How does Cariniana estrellensis respond to different irradiance levels?

Flávia Carolina Santos Portela, Bernardo Pretti Becacici Macieira, Leonardo Valandro Zanetti, Vinícius Novo Gama, Diolina Moura Silva, Camilla Rozindo Dias Milanez, Geraldo Rogério Faustini Cuzzuol

Journal of Forestry Research ›› 2019, Vol. 30 ›› Issue (1) : 31-44.

Journal of Forestry Research All Journals
Journal of Forestry Research ›› 2019, Vol. 30 ›› Issue (1) : 31-44. DOI: 10.1007/s11676-017-0578-1
Original Paper

How does Cariniana estrellensis respond to different irradiance levels?

Author information +
History +

Abstract

Based on reports that variables related to photosynthesis (net assimilatory ratio and chloroplast pigments) are more plastic than the morphological and biochemical variables in a climax tropical species, Cariniana estrellensis, under contrasting irradiance, we hypothesised that plasticity of gas exchange variables is higher in relation to growth, biochemical and anatomical variables. Plants that were 14 months old were subjected to 200 up to 2000 µmol m−2 s−1 of photo synthetically active radiation (PAR) for 140 days. Growth increased up to 1400 µmol m−2 s−1 PAR and then decreased at 2000 µmol m−2 s−1 PAR (full sunlight). This was related to the rate of photosynthesis (A) which showed the same tendency as photosystem II performance index (PIABS). The greater thickness of the secondary xylem at 1400 µmol m−2 s−1 PAR indicated a higher water conductance capacity. The decrease in specific leaf area, elongation of mesophyll cells, and increase in stomatal density observed at higher irradiances were associated with higher leaf fructose and sucrose concentrations. We concluded that the better growth in partial shade was due to higher photosynthetic capacity. On the other hand, photosynthesis was inhibited equally in full sun and deep shade. The high adjustment capacity of C. estrellensis to wide amplitudes of irradiance was provided by greater plasticity of gas exchange variables in relation to growth, anatomical, and biochemical variables.

Keywords

Anatomy / Ecophysiology / Gas exchange / Phenotypic plasticity / Soluble carbohydrates

Cite this article

Download citation ▾
Flávia Carolina Santos Portela, Bernardo Pretti Becacici Macieira, Leonardo Valandro Zanetti, Vinícius Novo Gama, Diolina Moura Silva, Camilla Rozindo Dias Milanez, Geraldo Rogério Faustini Cuzzuol. How does Cariniana estrellensis respond to different irradiance levels?. Journal of Forestry Research, 2019, 30(1): 31‒44 https://doi.org/10.1007/s11676-017-0578-1
This is a preview of subscription content, contact us for subscripton.

References

Barros FV, Goulart MF, Telles SBS, Lovato MB, Valladares F, Lemos-Filho JP. Phenotypic plasticity to light of two congeneric trees from contrasting habitats: brazilian Atlantic forest versus cerrado (savanna). Plant Biol, 2012, 14: 208-215.
Budowski G. Distribution of tropical American rain forest species in the light of successional processes. Turrialba, 1965, 15: 40-42.
Bukatsch F. Bemerkungen zur doppelfärbung astrablau-safranin. Mikrokosmos, 1972, 61: 255.
Dias DP, Marenco R. Fotossíntese e fotoinibição em mogno e acariquara em função da luminosidade e temperatura foliar. Pesqui Agropecu Bras, 2007, 42(3): 305-311.
CrossRef Google scholar
Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith F. Colorimetric method for determination of sugars and related substances. Anal Chem, 1956, 28: 350-356.
CrossRef Google scholar
Engel VL (2001) Estudo fenológico de espécies arbóreas de uma floresta tropical em Linhares, In: ES (Ph.D. Thesis). Universidade Estadual de Campinas, São Paulo
Franklin GL. Preparation of thin sections of synthetic resins and wood-resin composites, and a new macerating method for wood. Nature, 1945, 155: 51.
CrossRef Google scholar
Frigeri RBC (2007) Relação entre raiz e parte aérea de plântulas de espécies arbóreas tropicais sob diferentes níveis de radiação solar (Ph.D. Thesis). Universidade Estadual de Campinas, São Paulo
Gaburro TA, Gama VN, Zanetti L, Milanez CRD, Cuzzuol GRF. Physiological variables related to photosynthesis are more plastic than the morphological and biochemistry in non-pioneer tropical trees under contrasting irradiance. Braz J Bot, 2014, 37(4): 395-402.
Ginzberg I, Barel G, Ophir R, Tzin E, Tanami Z, Muddarangappa T, De Jong W, Fogelman E. Transcriptomic profiling of heat-stress response in potato periderm. J Exp Bot, 2009, 60(15): 4411-4421.
CrossRef Google scholar
Gonçalves JFC, Marenco RA, Vieira G. Concentration of photosynthetic pigments and chlorophyll fluorescence of mahogany and tonka bean under two light environments. Braz J Plant Physiol, 2001, 13: 149-157.
Gonçalves JFC, Barreto DCS, Santos-Júnior UM, Fernandes AV, Sampaio PTB, Buckeridge MS. Growth, photosynthesis and stress indicators in young rosewood plants (Aniba rosaeodora Ducke) under different light intensities. Braz J Plant Physiol, 2005, 17: 325-334.
CrossRef Google scholar
Gonçalves JFC, Santos-Júnior UM, Nina-Júnior AR, Chevreuil LR. Energetic flux and performance index in copaiba (Copaifera multijuga Hayne) and mahogany (Swietenia macrophylla King) seedlings grown under two irradiance environments. Braz J Plant Physiol, 2007, 19: 171-184.
CrossRef Google scholar
Hanba YT, Kogami H, Terashima I. The effect of growth irradiance on leaf anatomy and photosynthesis in Acer species differing in light demand. Plant Cell Environ, 2002, 25: 1021-1030.
CrossRef Google scholar
Jermyn MA. A new method for the determination of ketohexoses in presence of aldohexoses. Nature, 1956, 177: 38-39.
CrossRef Google scholar
Johansen DA. Plant microtechnique, 1940, New York: McGraw-Hill Book Co..
Kitajima K, Hogan KP. Increases of chlorophyll a/b ratios during acclimation of tropical woody seedlings to nitrogen limitation and high light. Plant Cell Environ, 2003, 26: 857-865.
CrossRef Google scholar
Kraus JE, Arduim M. Manual básico de métodos em morfologia vegetal, 1997, Seropédica: Universidade Rural.
Krause GH, Koroleva OY, Dalling JW, Winter K. Acclimation of tropical tree seedlings to excessive light in simulated tree-fall gaps. Plant Cell Environ, 2001, 24: 1345-1352.
CrossRef Google scholar
Laisk A, Eichelmann H, Oja V, Rasulov B, Padu E, Bichele I, Pettai H, Kull O. Adjustment of leaf photosynthesis to shade in a natural canopy: rate parameters. Plant Cell Environ, 2005, 28: 375-388.
CrossRef Google scholar
Lambers H, Poorter H. Inherent variation in growth rate between higher plants: a search for physiological causes and ecological consequences. Adv Ecol Res, 1992, 23: 187-261.
CrossRef Google scholar
Lambers H, Chapim FS III, Pons TL. Plant physiological ecology, 2008 2 Berlin: Springer
CrossRef Google scholar
Law RD, Crafts-Brandner SJ. Inhibition and acclimation of photosynthesis to heat stress is closely correlated with activation of Ribulose-1,5-bisphosphate carboxylase/oxygenase. Plant Physiol, 1999, 120: 173-182.
CrossRef Google scholar
Li XG, Li JY, Zhao JP, Xu PL, He QW. Xanthophyll cycle and inactivation of photosystem II reaction centers alleviating reducing pressure to photosystem I in morning glory leaves under short-term high irradiance. J Integr Plant Biol, 2007, 49: 1047-1053.
CrossRef Google scholar
Lichtenthaler HK, Welburn AR. Determination of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochem Soc Trans, 1983, 11: 591-592.
CrossRef Google scholar
Magalhães NS, Marenco RA, Mendes KR. Aclimatação de mudas de acariquara à alta irradiância. Pesqui Agropecu Bras, 2009, 44(7): 687-694.
CrossRef Google scholar
Marcati CR, Milanez CRD, Machado SR. Seasonal development of secondary xylem and phloem in Schizolobium parahyba (Vell.) Blake (Leguminosae: caesalpinoidae). Trees, 2008, 22: 3-12.
CrossRef Google scholar
Marenco RA, Golçalves JFC, Vieira G. Leaf gas exchange and carbohydrates in tropical trees different in successional status in two light environments in central Amazonia. Tree Physiol, 2001, 21: 1311-1318.
CrossRef Google scholar
Marques AR, Garcia QS, Rezende JLP, Fernandes GW. Variations in leaf characteristics of two species of Miconia in the Brazilian cerrado under different light intensities. Trop Ecol, 2000, 41: 47-60.
Mengarda LHG, Souza RLF, Campostrini E, Reis FO, Vendrame WA, Cuzzuol GRF. Light as an indicator of ecological succession in brazilwood (Caesalpinia echinata Lam.). Braz J Plant Physiol, 2009, 21: 55-64.
CrossRef Google scholar
Mengarda LHG, Milanez CRD, Silva DM, Aguilar MAG, Cuzzuol GRF. Morphological and physiological adjustments of brazilwood (Caesalpinia echinata Lam.) to direct solar radiation. Braz J Plant Physiol, 2012, 24(3): 161-172.
CrossRef Google scholar
Nadeau JA, Sack FD. Somerville CR, Meyerowitz EM. Stomatal development in Arabidopsis. The Arabidopsis Book, 2002, Rockville: American Society of Plant Biologists.
Nishizawa A, Yabuta Y, Shigeoka S. Galactinol and raffinose con-stitute a novel function to protect plants from oxidative damage. Plant Physiol, 2008, 147: 1251-1263.
CrossRef Google scholar
Nunes YRF, Petrere-Júnior M. Structure and dynamics of Cariniana estrellensis (Lecythidaceae) population in a fragment of Atlantic Forest in Minas Gerais, Brazil. Rodriguésia, 2012, 63(2): 257-267.
CrossRef Google scholar
Oguchi R, Hikosaka K, Hirose T. Leaf anatomy as a constraint for photosynthetic acclimation: differential responses in leaf anatomy to increasing growth irradiance among three deciduous trees. Plant Cell Environ, 2005, 28: 916-927.
CrossRef Google scholar
Poorter H, Nagel O. The role of biomass allocation in the growth response of plants to different levels of light, CO2, nutrients and water: a quantitative review. Aust J Plant Physiol, 2000, 27: 595-607.
Riazi A, Matsuda K, Arslan A. Water-stress induced changes in concentrations of proline and other solutes in growing regions of young barley leaves. J Exp Bot, 1985, 36: 1716-1725.
CrossRef Google scholar
Rossato DR, Kolb RM. Gochnatia polymorpha (Less.) Cabrera (Asteraceae) changes in leaf structure due to differences in light and edaphic conditions. Acta Botanica Bras, 2012, 24: 133-149.
Rozendaal DMA, Hurtado VH, Poorter L. Plasticity in leaf traits of 38 tropical tree species in response to light: relationships with demand and adult stature. Funct Ecol, 2006, 20: 207-216.
CrossRef Google scholar
Sass JE. Elements of botanical microtechnique, 1958, New York: McGraw-Hill.
Schuetz M, Smith R, Ellis B. Xylem tissue specification, patterning, and differentiation mechanisms. J Exp Bot, 2013, 64(1): 11-31.
CrossRef Google scholar
Siegert CM, Levia DF. Stomatal conductance and transpiration of co-occurring seedlings with varying shade tolerance. Trees, 2011, 25: 1091-1102.
CrossRef Google scholar
Sielewiesiuk J. Why there are photodamages to photosystem II at low light intensities. Acta Physiol Plant, 2002, 24: 399-406.
CrossRef Google scholar
Silvestrini M, Válio IFM, Mattos EA. Photosynthesis and carbon gain under contrasting light levels in seedlings of a pioneer and a climax tree from a Brazilian semideciduous tropical forest. Braz J Bot, 2007, 30: 463-474.
CrossRef Google scholar
Souza RP, Válio IFM. Seedling growth of fifteen Brazilian tropical tree species differing in sucessional status. Braz J Bot, 2003, 26: 35-47.
Strasser RJ, Srivasta A, Tsimilli-Michael M (2004) Analysis of the fluorescence transient. In: Papageorgiou GC, Govindjee (eds) Chlorophyll fluorescence: a signature of photosynthesis. Advances in Photosynthesis and Respiration Series, vol 19. pp 321–362
Strasser RJ, Tsimilli-Michael M, Qiang S, Goltsev V. Simultaneous in vivo recording of prompt and delayed fluorescence and 820-nm reflection changes during drying and after rehydration of the resurrection plant Haberlea rhodopensis. Biochem Biophys Acta, 2010, 1797: 1313-1326.
Swaine MD, Whitmore TC. On the definition of ecological species groups in tropical rain forests. Vegetatio, 1988, 75: 81-86.
CrossRef Google scholar
Taiz L, Zeiger E. Plant Physiology, 2013 5 Massachusetts: Publishers Sunderland.
Terashima I, Hanba YT, Tazoe Y, Vyas P, Yano S. Irradiance and phenotype: comparative eco-development of sun and shade leaves in relation to photosynthetic CO2 diffusion. J Exp Bot, 2006, 57: 343-354.
CrossRef Google scholar
Valladares F, Niinemets U. Shade tolerance, a key plant feature of complex nature and consequences. Annu Rev Ecol Evol Syst, 2008, 38: 237-257.
CrossRef Google scholar
Valladares F, Wright SJ, Lasso E, Kitajima K, Pearcy RW. Plastic phenotypic response to light of 16 congeneric shrubs from a Panamanian rainforest. Ecology, 2000, 81: 1925-1936.
CrossRef Google scholar
Valladares F, Arrieta S, Aranda I, Lorenzo D, Sanches-Gómez D, Tena D, Suárez F, Pardos PA. Shade tolerance, photoinhibition sensitivity and phenotypic plasticity of Ilex aquifolium in continental Mediterranean sites. Tree Physiol, 2005, 25: 1041-1052.
CrossRef Google scholar
Vieira TO, Lage-Pinto F, Ribeiro DR, Alencar TS, Vitória AP. Light stress in jequitibá-rosa seedlings (Cariniana legalis Lecythidaceae): monitoring photosynthetic acclimation capacity under two light intensities. Vértices, 2011, 13(3): 129-142.
CrossRef Google scholar
Xiang M, Chen S, Wang L, Dong Z, Huang J, Zhang Y, Strasser RJ. Effect of vulculic acid produced by Nimbya alternantherae on the photosynthetic apparatus of Alternanthera philoxeroides. Plant Physiol Biochem, 2013, 65: 81-88.
CrossRef Google scholar
Yusuf MA, Kumar D, Rajwanshi R, Strasser RJ, Tsimilli-Michael M, Govindjee Sarin NB. Overexpression of y-tocopherol methyl transferase gene in Brassica juncea plants alleviates abiotic stress: physiological and chlorophyll a fluorescence measurements. Biochem Biophys Acta, 2010, 1797: 1428-1438.

9

Accesses

22

Citations

Detail

Sections
Recommended

/