Early testing for improving growth under water shortage in Eucalyptus globulus Labill.

Keywords: heterosis, inbreeding depression, native embolism specific leaf area, predawn leaf water potential, stomatal conductance, plasticity

Abstract

Aim of study: We aimed at identifying differences in the response to water shortage between Eucalyptus globulus clones.

Area of study: Field trials were established in SW Spain.

Material and methods: Potted plants from six clones were grown in a greenhouse for 35 days under two watering regimes. Two clones were F0 genotypes and the other four were F1 (hybrid) genotypes, including one inbred clone. Differences in stomatal conductance, hydraulic traits, growth and specific leaf area (SLA) were analyzed.

Main results: Water shortage decreased SLA, growth in height and leaf area and leaf-specific hydraulic conductivity (KLmax). We measured the highest growth in F1 genotypes and the lowest in the clone in which SLA was lowest. The inbred clone showed the highest growth reduction under water shortage. There was substantial hysteresis between leaf water potential (Y) and native embolism, most probably a result of combined cavitation and refilling. High losses of hydraulic conductance were compatible with high stomatal conductances. Maximum values of stomatal conductance decreased with the soil water content estimated from predawn Y and were lowest in the inbred clone, showing less plasticity and a diminished ability to cope with high temperatures, which could explain its poor development under field conditions.

Research highlights: Soil water content and predawn Y appeared as critical factors controlling stomata closure, while stomatal conductance and SLA could be useful to predict differences in growth and survival from early trials.

Downloads

Download data is not yet available.

References

Anderegg WRL, Wolf A, Arango-Velez A, Choat B, Chmura DJ, Jansen S, et al., 2017. Plant water potential improves prediction of empirical stomatal models. PLoS ONE 12: e0185481. https://doi.org/10.1371/journal.pone.0185481

Barotto AJ, Monteoliva S, Gyenge J, Martinez-Meier A, Fernandez ME, 2018. Functional relationships between wood structure and vulnerability to xylem cavitation in races of Eucalyptus globulus differing in wood density. Tree Physiol 38: 243-251. https://doi.org/10.1093/treephys/tpx138

Brodribb TJ, Hill RS, 2000. Increases in water potential gradient reduce xylem conductivity in whole plants. Evidence from a low-pressure conductivity method. Plant Physiol 123: 1021-1028. https://doi.org/10.1104/pp.123.3.1021

Brodribb TJ, Holbrook NM, 2004. Stomatal protection against hydraulic failure: a comparison of coexisting ferns and angiosperms. New Phytol 162: 663-670. https://doi.org/10.1111/j.1469-8137.2004.01060.x

Cañete-Salinas P, Zamudio F, Yáñez M, Gyenge J, Valdés H, Espinosa C et al., 2019. Responses in growth and physiological traits in two Populus × canadensis clones ('I-214' and 'I-488') submitted to different irrigation frequencies in central Chile. For Ecol Manage 449: 117455. https://doi.org/10.1016/j.foreco.2019.117455

Carminati A, Ahmed MA, Zarebanadkouki M, Cai G, Lovric G, Javaux M, 2020, Stomatal closure prevents the drop in soil water potential around roots. New Phytol 226: 1541-1543. https://doi.org/10.1111/nph.16451

Creek D, Lamarque LJ, Torres-Ruiz JM, Parise C, Burlett R, Tissue DT, et al., 2020. Xylem embolism in leaves does not occur with open stomata: evidence from direct observations using the optical visualization technique. J Exp Bot 71: 1151-1159. https://doi.org/10.1093/jxb/erz474

Diémé JS, Armas C, Rusch GM, Pugnaire FI, 2019. Functional responses of four Sahelian tree species to resource availability. Flora 254: 181-187. https://doi.org/10.1016/j.flora.2018.10.009

Espinoza SE, Magni CR, Santelices RE, Ivković M, Cabrera AM, 2016. Changes in drought tolerance of Pinus radiata in Chile associated with provenance and breeding generation. Ann For Sci 73: 267-275. https://doi.org/10.1007/s13595-015-0498-1

Faralli M, Matthews J, Lawson T, 2019. Exploiting natural variation and genetic manipulation of stomatal conductance for crop improvement. Curr Opin Plant Biol 49: 1-7. https://doi.org/10.1016/j.pbi.2019.01.003

Franks PJ, Drake PL, Beerling DJ, 2009. Plasticity in maximum stomatal conductance constrained by negative correlation between stomatal size and density: an analysis using Eucalyptus globulus. Plant Cell Environ 32: 1737-1748. https://doi.org/10.1111/j.1365-3040.2009.002031.x

Hernandez MJ, Montes F, Ruiz F, López G, Pita P, 2016. The effect of vapour pressure deficit on stomatal conductance, sap pH and leaf-specific hydraulic conductance in Eucalyptus globulus clones grown under two watering regimes. Ann Bot 117: 1063-1071. https://doi.org/10.1093/aob/mcw031

Isakov Y, 2021. The effect of a single inbreeding on the growth and development of fast-growing tree species, Betula pendula and Betula pubescens. IOP Conf. Ser.: Earth Environ Sci 875: 012014. https://doi.org/10.1088/1755-1315/875/1/012014

Johnsen K, Major JE, Maier CA, 2003. Selfing results in inbreeding depression of growth but not of gas exchange of surviving adult black spruce trees. Tree Physiol 23: 1005-1008. https://doi.org/10.1093/treephys/23.14.1005

Klein T, 2014. The variability of stomatal sensitivity to leaf water potential across tree species indicates a continuum between isohydric and anisohydric behaviours. Funct Ecol 28: 1313-1320. https://doi.org/10.1111/1365-2435.12289

Knipfer T, Cuneo IF, Brodersen CR, McElrone AJ, 2016. In situ visualization of the dynamics in xylem embolism formation and removal in the absence of root pressure: A study on excised grapevine stems. Plant Physiol 171: 1024-1036. https://doi.org/10.1104/pp.16.00136

Lambers H, Oliveira RS, 2019. Plant physiological ecology, 3rd Ed. Springer, Cham, Switzerland, 736 pp. https://doi.org/10.1007/978-3-030-29639-1

López R, López de Heredia U, Collada C, Cano FJ, Emerson BC, Cochard H, et al., 2013. Vulnerability to cavitation, hydraulic efficiency, growth and survival in an insular pine (Pinus canariensis). Ann Bot 111(6): 1167-1179. https://doi.org/10.1093/aob/mct084

López R, Ramírez-Valiente JA, Pita P, 2022. How plants cope with heatwaves in a drier environment. Flora 295: 152148. https://doi.org/10.1016/j.flora.2022.152148

Lu ZM, Zeiger E, 1994. Selection for higher yields and heat resistance in Pima cotton has caused genetically determined changes in stomatal conductance. Physiol Plantarum 92: 273-278. https://doi.org/10.1034/j.1399-3054.1994.920212.x

Lu ZM, Quiñónez MA, Zeiger E, 2000. Temperature dependence of guard cell respiration and stomatal conductance co-segregate in an F2 population of Pima cotton. Aust J Plant Physiol 27: 457-462. https://doi.org/10.1071/PP98128

Maseda PH, Fernández RJ, 2016. Growth potential limits drought morphological plasticity in seedlings from six Eucalyptus provenances. Tree Physiol 36: 243-251. https://doi.org/10.1093/treephys/tpv137

Mira E, Cochard H, Evette A, Dulormne M, 2023. Growth, xylem vulnerability to cavitation and leaf cell response to dehydration in tree seedlings of the Caribbean dry forest. Forests 14: 697. https://doi.org/10.3390/f14040697

Pammenter NW, Vander Willigen C, 1998. A mathematical and statistical analysis of the curves illustrating vulnerability to cavitation. Tree Physiol 18: 589-593. https://doi.org/10.1093/treephys/18.8-9.589

Polle A, Chen SL, Eckert C, Harfouche A, 2019. Engineering drought resistance in forest trees. Front Plant Sci 9: 1875. https://doi.org/10.3389/fpls.2018.01875

Poorter H, Sack L, 2012. Pitfalls and possibilities in the analysis of biomass allocation patterns in plants. Front Plant Sci 3. https://doi.org/10.3389/fpls.2012.00259

Purcell C, Batke SP, Yiotis C, Caballero R, Soh WK, Murray M, et al., 2018. Increasing stomatal conductance in response to rising atmospheric CO2. Ann Bot 121: 1137-1149. https://doi.org/10.1093/aob/mcx208

Rodríguez ME, Lauff D, Cortizo S, Luquez VMC, 2020. Variability in flooding tolerance, growth and leaf traits in a Populus deltoides intraspecific progeny. Tree Physiol 40: 19-29. https://doi.org/10.1093/treephys/tpz128

Sandner TM, Matthies D, Waller DM, 2021. Stresses affect inbreeding depression in complex ways: disentangling stress-specific genetic effects from effects of initial size in plants. Heredity 127: 347-356. https://doi.org/10.1038/s41437-021-00454-5

Secchi F, Pagliarani C, Zwieniecki MA, 2017. The functional role of xylem parenchyma cells and aquaporins during recovery from severe water stress. Plant Cell Environ 40: 858-871. https://doi.org/10.1111/pce.12831

Sow MD, Le Gac AL, Fichot R, Lanciano S, Delaunay A, Le Jan I, et al., 2021. RNAi suppression of DNA methylation affects the drought stress response and genome integrity in transgenic poplar. New Phytol 232(1): 80-97. https://doi.org/10.1111/nph.17555

Sparks JP, Black RA, 1999. Regulation of water loss in populations of Populus trichocarpa: the role of stomatal control in preventing xylem cavitation. Tree Physiol 19: 453-459. https://doi.org/10.1093/treephys/19.7.453

Sperry JS, Donnelly JR, Tyree MT, 1988. A method for measuring hydraulic conductivity and embolism in xylem. Plant Cell Environ 11: 35-40. https://doi.org/10.1111/j.1365-3040.1988.tb01774.x

Sperry JS, Stiller V, Hacke UG, 2003. Xylem hydraulics and the soil-plant-atmosphere continuum: opportunities and unresolved issues. Agron J 95: 1362-1370. https://doi.org/10.2134/agronj2003.1362

Taylor G, Donnison IS, Murphy-Bokern D, Morgante M, Bogeat-Triboulot MB, Bhalerao R, et al., 2019. Sustainable bioenergy for climate mitigation: developing drought-tolerant trees and grasses. Ann Bot 124: 513-520. https://doi.org/10.1093/aob/mcz146

Tognetti R, Longobucco A, Raschi A, 1998. Vulnerability of xylem to embolism in relation to plant hydraulic resistance in Quercus pubescens and Quercus ilex co-occurring in a Mediterranean coppice stand in central Italy. New Phytol 139: 437-447. https://doi.org/10.1046/j.1469-8137.1998.00207.x

Tomé M, Almeida MH, Barreiro S, Branco MR, Deus E, Pinto G, et al., 2021. Opportunities and challenges of Eucalyptus plantations in Europe: The Iberian Peninsula experience. Eur J Forest Res 140: 489-510. https://doi.org/10.1007/s10342-021-01358-z

Tortosa I, Escalona JM, Opazo I, Douthe C, Medrano H, 2022. Genotype variations in water use efficiency correspond with photosynthetic traits in Tempranillo grapevine clones. Agronomy 12: 1874. https://doi.org/10.3390/agronomy12081874

Vander Willigen C, Pammenter NW, 1998. Relationship between growth and xylem hydraulic characteristics of clones of Eucalyptus spp. at contrasting sites. Tree Physiol 18: 595-600. https://doi.org/10.1093/treephys/18.8-9.595

Vander Willigen C, Sherwin HW, Pammenter NW, 2000. Xylem hydraulic characteristics of subtropical trees from contrasting habitats grown under identical environmental conditions. New Phytol 145: 51-59. https://doi.org/10.1046/j.1469-8137.2000.00549.x

Vilagrosa A, Bellot J, Vallejo VR, Gil-Pelegrín E, 2003. Cavitation, stomatal conductance, and leaf dieback in seedlings of two co-occurring Mediterranean shrubs during an intense drought. J Exp Bot 54: 2015-2024. https://doi.org/10.1093/jxb/erg221

Wang T, Aitken SN, Kavanagh KL, 2003. Selection for improved growth and wood quality in lodgepole pine: effects on phenology, hydraulic architecture and growth of seedlings. Trees 17: 269-277. https://doi.org/10.1007/s00468-002-0236-9

Wikberg J, Ögren E, 2007. Variation in drought resistance, drought acclimation and water conservation in four willow cultivars used for biomass production. Tree Physiol 27: 1339-1346. https://doi.org/10.1093/treephys/27.9.1339

Wu X, Liu Y, Zhang Y, Gu R, 2021. Advances in research on the mechanism of heterosis in plants. Front Plant Sci 12: 745726. https://doi.org/10.3389/fpls.2021.745726

Zhang JL, Cao KF, 2009. Stem hydraulics mediates leaf water status, carbon gain, nutrient use efficiencies and plant growth rates across dipterocarp species. Funct Ecol 23: 658-667. https://doi.org/10.1111/j.1365-2435.2009.01552.x

Published
2024-03-14
How to Cite
Hernández, M. J., Mutke, S., Montes, F., & Pita, P. (2024). Early testing for improving growth under water shortage in Eucalyptus globulus Labill. Forest Systems, 33(1), e01. https://doi.org/10.5424/fs/2024331-20868
Section
Research Articles

Funding data

Ministerio de Ciencia e Innovación
Grant numbers AGL200607886