Hybridisation, introgression and climate change: A case study of the tree genus Fraxinus (oleaceae)

Climate Change, Ecology and Systematics

Volumn , Issue , 2011, Pages 320-342

  Thomasset, M ^a   Fernandez Manjarres J F ^b,c   Douglas, G C ^d   Frascaria Lacoste, N ^b,c   Hodkinson, T R ^a  

^a TRINITY COLLEGE DUBLIN   (Ireland)

^b UNIVERSITÉ PARIS SACLAY   (France)

^c AGROPARISTECH   (France)

^d Teagasc   (Ireland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84932156595     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1017/CBO9780511974540.016     Document Type: Chapter

References (114)

1. Alcamo, J., Floerke, M. and Maerker, M. (2007). Future long-term changes in global water resources driven by socio-economic and climatic changes. Hydrological Sciences, 52, 247–275.
2. Allendorf, F. W., Leary, R. F., Spruell, P. and Wenburg, J. K. (2001). The problems with hybrids: setting conservation guidelines. Trends in Ecology and Evolution, 16, 613–622.
3. Anderson, E. and Hubricht, L. (1938). Hybridization in Tradescantia. III. The evidence for introgressive hybridization. American Journal of Botany, 25, 396–402.
4. Anderson, E. and Stebbins, J. (1954). Hybridization as an evolutionary stimulus. Evolution, 8, 378–388.
5. Arnold, M. L. (1997). Natural Hybridization and Evolution. Oxford: Oxford University Press.
6. Arnold, M. L. (2004). Natural hybridization and the evolution of domesticated, pest and disease organisms. Molecular Ecology, 13, 997–1007.
7. Avise, J. C. (2004). Molecular Markers, Natural History, and Evolution, 2nd edn. Sunderland, MA: Sinauer Associates.
8. Broeck, A. V., Cox, K., Quataert, P., van Bockstaele, E. and van Slycken, J. (2003). Flowering phenology of Populus nigra L., P. nigra cv. italica and P. × canadensis Moench. and the potential for natural hybridisation in Belgium. Silvae Genetica, 52, 280–283.
9. Buggs, R. J. A. (2007). Empirical study of hybrid zone movement. Heredity, 99, 301–312.
10. Carroll, C. P. and Borrill, M. (1965). Tetraploid hybrids from crosses between diploid and tetraploid Dactylis and their significance. Genetica, 36, 65–82.
11. Chapman, M. A. and Burke, J. M. (2006). Letting the gene out of the bottle: the population genetics of genetically modified crops. New Phytologist, 170, 429–443.
12. Conceição, A. de S., de Queiroz, L. and Borba, E. (2008). Natural hybrids in Chamaecrista sect. Absus subsect. Baseophyllum (Leguminosae– Caesalpinioideae): genetic and morphological evidence. Plant Systematics and Evolution, 271, 19–27.
13. Cottignies, A. (1986). The hydrolysis of starch as related to the interruption of dormancy in the ash bud. Journal of Plant Physiology, 123, 373–380.
14. Coyer, J. A., Hoarau, G., Stam, W. T. and Olsen, J. L. (2007). Hybridization and introgression in a mixed population of the intertidal seaweeds Fucus evanescens and F. serratus. Journal of Evolutionary Biology, 20, 2322–2333.
15. Coyne, J. A. and Orr, H. A. (2004). Speciation. Sunderland, MA: Sinauer Associates.
16. Currat, M., Ruedi, M., Petit, R. J. and Excoffier, L. (2008). The hidden side of invasions: massive introgression by local genes. Evolution, 62, 1908–1920.
17. Curtu, A. L., Gailing, O. and Finkeldey, R. (2007). Evidence for hybridization and introgression within a speciesrich oak (Quercus spp.) community. BioMed Central Evolutionary Biology, 7, 218–233.
18. Dobzhansky, T. (1937). Genetics and the Origin of Species. New York, NY: Cambridge University Press.
19. Donnelly, A, Salamin, N. and Jones, M. B. (2006). Changes in tree phenology: an indicator of spring warming in Ireland? Biology and Environment, Proceedings of the Royal Irish Academy, 106B, 49–56.
20. Duffy, P. B., Govindasamy, B., Lorio, J. P. et al. (2003). High-resolution simulations of global climate, part 1: present climate. Climate Dynamics, 21, 371–390.
21. Ebina, T. and Otho, K. (2006). Morphological characters and PCRRFLP markers in the interspecific hybrids between Bactrocera carambolae and B. papayae of the B. dorsalis species complex (Diptera: Tephritidae). Research Bulletin of the Plant Protection Service, Japan, 42, 23–34.
22. Ellstrand, N. C. and Schierenbeck, K. A. (2000). Hybridization as a stimulus for the evolution of invasiveness in plants? Euphytica, 148, 35–46.
23. Ellstrand, N. C., Prentice, H. C. and Hancock, J. F. (1999). Gene flow and introgression from domesticated plants into their wild relatives. Annual Review of Ecology and Systematics, 30, 539–563.
24. Fernández-Manjarrés, J. F., Gerard, P. R., Dufour, J., Raquin, C. and Frascaria of morphological and molecular hybridization between Fraxinus excelsior L. and Fraxinus angustifolia Vahl (Oleaceae) in eastern and western France. Molecular Ecology, 15, 3245–3257.
25. Fielding, A. H. and Bell, J. F. (1997). A review of methods for the assessment of prediction errors in conservation presence/absence models. Environmental Conservation, 24, 38–49.
26. Fitter, A. H. and Fitter, R. S. R. (2002). Rapid changes in flowering time in British plants. Science, 296, 1689–1691.
27. Foden, W., Midgley, G. F., Hughes, G. O. et al. (2007). A changing climate is eroding the geographical range of the Namib Desert tree Aloe through population declines and dispersal lags. Diversity Distribution, 13, 645–653.
28. Gerard, P. R., Fernández-Manjarrés, J. F. and Frascaria-Lacoste, N. (2006a). Temporal cline in a hybrid zone population between Fraxinus excelsior L. and Fraxinus angustifolia Vahl. Molecular Ecology, 15, 3655–3667.
29. Gerard, P. R., Klein, E. K., Austerlitz, F., Fernández-Manjarrés, J. F. and Frascaria-Lacoste, N. (2006b). Assortative mating and differential male mating success in an ash hybrid zone population. BMC Evolutionary Biology, 6, 96.
30. Gerard, P. R., Fernández-Manjarrés, J. F., Bertolino, P. et al. (2006c). New insights in the recognition of the European ash species Fraxinus excelsior L. and Fraxinus angustifolia Vahl as useful tools for forest management. Annals of Forest Science, 63, 733–738.
31. Giorgi, F., Bi, X. and Pal, J. (2004). Mean interannual and trends in a regional climate change experiment over Europe. II: climate change scenarios (2071–2100). Climate Dynamics, 23, 839–858.
32. Harrison, R. G. (1993). Hybrid Zones and the Evolutionary Process. New York, NY: Oxford University Press.
33. Heuertz, M., Hausman, J. F., Tsvetkov, I., Frascaria-Lacoste, N. and Vekemans, X. (2001). Assessment of genetic structure within and among Bulgarian populations of the common ash (Fraxinus excelsior L.). Molecular Ecology, 10, 1615–1623.
34. Heuertz, M., Hausman, J. F., Hardy, O. J. et al. (2004). Nuclear microsatellites reveal contrasting patterns of genetic structure between western and southeastern European populations of the common ash (Fraxinus excelsior L.). Evolution, 58, 976–988.
35. Heuertz, M., Carnevale, S., Fineschi, S. et al. (2006). Chloroplast DNA phylogeography of European ashes, Fraxinus sp. (Oleaceae): roles of hybridization and life history traits. Molecular Ecology, 15, 2131–2140.
36. Hewitt, G. (2000). The genetic legacy of the Quaternary ice ages. Nature, 405, 907–913.
37. Hijmans, R. J., Cameron, S. E., Parra, J. L., Jones, P. G. and Jarvis, A. (2005). Very high resolution interpolated climate surfaces for global land areas. International Journal of Climatology, 25, 1965–1978.
38. Hodkinson, T. R., Chase, M. W., Takahashi, C. et al. (2002). The use of DNA sequencing (ITS and trnL-F), AFLP, and fluorescent in situ hybridization to study allopolyploid Miscanthus (Poaceae). American Journal of Botany, 89, 279–286.
39. Horgan, T., Keane, M., Mccarthy, R., Lally, M. and Thompson, D. (2004). A Guide to Forest Tree Species Selection and Silviculture in Ireland. Dublin: COFORD.
40. Howard, D. J. (1999). Conspecific sperm and pollen precedence and speciation. Annual Review of Ecology and Systematics, 30, 109–132.
41. Intergovernmental Panel on Climate Change (IPCC) (2007). Climate Change 2007: Impacts, Adaptation and Vulnerability. Contribution of Working Group II to the FourThassessment Report of the Intergovernmental Panel on Climate Change, ed. M. Parry, O. Canziani, J. Palutikof, P. van der Linden and C. Hanson. Cambridge: Cambridge University Press.
42. Jato, V., Rodriguez-Rajo, F. J., Dacosta, N. and Aira, M. J. (2004). Heat and chill requirements of Fraxinus flowering in Galicia (NW Spain). Grana, 43, 217–223.
43. Jeandroz, S., Frascaria-Lacoste, N. and Bousquet, J. (1996). Molecular recognition of the closely related Fraxinus excelsior and F. oxyphylla (Oleaceae) by RAPD markers. Forest Genetics, 3, 237–242.
44. Jones, P. D. and Moberg, A. (2003). Hemispheric and large scale surface air temperature variations: an extensive revision and an update to 2001. Journal of Climate, 16, 206–223.
45. Jouve, L., Jacques, D., Douglas, G. C., Hoffmann, L. and Hausman, J. F. (2007). Biochemical characterization of early and late bud flushing in common ash (Fraxinus excelsior L.). Plant Science, 172, 962–969.
46. Kelleher, C. T., Hodkinson, T. R., Douglas, G. C. and Kelly, D. L. (2005). Species distinction in Irish populations of Quercus petraea and Q. robur: morphological versus molecular analyses. Annals of Botany, 96, 1237–1246.
47. Khasa, D., Pollefeys, P., Navarro-Quezada, A., Perinet, P. and Bousquet, J. (2005). Species-specific microsatellite markers to monitor gene flow between exotic poplars and their natural relatives in eastern NorThamerica. Molecular Ecology Notes, 5, 920–923.
48. Kuchta, S. R. and Tan, A. M. (2005). Isolation by distance and post-glacial range expansion in the rough-skinned newt, Taricha granulosa. Molecular Ecology, 14, 225–244.
49. Kullman, L. (2008). Early postglacial appearance of tree species in northern Scandinavia: review and perspective. Quaternary Science Reviews, 27, 2467–2472.
50. Lavergne, S., Molina, J. and Debussche, M. (2006). Fingerprints of environmental change on the rare Mediterranean flora: a 115-year study. Global Change Biology, 12, 1466–1478.
51. Leitch, I. J. and Bennett, M. D. (1997). Polyploidy in angiosperms. Trends in Plant Science, 2, 470–476.
52. Lenton, T. M. (2004). The coupled evolution of life and atmospheric oxygen. In Evolution on Planet Earth, ed. L. J. Rothschild and A. Lister. London: Academic Press, pp. 35–53.
53. Levin, D. A. (1978). The origin of isolating mechanisms in flowering plants. Evolutionary Biology, 11, 185–317.
54. Levin, D. A. (2002). The Role of Chromosomal Change in Plant Evolution. Oxford: Oxford University Press.
55. Levin, D. A., Francisco-Ortega, J. and Jansen, R. K. (1996). Hybridization and the extinction of rare plant species. Conservation Biology, 10, 10–16.
56. Lewis, D. and Crowe, L. K. (1958). Unilateral interspecific incompatibility in flowering plants. Heredity, 12, 233–256.
57. Liepelt, S., Cheddadi, R., de Beaulieu, J. L. et al. (2009). Postglacial range expansion and its genetic imprints in Abies alba Mill.: a synthesis from palaeobotanic and genetic data. Review of Palaeobotany and Palynology, 153, 139–149.
58. Lowe, A., Harris, S. and Ashton, P. (2004). Ecological Genetics: Design, Analysis, and Application. Oxford: Blackwell.
59. Mahoney, M. J. (2004). Molecular systematics and phylogeography of the Plethodon elongatus species group: combining phylogenetic and population genetic methods to investigate species history. Molecular Ecology, 13, 149–166.
60. Marigo, G., Peltier, J. P., Girel, J. and Pautou, G. (2000). Success in the demographic expansion of Fraxinus excelsior L. Trees, 15, 1–13.
61. Mebert, K. (2008). Good species despite massive hybridization: genetic research on the contact zone between the watersnakes Nerodia sipedon and N. fasciata in the Carolinas, USA. Molecular Ecology, 17, 1918–1929.
62. Menzel, A. and Fabian, P. (1999). Growing season extended in Europe. Nature, 397, 659.
63. Menzel, A., Sparks, T. H., Estrella, N. et al. (2006). European phenological response to climate change matches the warming pattern. Global Change Biology, 12, 1969–1976.
64. Morand-Prieur, M. E., Brachet, S., Rossignol, P., Dufour, J. and Frascaria-Lacoste, N. (2002). A generalized heterozygote deficiency assessed with microsatellites in French common ash populations. Molecular Ecology, 11, 377–385.
65. Oddo, E., Saiano, F., Alonzo, G. and Bellini, E. (2002). An investigation of the seasonal pattern of mannitol content in deciduous and evergreen species of the Oleaceae growing in northern Sicily. Annals of Botany, 90, 239–243.
66. Otto, S. P. and Whitton, J. (2000). Polyploid incidence and evolution. Annual Review of Genetics, 34, 401–437.
67. Parmesan, C. (2006). Ecological and evolutionary responses to recent climate change. Annual Review of Ecology, Evolution, and Systematics, 37, 637–669.
68. Parmesan, C. and Yohe, G. (2003). A globally coherent fingerprint of climate change impacts across natural systems. Nature, 421, 37–42.
69. Parmesan, C., Gaines, S., Gonzalez, L. et al. (2005). Empirical perspectives on species borders: from traditional biogeography to global change. Oikos, 108, 58–75.
70. Pascarella, J. B. (2007). Mechanisms of prezygotic reproductive isolation between two sympatric species, Gelsemium rankinii and G. sempervirens (Gelsemiaceae), in the southeastern United States. American Journal of Botany, 94, 468–476.
71. Patonnier, M. P., Peltier, J. P. and Marigo, G. (1999). Drought-induced increase in xylem malate and mannitol concentrations and closure of Fraxinus excelsior L. stomata. Journal of Experimental Botany, 50, 1223–1229.
72. Pauli, H., Gottfried, M., Reiter, K., Klettner, C. and Grabherr, G. (2006). Signals of range expansions and contractions of vascular plants in the high Alps: observations (1994–2004) at the GLORIA master site Schrankogel, Tyrol, Austria. Global Change Biology, 13, 147–156.
73. Perron, M. and Bousquet, J. (1997). Natural hybridization between black spruce and red spruce. Molecular Ecology, 6, 725–734.
74. Phillips, S. J., Anderson, R. P. and Schapire, R. E. (2006). Maximum entropy modeling of species geographic distributions. Ecological Modelling, 190, 231–259.
75. Picard, J. F. (1983). A propos du frêne oxyphylle, Fraxinus angustifolia Vahl. Forêt-Entreprise, 83, 2–4.
76. Räisänen, J., Hansson, U., Ullerstig, A. et al. (2004). European climate in the late 21st century: regional simulations with two driving global models and two forcing scenarios. Climate Dynamics, 22, 13–31.
77. Rameau, J. C., Mansion, D. and Dumé, G. (1989). Flore forestière Française, guide écologique illustré. Paris: Institut pour le Développement Forestier.
78. Ramsey, J. and Schemske, D. W. (2002). Neopolyploidy in flowering plants. Annual Review of Ecology and Systematics, 33, 589–639.
79. Raquin, C., Jung-Muller, B., Dufour, J. and Frascaria-Lacoste, N. (2002). Rapid seedling obtaining from European ash species Fraxinus excelsior L. and Fraxinus angustifoli a Vahl. Annals of Forest Sciences, 59, 219–224.
80. Rathcke, B. and Lacey, E. P. (1985). Phenological patterns of terrestrial plants. Annual Review of Ecology and Systematics, 16, 179–214.
81. Raybould, A. F. and Gray, A. J. (1994). Will hybrids of genetically modified crops invade natural communities? Trends in Ecology and Evolution, 9, 85–89.
82. Rhymer, J. M. and Simberloff, D. (1996). Extinction by hybridization and introgression. Annual Review of Ecology and Systematics, 27, 83–109.
83. Rieseberg, L. H. (1997). Hybrid origins of plant species. Annual Review of Ecology and Systematics, 28, 359–389.
84. Rieseberg, L. H. (2006). Hybrid speciation in wild sunflowers. Annals of Missouri Botanical Garden, 93, 34–48.
85. Rieseberg, L. H. and Burke, J. M. (2001). The biological reality of species: gene flow, selection, and collective evolution. Taxon, 50, 47–67.
86. Rieseberg, L. H. and Carney, S. E. (1998). Plant hybridization. New Phytologist, 140, 599–624.
87. Rieseberg, L. H. and Willis, J. H. (2007). Plant speciation. Science, 317, 910–914.
88. Rieseberg, L. H., Archer, M. A. and Wayne, R. K. (1999). Transgressive segregation, adaptation and speciation. Heredity, 83, 363–372.
89. Rieseberg, L. H., Raymond, O., Rosenthal, D. M. et al. (2003). Major ecological transitions in wild sunflowers facilitated by hybridization. Science, 301, 1211–1216.
90. Root, T. L., Price, J. T., Hall, K. R., Schneider, S. H. and Rosenzweig, C. (2003). Fingerprints of global warming on wild animals and plants. Nature, 421, 57–60.
91. Root, T. L., Macmynowski, D. P., Mastrandrea, M. D. and Schneider, S. H. (2005). Human-modified temperatures induce species changes: joint attribution. Proceedings of the National Academy of Sciences of the USA, 102, 7465–7469.
92. Ross, C. L. and Harrison, R. G. (2006). Viability selection on overwintering eggs in a field cricket mosaic hybrid zone. Oikos, 115, 53–68.
93. Savolainen, O., Pyhajarvi, T. and Knurr, T. (2007). Gene flow and local adaptation in trees. Annual Review of Ecology, Evolution, and Systematics, 38, 595–619.
94. Schierenbeck, K. A., Symonds, V. V., Gallagher, K. G. and Bell, J. (2005). Genetic variation and phylogeographic analyses of two species of Carpobrotus and their hybrids in California. Molecular Ecology, 14, 539–547.
95. Schluter, D. (2001). Ecology and the origin of species. Trends in Ecology and Evolution, 16, 372–379.
96. Schönswetter, P., Stehlik, I., Holderegger, R. and Tribsch, A. (2005). Molecular evidence for glacial refugia of mountain plants in the European Alps. Molecular Ecology, 14, 3547–3555.
97. Seehausen, O. (2004). Hybridization and adaptive radiation. Trends in Ecology and Evolution, 19, 198–207.
98. Soltis, P. S. and Soltis, D. E. (2009). The role of hybridization in plant speciation. Annual Review of Plant Biology, 60, 561–588.
99. Sota, T. and Volger, A. P. (2001). Incongruence of mitochondrial and nuclear gene trees in the Carabid beetles Ohomopterus. Systematic Biology, 50, 39–59.
100. Stace, C. A. (1975). Hybridization and the Flora of the British Isles. London: Academic Press.
101. Taylor, E. B., Boughman, J. W., Groenenboom, M. et al. (2006). Speciation in reverse: morphological and genetic evidence of the collapse of a three-spined stickleback (Gasterosteus aculeatus) species pair. Molecular Ecology, 15, 343–355.
102. Tsukada, M. (1982). Late-Quaternary shift of fagus distribution. Journal of Plant Research, 95, 203–217.
103. Valbuena-Carabanã, M., Gonzàlez- Martinez, S. C., Sork, V. L. et al. (2005). Gene flow and hybridisation in a mixed oak forest (Quercus pyrenaica Willd. and Quercus petraea (Matts.) Liebl.) in central Spain. Heredity, 95, 457–465.
104. van Vliet, A. J. H., de Groot, R. S., Overeem, A., Jacobs, A. F. G. and Spieksma, F. T. M. (2002). The influence of temperature and climate change on the timing of pollen release in the Netherlands. International Journal of Climatology, 22, 1757–1767.
105. Vila, M., Weber, E. and Antonio, C. M. D. (2000). Conservation implications of invasion by plant hybridization. Biological Invasions, 2, 207–217.
106. Visser, M. E. and Holleman, L. J. M. (2001). Warmer springs disrupt the synchrony of oak and winter moth phenology. Proceedings of the Royal Society of London B, 268, 289–294.
107. Vitasse, Y., Delzon, S., Dufrêne, E. et al. (2009). Leaf phenology sensitivity to temperature in European trees: do within-species populations exhibit similar responses? Agricultural and Forest Meteorology, 149, 735–744.
108. Wachowiak, W. and Prus-Glowacki, W. (2008). Hybridisation processes in sympatric populations of pines Pinus sylvestris L., P. mugo Turra and P. uliginosa Neumann. Plant Systematics and Evolution, 271, 29–40.
109. Wagner, W. H. J. (1970). Biosystematics and evolutionary noise. Taxon, 19, 146–151.
110. Wallander, E. and Albert, V. A. (2000). Phylogeny and classification of Oleaceae based on rps16 and trnL-F sequence data1. American Journal of Botany, 87, 1827–1841.
111. Weis, A. E. and Kossler, T. M. (2004). Genetic variation in flowering time induces phenological assortative mating: quantitative genetic methods applied to Brassica rapa. American Journal of Botany, 91, 825–836.
112. White, M. A., Brunsell, N. and Schwartz, M. D. (2003). Vegetation phenology in global change studies. In Phenology: an Integrative Environmental Science, ed. M. D. Schwartz. Dordrecht: Kluwer, pp. 453–466.
113. Winge, Ö. (1917). The chromosomes: their number and general importance. Comptes Rendues des Travaux du Laboratoire Carlesberg, 13, 131–275.
114. Young, A., Boyle, T. and Brown, T. (1996). The population genetic consequences of habitat fragmentation for plants. Trends in Ecology and Evolution, 11, 413–418.