997 research outputs found

    Revenge of the host: cannibalism, ontogenetic niche shifts, and the evolution of life-history strategies in host-parasitoid systems

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    Question: How does cannibalism in the host alter the evolution of a parasitoid’s oviposition strategy? Can differences in cannibalism risk between parasitized and healthy hosts alter the stage-specific foraging of parasitoids? Can host-specific differences in cannibalistic behaviour explain why parasitoids vary in what host stages they attack? Mathematical methods: We examined the evolutionary dynamics of a stage-structured host–parasitoid model using two complementary approaches: (1) individual-based numerical simulations of evolutionary dynamics, and (2) the theory of adaptive dynamics focusing on evolutionarily stable strategies (ESSs). Assumptions: Cannibalism in the host is assumed to be stage structured, with larger stages consuming smaller stages. The consumption of parasitized hosts also results in killing of the parasitoid’s offspring. Vulnerability to cannibalism of parasitized versus healthy hosts was allowed to vary. The parasitoid’s preference for attacking early versus late host stages was the trait under selection and allowed to evolve. Results: When cannibalism rates increase relative to the parasitoid’s attack rates, the ESS of the parasitoid shifts from attacking only early host stages to attacking only late host stages. This shift occurs at lower cannibalism rates when parasitized hosts are more susceptible to cannibalism than healthy hosts. Under equilibrium conditions, a small boundary area exists between these two regions where attacking only early or only late host stages are alternative ESSs. The threshold and alternative stable ESSs are the result of cannibalism, which creates a positive feedback between the parasitoid’s oviposition rate and its own mortality. Intermediate strategies, where parasitoids evolve to attack both stages, occur only when host populations exhibit large population oscillations or when generalist parasitoids that attack both stages have a foraging advantag

    On-orbit Metrology and Calibration Requirements for Space Station Activities Definition Study

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    The Space Station is the focal point for the commercial development of space. The long term routine operation of the Space Station and the conduct of future commercial activities suggests the need for in-space metrology capabilities analogous when possible to those on-Earth. The ability to perform periodic calibrations and measurements with proper traceability is imperative for the routine operation of the Space Station. An initial review, however, indicated a paucity of data related to metrology and calibration requirements for in-space operations. This condition probably exists because of the highly developmental aspect of space activities to date, their short duration, and nonroutine nature. The on-orbit metrology and calibration needs of the Space Station were examined and assessed. In order to achieve this goal, the following tasks were performed: an up-to-date literature review; identification of on-orbit calibration techniques; identification of sensor calibration requirements; identification of calibration equipment requirements; definition of traceability requirements; preparation of technology development plans; and preparation of the final report. Significant information and major highlights pertaining to each task is presented. In addition, some general (generic) conclusions/observations and recommendations that are pertinent to the overall in-space metrology and calibration activities are presented

    Renal peroxiredoxin 6 interacts with anion exchanger 1 and plays a novel role in pH homeostasis.

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    Peroxiredoxin 6 (PRDX6) is one of the six members of the PRDX family, which have peroxidase and antioxidant activity. PRDX6 is unique, containing only one conserved cysteine residue (C47) rather than the two found in other PRDXs. A yeast two-hybrid screen found PRDX6 to be a potential binding partner of the C-terminal tail of anion exchanger 1 (AE1), a Cl(-)/HCO(3)(-) exchanger basolaterally expressed in renal α-intercalated cells. PRDX6 immunostaining in human kidney was both cytoplasmic and peripheral and colocalized with AE1. Analysis of native protein showed that it was largely monomeric, whereas expressed tagged protein was more dimeric. Two methionine oxidation sites were identified. In vitro and ex vivo pull-downs and immunoprecipitation assays confirmed interaction with AE1, but mutation of the conserved cysteine resulted in loss of interaction. Prdx6 knockout mice had a baseline acidosis with a major respiratory component and greater AE1 expression than wild-type animals. After an oral acid challenge, PRDX6 expression increased in wild-type mice, with preservation of AE1. However, AE1 expression was significantly decreased in knockout animals. Kidneys from acidified mice showed widespread proximal tubular vacuolation in wild-type but not knockout animals. Knockdown of PRDX6 by siRNA in mammalian cells reduced both total and cell membrane AE1 levels. Thus, PRDX6-AE1 interaction contributes to the maintenance of AE1 during cellular stress such as during metabolic acidosis.Human kidney sections were prepared by Suzy Haward, Addenbrooke's Human Research Tissue Bank, which is supported by the Cambridge Biomedical Research Centre. We thank Dr. Aron Fisher (Institute for Environmental Science, University of Pennsylvania) for the kind gift of Prdx6−/− mice and reagents, Carsten Wagner (Zurich) for antisera, Jane Clarke (University of Cambridge) for modified pRSET-A vector, and Kamburapola Jayawardena for mass spectrometry (CIMR). This work was funded by the Wellcome Trust (award 088489/Z/09/Z to FEKF and Strategic award 100140/Z/12/Z to the Cambridge Institute for Medical Research), and the Jack Kent Cooke Foundation (scholarship to SLS).This is the author accepted manuscript. The final version is available from Nature Publishing Group via http://dx.doi.org/10.1038/ki.2015.27

    Relaxation rate of the reverse biased asymmetric exclusion process

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    We compute the exact relaxation rate of the partially asymmetric exclusion process with open boundaries, with boundary rates opposing the preferred direction of flow in the bulk. This reverse bias introduces a length scale in the system, at which we find a crossover between exponential and algebraic relaxation on the coexistence line. Our results follow from a careful analysis of the Bethe ansatz root structure.Comment: 22 pages, 12 figure

    Biomethane Yield from Different European Phragmites australis Genotypes, Compared with Other Herbaceous Wetland Species Grown at Different Fertilization Regimes

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    Phragmites australis, Typha latifolia, T. angustifolia and Arundo donax are tall wetland graminoids with the potential to replace fossil fuels under sustainable cultivation conditions. We investigated the biomethane (CH4) production of these four species, including four different genotypes of P. australis, which represent the high intraspecific diversity of European reed. All plants were grown under three different macronutrient supplies (no nutrients added, an equivalent of 75 kg N ha−1 year−1 added and an equivalent of 500 kg N ha−1 year−1 added). Biomethane production was measured in four independent batch digestion tests. Across all experiments, fertilization regime had little effect on CH4 yield, which was on average 222 ± 31 L kg−1 volatile solids (VS). The lowest yield was produced by T. angustifolia (140 L kgVS−1) receiving no nutrients, while the highest yield was produced by A. donax (305 L kgVS−1) in the highest nutrient treatment. The intraspecific diversity of P. australis did not affect biomethane production. All P. australis genotypes produced on average 226 ± 19 L CH4 kgVS−1, which, although high, was still lower than conventional biogas species. The biomass production of P. australis was less increased by fertilization than that of Typha sp. and A. donax, but all species had similar biomass without fertilization

    Renal Foreign Bodies

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/67109/2/10.1177_000992286900800511.pd
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