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首页> 外文期刊>International journal of agricultural research >Establishment of Distinct Core Collections based on the Predicted Genotypic Value of Ethiopian Fenugreek ( Trigonella foenum-graecum L.) Landraces
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Establishment of Distinct Core Collections based on the Predicted Genotypic Value of Ethiopian Fenugreek ( Trigonella foenum-graecum L.) Landraces

机译:基于预测的埃塞俄比亚胡芦巴(Trigonella foenum-graecum L.)地方品种基因型价值的独特核心集合的建立

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In order to evaluate selection procedures 144 random sample of fenugreek accessions collected from locations at heights ranging from 1750 to 3150 m, along with one released variety, were used in this study for designating a core collection representative of the whole range of accessions used in the study. The field experiment was conducted at Adadi and Ambo Research Center during 2006 and 2007 main cropping seasons. Treatments were arranged in a 12x12 simple lattice design. The data were subjected to multivariate analyses for different clustering methods, performed using the SAS software. Homogeneity test (F-test) for variance and a t-test for means (0.05) were performed to determine the differences of traits between the core and the initial collections. Furthermore, the characteristic of the core collection in terms of the initial collection was determined by coincidence rate and the variable rate. Core collections established by distinct clustering and sampling methods were representatives of the initial collection, with exception of the collection constructed by Wards clustering method combined with random sampling. This observation indicates that the genetic variation available in the initial collection can be preserved in the nine established core collections. These core subsets can be used as a point of entry for efficient and effective exploitation of germplasm resources for the improvement of the crop.
机译:为了评估选择程序,在本研究中使用144个从1750至3150 m高度的位置收集的胡芦巴种质的随机样品,以及一种已发布的品种,来指定代表该种使用的所有种质的核心种质。研究。在2006年和2007年主要农作物季节期间,在Adadi和Ambo研究中心进行了田间试验。处理安排为12x12的简单格子设计。使用SAS软件对数据进行了不同聚类方法的多元分析。进行方差的均一性检验(F检验)和均值的t检验(0.05),以确定核心和初始集合之间性状的差异。此外,核心集合在初始集合方面的特征由重合率和可变率确定。通过独特的聚类和采样方法建立的核心集合是初始集合的代表,但通过Wards聚类方法结合随机采样构建的集合除外。该观察结果表明,初始收集物中可用的遗传变异可以保留在九个已建立的核心收集物中。这些核心子集可以用作有效利用种质资源改善作物的切入点。

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