Skip to main content
Log in

Demographic consequences of age-structure in extreme environments: population models for arctic and alpine ptarmigan

  • Population Ecology
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

Organisms living in arctic and alpine environments are increasingly impacted by human activities. To evaluate the potential impacts of global change, a better understanding of the demography of organisms in extreme environments is needed. In this study, we compare the age-specific demography of willow ptarmigan (Lagopus lagopus) breeding at arctic and subalpine sites, and white-tailed ptarmigan (L. leucurus) breeding at an alpine site. Rates of egg production improved with age at the alpine and subalpine sites, but the stochastic effects of nest and brood predation led to similar rates of annual fecundity among 1-, 2-, and 3+-year-old females. All populations had short generation times (T<2.7 years) and low net reproductive rates (R 0<1.2). Stable age distributions were weighted towards 1-year-old females in willow ptarmigan (>59%), and to 3+-year-old females in white-tailed ptarmigan (>47%). High damping ratios (ρ>3.2) indicated that asymptotic estimates were likely to match natural age distributions. Sensitivity and elasticity values indicated that changes in juvenile survival would have the greatest impact on the finite rate of population change (λ) in willow ptarmigan, whereas changes to the survival of 3+-year-old females would have a greater effect in white-tailed ptarmigan. High survivorship buffers white-tailed ptarmigan in alpine environments against the potential effects of climate change on annual fecundity, but may make the species more sensitive to the effects of pollutants or harvesting on adult survival. Conversely, processes that reduce annual fecundity would have a greater impact on the population viability of willow ptarmigan in arctic and subalpine environments. If these same demographic patterns prove to be widespread among organisms in extreme environments, it may be possible to develop general recommendations for conservation of the biological resources of arctic and alpine ecosystems.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Barbraud C, Weimerskirch H (2001) Emperor penguins and climate change. Nature 411:183–186

    Article  PubMed  CAS  Google Scholar 

  • Baur A, Baur B (1998) Altitudinal variation in size and composition of eggs in the land snail Arianta arbustorum. Can J Zool 76:2067–2074

    Article  Google Scholar 

  • Bergerud AT, Mossop DH, Myrberget S (1985) A critique of the mechanics of annual changes in ptarmigan numbers. Can J Zool 63:2240–2248

    Article  Google Scholar 

  • Berven KA (1982) The genetic basis of altitudinal variation in the wood frog Rana sylvatica. I. An experimental analysis of life history traits. Evolution 36:962–983

    Article  Google Scholar 

  • Blais JM, Schindler DW, Muir DCG, Kimpe LE, Donald DB, Rosenberg B (1998) Accumulation of persistent organochlorine compounds in mountains of western Canada. Nature 395:585–588

    Article  CAS  Google Scholar 

  • Blanckenhorn WU (1997) Altitudinal life history variation in the dung flies Scathophaga stercoraria and Sepsis cynipsea. Oecologia 109:342–352

    Article  Google Scholar 

  • Blomberg SP, Shine R (2001) Modelling life history strategies with capture-recapture data: evolutionary demography of the water skink Eulamprus tympanum. Austral Ecol 26:349–359

    Article  Google Scholar 

  • Blums P, Mednis A (1996) Secondary sex ratio in Anatinae. Auk 113:505–511

    Google Scholar 

  • Burnham KP, Anderson DR (1998) Model selection and inference: a practical information-theoretic approach. Springer-Verlag, New York

    Google Scholar 

  • Caizergues A, Ellison LN (1997) Survival of black grouse Tetrao tetrix in the French Alps. Wildlife Biology 3:177–186

    Google Scholar 

  • Caizergues A, Ellison LN (2000) Age-specific reproductive performance of black grouse Tetrao tetrix females. Bird Study 47:344–351

    Google Scholar 

  • Caswell H (2001) Matrix population models: construction, analysis, and interpretation. Sinauer Associates, Inc. Publishers, Sunderland, Massachusetts

    Google Scholar 

  • Chapin III FS, Körner C (1994) Arctic and alpine biodiversity: patterns, causes and ecosystem consequences. TREE 9:45–47

    Google Scholar 

  • Clarke JA, Johnson RE (1992) The influence of spring snow depth on white-tailed ptarmigan breeding success in the Sierra Nevada. Condor 94:622–627

    Article  Google Scholar 

  • Cooch E, Lank D, Robertson R, Cooke F (1997) Effects of parental age and environmental change on offspring sex ratio in a precocial bird. J Anim Ecol 66:189–202

    Article  Google Scholar 

  • Cooch E, Rockwell RF, Brault S (2001) Retrospective analysis of demographic responses to environmental change: a lesser snow goose example. Ecol Monogr 71:377–400

    Google Scholar 

  • Crone EE (2001) Is survivorship a better fitness surrogate than fecundity? Evolution 55:2611–2614

    PubMed  CAS  Google Scholar 

  • Derocher AE, Lunn NJ, Stirling I (2004) Polar bears in a warming climate. Integr Comp Biol 44:163–176

    Article  Google Scholar 

  • Dobson FS (1992) Body mass, structural size, and life-history patterns of the Columbian ground squirrel. Am Nat 139:109–125

    Article  Google Scholar 

  • Eriksen B, Molau U, Sevensson M (1993) Reproductive strategies in two arctic Pedicularis species (Scrophulariaceae). Ecography 16:154–166

    Article  Google Scholar 

  • Fieberg J, Ellner SP (2001) Stochastic matrix models for conservation and management: a comparative review of methods. Ecol Letters 4:244–266

    Article  Google Scholar 

  • Franken RJ, Hik DS (2004a) Influence of habitat quality, patch size and connectivity on colonization and extinction dynamics of collared pikas Ochotona collaris. J Anim Ecol 73:889–896

    Article  Google Scholar 

  • Franken RJ, Hik DS (2004b) Interannual variation in timing of parturition and growth of collared pikas Ochotona collaris in the southwest Yukon. Integr Comp Biol 44:186–193

    Article  Google Scholar 

  • Ganter B, Boyd H (2000) A tropical volcano, high predation pressure, and the breeding biology of arctic waterbirds: a circumpolar review of breeding failure in the summer of 1992. Arctic 53:289–305

    Google Scholar 

  • Giesen KM, Braun CE (1993) Natal dispersal and recruitment of juvenile white-tailed ptarmigan in Colorado. J Wildl Manage 57:72–77

    Article  Google Scholar 

  • Gould WR, Nichols JD (1998) Estimation of temporal variability of survival in animal populations. Ecology 79:2531–2538

    Google Scholar 

  • Gugerli F (1998) Effect of elevation on sexual reproduction in alpine populations of Saxifraga oppositifolia (Saxifragaceae). Oecologia 114:60–66

    Article  Google Scholar 

  • Gutiérrez RJ, Barrowclough GF, Groth JG (2000) A classification of the grouse (Aves: Tetroninae) based on mitochondrial DNA sequences. Wildlife Biology 6:205–211

    Google Scholar 

  • Hagen CA, Pitman JC, Sandercock BK, Robel RJ, Applegate RD (2005) Age-specific variation in apparent survival rates of male lesser prairie-chickens. Condor 107:78–86

    Article  Google Scholar 

  • Hannon SJ, Martin K (1996) Mate fidelity and divorce in ptarmigan: polygyny avoidance on the tundra. In: Black JM (eds) Partnerships in birds: the study of monogamy. Oxford University Press, Oxford, pp 192–210

    Google Scholar 

  • Hannon SJ, Smith JNM (1984) Factors influencing age-related reproductive success in the willow ptarmigan. Auk 101:848–854

    Google Scholar 

  • Hannon SJ, Eason PK, Martin K (1998) Willow ptarmigan (Lagopus lagopus). In: Poole A, Gill F (eds) The Birds of North America. The Birds of North America, Inc., Philadelphia, PA, pp 1–28

    Google Scholar 

  • Haydon DT, Gillis EA, Stefan CI, Krebs CJ (1999) Biases in the estimation of the demographic parameters of a snowshoe hare population. J Anim Ecol 68:501–512

    Article  Google Scholar 

  • Hines JE, Sauer JR (1989) Program CONTRAST: a general program for the analysis of several survival or recovery rate estimates. Fish and Wildlife Service Technical Report 24, Washington, DC

    Google Scholar 

  • Hitchcock C, Gratto-Trevor CL (1997) Diagnosing a shorebird local population decline with a stage-structured population model. Ecology 78:522–534

    Article  Google Scholar 

  • Hudson PJ (1992) Grouse in space and time: the population biology of a managed gamebird. The Game Conservancy Trust, Fordingbridge, United Kingdom

    Google Scholar 

  • Inouye DW, Barr B, Armitage KB, Inouye BD (2000) Climate change is affecting altitudinal migrants and hibernating species. Proc Nat Acad Sci USA 97:1630–1633

    Article  PubMed  CAS  Google Scholar 

  • Johnson KH, Braun CE (1999) Viability and conservation of an exploited sage grouse population. Cons Biol 13:77–84

    Article  Google Scholar 

  • Kelly BC, Gobas FAPC (2003) An arctic terrestrial food-chain bioaccumulation model for persistent organic pollutants. Environ Sci Technol 37:2966–2974

    Article  PubMed  CAS  Google Scholar 

  • Krajick K (2004) All downhill from here? Science 303:1600–1602

    Article  PubMed  CAS  Google Scholar 

  • Krementz DG, Handford P (1984) Does avian clutch size increase with altitude? Oikos 43:256–259

    Article  Google Scholar 

  • Larison JR, Likens GE, Fitzpatrick JW, Crock JG (2000) Cadmium toxicity among wildlife in the Colorado Rocky Mountains. Nature 406:181–183

    Article  PubMed  CAS  Google Scholar 

  • Møller AP, de Lope F (1999) Senescence in a short-lived migratory bird: age-dependent morphology, migration, reproduction and parasitism. J Anim Ecol 68:163–171

    Article  Google Scholar 

  • Mani MS (1968) Ecology and biogeography of high altitude insects. Dr. W. Junk N.V. Publishers, The Hague, Netherlands

    Google Scholar 

  • Martin K (2001) Wildlife in alpine and sub-alpine habitats. In: Johnson DH, O’Neil TA (eds) Wildlife-habitat relationships in Oregon and Washington. Oregon State University Press, Corvallis, Oregon, pp 285–310

    Google Scholar 

  • Martin K, Hannon SJ (1987) Natal philopatry and recruitment of willow ptarmigan in north central and northwestern Canada. Oecologia 71:518–524

    Article  Google Scholar 

  • Martin K, Wiebe KL (2004) Coping mechanisms of alpine and arctic breeding birds: extreme weather and limitations to reproductive resilience. Integr Comp Biol 44:97–105

    Article  Google Scholar 

  • Martin K, Hannon SJ, Rockwell RF (1989) Clutch size variation and patterns of attrition in fecundity of willow ptarmigan. Ecology 70:1788–1799

    Article  Google Scholar 

  • Martin K, Stacey PB, Braun CE (2000) Recruitment, dispersal, and demographic rescue in spatially-structured white-tailed ptarmigan populations. Condor 102:503–516

    Article  Google Scholar 

  • Mathworks (2000) Matlab, Ver. 6. Mathworks Inc., Natick, MA

  • Meats A (1971) The relative importance to population increase of fluctuations in mortality, fecundity and the time variables of the reproductive schedule. Oecologia 6:223–237

    Article  Google Scholar 

  • Morris WF, Doak DF (1998) Life history of the long-lived gynodioecious cushion plant Silene acaulis (Caryophyllaceae), inferred from size-based population projection matrices. Amer J Bot 85:784–793

    Article  Google Scholar 

  • Morris WF, Doak DF (2004) Buffering of life histories against environmental stochasticity: accounting for a spurious correlation between the variabilities of vital rates and their contributions to fitness. Am Nat 163:579–590

    Article  PubMed  Google Scholar 

  • Moss R, Watson A (2001) Population cycles in birds of the grouse family (Tetraonidae). Adv Ecol Res 32:53–111

    Google Scholar 

  • Moss R, Picozzi N, Summers RW, Baines D (2000) Capercaillie Tetrao urogallus in Scotland - demography of a declining population. Ibis 142:259–267

    Article  Google Scholar 

  • Myklebust I, Pedersen HC (1999) Accumulation and distribution of cadmium in willow ptarmigan. Ecotoxicology 8:457–465

    Article  CAS  Google Scholar 

  • Nichols JD, Hines JE (2002) Approaches for the direct estimation of λ, and demographic contributions to λ, using capture-recapture data. J Appl Stat 29:539–568

    Article  Google Scholar 

  • Orell M, Belda EJ (2002) Delayed cost of reproduction and senescence in the willow tit Parus montanus. J Anim Ecol 71:55–64

    Article  Google Scholar 

  • Parmesan C, Yohe G (2003) A globally coherent fingerprint of climate change impacts across natural systems. Nature 421:37–42

    Article  PubMed  CAS  Google Scholar 

  • Pedersen HC, Steen H, Kastdalen L, Brøseth H, Ims RA, Svendsen W, Yoccuz NG (2004) Weak compensation of harvest despite strong density-dependent growth in willow ptarmigan. Proc R Soc Lond B 271:381–385

    Article  CAS  Google Scholar 

  • Robb LA, Martin K, Hannon SJ (1992) Spring body condition, fecundity and survival in female willow ptarmigan. J Anim Ecol 61:215–233

    Article  Google Scholar 

  • Sandercock BK, Martin K, Hannon SJ (2005) Life history strategies in extreme environments: comparative demography of arctic and alpine ptarmigan. Ecology (in press)

  • SAS Institute (2000) SAS User’s Guide: Statistics, ver. 8. SAS Institute, Cary, NC

  • Schieck JO, Hannon SJ (1989) Breeding site fidelity in willow ptarmigan: the influence of previous reproductive success and familiarity with partner and territory. Oecologia 81:465–472

    Article  Google Scholar 

  • Schieck JO, Hannon SJ (1993) Clutch predation, cover and the overdispersion of nests of the willow ptarmigan. Ecology 74:743–750

    Article  Google Scholar 

  • Smith A, Willebrand T (1999) Mortality causes and survival rates of hunted and unhunted willow grouse. J Wildl Manage 63:722–730

    Article  Google Scholar 

  • Steen H, Erikstad KE (1996) Sensitivity of willow grouse Lagopus lagopus population dynamics to variations in demographic parameters. Wildlife Biology 2:27–35

    Google Scholar 

  • Tharme AP, Green RE, Baines D, Bainbridge IP, O’Brien M (2001) The effect of management for red grouse shooting on the population density of breeding birds on heather-dominated moorland. J Appl Ecol 38:439–457

    Article  Google Scholar 

  • Van Vuren D, Armitage KB (1991) Duration of snow cover and its influence on life-history variation in yellow-bellied marmots. Can J Zool 69:1755–1758

    Google Scholar 

  • Walther G-R, Post E, Convey P, Menzel A, Parmesan C, Beebee TJC, Fromentin J-M, Hoegh-Guldberg O, Bairlein F (2002) Ecological responses to recent climate change. Nature 416:389–395

    Article  PubMed  CAS  Google Scholar 

  • Wang G, Hobbs NT, Giesen KM, Galbraith H, Ojima DS, Braun CE (2002) Relationships between climate and population dynamics of white-tailed ptarmigan Lagopus leucurus in Rocky Mountain National Park, Colorado, USA. Climate Res 23:81–87

    Article  Google Scholar 

  • Watson A, Moss R (2004) Impacts of ski-development on ptarmigan (Lagopus mutus) at Cairn Gorm, Scotland. Biol Cons 116:267–275

    Article  Google Scholar 

  • Watson A, Moss R, Rothery P, Parr R (1984) Demographic causes and predictive models of population fluctuations in red grouse. J Anim Ecol 53:639–662

    Article  Google Scholar 

  • Watson A, Moss R, Rae S (1998) Population dynamics of Scottish rock ptarmigan cycles. Ecology 79:1174–1192

    Google Scholar 

  • White GC, Burnham KP (1999) Program MARK: survival estimation from populations of marked animals. Bird Study (Suppl) 46:S120-S139

    Google Scholar 

  • Wiebe KL, Martin K (1998a) Age-specific patterns of reproduction in white-tailed and willow ptarmigan Lagopus leucurus and L. lagopus. Ibis 140:14–24

    Article  Google Scholar 

  • Wiebe KL, Martin K (1998b) Costs and benefits of nest cover for ptarmigan: changes within and between years. Anim Behav 56:1137–1144

    Article  PubMed  Google Scholar 

  • Willebrand T (1992) Breeding and age in female black grouse Tetrao tetrix. Ornis Scand 23:29–32

    Article  Google Scholar 

  • Wisdom MJ, Mills LS (1997) Sensitivity analysis to guide population recovery: prairie-chickens as an example. J Wildl Manage 61:302–312

    Article  Google Scholar 

Download references

Acknowledgements

We thank the many field assistants and graduate students who worked hard to collect 26 years of demographic data under challenging field conditions. C.E. Braun and the Colorado Division of Wildlife provided logistical assistance for the white-tailed ptarmigan population study. The field research was financed by grants to the authors and F. Cooke from the Canadian Circumpolar Institute (NSTG and BAR grants), Canadian Wildlife Service, Natural Sciences and Engineering Research Council of Canada, Queen’s University, and the Universities of Alberta, British Columbia, Sherbrooke, and Toronto. B.K. Sandercock received financial support from the Killam Foundation at the University of British Columbia and the Division of Biology at Kansas State University during preparation of this article. We thank H.H. Bears, E. Cam, W.R. Clark, J.M. Reid, D.W. Roberts, C. Vleck, S. Wilson, and the two anonymous reviewers for constructive criticism of previous versions of the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Brett K. Sandercock.

Additional information

Communicated by Carol Vleck

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sandercock, B.K., Martin, K. & Hannon, S.J. Demographic consequences of age-structure in extreme environments: population models for arctic and alpine ptarmigan. Oecologia 146, 13–24 (2005). https://doi.org/10.1007/s00442-005-0174-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00442-005-0174-5

Keywords

Navigation