Student Research in the Biology Department

The PC biology faculty is quick to point out that a good education is not limited to the classroom.
There are educational research projects and journeys available.

Click on the links/pictures below to view a PDF presentation about recent student researches.
(You'll need Adobe Acrobat Reader™ to view the documents)
  1. Development and Function in the Mammalian Placenta and Umbilicus: Robyn Fredrick & Katie Kelly (view PDF)
  2. Embryogenesis in the Japanese Medaka, Oryzias latipedes (view PDF)
  3. Embryogenesis in the sea urchin, Arbacia: In Vitro fertilization and ‘Induced Twinning’ (view PDF)
  4. Pituitary Adenlyate Cyclase Activiting Polypeptide is a Potent Chloride Secretagogue in the Shark, Squalus acanthias, Rectal Gland (view PDF)
    J. Stidham: Presbyterian College & Mount Desert Island Biological Laboratory
  5. A Comparative Study of Snake Scale Microdermatoglyphics. Ryan Williamson & Dr. Michael Rischbieter (view PDF)

Summer Research 2004 (Laurel Hickman & Erica Raheja) - Freshwater Mussel Ecotoxicology


Laurel Hickman, Bob Hudson and Erica Raheja (left to right) examine a mussel parent for mature larvae (glochidia)


Laurel Hickman (foreground) and Erica Raheja (background) collecting parent mussels in Parson's Mountain Lake
July 28, 2004. The Presbyterian College Biology Department was awarded another contract from The Tennessee Wildlife Resources Agency which allows one PC student, Laurel Hickman, to work as a summer intern with Dr. Bob Hudson, conducting research in freshwater mussel ecotoxicology. This research involves toxicological testing using freshwater mussel juveniles which are artificially cultured in the laboratory. This research ultimately leads to cleaner water, helping governing officials set proper safe levels for many river effluents. Furthermore, Dr. Ron Zimmerman and Dr. Hudson had one Governor's School Student (Erica Raheja) who worked on a six-week internship investigating the effect of immunization on success of mussel larval attachment on fish. Finally, Erica attempted inoculation of mussel larvae on different species of fish in an attempt to determine which species have the highest transformation success.


Honors Project (Laurel L. Delaney & Mary Douglass Hayne) - A Floral Analysis of the Pleistocene Camelot Fauna

Click here to view Laurel's and Mary Douglass's research proposal (Word document)

November 30, 2003.
The Pleistocene spanned from 1.8 million to 11,000 years ago and was characterized by drastic environmental changes and the expansion of the polar icecaps. Animal remains such as the Glyptodont, Mammoth, and Giant Beaver have been found and examined from a site near Harleyville, SC called “Camelot.” However, the floral remains have not yet been studied. Layers of carbonized plant remains have been found, including pollen, seeds, leaves, twigs and nuts. The first part of the study will use dissecting and light microscopes to study the stems, leaves, and reproductive portions of the plants found at the site. The second part of the study will examine the pollen using the scanning electron microscope, comparing it to contemporary pollen.



Honors Project (Matt Madden) - Analysis of the GPR50 Gene’s Involvement in X-Linked Mental Retardation in Chromosomal Region Xq28

Click here to view Matt's research proposal (Word document)

February 2, 2003.
Analysis of the GPR50 Gene’s Involvement in X-Linked Mental Retardation in Chromosomal Region Xq28. X-linkage in mental retardation (MR) was first suspected during the 1970s with the identification of fragile X and predictions now estimate that as many as 200 X-Linked MR genes may exist The purpose of this research then is to explore GPR50, a gene located in chromosomal region Xq28, for its possible involvement in X-Linked Mental Retardation (XLMR). GPR50, which consists of only two coding exons, encodes for H9, a novel member of the G protein-coupled melatonin receptor family thought to be involved in neurological signal transduction. An attempt to locate mutations within the GPR50 gene was then made using a pool of approximately 550 males with mental retardation of unknown etiology. In exon 1, a nested PCR was first performed to amplify the region followed by amplicon sequencing using a MegaBACE sequencer. Exon 2 still awaits investigation. To date, around 300 of the 550 male genetic samples have been examined for variations within exon 1. Variations indicating the possibility of a mutation have been found in 9 of the 300 individuals including suspected base pair substitutions and insertions. These variations now await further confirmation through both restriction endonuclease digest results and more complete MegaBACE sequencing results using both a forward and reverse primer. Clearly, much more analysis is needed to ascertain whether these potential variations point to a role of GPR50 in XLMR.



Honors project (Christina Ball and Beth Bailey) - Isolating fish chromosomes from the Sunfish family, Centrarchidae

January 23, 2003. Senior Biology Majors Christina Ball and Beth Bailey are isolating fish chromosomes from the Sunfish family, Centrarchidae, in order to compare the different banding patterns in an effort to compare the evolution of the different genera. Kidney cells will be cultured and slides will be viewed using a technique called q banding with fluorescent microscopy to identify banding patterns of the chromosomes. Although these fish have had their phylogeny described by hybridization experiments as well as morphological characteristics, chromosome rearrangements and their role in
the evolution of this group has never been elucidated.



Honors project (Dawn Oxner & Amanda Brinson) - Isolation and Characterization of Antibiotics from Chitin Amended Soils

For an updated desciption of the research project, click here (Word document, 19.0KB).

January 16, 2003.
Using a soil enrichment technique to enhance the growth and recovery of Actinomycetes in soils, we will seek to uncover novel antibiotics from this unique group of bacteria. Following isolation of antibiotic producing strains we will characterize and attempt to identify the biologically active compounds.
 -- Dawn Oxner & Amanda Brinson --