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1.
DSDP Hole 504B is the deepest basement hole in the oceanic crust, penetrating through a 571.5 m pillow section, a 209 m lithologic transition zone, and 295 m into a sheeted dike complex. An oxygen isotopic profile through the upper crust at Site 504 is similar to that in many ophiolite complexes, where the extrusive section is enriched in 18O relative to unaltered basalts, and the dike section is variably depleted and enriched. Basalts in the pillow section at Site 504 haveδ 18O values generally ranging from +6.1 to +8.5‰ SMOW(mean= +7.0‰), although minor zeolite-rich samples range up to 12.7‰. Rocks depleted in 18O appear abruptly at 624 m sub-basement in the lithologic transition from 100% pillows to 100% dikes, coinciding with the appearance of greenschist facies minerals in the rocks. Whole-rock values range to as low as +3.6‰, but the mean values for the lithologic transition zone and dike section are +5.8 and +5.4‰, respectively. Oxygen and carbon isotopic data for secondary vein minerals combined with the whole rock data provide evidence for the former presence of two distinct circulation systems separated by a relatively sharp boundary at the top of the lithologic transition zone. The pillow section reacted with seawater at low temperatures (near 0°C up to a maximum of around 150°C) and relatively high water/rock mass ratios (10–100); water/rock ratios were greater and conditions were more oxidizing during submarine weathering of the uppermost 320 m than deeper in the pillow section. The transition zone and dikes were altered at much higher temperatures (up to about 350°C) and generally low water/rock mass ratios ( 1), and hydrothermal fluids probably contained mantle-derived CO2. Mixing of axial hydrothermal fluids upwelling through the dike section with cooler seawater circulating in the overlying pillow section resulted in a steep temperature gradient ( 2.5°C/m) across a 70 m interval at the top of the lithologic transition zone. Progressive reaction during axial hydrothermal metamorphism and later off-axis alteration led to the formation of albite- and Ca-zeolite-rich alteration halos around fractures. This enhanced the effects of cooling and18O enrichment of fluids, resulting in local increases inδ18O of rocks which had been previously depleted in18O during prior axial metamorphism. 相似文献
2.
The meteorite ALH84001, a sample of the ancient martian crust, contains small quantities (1%) of strongly chemically zoned carbonate. High spatial resolution (10 μm) ion microprobe analyses show that the chemical zoning is strongly correlated with variations in oxygen isotope ratios. Early formed Ca,Fe-rich cores have δ 18O 7‰ increasing to 22‰ SMOW in the more Mg-rich outer cores and magnesite rims. Isolated areas of ankerite appear to be isotopically lighter with δ 18O 1‰. The large range in δ 18O requires a significant range in either fluid isotopic composition, or temperature, or both, in the course of the deposition sequence. Our data are inconsistent with formation of the zoned carbonates by closed system Rayleigh fractionation. There is no unique interpretation of the oxygen data, but the recent observation of existence of Δ 17O excesses in the carbonate appears to rule out models which involve high temperature isotopic exchange with silicate. Comparison with terrestrial analogues suggests that ALH84001 carbonates formed in a hydrothermal system with T<400°C, and which, at least in the early stages of formation, may have involved water with δ 18O < 0‰ SMOW. The later stages of deposition probably occurred at temperatures below 150°C, a conclusion which does not preclude the co-existence of thermophilic bacteria; temperatures during earlier stages of deposition are less likely to have been hospitable to bacteria. 相似文献
3.
The modified increment method has been applied to the calculation of oxygen isotope fractionation factors for hydroxyl-bearing silicate minerals. The order of 18O enrichment obtained in common rock-forming minerals is: pyrophyllite > kaolinite > tourmaline talc > prehnite topaz > illite > phengite > lepidolite muscovite staurolite > epidote > glaucophane > serpentine chlorite > tremolite > hornblende > phlogopite biotite > humite > norbergite > ilvaite. Hydroxyl-bearing silicates are enriched in 18O relative to hydroxyl groups but depleted in 18O relative to anhydrous counterparts. Three sets of self-consistent fractionation factors: between quartz and the hydroxyl-bearing silicate minerals, between calcite and the silicate minerals, and between the silicate minerals and water, have been calculated for a temperature range of 0–1200°C. The fractionation factors calculated for mineral pairs are applicable to isotopic geothermometry in igneous, metamorphic and sedimentary petrology. They can be used as a test of isotopic equilibrium or disequilibrium in natural mineral assemblages over all temperature ranges of geological interest. The difference in oxygen isotope composition between the hydroxyl-bearing mineral and the OH group is quantitatively demonstrated to be temperature dependent and, therefore, can be used as a single-mineral geothermometer. 相似文献
4.
Rocks of the Miocene Macquarie Island ophiolite, south of New Zealand, have oxygen and carbon isotopic compositions comparable to those of seafloor rocks. Basalt glass and weathered basalts have δ 18O values at 5.8–6.0‰ and 7.9–9.5‰, respectively, similar to drilled seafloor rocks including samples from the Leg 29 DSDP holes near Macquarie Island. Compared to the basalt glass, the greenschist to amphibolite facies metaintrusives are depleted in 18O (δ 18O=3.2–5.9‰) similar to dredged seafloor samples, whereas the metabasalts are enriched (δ 18O=7.1–9.7‰). Although the gabbros are only slightly altered in thin-section they have exchanged oxygen with a hydrothermal fluid to a depth of at least 4.5 km. There is an approximate balance between 18O depletion and enrichment in the exposed ophiolite section. The carbon isotopic composition of calcite in the weathered basalts (δ 13C=1.0–2.0‰) is similar to those of drilled basalts, but the metamorphosed rocks have low δ 13C values (?14.6 to 0.9‰).These data are compatible with two seawater circulation regimes. In the upper regime, basalts were weathered by cold seawater in a circulation system with high water/rock ratios (?1.0). Based on calcite compositions weathering temperatures were less than 20°C and the carbon was derived from a predominantly inorganic marine source. As previously suggested for the Samail ophiolite, it is postulated that the lower hydrothermal regime consisted of two coupled parts. At the deeper levels, seawater circulating at low water/rock ratios (0.2–0.3) and high temperatures (300–600°C) gave rise to 18O-depleted gabbro and sheeted dikes via open system exchange reactions. During reaction the seawater underwent a shift in oxygen isotopic composition (δ 18O=1.0–5.0‰) and subsequently caused 18O enrichment of the overlying metabasalts. In the shallower part of the hydrothermal regime the metabasalts were altered at relatively high water/rock ratios (1.0–10.0) and temperatures in the range 200–300°C. The relatively low water/rock ratios in the hydrothermal regime are supported by the low δ 13C values of calcite, interpreted as evidence of juvenile carbon in contrast to the inorganic marine carbon found in the weathered basalts. 相似文献
5.
Laboratory culturing experiments with living Globigerina bulloides indicate that Mg/Ca is primarily a function of seawater temperature and suggest that Mg/Ca of fossil specimens is an effective paleotemperature proxy. Using culturing results and a core-top Neogloboquadrina pachyderma calibration, we have estimated glacial–interglacial changes in sea surface temperature (SST) using planktonic Mg/Ca records from core RC11-120 in the Subantarctic Indian Ocean (43°S, 80°E) and core E11-2 in the Subantarctic Pacific Ocean (56°S, 115°W). Our results suggest that glacial SST was about 4°C cooler in the Subantarctic Indian Ocean and 2.5°C cooler in the Subantarctic Pacific. Comparison of SST and planktonic δ 18O records indicates that changes in SST lead changes in δ 18O by on average 1–3 kyr. The glacial–interglacial temperature change indicated by the Subantarctic Mg/Ca records suggests that temperature accounts for 40–60% of the foraminiferal δ 18O change. We have used the Mg/Ca-based SST estimates and δ 18O determinations to generate site-specific seawater δ 18O records, which suggest that seawater δ 18O was on average 1‰ more positive during glacial episodes compared with interglacial episodes. 相似文献
6.
Geochemical variations in mid-ocean ridge basalts have been attributed to differing proportions of compositionally distinct mantle components in their sources, some of which may be recycled crust. Oxygen isotopes are strongly fractionated by near-surface interactions of rocks with the hydrosphere, and thus provide a tracer of near-surface materials that have been recycled into the mantle. We present here oxygen isotope analyses of basaltic glasses from the mid-Atlantic ridge south of and across the Azores platform. Variations in δ 18O in these samples are subtle (range of 0.47‰) and may partly reflect shallow fractional crystallization; we present a method to correct for these effects. Relatively high fractionation-corrected δ 18O in these samples is associated with geochemical indices of enrichment, including high La/Sm, Ce/Pb, and 87Sr/ 86Sr and low 143Nd/ 144Nd. Our results suggest two first-order conclusions about these enriched materials: (1) they are derived (directly or indirectly) from recycled upper oceanic crustal rocks and/or sediments; and (2) these materials are present in the north Atlantic MORB sources in abundances of less than 10% (average 2–5%). Modeling of variations of δ 18O with other geochemical variables further indicates that the enriched component is not derived from incorporation of sediment or bulk altered oceanic crust, from metasomatism of the mantle by hydrous or carbonate-rich fluids, or from partial melting of subducted sediment. Instead, the data appear to require a model in which the enriched component is depleted mantle that has been metasomatized by small-degree partial melts of subducted, dehydrated, altered oceanic crust. The age of this partial melting is broadly constrained to 250 Ma. Reconstructed plate motions suggest that the enriched component in the north Atlantic mantle may have originated by subduction along the western margin of Pangea. 相似文献
7.
This paper presents new O and Sr isotope data for lavas from the northern part of the Roman perpotassic province. The samples comprise the tephritic leucititic to leucite phonolitic lavas and the saturated lavas from the Vulsinian District, the olivine leucite melilitite of San Venanzo, and the kalsilite diopside melilitite of Cupaello. Previous oxygen isotope work on the lavas of the Vulsinian District suggested crustal contamination of “normal” mantle-derived magmas. The new data cover the ranges previously found. O and Sr isotope ratios of evolved lavas of the undersaturated suite indicate assimilation in variable amounts of up to ca. 10% of continental crustal material. The saturated lavas probably assimilated large amounts (up to ca. 50%) of crust. Lavas chemically identified as corresponding to little modified mantle-derived liquids are high in both 87Sr/ 86Sr andδ 18O: 0.7103−0.7107, +7.8 to +9.4 (Vulsini), 0.7104, +12.3 (San Venanzo) and 0.7112, +14.4 (Cupaello). These high values are interpreted to have been inherited from a metasomatized parental mantle. Hydrous fluids enriched in large-ion lithophile elements and high inδ 18O and 87Sr/ 86Sr are thought to have mixed with mantle of “normal”δ 18O and 87Sr/ 86Sr. The fluids probably origi dehydration of continent-derived sediments, which were subducted beneath a mantle wedge in the continent-continent collision of the Corsica-Sardinia block and the Adriatic (Italian) plate. This hypothesis is supported by Pb and Nd isotopic evidence and is probably valid for the entire Roman Province. 相似文献
8.
Hanford Loam, from Richland, Washington, was used as a test soil to determine the precision, accuracy and nature of two methods to extract soil water for stable isotopic analysis: azeotropic distillation using toluene, and simple heating under vacuum. The soil was oven dried, rehydrated with water of known stable isotopic compositions, and the introduced water was then extracted. Compared with the introduced water, initial aliquots of evolved water taken during a toluene extraction were as much as 30 ‰ more depleted in D and 2.7 ‰ more depleted in 18O, whereas final aliquots were as much as 40 ‰ more enriched in D and 14.3 ‰ more enriched in 18O. Initial aliquots collected during the vacuum/heat extraction were as much as 64 ‰ more depleted in D and 8.4 ‰ more depleted in 18O than was the introduced water, whereas the final aliquots were as much as 139 ‰ more enriched in D, and 20.8 ‰ more enriched in 18O. Neither method appears quantitative; however, the difference in stable isotopic composition between the first and last aliquots of water extracted by the toluene method is less than that from the vacuum/heat method. This is attributed to the smaller fractionation factors involved with the higher average temperatures of distillation of the toluene. The average stable isotopic compositions of the extracted water varied from that of the introduced water by up to 1.4 ‰ in δD and 4.2 ‰ in δ18O with the toluene method, and by 11.0 ‰ in δD and 1.8 ‰ in δ18O for the vacuum/heat method. The lack of accuracy of the extraction methods is thought to be due to isotopic fractionation associated with water being weakly bound (not released below 110°C) in the soil. The isotopic effect of this heat-labile water is larger at low water contents (3.6 and 5.2% water by weight) as the water bound in the soil is a commensurately larger fraction of the total. With larger soilwater contents the small volume of water bound with an associated fractionation is not enough to affect the remaining unbound introduced soil water. Pretreatment of the soil to equilibrate the heat-labile water to the test water produced good results for the toluene distillation but not the vacuum/heat extraction method. Vapors collected over the soils also show stable isotopic variations related to soilwater content. These vapors also appear to be in closer equilibrium with the free water, as extracted by the toluene method, than with the originally introduced water; thus, the soil vapors do not appear to be isotopically affected by the heat-labile water. The toluene method appears to be better for extracting soil water for stable isotopic analysis because it allows more precise temperature control and excludes the extraction of heat-labile water which is isotopically fractionated. The bound nature of this heat-labile water limits association with the hydrologically active soil water; thus, the exclusion of this water from the soil water attained by toluene distillation may be advantageous. However, the azeotropic nature of toluene distillation affords no benefit and the extraction procedure must continue to completion. 相似文献
9.
New oxygen isotope data are presented for submarine lavas erupted close to the transition between the oceanic Kermadec island arc and the continental Taupo Volcanic Zone, New Zealand. Volcanic glasses display δ 18O values ranging from +5.65‰ to +5.83‰, clinopyroxenes range from +5.23‰ to +5.78‰ and olivines range from +4.83‰ to +5.47‰. Coexisting glass and phenocrysts in the lavas are in isotopic equilibrium, with one exception. Oxygen isotope ratios of back-arc lavas erupted through oceanic crust are indistinguishable from mid-ocean ridge basalts or lavas erupted in nearby back-arc settings. Although lavas from the arc front display elevated oxygen isotope ratios, the magnitude of 18O-enrichment is too great to result from recycling of subducted material alone. A single back-arc lava erupted through continental crust is also relatively 18O-rich suggesting that the most likely origin for the high δ 18O signature is limited amounts of interaction between continental crust and melts derived from a mantle wedge that has been variably fluxed by recycled oxygen. The results of modelling open system behaviour in this volcanic system highlight the need for strong controls on the composition of local contaminants. Application of ‘average' crustal lithologies, as in other volcanic provinces, may lead to erroneous conclusions regarding the involvement of local basement. 相似文献
10.
Gas is extracted from large (6–31 kg) Antarctic ice samples to obtain sufficient CO 2 for 14C measurements with small low-level proportional counters. The 14C ages of Byrd core ice are in accord with glaciological estimates ranging from (2.2 −1.1+1.4)×10 3 yr at 271 m depth to more than 8 × 10 3 yr at 1071 m depth. The CO 2 abundances in gas extracted from Byrd core ice range from 0.0216 to 0.051%, with below present-day atmosphere CO 2 abundances for ice from 1068 and 1469 m depths. The CO 2 abundance in gas from Allan Hills surface ice samples ranges between four and six times the atmospheric value and the CO 2 had a specific activity three times that of contemporary carbon. A possible explanation for the anomalously high specific activity is surface melting with the incorporation into CO 2 of 14C produced by cosmic ray spallation of oxygen in ice. The CO 2 abundance in gas extracted from subsurface Allan Hills ice ranged from 0.030 to 0.065%, and the specific activities are below contemporary carbon, indicating ages greater than 5×10 3 yr. The 18O/ 16O ratio of oxygen in the trapped gas is the same as that of atmospheric oxygen and differs markedly from the 18O/ 16O ratio in the ice. The O 2, N 2, and Ar abundances and isotopic compositions are similar to those in contemporary air, except for positive 15N/ 14N ratios in a few samples. 相似文献
11.
Isotopic variations in melting snow are poorly understood. We made weekly measurements at the Central Sierra Snow Laboratory, California, of snow temperature, density, water equivalent and liquid water volume to examine how physical changes within the snowpack govern meltwater δ18O. Snowpack samples were extracted at 0.1 m intervals from ground level to the top of the snowpack profile between December 1991 and April 1992. Approximately 800 mm of precipitation fell during the study period with δ18O values between −21.35 and −4.25‰. Corresponding snowpack δ18O ranged from −22.25 to −6.25‰. The coefficient of variation of δ18O in snowpack levels decreased from −0.37 to −0.07 from winter to spring, indicating isotopic snowpack homogenization. Meltwater δ18O ranged from −15.30 to −8.05‰, with variations of up to 2.95‰ observed within a single snowmelt episode, highlighting the need for frequent sampling. Early snowmelt originated in the lower snowpack with higher δ18O through ground heat flux and rainfall. After the snowpack became isothermal, infiltrating snowmelt displaced the higher δ18O liquid in the lower snowpack through a piston flow process. Fractionation analysis using a two-component mixing model on the isothermal snowpack indicated that δ18O in the initial and final half of major snowmelt was 1.30‰ lower and 1.45‰ higher, respectively, than the value from simple mixing. Mean snowpack δ18O on individual profiling days showed a steady increase from −15.15 to −12.05‰ due to removal of lower δ18O snowmelt and addition of higher δ18O rainfall. Results suggest that direct sampling of snowmelt and snow cores should be undertaken to quantify tracer input compositions adequately. The snowmelt sequence also suggests that regimes of early lower δ18O and later higher δ18O melt may be modeled and used in catchment tracing studies. 相似文献
12.
This study presents the chronological evolution of the upper amphibolite facies Orue Unit in NW Namibia. Metasedimentary and meta-igneous rocks of the Orue Unit were investigated using the Pb–Pb stepwise leaching technique on garnet and rutile, U–Pb multi-grain analysis on rutile, Sm–Nd–Lu–Hf leaching technique on garnet, SHRIMP analysis on zircon and Ar–Ar dating on amphibole. Each of these techniques pertains to different processes that occurred before, during, or after the metamorphic peak. Our age data can be integrated with petrological constraints to provide a more complete understanding of the metamorphic cycle. Our pre-peak metamorphic zircon ages, peak metamorphic garnet ages and peak to late peak metamorphic amphibole 39Ar– 40Ar ages bracket the upper amphibolite facies metamorphic event including hydration or dehydration processes into a time span of only ca. 20 Ma. The age data obtained by peak metamorphic mineral analyses cluster around 1340–1320 Ma. Based on age data and field observation, we interpret the upper amphibolite facies metamorphism as a large-scale regional mid-crustal event. Spot analyses of inherited zircon cores obtained by SHRIMP reflect the sedimentary origin of the respective rocks of the Orue Unit and derivation from Palaeoproterozoic protoliths. The metamorphic rocks south of the anorthositic Kunene Intrusive Complex (KIC) have previously been ascribed to the Palaeoproterozoic Epupa Complex at the SW margin of the Congo craton and were thus thought to be older than the Mesoproterozoic KIC. Our data show that the high-grade metamorphic overprint took place 30–50 Ma after emplacement of the KIC. Rutile growth ages of 1248 Ma in one sample reflect fluid activity which seems to be a local phenomenon since there is no other evidence of geological activity throughout the Orue Unit at that time. The rutile ages predate the emplacement of satellite intrusions in that area by 30 Ma and there is no causal relation between these two events. 相似文献
13.
基于2517套现场测量资料,245块岩石样品的体积磁化率测量和详细的岩矿鉴定及硅酸盐全分析结果,结合单矿物磁化率特征及各岩石之间的对比研究,发现岩石磁化率主要受组成岩石的矿物磁化率控制.即岩石磁化率(κr)与组成岩石各个矿物磁化率(κ1)及其体积含量(C2)成正比.例如侵入岩磁化率,κr=-5.68×102Cq+2.8... 相似文献
14.
In eastern England the Chalk aquifer is covered by extensive Pleistocene deposits which influence the hydraulic conditions and hydrochemical nature of the underlying aquifer. In this study, the results of geophysical borehole logging of groundwater temperature and electrical conductivity and depth sampling for major ion concentrations and stable isotope compositions (δ 18O and δ 2H) are interpreted to reveal the extent and nature of the effective Chalk aquifer of north Norfolk. It is found that the Chalk aquifer can be divided into an upper region of fresh groundwater, with a Cl concentration of typically less than 100 mg l −1, and a lower region of increasingly saline water. The transition between the two regions is approximately 50 m below sea-level, and results in an effective aquifer thickness of 50–60 m in the west of the area, but less than 25 m where the Eocene London Clay boundary is met in the east of the area. Hydrochemical variations in the effective aquifer are related to different hydraulic conditions developed in the Chalk. Where the Chalk is confined by low-permeability Chalky Boulder Clay, isotopically depleted groundwater (δ 18O less than −7.5‰) is present, in contrast to those areas of unconfined Chalk where glacial deposits are thin or absent (δ 18O about −7.0‰). The isotopically depleted groundwater is evidence for groundwater recharge during the late Pleistocene under conditions when mean surface air temperatures are estimated to have been 4.5°C cooler than at the present day, and suggests long groundwater residence times in the confined aquifer. Elevated molar Mg:Ca ratios of more than 0.2 resulting from progressive rock-water interaction in the confined aquifer also indicate long residence times. A conceptual hydrochemical model for the present situation proposes that isotopically depleted groundwater, occupying areas where confined groundwater dates from the late Pleistocene, is being slowly modified by both diffusion and downward infiltration of modem meteoric water and diffusive mixing from below with an old saline water body. 相似文献
15.
The stable isotopic composition of hydrogen and oxygen ( δ2H and δ18O) and tritium activity ( 3H) were monitored in monthly precipitation at two continental stations (Ljubljana, Zagreb) and six stations along the eastern Adriatic coasts of Slovenia and Croatia in the period 2001–2003. Mean air temperatures and amount of precipitation were also recorded. Distinct differences in both meteorological and isotopic data between the continental and maritime stations were observed. Seasonal variations in δ18O are smaller at the maritime stations than at the continental ones due to smaller seasonal temperature variations. A good correlation between δ18O and δ2H was obtained for each station, and the local meteoric water lines are close to the Global Meteoric Water Line, with a decreasing trend of slope for the south-Adriatic stations. Good correlations between δ18O in monthly precipitation and mean monthly air temperature were observed at all stations. The slope of δ18O vs. T varied between 0.37‰ °C−1 and 0.15‰ °C−1. Mean 3H activity and seasonal variation of 3H activity are smaller at maritime stations than at continental ones. Additionally, 3H activity decreases in the NW–SE direction of the Adriatic coast. The study of spatial variations over this relatively small area rich in geographical and climatic diversities showed the complexity of the isotopic composition of precipitation and the isotopic data obtained for eight stations, most of them in the karstic area along the Adriatic coast, and gave valuable information for regional hydrological investigations and modelling of isotope variability over the Mediterranean basin. 相似文献
16.
High-precision in-situ ion microprobe (SIMS) oxygen isotope analysis of zircons from two diorite intrusions associated with the late Caledonian Lochnagar pluton in Scotland has revealed large differences in the degree of heterogeneity in zircon δ18O between the diorites. Zircon crystals from the Cul nan Gad diorite (CnG) show a unimodal distribution of oxygen isotope values ( δ18O = 6.0 ± 0.6‰ (2 σ)) and no or only minor grain-scale variation. Those from the Allt Darrarie diorite (AD1) show a large range in δ18O and an apparent bimodal distribution with modes of 6.6 ± 0.4‰ and 7.3 ± 0.4‰. Variations of up to 1.2‰ occur between and within grains; both an increase and decrease in δ18O with zircon growth has been observed. The δ18O composition of growing zircon can only change if open-system processes affect the magma composition, i.e. if material of contrasting δ18O composition is added to the magma. The variability in AD1 is interpreted to represent a cryptic record of magma mixing. A ‘deep crustal hot zone’ is a likely site for generation of the dioritic magmas which developed by mixing of residual melts and crustal partial melts or by melting of mafic lower crustal rocks. The overall small number of zircons with mantle-like δ18O values (5.3 ± 0.6‰ (2 σ)) in the Lochnagar diorites is largely the product of crustal differentiation rather than crustal growth. The δ18O of quartz from the CnG and AD1 diorites shows only minor variation (CnG: 10.9 ± 0.5‰ (2σ), AD1: 11.7 ± 0.6‰ (2σ)) within single populations, with no evidence of mixing. Quartz–zircon isotopic disequilibrium is consistent with later crystallisation of quartz from late magmatic fluids, and in case of the AD1 diorite after the inferred magma mixing from a homogenised, higher δ18O melt. High-precision SIMS oxygen isotope analysis of zircon provides a new approach to identifying and resolving previously undetected early-stage magma mixing and constraining the compositions and origins of the component magmas. A combination of zircon, quartz and whole-rock data has proven to be a powerful tool in reconstructing the petrogenetic evolution of diorite from early crystallisation to late alteration. 相似文献
17.
The first comprehensive chemical and Sr–Nd–Pb isotopic data set of Plio–Pleistocene tholeiitic and alkaline volcanic rocks cropping out in Sardinia (Italy) is presented here. These rocks are alkali basalts, hawaiites, basanites, tholeiitic basalts and basaltic andesites, and were divided into two groups with distinct isotopic compositions. The vast majority of lavas have relatively high 87Sr/ 86Sr (0.7043–0.7051), low 143Nd/ 144Nd (0.5124–0.5126), and are characterised by the least radiogenic Pb isotopic composition so far recorded in Italian (and European) Neogene-to-Recent mafic volcanic rocks ( 206Pb/ 204Pb=17.55–18.01) (unradiogenic Pb volcanic rocks, UPV); these rocks crop out in central and northern Sardinia. Lavas of more limited areal extent have chemical and Sr–Nd–Pb isotopic ratios indicative of a markedly different source ( 87Sr/ 86Sr=0.7031–0.7040; 143Nd/ 144Nd=0.5127–0.5129; 206Pb/ 204Pb=18.8–19.4) (radiogenic Pb volcanic rocks, RPV), and crop out only in the southern part of the island. The isotopic ratios of these latter rocks match the values found in the roughly coeval anorogenic (i.e. not related to recent subduction events in space and time) mafic volcanic rocks of Italy (i.e. Mt. Etna, Hyblean Mts., Pantelleria, Linosa), and Cenozoic European volcanic rocks. The mafic rocks of the two Sardinian rock groups also show distinct trace element contents and ratios (e.g. Ba/Nb>14, Ce/Pb=8–25 and Nb/U=29–38 for the UPV; Ba/Nb<9, Ce/Pb=24–28 and Nb/U=46–54 for the RPV). The sources of the UPV could have been stabilised in the Precambrian after low amounts of lower crustal input (about 3%), or later, during the Hercynian Orogeny, after input of Precambrian lower crust in the source region, whereas the sources of the RPV could be related to processes that occurred in the late Palaeozoic–early Mesozoic, possibly via recycling of proto-Tethys oceanic lithosphere by subduction. 相似文献
18.
Measurements of tritium and 18O concentrations in precipitation and runoff were used to provide further insight into the groundwater storage properties of the Wimbachtal Valley, a catchment area of 33.4 km 2, extending between 636 and 2713 m a.s.l. in the Berchtesgaden Alps. The catchment includes three aquifer types: a dominant porous aquifer; a fractured dolomite; a karstic limestone aquifer. Employing a simple hydrological model, information about mean transit times of environmental tracers is derived for the groundwater runoff component and several karst springs from the application of the exponential and dispersion flow models to the isotopic input and output data. The mean transit times calculated from a dispersion model with transit times of 4.1 years for 18O and 4.2 years for tritium, which agree well, allow calculation of total (mobile + stagnant) groundwater storage volume, which is equivalent to 6.6 m of water depth. Direct runoff appears negligible as in many other cases. 相似文献
19.
New U–Pb age-data from zircons separated from a Northland ophiolite gabbro yield a mean 206Pb/ 238U age of 31.6 ± 0.2 Ma, providing support for a recently determined 28.3 ± 0.2 Ma SHRIMP age of an associated plagiogranite and 29–26 Ma 40Ar/ 39Ar ages ( n = 9) of basalts of the ophiolite. Elsewhere, Miocene arc-related calc-alkaline andesite dikes which intrude the ophiolitic rocks contain zircons which yield mean 206Pb/ 238U ages of 20.1 ± 0.2 and 19.8 ± 0.2 Ma. The ophiolite gabbro and the andesites both contain rare inherited zircons ranging from 122–104 Ma. The Early Cretaceous zircons in the arc andesites are interpreted as xenocrysts from the Mt. Camel basement terrane through which magmas of the Northland Miocene arc lavas erupted. The inherited zircons in the ophiolite gabbros suggest that a small fraction of this basement was introduced into the suboceanic mantle by subduction and mixed with mantle melts during ophiolite formation. We postulate that the tholeiitic suite of the ophiolite represents the crustal segment of SSZ lithosphere (SSZL) generated in the southern South Fiji Basin (SFB) at a northeast-dipping subduction zone that was initiated at about 35 Ma. The subduction zone nucleated along a pre-existing transform boundary separating circa 45–20 Ma oceanic lithosphere to the north and west of the Northland Peninsula from nascent back arc basin lithosphere of the SFB. Construction of the SSZL propagated southward along the transform boundary as the SFB continued to unzip to the southeast. After subduction of a large portion of oceanic lithosphere by about 26 Ma and collision of the SSZL with New Zealand, compression between the Australian Plate and the Pacific Plate was taken up along a new southwest-dipping subduction zone behind the SSZL. Renewed volcanism began in the oceanic forearc at 25 Ma producing boninitic-like, SSZ and within-plate alkalic and calc-alkaline rocks. Rocks of these types temporally overlap ophiolite emplacement and subsequent Miocene continental arc construction. 相似文献
20.
Gabbro breccias were recovered from an anomalously shallow level of the ocean crust during DSDP Leg 82. The rocks display evidence of metamorphic crystallization related either to localized deformation or to hydrothermal circulation of a seawater-derived fluid under static conditions. Secondary phases consist of plagioclase, amphibole and minor clinopyroxene, ilmenite, sphene and chlorite. Petrological study indicates that deformation took place at high temperature, under anhydrous conditions, and was followed by hydrothermal circulation. The compositions of secondary minerals (i.e. strong zonations, presence of chlorine in amphiboles, varying compositions of secondary plagioclase) indicate that reactions of the gabbros with the fluids occurred at a low water/rock ratio. Relations between Cl, Na and K in amphiboles suggest penetration of at least two distinct fluids of different compositions. Metamorphic crystallization stopped when greenschist facies conditions were reached( 350°C), probably because hydrothermal circulation faded out. 相似文献
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