4,933 research outputs found

    Landau Theory of the Finite Temperature Mott Transition

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    In the context of the dynamical mean-field theory of the Hubbard model, we identify microscopically an order parameter for the finite temperature Mott endpoint. We derive a Landau functional of the order parameter. We then use the order parameter theory to elucidate the singular behavior of various physical quantities which are experimentally accessible.Comment: 4 pages, 2 figure

    Dilution of the magnetic lattice in the Kitaev candidate α\alpha-RuCl3_3 by Rh3+^{3+} doping

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    Magnetic dilution of a well-established Kitaev candidate system is realized in the substitutional Ru1−x_{1-x}Rhx_xCl3_3 series (x=0.02−0.6x = 0.02-0.6). Optimized syntheses protocols yield uniformly-doped single crystals and polycrystalline powders that are isostructural to the parental α\alpha-RuCl3_3 as per X-ray diffraction. The Rh content xx is accurately determined by the quantitative energy-dispersive X-ray spectroscopy technique with standards. We determine the magnetic phase diagram of Ru1−x_{1-x}Rhx_xCl3_3 for in-plane magnetic fields from magnetization and specific-heat measurements as a function of xx and stacking periodicity, and identify the suppression of the magnetic order at x≈0.2x \approx 0.2 towards a disordered phase, which does not show any clear signature of freezing into a spin glass. Comparing with previous studies on the substitution series Ru1−x_{1-x}Irx_xCl3_3, we propose that chemical pressure would contribute to the suppression of magnetic order especially in Ru1−x_{1-x}Irx_xCl3_3 and that the zigzag magnetic ground state appears to be relatively robust with respect to the dilution of the Kitaev--Γ\Gamma--Heisenberg magnetic lattice. We also discovered a slight dependence of the magnetic properties on thermal cycling, which would be due to an incomplete structural transition

    Huisartsgeneeskundige zorg in het verzorgingshuis

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    Een deel van de Nederlandse huisartsenzorg bestaat uit zorg voor ouderen in verzorgingshuizen. We vergelijken de huisartsenzorg aan patiënten in deze verzorgingshuizen met die aan leeftijdsgenoten die zelfstandig, buiten het verzorgingshuis, wonen. Omdat mensen langer zelfstandig wonen en de indicatiestelling voor plaatsing in een verzorgingshuis op basis van slecht functioneren in ADL gebeurt, verwachtten we een groep ouderen te vinden in het verzorgingshuis die meer complexe zorg behoeft van de huisarts. Het onderzoek is een ‘matched case-control’-studie in 3 Nederlandse huisartspraktijken in de periode 1/1/1998 tot 1/7/2004. De belangrijkste resultaten zijn dat de prevalentie van cognitieve problemen twee keer zo hoog en de prevalentie van depressie drie keer zo hoog is in de groep verzorgingshuisbewoners vergeleken met hun zelfstandig wonende leeftijdsgenoten. Problemen van het bewegingsapparaat worden ook veel gezien in de verzorgingshuizen. Chronische longproblemen, hart- en vaatziekten (excl. CVA) en urineweginfecties komen meer voor, maar CVA, diabetes en kanker komen juist evenveel voor binnen en buiten het verzorgingshuis. Geïnstitutionaliseerde ouderen gebruiken gemiddeld meer medicamenten tegelijkertijd. De conclusie is dat de huisarts in het verzorgingshuis te maken heeft met een specifieke kwetsbare groep ouderen waarbij de zorg niet beperkt is tot de behandeling van chronische aandoeningen, maar meer gericht is op het complexe samenspel van ziekte, afnemende functionele en cognitieve status en het levensperspectief van kwetsbare ouderen in het verzorgingshuis

    Expression dynamics of genes in the hypothalamic-pituitary-thyroid (HPT) cascade and their responses to 3,3′,5-triiodo-L-thyronine (T3) highlights potential vulnerability to thyroid-disrupting chemicals in zebrafish (Danio rerio) embryo-larvae

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    This is the author accepted manuscriptSome chemicals in the environment disrupt thyroid hormone (TH) systems leading to alterations in organism development, but their effect mechanisms are poorly understood. In fish, this has been limited by a lack of fundamental knowledge on thyroid gene ontogeny and tissue expression in early life stages. Here we established detailed expression profiles for a suite of genes in the hypothalamic-pituitary-thyroid (HPT) axis of zebrafish (Danio rerio) between 24-120 hours post fertilisation (hpf) and quantified their responses following exposure to 3,3’,5-triiodo-L-thyronine (T3) using whole mount in situ hybridisation (WISH) and qRT-PCR (of whole-body extracts). All of the selected genes in the HPT axis demonstrated dynamic transcript expression profiles across the developmental stages examined. The expression of thyroid receptor alpha (thraa) was observed in the brain, gastrointestinal tract, craniofacial tissues and pectoral fins, while thyroid receptor beta (thrb) expression occurred in the brain, otic vesicles, liver and lower jaw. The TH deiodinases (dio1, dio2 and dio3b) were expressed in the liver, pronephric ducts and brain and the patterns differed depending on life stage. Both dio1 and dio2 were also expressed in the intestinal bulb (96-120 hpf), and dio2 expression occurred also in the pituitary (48-120 hpf). Exposure of zebrafish embryo-larvae to T3 (30 and 100 μg L-1) for periods of 48, 96 or 120 hpf resulted in the up-regulation of thraa, thrb, dio3b, thyroid follicle synthesis proteins (pax8) and corticotropin-releasing hormone (crhb) and down-regulation of dio1, dio2, glucuronidation enzymes (ugt1ab) and thyroid stimulating hormone (tshb) (assessed via qRT-PCR) and responses differed across life stage and tissues. T3 induced thraa expression in the pineal gland, pectoral fins, brain, somites, gastrointestinal tract, craniofacial tissues, liver and pronephric ducts. T3 enhanced thrb expression in the brain, jaw cartilage and intestine, while thrb expression was suppressed in the liver. T3 exposure suppressed the transcript levels of dio1 and dio2 in the liver, brain, gastrointestinal tract and craniofacial tissues, while dio2 signalling was also suppressed in the pituitary gland. Dio3b expression was induced by T3 exposure in the jaw cartilage, pectoral fins and brain. The involvement of THs in the development of numerous body tissues and the responsiveness of these tissues to T3 in zebrafish highlights their potential vulnerability to exposure to environmental thyroid-disrupting chemicals.Department of Environment, Food and Rural AffairsUniversity of Exete

    Molecular mechanisms and tissue targets of brominated flame retardants, BDE-47 and TBBPA, in embryo-larval life stages of zebrafish (Danio rerio).

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    Brominated flame retardants are known to disrupt thyroid hormone (TH) homeostasis in several vertebrate species, but the molecular mechanisms underlying this process and their effects on TH-sensitive tissues during the stages of early development are not well characterised. In this study, we exposed zebrafish (Danio rerio) embryo-larvae to 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) and tetrabromobisphenol A (TBBPA) via the water for 96 h from fertilisation and assessed for lethality, effects on development and on the expression of a suite of genes in the hypothalamic-pituitary-thyroid (HPT) axis via both real time quantitative PCR (qRT-PCR) on whole body extracts and whole mount in situ hybridisation (WISH) to identify tissue targets. The 96-h lethal median concentration (96h-LC50) for TBBPA was 0.9 μM and mortality was preceded by retardation of development (smaller animals) and morphological deformities including, oedemas in the pericardial region and tail, small heads, swollen yolk sac extension. Exposure to BDE-47 did not affect zebrafish embryo-larvae survival at any of the concentrations tested (1-100 μM) but caused yolk sac and craniofacial deformities, a curved spine and shorter tail at the highest exposure concentration. TBBPA exposure resulted in higher levels of mRNAs for genes encoding deiodinases (dio1), transport proteins (ttr), the thyroid follicle synthesis protein paired box 8 (pax8) and glucuronidation enzymes (ugt1ab) and lower levels of dio3b mRNAs in whole body extracts, with responses varying with developmental stage. BDE-47 exposure resulted in higher levels of thrb, dio1, dio2, pax8 and ugt1ab mRNAs and lower levels of ttr mRNAs in whole body extracts. TBBPA and BDE-47 therefore appear to disrupt the TH system at multiple levels, increasing TH conjugation and clearance, disrupting thyroid follicle development and altering TH transport. Compensatory responses in TH production/ metabolism by deiodinases were also evident. WISH analyses further revealed that both TBBPA and BDE-47 caused tissue-specific changes in thyroid receptor and deiodinase enzyme expression, with the brain, liver, pronephric ducts and craniofacial tissues appearing particularly responsive to altered TH signalling. Given the important role of TRs in mediating the actions of THs during key developmental processes and deiodinases in the control of peripheral TH levels, these transcriptional alterations may have implications for TH sensitive target genes involved in brain and skeletal development. These findings further highlight the potential vulnerability of the thyroid system to disruption by BFRs during early developmental windows

    Spin-Momentum Correlations in Quasi-Elastic Electron Scattering from Deuterium

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    We report on a measurement of spin-momentum correlations in quasi-elastic scattering of longitudinally polarized electrons with an energy of 720 MeV from vector-polarized deuterium. The spin correlation parameter AedVA^V_{ed} was measured for the 2H⃗(e⃗,e′p)n^2 \vec{\rm H}(\vec e,e^\prime p)n reaction for missing momenta up to 350 MeV/cc at a four-momentum transfer squared of 0.21 (GeV/c)2^2. The data give detailed information about the spin structure of the deuteron, and are in good agreement with the predictions of microscopic calculations based on realistic nucleon-nucleon potentials and including various spin-dependent reaction mechanism effects. The experiment demonstrates in a most direct manner the effects of the D-state in the deuteron ground-state wave function and shows the importance of isobar configurations for this reaction.Comment: 4 pages, 3 figures, submitted to Phys. Rev. Lett. for publicatio

    Design and feasibility testing of a novel group intervention for young women who binge drink in groups

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    BackgroundYoung women frequently drink alcohol in groups and binge drinking within these natural drinking groups is common. This study describes the design of a theoretically and empirically based group intervention to reduce binge drinking among young women. It also evaluates their engagement with the intervention and the acceptability of the study methods.MethodsFriendship groups of women aged 18–35 years, who had two or more episodes of binge drinking (>6 UK units on one occasion; 48g of alcohol) in the previous 30 days, were recruited from the community. A face-to-face group intervention, based on the Health Action Process Approach, was delivered over three sessions. Components of the intervention were woven around fun activities, such as making alcohol free cocktails. Women were followed up four months after the intervention was delivered. Results The target of 24 groups (comprising 97 women) was recruited. The common pattern of drinking was infrequent, heavy drinking (mean consumption on the heaviest drinking day was UK 18.1 units). Process evaluation revealed that the intervention was delivered with high fidelity and acceptability of the study methods was high. The women engaged positively with intervention components and made group decisions about cutting down. Twenty two groups set goals to reduce their drinking, and these were translated into action plans. Retention of individuals at follow up was 87%.ConclusionsThis study successfully recruited groups of young women whose patterns of drinking place them at high risk of acute harm. This novel approach to delivering an alcohol intervention has potential to reduce binge drinking among young women. The high levels of engagement with key steps in the behavior change process suggests that the group intervention should be tested in a full randomised controlled trial

    B→D(∗)B \to D^{(*)} Form Factors from QCD Light-Cone Sum Rules

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    We derive new QCD sum rules for B→DB\to D and B→D∗B\to D^* form factors. The underlying correlation functions are expanded near the light-cone in terms of BB-meson distribution amplitudes defined in HQET, whereas the cc-quark mass is kept finite. The leading-order contributions of two- and three-particle distribution amplitudes are taken into account. From the resulting light-cone sum rules we calculate all B\to \Dst form factors in the region of small momentum transfer (maximal recoil). In the infinite heavy-quark mass limit the sum rules reduce to a single expression for the Isgur-Wise function. We compare our predictions with the form factors extracted from experimental B\to \Dst l \nu_l decay rates fitted to dispersive parameterizations.Comment: 20 pages, 6 figures; one reference, one figure and several comments added; version to appear in European Physical Journal
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