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8 - Pollen and seed movement in disturbed tropical landscapes

Published online by Cambridge University Press:  05 July 2014

J. L. Hamrick
Affiliation:
University of Georgia
J. Andrew DeWoody
Affiliation:
Purdue University, Indiana
John W. Bickham
Affiliation:
Purdue University, Indiana
Charles H. Michler
Affiliation:
Purdue University, Indiana
Krista M. Nichols
Affiliation:
Purdue University, Indiana
Gene E. Rhodes
Affiliation:
Purdue University, Indiana
Keith E. Woeste
Affiliation:
Purdue University, Indiana
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Summary

INTRODUCTION

A characteristic of modern landscapes worldwide is that continuous habitats have become, largely due to human activities, mosaics of remnant habitat fragments embedded in an urban or agricultural matrix (see Chapter 9 by Leberg and colleagues). Landscape fragmentation can have distinct ecological (e.g., species extinction), demographic (e.g., lowered reproduction and elevated mortality), and genetic (e.g., less genetic diversity and increased inbreeding) consequences. In northern temperate regions, human impacts on natural landscapes date back several thousand years but, in most tropical landscapes, widespread human disturbance is more recent, with the heaviest impacts occurring during the last fifty years. Disturbance and fragmentation of once continuous habitats can have immediate, short-term, and long-term consequences for the management and conservation of genetic diversity within tropical plant species.

Immediate consequences

Landscape fragmentation has immediate consequences for the levels and distribution of genetic diversity that are not dependent on population genetic processes acting across subsequent generations. Three factors can have immediate effects on the genetic composition of fragmented populations: 1) the proportion of the original population that is removed, 2) the number of individuals that survive in each fragment, and 3) patterns of genetic variation present within natural populations prior to fragmentation (e.g., clusters of related individuals).

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Publisher: Cambridge University Press
Print publication year: 2010

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References

Aldrich, PR (1997) Dispersal and the Scale of Fragmentation in Tropical Tree Populations. Ph.D. Dissertation, The University of Georgia.Google Scholar
Aldrich, PR, Hamrick, JL (1998) Reproductive dominance of pasture trees in a fragmented tropical forest mosaic. Science, 281, 103–105.CrossRefGoogle Scholar
Allard, RW (1988) Genetic changes associated with the evolution of adaptedness in cultivated plants and their wild progenitors. Journal of Heredity, 79, 225–238.CrossRefGoogle ScholarPubMed
Apsit, VJ (1998) Fragmentation and Pollen Movement in a Costa Rican Dry Forest Tree Species. Ph.D. Dissertation, The University of Georgia.Google Scholar
Bawa, KS (1974). Breeding systems of tree species of a lowland tropical community. Evolution, 28, 85–92.CrossRefGoogle ScholarPubMed
Born, C, Hardy, OJ, Chavallier, MH et al. (2008) Small-scale spatial genetic structure in the Central African rainforest tree species, Aucoumea klaineana: a stepwise approach to infer the impact of limited gene dispersal, population history, and habitat fragmentation. Molecular Ecology, 17, 2041–2050.CrossRefGoogle ScholarPubMed
Boshier, DH, Chase, M, Bawa, KS (1995) Population genetics of Cordia alliodora (Boraginaceae), a neotropical tree. 3: Gene flow, neighborhood, and population substructure. American Journal of Botany, 82, 484–490.CrossRefGoogle Scholar
Cespedes, M, Gutierrez, MV, Halbrook, NM, Roche, OJ (2003) Restoration of genetic diversity in the dry forest tree, Swietenia macrophylla (Meliaceae), after pasture abandonment in Costa Rica. Molecular Ecology, 12, 3201–3212.CrossRefGoogle Scholar
Chase, MR, Moller, C, Kesseli, R, Bawa, KS (1996) Distant gene flow in tropical trees. Nature, 383, 398–399.CrossRefGoogle Scholar
Dawson, IK, Waugh, R, Simons, AJ, Powell, W (1997) Simple sequence repeats provide a direct estimate of pollen-mediated gene dispersal in the tropical tree, Gliricidia sepium. Molecular Ecology, 6, 179–183.CrossRefGoogle Scholar
de Lacerda, AEB, Kanashiro, M, Sebbenn, M (2008) Long-pollen movement and deviation of random mating in a low-density continuous population of a tropical tree, Hymenaea courbaril, in the Brazilian Amazon. Biotropica, 40, 462–470.Google Scholar
Devlin, B, Roeder, K, Ellstrand, N (1988) Fractional paternity assignment: theoretical development and comparisons to other methods. Theoretical and Applied Genetics, 76, 369–380.CrossRefGoogle Scholar
Dick, C (2001a) Habitat change, African honeybees and fecundity in the Amazonian tree, Dinizia excelsa (Fabaceaea). In: Lessons from Amazonia: The Ecology and Conservation of a Fragmented Tropical Forest (eds. Bierregaard, RO, Gascon, C, Lovejoy, TE, Mesquita, R), pp. 146–157. Yale University Press, New Haven, CT.Google Scholar
Dick, CW (2001b) Genetic rescue of remnant tropical trees by an alien pollinator. Proceedings of the Royal Society of London-Series B: Biological Sciences, 28, 2391–2396.CrossRefGoogle Scholar
Dick, CW, Abdul-Salim, K, Bermingham, E (2003) Molecular systematics reveals cryptic tertiary diversification of a widespread tropical rainforest tree. American Naturalist, 162, 691–703.CrossRefGoogle Scholar
Dick, CW, Hardy, OJ, Jones, FA, Petit, RJ (2008) Spatial scales of pollen and seed-mediated gene flow in tropical rainforest trees. Tropical Plant Biology, 1, 20–33.CrossRefGoogle Scholar
Dunphy, BK, Hamrick, JL (2007) Estimation of gene flow into fragmented populations of Bursera simaruba (Burseraceae) in the dry-forest life zone of Puerto Rico. American Journal of Botany, 94, 1786–1794.CrossRefGoogle ScholarPubMed
Dunphy, BK, Hamrick, JL, Scwagerl, J (2004) A comparison of direct and indirect measures of gene flow in the bat-pollinated tree, Hymenaea courbaril, in the dry-forest life zone of southwestern Puerto Rico. International Journal of Plant Science, 165, 427–436.CrossRefGoogle Scholar
Fuchs, EJ (2007) Population Genetics of the Endangered Tropical Tree, Guaiacum sanctum (Zygophyllaceae). Ph.D. Dissertation, The University of Georgia.Google Scholar
Fuchs, EJ, Hamrick, JL (2010) Mating system and pollen flow between remnant populations of the endangered tropical tree, Guaiacum sanctum (Zygophyllaceae). The importance of isolated trees. Conservation Genetics, in review.
Gerber, S, Chabrier, P, Kremer, A (2003) FAMOZ: A software for parentage analysis using dominant, codominant, and uniparentally inherited markers. Molecular Ecology Notes, 3, 479–481.CrossRefGoogle Scholar
Gonzales, E, Hamrick, JL, Smouse, PE, Trapnell, DW, Peakall, R (2010) The impact of landscape disturbance on spatial genetic structure in the Guanacaste tree, Enterolobium cyclocarpum (Fabaceae). Journal of Heredity, 101, 133–143.CrossRef
Gonzales-Rivas, B, Figabu, M, Gerhardt, K, Castro-Marin, G, Oden, PC (2006) Species composition, diversity, and local uses of tropical dry deciduous and gallery forests in Nicaragua. Biodiversity and Conservation, 15, 1509–1527.CrossRefGoogle Scholar
Hamrick, JL (2001) Breeding patterns of a tropical dry-forest tree species, Enterolobium cyclocarpum, in disturbed and undisturbed habitats. In: Tropical Ecosystems, Structure, Diversity, and Human Welfare (eds. Ganeshaiah, KN, Uma Shaanker, R, Bawa, KS), pp. 291–294. Oxford and IBH Publication Co., New Delhi.Google Scholar
Hamrick, JL, Nason, JD (1996) Consequences of dispersal in plants. In: Population Dynamics and Ecological Space and Time (eds. Rhodes, OE, Chesser, RK, Smith, MH), pp. 203–236. University of Chicago Press, Chicago.Google Scholar
Hanson, T, Brunsfeld, S, Finegan, B, Waits, L (2007) Conventional and genetic measures of seed dispersal for Dipteryx panamensis (Fabaceae) in continuous and fragmented Costa Rican rainforest. Journal of Tropical Ecology, 23, 635–642.CrossRefGoogle Scholar
Hanson, TR, Brunsfeld, SJ, Finegan, B, Waits, LP (2008) Pollen dispersal and genetic structure of the tropical tree, Dipteryx panamensis, in a fragmented Costa Rican landscape. Molecular Ecology, 17, 2060–2073.CrossRefGoogle Scholar
Hardesty, BD, Hubbell, SP, Bermingham, E (2006) Genetic evidence of frequent long-distance recruitment in a vertebrate-dispersed tree. Ecology Letters, 9, 516–525.CrossRefGoogle Scholar
Hedrick, DW (2000) Genetics of Populations. Jones and Bartlett, Sudbury, MA.Google Scholar
Holdridge, LR, Poveda, LJ (1975) Arboles de Costa Rica (Vol. 1). Cantro Cientifico Tropical, San Jose, Costa Rica.Google Scholar
Janzen, DH (1982) Differential seed survival and passage rates in cows and horses, surrogate Pleistocene dispersal agents. Oikos, 38, 150–156.CrossRefGoogle Scholar
Janzen, DH (1986) The future of tropical ecology. Annual Reviews of Ecology and Systematics, 17, 305–324.CrossRefGoogle Scholar
Janzen, DH, Martin, P (1982) Neotropical anachronisms: the fruits the gomphotheres ate. Science, 215, 19–27.CrossRefGoogle ScholarPubMed
Jones, FA, Chen, J, Weng, GJ, Hubbell, SP (2005) A genetic evaluation of seed dispersal in the neotropical tree, Jacaranda copaia (Bignoniaceae). American Naturalist, 166, 543–555.CrossRefGoogle Scholar
Kaufman, SR, Smouse, PE, Alvarez-Buylla, ER (1998) Pollen-mediated gene flow and differential male reproductive success in a tropical pioneer tree, Cecropia obtusifolia Bertal (Moraceae). Heredity, 81, 164–173.CrossRefGoogle Scholar
Linhart, YB (1973) Ecological and behavioral determinants of pollen dispersal in hummingbird-pollinated Heliconia. American Naturalist, 107, 511–523.CrossRefGoogle Scholar
Linhart, YB, Feinsinger, P (1980) Plant-hummingbird interactions: effects of island size and of specialization on pollination. Journal of Ecology, 68, 745–760.CrossRefGoogle Scholar
Lovejoy, T, Bierregaard, R (1990) Central Amazonian forests and the minimum critical size of ecosystems project. In: Four Neotropical Forests (ed. Gentry, A), pp. 60–75. Yale University Press, New Haven, CT.Google Scholar
Nason, JD, Aldrich, PR, Hamrick, JL (1997) Dispersal and the dynamics of genetic structure in fragmented tropical tree populations. In: Tropical Forest Remnants: Ecology, Management, and Conservation in Fragmented Communities (eds. Laurance, WF, Bierregaard, RO), pp. 304–320. University of Chicago Press, Chicago.Google Scholar
Nason, JD, Hamrick, JL (1997) Reproductive and genetic consequences of forest fragmentation: two case studies of neotropical canopy trees. Journal of Heredity, 88, 264–276.CrossRefGoogle Scholar
Nason, JD, Herre, EA, Hamrick, JL (1998) The breeding structure of a tropical keystone plant resource. Nature, 391, 685–687.CrossRefGoogle Scholar
Nei, M, Maruyama, T, Chakrabarty, R (1975) The bottleneck effect and genetic variability in populations. Evolution, 29, 1–10.CrossRefGoogle ScholarPubMed
Opler, PA, Baker, HG, Frankie, GW (1980). Plant reproductive characteristics during secondary succession in neotropical lowland forest ecosystems. Biotropica, 12, 40–46.CrossRefGoogle Scholar
Petit, RJ, Duminil, J, Fineschi, S, Hampe, A, Vendramin, GG (2005) Comparative organization of chloroplasts, mitochondrial and nuclear diversity in plant populations. Molecular Ecology, 14, 689–702.CrossRefGoogle Scholar
Rocha, OJ, Aguilar, G (2001) Reproductive biology of the dry-forest tree, Enterolobium cyclocarpum Jacq. (Guanacaste) in Costa Rica. American Journal of Botany, 88, 1607–1614.CrossRefGoogle Scholar
Roubik, DW (1989) Ecology and Natural History of Tropical Bees. Cambridge University Press, New York.CrossRefGoogle Scholar
Sezen, UU, Chazdon, RL, Holsinger, KE (2007) Multigenerational genetic analysis of tropical secondary regeneration in a canopy palm. Ecology, 88, 3065–3075.CrossRefGoogle Scholar
Sork, VL, Smouse, PE (2006) Genetic analysis of landscape connectivity in tree populations. Landscape Ecology, 21, 821–836.CrossRefGoogle Scholar
Styles, BT (1981). Swietenioidae. In: Flora Neotropica Monograph No. 28: Meliaceae (eds. Pennington, TD, Styles, BT, Taylor, DAH), pp. 359–418. New York Botanical Garden, New York.Google Scholar
Trapnell, DW, Hamrick, JL (2005) Mating patterns and gene flow in the neotropical epiphytic orchid, Laelia rubescens. Molecular Ecology, 14, 75–84.CrossRefGoogle ScholarPubMed
Vekemans, X, Hardy, OJ (2004) New insights from fine-scale spatial genetic structure analyses in plant populations. Molecular Ecology, 13, 921–935.CrossRefGoogle ScholarPubMed
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.CrossRefGoogle ScholarPubMed
White, GM, Boshier, DH, Powell, W (1999) Genetic variation within a fragmented population of Swietenia humilis Zucc. Molecular Ecology, 8, 1899–1909.CrossRefGoogle ScholarPubMed
White, GM, Boshier, DH, Powell, W (2002) Increased pollen flow counteracts fragmentation in a tropical dry-forest: an example from Swietenia humilis Zuccarini. Proceedings of the National Academy of Sciences USA, 99, 2038–2042.CrossRefGoogle Scholar
Wright, S (1951) The genetical structure of populations. Annals of Eugenics, 15, 323–354.CrossRefGoogle ScholarPubMed

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