Genetics, Morphology, Advertisement Calls, and Historical Records Distinguish Six New Polyploid Species of African Clawed Frog (Xenopus, Pipidae) from West and Central Africa

. 2015 ; 10 (12) : e0142823. [epub] 20151216

Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid26672747

African clawed frogs, genus Xenopus, are extraordinary among vertebrates in the diversity of their polyploid species and the high number of independent polyploidization events that occurred during their diversification. Here we update current understanding of the evolutionary history of this group and describe six new species from west and central sub-Saharan Africa, including four tetraploids and two dodecaploids. We provide information on molecular variation, morphology, karyotypes, vocalizations, and estimated geographic ranges, which support the distinctiveness of these new species. We resurrect Xenopus calcaratus from synonymy of Xenopus tropicalis and refer populations from Bioko Island and coastal Cameroon (near Mt. Cameroon) to this species. To facilitate comparisons to the new species, we also provide comments on the type specimens, morphology, and distributions of X. epitropicalis, X. tropicalis, and X. fraseri. This includes significantly restricted application of the names X. fraseri and X. epitropicalis, the first of which we argue is known definitively only from type specimens and possibly one other specimen. Inferring the evolutionary histories of these new species allows refinement of species groups within Xenopus and leads to our recognition of two subgenera (Xenopus and Silurana) and three species groups within the subgenus Xenopus (amieti, laevis, and muelleri species groups).

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Tinsley RC, Loumont C, Kobel HR. Geographical distribution and ecology In: Tinsley RC, Kobel HR, editors. The Biology of Xenopus. Oxford: Clarendon Press; 1996. p. 35–59.

Furman BLS, Bewick AJ, Harrison TL, Greenbaum E, GvoŽdík V, Kusamba C, et al. Pan–African phylogeography of a model organism, the African clawed frog "Xenopus laevis" . Mol Ecol. 2015;24(4):909–25. 10.1111/mec.13076 PubMed DOI

Mohneke M, Onadeko AB, Hirschfeld M, Rödel M- O. Dried or fried: Amphibians in local and regional food markets in West Africa. TRAFFIC Bulletin. 2010;22:117–28.

Shapiro HA, Zwarenstein H. A rapid test for pregnancy of Xenopus laevis . Nature. 1934;133:762.

Cannatella DC, de Sá RO. Xenopus laevis as a model organism. Syst Bio. 1993;42(4):476–507.

Harland RM, Grainger RM. Xenopus research: Metamorphosed by genetics and genomics. Trends Genet. 2011;27(12):507–15. 10.1016/j.tig.2011.08.003 PubMed DOI PMC

Hellsten U, Harland RM, Gilchrist MJ, Hendrix D, Jurka J, Kaptonov V, et al. The genome of the western clawed frog Xenopus tropicalis . Science. 2010;328:633–6. 10.1126/science.1183670 PubMed DOI PMC

Bowes JB, Snyder KA, Segerdell E, Gibb R, Jarabek CJ, Pollet N, et al. Xenbase: A Xenopus biology and genomics resource. Nucleic Acids Research. 2009;36:D761–72. PubMed PMC

Bewick AJ, Chain FJJ, Heled J, Evans BJ. The pipid root. Syst Bio. 2012;61(5):913–26. PubMed

Evans BJ. Genome evolution and speciation genetics of allopolyploid clawed frogs (Xenopus and Silurana). Front Biosci. 2008;13:4687–706. PubMed

Cannatella DC, Trueb L. Evolution of pipoid frogs: Intergeneric relationships of the aquatic frog family Pipidae (Anura). Zoological Journal of the Linnean Society. 1988;94:1–38.

Trueb L. Historical constraints and morphological novelties in the evolution of the skeletal system of pipid frogs (Anura: Pipidae) In: Tinsley RC, Kobel HR, editors. The Biology of Xenopus. Oxford: Clarendon Press; 1996. p. 349–77.

Hedke SM, Morgan MJ, Cannatella DC, Hillis DM. Targeted enrichment: Maximizing orthologous gene comparisons across deep evolutionary time. PLOS One. 2013;e67908 10.1371/journal.pone.0067908 PubMed DOI PMC

Irisarri I, Vences M, San Mauro D, Glaw F, Zardoya R. Reversal to air-driven sound production revealed by a molecular phylogeny of tongueless frogs, family Pipidae. BMC Evol Biol. 2011;11:114 10.1186/1471-2148-11-114 PubMed DOI PMC

Kobel HR, Loumont C, Tinsley RC. The extant species In: Tinsley RC, Kobel HR, editors. The Biology of Xenopus. Oxford: Clarendon Press; 1996. p. 9–33.

Evans BJ. Ancestry influences the fate of duplicated genes millions of years after duplication in allopolyploid clawed frogs (Xenopus). Genetics. 2007;176:1119–30. PubMed PMC

Kobel H, Barandun B, Thiebaud CH. Mitochondrial rDNA phylogeny in Xenopus . Herpetological Journal. 1998;8:13–7.

Bewick AJ, Anderson DW, Evans BJ. Evolution of the closely related, sex-related genes DM-W and DMRT1 in African clawed frogs (Xenopus). Evolution. 2011;65(3):698–712. 10.1111/j.1558-5646.2010.01163.x PubMed DOI

Evans BJ, Bliss SM, Mendel SA, Tinsley RC. The Rift Valley is a major barrier to dispersal of African clawed frogs (Xenopus) in Ethiopia. Mol Ecol. 2011;20:4216–30. 10.1111/j.1365-294X.2011.05262.x PubMed DOI

Evans BJ, Carter TF, Hanner R, Tobias ML, Kelley DB, Hanner R, et al. A new species of clawed frog (genus Xenopus), from the Itombwe Plateau, Democratic Republic of the Congo: Implications for DNA barcodes and biodiversity conservation. Zootaxa. 2008;1780:55–68.

Evans BJ, Greenbaum E, Kusamba C, Carter TF, Tobias ML, Mendel SA, et al. Description of a new octoploid frog species (Anura: Pipidae: Xenopus) from the Democratic Republic of the Congo, with a discussion of the biogeography of African clawed frogs in the Albertine Rift. J Zool, Lond. 2011;283:276–90. PubMed PMC

Evans BJ, Kelley DB, Melnick DJ, Cannatella DC. Evolution of RAG-1 in polyploid clawed frogs. Mol Biol Evol. 2005;22(5):1193–207. PubMed

Evans BJ, Kelley DB, Tinsley RC, Melnick DJ, Cannatella DC. A mitochondrial DNA phylogeny of clawed frogs: Phylogeography on sub-Saharan Africa and implications for polyploid evolution. Mol Phylogenet Evol. 2004;33:197–213. PubMed

Evans BJ, Morales JC, Picker MD, Kelley DB, Melnick DJ. Absence of extensive introgression between Xenopus gilli and Xenopus laevis laevis (Anura: Pipidae), in southwestern Cape Province, South Africa. Copeia. 1998;1998(2):504–9.

Kobel HR, Du Pasquier L, Tinsley RC. Natural hybridization and gene introgression between Xenopus gilli and Xenopus laevis laevis (Anura: Pipidae). J Zool, Lond. 1981;194:317–22.

Fischer WJ, Koch WA, Elepfandt A. Sympatry and hybridization between the clawed frogs Xenopus laevis laevis and Xenopus muelleri (Pipidae). J Zool, Lond. 2000;252:99–107.

Picker MD, Harrison JA, Wallace D. Natural hybridization between Xenopus laevis laevis and X. gilli in the southwestern Cape Province, South Africa In: Tinsley RC, Kobel HR, editors. The Biology of Xenopus. Oxford: Clarendon Press; 1996. p. 61–71.

Yager DD. Sound production and acoustic communication in Xenopus borealis In: Tinsley RC, Kobel HR, editors. The Biology of Xenopus. Oxford: Clarendon Press; 1996. p. 121–41.

Tinsley RC. A new species of Xenopus (Anura: Pipidae) from the highlands of Ethiopia. Amphibia-Reptilia. 1995;16:375–88.

Tinsley RC, Kobel HR, Fischberg M. The biology and systematics of a new species of Xenopus (Anura: Pipidae) from the highlands of Central Africa. J Zool, Lond. 1979;188:69–102.

Sabaj Pérez MH. Standard symbolic codes for institutional resource collections in herpetology and ichthyology: An Online Reference. Version 5.0 (22 September 2014). American Society of Ichthyologists and Herpetologists. 2014. Available: http://www.asih.org/.

Ivanova NV, deWaard JR, Hebert PDN. An inexpensive, automation-friendly protocol for recovering high-quality DNA. Molecular Ecology Notes. 2006;6(4):998–1002.

Drummond AJ, Rambaut A. BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol Biol. 2007;7:214 PubMed PMC

Cannatella DC. Xenopus in space and time: Fossils, node calibrations, tip-dating, and paleobiography. Cytogenetic and Genome Research. 2015;145:283–301. 10.1159/000438910 PubMed DOI

Darriba D, Taboada GL, Doallo R, Posada D. jModelTest 2: More models, new heuristics and parallel computing. Nature Methods. 2012;9(8):772. PubMed PMC

Guindon S, Gascuel O. A simple, fast and accurate method to estimate large phylogenies by maximum-likelihood. Syst Bio. 2003;52:696–704. PubMed

Rambaut A, Drummond AJ. Tracer v1.5, Available from http://beast.bio.ed.ac.uk/Tracer. 2007.

Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, et al. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs. Nucleic Acids Res. 1997;25(17):3389–402. PubMed PMC

Pokorná M, Rens W, Rovatsos M, Kratochvíl L. A ZZ/ZW sex chromosome system in the thick-tailed gecko (Underwoodisaurus milii; Squamata: Gekkota: Carphodactylidae), a member of the ancient gecko lineage. Cytogenetic and Genome Research. 2014;142(3):190–6. 10.1159/000358847 PubMed DOI

Tinsley RC. Studies on the ecology and systematics of a new species of clawed toad, the genus Xenopus, from western Uganda. J Zool, Lond. 1973;169:1–27.

Shelton PMJ. The lateral line system at metamorphosis in Xenopus laevis (Daudlin). Journal of Embryology and Experimental Morphology. 1970;24:511–24. PubMed

Tobias ML, Evans BJ, Kelley DB. Evolution of advertisement call in African clawed frogs. Behaviour. 2011;148:519–49. PubMed PMC

Tobias ML, Korsh J, Kelley DB. Evolution of male and female release calls in African clawed frogs. Behaviour. 2014;151(9):1313–34.

Wagler J. Untitled footnote. Isis von Oken. 1827;20:726.

Du Preez LH, Kunene N, Hanner R, Giesy JP, Solomon KR, Hosmer A, et al. Population-specific occurrence of testicular ovarian follicles in Xenopus laevis from South Africa. Aq Tox. 2009;95:10–6. PubMed

Estes R. Relationships of the South African fossil frog Eoxenopoides reuningi (Anura, Pipidae). Annals of the South African Museum. 1977;73(2):49–80.

Boulenger GA. On a collection of batrachians and reptiles made in South Africa by Mr. C. H. B. Grant, and presented to the British Museum by Mr. C. D. Rudd. Proceedings of the Zoological Society of London. 1905;1905:248–55.

Henrici AC, Báez AM. First occurrence of Xenopus (Anura: Pipidae) on the Arabian Penninsula: A new species from the Late Oligocene of the Republic of Yemen. Journal of Paleontology. 2001;75(4):870–82.

Gray JE. Notice of a new genus (Silurana) of frogs from West Africa. Annals and Magazine of Natural History, Series 3. 1864;14:315–6.

Vigny C. Morphologie larvaire de 12 espèces et sous-especes du genre Xenopus . Revue Suisse De Zoologie. 1979;86:877–91.

Tymowska J. Polyploidy and cytogenetic variation in frogs of the genus Xenopus In: Green DS, Sessions SK, editors. Amphibian Cytogenetics and Evolution. San Diego: Academic Press; 1991. p. 259–97.

Tinsley RC. Evolutionary inferences from host and parasite co-speciation In: Tinsley RC, Kobel HR, editors. The Biology of Xenopus. Oxford: Oxford University Press; 1996. p. 403–20.

Jackson JA, Tinsley RC. Evolutionary relationships, host range and geographical distribution of Camallanus Railliet & Henry, 1915 species (Nematoda: Camallaninae) from clawed toads of the genus Xenopus (Anura: Pipidae). Systematic Parasitology. 1995;32:1–21.

Peters WCH. Über die von Hrn. Professor Dr. R. Buchholz in Westafrika gesammelten Amphibien. Monatsberichte der Königlichen Preussische Akademie des Wissenschaften zu Berlin 1875. 1875:196–212.

Fischberg M, Colombelli B, Picard J- J. Diagnose preliminaire d'une espece nouvelle de Xenopus du Zaire. Alytes. 1982;1(4):53–5.

Bauer AM, Günther R, Roebeck HE. An annotated type catalogue of the hemisotid, microhylid, myobatrachid, pelobatid and pipid frogs in the Zoological Museum, Berlin (Amphibia: Anura: Hemisotidae, Microhylidae, Myobatrachidae, Pelobatidae and Pipidae). Mitteilungen aus dem Zoologischen Museum in Berlin. 1996; 72:259–75.

Herrmann H-J. Die Amphibientypen des Zoologischen Museums Greifswald. Veröffentlichungen des Naturhistorischen Museums Schleusingen. 1989;4:13–4.

Müller L. Beiträge zur Herpetologie Kameruns. Abhandlungen der Mathematisch-Physikalischen Classe der Königlich Bayerischen Akademie der Wissenschaften. München Abhandlungen der Mathematisch-Physikalischen Classe der Königlich Bayerischen Akademie der Wissenschaften. 1910;24:544–627.

Bewick AJ, Chain FJJ, Zimmerman LB, Sesay A, Gilchrist M, Owens N, et al. A large pseudoautosomal region on the sex chromosomes of the frog Silurana tropicalis . Genome Biol Evol. 2013;5(6):1087–98. 10.1093/gbe/evt073 PubMed DOI PMC

Schmid M, Steinlein C. Chromosome banding in Amphibia. XXXII. The genus Xenopus (Anura, Pipidae). Cytogenetic and Genome Research. 2015;145:201–17. 10.1159/000433481 PubMed DOI

Jackson K, Blackburn DC. A survey of amphibians and reptiles at degraded sites near Pointe-Noire, Kouilou Province, Republic of Congo. Herpetological Conservation and Biology. 2010;5(3):414–29.

Graf JD, Fischberg M. Albumin evolution of polyploid species of the genus Xenopus . Biochemical Genetics. 1986;24:821–37. PubMed

Flajnik MF, Kasahara M, Shum BP, Salter-Cid L, Taylor E, Du Pasquier L. A novel type of class I gene organization in vertebrates: A large family of non-MHC-linked class I genes is expressed at the RNA level in the amphibian Xenopus . EMBO Journal. 1993;12:4385–96. PubMed PMC

Sato K, Flajnik MF, Du Pasquier L, Katagiri M, Kasahara M. Evolution of the MHC: Isolation of class II -Chain cDNA clones from the amphibian Xenopus laevis . Journal of Immunology. 1993;150:2831–43. PubMed

Shum BP, Avila D, Du Pasquier L, Kasahara M, Flajnik MF. Isolation of a classical MHC class I cDNA from an amphibian: Evidence for only one class I locus in the Xenopus MHC. Journal of Immunology 1993;151:5376–86. PubMed

Herrmann H-J. Amphibien im Aquarium. Ulmer, editor. Stuttgart, Germany1994.

Salamone L. Phylogénie moléculaire et biogéographie de la sous-famille des Xenopodinae avec la description de deux nouvelles espèces. L’Hermine (Bulletin de la Société zoologique de Genève). 2006;147:2.

Salamone L, Montoya-Burgos JI. Historical biogeography of Xenopodinae. Abstracts to the Biology conference, 16–17 February 2006. Muséum d'histoire naturelle–Conservatoire et Jardin botaniques: Université de Genève, Genève; 2006. p. 11–2.

Mechkarska M, Eman A, Coquet L, Leprince J, Jouenne T, Vaudry H, et al. Genome duplications within the Xenopodinae do not increase the multiplicity of antimicrobial peptides in Silurana paratropicalis and Xenopus andrei skin secretions. Comparative Biochemistry and Physiology Part D: Genomics and Proteomics. 2011;6(2):206–12. PubMed

Conlon JM, Mechkarska M, Prajeep M, Sonnevend A, Coquet L, Leprince J, et al. Host-defense peptides in skin secretions of the tetraploid frog Silurana epitropicalis with potent activity against methicillin-resistant Staphylococcus aureus (MRSA). Peptides. 2012;37:113–9. 10.1016/j.peptides.2012.07.005 PubMed DOI

Brown RW. Composition of Scientific Words. Washington D. C., USA: Smithsonian Institution Press; 1956. 882 p.

Blackburn DC, Beier M. "Xenopus paratropicalis" is not a valid name. Zootaxa. 2011;3035:57–8.

Nieuwkoop PD, Faber J. Normal table of Xenopus laevis (Daudin) 2nd ed. Amsterdam: North Holland Publishing Co.; 1967.

Jackson JA, Tinsley RC. Host-specificity and distribution of cephalochlamydid cestodes: Correlation with allopolyploid evolution of pipid hosts. J Zool, Lond. 2001;254:405–19.

Tinsley RC, Jackson JA. Speciation of Protopolystoma Bychowsky, 1957 (Monogenea: Polystomatidae) in hosts of the genus Xenopus (Anura: Pipidae). Systematic Parasitology. 1998;40:93–141.

Tinsley RC, Jackson JA. Correlation of parasite speciation and specificity with host evolutionary relationships. International Journal for Parasitology. 1998;28:1573–82. PubMed

Zimkus BM, Gvoždík V. Sky islands of the Cameroon Volcanic Line: A diversification hot spot for puddle frogs (Phrynobatrachidae: Phrynobatrachus) Zoologica Scripta. 2013;42:591–611.

Günther ACLG. Catalogue of the Batrachia Salientia in the Collection of the British Museum. London: British Museum (Natural History). Department of Zoology; 1858.

Boulenger GA. Catalogue of the Batrachia Salientia s Ecaudata in the collection of the British Museum. London: British Museum of Natural History; 1882. 25 p.

Law R. Ouidah The Social History of a West African Slaving port 1727–1892. Athens: Ohio University Press; 2004.

Fisher CT. Fraser, Louis (b. 1819/20–d. in or after 1883) Oxford Dictionary of National Biography. online edn, Jan 2013 ed: Oxford University Press,; 2004.

Rungger D. Xenopus helveticus, an endangered species? International Journal of Developmental Biology. 2002;46(1):49–63. PubMed

Conlon JM, Mechkarska M, Kolodziejek J, Nowotny N, Coquet L, Leprince J, et al. Host-defense peptides from skin secretions of Fraser's clawed frog Xenopus fraseri (Pipidae): Further insight into the evolutionary history of the Xenopodinae. Comparative Biochemistry and Physiology, Part D Genomics Proteomics. 2014;12:45–52. 10.1016/j.cbd.2014.10.001 PubMed DOI

Mechkarska M, Ahmed E, Coquet L, Leprince J, Jouenne T, Vaudry H, et al. Peptidomic analysis of skin secretions demonstrates that the allopatric populations of Xenopus muelleri (Pipidae) are not conspecific. Peptides. 2011;32:1502–8. 10.1016/j.peptides.2011.05.025 PubMed DOI

Ernst R, Schmitz A, Wagner P, Branquima MF, Hölting M. A window to Central African forest history: Distribution of the Xenopus fraseri subgroup south of the Congo Basin, including a first country record of Xenopus andrei from Angola. Salamandra. 2015;52(1):147–55.

Zimkus BM, Larson JG. Xenopus pygmaeus: Geographic distribution (Gabon). Herpetological Review. 2012;43(1):99.

Wagner P, Wilms TM, Rödder D, Schmitz A. A great leap–the first record of Xenopus pygmaeus (Anura: Pipidae) from south of the Congo Basin. Salamandra. 2013;49(4):206–10.

Greenbaum E, Kusamba C. Geographic Distribution. Xenopus ruwenzoriensis (Ruwenzori Clawed Frog). Herpetological Review. 2010;41:376–7.

Lillo F, Dufresnes C, Faraone FP, Lo Valvo M, Stöck M. Identification and potential origin of invasive clawed frogs Xenopus (Anura: Pipidae) in Sicily based on mitochondrial and nuclear DNA. Italian Journal of Zoology. 2013;80(4):566–73.

AmphibiaWeb. Information on amphibian biology and conservation [web application] Berkeley, California: AmphibiaWeb; 2015. Available: http://amphibiaweb.org. Accessed 26 September 2015.

Haramoto Y, Oshima T, Takahashi S, Asshima M, Ito Y, Kurabayashi A. Complete mitochondrial genome of “Xenopus tropicalis” Asashima line (Anura: Pipidae), a possible undescribed species. Mitochondrial DNA. 2015:in press. PubMed

Conlon JM, Mechkarska M, Coquet L, Leprince J, Jouenne T, Vaudry H, et al. Evidence from peptidomic analysis of skin secretions that allopatric populations of Xenopus gilli (Anura: Pipidae) constitute distinct lineages. Peptides. 2014;63:118–25. 10.1016/j.peptides.2014.11.005 PubMed DOI

Evans BJ, Morales JC, Picker MD, Kelley DB, Melnick DJ. Comparative molecular phylogeography of two Xenopus species, X. gilli and X. laevis, in the southwestern Cape Province, South Africa. Mol Ecol. 1997;6(4):333–43. PubMed

Fogell DJ, Tolley KA, Measey GJ. Mind the gaps: Investigating the cause of the current range disjunction in the Cape Platanna, Xenopus gilli (Anura: Pipidae). PeerJ. 2013;1:e166 10.7717/peerj.166 PubMed DOI PMC

Mable BK, Alexandrou MA, Taylor MI. Genome duplication in amphibians and fish: An extended synthesis. J Zool. 2011;284:151–82.

Evans BJ, Pyron RA, Wiens JJ. Polyploidization and sex chromosome evolution in amphibians In: Soltis PS, Soltis DE, editors. Polyploidy and Genome Evolution: Springer Verlag; 2012. p. 385–410.

Schmid M, Evans BJ, Bogart JP. Polyploidy in Amphibia. Cytogenetic and Genome Research. 2015;145:315–30. 10.1159/000431388 PubMed DOI

Zhang P, Liang D, Mao RL, Hillis DM, Wake DB, Cannatella DC. Efficient sequencing of anuran mtDNAs and a mitogenomic exploration of the phylogeny and evolution of frogs. Mol Biol Evol. 2013;30:1899–915. 10.1093/molbev/mst091 PubMed DOI

Roelants K, Gower DJ, Wilkinson M, Loader SP, Biju SD, Guillaume K, et al. Global patterns of diversification in the history of modern amphibians. Proc Nat Acad Sci. 2007;104(3):887–92. PubMed PMC

de Oliveira FB, Molina EC, Marroig G. Paleogeography of the South Atlantic: A route for primates and rodents into the New World? In: Garber PA, Estrada A, Bicca-Marques JC, Heymann EW, Strier KB, editors. South American Primates Comparative perspectives in the study of behavior, ecology, and conservation. New York: Springer; 2006. p. 55–68.

Tinsley RC. Parasites of Xenopus In: Tinsley RC, Kobel HR, editors. The Biology of Xenopus. Oxford: Oxford University Press; 1996. p. 233–61.

Jackson JA, Tinsley RC. Incompatibility of Protopolystoma xenopodis (Monogenea: Polystomatidae) with an octoploid Xenopus species from southern Rwanda. International Journal for Parasitology. 1998;28(8):1195–9. PubMed

Jackson JA, Pleass RJ, Cable J, Bradley JE, Tinsley RC. Heterogeneous interspecific interactions in a host-parasite system. International Journal for Parasitology. 2006;36(13):1341–9. PubMed

Jackson JA, Tinsley RC. Parasite infectivity to hybridising host species: A link between hybrid resistance and allopolyploid speciation? International Journal for Parasitology. 2003;33(2):137–44. PubMed

Maley J. The African rain forest–main characteristics of changes in vegetation and climate from the Upper Cretaceous to the Quaternary. Proceedings of the Royal Society of Edinburgh. 1996;104B:31–73.

Nichol JE. Geomorphological evidence and Pleistocene refugia in Africa. The Geographical Journal. 1999;165(1):79–89.

Dupont LM, Jahns S, Marret F, Ning S. Vegetation change in equatorial West Africa: Time-slices for the last 150 ka. Palaeogeography, Palaeoclimatology, Palaeoecology. 2000;150:95–122.

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