首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
M.K. Emami  B. Sharma 《Euphytica》2000,115(1):43-47
The inheritance of testa (seed coat) colour and interaction of cotyledon and testa colours were studied in seven crosses of lentil (Lens culinaris Medik.) involving parents with black, brown, tan or green testa and with orange, yellow or dark green cotyledons. Analysis of F2 and F3 seed harvested from F1 and F2 plants, respectively, revealed that although black testa is dominant over nonblack testa, its penetrance is not complete since both F1 plants and heterozygous F2 plants produced varying proportions of seeds with either black or nonblack testa. The F2 populations of the crosses between parents with brown and tan, as well as brown and green, testa segregated in the ratio of 3 brown : 1 tan and 3 brown : 1 green, respectively, indicating monogenic dominance of brown testa colour over tan or green. The expression of testa colour was influenced by cotyledon colour when parents with brown or green testa are crossed with those having orange or green cotyledons. Thus F2 seeds from these crosses with a green testa always had green cotyledons and never orange cotyledons. F2 seeds from these crosses with a brown testa always had orange cotyledons and never green cotyledons. These results suggest diffusion of a soluble pigment from the cotyledons to the testa. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

2.
The inheritance of siliqua orientation and seed coat colour in Brassica tournefortii was investigated using four genotypes varying in these two characters. The F1, F2 and backcross generations of two crosses were used for studying the segregation pattern of the traits. The plants were classified for seed colour as having brown or yellow seeds and for siliqua orientation as having upright, semi‐spread or spread siliqua. Seed colour was found to be under monogenic control with brown being dominant over yellow. Siliqua orientation was under digenic polymeric gene action: upright siliqua was produced by the presence of two dominant genes and spread siliqua by two recessive genes. The absence of even a single dominant gene resulted in a third type of siliqua orientation, semi‐spread siliqua.  相似文献   

3.
Five parents of common vetch (Vicia sativa L.) having orange/beige cotyledon colour, brown/white testa colour, purple/green seedling colour and purple/white flower colour were crossed as a full diallele set. The inheritance patterns of cotyledon, testa or seed coat colour, flower and seedling colour, were studied by analyzing their F1, F2, BC1 and BC2 generations. The segregation pattern in F2, BC1 and BC2, showed that cotyledon colour was governed by a single gene with incomplete dominance and it is proposed that cotyledon colour is controlled by two allelic genes, which have been designated Ct1 and Ct2. Testa colour was governed by a single gene with the brown allele dominant and the recessive allele white. This gene has been given the symbol H. Two complementary genes governed both flower and seedling colours. These flower and seedling colour genes are pleiotropic and the two genes have been given the symbols S and F.  相似文献   

4.
M. H. Rahman   《Plant Breeding》2001,120(3):197-200
The inheritance of petal (flower) colour and seed colour in Brassica rapa was investigated using two creamy‐white flowered, yellow‐seeded yellow sarson (an ecotype from Indian subcontinent) lines, two yellow‐flowered, partially yellow‐seeded Canadian cultivars and one yellow‐flowered, brown‐seeded rapid cycling accession, and their F1, F2, F3 and backcross populations. A joint segregation of these two characters was examined in the F2 population. Petal colour was found to be under monogenic control, where the yellow petal colour gene is dominant over the creamy‐white petal colour gene. The seed colour was found to be under digenic control and the yellow seed colour (due to a transparent coat) genes of yellow sarson are recessive to the brown/partially yellow seed colour genes of the Canadian B. rapa cvs.‘Candle’ and ‘Tobin’. The genes governing the petal colour and seed colour are inherited independently. A distorted segregation for petal colour was found in the backcross populations of yellow sarson × F1 crosses, but not in the reciprocal backcrosses, i.e. F1× yellow sarson. The possible reason is discussed in the light of genetic diversity of the parental genotypes.  相似文献   

5.
J. P. Singh  I. S. Singh 《Euphytica》1992,66(3):231-233
Summary Four grey mottled seed coat colour lentil lines/cultivars were crossed to one brown seed coat colour cultivar. The F1 hybrids were brown seeded in all the crosses. Segregation pattern for seed coat colour in F2 and F3 generations revealed that it is under control of a single dominant gene, which is present in the parent UPL 175 while a recessive gene is responsible for grey mottled seed coat colour in Pant L 406, Pant L 639, LG 120 and Rau 101.  相似文献   

6.
Summary Improved oil, protein and fibre contents are associated with light seed colour in rapeseed but the lack of reliable and efficient methods to measure seed colour has hindered breeding efforts for this trait. The feasibility of using light reflectance to assess seed colour in Brassica napus was examined using scanning light reflectance spectrophotometry and near infrared reflectance (NIR). Light reflectance by seed samples from 30 doubled haploid (DH) lines segregating for seed colour increased as the wavelength of the illuminating light in the scanning spectrophotometer increased between 550 and 650 nm. The largest reflectance values were measured for the yellow seed samples; the brown seed samples were intermediate and the black seed samples had the lowest reflectance values. The areas under the reflectance curves were used to transform the spectra to single values. Average light reflectance area values for the seed colour classes were significantly different from each other. The DHs and their corresponding light reflectance area values were also used to calibrate a NIR analyzer modified with 670 and 710 nm filters. The best calibration curve used three wavelengths (670, 2190 and 2208 nm) and had a multiple correlation coefficient of 0.987. Light reflectance area values determined with the calibrated NIR analyzer for 30 randomly selected breeding lines could be used to categorize the colour of the seed samples with no discrepancies between the visual and instrument classifications. The results indicate that NIR can be used to assess seed colour in rapeseed.  相似文献   

7.
B. Y. Chen  W. K. Heneen 《Euphytica》1992,59(2-3):157-163
Summary Seed colour inheritance was studied in five yellow-seeded and one black-seeded B. campestris accessions. Diallel crosses between the yellow-seeded types indicated that the four var. yellow sarson accessions of Indian origin had the same genotype for seed colour but were different from the Swedish yellow-seeded breeding line. Black seed colour was dominant over yellow. The segregation patterns for seed colour in F2 (Including reciprocals) and BC1 (backcross of F1 to the yellow-seeded parent) indicated that the black seed colour was conditioned by a single dominant gene. Seed colour was mainly controlled by the maternal genotype but influenced by the interplay between the maternal and endosperm and/or embryonic genotypes. For developing yellow-seeded B. napus genotypes, resynthesized B. napus lines containing genes for yellow seed (Chen et al., 1988) were crossed with B. napus of yellow/brown seeds, or with yellow-seeded B. carinata. Yellow-seeded F2 plants were found in the crosses that involved the B. napus breeding line. However, this yellow-seeded character did not breed true up to F4. Crosses between a yellow-seeded F3 plant and a monogenomically controlled black-seeded B. napus line of resynthesized origin revealed that the black-seeded trait in the B. alboglabra genome was possibly governed by two independently dominant genes with duplicated effect. Crossability between the resynthesized B. napus lines as female and B. carinata as male was fairly high. The sterility of the F1 plants prevented further breeding progress for developing yellow-seeded B. napus by this strategy.  相似文献   

8.
The effect of the parental genotypes and colchicine treatment on the androgenic response of wheat (Triticum aestivum L.) F1 hybrids was studied. For this, anthers from three F1 hybrids and their parents were cultured on W14 initiation medium and W14 supplemented with 0.03% colchicine. The number of responding anthers, microspore‐derived structures/100 anthers, green plants/embryos cultured, green plants/100 anthers and albino plants/100 anthers were recorded. It was observed that embryo formation and plant regeneration ability were genetically controlled and genotype dependent. In both treatments the variety Kavkaz had a significantly higher percentage of responding anthers, microspore‐derived structures and green plants/100 anthers than the other genotypes. On the other hand, the variety Myconos also demonstrated high microspore‐derived structure production and green plant regeneration when treated with colchicine. The good response observed in these two varieties indicates the importance of colchicine treatment only for certain genotypes. Green plant production capacity of the hybrids was intermediate to that of the parental varieties. As one parent with a high or even an intermediate response to anther culture could lead to the production of sufficient (for breeding purposes) green plants from the F1 hybrids, it was concluded that screening the inbred lines for the response to anther culture with and without colchicine treatment could contribute to utilization of breeding material with a low response to anther culture via the proper hybrid combinations.  相似文献   

9.
Summary Barley breeders at ICARDA have observed that genotypes adapted to dry regions have leaves which are lighter in colour than those of unadapted ones. We measured photosynthesis, chlorophyll content and chlorophyll a:b ratios in two sets of genotypes which had previously been observed to have either light green or dark green leaves when grown in the field. Thylakoid membranes were also extracted and the proteins analysed on SDS-PAGE gels.The light leaf colour was associated with a higher chlorophyll a:b ratio. This was a measure of a reduction in the amount of antenna chlorophyll compared to that in the core complex of PSII. Genotypes with light green leaves had consistently less chlorophyll per unit leaf area and lower photosynthetic rates per unit area than those with dark green leaves.It is suggested that these features of light green leaves may confer the ability to adapt to high levels of irradiance under drought conditions. This ability may result from a high rate of photosynthetic electron transport through each PSII reaction centre, thus reducing the risk of damage from the overexcitation of these centres.  相似文献   

10.
The inheritance of siliqua locule number and seed coat colour in Brassica juncea was investigated, using three lines each of tetralocular brown seeded and bilocular yellow seeded. Three crosses of tetralocular brown seeded × bilocular yellow seeded lines were attempted and their F1, F2 and backcross generations were examined for segregation of these two traits. Brown seed colour and bilocular siliqua characters were found to be dominant over yellow seed and tetralocular siliqua, respectively. Chi‐square tests indicated that each trait is controlled by different sets of duplicate pairs of genes. Bilocular siliquae or brown seeds can result from the presence of either of two dominant alleles, whereas tetralocular siliquae or yellow seeds are produced when alleles at both loci are recessive. A joint segregation analysis of F2 data indicated that the genes governing siliqua locule number and seed colour were inherited independently.  相似文献   

11.
Anthocyanidins were identified in 28 Dendrobium species and hybrids selected for analysis based on colour and suitability in cut flower breeding. Flowers designated pink, red, maroon, orange, bronze, and brown in the trade were placed in RHS colour groups red-purple, purple-violet, violet on yellow, greyed-purple on yellow or yellow-orange, and brown. This colour range contained anthocyanins based on cyanidin, with peonidin occurring as a minor pigment. The colours of three blue genotypes, D. gouldii K280-6, D. biggibum ‘blue’, and D. Kultana ‘blue’, were light violet to purple by RHS standards and contained anthocyanins based on cyanidin. Peach-coloured flowers were classified as red or red-purple and included pelargonidin glycosides. Anthocyanin concentrations ranged from 0.13 to 0.18 μmoles/g FW in light lavender and peach, and up to 3.66 μmoles/g FW in brown. Combined cellular and vacuolar pH ranged narrowly from 4.67 to 5.09 among white, peach, lavender, and brown lines. Predominant copigments were flavonol glycosides based on kaempferol, quercetin, myricetin, and methylated derivatives. Flavonol aglycones and glycosylation sites differed little among two colour forms of D. gouldii and two D. Jaquelyn Thomas hybrids. Accumulation of quercetin, myricetin, and cyanidin indicated flavonoid 3' and 3',5' hydroxylation activities in several Dendrobium. Additional accumulation of isorhamnetin, syringetin, and peonidin indicated active flavonoid 3'- and 3',5'- O-methyltransferase enzymes. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

12.
Colour is one of the most important quality attributes of broccoli. Yellowing due to senescence of broccoli florets is the main external quality problem. Controlled atmosphere (CA) storage is a very effective method to maintain broccoli quality. The aim of this paper is to characterise the colour behaviour (measured by RGB colour image analysis) of broccoli as affected by CA and temperature. Data on colour behaviour and gas exchange were gathered for broccoli heads stored in containers at three temperatures and subjected to four levels of O2 and three levels of CO2 concentrations. An integrated colour model is proposed that combines a colour model with a standard gas exchange model. The colour model is based on an existing colour model that describes the formation of (blue/green) chlorophyllide from the colourless precursor, the bidirectional conversion of chlorophyllide into (blue/green) chlorophyll and the decay of chlorophyllide. A multi-response approach was applied, accounting for 92% of the variance. Gas exchange parameters were estimated using the gas exchange model, the colour parameters were estimated using the colour model. Both models are linked via the reaction rate constant that describes the decay of chlorophyllide, as this reaction rate constant was found to be affected by the gas conditions. The integrated model might be applied to predict colour changes of MAP packaged broccoli as a low level of O2 and a high level of CO2 will only affect colour retention at higher temperatures.  相似文献   

13.
B. Sharma  M.K. Emami 《Euphytica》2002,124(3):349-353
A new gene is reported which functions as a master gene for synthesis of the pigments determining cotyledon colour in lentil. This gene is different from the two earlier reported genes which are responsible for synthesis of yellow (gene Y) and brown (gene B) pigments. Double recessive homozygous condition of these two genes results into loss of both pigments and, consequently, produces light green cotyledons. The new gene, in contrast, produces dark green cotyledons in recessive condition irrespective of the dominance or recessive state of the Y and B genes. It is hypothesized that the new gene for dark green cotyledon colour (Dg) acts at an earlier stage in the biosynthesis of the two cotyledon-specific pigments, which are derived from a common precursor, whose synthesis is blocked when Dg mutates to its recessive condition. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

14.
J. R. Baggett 《Euphytica》1978,27(2):593-599
Summary Internal anthocyanin pigmentation (IP) in otherwise normally green cabbage occurs in a number of Oregon State University breeding lines. Extracted pigment, tested for spectral absorption and for color reactions with lead acetate and aluminium chloride, was similar but not necessarily identical to pigment extracted from red cabbage cultivar Redman. When IP line R52 was crossed with normal green line C70, the F1, F2 and backcross progenies indicated that IP at the intensity found in R52 was determined by a single factor in homozygous condition, with intermediate levels of IP expressed by the heterozygous genotypes. Modifying factors also appear to influence the level of IP. In the cross R52 (IP)×R51 (normal green), expression of IP in the F1 was much reduced. The F2 failed to fit the expected 3 IP: 1 green ratio due to an excess of green plants, but instead, closely fit a 9:7 ratio. This may have resulted from incomplete expression of IP because of modifiers, rather than from the effects of a second major gene. An allele at the A (anthocyanin) locus of B. oleracea is tentatively proposed and designated A IP or a IP pending further identification.Oregon Agricultural Experiment Station Technical Paper No. 4690.  相似文献   

15.
Production of yellow-seeded Brassica napus through interspecific crosses   总被引：12，自引：0，他引：12  
M. H. Rahman   《Plant Breeding》2001,120(6):463-472
Yellow‐seeded Brassica napus was developed from interspecific crosses between yellow‐seeded Brassica rapa var.‘yellow sarson’ (AA), black‐seeded Brassica alboglabra (CC), yellow‐seeded Brassica carinata (Bbcc) and black‐seeded B. napus (AACC). Three different interspecific crossing approaches were undertaken. Approaches 1 and 2 were designed directly to develop yellow‐seeded B. napus while approach 3 was designed to produce a yellow‐seeded CC genome species. Approaches 1 and 2 differed in the steps taken after trigenomic interspecific hybrids (ABC) were generated from B. carinata×B. rapa crosses. The aim of approach 1 was to transfer the yellow seed colour genes from the A to the C genome as an intermediate step in developing yellow‐seeded B. napus. For this purpose, the ABC hybrids were crossed with black‐seeded B. napus and the three‐way interspecific hybrids were self‐pollinated for a number of generations. The F7 generation resulted in the yellowish‐brown‐seeded B. napus line, No. 06. Crossing this line with the B. napus line No. 01, resynthesized from a black‐seeded B. alboglabra x B. rapa var.‘yellow sarson’ cross (containing the yellow seed colour genes in its AA genome), yielded yellow‐seeded B. napus. This result indicated that the yellow seed colour genes were transferred from the A to the C genome in the yellowish‐brown seed colour line No. 06. In approach 2, trigenomic diploids (AABBCC) were generated from the above‐mentioned trigenomic haploids (ABC). The seed colour of the trigenomic diploid was brown, in contrast to the yellow seed colour of the parental species. Trigenomic diploids were crossed with the resynthesized B. napus line No. 01 to eliminate the B genome chromosomes, and to develop yellow‐seeded B. napus with the AA genome of ‘yellow sarson’ and the CC genome of B. carinata with yellow seed colour genes. This interspecific cross failed to generate any yellow‐seeded B. napus. Approach 3 was to develop yellow‐seeded CC genome species from B. alboglabra×B. carinata crosses. It was possible to obtain a yellowish‐brown seeded B. alboglabra, but crossing this B. alboglabra with B. rapa var.‘yellow sarson’ failed to produce yellow seed in the resynthesized B. napus. The results of approaches 2 and 3 demonstrated that yellow‐seeded B. napus cannot be developed by combining the yellow seed colour genes of the CC genome of yellow‐seeded B. carinata and the AA genome of ‘yellow sarson’.  相似文献   

16.
Summary Seedcoat colour in greengram (Vigna radiata (L.) Wilczek.) is a useful marker for genetic studies and varietal identification. Its mode of inheritance was examined in five crosses among nine parents which differed for seedcoat colour. Four of the parents had sap green seedcoat colour while the others had raw sienna, brownish green, densely black spotted, black and greenish yellow seedcoat colour, respectively. At the F2 generation, no more than 20 different colour classes were observed. The segregation in F3 and backcross generations indicated that at least five major genes were involved in seedcoat colour inheritance. Sap green seemed to be dominant over raw sienna. The segregation ratios further indicated the role of non-allelic gene interactions (epistasis) in inheritance of seedcoat colour. Gene symbols were assigned to each colour and genotypes to each parent.  相似文献   

17.
One thousand four hundred and seven spring wheat germplasm lines belonging to Indian and CIMMYT wheat programs were evaluated for stay green (SG) trait and resistance to spot blotch caused by Bipolaris sorokiniana during three consecutive crop seasons, 1999–2000, 2000–2001 and 2001–2002. Disease severity was recorded at six different growth stages beginning from tillering to late milk stage. SG trait was measured by following two approaches: difference for 0–9 scoring of green coloration (chlorophyll) of flag leaf and spike at the late dough stage (GS 87) and a new approach of leaf area under greenness (LAUG). Germplasm lines showed a wide range (7–89) for LAUG and were grouped into four viz., SG, moderately stay green, moderately non-stay green and non-stay green (NSG). However, very few (2.2%) lines showed high expression of SG trait, i.e., LAUG >60. LAUG appeared to be a better measure of SG trait than a 0–9 scale. Mean spot blotch ratings of SG genotypes were significantly lower than those of NSG genotypes at all growth stages. Two spot blotch resistant genotypes (Chirya 3 and Chirya 7) having strong expressions of SG trait were crossed with NSG, spot blotch susceptible cv. Sonalika. Individually threshed F2 plants were used to advance the generations. SG trait and spot blotch severity were recorded in the parents and F1, F3, F4, F5, F6 and F6–7 generations under disease-protected and inoculated conditions. SG trait in the F1 generation was intermediate and showed absence of dominance. Evaluation of progenies (202–207) in the segregating generations revealed that SG trait was under the control of around four additive genes. Lines homozygous for SG trait in F4, F5, F6 and F6–7 generations showed significantly lower mean area under disease progress curve (AUDPC) for spot blotch than those with NSG expression. A positive correlation (0.73) between SG trait and AUDPC further indicated a positive influence of SG on severity of spot blotch. The study established that variation for SG trait exists in spring wheat; around four additive genes control its inheritance in the crosses studied and there is positive association between SG trait and resistance to spot blotch.  相似文献   

18.
Summary Ethiopian landraces of tetraploid wheat can be grouped according to their seed colors in three major groups: brown, purple and white seeded. Seeds with different colours are used for different purposes, and the three seed colour groups are treated separately in breeding programs. The genetic variation between and within these groups was studied by isozyme analyses at six highly polymorphic loci in sixty landrace agrotypes. The mean number of alleles per locus was 1.95. The mean allele frequencies showed significant variation both within and between the seed colour groups. The brown and white seeded types had very high genetic identity and the genetic identity values between the brown and purple and the purple and white groups were only slightly smaller. The average coefficient of gene differentiation between the seed colour types was very low. Only about 5% of the total genetic variation was due to differences between the seed colour groups. This indicates that agrotypes of different seed colours can not be treated as genetically separate and distinct groups.  相似文献   

19.
Y. Dutt    X. D. Wang    Y. G. Zhu  Y. Y. Li 《Plant Breeding》2004,123(2):145-151
In the present study, three types of coloured fibre cottons, i.e. white, brown and green, were compared for their fibre quality and yield. The comparison of fibre quality suggested that coloured fibre cotton was inferior as compared with white fibre cotton. To understand the effect of cellulose, mineral elements [nitrogen (N), phosphorus (P) and potassium (K)] and pH of fibre cells on the quality of fibre, these components were studied at different fibre cell developed stages in all three fibre cotton types. The cellulose content is closely associated with the quality of fibre. The higher fibre quality of white fibre cotton might be the result of the high cellulose content in it compared with coloured fibre cotton. A rapid and slow decrease in pH in white and coloured cottons, respectively, might have some effects on fibre elongation. Among the mineral contents, potassium is positively correlated with the fibre quality traits. The pigment development patterns in brown and green fibre cottons are not similar. In green fibre cotton it takes more time to deepen in colour as compared with brown fibre cotton. Possible strategies for the improvement in quality of coloured fibre cotton are discussed. The results of heterosis studies in coloured fibre cotton suggest that heterosis could improve yield and quality of coloured fibre cotton. In the present study, the hybrids between ZJU12A x ZJU05R and ZJU18A x ZJU01R, having an acceptable lint colour types plus better fibre quality and high yield performance, may be exploited further for their heterotic advantages.  相似文献   

20.
The colour of mangosteen (Garcinia mangostana L.) fruit changes from green to purple black after harvest as the fruit ripens, and is used as a quality guide for growers and consumers. We determined the relationship between anthocyanin composition and content during fruit colour development in relation to fruit maturity and postharvest quality. Fruit at different stages of maturity (light greenish yellow with 5% scattered pink spots to purple black) were harvested and kept at 25 °C (85–90% RH). Fruit from each maturity stage all developed to the final purple black stage. During the postharvest period, hue angle values and pericarp firmness decreased significantly, while soluble solids contents increased. Anthocyanin contents in the outer pericarp were higher than in the inner pericarp and increased to a maximum at the final colour stage. Sensory evaluation and fruit quality (hue angle values, soluble solids and titratable acidity) of fruit harvested at the different stages did not differ once the fruit had finally developed to the purple black stage. The anthocyanins in the outer pericarp mainly consisted of five compounds, identified by HPLC/MS as cyanidin-sophoroside, cyanidin-glucoside, cyanidin-glucoside-pentoside, cyanidin-glucoside-X, cyanidin-X2 and cyanidin-X, where X denotes an unidentified residue of m/z 190, a mass which does not correspond to any common sugar residue. Cyanidin-3-sophoroside and cyanidin-3-glucoside were the major compounds and the only ones that increased with fruit colour development.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号