| BMC Evolutionary Biology | |
| A multi-locus species phylogeny of African forest duikers in the subfamily Cephalophinae: evidence for a recent radiation in the Pleistocene | |
| Nicola M Anthony1  Anne R Johnston1  | |
| [1] University of New Orleans, New Orleans, LA, 70148, USA | |
| 关键词: Species tree; Partition; Molecular clock; Speciation; Pleistocene refuge hypothesis; Duiker; | |
| Others : 1140778 DOI : 10.1186/1471-2148-12-120 |
|
| received in 2011-12-23, accepted in 2012-07-05, 发布年份 2012 | |
PDF
|
|
【 摘 要 】
Background
Duikers in the subfamily Cephalophinae are a group of tropical forest mammals believed to have first originated during the late Miocene. However, knowledge of phylogenetic relationships, pattern and timing of their subsequent radiation is poorly understood. Here we present the first multi-locus phylogeny of this threatened group of tropical artiodactyls and use a Bayesian uncorrelated molecular clock to estimate divergence times.
Results
A total of 4152 bp of sequence data was obtained from two mitochondrial genes and four nuclear introns. Phylogenies were estimated using maximum parsimony, maximum likelihood, and Bayesian analysis of concatenated mitochondrial, nuclear and combined datasets. A relaxed molecular clock with two fossil calibration points was used to estimate divergence times. The first was based on the age of the split between the two oldest subfamilies within the Bovidae whereas the second was based on the earliest known fossil appearance of the Cephalophinae and molecular divergence time estimates for the oldest lineages within this group. Findings indicate strong support for four major lineages within the subfamily, all of which date to the late Miocene/early Pliocene. The first of these to diverge was the dwarf duiker genus Philantomba, followed by the giant, eastern and western red duiker lineages, all within the genus Cephalophus. While these results uphold the recognition of Philantomba, they do not support the monotypic savanna-specialist genus Sylvicapra, which as sister to the giant duikers leaves Cephalophus paraphyletic. BEAST analyses indicate that most sister species pairs originated during the Pleistocene, suggesting that repeated glacial cycling may have played an important role in the recent diversification of this group. Furthermore, several red duiker sister species pairs appear to be either paraphyletic (C.callipygus/C. ogilbyi and C. harveyi/C. natalensis) or exhibit evidence of mitochondrial admixture (C. nigrifrons and C. rufilatus), consistent with their recent divergence and/or possible hybridization with each other.
Conclusions
Molecular phylogenetic analyses suggest that Pleistocene-era climatic oscillations have played an important role in the speciation of this largely forest-dwelling group. Our results also reveal the most well supported species phylogeny for the subfamily to date, but also highlight several areas of inconsistency between our current understanding of duiker taxonomy and the evolutionary relationships depicted here. These findings may therefore prove particularly relevant to future conservation efforts, given that many species are presently regulated under the Convention for Trade in Endangered Species.
【 授权许可】
2012 Johnston and Anthony; licensee BioMed Central Ltd.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 20150325105718588.pdf | 2349KB | ||
| Figure 7. | 57KB | Image | |
| Figure 6. | 44KB | Image | |
| Figure 5. | 39KB | Image | |
| Figure 4. | 38KB | Image | |
| Figure 3. | 39KB | Image | |
| Figure 2. | 39KB | Image | |
| Figure 1. | 39KB | Image |
【 图 表 】
Figure 1.
Figure 2.
Figure 3.
Figure 4.
Figure 5.
Figure 6.
Figure 7.
【 参考文献 】
- [1]Haffer J: Alternative models of vertebrate speciation in Amazonia: an overview. Biodivers Conserv 1997, 6:451-476.
- [2]Da Silva M, Patton J: Molecular phylogeography and the evolution and conservation of Amazonian mammals. Mol Ecol 1998, 7:475-486.
- [3]Hewitt G: The structure of biodiversity - insights from molecular phylogeography. Front Zool 2004, 1:4.
- [4]Haffer J: Speciation in Amazonian forest birds. Sci New York 1969, 165:131-137.
- [5]Colinvaux P, De Oliveira P, Bush M: Amazonian and neotropical plant communities on glacial time-scales: the failure of the aridity and refuge hypotheses. Quat Sci Rev 2000, 19:141-169.
- [6]Willis K: Paleocology: the refugial debate. Sci. 2000, 287:1406-1407.
- [7]Lessa E, Cook J, Patton J: Genetic footprints of demographic expansion in North America, but not Amazonia, during the Late Quaternary. Proc Natl Acad Sci USA 2003, 100:10331-10334.
- [8]Querouil S, Verheyen E, Dillen M, Colyn M: Patterns of diversification in two African forest shrews: Sylvisorex johnstoni and Sylvisorex ollula (Soricidae, Insectivora) in relation to paleo-environmental changes. Mol Phylogenet Evol 2003, 28:24-37.
- [9]Plana V: Mechanisms and tempo of evolution in the African Guineo-Congolian rainforest. Philos. Trans R Soc Lond Ser B Biol Sci 2004, 359:1585-1594.
- [10]Bowie R, Fjeldså J, Hackett S, Bates J, Crowe T: Coalescent models reveal the relative roles of ancestral polymorphism, vicariance, and dispersal in shaping phylogeographical structure of an African montane forest robin. Mol Phylogenet Evolution 2006, 38:171-188.
- [11]Born C, et al.: Insights into the biogeographical history of the Lower Guinea Forest Domain: evidence for the role of refugia in the intraspecific differentiation of Aucoumea klaineana. Mol Ecol 2011, 20:131-142.
- [12]Nicolas V, et al.: The roles of rivers and Pleistocene refugia in shaping genetic diversity in Praomys misonnei in tropical Africa. J Biogeogr 2011, 38:191-207.
- [13]Anthony NM, et al.: The role of Pleistocene refugia and rivers in shaping gorilla genetic diversity in central Africa. Proc Natl Acad Sci USA 2007, 104:20432-20436.
- [14]Trauth M, Larrasoana J, Mudelsee M: Trends, rhythms and events in Plio-Pleistocene African climate. Quat Sci Rev 2009, 28:399-411.
- [15]Moodley Y, Bruford M: Molecular biogeography: towards an integrated framework for conserving pan-African biodiversity. PLoS One 2007, 2:454.
- [16]Brown D, et al.: Extensive population genetic structure in the giraffe. BMC Biol 2007, 5:57.
- [17]Janssens S, Fischer E, Stevart T: New insights into the origin of two new epiphytic Impatiens species (Balsaminaceae) from West Central Africa based on molecular phylogenetic analyses. Taxon 2010, 59:1508-1518.
- [18]Couvreur T, Chatrou L, Sosef M, Richardson J: Molecular phylogenetics reveal multiple tertiary vicariance origins of the African rain forest trees. BMC Biol 2008, 6:54.
- [19]Holstein N, Renner S: A dated phylogeny and collection records reveal repeated biome shifts in the African genus Coccinia (Cucurbitaceae). BMC Evol Biol 2011, 11:28.
- [20]Tolley K, et al.: Ancient forest fragmentation or recent radiation? Testing refugial speciation models in chameleons within an African biodiversity hotspot. J Biogeogr 2011, 38:1748-1760.
- [21]Vrba E: The fossil record of African antelopes (Mammalia, Bovidae) in relation to human evolution and paleoclimate. In Paleoclimate and evolution, with emphasis on human origins. Edited by Vrba E, Denton G, Partridge T, Burckle L. Yale University Press, New Haven; 1995:385-424.
- [22]Jansen van Vuuren Vuuren B, Robinson T: Retrieval of four adaptive lineages in duiker antelope: evidence from mitochondrial DNA sequences and fluorescence in situ hybridization. Mol Phylogenet Evol 2001, 20:409-425.
- [23]Ntie S, et al.: A molecular diagnostic for identifying central African forest artiodactyls from faecal pellets. Anim Conserv 2010, 13:80-93.
- [24]Johnston A, Morikawa M, Ntie S, Anthony N: Evaluating DNA barcoding criteria using African duiker antelope (Cephalophinae) as a test case. Conserv Genet 2011, 12:1173-1182.
- [25]Matthee C, Davis S: Molecular insights into the evolution of the family Bovidae: a nuclear DNA perspective. Mol Biol Evol 2001, 18:1220-1230.
- [26]Willows-Munro S, Robinson T, Matthee C: Utility of nuclear DNA intron markers at lower taxonomic levels: phylogenetic resolution among nine Tragelaphus spp. Mol Phylogenet Evol 2005, 35:624-636.
- [27]Drummond A, Ho S, Phillips M, Rambaut A: Relaxed phylogenetics and dating with confidence. Plos Biol. 2006, 4:699-710.
- [28]Grubb P: Patterns of speciation in African Mammals. Bull Carnegie Mus Nat Hist 1978, 6:152-165.
- [29]Funk D, Omland K: Species-level paraphyly and polyphyly: frequency, causes, and consequences, with insights from animal mitochondrial DNA. Annu Rev Ecol Evol Syst 2003, 34:397-423.
- [30]Zink R, Barrowclough G: Mitochondrial DNA under siege in avian phylogeography. Mol Ecol 2008, 17:2107-2121.
- [31]Zachos J, Pagani M, Sloan L, Thomas E, Billups K: Trends, rhythms and aberrations in global climate 65 Ma to present. Sci. 2001, 292:686-693.
- [32]deMenocal P: Plio-Pleistocene African Climate. Sci 1995, 270:53-59.
- [33]van Zinderen Bakker E, Mercer H: Major late cainozoic climate events and paleoenvironmental changes in Africa viewed in a worldwide context. Paleogeogr Paleoclimatol Paleoecol 1986, 56:217-235.
- [34]Hamilton A, Taylor D: History of climate and forests in tropical Africa during the last 8 million years. Clim Chang 1991, 19:65-78.
- [35]Maley J: The African rainforest – main characteristics of changes in vegetation and climate from the upper cretaceous to the quaternary. Proc R Soc Edinb 1996, 104N:31-73.
- [36]Prance G: A review of the phytogeographic evidence for Pleistocene climate change in the neotropics. Ann Mo Bot Gar 1982, 69:594-624.
- [37]Moritz C, Patton J, Schneider C, Smith T: Diversification of rainforest faunas: an integrated molecular approach. Annu Rev Ecol Syst 2000, 31:533-563.
- [38]Fjelds J: Geographical patterns for relict and young species of birds in Africa and South America and implications for conservation priorities. Biodivers Conserv 1994, 3:207-226.
- [39]Aduse-Poku K, Vingerhoedt E, Wahlberg N: Out-of-Africa again: a phylogenetic hypothesis of the genus Charaxes (Lepidoptera: Nymphalidae) based on five gene regions. Mol Phylogenet Evol 2009, 53:463-478.
- [40]Alpers D, Jansen van Vuuren B, Arctander P, et al.: Population genetics of the roan antelope (Hippotragus equinus) with suggestions for conservation. Mol Ecol 2004, 13:1771-1784.
- [41]Nicolas V, Missoup A, Denys C, et al.: The roles of rivers and Pleistocene refugia in shaping genetic diversity in Praomys misonnei in tropical Africa. J Biogeogr 2011, 38:191-207.
- [42]Thalmann O, Fischer A, Lankester F, Pääbo S, Vigilant L: The complex evolutionary history of gorillas: insights from genomic DNA. Mol Biol Evol 2007, 24:146-158.
- [43]Avise J, Walker D, Johns G: Speciation durations and Pleistocene effects on vertebrate phylogeography. Proc R Soc Lond Ser B-Biol Sci 1998, 265:1707-1712.
- [44]Hey J: Isolation with migration models for more than two populations. Mol Biol Evol 2010, 27:905-920.
- [45]Crandall K, Bininda-Emonds O, Mace G, Wayne R: Considering evolutionary processes in conservation biology. Trends Ecol Evol 2000, 15:290-295.
- [46]Kingdon J: The Kingdon Field Guide to African Mammals. New York and London, Academic Press; 1997.
- [47]Eaton M, et al.: Barcoding bushmeat: molecular identification of Central African and South American harvested vertebrates. Conserv Genet 2009, 11:1389-1404.
- [48]Hamilton A, Taylor D: History of climate and forests in tropical Africa during the last 8 million years. Clim Change 1991, 19:65-78.
- [49]Damm S, Dijkstra K, Hadrys H: Red drifters and dark residents: the phylogeny and ecology of a Plio-Pleistocene dragonfly radiation reflects Africa’s changing environment (Odonata, Libellulidae, Trithemis). Mol Phylogenet Evol 2010, 54:870-82.
- [50]Voelker G, Outlaw R, Bowie R: Pliocene forest dynamics as a primary driver of African bird speciation. Global Ecol and Biogeogr 2010, 19:111-121.
- [51]: IUCN 2011. IUCN Red List of Threatened Species. Version 2011.2. , ; . http://www.iucnredlist.org. Downloaded on 5 August 2011
- [52]Colyn M, et al.: Discovery of a new duiker species (Bovidae: Cephalophinae) from the Dahomey Gap. West Africa Zootaxa 2010, 2637:1-30.
- [53]Hassanin A, Douzery E: The tribal radiation of the family Bovidae (Artiodactyla) and the evolution of the mitochondrial cytochrome b gene. Mol Phylogenet Evol 1999, 13:227-243.
- [54]Agnarsson I, May-Collado L: The phylogeny of Cetartiodactyla: the importance of dense taxon sampling, missing data, and the remarkable promise of cytochrome b to provide reliable species-level phylogenies. Mol Phylogenet Evol 2008, 48:964-985.
- [55]Hernandez Fernandez M, Vrba E: A complete estimate of the phylogenetic relationships in Ruminantia: a dated species-level supertree of the extant ruminants. Biol Rev (Cambridge) 2005, 80:269-302.
- [56]Bowkett A, Rovero F, Marshall A: The use of camera-trap data to model habitat use by antelope species in the Udzungwa mountain forests, Tanzania. Afr J Ecol 2008, 46:479-487.
- [57]Sambrook J, Russell D: Molecular cloning: A Laboratory Manual. Cold Springs Harbor Laboratory Press, Cold Springs Harbor; 2001.
- [58]Aljanabi S, Martinez I: Universal and rapid salt-extraction of high quality genomic DNA for PCR-based techniques. Nucleic Acid Res 1997, 25:4692-4693.
- [59]Matthee C, Robinson T: Cytochrome b phylogeny of the family bovidae: Resolution within the Alcelaphini, Antilopini, Neotragini, and Tragelaphini. Mol Phylogenet Evol 1999, 12:31-46.
- [60]Kumar S, Tamura K, Nei M: MEGA: integrated software for molecular evolutionary genetics analysis and sequence alignment. Briefings Bioinform 2004, 5:150-163.
- [61]Matthee C, Burzlaff J, Taylor J, Davis S: Mining the mammalian genome for artiodactyl systematics. Syst Biol 2001, 50:367-390.
- [62]Glenn T, Schable N: Isolating microsatellite DNA loci. In Molecular Evolution: Producing the Biochemical Data, Part B. Elsevier Academic Press Inc, San Diego; 2005.
- [63]Farris J, et al.: Constrcting a significance test for incongruence. Syst Biol 1995, 44:570-572.
- [64]Swofford D: PAUP*: phylogenetics analysis using parsimony (*and other mothods). version 4.0.b10. Sinauer Associates, Sunderland, MA; 2002.
- [65]Guindon S, Gascuel O: A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 2003, 52:696-704.
- [66]Posada D: jModelTest: phylogenetic model averaging. Mol Biol Evol 2008, 25:1253-1256.
- [67]Schwarz G: Estimating dimensions of a model. Ann Stat 1978, 6:461-464.
- [68]Shimodaira H, Hasegawa M: Multiple comparisons of log likelihoods with applications to phylogenetic inference. Mol Biol Evol 1999, 16:1114-1116.
- [69]Felsenstein J: Confidence-limits on phylogenies - an approach using the bootstrap. Evol 1985, 39:783-791.
- [70]Stamatakis A: RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinforma 2006, 22:2688-2690.
- [71]Ronquist F, Huelsenbeck J: MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinforma 2003, 19:1572-1574.
- [72]Rambaut A, Drummond A: Tracer. version 1.4, ; 2007. Available from http://beast.bio.ed.ac.uk/Tracer
- [73]Brandley M, Schmitz A, Reeder T: Partitioned Bayesian analyses, partition choice, and the phylogenetic relationships of scincid lizards. Syst Biol 2005, 54:373-390.
- [74]Kass R, Raftery A: Bayes factors. J Am Stat Assoc 1995, 90:773.
- [75]Lartillot N, Philippe H: Computing Bayes factors using thermodynamic integration. Syst Biol 2006, 55:195-207.
- [76]Fan Y, Wu R, Chen M, Kuo L, Lewis P: Chossing among partition models in Bayesian phylogenetics. Mol Biol Evol 2010, 28:523-532.
- [77]Xie W, Lewis P, Fan Y, Kuo L, Chen M: Improving marginal likelihood estimation for Bayesian phylogenetic model selection. Syst Biol 2011, 60:150-160.
- [78]Drummond A, Rambaut A: BEAST: Bayesian evolutionary analysis by sampling trees. Bmc Evol Biol 2007, 7:214.
PDF