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AOBPreview originally published online on May 30, 2006
Annals of Botany 2006 98(1):267-275; doi:10.1093/aob/mcl100
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© The Author 2006. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Physiological Effects of Kaolin Applications in Well-irrigated and Water-stressed Walnut and Almond Trees

A. ROSATI1,*, S. G. METCALF2, R. P. BUCHNER3, A. E. FULTON3 and B. D. LAMPINEN2

1 Istituto Sperimentale per l'Olivicoltura, Via Nursina 2, 06049 Spoleto, (PG) Italy, 2 Department of Plant Sciences, University of California, Mail stop #2, One Shields Avenue, Davis, CA 95616, USA and 3 University of California Cooperative Extension, Tehama County, 1754 Walnut Street, Red Bluff, CA 96080, USA

* For correspondence. E-mail adolfo.rosati{at}entecra.it

Received: 30 January 2006    Returned for revision: 22 February 2006    Accepted: 17 March 2006    Published electronically: 30 May 2006

Background and Aims Kaolin applications have been used to mitigate the negative effects of water and heat stress on plant physiology and productivity with variable results, ranging from increased to decreased yields and photosynthetic rates. The mechanisms of action of kaolin applications are not clear: although the increased albedo reduces leaf temperature and the consequent heat stress, it also reduces the light available for photosynthesis, possibly offsetting benefits of lower temperature. The objective of this study was to investigate which of these effects are prevalent and under which conditions.

Methods A 6 % kaolin suspension was applied on well-irrigated and water-stressed walnut (Juglans regia) and almond (Prunus dulcis) trees. Water status (i.e. stem water potential, {Psi}s), gas exchange (i.e. light-saturated CO2 assimilation rate, Amax; stomatal conductance, gs), leaf temperature (Tl) and physiological relationships in treated and control trees were then measured and compared.

Key Results In both species, kaolin did not affect the daily course of {Psi}s whereas it reduced Amax by 1–4 µmol CO2 m–2 s–1 throughout the day in all combinations of species and irrigation treatments. Kaolin did not reduce gs in any situation. Consequently, intercellular CO2 concentration (Ci) was always greater in treated trees than in controls, suggesting that the reduction of Amax with kaolin was not due to stomatal limitations. Kaolin reduced leaf temperature (Tl) by about 1–3 °C and leaf-to-air vapour pressure difference (VPDl) by about 0·1–0·7 kPa. Amax was lower at all values of gs, Tl and VPDl in kaolin-treated trees. Kaolin affected the photosynthetic response to the photosynthetically active radiation (PAR) in almond leaves: kaolin-coated leaves had similar dark respiration rates and light-saturated photosynthesis, but a higher light compensation point and lower apparent quantum yield, while the photosynthetic light-response curve saturated at higher PAR. When these parameters were used to model the photosynthetic response curve to PAR, it was estimated that the kaolin film allowed 63 % of the incident PAR to reach the leaf.

Conclusions The main effect of kaolin application was the reduction, albeit minor, of photosynthesis, which appeared to be related to the shading of the leaves. The reduction in Tl and VPDl with kaolin did not suffice to mitigate the adverse effects of heat and water stress on Amax.

Key words: Juglans regia, kaolin particle film, photosynthesis, Prunus dulcis, stomatal conductance, water potential, stress


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