7,826 research outputs found

    Selective Predation by Three Esocids: The Role of Prey Behavior and Morphology

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    We documented differential vulnerability of fathead minnows Pimephales promelas, gizzard shad Dorosoma cepedianum. and bluegills Lepomis macrochirus to predation by muskellunge Esox masquinongy. northern pike E. lucius. and tiger muskellunge E. masquinongy x E. lucius in a 700-L tank. Individual esocids (150-225 mm in total length) were combined with single species groups (N = 15) of optimal-sized prey (25-30% of predator length for bluegills, 37-43% for fathead minnows, and 30-36% for gizzard shad). Capture ability did not differ among esocids; however, mean captures per strike were higher for fathead minnow (0.67) and gizzard shad (0.78) than for bluegill (0.14). Morphology and antipredatory behavior, unique to each prey species, contributed to this differential vulnerability. In the field, we introduced equal numbers and similar sizes of these esocids into two systems, one with centrarchid prey and one with both centrarchid and gizzard shad prey. As predicted from laboratory work, esocids ate fewer prey and grew more slowly when centrarchids were the only prey than they did when gizzard were available. In a third reservoir, containing bluegills and gizzard shad, esocids strongly preferred gizzard shad over bluegills. To maximize growth and survival, esocids should be stocked in systems with soft-rayed or fusiform prey, such as cyprinids or shad, rather than in centrarchid-dominated systems.This study was supported in part by funds from the Federal Aid in Fish Restoration Act under project F-57-R

    Food Consumption and Growth of Three Esocids: Field Tests of a Bioenergetic Model

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    Expression in Escherichia coli of a cloned DNA sequence encoding the pre-S2 region of hepatitis B virus

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    A DNA sequence encoding the entire pre-S2 region (amino acids 120-174; serotype ayw) of human hepatitis B virus envelope protein has been inserted into the lacZ gene of the plasmid pSKS105 yielding a recombinant, pWS3. Lac+ colonies of the Escherichia coli M182 (lacIOPZYA), isolated after transformation with pWS3, produced a pre-S2 peptide-ß-galactosidase fusion protein. This fusion protein, which comprised as much as 3% of the total bacterial protein, was purified to >90% homogeneity by affinity chromatography on p-aminophenyl-ß-D-thiogalactoside-Sepharose. It is immunoprecipitable with rabbit antibodies to a synthetic peptide corresponding to amino acids 120-145 of the pre-S2 region of serotype adw [pre-S(120-145)] or with antibodies to hepatitis B virus. pre-S(120-145) completely blocked the binding of either antibody to the pre-S2 peptide-ß-galactosidase fusion protein. These results indicate that there are antigenic determinants on the fusion protein that are closely related to, if not identical to, determinants on synthetic pre-S(120-145) and on pre-S2 sequences of native hepatitis B virus particles. Thus, bacteria transformed with pWS3 can provide an abundant source of pre-S2-ß-galactosidase fusion protein, which may prove useful either as a diagnostic reagent possessing marker enzyme activity suitable for ELISA tests or as an immunogen with potential to contribute to active prophylaxis of hepatitis B

    Conditional regularity of solutions of the three dimensional Navier-Stokes equations and implications for intermittency

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    Two unusual time-integral conditional regularity results are presented for the three-dimensional Navier-Stokes equations. The ideas are based on L2mL^{2m}-norms of the vorticity, denoted by Ωm(t)\Omega_{m}(t), and particularly on Dm=ΩmαmD_{m} = \Omega_{m}^{\alpha_{m}}, where αm=2m/(4m3)\alpha_{m} = 2m/(4m-3) for m1m\geq 1. The first result, more appropriate for the unforced case, can be stated simply : if there exists an 1m<1\leq m < \infty for which the integral condition is satisfied (Zm=Dm+1/DmZ_{m}=D_{m+1}/D_{m}) 0tln(1+Zmc4,m)dτ0 \int_{0}^{t}\ln (\frac{1 + Z_{m}}{c_{4,m}}) d\tau \geq 0 then no singularity can occur on [0,t][0, t]. The constant c4,m2c_{4,m} \searrow 2 for large mm. Secondly, for the forced case, by imposing a critical \textit{lower} bound on 0tDmdτ\int_{0}^{t}D_{m} d\tau, no singularity can occur in Dm(t)D_{m}(t) for \textit{large} initial data. Movement across this critical lower bound shows how solutions can behave intermittently, in analogy with a relaxation oscillator. Potential singularities that drive 0tDmdτ\int_{0}^{t}D_{m} d\tau over this critical value can be ruled out whereas other types cannot.Comment: A frequency was missing in the definition of D_{m} in (I5) v3. 11 pages, 1 figur
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