Observation of color-transparency in diffractive dissociation of pions

We have studied the diffractive dissociation into dijets of 500 GeV/c pions scattering coherently from carbon and platinum targets. Extrapolating to asymptotically high energies (where t(min)-->0), we find that when the per-nucleus cross section for this process is parametrized as sigma = sigma0Aalpha, alpha has values near 1.6, the exact result depending on jet transverse momentum. These values are in agreement with those predicted by theoretical calculations of color-transparency.     

Direct measurement of the pion valence-quark momentum distribution, the pion light-cone wave function squared

We present the first direct measurements of the pion valence-quark momentum distribution which is related to the square of the pion light-cone wave function. The measurements were carried out using data on diffractive dissociation of 500 GeV/c pi(-) into dijets from a platinum target at Fermilab experiment E791. The results show that the /q&q> light-cone asymptotic wave function describes the data well for Q2 approximately 10 (GeV/c)(2) or more. We also measured the transverse momentum distribution of the diffractive dijets.     

What are the relative roles of heating and cooling in generating solar wind temperature anisotropies?

Temperature anisotropy in the solar wind results from a combination of mechanisms of anisotropic heating (e.g., cyclotron-resonant heating and dissipation of kinetic Alfvén waves) and cooling (e.g., Chew-Goldberger-Low double-adiabatic expansion). In contrast, anisotropy-driven instabilities such as the cyclotron, mirror, and firehose instabilities limit the allowable departure of the plasma from isotropy. This study used data from the Faraday cups on the Wind spacecraft to examine scalar temperature and temperature components of protons. Plasma unstable to the mirror or firehose instability was found to be about 3-4 times hotter than stable plasma. Since anisotropy-driven instabilities are not understood to heat the plasma, these results suggest that heating processes are more effective than cooling processes at creating and maintaining proton temperature anisotropy in the solar wind.     

Coating thickness measurements on gas-borne nanoparticles by combined mobility and aerodynamic spectrometry

An on-line method is described and validated to measure the thickness of coatings on gas-borne nanoparticles. The method is essentially a tandem technique which measures the aerodynamic diameter of a particle twice—before and after coating—by a single-stage low-pressure impactor (SS-LPI) for the same mobility equivalent diameter preselected via differential mobility analyzer (DMA). A shell thickness is then derived from the change in effective particle density determined by the SS-LPI. The method requires a difference in mass density between carrier particle and coating material. Its theoretical sensitivity is shown to range between about 0.1 and 1 nm, depending on the density ratio. One advantage of this approach is that both DMA and SS-LPI are situated in series but downstream of the coating step, so as not to interfere with the coating process. The method was validated against transmission electron microscopy (TEM) measurements, using spherical silica–titania particles coated with conformal shells of molybdenum and bismuth oxide by chemical vapor deposition (CVD). For such spherical particles, the agreement with TEM was excellent. The technique was able to provide layer thicknesses for sub-nanometer layers barely or not resolved by TEM. The paper also discusses the impact of ‘non-ideal’ phenomena such as the formation of doublet particles by coagulation, the effect of multiply charged particles, or the onset of homogeneous decomposition of the coating precursor. With supporting experimental data, it is shown that such phenomena can be interpreted reliably from certain features of the impactor penetration curve. The on-line method can thus be used for fast screening of process parameters and reliable process monitoring for gas-phase synthesis of composite nanopowders.     

High-performance liquid chromatographic determination of chitin in the snow crab, Chionoecetes opilio

A HPLC method was developed for the determination of glucosamine in crab shells. The amount of glucosamine residue can be used to estimate the amount of chitin in analyzed material. Crab samples were hydrolysed with 6M HCl at 100 degrees C for 13 h and the released glucosamine was determined by HPLC using refractive index (RI) detection. Separations were performed using an ODS-2 column with an isocratic mobile phase consisting of 10% methanol, 90% hexanesulfonate, pH 2.1. Glucosamine identification was carried out not only on basis of retention time, but also with respect to mass spectra, which were acquired by HPLC-MS.     

Feldgleichungen der TREDERschen Gravitationstheorie,die aus einem Variationsprinzip ableitbar sind. I

In the frame work of TREDER 's gravitational theory we consider two classes of field equations which are derivable from two classes of LAGRANGE ian densities Ω⁽¹⁾(ω₁, ω₂), Ω⁽²⁾(s?₁, s?₂). ω₁, ω₂; s?₁, s?₂ are parameters. Ω⁽²⁾(ω₁, ω₂) gives us field equations which are up to the post-NEWTON ian approximation in the sense of NORDTVEDT , THORNE and WILL equivalent to the field equations given by BRANS and DICKE . For ω₂ = ?1 ?2ω₁ field equations follow from Ω⁽¹⁾(ω₁, ?1 ?2ω₁) which are in the above mentioned sense of post-NEWTON ian approximation equivalent to EINSTEIN 's equations. The field equations following from Ω⁽¹⁾(ω₁, ω₂) have a cosmological model with the well known cosmological singularities for T → ± ∞ in case that ω₁/(1 +3ω₁ +ω₂) ? γ > 0. For ω₁/(1 +3ω₁ +ω₂) ≤ 0 cosmological models with no cosmological singularities exist. From Ω⁽²⁾(s?₁, s?₂) we obtain field equations which at the best give us perihelion rotation 7% above EINSTEIN 's value and light deflection 7% below the corresponding EINSTEIN 's value. But in that case we are able to show the existence of a cosmological model without any cosmological singularity.     

Sensitive biomonitoring of phthalate metabolites in human urine using packed capillary column switching liquid chromatography coupled to electrospray ionization ion-trap mass spectrometry

A rapid and sensitive method for the determination of the phthalate monoesters monoethyl phthalate (MEP), monobutyl phthalate (MBP), monobenzyl phthalate (MBzP) and monoethylhexyl phthalate (MEHP), in human urine, using packed capillary column liquid chromatography coupled to electrospray quadrupole-ion trap mass spectrometry (ESI-QITMSⁿ) has been developed. Sample volumes of 200 L of deconjugated and diluted urine were loaded onto a precolumn of 30 mm×0.32 mm I.D. packed with Hypercarb 5 m particles, using a sample carrier consisting of acetonitrile/water (15/85, v/v, adjusted to pH 2 using HCl) with a flow rate of 20 L/min. Backflushed elution onto a 100 mm×0.32 mm I.D. analytical column packed with 5 m Hypercarb particles was conducted using a tetrahydrofuran/water gradient where both solvents contained 10 mM ammonium acetate, at a flow rate of 4 L/min. Determination of the monophthalates was achieved within 8 min. Ionization was performed in the negative mode and the analytes were observed as [M-H]^– at m/z=193.1, 221.1, 255.1 and 277.0 for MEP, MBP, MBzP and MEHP, respectively. Quantification was performed in the multiple reaction monitoring (MRM) mode monitoring the fragments at m/z=121.1, 177.0, 183.0 and 233.0 for MEP, MBP, MBzP and MEHP, respectively. The method was validated over the concentration range 2.5–125 ng/mL in pretreated urine samples, corresponding to 25–1250 ng/mL untreated urine, yielding correlation coefficients in the range 0.996–0.999. The within-assay (n=6) and between-assay (n=6) repeatabilities were in the range 4.0–18% and 4.8–15% RSD, respectively. The mass limits of detection were in the range 32–70 pg, corresponding to concentration limits of detection of 1.6–3.5 ng/mL of untreated urine.     

Characterization of the differential protein expression associated with thermoresistance in human gastric carcinoma cell lines

Resistance to chemotherapeutic agents is one of the major problems faced during palliative therapy of tumor cells. Thus, chemotherapy is frequently combined with other modes of therapy such as radiation therapy and/or hyperthermia. Tumor cells respond to heat stress with development of thermotolerance and the interactions between chemo- and thermoresistance phenomena are not clearly understood. In this paper, we analyze the differential protein expression in vitro in human stomach cancer cells, their chemoresistant and thermoresistant counterparts using proteomics. The immediate aim was to identify sets of proteins that may lead to the development of thermoresistance. Based on these results, we aim to develop functional tests and methods for the modulation of thermoresistance and chemoresistance phenomena that may assist the therapy of inoperable cancers.