Numerical modelling of heat generation in porous planetesimal collisions

An important unanswered question in planetary science is how planetesimals, the ~1–100 km solid precursors to asteroids and planets, were heated in the early Solar System. This thesis quantifies one possible heat source: planetesimal collisions. Recent work has predicted that collision velocities and planetesimal porosities were likely to have been higher than previously thought; this is likely to have significant implications on collision heating. The approach adopted in this research was to numerically model shock heating during planetesimal collisions. Simulations showed that an increase in porosity can significantly increase heating: in a 5 km s-1 collision between equal sized, non-porous planetesimals, no material was heated to the solidus, compared to two thirds of the mass of 50% porous planetesimals. Velocity also strongly influences heating: at 4 km s-1, an eighth of the mass of 50% porous planetesimals was heated to the solidus, compared to the entire mass at 6 km s-1. Further simulations quantified the influence on heating of the impactor-to-target mass ratio, the initial planetesimal temperature and the impact angle. A Monte Carlo model was developed to examine the cumulative heating caused by a population of impactors striking a parent body. In the majority of collisions the impactor was much smaller than the parent body, and only minor heating was possible. However, some larger or faster impactors were capable of causing significant heating without disrupting the parent body; these collisions could have heated up to 10% of the parent body to the solidus. To cause global heating, the collision must have catastrophically disrupted the parent body. The increase in specific internal energy from collisions was compared with the decay of short-lived radionuclides. In the first ~6 Ma, radioactive decay was the most important heat source. After ~10 Ma, the energy caused by collisions was likely to have overtaken radioactive decay as the dominant source

Genome sequence of an alphaherpesvirus from a beluga whale (Delphinapterus leucas)

Beluga whale alphaherpesvirus 1 was isolated from a blowhole swab taken from a juvenile beluga whale. The genome is 144,144 bp in size and contains 86 putative genes. The virus groups phylogenetically with members of the genus Varicellovirus in subfamily Alphaherpesvirinae and is the first alphaherpesvirus sequenced from a marine mammal

Genome sequence of a gammaherpesvirus from a common bottlenose dolphin (Tursiops truncatus)

A herpesvirus genome was sequenced directly from a biopsy specimen of a rectal lesion from a female common bottlenose dolphin. This genome sequence comprises a unique region (161,235 bp) flanked by multiple copies of a terminal repeat (4,431 bp) and contains 72 putative genes. The virus was named common bottlenose dolphin gammaherpesvirus 1

Scientific mindfulness: a foundation for future themes in international business

We conceptualize new ways to qualify what themes should dominate the future IB research agenda by examining three questions: Whom should we ask? What should we ask and which selection criteria should we apply? What are the contextual forces? We propose scientific mindfulness as the way forward for generating themes in IB research

Cohomological Donaldson-Thomas theory of a quiver with potential and quantum enveloping algebras

This paper concerns the cohomological aspects of Donaldson-Thomas theory for Jacobi algebras and the associated cohomological Hall algebra, introduced by Kontsevich and Soibelman. We prove the Hodge-theoretic categorification of the integrality conjecture and the wall crossing formula, and furthermore realise the isomorphism in both of these theorems as Poincar\'e-Birkhoff-Witt isomorphisms for the associated cohomological Hall algebra. We do this by defining a perverse filtration on the cohomological Hall algebra, a result of the "hidden properness" of the semisimplification map from the moduli stack of semistable representations of the Jacobi algebra to the coarse moduli space of polystable representations. This enables us to construct a degeneration of the cohomological Hall algebra, for generic stability condition and fixed slope, to a free supercommutative algebra generated by a mixed Hodge structure categorifying the BPS invariants. As a corollary of this construction we furthermore obtain a Lie algebra structure on this mixed Hodge structure - the Lie algebra of BPS invariants - for which the entire cohomological Hall algebra can be seen as the positive part of a Yangian-type quantum group.Comment: v5 final version, 64 pages, to appear in Invent. Math. Many thanks to the anonymous referee for helpful suggestion

Discovery and validation of cell cycle arrest biomarkers in human acute kidney injury

Introduction Acute kidney injury (AKI) can evolve quickly and clinical measures of function often fail to detect AKI at a time when interventions are likely to provide benefit. Identifying early markers of kidney damage has been difficult due to the complex nature of human AKI, in which multiple etiologies exist. The objective of this study was to identify and validate novel biomarkers of AKI. Methods We performed two multicenter observational studies in critically ill patients at risk for AKI - discovery and validation. The top two markers from discovery were validated in a second study (Sapphire) and compared to a number of previously described biomarkers. In the discovery phase, we enrolled 522 adults in three distinct cohorts including patients with sepsis, shock, major surgery, and trauma and examined over 300 markers. In the Sapphire validation study, we enrolled 744 adult subjects with critical illness and without evidence of AKI at enrollment; the final analysis cohort was a heterogeneous sample of 728 critically ill patients. The primary endpoint was moderate to severe AKI (KDIGO stage 2 to 3) within 12 hours of sample collection. Results Moderate to severe AKI occurred in 14% of Sapphire subjects. The two top biomarkers from discovery were validated. Urine insulin-like growth factor-binding protein 7 (IGFBP7) and tissue inhibitor of metalloproteinases-2 (TIMP-2), both inducers of G1 cell cycle arrest, a key mechanism implicated in AKI, together demonstrated an AUC of 0.80 (0.76 and 0.79 alone). Urine [TIMP-2]·[IGFBP7] was significantly superior to all previously described markers of AKI (P \u3c0.002), none of which achieved an AUC \u3e0.72. Furthermore, [TIMP-2]·[IGFBP7] significantly improved risk stratification when added to a nine-variable clinical model when analyzed using Cox proportional hazards model, generalized estimating equation, integrated discrimination improvement or net reclassification improvement. Finally, in sensitivity analyses [TIMP-2]·[IGFBP7] remained significant and superior to all other markers regardless of changes in reference creatinine method. Conclusions Two novel markers for AKI have been identified and validated in independent multicenter cohorts. Both markers are superior to existing markers, provide additional information over clinical variables and add mechanistic insight into AKI. Trial registration ClinicalTrials.gov number NCT01209169

Momentum Enhancement during Kinetic Impacts in the Low-intermediate-strength Regime: Benchmarking and Validation of Impact Shock Physics Codes

In 2022 September, the DART spacecraft (NASA’s contribution to the Asteroid Impact & Deflection Assessment (AIDA) collaboration) will impact the asteroid Dimorphos, the secondary in the Didymos system. The crater formation and material ejection will affect the orbital period. In 2027, Hera (ESA’s contribution to AIDA) will investigate the system, observe the crater caused by DART, and characterize Dimorphos. Before Hera’s arrival, the target properties will not be well-constrained. The relationships between observed orbital change and specific target properties are not unique, but Hera’s observations will add additional constraints for the analysis of the impact event, which will narrow the range of feasible target properties. In this study, we use three different shock physics codes to simulate momentum transfer from impactor to target and investigate the agreement between the results from the codes for well-defined target materials. In contrast to previous studies, care is taken to use consistent crushing behavior (e.g., distension as a function of pressure) for a given porosity for all codes. First, we validate the codes against impact experiments into a regolith simulant. Second, we benchmark the codes at the DART impact scale for a range of target material parameters (10%–50% porosity, 1.4–100 kPa cohesion). Aligning the crushing behavior improves the consistency of the derived momentum enhancement between the three codes to within +/−5% for most materials used. Based on the derived mass–velocity distributions from all three codes, we derive scaling parameters that can be used for studies of the ejecta curtain

Oxidative dearomatisation: the key step of sorbicillinoid biosynthesis

An FAD-dependent monooxygenase encoding gene (SorbC) was cloned from Penicillium chrysogenum E01-10/3 and expressed as a soluble protein in Escherichia coli. The enzyme efficiently performed the oxidative dearomatisation of sorbicillin and dihydrosorbicillin to give sorbicillinol and dihydrosorbicillinol respectively. Bioinformatic examination of the gene cluster surrounding SorbC indicated the presence of two polyketide synthase (PKS) encoding genes designated sorbA and sorbB. The gene sorbA-encodes a highly reducing iterative PKS while SorbB encodes a non-reducing iterative PKS which features a reductive release domain usually involved in the production of polyketide aldehydes. Using these observations and previously reported results from isotopic feeding experiments a new and simpler biosynthetic route to the sorbicillin class of secondary metabolites is proposed which is consistent with all reported experimental results.Al Baha University, Saudi ArabiaEP/F066104/1BB/I003355/1BMBFERASMUS programm