In the Bengal Delta Plain (BDP) the primary arsenic sourcing appears to be different from the global scenario. Here, the Terminal Pleistocene–Holocene depositional platform, the interactive early Holocene depositional morphology with fluvio-estuarine and marine incursions played a crucial role for arsenic sourcing and enrichment. The lenticular silt-fine sand layer between anoxic clay beds favoured entrapment of dissolved organic carbon with decayed phyto-planktons debris. The Terminal Pleistocene–Holocene transgression and regression processes may have acted as major events in the BDP. Interestingly, at the end of the last glacial maxima, the Pleistocene delta had undergone block movements, wherein some parts of the platform were raised above the level of Holocene deposition. Those blocks were found to be free from arsenic in the groundwater. The sea, during re-emerging inundation (10–7 ka BP), has witnessed a monsoon-induced environment in the BDP with the resultant oscillation of sea level leading to higher upsurge towards the north. This might have resulted in the marine incursion and inundation in pre-existing land depressions. Meanwhile arsenic entrapments through marine incursion as well as enrichment in the presence of organic carbon/DOC and/or Fe/Mn/Al catalytic agents could have developed into localised redox traps. It may be of relevance that due to the repetitive transgressive–regressive phases in Holocene, resulting in periodic exposure and weathering of iron-bearing minerals and consequent iron enrichment in the aquifer system. The iron, thus present, had free charge to host arsenic as a sink. It appears that arsenic, wherever found, would likely be of atypical localised exhaustible phenomenon, both in horizontal and vertical context. It also rationalises the cause of the absence of arsenic in the other nearby Pleistocene platform, which has not come across Holocene interaction and marine incursion, as to the likely limiting condition for the search for arsenic in the BDP or beyond. 相似文献
TTG(Tonalite-Trondhjemite-Granodiorite) gneisses,a major component of Precambrian continental crust,play a significant role in understanding the process and mechanism of the crustal evolution in the early periods of the Earth. In terms of field occurrence,there are two kinds of Archean TTGs in the NCC(North China Craton): intercalated and non-intercalated TTGs. In this contribution,we make a comprehensive comparison of these two types of TTGs from the typical areas(Lushan and Hengshan) in the NCC with an aim to constrain their petrogenesis. The results suggest that they have similar mineral assemblages of Pl + Qtz + Bt ± Amp ± Kfs but different field appearances and geochemical compositions,thus probably reflecting different source materials and tectonic settings. Differences in the contents of characteristic elements,such as Sr,REE and HFSE,suggest that the nonintercalated TTGs in Hengshan were generated at deeper levels than those of intercalated TTGs in Lushan. Constraints from element contents and geochemical modeling results are consistent with derivation from dual sources involving both garnet amphibolite and rutile-bearing eclogite residues for the non-intercalated TTGs in Hengshan,whereas the compositions of intercalated TTGs in Lushan indicate that they were formed by partial melting with amphibolite to garnet-amphibolite residues. Moreover,accumulation of plagioclase is also required in the petrogenesis of intercalated TTGs in Lushan,at least for part of them. In addition,the non-intercalated TTGs in Hengshan display distinctly higher Mg O,Mg#,Cr and Ni values and lower SiO_2 average contents compared to the intercalated TTGs in Lushan. These features suggest that the former magma,at least a part,might have interacted with the mantle wedge during ascent. Considering all the above factors and in combination with the whole-rock Nd and zircon Hf isotopic data,it is suggested that the non-intercalated TTGs in Hengshan were produced by partial melting of subducted slab contaminated by the overlying mantle wedge at deeper levels and high pressures,whereas the intercalated TTGs in Lushan were generated by melting of the thickened lower crust at lower pressures and shallower depths. The tectonic settings of the two types of TTGs shed new light on the growth of the NCC. 相似文献
Trace-element geochemistry of sandstones are being used to determine provenance. We have conducted preliminary and limited experiments to determine to what extent daughter sands retain the geochemical signature of parent rocks. Six sets of first-order stream sediments, soils from adjacent slopes, and a variety of parent rocks were collected from southwestern Montana, U.S.A. Sampling in a low-relief area ensured that climate and residence time of soils on slopes could be eliminated as variables. Sand-size fractions of stream sediments and soils, and the corresponding parent rocks (granodiorite, quartz monzonite, granite gneiss, biotite-tonalite gneiss and amphibolite) were analyzed for most major elements and selected trace elements. Petrologic modal analysis of the parent rocks and the 0.25–0.50-mm fraction of each sand was done to monitor major mineralogic control, if any, on chemical compositions of the samples.
Our data show that the abundances of the Si and Al in sediments do not discriminate provenance. Abundances of Ca, Mg, Fe and Ti may broadly distinguish between sands derived from metamorphic and igneous source rocks, at least in the area studied. Differences in abundances of the Ba and Th, and the ratio of La/Lu between granitic, tonalitic and amphibolitic parent rocks are preserved in the daughter sediments that we studied. However, the size of the Eu anomaly in the REE patterns of different daughter sediments is not diagnostic of parent rocks. Abundances of Co and Sc distinguish between sediments derived from felsic and mafic rocks. A better provenance discrimination is obtained if the ratios La/Sc, Th/Sc, La/Co, Ba/Sc and Ba/Co are used.
Petrologic modal data show that mineral contents and chemical compositions of parent rocks are compatible with each other. The chemical composition of the sands may be roughly correlated to the petrological modal data but the abundances of some minor and trace elements of sediments cannot be inferred from modal mineralogy. This is expected because these elements may concentrate in accessory minerals and/or may weather out into aqueous or clay mineral fractions; it is also compatible with conclusions of previous studies that some of these elements do not reside in sand-size fractions of siliciclastic sediments. 相似文献
Wudalianchi volcanic rocks are the most typical Cenozoic potassic volcanic rocks in easten China.Compositional comparisons between whole rocks and glasses of various occurrences indicate that the magma tends to become rich in silica and alkalis as a result of crystal differentiation in the course of evolu-tion.They are unique in isotopic composition with more radiogenic Sr but less radiogenic Pb.^87Sr/^86Sr is higher and ^143Nd/^144Nd is lower than the undifferentiated global values.In comparison to continental pot-ash volcanic rocks,Pb isotopes are apparently lower.These various threads of evidence indicate that the rocks were derived from a primary enriched mantle which had not been subjected to reworking and shows no sign of incorporation of crustal material.The correlation between Pb and Sr suggests the regional heterogeneity in the upper mantle in terms of chemical composition. 相似文献
Helium, Sr, and Nd isotopic ratios and major and trace element compositions have been measured on a suite of lavas from the intra-plate volcanos of the Juan Fernandez Archipelago, Chile. Lavas from the islands of Mas Afuera and Mas a Tierra and from Monte Alpha and Friday seamounts have Sr and Nd isotopic ratios lying on the low143Nd/144Nd side of the mantle array (87Sr/86Sr:0.7034–0.7037;143Nd/144Nd:0.51281–0.51289). The homogeneity of these tracers suggests the involvement of a restricted range of mantle source compositions throughout Juan Fernandez volcanism. In marked contrast is the large range in3He/4He, from 7.8 to 18.0 RA. A bimodal3He/4He distribution on Mas a Tierra is associated with two distinct volcanic lineages;3He/4He ratios of 14.5–18.0 RA (n=15) occur in alkalic and tholeiitic shield basalts, whereas post-shield basanites range from 11.2 to 13.6 RA (n=12). Elemental and isotopic systematics demonstrate a transition from an enriched (Loihi-like) plume source in the shield lavas to a more MORB-like source in the post-shield volcanics. The transition between these sources is much more pronounced in3He/4He than in the other isotopic tracers. The predominantly tholeiitic basalts of Mas Afuera have exceptionally uniform isotopic and elemental characteristics; Sr and Nd ratios are similar to those of Mas a Tierra, but3He/4He ratios are lower and more uniform at 8.3±0.5 RA (n=17). The dramatic distinction between Mas Afuera and Mas a Tierra helium is surprising given the great similarity between the two islands in other geochemical characteristics. Both the Mas Afuera and Mas a Tierra results demonstrate that helium records systematic processes not readily apparent from other isotopic or elemental indicators. Neither magma chamber degassing nor local metasomatic events are likely to be responsible. We suggest that the observed variations may be attributed to mixing of plume and asthenospheric sources in which the plume component is characterized by a heterogeneous distribution of volatiles or has suffered extraction of small degree partial melts prior to mixing. 相似文献
Major- and rare-earth-element (REE) concentrations and UThPb, SmNd, and RbSr isotope systematics are reported for Cenozoic volcanic rocks from northeastern and eastern China. These volcanic rocks, characteristically lacking the calc-alkaline suite of orogenic belts, were emplaced in a rift system which formed in response to the subduction of the western Pacific plate beneath the eastern Asiatic continental margin. The rocks sampled range from basanite and alkali olivine basalt, through olivine tholeiite and quartz tholeiite, to potassic basalts, alkali trachytes, pantellerite, and limburgite. These rock suites represent the volcanic centers of Datong, Hanobar, Kuandian, Changbaishan and Wudalianchi in northeastern China, and Mingxi in the Fujian Province of eastern China.The major-element and REE geochemistry is characteristic of each volcanic suite broadly evolving through cogenetic magmatic processes. Some of the outstanding features of the isotopic correlation arrays are as follows: (1) NdSr shows an anticorrelation within the field of ocean island basalts, extending from the MORB end-member to an enriched, time-averaged high Rb/Sr and Nd/Sr end-member (EM1), (2) SrPb also shows an anticorrelation, similar to that of Hawaiian and walvis Ridge basalts, (3) NdPb shows a positive correlation, and (4) the 207Pb/204Pb vs 206Pb/204Pb plot shows linear arrays parallel to the general trend (NHRL) for MORB on both sides of the geochron, although in the 208Pb/204Pb vs 206Pb/204Pb plot the linear array is significantly displaced above the NHRL in a pattern similar to that of the oceanic island basalts that show the Dupal signatures. In all isotope correlation patterns, the data arrays define two different mantle components—a MORB-like component and an enriched mantle component. The isotopic data presented here clearly demonstrate the existence of Dupal compositions in the sources of the continental volcanic rocks of eastern China. We suggest that the subcontinental mantle beneath eastern China served as the reservoir for the EMI component, and that the MORB component was either introduced by subduction of the Kula-Pacific Ridge beneath the Asiatic plate in the Late Cretaceous, as proposed by Uyeda and Miyashiro, or by upwellings in the subcontinental asthenosphere due to subduction. 相似文献
We have modeled the distribution of nine toxic metals in the surface sediments from 163 stations in the Venice lagoon using published data. Three entrances from the Adriatic Sea control the circulation in the lagoon and divide it into three basins. We assume, for purposes of modeling, that Porto Marghera at the head of the Industrial Zone area is the single source of toxic metals in the Venice lagoon. In a standing body of lagoon water, concentration of pollutants at distancex from the source (C0) may be given byC=C0e–kx wherek is the rate constant of dispersal. We calculatedk empirically using concentrations at the source, and those farthest from it, that is the end points of the lagoon. Averagek values (ppm/km) in the lagoon are: Zn 0.165, Cd 0.116, Hg 0.110, Cu 0.105, Co 0.072, Pb 0.058, Ni 0.008, Cr (0.011) and Fe (0.018 percent/km), and they have complex distributions. Given thek values, concentration at source (C0), and the distancex of any point in the lagoon from the source, we have calculated the model concentrations of the nine metals at each sampling station. Tides, currents, floor morphology, additional sources, and continued dumping perturb model distributions causing anomalies (observed minus model concentrations). Positive anomalies are found near the source, where continued dumping perturbs initial boundary conditions, and in areas of sluggish circulation. Negative anomalies are found in areas with strong currents that may flush sediments out of the lagoon. We have thus identified areas in the lagoon where higher rate of sediment removal and exchange may lessen pollution. 相似文献