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      Physiological proteins in resource-limited herbivores experiencing a population die-off

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          Abstract

          Nutrient availability is predicted to interact with herbivore population densities. Competition for low quality food at high density may reduce summer food intake, and in turn winter survival. Conversely, low population density may favor physiological recovery through better access to better quality spring forage. Here, we take advantage of the long-term study of the Soay sheep population of St. Kilda (Scotland) to measure plasma protein markers and immunity in two consecutive summers with contrasting population densities. We show that, following a winter die-off resulting in a shift to low population density, albumin and total proteins increased, but only in adult sheep. The effect was not solely attributable to selective disappearance of malnourished sheep. Similarly, the concentration of antibodies was higher following the die-off, potentially indicating recovery of immune function. Overall, our results are consistent with the physiological recovery of surviving individuals after a harsh winter.

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          The online version of this article (doi:10.1007/s00114-017-1490-4) contains supplementary material, which is available to authorized users.

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          CLIMATIC VARIABILITY, PLANT PHENOLOGY, AND NORTHERN UNGULATES

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            Fitness correlates of heritable variation in antibody responsiveness in a wild mammal.

            A functional immune system is important for survival in natural environments, where individuals are frequently exposed to parasites. Yet strong immune responses may have fitness costs if they deplete limited energetic resources or cause autoimmune disease. We have found associations between fitness and heritable self-reactive antibody responsiveness in a wild population of Soay sheep. The occurrence of self-reactive antibodies correlated with overall antibody responsiveness and was associated with reduced reproduction in adults of both sexes. However, in females, the presence of self-reactive antibodies was positively associated with adult survival during harsh winters. Our results highlight the complex effects of natural selection on immune responsiveness and suggest that fitness trade-offs may maintain immunoheterogeneity, including genetic variation in autoimmune susceptibility.
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              Risk-sensitive allocation in seasonal dynamics of fat and protein reserves in a long-lived mammal.

              Body reserves of numerous taxa follow seasonal rhythms that are a function of temporal patterns in food availability and life-history events; however, tests of the theory underlying the allocation of somatic reserves for long-lived organisms are rare, especially for free-ranging mammals. We evaluated the hypothesis that allocation of somatic reserves to survival (i.e., metabolic processes) and reproduction should be sensitive to current nutritional state relative to seasonal thresholds in those reserves. Our goal was to reveal the linkages between nutrition and life-history traits to understand how long-lived, iteroparous organisms balance the allocation of somatic reserves to reproduction, while retaining reserves as insurance for survival in unpredictable environments. Our evaluation was based on seasonal dynamics in fat (measured as ingesta-free body fat; IFBFat) and protein reserves (measured as ingesta-free, fat-free body mass; IFFFBMass) of 136 female mule deer (Odocoileus hemionus) over 8 years. Although mean changes in fat and protein reserves were positive over summer and negative over winter, accretion and catabolism of those reserves was not consistent among individuals. Over winter, both lipid and protein stores available in autumn were catabolized in proportion to their availability above a post-winter threshold (5·8% IFBFat, 33 kg IFFFBMass); however, lean body tissue was spared at the expense of lipid reserves. Female deer mostly synthesized lean body tissue over summer and committed post-winter fat reserves to reproduction relative to their availability above an autumn threshold (>8·6% IFBFat), which was lowered by 2·8 percentage points (pp) for each additional young recruited. Mothers reduced their autumn fat threshold to secure current reproductive investment and, thereby, endured a cost of reproduction at the expense of fat accumulation. Allocation of somatic reserves occurred in a risk-sensitive framework; females allocated reserves relative to their availability above seasonal thresholds. In contrast to current notions of summer accretion and winter catabolism of body reserves, some individuals deposited reserves over winter and catabolized reserves over summer, mainly because regulation of individual condition was state-dependent. Consequently, behaviour and life-history strategies may be as much a function of nutritional contributions of the previous season as of the current one. © 2013 The Authors. Journal of Animal Ecology © 2013 British Ecological Society.
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                Author and article information

                Contributors
                +441223337685 , rg535@cam.ac.uk
                Journal
                Naturwissenschaften
                Naturwissenschaften
                Die Naturwissenschaften
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0028-1042
                1432-1904
                31 July 2017
                31 July 2017
                2017
                : 104
                : 7
                : 68
                Affiliations
                [1 ]ISNI 0000 0001 2097 5006, GRID grid.16750.35, Department of Ecology and Evolutionary Biology, , Princeton University, ; Princeton, NJ USA
                [2 ]ISNI 0000000121885934, GRID grid.5335.0, Department of Veterinary Medicine, , University of Cambridge, ; Cambridge, UK
                [3 ]ISNI 0000 0004 1936 738X, GRID grid.213876.9, Odum School of Ecology, , University of Georgia, ; Athens, GA USA
                [4 ]ISNI 0000 0004 1936 7988, GRID grid.4305.2, School of Biological Sciences, , Institute of Evolutionary Biology, University of Edinburgh, ; Edinburgh, UK
                Author notes

                Communicated by: Sven Thatje

                Article
                1490
                10.1007/s00114-017-1490-4
                5537310
                28761976
                16feb5a9-fde0-4fd4-b9a5-844e940d90b3
                © The Author(s) 2017

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 19 February 2017
                : 13 July 2017
                : 15 July 2017
                Funding
                Funded by: Princeton University Health Grand Challenges
                Categories
                Short Communication
                Custom metadata
                © Springer-Verlag GmbH Germany 2017

                Uncategorized
                soay sheep,nutritional ecology,ovis aries,disease ecology
                Uncategorized
                soay sheep, nutritional ecology, ovis aries, disease ecology

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