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Investigation of the nucleation and growth of thin-film phosphors
The deposition of CaGa{sub 2}S{sub 4}:Ce has been accomplished using a commercial liquid delivery system on two substrate surfaces: ZnS and SrS. However, the film deposited on ZnS was not of satisfactory quality because of the formation of an amorphous layer and a high amount of residual porosity within the deposition. The use of a SrS layer on top of the ZnS improved the nucleation by reducing the interfacial energy between the substrate and deposition. It greatly reduced the porosity in the coating and reduced the formation of the amorphous layer. The crystallinity of the CaGa{sub 2}S{sub 4} 400 peak was also increased by a factor of ten when a layer of SrS was used. Further, the FWHM of the 400 peaks from the two depositions was not significantly different, indicating that the crystallite size and strain was approximately the same. The B{sub 40} was increased by a factor of two, from 1.84 cd/m{sup 2} for ZnS to 3.67 cd/m{sup 2} for SrS. This increase is an improvement in the performance of the films and is attributable to the increase in the crystallinity
Author Correction: Widespread long-range cis-regulatory elements in the maize genome.
An amendment to this paper has been published and can be accessed via a link at the top of the paper
Widespread long-range cis-regulatory elements in the maize genome.
Genetic mapping studies on crops suggest that agronomic traits can be controlled by gene–distal intergenic loci. Despite the biological importance and the potential agronomic utility of these loci, they remain virtually uncharacterized in all crop species to date. Here, we provide genetic, epigenomic and functional molecular evidence to support the widespread existence of gene–distal (hereafter, distal) loci that act as long-range transcriptional cis-regulatory elements (CREs) in the maize genome. Such loci are enriched for euchromatic features that suggest their regulatory functions. Chromatin loops link together putative CREs with genes and recapitulate genetic interactions. Putative CREs also display elevated transcriptional enhancer activities, as measured by self-transcribing active regulatory region sequencing. These results provide functional support for the widespread existence of CREs that act over large genomic distances to control gene expression
Pines
Pinus is the most important genus within the Family Pinaceae and also within the gymnosperms by the number of species (109 species recognized by Farjon 2001) and by its contribution to forest ecosystems. All pine species are evergreen trees or shrubs. They are widely distributed in the northern hemisphere, from tropical areas to northern areas in America and Eurasia. Their natural range reaches the equator only in Southeast Asia. In Africa, natural occurrences are confined to the Mediterranean basin. Pines grow at various elevations from sea level (not usual in tropical areas) to highlands. Two main regions of diversity are recorded, the most important one in Central America (43 species found in Mexico) and a secondary one in China. Some species have a very wide natural range (e.g., P. ponderosa, P. sylvestris). Pines are adapted to a wide range of ecological conditions: from tropical (e.g., P. merkusii, P. kesiya, P. tropicalis), temperate (e.g., P. pungens, P. thunbergii), and subalpine (e.g., P. albicaulis, P. cembra) to boreal (e.g., P. pumila) climates (Richardson and Rundel 1998, Burdon 2002). They can grow in quite pure stands or in mixed forest with other conifers or broadleaved trees. Some species are especially adapted to forest fires, e.g., P. banksiana, in which fire is virtually essential for cone opening and seed dispersal. They can grow in arid conditions, on alluvial plain soils, on sandy soils, on rocky soils, or on marsh soils. Trees of some species can have a very long life as in P. longaeva (more than 3,000 years)