| 1. |
- Adcox, K, et al.
(författare)
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PHENIX detector overview
- 2003
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Ingår i: Nuclear Instruments & Methods in Physics Research. Section A: Accelerators, Spectrometers, Detectors, and Associated Equipment. - 0167-5087. ; 499:2-3, s. 469-479
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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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| 2. |
- Adler, SS, et al.
(författare)
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PHENIX on-line systems
- 2003
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Ingår i: Nuclear Instruments & Methods in Physics Research. Section A: Accelerators, Spectrometers, Detectors, and Associated Equipment. - 0167-5087. ; 499:2-3, s. 560-592
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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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| 3. |
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| 4. |
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| 5. |
- Chierici, Melissa, 1968, et al.
(författare)
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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
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Ingår i: Deep-Sea Research Part Ii-Topical Studies in Oceanography. - : Elsevier BV. - 0967-0645. ; 51:22-24, s. 2773-2787
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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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| 6. |
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| 7. |
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| 8. |
- Squitieri, Ferdinando, et al.
(författare)
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Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course.
- 2003
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Ingår i: Brain. - : Oxford University Press (OUP). - 0006-8950 .- 1460-2156. ; 126:Pt 4, s. 946-55
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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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| 9. |
- Turner, Charlotta, et al.
(författare)
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Lipase-catalyzed reactions in organic and supercritical solvents : Application to fat-soluble vitamin determination in milk powder and infant formula
- 2001
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Ingår i: Enzyme and Microbial Technology. - 0141-0229. ; 29:2-3, s. 111-121
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Tidskriftsartikel (refereegranskat)abstract
- The aim of this study was to thoroughly investigate the possibility of using enzyme catalyzed hydrolysis and alcoholysis of ester bonds in vitamin A and E esters to facilitate their determination in different food formulas. Two vitamin esters, retinyl palmitate and α-tocopheryl acetate were used as model compounds and two food formulas, milk powder and infant formula, were used as model matrices. Six lipase preparations and one esterase preparation were investigated in the solvents di-isopropyl ether, hexane/ethanol and supercritical carbon dioxide containing ethanol. Three of the enzyme preparations, lipases from Candida antarctica (Novozyme 435), Rhizomucor miehei (Lipozyme IM) and Pseudomonas cepacia, showed considerably higher activity toward retinyl palmitate than the other four enzyme preparations. There was no observed activity with α-tocopheryl acetate using any of the enzyme preparations. Novozyme 435 showed highest activity in supercritical fluid and generally larger tolerance to variations of the investigated parameters. Using this enzyme preparation in supercritical carbon dioxide containing 3 vol% ethanol and 0.03 vol% water at 366 bar and 80°C, quantitative conversion of retinyl palmitate to retinol was obtained. These conditions were then used for simultaneous lipase-catalyzed reaction and extraction of vitamin A and E from milk powder and infant formula. The developed supercritical fluid extraction method using immobilized Candida antarctica preparation seems to be more beneficial to the oxidation prone vitamins A and E compared to extraction methodologies based on alkaline saponification, resulting in comparatively higher recoveries.
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| 10. |
- Turner, C, et al.
(författare)
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Supercritical fluid extraction and chromatography for fat-soluble vitamin analysis.
- 2001
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Ingår i: Journal of Chromatography A. - 0021-9673. ; 936:1, s. 37-215
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Tidskriftsartikel (refereegranskat)abstract
- Extraction and chromatographic separation of fat-soluble vitamins is a challenging task, due to the sensitivity of these compounds towards light, oxygen, heat and pH. In light of this, supercritical fluid extraction (SFE) and supercritical fluid chromatography (SFC) are attractive techniques as they function at considerably milder conditions than conventional solvent-based analytical techniques. Moreover, supercritical techniques consume much less amounts of organic solvents than conventional ones. This review gives a brief description of suitable supercritical media as well as basic theory on SFE and SFC processes. Furthermore, guidelines are provided for optimizing the important extraction and separation parameters to facilitate a successful method development. Finally, applications employing SFE and/or SFC for fat-soluble vitamin enrichment and final determination are reviewed.
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