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Mating Systems of Psychotria tenuinervis (Rubiaceae): Distance from Anthropogenic and Natural Edges of Atlantic Forest Fragment

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Abstract

The aim of this study was to determine and compare the mating systems among Psychotria tenuinervis populations at anthropogenic edges, natural edges, and the forest interior using allozyme electrophoresis of naturally pollinated progeny arrays. P. tenuinervis showed low outcrossing rates, varying from 37% to 50% of the mating attributable to outcrossing and 50% to 63% attributable to self-fertilization, in the three habitats. The forest interior had the highest outcrossing rate (t m = 0.50 and t s = 0.43) among the three habitats. However, there were no differences in either multilocus or single-locus rates among the three habitats, indicating that the contribution of biparental inbreeding to the apparent selfing rate in these populations was very low. The multilocus (t m) and single-locus (t s) outcrossing rates for the P. tenuinervis in the sample plots within each habitat showed great heterogeneity. In conclusion, edge creation seems not to influence its mating systems. Additionally, although P. tenuinervis is a distylous species, the population’s inbreeding can be attributed almost entirely to self-fertilization.

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References

  • Aizen MA, Feinsinger P (1994) Forest fragmentation, pollination, and plant reproduction in a chaco dry forest, Argentina. Ecology 75:330–351

    Article  Google Scholar 

  • Barrett SCH (1977) Tristyly in Eichhornia crassipes (Mart.) Solms. (water hyacinth). Biotropica 9:230–239

    Article  Google Scholar 

  • Barrett SCH (1979) The evolutionary breakdown of tristyly in Eichhornia crassipes (Mart.) Solms. (water hyacinth). Evolution 33:499–510

    Article  Google Scholar 

  • Barrett SCH, Husband BC (1990) Variation in outcrossing rates in Eichhornia paniculata: the role of demographic and reproductive factors. Plant Spec Biol 5:41–55

    Article  Google Scholar 

  • Barroso GM (1991) Sistemática de Angiospermas do Brasil. Imprensa Universitária, Universidade Federal de Viçosa, Viçosa

    Google Scholar 

  • Bawa KS, Beach JH (1983) Self-incompatibility systems in the Rubiaceae of a tropical lowland wet forest. Am J Bot 70:1281–1288

    Article  Google Scholar 

  • Broadhurst L, Young A (2007) Seeing the wood and the trees: predicting the future for fragmented plant populations in Australian landscapes. Austr J Bot 55:250–260

    Article  Google Scholar 

  • Castric V, Vekemans X (2004) Plant self-incompatibility in natural populations: a critical assessment of a recent theoretical and empirical advances. Mol Ecol 13:2873–2889

    Article  PubMed  CAS  Google Scholar 

  • Coates VJ, Hamley VL (1999) Genetic divergence and the mating system in the endangered and geographically restricted species Lambertia orbifolia Gardner (Proteaceae). Heredity 83:418–427

    Article  PubMed  Google Scholar 

  • Coates DJ, Sampson JF, Yates CJ (2007) Plant mating systems and assessing population persistence in fragmented landscapes. Austr J Bot 55:239–249

    Article  Google Scholar 

  • Corbet SA (1990) Pollination and the weather. Israel J Bot 39:13–30

    Google Scholar 

  • Ellstrand NC, Elam DR (1993) Population genetic consequences of small population size: implications for plant conservation. Ann Rev Ecol Syst 24:217–242

    Article  Google Scholar 

  • Frankel OH, Brown AHD, Burdon JJ (1995) The conservation of plant biodiversity. Cambridge University Press, Cambridge

    Google Scholar 

  • Gomes DMS, Mantovani A, Vieira RC (1995) Anatomia foliar de Psychotria tenuinervis Muell. Arg. e Psychotria stenocalix Muell. Arg. (Rubiaceae). Arqu Biol Technol 38:15–33

    Google Scholar 

  • Hall P, Orrell LC, Bawa KS (1994) Genetic diversity and mating system in a tropical tree, Carapa guianensis (Meliaceae). Am J Bot 81:1104–1111

    Article  Google Scholar 

  • Hamilton CW (1990) Variations on a distylous theme in a mesoamerican Psychotria subgenus Psychotria (Rubiaceae). Mem NY Bot Gard 55:62–75

    Google Scholar 

  • Hamrick JL, Godt MJW (1990) Allozyme diversity in plant species. In: Brown AHD, Clegg MT, Kahler AL, Weir BS (eds). Plant population genetics, breeding and genetic resources. Sinauer Associates, Sunderland, pp 43–63

    Google Scholar 

  • Hobbs RJ, Yates CJ (2003) Turner Review No. 7. Impact of ecosystems fragmentation on plant populations: generalizing the idiosyncratic. Austr J Bot 51:471–488

    Article  Google Scholar 

  • Jain SK (1976) The evolution of inbreeding in plants. Ann Rev Ecol Syst 7:469–495

    Article  Google Scholar 

  • Lee SL (2000) Mating systems parameters Dryobalanops aromatica Gaertn. f. (Dipterocarpaceae) in three different forest types and seed orchads. Heredity 85:338–345

    Article  PubMed  Google Scholar 

  • Leimu R, Mutikainen P, Koricheva J, Fischer M (2006) How general are positive relationships between plant population size, fitness and genetic variation. J Ecol 94:942–952

    Article  Google Scholar 

  • Loiselle BA, Sork VL, Nason J, Graham C (1995) Spatial genetic structure of a tropical understory shrub, Psychotria officinalis (Rubiaceae). Am J Bot 82:1420–1425

    Article  Google Scholar 

  • Lott RH, Jackes BR (2001) Isozyme analysis of rain forest plants using immature seeds. Biotropica 33:197–204

    Google Scholar 

  • Mattlack GR (1994) Vegetation dynamics of the forest edge: trends in space and sucessional time. J Ecol 82:113–123

    Article  Google Scholar 

  • Murawski DA, Hamrick JL (1992) Mating system and phenology of Ceiba pentandra (Bombacaceae) in Central Panama. J Hered 83:401–404

    Google Scholar 

  • Murcia C (1995) Edge effects in fragmented forests: implications for conservation. Trend Ecol Evol 10:58–62

    Article  Google Scholar 

  • O’Connell LM, Mosseler A, Rajora OP (2006) Impacts of forest fragmentation on the mating system and genetic diversity of white spruce (Picea glauca) at the landscape level. Heredity 97:418–426

    Article  PubMed  CAS  Google Scholar 

  • Paz H, Mazer SJ, Martinez-Ramos M (1999) Seed mass, seedling emergence and environmental factors in seven rain forest Psychotria (Rubiaceae). Ecology 80:1594–1606

    Google Scholar 

  • Perez-Nasser N, Eguiarte LE, Pinero D (1993) Mating system and genetic structure of the distylous tropical tree Psychotria faxlucens (Rubiaceae). Am J Bot 80:45–52

    Article  Google Scholar 

  • Radambrasil (1983) Levantamento de recursos naturais. v.32. Projeto Radambrasil. Rio de Janeiro

  • Ramos FN, Santos FAM (2005) Phenology of Psychotria tenuinervis (Rubiaceae) in Atlantic forest fragments: fragment and habitat scale. Can J Bot 83:1305–1316

    Article  Google Scholar 

  • Ramos FN, Santos FAM (2006a) Floral visitors and pollination of Psychotria tenuinervis (Rubiaceae): distance from the anthropogenic and natural edges of an Atlantic forest fragment. Biotropica 38:1–7

    Article  Google Scholar 

  • Ramos FN, Santos FAM (2006b) Microclimate of Atlantic forest fragments: Regional and local scale heterogeneity. Braz Arch Biol Tech 49:935–944

    Google Scholar 

  • Ramos FN, José J, Solferini VN, Santos FAM (2007) Quality of seeds produced by Psychotria tenuinervis (Rubiaceae): distance from anthropogenic and natural edges of Atlantic forest fragment. Biochem Genet 45:441–458

    Article  PubMed  CAS  Google Scholar 

  • Ribeiro RC, Lovato MB (2004) Mating system in a neotropical tree species, Senna multijuga (Fabaceae). Gen Mol Biol 27:418–424

    Google Scholar 

  • Ritland K (1989) Correlated matings in the partial selfer Mimulus guttatus. Evolution 43:848–859

    Article  Google Scholar 

  • Ritland K (1990) A series of Fortran computer programs for estimating plant mating systems. J Hered 81:235–237

    Google Scholar 

  • Ritland K (2002) Extension of models for the estimation of mating systems using n independent loci. Heredity 88:221–228

    Article  PubMed  Google Scholar 

  • Ritland K, Jain SK (1981) A model for the estimation of outcrossing rate and gene frequencies using n independent loci. Heredity 47:35–52

    Google Scholar 

  • Routley MB, Mavraganis K, Eckert CG (1999) Effect of population size on the mating system in a self-compatible, autogamous plant, Aquilegia canadensis (Ranunculaceae). Heredity 82:518–528

    Article  PubMed  Google Scholar 

  • Saunders DA, Hobbs RJ, Margules CR (1991) Biological consequences of ecosystem fragmentation: a review. Cons Biol 5:18–32

    Article  Google Scholar 

  • Sobrevila C, Ramirez N, Enrech NX (1983) Reproductive biology of Palicourea fendleri and P. petiolaris (Rubiaceae), heterostylous shrubs of tropical cloud forest of Venezuela. Biotropica 15:161–169

    Article  Google Scholar 

  • Soltis DE, Haufler CH, Darrow DC, Gastony GJ (1983) Starch gel electrophoresis of ferns: a compilation of grinding buffers, gel and electrode buffers and stained schedules. Am Fern J 73:9–27

    Article  Google Scholar 

  • Sun M, Ganders FR (1990) Outcrossing rates and allozyme variation in rayed and rayless morphs of Bidens pilosa. Heredity 64:139–143

    Google Scholar 

  • Valladares F, Wright SJ, Lasso E, Kitajima K, Pearcy RW (2000) Plastic phenotypic response to light of 16 congeneric shrubs from a Panamanian rainforest. Ecology 81:1925–1936

    Article  Google Scholar 

  • Vasek FV, Harding J (1976) Outcrossing in natural ppoulations, 5: analysis of outcrossing, inbreeding, and selection in Clarkia exilis and Clarkia tembloriensis. Evolution 30:403–411

    Article  Google Scholar 

  • Veanello RB, Alvez AR (1991) Meteorologia básica e aplicações. Universidade Federal de Viçosa, Viçosa

  • Virillo CB, Ramos FN, Castro CC, Semir J (2007) Floral biology and breeding system of Psychotria tenuinervis Muell.Arg. (Rubiaceae) in the Atlantic rain forest, SE Brazil. Acta Bot Bras 21:879–884

    Google Scholar 

  • Ward M, Dick CW, Gribel R, Lowe AJ (2005) To self, or not to self. A review of outcrossing and pollen-mediated gene flow in neotropical trees. Heredity 95:246–254

    Article  PubMed  CAS  Google Scholar 

  • Ward RD, Warwick T (1980) Genetic differentiation in the molluscan species Littorina rudis and Littorina arcana (Prosobranchia-Littorinidae). Biol J Linn Soc 14:417–428

    Article  Google Scholar 

  • Waser NM, Price MV (1991) Outcrossing distance effects in Delphinium nelsonii: pollen loads, pollen tubes, and seed set. Ecology 72:171–179

    Article  Google Scholar 

  • Washitani I, Oswa R, Namai H, Niva M (1994) Patterns of female fertility in heterostylous Primula sieboldii under severe pollinator limitation. J Ecol 82:571–579

    Article  Google Scholar 

  • Young AG, Boyle TJB, Brown T (1996) The population genetic consequences of habitat fragmentation for plants. TREE 11:413–417

    Google Scholar 

  • Young AG, Brown AHD, Murray BG, Thrall PH, Miller C (2000) Genetic erosion, restricted mating and reduced viability in fragmented populations of the endangered grassland herb Rutiodsis leptorrhynchoides. In: Young AG, Clarke GM (eds) Genetics, demography and viability of fragmented populations. Cambridge University Press, Cambridge, pp 335–359

    Google Scholar 

Download references

Acknowledgments

The authors thank Vanessa Rosseto, Maíra T. Ribeiro, and Carolina B. Virillo for help with the field work, and Aluana G. Abreu and Sónia C. S. Andrade for help in the laboratory. We also thank Aluana G. Abreu, Fabio R. Scarano, Flavia F. Jesus, and Keith S. Brown Jr. for valuable comments on the manuscript. This work was supported by grant 141569/2000-0 from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and research aid 2001/11225-6 from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) and Proap-Capes. F. A. M. Santos was supported by a grant from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, grant 207132/2004-8).

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Correspondence to Flavio Nunes Ramos.

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Ramos, F.N., Zucchi, M.I., Solferini, V.N. et al. Mating Systems of Psychotria tenuinervis (Rubiaceae): Distance from Anthropogenic and Natural Edges of Atlantic Forest Fragment. Biochem Genet 46, 88–100 (2008). https://doi.org/10.1007/s10528-007-9132-8

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