Hostname: page-component-78c5997874-s2hrs Total loading time: 0 Render date: 2024-11-10T19:28:03.840Z Has data issue: false hasContentIssue false

Avifauna and biogeographical affinities of a carrasco-dominated landscape in north-eastern Brazil: providing baseline data for future monitoring

Published online by Cambridge University Press:  15 April 2021

HEVANA SANTANA DE LIMA*
Affiliation:
Laboratório de Ecologia & Evoluçao de Aves, Departamento de Zoologia, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil. Programa de Pós-Graduação em Biologia Animal UFPE, Universidade Federal de Pernambuco, Av. Prof. Nelson Chaves, s/n - Cidade Universitária, Recife, Pernambuco, Brazil.
FLOR MARIA GUEDES LAS-CASAS
Affiliation:
Laboratório de Ecologia & Evoluçao de Aves, Departamento de Zoologia, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil. Ciências Biológicas, Centro de Estudos Superiores de Zé Doca, Universidade Estadual do Maranhão, Rua Rio Branco, s/n – Centro, Zé Doca, Maranhão, Brazil.
JONATHAN RAMOS RIBEIRO
Affiliation:
Laboratório de Ecologia & Evoluçao de Aves, Departamento de Zoologia, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil.
WEBER ANDRADE GIRÃO
Affiliation:
AQUASIS, Associação de Pesquisa e Preservação de Ecossistemas Aquáticos, Caucaia, Ceará, Brazil.
DANIELE MARIZ
Affiliation:
Laboratório de Ecologia & Evoluçao de Aves, Departamento de Zoologia, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil.
LUCIANO N. NAKA
Affiliation:
Laboratório de Ecologia & Evoluçao de Aves, Departamento de Zoologia, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil.
*
*Author for correspondence; e-mail: hevana.lima@ufpe.br

Summary

The carrasco is a dense, shrubby vegetation type that covers the higher parts of table-top mountains in north-eastern Brazil. The vegetation of this phytophysiognomy is often considered to have biogeographical and ecological affinities with the cerrado of Central Brazil, but the biogeographical affinities of its avifauna remain unclear. In recent years, deforestation due to local economic activities has been particularly severe in some carrasco-dominated landscapes. In 2013, we initiated avian surveys at the Fazenda Pau D‘Arco, a privately owned property located on top of the Araripe Plateau, to evaluate the effects of a legal forest management program on the avifauna. Here, we present the results of four years of avian inventories to: i) characterize a well-preserved patch of carrasco vegetation; ii) assess avian biogeographical affinities of this vegetation type; iii) identify associations between managed/unmanaged areas and bird species; and iv) provide baseline data for future avian monitoring studies. Using different survey methods, we provide a list of 148 bird species, including several dry-forest specialists and caatinga endemics. Biogeographically, the avifauna of the carrasco represents a subsample of the Caatinga dry forest, lacking cerrado elements. Forest management significantly affected the distribution of several bird species in the study area. We found that 1/5 of the species (24) recorded during our standardized surveys were significantly associated with either unmanaged (14 species) or managed (10 species) areas. Species such as the Ceará Leaftosser Sclerurus cearensis, a globally vulnerable species, have only been detected in non-managed areas and therefore can be negatively affected by the management program. We also present data on 16 avian taxa with ecological and conservation concerns. By presenting a fairly complete and documented list of the avifauna, we characterize the carrasco avifauna and offer the tools to evaluate the effects of forest management on this poorly known vegetation type.

Type
Research Article
Copyright
© The Author(s), 2021. Published by Cambridge University Press on behalf of BirdLife International

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Alves, R. J. and Kolbek, J. (2010) Can campo rupestre vegetation be floristically delimited based on vascular plant genera? Plant Ecol. 207: 6779.CrossRefGoogle Scholar
Anderson, M. J. (2001) A new method for non-parametric multivariate analysis of varianceAustral Ecol26: 3246.Google Scholar
Araújo, F. S., Martins, F. R. and Shepherd, G. J. (1999) Variações estruturais e florísticas do carrasco no planalto da Ibiapaba, estado do Ceará. Rev. Bras. Biol. 59: 663678.CrossRefGoogle Scholar
Araújo, F. S., Sampaio, E. V. S. B., Figueiredo, M. A., Rodal, M. J. N. and Fernandes, A. G. (1998) Composição florística da vegetação de carrasco, Novo Oriente, CE. Rev. Bras. Bot. 21: 105116.CrossRefGoogle Scholar
Araújo, H. F. P. and da Silva, J. M. C. (2017) The avifauna of the Caatinga: biogeography, ecology, and conservation. Pp. 181210. In Caatinga: The largest tropical dry forest region in South America. Springer International Publishing. https://doi.org/10.1007/978-3-319-68339-3_7.CrossRefGoogle Scholar
Billerman, S. M., Keeney, B. K., Rodewald, P. G. and Schulenberg, T. S. (Eds). (2020) Birds of the world. Ithaca, NY, USA: Cornell Laboratory of Ornithology. https://birdsoftheworld.org/bow/home.CrossRefGoogle Scholar
Brewer, D. (2020) Green-winged Saltator (Saltator similis), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A. and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.grwsal1.01.Google Scholar
Cáceres, M. D. and Legendre, P. (2009) Associations between species and groups of sites: indices and statistical inferenceEcology 90: 35663574.CrossRefGoogle ScholarPubMed
Castelletti, C. H. M., Silva, J. M. C. D., Tabarelli, M. and Santos, A. M. M. (2003) Quanto ainda resta da Caatinga? Uma estimativa preliminar, Pp. 91100 in Biodiversidade da Caatinga: áreas e ações prioritárias para a conservação. Brasília: Ministério do Meio Ambiente.Google Scholar
Chaves, E. M. F., and Barros, R. F. M. (2008) Resource use of the flora of the brushwonod vegetation in Cocal Country, Piauí, Brazil. Func. Ecos. and Commu. 2: 5158.Google Scholar
Collar, N. J. (2000) Opinion. Collecting and conservation: cause and effect. Bird Conserv. Internatn. 10: 115.CrossRefGoogle Scholar
Cracraft, J. (1985) Historical biogeography and patterns of differentiation within the South American avifauna: areas of endemism. Ornitol. Monogr. 36: 4984.CrossRefGoogle Scholar
d’Horta, F. M., Cuervo, A. M., Ribas, C. C., Brumfield, R. T. and Miyaki, C. Y. (2013) Phylogeny and comparative phylogeography of Sclerurus (Aves: Furnariidae) reveal constant and cryptic diversification in an old radiation of rain forest understorey specialistsJ. Biogr. 40: 3749.CrossRefGoogle Scholar
del Hoyo, J. and Kirwan, G. M. (2020) Rusty-margined Guan (Penelope superciliaris). Version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A. and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.rumgua1.01.Google Scholar
del Hoyo, J., Remsen, J. V., Kirwan, G. M. and Collar, N. (2020) Rufous-breasted Leaftosser (Sclerurus scansor), version 1.0. In Billerman, S. M. Keeney, B. K. Rodewald, P. G., and Schulenberg, T. S., eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.rublea1.01.Google Scholar
Dufrêne, M. and Legendre, P. (1997) Species assemblages and indicator species: the need for a flexible asymmetrical approachEcol. Monogr67: 345366.Google Scholar
Farias, G. B., Girão e Silva, W. A. and Albano, C. G. (2006) Diversidade de aves em áreas prioritárias para conservação de aves da Caatinga. Pp 204-226 in Análise das variações da biodiversidade do bioma caatinga. Suporte a estratégias regionais de conservação. Brasília: Ministério do Meio Ambiente.Google Scholar
Figueiredo, M. A. (1986) Vegetação. Pp. 2425 in Atlas do Ceará. Fortaleza: SUDEC.Google Scholar
Fitzpatrick, J. W. (2020) Greater Wagtail-Tyrant (Stigmatura budytoides), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A. and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.grwtyr1.01.Google Scholar
Fitzpatrick, J. W., del Hoyo, J., Kirwan, G. M. and Collar, N. (2020) Lesser Wagtail-Tyrant (Stigmatura napensis), version 1.0. In Billerman, S. M. Keeney, B. K. Rodewald, P. G., and Schulenberg, T. S., eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.lewtyr1.01.Google Scholar
Giulietti, A. M., Bocage Neta, A. L., Castro, A. A. J. F., Gamarra-Rojas, C. F. L., Sampaio, E. V. S. B., Virgínio, J. F., Queiroz, L. P., Figueiredo, M. A., Rodal, M. J. N., Barbosa., M. R. V. and Harley, R. M. (2004) Diagnóstico da vegetação nativa do bioma Caatinga. Biodiversidade da Caatinga: áreas e ações prioritárias para a conservação. https://ainfo.cnptia.embrapa.br.Google Scholar
Gower, J. C. (1966) Some distance properties of latent rOt and vector methods used in multivariate analysisBiometrika 53: 325328.CrossRefGoogle Scholar
Greeney, H. F. (2020) White-browed Antpitta (Hylopezus ochroleucus), version 1.0. In Schulenberg, T. S., ed. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.whbant7.01.Google Scholar
Haffer, J. (1985) Avian zoogeography of the Neotropical lowlands. Ornith. Monogr. 36: 113146.CrossRefGoogle Scholar
IUCN (2020) Red List of Threatened Species. Available at: http://www.iucnredlist.orgGoogle Scholar
Koloff, J. and Mennill, D. J. (2020) Barred Antshrike (Thamnophilus doliatus), version 1.0. In Schulenberg, T. S., ed. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.barant1.01.Google Scholar
Lima, H. S., Las-Casas, F. M. G., Ribeiro, J. R., Gonçalves-Souza, T. and Naka, L. N. (2018) Ecological and phylogenetic predictors of mobbing behavior in a tropical dry forestEcol. Evol. 8: 1261512628.Google Scholar
Lima, R. D., Tomotani, B. M. and Silveira, L. F. (2020) Colour variation and taxonomy of Picumnus limae Snethlage, 1924 and P. fulvescens Stager, 1961 (Piciformes: Picidae). J. Ornithol. 2020: 1:11.Google Scholar
Machado, C. G., de Araújo, H. F. P., Alves, R. R. N. and Mendes, D. (2018) Plano de ação nacional para a conservação das aves da Caatinga. Brasília: Instituto Chico Mendes de Conservação da Biodiversidade, ICMBio.Google Scholar
Mazar Barnett, J., Ingels, J., Ros, A. L. and Naka, L. N. (2014) Observations on the breeding biology of the Pygmy Nightjar Hydropsalis hirundinacea in the Caatinga of Bahia, Brazil. Rev. Bras. Ornitol. 22: 201209.CrossRefGoogle Scholar
MMA (2018) Livro Vermelho da Fauna Brasileira Ameaçada de Extinção. Brasília, DF: ICMBio/ Ministério do Meio Ambiente.Google Scholar
Nascimento, J. L. X., Nascimento, I. D. L. S. and de Azevedo Júnior, S. M. (2000) Aves da Chapada do Araripe (Brasil): biologia e conservação. Floresta 1: 6.Google Scholar
Pacheco, J. F. (2004) As aves da Caatinga: uma análise histórica do conhecimento. Pp. 189250 in Silva, J. M. C. Tabarelli, M. Fonseca, M. T. and Lins, L. V., eds. Biodiversidade da Caatinga: áreas e ações prioritárias para a conservação. Brasília: Ministério do Meio Ambiente, Universidade Federal de Pernambuco.Google Scholar
Pavey, C. R., and Nano, C. E. M. (2009) Bird assemblages of arid Australia: vegetation patterns have a greater effect than disturbance and resource pulsesJ. Arid Environ73: 634642.CrossRefGoogle Scholar
Pennington, R. T., Lavin, M. and Oliveira-Filho, A. (2009) Woody plant diversity, evolution, and ecology in the tropics: perspectives from seasonally dry tropical forests. Annu. Rev. Ecol. Evol. Systemat. 40: 437457.CrossRefGoogle Scholar
Piacentini, V. D. Q., Aleixo, A., Agne, C. E., Maurício, G. N., Pacheco, J. F., Bravo, G. A., Brito, G. R., Naka, L. N., Olmos, F., Posso, S. and Silveira, L. F. (2015) Annotated checklist of the birds of Brazil by the Brazilian Ornithological Records Committee / Lista comentada das aves do Brasil pelo Comitê Brasileiro de Registros OrnitológicosRev. Bras. Ornitol. 23: 90298.CrossRefGoogle Scholar
Queiroz, L. P., Cardoso, D., Fernandes, M. F. and Moro, M. F. (2017Diversity and evolution of flowering plants of the caatinga domain. Caatinga 2017: 2363.CrossRefGoogle Scholar
R Core Team (2020) R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing. Available at: https://www.R-project.org/.Google Scholar
Remsen, J. V. (2020a) Great Xenops (Megaxenops parnaguae), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A., and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.grexen1.01.Google Scholar
Remsen, J. V. (2020b) Red-shouldered Spinetail (Synallaxis hellmayri), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A., and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.resspi2.01.Google Scholar
Remsen, J. V. (2020c) Ochre-cheeked Spinetail (Synallaxis scutata), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A., and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.occspi1.01.Google Scholar
Ribeiro, J. R., Las-Casas, F. M. G., Silva, W. A. G. and Naka, L. N. in Press a. Managed logging negatively affects the density and abundance of some dry forest specialist bird species of northeastern Brazil. Ornithological Applications.Google Scholar
Ribeiro, J. R., Las-Casas, F. M. G., Lima, H. S., Silva, W. A. G. and Naka, L. N. in Press b. The effect of forest management on the avifauna of a Brazilian Dry Forest. Frontiers in Ecology and Evolution.Google Scholar
Santos, M. P. D., Santana, A., Soares, L. M. S. and Sousa, S. A. (2012) Avifauna of Serra Vermelha, Southern Piauí, Brazil. Rev. Brasil. Ornitol. 20: 199214.Google Scholar
Schunck, F., Piacentini, V. D., de Souza, E. A., de Sousa, A. E., Rego, M. A., Albano, C., Nunes, M. F., de Lima Favaro, F., Neto, I. S., Mariano, E. F. and Lima, D. M. (2012) Birds of the Lower Middle São Francisco River. Rev. Brasil. Ornitol. 20: 350364.Google Scholar
Sekercioglu, C. H. (2006) Increasing awareness of avian ecological function. Trends Ecol. Evol. 21: 464471.CrossRefGoogle ScholarPubMed
Shahabuddin, G. and Kumar, R. (2006) Influence of anthropogenic disturbance on bird communities in a tropical dry Forest: role of vegetation structure. Anim. Conserv. 9: 404413.CrossRefGoogle Scholar
Smouse, P. E., Long, J. C. and Sokal, R. R. (1986) Multiple regression and correlation extensions of the Mantel test of matrix correspondenceSyst. Zool35: 627632.CrossRefGoogle Scholar
Sneath, P. H. A. (1957) Some thoughts on bacterial classification. J. Gen. Micro. 184–200CrossRefGoogle Scholar
Sousa, A. E. B. A., Lima, D. M. and Lyra-Neves, R. M. (2012) Avifauna of the Catimbau national park in the Brazilian state of Pernambuco, brazil: species richness and spatio-temporal variation. Rev. Brasil. Ornitol. 20: 16.Google Scholar
Stotz, D. F., Fitzpatrick, J. W., Parker, T. A. III and Moskovits, D. K. (1996Neotropical birds: ecology and conservation. Chicago, IL: University of Chicago Press.Google Scholar
Stouffer, P. C. (2020). Birds in fragmented Amazonian rainforest: Lessons from 40 years at the Biological Dynamics of Forest Fragments ProjectCondor 122: 115.CrossRefGoogle Scholar
Tomotani, B. M. and Silveira, L. F. (2016) A reassessment of the taxonomy of Crypturellus noctivagus (Wied, 1820). Rev. Bras. Ornitol. 24: 3445.CrossRefGoogle Scholar
Vasconcelos, M. F., Souza, L. N., Duca, C., Pacheco, J. F., Parrini, R., Serpa, G. A., Albano, C., Abreu, C. R. M., dos Santos, S. S. and Neto, F. P. F. (2012) The avifauna of Brejinho das Ametistas, Bahia, Brazil: birds in a caatinga-cerrado transitional zone, with comments on taxonomy and biogeography. Rev. Bras. Ornitol. 20: 22.Google Scholar
Vasconcelos, S. F., de Araújo, F. S. and Lopes, A. V. (2010) Phenology and dispersal modes of wood species in the Carrasco, a tropical deciduous shrubland in the Brazilian semiarid. Biodivers Conserv. 19: 22632289.CrossRefGoogle Scholar
Venter, O., Sanderson, E. W., Magrach, A, Allan, J. R., Beher, J, Jones, K. R., Possingham, H. P., Laurance, W., Wood, P., Fekete, B. M., Levy, M. A. and Watson, J. E. M. (2016) Sixteen years of change in the global terrestrial human footprint and implications for biodiversity conservation. Nat. Comm. 7: 111.CrossRefGoogle ScholarPubMed
Wiens, J. A. (1994) Habitat fragmentation: island v. landscape perspectives on bird conservation. Ibis 137: 97104.CrossRefGoogle Scholar
Winkler, H., Christie, D. A. and Bonan, A. (2020a) Spotted Piculet (Picumnus pygmaeus), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A., and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.spopic1.01Google Scholar
Winkler, H., Christie, D. A. and de Juana, E. (2020b) Ochraceous Piculet (Picumnus limae), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A., and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.ochpic1.01Google Scholar
Zimmer, K. and Isler, M. L. (2020a) Caatinga Antwren (Herpsilochmus sellowi), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A., and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.caaant1.01Google Scholar
Zimmer, K. and Isler, M. L. (2020b) Silvery-cheeked Antshrike (Sakesphorus cristatus), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A., and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.sicant1.01Google Scholar
Zimmer, K., Isler, M. L. and Kirwan, G. M. (2020) Stripe-backed Antbird (Myrmorchilus strigilatus), version 1.0. In Hoyo, J. del Elliott, A. Sargatal, J. Christie, D. A., and Juana, E. de, eds. Birds of the world. Ithaca, NY, USA: Cornell Lab of Ornithology. Available at: https://doi.org/10.2173/bow.stbant2.01Google Scholar
Zwarts, L., Bijlsma, R. G. and van der Kamp, J. (2018) Large decline of birds in Sahelian rangelands due to loss of woody cover and soil seed bankJ. Arid Environ 155: 115.CrossRefGoogle Scholar
Supplementary material: File

De Lima et al. supplementary material

De Lima et al. supplementary material 1

Download De Lima et al. supplementary material(File)
File 56.2 KB
Supplementary material: File

De Lima et al. supplementary material

De Lima et al. supplementary material 2

Download De Lima et al. supplementary material(File)
File 94.3 KB