Selection of Soybean and Cowpea Cultivars with Superior Performance under Drought Using Growth and Biochemical Aspects

Identifying cultivars of leguminous crops exhibiting drought resistance has become crucial in addressing water scarcity issues. This investigative study aimed to select soybean and cowpea cultivars with enhanced potential to grow under water restriction during the vegetative stage. Two parallel trials were conducted using seven soybean (AS3810IPRO, M8644IPRO, TMG1180RR, NS 8338IPRO, BMX81I81IPRO, M8808IPRO, and BÔNUS8579IPRO) and cowpea cultivars (Aracê, Novaera, Pajeú, Pitiúba, Tumucumaque, TVU, and Xique-xique) under four water levels (75, 60, 45, and 30% field capacity—FC) over 21 days. Growth, water content, membrane damage, photosynthetic pigments, organic compounds, and proline levels were analyzed. Drought stress significantly impacted the growth of both crops, particularly at 45 and 30% FC for soybean and 60 and 45% FC for cowpea plants. The BÔNUS8579IPRO and TMG1180RR soybean cultivars demonstrated the highest performance under drought, a response attributed to increased amino acids and proline contents, which likely help to mitigate membrane damage. For cowpea, the superior performance of the drought-stressed Xique-xique cultivar was associated with the maintenance of water content and elevated photosynthetic pigments, which contributed to the preservation of the photosynthetic efficiency and carbohydrate levels. Our findings clearly indicate promising leguminous cultivars that grow under water restriction, serving as viable alternatives for cultivating in water-limited environments.

[1]  K. Siddique,et al.  Plant photosynthetic responses under drought stress: Effects and management , 2023, Journal of Agronomy and Crop Science.

[2]  Hai Nguyen,et al.  Impacts of Historical Droughts on Maize and Soybean Production in the Southeastern United States , 2023, SSRN Electronic Journal.

[3]  The United Nations World Water Development Report 2023 , 2023, The United Nations World Water Development Report.

[4]  P. Bebeli,et al.  Cowpea Constraints and Breeding in Europe , 2023, Plants.

[5]  V. Pande,et al.  Coordinated regulation of photosynthesis and sugar metabolism in guar increases tolerance to drought , 2022, Environmental and Experimental Botany.

[6]  O. Babalola,et al.  Constraints and Prospects of Improving Cowpea Productivity to Ensure Food, Nutritional Security and Environmental Sustainability , 2021, Frontiers in Plant Science.

[7]  R. O. Mesquita,et al.  Salt-Acclimation Physiological Mechanisms at the Vegetative Stage of Cowpea Genotypes in Soils from a Semiarid Region , 2021, Journal of Soil Science and Plant Nutrition.

[8]  F. Marin,et al.  Impact assessment of soybean yield and water productivity in Brazil due to climate change , 2021 .

[9]  S. Chaudhry,et al.  Climate change regulated abiotic stress mechanisms in plants: a comprehensive review , 2021, Plant Cell Reports.

[10]  Mengxue Liu,et al.  Effect of drought on photosynthesis, total antioxidant capacity, bioactive component accumulation, and the transcriptome of Atractylodes lancea , 2021, BMC Plant Biology.

[11]  M. A. Khan,et al.  Drought: Sensing, Signalling, Effects and Tolerance in Higher Plants. , 2021, Physiologia plantarum.

[12]  J. A. Teixeira da Silva,et al.  Water stress modifies canopy light environment and qualitative and quantitative yield components in two soybean varieties , 2021, Irrigation Science.

[13]  M. Ozturk,et al.  Osmoregulation and its actions during the drought stress in plants. , 2020, Physiologia plantarum.

[14]  Tomislav Tosti,et al.  Leaf Soluble Sugars and Free Amino Acids as Important Components of Abscisic Acid—Mediated Drought Response in Tomato , 2020, Plants.

[15]  L. M. Sandalio,et al.  Effect of drought on growth, photosynthesis and total antioxidant capacity of the saharan plant Oudeneya africana , 2020, Environmental and Experimental Botany.

[16]  Shengyou Li,et al.  Screening diverse soybean genotypes for drought tolerance by membership function value based on multiple traits and drought-tolerant coefficient of yield , 2020, BMC Plant Biology.

[17]  R. E. Mason,et al.  Evaluation of Drought Tolerance in Arkansas Cowpea Lines at Seedling Stage , 2020, HortScience.

[18]  K. R. Reddy,et al.  Proteomics, physiological, and biochemical analysis of cross tolerance mechanisms in response to heat and water stresses in soybean , 2020, PloS one.

[19]  Fang Wang,et al.  Impacts of Drought on Maize and Soybean Production in Northeast China During the Past Five Decades , 2020, International journal of environmental research and public health.

[20]  M. Loureiro,et al.  Physiological approach to decipher the drought tolerance of a soybean genotype from Brazilian savana. , 2020, Plant physiology and biochemistry : PPB.

[21]  S. Fahad,et al.  Seed priming with melatonin coping drought stress in rapeseed by regulating reactive oxygen species detoxification: Antioxidant defense system, osmotic adjustment, stomatal traits and chloroplast ultrastructure perseveration , 2019, Industrial Crops and Products.

[22]  J. Ahmad,et al.  Drought mediated physiological and molecular changes in muskmelon (Cucumis melo L.) , 2019, PloS one.

[23]  Bohdan Dukhnytskyi World agricultural production , 2019, Ekonomika APK.

[24]  M. Egea-Cortines,et al.  Evaluating stress responses in cowpea under drought stress. , 2019, Journal of plant physiology.

[25]  A. Sher,et al.  Research Progress and Perspective on Drought Stress in Legumes: A Review , 2019, International journal of molecular sciences.

[26]  J. H. Costa,et al.  Salt acclimation in sorghum plants by exogenous proline: physiological and biochemical changes and regulation of proline metabolism , 2019, Plant Cell Reports.

[27]  R. O. Mesquita,et al.  Nitrogen assimilation pathways and ionic homeostasis are crucial for photosynthetic apparatus efficiency in salt-tolerant sunflower genotypes , 2018, Plant Growth Regulation.

[28]  R. O. Mesquita,et al.  Nitrogen assimilation pathways and ionic homeostasis are crucial for photosynthetic apparatus efficiency in salt-tolerant sunflower genotypes , 2018, Plant Growth Regulation.

[29]  S. Vats,et al.  Biotic and Abiotic Stress Tolerance in Plants , 2018, Springer Singapore.

[30]  V. S. Bhatia,et al.  Impact of combined stress of high temperature and water deficit on growth and seed yield of soybean , 2018, Physiology and Molecular Biology of Plants.

[31]  V. S. Bhatia,et al.  Impact of combined stress of high temperature and water deficit on growth and seed yield of soybean , 2017, Physiology and Molecular Biology of Plants.

[32]  N. Hassan,et al.  Exogenous applications of Polyamines modulate drought responses in wheat through osmolytes accumulation, increasing free polyamine levels and regulation of polyamine biosynthetic genes. , 2017, Plant physiology and biochemistry : PPB.

[33]  A. S. Melo,et al.  Antioxidative Responses of Cowpea Cultivars to Water Deficit and Salicylic Acid Treatment , 2017 .

[34]  H. Trindade,et al.  Cowpea (Vigna unguiculata L. Walp.) Metabolomics: Osmoprotection as a Physiological Strategy for Drought Stress Resistance and Improved Yield , 2017, Front. Plant Sci..

[35]  E. Braga,et al.  Correlation of proline content and gene expression involved in the metabolism of this amino acid under abiotic stress , 2016, Acta Physiologiae Plantarum.

[36]  Ó. Vicente,et al.  Breeding and Domesticating Crops Adapted to Drought and Salinity: A New Paradigm for Increasing Food Production , 2015, Front. Plant Sci..

[37]  K. Abdelaal EFFECT OF SALICYLIC ACID AND ABSCISIC ACID ON MORPHO-PHYSIOLOGICAL AND ANATOMICAL CHARACTERS OF FABA BEAN PLANTS (Vicia faba L.) UNDER DROUGHT STRESS , 2015 .

[38]  F. Damatta,et al.  Salt stress tolerance in cowpea is poorly related to the ability to cope with oxidative stress , 2014 .

[39]  Daniel Furtado Ferreira,et al.  Sisvar: a computer statistical analysis system , 2011 .

[40]  J. Flexas,et al.  Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. , 2009, Annals of botany.

[41]  A. Wellburn The Spectral Determination of Chlorophylls a and b, as well as Total Carotenoids, Using Various Solvents with Spectrophotometers of Different Resolution* , 1994 .

[42]  I. D. Teare,et al.  Rapid determination of free proline for water-stress studies , 1973, Plant and Soil.

[43]  C. Fraisse,et al.  Yield gap in cowpea plants as function of water déficits during reproductive stage , 2020 .

[44]  Jitender Singh,et al.  Photosynthesis and Abiotic Stress in Plants , 2018 .

[45]  R. O. Mesquita,et al.  Nitrate: ammonium nutrition alleviates detrimental effects of salinity by enhancing photosystem II efficiency in sorghum plants , 2014 .

[46]  R Core Team,et al.  R: A language and environment for statistical computing. , 2014 .

[47]  F. Smith,et al.  Colorimetric Method for Determination of Sugars and Related Substances , 1956 .

[48]  E. W. Yemm,et al.  The determination of amino-acids with ninhydrin , 1955 .