Similar regional-scale survival of tropical and southern temperate birds from the New World.

Latitudinal gradient Life history Mortality Population dynamic South America

Journal

Oecologia
ISSN: 1432-1939
Titre abrégé: Oecologia
Pays: Germany
ID NLM: 0150372

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 19 10 2022
accepted: 05 05 2023
medline: 30 6 2023
pubmed: 31 5 2023
entrez: 30 5 2023
Statut: ppublish

Résumé

The general assumption that the survival patterns of tropical and southern temperate birds are similar lacks empirical data from higher latitudes. Regional comparisons of New World species are rare, and this assumption has been based on data from African studies. Here, we estimate the survival rates of 88 tropical and southern temperate bird populations (69 species) from eight localities in South America to evaluate the hypothesis that the survival of these populations is homogeneous at the regional scale. We estimated survival based on the Cormack-Jolly-Seber model and compared values from different environments. The survival estimates ranged from 0.30 to 0.80 (0.56 ± 0.12). Apparent survival did not differ significantly between low-latitude tropical environments (03°S) and the other sites from high-latitudes (between 22° and 34°S). Despite a predicted positive trend, body size was not significantly related to survival among passerines. On the other hand, phylogenetic relationships explained more than a third of the variation in bird survival. Based on the largest available database on South American bird species, our findings support the hypothesis that bird survival is homogeneous, at the regional scale, along the southern hemisphere. In particular, we reinforce the hypothesis that climatic variation has a limited influence on bird survival in the southern hemisphere.

Identifiants

pubmed: 37253787
doi: 10.1007/s00442-023-05381-2
pii: 10.1007/s00442-023-05381-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

239-250

Subventions

Organisme : Agencia Nacional de Promoción Científica y Tecnológica
ID : PIP-6411
Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
ID : PQ 306.579/2018-9
Organisme : Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
ID : E-26/202.835/2018

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

Ashmole NP (1963) The regulation of numbers of tropical oceanic birds. Ibis 103:458–473. https://doi.org/10.1111/j.1474-919X.1963.tb06766.x
doi: 10.1111/j.1474-919X.1963.tb06766.x
Auer SK, Bassar RD, Fontaine JJ, Martin TE (2007) Breeding biology of passerines in a subtropical montane forest in northwestern Argentina. Condor 109:321–333. https://doi.org/10.1093/condor/109.2.321
doi: 10.1093/condor/109.2.321
Barry SC, Brooks SP, Catchpole EA, Morgan BJT (2003) The analysis of ring-recovery data using random effects. Biometrics 59:54–65. https://doi.org/10.1111/1541-0420.00007
doi: 10.1111/1541-0420.00007 pubmed: 12762441
Bennett PM, Owens IPF (2002) Evolutionary ecology of birds—life histories, mating systems and extinction, 1st edn. Oxford University Press, Oxford
Billerman SM, Keeney BK, Rodewald PG, Schulenberg TS (2020) Birds of the World. Cornell Laboratory of Ornithology, Ithaca. https://birdsoftheworld.org/bow/home . Accessed 19 Aug 2022
Boyce AJ, Mouton JC, Lloyd P, Wolf BO, Martin TE (2020) Metabolic rate is negatively linked to adult survival but does not explain latitudinal differences in songbirds. Ecol Lett 23:642–652. https://doi.org/10.1111/ele.13464
doi: 10.1111/ele.13464 pubmed: 31990148
Bulit F, Massoni V (2011) Apparent survival and return rate of breeders in the southern temperate White-rumped Swallow Tachycineta leucorrhoa. Ibis 153:190–194. https://doi.org/10.1111/j.1474-919X.2010.01079.x
doi: 10.1111/j.1474-919X.2010.01079.x
Duca C, Marini MÂ (2014) High survival and low fecundity of a Neotropical savanna tanager. Emu 114:121–128. https://doi.org/10.1071/MU12036
doi: 10.1071/MU12036
França LF, Marini MÂ (2010) Negative population trend for Chapada flycatchers (Suiriri islerorum) despite high apparent annual survival. J Field Ornithol 81:227–236. https://doi.org/10.1111/j.1557-9263.2010.00279.x
doi: 10.1111/j.1557-9263.2010.00279.x
França LF, Silva CM, Paiva LV (2016) Effects of intrinsic and time-specific factors on daily nest survival of birds in a semiarid area of South America (Caatinga). Braz J Ornitol 24:228–234
doi: 10.1007/BF03544351
Gelman A (1996) Inference and monitoring convergence. In: Gilks WR, Richardson S, Spiegelhalter DJ (eds) Markov Chain Monte Carlo in practice. Chapman and Hall/CRC, Boca Raton, pp 131–143
Ghalambor CK, Martin TE (2001) Fecundity–survival trade-offs and parental risk-taking in birds. Science 292:494–497. https://doi.org/10.1126/science.1059379
doi: 10.1126/science.1059379 pubmed: 11313493
Guillerme T, Healy K (2014) mulTree: a package for running MCMCglmm analysis on multiple trees. R package. https://doi.org/10.5281/zenodo.12902
Hackett SJ, Kimball RT, Reddy S, Bowie RCK, Braun EL, Braun MJ, Chojnowski JL, Cox WA, Han KL, Harshman J, Huddleston CJ, Marks BD, Miglia KJ, Moore WS, Sheldon FH, Steadman DW, Witt CC, Yuri T (2008) A phylogenomic study of birds reveals their evolutionary history. Science 320:1763–1768. https://doi.org/10.1126/science.115770
doi: 10.1126/science.115770 pubmed: 18583609
Hadfield JD (2010) MCMC methods for multi-response generalized linear mixed models: the MCMCglmm R package. J Stat Softw 33:1–22. https://doi.org/10.18637/jss.v033.i02
doi: 10.18637/jss.v033.i02
Hadfield JD (2012). MCMCglmm course notes. http://stat.ethz.ch/CRAN/web/packages/MCMCglmm/index.html . Accessed 18 Aug 2022
Jansen DYM, Abadi F, Harebottle D, Altwegg R (2014) Does seasonality drive spatial patterns in demography? Variation in survival in African reed warblers Acrocephalus baeticatus across southern Africa does not reflect global patterns. Ecol Evol 4:889–898. https://doi.org/10.1002/ece3.958
doi: 10.1002/ece3.958 pubmed: 24772268 pmcid: 3997307
Jetz W, Thomas GH, Joy JB, Hartmann K, Mooers AO (2012) The global diversity of birds in space and time. Nature 491:7424. https://doi.org/10.1038/nature11631
doi: 10.1038/nature11631
Lack D (1947) The significance of clutch-size. Ibis 89:302–352
doi: 10.1111/j.1474-919X.1947.tb04155.x
Lebreton JD, Burnham KP, Clobert J, Anderson DR (1992) Modelling survival and testing biological hypotheses using marked animals: a unified approach with case studies. Ecol Monogr 62:67–118. https://doi.org/10.2307/2937171
doi: 10.2307/2937171
Lloyd P (2008) Adult survival, dispersal and mate fidelity in the white fronted Plover Charadrius marginatus. Ibis 150:182–187. https://doi.org/10.1111/j.1474-919X.2007.00739.x
doi: 10.1111/j.1474-919X.2007.00739.x
Lloyd P, Martin TE (2016) Fledgling survival increases with development time and adult survival across north and south temperate zones. Ibis 158:135–143. https://doi.org/10.1111/ibi.12325
doi: 10.1111/ibi.12325
Lloyd P, Abadi F, Altwegg R, Martin TE (2014) South temperate birds have higher apparent adult survival than tropical birds in Africa. J Avian Biol 45:493–500. https://doi.org/10.1111/jav.00454
doi: 10.1111/jav.00454
Martin TE (2002) A new view for avian life history evolution tested on an incubation paradox. P Roy Soc Lond B Bio 269:309–316. https://doi.org/10.1098/rspb.2001.1879
doi: 10.1098/rspb.2001.1879
Martin TE (2004) Avian life-history evolution has an eminent past: does it have a bright future? Auk 121:289–301. https://doi.org/10.1093/auk/121.2.289
doi: 10.1093/auk/121.2.289
Martin TE (2014) A conceptual framework for clutch-size evolution in songbirds. Am Nat 183:313–324. https://doi.org/10.1086/674966
doi: 10.1086/674966 pubmed: 24561596
Muñoz AP, Kéry M, Martins PV, Ferraz G (2018) Age effects on survival of Amazon forest birds and the latitudinal gradient in bird survival. Auk 135:299–313. https://doi.org/10.1642/AUK-17-91.1
doi: 10.1642/AUK-17-91.1
Nakagawa S, Schielzeth H (2013) A general and simple method for obtaining R
doi: 10.1111/j.2041-210x.2012.00261.x
Peach WJ, Hanmer DB, Oatley TB (2001) Do southern African songbirds live longer than their European counterparts? Oikos 93:235–249. https://doi.org/10.1034/j.1600-0706.2001.930207.x
doi: 10.1034/j.1600-0706.2001.930207.x
Pradel R, Hines JE, Lebreton JD, Nichols JD (1997) Capture-recapture survival models taking account of transients. Biometrics 53:60–72. https://doi.org/10.2307/2533097
doi: 10.2307/2533097
Presti PM, Amico GC, Bravo SP, Cueto VR (2018) Demography of the Neotropical austral migrant Elaenia albiceps chilensis (Tyrannidae) on its breeding grounds: climate and food offer effects. Braz J Ornithol 26:240–250. https://doi.org/10.1007/BF03544438
doi: 10.1007/BF03544438
Raftery AE, Lewis SM (1996) Implementing MCMC. In: Gilks WR, Richardson S, Spiegelhalter DJ (eds) Markov Chain Monte Carlo in Practice. Chapman and Hall/CRC, Boca Raton, pp 115–130
Ricklefs RE (1997) Comparative demography of New World populations of thrushes (Turdus spp.). Ecol Monogr 67:23–43. https://doi.org/10.1890/0012-9615(1997)067[0023:CDONWP]2.0.CO;2
doi: 10.1890/0012-9615(1997)067[0023:CDONWP]2.0.CO;2
Ricklefs RE (2000) Density dependence, evolutionary optimization, and the diversification of avian life histories. Condor 109:9–22. https://doi.org/10.1093/condor/102.1.9
doi: 10.1093/condor/102.1.9
Ricklefs RE, Wikelski M (2002) The physiology/life history nexus. Trends Ecol Evol 17:462–468. https://doi.org/10.1016/S0169-5347(02)02578-8
doi: 10.1016/S0169-5347(02)02578-8
Ricklefs RE, Tsunekage T, Shea RE (2011) Annual adult survival in several New World passerine birds based on age ratios in museum collections. J Onithol 152:481–495. https://doi.org/10.1007/s10336-010-0614-9
doi: 10.1007/s10336-010-0614-9
Robinson WD, Hau M, Klasing KC, Wikelski M, Brawn JD, Austin SH, Tarwater CE, Ricklefs RE (2010) Diversification of life histories in New World birds. Auk 127:253–262. https://doi.org/10.1525/auk.2010.127.2.253
doi: 10.1525/auk.2010.127.2.253
Roff DA (1992) The evolution of life histories, 1st edn. Chapman and Hall, New York
Roff DA (2002) Life history evolution, 1st edn. Sinauer Associats, Oxford
Rowley I, Russel E (1991) Demography of passerines in the temperate southern hemisphere. In: Perrins CM, Lebreton JD, Hirons GJM (eds) Bird population studies: relevance to conservation and management. Oxford University Press, New York, pp 22–44
Sæther BE (1988) Pattern of covariation between life-history traits of European birds. Nature 331:616–617. https://doi.org/10.1038/331616a0
doi: 10.1038/331616a0 pubmed: 3340211
Sæther BE (1989) Survival rates in relation to body weight in European birds. Ornis Scand 20:13–21. https://doi.org/10.2307/3676702
doi: 10.2307/3676702
Sandercock BK (2006) Estimation of demographic parameters from live-encounter data: a summary review. J Wildlife Manage 70:1504–1520. https://doi.org/10.2193/0022-541X(2006)70[1504:EODPFL]2.0.CO;2
doi: 10.2193/0022-541X(2006)70[1504:EODPFL]2.0.CO;2
Sandercock BK, Beissinger SR, Stoleson SH, Melland RR, Hughes CR (2000) Survival rates of a Neotropical parrot: implications for latitudinal comparisons of avian demography. Ecology 81:1351–1370. https://doi.org/10.1890/0012-9658(2000)081[1351:SROANP]2.0.CO;2
doi: 10.1890/0012-9658(2000)081[1351:SROANP]2.0.CO;2
Schloss AL, Kicklighter DW, Kaduk J, Wittenberg U (1999) Comparing global models of terrestrial net primary productivity (NPP): comparison of NPP to climate and the normalized difference vegetation index (NDVI). Glob Change Biol 5:25–34. https://doi.org/10.1046/j.1365-2486.1999.00004.x
doi: 10.1046/j.1365-2486.1999.00004.x
Scholer MN, Strimas-Mackey M, Jankowski JE (2020) A meta-analysis of global avian survival across species and latitude. Ecol Lett 23:1537–1549. https://doi.org/10.1111/ele.13573
doi: 10.1111/ele.13573 pubmed: 32696563
Skutch AF (1949) Do tropical birds rear the many young the they can nourish? Ibis 91:430–455. https://doi.org/10.1111/j.1474-919X.1949.tb02293.x
doi: 10.1111/j.1474-919X.1949.tb02293.x
Speakman JR (2005) Body size, energy metabolism and lifespan. J Exp Biol 208:1717–1730. https://doi.org/10.1242/jeb.01556
doi: 10.1242/jeb.01556 pubmed: 15855403
Stutchbury BJM, Morton ES (2001) Behavioral ecology of tropical birds, 1st edn. Academic Press, California
Thomson RF, Estades CF (2012) Survival rates of forest passerines in south-central Chile. Ornitol Neotrop 23:1–9
Wiersma P, Munõz-García A, Walker A, Williams JB (2007) Tropical birds have a slow pace of life. P Natl Acad Sci USA 104:9340–9345. https://doi.org/10.1073/pnas.0702212104
doi: 10.1073/pnas.0702212104
Wikelski M, Spinney L, Schelsky W, Scheuerlein A, Gwinner E (2003) Slow pace of life in tropical sedentary birds: a common garden experiment on four stonechat populations from different latitudes. P R Soc London B Bio 270:2383–2388. https://doi.org/10.1098/rspb.2003.2500
doi: 10.1098/rspb.2003.2500
Williams BK, Nichols JD, Conroy M (2002) Analysis and management of animal populations, 1st edn. Academic Press, London, p 817

Auteurs

Leonardo Fernandes França (LF)

Laboratório de Ecologia de Populações Animais, Departamento de Biociências, Universidade Federal Rural do Semi-Árido, Mossoró, RN, 59625-900, Brazil. franca_lf@ufersa.edu.br.

Clarisse Caroline de Oliveira E Silva (CC)

Centro de Biociências, Pós-Graduação em Ecologia, Universidade Federal do Rio Grande do Norte, Natal, RN, Brazil.

João Batista de Pinho (JB)

Laboratório de Ornitologia, Instituto de Biologia, Universidade Federal de Mato Grosso, Cuiabá, MT, Brazil.

Nêmora Pauletti Prestes (NP)

Departamento de Vida Silvestre da Associação Amigos do Meio Ambiente, Carazinho, RS, Brazil.

Victor R Cueto (VR)

Laboratorio de Ecología de Aves, Centro de Investigación Esquel de Montaña Y Estepa Patagónica, Consejo Nacional de Investigaciones Científicas y Técnicas, Universidad Nacional de la Patagonia, San Juan Bosco, Esquel, Chubut, Argentina.

Maria Alice S Alves (MAS)

Departamento de Ecologia, Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.

Fabio Schunck (F)

Comitê Brasileiro de Registros Ornitológicos, São Paulo, SP, Brazil.

Carla Suertegaray Fontana (CS)

Centro de Ecologia, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.

Camile Lugarini (C)

Centro Nacional de Pesquisa e Conservação de Aves Silvestres, Instituto Chico Mendes, Florianópolis, SC, Brazil.

Jaime Martinez (J)

Instituto da Saúde, Universidade de Passo Fundo, Passo Fundo, RS, Brazil.

M Cecilia Sagario (MC)

Instituto de Investigaciones en Biodiversidad y Medioambiente, Centro de Ecología Aplicada de Neuquén, Universidad Nacional del Comahue, Junín de los Andes, Neuquén, Argentina.

Javier Lopez de Casenave (JL)

Departamento de Ecología, Facultad de Ciencias Exactas y Naturales, Genética y Evolución, Universidad de Buenos Aires and IEGEBA, Buenos Aires, Argentina.

Maurício B Vecchi (MB)

Departamento de Ecologia, Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.

Márcio Repenning (M)

Universidade Federal do Rio Grande, Rio Grande, RS, Brazil.

Ariane Ferreira (A)

Centro de Ciências Biológicas, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil.

Raphael Igor Dias (RI)

Faculdade de Ciências da Educação e Saúde, Centro Universitário de Brasília, Brasília, DF, Brazil.

Daniel Cunha Passos (DC)

Laboratório de Ecologia e Comportamento Animal, Programa de Pós-Graduação em Ecologia e Conservação, Departamento de Biociências, Centro de Ciências Biológicas e da Saúde, Universidade Federal Rural do Semi-Árido, Mossoró, RN, Brazil.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing
Animals Hemiptera Insect Proteins Phylogeny Insecticides
Amaryllidaceae Alkaloids Lycoris NADPH-Ferrihemoprotein Reductase Gene Expression Regulation, Plant Plant Proteins
Drought Resistance Gene Expression Profiling Gene Expression Regulation, Plant Gossypium Multigene Family

Classifications MeSH