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1.
In 140 metres of Maastrichtian White Chalk (nannofossil chalk) exposed near Hemmoor, NW Germany, values of 87Sr/86Sr increase from 0.707760 in the Belemnella sumensis Zone (Lower Maastrichtian) at the base of the section (-54.5 m; referred to 0 m at a prominent marl, M900) to 0.707821 in the Belemnella baltica/danica Zone (Upper Maastrichtian) at the top of the section (+84.5 m). A plateau in 87Sr/86Sr occurs between -5m and +50m in the section, probably as a result of a very high rate of sedimentation in this interval. A belemnite and associated nannofossil chalk have similar 87Sr/86Sr values, suggesting that there has been little diagenetic alteration of the 87Sr/86Sr ratios in the chalk, which therefore preserves its original 87Sr/86Sr. Comparison of 87Sr/86Sr and nannofossil zonations for sequences at Bidart, France, and DSDP Sites reveals discordance and so possible diachronism of the basal boundaries of nannofossil Zones CC25B and CC25C.  相似文献   

2.
We have measured 87Sr/86Sr and 143 Nd/144 Nd isotope ratios in different batches and aliquots of the new US Geological Survey (USGS) reference materials (RMs) BCR-2, BHVO-2, AGV-2 and GSP-2 and the original USGS RMs BCR-1, BHVO-1, AGV-1 and GSP-1 by thermal ionisation mass spectrometry. In addition, we also analysed the eight Max-Planck-Institut-Dingwell (MPI-DING) reference glasses. Nearly all isotope ratios obtained in the different aliquots and batches agree within uncertainty limits indicating excellent homogeneity of the USGS powders and the MPI-DING glasses. With the exception of GSP-2, the new USGS RMs are also indistinguishable from the ratios found in the original USGS RMs (87Sr/86Sr: 0.704960, 0.704958 (BCR-1, -2), 0.703436, 0.703435 (BHVO-1, -2), 0.703931, 0.703931 (AGV-1, -2); 143 Nd/144 Nd: 0.512629, 0.512633 (BCR-1, -2), 0.512957, 0.512957 (BHVO-1, -2); 0.512758, 0.512755 (AGV-1, -2)). This means that for normalisation purposes in Sr and Nd isotope geochemistry BCR-2, BHVO-2 and AGV-2 can well replace BCR-1, BHVO-1 and AGV-1 respectively.  相似文献   

3.
Najman  Bickle  & Chapman 《地学学报》2000,12(1):28-34
Nd- and Sr-isotopic compositions of Palaeogene foreland basin sediments are used to provide insights into early Himalayan evolution, particularly the timing of exposure of high 87Sr/86Sr units, erosion of which may have caused the late Tertiary increase in oceanic Sr-isotopic ratios. During the late Palaeocene–early Eocene, erosion was from mixed sources including suture zone rocks. Exhumation of the High Himalaya was occurring by the time of deposition of alluvial sediments after mid-Oligocene times and this source has dominated Himalayan sediments from at least this time until the present day. The transition is interpreted to reflect exhumation of 'basement rocks' of the Indian plate, when the High Himalaya became a sufficient topographic barrier to separate suture zone rocks from the foreland basin. The marked rise in seawater 87Sr/86Sr from 40 Ma is consistent with the erosion of a Himalayan source with a high 87Sr/86Sr ratio.  相似文献   

4.
ABSTRACT This work presents a detailed 87Sr/86Sr isotope curve for the interval 7.5–9.7 Ma obtained by a high-resolution analysis (sampling spacing of about 40 kyr) of an astronomically calibrated land-based sedimentary sequence exposed in the central Mediterranean area (Gibliscemi section, southern Sicily). The main aim is to verify a synchronous response of the Mediterranean seawater Sr isotope record to the oceanic forcing on the basis of multiple comparisons of the Gibliscemi record with published coeval 87Sr/86Sr curves. A good correlation with the 87Sr/86Sr data from the ODP site 926 (equatorial Atlantic ocean), considered to be the Sr chemostratigraphic reference section for the Late Miocene, and from the Pacific DSDP site 590B was registered. Conversely, the comparison of the Gibliscemi Sr isotope data with 87Sr/86Sr ratios from the coeval segment of the land-based Sardella section (eastern Mediterranean) shows important differences highlighting a local control on the seawater Sr isotope changes in semi-isolated subbasins within the Late Miocene Mediterranean.  相似文献   

5.
Garnet peridotites occur as lenses, blocks or layers within granulite–amphibolite facies gneiss in the Dabie-Sulu ultra-high-pressure (UHP) terrane and contain coesite-bearing eclogite. Two distinct types of garnet peridotite were identified based on mode of occurrence and petrochemical characteristics. Type A mantle-derived peridotites originated from either: (1) the mantle wedge above a subduction zone, (2) the footwall mantle of the subducted slab, or (3) were ancient mantle fragments emplaced at crustal depths prior to UHP metamorphism, whereas type B crustal peridotite and pyroxenite are a portion of mafic–ultramafic complexes that were intruded into the continental crust as magmas prior to subduction. Most type A peridotites were derived from a depleted mantle and exhibit petrochemical characteristics of mantle rocks; however, Sr and Nd isotope compositions of some peridotites have been modified by crustal contamination during subduction and/or exhumation. Type B peridotite and pyroxenite show cumulate structure, and some have experienced crustal metasomatism and contamination documented by high 87Sr/86Sr ratios (0.707–0.708), low εNd( t ) values (−6 to −9) and low δ18O values of minerals (+2.92 to +4.52). Garnet peridotites of both types experienced multi-stage recrystallization; some of them record prograde histories. High- P–T  estimates (760–970 °C and 4.0–6.5±0.2 GPa) of peak metamorphism indicate that both mantle-derived and crustal ultramafic rocks were subducted to profound depths >100 km (the deepest may be ≥180–200 km) and experienced UHP metamorphism in a subduction zone with an extremely low geothermal gradient of <5 °C km−1.  相似文献   

6.
This compilation report describes the field location, mineralogy, preparation and homogeneity testing of two new GIT-IWG reference materials: Whin Sill dolerite (WS-E) from England and Pitscurrie microgabbro (PM-S) from Scotland. The elemental composition of these two new reference materials has been established by an international cooperative analysis programme involving participation by 104 laboratories. A full assessment of these analytical results is presented, from which working values have been derived for the major elements as well as for 45 trace elements in WS-E and 44 trace elements in PM-S. Furthermore, isotopic ratios are presented for both samples, particularly for 87Sr/86Sr and 143Nd/144Nd.  相似文献   

7.
Abstract. The Jecheon granitoids, having an elongated shape of NE-SW 27 km and NW-SE 13 km (190 km2), are composed mostly of magnetite-series hornblende-biotite granodiorite and biotite granite, which intrude into the Neoproterozoic metamor-phic and Paleozoic sedimentary rocks of the Ogcheon Belt. The granitoids have Triassic-Jurassic age of 202.7 ±1.9 Ma with very high 87Sr/86Sr initial ratio of 0.7140. The granodiorite has 63–69 % SiO2, 15.1–17.3 % Al2O3, <1.6 % MgO, 6–15 ppm Y and Sr/Y ratios of 24–76, and is depleted in HREE. Biotite granite together, the Jecheon pluton has adakitic characteristics, which are unique in a continental tectonic setting. The granitoids may have been generated by partial melting of an older adakitic granitoid of I-type basement, or by separation of early crystallized garnet and hornblende from an anatectic melt.  相似文献   

8.
In the Boreal Chalk of northwestern Europe the base of the Maastrichtian Stage is defined by entry of the belemnite Belemnella . In the Kronsmoor section, in northwestern Germany, which is a standard section for the European Chalk, 87Sr/86Sr at the Campanian/ Maastrichtian (C/M) boundary is 0.707723±9 (10). An isotopic correlation of this boundary to the US Western Interior, for which a highly refined cephalopod biostratigraphy exists, suggests that this boundary, as defined at Kronsmoor, occurs within the Baculites jenseni zone. This correlationagrees with the latest placement based on biostratigraphic criteria. On87Sr/86Srcriteria the boundary at Kronsmoor correlates to the English Chalk at Trunch, Norfolk, UK, at a level 3.5 m lower than its position based on biostratigraphic criteria.
At Kronsmoor, 87Sr/86Sr increases in a quasi-linear manner through much of the section, suggesting that, averaged over intervals of 1 Myr, the gross sedimentation rate and temporal rate of change of 87Sr/86Sr were approximately constant through the section. For US samples, zonally-plotted values of 87Sr/86Sr define a quasi-linear trend, which suggests a moderate uniformity of zonal duration from the Baculites compressus zone (73.2±0.7 Ma, 10) to the Baculites grandis zone (70.1±0.7 Ma, 10).  相似文献   

9.
Abstract The Rand and Pelona Schists consist of eugeoclinal rock types overlain by continental basement along the Vincent-Chocolate Mountains (VCM) faults. Both schists display inverted metamorphic zonation, defined in part by a systematic variation in composition of calcic to sodic-calcic amphibole in mafic schist structurally upward. The compositional progressions include increase of total A1, A1IV and Ti, but decrease in the ratios of Na/(Na + Ca) to A1/(A1 + Si), and NaM4 to (A1VI+ Fe3++ Ti). These variations imply that structurally high rocks belong to a lower-pressure metamorphic fades series than those at depth. This result is consistent with previous views that the inverted metamorphic zonations represent intact structural sequences.
Amphibole composition is dependent not only on structural position (i.e. P-T ), but also upon bulk-rock composition. The important controls are whole-rock Mg/(Mg + Fe2++ Mn) and Fe3+/Fe2+. The greatest impact of these factors, however, is on the absolute values of Na and Al, rather than their ratio. Thus, interpretation of facies series is not seriously hindered by compositional variability.
Sodic amphibole in epidote blueschists from the Rand Schist is extensively replaced by sodic-calcic amphibole. Sodic-calcic amphibole in the Rand Schist and Pelona Schist is, itself, rimmed by actinolitic amphibole. Similar blueschist to greenschist transitions in other metamorphic terranes are typically attributed to exhumation. In the Rand and Pelona Schists, the sequence probably formed during burial.  相似文献   

10.
An igneous zircon reference material (OG1) was characterised for U-Pb isotopes by ID-TIMS, and utilised to evaluate SIMS (SHRIMP) instrumental mass fractionation (IMF) of radiogenic Pb isotopes (207Pb*/206Pb*). The TIMS 207Pb*/206Pb* reference value for OG1 was 0.29907 ± 0.00011 (95% confidence limit), 3465.4 ± 0.6 Ma. The high 207Pb* (∼ 30 μg g−1), negligible common Pb, and isotopic homogeneity permitted precise (± 1–2‰) 207Pb*/206Pb* measurements within the analytical sessions. External reproducibility of mean 207Pb*/206Pb* ratios between sessions was demonstrated for one instrument, yielding a mean IMF of +0.87 ± 0.49‰. The mean 207Pb*/206Pb* ratios between instruments were dispersed beyond uncertainties, with session IMF values from +3.6 ± 1.7‰ to −2.4 ± 1.3‰, and a grand mean IMF value (twenty-six sessions) of +0.70 ± 0.52‰, indicating a tendency towards elevated 207Pb*/206Pb*. The specific causes of variability in IMF are unclear, but generally reflect subtle differences in analytical conditions. The common practice in SIMS of assuming that IMF for Pb+ is insignificant could result in systematic age biases and underestimated uncertainties, of critical importance for precise correlation of Precambrian events. Nevertheless, a zircon RM such as OG1 can be readily incorporated into routine dating to improve 207Pb*/206Pb* accuracy and external reproducibility.  相似文献   

11.
The geochemistry of Re-Os and the recent use of Re as a non-traditional stable isotope both need accurate and precise quantification of 187Re/185Re ratios. This paper reports rhenium isotopic data obtained from the analysis of a standard solution and geological samples by MC-ICP-MS. We show that measured isotopic ratios are modified by matrix effects that cannot be accounted for by the standard solution bracketing technique. The bias resulting from measurements on a spiked (185Re-enriched) sample is shown to alter the apparent Re concentration by several percent. When spiking samples and calibrators with tungsten, simultaneous measurement of tungsten and rhenium isotopes compensates for the matrix-induced modification of mass bias. Rhenium and tungsten are shown to have different fractionation factors. This may be due to the fact that the two elements fractionate in a different but systematic way, or that the reference isotopic ratios used for elemental Re and W are incoherent with one another. The consistency of fractionation through time can be used to obtain an empirical relationship between W and Re measured ratios from a standard solution to obtain a sample's fractionation-corrected 187Re/185Re spiked ratio on samples containing pg g−1 levels of Re, even if some matrix capable of affecting mass bias remains in the final solution.  相似文献   

12.
Hamidi  Nahon  McKenzie  Michard  Colin  & Kamel 《地学学报》1999,11(4):157-161
Carbonate commonly accumulates in weathering profiles developed on noncalcareous parent material under arid and semiarid climatic conditions. Such weathering profile types are widespread in Morocco, making it critical to know the sources of the calcium in order to understand the genesis of carbonate-rich soils. In this study, we use 87Sr/86Sr as a geochemical tracer of the Ca sources in weathering profiles developed on volcanic rocks (basalt, tuff, andesite and latite) in the Mediterranean coast of Morocco. The results show that the most of the Sr, and hence Ca, is of an external origin, derived from (i) sea-water for the profiles located near to the coast or (ii) sea-water plus Liassic carbonate outcropping in the catchment for the profiles more distant from the coastline. The contribution of the host rock is small, being less than 25%. The ratio of the Sr (Ca) from the parent material to that from the external sources is controlled by the degree of porosity developed in the profile.  相似文献   

13.
Sr-isotope measurements of unaltered oyster shell calcite using laser-ablation multi-collector ICPMS techniques represent a powerful tool capable of establishing a chronostratigraphic framework for fossil near-shore deposits. This approach is tested on two shoal-water successions from the Portuguese Algarve and Lusitanian basins covering Late Barremian to Albian strata. 87Sr/86Sr values derived from low-Mg calcite of oyster shells fluctuate between 0.70717 ± 0.00001 and 0.70746 ± 0.00002; absolute values as well as stratigraphic trends match well with the global open-marine seawater signal. The new Sr-isotope results in combination with existing bio- and chemostratigraphic records allow for identification of an Early Aptian biocalcification crisis at both studied localities and show that this event has severely affected coastal environments along the evolving Atlantic. Siliciclastic intervals in the Algarve section are interpreted as near-shore equivalents of enhanced detrital shedding into shelf and deep-sea environments as a consequence of increased chemical weathering rates during humid climate episodes.  相似文献   

14.
The Holocene San Quintín volcanic province in northern Baja California comprises spinel-lherzolite-bearing alkali basalts. Trace element (La/Nb = 0.57–0.73; K/Rb = 402–479; LaN/YbN= 8.4, 9.9) and isotopic ratios (87Sr/86r = 0.70323–0.70352; 143Nd/144Nd = 0.512924–0.512996; 206Pb/204Pb = 19.108, 19.250; 207Pb/204Pb = 15.567, 15.589; 208Pb/204Pb = 38.82, 38.85) show that the lavas are compositionally indistinguishable from some ocean island, plume-associated basalts such as Hawaii and the Azores, and testify to an asthenospheric source for the magmas. The occurrence in Baja of such lavas may be related to the nature of the cessation of plate subduction beneath the peninsula; at present, San Quintín (and volcanic provinces to the north) are underlain by a 'no-slab window', whereas immediately to the south, remanent oceanic lithosphere may be preserved as a relict slab. This may act as a bamer to the upward passage of diapirs or magmas from the asthenosphere.  相似文献   

15.
Zachariah 《地学学报》1998,10(6):312-316
A marble band in the ≈ 2.75 Gyr old Ramagiri schist belt in the Dharwar craton of south India gave a Pb–Pb age of 3.075 ± 0.095 Gyr. The geochemical data, including high Sr and low Ba and Mn indicate seawater origin for the parent rock, and that there was insignificant geochemical exchange between the marble and the surrounding rocks. The calculated initial Nd isotopic composition and μ1 indicate an older continental crustal source for the Nd and Pb. The initial 87Sr/86Sr of the marble is 0.70128, which is higher than the calculated mantle value at ≈ 3 Ga. Although pre-3 Gyr old marine carbonate rocks are thought to be buffered by mantle Sr, the Ramagiri marble contains evolved, crustal Sr. Despite this, the marble has the lowest measured 87Sr/86Sr among carbonates and represents one of the least radiogenic periods in seawater Sr isotope composition.  相似文献   

16.
M.J. Bickle 《地学学报》1996,8(3):270-276
The seawater 87Sr/86Sr curve implies a 50–100 Myr episodicity in weathering rate which requires a corresponding variation in CO2 degassing from the solid earth to the atmosphere. It is proposed that this is caused by orogenesis, which both produces CO2 as a result of metamorphic decarbonation reactions, and consumes extra CO2 as a consequence of erosion-enhanced weathering. Global climate on the geological time-scale is therefore contTolled by the difference between the relatively large and variable orogenic-moderated degassing and weathering CO2 fluxes.  相似文献   

17.
Abstract: The Biliutai pluton, as the host of a small gold deposit, containing dark-gray enclaves, intruded into the Lower Permian volcanic-sedimentary formations in east Inner Mongolia, China. The host rocks and enclaves formed simultaneously at about 200 Ma (Rb–Sr isochron age with initial 87Sr/86Sr of 0.704). The Nd (T) values for the enclaves (from +4.4 to +4.6) are similar to their host rocks (+3.2 to +4.8), although the values for the host rocks are relatively variable. Both enclaves and host rocks are enriched in large ion lithosphere elements and light rare earth elements but depleted in high field strength elements and heavy rare earth elements. These observations suggest that the magma was produced from subduction-modified mantle sources. The age of the mantle enrichment event, evaluated using depleted mantle Nd model ages, is 0.61 - 0.83 Ga. These geochemical characteristics constrain the metallogeny of the Biliutai pluton, and imply that the ore-forming materials probably were derived from lithospheric mantle.  相似文献   

18.
The Ca isotopic composition of modern seawater has been determined using a 43Ca-48Ca double spike, which was calibrated using a 42Ca/44Ca seawater ratio of 0.30587 ± 0.00026. This ratio was determined from a total evaporation experiment in which the ion beam was measured from the beginning to the end of the emission. With integration of the peak intensities, the fractionation effects can be minimised, since total evaporation of the reservoir cancels out the effect of vapour enrichment in the light isotopes. This experiment avoids the gravimetric uncertainty inherent in the double spike calibration. This calibration allows the precise redetermination of the seawater isotopic composition of Ca. A mean 40Ca/44Ca ratio for two Atlantic water samples of 45.143 (2smean= 0.003) was found. The good reproducibility of the Ca isotope ratios in present seawater and the very strong isotopic homogeneity of Ca in the oceans illustrate the advantage of using seawater as the common standard, with the advantage of decreasing interlaboratory bias.  相似文献   

19.
Abstract: Transportation of various kinds of elements occurred in wall rocks (Quaternary andesites) during the hydrothermal alteration accompanied by the Hishikari epithermal gold mineralization. For example, K2O and MgO contents of wall rocks decrease away from the gold-quartz veins, while (CaO+Na2O) content increases, and SiO2 content is variable near the veins. Hydrothermal alteration zoning and bulk compositional variations in wall rocks suggest that the mixing of hydrothermal solution and acidic groundwater took place an important role as the cause for the hydrothermal alteration and bulk compositional variations. The relationship between dissolved silica concentration and temperature of hydrothermal solution mixed with groundwater is obtained based on precipitation kinetics-fluid flow–mixing model, and the computed results are compared with the distribution of SiO2 minerals (quartz and cristobalite) in the hydrothermal alteration zones. This comparison suggests that the most reasonable flow rate of fluids migrating through hydrothermal alteration zones, and A/M (A: surface area of rocks interacting with fluid, M: mass of fluid) are estimated to be ca. 10-4.2 m/sec, and ca. 0.10 m2/kg, respectively. The mixing of two fluids (hydrothermal solution and acidic groundwater) can also explain δ18O zoning in the altered country rocks, hydrothermal alteration zoning from K-feldspar through K-mica to kaolinite from the center (veins) to margin, and deposition of gold.  相似文献   

20.
We present boron isotope and concentration data from magmatic (komatiitic to rhyolitic) and sedimentary geological silicate and artificial glass reference materials that cover a wide spectrum of boron isotope compositions and boron concentrations. Boron isotope compositions were determined by TIMS (Cs2BO2+ -graphite and BO2- method) and boron concentrations by ICP-AES. Boron concentrations ranged from 7 to 159μ g-1 and agree within 14% with published values. Based on replicate analyses of individually prepared sample aliquots an overall external reproducibility of better than 10% was determined. The obtained δ11B values ranged from -12.6 to +13.6% and were reproducible within 1.1 % (2 RSD; excluding NTIMS) on the basis of individually prepared sample aliquots. The δ11B values of JA-1 (+5.3%), JB-3 (+5.9%) and JR-2 (+2.9%) overlap the published data within analytical uncertainty. For the first time δ11B values for the TB (-12.6%) and the MPI-DING glasses GOR-128-G (+13.6%), GOR-132-G (+7.1 %) and StHs6/80-G (-4.5%) are reported. The δ11B values obtained by the Cs2BO2+ -graphite and the BO2- method as well as the majority of δ11B values obtained using different sample preparation methods agree within analytical uncertainty. Therefore, we conclude that none of these analytical methods introduce any systematic error on the obtained δ11B values.  相似文献   

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