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16 - Rainforest mineral nutrition: the ‘black box’ and a glimpse inside it

from Part II - Hydrological processes in undisturbed forests

Published online by Cambridge University Press:  12 January 2010

J. Proctor
Affiliation:
Department of Biological Sciences, University of Stirling, Stirling, FK9 4LA, UK
M. Bonell
Affiliation:
UNESCO, Paris
L. A. Bruijnzeel
Affiliation:
Vrije Universiteit, Amsterdam
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Summary

INTRODUCTION

This chapter deals mainly with undisturbed tropical rainforests and its aims are threefold:

  • to summarise the current knowledge of selected topics in rainforest mineral nutrition;

  • to emphasise the links between hydrology, pedogenesis and rainforest mineral nutrition; and

  • to identify the most important gaps in knowledge and to suggest the most promising lines of research.

The rainforest nutrient cycle

Nutrients enter the ecosystem with rain, deposition of dust and aerosols, by fixation by microorganisms (in the case of N) above and below ground, and (except for N) by weathering of the substratum (Figure 16.1). The major above-ground pool of nutrients is formed in the tree boles and large branches. There is a flow of nutrients from these and the many other components of the above-ground pool of nutrients to the forest floor in small and large litterfall and in throughfall and stemflow of rainwater, enriched by nutrients from leaves and bark. The nutrients in dead organic matter are released gradually by decomposition, mediated by soil animals and microorganisms. Decomposition can involve immobilisation of nutrients as well as their release. In extreme cases the immobilisation may involve a conversion of the litter to stable organic matter which holds nutrients indefinitely. Such occurs in those forest types that have very wet or acid conditions (such as heath forests, peat swamp forests and upper montane cloud forests) which are described by Whitmore (1984).

Type
Chapter
Information
Forests, Water and People in the Humid Tropics
Past, Present and Future Hydrological Research for Integrated Land and Water Management
, pp. 422 - 446
Publisher: Cambridge University Press
Print publication year: 2005

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References

Adámoli, J., Sennhauser, E., Acero, J. M. and Rescia, A. (1991). Stress and disturbance: vegetation dynamics in the dry Chaco region of Argentina. Savanna Ecology and Management. Australian Perspectives and Intercontinental Comparisons, ed. P. Werner, pp. 147–156. Oxford: Blackwell Scientific Publications
Alexander, I. J., Norani, A. and Lee, S. S. (1992). The role of mycorrhizas in the regeneration of some Malaysian forest trees. Philosophical Transactions of the Royal Society of London B, 335, 379–388CrossRefGoogle Scholar
Alexandre, A., Meunier, J.-D., Colin, F. and Koud, J. M. (1997). Plant impact on the biogeochemical cycle of silicon and related weathering processes. Geochimica et Cosmochimica Acta, 61, 677–682CrossRefGoogle Scholar
,Anonymous (1972). Regenwasseranalysen aus Zentralamazonien, ausgefuhrt in Manaus, Amazonia, Brasilien, von Dr. Harald Ungemach. Amazoniana, 3, 186–198Google Scholar
Antibus, R. K.. (1997). Root surface phosphatase activities and uptake of 32P-labelled inositol phosphate in field collected gray birch and red maple roots. Mycorrhiza, 7, 39–46CrossRefGoogle Scholar
Asbury, A. E., McDowell, R., Trinidad-Pizarro, R. and Berrios, S. (1994). Solute deposition from cloud water to the canopy of a Puerto Rican montane forest. Atmospheric Environment, 28, 1773–1780CrossRefGoogle Scholar
Ashton, P. S. (1976). Mixed dipterocarp forest and its variation with habitat in the Malayan lowlands: a re-evaluation at Pasoh. Malaysian Forester 39, 56–72Google Scholar
Austin, M. P., and Greig-Smith, P. (1968). The application of quantitative methods to vegetation survey. II. Some methodological problems of data from rainforest. Journal of Ecology, 56, 827–844CrossRefGoogle Scholar
Bach, L. B., Wierenga, P. J., and Ward, T. J. (1986). Estimation of the Philip infiltration parameters from rainfall simulation data. Soil Science Society of America Journal, 50, 1319–1323CrossRefGoogle Scholar
Baillie, I. C. (1989). Soil characteristics and classification in relation to the mineral nutrition of tropical wooded ecosystems. In Mineral Nutrients in Tropical Forest Ecosystems ed. J. Proctor, pp., 15–26. Oxford: Blackwell Scientific Publications
Baillie, I. C. and Ashton, P. S. (1983). Some aspects of the nutrient cycle in mixed dipterocarp forests in Sarawak. In Tropical Rain Forest: Ecology and Management, ed. S. L. Sutton, T. C. Whitmore, and A. C. Chadwick, pp. 347–356. Oxford: Blackwell Scientific Publications
Baillie, I. C. (1996). Soils of the humid tropics. In The Tropical Rain Forest (ed. P. W. Richards), pp. 256–286. Cambridge: Cambridge University Press
Barcelo, J., Guevara, P., and Poschenrieder, C. (1993). Silicon amelioration of aluminium toxicity in teosinte (Zea mays L. ssp. mexicana. Plant and Soil, 154, 249–255CrossRefGoogle Scholar
Boersma, M., van Schaik, C. P. and Hogeweg, P. (1991). Nutrient gradients and spatial structure in tropical forests: a model study. Ecological Modelling, 55, 219–240CrossRef
Blum, J. D., Erel, Y. and Brown, K. (1994). 87Sr/86Sr ratios of Sierra Nevada stream waters: implications for relative mineral weathering rates. Geochimica and Cosmochimica Acta, 58, 5019–5025Google Scholar
Bolan, N. S., Naidu, R., Mahimairaja, S., and Baskaran, S. (1994). Influence of low-molecular weight organic acids on the solubilization of phosphates. Biology and Fertility of Soils, 18, 311–319CrossRefGoogle Scholar
Brandes, J. A., McClain, M. E., and Pimentel, T. P. (1996). 15N evidence for the origin and cycling of inorganic nitrogen in a small Amazonian catchment. Biogeochemistry, 34, 45–56CrossRefGoogle Scholar
Brasell, H. M., and Gilmour, D. A. (1980). The cation composition of precipitation at four sites in far north Queensland. Australian Journal of Ecology, 5, 397–405CrossRefGoogle Scholar
Brinkmann, W. L. F. (1983). Nutrient balance of a central Amazonian rainforest: comparison of natural and man-managed ecosystems. Hydrology of Humid Tropical Regions with Particular Reference to the Hydrological Effects of Agriculture and Forestry Practice, IAHS Publication No. 140, pp. 153–163
Brinkmann, W. L. F. (1985). Studies on hydrogeochemistry of a tropical lowland forest system. Geojournal, 11, 89–101CrossRefGoogle Scholar
Brouwer (1996). Nutrient Cycling in Pristine and Logged Tropical Rain Forest. A Study in Guyana. The Netherlands: University of Utrecht
Bruijnzeel, L. A. (1989). Nutrient content of bulk precipitation in south-central Java, Indonesia. Journal of Tropical Ecology, 5, 187–202CrossRefGoogle Scholar
Bruijnzeel, L. A. (1989b). Nutrient cycling in moist tropical forests: the hydrological framework. In Mineral Nutrients in Tropical Forest and Savanna Ecosystems, ed. J. Proctor, pp. 383–415. Oxford: Blackwell Scientific Publications
Bruijnzeel, L. A. (1991). Nutrient input-output budgets of tropical forest ecosystems: a review. Journal of Tropical Ecology, 7: 1–23CrossRefGoogle Scholar
Bruijnzeel, L. A. (1998). Soil chemical changes after tropical forest disturbance and conversion: the hydrological perspective. In Soils of Tropical Forest Ecosystems, ed. A. Schulte and D. Ruhiyat, pp. 45–61. Berlin: SpringerCrossRef
Burgess, S. S. O., Dubinsky, E. and Dawson, T. E. (2001). The role of fog in the ecology and water relations of coast redwood Sequoia sempervirens. In R. S. Schemenauer and H. A. Puxbaum (Eds). Proceedings of the 2nd International Conference on Fog and Fog Collection, 15–20 July 2001, St. John's, Canada, pp. 121–124
Burghouts, T. B. A., Stralen, N. M. and Bruijnzeel, L. A. (1998). Spatial heterogeneity of element and litter turnover in a Bornean rainforest. Journal of Tropical Ecology, 14, 477–506CrossRefGoogle Scholar
Burnham, C. P. (1989). Pedological processes and nutrient supply from parent material in tropical soils. In Mineral Nutrients in Tropical Forest and Savanna Ecosystems, ed. J. Proctor, pp. 27–41. Oxford: Blackwell Scientific Publications
Burslem, D. F. R. P., Grubb, P. J., and Turner, I. M. (1995). Responses to nutrient addition among shade-tolerant tree seedlings of lowland tropical forest in Singapore. Journal of Ecology 83, 113–122CrossRefGoogle Scholar
Burslem, D. F. R. P., Grubb, P. J., and Turner, I. M. (1996). Responses to simulated drought and elevated nutrient supply among shade-tolerant tree seedlings of lowland tropical forest in Singapore. Biotropica, 28, 636–648CrossRefGoogle Scholar
Burslem, D. F. R. P., Turner, I. M., and Grubb, P. J. (1994). Mineral nutrient status of coastal hill dipterocarp forest and Adinandra belukar in Singapore: bioassays of nutrient limitation. Journal of Tropical Ecology, 10, 579–599CrossRefGoogle Scholar
Cavelier, J., Jaramillo, M., Solis, D., and Léon., D. (1997). Water balance and nutrient inputs in bulk precipitation in tropical montane cloud forest In Panama. Journal of Hydrology, 193, 83–96CrossRefGoogle Scholar
Chalot, M. and Brun, A. (1998). Physiology of organic nitrogen acquisition by ectomycorrhizal fungi and ectomycorrhizas. FEMS Microbiological Reviews, 2, 21–44CrossRefGoogle Scholar
Chandler, G. (1985). Mineralization and nitrification in three Malaysian forest soils. Soil Biology and Biochemistry, 17, 347–353CrossRefGoogle Scholar
Chapin, F. S. (1980). The mineral nutrition of wild plants. Annual Review of Ecology and Systematics, 11, 233–260CrossRefGoogle Scholar
Chestnut, T. J. and McDowell, W. H. (2000). C and N dynamics in the riparian and hyporheic zones of a tropical stream, Luquillo Mountains, Puerto Rico. Journal of the North American Benthological Society, 19, 199–214CrossRefGoogle Scholar
Clark, K. L., Nadkarni, N. M., Schaeffer, D. and Gholz, H. L. (1998). Atmospheric deposition and net retention of ions by the canopy in a tropical montane forest, Monteverde, Costa Rica. Journal of Tropical Ecology, 14, 27–45CrossRefGoogle Scholar
Clarkson, (1966). Aluminium tolerance in species within the genus Agrostis. Journal of Ecology, 53, 427–435CrossRefGoogle Scholar
Coleman, D. C., Reid, C. P. P. and Cole, C. V. (1983). Biological strategies of nutrient cycling in soil systems. Advances in Ecological Research, 13, 1–55CrossRefGoogle Scholar
Coomes, D. A., (1995). The Effects of Root Competition on Saplings and Seedlings in Amazonian Caatinga Forest in Southern Venezuela. Ph. D. thesis, University of Cambridge, U.K.
Courchesne, F., Savoie, S., and Dufresne, A. (1995). Effects of air-drying on the measurement of soil pH in acidic forest soils of Quebec, Canada. Soil Science, 160, 56–67CrossRefGoogle Scholar
Crews, T. E., Kitayama, K., Fownes, J. H., Riley, R. H., Herbert, D. A., Mueller-Dombois, D., and Vitousek, P. M. (1995). Changes in soil phosphorus and ecosystem dynamics across a long chronosequence in Hawaii. Ecology, 76, 1407–1424CrossRefGoogle Scholar
Crocker, R. L. and Major, J. (1955). Soil development in relation to vegetation and surface age, Glacier Bay, Alaska. Journal of Ecology, 43, 427–448CrossRefGoogle Scholar
Cromer, R. N., Cameron, D. N., Rance, S. J., Ryan, P., and Brown, M. (1993a). Response to nutrients in Eucalyptus grandis. 1. Biomass accumulation. Forest Ecology and Management, 62, 211–230CrossRefGoogle Scholar
Cromer, R. N., Cameron, D. N., Rance, S. J., Ryan, P., and Brown, M. (1993b). Response to nutrients in Eucalyptus grandis. 2. Nitrogen accumulation. Forest Ecology and Management, 62, 231–243CrossRefGoogle Scholar
Cromer, R. N., Kriedemann, P. E., Sands, P. J., and Stewart, L. G. (1993c). Leaf growth and photosynthetic response to nitrogen and phosphorus in seedling trees of Gmelina arborea. Australian Journal of Plant Physiology, 20, 83–98CrossRefGoogle Scholar
Cuevas, E. and Medina, E. (1988). Nutrient dynamics within Amazonian forest. II Fine root growth, nutrient availability and leaf litter decomposition. Oecologia, 76, 222–235CrossRefGoogle ScholarPubMed
Dalling, J. W., and Tanner, E. V. J. (1995). An experimental study of regeneration on landslides in montane rainforest in Jamaica. Journal of Ecology, 83, 55–64CrossRefGoogle Scholar
Denslow, J. S. (1980). Patterns of plant species diversity during succession under different disturbance regimes. Oecologia, 46, 18–21CrossRefGoogle ScholarPubMed
Denslow, J. S., Vitousek, P. M., and Schultz, J. C. (1987). Bioassays of nutrient limitation in a tropical rainforest soil. Oecologia, 74, 370–376CrossRefGoogle Scholar
Rham, P. (1970). L'azote dans quelques fôrets, savanes et terrains de culture d'Afrique tropicale humide. Veröffentlichen des Geobotanischen Institutes der Eidgenössische Technische Hochschule, Stiftung Rübel in Zurich, 45Google Scholar
Drever, J. I. (1994). The effect of land plants on weathering rates of silicate minerals. Geochimica and Cosmochimica Acta, 58, 2325–2332CrossRefGoogle Scholar
Drew, M. C. and Nye, P. H. (1969). The supply of nutrient ions by diffusion to plant roots in the soil. II. The effect of root hairs on the uptake of potassium by roots of rye-grass (Lolium multiflorum). Plant and Soil, 31, 407–424CrossRefGoogle Scholar
Epstein, E. (1994). The anomaly of silicon in plant biology. Proceedings of the National Academy of Sciences, 91, 11–17CrossRefGoogle ScholarPubMed
Evans, J. R. (1989). Photosynthesis and nitrogen relationships in leaves of C3 plants. Oecologia, 78, 9–19CrossRefGoogle ScholarPubMed
Fetcher, N., Haines, B. L., Cordero, R. A., Lodge, D. J., Walker, L. R., Fernandez, D. S., and Lawrence, W. T. (1996). Responses of tropical plants to nutrients and light on a landslide in Puerto Rico. Journal of Ecology, 84, 331–341CrossRefGoogle Scholar
Fitter, A. H. (1986). Effect of benomyl on leaf phosphorus concentration in alpine grasslands: a test of mycorrhizal benefit. New Phytologist, 103, 767–776CrossRefGoogle Scholar
Fitter, A. H. and Hay, R. K. M. (2002). Environmental Physiology of Plants. 3rd edition. London: Academic Press
Forti, M. C. and Neal, C. (1992). Hydrochemical cycles in tropical rainforests: an overview with emphasis on Central Amazonia. Journal of Hydrology, 134, 103–115CrossRefGoogle Scholar
Franco, W. and Dezzeo, N. (1994). Soils and soil water regime in the terra firme-caatinga forest complex near San Carlos de Rio Negro, State of Amazonia, Venezuela. Interciencia, 19, 305–316Google Scholar
Franken, W. and Leopoldo, P. R. (1984). Hydrology of catchment areas of Central-Amazonian forest streams. In The Amazon. Limnology and Landscape Ecology of a Mighty Tropical River and its Basin, ed. H. Sioli, pp. 501–509. Dordrecht: W. JunkCrossRef
Freeden, A. L., Griffin, K, and Field, C. B. (1991). Effects of light quantity and quality and soil nitrogen status on nitrate reductase activity in rain forest species of the genus Piper. Oecologia, 85, 441–446CrossRefGoogle Scholar
Gautam-Basak, M., and Proctor, J. (1983). Micronutrients, silicon and ash in leaf litterfall from forests in Gunung Mulu National Park, Sarawak. Malaysian Forester 46, 224–232Google Scholar
Gilman, G. P., Sinclair, D. F., Knowlton, R., and Keys, M. G., 1985. The effect on some soil chemical properties of the selective logging of a north Queensland rainforest. Forest Ecology and Management, 12, 195–214CrossRefGoogle Scholar
Godbold, D. L., Fritz, E., and Hutterman, A. (1988). Aluminium toxicity and forest decline. Proceedings of the National Academy of Sciences U.S.A., 85, 3888–3892CrossRefGoogle ScholarPubMed
Green, J. J. (1992). Fine Root Dynamics in a Bornean Rain Forest. Unpublished Ph. D. thesis, University of Stirling, U.K.
Grimaldi, C., Luizão, R. C. and Chauvel, A. (1992). Hydric and biogeochemical pulses in the functioning of soils in Amazonian forest ecosystems. In Second International Symposium on Environmental Studies of Tropical Rainforests- Forest 92 Proceedings Volume, ed. Anon., pp. 170–171. Rio de Janeiro: Brazilian Society for the Environment
Grime, J. P. (1977). Evidence for the existence of three primary strategies in plants and its relevance to ecological and evolutionary theory. American Naturalist, 111, 1169–1194CrossRefGoogle Scholar
Gunatilleke, C. V. S., Gunatilleke, I. A. U. N., Perera, G. A. D., Burslem, D. F. R. P., Ashton, P. M. S., and Ashton, P. S. (1997). Responses to nutrient addition among seedlings of eight closely related species of Shorea in Sri Lanka. Journal of Ecology, 85, 301–311CrossRefGoogle Scholar
Hafkenscheid, L. L. R. (2000). Hydrology and Biogeochemistry of Tropical Montane Rain Forests of Contrasting Stature in the Blue Mountains, Jamaica. Amsterdam: Free University
Handley, L. and Scrimgeour, C. M. (1997). Terrestrial plant ecology and δ15N natural abundance: thepresent limits to interpretation for uncultivated systems with original data from a Scottish old field. Advances in Ecological Research, 27, 133–212CrossRefGoogle Scholar
Harley, J. and Smith, S. E. (1983). Mycorrhizal Symbiosis. London: Academic Press
Heaney, A. and Proctor, J. (1989). Chemical elements in litter in forests on Volcán Barva, Costa Rica. In Mineral Nutrients in Tropical Forest and Savanna Ecosystems, ed. J. Proctor, pp. 255–271. Oxford: Blackwell Scientific Publications
Hedley, M. J., Stewart, J. W. B., and Chauhan, B. S. (1982). Changes in inorganic and organic soil phosphorus fractions induced by cultivation practices and by laboratory incubations. Soil Science Society of America Journal, 46, 970–976CrossRefGoogle Scholar
Hendry, C. D., Berish, C. W. and Edgerton, E. S. (1984). Precipitation chemistry at Turrialba, Costa Rica. Water Resources Research, 20, 1677–1684CrossRefGoogle Scholar
Herrera, R., Merida, T., Stark, N.et al. (1978). Direct phosphorus transfer from leaf litter to roots. Naturwissenschaften, 65, 208–209CrossRefGoogle Scholar
Hobbs, R. J. (2001). From our southern correspondent. Bulletin of the British Ecological Society, 32, 32–33Google Scholar
Hofstede, R. M., Wolf, J. H. D., and Benzing, D. H. (1993) Epiphytic biomass and nutrient status of a Colombian upper montane rain forest. Selbyana, 14, 37–45Google Scholar
Huttel, C. (1975). Root distribution and biomass in three Ivory Coast rainforest plots. In Tropical Ecological Systems ed. F. B. Golley and E. Medina, pp. 123–130. Berlin: SpringerCrossRef
Jacobs, M. (1988). The Tropical Rain Forest. A First Encounter. London: SpringerCrossRef
Jongmans, A. G., Breemen, N. V., Lundstrom, U., Finlay, R. D., Hees, P. A. W., Giesler, R., Melkereud, P.-A., Olsson, M., Srinavasan, M., and Unestam, T. (1997). Rock-eating fungi: a true case of mineral plant nutrition?Nature, 389, 682–683CrossRefGoogle Scholar
Jones, J. M. and , Richards B. N. (1977). Effect of reforestation on turnover of N-15 labelled ammonium plus nitrate in relation to changes in soil microflora. Soil Biology and Biochemistry, 9, 383–392CrossRefGoogle Scholar
Jordan, C. F. and Herrera, R. (1981). Tropical rainforests: are nutrients really critical?American Naturalist, 117, 167–180CrossRefGoogle Scholar
Jordan, C. F., Kline, J. R., and Saszcer, D. S. (1972). Relative stability of mineral cycles in forest ecosystems. American Naturalist, 106, 237–254CrossRefGoogle Scholar
Kelly, E. F., Chadwick, O. A. and Hilsinki, T. E. (1998). The effect of plants on mineral weathering. Biogeochemistry, 42, 21–53CrossRefGoogle Scholar
Khiewtam, R. S. and Ramakrishnan, P. S. (1993). Litter and fine root dynamics of a relict sacred grove forest at Cherrapunji in north-eastern India. Forest Ecology and Management, 60, 327–344CrossRefGoogle Scholar
Kidd, P. S. and Proctor, J. (2000a). The growth response of ecotypes of Holcus lanatus from different soil types in northwestern Europe to phenolic acids. Plant Biology 2, 335–343CrossRefGoogle Scholar
Kidd, P. S. and Proctor, J. (2000b). Effects of aluminium on the growth and mineral composition of Betula pendula Roth. Journal of Experimental Botany, 51, 1057–1066CrossRefGoogle Scholar
Kidd, P. S. and Proctor, J. (2001a). Why plants grow poorly on very acid soils: are ecologists missing the obvious?Journal of Experimental Botany, 52, 791–799CrossRefGoogle Scholar
Kidd, P. S. and Proctor, J. (2001b). The growth response of ecotypes of Holcus lanatus L. from different soil types in northwestern Europe to aluminium and silicon. Fresenius Environmental Bulletin, 10, 590–594Google Scholar
Killingbeck, K. T. (1996). Nutrients in senesced leaves: keys to the search for potential resorption and resorption proficiency. Ecology, 77, 1716–1727CrossRefGoogle Scholar
King, H. B. and Yang, B. Y. (1984). Precipitation and stream water chemistry in Pi-Lu-Chi watersheds. January, 1981—December, 1982. Bulletin of the Taiwan Forestry Research Institute, Taipei. no. 427. (In Chinese with English summary)
Kinraide, T. B. (1993). Aluminium enhancement of plant growth in acid rooting media. A case of reciprocal alleviation of toxicity by two toxic cations. Physiologia Plantarum, 88, 619–625CrossRefGoogle ScholarPubMed
Klinge, H. (1973). Root mass estimation in lowland tropical rainforests of central Amazonia, Brazil. I. Fine root masses of a pale yellow latosol and a giant humus podzol. Tropical Ecology, 14, 29–38Google Scholar
Klinge, H. (1976). Bilanzierung von Hauptnahrstoffen in okosystem tropischer Regenwald (Manaus)-vorlaufige Daten. Biogeographica, 7, 59–76Google Scholar
Klinge, R., Schmidt, J. and Fölster, H. (2001). Simulation of water drainage of a rainforest and forest conversion plots using a soil water model, Journal of Hydrology, 246, 82–95CrossRefGoogle Scholar
Kuiters, A. T. (1990). Role of phenolic substances from decomposing forest litter in plant-soil interactions. Acta Botanica Neerlandica, 39, 329–348CrossRefGoogle Scholar
Lamb, D. (1980). Soil nitrogen mineralization in a secondary forest succession. Oecologia, 47, 257–263CrossRefGoogle Scholar
Lambers, H., Chapin, F. S., and Pons, T. L. (1998). Plant Physiolgical Ecology. New York: Springer
Landeweert, R., Hoffland, E., Finlay, R. D., Kuyper, T. W., and Breemen, N. (2001). Linking plants to rocks: ectomycorrhizal fungi mobilize nutrients from minerals. Trends in Ecology and Evolution, 16, 248–254CrossRefGoogle ScholarPubMed
Laverman, A. M., Zoomer, H. R., Engelbrecht, D., Berg, M. P., Straalen, N. M., Verseveld, H. W., and Verhoef, H. A. (2000a). Soil layer specific variability in net nitrification and denitrification in an acid coniferous forest. Biology and Fertility of Soils, 32, 427–434CrossRefGoogle Scholar
Laverman, A. M., Zoomer, H. R., Verseveld, H. W., and Verhoef, H. A. (2000b). Temporal and spatial variations of nitrogen transformations in an acid coniferous forest. Soil Biology and Biochemistry, 32, 1661–1670CrossRefGoogle Scholar
Laverman, A. M., Zoomer, H. R., and Verhoef, H. A. (2001). The effect of oxygen, pH and organic carbon on soil-layer specific denitrifying capacity in acid coniferous forest. Soil Biology and Biochemistry, 33, 683–687CrossRefGoogle Scholar
Lawson, G. W., Armstrong-Mensah, K. O., and Hall, J. B. (1970). A catena in tropical moist semi-deciduous forest near Kade, Ghana. Journal of Ecology, 58, 371–398CrossRefGoogle Scholar
Lee, S. S. and Alexander, I. J. (1994). The response of seedlings of two dipterocarp species to nutrient additions and ectomycorrhizal infection. Plant and Soil, 163, 299–306Google Scholar
Lesack, L. F. W. (1993). Export of nutrients and major ionic solutes from a rainforest catchment in the Central Amazon basin. Water Resources Research, 29, 743–758CrossRefGoogle Scholar
Lloyd, P. S. and Pigott, C. D. (1967). The influence of soil conditions on the course of succession in southern England. Journal of Ecology, 55, 137–146CrossRefGoogle Scholar
Lucas, Y., Nahon, D., Cornu, S., and Eyrolle, F. (1996). Genèse et fonctionnement des sols en milieu équatorial. Comptes Rendues de l' Académie des Sciences, 322, lla, 1–16Google Scholar
Luizão, F. J. (1996). Ecological studies in Contrasting Forest Types in Central Amazonia. Unpublished Ph. D. thesis, University of Stirling, U.K.
Luizão, F. J., Proctor, J., Thompson, J., Luizão, R. C. C., Marrs, R. H., Scott, D. A., and Viana, V. (1998). Rain forest on Maracá Island, Roraima, Brazil: soil and litter process response to artificial gaps. Forest Ecology and Management, 102, 291–303CrossRefGoogle Scholar
Luizão, R. C. C. (1994). Soil Biological Studies in Contrasting Types of Vegetation in Central Amazonian Forests. Unpublished Ph. D. thesis, University of Stirling, U.K.
Lüttge, U. (1997). Physiological Ecology of Tropical Plants. London: Springer
Malmer, A. (1993). Dynamics of Hydrology and Nutrient Losses as Response to Establishment of Forest Plantation. A Case Study on Tropical Rainforest land in Sabah, Malaysia. Lund, Sweden: Department of Forest Ecology, Swedish University of Agricultural Sciences
Manokaran, N. (1980). The nutrient contents of precipitation, throughfall and stemflow in a lowland tropical rainforest in peninsular Malaysia. Malaysian Forester, 43, 266–289Google Scholar
Marrs, R. H., Proctor, J., Heaney, A., and Mountford, M. D. (1988). Changes in soils, nitrogen mineralization and nitrification along an altitudinal transect in tropical rainforest in Costa Rica. Journal of Ecology, 58, 297–299Google Scholar
Marrs, R. H., Thompson, J., Scott, D., and Proctor, J. (1991). Nitrogen mineralization and nitrification in ‘terra firme’ forest and savanna soils on Ilha de Maracá, Roraima, Brazil. Journal of Tropical Ecology, 7, 123–137CrossRefGoogle Scholar
Marschner, H. (1991). Mechanism of adaptation of plants to acid soils. Plant and Soil, 134, 1–20CrossRefGoogle Scholar
Marschner, H. (1995). Mineral Nutrition of Higher Plants, 2nd edn. London: Academic Press
Masunaga, T., Kubota, D., Hotta, M., Shinmura, Y., and Wakatsuki, T. (1998a). Distribution characteristics of mineral elements in trees of tropical rainforest, West Sumatra, Indonesia. In Soils of Tropical Forest Ecosystems, ed. A. Schulte and D. Ruhiyat, pp. 168–174. Berlin: Springer
Masunaga, T., Kubota, D., Hotta, M., and Wakatsuki, T. (1997). Nutritional characteristics of mineral elements in leaves of tree species in tropical rainforest, west Sumatra, Indonesia. Soil Science and Plant Nutrition, 43, 405–418CrossRefGoogle Scholar
Masunaga, T., Kubota, D., Hotta, M., and Wakatsuki, T. (1998b). Nutritional characteristics of mineral elements in leaves of tree species in tropical rainforest, west Sumatra, Indonesia. Soil Science and Plant Nutrition, 44, 315–329CrossRefGoogle Scholar
McClain, M. E. and Elsenbeer, H. (2001). Terestrial inputs to Amazon streams and internal biogeochemical processing. In The Biogeochemistry of the Amazon Basin and its Role in a Changing World, ed. M. E. McClain, R. L. Victoria, and J. E. Richey, pp. 185–208. Oxford: Oxford University Press
Meir, P., Grace, J., and Miranda, A. C. (2001). Leaf respiration in two tropical rainforests: constraints on physiology by phosphorus, nitrogen and temperature. Functional Ecology, 15, 378–387CrossRefGoogle Scholar
Mengel, K., and Arneke, W. W. (1982). Effect of potassium on the water potential, the pressure potential, the osmotic potential and cell elongation in leaves of Phaseolus vulgaris. Physiologia Plantarum, 54, 402–408CrossRefGoogle Scholar
Minshall, W. H. (1975). Stimulation of transpiration by nitrogenous materials. Canadian Journal of Botany, 53, 1259–1263CrossRefGoogle Scholar
Mirmanto, E., Proctor, J., Green, J., Nagy, L., and Suriantata., (1999). Effects of nitrogen and phosphorus fertilization in a lowland evergreen rainforest. Philosophical Transactions of the Royal Society B, 354, 1825–1829CrossRefGoogle Scholar
Moyersoen, B., Alexander, I. J., and Fitter, A. H. (1998). Phosphorus nutrition of ectomycorrhizal and arbuscular mycorrhizal tree seedlings from a lowland tropical rainforest in Korup National Park, Cameroon. Journal of Tropical Ecology, 14, 47–61CrossRefGoogle Scholar
Nadkarni, N. M. (1986). The nutritional effects of epiphytes on host trees with special reference to alteration of precipitation chemistry. Selbyana, 9, 44–51Google Scholar
Nepstad, D. C., Carvalho, C. R., Davison, E. A., Jipp, P. H., Lefebvre, P. A., Negreiros, G. H., da Silva, E. D., Stone, T. A., Trumbore, S. E., and Vieira, S. (1994). The role of deep roots in the hydrological and carbon cycles of Amazonian forests and pastures. Nature, 372, 666–669CrossRefGoogle Scholar
Newbery, D. M., Alexander, I. J., and Rother, J. A. (1997). Phosphorus dynamics in a lowland African rainforest; the influence of ectomycorrhizal trees. Ecological Monographs, 67, 367–409Google Scholar
Noij, I. G. A. M., Janssen, B. H., Wesselink, L. G., et al. (1993). Modelling Nutrient and Moisture Cycling in Tropical Forests. Wageningen, The Netherlands: Tropenbos Foundation
Nooren, C. A. M., Breemen, N., Stoorvogel, J. J.., (1995). The role of earthworms in the formation of sandy surface soils in a tropical forest in Ivory Coast. Geoderma, 65, 135–148CrossRefGoogle Scholar
Nortcliff, S. and Thornes, J. B. (1989). Variations in soil nutrients in relation to soil moisture status in a tropical forested ecosystem. In Mineral Nutrients in Tropical Forest and Savanna Ecosystems, ed. J. Proctor, pp. 43–54. Oxford: Blackwell Scientific Publications
Northup, R. R., Dahlgren, R. A. and Yu, Z. (1995). Intraspecific variation of conifer phenolic concentration on a marine terrace acidity gradient: a new interpretation. Plant and Soil, 171, 255–262CrossRefGoogle Scholar
Nussbaum, R., Anderson, J., and Spencer, T. (1995). Factors limiting the growth of indigenous tree seedlings planted on degraded rainforest soils in Sabah, Malaysia. Forest Ecology and Management, 74, 149–159CrossRefGoogle Scholar
Nye, P. H. (1961). Organic matter and nutrient cycles under moist tropical forest. Plant and Soil, 13, 334–346Google Scholar
Nye, P. H. and Tinker, P. B. (1977). Solute Movements in the Root-Soil System. Oxford: Blackwell Scientific Publications
Nykvist, N. (1998). Logging can cause a serious lack of calcium in tropical rainforest ecosystems: an example from Sabah, Malaysia. In Soils of Tropical Forest Ecosystems, ed. A. Schulte and D. Ruhiyat, pp. 87–91. Berlin: SpringerCrossRef
Oliveira-Filho, A. T., Vilela, E. A., Carvalho, D. A., and Gavilanes, M. L. (1994). Effects of soils and topography on the distribution of tree species in a tropical riverine forest in south-eastern Brazil. Journal of Tropical Ecology, 10, 483–588CrossRefGoogle Scholar
Oliveira-Filho, A. T., Ratter, J. A. and Shepherd, G. J. (1990). Floristic composition and community structure of a central Brazilian gallery forest. Flora, 184, 103–117CrossRefGoogle Scholar
Parker, G. G. (1983). Throughfall and stemflow in the forest nutrient cycle. Advances in Ecological Research, 13, 57–133CrossRefGoogle Scholar
Poels, R. L. H. (1987). Soils, Water and Nutrients in a Forest Ecosystem in Suriname. Wageningen, The Netherlands: Agricultural University
Proctor, J. (1983). Tropical forest litterfall. I. Problems of data comparison. In Tropical Rain Forest: Ecology and Management, eds. S. L. Sutton, T. C. Whitmore and A. C. Chadwick, pp. 267–273. Oxford: Blackwell Scientific Publications
Proctor, J. (1984). Tropical Forestlitterfall. II. The data set. In Tropical Rain Forest: The Leeds Symposium, eds. A. C. Chadwick and S. L. Sutton, pp. 83–113. Leeds: Leeds Philosophical and Literary Society
Proctor, J. (1987). Nutrient cycling in primary and old secondary rainforests. Applied Geography, 7, 135–152CrossRefGoogle Scholar
Proctor, J. (1995). Rainforests and their soils. In Ecology, Conservation, and Management of South-East Asian Rainforests, ed. R. B. Primack and T. E. Lovejoy, T. E. (eds) pp. 87–104. London: Yale University PressCrossRef
Proctor, J. (1999). Heath forests and acid soils. Botanical Journal of Scotland, 51, 1–14CrossRefGoogle Scholar
Proctor, J., Baker, A. J. M., Bruijnzeel, L. A., Balgooy, M. M. J., Fairweather, G. M., and Madulid, D. A. (2000). Foliar chemistry and leaf herbivory on Mount Bloomfield, Palawan, Philippines. Botanical Journal of Scotland, 52, 79–89CrossRefGoogle Scholar
Raaimakers, D., Boot, R. G. A., Dijkstra, P., Pot, S., and Pons, T. (1995). Photosynthetic rates in relation to leaf phosphorus content in pioneer versus climax tropical rainforest trees. Oecologia, 102, 120–125CrossRefGoogle ScholarPubMed
Raich, J. W., Riley, R. H., and Vitousek, P. M. (1994). Use of root-ingrowth cores to assess nutrient limitations in forest ecosystems. Canadian Journal of Forest Research, 24, 2135–2138CrossRefGoogle Scholar
Ratter, J. A. (1980). Notes on the Vegetation of Fazenda Agua Limpa (Brasilia, DF, Brazil). Edinburgh: Royal Botanic Gardens
Raven, J. A. (1983). The transport and function of silicon in plants. Biological Reviews, 58, 179–207CrossRefGoogle Scholar
Reich, P. B., Walters, M. B., Ellsworth, D. S.et al. (1994). Photosynthesis – nitrogen relations in Amazonian tree species. I. Patterns among species and communities. Oecologia 97, 62–72CrossRefGoogle ScholarPubMed
Rice, E. I. and Pancholy, S. K. (1973). Inhibition of nitrification by climax ecosystems II. Additional evidence and possible role of tannins. American Journal of Botany, 60, 691–702CrossRefGoogle Scholar
Riddoch, I., Lehto, T., and Grace, J. (1991). Photosynthesis of tropical tree seedlings in relation to light and nutrient supply. New Phytologist, 137–147CrossRefGoogle Scholar
Robertson, G. P. (1984). Nitrification and and nitrogen mineralization in a lowland rainforest succession in Costa Rica. Oecologia, 61, 99–104CrossRefGoogle Scholar
Robertson, G. P. (1989). Nitrification and denitrification in humid tropical ecosystems: potential controls of nitrogen retention. In Mineral Nutrients in Tropical Forest and Savanna Ecosystems, ed. J. Proctor, pp. 55–69. Oxford: Blackwell Scientific Publications
Robertson, G. P. and Tiedje, J. M. (1988). Denitrification in lowland tropical rainforest. Nature, 336, 756–759CrossRefGoogle Scholar
Roggy, J. C., Prevost, M. F., Garbaye, J. and Domenach, A. M. (1999). Nitrogen cycling in the tropical rainforest of French Guiana: comparison of two sites with contrasting soil types using δ15N. Journal of Tropical Ecology, 15, 1–22CrossRefGoogle Scholar
Roy, S. and Singh, J. S. (1995). Seasonal and spatial dynamics of plant-available N and P pools and N-mineralization in relation to fine roots in dry tropical forest habitat. Soil Biology and Biochemistry 27, 33–40CrossRefGoogle Scholar
Russell, R. S. (1974). Plant Root Systems. London: McGraw-Hill
Sands, R. and Mulligan, D. R. (1990). Water and nutrient dynamics and tree growth. Forest Ecology and Management, 30, 91–111CrossRefGoogle Scholar
Scatena, F. N., Silver, W., Siccama, T., Johnson, A. and Sanchez, M. J. (1993). Biomass and nutrient content of the Bisley experimental watersheds, Luquillo experimental forest, Puerto Rico, before and after Hurricane Hugo, 1989. Biotropica, 25, 15–27CrossRefGoogle Scholar
Scott, D. A., Proctor, J. and Thompson, J. (1992). Ecological studies on a lowland evergreen rainforest on Maracá Island, Roraima, Brazil. II. Litter and nutrient cycling. Journal of Ecology, 80, 705–717CrossRefGoogle Scholar
Silver, W., Lugo, A. E. and Keller, M. (1999). Soil oxygen availability and biogeochemistry along rainfall and topographic gradients in upland wet tropical forest soils. Biogeochemistry, 44, 301–328CrossRefGoogle Scholar
Silver, W., Scatena, F. N., Johnson, A. H., Siccama, T. G., and Sanchez, M. J. (1994). Nutrient availability in wet montane forest: spatial patterns and methodological considerations. Plant and Soil, 164, 129–145CrossRefGoogle Scholar
Smirnoff, N. and Stewart, G. R. (1985). Nitrate assimilation and translocation by higher plants: comparative physiology and ecological consequences. Physiologia Plantarum, 64, 133–140CrossRefGoogle Scholar
Smirnoff, N., Todd, P. and Stewart, G. R. (1984). The occurrence of nitrate reduction in the leaves of woody plants. Annals of Botany, 54, 363–374CrossRefGoogle Scholar
Smith, C. K., Gholz, H. L., and Assis Oliveira, F. (1998). Fine litter chemistry, early-stage decay, and nitrogen dynamics under plantations and primary forest in lowland Amazonia. Soil Biology and Biochemistry, 30, 2159–2169CrossRefGoogle Scholar
Smits, W. T. M. (1994). Dipterocarpaceae: Mycorrhizae and Regeneration. The Netherlands, Wageningen: The Tropenbos Foundation
Sobrado, M. and Medina, E. (1980). General morphology, anatomical structure and nutrient content of sclerophyllous leaves of the ‘Bana’ vegetation of Amazonia. Oecologia, 45, 341–345CrossRefGoogle Scholar
Soil Survey Staff (1975). Soil Taxonomy: A Basic System of Soil Classification for Making and Interpreting Soil Surveys, Agricultural Handbooks no. 436. Washington, D.C.: United States Department of Agriculture
Sollins, P. (1989). Factors affecting nutrient cycling in tropical soils. In Mineral Nutrients in Tropical Forest and Savanna Ecosystems, ed. J. Proctor, pp. 85–95. Oxford: Blackwell Scientific Publications
Sollins, P. (1998). Factors influencing species composition in tropical lowland rainforest: does soil matter?Ecology, 79, 23–30CrossRefGoogle Scholar
Sollins, P. and Radulovich, R. (1988). Effects of soil physical structure on solute transport in a weathered tropical soil. Soil Science Society of America Journal, 52, 1168–1173CrossRefGoogle Scholar
Sprent, J. I. (1995). Legume trees and shrubs in the tropics: N2 fixation in perspective. Soil Biology and Biochemistry, 27, 401–407CrossRefGoogle Scholar
Sprent, J. I. and Raven, J. I. (1985). Evolution of nitrogen fixing symbioses. Proceedings of the Royal Society of Edinburgh, 85B, 215–237Google Scholar
Steinhardt, U. (1979). Untersuchungen über den Wasser- und Nährstoffhaushalt eines andinen Wolkenwoldes in Venezuela. Göttinger Bodenkundliche Berichte no. 56Google Scholar
Stewart, G. R., Joly, C. A., and Smirnoff, N. (1992). Partitioning of organic nitrogen assimilation between roots and shoots of cerrado and forest trees of contrasting plant communities of South East Brazil. Oecologia, 91, 511–517CrossRefGoogle Scholar
Tanner, E. V. J. (1977). Mineral Cycling in Montane Rain Forests in Jamaica. Unpublished Ph. D. thesis, University of Cambridge
Tanner, E. V. J. (1980). Studies on the biomass and productivity in a series of montane rain forests in Jamaica. Journal of Ecology, 68, 573–588CrossRefGoogle Scholar
Tanner, E. V. J. (1985). Jomaican montane forests: nutrient capital and cost of growth. Journal of Ecology, 73, 553–568CrossRefGoogle Scholar
Tanner, E. V. J., Vitousek, P. M. and Cuevas, E. (1998). Experimental investigation of nutrient limitation of forest growth on wet tropical mountains. Ecology, 79, 10–22CrossRefGoogle Scholar
Thompson, J., Proctor, J., Viana, V., Milliken, W., Ratter, J. A., and Scott, D. A. (1992). Ecological studies on a lowland evergreen rainforest on Maracá Island, Roraima, Brazil. 1. Physical environment, forest structure and leaf chemistry. Journal of Ecology, 80, 689–703CrossRefGoogle Scholar
Turner, I. M., Brown, N. D., and Newton, A. C. (1993). Effect of fertilizer application on dipterocarp seedling growth and mycorrhizal infection. Forest Ecology and Management, 57, 329–337CrossRefGoogle Scholar
Tyler, G. (1994). Plant uptake of aluminium from calcareous soils. Experientia, 50, 701–703CrossRefGoogle Scholar
Breemen, N., Finlay, R., Lundstrom, U., Jongmans, A. G., Giesler, R., and Olsson, M. (2000). Mycorrhizal weathering: a true case of mineral plant nutrition. Biogeochemistry 49: 53–67CrossRefGoogle Scholar
Van Dam, O. (2001). Forest Filled with Gaps. The Netherlands: University of Utrecht
Schaik, C. P. and Mirmanto, E. (1985). Spatial variation in the structure and litterfall of a Sumatran rainforest. Biotropica, 17, 196–205CrossRefGoogle Scholar
Veneklaas, E. J.(1990). Rainfall Interception and Aboveground Nutrient Fluxes in Colombian Montane Tropical Rain Forests. The Netherlands: Utrecht, Rijksuniversitheit
Villela, D. M. and Proctor, J. (2002). Leaf litter decomposition and monodominance in the Peltogyne forest of Maracá Island, Brazil. Biotropica, 34, 334–347Google Scholar
Vitousek, P. M. (1984). Litterfall, nutrient cycling, and nutrient limitation in tropical forests. Ecology, 65, 285–298CrossRefGoogle Scholar
Vitousek, P. M. and Sanford, R. L. (1986). Nutrient cycling in moist tropical forest. Annual Review of Ecology and Systematics, 17, 137–167CrossRefGoogle Scholar
Vitousek, P. M., Walker, L. R., Whiteaker, l. D., and Matson, P. A. (1993). Nutrient limitations to plant growth during primary succession in Hawaii Volcanoes National Park. Biogeochemistry, 23, 197–215CrossRefGoogle Scholar
Walker, T. W. and Syers, J. K. (1976). The fate of phosphorus during pedogenesis. Geoderma, 15, 1–19CrossRefGoogle Scholar
Waterloo, M. J. (1994). Water and Nutrient Dynamics of Pinus caribea Plantation Forests on Former Grassland Soils in Southwest Viti Levu, Fiji. Ph. D. thesis, The Netherlands: Vrije Universität, Amsterdam
Waterloo, M. J., Schelleken, J., Bruijnzeel, L. A.., (1997). Chemistry of bulk precipitation in southwestern Viti Levu, Fiji. Journal of Tropical Ecology, 13, 427–447CrossRefGoogle Scholar
Went, F. W. and Stark, N. (1968a) Mycorrhiza. BioScience, 18, 1035–1039CrossRefGoogle Scholar
Went, F. W. and Stark, N. (1968b). The biological and mechanical role of the soil fungi. Proceedings of the National Academy of Sciences of the USA, 60, 497–504CrossRefGoogle Scholar
Westman, W. E. (1978). Inputs and cycling of mineral nutrients in a coastal subtropical eucalypt forest. Journal of Ecology, 66, 513–531CrossRefGoogle Scholar
Whitmore, T. C. (1984). Tropical Rain Forests of the Far East. Oxford: Clarendon Press
Wieder, W. and Wright, S. J. (1995). Tropical forest litter dynamics and dry season irrigation on Barro Colorado Island, Panama. Ecology, 76, 1971–1979CrossRefGoogle Scholar
Wild, A. (1989). Mineral nutrients in tropical ecosystems: a soil scientist's view. In Mineral Nutrients in Tropical Forest and Savanna Ecosystems, ed. J. Procter, pp. 441–456. Oxford: Blackwell Scientific Publications
Wyn Jones, R. G. and Lunt, O. R. (1967). The function of calcium in plants. Botanical Reviews, 33, 407–426CrossRefGoogle Scholar
Yap, S. W. (1998). Large Scale Enrichment Planting of Dipterocarps in Logged-Over Forests in Sabah, Malaysia: Potential Role of Fertiliser Application. Unpublished Ph. D thesis, University of London
Yavitt, J. B. and Wright, S. J. (1996). Temporal patterns of soil nutrients in a Panamanian moist forest revealed by ion-exchange resin and experimental irrigation. Plant and Soil, 183, 117–129CrossRefGoogle Scholar
Zimmerman, C. F., Price, M. T. and Montgomery, J. R. (1978). A comparison of ceramic cup and teflon in situ samplers for nutrient pore water determinations. Estuarine, Coastal and Marine Sciences, 6, 93–97CrossRefGoogle Scholar

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