Fluorescence, reflectance, and physiological response to water stress in Gmelina arborea Roxb seedlings

Authors

DOI:

https://doi.org/10.15359/ru.35-1.20

Keywords:

Forest physiology, water stress, Gmelina arborea, physiological degradation

Abstract

Fluorescence, reflectance, and physiological response to water stress were analyzed in Gmelina arborea Roxb seedlings. The experiment was conducted for 31 days with two treatments: control plants (a normal water regime was applied) and plants under water stress conditions (water was completely limited for these plants during the extent of the experiment). For both treatments, G. arborea clones were used and evaluated every seven days until the end of the experiment.  Photosynthesis, stomatal conductance, leaf turgor, relative chlorophyll content, fluorescence, and reflectance were analyzed. Results showed that the biomass in plants under stress was reduced by 26.9%, being the leaf coverage the one with the greatest affectation (29.1% decrease), while photosynthesis was reduced by 60.1% (5.8 µmol m-2 s-1) compared to the control plant (14.6 µmol m-2 s-1). For the variables stomatal conductance, turgor, and relative chlorophyll content, the behavior was to decrease values from 20 to 60% as the stress period increased. With respect to fluorescence, two standards were determined: from 400 to 550 nm, fluorescence increased in stressed plants, while from 600 to 725 nm, control plants showed the highest excitation. In both ranges, maximum values were presented at the points corresponding to chlorophyll a and b. Finally, reflectance showed differences between 460 and 770 nm, being the plants under stress conditions the ones showing the highest reflectance. The physiological degradation pattern obtained in the stressed plants is due to the organism’s water loss resulting in stomatal closure, increased production of abscisic acid, decreased cell wall synthesis, and limitations in protein synthesis.

References

Adekunle, V., Alo, A. A., & Adekayode, F. O. (2011). Yields and nutrient pools in soils cultivated with Tectona grandis and Gmelina arborea in Nigerian rainforest ecosystem. Journal of the Saudi Society of Agricultural Sciences, 10(2), 127–135. https://doi.org/10.1016/j.jssas.2011.05.001

Agam, N., Cohen, Y., Berni, J., Alchanatis, V., Kool, D., Dag, A., Yermiyahu, U., & Ben-Gal, A. (2013). An insight to the performance of crop water stress index for olive trees. Agricultural Water Management, 118, 79–86. https://doi.org/10.1016/j.agwat.2012.12.004

Bader, B., Aissaoui, F., Kmicha, I., Salem, A., Chehab, H., Gargouri, K., Boujnah, D., & Chaieb, M. (2015). Effects of salinity stress on water desalination, olive tree (Olea europaea L. cvs “Picholine”, “Meski” and ’Ascolana’) growth and ion accumulation. Desalination, 364, 46–52. https://doi.org/10.1016/j.desal.2015.01.002

Beyer, R., Letort, V., & Cournède, P. H. (2014). Modeling tree crown dynamics with 3D partial differential equations. Frontiers in Plant Science, 5, 1–8. https://doi.org/10.3389/fpls.2014.00329

Boogar, A. R., & Salehi, H. (2020). Developmental indices of cones collected from male plants of Juniperus polycarpos K. Koch under in vitro water deficit and salt stress conditions. South African Journal of Botany, 131, 277–282. https://doi.org/10.1016/j.sajb.2020.02.032

Chen, X., Zhao, P., Ouyang, L., Zhu, L., Ni, G., & Schäfer, K. V. R. (2020). Whole-plant water hydraulic integrity to predict drought-induced Eucalyptus urophylla mortality under drought stress. Forest Ecology and Management, 468. https://doi.org/10.1016/j.foreco.2020.118179

De la Rosa, J. M., Domingo, R., Gómez-Montiel, J., & Pérez-Pastor, A. (2015). Implementing deficit irrigation scheduling through plant water stress indicators in early nectarine trees. Agricultural Water Management, 152, 207–216. https://doi.org/10.1016/j.agwat.2015.01.018

Dell’Amico, J., Moriana, A., Corell, M., Girón, I., Morales, D., Torrecillas, A., & Moreno, F. (2012). Low water stress conditions in table olive trees (Olea europaea L.) during pit hardening produced a different response of fruit and leaf water relations. Agricultural Water Management, 114, 11–17. https://doi.org/10.1016/j.agwat.2012.06.004

Di Vaio, C., Marallo, N., Marino, G., & Caruso, T. (2013). Effect of water stress on dry matter accumulation and partitioning in pot-grown olive trees (cv Leccino and Racioppella). Scientia Horticulturae, 164, 172–177. https://doi.org/10.1016/j.scienta.2013.09.008

Díaz-Barradas, M. C., Gallego-Fernández, J. B.; & Zunzunegui, M. (2020). Plant response to water stress of native and non-native Oenothera drummondii populations. Plant Physiology and Biochemistry, 154, 219–228. https://doi.org/10.1016/j.plaphy.2020.06.001

Eby, W. M., Oyamakin, S. O.; & Chukwu, A. U. (2017). A new nonlinear model applied to the height-DBH relationship in Gmelina arborea. Forest Ecology and Management, 397, 139–149. https://doi.org/10.1016/j.foreco.2017.04.015

Farooq, M., Wahid, A., Kobayashi, N., Fujita, D., & Basra, S. M. A. (2009). Plant drought stress: Effects, mechanisms and management. Sustainable Agriculture, 153–188. https://doi.org/10.1007/978-90-481-2666-8_12

Fournier, C., & Andrieu, B. (1998). A 3D architectural and process-based model of maize development. Annals of Botany, 81(2), 233–250. https://doi.org/10.1006/anbo.1997.0549

Gautier, H., Měch, R., Prusinkiewicz, P., & Varlet-Grancher, C. (2000). 3D architectural modelling of aerial photomorphogenesis in white clover (Trifolium repens L.) using L-systems. Annals of Botany, 85(3), 359–370. https://doi.org/10.1006/anbo.1999.1069

Holst, T., Hauser, S., Kirchgäßner, A., Matzarakis, A., Mayer, H., & Schindler, D. (2004). Measuring and modelling plant area index in beech stands. International Journal of Biometeorology, 48(4), 192–201. https://doi.org/10.1007/s00484-004-0201-y

Hsiao, T. C. (1931). Plant responses to sawdust. Proceedings of the Indiana Academy of Science, 41, 125–126.

Huzsvai, L., & Rajkai, K. (2009). Modeling of plant adaptation to climatic drought induced water deficit. Biologia, 64(3), 536–540. https://doi.org/10.2478/s11756-009-0092-9

Jiménez, E., Vega, J. A., Pérez-Gorostiaga, P., Fonturbel, T., & Fernández, C. (2010). Evaluation of sap flow density of acacia melanoxylon R. Br. (blackwood) trees in overstocked stands in north-western Iberian Peninsula. European Journal of Forest Research, 129(1), 61–72. https://doi.org/10.1007/s10342-008-0252-4

Kaya, C., Ashraf, M., Wijaya, L., & Ahmad, P. (2019). The putative role of endogenous nitric oxide in brassinosteroid-induced antioxidant defence system in pepper (Capsicum annuum L.) plants under water stress. Plant Physiology and Biochemistry, 143, 119–128. https://doi.org/10.1016/j.plaphy.2019.08.024

Li, W., Jiang, Y., Dong, M., Du, E., Zhou, Z., Zhao, S., & Xu, H. (2020). Diverse responses of radial growth to climate across the southern part of the Asian boreal forests in northeast China. Forest Ecology and Management, 458(19). https://doi.org/10.1016/j.foreco.2019.117759

Ma, H., Song, J., Wang, J., Xiao, Z., & Fu, Z. (2014). Improvement of spatially continuous forest LAI retrieval by integration of discrete airborne LiDAR and remote sensing multi-angle optical data. Agricultural and Forest Meteorology, 189–190, 60–70. https://doi.org/10.1016/j.agrformet.2014.01.009

Maatallah, S., Ghanem, M. E., Albouchi, A., Bizid, E., & Lutts, S. (2010). A greenhouse investigation of responses to different water stress regimes of Laurus nobilis trees from two climatic regions. Journal of Arid Environments, 74(3), 327–337. https://doi.org/10.1016/j.jaridenv.2009.09.008

Marín-Ortiz, J. C., Gutiérrez-Toro, N., Botero-Fernández, V., & Hoyos-Carvajal, L. M. (2020). Linking physiological parameters with visible/near-infrared leaf reflectance in the incubation period of vascular wilt disease. Saudi Journal of Biological Sciences, 27(1), 88–99. https://doi.org/10.1016/j.sjbs.2019.05.007

Miyazawa, Y., Tateishi, M., Komatsu, H., Iwanaga, F., Mizoue, N., Ma, V., Sokh, H., & Kumagai, T. (2014). Implications of leaf-scale physiology for whole tree transpiration under seasonal flooding and drought in central Cambodia. Agricultural and Forest Meteorology, 198, 221–231. https://doi.org/10.1016/j.agrformet.2014.08.013

Moreno, L. (2009). Respuesta de las plantas al estrés por déficit hídrico . Una revisión Plant responses to water deficit stress . A review. Agronomía Colombiana, 27(2), 179–191.

Moya, R., Rodríguez-Zúñiga, A., & Puente-Urbina, A. (2017). Thermogravimetric and devolatilisation analysis for five plantation species: Effect of extractives, ash compositions, chemical compositions and energy parameters. Thermochimica Acta, 647, 36–46. https://doi.org/10.1016/j.tca.2016.11.014

Naumann, J. C., Young, D. R., & Anderson, J. E. (2008). Leaf chlorophyll fluorescence, reflectance, and physiological response to freshwater and saltwater flooding in the evergreen shrub, Myrica cerifera. Environmental and Experimental Botany, 63(1–3), 402–409. https://doi.org/10.1016/j.envexpbot.2007.12.008

Ortuño, M. F., García-Orellana, Y., Conejero, W., Ruiz-Sánchez, M. C., Alarcón, J. J., & Torrecillas, A. (2006). Stem and leaf water potentials, gas exchange, sap flow, and trunk diameter fluctuations for detecting water stress in lemon trees. Trees - Structure and Function, 20(1), 1–8. https://doi.org/10.1007/s00468-005-0004-8

Paulus, S., Schumann, H., Kuhlmann, H., & Léon, J. (2014). High-precision laser scanning system for capturing 3D plant architecture and analysing growth ofcereal plants. Biosystems Engineering, 121, 1–11. https://doi.org/10.1016/j.biosystemseng.2014.01.010

Pollastrini, M., Desotgiu, R., Cascio, C., Bussotti, F., Cherubini, P., Saurer, M., Gerosa, G., & Marzuoli, R. (2010). Growth and physiological responses to ozone and mild drought stress of tree species with different ecological requirements. Trees - Structure and Function, 24(4), 695–704. https://doi.org/10.1007/s00468-010-0439-4

Rojas, A., Moreno, L., Melgarejo, L., & Rodríguez, M. (2012). Physiological response of gmelina (Gmelina arborea Roxb.) to hydric conditions of the colombian Caribbean. Agronomía Colombiana, 30, 52-58.

Sánchez-Costa, E., Poyatos, R., & Sabaté, S. (2015). Contrasting growth and water use strategies in four co-occurring Mediterranean tree species revealed by concurrent measurements of sap flow and stem diameter variations. Agricultural and Forest Meteorology, 207, 24–37. https://doi.org/10.1016/j.agrformet.2015.03.012

Sonobe, R., Sano, T., & Horie, H. (2018). Using spectral reflectance to estimate leaf chlorophyll content of tea with shading treatments. Biosystems Engineering, 175, 168–182. https://doi.org/10.1016/j.biosystemseng.2018.09.018

Tenorio, C., Moya, R., Arias-Aguilar, D., & Briceño-Elizondo, E. (2016). Biomass yield and energy potential of short-rotation energy plantations of Gmelina arborea one year old in Costa Rica. Industrial Crops and Products, 82, 63–73. https://doi.org/10.1016/j.indcrop.2015.12.005

Valverde, J. C., & Arias, D. (2020). Efectos del estrés hídrico en crecimiento y desarrollo fisiológico de Gliricidia sepium (Jacq.) Kunth ex Walp. Colombia Forestal, 23(1), 29-53. https://doi.org/10.14483/2256201X.14786

Varone, L., Ribas-Carbo, M., Cardona, C., Gallé, A., Medrano, H., Gratani, L., & Flexas, J. (2012). Stomatal and non-stomatal limitations to photosynthesis in seedlings and saplings of Mediterranean species pre-conditioned and aged in nurseries: Different response to water stress. Environmental and Experimental Botany, 75, 235–247. https://doi.org/10.1016/j.envexpbot.2011.07.007

Vilfan, N., Vander Tol, C., Muller, O., Rascher, U., & Verhoef, W. (2016). Fluspect-B: A model for leaf fluorescence, reflectance and transmittance spectra. Remote Sensing of Environment, 186, 596–615. https://doi.org/10.1016/j.rse.2016.09.017

Wakamori, K., Mizuno, R., Nakanishi, G., & Mineno, H. (2020). Multimodal neural network with clustering-based drop for estimating plant water stress. Computers and Electronics in Agriculture, 168, 105118. https://doi.org/10.1016/j.compag.2019.105118

Zhu, L. W., Zhao, P., Wang, Q., Ni, G. Y., Niu, J. F., Zhao, X. H., Zhang, Z. Z., Zhao, P. Q., Gao, J. G., Huang, Y. Q., Gu, D. X., & Zhang, Z. F. (2015). Stomatal and hydraulic conductance and water use in a eucalypt plantation in Guangxi, southern China. Agricultural and Forest Meteorology, 202, 61–68. https://doi.org/10.1016/j.agrformet.2014.12.003

Published

2021-01-31

Issue

Section

Original scientific papers (evaluated by academic peers)

Comentarios (ver términos de uso)

Most read articles by the same author(s)