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Understanding the response of leaf hydraulic conductance (Kleaf) to light is a challenge in elucidating plant–water relationships. Recent data have shown that the effect of light on Kleaf is not systematically related to aquaporin regulation, leading to conflicting conclusions. Here we investigated the relationship between light, Kleaf, and aquaporin transcript levels in five tree species (Juglans regia L., Fagus sylvatica L., Quercus robur L., Salix alba L. and Populus tremula L.) grown in the same environmental conditions, but differing in their Kleaf responses to light. Moreover, the Kleaf was measured by two independent methods (high-pressure flow metre (HPFM) and evaporative flux method (EFM)) in the most (J. regia) and least (S. alba) responsive species and the transcript levels of aquaporins were analyzed in perfused and unperfused leaves. Here, we found that the light-induced Kleaf value was closely related to stronger expression of both the PIP1 and PIP2 aquaporin genes in walnut (J. regia), but to stimulation of PIP1 aquaporins alone in F. sylvatica and Q. robur. In walnut, all newly identified aquaporins were found to be upregulated in the light and downregulated in the dark, further supporting the relationship between the light-mediated induction of Kleaf and aquaporin expression in walnut. We also demonstrated that the Kleaf response to light was quality-dependent, Kleaf being 60% lower in the absence of blue light. This decrease in Kleaf was correlated with strong downregulation of three PIP2 aquaporins and of all the PIP1 aquaporins tested. These data support a relationship between light-mediated Kleaf regulation and the abundance of aquaporin transcripts in the walnut tree. [ABSTRACT FROM PUBLISHER]

Abstract: Heavy metals (HMs) are known to have negative effects on plant water status; however, the mechanisms by which plants rearrange their water relations to adapt to such conditions are poorly understood. Using the model plant Mesembryanthemum crystallinum, we studied disturbances in water status and rapid plant defence responses induced by excess copper or zinc. After a day of HM stress, reductions in root sap exudation and water deficits in leaf tissues became evident. We also observed several primary adaptive events, including a rapid decrease in the transpiration rate and progressive declines in the leaf-cell sap osmotic potential. Longer HM treatments resulted in reductions of total and relative water contents as well as proline accumulation, an increase in water retention capacity and changes in aquaporin gene expression. After 3h of HM exposure, leaf expression of the McTIP2;2 gene, which encodes tonoplast aquaporin, was suppressed more than two-fold, thus representing one of the earliest responses to HM treatment. The expression of three additional aquaporin genes was also reduced starting at 9h; this effect became more prominent upon longer HM exposure. These results indicate that HMs induce critical rearrangements in the water relations of M. crystallinum plants, based on the rapid suppression of transpiration flow and strong inhibition of root sap exudation. These effects then triggered an adaptive water-conserving strategy involving differential regulation of aquaporin gene expression in leaves and roots, further reductions in transpiration, and an accelerated switch to CAM photosynthesis. [Copyright &y& Elsevier]