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45 - Is there evidence for limitations to nitrogen mineralization in upper montane tropical forests?

from Part IV - Nutrient dynamics in tropical montane cloud forests

Published online by Cambridge University Press:  03 May 2011

By
W. L. Silver ,
A. W. Thompson ,
D. J. Herman  and
M. K. Firestone
Edited by
L. A. Bruijnzeel ,
F. N. Scatena  and
L. S. Hamilton
W. L. Silver
Affiliation:
University of California, USA
A. W. Thompson
Affiliation:
University of California, USA
D. J. Herman
Affiliation:
University of California, USA
M. K. Firestone
Affiliation:
University of California, USA
L. A. Bruijnzeel
Affiliation:
Vrije Universiteit, Amsterdam
F. N. Scatena
Affiliation:
University of Pennsylvania
L. S. Hamilton
Affiliation:
Cornell University, New York
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Summary

ABSTRACT

The structure and function of forest ecosystems often change along altitudinal gradients in the tropics, culminating in short-stature, low-productivity cloud forests at the uppermost elevations. Field data and literature values were used to examine patterns in nitrogen mineralization on tropical mountains and to discuss the potential for nitrogen limitation to net primary productivity. Few trends in net nitrogen mineralization within and across elevation gradients in the tropics were found, and rates were generally comparable to those found in tropical forests at low elevations. Gross nitrogen mineralization rates were much higher than net rates, and in Puerto Rico upper montane forests exhibited higher gross nitrogen mineralization than lower elevation forests. Work from Puerto Rico found no effect of short-term anaerobic conditions. In Hawai'i gross nitrogen mineralization increased with substrate age. Ammonium availability was augmented by dissimilatory nitrate reduction to ammonium in montane forests; nitrogen conservation via this pathway exceeded losses via N2O production. Patterns in nitrogen circulation in upper montane forests in Puerto Rico showed that elfin and palm forests had lower nitrogen use efficiency and a higher proportion of nitrogen mineralized from decomposing litter relative to other forest types, further indicating that rates of nitrogen supply in these forests are considerable. In summary, the data reviewed in this chapter suggest that nitrogen limitation alone cannot explain patterns in the structure and function of tropical montane forest vegetation. Alternative factors are offered that warrant further investigation.

Type
Chapter
Information
Tropical Montane Cloud Forests
Science for Conservation and Management
 , pp. 418 - 427
Publisher: Cambridge University Press
Print publication year: 2011

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References

Brown, S., Lugo, A. E., Silander, S., and Liegal, L. (1983). Research History and Opportunities in the Luquillo Experimental Forest, General Technical Report No. SO-441. New Orleans, LA: U.S. Department of Agriculture-Forest Service Southern Forest Experimental Station.CrossRefGoogle Scholar
Bruijnzeel, L. A., and Proctor, J. (1995). Hydrology and biogeochemistry of tropical montane cloud forests: what do we really know? In Tropical Montane Cloud Forests, eds. Hamilton, L. S., Jarvik, J. O., and Scatena, F. N., pp. 38–78. New York: Springer-Verlag.CrossRefGoogle Scholar
Buss, H. L., White, A. F., Vivit, D., et al. (2008). Mineral weathering in a deep volcaniclastic saprolite, Luquillo Mountains, Puerto Rico. Geochimica et Cosmochimica Acta 72: 124–133.Google Scholar
Cavelier, J., Tanner, E., and Santamaria, J. (2000). Effect of water, temperature and fertilizers on soil nitrogen net transformations and tree growth in an elfin cloud forest of Columbia. Journal of Tropical Ecology 16: 83–99.CrossRefGoogle Scholar
Cicerone, R. J. (1987). Changes in stratospheric ozone. Science 237: 35–42.CrossRefGoogle ScholarPubMed
García-Martinó, A. R., Warner, G. S., Scatena, F. N., and Civco, D. L. (1996). Rainfall, runoff and elevation relationships in the Luquillo Mountains of Puerto Rico. Caribbean Journal of Science 32: 413–424.Google Scholar
Groffman, P. M., and Tiedje, J. M. (1989). Denitrification in north temperate forest soils: spatial and temporal patterns at the landscape and seasonal scales. Soil Biology and Biochemistry 21: 613–620.CrossRefGoogle Scholar
Grubb, P. J. (1977). Control of forest growth and distribution on wet tropical mountains: with special reference to mineral nutrition. Annual Review of Ecology and Systematics 8: 83–107.CrossRefGoogle Scholar
Hafkenscheid, R. L. L. J. (2000). Hydrology and biogeochemistry of tropical montane rain forests of contrasting stature in the Blue Mountains, Jamaica. Ph.D. thesis, VU University Amsterdam, Amsterdam, the Netherlands. Also available at http://dare.ubvu.vu.nl/bitstream/1871/12734/1/tekst.pdf.Google Scholar
Hall, S. J., and Matson, P. A. (2003). Nutrient status of tropical rain forests influences soil N dynamics after N additions. Ecological Monographs 73: 107–129.CrossRefGoogle Scholar
Hart, S. C., Stark, J. M., Davidson, E. A., and Firestone, M. K. (1994). Nitrogen mineralization, immobilization, and nitrification. In Methods of Soil Analysis, Part 2, Microbiological and Biochemical Properties, ed. Weaver, R. W., pp. 985–1018. Madison, WI: Soil Science Society of America.Google Scholar
Herman, D. J., Brooks, P. D., Ashraf, M., Azam, F., and Mulvaney, R. L. (1995). Evaluation of methods for nitrogen-15 analysis of inorganic nitrogen in soil extracts. II. Diffusion methods. Communications in Soil Science and Plant Analysis 26: 1675–1685.CrossRefGoogle Scholar
Holwerda, F., Burkard, R., Eugster, W. E., et al. (2006). Estimating fog deposition at a Puerto Rican elfin cloud forest site: comparison of the water budget and eddy covariance methods. Hydrological Processes 20: 2669–2692.CrossRefGoogle Scholar
Keller, M., Kaplan, W. A., and Wofsy, S. C. (1986). Emissions of N2O, CH4, and CO2 from tropical forest soils. J. Geophys. Res. 91: 11 791–11 802.CrossRefGoogle Scholar
Kiese, R., Papen, H., Zumbusch, E., and Butterbach-Bahl, K. (2002). Nitrification activity in tropical rain forest soils of the Coastal Lowlands and Atherton Tablelands, Queensland, Australia. Journal of Plant Nutrition and Soil Science 165: 682–685.CrossRefGoogle Scholar
Kirkham, D., and Bartholomew, W. V. (1954). Equations for following nutrient transformations in soil, utilizing tracer data. Soil Science Society of America Proceedings 18: 33–34.CrossRefGoogle Scholar
Kitayama, K., and Aiba, S. (2002). Ecosystem structure and productivity of tropical rain forests along altitudinal gradients with contrasting soil phosphorus pools on Mount Kinabalu, Borneo. Journal of Ecology 90: 37–51.CrossRefGoogle Scholar
Lashof, D. A., and Ahuja, D. R. (1990). Relative contributions of greenhouse gas emissions to global warming. Nature 344: 529–531.CrossRefGoogle Scholar
Leuschner, Ch., Moser, G., Bertsch, C., Röderstein, M., and Hertel, D. (2007). Large altitudinal increase in tree root/shoot ratio in tropical mountain forests of Ecuador. Basic and Applied Ecology 8: 219–230.CrossRefGoogle Scholar
Marrs, R. H., Proctor, J., Heaney, A., and Mountford, M. D. (1988). Changes in soil nitrogen mineralization and nitrification along an altitudinal transect in tropical rain forest in Costa Rica. Journal of Ecology 76: 466–482.CrossRefGoogle Scholar
McDowell, W., and Asbury, C. (1994). Export of carbon, nitrogen, and major ions from three tropical montane watersheds. Limnology and Oceanography 39: 111–125.CrossRefGoogle Scholar
McGroddy, M. and Silver, W. L. (2000). Variations in belowground carbon storage and soil CO2 flux rates along a wet tropical climate gradient. Biotropica 32: 614–624.CrossRefGoogle Scholar
Moser, G., Hertel, D., and Leuschner, C h. (2007). Altitudinal change in LAI and stand leaf biomass in tropical montane forests: a transect study in Ecuador and a pan-tropical meta-analysis. Ecosystems 10: 924–935.CrossRefGoogle Scholar
Myrold, D. D. (1998). Microbial nitrogen transformations. In Principles and Applications of Soil Microbiology, eds. Sylvia, D. M., Fuhrmann, J. J., Hartel, P. G., and Zuberer, D. A., pp. 259–294. Upper Saddle River, NJ: Prentice Hall.Google Scholar
Pett-Ridge, J., and Firestone, M. K. (2005). Redox fluctuation structures microbial community in a wet tropical soil. Applied and Environmental Microbiology, 71: 6998–7007.CrossRefGoogle Scholar
Pett-Ridge, J., Silver, W. L., and Firestone, M. K. (2006). Redox fluctuations in a humid tropical forest soil impact N-cycling rates by framing the composition of the soil microbial community. Biogeochemistry 81: 95–110.CrossRefGoogle Scholar
Píco, R. (1974). The Geography of Puerto Rico. Chicago, IL: Aldine.Google Scholar
Raich, J. W., Russell, A. E., and Vitousek, P. M. (1997). Primary productivity and ecosystem development along an elevational gradient on Mauna Loa, Hawai'i. Ecology 78: 707–721.Google Scholar
Riley, R. H., and Vitousek, P. M. (1995). Nutrient dynamics and nitrogen trace gas flux during ecosystem development in montane rain forest. Ecology 76: 292–304.CrossRefGoogle Scholar
Santiago, L. S., Goldstein, G., Meinzer, F. C., Fownes, J. H., and Mueller-Dombois, D. (2000). Transpiration and forest structure in relation to soil waterlogging in a Hawaiian montane cloud forest. Tree Physiology 20: 673–681.CrossRefGoogle Scholar
Schimel, J. P., and Bennett, J. (2004). Nitrogen mineralization: challenges of a changing paradigm. Ecology 85: 591–602.CrossRefGoogle Scholar
Schuur, E. (2001). The effect of water on decomposition dynamics in mesic to wet Hawaiian montane forests. Ecosystems 4: 259–273.CrossRefGoogle Scholar
Schuur, E. A. G., Chadwick, O. A., and Matson, P. A. (2001). Carbon cycling and soil carbon storage in mesic to wet Hawaiian montane forests. Ecology 82: 3182–3196.CrossRefGoogle Scholar
Silver, W. (1994). Is nutrient availability related to plant nutrient use in humid tropical forests?Oecologia 98: 336–343.CrossRefGoogle ScholarPubMed
Silver, W. L., Keller, M., and Lugo, A. E. (1999). Soil oxygen availability and biogeochemical cycling along elevation and topographic gradients in Puerto Rico. Biogeochemistry 44: 301–328.CrossRefGoogle Scholar
Silver, W. L., Herman, D. J., and Firestone, M. K. (2001). Dissimilatory nitrate reduction to ammonium in upland tropical forest soils. Ecology 82: 2410–2416.CrossRefGoogle Scholar
Silver, W. L., Thompson, A. W., Firestone, M. K., Reich, A., and Ewel, J. J. (2005). Nitrogen retention and loss in tropical plantations and old growth forests. Ecological Applications 15: 1604–1614.CrossRefGoogle Scholar
Soethe, N., Lehmann, J., and Engels, C. (2006). The vertical pattern of rooting and nutrient uptake at different altitudes of a south Ecuadorian montane forest. Plant and Soil 286: 287–299.CrossRefGoogle Scholar
Soethe, N., Lehmann, J., and Engels, C. (2008a). Nutrient availability at different altitudes in a tropical montane forest in Ecuador. Journal of Tropical Ecology 24: 397–406.CrossRefGoogle Scholar
Soethe, N., Wilcke, W., Homeier, J., Lehmann, J., and Engels, C. (2008b). Plant growth along the altitudinal gradient: role of plant nutritional status, fine root activity, and soil properties. In Gradients in a Tropical Mountain Ecosystem of Ecuador, eds. Beck, E., Bendix, J., Kottke, I., Makeschin, F., and Mosandl, R., pp. 259–266. Berlin: Springer-Verlag.CrossRefGoogle Scholar
Tanner, E. V. J. (1977). Four montane rain forests of Jamaica: a quantitiative characterization of the floristics, the soils and the foliar mineral levels, and a discussion of the interrelations. Journal of Ecology 65: 883–918.CrossRefGoogle Scholar
Tanner, E. V. J., Kapos, V., Freskos, S., Healey, J. R., and Theobald, A. M. (1990). Nitrogen and phophorus fertilization of Jamaican montane forest trees. Journal of Tropical Ecology 6: 231–238.CrossRefGoogle Scholar
Tanner, E. V. J., Kapos, V., and Franco, W. (1992). Nitrogen and phosphorus fertilization effects on Venezuelan montane forest trunk growth and litterfall. Ecology 73: 78–86.CrossRefGoogle 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: 10–22.CrossRefGoogle Scholar
Templer, P. H., Silver, W. L., Pett-Ridge, J., DeAngelis, K., and Firestone, M. K. (2008). Plant and microbial controls on nitrogen retention and loss in a humid tropical forest. Ecology 89: 3030–3040.CrossRefGoogle Scholar
Tiedje, J. M., Sexton, A. J., Myrold, D. D., and Robinson, J. A. (1982). Denitrification: ecological niches, competition and survival. Antonie van Leeuwenhoeck 48: 569–583.CrossRefGoogle Scholar
Vitousek, P. (1982). Nutrient cycling and nutrient use efficiency. American Naturalist 119: 553–572.CrossRefGoogle Scholar
Vitousek, P. (1984). Litterfall, nutrient cycling, and nutrient limitation in tropical forests. Ecology 65: 285–298.CrossRefGoogle Scholar
Vitousek, P. M., and Farrington, H. (1997). Nutrient limitation and soil development: experimental test of a biogeochemical theory. Biogeochemistry 37: 63–75.CrossRefGoogle Scholar
Vitousek, P. M., and Matson, P. A. (1988). Nitrogen transformations in a range of tropical forest soils. Soil Biology and Biochemistry 20: 361–367.CrossRefGoogle Scholar
Vitousek, P. M., Matson, P. A., and Turner, D. R. (1988). Elevational and age gradients in Hawaiian montane rainforest: foliar and soil nutrients. Oecologia 84: 362–370.CrossRefGoogle 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: 197–215.CrossRefGoogle Scholar
Weaver, P. L. (1994). Bano de Oro Natural Area Luquillo Mountains, Puerto Rico. New Orleans, LA: U.S. Department of Agriculture Forest Service Southern Forest Experiment Station.CrossRefGoogle Scholar
Weaver, P. L. (1995). The Colorado and dwarf forests of Puerto Rico's Luquillo Mountains. In Tropical Forests: Management and Ecology, eds. Lugo, A. E. and Lowe, C., pp. 109–141. New York: Springer-Verlag.CrossRefGoogle Scholar
Wieder, R. K., and Lang, G. E. (1982). A critique of the analytical methods used in examining decomposition data obtained from litter bags. Ecology 63: 1636–1642.CrossRefGoogle Scholar
Wilkinson, L. (1984). Systat, Version 1. Evanston, IL: Systat Inc.

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