Studies on the inheritance of root color and carotenoid content in red × yellow and red × white crosses of carrot,Daucus carota L.

Summary In red × yellow crosses of carrot (Daucus carota L.) three major genes were found to be segregating: Y ₂, inhibiting the synthesis of carotenoids, L, stimulating lycopene synthesis and A ₁, the action of which was not very clear. It is assumed that the dominant allele A ₁ enhances the formation of beta- and alpha-carotene at the expense of lycopene resulting in a more orange color instead of red, however, minor genes, modifiers and various interactions were obviously also involved.At least two inhibitor genes (Y and Y ₂) were segregating in red × white crosses. Evidence was found for a third inhibitor gene (Y ₁) in some crosses but this was not clear-cut.In F₂ progenies of red × white crosses a new phenotype was detected, i.e. tinge yellow-red, the xylem of which had a higher total carotenoid content than the phloem. Nothing is yet known about the genetics of this phenotype; tentatively it is suggested that one of the Y-genes might be less effective in the xylem than in the phloem regarding the suppression of lycopene synthesis.Much variation in pigment composition was found in F₂ generations of red × yellow and red × white crosses. Lycopene and beta-carotene were the predominant pigments in red and orange roots; zeta-carotene and phytofluene were generally shown to be present in smaller amounts while the presence of gamma-carotene and neurosporene could only be demonstrated in a limited number of roots. White and yellow roots were low in total carotenoids and consequently no or only a few specific carotenoids were detected in these roots.Research supported by the College of Agricultural and Life Sciences and by a grant from the Campbell Soup Company, Camden, New Jersey. The investigation is a portion of a thesis submitted in 1978 as partial fulfillment of the requirements of the PhD degree.     

Investigations on the inheritance of color and carotenoid content in phloem and xylem of carrot roots (Daucus carota L.)

Summary Investigations on the inheritance of root color in carrot (Daucus carota L.) were carried out by crossing uniformly colored roots to various tinge type roots, i.e. roots of which the xylem differs in color from the phloem.A single major gene (Y) was found to be responsible for the observed differences in progenies of orange x tinge orange-white (orange referring to phloem color, white to xylem color) crosses. Plants carrying the dominant Y-allele had either white or tinge orange-white roots, whereas plants with orange roots were of the genotype yy. Similarly one major gene (Y ₂) determined the segregation found in progenies of orange x yellow crosses. In the latter crosses, plants having the dominant Y ₂-allele had either yellow or tinge orange-yellow roots while the recessive would be orange. Variation in phloem color, i.e. differences between white and tinge orange-white or between yellow and tinge orange-yellow, was apparently caused by minor genes, modifiers, gene interactions, or by genes that are not involved in carotenogenesis in a direct way.When both the Y- and Y ₂-genes were present, the roots were always white. Usually white roots gave a digenic segregation pattern in the F₂ when crossed to orange, but there was some evidence that a third gene (Y ₁) was segregating in some crosses. Tinge orange-white x yellow crosses gave approximately the same results as orange x white crosses, confirming that the same Y- and Y ₂-genes were segregating.In crosses between orange lines and a light yellow line (RY) certain F₁ 's appeared to have a light orange xylem and a fairly dark orange phloem, which seems to be some evidence for the existence of recessive yellow. Although almost nothing is known yet about the genetics of RY it is assumed that it still carries a dominant inhibitor gene which may be leaky in heterozygous condition. The value of such a line as an aid in the selection of superior orange lines is discussed.Alpha- and beta-carotene were found to be the major pigments in orange carrot tissue; phytofluene, zetacarotene, gamma-carotene and xanthophylls were shown to be present in smaller amounts. Besides xanthophylls and a small amount of beta-carotene dark yellow carrot tissue appeared to contain an appreciable amount of an unidentified pigment (pigment I). Light yellow and white phloem or xylem tissue were low in total carotenoids.Research supported by the College of Agricultural and Life Sciences and by a grant from the Campbell Soup Company, Camden, New Jersey, USA. The investigation is a portion of a thesis submitted in 1978 as partial fulfillment of the requirements of the PhD degree.     

Chimerical structure and carotenoid inheritance in Chrysanthemum morifolium (Ramat.)

Summary Progeny analysis showed that yellow-flowered chrysanthemum sports with carotenoid only in L1 are indistinguishable from their white progenitors in breeding behaviour; those with carotenoid in L2 breed quite differently. Chimerical structure has, therefore, to be considered when analysing flower colour inheritance data. Segregations were consistent with the action of the single dominant gene I. Such simply inherited characters may be useful in studies to distinguish between the several alternative patterns of inheritance which can be suggested in the species.     

Inheritance of resistance to two races of sunflower downy mildew (Plasmopara halstedii) in two Helianthus annuus L. lines

Sunflower downy mildew caused by Plasmopara halstedii is an important disease of sunflower capable of causing losses of more than 80% of production. Races 100, 300, 310, 330, 710, 703, 730 and770 of the fungus have been identified in Spain. Race 703, of high virulence, has been identified frequently in the northeast, while race 310 seems to occur over the south, the main sunflower growing region of the country. Oil sunflower lines RHA-274 and DM4 were studied for their resistance to races 310(RHA-274 and DM4) and 703 (DM4). In each cross, only one plant of the resistant parent was crossed to the inbred susceptible line HA-89 (or cmsHA-89).Plants from F₂ and backcross(BC₁F₁ to susceptible parent)generations were evaluated for fungal sporulation on true leaves and/or cotyledons. The resistant-to-susceptible ratios obtained in the F₂ and BC₁F₁ progenies from the crosses cmsHA-89 × RHA-274 and HA-89 × DM4suggested that one major gene in each line is responsible for resistance to race 703.The segregations of the progenies of the cross HA-89 × DM4 inoculated with race 703also fitted the ratios 1:1 and 3:1 (for BC₁F₁ and F₂, respectively)corresponding to control of resistance by a single dominant gene. In RHA-274, the gene for resistance to race 310 was designated Pl ₉, whereas Pl _v is tentatively proposed to designate the gene in DM4 responsible for resistance to races310 and 703. This revised version was published online in August 2006 with corrections to the Cover Date.     

Inheritance of flower pigments in tulip (Tulipa L.)

Summary In order to investigate the inheritance of flower colour in tulips, seven cultivars were crossed and selfed in a diallel. Of these parents and their F₁'s the relative amounts of carotenoids, delphinidin, cyanidin, pelargonidin, quercetin and kaempferol were determined.For delphinidin, quercetin and daempferol only additive gene action was determined, and for carotenoids, cyanidin and pelargonidin also non-additive gene action and plasmic differences.Biosynthesis of delphinidin and pelargonidin was only found when cyanidin was present, while synthesis of delphinidin and pelargonidin was antagonistic.     

Inheritance of β-carotene concentration in durum wheat (Triticum turgidum L. ssp. durum)

Despite being one of the important characteristics in determining pasta quality in durum wheat (Triticum turgidum ssp. durum), there is no direct report on inheritance of β-carotene concentration. The objectives of this study were to determine the inheritance of β-carotene concentration and the number of genes involved in six crosses of durum. For the cross PDW-233 (P₁) × Bhalegaon-4 (P₂), F₁, F₂, BCP₁ and BCP₂ populations were developed. For all other crosses, only the F₁ and F₂ populations were developed. β-carotene concentration was determined for all populations and parents of each cross grown at Hol, Maharastra, India. The cross PDW-233 × Bhalegaon-4 was also evaluated at Dharwad, Karnataka, India. Low β-carotene concentration was partially dominant in most of the crosses. Broad sense heritability was 67 and 91% at Dharwad and Hol, respectively, for the cross PDW-233 × Bhalegaon-4 and varied from 74 to 93% for the other five crosses indicating the presence of additive gene effects. The frequency distributions of the trait in the F₂ populations were not normal and were skewed towards the lower parent. Segregation of β-carotene concentration in the six F₂ populations indicated that at least two major genes and two or three minor genes with modifying effects govern the trait. Analysis of variance indicated that environment had comparatively little influence on the trait and this should allow for easy selection. The joint scaling test revealed additive × additive, additive × dominance and dominance × dominance epistatic interactions in the cross PDW-233 × Bhalegaon-4. These authors contributed equally.     

Superior performance of two homozygous diploid lines from naturally occurring polyhaploids in oilseed rape (Brassica napus)

Summary Homozygous diploids in oilseed rape were produced by pipetting drops of 0.1 per cent colchicine into the leaf axils of rooted cuttings from naturally occurring polyhaploids after removing the waxy covering with a scalpel. Trial results from spring and winter rape showed that occasional homozygous diploid lines yielded consistently more oil per ha than the parental varieties. Prospects for breeding oilseed rape as a self-fertilised crop are discussed.     

Control and inheritance of resistance to yellow rust in Triticum aestivum-Lophopyrum elongatum chromosome substitution lines

A set of T. aestivum-L. elongatum chromosome substitution lines was tested for yellow rust resistance at the seedling stage. Inheritance of the resistance and esterase-5 (Est-5) variation were studied. The results demonstrated that L.elongatum carried a new gene(s) conferring yellow rust resistance. This gene was dominant and located on chromosome 3E of L. elongatum. The biochemical locus encoding Est-5was also located on chromosome 3E, and co-segregated with theYr gene(s) in the wheat background. The transmission frequencies of chromosome 3E in 3E(3A) × CS, 3E(3B) × CS and 3E(3D) × CS hybrids were scored.None of the hybrids transmitted the alien chromosome at thetheoretical maximum rate, but the transmission frequencies ofchromosome 3E in F₂ populations of 3E(3A) × CS and 3E(3D) × CS were significantly higher than in thatof 3E(3B) × CS.     

Genetic analysis of inbred lines and their crosses for resistance to head blight (Fusarium culmorum,F. graminearum) in winter rye

Summary For genetic analysis of head blight in winter rye (Secale cereale) caused by Fusarium culmorum, six homozygous inbred lines from the Petkus gene pool were crossed in all combinations to obtain 15 diallel F₁ crosses and the corresponding 15 F₂ crosses. These materials and 10 additional inbreds were artificially inoculated in a 2-year field experiment. The inbreds were also tested with F. graminearum in a separate sub-experiment.Single disease rating, average disease rating, and yield components (grain-weight per spike, 1000-grain weight, kernel number per spike) relative to the non-inoculated treatment were significantly affected by Fusarium head blight in all material groups. The relative grain weight per spike ranged from 26% to 88%. Significant genotypic and genotype x year interaction variances were found throughout. Heritabilities were highest for homogeneous inbreds (h²=0.6–0.8) and lowest for heterogeneous F₂ crosses (h²=0.4–0.6). Disease rating and relative grain-weight per spike were highly correlated for the inbreds and F₂ crosses (r0.7, P0.01), but lower for the F₁ crosses (r0.6, P0.05). Inter-annual correlation coefficients for disease ratings and relative grain-weight per spike ranged from r0.7 (inbreds) to r0.5 (F₂ crosses). The diallel analysis showed significant GCA effects only for relative 1000-grain weight in 1990, but significant SCA and SCAx year interaction variances for most traits. The resistances of 16 inbreds to F. culmorum and F. graminearum were tightly associated for all traits (r=0.96–0.97, P0.01).In conclusion, only slow progress can be expected from selecting for Fusarium head blight resistance in rye due to the limited amount of additive genetic variance and the great improtance of environmental factors.     

Inheritance of isozyme variants and their linkage relationships in Chinese fir (Cunninghamia lanceolata Hook.)

Summary 49 single-clone seed samples of Chinese fir (Cunninghamia lanceolata) were used to investigate genetic variation for nine enzyme systems. LAP, PGM, and SOD were invariant, whereas GDH, GOT, IDH, MDH, 6PDH, and SKDH were highly variable. Inheritance patterns of the variable enzyme systems were mostly in accordance with Mendelian expectations. Linkage was studied by analysing 43 two-locus combinations with the following two-locus combinations significantly linked in at least 50% of the respective double-heterozygous clones: Gdh1: Got3; Gdh1: Idh1; Got2: 6Pdh2; Idh2: Skdh1; Mdh1: 6Pdh1. Estimates of recombination frequencies for each locus pair varied considerably among clones.Supported by the Carl Duisberg Gesellschaft.     

Postulation of resistance genes to yellow rust in wild emmer wheat derivatives and advanced wheat lines from Nepal

Summary Seedlings of 38 wild emmer derivatives, and a total of 53 advanced wheat varieties/lines introduced from the International Maize and Wheat Improvement Centre (CIMMYT) or other sources, Nepalese breeding lines and local cultivars were inoculated with 18 different yellow rust isolates to postulate yellow rust resistance genes (Yr). Many wild emmer wheat derivatives used were resistant to all isolates indicating the presence of undescribed genes. Some derivatives carried Yr9, Yr6 and/or YrSU. Genes Yr1, Yr2, Yr6, Yr7, Yr8, Yr15, YrSU and YrA+ are no longer effective in Nepal; Yr4, Yr5, Yr9, Yr10, YrSP and YrSD are still effective; the effectiveness of Yr3 remains unclear. This study shows that stripe rust resistance in seedling stage of most Nepalese cultivars and advanced materials is based on Yr9 with combinations of Yr2, Yr6, Yr7, and YrA+, of which only Yr9 is still effective in Nepal. In many countries Yr9 has lost its effectiveness. Therefore the introduction of new Yr-genes from wild emmer wheat in Nepalese cultivars is highly important.     

Expression of barley yellow dwarf virus and Russian wheat aphid resistance genes in and fertility of spring wheat × triticale hybrids and backcross lines

Summary The Barley Yellow Dwarf Virus disease (BYDV) and the Russian wheat aphid (RWA) Diuraphis noxia (Mordvilko) have caused significant losses to wheat and barley in several areas of the world. Important sources of resistance to both BYDV and RWA have been found in Triticale. Different generations of interspecific wheat x Triticale crosses were produced and the progenies were screened for BYDV and RWA tolerance. Plants with equal chromosome numbers showed different levels of fertility. A significant correlation was observed between pollen fertility and seed set in primary florets (r=0.57). In generaL, pollen fertility, seed set and the number of euploid plants (2n=42) increased from one generation to the next. The expression of BYDV tolerance varied from population to population. Additive effects were predominant in F₁ and some backcross populations. A dominant effect of rye tolerance genes was also observed in few populations. A monogenic trait or a quantitative (polygenic) character would not agree with the observed segregation patterns. The heritability of this oligogenic tolerance was quite different between populations and in many populations the tolerance genes were only partially expressed. Some transgressive segregation for tolerance and sensitivity was demonstrated. The genes controlling tolerance to RWA in Triticale lines, Muskox 658 and Nord Kivu were not expressed in advanced lines resistant to BYDV. This indicates that tolerance genes for BYDV and RWA in these lines are located on different chromosomes.     

Resistance to cane spot (Elsinoë veneta) in the red raspberry and its relationship to resistance to yellow rust (Phragmidium rubi-idaei)

Summary Varying degrees of resistance to cane spot were recorded among red raspberries in two cultivar trials and in 15 segregating families. The inheritance of resistance was studied, and the effect of gene H which determines the presence of cane hairs was assessed in eight of the families. The 0 to 5 scale used to record disease incidence was found to approximate to a logarithmic scale for the range of 0 to 93 cane spots per cane. Gene H and h phenotypes averaged scores of 3.05 and 2.42 respectively, but other genes independent of these had more influence on resistance. The latter genes appeared to be largely dominant. The possibility is discussed that one of them was a major gene with a large effect, but the evidence was equivocal in the absence of discontinuity in the expression of resistance. Resistance to yellow rust was studied in five of the families and was highly correlated with resistance to cane spot. Gene H had more influence on this disease, the mean counts of telia per unit leaf area for H and h segregates being 17.1 and 4.1 respectively.     

Worldwide distribution of β-amylase thermostability in barley

The thermostability of β-amylase in 6752 lines of worldwide barley genetic resources were investigated. Most of the lines were classified into high (type A), medium (type B) , and low (type C) thermostability. Subsequently the geographical distribution of these types was clarified. About 90% of the East Asian (Japan, the Korean Peninsula, China) lines were type A. More than 95% of Ethiopian barley was type C. The thermostability types of varieties in the western areas (north Africa, southwest Asia, Turkey, Europe) consisted of types A, B and C. These results suggest that there is a clear geographical differentiation in β-amylase thermostability, especially in East Asia and Ethiopia. The phenotype characteristics of each thermostability type line reflected the geographical differentiation. Besides types A, B and C, we found new thermostability types, including such useful mutants as a β-amylase-less mutant and highly-thermostable mutants than type A in both China and Nepal. This revised version was published online in August 2006 with corrections to the Cover Date.     

Genetical relationships between reactions to bacterial leaf spot,yellow mosaic and Cercospora leaf spot diseases in mungbean (Vigna radiata)

Summary Studies on the inheritance pattern of bacterial leaf spot (BLS), yellow mosaic (YM) and Cercospora leaf spot (CLS) reactions in crosses of BLS and YM resistant/tolerant but CLS susceptible × CLS resistant but BLS and YM susceptible parents indicated that resistances to BLS and CLS were governed by single dominant genes, whereas YM tolerance was a monogenic recessive character. The studies also indicated that these three genes were inherited independently. The simple inheritance pattern and independent assortment of the genes governing resistance/tolerance to these diseases suggest that the usual breeding methods will be adequate to develop multi-disease resistant mungbean cultivars.Paper XII in the series Studies on resistance in crops to bacterial diseases in India.     

Inheritance and allelic relationships of resistances to the Russian wheat aphid in two Iranian wheat lines

Russian wheat aphid (RWA), Diuraphis noxia (Kurdjumov), is a serious pest of small grains in many countries. A previous study screened 70 genotypes, collected from different parts of Iran, for RWA resistance. Four crosses were made between two resistant lines (Shz.W-102 and Shz.W-104) and two susceptible lines (Shz.W-101 and Shz.W-103). Parents, F₁, F₂, and BCF₁ seedlings were screened for RWA resistance in the greenhouse by artificial infection. To determine allelism, the two resistant lines were intercrossed and F₁, and F₂ seedlings were evaluated. Resistance in Shz.W-102 and Shz.W-104, when crossed with Shz.W-101, was controlled by one dominant gene. However, resistance in Shz.W-102 and Shz.W-104, when crossed with Shz.W-103, was controlled by two dominant genes. Genes in two resistant lines segregated independently of each other. A three-gene system was proposed to govern resistance in the lines under study . This revised version was published online in July 2006 with corrections to the Cover Date.     

Cytogenetical studies in wheat XIX. Location and linkage studies on gene Yr27 for resistance to stripe (yellow) rust

The stripe (yellow) rust resistance gene Yr27 was located in wheat (Triticum aestivum L.) chromosome 2B and shown to be closely linked to the leaf (brown) rust resistance genes Lr13 and Lr23 in the proximal region of the short arm. Gene Yr27 was genetically independent of Lr16, which is distally located in the same arm. While Yr27 was often difficult to score in segregating seedling populations, it is apparently quite effective in conferring resistance to avirulent cultures under field conditions. The occurrence of Yr27 in Mexican wheat germplasm and the current over-dependence on Yr27 for crop protection in Asia are discussed.     

Genetics of flower colour in China aster (Callistephus chinensis (L.) Nees)

Summary The genetics of flower colours violet, blue, deep pink, pink, light pink, creamy white and white was investigated in 17 cross combinations involving 10 parents in China aster (Callistephus chinensis (L.) Nees). Violet was dominant over all other colours; blue was dominant over creamy white; deep pink was dominant over pink and white, but incompletely dominant over light pink and pink was dominant over light pink and white. Four genes C, R, B and P were found to govern these different flower colours. The gene P had a dominant allele P^D and a recessive allele p.Contribution No. 146/88 of the Indian Institute of Horticultural Research, Bangalore 56080, India.