Practical applications of small-angle neutron scattering.

Recent improvements in beam-line accessibility and technology have led to small-angle neutron scattering (SANS) becoming more frequently applied to materials problems. SANS has been used to study the assembly, dispersion, alignment and mixing of nanoscale condensed matter, as well as to characterise the internal structure of organic thin films, porous structures and inclusions within steel. Using time-resolved SANS, growth mechanisms in materials systems and soft matter phase transitions can also be explored. This review is intended for newcomers to SANS as well as experts. Therefore, the basic knowledge required for its use is first summarised. After this introduction, various examples are given of the types of soft and hard matter that have been studied by SANS. The information that can be extracted from the data is highlighted, alongside the methods used to obtain it. In addition to presenting the findings, explanations are provided on how the SANS measurements were optimised, such as the use of contrast variation to highlight specific parts of a structure. Emphasis is placed on the use of complementary techniques to improve data quality (e.g. using other scattering methods) and the accuracy of data analysis (e.g. using microscopy to separately determine shape and size). This is done with a view to providing guidance on how best to design and analyse future SANS measurements on materials not listed below

Viruses in coral reef ecosystems : implications for nutrient cycling and coral health

Viruses are abundant and ubiquitous across aquatic ecosystems; they infect organisms ranging in size from bacteria to whales, and have important roles in biogeochemical processes. However, one ecosystem where information regarding viral ecology is limited is in coral reefs. Consequently, the main objective of this thesis was to increase our understanding of the presence and roles of viruses in coral reef ecosystems. Virus-like particle (VLP) abundances and distributions were quantified in reef waters, carbonate reef sediments and coral reef micro-habitats, using flow cytometry. In addition, transmission electron microscopy (TEM) was used to determine the presence, and to document the morphologies of VLPs within the coral-surface microlayer (CSM), and within scleractinan coral tissues. VLPs were shown to be abundant members of the coral reef planktonic and benthic microbial community, and were directly and indirectly influenced by the release of coral spawn. VLP abundances in sediments, which exceeded reef water VLP abundances by up to two orders of magnitude, were significantly correlated with bacterial abundances, suggesting bacteria were the dominant hosts for VLPs. Between different coral reef micro-habitats, VLP abundances varied by up to 16-fold, with highest VLP abundances co-occurring with highest bacterial abundances within the coral-surface microlayer (CSM) of Acropora muricata. Viral production rates in the CSM of Favia lizardensis exceeded those in overlying waters by 5-fold, further suggesting strong viral pressure occurs within the CSM micro-habitat. VLPs within the CSM of A. muricata and Porites spp. were morphologically diverse and generally distinct from VLPs within overlying reef water. The similarity of many VLPs to known viruses infecting bacteria, archaea, fungi and microalgae, suggest that a range of potential VLPs hosts occur within the CSM. VLPs were also shown to occur within tissues from A. muricata coral colonies. The most common viral morphotype exhibited icosahedral symmetry and was 120 – 150 nm in diameter. However, other VLP morphotypes were also observed, suggesting that different viruses are infecting different organisms within the coral holobiont, or that one host is susceptible to infection from more than one type of virus. The implications for viral infections in coral reef ecosystems are that viral lysis may alleviate nutrient limitation and contribute to the known high productivity rates that occur in these systems. Furthermore, viral associations with corals are likely to have important implications for coral health. The findings of this thesis provide novel information regarding distributions and potential roles that viruses have in coral reef trophodynamics

Prevalence of virus-like particles within a staghorn scleractinian coral (Acropora muricata) from the Great Barrier Reef

Transmission electron microscopy (TEM) was used to determine whether Acropora muricata coral colonies from the Great Barrier Reef (GBR), Australia, harboured virus-like particles (VLPs). VLPs were present in all coral colonies sampled at Heron Island (southern GBR) and in tagged coral colonies sampled in at least two of the three sampling periods at Lizard Island (northern GBR). VLPs were observed within gastrodermal and epidermal tissues, and on rarer occasions, within the mesoglea. These VLPs had similar morphologies to known prokaryotic and eukaryotic viruses in other systems. Icosahedral VLPs were observed most frequently, however, filamentous VLPs (FVLPs) and phage were also noted. There were no clear differences in VLP size, morphology or location within the tissues with respect to sample date, coral health status or site. The most common VLP morphotype exhibited icosahedral symmetry, 120–150 nm in diameter, with an electron-dense core and an electronlucent membrane. Larger VLPs of similar morphology were also common. VLPs occurred as single entities, in groups, or in dense clusters, either as free particles within coral tissues, or within membrane-bound vacuoles. VLPs were commonly observed within the perinuclear region, with mitochondria, golgi apparatus and crescent-shaped particles frequently observed within close proximity. The host(s) of these observed VLPs was not clear; however, the different sizes and morphologies of VLPs observed within A. muricata tissues suggest that viruses are infecting either the coral animal, zooxanthellae, intracellular bacteria and/or other coral-associated microbiota, or that the one host is susceptible to infection from more than one type of virus. These results add to the limited but emerging body of evidence that viruses represent another potentially important component of the coral holobiont

Spatial dynamics of virus-like particles and heterotrophic bacteria within a shallow coral reef system

Variations in the abundance and community characteristics of virus-like particles (VLP) and heterotrophic bacteria within a shallow, near-shore coral reef were determined using flow cytometric analysis. Mean concentrations of 6.5 x 10(5) and 1.3 x 10(5) Ml(-1) were observed for VLP and bacterioplankton, respectively, although concentrations of both populations varied significantly (p < 0.05) between 4 distinct reef water types. Significant (p < 0.05) variability in the percentage of high DNA (HDNA) bacteria, applied here as an estimate of the proportion of active bacterial cells, and the virus:bacteria ratio (VBR) was also observed between different reef water types. Microscale profiles were taken in the 12 cm layer of water directly above the surface of coral colonies to determine the small-scale spatial relationships between coral colonies and planktonic microbial communities. Across these profiles, mean changes of 2- and 3.5-fold were observed for bacterioplankton and VLP communities, respectively, with VLP abundance positively correlated to bacteria in 75% of profiles. Bacterial and VLP abundance, percentage of HDNA bacteria, and VBR all generally exhibited increasing trends with proximity to the coral surface. VLP abundance was significantly higher (p < 0.05) in the 4 cm closest to the coral surface, and the VBR was higher at the coral surface than in any other zone. The patterns observed here indicate that VLP represent an abundant and dynamic community within coral reefs, are apparently coupled to the spatial dynamics of the bacterioplankton community, and may consequently significantly influence nutrient cycling rates and food-web structure within coral reef ecosystems

Bacterial and viral dynamics during a mass coral spawning period on the Great Barrier Reef

Bacterial and virus-like particle (VLP) abundances and physical and chemical parameters were measured in reef water and sediments over a 10 d period, coinciding with mass coral spawning at Heron Island, Great Barrier Reef. Bacterial abundances in reef water increased 2-fold after spawning and remained elevated for 3 d, before declining to below pre-spawning values. Reef water VLP abundances were also elevated 2 d after spawning; however, VLP abundances exhibited a general decline over the study. Dissolved oxygen (DO) and total nitrogen (TN) concentrations appeared to be dominant factors driving reef water bacterial and VLP dynamics. Sediment bacterial and VLP abundances exceeded those in the water column by up to 3 orders of magnitude and exhibited strong positive correlations for all investigated sediment depths. While short-lived peaks in bacterial and VLP abundances within sediments lagged behind water column trends by 2 d, reef water total phosphorus (TP) concentrations were strongly correlated with sediment bacterial and VLP abundances. Shifts in bacterial and VLP abundances in reef water and sediments during the study corresponded with 2 distinct periods: one prior to, and one after the first night of intense spawning. Scavenging by sedimenting coral spawn material is proposed as a direct mechanism contributing to these shifts, by removing bacteria and VLPs from the water column. The input of organic matter and associated nutrients from mass coral spawning, and the immediate and strongly correlated responses of bacteria and VLPs, indicate that viruses are important players in nutrient cycling processes in coral reefs

Large-scale migration into Britain during the Middle to Late Bronze Age

Present-day people from England and Wales harbour more ancestry derived from Early European Farmers (EEF) than people of the Early Bronze Age . To understand this, we generated genome-wide data from 793 individuals, increasing data from the Middle to Late Bronze and Iron Age in Britain by 12-fold, and Western and Central Europe by 3.5-fold. Between 1000 and 875 BC, EEF ancestry increased in southern Britain (England and Wales) but not northern Britain (Scotland) due to incorporation of migrants who arrived at this time and over previous centuries, and who were genetically most similar to ancient individuals from France. These migrants contributed about half the ancestry of Iron Age people of England and Wales, thereby creating a plausible vector for the spread of early Celtic languages into Britain. These patterns are part of a broader trend of EEF ancestry becoming more similar across central and western Europe in the Middle to Late Bronze Age, coincident with archaeological evidence of intensified cultural exchange . There was comparatively less gene flow from continental Europe during the Iron Age, and Britain's independent genetic trajectory is also reflected in the rise of the allele conferring lactase persistence to ~50% by this time compared to ~7% in central Europe where it rose rapidly in frequency only a millennium later. This suggests that dairy products were used in qualitatively different ways in Britain and in central Europe over this period. [Abstract copyright: © 2021. The Author(s), under exclusive licence to Springer Nature Limited.

Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010

Background Measuring disease and injury burden in populations requires a composite metric that captures both premature mortality and the prevalence and severity of ill-health. The 1990 Global Burden of Disease study proposed disability-adjusted life years (DALYs) to measure disease burden. No comprehensive update of disease burden worldwide incorporating a systematic reassessment of disease and injury-specific epidemiology has been done since the 1990 study. We aimed to calculate disease burden worldwide and for 21 regions for 1990, 2005, and 2010 with methods to enable meaningful comparisons over time. Methods We calculated DALYs as the sum of years of life lost (YLLs) and years lived with disability (YLDs). DALYs were calculated for 291 causes, 20 age groups, both sexes, and for 187 countries, and aggregated to regional and global estimates of disease burden for three points in time with strictly comparable definitions and methods. YLLs were calculated from age-sex-country-time-specific estimates of mortality by cause, with death by standardised lost life expectancy at each age. YLDs were calculated as prevalence of 1160 disabling sequelae, by age, sex, and cause, and weighted by new disability weights for each health state. Neither YLLs nor YLDs were age-weighted or discounted. Uncertainty around cause-specific DALYs was calculated incorporating uncertainty in levels of all-cause mortality, cause-specific mortality, prevalence, and disability weights. Findings Global DALYs remained stable from 1990 (2.503 billion) to 2010 (2.490 billion). Crude DALYs per 1000 decreased by 23% (472 per 1000 to 361 per 1000). An important shift has occurred in DALY composition with the contribution of deaths and disability among children (younger than 5 years of age) declining from 41% of global DALYs in 1990 to 25% in 2010. YLLs typically account for about half of disease burden in more developed regions (high-income Asia Pacific, western Europe, high-income North America, and Australasia), rising to over 80% of DALYs in sub-Saharan Africa. In 1990, 47% of DALYs worldwide were from communicable, maternal, neonatal, and nutritional disorders, 43% from non-communicable diseases, and 10% from injuries. By 2010, this had shifted to 35%, 54%, and 11%, respectively. Ischaemic heart disease was the leading cause of DALYs worldwide in 2010 (up from fourth rank in 1990, increasing by 29%), followed by lower respiratory infections (top rank in 1990; 44% decline in DALYs), stroke (fifth in 1990; 19% increase), diarrhoeal diseases (second in 1990; 51% decrease), and HIV/AIDS (33rd in 1990; 351% increase). Major depressive disorder increased from 15th to 11th rank (37% increase) and road injury from 12th to 10th rank (34% increase). Substantial heterogeneity exists in rankings of leading causes of disease burden among regions. Interpretation Global disease burden has continued to shift away from communicable to non-communicable diseases and from premature death to years lived with disability. In sub-Saharan Africa, however, many communicable, maternal, neonatal, and nutritional disorders remain the dominant causes of disease burden. The rising burden from mental and behavioural disorders, musculoskeletal disorders, and diabetes will impose new challenges on health systems. Regional heterogeneity highlights the importance of understanding local burden of disease and setting goals and targets for the post-2015 agenda taking such patterns into account. Because of improved definitions, methods, and data, these results for 1990 and 2010 supersede all previously published Global Burden of Disease results

Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010:a systematic analysis for the Global Burden of Disease Study 2010

BACKGROUND: Non-fatal health outcomes from diseases and injuries are a crucial consideration in the promotion and monitoring of individual and population health. The Global Burden of Disease (GBD) studies done in 1990 and 2000 have been the only studies to quantify non-fatal health outcomes across an exhaustive set of disorders at the global and regional level. Neither effort quantified uncertainty in prevalence or years lived with disability (YLDs).METHODS: Of the 291 diseases and injuries in the GBD cause list, 289 cause disability. For 1160 sequelae of the 289 diseases and injuries, we undertook a systematic analysis of prevalence, incidence, remission, duration, and excess mortality. Sources included published studies, case notification, population-based cancer registries, other disease registries, antenatal clinic serosurveillance, hospital discharge data, ambulatory care data, household surveys, other surveys, and cohort studies. For most sequelae, we used a Bayesian meta-regression method, DisMod-MR, designed to address key limitations in descriptive epidemiological data, including missing data, inconsistency, and large methodological variation between data sources. For some disorders, we used natural history models, geospatial models, back-calculation models (models calculating incidence from population mortality rates and case fatality), or registration completeness models (models adjusting for incomplete registration with health-system access and other covariates). Disability weights for 220 unique health states were used to capture the severity of health loss. YLDs by cause at age, sex, country, and year levels were adjusted for comorbidity with simulation methods. We included uncertainty estimates at all stages of the analysis.FINDINGS: Global prevalence for all ages combined in 2010 across the 1160 sequelae ranged from fewer than one case per 1 million people to 350,000 cases per 1 million people. Prevalence and severity of health loss were weakly correlated (correlation coefficient -0·37). In 2010, there were 777 million YLDs from all causes, up from 583 million in 1990. The main contributors to global YLDs were mental and behavioural disorders, musculoskeletal disorders, and diabetes or endocrine diseases. The leading specific causes of YLDs were much the same in 2010 as they were in 1990: low back pain, major depressive disorder, iron-deficiency anaemia, neck pain, chronic obstructive pulmonary disease, anxiety disorders, migraine, diabetes, and falls. Age-specific prevalence of YLDs increased with age in all regions and has decreased slightly from 1990 to 2010. Regional patterns of the leading causes of YLDs were more similar compared with years of life lost due to premature mortality. Neglected tropical diseases, HIV/AIDS, tuberculosis, malaria, and anaemia were important causes of YLDs in sub-Saharan Africa.INTERPRETATION: Rates of YLDs per 100,000 people have remained largely constant over time but rise steadily with age. Population growth and ageing have increased YLD numbers and crude rates over the past two decades. Prevalences of the most common causes of YLDs, such as mental and behavioural disorders and musculoskeletal disorders, have not decreased. Health systems will need to address the needs of the rising numbers of individuals with a range of disorders that largely cause disability but not mortality. Quantification of the burden of non-fatal health outcomes will be crucial to understand how well health systems are responding to these challenges. Effective and affordable strategies to deal with this rising burden are an urgent priority for health systems in most parts of the world.FUNDING: Bill &amp; Melinda Gates Foundation.</p

Health-status outcomes with invasive or conservative care in coronary disease

BACKGROUND In the ISCHEMIA trial, an invasive strategy with angiographic assessment and revascularization did not reduce clinical events among patients with stable ischemic heart disease and moderate or severe ischemia. A secondary objective of the trial was to assess angina-related health status among these patients. METHODS We assessed angina-related symptoms, function, and quality of life with the Seattle Angina Questionnaire (SAQ) at randomization, at months 1.5, 3, and 6, and every 6 months thereafter in participants who had been randomly assigned to an invasive treatment strategy (2295 participants) or a conservative strategy (2322). Mixed-effects cumulative probability models within a Bayesian framework were used to estimate differences between the treatment groups. The primary outcome of this health-status analysis was the SAQ summary score (scores range from 0 to 100, with higher scores indicating better health status). All analyses were performed in the overall population and according to baseline angina frequency. RESULTS At baseline, 35% of patients reported having no angina in the previous month. SAQ summary scores increased in both treatment groups, with increases at 3, 12, and 36 months that were 4.1 points (95% credible interval, 3.2 to 5.0), 4.2 points (95% credible interval, 3.3 to 5.1), and 2.9 points (95% credible interval, 2.2 to 3.7) higher with the invasive strategy than with the conservative strategy. Differences were larger among participants who had more frequent angina at baseline (8.5 vs. 0.1 points at 3 months and 5.3 vs. 1.2 points at 36 months among participants with daily or weekly angina as compared with no angina). CONCLUSIONS In the overall trial population with moderate or severe ischemia, which included 35% of participants without angina at baseline, patients randomly assigned to the invasive strategy had greater improvement in angina-related health status than those assigned to the conservative strategy. The modest mean differences favoring the invasive strategy in the overall group reflected minimal differences among asymptomatic patients and larger differences among patients who had had angina at baseline