Foliar water uptake via cork warts in mangroves of the Sonneratia genus.
dehydration
kinetics
pathway
sclereids
seasonality
surface conductance
Journal
Plant, cell & environment
ISSN: 1365-3040
Titre abrégé: Plant Cell Environ
Pays: United States
ID NLM: 9309004
Informations de publication
Date de publication:
09 2021
09 2021
Historique:
revised:
07
06
2021
received:
06
03
2021
accepted:
09
06
2021
pubmed:
13
6
2021
medline:
15
12
2021
entrez:
12
6
2021
Statut:
ppublish
Résumé
Foliar water uptake (FWU) occurs in plants of diverse ecosystems; however, the diversity of pathways and their associated FWU kinetics remain poorly resolved. We characterized a novel FWU pathway in two mangrove species of the Sonneratia genus, S. alba and S. caseolaris. Further, we assessed the influence of leaf wetting duration, wet-dry seasonality and leaf dehydration on leaf conductance to surface water (K
Substances chimiques
Water
059QF0KO0R
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2925-2937Informations de copyright
© 2021 John Wiley & Sons Ltd.
Références
Ball, M. C. (1988). Salinity tolerance in the mangroves Aegiceras corniculatum and Avicennia marina. I. Water use in relation to growth, carbon partitioning, and salt balance. Functional Plant Biology, 15, 447-464.
Ball, M. C., & Pidsley, S. M. (1995). Growth responses to salinity in relation to distribution of two mangrove species, Sonneratia alba and S. lanceolata, in northern Australia. Functional Ecology, 9, 77-85.
Benzing, D. H., & Burt, K. M. (1970). Foliar permeability among twenty species of the Bromeliaceae. Bulletin of the Torrey Botanical Club, 97, 269.
Berry, Z. C., Emery, N. C., Gotsch, S. G., & Goldsmith, G. R. (2019). Foliar water uptake: Processes, pathways, and integration into plant water budgets. Plant, Cell & Environment, 42, 410-423.
Binks, O., Coughlin, I., Mencuccini, M., & Meir, P. (2020). Equivalence of foliar water uptake and stomatal conductance? Plant, Cell & Environment, 43, 524-528.
Binks, O., Meir, P., Rowland, L., Costa, A. C. L., da Vasconcelos, S. S., de Oliveira, A. A. R., … Mencuccini, M. (2016). Plasticity in leaf-level water relations of tropical rainforest trees in response to experimental drought. New Phytologist, 211, 477-488.
Binks, O., Mencuccini, M., Rowland, L., Costa, A. C. L., da Carvalho, C. J. R., de Bittencourt, P., … Meir, P. (2019). Foliar water uptake in Amazonian trees: Evidence and consequences. Global Change Biology, 25, 2678-2690.
Breshears, D. D., McDowell, N. G., Goddard, K. L., Dayem, K. E., Martens, S. N., Meyer, C. W., & Brown, K. M. (2008). Foliar absorption of intercepted rainfall improves woody plant water status most during drought. Ecology, 89, 41-47.
Brodribb, T. J. (2015). Bringing anatomy back into the equation. Plant Physiology, 168, 1461-1461.
Brodribb, T. J., & Holbrook, N. M. (2003). Stomatal closure during leaf dehydration, correlation with other leaf physiological traits. Plant Physiology, 132, 2166-2173.
Brodribb, T. J., & Holbrook, N. M. (2005). Water stress deforms tracheids peripheral to the leaf vein of a tropical conifer. Plant Physiology, 137, 1139-1146.
Bryant, C., Fuenzalida, T. I., Brothers, N., Mencuccini, M., Sack, L., Binks, O., & Ball, M. C. (2021). Shifting access to pools of shoot water sustains gas exchange and increases stem hydraulic safety during seasonal atmospheric drought. Plant, Cell & Environment, 1-14. https://doi.org/10.1111/pce.14080
Buckley, T. N., John, G. P., Scoffoni, C., & Sack, L. (2015). How does leaf anatomy influence water transport outside the xylem? Plant Physiology, 168, 1616-1635.
Burkhardt, J. (2010). Hygroscopic particles on leaves: Nutrients or desiccants? Ecological Monographs, 80, 369-399.
Burkhardt, J., Basi, S., Pariyar, S., & Hunsche, M. (2012). Stomatal penetration by aqueous solutions-An update involving leaf surface particles. New Phytologist, 196, 774-787.
Byrt, C. S., Zhao, M., Kourghi, M., Bose, J., Henderson, S. W., Qiu, J., … Tyerman, S. (2017). Non-selective cation channel activity of aquaporin AtPIP2;1 regulated by Ca2+ and pH. Plant, Cell & Environment, 40, 802-815.
Cavallaro, A., Carbonell, S. L., Pereyra, D. A., Goldstein, G., Scholz, F. G., & Bucci, S. J. (2020). Foliar water uptake in arid ecosystems: seasonal variability and ecophysiological consequences. Oecologia, 193, 337-348.
Chaumont, F., & Tyerman, S. D. (2014). Aquaporins: Highly regulated channels controlling plant water relations. Plant Physiology, 164, 1600-1618.
Chiang, J.-M., Lin, T.-C., Luo, Y.-C., Chang, C.-T., Cheng, J.-Y., & Martin, C. E. (2013). Relationships among rainfall, leaf hydrenchyma, and Crassulacean acid metabolism in Pyrrosia lanceolata (L.) Fraw. (Polypodiaceae) in Central Taiwan. Flora-Morphology, Distribution, Functional Ecology of Plants, 208, 343-350.
Coopman, R. E., Nguyen, H. T., Mencuccini, M., Oliveira, R. S., Sack, L., Lovelock, C. E., & Ball, M. C. (2021). Harvesting water from unsaturated atmospheres: Deliquescence of salt secreted onto leaf surfaces drives reverse sap flow in a dominant arid climate mangrove, Avicennia Marina. New Phytologist. https://doi.org/10.1111/nph.17461
Dawson, T. E., & Goldsmith, G. R. (2018). The value of wet leaves. New Phytologist, 219, 1156-1169.
Duke, N. C. (1992). Chapter 4 - Mangrove floristics and biogeography. In Robertson, A., & Alongi, D. (Eds.), Tropical Mangrove Ecosystems, (pp. 63-100). Washington, DC: the American Geophysical Union.
Duke, N., Ball, M., & Ellison, J. (1998). Factors influencing biodiversity and distributional gradients in mangroves. Global Ecology & Biogeography Letters, 7, 27-47.
Duursma, R. A., Blackman, C. J., Lopéz, R., Martin-StPaul, N. K., Cochard, H., & Medlyn, B. E. (2019). On the minimum leaf conductance: Its role in models of plant water use, and ecological and environmental controls. New Phytologist, 221, 693-705.
Eller, C. B., Lima, A. L., & Oliveira, R. S. (2016). Cloud forest trees with higher foliar water uptake capacity and anisohydric behavior are more vulnerable to drought and climate change. New Phytologist, 211, 489-501.
Evans, L. S., & Bromberg, A. (2010). Characterization of cork warts and aerenchyma in leaves of Rhizophora mangle and Rhizophora racemosa. The Journal of the Torrey Botanical Society, 137, 30-38.
Evans, L. S., Testo, Z. M., & Cerutti, J. A. (2009). Characterization of internal airflow within tissues of mangrove species from Australia: Leaf pressurization processes. The Journal of the Torrey Botanical Society, 136, 70-83.
Evert, R. F. (2006). Esau's plant anatomy: Meristems, cell and tissues of the plant body: Their structure, function, and development (3rd ed.). Hoboken, NJ: John Wiley & Sons.
Ewing, H. A., Weathers, K. C., Templer, P. H., Dawson, T. E., Firestone, M. K., Elliott, A. M., & Boukili, V. K. S. (2009). Fog water and ecosystem function: Heterogeneity in a California redwood Forest. Ecosystems, 12, 417-433.
Farooqui, P. (1982). Cork-warts in Eucalyptus species. Proc. Indian Acad. Sci. (Plant Sci.), 91(4), 289-295.
Fernández, V., Bahamonde, H. A., Javier, P.-P. J., Gil-Pelegrín, E., Sancho-Knapik, D., Gil, L., … Eichert, T. (2017). Physico-chemical properties of plant cuticles and their functional and ecological significance. Journal of Experimental Botany, 68, 5293-5306.
Flowers, T. J., & Colmer, T. D. (2008). Salinity tolerance in halophytes. The New Phytologist, 179, 945-963.
Foster, A. S. (1956). Plant idioplasts: Remarkable examples of cell specialization. Protoplasma, 46, 184-193.
Fuenzalida, T. I., Bryant, C. J., Ovington, L. I., Yoon, H.-J., Oliveira, R. S., Sack, L., & Ball, M. C. (2019). Shoot surface water uptake enables leaf hydraulic recovery in Avicennia marina. New Phytologist, 224, 1504-1511.
Gotsch, S. G., Nadkarni, N., Darby, A., Glunk, A., Dix, M., Davidson, K., & Dawson, T. E. (2015). Life in the treetops: Ecophysiological strategies of canopy epiphytes in a tropical montane cloud forest. Ecological Monographs, 85, 393-412.
Griffith, M. M. (1968). The structure and development of foliar sclereids in Osmanthus fragrans Lour. Phytomorphology, 18, 75-79.
Guzmán-Delgado, P., Earles, J. M., & Zwieniecki, M. A. (2018). Insight into the physiological role of water absorption via the leaf surface from a rehydration kinetics perspective. Plant, Cell & Environment, 41, 1886-1894.
Guzmán-Delgado, P., Laca, E., & Zwieniecki, M. A. (2021). Unravelling foliar water uptake pathways: The contribution of stomata and the cuticle. Plant, Cell & Environment, 44, 1728-1740.
Heide-Jorgensen, H. S. (1990). Xeromorphic leaves of Hakea suaveolens R. Br. IV. Ontogeny, structure and function of the Sclereids. Australian Journal of Botany, 38, 25-43.
Joffily, A., & Cardoso, V. R. (2010). Cork-warts on the leaf epidermis of four genera of Celastroidea-Celastraceae. Flora-Morphology, Distribution, Functional Ecology of Plants, 205, 313-318.
Korn, R. W., & Fredrick, G. W. (1973). Development of D-type stomata in the leaves of Ilex crenata var. convexa. Annals of Botany, 37(3), 647-656.
Kourghi, M., Pei, J. V., Ieso, M. L. D., Nourmohammadi, S., Chow, P. H., & Yool, A. J. (2018). Fundamental structural and functional properties of aquaporin ion channels found across the kingdoms of life. Clinical and Experimental Pharmacology and Physiology, 45, 401-409.
Limm, E. B., Simonin, K. A., Bothman, A. G., & Dawson, T. E. (2009). Foliar water uptake: A common water acquisition strategy for plants of the redwood forest. Oecologia, 161, 449-459.
Losada, J. M., Díaz, M., & Holbrook, N. M. (2020). Idioblasts and peltate hairs as distribution networks for water absorbed by xerophilous leaves. Plant, Cell & Environment, 44(5), 1346-1360.
Malaviya, M. (1976). On the occurence of sclereids in two genera of Myrtaceae. Proceedings of the Indian Academy of Sciences-Section B, 66, 45-52.
Martin, C. E., & von Willert, D. J. (2000). Leaf epidermal hydathodes and the ecophysiological consequences of foliar water uptake in species of Crassula from the Namib desert in southern Africa. Plant Biology, 2, 229-242.
Moon, G. J., Clough, B. F., Peterson, C. A., & Allaway, W. G. (1986). Apoplastic and symplastic pathways in Avicennia marina (Forsk.) Vierh. Roots revealed by fluorescent tracer dyes. Functional Plant Biology, 13, 637-648.
Nguyen, H. T., Meir, P., Wolfe, J., Mencuccini, M., & Ball, M. C. (2017). Plumbing the depths: Extracellular water storage in specialized leaf structures and its functional expression in a three-domain pressure-volume relationship. Plant, Cell & Environment, 40, 1021-1038.
Nguyen, H. T., Stanton, D. E., Schmitz, N., Farquhar, G. D., & Ball, M. C. (2015). Growth responses of the mangrove Avicennia marina to salinity: Development and function of shoot hydraulic systems require saline conditions. Annals of Botany, 115, 397-407.
Nonami, H., & Schulze, E.-D. (1989). Cell water potential, osmotic potential, and turgor in the epidermis and mesophyll of transpiring leaves. Planta, 177, 35-46.
Oliveira, R. S., Eller, C. B., Bittencourt, P. R. L., & Mulligan, M. (2014). The hydroclimatic and ecophysiological basis of cloud forest distributions under current and projected climates. Annals of Botany, 113, 909-920.
Passioura, J. B., Ball, M. C., & Knight, J. H. (1992). Mangroves may salinize the soil and in so doing limit their transpiration rate. Functional Ecology, 6, 476.
R Core Team (2019). R: A language and environment for statistical computing. R Foundation for Statistical Computing. Vienna, Austria. URL http://www.R-project.org/.
Rao, A. N., & Chin, W. Y. (1966). Foliar sclereids in certain members of Annonaceae and Myristicaceae. Flora oder Allgemeine botanische Zeitung. Abt. A, Physiologie Und Biochemie, 156, 220-231.
Rao, A. T., & Mody, K. J. (1961). On terminal sclereids and tracheoid idioblasts. Proceedings of the Indian Academy of Sciences-Section B, 53, 257-262.
Rao, T. A., & Bhupal, O. P. (1973). Typology of sclereids. Proceedings of the Indian Academy of Sciences-Section B, 77, 41-55.
Raux, P. S., Gravelle, S., & Dumais, J. (2020). Design of a unidirectional water valve in Tillandsia. Nature Communications, 11, 396.
Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., … Cardona, A. (2012). Fiji: An open-source platform for biological-image analysis. Nature Methods, 9, 676-682.
Schneider, C. A., Rasband, W. S., & Eliceiri, K. W. (2012). NIH image to ImageJ: 25 years of image analysis. Nature Methods, 9, 671-675.
Schönherr, J., & Bukovac, M. J. (1972). Penetration of stomata by liquids: Dependence on surface tension, wettability, and stomatal morphology. Plant Physiology, 49, 813-819.
Schreel, J. D. M., & Steppe, K. (2020). Foliar water uptake in trees: Negligible or necessary? Trends in Plant Science, 25, 590-603.
Schreel, J. D. M., Van de Wal, B. A. E., Hervé-Fernandez, P., Boeckx, P., & Steppe, K. (2019). Hydraulic redistribution of foliar absorbed water causes turgor-driven growth in mangrove seedlings. Plant, Cell & Environment, 42, 2437-2447.
Schreel, J. D. M., von der Crone, J. S., Kangur, O., & Steppe, K. (2019). Influence of drought on foliar water uptake capacity of temperate tree species. Forests, 10, 562.
Stadelmann, E. J., & Kinzel, H. (1972). Vital staining of plant cells. In D. M. Prescott (Ed.), Methods in cell biology (pp. 325-372). New York: Academic Press.
Steppe, K., Vandegehuchte, M. W., Van de Wal, B. A. E., Hoste, P., Guyot, A., Lovelock, C. E., & Lockington, D. A. (2018). Direct uptake of canopy rainwater causes turgor-driven growth spurts in the mangrove Avicennia marina. Tree Physiology, 38, 979-991.
Tan, W.-K., Lin, Q., Lim, T.-M., Kumar, P., & Loh, C.-S. (2013). Dynamic secretion changes in the salt glands of the mangrove tree species Avicennia officinalis in response to a changing saline environment. Plant, Cell & Environment, 36, 1410-1422.
Tomlinson, P. B. (1959). Structure and distribution of sclereids in the leaves of palms. New Phytologist, 58, 253-266.
Tomlinson, P. B. (1986). The botany of mangroves. Cambridge, UK: Cambridge University Press.
Tyree, M. T., & Tammes, P. M. L. (1975). Translocation of uranin in the symplasm of staminal hairs of Tradescantia. Canadian Journal of Botany, 53, 2038-2046.
Vesala, T., Sevanto, S., Grönholm, T., Salmon, Y., Nikinmaa, E., Hari, P., & Hölttä, T. (2017). Effect of leaf water potential on internal humidity and CO2 dissolution: Reverse transpiration and improved water use efficiency under negative pressure. Frontiers in Plant Science, 8, 54.
Wang, X., Xiao, H., Cheng, Y., & Ren, J. (2016). Leaf epidermal water-absorbing scales and their absorption of unsaturated atmospheric water in Reaumuria soongorica, a desert plant from the northwest arid region of China. Journal of Arid Environments, 128, 17-29.
Yan, X., Zhou, M., Dong, X., Zou, S., Xiao, H., & Ma, X.-F. (2015). Molecular mechanisms of foliar water uptake in a desert tree. AoB PLANTS, 7, plv129.
Yates, D., & Hutley, L. (1995). Foliar uptake of water by wet leaves of Sloanea woollsii, an Australian subtropical rainforest tree. Australian Journal of Botany, 43, 157.