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Australian Journal of Zoology Australian Journal of Zoology Society
Evolutionary, molecular and comparative zoology
RESEARCH ARTICLE

Evolution and maintenance of colour pattern polymorphism in Liopholis (Squamata : Scincidae)

David G. Chapple A B G , Mark N. Hutchinson C , Brad Maryan D , Mike Plivelich E , Jennifer A. Moore F and J. Scott Keogh B
+ Author Affiliations
- Author Affiliations

A Museum Victoria, Division of Sciences, Herpetology Section, GPO Box 666, Melbourne, Vic. 3001, Australia.

B School of Botany and Zoology, Australian National University, Canberra, ACT 0200, Australia.

C South Australian Museum, Herpetology Section, Adelaide, SA 5000, Australia.

D Western Australian Museum, Terrestrial Vertebrates, Locked Bag 49, Welshpool DC, WA 6986, Australia.

E Ministry of Agriculture and Forestry, PO Box 2526, Wellington, New Zealand.

F Allan Wilson Centre for Molecular Ecology and Evolution, School of Biological Sciences, Victoria University of Wellington, PO Box 600, Wellington 6140, New Zealand.

G Corresponding author. Email: dchapple@museum.vic.gov.au

Australian Journal of Zoology 56(2) 103-115 https://doi.org/10.1071/ZO08040
Submitted: 18 April 2008  Accepted: 25 July 2008   Published: 13 October 2008

Abstract

We examined the evolution and maintenance of colour pattern polymorphism in an Australian lineage of scincid lizards, the genus Liopholis. Liopholis comprises 11 species, with representatives in both the temperate zone and arid zone. Specimens from all major Australian museums were examined to characterise colour pattern polymorphism within Liopholis, and investigate geographic variation in the relative abundance of morphs within polymorphic species. We used a previously published phylogeny for Liopholis to investigate the evolution and maintenance of colour pattern polymorphism within the group. Five species were found to exhibit colour pattern polymorphism (L. margaretae margaretae Storr, L. m. personata Storr, L. montana Donnellan et al., L. multiscutata Mitchell & Behrndt, L. pulchra Werner, L. whitii Lacépède), with six species being monomorphic (L. guthega Donnellan et al., L. inornata Rosén, L. kintorei Stirling & Zietz, L. modesta Storr, L. slateri Storr, L. striata Sternfeld). Three colour morphs occur in L. whitii, with the relative abundance of each varying significantly among latitudes. The patterned morph is most common, while the incidence of the plain-back morph decreases at latitudes higher than 35°S. The L. whitii patternless morph occurs only within a narrow latitudinal band (34–38°S). In L. multiscutata, the relative abundance of the patterned (~89–93%) and patternless morph (~7–11%) is consistent across regions, except for the Nullarbor Plain region where the patternless morph is more common (~39%). Our analyses suggest a single origin of colour pattern polymorphism in Liopholis, followed by the subsequent loss of polymorphism on four occasions. The secondary loss of polymorphism might be associated with climate or habitat, possibly as the result of shifts into the arid zone or alpine regions of Australia. This study provides the necessary framework for future studies of colour pattern polymorphism in Liopholis.


Acknowledgements

We thank S. Blomberg, N. Clemann, J. Cole, G. Fyfe, R. Henzell, P. Horner, D. Matthews, D. Milton, C. Pavey, G. Shea and A. Moussalli for providing information and/or useful discussions that greatly improved the manuscript. J. Melville, D. Bray, R. Sadlier, A. Amey, P. Couper, J. Wombey and R. Palmer provided access to museum collections. We thank N. Clemann (plain-back L. montana), P. Horner and G. Fyfe (patterned and patternless L. m. margaretae) for providing photos of colour morphs. Funding was provided to DGC from the following sources: Australian Geographic, Australian Society of Herpetologists (ASH), Student Research Grant, American Society of Ichthyologists and Herpetologists (ASIH) Gaige Fund Award, Society for Systematic Biologists (SSB) Award for Graduate Student Research, Joyce W. Vickery Scientific Research Fund (Linnean Society of NSW), Peter Rankin Trust Fund for Herpetology, and the Ecological Society of Australia (ESA) Student Research Grant. Financial support was also provided by a research grant from the Australian Research Council (ARC) to JSK.


References

Capula, M. , and Luiselli, L. (1994). Reproductive strategies in alpine adders, Vipera berus. The black females bear more often. Acta Oecologica 15, 207–214.
Henzell R. P. (1972). Adaptation to aridity in lizards of the Egernia whitei species-group. Ph.D. Thesis, University of Adelaide.

Hoekstra, H. E. , Drumm, K. E. , and Nachman, M. W. (2004). Ecological genetics of adaptive color polymorphism in pocket mice: geographic variation in selected and neutral genes. Evolution 58, 1329–1341.
CAS | PubMed | Horner P. (1991). ‘Skinks of the Northern Territory.’ (Northern Territory Museum of Arts and Sciences: Darwin.)

Hughes, J. M. , and Mather, P. B. (1986). Evidence for predation as a factor in determining shell color frequencies in a mangrove snail Littorina spp. (Prosobranchia: Littorinidae). Evolution 40, 68–77.
Crossref | GoogleScholarGoogle Scholar | Maddison D. R. , and Maddison W. P. (2000). ‘MacClade 4: Analysis of Phylogeny and Character Evolution.’ (Sinauer Associates: Sunderland, MA.)

Milton, D. (1990). Genetic evidence for sympatric differentiation between two colour morphs of the skink Egernia whitii. Australian Journal of Zoology 38, 117–130.
Crossref | GoogleScholarGoogle Scholar | Wilson S. , and Swan G. (2008). ‘A Complete Guide to Reptiles of Australia.’ 2nd edn. (Reed New Holland: Sydney.)