Nd/Nd and Sm/Nd stratigraphy of Upper Ordovician epeiric sea carbonates

Stratigraphic changes in the ε_Nd of epeiric sea carbonates from central North America track the submergence history of the interior craton during the Late Ordovician. Fluctuations in sea level changed the Nd isotope balance of the epeiric sea by modifying the flux of Nd weathered from the highlands of the Taconic Orogen (ε_Nd = −6 to −9) and from the low relief Precambrian basement (ε_Nd = −22 to −15) of the Transcontinental Arch and Canadian Shield. Transgressions over the Arch and Shield, which diminished the weathering flux of Nd from the Precambrian basement, are recorded as positive shifts in the ε_Nd profiles of carbonates. Negative ε_Nd shifts reflect regression and reexposure of the Precambrian basement to erosion. Correlation of Upper Ordovician carbonates by use of the ε_Nd profiles demonstrates the potential for Nd isotope stratigraphy. Comparison of stratigraphic variations in carbonate Sm/Nd ratios with sea level curves, conodont paleoecology, and the ε_Nd profiles suggest that our observed variations in Sm/Nd ratios are related to changes in depth. Increasing Sm/Nd ratios correlate with increasing depth, whereas decreasing Sm/Nd ratios correlate with decreasing depth. This relationship between Sm/Nd ratios and depth suggests Sm/Nd profiles have potentially wide applications in understanding the paleoceanography of ancient epeiric seas.     

Behavior of Sm and Nd in a lateritic soil profile

A study of lateritic soils and samples of ground and river waters was carried out in the Nsimi-Zoetele, a tropical watershed in the southern Cameroon. The Nd isotopic compositions and concentrations of Nd and Sm were determined. It was found that the Nd isotopic composition of the river waters was much more radiogenic than the parent rocks, and that the Nd in the waters is not homogeneous but is carried by different dissolved and complexed components that are not isotopically homogenized. The soil profile shows a regular increase in ε_Nd going from the parent rock (ε_Nd = −36) to ε_Nd = −18 near the top of the profile. The Nd transported in the river is thus not representative of the parent rock but reflects the results of differential weathering of constituent minerals and the redeposition of REE in phosphates and a significant contribution of radiogenic Nd from dust. The concentration of Nd in the river water is far above that found in temperate climate rivers and thus this type of tropical river may play a dominant role in the marine Nd and REE budget. It is suggested that the correlation of REE with DOC is related to DOC fixing some dissolved REE but that the REE in solution is governed by other mechanisms. No major shifts were found in Sm/Nd; however, a regular progression from the parent rock through the lateritic profile was found. The upper laterite profile shows large, almost uniform depletions in all REE below Tb and enrichment above. Complementary behavior was found in the lower part of the section. The concentration of Nd relative to the immobile elements Zr and Ti in the laterite is depleted by a factor of ∼10. Th, Nd and Sm are enriched in the lowest zone sampled and must reflect redeposition of REE from the upper part of the weathering section and is associated with phosphate formation. It is concluded that the soil evolution involves both differential dissolution of primary phases from the parent rock, significant to major input of REE from atmospheric dust from other regions, and the formation of diagenetic phases, particularly phosphates.     

Nd and Sr isotope compositions in modern and fossil bones - Proxies for vertebrate provenance and taphonomy

Rare earth elements (REE), while not essential for the physiologic functions of animals, are ingested and incorporated in ppb concentrations in bones and teeth. Nd isotope compositions of modern bones of animals from isotopically distinct habitats demonstrate that the ¹⁴³Nd/¹⁴⁴Nd of the apatite can be used as a fingerprint for bedrock geology or ambient water mass. This potentially allows the provenance and migration of extant vertebrates to be traced, similar to the use of Sr isotopes. Although REE may be enriched by up to 5 orders of magnitude during diagenesis and recrystallization of bone apatite, in vivo¹⁴³Nd/¹⁴⁴Nd may be preserved in the inner cortex of fossil bones or enamel. However, tracking the provenance of ancient or extinct vertebrates is possible only for well-preserved archeological and paleontological skeletal remains with in vivo-like Nd contents at the ppb-level. Intra-bone and -tooth REE analysis can be used to screen for appropriate areas. Large intra-bone Nd concentration gradients of 10¹-10³ are often measured. Nd concentrations in the inner bone cortex increase over timescales of millions of years, while bone rims may be enriched over millenial timescales. Nevertheless, ε_Nd values are often similar within one ε_Nd unit within a single bone. Larger intra-bone differences in specimens may either reflect a partial preservation of in vivo values or changing ε_Nd values of the diagenetic fluid during fossilization. However, most fossil specimens and the outer rims of bones will record taphonomic ¹⁴³Nd/¹⁴⁴Nd incorporated post mortem during diagenesis. Unlike REE patterns, ¹⁴³Nd/¹⁴⁴Nd are not biased by fractionation processes during REE-uptake into the apatite crystal lattice, hence the ε_Nd value is an important tracer for taphonomy and reworking. Bones and teeth from autochthonous fossil assemblages have small variations of ±1 ε_Nd unit only. In contrast, fossil bones and teeth from over 20 different marine and terrestrial fossil sites have a total range of ε_Nd values from -13.0 to 4.9 (n = 80), often matching the composition of the embedding sediment. This implies that the surrounding sediment is the source of Nd in the fossil bones and that the specimens of this study seem not to have been reworked. Differences in ε_Nd values between skeletal remains and embedding sediment may either indicate reworking of fossils and/or a REE-uptake from a diagenetic fluid with non-sediment derived ε_Nd values. The latter often applies to fossil shark teeth, which may preserve paleo-seawater values. Complementary to ε_Nd values, ⁸⁷Sr/⁸⁶Sr can help to further constrain the fossil provenance and reworking.     

Coupling of anatectic reactions and dissolution of accessory phases and the Sr and Nd isotope systematics of anatectic melts from a metasedimentary source

Advances in field observations and experimental petrology on anatectic products have motivated us to investigate the geochemical consequences of accessory mineral dissolution and nonmodal partial melting processes. Incorporation of apatite and monazite dissolution into a muscovite dehydration melting model allows us to examine the coupling of the Rb-Sr and Sm-Nd isotope systems in anatectic melts from a muscovite-bearing metasedimentary source. Modeling results show that (1) the Sm/Nd ratios and Nd isotopic compositions of the melts depend on the amount of apatite and monazite dissolved into the melt, and (2) the relative proportion of micas (muscovite and biotite) and feldspars (plagioclase and K-feldspar) that enter the melt is a key parameter determining the Rb/Sr and ⁸⁷Sr/⁸⁶Sr ratios of the melt. Furthermore, these two factors are not, in practice, independent. In general, nonmodal partial melting of a pelitic source results in melts following one of two paths in ε_Nd-⁸⁷Sr/⁸⁶Sr ratio space. A higher temperature, fluid-absent path (Path 1) represents those partial melting reactions in which muscovite/biotite dehydration and apatite but not monazite dissolution play a significant role; the melt will have elevated Rb/Sr, ⁸⁷Sr/⁸⁶Sr, Sm/Nd, and ε_Nd values. In contrast, a lower temperature, fluid-fluxed path (Path 2) represents those partial melting reactions in which muscovite/biotite dehydration plays an insignificant role and apatite but not monazite stays in the residue; the melt will have lower Rb/Sr, ⁸⁷Sr/⁸⁶Sr, Sm/Nd, and ε_Nd values than its source. The master variables controlling both accessory phase dissolution (and hence the Sm-Nd system), and melting reaction (and hence the Rb-Sr systematics) are temperature and water content. The complexity in Sr-Nd isotope systematics in metasediment-derived melts, as suggested in this study, will help us to better understand the petrogenesis for those granitic plutons that have a significant crustal source component.     

Neodymium isotopes in the Mediterranean Sea: comparison between seawater and sediment signals

Nine depth-profiles of dissolved Nd concentrations and isotopic ratios (ε_Nd) were obtained in the Levantine Basin, the Ionian, the Aegean, the Alboran Seas and the Strait of Gibraltar. Thirteen core-top sediments and Nile River particle samples were also analyzed (leached with 1 N HCl, acetic acid or hydroxylamine hydrochloride). The seawater ε_Nd values become more radiogenic during the eastward circulation in the Mediterranean Sea. The relationship between salinity and the seawater ε_Nd shows that the Nd isotopic signature is more conservative than salinity in the Mediterranean Sea. The water mass with the highest ε_Nd (−4.8) is found at about 200 m in the easternmost Levantine basin. The average ε_Nd value for deep waters is −7.0 in the eastern basin, 2.5 ε-units higher than in the western basin. By examining the sensitivity of seawater ε_Nd to Nd inputs from the Nile, we conclude that the most significant radiogenic Nd source is partially dissolved Nile River particles. The Nd flux from the Nile River water has a minor influence on the Mediterranean seawater ε_Nd. Except for the easternmost Levantine Basin, the leachate ε_Nd values are consistent with the seawater values. In the easternmost Levantine Basin, the leachate ε_Nd values obtained with HCl leaching are systematically higher than the seawater values. The relationship between leachate and residual ε_Nd values indicates that the HCl leaching partially dissolves lithogenic Nd, so the dissolution of Nile River particles is the cause of the observed shift. Some ε_Nd values obtained with hydroxylamine hydrochloride leaching are higher than those obtained with HCl leaching. Although the reason for this shift is not clear, ⁸⁷Sr/⁸⁶Sr successfully detects the presence of a nonmarine component in the leachate. Our results suggest that leaching performance may vary with the mineralogy of marine sediments, at least in the case of the Mediterranean Sea.     

Geochemical Characteristics of Eolian Deposits in the Chengdu Plain of Sichuan Province and the Implications for Provenance

In this study Chengdu Red Earth （CRE） from the Chengdu Plain （CP）,Sichuan province,was analyzed for its elemental （major and trace elements） and isotopic （Sm-Nd） geochemistry and compared with Pleistocene loess and paleosol samples from the Chinese Loess Plateau （CLP） in Northern China.The geochemical composition of CRE is similar to north China loess,and also resembles the average UCC.This indicates that CRE,as loess deposits in Northern China,was derived from well-mixed sedimentary protoliths that have undergone numerous upper crustal recycling processes.However,obvious differences in the geochemical characteristics of CRE and the north China loess are also revealed in our results.For chemically stable elements,CRE has higher Ti,Zr,Hf and lower ΣREE,Ba contents in comparison with loess samples from the CLP.Further analysis shows that CRE has higher TiO2/Al2O3,SiO2/Al2O3,Ba/Rb and lower Ce/Yb,Eu/Yb,LaN/YbN and ΣLREE/ ΣHREE ratios.In Sm-Nd isotopic geochemistry,Sm and Nd content and the εNd（0） value in CRE are significantly higher than those in north China loess.The higher TiO2 content in CRE coincided with a high background concentration of Ti in the Sichuan Basin and the surrounding regions.The lower ΣREE and higher Sm,Nd,εNd（0） values are related to the wide distribution of basalt in the southwest Sichuan Basin.The elemental and isotopic geochemistry of CRE indicates that eolian materials in the CP predominantly come from the Sichuan Basin and the surrounding regions,which differs from loess deposits in the CLP.     

Nd isotopic composition of Late Devonian seawater in western Thailand: Geotectonic implications for the origin of the Sibumasu terrane

Conodonts collected from sections near the small towns of Thong Pha Phum and Mae Sariang in the westernmost part of Thailand are used to reconstruct the neodymium (Nd) isotopic composition of seawater during the Late Devonian. The study provides the first Devonian seawater signatures recognized within the Australian shelf of northeastern Gondwana and the adjacent Paleotethys Ocean. At Thong Pha Phum site, the seawater was characterized by very low ε_Nd values (from − 13.1 to − 18.2) and very high Sm/Nd ratios (between 0.36 and 0.66). In contrast, the seawater at the Mae Sariang site was characterized by much more radiogenic signatures (ε_Nd values from − 8.7 to − 11.1) and uniform, low Sm/Nd ratios (between 0.20 and 0.23). Extremely low ε_Nd values recognized at Thong Pha Phum attest to a passive margin continental setting and a paleogeographic position very close to a continental area where Paleoproterozoic and Neoarchean rocks were eroded. Thus, the isotopic data provide strong evidence that during Late Devonian time the Sibumasu terrane was situated in the proximity to the Archean cratons of Western Australia, presumably adjacent to the Carnarvon intracratonic basin. Moreover, Sibumasu may not have been situated in an outboard position on the shelf, as previously suggested, but could have been directly attached to the Australian continental crust. By contrast, low and uniform Sm/Nd ratios of seawater at Mae Sariang resemble those of the Variscan and the present-day oceanic seawaters. Therefore, a pelagic setting within the Paleotethys Ocean is postulated for the Mae Sariang succession. This conclusion is also constrained by minor temporal changes in ε_Nd values and suggests that the Paleozoic of Mae Sariang is not part of the Sibumasu terrane but belongs to the Inthanon Zone.     

The Behaviour of Rare—Earth Elements（REE） During Weathering of Granites in Southern Guangxi,China

The behaviour of the rare-earth elements(REE)during the weathering of granites was studied in southern Guangxi,China.Based on the study of the weathering profiles,the soil,weathered and sub-weatereb zones are identified with different REE geochemical behaviours throug the weathering profiles of granite.The Ce anomalies of the weathering profiles cover a large range of values with most falling between 1.02 and 1.43in the soil zone and 0.16and 0.40in the weathered and sub-weathered zones.Light rare-earth elements(LREE) and heavy rare-earth elements(HREE)are enriched to varying degree in the weathering profiles as compared to host granites.In the soil zone,more HREEs are leached than LREEs,and HREEs are more enriched than LREE in the weathered and sub-weathered zones.It is considered that infiltration and adsorption on clays are two processes controlling the enrichment and formation of REE deposits in the weathering profiles of granite.     

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.     

苏皖玄武岩土壤中风尘的识别及风化特征

风尘传输与沉降影响生态系统和元素的生物地球化学循环,对其在成壤作用中的识别与贡献进行研究有重要意义。文章选择在非风尘沉降区的苏皖玄武岩台地典型的两个风化剖面（安徽明光梅花村和江苏盱眙宝塔村）和部分表土及水系沉积物样品,系统分析主要矿物、粘土矿物、常量元素、微量元素及Sr、Nd同位素组成。结果显示,玄武岩基岩基本由斜长石和辉石组成,而风化基岩则主要由蒙脱石构成,风化土壤则出现基岩和风化基岩中未出现的石英、伊利石等风尘特征矿物;基岩和风化基岩以高Mg,低Si、K,无Eu异常等特征,风化土壤则以高Si、K,低Mg,负Eu异常等特征;基岩和风化基岩的εNd偏正,⁸⁶Sr/⁸⁷Sr值较低,而风化土壤εNd偏负,⁸⁶Sr/⁸⁷Sr值较高;各种证据都显示风尘对风化土壤有重要贡献,通过Nd同位素混合模式计算,风尘对土壤的贡献达60%以上。玄武岩风化表现为完全的蒙脱石化,为显著的去Ca、Mg作用,在梅花村剖面,表层土壤出现Ce负异常,而在下部层位出现Ce正异常,研究还发现在风尘的加积作用,土壤的Si、K含量得以上升。受相对较大的玄武岩台地高程差影响,玄武岩风化产物和沉降的风尘易被降水侵蚀,造成风化剖面较薄,促使玄武岩风化处于“供应限制”模式。本次工作为玄武岩的风化机制,风尘在元素地球化学循环中的作用等提供了新的地质证据。     

Isotopic-geochemical evidence for crustal contamination of eclogites in the Kokchetav subduction-collision zone

This paper reports isotopic and geochemical studies of eclogites from the western ultrahigh pressure (UHP) and eastern high-pressure (HP) blocks of the Kokchetav subduction-collision zone. These HP and UHP eclogites exhumed in two stages: (1) The rocks of the western block metamorphosed within the field of diamond stability (e.g., Kumdy-Kol and Barchy); (2) In contrast, the metamorphic evolution of the eastern block reached the pressure peak within the stability field of coesite (e.g., Kulet, Chaglinka, Sulu-Tyube, Daulet, and Borovoe). The eclogites vary widely in the ratios of incompatible elements and in the isotope ratios of Nd (¹⁴³Nd/¹⁴⁴Nd = 0.51137-0.513180) and Sr (⁸⁷Sr/⁸⁶Sr = 0.703930.78447). The Sulu-Tyube eclogites display isotope-geochemical features close to N-MORB, while those from the other sites are compositionally similar to E-type MORB or island arc basalts (IAB). The model ages T_Nd(DM) of eclogites vary between 1.95 and 0.67 Ga. The Sulu-Tyube eclogite yields the youngest age; it has the values of ε_Nd(T) (7.2) and ⁸⁷Sr/⁸⁶Sr (0.70393) close to the depleted mantle values. The crustal input to the protolith of the Kokchetav eclogites is evident on the ε_Nd(T)-⁸⁶Sr/⁸⁷Sr and ε_Nd(T)-T plots. The eclogites make up a trend from DM to country rocks. Some eclogites from the Kulet, Kumdy-Kol, and Barchy localities display signs of partial melting, such as high Sm/Nd (0.65-0.51) and low (La/Sm)_N (0.34-0.58) values. The equilibrium temperatures of these eclogites are higher than 850 °C. The geochemical features of eclogites testify to the possibility of the eclogite protolith formation in the tectonic setting of passive continental rift margin subducted to depths over 120 km.     

Mineralogical sources of the buffer capacity in a granite catchment determined by strontium isotopes

The role of different minerals in base cation release and thus the increase of buffering capacity of groundwater against acid deposition is controversially discussed in the literature. The ⁸⁷Sr/⁸⁶Sr ratios and base cation concentration were investigated in whole rock leachates, mineral separates, precipitation, soil solution, groundwater and stream water samples in the Lehstenbach catchment (Germany) to identify the weathering sequence of the granite bedrock. Three different approaches were followed in parallel. It was assumed that the contribution of different minerals to base cation supply of the groundwater with increasing weathering intensity would be observed by investigating (1) unweathered rock leachates, deep groundwater and shallow groundwater, (2) groundwater samples from new groundwater wells, reflecting the initial weathering of the drilled bedrock, and groundwater from wells that were drilled in 1988, (3) stream water during baseflow, dominated by deep groundwater, and stream water during high flow, being predominantly shallow groundwater. Whereas the first approach yielded consistent patterns, there was some evidence that groundwater from the new wells initially reflected contamination by the filter gravel rather than cation release in an initial stage of weathering. Time series samples of stream water and groundwater solute concentrations and isotope ratios turned out to reflect varying fractions of soil water and precipitation water at baseflow and high flow conditions rather than varying contributions of different minerals that prevail at different stages of granite weathering.     

Characterization and migration of atmospheric REE in soils and surface waters

Rainwater and snow collected from three different sites in France (Vosges Mountains, French Alps and Strasbourg) show more or less similar shapes of their REE distribution patterns. Rainwater from Strasbourg is the most REE enriched sample, whereas precipitations from the two mountainous, less polluted catchments are less REE enriched and have concentrations close to seawater. They are all strongly LREE depleted.Different water samples from an Alpine watershed comprising snow, interstitial, puddle and streamwater show similar REE distributions with LREE enrichment (rainwater normalized) but MREE and HREE depletion. In this environment, where water transfer from the soil to the river is very quick due to the low thickness of the soils, it appears that REE in streamwater mainly originate from atmospheric inputs. Different is the behaviour of the REE in the spring- and streamwaters from the Vosges Mountains. These waters of long residence time in the deep soil horizons react with soil and bedrock REE carrying minerals and show especially significant negative Eu anomalies compared to atmospheric inputs. Their Sr and Nd isotopic data suggest that most of the Sr and Nd originate from apatite leaching or dissolution. Soil solutions and soil leachates from the upper soil horizons due to alteration processes strongly depleted in REE carrying minerals, have REE distribution patterns close to those of lichens and throughfall. Throughfall is slightly more enriched especially in light REE than filtered rainwater probably due to leaching of atmospheric particles deposited on the foliage and also to leaf excretion.Data suggest that Sr and Nd isotopes of the soil solutions in the upper soil horizons originate from two different sources: 1) An atmospheric source with fertilizer, dust and seawater components and 2) A source mainly determined by mineral dissolution in the soil. These two different sources are also recognizable in the Sr and Nd isotopic composition of the tree’s throughfall solution. The atmospheric contributions of Sr and Nd to throughfall and soil solution are of 20 to 70 and 20%, respectively. In springwater, however, the atmospheric Sr and REE contribution is not detectable.     

Fluorite as an Sm–Nd geochronometer of hydrothermal processes: Dating of mineralization hosted in the Strel’tsovka uranium ore field,eastern Baikal region

The possibility of using hydrothermal fluorite as an Sm–Nd geochronometer is based on the results of an REE pattern study of this mineral (Chernyshev et al., 1986). As a result of REE fractionation, in many cases, the Sm/Nd ratio achieves a multifold increase compared with its level in terrestrial rocks, and the radiogenic shift of the ¹⁴³Nd/¹⁴⁴Nd isotope ratio reaches 10–20 ε_Nd units over a short time interval (as soon as tens of Ma). This is a necessary prerequisite for Sm–Nd isochron dating of fluorite. Zonal polychrome fluorite from a vein referred to the final stage of large-scale uranium mineralization at the Sterl’tsovka deposit in the ore field of the same name located in the eastern Transbaikal region has been dated using the ¹⁴³Nd/¹⁴⁴Nd method. To optimize isochron construction, local probes with high and contrasting Sm/Nd ratios have been sampled from the polished surfaces of two samples, taking into account the REE pattern of zonal fluorite. Sm–Nd isochron dating has been carried out separately for each sample. The ¹⁴⁷Sm/¹⁴⁴Nd и ¹⁴³Nd/¹⁴⁴Nd ratios vary within the intervals 0.5359–2.037 and 0.512799–0.514105, respectively. Two isochrons, each based on six fluorite probes, have been obtained with the following parameters, which coincide within 2σ uncertainty limits: (1) t = 134.8 ± 1.3 Ma, (¹⁴³Nd/¹⁴⁴Nd)₀ = 0.512310 ± 13, MWSD = 0.43 and (2) t = 135.8 ± 1.6 Ma, (¹⁴³Nd/¹⁴⁴Nd)₀ = 0.512318 ± 10, MWSD = 1.5. The mean age of fluorite based on two isochron datings is 135.3 ± 1 Ma. Comparison of this value with the most precise dating of pitchblende related to the ore stage in the Strel’tsovka ore field (135.5 ± 1 Ma) shows that four mineralization stages, distinguished by geological and mineralogical data, that were completed with the formation of polychrome fluorite veins 135.3 ± 1 Ma ago, represent a single and indivisible hydrothermal process whose duration does not exceed 1 Ma.     

Low-Sulfide PGE ores in paleoproterozoic Monchegorsk pluton and massifs of its southern framing,Kola Peninsula,Russia: Geological characteristic and isotopic geochronological evidence of polychronous ore–magmatic systems

New U–Pb and Sm–Nd isotopic geochronological data are reported for rocks of the Monchegorsk pluton and massifs of its southern framing, which contain low-sulfide PGE ores. U–Pb zircon ages have been determined for orthopyroxenite (2506 ± 3 Ma) and mineralized norite (2503 ± 8 Ma) from critical units of Monchepluton at the Nyud-II deposit, metaplagioclasite (2496 ± 4 Ma) from PGE-bearing reef at the Vurechuaivench deposit, and host metagabbronorite (2504.3 ± 2.2. Ma); the latter is the youngest in Monchepluton. In the southern framing of Monchepluton, the following new datings are now available: U–Pb zircon ages of mineralized metanorite from the lower marginal zone (2504 ± 1 Ma) and metagabbro from the upper zone (2478 ± 20 Ma) of the South Sopcha PGE deposit, as well as metanorite from the Lake Moroshkovoe massif (2463.1 ± 2.7 Ma). The Sm–Nd isochron (rock-forming minerals, sulfides, whole-rock samples) age of orthopyroxenite from the Nyud-II deposit (2497 ± 36 Ma) is close to results obtained using the U–Pb method. The age of harzburgite from PGE-bearing 330 horizon reef of the Sopcha massif related to Monchepluton is 2451 ± 64 Ma at initial ε_Nd =–6.0. The latter value agrees with geological data indicating that this reef was formed due to the injection of an additional portion of high-temperature ultramafic magma, which experienced significant crustal contamination. The results of Sm–Nd isotopic geochronological study of ore-bearing metaplagioclasite from PGE reef of the Vurechuaivench deposit (2410 ± 58 Ma at ε_Nd =–2.4) provide evidence for the appreciable effect of metamorphic and hydrothermal metasomatic alterations on PGE ore formation. The Sm–Nd age of mineralized norite from the Nyud-II deposit is 1940 ± 32 Ma at initial ε_Nd =–7.8. This estimate reflects the influence of the Svecofennian metamorphism on the Monchepluton ore–magmatic system, which resulted in the rearrangement of the Sm–Nd system and its incomplete closure. Thus, the new isotopic geochronological data record the polychronous development of the Monchegorsk ore–magmatic systems and the massifs in its southern framing.     

Geochemical and mineralogical characteristics of ion-adsorption type REE mineralization in Phuket, Thailand

Geochemical and mineralogical studies were conducted on the 12-m-thick weathering profile of the Kata Beach granite in Phuket, Thailand, in order to reveal the transport and adsorption of rare earth elements (REE) related to the ion-adsorption type mineralization. The parent rock is ilmenite-series biotite granite with transitional characteristics from I type to S type, abundant in REE (592 ppm). REE are contained dominantly in fluorocarbonate as well as in allanite, titanite, apatite, and zircon. The chondrite-normalized REE pattern of the parent granite indicates enrichment of LREE relative to HREE and no significant Ce anomaly. The upper part of the weathering profile from the surface to 4.5 m depth is mostly characterized by positive Ce anomaly, showing lower REE contents ranging from 174 to 548 ppm and lower percentages of adsorbed REE from 34% to 68% compared with the parent granite. In contrast, the lower part of the profile from 4.5 to 12 m depth is characterized by negative Ce anomaly, showing higher REE contents ranging from 578 to 1,084 ppm and higher percentages from 53% to 85%. The negative Ce anomaly and enrichment of REE in the lower part of the profile suggest that acidic soil water in an oxidizing condition in the upper part mostly immobilized Ce⁴⁺ as CeO₂ and transported REE³⁺ downward to the lower part of the profile. The transported REE³⁺ were adsorbed onto weathering products or distributed to secondary minerals such as rhabdophane. The immobilization of REE results from the increase of pH due to the contact with higher pH groundwater. Since the majority of REE in the weathered granite are present in the ion-adsorption fraction with negative Ce anomaly, the percentages of adsorbed REE are positively correlated with the whole-rock negative Ce anomaly. The result of this study suggests that the ion-adsorption type REE mineralization is identified by the occurrence of easily soluble REE fluorocarbonate and whole-rock negative Ce anomaly of weathered granite. Although fractionation of REE in weathered granite is controlled by the occurrence of REE-bearing minerals and adsorption by weathering products, the ion-adsorption fraction tends to be enriched in LREE relative to weathered granite.     

Weathering process at the natural fission reactor of Bangombé

 The uranium deposits in the basin of Franceville (Gabon) host the only natural fission reactors known in the world. Unique geological conditions favoured a natural fission reaction 2 Ga ago. This was detected by anomalous isotopic compositions of uranium and rare earth elements (REE), which are produced by the fission reaction. In total, 16 reactor zones were found. Most of them are mined out. The reactor zone of Bangombé, is only 10–11 m below the surface. This site has been influenced by surface weathering processes. Six drill cores have been sampled at the site of the reactor zone of Bangombé during the course of the study and only one drill core (BAX 08) hit the core of the reactor. From these data and previous drilling campaigns, the reactor size is estimated to be 10 cm thick, 2–3 m wide and 4–6 m long. The migration of fission products can be traced by the anomalous isotope ratios of REE because of the fission process. The ¹⁴⁹Sm/¹⁴⁷Sm ratio close to the reactor zone is only 0.28 (normal: 0.92) because of the intense neutron capture of ¹⁴⁹Sm and subsequent transmutation, whereas ¹⁴⁷Sm is enriched by the fission reaction. Similar changes in isotopic patterns are detectable on other REE. The isotope ratios of Sm and Nd of whole rock and fracture samples surrounding the reactor indicate that fission-genic REE migrated only a few decimetres above and mainly below the reactor zone. Organic matter (bitumen) seems to act as a trap for fission-genic REE. Additional REE-patterns show less intense weathering with increasing depth in the log profile and support a simple weathering model. Received: 26 November 1999 · Accepted: 2 May 2000     

Archean Enriched Mantle Beneath the Baltic Shield: Rare-Earth-Element Evidence from the Burakovsky Layered Intrusion,Southern Karelia,Russia

In order to better understand the origin and character of late-Archean mantle beneath the Baltic Shield, we have analyzed mafic-ultramafic rocks from one of the best-preserved, least-metamorphosed regions of Karelia, Russia. Trace-element data for samples from the ultramafic and gabbronorite zones of the large (700 km²) Burakovsky layered intrusion (BLI) are presented. Samples from the ultramafic zone are LREE enriched, indicating that they formed from a LREE-enriched parental magma. Indeed, a calculated parental magma for the ultramafic zone has a (Ce/Yb)_n ratio of 2.6, a (Nd/Sm)_n ratio of 1.1, and a (Dy/Yb)_n ratio of 1.6. The LREE enrichment in the parental magma suggests either that the source region was LREE enriched or that the melt was contaminated by crust en route to the BLI magma chamber. Samples from the gabbronorite zone also are LREE enriched and indicate two distinct parental magmas. Group-I magmas, from the lower part of the gabbronorite zone, have (Ce/Yb)_n ratios of 6.9 to 13.9, whereas Group-II magmas, from the upper portion, have (Ce/Yb)_n ratios of 15.8 to 27.3. Volcanic rocks in Karelia that are coeval to the Burakovsky layered intrusion, as well as volcanic rocks of a similar age in other parts of the Baltic Shield, also are LREE enriched. Furthermore, the BLI has an initial ε_Nd value of ?2.0, and other layered intrusions in the Baltic Shield of similar age also have negative initial ε_Nd values (e.g., ?1.8 to ?2.2). The consistency of these ε_Nd values for layered intrusions throughout Karelia precludes contamination as a controlling factor in their isotopic compositions. All of these data are most consistent with the development of LREE-enriched mantle beneath the eastern Baltic Shield, prior to the earliest Proterozoic.     

Source characteristics of the ∼2.5 Ga Wangjiazhuang Banded Iron Formation from the Wutai greenstone belt in the North China Craton: Evidence from neodymium isotopes

Here we first present samarium (Sm)–neodymium (Nd) isotopic data for the ∼2.5 Ga Wangjiazhuang BIF and associated lithologies from the Wutai greenstone belt (WGB) in the North China Craton. Previous geochemical data of the BIF indicate that there are three decoupled end members controlling REE compositions: high-T hydrothermal fluids, ambient seawater and terrigenous contaminants. Clastic meta-sediment samples were collected for major and trace elements studies in an attempt to well constrain the nature of detrital components of the BIF. Fractionated light rare earth elements patterns and mild negative Eu anomalies in the majority of these meta-sedimentary samples point toward felsic source rocks. Moreover, the relatively low Th/Sc ratios and positive ε_Nd(t) values are similar to those of the ∼2.5 Ga granitoids, TTG gneisses and felsic volcanics in the WGB, further indicating that they are derived from less differentiated terranes. Low Chemical Index of Weathering (CIW) values and features in the A-CN-K diagrams for these meta-sediments imply a low degree of source weathering. Sm–Nd isotopes of the chemically pure BIF samples are characterized by negative ε_Nd(t) values, whereas Al-rich BIF samples possess consistently positive ε_Nd(t) features. Significantly, the associated supracrustal rocks in the study area have positive ε_Nd(t) values. Taken together, these isotopic data also point to three REE sources controlling the back-arc basin depositional environment of the BIF, the first being seafloor-vented hydrothermal fluids (ε_Nd(t) < −2.5) derived from interaction with the underlying old continental crust, the second being ambient seawater which reached its composition by erosion of parts of the depleted landmass (likely the arc) (ε_Nd(t) > 0), the third being syndepositional detritus that received their features by weathering of a nearby depleted source (likely the arc) (ε_Nd(t) > 0).     

The Composition and Age of the Mesoarchean Gabbro in the South Vygozersky and Kamennoozersky Greenstone Structures,Karelia

The geochemical and zircon geochronological (U-Pb, SHRIMP-II) study of Mesoarchean gabbros of the South Vygozersky and Kamennoozersky greenstone structures of Central Karelia made it possible to distinguish four gabbro types: (1) Fe–Ti gabbro, 2869 ± 12 Ma, (2) gabbro compositionally close to tholeiitic basalts, 2857 ± 7 Ma, (3) leucogbabbro, 2840 ± 5 Ma; and (4) melanogabbro, 2818 ± 14 Ma. From the early to late gabbros, the rocks are depleted in Ti, Fe, V, Y, Zr, Nb, Hf, REE and enriched in Mg, Ca, Cr, Ni. According to the systematics (Condie, 2005), the Nb/Y, Zr/Y, Zr/Nb ratios in the studied Late Archean gabbros are close to those of primitive mantle, while the gabbros in composition are similar to those of plumederived ocean-plateau basalts. Their magma sources were derived from different mantle reservoirs. The leucogabbro and melanogabbro with similar εNd = +4 were derived from a depleted mantle source (DM). The gabbro close in composition to tholeiitic basalts and having the elevated positive ε_Nd (+4.9) was derived from a strongly depleted mantle source. Insignificant admixture of crustal material or lithospheric mantle is inferred in a source of the Fe–Ti gabbro (with lowest ε_Nd = +2.1).