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Meat quality of fattening pigs fed yellow lupin-based diets. The 30 crossbred pigs [(Landrace x Yorkshire) x Duroc] were fattened in 3. phase fattening period. In their nutrition as a source of protein was used soybean meal (Group C) or soybean meal and seeds of yellow lupine in the amount of 7.5% (Group E1) and 15% (Group E2). After achieving body weight of about 117.5 kg animals were slaughtered. The samples of Musculus longissimus lumborum collected from all slaughtered pigs. Significant differences were found in drip loss percentage between groups C and E1 (P ≤0.05). As regards the fatty acids, there were lower proportions of C18:2 in group E1 vs C (P ≤0.05) and of C18:2 and C20:4 in group E2 vs C (P ≤0.01). Differences in PUFA percentage, PUFA/SFA ratio, and proportion of n-6 fatty acids were significant, with lower values of the traits in group E1 vs C (P ≤0.05) and in group E2 vs C (P ≤0.01), which shows that the dietetic value of pork has slightly deteriorated. The chemical composition and the physical parameters of the meat samples were normal and at a similar level in all the groups.
The paper presents an analysis of the impact of meteorological factors (solar radiation, maximum, minimum and mean temperature, precipitation) on the development and yield of yellow lupin Parys cultivar in the northern Poland in the years 1987–2008. Using multiple regression methods (linear and quadratic function) created regression equations that were estimated using the coeffi cients of determination (R2, R2 adj and R2 pred – using the Cross Validation procedure). Selected regression equation used to estimate the yield of yellow lupin, using generated – by means of model WGENK – daily values of global radiation, maximum and minimum temperature, precipitation, and climate change scenario GISS Model E for Central Europe. Examined dependencies weather-yield of lupine seeds (cultivar Parys) allowed the application of the chosen model to forecast yields from the time when the values are independent variables in the model by the end of the growing season. The comparison of distributions of actual and simulated yields shows that real yields are slightly (by 0.06 t·ha–1) higher than those generated for 2 × CO2 conditions.
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Enzymatic activity of nickel-contaminated soil

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A pot experiment was performed to determine the effect of soil contamination with nickel, applied at a dose of 100, 200, 300 and 400 mg kg-1, on the activity of dehydrogenases, urease, acid phosphatase and alkaline phosphatase. The impact of nickel on the enzymatic activity of soil was studied on samples of heavy loamy sand and light silty loam. The experiment was conducted in two series: in the first one soil was cropped to yellow lupine, and in the second one it was left uncropped. Soil samples were analyzed on day 14, 28, 42 and 56. It was found that soil contamination with nickel reduced the activity of all the enzymes. This negative influence was most noticeable in the case of dehydrogenase. The activity of urease and alkaline phosphatase was higher in light silty loam, while the activity of dehydrogenases and acid phosphatase was higher in heavy loamy sand. The activity of dehydrogenases and urease was higher in soil cropped to yellow lupine, whereas the activity of acid phosphatase and alkaline phosphatase was higher in uncropped soil. Yellow lupine was sensitive to excessive amounts of nickel in the soil, and partly alleviated the adverse impact of this heavy metal on urease activity, but did not reduce its inhibitory effect on the other enzymes.
A strict two-factor field experiment was set up as a randomized complete block design over 2000-2002 at the Experimental Station of the Faculty of Agriculture, University of Technology and Agriculture, at Mochełek, and involved a traditional yellow lupin cultivar, `Idol´, whose plants were sprayed with Tytanit preparation, containing 46% of Ti. The first factor covered the following objects: three spraying dates: single spraying after blossom fall, double spraying - after blossom fall and 7-10 days later and triple spraying - after blossom fall, 7-10 days later and then 7-10 days later. The second factor involved the following objects of Tytanit concentration: 0.02, 0.04 and 0.06%. The plots which were not sprayed constituted the control. Throughout the research years there was observed a significant effect of Tytanit on 7.4-18% increased yellow lupin seed yield. Tytanit did not show a significant effect on the structural components of the seed yield from the main stem; its application resulted in a significant, as compared with the control, increase in the number of pods and seeds as well as in the seed weight from branches. As for yellow lupin yielding, the optimal solution seems to be offered by a double application of 0.02-0.04% of Tytanit straight after plant blossom fall and 7-10 days later.
The research aimed at defining the variability in the yielding of yellow lupin cultivated in pure stand and in mixtures with spring triticale in a field experiment at a varied April-July rainfall as well as a varied sowing density of both components. The experiments were carried out over 1990-1993 at the Mochełek Experiment Station of the Bydgoszcz University of Technology and Agriculture, Faculty of Agriculture. The experiments were conducted on light soil of a good rye soil suitability complex, IVa soil quality classification. The value of the rainfall variability coefficient over April-July amounted to 37.1%. The driest period rainfall amounted to 106 mm, while the most moisten period rainfall - 260 mm. It was observed that the yellow lupin yielding variability in pure stand was considerably lower than in the mixtures with spring triticale. An increasing lupin sowing density from 25 to 50-100 seeds per 1 m2, both in pure stand and in mixtures, showed a stabilising effect on the seed yield and pl.
Two full copy cDNA sequences encoding chalcone synthase (CHS) were selected from a yellow lupin (Lupinus luteus L.) root and nodule cDNA library, and sequenced. Analysis of their open reading frames gave evidence that both encode the functional enzyme. Sequence alignment and phylogenetic studies on the DNA and protein level of these clones compared to the sequences of chalcone synthases from 54 other plant species reveal the possibility that lupin chalcone synthase is encoded by a multigene family consisting of at least two distinct genes that probably diverged by gene duplication. The duplication event is estimated to have taken place about 16 million years ago.
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