Rare earth and other trace element mobility during mylonitization: a comparison of the Brevard and Hope Valley shear zones in the Appalachian Mountains, USA

In progressing from a granitoid mylonite to an ultramylonite in the Brevard shear zone in North Carolina, Ca and LOI (H₂O) increase, Si, Mg, K, Na, Ba, Sr, Ta, Cs and Th decrease, while changes in Al, Ti, Fe, P, Sc, Rb, REE, Hf, Cr and U are relatively small. A volume loss of 44% is calculated for the Brevard ultramylonite relative to an Al–Ti–Fe isocon. The increase in Ca and LOI is related to a large increase in retrograde epidote and muscovite in the ultramylonite, the decreases in K, Na, Si, Ba and Sr reflect the destruction of feldspars, and the decrease in Mg is related to the destruction of biotite during mylonitization. In an amphibolite facies fault zone separating grey and pink granitic gneisses in the Hope Valley shear zone in New England, compositional similarity suggests the ultramylonite is composed chiefly of the pink gneisses. Utilizing an Al–Ti–Fe isocon for the pink gneisses, Sc, Cr, Hf, Ta, U, Th and M-HREE are relatively unchanged, Si, LOI, K, Mg, Rb, Cs and Ba are enriched, and Ca, Na, P, Sr and LREE are lost during deformation. In contrast to the Brevard mylonite, the Hope Valley mylonite appears to have increased in volume by about 70%, chiefly in response to an introduction of quartz. Chondrite-normalized REE patterns of granitoids from both shear zones are LREE-enriched and have prominent negative Eu anomalies. Although REE increase in abundance in the Brevard ultramylonites (reflecting the volume loss), the shape of the REE pattern remains unchanged. In contrast, REE and especially LREE decrease in abundance with increasing deformation of the Hope Valley gneisses. Mass balance calculations indicate that ≥95% of the REE in the Brevard rocks reside in titanite. In contrast, in the Hope Valley rocks only 15–40% of the REE can be accounted for collectively by titanite, apatite and zircon. Possible sites for the remaining REE are allanite, fluorite or grain boundaries. Loss of LREE from the pink gneisses during deformation may have resulted from decreases in allanite and perhaps apatite or by leaching ofy REE from grain boundaries by fluids moving through the shear zone. Among the element ratios most resistant to change during mylonitization in the Brevard shear zone are La/Yb, Eu/Eu*, Sm/Nd, La/Sc, Th/Sc, Th/Yb, Cr/Th, Th/U and Hf/Ta, whereas the most stable ratios in the Hope Valley shear zone are K/Rb, Rb/Cs, Th/U, Eu/Eu*, Th/Sc, Th/Yb, Sm/Nd, Th/Ta, Hf/Ta and Hf/Yb. However, until more trace element data are available from other shear zones, these ratios should not be used alone to identify protoliths of deformed rocks.     

Pleistocene and Holocene aeolian facies along the Huelva coast (southern Spain): climatic and neotectonic implications

The stratigraphic relationships, genesis and chronology, including radiocarbon dating, of the Quaternary sandy deposits forming the El Asperillo cliffs (Huelva) were studied with special emphasis on the influence of neotectonic activity, sea-level changes and climate upon the evolution of the coastal zone. The E-W trending normal fault of Torre del Loro separates two tectonic blocks. The oldest deposits occur in the upthrown block. They are Early to Middle Pleistocene fluviatile deposits, probably Late Pleistocene shallow-marine deposits along an E-W trending shoreline, and Late Pleistocene and Holocene aeolian sands deposited under prevailing southerly winds. Three Pleistocene and Holocene aeolian units accumulated in the downthrown block. Of these, Unit 1, is separated from the overlying Unit 2 by a supersurface that represents the end of the Last Interglacial. Accumulation of Unit 2 took place during the Last Glacial under more arid conditions than Unit 1. The supersurface separating Units 2 and 3 was formed between the Last Glacial maximum at 18 000 ¹⁴C yr BP and ca. 14 000 ¹⁴C yr BP, the latter age corresponding to an acceleration of the rise of sea level. Unit 3 records wet conditions. The supersurface separating Units 3 and 4 fossilised the fault and the two fault blocks. Units 4 (deposited before the 4th millennium BC), 5 (> 2700 ¹⁴C yr BP to 16th century) and 6 (16th century to present) record relatively arid conditions. Prevailing wind directions changed with time from W (Units 2–4) to WSW (Unit 5) and SW (Unit 6).     

LA-ICP-MS study of apatite- and K feldspar-hosted primary carbonatite melt inclusions in clinopyroxenite xenoliths from lamprophyres, Hungary: Implications for significance of carbonatite melts in the Earth’s mantle

We report the results of LA-ICP-MS analyses of rock forming minerals in clinopyroxene-apatite-K feldspar-phlogopite (CAKP) metasomatic xenoliths and primary carbonatite melt inclusions (CMI) hosted in apatite (Ap) and K feldspar (Kfs). The xenoliths are from the Cretaceous lamprophyre dikes of the Transdanubian Central Range, Hungary. The CMI in Ap have phosphorus dolomitic composition as opposed to CMI in Kfs, which display dolomitic alkali-aluminosiliceous character. The melts found in CMI in Ap and in Kfs likely formed by liquid-liquid separation from an originally carbonate- and phosphorous-rich melt. Primitive mantle (PM) normalized trace element distributions of both Ap- and Kfs-hosted CMI (n = 60 and 20, respectively) reveal a strong negative Ti-anomaly, and an extreme enrichment in incompatible elements (U, Th, LILE and LREE) relative to HREE, Sc, V, Ni and Cr. Rarely, apatites contain unique CMI, which show major- and trace-element signature transitional to K feldspar-hosted CMI. This is due to heterogeneous entrapment of an immiscible phosphorous-bearing carbonatite melt and a carbonate-bearing alkali aluminosiliceous melt, which is a further evidence for their co-existence. CMI reveal that U, Th, Pb, Nb, Ta, P, Sr, Y and REE partitioned into the phosphorous-bearing carbonatite melt, whereas Cs, Rb, Na, K, B, Al, Zr and Hf preferred the silicate-bearing liquid.PM normalized REE pattern (high LREE/HREE), elevated Zr and Hf contents and negative Ti anomaly of clinopyroxene (Cpx) indicate that its formation is genetically linked to carbonatite metasomatism attested by CMI. Trace element partitioning between the studied Cpx and CMI is in accordance with experimentally determined trace element distributions between Cpx and carbonatite melt. Cpx, which occur in samples with high modal proportion of apatite represent mantle section, which interacted with a higher amount of “initial” carbonatite melt than Cpx from apatite-poor xenoliths. This is confirmed by higher Cr, Ni, V, Sc, Ti and lower Zr, as well as Hf concentration in Cpx from xenoliths with low modal abundance of Ap. CMI reveal that Ti, V, Ni and Cr were in lower concentration in the “initial” carbonatite melt than in PM. Contrarily, Zr and Hf were more abundant in this melt than in PM. Consequently, a continuously migrating “initial” carbonatite melt, increased Zr and Hf concentration, and decreased Ti, Sc, V, Ni and especially Cr in the clinopyroxenes. Our findings suggest that the studied CAKP rocks were formed by carbonatite melt metasomatism, which occurred in an open system in the upper mantle.     

Petrology and geochemistry of prograde deserpentinized peridotites from Happo-O’ne, Japan: Evidence of element mobility during deserpentinization

The prograde deserpentinized peridotites from the talc zone in the Happo-O’ne complex, central Japan, show differences in their field relation and mineral assemblage with the high-P retrograde peridotites of the other part of the complex. They show a mineral assemblage, olivine + talc + antigorite ± prograde tremolite ± chlorite, formed by thermal metamorphism around the granitic intrusion at T, 500-650 °C and P < 7 kbar. The olivine has numerous opaque inclusions and high Fo (91.5-96.5) relative to the retrograde olivine, reflecting its formation by deserpentinization. The prograde tremolite, which is low in Al₂O₃ (<1.0 wt.%), Cr₂O₃ (<0.35 wt.%), and Na₂O (<0.6 wt.%) but high in Mg# (up to 0.98) and SiO₂ (up to 59.9 wt.%), is different in size, shape and chemistry from the retrograde tremolite. The prograde peridotites display a U-shaped REE pattern (0.02-0.5 times PM), similar to diopside-zone retrograde metaperidotites, possible protoliths. They are enriched in LILE (e.g., Cs, Pb, Sr, Rb) relative to HFSE (e.g., Ta, Hf, Zr, Nb), like their protoliths, because of their local re-equilibration with the fluid released during dehydration of the protoliths. They have high contents of REE and some trace elements (e.g., Cs, Th, U, Ta) relative to their protoliths because of an external-element addition from the granitic magma. In-situ analyses of peridotitic silicates confirmed that the prograde tremolite and talc display a spoon-shaped primitive mantle (PM)-normalized REE pattern (0.1-3 times PM) in which LREE are higher than HREE contents. The prograde tremolite is depleted in Al, Na, Cr, Sc, V, Ti, B, HREE and Li, but is enriched in Si, Cs, U, Th, HFSE (Hf, Zr, Nb, Ta), Rb and Ba relative to the retrograde tremolite; the immobile-element depletion in this tremolite is inherited from its source (antigorite + secondary diopside), whereas the depletion of mobile elements (e.g., Li, B, Na, Al) is ascribed to their mobility during the deserpentinization and/or the depleted character of the source of tremolite. The enrichment of HFSE and LILE in the prograde tremolite is related to an external addition of these elements from fluid/melt of the surrounding granitic magma and/or in situ equilibrium with LILE-bearing fluid released during dehydration of serpentinized retrograde metaperidotites and olivine-bearing serpentinites (protoliths). The prograde olivine is higher in REE and most trace-element contents than the retrograde one due to the external addition of these elements; it is enriched in B, Co and Ni, but depleted in Li that was liberated during deserpentinization by prograde metamorphism.     

Compositional characteristics of wolframite in tin deposits,Dupangling, Guangxi

Statistical data on major, trace and rare-earth elements in wolframite from the quartz vein-and greisen-type tin deposits in the Dupangling orefield reveal: (1) The components in wolframite can be divided into two relatively independent groups: the WO₃-Nb-Ta-Sc-REE group, in which WO₃ is negatively correlated with the others and the FeO-MnO-Sn group, in which MnO is negatively correlated with the other two; (2) In general, REE fractionation is not significant, reflected mainly by the separation of Eu from other REE’s. LREE and HREE increase or decrease simultaneously, with HREE being more variable; (3) Nb, Ta, Sc, REE substitute for W, and Sn may enter into wolframite lattice accompanied by Fe-Mn substitution; (4) In contrast to wolframite in quartz veins, which is poor in REE, Nb, Ta and Sc and has highδ Eu values and LREE / HREE and Nb/Ta ratios, wolframite in greisen is rich in REE, Nb, Ta, Sc and has lowδ Eu values and LREE/HREE and Nb/Ta ratios; and (5) The contents and ratios of trace elements and REE partitioning parameters of wolframite can be used as guide for prospecting.     

Neutron Activation Analysis Applied to the Determination of Heavy Metals and Other Trace Elements in Sediments from Sepetiba Bay (RJ), Brazil

In this work, instrumental neutron activation analysis (INAA) was applied to the determination of the elements As, Ba, Br, Ce, Co, Cr, Cs, Eu, Fe, Hf, La, Lu, Nd, Rb, Sc, Sm, Ta, Tb, Th, U, Yb, Zn in twenty eight bottom sediment samples from Sepetiba Bay, Rio de Janeiro, Brazil. With the concentration data obtained, contour maps were prepared, by using Kriging method, to show the spatial distribution of the studied elements in the Bay. The elements Co, Cr, Cs, Fe, Sc, Ta and Zn showed similar behaviour in the sediments, with higher concentrations along the northern coast of the bay, where the fluvial water inputs are concentrated. The distribution of U, rare earth elements and Ba in the Bay indicates that these elements are not deposited as contaminants.     

相山两种不同成因角闪石的地球化学特征对比

通过详细研究相山两种不同成因角闪石的元素及同位素地球化学发现：江西相山铀矿田北部同时存在两种不同成因的角闪石：正变质成因的角闪石，寄主岩石为斜长角闪(片)岩，微量元素以富集大离子亲石元素(LILE)(K,Rb，Th，Ta，U)、稍为富集Ti,Se和相对贫高场强元素(HFSE)(Zr，Hf,Y，Yb，Cr，HREE)为特征，稀土总量低，稀土分布型式为近水平型，δ^18O为7．95～8．58，显示变质火成岩的氧同位素特征；副变质成因的角闪石，寄主岩石为含石榴角闪石英片岩．微量元素以高度富集大离子亲石元素(LILE)(K，Rb，Th，U)、稍为富集Ta,Nb，Ce，Zr，Hf，Sm和相对贫高场强元素(HFSE)(Ti，Y，Yb，Cr)、强烈亏损Sc为特征，稀土总量高．轻重稀土相互分离程度高，轻稀土富集，O同位素组成(δ^18O)较高，为9．95～10．02，显示碎屑沉积变质岩的氧同位素特征。     

Heterogeneous mantle source and magma differentiation of quaternary arc-like volcanic rocks from Tengchong,SE margin of the Tibetan Plateau

The Tengchong volcanic field north of the Burma arc comprises numerous Quaternary volcanoes in the southeastern margin of the Tibetan Plateau. The volcanic rocks are grouped into four units (1–4) from the oldest to youngest. Units 1, 3 and 4 are composed of olivine trachybasalt, basaltic trachyandesite and trachyandesite, and Unit 2 consists of hornblende dacite. The rocks of Units 1, 3, and 4 form a generally alkaline suite in which the rocks plot along generally linear trends on Harker diagrams with only slight offset from unit to unit. They contain olivine phenocrysts with Fo values ranging from 65 to 85 mol% and have Cr-spinel with Cr# ranging from 23 to 35. All the rocks have chondrite-normalized REE patterns enriched in LREE and primitive mantle-normalized trace element patterns depleted in Ti, Nb and Ta, but they are rich in Th, Ti and P relative to typical arc volcanics. Despite minor crustal contamination, ⁸⁷Sr/⁸⁶Sr ratios (0.706–0.709), εNd values (−3.2 to −8.7), and εHf values (+4.8 to −6.4) indicate a highly heterogeneous mantle source. The Pb isotopic ratios of the lavas (²⁰⁶Pb/²⁰⁴Pb = 18.02–18.30) clearly show an EMI-type mantle source. The underlying mantle source was previously modified by subduction of the Neo-Tethyan oceanic and Indian continental lithosphere. The present heterogeneous mantle source is interpreted to have formed by variable additions of fluids and sediments derived from the subducted Indian Oceanic lithosphere, probably the Ninety East Ridge. Magma generation and emplacement was facilitated by transtensional NS-trending strike-slip faulting.     

Mineralogical and chemical changes of soil and stream sediment formed by intense weathering of the Danburg granite, Georgia, U.S.A.

A series of soil and stream sediments developed during intense weathering on the metaluminous Danburg granite, northeastern Georgia, U.S.A., have been analyzed mineralogically and chemically. The concentrations of Ba, Na, Rb and Cs in the silt and coarser fractions are controlled mainly by feldspars and biotite. Hf is controlled by zircon, and the REE (rare-earth elements) and Th are largely controlled by sphene. Variations in feldspar, sphene and zircon may produce small variations in Eu/Sm and La/Lu ratios. Ferromagnesian minerals control Ta, Fe, Co, Sc and Cr concentrations.

The mineralogical and chemical composition of the Danburg granite is more closely reflected in the silt than in the sand or gravel fractions of stream sediments. In the silt, the contents of Rb, REE, Th, Ta, Fe, Co and Sc and the ratios of La/Sc, Th/Sc, La/Co, Th/Co, Eu/Sm and La/Lu are similar to those in the unweathered granite. In contrast, these element contents or ratios in the sands and gravels are 0.05−3× the concentration in the unweathered granite. Ta and Ba contents are an exception to the above. The Ta and Ba contents of the sands and gravels are similar to those of the granite.

In the kaolinite-halloysite clays, the content of Na is depleted relative to the source. Rb, Cs, Ba, Hf and Ta are depleted or enriched in the clays relative to the source, while the REE, Th, Fe, Co, Sc and Cr are enriched. The Eu/Sm (Eu anomaly size) and La/Lu ratios, and the REE patterns of the clays are similar to those of the source.

Thus, the mineralogy and element contents of a siltstone developed from metaluminous, granitic sources during intense weathering would be expected to be more similar to the source rock than the sandstones and conglomerates. Claystones should contain similar REE patterns and Eu/Sm ratios as the source rock, but such fine-grained sediments might represent much larger areas of source rocks than the more locally derived sandstones or conglomerates.     

In situ analyses of micas in the Yashan granite,South China: Constraints on magmatic and hydrothermal evolutions of W and Ta–Nb bearing granites

Most rare-metal granites in South China host major W deposits with few or without Ta–Nb mineralization. However, the Yashan granitic pluton, located in the Yichun area of western Jiangxi province, South China, hosts a major Nb–Ta deposit with minor W mineralization. It is thus important for understanding the diversity of W and Nb–Ta mineralization associated with rare-metal granites. The Yashan pluton consists of multi-stage intrusive units, including the protolithionite (-muscovite) granite, Li-mica granite and topaz–lepidolite granite from the early to late stages. Bulk-rock REE contents and La/Yb ratios decrease from protolithionite granite to Li-mica granite to topaz–lepidolite granite, suggesting the dominant plagioclase fractionation. This variation, together with increasing Li, Rb, Cs and Ta but decreasing Nb/Ta and Zr/Hf ratios, is consistent with the magmatic evolution. In the Yashan pluton, micas are protolithionite, muscovite, Li-mica and lepidolite, and zircons show wide concentration ranges of ZrO₂, HfO₂, UO₂, ThO₂, Y₂O₃ and P₂O₅. Compositional variations of minerals, such as increasing F, Rb and Li in mica and increasing Hf, U and P in zircon are also in concert with the magmatic evolution from protolithionite granite to Li-mica granite to topaz–lepidolite granite. The most evolved topaz–lepidolite granite has the highest bulk-rock Li, Rb, Cs, F and P contents, consistent with the highest contents of these elements and the lowest Nb/Ta ratio in mica and the lowest Zr/Hf ratio in zircon. Ta–Nb enrichment was closely related to the enrichment of volatile elements (i.e. Li, F and P) in the melt during magmatic evolution, which raised the proportion of non-bridging oxygens (NBOs) in the melt. The rims of zoned micas in the Li-mica and topaz–lepidolite granites contain lower Rb, Cs, Nb and Ta and much lower F and W than the cores and/or mantles, indicating an exotic aqueous fluid during hydrothermal evolution. Some columbite-group minerals may have formed from exotic aqueous fluids which were originally depleted in F, Rb, Cs, Nb, Ta and W, but such fluids were not responsible for Ta–Nb enrichment in the Yashan granite. The interaction of hydrothermal fluids with previously existing micas may have played an important role in leaching, concentrating and transporting W, Fe and Ti. Ta–Nb enrichment was associated with highly evolved magmas, but W mineralization is closely related to hydrothermal fluid. Thus these magmatic and hydrothermal processes explain the diversity of W and Ta–Nb mineralizations in the rare-metal granites.     

酸性矿山排水影响的水库沉积物微量元素地球化学特征

为了解酸性矿山排水（AMD）影响下水库沉积物中微量元素的质量分数水平及其分布特征,对常年受酸性废水影响的贵州兴仁猫石头水库沉积物中26种微量元素的质量分数、相关性及控制因素进行了分析。结果表明：猫石头水库沉积物柱中Sr、Ba、Zr、V、Cr和As质量分数平均值超过了100 μg/g,其中As质量分数最高,平均值超过800 μg/g;Be、Ta、Co、Ag、Cd、Sn和Se质量分数的平均值都在5 μg/g以下;其他元素质量分数平均值则在10~60 μg/g之间。相较未受AMD影响的水系沉积物,研究区水库沉积物具有明显的As和Sb富集特征。水库沉积物中Li、Be、Rb、Sr、Cs、Ba、Sc、Y、Zr、Hf、Nb、Ta、Th之间存在显著正相关关系,而As与这些元素之间存在显著负相关关系。元素相关分析、因子分析及微量元素图解表明,Li、Be、Rb、Sr、Cs、Ba、Sc、Y、Zr、Hf、Nb、Ta、Th、Cr、Sb等元素受控于流域岩石化学风化和土壤物理侵蚀,这也是控制研究区元素分布最重要的因素,而Cu、Cd等重金属元素则与AMD对地层中元素的溶蚀析出和有机质等细颗粒物的吸附有关。另外,研究区重金属元素中,Cd、Cu、Pb、Cr、Zn的生态风险轻微,而As和Sb则具有很强的潜在生态风险。     

NEW TRACE ELEMENT AND REE DATA IN THIRTEEN GSF REFERENCE SAMPLES BY ICP-MS

Analytical data on 34 geochemically significant trace elements (Sc, V, Cr, Co, Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Cs, Ba, Hf, Ta, Pb, The, U and REE) by using Inductively Coupled Plasma Mass Spectrometry (ICP-MS), for 13 reference rock samples obtained from the Geological Survey of Finland are presented. For many elements, especially most of the heavy-REE, concentrations are reported here for the first time.     

Concentration and distribution of elements in Late Permian coals from western Guizhou Province,China

With the aim of better understanding geochemistry of coal, 71 Late Permian whole-seam coal channel samples from western Guizhou Province, Southwest China were studied and 57 elements in them were determined. The contents of Al, Ca, Co, Cr, Cu, Fe, Ga, Hf, K, Li, Mn, Mo, Nb, Ni, Sn, Ta, Ti, Th, U, V, Zr, and REEs in the Late Permian coals from western Guizhou Province are higher than the arithmetic means for the corresponding elements in the US coals, whereas As, Ba, Br, F, Hg, P, Se, and Tl are lower. Compared to common Chinese coals, the contents of Co, Cr, Cu, Ga, Hf, Li, Mn, Mo, Ni, Sc, Sn, Ti, U, V, Zn, and Zr in western Guizhou coals are higher, and As, F, Hg, Rb, Sb, Tl, and W are lower. Five groups of elements may be classified according to their mode of occurrence in coal: The first two, Group A, Tm–Yb–Lu–Y–Er–Ho–Dy–Tb–Ce–La–Nd–Pr–Gd–Sm, and Group B, As–Sr–K–Rb–Ba–F–Ash–Si–Sn–Ga–Hf–Al–Ta–Zr–Be–Th–Na, have high positive correlation coefficients with ash yield and they show mainly inorganic affinity. Some elements from Group B, such as Ba, Be, Ga, Hf, and Th, are also characterized by significant aluminosilicate affinity. In addition, arsenic also exhibits high sulfide affinity (r_S–Fe>0.5). The elements, which have negative or lower positive correlation coefficients with ash yield (with exceptions of Bi, Cs, Nb, Mn, Se, and Ti), are grouped in other four associations: Group C, Cr–V–Mo–U–Cd–Tl; Group D, Hg–Li–Sc–Ti–Eu–Nb–Cs–W; Group E, Bi–Sb; and Group F, Co–Ni–Cu–Pb–Zn–Mg–Se–Ca–Mn–S–Fe. The correlation coefficients of some elements, including Co, Cr, Cu, Fe, Hg, Li, Mo, Ni, P, S, Sc, U, V, and Zn, with ash yield are below the statistically significant value. Only Cr and Cu are negatively correlated to ash yield (−0.07 and −0.01, respectively), showing intermediate (organic and inorganic) affinity. Manganese and Fe are characterized by carbonate affinity probably due to high content of epigenetic veined ankerite in some coals. Phosphorus has low correlation coefficients with any other elements and is not included in these six associations. There are five possible genetic types of enrichment of elements in coal from western Guizhou Province: source rock, volcanic ash, low-temperature hydrothermal fluid, groundwater, and magmatic hydrothermal inputs.     

Chemistry of Aerosols over Chukchi Sea and Bering Sea

The contents of elements in aerosols sampled during the First Chinese Arctic Research Expedition (CHINARE-1) show great differences from one element to another. Na, K,Ca, Mg, A1, F, and Cl are the major components in the aerosols, whose contents are larger than 30 ng/m^3. The chemical elements whose contents vary between 0.1 - 30 ng/m^3 are Br,Sr, Cr, Ni, and Zn. The chemical elements whose contents are close to or slightly higher than 0.1 ng/m^3 are Rb, Ba, Zr, Th, and Pb. The contents of As, Sb, W, Mo, Au, La, Ce, Nd,Sin, Eu, Tb, Yb, Lu, Sc, Co, Hf, Ta, and Cd are less than 0.1 ng/m^3. The mass concentration data for the same element, as observed during CHINARE-1, are almost accordant, but much lower than what is observed in the China‘ s seas or the coasts of China. The enrichment factor and electron microscopic analyses and lead isotope tracing were used to distinguish their sources.Four groups of sources can be classified as follows: anthropogenic: As, Sb, W, F, Mo, Au,Cu, Pb, Cd, V; crustal: La, Ce, Nd, Sm, Eu, Tb, Yb, Lu, Fe, Sc, Cr, Co, Ba, Zr, Hf,Ta, Cs, Mn, Th, U; oceanic:Na, K, Ca, and Mg; and mixing: Rb, Sr, Ca, and Mg.     

Instrumental Neutron Activation Analysis of Two French Geochemical Reference Samples - Basalt BR and Biotite Mica-Fe

Instrumental neutron activation analysis results for 20 trace elements (Sc, Cr, Co, Ni, Rb, Cs, Ba, La, Ce, Nd, Sm, Eu, Gd, Tb, Tm, Yb, Lu, Hf, Ta, Th) and for two major elements (Na and Fe) in two geochemical reference samples issued by the "Centre de Recherches Pétrographiques et Géochimiques" are reported and compared with available literature values. In general our results agree well with recommended or proposed values.     

Instrumental Thermal Neutron Activation Determination of 20 Elements in Nineteen Silicate Reference Materials

Elemental concentrations of Al, Ba, Ca, Ce, Co, Cr, Cs, Dy, Eu, Fe, Hf, Mn, Na, Rb, Sb, Sc, Ta, Th, Ti and V have been measured in 11 USGS, 6 CCRMP and 2 NBS reference materials by instrumental thermal neutron activation analysis. The results are compared with recent consensus and agency values.     

Instrumental Neutron Activation Analysis Of French Geochemical Reference Samples

Instrumental neutron activation analytical data, for eighteen trace elements (Ba, Co, Cr, Cs, Hf, Rb), Sb, Sc, Ta, Th, La, Ce, Nd, Sm, Eu, Tb, Yb, Lu), Hd₂O and Fe₂0₃ in eleven French geoche-mical reference samples are presented and discussed briefly.     

Trace Element Geochemistry of the Permian／Triassic Boundary Section in the Selong—Xishan Area,Nyalam County,Southern Tibet,China

Samples were collected f5rom the Selong-Xishan Permian/Triassic boundary strata,Nyalam County in southern Tibet and systematically analyzed for their rare-earth elements(REE) and trace elements such as U,Th,Sr,Ba,Sc,Ta,Hf,Rb,Cs,Co,Ni,Cr,As and others with emphasis put on the distribution patterns of rare-earth elements and the variation of trace element contents along the Permial/Triassic boundary section.On this basis a discussion will be made of the paleo-ocean depositional environment.     

A relative sea-level history for Arviat,Nunavut, and implications for Laurentide Ice Sheet thickness west of Hudson Bay

Thirty-six new and previously published radiocarbon dates constrain the relative sea-level history of Arviat on the west coast of Hudson Bay. As a result of glacial isostatic adjustment (GIA) following deglaciation, sea level fell rapidly from a high-stand of nearly 170 m elevation just after 8000 cal yr BP to 60 m elevation by the mid Holocene (~ 5200 cal yr BP). The rate of sea-level fall decreased in the mid and late Holocene, with sea level falling 30 m since 3000 cal yr BP. Several late Holocene sea-level measurements are interpreted to originate from the upper end of the tidal range and place tight constraints on sea level. A preliminary measurement of present-day vertical land motion obtained by repeat Global Positioning System (GPS) occupations indicates ongoing crustal uplift at Arviat of 9.3 ± 1.5 mm/yr, in close agreement with the crustal uplift rate inferred from the inferred sea-level curve. Predictions of numerical GIA models indicate that the new sea-level curve is best fit by a Laurentide Ice Sheet reconstruction with a last glacial maximum peak thickness of ~ 3.4 km. This is a 30–35% thickness reduction of the ICE-5G ice-sheet history west of Hudson Bay.     

西天山阿吾拉勒一带伊什基里克组火山岩地球化学特征及构造环境

西天山阿吾拉勒一带晚石炭世伊什基里克组为一套以钙碱性系列为主、碱性系列次之的双峰式火山岩建造,其中玄武岩类以碱性为主.岩石富FeO、Hf、Th、Y、Rb、Ba、Sc、Zr、Cs、V和LREE,贫TiO2、MgO、P2O5、Cr和Nb,岩石组合及地球化学各种参数和图解均证实,其形成于大陆板内裂谷环境.伊什基里克组火山岩是证实阿吾拉勒地区晚石炭世演化为大陆板内裂谷环境的重要记录.