675 research outputs found

    The f-electron challenge: localized and itinerant states in lanthanide oxides united by GW@LDA+U

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    Many-body perturbation theory in the GW approach is applied to lanthanide oxides, using the local-density approximation plus a Hubbard U correction (LDA+U) as the starting point. Good agreement between the G0W0 density of states and experimental spectra is observed for CeO2 and Ce2O3. Unlike the LDA+U method G0W0 exhibits only a weak dependence on U in a physically meaningful range of U values. For the whole lanthanide sesquioxide (Ln2O3) series G0W0@LDA+U reproduces the main features found for the optical experimental band gaps. The relative positions of the occupied and unoccupied f-states predicted by G0W0 confirm the experimental conjecture derived from phenomenological arguments.Comment: 4 pages including 3 figures; related publications can be found at http://www.fhi-berlin.mpg.de/th/th.htm

    Responses of Arctic cyclones to biogeophysical feedbacks under future warming scenarios in a regional Earth system model

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    Arctic cyclones, as a prevalent feature in the coupled dynamics of the Arctic climate system, have large impacts on the atmospheric transport of heat and moisture and deformation and drifting of sea ice. Previous studies based on historical and future simulations with climate models suggest that Arctic cyclogenesis is affected by the Arctic amplification of global warming, for instance, a growing land-sea thermal contrast. We thus hypothesize that biogeophysical feedbacks (BF) over the land, here mainly referring to the albedo-induced warming in spring and evaporative cooling in summer, may have the potential to significantly change cyclone activity in the Arctic. Based on a regional Earth system model (RCA-GUESS) which couples a dynamic vegetation model and a regional atmospheric model and an algorithm of cyclone detection and tracking, this study assesses for the first time the impacts of BF on the characteristics of Arctic cyclones under three IPCC Representative Concentration Pathways scenarios (i.e. RCP2.6, RCP4.5 and RCP8.5). Our analysis focuses on the spring- and summertime periods, since previous studies showed BF are the most pronounced in these seasons. We find that BF induced by changes in surface heat fluxes lead to changes in land-sea thermal contrast and atmospheric stability. This, in turn, noticeably changes the atmospheric baroclinicity and, thus, leads to a change of cyclone activity in the Arctic, in particular to the increase of cyclone frequency over the Arctic Ocean in spring. This study highlights the importance of accounting for BF in the prediction of Arctic cyclones and the role of circulation in the Arctic regional Earth system

    First-principles study of structural, electronic and thermodynamic properties of (ZnO)n_n(n=2-16) clusters

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    The structural, electronic, and vibrational thermodynamic properties of the (ZnO)n_n (n=2-16) clusters are studied using density functional - full potential computations. The results show, small clusters up to n=9n=9 stabilize in the 2D ring shape geometries while the larger clusters prefer the 3D cage like structures. The ring to cage structural cross over in ZnO clusters is studied by investigating the behavior of the Zn-O-Zn bond angle, the Zn-O bond strength, and the number of bonds in the systems. It is argued that 12 is the lowest magic number of ZnO clusters at ground state, while finite temperature vibrational excitations enhance the relative stability of the (ZnO)9_9 cluster and make it a magic system at temperatures above about 170 K. The obtained electronic structure of ZnO clusters before and after applying the many-body GW corrections evidence a size induced red shift originated from the ring to cage structural cross over in these systems. The behavior of the extremal points of electron density of the clusters along with the extrapolated cluster binding energies at very large sizes may be evidences for existence of a metastable structure for large ZnO nanostructures, different with the bulk ZnO structure.Comment: 8 pages, 8 figures and 1 tabl

    (Re)Conceptualizing decision-making tools in a risk governance framework for emerging technologies—the case of nanomaterials

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    The utility of decision-making tools for the risk governance of nanotechnology is at the core of this paper. Those working in nanotechnology risk management have been prolific in creating such tools, many derived from European FP7 and H2020-funded projects. What is less clear is how such tools might assist the overarching ambition of creating a fair system of risk governance. In this paper, we reflect upon the role that tools might and should play in any system of risk governance. With many tools designed for the risk governance of this emerging technology falling into disuse, this paper provides an overview of extant tools and addresses their potential shortcomings. We also posit the need for a data readiness tool. With the EUs NMP13 family of research consortia about to report to the Commission on ways forward in terms of risk governance of this domain, this is a timely intervention on an important element of any risk governance system

    Hypoglycaemia induces a sustained pro-inflammatory response in people with type 1 diabetes and healthy controls

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    Aim: To determine the duration and the extension of the pro-inflammatory response to hypoglycaemia both in people with type 1 diabetes and healthy controls. Materials and Methods: Adults with type 1 diabetes (n = 47) and matched controls (n = 16) underwent a hyperinsulinaemic-euglycaemic hypoglycaemic (2.8 ± 0.1 mmoL/L [49.9 ± 2.3 mg/dL]) glucose clamp. During euglycaemia, hypoglycaemia, and 1, 3 and 7 days later, blood was drawn to determine immune cell phenotype, monocyte function and circulating inflammatory markers. Results: Hypoglycaemia increased lymphocyte and monocyte counts, which remained elevated for 1 week. The proportion of CD16+ monocytes increased and the proportion of CD14+ monocytes decreased. During hypoglycaemia, monocytes released more tumour necrosis factor-a and interleukin-1ß, and less interleukin-10, after ex vivo stimulation. Hypoglycaemia increased the levels of 19 circulating inflammatory proteins, including high sensitive C-reactive protein, most of which remained elevated for 1 week. The epinephrine peak in response to hypoglycaemia was positively correlated with immune cell number and phenotype, but not with the proteomic response. Conclusions: Overall, despite differences in prior exposure to hypoglycaemia, the pattern of the inflammatory responses to hypoglycaemia did not differ between people with type 1 diabetes and healthy controls. In conclusion, hypoglycaemia induces a range of pro-inflammatory responses that are sustained for at least 1 week in people with type 1 diabetes and healthy controls

    The impact of prior exposure to hypoglycaemia on the inflammatory response to a subsequent hypoglycaemic episode

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    BACKGROUND: Hypoglycaemia has been shown to induce a systemic pro-inflammatory response, which may be driven, in part, by the adrenaline response. Prior exposure to hypoglycaemia attenuates counterregulatory hormone responses to subsequent hypoglycaemia, but whether this effect can be extrapolated to the pro-inflammatory response is unclear. Therefore, we investigated the effect of antecedent hypoglycaemia on inflammatory responses to subsequent hypoglycaemia in humans.METHODS: Healthy participants (n = 32) were recruited and randomised to two 2-h episodes of either hypoglycaemia or normoglycaemia on day 1, followed by a hyperinsulinaemic hypoglycaemic (2.8 ± 0.1 mmol/L) glucose clamp on day 2. During normoglycaemia and hypoglycaemia, and after 24 h, 72 h and 1 week, blood was drawn to determine circulating immune cell composition, phenotype and function, and 93 circulating inflammatory proteins including hs-CRP.RESULTS: In the group undergoing antecedent hypoglycaemia, the adrenaline response to next-day hypoglycaemia was lower compared to the control group (1.45 ± 1.24 vs 2.68 ± 1.41 nmol/l). In both groups, day 2 hypoglycaemia increased absolute numbers of circulating immune cells, of which lymphocytes and monocytes remained elevated for the whole week. Also, the proportion of pro-inflammatory CD16+-monocytes increased during hypoglycaemia. After ex vivo stimulation, monocytes released more TNF-α and IL-1β, and less IL-10 in response to hypoglycaemia, whereas levels of 19 circulating inflammatory proteins, including hs-CRP, increased for up to 1 week after the hypoglycaemic event. Most of the inflammatory responses were similar in the two groups, except the persistent pro-inflammatory protein changes were partly blunted in the group exposed to antecedent hypoglycaemia. We did not find a correlation between the adrenaline response and the inflammatory responses during hypoglycaemia.CONCLUSION: Hypoglycaemia induces an acute and persistent pro-inflammatory response at multiple levels that occurs largely, but not completely, independent of prior exposure to hypoglycaemia. Clinical Trial information Clinicaltrials.gov no. NCT03976271 (registered 5 June 2019).</p

    The impact of prior exposure to hypoglycaemia on the inflammatory response to a subsequent hypoglycaemic episode

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    BACKGROUND: Hypoglycaemia has been shown to induce a systemic pro-inflammatory response, which may be driven, in part, by the adrenaline response. Prior exposure to hypoglycaemia attenuates counterregulatory hormone responses to subsequent hypoglycaemia, but whether this effect can be extrapolated to the pro-inflammatory response is unclear. Therefore, we investigated the effect of antecedent hypoglycaemia on inflammatory responses to subsequent hypoglycaemia in humans.METHODS: Healthy participants (n = 32) were recruited and randomised to two 2-h episodes of either hypoglycaemia or normoglycaemia on day 1, followed by a hyperinsulinaemic hypoglycaemic (2.8 ± 0.1 mmol/L) glucose clamp on day 2. During normoglycaemia and hypoglycaemia, and after 24 h, 72 h and 1 week, blood was drawn to determine circulating immune cell composition, phenotype and function, and 93 circulating inflammatory proteins including hs-CRP.RESULTS: In the group undergoing antecedent hypoglycaemia, the adrenaline response to next-day hypoglycaemia was lower compared to the control group (1.45 ± 1.24 vs 2.68 ± 1.41 nmol/l). In both groups, day 2 hypoglycaemia increased absolute numbers of circulating immune cells, of which lymphocytes and monocytes remained elevated for the whole week. Also, the proportion of pro-inflammatory CD16+-monocytes increased during hypoglycaemia. After ex vivo stimulation, monocytes released more TNF-α and IL-1β, and less IL-10 in response to hypoglycaemia, whereas levels of 19 circulating inflammatory proteins, including hs-CRP, increased for up to 1 week after the hypoglycaemic event. Most of the inflammatory responses were similar in the two groups, except the persistent pro-inflammatory protein changes were partly blunted in the group exposed to antecedent hypoglycaemia. We did not find a correlation between the adrenaline response and the inflammatory responses during hypoglycaemia.CONCLUSION: Hypoglycaemia induces an acute and persistent pro-inflammatory response at multiple levels that occurs largely, but not completely, independent of prior exposure to hypoglycaemia. Clinical Trial information Clinicaltrials.gov no. NCT03976271 (registered 5 June 2019).</p

    Investigating sociophysical attributes underlying train boarding efficiency and their importance for nudging

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    Nudging has become a popular method to change the behavior of pedestrians in public spaces. However, nudges often do not work as intended because they are based on an incomplete understanding of the nudging environment, physical (e.g., pedestrian trajectories), but not psychological data is used in their development, and behavioral theories are often inadequate or not (correctly) applied. In this article, we argue that the design of nudges can benefit from complementary psychological data analyzed using relevant social and environmental psychological theories. Adequate theories, we argue, are those that aim at describing the objective (i.e., person independent) attributes of the environment or situation and how these affect human decision-making. Using the example of train boarding, and in particular the formation of the deboarding corridor, we demonstrate how psychological theories like interdependence theory and social norms theory can be applied to relevant psychological data—in our case obtained with two focus groups—to better characterize the sociophysical attributes of the train boarding situation. The focus group, or sometimes called a “group discussion”, is a qualitative research method in which data is generated from guided discussions amongst research participants following pre-defined discussion topics. Based on the thematic analysis of the focus group data, we find that a high level of competition and interdependence are related to structural aspects of the train boarding situation. Subsequently, we use these insights to provide tentative explanations for, or hypotheses about micro- and macroscopic behavior patterns observed during train boarding. Finally, we discuss how these insights, in turn, can inform the design of nudges that can be further investigated in future research.</p

    Gauge Theory of the String Geodesic Field

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    A relativistic string is usually represented by the Nambu-Goto action in terms of the extremal area of a 2-dimensional timelike submanifold of Minkowski space. Alternatively, a family of classical solutions of the string equation of motion can be globally described in terms of the associated geodesic field. In this paper we propose a new gauge theory for the geodesic field of closed and open strings. Our approach solves the technical and conceptual problems affecting previous attempts to describe strings in terms of local field variables. The connection between the geodesic field, the string current and the Kalb-Ramond gauge potential is discussed and clarified. A non-abelian generalization and the generally covariant form of the model are also discussed.Comment: 38 pages, PHYZZX, UTS-DFT-92-2
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