<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns="http://www.w3.org/2005/Atom">
<title>Distinguished Graduates (Fisheries and Wildlife)</title>
<link href="http://hdl.handle.net/1957/17094" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/1957/17094</id>
<updated>2013-05-26T00:51:27Z</updated>
<dc:date>2013-05-26T00:51:27Z</dc:date>
<entry>
<title>Predator-prey interactions under the influence of ammonia</title>
<link href="http://hdl.handle.net/1957/17991" rel="alternate"/>
<author>
<name>Woltering, Daniel Mark</name>
</author>
<id>http://hdl.handle.net/1957/17991</id>
<updated>2011-03-24T07:09:19Z</updated>
<published>1976-04-09T00:00:00Z</published>
<summary type="text">Predator-prey interactions under the influence of ammonia
Woltering, Daniel Mark
Predator-prey interactions, as measured by the consumption&#13;
and growth rates of a predator (Micropterus salmoides) and by the&#13;
observed activities of both predator and prey (Gambusia affinis),&#13;
were found to be sensitive to sublethal levels of ammonium chloride&#13;
(reported as unionized ammonia NH₃).&#13;
One bass and 15, 30, 60 or 120 mosquitofish were placed in&#13;
each of 13 150 liter aquaria, designed with uniform cover for the&#13;
prey, and allowed to interact for ten days. These prey densities&#13;
were maintained by restocking every 24 hours, thus providing a wide&#13;
range of food availability for the predators. Experiments were first&#13;
run without adding ammonium chloride in order to establish baseline&#13;
responses of both predators and prey. The system was then exposed&#13;
to a range of toxicant concentrations from 0.13 mg/l to 0.86 mg/1&#13;
NH₃. Responses of predators and prey were measured and compared&#13;
to the baseline data. Consumption and growth rates of the unexposed bass increased&#13;
with increasing prey densities. Consumption rates ranged from one&#13;
to ten percent of mean dry weight of bass per day, growth rates from&#13;
a loss of two percent to a gain of three and one-half percent of mean&#13;
dry weight of bass per day. Exposure to low levels of NH₃&#13;
had no&#13;
observable effect on the interactions. When exposed to toxicant concentrations&#13;
higher than 0.34 mg/l NH₃, substantial decreases in&#13;
consumption and growth rates were found for bass in experiments&#13;
with prey densities above 15. These deviations from the baseline&#13;
correlated well with prey density in that the effects were greatest at&#13;
high prey densities where the bass were being continuously harassed&#13;
by the mosquitofish. The utility of this type of bioassay approach to&#13;
aquatic pollution is discussed.
Graduation date: 1976
</summary>
<dc:date>1976-04-09T00:00:00Z</dc:date>
</entry>
<entry>
<title>The dynamics of exploited guppy populations exposed to dieldrin</title>
<link href="http://hdl.handle.net/1957/17990" rel="alternate"/>
<author>
<name>Liss, William J.</name>
</author>
<id>http://hdl.handle.net/1957/17990</id>
<updated>2011-03-24T07:09:19Z</updated>
<published>1974-03-11T00:00:00Z</published>
<summary type="text">The dynamics of exploited guppy populations exposed to dieldrin
Liss, William J.
Sixteen populations of guppies (Poecilia reticulata) were established&#13;
in laboratory aquariums. Eight populations were exposed to&#13;
dieldrin at a mean concentration of 0.525 ppb in the water and 2.11&#13;
ppm in the food, tubificid worms. Eight populations received control&#13;
water and food. All populations were fed three grams of tubificid&#13;
worms per day.&#13;
Exploitation rates of 0.60, 0.45, 0.30, and 0.15 were selected.&#13;
Each rate was assigned to two control populations and two populations&#13;
exposed to dieldrin. All fish except the young (less than nine millimeters)&#13;
in each population were exploited at their designated rate&#13;
according to a systematic exploitation schedule every 28 days. All&#13;
populations were exploited fifteen times.&#13;
The number of fish in the exploited phase of populations exploited&#13;
at 0.60 remained stable during most of the experiment. Populations&#13;
exposed to dieldrin maintained a greater number of fish than control populations through increased recruitment. Apparently, dieldrin reduced&#13;
the cannibalistic behavior of adult guppies and allowed more&#13;
young to survive to recruitment size. The biomass and yield in weight&#13;
of control populations and populations exposed to dieldrin was similar.&#13;
Increased recruitment in populations exposed to dieldrin was therefore&#13;
compensated by reduced growth.&#13;
Reductions in recruitment resulting from increased cannibalism&#13;
on young fish caused the number of fish in the exploited phase of&#13;
populations exploited at 0. 45, 0. 30, and 0. 15 to decline. Populations&#13;
exposed to dieldrin maintained the same number of fish and followed&#13;
the same trends as control populations. These populations maintained&#13;
a high density of adult fish and intraspecific competition for food may&#13;
have overcome the tendency of dieldrin to reduce cannibalistic behavior.&#13;
Although population number declined, the biomass and yield in&#13;
weight of these populations remained stable. Reductions in recruitment&#13;
had not yet caused a major decline in the number of adults and&#13;
may have been compensated by increased fish growth. As population&#13;
number declined, the average length and weight of the catch increased.&#13;
Populations exploited at 0. 45, 0. 30, and 0. 15 were apparently beginning&#13;
to undergo periodic cycles.&#13;
Mean equilibrium yield in weight declined as exploitation rate&#13;
was reduced. Yield in weight of each population was located on the&#13;
descending limb of a surplus-yield curve. Age, growth, production, and yield in weight of females in&#13;
populations exploited at 0.60, 0. 45, and 0.30 were determined from the&#13;
length-frequency distributions of the catch. At each exploitation rate,&#13;
during the younger age classes, when the production of a cohort of&#13;
females was greater than its yield, the biomass of the cohort increased.&#13;
During the older age classes, when yield became greater than production,&#13;
the biomass of the cohort declined.&#13;
As exploitation rate increased, the mean individual weight of&#13;
each age class and the relative growth rate of fish of a particular&#13;
weight also increased. Increased growth enabled fish from high exploitation&#13;
rates to maintain greater production and yield than fish&#13;
from low exploitation rates.
Graduation date: 1974
</summary>
<dc:date>1974-03-11T00:00:00Z</dc:date>
</entry>
<entry>
<title>Habitat utilization of the pileated woodpecker, Blue Mountains, Oregon</title>
<link href="http://hdl.handle.net/1957/17989" rel="alternate"/>
<author>
<name>Bull, Evelyn L.</name>
</author>
<id>http://hdl.handle.net/1957/17989</id>
<updated>2011-03-24T07:09:20Z</updated>
<published>1975-02-24T00:00:00Z</published>
<summary type="text">Habitat utilization of the pileated woodpecker, Blue Mountains, Oregon
Bull, Evelyn L.
In the spring and summer of 1973 and 1974 a study of&#13;
habitat utilization by pileated woodpeckers (DryocoPus&#13;
pileatus picinus) was conducted on the Starkey Experimental&#13;
Forest and Range in the Blue Mountains of northeastern&#13;
Oregon.&#13;
Pileated woodpeckers are dependent on a forest habitat&#13;
for feeding and nesting. The alteration of this habitat&#13;
through intensive timber management is detrimental&#13;
to the species, particularly because of the elimination&#13;
of dead wood, both standing and downed.&#13;
Nests were excavated in large ( &gt;58 cm dbh), tall&#13;
(&gt;12m), ponderosa pine (Pinus ponderosa) and larch&#13;
(Larix occidentalis) snags in areas with mean densities of 494 stems and 50 snags per ha. These nest trees were&#13;
in forest sites containing the highest densities of stems&#13;
and snags found on the study area.&#13;
Pileated woodpeckers fed primarily in dead wood in&#13;
snags, logs, and naturally created stumps. Feeding occurred&#13;
in a variety of tree species of various sizes and&#13;
physical characteristics. Forest sites containing the&#13;
highest densities of stems and snags on the study area&#13;
were preferred by the pileated woodpecker for feeding.&#13;
In 1974, there were at least 13 pairs of pileated&#13;
woodpeckers on the 11,400 ha study area. This translated&#13;
to 665 ha of forested habitat per pair. During spring&#13;
and summer, nesting territories were estimated at 250 to&#13;
500 ha.&#13;
The critical components in pileated woodpecker habitat&#13;
are: snags, particularly large snags, logs, large&#13;
trees, diseased trees, dense timber, and high densities&#13;
of snags. The requisite attributes of size, density,&#13;
and decadent trees are most common in mature uncut&#13;
forests. These elements can be maintained at a satisfactory&#13;
level with moderate modifications of current&#13;
forest management practices.
Graduation date: 1975
</summary>
<dc:date>1975-02-24T00:00:00Z</dc:date>
</entry>
<entry>
<title>Evaluation of wire fences for control of coyote depredations</title>
<link href="http://hdl.handle.net/1957/17988" rel="alternate"/>
<author>
<name>Thompson, Bruce Carlyle</name>
</author>
<id>http://hdl.handle.net/1957/17988</id>
<updated>2011-03-24T07:09:19Z</updated>
<published>1976-05-04T00:00:00Z</published>
<summary type="text">Evaluation of wire fences for control of coyote depredations
Thompson, Bruce Carlyle
See pdf
Graduation date: 1976
</summary>
<dc:date>1976-05-04T00:00:00Z</dc:date>
</entry>
</feed>
