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Reproductive ecology of tropical forest trees in logged and fragmented habitats in Thailand and Costa Rica

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Tropical Forest Canopies: Ecology and Management

Part of the book series: Forestry Sciences ((FOSC,volume 69))

Abstract

Invertebrates mediate several important ecological processes, including pollination and seed predation, and events that affect invertebrate diversity or behaviour can potentially disrupt forest regeneration processes. This study investigates the impact of logging in Thailand and forest fragmentation in Costa Rica on the pollination and seed production of two self-incompatible forest trees. Logging in a dry deciduous dipterocarp forest in Thailand resulted in reduced densities of the common dipterocarp tree Shorea siamensis and variably isolated individual trees. The number of flower visits to S. siamensis by pollinating Trigona bees was not affected by logging disturbance. However, pollinators did spend longer periods of time foraging in the canopies of isolated trees which were more prevalent in logged areas where tree density had been reduced. Consequently, at the logged site few cross-pollinations were effected and fruit set of S. siamensis was considerably lower than at nearby unlogged sites where distances between flowering conspecifics were smaller. Reduced fruit set has long-term implications for the recovery of S. siamensis populations in disturbed areas, and local population genetic structure is likely to be affected as reduced outcrossing rates among trees in disturbed regions results in relatively inbred seed. In Costa Rica forest fragmentation has restricted the once widespread tree Anacardium excelsum to forest patches located in an agriculturally-dominated landscape. As with S. siamensis, the abundance of pollinators, also Trigona bees, in the canopies of A. excelsum was largely unaffected by fragment size. Nevertheless, pollination success and seed production was positively correlated with fragment size. We propose that small bees rarely move between forest fragments and gene exchange through pollination occurs predominantly among trees within fragments and, together with likely low genetic variability in small fragments, that this contributes to the observed reduced fertilisation and seed set of A. excelsum. Thus increased tree isolation tree through selective logging or habitat fragmentation by forest clearance can result in reduced seed set due to changes in the foraging patterns of poorly mobile pollinators. Even if population sizes of the pollinators are maintained following environmental perturbation, this study shows that disturbance may disrupt pollination processes through changes in pollinator foraging behaviour. More attention needs to be focussed on changes in the behaviour of species involved in key ecological interactions following disturbance events in tropical forests.

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References

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

    Google Scholar 

  • Allee, W. C. 1949. Group survival value for Philodina roseola, a rotifer. Ecology 30: 395–397.

    Article  Google Scholar 

  • Bawa, K. S. 1974. Breeding systems of tree species of a lowland tropical community. Evol. 28: 85–92.

    Article  Google Scholar 

  • Bawa, K. S. 1990. Plant-pollinator interactions in tropical rain forests. Ann. Rev. Ecol. Syst. 21: 399–422.

    Google Scholar 

  • Burgman, M. A., Ferson, S. and Akçakaya, H. R. 1992. Risk assessment in conservation biology. Chapman and Hall, London.

    Google Scholar 

  • Epperson, B. K. 1993. Recent advances in correlation studies of spatial patterns of genetic variation. Evol. Biol. 27: 95–155.

    Google Scholar 

  • Fenster, C. B. 1991. Gene flow in Chamaecrista fasciculata (Legu-minosae) I. Gene dispersal. Evolution 45: 398–409.

    Google Scholar 

  • Ghazoul, J. In review. Indirect effects of logging on the reproductive ecology of a butterfly-pollinated tree. J Ecol.

    Google Scholar 

  • Ghazoul, J., Liston, K. A. and Boyle, T. J. B. 1998. Disturbance-induced density-dependent seed set in Shorea siamensis (Dipterocarpaceae), a tropical forest tree. J. Ecol. 86: 462–474.

    Google Scholar 

  • Gigord, L., Lavigne, C. and Shykoff, J. A. 1998. Partial self-incompatibility and inbreeding depression in a native tree species of La Reunion ( Indian Ocean ). Oecologia 117: 342–352.

    Google Scholar 

  • Gigord, L., Picot, F. and Shykoff, J. A. 1999. Effects of habitat fragmentation on Dombeya acutangula (Sterculiaceae), a native tree on La Reunion (Indian Ocean). Biol. Cons. 88: 43–51.

    Google Scholar 

  • Handel, S. N. 1982. Dynamics of gene flow in an experimental population of Cucumis melo (Cucurbitaceae). Am. J. Bot. 69: 1538–1546.

    Google Scholar 

  • Huryn, V. M. B. 1997. Ecological impacts of introduced honey bees. Q. Rev. Biol. 72: 275–297.

    Google Scholar 

  • Jennersten, O. 1988. Pollination in Dianthus deltoides (Caryophyllaceae): effects of habitat fragmentation on visitation and seed set. Cons. Biol. 2: 359–366.

    Google Scholar 

  • Jules, E. S. 1998. Habitat fragmentation and demographic change for a common plant: Trillium in old-growth forest. Ecology 79: 1645–1656.

    Article  Google Scholar 

  • Law, B. S. and Lean, M. 1999. Common blossom bats (Syconycteris australis) as pollinators in fragmented Australian tropical rainforest. Biol. Cons. 91: 201–212.

    Google Scholar 

  • Lugo, A. E. 1995. Management of tropical biodiversity. Ecol. Appl. 5: 956–961.

    Google Scholar 

  • Molano Flores, B., Hendrix, S. D. and Heard, S. B. 1999. The effect of population size on stigma pollen load, fruit set, and seed set in Allium stellatum Ker. (Liliaceae). Int. J. Plant Sci. 160: 753–757.

    Google Scholar 

  • Parra Tabla, V., Vargas, C. F., Magana Rueda, S. and Navarro, J. 2000. Female and male pollination success of Oncidium ascendens Lindey (Orchidaceae) in two contrasting habitat patches: forest vs. agricultural field. Biol. Cons. 94: 335–340.

    Google Scholar 

  • Powell, A. H. and Powell, G. V. N. 1987. Population dynamics of male euglossine bees in Amazonian forest fragments. Biotropica 19: 176–179.

    Article  Google Scholar 

  • Rasmussen, I. R. and BrOdsgaard, B. 1992. Gene flow inferred from seed dispersal and pollinator behaviour compared to DNA analysis of restriction site variation in a patchy population of Lotus corniculatus L. Oecologia 89: 277–283.

    Google Scholar 

  • Rathcke, B. 1983. Competition and facilitation among plants for pollination. Pp. 305–329. In: Real, L. A. (ed), Pollination biology. Academic Press, London.

    Google Scholar 

  • Real, L. A., Otte, J. and Silverfine, E. 1983. On the trade-off between the mean and variance in foraging: an experimental analysis with bumblebees. Ecology 63: 1617–1623.

    Article  Google Scholar 

  • Schaal, B. A. 1980. Measurement of gene flow in Lupinus texensis. Nature 284: 450–451.

    Article  Google Scholar 

  • Smithson, A. and Macnair, M. R. 1997. Density-dependent and frequency-dependent selection by bumblebees Bombus terrestris (L.) ( Hymneoptera: Apidae). Biol. J. Linn. Soc. 60: 401–417.

    Google Scholar 

  • Somanathan, H and Borges, R. M. 2000. Influence of exploitation on population structure, spatial distribution and reproductive success of dioecious species in a fragmented cloud forest in India. Biol. Cons. 94: 243–256.

    Google Scholar 

  • Vinson, S. B., Frankie, G. W. and Barthell, J. 1993. Threats to the diversity of solitary bees in a neotropical dry forest in Central America. Pp. 53–81. In: LaSalle, J. and Gauld, I. D. (eds), Hymenoptera and biodiversity. CAB International, Wallingford.

    Google Scholar 

  • Weidema, I. R., Magnussen, L. S. and Philipp, M. 2000. Gene flow and mode of pollination in a dry-grassland species, Filipendula vulgaris ( Rosaceae ). Heredity 84: 311–320.

    Google Scholar 

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© 2001 Springer Science+Business Media Dordrecht

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Ghazoul, J., McLeish, M. (2001). Reproductive ecology of tropical forest trees in logged and fragmented habitats in Thailand and Costa Rica. In: Linsenmair, K.E., Davis, A.J., Fiala, B., Speight, M.R. (eds) Tropical Forest Canopies: Ecology and Management. Forestry Sciences, vol 69. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-3606-0_27

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  • DOI: https://doi.org/10.1007/978-94-017-3606-0_27

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-90-481-5724-2

  • Online ISBN: 978-94-017-3606-0

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