PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2013 | 15 | 2 |

Tytuł artykułu

High dispersal and generalist habits of the bat Artibeus jamaicensis on Cozumel Island, Mexico: an assessment using molecular genetics

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Islands and insular biotas have been recognized as ideal models for studying adaptive radiations and evolutionary processes. In the present study we investigated the Jamaican fruit-eating bat, Artibeus jamaicensis from Cozumel Island, to evaluate the effect of ecological features on genetic diversity and structure across three different environments, semi-evergreen tropical forest, mangrove, and cenotes, using six microsatellite loci in 105 individuals. Genetic diversity was relatively high (forest HO = 0.693, HNei = 0.825; mangrove HO = 0.702, HNei = 0.710; cenotes HO = 0.695, HNei = 0.847). Pairwise genetic differentiation measures between localities were not significant and the overall level of differentiation was markedly low (FST = 0.009, G'ST = 0.088). Likewise, results showed that A. jamaicensis consists of one genetic group and relatedness among individuals was low. Results are concordant with our predictions that the island population will show high genetic diversity and null structure at the fine spatial scale examined. We conclude that ecological features like dispersal and generalist habits are the factors influencing population structure and genetic diversity of A. jamaicensis on the island, and that factors like the species polygynous mating system, female philopatry and male differential dispersal do not prevail in the island population. Cozumel Island is facing severe conservation problems, mainly from habitat perturbation, urbanization and introduction of exotic species, hence the present genetic information is of great value as a basis for future research and protection of the species.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

15

Numer

2

Opis fizyczny

p.411-421,fig.,ref.

Twórcy

  • Departamento de Ecologia de la Biodiversidad, Instituto de Ecologia, Universidad Nacional Autonoma de Mexico, Ap. Postal 70-275, Ciudad Universitaria, Mexico DF 04510, Mexico
  • Departamento de Ecologia de la Biodiversidad, Instituto de Ecologia, Universidad Nacional Autonoma de Mexico, Ap. Postal 70-275, Ciudad Universitaria, Mexico DF 04510, Mexico
  • Centro de Investigacion de Biodiversidad y Conservacion, Universidad Autonoma del Estado de Morelos, Av. Universidad 1001, Col. Chamilpa, Cuernavaca, Morelos 62209, Mexico
autor
  • SACBE - Servicios Ambientales, Conservacion Biologica y Educacion, Pelicanos 75, Colonia Flamingos II, Cozumel, Quintana Roo 77660, Mexico
  • Multicriteria SC, Torre Uxmal 18, Unidad Independencia IMSS, Mexico DF 10100, Mexico

Bibliografia

  • 1. J. Abdelkrim , M. Pascal , and S. Samadi . 2005. Island colonization and founder effects: the invasion of the Guadeloupe islands by ship rats (Rattus rattus). Molecular Ecology, 14: 2923–2931. Google Scholar
  • 2. F. W. Allendorf , and G. Luikart . 2007. Conservation and the genetics of populations. Wiley-Blackwell Publishing Ltd, Maiden, MA, 642 pp. Google Scholar
  • 3. J. H. Brown , and A. C. Gibson . 1983. Biogeography. C.V. Mosby Co., St. Louis, MO, 643 pp. Google Scholar
  • 4. J. H. Brown , and M. V. Lomolino . 1998. Biogeography, 2nd edition. Sinauer Associates, Inc., Sunderland, MA, 691 pp. Google Scholar
  • 5. T. M. Burland , and J. Worthington Wilmer . 2001. Seeing in the dark: molecular approaches to the study of bat populations. Biological Review, 76: 389–409. Google Scholar
  • 6. T. M. Burland , E. M. Barratt , M. A. Beaumont , and P. A. Racey . 1999. Population genetic structure and gene flow in a gleaning bat, Plecotus auritus. Proceedings of the Royal Society of London, 266B: 975–980. Google Scholar
  • 7. B. C. Carstens , J. Sullivan , L. M. Davalos , P. A. Larsen , and S. C. Pedersen . 2004. Exploring population genetic structure in three species of Lesser Antillean bats. Molecular Ecology, 13: 2557–2566. Google Scholar
  • 8. M. Chapuis , and P. A. Estoup . 2007. Microsatellite null alleles and estimation of population differentiation. Molecular Biology and Evolution, 24: 621–631. Google Scholar
  • 9. A. D. Cuarón 2009. Cozumel. Pp. 203–206, in Encyclopedia of islands ( R. G. Gillespie and D. A. Clague , eds.). University of California Press, Berkeley, CA, 1008 pp. Google Scholar
  • 10. A. D. Cuarón , D. Valenzuela-Galván , D. García-Vasco , M. E. Copa , S. Bautista , H. Mena , D. Martínez-Godínez , C. González-Baca , L. A. Bojórquez-Tapia , L. Barraza , et al. 2009. Conservation of the endemic dwarf carnivores of Cozumel Island, Mexico. Small Carnivores Conservation, 41: 15–21. Google Scholar
  • 11. A. D. Ditchfield 2000. The comparative phylogeography of Neotropical mammals: patterns of intraspecific mitochondrial DNA variation among bats contrasted to nonvolant small mammals. Molecular Ecology, 9: 1307–1318. Google Scholar
  • 12. M. D. Dixon 2011. Population genetic structure and natal philopatry in the widespread North American bat Myotis lucifugus. Journal of Mammalogy, 92: 1343–1351. Google Scholar
  • 13. M. D. B. Eldridge , J. M. King , A. K. Loupis , P. B. S. Spencer , A. C. Taylor , L. C. Pope , and G. P. Hall . 1999. Unprecedented low levels of genetic variation and inbreeding depression in an island population of the black-footed rockwallaby. Conservation Biology, 13: 531–541. Google Scholar
  • 14. M. D. B. Eldridge , J. E. Kinnear , K. R. Zenger , L. M. McKenzie , and P. B. S. Spencer . 2004. Genetic diversity in remnant mainland and ‘pristine’ island populations of three endemic Australian macropodids (Marsupialia): Macropus eugenii, Lagorchestes hirsutus and Petrogale lateralis. Conservation Genetics, 5: 325–338. Google Scholar
  • 15. L. Excoffier , P. E. Smouse , and J. M. Quattro . 1992. Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics, 131: 479–491. Google Scholar
  • 16. L. Excoffier , G. Laval , and S. Schneider . 2005. Arlequin (version 3.0): an integrated software package for population genetics data analysis. Evolutionary Bioinformatics Online, 1: 47–50. Google Scholar
  • 17. T. H. Fleming , and K. L. Murray . 2009. Population and genetic consequences of hurricanes for three species of West Indian phyllostomid bats. Biotropica, 41: 250–256. Google Scholar
  • 18. T. H. Fleming , K. L. Murray , and B. Carstens . 2010. Phylogeography and genetic structure of three evolutionary lineages of West Indian phyllostomid bats. Pp. 116–150, in Island bats. Evolution, ecology, and conservation ( T. H. Fleming and P. A. Racey , eds.). University of Chicago Press, Chicago, IL, 549 pp. Google Scholar
  • 19. R. Frankham 1997. Do island populations have less genetic variation than mainland populations? Heredity, 78: 311–327. Google Scholar
  • 20. R. Frankham 1998. Inbreeding and extinction: islands populations. Conservation Biology, 12: 665–675. Google Scholar
  • 21. R. Frankham , J. Ballou , and D. Briscoe . 2005. Introduction to conservation genetics. Cambridge University Press, Cambridge, UK, 618 pp. Google Scholar
  • 22. E. Fuentes-Montemayor , A. D. Cuarón , E. Vázquez-Domínguez , J. Benítez-Malvido , D. Valenzuela , and E. Andresen . 2009. Living on the edge: roads and edge effects on small mammal populations. Journal of Animal Ecology, 78: 857–865. Google Scholar
  • 23. P. Grant (ed.). 1998. Evolution on islands. Oxford University Press, Oxford, UK, 352 pp. Google Scholar
  • 24. G. Guillot 2009. On the inference of spatial structure from population genetics data. Bioinformatics, 25: 1796–1801. Google Scholar
  • 25. G. Guillot , F. Mortier , and A. Estoup . 2005. GENELAND: a computer package for landscape genetics. Molecular Ecology Notes, 5: 712–715. Google Scholar
  • 26. G. Guillot , R. Leblois , A. Coulon , and A. C. Frantz . 2009. Statistical methods in spatial genetics. Molecular Ecology, 18:4734–4756. Google Scholar
  • 27. G. Guillot , F. Santos , and A. Estoup . 2010. Population genetics analysis using R and Geneland. Technical University of Denmark. Available at: http://www2.imm.dtu.dk/∼gigu/Geneland/. Google Scholar
  • 28. S. W. Guo , and E. A. Thompson . 1992. Performing the exact test of Hardy-Weinberg proportion for multiple alleles. Biometrics, 4: 361–372. Google Scholar
  • 29. R. Heller , and H. R. Siegismund . 2009. Relationship of three measures of genetic differentiation GST, DEST, G'ST: how wrong have we been? Molecular Ecology, 18: 2080–2083. Google Scholar
  • 30. G. Hinten , F. Harris , M. Rossetto , and P. R. Baverstock . 2003. Genetic variation and island biogeography: microsatellite and mitochondrial DNA variation in island populations of the Australian bush rat, Rattus fuscipes greyii. Conservation Genetics, 4: 759–778. Google Scholar
  • 31. J. L. Jensen , A. J. Bohonak , and S. T. Kelley . 2005. Isolation by distance, web service. BMC Genetics, 6: 1–6. Google Scholar
  • 32. K. E. Jones , S. P. Mickleburgh , and A. L. Walsh . 2009. Global overview of the conservation of island bats: importance, challenges and opportunities. Pp. 496–530, in Island bats: evolution, ecology and conservation ( T. H. Fleming and P. A. Racey , eds.). University of Chicago Press, Chicago, IL, 549 pp. Google Scholar
  • 33. L. Jost 2008. GST and its relatives do not measure differentiation. Molecular Ecology, 17: 4015–4026. Google Scholar
  • 34. J. Juste , C. Ibáñez , and A. Machordom . 2000. Morphological and allozyme variation of Eidolon helvum (Mammalia: Megachiroptera) in the islands of the Gulf of Guinea. Biological Journal of the Linnean Society, 71: 359–378. Google Scholar
  • 35. J. C. Juste , R. Bilgin , J. Muñoz , and C. Ibáñez . 2009. Mitochondrial DNA signatures at different spatial scales: from the effects of the Straits of Gibraltar to population structure in the meridional serotine bat (Eptesicus isabellinus). Heredity, 103: 178–187. Google Scholar
  • 36. S. T. Kalinowski , A. P. Wagner , and M. L. Taper . 2006. ML-RELATE: a computer program for maximum likelihood estimation of relatedness and relationship. Molecular Ecology Notes, 6: 576–579. Google Scholar
  • 37. C. W. Kilpatrick 1981. Genetic structure of insular populations. Pp. 28–59, in Mammalian population genetics ( M. H. Smith and J. Joule , eds.). University of Georgia Press, Athens, GA, 380 pp. Google Scholar
  • 38. T. H. Kunz , E. B. Arnett , W. P. Erickson , A. R. Hoar , G. D. Johnson , R. P. Larkin , M. D. Strickland , R. W. Threshe , and M. D. Tuttle . 2007. Ecological impacts of wind energy development on bats: questions, research needs, and hypotheses. Frontiers in Ecology and the Environment, 5: 315–324. Google Scholar
  • 39. P. A. Larsen , S. R. Hoofer , M. C. Bozeman , S. C. Pedersen , H. H. Genoways , C. J. Phillips , D. E. Pumo , and R. J. Baker . 2007. Phylogenetics and phylogeography of the Artibeus jamaicensis complex based on cytochrome-b DNA sequences. Journal of Mammalogy, 88: 712–727. Google Scholar
  • 40. P. A. Larsen , M. R. Marchán-Rivadeneira , and R. J. Baker . 2010a. Natural hybridization generates mammalian lineage with species characteristics. Proceedings of the National Academy of Sciences, 107: 11447–11452. Google Scholar
  • 41. P. A. Larsen , M. R. Marchán-Rivadeneira , and R. J. Baker . 2010b. Taxonomic status of Andersen's fruit-eating bat (Artibeus jamaicensis aequatorialis) and revised classification of Artibeus (Chiroptera: Phyllostomidae). Zootaxa, 2648: 45–60. Google Scholar
  • 42. B. K. Lim , M. D. Engstrom , T. E. Lee Jr ., J. C. Patton , and J. W. Bickham . 2004. Molecular differentiation of large species of fruit-eating bats (Artibeus) and phylogenetic relationships based on the cytochrome b gene. Acta Chiropterologica, 6: 1–12. Google Scholar
  • 43. H. S. Maharadatunkamsi , D. J. Kitchener , and L. H. Schmitt 2000. Genetic and morphometric diversity in Wallacea: geographical patterning in the horseshoe bat, Rhinolophus affinis. Journal of Biogeography, 27: 193–201. Google Scholar
  • 44. M. A. Martínez-Morales 1999. Conservation status and habitat preferences of the Cozumel curassow. Condor, 101: 14–20. Google Scholar
  • 45. M. A. Martínez-Morales , P. C. Cruz , and A. D. Cuarón . 2009. Predicted population trends for Cozumel Curassows (Crax rubra griscomi): empirical evidence and predictive models in the face of climate change. Journal of Field Ornithology, 80: 317–327. Google Scholar
  • 46. G. F. McCracken , and G. S. Wilkinson . 2000. Bat mating systems. Pp. 321–362, in Reproductive biology of bats ( E. G. Crichton and P. H. Krutzsch , eds.). Academic Press, New York, NY, 510 pp. Google Scholar
  • 47. R. A. Medellín , H. T. Arita , and O. Sánchez . 1997. Identificación de los murciélagos de México. Asociación Mexicana de Mastozoología, A.C., México, 75 pp. Google Scholar
  • 48. P. G. Meirmans 2006. Using the AMO VA framework to estimate a standardized genetic differentiation measure. Evolution, 60: 2399–2402. Google Scholar
  • 49. C. F. J. Meyer , E. K. V. Kalko , and G. Kerth . 2009. Smallscale fragmentation effects on local genetic diversity in two phyllostomid bats with different dispersal abilities in Panama. Biotropica, 41: 95–102. Google Scholar
  • 50. C. M. Miller-Butterworth , D. S. Jacobs , and E. H. Harley . 2003. Strong population substructure is correlated with morphology and ecology in a migratory bat. Nature, 424: 187–191. Google Scholar
  • 51. R. A. Muscarella , K. L. Murray , D. Ortt , A. L. Russell , and T. H Fleming . 2011. Exploring demographic, physical, and historical explanations for the genetic structure of two lineages of Greater Antillean bats. PLoS ONE, 6(3): e17704. Google Scholar
  • 52. M. Nei 1978. Estimation of average heterozygosity and genetic distance from a small number of individuals. Genetics, 89: 583–590. Google Scholar
  • 53. L. R. Newton , J. M. Nassar , and T. H. Fleming . 2003. Genetic population structure and mobility of two nectar-feeding bats from Venezuelan deserts: Inferences from mitochondrial DNA. Molecular Ecology, 12: 3191–3198. Google Scholar
  • 54. J. Ortega , and H. T. Arita . 1999. Structure and social dynamics of harem groups in Artibeus jamaicensis (Chiroptera: Phyllostomidae). Journal of Mammalogy, 80: 1173–1185. Google Scholar
  • 55. J. Ortega , and I. Castro-Arellano . 2001. Artibeus jamaicensis. Mammalian Species, 662: 1–9. Google Scholar
  • 56. J. Ortega , and J. E. Maldonado . 2006. Female interactions in harem groups of the Jamaican fruit-eating bat, Artibeus jamaicensis (Chiroptera: Phyllostomidae). Acta Chiropterologica, 8: 485–495. Google Scholar
  • 57. J. Ortega , J. E. Maldonado , H. T. Arita , G. S. Wilkinson , and R. C. Fleischer . 2002. Characterization of microsatellite loci in the Jamaican fruit-eating bat Artibeus jamaicensis and cross-species amplification. Molecular Ecology, 2: 462–464. Google Scholar
  • 58. J. Ortega , J. E. Maldonado , G. S. Wilkinson , H. T. Arita , and R. C. Fleischer . 2003. Male dominance, paternity and relatedness in the Jamaican fruit-eating bat (Artibeus jamaicensis). Molecular Ecology, 12: 2409–2415. Google Scholar
  • 59. D. Paetkau , R. Slade , M. Burden , and A. Estoup . 2004. Genetic assignment methods for the direct, real-time estimation of migration rate: a simulation-based exploration of accuracy and power. Molecular Ecology, 13: 55–65. Google Scholar
  • 60. H. Panyu , L. Zhang , G. Zhu , G. Jones , S. Y. Zhang , and S. J. Rossiter . 2011. Hierarchical polygyny in multiparous lesser flat-headed bats. Molecular Ecology, 20: 3669–3680. Google Scholar
  • 61. R. Peakall , and P. E. Smouse . 2006. GENALEX 6: genetic analysis in Excel. Population genetics software for teaching and research. Molecular Ecology Notes, 6: 288–295. Google Scholar
  • 62. S. Piry , A. Alapetite , J. M. Cornuet , D. Paetkau , L. Baudouin , and A. Estoup . 2004. GENECLASS 2: a software for genetics assignment and first-generation migrant detections. Journal of Heredity, 95: 536–539. Google Scholar
  • 63. D. E. Pumo , E. Z. Goldin , B. Elliot , C. J. Phillips , and H. H. Genoways . 1988. Mitochondrial DNA polymorphism in three Antillean island populations of the fruit bat, Artibeus jamaicensis. Molecular Biology and Evolution, 5: 79–89. Google Scholar
  • 64. D. E. Pumo , I. Kim , J. Remsen , C. J. Phillips , and H. H. Genoways . 1996. Molecular systematics of the fruit bat, Artibeus jamaicensis: origin of an unusual island population. Journal of Mammalogy, 77: 491–503. Google Scholar
  • 65. M. Raymond , and F. Rousset . 1995. GenePop v1.2: population genetics software for exact test and ecumenicism. Journal of Heredity, 86: 248–249. Google Scholar
  • 66. F. A. Reid 1997. A field guide to the mammals of Central America and southeast Mexico. Oxford University Press, New York, NY, 334 pp. Google Scholar
  • 67. W. R. Rice 1989. Analyzing tables of statistical tests. Evolution, 43: 223–225. Google Scholar
  • 68. I. Romero-Nájera , A. D. Cuarón , and C. González-Baca . 2007. Distribution, abundance, and habitat use of introduced Boa constrictor threatening the native biota of Cozumel Island, Mexico. Biodiversity and Conservation, 16: 1183–1195. Google Scholar
  • 69. S. J. Rossiter , G. Jones , R. D. Ransome , and E. M. Barratt . 2000. Parentage, reproductive success and breeding behaviour in the greater horseshoe bat (Rhinolophus ferrumequinum). Proceedings of the Royal Society of London, 267B: 545–551. Google Scholar
  • 70. S. J. Rossiter , A. Zubaid , A. Mohd-Adnan , M. J. Struebig , T. H. Kunz , S. Gopal , E. J. Petit , and T. Kingston . 2012. Social organization and genetic structure: insights from codistributed bat populations. Molecular Ecology, 21: 647–661. Google Scholar
  • 71. R. S. Sikes , W. L. Gannon , and the Animal Care and Use Committee of the American Society of Mammalogists. 2011. Guidelines of the American Society of Mammalogists for the use of wild mammals in research. Journal of Mammalogy, 92: 235–253. Google Scholar
  • 72. S. F. Spear , and A. Storfer . 2010. Anthropogenic and natural disturbance lead to differing patterns of gene flow in the Rocky Mountain tailed frog, Ascaphus montanus. Biological Conservation, 143: 778–786. Google Scholar
  • 73. J. F. Storz , H. R. Bhat , and T. H. Kunz . 2001. Genetic consequences of polygyny and social structure in an Indian fruit bat, Cynopterus sphinx II. Variance in male mating success and effective population size. Evolution, 55: 1224–1232. Google Scholar
  • 74. M. J. Struebig , T. Kingston , E. J. Petit , S. C. Le Comber , A. Zubaid , A. Mohd-Adnan , and S. J. Rossiter . 2011. Parallel declines in species and genetic diversity in tropical forest fragments. Ecology Letters, 14: 582–590. Google Scholar
  • 75. O. Téllez-Valdés , E. F. Cabrera , E. Linares , and R. Bye . 1989. Las plantas de Cozumel. Guía botánico-turística de la isla de Cozumel, Quintana Roo. Instituto de Biología, Universidad Nacional Autónoma de México, México, 75 pp. Google Scholar
  • 76. C. van Oosterhout , W. F. Hutchinson , D. P. M. Willis , and P. Shipley . 2004. MICRO-CHECKER: software for identifying and correcting genotyping error in microsatellite data. Molecular Ecology Notes, 4: 535–538. Google Scholar
  • 77. E. Vázquez-Domínguez , D. Paetkau , N. J. Tucker , G. Hinten , and C. Moritz . 2001. Resolution of natural groups using iterative assignment tests: an example from two species of Australian native rats (Rattus). Molecular Ecology, 10: 2069–2078. Google Scholar
  • 78. E. Vázquez-Domínguez , G. Ceballos , and J. Cruzado . 2004. Extirpation of an insular subspecies by a single introduced cat: the case of the endemic deer mouse Peromyscus guardia on Estanque Island, Mexico. Oryx, 38: 347–350. Google Scholar
  • 79. E. Vázquez-Domínguez , M. Suárez-Atilano , W. Booth , C. González-Baca , and A. D. Cuarón . 2012. Genetic evidence of a recent successful colonization of introduced species on islands: Boa constrictor imperator on Cozumel Island. Biological Invasions, 14: 2101–2116. Google Scholar
  • 80. R. Vega , E. Vázquez-Domínguez , A. Mejía-Puente , and A. D. Cuarón . 2007. Unexpected high levels of genetic variability and the population structure of an island endemic rodent (Oryzomys couesi cozumelae). Biological Conservation, 137: 210–222. Google Scholar
  • 81. M. J. Vonhof , C. Strobeck , and M. B. Fenton . 2008. Genetic variation and population structure in big brown bats (Eptesicus fiuscus): is female dispersal important? Journal of Mammalogy, 89: 1411–1419. Google Scholar
  • 82. Y. Q. Wang , D. A. Williams , and M. S. Gaines . 2005. Evidence for a recent genetic bottleneck in the endangered Florida Keys silver rice rat (Oryzomys argentatus) revealed by microsatellite DNA analyses. Conservation Genetics, 6: 575–585. Google Scholar
  • 83. B. S. Weir , and C. C. Cockerham . 1984. Estimating F-statistics for the analysis of population structure. Evolution, 38: 1358–1370. Google Scholar
  • 84. D. E. Wilson , and D. M. Reeder (eds.). 1993. Mammal species of the World: a taxonomic and geographic reference, 2nd edition. Smithsonian Institution Press, Washington, D.C., 1207 pp. Google Scholar
  • 85. J. Worthington Wilmer , L. Hall , E. Barratt , and C. Moritz . 1999. Genetic structure and male mediated gene flow in the ghost bat (Macroderma gigas). Evolution, 53: 1583–1591. Google Scholar
  • 86. F. C. Yeh , R. Yang , and T. Boyle . 1999. POPGENE v.1.31. Microsoft windows-based freeware for population genetic analysis. University of Alberta, Alberta, Canada. Google Scholar
  • 87. H. Yoshino , K. N. Armstrong , M. Izawa , J. Yokoyama , M. Kawata . 2008. Genetic and acoustic population structuring in the Okinawa least horseshoe bat: are intercolony acoustic differences maintained by vertical maternal transmission? Molecular Ecology, 17: 4978–4991. Google Scholar

Uwagi

Rekord w opracowaniu

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-5cabe845-3a9b-4d0a-8758-149b850af33b
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.