Initial characterization of a highly contaminated high explosives outfall in preparation for in situ bioremediation

In situ bioremediation is a viable, cost-effective treatment for environmental contamination of many kinds. The feasibility of using biological techniques to remediate soils contaminated with high explosives (HE) requires laboratory evaluation before proceeding to a larger scale field operation. Laboratory investigations have been conducted at pilot scale which indicate that an anaerobic process could be successful at reducing levels of HE, primarily HMX, RDX and TNT, in contaminated soils. A field demonstration project has been designed to create an anaerobic environment for the degradation of HE materials. The first step in this project, initial characterization of the test area, was conducted and is the subject of this report. The levels of HE compounds found in the samples from the test area were higher than the EPA Method 8330 was able to extract without subsequent re-precipitation; therefore, a new method was developed using a superior extractant system. The test area sampling design was relatively simple as one might expect in an initial characterization. A total of 60 samples were each removed to a depth of 4 inches using a 1 inch diameter corer. The samples were spaced at relatively even intervals across a 20 foot cross-section through the middle of four 7-foot-long adjacent plots which are designed to be a part of an in situ bioremediation experiment. Duplicate cores were taken from each location for HE extraction and analysis in order to demonstrate and measure the heterogeneity of the contamination. Each soil sample was air dried and ball-milled to provide a homogeneous solid for extraction and analysis. Several samples had large consolidated pieces of what appeared to be solid HE. These were not ball-milled due to safety concerns, but were dissolved and the solutions were analyzed. The new extraction method was superior in that results obtained for several of the contaminants were up to 20 times those obtained with the EPA extraction method. The results obtained from this study showed that the test area contamination is extremely heterogeneous, and that it contains extremely high levels of the three major contaminants, HMX, RDX and TNT. The potential for success of a bioremediation strategy is discussed

The genetic architecture of the human cerebral cortex

The cerebral cortex underlies our complex cognitive capabilities, yet little is known about the specific genetic loci that influence human cortical structure. To identify genetic variants that affect cortical structure, we conducted a genome-wide association meta-analysis of brain magnetic resonance imaging data from 51,665 individuals. We analyzed the surface area and average thickness of the whole cortex and 34 regions with known functional specializations. We identified 199 significant loci and found significant enrichment for loci influencing total surface area within regulatory elements that are active during prenatal cortical development, supporting the radial unit hypothesis. Loci that affect regional surface area cluster near genes in Wnt signaling pathways, which influence progenitor expansion and areal identity. Variation in cortical structure is genetically correlated with cognitive function, Parkinson's disease, insomnia, depression, neuroticism, and attention deficit hyperactivity disorder

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead