The parasitic nematodes Ancylostoma caninum and Oesophagostomum radiatum were collected and analyzed for intestinal inorganic granules. Three means of identification were utilized to determine the composition granules, including birefringence, x-ray diffraction and energy dispersive spectrometric (EDS) analysis. Initial x-ray diffraction results of the two worms showed a calcium sulfide presence within the worms. Closer examination of the granules within Ancylostoma caninum however, utilizing EDS analysis revealed their composition to be zinc sulfide. These results concur with those of Rogers (1940) and Clark (1956) who found zinc sulfide granules in several species of Strongylus. The ZnS granules seem to be a result of a detoxification function that binds excess zinc and sulfhydryl groups present from the ingestion and breakdown of dietary blood meals.

Morphological variation between geographically distant populations has long been recognized. The primary objective of this study was to test whether nonrandom shifts in morphology have occurred across a 150-year time span in two rare, endangered plant species Geum radiatum and Houstonia montana. During the last century the vegetation on Roan Mountain has undergone numerous environmental pressures that may have produced morphological shifts. A diverse suite of morphological characters was measured from both species. Characters included vegetative and reproductive structures. Herbarium specimens and direct field measurements were the sources of material used. Results indicated a significant increase in size across time in the majority of characters measured. Results of this study challenge standard taxonomic practices, present questions pertaining to the relationship between genetics and morphology, and raise issues concerning conservation and management strategies of endangered plant populations.

The ventral tegmental area (VTA) is an important component of the mesolimbic dopamine circuit and processes reward and motivational behaviors. In response to drug exposure, synaptic connections of this circuit can be rewired via synaptic plasticity—a phenomenon thought be responsible for the pathology of addiction. While much is known about dopamine neuron plasticity, less is known regarding plasticity exhibited by VTA GABA cells, specifically inhibitory inputs from outside the VTA. Expanding on the work of Bocklisch et al. (2013), we investigated the plasticity of inhibitory inputs to VTA GABA neurons. Using whole cell electrophysiology in GAD67 GFP mice, we observed that these VTA GABA cells can experience either long-term potentiation (LTP) or long-term depression (LTD) in response to a 5 Hz stimulus. While neither the LTP nor LTD appear to be mediated by the cannabinoid-1 receptor (CB1), the nitric oxide synthase (NOS) pathway, or the dopamine-2 (D2) receptor, the LTP is blocked by APV, an NMDA receptor antagonist, and the LTD is blocked by CGP 54626, an antagonist of the GABAB receptor. Additionally, µ-opioid and adenosine-1 receptors modulated plasticity at this synapse, but chronic morphine administration (10mg/kg) did not block the observed LTP or LTD. Furthermore, we used an optogenetic approach in VGAT-Cre mice to target inhibitory inputs from the lateral hypothalamus (LH) to the VTA. An optical stimulus (5 Hz) caused these inputs to depress, which has not been previously described and may be behaviorally important in reward processing. These novel findings increase our understanding of VTA neural circuitry, ultimately increasing our capacity to better comprehend and treat the pathology of addiction. Additionally, changes in synaptic strength in hippocampal CA1 pyramidal cells are thought to be responsible for the acquisition and retention of short-term memory. Feedforward stratum radiatum interneurons of many subtypes experience LTD, short-term depression (STD), or lack of plasticity, but it is not known whether plasticity correlates with specific interneuron subtypes. Using whole cell electrophysiology and qPCR, we characterized the plasticity expressed by hippocampal interneurons in correlation with their mRNA expression patterns to determine cell subtype. We also assessed the expression of endocannabinoid (eCB) biosynthetic enzymes as well as metabotropic glutamate receptor subunits known to mediate plasticity. Cells exhibiting LTD tended to express mRNA for at least one of the eCB biosynthetic enzymes and the metabotropic glutamate receptor subunit mGluR5. mGluR5 was not expressed by cells exhibiting STD or no plasticity. Cells that exhibited short-term depression tended to express mRNA for at least one of the eCB biosynthetic enzymes, but not mGluR5. This suggests that stratum radiatum interneuron plasticity can be predicted based on mGluR expression, and that these different types of plasticity may have some importance in hippocampal function.