Carboniferous petroleum systems around the Mid North Sea High, UK

The existence of an extensive, prospective Visean–Namurian Carboniferous petroleum system in and around the hitherto under-explored Mid North Sea High is documented. Evidence is drawn from integrated analysis of over 50,000 line kilometres of seismic data and well data, together with regional source rock screening, reservoir analysis and basin modelling. Visean-Namurian marine and non-marine mudstones and coal source rocks are interbedded within fluvial and marine reservoir sandstones within a stacked succession up to 5 km thick. Source rocks are dominantly gas-prone with oil-prone intervals, and have reached oil to gas maturity levels dependent on location. Burial/thermal history modelling indicates a kitchen area on the southern margin of the Mid North Sea High with northwest and northeastwards migration of gas and oil during Mesozoic and Cenozoic times. A variety of structural and stratigraphic traps are possible, including intraformational Carboniferous traps, with a regional seal at Permian (Zechstein) level. Synthesis of many previously unpublished datasets demonstrates the Visean–Namurian play south of the Mid North Sea High as part of an extensive petroleum system from the East Irish Sea, across onshore to offshore UK and into The Netherlands sector of the North Sea. The purpose of this synthesis is to highlight future exploration opportunities beneath and northwards of the productive Westphalian Southern North Sea gas basin, and to begin to de-risk the petroleum systems that are exemplified by the lower Carboniferous Breagh Field in a frontier area of the mature North Sea province

Electrochemical deposition of zeolitic imidazolate framework electrode coatings for supercapacitor electrodes

Zn and Co electrodes have been successfully coated with five different zeolitic imidazolate frameworks ZIFs (ZIF-4, ZIF-7, ZIF-8, ZIF-14 and ZIF-67) via the anodic dissolution method. Careful control of the reaction conditions allows for electrode coating growth; in contrast to previous reports of electrochemical ZIF growth, which have not succeeded in obtaining ZIF electrode coatings. Coating crystallinity is also shown to be heavily dependent upon reaction conditions, with amorphous rather than crystalline material generated at shorter reaction times and lower linker concentrations. Electrochemical applications for ZIF-coated electrodes are highlighted with the observation of an areal capacitance of 10.45 mF cm−2 at 0.01 V s−1 for additive-free ZIF-67 coated Co electrodes. This is superior to many reported metal organic framework (MOF)/graphene composites and to capacitance values previously reported for additive-free MOFs

Whole-genome sequencing reveals host factors underlying critical COVID-19

Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2,3,4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes—including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)—in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease