Rotational breakup as the origin of small binary asteroids

Asteroids with satellites are observed throughout the Solar System, from subkilometre near-Earth asteroid pairs to systems of large and distant bodies in the Kuiper belt. The smallest and closest systems are found among the near-Earth and small inner main-belt asteroids, which typically have rapidly rotating primaries and close secondaries on circular orbits. About 15 per cent of near-Earth and main-belt asteroids with diameters under 10 km have satellites. The mechanism that forms such similar binaries in these two dynamically different populations was hitherto unclear. Here we show that these binaries are created by the slow spinup of a 'rubble pile' asteroid by means of the thermal YORP (Yarkovsky-O'Keefe-Radzievskii-Paddack) effect. We find that mass shed from the equator of a critically spinning body accretes into a satellite if the material is collisionally dissipative and the primary maintains a low equatorial elongation. The satellite forms mostly from material originating near the primary's surface and enters into a close, low-eccentricity orbit. The properties of binaries produced by our model match those currently observed in the small near-Earth and main-belt asteroid populations, including 1999 KW(4) (refs 3, 4).     

配有钢筋和FRP筋梁的非线性有限元分析

介绍了配有纤维增强复合材料（FRP）筋和普通钢筋梁的非线性有限元分析,结果表明：配有FRP筋梁的强度较仅配钢筋的梁的强度高,2种筋的复合使用可提高梁的延性．     

Mechanisms for the hiatus in global warming

The observed global mean temperature is the highest on record for the past decade but has plateaued to form an apparent ＂hiatus＂ in global temperature rise, with an almost zero short-term trend. Several speakers presented results on the hiatus and suggested possible mechanisms.     

一种基于IP技术的PBX系统

给出了一种基于IP技术的PBX系统的总体方案,重点介绍了呼 管理嚣数据库、用户接口界面、呼叫管理控制和语音信箱的设计和研制,最后给出了测试和实验结果。该PBX系统成成功地实现了南京和香港之间的语音通信。     

A synonymous variant in IRGM alters a binding site for miR-196 and causes deregulation of IRGM-dependent xenophagy in Crohn's disease

Susceptibility to Crohn's disease, a complex inflammatory disease, is influenced by common variants at many loci. The common exonic synonymous SNP (c.313C>T) in IRGM, found in strong linkage disequilibrium with a deletion polymorphism, has been classified as non-causative because of the absence of an alteration in the IRGM protein sequence or splice sites. Here we show that a family of microRNAs (miRNAs), miR-196, is overexpressed in the inflammatory intestinal epithelia of individuals with Crohn's disease and downregulates the IRGM protective variant (c.313C) but not the risk-associated allele (c.313T). Subsequent loss of tight regulation of IRGM expression compromises control of intracellular replication of Crohn's disease-associated adherent invasive Escherichia coli by autophagy. These results suggest that the association of IRGM with Crohn's disease arises from a miRNA-based alteration in IRGM regulation that affects the efficacy of autophagy, thereby implicating a synonymous polymorphism as a likely causal variant.     

Preliminary assessment of velvet ant (Hymenoptera: Mutillidae) diversity in the deserts of southern California

The deserts of southern California house a diverse and unique insect fauna. Velvet ants (Hymenoptera: Mutillidae) are common in these deserts. Velvet ants are important to ecosystem health, particularly in desert environments, because they are parasitic on the bees and wasps that help maintain overall ecosystem function. The goal of this study was to measure velvet ant diversity across the deserts of southern California. We made preliminary collections from 10 sites in a variety of areas in the western Sonoran Desert (Colorado Desert), the Mojave Desert, and the Great Basin Desert. We measured β-diversity using Sørensen’s similarity index to compare velvet ant richness and relative abundance between different sites. To determine how accurate our similarity estimates were, and to gain an understanding of actual velvet ant diversity, we also compared velvet ant richness of 2 sites (Algodones Sand Dunes and Deep Canyon) using data obtained from the examination of museum specimens borrowed from over 12 museums across the West. Comparisons of velvet ant faunas between sites revealed low similarities (0.167–0.75 species richness only; 0.022–0.67 both abundance and richness). Low similarity values indicate that a rich velvet ant fauna exists in the deserts of southern California.     

Genome-wide survey of recurrent HBV integration in hepatocellular carcinoma

To survey hepatitis B virus (HBV) integration in liver cancer genomes, we conducted massively parallel sequencing of 81 HBV-positive and 7 HBV-negative hepatocellular carcinomas (HCCs) and adjacent normal tissues. We found that HBV integration is observed more frequently in the tumors (86.4%) than in adjacent liver tissues (30.7%). Copy-number variations (CNVs) were significantly increased at HBV breakpoint locations where chromosomal instability was likely induced. Approximately 40% of HBV breakpoints within the HBV genome were located within a 1,800-bp region where the viral enhancer, X gene and core gene are located. We also identified recurrent HBV integration events (in ≥ 4 HCCs) that were validated by RNA sequencing (RNA-seq) and Sanger sequencing at the known and putative cancer-related TERT, MLL4 and CCNE1 genes, which showed upregulated gene expression in tumor versus normal tissue. We also report evidence that suggests that the number of HBV integrations is associated with patient survival.     

Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria

We used exome sequencing to identify the genetic basis of combined malonic and methylmalonic aciduria (CMAMMA). We sequenced the exome of an individual with CMAMMA and followed up with sequencing of eight additional affected individuals (cases). This included one individual who was identified and diagnosed by searching an exome database. We identify mutations in ACSF3, encoding a putative methylmalonyl-CoA and malonyl-CoA synthetase as a cause of CMAMMA. We also examined a canine model of CMAMMA, which showed pathogenic mutations in a predicted ACSF3 ortholog. ACSF3 mutant alleles occur with a minor allele frequency of 0.0058 in ～1,000 control individuals, predicting a CMAMMA population incidence of ～1:30,000. ACSF3 deficiency is the first human disorder identified as caused by mutations in a gene encoding a member of the acyl-CoA synthetase family, a diverse group of evolutionarily conserved proteins, and may emerge as one of the more common human metabolic disorders.