MAXIMUM CARBOXYLATION VELOCITY OF RUBISCO AND MAXIMUM RATE OF ELECTRON TRANSPORT IN SAPLINGS IN RESPONSE TO VARIATIONS IN ENVIRONMENTAL FACTORS IN CENTRAL AMAZONIA
DOI:
https://doi.org/10.5902/1980509828666Keywords:
nonstomatal limitations, colimitation of photosynthesis, diurnal variation.Abstract
Light availability is one of the main factors that limits photosynthetic rates in saplings in the forest understory. The aims of this study were to determine how photosynthetic parameters (maximum carboxylation velocity of Rubisco – Vc-max and maximum rate of electron transport – Jmax) respond to irradiance, temperature and diurnal variations in the physical environment. Gas exchange data were collected between 08h00 and 16h00, and from September to November (2010) under ambient conditions, temperature of 27± 2 ºC and relative humidity of 70 ± 3%. CO2 saturated photosynthesis (Apot) was measured under light saturation and [CO2] of 2000 μmol mol-1. Data were subjected to analysis of variance and then the Tukey test was used for mean separations. Vc-max and Jmax correlated with photosynthetic rates at [CO2] of 380 μmol mol-1 (A380)and Apot. The increase in intercellular CO2 concentration (Ci) led to increase in photosynthetic rates, up to the point of photosynthesis limitation by the electron transport rate. Below the mutual limitation point (300-569 μmol mol-1) photosynthetic rates were limited by Vc-max. Increases in irradiance and temperature in the forest understory led to increasing the values of A380, Apot, Vc-max and Jmax. However, the effect of time of day on Vc-max and Jmax was not significant (p > 0.05). Absence of an effect of time of day on Vc-max and Jmax is important for the leaf to efficiently use the sun flecks that occasionally puncture the forest floor.
Downloads
References
ALARCÓN, J. G. S. Levantamento florístico e etnobotânico em um hectare de floresta de terra firme na região do Médio Rio Negro, Roraima, Brasil. 2005. 111 f. Dissertação (Mestrado) - Instituto de Pesquisas Jardim Botânico do Rio de Janeiro, Rio de Janeiro, 2005.
ANDRADE, S. O. et al. Inflammatory action and toxicity of Guarea trichilioides L. in rats. Toxicology and Applied Pharmacology, New Mexico, v. 38, p. 39-46, 1976.
BOARDMAN, N. K. Comparative photosynthesis of sun and shade plants. Annual Review of Plant Physiology, Palo Alto, v. 28, p. 355-377, 1977.
CAMACHO, M. D. R. et al. Terpenoids from Guarea rhophalocarpa. Phytochemistry, London, v. 56, p. 203-210, 2001.
CHATROU, L. W.; HE, P. Studies in Annonaceae XXXIII. A revision of Fusaea (Baill.) Saff. Brittonia, New York, v. 52, p. 181-203, 1999.
ELLSWORTH, D. et al. Photosynthesis, carboxylation and leaf nitrogen responses of 16 species to elevated CO2 across four free-air CO2 enrichment experiments in forest, grassland and desert. Global Change Biology, Champaign, v. 10, p. 2121-2138, 2004.
EVANS, J. R. Nitrogen and photosynthesis in the flag leaf of wheat (Triticum aestivum L.). Plant Physiology, United Kingdom, v. 72, p. 297-302, 1983.
EVANS, J. R.; TERASHIMA, I. Photosynthetic characteristics of spinach leaves grown with different nitrogen treatment. Plant Cell Physiology, United Kingdom, v. 29, p. 157-165, 1988.
FARQUHAR, G. D.; VON CAEMMERER, S.; BERRY, J. A. A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta, Berlin, v. 149, p. 78-90, 1980.
FECHINE, I. M. et al. Alkaloids and volatile constituents from Duguetia flagellaris. Biochemical Systematics and Ecology, Oxford, v. 30, p. 267-269, 2002.
FETCHER, N.; OBERBAUER, S. F.; CHAZDON, R. L. Physiological ecology of plants. In: MCDADE, L. A. et al. (Eds.). La Selva: ecology and natural history of a neotropical rain forest. Chicago: The University of Chicago Press, 1994. p. 128-141.
HRSTKA, M. et al. Diurnal regulation of ribulose-1,5-bisphosphate carboxylase/oxygenase activity and its content in Norway spruce needles. Photosynthetica, Praha, v. 45, p. 334-339, 2007.
JADÁN, O. et al. Riqueza y potencial maderable em sistemas agroforestales tradicionales como alternativa al uso del bosque nativo, Amazonia del Ecuador. Revista Forestal Mesoamericana Kurú, Cartago, v. 12, p. 13-22, 2015.
LIMA FILHO, D. A. et al. Aspectos florísticos de 13 hectares da área de Cachoeira Porteira-PA. Acta Amazonica, Manaus, v. 34, p. 415-423, 2004.
LLOYD, J.; FARQUHAR, G. D. Effects of rising temperatures and [CO2] on the physiology of tropical forest trees. Philosophical Transactions of the Royal Society of Biological Sciences, London, v. 363, p. 1811-1817, 2008.
LOPEZ-TOLEDO, L. et al. Soil and light effects on the sapling performance of the shade-tolerant species Brosimum alicastrum (Moraceae) in a Mexican tropical rain forest. Journal of Tropical Ecology, Cambridge, v. 24, p. 629-637, 2008.
MALHI, Y.; WRIGHT, J. Spatial patterns and recent trends in the climate of tropical rainforest regions. Philosophical Transactions of the Royal Society of London, London, v. 359, p. 311-329, 2004.
MANTER, D. K.; KERRIGAN, J. A/Ci curve analysis across a range of woody plant species: influence of regression analysis parameters and mesophyll conductance. Journal of Experimental Botany, United Kingdom, v. 55, p. 2581-2588, 2004.
MARENCO, R. A. et al. Fisiologia de espécies florestais da Amazônia: fotossíntese, respiração e relações hídricas. Revista Ceres, Viçosa, MG, v. 61, p. 786-799, 2014.
MARENCO, R. A. et al. Juvenile tree growth correlates with photosynthesis and leaf phosphorus content in central Amazonia. Revista Ceres, Viçosa, MG, v. 62, p. 175-183, 2015.
MARENCO, R. A.; GONÇALVES, J. F. C.; VIEIRA, G. Leaf gas exchange and carbohydrates in tropical trees differing in successional status in two light environments in central Amazonia. Tree Physiology, Oxford, v. 21, p. 1311-1318, 2001.
MARENCO, R. A.; NASCIMENTO, H. C. S.; MAGALHÃES, N. S. Stomatal conductance in Amazonian tree saplings in response to variations in the physical environment. Photosynthetica, Praha, v. 52, p. 493-500, 2014.
MARTINS, R. C. C. et al. Constituents of the essential oil of Eugenia nitida Camb. (Myrtaceae). Journal of Essential Oil Research, Carol Stream, v. 11, p. 724-726, 1999.
MEDLYN, B. E. et al. Effects of elevated [CO2] on photosynthesis in European forest species: a meta-analysis of model parameters. Plant Cell and Environment, New York, v. 22, p. 1475-1495, 1999.
MENDES, K. R.; MARENCO, R. A. Leaf traits and gas exchange in saplings of native tree species in the Central Amazon. Scientia Agricola, Piracicaba, v. 67, p. 624-632, 2010.
MENDES, K. R.; MARENCO, R. A. Is stomatal conductance of Central Amazonian saplingsinfluenced by circadian rhythms under natural conditions? Theoretical and Experimental Plant Physiology, Campos dos Goytacazes, v. 26, p. 115-125, 2014.
MENDES, K. R.; MARENCO, R. A. Photosynthetic traits of tree species in response to leaf nutrient content in the central Amazon. Theoretical and Experimental Plant Physiology, Campos dos Goytacazes, v. 27, p. 51-59, 2015.
MILLER, R. P.; WANDELLI, E. V.; GRENAND, P. Conhecimento e utilização da floresta pelos índios waimiri-atroari do rio camanau – Amazonas. Acta Botanica Brasílica, Porto Alegre, v. 3, p. 47-56, 1989.
NASCIMENTO, H. C. S.; MARENCO, R. A. Mesophyll conductance variations in response to diurnal environmental factors in Myrcia paivae and Minquartia guianensis in Central Amazonia. Photosynthetica, Praha, v. 51, p. 457-464, 2013.
ONODA, Y.; HIKOSAKA, K.; HIROSE, T. Seasonal change in the balance between capacities of RuBP carboxylation and RuBP regeneration affects CO2 response of photosynthesis in Polygonum cuspidatum. Journal of Experimental Botany, United Kingdom, v. 56, p. 755-763, 2005.
PARRY, M. A. J. et al. Water stress and the diurnal activity of ribulose-1, 5-bisphosphate carboxylase in field grown Nicotiana tabacum genotypes selected for survival at low CO2 concentrations. Plant Physiology and Biochemistry, Paris, v. 31, p. 113-120, 1993.
PONS, T. L.; WELSCHEN, R. A. M. Midday depression of net photosynthesis in the tropical rainforest tree Eperua grandiflora: contributions of stomatal and internal conductances, respiration and Rubisco functioning. Tree Physiology, United Kingdom, v. 23, p. 937-947, 2003.
RESQUE, O. R. Vocabulário de frutas comestíveis na Amazônia. Belém: Museu Paraense Emílio Goeld, 2007. 99 p.
RODRIGUES, P. A. Avaliação de extratos vegetais bioativos de plantas amazônicas sobre a concentração de testosterona sérica em camundongos pós púberes. 2013. 77 f. Dissertação (Mestrado) - Universidade Paulista, São Paulo, 2013.
SELLERS, P. J. et al. Modeling the exchanges of energy, water, and carbon between continents and the atmosphere. Science, Washington, v. 275, p. 502-509, 1997.
TAVARES, J. F. et al. Alkaloids and volatile constituents from the stem of Fusaea longifolia (Aubl.) Saff. (Annonaceae). Brazilian Journal of Pharmacognosy, Curitiba, v. 15, p. 115-118, 2005.
VALLADARES, F. et al. The greater seedling high-light tolerance of Quercus robur over Fagus sylvatica is linked to a greater physiological plasticity. Trees Structure and Function, Berlin, v. 16, p. 395-403, 2002.
VALLADARES, F.; NIINEMETS, Ü. Shade tolerance, a key plant feature of complex nature and consequences. Annual Review of Ecology Evolution and Systematics, Palo Alto, v. 39, p. 237-257, 2008.
WARREN, C. R. Soil water deficits decrease the internal conductance to CO2 transfer but atmospheric water deficits do not. Journal of Experimental Botany, United Kingdom, v. 59, p. 327-334, 2008.
WARREN, C. R.; DREYE, E. Temperature response of photosynthesis and internal conductance to CO2: results from two independent approaches. Journal of Experimental Botany, United Kingdom, v. 57, p. 3057-3067, 2006.
WAY, D. A.; OREN, R. Differential responses to changes in growth temperature between trees from different functional groups and biomes: a review and synthesis of data. Tree Physiology, United Kingdom, v. 30, p. 669-688, 2010.
WULLSCHLEGER, S. D. Biochemical limitations to carbon assimilation in C3 plants – a retrospective analysis of the A/Ci curves from 109 species. Journal of Experimental Botany, United Kingdom, v. 44, p. 907-920, 1993.