581 research outputs found

    Nuclear structure of the semi-magic tin isotopes close to 100Sn: lifetime measurements of low-lying states in 106Sn and 108Sn

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    The structure of nuclei with few nucleons outside the double-shell closure Z=N =50 has attracted large theoretical and experimental interest in the last years. Several studies were performed in this region to examine the evolution of the nucleon-nucleon interaction when going towards 100Sn and eventually deduce the proton shell closure. Along the whole isotopic chain the excitation energy of the first 2+ and 4+ states is well known and the behaviour is rather constant. Then, for neutron-rich Sn isotopes the reduced transition probability seems to follow the parabolic behavior with the maximum at the mid shell, which is the typical trend that one would expect for one-body even operator, such as the B(E2). However, the information on the B(E2; 2+→0+) values for the neutron-deficient Sn isotopes suffer from large experimental uncertainties. Moreover there is a lack of information on the B(E2; 4+→2+), while their values would help to make a more robust physical interpretation. Since now theoretical calculations have been performed during the last decades, but up to date none of them is able to reproduce consistently the trend of the experimental reduced transition probabilities for the full Sn isotopic chain. The experiment discussed in this thesis was devoted to the measurement of the lifetimes of the low-lying states 2+ and 4+ for 106,108Sn, in order to derive the reduced transition probabilities B(E2), by using the Recoil Distance Doppler-Shift (RDDS) method. The nuclei of interest were populated via multi nucleon transfer reaction where a 106Cd beam, provided by one separated-sector cyclotron of the GANIL facility (France) at the energy of 770 MeV, impinged onto a 92Mo target. After the target a 24Mg foil was used as degrader for slowing down the reaction products. This measurement is complementary to the Coulomb excitation method and it represents the very first direct lifetime measurement in the neutron-deficient Sn isotopes. The complete identification of the reaction products was obtained on an event-by-event basis using the VAMOS++ magnetic spectrometer. In coincidence with VAMOS++, gamma rays were detected by 8 AGATA Triple Clusters. Thanks to the combination of the magnetic spectrometer together with the choice of the reaction mechanism, it was also possible to reconstruct the Q-value of the reaction. Such information was crucial for the success of the lifetime measurement because it allowed to control the feeding from higher-lying states. Finally it was possible to measure the lifetimes of the 2+ and 4+ excited states for 106,108 Sn. In order to reduce the error, for 108Sn several tests on both Decay-Curve Method (DCM) and Differential Decay-Curve Method (DDCM) are discussed. The reduced transition probabilities B(E2), deduced from the measured lifetimes, were compared with Large-Scale Shell-Model (LSSM) calculations. Such basic nuclear feature have proved to be incredibly sensible to the form of the wave function: in particular the new B(E2; 4+→2+) value of 108Sn clearly showed that high seniority components of the wave function are of extreme importance to define the transition probabilities in this region. This result questions the validity of other theoretical predictions, which have been considering the seniority truncation, in reproducing consistently the trend of the experimental B(E2) values

    On fractional Choquard equations

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    We investigate a class of nonlinear Schrodinger equations with a generalized Choquard nonlinearity and fractional diffusion. We obtain regularity, existence, nonexistence, symmetry as well as decays properties.Comment: revised version, 22 page

    Rare earth elements in human and animal health: State of art and research priorities

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    "Background: A number of applications have been developed using rare earth elements (REE), implying several human exposures and raising unsolved questions as to REE-associated health effects. Methods: A MedLine survey was retrieved from early reports (1980s) up to June 2015, focused on human and animal exposures to REE. Literature from animal models was selected focusing on REE-associated health effects. Results: Some REE occupational exposures, in jobs such as glass polishers, photoengravers and movie projectionists showed a few case reports on health effects affecting the respiratory system. No case-control or cohort studies of occupational REE exposures were retrieved. Environmental exposures have been biomonitored in populations residing in REE mining areas, showing REE accumulation. The case for a iatrogenic REE exposure was raised by the use of gadolinium-based contrast agents for nuclear magnetic resonance. Animal toxicity studies have shown REE toxicity, affecting a number of endpoints in liver, lungs and blood. On the other hand, the use of REE as feed additives in livestock is referred as a safe and promising device in zootechnical activities, possibly suggesting a hormetic effect both known for REE and for other xenobiotics. Thus, investigations on long-term exposures and observations are warranted. Conclusion: The state of art provides a limited definition of the health effects in occupationally or environmentally REE-exposed human populations. Research priorities should be addressed to case-control or cohort studies of REE-exposed humans and to life-long animal experiments. (C) 2015 Elsevier Inc. All rights reserved.

    An Ecotoxicological Evaluation of Four Fungal Metabolites with Potential Application as Biocides for the Conservation of Cultural Heritage

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    Biocides based on chemical synthetic compounds have been commonly used to counteract damages caused by microorganisms on stone cultural heritage. However, in the last few years, the use of commercial and traditional biocides has been banned and/or limited due to their dangerous profile for the environment, as well as human and animal health. Natural products could be used as suitable alternatives for cultural heritage purposes, as they have low toxicity and stability compared with synthetic pesticides. Even if most of the investigated solutions have already shown promising results, their efficiency, ecotoxicological, and chemical features are poorly investigated. In this manuscript, we aimed to evaluate the ecotoxicological profile of four fungal metabolites—namely, cavoxin, epiepoformin, seiridin, and sphaeropsidone—with potential antimicrobial properties for monumental artworks. A battery of ecotoxicological tests using Aliivibrio fischeri (bacterium), Raphidocelis subcapitata (alga), Raphanus sativus L. (macrophyte), Daphnia magna (crustacean), and Caenorhabditis elegans (nematode) revealed a relative lower toxicity of these compounds, especially when compared with Preventol® and Rocima®, commercial biocides mainly used for the conservation of cultural heritage

    Comparative toxicities of selected rare earth elements: Sea urchin embryogenesis and fertilization damage with redox and cytogenetic effects

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    Background: Broad-rangingadverseeffectsareknownforrareearthelements(REE),yetonlyafew studies testedthetoxicityofseveralREE,promptingstudiesfocusingonmulti-parameterREEtoxicity. Methods: TrichloridesaltsofY,La,Ce,Nd,Sm,EuandGdweretestedin Paracentrotuslividus sea urchin embryos andspermfor:(1)developmentaldefectsineitherREE-exposedlarvaeorintheoffspringof REE-exposedsperm;(2)fertilizationsuccess;(3)mitoticanomaliesinREE-exposedembryosandinthe offspring ofREE-exposedsperm,and(4)reactiveoxygenspecies(ROS)formation,andmalondialdehyde (MDA)andnitricoxide(NO)levels. Results: REEs affected P.lividus larvaewithconcentration-relatedincreaseindevelopmentaldefects, 106 to 104 M, rankingas:Gd(III)4Y(III)4La(III)4Nd(III)≅Eu(III)4Ce(III)≅Sm(III). Nominalcon- centrations ofREEsaltswereconfirmed byinductivelycoupledplasmamassspectrometry(ICP-MS). Significant increasesinMDAlevels,ROSformation,andNOlevelswerefoundinREE-exposedembryos. Sperm exposuretoREEs(105 to 104 M) resultedinconcentration-relateddecreaseinfertilization success alongwithincreaseinoffspringdamage.Decreasedmitoticactivityandincreasedaberration ratesweredetectedinREE-exposedembryosandintheoffspringofREE-exposedsperm. Conclusion: REE-associated toxicityaffectingembryogenesis,fertilization,cytogeneticandredoxend- points showeddifferentactivitiesoftestedREEs.Damagetoearlylifestages,alongwithredoxandcy- togeneticanomaliesshouldbethefocusoffutureREEtoxicitystudies

    Removal of antiretroviral drugs stavudine and zidovudine in water under UV<sub>254</sub> and UV<sub>254</sub>/H<sub>2</sub>O<sub>2</sub> processes:Quantum yields, kinetics and ecotoxicology assessment

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    The concentration of antiretroviral drugs in wastewater treatment plants (WWTP) effluents and surface waters of many countries has increased significantly due to their widespread use for HIV treatment. In this study, the removal of stavudine and zidovudine under UV254 photolysis or UV254/H2O2 was investigated in a microcapillary film (MCF) photoreactor, using minimal water samples quantities. The UV254 quantum yield of zidovudine, (2.357 ± 0.0589)·10-2 mol ein-1 (pH 4.0-8.0), was 28-fold higher that the yield of stavudine (8.34 ± 0.334)·10-4 mol ein-1 (pH 6.0-8.0). The second-order rate constant kOH,iof reaction of hydroxyl radical with the antiretrovirals (UV254/H2O2 process) were determined by kinetics modeling: (9.98 ± 0.68)·108 M-1 s-1 (pH 4.0-8.0) for zidovudine and (2.03 ± 0.18)·109 M-1 s-1 (pH 6.0-8.0) for stavudine. A battery of ecotoxicological tests (i.e. inhibition growth, bioluminescence, mutagenic and genotoxic activity) using bacteria (Aliivibrio fischeri, Salmonella typhimurium), crustacean (Daphnia magna) and algae (Raphidocelis subcapitata) revealed a marked influence of the UV dose on the ecotoxicological activity. The UV254/H2O2 treatment process reduced the ecotoxicological risk associated to direct photolysis of the antiretrovirals aqueous solutions, but required significantly higher UV254 doses (≥2000 mJ cm-2) in comparison to common water UV disinfection processes

    Surface displaced alfa-enolase of Lactobacillus plantarum is a fibronectin binding protein

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    Background: Lactic acid bacteria of the genus Lactobacillus and Bifidobacterium are one of the most important health promoting groups of the human intestinal microbiota. Their protective role within the gut consists in out competing invading pathogens for ecological niches and metabolic substrates. Among the features necessary to provide health benefits, commensal microorganisms must have the ability to adhere to human intestinal cells and consequently to colonize the gut. Studies on mechanisms mediating adhesion of lactobacilli to human intestinal cells showed that factors involved in the interaction vary mostly among different species and strains, mainly regarding interaction between bacterial adhesins and extracellular matrix or mucus proteins. We have investigated the adhesive properties of Lactobacillus plantarum, a member of the human microbiota of healthy individuals. Results: We show the identification of a Lactobacillus plantarum LM3 cell surface protein (48 kDa), which specifically binds to human fibronectin (Fn), an extracellular matrix protein. By means of mass spectrometric analysis this protein was identified as the product of the L. plantarum enoA1 gene, coding the EnoA1 alfa-enolase. Surface localization of EnoA1 was proved by immune electron microscopy. In the mutant strain LM3-CC1, carrying the enoA1 null mutation, the 48 kDa adhesin was not anymore detectable neither by anti-enolase Western blot nor by Fn-overlay immunoblotting assay. Moreover, by an adhesion assay we show that LM3-CC1 cells bind to fibronectin-coated surfaces less efficiently than wild type cells, thus demonstrating the significance of the surface displaced EnoA1 protein for the L. plantarum LM3 adhesion to fibronectin. Conclusion: Adhesion to host tissues represents a crucial early step in the colonization process of either pathogens or commensal bacteria. We demonstrated the involvement of the L. plantarum Eno A1 alfa-enolase in Fn-binding, by studying LM3 and LM3-CC1 surface proteins. Isolation of LM3-CC1 strain was possible for the presence of expressed enoA2 gene in the L. plantarum genome, giving the possibility, for the first time to our knowledge, to quantitatively compare adhesion of wild type and mutant strain, and to assess doubtless the role of L. plantarum Eno A1 as a fibronectin binding protein. © 2009 Castaldo et al; licensee BioMed Central Ltd

    Surface displaced alfa-enolase of Lactobacillus plantarum is a fibronectin binding protein.

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    BACKGROUND: Lactic acid bacteria of the genus Lactobacillus and Bifidobacterium are one of the most important health promoting groups of the human intestinal microbiota. Their protective role within the gut consists in out competing invading pathogens for ecological niches and metabolic substrates. Among the features necessary to provide health benefits, commensal microorganisms must have the ability to adhere to human intestinal cells and consequently to colonize the gut. Studies on mechanisms mediating adhesion of lactobacilli to human intestinal cells showed that factors involved in the interaction vary mostly among different species and strains, mainly regarding interaction between bacterial adhesins and extracellular matrix or mucus proteins. We have investigated the adhesive properties of Lactobacillus plantarum, a member of the human microbiota of healthy individuals. RESULTS: We show the identification of a Lactobacillus plantarum LM3 cell surface protein (48 kDa), which specifically binds to human fibronectin (Fn), an extracellular matrix protein. By means of mass spectrometric analysis this protein was identified as the product of the L. plantarum enoA1 gene, coding the EnoA1 alfa-enolase. Surface localization of EnoA1 was proved by immune electron microscopy. In the mutant strain LM3-CC1, carrying the enoA1 null mutation, the 48 kDa adhesin was not anymore detectable neither by anti-enolase Western blot nor by Fn-overlay immunoblotting assay. Moreover, by an adhesion assay we show that LM3-CC1 cells bind to fibronectin-coated surfaces less efficiently than wild type cells, thus demonstrating the significance of the surface displaced EnoA1 protein for the L. plantarum LM3 adhesion to fibronectin. CONCLUSION: Adhesion to host tissues represents a crucial early step in the colonization process of either pathogens or commensal bacteria. We demonstrated the involvement of the L. plantarum Eno A1 alfa-enolase in Fn-binding, by studying LM3 and LM3-CC1 surface proteins. Isolation of LM3-CC1 strain was possible for the presence of expressed enoA2 gene in the L. plantarum genome, giving the possibility, for the first time to our knowledge, to quantitatively compare adhesion of wild type and mutant strain, and to assess doubtless the role of L. plantarum Eno A1 as a fibronectin binding protein

    A first attempt to evaluate the toxicity to Phaeodactylum tricornutum Bohlin exposed to rare earth elements

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    The increasing use and demand of rare earth elements in many emerging technologies is leading to a potentially higher input to the marine environment. This study compared for the first time the effect of lanthanum (La), cerium (Ce), neodymium (Nd), samarium (Sm), europium (Eu), gadolinium (Gd), dysprosium (Dy), and erbium (Er) to the microalga Phaeodactylum tricornutum Bohlin. The algal growth inhibition was investigated after 72 h of exposure. The median effect concentrations (EC50) ranged from 0.98 mg/L to 13.21 mg/L and elements were ranked as follows: Gd > Ce > Er > La > Eu > Nd > Dy > Sm. The comparison of predicted no effect concentrations (PNEC) for hazard and risk assessment with measured environmental concentrations showed that ecological risks deriving from REEs could be present, but limited to specific environments like estuarine waters. The results support evidence of actions to manage the REE impact in seawater environments, looking to improve the monitoring tailored to the different and dynamic nature of ecosystems

    Disinfection by-Products and Ecotoxic Risk Associated with Hypochlorite Treatment of Tramadol

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    In recent years, many studies have highlighted the consistent finding of tramadol (TRA) in the effluents from wastewater treatment plants (WTPs) and also in some rivers and lakes in both Europe and North America, suggesting that TRA is removed by no more than 36% by specific disinfection treatments. The extensive use of this drug has led to environmental pollution of both water and soil, up to its detection in growing plants. In order to expand the knowledge about TRA toxicity as well as the nature of its disinfection by-products (DBPs), a simulation of the waste treatment chlorination step has been reported herein. In particular, we found seven new by-products, that together with TRA, have been assayed on different living organisms (Aliivibrio fischeri, Raphidocelis subcapitata and Daphnia magna), to test their acute and chronic toxicity. The results reported that TRA may be classified as a harmful compound to some aquatic organisms whereas its chlorinated product mixture showed no effects on any of the organisms tested. All data suggest however that TRA chlorination treatment produces a variety of DBPs which can be more harmful than TRA and a risk for the aquatic environment and human health
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