14 research outputs found

    Increased UV radiation due to polar ozone chemical depletion and vortex occurrences at Southern Sub-polar Latitudes in the period [1997–2005]

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    The variability of total ozone and UV radiation from Total Ozone Mapping Spectrometer (TOMS) measurements is analyzed as a function of polar vortex occurrences over the southern subpolar regions during the 1997–2005 period. The analysis of vortex occurrences showed high interannual variability in the 40° S–60° S latitude band with a longitudinal asymmetry showing the largest frequencies over the 90° W–90° E region. The impact of vortex occurrences on UV radiation and ozone in clear sky conditions was determined from the comparison between the measurements inside the vortex and a climatology obtained from data outside the vortex over the studied period. Clear sky conditions were determined from TOMS reflectivity data. For measurements outside the vortex, clear sky conditions were selected for reflectivity values lower than 7.5%, while for measurements inside the vortex, a relaxed threshold was determined from statistically similar UV values as a function of reflectivity. UV changes and ozone differences from the climatology were analyzed in the 40° S–50° S and 50° S–60° S latitude bands during the spring period (September to November). The largest UV increases and ozone decreases, reaching ~200% and ~65%, respectively, were found in the 50° S–60° S latitude band in September and October. The heterogeneous ozone loss during vortex occurrences was estimated using a chemical transport model. The largest impact of vortex occurrences was found in October with mean UV increase, total ozone decrease and accumulated ozone loss in the 350–650 K range of, respectively, 47%, 30% and 57%. The region close to South America is the most affected by the Antarctic ozone depletion due to the combined effect of large number of vortex occurrences, lower cloud cover and large ozone decrease. This region would be the most vulnerable in case of cloud cover decrease, due to more frequent occurrence of ozone poor air masses during austral spring

    Satellite and ground measurements of solar erythemal UV radiation and ozone in Argentina

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    International audienceSolar erythemal UV radiation incident on Argentina from tropical to high latitude regions has been measured with ground-based instruments as well as with the TOMS instrument on board of the NASA Earth-Probe satellite. These data permit validation of the UV index, a measure of solar risk to UV exposure, forecasted daily by CONAE (Argentina National Commission on Space Activities) and the Argentine National Weather Service. Model calculations of this index are also presented. In addition, we analyzed the UV effects from the Antarctic ozone hole passing over the continental part of the country using TOMS data corrected by a factor derived from the intercomparison of TOMS satellite data with those determined with Southern Hemisphere ground-based spectroradiometers. In this way, we obtained a rather comprehensive description of the amount of erythemal UV radiation and consequently of the UV index for the entire country, as well as the ozone total column and profile (the latter one at Buenos Aires). The results presented in this work were determined through collaboration between the following institutions: GSFC/NASA in USA, Institute Pierre Simon Laplace in France, University of Innsbruck in Austria and CEILAP, IFIR, CONAE, SMN, Universities of Rosario and San Luis in Argentina. The need to use erythemal irradiance and ozone results in Argentina, one of the most exposed regions of the Southern Hemisphere to study the effects of ozone depletion and consequently UV detrimental effects, has been partially covered in the framework of this North–South collaboration

    Some Recent Progresses in Quantum Tomography Realized at INRIM

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    We present some Quantum Tomography related results recently obtained in the Quantum Optics labs of the National Institute of Metrological Research (INRIM). Initially we describe the first experimental implementation of a new protocol for the reconstruction of a photon-number-resolving (PNR) detector’s POVM (Positive Operator-Valued Measure): such a protocol, exploiting the strong quantum correlations of an ancillary state, results more robust and efficient than its classical counterparts. The second part of the paper focuses on the quantum characterization of a transition-edge sensor (TES) based PNR detector, i.e. the experimental tomography of the POVM of a TES, with a method based on a quorum of coherent probes: we show the reconstruction of the POVM elements up to 11 detected photons and 100 incoming photons, demonstrating the linearity of such a device. Finally, we present a method for the experimental reconstruction of the modal structure of multimode optical fields exploiting a single measurement of higher-order photon number autocorrelation functions. We show our reconstructions of up to three different modes per optical state, demonstrating the excellent agreement with the theoretical predictions and the robustness of our method itself. © (2013) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only

    Reduction in leukotriene B4 generation by bronchoalveolar lavage cells in asthma.

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    BACKGROUND--Leukotrienes are inflammatory mediators implicated in the pathogenesis of asthma. The capacity of inflammatory cells within the airways to generate leukotrienes may be altered in asthma. This hypothesis was tested using bronchoalveolar lavage (BAL) to sample cells within the airways from atopic asthmatic and normal subjects, and by measuring their capacity to generate leukotriene B4 (LTB4) and leukotriene C4 (LTC4) in response to A23187, a potent stimulus of leukotriene generation. METHODS--Bronchoalveolar lavage was performed in 12 mild asymptomatic atopic asthmatic patients and 12 normal subjects. Mixed BAL cell aliquots (approximately 80% alveolar macrophages) were incubated with 0-20 microM A23187 for 10 minutes and with 4 microM A23187 for 0-30 minutes, and leukotrienes were measured by radioimmunoassay and high performance liquid chromatography. RESULTS--Mixed BAL cells from asthmatic subjects generated less LTB4 than cells from normal subjects in dose response and time course experiments (area under the curve 81.5 (0.0-228.5) ng.min.10(-6) cells in asthmatic subjects and 197.9 (13.9-935.6) ng.min.10(-6) cells in normal subjects. There were no differences in LTC4 generation between BAL cells from asthmatic and normal subjects. CONCLUSIONS--Generation of LTB4 by BAL cells from atopic asthmatic subjects in response to A23187 was reduced. As the alveolar macrophage is the major source of LTB4 in BAL cells, these results probably reflect reduced generation of LTB4 by alveolar macrophages from asthmatic patients. This may be a consequence of monocyte migration into the lung, or altered alveolar macrophage function in asthma, or both

    Allergen avoidance in the treatment of asthma and atopic disorders

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    Mapping Cortical and Subcortical Asymmetry in Obsessive-Compulsive Disorder: Findings From the ENIGMA Consortium

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    BACKGROUND: Lateralized dysfunction has been suggested in obsessive-compulsive disorder (OCD). However, it is currently unclear whether OCD is characterized by abnormal patterns of brain structural asymmetry. Here we carried out what is by far the largest study of brain structural asymmetry in OCD. METHODS: We studied a collection of 16 pediatric datasets (501 patients with OCD and 439 healthy control subjects), as well as 30 adult datasets (1777 patients and 1654 control subjects) from the OCD Working Group within the ENIGMA (Enhancing Neuro Imaging Genetics through Meta Analysis) Consortium. Asymmetries of the volumes of subcortical structures, and of measures of regional cortical thickness and surface areas, were assessed based on T1-weighted magnetic resonance imaging scans, using harmonized image analysis and quality control protocols. We investigated possible alterations of brain asymmetry in patients with OCD. We also explored potential associations of asymmetry with specific aspects of the disorder and medication status. RESULTS: In the pediatric datasets, the largest case-control differences were observed for volume asymmetry of the thalamus (more leftward; Cohen's d = 0.19) and the pallidum (less leftward; d = -20.21). Additional analyses suggested putative links between these asymmetry patterns and medication status, OCD severity, or anxiety and depression comorbidities. No significant case-control differences were found in the adult datasets. CONCLUSIONS: The results suggest subtle changes of the average asymmetry of subcortical structures in pediatric OCD, which are not detectable in adults with the disorder. These findings may reflect altered neurodevelopmental processes in OCD.N

    Apoptotic cell death in disease-Current understanding of the NCCD 2023.

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    Apoptosis is a form of regulated cell death (RCD) that involves proteases of the caspase family. Pharmacological and genetic strategies that experimentally inhibit or delay apoptosis in mammalian systems have elucidated the key contribution of this process not only to (post-)embryonic development and adult tissue homeostasis, but also to the etiology of multiple human disorders. Consistent with this notion, while defects in the molecular machinery for apoptotic cell death impair organismal development and promote oncogenesis, the unwarranted activation of apoptosis promotes cell loss and tissue damage in the context of various neurological, cardiovascular, renal, hepatic, infectious, neoplastic and inflammatory conditions. Here, the Nomenclature Committee on Cell Death (NCCD) gathered to critically summarize an abundant pre-clinical literature mechanistically linking the core apoptotic apparatus to organismal homeostasis in the context of disease

    Asthma Therapy with Agents Preventing Leukotriene Synthesis or Action

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

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    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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