dc.contributor.author | Włodarczyk, Radosław | |
dc.contributor.author | Minias, Piotr | |
dc.date.accessioned | 2021-09-07T13:06:24Z | |
dc.date.available | 2021-09-07T13:06:24Z | |
dc.date.issued | 2020 | |
dc.identifier.citation | Włodarczyk, R., Minias, P. Age-related differences in reproductive success support the selection hypothesis in a Mute Swan population. J Ornithol 161, 1185–1193 (2020). https://doi.org/10.1007/s10336-020-01803-7 | pl_PL |
dc.identifier.issn | 2193-7192 | |
dc.identifier.uri | http://hdl.handle.net/11089/38997 | |
dc.description.abstract | In many bird species, we observe age-related differences in reproductive success, which usually increases early in life and later decreases due to senescence. At the individual level, an early-life improvement in breeding performance may be associated with experience acquired during early reproductive events (experience hypothesis). At the population level, higher average reproductive success of older age cohorts can result from a disappearance of low-quality individuals from the population (selection hypothesis). Here, we tested these hypotheses in a wild population of the Mute Swan Cygnus olor from central Poland. In 1996–2016, we collected information on breeding success of 150 marked individuals (70 females and 80 males; 590 breeding attempts). At the population level, there was an initial increase in reproductive success (1–5 years), followed by a plateau (5–8 years), and then by a decrease in older age classes. Both within- and between-individual age variation contributed to the linear increase in reproductive success at the population level, but the latter effect was much more apparent. Short-term breeders (≤ 2 breeding events) had significantly lower reproductive success than long-term breeders (≥ 3 breeding events) during their first two breeding attempts, providing support for selection hypothesis and disappearance of low-quality phenotypes. After exclusion of short-term breeders, a positive age-related increase in reproductive success lost significance, suggesting that under-specific condition (rapid population growth and strong human disturbance) experience may have a limited effect on reproductive success in long-lived species with strong pair bonds, such as the Mute Swan. | pl_PL |
dc.description.abstract | Für viele Vogelarten stellen wir altersbedingte Unterschiede im Reproduktionserfolg fest, der normalerweise in der Jugend anwächst und später im Alter wieder nachlässt. Auf individueller Ebene ist eine Verbesserung der Brutleistung in der Jugend möglicherweise mit Erfahrungen aus frühen Fortpflanzungserlebnissen verbunden (Erfahrungshypothese). Auf Populationsebene könnte ein höherer Reproduktionserfolg älterer Altersgruppen aus dem Verschwinden von Individuen minderer Qualität resultieren (Selektionshypothese). Wir untersuchten beide Hypothesen an einer wildlebenden Höckerschwan-Population (Cygnus olor) in Zentralpolen. Von 1996 bis 2016 sammelten wir Informationen zum Bruterfolg von 150 markierten Einzeltieren (70 Weibchen und 80 Männchen; 590 Brutansätze). Auf Populationsebene gab es zunächst eine Zunahme des Bruterfolgs (1–5 Jahre), gefolgt von einem Plateau (5-8 Jahre) und dann einer Abnahme bei den älteren Jahrgängen. Die Altersschwankungen sowohl der einzelnen als auch zwischen den Tieren trugen zu einem linearen Anstieg des Reproduktionserfolgs auf der Populationsebene bei, wobei der Effekt der letzteren Gruppe aber der wesentlich größere war. Kurzzeit-Brütende (≤ 2 Brutansätze) hatten einen signifikant geringeren Bruterfolg als Langzeit-Brüter (≥ 3 Brutansätze) während ihrer ersten zwei Brutversuche, was die Selektionshypothese und das Verschwinden von Phenotypen geringerer Qualität unterstützt. Lässt man die Kurzzeit-Brüter aus der Rechnung heraus, verliert der positive, altersbedingte Anstieg des Bruterfolgs an Bedeutung, was darauf hindeutet, dass unter bestimmten Bedingungen (rasches Wachsen der Population, starke Störungen durch Menschen) bei langlebigen Arten mit starker Paarbindung wie dem Höckerschwan Erfahrungen nur einen begrenzten Einfluss auf den Fortpflanzungserfolg haben könnten. | pl_PL |
dc.language.iso | en | pl_PL |
dc.publisher | Springer | pl_PL |
dc.relation.ispartofseries | Journal of Ornithology;161 | |
dc.rights | Uznanie autorstwa 4.0 Międzynarodowe | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject | age | pl_PL |
dc.subject | mute swan | pl_PL |
dc.subject | phenotype disappearance | pl_PL |
dc.subject | reproductive success | pl_PL |
dc.subject | selection hypothesis | pl_PL |
dc.title | Age‑related diferences in reproductive success support the selection hypothesis in a Mute Swan population | pl_PL |
dc.type | Article | pl_PL |
dc.page.number | 1185–1193 | pl_PL |
dc.contributor.authorAffiliation | Department of Biodiversity Studies and Bioeducation, Faculty of Biology and Environmental Protection, University of Łódź, Banacha 1/3, 90-237 Łódź, Poland | pl_PL |
dc.contributor.authorAffiliation | Department of Biodiversity Studies and Bioeducation, Faculty of Biology and Environmental Protection, University of Łódź, Banacha 1/3, 90-237 Łódź, Poland | pl_PL |
dc.identifier.eissn | 2193-7206 | |
dc.references | Angelier F, Weimerskirch H, Dano S, Chastel O (2007) Age, experience and reproductive performance in a long-lived bird: a hormonal perspective. Behav Ecol Sociobiol 61:611–621 | pl_PL |
dc.references | Auld JR, Perrins Ch, Charmantier A (2013) Who wears the pants in a mute swan pair? Deciphering the effects of male and female age and identity on breeding success. J Anim Ecol 82:826–835 | pl_PL |
dc.references | Baillie SR, Milne H (1982) The influence of female age on breeding in the Eider Somateria mollissima. Bird Study 29:55–66 | pl_PL |
dc.references | Berman M, Gaillard J-M, Weimerskirch H (2009) Contrasted patterns of age-specific reproduction in long-lived seabirds. Proc R Soc B 276:375–382 | pl_PL |
dc.references | Birkhead M, Perrins CM (1986) The mute swan. Croom Helm, London | pl_PL |
dc.references | Brown MJ, Linton E, Rees EC (1992) Causes of mortality among wild swans in Britain. Wildfowl 43:70–79 | pl_PL |
dc.references | Cam E, Monnat J-Y (2000) Stratification based on reproductive state reveals contrasting patterns of age-related variation in demographic parameters in the kittiwake. Oikos 90:560–574 | pl_PL |
dc.references | Charmantier A, Perrins CH, McCleery RH, Sheldon BC (2006) Age-dependent genetic variance in a life-history trait in the mute swan. Proc R Soc B 273:225–232 | pl_PL |
dc.references | Cichoń M (2003) Does prior breeding experience improve reproductive success in collared flycatcher females? Oecologia 134:78–81 | pl_PL |
dc.references | Clutton-Brock TH (1988) Reproductive Success. In: Clutton-Brock TH (ed) Reproductive success: studies of individual variation in contrasting breeding systems. University of Chicago Press, Chicago, pp 472–485 | pl_PL |
dc.references | Coleman AE, Coleman JT, Coleman PA, Minton CDT (2001) A 39 year study of a Mute Swan Cygnus olor population in the English Midlands. Ardea 89:113–121 | pl_PL |
dc.references | Collins R (2002) Sex differences in the movements and mortality of Mute Swans. In: Rees EC, Earnst S L, Coulson J (eds). Proceedings of the fourth international swan symposium; 2001. Waterbirds 25, Spec. Pub. 1:157–161 | pl_PL |
dc.references | Curio E (1983) Why do young birds reproduce less well? Ibis 125:400–404 | pl_PL |
dc.references | Espie RHM, Oliphant LW, James PC, Warkentin IG, Lieske DJ (2000) Age-dependent breeding performance in merlins (Falco columbarius). Ecology 81:3404–3415 | pl_PL |
dc.references | Forslund P, Pärt T (1995) Age and reproduction in birds-hypotheses and tests. Trends Ecol Evol 10:374–378 | pl_PL |
dc.references | Hamer KC, Furness RW (1991) Age-specific breeding performance and reproductive effort in Great Skuas Catharacta skua. J Anim Ecol 60:693–704 | pl_PL |
dc.references | Jenkins D, Newton I, Brown C (1976) Structure and dynamics of a mute swan population. Wildfowl 27:77–82 | pl_PL |
dc.references | Johannesen E, Houston D, Russell J (2003) Increased survival and breeding performance of double breeders in little penguins Eudyptula minor, New Zealand: evidence for individual bird quality? J Avian Biol 34:198–210 | pl_PL |
dc.references | Lehman A, O’Rourke N, Hatcher L, Stepanski EJ (2013) JMP® for basic univariate and multivariate statistics: methods for researchers and social scientists, 2nd edn. SAS Institute Inc., Cary | pl_PL |
dc.references | Limmer B, Becker PH (2009) Improvement in chick provisioning with parental experience in a seabird. Anim Behav 77:1095–1101 | pl_PL |
dc.references | Martin K (1995) Patterns and mechanisms for age-dependent reproduction and survival in birds. Am Zool 35:340–348 | pl_PL |
dc.references | Mauck RA, Huntington CE, Grubb TC (2004) Age-specific reproductive success: evidence for the selection hypothesis. Evolution 58:880–885 | pl_PL |
dc.references | McCleery RH, Perrins CM, Sheldon BC, Charmantier A (2008) Age-specific reproduction in a long-lived species: the combined effects of senescence and individual quality. Proc R Soc B 275:963–970 | pl_PL |
dc.references | Newton I (2008) The migration ecology of birds. Academic Press, London | pl_PL |
dc.references | Newton I, Rothery P (1998) Age-related trends in the breeding success of individual female Sparrowhawks Accipiter nisus. Ardea 86:21–31 | pl_PL |
dc.references | Perrins CM, McCleery RH (1997) Pairing behaviour in a colony of mute swans Cygnus olor. Wildfowl 47:31–41 | pl_PL |
dc.references | Perrins CM, McCleery RH, Ogilvie MA (1994) A study of the breeding Mute Swans Cygnus olor at Abbotsbury. Wildfowl 45:1–14 | pl_PL |
dc.references | Pyle P, Sydeman WJ, Hester M (2001) Effect of age, breeding experience, mate fidelity and site fidelity on breeding performance in a declining population of Cassin’s auklets. J Anim Ecol 70:1088–1097 | pl_PL |
dc.references | Raveling DG (1981) Survival, experience, and age in relation to breeding success of Canada Geese. J Wildlife Manage 45:817–829 | pl_PL |
dc.references | Rebke M, Coulson T, Becker PH, Vaupel JW (2010) Reproductive improvement and senescence in along-lived bird. Proc Natl Acad Sci USA 107:7841–7846 | pl_PL |
dc.references | Rees EC, Lievesley P, Pettifor RA, Perrins C (1996) Mate fidelity in swans: an interspecific comparison. In: Black J (ed) Partnerships in birds: the study of monogamy. Oxford University Press, Oxford, pp 118–138 | pl_PL |
dc.references | Robertson RJ, Rendell WB (2001) A long-term study of reproductive performance in tree swallows: the influence of age and senescence on output. J Anim Ecol 70:1014–1031 | pl_PL |
dc.references | Rockwell RF, Findlay CS, Cooke F (1983) Life history studies of the lesser snow goose (Anser caerulescens caerulescens). Oecologia 56:318–322 | pl_PL |
dc.references | Rose MR (1991) Evolutionary biology of ageing. Oxford Univ. Press, New York | pl_PL |
dc.references | Roughgarden J (1971) Density-dependent natural selection. Ecology 52:453–468 | pl_PL |
dc.references | Ruxton GD, Beauchamp G (2008) Time for some a priori thinking about post hoc testing. Behav Ecol 19:690–693 | pl_PL |
dc.references | Saino N, Ambrosini R, Martinnelli R, Møller AP (2002) Mate fidelity, senescence in breeding performance and reproductive trade-offs in the barn swallow. J Anim Ecol 71:309–319 | pl_PL |
dc.references | Satterthwaite FE (1946) An approximation distribution of estimates of variance components. Biomet Bull 2:110–114 | pl_PL |
dc.references | Scott DK (1984) Winter territoriality of mute swans Cygnus olor. Ibis 126:168–176 | pl_PL |
dc.references | Scott DK (1988) Reproductive success in Bewick’s Swans. In: Clutton-Brock TH (ed) Reproductive success: studies of individual variation in contrasting breeding systems. University of Chicago Press, Chicago, pp 220–236 | pl_PL |
dc.references | Sedinger JS, Flint PL, Lindberg MS (1995) Environmental Influence on Life-History Traits: growth, Survival, and Fecundity in Black Brant (Branta bernicla). Ecology 76:2404–2414 | pl_PL |
dc.references | Stearns SC (1992) The evolution of life histories. Oxford University Press, New York | pl_PL |
dc.references | Steenhof K, Heath JA (2009) American Kestrel reproduction: evidence for the selection hypothesis and the role of dispersal. Ibis 151:493–501 | pl_PL |
dc.references | Storch D, Frynta D (2000) Evolution of habitat selection: stochastic acquisition of cognitive clues? Evol Ecol 13:591–600 | pl_PL |
dc.references | van de Pol M, Wright J (2009) A simple method for distinguishing within- versus between-subject effects using mixed models. Anim Behav 77:753–758 | pl_PL |
dc.references | Weimerskirch H (1992) Reproductive effort in long-lived birds: age-specific patterns of condition, reproduction and survival in the wandering albatross. Oikos 64:464–473 | pl_PL |
dc.references | Weiß BM, Kotrschal K, Möstl E, Hirschenhauser K (2010) Social and life-history correlates of hormonal partner compatibility in greylag geese (Anser anser). Behav Ecol 21:138–143 | pl_PL |
dc.references | Wiebe KL, Martin K (1994) Growing old in the cold: environment, age and reproduction in two ptarmigan species. J Ornithol 135:385 | pl_PL |
dc.references | Wieloch M, Włodarczyk R, Czapulak A (2004) The mute swan Cygnus olor. BWP Update 6:1–48 | pl_PL |
dc.references | Włodarczyk R, Janiszewski T (2007) Abundance and distribution of the mute swan Cygnus olor in the Łódź region. Notatki Ornitologiczne 48:82–91 | pl_PL |
dc.references | Włodarczyk R, Minias P (2016) Non-adaptive territory selection by a bird with exceptionally long parental care. PeerJ 4:e1852 | pl_PL |
dc.references | Włodarczyk R, Wieloch M, Czyż S, Dolata P, Minias P (2013) Natal and breeding dispersal in Mute Swans Cygnus olor: influence of sex, mate switching and reproductive success. Acta Ornithol 48:237–244 | pl_PL |
dc.references | Wood KA, Stillman RA, Coombs T, McDonald C, Daunt F, O’Hare MT (2013) The role of season and social grouping on habitat use by mute swans (Cygnus olor) in a lowland river catchment. Bird Study 60:229–237 | pl_PL |
dc.references | Wood KA, Newth JL, Hilton GM, Nolet BA, Rees EC (2016) Inter-annual variability and long-term trends in breeding success in a declining population of migratory swans. J Avian Biol 47:597–609 | pl_PL |
dc.references | Woog F (2002) Reproductive success and pairing in Hawaiian Geese (Branta sandvicensis) in relation to age and body size. J Ornithol 143:43–50 | pl_PL |
dc.references | Zabala J, Zuberogoitia I (2015) Breeding performance and survival in the peregrine falcon Falco peregrinus support an age-related competence improvement hypothesis mediated via an age threshold. J Avian Biol 45:141–150 | pl_PL |
dc.identifier.doi | 10.1007/s10336-020-01803-7 | |
dc.discipline | nauki biologiczne | pl_PL |