Skip to main content
Log in

Seasonal changes in photoprotective mechanisms of leaves from shaded and unshaded field-grown coffee (Coffea arabica L.) trees

  • Original Paper
  • Published:
Trees Aims and scope Submit manuscript

Abstract

Coffee is native to shady environments, but often grows and yields better without shade. Thus, it may be reasoned that coffee leaves should display enough plasticity to acclimate themselves to contrasting light environments. However, little is known about mechanisms associated with such plasticity in coffee. This work aimed, therefore, to explore differences in leaf photoprotective mechanisms. Plants were grown in the field and received either 48 or 100% natural light. Evaluations were made using outer leaves from the sun-facing sides of the coffee hedgerow in Viçosa (Brazil) in August and October, when growth and photosynthetic rates are expected to be minimal and maximal, respectively, and in December, when temporary depressions in those variables are common. Regardless of light treatments, coffee leaves showed: (1) very low photosynthetic rates (generally below 2.5 μmol m−2 s−1), (2) chronic photoinhibition in August (dry, cool season) that was accompanied by strong loss of pigment concentration, and (3) discrete, dynamic photoinhibition in October and December (rainy, warm season). Compared with shaded leaves, sunlit leaves generally exhibited lower pigment concentration, lower quantum yield of electron transport, steeper inclinations and similar electron transport rate. Total ascorbate pool tended to be larger in sunlit than in shaded leaves (but with similar redox state), whereas activities of key antioxidant enzymes, as well as malondialdehyde accumulation and electrolyte leakage, were similar between those leaf types. As a whole, the photosynthetic apparatus of the coffee tree showed a low phenotypic plasticity to varying irradiance.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Adams WW III, Baker DH (1998) Seasonal changes in xanthophyll cycle-dependent energy dissipation in Yucca glauca Nuttall. Plant Cell Environ 21:501–511

    Article  CAS  Google Scholar 

  • Adams WW, Zarter CR, Ebbert V, Demmig-Adams B (2004) Photoprotective strategies of owerwintering evergreens. BioScience 54:41–49

    Article  Google Scholar 

  • Allen DJ, Ort DR (2001) Impacts of chilling temperatures on photosynthesis in warm-climate plants. Trends Plant Sci 6:36–42

    Article  PubMed  CAS  Google Scholar 

  • Asada K (1999) The water–water cycle in chloroplasts: scavenging of active oxygens and dissipation of excess photons. Annu Rev Plant Physiol Plant Mol Biol 50:601–639

    Article  PubMed  CAS  Google Scholar 

  • Beer J, Muschler R, Kass D, Somarriba E (1998) Shade management in coffee and cacao plantations. Agrofor Syst 38:139–164

    Article  Google Scholar 

  • Björkman O, Demmig B (1987) Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins. Planta 170:489–504

    Article  Google Scholar 

  • DaMatta FM, Maestri M, Mosquim PR, Barros RS (1997) Photosynthesis in coffee (Coffea arabica and C. canephora) as affected by winter and summer conditions. Plant Sci 128:43–50

    Article  CAS  Google Scholar 

  • DaMatta FM, Amaral JAT, Rena AB (1999) Growth periodicity in trees of Coffea arabica L. in relation to nitrogen supply and nitrate reductase activity. Field Crops Res 60:223–229

    Article  Google Scholar 

  • DaMatta FM, Loos RA, Rodrigues R, Barros RS (2001) Actual and photosynthetic rates of tropical crop species. Braz J Plant Physiol 13:24–32

    Google Scholar 

  • DaMatta FM (2004) Ecophysiological constraints on the production of shaded and unshaded coffee: a review. Field Crops Res 86:99–114

    Article  Google Scholar 

  • Demmig-Adams B, Adams WW III (1992) Photoprotection and other responses of plants to high light stress. Annu Rev Plant Physiol Plant Mol Biol 43:599–626

    Article  CAS  Google Scholar 

  • Demmig-Adams B, Adams WW III, Baker DH, Logan BA, Bowling DR, Verhoeven AS (1996) Using chlorophyll fluorescence to assess the fraction of absorbed light allocated to thermal dissipation of excess excitation. Physiol Plant 98:253–264

    Article  CAS  Google Scholar 

  • Dias PC (2006) Variação espacial da fotossíntese e de mecanismos de fotoproteção no cafeeiro (Coffea arabica L.). M.Sc. Thesis, Universidade Federal de Viçosa, Brazil, p 49

  • Evans J (1993) Photosynthetic acclimation and nitrogen partitioning within a Lucerne canopy. II. Stability through time and comparison with a theoretical optimum. Aust J Plant Physiol 20:69–82

    Article  CAS  Google Scholar 

  • Falster DS, Westoby M (2003) Leaf size and angle vary widely across species: what consequences for light interception? New Phytol 158:509–525

    Article  Google Scholar 

  • Franck N, Vaast P, Génard M, Dauzat J (2006) Soluble sugars mediate sink feedback down-regulation of leaf photosynthesis in field-grown Coffea arabica. Tree Physiol 26:517–525

    PubMed  CAS  Google Scholar 

  • Genty B, Briantais JM, Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990:87–92

    CAS  Google Scholar 

  • Gilmore AM (1997) Mechanistic aspects of xanthophyll cycle-dependent photoprotection in higher plant chloroplasts and leaves. Physiol Plant 99:197–209

    Article  CAS  Google Scholar 

  • Huner NPA, Öquist G, Sarhan F (1998) Energy balance and acclimation to light and cold. Trends Plant Sci 3:224–230

    Article  Google Scholar 

  • James SA, Bell DT (2000) Leaf orientation, light interception and stomatal conductance of Eucalyptus globulus ssp. globulus leaves. Tree Physiol 20:815–823

    PubMed  Google Scholar 

  • Kitao M, Utsugi H, Kuramoto S, Tabuchi R, Fujimoto K, Lihpai S (2003) Light-dependent photosynthetic characteristics indicated by chlorophyll fluorescence in five mangrove species native to Pohnpei Island, Micronesia. Physiol Plant 117:376–382

    Article  PubMed  CAS  Google Scholar 

  • Landsberg JJ (1986) Physiological ecology of forest production. Academic Press, San Diego

    Google Scholar 

  • Lichtenthaler HK (1987) Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. Meth Enzimol 148:350–382

    Article  CAS  Google Scholar 

  • Lima ALS, DaMatta FM, Pinheiro HA, Tótola MR, Loureiro ME (2002) Photochemical responses and oxidative stress in two clones of Coffea canephora under water-deficit conditions. Environ Exp Bot 47:239–247

    Article  CAS  Google Scholar 

  • Logan BA, Kornyeyev D, Hardison J, Holaday AS (2006) The role of antioxidant enzymes in photoprotection. Photosynth Res 88:119–132

    Article  PubMed  CAS  Google Scholar 

  • Niyogi KK (1999) Photoprotection revisited: genetic and molecular approaches. Annu Rev Plant Physiol Plant Mol Biol 50:333–359

    Article  PubMed  CAS  Google Scholar 

  • Norman JW, Campbell GS (1989) Canopy structure. In: Pearcy RW, Ehleringer JR, Mooney HA, Rundel PW (eds) Plant physiological ecology: field methods and instrumentation. British Library, London, pp 301–323

    Google Scholar 

  • Öquist G, Huner NPA (2003) Photosynthesis of owerwintering evergreen plants. Annu Rev Plant Biol 54:329–355

    Article  PubMed  CAS  Google Scholar 

  • Ort DR, Baker NR (2002) A photoprotective role for O2 as an alternative electron sink in photosynthesis? Curr Opin Plant Biol 5:193–198

    Article  PubMed  CAS  Google Scholar 

  • Ottander C, Campbell D, Öquist G (1995) Seasonal changes in photosystem II organization and pigment composition in Pinus sylvestris. Planta 197:176–183

    Article  CAS  Google Scholar 

  • Pearcy RW (1989) Radiation and light measurements. In: Pearcy RW, Ehleringer JR, Mooney HA, Rundel PW (eds) Plant physiological ecology: field methods and instrumentation. British Library, London, pp 97–113

    Google Scholar 

  • Pinheiro HA, DaMatta FM, Chaves ARM, Fontes EPB, Loureiro ME (2004) Drought tolerance in relation to protection against oxidative stress in clones of Coffea canephora subjected to long-term drought. Plant Sci 167:1307–1314

    Article  CAS  Google Scholar 

  • Ramalho JC, Quartin VL, Leitão E, Campos PS, Carelli MLC, Fahl JI, Nunes MA (2003) Cold acclimation ability and photosynthesis among species of the tropical Coffea genus. Plant Biol 5:631–641

    Article  CAS  Google Scholar 

  • Ronquin JC, Prado CHBA, Novaes P, Fahl JI, Ronquin CC (2006) Carbon gain in Coffea arabica during clear and cloudy days in the wet season. Exp Agric 42:147–164

    Article  CAS  Google Scholar 

  • Silva EA, DaMatta FM, Ducatti C, Regazzi AJ, Barros RS (2004) Seasonal changes in vegetative growth and photosynthesis in Arabica coffee trees. Field Crops Res 89:349–357

    Article  Google Scholar 

  • Streb P, Feierabend J (1999) Significance of antioxidants and electron sinks for the cold-hardening-induced resistance of winter rye leaves to photo-oxidative stress. Plant Cell Environ 22:1225–1237

    Article  CAS  Google Scholar 

  • Vaast P, Angrand J, Franck N, Dauzat J, Génard M (2005) Fruit load and ring-barking affect carbon allocation and photosynthesis of leaf and fruit of Coffea arabica in the field. Tree Physiol 25:753–760

    PubMed  CAS  Google Scholar 

  • Valladares F, Martinez-Ferri E, Balaguer L, Perez-Carona E, Manrique E (2000) Low leaf-level response to light and nutrients in Mediterranean evergreen oaks: a conservative resource-use strategy? New Phytol 148:79–91

    Article  CAS  Google Scholar 

  • Verhoeven AS, Swanberg A, Thao M, Whiteman J (2005) Seasonal changes in leaf antioxidant systems and xanthophyll cycle characteristics in Taxus x media growing in sun and shade environments. Physiol Plant 123:428–434

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This research was supported by the Foundation for Research Assistance of the Minas Gerais State, Brazil (Grant CAG 892/04) and by the National Council for Scientific and Technological Development (Grant 303351/2004-7) to F.M. DaMatta. A.R.M. Chaves was supported by a CAPES graduate scholarship from the Brazilian government. H.A. Pinheiro was supported by a post-doctorate fellowship from the Brazilian Consortium for Coffee Research and Development.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Fábio M. DaMatta.

Additional information

Communicated by M. Buckeridge.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Chaves, A.R.M., Ten-Caten, A., Pinheiro, H.A. et al. Seasonal changes in photoprotective mechanisms of leaves from shaded and unshaded field-grown coffee (Coffea arabica L.) trees. Trees 22, 351–361 (2008). https://doi.org/10.1007/s00468-007-0190-7

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00468-007-0190-7

Keywords

Navigation