Biology students interested in summer research at Williams--

 

To learn about honors research opportunities, use the following resources:

 

á      Information session with faculty Tuesday February 12 at 7:00 PM in TBL 112

 

 

á      Department website: http://www.williams.edu/Biology/Research/Summer/summer.shtml

 

Application deadline is February 18th

 

 

 

 

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Faculty accepting summer students for Summer 2008

 

Art, Banta, Edwards, Hutson, Lynch, Morales, and Ting

 

[descriptions of their research are below; print copies of this info will be available at the Tuesday info session and outside the Biology Department Office TBL 219]

 

 


Hank Art

TBL 302 (Laboratory), TBL 203 (Office), x2461, hart@williams.edu

 

 

Vernal Pool Ecology

Adjacent to the Hopkins Memorial Forest are two vernal pools  (predator-free shallow pools that are prone to drying-out during the summer) known to provide breeding habitat for spotted salamanders, spring peepers, wood frogs, and the rare JeffersonÕs salamander.  Other species of amphibians and reptiles use these pools as well.  This project involves the monitoring of drift fences and pitfall traps to determine the phenology, directions of migrations, sex distributions, population structures, etc. of amphibians utilizing these pools during their breeding seasons (starts in mid-March to early April and continues for various species through the  summer). The data for 2007 will be compared with that collected in 2006 to determine the degree of fidelity in migration patterns for spotted salamanders.     Digital videos of the peak of the salamander and wood frog mating season can be seen at:  http://www.williams.edu/CES/hopkins/landscape/video.htm

 

 

Birch Strips & Woodlots: The Impacts of Land Use on Forest Recovery

In the Hopkins Forest there are two on-going observational experiments that investigate the recovery of biotic communities following massive disturbances.  One of these sites is the ÒFarm Forestry Unit,Ó a tract that was a 18th Century woodlot that appears to have been clear-cut around the mid-19th Century and now supports a magnificent red oak stand.  This tract has been periodically censused since 1947, the last time in 2001.  The other site is the ÒBirch Strips,Ó a field experiment initiated by the U.S. Forest Service in 1954 and periodically inventoried, most recently in 1996.  The Birch Strips were clear cut and soils treated differentially in an attempt to regenerate paper birch.  The reinventory and interpretation of these two sites will give insights into how human disturbances of primary and secondary woodlots influence community composition, biomass accumulation, and carbon processing in Northeastern forests.  The changes in these manipulated stands will be compared to the changes evident in the old aged Beinecke Stand, which will also be reinventoried.


Lois Banta

TBL301 (Laboratory), TBL213 (Office), x4330, lbanta@williams.edu

 

In the Banta lab, we study the interactions between the soil bacterium Agrobacterium tumefaciens and its host plants.  In particular, we are interested in the transport of a large fragment of DNA across the membrane system surrounding the bacterium, and in the plant defense responses elicited by the bacterium.  Infection of susceptible plants by A. tumefaciens results in crown gall tumor formation.  The disease mechanism involves the transfer and integration into the plant genome of a specific DNA molecule (T-DNA) from a bacterial tumor-inducing (Ti) plasmid).  Sequences on the T-DNA encode enzymes responsible for the biosynthesis of plant growth hormones; expression of these genes in the host plant leads to uncontrolled hormone production and hence unregulated plant cell division ("plant cancerÓ).  This naturally occurring process of DNA transfer to plants is widely used to introduce new genes into plants, but its utility is limited by the fact that some plants, including the agriculturally important grains rice, wheat, corn and barley, are poor hosts.  Thus, advances in our understanding of the mechanism of DNA delivery, and in particular the contributions made by bacterial proteins that are required for infection of some but not all hosts, may further the work of those scientists engaged in efforts to increase global food productivity.

T-DNA processing and transfer are mediated by a number of Ti plasmid-encoded virulence (Vir) proteins.  Movement of the T-DNA requires the eleven products of the virB operon, as well as the VirD4 protein.  The goal of our research is to probe the interactions between the VirB/VirD4 pore and the transported substrates, which include not only the T-DNA, but also at least five proteins. The substantial sequence homologies between VirB proteins and the proteins required for pertussis toxin export (causing whooping cough), as well as for pathogenicity in Helicobacter pylori (which causes stomach ulcers and can lead to stomach cancer) and several other bacteria, indicate that our findings regarding assembly of the VirB pore may have important implications for the assembly and functioning of multi-protein transporters responsible for the delivery of a variety of pathogenic substrates to mammalian host cells.

A major goal of my current research is to elucidate the functions of two virulence proteins, VirC1 and VirC2, which appear to enhance the efficiency of T-DNA delivery to the host plant. We postulate that VirC1 and VirC2 work together to tether the Ti plasmid, through VirC1Õs reported affinity for a sequence adjacent to the T-DNA, to the bacterial cell membrane.  Such intimate association between the VirB/D4 transport apparatus and the Ti plasmid would ensure that, in the presence of an attached plant cell, the T-DNA could transit directly into the recipient cell.  Maggie Lowenstein Õ07 and Oliver BurtonÕ06, together with lab technician Gape Machao Ô06 have been using biochemical and molecular approaches to confirm the key tenets of this hypothesis. The observation that the virC operon is required for virulence on some, but not all, host species has led us to hypothesize further that efficient delivery of T-DNA may be essential in overcoming the host defenses normally mounted by plants in response to Agrobacterium infection.  Merritt Edlind Õ07 is currently exploring the defense responses in the model plant Arabidopsis and their role in determining the efficiency of the infection process.  The ability of VirC1 and VirC2 to modulate host cell responses will be a possible subject of research for next yearÕs students.  Finally, Ian Buchanan Õ07 has been using fluorescence and scanning electron microscopy to study the attachment of Agrobacteria to the host plant.  The extracellular polysaccharides (EPS) that surround the bacteria appear to play a key role in attachment to the plant, and may also influence whether the bacterium is perceived by the plant as a threat.  We have initiated a genomics project to investigate the assembly of this EPS and its contribution to host range, and future students will be able to pursue this topic.

 

Joan Edwards

TBL012 (Laboratory); TBL217 (Office); x2472; jedwards@williams.edu

 

My research covers three broad areas: the mechanisms and adaptive behavior of ultra-rapid movements in plants, the adaptive significance of transparency in the larvae of  and insects and long-term plant population dynamics.

 

Studies of the adaptive behavior of ultra-rapid movements in plants focus on how plants carry out rapid movements and why they behave this way. Much of this work is done collaboratively with Prof. Dwight Whitaker in the Physics Department.  Examples of study plants include a.) bunchberry (Cornus canadensis), which we have discovered has the fastest blooming flower (opens in <0.05ms!), b.) sphagnum moss (Sphagnum spp.) which has a spore-filled capsule that explodes open propelling the spores over 15cm into the air, c) fruit explosion in touch-me-not (Impatiens spp.), which use a slingshot-lime mechanism to propel seeds away from the parent plant, d.) catapulting pollen in gaywings (Polygala paucifolia), and stinging nettle (Urtica spp.).  These studies involved using high-speed cameras (filming at up to 30,000fps), microscopy (including SEM and EM), and work in the field that focuses on understanding the plants in situ.

 

The studies of the behavior of the sawfly, Empria obscurata, focus on determining their life history characteristics and the adaptive significance of having larvae that are transparent.  These remarkable larvae turn the color of whatever they eat so that they can remain cryptically colored even when eating very different colored foods. So far, our studies have shown that larvae that eat both flowers (yellow) and leaves (green) have higher survivorship, achieve a larger adult size and develop more quickly that larve fed on either flowers or leaves alone.  The sawfly work will continue with life history studies but also explore potential for speciation in Empria by host-shift.

 

The long-term plant population studies currently focus on two species: a.) the population growth and impact of the invasive plant, Alliaria petiolata (Garlic mustard) and the growth, survivorship and reproduction of arctic plants which are growing at the southern edge of their range on Isle Royale National Park, Lake Superior.  For the Garlic Mustard study we just completed the 8th year of observation of three sub-populations in early, mid- and late successional sites.  We also are maintaining removal plots where we are measuring the impact of garlic mustard on native plant populations.  For the arctic plant study we have permanently marked individuals of arctic and non-arctic plants which we have followed since 1998.   The artic plants are at the southernmost edge of their ranges and are sub-populations that are most likely to be impacted by global warming. We are measuring the changes in these populations in response to changes in climate. 

 

 A summary of the projects include working on:  


Lara Hutson

BSC 032 (Laboratory); TBL201 (Office); x4508, lhutson@williams.edu

 

Our laboratory is interested how members of the small heat shock protein family regulate embryonic development in the zebrafish (Danio rerio). Our primary focus is on how HSP27 regulates the migration of neuronal growth cones, and thus overall wiring of the nervous system, by virtue of its ability to regulate actin cytoskeletal dynamics. In addition, we are currently beginning to test development of skeletal and smooth muscle development. Ultimately, we plan to identify all sHSPs in the zebrafish (there are predicted to be at least ten) and systematically analyze the function of each during normal development and in protection from environmental stressors. The primary techniques we use to explore these questions include molecular cloning (to identify sHSP cDNAs), in situ hybridization (to examine mRNA expression patterns), dye labeling (to fluorescently label growth cones in fixed and living zebrafish embryos), immunohistochemistry (to analyze the consequences of gene disruption), generation and analysis of transgenic zebrafish (to misexpress sHSP gene variants in our tissue of choice), and confocal microscopy (to image growth cones in intact embryos). For more information, and links to timelapse movies of growth cones, please visit

https://www.williams.edu/Biology/Faculty_Staff/lhutson/lhutson.shtml.

 

 

Daniel Lynch

BSC 261 (Laboratory), BSC262 (Office), x2330, dlynch@williams.edu

 

Sphingolipids have been demonstrated to play important roles as both membrane components and as signaling molecules involved in regulating cellular processes in animals and fungi.  While sphingolipids are quantitatively important components of specific plant membranes and recent evidence points to sphingolipids serving as signaling molecules in plants, surprisingly little is known about plant sphingolipid function.  Research in the Lynch lab, funded by the NSF 2010 program (to characterize all 26,000 genes in Arabidopsis thaliana) is focusing on the network of genes predicted to be involved in plant sphingolipid metabolism.  These genes will be identified and the functions of the respective protein products of the genes (e.g., the specific reaction catalyzed by the gene product, its substrate specificity, subcellular location, expression and activity in tissues) will be determined. As opportunities arise, the specific roles of different sphingolipids in plants will be investigated by characterizing the properties and behavior of mutant plants defective in specific sphingolipid metabolic genes and so incapable of synthesizing a given sphingolipid.  These various projects will involve aspects of molecular biology and biochemistry (including lipid analysis and assays of enzyme activities) in addition to others.

 

 

Manuel Morales

TBL 011 (Laboratory); TBL215 (Office); x2983, mmorales@williams.edu

 

Research in my lab focuses on understanding the population dynamics of insect-plant interactions, especially mutualism. Summer research projects and theses are typically field based. Currently, my research explores aspects of the mutualism between ants and treehoppers, an insect that feed on goldenrod plants. In this interaction, ants collect the sugar-rich excretions ("honeydew") of treehoppers in return for protecting treehoppers from predators and pathogens.

 

The main research projects this summer will be a study exploring the role of mutualism with treehoppers on the spread of an invasive ant recently discovered in Williamstown, and the analysis of vibrational communication between ants and treehoppers. This research will take place at Hopkins Memorial Forest as well as field sites bordering the Hoosic River throughout NY, VT, and MA.

 

More detailed information on my research (including study system) can be

accessed from my web site (http://mutualism.williams.edu)

 



 Claire Ting

TBL 023 (Laboratory); TBL 214 (Office), x4053, cting@williams.edu

 

Photosynthesis is a fundamental biological process upon which the majority of Earth's life depends. Research in my laboratory focuses on photosynthetic processes and proteins and on the response of photosynthetic organisms to environmental stress. Projects are interdisciplinary in nature and integrate tools and concepts from fields including biochemistry, cell biology, genomics, ecology, and evolution.

 

Text Box: A.      B.  

Electron microscopy is a technique that is used routinely in my laboratory for visualizing the ultrastructure of photosynthetic organisms. Scanning electron microscopy (A), traditional transmission electron microscopy (B), and cryo-electron tomography can reveal important changes in cellular architecture following the exposure of organisms to environmental stress. 
One area we are addressing is how differences at the genome level between closely related photosynthetic organisms translate into selective physiological advantages in photosynthetic capacity and in tolerance to abiotic stress. For this project, we are focusing on the environmentally important marine cyanobacteria, Prochlorococcus and Synechococcus. These cyanobacteria are the most abundant photosynthetic prokaryotes in the world's oceans, and in certain regions, more than 10,000 cells can be found in a single drop of sea water. In particular,  Prochlorococcus  plays a key role in marine primary production and in global energy cycles, and because it evolves oxygen and possesses a chlorophyll a/b light-harvesting antenna complex, it is an excellent model for plant photosynthesis. In recognition of their ecological significance, the complete genomes of several Prochlorococcus and Synechococcus strains have been sequenced recently. We have used our comparative genomic analyses and genome-based predictions as the foundation for our laboratory experiments examining photosynthesis and stress response mechanisms. Although Prochlorococcus is closely related to marine Synechococcus, it has evolved striking differences in its photosynthetic apparatus and biological responses to major environmental factors, including temperature and light.