No abstract

Chickpea is sensitive to low temperature (<10°C) during its reproductive stage. Low temperature adversely affects the development of pods and seeds. This study was undertaken to investigate the role of sucrose metabolizing enzymes in seed development and potential of antioxidative enzymes in protecting seeds and podwalls from the deleterious effects of cold stress in advanced cold tolerant chickpea breeding lines. Healthy pod set was observed in these tolerant lines in the end of December where as low temperature susceptible PBG‐1 did not flower. Two lines ICCV 96029 and ICCV 96030 showed susceptible characters such as reduced flowering, blackened and shrivelled seeds and yellowish pods in comparison to other cold stress tolerant lines due to sudden dip of temperature (<1 °C) during the first week of January. These two lines were, therefore, treated as susceptible checks in comparison to other tolerant lines. A significantly higher activity and specific activity of sucrose synthase was observed in seeds of most of the cold tolerant lines in comparison with ICCV 96029 and ICCV 96030, thereby providing sugars as well as sugar nucleotides for their growth and starch synthesis during unfavourable low temperature. The developing seeds and podwalls of tolerant genotypes had higher activities of antioxidant enzymes, i.e. catalase, ascorbate peroxidase and glutahione reductase in comparison with ICCV 96029 and ICCV 96030. It appears that the higher activities of antioxidant enzymes in podwall protect the developing seeds from cold stress.

Recently, a breeding technology for hybrid pigeonpea [Cajanus cajan (L.) Millsp.] based on cytoplasmic‐nuclear male sterility (CMS) and partial natural outcrossing was developed at ICRISAT. The limited number of experimental hybrids tested has shown the presence of a considerable amount of hybrid vigor for seed yield. In the present study, one extra‐early‐ (120 d), two early‐ (150 d), and two late‐maturing (180 d) pigeonpea hybrids were studied to generate information on the genetics of fertility restoration of the A4 CMS system. In the extra‐early‐maturing hybrids, pollen fertility was controlled by a single dominant gene, whereas in the early‐ and late‐ maturing hybrids, male fertility was governed by two duplicate dominant genes. It was also observed that hybrids with two dominant genes produced a greater pollen load and expressed greater stability as compared with those carrying a single dominant gene. The information on the inheritance of fertility restoration will help in designing strategies for breeding elite hybrid parents, and it was concluded that for breeding hybrids with stable fertility restoration, the presence of two dominant genes is essential.

Fusarium wilt (FW; caused by Fusarium oxysporum f. sp. ciceris) and Ascochyta blight (AB; caused by Ascochyta rabiei) are two major biotic stresses that cause significant yield losses in chickpea (Cicer arietinum L.). In order to identify the genomic regions responsible for resistance to FW and AB, 188 recombinant inbred lines derived from a cross JG 62 9 ICCV 05530 were phenotyped for reaction to FW and AB under both controlled environment and field conditions. Significant variation in response to FW and AB was detected at all the locations. A genetic map comprising of 111 markers including 84 simple sequence repeats and 27 single nucleotide polymorphism (SNP) loci spanning 261.60 cM was constructed. Five quantitative trait loci (QTLs) were detected for resistance to FW with phenotypic variance explained from 6.63 to 31.55%. Of the five QTLs, three QTLs including a major QTL on CaLG02 and a minor QTL each on CaLG04 and CaLG06 were identified for resistance to race 1 of FW. For race 3, a major QTL each on CaLG02 and CaLG04 were identified. In the case of AB, one QTL for seedling resistance (SR) against 'Hisar race' and a minor QTL each for SR and adult plant resistance against isolate 8 of race 6 (3968) were identified. The QTLs and linked markers identified in this study can be utilized for enhancing the FW and AB resistance in elite cultivars using marker-assisted backcrossing.

Whitefly, Bemisia tabaci (Gennadius) (Hemiptera: Aleryrodidae), is a serious pest of black gram, (Vigna mungo (L.) Hepper), an important legume pulse crop grown in north India. This research investigated the potential role of selected plant oxidative enzymes in resistance/susceptibility to whitefly in nine black gram genotypes. Oxidative enzyme activity was estimated spectrophotometrically from leaf samples collected at 30 and 50 d after sowing (DAS) from whitefly infested and uninfested plants. The enzymes showed different activity levels at different times after the infestation. The results indicated that in general, whitefly infestation increased the activities of peroxidase and decreased the catalase activity. Resistant genotypes NDU 5-7 and KU 99-20 recorded higher peroxidase and catalase activities at 30 and 50 DAS under whitefly-stress conditions as compared with non-stressed plants. The results suggest that the enhanced activities of the enzymes may contribute to bioprotection of black gram plants against B. tabaci infestation. The potential mechanisms to explain the correlation of resistance to whitefly in black gram genotypes with higher activities of oxidative enzymes are also discussed.