Evidence for an impact-induced biosphere from the δ34S signature of sulphides in the Rochechouart impact structure, France

The highly eroded 23 km diameter Rochechouart impact structure, France, has extensive evidence for post-impact hydrothermal alteration and sulphide mineralization. The sulphides can be divided into four types on the basis of their mineralogy and host rock. They range from pyrites and chalcopyrite in the underlying coherent crystalline basement to pyrites hosted in the impactites. Sulphur isotopic results show that δ34S values vary over a wide range, from -35.8‰ to +0.4‰. The highest values, δ34S -3.7‰ to +0.4‰, are recorded in the coherent basement, and likely represent a primary terrestrial sulphur reservoir. Sulphides with the lowest values, δ34S -35.8‰ to -5.2‰, are hosted within locally brecciated and displaced parautochthonous and autochthonous impactites. Intermediate δ34S values of -10.7‰ to -1.2‰ are recorded in the semi-continuous monomict lithic breccia unit, differing between carbonate-hosted sulphides and intraclastic and clastic matrix-hosted sulphides. Such variable isotope values are consistent with a biological origin, via bacterial sulphate reduction, for sulphides in the parautochthonous and autochthonous units; these minerals formed in the shallow subsurface and are probably related to the post impact hydrothermal system. The source of the sulphate is likely to have been seawater, penecontemporaneous to the impact, as inferred from the marginal marine paleogeography of the structure. In other eroded impact craters that show evidence for impact-induced hydrothermal circulation, indirect evidence for life may be sought isotopically within late-stage (≤120°C) secondary sulphides and within the shocked and brecciated basement immediately beneath the transient crater floor

Stable Isotope Studies of the Rochechouart Impact Structure: Sources of Secondary Carbonates and Sulphides within Allochthonous and Parautochthonous Impactites

Hypervelocity impacts are among the most ubiquitous processes to affect solid bodies within our solar system [1, 2]. Although they are notoriously devastating, citing responsibility for mass extinction events and global climate perturbations, impacts can also create temporary environments which are favorable for life to thrive, if there is enough water present in the target, and sufficient energy is released as heat [1, 2]. One-third of impact structures on Earth contain fossil impact-initiated hydrothermal systems, and they are therefore being explored as potential “cradles of life” on other solid planets and satellites in our solar system [1].<p></p> We are presenting a case for the evaluation of the Mesozoic Rochechouart impact structure in France as a once-habitable environment. Initial δ 13C, δ18O and δ 34S isotope data collected in 2014 from hydrothermal carbonates and sulphides within monomict lithic impact breccia, collected from a site located 7.5km from the center of the structure at Champagnac quarry, supports our hypothesis of a warm, wet environment; we also found evidence for metabolically reduced sulphate [3]. Similar mineral assemblages can be found throughout the structure, including allochthonous breccias and low to unshocked target material. In order to explore our hypothesis further, a larger sample set was collected from various lithologies within the Champagnac site containing sulphide and carbonate mineralization for δ 13C, δ18O and δ34S isotope analysis in January 2015. These results will allow us to determine the relationships between the many hydrothermal mineral assemblages within this area of the structure, and ask whether the isotopic compositions recorded in secondary sulphides and carbonates of the impactites are inherited from the target, or possibly represent colonization by thermophilic microbes during the post-impact hydrothermal period.<p></p&gt

Endothelin-Converting Enzyme-1 (ECE-1) Is Post-Transcriptionally Regulated by Alternative Polyadenylation

Endothelin-converting enzyme-1 (ECE-1) is the enzyme predominantly responsible for producing active endothelin-1 (ET-1), a mitogenic peptide implicated in the aetiology of a number of diseases, including cancer. Elevated levels of ECE-1 have been observed in a range of malignancies, with high expression conferring poor prognosis and aiding the acquisition of androgen independence in prostate cancer. The mechanisms regulating the expression of ECE-1 in cancer cells are poorly understood, hampering the development of novel therapies targeting the endothelin axis. Here we provide evidence that the expression of ECE-1 is markedly inhibited by its 3′UTR, and that alternative polyadenylation (APA) results in the production of ECE-1 transcripts with truncated 3′UTRs which promote elevated protein expression. Abolition of the ECE-1 APA sites reduced protein expression from a reporter vector in prostate cancer cells, suggesting these sites are functional. This is the first study to identify ECE-1 as a target for APA, a regulatory mechanism aberrantly activated in cancer cells, and provides novel information about the mechanisms leading to ECE-1 overexpression in malignant cells

Supporting security-oriented, inter-disciplinary research: crossing the social, clinical and geospatial domains

How many people have had a chronic disease for longer than 5-years in Scotland? How has this impacted upon their choices of employment? Are there any geographical clusters in Scotland where a high-incidence of patients with such long-term illness can be found? How does the life expectancy of such individuals compare with the national averages? Such questions are important to understand the health of nations and the best ways in which health care should be delivered and measured for their impact and success. In tackling such research questions, e-Infrastructures need to provide tailored, secure access to an extensible range of distributed resources including primary and secondary e-Health clinical data; social science data, and geospatial data sets amongst numerous others. In this paper we describe the security models underlying these e-Infrastructures and demonstrate their implementation in supporting secure, federated access to a variety of distributed and heterogeneous data sets exploiting the results of a variety of projects at the National e-Science Centre (NeSC) at the University of Glasgow

Improved silicon quantum dots single electron transfer operation with hydrogen silsesquioxane resist technology

Hydrogen silsesquioxane (HSQ) is a high resolution electron beam resist that offers a high etch resistance and small line edge roughness. In our previous work, we showed that by using this resist we can fabricate very high density double quantum dot (QD) single electron transistors on silicon-on-insulator (SOI) substrates for applications in quantum information processing. We observed that 80% of 144 fabricated devices had dimensional variations of ±5 nm with a standard deviation of 3.4 nm. Here, we report on the functionality of our Si QD devices through electrical measurements and further HSQ process optimisations, which improve the effective side gates control on single electron operation

Design and fabrication of densely integrated silicon quantum dots using a VLSI compatible hydrogen silsesquioxane electron beam lithography process

Hydrogen silsesquioxane (HSQ) is a high resolution negative-tone electron beam resist allowing for direct transfer of nanostructures into silicon-on-insulator. Using this resist for electron beam lithography, we fabricate high density lithographically defined Silicon double quantum dot (QD) transistors. We show that our approach is compatible with very large scale integration, allowing for parallel fabrication of up to 144 scalable devices. HSQ process optimisation allowed for realisation of reproducible QD dimensions of 50 nm and tunnel junction down to 25 nm. We observed that 80% of the fabricated devices had dimensional variations of less than 5 nm. These are the smallest high density double QD transistors achieved to date. Single electron simulations combined with preliminary electrical characterisations justify the reliability of our device and process

PARP1 gene variation and microglial activity on [11C]PBR28 PET in older adults at risk for Alzheimer's disease

Increasing evidence suggests that inflammation is one pathophysio-logical mechanism in Alzheimer's disease (AD). Recent studies have identified an association between the poly (ADP-ribose) polymerase 1 (PARP1) gene and AD. This gene encodes a protein that is involved in many biological functions, including DNA repair and chromatin remodeling, and is a mediator of inflammation. Therefore, we performed a targeted genetic association analysis to investigate the relationship between the PARP1 polymorphisms and brain micro-glial activity as indexed by [11C]PBR28 positron emission tomography (PET). Participants were 26 non-Hispanic Caucasians in the Indiana Memory and Aging Study (IMAS). PET data were intensity-normalized by injected dose/total body weight. Average PBR standardized uptake values (SUV) from 6 bilateral regions of interest (thalamus, frontal, parietal, temporal, and cingulate cortices, and whole brain gray matter) were used as endophenotypes. Single nucleotide polymorphisms (SNPs) with 20% minor allele frequency that were within +/− 20 kb of the PARP1 gene were included in the analyses. Gene-level association analyses were performed using a dominant genetic model with translocator protein (18-kDa) (TSPO) genotype, age at PET scan, and gender as covariates. Analyses were performed with and without APOE ε4 status as a covariate. Associations with PBR SUVs from thalamus and cingulate were significant at corrected p<0.014 and <0.065, respectively. Subsequent multi-marker analysis with cingulate PBR SUV showed that individuals with the “C” allele at rs6677172 and “A” allele at rs61835377 had higher PBR SUV than individuals without these alleles (corrected P<0.03), and individuals with the “G” allele at rs6677172 and “G” allele at rs61835377 displayed the opposite trend (corrected P<0.065). A previous study with the same cohort showed an inverse relationship between PBR SUV and brain atrophy at a follow-up visit, suggesting possible protective effect of microglial activity against cortical atrophy. Interestingly, all 6 AD and 2 of 3 LMCI participants in the current analysis had one or more copies of the “GG” allele combination, associated with lower cingulate PBR SUV, suggesting that this gene variant warrants further investigation