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1.
Mixed marine, brackish-water and terrestrial vertebrate skeletal apatite is found in the late Paleocene-early Eocene Tuscahoma and Bashi Formations of Mississippi. The co-Occurrence in these near-coastal marine deposits of skeletal apatite with different provenances offers a unique opportunity for unraveling the effects of diagenesis on apatite 87Sr/86Sr composition, with bearings on the use of this isotope pair as paleosalinity indicator. The results show that the Sr isotopes of all originally poorly ordered phases of skeletal apatite have extensively re-equilibrated with pore water with significantly lower 87Sr/86Sr ratios than late Paleocene-early Eocene seawater. For example, marine shark and ray teeth from the Bashi Formation all have clearly nonmarine 87Sr/86Sr ratios, 0.7073-0.7075, compared with a coeval seawater ratio in the range 0.7077-0.7078. However, separated shark tooth enamel, with a high original crystallinity, appears to have retained all or most of its in vivo Sr isotopic signature until the present. Here we also show that 87Sr/86Sr results on recent vertebrate skeletal material from different environments are in good agreement with expected values for respective habitat.

Earlier analyses of calcite material from the Bashi Formation indicated the existence of a shift in seawater 87Sr/86Sr to a lower value at the Paleocene-Eocene boundary. The strong influence of pore water with low, nonmarine 87Sr/86Sr on the apatite in the Bashi Formation suggests that the proposed isotopic shift may be an artifact related to diagenetic processes.  相似文献   


2.
Three types of chemically and isotopically distinct pore fluids from the southern San Joaquin basin previously recognized by J.B. Fisher and J.R. Boles also have distinctive 87Sr/86Sr ratios and Sr concentrations. Meteoric fluids have stable isotopic compositions which lie on or near the meteoric water line and low chlorinities. Sr concentrations are between 0.01 and 2.6 mg l−1, and 87Sr/86Sr ratios range from 0.7061 to 0.7078. Diagenetically modified connate marine fluids have δD-and δ18O-values more positive than −35‰ and 0‰, respectively, and have chlorinities generally comparable to seawater. Sr concentration are much higher than the meteoric group (16–198 mg l−1), although the 87Sr/86Sr ratios (0.7070–0.7081) are not distinctive. Mixed meteoric-modified connate fluids have δD, δ18O and chlorinity intermediate between the meteoric and modified connate groups. Sr concentrations are also intermediate, between 16 and 22 mg l−1, but 87Sr/86Sr ratios (0.7080–0.7087) are generally more radiogenic than either the meteoric or modified connate groups.

All of the fluids have 87Sr/86Sr ratios comparable to or lower than Tertiary seawater. Alteration of detrital plagioclase is the probable origin of the low isotopic ratios. Mass-balance calculations based on the Sr data suggest that essentially no transport of Sr occurred during diagenesis of sandstones containing modified connate pore fluids, while large amounts of Sr have been transported out of meteoric reservoirs by fluid flow. The chemically anomalous mixed meteoric-modified connate fluids contain the most radiogenic strontium in the basin. These fluids are spatially associated with major faults, and may represent clay mineral dehydration waters which have been transported upward from greater depth.

These results suggest that the three types of fluids identified by Fisher and Boles represent three distinct mass transport regimes: a largely stagnant deep-basin system containing modified connate pore fluids; an actively recharging meteoric system along the basin flanks; and a third system restricted to the southern basin which may be characterized by largescale cross-formational fluid flow, rather than dilution by meteoric waters.  相似文献   


3.
Temporal variation of dissolved 87Sr/86Sr in the Yangtze River is poorly understood compared to other Tibetan rivers. In this study, dissolved Sr and 87Sr/86Sr were measured from a temporal series of water samples collected biweekly at Datong Hydrological Station over a period of one year. Our results show that Sr concentration in the Yangtze River ranges from 1.74 to 2.92 μmol/L with 87Sr/86Sr of 0.710125 to 0.710965. The Sr concentration and 87Sr/86Sr shows a distinct seasonal variation, with a general increase in 87Sr/86Sr ratios from summer to winter and some fluctuations during July and December, then followed by a gradually decrease till the next rainy season. The seasonal variation results from the variation of contributions from different sub-basin due to the spatially and seasonally variable rainfall across the basin. During the flood season, more contribution from upper reach (low 87Sr/86Sr values) due to the strong rainfall decreases the 87Sr/86Sr ratio at lower reach. While the severe drought which happened in the middle-lower reaches (high 87Sr/86Sr values) from January to May explains the decrease in the later part of the data by the decrease of the contribution from middle-lower reaches. The discharge weighted annual 87Sr/86Sr and annual Sr flux of the Yangtze River based on the time series data are 0.710628 and 1.9×109 mol/a, respectively. It was also indicated that dissolved 87Sr/86Sr in the Yangtze River is well correlated to the extreme climate events and might contribute to our explanation for reconstructing past climatic changes by using 87Sr/86Sr ratios of the sedimentary record in the delta .  相似文献   

4.
In order to provide mantle and crustal constraints during the evolution of the Colombian Andes, Sr and Nd isotopic studies were performed in xenoliths from the Mercaderes region, Northern Volcanic Zone, Colombia. Xenoliths are found in the Granatifera Tuff, a deposit of Cenozoic age, in which mantle- and crustal-derived xenoliths are present in bombs and fragments of andesites and lamprophyres compositions. Garnet-bearing xenoliths are the most abundant mantle-derived rocks, but websterites (garnet-free xenoliths) and spinel-bearing peridotites are also present in minor amounts. Amphibolites, pyroxenites, granulites, and gneisses represent the lower crustal xenolith assemblage. Isotopic signatures for the mantle xenoliths, together with field, petrographic, mineral, and whole-rock chemistry and pressure–temperature estimates, suggest three main sources for these mantle xenoliths: garnet-free websterite xenoliths derived from a source region with low P and T (16 kbar, 1065 °C) and MORB isotopic signature, 87Sr/86Sr ratio of 0.7030, and 143Nd/144Nd ratio of 0.5129. Garnet-bearing peridotite and websterite xenoliths derived from two different sources in the mantle: i) a source with intermediate P and T (29–35 kbar, 1250–1295 °C) conditions, similar to that of sub-oceanic geotherm, with an OIB isotopic signature (87Sr/86Sr ratio of 0.7043 and 143Nd/144Nd ratio of 0.5129); and ii) another source with P and T conditions similar to those of a sub-continental geotherm (>38 kbar, 1140–1175 °C) and OIB isotopic characteristics (87Sr/86Sr ratio=0.7041 and 143Nd/144Nd ratio=0.5135).  相似文献   

5.
S. Jung   《Lithos》2005,84(3-4):168-184
The overwhelming part of the continental crust in the high-grade part of the Damara orogen of Namibia consists of S-type granites, metasedimentary rocks and migmatites. At Oetmoed (central Damara orogen) two different S-type granites occur. Their negative εNd values (− 3.3 to − 5.9), moderately high initial 87Sr/86Sr ratios (0.714–0.731), moderately high 206Pb/204Pb (18.21–18.70) and 208Pb/204Pb (37.74–37.89) isotope ratios suggest that they originated by melting of mainly mid-Proterozoic metasedimentary material. Metasedimentary country rocks have initial εNd of − 4.2 to − 5.6, initial 87Sr/86Sr of 0.718–0.725, 206Pb/204Pb ratios of 18.32–18.69 and 208Pb/204Pb ratios of 37.91–38.45 compatible with their variation in Rb/Sr, U/Pb and Th/Pb ratios. Some migmatites and residual metasedimentary xenoliths tend to have more variable εNd values (initial εNd: − 4.2 to − 7.1), initial Sr isotope ratios (87Sr/86Sr: 0.708–0.735) and less radiogenic 206Pb/204Pb (18.22–18.53) and 208Pb/204Pb (37.78–38.10) isotope compositions than the metasedimentary rocks. On a Rb–Sr isochron plot the metasedimentary rocks and various migmatites plot on a straight line that corresponds to an age of c. 550 Ma which is interpreted to indicate major fractionation of the Rb–Sr system at that time. However, initial 87Sr/86Sr ratios of the melanosomes of the stromatic migmatites (calculated for their U–Pb monazite and Sm–Nd garnet ages of c. 510 Ma) are more radiogenic (87Sr/86Sr: 0.725) than those obtained on their corresponding leucosomes (87Sr/86Sr: 0.718) implying disequilibrium conditions during migmatization that have not lead to complete homogenization of the Rb–Sr system. However, the leucosomes have similar Nd isotope characteristics than the inferred residues (melanosomes) indicating the robustness of the Sm–Nd isotope system during high-grade metamorphism and melting. On a Rb–Sr isochron plot residual metasedimentary xenoliths show residual slopes of c. 66 Ma (calculated for an U–Pb monazite age of 470 Ma) again indicating major fractionation of Rb/Sr at c. 540 Ma. However, at 540 Ma, these xenoliths have unradiogenic Sr isotope compositions of c. 0.7052, indicating depleted metasedimentary sources at depth. Based on the distinct Pb isotope composition of the metasedimentary rocks and S-type granites, metasedimentary rocks similar to the country rocks are unlikely sources for the S-type granites. Moreover, a combination of Sr, Nd, Pb and O isotopes favours a three-component mixing model (metasedimentary rocks, altered volcanogenic material, meta-igneous crust) that may explain the isotopic variabilty of the granites. The mid-crustal origin of the different types of granite emphasises the importance of recycling and reprocessing of pre-existing differentiated material and precludes a direct mantle contribution during the petrogenesis of the orogenic granites in the central Damara orogen of Namibia.  相似文献   

6.
The hydrochemical interaction between groundwater and lakewater influences the composition of water that percolates downward from the surficial aquifer system through the underlying intermediate confining unit and recharges the Upper Floridan aquifer along highlands in Florida. The 87Sr/86Sr ratio along with the stable isotopes, D, 18O, and 13C were used as tracers to study the interaction between groundwater, lakewater, and aquifer minerals near Lake Barco, a seepage lake in the mantled karst terrane of northern Florida. Upgradient from the lake, the 87Sr/86Sr ratio of groundwater decreases with depth (mean values of 0.71004, 0.70890, and 0.70852 for water from the surficial aquifer system, intermediate confining unit, and Upper Floridan aquifer, respectively), resulting from the interaction of dilute oxygenated recharge water with aquifer minerals that are less radiogenic with depth. The concentrations of Sr2+ generally increase with depth, and higher concentrations of Sr2+ in water from the Upper Floridan aquifer (20–35 μg/L), relative to water from the surficial aquifer system and the intermediate confining unit, result from the dissolution of Sr-bearing calcite and dolomite in the Eocene limestone. Dissolution of calcite [δ13C = −1.6 permil (%o)] is also indicated by an enriched δ13CDIC(-8.8 to -11.4% o) in water from the Upper Floridan aquifer, relative to the overlying hydrogeologic units (δ13CDIC < -16%o).

Groundwater downgradient from Lake Barco was enriched in 18O and D relative to groundwater upgradient from the lake, indicating mixing of lakewater leakage and groundwater. Downgradient from the lake, the 87Sr/86Sr ratio of groundwater and aquifer material become less radiogenic and the Sr2+ concentrations generally increase with depth. However, Sr2+ concentrations are substantially less than in upgradient groundwaters at similar depths. The lower Sr2+ concentrations result from the influence of anoxic lakewater leakage on the mobility of Sr2+ from clays. Based on results from mass-balance modeling, it is probable that cation exchange plays the dominant role in controlling the 87Sr/86Sr ratio of groundwater, both upgradient and downgradient from Lake Barco. Even though groundwater from the three distinct hydrogeologic units displays considerable variability in Sr concentration and isotopic composition, the dominant processes associated with the mixing of lakewater leakage with groundwater, as well as the effects of mineral-water interaction, can be ascertained by integrating the use of stable and radiogenic isotopic measurements of groundwater, lakewater, and aquifer minerals.  相似文献   


7.
C.J. Adams  R.J. Beck  H.J. Campbell   《Lithos》2007,97(3-4):307-322
Nephrite jade occurs in three terranes (Dun Mountain–Maitai, Caples and Torlesse) in New Zealand, where it is associated with ultramafic and ophiolitic rocks in narrow metasomatic reaction zones at the margins of serpentinite (having harzburgite/gabbro/dolerite precursors) with silicic metasediments and metavolcanics. True nephrite fabrics are developed only locally where marginal shearing is intense, and late in the metamorphic history. 87Sr/86Sr values of these nephrites do not display the primitive values of their gabbro/dolerite precursor component i.e. 0.7030–0.7035, as expected if formed during serpentinisation. Rather, the nephrites have more evolved 87Sr/86Sr values inherited from the metasediment component at a later stage, and which fall within particular terrane groups: Dun Mountain–Maitai 0.7045–0.7060, Caples 0.7058–0.7075 and Torlesse 0.7085–0.7110. Rb–Sr ages and initial 87Sr/86Sr ratios of the metasediment component from in situ nephrite localities, when compared with their counterparts throughout the host terrane, show that nephrite Sr isotopic compositions are characteristic of the host terrane.  相似文献   

8.
Sr isotope and Ca/Mg/Sr chemical compositions of freshwater ostracode tests separated from a sediment core represent the last 16 ka of sedimentation in Lake Constance, Central Europe. The chemical evolution of the paleowater's dissolved load of Lake Constance was estimated by correcting the ostracode data for Ca/Mg/Sr fractionation due to biogenic calcification. Since the Late Pleistocene deglaciation, the Ca/Sr molar ratios of paleowaters increased systematically from about 100 (a near marine signature) to about 200. Ca/Mg molar ratios varied in the range of 1–25. The 87Sr/86Sr ratios indicate Late Pleistocene paleowater compositions of 0.7086–0.7091, significantly more radiogenic than present day waters (0.7085). Sr isotopes and Ca/Mg/Sr chemical data together show that weathering of Mesozoic evaporites consistently dominated the dissolved Sr load (80–90%). Carbonate and silicate weathering were less important (1–10%). Trends of Sr dissolved loads were therefore not related to Mg which was mainly mobilized by carbonate weathering. Biotite weathering was an important source of radiogenic Sr in the paleowaters. The short-term release (duration about 600–800 years) of radiogenic Sr during glacier retreat started 15.2 ka ago and was due to enhanced biotite weathering at the glacier base. Long-term release of radiogenic Sr was due to biotite weathering in glacial soils and silicate rocks, and has gradually declined since the Late Pleistocene/Holocene transition.  相似文献   

9.
The Sr, Nd and Pb isotopic compositions for the Kovdor phoscorite–carbonatite complex (PCC), Kola Peninsula, NW Russia, have been determined to characterize the mantle sources involved and to evaluate the relative contributions of a plume and subcontinental lithospheric mantle in the formation of the complex. The Kovdor PCC is a part of the Kovdor ultramafic–alkaline–carbonatite massif, and consists of six intrusions. The initial isotopic ratios of the analyzed samples, calculated at 380 Ma, display limited variations: εNd, + 2.0 to + 4.7; 87Sr/86Sr, 0.70319 to 0.70361 (εSr, − 12.2 to − 6.2); 206Pb/204Pb, 18.38 to 18.74; 207Pb/204Pb, 15.45 to 15.50; 208Pb/204Pb, 37.98 to 39.28. The Nd and Sr isotope data of the Kovdor PCC generally fit the patterns of the other phoscorites and carbonatites from the Kola Alkaline Province (KAP), but some data are slightly shifted from the mixing line defined as the Kola Carbonatite Line, having more radiogenic 87Sr/86Sr ratios. However, the less radiogenic Nd isotopic compositions and negative Δ7/4 values of Pb isotopes of the analyzed samples exclude crustal contamination, but imply the involvement of a metasomatized lithospheric mantle source. Isotopic variations indicate mixing of at least three distinct mantle components: FOZO-like primitive plume component, EMI-like enriched component and DMM-like depleted component. The isotopic nature of the EMI- and DMM-like mantle component observed in the Kovdor samples is considered to be inherited from metasomatized subcontinental lithospheric mantle. This supports the previous models invoking plume–lithosphere interaction to explain the origin of the Devonian alkaline carbonatite magmatism in the KAP.  相似文献   

10.
争光金矿床位于兴安地块东缘黑龙江省多宝山铜钼-金矿集区南东端,矿体产于早奥陶世闪长岩与下奥陶统多宝山组地层接触带及多宝山组中,为大型金矿.因缺乏精确的成矿年代学研究,其成矿时代一直存在争议.本文在争光金矿床地质背景和岩石矿物学研究的基础上,对矿区内12件矿石样品中共生矿物方铅矿和黄铁矿进行Rb-Sr同位素年代学研究.结...  相似文献   

11.
The significance of isotopic data on constraining the physical conditions of fluid-rock interaction and mineralization processes in carbonate rocks is discussed, based on the example of barite-tetrahedrite mineralization in Lower Devonian platform carbonates of the Western Greywacke Zone (Tyrol, Austria). Available strontium, oxygen, carbon and sulfur isotopic data are complemented with oxygen isotopic data for barite. Barites are homogeneous in δ18OV-SMOW and δ34SCDT with values of + 15.4 and + 23.5‰, respectively. Their 87Sr/86Sr ratios vary between 0.7128 and 0.7113 for the first generation and between 0.7117 and 0.7123 for younger remobilization. The dolomitic host rock shows a significant variation in Sr, O and C isotopic composition between non-mineralized and mineralized zones: 87Sr/86Sr ratios vary between 0.7076 and 0.7133, δ18OV-SMOW-values between +28.11 and +20.65‰, and δ13CPDB-values between −1.15 and + 3.06‰. Fluid/rock volume ratios on the order of 1.3–3.2 are calculated for open-system behaviour by modelling Sr, O and C isotopic shifting capacities. The isotope data combined with other geological evidence support the following genetic model: Subsequent to synsedimentary sulfide mineralization during an Early Devonian rifting stage, collision tectonics in Carboniferous time led to the expulsion of Ba- and Sr-rich orogenic brines, which evolved from metamorphic fluids consisting essentially of H2O and some CH4, into an external sedimentary fold-and-thrust belt. The brines remobilized the synsedimentary sulfides, mixed with meteoric waters in the platform carbonates, reacted with evaporitic horizons and finally caused the recrystallization of dolomite and the precipitation of Sr-rich barite in structurally weak zones at 70–130°C. During the later Alpine orogeny supergene oxidation products were formed, and sulfates, sulfides and carbonates were further remobilized into late faults and fractures.  相似文献   

12.
Voluminous late Mesoproterozoic monzonite through granite of the Vernon Supersuite underlies an area of approximately 1300 km2 in the Highlands of northern New Jersey. The Vernon Supersuite consists of hastingsite±biotite-bearing granitoids of the Byram Intrusive Suite (BIS) and hedenbergite-bearing granitoids of the Lake Hopatcong Intrusive Suite (LHIS). These rocks have similar major and trace element abundances over a range of SiO2 from 58 to 75 wt.%, are metaluminous to weakly peraluminous, and have a distinctive A-type chemistry characterized by high contents of Y, Nb, Zr, LREE, and Ga/Al ratios, and low MgO, CaO, Sr and HREE. Whole-rock Rb–Sr isochrons of BIS granite yield an age of 1116±41 Ma and initial 87Sr/86Sr ratio of 0.70389, and of LHIS granite an age of 1095±9 Ma and initial 87Sr/86Sr ratio of 0.70520. Both suites have similar initial 143Nd/144Nd ratios of 0.511267 to 0.511345 (BIS) and 0.511359 to 0.511395 (LHIS). Values of Nd are moderately high and range from +1.21 to +2.74 in the BIS and +2.24 to +2.95 in the LHIS. Petrographic evidence, field relationships, geochemistry, and isotopic data support an interpretation of comagmatism and the derivation of both suites from a mantle-derived or a juvenile lower crustal parent with little crustal assimilation. Both suites crystallized under overlapping conditions controlled by P–T–fH2O. Lake Hopatcong magma crystallized at a liquidus temperature that approached 900°C and a pressure of about 6 kbar, and remained relatively anhydrous throughout its evolution. Initial P–T conditions of the Byram magma were ≥850°C and about 5.5 kbar. BIS magma was emplaced contemporaneous with, or slightly preceding LHIS magma, and both magmas were emplaced during a compressional tectonic event prior to granulite facies metamorphism that occurred in the Highlands between 1080 and 1030 Ma.  相似文献   

13.
The Korosten complex is a Paleoproterozoic gabbro–anorthosite–rapakivi granite intrusion which was emplaced over a protracted time interval — 1800–1737 Ma. The complex occupies an area of about 12 000 km2 in the north-western region of the Ukrainian shield. About 18% of this area is occupied by various mafic rocks (gabbro, leucogabbro, anorthosite) that comprise five rock suites: early anorthositic A1 (1800–1780 Ma), main anorthositic A2 (1760 Ma), early gabbroic G3 (between 1760 and 1758 Ma), late gabbroic G4 (1758 Ma), and a suite of dykes D5 (before 1737 Ma). In order to examine the relationships between the various intrusions and to assess possible magmatic sources, Nd and Sr isotopic composition in mafic whole-rock samples were measured. New Sr and Nd isotope measurements combined with literature data for the mafic rocks of the Korosten complex are consistent and enable construction of Rb–Sr and Sm–Nd isochronous regressions that yield the following ages: 1870 ± 310 Ma (Rb–Sr) and 1721 ± 90 Ma (Sm–Nd). These ages are in agreement with those obtained by the U–Pb method on zircons and indicate that both Rb–Sr and Sm–Nd systems have remained closed since the time of crystallisation. In detail, however, measurable differences in isotopic composition of the Korosten mafic rock depending on their suite affiliation were revealed. The oldest, A1 rocks have lower Sr (87Sr/86Sr(1760) = 0.70233–0.70288) and higher Nd (εNd(1760) = 1.6–0.9) isotopic composition. The most widespread A2 anorthosite and leucogabbro display higher Sr and lower Nd isotopic composition: 87Sr/86Sr(1760) = 0.70362, εNd(1760) varies from 0.2 to − 0.7. The G3 gabbro–norite has slightly lower εNd(1760) varying from − 0.7 to − 0.9. Finally, G4 gabbroic rocks show relatively high initial 87Sr/86Sr (0.70334–0.70336) and the lowest Nd isotopic composition (εNd(1760) varies from − 0.8 to − 1.4) of any of the mafic rocks of the Korosten complex studied to date. On the basis of Sr and Nd isotopic composition we conclude that Korosten initial melts may have inherited their Nd and Sr isotopic characteristics from the lower crust created during the 2.05–1.95 Ga Osnitsk orogeny and 2.0 Ga continental flood basalt event. Indeed, εNd(1760) values in Osnitsk rocks vary from 0.0 to − 1.9 and from 0.2 to 3.4 in flood basalts. We suggest that these rocks being drawn into the upper mantle might melt and give rise to the Korosten initial melts. 87Sr/86Sr(1760) values also support this interpretation. We suggest that the Sr and Nd isotopic data currently available on mafic rocks of the Korosten complex are consistent with an origin of its primary melts by partial melting of lower crustal material due to downthrusting of the lower crust into upper mantle forced by Paleoproterozoic amalgamation of Sarmatia and Fennoscandia.  相似文献   

14.
This paper determines the weathering and atmospheric contributions of Ca in surface water from a small spruce forested silicate catchment (N–E France) receiving acid atmospheric inputs. The bedrock is a granite with K-feldspar and albite as dominant phases. The calcium content in plagioclase is low and the Ca/Na ratio in surface water is high, reflecting other sources of calcium from those expected from the weathering of major mineral phases. The biotite content is low. Only traces of apatite were detected while no calcite was found in spite of a major hydrothermal event having affected the granite. The strontium isotopic ratio 87Sr/86Sr and Sr content was used as a tracer of weathering and was determined in minerals and bulk bedrock, open field precipitation, throughfall, soil solution, spring and stream water. The Sr isotopic ratio of the reacting weathering end-member was predicted by simulating the alteration of the granite minerals by incorporating strontium into the water–rock interaction kinetic code KINDIS. In the early stages of water–rock interaction, K-feldspar and biotite strongly influence the isotopic composition of the weathering solution whereas, the Na-rich plagioclase appears to be the main long-term reactive weathering end-member. Approximately 50% of dissolved Sr in streamwater are atmospherically derived. The 87Sr/86Sr ratios of exchangeable Sr in the fine fraction at 1-m depth from a soil profile indicate that the amount of exchangeable Sr seems essentially controlled by atmospheric inputs. The exception is the deep saprolite where weathering processes could supply the Sr (and Ca). Na-Plagioclase weathering obviously control the chemistry and the isotopic composition of surface waters. The weathering of trace mineral plays a secondary role, the exception is for apatite when plagioclase is absent. Our hydrochemical, mineralogical and isotopic investigations show that a major part of the strong Ca losses detected in catchment hydrochemical budgets that result from the neutralization of acid precipitation has an atmospheric origin. Consequently, in the long term, in such areas, the availability of such an exchangeable base cation might be strongly limited and surface waters consequently acidified.  相似文献   

15.
Sr, Nd and Pb isotopic compositions of the Cenozoic basalts were analyzed from Baengnyeongdo Island, Jeongok, Ganseong, and Jejudo Island of Korea. They reveal relatively enriched Sr and Nd isotopic compositions (87Sr/86Sr = 0.703300.70555, 143Nd/144Nd = 0.512980.51256) compared with MORB.207Pb/204Pb and 208Pb/204Pb values of all the analyzed Korean basalts lie above the Northern Hemisphere Reference Line (NHRL) defined by Hart (1984). Pb isotopic compositions of basalts from Jejudo Islands (206Pb/204Pb = 18.6119.12, 207Pb/204Pb = 15.5415.69, 208Pb/204Pb = 38.9839.72) are significantly more radiogenic than the rest (206Pb/204Pb = 17.7218.03, 207Pb/204Pb = 15.4415.58, 208Pb/204Pb = 37.7738.64). The Cenozoic Korean basalts thus can be divided into two groups based on their Sr, Nd and Pb isotopic compositions. The north group reveals mixing between DMM and EM1 while the south group displays DMM-EM2 mixing. Such a distribution is the same as Chinese Cenozoic basalts and it can be interpreted that the subcontinental lithospheric mantle under Korea represents simple lateral continuation of the South and North China Blocks. We suggest that Korean continental collision zone cross the Korean Peninsula through the region between the north and south basalt groups of Korea.  相似文献   

16.
Extensive magmatic activity developed at the northwestern part of the Anatolian block and produced basaltic lavas that are situated along and between the two segments of the North Anatolian Fault zone. This region is a composite tectonic unit formed by collision of continental fragments after consumption of Neotethyan ocean floor during the late Cretaceous. Northwestern Anatolian basalts and evolved lavas exhibit both tholeiitic and calc-alkaline characteristics. Mafic lavas are moderately enriched in LILE (except depleted part of Yuvacık and İznik samples) and depleted in HFSE (but not Zr, Hf) relative to primitive mantle values, suggesting derivation from a MORB-like mantle source that is unexpected in this subduction environment. Sr and Nd isotopes are close to the mantle array and vary beyond analytical error (87Sr/86Sr 0.70404–0.70546, 143Nd/144Nd 0.51270–0.51289). These geochemical features may result from two possible processes: (1) melting of a MORB-like mantle source that was modified by subduction-released fluids and melts or (2) modification of mafic liquids derived from a dominantly MORB-like source by crustal or lithospheric mantle material. Geochemical characteristics of the lavas (e.g., Ba/Rb, Rb/Sr, Ba/Zr, 87Sr/86Sr, Sr/P) vary systematically along the fault zone from east to west, consistent with a decrease in the degree of melting from east to west or a change in the nature of the source composition itself. Thus, the difference in incompatible elements and Sr–Nd isotopic ratios seems to result from small-scale mantle heterogeneity in a post-collisional tectonic environment.  相似文献   

17.
热带地区火山岛/岛弧的化学风化对全球碳循环和海水的Sr同位素演化均有着重要的作用。文章对中国热带海南岛的玄武岩、花岗岩小流域和大河流域进行了河水、地下水、雨水以及基岩和沉积物的综合研究,分析了水样和固体样品的元素含量和Sr同位素比值。结果显示,河床沉积物的化学蚀变指数（CIA）与87Sr/86Sr之间存在着一定的变化关系,而这主要归因于沉积物的阶段性差异风化：风化早期阶段以黑云母占主导,87Sr/86Sr较高。此后斜长石开始风化,87Sr/86Sr逐渐下降。在风化程度中等阶段,斜长石大量分解后,各种富钾矿物风化加剧,87Sr/86Sr值升至最高点。在高风化程度阶段,随着富钾矿物逐渐减少,稳定的风化残余物质占据主导,87Sr/86Sr值逐渐下降。与年轻的活火山岛——加勒比海小安的列斯群岛和印度洋的留尼汪岛相比（其地下化学风化速率2~5倍于地表风化速率）,由于相对较低的降水量和老死火山低的孔隙度,海南岛地下水的流量和固溶物总量（TDS）要低的多,导致海南岛的地下化学风化速率低于地表风化速率,仅与高纬的俄罗斯堪察加活火山岛相近,为小安的列斯群岛和留尼汪岛的约6%~25%,属于全球地下风化贡献最低的区域之一。海南岛玄武岩区的地表化学风化和CO2消耗速率高于法国中央高原和西伯利亚,略低于夏威夷和德干,而显著小于东南亚的爪哇岛和 吕宋岛。在温度相近的条件下,径流量对化学风化速率有着非常明显的控制作用。由于较低的年径流量,热带区域的海南岛,其对大气CO2的消耗能力只是处于一个全球平均的范围内。  相似文献   

18.
Neogene volcanism in the Eastern Rif (Morocco) comprises a series of calc-alkaline, potassic calc-alkaline, shoshonitic and alkaline volcanic rocks. According to new stratigraphical, along with new and previous chronological and geochemical data, the orogenic volcanism was successively (1) calc-alkaline (basaltic andesites and andesites: 13.1 to 12.5 Ma, rhyolites: 9.8 Ma), (2) K-calc-alkaline (basaltic andesitic to rhyolitic lavas and granodiorites: 9.0 to 6.6 Ma), and (3) shoshonitic (absarokites, shoshonites, latites, trachytes: 7.0 to 5.4 Ma). The later Pliocene volcanism was basaltic and alkaline (5.6 to 1.5 Ma). The calc-alkaline and K-calc-alkaline series exhibit lower K2O (0.7–5.3 wt.%), Nb (8–19 ppm) contents and higher 87Sr/86Sr (0.70773–0.71016) than the shoshonitic series (K2O: 2.4–7.2 wt.%, Nb: 21–38 ppm, 87Sr/86Sr: 0.70404–0.70778). Pliocene alkaline basalts have a sodic tendency (Na2O/K2O: 1.7–3.5), high Nb content (up to 52 ppm), and low 87Sr/86Sr ratio (0.70360–0.70413). The variations through time of K2O, Nb and Sr isotopic ratio reflect different mantle sources: (i) calc-alkaline, potassic calc-alkaline and shoshonitic series are derived from a mantle source modified by older subduction, (ii) alkaline basalts are derived mainly from an enriched mantle source. Through time, incompatible elements such as Nb increased while 87Sr/86Sr decreased, suggesting a decreasing influence of metasomatized mantle (inherited subduction). Such evolution is related to the post-collision regimes operating in this area, and could be linked to the succession of extensional, compressional and strike-slip fault tectonics.  相似文献   

19.
David R. Nelson 《Lithos》1989,22(4):265-274
Kimberlites which intruded the Sisimiut (formerly Holsteinsborg) region of central west Greenland during the Early Palaeozoic have initial 87Sr/86Sr between 0.7028 and 0.7033 and εNd between + 1.3 and + 3.9. Mid-Proterozoic potassic lamproites from the same region have initial 87Sr/86Sr between 0.7045 and 0.7060, εNd between −13 and −10 and unradiogenic initial Pb isotopic compositions. The isotopic data favour an asthenospheric mantle source for the kimberlite magmas, in common with “basaltic” kimberlites from other localities, whereas the lamproite magma sources evolved in isolation from the convecting mantle for > 1000 Ma, probably within the subcontinental lithospheric mantle of the Greenland craton, prior to emplacement of the lamproites.  相似文献   

20.
新型杂卤石钾盐矿是近年来发现于四川盆地东北部早—中三叠世的一种可溶性海相固体钾盐,因其可利用性及低成本可开采特征,及其对海相找钾实现突破性进展提供的指示意义,引起了工业界及学术界的广泛关注.但当前以新型杂卤石钾盐矿为载体的海相成钾理论研究尚处于探索阶段,本文聚焦川东北普光地区中下三叠统新型杂卤石钾盐矿,将锶、硫同位素研...  相似文献   

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