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Interannual variation in rainfall, drought stress and seedling mortality may mediate monodominance in tropical flooded forests

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Abstract

Flood tolerance is commonly regarded as the main factor explaining low diversity and monodominance in tropical swamps. In this study we examined seedling mortality in relation to seasonality, i.e., flooding versus drought, of the dominant tree species (Prioria copaifera), and three associated species (Pterocarpus officinalis, Carapa guianensis and Pentaclethra macroloba), in seasonally flooded forests (SFF) in Darien, Panama. Seedling mortality differed among species, years and seasons. Prioria seedlings experienced the lowest overall mortality, and after 3 years many more Prioria seedlings remained alive than those of any of the associated species. In general, within species, larger seedlings had greater survival. Seed size, which can vary by close to 2 orders of magnitude in Prioria, had a confounding effect with that of topography. Large-seeded Prioria seedlings experienced 1.5 times greater mortality than small-seeded seedlings, as large-seeded Prioria seedlings were more likely to be located in depressions. This finding suggests that seed size, plant size and topography are important in understanding SFF regeneration. For all species, seedling mortality was consistently greater during the dry season than during flooding. For Prioria, dry season seedling mortality was correlated with drought stress, that is, high mortality during the long El Niño dry season of 1998 and the normal dry season of 2000, but very low dry season mortality during the mild dry season of 1999. Prioria’s ability to dominate in seasonally flooded forest of Central America is partly explained by its low drought-related mortality in comparison to associated species.

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References

  • Baruch Z (1994) Responses to drought and flooding in tropical forage grasses. 1. Biomass allocation, leaf growth and mineral nutrients. Plant Soil 164:87–96

    Article  CAS  Google Scholar 

  • Bebber PD, Brown ND, Speight MR (2004) Dipterocarp seedling population dynamics in Bornean primary lowland forest during the 1997–8 El Niño-Southern Oscillation. J Trop Ecol 20:11–19

    Article  Google Scholar 

  • Bertness MD, Wikler K, Chatkupt T (1992) Flood tolerance and the distribution of Iva frutescens across New England salt marshes. Oecologia 91:171–178

    Article  PubMed  Google Scholar 

  • Bongers F, Poorter L, Van Rompaey RSAR, Parren MPE (1999) Distribution of twelve moist forest canopy tree species in Liberia and Cote d’Ivoire: response curves to a climatic gradient. J Veg Sci 10:371–382

    Article  Google Scholar 

  • Bush MB, Colinvaux P (1994) Tropical forest disturbance: paleoecological records from Darien, Panama. Ecology 75:1761–1768

    Article  Google Scholar 

  • Campbell DG, Daly DC, Prance GT, Maciel UN (1986) Quantitative ecological inventory of terra firme and várzea tropical forest on the Rio Xingú, Brazilian Amazon. Brittonia 38:369–393

    Article  Google Scholar 

  • Clark DB, Clark DA (1992) Life history diversity of canopy and emergent trees in a neotropical rain forest. Ecol Monogr 62:315–344

    Article  Google Scholar 

  • Condit R, Hubbell SP, Foster RB (1995) Mortality rates of 205 Neotropical tree and shrub species and the impact of a severe drought. Ecol Monogr 65:419–439

    Article  Google Scholar 

  • Condit R, Hubbell SP, Foster RB (1996) Changes in tree species abundance in a Neotropical forest: impact of climate change. J Trop Ecol 12:231–256

    Article  Google Scholar 

  • Connell JH (1980) Diversity and the coevolution of competitors, or the ghost of competition past. Oikos 35:131–138

    Article  Google Scholar 

  • Crawford RMM, Braendle R (1996) Oxygen deprivation stress in a changing environment. J Exp Bot 47:145–159

    Article  CAS  Google Scholar 

  • Croat TB (1978) Flora of Barro Colorado Island. Stanford University Press, Palo Alto, Calif.

    Google Scholar 

  • Davis SD, Ewers FW, Sperry JS, Portwood KA, Crocker MC, Adams GC (2002) Shoot dieback during prolonged drought in Ceanothus (Rhamnaceae) Chaparral of California: a possible case of hydraulic failure. Am J Bot 89:820–828

    Article  PubMed  Google Scholar 

  • Delissio LJ, Primack RB (2003) The impact of drought on the population dynamics of canopy-tree seedlings in an aseasonal Malaysian rainforest. J Trop Ecol 19:489–500

    Article  Google Scholar 

  • De Steven D (1994) Tropical tree seedling dynamics: recruitment patterns and their population consequences for three canopy species in Panama. J Trop Ecol 10:369–383

    Article  Google Scholar 

  • Duivenvoorden JF (1996) Patterns of tree species richness in rain forests of the middle Caquetá Area, Colombia, NW Amazonia. Biotropica 28:142–158

    Article  Google Scholar 

  • Estadística Panameña (1987) Situación física; metereología año 1987. Sección 121, clima. Dirección de Estadística y Censo, Contraloría General de la República, Panama

    Google Scholar 

  • Estoque MA, Luque J, Chandek-Monteza M, Garcia J (1985) Effects of El Niño on Panama rainfall. Geofis Int 24:355–381

    Google Scholar 

  • Ferreira LV, Stholgren TJ (1999) Effects of river level fluctuation on plant species richness, diversity, and distribution in a floodplain forest in Central Amazonia. Oecologia 120:582–587

    Article  PubMed  Google Scholar 

  • Golley FB, McGinnis JT, Clements RG, Child GI, Duever MJ (1975) Mineral cycling in a tropical moist forest ecosystem. University of Georgia Press, Athens, Ga.

    Google Scholar 

  • Grauel W, Kursar TA (1999) Species diversity and stand dynamics of Cativo (Prioria copaifera, Griseb.) forests in Darien province, Panama. In: Kleinn C, Kohl M (eds) Proceedings of the IUFRO S4.11 International symposium: Long-Term Observations and Research in Forestry. CATIE, San Jose, pp 69–77

  • Gutierrez F, Dracup JA (2001) An analysis of the feasibility of long-range stream flow forecasting for Colombia using El Niño–Southern Oscillation indicators. J Hydrol 246:181–196

    Article  Google Scholar 

  • Hart TB (1990) Monospecific dominance in tropical rain forest. Trends Ecol Evol 5:6–10

    Article  CAS  PubMed  Google Scholar 

  • Hosmer DW, Lemeshow S (1999) Applied survival analysis: regression modeling of time to event data. Wiley Sons, New York

    Google Scholar 

  • Hubbell SP (1979) Tree dispersion, abundance, and diversity in a tropical dry forest. Science 203:1299–1309

    Article  CAS  PubMed  Google Scholar 

  • Hubbell SP, Foster RB (1986) Biology, chance and the structure of tropical rainforest communities. In: Diamond J, Case TJ (eds) Community ecology. Harper and Row, New York, pp 314–329

    Google Scholar 

  • Huenneke LF, Sharitz RR (1986) Microsite abundance and distribution of woody seedlings in a South Carolina cypress–tupelo swamp. Am Midl Nat 115:328–335

    Article  Google Scholar 

  • Imbert D, Bonheme I, Saur E, Bouchon C (2000) Floristics and structure of the Pterocarpus officinalis swamp forest in Guadeloupe, Lesser Antilles. J Trop Ecol 16:55–68

    Article  Google Scholar 

  • Janzen DH (1974) Tropical blackwater rivers, animals, and mast fruiting by the Dipterocarpaceae. Biotropica 6:69–103

    Article  Google Scholar 

  • Joly CA, Crawford RMM (1982) Variation in tolerance and metabolic responses to flooding in some tropical trees. J Exp Bot 33:799–809

    Article  Google Scholar 

  • Jones RH, Sharitz RR, Dixon PM, Segal DS, Schneider RL (1994) Woody plant regeneration in four floodplain forests. Ecol Monogr 64:345–367

    Article  Google Scholar 

  • Junk WJ (1989) Flood tolerance and tree distribution in central Amazonian floodplains. In: Holm-Nielsen LB, Nielsen IC, Baslev H (eds) Tropical forests. Botanical dynamics, speciation and diversity. Academic Press, San Diego, Calif., pp 45-64

    Google Scholar 

  • Kiladis GN, Diaz HF (1989) Global climatic anomalies associated with extremes in the Southern Oscillation. J Climate 2:1069–1090

    Article  Google Scholar 

  • Kubitzki K, Ziburski A (1994) Seed dispersal in floodplain forest of Amazonia. Biotropica 26:30–43

    Article  Google Scholar 

  • Lopez OR (2001) Seed flotation and post-flooding germination in tropical terra firme and seasonally flooded forest species. Funct Ecol 15:763–771

    Article  Google Scholar 

  • Lopez OR, Kursar TA (2003) Does flood tolerance explain tree species diversity in seasonally flooded habitats? Oecologia 136:193–204

    Article  PubMed  Google Scholar 

  • Lopez OR, Kursar TA, Cochard H, Tyree M (2005) Inter-specific variation in xylem vulnerability to cavitation among tropical trees and shrub species. Tree Physiol 25:1553–1562

    Article  PubMed  Google Scholar 

  • Loreti J, Oesterheld M (1996) Intraspecific variation in the resistance to flooding and drought in populations of Paspalum dilatum from different topographic positions. Oecologia 108:279–284

    Article  CAS  PubMed  Google Scholar 

  • Marques MCM, Joly CA (2000) Estrutura e dinâmica de uma população de Calophyllum brasiliense Camb. em floresta higrofíla do sudeste do Brasil. Rev Bras Bot 23:107–112

    Article  Google Scholar 

  • Parolin P (2000) Seed mass in Amazonian floodplain forests with contrasting nutrient supplies. J Trop Ecol 16:417–428

    Article  Google Scholar 

  • Pitman NCA, Terborgh J, Silman MS, Nuñez P (1999) Tree species distributions in an upper Amazonian forest. Ecology 80:2651–2661

    Article  Google Scholar 

  • Richards PW (1996) The tropical rain forest: an ecological study, 2nd edn. Cambridge University Press, London

    Google Scholar 

  • Ropelewski CF, Halpert MS (1987) Global and regional scale precipitation patterns associated with El Niño/Southern Oscillation. Mon Weather Rev 115:1606–1626

    Article  Google Scholar 

  • Rundel PW, Becker PF (1987) Cambios estacionales en las relaciones hídricas y en la fenología vegetativa de plantas del estrato bajo del bosque tropical de la Isla de Barro Colorado, Panamá. Rev Biol Trop 35:71–84

    Google Scholar 

  • Saverimuttu T, Westoby M (1996) Seedling longevity under deep shade in relation to seed size. J Ecol 84:681–689

    Article  Google Scholar 

  • Schneider RS, Sharitz RR (1988) Hydrochory and regeneration in a bald cypress–water tupelo swamp forests. Ecology 69:1055–1063

    Article  Google Scholar 

  • Schupp EW (1990) Annual variation in seedfall, postdispersal predation, and recruitment of a neotropical tree. Ecology 71:504–515

    Article  Google Scholar 

  • Sheil D, Burslem DFRP, Alder D (1995) The interpretation and misinterpretation of mortality rate measures. J Ecol 83:331–333

    Article  Google Scholar 

  • Shuttleworth WJ, Gash JHC, Lloyd CR, Moore CJ, Roberts J, Marques Filho A de O, Fisch G, Silva Filho V de P, Ribeiro M de NG, Patel SR, de Moraes JC (1984) Eddy correlation measurements of energy partition in amazonian forest. Q J Roy Meteor Soc 110:1143–1162

    Article  Google Scholar 

  • Swanborough P, Westoby M (1996) Seedling relative growth rate and its components in relation to seed size: phylogenetically independent contrasts. Funct Ecol 10:176–184

    Article  Google Scholar 

  • ter Steege H (1994) Flooding and drought tolerance in seeds and seedlings of two Mora species segregated along a soil hydrological gradient in the tropical rain forest of Guyana. Oecologia 100:356–367

    Article  PubMed  Google Scholar 

  • Tobin MF, Lopez OR, Kursar TA (1999) Responses of tropical understory plants to a severe drought: tolerance and avoidance of water stress. Biotropica 31:570–578

    Article  Google Scholar 

  • Walker LR, Zasada JC, Chapin FS III (1989) The role of life history processes in primary succession in an Alaskan floodplain. Ecology 67:1243–1253

    Article  Google Scholar 

  • Walsh RPD (1996) Drought frequency changes in Sabah and adjacent parts of northern Borneo since the late nineteenth century and possible implications for tropical rainforest dynamics. J Trop Ecol 12:385–407

    Article  Google Scholar 

  • Waylen PR, Caviedes CN, Quesada ME (1996) Interannual variability of monthly precipitation in Costa Rica. J Climate 9:2606–2613

    Article  Google Scholar 

  • Weaver PL (1997) Pterocarpus officinalis Jacq. Bloodwood. Department of Agriculture, Forest Service, Southern Forest Experiment Station U.S. SO-ITF-SM-87. New Orleans, La.

    Google Scholar 

  • Williamson BW, Costa F (2000) Dispersal of Amazonian trees: hydrochory in Pentaclethra macroloba. Biotropica 32:548–551

    Google Scholar 

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Acknowledgements

We thank Edmundo Ayarza, Delfin Jaramillo and Bil Grauel for providing invaluable assistance in Darien, to Norberto Badillo for his daily commitment to the rainfall measurement, and to Lissy Coley, Geno Shupp, Fred Adler, Greg Gilbert, Krista Farris-Lopez, Professor Hermann Heilmeier and two anonymous reviewers for valuable discussions and comments on the manuscript. We are grateful for the logistical support of La Palma office of Autoridad Nacional del Ambiente of Panama. This research was supported by a doctoral fellowship (no. 270-98-08) from the Panamanian National Secretariat for Science, Technology and Innovation (SENACYT) and the Institute for Training and Development of Human Resources of Panama (IFARHU) to O.R.L., a NSF Dissertation Improvement Grant (IBN-9902211 to T. A. K. and O. R. L.), and a grant from the International Tropical Timber Organization to the Autoridad Nacional del Ambiente of the Republic of Panama. We (O. R. Lopez and T. A. Kursar), the authors, declare that the research and experiments presented in this publication comply with the current laws of the Republic of Panama.

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Correspondence to Omar R. Lopez.

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Communicated by Hermann Heilmeier.

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Lopez, O.R., Kursar, T.A. Interannual variation in rainfall, drought stress and seedling mortality may mediate monodominance in tropical flooded forests. Oecologia 154, 35–43 (2007). https://doi.org/10.1007/s00442-007-0821-0

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