高脂饮食对小鼠脂肪代谢和矿物元素代谢的影响

为探讨高脂饮食对小鼠脂肪代谢和矿物元素代谢的影响,用昆明(KM)小鼠24只,出生28 d后随机分成2组,各12只,分别给予高脂饲料与普通饲料,饲养至第9周眼球取血处死,取皮下、腹腔、肠系膜脂肪,毛,肝,血,计算体质量脂肪质量比,测定毛、肝、血中Zn、Ca、Cu、Mn、Mg、Fe含量。结果表明,高脂饮食小鼠体质量增加(P<0.05),单位腹腔脂肪及血Ch显著性增加(P<0.01)。肝Zn、Cu、Mg、Fe、Mn显著降低(P<0.01),血凝块Zn升高(P<0.05),Cu降低(P<0.05),毛Mg降低(P<0.05)。提示高脂饮食引起体质量与血脂增加,脂肪堆积,矿物元素代谢紊乱;不同器官矿物元素的代谢紊乱有差异,以肝脏最显著。     

The structure, energetics, and nature of the chemical bonding of phenylthiol adsorbed on the Au(111) surface: implications for density-functional calculations of molecular-electronic conduction

The adsorption of phenylthiol on the Au(111) surface is modeled using Perdew and Wang density-functional calculations. Both direct molecular physisorption and dissociative chemisorption via S-H bond cleavage are considered as well as dimerization to form disulfides. For the major observed product, the chemisorbed thiol, an extensive potential-energy surface is produced as a function of both the azimuthal orientation of the adsorbate and the linear translation of the adsorbate through the key fcc, hcp, bridge, and top binding sites. Key structures are characterized, the lowest-energy one being a broad minimum of tilted orientation ranging from the bridge structure halfway towards the fcc one. The vertically oriented threefold binding sites, often assumed to dominate molecular electronics measurements, are identified as transition states at low coverage but become favored in dense monolayers. A similar surface is also produced for chemisorption of phenylthiol on Ag(111); this displays significant qualitative differences, consistent with the qualitatively different observed structures for thiol chemisorption on Ag and Au. Full contours of the minimum potential energy as a function of sulfur translation over the crystal face are described, from which the barrier to diffusion is deduced to be 5.8 kcal mol(-1), indicating that the potential-energy surface has low corrugation. The calculated bond lengths, adsorbate charge and spin density, and the density of electronic states all indicate that, at all sulfur locations, the adsorbate can be regarded as a thiyl species that forms a net single covalent bond to the surface of strength 31 kcal mol(-1). No detectable thiolate character is predicted, however, contrary to experimental results for alkyl thiols that indicate up to 20%-30% thiolate involvement. This effect is attributed to the asymptotic-potential error of all modern density functionals that becomes manifest through a 3-4 eV error in the lineup of the adsorbate and substrate bands. Significant implications are described for density-functional calculations of through-molecule electron transport in molecular electronics.     

ABO_3，A_2BO_4型复合氧化物催化剂用于CO，CH_4，NH_3完全氧

本文探讨了ＣＯ，ＣＨ＿４和ＮＨ＿３在ＬａＮｉＯ＿３，Ｌａ＿２ＮｉＯ＿４和ＬａＳｒＮｉＯ＿４三个催化剂上的氧化行为，并得出结论：对于ＣＯ氧化，关键步骤在于ＣＯ在催化剂表面上的络合活化。Ｎｉ￣（３＋）含量越高，越利于ＣＯ的络合活化。对于氨氧化，催化反应遵循氧化－还原机理。Ｎｉ￣（３＋）是主要的活性离子，晶格氧是主要活性氧种。对于ＣＨ＿４氧化，催化机理较复杂，只是发现Ａ＿２ＢＯ＿４型氧化物（Ｌａ＿２ＮｉＯ＿４，ＬａＳｒＮｉＯ＿４）比ＡＢＯ＿３型氧化物（ＬａＮｉＯ＿３）较利于ＣＨ＿４的氧化。     

On the thermodynamics of an ideal fermi gas on the lattice at finite density

We study the ideal gas of fermions on a lattice at finite density for both naive and Wilson fermions. Comparing the thermodynamical quantities thus calculated with the known results in the continuum theory, we are led to propose a modification of the naive form of the lattice action, which is same for both the naive and the Wilson fermions. The thermodynamical quantities, calculated by using this form, are shown to have the correct continuum limit.     

A wave-packet formulation of multiparticle production at high energies

Starting from a free boson gas in a box, we formulate a statistical approach to multi-particle production. The specific feature of the small box quantization is the fact that one-particle wave functions are wave packets instead of plane waves. In this context we investigate the jet model with Bose-Einstein (BE) statistics. The transverse cut-off function is naturally related to the size of the box (production region). We compare our results with experimental data.     

Optimal control of a coefficient in modification Navier-Stokes equations

This paper deals with the optimal control of a coefficient in the modification of Navier-Stokes equations. Namely, the motion of the viscous incompressible fluid for a small gradient of velocity is described by Navier-Stokes equations where the coefficient of the kinematic viscosity ν is the positive constant (ν ₀). For a greater gradient of velocity the coefficient of kinematic viscosity is a positive function of the gradient of velocity, that is ν (|∇u|). In our case ν (|∇u|) = ν ₀ + ν ₁ a (|∇u|) where ν ₀, ν ₁ ∈ ℝ₊. The function a is positive and monotone and it is taken as a control variable. The existence of a solution of the optimal control problem is proved. Further, the approximation of the control problem by the finite-dimensional control problem is performed. The proof of the existence of a solution of that aproximate problem has been brought into light. Finally, the connection between the solution of the control problem and the solution of the approximate control problem is established.     

Asymptotic expressions for remainder terms of some quadrature rules

Asymptotic expressions for remainder terms of the mid-point, trapezoid and Simpson’s rules are given. Corresponding formulas with finite sums are also given.      

Transition from a quark-gluon plasma in the presence of a sharp front

The effect of a sharp front separating the quarkgluon plasma phase from the hadronic phase is investigated. Energy-momentum conservation and baryon number conservation constrain the possible temperature jump across the front. If one assumes that the temperature in the hadronic phase isT200 MeV, as has been suggested by numerous results from relativistic ion collisions, one can determine the corresponding temperature in the quark phase with the help of continuity equations across the front. The calculations reveal that the quark phase must be in a strongly supercooled state. The stability of this solution with respect to minor modifications is investigated. In particular the effect of an admixture of hadronic matter in the quark phase (e.g. in the form of bubbles) is considered in detail. In the absence of admixture the transition proceeds via a detonation transition and is accompanied by a substantial super-cooling of the quark-gluon plasma phase. The detonation is accompanied by less supercooling if a small fraction of bubbles is allowed. By increasing the fraction of bubbles the supercooling becomes weaker and eventually the transition proceeds via a smoother deflagration wave.     

Determination of flavone C-glucosides in antioxidant of bamboo leaves (AOB) fortified foods by reversed-phase high-performance liquid chromatography with ultraviolet diode array detection

A sensitive solid-phase microextraction and gas chromatography-pulsed flame photometric detection technique was developed to quantify volatile sulfur compounds in wine. Eleven sulfur compounds, including hydrogen sulfide, methanethiol, ethanethiol, dimethyl sulfide, diethyl sulfide, methyl thioacetate, dimethyl disulfide, ethyl thioacetate, diethyl disulfide, dimethyl trisulfide and methionol, can be quantified simultaneously by employing three internal standards. Calibration curves were established in a synthetic wine, and linear correlation coefficients (R2) were greater than 0.99 for all target compounds. The quantification limits for most volatile sulfur compounds were 0.5 ppb or lower, except for methionol which had a detection limit of 60 ppb. The recovery was studied in synthetic wine as well as Pinot noir, Cabernet Sauvignon, Pinot Grigio, and Chardonnay wines. Although the sulfur compounds behaved differently depending on the wine matrix, recoveries of greater than 80% were achieved for all sulfur compounds. This technique was applied to analyze volatile sulfur compounds in several commercial wine samples; methionol concentrations were found at the ppm level, while the concentrations for hydrogen sulfide, methanethiol, and methyl thioacetate were at ppb levels. Only trace amounts of disulfides and trisulfides were detected, and ethanethiol was not detected.