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1.
Whole-rock oxygen isotope compositions of cores and cuttings from Long Valley exploration wells show that the Bishop Tuff has been an important reservoir for both fossil and active geothermal systems within the caldera. The deep Clay Pit-1 and Mammoth-1 wells on the resurgent dome penetrate mildly to strongly altered Bishop Tuff with δ18OWR values as low as −2.6% (vs V-SMOW). The idfu 44-16 well intercepts a thinner Bishop Tuff section with δ18OWR values of +0.4 to +2.3%. in the western caldera moat, where milder and more sporadic 18O depletions occur in Tertiary volcanic rocks of the western caldera floor (δ18OWR = +2.2 to +6.4‰). Bishop Tuff samples from deeper parts of the 715 m rdo-8 (Shady Rest) well in the SW moat are also strongly depleted in 18O (δ18OWR = −1.5 to +0.6‰). Four shallow thermal gradient wells (469–715 m td drilled in the western moat did not penetrate Bishop Tuff, but Early Rhyolites from two of these holes are depleted in 18O (δ18OWR = −1.2 to +6.0‰ inplv-1 +4.6 to +5.3%. inmlgrap-1), compared to lithologic equivalents from the other two holes (δ18OWR = +6.3 to +8.0‰ inplv-2 andmlgrap-2).Whole-rock oxygen isotope profiles for the resurgent dome wells are unlike profiles calculated assuming alkali feldspar-H2O fractionation behavior and total O-isotopic equilibration with −14.3‰ fluids at measured temperatures. The sense of this divergence implies an earlier hydrothermal episode within the central caldera driven by one or more shallow intrusions. Geochemical similarities between an intrusive granophyre at the bottom of the Clay Pit-1 well and a nearby Moat Rhyolite dome with a K/Ar cooling age of 0.5 Ma suggest that vigorous hydrothermal activity beneath the central resurgent dome may have occurred as much as 0.5 m.y. ago. Calculated and measured O-isotope profiles are similar for deep wells that penetrate the western moat of the caldera, where steep temperature gradients and low δ18OWR values in Early Rhyolites from plv-1 are attributed to an active hydrothermal aquifer that has descended slightly from earlier, shallower elevations. Similarly, severe 18O depletions in Bishop Tuff samples from the idfu 44-16 and rdo-8 wells reflect active convection beneath the western moat, whereas milder 18O depletions in Early Rhyolites from mlgrap-1 were apparently caused by hydrothermal alteration at lower temperatures. The O-isotope profiles imply that surface discharge within and around the resurgent dome results from shallow, eastward-directed outflow from a zone of higher enthalpy hydrothermal upflow beneath the western caldera moat. Intrusive magmatic heat source(s) are inferred to exist beneath the western moat, perhaps beneath Mammoth Mountain.  相似文献   

2.
The minerals of basic and acidic rocks from the volcano-sedimentary sequence in the Huelva area, Spain, Iberian Pyrite Belt, display an extendedδ18O enrichment. Quartzδ18O values from quartz-keratophyres vary from +10.5 to +17.0 and feldsparδ18O values from +14.4 to +16.0. For the spilite or spilitized doleritesδ18O values vary from +9.9 to +13.4 for feldspar, from +6.4 to +9.8 for chlorite, from +3.7 to +4.3 for ilmenite and from +13.6 to +14.0 for quartz, but pyroxene exhibits magmatic values, from +5.3 to +6.1 with an exception at +7.5. The chloriteδD values vary from −34 to −43‰.This is attributed to hydrothermal alteration with seawater enriched inδ18O by circulation through sediments.The temperatures of interaction determined from isotopic fractionations between minerals range from 400° to 520°C.CalculatedδD andδ18O values for water in equilibrium with the minerals at isotopic temperatures range from −16 to +5 and from +8.3 to +12.8, respectively.A model of circulation of seawater through a pile of sedimentary rocks and then through basaltic rocks is proposed to explain the high18O compositions of the rocks from the Huelva District. Water/rock mass ratios calculated from this model range between 0.3 and 0.7 for the determined range of temperatures.  相似文献   

3.
Quaternary lavas from the Northern Mariana Islands have respective O- and S-isotope ranges ofδ18O = +5.7 to +6.6 (‰ SMOW) andδ34S = +2.0to+20.7 (‰ CDT). Chemically evolved andesites and dacites with meanδ18O = +6.3 ± 0.2 are slightly enriched in18O with respect to unfractionated basalts of<53%SiO2 with meanδ18O = +6.0 ± 0.1. This18O enrichment can be explained in terms of differentiation of parental mafic magmas havingδ18O values between +5.7 to +6.2‰ through closed-system crystal fractionation because the lavas from all nine islands of the arc define a coherentδ18OSiO2 trend. The S-isotope composition of oxidized magmas is not modified extensively through the degassing of SO2; therefore, the meanδ34S value of ca. +11‰ for the Mariana lavas is considered to be representative of their source region.The enrichment of18O and34S in Mariana Arc parental magmas relative to ocean floor basalts withδ18O ca. + 5.7‰ andδ34S = ca.0.3‰ is attributed to the recycling of18O- and34S-rich crustal components (sediment withδ18O = ca. + 25‰ and seawater sulfate withδ34S = ca. +20‰ into the upper mantle source region for these arc magmas. This interpretation is consistent with enrichments of radiogenic Sr and Pb in the same lavas relative to ocean-floor basalts erupted either side of the arc, which are presumed to share a common upper mantle source. This enrichment is considered to reflect the mixing of two components, one having a typical upper mantle composition and the other having a more radiogenic character similar to that of western Pacific pelagic sediments.  相似文献   

4.
Measurements of stable isotope compositions and water contents of boninite series volcanic rocks from the island of Chichi-jima, Bonin Islands, Japan, confirm that a large amount (1.6–2.4 wt.%) of primary water was present in these unusual magmas. An enrichment of 0.6‰ in18O during differentiation is explained by crystallization of18O-depleted mafic phases. Silicic glasses have elevated δ18O values and relatively low δD values indicating that they were modified by low-temperature alteration and hydration processes. Mafic glasses, on the other hand, have for the most part retained their primary isotopic signatures since Eocene time. Primary δD values of −53 for boninite glasses are higher than those of MORB and suggest that the water was derived from subducted oceanic lithosphere.  相似文献   

5.
Eighteen basic rocks from Ascension Island (South Atlantic) give a mean87Sr/86Sr ratio of 0.70311 ± 17 for both volcanics and plutonic inclusions. The late-stage differentiated rocks (rhyolites and granitic inclusions) have much higher87Sr/86Sr ratios, up to 0.712. All these rocks display the same range of Nd isotopic compositions (εNdvalues from6.9to11.1with a mean on12samples of8.4 ± 0.6) implying a cogenetic relation between the two sequences. The D/H systematics lead to the same conclusion.In the NdSr diagram, the data plot close to the mantle array and show a positive correlation. This suggests a mixing between a depleted MORB-type mantle, i.e. the upper mantle, and a hot-spot with less depleted geochemical characteristics, i.e. the OIB mantle source.The total range of δ18O values lies between 4.8‰ for plagioclase cumulates and 6.7‰ for the most evolved rocks (peralkaline granites and comendites). The basic rocks have values around 5.3‰, typical of mantle-derived material. These oxygen data indicate that the high87Sr/86Sr ratios in the most evolved rocks (both volcanic and plutonic terms) result from the combination of two different processes: incorporation of slight amounts (< 1%) of high-temperature altered oceanic crust by the magma in the late stages of the differentiation process and then in-situ Rb decay since the time of formation of these rocks. Both processes were very effective because of the high Rb and low Sr contents of these evolved rocks.Oxygen isotope systematics in the Ascension Island granites and rhyolites indicate that a fractional crystallization process alone does not produce δ18O values higher than 6.7‰, i.e. that the ultimate δ18O enrichment, relative to the initial basic magma, is not greater than 1.5‰.  相似文献   

6.
Anhydrous spinel lherzolite xenoliths from the Shavaryn-Tsaram volcano, which represent unusually clinopyroxenerich samples of upper mantle beneath the Tariat Depression in north-central Mongolia, have particularly low δ18O values of +4.9 to +5.7‰ SMOW. Constituent minerals exhibit small (ca. 0.5–0.7‰) variations in18O content (olivine = +4.6 to +5.3‰, clinopyroxene = +5.6 to +6.1‰, orthopyroxene = +5.8 to +6.5‰), that are unrelated to xenolith modal mineralogy, chemical composition, radiogenic isotope character, or pyroxene equilibration temperature. This O-isotope character of the Tariat xenoliths is interpreted to reflect the closed-system distribution of oxygen isotopes in a slowly cooling mantle diapir emplaced into the lithosphere from a relatively primitive region of the asthenosphere.  相似文献   

7.
18O/16O and 87Sr/86Sr ratios were determined for Quaternary calc-alkalic volcanic rocks from six volcanic rock suites in the central and western Japan arcs. The δ18O values relative to SMOW and 87Sr/86Sr ratios range from +6.3 to +9.90/00 and 0.70357 to 0.70684, respectively. Both the O- and Sr-isotopic compositions are higher than those for island-arc primitive magmas and their differentiates. The isotopic compositions of the calc-alkalic rocks cannot be derived by a simple fractional crystallization of the primitive magmas. On the other hand, the 18O- and 87Sr-enrichment is confined to the rock suites located in well-developed island arcs having thick continental-type crust with low or negative Bouguer anomalies. Involvement of 18O- and 87Sr-rich crustal material in the magma formation is suggested.The isotopic compositions vary remarkably within individual rock suites as well as from volcano to volcano. The data points in δ18O vs. 87Sr/86Sr plot accord with a mixing model between primitive magmas and crustal material of dioritic composition on an average, assuming their comparative Sr contents. The primitive magmas involved could not be low-Sr tholeiites, but magmas more or less enriched in incompatible elements including Sr, which correspond to high-alkali tholeiites or alkali basalts and their evolved magmas. The nature of the primitive magmas seems to change from tholeiitic to more alkalic with progressing island-arc evolution.Mixing of crust-derived melts is more plausible than assimilation of solid-rocks for involving 20 to 30% crustal material in the magmas along simple mixing curves. Isotopic variations between the rock suites are ascribed to variable Sr concentration radio of the end-members, variable isotopic compositions of crustal material or variable mixing ratio of the end-members. Extremely high-δ 18O rocks with moderate increase in 87Sr/86Sr ratio suggest another mixing process in shallower magma chambers between andesite magmas and metasedimentary rocks having high δ 18O and 87Sr/86Sr values but low Sr content. Subsequent fractional crystallization of once-derived magmas would be the prominent process for the rock suites showing gradual increase in 18O up to 10/00 with uniform 87Sr/86Sr ratios.  相似文献   

8.
The Campi Flegrei (Naples, Campanian Plain, southern Italy) geothermal system is hosted by Quaternary volcanic rocks erupted before, during and after the formation of the caldera that represents one of the major structural features in the Neapolitan area. The volcanic products rest on a Mesozoic carbonate basement, cropping out north, east and south of the area. Chemical (major, minor and trace elements) and stable isotope (C, H, O) analyses were conducted on drill-core samples recovered from geothermal wells MF-1, MF-5, SV-1 and SV-3, at depths of ˜ 1100 to 2900 m. The study was complemented by petrographic and SEM examination of thin sections. The water which feeds the system is both marine and meteoric in origin. Mineral zonation typical of a high-temperature geothermal system exists in all the geothermal wells; measured temperatures in wells are as high as ˜ 400 °C. The chemical composition of the waters suggests the existence of two reservoirs: a shallow reservoir (depth < 2000 m) fed by seawater that boiled at 320 °C and became progressively diluted by steam-heated local meteoric water during its ascent; and a deeper reservoir (depth > 2000 m) of hypersaline water. The drill-cores are mainly hydrothermally altered volcanics of trachy-latitic affinity, but some altered pelites and limestones are also present. Published Na, Mg and K concentrations of selected geothermal waters indicate that the hydrothermal fluids are in equilibrium with their host rocks, with respect to K-feldspar, albite, sericite and chlorite. The measured δ18O(SMOW) values of rocks range from +4.3 to + 16.5%. The measured δD(SMOW) values range from − 79 to − 46%. The calculated isotopic composition of the fluids at equilibrium with the samples vary from + 1 to + 8.3%. δ18O and from − 52 to + 1%. δD. The estimated isotopic composition of the waters at equilibrium with the studied samples confirmed the existence of two distinct fluid types circulating in the geothermal system. The shallower has a marine water signature, while the deeper water has a signature consistent both with magmatic and meteoric origins. In the latter case, the recharge of this aquifer likely occurs at the outcrop of the Mesozoic Limestones surrounding the Campanian Plain; after infiltration, the water percolates through evaporitic layers, becoming hypersaline and D-depleted.  相似文献   

9.
During 1979–1989, variations were observed in the oxygen composition of the water contained in the geothermal reservoir at Vulcano Island, Italy.The reservoir water, that has a magmatic origin, showed an oxygen composition of +1.0±0.5‰ δ18O during periods without local tectonic earthquakes, and an oxygen composition of +3.4±0.5‰ δ18O after the highest-energy seismic activity that occurred recently near the island. A slight increase of the δ18O value in the reservoir water was also observed after a low-energy sequence of tectonic earthquakes that occurred at very shallow depth just beneath Vulcano Island. These 18O variations in the reservoir water are consistent with earthquake-induced increases in the contribution from high-temperature δ18O-rich magmatic condensate to the geothermal reservoir, and with subsequent decreases in the δ18O value due to 18O exchanges at the temporarily increased reservoir temperature during reactions between the highly reactive magmatic condensate and the local rocks.Only minor changes in the deuterium composition of the reservoir water occurred with time, as the δD value in the magmatic condensate released from the magma after major local earthquakes quickly approached the δD value of the water contained in the geothermal reservoir.Also the chloride concentration in the reservoir water appears to be linked to the contribution from the magmatic fluid. This chloride content seems not to have undergone major changes with time, as it may be buffered by temporary increases in the reservoir temperature up to values >300°C induced by major local earthquakes. This mechanism may possibly occur also in other magmatic–hydrothermal systems.  相似文献   

10.
It is well known that the destruction of the North China Carton(NCC) is closely related to subduction of the PaleoPacific slab, but materials recording such subduction has not been identified at the peak time of decratonization. This paper presents data of whole-rock major and trace elements and Sr-Nd-Hf isotopes and zircon U-Pb ages and Hf-O isotopes for Mesozoic volcanic rocks from the Liaodong-Jinan region in the northeastern NCC, in order to trace the subduction-related materials in their source and origin. The Mesozoic volcanic rocks in the Liaodong-Jinan region are mainly composed of two series of rocks, including alkaline basaltic trachyandesite, trachyandesite and trachyte, and subalkaline trachyandesite and andesite. Zircon U-Pb dating yields eruption ages of 129–124 Ma for these rocks. The Early Cretaceous volcanic rocks are all enriched in LILEs(such as Rb, Sr, Ba and Th) and LREEs, depleted in HFSEs(such as Nb, Ta and Ti), indicating that they were originated from mantle sources that had been modified by subducted crustal materials. However, they have relatively heterogeneous and variable isotopic compositions. The alkaline basaltic trachyandesite, trachyandesite and trachyte have enriched whole-rock Sr-Nd-Hf and zircon Hf isotopic compositions and mantle-like δ~(18)O values, suggesting that they were derived from low-degree partial melting of an isotopically enriched lithospheric mantle source. In contrast, the subalkaline trachyandesite and andesite have relatively depleted isotopic compositions with zircon ε_(Hf)(t) values up to +5.2 and heavy zircon O isotopic compositions with δ~(18)O values of +8.1‰ to +9.0‰, indicating that they were originated from a lithospheric mantle source that had been metasomatized by melts/fluids derived from the recycled low-T altered oceanic basalt. All of these geochemical features suggest that the Early Cretaceous volcanic rocks in the Liaodong-Jinan region would result from mixing of mafic magmas with different compositions. Such magmas were originated from the enriched lithospheric mantle and the young metasomatized mantle, respectively, with variable extents of enrichment and depletion in trace elements, radiogenic isotopes and O isotopes. Importantly, the identification of the low-T altered oceanic crust component in the origin of Early Cretaceous volcanic rocks by the zircon Hf-O isotopes provides affirmative isotopic evidence and direct material records for Mesozoic subduction of the Paleo-Pacific slab that induced decratonization of the North China Craton.  相似文献   

11.
The Long Valley Exploratory Well, at the center of the Resurgent Dome of Long Valley caldera, penetrated pre-caldera basement rocks at a depth of 2101.72–2313.0 m, beneath the caldera-forming Bishop Tuff and post-caldera Early Rhyolite. The basement rocks contain prominent quartzites, with ubiquitous milky white quartz veins (with minor calcite and pyrite) and fractures of varied orientation and geometry. The other members of the basement sequence are very fine-grained quartz-rich graphitic pelites with calcite veins, spotted hornfels, and shallow intrusive rocks. Previous studies established the presence of a post-caldera, paleohydrothermal system (500–100 ka) to a depth of 2000 m that affected the Bishop Tuff and a recent (40 ka to present) hydrothermal system at shallow depth (<1 km). The deeper extent of these hydrothermal activities is established in this paper by a detailed oxygen isotope analysis of the drill core samples. 238 analyses of δ18O in 50 quartz veins within the 163.57 m depth interval of basement rocks reveal extreme heterogeneity in δ18O values (8–19.5‰). Majorities of the 84 bulk analyses of quartzites show variation of δ18O within a narrow range of 14–16‰. However, certain samples of these quartzites near the contacts with veins and fractures exhibit sharp drops in δ18O. The interbedded pelitic rocks and spotted hornfels have whole-rock δ18O ranging from 2.2 to 11.8‰. Clear, euhedral vuggy quartz that partially fills earlier open fractures in both the quartzites and quartz veins, has distinctive δ18O, ranging between −3.2 and +8.4‰. Low values of δ18O are also found in the hydrothermal minerals and whole rocks adjacent to the thin veins, clearly indicating infiltration of meteoric water. Three distinct observed patterns of fractionation in δ18O between veins and host quartzites are analyzed with the principles of mass balance, equilibrium oxygen isotope fractionation in closed system, and kinetically controlled oxygen isotope exchange in an open system. This analysis suggests that the early quartz veins formed due to a magmatic-hydrothermal activity with no influx of external water once the system comprising the sedimentary envelope and a magmatic-hydrothermal fluid phase became closed. Two-stage isotopic exchange processes caused fractionation in the δ values that originally formed arrays with slope 1 in a δvein quartz–δhost quartzite space. Another array in the same space, with near zero slope was also formed due to variation in temperature, initial isotopic compositions of the quartzite sequence and the fluid phase. Variation in temperature was mostly in the range of 300–400°C giving Δ (=δvein quartz–δhost quartzite)≈−2.8 to +2.8. The δ18O of the fluid could range from −5 to +10; however a narrower range of +5 to +10 can explain the data. This episode of hydrothermal activity could take place either as a single pulse or in multiple pulses but each as a closed system. A later, fracture-controlled, meteoric water (δ18O−0.46 to −12.13) flow and interaction (at 250°C) is interpreted from the analysis of δ18O values of the coexisting quartz and calcite pairs and existence of markedly 18O-depleted pelitic horizons interbedded with 18O-enriched quartzite layers. Thus, the interpreted earlier magmatic-hydrothermal activity was overprinted by a later meteoric-hydrothermal activity that resulted in steep arrays of δ18O values in the δvein quartz–δhost quartzite space. Calculations show that the likely life span of the post-caldera, hydrothermal activity in the depth range of 2.1–2.3 km beneath Long Valley was 0.08–0.12 Ma. Diffusive ±advective transport of oxygen isotopes from fracture-channelized meteoric water to nearly impermeable wall rocks caused a lowering of δ18O values in the quartz over short distances and in calcites over greater distances. Thus, the hydrothermal activity appears pervasive even though the meteoric water flow was primarily controlled by fractures.  相似文献   

12.
The chemical composition and D/H, and ratios have been determined for the acid hot waters and volcanic gases discharging from Zaō volcano in Japan. The thermal springs in Zaō volcano issue acid sulfate-chloride type waters (Zaō) and acid sulfate type waters (Kamoshika). Gases emitted at Kamoshika fumaroles are rich in CO2, SO2 and N2, exclusive of H2O. Chloride concentrations and oxygen isotope data indicate that the Zaō thermal waters issue a fluid mixture from an acid thermal reservoir and meteoric waters from shallow aquifers. The waters in the Zaō volcanic system have slight isotopic shifts from the respective local meteoric values. The isotopic evidence indicates that most of the water in the system is meteoric in origin. Sulfates in Zaō acid sulfate-chloride waters with δ34S values of around +15‰, are enriched in 34S compared to Zaō H2S, while the acid sulfate waters at Kamoshika contain supergene light sulfate (δ34S = + 4‰) derived from volcanic sulfur dioxide from the volcanic exhalations. The sulfur species in Zaō acid waters are lighter in δ34S than those of other volcanic areas, reflecting the difference in total pressure.  相似文献   

13.
The Lower Pliocene volcanic rocks occurring in the Gölcük area of SW Turkey exhibit alkaline major element trends with a general potassic character. The development of volcanism can be divided into 2 major stages such as trachytic ancient lavas/domes and tephriphonolitic, trachyandesitic to trachytic Gölcük eruptions (ignimbrites, lava/dome extrusions, phreatomagmatic deposits, and finally, young domes). Volcanic rocks consist primarily of plagioclase, clinopyroxene (which ranges in composition from diopside to augite and are commonly zoned), biotite, and phlogopite. Amphibole phenocrysts are restricted to the pyroclastic deposits. Pseudoleucites are also seen only in the lava/dome extrusions. Oxides and apatites are common accessory phenocryst phases. As would be expected from their potassic–alkaline nature, the volcanic rocks of the Gölcük area contain high amounts of LILE (Ba, Sr, Rb and K), LREE, and Zr. Concentrations of compatible elements such as Cr, Ni and V are very low, possibly indicating fractionation of olivine and clinopyroxene. Correlation of SiO2, Rb/Sr and MgO with 87Sr/86Sr (0.703506–0.704142) exhibit an increasing trend in the direction of crustal contamination. However, the isotopic compositions of Sr are not as high to indicate a high level of crustal contamination. Geochemical data are consistent with the derivation of Gölcük volcanic rocks from a metasomatized and/or enriched lithospheric mantle source during crustal extension in the area. This metasomatism was probably occurred by fluids released from the northward subduction between African and Eurasian plates during Tertiary, as the Gölcük volcanic rocks display features of island-arc magmas with having high Ba/Nb (>28) ratios, and Nb and Ti depletions. Lower Pliocene volcanism in the Gölcük was response to extensional tectonics.  相似文献   

14.
Recent, fresh, volcanic rocks of the intra-oceanic Mariana and Volcano Arcs were analyzed for O and Sr isotopic compositions in order to determine the source of these magmas. Fresh, non-arc, volcanic rocks from the regions surrounding the Mariana-Volcano Arcs and some DSDP sediments were also analyzed for comparison. The oxygen isotopic ratios of the arc lavas (5.5–6.8‰) exhibited a small inter-island variation that cannot be entirely explained by fractional crystallization. The Sr isotopic composition of the arc lavas is remarkably uniform (0.70332–0.70394 for the Marianas). Three models are considered in order to explain the observed isotopic characteristics: (1) bulk mixing and melting of MORB-type mantle with (a) subducted sediments, and (b) subducted oceanic crust (excluding sediments); (2) melting of a mixture of sediment-derived fluids and MORB-type mantle; and (3) melting of a mixture of sediment-derived fluids and oceanic island or “hot-spot” type mantle. The last model fits the data best. The conclusion that very small, and variable, amounts of sediment-derived fluid ( 1%) are required to explain the observed inter-island O isotopic variation, is consistent with that of other workers who used different isotopic and trace element methods. The generation of magmas in the Mariana-Volcano Arcs involves very little sediment and the source region of Mariana lavas is isotopically indistinguishable from that of hot-spot basalts.  相似文献   

15.
Isotopic compositions were determined for hydrothermal quartz, calcite, and siderite from core samples of the Newberry 2 drill hole, Oregon. The δ15O values for these minerals decrease with increasing temperatures. The values indicate that these hydrothermal minerals precipitated in isotopic equilibrium with water currently present in the reservoirs. The δ18O values of quartz and calcite from the andesite and basalt flows (700–932 m) have isotopic values which require that the equilibrated water δ18O values increase slightly (− 11.3 to −9.2‰) with increasing measured temperatures (150–265°C). The lithic tuffs and brecciated lava flows (300–700 m) contain widespread siderite. Calculated oxygen isotopic compositions of waters in equilibrium with siderite generally increase with increasing temperatures (76–100°C). The δ18O values of siderite probably result from precipitation in water produced by mixing various amounts of the deep hydrothermal water (− 10.5 ‰) with meteoric water (− 15.5 ‰) recharged within the caldera. The δ13C values of calcite and siderite decrease with increasing temperatures and show that these minerals precipitated in isotopic equilibrium with CO2 of about −8 ‰.The δ18O values of weakly altered (<5% alteration of plagioclase) whole-rock samples decrease with increasing temperatures above 100°C, indicating that exchange between water and rock is kinetically controlled. The water/rock mass ratios decrease with decreasing temperatures. The δ18O values of rocks from the bottom of Newberry 2 show about 40% isotopic exchange with the reservoir water.The calculated δ18O and δD values of bottom hole water determined from the fluid produced during the 20 hour flow test are −10.2 and −109‰, respectively. The δD value of the hydrothermal water indicates recharge from outside the caldera.  相似文献   

16.
Abstract The Solund‐Stavfjord ophiolite complex (SSOC) in western Norway represents a remnant of the Late Ordovician oceanic lithosphere, which developed in an intermediate‐ to fast‐spreading Caledonian back‐arc basin. The internal architecture and magmatic features of its crustal component suggest that the SSOC has a complex, multistage sea floor spreading history in a supra‐subduction zone environment. The youngest crustal section associated with the propagating rift tectonics consists of a relatively complete ophiolite pseudostratigraphy, including basaltic volcanic rocks, a transition zone between the sheeted dyke complex and the extrusive sequence, sheeted dykes, and high‐level isotropic gabbros. Large‐scale variations in major and trace element distributions indicate significant remobilization far beyond that which would result from magmatic processes, as a result of the hydrothermal alteration of crustal rocks. Whereas K2O is strongly enriched in volcanic rocks of the extrusive sequence, Cu and Zn show the largest enrichment in the dyke complex near the dyke–volcanic transition zone or within this transition zone. The δ18O values of the whole‐rock samples show a general depletion structurally downwards in the ophiolite, with the largest and smallest variations observed in volcanic rocks and the transition zone, respectively. δ18O values of epidote–quartz mineral pairs indicate 260–290°C for volcanic rocks, 420°C for the transition zone, 280–345°C for the sheeted dyke complex and 290–475°C for the gabbros. The 87Sr/86Sr isotope ratios show the widest range and highest values in the extrusive rocks (0.70316–0.70495), and generally the lowest values and the narrowest range in the sheeted dyke complex (0.70338–0.70377). The minimum water/rock ratios calculated show the largest variations in volcanic rocks and gabbros (approximately 0–14), and generally the lowest values and range in the sheeted dyke complex (approximately 1–3). The δD values of epidote (?1 to ?12‰), together with the δ18O calculated for Ordovician seawater, are similar to those of present‐day seawater. Volcanic rocks experienced both cold and warm water circulation, resulting in the observed K2O‐enrichment and the largest scatter in the δ18O values. As a result of metal leaching in the hot reaction zone above a magma chamber, Zn is strongly depleted in the gabbros but enriched in the sheeted dyke complex because of precipitation from upwelling of discharged hydrothermal fluids. The present study demonstrates that the near intact effect of ocean floor hydrothermal activity is preserved in the upper part of the SSOC crust, despite the influence of regional lower greenschist facies metamorphism.  相似文献   

17.
Stable isotope compositions (δD, δ18O and δ34S) of volcanic lake waters, gas condensates and spring waters from Indonesia, Italy, Japan, and Russia were measured. The spring fluids and gas samples plot in a broad array between meteoric waters and local high-temperature volcanic gas compositions. The δD and δ18O data from volcanic lakes in East Indonesia plot in a concave band ranging from local meteoric waters to evaporated fluids to waters heavier than local high-temperature volcanic gases. We investigated isotopic fractionation processes in volcanic lakes at elevated temperatures with simultaneous mixing of meteoric waters and volcanic gases. An elevated lake water temperature gives enhanced kinetic isotope fractionation and changes in equilibrium fractionation factors, providing relatively flat isotope evolution curves in δ18O–δD diagrams. A numerical simulation model is used to derive the timescales of isotopic evolution of crater lakes as a function of atmospheric parameters, lake water temperature and fluxes of meteoric water, volcanic gas input, evaporation, and seepage losses. The same model is used to derive the flux magnitude of the Keli Mutu lakes in Indonesia. The calculated volcanic gas fluxes are of the same order as those derived from energy budget models or direct gas flux measurements in open craters (several 100 m3 volcanic water/day) and indicate a water residence time of 1–2 decades. The δ34S data from the Keli Mutu lakes show a much wider range than those from gases and springs, which is probably related to the precipitation of sulfur in these acid brine lakes. The isotopic mass balance and S/Cl values suggest that about half of the sulfur input in the hottest Keli Mutu lake is converted into native sulfur.  相似文献   

18.
The Ischia geothermal system is hosted by silicic rocks of the Quaternary Potassic Roman Province, in southern Italy. Exploration drilling down to 1156 m depth in the mid-1950s provided information on boiling profiles (up to 250°C) and on the depth and permeability of the potential reservoirs. Discharge fluid samples were collected and analyzed to define the inflow of surrounding seawater (C1 ranges from 2.5 to 20 g/kg) into the system.Analyses of samples from surface manifestations and shallow wells collected during 1983 and 1988 point to the existence of three distinct mixing regimes, involving three water components. A dishomogeneous body of diluted water (Cl less than 2.5 g/kg), that occurs at depths > 700 m and reequilibrates at 240°C at least, is overlain by an aquifer of groundwater variably mixed with variably seawater (Cl from 4 to 10 g/kg), which tends to reequilibrate at 160°C. Steam-heated waters locally develop and act as dilutants of the rising geothermal fluids.Dilution, mixing, and evaporation of the ascending chloride fluids are supported by oxygen and hydrogen isotopic data the thermal waters being enriched in 18O and D with respect to local meteoric water by up to 7 and 30‰, respectively. The relative composition of the major cations in thermal solutions was used to discriminate the two main groups of thermal waters, the reservoir temperatures of which are estimated from the Na/K-gethermometer. K-Mg geothermometer indicates reequilibration in near-surface conditions.The isotopic composition of the fumarolic steam varies from −7 to −12‰ in ∂8O and from − 35 to − 70‰ in ∂D, in agreement with a deep mixed fluid that boils adiabatically from 240 to 80°C. The deuterium content of the H2O-H2 pair gives enrichment factor of about 830‰, corresponding to equilibrium temperature conditions slightly higher than the surface boiling temperatures. The ∂13C of CO2is almost constant at −4.5‰ (1δ=0.4), suggesting an important magmatic contribution, and the ∂18O values of CO2appears to in equilibrium with accompanying steam at the measured temperatures.The CO2/Ar and H2/Ar chemical ratios have been used to derive aquifer temperatures, the values obtained being consistent with those of solute geothermometers.  相似文献   

19.
Examples of positive correlations between initial 87Sr/86Sr and δ18O have now been shown to be very common in igneous rock series. These data in general require some type of mixing of mantle-derived igneous rocks with high-18O, high-87Sr crustal metamorphic rocks that once resided on or near the Earth's surface, such as sedimentary rocks or hydrothermally altered volcanic rocks. Mixing that involves assimilation of country rocks by magmas, however, is not a simple two-end-member process; heat balance requires appreciable crystallization of cumulates. In such cases, the isotopic compositions may strongly reflect this open-system behavior and indicate the process of assimilation, whereas the major element chemical compositions of the contaminated magmas will be largely controlled by crystal-melt equilibria and crystallization paths fixed by multicomponent cotectics. A variety of oxygen and strontium isotope “mixing” curves were therefore calculated for this process of combined assimilation-fractional crystallization. The positions and characteristics of the resultant curves on δ18O-87Sr/86Sr diagrams markedly diverge from simple two end-member mixing relationships. Based on the above, model calculations can be crudely fitted to two igneous rock suites (Adamello and Roccamonfina in Italy), but the shapes of the calculated curves appear to rule out magmatic assimilation as an explanation for most δ18O-87Sr/86Sr correlations discovered so far, including all of those involving calc-alkaline granitic batholiths and andesitic volcanic rocks. The isotopic relationships in such magma types must be inherited from their source regions, presumably reflecting patterns that existed in the parent rocks (or magmas) prior to or during melting.  相似文献   

20.
Cenozoic volcanism in the Great Basin is characterized by an outward migration of volcanic centers with time from a centrally located core region, a gradational decrease in the initial Sr87/Sr86 ratio with decreasing age and increasing distance from the core, and a progressive change from calc-alkalic core rocks to more alkalic basin margin rocks. Generally each volcanic center erupted copious silicic ignimbrites followed by small amounts of basalt and andesite. The Sr82/Sr86 ratio for old core rocks is about 0.709 and the ratio for young basin margin rocks is about 0.705. Spatially and temporally related silicic and mafic suites have essentially the same Sr87/Sr86 ratios. The locus of older volcanism of the core region was the intersection of a north-south trending axis of crustal extension and high heat flow with the northeast trending relic thermal ridge of the Mesozoic metamorphic hinterland of the Sevier Orogenic Belt. Derivation of the Great Basin magmas directly from mantle with modification by crustal contamination seems unlikely. Initial melting of lower crustal rocks probably occurred as a response to decrease in confining pressure related to crustal extension. Volcanism was probably also a consequence of the regional increase in the geothermal gradient that is now responsible for the high heat flow of the Basin and Range Province. High Sr isotopic ratios of the older core volcanic rocks suggests that conditions suitable for the production of silicic magmas by partial fusion of the crust reached higher levels within the crust during initial volcanism than during production of later magmas with lower isotopic ratios and more alkaline chemistry. As the Great Basin became increasingly attenuated, progressively lower portions of the crust along basin margins were exposed to conditions suitable for magma genesis. The core region became exhausted in low temperature melting components, and volcanism ceased in the core before nearby areas had completed the silicic-mafic eruption cycle leading to their own exhaustion of crustal magma sources.  相似文献   

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