199 research outputs found

    Methodologies for generating variability. Part 1: Use of genetic resources in plant breeding

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    Liquid 4He near the superfluid transition in the presence of a heat current and gravity

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    The effects of a heat current and gravity in liquid 4He near the superfluid transition are investigated for temperatures above and below T_lambda. We present a renormalization-group calculation based on model F for the Green's function in a self-consistent approximation which in quantum many-particle theory is known as the Hartree approximation. The approach can handle a zero average order parameter above and below T_lambda and includes effects of vortices. We calculate the thermal conductivity and the specific heat for all temperatures T and heat currents Q in the critical regime. Furthermore, we calculate the temperature profile. Below T_lambda we find a second correlation length which describes the dephasing of the order parameter field due to vortices. We find dissipation and mutual friction of the superfluid-normal fluid counterflow and calculate the Gorter-Mellink coefficient A. We compare our theoretical results with recent experiments.Comment: 26 pages, 9 figure

    Surprising flowering response to photoperiod: Preliminary characterization of West and Central African pearl millet germplasm

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    Pearl millet (Pennisetum glaucum) is considered to be a short-day species that flowers, or flowers earlier, when day lengths are short. A few studies with two to six planting dates and few selected entries have been conducted in USA (Burton 1965), Senegal (Ramond 1968), and India (Patil et al. 1978, Das 1991). However, there is no known research on the flowering response of pearl millet to photoperiod changes over the entire year. Likewise, knowledge about the photoperiod-sensitivity in West and Central African pearl millets is insufficient

    Evaluation of medium maturity, high-tillering Pearl Millet population diallel in Niger

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    Pearl millet [Pennisetum glaucum (L.) R. Br.] is the most important staple crop of millions of people in the semiarid and arid regions of Asia and sub-Saharan Africa. In 1998, ICRISAT pearl millet scientists in southern and western Africa and India initiated global pearl millet diallel crosses with the aim of promoting systematic diversification of elite regional germplasm (Bidinger et al. 2000). The project produced trait-based sets of diallel crosses among elite landrace and breeding materials from each of the three major pearl millet-growing regions. This study evaluates the potential of the medium-maturity, hightillering population diallel as new source material for use in breeding programs in the Sahelian zone of West Africa, especially Niger

    A First-Landau-Level Laughlin/Jain Wave Function for the Fractional Quantum Hall Effect

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    We show that the introduction of a more general closed-shell operator allows one to extend Laughlin's wave function to account for the richer hierarchies (1/3, 2/5, 3/7 ...; 1/5, 2/9, 3/13, ..., etc.) found experimentally. The construction identifies the special hierarchy states with condensates of correlated electron clusters. This clustering implies a single-particle (ls)j algebra within the first Landau level (LL) identical to that of multiply filled LLs in the integer quantum Hall effect. The end result is a simple generalized wave function that reproduces the results of both Laughlin and Jain, without reference to higher LLs or projection.Comment: Revtex. In this replacement we show how to generate the Jain wave function explicitly, by acting with the generalized ls closed-shell operator discussed in the original version. We also walk the reader through a classical 1d caricature of this problem so that he/she can better understand why 2s+1, where s is the spin, should be associated with the number of electrons associated with the underlying clusters or composites. 11 page

    Multiplication and preliminary characterization of west and central African pearl millet landraces

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    West Africa is a center of origin and diversity of pearl millet [Pennisetum glaucum (L.) R. Br.], but this diversity is neither well-understood nor fully accessible to and exploited by NARS breeders and farmers. The objective of the present study was to multiply and initially characterize 281 pearl millet accessions from all over West and Central Africa, with the final aim of promoting a more systematic and targeted exploitation of genetic diversity in adapted germplasm in West African pearl millet improvement programs

    Improved methodologies for breeding striga-resistant sorghums

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    Parasitic flowering weeds of the genus Striga (Scrophulariaceae) cause substantial losses in sorghum [Sorghum bicolor (L.) Moench] production in sub-Saharan Africa. Striga-resistant sorghum cultivars could be a major component of integrated striga management, if resistance was available in adapted, productive germplasm. In this paper we review methodologies for breeding striga-resistant sorghums. The agar-gel assay is an excellent tool to screen host genotypes in the laboratory for low production of the striga seed germination stimulant. Further laboratory assays are needed which allow the non-destructive, rapid and inexpensive evaluation of individual plants for additional resistance mechanisms. Field screening for striga resistance is hampered by high microvariability in African soils, heterogeneity of natural infestations, and concomitant large environmental effects on striga emergence. An improved field testing methodology should include one or several of the following practices: field inoculation with striga seeds; appropriate experimental design including elevated replication number; specific plot layout; use of appropriate susceptible and resistant checks; evaluation in adjacent infested and uninfested plots; and the use of selection indices derived from emerged striga counts, striga vigor, and grain yield or a host plant damage score. Due to the extreme variability of the parasite and significant genotype×environment interaction effects, multi-locational screening is recommended to obtain materials with stable performance. Additional strategies include: careful definition of the target environments; determination of the most important selection traits in each target environment; characterization of crop germplasm and improvement of available sources of resistance for better agronomic performance; transfer and pyramiding of resistance genes into adapted, farmer-selected cultivars; development of striga-resistant parent lines for hybrid or synthetic cultivars; and development of random-mating populations with multiple sources of resistance. The development of marker-assisted selection techniques for broad-based, polygenic striga resistance is underway. This approach is particularly promising because striga resistance tests are difficult, expensive, and sometimes unreliable; the parasite is quarantined; and some resistance genes are recessive. Transgenic, herbicide-tolerant sorghums could contribute to an immediate, cost-effective control of striga by herbicides, but such cultivars are not yet available. The selection of sorghum cultivars with specific adaptation to integrated striga management approaches could contribute to sustainable sorghum production in striga-infested areas of sub-Saharan Afric

    Mechanisms of adaptation to climate variability in West African pearl millet landraces – a preliminary

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    Landraces are generally expected to possess specific mechanisms of adaptation to their growing environments. In West and Central Africa (WCA), growing conditions of pearl millet (Pennisetum glaucum) are characterized, among other hazards, by highly variable beginnings and endings of the rainy season, and unpredictable drought stress at any time during the growing season. Adaptation to such unpredictable variable environment can be due to individual and/or populational buffering (Allard and Bradshaw 1964), two mechanisms initially defined by Lerner (1954) as developmental and genetic homeostasis. Individual buffering may be favored by phenotypic plasticity. Photoperiod-sensitive flowering is an example of phenotypic plasticity that can enhance adaptation to variable planting dates followed due to a scattered beginning of the rainy season in a region, as typical for WCA. It enhances simultaneous flowering of the cultivar in the target region, independent of the individual date of planting in different fields. This has particular advantages in terms of reducing bird damage and insect pressure; prolonging vegetative development in case of early planting but accelerating development in case of late planting; therefore fitting plant development to available rainfall patterns and resulting potentially in increased yielding stability. Populational buffering can be promoted by genetic heterogeneity in plant stand as different genotypes present in the population are specifically adapted to different environmental conditions (Bradshaw 1965). An example is intra-varietal variation for flowering time, which would assure that in case of a dry spell, not all plants in the field will be affected by drought in their most sensitive flowering stage

    Dobrushin states in the \phi^4_1 model

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    We consider the van der Waals free energy functional in a bounded interval with inhomogeneous Dirichlet boundary conditions imposing the two stable phases at the endpoints. We compute the asymptotic free energy cost, as the length of the interval diverges, of shifting the interface from the midpoint. We then discuss the effect of thermal fluctuations by analyzing the \phi^4_1-measure with Dobrushin boundary conditions. In particular, we obtain a nontrivial limit in a suitable scaling in which the length of the interval diverges and the temperature vanishes. The limiting state is not translation invariant and describes a localized interface. This result can be seen as the probabilistic counterpart of the variational convergence of the associated excess free energy.Comment: 34 page

    Selection methods Part 4: Developing open-pollinated varieties using recurrent selection methods

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