Published May 5, 2021 | Version v1
Taxonomic treatment Open

Hemiglyphidodontini Whitley 1929

Description

Tribe Hemiglyphidodontini.

This group consists of several well-established genera, a couple of monotypic genera, and a clade containing the only damselfishes that lack a pelagic larval stage. Even though it was not named as such, the existence of a clade with some combination of these component genera (Acanthochromis, Altrichthys, Amblyglyphidodon, Hemiglyphidodon, and Neoglyphidodon) is consistently supported across other phylogenetic studies (e.g., Quenouille et al., 2004; Cooper et al., 2009; Cowman and Bellwood, 2011; Litsios et al., 2012a, 2012b; Frédérich et al., 2013; Rabosky et al., 2013, 2018; Lobato et al., 2014; DiBattista et al., 2016; Mirande, 2016; Gaboriau et al., 2018; Delrieu-Trottin et al., 2019).

Notes

Published as part of Tang, Kevin L., Stiassny, Melanie L. J., Mayden, Richard L. & DeSalle, Robert, 2021, Systematics of Damselfishes, pp. 258-318 in Ichthyology & Herpetology 109 (1) on page 293, DOI: 10.1643/i2020105, http://zenodo.org/record/7846738

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Linked records

Additional details

Biodiversity

Family
Pomacentridae
Kingdom
Animalia
Order
Perciformes
Phylum
Chordata
Scientific name authorship
Whitley
Taxon rank
tribe
Taxonomic concept label
Hemiglyphidodontini Whitley, 1929 sec. Tang, Stiassny, Mayden & DeSalle, 2021

References

  • Quenouille, B., E. Bermingham, and S. Planes. 2004. Molecular systematics of the damselfishes (Teleostei: Pomacentridae): Bayesian phylogenetic analyses of mitochondrial and nuclear DNA sequences. Molecular Phylogenetics and Evolution 31: 66 - 88.
  • Litsios, G., C. A. Sims, R. O. Wuest, P. B. Pearman, N. E. Zimmermann, and N. Salamin. 2012 a. Mutualism with sea anemones triggered the adaptive radiation of clownfishes. BMC Evolutionary Biology 12: 212.
  • Litsios, G., L. Pellissier, F. Forest, C. Lexer, P. B. Pearman, N. E. Zimmermann, and N. Salamin. 2012 b. Trophic specialization influences the rate of environmental niche evolution in damselfishes (Pomacentridae). Proceedings of the Royal Society B: Biological Sciences 279: 3662 - 3669.
  • Frederich, B., L. Sorenson, F. Santini, G. J. Slater, and M. E. Alfaro. 2013. Iterative ecological radiation and convergence during the evolutionary history of damselfishes (Pomacentridae). The American Naturalist 181: 94 - 113.
  • Rabosky, D. L., F. Santini, J. Eastman, S. A. Smith, B. Sidlauskas, J. Chang, and M. E. Alfaro. 2013. Rates of speciation and morphological evolution are correlated across the largest vertebrate radiation. Nature Communications 4: 1958.
  • Rabosky, D. L., J. Chang, P. O. Title, P. F. Cowman, L. Sallan, M. Friedman, K. Kaschner, C. Garilao, T. J. Near, M. Coll, and M. E. Alfaro. 2018. An inverse latitudinal gradient in speciation rate for marine fishes. Nature 559: 392 - 395.
  • Lobato, F. L., D. R. Barneche, A. C. Siqueira, A. M. R. Liedke, A. Lindner, M. R. Pie, D. R. Bellwood, and S. R. Floeter. 2014. Diet and diversification in the evolution of coral reef fishes. PLoS ONE 9: e 102094.
  • Mirande, J. M. 2016. Combined phylogeny of ray-finned fishes (Actinopterygii) and the use of morphological characters in large-scale analyses. Cladistics 33: 333 - 350.
  • Gaboriau, T., F. Leprieur, D. Mouillot, and N. Hubert. 2018. Influence of the geography of speciation on current patterns of coral reef fish biodiversity across the Indo-Pacific. Ecography 41: 1295 - 1306.