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Plant function and evolutionary biology
RESEARCH ARTICLE

Lower soil moisture threshold for transpiration decline under water deficit correlates with lower canopy conductance and higher transpiration efficiency in drought-tolerant cowpea

Nouhoun Belko A D , Mainassara Zaman-Allah B , Ndiaga Cisse A , Ndeye Ndack Diop A C , Gerard Zombre D , Jeffrey D. Ehlers C and Vincent Vadez B E
+ Author Affiliations
- Author Affiliations

A Centre d’Etude Régional pour l’Amélioration de l’Adaptation à la Sécheresse, BP 3320 Thiès-Escale, Sénégal.

B International Crops Research Institute for the Semiarid Tropics, Patancheru 502 324 Andhra Pradesh, India.

C Department of Botany and Plant Sciences, University of California, Riverside, CA 92 521-0124, USA.

D Laboratoire de Biologie et Physiologie Végétale, Unité de Formation et de Recherche en Science de la Vie et de la Terre (UFR-SVT), Université de Ouagadougou, 03 BP 7021 Ouagadougou 03, Burkina Faso.

E Corresponding author. Email: v.vadez@cgiar.org

Functional Plant Biology 39(4) 306-322 https://doi.org/10.1071/FP11282
Submitted: 19 December 2011  Accepted: 14 February 2012   Published: 28 March 2012

Abstract

As water availability is critical for reproduction, terminal drought tolerance may involve water-saving traits. Experiments were undertaken under different vapour pressure deficit (VPD) and water regimes (water stress (WS) and well watered (WW)) to test genotypic differences and trait relationships in the fraction of transpirable soil water (FTSW) at which transpiration declines, canopy conductance (proxied by transpiration rate (TR, g H2O cm–2 h–1)), canopy temperature depression (CTD, °C), transpiration efficiency (TE, g kg–1) and growth parameters, using 15 contrasting cowpea (Vigna unguiculata (L.) Walp.) genotypes. Under WW conditions at the vegetative and early podding stages, plant mass and leaf area were larger under low VPD, and was generally lower in tolerant than in sensitive genotypes. Several tolerant lines had lower TR under WW conditions and restricted TR more than sensitive lines under high VPD. Under WS conditions, transpiration declined at a lower FTSW in tolerant than in sensitive lines. Tolerant lines also maintained higher TR and CTD under severe stress. TE was higher in tolerant genotypes under WS conditions. Significant relationships were found between TR, and TE, CTD and FTSW under different water regimes. In summary, traits that condition how genotypes manage limited water resources discriminated between tolerant and sensitive lines. Arguably, a lower canopy conductance limits plant growth and plant water use, and allows tolerant lines to behave like unstressed plants until the soil is drier and to maintain a higher TR under severe stress, as lower TR at high VPD leads to higher TE.

Additional keywords: canopy temperature depression, drought stress, fraction of transpirable soil water, Vigna unguiculata.


References

Anyia AO, Herzog H (2004) Genotypic variability in drought performance and recovery in cowpea under controlled environment. Journal Agronomy & Crop Science 190, 151–159.
Genotypic variability in drought performance and recovery in cowpea under controlled environment.Crossref | GoogleScholarGoogle Scholar |

Ashok IS, Hussain A, Prasad TG, Kumar MU, Rao RCN, Wright GC (1999) Variation in transpiration efficiency and carbon isotope discrimination in cowpea. Australian Journal of Plant Physiology 26, 503–510.
Variation in transpiration efficiency and carbon isotope discrimination in cowpea.Crossref | GoogleScholarGoogle Scholar |

Bhatnagar-Mathur P, Devi MJ, Reddy DS, Lavanya M, Vadez V, Serraj R, Yamaguchi-Shinozaki K, Sharma KK (2007) Stress-inducible expression of At DREB1A in transgenic peanut (Arachis hypogaea L.) increases transpiration efficiency under water-limiting conditions. Plant Cell Reports 26, 2071–2082.
Stress-inducible expression of At DREB1A in transgenic peanut (Arachis hypogaea L.) increases transpiration efficiency under water-limiting conditions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtlWrtr%2FI&md5=3b03e32e49d5c81db5a11fad3592a327CAS |

Cho Y, Njiti VN, Chen Y, Lightfoot DA, Wood AJ (2003) Trigonelline concentration in field-grown soybean in response to irrigation. Plant Biology 46, 405–410.
Trigonelline concentration in field-grown soybean in response to irrigation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXjs1aktLc%3D&md5=69db36cdf7e147cb4cc729dc0d40a5e3CAS |

Condon AG, Richards RA, Rebetzke GJ, Farquhar GD (2004) Breeding for high water use efficiency. Journal of Experimental Botany 55, 2447–2460.
Breeding for high water use efficiency.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXovVOisrk%3D&md5=9fac3d5e455da4be2a073e101a3ba619CAS |

Cruz de Carvalho MH, Laffray D, Louguet P (1998) Comparison of the physiological responses of Phaseolus vulgaris and Vigna unguiculata cultivars when submitted to drought conditions. Environmental and Experimental Botany 40, 197–207.
Comparison of the physiological responses of Phaseolus vulgaris and Vigna unguiculata cultivars when submitted to drought conditions.Crossref | GoogleScholarGoogle Scholar |

Dadson RB, Hashem FM, Javaid I, Allen AL, Devine TE (2005) Effect of water stress on yield of cowpea (Vigna unguiculata (L.) Walp.) genotypes in the Delmarva region of the United States. Journal Agronomy & Crop Science 191, 210–217.
Effect of water stress on yield of cowpea (Vigna unguiculata (L.) Walp.) genotypes in the Delmarva region of the United States.Crossref | GoogleScholarGoogle Scholar |

Denmead OT, Shaw RH (1962) Availability of soil water to plants as affected by soil moisture content and meteorological conditions. Agronomy Journal 54, 385–390.
Availability of soil water to plants as affected by soil moisture content and meteorological conditions.Crossref | GoogleScholarGoogle Scholar |

Devi MJ, Sinclair TR, Vadez V, Krishnamurthy L (2009) Peanut genotypic variation in transpiration efficiency and decreased transpiration during progressive soil drying. Field Crops Research 114, 280–285.
Peanut genotypic variation in transpiration efficiency and decreased transpiration during progressive soil drying.Crossref | GoogleScholarGoogle Scholar |

Devi MJ, Sinclair TR, Vadez V (2010) Genotypic variation in peanut for transpiration response to vapor pressure deficit. Crop Science 50, 191–196.
Genotypic variation in peanut for transpiration response to vapor pressure deficit.Crossref | GoogleScholarGoogle Scholar |

Devi JM, Bhatnagar-Mathur P, Sharma KK, Serraj R, Anwar SY, Vadez V (2011) Relationships between transpiration efficiency (TE) and its surrogate traits in the rd29A:DREB1A transgenic groundnut). Journal Agronomy & Crop Science 197, 272–283.
Relationships between transpiration efficiency (TE) and its surrogate traits in the rd29A:DREB1A transgenic groundnut).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhtFCrurfJ&md5=9d3f0055f150813d24808b29a0b68934CAS |

Fletcher AL, Sinclair TR, Allen LH (2007) Transpiration responses to vapor pressure deficit in well watered ‘slow-wilting’ and commercial soybean. Environmental and Experimental Botany 61, 145–151.
Transpiration responses to vapor pressure deficit in well watered ‘slow-wilting’ and commercial soybean.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXpvF2qtb8%3D&md5=1b2e3e67ef3be017e492df6b9800c096CAS |

Gholipoor M, Prasad PVV, Mutava RN, Sinclair TR (2010) Genetic variability of transpiration response to vapor pressure deficit among sorghum genotypes. Field Crops Research 119, 85–90.
Genetic variability of transpiration response to vapor pressure deficit among sorghum genotypes.Crossref | GoogleScholarGoogle Scholar |

Gilbert ME, Zwieniecki MA, Holbrook NM (2011) Independent variation in photosynthetic capacity and stomatal conductance leads to differences in intrinsic water use efficiency in 11 soybean genotypes before and during mild drought. Journal of Experimental Botany 62, 2875–2887.
Independent variation in photosynthetic capacity and stomatal conductance leads to differences in intrinsic water use efficiency in 11 soybean genotypes before and during mild drought.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXmsVyksbY%3D&md5=f70ba68ae059a5c88e77f60afc66e4c7CAS |

Gwathmey CO, Hall AE (1992) Adaptation to midseason drought of cowpea genotypes with contrasting senescence traits. Crop Science 32, 773–778.
Adaptation to midseason drought of cowpea genotypes with contrasting senescence traits.Crossref | GoogleScholarGoogle Scholar |

Gwathmey CO, Hall AE, Madore MA (1992) Adaptive attributes of cowpea genotypes with delayed monocarpic leaf senescence. Crop Science 32, 765–772.
Adaptive attributes of cowpea genotypes with delayed monocarpic leaf senescence.Crossref | GoogleScholarGoogle Scholar |

Hall AE (2004) Breeding for adaptation to drought and heat in cowpea. European Journal of Agronomy 21, 447–454.
Breeding for adaptation to drought and heat in cowpea.Crossref | GoogleScholarGoogle Scholar |

Hall AE, Schulze ED (1980) Drought effects on transpiration and leaf water status of cowpea in controlled environments. Australian Journal of Plant Physiology 7, 141–147.
Drought effects on transpiration and leaf water status of cowpea in controlled environments.Crossref | GoogleScholarGoogle Scholar |

Hall AE, Mutters RG, Farquhar GD (1992) Genotypic and drought-induced differences in carbon isotope discrimination and gas exchange of cowpea. Crop Science 32, 1–6.
Genotypic and drought-induced differences in carbon isotope discrimination and gas exchange of cowpea.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK38XhvFWhsb4%3D&md5=36b4f19b4bb68d35249634f42a5d1657CAS |

Hall AE, Cisse N, Thiaw S, Elawad HOA, Ehlers JD, Ismail AM, Fery R, Roberts PA, Kitch LW, Murdock LL, Boukar O, Phillips RD, McWatters KH (2003) Development of cowpea cultivars and germplasm by the Bean/Cowpea CRSP. Field Crops Research 82, 103–134.
Development of cowpea cultivars and germplasm by the Bean/Cowpea CRSP.Crossref | GoogleScholarGoogle Scholar |

Hamidou F, Zombre G, Braconnier S (2007) Physiological and biochemical responses of cowpea genotypes to water stress under glasshouse and field conditions. Journal Agronomy & Crop Science 193, 229–237.
Physiological and biochemical responses of cowpea genotypes to water stress under glasshouse and field conditions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXpsF2qsrY%3D&md5=30c8f163ca3e6c5307417802e0126399CAS |

Hammer GL (2006) Pathways to prosperity: breaking the yield barrier in sorghum. Agricultural Science 19, 16–22.

Hufstetler EV, Boerma HR, Carter TE, Earl HJ (2007) Genotypic variation for three physiological traits affecting drought tolerance in soybean. Crop Science 47, 25–35.
Genotypic variation for three physiological traits affecting drought tolerance in soybean.Crossref | GoogleScholarGoogle Scholar |

Kholová J, Hash CT, Kakkera A, Kocŏvá M, Vadez V (2010a) Constitutive water conserving mechanisms are correlated with the terminal drought tolerance of pearl millet. Journal of Experimental Botany 61, 369–377.
Constitutive water conserving mechanisms are correlated with the terminal drought tolerance of pearl millet.Crossref | GoogleScholarGoogle Scholar |

Kholová J, Hash CT, Kumar LP, Yadav RS, Kocŏvá M, Vadez V (2010b) Terminal drought tolerant pearl millet (Pennisetum glaucum (L.) R. Br.) have high leaf ABA and limit transpiration at high vapor pressure deficit. Journal of Experimental Botany 61, 1431–1440.
Terminal drought tolerant pearl millet (Pennisetum glaucum (L.) R. Br.) have high leaf ABA and limit transpiration at high vapor pressure deficit.Crossref | GoogleScholarGoogle Scholar |

Krishnamurthy L, Vadez V, Devi MJ, Serraj R, Nigam SN, Sheshshayee MS, Chandra S, Aruna R (2007) Variation in transpiration efficiency and its related traits in a groundnut (Arachis hypogaea L.) mapping population. Field Crops Research 103, 189–197.
Variation in transpiration efficiency and its related traits in a groundnut (Arachis hypogaea L.) mapping population.Crossref | GoogleScholarGoogle Scholar |

Mai-Kodomi Y, Singh BB, Myers O, Yopp JH, Gibson PJ, Terao T (1999a) Two mechanisms of drought tolerance in cowpea. The Indian Journal of Genetics and Plant Breeding 59, 309–316.

Mai-Kodomi Y, Singh BB, Myers O, Yopp JH, Gibson PJ, Terao T (1999b) Inheritance of drought tolerance in cowpea. The Indian Journal of Genetics and Plant Breeding 59, 317–323.

Muchero W, Ehlers JD, Roberts PA (2008) Seedling stage drought-induced phenotypes and drought-responsive genes in diverse cowpea genotypes. Crop Science 48, 541–552.
Seedling stage drought-induced phenotypes and drought-responsive genes in diverse cowpea genotypes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXls1CmtL0%3D&md5=e8de380adb543136fa1f4fe671ebd9f0CAS |

Muchero W, Ehlers JD, Close TJ, Roberts PA (2009) Mapping QTL for drought stress-induced premature senescence and maturity in cowpea (Vigna unguiculata (L.) Walp.). Theoretical and Applied Genetics 118, 849–863.
Mapping QTL for drought stress-induced premature senescence and maturity in cowpea (Vigna unguiculata (L.) Walp.).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXis12gs7g%3D&md5=360d4c9518afa13b81daea000667bb8fCAS |

Muchow RC, Sinclair TR (1991) Water deficit effects on maize yields modeled under current and greenhouse climates. Agronomy Journal 83, 1052–1059.
Water deficit effects on maize yields modeled under current and greenhouse climates.Crossref | GoogleScholarGoogle Scholar |

Ogbonnaya CI, Sarr B, Brou C, Diouf O, Diop NN, Roy-Macauley H (2003) Selection of cowpea genotypes in hydroponics, pots, and field for drought tolerance. Crop Science 43, 1114–1120.
Selection of cowpea genotypes in hydroponics, pots, and field for drought tolerance.Crossref | GoogleScholarGoogle Scholar |

Onwugbuta-Enyi J (2004) Water balance and proximate composition in cowpea (Vigna unguiculata (L) Walp.) seedlings exposed to drought and flooding stress. Journal of Applied Sciences and Environmental Management 8, 55–57.

Padi FK (2004) Relationship between stress tolerance and grain yield stability in cowpea. The Journal of Agricultural Science 142, 431–443.
Relationship between stress tolerance and grain yield stability in cowpea.Crossref | GoogleScholarGoogle Scholar |

Purcell LC, Specht JE (2004) Physiological traits for ameliorating drought stress. In ‘Soybeans: improvements, production and uses. Agronomy monograph no. 16.’ 3rd ed. (Eds HR Boerma, JE Specht). pp. 569–520. (American Society of Agronomy and Crop Science, Society of America Soil Science: Madison).

Ratnakumar P, Vadez V (2011) Groundnut (Arachis hypogaea) genotypes tolerant to intermittent drought maintain a high harvest index and have small leaf canopy under stress. Functional Plant Biology 38, 1016–1023.
Groundnut (Arachis hypogaea) genotypes tolerant to intermittent drought maintain a high harvest index and have small leaf canopy under stress.Crossref | GoogleScholarGoogle Scholar |

Ratnakumar P, Vadez V, Nigam SN, Krishnamurthy L (2009) Assessment of transpiration efficiency in peanut (Arachis hypogaea L.) under drought using a lysimetric system. Plant Biology 11, 124–130.
Assessment of transpiration efficiency in peanut (Arachis hypogaea L.) under drought using a lysimetric system.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXlslajsrc%3D&md5=5510a34f4b6d66d18df5f8328ebba147CAS |

Ray JD, Sinclair TR (1997) Stomatal closure of maize hybrids in response to soil drying. Crop Science 37, 803–807.
Stomatal closure of maize hybrids in response to soil drying.Crossref | GoogleScholarGoogle Scholar |

Ray JD, Gesch RW, Sinclair TR, Allen LH (2002) The effect of vapor pressure deficit on maize transpiration response to a drying soil. Plant and Soil 239, 113–121.
The effect of vapor pressure deficit on maize transpiration response to a drying soil.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XktVGhtbc%3D&md5=6c487747f3dfc84310343cd96b3ae6c2CAS |

Richards RA, Watt M, Rebetzke GJ (2007) Physiological traits in cereal germplasm for sustainable agricultural systems. Euphytica 154, 409–425.
Physiological traits in cereal germplasm for sustainable agricultural systems.Crossref | GoogleScholarGoogle Scholar |

Ritchie JT (1981) Water dynamics in the soil–plant–atmosphere system. Plant and Soil 58, 81–96.
Water dynamics in the soil–plant–atmosphere system.Crossref | GoogleScholarGoogle Scholar |

Sadok W, Sinclair TR (2009) Genetic variability of transpiration response to vapor pressure deficit among soybean cultivars. Crop Science 49, 955–960.
Genetic variability of transpiration response to vapor pressure deficit among soybean cultivars.Crossref | GoogleScholarGoogle Scholar |

Sheshshayee MS, Bindumadhava H, Rachaputi NR, Prasad TG, Udayakumar M, Wright GC, Nigam SN (2006) Leaf chlorophyll concentration relates to transpiration efficiency in peanut. The Annals of Applied Biology 148, 7–15.
Leaf chlorophyll concentration relates to transpiration efficiency in peanut.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XjslWis7k%3D&md5=2535f858510b72904224d537a2080873CAS |

Sinclair TR, Ludlow MM (1986) Influence of soil water supply on the plant water balance of four tropical grain legumes. Australian Journal of Plant Physiology 13, 329–341.
Influence of soil water supply on the plant water balance of four tropical grain legumes.Crossref | GoogleScholarGoogle Scholar |

Sinclair TR, Muchow RC (2001) System analysis of plant traits to increase grain yield on limited water supplies. Agronomy Journal 93, 263–270.
System analysis of plant traits to increase grain yield on limited water supplies.Crossref | GoogleScholarGoogle Scholar |

Sinclair TR, Hammer GL, Van Oosterom EJ (2005) Potential yield and water-use efficiency benefits in sorghum from limited maximum transpiration rate. Functional Plant Biology 32, 945–952.
Potential yield and water-use efficiency benefits in sorghum from limited maximum transpiration rate.Crossref | GoogleScholarGoogle Scholar |

Sinclair TR, Messina CD, Beatty A, Samples M (2010) Assessment across the United States of the benefits of altered soybean drought traits. Agronomy Journal 102, 475–482.
Assessment across the United States of the benefits of altered soybean drought traits.Crossref | GoogleScholarGoogle Scholar |

Singh BB, Matsui T (2002) Cowpea varieties for drought tolerance. In ‘Challenges and opportunities for enhancing sustainable cowpea production.’ Proceedings of the 3rd World Cowpea Conference, Ibadan, Nigeria 4–8 September 2000, IITA, Ibadan, Nigeria (Eds CA Fatokun, SA Tarawali, BB Singh, PM Kormawa, M Tamo) pp. 287–300. (IITA: Ibadan, Nigeria)

Singh BB, Ajeigbe HA, Tarawali SA, Fernandez-Rivera S, Abubakar M (2003) Improving the production and utilization of cowpea as food and fodder. Field Crops Research 84, 169–177.
Improving the production and utilization of cowpea as food and fodder.Crossref | GoogleScholarGoogle Scholar |

Slabbert R, Spreeth M, Kruger GHJ (2004) Drought tolerance, traditional crops and biotechnology: breeding towards sustainable development. South African Journal of Botany 70, 116–123.

Souza RP, Machado EC, Silva JAB, Lagoa AMMA, Silveira JAG (2004) Photosynhtetic gas exchange, chlorophyll fluorescence and some associated metabolic changes in cowpea (Vigna unguiculata) during water stress and recovery. Environmental and Experimental Botany 51, 45–56.
Photosynhtetic gas exchange, chlorophyll fluorescence and some associated metabolic changes in cowpea (Vigna unguiculata) during water stress and recovery.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXosVyh&md5=c39ca0a42c1245cc6ed442fc0cf30b98CAS |

Tanner CB, Sinclair TR (1983) Efficient water use in crop production: research or re-search? In ‘Limitations to efficient water use in crop production’. (Eds HM Taylor, WR Jordan, TR Sinclair) pp. 1–27. (American Society of Agronomy, Madison).

Tardieu F, Reymond M, Hamard P, Granier C, Muller B (2000) Spatial distributions of expansion rate, cell division rate and cell size in maize leaves: a synthesis of the effects of soil water status, evaporative demand and temperature. Journal of Experimental Botany 51, 1505–1514.
Spatial distributions of expansion rate, cell division rate and cell size in maize leaves: a synthesis of the effects of soil water status, evaporative demand and temperature.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXnt12juro%3D&md5=d0f5e83831f21a1df558a6172fe2611eCAS |

Vadez V, Sinclair TR (2001) Leaf ureide degradation and the N2 fixation tolerance to water deficit in soybean. Journal of Experimental Botany 52, 153–159.
Leaf ureide degradation and the N2 fixation tolerance to water deficit in soybean.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXhvVOit7g%3D&md5=99753175bdbce476bbd073b71bd2ce56CAS |

Vadez V, Krishnamurthy L, Serraj R, Gaur PM, Upadhyaya HD, Hoisington DA, Varshney RK, Turner NC, Siddique KHM (2007) Large variation in salinity tolerance in chickpea is explained by differences in sensitivity at the reproductive stage. Field Crops Research 104, 123–129.
Large variation in salinity tolerance in chickpea is explained by differences in sensitivity at the reproductive stage.Crossref | GoogleScholarGoogle Scholar |

Vadez V, Berger JD, Warkentin T, Asseng S, Ratnakumar P, Rao KPC, Gaur PM, Munier-Jolain N, Larmure A, Voisin AS, Sharma HC, Pande S, Sharma M, Krishnamurthy L, Zaman-Allah M (2012) Adaptation of grain legumes to climatic change: a review. Agronomy for Sustainable Development 32, 31–44.
Adaptation of grain legumes to climatic change: a review.Crossref | GoogleScholarGoogle Scholar |

van Duivenbooden N, Abdoussalam S, Mohamed AB (2002) Impact of climate change on agricultural production in the Sahel – part 2. Case study for groundnut and cowpea in Niger. Climatic Change 54, 349–368.
Impact of climate change on agricultural production in the Sahel – part 2. Case study for groundnut and cowpea in Niger.Crossref | GoogleScholarGoogle Scholar |

Wittig R, König K, Schmidt M, Szarzynski J (2007) A study of climate change and anthropogenic impacts in West Africa. Environmental Science and Pollution Research 14, 182–189.
A study of climate change and anthropogenic impacts in West Africa.Crossref | GoogleScholarGoogle Scholar |

Zaman-Allah M, Jenkinson DM, Vadez V (2011a) Chickpea genotypes contrasting for seed yield under terminal drought stress in the field differ for traits related to the control of water use. Functional Plant Biology 38, 270–281.
Chickpea genotypes contrasting for seed yield under terminal drought stress in the field differ for traits related to the control of water use.Crossref | GoogleScholarGoogle Scholar |

Zaman-Allah M, Jenkinson DM, Vadez V (2011b) A conservative pattern of water use, rather than deep or profuse rooting, is critical for the terminal drought tolerance of chickpea. Journal of Experimental Botany 62, 4239–4252.
A conservative pattern of water use, rather than deep or profuse rooting, is critical for the terminal drought tolerance of chickpea.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhtVeit7jJ&md5=6f53a4e57ec5de2e5ded9b6d3f768ae5CAS |