用户名: 密码: 验证码:
Reproductive strategy and carry-over effects for species with complex life histories
详细信息    查看全文
  • 作者:Adam W. Green (1)
    Larissa L. Bailey (1)

    1. Department of Fish
    ; Wildlife ; and Conservation Biology ; Colorado State University ; 1474 Campus Delivery ; Fort Collins ; CO ; 80523 ; USA
  • 关键词:Life history strategy ; Lithobates sylvatica ; Population dynamics ; Vernal pool ; Wood frog
  • 刊名:Population Ecology
  • 出版年:2015
  • 出版时间:January 2015
  • 年:2015
  • 卷:57
  • 期:1
  • 页码:175-184
  • 全文大小:458 KB
  • 参考文献:1. Aebischer, NJ, Wanless, S (1992) Relationships between colony size, adult non-breeding and environmental conditions for Shags Phalacrocorax aristotelis on the Isle of May, Scotland. Bird Study 39: pp. 43-52 CrossRef
    2. Altwegg, R, Reyer, HU (2003) Patterns of natural selection on size at metamorphosis in water frogs. Evolution 57: pp. 872-882 CrossRef
    3. Arnason, AN (1973) The estimation of population size, migration rates and survival in a stratified population. Res Popul Ecol 15: pp. 1-8 CrossRef
    4. Auer, SK, Lopez-Sepulcre, A, Heatherly, T, Kohler, TJ, Bassar, RD, Thomas, SA, Reznick, DN (2012) Life histories have a history: effects of past and present conditions on adult somatic growth rates in wild Trinidadian guppies. J Anim Ecol 81: pp. 818-826 CrossRef
    5. Bailey, LL, Kendall, WL, Church, DR, Wilbur, HM (2004) Estimating survival and breeding probability for pond-breeding amphibians: a modified robust design. Ecology 85: pp. 2456-2466 CrossRef
    6. Barbieri, MM, Berger, JO (2004) Optimal predictive model selection. Ann Stat 32: pp. 870-897 CrossRef
    7. Bastien, H, Leclair, R (1992) Aging wood frogs (Rana sylvatica) by skeletochronology. J Herpetol 26: pp. 222-225 CrossRef
    8. Beck, CW, Congdon, JD (1999) Effects of individual variation in age and size at metamorphosis on growth and survivorship of southern toad (Bufo terrestris) metamorphs. Can J Zool 77: pp. 944-951 CrossRef
    9. Berven, KA (1982) The genetic basis of altitudinal variation in the wood frog Rana sylvatica. 1. An experimental analysis of life history traits. Evolution 36: pp. 962-983 CrossRef
    10. Berven, KA (1988) Factors affecting variation in reproductive traits within a population of wood frogs (Rana sylvatica). Copeia 3: pp. 605-615 CrossRef
    11. Berven, KA (1990) Factors affecting population fluctuations in larval and adult stages of the wood frog (Rana sylvatica). Ecology 71: pp. 1599-1608 CrossRef
    12. Berven, KA (1995) Population regulation in the wood frog, Rana sylvatica, from three diverse geographic localities. Aust J Ecol 20: pp. 385-392 CrossRef
    13. Berven, KA, Chadra, BG (1988) The relationship among egg size, density and food level on larval development in the wood frog (Rana sylvatica). Oecologia 75: pp. 67-72 CrossRef
    14. Berven, KA, Grudzien, TA (1990) Dispersal in the wood frog (Rana sylvatica): implications for genetic population structure. Evolution 44: pp. 2047-2056 CrossRef
    15. Biek, R, Funk, WC, Maxell, BA, Mills, LS (2002) What is missing in amphibian decline research: insights from ecological sensitivity analysis. Conserv Biol 16: pp. 728-734 CrossRef
    16. Boekelheide, RJ, Ainley, DG (1989) Age, resource availability, and breeding effort in Brandt鈥檚 Cormorant. Auk 106: pp. 389-401
    17. Boone, MD (2005) Juvenile frogs compensate for small metamorph size with terrestrial growth: overcoming the effects of larval density and insecticide exposure. J Herpetol 39: pp. 416-423 CrossRef
    18. Breden, F (1987) The effect of post-metamorphic dispersal on the population genetic structure of Fowler鈥檚 toad, Bufo woodhousei fowleri. Copeia 1987: pp. 386-395 CrossRef
    19. Burnham, KP, Anderson, DR (2002) Model selection and multimodel inference: a practical information-theoretic approach. Springer, New York
    20. Chelgren, ND, Rosenberg, DK, Heppell, SS, Gitelman, AI (2006) Carryover aquatic effects on survival of metamorphic frogs during pond emigration. Ecol Appl 16: pp. 250-261 CrossRef
    21. Church, DR, Bailey, LL, Wilbur, HM, Kendall, WL, Hines, JE (2007) Iteroparity in the variable environment of the salamander Ambystoma tigrinum. Ecology 88: pp. 891-903 CrossRef
    22. Conroy, SDS, Brook, BW (2003) Demographic sensitivity and persistence of the threatened white- and orange-bellied frogs of Western Australia. Popul Ecol 45: pp. 105-114 CrossRef
    23. Converse, SJ, Kendall, WL, Doherty, PF, Ryan, PG (2009) Multistate models for estimation of survival and reproduction in the grey-headed albatross. Auk 126: pp. 77-88 CrossRef
    24. Cook, JG, Johnson, BK, Cook, RC, Riggs, RA, Delcurto, T, Bryant, LD, Irwin, LL (2004) Effects of summer-autumn nutrition and parturition date on reproduction and survival of elk. Wildlife Monogr 155: pp. 1-61
    25. Boer, PJ (1968) Spreading of risk and stabilization of animal numbers. Acta Biotheor A 17: pp. 165-194 CrossRef
    26. Festa-Bianchet, M, Gaillard, JM, Jorgenson, JT (1998) Mass- and density-dependent reproductive success and reproductive costs in a capital breeder. Am Nat 152: pp. 367-379 CrossRef
    27. Gillespie, JH (1974) Natural selection for within-generation variance in offspring number. Genetics 76: pp. 601-606
    28. Hamilton, SL, Regetz, J, Warner, RR (2008) Postsettlement survival linked to larval life in a marine fish. P Natl Acad Sci USA 105: pp. 1561-1566 CrossRef
    29. Harrison, XA, Blount, JD, Inger, R, Norris, DR, Bearhop, S (2010) Carry-over effects as drivers of fitness differences in animals. J Anim Ecol 80: pp. 4-18 CrossRef
    30. Hels, T, Nachman, G (2002) Simulating viability of a spadefoot toad Pelobates fuscus metapopulation in a landscape fragmented by a road. Ecography 25: pp. 730-744 CrossRef
    31. Hettinger, A, Sanford, E, Hill, TM, Russell, AD, Sato, KNS, Hoey, J, Forsch, M, Page, HN, Gaylord, B (2012) Persistent carry-over effects of planktonic exposure to ocean acidification in the Olympia oyster. Ecology 93: pp. 2758-2768 CrossRef
    32. Hopey, ME, Petranka, JW (1994) Restriction of wood frogs to fish-free habitats: how important is adult choice?. Copeia 1994: pp. 1023-1025 CrossRef
    33. John-Alder, HB, Morin, PJ (1990) Effects of larval density on jumping ability and stamina in newly metamorphosed Bufo woodhousii fowleri. Copeia 1990: pp. 856-860 CrossRef
    34. Karraker, NE, Gibbs, JP, Vonesh, JR (2008) Impacts of road deicing salt on the demography of vernal pool-breeding amphibians. Ecol Appl 18: pp. 724-734 CrossRef
    35. Kendall, WL (1999) Robustness of closed capture-recapture methods to violations of the closure assumption. Ecology 80: pp. 2517-2525
    36. Kendall, WL, Nichols, JD (2002) Estimating state-transition probabilities for unobservable states using capture-recapture/resighting data. Ecology 83: pp. 3276-3284
    37. Kendall, WL, Nichols, JD, Hines, JE (1997) Estimating temporary emigration using capture-recapture data with Pollock鈥檚 robust design. Ecology 78: pp. 563-578
    38. Lampo, M, Leo, GA (1998) The invasion ecology of the toad Bufo marinus: from South America to Australia. Ecol Appl 8: pp. 388-396
    39. Langtimm, CA (2009) Non-random temporary emigration and the robust design: conditions for bias at the end of a time series. Environ Ecol Stat 3: pp. 745-761
    40. Lebreton, JD, Nichols, JD, Barker, RJ, Pradel, R, Spendelow, JA (2009) Modeling individual animal histories with multistate mark-recapture models. Adv Ecol Res 41: pp. 87-173 CrossRef
    41. Lichko, LE, Calhoun, AJK (2003) An evaluation of vernal pool creation projects in New England: project documentation from 1991鈥?000. Environ Manage 32: pp. 141-151 CrossRef
    42. Licht, LE (1974) Survival of embryos, tadpoles, and adults of the frogs Rana aurora and Rana pretiosa sympatric in southwestern British Columbia. Can J Zool 52: pp. 613-627 CrossRef
    43. Madsen, T, Shine, R (2000) Silver spoons and snake body sizes: prey availability early in life influences long-term growth rates of free-ranging pythons. J Anim Ecol 69: pp. 952-958 CrossRef
    44. Martof, BS, Humphries, RL (1959) Geographic variation in the wood frog Rana sylvatica. Am Midl Nat 61: pp. 350-389 CrossRef
    45. Morey, S, Reznick, D (2001) Effects of larval density on postmetamorphic spadefoot toads (Spea hammondii). Ecology 82: pp. 510-522 CrossRef
    46. Muths, E, Scherer, RD, Lambert, BA (2010) Unbiased survival estimates and evidence for skipped breeding opportunities in females. Method Ecol Evol 2010: pp. 123-130 CrossRef
    47. Nichols, JD, Hines, JE, Sauer, JR, Fallon, FW, Fallon, JE, Heglund, PJ (2000) A double-observer approach for estimating detection probability and abundance from point counts. Auk 117: pp. 292-408 CrossRef
    48. Norris, DR, Taylor, CM (2006) Predicting the consequences of carry-over effects for migratory populations. Biol Lett 2: pp. 148-151 CrossRef
    49. Norris, DR, Marra, PP, Kyser, TK, Sherry, TW, Ratcliffe, LM (2004) Tropical winter habitat limits reproductive success on the temperate breeding grounds in a migratory bird. P Roy Soc Lond B Biol 271: pp. 59-64 CrossRef
    50. Pechmann, JHK, Estes, RA, Scott, DE, Gibbons, JW (2001) Amphibian colonization and use of ponds created for trial mitigation of wetland loss. Wetlands 21: pp. 93-111 CrossRef
    51. Phillips, NE (2002) Effects of nutrition-mediated larval condition on juvenile performance in a marine mussel. Ecology 83: pp. 2562-2574 CrossRef
    52. Quinn, TP (2011) The behavior and ecology of Pacific salmon and trout. University of British Columbia Press, Vancouver
    53. Ray, C (1958) Vital limits and rates of desiccation in salamanders. Ecology 39: pp. 75-83 CrossRef
    54. Regosin, JV, Windmiller, BS, Reed, JM (2003) Terrestrial habitat use and winter densities of the wood frog (Rana sylvatica). J Herpetol 37: pp. 390-394 CrossRef
    55. Richardson, JI, Bell, R, Richardson, T (1999) Population ecology and demographic implications drawn from an 11-year study of nesting hawksbill turtles, Eretmochelys imbricate, at Jumby Bay, Long Island, Antigua, West Indies. Chelonian Conserv Biol 3: pp. 244-250
    56. Rittenhouse, TAG, Semlitsch, RD (2007) Postbreeding habitat use of wood frogs in a Missouri oak-hickory forest. J Herpetol 41: pp. 645-653 CrossRef
    57. Rittenhouse, TAG, Harper, EB, Rehard, LR, Semlitsch, RD (2008) The role of microhabitats in the desiccation and survival of anurans in recently harvested oak-hickory forest. Copeia 2008: pp. 807-814 CrossRef
    58. Rittenhouse, TAG, Semlitsch, RD, Thompson, FR (2009) Survival costs associated with wood frog breeding migrations: effects of timber harvest and drought. Ecology 90: pp. 1620-1630 CrossRef
    59. Rothermel, BB, Semlitsch, RD (2006) Consequences of forest fragmentation for juvenile survival in spotted (Ambystoma maculatum) and marbled (Ambystoma opacum) salamanders. Can J Zoolog 84: pp. 797-807 CrossRef
    60. Sanzo, D, Hecnar, SJ (2006) Effects of road de-icing salt (NaCl) on larval wood frogs (Rana sylvatica). Environ Pollut 140: pp. 247-256 CrossRef
    61. Schmidt, BR, H枚dl, W, Schaub, M (2012) From metamorphosis to maturity in complex life cycles: equal performance of different juvenile life history pathways. Ecology 93: pp. 657-667 CrossRef
    62. Scott, DE (1994) The effect of larval density on adult demographic traits in Ambystoma opacum. Ecology 75: pp. 1383-1396 CrossRef
    63. Semlitsch, RD, Wilbur, HM (1988) Effects of pond drying time on metamorphosis and survival in the salamander Ambystoma talpoideum. Copeia 1988: pp. 978-983 CrossRef
    64. Semlitsch, RD, Scott, DE, Pechmann, JHK (1988) Time and size at metamorphosis related to adult fitness in Ambystoma talpoideum. Ecology 69: pp. 184-192 CrossRef
    65. Skelly, DK, Freidenburg, LK, Kiesecker, JM (2002) Forest canopy and the performance of larval amphibians. Ecology 83: pp. 983-992 CrossRef
    66. Slatkin, M (1974) Hedging one鈥檚 evolutionary bets. Nature 250: pp. 704-705
    67. Smith, DC (1987) Recruitment in chorus frogs: effects of size and date at metamorphosis. Ecology 68: pp. 344-350 CrossRef
    68. Sorensen, MC, Hipfner, JM, Kyser, TK, Norris, DR (2009) Carry-over effects in a Pacific seabird: stable isotope evidence that pre-breeding diet quality influences reproductive success. J Anim Ecol 78: pp. 460-467 CrossRef
    69. Thorson, TB (1955) The relationship of water economy to terrestrialism in amphibians. Ecology 36: pp. 100-116 CrossRef
    70. Meter, R, Bailey, LL, Grant, EHC (2008) Methods for estimating the amount of vernal pool habitat in the northeastern United States. Wetlands 28: pp. 585-593 CrossRef
    71. Vonesh, JR, Cruz, O (2002) Complex life cycles and density dependence: assessing the contribution of egg mortality to amphibian declines. Oecologia 133: pp. 325-333 CrossRef
    72. Werner, EE, Glennemeier, KS (1999) Influence of forest canopy cover on the breeding pond distributions of several amphibian species. Copeia 1999: pp. 1-12 CrossRef
    73. White, GC, Burnham, KP (1999) Program MARK: survival estimation from populations of marked animals. Bird Study 46: pp. 120-139 CrossRef
    74. Wilbur, HM (1977) Interactions of food level and population density in Rana sylvatica. Ecology 58: pp. 206-209 CrossRef
    75. Wilbur, HM (1980) Complex life cycles. Annu Rev Ecol Syst 11: pp. 67-93 CrossRef
    76. Wilbur, HM, Rudolf, VHW (2006) Life-history evolution in uncertain environments: bet hedging in time. Am Nat 168: pp. 398-411 CrossRef
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Ecology
    Zoology
    Plant Sciences
    Evolutionary Biology
    Behavioural Sciences
    Forestry
  • 出版者:Springer Japan
  • ISSN:1438-390X
文摘
We investigated the influences of natal-pool and metamorph characteristics on juvenile survival, age-specific breeding probabilities, and dispersal of wood frogs (Lithobates sylvatica) and used this information to infer how life history strategies of short-lived species may offset risks associated with breeding in highly variable habitats. We used multistate mark-recapture data from eight wood frog populations in Maryland, USA, to investigate the influences of natal-pond and metamorph characteristics on post-metamorphic demographics. We found that post-metamorphic juvenile survival was highly variable and negatively influenced by abiotic conditions experienced during development but showed little relationship to larval density or size at metamorphosis. Estimates of recruitment and dispersal probabilities indicated that males mature earlier than females, and a small percentage of each sex disperse to non-natal pools. Survival probabilities for adults during the non-breeding season were less variable than juvenile rates, lower for females, and negatively related to mean monthly precipitation. Survival of adults during the breeding season was generally very high. We provide the first robust estimates of post-metamorphic vital rates of wood frogs that allow for variation in capture probabilities. We found little evidence for an effect of metamorph traits on juvenile survival, suggesting that wood frogs may be able to overcome initial disadvantages to have similar post-metamorphic performance. Our study suggests that variation in the age of maturity for wood frogs may mitigate risks associated with breeding in a highly variable habitat to maximize lifetime fitness without increasing lifespan, and this strategy is minimally affected by carry-over effects from the larval stage.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700