Brown Dwarf Jets: Investigating the Universality of Jet Launching Mechanisms at the Lowest Masses

Recently it has become apparent that proto-stellar-like outflow activity extends to the brown dwarf (BD) mass regime. While the presence of accretion appears to be the common ingredient in all objects known to drive jets fundamental questions remain unanswered. The more prominent being the exact mechanism by which jets are launched, and whether this mechanism remains universal among such a diversity of sources and scales. To address these questions we have been investigating outflow activity in a sample of protostellar objects that differ considerably in mass and mass accretion rate. Central to this is our study of brown dwarf jets. To date Classical T Tauri stars (CTTS) have offered us the best touchstone for decoding the launching mechanism. Here we shall summarise what is understood so far of BD jets and the important constraints observations can place on models. We will focus on the comparison between jets driven by objects with central mass < 0.1M \odot and those driven by CTTSs. In particular we wish to understand how the the ratio of the mass outflow to accretion rate compares to what has been measured for CTTSs.Comment: Proceedings of IAU meeting 275, "Jets at All Scales

Disulfoxide Ligands in Rhodium Catalyzed Asymmetric 1,4-Addition: First Studies and Future Directions

Disulfoxides with atropisomeric backbones are introduced as readily available chiral ligands for the rhodium-catalyzed 1,4-addition of arylboronic acids to unsaturated carbonyl compounds. The ligands are obtained in pure form from either commercially available or easily synthesized starting materials. Precatalysts with general formula {(disulfoxide)RhCl}2 were prepared in high yield and were fully characterized. Preliminary results on the influence of steric and electronic modifications of the ligand structure and their impact on the catalytic behavior are presented

Tephra glass chemistry provides storage and discharge details of five magma reservoirs which fed the 75 ka Youngest Toba Tuff eruption, northern Sumatra

The Youngest Toba Tuff contains five distinct glass populations, identified from Ba, Sr and Y compositions, termed PI (lowest Ba) – PV (highest Ba), representing five compositionally distinct pre‐eruptive magma batches that fed the eruption. The PI–PV compositions display systematic changes, with higher FeO, CaO, MgO, TiO₂ and lower incompatible element concentrations in the low‐SiO₂ PIV/PV, than the high‐SiO₂ PI–PIII compositions. Glass shard abundances indicate PIV and PV were the least voluminous magma batches, and PI and PIII the most voluminous. Pressure estimates using rhyolite‐MELTS indicate PV magma equilibrated at ~6 km, and PI magma at ~3.8 km. Glass population proportions in distal tephra and proximal (caldera‐wall) material describe an eruption which commenced by emptying the deepest PIV and PV reservoirs, this being preferentially deposited in a narrow band across southern India (possibly due to jet‐stream and/or plinian eruption transport), and as abundant pumice clasts in the lowermost proximal ignimbrites. Later, shallower magma reservoirs erupted, with PI being the most abundant as the eruption ended, sourcing the majority of distal ash from co‐ignimbrite clouds (PI‐ and PIII‐dominant), where associated ignimbrites isolated earlier (PIV‐ and PV‐rich) deposits. This study shows how analysis of tephra glass compositional data can yield pre‐eruption magma volume estimates, and enable aspects of magma storage conditions and eruption dynamics to be described

Human Neuromuscular Junction on a Chip: Impact of Amniotic Fluid Stem Cell Extracellular Vesicles on Muscle Atrophy and NMJ Integrity

: Neuromuscular junctions (NMJs) are specialized synapses, crucial for the communication between spinal motor neurons (MNs) and skeletal muscle. NMJs become vulnerable in degenerative diseases, such as muscle atrophy, where the crosstalk between the different cell populations fails, and the regenerative ability of the entire tissue is hampered. How skeletal muscle sends retrograde signals to MNs through NMJs represents an intriguing field of research, and the role of oxidative stress and its sources remain poorly understood. Recent works demonstrate the myofiber regeneration potential of stem cells, including amniotic fluid stem cells (AFSC), and secreted extracellular vesicles (EVs) as cell-free therapy. To study NMJ perturbations during muscle atrophy, we generated an MN/myotube co-culture system through XonaTM microfluidic devices, and muscle atrophy was induced in vitro by Dexamethasone (Dexa). After atrophy induction, we treated muscle and MN compartments with AFSC-derived EVs (AFSC-EVs) to investigate their regenerative and anti-oxidative potential in counteracting NMJ alterations. We found that the presence of EVs reduced morphological and functional in vitro defects induced by Dexa. Interestingly, oxidative stress, occurring in atrophic myotubes and thus involving neurites as well, was prevented by EV treatment. Here, we provided and validated a fluidically isolated system represented by microfluidic devices for studying human MN and myotube interactions in healthy and Dexa-induced atrophic conditions-allowing the isolation of subcellular compartments for region-specific analyses-and demonstrated the efficacy of AFSC-EVs in counteracting NMJ perturbations

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

Variability in SARS-CoV-2 susceptibility and COVID-19 disease severity between individuals is partly due to genetic factors. Here, we identify 4 genomic loci with suggestive associations for SARS-CoV-2 susceptibility and 19 for COVID-19 disease severity. Four of these 23 loci likely have an ethnicity-specific component. Genome-wide association study (GWAS) signals in 11 loci colocalize with expression quantitative trait loci (eQTLs) associated with the expression of 20 genes in 62 tissues/cell types (range: 1:43 tissues/gene), including lung, brain, heart, muscle, and skin as well as the digestive system and immune system. We perform genetic fine mapping to compute 99% credible SNP sets, which identify 10 GWAS loci that have eight or fewer SNPs in the credible set, including three loci with one single likely causal SNP. Our study suggests that the diverse symptoms and disease severity of COVID-19 observed between individuals is associated with variants across the genome, affecting gene expression levels in a wide variety of tissue types

Search for dark matter produced in association with bottom or top quarks in √s = 13 TeV pp collisions with the ATLAS detector

A search for weakly interacting massive particle dark matter produced in association with bottom or top quarks is presented. Final states containing third-generation quarks and miss- ing transverse momentum are considered. The analysis uses 36.1 fb−1 of proton–proton collision data recorded by the ATLAS experiment at √s = 13 TeV in 2015 and 2016. No significant excess of events above the estimated backgrounds is observed. The results are in- terpreted in the framework of simplified models of spin-0 dark-matter mediators. For colour- neutral spin-0 mediators produced in association with top quarks and decaying into a pair of dark-matter particles, mediator masses below 50 GeV are excluded assuming a dark-matter candidate mass of 1 GeV and unitary couplings. For scalar and pseudoscalar mediators produced in association with bottom quarks, the search sets limits on the production cross- section of 300 times the predicted rate for mediators with masses between 10 and 50 GeV and assuming a dark-matter mass of 1 GeV and unitary coupling. Constraints on colour- charged scalar simplified models are also presented. Assuming a dark-matter particle mass of 35 GeV, mediator particles with mass below 1.1 TeV are excluded for couplings yielding a dark-matter relic density consistent with measurements

Global wealth disparities drive adherence to COVID-safe pathways in head and neck cancer surgery

Peer reviewe

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

Variability in SARS-CoV-2 susceptibility and COVID-19 disease severity between individuals is partly due to genetic factors. Here, we identify 4 genomic loci with suggestive associations for SARS-CoV-2 susceptibility and 19 for COVID-19 disease severity. Four of these 23 loci likely have an ethnicity-specific component. Genome-wide association study (GWAS) signals in 11 loci colocalize with expression quantitative trait loci (eQTLs) associated with the expression of 20 genes in 62 tissues/cell types (range: 1:43 tissues/gene), including lung, brain, heart, muscle, and skin as well as the digestive system and immune system. We perform genetic fine mapping to compute 99% credible SNP sets, which identify 10 GWAS loci that have eight or fewer SNPs in the credible set, including three loci with one single likely causal SNP. Our study suggests that the diverse symptoms and disease severity of COVID-19 observed between individuals is associated with variants across the genome, affecting gene expression levels in a wide variety of tissue types