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Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Anthocyanin influence on light absorption within juvenile and senescing sugar maple leaves – do anthocyanins function as photoprotective visible light screens?

Abby K. van den Berg A C , Thomas C. Vogelmann B and Timothy D. Perkins A
+ Author Affiliations
- Author Affiliations

A Proctor Maple Research Center, The University of Vermont, PO Box 233, Underhill Center, VT 05490, USA.

B Department of Plant Biology, The University of Vermont, Marsh Life Science Building, Burlington, VT 05405, USA.

C Corresponding author. Email: abby.vandenberg@uvm.edu

Functional Plant Biology 36(9) 793-800 https://doi.org/10.1071/FP09030
Submitted: 4 February 2009  Accepted: 15 July 2009   Published: 3 September 2009

Abstract

Foliar anthocyanins are hypothesised to function as photoprotective visible light screens, preventing over-excitation of the photosynthetic system, and decreasing the likelihood of photo-oxidative stress by absorbing green light and reducing the amount of light available to be absorbed by chloroplasts in deeper tissue layers. Chlorophyll fluorescence imaging was used to test the hypothesis that anthocyanins in the palisade mesophyll of juvenile and senescing sugar maple (Acer saccharum Marsh.) leaves function as visible light screens by assessing their influence on light absorption profiles within leaves. We hypothesised that an effective anthocyanic light screen should reduce light absorption, particularly of green wavelengths, by chloroplasts in the spongy mesophyll. Both anthocyanic juvenile and senescing leaves absorbed greater amounts of green light than corresponding nonanthocyanic leaves. However, profiles of green light absorption by chlorophyll within anthocyanic leaves were not shifted to reflect reduced absorption of green light by spongy mesophyll chloroplasts. Further, the spongy mesophyll of both anthocyanic juvenile and senescing leaves absorbed proportions of green light equal to or greater than the spongy mesophyll of corresponding nonanthocyanic leaves. These results indicate that though they may provide a general source of photoprotection by reducing the total quantity of light available to be absorbed by chlorophyll, the anthocyanins in juvenile and senescing sugar maple leaves do not attenuate light in a manner consistent with that expected for an anthocyanic screen in the palisade mesophyll.

Additional keywords: chlorophyll fluorescence, leaf expansion, leaf senescence, photoinhibition, photo-oxidative stress, photoprotection.


Acknowledgements

We thank Nathan Poirier for technical assistance and Drs Paul Schaberg and William Currier for their helpful comments on this research.


References


Archetti M, Döring TF, Hagen SB, Hughes NM, Leather SR , et al . (2009) Unravelling the evolution of autumn colours: an interdisciplinary approach. Trends in Ecology & Evolution 24, 166–173.
Crossref | GoogleScholarGoogle Scholar | open url image1

Baker NR (1985) Energy transduction during leaf growth. In ‘Control of leaf growth’. (Eds NR Baker, WJ Davies, CK Ong) pp. 113–133. (Cambridge University Press: New York)

Burger J, Edwards GE (1996) Photosynthetic efficiency and photodamage by UV and visible radiation, in red versus green leaf Coleus varieties. Plant & Cell Physiology 37, 395–399. open url image1

Chalker-Scott L (1999) Environmental significance of anthocyanins in plant stress responses. Photochemistry and Photobiology 70, 1–9.
Crossref | GoogleScholarGoogle Scholar | open url image1

Esteban R, Fernández-Marin B, Becerril JM, García-Plazaola JI (2008) Photoprotective implications of leaf variegation in E. dens-canis L. and P. officinalis L. Journal of Plant Physiology 165, 1255–1263.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Feild TS, Lee DW, Holbrook NM (2001) Why leaves turn red in autumn. The role of anthocyanins in senescing leaves of red-osier dogwood. Plant Physiology 127, 566–574.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Gould KS, Markham KR, Smith RH, Goris JJ (2000) Functional role of anthocyanins in the leaves of Quintinia serrata A.Cunn. Journal of Experimental Botany 51, 1107–1115.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Gould KS, Neill SO, Vogelmann TC (2002a) A unified explanation for anthocyanins in leaves? Advances in Botanical Research 37, 167–192.
Crossref | GoogleScholarGoogle Scholar | open url image1

Gould KS, Vogelmann TC, Han T, Clearwater MJ (2002b) Profiles of photosynthesis within red and green leaves of Quintinia serrata A.Cunn. Physiologia Plantarum 116, 127–133.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Hoch WA, Singsaas EL, McCown BH (2003) Resorption protection. Anthocyanins facilitate nutrient recovery in autumn by shielding leaves from potentially damaging light levels. Plant Physiology 133, 1296–1305.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Hormaetxe K, Becerril JM, Fleck I, Pintó M, García-Plazaola JI (2005) Functional role of red (retro)-carotenoids as passive light filters in the leaves of Buxus sempervirens L.: increased protection of photosynthetic tissues? Journal of Experimental Botany 56, 2629–2636.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Hughes NM, Neufeld HS, Burkey KO (2005) Functional role of anthocyanins in high-light winter leaves of the evergreen herb Galax urceolata. New Phytologist 168, 575–587.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Ishikura N (1973) The changes in anthocyanin and chlorophyll content during the autumnal reddening of leaves. Kumamoto Journal of Science. Biology 11, 43–50. open url image1

Karageorgou P, Manetas Y (2006) The importance of being red when young: anthocyanins and the protection of young leaves of Quercus coccifera from insect herbivory and excess light. Tree Physiology 26, 613–621.
PubMed |
open url image1

Krupinska K , Humbeck K (2004) Photosynthesis and chloroplast breakdown. In ‘Plant cell death processes’. (Ed. LM Nooden) pp. 169–183. (Academic Press: London)

Kyparissis A, Grammatikopoulos G, Manetas Y (2007) Leaf morphological and physiological adjustments to the spectrally selective shade imposed by anthocyanins in Prunus cerasifera. Tree Physiology 27, 849–857.
PubMed |
open url image1

Kytridis V, Karageorgou P, Levizou E, Manetas Y (2008) Intra-species variation in transient accumulation of leaf anthocyanins in Cistus creticus during winter: evidence that anthocyanins may compensate for an inherent photosynthetic and photoprotective inferiority of the red-leaf phenotype. Journal of Plant Physiology 165, 952–959.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Lee DW (2002) Anthocyanins in leaves: distribution, phylogeny and development. Advances in Botanical Research 37, 38–51. open url image1

Lee DW, O’Keefe J, Holbrook NM, Field TS (2003) Pigment dynamics and autumn leaf senescence in a New England deciduous forest, eastern USA. Ecological Research 18, 677–694.
Crossref | GoogleScholarGoogle Scholar | open url image1

Lev-Yadun S, Gould KS (2007) What do red and yellow autumn leaves signal? Botanical Review 73, 279–289.
Crossref | GoogleScholarGoogle Scholar | open url image1

Lichtenthaler HK, Wellburn AR (1983) Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochemical Society Transactions 603, 591–592. open url image1

Manetas Y (2006) Why some leaves are anthocyanic and why most anthocyanic leaves are red? Flora 201, 163–177. open url image1

Manetas Y, Drinia A, Petropoulou Y (2002) High contents of anthocyanins in young red leaves are correlated with low pools of xanthophyll cycle components and low risk of photoinhibition. Photosynthetica 40, 349–354.
Crossref | GoogleScholarGoogle Scholar | open url image1

Manetas Y, Petropoulou Y, Psaras GK, Drinia A (2003) Exposed red (anthocyanic) leaves of Quercus coccifera display shade characteristics. Functional Plant Biology 30, 265–270.
Crossref | GoogleScholarGoogle Scholar | open url image1

Mendez M, Gwynn-Jones D, Manetas Y (1999) Enhanced UV-B radiation under field conditions increases anthocyanin and reduces the risk of photoinhibition but does not affect growth in the carnivorous plant Pinguicula vulgaris. New Phytologist 144, 275–282.
Crossref | GoogleScholarGoogle Scholar | open url image1

Murray JR, Hackett WP (1991) Dihydroflavonol reductase activity in relation to differential anthocyanin accumulation in juvenile and mature phase Hedera helix L. Plant Physiology 97, 343–351.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Pietrini F, Iannelli MA, Massacci A (2002) Anthocyanin accumulation in the illuminated surface of maize leaves enhances protection from photo-inhibitory risks at low temperature, without further limitation to photosynthesis. Plant, Cell & Environment 25, 1251–1259.
Crossref | GoogleScholarGoogle Scholar | open url image1

Steyn WJ, Wand SJE, Holcroft DM, Jacobs G (2002) Anthocyanins in vegetative tissues: a proposed unified function in photoprotection. New Phytologist 155, 349–361.
Crossref | GoogleScholarGoogle Scholar | open url image1

Vogelmann TC, Evans JR (2002) Profiles of light absorption and chlorophyll within spinach leaves from chlorophyll fluorescence. Plant, Cell & Environment 25, 1313–1323.
Crossref | GoogleScholarGoogle Scholar | open url image1

Vogelmann TC, Han T (2000) Measurement of profiles of absorbed light within spinach leaves. Plant, Cell & Environment 23, 1303–1311.
Crossref | GoogleScholarGoogle Scholar | open url image1