Refinement of Phosphorus Determination in Quartz by LA‐ICP‐MS through Defining New Reference Material Values

The aim of this study was to improve the quality of laser ablation inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) determination of phosphorus in crystalline quartz. Over the last decade, the Geological Survey of Norway has routinely performed trace element determinations on quartz from both operating and potential quartz deposits by LA‐ICP‐MS. The determined phosphorus concentrations were, with but few exceptions, consistently within the range of 10 to 30 μg g^?1, results that seemed to be both too high and too consistent. The multi‐material calibration curve obtained from a suite of reference materials (NIST SRM 610, 612, 614, 1830, BAM No. 1 amorphous SiO₂ glass) did not define a precise regression line. Published phosphorus concentrations for the reference materials are poorly constrained and the observed dispersions along the multi‐material calibration curve suggest that some of the reference values may be inaccurate. Furthermore, the calibration curve did not pass through the origin of the [(cps ³¹P/cps ³⁰Si) · cone. Si] vs. P concentration diagram; thus, in addition to the uncertainties of the literature values of phosphorus, it is difficult to define the calibration curve. Three reference materials (NIST SRM 614, 1830, synthetic quartz KORTH) were sent for phosphorus accelerator implantation, providing an independent and accurate (± 3%) approach for determining phosphorus concentrations in crystalline quartz. The intrinsic phosphorus concentrations of the three implanted samples plus those for NIST SRM 610 and 612 were determined by secondary ion mass spectrometry (SIMS), yielding new phosphorus values for NIST SRM 610, 612, 614 and 1830. Using these new values resulted in a better defined LA‐ICP‐MS calibration curve. However, the source of the ICP‐MS related background could not be defined, such that it must still be empirically corrected for.     

Mercury,Trace Elements and Organic Constituents in Atmospheric Fine Particulate Matter,Shenandoah National Park,Virginia, USA: A Combined Approach to Sampling and Analysis

Compliance with U.S. air quality regulatory standards for atmospheric fine particulate matter (PM_2.5) is based on meeting average 24 hour (35 μ m^?3) and yearly (15 μg m^?3) mass‐per‐unit‐volume limits, regardless of PM_2.5 composition. Whereas this presents a workable regulatory framework, information on particle composition is needed to assess the fate and transport of PM_2.5 and determine potential environmental/human health impacts. To address these important non‐regulatory issues an integrated approach is generally used that includes (1) field sampling of atmospheric particulate matter on filter media, using a size‐limiting cyclone, or with no particle‐size limitation; and (2) chemical extraction of exposed filters and analysis of separate particulate‐bound fractions for total mercury, trace elements and organic constituents, utilising different USGS laboratories optimised for quantitative analysis of these substances. This combination of sampling and analysis allowed for a more detailed interpretation of PM_2.5 sources and potential effects, compared to measurements of PM_2.5 abundance alone. Results obtained using this combined approach are presented for a 2006 air sampling campaign in Shenandoah National Park (Virginia, USA) to assess sources of atmospheric contaminants and their potential impact on air quality in the Park. PM_2.5 was collected at two sampling sites (Big Meadows and Pinnacles) separated by 13.6 km. At both sites, element concentrations in PM₂₅ were low, consistent with remote or rural locations. However, element/Zr crustal abundance enrichment factors greater than 10, indicating anthropogenic input, were found for Hg, Se, S, Sb, Cd, Pb, Mo, Zn and Cu, listed in decreasing order of enrichment. Principal component analysis showed that four element associations accounted for 84% of the PM_2.5 trace element variation; these associations are interpreted to represent: (1) crustal sources (Al, REE); (2) coal combustion (Se, Sb), (3) metal production and/or mobile sources (Mo, Cd, Pb, Cu, Zn) and (4) a transient marine source (Sr, Mg). Concentrations of Hg in PM_2.5 at background levels in the single pg m^?3 were shown by collection and analysis of PM_2.5 on filters and by an automated speciation analyser set up at the Big Meadows air quality site. The speciation unit revealed periodic elevation of reactive gaseous mercury (RGM) that co‐occurred with peaks in SO₂, indicating an anthropogenic source. GC/MS total ion current chromatograms for the two sites were quite similar indicating that organic signatures were regional in extent and/or that the same compounds were present locally at each site. Calculated carbon preference index values for n‐alkanes indicated that plant waxes rather than anthropogenic sources, were the dominant alkane source. Polycyclic aromatic hydrocarbons (PAHs) were detected, with a predominance of non‐alkylated, and higher molecular weight PAHs in this fraction, suggestive of a combustion source (fossil fuel or forest fires).     

The Preparation of Marine Geological Certified Reference Materials - Polymetallic Nodule GSPN-1 and Marine Sediment GSMS-1 from the Central Pacific Ocean*

This report describes the location, collection, preparation, homogeneity testing, analysis, data-processing and assignment of certified values of a polymetallic nodule (GSPN-1) and marine sediment (GSMS-1). Materials used in the preparation of these reference materials were collected in 1986 and 1987 from the central Pacific Ocean, by the Chinese Ministry of Geology and Mineral Resources (MGMR). A total of fifty one recommended element concentrations and five proposed concentrations are reported for GSPN-1. For GSMS-1, a total of fifty recommended and seven proposed values are presented.     

雁列断层变形过程中的声发射特征

对拉张型、挤压型雁列断层变形过程中岩桥区和主断层上的声发射特征进行了对比研究，结果表明，雁列断层变形中的声发射对应着多种机制：拉张型雁列岩桥区的声发射为单一事件组成，波振幅小、持续时间短、主频高、震源机制为张裂型；挤压型雁列岩桥区的声发射也是单一事件，波振幅较大、持续时间短、主频较低、震源机制为双剪型；而雁列主干断层上的声发射由多事件组成，波振幅大、持续时间长、主频低、震源机制与挤压型雁列岩桥区的声发射机制不同。这些特点与各区域所处力学状态有关     

Zinc Isotopic Compositions of NIST SRM 683 and Whole‐Rock Reference Materials

In this study the homogeneity of the zinc isotopic composition in the NIST SRM 683 reference material was examined by measuring the Zn isotopic signature in microdrilled sample powders from two metal nuggets. Zinc was purified using AG MP‐1M resin and then measured by MC‐ICP‐MS. Instrumental mass bias was corrected using the “sample‐standard bracketing” method and empirical external normalisation with Cu doping. After evaluating the potential effects of varying acid mass fractions and different matrices, high‐precision Zn isotope data were obtained with an intermediate measurement precision better than ± 0.05‰ (δ⁶⁶Zn, 2s) over a period of 5 months. The δ⁶⁶Zn_JMC‐Lyon mean values of eighty‐four and fourteen drilled powders from two nuggets were 0.11 ± 0.02‰ and 0.12 ± 0.02‰, respectively, indicating that NIST SRM 683 is a good isotopic reference material with homogeneous Zn isotopes. The Zn isotopic compositions of seventeen rock reference materials were also determined, and their δ⁶⁶Zn values were in agreement with most previously published data within 2s. The δ⁶⁶Zn values of most of the rock reference materials analysed were in the range 0.22–0.36‰, except for GSP‐2 (1.07 ± 0.06‰, n = 12), NOD‐A‐1 (0.96 ± 0.03‰, n = 6) and NOD‐P‐1 (0.78 ± 0.03‰, n = 6). These comprehensive data should serve as reference values for quality assurance and interlaboratory calibration exercises.     

Forty‐Nine Major and Trace Element Concentrations Measured in Soil Reference Materials NIST SRM 2586, 2587, 2709a, 2710a and 2711a Using ICP‐MS and Wavelength Dispersive‐XRF

Excellent agreement was noted in the concentration of major and trace elements in five NIST (National Institute for Science and Technology) soil reference materials (NIST SRM 2586, 2587, 2709a, 2710a and 2711a) between measurement results from wavelength dispersive‐XRF and ICP‐MS from two independent laboratories, and NIST certificate of analysis and literature data. We describe the variability in concentrations of up to forty‐nine elements (plus loss on ignition) and provide values for up to twenty‐one elements previously uncharacterised by NIST in these soil RMs. The additional characterisation provided in this investigation can be utilised to reduce the measurement bias of custom calibration routines and improve the quality of control checks developed using these NIST RMs.     

A synthesis: Late Cenozoic stress field distribution at northeastern corner of the Eastern Mediterranean,SE Turkey

Fault kinematic analysis and inversion of focal mechanisms of shallow earthquakes reveal significant evolution of the regional stress regime in the northeastern most corner of the Eastern Mediterranean region since the Mio-Pliocene to the present time. This study was carried out in the interaction area between the Arabian/African plates and the Anatolian block. The evolution of stress regimes consists of a change from older transpression to younger transtension. Both strike-slip stress regimes having a NNW- to northwest-trending σ_Hmax (σ₁) and ENE- to northeast-trending σ_Hmin (σ₃) axes induce a sinistral component of displacement on the major intra-continental Karatas–Osmaniye and Misis–Ceyhan faults elongated with the northeast-trending Misis Range between Adana and Osmaniye provinces (sub-area i) and by a NNE-trending plate boundary Amanos fault running along Amanos Range between Antakya and Kahramanmaras provinces (sub-area ii). The inversion results show that the transtensional stress regime is dominantly strike-slip to extension, with an ENE- to northeast-trending σ_Hmin (σ₃) axis for sub-areas (i) and (ii), respectively. The inversions of earthquake focal mechanisms indicate that the transtensional stress regime is still active in the whole study area since probably recent Quaternary time. To cite this article: S. Over et al., C. R. Geoscience 336 (2004).     

Mesures in situ par infiltrométrie des propriétés hydrodynamiques des sols de Mnasra (Maroc)

The aim of this work is the field hydraulic characterisation of Mnasra soils in northern Morocco, which represents an essential step to study the hydraulic and chemical transports through the vadose zone. We have used a tension infiltrometer associated with a transient axisymmetric infiltration method to determine the hydraulic conductivity, which reduces the duration of measurements. This allows us to characterise a large area with many measurements. Parameters of the characteristic functions K(h) and θ(h) are estimated for six different soils belonging to two geomorphologically different domains: a sandy zone and an alluvial plain. To cite this article: K. Tamoh, A. Maslouhi, C. R. Geoscience 336 (2004).     

Determination of Incompatible Trace Elements in Mantle Clinopyroxenes by LA-ICP-MS: A Comparison of Analytical Performance with Established Techniques

Incompatible trace element abundances have been determined in mantle-derived clinopyroxenes by laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) in a comparative study with established microanalytical and bulk techniques. Individual clinopyroxene grains were sampled for the laser ablation study from sieved mineral separate fractions, from which similar mineral grains had been previously extracted for microprobe (SIMS) and bulk (INAA and ID-TIMS) analysis. Mineral grains were ablated with variable degrees of surface spatial resolution (50-200 μm) in order to maximise ICP-MS analyte count rates and to improve detection limits. A comparison of results from the different techniques reveals that for the most homogeneous samples LA-ICP-MS can achieve excellent levels of agreement with other techniques (10%) and good precision for most of the studied elements (1-5% RSD). Variations in calculated concentrations by LA-ICP-MS confirm inter- and intra-mineral heterogeneity determined by SIMS, reflecting changes in sample composition and texture. The long-term reproducibility of the technique is shown by the consistency of results for one sample analysed on thirteen occasions over a period of nine months.     

Uber,Public Transit,and Urban Transportation Equity: A Case Study in New York City

With the explosive growth of Uber and other mobility service providers, their influences on urban mobility have attracted attention from both researchers and policy circles alike, yet few quantitative studies have been conducted on the topic. Using Uber pickup data in New York City in 2014, this article investigates the spatiotemporal relationship between Uber and public transit using buffer analysis and spatial cross-correlation analysis and assesses Uber’s impact on urban transportation equity with the Gini coefficient and correlation analysis. Our results confirm previous arguments that Uber both complements and competes with public transit, but competition is more prevalent in New York City. Specifically, Uber competes with public transit during most hours of the day and in areas with good public transit coverage, whereas it complements public transit at midnight and in places with insufficient public transit services. The distribution of Uber services is highly unequal, and Uber’s role in improving transport equity is insignificant. Correlation analysis shows that there tend to be fewer Uber pickups in low-income areas, which diverges from previous studies suggesting that Uber serves low-income areas well. In addition, a weak negative correlation is detected between the number of Uber pickups and the percentage of minorities.