1,989 research outputs found
A Cross-Over in the Enstrophy Decay in Two-Dimensional Turbulence in a Finite Box
The numerical simulation of two-dimensional decaying turbulence in a large
but finite box presented in this paper uncovered two physically different
regimes of enstrophy decay. During the initial stage, the enstrophy, generated
by a random Gaussian initial condition, decays as t^{-gamma} with gamma
approximately 0.7-0.8. After that, the flow undergoes a transition to a gas or
fluid composed of distinct vortices. Simultaneously, the magnitude of the decay
exponent crosses over to gamma approximately 0.4. An exact relation for the
total number of vortices, N(t), in terms of the mean circulation of an
individual vortex is derived. A theory predicting that N(t) is proportional to
t^{-xi} and the magnitudes of exponents gamma=2/5 and xi=4/5 is presented and
the possibility of an additional very late-time cross-over to gamma=1/3 and
xi=2/3 is also discussed.Comment: 11 pages, 7 figure
Problematic weed species in organic arable agriculture around the Baltic Sea - an expert database
Weeds are a perpetual challenge in Organic agriculture. However, they serve multiple ecosystem services and a low competitive weed cover can be tolerated. Adding to
this, is the fact that only a few species prove problematic for both the crop and the farmer. The international PRODIVA project researches the effect of crop diversity strategies on the diversity of weed communities, hypothesizing that by increasing the weed diversity, the development of problematic weeds will mitigated. A preparatory
study was conducted to list the most problematic weed species in spring sown cereals in the countries involved with PRODIVA. For this a literature review was conducted in
all participating countries, collecting local sources including grey literature. This was combined with the opinion of local extension services and other weed experts. From this a list of 10 most problematic weeds was deducted for each country. We found both annual and perennial species to be mentioned as problematic. A majority of the
more problematic species were shared between countries, such as Cirsium arvensis, Elitrigia repens and Chenopodium album. Still, all countries revealed to have individual
weed challenges as well. These findings are published as a folder that will be available to local stakeholders
Endothelial Protein C–Targeting Liposomes Show Enhanced Uptake and Improved Therapeutic Efficacy in Human Retinal Endothelial Cells
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MESQUITE design : issues in the development of a mesh quality improvement toolkit.
Poor mesh quality is known to adversely affect both solution efficiency and accuracy. There has been considerable research on a wide variety of mesh improvement algorithms, but the impact of these algorithms on applications has been limited because they are typically embedded in particular meshing software packages. To rectify this situation, they are developing a stand-alone mesh quality improvement toolkit called MESQUITE. In this paper, the authors describe the motivation, goals, and design of MESQUITE and give some computational results using the underlying algorithms that show the benefit of such a package
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
<p>Abstract</p> <p>Background</p> <p>Blood lipid levels including low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), and triglycerides (TG) are highly heritable. Genome-wide association is a promising approach to map genetic loci related to these heritable phenotypes.</p> <p>Methods</p> <p>In 1087 Framingham Heart Study Offspring cohort participants (mean age 47 years, 52% women), we conducted genome-wide analyses (Affymetrix 100K GeneChip) for fasting blood lipid traits. Total cholesterol, HDL-C, and TG were measured by standard enzymatic methods and LDL-C was calculated using the Friedewald formula. The long-term averages of up to seven measurements of LDL-C, HDL-C, and TG over a ~30 year span were the primary phenotypes. We used generalized estimating equations (GEE), family-based association tests (FBAT) and variance components linkage to investigate the relationships between SNPs (on autosomes, with minor allele frequency ≥10%, genotypic call rate ≥80%, and Hardy-Weinberg equilibrium p ≥ 0.001) and multivariable-adjusted residuals. We pursued a three-stage replication strategy of the GEE association results with 287 SNPs (P < 0.001 in Stage I) tested in Stage II (n ~1450 individuals) and 40 SNPs (P < 0.001 in joint analysis of Stages I and II) tested in Stage III (n~6650 individuals).</p> <p>Results</p> <p>Long-term averages of LDL-C, HDL-C, and TG were highly heritable (h<sup>2 </sup>= 0.66, 0.69, 0.58, respectively; each P < 0.0001). Of 70,987 tests for each of the phenotypes, two SNPs had p < 10<sup>-5 </sup>in GEE results for LDL-C, four for HDL-C, and one for TG. For each multivariable-adjusted phenotype, the number of SNPs with association p < 10<sup>-4 </sup>ranged from 13 to 18 and with p < 10<sup>-3</sup>, from 94 to 149. Some results confirmed previously reported associations with candidate genes including variation in the lipoprotein lipase gene (<it>LPL</it>) and HDL-C and TG (rs7007797; P = 0.0005 for HDL-C and 0.002 for TG). The full set of GEE, FBAT and linkage results are posted at the <b>d</b>ata<b>b</b>ase of <b>G</b>enotype <b>a</b>nd <b>P</b>henotype (dbGaP). After three stages of replication, there was no convincing statistical evidence for association (i.e., combined P < 10<sup>-5 </sup>across all three stages) between any of the tested SNPs and lipid phenotypes.</p> <p>Conclusion</p> <p>Using a 100K genome-wide scan, we have generated a set of putative associations for common sequence variants and lipid phenotypes. Validation of selected hypotheses in additional samples did not identify any new loci underlying variability in blood lipids. Lack of replication may be due to inadequate statistical power to detect modest quantitative trait locus effects (i.e., <1% of trait variance explained) or reduced genomic coverage of the 100K array. GWAS in FHS using a denser genome-wide genotyping platform and a better-powered replication strategy may identify novel loci underlying blood lipids.</p
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