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Besides these major land use types, there are a number of specific regionally characterized land uses in Europe.
We characterized land use/land cover over the last three decades by classifying historical multi-temporal Landsat imagery.
Presence is determined by a reciprocal BLASTP hit with an E-value < 1x10-30 or less using the characterized land plant A. thaliana or S. moellendorffii gene as a query, searching the NCBI, JGI, and Congenie databases.
Based on comparisons among all characterized land plants in previously published reports, woody species have a low cpDNA substitution rate, though a limited number of single nucleotide polymorphisms were detected [ 54, 55].
Presence is determined by a reciprocal BLASTP hit with an E-value < 1x10-30 or less using the characterized land plant A. thaliana or S. moellendorffii gene as a query, searching the NCBI, JGI, OIST Marine Genomics Unit (http://marinegenomics.oist.jp/genomes/gallery/) and Paramecium (http://paramecium.cgm.cnrs-gif.fr/) databases.
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We selected and further characterized landing site lines that are well suited for transgenesis and the characterization of regulatory elements.
Recently, a site-specific transgenesis system with characterized landing sites has been reported for zebrafish (Mosimann et al., 2013).
Additionally, we devised a simple technique for constructing arrays of transgenes at a single landing site, thereby extending the utility of previously characterized landing sites.
To distinguish between the effects of PRE sequence and of genomic environment, we generated transgenic reporter fly lines carrying each PRE at four different, precisely characterized, landing sites.
Notably, we isolated and characterized landing site candidates in half as many generations and at significantly reduced fly work compared to the traditional method.
Increasing rates of forest conversion, unsustainable agricultural land use and severe soil erosion are the major factors characterizing land degradation in the highlands of Ethiopia (Mekuria 2005).
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