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Tropical Dry Climates

  • Arturo Sanchez-Azofeifa
  • Margaret E. Kalacska
  • Mauricio Quesada
  • Kathryn E. Stoner
  • Jorge A. Lobo
  • Pablo Arroyo-Mora
Part of the Tasks for Vegetation Science book series (TAVS, volume 39)

Abstract

Based on the Holdridge life zone system (Holdridge 1967) approximately 111, 599, 269 km2 around the world have a climate favorable for dry forest (Leemans 1992, Figure 1). Of that area, 94% is located in the tropics. Tropical dry forests are found between the two parallels of latitude, the Tropics of Cancer and Capricorn (23°27′ N and S) where there are several months of little or no precipitation (Holdridge 1967). In general, three to seven month’s dry season duration has been quoted for seasonally dry forests (Janzen 1983; Murphy and Lugo 1986; Luttge 1997; Piperno and Pearsall 2000). The tropical dry forest ecosystem is one of the most fragile and least protected ecosystems in the world.

Key words

Tropical Remote Sensing Dry Forest Conservation Land cover change 

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References Cited

  1. Aide, T. M., Patterns of leaf development and herbivory in a tropical understory community, Ecology, 74, 455–466, 1993.CrossRefGoogle Scholar
  2. Andren, H., and P. Angelstarn, Elevated predation rates as an edge effect in habitat islands, Ecology, 69, 544–547, 1988.CrossRefGoogle Scholar
  3. Appanah, S., General flowering in the climax rain forest of Southeast Asia, Journal of Tropical Ecology, 1, 225–240, 1985.CrossRefGoogle Scholar
  4. Arroyo-Mora, P., Forest cover assessment, Chorotega Region, Costa Rica, Unpublished M.Sc. Thesis, Department of Earth and Atmospheric Sciences, University of Alberta, Canada, 2002.Google Scholar
  5. Ashton, P. S., T. J. Givnish, and S. Appanah, Staggered flowering in the Dipterocarpaceae: new insights into floral induction and the evolution of mast fruiting in the aseasonal tropics, The American Naturalist, 231, 44–66, 1988.CrossRefGoogle Scholar
  6. Bierregaard, R.O., and T. E. Lovejoy, Effects of forest fragmentation on Amazonian understory bird communities, Acta Amazonica 19, 215–241, 1989.Google Scholar
  7. Borchert, R., Soil and stem water storage determine phenology and distribution of tropical dry forest trees, Ecology, 75, 1437–1449, 1994.CrossRefGoogle Scholar
  8. Bullock, S. H., Plant reproduction in Neotropical dry forests, in Seasonally Tropical Forests, edited by H. A. Mooney, S. H. Bullock, and E. Medina, pp. 277–303, Cambridge University Press, Cambridge, UK, 1995.CrossRefGoogle Scholar
  9. Cascante, A., M. Quesada, J. A. Lobo, and E. J. Fuchs, Effects of dry tropical forest fragmentation on the reproductive success and genetic structure of the tree, Samanea saman, Conserv. Biol., 16, 137–147, 2002.CrossRefGoogle Scholar
  10. Castro-Salazar, R., and G. Arias-Murillo, Costa Rica: Toward the sustainability of its forest resources, Technical Report Fonda Nacional de Financiamiento Foresta (FONAFIFO), San Jose, Costa Rica, 1998.Google Scholar
  11. Chen, J. M., and T. A. Black, Measuring leaf area index of plant canopies with branch architecture, Agricult. Forest Met., 57, 1–12, 1991.CrossRefGoogle Scholar
  12. Chen, J. M., and J. Chilar, Retrieving leaf area index of boreal forests using Landsat TM images, Remote Sens. Environ., 55, 153–162, 1996.CrossRefGoogle Scholar
  13. Chen, J. M., P. M. Rich, S. T. Gower, J. M. Norman, and S. Plummer, Leaf area index of boreal forests: Theory, techniques and measurements, J. Geophys. Res. 102, 429–443, 1997.Google Scholar
  14. Clark, D., Applications of 1m and 4m resolution satellite imagery to studies of tropical forest ecology, management and secondary forest detection, in Tropical Forests: Past, Present, Future, p. 20, The Association of Tropical Biology Annual Meeting, Smithsonian Tropical Research Institute, 2002.Google Scholar
  15. Dirzo, R., and C. A. Dominguez, Plant-herbivore interactions in Mesoamerican tropical dry forests, in Seasonally dry tropical forests, edited by S. H. Bullock, H. A. Mooney, and E. Medina, pp. 277–303, Cambridge University Press, Cambridge, 1995.Google Scholar
  16. Doligez A., and H. Joly, Genetic diversity and spatial structure within a natural stand of a tropical forest tree species, Carapa procera (Meliaceae), in French Guiana, Heredity, 79, 72–82, 1997.Google Scholar
  17. Eby, P., Seasonal movements of grey-headed flying-foxes, Pteropus poliocephalus (Chirpotera: Pteropodidae), from two maternity camps in northern New South Wales, Wildlife Research, 18, 547–559, 1991.CrossRefGoogle Scholar
  18. Ewel, J., Natural systems as models for the design of sustainable systems of land use, Agroforestry Systems, 45, 1–21, 1999.CrossRefGoogle Scholar
  19. Fanjul, L. and V.L. Barradas, Diurnal and seasonal variation in the water relations of some deciduous and evergreen trees of a deciduous dry forest of the western coast of Mexico, J. Appl. Ecol., 24, 289–303, 1987.CrossRefGoogle Scholar
  20. Feinsinger, P., J. A. Wolfe, and L. A. Swarm, Island ecology: reduced hummingbird diversity and the pollination biology of plants on Trinidad and Tobago, West Indies, Ecology, 63, 494–506, 1982.Google Scholar
  21. Fleming, T. H., The short-tailed fruit bat: A study in plant-animal interactions, University of Chicago Press, Chicago, 365 pp., 1988.Google Scholar
  22. Fleming, T. H., R. A. Nuñez, and L. S. L. Sternberg, Seasonal changes in the diets of migrant and non-migrant nectarivorous bats as revealed by carbon stable isotope analysis, Oecologia, 94, 72–75, 1993.CrossRefGoogle Scholar
  23. Flemming, T. H. and V. J. Sosa, Effects of nectarivorous and frugiviorous mammals on reproductive success of plants, J. Mammalogy, 75, 845–851, 1994.CrossRefGoogle Scholar
  24. Frankie, G. W., H. G. Baker, and P. A. Opler, Comparative phenological studies of tress in a tropical lowland wet and dry forest sites of Costa Rica, J. Ecology, 62, 881–913, 1974.CrossRefGoogle Scholar
  25. Frankie, G. W., S. B. Vinson, M. A. Rizzardi, T. L. Griswold, Diversity and abundance of bees visiting a mass flowering tree species in disturbed seasonal dry forest, Costa Rica, Journal of the Kansas Entomological Society, 70, 281–296, 1998.Google Scholar
  26. Fuchs, E. J, J. A. Lobo, and M. Quesada, Effects of forest fragmentation and flowering phenology on the reproductive success and mating patterns on the tropical dry forest tree, Pachira quinata (Bombacaceae), Conserv. Biol., 17, 149–157, 2003.CrossRefGoogle Scholar
  27. Gentry, A. H., Flowering phenology and diversity in tropical Bignoniaceae, Biotropica, 6, 64–68, 1974.CrossRefGoogle Scholar
  28. Gentry, A. H., Diversity of floristic composition of Neotropical dry forests, in Seasonally Tropical Forests, edited by H. A. Mooney, S. H. Bullock, and E. Medina, pp. 146–194, Cambridge University Press, Cambridge, UK, 1995.CrossRefGoogle Scholar
  29. Haber, W. A. and G. W. Frankie, A tropical hawkmoth community: Costa Rican dry forest Sphingidae, Biotropica, 21, 155–172, 1989.CrossRefGoogle Scholar
  30. Haber, W. A., and R. Stevenson, Diversity, migration, and conservation of butterflies in northern Costa Rica, in Biodiversity Conservation in Costa Rica: Learning the Lessons in a Seasonal Dry Forest, edited by G.W. Frankie, A. Mata, and S.B. Vinson, University of California Press, Berkeley, California, 2003.Google Scholar
  31. Hartshorn, G., and B. E. Hammel, Vegetation types and floristic patterns, in La Selva, Ecology and Natural History of a Neotropical Rain Forest, edited by L. McDade, K. S. Bawa, H. A. Hespenheide, and G. Hartshorn, pp. 73–89, University of Chicago Press, Chicago, 1994.Google Scholar
  32. Helversen, O. V., Adaptations of flowers to the pollination by Glossophaginae bats, Animal-plant interactions in tropical environments, edited by W. Barthlott, pp. 41–49, Alexander Koenig Museum, Bonn, Germany, 1993.Google Scholar
  33. Heywood, V. H., G. M. Mace, R. M. May, and S. N. Stuart, Uncertainties in extinction rates, Nature, 368, 105, 1994.CrossRefGoogle Scholar
  34. Holbrook, N. M., J. L. Witbeck, and H. A. Mooney, Drought responses of Neotropical dry forest trees, in Seasonally Tropical Forests, edited by H. A. Mooney, S. H. Bullock, and E. Medina, pp. 243–276, Cambridge University Press, Cambridge, UK, 1995.CrossRefGoogle Scholar
  35. Holdridge L., Life Zone Ecology, Tropical Science Centre, San Jose, Costa Rica, 206 pp., 1967.Google Scholar
  36. Howe, H. F., Implications of seed dispersal by animals for tropical reserve management, Biological Conservation, 30, 261–281, 1984.CrossRefGoogle Scholar
  37. Janzen, D. H., Synchronization of sexual reproduction of trees within dry season in Central America, Ecology, 21, 620–637, 1967.Google Scholar
  38. Janzen, D. H., Herbivores and the number of tree species in tropical forests, American Naturalist, 104, 501–528, 1970.CrossRefGoogle Scholar
  39. Janzen, D. H., Reduction of seed predation on Bauhinia pauletia (Leguminosae) through habitat destruction in a Costa Rican deciduous forest, Brenesia 14/15, 325–336, 1978.Google Scholar
  40. Janzen, D. H., Costa Rica Natural History, University of Chicago Press, Chicago, 816 pp., 1983.Google Scholar
  41. Kalacska, M., G. A. Sánchez-Azofeifa, B. Rivard, P. Arroyo-Mora, R. Hall, J. Zhang, and K. Dutchak, Implications of phenological changes in the extraction of Mesoamerican Tropical Dry Forests through remote sensing: A case study from Costa Rica and Mexico, Proceedings of the International Conference, pp. 84–85, Wageningen University, The Netherlands, 2001.Google Scholar
  42. Leemans, R., Global Holdridge Life Zone Classifications, Digital Raster Data, in Global Ecosystems Database Version 2.0, NOAA National Geophysical Data Center, Boulder, Colorado, 1992.Google Scholar
  43. Lemke, T. O., Foraging ecology of the long-nosed bat Glossophaga soricina with respect to food availability, Ecology, 65, 538–548, 1984.CrossRefGoogle Scholar
  44. Lemke, T. O., Pollen carrying by the nectar-feeding bat Glossophaga soricina in a suburban environment, Biotropica, 17, 107–111, 1985.CrossRefGoogle Scholar
  45. Levey, D. J., T. C. Moermond, and J. S. Denslow, Frugivory: an overview, in La Selva, Ecology and Natural History of a Neotropical Rain Forest, edited by L. McDade, K. S. Bawa, H. A. Hespenheide, and G. Hartshorn, pp. 282–294, University of Chicago Press, Chicago, 1994.Google Scholar
  46. Leopold, A. C., Photoperiodism in plants, Quarterly Review of Biology, 26, 247–263, 1951.PubMedCrossRefGoogle Scholar
  47. Lobo, J. A., M. Quesada, K. E. Stoner, E. J. Fuchs, and Y. Herrerías-Diego, Latitudinal variation of phenological patterns of bombacaceous species in seasonal forests in Costa Rica and Mexico, Amer. J. Botany, (in press), 2003.Google Scholar
  48. Luttge, U., Physiological ecology of tropical plants, Springer-Verlag, Heidelberg, 384 pp., 1997.Google Scholar
  49. Marquis, R. J., Phenological variation in the Neotropical understory shrub Piper arieianum: causes and consequences, Ecology, 69, 1552–1565, 1988.CrossRefGoogle Scholar
  50. Maass, J. M., Conversion of tropical dry forest to pasture and agriculture, in Seasonally Tropical Forests, edited by H. A. Mooney, S. H. Bullock, and E. Medina, pp. 399–422, Cambridge University Press, Cambridge, UK, 1995.CrossRefGoogle Scholar
  51. Medina, E., Diversity of life forms of higher plants in Neotropical dry forests, in Seasonally Tropical Forests, edited by H. A. Mooney, S. H. Bullock, and E. Medina, pp. 221–242, Cambridge University Press, Cambridge, UK, 1995.CrossRefGoogle Scholar
  52. Menaut, J. C., M. Lepage, and L. Abbadie L., Savannas, woodlands and dry forests in Africa, in Seasonally Tropical Forests, edited by H. A. Mooney, S. H. Bullock, and E. Medina, pp. 64–92, Cambridge University Press, Cambridge, UK, 1995.CrossRefGoogle Scholar
  53. Mooney, H.A., S. H. Bullock, and E. Medina, Seasonally Tropical Forests, Cambridge University Press, Cambridge, UK, 450 pp., 1995.Google Scholar
  54. Murphy, P.G. and A. E. Lugo, Ecology of tropical dry forest, Annual Review of Ecology and Systematics, 17, 67–88, 1986.CrossRefGoogle Scholar
  55. Murphy, P.G., and A. E. Lugo, Dry forests of Central America and the Caribbean, in Seasonally Tropical Forests, edited by H. A. Mooney, S. H. Bullock, and E. Medina, pp. 9–34, Cambridge University Press, Cambridge, UK, 1995.CrossRefGoogle Scholar
  56. Murawski, D. A., J. L. Hamrick, S. P. Hubbell, and R. B. Foster, Mating systems of two bombacaceous trees of a Neotropical moist forest. Oecologia, 82, 501–506, 1990.CrossRefGoogle Scholar
  57. Murawski, D. A., and J. L. Hamrick, Mating system and phenology of Ceiba pentandra (Bombacaceae) in Central Panama, J. Heredity, 83, 401–404, 1992.Google Scholar
  58. Murray, K. G., P. Feinsinger, W. H. Busby, Y. B. Linhart, J. H. Beach, P. Kinsman, Evaluation of character displacement among plants in two tropical pollination guilds, Ecology, 68, 1283–1293, 1987.CrossRefGoogle Scholar
  59. Nason, J. D., and J. L. Hamrick, Reproductive and genetic consequences of forest fragmentation: two case studies of neotropical canopy trees, J. Heredity, 88, 264–276, 1997.Google Scholar
  60. Newstrom, L. E., G. W. Frankie, H. G. Baker, and R. K. Colwell, Diversity of long-term flowering patterns, in La Selva, Ecology and Natural History of a Neotropical Rain Forest, edited by L. McDade, K. S. Bawa, H. A. Hespenheide, and G. Hartshorn, pp. 142–160, University of Chicago Press, Chicago, 1994.Google Scholar
  61. Opler, P. A., G. W. Frankie, and H. G. Baker, Rainfall as a factor in the release, timing, and sychronization of anthesis by tropical tress and shrubs, J. Biogeography, 3, 231–236, 1976.CrossRefGoogle Scholar
  62. Piperno, D. R., and D. M. Pearsall, Origins of Agriculture in the Neotropics, Academic Press, New York, 400 pp., 2000.Google Scholar
  63. Price, J. C., and W. C. Bausch, Leaf area index estimation from visible and near-infrared reflectance data, Remote Sens. of Environ., 52, 55–65, 1995.CrossRefGoogle Scholar
  64. Quesada, M., K. E. Stoner, V. Rosas-Guerrero, C. Palacios-Guevara, and J. Lobo, Effects of habitat disruption on the activity of nectarivorous bats (Chiroptera: Phyllostomidae) in a dry tropical forest: implications for the reproductive success of the neotropical tree Ceiba grandiflora, Oecología, 135, 400–406, 2003.PubMedGoogle Scholar
  65. Ratter, J.A., P. W. Richards, G. Argent, and D. R. Gifford, Observations of the vegetation of northeastern Mato Frosso. I. The woody vegetation types of the Xavantina-Cachimbo expedition area, Philosophical Transactions of the Royal Society of London, Series B, 266, 449–492, 1973.CrossRefGoogle Scholar
  66. Reich, P. B. and R. Borchert, Water stress and tree phenology in a tropical dry forest in the tropical dry forest lowlands of Costa Rica, J. Ecology, 72, 61–74, 1984.CrossRefGoogle Scholar
  67. Robertson, C., The philosophy of flower seasons, and the phenological relations of the entomophilous flora and the anthophilous insect fauna, American Naturalist, 29, 97–117, 1895.CrossRefGoogle Scholar
  68. Rolstad, J., Consequences of forest fragmentation for the dynamics of bird populations: Concelptual issues and the evidence, Biological Journal of the Linnean Society, 42, 149–163, 1991.CrossRefGoogle Scholar
  69. Sader, S., and A. T. Joyce, Deforestation rates and trends in Costa Rica, 1940 to 1983, Biotropica, 20(1), 11–19, 1988.CrossRefGoogle Scholar
  70. Sakai, S., K. Momose, T. Yumoto, T. Nagamitsu, H. Nagamasu, A. A. Hamid, and T. Nakasiiizuka, Plant reproductive phenology over four years including an episode of general flowering in a lowland Dipterocarp forest, Sarwak, Malaysia, Amer. J. Botany, 86, 1414–1436, 1999.CrossRefGoogle Scholar
  71. Sanchez-Azofeifa, G.A. and Calvo J., Final report on the extent to Costa Rica forest cover: Year 2002, Costa Rican National Forest Financing Fund, 20 pp., 2002.Google Scholar
  72. Saunders, P. A., Jr., R. J. Hobbs and C. R. Margules, Biological consequences of ecosystem fragmentation: a review, Conservation Biology, 5, 18–32, 1991.CrossRefGoogle Scholar
  73. Stephenson, A. G., The role of extrafloral nectaries of Catalpa speciosa in limiting herbivory and increasing fruit production, Ecology, 63, 663–669, 1982.CrossRefGoogle Scholar
  74. Stiles, G. F., Ecology, flowering phenology, and hummingbird pollination of some Costa Rican Heliconia species, Ecology, 56, 285–301, 1975.CrossRefGoogle Scholar
  75. Stiles, G. F., Coadapted competitors: the flowering seasons of hummingbird-pollinated plants in a tropical forest, Science, 198, 1177–1178, 1977.PubMedCrossRefGoogle Scholar
  76. Stoner, K. E., Seasonal changes in abundance of tropical dry forest frugivorous and nectarivorous bats in northwestern Costa Rica, Canadian Journal of Zoology, 79, 1626–1633, 2001.CrossRefGoogle Scholar
  77. Stoner, K. E., M. Quesada, V. Rosas-Guerrero, and J. A. Lobo, Effects of forest fragmentation on Colima long-nosed bat foraging in tropical dry forest in Jalisco, Mexico, Biotropica, 34, 462–467, 2002.Google Scholar
  78. Stoner, K. E., O. Salazar, K. A., R. C. Fernández,, and M. Quesada Population dynamics, reproduction, and diet of the lesser long-nosed bat (Leptonycteris curasoae) in Jalisco, Mexico: implications for conservation, Biodiversity and Conservation, 12, 357–373, 2003.CrossRefGoogle Scholar
  79. Tallak Nilsen, E., and W. H. Muller, Phenology of the drought-deciduous shrub Lotus scoparius: climatic controls and adaptive significance, Ecological Monographs, 51, 323–341, 1981.CrossRefGoogle Scholar
  80. Trejo, I., and R. Dirzo, Deforestation of seasonally dry tropical forest: a national and local analysis in Mexico, Biological Conservation, 94, 133–142, 2000.CrossRefGoogle Scholar
  81. van der Meer, F., Physical Principals of Optical Remote Sensing, in Spatial Statistics for Remote Sensing (Remote Sensing and Digital Image Processing Vol. 1), edited by A. Stein, F. van der Meer, and B. Gorte, pp. 27–40, Kluwer Academic Publishers, New York, 1999.Google Scholar
  82. van Schaik, C. P., Phenological changes in a Sumatran rain forest, Journal of Tropical Ecology, 2, 327–347, 1986.CrossRefGoogle Scholar
  83. van Schaik, C. P., J. W. Terborgh, and S. J. Wright, The phenology of tropical forests: Adaptive significance and consequences for primary consumers, Annual Review of Ecology and Systematic, 24, 353–377, 1993.CrossRefGoogle Scholar
  84. Walter, H., Ecology of tropical and subtropical vegetation, Oliver and Boyd, Edinburgh, 539 pp., 1971.Google Scholar
  85. Williams-Linera, G., Phenology of deciduous and broad leaf evergreen tree species in a Mexican tropical lower montane forest, Global Ecology and Biogeography Letters, 6, 115–127, 1997.CrossRefGoogle Scholar
  86. Whitmore, T. C., and J. A. Sayer, Deforestation and species extinction in tropical moist forests, in Tropical deforestation and species extinction, edited by T. C. Whitmore and J. A. Sayer, pp. 1–14, Chapman and Hall, London, 1992.Google Scholar
  87. Wright, S. J., Seasonal drought and the phenology of shrubs in a tropical moist forest, Ecology, 72, 1643–1657, 1991.CrossRefGoogle Scholar
  88. Wright, S. J., and P. vn Schaik, Light and the phenology of tropical trees, The American Naturalist, 143, 192–199, 1994.CrossRefGoogle Scholar
  89. Wright, S. J., and F. H. Cornejo, Seasonal drought and leaf fall in a tropical forest, Ecology 71, 1165–1175, 1990.CrossRefGoogle Scholar
  90. Zimmerman, J. K., D. W. Roubik, J. D. Ackerman, Asynchronous phenology of a neotropical orchid and its euglossine bee pollinators, Ecology, 70, 1192–1195, 1989.CrossRefGoogle Scholar

Copyright information

© Kluwer Academic Publishers 2003

Authors and Affiliations

  • Arturo Sanchez-Azofeifa
    • 1
  • Margaret E. Kalacska
    • 1
  • Mauricio Quesada
    • 2
  • Kathryn E. Stoner
    • 2
  • Jorge A. Lobo
    • 3
  • Pablo Arroyo-Mora
    • 4
  1. 1.Earth and Atmospheric Sciences DepartmentUniversity of AlbertaEdmontonCanada
  2. 2.Centro de Investigaciones en EcosistemasUniversidad Nacional Autónoma de MéxicoMoreliaMéxico
  3. 3.Biology DepartmentUniversidad de Costa RicaSan JoseCosta Rica
  4. 4.Department of Ecology and Evolutionary BiologyUniversity of ConnecticutStorrsUSA

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