1957/38181"/>
<rdf:li rdf:resource="http://hdl.handle.net/1957/37709"/>
<rdf:li rdf:resource="http://hdl.handle.net/1957/37609"/>
<rdf:li rdf:resource="http://hdl.handle.net/1957/37339"/>
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</items>
<dc:date>2013-06-19T19:21:23Z</dc:date>
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<item rdf:about="http://hdl.handle.net/1957/38181">
<title>Fungal endophyte diversity in foliage of native and cultivated Rhododendron species determined by culturing, ITS sequencing, and pyrosequencing</title>
<link>http://hdl.handle.net/1957/38181</link>
<description>Fungal endophyte diversity in foliage of native and cultivated Rhododendron species determined by culturing, ITS sequencing, and pyrosequencing
Raizen, Nathaniel L.
Western Oregon is home to native Rhododendron species and is the center for cultivated&#13;
Rhododendron production in the United States. These Rhododendron spp. are known to&#13;
be infected with fungal endophytes. However, the community structure of these&#13;
endophytes in native and cultivated Rhododendron is poorly understood. Our study&#13;
targeted the foliar fungal endophyte communities of two native Rhododendron spp. and&#13;
two non-native commercially cultivated Rhododendron varieties. Parallel culturedependent&#13;
(fungal isolation and identification based on ITS sequencing) and cultureindependent&#13;
sequencing approaches (metagenomic sequencing of the ITS region using&#13;
454 pyrosequencing) were employed, and results provided evidence of distinctly different&#13;
community structure in each host species. Additionally, results indicated higher diversity&#13;
among cultivated and nursery grown Rhododendron. This suggests that the close&#13;
proximity of the nurseries sampled to the forest environment allows exposure to two&#13;
distinct sources of endophyte infection. Together, our results show the importance of host&#13;
identity and environment in structuring the associated endophyte communities.
Graduation date: 2013
</description>
<dc:date>2013-03-21T00:00:00Z</dc:date>
</item>
<item rdf:about="http://hdl.handle.net/1957/37709">
<title>Organic pesticide modification of the species interactions in an annual plant community</title>
<link>http://hdl.handle.net/1957/37709</link>
<description>Organic pesticide modification of the species interactions in an annual plant community
Pfleeger, Thomas G.
Graduation date: 1991
</description>
<dc:date>1990-10-12T00:00:00Z</dc:date>
</item>
<item rdf:about="http://hdl.handle.net/1957/37609">
<title>Population dynamics, extraction, and response to nematicide of three plant parasitic nematodes on peppermint (mentha piperita L.)</title>
<link>http://hdl.handle.net/1957/37609</link>
<description>Population dynamics, extraction, and response to nematicide of three plant parasitic nematodes on peppermint (mentha piperita L.)
Merrifield, Kathryn J.
The efficiencies of wet sieving/sucrose&#13;
centrifugation (WS/SC) recovery of Pratylenchus penetrans&#13;
(59 %), Paratylenchus sp., (80 %), and Criconemella&#13;
xenoplax (66 %) were established. Baermann funnels (BF)&#13;
recovered significantly more P. penetrans (p = 0.01) and&#13;
significantly less (p = 0.01) C. xenoplax than did WS/SC.&#13;
While densities of P. penetrans in stored soil remained&#13;
constant over the three days following field sample&#13;
collection, Paratylenchus sp. and C. xenoplax densities&#13;
increased significantly on the second day and decreased to&#13;
their original level on the third day. During mist&#13;
chamber extraction, P. penetrans continued to emerge from&#13;
peppermint root tissue for 38 days, but 90 % of the total&#13;
was recovered after 10 days.&#13;
The standard core, consisting of 500 g dry soil plus&#13;
the roots and rhizomes in that soil, was developed to&#13;
express endoparasitic and ectoparasitic nematode densities&#13;
in peppermint field soil, roots, and rhizomes.&#13;
Enumerating nematode densities within the different plantsoil&#13;
components of a particular volume of soil more&#13;
closely describes the total nematode population pressure&#13;
on the plant growing in that volume of soil. Therefore,&#13;
endoparasitic nematode population levels were expressed as&#13;
numbers in standard core soil, roots, rhizomes, or total&#13;
core (soil, root, and rhizome populations combined).&#13;
P. penetrans populations in peppermint fields peaked&#13;
in early May, decreased through the summer, peaked again&#13;
in August, and decreased through the fall to a low winter&#13;
level. Peaks in the P. penetrans population followed&#13;
peppermint root weight peaks by 3 to 6 wks. Paratylenchus&#13;
sp. populations remained at relatively low levels&#13;
throughout the year except for a pronounced peak in&#13;
August, which followed the root weight peak by 3 to 6 wks.&#13;
The C. xenoplax population also peaked 3 to 6 wks after&#13;
the August root weight peak but fluctuated markedly&#13;
throughout the remainder of the year. From 70 to 90 % of&#13;
the total P. penetrans population was in roots in early&#13;
May, decreased to 40 to 50 % by late June and 20 to 40 %&#13;
in August. Up to 20 % of the population was in rhizomes&#13;
on some dates, but the rhizome percentage was usually less&#13;
than 10. Fewer P. penetrans were recovered from rhizomes&#13;
during the harsh winter of 1988-89 than during the mild&#13;
winter of 1989-90.&#13;
Analysis of point samples (pretreatment,&#13;
posttreatment, and harvest samples) and area under&#13;
nematode population curves (AUNPC) were used to compare&#13;
nematode populations in oxamyl-treated (1.1 kg a.i./ha)&#13;
and nontreated plots in two peppermint fields through the&#13;
two growing seasons. Point sample analyses detected&#13;
significant decreases in treated soil, root, and total&#13;
standard core P. benetrans populations compared to&#13;
nontreated populations in several pretreatment and harvest&#13;
sample dates and in two rhizome harvest sample dates. No&#13;
treatment differences were observed in Paratylenchus sp.&#13;
or C. xenoplax populations using this analysis. AUNPC&#13;
analysis detected significant decreases in several treated&#13;
root and rhizome P. penetrans populations compared to&#13;
nontreated populations and in total core populations in&#13;
field 1 during one growing season and in field 2 during&#13;
two growing seasons. Significant decreases in C. xenoplax&#13;
populations were observed in one field during one growing&#13;
season.&#13;
Peppermint hay weight was significantly greater in&#13;
treated than in nontreated plots in one of three fields in&#13;
1988 and in one of three fields during 1989. Oil in ml/kg&#13;
fresh hay weight was significantly lower in treated than&#13;
in nontreated plots in one of three fields during 1989.&#13;
No treatment differences were detected in milliliters of&#13;
oil distilled from 2m² field area.&#13;
Peppermint oil production is the final measure of a&#13;
treatment from a mint grower's perspective. Because&#13;
oxamyl had no effect on mint oil production, AUNPC appears&#13;
to be a better measure of parasitic nematode pressure on&#13;
peppermint, since this method of analysis detected fewer&#13;
significant differences between nematode populations&#13;
between treated and non-treated plots.
Graduation date: 1991
</description>
<dc:date>1990-06-04T00:00:00Z</dc:date>
</item>
<item rdf:about="http://hdl.handle.net/1957/37339">
<title>Effect of wheat cultivar mixtures on populations of Puccinia striiformis races</title>
<link>http://hdl.handle.net/1957/37339</link>
<description>Effect of wheat cultivar mixtures on populations of Puccinia striiformis races
DiLeone, Julie A.
This study quantified the frequency of simple versus&#13;
complex races of Puccinia striiformis Westend. in mixtures&#13;
of wheat cultivars possessing different race-specific&#13;
resistance genes. A simple race of a pathogen can infect&#13;
only one component, and a complex race of the pathogen can&#13;
infect two or more components of an intraspecific plant&#13;
mixture. The treatments were designed so that the race that&#13;
was complex changed depending on the host mixture, thus&#13;
enabling us to observe the influence of pathogen complexity&#13;
in different host genetic backgrounds. Six cultivar&#13;
mixtures and one pure stand of winter wheat were inoculated&#13;
with three races of P. striiformis (CDL 27, CDL 29, and CDL&#13;
41) at two locations for two seasons. Potted plants of&#13;
three winter wheat cultivars (Paha, Tres, and Tyee) that&#13;
were each susceptible to one of the three races of the&#13;
pathogen were used to sample the pathogen during the field&#13;
epidemics. Disease incidence on the differential cultivars&#13;
was used to calculate the proportion of the three races in&#13;
each treatment. The specific cultivars included in the&#13;
mixtures influenced the frequencies of the three races.&#13;
Increasing the number of virulent races in a mixture reduced&#13;
the frequency of the complex race relative to the other two&#13;
races. When two of the races (races 29 and 41) were complex&#13;
on the same mixture, location had an effect on which of the&#13;
races was more frequent. When race 29 was the complex race&#13;
in the mixture, it was more frequent than when race 41 was&#13;
the complex race. The results suggest that environmental&#13;
interactions, genetic background of the pathogen race, host&#13;
composition, and interaction among pathogen races may be as&#13;
important in determining race frequencies in mixtures as is&#13;
stabilizing selection sensu Vanderplank (1968).
Graduation date: 1993
</description>
<dc:date>1993-01-28T00:00:00Z</dc:date>
</item>
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