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49 - Environmental controls on photosynthetic rates of lower montane cloud forest vegetation in south-western Colombia

from Part V - Cloud forest water use, photosynthesis, and effects of forest conversion

Published online by Cambridge University Press:  03 May 2011

By
M. G. Letts ,
M. Mulligan ,
M. E. Rincón-Romero  and
L.A. Bruijnzeel
Edited by
L. A. Bruijnzeel ,
F. N. Scatena  and
L. S. Hamilton
M. G. Letts
Affiliation:
University of Lethbridge, Canada
M. Mulligan
Affiliation:
King's College London, UK
M. E. Rincón-Romero
Affiliation:
Universidad del Valle, Colombia
L.A. Bruijnzeel
Affiliation:
VU University, Netherlands
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

A variety of microclimatic and edaphic factors have been shown to limit photosynthetic productivity in tropical montane cloud forest (TMCF) ecosystems. It is now understood that multiple controls may limit photosynthesis within individual TMCFs, and that the relative importance of each control varies between sites. This chapter describes the nutrient status, micro-climate, leaf structural traits and photosynthetic gas-exchange characteristics of lower montane cloud forest (LMCF) vegetation at the Centro de Estudios Ambientales Tambito site, a wet LMCF reserve located on the Pacific slopes of Colombia's Western Cordillera. Neither periodic water shortage nor prolonged waterlogging was observed at Tambito. Total soil nitrogen and available phosphorus were above the range typically observed in lowland evergreen rain forests (LERF), while exchangeable calcium levels were lower. In terms of soil nutrient status, total nitrogen and available phosphorus at Tambito were above the range typically observed in more productive LERF, while exchangeable calcium levels were lower. Leaf nutrient contents observed at Tambito were broadly similar to values observed in LERF. Photosynthetic photon flux density (PPFD) remained well below the light-saturation level for leaf-scale photosynthesis (A) throughout the day during the wet season and for 21 hours day−1 during the dry season. Cloudiness may reduce the competitive advantage of high Amax in canopy leaves, thereby increasing the fitness of alternative traits conferred by low specific leaf area, including nutrient-use efficiency and leaf longevity. Therefore, it was concluded that persistent PPFD limitation of photosynthesis may help to explain the prevalence of sclerophylly in tropical montane cloud forests.

Type
Chapter
Information
Tropical Montane Cloud Forests
Science for Conservation and Management
 , pp. 465 - 478
Publisher: Cambridge University Press
Print publication year: 2011

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References

Aerts, R., and Peijl, M. J. (1993). A simple model to explain the dominance of low productive perennials in nutrient-poor habitats. Oikos 66: 144–147.CrossRefGoogle Scholar
Bautista-Cruz, A., and del Castillo, R. F. (2005). Soil changes during secondary succession in a tropical montane cloud forest area. Soil Science Society of America Journal 69: 906–914.CrossRefGoogle Scholar
Benton, J. B., and Jones, J. (1989). Plant Analysis Techniques. Athens, GA: Benton–Jones Laboratories.Google Scholar
Boyce, R. L., McCune, D. C., and Berlyn, G. P. (1991). A comparison of foliar wettability of red spruce and balsam fir growing at high elevation. New Phytologist 117: 543–555.CrossRefGoogle Scholar
Brady, N. C., and Weil, R. R. (1999). The Nature and Properties of Soils, 12th edn. Upper Saddle River, NJ: Prentice Hall.Google Scholar
Bremmer, J. M., and Mulvaney, C. S.. (1982). Nitrogen-total. In Methods of Soil Analysis, Part 2, Chemical and Microbiological Properties, eds. Page, A. L., Miller, R. H., and Keeney, D. R., pp. 595–624. Madison, WI: American Society of Agronomy and Soil Science Society of America.Google Scholar
Brewer, C. A., and Smith, W. K. (1995). Leaf surface wetness and gas exchange in the pond lily Nuphar polysepalum (Nymphaeaceae). American Journal of Botany 82: 1271–1277.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., Juvik, J. O., and Scatena, F. N., pp. 38–78. New York: Springer-Verlag.CrossRefGoogle Scholar
Bruijnzeel, L. A., and Veneklaas, E. J. (1998). Climatic conditions and tropical montane forest productivity: the fog has not lifted yet. Ecology 79: 3–9.CrossRefGoogle Scholar
Bruijnzeel, L. A., Waterloo, M. J., Proctor, J., Kuiters, A. T., and Kotterink, B. (1993). Hydrological observations in montane rain forests on Gunung Silam, Sabah, Malaysia, with special reference to the ‘Massenerhebung’ effect. Journal of Ecology 81: 145–167.CrossRefGoogle Scholar
Cavelier, J. (1992). Fine-root biomass and soil properties in a semideciduous and a lower montane rain forest in Panama. Plant and Soil 142: 187–201.CrossRefGoogle Scholar
Cavelier, J., and Goldstein, G. (1989). Leaf anatomy and water relations in tropical elfin cloud forest tree species. In Structural and Functional Responses to Environmental Stresses, eds. Kreeb, K. H., Richter, H., and Hinckley, T. M., pp. 243–253. The Hague: SPB Academic Publishing.Google Scholar
Cavelier, J., and Mejía, C. (1990). Climatic factors and tree stature in the elfin cloud forest of Serrania de Macuira, Colombia. Agricultural and Forest Meteorology 53: 105–123.CrossRefGoogle Scholar
Devices, Delta-T (1999). Theta Probe Soil Moisture Sensor Type ML2x: User's Manual. Cambridge, UK: Delta-T Devices.Google Scholar
Dietz, J., Leuschner, Ch., Hölscher, D., and Kreilein, H. (2007). Vertical patterns and duration of surface wetness in an old-growth tropical montane forest, Indonesia. Flora 202: 111–117.CrossRefGoogle Scholar
Flenley, J. R. (1995). Cloud forest, the Massenerhebung effect, and ultraviolet insolation. In Tropical Montane Cloud Forests, eds. Hamilton, L. S., Juvik, J. O., and Scatena, F. N., pp. 150–155. New York: Springer-Verlag.CrossRefGoogle Scholar
Fogg, G. E. (1947). Quantitative studies on the wetting of leaves by water. Proceedings of the Royal Society of London Series B 134: 503–522.CrossRefGoogle ScholarPubMed
Gerold, G., Schawe, M., and Bach, K. (2008). Hydrometeorologic, pedologic, and vegetation patterns along an elevational transect in the montane forest of the Bolivian Yungas. Die Erde 139: 141–168.Google Scholar
Gerrish, G., Mueller-Dombois, D., and Bridges, K. W. (1988). Nutrient limitation and Metrosideros forest dieback in Hawaii. Ecology 69: 723–727.CrossRefGoogle Scholar
Goldberg, S. (1997). Reactions of boron with soils. Plant and Soil 193: 35–48.CrossRefGoogle Scholar
Goudriaan, J. (1977). Crop Micrometeorology: A Simulation Study. Wageningen, the Netherlands: PUDOC.Google Scholar
Graham, E. A., Mulkey, S. S., Kitajima, K., Phillips, N. G., and Wright, S. J. (2003). Cloud cover limits net CO2 uptake and growth of a rainforest tree during tropical rainy seasons. Proceedings of the National Academy of Sciences USA 100: 572–576.CrossRefGoogle ScholarPubMed
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
Herbert, D. A., and Fownes, J. H. (1999). Forest productivity and efficiency of resource use across a chronosequence of tropical montane soils. Ecosystems 2: 242–254.CrossRefGoogle Scholar
Holwerda, F. (2005). Water and energy budgets of rain forests along an elevation gradient under maritime tropical conditions. Ph.D. thesis, VU University Amsterdam, Amsterdam, the Netherlands. Also available at http://www.falw.vu.nl/nl/onderzoek/earth-sciences/geo-environmental-science-and-hydrology/hydrology-dissertations/index.asp.Google Scholar
John, R., Dalling, J. W., Harms, K. E., et al. (2007). Soil nutrients influence spatial distributions of tropical tree species. Proceedings of the National Academy of Sciences of the USA 104: 864–869.CrossRefGoogle ScholarPubMed
Jordan, C. F. (1985). Nutrient Cycling in Tropical Forest Ecosystems. Chichester, UK: John Wiley.Google Scholar
Kerr, A. C., Tarney, J., Nivia, A., Marriner, G. F., and Saunders, A. D. (1998). The internal structure of oceanic plateaus: Inferences from obducted Cretaceous terranes in western Colombia and the Caribbean. Tectonophysics 292: 173–188.CrossRefGoogle Scholar
Kitayama, K., and Aiba, S. I. (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
Lai, I. L., Schröder, W. H., Wu, J. T., et al. (2007). Can fog contribute to the nutrition of Chamaecyparis obtusa var. formosana? Uptake of a fog solute tracer into foliage and transport to roots. Tree Physiology 27: 1001–1009.CrossRefGoogle Scholar
Landsberg, J. J. (1986). Physiological Ecology of Forest Production. New York: Academic Press.Google Scholar
Letts, M. G. (2003). Carbon assimilation and productivity in a north-west Andean tropical montane cloud forest. Ph.D. thesis, King's College London, University of London, London, UK. Also available at http://people.uleth.ca/~matthew.letts/letts thesis 2003.pdf.Google Scholar
Letts, M. G., and Mulligan, M. (2005). The impact of light quality and leaf wetness on photosynthesis in north-west Andean tropical montane cloud forest. Journal of Tropical Ecology 21: 549–557.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
Linder, S. (1985). Potential and actual production in Australian forest stands. In Research for Forest Management, eds. Lansbery, J. J. and Parsons, W., pp. 11–35. Melbourne, Australia: CSIRO.Google Scholar
Mackean, S. (1993). Manual de análisis de suelos y plantas. Santiago de Cali, Colombia: Centro Internacional de Agricultura Tropical (CIAT).Google Scholar
Malhi, Y., Meir, P., Bird, M., Salinas, N., and Silman, M. (2006). Detailed Assessment of Ecosystem Carbon Dynamics along a Tropical Forest Altitudinal Gradient, research proposal to the National Environment Research Council of the UK. Oxford, UK: University of Oxford.Google Scholar
Malhi, Y., Aragão, L. E. O. C., Metcalfe, D. B., et al. (2009). Comprehensive assessment of carbon productivity, allocation and storage in three Amazonian forests. Global Change Biology 15: 1255–1274.CrossRefGoogle Scholar
Medina, E., Cuevas, E., and Weaver, P. L. (1981). Composición foliar y transpiración de especies lenosas de Pico del Este, Sierra de Luquillo, Puerto Rico. Acta Científica Venezolana 32: 159–165.Google Scholar
Mildenberger, K., Beiderwieden, E., Hsia, Y. J., and Klemm, O. (2009). CO2 and water vapor fluxes above a subtropical mountain cloud forest: the effect of light conditions and fog. Agricultural and Forest Meteorology, doi:10.1016/j.agrformet.2009.06.004CrossRef
Millward, D., Marriner, G. F., and Saunders, A. D. (1984). Cretaceous tholeiitic volcanic rocks form the western Cordillera of Colombia. Journal of the Geological Society 141: 847–860.CrossRefGoogle Scholar
Miyazawa, M., Pavan, M. A., Muraoka, T., Carmo, C. A. F. S., and Mello, W. J. (1999). Análise química de tecidos vegetais. In Manual de análise química de solos, plantas e fertilizantes, ed. Silva, F. C., pp. 172–223. Brasília, Brasil: EMBRAPA.Google Scholar
Moser, G., Hertel, D., and Leuschner, Ch. (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
Murphy, J., and Riley, J. P. (1965). A modified single solution method for estimation of phosphate in natural maters, Analitica Chimica Acta 27: 3–36.Google Scholar
Poorter, H. (1994). Construction costs of biomass: a whole plant perspective. In A Whole-Plant Perspective on Carbon–Nitrogen Interactions, eds. Roy, J. and Garnier, E., pp. 111–127. The Hague: SPB Academic Publishing.Google Scholar
Poorter, H., and Evans, J. R. (1998). Photosynthetic nitrogen-use efficiency of species that differ inherently in specific leaf area. Oecologia 116: 26–37.CrossRefGoogle ScholarPubMed
Poorter, H., and Remkes, C. (1990). Leaf area ratio and net assimilation rate of 24 wild species differing in relative growth rate. Oecologia 83: 553–559.CrossRefGoogle ScholarPubMed
Prince, S. D., Justice, C. O., and Moore, B. III (1994). Monitoring and Modeling of Terrestrial Net and Gross Primary Production, IGBP-DIS Working Paper No. 8. College Park, MD: University of Maryland.Google Scholar
Reich, P. B., Uhl, C., Walters, M. B., and Ellsworth, D. S. (1991). Leaf life-span as a determinant of leaf structure and function among 23 Amazonian tree species. Oecologia 86: 16–24.CrossRefGoogle Scholar
Reich, P. B., Ellsworth, D. S., Walters, M. B., et al. (1999). Generality of leaf trait relationships: a test across six biomes. Ecology 80: 1955–1969.CrossRefGoogle Scholar
Reinhardt, K., and Smith, W. K. (2008). Impacts of cloud immersion on microclimate, photosynthesis and water relations of Abies fraseri Pursh. Poiret in a temperate mountain cloud forest. Oecologia 158: 229–238.CrossRefGoogle Scholar
Rincón-Romero, M. E. (2000). Modelling hydrological sensitivity to land-use change in tropical mountainous environments. Ph.D. thesis, King's College, University of London, London, UK.Google Scholar
Roderick, M. L., Farquhar, G. D., Berry, S., and Noble, I. R. (2001). On the direct effect of clouds and atmospheric particles on the productivity and structure of vegetation. Oecologia 129: 21–30CrossRefGoogle ScholarPubMed
Schawe, M., Glatzel, S., and Gerold, G. (2007). Soil development along an altitudinal transect in a Bolivian tropical montane rainforest: podzolization vs. hydromorphy. Catena 69: 83–90.CrossRefGoogle Scholar
Sentelhas, P. C., Gillespie, T. J., and Santos, E. A. (2007). Leaf wetness duration measurement: comparison of cylindrical and flat plate sensors under different field conditions. International Journal of Biometeorology 51: 265–273.CrossRefGoogle ScholarPubMed
Shipley, B., Lechowicz, M. J., Wright, I., and Reich, P. B. (2006). Fundamental trade-offs generating the worldwide leaf economics spectrum. Ecology 87: 535–541.CrossRefGoogle ScholarPubMed
Shorrocks, V. M. (1997). The occurrence and correction of boron deficiency. Plant and Soil 193: 121–148.CrossRefGoogle Scholar
Smith, W. K., and McClean, T. M. (1989). Adaptive relationship between leaf water repellency, stomatal distribution and gas exchange. American Journal of Botany 76: 465–469.CrossRefGoogle Scholar
Soethe, N., Wilcke, W., Homeier, J., Lehmann, J., and Engels, C. (2008). 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., 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
Thomas, S. C., and Bazzaz, F. A. (1999). Asymptotic height as a predictor of photosynthetic characteristics in Malaysian rain forest trees. Ecology 80: 1607–1622.CrossRefGoogle Scholar
Thornley, J. H. M., and Johnson, I. R. (1990). Plant and Crop Modelling: A Mathematical Approach to Plant and Crop Physiology. Oxford, UK:Oxford University Press.Google Scholar
Valladares, F., Wright, S. J., Lasso, E., Kitajima, K., and Pearcy, R. W. (2000). Plastic phenotypic response to light of 16 congeneric shrubs from a Panamanian rainforest. Ecology 81: 1925–1936.CrossRefGoogle Scholar
Vázquez, J. A., and Givnish, T. J. (1998). Altitudinal gradients in tropical forest composition, structure and diversity in the Sierra de Manantlan. Journal of Ecology 86: 999–1020.Google Scholar
Velázquez-Rosas, N., Meave, J., and Vázquez-Santana, S. (2002). Elevational variation of leaf traits in montane rain forest tree species at La Chinantla, southern Mexico. Biotropica 34: 534–546.CrossRefGoogle Scholar
Vitousek, P. M., and Sanford, R. L. (1986). Nutrient cycling in moist tropical forest. Annual Review of Ecology and Systematics 17: 137–167.CrossRefGoogle Scholar
Waide, R. B., Zimmerman, J. K., and Scatena, F. N. (1998). Controls of primary productivity: lessons from the Luquillo Mountains in Puerto Rico. Ecology 79: 31–37.CrossRefGoogle Scholar
Weaver, P. L., and Murphy, P. G. (1990). Structure and productivity in Puerto Rico's Luquillo Mountains. Biotropica 22: 69–82.CrossRefGoogle Scholar
Wilcke, W., Yasin, S., Valarezo, C., and Zech, W. (2001). Change in water quality during the passage through a tropical montane rain forest in Ecuador. Biogeochemistry 55: 45–72.CrossRefGoogle Scholar
Williams, K., Field, C. B., and Mooney, H. A. (1989). Relationships among leaf construction cost, leaf longevity and light environment in rain forest plants of the genus Piper. American Naturalist 133: 198–211.CrossRefGoogle Scholar
Wright, I. J., Reich, P. B., Westoby, W., et al. (2004). The worldwide leaf economics spectrum. Nature 428: 821–827.CrossRefGoogle ScholarPubMed

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