Isotope and trace element evidence for late-stage intra-crustal melting in the High Andes

Purico-Chascon is an acid igneous complex less than 1.5 Ma old rising to 5800 m in the North Chilean Andes, and consisting of andesite-dacite cones and dacite domes on an ignimbrite shield. The rocks are subdivided into two groups: those from Chascon appear to exhibit evidence for magma mixing with more basic material now preserved as xenoliths, whereas among those at Purico no xenoliths have been found.⁸⁷Sr/⁸⁶Sr=0.7095?0.7081 at Purico, 0.7079?0.7069 at Chascon, and 0.7061-0.7057 in the xenoliths from the Chascon lavas:¹⁴³Nd/¹⁴⁴Nd=0.51222?0.51236 overall. The Purico lavas are characterised by higher SiO₂, Rb/Sr,⁸⁷Sr/⁸⁶Sr, and REE abundances, and lower Sr/Nd, Sr/Ba and¹⁴³Nd/¹⁴⁴Nd than most Andean igneous suites. There is no indication ofselective crustal contamination of Sr, or any systematic change in isotope ratios during differentiation. Nonetheless the trend of, for example, high Sr/Nd and Sr contents in rocks with low⁸⁷Sr/⁸⁶Sr (0.704, Ecuador) to low Sr/Nd and Sr and high SiO₂ in rocks with⁸⁷Sr/⁸⁶Sr=0.7081?0.7095 at Purico is interpreted as a shift from subduction zone related magmatism to one with greater crustal affinity. The formation of the least evolved Purico lavas (～60%SiO₂) is discussed in terms of bulk assimilation of crustal material, mixing between crustal- and mantle-derived magmas, and partial melting of pre-existing crust. Although such models are still extremely primitive, the simplest explanation of the observed chemical variations is that the Purico rocks evolved from parental magmas derived by crustal anatexies. Thermal considerations suggest that such late-stage crustal anatexis is a predictable response to crustal thickening which in the Andes is thought to have taken place during the Cenozoic.     

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.     

Origin of the Deccan Trap flows at Mahabaleshwar inferred from Nd and Sr isotopic and chemical evidence

The Deccan flows at Mahabaleshwar are divisible into a lower and an upper group, based on Nd and Sr isotopic ratios, which define two correlated trends. This distinction is supported by incompatible element ratios and bulk compositions. The data reflect contamination in a dynamic system of magmas from an LIL-depleted,ε_JUV ≥ +8 mantle by two different negative ε_JUV endmembers, one undoubtedly continental crust, the other either continental crust or enriched mantle. The depleted mantle source, anomalously high in (⁸⁷Sr/⁸⁶Sr), may have been in the subcontinental lithosphere or a region of rising Indian Ocean MORB mantle.     

Sr–Nd isotope ratios of gabbroic and dioritic rocks in a Cretaceous-Paleogene granite terrain, Southwest Japan

Abstract Whole‐rock chemical and Sr and Nd isotope data are presented for gabbroic and dioritic rocks from a Cretaceous‐Paleogene granitic terrain in Southwest Japan. Age data indicate that they were emplaced in the late Cretaceous during the early stages of a voluminous intermediate‐felsic magmatic episode in Southwest Japan. Although these gabbroic and dioritic rocks have similar major and trace element chemistry, they show regional variations in terms of initial Sr and Nd isotope ratios. Samples from the South Zone have high initial ⁸⁷Sr/⁸⁶Sr (0.7063–0.7076) and low initial Nd isotope ratios (?_Nd, ?2.5 to ?5.3); whereas those from the North Zone have lower initial ⁸⁷Sr/⁸⁶Sr (usually less than 0.7060) and higher Nd isotope ratios (?_Nd, ?0.8 to + 3.3). Regional variations in Sr and Nd isotope ratios are similar to those observed in granitic rocks, although gabbroic and dioritic rocks tend to have slightly lower Sr and higher Nd isotope ratios than granitic rocks in the respective zones. Limited variations in Sr and Nd isotope ratios among samples from individual zones may be attributed partly to a combination of upper crustal contamination and heterogeneity of the magma source. Contamination of magmas by upper crustal material cannot, however, explain the observed Sr and Nd isotope variations between samples from the North and South Zones. Between‐zone variations would reflect geochemical difference in magma sources. The gabbroic and dioritic rocks are enriched in large ion lithophile elements (LILE) and depleted in high field strength elements (HFSE), showing similar normal‐type mid‐ocean ridge basalt (N‐MORB) normalized patterns to arc magmas. Geochronological and isotopic data may suggest that some gabbroic and dioritic rocks are genetically related to high magnesian andesite. Alternatively, mantle‐derived mafic or intermediate rocks which were underplated beneath the crust may be also plausible sources for gabbroic and dioritic rocks. The magma sources (the mantle wedge and lower crust) were isotopically more enriched beneath the South Zone than the North Zone during the Cretaceous‐Paleogene. Sr and Nd isotope ratios of the lower crustal source of the granitic rocks was isotopically affected by mantle‐derived magmas, resulting in similar initial Sr and Nd isotope ratios for gabbroic, dioritic and granitic rocks in each zone.     

Petrogenesis of the Mesozoic intrusive rocks in the Tongling area,Anhui Province,China and their constraint on geodynamic process

TheTonglingarea,whichiscalledtheChineseCopperCapital,isoneofthemostimportantnon-ferrousmetalproducersinChina(e.g.Cu,AuandAg,especiallyCu).ManyresearchershavenotedthatthemetaldepositsarecloselyrelatedtotheMesozoicintrusiverocksinthisarea.Therefore,theTongl…     

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.     

Petrology and isotope-geochemistry of San Vincenzo rhyolites (Tuscany,Italy)

Two groups of rhyolites have been recognized at San Vincenzo (Tuscany, Italy). Group A rhyolites are characterized by plagioclase, quartz, biotite, sanidine and cordierite mineral assemblages. They show constant MgO and variable CaO and Na₂O contents. Initial⁸⁷Sr/⁸⁶Sr ratios in group A samples range between 0.71950 and 0.72535, whereas the Nd isotopic compositions are relatively constant (0.51215–0.51222). Group B rhyolites are characterized by orthopyroxene and clinopyroxene as additional minerals, and show textural, mineralogical and chemical evidence of interaction with more mafic magmas. The Sr and Nd isotopic ratios range between 0.71283–0.71542 and 0.51224–0.51227 respectively. Magmatic inclusions of variable size (1 mm to 10 cm) were found in groups B rhyolites. These inclusions consist mainly of diopsidic clinopyroxene and minor olivine and biotite. They are latitic in composition and represent blobs of hybrid intermediate magmas entrained in the rhyolitic melts. These magmatic inclusions have relatively high Sr contents (996–1529 ppm) and Sr and Nd isotope-ratios of 0.70807–0.70830 and 0.51245–0.51252 respectively.⁸⁷Sr/⁸⁷Sr data on minerals separated from both group A and B rhyolites and magmatic inclusions reveal strong isotopic disequilibria due to the presence of both restitic and newly crystallized phases in group A rhyolites and due to interaction of rhyolites with a mantle-de-rived magma in group B rhyolites. Isotopic data on whole rocks and minerals allow us to interpret the group A rhyolites as representative of different degrees of melting of an isotopically fairly homogeneous pelitic source; conversely, group B rhyolites underwent interactions with a mantle-derived magma. The crustal source as inferred from isotopic systematics would be characterized by⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios close to 0.7194 and 0.51216 respectively. The sub-crustal magma would have Sr isotopic composition close to 0.7077 and a¹⁴³Nd/¹⁴⁴Nd ratio greater than or equal to 0.51252. These isotopic features are different from those reported for the parental magmas postulated for Vulsini and Alban Hills in the nearby Roman Magmatic Province, and are similar to those of the Vesuvius and Ischia magmas.     

Sr–Nd isotopic and chemical characteristics of the silicic magma reservoir of the Aira pyroclastic eruption, southern Kyushu, Japan

Sr and Nd isotope and geochemical investigations were performed on a remarkably homogeneous, high-silica rhyolite magma reservoir of the Aira pyroclastic eruption (22,000 years ago), southern Kyushu, Japan. The Aira caldera was formed by this eruption with four flow units (Osumi pumice fall, Tsumaya pryoclastic flow, Kamewarizaka breccia and Ito pyroclastic flow). Quite narrow chemical compositions (e.g., 74.0–76.5 wt% of SiO₂) and Sr and Nd isotopic values (⁸⁷Sr/⁸⁶Sr=0.70584–0.70599 and _Nd=−5.62 to −4.10) were detected for silicic pumices from the four units, with the exception of minor amounts of dark pumices in the units. The high Sr isotope ratios (0.7065–0.7076) for the dark pumices clearly suggest a different origin from the silicic pumices. Andesite to basalt lavas in pre-caldera (0.37–0.93 Ma) and post-caldera (historical) eruptions show lower ⁸⁷Sr/⁸⁶Sr (0.70465–0.70540) and higher _Nd (−1.03 to +0.96) values than those of the Aira silicic and dark pumices. Both andesites of pre- and post-caldera stages are very similar in major- and trace-element characteristics and isotope ratios, suggesting that the both andesites had a same source and experienced the same process of magma generation (magma mixing between basaltic and dacitic magmas). Elemental and isotopic signatures deny direct genetic relationships between the Aira pumices and pre- and post-caldera lavas. Relatively upper levels of crust (middle–upper crust) are assumed to have been involved for magma generation for the Aira silicic and dark pumices. The Aira silicic magma was derived by partial melting of a separate crust which had homogeneous chemistry and limited isotope compositions, while the magma for the Aira dark pumice was generated by AFC mixing process between the basement sedimentary rocks and basaltic parental magma, or by partial melting of crustal materials which underlay the basement sediments. The silicic magma did not occupy an upper part of a large magma body with strong compositional zonation, but formed an independent magma body within the crust. The input and mixing of the magma for dark pumices to the base of the Aira silicic magma reservoir might trigger the eruptions in the upper part of the magma body and could produce a slight Sr isotope gradient in the reservoir. An extremely high thermal structure within the crust, which was caused by the uprise and accumulation of the basaltic magma, is presumed to have formed the large volume of silicic magma of the Aira stage.     

Postcollisional mantle-derived magmatism, underplating and implications for basement of the Junggar Basin

The late Paleozoic postcollisional granitoids, mafic-ultramafic complexes, and volcanic rocks are extensively distributed around the Junggar Basin; they are generally characterized by positive ε_Nd(t) values, implying that the magmas were mantle-derived and contaminated with crustal materials to some extents. The emplacement of mantle-derived magmas and their differentiates in the upper crust is the expression of deep geological processes at shallow level, while much more mantle-derived magmas were underplated in the lower crust and the region near the crust-mantle boundary, being component part of basement of the Junggar Basin. The postcollisional mafic-ultramafic complexes would not be generated by re-melting of residual oceanic crust, which was considered as the basement of the Junggar Basin, unless very high degrees of partial melting occurred. Even if old continental crust had been present before collision, it would have been strongly modified by the mantle-derived magma underplating. This interpretation is compatible with the existing geophysical data. Project supported by the National Natural Science Foundation of China (Grants Nos. 4900031 and 49272103)     

Rb–Sr and Sm–Nd isotopic studies of mafic igneous rocks from the Ryoke plutono-metamorphic belt in the Setouchi area, Southwest Japan: implications for the genesis and thermal history

Abstract Rb–Sr and Sm–Nd isochron ages were determined for whole rocks and mineral separates of hornblende‐gabbros and related metadiabases and quartz‐diorite from Shodoshima, Awashima and Kajishima islands in the Ryoke plutono‐metamorphic belt of the Setouchi area, Southwest Japan. The Rb–Sr and Sm–Nd whole‐rock‐mineral isochron ages for six samples range from 75 to 110 Ma and 200–220 Ma, respectively. The former ages are comparable with the Rb–Sr whole‐rock isochron ages reported from neighboring Ryoke granitic rocks and are thus due to thermal metamorphism caused by the granitic intrusions. On the contrary, the older ages suggest the time of formation of the gabbroic and related rocks. The initial ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios of the gabbroic rocks (0.7070–0.7078 and 0.51217–0.51231 at 210 Ma, respectively) are comparable with those of neighboring late Cretaceous granites and lower crustal granulite xenoliths from Cenozoic andesites in this region. Because the gabbroic rocks are considered to be fragments of the lower crustal materials interlayered in the granulitic lower crust, their isotopic signature has been inherited from an enriched mantle source or, less likely, acquired through interaction with the lower crustal materials. The Sr and Nd isotopic and petrologic evidence leads to a plausible conclusion that the gabbroic rocks have formed as cumulates from hydrous mafic magmas of light rare earth element‐rich (Sm/Nd < 0.233) and enriched isotopic (?_Sr > 0 and ?_Nd < 0) signature, which possibly generated around 220–200 Ma by partial melting of an upper mantle. We further conclude that they are fragments of refractory material from the lower crust caught up as xenoblocks by granitic magmas, the latter having been generated by partial melting of granulitic lower crustal material around 100 Ma.     

Isotope characteristics of submarine lavas from the Philippine Sea: implications for the origin of arc and basin magmas of the Philippine tectonic plate

Igneous rocks from the Philippine tectonic plate recovered on Deep Sea Drilling Project Legs 31, 58 and 59 have been analyzed for Sr, Nd and Pb isotope ratios. Samples include rocks from the West Philippine Basin, Daito Basin and Benham Rise (40–60 m.y.), the Palau-Kyushu Ridge (29–44 m.y.) and the Parece Vela and Shikoku basins (17–30 m.y.). Samples from the West Philippine, Parece Vela and Shikoku basins are MORB (mid-ocean ridge basalt)-like with ⁸⁷Sr/⁸⁶Sr= 0.7026−0.7032, ¹⁴³Nd/¹⁴⁴Nd= 0.51300−0.51315, and ²⁰⁶Pb/²⁰⁴Pb= 17.8−18.1. Samples from the Daito Basin and Benham Rise are OIB (oceanic island basalt)-like with ⁸⁷Sr/⁸⁶Sr= 0.7038−0.7040, ¹⁴³Nd/¹⁴⁴Nd= 0.51285−0.51291 and ²⁰⁶Pb/²⁰⁴Pb= 18.8−19.2. All of these rocks have elevated ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb compared to the Northern Hemisphere Regression Line (NHRL) and have δ²⁰⁷Pb values of 0 to +6 and δ²⁰⁸Pb values of +32 to +65. Lavas from the Palau-Kyushu Ridge, a remnant island arc, have ⁸⁷Sr/⁸⁶Sr= 7032−0.7035, ¹⁴³Nd/¹⁴⁴Nd= 0.51308−0.51310 and ²⁰⁶Pb/²⁰⁴Pb= 18.4−18.5. Unlike the basin magmas erupted before and after them, these lavas plot along the NHRL and have Pb-isotope ratios similar to modern Pacific plate MORB's. This characteristic is shared by other Palau-Kyushu Arc volcanic rocks that have been sampled from submerged and subaerial portions of the Mariana fore-arc.At least four geochemically distinct magma sources are required for these Philippine plate magmas. The basin magmas tap Source 1, a MORB-mantle source that was contaminated by EMI (enriched mantle component 1 [31]) and Source 2, an OIB-like mantle source with some characteristics of EMII (enriched mantle component 2 [31]). The arc lavas are derived from Source 3, a MORB-source or residue mantle including Sr and Pb from the subducted oceanic crust, and Source 4, MORB-source or residue mantle including a component with characteristics of HIMU (mantle component with high U/Pb [31]). These same sources can account for many of the isotopic characteristics of recent Philippine plate arc and basin lavas. The enriched components in these sources which are associated with the DUPAL anomaly were probably introduced into the asthenosphere from the deep mantle when the Philippine plate was located in the Southern Hemisphere 60 m.y.b.p.     

Lower crustal melting via magma underplating: Elemental and Sr–Nd–Pb isotopic constraints from late Mesozoic intermediate–felsic volcanic rocks in the northeastern North China Block

Ar–Ar dating, major and trace element analyses, and Sr–Nd–Pb isotope results of two groups of Lower Cretaceous (erupted at 126 and 119 Ma, respectively) intermediate–felsic lava from the northeastern North China Block (NCB) suggest their derivation from melting of mixtures between the heterogeneous lower crust and underplated basalts. Both groups exhibit high‐K calc‐alkaline to shoshonitic affinities, characterized by light rare earth element (LREE) and large ion lithophile element (LILE) enrichment and variable high field strength element (HFSE, e.g. Nb, Ta and Ti) depletion, and moderately radiogenic Sr and unradiogenic Nd and Pb isotopic compositions. Compared with Group 2, Group 1 rocks have relatively higher K₂O and Al₂O₃/(CaO + K₂O + Na₂O) in molar ratio, higher HFSE concentrations and lower Nb/Ta ratios, and higher Sr–Nd–Pb isotope ratios. Group 1 rocks were derived from a mixture of an enriched mantle‐derived magma and a lower crust that has developed radiogenic Sr and unradiogenic Nd and Pb isotopic compositions, whereas the Group 2 magmas were melts of another mixture between the same mantle‐derived component and another type of lower crust having even lower Sr, Nd, and Pb isotopic ratios. Shift in source region from Group 1 to Group 2 coincided with a change in melting conditions: hydrous melting of both the underplated basalt and the lower crust produced the earlier high‐Nb and low‐Nb/Ta melts with little or no residual Ti‐rich phases; while the younger low‐Nb and high‐Nb/Ta magmas were melted under a water‐deficient system, in which Ti‐rich phases were retained in the source. Generation of the two groups of intermediate–felsic volcanic rocks was genetically linked with the contemporaneous magma underplating event as a result of lithospheric thinning in the eastern NCB.     

Crustal accretion in the Pan African: Nd and Sr isotope evidence from the Arabian Shield

Nd and Sr isotope determinations on late Precambrian to early Palaeozoic igneous and sedimentary rocks from the Arabian Shield are used to investigate the proportion of reworked “older” crust, and the rate at which new crust was generated during the Pan African event. Eight Rb/Sr whole rock isochrons on igneous suites yield ages in the range 770?590 Ma and initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7038?0.7023. These data confirm that magmatism in this area was largely restricted to the period 850-550 Ma, and the initial ratios are sufficiently low to preclude significant contributions from a long-lived upper crustal source. The initial ¹⁴³Nd/¹⁴⁴Nd ratios of a variety of lithologies, including several samples of possible “basement”, are all higher than the contemporaneous values for CHUR (ε_Nd = +1.6 to +6.9), suggesting that many were derived directly from the upper mantle, and that any inferred crustal source regions for the remainder could not have separated from likely LREE-depleted mantle reservoirs before 1200 Ma. The Arabian Shield therefore provides an example of rapid crustal growth during the Late Proterozoic, and contrasts with the Damara intracratonic belt of Namibia where Nd and Sr isotopes provide strong evidence for extensive reworking of older continental crust during the same period.     

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.     

Implications of correlated Nd and Sr isotopic variations for the chemical evolution of the crust and mantle

Published data showing a linear correlation between initial Nd and Sr isotope compositions in young basalts indicate the existence of a spectrum of isotopically distinct reservoirs in the mantle which represent either (1) mixtures of two homogeneous endmember reservoirs, one of which may be undifferentiated material or (2) fractionated reservoirs all derived from a homogeneous initial reservoir with the same ratio of enrichment factors for Sm/Nd and Rb/Sr. The slope of the correlation, which can be described approximately by (⁸⁷Sr/⁸⁶Sr) = ?3.74114 (¹⁴³Nd/¹⁴⁴Nd) + 2.61935orε_Nd = ?2.7 ε_Sr, places constraints on the origin of these reservoirs and hence on the chemical evolution of the crust-mantle system. The reservoirs could be residual regions of the mantle left after ancient partial melting events. If so, the requirement of constant relative fractionation of Sm/Nd and Rb/Sr in refractory residues is a strong constraint on partial melting models. Calculations suggest that batch melting models are more compatible with this constraint than are fractional melting models, but models incorporating currently accepted distribution coefficients and residual phase assemblages cannot reproduce the observed isotope effects except under highly specific conditions. The slope of the correlation is not consistent with the hypotheses that chemical structure in the mantle is due to accretional heterogeneity or variable loss of elements to the core. If the mantle reservoirs are complementary in composition to the continental crust, and if the crust + mantle has ε_Nd = 0andε_Sr = 0 and chondritic Sr/Nd, then Rb/Sr in the crust is calculated to be less than 0.10, suggesting that the crust may be more mafic in composition and contain a smaller proportion of the earth's Rb and heat-producing elements than previously estimated.     

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.     

Strontium isotope evidence for crustal contamination of calc-alkaline volcanic rocks from Cerro Galan,northwest Argentina

The Pampean Ranges of northwest Argentina are a basin-and-range tectonic province with a late Precambrian to Paleozoic basement and extensive Miocene-Recent calc-alkaline volcanism. The volcanoes include the large resurgent Cerro Galan caldera, and Recent scoria cones and lava flows. Miocene-Recent volcanic rocks of basalt to dacite composition from the Cerro Galan area exhibit a range of Rb/Sr ratios of 0.043–1.092 and initial⁸⁷Sr/⁸⁶Sr ratios of 0.7057–0.7115 with a clear positive correlation between⁸⁷Sr/⁸⁶Sr and⁸⁷Rb/⁸⁶Sr, indicating an apparent age of ca. 130 Ma. This relationship is interpreted to indicate that the Sr isotope variation in the Cerro Galan volcanic rocks results from mixing of a mantle-derived component with low⁸⁷Sr/⁸⁶Sr (<0.7057) and high Sr (>700 ppm) with a crustal component characterized by higher⁸⁷Sr/⁸⁶Sr (>0.7115) and lower Sr (<240 ppm). It is concluded that the mixing is best explained as a result of a small degree of selective crustal Sr contamination (ca. 10%) of a range of subsequently erupted magmas produced largely by fractional crystallization within the continental crust. We propose that the mantle-derived end-member is derived by partial melting of sub-Andean mantle with an⁸⁷Sr/⁸⁶Sr ratio of ca. 0.704, and that such an Sr isotope ratio characterizes the source region for calc-alkaline volcanic rocks throughout the Andes.     

Possible origin of K-rich volcanic rocks from Virunga,East Africa,by metasomatism of continental crustal material: Pb,Nd and Sr isotopic evidence

The isotopic compositions of Sr, Nd and Pb together with the abundances of Rb, Sr, U and Pb have been determined for mafic and felsic potassic alkaline rocks from the young Virunga volcanic field in the western branch of the East African rift system.⁸⁷Sr/⁸⁶Sr varies from 0.7055 to 0.7082 in the mafic rocks and from 0.7073 to 0.7103 in the felsic rocks. The latter all come from one volcano, Sabinyo. Sabinyo rocks have negative ε_Ndvalues ofε_Nd = ?10. Nd and Sr isotopic variations in the basic potassic rocks are correlated and plot between Sabinyo and previously reported [1] compositions (ε_Nd = +2.5;⁸⁷Sr/⁸⁶Sr≈ 0.7047) for Nyiragongo nephelinites. The Pb isotopic compositions for Sabinyo rocks are nearly uniform and average²⁰⁶Pb/²⁰⁴Pb≈ 19.4,²⁰⁷Pb/²⁰⁴Pb= 15.79–15.84,²⁰⁸Pb/²⁰⁴Pb≈ 41.2. The basic potassic rocks have similar²⁰⁶Pb/²⁰⁴Pb values but range in²⁰⁷Pb/²⁰⁴Pb and²⁰⁸Pb/²⁰⁴Pb from the Sabinyo values to less radiogenic compositions.Excellent correlations of⁸⁷Sr/⁸⁶Sr with Rb/Sr, 1/Sr and²⁰⁷Pb/²⁰⁶Pb for Sabinyo rocks suggest these to be members of a hybrid magma series. However, the nearly uniform Pb compositions for this series points to radiogenic growth of⁸⁷Sr in the magma source region following an event which homogenized the isotopic compositions but not Rb/Sr. The Rb-Sr age derived from the erupted Sabinyo isochron-mixing line is consistent with the ～500 Myr Pb-Pb age from Nyiragongo [1], which suggests that this event affected all Virunga magma sources. The event can again be traced in the Pb-Pb, Pb-Sr and Nd-Sr isotopic correlations for all Virunga rocks, including Nyiragongo, when allowances are made for radiogenic growth subsequent to this mixing or incomplete homogenization event. Inferred parent/daughter element fractionations point to a metasomatic event during which a mantle fluid invaded two lithospheric reservoirs: a +ε_Nd reservoir sampled by the Nyiragongo nephelinites and suggested to be the subcontinental mantle and a ?ε_Nd reservoir sampled by the mafic and felsic potasssic volcanism. Whether this ?ε_Nd reservoir is the crust, continental crustal material in the mantle or anomalous mantle cannot be decided from the data. The simplest answer, that this reservoir is the continental crust, seems to be at variance with experimental evidence suggesting a subcrustal origin for basic potassic magmas. Partial melting of the ancient metasomatised lithospheric domains and ensuing volcanism seems to be entirely a response to decompression and rising geotherms during rifting and thinning of the lithosphere.     

Compositional characteristics and geodynamic significance of late Miocene volcanic rocks associated with the Chah Zard epithermal gold–silver deposit,southwest Yazd,Iran

Whole‐rock geochemical and Sr–Nd isotopic data are presented for late Miocene volcanic rocks associated with the Chah Zard epithermal Au–Ag deposit in the Urumieh‐Dokhtar Magmatic Arc (UDMA), Iran, to investigate the magma source, petrogenesis and the geodynamic evolution of the study area. The Chah Zard andesitic to rhyolitic volcanic rocks are characterized by significant Large Ion Lithophile Element (LILE) and Light Rare Earth Element (LREE) enrichment coupled with High Field Strength Element (HFSE) depletion. Our geochemical data indicate an adakitic‐like signature for the volcanic rocks (e.g. SiO₂ > 62 wt%, Al₂O₃ > 15 wt%, MgO < 1.5 wt%, Sr/Y > 70, La/Yb > 35, Yb < 1 ppm, and Y < 18 ppm, and no significant Eu anomalies), distinguishing them from the other volcanic rocks of the UDMA. The Chah Zard volcanic rocks have similar Sr and Nd isotopic compositions; the ⁸⁷Sr/⁸⁶Sr(i) ratios range from 0.704 902 to 0.705 093 and the ε_Nd(i) values are from +2.33 to +2.70. However, the rhyolite porphyry represents the final stage of magmatism in the area and has a relatively high ⁸⁷Sr/⁸⁶Sr ratio (0.705 811). Our data suggest that the andesitic magmas are from a heterogeneous source and likely to result from partial melting of a metasomatized mantle wedge associated with a mixture of subducted oceanic crust and sediment. These melts subsequently underwent fractional crystallization along with minor amounts of crustal assimilation. Our study is consistent with the model that the volcanic host rocks to epithermal gold mineralization in the UDMA are genetically related to late Miocene Neo‐Tethyan slab break‐off beneath Central Iran.