Household vulnerability and resilience to shocks: findings from Solomon Islands and Vanuatu

"This paper examines the vulnerability and resilience of Pacific Island Countries (PICs) to shock at a national level before presenting the findings of research conducted at the household level in two Melanesian countries: Solomon Islands and Vanuatu.1 PICs represent a diverse group of countries, but they are often referred to as being among the most vulnerable in the world. This reflects both their considerable exposure to the effects of natural hazards and economic shocks as well as their limited ability to manage them (Naudé et al. 2009; Guillaumont, 2010). As small and highly open economies, PICs are highly exposed to volatility in international commodity prices and global economic downturns ..." - page 1AusAIDAustralian Development Research Awar

UTILISING TECHNOLOGIES FOR POST-COVID MULTIMODAL COURSE ENGAGEMENT: AN INITIAL STUDY

In 2020, new undergraduate courses were developed, each with three 4-week modules. In particular, Modern Physics II was developed for a combined roster consisting of both Newcastle and James Cook University students and comprising Special Relativity, Nuclear and Particle Physics modules. To enable maximum engagement, a flipped classroom regime with no lecture notes, blended and remote laboratories and the inclusion of the SLACK project management hub was employed. Students were tasked with creating their own digital lecture notes from online videos resulting in 100% active engagement with the lecture content. All lecturettes contained embedded questions and a comparison of lightboard and PowerPoint was conducted. Weekly, online tutorial workshops using Zoom culminated with over 85% attendance rate consistently throughout the course. A weekly blackboard quiz was performed at a random time during these workshops and based on the embedded lecturette questions. New innovative STEM laboratory workshops were constructed in a variety of active engagement, from purely online worksheets, blended and remote experiments which were developed to work seamlessly under the changing COVID-19 restrictions. Students were exposed to planning, management and python control coding under the visage of “embracing technology and best practice to deliver the greatest possible student experience”

Miscellaneous personal letters of Alex Lachlan Williams, 1894-1897

Miscellaneous personal letters from Geoffrey J. Judge of Zeehan in regard to repairs to T. Gibbins' shop, lack of mining jobs and mines "commencing to look up" dated 1 July and 19 August 1894. From James Duncan regarding the tenancy of Williams' property at Zeehan dated 12 September 1896. From Ada Proctor of Sandy Bay on hearing ALW was about to leave Hobart to thank him for all he did for her Aunt dated 29 August 1897. From E.A Lorkin of North Lyell regarding the lease, amalgamation, and section not complying with labour clause written on 18 October 1897. From J. McDonald of Strahan, correspondence regarding mill timber and accompanying list of measurements of logs dated 6 September 1897. These personal letters of Alex Lachlan Williams 1894-1897 are from the papers of Oscar Jones, solicitor of Murdoch & Jones Queenstown branch and his predecessor Alex Lachlan Williams, apparently found at Strathelie at Broadmarsh formerly the Jones family home. The Queenstown practice was established by Alex Lachlan Williams in 1896. Later Charles Page became a partner and established an office at Zeehan. George Murdoch of the Stone Buildings, Hobart, later Murdoch and Jones, acted as Hobart agent and early in 1898 the two firms merged as Williams and Page of Hobart, Queenstown and Zeehan. In April 1899, however, Williams sold out to Murdoch and Jones, Oscar Jones managed the Queenstown branch and by July the firm's name was changed to Murdoch & Jones. Williams & Page remained in Zeehan, under C.S. Page. Private Deposit Collection M14/13 1-

Assessment of Haemodynamic Response to Nonselective Beta-Blockers in Portal Hypertension by Phase-Contrast Magnetic Resonance Angiography

A significant unmet need exists for accurate, reproducible, noninvasive diagnostic tools to assess and monitor portal hypertension (PHT). We report the first use of quantitative MRI markers for the haemodynamic assessment of nonselective beta-blockers (NSBB) in PHT. In a randomized parallel feasibility study in 22 adult patients with PHT and a clinical indication for NSBB, we acquired haemodynamic data at baseline and after 4 weeks of NSBB (propranolol or carvedilol) using phase-contrast MR angiography (PC-MRA) in selected intra-abdominal vessels. T1 mapping of liver and spleen was undertaken to assess changes in tissue composition. Target NSBB dose was achieved in 82%. There was a substantial reduction from baseline in mean average flow in the superior abdominal aorta after 4 weeks of NSBB therapy (4.49±0.98 versus 3.82±0.86 L/min, P=0.03) but there were no statistically significant differences in flow in any other vessels, even in patients with >25% decrease in heart rate (47% of patients). Mean percentage change in liver and spleen T1 following NSBB was small and highly variable. In conclusion, PC-MRA was able to detect reduction in cardiac output by NSBB but did not detect significant changes in visceral blood flow or T1. This trial was registered with the ISRCTN registry (ISRCTN98001632)

A clinically relevant sheep model of orthotopic heart transplantation 24 h after donor brainstem death

BACKGROUND: Heart transplantation (HTx) from brainstem dead (BSD) donors is the gold-standard therapy for severe/end-stage cardiac disease, but is limited by a global donor heart shortage. Consequently, innovative solutions to increase donor heart availability and utilisation are rapidly expanding. Clinically relevant preclinical models are essential for evaluating interventions for human translation, yet few exist that accurately mimic all key HTx components, incorporating injuries beginning in the donor, through to the recipient. To enable future assessment of novel perfusion technologies in our research program, we thus aimed to develop a clinically relevant sheep model of HTx following 24 h of donor BSD. METHODS: BSD donors (vs. sham neurological injury, 4/group) were hemodynamically supported and monitored for 24 h, followed by heart preservation with cold static storage. Bicaval orthotopic HTx was performed in matched recipients, who were weaned from cardiopulmonary bypass (CPB), and monitored for 6 h. Donor and recipient blood were assayed for inflammatory and cardiac injury markers, and cardiac function was assessed using echocardiography. Repeated measurements between the two different groups during the study observation period were assessed by mixed ANOVA for repeated measures. RESULTS: Brainstem death caused an immediate catecholaminergic hemodynamic response (mean arterial pressure, p = 0.09), systemic inflammation (IL-6 - p = 0.025, IL-8 - p = 0.002) and cardiac injury (cardiac troponin I, p = 0.048), requiring vasopressor support (vasopressor dependency index, VDI, p = 0.023), with normalisation of biomarkers and physiology over 24 h. All hearts were weaned from CPB and monitored for 6 h post-HTx, except one (sham) recipient that died 2 h post-HTx. Hemodynamic (VDI - p = 0.592, heart rate - p = 0.747) and metabolic (blood lactate, p = 0.546) parameters post-HTx were comparable between groups, despite the observed physiological perturbations that occurred during donor BSD. All p values denote interaction among groups and time in the ANOVA for repeated measures. CONCLUSIONS: We have successfully developed an ovine HTx model following 24 h of donor BSD. After 6 h of critical care management post-HTx, there were no differences between groups, despite evident hemodynamic perturbations, systemic inflammation, and cardiac injury observed during donor BSD. This preclinical model provides a platform for critical assessment of injury development pre- and post-HTx, and novel therapeutic evaluation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40635-021-00425-4

The 6dF Galaxy Survey: z \approx 0 measurement of the growth rate and sigma_8

We present a detailed analysis of redshift-space distortions in the two-point correlation function of the 6dF Galaxy Survey (6dFGS). The K-band selected sub-sample which we employ in this study contains 81971 galaxies distributed over 17000deg^2 with an effective redshift z = 0.067. By modelling the 2D galaxy correlation function, xi(r_p,pi), we measure the parameter combination f(z)sigma_8(z) = 0.423 +/- 0.055. Alternatively, by assuming standard gravity we can break the degeneracy between sigma_8 and the galaxy bias parameter, b. Combining our data with the Hubble constant prior from Riess et al (2011), we measure sigma_8 = 0.76 +/- 0.11 and Omega_m = 0.250 +/- 0.022, consistent with constraints from other galaxy surveys and the Cosmic Microwave Background data from WMAP7. Combining our measurement of fsigma_8 with WMAP7 allows us to test the relationship between matter and gravity on cosmic scales by constraining the growth index of density fluctuations, gamma. Using only 6dFGS and WMAP7 data we find gamma = 0.547 +/- 0.088, consistent with the prediction of General Relativity. We note that because of the low effective redshift of 6dFGS our measurement of the growth rate is independent of the fiducial cosmological model (Alcock-Paczynski effect). We also show that our conclusions are not sensitive to the model adopted for non-linear redshift-space distortions. Using a Fisher matrix analysis we report predictions for constraints on fsigma_8 for the WALLABY survey and the proposed TAIPAN survey. The WALLABY survey will be able to measure fsigma_8 with a precision of 4-10%, depending on the modelling of non-linear structure formation. This is comparable to the predicted precision for the best redshift bins of the Baryon Oscillation Spectroscopic Survey (BOSS), demonstrating that low-redshift surveys have a significant role to play in future tests of dark energy and modified gravity.Comment: 17 pages, 13 figures, 1 tabl

Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex

The two hemispheres of the human brain differ functionally and structurally. Despite over a century of research, the extent to which brain asymmetry is influenced by sex, handedness, age, and genetic factors is still controversial. Here we present the largest ever analysis of subcortical brain asymmetries, in a harmonized multi-site study using meta-analysis methods. Volumetric asymmetry of seven subcortical structures was assessed in 15,847 MRI scans from 52 datasets worldwide. There were sex differences in the asymmetry of the globus pallidus and putamen. Heritability estimates, derived from 1170 subjects belonging to 71 extended pedigrees, revealed that additive genetic factors influenced the asymmetry of these two structures and that of the hippocampus and thalamus. Handedness had no detectable effect on subcortical asymmetries, even in this unprecedented sample size, but the asymmetry of the putamen varied with age. Genetic drivers of asymmetry in the hippocampus, thalamus and basal ganglia may affect variability in human cognition, including susceptibility to psychiatric disorders

Novel genetic loci associated with hippocampal volume

The hippocampal formation is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stress responsiveness. Structural abnormalities in hippocampal volume and shape are found in several common neuropsychiatric disorders. To identify the genetic underpinnings of hippocampal structure here we perform a genome-wide association study (GWAS) of 33,536 individuals and discover six independent loci significantly associated with hippocampal volume, four of them novel. Of the novel loci, three lie within genes (ASTN2, DPP4 and MAST4) and one is found 200 kb upstream of SHH. A hippocampal subfield analysis shows that a locus within the MSRB3 gene shows evidence of a localized effect along the dentate gyrus, subiculum, CA1 and fissure. Further, we show that genetic variants associated with decreased hippocampal volume are also associated with increased risk for Alzheimer's disease (rg =-0.155). Our findings suggest novel biological pathways through which human genetic variation influences hippocampal volume and risk for neuropsychiatric illness

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Intracranial volume reflects the maximally attained brain size during development, and remains stable with loss of tissue in late life. It is highly heritable, but the underlying genes remain largely undetermined. In a genome-wide association study of 32,438 adults, we discovered five novel loci for intracranial volume and confirmed two known signals. Four of the loci are also associated with adult human stature, but these remained associated with intracranial volume after adjusting for height. We found a high genetic correlation with child head circumference (ρgenetic=0.748), which indicated a similar genetic background and allowed for the identification of four additional loci through meta-analysis (Ncombined = 37,345). Variants for intracranial volume were also related to childhood and adult cognitive function, Parkinson’s disease, and enriched near genes involved in growth pathways including PI3K–AKT signaling. These findings identify biological underpinnings of intracranial volume and provide genetic support for theories on brain reserve and brain overgrowth

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