Contribution of Freshwater Bivalves to Muskrat Diets in the Green River, Mammoth Cave National Park, Kentucky

Muskrats (Ondatra zibethicus) are known to prey on freshwater bivalves (mussels and clams) and can negatively impact imperiled mussel species. However, factors that infl uence muskrat predation on bivalves are poorly understood. We evaluated the feeding ecology of muskrats at Mammoth Cave National Park, Kentucky by using stable isotope analysis of muskrat hair samples and by monitoring bivalve shell deposition at muskrat middens. Bayesian mixing-model analysis of stable isotope δ15N and δ13C ratios revealed that the median muskrat biomass derived from bivalves was 51.4% (5th and 95th percentiles were 39.1 to 63.4%, respectively), a much higher dietary proportion than previously reported. Shell depositions by muskrats at middens decreased with the availability of seasonal emergent vegetation, suggesting that the consumption of animal matter is in response to a scarcity of plant foods. Our results add to the growing body of evidence that muskrats have the potential to impact mussel population growth and recovery in some environments

Superconducting phases of f-electron compounds

Intermetallic compounds containing f-electron elements display a wealth of superconducting phases, that are prime candidates for unconventional pairing with complex order parameter symmetries. For instance, superconductivity has been found at the border of magnetic order as well as deep within ferro- and antiferromagnetically ordered states, suggesting that magnetism may promote rather than destroy superconductivity. Superconductivity near valence transitions, or in the vicinity of magneto-polar order are candidates for new superconductive pairing interactions such as fluctuations of the conduction electron density or the crystal electric field, respectively. The experimental status of the study of the superconducting phases of f-electron compounds is reviewed.Comment: Rev. Mod. Phys. in print; 75 pages, 23 figures; comments welcom

Phenotypic Screen of Early-Developing Larvae of the Blood Fluke, Schistosoma mansoni, using RNA Interference

RNA interference (RNAi) represents the only method currently available for manipulating gene-specific expression in Schistosoma spp., although application of this technology as a functional genomic profiling tool has yet to be explored. In the present study 32 genes, including antioxidants, transcription factors, cell signaling molecules and metabolic enzymes, were selected to determine if gene knockdown by RNAi was associated with morphologically definable phenotypic changes in early intramolluscan larval development. Transcript selection was based on their high expression in in vitro cultured S. mansoni primary sporocysts and/or their potential involvement in developmental processes. Miracidia were allowed to transform to sporocysts in the presence of synthesized double-stranded RNAs (dsRNAs) and cultivated for 7 days, during which time developing larvae were closely observed for phenotypic changes including failure/delay in transformation, loss of motility, altered growth and death. Of the phenotypes evaluated, only one was consistently detected; namely a reduction in sporocyst size based on length measurements. The size-reducing phenotype was observed in 11 of the 33 (33%) dsRNA treatment groups, and of these 11 phenotype-associated genes (superoxide dismutase, Smad1, RHO2, Smad2, Cav2A, ring box, GST26, calcineurin B, Smad4, lactate dehydrogenase and EF1α), only 6 demonstrated a significant and consistent knockdown of specific transcript expression. Unexpectedly one phenotype-linked gene, superoxide dismutase (SOD), was highly induced (∼1600-fold) upon dsRNA exposure. Variation in dsRNA-mediated silencing effects also was evident in the group of sporocysts that lacked any definable phenotype. Out of 22 nonphenotype-expressing dsRNA treatments (myosin, PKCB, HEXBP, calcium channel, Sma2, RHO1, PKC receptor, DHHC, PepcK, calreticulin, calpain, Smeg, 14.3.3, K5, SPO1, SmZF1, fibrillarin, GST28, GPx, TPx1, TPx2 and TPx2/TPx1), 12 were assessed for the transcript levels. Of those, 6 genes exhibited consistent reductions in steady-state transcript levels, while expression level for the rest remained unchanged. Results demonstrate that the efficacy of dsRNA-treatment in producing consistent phenotypic changes and/or altered gene expression levels in S. mansoni sporocysts is highly dependent on the selected gene (or the specific dsRNA sequence used) and the timing of evaluation after treatment. Although RNAi holds great promise as a functional genomics tool for larval schistosomes, our finding of potential off-target or nonspecific effects of some dsRNA treatments and variable efficiencies in specific gene knockdown indicate a critical need for gene-specific testing and optimization as an essential part of experimental design, execution and data interpretation