Abstract
Asexual reproduction lacks genetic diversity but is predicted to be advantageous for dispersal and for increasing abundance relative to sexual reproduction. The oceanic Ogasawara Islands are inhabited by two gecko species, the asexual (parthenogenetic) all-female Lepidodactylus lugubris and the sexually reproductive Hemidactylus frenatus. This situation offers a unique opportunity to examine the relationships among sexuality and the abundance, distribution, and genetic diversity of the two species. A total of 445 geckos were collected across nine islands, and the population genetic structure of both species was estimated using microsatellite markers. Lepidodactylus lugubris was collected on all nine islands and consisted of two widely distributed clones: one diploid and the other triploid. In contrast, H. frenatus was limited to four islands and exhibited variation in population genetic structure among islands, with some bottleneck effects. Successful dispersal may be more frequent in L. lugubris than in H. frenatus; therefore, the asexual reproductive strategy of L. lugubris appears to have contributed to its dispersal success and increased abundance among the small oceanic islands. However, the absence of H. frenatus on islands not inhabited by humans may be partially explained by their different microhabitat preferences, as H. frenatus collection sites were relatively more confined to artificial substrates in towns and along roadways compared to L. lugubris. Moreover, the colonization histories of these two geckos have not yet been assessed; therefore, further study is needed to confirm the effects of sexuality on the population dynamics of these species.
Similar content being viewed by others
References
Bolger DT, Case TJ (1994) Divergent ecology of sympatric clones of the asexual gecko, Lepidodactylus lugubris. Oecologia 100:397–405
Cole CJ (1984) Unisexual lizards. Sci Am 250:94–100
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, Lisher HEL (2010) Arlequin suite ver 3.5: a new series of programs to perform population genetics analysis under Linux and Windows. Mol Ecol Resour 10:564–567
Goudet J (1995) FSTAT (version 1.2): a computer program to calculate F-statistics. J Hered 86:485–486
Hanley KA, Bolger DT, Case TJ (1994) Comparative ecology of sexual and asexual gecko species (Lepidodactylus) in French Polynesia. Evol Ecol 8:438–454
Hayashi F, Shima A, Horikoshi K, Kawakami K, Segawa RD, Aotsuka T, Suzuki T (2009) Limited overwater dispersal and genetic differentiation of the snake-eyed skink (Cryptoblepharus nigropunctatus) in the oceanic Ogasawara Islands, Japan. Zool Sci 26:543–549
Horikoshi K (2008) Lizards in Minami-Iwo-To Island. Ogasawara Res 33:129–134 (in Japanese)
Hubisz MJ, Falush D, Stephens M, Prichard JK (2009) Inferring weak population structure with the assistance of sample group information. Mol Ecol Resour 9:1322–1332
Ineich I (1999) Spatio-temporal analysis of the unisexual-bisexual Lepidodactylus lugubris complex (Reptilia, Gekkonidae). In: Ota H (ed) Tropical island herpetofauna: origin, current diversity and conservation. Elsevier, pp 199–228
Ineich I, Ota H (1992) Additional remarks on the unisexual-bisexual complex of the gecko, Lepidodactylus lugubris, in Takapoto Atoll, French Polynesia. Bull Coll Sci Univ Ryukyus 53:31–39
Li J, Zhou K (2007) Isolation and characterization of microsatellite markers in the gecko Gekko swinhonis and cross-species amplification in other gekkonid species. Mol Ecol Notes 7:674–677
Maynard Smith J (1978) The evolution of sex. Cambridge University Press, Cambridge
Moritz C, Case TJ, Bolger DT, Donnellan S (1993) Genetic diversity and the history of pacific island house geckos (Hemidactylus and Lepidodactylus). Biol J Linnean Soc 48:113–133
Neaves WB, Baumann P (2011) Unisexual reproduction among vertebrates. Trends Genet 27:81–88
Newbery B, Jones DN (2007) Presence of Asian house gecko Hemidactylus frenatus across an urban gradient in Brisbane: influence of habitat and potential for impact on native gecko species. In: Lunney D, Eby P, Hutchings P, Burgin S (eds) Pest or guest: the zoology of overabundance. R Zool Soc NSW, Mosman, pp 59–65
Okada Y (1930) Notes on the herpetology of Chichijima, one of the Bonin Islands. Bull Biogeogr Soc Japan 1:187–194
Ota H (1994) Female reproductive cycles in the northernmost populations of the two gekkonid lizards, Hemidactylus frenatus and Lepidodactylus lugubris. Ecol Res 9:121–130
Owusu KA, Detwiler JT, Criscione CD (2012) Characterization of 21 microsatellite loci from the invasive Mediterranean gecko (Hemidactylus turcicus). Conservation Genet Resour 4:563–565
Peakall R, Smouse PE (2012) GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research - an update. Bioinformatics 28:2537–2539
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
Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155:945–959
Radtkey RR, Donnellan SC, Fisher RN, Moritz C, Hanley KA, Case TJ (1995) When species collide: the origin and spread of an asexual species of gecko. Proc R Soc Lond 259:145–152
Rousset F (2008) GENEPOP’007: a complete re-implementation of the Genepop software for Windows and Linux. Mol Ecol Resour 8:103–106
Short KH, Petren K (2008) Boldness underlies foraging success of invasive Lepidodactylus lugubris geckos in the human landscape. Anim Behav 76:429–437
Simon JC, Delmotte F, Rispe C, Crease T (2003) Phylogenetic relationships between parthenogens and their sexual relatives: the possible routes to parthenogenesis in animals. Biol J Linnean Soc 79:151–163
Takada E, Ohtani T (2011) Keys to the illustrated manual of Japanese reptiles and amphibians in natural color. Hokuryukan Co. Ltd., Tokyo (in Japanese)
Weir BS, Cockerham CC (1984) Estimating F–statistics for the analysis of population structure. Evolution 38:1350–1370
Wilmhoff CD, Csepeggi CE, Petren K (2003) Characterization of dinucleotide microsatellite markers in the parthenogenetic mourning gecko (Lepidodactylus lugubris). Mol Ecol Notes 3:400–402
Yamashiro S, Ota H (2005) On the clone type of Lepidodactylus lugubris (Duméril and Bibron 1836) corresponding to Gehyra variegata ogasawarasimae Okada, 1930 (Reptilia: Gekkonidae). Curr Herpetol 24:95–98
Yamashiro S, Toda M, Ota H (2000) Clonal composition of the parthenogenetic gecko, Lepidodactylus lugubris, at the northernmost extremity of its range. Zool Sci 17:1013–1020
Acknowledgments
We thank Hidetoshi Ota and Mamoru Toda for providing relevant information and literature on Lepidodactylus lugubris, and Naoki Kachi, Hidetoshi Kato, Takeshi Osawa, Syuntaro Hiradate, Kosei Hashimoto, Suguru Wakikaido, Ai Takaoka, Akinobu Imamura, and Masahide Kubota for their help with field work. Samples were collected from protected areas with permission of the Ministry of the Environment, Japan.
Author information
Authors and Affiliations
Corresponding author
Electronic supplementary material
Below is the link to the electronic supplementary material.
Table S1 Allele frequencies in five microsatellite loci of Hemidactylus frenatus on four Ogasawara islands. N = number of individuals sampled, N A = number of alleles, H O = observed heterozygosity, H E = expected heterozygosity. Frequencies on the northern, central, and southern parts of Chichijima and Hahajima are also shown separately (see Fig. 3).
About this article
Cite this article
Murakami, Y., Sugawara, H., Takahashi, H. et al. Population genetic structure and distribution patterns of sexual and asexual gecko species in the Ogasawara Islands. Ecol Res 30, 471–478 (2015). https://doi.org/10.1007/s11284-015-1246-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11284-015-1246-6