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Evaluation of wild Arachis species for abiotic stress tolerance: I. Thermal stress and leaf water relations

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Abstract

The Indian groundnut cultivars have a narrow genetic base. Hence, it was of interest to investigate the genetic variability among wild Arachis species and their accessions for tolerance to thermal stress. A wide variation was observed in leaf morphological characters such as colour, shape, hairiness, length and width and thickness (SLA). The temperature and time required for 50% leaf injury was worked out with limited number of genotypes and was found to be 54°C for 50 min. Among 36 genotypes (having SLA in the range of 66 and 161 cm2 g−1) screened, the inherent potential for cold as well as heat tolerance in terms of relative leaf injury (RI) was observed. Thus, based on RI-values, A. glabrata 11824 and A. paraguariensis 12042 were identified as heat-tolerant and cold-tolerant genotypes, respectively while A. appresipila 11786 was found to be susceptible to both heat and cold. Correlation between SLA and RI values for heat (r = 0.38, P < 0.05) and cold (r = 0.52, P < 0.05) tolerance was positive, indicating that thicker the leaf the lower the injury or higher the tolerance. Among six species and 13 accessions, comprising both heat-tolerant and heat- susceptible genotypes, the concentrations of various leaf chemical constituents such as total protein, phenols, sugars, reducing sugar, amino acids, proline, epicuticular wax load and chlorophyll varied significantly. The epicuticular wax load ranged between 1.1 and 2.5 mg dm2 among 13 A.glabrata accessions. These accessions were categorized into two groups, i.e. high-wax (range: 2.0–2.5 mg dm2) and low-wax types (range: 1.1–1.6 mg dm2). The high-wax type showed a higher diffusion resistance (dr) as compared to low-wax type; though the transpiration rate (tr) in high-wax type was moderate (between 9.5 and 11.6 μg cm−2 s−1). Genetic variability in parameters such as canopy temperature, dr and tr was also distinct. The fully turgid leaves with relative water content ≥91%, showed leaf water potential (ψleaf) between −0.7 and −1.2 MPa. Results indicated that the plants with thicker leaves are better protected from heat injuries. Further, epicuticular wax load seems to help in maintaining stomatal regulation and leaf water relations, thus affording adaptation to wild Arachis species to thrive under water-limited environments. The sources of tolerance, as identified in this study, could be utilized to improve thermal tolerance of the groundnut cultivars by intra-specific hybridization, following either conventional breeding using embryo rescue techniques, if required or utilizing biotechnological tools.

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References

  • Arnon DI (1949) Copper enzymes in intact chloroplast. Polyphenoxidase in Beta vulgaris. Plant Physiol 24:1–15

    PubMed  CAS  Google Scholar 

  • Ashwell G (1957) Colorimetric analysis of sugars. In: Colowick SP, Kaplan NO (eds) Methods of enzymology, vol 3. Academic Press, New York, pp 73–105

    Google Scholar 

  • Ballentine R (1957) Determination of total nitrogen and ammonia. In: Clowick SP, Kaplan NO (eds) Methods of enzymology, vol 3. Academic Press, New York, pp 984–995

    Google Scholar 

  • Barrs HD, Weatherley PE (1962) A re-examination of the relative turgidity technique for estimating water deficit in leaves. Aust J Biol Sci 15:413–428

    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 

  • Bhagat NR. Dayal D, Acharya D (1992) Performance of Spanish peanuts during winter-summer season at two locations in India. Trop Agri (Trinad.) 69:93–95

    Google Scholar 

  • Bhagat NR, Ahmed T, Lalwani HB, Patil SA, Patra GJ, Acharya D (1988) Screening of bunch peanut (A. hypogaea) germplasm for cold tolerance in India. Trop Agri (Trinad) 65:109–112

    Google Scholar 

  • Bray HG, Thrope WV (1954) Analysis of phenolic compounds of interest in metabolism. In: Glick D (ed) Methods of biochemical analysis, vol 1. Interscience Publishers Inc., New York, pp 27–52

  • Chaisomponpan N, Li PH, Davis DW, Markhart AH III (1990) Photosynthetic response to heat stress in common bean genotype differing in heat acclimation potential. Crop Sci 30:100–104

    Article  Google Scholar 

  • Chen HH, Shen ZY, Li PH (1982) Adaptability of crop plants to high temperature. Crop Sci 22:719–725

    Article  Google Scholar 

  • Cox FR (1979) Effect of temperature on peanut vegetative and reproductive growth. Peanut Sci 6:14–17

    Article  Google Scholar 

  • Craufurd PQ, Vara Prasad PV, Kakani VG, Wheeler TR (2000) Tolerance to high soil and air temperature in peanut. In: Book of Abstracts, 3rd International Crop Science Congress, 17–22 August 2000. European Society for Agronomy, Hamburg Germany, p 63

  • Ebercon A, Blum A, Jordan WR (1977) A rapid calorimetric method for epicuticular wax content of sorghum leaves. Crop Sci 17:179–180

    Article  Google Scholar 

  • Gomez KA, Gomez AA (1984) Statistical Procedures for Agricultural Research. Wiley, New York

    Google Scholar 

  • Hossain MM, Takeda H, Senbok T (1995) Improved method of membrane thermostabiliity for screening heat resistance and sensitive varieties in cabbage. JIRCAS J 2:19–27

    Google Scholar 

  • Howarth CJ (1991) Molecular responses of plants to an increased incidence of heat shock. Plant Cell Env 14:831–841

    Article  CAS  Google Scholar 

  • Howarth CJ, Pollock CJ, Pea Cock JM (1997) Development of laboratory-based methods for assessing seedling thermostability in pearl millet. New Phytol 137:129–139

    Article  Google Scholar 

  • Howarth CJ, Cavan GP, Skot KP, Layton RWH, Witcombe JR (1994) Mapping QTLs for heat tolerance in pearl millet. In: Witcombe JR, Duncan RR (eds) The use of molecular marker in sorghum and pearl millet, breeding for developing countries. Overseas development administration, London, pp 80–85

    Google Scholar 

  • ICRISAT (1992) Descriptores for groundnut. IBPGR/ICRISAT, Rome. pp 125, Printed at ICRISAT, Patancheru, India

  • Joshi YC, Nautiyal PC, Ravindra V, Dwivedi RS (1988) Water relations in two cultivars of groundnut (Arachis hypogaea L.) under soil water-deficit. Trop Agric (Trinadad) 65:182–184

    Google Scholar 

  • Joshi YC, Nautiyal PC, Ravindra V (1996) Screening for cold tolerance and osmoconditioning to enhance germination of groundnut in suboptimal temperature. Trop Sci 36:224–228

    Google Scholar 

  • Ketring DL (1995) Evaluation of peanut genotypes for membrane thermostability. Peanut Sci 12:25–32

    Google Scholar 

  • Kripling EB (1967) Measurement of leaf water potential by the dye method. Ecology 48:1038–1041

    Article  Google Scholar 

  • Larkindale J, Bingru H (2004) Changes in lipid composition and saturation levels and roots for heat-stressed and heat-acclimated creeping bentgrass (Agrostis stolonifera). Environ Exp Bot 51:57–67

    Article  CAS  Google Scholar 

  • Liu CJ, Witcome JR, Pittaway TS, Nash N, Hash CT, Busso CS, Gale MD (1994) An RFLP-based gene map of pearl millet. Theor Appl Genet 89:481–487

    CAS  Google Scholar 

  • Nautiyal PC, Bhanushali TB, Prakash V (2002a) Performance of groundnut germplasm at high temperatures during reproductive phase in Rajasthan, India. Inter Arachis Newslett 22:18–22

    Google Scholar 

  • Nautiyal PC, Shono M, Egawa Y (2005) Enhanced thermotolerance of the vegetative part of MT-sHSP transgenic tomato line. Sci Hort 105:393–409

    Article  Google Scholar 

  • Nautiyal PC, Rachaputi NR, Joshi YC (2002b) Moisture-deficit induced changes in leaf water content, leaf carbon exchange rate and biomass production in groundnut cultivars differing in specific leaf area. Field Crop Res 74:67–79

    Article  Google Scholar 

  • Nautiyal PC, Ravindra V, Joshi YC (1995) Gas exchange and water relations in two peanut cultivars of different drought tolerance. Biol Plant 37:371–374

    Article  Google Scholar 

  • Nishiyam Y, Los D, Murata N (1999) PsbU, a protein associated with PS II is required for the acqussition of cellular thermotolerance in Synechococcus species, PCC 7002. Plant Physiol 120:301–308

    Article  Google Scholar 

  • Raison JK, Berry JA, Armond PA, Pike CS (1980) Membrane proteins in relation to the adaptation of plants to temperature stress. In: Turner NC, Kramer PJ (eds) Adaptation of plants to water and high temperature stress. Wiley, New York, pp 261–273

    Google Scholar 

  • Saadalla MM, Shanahan JF, Quick JS (1990) Heat tolerance in winter wheat: I. Hardening and genetic effects on membrane thermostability. Crop Sci 30:1243–1247

    Article  Google Scholar 

  • Samdur MY, Manivel P, Jain VK, Chikani BM, Gor HK, Desai S, Misra JB (2003) Genotypic differences and water deficit-induced enhancement in epicuticular wax load in peanut. Crop Sci 43:1294–1299

    Article  Google Scholar 

  • Santoro MM, Liu Y, Khan SMA, Hou LX, Bolen DW (1992) Increase thermal stability of proteins in the presence of naturally occurring osmolytes. Biochemistry 31:5278–5283

    Article  PubMed  CAS  Google Scholar 

  • Shi WM, Muramoto Y, Ueda A, Takabe T (2001) Cloning of peroximal ascorbate gene from barley and enhanced thermotolerance by overexpressing in Arabidopsis thaliana. Gene 273:23–27

    Article  PubMed  CAS  Google Scholar 

  • Singleton JA, Pattee HE (1997) Effect of cold and heat stress on the chemistry and cell structure of peanut seeds. Peanut Sci 24:32–37

    Article  CAS  Google Scholar 

  • Spies JR (1957) Calorimetric procedure for amino acid. In: Clowick SP, Kaplin NO (eds) Methods of enzymology, vol 3. Academic Press, New York, pp 467–477

    Google Scholar 

  • Srinivasan A, Takeda H, Senboku T (1996) Heat tolerence in food legumes as evaluated by cell membrane thermostability and chlorophyll fluorescence techniques. Euphytica 88:35–45

    Article  Google Scholar 

  • Sung D-Y, Kaplan F, Kil-Jae L, Guy CL (2003) Acquired tolerance to temperature extremes. Tren Plant Sci 8:179–187

    Article  CAS  Google Scholar 

  • Suss KH, Yordanov IT (1986) Biosynthetic causes of in vivo acquired thermotolerance of photosynthetic light reactions and metabolic responses of chloroplasts to heat stress. Plant Physiol 81:192–199

    Article  PubMed  CAS  Google Scholar 

  • Talwar HS, Takeda H, Yashima S, Senboku T (1999) Growth and photosynthetic responses of groundnut genotypes to high temperature. Crop Sci 39:460–466

    Article  Google Scholar 

  • Vakharia DN, Davaria RL, Parameswaran M (1993) Change in cuticular wax content in leaves of two groundnut cultivars during and after relief of drought. Plant Physiol Biochem 20:96–98

    Google Scholar 

  • Vara Prasad PV, Craufurd PQ, Summerfield RJ (1999a) Fruit number in relation to pollen production and viability in groundnut exposed to short episodes of heat stress. Ann Bot (Lond) 84:381–386

    Article  Google Scholar 

  • Vara Prasad PV, Craufurd PQ, Summerfield RJ (1999b) Sensitivity of groundnut to timing of heat stress during reproductive development. Crop Sci 39:1352–1357

    Article  Google Scholar 

  • Vara Prasad PV, Craufurd PQ, Summerfield RJ, Wheeler TR (2000) Effects of short episodes of heat stress on flower production and fruit-set in peanut (Arachis hypogaea L.). J Exp Bot 51:777–784

    Article  Google Scholar 

  • Vigh L, Los DA, Horvath I, Murata N (1993) The primary signal in the biological perception of temperature. Pd Catalysed hydrogenation of the membrane lipids simulation. The expression of the des A gene in Synexcho cystis PC 6803. Proc Natl Acad Sci 90:9090–9094

    Article  PubMed  CAS  Google Scholar 

  • Vigh L, Gombos Z, Horvath I, Joo F (1989) Saturation of membrane lipids by hydrogenation induces thermal stability in chloroplast inhibiting the heat development simulation of photosystem I mediated electron transport. Biochem Biophys Acta 979:361–364

    Article  CAS  Google Scholar 

  • Wood IM (1968) The effect of temperature at early flowering on the growth and development of peanut. Aus J Agric Res 19:241–251

    Article  Google Scholar 

Download references

Acknowledgements

Work was conducted in a NATP-CGP Project No. 401 on “Physiological Studies on High-Temperature Tolerance in Groundnut”. The financial assistance from National Agriculture Technology Project (ICAR), New Delhi, is highly acknowledged. We thank Dr J B Misra, Principal Scientist, Biochemistry, NRCG, for critically going through the manuscript and suggesting the necessary corrections. This work is dedicated to the second author, Dr. K. Rajgopal, Senior Scientist, who demised on 16th July 2006 due to cancer at the age of fifty-one.

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Correspondence to P. C. Nautiyal.

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Nautiyal, P.C., Rajgopal, K., Zala, P.V. et al. Evaluation of wild Arachis species for abiotic stress tolerance: I. Thermal stress and leaf water relations. Euphytica 159, 43–57 (2008). https://doi.org/10.1007/s10681-007-9455-x

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  • DOI: https://doi.org/10.1007/s10681-007-9455-x

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