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Large increase in nest size linked to climate change: an indicator of life history, senescence and condition

  • Global change ecology - Original research
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Abstract

Many animals build extravagant nests that exceed the size required for successful reproduction. Large nests may signal the parenting ability of nest builders suggesting that nests may have a signaling function. In particular, many raptors build very large nests for their body size. We studied nest size in the goshawk Accipiter gentilis, which is a top predator throughout most of the Nearctic. Both males and females build nests, and males provision their females and offspring with food. Nest volume in the goshawk is almost three-fold larger than predicted from their body size. Nest size in the goshawk is highly variable and may reach more than 600 kg for a bird that weighs ca. 1 kg. While 8.5 % of nests fell down, smaller nests fell down more often than large nests. There was a hump-shaped relationship between nest volume and female age, with a decline in nest volume late in life, as expected for senescence. Clutch size increased with nest volume. Nest volume increased during 1977–2014 in an accelerating fashion, linked to increasing spring temperature during April, when goshawks build and start reproduction. These findings are consistent with nest size being a reliable signal of parental ability, with large nest size signaling superior parenting ability and senescence, and also indicating climate warming.

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References

  • Alabrudzinska J, Kalinski A, Slomczynski R, Wawrzyniak J, Zielinski P, Banbura J (2003) Effects of nest characteristics on breeding success of great tits Parus major. Acta Ornithol 38:151–154

    Article  Google Scholar 

  • Álvarez E, Barba E (2008) Nest quality in relation to adult bird condition and its impact on reproduction in great tits Parus major. Acta Ornithol 43:3–9

    Article  Google Scholar 

  • Becker WA (1984) Manual of quantitative genetics. Academic Enterprises, Pullman

    Google Scholar 

  • Broggi J, Senar JC (2009) Brighter great tit parents build bigger nests. Ibis 155:588–591

    Article  Google Scholar 

  • Cohen J (1988) Statistical power analysis for the behavioral sciences, 2nd edn. Lawrence Erlbaum, Hillsdale

    Google Scholar 

  • Collias NE, Collias EC (1984) Nest building and bird behavior. Princeton University Press, Princeton

    Book  Google Scholar 

  • Cramp S, Perrins CM (1977) The birds of the Western Palearctic. Oxford University Press, Oxford

    Google Scholar 

  • Cramp S, Simmons KEL (eds) (1980) The birds of the Western Palearctic, vol 2. Oxford University Press, Oxford

    Google Scholar 

  • Crossman CA, Rohwer VG, Martin PR (2011) Variation in the structure of bird nests between northern Manitoba and southeastern Ontario. PLoS ONE 6:19086

    Article  Google Scholar 

  • de Neve L, Soler JJ, Soler M, Perez-Contreras T (2004) Nest size predicts the effect of food supplementation to magpie nestlings on their immunocompetence: an experimental test of nest size indicating parental ability. Behav Ecol 15:1031–1036

    Article  Google Scholar 

  • Erbeling-Denk C, Trillmich F (1990) Das Mikroklima im Nistkasten und seine Auswirkungen auf die Nestlinge beim Star. J Ornithol 131:73–84

    Article  Google Scholar 

  • Falconer DS, Mackay TFC (1996) Introduction to quantitative genetics, 4th edn. Longman, New York

    Google Scholar 

  • Hall ZI, Street SE, Healy SD (2013) The evolution of cerebellum structure correlates with nest complexity. Biol Lett 9:20130687

    Article  PubMed Central  PubMed  Google Scholar 

  • Hansell MH (2000) Bird nests and construction behaviour. Cambridge University Press, Cambridge

    Book  Google Scholar 

  • Hansell MH (2007) Built by animals. Oxford University Press, Oxford

    Google Scholar 

  • Heenan CB, Seymour RS (2011) Structural support, not insulation, is the primary driver for avian cup-shaped nest design. Proc R Soc Lond B 278:2924–2929

    Article  Google Scholar 

  • Herfindal I, van de Pol M, Nielsen JT, Sæther B-E, Møller AP (2015) Climatic conditions cause complex patterns of covariation between demographic traits in a long-lived raptor. J Anim Ecol 84:702–711

    Article  PubMed  Google Scholar 

  • Holstein V (1942) Duehøgen. Hirschsprung, Copenhagen

    Google Scholar 

  • Kenward R (2006) The goshawk. Poyser, London

    Google Scholar 

  • Kern MD, Van Riper CIII (1984) Altitudinal variations in nests of the Hawaiian honeycreeper Hemignathus virens virens. Condor 86:443–454

    Article  Google Scholar 

  • Kühlapfel O, Brune J (1995) Die Mauserfeder als Hilfsmittel zur Altersbestimmung und Individualerkennung von Habichten (Accipiter gentilis). Charadrius 31:120–125

    Google Scholar 

  • Mainwaring MC, Hartley IR (2008) Seasonal adjustments in nest cup lining in blue tits Cyanistes caeruleus. Ardea 96:278–282

    Article  Google Scholar 

  • Mainwaring MC, Hartley IR, Bearhop S, Brulez K, du Feu CR, Murphy G, Plummer KE, Webber SL, Reynolds SJ, Deeming DC (2012) Latitudinal variation in blue tit and great tit nest characteristics indicates environmental adjustment. J Biogeogr 39:1669–1677

    Article  Google Scholar 

  • Mennerat A, Mirleau P, Blondel J, Perret P, Lambrecht M, Heeb P (2009) Aromatic plants in nests of the blue tit Cyanistes caeruleus protect chicks from bacteria. Oecologia 161:849–855

    Article  PubMed  Google Scholar 

  • Møller AP (1984) On the use of feathers in birds’ nests: predictions and tests. Ornis Scand 15:38–42

    Article  Google Scholar 

  • Møller AP (1990) Nest predation selects for small nest size in the blackbird. Oikos 57:237–240

    Article  Google Scholar 

  • Møller AP (2006) Rapid change in nest size of a bird related to change in a secondary sexual character. Behav Ecol 17:108–116

    Article  Google Scholar 

  • Møller AP, Nielsen JT (2014) Parental defense of offspring and life history of a long-lived raptor. Behav Ecol 25:1505–1512

    Article  Google Scholar 

  • Møller AP, Flensted-Jensen E, Klarborg K, Mardal W, Nielsen JT (2010) Climate change affects the duration of the reproductive season in birds. J Anim Ecol 79:777–784

    PubMed  Google Scholar 

  • Møller AP, Adriaensen F, Artemyev A, Bańbura J et al (2014a) Clutch size in European secondary hole-nesting passerines in relation to nest-box floor area, habitat, geographic location and study year. Methods Ecol Evol 5:353–362

    Article  Google Scholar 

  • Møller AP, Adriaensen F, Artemyev A, Bańbura J et al (2014b) Variation in clutch size in relation to nest size in birds. Ecol Evol 4:3583–3595

    Article  PubMed Central  PubMed  Google Scholar 

  • Newton I (2010) Population ecology of raptors. Black, London

    Google Scholar 

  • Nielsen JT, Drachmann J (2003) Age-dependent reproductive performance in Northern Goshawks Accipiter gentilis. Ibis 145:1–8

    Article  Google Scholar 

  • Nielsen JT, Møller AP (2006) Effects of food abundance, density and climate change on reproduction in the sparrowhawk Accipiter nisus. Oecologia 149:505–518

    Article  PubMed  Google Scholar 

  • Nord A, Sandell MI, Nilsson J-Å (2010) Female zebra finches compromise clutch temperature in energetically demanding incubation conditions. Funct Ecol 24:1031–1036

    Article  Google Scholar 

  • Nussey DH, Froy H, Lemaitre JF, Gaillard JM, Austad SN (2013) Senescence in natural populations of animals: widespread evidence and its implications for biogerontology. Ageing Res Rev 12:214–225

    Article  PubMed Central  PubMed  Google Scholar 

  • Opdam P, Müskens G (1976) Use of shed feathers in population studies of Accipiter hawks (Aves, Accipitriformes, Accipitridae). Beaufortia 24:55–62

    Google Scholar 

  • Peralta-Sánchez JM, Møller AP, Martín-Platero AM, Soler JJ (2010) Number and colour composition of nest lining feathers predict eggshell bacterial community in barn swallow nests: an experimental study. Funct Ecol 24:426–433

    Article  Google Scholar 

  • Sanz JJ, García-Navas V (2011) Nest ornamentation in blue tits: is feather carrying ability a male status signal? Behav Ecol 22:240–247

    Article  Google Scholar 

  • SAS (2012) JMP version 10.0. SAS Institute Inc, Cary

    Google Scholar 

  • Schaefer VH (1980) Geographic variation in the insulative qualities of nests of the northern oriole. Wilson Bull 92:466–474

    Google Scholar 

  • Slagsvold T (1982) Clutch size, nest size, and hatching asynchrony in birds: experiments with the fieldfare (Turdus pilaris). Ecology 63:1389–1399

    Article  Google Scholar 

  • Slagsvold T (1989) Experiments on clutch size and nest size in passerine birds. Oecologia 80:297–302

    Article  Google Scholar 

  • Soler JJ, Cuervo JJ, Møller AP, de Lope F (1998a) Nest building is a sexually selected behaviour in the barn swallow. Anim Behav 56:1435–1442

    Article  PubMed  Google Scholar 

  • Soler JJ, Møller AP, Soler M (1998b) Nest building, sexual selection and parental investment. Evol Ecol 12:427–441

    Article  Google Scholar 

  • Soler JJ, Martínez JG, Soler M, Møller AP (1999) Host sexual selection and cuckoo parasitism: an analysis of nest size in sympatric and allopatric magpie Pica pica populations parasitised by the great spotted cuckoo Clamator glandarius. Proc R Soc Lond B 266:1765–1771

    Article  Google Scholar 

  • Soler JJ, de Neve L, Martinez JG, Soler M (2001) Nest size affects clutch size and the start of incubation in magpies: an experimental study. Behav Ecol 12:301–307

    Article  Google Scholar 

  • Tomás G, Merino S, Martínez-de la Puente J, Moreno J, Morales J, Rivero-de-Aguilar J (2013) Nest size and aromatic plants in the nest as sexually selected female traits in blue tits. Behav Ecol 24:926–934

    Article  Google Scholar 

  • Tortosa FS, Redondo T (1992) Frequent copulations despite low sperm competition in white storks (Ciconia ciconia). Behaviour 121:288–315

    Article  Google Scholar 

  • Wimberger PH (1984) The use of green plant material in bird nests to avoid ectoparasites. Auk 101:615–618

    Google Scholar 

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Authors and Affiliations

  1. Laboratoire d’Ecologie, Systématique et Evolution, CNRS UMR 8079, Université Paris-Sud, Bâtiment 362, 91405, Orsay Cedex, France

    Anders Pape Møller

  2. Espedal 4, Tolne, 9870, Sindal, Denmark

    Jan Tøttrup Nielsen

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  1. Anders Pape Møller
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  2. Jan Tøttrup Nielsen
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Correspondence to Anders Pape Møller.

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Communicated by Indrikis Krams.

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Møller, A.P., Nielsen, J.T. Large increase in nest size linked to climate change: an indicator of life history, senescence and condition. Oecologia 179, 913–921 (2015). https://doi.org/10.1007/s00442-015-3385-4

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  • DOI: https://doi.org/10.1007/s00442-015-3385-4

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