Examples of Undergraduate
Research Projects
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Advisor(s) |
Dr.
Janice Glime
Professor,
Biological Sciences
Dr.
Andrew Storer
Assistant
Professor, Forestry |
| Student Researcher |
Janet Frederick |
| Project Title |
Lure
Effectiveness at Attracting Wood Boring Insects in Different Forest Types |
| Sponsor |
School of Forest Resources and Environmental Science
and NSF REU Program |
| Abstract |
There
are many different chemicals used to attract wood boring insects.
A new lure has recently been developed to attract long-horned beetles
(Coleoptera: Cerambycidae) but the chemical composition is not available
as it is proprietary information. Several experiments were conducted
to determine the effectiveness of this new lure compared with some
commonly used lures, such as those releasing high doses of ethanol
and alpha-pinene. These experiments were conducted in two forest
types to determine the new lures attractiveness to bark and wood
inhabiting insects in deciduous and coniferous forests. The new
lure caught significantly more long-horned beetles in coniferous
forests compared with other lures, though trap catches were small.
It was found that Cleridae and Scolytidae were attracted to the
new long-horned beetle lures in large numbers. |
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Advisor(s) |
Dr.
Casey Huckins
Associate
Professor, Biological Sciences |
| Student Researcher |
Liang Yin |
| Project Title |
Studies
on fish scale formation and development in brook trout (Salvelinus
fortinalis) |
| Sponsor |
Phi
Sigma National Biology Honor Society |
| Abstract |
The
ability to accurately determine fish age and growth is a critical
tool in the continued study of fish ecology. There are several approaches:
capture-mark-recapture, length-frequency distributions, back-calculation
using previous data, and hard part examination (Jearld 1983). Within
these, fish scale analysis is an economical and easy way to estimate
fish age and growth (Szedlmayer 1991). In my experiment, I undertake
investigations on juvenile brook trout using alizarin red staining
and light microscopy. My goal is to know whether there is relationship
between the formation of fish scales and fish age, the formation
of fish scales and fish length, and what the relationship is. Over
the course of the research, I am more convinced that scale formation
is more closely related to fish length than to fish age. |
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Advisor(s) |
Dr.
Donald R. Lueking
Associate
Professor, Dir. of Graduate Studies, Biological Sciences |
|
Student Researcher |
James Y. Wee |
| Project Title |
Comparison
of the Membrane Protein Profiles of Glucose and Naphthalene Grown
Cells of Pseudomonas fluorescens strain Uper-1 |
| Sponsor |
MTU
Department of Biological Sciences |
| Abstract |
Naphthalene
is a polycyclic aromatic hydrocarbon (PAH) and is known to be both
mutagenic and carcinogenic. Although numerous studies have appeared
concerning the mechanism of naphthalene catabolism by microorganisms,
the mode of assimilation of naphthalene, and other PAH’s, by microorganisms
remains unclear. Since the bioremediation of PAH’s in soil and
water relies upon the presence of an efficient acquisition system,
as well as an efficient mechanism for catabolism, our studies have
focused upon the mode of assimilation of PAH’s by members of the
genus Pseudomonas. Previous studies (Whitman et al., 1995) have
indicated that P. fluorescens strain Uper-1 possesses an active
transport system for the assimilation of naphthalene. However, such
a transport system has never been identified. Our studies, therefore,
are focused upon comparing the membrane protein profiles of glucose
grown and naphthalene grown cells of P. fluorescens strain Uper-1
in an initial attempt to identify membrane-associated proteins specifically
expressed in naphthalene grown cells. It is proposed that one,
or more, of these proteins may be involved in the active assimilation
of naphthalene. Strain Uper-1 was grown on media with either glucose
or naphthalene as the sole source of carbon and the cells were harvested
by centrifugation, disrupted and a crude membrane preparation was
obtained by differential centrifugation. This membrane was then
layered onto a sucrose gradient and subjected to an 18 h centrifugation
to resolve the cytoplasmic and outer membranes. Gradients were hand-fractionated
and the positions of the outer and inner membranes were determined
by the measurement of NADH oxidase activity, KDO (2-keto-3-deoxy-D-manno-octonic
acid) and total protein distribution of the fractions. Fractions
containing the outer and inner membranes were then individually
collected and concentrated by centrifugation and the protein profiles
of these fractions were evaluated by SDS-PAGE. Proteins present
in the membranes from naphthalene grown cells, but absent from the
membranes of glucose grown cells, were identified as proteins putatively
involved in naphthalene assimilation. These proteins are currently
being sequenced and this information will be utilized to identify
and isolate the genes that encode the information for their production.
The ultimate objective of this research is to further the understanding
of PAH assimilation and catabolism of PAH’s and to use this information
for the improvement of procedures for engineered PAH bioremediation. |
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