Mniarogekko, Bauer, Aaron M., Jackman, Todd R., Sadlier, Ross A. & Whitaker, Anthony H., 2012
publication ID |
https://doi.org/10.5281/zenodo.211734 |
DOI |
https://doi.org/10.5281/zenodo.6166582 |
persistent identifier |
https://treatment.plazi.org/id/5C4F87E1-FFA1-FFB9-088F-FDC6D653B32E |
treatment provided by |
Plazi (2016-04-12 23:05:42, last updated 2023-10-26 17:41:39) |
scientific name |
Mniarogekko |
status |
gen. nov. |
Mniarogekko gen. nov.
Mniarogekko chahoua — No subspecies have been described and no synonyms exist for Mniarogekko chahoua , nor have previous authors discussed intraspecific variation in the context of possible taxonomic significance. However, our results reveal relatively large intraspecific divergence within this taxon ( Figs. 1–2 View FIGURE 1 View FIGURE 2 ). Seipp and Henkel (2000) first noted that M. chahoua occurred in far northern New Caledonia, northeast of Koumac, and speculated that the species might be distributed island-wide. Specimens from this same population, at Rivière Néhoué, were reported on extensively by Langner (2009). Mniarogekko chahoua specimens from recently discovered northern populations on Île Art in the Belep group and at Vallée Poupoule, Dôme de Tiébaghi, and Rivière Néhoué in the far northwest of the Grande Terre ( Whitaker et al. 2004; Bauer et al. 2006b) are morphologically similar to one another but 7.8% divergent with respect to more southern Grande Terre specimens from Sarraméa and the Vallée d’Amoa. Specimens from these latter two localities are likewise highly genetically divergent from one another, but existing sample sizes are small and morphological differences between them have not yet been identified. All northern samples come from ultramafic areas, whereas those from the east-central and more southern Grande Terre populations are from low elevation (vallicole) habitats on non-ultramafic substrates ( Fig. 17 View FIGURE 17 ). Bauer (1985) reviewed M. chahoua , then known from very few specimens, and designated a specimen from the Vallée d’Amoa as the neotype (many captive M. chahoua supposedly derive from Île des Pins stock and these are stated by herpetoculturalists to differ from Grande Terre M. chahoua ; however, we have not encountered Mniarogekko on the Île des Pins and have not examined museum specimens from this locality, therefore, we are unable to evaluate their taxonomic status). We believe that genetic and morphological differences warrant the description of a second chahoua -like species to accommodate the northern populations sampled here. This is described below:
Bauer, A. M. (1985) Notes on the taxonomy, morphology and behaviour of Rhacodactylus chahoua (Bavay) (Reptilia: Gekkonidae). Bonner zoologische Beitrage, 36, 81 - 94
Bauer, A. M., Jackman, T., Sadlier, R. A. & Whitaker, A. H. (2006 b) A revision of the Bavayia validiclavis group (Squamata: Gekkota: Diplodactylidae), a clade of New Caledonian geckos exhibiting microendemism. Proceedings of the California Academy of Sciences, 57, 503 - 547.
Langner, C. (2009) Der Neukaledonische Flechtengecko, Rhacodactylus chahoua. Draco, 9 (4), 64 - 71.
Seipp, R. & Henkel, F. - W. (2000) Rhacodactylus: Biology, Natural History and Husbandry. Edition Chimaira, Frankfurt am Main, 173 pp.
Whitaker, A. H., Sadlier, R. A., Bauer, A. M. & Whitaker, V. A. (2004) Biodiversity and conservation status of lizards in threatened and restricted habitats of north-western New Caledonia. Unpublished report by Whitaker Consultants Limited to Direction du Developpement Economique et de l'Environnement, Province Nord, Kone, New Caledonia, viii + 106 pp.
FIGURE 1. Maximum likelihood tree based on the mitochondrial ND 2 gene and flanking tRNAs showing relationships among species of New Caledonian diplodactylids and their immediate sister-group, the Australian genus Pseudothecadactylus. Values subtending branches are maximum likelihood / Bayesian posterior probabilities above the line and maximum parsimony bootstrap values below the line. Dashes for posterior probabilities indicate no support for the maximum likelihood topology whereas dashes for maximum parsimony bootstraps indicates values <50 %. Support values are not shown for conspecific relationships where samples differ by three or fewer bases. In the case of Rhacodactylus auriculatus southern ultramafic block samples are cumulatively represented as a triangle.
FIGURE 2. Maximum likelihood tree based on the combined mitochondrial (ND 2 and flanking tRNAs) and nuclear genes (RAG 1) showing relationships among species of New Caledonian diplodactylids and their immediate sister-group, the Australian genus Pseudothecadactylus. The tree has been pruned to show only one exemplar for each taxon. Both intra- and interspecific patterns of relationship are nearly identical to those supported by ND 2 only (Fig. 1). Only within Dierogekko and Rhacodactylus sensu stricto are alternative patterns hypothesized (see text). Values subtending branches are maximum likelihood / Bayesian posterior probabilities above the line and maximum parsimony bootstrap values below the line. Dashes for posterior probabilities indicate no support for the maximum likelihood topology whereas dashes for maximum parsimony bootstraps indicates values <50 %.
FIGURE 17. Distribution map of Mniarogekko chahoua (green symbols) and M. jalu sp. nov. (red symbols). Type localities are marked by stars. The question mark on the Île des Pins represents numerous literature records for M. chahoua that lack precise locality data. See Appendix for a list of localities mapped.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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