Inheritance of trichomes and resistance to pod borer (Helicoverpa armigera) and their association in interspecific crosses between cultivated pigeonpea (Cajanus cajan) and its wild relative C. scarabaeoides

The legume pod borer, Helicoverpa armigera, is one of the most devastating pests of pigeonpea. High levels of resistance to pod borer have been reported in the wild relative of pigeonpea, Cajanus scarabaeoides. Trichomes (their type, orientation, density and length) and their exudates on pod wall surface play an important role in the ovipositional behavior and host selection process of insect herbivores. They have been widely exploited as an insect defense mechanism in number of crops. In the present investigation, inheritance of resistance to pod borer and different types of trichomes (A, B, C and D) on the pod wall surface in the parents (C. cajan and C. scarabaeoides) and their F₁, F₂, BC₁ (C. cajan × F₁), and F₃ generations has been studied. Trichomes of the wild parents (high density of the non-glandular trichomes C and D, and glandular trichome B and low density of glandular trichome A) were dominant over the trichome features of C. cajan. A single dominant gene as indicated by the segregation patterns individually will govern each trait in the F₂ and backcross generation. Segregation ratio of 3 (resistant): 1 (susceptible) for resistance to pod borer in the F₂ generation under field conditions was corroborated with a ratio of 1:1 in the backcross generation, and the ratio of 1 non-segregating (resistant): 2 segregating (3 resistant: 1 susceptible): 1 non-segregating (susceptible) in F₃ generation. Similar results were obtained for pod borer resistance under no-choice conditions. Resistance to pod borer and trichomes associated with it (low density of type A trichome and high density of type C) are governed individually by a dominant allele of a single gene in C. scarabaeoides. Following backcrossing, these traits can be transferred from C. scarabaeoides into the cultivated background.     

Inheritance of duration from sowing to first flowering in pigeonpea

Duration from sowing to flowering is the most important trait influencing adaptation in pigeon pea (Cajanus cajan), but the inheritance of this trait has not been elucidated clearly. Crosses were made between two early (60 to 70d) and one late (160 to 170d) flowering pigeonpea genotype and F₁, F₂ and BC₁ populations produced. These populations, comprising 60 to 100 parents, 30 F₁, 400F₂ and 40 to 50 BC₁ plants, were grown under natural (mean13.4 hd^-1) and artificially extended (to 15 hd^-1) daylength and duration from sowing to first flowering recorded. Genetic analysis of the segregation ratios, supported by Chi-square tests, indicated that the duration from sowing to flowering in each of the crosses was controlled by two genes assorting independently and with predominantly additive quantitative effects. The segregation patterns were most clearly defined in the 15 hd^-1 daylength. This revised version was published online in July 2006 with corrections to the Cover Date.     

Inheritance of yield and yield-related traits in highland maize hybrids of Uganda

Although many studies have been conducted on gene action of grain yield and yield related traits in maize, none of them focused on highland maize in Uganda. This study was conducted to establish the gene action controlling inheritance of yield and its related traits in highland maize hybrids. Thirty-six F₁ hybrids generated from a 9 x 9 half diallel mating design, were planted with two local checks in three highland locations; Kalengyere, Kachwekano, and Buginyanya with two replications using a 2 x 19 alpha (0, 1) lattice design. Results showed that inheritance of ear length and anthesis-silking interval was controlled by both additive and non-additive gene action while the inheritance of days to anthesis, days to silking was mainly controlled by additive gene action. The inheritance of grain yield and other yield related traits was greatly influenced by environment and genotype x environment interaction. Considering the great influence of the environment and genotype x environment interaction on most of the traits including grain yield, further testing in additional locations over more seasons and broadening the genetic base of the parents is encouraged.     

Inheritance of resistance to two isolates of sterility mosaic pathogen in pigeonpea (Cajanus cajan (L.) Millsp.)

The resistant reaction to tomato spotted wilt virus (TSWV) was found to be determined by a single dominant gene in three Capsicum chinense Jacq. accessions (‘PI 152225’, ‘PI 159236’, ‘7204’). Allelism studies indicated that all C. chinense lines bear the same allele located at the Tsw locus. All the inoculated plants in the allelism tests displayed a resistant hypersensitive phenotype characterized by necrotic local lesions followed by abscission of the inoculated organ. However, a small proportion of them showed late systemic infection. Nine TSWV isolates obtained from these individual plants with systemic symptoms were backinoculated to the three resistant parents. All isolates were able to infect systemically all the resistant accessions without inducing local necrotic lesions. Serological analysis confirmed that these nine viral isolates belong to the TSWV species (serogroup I). Consequently, the susceptible plants in the allelism tests could not be interpreted as possessing a recombinant genotype because of the virulence change in the viral strain. Hobbs et al. (1994) already reported the existence of TSWV pathotypes overcoming the resistance of C. chinense resistant accessions. Practical consequences for pepper breeding associated with the emergence of these resistance-breaking isolates are discussed. This revised version was published online in July 2006 with corrections to the Cover Date.     

Construction of a linkage map and identification of DNA markers linked to Fom-1, a gene conferring resistance to Fusarium oxysporum f.sp. melonis race 2 in melon

Resistance to Fusarium oxysporum f.sp. melonis race 2 is conferred by a single dominant gene, Fom-1 in melon. Here, we identified DNA markers tightly linked to Fom-1 that could be used for marker assisted selection in breeding programs. First, we developed 125 F₂ plants derived from the cross between melon lines P11 (fom-1fom-1) and MR-1 (Fom-1Fom-1). Using the F₂ population, we constructed a linkage map including 14 SSR markers which had not been mapped previously. Fom-1 was confirmed to be allocated to linkage group 7. Then, we identified four AFLP markers using bulked segregant analysis. The AFLP marker TAG/GCC-470 was completely linked to Fom-1 and other three markers were mapped near Fom-1. TAG/GCC-470 and TCG/GGT-400 were respectively converted to STS and CAPS markers. Usefulness of DNA markers was confirmed in the analysis with several melon cultivars and lines.     

Genetics of resistance to P3 isolate of Phytophthora blight in pigeonpea

Seedlings from six crosses between susceptible × resistant and two between susceptible parents were screened against P₃ isolate of Phytophthora drechsleri f. sp. cajani in the glasshouses. Disease reaction was scored on a rating scale of 1–5. Resistance was found to be controlled by one dominant gene and some minor genes and is affected by ontogeny. The resistance gene appeared to be different from the one reported earlier (Pd₁) and is designated here as Pd₃. This revised version was published online in July 2006 with corrections to the Cover Date.     

Inheritance of resistance to Pyrenochaeta lycopersici in tomato

Summary Tomato accessions (Lycopersicon sp.), along with commercial cultivars and breeding lines were grown in a field infested with the brown root rot (BRR) organism, Pyrenochaeta lycopersici and evaluated for resistance. Three L. esculentum Mill. accessions, P.I. 260397, P.I. 262906 and P.I. 203231, were resistant and were used as male parents in crosses designed to transfer resistance to tomatoes of fresh market type. Through analysis of parental generations and F₁ and F₂ progenies from three crosses the heritability of resistance in the broad sense was estimated to range from 25 to 43 percent. The minimum number of genes influencing resistance was estimated to be from 4 to 8.Florida Agricultural Experiment Stations Journal Series Paper no. 317.     

Inheritance of agriculturally important traits in mango

Summary High heterozygosity on the one hand, and the inability to carry out successful hand pollinations on the other hand, have limited the amount of systematic work which has been done in mango breeding. In studying the inheritance of important horticultural traits we must first analyse the distribution of different traits in seedlings derived from open pollination. We studied correlations between these traits and assessed the contribution of the three female parents to that distribution.Although in general the trait distribution pattern is similar among the three progenies, some differences were noted. We also detected some correlations among various traits which might be useful for future breeding. It was concluded from both a chi-square test and an intraclass correlation coefficient that there is a specific female parent effect on both harvest season and fruit color; a smaller effect was found on fruit taste and size, and no effect of the female parent tree was detected on the distribution of both the juvenile period and fertility.     

Inheritance of resistance to Ascochyta blight in chickpea

Summary The mode of inheritance of resistance to Ascochyta blight (Ascochyta rabiei) isolate G-52 in chickpea was studied in three cross combinations and their reciprocals. It was found that resistance variety I-13 was controlled by a single dominant gene pair.     

Inheritance of resistance to yellowberry in durum wheat

Resistance to grain yellowberry in durum wheat (Triticum durum Desf.) was investigated using generation mean analysis in four resistant or intermediate-resistant X susceptible crosses. Significant differences in resistance were observed between generations in all crosses. Generation mean analysis indicated a complex gene action controlling this trait, with additive, dominance and epistatic effects. Additive (d) components were positive in all crosses, suggesting that additive effects contributed more to resistance than to susceptibility. In contrast dominance (h) effects were negative in majority of crosses. The minimum number of genes controlling resistance was estimated at 1.41. Mid-parent heterosis ranged from 28.5 to 52.1 indicating dominance of resistance. Broad-sense heritability estimates ranged from 0.52 to 0.88, while narrow-sense heritability estimates ranged from 0 to 0.79. Estimates of genetic gain for resistance ranged from low to high. Estimates of broad and narrow sense heritabilities indicated that genetic effects were larger than environmental effects. Additive effects represented the largest components of genetic effects.     

Inheritance of resistance to fusarium wilt in chickpea

This preliminary study indicated that the resistance to race 2 of fusarium wilt is controlled by two genes, the first of which must be present in the homozygous recessive form, and the other in the dominant form, whether homozygous or heterozygous for complete resistance. Early wilting results if the other gene is homozygous recessive. Late wilting occurs if both loci are dominant. The existence of differences among chickpea cultivars in the time taken to express the initial symptoms of fusarium wilt were observed.     

Inheritance of yield components and yield in relation to evidence for heterosis in F1 barley hybrids

Summary Yield components and yield were studied in F₁ barley hybrids produced by hand pollination or male sterility. Grain number exhibited only partial dominance but grain weight showed dominance or overdominance and contributed to the heterotic situation particularly in 2×6-row crosses. For the commercial exploitation of heterosis it is essential that hybrids should be found which show greater dominance for high grain number.     

Inheritance and relationships of important agronomic traits in almond

The inheritance of 16 important agronomic traits and its relationship were studied for four years in a population of 167 almond [P. dulcis (Mill.) D.A. Webb] seedlings obtained from a cross between the French selection ‘R1000’ (‘Tardy Nonpareil’ × ‘Tuono’) and the Spanish cultivar ‘Desmayo Largueta’. For some traits (blooming and leafing date) descendants segregated between the value of both progenitors, meanwhile for others the mean of the offspring was lower (bloom density, productivity and ripening date) or higher (in-shell/kernel ratio and double kernels). As expected, kernel bitterness and self-incompatibility behaved as monogenic traits. Some important correlations between traits were detected. The implications of the transmission and the correlation of these traits in the breeding programmes are discussed.     

Inheritance of some morphological traits in grain amaranthus

Summary Intraspecific crosses involving five cultivars of Amaranthus hypochondriacus and two from A. caudatus were studied to investigate the inheritance of five morphological traits (seed coat colour, inflorescence colour, seedling colour, oval leaf mark and purple leaf mark). Seedling colour, inflorescence colour, seed coat colour and oval leaf mark segregated to a 3:1 ratio and therefore each was controlled by a single dominant gene. The purple leaf mark segregated in 9:7 ratio and hence may be controlled by two dominant genes. Simultaneous segregation for seed coat colour and inflorescence colour gave a ratio of 9:3:3:1. Similar genetic ratio was observed for the simultaneous segregation for oval leaf mark and inflorescence colour. It was suggested that each of these traits is controlled by independent genes.     

Inheritance of resistance to Phytophthora fragariae Hickman in strawberry

Summary It has been found that complete resistance of the strawberry cultivars and selections Earliglow, Guardian, MdUS 2700, MdUS 2929, MdUS 3816 and Redchief to Phytophthora fragariae is inherited in a one-to-one ratio, suggesting that these genotypes have one major resistance gene effective to the races present in the test field.The high level of partial resistance of Cambridge Favourite has clearly been recovered in its progenies. However, from results presented here, no conclusions could be drawn with regard to the number of genes involved in the partial resistance of Cambridge Favourite. It is, however, suggestive that about half the susceptible selections derived from crosses with Cambridge Favourite have shown a relatively high level of partial resistance. The selections concerned were obtained by selection on horticultural characters in seedling populations planted on an uninfested field.     

Inheritance of partial resistance to Myzus persicae in lettuce

Summary The genetics of partial resistance of lettuce to Myzus persicae was studied using F₁ and F₂ generations of two crosses between a susceptible and partially resistant accession (Norden x Batacer and Liba x Norden) and three crosses in which both parents were partially resistant (Batavia la Brillante x Batacer, Batacer x Liba and CGN4741 x Batacer). Partial resistance to M. persicae inherited quantitatively, without important dominance effects. Only in the cross Batacer x Liba were significant departures of the F₁ and F₂ from the midparent found, which were probably caused by epistatic effects. Reciprocal F₁s had similar resistance levels, indicating the absence of cytoplasmic or other maternal effects. Estimates of broad-sense heritability ranged from 0.34 to 0.61. The results indicated that lines with an improved resistance level can be obtained from crosses between partially resistant accessions, preferably by line selection or the application of indirect marker aided selection.Abbreviations PR partial resistance, partially resistant - S susceptibility, susceptible     

Inheritance of resistance to Russian wheat aphid in barley

Summary The inheritance of resistance to Russian wheat aphid Diuraphis noxia (Mordvilko), in two resistant barleys, Hordeum vulgare L., ASE/2CM//B76BB and Gloria/Come, was studied in the field and in the greenhouse. The resistant genotypes were crossed with susceptible genotypes Esperanza and Shyri. Resistance reactions of F1, BC1, and F2 plants, and individual F2 plant derived F3 families indicated that resistance in each genotype was controlled by the same single dominant gene.     

Inheritance of adult-plant resistance to Phytophthora capsici in pepper

Summary Inheritance studies were conducted to determine the genetic basis of adult-plant resistance in pepper (Capsicum annuum L.) to Phytophthora capsici. F₁, backcrosses and F₂ populations were developed using the resistant parent Criollo de Morellos 334 and susceptible parents Agronômico 10-G and Yolo Wonder. Pepper plants, at 36 days post-emergence, were inoculated near the base of the stem with an inoculum suspension of 5×10⁴ zoospores/ml. Segregation ratios in the F₂ generation of 13 resistant to 3 susceptible plants fit a 2-gene model for resistance with dominant and recessive epistasis.     

Inheritance of resistance to four cucurbit viruses in Cucurbita moschata

Cucurbita moschata cv. Nigerian Local has been used as a source of resistance to Zucchini yellow mosaic virus (ZYMV), Watermelon mosaic virus (WMV), Papaya ringspot virus W (PRSV-W) and Cucumber mosaic virus (CMV) in breeding both Cucurbita moschata and Cucurbita pepo. We used the F₁, F₂ and BC₁ generations derived from the cross C.-moschata cv. Waltham Butternut × Nigerian Local to study the inheritance of resistance to each of the viruses. We confirmed monogenic dominant resistance to ZYMV previously attributed to Zym, and we report monogenic dominant resistance to WMV and CMV which we propose to designate Wmv and Cmv, respectively. A single recessive gene, which we propose to designate prv, controls resistance to PRSV. DNA samples were extracted from a Waltham Butternut BC₁ F₁ population screened with ZYMV and analyzed using randomly amplified polymorphic DNA markers. No RAPD markers linked to ZYMV resistance were found. This revised version was published online in July 2006 with corrections to the Cover Date.