Planta

, Volume 246, Issue 6, pp 1069–1082 | Cite as

Quantification of light screening by anthocyanins in leaves of Berberis thunbergii

Original Article
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Abstract

Main conclusion

Up to 40% of incident light was screened in red Berberis leaves in vivo by anthocyanins, resulting also in up to 40% reduction of light-limited photosynthesis.

The biological function of anthocyanins in leaves has been strongly discussed, but the hypothesis of a screening function is favored by most authors. For an evaluation of the function as photoprotective pigments, a quantification of their screening of the mesophyll is important. Here, chlorophyll fluorescence excitation of leaves of a red and a green variety of Berberis thunbergii was used to estimate the extent of screening by anthocyanins at 545 nm and over the whole photosynthetically active wavelength range. Growth at high light (430 µmol m−2 s−1) resulted in 90% screening at 545 nm corresponding to 40–50% screening over the whole wavelength range, depending on the light source. The concomitant reduction of photosynthetic quantum yield was of the same size as the calculated reduction of light reaching the chloroplasts. The induction of anthocyanins in the red variety also enhanced the epoxidation state of the violaxanthin cycle under growth conditions, indicating that red leaves were suffering less from excessive irradiance. Pool sizes of violaxanthin cycle carotenoids indicated a shade acclimation of the light harvesting complexes in red leaves. The observed reduction of internal light in anthocyanic leaves has by necessity a photoprotective effect.

Keywords

Anthocyanins Chlorophyll fluorescence excitation Light screening Photoprotection Photosynthetic quantum yield Violaxanthin cycle 

Abbreviations

EPS

Epoxidation state of the violaxanthin cycle

F545 (F650)

Chlorophyll fluorescence excited by 545 nm (650 nm)

PAR

Photosynthetically active radiation

PPFD

Photosynthetic photon flux density

Notes

Acknowledgements

Anneke Kramm and Jens Hermann are thanked for help with pigment determination.

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Copyright information

© Springer-Verlag GmbH Germany 2017

Authors and Affiliations

  1. 1.Botanical InstituteChristian-Albrechts University KielKielGermany

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