Abstract

Acclimation to fluctuating light environment with short (lasting 20 s, at 650 or 1,250 μmol photons m−2 s−1, every 6 or 12 min) or long (for 40 min at 650 μmol photons m−2 s−1, once a day at midday) sunflecks was studied in Arabidopsis thaliana. The sunfleck treatments were applied in the background daytime light intensity of 50 μmol photons m−2 s−1. In order to distinguish the effects of sunflecks from those of increased daily irradiance, constant light treatments at 85 and 120 μmol photons m−2 s−1, which gave the same photosynthetically active radiation (PAR) per day as the different sunfleck treatments, were also included in the experiments. The increased daily total PAR in the two higher constant light treatments enhanced photosystem II electron transport and starch accumulation in mature leaves and promoted expansion of young leaves in Columbia-0 plants during the 7-day treatments. Compared to the plants remaining under 50 μmol photons m−2 s−1, application of long sunflecks caused upregulation of electron transport without affecting carbon gain in the form of starch accumulation and leaf growth or the capacity of non-photochemical quenching (NPQ). Mature leaves showed marked enhancement of the NPQ capacity under the conditions with short sunflecks, which preceded recovery and upregulation of electron transport, demonstrating the initial priority of photoprotection. The distinct acclimatory responses to constant PAR, long sunflecks, and different combinations of short sunflecks are consistent with acclimatory adjustment of the processes in photoprotection and carbon gain, depending on the duration, frequency, and intensity of light fluctuations. While the responses of leaf expansion to short sunflecks differed among the seven Arabidopsis accessions examined, all plants showed NPQ upregulation, suggesting limited ability of this species to utilize short sunflecks. The increase in the NPQ capacity was accompanied by reduced chlorophyll contents, higher levels of the xanthophyll-cycle pigments, faster light-induced de-epoxidation of violaxanthin to zeaxanthin and antheraxanthin, increased amounts of PsbS protein, as well as enhanced activity of superoxide dismutase. These acclimatory mechanisms, involving reorganization of pigment–protein complexes and upregulation of other photoprotective reactions, are probably essential for Arabidopsis plants to cope with photo-oxidative stress induced by short sunflecks without suffering from severe photoinhibition and lipid peroxidation.

Highlights

  • Light in natural environments is highly variable in both intensity and spectral composition

  • The results show distinct effects of constant photosynthetically active radiation (PAR), LSF, and SSF on acclimation of Col-0 plants and highlight strong photoprotective responses to SSF that are conserved in different Arabidopsis accessions

  • Changes in photosystem II (PSII) activity during acclimation to different sunfleck conditions Acclimation of PSII activity to sunfleck conditions was studied in mature leaves of Col-0 plants by measuring Chl a fluorescence

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Summary

Introduction

Light in natural environments is highly variable in both intensity and spectral composition. Pronounced temporal fluctuations and spatial heterogeneity characterize the dynamic nature of light environment. Irregular changes in light environment occur in various ways, but the most common causes include variation in weather and cloud movement, development and destruction of leaves, branches, or canopy, and fluttering of leaves by wind. Shortterm fluctuation of light occurs in forest understorey or inside dense crop canopies. In both cases, rays of sunlight penetrate the canopy in the form of ‘‘sunflecks’’ to expose shade-grown leaves and plants to bursts of high light (HL). Sunflecks account for 20*80 % of photosynthetically active radiation (PAR) available for understorey plants growing in different types of forests, or 40*90 % within soybean canopies (Pearcy 1990 and references therein). Sunfleck utilization efficiency, e.g., due to photosynthetic induction and induction loss (Chazdon and Pearcy 1986a; Pons et al 1992), has been of ecological and agricultural interest

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