20 research outputs found

    List of species of spiders (Arachnida, Araneae) from the Pico da Neblina, state of Amazonas, Brazil

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    We present a list of species of spiders collected at the Pico da Neblina, the highest mountain in Brazil (Amazonas, Brazil). We sampled at six altitudes (100, 400, 860, 1,550, 2,000 and 2,400 m a.s.l.), through manual active search, during the night and with a beating tray, during the day. We obtained a total of 3,143 adult individuals, which were assigned to 529 species, from 39 families. The most species rich families were Theridiidae (108 species), Araneidae (98 species) and Salticidae (60 species). Most species were rarely collected, as 389 (73% of total richness) species were represented by up to five individuals, and 197 (37% of total richness) of them by just one individual. We briefly compare our results with those from other spider surveys in the Amazon basin

    Land use and soil characteristics affect soil organisms differently from above-ground assemblages

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    Background: Land-use is a major driver of changes in biodiversity worldwide, but studies have overwhelmingly focused on above-ground taxa: the effects on soil biodiversity are less well known, despite the importance of soil organisms in ecosystem functioning. We modelled data from a global biodiversity database to compare how the abundance of soil-dwelling and above-ground organisms responded to land use and soil properties. Results: We found that land use affects overall abundance differently in soil and above-ground assemblages. The abundance of soil organisms was markedly lower in cropland and plantation habitats than in primary vegetation and pasture. Soil properties influenced the abundance of soil biota in ways that differed among land uses, suggesting they shape both abundance and its response to land use. Conclusions: Our results caution against assuming models or indicators derived from above-ground data can apply to soil assemblages and highlight the potential value of incorporating soil properties into biodiversity models.Natural Environment Research Council (NERC): NE/L002515/1 and NE/M014533/1. European Union funding: 81794

    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

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    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

    Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950-2019 : a comprehensive demographic analysis for the Global Burden of Disease Study 2019

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    Background: Accurate and up-to-date assessment of demographic metrics is crucial for understanding a wide range of social, economic, and public health issues that affect populations worldwide. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2019 produced updated and comprehensive demographic assessments of the key indicators of fertility, mortality, migration, and population for 204 countries and territories and selected subnational locations from 1950 to 2019. Methods: 8078 country-years of vital registration and sample registration data, 938 surveys, 349 censuses, and 238 other sources were identified and used to estimate age-specific fertility. Spatiotemporal Gaussian process regression (ST-GPR) was used to generate age-specific fertility rates for 5-year age groups between ages 15 and 49 years. With extensions to age groups 10–14 and 50–54 years, the total fertility rate (TFR) was then aggregated using the estimated age-specific fertility between ages 10 and 54 years. 7417 sources were used for under-5 mortality estimation and 7355 for adult mortality. ST-GPR was used to synthesise data sources after correction for known biases. Adult mortality was measured as the probability of death between ages 15 and 60 years based on vital registration, sample registration, and sibling histories, and was also estimated using ST-GPR. HIV-free life tables were then estimated using estimates of under-5 and adult mortality rates using a relational model life table system created for GBD, which closely tracks observed age-specific mortality rates from complete vital registration when available. Independent estimates of HIV-specific mortality generated by an epidemiological analysis of HIV prevalence surveys and antenatal clinic serosurveillance and other sources were incorporated into the estimates in countries with large epidemics. Annual and single-year age estimates of net migration and population for each country and territory were generated using a Bayesian hierarchical cohort component model that analysed estimated age-specific fertility and mortality rates along with 1250 censuses and 747 population registry years. We classified location-years into seven categories on the basis of the natural rate of increase in population (calculated by subtracting the crude death rate from the crude birth rate) and the net migration rate. We computed healthy life expectancy (HALE) using years lived with disability (YLDs) per capita, life tables, and standard demographic methods. Uncertainty was propagated throughout the demographic estimation process, including fertility, mortality, and population, with 1000 draw-level estimates produced for each metric. Findings: The global TFR decreased from 2·72 (95% uncertainty interval [UI] 2·66–2·79) in 2000 to 2·31 (2·17–2·46) in 2019. Global annual livebirths increased from 134·5 million (131·5–137·8) in 2000 to a peak of 139·6 million (133·0–146·9) in 2016. Global livebirths then declined to 135·3 million (127·2–144·1) in 2019. Of the 204 countries and territories included in this study, in 2019, 102 had a TFR lower than 2·1, which is considered a good approximation of replacement-level fertility. All countries in sub-Saharan Africa had TFRs above replacement level in 2019 and accounted for 27·1% (95% UI 26·4–27·8) of global livebirths. Global life expectancy at birth increased from 67·2 years (95% UI 66·8–67·6) in 2000 to 73·5 years (72·8–74·3) in 2019. The total number of deaths increased from 50·7 million (49·5–51·9) in 2000 to 56·5 million (53·7–59·2) in 2019. Under-5 deaths declined from 9·6 million (9·1–10·3) in 2000 to 5·0 million (4·3–6·0) in 2019. Global population increased by 25·7%, from 6·2 billion (6·0–6·3) in 2000 to 7·7 billion (7·5–8·0) in 2019. In 2019, 34 countries had negative natural rates of increase; in 17 of these, the population declined because immigration was not sufficient to counteract the negative rate of decline. Globally, HALE increased from 58·6 years (56·1–60·8) in 2000 to 63·5 years (60·8–66·1) in 2019. HALE increased in 202 of 204 countries and territories between 2000 and 2019

    A revision of the Neotropical genus Austrohahnia Mello-Leitão (Araneae, Hahniidae)

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    The Neotropical genus Austrohahnia Mello-Leitão, 1942 is revised, comprising four species from Argentina. The genus is here transferred to the subfamily Hahniinae Bertkau, 1878 from Cybaeolinae Lehtinen, 1967. Austrohahnia is diagnosed by a single synapomorphy, short setae ventrally on the abdomen, in immature as well as adult stages. The type species A. praestans Mello-Leitão, 1942 is redescribed. Austrohahnia catleyi new species is described and illustrated based both sexes from the alder forests of northwestern Argentina. Austrohahnia melloleitaoi (Schiapelli & Gerschman, 1942) new combination was transferred from Hahnia C.L. Koch, 1841, the male is described and illustrated for the first time, and the female is redescribed. Austrohahnia isophthalma (Mello-Leitão, 1941) new combination is also transferred from Hahnia and considered a nomen dubium. New geographic records of studied species are provided.Fil: Rubio, Gonzalo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Instituto de Biología Subtropical. Instituto de Biología Subtropical - Nodo Puerto Iguazu | Universidad Nacional de Misiones. Instituto de Biología Subtropical. Instituto de Biología Subtropical - Nodo Puerto Iguazu; ArgentinaFil: Lo-Man-Hung, Nancy França. Carste Consultores Associados Ltda; BrasilFil: Iuri, Hernán. División Aracnología. Museo Argentino de Ciencias Naturales “Bernardino Rivadavia”; Argentin

    First record of an onychophoran (Onychophora, Peripatidae) feeding on a theraphosid spider (Araneae, Theraphosidae)

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    Volume: 37Start Page: 116End Page: 11

    The value of primary, secondary, and plantation forests for Neotropical epigeic arachnids.

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    Plantations and secondary forests are becoming dominant components of many tropical forest landscapes. Yet we have an insufficient understanding of the value of these habitats for biodiversity conservation, and almost none for most anthropods in species-rich tropical forests. We sampled epigeie arachnids (Amblypygi, Araneae, Opiliones, Scorpiones, and Uropygi) in primary, secondary (14-19 years), and Eucalyptus plantation (4-5 years) forests in the Jari region of northeastern Brazilian Amazonia. We sampled five independent sites in each forest type between January and June 2005, collecting a total of 4824 individuals (31777 adults, 112 species), including 1864 adults (75 species) in Eucalyptus, 776 (60) in secondary forest, and 536 (72) in primary forest. We compared species richness, species-abundance distributions, and community structure, between the three forest types and identified the species that were characteristic of each forest type. Rarefaction analyses showed that undisturbed primary forest harbored significantly more species and a similar overall abundance as second-growth forest: while levels of species richness were similar between secondary forest and Eucalyptus. The species composition and abundance structure of arachnid assemblages was distinct in all three forest types. Considering all species sampled. 19% were only sampled in primary forest, 4% in secondary forest, and 19% in Eucalyptus. Most species sampled in plantation forests are known to be wide-randing habitat generalists. Our data indicate that regenerating forests are not biological deserts (57% and 56% of species sampled in primary forest were also captured in secondary and plantation forests respectively) and can, therefore, help mitigate some of the negative effects of deforestation for epigeic arachnids. However, these replacement habitats do not provide a substitute for primary forest and may fail to conserve many of those species most at risk from extinction

    Aranhas, escorpiões, opiliões e outros

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    A classe Arachnida é um grupo megadiverso (cerca de 95.000 espécies reconhecidas), amplamente distribuído e muito bem-sucedido nos mais diversos habitats. Essa classe é composta por 11 ordens, todas representadas na região amazônica (SHULTZ, 1990). Dentre elas, os representantes mais conhecidos são as aranhas, escorpiões, carrapatos e ácaros, principalmente por causarem doenças e acidentes a seres humanos e outros animais. É um grupo ainda pouco estudado na Amazônia (BRESCOVIT et al., 2002; BONALDO et al., 2009), o que contribui para que muitas ordens tenham sua diversidade subestimada (ADIS, 2002; KURY, 2003; TOURINHO e PÉREZ, 2006; BONALDO et al., 2009). Por exemplo, para a reserva Ducke, localizada em Manaus, no estado do Amazonas, que tem sido muito bem estudada para todos os grupos de animais através de inventários estruturados, foram registradas 36 espécies de opiliões, sendo que pelo menos 15 ainda não haviam sido descritas pela ciência (PORTO, 2013). Entretanto, atualmente, já sabemos que a diversidade de aracnídeos na Amazônia é alta e comparável à da mata Atlântica, para certas ordens (BONALDO et al., 2009).Fil: Tourinho, Ana Lucia. Ministério da Ciência, Tecnologia, Inovações. Instituto Nacional de Pesquisas da Amazônia; BrasilFil: Lo Man Hung, Nancy França. No especifíca;Fil: Salvatierra, Lidianne. Ministério da Ciência, Tecnologia, Inovações. Instituto Nacional de Pesquisas da Amazônia; BrasilFil: Colmenares, Pio Antonio. Ministério da Ciência, Tecnologia, Inovações. Instituto Nacional de Pesquisas da Amazônia; BrasilFil: Lourenco Porto, Willians. Ministério da Ciência, Tecnologia, Inovações. Instituto Nacional de Pesquisas da Amazônia; Brasil. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Museo Argentino de Ciencias Naturales "Bernardino Rivadavia"; Argentin
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