The multiple-stress effects on plant physiology and gene expression are being intensively studied lately, primarily in model plants such as Arabidopsis, where the effects of six stressors have simultaneously been documented. In maize, double and triple stress responses are obtaining more attention, such as simultaneous drought and heat or heavy metal exposure, or drought in combination with insect and fungal infestation. To keep up with these challenges, maize natural variation and genetic engineering are exploited. On one hand, quantitative trait loci (QTL) associated with multiple-stress tolerance are being identified by molecular breeding and genome-wide association studies (GWAS), which then could be utilized for future breeding programs of more resilient maize varieties. On the other hand, transgenic approaches in maize have already resulted in the creation of many commercial double or triple stress resistant varieties, predominantly weed-tolerant/insect-resistant and, additionally, also drought-resistant varieties. It is expected that first generation gene-editing techniques, as well as recently developed base and prime editing applications, in combination with the routine haploid induction in maize, will pave the way to pyramiding more stress tolerant alleles in elite lines/varieties on time.
Plant drought tolerance depends on adaptations of the photosynthetic apparatus to changing environments triggered by water deficit. The seedlings of three Brassica crops differing in drought sensitivity, Brassica oleracea L. var. capitata—white cabbage, Brassica oleracea L. var. acephala—kale, and Brassica rapa L. var. pekinensis—Chinese cabbage, were exposed to drought by withholding water. Detailed insight into the photosynthetic machinery was carried out when the seedling reached a relative water content of about 45% and after re-watering by analyzing the OJIP kinetics. The key objective of this study was to find reliable parameters for distinguishing drought−tolerant and drought-sensitive varieties before permanent structural and functional changes in the photosynthetic apparatus occur. According to our findings, an increase in the total performance index (PItotal) and structure–function index (SFI), positive L and K bands, total driving forces (ΔDF), and drought resistance index (DRI) suggest drought tolerance. At the same time, susceptible varieties can be distinguished based on negative L and K bands, PItotal, SFI, and the density of reaction centers (RC/CS0). Kale proved to be the most tolerant, Chinese cabbage was moderately susceptible, and white cabbage showed high sensitivity to the investigated drought stress. The genetic variation revealed among the selected Brassica crops could be used in breeding programs and high-precision crop management.
This study examined the photosynthetic responses of two sunflower hybrids to elevated temperatures and excess light intensity in the flowering stage by measuring the chlorophyll a fluorescence (ChlF) under morning and afternoon field conditions to determine the photosynthetic pigment contents and the relative accumulation of photosynthetic proteins. The morning environmental conditions were considered optimal, while the afternoon was characterised by elevated temperatures and excess light intensity. The minimum fluorescence intensity (F0), the electron-flux-reducing end electron acceptors at the photosystem I acceptor side per reaction centre (RE0/RC), and the D1 protein had significant, high, and positive correlations with the environmental conditions, which indicates that they were the most useful in the sunflower-stress-response research. In hybrid 7, the elevated temperatures and the excess light intensity resulted in the inactivation of the oxygen-evolving complex, which was indicated by the positive L, K, and J steps, the increase in the maximum quantum yield of PSII (TR0/ABS), the decrease in the electron transport further than the primary acceptor QA (ET0/(TR0-ET0)), the reduction in the performance index (PIABS), and the higher relative accumulation of the light-harvesting complex of the photosystem (LHCII). Hybrid 4 had smaller changes in the fluorescence curves in phases O–J and J–I, and especially in steps L, K, J, and I, and a higher PIABS, which indicates a more efficient excitation energy under the unfavourable conditions. As the tested parameters were sensitive enough to determine the significant differences between the sunflower hybrids in their photosynthetic responses to the elevated temperatures and excess light intensity in the flowering stage, they can be considered useful selection criteria. The development of more adaptable sunflower hybrids encourages sustainable sunflower production under stressful growing conditions.