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Responses of twelve tree species common in Everglades tree islands to simulated hydrologic regimes

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Abstract

Twelve tree species common in Everglades tree islands were subjected to three hydrologic regimes under controlled conditions for 25 weeks and assessed for growth and physiological responses. Treatments representing high, low, and no flood were maintained in pools of water to mimic seasonal variation in water depths at different positions in tree islands. Soil inundation under the high flood treatment resulted in reduced tree growth (height, basal diameter, crown volume) that was more pronounced and occurred earlier in mesic forest species than in swamp forest species. Physiological responses differed less among species, although stomatal conductance was a better predictor of the effects of flood stress on growth than either relative water content or chlorophyll fluorescence (Fv/Fm). Some swamp species appeared to be better adapted to rising water levels than others; Annona glabra, Morella cerifera, and Salix caroliniana responded more positively to flooding, while Magnolia virginiana, Persea borbonia, Chrysobalanus icaco, and Ilex cassine were less flood-tolerant. The highest mortalities and lowest growth were observed in the five upland species: Bursera simaruba, Coccoloba diversifolia, Eugenia axillaris, Sideroxylon foetidissimum, and Simarouba glauca. Of these, Sideroxylon and Simarouba did not survive to the end of the study under the high flood treatment. The moist soil conditions simulated by the low flood treatment resulted in greater growth in all species compared to soil inundation under high flood, except for the most flood-tolerant (Annona, Morella, Salix). The arrangement of species according to their responses to experimental flooding roughly paralleled their spatial distribution in the tree islands. The gradient in species responses demonstrated in this experiment may help guide responsible water management and tree island restoration in the Everglades.

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Literature Cited

  • Alexander, T. R. and A. G. Crook. 1984. Recent vegetational changes in South Florida. p. 199–210. In P. J. Gleason (ed.) Environments of South Florida — Present and Past II, second edition. Miami Geological Society, Coral Gables, FL, USA.

    Google Scholar 

  • Anderson, P. H. and S. R. Pezeshki. 2001. Effects of flood preconditioning on responses of three bottomland tree species to waterlogging. Journal of Plant Physiology 158: 227–233.

    Article  CAS  Google Scholar 

  • Armentano, T. V., D. T. Jones, M. S. Ross, and B. W. Gamble. 2002. Vegetation pattern and process in tree islands of the southern Everglades and adjacent areas. p. 225–282. In F. H. Sklar and A. van der Valk (eds.) Tree Islands of the Everglades. Kluwer Academic Publishers, Dordrecht, The Netherlands.

    Google Scholar 

  • Armstrong, W., R. Brändel, and M. B. Jackson. 1994. Mechanisms of flood tolerance in plants. Acta Botanica Neerlandica 43: 307–358.

    CAS  Google Scholar 

  • Birks, H. J., J. M. Line, S. Juggins, A. C. Stevenson, and C. J. F. ter Braak. 1990. Diatoms and pH reconstruction. Philosophical Transactions of the Royal Society of London (Series B) 327: 263–278.

    Article  Google Scholar 

  • Brandt, L. A., K. M. Portier, and W. M. Kitchens. 2000. Patterns of change in tree islands in Arthur R. Marshall Loxahatchee National Wildlife Refuge from 1950 to 1991. Wetlands 20: 1–14.

    Article  Google Scholar 

  • Broadfoot, W. M. and H. L. Williston. 1973. Flooding effects on southern forests. Journal of Forestry 71: 584–587.

    Google Scholar 

  • Brodribb, T. J., N. M. Holbrook, E. J. Edwards, and M. V. Gutierrez. 2003. Relations between stomatal closure, leaf turgor and xylem vulnerability in eight tropical dry forest trees. Plant, Cell and Environment 26: 443–450.

    Article  Google Scholar 

  • Carlton, G. C. and F. A. Bazzaz. 1998. Regeneration of three sympatric birch species on experimental hurricane blowdown microsites. Ecological Monographs 68: 99–120.

    Article  Google Scholar 

  • Conner, W. H., T. W. Doyle, and D. Mason. 2002. Water depth tolerances of dominant tree island species: what do we know? p. 207–223. In F. H. Sklar and A. van der Valk (eds.) Tree Islands of the Everglades. Kluwer Academic Publishers, Dordrecht, The Netherlands.

    Google Scholar 

  • Craighead, F. C. 1971. The Trees of South Florida, Volume I — The Natural Environments and Their Succession. University of Miami Press, Coral Gables, FL, USA.

    Google Scholar 

  • Craighead, F. C. 1984. Hammocks of South Florida. p. 191–198. In P. J. Gleason (ed.) Environments of South Florida — Present and Past II, second edition. Miami Geological Society, Coral Gables, FL, USA.

    Google Scholar 

  • Davanso, V. M., L. A. de Souza, M. E. Medri, J. A. Pimenta, and E. Bianchini. 2002. Photosynthesis, growth and development of Tabebuia avellanedae Lor. ex Griseb. (Bignoniaceae) in flooded soil. Brazilian Archives of Biology and Technology 45: 375–384.

    Article  Google Scholar 

  • Davis, J. H. 1943. The natural features of Southern Florida, especially the vegetation, and the Everglades. Florida Geological Survey, Tallahassee, FL, USA. Geological Bulletin No. 25.

    Google Scholar 

  • Dickson, R. E., J. F. Hosner, and N. W. Hosley. 1965. The effects of four water regimes upon the growth of four bottomland tree species. Forest Science 11: 299–305.

    Google Scholar 

  • Ewing, K. 1996. Tolerance of four wetland plant species to flooding and sediment deposition. Environmental and Experimental Botany 36: 131–146.

    Article  Google Scholar 

  • Gill, C. J. 1970. The flooding tolerance of woody species — a review. Forestry Abstracts 31: 671–688.

    Google Scholar 

  • Goodall, D. W. 1973. Numerical classification. Handbook of Vegetation Science 5: 107–156.

    Google Scholar 

  • Guerra, R. E. 1997. Impacts of the high water period of 1994–95 on tree islands in Water Conservation Areas. p. 47–58. In T. Armentano (ed.) Ecological Assessment of the 1994–1995 High Water Conditions in the Southern Everglades. South Florida Management and Coordination Working Group, Miami, FL, USA.

    Google Scholar 

  • Gunderson, L. H., J. R. Stenberg, and A. K. Herndon. 1988. Tolerance of five hardwood species to flooding regimes. p. 119–132. In D. A. Wilcox (ed.) Interdisciplinary Approaches to Freshwater Wetlands Research. Michigan State University Press, East Lansing, MI, USA.

    Google Scholar 

  • Gurevitch, J. and S. T. Chester. 1986. Analysis of repeated measures experiments. Ecology 67: 251–255.

    Article  Google Scholar 

  • Harms, W. R., H. T. Schreuder, D. D. Hook, C. L. Brown, and F. W. Shropshire. 1980. The effects of flooding on the swamp forest in lake Ocklawaha, Florida. Ecology 61: 1412–1421.

    Article  Google Scholar 

  • Harper, R. M. 1927. Natural resources of southern Florida. Eighteenth Annual Report. Florida State Geological Survey, Tallahassee, FL, USA.

    Google Scholar 

  • Harshberger, J. W. 1914. The vegetation of south Florida south of 27° 37′ north, exclusive of the Florida Keys. Transactions of the Wagner Free Institute of Science of Philadelphia 7(3): 51–189.

    Google Scholar 

  • Hook, D. D. and C. L. Brown. 1973. Root adaptations and relative flood tolerance of five hardwood species. Forest Science 19: 225–229.

    Google Scholar 

  • Hosner, J. F. 1960. Relative tolerance to complete inundation of fourteen bottomland tree species. Forest Science 6: 246–251.

    Google Scholar 

  • Hosner, J. F. and S. G. Boyce. 1962. Tolerance to water saturated soil of various bottomland hardwoods. Forest Science 8: 180–186.

    Google Scholar 

  • Jackson, M. B. and P. A. Attwood. 1996. Roots of willow (Salix viminalis L.) show marked tolerance to oxygen shortage in flooded soils and in solution culture. Plant and Soil 187: 37–45.

    Article  CAS  Google Scholar 

  • Jones, D. T., T. V. Armentano, S. Snow, and S. Bass. 1997. Evidence for flooding effects on vegetation and wildlife in Everglades National Park, 1994–1995. p. 31–45. In T. V. Armentano (ed.) Ecological Assessment of the 1994–1995 High Water Conditions in the Southern Everglades. South Florida Management and Coordination Working Group, Miami, FL, USA.

    Google Scholar 

  • Keeley, J. E. 1979. Population differentiation along a flood frequency gradient: physiological adaptations to flooding in Nyssa sylvatica. Ecological Monographs 49: 89–108.

    Article  CAS  Google Scholar 

  • Keppel, G. 1973. Design and Analysis: A Researcher’s Handbook. Prentice Hall Inc., Englewood Cliffs, NJ, USA.

    Google Scholar 

  • Kozlowski, T. T. 1982. Water supply and tree growth. II. Flooding. Forestry Abstracts 43: 145–161.

    Google Scholar 

  • Kozlowski, T. T. 1984. Plant responses to flooding of soil. Bioscience 34: 162–167.

    Article  Google Scholar 

  • Kozlowski, T. T., P. J. Kramer, and S. G. Pallardy. 1991. The Physiological Ecology of Woody Plants. Academic Press, London, UK.

    Google Scholar 

  • Kozlowski, T. T. and S. G. Pallardy. 2002. Acclimation and adaptive responses of woody plants to environmental stresses. Botanical Review 68: 270–334.

    Article  Google Scholar 

  • Larson, J. S., M. S. Bedinger, C. F. Bryan, S. Brown, R. I. Huffman, E. L. Miller, D. G. Rhodes, and B. A. Touchet. 1981. Transition from wetlands to uplands in southeastern bottomland hardwood forests. p. 225–269. In J. R. Clark and J. Benfrado (eds.) Wetlands in Bottomland Hardwood Forests. Elsevier Scientific Publishing, New York, NY, USA.

    Google Scholar 

  • Little, E. L. 1978. Atlas of United States Trees, Volume 5: Florida. Miscellaneous Publication No. 1361. U.S. Department of Agriculture, Washington, DC, USA.

    Google Scholar 

  • Liu, F. and H. Stutzel. 2002. Leaf water relations of vegetable amaranth (Amaranthus spp.) in response to soil drying. European Journal of Agronomy 16: 137–150.

    Article  Google Scholar 

  • Lopez, O. R. and T. A. Kursar. 1999. Flood tolerance of four tropical tree species. Tree Physiology 19: 925–932.

    PubMed  Google Scholar 

  • Loveless, C. M. 1959. A study of the vegetation in the Florida Everglades. Ecology 40: 1–9

    Article  Google Scholar 

  • Maceina, M. J., P. W. Bettoli, and D. R. DeVries. 1994. Use of split-plot analysis of variance design for repeated-measures fishery data. Fisheries 19: 14–20.

    Article  Google Scholar 

  • McKevlin, M. R., D. D. Hook, and A. A. Rozelle. 1998. Adaptations of plants to flooding and soil waterlogging. p. 173–203. In M. G. Messina and W. H. Conner (eds.) Southern Forested Wetlands, Ecology and Management. Lewis Publishers, Boca Raton, FL, USA.

    Google Scholar 

  • McKnight, J. S., D. D. Hook, O. G. Langdon, and R. L. Johnson. 1981. Flood tolerance and related characteristics of trees of the bottomland forests of the southern United States. p. 29–69. In J. R. Clark and J. Benfrado (eds.) Wetlands in Bottomland Hardwood Forests. Elsevier Scientific Publishing, New York, NY, USA.

    Google Scholar 

  • McPherson, B. F. 1973. Vegetation in relation to water depth in Conservation Area 3, Florida. U.S. Geological Survey, Tallahassee, FL, USA. Open File Report 73025.

    Google Scholar 

  • Meredith, M. P. and S. V. Stehman. 1991. Repeated measures experiments in forestry: focus on analysis of response curves. Canadian Journal of Forest Research 21: 957–965.

    Article  Google Scholar 

  • Mitsch, W. J. and W. G. Rust. 1984. Tree growth responses to flooding in a bottomland forest in northeastern Illinois. Forest Science 30: 499–510.

    Google Scholar 

  • Ögren, E. and G. Öquist. 1985. Effects of drought on photosynthesis, chlorophyll fluorescence and photoinhibition susceptibility in intact willow leaves. Planta 166: 380–388.

    Article  Google Scholar 

  • Pereira, J. S. and T. T. Kozlowski. 1977. Variations among woody angiosperms in response to flooding. Physiologia Plantarum 41: 184–192.

    Article  Google Scholar 

  • Pezeshki, S. R. and J. L. Chambers. 1986. Variation in floodinduced stomatal photosynthetic responses of three bottomland tree species. Forest Science 32: 914–923.

    Google Scholar 

  • Regehr, D. L., F. A. Bazzaz, and W. R. Boggess. 1975. Photosynthesis, transpiration and leaf conductance of Populus deltoides in relation to flooding and drought. Photosynthetica 9: 52–61.

    Google Scholar 

  • Schmull, M. and F. M. Thomas. 2000. Morphological and physiological reactions of young deciduous trees (Quercus robur L., Q. petraea [Matt.] Lieb., Fagus sylvatica L.) to waterlogging. Plant and Soil 225: 227–242.

    Article  CAS  Google Scholar 

  • Schortemeyer, J. L. 1980. An evaluation of water management practices for optimum wildlife benefits in Conservation Area 3A. Florida Game and Fresh Water Fish Commission, Tallahassee, FL, USA.

    Google Scholar 

  • Sklar, F. H. and A. van der Valk (eds.). 2002a. Tree Islands of the Everglades. Kluwer Academic Publishers, Dordrecht, The Netherlands.

    Google Scholar 

  • Sklar, F. H. and A. van der Valk. 2002b. Tree islands of the Everglades: an overview. p. 1–18. In F. H. Sklar and A. van der Valk (eds.) Tree Islands of the Everglades. Kluwer Academic Publishers, Dordrecht, The Netherlands.

    Google Scholar 

  • Slavik, B. 1974. Methods of Studying Plant Water Relations. Ecological Studies, Volume 9. Springer-Verlag, New York, NY, USA.

    Google Scholar 

  • Smirnoff, N. and R. M. M. Crawford. 1983. Variation in the structure and response to flooding of root aerenchyma in some wetland plants. Annals of Botany 51: 237–249.

    Google Scholar 

  • Sojka, R. E. 1992. Stomatal closure in oxygen-stressed plants. Soil Science 154: 269–280.

    Google Scholar 

  • Teulat, B., P. Monneveux, J. Wery, C. Borries, I. Souyris, A. Charrier, and D. This. 1997. Relationships between relative water content and growth parameters under water stress in barley: a QTL study. New Phytologist 137: 99–107.

    Article  Google Scholar 

  • Tomlinson, P. B. 1980. The Biology of Trees Native to Tropical Florida. Harvard University Printing Office, Allston, MA, USA.

    Google Scholar 

  • USACE. 1999. Central and Southern Florida Project, Comprehensive Review Study, Volume 1, Final Integrated Feasibility Report and Programmatic Environmental Impact Statement. U.S. Army Corps of Engineers, Jacksonville District, Jacksonville, FL, USA.

    Google Scholar 

  • van der Valk, A. and F. H. Sklar. 2002. What we know and should know about tree islands. p. 499–522. In F. H. Sklar and A. van der Valk (eds.) Tree Islands of the Everglades. Kluwer Academic Publishers, Dordrecht, The Netherlands.

    Google Scholar 

  • Vartapetian, B. B. and M. B. Jackson. 1997. Plant adaptations to anaerobic stress. Annals of Botany 79 (Supplement A): 3–20.

    CAS  Google Scholar 

  • Vu, J. C. V. and G. Yelenosky. 1991. Photosynthetic responses of citrus trees to soil flooding. Physiologia Planatarum 81: 7–14.

    Article  CAS  Google Scholar 

  • Wallace, P. M., D. M. Kent, and D. R. Rich. 1996. Responses of wetland tree species to hydrology and soils. Restoration Ecology 4: 33–41.

    Article  Google Scholar 

  • Wetzel, P. R. 2002. Analysis of tree island vegetation communities. p. 357–389. In F. H. Sklar and A. van der Valk (eds.) Tree Islands of the Everglades. Kluwer Academic Publishers, Dordrecht, The Netherlands.

    Google Scholar 

  • Wunderlin, R. P. 1998. Guide to the Vascular Plants of Florida. University Press of Florida, Gainesville, FL, USA.

    Google Scholar 

  • Zotz, G., M. T. Tyree, and S. Patino. 1997. Hydraulic architecture and water relations of a flood-tolerant tropical tree, Annona glabra. Tree Physiology 17: 359–365.

    PubMed  Google Scholar 

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Jones, D.T., Sah, J.P., Ross, M.S. et al. Responses of twelve tree species common in Everglades tree islands to simulated hydrologic regimes. Wetlands 26, 830–844 (2006). https://doi.org/10.1672/0277-5212(2006)26[830:ROTTSC]2.0.CO;2

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  • DOI: https://doi.org/10.1672/0277-5212(2006)26[830:ROTTSC]2.0.CO;2

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