Consistent Variation Across Soil Types in Salinity Resistance of a Diverse Range of Chickpea (Cicer arietinum L.) Genotypes

Chickpea is considered sensitive to salinity, but the salinity resistance of chickpea germplasm has rarely been explored. This study aimed to (i) determine whether there is consistent genetic variation for salinity resistance in the chickpea minicore and reference collections; (ii) determine whether the range of salinity resistance is similar across two of the key soil types on which chickpea is grown; (iii) assess the strength of the relationship between the yield under saline conditions and that under non‐saline conditions; and (iv) test whether salinity resistance is related to differences in seed set under saline conditions across soils and seasons. The seed yield of 265 chickpea genotypes in 2005–2006 and 294 cultivated genotypes of the reference set in 2007–2008 were measured. This included 211 accessions of the minicore collection of chickpea germplasm from the International Crops Research Institute for the Semi‐Arid Tropics (ICRISAT). The experiments were conducted in a partly controlled environment using a Vertisol soil in 2005–2006 and an Alfisol soil in 2007–2008, with or without 80 mm sodium chloride (NaCl) added prior to planting. In a separate experiment in 2006–2007, 108 genotypes (common across 2005–2006 and 2007–2008 evaluations) were grown under saline (80 mm NaCl) and non‐saline conditions in a Vertisol and an Alfisol soil. In 2005–2006 in the Vertisol and 2007–2008 in the Alfisol, salinity delayed flowering and maturity, and reduced both shoot biomass and seed yield at maturity. There was a large variation in seed yield among the genotypes in the saline pots, and a small genotype by environment interaction for grain yield in both soil types. The non‐saline control yields explained only 12–15 % of the variation of the saline yields indicating that evaluation for salinity resistance needs to be conducted under saline conditions. The reduction in yield in the saline soil compared with the non‐saline soil was more severe in the Alfisol than in the Vertisol, but rank order was similar in both soil types with a few exceptions. Yield reductions due to salinity were closely associated with fewer pods and seeds per pot (61–91 %) and to lesser extent from less plant biomass (12–27 %), but not seed size. Groups of consistently salinity resistant genotypes and the ones specifically resistant in Vertisols were identified for use as donor sources for crossing with existing chickpea cultivars.     

Legume genetic resources: management, diversity assessment, and utilization in crop improvement

Grain legumes contribute significantly to total world food production. Legumes are the primary source of dietary proteins in many developing countries, where protein hunger and malnutrition are widespread. Grain legumes germplasm constitute ~15% of the 7.4 M accessions preserved globally. Nearly, 78% of the CGIAR??s, 0.217 M accessions, have been characterized, compared to 34% of national genebank collections. Interestingly, limited data on grain quality are available as the primary focus has been on morpho-agronomic traits. Clearly, more resources should be targeted on biochemical evaluation to identify nutritionally rich and genetically diverse germplasm. The formation of core and mini core collections has provided crop breeders with a systematic yet manageable entry point into global germplasm resources. These subsets have been reported for most legumes and have proved useful in identifying new sources of variation. They may however not eliminate the need to evaluate entire collections, particularly for very rare traits. Molecular characterization and association mapping will further aid to insights into the structure of legume diversity and facilitate greater use of collections. The use of high resolution elevational climate models has greatly improved our capacity to characterize plant habitats and species?? adaptive responses to stresses. Evidence suggests that there has been increased use of wild relatives as well as new resources resulting from mutagenesis to enhance the genetic base of legume cultigens.     

Identification and inheritance of male sterility in groundnut (Arachis hypogaea L.)

Summary Some plants without pods but with gynophores were observed in two F₄ progenies of two crosses of goundnut (Arachis hypogaea L.). The flowers on these plants had translucent white anthers with no or a few sterile pollen grains. Three such plants in the succeeding generation were hand pollinated with pollen from a short-duration Indian cv. JL 24. The resulting F₁ hybrid plants (male sterile x JL 24) were normal. Chi-square tests for segregation for male fertile and male sterile plants in F₂ and F₃ generations indicated that the male sterility in these crosses of groundnut is governed by two recessive genes. We designate these genes as ms₁ and ms₂ with ms₁ms₁ms₂ms₂ being a male sterile genotype.Submitted as ICRISAT J. A. No. 1812.     

Geographical distribution of traits and diversity in the world collection of pearl millet [<Emphasis Type="Italic">Pennisetum glaucum</Emphasis> (L.) R. Br., synonym: <Emphasis Type="Italic">Cenchrus americanus</Emphasis> (L.) Morrone] landraces conserved at the ICRISAT genebank

The genebank at ICRISAT conserves the largest collection of 23,092 pearl millet germplasm accessions originating in 52 countries. A total of 15,979 landraces originating in 34 countries and having geographic coordinates of the collection sites were selected to investigate the geographical distribution of pearl millet traits and diversity in the collection. Results revealed adaptation of pearl millet to latitudes ranging between 33.00°S and 36.91°N. Landraces with early flowering (33–40 days) were predominant in Pakistan, Ghana, Togo and India; with very late flowering (121–159 days) in Sierra Leone and the Central African Republic; with short plant height (80–100 cm) in India, Zambia and Sudan; with tallness (401–490 cm) in Chad, Burkina Faso, Nigeria and the Central African Republic; with high tillering (11–35) in India and Yemen; with high panicle exsertion (11–29 cm) in Ghana, Chad, India and Yemen; with long panicles (75–135 cm) in Nigeria and Niger; with thick panicles (41–58 mm) in Namibia, Togo and Zimbabwe and those with large seeds (16–19 g 1000 seeds^?1) were predominant in Togo, Benin, Ghana and Burkina Faso. Collections from Ghana for flowering (36–150 days), Burkina Faso for plant height (80–490), India and Yemen for total (1–35) and productive (1–19) tillers per plant, Niger for panicle exsertion (?45 to 21.0), panicle length (9–135 cm) and thickness (12–55 mm) and Zimbabwe for 1000 seed weight (3.5–19.3 g), were found as important sources for trait diversity. Launching collection missions for trait-specific germplasm is suggested to enrich the world collection of pearl millet at ICRISAT genebank for diversity.     

Inheritance of two components of early maturity in groundnut (Arachis hypogaea L.)

Summary Knowledge of inheritance of early maturity or its components is important to groundnut breeders in developing short-duration cultivars. This study was conducted to determine the inheritance of two components of early maturity: days to first flower from sowing, and days to accumulation of 25 flowers from the appearance of first flower, using three groundnut genotypes. Two early-maturing (Chico and Gangapuri) and one late-maturing (M 13) genotypes were crossed in all possible combinations, including reciprocals. The parents, F₁, F₂, F₃, and backcross populations were evaluated for days to first flower from sowing, and for days to accumulation of 25 flowers. The data suggest that days to first flower in the crosses studied is governed by a single gene with additive gene action. Chico and Gangapuri possess the same allele for this component of earliness. Three independent genes with complete dominance at each locus appear to control the days to accumulation of 25 flowers. In crosses between late (M 13) and early (Chico or Gangapuri) parents, a segregation pattern suggesting dominant-recessive epistasis (13 late:3 early) was observed for this component. Segregation in the F₂ generation (1 late:15 early) of both early parents (Chico x Gangapuri) indicated that the genes for early accumulation of flowers in these two parents are at different loci.Submitted as ICRISAT J.A. No. 1557.     

Patterns of diversity in pigeonpea (<Emphasis Type="Italic">Cajanus cajan</Emphasis> (L.) Millsp.) germplasm collected from different elevations in Kenya

Pigeonpea germplasm accessions collected from low (<500 m), medium (501–1000 m), high (1001–1500 m) and very high elevation zones (>1500 m) of Kenya were evaluated for 15 agronomic traits and seed protein content at ICRISAT, Patancheru, India. There were significant differences (P < 0.001) among elevation zones for the number of primary and secondary branches, days to 75% maturity, pod length, seeds per pod, 100-seed weight and seed yield. Mean values indicated that the accessions from low elevation zone were significantly different from those collected in higher elevation zones for early flowering and maturity, number of primary branches, pod length, number of pods per plant, seeds per pod, 100-seed weight, seed yield and harvest index. None of the accessions collected in Kenya belonged to extra early (<80 days to 50% flowering) and early (80–100 days to 50% flowering) maturity groups, as defined by time to flowering at Patancheru, India. Mean diversity index based on all characters indicated that accessions from the low elevation zone are more diverse than those from the higher elevation zones. Frequency distribution for trait extremes indicated that the accessions from the low elevation zone were early to flower and mature, short statured, produced more primary and secondary branches with high pod bearing length, long pods, more pods per plant, more seeds per pod, a high seed yield and harvest index. Accessions from the very high elevation zone were late flowering, with a large number of tertiary branches, large seeds and a high shelling percentage and could be a source for cold tolerance and the breeding of vegetable types. Results suggest that the elevation of collection sites is therefore a very important determinant of variation patterns of pigeonpea in Kenya.     

Identification of diverse genotypes with high oil content in Madhuca latifolia for further use in tree improvement

Madhuca latifolia Macb.commonly known as Indian butter tree,is an open-pollinated plant.Improvement in seed and oil yields depends on the progress in the desired characters in the base material and the genetic variability available in the collected germplasm.We evaluated 23 genotypes of M.latifolia to understand genetic variability,character association and divergence in seed traits and oil content for use in breeding programs.Variation was recorded in seed length(27.3–38.6 mm),seed breadth(15.6–19.1 mm),two dimensional(2D) surface area(328.3–495.4 mm2),100 seed weight(216.8–285.3 g),acid value(13.4–25.8 mg KOH/g),iodine number(62.4–78.6) and oil content(37.8–51.0 %).High estimates of genotypic coefficient of variation,broad senseheritability and genetic gain were observed for seed oil content.Variability studies for seed traits revealed that genotype CPT-16 had the highest 100-seed weight(281.5 g) and oil content(51 %).Highly significant genotypic and phenotypic correlations were observed.The100-seed weight was positively and significantly correlated with oil content at both phenotypic(r = 0.57) and genotypic(r = 0.60) levels.Cluster analysis of the scores of the first three principle components(80.83 %) resulted in four clusters,consisting of 4,7,3 and 9 genotypes in the first,second,third and fourth clusters,respectively.Cluster 3was distinguished from others based on significantly higher means for most seed traits except seed breadth,acid value,iodine number and oil content.Cluster 1 appeared more divergent as it had significantly higher means for acid value and iodine number.A comparative assessment of means of the four clusters for 100-seed weight and oil content suggested that cluster 3 would be useful for higher 100-seed weight and oil content.Hence these genotypes,CPT-3,CPT-6 and CPT-15 in cluster 3 can be used for direct selection and utilization in breeding programs.