Black hole thermodynamics with generalized uncertainty principle

In the standard viewpoint, the temperature of a stationary black hole is proportional to its surface gravity, $T_H=\hbar\kappa/2\pi$. This is a semiclassical result and the quantum gravity effects are not taken into consideration. This Letter explores a unified expression for the black hole temperature in the sense of a generalized uncertainty principle(GUP). Our discussion involves a heuristic analysis of a particle which is absorbed by the black hole. Besides a class of static and spherically symmetric black holes, an axially symmetric Kerr-Newman black hole is considered. Different from the existing literature, we suggest that the black hole's irreducible mass represent the characteristic size in the absorption process. The information capacity of a remnant is also discussed by Bousso's D-bound in de Sitter spacetime.Comment: 18 pages, great improvement on the first version; a Kerr-Newman black hole is considere

The trans-ancestral genomic architecture of glycemic traits

Glycemic traits are used to diagnose and monitor type 2 diabetes and cardiometabolic health. To date, most genetic studies of glycemic traits have focused on individuals of European ancestry. Here we aggregated genome-wide association studies comprising up to 281,416 individuals without diabetes (30% non-European ancestry) for whom fasting glucose, 2-h glucose after an oral glucose challenge, glycated hemoglobin and fasting insulin data were available. Trans-ancestry and single-ancestry meta-analyses identified 242 loci (99 novel; P < 5 x 10(-8)), 80% of which had no significant evidence of between-ancestry heterogeneity. Analyses restricted to individuals of European ancestry with equivalent sample size would have led to 24 fewer new loci. Compared with single-ancestry analyses, equivalent-sized trans-ancestry fine-mapping reduced the number of estimated variants in 99% credible sets by a median of 37.5%. Genomic-feature, gene-expression and gene-set analyses revealed distinct biological signatures for each trait, highlighting different underlying biological pathways. Our results increase our understanding of diabetes pathophysiology by using trans-ancestry studies for improved power and resolution.A trans-ancestry meta-analysis of GWAS of glycemic traits in up to 281,416 individuals identifies 99 novel loci, of which one quarter was found due to the multi-ancestry approach, which also improves fine-mapping of credible variant sets.Diabetes mellitus: pathophysiological changes and therap