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An apparent lack of prezygotic reproductive isolation among 42 sympatric species of Bromeliaceae in southeastern Brazil

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Abstract

The Atlantic rainforest in southeastern Brazil is one the main centers of diversification of Bromeliaceae. Empirical estimates of the relative importance of different pre- and postzygotic barriers to gene flow between recently diverged species are important for understanding speciation processes. While many bromeliad species easily hybridize in cultivation, few records of natural hybrids between closely related sympatric species suggest the existence of strong prezygotic barriers. A community of 42 sympatric bromeliad species, represented by nine genera (Aechmea, Billbergia, Edmundoa, Neoregelia, Nidularium, Quesnelia, Racinaea, Tillandsia, and Vriesea), were surveyed from 2004–2005 to assess the role of microhabitat isolation, phenological isolation and ethological isolation as potential prezygotic barriers. These bromeliads are abundant in the understory and frequently grow densely aggregated in multispecific patches that may facilitate promiscuous pollination. There was a large overlap of flowering periods even between congeneric species. Most species shared a similar assemblage of flower visitors; the hummingbird Rhamphodon naevius was the major visitor for 35 species. Only one putative hybrid was observed. This uncommonness of hybridization is puzzling, given that the prezygotic isolation mechanisms investigated are potentially weak to effectively avoid interspecific pollination.

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References

  • Aizen MA, Vázquez DP (2006) Flowering phenologies of hummingbird plants from the temperate forest of southern South America: is there evidence of competitive displacement? Ecography 29:357–366

    Article  Google Scholar 

  • Bawa KS, Bullock SH, Perry DR, Coville RE, Grayum MH (1985) Reproductive biology of tropical lowland rain forest trees II. Pollination systems. Am J Bot 72:346–356

    Article  Google Scholar 

  • Benzing DH (2000) Bromeliaceae: profile of an adaptative radiation. Cambridge, Cambridge University Press

    Google Scholar 

  • Canela MBF, Sazima M (2003) Aechmea pectinata: a hummingbird-dependent bromeliad with inconspicuous flowers from the rainforest in south-eastern Brazil. Ann Bot 92:731–737

    Article  PubMed  Google Scholar 

  • Chase MW, Fay MF, Savolainen V (2000) Higher level classification in Angiosperms: new insights from the perspective of DNA sequence data. Taxon 49:685–704

    Article  Google Scholar 

  • Costa AF, Wendt T (2007) Bromeliaceae na região de Macaé de Cima, Nova Friburgo, Rio de Janeiro, Brasil. Rodriguésia 58:905–939

    Google Scholar 

  • Coyne JA, Orr HA (2004) Speciation. Sinauer, Sunderland

    Google Scholar 

  • de Sousa LOF, Silva BR, de Sousa RCOS (2003) x Hohenmea, a new natural intergeneric hybrid in the Bromelioideae. J Bromel Soc 53:71–77

    Google Scholar 

  • de Sousa LOF, Wendt T, Brown GK, Tuthill DE, Evans TM (2007) Monophyly and phylogenetic relationships in Lymania (Bromeliaceae: Bromelioideae) based on morphology and chlroplast DNA sequences. Syst Bot 32:264–270

    Article  Google Scholar 

  • Faria APG, Wendt T, Brown GK (2004) Cladistic relationships of Aechmea (Bromeliaceae: Bromelioideae) and allied genera. Ann Miss Bot Gard 91:303–319

    Google Scholar 

  • Feinsinger P, Tiebout HM (1991) Competition among plants sharing hummingbird pollinators: laboratory experiments on a mechanism. Ecology 72:1946–1952

    Article  Google Scholar 

  • Feldman TS (2006) Pollinator aggregative and functional responses to flower density: does pollinator respond to patches of plants accelerate at low-densities? Oikos 114:128–140

    Google Scholar 

  • Fontoura T, Costa A, Wendt T (1991) Preliminary checklist of the Bromeliaceae of Rio de Janeiro state, Brazil. Selbyana 12:5–45

    Google Scholar 

  • Freitas CA, Scarano FR, Biesboer DD (2003) Morphological variation in two facultative epithytic Bromeliads growing on the floor of a swamp forest. Biotropica 35:546–550

    Article  Google Scholar 

  • Freitas CA, Scarano FR, Wendt T (1998) Habitat choice in two facultative epiphytes of the genus Nidularium (Bromeliaceae). Selbyana 19:236–239

    Google Scholar 

  • Freitas L, Galetto L, Sazima M (2006) Pollination by hummingbirds and bees in eight syntopic species and a putative hybrid of Ericaceae in Southeastern Brazil. Plant Syst Evol 258:49–61

    Article  Google Scholar 

  • Gardner CS (1984) Natural hybridization in Tillandsia subgenus Tillandsia. Selbyana 7:380–393

    Google Scholar 

  • Grant V (1981) Plant speciation. Columbia University Press, New York

    Google Scholar 

  • Grant V (1994) Modes and origins of mechanical and ethological isolation in angiosperms. Proc Natl Acad Sci USA 91:3–10

    Article  PubMed  CAS  Google Scholar 

  • Kaehler M, Varassin IG, Goldenberg R (2005) Polinização em uma comunidade de bromélias em Floresta Atlântica alto-montana no Estado do Paraná, Brasil. Rev Bras Bot 28:219–228

    Article  Google Scholar 

  • Kay KM (2006) Reproductive isolation between two closely related hummingbird-pollinated neotropical gingers. Evolution 60:538–552

    PubMed  Google Scholar 

  • Kephart S, Theiss K (2003) Pollinator-mediated isolation in sympatric milkweeds (Asclepias): do floral morphology and insect behavior influence species boundaries? New Phytol 161:265–277

    Article  Google Scholar 

  • Lasso E, Ackerman JD (2004) The flexible breeding system of Werauhia sintenisii, a cloud forest bromeliad from Puerto Rico. Biotropica 36:417–423

    Google Scholar 

  • Levin DA (1971) The origin of reproductive isolating mechanisms in flowering plants. Taxon 20:91–113

    Article  Google Scholar 

  • Levin DA (2006a) The spatial sorting of ecological species: ghost of competition or of hybridization past? Syst Bot 31:8–12

    Article  Google Scholar 

  • Levin DA (2006b) Flowering phenology in relation to adaptive radiation. Syst Bot 31:239–246

    Article  Google Scholar 

  • Luther HE (1984) A hybrid Pitcairnia from Western Ecuador. J Bromel Soc 34:272–274

    Google Scholar 

  • Machado CG, Semir J (2006) Fenologia da floração e biologia floral de bromélias ornitófilas de uma área da Mata Atlântica do Sudeste brasileiro. Rev Bras Bot 29:163–174

    Article  Google Scholar 

  • Martin NH, Willis JH (2007) Ecological divergence associated with mating system causes nearly complete reproductive isolation between sympatric Mimulus species. Evolution 61:68–82

    Article  PubMed  Google Scholar 

  • Martinelli G (1994) Reproductive biology of Bromeliaceae in the Atlantic Rainforest of southern Brazil. PhD Thesis, University of St. Andrews, Scotland

  • Mendes SL, Padovan MP (2000) A Estação Biológica de Santa Lúcia, Santa Teresa, Espírito Santo. Bol Mus Biol Mello Leitão (N. Sér.) 11/12:7–34

    Google Scholar 

  • Moeller DA (2004) Facilitative interactions among plants via shared pollinators. Ecology 85:3289–3301

    Article  Google Scholar 

  • Pascarella JB (2007) Mechanisms of prezygotic reproductive isolation between two sympatric species, Gelsemium rankinii and G. sempervirens (Gelsemiaceae), in the southeastern United States. Am J Bot 94:468–476

    Article  Google Scholar 

  • Sakai S, Kato M, Inoue T (1999) Three pollination guilds and variation in floral characteristics of Bornean gingers (Zingiberaceae and Costaceae). Am J Bot 86:646–658

    Article  PubMed  Google Scholar 

  • Sampaio MC, Picó FX, Scarano FR (2005) Ramet demography of a nurse bromeliad in Brazilian restingas. Am J Bot 92:674–681

    Article  Google Scholar 

  • Tang L-L, Yu Q, Sun J-F., Huang S-Q (2007) Floral traits and isolation of three sympatric Aquilegia species in the Qinling Mountains, China. Plant Syst Evol 267:121–128

    Article  Google Scholar 

  • Van Der Niet T., Johnson SD, Linder HP (2006) Macroevolutionary data suggest a role for reinforcement in pollination system shifts. Evolution 60:1596–1601

    PubMed  Google Scholar 

  • Varassin IG, Sazima M (2000) Recursos de Bromeliaceae utilizados por beija-flores e borboletas em Mata Atlântica no sudeste do Brasil. Bol Mus Biol Mello Leitão (N. Sér.) 11/12:57–70

    Google Scholar 

  • Versieux LM, Wendt T (2006) Checklist of Bromeliaceae of Minas Gerais, Brazil, with notes on taxonomy and endemism. Selbyana 27:107–146

    Google Scholar 

  • Versieux LM, Wendt T (2007) Bromeliaceae diversity and conservation in Minas Gerais state, Brazil. Biodivers Conserv 16:2989–3009

    Article  Google Scholar 

  • Vervaeke I, Wouters J, Londers E, Deroose R, de Proft MP (2004) Morphology of artificial hybrids of Vriesea splendens × Tillandsia cyanea and V. splendens × Guzmania lingulata (Bromeliaceae). Ann Bot Fenn 41:201–208

    Google Scholar 

  • Wendt T, Canela MBF, Faria APG, Rios RI (2001) Reproductive biology and natural hybridization between two endemic species of Pitcairnia (Bromeliaceae). Am J Bot 88:1760–1767

    Article  Google Scholar 

  • Wendt T, Canela MBF, Klein DE, Rios RI (2002) Selfing facilitates reproductive isolation among three sympatric species of Pitcairnia (Bromeliaceae). Plant Syst Evol 232:201–212

    Article  Google Scholar 

  • Wright SJ, Calderon O (1995) Phylogenetic patterns among tropical phenologies. J Ecol 83:937–948

    Article  Google Scholar 

Download references

Acknowledgments

We thank the Brazilian Research Council (CNPq, 690149/01-8) and the United States National Science Foundation (DEB-0129446) for funding; the staff of Museu de Biologia Mello Leitão for logistic support; numerous colleagues for field assistance; R. L. Cazotto and P. R. Silva for help with hummingbirds identification; E. M. C. Leme for help with the identification of Neoregelia species; F. R. Scarano for comments and linguistic advice; an anonymous reviewer for helpful comments; and CNPq for a productivity grant to T. Wendt.

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Wendt, T., Coser, T.S., Matallana, G. et al. An apparent lack of prezygotic reproductive isolation among 42 sympatric species of Bromeliaceae in southeastern Brazil. Plant Syst Evol 275, 31–41 (2008). https://doi.org/10.1007/s00606-008-0054-7

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  • DOI: https://doi.org/10.1007/s00606-008-0054-7

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