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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
21

Identification of cytoskeletal proteins as substrates for Ca'2'+ dependent protein kinase

Ritchie, Sian January 1994 (has links)
No description available.
22

Nutrient recycling and sourcing by Faidherbia albida trees in Malawi

Phombeya, Henry Stevie Kondwani January 1999 (has links)
No description available.
23

Ambient drying of maize

Some, D. K. A. January 1985 (has links)
No description available.
24

The molecular analysis of A1-homologous and C1-homologous clones from ubiquitous lines of maize

Spencer, Richard Anthony January 1990 (has links)
No description available.
25

The isolation of a transposable element inserted in an A1 (anthocyanin-1) allele of Zea mays

Franklin, Tanya Michelle January 1990 (has links)
No description available.
26

Delia : a gene regulating pigmentation pattern in Antirrhinum majus

Goodrich, Justin January 1992 (has links)
No description available.
27

Genetic manipulation of Zea mays L

Southgate, Elizabeth M. January 1996 (has links)
No description available.
28

Species selection for alley cropping in Western Kenya : system management, nutrient use efficiency and tree-crop compatibility (1988-1995)

Heineman, Arne M. January 1996 (has links)
No description available.
29

Evaluation of Argentine maize hybrids and exotic x temperate testcrosses across environments

Ochs, Brett Allen 01 November 2005 (has links)
Maize (Zea mays L.) is grown in a wide range of environments and altitudes worldwide. Maize has transitioned from open pollinated varieties to single cross hybrids over the last century. While maize production and genetic gain has increased, genetic diversity among U.S. maize hybrids has narrowed. Problems, such as insect pressure, diseases, and mycotoxins, present obstacles for breeders. One approach is to use exotic germplasm in breeding programs to provide useful, novel alleles for productivity, grain quality, and disease resistance. Little exotic germplasm has been used, because of lack of agronomic adaptation and problems with lodging, earliness, and tall plants in more temperate areas. Using exotic elite materials and evaluating them in targeted regions might increase success. Objectives of this research were: to characterize and evaluate agronomic adaptation and performance of Argentine commercial hybrids in the U.S., to evaluate semi-exotic testcrosses developed from semi adapted 100% tropical lines and elite U.S. inbred LH195, and to estimate response to aflatoxin contamination of Argentine hybrids and semi-exotic testcrosses under inoculation with Aspergillus flavus. Agronomic data was collected during 2004 in eleven Texas environments for Argentine hybrids, and eight Texas environments for semi-exotic testcrosses. Response to aflatoxin was measured in three southern Texas environments. U.S. commercial hybrids were used as checks. Significant differences among hybrids were observed for most environments and traits. In general, Argentine hybrids yielded lower, had lower 1000 kernel weights, and greater test weights than U.S. hybrids. Hybrids AX889, AX882MG, and AX890MG were competitive with U.S. hybrids for grain yield and were stable across environments. Semi-exotic testcrosses had similar lodging and grain moisture percentages, heavier test weights and competitive grain yields compared with U.S. hybrids. Hybrid TX-LAMA2002-9-2-B/lH195 had the highest overall grain yield mean for semi-exotic testcrosses and yielded better than two U.S. hybrids. Argentine hybrids had lower aflatoxin concentration than U.S. hybrids; several hybrids had less than 50 ng g-1 aflatoxin. Semi-exotic testcrosses had reduced aflatoxin compared to U.S. hybrids, with several hybrids under 35 ng g-1. These elite, exotic materials show promise for breeding programs, with competitiveness for grain yield, kernel traits, and reduced aflatoxin levels.
30

Genetic diversity and performance of maize varieties from Zimbabwe, Zambia and Malawi

Magorokosho, Cosmos 25 April 2007 (has links)
Large scale and planned introduction of maize (Zea mays) in southern Africa was accomplished during the last 100 years. Since then, smallholder farmers and breeders have been selecting varieties best adapted to their specific growing conditions. Six studies were conducted to generate information on the current levels of genetic diversity and agronomic performance of both farmer-developed and commercially-bred maize varieties in Zimbabwe, Zambia and Malawi to help in the identification of sources of new alleles for improving yield, especially under the main abiotic stresses that prevail in the region. In the first study, 267 maize landraces were collected from smallholder farmers in different agro-ecological zones of the three countries for conservation and further studies. Passport data and information on why smallholder farmers continue to grow landraces despite the advent of modern varieties were also collected along with the landraces. The second study revealed considerable variation for phenological, morphological and agronomic characters, and inter-relationships among the landraces and their commercial counterparts. A core sample representing most of the diversity in the whole collection of landraces was selected for further detailed analyses. The third study revealed high levels of molecular diversity between landraces originating from different growing environments and between landraces and commercially-bred varieties. The Simple Sequence Repeat (SSR) data also showed that the genetic diversity introduced from the original gene pool from the USA about 100 years ago is still found in both the descendant landraces and commercially-bred varieties. The fourth study showed that in general, commercially-bred varieties outyielded landraces under both abiotic stress and nonstress conditions with some notable exceptions. Landraces were more stable across environments than improved varieties. The most promising landraces for pre-breeding and further investigation were also identified. The clustering patterns formed based on agronomic data were different from SSR markers, but in general the genotype groupings were consistent across the two methods of measuring diversity. In the fifth study, the more recently-bred maize varieties in Zimbabwe showed consistent improvement over older cultivars in grain yield. The apparent yearly rate of yield increase due to genetic improvement was positive under optimum growing conditions, low soil nitrogen levels and drought stress. The sixth study revealed that in general, genetic diversity in Zimbabwean maize has neither significantly decreased nor increased over time, and that the temporal changes observed in this study were more qualitative than quantitative. The results from the six studies confirm the origin of maize in southern Africa and reveals that considerable genetic variation exists in the region which could be used to broaden the sources of diversity for maize improvement under the current agro-ecological conditions in southern Africa.

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