Analyze Diet
Ecology and evolution2022; 12(9); e9325; doi: 10.1002/ece3.9325

Non-native grazers affect physiological and demographic responses of greater sage-grouse.

Abstract: Non-native ungulate grazing has negatively impacted native species across the globe, leading to massive loss of biodiversity and ecosystem services. Despite their pervasiveness, interactions between non-native grazers and native species are not fully understood. We often observe declines in demography or survival of these native species, but lack understanding about the mechanisms underlying these declines. Physiological stress represents one mechanism of (mal)adaptation, but data are sparse. We investigated glucocorticoid levels in a native avian herbivore exposed to different intensities of non-native grazing in the cold desert Great Basin ecosystem, USA. We measured corticosterone, a glucocorticoid in feathers for a large sample ( = 280) of female greater sage-grouse () from three study areas in Northern Nevada and Southern Oregon with different grazing regimes of livestock and feral horses. We found that greater feral horse density was associated with higher corticosterone levels, and this effect was exacerbated by drought conditions. Livestock grazing produced similar results; however, there was more model uncertainty about the livestock effect. Subsequent nesting success was lower with increased feather corticosterone, but corticosterone levels were not predictive of other vital rates. Our results indicate a physiological response by sage-grouse to grazing pressure from non-native grazers. We found substantial among-individual variation in the strength of the response. These adverse effects were intensified during unfavorable weather events, highlighting the need to reevaluate management strategies in the face of climate change.
Publication Date: 2022-09-20 PubMed ID: 36188508PubMed Central: PMC9490135DOI: 10.1002/ece3.9325Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The study investigates how non-native grazing animals impact the native avian species, greater sage-grouse, in the cold desert Great Basin ecosystem in the USA. It specifically measures a stress hormone in the bird, finding that higher densities of non-native grazers correlate with increased stress levels in the sage-grouse, particularly during drought conditions.

Study Overview

  • The research was focused on understanding the impact of non-native grazers such as livestock and feral horses on the physiology and demography of greater sage-grouse in the Great Basin ecosystem in the USA.
  • The study examined the levels of corticosterone, a glucocorticoid often associated with stress, in the feathers of sage-grouse exposed to different grazing intensities.

Methods and Findings

  • The team measured corticosterone levels in a large sample of female sage-grouse from three study areas in Northern Nevada and Southern Oregon. These areas had varying livestock and feral horse population sizes.
  • The findings showed that higher densities of non-native grazers, especially feral horses, were linked to increased corticosterone levels in the sage-grouse. This response was found to be more intense during periods of drought.
  • Similarly, livestock grazing also resulted in increased corticosterone levels. However, the results were not as definitive as with the feral horses.
  • The study showed that higher corticosterone levels resulted in lower nesting success rates for the sage-grouse. However, these levels did not seem to influence other vital rates in the bird’s life cycle.

Conclusions

  • The study concludes that grazing pressure from non-native animals induces a physiological stress response in the greater sage-grouse, as evident by elevated corticosterone levels in these birds.
  • The researchers also noted significant variation among individual birds in the strength of this physiological response.
  • Importantly, the study also highlights that the negative effects of non-native grazing on sage-grouse are amplified during periods of unfavorable weather conditions, such as droughts. This points to potential implications for ecosystem management strategies in a changing climate.

Cite This Article

APA
Behnke T, Street P, Davies S, Ouyang JQ, Sedinger JS. (2022). Non-native grazers affect physiological and demographic responses of greater sage-grouse. Ecol Evol, 12(9), e9325. https://doi.org/10.1002/ece3.9325

Publication

ISSN: 2045-7758
NlmUniqueID: 101566408
Country: England
Language: English
Volume: 12
Issue: 9
Pages: e9325
PII: e9325

Researcher Affiliations

Behnke, Tessa
  • Program in Ecology, Evolution, and Conservation Biology University of Nevada-Reno Reno Nevada USA.
  • Department of Natural Resources and Environmental Science University of Nevada-Reno Reno Nevada USA.
Street, Phillip
  • Department of Natural Resources and Environmental Science University of Nevada-Reno Reno Nevada USA.
Davies, Scott
  • Department of Biological Sciences Quinnipiac University Hamden Connecticut USA.
Ouyang, Jenny Q
  • Program in Ecology, Evolution, and Conservation Biology University of Nevada-Reno Reno Nevada USA.
Sedinger, James S
  • Department of Natural Resources and Environmental Science University of Nevada-Reno Reno Nevada USA.

Conflict of Interest Statement

The authors declare no commercial or financial relationships generating a conflict of interest in this work.

References

This article includes 105 references
  1. Atamian MT, Sedinger JS, Heaton JS, Blomberg EJ. Landscape‐level assessment of brood rearing habitat for greater sage‐grouse in Nevada. Journal of Wildlife Management 74(7), 1533–1543.
    doi: 10.2193/2009-226google scholar: lookup
  2. Batchelor JL, Ripple WJ, Wilson TM, Painter LE. Restoration of riparian areas following the removal of cattle in the northwestern great basin.. Environ Manage 2015 Apr;55(4):930-42.
    doi: 10.1007/s00267-014-0436-2pubmed: 25694035google scholar: lookup
  3. Batzer DP, Baldwin AH. Wetland habitats of North America: Ecology and conservation concerns. .
  4. Baur LE, Schoenecker KA, Smith MD. Effects of feral horse herds on rangeland plant communities across a precipitation gradient. Western North American Naturalist 77(4), 526–540.
    doi: 10.3398/064.077.0412google scholar: lookup
  5. Beck JL, Mitchell DL. Influences of livestock grazing on sage grouse habitat. Wildlife Society Bulletin 28(4), 993–1002.
  6. Beever EA, Herrick JE. Effects of feral horses in Great Basin landscapes on soils and ants: Direct and indirect mechanisms. Journal of Arid Environments 66(1), 96–112.
  7. Behnke TL. Impacts of non‐native ungulate grazing on reproduction and physiology in Greater Sage‐grouse. .
  8. Beschta RL, Kauffman JB, Dobkin DS, Ellsworth LM. Long‐term livestock grazing alters aspen age structure in the northwestern Great Basin. Forest Ecology and Management 329, 30–36.
  9. Blomberg EJ, Gibson D, Atamian MT, Sedinger JS. Individual and environmental effects on egg allocations of female greater sage‐grouse. The Auk 131(4), 507–523.
    doi: 10.1642/auk-14-32.1google scholar: lookup
  10. Blomberg EJ, Gibson D, Atamian MT, Sedinger JS. Variable drivers of primary versus secondary nesting; density‐dependence and drought effects on greater sage‐grouse. Journal of Avian Biology 48(6), 827–836.
    doi: 10.1111/jav.00988google scholar: lookup
  11. Blomberg EJ, Poulson SR, Sedinger JS, Gibson D. Prefledging diet is correlated with individual growth in greater sage‐grouse (Centrocercus urophasianus). The Auk 130(4), 715–724.
    doi: 10.1525/auk.2013.12188google scholar: lookup
  12. Blomberg EJ, Sedinger JS, Atamian MT, Nonne DV. Characteristics of climate and landscape disturbance influence the dynamics of greater sage‐grouse populations. Ecosphere 3(6), 20.
    doi: 10.1890/es11-00304.1google scholar: lookup
  13. Blomberg EJ, Sedinger JS, Gibson D, Coates PS, Casazza ML. Carryover effects and climatic conditions influence the postfledging survival of greater sage-grouse.. Ecol Evol 2014 Dec;4(23):4488-99.
    doi: 10.1002/ece3.1139pmc: PMC4264898pubmed: 25512845google scholar: lookup
  14. Blomberg EJ, Sedinger JS, Nonne DV, Atamian MT. Seasonal reproductive costs contribute to reduced survival of female greater sage‐grouse. Journal of Avian Biology 44(2), 149–158.
  15. Blomberg EJ, Sedinger JS, Nonne DV, Atamian MT. Annual male lek attendance influences count‐based population indices of greater sage‐grouse. Journal of Wildlife Management 77(8), 1583–1592.
    doi: 10.1002/jwmg.615google scholar: lookup
  16. Bonier F, Moore IT, Martin PR, Robertson RJ. The relationship between fitness and baseline glucocorticoids in a passerine bird.. Gen Comp Endocrinol 2009 Sep 1;163(1-2):208-13.
    doi: 10.1016/j.ygcen.2008.12.013pubmed: 19135999google scholar: lookup
  17. Bortolotti GR, Marchant T, Blas J, Cabezas S. Tracking stress: localisation, deposition and stability of corticosterone in feathers.. J Exp Biol 2009 May;212(Pt 10):1477-82.
    doi: 10.1242/jeb.022152pubmed: 19411541google scholar: lookup
  18. Bortolotti GR, Marchant TA, Blas J, German T. Corticosterone in feathers is a long‐term, integrated measure of avian stress physiology. Functional Ecology 22(3), 494–500.
  19. Boyd CS, Beck JL, Tanaka JA. Livestock grazing and sage‐grouse habitat: Impacts and opportunities. Journal of Rangeland Applications 1, 58–77.
  20. Boyd CS, Davies KW, Collins GH. Impacts of feral horse use on herbaceous riparian vegetation within a sagebrush steppe ecosystem. Rangeland Ecology & Management 70(4), 411–417.
  21. Boyte SP, Wylie BK, Major DJ. Validating a time series of annual grass percent cover in the sagebrush ecosystem. Rangeland Ecology & Management 72(2), 347–359.
  22. Bradford JB, Schlaepfer DR, Lauenroth WK, Palmquist KA. Robust ecological drought projections for drylands in the 21st century.. Glob Chang Biol 2020 Jul;26(7):3906-3919.
    doi: 10.1111/gcb.15075pubmed: 32342577google scholar: lookup
  23. Braun CE, Dunn PO, Wann GT, Schroeder MA, Hupp JW. Body mass and primary molt patterns of greater sage‐grouse in Colorado. Western North American Naturalist 80(3), 330–336.
    doi: 10.3398/064.080.0304google scholar: lookup
  24. . BLM National Wild Horse and burro herd area and herd management area. Bureau of Land Management .
  25. . Livestock grazing on public lands. Bureau of Land Management .
  26. Byrnes RC, Eastburn DJ, Tate KW, Roche LM. A Global Meta-Analysis of Grazing Impacts on Soil Health Indicators.. J Environ Qual 2018 Jul;47(4):758-765.
    doi: 10.2134/jeq2017.08.0313pubmed: 30025044google scholar: lookup
  27. Casazza ML, Coates PS, Overton CT. Linking habitat selection and brood success in greater sage‐grouse. Ecology, Conservation, and Management of Grouse. Studies in Avian Biology 39, 151–167.
    doi: 10.1525/9780520950573google scholar: lookup
  28. Chambers JC, Blank RR, Zamudio DC, Tausch RJ. Central Nevada riparian areas: Physical and chemical properties of meadow soils. Journal of Range Management 52(1), 92–99.
    doi: 10.2307/4003497google scholar: lookup
  29. Coates PS, Prochazka BG, O'Donnell MS, Aldridge CL, Edmunds DR, Monroe AP, Ricca MA, Wann GT, Hanser SE, Wiechman LA, Chenaille M. Range‐wide greater sage‐grouse hierarchical monitoring framework—Implications for defining population boundaries, trend estimation, and a targeted annual warning system (2331–1258). US Geological Survey .
    doi: 10.3133/ofr20201154google scholar: lookup
  30. Cockrem JF. Stress, corticosterone responses and avian personalities. Journal of Ornithology 148(2), 169–178.
    doi: 10.1007/s10336-007-0175-8google scholar: lookup
  31. Cockrem JF. Corticosterone responses and personality in birds: Individual variation and the ability to cope with environmental changes due to climate change.. Gen Comp Endocrinol 2013 Sep 1;190:156-63.
    doi: 10.1016/j.ygcen.2013.02.021pubmed: 23467071google scholar: lookup
  32. Crossin GT, Phillips RA, Lattin CR, Romero LM, Williams TD. Corticosterone mediated costs of reproduction link current to future breeding.. Gen Comp Endocrinol 2013 Nov 1;193:112-20.
    doi: 10.1016/j.ygcen.2013.07.011pubmed: 23891657google scholar: lookup
  33. Crunden CW. Age and sex of sage grouse from wings. Journal of Wildlife Management 27, 846–850.
    doi: 10.2307/3798498google scholar: lookup
  34. Cyr NE, Michael Romero L. Chronic stress in free-living European starlings reduces corticosterone concentrations and reproductive success.. Gen Comp Endocrinol 2007 Mar;151(1):82-9.
    doi: 10.1016/j.ygcen.2006.12.003pubmed: 17280663google scholar: lookup
  35. Dahlgren DK, Larsen RT, Danvir R, Wilson G, Thacker ET, Black TA, Naugle DE, Connelly JW, Messmer TA. Greater sage‐grouse and range management: Insights from a 25‐year case study in Utah and Wyoming. Rangeland Ecology & Management 68(5), 375–382.
  36. Dettenmaier SJ, Messmer TA, Hovick TJ, Dahlgren DK. Effects of livestock grazing on rangeland biodiversity: A meta-analysis of grouse populations.. Ecol Evol 2017 Oct;7(19):7620-7627.
    doi: 10.1002/ece3.3287pmc: PMC5632623pubmed: 29043019google scholar: lookup
  37. Dobkin DS, Rich AC, Pyle WH. Habitat and avifaunal recovery from livestock grazing in a riparian meadow system of the northwestern Great Basin. Conservation Biology 12(1), 209–221.
  38. Donnelly JP, Allred BW, Perret D, Silverman NL, Tack JD, Dreitz VJ, Maestas JD, Naugle DE. Seasonal drought in North America's sagebrush biome structures dynamic mesic resources for sage-grouse.. Ecol Evol 2018 Dec;8(24):12492-12505.
    doi: 10.1002/ece3.4614pmc: PMC6308899pubmed: 30619560google scholar: lookup
  39. Donnelly JP, Naugle DE, Hagen CA, Maestas JD. Public lands and private waters: Scarce Mesic resources structure land tenure and sage‐grouse distributions. Ecosphere 7(1), e01208.
    doi: 10.1002/ecs2.1208google scholar: lookup
  40. Eldridge DJ, Ding J, Travers SK. Feral horse activity reduces environmental quality in ecosystems globally. Biological Conservation 241, 108367.
  41. Fairhurst GD, Champoux L, Hobson KA, Rail JF, Verreault J, Guillemette M, Montevecchi WA, Brousseau P, Soos C. Feather corticosterone during non-breeding correlates with multiple measures of physiology during subsequent breeding in a migratory seabird.. Comp Biochem Physiol A Mol Integr Physiol 2017 Jun;208:1-13.
    doi: 10.1016/j.cbpa.2017.02.024pubmed: 28242285google scholar: lookup
  42. Fischer RA, Apa AD, Wakkinen WL, Reese KP, Connelly JW. Nesting‐area fidelity of sage grouse in southeastern Idaho. The Condor 95(4), 1038–1041.
    doi: 10.2307/1369442google scholar: lookup
  43. Freeman S, Jackson WM. Univariate metrics are not adequate to measure avian body size. The Auk 107(1), 69–74.
    doi: 10.1093/auk/107.1.69google scholar: lookup
  44. Frye GG, Connelly JW, Musil DD, Forbey JS. Phytochemistry predicts habitat selection by an avian herbivore at multiple spatial scales.. Ecology 2013 Feb;94(2):308-14.
    doi: 10.1890/12-1313.1pubmed: 23691650google scholar: lookup
  45. Garrott RA. Wild horse demography: Implications for sustainable management within economic constraints. Human–Wildlife Interactions 12(1), 7.
    doi: 10.26077/z7w0-0w34google scholar: lookup
  46. Gibson D, Blomberg EJ, Atamian MT, Sedinger JS. Nesting habitat selection influences nest and early offspring survival in greater sage‐grouse. The Condor 118(4), 689–702.
    doi: 10.1650/condor-16-62.1google scholar: lookup
  47. Gibson RM, Bradbury JW. Lek organization in sage grouse: Variations on a territorial theme. The Auk 104(1), 77–84.
    doi: 10.2307/4087236google scholar: lookup
  48. Giesen KM, Schoenberg TJ, Braun CE. Methods for trapping sage grouse in Colorado. Wildlife Society Bulletin 10, 224–231.
  49. Gittleman JL, Kot M. Adaptation: Statistics and a null model for estimating phylogenetic effects. Systematic Zoology 39, 227–241.
    doi: 10.2307/2992183google scholar: lookup
  50. Graham SP, Freidenfelds NA, McCormick GL, Langkilde T. The impacts of invaders: basal and acute stress glucocorticoid profiles and immune function in native lizards threatened by invasive ants.. Gen Comp Endocrinol 2012 May 1;176(3):400-8.
    doi: 10.1016/j.ygcen.2011.12.027pubmed: 22226759google scholar: lookup
  51. Gregg MA, Barnett JK, Crawford JA. Temporal variation in diet and nutrition of preincubating greater sage‐grouse. Rangeland Ecology & Management 61(5), 535–542.
    doi: 10.2111/08-037.1google scholar: lookup
  52. Gregg MA, Crawford JA. Survival of greater sage‐grouse chicks and broods in the northern Great Basin. Journal of Wildlife Management 73(6), 904–913.
    doi: 10.2193/2007-410google scholar: lookup
  53. Hanley TA, Hanley KA. Food resource partitioning by sympatric ungulates on Great Basin rangeland. Rangeland Ecology & Management 35(2), 152–158.
  54. Hansen WK, Bate LJ, Landry DW, Chastel O, Parenteau C, Breuner CW. Feather and faecal corticosterone concentrations predict future reproductive decisions in harlequin ducks (Histrionicus histrionicus).. Conserv Physiol 2016;4(1):cow015.
    doi: 10.1093/conphys/cow015pmc: PMC4922300pubmed: 27382474google scholar: lookup
  55. Harms NJ, Legagneux P, Gilchrist HG, Bêty J, Love OP, Forbes MR, Bortolotti GR, Soos C. Feather corticosterone reveals effect of moulting conditions in the autumn on subsequent reproductive output and survival in an Arctic migratory bird.. Proc Biol Sci 2015 Feb 7;282(1800):20142085.
    doi: 10.1098/rspb.2014.2085pmc: PMC4298207pubmed: 25540279google scholar: lookup
  56. Hau M, Ricklefs RE, Wikelski M, Lee KA, Brawn JD. Corticosterone, testosterone and life-history strategies of birds.. Proc Biol Sci 2010 Oct 22;277(1697):3203-12.
    doi: 10.1098/rspb.2010.0673pmc: PMC2982062pubmed: 20554550google scholar: lookup
  57. Henderson LJ, Evans NP, Heidinger BJ, Herborn KA, Arnold KE. Do glucocorticoids predict fitness? Linking environmental conditions, corticosterone and reproductive success in the blue tit, Cyanistes caeruleus.. R Soc Open Sci 2017 Oct;4(10):170875.
    doi: 10.1098/rsos.170875pmc: PMC5666270pubmed: 29134087google scholar: lookup
  58. Hooten MB, Hobbs NT. A guide to Bayesian model selection for ecologists. Ecological Monographs 85(1), 3–28.
    doi: 10.1890/14-0661.1google scholar: lookup
  59. Huntington JL, Hegewisch KC, Daudert B, Morton CG, Abatzoglou JT, McEvoy DJ, Erickson T. Climate engine: Cloud computing and visualization of climate and remote sensing data for advanced natural resource monitoring and process understanding. Bulletin of the American Meteorological Society 98(11), 2397–2410.
    doi: 10.1175/BAMS-D-15-00324.1google scholar: lookup
  60. Injaian AS, Francis CD, Ouyang JQ, Dominoni DM, Donald JW, Fuxjager MJ, Goymann W, Hau M, Husak JF, Johnson MA, Kircher BK, Knapp R, Martin LB, Miller ET, Schoenle LA, Williams TD, Vitousek MN. Baseline and stress-induced corticosterone levels across birds and reptiles do not reflect urbanization levels.. Conserv Physiol 2020;8(1):coz110.
    doi: 10.1093/conphys/coz110pmc: PMC6978728pubmed: 31993201google scholar: lookup
  61. Jankowski MD, Russell RE, Franson JC, Dusek RJ, Hines MK, Gregg M, Hofmeister EK. Corticosterone metabolite concentrations in greater sage‐grouse are positively associated with the presence of cattle grazing. Rangeland Ecology & Management 67(3), 237–246.
    doi: 10.2111/rem-d-13-00137.1google scholar: lookup
  62. Johns DW, Marchant TA, Fairhurst GD, Speakman JR, Clark RG. Biomarker of burden: Feather corticosterone reflects energetic expenditure and allostatic overload in captive waterfowl. Functional Ecology 32(2), 345–357.
    doi: 10.1111/1365-2435.12988google scholar: lookup
  63. Kane K, Sedinger JS, Gibson D, Blomberg EJ, Atamian MT. Fitness landscapes and life table response experiments predict the importance of local areas to population dynamics. Ecosphere 8, e01869.
  64. Kellner K. jagsUI: A wrapper around rjags to streamline JAGS analyses. R package version 1(1).
  65. King SR, Schoenecker KA, Manier DJ. Potential spread of cheatgrass and other invasive species by feral horses in western Colorado. Rangeland Ecology & Management 72(4), 706–710.
  66. Koren L, Nakagawa S, Burke T, Soma KK, Wynne-Edwards KE, Geffen E. Non-breeding feather concentrations of testosterone, corticosterone and cortisol are associated with subsequent survival in wild house sparrows.. Proc Biol Sci 2012 Apr 22;279(1733):1560-6.
    doi: 10.1098/rspb.2011.2062pmc: PMC3282351pubmed: 22090380google scholar: lookup
  67. Madliger CL, Love OP. Conservation implications of a lack of relationship between baseline glucocorticoids and fitness in a wild passerine.. Ecol Appl 2016 Dec;26(8):2730-2743.
    doi: 10.1002/eap.1401pubmed: 27763712google scholar: lookup
  68. Monclus L, Carbajal A, Tallo-Parra O, Sabes-Alsina M, Darwich L, Molina-Lopez RA, Lopez-Bejar M. Relationship between feather corticosterone and subsequent health status and survival in wild Eurasian Sparrowhawk. Journal of Ornithology 158(3), 773–783.
    doi: 10.1007/s10336-016-1424-5google scholar: lookup
  69. Monroe AP, Aldridge CL, Assal TJ, Veblen KE, Pyke DA, Casazza ML. Patterns in Greater Sage-grouse population dynamics correspond with public grazing records at broad scales.. Ecol Appl 2017 Jun;27(4):1096-1107.
    doi: 10.1002/eap.1512pubmed: 28329422google scholar: lookup
  70. Narayan EJ, Jessop TS, Hero J. Invasive cane toad triggers chronic physiological stress and decreased reproductive success in an Island endemic. Functional Ecology 29(11), 1435–1444.
    doi: 10.1111/1365-2435.12446google scholar: lookup
  71. . NDOW Greater Sage‐Grouse Population Management Units [GIS data set]. .
  72. Plummer M. JAGS: A program for analysis of Bayesian graphical models using Gibbs sampling. Proceedings of the 3rd international workshop on distributed statistical computing 124(125.10), 1–10.
  73. . PRISM climate data. .
  74. R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing .
  75. Remington TE, Braun CE. Sage grouse food selection in winter, North Park, Colorado. Journal of Wildlife Management 49, 1055–1061.
    doi: 10.2307/3801395google scholar: lookup
  76. Rich EL, Romero LM. Exposure to chronic stress downregulates corticosterone responses to acute stressors.. Am J Physiol Regul Integr Comp Physiol 2005 Jun;288(6):R1628-36.
    doi: 10.1152/ajpregu.00484.2004pubmed: 15886358google scholar: lookup
  77. Romero LM. Physiological stress in ecology: lessons from biomedical research.. Trends Ecol Evol 2004 May;19(5):249-55.
    doi: 10.1016/j.tree.2004.03.008pubmed: 16701264google scholar: lookup
  78. Rowland MM, Wisdom MJ, Suring LH, Meinke CW. Greater sage‐grouse as an umbrella species for sagebrush‐associated vertebrates. Biological Conservation 129(3), 323–335.
  79. Royle JA, Dorazio RM. Hierarchical modeling and inference in ecology: The analysis of data from populations, metapopulations and communities. Elsevier Science .
  80. Santicchia F, Dantzer B, van Kesteren F, Palme R, Martinoli A, Ferrari N, Wauters LA. Stress in biological invasions: Introduced invasive grey squirrels increase physiological stress in native Eurasian red squirrels.. J Anim Ecol 2018 Sep;87(5):1342-1352.
    doi: 10.1111/1365-2656.12853pubmed: 29790583google scholar: lookup
  81. Sapolsky RM, Romero LM, Munck AU. How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions.. Endocr Rev 2000 Feb;21(1):55-89.
    doi: 10.1210/edrv.21.1.0389pubmed: 10696570google scholar: lookup
  82. Scasta JD, Beck JL, Angwin CJ. Meta‐analysis of diet composition and potential conflict of wild horses with livestock and wild ungulates on western rangelands of North America. Rangeland Ecology & Management 69(4), 310–318.
  83. Schroeder MA, Young JR, Braun CE. Greater sage‐grouse (Centrocercus urophasianus). Birds of the world 1st ed..
  84. Sedinger JS. Adaptations to and consequences of an herbivorous diet in grouse and waterfowl. The Condor 99(2), 314–326.
    doi: 10.2307/1369937google scholar: lookup
  85. Smith KT, Pratt AC, LeVan JR, Rhea AM, Beck JL. Reconstructing greater sage‐grouse chick diets: Diet selection, body condition, and food availability at brood‐rearing sites. The Condor: Ornithological Applications 121(1), duy012.
    doi: 10.1093/condor/duy012google scholar: lookup
  86. Snyder KA, Evers L, Chambers JC, Dunham J, Bradford JB, Loik ME. Effects of changing climate on the hydrological cycle in cold desert ecosystems of the Great Basin and Columbia plateau. Rangeland Ecology & Management 72(1), 1–12.
  87. Sorenson GH, Dey CJ, Madliger CL, Love OP. Effectiveness of baseline corticosterone as a monitoring tool for fitness: a meta-analysis in seabirds.. Oecologia 2017 Feb;183(2):353-365.
    doi: 10.1007/s00442-016-3774-3pubmed: 27873067google scholar: lookup
  88. Souchay G, Gauthier G, Pradel R. To breed or not: A novel approach to estimate breeding propensity and potential trade‐offs in an Arctic‐nesting species. Ecology 95(10), 2745–2756.
    doi: 10.1890/13-1277.1google scholar: lookup
  89. Spear D, Chown SL. Non‐indigenous ungulates as a threat to biodiversity. Journal of Zoology 279(1), 1–17.
  90. Street PA. Greater sage‐grouse habitat and demographic response to grazing by non‐native ungulates. .
  91. Street PA, Riecke TV, Williams PJ, Behnke TL, Sedinger JS. Estimating survival and adoption rates of dependent juveniles.. Ecol Evol 2022 Jul;12(6):e9005.
    doi: 10.1002/ece3.9005pmc: PMC9203589pubmed: 35784036google scholar: lookup
  92. . Hart Mountain National Antelope Refuge. U.S. Fish and Wildlife Service .
  93. . Sheldon National Wildlife Refuge. U.S. Fish and Wildlife Service .
  94. Van Zwol JA, Neff BD, Wilson CC. The influence of non‐native salmonids on circulating hormone concentrations in juvenile Atlantic salmon. Animal Behaviour 83(1), 119–129.
  95. Veblen KE, Nehring KC, McGlone CM, Ritchie ME. Contrasting effects of different mammalian herbivores on sagebrush plant communities.. PLoS One 2015;10(2):e0118016.
  96. Vera F, Zenuto R, Antenucci CD. Expanding the actions of cortisol and corticosterone in wild vertebrates: A necessary step to overcome the emerging challenges.. Gen Comp Endocrinol 2017 May 15;246:337-353.
    doi: 10.1016/j.ygcen.2017.01.010pubmed: 28109824google scholar: lookup
  97. Volery L, Jatavallabhula D, Scillitani L, Bertolino S, Bacher S. Ranking alien species based on their risks of causing environmental impacts: a global assessment of alien ungulates.. Glob Chang Biol 2020 Dec 1;.
    doi: 10.1111/gcb.15467pubmed: 33289257google scholar: lookup
  98. Warren JM, Cutting KA, Takekawa JY, De La Cruz SE, Williams TD, Koons DN. Previous success and current body condition determine breeding propensity in lesser scaup: Evidence for the individual heterogeneity hypothesis. The Auk: Ornithological Advances 131(3), 287–297.
    doi: 10.1642/AUK-13-236.1google scholar: lookup
  99. Will A, Watanuki Y, Kikuchi DM, Sato N, Ito M, Callahan M, Wynne-Edwards K, Hatch S, Elliott K, Slater L, Takahashi A, Kitaysky A. Feather corticosterone reveals stress associated with dietary changes in a breeding seabird.. Ecol Evol 2015 Oct;5(19):4221-32.
    doi: 10.1002/ece3.1694pmc: PMC4667832pubmed: 26664674google scholar: lookup
  100. Williams CT, Kitaysky AS, Kettle AB, Buck CL. Corticosterone levels of tufted puffins vary with breeding stage, body condition index, and reproductive performance.. Gen Comp Endocrinol 2008 Aug;158(1):29-35.
    doi: 10.1016/j.ygcen.2008.04.018pubmed: 18547575google scholar: lookup
  101. Williamson MA, Fleishman E, Mac Nally RC, Chambers JC, Bradley BA, Dobkin DS, Board DI, Fogarty FA, Horning N, Leu M, Wohlfeil Zillig M. Fire, livestock grazing, topography, and precipitation affect occurrence and prevalence of cheatgrass (Bromus tectorum) in the central Great Basin, USA. Biological Invasions 22(2), 663–680.
  102. Wingfield JC, Hunt K, Breuner C, Dunlap K, Fowler GS, Freed L, Lepson J. Environmental stress, field endocrinology, and conservation biology. Behavioral approaches to conservation in the wild pp. 95–131.
  103. Wingfield JC, Pérez JH, Krause JS, Word KR, González-Gómez PL, Lisovski S, Chmura HE. How birds cope physiologically and behaviourally with extreme climatic events.. Philos Trans R Soc Lond B Biol Sci 2017 Jun 19;372(1723).
    doi: 10.1098/rstb.2016.0140pmc: PMC5434091pubmed: 28483870google scholar: lookup
  104. Wingfield JC, Sapolsky RM. Reproduction and resistance to stress: when and how.. J Neuroendocrinol 2003 Aug;15(8):711-24.
  105. Zeigenfuss LC, Schoenecker KA, Ransom JI, Ignizio DA, Mask T. Influence of nonnative and native ungulate biomass and seasonal precipitation on vegetation production in a Great Basin ecosystem. Western North American Naturalist 74(3), 286–298.

Citations

This article has been cited 0 times.