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1.
The Sr and Pb isotopes from the 31.6 ± 0.3 Ma (2σ) old Diente del Bufa alkali syenite, northeastern Mexico, and marbles of its contact aureole were used to trace the sources and the mobility of these metals during hydrothermal activity. Chert layers form aquifers within the marbles. The marbles represent aquitards. During fluid-wallrock reaction, the chert layers developed wollastonite rims. Early wollastonite rims have Sr and Pb isotopic compositions similar to those of their immediate host marbles, which indicates that the isotopic composition of Sr and Pb is initially buffered by the marble. Later wollastonite and other replacement minerals rimming the aquifer have Sr and Pb isotopic compositions that carry with time increasingly larger contributions from the high-salinity magmatic brine. The Sr and Pb contributions from the alkali syenite can be traced isotopically for more than 90 m away from the contact of the intrusion. In contrast, Sr and Pb originating from the alkali syenite are traceable within the marbles only for 3 to 5 cm from the aquifer-marble boundary. This distance is comparable to the spatial distribution of isotopic alterations of C and O implying that Sr and Pb were transported into the marbles through a fluid phase. The isotopic variation of Sr, Pb, C, and O across the aquifer-marble profiles reflects infiltration as a transport mechanism rather than diffusion. Because Sr and Pb are minor components in both the infiltrating fluid and the rock and because their concentrations are strongly affected by the distribution coefficients among the solid phases present, there is little correlation between the isotopic compositions of the trace elements Sr and Pb and those of C and O, which are major components in fluid and rock. Very thin meta-argillite rinds at the outer margin of the aquifer represent residual material after the dissolution of calcite. They are distinctly enriched in Rb, Sr, and U. The Rb and Sr are to some extent residual from the original limestone mineralogy, whereas U is dominantly derived from the magmatic fluid and leaked from the aquifer with the escaping immiscible CO2-rich H2O-CO2 fluid that was produced by decarbonation. The 238U/204Pb values ranging from 100 to 250 and distinctly lowered Th/U in the meta-argillite rims (1) demonstrate that U was transported with the magmatic fluid along the aquifer and (2) imply that during unmixing of the highly saline magmatic fluid U fractionated into the CO2-rich H2O-CO2 fluid from which it precipitated selectively in the meta-argillite band across the aquifer. Radioautographs demonstrate that the upper meta-argillite rim has 20 to 40 times more U than the lower rim, which implies that 20 to 40 times more CO2-rich H2O-CO2 fluid has left through the upper aquifer contact. Received: 30 September 1997 / Accepted: 15 December 1997  相似文献   

2.
Pb, Sr and Nd isotopic compositions have been analyzed in recent granites from Northern Africa, Northern Italy and Greece. Lead isotope compositions of K-feldspars are rather homogeneous, and cluster close to the modern lead of Stacey and Kramers (1975) but with slightly higher207Pb/204Pb and208Pb/204Pb ratios. The Cyclades samples, however, have higher206Pb/204Pb ratios. Addition of mantle-derived lead was probably very limited, which supports a quasi-closed system evolution of this element in the continental crust. The Sr, Nd data fall in the enriched part of the143Nd/144Nd vs.87Sr/86Sr diagram and define a smooth hyperbolic mixing curve. Over a wide area, straddling different orogens, most granites may be accounted for by a binary mixture between a recycled crustal component and a depleted mantle-like component. No correlation is observed between either Pb and Sr or Nd isotopic ratios, or any isotopic ratio and major element contents. Quantitative modelling suggests that two cases fit the Sr and Nd characteristics of these granites: they both require anatexis of the crust on a scale large enough to average the isotopic properties of heterogeneous terranes. In the first case, the mantle-derived component may be represented by differentiated Island Arc-type magmas, and the granites result from mixing these magmas with anatectic melts. In the second case, mantle-derived igneous rocks, such as obducted ophiolites, are part of the crustal source and their variable involvement in the anatectic process causes isotopic variations.CRPG Contribution n 630.  相似文献   

3.
Impure limestones with interstratified metachert layers were contact metamorphosed and metasomatized by the Bufa del Diente alkali syenite. Massive marbles exhibit mineralogical and stable isotope evidence for limited fluid infiltration, confined to a 17 m wide zone at the contact. Influx of magmatic brines along most metacherts produced up to 4 cm thick wollastonite rims, according to calcite (Cc)+quartz (Qz)= wollastonite (Wo)+CO2, and were observed at distances of up to 400 m from the contact. The produced CO2 exsolved as an immiscible low density CO2-rich fluid. Chert protolith isotope compositions were 18O (Qz)=27–30%. and 18O (Cc)=24–27%.. Many wollastonites in infiltrated metacherts have low 18O ranging from 11–17 and confirm that decarbonation occurred in presence of a magmatic-signatured fluid. Large gradients in 18O (Wo) across the rims may reach 6 The 18O of remaining quartz is often lowered to 15–20 whereas caleites largely retained their original compositions. The isotopic reversals of up to 10 between quartz and calcite along with reaction textures demonstrate non-equilibrium between infiltrating fluid in the aquifer and the assemblage calcite+quartz+wollastonite. This is compatible with the assumption of a down-temperature flow of magmatic fluids that occurred exclusively in the remaining quarzite layer. The 13C (Cc) and 18O (Cc) of marble calcites measured perpendicular to two metachert bands reveal significant isotopic alterations along distances of 4.5 cm and 7.5 cm from the wollastonite-marble boundary only into the hanging wall marble, suggesting an advection process caused by a fluid phase which movel upwards. Covariation trends of 13C (Cc) and 18O (Cc) across the alteration front indicate that this fluid was CO2-rich. Mass balance calculations show that all CO2-rich fluid produced by the decarbonation reaction was lost into overlying marble. The metachert aquifers did not leak with respect to water-rich fluids.  相似文献   

4.
Neodymium, Sr and Pb isotopic compositions, along with rare earth element (REE) concentrations were determined for twelve black ores and one yellow ore from twelve localities of the Kuroko deposits, Japan. The ores were generated by submarine hydrothermal activity during the Miocene age. Neodymium isotopic compositions of the ores (Nd: –4.9 to +6.5) mostly overlap with spatially associated igneous rocks. On a Nd versus Sr isotopic correlation diagram, however, 87Sr/86Sr ratios are shifted from the associated igneous rocks towards the higher contemporaneous seawater ratio. REE patterns are highly variable, ranging from light REE enriched to depleted, and show no Ce anomalies, as would be expected if they were derived from seawater. These results suggest that the REEs contained in ores were mainly derived from the associated igneous rocks, but that the ore Sr is a mixture derived from both seawater and the igneous rocks. Most Pb isotopic compositions fall within the range defined by the associated igneous rocks (206Pb/204Pb=18.35–18.84, 207Pb/204Pb=15.59–15.97 and 208Pb/204Pb=38.53–39.90), although several samples have very radiogenic compositions that were most likely derived from basement rocks. Our new Pb isotopic results display greater variation, and have a larger range of more radiogenic compositions than has been noted previously for these ores. In addition, the black ore with the most radiogenic Pb isotopic composition also has the least radiogenic Nd isotopic composition. This suggests that at least some of the Pb contained in the ores was derived mainly from older basement rocks. The large positive Eu anomalies for some black ores are consistent with a high-temperature origin for the parental fluids, irrespective of the source rock. The single yellow ore examined, however, has a small negative Eu anomaly, which may indicate derivation from a lower temperature fluid. Previous studies suggested that the Kuroko ores were formed in the presence of organic materials in an anoxic basin. Combined Nd, Sr, Pb and Os isotopic and REE abundance data indicate that multiple sources were involved in the genesis of Kuroko ores.  相似文献   

5.
《Applied Geochemistry》1997,12(5):607-623
The aim of this study is to characterize the processes and phases which control migration and retention of rare earth elements (REE) in a heavy metal contaminated soil. In addition to concentration data, we used Pb, Sr and Nd isotopic compositions in order to distinguish between natural and anthropogenic trace metals and to characterize the phases leached away during the sequential extraction procedure.The samples were sequentially extracted in 3 steps with 1 N acetic acid (HAc), 1 N HCl and 1 N HNO3. The Pb isotope data showed that anthropogenic Pb had mainly been retained in the uppermost 10 cm by the organic matter of the topsoil. The87Sr/86Sr ratios of the HAc extracts are almost constant and indicate that soil carbonate is derived from regionally outcropping carbonate-rich sediments. Most HCl and HNO3 extracts have more radiogenic Sr isotopic compositions, but it is unclear whether this reflects a growing influence of anthropogenic or silicate-derived Sr.The depth distribution of the REE is mainly controlled by two different parameters: soil pH for the HAc extractable REE and FeMn oxides for the REE in the HCl and HNO3 extracts. A part of the HNO3 extractable REE was also bound to the organic matter of the topsoil. The REE concentrations in the HAc extractable phase increase with depth and increasing soil pH, which indicates that they are derived from the surface and hence are of anthropogenic origin. This is confirmed by143Nd/144Nd isotope ratios which show a mixing between a natural end-member at the top and an anthropogenic end-member at the base of the profile. We assume that the anthropogenic REE were transported in dissolved form as carbonate complexes and then precipitated during downward migration as soil pH increased.  相似文献   

6.
The Valentine wollastonite skarn in the north-west Adirondack Mountains, New York, is a seven million ton deposit which resulted from channellized infiltration of H2O-rich, silica-bearing fluids. The wollastonite formed by reaction of these fluids with non-siliceous calcite marble. The skarn formed at the contact of the syenitic Diana Complex and was subsequently overprinted by Grenville-age granulite facies metamorphism and retrograde hydrothermal alteration during uplift. Calcite marbles adjacent to the deposit have generally high δ18O values (c. 21‰), typical of Grenville marbles which have not exchanged extensively with externally derived fluids. Carbon isotopic fractiona-tions between coexisting calcite and graphite in the marbles indicate equilibration at 675d? C, consistent with the conditions of regional metamorphism. Oxygen isotopic ratios from wollastonite skarn are lower than in the marbles and show a 14‰ variation (-1‰ to 13‰). Some isotopic heterogeneity is preserved from skarn formation, and some represents localized exchange with low-δ18O retrograde fluids. Detailed millimetre- to centimetre-scale isotopic profiles taken across skarn/marble contacts reveal steep δ18O gradients in the skarn, with values increasing towards the marble. The gradients reflect isotopic evolution of the fluid as it reacted with high δ18O calcite to form wollastonite. Calcite in the marble preserves high δ18O values to within <5 mm of the skarn contact. The preservation of high δ18O values in marbles at skarn contacts and the disequilibrium fractionation between wollastonite skarn and calcite marble across these contacts indicate that the marbles were not infiltrated with significant quantities of the fluid. Thus, the marbles were relatively impermeable during both the skarn formation and retrograde alteration. Skarn formation may have been episodic and fluid flow was either chaotic or dominantly parallel to lithological contacts. Although these steep isotope gradients resemble fluid infiltration fronts, they actually represent the sides of the major flow system. Because chromatographic infiltration models of mass transport require the assumption of pervasive fluid flow through a permeable rock, such models are not applicable to this hydrothermal system and, by extension, to many other metamorphic systems where low-permeability rocks restrict fluid migration pathways. Minimum time-integrated fluid fluxes have been calculated at the Valentine deposit using oxygen isotopic mass balance, reaction progress of fluid buffering reactions, and silica mass balance. All three approaches show that large volumes of fluid were necessary to produce the skarn, but silica mass balance calculations yield the largest minimum flux and are hence the most realistic.  相似文献   

7.
Omai is a high tonnage, low-grade, world-class gold deposit located in the Paleoproterozoic Guiana Shield. It is the second most important gold deposit in the Guiana Shield (after Las Cristinas, Venezuela), and one of the largest in South America (4.0 million oz.). Sm-Nd and Sr isotope data are presented for host rocks and for scheelite from auriferous quartz-carbonate-scheelite-sulfide-telluride veins from the Omai deposit. Gold-bearing veins are hosted by the Paleoproterozoic Barama-Mazaruni Supergroup, a greenstone belt sequence consisting of mafic volcanic rocks interbedded with sedimentary rocks that are intruded by quartz-feldspar porphyry and rhyolite dikes. This lithologic sequence was folded and metamorphosed to lower greenschist facies during the Paleoproterozoic Trans-Amazonian orogeny. The volcano-sedimentary unit was intruded by a post-tectonic quartz monzodiorite-diorite-hornblendite stock. Initial Nd isotope ratios for the Omai volcanic rocks range from ɛNd=+2.1 to +4.2. These values suggest that this part of the Guiana Shield was a site of new crust formation during the Paleoproterozoic and was not contaminated by older (Archean), reworked continental crust. Initial Nd isotope ratios for the Omai stock range between +0.5 and +2.3, which suggest limited contamination with previously formed continental crust. Although the Nd isotopic ratios of gold-related scheelites overlap with those of the host rocks, particularly the tholeiitic basalts at the interpreted time of vein emplacement, the lack of both isotopic mixing and significant Nd movement during the hydrothermal process suggest that the Nd isotope composition can be used to determine the isotopic characteristics of the ore fluid source area. At Omai, the ore fluid is largely derived from a radiogenic Nd source, represented by mantle or lower crustal reservoirs. Strontium isotope ratios for the scheelites cluster tightly between 0.7019 and 0.7021. The Sr isotope data suggest that unlike Nd, Sr was significantly mobile during the hydrothermal process. The fluids responsible for the Omai deposit may have picked up Sr along the flow path. The constant low Sr isotope values of scheelites probably reflect the key role that the local tholeiitic basalts played as the main source of Sr in the fluids. Whereas Nd isotopes identify the fluid source area, the Sr isotopes map the fluid flow paths. Received: 11 February 1999 / Accepted: 1 November 1999  相似文献   

8.
SIMONETTI  A.; BELL  K. 《Journal of Petrology》1994,35(6):1597-1621
Initial Nd, Pb, and Sr isotopic data from carbonatites and associatedintrusive silica-undersaturated rocks from the early Jurassic,Chilwa Island complex, located in southern Malawi, central Africa,suggest melt derivation from a Rb/Sr- and Nd/Sm-depleted butTh/Pb- and U/Pb-enriched mantle source. Initial 143Nd/144Nd(0.51265–0.51270) isotope ratios from the Chilwa Islandcarbonatites are relatively constant, but their initial 87Sr/86Sr(0.70319–0.70361) ratios are variable. The 18Osmow (9.53–14.15%0)and 13CPDB (–3.27 to –1.50%0) isotope ratios ofthe carbonates are enriched relative to the range of mantlevalues, and there is a negative correlation between 18O andSr isotope ratios. The variations in Sr, C, and O isotopic ratiosfrom the carbonatites suggest secondary processes, such as interactionwith meteoric groundwater during late-stage carbonatite activity.The initial 143Nd/144Nd (0.51246 0.51269) and initial 87Sr/86Sr(0.70344–0.70383) isotope ratios from the intrusive silicaterocks are more variable, and the Sr more radiogenic than thosefrom the carbonatites. Most of the Pb isotope data from Chilwa Island plot to the rightof the geochron and close to the oceanic regression line definedby MORBs and OIBs. Initial Pb isotopic ratios from both carbonatites(207Pb/204Pb 15.63–15.71; 206Pb/204Pb 19.13–19.78)and silicate rocks (207Pb/204Pb 15.61–15.72; 206Pb/204Pb18.18–20.12) show pronounced variations, and form twogroups in Pb-Pb plots. The isotopic variations shown by Nd, Pb, and Sr for the ChilwaIsland carbonatites and intrusive silicates suggest that thesemelts underwent different evolutionary histories. The chemicaldata, including isotopic ratios, from the carbonatites and olivinenephelinites are consistent with magmatic differentiation ofa carbonated-nephelinite magma. A model is proposed in whichdifferentiation of the carbonatite magma was accompanied byfenitization (metasomatic alteration) of the country rocks bycarbonatite-derived fluids, and subsequent alteration of thecarbonatite by hydrothermal activity. The chemical and isotopicdata from the non-nephelinitic intrusive silicate rocks reveala more complex evolutionary history, involving either selectivebinary mixing of lower-crustal granulites and a nephelinitemagma, or incremental batch melting of a depleted source andsubsequent crustal contamination.  相似文献   

9.
Associated with the Cretaceous Okorusu carbonatite complex (Namibia) is a hydrothermal fluorite mineralization hosted in Pan-African country rock marbles, which resulted from fluid-rock reaction between the marbles and orthomagmatic, carbonatitic fluids expelled from the carbonatite. Yellow fluorite I was deposited in veins up to 5 cm away from the wallrock contact, followed by purple and colorless fluorite II, smoky quartz and barite, a Mn-rich crust on early calcite, and pure calcite. This clear-cut sequence of mineral growth allows an investigation into fluid-rock interaction processes between the marble and the migrating carbonatitic fluid, and element fractionation patterns between the fluid and subsequent hydrothermal precipitates.Fluorite I shows a progressive change in color from dark yellow to colorless with purple laminations over time of deposition. Subsequent fluorite I precipitates show an increase in Ca, and a continuous decrease in F, Sr, REE, Y, Th, U and Pb contents. The ratios (Eu/Eu*)cn, Th/Pb and U/Pb increase whereas Y/Ho, Th/U and (La/Yb)cn decrease. The Sr-isotopic composition remains constant at 87Sr/86Sr = 0.70456-0.70459, but with varying, highly radiogenic Pb (206Pb/204Pb = 32-190, 238U/204Pb = 7-63). Fluorite II has 87Sr/86Sr = 0.70454-0.70459, 206Pb/204Pb = 18.349, and 207Pb/204Pb = 15.600, and a chemical composition similar to youngest fluorite I. The Mn-rich crust on early calcite accumulated REE, Ba, Pb, Zr, Cs, Th and U, developing into pure calcite with a prominent negative Ce anomaly and successively more radiogenic Sr. The calculated degrees of fluid-rock interaction, f = weight fraction of fluid/(fluid + marble), decrease from fluorite I and most fluorite II (f = 0.5) to calcite (f = 0.2-0.3) and hydrothermal quartz (f ? 0.1). A crush-leach experiment for fluid inclusions in the hydrothermal quartz yielded a Rb-Sr isochron age of 103 ± 12 Ma. Crush-leach analysis for the carbonatitic fluid trapped in the wallrock yielded a trend from the fluid leachate to the host quartz (206Pb/204Pb = 18.224 and 18.602, 207Pb/204Pb = 15.616 and 15.636, respectively) extending from carbonatite towards crustal rocks.Calculated trace element distribution coefficients fluorite/fluid are below unity throughout, and increase from La to Yb. Elements largely excluded from fluorite (Ba, Pb, LREE relative to HREE) were incorporated later into the Mn-rich crust on calcite. The trace element patterns of the hydrothermal minerals are related to changing aCO2 and aF− in the fluid during continued fluid-marble reaction. A predominance of carbonate over fluoride complexing in the fluid as reactions proceeded controlled the Y/Ho, Th/U and REE patterns in the fluid and the crystallizing phases. Deviations from these trends indicate discontinuous processes of fluid-rock reaction.  相似文献   

10.
The high-grade metamorphic basement of the Modum Complex, South Norway,exhibits retrogradation and alteration due to late stage fluid infiltration.Extensive alteration zones of albite-and calcite-rich veining occur especiallywithin and around numerous metagabbros. The gabbros, intruded at 1224±15Ma, are now partly altered to amphibolites due to the subsequent high-grade metamorphism.Two generations of albite-rich rocks have been recognized: (1) a fine-grained, foliated type;(2) a coarse-grained, crosscutting type. Both types show a typical greenschist facies mineralassemblage; albite ± actinolite ± chlorite ± talc. The calcite veins/dykesrepresent a younger generation of veins than both albite-rich types. U–Pb data for spheneof type (1) yielded an age of 1080±3 Ma, determining a point on the retrogradeP-T-t path of the Modum Complex. Increasing albitisation of themetagabbros leads to a decrease in(143ND/144Nd)oand an increase in (87Sr/86)o.Albite- and calcite-rich samples show negative Nd and positive Sr, suggesting that fluids which interacted with the metagabbros originated from a crustal reservoir. The Nd and Sr isotopic data show disequilibrium at the microscale as well as at the macroscale. Negative Sm–Nd model ages of the albite-rich rocks demonstrate that rare-earth elements (REEs) were mobile and fractionated during albitisation.  相似文献   

11.
The occurrence of a charnockitised felsic gneiss adjacent to a marble/calc-silicate horizon at Nuliyam, southern India, has been cited in recent literature as a classic example of the dehydration of crustal rocks resulting from the advective infiltration of CO2-rich fluids generated from a local carbonate source. Petrographic study of the Nuliyam calc-silicate, however, reveals it to consist of abundant wollastonite and scapolite and contain locally discordant veins rich in wollastonite. At the pressure—temperature conditions proposed for charnockite formation in recent studies, 5 kbar and 725°C, this wollastonite-bearing mineral assemblage was stable in the presence of a fluid phase only if X CO2 was near 0.25 and could not have coexisted with the fluid causing biotite breakdown and charnockite development in adjacent rocks (X CO2>0.85). The stable coexistence of wollastonite and scapolite prohibits the calc-silicate from being a source for fluid driving charnockitisation at the required P-T conditions. Textural observations such as the limited replacement of wollastonite by calcite+quartz symplectites and mosaics, are consistent with late fluid infiltration into the calc-silicate. The extensive isotopic, chemical and mineral abundance data of Jackson and Santosh (1992) are re-interpreted and integrated with these observations to develop a model involving the infiltration of an externally derived CO2-rich fluid during high-temperature decompression. Increased charnockite development next to the calc-silicate has arisen because the calc-silicate acted as a relatively unreactive and impermeable barrier to fluid transport and caused fluid ponding beneath antiformal closures. The Nuliyam charnockite/calc-silicate locality is an example of a structural trap in a metamorphic setting rather than a site where charnockite formation can be attributed to local fluid sources.  相似文献   

12.
Strong compositional zonation of the 34 Ma Grizzly Peak Tuff in west-central Colorado is attended by non-monotonic trends in O, Sr, Nd, and Pb isotope ratios. Fiamme from the tuff cluster in chemical compositions and petrographic characteristics, indicating the magma chamber was not continuously zoned but consisted of at least seven compositional layers. The most mafic magma erupted (57 wt% SiO2, fiamme group 7) had 18O= +8.5, initial 87Sr/86Sr=0.7099, Nd, and 206Pb/204Pb=17.80, suggesting that the magma was produced by 50% fractional crystallization of basaltic magma that assimilated 20 to 40 wt% Proterozoic crust. Isotopic compositions of more evolved parts of the chamber (up to 77 wt% SiO2, fiamme group 1) depart from the mafic base-level composition of fiamme group 7, and reflect late-stage assimilation that occurred largely after compositional layering was established. 18O values decrease by as much as 1.5 from fiamme groups 7 through 4, indicating assimilation of hydrothermally altered roof rocks. 18O values abruptly inerease by up to 1.5 between fiamme groups 4 and 3. This discontinuity is interpreted to reflect evolution in an asymmetric chamber that had a split-level roof, allowing assimilation of wall rocks that varied vertically in degree of hydrothermal alteration. This chamber geometry is also supported by collapse structures in the caldera. Late-stage assimilation of heterogeneous wall rocks is also indicated by variations in Sr, Nd, and Pb isotope ratios. Large Sr isotope disequilibrium exists between some phenocrysts and whole-rock fiamme, and initial 87Sr/86Sr ratios in phenocrysts are as high as 0.7170. values regularly increase from-13.0 in fiamme group 7 to-11.3 in fiamme group 3, and then decrease to-12.2 in fiamme group 1. 206Pb/204Pb ratios generally increase from 17.80 to 17.94 for fiamme groups 7 through 1. The rhyolitic parts of the Grizzly Peak Tuff have isotopic compositions that could be attributed to a purely crustal melt. It is unlikely, however, that the mafic parts of the tuff were generated by crustal melting, and the compositional and isotopic variations across the entire zonation of the tuff are best explained by fractional crystallization of mantle-derived magmas, accompanied by extensive assimilation of Proterozoic crust.  相似文献   

13.
A detailed isotopic study of minerals and whole rocks from the Cretaceous Oka complex, Quebec, Canada, shows a very small variation in initial Nd and Sr isotopic compositions. Assuming an age of 109 Ma for the complex, apatite, calcite, garnet, melilite, monticellite, olivine and pyroxene and whole rocks yield a range for initial 87Sr/86Sr of 0.70323–0.70333; and for initial 143Nd/144Nd of 0.51271–0.51284 ( SR(T)= –14.8 to –16.2; Nd(T)=+4.1 to +6.6). The negative SR and positive Nd indicate derivation of the Nd and Sr from a source with a time-integrated depletion in the large-ion lithophile (LIL) elements. This agrees with data from other Canadian carbonatites and confirms that a large part of the Canadian Shield is underlain by a source region depleted in the LIL elements. The new data from Oka suggest that the depleted source may have remained coupled to the continental crust until recent time.  相似文献   

14.
Pb, Sr and Nd isotope variations are correlated in diverse lavas erupted at small seamounts near the East Pacific Rise. Tholeiites are isotopically indistinguishable from MORB (206Pb/204Pb=18.1–18.5; 87Sr/86Sr=0.7023–0.7028; 143Nd/144Nd=0.51326-0.51308); associated alkali basalts always show more radiogenic Pb and Sr signatures (206Pb/204Pb=18.8–19.2; 87Sr/86Sr=0.7029–0.7031) and less radiogenic Nd (143Nd/144Nd=0.51289–0.51301). The isotopic variability covers 80% of the variability for Pacific MORB, due to the presence of small-scale heterogeneity in the underlying mantle. Isotope compositions also correlate with trace element ratios such as La/Sm. Tholeiites at these seamounts have 3He/4He between 7.8–8.7 R A(R A= atmospheric ratio), also indistinguishable from MORB. He trapped in vesicles of alkali basalts, released by crushing in vacuo, has low 3He/4He (1.2–2.6 R)Ain conjunction with low helium concentrations ([He]<5×10–8 ccSTP/g). In many cases post-eruptive radiogenic ingrowth has produced He isotope disequilibrium between vesicles and glass in the alkali basalts; subatmospheric 3He/4He ratios characterize the He dissolved in the glass which is released by melting the crushed powders. The narrow range of 3He/4He in the vesicles of the alkali basalts suggests that low 3He/4He is a source characteristic, but given their low [He] and high (U + Th), pre-eruptive radiogenic ingrowth cannot be excluded as a cause for low inherited 3He/4He ratios. Pb, Sr and Nd isotope compositions in lavas erupted at Shimada Seamount, an isolated volcano on 20 m.y. old seafloor at 17°N, are distinctly different from other seamounts in the East Pacific (206Pb/204Pb=18.8–19.0, 87Sr/ 86Sr0.7048 and 143Nd/144Nd0.51266). Relatively high 207Pb/204Pb (15.6–15.7) indicates ancient (>2 Ga) isolation of the source from the depleted upper mantle, similar to Dupal components which are more prevalent in the southern hemisphere mantle. 3He/4He at Shimada Seamount is between 3.9–4.8 R A. Because the helium concentrations range up to 1.5×10–6, the low 3He/4He can not be due to radiogenic accumulation of 4He in the magma for reasonable volcanic evolution times. The low 3He/4He may be due to the presence of enriched domains within the lithosphere with high (U + Th)/He ratios, possibly formed during its accretion near the ridge. Alternatively, the low 3He/4He may be an inherent characteristic of an enriched component in the mantle beneath the East Pacific. Collectively, the He-Pb-Sr-Nd isotope systematics at East Pacific seamounts suggest that the range of isotope compositions present in the mantle is more readily sampled by seamount and island volcanism than by axial volcanism. Beneath thicker lithosphere away from the ridge axis, smaller degrees of melting in the source regions are less efficient in averaging the chemical characteristics of small-scale heterogeneities.  相似文献   

15.
The preservation of premetamorphic, whole-rock oxygen isotope ratios in Adirondack metasediments shows that neither these rocks nor adjacent anorthosites and gneisses have been penetrated by large amounts of externally derived, hot CO2-H2O fluids during granulite facies metamorphism. This conclusion is supported by calculations of the effect of fluid volatilization and exchange and is also independently supported by petrologic and phase equilibria considerations. The data suggest that these rocks were not an open system during metamorphism; that fluid/rock ratios were in many instances between 0.0 and 0.1; that externally derived fluids, as well as fluids derived by metamorphic volatilization, rose along localized channels and were not pervasive; and thus that no single generalization can be applied to metamorphic fluid conditions in the Adirondacks.Analyses of 3 to 4 coexisting minerals from Adirondack marbles show that isotopic equilibrium was attained at the peak of granulite and upper amphibolite facies metamorphism. Thus the isotopic compositions of metamorphic fluids can be inferred from analyses of carbonates and fluid budgets can be constructed.Carbonates from the granulite facies are on average, isotopically similar to those from lower grade or unmetamorphosed limestones of the same age showing that no large isotopic shifts accompanied high grade metamorphism. Equilibrium calculations indicate that small decreases in 18O, averaging 1 permil, result from volatilization reactions for Adirondack rock compositions. Additional small differences between amphibolite and granulite facies marbles are due to systematic lithologie differences.The range of Adirondack carbonate 18O values (12.3 to 27.2) can be explained by the highly variable isotopic compositions of unmetamorphosed limestones in conjunction with minor 18O and 13C depletions caused by metamorphic volatilization suggesting that many (and possibly most) marbles have closely preserved their premetamorphic isotopic compositions. Such preservation is particularly evident in instances of high 18O calcites (25.0 to 27.2), low 18O wollastonites (–1.3 to 3.5), and sharp gradients in 18O (18 permil/15m between marble and anorthosite, 8 permil/25 m in metasediments, and 6 permil/1 m in skarn).Isotopic exchange is seen across marble-anorthosite and marble-granite contacts only at the scale of a few meters. Small (<5 m) marble xenoliths are in approximate exchange equilibrium with their hosts, but for larger xenoliths and layers of marble there is no evidence of exchange at distances greater than 10 m from meta-igneous contacts.  相似文献   

16.
Isotopic ratios of Nd and Sr have been measured in a suite of samples spanning most of the exposed stratigraphy of the Skaergaard intrusion in order to detect and quantify input (such as assimilated wallrock and fresh magma) into the magma chamber during crystallization. Unlike 18O and D, Nd and Sr isotope ratios do not appear to have been significantly affected by circulation of meteoric waters in the upper part of the intrusion. Variations in initial 87Sr/86Sr and Nd suggest that the Skaergaard magma chamber was affected during its crystallization by a small amount (2%–4%) of assimilation of Precambrian gneiss wallrock (high 87Sr/86Sr, low Nd) and possibly recharge of uncontaminated magma. Decreases in Nd and increases in 87Sr/86Sr during the early stages (0%–30%) of crystallization give way to approximately unchanging isotopic ratios through crystallization of the latest-deposited cumulates. Modelling of assimilation-fractional crystallization-recharge processes using these data as constraints shows that the assimilation rate must have been decreasing throughout crystallization. In addition, the isotope data allow replenishment by an amount of uncontaminated magma equal to 20%–30% of the total intrusion mass, occurring either continuously or in pulses over the first 75% of crystallization. Comparison of the recharge models with published Mg/(Mg+Fe2+) data from Skaergaard cumulates shows that the modelled replenishment rates are not inconsistent with available major element data, although significant recharge during the final 25% of crystallization can be ruled out. The isotope data show that the Skaergaard magma could have incorporated only a small amount of the gneiss that it displaced from the floor of the chamber; assimilation appears to have taken place primarily across a partially molten zone that formed at the roof from the wallrock that was dislodged during emplacement. In the latest stages of crystallization (>75% crystallized), the Skaergaard magma may have become stratified into two separately-convecting layers, effectively insulating Layered Series cumulates from further contamination.  相似文献   

17.
Seven hundred and twenty-five Sr, two hundred and forty-three Nd and one hundred and fifty-one Pb isotopic ratios from seven different Mexican magmatic provinces were compiled in an extensive geochemical database. Data were arranged according to the Mexican geological provinces, indicating for each province total number of analyses, range and mean of values and two times standard deviation (2σ). Data from seven provinces were included in the database: Mexican Volcanic Belt (MVB), Sierra Madre Occidental (SMO), Baja California (BC), Pacific Ocean (PacOc), Altiplano (AP), Sierra Madre del Sur (SMS), and Sierra Madre Oriental (SMOr). Isotopic values from upper mantle and lower crustal xenoliths, basement outcrops and sediments from the Cocos Plate were also compiled. In the MVB the isotopic ratios range as follows:87Sr/86Sr 0.703003-0.70841;143Nd/144Nd 0.512496-0.513098;206Pb/204Pb 18.567-19.580;207Pb/204Pb 15.466-15.647;208Pb/204Pb 38.065-38.632. The SMO shows a large variation in87Sr/86Sr ranging from ∼0.7033 to 0.71387.143Nd/144Nd ratios are relatively less variable with values from 0.51191 to 0.51286. Pb isotope ratios in the SMO are as follows:206Pb/204Pb 18.060-18.860;207Pb/204Pb 15.558-15.636;208Pb/204Pb 37.945-38.625. PacOc rocks show the most depleted Sr and Nd isotopic ratios (0.70232-0.70567 for Sr and 0.512631-0.513261 for Nd). Pb isotopes for PacOc show the following range:206Pb/204Pb 18.049-19.910;207Pb/2047Pb 15.425-15.734;208Pb/204Pb 37.449-39.404. The isotopic ratios of the AP rocks seem to be within the range of those from the PacOc. Most samples with reported Sr and Nd isotopic data are spread within and around the “mantle array”. The SMO seems to have been formed by a mixing process between mantle derived magmas and continental crust. The MVB appears to have a larger mantle component, with AFC as the dominant petrogenetic process for the evolved rocks. There is still a need for Pb isotopic data in all Mexican magmatic provinces and of Nd isotopes in BC, AP, SMS, and SMOr.  相似文献   

18.
Alkalic and tholeiitic basalts were erupted in the central Arizona Transition Zone during Miocene-Pliocene time before and after regional faulting. The alkalic lava types differ from the subalkaline lavas in Sr, Nd and Pb isotopic ratios and trace element ratios and, despite close temporal and spatial relationships, the two types appear to be from discrete mantle sources. Pre-faulting lava types include: potassic trachybasalts (87Sr/86Sr = 0.7052 to 0.7055, Nd= –9.2 to –10.7); alkali olivine basalts (87Sr/ 86Sr = 0.7049 to 0.7054, Nd= –2 to 0.2); basanite and hawaiites (87Sr/86Sr = 0.7049 to 0.7053, Nd= –3.5 to –7.8); and quartz tholeiites (87Sr/86Sr = 0.7047, Nd= –1.4 to –2.6). Post-faulting lavas have lower 87Sr/86Sr (<0.7045) and Nd from –3.2 to 2.3. Pb isotopic data for both preand post-faulting lavas form coherent clusters by magma type with values higher than those associated with MORB but within the range of values found for crustal rocks and sulfide ores in Arizona and New Mexico. Pb isotopic systematics appear to be dominated by crustal contamination. Effects of assimilation and fractional crystallization are inadequate to produce the Sr isotopic variations unless very large amounts of assimilation occurred relative to fractionation. It is impossible to produce the Nd isotopic variations unless ancient very unradiogenic material exists beneath the region. Moreover the assumption that the alkalic lavas are cogenetic requires high degrees of fractionation inconsistent with major- and trace-element data. Metasomatism of the subcontinental lithosphere above a subduction zone by a slab-derived fluid enriched in Sr, Ba, P and K could have produced the isotopic and elemental patterns. The degree of metasomatism apparently decreased upward, with the alkalic lavas sampling more modified regions of the mantle than the tholeiitic lavas. Such metasomatism may have been a regional event associated with crustal formation at about 1.6 Ga. Disruption and weakening of the subcontinental lithosphere in the Transition Zone of the Colorado Plateau by volcanism probably made deformation possible.  相似文献   

19.
Crustal contamination of basalts located in the western United States has been generally under-emphasized, and much of their isotopic variation has been ascribed to multiple and heterogeneous mantle sources. Basalts of the Miocene Columbia River Basalt Group in the Pacific Northwest have passed through crust ranging from Precambrian to Tertiary in age. These flows are voluminous, homogenous, and underwent rapid effusion, all of which are disadvantages for crustal contamination while en route to the surface. The Picture Gorge Basalt of the Columbia River Basalt Group erupted through Paleozoic and Mesozoic oceanic accreted terranes in central Oregon, and earlier studies on these basalts provided no isotopic evidence for crustal contamination. New Sr, Nd, Pb, and O isotopic data presented here indicate that the isotopic variation of the Picture Gorge Basalt is very small, 87Sr/86Sr=0.70307–0.70371, Nd=+7.7-+4.8, 18O=+5.6±6.1, and 206Pb/204Pb=18.80–18.91. Evaluation of the Picture Gorge compositional variation supports a model where two isotopic components contributed to Picture Gorge Basalt genesis. The first component (C1) is reflected by low 87Sr/86Sr, high Nd, and nonradiogenic Pb isotopic compositions. Basalts with C1 isotopic compositions have large MgO, Ni, and Cr contents and mantle-like 18O=+5.6. C1 basalts have enrichments in Ba coupled with depletions in Nb and Ta. These characteristics are best explained by derivation from a depleted mantle source which has undergone a recent enrichment by fluids coming from a subducted slab. This C1 mantle component is prevalent throughout the Pacific Northwest. The second isotopic component has higher 87Sr/ 86Sr and 18O, lower Nd, and more radiogenic Pb isotopic compositions than C1. There is a correlation in the Picture Gorge data of Sr, Nd, and Pb isotopes with differentiation indicators such as decreasing Mg#, and increasing K2O/TiO2, Ba, Ba/Zr, Rb/Sr, La/Sm, and La/Yb. Phase equilibrium and mineralogical constraints indicate that these compositional characteristics were inherited in the Picture Gorge magmas at crustal pressures, and thus the second isotopic component is most likely crustal in origin. Mixing and open-system calculations can produce the isotopic composition of the most evolved Picture Gorge flows from the most primitive compositions by 8 to 21% contamination of isotopic compositions similar to accreted terrane crust found in the Pacific Northwest. Therefore, in spite of the disadvantages for crustal contamination and their narrow range in isotopic compositions, the process controlling isotopic variation within the Picture Gorge Basalt is primarily crustal contamination. We suggest that comprehensive analyses for basaltic suites and careful consideration of these data must be made to test for crustal contamination, before variation resulting from mantle heterogeneity can be assessed.Deceased  相似文献   

20.
Summary The eastern part of the agpaitic Khibina complex is characterized by the occurrence of dykes of various alkali silicate rocks and carbonatites. Of these, picrite, monchiquite, nephelinite and phonolite have been studied here. Whole rock and mineral geochemical data indicate that monchiquites evolved from a picritic primary magma by olivine+ magnetite fractionation and subsequent steps involving magma mixing at crustal levels. None of these processes or assimilation/magma mixing of wall rocks or other plutonic rocks within the complex can entirely explain the geochemical and Nd–Sr-isotopic characteristics of the monchiquites (i.e. a covariant alignment between (87Sr/86Sr)370=0.70367, (143Nd/144Nd)370=0.51237 and (87Sr/86Sr)370=0.70400, (143Nd/144Nd)370=0.51225 representing the end points of the array). This signature points to isotopic heterogeneities of the mantle source of the dyke-producing magma. The four mantle components (i.e. depleted mantle, lower mantle plume component, EMI-like component and EMII-like component) must occur in different proportions on a small scale in order to explain the isotopic variations of the dyke rocks. The EMII-like component might be incorporated into the source area of the primary magma by carbonatitic fluids involving subducted crustal material. The most likely model to explain the small-scale isotopic heterogeneity is plume activity. The results of this study do not provide any support to a cogenetic origin (e.g. fractionation or liquid immiscibility) for carbonatite and monchiquite or other alkali-silicate dyke rocks occurring in spatial proximity. Instead, we propose that both, carbonatite and picrite/monchiquite, originated by low-degree partial melting of peridotite. Textural observations, mineralogical data, and C and O isotopic compositions suggest incorporation of calcite from carbonatite in monchiquite and the occurrence of late-stage carbothermal fluids.Supplementary material to this paper is available in electronic form at http://dx.doi.org/10.1007/s00710-003-0016-2  相似文献   

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