Morpho-Physiological Mechanisms of Maize for Drought Tolerance

Maize is one of the mostly consumed grains in the world. It possesses a greater potentiality of being an alternative to rice and wheat in the near future. In field condition, maize encounters abiotic stresses like salinity, drought, water logging, cold, heat, etc. Physiology and production of maize are largely affected by drought. Drought has become a prime cause of agricultural disaster because of the major occurrence records of the last few decades. It leads to immense losses in plant growth (plant height and stem), water relations (relative water content), gas exchange (photosynthesis, stomatal conductance, and transpiration rate), and nutrient levels in maize. To mitigate the effect of stress, plant retreats by using multiple morphological, molecular, and physiological mechanisms. Maize alters its physiological processes like photosynthesis, oxidoreductase activities, carbohydrate metabolism, nutrient metabolism, and other drought-responsive pathways in response to drought. Synthesis of some chemicals like proline, abscisic acid (ABA), different phenolic compounds, etc. helps to fight against stress. Inoculation of plant growth-promoting rhizobacteria (PGPR) can result to the gene expression involved in the biosynthesis of abscisic acid which also helps to resist drought. Moreover, adaptation to drought and heat stress is positively influenced by the activity of chaperone proteins and proteases, protein that responds to ethylene and ripening. Some modifications generated by clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9 are able to improve maize yield in drought. Forward and reverse genetics and functional and comparative genomics are being implemented now to overcome stress conditions like drought. Maize response to drought is a multifarious physiological and biochemical process. Applying data synthesis approach, this study aims toward better demonstration of its consequences to provide critical information on maize tolerance along with minimizing yield loss.

Heat and Drought Stresses in Wheat (Triticum aestivum L.): Substantial Yield Losses, Practical Achievements, Improvement Approaches, and Adaptive Mechanisms

The major wheat-producing countries have heterogeneous and fragile agro climatic surroundings but frequently restraining wheat yield and quality losses are predominant under heat and drought prone agriculture exclusively when both stresses occur in blend, which looms the food security globally. However, many suggested examples are available in these countries for the mitigation of these two stresses by using different conventional and modern improvement and agronomic approaches. In addition to these approaches, morphological, physiological, anatomical, biochemical, phenological, and physiochemical vicissitudes, which trigged during these stresses, have also been elucidated. There complete deliberation in combination for wheat improvement is still a contest, but a win-win option is a holistic attitude in future.

The Impact of Changing Climate on the Cambial Activity during Radial Growth in Some Citrus Species

This study on radial growth in the stem of Citrus was carried out with an aim to notice the behavior of vascular cambium with respect to climatic and age effects. The fusiform initials vary in length from 137 to 363 μm in C. limon, 100 to 463 μm in C. paradisi, 137 to 413 μm in C. reticulata var. kinnow, and 137 to 375 μm in C. sinensis. The length rises with age, followed by decline and then again increase in C. limon. In C. paradisi, there is increase up to maximum and after decline is soon followed by constancy. In C. reticulata var. kinnow, increase in length from top to base in C. sinensis, increase up to maximum followed by a decline. Swelling of cambial cells occurs in the third week of March in C. limon, last week of March in C. paradisi, third week of April in C. reticulata var. kinnow, and second week of April in C. sinensis. The cambium turns dormant in early October in C. limon, late December in C. paradisi, early December in C. reticulata var. kinnow, and early November in C. sinensis. Thus, the cambium remains active for about 6 months in C. limon and C. sinensis, 9 months in C. paradisi, and 7 months in C. reticulata var. kinnow.