An oviposition trap to collect immatures of coprophagous moth flies (Diptera: Psychodidae)

Larvae of Psychodidae develop in a variety of breeding sites, including vertebrate feces. As searching for the larvae can be an extremely difficult task, immatures of many species are little known, with descriptions of coprophagous moth flies all from outside the Neotropics. In an attempt to mitigate this challenge, we tested an oviposition trap using cattle dung as attractant, measured the efficiency and specificity of the traps and the most efficient period of exposition in the field. With 60 traps installed in one fragment of ombrophilous forest, 344 immatures were collected, distributed in four species of Psychoda and one of Feuerborniella. Psychodidae accounted for 75% of the collected Diptera. The high specificity of the trap to Psychodidae contrasts with other studies on coprophagous fauna where they appear in low abundance. Based on the metrics in this study, the most efficient period of trapping exposition was between five to eight days, but the difference was not significant probably due to the high number of zero observations among the traps. Many questions pertaining to coprophagous moth flies remain unanswered. Further research is needed to improve trapping efficiency, elucidate the effects of attractants and determine how environmental factors influence the attractiveness of bait

Presença e alterações da fauna de Artrópodos durante a preparação de um composto orgânico

During the preparation oforganic, compost (150 days) five samples were taken of the arthropod fauna in each of three diferent treatments: fresh vegetable material alone (treatment 1); treatment 1 with chicken manure (treatment 2); and treatment 1 with residues of barley (treatment 3). All treatments were inoculated with bacteria after 75 days and all were covered by plastic sheetting for the greater part of the study period. In all of the three treatments, the most numerically important group was the Acari (88-99,5%) fallowed by Collembola (03-01%), Colleoptera (0,1-1,4%), Diplopoda (0,04-0,31%), Diptera (0,4-0,65%), and Formicidae. (0,01 -0,03%). The number individuals, and taxonomic groups, of the fauna increased gradually during the preparation of the compost, in all treatments. The bacterial inoculation at 75 days, produced an increase in the fauna in treatments I and 3, but not in treatment 2, moot likely because the chicken manure already had suffient microorganisms to ensure maximum degradation of the vegetable material. Covering the compost, heaps with plastic clearly decreased the number of arthropods. Uncovered compost treated with chicken manure has the highest taxonomic diversity of arthropods and the fastest rate of decomposition.No decorrer da preparação de um composto orgânico (150 dias de duração), foram feitas cinco amostragens para estudarem-se a presença e as alterações da fauna de artrópodos, durante algumas das diferentes fases de sua preparação. Foram utilizados, em seis canteiros feitos acima da superfície do solo, três tratamentos diferentes, além da inoculação bacteriana de três dos canteiros, aos 75 dias, e da cobertura de todos os canteiros com plástico durante uma boa parte do tempo de preparação do composto. Em todos os tratamentos, o grupo numericamente mais importante foi Acari (88-99, 5%), seguido por Collembola (0,3- 0%), Coleoptera (0, 1-1, 4%), Diplopoda (0,04-0,3%), Diptera (0,04-0,65%) e Formicidae (0,01-0,03%). O número de grupos taxonômicos e de indivíduos da fauna aumentou gradativamente com o tempo de preparação do composto, em todas os tratamentos. A inoculação bacteriana, aos 75 dias, resultou num incremento da fauna no tratamento 2 (com esterco de galinha), provavelmente em face do anterior fornecimento de uma eficiente fonte de nitrogênio e de microorganismos, representada pela adição inicial de esterco de galinha fresca ao material vegetal. Também a cobertura dos canteiros com plástico parece ter influido bastante na fauna presente no material, provocando uma sensível diminuição de sua densidade. O tratamento com esterco de galinha foi o que apresentou uma mais rápida colonização pela fauna, com uma maior diversidade de grupos taxonômicos e também o que teve uma mais rápida e completa humificação do material

Efficiency in inventories of ants in a forest reserve in Central Amazonia

O objetivo deste trabalho foi avaliar a eficiência da metodologia de inventário de formigas. Foram usadas subamostras coletadas em 24 transectos de 100 m, distribuídos em 6 parcelas de 600 ha, em floresta primária, como parte de um projeto de longa duração. Dez subamostras foram extraídas por transecto com extratores de Winkler. As formigas foram identificadas quanto ao gênero. Crematogaster, Gnamptogenys e Pachycondyla foram identificados quanto a espécies ou morfoespécies. Para avaliar as consequências de redução da amostragem na retenção da informação ecológica, foi estimado o menor número de subamostras necessário para detectar os efeitos das variáveis ambientais. A ordenação em escala multidimencionais (MDS) foi usada para gerar matrizes de dissimilaridade, e as correlações de Mantel, entre cada esforço reduzido de amostragem e o esforço máximo, foram usadas como índice da informação retida que ainda poderia ser usada em análises multivariadas. Foram detectados baixos valores de probabilidade para os efeitos do pH do solo na comunidade de gêneros e do efeito do volume de serapilheira na comunidade de Crematogaster. O mesmo padrão foi detectado em análises baseadas em amostragem reduzida. O número de subamostras pode ser reduzido e o custo-benefício do protocolo otimizado, com pouca perda de informação.The objective of this work was to evaluate an inventory method efficiency for ants. We used subsamples collected in 24 transects of 100 m, distributed in 6 plots of 600 ha each in primary forest, as part of a long-term project. Ten litter subsamples were extracted per transect using Winkler extractors. Ants were identified to genus level, and Crematogaster, Gnamptogenys and Pachycondyla genera to species/morphospecies level. To evaluate the consequences of reduced sampling on the retention of ecological information, we estimated the lowest number of subsamples needed to detect the effects of environmental variables. Multidimensional scaling (MDS) was used to generate dissimilarity matrices, and Mantel correlations between each reduced-sampling effort and maximum effort were used as an index of how much information was maintained and could still be used in multivariate analyses. Lower p-values was observed on the effect of soil pH in the community of genera, and on the effect of the litter volume for the community of Crematogaster. The trend was still detectable in the analysis based on reduced-sampling. The number of subsamples can be reduced, and the cost-efficiency of the protocol can be improved with little loss of information

The resistance to submersion of terrestrial Acari (Acari: Oribatida) from flooded and non-flooded forests of Central Amazonia in experimental laboratorial conditions

Specimens of Rostrozetes foveolatus were obtained from two inundated forest areas várzea" and "igapó") and from two nonflooded secondary forests in the Central Amazon Region. The survival rates of their populations under submerged and nonsubmerged conditions were compared in laboratory conditions. The "igapó" population was sampled during three periods in 1992: before (February: litter nonsubmerged), in the beginning (April: litter submerged) and in the peak of the inundation phase (July: litter submerged). At "igapó", the animals survived better when submitted to nonsubmerged conditions, meaning that submersion is a stress factor. The same result did not occur at "várzea", signifying a better adaptation of this population to the submersion stress. The lowest flood resistance (27 days) was found in animals from "terra firme" secondary forest, away from the igapó. A considerable submersion resistance in the population sampled in the secondary forest, near the igapó forest, was comparable to the populations of the inundated areas and greater than the resistence at "terra-firme", far away from the "igapó". Animals sampled in February of 1996 (reared individually in plastic containers), from the flooded forests had significantly higher survival rates than those from secondary forests. Three situations in relation to the submersion period were registered: a) one of "várzea", with a more resistant population, b) one of "igapó", with a intermediate resistance and c) one of "terra-firme", away from the "igapó", with a lower resistant population. In twelve of the fifteen species studied, a high resistance to submersion was also registered.Espécimens de Rostrozetes foveolatus foram obtidos de duas florestas inundáveis (várzea e igapó) e de duas florestas secundárias (terra firme) da Amazônia Central. As populações foram comparadas para a obtenção da taxa de sobrevivência em experimentos de laboratório nas condições submersas e não submersas. As coletas no igapó foram efetuadas em três períodos de 1992antes (fevereiroserapilheira não submersa), no início (abrilserapilheira submersa) e no pico da inundação (julhoserapilheira submersa). No igapó, os animais sobreviveram melhor em condição não submersa, significando que a submersão é um fator de estresse. O mesmo não ocorreu na várzea, indicando que esta população está melhor adaptada ao estresse da submersão. A menor resistência à submersão (27 dias) foi registrada nos animais de uma floresta secundária da terra firme, situada longe do igapó. Na população da terra firme próxima ao igapó, a resistência a submersão foi comparável à registrada para as populações das áreas inundáveis e maior do que a registrada em terra firme longe do igapó. Em experimentos com animais coletados em fevereiro de 1996 (mantidos individualmente em recipientes plásticos), as populações das florestas inundáveis tiveram taxa de sobrevivência significativamente maior em relação aos das florestas não inundáveis. Três situações foram registradas quanto a resistência à submersãoa) a da várzea, com população mais resistente, b) a do igapó, com uma população intermediária e c) a da terra-firme longe do igapó, com uma população menos resistente. Em doze das outras quinze espécies estudadas foi registrada alta resistência às condições de submersão

Pervasive gaps in Amazonian ecological research

Biodiversity loss is one of the main challenges of our time,1,2 and attempts to address it require a clear un derstanding of how ecological communities respond to environmental change across time and space.3,4 While the increasing availability of global databases on ecological communities has advanced our knowledge of biodiversity sensitivity to environmental changes,5–7 vast areas of the tropics remain understudied.8–11 In the American tropics, Amazonia stands out as the world’s most diverse rainforest and the primary source of Neotropical biodiversity,12 but it remains among the least known forests in America and is often underrepre sented in biodiversity databases.13–15 To worsen this situation, human-induced modifications16,17 may elim inate pieces of the Amazon’s biodiversity puzzle before we can use them to understand how ecological com munities are responding. To increase generalization and applicability of biodiversity knowledge,18,19 it is thus crucial to reduce biases in ecological research, particularly in regions projected to face the most pronounced environmental changes. We integrate ecological community metadata of 7,694 sampling sites for multiple or ganism groups in a machine learning model framework to map the research probability across the Brazilian Amazonia, while identifying the region’s vulnerability to environmental change. 15%–18% of the most ne glected areas in ecological research are expected to experience severe climate or land use changes by 2050. This means that unless we take immediate action, we will not be able to establish their current status, much less monitor how it is changing and what is being lostinfo:eu-repo/semantics/publishedVersio

Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019

Background: In an era of shifting global agendas and expanded emphasis on non-communicable diseases and injuries along with communicable diseases, sound evidence on trends by cause at the national level is essential. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) provides a systematic scientific assessment of published, publicly available, and contributed data on incidence, prevalence, and mortality for a mutually exclusive and collectively exhaustive list of diseases and injuries. Methods: GBD estimates incidence, prevalence, mortality, years of life lost (YLLs), years lived with disability (YLDs), and disability-adjusted life-years (DALYs) due to 369 diseases and injuries, for two sexes, and for 204 countries and territories. Input data were extracted from censuses, household surveys, civil registration and vital statistics, disease registries, health service use, air pollution monitors, satellite imaging, disease notifications, and other sources. Cause-specific death rates and cause fractions were calculated using the Cause of Death Ensemble model and spatiotemporal Gaussian process regression. Cause-specific deaths were adjusted to match the total all-cause deaths calculated as part of the GBD population, fertility, and mortality estimates. Deaths were multiplied by standard life expectancy at each age to calculate YLLs. A Bayesian meta-regression modelling tool, DisMod-MR 2.1, was used to ensure consistency between incidence, prevalence, remission, excess mortality, and cause-specific mortality for most causes. Prevalence estimates were multiplied by disability weights for mutually exclusive sequelae of diseases and injuries to calculate YLDs. We considered results in the context of the Socio-demographic Index (SDI), a composite indicator of income per capita, years of schooling, and fertility rate in females younger than 25 years. Uncertainty intervals (UIs) were generated for every metric using the 25th and 975th ordered 1000 draw values of the posterior distribution. Findings: Global health has steadily improved over the past 30 years as measured by age-standardised DALY rates. After taking into account population growth and ageing, the absolute number of DALYs has remained stable. Since 2010, the pace of decline in global age-standardised DALY rates has accelerated in age groups younger than 50 years compared with the 1990–2010 time period, with the greatest annualised rate of decline occurring in the 0–9-year age group. Six infectious diseases were among the top ten causes of DALYs in children younger than 10 years in 2019: lower respiratory infections (ranked second), diarrhoeal diseases (third), malaria (fifth), meningitis (sixth), whooping cough (ninth), and sexually transmitted infections (which, in this age group, is fully accounted for by congenital syphilis; ranked tenth). In adolescents aged 10–24 years, three injury causes were among the top causes of DALYs: road injuries (ranked first), self-harm (third), and interpersonal violence (fifth). Five of the causes that were in the top ten for ages 10–24 years were also in the top ten in the 25–49-year age group: road injuries (ranked first), HIV/AIDS (second), low back pain (fourth), headache disorders (fifth), and depressive disorders (sixth). In 2019, ischaemic heart disease and stroke were the top-ranked causes of DALYs in both the 50–74-year and 75-years-and-older age groups. Since 1990, there has been a marked shift towards a greater proportion of burden due to YLDs from non-communicable diseases and injuries. In 2019, there were 11 countries where non-communicable disease and injury YLDs constituted more than half of all disease burden. Decreases in age-standardised DALY rates have accelerated over the past decade in countries at the lower end of the SDI range, while improvements have started to stagnate or even reverse in countries with higher SDI. Interpretation: As disability becomes an increasingly large component of disease burden and a larger component of health expenditure, greater research and developm nt investment is needed to identify new, more effective intervention strategies. With a rapidly ageing global population, the demands on health services to deal with disabling outcomes, which increase with age, will require policy makers to anticipate these changes. The mix of universal and more geographically specific influences on health reinforces the need for regular reporting on population health in detail and by underlying cause to help decision makers to identify success stories of disease control to emulate, as well as opportunities to improve. Funding: Bill & Melinda Gates Foundation. © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 licens

Outcomes from elective colorectal cancer surgery during the SARS-CoV-2 pandemic

This study aimed to describe the change in surgical practice and the impact of SARS-CoV-2 on mortality after surgical resection of colorectal cancer during the initial phases of the SARS-CoV-2 pandemic

Global, regional, and national under-5 mortality, adult mortality, age-specific mortality, and life expectancy, 1970–2016: a systematic analysis for the Global Burden of Disease Study 2016

BACKGROUND: Detailed assessments of mortality patterns, particularly age-specific mortality, represent a crucial input that enables health systems to target interventions to specific populations. Understanding how all-cause mortality has changed with respect to development status can identify exemplars for best practice. To accomplish this, the Global Burden of Diseases, Injuries, and Risk Factors Study 2016 (GBD 2016) estimated age-specific and sex-specific all-cause mortality between 1970 and 2016 for 195 countries and territories and at the subnational level for the five countries with a population greater than 200 million in 2016. METHODS: We have evaluated how well civil registration systems captured deaths using a set of demographic methods called death distribution methods for adults and from consideration of survey and census data for children younger than 5 years. We generated an overall assessment of completeness of registration of deaths by dividing registered deaths in each location-year by our estimate of all-age deaths generated from our overall estimation process. For 163 locations, including subnational units in countries with a population greater than 200 million with complete vital registration (VR) systems, our estimates were largely driven by the observed data, with corrections for small fluctuations in numbers and estimation for recent years where there were lags in data reporting (lags were variable by location, generally between 1 year and 6 years). For other locations, we took advantage of different data sources available to measure under-5 mortality rates (U5MR) using complete birth histories, summary birth histories, and incomplete VR with adjustments; we measured adult mortality rate (the probability of death in individuals aged 15-60 years) using adjusted incomplete VR, sibling histories, and household death recall. We used the U5MR and adult mortality rate, together with crude death rate due to HIV in the GBD model life table system, to estimate age-specific and sex-specific death rates for each location-year. Using various international databases, we identified fatal discontinuities, which we defined as increases in the death rate of more than one death per million, resulting from conflict and terrorism, natural disasters, major transport or technological accidents, and a subset of epidemic infectious diseases; these were added to estimates in the relevant years. In 47 countries with an identified peak adult prevalence for HIV/AIDS of more than 0·5% and where VR systems were less than 65% complete, we informed our estimates of age-sex-specific mortality using the Estimation and Projection Package (EPP)-Spectrum model fitted to national HIV/AIDS prevalence surveys and antenatal clinic serosurveillance systems. We estimated stillbirths, early neonatal, late neonatal, and childhood mortality using both survey and VR data in spatiotemporal Gaussian process regression models. We estimated abridged life tables for all location-years using age-specific death rates. We grouped locations into development quintiles based on the Socio-demographic Index (SDI) and analysed mortality trends by quintile. Using spline regression, we estimated the expected mortality rate for each age-sex group as a function of SDI. We identified countries with higher life expectancy than expected by comparing observed life expectancy to anticipated life expectancy on the basis of development status alone. FINDINGS: Completeness in the registration of deaths increased from 28% in 1970 to a peak of 45% in 2013; completeness was lower after 2013 because of lags in reporting. Total deaths in children younger than 5 years decreased from 1970 to 2016, and slower decreases occurred at ages 5-24 years. By contrast, numbers of adult deaths increased in each 5-year age bracket above the age of 25 years. The distribution of annualised rates of change in age-specific mortality rate differed over the period 2000 to 2016 compared with earlier decades: increasing annualised rates of change were less frequent, although rising annualised rates of change still occurred in some locations, particularly for adolescent and younger adult age groups. Rates of stillbirths and under-5 mortality both decreased globally from 1970. Evidence for global convergence of death rates was mixed; although the absolute difference between age-standardised death rates narrowed between countries at the lowest and highest levels of SDI, the ratio of these death rates-a measure of relative inequality-increased slightly. There was a strong shift between 1970 and 2016 toward higher life expectancy, most noticeably at higher levels of SDI. Among countries with populations greater than 1 million in 2016, life expectancy at birth was highest for women in Japan, at 86·9 years (95% UI 86·7-87·2), and for men in Singapore, at 81·3 years (78·8-83·7) in 2016. Male life expectancy was generally lower than female life expectancy between 1970 and 2016, an