Spelling suggestions: "subject:"maize"" "subject:"daize""
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Identification of cytoskeletal proteins as substrates for Ca'2'+ dependent protein kinaseRitchie, Sian January 1994 (has links)
No description available.
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Nutrient recycling and sourcing by Faidherbia albida trees in MalawiPhombeya, Henry Stevie Kondwani January 1999 (has links)
No description available.
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Ambient drying of maizeSome, D. K. A. January 1985 (has links)
No description available.
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The molecular analysis of A1-homologous and C1-homologous clones from ubiquitous lines of maizeSpencer, Richard Anthony January 1990 (has links)
No description available.
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The isolation of a transposable element inserted in an A1 (anthocyanin-1) allele of Zea maysFranklin, Tanya Michelle January 1990 (has links)
No description available.
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Delia : a gene regulating pigmentation pattern in Antirrhinum majusGoodrich, Justin January 1992 (has links)
No description available.
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Genetic manipulation of Zea mays LSouthgate, Elizabeth M. January 1996 (has links)
No description available.
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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.
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Evaluation of Argentine maize hybrids and exotic x temperate testcrosses across environmentsOchs, 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.
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Genetic diversity and performance of maize varieties from Zimbabwe, Zambia and MalawiMagorokosho, 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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