128 research outputs found

    Investigation of the ferromagnetic transition in the correlated 4d perovskites SrRu1x_{1-x}Rhx_xO3_3

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    The solid-solution SrRu1x_{1-x}Rhx_xO3_3 (0x10\le x \le1) is a variable-electron-configuration system forming in the nearly-cubic-perovskite basis, ranging from the ferromagnetic 4d4d^4 to the enhanced paramagnetic 4d5d^5. Polycrystalline single-phase samples were obtained over the whole composition range by a high-pressure-heating technique, followed by measurements of magnetic susceptibility, magnetization, specific heat, thermopower, and electrical resistivity. The ferromagnetic order in long range is gradually suppressed by the Rh substitution and vanishes at x0.6x \sim 0.6. The electronic term of specific-heat shows unusual behavior near the critical Rh concentration; the feature does not match even qualitatively with what was reported for the related perovskites (Sr,Ca)RuO3_3. Furthermore, another anomaly in the specific heat was observed at x0.9x \sim 0.9.Comment: Accepted for publication in PR

    Adding tree rings to North America's National Forest Inventories: an essential tool to guide drawdown of atmospheric CO2

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    Tree-ring time series provide long-term, annually resolved information on the growth of trees. When sampled in a systematic context, tree-ring data can be scaled to estimate the forest carbon capture and storage of landscapes, biomes, and-ultimately-the globe. A systematic effort to sample tree rings in national forest inventories would yield unprecedented temporal and spatial resolution of forest carbon dynamics and help resolve key scientific uncertainties, which we highlight in terms of evidence for forest greening (enhanced growth) versus browning (reduced growth, increased mortality). We describe jump-starting a tree-ring collection across the continent of North America, given the commitments of Canada, the United States, and Mexico to visit forest inventory plots, along with existing legacy collections. Failing to do so would be a missed opportunity to help chart an evidence-based path toward meeting national commitments to reduce net greenhouse gas emissions, urgently needed for climate stabilization and repair.Published versio

    Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.

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    Leptin is an adipocyte-secreted hormone, the circulating levels of which correlate closely with overall adiposity. Although rare mutations in the leptin (LEP) gene are well known to cause leptin deficiency and severe obesity, no common loci regulating circulating leptin levels have been uncovered. Therefore, we performed a genome-wide association study (GWAS) of circulating leptin levels from 32,161 individuals and followed up loci reaching P<10(-6) in 19,979 additional individuals. We identify five loci robustly associated (P<5 × 10(-8)) with leptin levels in/near LEP, SLC32A1, GCKR, CCNL1 and FTO. Although the association of the FTO obesity locus with leptin levels is abolished by adjustment for BMI, associations of the four other loci are independent of adiposity. The GCKR locus was found associated with multiple metabolic traits in previous GWAS and the CCNL1 locus with birth weight. Knockdown experiments in mouse adipose tissue explants show convincing evidence for adipogenin, a regulator of adipocyte differentiation, as the novel causal gene in the SLC32A1 locus influencing leptin levels. Our findings provide novel insights into the regulation of leptin production by adipose tissue and open new avenues for examining the influence of variation in leptin levels on adiposity and metabolic health

    Mothers-Offspring Resemblance in Intelligence and Its Relationship to Socioeconomic Status

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    Abstract: Kinship studies have shown that most cognitive ability variances are attributable to genotypic variance. Additionally, kinship correlations are generally increased when tasks that are highly g loaded are considered, a result known as the "Jensen effect". Alternatively, some studies have suggested socioeconomic status as an important factor for explaining differences in cognition. The present study investigated these premises in a sample of 141 mothers (mean age = 36.6; SD = 6.0) and their offspring (53.2% girls; mean age = 11.0; SD = 2.1). The Standard Progressive Matrices of Raven (mothers and offspring) and six other cognitive measures (offspring only) were administered. The findings suggested evidence of g heritability (Jensen effect), which is consistent with published literature on intelligence. However, kinship correlation coefficients were lower (.041 to .177) when compared to other published findings. Finally, the difference between the mother's IQ score and that of her child was influenced by SES and mother's education level

    Genetic insights into resting heart rate and its role in cardiovascular disease.

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    Resting heart rate is associated with cardiovascular diseases and mortality in observational and Mendelian randomization studies. The aims of this study are to extend the number of resting heart rate associated genetic variants and to obtain further insights in resting heart rate biology and its clinical consequences. A genome-wide meta-analysis of 100 studies in up to 835,465 individuals reveals 493 independent genetic variants in 352 loci, including 68 genetic variants outside previously identified resting heart rate associated loci. We prioritize 670 genes and in silico annotations point to their enrichment in cardiomyocytes and provide insights in their ECG signature. Two-sample Mendelian randomization analyses indicate that higher genetically predicted resting heart rate increases risk of dilated cardiomyopathy, but decreases risk of developing atrial fibrillation, ischemic stroke, and cardio-embolic stroke. We do not find evidence for a linear or non-linear genetic association between resting heart rate and all-cause mortality in contrast to our previous Mendelian randomization study. Systematic alteration of key differences between the current and previous Mendelian randomization study indicates that the most likely cause of the discrepancy between these studies arises from false positive findings in previous one-sample MR analyses caused by weak-instrument bias at lower P-value thresholds. The results extend our understanding of resting heart rate biology and give additional insights in its role in cardiovascular disease development
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