Oxygen isotopes and the origin of high-87Sr/86Sr andesites

Andesites from the Peruvian Andes and the Banda arc of Indonesia are characterized by unusually high and variable ⁸⁷Sr/⁸⁶Sr ratios. The Banda arc samples, including two cordierite-bearing lavas from Ambon, show a clear positive correlation between ⁸⁷Sr/⁸⁶Sr and δ¹⁸O. The andesitic rocks have δ¹⁸O values that range from 5.6 to 9.2‰. Over that range in δ¹⁸O, ⁸⁷Sr/⁸⁶Sr increases from 0.7044 to 0.7095. The cordierite-bearing lavas have δ¹⁸O values of approximately 15‰ and ⁸⁷Sr/⁸⁶Sr ratios of approximately 0.717. The similarity between δ¹⁸O values and ⁸⁷Sr/⁸⁶Sr ratios in total rocks and separated plagioclase phenocrysts of the Banda arc samples indicates that the measured isotope ratios are primary and have not been affected by secondary, low-temperature post-eruptive alteration. The observed variation between O and Sr isotopic ratios can be modeled by two-component mixing in which one component is of mantle isotopic composition. As the crust beneath the Banda arc is probably oceanic, contamination of the manle component may have resulted from the subduction of either continentally-derived sediments or continental crust. Mixing calculations indicate that the contaminant could have an isotopic composition similar to that observed in the cordierite-bearing lavas.The Andean samples, despite petrographic evidence of freshness, exhibit whole-rock δ¹⁸O values significantly higher than those of corresponding plagioclase phenocryst separates, indicating extensive low-temperature post-eruptive alteration. The plagioclase mineral separates show a range of δ¹⁸O values between 6.9 and 7.9‰. The ⁸⁷Sr/⁸⁶Sr ratios of these same samples are, in most instances, not significantly different from those measured for the whole rock, thus signifying that the phenocrysts and groundmass were in isotopic equilibrium at the time of eruption. Unlike the lavas of the Banda arc, the Andean lavas show no strong positive correlation between ⁸⁷Sr/⁸⁶Sr ratios and δ¹⁸O values, but instead lower ⁸⁷Sr/⁸⁶Sr ratios appear to be associated with higher δ¹⁸O values. The δ¹⁸O and ⁸⁷Sr/⁸⁶Sr values of the Peruvian samples are both slightly higher than those of “normal” island arc volcanics.The small proportions of contaminant implied by the O isotope results seem to preclude continental crustal contamination as a primary cause of high ⁸⁷Sr/⁸⁶Sr ratios. The most plausible process that can explain both O and Sr isotope results is one in which sediments of continental origin are partially melted in the subduction zone. These melts rise into overlying mantle material and subsequently participate in the formation of calc-alkaline magmas.If the involvement of a sialic component in the genesis of andesitic magma occurs in the subduction zone, melting of that sialic material signifies temperatures of at least 750–800°C at the top of the subducted lithospheric slab at depths of approximately 150 km. The fact that contamination has apparently occurred in the Banda arc samples without producing any simple widespread correlations between Sr and O isotopic compositions on the one hand and major or trace element abundances on the other, shows that isotopic correlations, possibly including pseudo-isochrons, can be produced by mixing without producing trace element mixing correlations. Because O versus Sr isotope correlations are little affected by processes of partial melting of differentiation, they provide a direct means of testing whether Sr isotopic variations in volcanic rocks are of mantle origin or are due instead to mixing with sialic material.     

Multiple‐indicator study of groundwater flow and chemistry and the impacts of river and paddy water on groundwater in the alluvial fan of the Tedori River,Japan

To investigate the source, flow paths, and chemistry of rich resources of high‐quality, shallow groundwater in the alluvial fan between the Tedori and Sai rivers in central Japan, we analysed stable isotope ratios of H, O, and Sr and concentrations of major dissolved ions and trace elements in groundwater, river water, and paddy water. The ⁸⁷Sr/⁸⁶Sr ratios of the groundwater are related to near‐surface geology: groundwater in sediment from the Tedori River has high ⁸⁷Sr/⁸⁶Sr ratios (>0.711), whereas that from the Sai River in the north of the fan has low ⁸⁷Sr/⁸⁶Sr ratios (<0.711). δ²H and δ¹⁸O values and ⁸⁷Sr/⁸⁶Sr ratios indicate that groundwater in the central and southern fans is recharged by the Tedori River, whereas recharge in the north is from the Sai River. Mg²⁺, Ca²⁺, Sr²⁺, HCO₃^?, and SO₄^2? concentrations and δ²H and δ¹⁸O values in the groundwater are high in the central fan and, except for the northern area, tend to increase with distance from the Tedori River. There are linear relationships between ⁸⁷Sr/⁸⁶Sr ratio and the reciprocal concentrations of Sr²⁺, Mg²⁺, and Ca²⁺. These geochemical characteristics suggest that as groundwater recharged from the Tedori River flows towards the central fan, it mixes with waters derived from precipitation and paddy water that have become enriched in these components during downward infiltration. These results are consistent with our hydrological analysis and numerical simulation of groundwater flow, thus verifying the validity of the model we used in our simulation of groundwater flow. Copyright © 2016 John Wiley & Sons, Ltd.     

Strontium and oxygen isotopic composition of some basalts from Hole 504B,Costa Rica Rift,DSDP Legs 69 and 70

Seventeen whole-rock samples, generally taken at 25–50 m intervals from 5 to 560 m sub-basement in Hole 504B, drilled in 6.2 m.y. old crust, were analysed for⁸⁷Sr/⁸⁶Sr ratios, Sr and Rb concentrations, and¹⁸O/¹⁶O ratios. Sr isotope ratios for 8 samples from the upper 260 m of the hole range from 0.70287 to 0.70377, with a mean of 0.70320. In the 330–560 m interval, 5 samples have a restricted range of 0.70255–0.70279, with a mean of 0.70266, the average value for fresh mid-ocean ridge basalts (MORB). In the 260–330 m interval, approximately intermediate Sr isotopic ratios are found.δ¹⁸O values (‰) range from 6.4 to 7.8 in the upper 260 m, 6.2–6.4 in the 270–320 m interval, and 5.8–6.2 in the 320–560 m interval. The values in the upper 260 m are typical for basalts which have undergone low-temperature seawater alteration, whereas the values for the 320–560 m interval correspond to MORB which have experienced essentially no oxygen isotopic alteration.The higher⁸⁷Sr/⁸⁶Sr and¹⁸O/¹⁶O ratios in the upper part of the hole can be interpreted as the result of a greater overall water/rock ratio in the upper part of the Hole 504B crust than in the lower part. Interaction of basalt with seawater(⁸⁷Sr/⁸⁶Sr=0.7091) increased basalt⁸⁷Sr/⁸⁶Sr ratios and produced smectitic alteration products which raised whole-rock δ¹⁸O values. Seawater circulation in the lower basalts may have been partly restricted by the greater number of relatively impermeable massive lava flows below about 230 m sub-basement. These flows may have helped to seal off lower basalts from through-flowing seawater.     

Oxygen isotopic compositions of the late orogenic granites in the Southern Piedmont of the Appalachian Mountains,U.S.A., and their relationship to subcrustal structures and lithologies

Data were acquired from 143 whole rock samples from 20 late orogenic, post-metamorphic, Hercynian-age granitic plutons from the Piedmont of the southern Appalachians, principally in Georgia and South Carolina. These plutons exhibit a regional gradient in oxygen isotopic compositions in which the granites confined to the Inner Piedmont to the northwest are¹⁸O-enriched (11.4 to 7.9) whereas those toward the southeast within the Charlotte-Slate and portions of the Kiokee belts have distinctly lower¹⁸O/¹⁶O compositions (8.2 to 5.5); one body that lies along the southeastern edge of the Piedmont in South Carolina, however, appears to be anomalously¹⁸O-enriched (8.9). Most plutons display¹⁸O/¹⁶O variations of <1‰ although two vary by as much as 3–4‰. The regional oxygen isotopic pattern among plutons appears to correlate directly with: (1) regional Bouguer gravity patterns, in which the¹⁸O-enriched plutons occupy areas characterized by negative anomalies, whereas low-¹⁸O bodies are invariably restricted to regions of positive anomalies; (2)⁸⁷Sr/⁸⁶Sr data, where granites with δ¹⁸O values <8‰ have low initial strontium ratios of ～0.703 to 0.705, while¹⁸O-enriched plutons (>9‰) have ratios >0.710; (3) contrasting chemical and accessory mineral compositions, in which many¹⁸O-depleted granites have a number of I-type characteristics, whereas several of the most¹⁸O-enriched plutons exhibit a number of S-type features. It can be inferred from these data that the¹⁸O-enriched granites were formed from continental crustal protoliths that underlie much of the Inner Piedmont and portions of the Kiokee belt, whereas the low-¹⁸O plutons were derived from more mafic sources beneath the Charlotte-Slate and portions of the Kiokee belt. The overall correspondence between the regional¹⁸O/¹⁶O patterns exhibited by the granites and gravity data implies that these grantes may be essentially rooted to their protoliths, in turn suggesting that the large-scale translational movement recently proposed for the Southern Piedmont may have occurred prior to intrusion of these granites ～320 m.y. ago.     

Strontium isotope geochemistry of late cretaceous granodiorites,Jamaica and Haiti,greater Antilles

Initial⁸⁷Sr/⁸⁶Sr ratios have been determined for a representative suite of Upper Cretaceous granodiorites and associated rocks from the Above Rocks composite stock in central Jamaica and the Terre-Neuve pluton in northwestern Haiti. The average initial⁸⁷Sr/⁸⁶Sr ratio for severn samples of the Terre-Neuve intrusion is 0.7036, with a range of 0.7026–0.7047. For two samples of the Above Rocks the initial ratios are 0.7033 and 0.7034. A third sample from this intrusive has an initial ratio of 0.7084, which is tenatively attributed to contamination. The initial⁸⁷Sr/⁸⁶Sr ratios indicate that neither ancient sialic crust nor sediments carried down a Benioff zone can be the primary source of the granodioritic magma. K/Rb ratios for these rocks range from 178 to 247, which are much lower than the average values (≥1000) for tholeiitic basalts. It is concluded that the magmas originated primarily by melting of downthrust oceanic crust or adjacent mantle material.     

Oxygen isotopic compositions of Central Andean plutonic and volcanic rocks,latitudes 26°–29° south

Oxygen isotope data are reported for 27 igneous rocks of Mesozoic to Quaternary age from the Central Andes. 26–29°S. The plutonic rocks, and most of the volcanics, have δ¹⁸O values between 6.2 and 8.3‰.The whole-rock δ¹⁸O values show a weak correlation with initial⁸⁷Sr/⁸⁶Sr data. This O-Sr array differs from documented trends for calc-alkaline plutonic suites from California, Scotland and northern Italy, but overlaps with data for volcanic and plutonic rocks from Ecuador, northern Chile and southern Perú.The oxygen isotope results indicate that the magmas evolved without significant contamination from supracrustal rocks (e.g., rocks that experienced¹⁸O enrichment during surficial weathering). The available O, Sr and Pb isotopic data for these rocks are best explained by magma generation in the upper mantle or lower crust. From the Late Mesozoic on, the⁸⁷Sr/⁸⁶Sr values were modified at depth by isotopic exchange between the magma and a continually thickening crust of plutonic rocks of Late Precambrian to early Mesozoic age.     

Isotopic geochemistry (O,Sr, Pb) of the Golda Zuelva and Mboutou anorogenic complexes,North Cameroun: mantle origin with evidence for crustal contamination

The annular (6–8 km diameter) Golda Zuelva and Mboutou anorogenic complexes of North Cameroun are composed of a suite of alkaline plutonic rocks ranging from olivine gabbro to amphibole and biotite granite. For the Mboutou complex there are two overlapping centres. In the Golda Zuelva complex the plutonic rocks are associated with a later hawaiite to rhyolite volcanic suite. A Rb/Sr whole rock isochron gives an age of 66±3 Ma for the Golda Zuelva granites, with initial⁸⁷Sr/⁸⁶Sr ratio of 0.7020, and demonstrates that plutonism and volcanism were essentially contemporaneous and probably cogenetic. For Golda Zuelva and the north Mboutou centre¹⁸O/¹⁶O (5.6–6.2),⁸⁷Sr/⁸⁶Sr (0.7030–0.7045) and Pb isotopic ratios (²⁰⁷Pb/²⁰⁴Pb: 15.60–15.64) support a mantle origin for the initial magmas. Unlike Sr isotopes, the O isotopic ratios of the granitic end members at Golda Zuelva (～7.5) indicate crustal contamination. Post-magmatic alteration was not significant.For the younger south Mboutou centre the O-, Sr- and Pb-isotopic data indicate more extensive magma-crust interaction and in a different (higher level?) crustal environment with δ¹⁸O granite=3.3‰,⁸⁷Sr/⁸⁶Sr ratios up to 0.706 and Pb isotopic ratios more markedly displaced from the oceanic volcanic field. The low-¹⁸O granites probably record, at least in part, a magmatic process with subsequent minor post-magmatic alteration effects. The major and trace element systematics between the north and south Mboutou centres are directly comparable. The evolution of the magmas were dominated by fractional crystallisation and progressive crustal contamination processes.     

Geochemical and Sr–Nd–Pb isotopic investigation of Triassic granitoids and basement rocks in the northern Gyeongsang Basin, Korea: Implications for the young basement in the East Asian continental margin

Abstract We present chemical and Sr–Nd–Pb isotopic compositions of three Triassic (226–241 Ma) calc‐alkaline granitoids (the Yeongdeok granite, Yeonghae diorite and Cheongsong granodiorite) and basement rocks in the northern Gyeongsang basin, south‐eastern Korea. These plutons exhibit typical geochemical characteristics of I‐type granitoids generated in a continental magmatic arc. The Yeongdeok and Yeonghae plutons have similar initial Sr, Nd and Pb isotope ratios (⁸⁷Sr/⁸⁶Sr_initial = 0.7041 ~ 0.7050, ?_Nd(t) = 2.3 ~ 4.0, ²⁰⁶Pb/²⁰⁴Pb_feldspar = 18.22 ~ 18.34), but distinct rare earth element patterns, suggesting that the two plutons formed from partial melting of a similar source material at different depths. The Cheongsong pluton has slightly more enriched Sr–Nd–Pb isotopic compositions (⁸⁷Sr/⁸⁶Sr_initial = 0.7047 ~ 0.7065, ?_Nd(t) = 3.9 ~ 2.8, ²⁰⁶Pb/²⁰⁴Pb_feldspar = 18.24 ~ 18.37) than the other two plutons. The Nd model ages of the basement rocks (1.1 ~ 1.4 Ga) are slightly older than those of the plutons (0.6 ~ 1.0 Ga). The initial Sr and Nd isotopic ratios of the plutons can be modeled by the mixing between the mid‐oceanic ridge basalt‐like depleted mantle component and the crustal component represented by basement rocks, which is also supported by Pb isotope data. The Sr and Nd isotope data from granitoids and basement rocks suggest that the Gyeongsang basin, the Hida belt and the inner zone of south‐western Japan share relatively young basement histories (middle Proterozoic), compared with those (early Proterozoic to Archean) of the Gyeonggi and Yeongnam massifs and the Okcheon belt. The Nd isotope data of basement rocks suggest that the Hida belt might be better correlated with the basement of the Gyeongsang basin than the Gyeonggi massif, the Okcheon belt or the Yeongnam massif, although it may represent an older continental margin of East Asia than the Gyeongsang basin considering its slightly older Nd model ages.     

The δ13C–δ18O variations in marble in the Hida Belt,Japan

Marble has a great potential to understand a history of various geological events occurring during tectonic processes. In order to decode metamorphic–metasomatic records on C–O isotope compositions of marble at mid-crustal conditions, we conducted a C–O–Sr isotope study on upper amphibolite-facies marbles and a carbonate–silicate rock from the Hida Belt, which was once a part of the crustal basement of the East Asian continental margin. Carbon and oxygen isotope analyses of calcite from marbles (Kamioka area) and a carbonate–silicate rock (Wadagawa area) show a large variation of δ¹³C [VPDB] and δ¹⁸O [VSMOW] values (from −4.4 to +4.2 ‰ and +1.6 to +20.8 ‰, respectively). The low δ¹³C values of calcites from the carbonate–silicate rock (from −4.4 to −2.9 ‰) can be explained by decarbonation (CO₂ releasing) reactions; carbon–oxygen isotope modeling suggests that a decrease of δ¹³C strongly depends on the amount of silicate reacting with carbonates. The occurrence of metamorphic clinopyroxene in marbles indicates that all samples have been affected by decarbonation reactions. All δ¹⁸O values of calcites are remarkably lower than the marine-carbonate values. The large δ¹⁸O variation can be explained by the isotope exchange via interactions between marble, external fluids, and/or silicates. Remarkably low δ¹⁸O values of marbles that are lower than mantle value (~+5 ‰) suggest the interaction with meteoric water at a later stage. Sr isotope ratios (⁸⁷Sr/⁸⁶Sr = 0.707255–0.708220) might be close to their protolith values. One zircon associated with wollastonite in a marble thin-section yields a U–Pb age of 222 ± 3 Ma, which represents the timing of the recrystallization of marble, triggered by H₂O-rich fluid infiltration at a relatively high-temperature condition. Our isotope study implies that the upper amphibolite-facies condition, like the Hida Belt, might be appropriate to cause decarbonation reactions which can modify original isotope compositions of marble if carbonates react with silicates.     

Early Cretaceous I‐type granites in the southwest Fujian Province: new constraints on the late Mesozoic tectonic evolution of southeast China

Zircons from two samples of the Sukeng pluton in the southwest Fujian Province, China, were analyzed by LA–ICP–MS with the aim of determining the timing of formation. The zircons from the two samples yield similar U–Pb ages of 100.47 ± 0.42 and 102.46 ± 0.69 Ma, indicating that the Sufeng pluton is contemporaneous with the Sifang and Luoboling plutons, all of which are also related to Cu–Au–Pb–Zn–Mo mineralization within the study area. All three plutons have geochemical features of I‐type granites, are high‐ to mid‐K calc‐alkaline metaluminous rocks, and have average molar Al₂O₃/ (CaO+Na₂O+K₂O) values of 0.95, initial ⁸⁷Sr/⁸⁶Sr ratios of 0.70465–0.70841, εNd(t) values at 101 Ma from –1.72 to –7.26, and two‐stage Nd model ages (T_2DM) from 1.16 to 1.60 Ga. Zircons within these plutons have εHf(t) values at 101 Ma from –3.5 to 6.25 and T_2DM ages from 0.74 to 1.46 Ga, suggesting these I‐type granites formed from magmas generated by partial melting of Mesoproterozoic to Neoproterozoic continental crust that mixed with mantle‐derived magmas. The magmatism was associated with thickening of the lower crust caused by collisions between microcontinents in the Cathaysian Block, which were driven by Early Cretaceous subduction of the Pacific Plate.     

Rb–Sr isochron ages of the Cretaceous granitoids in the Ryoke belt, Kinki district, Southwest Japan

Abstract Granitoids are widely distributed in the Ryoke belt and have been divided into four main igneous stages based on their field setting. In this paper, we present Rb–Sr isochron ages for the younger Ryoke granitoids (second stage to fourth stage) in the Kinki district. The Yagyu granite (second stage) gave a Rb–Sr whole‐rock isochron age of 74.6 ± 10.9 Ma with an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.70938 ± 0.00016, and a Rb–Sr mineral isochron age of 71.8 ± 0.1 Ma. The Narukawa granite (second stage) yielded a Rb–Sr mineral isochron age of 79.5 ± 0.4 Ma. A Rb–Sr whole‐rock isochron age of 78.3 ± 3.0 Ma with an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.70764 ± 0.00014 was obtained for the Takijiri adamellite (third stage). The Katsuragi quartzdiorite (fourth stage) gave a Rb–Sr whole‐rock isochron age of 85.1 ± 18.3 Ma (initial ⁸⁷Sr/⁸⁶Sr ratio of 0.70728 ± 0.00006), and mineral isochron ages of 76.9 ± 0.5 Ma and 74.8 ± 0.5 Ma. The Minamikawachi granite (fourth stage) gave a Rb–Sr whole‐rock isochron age of 72.8 ± 2.0 Ma with an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.70891 ± 0.00021. These age data indicate that the igneous activity in younger Ryoke granitoids of Kinki district occurred between 80 and 70 Ma, except for the Katsuragi quartz diorite. The isotopic data on the various igneous stages in Kinki district correspond with the relative timing from field observations. Based on the initial ⁸⁷Sr/⁸⁶Sr ratios, the granitoids of the Ryoke belt in Kinki district are spatially divided into two groups. One is granitoids with initial ⁸⁷Sr/⁸⁶Sr ratio of 0.707–0.708, distributed in the southern part of the Ryoke belt. The other is granitoids with initial ⁸⁷Sr/⁸⁶Sr ratio of 0.708–0.710 distributed in the northern part of the Ryoke belt. The initial ⁸⁷Sr/⁸⁶Sr ratios of granitoids increase with decreasing (becoming younger) Rb–Sr whole‐rock isochron ages.     

A neodymium,strontium, and oxygen isotopic study of the Cretaceous Samail ophiolite and implications for the petrogenesis and seawater-hydrothermal alteration of oceanic crust

In the Samail ophiolite,¹⁴⁷Sm-¹⁴³Nd,⁸⁷Rb-⁸⁷Sr, and¹⁸O/¹⁶O isotopic systems have been used to distinguish between sea-floor hydrothermal alteration and primary magmatic isotopic variations. The Rb-Sr and¹⁸O/¹⁶O isotopic systems clearly exhibit sensitivity to hydrothermal interactions with seawater while the Sm-Nd system appears essentially undisturbed. Internal isochrons have been determined by the¹⁴⁷Sm-¹⁴³Nd method using coexisting plagioclase and pyroxene and give crystallization ages of 130 ± 12m.y. from Ibra and 100 ± 20 m.y. from Wadi Fizh. These ages are interpreted as the time of formation of the Samail oceanic crust and are older than the inferred emplacement age of 65–85 m.y. The initial¹⁴³Nd/¹⁴⁴Nd ratios for a tectonized harzburgite, cumulate gabbros, plagiogranite, sheeted dikes and a basalt have a limited range in ε_Nd of from 7.5 to 8.6 for all lithologies, demonstrating a clear oceanic affinity and supporting earlier interpretations based on geologic observations and geochemistry. The⁸⁷Sr/⁸⁶Sr initial ratios on the same rocks have an extremely large range of from 0.70296 to 0.70650 (ε_Sr = ?19.7 to +30.5) and the δ¹⁸O values vary from 2.6 to 12.7. These large variations are clearly consistent with hydrothermal interaction of seawater with the oceanic crust. A model is presented for the closed system exchange of Sr and O, that in principle illustrates how the Sr isotopic data may be utilized to estimate the water/rock ratio and subsequently used to evaluate the temperature of equilibration between the water and silicates from the¹⁸O/¹⁶O water-rock fractionation.     

Oxygen and strontium isotopic characteristics of calc-alkalic volcanic rocks from the central and western Japan arcs: Evaluation of contribution of crustal components to the magmas

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.     

The effects of assimilation of country rocks by magmas on 18O/16O and 87Sr/86Sr systematics in igneous rocks

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.     

Initial 87Sr/86Sr ratios of plutonic and volcanic rocks of the Central Andes between latitudes 26° and 29° south

Initial⁸⁷Sr/⁸⁶Sr ratios have been determined for 34 plutonic and volcanic rocks covering the entire age span of magmatic events associated with the Andean orogeny between latitudes 26° and 29° south. The igneous rocks, the majority dated by K/Ar mineral techniques, range in age from Lower Jurassic (190 m.y.) to Quaternary (0.89 m.y.). In addition, initial ratios were determined for three granitoid plutons and one metasediment from the pre-Mesozoic basement which underlies the entire Andean orogen in this transect at shallow depth. The compositions vary from basalt to rhyolite, and from quartz diorite to granodiorite or trondjemite, for the extrusives and intrusives, respectively.Mid-Cretaceous to Quaternary rocks exhibit a systematic west to east increase in mean strontium isotope ratio from 0.7022 to 0.7077, whereas the initial ratios of Jurassic plutons vary from 0.7043 to 0.7059, and do not correlate with age.The existence of unusually low initial ratios (e.g. 0.7022, 0.7023) for several Mesozoic plutonic rocks strongly implies a sub-crustal source for at least some of the Andean magmas. The time-dependent post-Jurassic increase in initial ratio is considered to reflect a systematic change in the composition of partial melts generated in response to the progressive subduction of a lithospheric slab. It is suggested that a systematic change in the locus of melting takes place from along or close to the upper surface of the subduction slab into hanging-wall mantle peridotite as subduction continues.     

Helium,oxygen, strontium and neodymium isotopic relationships in Icelandic volcanics

³He/⁴He ratios have been obtained for basaltic, intermediate and acid volcanic glasses from Iceland. Basaltic glasses exhibit a wide range of ³He/⁴He ratios (4 < R/R_a < 24), which is consistent with the previously recorded range for Icelandic geothermal systems. In contrast the glasses with intermediate and acid compositions have ³He/⁴He values close to the atmospheric value (R_a) with the exception of a 13-Ma sample which has R/R_a= 0.07. ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd ratios and δ¹⁸O values are reported for the same samples.³He/⁴He does not correlate with either ⁸⁷Sr/⁸⁶Sr or ¹⁴³Nd/¹⁴⁴Nd ratio and radiogenic components of He, Sr and Nd have apparently been decoupled. Interaction of Icelandic magmas with hydrothermally altered and older Icelandic crust is the preferred explanation for variable and often low δ¹⁸O values. It is suggested that primary ³He/⁴He ratios may have been modified by incorporation of radiogenic helium developed within the Icelandic crust to impose a larger range of ³He/⁴He ratios on the erupted products than was actually inherited from the mantle beneath Iceland. Intermediate and acid samples have all been severely contaminated by atmospheric helium, most probably at very shallow levels within the crust.     

Late Cenozoic alkaline volcanism in the northwestern Caribbean: tectonic setting and Sr isotopic characteristics

A province of alkaline volcanism has developed over the last 10 m.y. in the northwestern part of the Caribbean plate. Most of the volcanism is Quaternary in age and follows an apparent halving of the spreading rate at the Cayman Rise spreading center 2.4 m.y. ago. Intraplate deformation in Central America and the Nicaraguan Rise has produced a series of north-south orientated grabens. This extensional tectonism is associated temporally and spatially with some of the alkaline magmatism. Strontium isotopic ratios of rocks from sixteen of these centers of volcanism enable three separate areas with different isotopic characteristics to be identified. The largest area corresponds to the Nicaraguan Rise and is characterized by low⁸⁷Sr/⁸⁶Sr ratios (0.7026–0.7031). A more concentrated area of alkaline magmatism in northeastern Costa Rica has intermediate⁸⁷Sr/⁸⁶Sr ratios (0.7036–0.7038) which are within the range shown by the adjacent calc-alkaline volcanoes. In central Hispaniola high⁸⁷Sr/⁸⁶Sr ratios (0.7047–0.7063) are found in strongly alkalic rocks and in rocks that are transitional to calc-alkaline in nature. In both Costa Rica and Hispaniola the increased radiogenic strontium may have come from volatile-rich fluids escaping from adjacent subducting slabs of oceanic crust. The isotopic differences between the two areas may be related to the relative longevity and high rate of subduction in Costa Rica compared to Hispaniola. The Costa Rican alkaline rocks overlie a segment of the Cocos plate which is being subducted at a smaller angle (～ 35°) than at the rest of the Central American arc.     

Strontium,lead and oxygen isotopic investigation of the Skaergard intrusion,East Greenland

New Pb, Sr and O isotopic analyses of rocks from the Skaergard intrusion indicate the following: (1) initial⁸⁷Sr/⁸⁶Sr of the gabbroic magma was less than or equal to 0.7041; (2) limited contamination of magma with crustal Sr and Pb may have occurred in a deep reservoir below the presently exposed parts of the intrusion; (3) marked crustal contamination occurred at high level in marginal border group rocks, but these rocks effectively shielded the main magma body from further interaction with country rock gneisses; (4) subsolidus interaction between Skaergard gabbros and hydrothermal fluids modified δ¹⁸O values but had little effect on Sr and perhaps Pb isotopic ratios; (5) late-stage melanogranophyres may be comagmatic with the Skaergard magma, but silicic granophyres are not; (6) silicic granophyres contain large and varied proportions of crustal Sr and Pb; some may be largely anatectic melts derived from the deep crust whereas others may represent mixing of such anatectic melts with late-stage differentiated liquids of the Skaergard intrusion (e.g. Sydtoppen sill).     

Hydrothermal alteration and tectonic evolution of an intermediate- to fast-spreading back-arc oceanic crust: Late Ordovician Solund-Stavfjord ophiolite, western Norway

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.     

A geochemical study of island-arc and back-arc tholeiites from the Scotia Sea

⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios, REE and selected minor and trace elements are presented and compared for present-day volcanic rocks in the Scotia Sea.Tholeiitic basalts from the South Sandwich Islands show widely ranging contents of some lithophile elements, e.g. K₂O (0.09–0.55%) and Rb (1.55–14.2 ppm), but fairly constant Na₂O and Sr. Total REE contents range from about 4–20 times chondritic abundances with significant light-REE depletion and both positive and negative Eu anomalies. The variations in minor and trace element abundances are consistent with low-pressure fractional crystallization of plagioclase and clinopyroxene but only minor amounts of olivine. The⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios of the parental magmas are thought be 0.7038–0.7039 and 0.51301–0.51314 respectively, and indicate derivation of at least some⁸⁷Sr from subducted ocean crust.The back-arc tholeiites in the Scotia Sea have lower⁸⁷Sr/⁸⁶Sr ratios (0.7028–0.7033), similar¹⁴³Nd/¹⁴⁴Nd ratios (0.51305) and are variably light-REE-enriched(Ce_N/Yb_N= 1.0–1.6). Total REE contents are comparable to those of the South Sandwich Islands tholeiites.