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9 - Comparative ecomorphology and biogeography of Herpestidae and Viverridae (Carnivora) in Africa and Asia

Published online by Cambridge University Press:  05 July 2014

Gina D. Wesley-Hunt
Affiliation:
Montgomery College
Reihaneh Dehghani
Affiliation:
Stockholm University
Lars Werdelin
Affiliation:
Swedish Museum of Natural History
Anjali Goswami
Affiliation:
University College London
Anthony Friscia
Affiliation:
University of California, Los Angeles
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Summary

Introduction

Ecological morphology (ecomorphology) is a powerful tool for exploring diversity, ecology, and evolution in concert (Wainwright, 1994, and references therein). Alpha taxonomy and diversity measures based on taxon counting are the most commonly used tools for understanding long-term evolutionary patterns and provide the foundation for all other biological studies above the organismal level. However, this provides insight into only a single dimension of a multidimensional system. As a complement, ecomorphology allows us to describe the diversification and evolution of organisms in terms of their morphology and ecological role. This is accomplished by using quantitative and semi-quantitative characterisation of features of organisms that are important, for example, in niche partitioning or resource utilisation. In this context, diversity is commonly referred to as disparity (Foote, 1993). The process of speciation, for example, can be better understood and hypotheses more rigorously tested if it can be quantitatively demonstrated whether a new species looks very similar to the original taxon or whether its morphology has changed in a specific direction. For example, if a new species of herbivore evolves with increased grinding area in the cheek dentition, it can either occupy the same area of morphospace as previously existing species, suggesting increased resource competition, or it can occupy an area of morphospace that had previously been empty, suggesting evolution into a new niche. This example illustrates a situation where speciation did not just increase the number of taxa, but also morphologic and ecologic diversity. In turn, this quantitative information can be used to test speciation hypotheses in the extant fauna as well as the fossil record suggested by previous studies using molecular data and habitat reconstruction (Gaubert and Begg, 2007).

Type
Chapter
Information
Carnivoran Evolution
New Views on Phylogeny, Form and Function
, pp. 246 - 268
Publisher: Cambridge University Press
Print publication year: 2010

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References

Damuth, J. D. (1992). Taxon-free characterization of animal communities. In Terrestrial Ecosystems through Time, ed. Behrensmeyer, A. K., Damuth, J. D., DiMichele, W. A., Potts, R., Sues, H.-D. and Wing, S. L.. Chicago, IL:University of Chicago Press, pp. 183–203.Google Scholar
Damuth, J. and MacFadden, B. J., eds. (1990). Body Size in Mammalian Paleobiology: Estimation and Biological Implications. Cambridge: Cambridge University Press, 397.Google Scholar
Flynn, J. J. and Nedbal, M. A. (1998). Phylogeny of the Carnivora (Mammalia): congruence vs incompatibility among multiple data sets. Molecular Phylogenetics and Evolution, 9, 414–26.CrossRefGoogle ScholarPubMed
Flynn, J. J., Finarelli, J. A., Zehr, S., Hsu, J. and Nedbal, M. A. (2005). Molecular phylogeny in the Carnivora (Mammalia): assessing the impact of increased sampling on resolving enigmatic relationships. Systematic Biology, 54, 317–37.CrossRefGoogle ScholarPubMed
Foote, M. (1993). Contributions of individual taxa to overall morphological disparity. Paleobiology, 19, 403–19.CrossRefGoogle Scholar
Foote, M. (1994). Morphological disparity in Ordovician–Devonian crinoids and the early saturation of morphological space. Paleobiology, 20, 320–44.CrossRefGoogle Scholar
Foote, M. (1997). The evolution of morphological diversity. Annual Review of Ecology and Systematics, 28, 129–52.CrossRefGoogle Scholar
Friscia, A. R., Van Valkenburgh, B. and Biknevicius, A. R. (2007). An ecological analysis of extant small carnivorans. Journal of Zoology, 272, 82–100.CrossRefGoogle Scholar
Gaubert, P. and Begg, C. M. (2007). Re-assessed molecular phylogeny and evolutionary scenario within genets (Carnivora, Viverridae, Genettinae). Molecular Phylogenetics and Evolution, 44, 920–27.CrossRefGoogle Scholar
Gaubert, P. and Cordeiro-Estrela, P. (2006). Phylogenetic systematics and tempo of evolution of the Viverrinae (Mammalia, Carnivora, Viverridae) within feliformians: implications for faunal exchanges between Asia and Africa. Molecular Phylogenetics and Evolution, 41, 266–78.CrossRefGoogle ScholarPubMed
Gaubert, P. and Veron, G. (2003). Exhaustive sample set among Viverridae reveals the sister-group of felids: the linsangs as a case of extreme morphological convergence within Feliformia. Proceedings of the Royal Society, London Series B, 270, 2523–30.CrossRefGoogle ScholarPubMed
Gaubert, P., Veron, G. and Tranier, M. (2002). Genets and ‘genet-like’ taxa (Carnivora, Viverrinae): phylogenetic analysis, systematics and biogeographic implications. Zoological Journal of the Linnean Society, 134, 317–34.CrossRefGoogle Scholar
Gaubert, P., Fernandes, C. A., Bruford, M. W. and Veron, G. (2004a). Genets (Carnivora, Viverridae) in Africa: an evolutionary synthesis based on cytochrome b sequences and morphological characters. Biological Journal of the Linnean Society, 81, 589–610.CrossRefGoogle Scholar
Gaubert, P., Tranier, M., Delmas, A.-S., Colyn, M. and Veron, G. (2004b). First molecular evidence for reassessing phylogenetic affinities between genets (Genetta) and the enigmatic genet-like taxa Osbornictis, Poiana, and Prionodon (Carnivora, Viverridae). Zoologica Scripta, 32, 117–29.CrossRefGoogle Scholar
Gaubert, P., Wozencraft, W. C., Cordeiro-Estrela, P. and Veron, G. (2005). Mosaics of convergences and noise in morphological phylogeneties: what's in a viverrid-like carnivoran?Systematic Biology, 54, 865–94.CrossRefGoogle Scholar
Gregory, W. K. and Hellman, M. (1939). On the evolution and major classification of the civets (Viverridae) and allied fossil and recent Carnivora: a phylogenetic study of the skull and dentition. Proceedings of the American Philosophical Society, 81, 309–92.Google Scholar
Hunt, R. M.. (1974). The auditory bulla in Carnivora: an anatomical basis for reappraisal of carnivore evolution. Journal of Morphology, 143, 21–76.CrossRefGoogle ScholarPubMed
Hunt, R. M.. (1996). Basicranial anatomy of the giant viverrid from ‘E’ Quarry, Langebaanweg, South Africa. In Palaeoecology and Palaeoenvironments of Late Cenozoic Mammals: Tributes to the Career of C. S. (Rufus) Churcher, ed. Stewart, K. M. and Seymour, K. L.. Toronto: University of Toronto Press, pp. 588–97.Google Scholar
Kretzoi, M. and Fejfar, O. (1982). Viverriden (Carnivora, Mammalia) im europäischen Altpleistozän. Zeitschrift für geologische Wissenschaften, 10, 979–95.Google Scholar
Lupia, R. (1999). Discordant morphological disparity and taxonomic diversity during the Cretaceous angiosperm radiation: North American pollen record. Paleobiology, 25, 1–28.Google Scholar
Owen-Smith, R. N. (1988). Megaherbivores: The Influence of Very Large Body Size on Ecology. Cambridge: Cambridge University Press, 369 pp.CrossRefGoogle Scholar
Patou, M.-L., Debruyne, R., Jennings, A., Zubaid, A., Rovie-Ryan, J. J. and Veron, G. (2008). Phylogenetic relationships of the Asian palm civets (Hemigalinae & Paradoxurinae, Viverridae, Carnivora). Molecular Phylogenetics and Evolution, 47, 883–92.CrossRefGoogle Scholar
Perez, M., Li, B., Tillier, A., Cruaud, A., and Veron, G. (2006). Systematic relationships of the bushy-tailed and black-footed mongooses (genus Bdeogale, Herpestidae, Carnivora) based on molecular, chromosomal and morphological evidence. Journal of Zoological Systematics, 44, 251–59.CrossRefGoogle Scholar
Radinsky, L. B. (1981a). Evolution of skull shape in carnivores 1. Representative modern carnivores. Biological Journal of the Linnean Society, 15, 369–88.CrossRefGoogle Scholar
Radinsky, L. B. (1981b). Evolution of skull shape in carnivores 2. Additional modern carnivores. Biological Journal of the Linnean Society, 16, 337–55.CrossRefGoogle Scholar
Radinsky, L. B. (1982). Evolution of skull shape in carnivores. 3. The origin and early radiation of the modern carnivore families. Paleobiology, 8(3), 177–95.CrossRefGoogle Scholar
Ray, J. C. (1995). Civettictis civetta. Mammalian Species, 488, 1–7.CrossRefGoogle Scholar
Van Valkenburgh, B. (1988). Trophic diversity in past and present guilds of large predatory mammals. Paleobiology, 14, 155–73.CrossRefGoogle Scholar
Van Valkenburgh, B. (1989). Carnivore dental adaptations and diet: a study of trophic diversity within guilds. In Carnivore Behavior, Ecology and Evolution, ed. Gittleman, J. L.. Ithaca, NY: Cornell University Press, pp. 410–36.CrossRefGoogle Scholar
Veron, G. and Catzeflis, F. M. (1993). Phylogenetic relationships of the endemic Malagasy carnivore Cryptoprocta ferox (Aeluruidea): DNA/DNA hybridization experiments. Journal of Mammalian Evolution, 1, 169–85.CrossRefGoogle Scholar
Veron, G. and Heard, S. (2000). Molecular systematics of the Asiatic Viverridae (Carnivora) inferred from mitochondrial cytochrome b sequence analysis. Journal of Zoological Systematics and Evolutionary Research, 38, 209–17.CrossRefGoogle Scholar
Veron, G., Colyn, M., Dunham, A. E., Taylor, P. and Gaubert, P. (2004). Molecular systematics and origin of sociality in mongooses (Herpestidae, Carnivora). Molecular Phylogenetics and Evolution, 30, 582–98.CrossRefGoogle Scholar
Wainwright, P. C. (1994). Functional morphology as a tool in ecological research. In Ecological Morphology: Integrative Organismal Biology, ed. Wainwright, P. C. and Reilly, S. M.. Chicago, IL: The University of Chicago Press, pp. 42–59.Google Scholar
Werdelin, L. (1996). Carnivoran ecomorphology: a phylogenetic perspective. In Carnivore Behavior, Ecology, and Evolution. Volume 2, ed. Gittleman, J. L.. Ithaca, NY: Cornell University Press, pp. 582–624.Google Scholar
Werdelin, L. (2003). Mio-Pliocene Carnivora from Lothagam, Kenya. In Lothagam: The Dawn of Humanity in Eastern Africa, ed. Leakey, M. G. and Harris, J. M.. New York, NY: Columbia University Press, pp. 261–314.Google Scholar
Werdelin, L. and Lewis, M. E. (2005). Plio-Pleistocene Carnivora of eastern Africa: species richness and turnover patterns. Zoological Journal of the Linnean Society, 144, 121–44.CrossRefGoogle Scholar
Werdelin, L. and Peigné, S. (2010). Carnivora. In Cenozoic Mammals of Africa, ed. Werdelin, L. and Sanders, W. J.. Berkeley, CA: University of California Press, pp. 609–63.CrossRefGoogle Scholar
Wesley-Hunt, G. D. (2005). The morphological diversification of carnivores in North America. Paleobiology, 31, 35–55.2.0.CO;2>CrossRefGoogle Scholar
Wozencraft, W. C. (1993). Order Carnivora. In Mammal Species of the World — A Taxonomic and Geographic Reference, ed. Wilson, D. E. and Reeder, D. M.. Washington, DC: Smithsonian Institution Press, pp. 279–348.Google Scholar
Yoder, A. D., Burns, M. M., Zehr, S., et al. (2003). Single origin of Malagasy Carnivora from an African ancestor. Nature, 421, 734–37.CrossRefGoogle ScholarPubMed

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