Abstract
Multiple sources of evidence show that the skuas (Aves:Stercorariidae) are a monophyletic group, closely related to gulls (Laridae. On morphological and behavioural evidence the Stercorariidae are divided into two widely divergent genera, Catharacta and Stercorarius, consistent with observed levels of nuclear and mitochondrial gene divergence. Catharacta skuas are large-bodied and with one exception breed in the Southern Hemisphere. Stercorarius skuas otherwise known as jaegers) are smaller bodied and breed exclusively in the Northern Hemisphere. Evidence from both mitochondrial and nuclear genomes and from ectoparasitic lice (Insecta:Phthiraptera) shows that the Pomarine skua, S. pomarinus, which has been recognized as being somewhat intermediate in certain morphological and behavioural characteristics, is much more closely related to species in the genus Catharacta, especially to the Northern Hemisphere-breeding Great skua, C. skua, than it is to the other two Stercorarius skuas, the Arctic skua, S. parasiticus and the Longtailed skua, S. longicaudus. Three possible explanations that might account for this discordant aspect of skua phylogeny are explored. These involve (i) the segregation of ancestral polymorphism, (ii) convergent evolution of morphology and behaviour or (iii) inter-generic hybridization. The available evidence from both nuclear and mitochondrial genomes does not exclude any of these hypotheses. Thus, resolution of this enigma of skua phylogeny awaits further work.
Full Text
The Full Text of this article is available as a PDF (308.2 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Allard M. W., Ellsworth D. L., Honeycutt R. L. The production of single-stranded DNA suitable for sequencing using the polymerase chain reaction. Biotechniques. 1991 Jan;10(1):24–26. [PubMed] [Google Scholar]
- Avise J. C., Neigel J. E., Arnold J. Demographic influences on mitochondrial DNA lineage survivorship in animal populations. J Mol Evol. 1984;20(2):99–105. doi: 10.1007/BF02257369. [DOI] [PubMed] [Google Scholar]
- Benson D. A., Boguski M., Lipman D. J., Ostell J. GenBank. Nucleic Acids Res. 1994 Sep;22(17):3441–3444. doi: 10.1093/nar/22.17.3441. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Desjardins P., Morais R. Sequence and gene organization of the chicken mitochondrial genome. A novel gene order in higher vertebrates. J Mol Biol. 1990 Apr 20;212(4):599–634. doi: 10.1016/0022-2836(90)90225-B. [DOI] [PubMed] [Google Scholar]
- Ellegren H. DNA typing of museum birds. Nature. 1991 Nov 14;354(6349):113–113. doi: 10.1038/354113a0. [DOI] [PubMed] [Google Scholar]
- Friesen V. L., Baker A. J., Piatt J. F. Phylogenetic relationships within the Alcidae (Charadriiformes: Aves) inferred from total molecular evidence. Mol Biol Evol. 1996 Feb;13(2):359–367. doi: 10.1093/oxfordjournals.molbev.a025595. [DOI] [PubMed] [Google Scholar]
- Grant P. R., Grant B. R. Hybridization of bird species. Science. 1992 Apr 10;256(5054):193–197. doi: 10.1126/science.256.5054.193. [DOI] [PubMed] [Google Scholar]
- Han C. Y., Lin B. K., Lin H. J. Methanol for preparing hair bulbs for PCR. Nucleic Acids Res. 1992 Dec 11;20(23):6419–6420. doi: 10.1093/nar/20.23.6419. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hedges S. B., Sibley C. G. Molecules vs. morphology in avian evolution: the case of the "pelecaniform" birds. Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):9861–9865. doi: 10.1073/pnas.91.21.9861. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kocher T. D., Thomas W. K., Meyer A., Edwards S. V., Päbo S., Villablanca F. X., Wilson A. C. Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers. Proc Natl Acad Sci U S A. 1989 Aug;86(16):6196–6200. doi: 10.1073/pnas.86.16.6196. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lansman R. A., Shade R. O., Shapira J. F., Avise J. C. The use of restriction endonucleases to measure mitochondrial DNA sequence relatedness in natural populations. III. Techniques and potential applications. J Mol Evol. 1981;17(4):214–226. doi: 10.1007/BF01732759. [DOI] [PubMed] [Google Scholar]
- Moum T., Johansen S., Erikstad K. E., Piatt J. F. Phylogeny and evolution of the auks (subfamily Alcinae) based on mitochondrial DNA sequences. Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):7912–7916. doi: 10.1073/pnas.91.17.7912. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Olsen G. J., Matsuda H., Hagstrom R., Overbeek R. fastDNAmL: a tool for construction of phylogenetic trees of DNA sequences using maximum likelihood. Comput Appl Biosci. 1994 Feb;10(1):41–48. doi: 10.1093/bioinformatics/10.1.41. [DOI] [PubMed] [Google Scholar]
- Richman A. D., Price T. Evolution of ecological differences in the Old World leaf warblers. Nature. 1992 Feb 27;355(6363):817–821. doi: 10.1038/355817a0. [DOI] [PubMed] [Google Scholar]
- Schnell G. D. A phenetic study of the suborder Lari (Aves). II. Phenograms, discussion, and conclusions. Syst Zool. 1970 Sep;19(3):264–302. [PubMed] [Google Scholar]
- Smith S. W., Overbeek R., Woese C. R., Gilbert W., Gillevet P. M. The genetic data environment an expandable GUI for multiple sequence analysis. Comput Appl Biosci. 1994 Dec;10(6):671–675. doi: 10.1093/bioinformatics/10.6.671. [DOI] [PubMed] [Google Scholar]
- Williams J. G., Kubelik A. R., Livak K. J., Rafalski J. A., Tingey S. V. DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Res. 1990 Nov 25;18(22):6531–6535. doi: 10.1093/nar/18.22.6531. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yu K., Pauls K. P. Optimization of the PCR program for RAPD analysis. Nucleic Acids Res. 1992 May 25;20(10):2606–2606. doi: 10.1093/nar/20.10.2606. [DOI] [PMC free article] [PubMed] [Google Scholar]