Within-population spatial genetic structure in four naturally fragmented species of a neotropical inselberg radiation, Alcantarea imperialis, A. geniculata, A. glaziouana and A. regina (Bromeliaceae)

Heredity

Volumn 101, Issue 3, 2008, Pages 285-296

  Barbara T ^a   Lexer, C ^a   Martinelli, G ^b   Mayo, S ^c   Fay, M F ^a   Heuertz, M ^d  

^a JODRELL LABORATORY   (United Kingdom)

^b Instituto de Pesquisas   (Brazil)

^c ROYAL BOTANIC GARDENS   (United Kingdom)

^d UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

Author keywords

Alcantarea; Bromeliaceae; Colour morphs; Gene dispersal; Inselberg; Spatial genetic structure

Indexed keywords

MICROSATELLITE DNA; PLANT DNA;

ADAPTIVE RADIATION; COLOR MORPH; GENETIC STRUCTURE; HABITAT FRAGMENTATION; MONOCOTYLEDON; NEOTROPICAL REGION; POLLINATION; POPULATION GENETICS; RAINFOREST; REPRODUCTIVE STRATEGY;

ARTICLE; BRAZIL; BREEDING; BROMELIACEAE; CLASSIFICATION; ECOSYSTEM; GENE FLOW; GENETICS; MOLECULAR EVOLUTION; PIGMENTATION; PLANT SEED; POLLEN; POPULATION GENETICS; SPECIES DIFFERENCE; TROPIC CLIMATE;

BRAZIL; BREEDING; BROMELIACEAE; DNA, PLANT; ECOSYSTEM; EVOLUTION, MOLECULAR; GENE FLOW; GENETICS, POPULATION; MICROSATELLITE REPEATS; PIGMENTATION; POLLEN; SEEDS; SPECIES SPECIFICITY; TROPICAL CLIMATE;

ATLANTIC FOREST; BRAZIL; SOUTH AMERICA;

ALCANTAREA; ALCANTAREA IMPERIALIS; ALCANTAREA REGINA; BROMELIACEAE;

EID: 50049123244     PISSN: 0018067X     EISSN: 13652540     Source Type: Journal    
DOI: 10.1038/hdy.2008.65     Document Type: Article

References (51)

1. Baker HG (1967). Support for Baker's law as a rule. Evolution 21: 853-856.
2. Barbará T (2008). Molecular population genetics of four closely related species of Alcantarea (Bromeliaceae) adopted to inselbergs in the Atlantic Rainforest of Brazil. PhD thesis, Open University, UK.
3. Barbará T, Martinelli G, Fay MF, Mayo SJ, Lexer C (2007). Population differentiation and species cohesion in two closely related plants adapted to neotropical high-altitude 'inselbergs', Alcantarea imperialis and Alcantarea geniculata (Bromeliaceae). Mol Ecol 16: 1981-1992.
4. Barbará T, Martinelli G, Palma-Silva C, Fay MF, Mayo S, Lexer C (in review). Genetic relationships and variation in reproductive strategies in four closely related bromeliads adapted to neotropical 'inselbergs', Alcantarea glaziouana, A. regina, A. geniculata and A. imperialis (Bromeliaceae).
5. Barfuss MHJ, Samuel R, Till W, Stuessy TF (2005). Phylogenetic relationships in subfamily Tillandsioideae (Bromeliaceae) based on DNA sequence data from seven plastid regions. Am J Bot 92: 337-351.
6. Barrett SCH (2003). Mating strategies in flowering plants: the outcrossing-selfing paradigm and beyond. Philos Trans R Soc Lond B 358: 991-1004.
7. Benzing DH (2000). Bromeliaceae: Profile of an Adaptive Radiation. Cambridge University Press: Cambridge.
8. Bittencourt JVM, Sebbenn AM (2007). Patterns of pollen and seed dispersal in a small, fragmented population of the wind-pollinated tree Araucaria angustifolia in southern Brazil. Heredity 99: 580-591.
9. Boneh L, Kuperus P, Van Tienderen PH (2003). Microsatellites in the bromeliads Tillandsia fasciculata and Guzmania monostachya. Mol Ecol Notes 3: 302-303.
10. Bonnet E, Van de Peer Y (2002). zt: a software tool for simple and partial Mantel tests. J Stat Softw 7: 1-12.
11. Byrnes M, Hopper SD (2008). Granite outcrops as ancient islands in old landscapes: evidence from the phylogeography and population genetics of Eucalyptus caesia (Myrtaceae) in Western Australia. Biol J Linn Soc 93: 177-188.
12. Campbell D, Bernatchez L (2004). Genomic scan using AFLP markers as a means to assess the role of directional selection in the divergence of sympatric whitefish ecotypes. Mol Biol Evol 21: 945-956.
13. Charlesworth D (2003). Effects of inbreeding on the genetic diversity of populations. Phil Trans R Soc Lond B 358: 1051-1070.
14. Corander J, Marttinen P (2006). Bayesian identification of admixture events using multilocus molecular markers. Mol Ecol 15: 2833-2843.
15. Doyle J, Doyle J (1987). A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull 19: 1-15.
16. Ennos RA (1994). Estimating the relative rates of pollen and seed migration among plant populations. Heredity 72: 250-259.
17. Epperson BK, Allard RW (1989). Spatial autocorrelation analysis of the distribution of genotypes within populations of lodgepole pine. Genetics 121: 369-377.
18. Fenster CB, Vekemans X, Hardy OJ (2003). Quantifying gene flow from spatial genetic structure data in a metapopulation of Chamaecrista fasciculata (Leguminosae). Evolution 57: 995-1007.
19. Gavrilets S, Vose A (2005). Dynamic patterns of adaptive radiation. Proc Natl Acad Sci USA 102: 18040-18045.
20. Givnish TJ, Sytsma KJ (1997). Molecular Evolution and Adaptive Radiation. Cambridge University Press: Cambridge.
21. Hamrick JL, Murawski DA, Nason JD (1993). The influence of seed dispersal mechanisms on the genetic structure of tropical tree populations. Vegetatio 108: 281-297.
22. Hardy O, Vekemans X (2002). SPAGeDi: a versatile computer program to analyse spatial genetic structure at the individual or population levels. Mol Ecol Notes 2: 618-620.
23. Heuertz M, Vekemans X, Hausman JF, Palada M, Hardy OJ (2003). Estimating seed vs pollen dispersal from spatial genetic structure in the common ash. Mol Ecol 12: 2483-2495.
24. Knowles LL (2001). Did the Pleistocene glaciations promote divergence? Tests of explicit refugial models in montane grasshoppers. Mol Ecol 10: 691-701.
25. Lande R, Schemske DW (1985). The evolution of self-fertilization and inbreeding depression in plants. 1. Genetic models. Evolution 39: 24-40.
26. Loiselle B, Sork V, Nason J, Graham C (1995). Spatial genetic structure of a tropical understory shrub. Am J Bot 82: 1420-1425.
27. Lowe AJ, Boshier D, Ward M, Bacles CFE, Navarro C (2005). Genetic resource impacts of habitat loss and degradation; reconciling empirical evidence and predicted theory for neotropical trees. Heredity 95: 255-273.
28. MacArthur RH, Wilson EO (1967). The Theory of Island Biogeography. Princeton University Press: New Jersey.
29. Martinelli G (1994). Reproductive Biology of Bromeliaceae in the Atlantic Rainforest of Southeastern Brazil, PhD thesis, University of St Andrews: St Andrews.
30. McCauley DE (1997). The relative contributions of seed and pollen movement to the local genetic structure of Silene alba. J Hered 88: 257-263.
31. Murawski DA, Hamrick JL (1990). Local genetic and clonal structure in the tropical terrestrial bromeliad, Aechmea magdalenae. Am J Bot 77: 1201-1208.
32. Paggi GM, Palma-Silva C, Silveira LCT, Kaltchuk-Santos E, Bodanese-Zanettini MH, Bered F (2007). Fertility of Vriesea gigantea Gaud. (Bromeliaceae) in southern Brazil. Am J Bot 94: 683-689.
33. Palma-Silva C, Cavallari MM, Barbará T, Lexer C, Gimenes MA, Bered F et al. (2007). A set of polymorphic microsatellite loci for Vriesea gigantea and Alcantarea imperialis (Bromeliaceae) and cross-amplification in other bromeliad species. Mol Ecol Notes 7: 654-657.
34. Porembski S, Barthlott W (2000). Inselbergs. Biotic Diversity of Isolated Rock Outcrops in Tropical and Temperate Regions. Springer-Verlag: Berlin, Heidelberg, New York.
35. Raymond M, Rousset F (1995). GENEPOP (version 1.2): population genetics software for exact tests and ecumenicism. J Hered 86: 248-249..
36. Sarthou C, Boisselier-Dubayle MC, Lambourdiere J, Samadi S (2003). Polymorphic microsatellites for the study of fragmented populations of Pitcairnia geyskesii L.B. Smith (Bromeliaceae), a specific saxicolous species of inselbergs in French Guiana. Mol Ecol Notes 3: 221-223.
37. Sarthou C, Samadi S, Boisselier-Dubayle MC (2001). Genetic structure of the saxicole Pitcairnia geyskesii (Bromeliaceae) on inselbergs in French Guiana. Am J Bot 88: 861-868.
38. Savolainen V, Anstett MC, Lexer C, Hutton I, Clarkson JJ, Norup MV et al. (2006). Sympatric speciation in palms on an oceanic island. Nature 441: 210-213.
39. Sazima M, Buzato S, Sazima I (1999). Bat-pollinated flower assemblages and bat visitors at two Atlantic forest sites in Brazil. Ann Bot 83: 705-712.
40. Schluter D (2000). The Ecology of Adaptive Radiation. Oxford University Press: Oxford.
41. Schönswetter P, Stehlik I, Holderegger R, Tribsch A (2005). Molecular evidence for glacial refugia of mountain plants in the European Alps. Mol Ecol 14: 3547-3555.
42. Seehausen O (2004). Hybridization and adaptive radiation. Trends Ecol Evol 19: 198-207.
43. Sgorbati S, Labra M, Grugni E, Barcaccia G, Galasso G, Boni U et al. (2004). A survey of genetic diversity and reproductive biology of Puya raimondii (Bromeliaceae), the endangered queen of the Andes. Plant Biol 6: 222-230.
44. Soltis DE, Gilmartin AJ, Rieseberg L, Gardner S (1987). Genetic variation in the epiphytes Tillandsia ionantha and Tillandsia recurvata (Bromeliaceae). Am J Bot 74: 531-537.
45. Stuessy TF, Jakubowsky G, Gomez RS, Pfosser M, Schlü ter PM, Fer T et al. (2006). Anagenetic evolution in island plants. J Biogeogr 33: 1259-1265.
46. Tseng M (2007). Evolution in human-altered environments: a summit to translate science into policy. Mol Ecol 16: 3287-3288.
47. Van Rossum F, Triest L (2007). Fine-scale spatial genetic structure of the distylous Primula veris in fragmented habitats. Plant Biol 9: 374-382.
48. Vaughan S, Cottrell J, Moodley D, Connolly T, Russell K (2007). Distribution and fine-scale spatial-genetic structure in British wild cherry (Prunus avium L. Heredity 98: 274-283.
49. Vekemans X, Hardy OJ (2004). New insights from fine-scale spatial genetic structure analyses in plant populations. Mol Ecol 13: 921-935.
50. Young A, Boyle T, Brown T (1996). The population genetic consequences of habitat fragmentation for plants. Trends Ecol Evol 11: 413-418.
51. Zoro Bi I, Maquet A, Baudoin J-P (1997). Spatial patterns of allozyme variants within three wild populations of Phaseolus lunatus L. from the central valley of Costa Rica. Belg J Bot 129: 149-155.