Abstract
The Eastern Afromontane biodiversity hotspot consists of isolated mountain massifs embedded within the dry lowland savannas of East Africa and of which the peaks and ridges are covered by cloud forest remnants. These cloud forests are home to the Mountain White-eye (Zosterops poliogaster), while three congeneric species (Abyssinian White-eye, Zosterops abyssinicus; Yellow White-eye, Zosterops senegalensis; Pemba White-eye, Zosterops vaughani) inhabit the adjacent lowland savannas. We sampled individuals of all four species across Kenya to analyse interspecific genetic relationships as well as intraspecific differentiation among mountain populations of Z. poliogaster. While the level of genetic differentiation among the four species was rather low, genetic differentiation within Z. poliogaster was very high, even between geographically neighbouring populations. Overall, levels of genetic variation varied strongly across all four species, with much higher diversity detected within the three lowland ones. The highland species was characterised by numerous private alleles that were geographically restricted at populations from single mountains, some of which showed evidence of recent population bottlenecks. We conclude that Z. poliogaster populations are both of high conservation value and conservation concern, given the high proportion of endemic alleles and the genetic signatures of high genetic drift and low gene flow that are typical for small and isolated populations.
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References
Bennun L, Njoroge P (1999) Important bird areas in Kenya. Polarprint, East Africa Natural History Society, Nairobi
Bennun L, Davies G, Howell K, Newing H, Linkie M (2002) African biodiversity: a field survey manual for vertebrates. Birdlife International, Cambridge, p 161
Bowie RCK, Voelker G, Fjeldsa J, Lens L, Hackett SJ, Crowe TM (2005) Systematics of the olive thrush Turdus olivaceus species complex with reference to the taxonomic status of the endangered Taita thrush T. helleri. J Avian Biol 36:391–404
Bowie RCK, Fjeldsa J, Hackett SJ, Bates JM, Crowe TM (2006) Coalescent models reveal the relative roles of ancestral polymorphism, vicariance, and dispersal in shaping phylogeographical structure of an African montane forest robin. Mol Phylogenet Evol 38:171–188
Burgess ND, Butynski TM, Cordeiro NJ, Doggart NH, Fjeldså J, Howell KM, Kilahama FB, Loader SP, Lovett JC, Mbilinyi B, Menegon M, Moyer DC, Nashanda E, Perkin A, Rovero F, Stanley WT, Stuart SN (2007) The biological importance of the Eastern Arc Mts. of Tanzania and Kenya. Biol Conserv 34:209–231
Caizergues A, Bernard-Laurent A, Brenot JF, Ellison L, Rasplus JY (2003) Population genetic structure of rock ptarmigan Lagopus mutus in Northern and Western Europe. Mol Ecol 12:2267–2274
Callens T, Galbusera P, Matthysen E, Durand EY, Githiru M, Huyghe JR, Lens L (2011) Genetic signature of population fragmentation varies with mobility in seven bird species of a fragmented Kenyan cloud forest. Mol Ecol 20:1829–1844
Chege J, Bytebier B (2005) Vegetation structure of four small forest fragments in Taita Hills, Kenya. J East Afr Nat Hist 94:231–234
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
Crochet PA (2000) Genetic structure of avian populations—allozymes revisited. Mol Ecol 9:1463–1469
Degnan SM, Robertson BC, Clegg SM, Moritz CC (1999) Microsatellite primers for studies of gene flow and mating systems in white-eyes (Zosterops). Mol Ecol 8:157–168
Ehrich D, Gaudeul M, Assefa A, Koch MA, Mummenhoff K, Nemomissa S, Intrabiodiv consortium, Brochmann C (2007) Genetic consequences of Pleistocene range shifts: contrast between the Artic the Alps and the East African mountains. Mol Ecol 16:2542–2559
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
Excoffier L, Larval G, Schneider S (2005) Arlequin ver. 3.0: an integrated software package for population genetics data analysis. Evol Bioinform Online 1:47–50
Frankham R, Gilligan DM, Morris D, Briscoe DA (2001) Inbreeding and extinction: effects of purging. Conserv Genet 2:279–285
Frentiu FD, Lange CL, Burke T, Owens IPF (2003a) Isolation of microsatellite loci in the Capricorn silvereye, Zosterops lateralis chlorocephalus (Aves: Zosteropidae). Mol Ecol Notes 3:462–464
Frentiu FD, Lange CL, Burke T, Owens IPF (2003b) Isolation of microsatellite loci in the Capricorn silvereye, Zosterops lateralis chlorocephalus (Aves: Zosteropidae). Mol Ecol Notes 3:462–464
Galbusera P, Lens L, Schenck T, Waiyaki E, Matthysen E (2000a) Genetic variability and gene flow in the globally critically endangered Taita thrush. Conserv Genet 1:45–55
Galbusera P, van Dongen S, Matthysen E (2000b) Cross-species amplification of microsatellite primers in passerine birds. Conserv Genet 1:163–168
Goudet J (1995) FSTAT Ver. 1.2: a computer programm to calculate F-statistics. Heredity 86:485–486
Habel JC, Schmitt T (2012) The burden of genetic diversity. Biol Conserv 147:270–274
Habel JC, Zachos F (2012) Habitat fragmentation versus fragmented habitats. Biodivers Conserv 21:2987–2990
Hatchwell BJ (2009) The evolution of cooperative breeding in birds: kinship, dispersal and life history. Phil Trans R Soc Biol Sci 364:3217–3227
Hausdorf B, Hennig C (2010) Species delimitation using dominant and codominant multilocus markers. Syst Biol 59:491–503
Hill T, Lewicki P (2007) Statistics: methods and applications. StatSoft, Tulsa
Jeffery KJ, Keller LF, Arcese P, Bruford MW (2001) The development of microsatellite loci in the song sparrow, Melospiza melodia (Aves) and genotyping errors associated with good quality DNA. Mol Ecol Notes 1:11–13
Keyghobadi N (2007) The genetic implications of habitat fragmentation for animals. Can J Zool 85:1049–1064
Luikart G, Cornuet J-M (1998) Empirical evaluation of a test for identifying recently bottlenecked populations from allele frequency data. Conserv Biol 12:228–237
Martin TE, Roper JR (1988) Nest predation and nest-site selection of a western population of the hermit thrush. Condor 90:51–57
Measey GJ, Tolley KA (2011) Sequential fragmentation of Pleistocene forests in an East Africa biodiversity hotspot: chameleons as a model to track forest history. PLoS ONE 6:e26606
Measey GJ, Galbusera P, Brayne P, Matthysen E (2007) Gene flow in a direct developing, leaf litter frog between isolated mountains in the Taita Hills, Kenya. Conserv Genet 8:1177–1188
Moore RP, Robinson WD, Lovette IJ, Robinson TR (2008) Experimental evidence for extreme dispersal limitation in tropical forest birds. Ecol Lett 11:960–968
Mulwa RK, Bennun LA, Ogol CPK, Lens L (2007) Population status and distribution of Taita White-eye Zosterops silvanus in the fragmented forests of Taita Hills and Mount Kasigau, Kenya. Bird Conserv Int 17:141–150
Myers N (1990) The biodiversity challenge: expanded hot-spots analysis. Environmentalist 10:243–256
Pellikka PKE, Lötjönen M, Siljander M, Lens L (2009) Airborne remote sensing of spatiotemporal change (1955–2004) in indigenous and exotic forest cover in the Taita Hills, Kenya. Int J Appl Earth Obs Geoinf 11:221–232
Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155:945–955
Redman N, Stevenson T, Fanshawe J (2009) The birds of the horn of Africa. Christopher Helm, London
Sieving K (1992) Nest predation and differential insular extinction among selected forest birds of central Panama. Ecology 73:2310–2328
Slatkin M (1995) A measure of population subdivision based on microsatellite allele frequencies. Genetics 139:457–462
Stratford A, Robinson WD (2005) Gulliver travels to the fragmented tropics: geographic variation in mechanisms of avian extinction. Front Ecol Environ 3:85–92
Taylor PD, Fahrig L, Henein K, Merriam G (1993) Connectivity Is a Vital Element of Landscape Structure. Oikos 68:571–573
Van Oosterhout C et al (2004) MICRO-CHECKER (version 2.2.3): software for identifying and correcting genotyping errors in microsatellite data. Mol Ecol Notes 4:535–538
Walker FM, Sunnucks P, Taylor AC (2008) Evidence for habitat fragmentation altering within-population processes in wombats. Mol Ecol 17:1674–1684
White F (1978) The afromontane region. In: Werger MJA (ed) Biogeography and ecology of southern Africa. Junk, The Hague, pp 463–513
Wilcove DS (1985) Nest predation in forest tracts and the decline of migratory songbirds. Ecology 66:1211–1214
Wilson GA, Rannala B (2003) Bayesian inference of recent migration rates using multilocus genotypes. Genetics 163:1177–1191
Zimmermann DA, Turner DA, Person DJ (1996) Birds of Kenya and Northern Tanzania. Christopher Helm, London
Acknowledgments
This study was funded by the German Academic Exchange Service (DAAD), the Natural History Museum Luxembourg, the Research Foundation Flanders (FWO) (grants G.0055.08 to LL and G.0149.09 to S. Van Dongen) and the Flemish Interuniversity Council (project 02/6/7-338-607 to W. Verheyen) as well as by FWO research communities (WO.037.10N to F. Volckaert). We are grateful for helpful advice by Ulrike Schülter (Trier, Germany) in the laboratory. We thank Dennis Rödder (Bonn, Germany) for creating Fig. 1. We thank Martin Husemann (Waco, USA) and two anonymous referees for helpful comments on two draft versions of this manuscript.
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Habel, J.C., Cox, S., Gassert, F. et al. Population genetics of the East African White-eye species complex. Conserv Genet 14, 1019–1028 (2013). https://doi.org/10.1007/s10592-013-0492-9
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DOI: https://doi.org/10.1007/s10592-013-0492-9