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Published Values (published + value)
Selected AbstractsA non-main-sequence secondary in SY CancriMONTHLY NOTICES OF THE ROYAL ASTRONOMICAL SOCIETY, Issue 1 2005Robert Connon Smith ABSTRACT Simultaneous spectroscopic and photometric observations of the Z Cam type dwarf nova SY Cancri were used to obtain absolute flux calibrations. A comparison of the photometric calibration with a wide-slit spectrophotometric calibration showed that either method is equally satisfactory. A radial velocity study of the secondary star, made using the far-red Na i doublet, yielded a semi-amplitude of K2= 127 ± 23 km s,1. Taking the published value of 86 ± 9 km s,1 for K1 gives a mass ratio of q=M2/M1= 0.68 ± 0.14; this is very different from the value of 1.13 ± 0.35 quoted in the literature. Using the new lower mass ratio, and constraining the mass of the white dwarf to be within reasonable limits, then leads to a mass for the secondary star that is substantially less than would be expected for its orbital period if it satisfied a main-sequence mass,radius relationship. We find a spectral type of M0 that is consistent with that expected for a main-sequence star of the low mass we have found. However, in order to fill its Roche lobe, the secondary must be significantly larger than a main-sequence star of that mass and spectral type. The secondary is definitely not a normal main-sequence star. [source] U-Pb Age Determination for Seven Standard Zircons using Inductively Coupled Plasma,Mass Spectrometry Coupled with Frequency Quintupled Nd-YAG (, = 213 nm) Laser Ablation System: Comparison with LA-ICP-MS Zircon Analyses with a NIST Glass Reference MaterialRESOURCE GEOLOGY, Issue 2 2008Yuji Orihashi Abstract This paper evaluates the analytical precision, accuracy and long-term reliability of the U-Pb age data obtained using inductively coupled plasma,mass spectrometry (ICP-MS) with a frequency quintupled Nd-YAG (, = 213nm) laser ablation system. The U-Pb age data for seven standard zircons of various ages, from 28 Ma to 2400 Ma (FCT, SL13, 91500, AS3, FC1, QGNG and PMA7) were obtained with an ablation pit size of 30 ,m diameter. For 207Pb/206Pb ratio measurement, the mean isotopic ratio obtained on National Institute of Standards and Technology (NIST) SRM610 over 4 months was 0.9105 ± 0.0014 (n = 280, 95% confidence), which agrees well with the published value of 0.9096. The time-profile of Pb/U ratios during single spot ablation showed no significant difference in shape from NIST SRM610 and 91500 zircon standards. These results encouraged the use of the glass standard as a calibration standard for the Pb/U ratio determination for zircons with shorter wavelength (, = 213 nm) laser ablation. But 206Pb/238U and 207Pb/235U ages obtained by this method for seven zircon standards are systematically younger than the published U-Pb ages obtained by both isotope dilution,thermal ionization mass spectrometry (ID-TIMS) and sensitive high-resolution ion-microprobe (SHRIMP). Greater discrepancies (3,4% younger ages) were found for the 206Pb/238U ages for SL13, AS3 and 91500 zircons. The origin of the differences could be heterogeneity in Pb/U ratio on SRM610 between the different disks, but a matrix effect accuracy either in the ICP ion source or in the ablation-transport processes of the sample aerosols cannot be neglected. When the 206Pb/238U (= 0.2302) newly defined in the present study is used, the measured 206Pb/238U and 207Pb/235U ages for the seven zircon standards are in good agreement with those from ID-TIMS and SHRIMP within ±2%. This suggests that SRM610 glass standard is suitable for ICP-MS with laser ablation sampling (LA-ICP-MS) zircon analysis, but it is necessary to determine the correction factor for 206Pb/238U by measuring several zircon standards in individual laboratories. [source] Echocardiographic Left Ventricular Mass in a Multiethnic Southeast Asian Population: Proposed New Gender and Age-Specific NormsECHOCARDIOGRAPHY, Issue 8 2008M.R.C.P., Raymond Ching-Chiew Wong M.B.B.S. Background: Left ventricular mass (LVM) is an independent risk factor for cardiovascular outcome. We aimed to define normal reference values of LVM/body surface area (BSA) in a multiethnic Southeast Asian population across ages, and define demographic parameters that predict LVM/BSA. Methods: 198 subjects (44% men, mean age 40 ± 14 years, 82% Chinese, 13% Malay and 5% Indian) with no cardiovascular comorbidity and had normal echo images for age were included in the analysis. Echo LVM was calculated as: 1.04 ×[(left ventricular internal diameter at end-diastole {LVIDd}+ interventricular septal thickness at end-diastole {IVSd}+ left ventricular posterior wall thickness at end-diastole {LVPWd})3, LVIDd3× 0.8]+ 0.61, indexed by BSA (LVM/BSA)* and expressed as g/m2. Results: BSA and blood pressure (BP) were comparable between dichotomous age groups < or , 50 years within the same gender. Women aged , 50 years had larger IVSD, LVPWd, LVM and LVM/BSA compared to younger cohort. (p < 0.01 for all variables). The 95th percentile of LVM in men and women were 189 g and 148 g respectively; corresponding values for LVM/BSA were 106 and 96 g/m2. These values are consistently smaller than published values from the West. Age (r = 0.27, P < 0.001), gender (r =,0.30, P < 0.001), and systolic BP (r = 0.25, P = 0.003) were significant univariate predictors of LVM/BSA. Conclusion: We therefore propose a different cutoff value for the diagnosis of LV hypertrophy among Southeast Asians. [source] Environmental factors affecting the levels of legacy pesticides in the airshed of Delaware and Chesapeake Bays, USAENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 9 2010Anubha Goel Abstract Organochlorine insecticides and their degradation products contribute to toxicity in Chesapeake Bay, USA, sediments and affect the reproductive health of avian species in the region; however, little is known of atmospheric sources or temporal trends in concentrations of these chemicals. Weekly air (n,=,265) and daily rain samples (n,=,494) were collected over 2000 to 2003 from three locations in the Delmarva Peninsula, USA. Pesticides were consistently present in the gas phase with infrequent detection in the particle phase. Hexachlorocyclohexanes (HCHs) and cis - and trans -chlordane were detected most frequently (95,100%), and cis - and trans -nonachlor, oxychlordane, heptachlor, heptachlor epoxide, dieldrin, and 1-chloro-4-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene (4,4,-DDE) were also detected frequently. The highest mean air concentrations were for dieldrin (60,84,pg/m3), ,-HCH (37,83,pg/m3), and 4,4,-DDE (16,80,pg/m3). Multiple regression analyses of air concentrations with temperature and wind conditions using modified Clausius-Clapeyron equations explained only 30 to 60% of the variability in concentration for most chemicals. Comparison of the air concentrations and enthalpy of air,surface exchange values at the three sites indicate sources of chlordanes and ,-HCH sources are primarily from long-range transport. However, examination of chlordane isomer ratios indicates some local and regional contributions, and ,-HCH, 4,4,-DDE, dieldrin, heptachlor, heptachlor epoxide, and oxychlordane also have local or regional sources, possibly from contaminated soils. Median rain sample volumes of 1 to 3 L led to infrequent detections in rain; however, average measured concentrations were 2 to 10 times higher than in the Great Lakes. Dissipation half-lives in air were well below 10 years for all chemicals and below published values for the Great Lakes except dieldrin, which did not decline during the sample period. Environ. Toxicol. Chem. 2010;29:1893,1906. © 2010 SETAC [source] Estimating metabolic biotransformation rates in fish from laboratory dataENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 2 2008Jon A. Arnot Abstract A method is proposed for estimating metabolic biotransformation rate constants for nonionic organic chemicals from measured laboratory bioconcentration and dietary bioaccumulation data in fish. Data have been selected based on a quality review to reduce uncertainty in the measured values. A kinetic mass balance model is used to estimate rates of chemical uptake and elimination. Biotransformation rate constants are essentially calculated as the difference between two quantities, a measured bio-concentration factor or elimination rate constant, and a model-derived bioconcentration factor or elimination rate constant estimated assuming no biotransformation. Model parameterization exploits key empirical data when they are available and assumes default values when study specific data are unavailable. Uncertainty analyses provide screening level assessments for confidence in the biotransformation rate constant estimates. The uncertainty analyses include the range for 95% of the predicted values and 95% confidence intervals for the calculated biotransformation values. Case studies are provided to illustrate the calculation and uncertainty methods. Biotransformation rate constants calculated by the proposed method are compared with other published estimates for 31 chemicals that range in octanol,water partition coefficients from approximately 101 to 108 and represent over four orders of magnitude in biotransformation potential. The comparison of previously published values with those calculated by the proposed method shows general agreement with 82% of the estimated values falling within a factor of three. [source] Measurement of Henry's law constant for methyl tert -butyl ether using solid-phase microextractionENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 8 2001Britta G. Bierwagen Abstract Increasing groundwater contamination with methyl tert -butyl ether (MTBE) requires more efficient remediation technologies. Accurate measurement of MTBE's air,water partitioning coefficient (Henry's law constant, H) is important for the design and optimization of removal efficiency for many treatment systems as well as for predicting its fate and transport. Previously published data for MTBE appear to have some unusual nonlinearity at lower temperatures (15,30°C), and a wide range of values exists for dimensionless H at 25°C, from 0.0216 to 0.1226 in the published literature. We measured H for MTBE using headspace solid-phase microextraction (SPME) and a static method that considers equilibrium partitioning in a closed system, for temperatures between 15 and 40°C. To validate our methods, we measured H for benzene, toluene, and trichloroethylene and compared our results to previously published values, with excellent agreement. The Arrhenius plot for MTBE indicates that ln(HMBTE) = 6.85,2,900 T,1, with T in K. At 25°C, HMBTE = 0.0555 ± 0.0122. [source] Phytoplankton production and growth rate in Lake Tanganyika: evidence of a decline in primary productivity in recent decadesFRESHWATER BIOLOGY, Issue 11 2007STEPHANE STENUITE Summary 1. This study focused on phytoplankton production in Lake Tanganyika. We provide new estimates of daily and annual primary production, as well as growth rates of phytoplankton, and we compare them with values published in former studies. 2. Chlorophyll- a (chl- a) in the mixed layer ranged from 5 to 120 mg chl- a m,2 and varied significantly between rainy and dry seasons. Particulate organic carbon concentrations were significantly higher in the south basin (with 196 and 166 mg C m,3 in the dry and the rainy season, respectively) than in the north basin (112 and 109 mg C m,3, respectively). 3. Carbon : phosphorus (C : P) ratios varied according to season. Phosphorus limitation seemed to occur more frequently than nitrogen limitation, especially during the rainy season. Severe P deficiencies were rare. 4. Measured particulate daily primary production ranged from 110 to 1410 mg C m,2 day,1; seasonal contrasts were well marked in the north basin, but less in the south basin, where primary production peaks occurred also in the rainy season. Estimates of annual primary production, based on daily primary production calculated from chl- a and water transparency, gave values lower than those reported in previous studies. Picophytoplankton accounted on average for 56% of total particulate production in the south basin during the wet season of 2003. 5. Phytoplankton growth rates, calculated from primary production, ranged from 0.055 to 0.282 day,1; these are lower than previously published values for Lake Tanganyika. [source] Simultaneous Determination of Fluorine, Chlorine, Bromine and Iodine in Six Geochemical Reference Materials Using Pyrohydrolysis, Ion Chromatography and Inductively Coupled Plasma-Mass SpectrometryGEOSTANDARDS & GEOANALYTICAL RESEARCH, Issue 4 2009Hélène Balcone-Boissard halogènes; pyrohydrolyse; chromatographie ionique; spectrométrie de masse couplée à une source de plasma induit; matériaux géologiques de référence Concentrations of halogens (fluorine, chlorine, bromine and iodine) were determined in six geochemical reference materials (BHVO-2, GS-N, JG-1, JR-1, JB-1b, JB-2). Halogens were first extracted from powdered samples using a pyrohydrolysis technique, then hydrolysis solutions were analysed by ion chromatography for F and Cl and inductively coupled plasma-mass spectrometry for Br and I. The detection limits in solutions were 100 ,g l,1 for both F and Cl and 10 ng l,1 for Br and I. Considering the extraction procedure, performed on a maximum of 500 mg of sample and producing 100 ml of pyrohydrolysis solution, detection limits in rock samples were 20 mg kg,1 for F and Cl and 2 ,g kg,1 for Br and I. The mean analytical errors on the studied composition ranges were estimated at 10 mg kg,1 for F and Cl, 100 ,g kg,1 for Br and 25 ,g kg,1 for I. The concentration values, based on repeated (generally > 10) sample analysis, were in good agreement generally with published values and narrowed the mean dispersion around mean values. Large dispersions are discussed in terms of samples heterogeneity and contaminations during sample preparation. Basaltic RMs were found to be more suitable for studies of halogen compositions than differentiated rock material, especially granites , the powders of which were heterogeneous in halogens at the 500 mg level. Les concentrations en halogènes (fluor, chlore, brome et iode) on été déterminées dans 6 matériaux géologiques de référence (BHVO-2, GS-N, JG-1, JR-1, JB-1b, JB-2), distribués par le GSJ, l'USGS et le CRPG. Les halogènes étaient d'abord extraits des échantillons, disponibles sous forme de poudre, par pyrohydrolyse. F et Cl sont ensuite analysés par chromatographie ionique, Br et I par spectrométrie de masse couplée à une source de plasma induit. Les limites de détection sont de 100 ,g l,1 pour F et Cl, et de 10 ng l,1 pour Br et I, respectivement. L'extraction des halogènes était réalisée sur 500 mg de poudre de roche, produisant 100 ml de solution d'extraction. Ainsi, pour les échantillons de roche, les limites de détection étaient de 20 mg kg,1 pour F et Cl, et 2 ,g kg,1 pour Br et I. L'erreur analytique moyenne sur la gamme de concentration étudiée est estimée à 10 mg kg,1 pour F et Cl, 100 ,g kg,1 pour Br et 25 ,g kg,1 pour I. Les valeurs de concentrations données, obtenues par l'analyse répétée (> 10) du même échantillon étaient en accord avec les valeurs reportées dans la littérature. Elles présentent en général une plus faible dispersion autour de la valeur moyenne. Dans le cas d'une importante dispersion des résultats, celle-ci est discutée en terme d'hétérogénéité de l'échantillon analysé et de contamination durant la préparation du matériel de référence. Les échantillons de référence de composition basaltique se révèlent être plus appropriés pour étudier les compositions en halogènes que les matériaux correspondant à des roches différenciées, en particulier des granites dont la distribution en halogènes apparaît hétérogène dans les poudres à l'échelle d'un aliquot de 500 mg. [source] Evaluation of TCE and MTBE in situ Biodegradation: Integrating Stable Isotope, Metabolic Intermediate, and Microbial Lines of EvidenceGROUND WATER MONITORING & REMEDIATION, Issue 4 2007Jennifer R. McKelvie Compound specific isotope analysis (CSIA) was used to investigate biodegradation of trichloroethene (TCE) and methyl tert -butyl ether (MTBE) at contaminated field sites in Alaska and New York State, respectively. At both sites, geochemical conditions and the presence of metabolic intermediates (cis -1-2-dichloroethene and tert -butyl alcohol [TBA]) suggested the potential for biodegradation of TCE and MTBE, respectively. Given that in both cases these metabolic intermediates could also have been present as cocontaminants in the source zone, CSIA was undertaken to evaluate the possibility of in situ biodegradation. At the TCE-contaminated field site in Alaska, ,13C values of TCE in ground water determined in this study showed no evidence of biodegradation (mean ,13C of ,27.0 ± 1.0, for nine wells), and quantitative-polymerase chain reaction analyses of ground water from four wells found no evidence of dechlorinator Dehalococcoides sp. at this site. At the MTBE-contaminated field site in New York, TBA was present in the ground water but was not present in gasoline sampled from underground storage tanks (UST) on-site, suggesting that at this site, TBA was potentially a metabolite of MTBE biodegradation rather than a cocontaminant. However, at all sampling times and locations, ,13C and ,2H values of MTBE in ground water were within range of published values for undegraded MTBE in gasoline. While the occurrence of a small extent of in situ MTBE biodegradation cannot be ruled out, the findings suggest that it is more likely that multiple gasoline spills occurred through time, and while present day USTs do not contain TBA as a cocontaminant, gasoline spilled at the site in the past may have. At both contaminated field sites, CSIA, chemical, and microbiological lines of evidence suggest that biodegradation was not a significant attenuation process. The results of these two studies underscore the need for an integrated approach to site assessment that draws on measurements of metabolic intermediates, analysis of stable isotopes, and microbial evidence to give a reliable assessment of in situ biodegradation at contaminated field sites. [source] Measured concentrations of combustion gases from the use of unvented gas fireplacesINDOOR AIR, Issue 5 2010P. W. Francisco Abstract, Measurements of combustion product concentrations were taken in 30 homes where unvented gas fireplaces were used. Measurements of CO, CO2, NOx, NO2, O2 (depletion), and water vapor were taken at 1-min interval. The analyzers were calibrated with certified calibration gases for each placement and were in operation for 3,4 days at each home. Measured concentrations were compared to published health-based standards and guidelines. The two combustion gases that exceeded published values were NO2 and CO. For NO2, the Health Canada guideline of 250 ppb (1-h average) was exceeded in about 43% of the sample and the World Health Organization (WHO) guideline of 110 ppb (1-h average) was exceeded in 80% of the sample. Carbon monoxide levels exceeded the U.S. EPA 8-h average standard of 9 ppm in 20% of the sample. Moisture problems were not evident in the test homes. An analysis of the distribution of CO showed that the CO is dispersed throughout the home almost immediately upon operation of the fireplace and that the concentrations throughout the home away from the immediate vicinity of the fireplace are 70,80% of the level near the fireplace. Decay analysis of the combustion gases showed that NO was similarly stable to CO and CO2 in the indoor environment but that both NO2 and water vapor were removed from the air at much greater rates. Practical Implications Previous studies on unvented gas fireplaces have made assumptions of how they are operated by users. This article presents the results of field monitoring of 30 unvented gas fireplaces under normal operation, regardless of whether users follow industry recommendations regarding installation, usage patterns, and maintenance. The monitoring found that health-based standards and guidelines were exceeded for CO in 20% of homes and for NO2 in most homes. There were no identified moisture problems in these homes. Nearly, half of the fireplaces were used at least once for longer than 2 h, counter to manufacturers' intended usage as supplemental heating. This demonstrates that given actual usage patterns and compared to current health-based thresholds, these appliances can produce indoor air concentrations considered to be unhealthy to at least sensitive or at-risk individuals. [source] 2D and 3D upper bound solutions for tunnel excavation using ,elastic' flow fieldsINTERNATIONAL JOURNAL FOR NUMERICAL AND ANALYTICAL METHODS IN GEOMECHANICS, Issue 12 2007Assaf Klar Abstract This paper presents 2D and 3D upper bound solutions for the problem of tunnel excavation in soft ground. The solution invokes the use of incompressible flow fields derived from the theory of elasticity and the concept of sinks and sources. Comparison is made with previously published results. For some geometries the current calculation results in lower (better) upper bound values; however, the results were generally close to previously published values. Copyright © 2007 John Wiley & Sons, Ltd. [source] Aseptic Processing of Sweetpotato Purees Using a Continuous Flow Microwave SystemJOURNAL OF FOOD SCIENCE, Issue 9 2005Pablo Coronel ABSTRACT: Sweetpotato purees (SPP) were aseptically processed using a continuous flow microwave system to obtain a shelf-stable product. The dielectric properties of SPP were measured, and the dielectric constant and loss factor were within the range of the published values for fruits and vegetables. Small-scale tests were conducted in a 5-kW microwave unit to determine changes in color and viscosity with different thermal treatments. The results of these tests showed that color values (L*, a*) and viscosity did not change significantly compared with the untreated control. Pilot-scale tests were then conducted in a 60-kW microwave unit where the product was heated to 135 °C and held at that temperature for 30 s. The pilot-scale test produced a shelf-stable product with no detectable microbial count during a 90-d storage period at room temperature. This is the 1st report of aseptically packaged vegetable puree processed by a continuous flow microwave heating system. [source] Measurement of deep gray matter perfusion using a segmented true,fast imaging with steady-state precession (True-FISP) arterial spin-labeling (ASL) method at 3TJOURNAL OF MAGNETIC RESONANCE IMAGING, Issue 6 2009Elan J. Grossman MS Abstract Purpose To study the feasibility of using the MRI technique of segmented true,fast imaging with steady-state precession arterial spin-labeling (True-FISP ASL) for the noninvasive measurement and quantification of local perfusion in cerebral deep gray matter at 3T. Materials and Methods A flow-sensitive alternating inversion-recovery (FAIR) ASL perfusion preparation was used in which the echo-planar imaging (EPI) readout was replaced with a segmented True-FISP data acquisition strategy. The absolute perfusion for six selected regions of deep gray matter (left and right thalamus, putamen, and caudate) were calculated in 11 healthy human subjects (six male, five female; mean age = 35.5 years ± 9.9). Results Preliminary measurements of the average absolute perfusion values at the six selected regions of deep gray matter are in agreement with published values for mean absolute cerebral blood flow (CBF) baselines acquired from healthy volunteers using positron emission tomography (PET). Conclusion Segmented True-FISP ASL is a practical and quantitative technique suitable to measure local tissue perfusion in cerebral deep gray matter at a high spatial resolution without the susceptibility artifacts commonly associated with EPI-based methods of ASL. J. Magn. Reson. Imaging 2009;29:1425,1431. © 2009 Wiley-Liss, Inc. [source] Biased estimates of nonrenal clearanceJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 7 2001Peter H. Hinderling Abstract The goal of the investigation was to critically evaluate published values for oral nonrenal clearance and their postulated dependence on renal function with drugs administered orally to subjects with varying renal function. Derivation of the pertinent equations indicated that the values reported for oral nonrenal clearance tend to systematically overestimate both the true oral and intravenous nonrenal clearances of these drugs. Computations were performed to confirm these findings not only for subjects with normal renal function, but also for patients with renal impairment. The computations evaluated the relevance of bioavailability and renal clearance of a drug for the bias in the estimates of true oral or intravenous nonrenal clearance. The results of the computations showed that the estimates for true oral and intravenous nonrenal clearance derived from oral data exceed systematically the true values in subjects with normal or reduced renal function. Also, a renal function dependent decrease of the true oral or intravenous nonrenal clearance is falsely diagnosed if apparent oral nonrenal clearance values are used for the estimates. The magnitude of bioavailability and renal clearance impact the bias in the estimates derived from oral data. For drugs with predominant renal excretion and small bioavailability the bias is largest. For drugs with predominant nonrenal elimination and large bioavailability the bias is smallest. © 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 90:960,966, 2001 [source] Measurement of spin-lattice relaxation times and chemical exchange rates in multiple-site systems using progressive saturationMAGNETIC RESONANCE IN MEDICINE, Issue 1 2007Craig J. Galbán Abstract A new method for measuring spin-lattice relaxation times and chemical exchange (CE) rate constants in multiple-site exchanging systems is described. The method, chemical exchange and T1 measurement using progressive saturation (CUPS), was applied to determine T1s and analyze phosphorus exchange among phosphocreatine (PCr), ATP, and inorganic phosphate (Pi), mediated by creatine kinase (CK) and ATP synthase, using 31P-MRS. Two-site exchange was analyzed in vitro and in the rat leg, and three-site exchange was analyzed in the rat heart. Data were fitted to a model of progressive saturation incorporating T1 relaxation and CE. For the in vitro system at 8.45T, we found T1(PCr) = 2.86 s and T1(,-ATP) = 1.72 s. For the rat gastrocnemius at 1.9T, we found T1(PCr) = 6.60 s and T1(,-ATP) = 2.06 s. For the rat heart at 9.4T, we found T1(PCr) = 3.35 s, T1(,-ATP) = 0.69 s, and T1(Pi) = 1.83 s. All of these values were within 20% of literature values. Similarly, the determined exchange rates were in the same range as published values. Using simulations, we compared CUPS with transient saturation transfer as a method for measuring T1s and rates. The two methods showed similar sensitivity to noise. We conclude that CUPS is a viable alternative for measuring T1s and CE rates in exchanging systems. Magn Reson Med 58:8,18, 2007. © 2007 Wiley-Liss, Inc. [source] Physical properties of Martian meteorites: Porosity and density measurementsMETEORITICS & PLANETARY SCIENCE, Issue 12 2007Ian M. COULSON These samples represent igneous rocks, much like basalt. As such, many laboratory techniques designed for the study of Earth materials have been applied to these meteorites. Despite numerous studies of Martian meteorites, little data exists on their basic structural characteristics, such as porosity or density, information that is important in interpreting their origin, shock modification, and cosmic ray exposure history. Analysis of these meteorites provides both insight into the various lithologies present as well as the impact history of the planet's surface. We present new data relating to the physical characteristics of twelve Martian meteorites. Porosity was determined via a combination of scanning electron microscope (SEM) imagery/image analysis and helium pycnometry, coupled with a modified Archimedean method for bulk density measurements. Our results show a range in porosity and density values and that porosity tends to increase toward the edge of the sample. Preliminary interpretation of the data demonstrates good agreement between porosity measured at 100× and 300× magnification for the shergottite group, while others exhibit more variability. In comparison with the limited existing data for Martian meteorites we find fairly good agreement, although our porosity values typically lie at the low end of published values. Surprisingly, despite the increased data set, there is little by way of correlation between either porosity or density with parameters such as shock effect or terrestrial residency. Further data collection on additional meteorite samples is required before more definitive statements can be made concerning the validity of these observations. [source] High-throughput quantification of selenium in individual serum proteins from a healthy human population using HPLC on-line with isotope dilution inductively coupled plasma-MSPROTEINS: STRUCTURE, FUNCTION AND BIOINFORMATICS, Issue 19 2010Sophia Letsiou Abstract In this study, a method, based on dual column affinity chromatography hyphenated to isotope dilution inductively coupled plasma,quadrupole MS, was developed for selenium determination in selenoprotein P, glutathione peroxidase, and selenoalbumin in human serum samples from a group of healthy volunteers (n=399). Method improvement was achieved using methanol-enhanced isotope dilution which resulted in improved sensitivity and removal of isobaric interferences. Although no human serum reference materials are currently certified for their selenium species levels, method development was conducted using human serum reference material BCR 637 and 639 as their Se species content has been reported in the previous studies, and thus comparisons were possible. The mean selenium concentrations determined for the 399 healthy volunteer serum samples were 23±10,ng Se mL,1 for glutathione peroxidase, 49±15,ng Se mL,1 for selenoprotein P and 11±4,ng Se mL,1 for selenoalbumin. These values are found to be in close agreement with published values for a limited number of healthy volunteer samples, and to establish baseline Se levels in serum proteins for an apparently healthy group of individuals, thus allowing for subsequent comparisons with respective values determined for groups of individuals with selenium related health issues, as well as assist in the discovery of potential selenium biomarkers. Also, the relationship between Se serum protein levels and some anthropometric characteristics of the volunteer population were investigated. Additionally, further development of the analytical method used in this study was achieved by adding a size exclusion chromatography column after the two affinity columns via a switching valve. This allowed for the separation of small selenium-containing molecules from glutathione peroxidase and thus enhanced the overall confidence in its identification. [source] Salient features in the locomotion of proboscideans revealed via the differential scaling of limb long bonesBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2010VALERY B. KOKSHENEV The standard differential scaling of proportions in limb long bones (length against circumference) was applied to a phylogenetically wide sample of the Proboscidea, Elephantidae and the Asian (Elephas maximus) and African (Loxodonta africana) elephants. In order to investigate allometric patterns in proboscideans and terrestrial mammals with parasagittal limb kinematics, the computed slopes between long bone lengths and circumferences (slenderness exponents) were compared with published values for mammals, and studied within a framework of the theoretical models of long bone scaling under gravity and muscle forces. Limb bone allometry in E. maximus and the Elephantidae is congruent with adaptation to bending and/or torsion induced by muscular forces during fast locomotion, as in other mammals, whereas the limb bones in L. africana appear to be adapted for coping with the compressive forces of gravity. Hindlimb bones are therefore more compliant than forelimb bones, and the resultant limb compliance gradient in extinct and extant elephants, contrasting in sign to that of other mammals, is shown to be a new important locomotory constraint preventing elephants from achieving a full-body aerial phase during fast locomotion. Moreover, the limb bone pattern of African elephants, indicating a noncritical bone stress not increasing with increments in body weight, explains why their mean and maximal body masses are usually above those for Asian elephants. Differences in ecology may be responsible for the subtle differences observed in vivo between African and Asian elephants, but they appear to be more pronounced when revealed via mechanical patterns dictated by limb bone allometry. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100, 16,29. [source] | |||||||||||||||||||||||||