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Prickly forest skink

The prickly skink, or prickly forest skink, is a morphologically and genetically distinctive species of skink endemic to rainforests of the Wet Tropics of Queensland World Heritage Area, in north-eastern Australia. Unlike most small skinks, which have smooth scales, this species has rough, ridged and pointed scales. These keeled scales may be an adaptation to its high-rainfall habitat, to its microhabitat in rotting logs, or to camouflage it when moving through forest leaf-litter.

Taxonomy
This species is a member of the Australian "Sphenomorphid" group of skinks (family Scincidae), which includes such genera as Ctenotus, Anomalopus and Eulamprus. It is monotypic in the genus Gnypetoscincus. ==Distribution and life History==
Distribution and life History
The prickly skink is a habitat specialist restricted to closed canopy forest in high rainfall areas (rainforests) of the Australian Wet Tropics, extending from lowland tropical rainforest to montane forests on the adjacent hills and tablelands. Within these rainforests the prickly skink occurs within rotting logs and leaf litter and although locally abundant in some areas, it is rarely seen without searching. This species is ovoviviparous, and despite living in an equable climate, reproduction is seasonal, with females giving birth to 2-5 young in February - April. Animals mature at a snout-vent length (SVL) of around and grow to a maximum SVL of , with no obvious difference in external morphology or size between females and males. ==Phylogeography and Population Biology==
Phylogeography and Population Biology
Extensive upland areas of the Australian Wet Tropics, such as the Atherton Tableland, were cleared for farming, largely between 1940 and 1990, leaving many scattered pockets of rainforest surrounded by open pasture. The prickly skink is abundant throughout this area and has become a research subject for studies on the effect of habitat fragmentation on genetic diversity, gene flow and adaptation in a rainforest dependent species. A 1993 phylogeographic study by Moritz and co-authors using allozyme electrophoresis and restriction mapping of mitochondrial DNA (mtDNA) genomes found distinct genetic lineages in populations from the northern and southern wet tropics. These areas are currently connected by a ribbon of rainforest habitat, around wide, known as the Black Mountain Corridor or BMC, but historical climate modeling suggest that rainforests in the northern and southern wet tropics were separated by around of dry habitats in this area during Pleistocene glacial climate periods. The late-Pleistocene divergence between these lineages (>0.5% across the mtDNA genome) is an order of magnitude less than that between the Northern and Southern Wet Tropics but is indicative of emergence from separate glacial refugia. The larger Wooroonooran refugium maintained higher diversity through the glacial period than the southern Tableland refugium and this natural historical difference in genetic diversity is much greater than any more recent, human induced, effects of forest clearing and fragmentation. Also, Sumner found relatedness among males within fragments was lower in isolated forest fragments than within continuous forests, possibly reflecting greater dispersal within fragments due to lower habitat quality. However, these relatively slight differences show the difficulty of detecting effects of recent habitat fragmentation in a species with relatively low local population size and limited dispersal. Sumner and co-authors did find other ecological effects of fragmentation; skink abundance was higher in continuous forest sites than in fragments, and was lower in small habitat patches than in large patches, and on average, skinks from fragments were smaller than those from continuous forests. Estimates of population density and dispersal distances from capture-recapture methods and from genetic data are broadly consistent, with a density varying from 65 - 136 individuals per ha, and a dispersal distance of 404 – 843 m2, respectively. Genetic estimates of relatedness among individuals found under the same log revealed that juveniles tend to stay with their parents for 1–2 years and subsequently disperse to other logs, with marked individuals observed away from their initial capture site over three years. ==References==
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