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Stress hormone metabolites predict overwinter survival in yellow-bellied marmots

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Abstract

Biological assays of stress, in particular noninvasive measures, are valuable tools for wildlife management. Chronic stress can have negative impacts on fitness outcomes, and an area of particular interest is if elevated baseline stress levels are predictive of survival outcomes. We examined the relationship between fecal glucocorticoid metabolites (FGMs) measured from samples collected during routine trapping and overwinter survival in a wild population of yellow-bellied marmots (Marmota flaviventris). In particular, we asked if elevated FGMs were associated with reduced survival probability. Both higher yearly FGM levels averaged over several months and higher late season FGM levels averaged over the several weeks before hibernation were associated with lower probability of survival. Additionally, there was an interaction between late-season FGM levels and body mass, such that the association between late-season FGMs and survival was much stronger in animals with lower body mass (i.e., in poorer condition). This study highlights the promise of using stress hormone metabolites, a noninvasive measure, for studying factors affecting survival in this and potentially other natural wildlife systems.

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References

  • Andersen DC, Armitage KB, Hoffmann RS (1976) Socioecology of marmots: female reproductive strategies. Ecology 57(3):552–560. doi:10.2307/1936439

    Article  Google Scholar 

  • Armitage KB (1991) Factors affecting corticosteroid concentrations in yellow-bellied marmots. Comp Biochem Physiol A Physiol 98(1):47–54

    Article  CAS  Google Scholar 

  • Armitage KB (2003) Marmots: Marmota monax and allies. In: Feldhamer GA, Thompson BC (eds) Wild mammals of North America, 2nd edn. The Johns Hopkins University Press, Baltimore, p 1216

    Google Scholar 

  • Bates D, Maechler M, Bolker B (2013) lme4: linear mixed-effects models using S4 classes. R package version 0.999999-2 edn

  • Blumstein DT, Lea AJ, Olson LE, Martin J (2010) Heritability of anti-predatory traits: vigilance and locomoter performance in marmots. J Evol Biol 23:879–887

    Article  CAS  PubMed  Google Scholar 

  • Bonier F, Martin PR, Moore IT, Wingfield JC (2009) Do baseline glucocorticoids predict fitness? Trends Ecol Evol 24(11):634–642. doi:10.1016/j.tree.2009.04.013

    Article  PubMed  Google Scholar 

  • Boonstra R, Singleton GR (1993) Population declines in the snowshoe hare and the role of stress. Gen Comp Endocrinol 91(2):126–143. doi:10.1006/gcen.1993.1113

    Article  CAS  PubMed  Google Scholar 

  • Crawley MJ (2007) The R book. John Wiley & Sons, West Sussex

    Book  Google Scholar 

  • Ebensperger LA, Tapia D, Ramírez-Estrada J, León C, Soto-Gamboa M, Hayes LD (2013) Fecal cortisol levels predict breeding but not survival of females in the short-lived rodent, Octodon degus. Gen Comp Endocrinol 186:164–171. doi:10.1016/j.ygcen.2013.02.044

    Article  CAS  PubMed  Google Scholar 

  • Goymann W, Wingfield JC (2004) Allostatic load, social status and stress hormones: the costs of social status matter. Anim Behav 67(3):591–602. doi:10.1016/j.anbehav.2003.08.007

    Article  Google Scholar 

  • Harper JM, Austad SN (2000) Fecal glucocorticoids: a noninvasive method of measuring adrenal activity in wild and captive rodents. Physiol Biochem Zool 73(1):12–22

    Article  CAS  PubMed  Google Scholar 

  • Johnstone CP, Reina RD, Lill A (2012) Interpreting indices of physiological stress in free-living vertebrates. J Comp Physiol B 182(7):861–879. doi:10.1007/s00360-012-0656-9

    Article  PubMed  Google Scholar 

  • Kalinowski ST, Taper ML, Marshall TC (2007) Revising how the computer program CERVUS accommodates genotyping error increases success in paternity assignment. Mol Ecol 16:1099–1106

    Article  PubMed  Google Scholar 

  • Kasl SV (1984) Stress and health. Annu Rev Public Health 5:319–341

    Article  CAS  PubMed  Google Scholar 

  • Korte SM, Koolhaas JM, Wingfield JC, McEwen BS (2005) The Darwinian concept of stress: benefits of allostasis and costs of allostatic load and the trade-offs in health and disease. Neurosci Biobehav Rev 29(1):3–38. doi:10.1016/j.neubiorev.2004.08.009

    Article  PubMed  Google Scholar 

  • Lenihan C, Van Vuren D (1996) Growth and survival of juvenile yellow-bellied marmots (Marmota flaviventris). Can J Zool 74(2):297–302. doi:10.1139/z96-037

    Article  Google Scholar 

  • McEwen BS (1998) Stress, adaptation, and disease: allostasis and allostatic load. Ann N Y Acad Sci 840(1):33–44. doi:10.1111/j.1749-6632.1998.tb09546.x

    Article  CAS  PubMed  Google Scholar 

  • Millspaugh JJ, Washburn BE (2004) Use of fecal glucocorticoid metabolite measures in conservation biology research: considerations for application and interpretation. Gen Comp Endocrinol 138:189–199

    Article  CAS  PubMed  Google Scholar 

  • Möstl E, Palme R (2002) Hormones as indicators of stress. Domest Anim Endocrinol 23(1–2):67–74. doi:10.1016/S0739-7240(02)00146-7

    Article  PubMed  Google Scholar 

  • Pride RE (2005) High fecal glucocorticoid levels predict mortality in ring-tailed lemurs (Lemur catta). Biol Lett 1:60–63

    Article  CAS  Google Scholar 

  • R Core Team (2013) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna

    Google Scholar 

  • Reeder DM, Kramer KM (2005) Stress in free-ranging mammals: integrating physiology, ecology, and natural history. J Mammal 86(2):225–235

    Article  Google Scholar 

  • Rogovin KO, Randall JA, Kolosova I, Moshkin M (2003) Social correlates of stress in adult males of the great gerbil, Rhombomys opimus, in years of high and low population densities. Horm Behav 43(1):132–139. doi:10.1016/S0018-506X(02)00028-4

    Article  PubMed  Google Scholar 

  • Rogovin KA, Randall JA, Kolosova IE, Moshkin MP (2008) Long-term dynamics of fecal corticosterone in male great gerbils (Rhombomys opimus Licht.): effects of environment and social demography. Physiol Biochem Zool 81(5):612–626. doi:10.1086/588757

    Article  PubMed  Google Scholar 

  • Romero LM, Wikelski M (2001) Corticosterone levels predict survival probabilities of Galápagos marine iguanas during El Niño events. Proc Natl Acad Sci U S A 98:7366–7370

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Romero LM, Wikelski M (2010) Stress physiology as a predictor of survival in Galapagos marine iguanas. Proc R Soc B Biol Sci 277(1697):3157–3162. doi:10.1098/rspb.2010.0678

    Article  Google Scholar 

  • Sapolsky RM, Romero LM, Munck AU (2000) How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions. Endocr Rev 21(1):55–89

    CAS  PubMed  Google Scholar 

  • Schwartz OA, Armitage KB, Van Vuren D (1998) A 32-year demography of yellow-bellied marmots (Marmota flaviventris). J Zool 246(3):337–346. doi:10.1111/j.1469-7998.1998.tb00163.x

    Article  Google Scholar 

  • Schwarzenberger F (2007) The many uses of non-invasive faecal steroid monitoring in zoo and wildlife species. Int Zoo Yearb 41:52–74

    Article  Google Scholar 

  • Smith JE, Monclús R, Wantuck D, Florant GL, Blumstein DT (2012) Fecal glucocorticoid metabolites in wild yellow-bellied marmots: experimental validation, individual differences and ecological correlates. Gen Comp Endocrinol 178(2):417–426. doi:10.1016/j.ygcen.2012.06.015

    Article  CAS  PubMed  Google Scholar 

  • Wingfield JC (2005) The concept of allostasis: coping with a capricious environment. J Mammal 86(2):248–254. doi:10.1644/bhe-004.1

    Article  Google Scholar 

Download references

Acknowledgments

Funding during the work was provided by a US Department of Education GAANN Fellowship, a UCLA Chancellor’s Prize, an RMBL Snyder Graduate Research Fellowship, and a Bartholomew Research Grant (to Wey); the National Geographic Society, the Rocky Mountain Biological Laboratory, the Unisense foundation, a UCLA Faculty Senate Faculty Research Grants, the US National Science Foundation (IDBR 0754247, DEB-1119660), and UCLA Division of Life Sciences Dean’s recruitment and retention funds (to Blumstein); and NSF-DBI-0242960 and NSF-DBI-0731346 (to the RMBL). We thank Rebecca Nelson Booth for radioimmunoassay at the University of Washington Center for Conservation Biology, Jennifer E. Smith for fecal glucocorticoid metabolite measure validation and analysis, Adriana Maldonado-Chaparro and Julien G. A. Martin for data management, and many research assistants and the RMBL for making this work possible. We also thank the editor Ana Silva and two anonymous reviewers for the comments on a previous version of this manuscript.

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Correspondence to Tina W. Wey.

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Wey, T.W., Lin, L., Patton, M.L. et al. Stress hormone metabolites predict overwinter survival in yellow-bellied marmots. acta ethol 18, 181–185 (2015). https://doi.org/10.1007/s10211-014-0204-6

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  • DOI: https://doi.org/10.1007/s10211-014-0204-6

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