Efeitos dos excessos de alumínio, cloro e manganês em dois cultivares de soja (Glycine max (L.) Merrill)

Two soybean cultivars, Santa Rosa and FV-1, were grown in nutrient solution in the presence of high concentrations of Al (24 ppm), CI (1750 ppm) and Mn (25 ppm). Observations, measurements and chemical analyses allowed for the following conclusions to be drawn: (1) symptoms of toxicity are in agreement with those described in the literatura; (2) the detrimental effect obeyed the decreasing order - Mn Al CI; (3) dry matter production by the variety UFV - 1 was relatively more affected by the treatments; (4) leaf analyses do not provide a reliable indication of the sensitivity of the two varieties to the high levels of the three elements in the substrate; (5) Ca/Al ratio in the roots keeps a good relationship with the relative tolerance of the two cultivas to excess Al in the medium.Dois cultivares de soja, Santa Rosa e UFV-1, foram cultivados em solução nutritiva na presença de excesso de alumínio, cloro e manganês. Além de provocar o aparecimento de sintomas foliares (cloro e manganês) ou radiculares (alumínio), os elementos em excesso causaram diminuições no crescimento e impediram a produção de vagens. A análise mineral das folhas mostrou a influência dos tratamentos na composição do tecido

Search for the Standard Model Higgs boson decaying into bb¯ produced in association with top quarks decaying hadronically in pp collisions at √s = 8 TeV with the ATLAS detector

A search for Higgs boson production in association with a pair of top quarks (tt¯ H) is performed, where the Higgs boson decays to bb¯, and both top quarks decay hadronically. The data used correspond to an integrated luminosity of 20.3 fb−1 of pp collisions at √s = 8 TeV collected with the ATLAS detector at the Large Hadron Collider. The search selects events with at least six energetic jets and uses a boosted decision tree algorithm to discriminate between signal and Standard Model background. The dominant multijet background is estimated using a dedicated data-driven technique. For a Higgs boson mass of 125 GeV, an upper limit of 6.4 (5.4) times the Standard Model cross section is observed (expected) at 95% confidence level. The best-fit value for the signal strength is μ = 1.6 ± 2.6 times the Standard Model expectation for mH = 125 GeV. Combining all tt¯ H searches carried out by ATLAS at √s = 8 and 7 TeV, an observed (expected) upper limit of 3.1 (1.4) times the Standard Model expectation is obtained at 95% confidence level, with a signal strength μ = 1.7 ± 0.8

Search for the Higgs boson produced in association with a W boson and decaying to four b-quarks via two spin-zero particles in pp collisions at 13 TeV with the ATLAS detector

This paper presents a dedicated search for exotic decays of the Higgs boson to a pair of new spin-zero particles, H → aa, where the particle a decays to b-quarks and has a mass in the range of 20–60 GeV. The search is performed in events where the Higgs boson is produced in association with a W boson, giving rise to a signature of a lepton (electron or muon), missing transverse momentum, and multiple jets from b-quark decays. The analysis is based on the full dataset of pp collisions at √s = 13 TeV recorded in 2015 by the ATLAS detector at the CERN Large Hadron Collider, corresponding to an integrated luminosity of 3.2 fb−1. No significant excess of events above the Standard Model prediction is observed, and a 95% confidence-level upper limit is derived for the product of the production cross section for pp → W H times the branching ratio for the decay H → aa → 4b. The upper limit ranges from 6.2 pb for an a-boson mass ma = 20 GeV to 1.5 pb for ma = 60 GeV

Acúmulo e repartição da matéria seca da planta de pepino tipo conserva sob três doses de nutrientes minerais Dry matter accumulation and distribution of pickling cucumber plants under three mineral nutrient levels

Determinou-se o efeito de três doses de nutrientes minerais sobre o acúmulo e distribuição da matéria seca da planta de pepino tipo conserva, híbrido Crispina. As plantas foram cultivadas em sacolas plásticas com 4,6kg de substrato composto por uma mistura de 40% de casca de arroz e 60% de solo, no interior de uma estufa de polietileno, na primavera de 1998 e no verão de 1999. Foi empregado um delineamento experimental de blocos casualizados, com três repetições e 15 plantas por parcela. Os tratamentos foram constituídos por três níveis múltiplos de uma dose padrão de nutrientes aplicada para cada planta, contendo N-P-K-Ca e Mg nas quantidades de 0,8-0,12-0,8-0,46-0,086g.pl-1, com 0,33m<IMG SRC="http:/img/revistas/cr/v31n3/a04img01.gif"> de solução de micronutrientes e 0,07m<IMG SRC="http:/img/revistas/cr/v31n3/a04img01.gif"> de quelato de ferro. Os níveis corresponderam às quantidades de 50%, 100% e 150% da dose padrão, denominados de tratamentos T1, T2 e T3, respectivamente, aplicados semanalmente através da fertirrigação em todas as plantas de uma mesma parcela. Determinou-se a matéria seca dos diferentes órgãos da parte aérea da planta a intervalos semanais. Houve efeito significativo dos tratamentos no acúmulo da matéria seca, nos dois experimentos. A maior fração foi alocada para os frutos, atingindo o valor mais elevado de 0,64 na primavera. Concluiu-se que a distribuição da matéria seca desse material vegetal não é constante, sofrendo interações com as variáveis do ambiente.<br>It was determined the effect of three mineral nutrient levels on dry matter accumulation and distribution of pickling cucumber plants, hybrid Crispina, grown inside a polyethylene greenhouse, in spring 1998 and in summer 1999. Planting was made in bags filled with 4.6kg of a substrate mixture composed by 40% rice husks and 60% soil. A randomized block experimental design was used, with three replications and15 plants per plot. A reference nutrient dose was supplied weekly to each one of the plants, with the following composition, in g.plant-1 : 0.8 N, 0.12 P, 0.8 K, 0.46 Ca, 0.086 Mg, 0.33m<IMG SRC="http:/img/revistas/cr/v31n3/a04img01.gif"> of a micronutrients mixture and 0.07m<IMG SRC="http:/img/revistas/cr/v31n3/a04img01.gif"> of an iron chelate. Treatments consisted of three levels of the reference nutrient dose, in the proportion of 50%, 100% and 150%, named treatments T1, T2 and T3, respectivelly, applied to plants weekly by fertigation. Dry matter of aerial organs was measured weekly. It was observed a significant effect of nutrition levels on dry matter accumulation, in both experiments. The higher fraction allocated to fruits was 0.64, in the first experiment. It was concluded that dry matter distribution on this material is not constant, due to interactions with environmental variables

Efeitos dos excessos de alumínio, cloro e manganês em dois cultivares de soja (Glycine max (L.) Merrill)

Dois cultivares de soja, Santa Rosa e UFV-1, foram cultivados em solução nutritiva na presença de excesso de alumínio, cloro e manganês. Além de provocar o aparecimento de sintomas foliares (cloro e manganês) ou radiculares (alumínio), os elementos em excesso causaram diminuições no crescimento e impediram a produção de vagens. A análise mineral das folhas mostrou a influência dos tratamentos na composição do tecido.Two soybean cultivars, Santa Rosa and FV-1, were grown in nutrient solution in the presence of high concentrations of Al (24 ppm), CI (1750 ppm) and Mn (25 ppm). Observations, measurements and chemical analyses allowed for the following conclusions to be drawn: (1) symptoms of toxicity are in agreement with those described in the literatura; (2) the detrimental effect obeyed the decreasing order - Mn Al CI; (3) dry matter production by the variety UFV - 1 was relatively more affected by the treatments; (4) leaf analyses do not provide a reliable indication of the sensitivity of the two varieties to the high levels of the three elements in the substrate; (5) Ca/Al ratio in the roots keeps a good relationship with the relative tolerance of the two cultivas to excess Al in the medium

Immunocompromised patients with acute respiratory distress syndrome : Secondary analysis of the LUNG SAFE database

The aim of this study was to describe data on epidemiology, ventilatory management, and outcome of acute respiratory distress syndrome (ARDS) in immunocompromised patients. Methods: We performed a post hoc analysis on the cohort of immunocompromised patients enrolled in the Large Observational Study to Understand the Global Impact of Severe Acute Respiratory Failure (LUNG SAFE) study. The LUNG SAFE study was an international, prospective study including hypoxemic patients in 459 ICUs from 50 countries across 5 continents. Results: Of 2813 patients with ARDS, 584 (20.8%) were immunocompromised, 38.9% of whom had an unspecified cause. Pneumonia, nonpulmonary sepsis, and noncardiogenic shock were their most common risk factors for ARDS. Hospital mortality was higher in immunocompromised than in immunocompetent patients (52.4% vs 36.2%; p < 0.0001), despite similar severity of ARDS. Decisions regarding limiting life-sustaining measures were significantly more frequent in immunocompromised patients (27.1% vs 18.6%; p < 0.0001). Use of noninvasive ventilation (NIV) as first-line treatment was higher in immunocompromised patients (20.9% vs 15.9%; p = 0.0048), and immunodeficiency remained independently associated with the use of NIV after adjustment for confounders. Forty-eight percent of the patients treated with NIV were intubated, and their mortality was not different from that of the patients invasively ventilated ab initio. Conclusions: Immunosuppression is frequent in patients with ARDS, and infections are the main risk factors for ARDS in these immunocompromised patients. Their management differs from that of immunocompetent patients, particularly the greater use of NIV as first-line ventilation strategy. Compared with immunocompetent subjects, they have higher mortality regardless of ARDS severity as well as a higher frequency of limitation of life-sustaining measures. Nonetheless, nearly half of these patients survive to hospital discharge. Trial registration: ClinicalTrials.gov, NCT02010073. Registered on 12 December 2013

Resolved versus confirmed ARDS after 24&#160;h: insights from the LUNG SAFE study

Purpose: To evaluate patients with resolved versus confirmed ARDS, identify subgroups with substantial mortality risk, and to determine the utility of day 2 ARDS reclassification. Methods: Our primary objective, in this secondary LUNG SAFE analysis, was to compare outcome in patients with resolved versus confirmed ARDS after 24\ua0h. Secondary objectives included identifying factors associated with ARDS persistence and mortality, and the utility of day 2 ARDS reclassification. Results: Of 2377 patients fulfilling the ARDS definition on the first day of ARDS (day 1) and receiving invasive mechanical ventilation, 503 (24%) no longer fulfilled the ARDS definition the next day, 52% of whom initially had moderate or severe ARDS. Higher tidal volume on day 1 of ARDS was associated with confirmed ARDS [OR 1.07 (CI 1.01\u20131.13), P = 0.035]. Hospital mortality was 38% overall, ranging from 31% in resolved ARDS to 41% in confirmed ARDS, and 57% in confirmed severe ARDS at day 2. In both\ua0resolved and confirmed\ua0ARDS, age, non-respiratory SOFA score, lower PEEP and P/F ratio, higher peak pressure and respiratory rate were each\ua0associated with mortality. In confirmed ARDS, pH and the presence of immunosuppression or neoplasm were also associated\ua0with mortality. The increase in area under the receiver operating curve for ARDS reclassification on day 2 was marginal. Conclusions: ARDS, whether resolved or confirmed at day 2, has a high mortality rate. ARDS reclassification at day 2 has limited predictive value for mortality. The substantial mortality risk in severe confirmed ARDS suggests that complex interventions might best be tested in this population. Trial Registration: ClinicalTrials.gov NCT02010073. \ua9 2018, Springer-Verlag GmbH Germany, part of Springer Nature and ESICM

Death in hospital following ICU discharge : insights from the LUNG SAFE study

Altres ajuts: Italian Ministry of University and Research (MIUR)-Department of Excellence project PREMIA (PREcision MedIcine Approach: bringing biomarker research to clinic); Science Foundation Ireland Future Research Leaders Award; European Society of Intensive Care Medicine (ESICM), Brussels; St Michael's Hospital, Toronto; University of Milan-Bicocca, Monza, Italy.Background: To determine the frequency of, and factors associated with, death in hospital following ICU discharge to the ward. Methods: The Large observational study to UNderstand the Global impact of Severe Acute respiratory FailurE study was an international, multicenter, prospective cohort study of patients with severe respiratory failure, conducted across 459 ICUs from 50 countries globally. This study aimed to understand the frequency and factors associated with death in hospital in patients who survived their ICU stay. We examined outcomes in the subpopulation discharged with no limitations of life sustaining treatments ('treatment limitations'), and the subpopulations with treatment limitations. Results: 2186 (94%) patients with no treatment limitations discharged from ICU survived, while 142 (6%) died in hospital. 118 (61%) of patients with treatment limitations survived while 77 (39%) patients died in hospital. Patients without treatment limitations that died in hospital after ICU discharge were older, more likely to have COPD, immunocompromise or chronic renal failure, less likely to have trauma as a risk factor for ARDS. Patients that died post ICU discharge were less likely to receive neuromuscular blockade, or to receive any adjunctive measure, and had a higher pre- ICU discharge non-pulmonary SOFA score. A similar pattern was seen in patients with treatment limitations that died in hospital following ICU discharge. Conclusions: A significant proportion of patients die in hospital following discharge from ICU, with higher mortality in patients with limitations of life-sustaining treatments in place. Non-survivors had higher systemic illness severity scores at ICU discharge than survivors. Trial Registration: ClinicalTrials.gov NCT02010073

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