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Genetic variation and differentiation in Indirana beddomii frogs endemic to the Western Ghats biodiversity hotspot

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Abstract

Understanding of biodiversity on a local scale is extremely important for effective conservation measures, especially in biodiversity hotpsots hosting diverse endemic flora and fauna and subject to strong anthropogenic influences. Little is known about patterns of local biodiversity and the processes generating it in the Western Ghats biodiversity hotspot: the patterns of genetic diversity and biogeographic affinities are poorly known for most of the species from this region. We studied the genetic diversity and population structuring of an endemic frog Indirana cf beddomii, from 12 localities of Western Ghats using 15 polymorphic microsatellite loci. The genetic diversity as measured by mean expected heterozygosity (H E = 0.83) or allelic richness (A r = 10.41) was high and similar in all localities. Significant genetic differentiation (mean F ST = 0.075) with a strong pattern of isolation by distance (IBD) across the localities was observed. Clearest genetic discontinuities in the data corresponded to topographic gaps suggesting that apart from IBD, genetic structuring in this species is strongly influenced by habitat matrix. In general, the results provide novel insight into factors that may impact the genetic diversity and population structuring of endemic amphibians in this biodiversity hotspot.

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References

  • Andersen LW, Fog K, Damgaard C (2004) Habitat fragmentation causes bottlenecks and inbreeding in the European tree frog (Hyla arborea). Proc R Soc B 271:1293–1302

    Article  PubMed  Google Scholar 

  • Bahulikar RA, Lagu MD, Kulkarni BG, Pandit SS, Suresh HS et al (2004) Genetic diversity among spatially isolated populations of Eurya nitida Korth. (Theaceae) based on inter-simple sequence repeats. Curr Sci 86:824–831

    CAS  Google Scholar 

  • Baskaran N, Anbarasan U, Agoramoorthy G (2012) India’s biodiversity hotspot under anthropogenic pressure: a case study of Nilgiri biosphere reserve. J Nat Conserv 20:56–61

    Article  Google Scholar 

  • Biju SD (2001) A synopsis to the frog fauna of the Western Ghats, India. Occas Publ Indian Soc Conserv Biol 1:1–24

    Google Scholar 

  • Biju SD, Bossuyt F (2003) New frog family from India reveals an ancient biogeographical link with the Seychelles. Nature 425:711–714

    Article  PubMed  CAS  Google Scholar 

  • Biju SD, Bossuyt F (2009) Systematics and phylogeny of Philautus Gistel, 1848 (Anura, Rhacophoridae) in the Western Ghats of India, with descriptions of 12 new species. Zool J Linn Soc 155:374–444

    Article  Google Scholar 

  • Biju SD, Kamei R, Bhatta G, Giri V, Cox N, Das I, Bossuyt F (2008) Diversity and conservation status of the Western Ghats amphibians. In: Stuart SN, Hoffmann M, Chanson JS, Cox NA, Berridge R, Ramani P, Young BE (eds) Threatened amphibians of the world. Lynx Edicions, Barcelona, pp 80–82

    Google Scholar 

  • Biju SD, Bocxlaer IV, Mahony S, Dinesh KP, Radhakrishnan C, Zachariah A, Giri V, Bossuyt F (2011) A taxonomic review of the Night Frog genus Nyctibatrachus Boulenger, 1882 in the Western Ghats, India (Anura: Nyctibatrachidae) with description of twelve new species. Zootaxa 3029:1–96

    Google Scholar 

  • Bocxlaer IV, Biju SD, Willaert B, Giri VB, Shouche YS, Bossuyt F (2012) Mountain-associated clade endemism in an ancient frog family (Nyctibatrachidae) on the Indian subcontinent. Mol Phylogenet Evol 62:839–847

    Article  PubMed  Google Scholar 

  • Bossuyt F, Meegaskumbura M, Beenaerts N, Gower DJ, Pethiyagoda R, Roelants K, Mannaert A, Wilkinson M, Bahir MM, Manamendra-Arachchi K, Ng PKL, Schneider CJ, Oomen OV, Milinkovitch MC (2004) Local endemism within the Western Ghats–Sri Lanka biodiversity hotspot. Science 306:479–481

    Article  PubMed  CAS  Google Scholar 

  • Boulenger GA (1920) A monograph of the South Asian, Papuan, Melanesian and Australian frogs of the genus Rana. Rec Indian Mus 20:1–226

    Google Scholar 

  • Brooks TM, Mittermeier RA, Mittermeier CG, da Fonseca GAB, Rylands AB, Konstant WR, Flick P, Pilgrim J, Oldfield S, Magin G, Hilton-Taylor C (2002) Habitat loss and extinction in the hotspots of biodiversity. Conserv Biol 16:909–923

    Article  Google Scholar 

  • Brownstein MJ, Carpten JD, Smith JR (1996) Modulation of non-templated nucleotide addition by Taq DNA polymerase: primer modifications that facilitate genotyping. Biotechniques 20:1004–1010

    PubMed  CAS  Google Scholar 

  • Cincotta RP, Wisnewski J, Engelman R (2000) Human population in the biodiversity hotspots. Nature 404:990–992

    Article  PubMed  CAS  Google Scholar 

  • Cornuet JM, Luikart G (1996) Description and power analysis of two tests for detecting recent population bottlenecks from allele frequency data. Genetics 144:2001–2014

    PubMed  CAS  Google Scholar 

  • Daniel JC, Sekar AG (1989) Field guide to the amphibians of Western India. J Bombay Nat Hist Soc 86:194–202

    Google Scholar 

  • Daniels RJR (1997) Taxonomic uncertainties and conservation assessment of the Western Ghats. Curr Sci 73:169–170

    Google Scholar 

  • Daniels RJR (2005) Amphibians of peninsular India. Universities Press (India) Pvt Ltd, Hyderabad

    Google Scholar 

  • Das A, Krishnaswamy J, Bawa KS, Kiran MC, Srinivas V, Kumar NS, Karanth U (2006) Prioritisation of conservation areas in the Western Ghats, India. Biol Conserv 133:16–31

    Article  Google Scholar 

  • Davidar P, Arjunan M, Mammen PC, Garrigues JP, Puyravaud JP, Roessingh K (2007) Forest degradation in the Western Ghats biodiversity hotspot: resource collection, livelihood concerns and sustainability. Curr Sci 93:1573–1578

    Google Scholar 

  • DeChaine E, Martin A (2005) Marked genetic divergence among sky island populations of Sedum lanceolatum (Crassulaceae) in the Rocky Mountains. Am J Bot 92:477–486

    Article  PubMed  CAS  Google Scholar 

  • Deshpande AU, Apte GS, Bahulikar RA, Lagu MD, Kulkarni BG et al (2001) Genetic diversity across natural populations of three montane plant species from the Western Ghats, India revealed by inter-simple sequence repeats. Mol Ecol 10:2397–2408

    Article  PubMed  CAS  Google Scholar 

  • Di Rienzo A, Peterson AC, Garza JC et al (1994) Mutational processes of simple-sequence repeat loci in human populations. Proc Natl Acad Sci USA 91:3166–3170

    Article  PubMed  Google Scholar 

  • Dixo M, Metzger JP, Morgante JS, Zamudio KR (2009) Habitat fragmentation reduces genetic diversity and connectivity among toad populations in the Brazilian Atlantic coast forest. Biol Conserv 142:1560–1569

    Article  Google Scholar 

  • Dutta SK (1997) Amphibians of India and Sri Lanka. Odyssey Publishing House, Bhubaneswar

    Google Scholar 

  • Evanno G, Regnaut S, Goudet J (2005) Detecting the number of clusters of individuals using the software structure: a simulation study. Mol Ecol 14:2611–2620

    Article  PubMed  CAS  Google Scholar 

  • Fahrig L (2003) Effects of habitat fragmentation on biodiversity. Annu Rev Ecol Evol Syst 34:487–515

    Article  Google Scholar 

  • Goudet J (1995) FSTAT (version 1.2): a computer program to calculate F-statistics. J Hered 86:485–486

    Google Scholar 

  • Gower D, Dharne M, Bhatta G, Giri V, Vyas R, Govindappa V, Oommen OV, George J, Shouche Y, Wilkinson M (2007) Remarkable genetic homogeneity in unstriped, long-tailed Ichthyophis along 1500 km of the Western Ghats, India. J Zool 272:266–275

    Article  Google Scholar 

  • Guillot G, Mortier F, Estoup A (2005a) GENELAND: a computer package for landscape genetics. Mol Ecol Notes 5:712–715

    Article  CAS  Google Scholar 

  • Guillot G, Estoup A, Mortier F, Cosson J-F (2005b) A spatial model for landscape genetics. Genetics 170:1261–1280

    Article  PubMed  CAS  Google Scholar 

  • Günther A (1876) Third report on collection of Indian reptiles obtained by the British Museum. Proc Zool Soc Lond 1875:567–577

    Google Scholar 

  • Henle K, Lindenmayer DB, Margules CR, Saunders DA, Wissel C (2004) Species survival in fragmented landscapes: where are we now? Biodivers Conserv 13:1–8

    Article  Google Scholar 

  • Hoffmann M, Hilton-Taylor C, Angulo A, Böhm M et al (2010) The impact of conservation on the status of the World’s vertebrates. Science 330:1503–1509

    Article  PubMed  CAS  Google Scholar 

  • Inger RF (1999) Distribution of amphibians in southern Asia and adjacent islands. In: Duellman WE (ed) Patterns of distribution of amphibians: a global perspective. Johns Hopkins University Press, London, pp 445–482

    Google Scholar 

  • Inger RF, Shaffer HB, Koshy M, Bakde R (1984) A report on a collection of amphibians and reptiles from Ponmudi, Kerala, South India. J Bombay Nat Hist Soc 81:406–427

    Google Scholar 

  • Jha CS, Dutt CBS, Bawa KS (2000) Deforestation and land use changes in Western Ghats, India. Curr Sci 79:231–238

    Google Scholar 

  • Johansson M, Primmer CR, Merilä J (2007) Does habitat fragmentation reduce fitness and adaptability? A case study of the common frog (Rana temporaria). Mol Ecol 16:2693–2700

    Article  PubMed  Google Scholar 

  • Krishnankutty N, Chandrasekaran S (2007) Biodiversity hotspots: defining the indefinable? Curr Sci 92:1344–1345

    Google Scholar 

  • Langella O (2002) Populations 1.2.28. Logiciel de génétique des populations. Laboratoire Populations, génétique et évolution, CNRS UPR9034, Gif-sur-Yvette

  • Luikart G, Allendorf FW, Cornuet JM, Sherwin WB (1998) Distortion of allele frequency distributions provides a test for recent population bottlenecks. J Hered 89:238–247

    Article  PubMed  CAS  Google Scholar 

  • Mantel N (1967) The detection of disease clustering and a generalized regression approach. Cancer Res 27:209–220

    PubMed  CAS  Google Scholar 

  • Myers N, Mittermeier RA, Mittermeier CG, da Fonseca GAB, Kent J (2000) Biodiversity hotspots for conservation priorities. Nature 403:853–858

    Article  PubMed  CAS  Google Scholar 

  • Nair A, Kumar KS, George S, Gopalan SV, Li M-H, Leder E, Merilä J (2011) Sixty two new microsatellite markers for an endemic frog Indirana beddomii from the Western Ghats biodiversity hotspot. Conserv Genet Resour 3:167–171

    Article  Google Scholar 

  • Nair A, Gopalan SV, George S, Kumar KS, Teacher AGF, Merilä J (2012a) High cryptic diversity of endemic Indirana frogs in the Western Ghats biodiversity hotspot. Anim Conserv. doi:10.1111/j.1469-1795.2012.00539.x

    Google Scholar 

  • Nair A, Gopalan SV, George S, Kumar KS, Merilä J (2012b) Cross-species testing and utility of microsatellite loci in Indirana frogs. BMC Res Notes 5:389. doi:10.1186/1756-0500-5-389

  • Nei M, Tajima F, Tateno Y (1983) Accuracy of estimated phylogenetic trees from molecular data. J Mol Evol 19:153–170

    Article  PubMed  CAS  Google Scholar 

  • Peakall R, Smouse PE (2006) GENALEX 6: genetic analysis in excel. Population genetic software for teaching and research. Mol Ecol Notes 6:288–295

    Article  Google Scholar 

  • Piry S, Luikart G, Cornuet JM (1999) BOTTLENECK: a computer program for detecting recent reductions in the effective population size using allele frequency data. J Hered 90:502–503

    Article  Google Scholar 

  • Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155:945–959

    PubMed  CAS  Google Scholar 

  • Robin VV, Sinha A, Ramakrishnan U (2010) Ancient geographical gaps and Paleo-climate shape the phylogeography of an endemic bird in the sky islands of Southern India. PLoS One 5:e13321

    Article  PubMed  CAS  Google Scholar 

  • Roelants K, Jiang J, Bossuyt F (2004) Endemic ranid (Amphibia: Anura) genera in southern mountain ranges of the Indian subcontinent represent ancient frog lineages: evidence from the molecular data. Mol Phylogenet Evol 31:730–740

    Article  PubMed  CAS  Google Scholar 

  • Rousset F (2008) Genepop ‘007: a complete re-implementation of the genepop software for Windows and Linux. Mol Ecol Notes 8:103–106

    Google Scholar 

  • Stuart SN, Chanson JS, Cox NA, Young BE, Rodrigues ASL, Fischman DL, Waller RW (2004) Status and trends of amphibian declines and extinctions worldwide. Science 306:1783–1786

    Article  PubMed  CAS  Google Scholar 

  • Takezaki M, Nei M (1996) Genetic distances and reconstruction of phylogenetic trees from microsatellite DNA. Genetics 144:389–399

    PubMed  CAS  Google Scholar 

  • Van Oosterhout C, Hutchinson WF, Wills DP, Shipley P (2004) MICRO-CHECKER: software for identifying and correcting genotyping errors in microsatellite data. Mol Ecol Notes 4:535–538

    Article  Google Scholar 

  • Veeranagoudar DK, Radder RS, Shanbhag BA, Saidapur SK (2009) Jumping behavior of semiterrestrial tadpoles of Indirana beddomii (Günth.): relative importance of tail and body size. J Herpetol 43:680–684

    Article  Google Scholar 

  • Vidya T, Fernando P, Melnick D, Sukumar R (2005) Population differentiation within and among Asian elephant (Elephas maximus) populations in southern India. Heredity 94:71–80

    Article  PubMed  CAS  Google Scholar 

  • Warshall P (1995) The Madrean Sky Island Archipelago: a planetary overview. In: DeBano LF, Ffolliott PF, Ortega-Rubio A, Gottfried GJ, Hamre RH, Edminster CB (eds) Biodiversity and management of the Madrean Archipelago: the Sky Islands of southwestern United States and northwestern Mexico. USDA General Technical Report RM-GTR 264, Fort Collins, pp 6–18

  • Weir BS, Cockerham CC (1984) Estimating F-statistics for the analysis of population structure. Evolution 38:1358–1370

    Article  Google Scholar 

  • Wikramanayake E, Dinerstein E, Loucks C (2001) Terrestrial ecoregions of the Indo-Pacific: a conservation assessment. Island Press, Washington

    Google Scholar 

  • Zhan A, Li C, Fu J (2009) Big mountains but small barriers: population genetic structure of the Chinese wood frog (Rana chensinensis) in the Tsinling and Daba mountain region of northern China. BMC Genet 10:17

    Article  PubMed  Google Scholar 

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Acknowledgments

We are grateful to Kerala and Karnataka Forest Departments for permissions for sample collections. Thanks to Vinodlal K. S., Vijayan P. and Biju S. Nair for help with the field work. The samples were collected under licence from National Biodiversity Authority, India (Licence #: NBA/TECH Appl/9/85/34/08/08-09/682). Our research was funded by Academy of Finland (Grant #125092 to JM) and Department of Biotechnology, Government of India (BT/IN/Finnish/11/SG/2008 to SG).

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Correspondence to Abhilash Nair.

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Nair, A., Gopalan, S.V., George, S. et al. Genetic variation and differentiation in Indirana beddomii frogs endemic to the Western Ghats biodiversity hotspot. Conserv Genet 13, 1459–1467 (2012). https://doi.org/10.1007/s10592-012-0389-z

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