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.     

New petrified forest in Maranhão,Permian (Cisuralian) of the Parnaíba Basin,Brazil

This work presents a new fossil plant-bearing area located in the municipalities of Duque Bacelar and Coelho Neto, Maranhão State, Brazil, recovered from lower Permian (Cisuralian) strata of the Pedra de Fogo Formation, northeastern portion of the Parnaíba Basin. The area comprises more than five exposures with assemblages formed mostly of large gymnosperm woods, a number of them in life-position (reaching up to ∼2.30 m in height and 1.15 m in diameter) and, in lesser degree, of horizontal tree-fern stems (up to 5 m in length), some of them being referable to Psaronius sp. The fossils are recorded in sedimentary beds of continental origin that accumulated in shallow, nearshore areas of large lakes, which eventually were affected by rapid burial episodes generated by non-channelized, high energy fluvial systems. The new fossil assemblages are included within lacustrine rocks placed at the base of the Pedra de Fogo Formation, i.e., Sílex Basal Member, near the contact with the underlying Piauí Formation (Pennsylvanian). This observation contrasts with previous studies at the southwestern portion of the basin, where the stratigraphic position of plant fossils is referred to the upper Pedra de Fogo Formation (Trisidela Member) or even to the overlying Motuca Formation. The new sites currently suffer damage from human activities and require urgent actions in order to protect them. Based on the current laws, some measures of protection for these sites are discussed and proposed herein.     

Paleoproterozoic migmatitic gneisses from the Tandilia belt (Argentina), Río de la Plata craton,record cooling at deep crustal levels

We studied high-grade metamorphic rocks of the El Cristo hill area of the Tandilia belt. Mineral analyses and thermodynamic calculations were carried out for two adjacent rock samples: an amphibole–biotite gneiss and a garnet–biotite-bearing migmatite. Peritectic garnets in the migmatite show core compositions of pyr_4.5(gro + andr)₁₀spes₆alm_79.5 changing to pyr_3.5(gro + andr)₁₇spes₆alm_73.5 at their thin rims. Garnet compositions in the gneiss are pyr_6.5(gro + andr)₂₆spes₁₂alm_55.5 and pyr_4.5(gro + andr)₃₄spes₁₂alm_49.5 for core and rim, respectively. A P–T path was constructed by calculating pseudosections in the 11-component system Si–Ti–Al–Fe–Mn–Mg–Ca–Na–K–O–H and contouring them by isopleths for garnet components using the PERPLE_X software package. Supra-solidus crystallization of garnet cores in the migmatite began at 5.8 kbar and 660 °C. Garnet rims equilibrated at 7.0 kbar and 640 °C compatible with garnet cores in the amphibole–biotite gneiss (7.6 kbar and 660 °C). The further chemical development of garnet in this rock points to P–T conditions of 11.6 kbar and 620 °C and 12.2 kbar and 595 °C (outermost garnet rim). At this high-pressure stage Ca-amphibole was not stable. Most biotite formed during exhumation whereas the high-pressure accessory minerals, titanite and epidote, persisted. According to the obtained anti-clockwise P–T path the originally partly melted material was tectonically transported from ∼22 km (middle crust) to ∼40 km (lower crust) depths reaching a geothermal gradient as low as 15 °C km⁻¹. This transport probably occurred along a major suture zone, which was active during the Paleoproterozoic (2.25–2.10 Ga), before a terminating collision of terranes near the SW boundary of the Rio de la Plata craton.     

Shear zone evolution and timing of deformation in the Neoproterozoic transpressional Dom Feliciano Belt,Uruguay

New structural, microstructural and geochronological (U-Pb LA-ICP-MS, Ar/Ar, K-Ar, Rb-Sr) data were obtained for the Dom Feliciano Belt in Uruguay. The main phase of crustal shortening, metamorphism and associated exhumation is recorded between 630 and 600 Ma. This stage is related to the collision of the Río de la Plata and Congo cratons at ca. 630 Ma, which also involved crustal reworking of minor crustal blocks such as the Nico Pérez Terrane and voluminous post-collisional magmatism. Subsequent orogen-parallel sinistral shearing gave rise to further deformation up to ca. 584 Ma and resulted from the onset of the convergence of the Kalahari Craton and the Río de la Plata-Congo cratons. Sinistral shear zones underwent progressive strain localization and retrograde conditions of deformation during crustal exhumation. Dextral ENE-striking shear zones were subsequently active at ca. 550 Ma, coeval with further sinistral shearing along N- to NNE-striking shear zones. The tectonothermal evolution of the Dom Feliciano Belt thus recorded the collision of the Río de la Plata and Congo cratons, which comprised one of the first amalgamated nuclei of Gondwana, and the subsequent incorporation of the Kalahari Craton into Western Gondwana.     

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.     

Synchronous deposition of massive sulphide deposits in the Iberian Pyrite Belt: New data from Las Herrerías and La Torerera ore-bodies

Two small to medium sized massive sulphide deposits, Las Herrerías and La Torerera, located in the Iberian Pyrite Belt (IPB) are examined from a geological and palynostratigraphic perspective. The palynological assemblages are assignable to the Retispora lepidophyta–Verrucosisporites nitidus (LN) miospore Biozone (Latest Devonian: Latest Famennian/Strunian) of Western Europe. This age permits correlation with some of the main massive sulphide deposits dated so far in the region (viz., Tharsis, Aznalcóllar, Sotiel-Coronada or Neves-Corvo), and validates once again the hypothesis that a single mineralizing event was responsible for the genesis of most of the IPB’s massive sulphide deposits. The present study confirms that palynostratigraphy is an invaluable high-resolution biostratigraphic tool in the IPB, applicable to dating, correlation and ore-exploration.     

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).     

基于水资源可持续利用的流域产业结构分析

本文以官厅水库流域为例，从宏观经济学角度出发，将流域水资源利用中存在的污染、浪费问题与产业结构的合理性结合起来进行研究。首次采用Fuzzy分析模型对流域产业结构进行分析，据此按发展的适宜性对流域产业进行排序；探讨了导致流域水资源利用问题的深层原因在于产业结构不合理。根据流域现状，提出了产业结构的调整方案，为流域可持续发展决策提供了依据。     

德日进与中国旧石器时代考古学的早期发展

德日进是中国旧石器时代考古学的开拓者与奠基人之一.他与桑志华发现并发掘了水洞沟和萨拉乌苏遗址,参与了关于中国史前考古的第一本专著<中国旧石器时代>的写作.他作为中国地质调查所新生代研究室的顾问参与和指导了周口店遗址的发掘和研究工作,对确认北京猿人石器的人工属性和用火遗迹起过重要的作用,与裴文中一道对周口店的石器工业进行了系统研究,奠定了中国旧石器时代考古学的基础,并与杨钟健等一起建立了周口店遗址的地层层序和地质时代框架.他对中国旧石器时代考古的第一代学人裴文中和贾兰坡有过多方面的指导和帮助,进而对中国旧石器时代考古学的后续发展产生了深远的影响.