Generation and characterisation of colchicine-induced polyploid Lavandula × intermedia

Double podding in cultivated chickpeas (Cicer arietinum L.) can increase yield and yield stability. In the present study, we performed reciprocal crosses of ‘kabuli’ (double podded) and ‘desi’ (single podded) chickpeas to determine (i) the expressivity and penetrance of double podding, (ii) the correlations of yield and yield components, and (iii) the heritability of double podding, flower color, and stem pigmentation in F₂ plants. Reciprocal crosses were performed with two genotypes, AC 2969 (kabuli) and ICC 4969 (desi), to generate F₁ and F₂ plants. The results indicated hybrid vigor (heterosis) for yield in F₁ plants and better performance of F₂ plants. Yield and yield components of some lines in F₂ were superior to the best parent, indicative of transgressive segregation. In particular, the presence of double podding (‘s’ allele) significantly increased yield in some of the transgressive segregants. Expressivity and penetrance of the ‘s’ allele depends on the background of the female parent. Some of the double podding progeny had greater seed yields than those of the single podding progeny and greater seed yields than the best parents. Double podding, stem pigmentation, and pink flowers each appears to be governed by a single recessive gene. Stem pigmentation and pink flowers appear to be linked traits that depend on the genetic background of the crossed chickpeas. Taken together, our studies of reciprocal crosses of kabuli and desi chickpeas clearly showed that yield could be improved by selection for transgressive phenotypes that have double podding.     

Mapping genes for double podding and other morphological traits in chickpea

Seed traits are important considerations for improving yield and product quality of chickpea (Cicer arietinum L.). The purpose of this study was to construct an intraspecific genetic linkage map and determine map positions of genes that confer double podding and seed traits using a population of 76 F₁₀ derived recombinant inbred lines (RILs) from the cross of ‘ICCV-2’ (large seeds and single pods) × ‘JG-62’ (small seeds and double podded). We used 55 sequence-tagged microsatellite sites (STMS), 20 random amplified polymorphic DNAs (RAPDs), 3inter-simple sequence repeats (ISSR) and 2 phenotypic markers to develop a genetic map that comprised 14 linkage groups covering297.5 cM. The gene for double podding (s) was mapped to linkage group 6 and linked to Tr44 and Tr35 at a distance of7.8 cM and 11.5 cM, respectively. The major gene for pigmentation, C, was mapped to linkage group 8 and was loosely linked to Tr33 at a distance of 13.5 cM. Four QTLs for 100 seed weight (located on LG4 and LG9), seed number plant^-1 (LG4), days to 50% flower (LG3) were identified. This intraspecific map of cultivated chickpea is the first that includes genes for important morphological traits. Synteny relationships among STMS markers appeared to be conserved on six linkage groups when our map was compared to the interspecific map presented by Winter et al. (2000). This revised version was published online in August 2006 with corrections to the Cover Date.     

Transgressive segregations for yield criteria in reciprocal interspecific crosses between <Emphasis Type="Italic">Cicer arietinum</Emphasis> L. and <Emphasis Type="Italic">C. reticulatum</Emphasis> Ladiz.

Wild Cicer species are considered to be more resistant for biotic and abiotic stresses than that of the cultivated chickpea (Cicer arietinum L.). Alien genes conferring resistance for biotic and abiotic stresses can be transferred from wild Cicer species to the cultivated chickpea but success in interspecific hybridizations has already been achieved with only two wild Cicer species. The current study was undertaken to compare fruitful heterosis in F₂ and F₃ for yield and yield criteria and to identify transgressive segregation in F₂ and F₃ in reciprocal interspecific crosses between C. arietinum and C. reticulatum Ladiz. We define fruitful heterosis as a useful parameter that can be used instead of residual heterosis. Considerable fruitful heterosis in F₂ and F₃ was found for number of seeds, pods per plant, biological yield, and seed yield. Maximum values of most of the characteristics in F₂ and F₃ were higher than that of the best parent indicating that superior progeny could be selected for yield from transgressive segregation. Progeny selection should be based on number of seeds, pods per plant, and biological yield since these characteristics had the highest direct effect on seed yield. The narrow sense heritability was found to be the highest for 100-seed weight. It was suggested that the cultivated chickpea could be used as female parent in interspecific hybridization to increase yield and yield criteria since progeny in F₂ and F₃ had better performance when it was used as female. In conclusion, interspecific hybridization of wild and cultivated chickpea can be used to improve yield and yield components and resistance to biotic and abiotic stresses as well.     

Independent selection for seed free tryptophan content and vernalization response in chickpea domestication

Chickpea shows a distinct domestication trajectory vis‐a‐vis pod dehiscence and growth cycle mediated by vernalization insensitivity compared with its companion Near Eastern legumes. Our objectives were: (i) to map the quantitative trait loci (QTLs) associated with vernalization response and seed free tryptophan in domesticated × wild chickpea progeny and (ii) estimate the genetic correlation between vernalization response and free tryptophan content. A domesticated × wild chickpea cross was used to document phenotypic segregation in both traits and to construct a skeletal genetic map for QTL detection. A number of vernalization response and seed free tryptophan content QTLs were documented in both F₂ and F₃ generations. No significant genetic correlation between these two traits was observed. Epistatic relationship between two free tryptophan loci was documented. It is evident that selection for high seed tryptophan is easier to accomplish relative to selection for vernalization insensitivity. This suggests that the two traits were selected independently in antiquity, thereby corroborating earlier claims for conscious selection processes associated with chickpea domestication.     

Broadening the genetic base of lentil cultivars through inter‐sub‐specific and interspecific crosses of Lens taxa

Wild Lens taxa are invaluable sources of useful traits for broadening genetic base of cultivated lentil. Nine inter‐sub‐specific and interspecific crosses were made successfully between cultivated (Lens culinaris ssp. culinaris) and wild lentils (L. culinaris ssp. orientalis, odemensis, lamottei and ervoides). The effect of species groups, day length and temperature on crossability in lentils was evident under normal winter sowing in New Delhi and in summer Himalayan nursery at Sangla in Himachal Pradesh, India, although pollen fertility assessed in all the cross‐combinations showed no significant variation. True hybridity of nine inter‐sub‐specific and interspecific crosses was confirmed through morphological and molecular (ISSR) markers, in which three of 120 primers could confirm the hybridity of all the crosses. All cross‐combinations were also studied for important quantitative traits related to yield. The range, mean and coefficient of variation were estimated in parental lines, F₁ and F₂ generations to determine the extent of variability generated in cultivated lentils through the introgression of genes from wild L. taxa. A high level of heterosis was observed in F₁ crosses for important traits studied. Substantially higher variations for seed yield and its attributing traits were exhibited in F₂ generations indicating transgressive segregation. The results of the present investigation revealed that wild L. taxa can be successfully exploited for lentil improvement programmes, and the variations generated could be easily utilized for broadening the genetic base of cultivated lentil gene pool for improving the yield as well as wider adaptation.     

Pollen grain germination and pollen tube growth following in vivo and in vitro self and interspecific pollinations in annual Cicer species

Summary Germination of pollen grains and growth of pollen tubes were studied to determine the cause of barreness in crosses among annual Cicer species. In vivo and in vitro time-course studies and fluorescent microscopy revealed no pollination incompatibility among the selfs, crosses and reciprocals of C. arietinum L., C. reticulatum Lad. and C. cuneatum Rich. In general, Cicer pollen grains germinated and grew on styles of Cicer species. Pollen tube growth was characterized by irregularly spaced and intermittent callose deposits. Failure of seed formation in interspecific pollinations may be attributed to the slowness of pollen tube growth or collapse of fertilized ovules. In addition to these causes, shortness of stamens and sparsity of pollen grains were responsible for flower drop in natural selfs. Although the number of pollen tubes entering the micropyle in interspecific pollinations was low, it may be possible to grow the fertilized ovules on an artificial medium to obtain F₁ plants.     

Introgression from wild Cicer reticulatum to cultivated chickpea for productivity and disease resistance

Interspecific hybridization is known to improve productivity and resistance to diseases in many crops. Therefore, an attempt was made to introgress productivity and disease resistance into chickpea from wild Cicer species. The true F₁ hybrids of cultivated chickpea genotypes ‘L550’ and ‘FGK45’ with C. reticulatum were backcrossed twice to their cultivated female parents to minimize the linkage drag of undesirable wild traits. The pedigree method was followed to advance the segregating populations from straight crosses (without backcross) and BC₁/BC₂ generations to F₅–F₇. The interspecific derivatives recorded up to a 16.9% increase over the check cultivars and a 25.2% increase over the female parent in a preliminary yield evaluation trial. Of the 22 interspecific derivatives thus derived, four desi and two kabuli lines were further evaluated for seed yield in replicated trials at three diverse locations. These lines possess a high degree of resistance to wilt, foot rot and root rot diseases, and recorded a 6.1–17.0% seed yield increase over the best check cultivars.     

Exploitation of wild annual Cicer species for widening the gene pool of chickpea cultivars

Introgression of unadapted genes from the wild Cicer species could contribute to the widening of genetic base of important traits such as yield, yield attributes and resistance to major biotic and abiotic stresses. An attempt was made successfully to intercross two wild annual Cicer species with three cultivated chickpea cultivars. Four interspecific cross‐combinations were made, and their true hybridity was ascertained through morphological and molecular markers. These cross‐combinations were also studied for some important quantitative traits under real field conditions. The range, mean and coefficient of variation of agro‐morphological traits were assessed in the parental lines, their F₁ and F₂ generations to determine the extent of variability generated in cultivated chickpea varieties. A high level of heterosis was recorded for number of pods/plant and seed yield/plant in F₁ generation. Three cross‐combinations of ‘Pusa 1103’ × ILWC 46, ‘Pusa 256’ × ILWC 46 and ‘Pusa 256’ × ILWC 239 exhibited substantially higher variability for important yield‐related traits. The present research findings indicate that these wild annual Cicer species can be easily exploited to broaden the genetic base of cultivated gene pool for improving seed yield as well as adaptation.     

Ovule and embryo culture to obtain hybrids from interspecific incompatible pollinations in chickpea

Many of the wild species of chickpea were not accessible to the improvement of chickpea due to cross incompatibility. In these interspecific incompatible crosses, fertilization takes place but the embryo aborts a few days later. The only way to obtain hybrid plants is by the application of growth regulators to pollinated pistils to prevent initial pod abscission and to save the aborting hybrid embryos by embryo rescue techniques. Although there are a few papers on regeneration from different explants of chickpea, information on embryo rescue techniques is not available. The paper summarises the embryo rescue techniques developed for chickpea, by the use of which hybrid plants between C. arietinum and C. pinnatifidum were produced. The paper also emphasises the effect of genotype to successfully obtain hybrids. The morphology of the hybrid plants resembled the male parent in leaf structure and growth habit. The colour of the flowers produced on the hybrid plant was pale violet, resembling the male parent whose flowers were violet in colour. The flower colour of the female parent was white. This revised version was published online in August 2006 with corrections to the Cover Date.     

Investigations into the Barrier(s) to Interspecific Hybridization between Cicer arietinum L. and eight other Annual Cicer species

Barrier(s) to interspecific hybridization between the cultivated chickpea, Cicer arietinum L., and eight other annual wild species, i.e. C. reticulatum Lad., C. echinospermum Dav., C. pinnatifidum J. and S., C. judaicum Boiss., C. bijugum Rech., C. chorassanicum (Bge) M. Pop., C. yamashitae Kit. and C. cuneatum Rich., were investigated. In general, good pollen germination and pollen tube growth were observed in all eight crosses and their reciprocals. En spite of a few pollen cube growth abnormalities in most crosses, pollen tube penetration into the ovule and, thus, fertilization was observed in all cross combinations. However, differences were observed in the time from pollination to fertilization, not only between different interspecific crosses but also between reciprocals of a particular interspecific cross. The crossability barrier is, therefore, believed to be due to factor(s) operating after fertilization.     

A gene producing one to nine flowers per flowering node in chickpea

Chickpea (Cicer arietinum L.) has a racemose type of inflorescence and at each axis of the raceme usually one or two and rarely three flowers are borne. Plants producing 3 to 9 flowers, arranged in acymose inflorescence, at many axis of the raceme, were identified in F₂ of an interspecific cross ICC 5783 (C. arietinum) × ICCW 9 (C. reticulatum)in which both the parents involved were single-flowered. A spontaneous mutation in one of the two parents or in the F₁was suspected. However, the possibility for establishment of a rare recombination of two interacting recessive genes could not be ruled out. The number of pods set varied from 0 to 5 in each cyme. Inheritance studies indicated that a single recessive gene, designated cym, is responsible for cymose inflorescence. The allelic relationship of cym with sfl, a gene for double-flowered trait, was studied from a cross involving multi flowered plants and the double-flowered line ICC 4929. Thecym gene was not allelic to sfl, suggesting that two loci control the number of flowers per peduncle in chickpea. The cym locus segregated independently of the locus sfl, ifc (inhibitor of flower color) and blv (bronze leave). This revised version was published online in August 2006 with corrections to the Cover Date.     

The origin of chickpea Cicer arietinum L.

Summary Species relationship between the cultivated chickpea Cicer arietinum and the two newly discovered wild species C. echinospermum and C. reticulatum were assessed through breeding experiments and cytological examination of the hybrids.The two wild species differed from each other by a major reciprocal translocation and their hybrid was completely sterile. The wild species C. echinospermum also differed from the cultivated species by the same translocation and their hybrid was highly sterile. The other wild species, C' reticulatum, was crossed readily with the cultivated chickpea. Meiosis of the hybrids, involving 4 different C. arietinum lines, was normal, and they were fertile. This wild species therefore can be considered as the wild progenitor of the cultivated chickpea.     

Major flowering time gene and polygene effects on chickpea seed weight

The effect of the major flowering gene (PPD) on seed weight of chickpea was studied on 450 F₃ families from reciprocal crosses between a small‐seeded, early‐flowering (PPD/PPD) type and a large‐seeded, late flowering (PPD/PPD) cultivar. F₄ progeny tests were carried out to determine the PPD genotypes of each individual F₃. The effects of the PPD gene and the polygenes on mean seed weight were both significant. Genetic correlations between time to flowering and seed weight were positive and relatively high, suggesting that in certain genetic backgrounds it might be difficult to breed early‐flowering cultivars without compromising seed weight.     

Leaf shape × sowing density interaction affects chickpea grain yield

Modifying plant architecture is considered a promising breeding option to enhance crop productivity. Modern chickpea (Cicer arietinum L.) cultivars with either compound (wild‐type) or simple leaf shapes are commercially grown but the relationships between leaf shape and yield are not well understood. In this study, a random sample of ‘Kabuli’ type progeny lines of both leaf types, derived from two crosses between modern American simple leaf cultivars and early‐flowering wild‐type breeding lines, were planted at different sowing densities. Leaf area development and final grain yield in genotypes of the two leaf types responded differently to changes in sowing densities. Compound leaf lines attained higher leaf area indices and higher grain yields at both low and high sowing densities. Yield responses of the simple leaf lines to increasing sowing density were significantly higher compared to compound leaf genotypes in two of three field experiments. The prospects for utilizing the simple leaf trait as a breeding target for short‐season growing areas are discussed.     

Two new traits - open flower and small leaf in chickpea (Cicer arietinum L.)

Two new traits – open flower and small leaf in chickpea are discussed. Open flower, a natural mutant in a good agronomic background is reported for the first time, small leaf trait has been reported earlier, and has now been studied by breeders. Both useful traits were found to be monogenic recessive. The joint F₂ segregation data revealed no linkage between flower colour and flower type, but flower type and leaf size showed some linkage. Open flower could contribute to a higher rate of cross pollination and utilization of heterosis. The small leaf allows light to penetrate the crop canopy, and could be useful in designing a physiologically efficient plant type in chickpea. This revised version was published online in July 2006 with corrections to the Cover Date.     

Development of early-flowering Kabuli chickpea with compound and simple leaves

Terminal drought is a major constraint to chickpea (Cicer arietinum L.) production. Autumn sowing and early flowering have been suggested as ways to benefit from the winter rains in short rainy seasons under dryland cropping. High‐yielding, late‐flowering, simple‐leafed (slv/slv) chickpea cultivars with good field resistance to Ascochyta blight have been bred recently. Changing plant architecture, by altering leaf shape, may affect agronomic performance. As no information is available on the effect of leaf shape on phenology and seed yield, this study was aimed at: (i) introducing the simple leaf trait into an early‐flowering chickpea background; (ii) comparing the grain yield of the two leaf types in early vs. late flowering backgrounds and (iii) producing breeding lines combining early flowering, large seeds and Ascochyta tolerance with both leaf types. Hybrid progeny were studied from the cross of ‘Sanford’ (slv/slv) and ICC7344, (compound, SLV/SLV). Four early‐podding, F₈ breeding lines were selected with either simple or compound leaves. In three different field experiments under dryland conditions (334–379 mm), they yielded ca. 1.4 t/ha as compared with 1.0 t/ha in the standard Israeli ‘Yarden’ on one site, but no significant differences in yield were obtained in the other two experiments.     

Genetic Analysis of Developmental Traits in Chickpea

Chickpea (Cicer arietinum L.) is an important legume crop in India. The present study was conducted to investigate the inheritance of several developmental traits in three crosses of chickpea, viz., WFWG III’בT20’, ‘T88’בBold Seeded’, and ‘NP34’בP1528-1-1’, each having seven generations. The seven generations were P₁, P₂, F₁, B₁, B₂, F₂, and F₃. The experimental lay-out was randomized complete block design with three replications. Data were acquired on days to flowering (DF), days to maturity (DM), plant height in cm (PH), number of primary branches (PB), and number of secondary branches (SB). Generation mean analysis was used to estimate the genetic components; narrow sense heritability was estimated using variance components; and correlation analysis to estimate correlation coefficients among different traits. Genetic differences were found in all three crosses for all traits studied. Additive, dominance, and epistatic effects were found for many traits'. Duplicate epistasis was observed for all traits except number of PB. Higher order interactions and/or linkage were detected for DM and SB. For many traits the relative magnitudes of the genetic effects differed among crosses, thus the extrapolation to other crosses may be difficult. The inheritance becomes more complex as the fate of the character is decided at a later stage in the life cycle. Positive heterosis was observed for some traits, but the exploitation of this component may not Feasible since stable male sterile lines are not available. Early maturity and high yield ‘may be selected independently because of the absence of any significant correlation between these two traits.     

Allelic relationships of genes controlling number of flowers per axis in chickpea

Genetic variation for number of flowers per axis in chickpea (Cicer arietinum L.) includes single-flower, double-flower, triple-flower and multi-flower traits. A double-flowered (DF) line ICC 4929, a triple-flowered (TF) line IPC 99-18 and a multi-flowered (MF) line JGM 7 were intercrossed in all possible combinations and flowering behavior of parents, F₁s and F₂s was studied to establish allelic relationships, penetrance and expressivity of genes controlling number of flowers per axis in chickpea. The F₁ from ICC 4929 (DF) × IPC 99-18 (TF) cross were double-flowered, whereas F₁ from ICC 4929 (DF) × JGM 7 (MF) and IPC 99-18 (TF) × JGM 7 (MF) crosses were single-flowered. The F₂ from ICC 4929 (DF) × IPC 99-18 (TF) cross gave a good fit to a 3:1 ratio for double-flowered and triple-flowered plants. The F₂ from ICC 4929 (DF) × JGM 7 (MF) cross segregated in a ratio of 9:3:3:1 for single-flowered, double-flowered, multi-flowered and double-multi-flowered plants. The F₂ from IPC 99-18 (TF) × JGM 7 (MF) cross segregated in a ratio of 9:3:4 for single-flowered, triple-flowered and multi-flowered plants. The results clearly established that two loci control number of flowers per axis in chickpea. The double-flower and triple-flower traits are controlled by a single-locus (Sfl) and the allele for double-flowered trait (sfl ^d ) is dominant over the allele for triple-flower trait (sfl ^t ). The three alleles at the Sfl locus has the dominance relationship Sfl > sfl ^d > sfl ^t . The multi-flower trait is controlled by a different gene (cym). Single-flowered plants have dominant alleles at both the loci (Sfl_ Cym_). The double-flower, the triple-flower and the multi-flower traits showed complete penetrance, but variable expressivity. The expressivity was 96.3% for double-flower and 76.4% for double-pod in ICC 4929, 81.2% for triple-flower and 0.0% for triple-pod in IPC 99-18, and 51.3% for multi-flower and 24.7% for multi-pod in JGM 7. Average number of flowers per axis and average number of pods per axis were higher in JGM 7 than double-flowered line ICC 4929 and triple-flowered line IPC 99-18. The results of this study will help in development of breeding strategies for exploitation of these flowering and podding traits in chickpea improvement.     

Reciprocal cross differences in a 6×6 diallel set of groundnut (Arachis hypogaea L.) in the F1 generation

Summary Reciprocal cross differences were studied in a 6×6 diallel full set comprising of thirty hybrid combinations of groundnut in the F₁ generation.Reciprocal cross differences were observed for growth habit in four pairs of crosses, for leaf colour, flower colour and stem pigmentation in two pairs of crosses each. It was observed that the inheritance of flower colour, stem pigmentation and testa colour which exhibited different shades of purple colour was likely to be governed by pleiotropic gene(s). Among the quantitative characters significantly positive reciprocal effects were observed in different crosses for number of mature pods per plant, weight of pods per plant and shelling percent. Marked reciprocal cross differences were observed for pod and kernel characters like pod filling, pod beak, pod constriction and testa colour.     

Molecular mapping and characterization of an RGA locus RGAPtokin1-2 171 in chickpea

Resistance gene analog polymorphism (RGAP)is a targeted homology based method, which has been used in different crops to identify tightly linked markers for disease resistance genes and also to enrich the map with a different class of markers. In chickpea, using the RGA primers, which are designed based on the conserved motifs present in characterized R-genes, Bulk Segregant Analysis (BSA) was performed on a resistant bulk and a susceptible bulk along with parents for ascochyta blight resistance. Of all available RGAs and their48 different combinations, only one RGA showed polymorphism during BSA. This marker was evaluated in an F_7:8 population of142 RILs from an interspecific cross ofC. arietinum (FLIP 84-92C) × C. reticulatum (PI 599072) and was mapped toCicer linkage map. The genomic location of chickpea RGA was compared with the locations of mapped chickpea R-genes. This is the first RGA marker mapped to chickpea linkage map. This revised version was published online in August 2006 with corrections to the Cover Date.