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Comparison of mating system parameters and genetic structure in three natural scenarios of Acacia visco (Leguminosae, Mimosoideae)

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Abstract

Acacia visco is a native South American tree species that has been extensively used for ornamental purposes and in carpentry, bodywork and parquet due to the hardness and durability of its wood. Little is known about genetic diversity and mating system of A. visco. The main aims of this study were to (1) estimate outcrossing rates in natural Argentinean populations using AFLP markers, (2) test for any difference in mating patterns among a large a patchy and relict population, and (3) compare the mating system of A. visco with other Acacia species. The three primer pairs used in the AFLP analysis revealed a total of 569 variable loci. Most genetic variation was observed among individuals within families (61.2 %). The estimate of multilocus outcrossing rate (t m) was high (≥0.971) in all populations. Average pairwise coancestry between progenies within families for each population ranged from 0.082 to 0.105 or from 0.125 to 0.136, depending on the method θ was estimated. In the three populations studied, the progenies of open pollination were constituted mainly for half-sibs (94.3 %). This work shows a similar mating system in all populations of A. visco in spite of their size differences, hypothesizing that the entire species has a similar mating system of outcrossing preferential. Considering the results obtained here where a high percentage of individuals were half-sibs, sampling large numbers of pods from individual trees for ex situ conservation will result in a genetically diverse sample as a consequence of high outcrossing rates.

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References

  • Ali SI, Qaiser M (1980) Hybridization in Acacia nilotica (Mimosoideae) complex. Bot J Linn Soc 80:69–77

    Article  Google Scholar 

  • Barrett SCH, Kohn JR (1991) Genetic and evolutionary consequences of small population size in plants: implications for conservation. In: Falk DA, Holsinger KE (eds) Genetics and conservation of rare plants. Oxford University Press, New York, pp 3–30

    Google Scholar 

  • Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Series B 57:289–300

    Google Scholar 

  • Bernhardt P, Kenrick J, Knox RB (1984) Pollination biology and the breeding system of Acacia retinodes (Leguminosae: Mimosoideae). Ann Mo Bot Gard 71:17–29

    Article  Google Scholar 

  • Bittencourt JM, Sebbenn AM (2008) Pollen movement within a continuous forest of wind-pollinated Araucaria angustifolia, inferred from paternity and TWOGENER analysis. Conserv Genet 9:855–868

    Article  Google Scholar 

  • Casiva PV, Vilardi JC, Cialdella AM, Saidman BO (2004) Mating system and population structure of Acacia aroma and A. macracantha (Fabaceae). Am J Bot 91(1):58–64

    Article  PubMed  Google Scholar 

  • Chiveu Chemulanga J, Dangasuk OG, Omunyin ME, Wachira FN (2008) Genetic diversity in Kenyan populations of Acacia senegal (L.) Willd revealed by combined RAPD and ISSR markers. Afr J Biotechnol 7(14):2333–2340

    Google Scholar 

  • Cialdella AM (1984) El género Acacia (Leguminosae) en la Argentina. Darwiniana 25(1–4):59–11, f. 1–8

  • Clegg MT (1980) Measuring plant mating systems. Bioscience 30:814–818

    Article  Google Scholar 

  • Coates D, Tischler G, McComb JA (2006) Genetic variation and the mating system in the rare Acacia sciophanes compared with its common sister species Acacia anfractuosa (Mimosaceae). Conserv Genet 7:931–944

    Article  Google Scholar 

  • Cockerham CC (1969) Variance of gene frequencies. Evolution 23:72–84

    Article  Google Scholar 

  • Covas G, Schnack B (1946) Número de cromosomas en Antófitas de la Región de Cuyo (República Argentina). Rev Argen Agronom 13:153–166

    Google Scholar 

  • DeMauro MM (1993) Relationship of breeding system to rarity in the lakeside daisy (Hymenoxys acaulis var. glabra). Conserv Biol 7:542–550

    Article  Google Scholar 

  • EnnoS RA, Clegg MT (1982) Effect of population substructuring on estimates of outcrossing rate in plant populations. Heredity 48:283–292

    Article  Google Scholar 

  • Fernández OA, Busso CA (1997) Arid and semi-arid rangelands: two thirds of Argentina. RALA Report: 200

  • Fleming PA, Hofmeyr SD, Nicolson SW (2007) Role of insects in the pollination of Acacia nigrescens (Fabaceae). S Afr J Bot 73(1):49–55

    Article  Google Scholar 

  • Frankham R (1995) Conservation genetics. Annu Rev Genet 29:305–327

    Article  PubMed  CAS  Google Scholar 

  • Freitas MLM, Sebbenn AM, Moraes MLT, Lemos EGM (2004) Mating system of a population of Myracroudon urundeuva F. F. & M. F. Allemão using the fAFLP molecular marker. Genet Mol Biol 27(3):425–431

    Article  CAS  Google Scholar 

  • Gaiotto FA, Bramucci M, Grattapaglia D (1997) Estimation of outcrossing rate in a breeding population of Eucalyptus urophylla with dominant RAPD and AFLP markers. Theor Appl Genet 95:842–849

    Article  CAS  Google Scholar 

  • Gjuric R, Smith SR (1996) Identification of cross-pollinated and selfpollinated progeny in Alfalfa through RAPD nulliplex loci analysis. Crop Sci 36:389–393

    Article  Google Scholar 

  • Goudet J (2005) Hierfstat, a package for R to compute and test hierarchical F-statistics. Mol Ecol Notes 5:184–186. http://www.unil.ch/popgen/softwares/hierfstat.htm

  • Goudet J, Raymond M, DeMeeus T, Rousset F (1995) Testing differentiation in diploid populations. Genetics 144:1933–1940

    Google Scholar 

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

    Article  Google Scholar 

  • Hamrick JL (2004) Response of forest tree to global environmental changes. Forest Ecol Manag 197:323–335

    Article  Google Scholar 

  • Hardy O, Vekemans X (2002) SPAGeDI: a versatile computer program to analyze spatial genetic structure at the individual or population levels. Mol Ecol Notes 2:618–620

    Article  Google Scholar 

  • IUCN 2009 (2009) IUCN Red List of Threatened Species. http://www.iucnredlist.org/details/full/34360/0

  • Jump AS, Penuelas J (2006) Genetic effects of chronic habitat fragmentation in a wind-pollinated tree. P Natl Acad Sci USA 103:8096–8100

    Article  CAS  Google Scholar 

  • Kenrick J, Knox RB (1982) Function of the polyad in reproduction of Acacia. Ann Bot 50:721–727

    Google Scholar 

  • Kenrick J, Knox RB (1985) Self-incompatibility in the nitrogen-fixing tree, Acacia retinodes: quantitative cytology of pollen tube growth. Theor Appl Genet 69:481–488

    Article  Google Scholar 

  • Kenrick J, Knox RB (1989) Quantitative analysis of selfincompatibility in trees of seven species of Acacia. J Hered 80:240–245

    Google Scholar 

  • Kenrick J, Kaul V, Williams EG (1986) Self-incompatibility in Acacia retinodes: site of pollen-tube arrest in the nucellus. Planta 169:245–250

    Article  Google Scholar 

  • Krauss SL (2000) Patterns of mating in Persoonia mollis (Proteaceae) revealed by an analysis of paternity using AFLP: implications for conservation. Aust J Bot 48:349–356

    Article  Google Scholar 

  • Lee SL, Wickneswari R, Mahani MC, Zakri AH (2000) Mating system parameters in a tropical tree species, Shorea leprosula Miq. (Dipterocarpaceae), from Malaysian lowland dipterocarp forest. Biotropica 32(4a):693–702

    Google Scholar 

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

    Article  Google Scholar 

  • Loveless MD (1992) Isozyme variation in tropical trees: patterns of genetic organization. New For 6:67–94

    Article  Google Scholar 

  • Loveless MD, Hamrick JL, Foster RB (1998) Population structure and mating system in Tachigali versicolor, a monocarpic neotropical tree. Heredity 81:134–143

    Article  Google Scholar 

  • Lynch M, Walsh B (1998) Genetics and analyses of quantitative traits. Sinauer, Sunderland

    Google Scholar 

  • Mandal AK, Ennos RA (1995) Mating system analysis in a natural population of Acacia nilotica subspecies kraussiana. Forest Ecol Manag 79:235–240

    Article  Google Scholar 

  • Mandal AK, Ennos RA, Fagg CW (1994) Mating system analysis in a natural population of Acacia nilotica subspecies leiocarpa. Theor Appl Genet 89(7–8):931–935

    Google Scholar 

  • Millar MA, Byrne M, Nuberg I, Sedgley M (2008) High outcrossing and random pollen dispersal in a planted stand of Acacia saligna subsp. saligna revealed by paternity analysis using microsatellites. Tree Genet Genomes 4:367–377

    Article  Google Scholar 

  • Moran GF, Muona O, Bell JC (1989) Breeding systems and genetic diversity in Acacia auriculiformis and Acacia crassicarpa. Biotropica 21:250–256

    Article  Google Scholar 

  • Muluvi GM, Sprent JI, Odee D, Powell W (2004) Estimates of outcrossing rates in Moringa oleifera using Amplified fragment length polymorphism (AFLP). Afr J Biotechnol 3(2):146–151

    Google Scholar 

  • Muona O, Moran GF, Bell JC (1991) Hierarchical patterns of correlated mating in Acacia melanoxylon. Genetics 127:619–626

    PubMed  CAS  Google Scholar 

  • Murawski DA, Hamrick JL (1991) The effect of the density of flowering individuals on the mating systems of nine tropical tree species. Heredity 67:167–174

    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 

  • Newman D, Pilson D (1997) Increased probability of extinction due to decreased genetic effective population size: experimental populations of Clarkia pulchella. Evolution 51:354–362

    Article  Google Scholar 

  • Omondi SF, Kireger E, Dangasuk OG, Chikamai B, Odee DW, Cavers S, Khasa DP (2010) Genetic diversity and population structure of Acacia senegal (L) Willd in Kenya. Trop Pl Biol 3:59–70

    Article  Google Scholar 

  • Pedernera AM, Garcia Aseff S, Guardia T, Guardia Calderón CE, Pelzer LE (2007) Study of acute toxicity of Acacia visco methanolic extract in mice argentine society of experimental pharmacology (Sociedad Argentina de Farmacología Experimental), abstracts from the XXXVIII ANNUAL SCIENTIFIC MEETING November 1–3, 2006. Biocell 31(1):75–112

    Google Scholar 

  • Pedernera AM, Guardia T, Calderón CE, Rotelli AE, de la Rocha NE, Saad JR, Verrilli MA, Aseff SG, Pelzer LE (2010) Anti-inflammatory effect of Acacia visco extracts in animal models. Inflammopharmacology 18(5):253–260

    Article  PubMed  Google Scholar 

  • Pometti CL, Vilardi JC, Saidman BO (2011) Mating system parameters and genetic structure in Argentinean populations of Acacia caven (Leguminosae, Mimosoideae). Plant Syst Evol 292:25–32

    Article  Google Scholar 

  • Pometti CL, Bessega CF, Vilardi JC, Saidman BO (2012) Landscape genetic structure of natural populations of Acacia caven in Argentina. Tree Genet Genomes 8(4):911–924

    Article  Google Scholar 

  • R: A Language and Environment for Statistical Computing (2011) R Development Core Team, R Foundation for Statistical Computing, Vienna, Austria, ISBN 3-900051-07-0. http://www.R-project.org

  • Ribeiro RA, Lovato MB (2004) Mating system in a neotropical tree species, Senna multijuga (Fabaceae). Genet Mol Biol 27(3):418–424

    Article  Google Scholar 

  • Ritland K (1983) Estimation of mating systems. In: Tanksley SD, Orton TJ (eds) Isozyme in plant genetics and breeding, part A. Elsevier, Amsterdam, pp 289–302

    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 (1996) Estimators for pairwise relatedness and individual inbreeding coefficients. Genet Resour 67:175–185

    Article  Google Scholar 

  • Ritland K (2009) Multilocus mating system program MLTR. Version 3.4. University of British Columbia, Canadá. http://genetics.forestry.ubc.ca/ritland/programs.html

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

    Article  Google Scholar 

  • Saccheri I, Kuussaari M, Kankare M, Vikman P, Fortelius W, Hanski I (1998) Inbreeding and extinction in a butterfly metapopulation. Nature 392:491–494

    Article  CAS  Google Scholar 

  • Saidman BO, Vilardi JC (1993) Genetic variability and germplasm conservation in the genus Prosopis, 187–198. In: Puri S (ed) Nursery technology of forest tree species of arid and semiarid regions. Winrock-Oxford & IBH Publishing Co. PVT. Ltd, New Delhi/Bombay/Calcutta

    Google Scholar 

  • Sebben AM (2006) Sistema de Reproduccion en species arboreas tropicales e suas implicancacoes para la selecao de arvores matrized para reforestamentos ambientais. In: Higa AR, Silva LD (eds) Pomares de sementes en especies forestais nativas. FUPEF, Curitiba, pp 93–138

    Google Scholar 

  • Sedgley M, Harbard J, Smith R-MM, Wickneswari R, Griffin AR (1992) Reproductive biology and interspecific hybridization of Acacia mangium and A. auriculiformis A. Cunn. ex Benth. (Leguminosae: Mimosoideae). Aust J Bot 40:37–48

    Article  Google Scholar 

  • Sobierajski G, Kageyama PY, Sebbenn AM (2006) Mating system in nine Mimosa scabrella Bentham populations (Leguminosaceae). Sci For 71:37–49

    Google Scholar 

  • Sork VL, Smouse PE (2006) Genetic analysis of landscape connectivity in tree populations. Landscape Ecol 21:821–836

    Article  Google Scholar 

  • Sousa VA, Sebbenn AM, Hattemer H, Ziehe M (2005) Correlated mating in populations of a dioecious Brazilian conifer, Araucaria angustifolia (Bert.) O. Ktze. Forest Genet 12:107–119

    Google Scholar 

  • Tortorelli LA (1956) Maderas y bosques Argentinos. Editorial ACME, S.A.C.I., Buenos Aires

  • Vilardi JC, Saidman BO, Palacios RA (1988) Muestreo según variabilidad, 119–124, in Prosopis en Argentina. Documento preliminar elaborado para el I Taller Internacional sobre Recurso genético y conservación de germoplasma en Prosopis. Fac. de Cs. Agropecuarias, UNC-FAO, PIRB

  • Vos P, Hogers R, Bleeker M, Reijans M, van de Lee T, Hornes M, Freijters A, Pot J, Peleman J, Kuiper M, Zabeau M (1995) AFLP: a new technique for DNA fingerprinting. Nucleic Acids Res 23:4407–4414

    Article  PubMed  CAS  Google Scholar 

  • Workman P, Niswander JL (1970) Population studies, on southwestern Indian tribes. II. Local genetic differentiation in the Papago. Am J Hum Genet 22:24–49

    PubMed  CAS  Google Scholar 

  • Wright S (1951) The genetical structure of populations. Ann Eugenics 15:323–354

    Google Scholar 

  • Zanín LA, Cangiano MA, Lossino HN (1998) Números cromosómicos en Acacia (Fabaceae) de la provincia de San Luis, Argentina. Darwiniana 35(1–4):45–48

    Google Scholar 

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Acknowledgments

The authors of this work want to thank Dr. Ana María Cialdella of Instituto de Botánica Darwinion, who kindly determined the material studied here. This work was supported by the Universidad de Buenos Aires (EX20020100100008 to B. O.S.) and the Consejo Nacional de Investigaciones Científicas y Técnicas (PIP 11220090100147 to J. C. V.). A special thanks to the Lic. Ariel Guionet from the SERVICIO DE SECUENCIACIÓN Y GENOTIPIFICADO from Departamento de Ecología Genética y Evolución, FCEyN, UBA.

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Correspondence to Carolina L. Pometti.

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Pometti, C.L., Bessega, C.F., Vilardi, J.C. et al. Comparison of mating system parameters and genetic structure in three natural scenarios of Acacia visco (Leguminosae, Mimosoideae). Plant Syst Evol 299, 761–771 (2013). https://doi.org/10.1007/s00606-013-0759-0

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