Skip to main content
Log in

QTLs for chlorophyll and chlorophyll fluorescence parameters in barley under post-flowering drought

  • Published:
Euphytica Aims and scope Submit manuscript

Abstract

Drought is one of the major factors limiting barley yields in many developing countries worldwide. The identification of molecular markers linked to genes controlling drought tolerance in barley is one way to improve breeding efficiency. In this study, we analyzed the quantitative trait loci (QTL) controlling chlorophyll content and chlorophyll fluorescence in 194 recombinant inbred lines (RILs) developed from the cross between the cultivar ‘Arta’ and Hordeum spontaneum 41-1. Five traits, chlorophyll content, and four chlorophyll fluorescence parameters, namely initial fluorescence (Fo), maximum fluorescence (Fm), variable fluorescence (Fv), and maximum quantum efficiency of PSII (Fv/Fm) which are related to the activity of the photosynthetic apparatus, were measured under well-watered and drought stress conditions at post-flowering stage. QTL analysis identified a total of nine and five genomic regions, under well-watered and drought stress conditions, respectively, that were significantly associated with the expression of the five target traits at post-flowering stage. No common QTL was detected except one for chlorophyll content, which was identified in both growth conditions, demonstrating that the genetic control of the expression of the traits related to photosynthesis differed under different water conditions. A QTL for Fv/Fm, which is related to the drought tolerance of photosynthesis was identified on chromosome 2H at 116 cM in the linkage map under drought stress. This QTL alone explained more than 15% of phenotypic variance of maximum quantum yield of PSII, and was also associated with the expression of four other traits. In addition, another QTL for Fv/Fm was also located on the same chromosome (2H) but at 135.7 cM explaining around 9% of the phenotypic variance under drought conditions. The result presented here suggest that two major loci, located on chromosome 2H, are involved in the development of functional chloroplast at post-flowering stage for drought tolerance of photosynthesis in barley under drought stress. If validated in other populations, chlorophyll fluorescence parameters could be used as selection criteria for drought tolerance.

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

Similar content being viewed by others

References

  • Angelopoulous K, Dichio B, Xiloyannis C (1996) Inhibition of photosynthesis in olive trees (Olea europea L.) during water stress and rewatering. J Exp Bot 47:1093–1100

    Article  Google Scholar 

  • Araus JL, Hogan K (1994) Comparative leaf structure and patterns of photoinhibition of the neotropical palms. Scheelea zonensis and Socratea durissima growing in clearing and forest understory during the dry season in Panama. Am J Bot 81:726–738

    Article  Google Scholar 

  • Araus JL, Amaro T, Voltas J, Nakkoul H, Nachit MM (1998) Chlorophyll fluorescence as a selection criterion for grain yield in durum wheat under Mediterranean conditions. Field Crop Res 55:209–223

    Article  Google Scholar 

  • Arnon DI (1949) Copper enzymes in isolated chloroplasts polyphenoloxidase in Beta. vulgaris. Plant Physiol 24:1–15

    Article  PubMed  CAS  Google Scholar 

  • Baenziger M, Edmeades GO, Lafitte HR (1999) Selection for drought tolerance increases maize yields across a range of nitrogen levels. Crop Sci 39:1035–1040

    Article  Google Scholar 

  • Baker NR, Bowyer J (1994) Photoinhibition of photosynthesis: from molecular mechanisms to the field. BIOS scientific publishers Ltd, Oxford. UK

    Google Scholar 

  • Baker NR, Horton P (1987) Chlorophyll fluorescence quenching during photoinhibition. In: Kyle DJ, Osmond CB, Arntzen CJ (eds) Photoinhibition. Elsevier Science Publishers, Amsterdam, pp 145–168

    Google Scholar 

  • Bassam BJ, Caetano-Anolles G, Gresshoff PM (1991) Fast and sensitivity silver staining of DNA in polyacrilamide gel. Anal Biochem 196:80–83

    Article  PubMed  CAS  Google Scholar 

  • Baum M, Grando S, Backes G, Jahoor A, Sabbagh A, Ceccarelli S (2003) QTLs for agronomic traits in the Mediterranean environment identified in recombinant inbred lines of the cross ‘Arta’ × H. spontaneum 41-1. Theor Appl Genet 107:1215–1225

    Article  PubMed  CAS  Google Scholar 

  • Benbella M, Paulsen GM (1998) Efficacy of treatments for delaying senescence of wheat leaves: II. Senescenece and grain yield under field conditions. Agron J 90:332–338

    Article  Google Scholar 

  • Blum A (1998) Improving wheat grain filling under stress by stem reserve mobilization. Euphytica 100:77–83

    Article  Google Scholar 

  • Bolhar-Nordenkampf HR, Long SP, Baker NR, Öquist G, Schreiber U, Lechner EG (1989) Chlorophyll fluorescence as a probe of the photosynthetic competence of leaves in the field: a review of current instrumentation. Funct Ecol 3:497–514

    Article  Google Scholar 

  • Borrell AK, Hammer GL, Henzell RG (2000) Does maintaining green leaf area in sorghum improve yield under drought? II. Dry matter production and yield. Crop Sci 40:1037–1048

    Article  Google Scholar 

  • Ceccarelli S (1994) Specific adaptation and breeding for marginal conditions. Euphytica 77:205–219

    Article  Google Scholar 

  • Ceccarelli S, Grando S, Baum M, Udupa SM (2004) Breeding for drought resistance in a changing climate. In: Rao SC, Ryan J (eds) Challenges and strategies for dryland agriculture. CSSA Spec Publ. 32. ASA and CSSA, Madison, WI, pp 167–190

    Google Scholar 

  • Ceccarelli S, Grando S, Baum M (2007) Participatory plant breeding in water-limited environments. Environ Exp Agric 43:411–435

    Article  Google Scholar 

  • Cellier F, Conejero G, Breitler JC, Casse F (1998) Molecular and physiological responses to water deficit in drought-tolerant and drought-sensitive lines of sunflowers. Accumulation of dehydrin transcripts correlates with tolerance. Plant Physiol 116:319–328

    Article  PubMed  CAS  Google Scholar 

  • Clark AJ, Landolt W, Bucher JB, Strasser RJ (2000) Beech (Fagus Sylvatica) response to ozone exposure assessed with a chlorophyll fluorescence performance index. Environ Pollut 109:501–507

    Article  PubMed  CAS  Google Scholar 

  • Cochard H, Coll L, Roux XL, Améglio T (2002) Unraveling the effects of plant hydraulics on stomatal closure during water stress in walnut. Plant Physiol 128:282–290

    Article  PubMed  CAS  Google Scholar 

  • Courtois B, McLaren G, Sinha PK, Prasad K, Yadav R, Shen L (2000) Mapping QTL associated with drought avoidance in upland rice. Mol Breed 6:55–66

    Article  CAS  Google Scholar 

  • Dau H (1994) Molecular mechanisms and quantitative models of variable Photosystem II fluorescence. Photochem Photobiol 60:1–23

    Article  CAS  Google Scholar 

  • Doorenbos J, Pruit WO (1977) Guidelines for predicting crop water requirements. FAO irrigation and drainage paper no. 24. Food Agric Org UN, Rome

  • Fracheboud Y, Jompuk C, Ribaut JM, Stamp P, Leipner J (2004) Genetic analysis of cold-tolerance of photosynthesis in maize. Plant Mol Biol 56:241–253

    Article  PubMed  CAS  Google Scholar 

  • Graan T, Boyer JS (1990) Very high CO2 partially restores photosynthesis in sunflower at low water potentials. Planta 181:378–384

    Article  CAS  Google Scholar 

  • Grando S, von Bothmer R, Ceccarelli S (2001) Genetic diversity of barley: use of locally adapted germplasm to enhance yield and yield stability of barley in dry areas. In: Cooper HD, Spillane C, Hodgink T (eds) Broadening the genetic base of crop production. CABI/FAO/IPGRI, pp 351–372

  • Grando S, Baum M, Ceccarelli S, Goodchild A, Jaby El-Haramein F, Jahoor A, Backes G (2005) QTLs for straw quality characteristics identified in recombinant inbred lines of a Hordeum vulgare and H. spontaneum cross in a Mediterranean environment. Theor Appl Genet 110:688–695

    Article  PubMed  CAS  Google Scholar 

  • Greaves JA, Wilson JM (1987) Chlorophyll fluorescence analysis—an aid to plant breeders. Biologist 34(4):209–214

    Google Scholar 

  • Guo P, Al-Khatib K (2003) Temperature effects on germination and growth of redroot pigweed (Amaranthus retroflexus), Palmer amaranth (A. almery), and common waterhemp (A. rudis). Weed Sci 51:869–875

    Article  CAS  Google Scholar 

  • Guo P, Li M (1996) Studies on photosynthetic characteristics in rice hybrid progenies and their parents I. chlorophyll content, chlorophyll-protein complex and chlorophyll fluorescence kinetics. J Tropic Subtropic Bot 4(4):60–65

    Google Scholar 

  • Guo P, Li R (2000) Effects of high nocturnal temperature on photosynthetic organization in rice leaves. Acta Botanica Sinica 42(7):13–18

    Google Scholar 

  • Hakam N, Khanizadeh S, DeEll JR, Richer C (2000) Assessing chilling tolerance in roses using chlorophyll fluorescence. HortScience 35:184–186

    Google Scholar 

  • Haussmann BIG, Mahalakshmi V, Reddy BVS, Seetharama N, Hash CT, Geiger HH (2002) QTL mapping of stay-green in two sorghum recombinant inbred populations. Theor Appl Genet 106:133–142

    PubMed  CAS  Google Scholar 

  • He JX, Wang J, Liang HG (1995) Effect of water stress on photochemical function and protein metabolism of photosystem II in wheat leaves. Physiol Plant 93:771–777

    Article  CAS  Google Scholar 

  • Hong SS, Xu DQ (1999) Light-induced increase in chlorophyll fluorescence Fo level and the reversible inactivation of PSII reaction centers in soybean leaves. Photosyn Res 61:269–280

    Article  CAS  Google Scholar 

  • Horton P, Ruban AV, Walters RG (1996) Regulation of light harvesting in green plants. Ann Rev Plant Physiol Mol Biol 47:655–684

    Article  CAS  Google Scholar 

  • Kosambi DD (1944) The estimation of map distance from recombination values. Ann Eugen 12:172–175

    Google Scholar 

  • Krause GH, Weiss E (1991) Chlorophyll fluorescence and photosynthesis: the basics. Ann Rev Plant Physiol 42:313–349

    Article  CAS  Google Scholar 

  • Li R, Guo P, Baum M, Grando S, Ceccarelli S (2006) Evaluation of chlorophyll content and fluorescence parameters as indicators of drought tolerance in barley. Agric Sci China 5:751–757

    Article  CAS  Google Scholar 

  • Long SP, Humphries S, Falkowski PG (1994) Photoinhibition of photosynthesis in nature. Ann Rev Plant Physiol Plant Mol Biol 45:633–662

    Article  CAS  Google Scholar 

  • Lu C, Zhang J (1999) Effects of water stress on photosystem II photochemistry and its thermostability in wheat plants. J Exp Bot 50:1199–1206

    Article  CAS  Google Scholar 

  • Percival GC, Sheriffs CN (2002) Identification of drought-tolerance woody perennials using chlorophyll fluorescence. J Arboriculture 28:215–223

    Google Scholar 

  • Payne R, Murray D, Harding S, Baird D, Soutou D, Lane P (2003) GenStat for Windows (7th edition)—Introduction. VSN International, Oxford, England

    Google Scholar 

  • Ramsay L, Macaulay M, Degli Ivanissevich S, Maclean K, Carsle L, Fuller J, Edwards KJ, Tuvesson S, Morgante M, Massari A, Maestri E, Marmiroli N, Sjakste T, Ganal M, Powell W, Waugh R (2000) A simple sequence repeat-based linkage map of barley. Genetics 156:1997–2005

    PubMed  CAS  Google Scholar 

  • Rawson HM, Constable GA, Howe GN (1980) Carbon production of sunflower cultivars in field and well-wateredled environments. II. leaf growth. Aust J Plant Physiol 7:575–586

    Article  Google Scholar 

  • Ribaut JM, Jiang C, González-de-León D, Edmeades GO, Hoisington DA (1997) Identification of quantitative trait loci under drought conditions in tropical maize. 2. Yield components and marker-assisted selection. Theor Appl Genet 94:887–896

    Article  Google Scholar 

  • Ryan J, Estefan G, Rashid A (2001) Soil and plant analysis laboratory manual. 2nd edn. Jointly published by the Internation Center for Agricultural Research in the Dry Areas (ICARDA) and the National Agricultural Research Center (NARC), Aleppo, Syria

    Google Scholar 

  • Sacks MM, Silk WK, Burman P (1997) Effect of water stress on cortical cell division rates within the apical meristem of primary roots of maize. Plant Physiol 114:519–527

    PubMed  CAS  Google Scholar 

  • Saghai-Maroof MA, Soliman KM, Gorgensen RA, Allard RW (1984) Ribosomal DNA spacer-length polymorphism in barley: Mendelian inheritance, chromosomal location and population dynamics. Proc Natl Acad Sci USA 81:8014–8018

    Article  PubMed  CAS  Google Scholar 

  • Schreiber U, Bilger W, Neubauer C (1994) Chlorophyll fluorescence as a non-intrusive indicator for rapid assessment of in vivo photosynthesis. In: Schulze ED, Caldwell MM (eds) Ecophysiology of photosynthesis. Ecological studies, Vol 100. Springer, Berlin Heidelberg New York, pp 49–70

    Google Scholar 

  • Stam P, Van Ooijen JW (1995) JoinMap version 2.0: software for the calculation of genetic linkage maps. CPRO-DLO, Wageningen

    Google Scholar 

  • Van Ooijen JW (2004) MapQTL 5.0: software for the mapping of quantitative trait loci in experimental populations. Kyazma B.V., Wageningen, Netherlands

    Google Scholar 

  • Verma V, Foulkes MJ, Worland AJ, Sylvester-Bradley R, Caligari PDS, Snape JW (2004) Mapping quantitative trait loci for flag leaf senescence as a yield determinant in winter wheat under optimal and drought-stressed environments. Euphytica 135:255–263

    Article  CAS  Google Scholar 

  • Yamada M, Hidaka T, Fukamachi H (1996) Heat tolerance in leaves of tropical fruit crops as measured by chlorophyll fluorescence. Sci Hortic 67:3948

    Article  Google Scholar 

  • Zabeau M, Vos P (1993) Selective restriction fragment amplification: a general method for DNA fingerprinting. Eur Pat App 92402629.7 (Publ Number 0 534858 A1)

Download references

Acknowledgements

The authors’ research was supported by grants to ICARDA from the German Federal Ministry of Economic Cooperation and Development (BMZ, Bonn, Germany) under the project “Exploration of Genetic Resources Collections at ICARDA for Adaptation to Climate Change: Identification and Utilization of Sources of Stress Tolerance”, the Generation Challenge Program and National Natural Science Foundation of China (30640045). We would like to acknowledge Dr. M. Singh for help in biometric analysis, and Dr. A. Brueggeman for soil-water analysis.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Michael Baum.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Guo, P., Baum, M., Varshney, R.K. et al. QTLs for chlorophyll and chlorophyll fluorescence parameters in barley under post-flowering drought. Euphytica 163, 203–214 (2008). https://doi.org/10.1007/s10681-007-9629-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10681-007-9629-6

Keywords

Navigation