NNLO Unquenched Calculation of the b Quark Mass

By combining the first unquenched lattice computation of the B-meson binding energy and the two-loop contribution to the lattice HQET residual mass, we determine the (\bar{{MS}}) (b)-quark mass, (\bar{m}_{b}(\bar{m}_{b})). The inclusion of the two-loop corrections is essential to extract (\bar{m}_{b}(\bar{m}_{b})) with a precision of ({\cal O}(\Lambda^{2}_{QCD}/m_{b})), which is the uncertainty due to the renormalon singularities in the perturbative series of the residual mass. Our best estimate is (\bar{m}_{b}(\bar{m}_{b}) = (4.26 \pm 0.09) {\rm GeV}), where we have combined the different errors in quadrature. A detailed discussion of the systematic errors contributing to the final number is presented. Our results have been obtained on a sample of (60) lattices of size (24^{3}\times 40) at (\beta =5.6), using the Wilson action for light quarks and the lattice HQET for the (b) quark, at two values of the sea quark masses. The quark propagators have been computed using the unquenched links generated by the T(\chi)L Collaboration.Comment: 19 pages, 1 figur

Lattice quark masses: a non-perturbative measurement

We discuss the renormalization of different definitions of quark masses in the Wilson and the tree-level improved SW-Clover fermionic action. For the improved case we give the correct relationship between the quark mass and the hopping parameter. Using perturbative and non-perturbative renormalization constants, we extract quark masses in the \MSbar scheme from Lattice QCD in the quenched approximation at $\beta=6.0$, $\beta=6.2$ and $\beta=6.4$ for both actions. We find: \bar{m}^{\MSbar}(2 GeV)=5.7 \pm 0.1 \pm 0.8 MeV, m_s^{\MSbar}(2GeV)= 130 \pm 2 \pm 18 MeV and m_c^{\MSbar}(2 GeV) = 1662\pm 30\pm 230 MeV.Comment: 21 pages, 4 figures, typos corrected, no result change

Quark masses and the chiral condensate with a non-perturbative renormalization procedure

We determine the quark masses and the chiral condensate in the MSbar scheme at NNLO from Lattice QCD in the quenched approximation at beta=6.0, beta=6.2 and beta=6.4 using both the Wilson and the tree-level improved SW-Clover fermion action. We extract these quantities using the Vector and the Axial Ward Identities and non-perturbative values of the renormalization constants. We compare the results obtained with the two methods and we study the O(a) dependence of the quark masses for both actions.Comment: LATTICE98(spectrum), 3 pages, 1 figure, Edinburgh 98/1

Elysia timida (Risso, 1818) three decades of research

Elysia timida (Risso, 1818) three decades of research.— During the last 30 years, studies on Elysia timida (Risso, 1818) have addressed various aspects related to food sources, photosynthetic efficiency of kleptoplasts, population genetics, chemical ecology and reproductive biology, both in the Mediterranean Sea and in the Mar Menor coastal lagoon. E. timida shows a strong specific interaction with Acetabularia acetabulum, retaining functional chloroplasts for at least 45 days and obtaining extra energy in periods when food resources are scarce. It shows control of parapodia, avoiding pigment photodestruction under oversaturated light conditions. The chemical ecological relationships established between E. timida and its potential predator fish, Thalassoma pavo, have also been evaluated, and it has been found that that the extracts of the mollusc contain repellent and unpalatable polypropionate compounds. Population genetics has demonstrated the genetic divergence between populations showing high and significant values of FST and genetic distances, and at least six privative alleles that are not shared with Mediterranean populations have been detected in lagoon populations. This sacoglossan is a poecilogonic species, and its lagoon populations show a greater reproductive output than Mediterranean populations; they produce a greater number of egg masses and embyros per individual, and the capsules have a wider diameter

"Quand j’avais 7 ans je mai tué " puis je suis devenu schizophrène"

International audiencePsychotic dccompensation can bc perceived as family bonds being attac-ked. It can be limited to a traumatic event like the news of a ncw-born's death or an unbearable crime committed by a child. Parents then give up investing in their child who then goes through a narcissistic "fracture". The authors show from a case study, how this overall disillusion process can bring about paranoid expériences in life.La décompensation psychotique peut être appréhendée comme une attaque des liens familiaux. Elle peut être reliée à un événement traumatique tel l'annonce de la mort d'un nouveau-né ou d'un acte intolérable commis par un enfant. Les parents désinvestissent l'enfant qui vit une "fracture" narcis-sique. Les auteurs montrent à partir d'un cas clinique, comment ce mouve-ment de désillusion massif peut déclencher des vécus paranoïdes

Development of a portable leaf photosynthesis and volatile organic compounds emission system.

Understanding how plant carbon metabolism responds to environmental variables such as light is central to understanding ecosystem carbon cycling and the production of food, biofuels, and biomaterials. Here, we couple a portable leaf photosynthesis system to an autosampler for volatile organic compounds (VOCs) to enable field observations of net photosynthesis simultaneously with emissions of VOCs as a function of light. Following sample collection, VOCs are analyzed using automated thermal desorption-gas chromatograph-mass spectrometry (TD-GC-MS). An example is presented from a banana plant in the central Amazon with a focus on the response of photosynthesis and the emissions of eight individual monoterpenes to light intensity. Our observations reveal that banana leaf emissions represent a 1.1 +/- 0.1% loss of photosynthesis by carbon. Monoterpene emissions from banana are dominated by trans-β-ocimene, which accounts for up to 57% of total monoterpene emissions at high light. We conclude that the developed system is ideal for the identification and quantification of VOC emissions from leaves in parallel with CO2 and water fluxes.The system therefore permits the analysis of biological and environmental sensitivities of carbon metabolism in leaves in remote field locations, resulting in the emission of hydrocarbons to the atmosphere.•A field-portable system is developed for the identification and quantification of VOCs from leaves in parallel with leaf physiological measurements including photosynthesis and transpiration.•The system will enable the characterization of carbon and energy allocation to the biosynthesis and emission of VOCs linked with photosynthesis (e.g. isoprene and monoterpenes) and their biological and environmental sensitivities (e.g. light, temperature, CO2).•Allow the development of more accurate mechanistic global VOC emission models linked with photosynthesis, improving our ability to predict how forests will respond to climate change. It is our hope that the presented system will contribute with critical data towards these goals across Earth's diverse tropical forests

Thermal properties of metal-metal bonded Pd(I) complexes supported onto porous Vycor glass

Thermal behavior of the complexes Pd2(dppm)2Cl2, Pd2(dppm)2(SnCl3)Cl and Pd2(dppm)2(SnCl3)2 (dppm = bis[diphenylphosphino(methane)], ((C6H5)2PCH2P(C6H5)2) in the solid state and immobilized onto porous Vycor glass was studied. Similar decomposition mechanisms were observed for the solid and immobilized complexes, with a small thermal stabilization upon immobilization. The decomposition products were characterized by X-ray diffractometry, Raman and diffuse reflectance infrared spectroscopy, which indicated the presence of a mixture of metallic palladium and oxidized species such as PdO,condensed phosphates, SnO2 and SnP2O7. According to X-ray diffractometry, the decomposition products of the immobilized complexes presented higher amounts of PdO than the solid-state residues, probably as an effect of interactions with silanol groups present in the glass surface.Estudos dos complexos Pd2(dppm)2Cl2, Pd2(dppm)(SnCl3)Cl e Pd2(dppm)2(SnCl3) (dppm = bis[diphenylphosphino(methane)], (C6H5)2PCH2P(C6H5)2) por análise termogravimétrica (TG), no estado sólido e imobilizados no vidro poroso Vycor, são descritos. Os mecanismos de decomposição dos complexos no estado sólido e imobilizados no vidro poroso Vycor são similares e apenas uma ligeira estabilização é observada mediante a imobilização. Os produtos de decomposição foram caracterizados por difração de raios-X, espectroscopias Raman e de Refletância difusa no infravermelho, indicando a presença de uma mistura de paládio metálico e espécies oxidadas tais como PdO, fosfatos condensados, SnO2 e SnP2O7. Os produtos de decomposição dos complexos imobilizados no PVG apresentaram quantidades mais elevadas de PdO do que os resíduos no estado sólido, segundo a difração de raios-X, em virtude provavelmente da ocorrência de reações com grupamentos da superfície do vidro, bem como pelo fato de que as moléculas adsorvidas se encontram isoladas umas em relação às outras.263269Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP

Thermal Properties Of Metal-metal Bonded Pd(i) Complexes Supported Onto Porous Vycor Glass.

Thermal behavior of the complexes Pd2(dppm)2Cl2, Pd2(dppm)2(SnCl3)Cl and Pd2(dppm)2(SnCl3)2 (dppm=bis[diphenylphosphino(methane)], ((C6H5)2PCH2P(C6H5)2) in the solid state and immobilized onto porous Vycor glass was studied. Similar decomposition mechanisms were observed for the solid and immobilized complexes, with a small thermal stabilization upon immobilization. The decomposition products were characterized by X-ray diffractometry, Raman and diffuse reflectance infrared spectroscopy, which indicated the presence of a mixture of metallic palladium and oxidized species such as PdO,condensed phosphates, SnO2 and SnP2O7. According to X-ray diffractometry, the decomposition products of the immobilized complexes presented higher amounts of PdO than the solid-state residues, probably as an effect of interactions with silanol groups present in the glass surface.80263-

Relation between renal calcium content and renal impairment in 246 human renal biopsies

Relation between renal calcium content and renal impairment in 246 human renal biopsies. Tissue calcium content from 246 diagnostic human renal biopsies was measured to assess whether elevated tissue calcium concentration could be demonstrated to exist early during the course of human renal disease or was only a manifestation of advanced renal impairment. Renal calcium content correlated significantly with serum creatinine (r = +0.23, P < 0.001, N = 246); serum phosphate (r = +0.27, P < 0.001, N = 169) but not with serum calcium (r = -0.10, P > 0.1, N = 193). Fivefold greater calcium content was measured in biopsied patients with normal renal function than in normal postmortem renal tissue (35.7 ± 5.2 vs. 7.6 ± 0.7 mgCa/100 g wet renal tissue, P < 0.001). Those biopsied patients with significant functional impairment (SCr > 1.5 mg/dl) had a higher mean level of serum phosphorus and serum [Ca] × [P] product than patients with normal renal function (5.19 ± 0.22 vs. 3.92 ± 0.11mg P/dl and 44.8 ± 1.8 vs. 35.7 ± 1.2 mg2/dl2, respectively), and slightly higher renal calcium content (85.3 ± 32.2 vs. 35.7 ± 5.2 Ca/100 g wet renal tissue, P = 0.06), which correlated with histologic calcium deposition (r = +0.52, P < 0.02, N = 20). These findings are consistent with the hypothesis that renal calcium deposition begins early in the course of a variety of renal diseases and hence may play a secondary pathogenetic role that accelerates progression to chronic renal failure. Severity of renal calcium deposition is equally closely related to hyperphosphatemia and to the level of renal impairment