Effects of Time and Rate of Nitrogen and Phosphorus Application on the Growth and the Seed and Oil Yields of Canola (Brassica napus L.)

A field study was conducted to investigate the influence of variable rates of application of N and P fertilizers in splits at various times on the growth and the seed and oil yields of canola (Brassica napus L.) during 1995–97. Rates of fertilizer application were 0 and 0 (F0), 60 and 0 (F1), 0 and 30 (F2), 60 and 30 (F3), 90 and 60 (F4) and 120 and 90 (F5) kg N ha^?1 and kg P₂O₅ ha^?1. All the P was applied at sowing while N was applied in splits, i.e. all at sowing, half at sowing and half with first irrigation, or half at sowing and half at flowering. The responses of growth, seed yield and components of yield were consistent in both years. Increasing the rate of fertilizer application from F4 (90/60 kg N/P₂O₅ ha^?1) to F5 (120/90 kg N/P₂O₅ ha^?1) increased the leaf area index (LAI) relative to the control and to lower rates of fertilizer application. For both crops, application of 90/60 kg N/P₂O₅ ha^?1 significantly enhanced total dry matter (TDM) and seed yield. Seed yield increased mainly due to a greater number of pods per plant and seeds per seed‐pod. The time of fertilizer application did not significantly affect seed yield or components of yield in either season. Oil yield generally followed seed yield, increasing with increasing rate of fertilizer application up to 90/60 kg N/P₂O₅ ha^?1. The maximum oil contents were obtained from the control. The results show that seed and oil yields of canola were maximized at the F4 (90/60 kg N/P₂O₅ ha^?1) rate of application under the agro‐ecological conditions of Faisalabad, Pakistan.     

Identification of cultivars of pasture legumes (Centrosema macrocarpum,C. pubescens and C. sp.n.) by acid polyacrylamide gel electrophoresis of cotyledons storage proteins

Summary An electrophoretic procedure was developed for storage proteins which can discriminate cultivars of forage legumes, Centrosema macrocarpum, C. pubescens and C. sp.n. Proteins extracted from cotyledons were separated in 10% polyacrylamide gel containing 10% sucrose. Electrophoretic patterns are presented to illustrate the results that can be obtained with the procedure described. Cultivars of all three species were distinguishable based upon the variation in their acid soluble seed proteins.Joint publiccation of the Department of Food Science, University of Manitoba (No 101) and Centro Internacional de Agricultura Tropical-CIAT.     

Isoenzyme and cotyledon protein variation for identification of black beans (Phaseolus vulgaris L.) with similar seed morphology

Summary Methods developed to identify genetically diverse varieties of beans (Phaseolus vulgaris L.) were applied to closely related lines that were difficult to distinguish on the basis of seed morphology. Seedling tissues and seeds of black beans, were examined electrophoretically for isoenzyme and cotyledon proteinn protein patterns. Seven enzymes, extracted from seeds or from seedling stem, root or leaf tissues, were compared for polymorphism. Peptidase, polyphenol oxidase, phosphoglucoisomerase and glutamate oxaloacetate transaminase patterns were the same for all lines. Some differences were observed for acid phosphatase, peroxidase and esterase patterns, but complete discrimination of the six selected lines was not possible on the basis of isoenzyme patterns alone. Using polyacrylamide gel electrophoresis (PAGE) of dissociated 0.1 M acetic acid soluble proteins at pH 3.1 (acid-PAGE), or sodium dodecyl sulphate PAGE (SDS-PAGE) of residual protein extracts, all but one pair of samples in each case could be distinguished from the other samples. Using both techniques all of the lines could be identified unequivocally.     

Selection of diverse parents of chickpea (Cicer arietinum L.) by multivariate analysis and the degree of heterosis of their F1 hybrids

Summary Studies on genetic diversity in chickpea (Cicer arietinum L.) indicated the existence of considerable amount of variation for grain yield and its components in the material. One hundred and thirty two genotypes fell into eight clusters. The covariation structure studied by means of factor analysis indicated the possibility of obtaining, through hybridization, genotypes physiologically and morphologically more efficient. Multivariate analysis of data from 7 parents and 21 F1 hybrids indicated weak correspondence between D²-analysis and canonical variate analysis. As there was no relationship between heterosis over midparent and genetic distance between the parents, so the traditional approach of making a large number of crosses is being suggested.     

Rhizobium specificity of Trifolium ambiguum M. Bieb × T. repens L. hybrid clovers

Growth of full-sib families of an F₁ interspecific hybrid between Trifolium ambiguum M.Bieb and T. repens L, and two generations of backcross hybrids (BC₁F₂ and BC₂F₁) with T. repens as the recurrent parent, were compared to their parental species. Plants were grown in a N-free medium and inoculated with Rhizobium leguminosarum biovar trifolii rhizobia effective on T. ambiguum or T. repens. Hybridisation produced progeny that nodulated with rhizobia from either T. ambiguum or T. repens, but plant growth varied. Mean weights of T. repens and hybrids, particularly F₁ and BC₁F₂, were higher when inoculated with a mixture of strains isolated from field grown T. repens than with the New Zealand inoculant strain for T. repens. When inoculated with the mix of rhizobia from T. repens, mean weights were 242, 189, 132, 125, and 100 mg/plant for T. repens, BC₂F₁, BC₁F₂, F₁ and T. ambiguum, respectively. However, although the mean weight of BC₂F₁ lines was significantly less than T. repens, there was considerable variation in individual full-sib families indicating the potential to select within BC₂F₁ hybrids for high plant growth/symbiotic nitrogen fixation. The weight of T. ambiguumplants inoculated with the New Zealand inoculant strain for hexaploid T. ambiguum was similar to T. repens inoculated with the mix of rhizobia from T. repens (253 and 242 mg/plant, respectively). Mean fresh weights of F₁ hybrid plants were similar when inoculated with rhizobia for T. ambiguum or T. repens (125 and 130 mg/plant, respectively). However, weight of T. repens, BC₁F₂ and BC₂F₁ hybrids inoculated with rhizobia for T. ambiguum were all less than 90 mg/plant. There was a significant relationship between plant fresh weight and ethylene production. The results indicate that measuring weights of inoculated plants growing in N-free media is a rapid initial method of screening a range of plant germplasm for plant growth/symbiotic nitrogen fixation rates. This revised version was published online in August 2006 with corrections to the Cover Date.     

Detection of molecular markers linked to the durable adult plant stripe rust resistance gene Yr18 in bread wheat (Triticum aestivum L.)

Stripe rust of wheat caused by Puccinia striiformis West. f. sp. tritici presents a serious problem for wheat production worldwide, and identification and deployment of resistance sources to it are key objectives for many wheat breeders. Here we report the detection of simple sequence repeat (SSR) markers linked to the durable adult plant resistance of cv. ‘Otane’, which has conferred this resistance since its release in New Zealand in 1984. A double haploid population from a cross between ‘Otane’ and the susceptible cv. Tiritea’ was visually assessed for adult plant infection types (IT) in the glasshouse and field, and for final disease severity in the field against stripe rust pathotype 106E139A⁺. At least three resistance loci controlled adult plant resistance to stripe rust in this population. Quantitative trait loci (QTL) mapping results revealed that two of these, one on chromosome 7DS corresponds to the durable adult plant resistance gene Yr18 and other on chromosome 5DL were contributed from ‘Otane’; while the remaining one on chromosome 7BL, was contributed from the susceptible ‘Tiritea’. Interval mapping placed the ‘Otane’‐resistant segment near the centromere of chromosome 7DS at a distance of 7 cM from the SSR marker gwm44. The stability of QTL in the two environments is discussed. SSR gwm44 is potentially a candidate marker for identifying the durable resistance gene Yr18 in breeding programmes.     

Effect of Changing Temperature on the Deterioration of Soya Beans

Deterioration rates as indicated by carbon dioxide evolution for soya bean (Glycine max L. Merr.) stored under changing temperature conditions were quantified and compared with those predicted using equations. Experiments included soya bean moisture contents of 18, 22, and 26% (wet basis), constant storage temperatures of 15, 20, 25, and 30°C, and cyclical storage temperatures that changed between 15 and 25°C and between 20 and 30°C on a 24 h basis. Also, the growth of micro-organisms was identified after 10 days from the treatments by using the pour plate method.The results indicated an increase in deterioration by increasing storage temperature and moisture content of soya bean. Equations of carbon dioxide weight versus time for each moisture content and storage temperature were fitted. The longest allowable storage time to reach 0·5% dry matter loss (1132 h) occurred at lower moisture content and lower constant storage temperature, while the shortest allowable storage time (170 h) occurred at higher moisture content and higher constant storage temperature. The allowable storage times for soya bean stored under cyclical temperatures were close to the allowable storage time for soya bean stored at a constant temperature equal to the average cyclical temperature. Microbial infection levels increased with increasing storage temperature and moisture content. The increasing rate of micro-organism growth decreased by increasing the storage temperature over 25°C. However, this increasing rate of micro-organism growth for soya bean exposed to a cyclical storage temperature was usually lower than that for soya bean held at constant storage temperatures of about 20°C (the average of 15 and 25°C) and 25°C (the average of 20 and 30°C).     

Time-resolved X-ray diffraction studies of the B in equilibrium D structural transition in the DNA double helix

Because of the relation between topology and function, there has been much interest in the structural transitions of the various conformations of DNA polymers. The x-ray fiber diffraction analysis system at the Daresbury Synchrotron Radiation Source was used to study the reversible transition between the B and D forms of the synthetic DNA poly[d(A-T)].poly[d(A-T)]. The gradual progression of conformations between these two forms indicates that the DNA double helix does not undergo a change of handedness during this transition.