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1.
  • Adcox, K, et al. (författare)
  • PHENIX detector overview
  • 2003
  • Ingår i: Nuclear Instruments & Methods in Physics Research. Section A: Accelerators, Spectrometers, Detectors, and Associated Equipment. - 0167-5087. ; 499:2-3, s. 469-479
  • Tidskriftsartikel (refereegranskat)abstract
    • The PHENIX detector is designed to perform a broad study of A-A, p-A, and p-p collisions to investigate nuclear matter under extreme conditions. A wide variety of probes, sensitive to all timescales, are used to study systematic variations with species and energy as well as to measure the spin structure of the nucleon. Designing for the needs of the heavy-ion and polarized-proton programs has produced a detector with unparalleled capabilities. PHENIX measures electron and muon pairs, photons, and hadrons with excellent energy and momentum resolution. The detector consists of a large number of subsystems that are discussed in other papers in this volume. The overall design parameters of the detector are presented. (C) 2002 Elsevier Science B.V. All rights reserved.
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  • Adler, SS, et al. (författare)
  • PHENIX on-line systems
  • 2003
  • Ingår i: Nuclear Instruments & Methods in Physics Research. Section A: Accelerators, Spectrometers, Detectors, and Associated Equipment. - 0167-5087. ; 499:2-3, s. 560-592
  • Tidskriftsartikel (refereegranskat)abstract
    • The PHENIX On-Line system takes signals from the Front End Modules (FEM) on each detector subsystem for the purpose of generating events for physics analysis. Processing of event data begins when the Data Collection Modules (DCM) receive data via fiber-optic links from the FEMs. The DCMs format and zero suppress the data and generate data packets. These packets go to the Event Builders (EvB) that assemble the events in final form. The Level-1 trigger (LVL1) generates a decision for each beam crossing and eliminates uninteresting events. The FEMs carry out all detector processing of the data so that it is delivered to the DCMs using a standard format. The FEMs also provide buffering for LVL1 trigger processing and DCM data collection. This is carried out using an architecture that is pipelined and deadtimeless. All of this is controlled by the Master Timing System (MTS) that distributes the RHIC clocks. A Level-2 trigger (LVL2) gives additional discrimination. A description of the components and operation of the PHENIX On-Line system is given and the solution to a number of electronic infrastructure problems are discussed. (C) 2002 Elsevier Science B.V. All rights reserved.
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5.
  • Mathiasson, Lennart, et al. (författare)
  • Development of methods for the determination of vitamins A, E and beta-carotene in processed foods based on supercritical fluid extraction: a collaborative study.
  • 2002
  • Ingår i: Food Additives and Contaminants. - : Informa UK Limited. - 0265-203X. ; 19:7, s. 632-646
  • Tidskriftsartikel (refereegranskat)abstract
    • New methodologies based on supercritical fluid extraction (SFE) have been developed for the determination of fat-soluble vitamins in processed foods. The results obtained so far indicate that SFE is well suited to extraction of fat-soluble vitamins from food products, although validation work is required to establish accuracy and precision. The vitamins investigated were A, E and beta-carotene, and the processed foods were UHT milk, milk powder, minced meat, liver paste, infant formula, canned baby food and margarine. Extraction equipment employed analyte collection on either a solid-phase trap or in a solvent. After extraction, the samples were saponified and the vitamins determined using reversed-phase liquid chromatography with ultraviolet or fluorescence detection. Sample throughput was at least 12 samples day(-1), i.e. at least twice the number achievable with a conventional extraction methodology. The detection limits for the vitamins in different processed foods were well below 0.1 microg g(-1). Recoveries (in comparison with vitamin levels obtained using conventional solvent extraction) were close to 100% for experienced personal with access to modern automatic equipment. To reach this level, it was necessary to protect the vitamins with an antioxidant during the different steps of the analysis procedure, to add methanol or ethanol to the extraction cell to facilitate the analyte extraction from the food matrix, and when using a solid-phase trap, to employ a fractionated extraction-elution procedure to prevent breakthrough losses. The developed methods were tested in a validation exercise between five laboratories, which had taken part in the method development, and in an intercomparison between 10 laboratories including laboratories with less experience of vitamin determination. The within-laboratory RSD was generally
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8.
  • Chierici, Melissa, 1968, et al. (författare)
  • Variability in pH, fCO(2), oxygen and flux of CO2 in the surface water along a transect in the Atlantic sector of the Southern Ocean
  • 2004
  • Ingår i: Deep-Sea Research Part Ii-Topical Studies in Oceanography. - : Elsevier BV. - 0967-0645. ; 51:22-24, s. 2773-2787
  • Tidskriftsartikel (refereegranskat)abstract
    • Underway sampling and measurements of pH, fCO(2), oxygen and Chlorophyll a (Chl a) were performed in the surface waters from Cape Town (South Africa) to Queen Maud Land (Antarctica) in the Atlantic sector of the Southern Ocean during the austral summer 1997/1998. From direct measurements of these parameters and from calculated fCO(2) the oceanic carbon dioxide system was studied and related to hydrological and biological parameters. fCO(2) was in general undersaturated relative to the atmosphere and showed a large variability with values ranging from 313 to 377 muatm with a mean value of 346 +/- 13 muatm. The undersaturation was more pronounced in areas associated with fronts where high Chl a and high pH in situ values were observed. Using shipboard wind speed data, estimates of the CO2 flux were made along the transect and during three mesoscale surveys on the northward return transect in the area of the Spring Ice Edge (SIE), the Winter Ice Edge (WIE) and in the Antarctic Polar Front (APF). The undersaturation observed during the transect caused the ocean to act as a sink for CO2 with a mean sea-air flux for the entire transect of -3+/-5 mmol m(-2) d(-1) with a large variability between -20 mmol m(-2) d(-1) (oceanic uptake) to 1.3 mmol m(-2) d(-1) (oceanic source). The lowest fCO(2) values (largest oceanic uptake Of COD were found at the southern boundary of the APF at 53degreesS, which coincided with a supersaturation in oxygen and high pH values. Oxygen concentrations were measured from 50degreesS to 63degreesS and varied between 324 and 359 mumol kg(-1) with a mean value of 347 +/- 9 mumol kg(-1). In general only small deviations from equilibrium oxygen saturation were observed (mean value = 99+/-2%). However, in the SIE oxygen was clearly undersaturated, probably an effect of upwelling of oxygen poor deep water which had not yet been compensated for by biological production. Three weeks later, the ice edge had retreated in the SIE region and the Chl a concentration had increased three-fold, suggesting the start of a phytoplankton bloom. This was also seen in the oxygen concentration which had increased and showed supersaturation. This coincided with an increased oceanic uptake of CO2 in the SIE during the mesoscale survey. (C) 2004 Elsevier Ltd. All rights reserved.
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9.
  • Croot, P. L., et al. (författare)
  • The distribution and specification of iron along 6 degrees E in the Southern Ocean
  • 2004
  • Ingår i: Deep-Sea Research Part Ii-Topical Studies in Oceanography. - : Elsevier BV. - 0967-0645. ; 51:22-24, s. 2857-2879
  • Tidskriftsartikel (refereegranskat)abstract
    • The distribution and speciation of iron was determined along a transect in the eastern Atlantic sector (6degreesE) of the Southern Ocean during a collaborative Scandinavian/South African Antarctic cruise conducted in late austral summer (December 1997/January 1998). Elevated concentrations of dissolved iron (>0.4 nM) were found at 60degreesS in the vicinity of the Spring Ice Edge (SIE) in tandem with a phytoplankton bloom, chiefly dominated by Phaeocystis sp. This bloom had developed rapidly after the loss of the seasonal sea ice cover. The iron that fuelled this bloom was mostly likely derived from sea ice melt. In the Winter Ice Edge (WIE), around 55degreesS, dissolved iron concentrations were low (<0.2 nM) and corresponded to lower biological productivity, biomass. In the Antarctic Polar Front, at approximately 50degreesS, a vertical profile of dissolved iron showed low concentrations (<0.2 nM); however, a surface survey showed higher concentrations (1-3 nM), and considerable patchiness in this dynamic frontal region. The chemical speciation of iron was dominated by organic complexation throughout the study region. Organic iron-complexing ligands ([L]) ranged from 0.9 to 3.0 nM Fe equivalents, with complex stability log K'(FeL) = 21.4-23.5. Estimated concentrations of inorganic iron (Fe') ranged from 0.03 to 0.79 pM, with the highest values found in the Phaeocystis bloom in the SIE. A vertical profile of iron-complexing ligands in the WIE showed a maximum consistent with a biological source for ligand production and near surface minimum possibly consistent with loss via photodecomposition. This work further confirms the role iron that has in the Southern Ocean in limiting primary productivity. (C) 2004 Elsevier Ltd. All rights reserved.
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10.
  • Dahlqvist, Ralf, 1973, et al. (författare)
  • Association of calcium with colloidal particles and speciation of calcium in the Kalix and Amazon rivers
  • 2004
  • Ingår i: Geochimica Et Cosmochimica Acta. - : Elsevier BV. - 0016-7037 .- 1872-9533. ; 68:20, s. 4059-4075
  • Tidskriftsartikel (refereegranskat)abstract
    • A considerable amount of colloidally bound Ca has been detected in water samples from Amazonian rivers and the Kalix River, a sub-arctic boreal river. Fractionation experiments using several analytical techniques and processing tools were conducted in order to elucidate the matter. Results show that on average 84% of the total Ca concentration is present as free Ca. Particulate, colloidal and complexed Ca constitute the remaining 16%, of which the colloidal fraction is significant. Ultrafiltration experiments show that the colloidal fraction in the sampled Amazonian rivers and the Kalix River range between 1% and 25%. In both the Amazonian and the Kalix rivers the technique of cross-flow ultrafiltration was used to isolate particles and colloids. The difference in concentration measured with ICP-AES and a Ca ion-selective electrode in identical samples was used to define the free Ca concentration and thus indirectly the magnitude of the particulate, colloidal and complexed fractions. Results from the Kalix and Amazonian rivers are in excellent agreement. Furthermore, the results show that the colloidal concentrations of Ca can be greatly overestimated (up to 227%) when conventional analysis and calculation of ultrafiltration data is used due to retention of free Ca ions during the ultrafiltration process. Calculation methods for colloidal matter are presented in this work, using complementary data from ISE analysis. In the Kalix River temporal changes in the fractionation of Ca were studied before, during and after a spring-flood event. Changes in the size distribution of colloidally associated Ca was studied using FlFFF (Flow Field-Flow Fractionation) coupled on-line to a HR ICP-MS. The FlFFF-HR ICP-MS fractograms clearly show the colloidal component of Ca, supporting the ultrafiltration findings. During winter conditions the size distribution of colloidally associated Ca has a concentration maximum at similar to5 to 10 nm in diameter, shifting to smaller sizes (<5 mm) during and after the spring flood. This shift in size distribution follows a change in the river during this period from ironoxyhydroxy colloids being the most important colloidal carrier phase to humic substances during and after the spring flood. WHAM and NICA-Donnan models were used to calculate the amount of colloidally bound Ca. The results similar for both models, show that on average 16% of the Ca may be associated to a colloidal phase, which is in broad agreement with the measurements. Copyright (C) 2004 Elsevier Ltd.
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12.
  • Kalscheuer, Vera M, et al. (författare)
  • Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation
  • 2003
  • Ingår i: Nature Genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 35:4, s. 313-315
  • Tidskriftsartikel (refereegranskat)abstract
    • We found mutations in the gene PQBP1 in 5 of 29 families with nonsyndromic (MRX) and syndromic (MRXS) forms of X-linked mental retardation (XLMR). Clinical features in affected males include mental retardation, microcephaly, short stature, spastic paraplegia and midline defects. PQBP1 has previously been implicated in the pathogenesis of polyglutamine expansion diseases. Our findings link this gene to XLMR and shed more light on the pathogenesis of this common disorder.
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  • Painter, S., et al. (författare)
  • Effect of heterogeneity on radionuclide retardation in the alluvial aquifer near Yucca Mountain, Nevada
  • 2001
  • Ingår i: Ground Water. - : Wiley. - 0017-467X .- 1745-6584. ; 39:3, s. 326-338
  • Tidskriftsartikel (refereegranskat)abstract
    • The U.S. Department of Energy is currently studying Yucca Mountain, Nevada, as a potential site for a geological high-level waste repository. In the current conceptual models of radionuclide transport at Yucca Mountain, part of the transport path to pumping locations would be through an alluvial aquifer, Interactions with minerals in the alluvium are expected to retard the downstream migration of radionuclides, thereby delaying arrival times and reducing ground water concentrations. We evaluate the effectiveness of the alluvial aquifer as a transport barrier using the stochastic Lagrangian framework. A transport model is developed to account for physical and chemical heterogeneities and rate-limited mass transfer between mobile and immobile zones. The latter process is caused by small-scale heterogeneity and is thought to control the macroscopic-scale retardation in some field experiments. A geostatistical model for the spatially varying sorption parameters is developed from a site-specific database created from hydrochemical measurements and a calibrated modeling approach (Turner and Pabalan 1999). Transport of neptunium is considered as an example. The results are sensitive to the rate of transfer between mobile and immobile zones, and to spatial variability in the hydraulic conductivity. Chemical heterogeneity has only a small effect, as does correlation between hydraulic conductivity and the neptunium distribution coefficient. These results illustrate how general sensitivities can be explored with modest effort within the Lagrangian framework. Such studies complement and guide the application of more detailed numerical simulations.
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15.
  • Painter, S., et al. (författare)
  • Significance of kinetics for sorption on inorganic colloids : Modeling and experiment interpretation issues
  • 2002
  • Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 36:24, s. 5369-5375
  • Tidskriftsartikel (refereegranskat)abstract
    • A two-site kinetic model for solute sorption on inorganic colloids is developed. The model quantifies linear first-order sorption on two types of sites (fast and slow) characterized by two pairs of rates (forward and reverse). We use the model to explore data requirements for long-term predictive calculations of colloid-facilitated transport and to evaluate laboratory kinetic sorption data of Lu et al.. Five batch sorption data sets are considered with plutonium as the tracer and montmorillonite, hematite, silica, and smectite as colloids. Using asymptotic results applicable on the time stale of limited duration experiments, a robust estimation procedure is developed for the fast-site partitioning coefficient K-c and the slow forward rate alpha. The estimated range of K-c is 1.1-76 L/g, and the range for a is 0.0017-0.02 1/h. The fast reverse rate k(r) is estimated in the range 0.012-0.1 1/h. Comparison of one-site and two-site sorption interpretations reveals the difficulty in, discriminating between the two models for montmorillonite and to a lesser extent for hematite. For silica and smectite, the two-site model clearly provides a better representation of the data as compared with a single site model. Kinetic data for silica are available for different colloid concentrations (0.2 g/L and 1 g/L). For the range of experimental conditions considered, a. appears to be independent of colloid concentration.
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16.
  • Sandström, K. J. Mattias, et al. (författare)
  • Multivariate evaluation of factors influencing the performance of a formic acid biosensor for use in air monitoring
  • 2001
  • Ingår i: The Analyst. - : Royal Society of Chemistry. - 0003-2654 .- 1364-5528. ; 126:11, s. 2008-2014
  • Tidskriftsartikel (refereegranskat)abstract
    • A formic acid biosensor for air monitoring has been evaluated using chemometric methods. Using experimental design eleven factors that could influence the performance of the biosensor were examined. The response matrices consisted of six parameters (steady state currents at three different formic acid concentrations and response rates during changes in formic acid concentrations) describing the performance of the biosensor. The data were evaluated using a combination of principal component analysis (PCA) and multiple linear regression (MLR). To confirm the conclusions from the PCA-MLR partial least squares (PLS) was also used. The most important factor for the biosensor performance was found to be the enzyme concentration. Using the information from the chemometric analyses the optimum operation conditions for the biosensor were determined. The steady state currents were increased by 18-30% and the initial two response rates increased by 47-89% compared with a biosensor that had not been optimised.
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17.
  • Squitieri, Ferdinando, et al. (författare)
  • Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course.
  • 2003
  • Ingår i: Brain. - : Oxford University Press (OUP). - 0006-8950 .- 1460-2156. ; 126:Pt 4, s. 946-55
  • Tidskriftsartikel (refereegranskat)abstract
    • Huntington disease is caused by a dominantly transmitted CAG repeat expansion mutation that is believed to confer a toxic gain of function on the mutant protein. Huntington disease patients with two mutant alleles are very rare. In other poly(CAG) diseases such as the dominant ataxias, inheritance of two mutant alleles causes a phenotype more severe than in heterozygotes. In this multicentre study, we sought differences in the disease features between eight homozygotes and 75 heterozygotes for the Huntington disease mutation. We identified subjects homozygous for the Huntington disease mutation by DNA testing and compared their clinical features (age at onset, symptom presentation, disease severity and disease progression) with those of a group of heterozygotes, who were assessed longitudinally. The age at onset of symptoms in the homozygote cases was within the range expected for heterozygotes with the same CAG repeat lengths, whereas homozygotes had a more severe clinical course. The observation of a more rapid decline in motor, cognitive and behavioural symptoms in homozygotes was consistent with the extent of neurodegeneration as available at imaging in three patients, and at the post-mortem neuropathological report in one case. Our analysis suggests that although homozygosity for the Huntington disease mutation does not lower the age at onset of symptoms, it affects the phenotype and the rate of disease progression. These data, once confirmed in a larger series of patients, point to the possibility that the mechanisms underlying age at onset and disease progression in Huntington disease may differ.
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18.
  • Subrahmanyam, S, et al. (författare)
  • Bite-and-switch approach to creatine recognition by use of molecularly imprinted polymers
  • 2000
  • Ingår i: Advanced Materials. - : John Wiley andamp;amp; Sons, Ltd. - 0935-9648 .- 1521-4095. ; 12:10, s. 722-
  • Tidskriftsartikel (refereegranskat)abstract
    • The detection of creatine is important in the analysis of athletes and body builders. Here is reported the preparation of a synthetic polymer using imprinting polymerization, which leaves the polymer with receptor-mimicking recognition sites that are specific for creatine. Molecular recognition results in a fluorescent complex (see Figure) and thus represents a bite-and-switch" mechanism.
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19.
  • Tombelli, S, et al. (författare)
  • Coupling of a DNA piezoelectric biosensor and polymerase chain reaction to detect apolipoprotein E polymorphisms
  • 2000
  • Ingår i: Biosensors & bioelectronics. - : Elsevier Science B.V., Amsterdam.. - 0956-5663 .- 1873-4235. ; 15:08-jul, s. 363-370
  • Tidskriftsartikel (refereegranskat)abstract
    • In this paper we report the coupling of the Polymerase Chain Reaction (PCR) with a piezoelectric biosensor to detect a point mutation in a human gene. Biotinylated 23-mer probes were immobilised on the streptavidin coated gold surface of a quartz crystal; streptavidin was covalently bound to the thiol/dextran modified gold surface. The hybridisation of the immobilised probes with a short sequence (23 mer) complementary, non-complementary and mismatched DNA was investigated: the device was able to distinguish the different synthetic oligonucleotides. Many cycles of measurements can be performed on the same crystal surface regenerating the single strand of DNA with 1 mM of HCl. The same hybridisation reaction was then performed using real samples of human DNA extracted from blood and amplified by PCR, following a standard procedure for genetic detection of the polymorphism of the apolipoprotein E (apoE) gene. The procedure was able to distinguish the sequences present in the different samples, which differ only in one base: in this way it was possible distinguish between different groups of genotypes with apoE typing. Experiments with blank samples confirmed the absence of adsorption or non-specific effects on the quartz crystal treated with the reported procedure. (C) 2000 Elsevier Science S.A. All rights reserved.
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20.
  • Turner, David R., 1951, et al. (författare)
  • The SWEDARP 1997/98 Expedition.
  • 2004
  • Ingår i: Deep Sea Research Part II. ; 51, s. 2543-2879
  • Tidskriftsartikel (refereegranskat)
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21.
  • Turner, David R., 1951, et al. (författare)
  • The SWEDARP 1997/98 marine expedition: overview
  • 2004
  • Ingår i: Deep-Sea Research Part Ii-Topical Studies in Oceanography. - : Elsevier BV. ; 51, s. 2745-2756.
  • Tidskriftsartikel (refereegranskat)abstract
    • The SWEDARP 1997/98 expedition aboard the S.A. Agulhas focused on three study areas along the 6degreesE meridian: 60degreesS, the location of the spring ice edge; 56degreesS, the location of the winter ice edge; and 50.5degreesS, the Antarctic Polar Front. This intensive study was preceded by a north-south transect through the area measuring surface water properties while under way. An extensive measurement programme included hydrography, tracers, nutrients, organic carbon, trace metals, bacteria, and primary and secondary producers (including production and grazing rates). Analysis of the results from the three study areas does not identify a single factor limiting primary production: water column stability and the optical regime, and probably iron supply contributed to the control of primary production. The study area acted as a sink for atmospheric CO2 at the time of measurement, while analysis of water column carbon inventories indicated a net CO2 source integrated over the spring season. (C) 2004 Elsevier Ltd. All rights reserved.
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