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      Museum Specimens Bias Measures of Snake Diet: A Case Study Using the Ambush-Foraging Puff Adder (Bitis arietans)

      1 , 1 , 2 , 1
      Herpetologica
      Herpetologists League

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          Fractionation and turnover of stable carbon isotopes in animal tissues: Implications for ?13C analysis of diet

          The use of stable carbon isotopes as a means of studying energy flow is increasing in ecology and paleoecology. However, secondary fractionation and turnover of stable isotopes in animals are poorly understood processes. This study shows that tissues of the gerbil (Meriones unguienlatus) have different δ13C values when equilibrated on corn (C4) or wheat (C3) diets with constant 13C/12C contents. Lipids were depleted 3.0‰ and hair was enriched 1.0‰ relative to the C4 diet. Tissue δ13C values were ranked hair>brain>muscle>liver>fat. After changing the gerbils to a wheat (C3) diet, isotope ratios of the tissues shifted in the direction of the δ13C value of the new diet. The rate at which carbon derived from the corn diet was replaced by carbon derived from the wheat diet was adequately described by a negative exponential decay model for all tissues examined. More metabolically active tissues such as liver and fat had more rapid turnover rates than less metabolically active tissues such as hair. The half-life for carbon ranged from 6.4 days in liver to 47.5 days in hair.The results of this study have important implications for the use of δ13C values as indicators of animal diet. Both fractionation and turnover of stable carbon isotopes in animal tissues may obscure the relative contributions of isotopically distinct dietary components (such as C3 vs. C4, or marine vs. terrestrial) if an animal's diet varies through time. These complications deserve attention in any study using stable isotope ratios of animal tissue as dietary indicators and might be minimized by analysis of several tissues or products covering a range of turnover times.
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            Molecular identification of prey in predator diets.

            In many situations prey choice by predators in the field cannot be established or quantified using direct observation. The remains of some prey may be visually identified in the guts and faeces of predators but not all predators ingest such hard remains and even those that do consume them may also ingest soft-bodies prey that leave no recognizable remnants. The result is, at best, a biased picture of prey choice. A range of molecular techniques and applications are reviewed that allow prey remains to be identified, often to the species and even stage level. These techniques, all of which are still in use, include enzyme electrophoresis, a range of immunological approaches using polyclonal and monoclonal antibodies to detect protein epitopes, and recently developed polymerase chain reaction (PCR)-based methods for detecting prey DNA. Analyses may be postmortem, on invertebrate and vertebrate predators collected from the field, or noninvasive assays of the remains in regurgitated bird pellets or vertebrate faeces. It was concluded that although monoclonal antibodies are currently the most effective method in use today, PCR-based techniques have proved to be highly effective and versatile in recent laboratory trials and are likely to rapidly displace all other approaches.
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              Diet studies of seabirds: a review and recommendations

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                Author and article information

                Journal
                Herpetologica
                Herpetologica
                Herpetologists League
                0018-0831
                1938-5099
                June 2017
                June 2017
                : 73
                : 2
                : 121-128
                Affiliations
                [1 ]School of Animal, Plant and Environmental Sciences, University of the Witwatersrand, Johannesburg, PO Wits, 2050, South Africa
                [2 ]Vertebrate Department, Ditsong National Museum of Natural History, PO Box 413, Pretoria, 0001, South Africa
                Article
                10.1655/HERPETOLOGICA-D-16-00055
                b2b22517-e4b8-4263-9f8d-393bd7b525d8
                © 2017

                http://www.bioone.org/page/resources/researchers/rights_and_permissions

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