Chloroplast DNA phylogeography suggests a West African centre of origin for the baobab, Adansonia digitata L. (Bombacoideae, Malvaceae)

The African baobab (Adansonia digitata L.) is an emblematic, culturally important, and physically huge tropical tree species whose natural geographical distribution comprises most of tropical Africa, but also small patches of southern Arabia, and several Atlantic and Indian Ocean islands surrounding...

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Published inMolecular ecology Vol. 18; no. 8; pp. 1707 - 1715
Main Authors POCK TSY, JEAN-MICHEL LEONG, LUMARET, ROSELYNE, MAYNE, DIANA, VALL, ABDALLAHI OULD MOHAMED, ABUTABA, YAHIA I. M., SAGNA, MAURICE, RAOSETA, SOAHARIN'NY ONY RAKOTONDRALAMBO, DANTHU, PASCAL
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.04.2009
Wiley
Subjects
Online AccessGet full text
ISSN0962-1083
1365-294X
1365-294X
DOI10.1111/j.1365-294X.2009.04144.x

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Abstract The African baobab (Adansonia digitata L.) is an emblematic, culturally important, and physically huge tropical tree species whose natural geographical distribution comprises most of tropical Africa, but also small patches of southern Arabia, and several Atlantic and Indian Ocean islands surrounding the African continent, notably including Madagascar. We analysed the polymerase chain reaction–restriction fragment length polymorphism of five chloroplast DNA fragments obtained from 344 individuals of A. digitata collected from 74 populations covering the entire extant distribution range of the species. Our goal was to reconstruct the phylogeographical history of the species and, if possible, to identify its centre of origin, which has been a subject of controversy for many decades. We identified five haplotypes whose distribution is clearly geographically structured. Using several species of Adansonia and of closely related genera as outgroups, the haplotypes showed a clear phylogeographical pattern of three groups. Two are phylogenetically related to the outgroup taxa, and are distributed in West Africa. The third group is substantially more differentiated genetically from outgroup species, and it corresponds to southern and eastern Africa, Arabia and the Indian Ocean islands, including Madagascar. According to our results, the tetraploid A. digitata, or its diploid progenitor, probably originated in West Africa and migrated subsequently throughout the tropical parts of that continent, and beyond, by natural and human‐mediated terrestrial and overseas dispersal.
AbstractList The African baobab (Adansonia digitata L.) is an emblematic, culturally important, and physically huge tropical tree species whose natural geographical distribution comprises most of tropical Africa, but also small patches of southern Arabia, and several Atlantic and Indian Ocean islands surrounding the African continent, notably including Madagascar. We analysed the polymerase chain reaction-restriction fragment length polymorphism of five chloroplast DNA fragments obtained from 344 individuals of A. digitata collected from 74 populations covering the entire extant distribution range of the species. Our goal was to reconstruct the phylogeographical history of the species and, if possible, to identify its centre of origin, which has been a subject of controversy for many decades. We identified five haplotypes whose distribution is clearly geographically structured. Using several species of Adansonia and of closely related genera as outgroups, the haplotypes showed a clear phylogeographical pattern of three groups. Two are phylogenetically related to the outgroup taxa, and are distributed in West Africa. The third group is substantially more differentiated genetically from outgroup species, and it corresponds to southern and eastern Africa, Arabia and the Indian Ocean islands, including Madagascar. According to our results, the tetraploid A. digitata, or its diploid progenitor, probably originated in West Africa and migrated subsequently throughout the tropical parts of that continent, and beyond, by natural and human-mediated terrestrial and overseas dispersal.
The African baobab (Adansonia digitata L.) is an emblematic, culturally important, and physically huge tropical tree species whose natural geographical distribution comprises most of tropical Africa, but also small patches of southern Arabia, and several Atlantic and Indian Ocean islands surrounding the African continent, notably including Madagascar. We analysed the polymerase chain reaction-restriction fragment length polymorphism of five chloroplast DNA fragments obtained from 344 individuals of A. digitata collected from 74 populations covering the entire extant distribution range of the species. Our goal was to reconstruct the phylogeographical history of the species and, if possible, to identify its centre of origin, which has been a subject of controversy for many decades. We identified five haplotypes whose distribution is clearly geographically structured. Using several species of Adansonia and of closely related genera as outgroups, the haplotypes showed a clear phylogeographical pattern of three groups. Two are phylogenetically related to the outgroup taxa, and are distributed in West Africa. The third group is substantially more differentiated genetically from outgroup species, and it corresponds to southern and eastern Africa, Arabia and the Indian Ocean islands, including Madagascar. According to our results, the tetraploid A. digitata, or its diploid progenitor, probably originated in West Africa and migrated subsequently throughout the tropical parts of that continent, and beyond, by natural and human-mediated terrestrial and overseas dispersal. [PUBLICATION ABSTRACT]
The African baobab (Adansonia digitata L.) is an emblematic, culturally important, and physically huge tropical tree species whose natural geographical distribution comprises most of tropical Africa, but also small patches of southern Arabia, and several Atlantic and Indian Ocean islands surrounding the African continent, notably including Madagascar. We analysed the polymerase chain reaction-restriction fragment length polymorphism of five chloroplast DNA fragments obtained from 344 individuals of A. digitata collected from 74 populations covering the entire extant distribution range of the species. Our goal was to reconstruct the phylogeographical history of the species and, if possible, to identify its centre of origin, which has been a subject of controversy for many decades. We identified five haplotypes whose distribution is clearly geographically structured. Using several species of Adansonia and of closely related genera as outgroups, the haplotypes showed a clear phylogeographical pattern of three groups. Two are phylogenetically related to the outgroup taxa, and are distributed in West Africa. The third group is substantially more differentiated genetically from outgroup species, and it corresponds to southern and eastern Africa, Arabia and the Indian Ocean islands, including Madagascar. According to our results, the tetraploid A. digitata, or its diploid progenitor, probably originated in West Africa and migrated subsequently throughout the tropical parts of that continent, and beyond, by natural and human-mediated terrestrial and overseas dispersal.The African baobab (Adansonia digitata L.) is an emblematic, culturally important, and physically huge tropical tree species whose natural geographical distribution comprises most of tropical Africa, but also small patches of southern Arabia, and several Atlantic and Indian Ocean islands surrounding the African continent, notably including Madagascar. We analysed the polymerase chain reaction-restriction fragment length polymorphism of five chloroplast DNA fragments obtained from 344 individuals of A. digitata collected from 74 populations covering the entire extant distribution range of the species. Our goal was to reconstruct the phylogeographical history of the species and, if possible, to identify its centre of origin, which has been a subject of controversy for many decades. We identified five haplotypes whose distribution is clearly geographically structured. Using several species of Adansonia and of closely related genera as outgroups, the haplotypes showed a clear phylogeographical pattern of three groups. Two are phylogenetically related to the outgroup taxa, and are distributed in West Africa. The third group is substantially more differentiated genetically from outgroup species, and it corresponds to southern and eastern Africa, Arabia and the Indian Ocean islands, including Madagascar. According to our results, the tetraploid A. digitata, or its diploid progenitor, probably originated in West Africa and migrated subsequently throughout the tropical parts of that continent, and beyond, by natural and human-mediated terrestrial and overseas dispersal.
The African baobab ( Adansonia digitata L.) is an emblematic, culturally important, and physically huge tropical tree species whose natural geographical distribution comprises most of tropical Africa, but also small patches of southern Arabia, and several Atlantic and Indian Ocean islands surrounding the African continent, notably including Madagascar. We analysed the polymerase chain reaction–restriction fragment length polymorphism of five chloroplast DNA fragments obtained from 344 individuals of A. digitata collected from 74 populations covering the entire extant distribution range of the species. Our goal was to reconstruct the phylogeographical history of the species and, if possible, to identify its centre of origin, which has been a subject of controversy for many decades. We identified five haplotypes whose distribution is clearly geographically structured. Using several species of Adansonia and of closely related genera as outgroups, the haplotypes showed a clear phylogeographical pattern of three groups. Two are phylogenetically related to the outgroup taxa, and are distributed in West Africa. The third group is substantially more differentiated genetically from outgroup species, and it corresponds to southern and eastern Africa, Arabia and the Indian Ocean islands, including Madagascar. According to our results, the tetraploid A. digitata , or its diploid progenitor, probably originated in West Africa and migrated subsequently throughout the tropical parts of that continent, and beyond, by natural and human‐mediated terrestrial and overseas dispersal.
Author RAOSETA, SOAHARIN'NY ONY RAKOTONDRALAMBO
DANTHU, PASCAL
POCK TSY, JEAN-MICHEL LEONG
LUMARET, ROSELYNE
SAGNA, MAURICE
VALL, ABDALLAHI OULD MOHAMED
ABUTABA, YAHIA I. M.
MAYNE, DIANA
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Issue 8
Keywords cpDNA PCR-RFLP variation
Bombacoideae
African baobab
Adansonia digitata L
phylogeography
Language English
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PublicationDecade 2000
PublicationPlace Oxford, UK
PublicationPlace_xml – name: Oxford, UK
– name: England
– name: Oxford
PublicationTitle Molecular ecology
PublicationTitleAlternate Mol Ecol
PublicationYear 2009
Publisher Blackwell Publishing Ltd
Wiley
Publisher_xml – name: Blackwell Publishing Ltd
– name: Wiley
References Baum DA, Oginuma K (1994) A review of some chromosome numbers in Bombacaceae with new counts for Adansonia (Bombacaceae). Taxon, 43, 11-20.
Grivet D, Heinse B, Vendramin GG, Petit RJ (2001) Genome walking with consensus primers: application to the large single copy region of chloroplast DNA. Molecular Ecology Notes, 1, 345-349.
Swofford D (2000) paup*: Phylogenetic Analysis Using Parsimony (and Other Methods). Beta version 4.0b10. Sinauer & Associates, Sunderland, Massachusetts.
Magri D, Fineschi S, Bellarosa R et al . (2007) The distribution of Quercus suber chloroplast haplotypes matches the palaeogeographical history of the western Mediterranean. Molecular Ecology, 16, 5259-5266.
Baum DA, Smith SD, Yen A et al . (2004) Phylogenetic relationships of Malvatheca (Bombacoideae and Malvoideae; Malvaceae sensu lato) as inferred from plastid DNA sequences. American Journal of Botany, 91, 1863-1871.
Baum DA, Small RL, Wendel JF (1998) Biogeography and floral evolution of Baobabs (Adansonia, Bombacaceae), as inferred from multiple data sets. Systematic Biology, 47, 181-207.
Armstrong PH (1983) The disjunct distribution of the genus Adansonia L. National Geographic Journal of India, 29, 142-163.
Wickens GE, Lowe P (2008) The Baobabs, Pachycauls of Africa, Madagascar and Australia. Springer, Berlin, Heidelberg, New York.
Baum DA (1995) A systematic revision of Adansonia (Bombacaceae). Annals of Missouri Botanical Garden, 82, 440-470.
Leigh EG, Hladik A, Hladik CM, Jolly A (2007) The biogeography of large islands, or how does the size of the ecological theater affect the evolutionary play? Revue Ecologique (Terre Vie), 62, 105-168.
Pãtrut A, Von Reden KF, Lowry DA et al . (2007) Radiocarbon dating of a very large African baobab. Tree Physiology, 27, 1569-1574.
Danthu P, Roussel J, Gaye A, El Mazzoudi EH (1995) Baobab (Adansonia digitata L.) seed pretreatments for germination improvement. Seed Science and Technology, 23, 469-475.
Kubitzki K, Bayer C (2002) Flowering Plants-Dicotyledons: Malvales, Capparales and Non-Betalain Caryophyllales. Springer, Berlin, Heidelberg, New York.
Lumaret R, Tryphon-Dionnet M, Michaud H et al . (2005) Phylogeographycal variation of chloroplast DNA in Cork oak (Quercus suber L.). Annals of Botany, 96, 853-861.
Pons O, Petit RJ (1996) Measuring and testing genetic differentiation with ordered versus unordered alleles. Genetics, 144, 1237-1245.
Bingham MG (1994) Did the Baobabs originate in Madagascar? Ingens Bulletin, 10, 12.
Magni CR, Ducousso A, Caron H, Petit RJ, Kremer A (2005) Chloroplast DNA variation of Quercus rubra L. in North America and comparison with other Fagaceae. Molecular Ecology, 14, 513-524.
Ravi V, Khurana JP, Tyagi AK, Khurana P (2008) An update on chloroplast genomes. Plant Systematics and Evolution, 271, 101-122.
Aubréville A (1975) Essais de géophylétique de Bombacacées. Adansonia Sér, 2 (15), 57-64.
Weeks A, Daly DC, Simpson BB (2005) The phylogenetic history and biogeography of the frankincense and myrrh family (Burseraceae) based on nuclear and chloroplast sequence data. Molecular Phylogenetics and Evolution, 35, 85-101.
Lumaret R (1988) Adaptive strategies and ploidy levels. Acta Oecologica, Oecologia Plantarum, 9, 83-93.
Monod T (1960) Notes botaniques sur les îles de São Tomé et de Principe. Bulletin de l'Institut Fondamental d'Afrique Noire, 22, 19-83.
Wickens GE (1982) The baobab-Africa's upside-down tree. Kew Bulletin, 37, 173-209.
Pons O, Petit RJ (1995) estimation, variance and optimal sampling of gene diversity. I. Haploid locus. Theoretical and Applied Genetics, 90, 462-470.
Chevalier A (1906) Les baobabs (Adansonia) de l'Afrique continentale. Bulletin de la Société Botanique de France, 53, 480-496.
Gao LM, Möller M, Zhang XM et al . (2007) High variation and strong phylogeographic pattern among cpDNA haplotypes in Taxus wallichiana (Taxaceae) in China and North Vietnam. Molecular Ecology, 16, 4684-4696.
Meve U, Liede S (2002) Floristic exchange between mainland Africa and Madagascar: case studies in Apocynaceae-Asclepiadoideae. Journal of Biogeography, 29, 865-873.
Jimenez P, Lopez de Heredia U, Collada C, Lorenzo Z, Gil L (2004) High variability of chloroplast DNA in three Mediterranean evergreen oaks indicates complex evolutionary history. Heredity, 93, 510-515.
Swart ER (1963) Age of the baobab tree. Nature, 198, 708-709.
Alverson WS, Whitlock B, Nyfeller R, Bayer C, Baum DA (1999) Phylogeny of the core Malvales from NDHL sequence data. American Journal of Botany, 86, 1474-1486.
Dumolin-Lapègue S, Pemonge MH, Petit RJ (1997) An enlarged set of consensus primers for the study of organelle DNA in plants. Molecular Ecology, 6, 393-397.
Demesure B, Sodzi N, Petit RJ (1995) A set of universal primers for amplification of polymorphic non-coding regions of mitochondrial and chloroplast DNA in plants. Molecular Ecology, 4, 129-131.
Vendramin GG, Fady B, González-Martinez C et al . (2008) Genetically depauperate but widespread: the case of an emblematic Mediterranean pine. Evolution, 62, 680-688.
Dick CW, Abdul-Salim K, Bermingham Dick E (2003) Molecular systematic analysis reveals cryptic tertiary diversification of a widespread tropical rain forest tree. American Naturalist, 162, 691-703.
Wickens GE (1979) Speculations on seed dispersal and the flora of the Aldabra archipelago. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 286, 85-97.
De Queiroz A (2004) The resurrection of oceanic dispersal in historical biogeography. Trends in Ecology & Evolution, 20, 68-73.
Soltis DE, Soltis PS, Tate JA (2003) Advances in the study of polyploidy since Plant speciation. New Phytologist, 161, 173-191.
Bandelt HJ, Forster P, Röhl A (1999) Median-joining networks for inferring intraspecific phylogenies. Molecular Biology and Evolution, 16, 37-48.
Dick CW, Bermingham E, Lemes MR, Gribel R (2007) Extreme long-distance dispersal of the lowland tropical rainforest tree Ceiba pentandra L. (Malvaceae) in Africa and the Neotropics. Molecular Ecology, 16, 3039-3049.
2004; 20
1982; 37
1963; 198
1979; 286
1995; 90
1906; 53
2008
1999; 86
1996; 144
2003
2002
2004; 91
1997; 6
1995; 4
1979
1994; 43
1998; 47
2007; 16
1995; 82
1960; 22
2002; 29
2004; 93
1988; 9
2000
1999; 16
1995; 23
2003; 162
2005; 96
2003; 161
1975; 2
2001; 1
2007; 62
1983; 29
2008; 62
1994; 10
2008; 271
2005; 35
2005; 14
2007; 27
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Leigh EG (e_1_2_6_23_1) 2007; 62
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Armstrong PH (e_1_2_6_4_1) 1983; 29
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Armstrong PH (e_1_2_6_3_1) 1979
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Aubréville A (e_1_2_6_5_1) 1975; 2
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Bingham MG (e_1_2_6_12_1) 1994; 10
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Kubitzki K (e_1_2_6_22_1) 2002
De Queiroz A (e_1_2_6_33_1) 2004; 20
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Lumaret R (e_1_2_6_24_1) 1988; 9
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References_xml – reference: Wickens GE, Lowe P (2008) The Baobabs, Pachycauls of Africa, Madagascar and Australia. Springer, Berlin, Heidelberg, New York.
– reference: Gao LM, Möller M, Zhang XM et al . (2007) High variation and strong phylogeographic pattern among cpDNA haplotypes in Taxus wallichiana (Taxaceae) in China and North Vietnam. Molecular Ecology, 16, 4684-4696.
– reference: Pons O, Petit RJ (1996) Measuring and testing genetic differentiation with ordered versus unordered alleles. Genetics, 144, 1237-1245.
– reference: Monod T (1960) Notes botaniques sur les îles de São Tomé et de Principe. Bulletin de l'Institut Fondamental d'Afrique Noire, 22, 19-83.
– reference: Chevalier A (1906) Les baobabs (Adansonia) de l'Afrique continentale. Bulletin de la Société Botanique de France, 53, 480-496.
– reference: Bingham MG (1994) Did the Baobabs originate in Madagascar? Ingens Bulletin, 10, 12.
– reference: Meve U, Liede S (2002) Floristic exchange between mainland Africa and Madagascar: case studies in Apocynaceae-Asclepiadoideae. Journal of Biogeography, 29, 865-873.
– reference: Dumolin-Lapègue S, Pemonge MH, Petit RJ (1997) An enlarged set of consensus primers for the study of organelle DNA in plants. Molecular Ecology, 6, 393-397.
– reference: De Queiroz A (2004) The resurrection of oceanic dispersal in historical biogeography. Trends in Ecology & Evolution, 20, 68-73.
– reference: Swart ER (1963) Age of the baobab tree. Nature, 198, 708-709.
– reference: Magri D, Fineschi S, Bellarosa R et al . (2007) The distribution of Quercus suber chloroplast haplotypes matches the palaeogeographical history of the western Mediterranean. Molecular Ecology, 16, 5259-5266.
– reference: Baum DA, Oginuma K (1994) A review of some chromosome numbers in Bombacaceae with new counts for Adansonia (Bombacaceae). Taxon, 43, 11-20.
– reference: Baum DA (1995) A systematic revision of Adansonia (Bombacaceae). Annals of Missouri Botanical Garden, 82, 440-470.
– reference: Dick CW, Bermingham E, Lemes MR, Gribel R (2007) Extreme long-distance dispersal of the lowland tropical rainforest tree Ceiba pentandra L. (Malvaceae) in Africa and the Neotropics. Molecular Ecology, 16, 3039-3049.
– reference: Lumaret R, Tryphon-Dionnet M, Michaud H et al . (2005) Phylogeographycal variation of chloroplast DNA in Cork oak (Quercus suber L.). Annals of Botany, 96, 853-861.
– reference: Vendramin GG, Fady B, González-Martinez C et al . (2008) Genetically depauperate but widespread: the case of an emblematic Mediterranean pine. Evolution, 62, 680-688.
– reference: Lumaret R (1988) Adaptive strategies and ploidy levels. Acta Oecologica, Oecologia Plantarum, 9, 83-93.
– reference: Baum DA, Small RL, Wendel JF (1998) Biogeography and floral evolution of Baobabs (Adansonia, Bombacaceae), as inferred from multiple data sets. Systematic Biology, 47, 181-207.
– reference: Armstrong PH (1983) The disjunct distribution of the genus Adansonia L. National Geographic Journal of India, 29, 142-163.
– reference: Kubitzki K, Bayer C (2002) Flowering Plants-Dicotyledons: Malvales, Capparales and Non-Betalain Caryophyllales. Springer, Berlin, Heidelberg, New York.
– reference: Pons O, Petit RJ (1995) estimation, variance and optimal sampling of gene diversity. I. Haploid locus. Theoretical and Applied Genetics, 90, 462-470.
– reference: Ravi V, Khurana JP, Tyagi AK, Khurana P (2008) An update on chloroplast genomes. Plant Systematics and Evolution, 271, 101-122.
– reference: Magni CR, Ducousso A, Caron H, Petit RJ, Kremer A (2005) Chloroplast DNA variation of Quercus rubra L. in North America and comparison with other Fagaceae. Molecular Ecology, 14, 513-524.
– reference: Pãtrut A, Von Reden KF, Lowry DA et al . (2007) Radiocarbon dating of a very large African baobab. Tree Physiology, 27, 1569-1574.
– reference: Demesure B, Sodzi N, Petit RJ (1995) A set of universal primers for amplification of polymorphic non-coding regions of mitochondrial and chloroplast DNA in plants. Molecular Ecology, 4, 129-131.
– reference: Jimenez P, Lopez de Heredia U, Collada C, Lorenzo Z, Gil L (2004) High variability of chloroplast DNA in three Mediterranean evergreen oaks indicates complex evolutionary history. Heredity, 93, 510-515.
– reference: Danthu P, Roussel J, Gaye A, El Mazzoudi EH (1995) Baobab (Adansonia digitata L.) seed pretreatments for germination improvement. Seed Science and Technology, 23, 469-475.
– reference: Grivet D, Heinse B, Vendramin GG, Petit RJ (2001) Genome walking with consensus primers: application to the large single copy region of chloroplast DNA. Molecular Ecology Notes, 1, 345-349.
– reference: Weeks A, Daly DC, Simpson BB (2005) The phylogenetic history and biogeography of the frankincense and myrrh family (Burseraceae) based on nuclear and chloroplast sequence data. Molecular Phylogenetics and Evolution, 35, 85-101.
– reference: Dick CW, Abdul-Salim K, Bermingham Dick E (2003) Molecular systematic analysis reveals cryptic tertiary diversification of a widespread tropical rain forest tree. American Naturalist, 162, 691-703.
– reference: Aubréville A (1975) Essais de géophylétique de Bombacacées. Adansonia Sér, 2 (15), 57-64.
– reference: Wickens GE (1979) Speculations on seed dispersal and the flora of the Aldabra archipelago. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 286, 85-97.
– reference: Baum DA, Smith SD, Yen A et al . (2004) Phylogenetic relationships of Malvatheca (Bombacoideae and Malvoideae; Malvaceae sensu lato) as inferred from plastid DNA sequences. American Journal of Botany, 91, 1863-1871.
– reference: Leigh EG, Hladik A, Hladik CM, Jolly A (2007) The biogeography of large islands, or how does the size of the ecological theater affect the evolutionary play? Revue Ecologique (Terre Vie), 62, 105-168.
– reference: Swofford D (2000) paup*: Phylogenetic Analysis Using Parsimony (and Other Methods). Beta version 4.0b10. Sinauer & Associates, Sunderland, Massachusetts.
– reference: Wickens GE (1982) The baobab-Africa's upside-down tree. Kew Bulletin, 37, 173-209.
– reference: Alverson WS, Whitlock B, Nyfeller R, Bayer C, Baum DA (1999) Phylogeny of the core Malvales from NDHL sequence data. American Journal of Botany, 86, 1474-1486.
– reference: Soltis DE, Soltis PS, Tate JA (2003) Advances in the study of polyploidy since Plant speciation. New Phytologist, 161, 173-191.
– reference: Bandelt HJ, Forster P, Röhl A (1999) Median-joining networks for inferring intraspecific phylogenies. Molecular Biology and Evolution, 16, 37-48.
– volume: 23
  start-page: 469
  year: 1995
  end-page: 475
  article-title: Baobab ( L.) seed pretreatments for germination improvement
  publication-title: Seed Science and Technology
– volume: 10
  start-page: 12
  year: 1994
  article-title: Did the Baobabs originate in Madagascar?
  publication-title: Ingens Bulletin
– volume: 82
  start-page: 440
  year: 1995
  end-page: 470
  article-title: A systematic revision of (Bombacaceae)
  publication-title: Annals of Missouri Botanical Garden
– volume: 22
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  year: 1960
  end-page: 83
  article-title: Notes botaniques sur les îles de São Tomé et de Principe
  publication-title: Bulletin de l’Institut Fondamental d’Afrique Noire
– volume: 53
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  year: 1999
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  article-title: Median‐joining networks for inferring intraspecific phylogenies
  publication-title: Molecular Biology and Evolution
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  year: 2003
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– volume: 144
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  article-title: Measuring and testing genetic differentiation with ordered versus unordered alleles
  publication-title: Genetics
– volume: 29
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  year: 1983
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  article-title: The disjunct distribution of the genus L
  publication-title: National Geographic Journal of India
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  article-title: Age of the baobab tree
  publication-title: Nature
– volume: 20
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  year: 2004
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  article-title: The resurrection of oceanic dispersal in historical biogeography
  publication-title: Trends in Ecology & Evolution
– year: 2000
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  start-page: 5259
  year: 2007
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  article-title: The distribution of chloroplast haplotypes matches the palaeogeographical history of the western Mediterranean
  publication-title: Molecular Ecology
– volume: 27
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  year: 2007
  end-page: 1574
  article-title: Radiocarbon dating of a very large African baobab
  publication-title: Tree Physiology
– volume: 62
  start-page: 680
  year: 2008
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  article-title: Genetically depauperate but widespread: the case of an emblematic Mediterranean pine
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  year: 1995
  end-page: 131
  article-title: A set of universal primers for amplification of polymorphic non‐coding regions of mitochondrial and chloroplast DNA in plants
  publication-title: Molecular Ecology
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  article-title: The baobab‐Africa's upside‐down tree
  publication-title: Kew Bulletin
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  year: 2005
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  article-title: Phylogeographycal variation of chloroplast DNA in Cork oak ( L.)
  publication-title: Annals of Botany
– volume: 16
  start-page: 3039
  year: 2007
  end-page: 3049
  article-title: Extreme long‐distance dispersal of the lowland tropical rainforest tree L. (Malvaceae) in Africa and the Neotropics
  publication-title: Molecular Ecology
– volume: 271
  start-page: 101
  year: 2008
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  article-title: An update on chloroplast genomes
  publication-title: Plant Systematics and Evolution
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  year: 2002
  end-page: 873
  article-title: Floristic exchange between mainland Africa and Madagascar: case studies in Apocynaceae‐Asclepiadoideae
  publication-title: Journal of Biogeography
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  year: 1988
  end-page: 93
  article-title: Adaptive strategies and ploidy levels.
  publication-title: Acta Oecologica
– volume: 90
  start-page: 462
  year: 1995
  end-page: 470
  article-title: estimation, variance and optimal sampling of gene diversity. I. Haploid locus
  publication-title: Theoretical and Applied Genetics
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  publication-title: Adansonia Sér
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  article-title: High variation and strong phylogeographic pattern among cpDNA haplotypes in (Taxaceae) in China and North Vietnam
  publication-title: Molecular Ecology
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  year: 2005
  end-page: 524
  article-title: Chloroplast DNA variation of L. in North America and comparison with other Fagaceae
  publication-title: Molecular Ecology
– volume: 1
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  year: 2001
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  article-title: Genome walking with consensus primers: application to the large single copy region of chloroplast DNA
  publication-title: Molecular Ecology Notes
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  article-title: An enlarged set of consensus primers for the study of organelle DNA in plants
  publication-title: Molecular Ecology
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  year: 2004
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  article-title: High variability of chloroplast DNA in three Mediterranean evergreen oaks indicates complex evolutionary history
  publication-title: Heredity
– volume: 35
  start-page: 85
  year: 2005
  end-page: 101
  article-title: The phylogenetic history and biogeography of the frankincense and myrrh family (Burseraceae) based on nuclear and chloroplast sequence data
  publication-title: Molecular Phylogenetics and Evolution
– volume: 91
  start-page: 1863
  year: 2004
  end-page: 1871
  article-title: Phylogenetic relationships of Malvatheca (Bombacoideae and Malvoideae; Malvaceae ) as inferred from plastid DNA sequences
  publication-title: American Journal of Botany
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  year: 2007
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  article-title: The biogeography of large islands, or how does the size of the ecological theater affect the evolutionary play?
  publication-title: Revue Ecologique (Terre Vie)
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  year: 1979
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  article-title: Speculations on seed dispersal and the flora of the Aldabra archipelago
  publication-title: Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
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  article-title: Molecular systematic analysis reveals cryptic tertiary diversification of a widespread tropical rain forest tree
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Snippet The African baobab (Adansonia digitata L.) is an emblematic, culturally important, and physically huge tropical tree species whose natural geographical...
The African baobab ( Adansonia digitata L.) is an emblematic, culturally important, and physically huge tropical tree species whose natural geographical...
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SubjectTerms Adansonia
Adansonia - genetics
Adansonia digitata
Adansonia digitata L
Africa, Western
African baobab
Atlantic Ocean Islands
Biodiversity and Ecology
Biogeography
Bombacoideae
Botany
center of origin
chloroplast DNA
Chloroplasts
cpDNA PCR-RFLP variation
Deoxyribonucleic acid
DNA
DNA, Chloroplast - genetics
Ecology
Environmental Sciences
Evolution, Molecular
Genetics, Population
Geographical distribution
Geography
Germination
Haplotypes
Islands
Madagascar
Malvaceae
Molecular biology
Phylogeny
phylogeography
Plant species
Polymorphism, Restriction Fragment Length
Seawater
Seeds - growth & development
Sequence Analysis, DNA
Taxa
trees
Western Africa
Title Chloroplast DNA phylogeography suggests a West African centre of origin for the baobab, Adansonia digitata L. (Bombacoideae, Malvaceae)
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https://hal.science/cirad-00964068
Volume 18
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