Skip to main content
Log in

Acclimations to light quality on plant and leaf level affect the vulnerability of pepper (Capsicum annuum L.) to water deficit

  • Regular Paper
  • Published:
Journal of Plant Research Aims and scope Submit manuscript

Abstract

We investigated the influence of light quality on the vulnerability of pepper plants to water deficit. For this purpose plants were cultivated either under compact fluorescence lamps (CFL) or light-emitting diodes (LED) providing similar photon fluence rates (95 µmol m−2 s−1) but distinct light quality. CFL emit a wide-band spectrum with dominant peaks in the green and red spectral region, whereas LEDs offer narrow band spectra with dominant peaks at blue (445 nm) and red (665 nm) regions. After one-week acclimation to light conditions plants were exposed to water deficit by withholding irrigation; this period was followed by a one-week regeneration period and a second water deficit cycle. In general, plants grown under CFL suffered more from water deficit than plants grown under LED modules, as indicated by the impairment of the photosynthetic efficiency of PSII, resulting in less biomass accumulation compared to respective control plants. As affected by water shortage, plants grown under CFL had a stronger decrease in the electron transport rate (ETR) and more pronounced increase in heat dissipation (NPQ). The higher amount of blue light suppressed plant growth and biomass formation, and consequently reduced the water demand of plants grown under LEDs. Moreover, pepper plants exposed to high blue light underwent adjustments at chloroplast level (e.g., higher Chl a/Chl b ratio), increasing the photosynthetic performance under the LED spectrum. Differently than expected, stomatal conductance was comparable for water-deficit and control plants in both light conditions during the stress and recovery phases, indicating only minor adjustments at the stomatal level. Our results highlight the potential of the target-use of light quality to induce structural and functional acclimations improving plant performance under stress situations.

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
Fig. 6

Similar content being viewed by others

Abbreviations

A:

Absorbance

c:

Control

das:

Days after sowing

D:

Diameter

CFL:

Compact fluorescence lamps

Chl:

Chlorophyll

DM:

Dry mass

ETR:

Electron transport rate

F:

Fluorescence yield

Fm :

Maximum chlorophyll fluorescence of a dark adapted leaf

Fm´:

Maximum chlorophyll fluorescence in the light adapted state

F0 :

Ground fluorescence of a dark adapted leaf

Fv :

Variable chlorophyll a fluorescence level from a dark adapted leaf (Fv = Fm − F0)

FM:

Fresh mass

Gs:

Stomatal conductance

LED:

Light-emitting diode

NPQ:

Non-photochemical quenching

PAR:

Photosynthetic active radiation

PSI:

Photosystem I

PSII:

Photosystem II

ROS:

Reactive oxygen species

wd:

Water deficit

Vol:

Volume

References

  • Abidi F, Girault T, Douillet O, Guillemain G, Sintes G, Laffaire M, Ben Ahmed H, Smiti S, Huché-Thélier L, Leduc N (2012) Blue light effects on rose photosynthesis and photomorphogenesis. Plant Biol 15:67–74

    Article  PubMed  Google Scholar 

  • Alvino A, Centritto M, De Lorenzi F (1994) Photosynthesis response of sunlit and shade pepper (Capsicum annuum) leaves at different positions in the canopy under two water regimes. Aust J Plant Physiol 21:377–391

    Article  Google Scholar 

  • Anderson JM, Chow WS, Park YI (1995) The grand design of photosynthesis: acclimation of the photosynthetic apparatus to environmental cues. Photosynth Res 46:129–139

    Article  CAS  PubMed  Google Scholar 

  • Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water stress studies. Plant Soil 39:205–207

    Article  CAS  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  PubMed  Google Scholar 

  • Björkman O, Powles SB (1984) Inhibition of photosynthetic reactions under water stress: interaction with light level. Planta 161:490–504

    Article  PubMed  Google Scholar 

  • Brown CS, Schuerger AC, Sager JC (1995) Growth and photomorphogenesis of pepper plants under red light-emitting diodes with supplemental blue or far-red lighting. J Am Soc Hortic Sci 120:808–813

    CAS  PubMed  Google Scholar 

  • Bürling K, Ducruet J-M, Cornic G, Hunsche M, Cerovic ZG (2014) Assessment of photosystem II thermoluminescence as a tool to investigate the effects of dehydration and rehydration on the cyclic/chlororespiratory electron pathways in wheat and barley leaves. Plant Sci 223:116–123

    Article  PubMed  Google Scholar 

  • Buschmann C, Meier D, Kleudgen HK, Lichtenthaler HK (1978) Regulation of chloroplast development by red and blue light. Photochem Photobiol 27:195–198

    Article  CAS  Google Scholar 

  • Chaerle L, Van Der Straeten D (2000) Imaging techniques and the early detection of plant stress. Trends Plant Sci 5(11):495–501

    Article  CAS  PubMed  Google Scholar 

  • Chaerle L, Van Der Straeten D (2001) Seeing is believing: imaging techniques to monitor plant health. Biochem Biophys Acta 1519:153–166

    CAS  PubMed  Google Scholar 

  • Chaves MM (1991) Effects of water deficits on carbon assimilation. J Exp Bot 42:1–16

    Article  CAS  Google Scholar 

  • Chen C, Xiao Y-G, Li X, Ni M (2012) Light-regulated stomatal aperture in Arabidopsis. Mol Plant 5:566–572

    Article  PubMed  Google Scholar 

  • Chow WS, Melis A, Anderson JM (1990) Adjustments of photosystem stoichiometry in chloroplast improve the quantum efficiency of photosynthesis. Proc Natl Acad Sci USA 87:7502–7506

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • De Pascale S, Ruggiero C, Barbieri G (2003) Physiological responses of pepper to salinity and drought. J Am Soc Hortic Sci 128:48–54

    Google Scholar 

  • Delfine S, Loreto F, Alvino A (2001) Drought-stress effects on physiology, growth and biomass production of rainfed and irrigated bell pepper plants in the mediterranean region. J Am Soc Hortic Sci 126:297–304

    CAS  Google Scholar 

  • Demmig-Adams B, Adams WW III (2003) Photoprotection against excess light via zeaxanthin-dependent energy dissipation. In: Larcher W (ed) Physiological plant ecology. Springer, Heidelberg, pp 359–360

    Google Scholar 

  • Dietzel L, Bräutigam K, Pfannschmidt T (2008) Photosynthetic acclimation: state transitions and adjustment of photosystem stoichiometry—functional relationships between short-term and long-term light quality acclimation in plants. FEBS J 275:1080–1088

    Article  CAS  PubMed  Google Scholar 

  • Dolatabadian A, Sanavy SAMM, Chashmi NA (2008) The effects of foliar application of ascorbic acid (vitamin C) on antioxidant enzymes activities, lipid peroxidation and proline accumulation of Canola (Brassica napus L.) under conditions of salt stress. J Agron Crop Sci 194:206–213

    Article  CAS  Google Scholar 

  • Doorenbos J, Kassam AH (1986) Yield response to water, irrigation and drainage. Paper 33. FAO, Rome, Italy

  • Epron D, Dreyer E (1991) Effects of severe dehydration on leaf photosynthesis in Quercus petraea (Matt.) Liebl.: photosystem II efficiency, photochemical and nonphotochemical fluorescence quenching and electrolyte leakage. Tree Physiol 10:273–284

    Article  Google Scholar 

  • Ferrara A, Lovelli S, Di Tommaso T, Perniola M (2011) Flowering, growth and fruit setting in greenhouse bell pepper under water stress. J Agron 10:12–19

    Article  Google Scholar 

  • Flexas J, Escalona JM, Medrano H (1999) Water stress induces different levels of photosynthesis and electron transport rate regulation in grapevines. Plant Cell Environ 22:39–48

    Article  Google Scholar 

  • González-Dugo V, Orgaz F, Fereres E (2007) Responses of pepper to deficit irrigation for paprika production. Sci Hortic 114:77–82

    Article  Google Scholar 

  • Havaux M (1992) Stress tolerance of photosystem II in vivo. Antagonistic effects of water, heat and photoinhibition stresses. Plant Physiol 100:424–432

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Hoffmann A, Noga G, Hunsche M (2015) High blue light improves acclimation and photosynthetic recovery of pepper plants exposed to UV stress. Environ Exp Bot 109:254–263

    Article  CAS  Google Scholar 

  • Hogewoning SW, Douwstra P, Trouwborst G, van Ieperen W, Harbinson J (2010a) An artificial solar spectrum substantially alters plant development compared with usual climate room irradiance spectra. J Exp Bot 61:1267–1276

    Article  CAS  PubMed  Google Scholar 

  • Hogewoning SW, Trouwborst G, Maljaars H, Poorter H, van Ieperen W, Harbinson J (2010b) Blue light dose-responses of leaf photosynthesis, morphology, and chemical composition of Cucumis sativus grown under different combinations of red and blue light. J Exp Bot 61:3107–3117

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Holden M (1976) Chlorophylls. In: Goodwin TW (ed) Chemistry and biochemistry of plant pigments, 2nd edn. Academic Press, London, pp 1–37

    Google Scholar 

  • Krall JP, Edwards GE (1992) Relationship between photosystem II activity and CO 2 fixation in leaves. Physiol Plant 86:180–187

    Article  CAS  Google Scholar 

  • Kulkarni M, Phalke S (2009) Evaluating variability of root size system and its constitutive traits in hot pepper (Capsicum annum L.) under water stress. Sci Hortic 120:159–166

    Article  Google Scholar 

  • Lawlor DW, Cornic G (2002) Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant Cell Environ 25:275–294

    Article  CAS  PubMed  Google Scholar 

  • Lichtenthaler HK (1984) Differences in morphology and chemical composition of leaves grown at different light intensities and qualities. In: Baker NR, Davies WJ, Ong KC (eds) Control of leaf growth. Cambridge University Press, Cambridge, pp 201–222

    Google Scholar 

  • Lichtenthaler HK (1996) Vegetation stress: an introduction to the stress concept in plants. J Plant Physiol 148:4–14

    Article  CAS  Google Scholar 

  • Lichtenthaler HK, Miehé JA (1997) Fluorescence imaging as a diagnostic tool for plant stress. Trends Plant Sci 2:316–320

    Article  Google Scholar 

  • Lichtenthaler HK, Babani F, Navrátil M, Buschmann C (2013) Chlorophyll fluorescence kinetics, photosynthetic activity, and pigment composition of blue-shade and half-shade leaves as compared to sun and shade leaves of different trees. Photosynth Res 117:355–366

    Article  CAS  PubMed  Google Scholar 

  • Loreto F, Tsonev T, Centritto M (2009) The impact of blue light on leaf mesophyll conductance. J Exp Bot 60:2283–2290

    Article  CAS  PubMed  Google Scholar 

  • Massa GD, Kim HH, Wheeler RM, Mitchell CA (2008) Plant productivity in response to LED lighting. HortScience 43:1951–1956

    Google Scholar 

  • Maxwell K, Johnson GN (2000) Chlorophyll fluorescence—a practical guide. J Exp Bot 51:659–668

    Article  CAS  PubMed  Google Scholar 

  • Murakami K, Matsuda R, Fujiwara K (2014) Light-induced systemic regulation of photosynthesis in primary and trifoliate leaves of Phaseolus vulgaris: effects of photosynthetic photon flux density (PPFD) versus spectrum. Plant Biology 16:16–21

    Article  CAS  Google Scholar 

  • Muraoka H, Tang Y, Koizumi H, Washitani I (2002) Effects of light and soil water availability on leaf photosynthesis and growth of Arisaema heterophyllum, a riparian forest understorey plant. J Plant Res 115:419–427

    Article  CAS  PubMed  Google Scholar 

  • Murchie EH, Lawson T (2013) Chlorophyll fluorescence analysis: a guide to good practice and understanding some new applications. J Exp Bot 64:3983–3998

    Article  CAS  PubMed  Google Scholar 

  • Quick WP, Stitt M (1989) An examination of factors contributing to non-photochemical quenching of chlorophyll fluorescence in barley leaves. Biochim Biophys Acta 977:287–296

    Article  CAS  Google Scholar 

  • Ralph PJ, Gademann R (2005) Rapid light curves: a powerful tool to assess photosynthetic activity. Aquat Bot 82:222–237

    Article  CAS  Google Scholar 

  • Sarijeva G, Knapp M, Lichtenthaler HK (2007) Differences in photosynthetic activity, chlorophyll and carotenoid levels, and in chlorophyll fluorescence parameters in green sun and shade leaves of Ginko and Fagus. J Plant Physiol 164:950–955

    Article  CAS  PubMed  Google Scholar 

  • Savvides A, Fanourakis D, van Ieperen W (2012) Co-ordination of hydraulic and stomatal conductances across light qualities in cucumber leaves. J Exp Bot 63:1135–1143

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Schuerger AC, Brown CS, Stryjewski EC (1997) Anatomical features of pepper plants (Capsicum annuum L.) grown under red light-emitting diodes supplemented with blue or far-red light. Ann Bot 79:273–282

    Article  CAS  PubMed  Google Scholar 

  • Sellaro R, Crepy M, Trupkin SA, Karayekov E, Buchovsky AS, Rossi C, Casal JJ (2010) Cryptochrome as a sensor of the blue/green ratio of natural radiation in Arabidopsis. Plant Physiol 154:401–409

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Sezen SM, Yazar A, Eker S (2006) Effect of drip irrigation regimes on yield and quality of field grown bell pepper. Agr Water Manage 81:115–131

    Article  Google Scholar 

  • Smittle DA, Lamar Dickens W, Stansell JR (1994) Irrigation regimes affect yield and water use by bell pepper. J Am Soc Hortic Sci 119:936–939

    Google Scholar 

  • Strobl A, Türk R (1990) Untersuchungen zum Chlorophyllgehalt einiger subalpiner Flechtenarten. Phyton Ann Rei Bot A 30:247–264

    CAS  Google Scholar 

  • Sziderics AH, Oufir M, Trognitz F, Kopecky D, Matusikova I, Hausman JF, Wilhelm E (2010) Organ-specific defence strategies of pepper (Capsicum annuum L.) during early phase of water deficit. Plant Cell Rep 29:295–305

    Article  CAS  PubMed  Google Scholar 

  • Terashima I, Fujita T, Inoue T, Chow WS, Oguchi R (2009) Green light drives leaf photosynthesis more efficiently than red light in strong white light: revisiting the enigmatic question of why leaves are green. Plant Cell Physiol 50:684–697

    Article  CAS  PubMed  Google Scholar 

  • Terfa MT, Solhaug KA, Gislerod HR, Olsen JE, Torre S (2013) A high proportion of blue light increases the photosynthesis capacity and leaf formation rate of Rosa x hybrida but does not affect time to flower opening. Physiol Plantarum 148:146–159

    Article  CAS  Google Scholar 

  • Wada M (2013) Chloroplast movement. Plant Sci 210:177–182

    Article  CAS  PubMed  Google Scholar 

  • Walters RG (2005) Towards an understanding of photosynthetic acclimation. J Exp Bot 56:435–447

    Article  CAS  PubMed  Google Scholar 

  • Walters RG, Horton P (1991) Resolution of components of noon-photochemical chlorophyll fluorescence quenching in barley leaves. Photosynth Res 27:121–133

    Article  CAS  PubMed  Google Scholar 

  • Xiaoying L, Shirong G, Taotao C, Zhigang X, Tezuka T (2012) Regulation of the growth and photosynthesis of cherry tomato seedlings by different light irradiations of light emitting diodes (LED). Afr J Biotechnol 11:6169–6177

    Google Scholar 

  • Zeiger E, Field C (1982) Photocontrol of the functional coupling between photosynthesis and stomatal conductance in the intact leaf. Plant Physiol 70:370–375

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Zhang T, Maruhnich SA, Folta KM (2011) Green light induces shade avoidance symptoms. Plant Physiol 157:1528–1536

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Ziska LH, Teramura AH, Sullivan JH (1992) Physiological sensitivity of plants along an elevational gradient to UV-B radiation. Am J Bot 79:863–871

    Article  Google Scholar 

Download references

Acknowledgments

The authors thank Mr. Toshihiko Oishi, Ushio Europe B. V. (The Netherlands), and the group of technical engineers from Ushio Lighting Inc. (Japan) for developing and making the LED panels available for this study. We are grateful to Prof. Dr. Uwe Rascher, Institute of Bio- and Geoscience (IBG-2), Jülich Research Center, for loaning the spectroradiometer. Many thanks to Libeth Schwager, INRES Horticultural Science, for her support in the laboratory and to Elif Köllhofer for her assistance during the experimental phase. Finally, we acknowledge the Theodor-Brinkmann-Graduate School (Faculty of Agriculture, University of Bonn) for providing a scholarship to the first author. We also appreciate the critical-constructive comments of the anonymous reviewers.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mauricio Hunsche.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 37 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hoffmann, A.M., Noga, G. & Hunsche, M. Acclimations to light quality on plant and leaf level affect the vulnerability of pepper (Capsicum annuum L.) to water deficit. J Plant Res 128, 295–306 (2015). https://doi.org/10.1007/s10265-014-0698-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10265-014-0698-z

Keywords

Navigation