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.     

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.     

Inherited isotope systems and the source region pre-history of early Caledonian granites in the Dalradian Series of Scotland

RbSr and UPb isotope analyses are reported for two pre-metamorphic Caledonian granites which intrude Dalradian rocks in the Central Highlands of Scotland. These data indicate that the origin of the granitic magmas involved partial fusion of old crustal material.UPb systems of zircon size and magnetic fractions from the Ben Vuirich granite are strongly discordant. However, U/Pb isotopic ratios precisely define a chord which intersects concordia at 514_?7⁺⁶ m.y. and 1316_?25⁺²⁶ m.y. Geological constraints suggest that the lower intersection records the post-F₂, pre-M₃ emplacement age of the granite. The upper intersection reflects the presence of old zircon xenocrysts incorporated into the granite magma without complete isotopic resetting. The ultimate source of these xenocrysts is probably a metamorphic basement complex which formed about 1320 m.y. ago, but the immediate source region of the granites could have been Dalradian sediments derived therefrom.RbSr whole-rock systems of the Ben Vuirich granite are also strongly discordant, although 8 out of 13 data points scatter about an “errorchron” of 564 ± 24 m.y. with an initial⁸⁷Sr/⁸⁶Sr ratio of about 0.716. This is interpreted as a spurious result due to incomplete homogenization of Sr isotopes in the source region during partial fusion. Initial⁸⁷Sr/⁸⁶Sr ratios at the time of emplacement indicated by the zircon data ranged from 0.7173 to 0.7191. Whole-rock samples from the Dunfallandy Hill granite have Rb/Sr ratios 2–3 times higher than those from Ben Vuirich and define a reasonably good isochron age of 491 ± 15 m.y. with an initial⁸⁷Sr/⁸⁶Sr of 0.7185 ± 0.0008. This may date granite emplacement or subsequent resetting of the high Rb/Sr rocks during Caledonian metamorphism. RbSr systematics indicate that the crustal source regions of these and other Caledonian granites separated from the upper mantle at least ca. 800 m.y. ago and probably ca. 1300 m.y. ago, thus confirming the interpretation of the upper intersection age of the zircon UPb data.     

Isotopic composition of lead and strontium in lavas and coarse-grained blocks from Ascension Island,South Atlantic

New Sr and Pb isotope data are presented for a selection of lavas and associated coarse-grained blocks from Ascension Island. K-Ar dates for the lavas range up to1.5±0.2Ma. Initial⁸⁷Sr/⁸⁶Sr ratios are consistent with earlier measurements and for most rocks are ca. 0.7029, but range up to 0.7135 in the case of the most evolved lavas and blocks. Pb isotope data are also consistent with earlier measurements, but the Pb in two gabbroic blocks is less radiogenic than Pb in the other rocks. It is suggested that these gabbroic blocks crystallized from a magma of tholeiitic composition whose source was similar to that of mid-oceanic ridge basalt whereas the lavas and other blocks crystallized from mildly alkaline magmas derived from a source further from the crest of the Mid-Atlantic Ridge. The high⁸⁷Sr/⁸⁶Sr ratios result from contamination of the most silicic magma by radiogenic Sr from pelagic sediments. These data and their interpretation are consistent with the petrological and geochemical observations that the granite blocks are the coarse-grained equivalents of the volcanic suite [11] and not fragments of relict continental material [2,3].     

The La Breña — El Jagüey Maar Complex,Durango, Mexico: II. Petrology and geochemistry

A suite of 16 basanitic volcanic rocks, representing all stages in the evolution of the La Breña — El Jagüey (LBEJ) Maar Complex, has been studied petrographically and analyzed for mineral compositions and whole-rock major element, trace element, and Sr–Nd–Pb isotopic compositions. Two feldspathic granulite xenoliths were also studied as possible lower-crustal contaminants to the LBEJ magmas. The volcanic rocks contain the stable minerals olivine, plagioclase, augite, and titanomagnetite±ilmenite, plus a diverse suite of xenocrusts derived from disaggregation of mantle xenoliths of spinel lherzolite (olivine, orthopyroxene, spinel) and lower-crustal granulite xenoliths (plagioclase, quartz, augite, ilmenite). Late-stage interstitial melts rich in Fe and Ti migrated into vesicles in several samples, forming coarse-grained segregation vesicles that are dominated by ilmenite blades up to 2 mm long. The whole-rock elemental data are typical of intra-plate basanitic rocks, with strong enrichments in large ion lithophile elements (i.e. K, Th, U) as well as high field strength elements (i.e. Nb, Ta) relative to mid-ocean ridge basalts (MORB) and estimates of primordial mantle abundances. Mg# increased systematically with time during the evolution of the LBEJ Maar Complex, from 57.0–58.2 in the pre-maar lavas to 59.1–63.8 in the post-maar lavas. Compatible elements (Ca, Sc, Cr, Co, Ni) correlate positively with Mg#, whereas a large group of incompatible elements (Al, Na, K, P, Rb, Sr, Zr, Nb, Ba, La, Ce, Sm, Hf, Ta, Th, U) correlate negatively with Mg#. These trends can be closely reproduced by simple models of fractional crystallization, provided that the incompatible element abundances of the parental, high-Mg# magmas are allowed minor variability. All successful fractionation models demand an important role for augite, despite its presence in the LBEJ volcanic rocks as only a late-stage microphenocrystic and groundmass mineral. Minor garnet fractionation is necessary to produce depletion of heavy rare earth element (REE) abundances in the pre-maar lavas, whose REE patterns cross those for the rest of the suite. The importance of augite and garnet fractionation indicate that the differentiation of the LBEJ magmas took place within the upper mantle, a conclusion that is supported by the presence of spinel lherzolite xenoliths in magmas from all stages in the evolution of the maar complex. Isotopic data for seven LBEJ volcanic rocks show the following ranges: ⁸⁷Sr/⁸⁶Sr 0.70327–0.70347, ^Nd 4.2–5.0, ²⁰⁶Pb/²⁰⁴Pb 18.60–18.81, ²⁰⁷Pb/²⁰⁴Pb 15.58–15.65, ²⁰⁸Pb/²⁰⁴Pb 38.19–38.58. Sr-Nd values are negatively correlated and form a trend parallel to the mantle array, overlapping the field for ocean island basalts (OIB). The LBEJ rocks have similar ⁸⁷Sr/⁸⁶Sr values but lower ^Nd compared to basanitic rocks from the US Basin and Range Province (BRP). Pb isotopic ratios are positively correlated and overlap the braod fields for MORB and OIB and the small fields for Mexican ore deposits and volcanic rocks from the active subduction-related Mexican Volcanic Belt. The LBEJ rocks have slightly more radiogenic Pb than basanitic rocks from the US BRP. Despite correlations among the isotopic ratios of the LBEJ suite, none of these ratios correlate with position in the eruption sequence, Mg#, or any other compositional parameter. The two lower-crustal xenoliths have high ⁸⁷Sr/⁸⁶Sr values (0.707, 0.710) and low ^Nd (-1.5,-8.0) compared to the LBEJ volcanic rocks, but their Pb isotopic compositions are only slightly more radiogenic than the volcanic rocks. These data do not support the widely held view that the lower crust is a major reservoir of unradiogenic Pb. In order to further constrain the role played by crustal contamination in generating the isotopic diversity in the LBEJ suite, we conducted an extensive investigation of Sr–Nd–Pb isotopic ratios for scoria clasts from different levels of a single scoria-fall horizon in the pyroclastic sequence related to the formation of La Breña Maar. Our results do not support an important role for crustal contamination in the LBEJ magmas. Rather, we conclude that minor isotopic variability exists in the mantle source regions beneath the maar complex.     

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.     

Geochemistry, K–Ar geochronology and Sr–Nd–Pb isotope compositions of pitchstone in Gohado, southwestern Okcheon Belt, South Korea

Abstract Geochemical and Sr–Nd–Pb isotope characteristics, as well as K–Ar geochronology of a massive pitchstone (volcanic glass) stock erupted into Late Cretaceous lapilli tuff and rhyolite in the Gohado area, southwestern Okcheon Belt, South Korea, are reported. The pitchstones are highly evolved with SiO₂ contents ranging from ～72 to 73 wt%, K₂O/Na₂O ratios of 1.04–1.23 and low MgO/FeO^t values (0.17–0.20). The pitchstones are weakly peraluminous and the ASI (molar Al₂O₃/Na₂O + K₂O + CaO) values are significantly lower than 1.1. The pitchstones also display a general calc‐alkaline nature with significant alkali contents. The rare earth elements (REE) compositions show moderately fractionated nature with (La/Yb)_N ranging from 11 to 16. Chondrite normalized REE patterns show relative enrichment of light REE over heavy REE and moderate Eu anomaly (Eu/Eu* ratio varies from 0.53 to 0.57). A distinct negative Nb anomaly is observed for all pitchstones on a primitive mantle normalized trace element diagram, typical of subduction‐related magmatism and crustal‐derived granites. All these features are characteristic of I‐type granites derived from a continental arc. The pitchstones have Zr contents of 98.5–103.5 ppm with zircon thermometry yielding temperatures of 749–755°C (mean 752°C). The K–Ar analyses of representative pitchstone samples yielded ages of 58.7 ± 2.3 and 62.4 ± 2.1 Ma with a mean age of 61 Ma. The rocks show nearly uniform initial ⁸⁷Sr/⁸⁶Sr isotopic ratios of 0.7104–0.7106 and identical ¹⁴³Nd/¹⁴⁴Nd initial ratio of 0.5120. The rocks display negative εNd (61 Ma) values of ?12. The depleted mantle model ages (T_DM) range from 1.54 Ga to 1.57 Ga. The Pb isotope ratios are ²⁰⁶Pb/²⁰⁴Pb = 18.522–18.552, ²⁰⁷Pb/²⁰⁴Pb = 15.642–15.680 and ²⁰⁸Pb/²⁰⁴Pb = 38.794–38.923. These ratios suggest that the Gohado pitchstones were formed in a continental arc environment by partial melting of a 1.54 Ga to 1.57 Ga parental sources of lower crustal rocks probably of mafic or intermediate compositions.     

Space-time variations in British Caledonian Granites: some geophysical correlations

The characteristics of 30 “granites” from the postulated Caledonian (Iapetus Ocean) suture zone of mainland Britain are discussed. Geophysical (gravity, aeromagnetic), geochemical (U/Pb and initial⁸⁷Sr/⁸⁶Sr) and isotopic age data indicate that these British Caledonian intrusions (390–600 Ma) can be divided into two distinct groups temporally, each of which is further subdivided spatially.The temporal division applies throughout the British province and separates a pre-Silurian (group 1) suite of low-volume, low-mobility magmas, which were intruded under compressive conditions, from a Siluro-Devonian (group 2) suite of large volume, mobile magmas intruded under tensional conditions.The spatial subdivisions of groups 1 and 2 are made between intrusions emplaced to either side of the postulated ENE-WSW Iapetus Ocean suture which runs through the Solway Firth. First, the group 1 granites northwest of the suture probably were produced by partial fusion involving Proterozoic continental crust (group 1N) whereas those to the southeast have isotopic characteristics simply indicating a mantle or ocean crustal source (group 1S). Second, the Siluro-Devonian granites, which were all derived largely at the expense of Caledonian mantle, have different aeromagnetic expressions depending on their position in the northwest (2N) or southeast (2S) Caledonides. These aeromagnetic characteristics are probably related to the differences in basement structure recently identified by seismic surveys and they provide further evidence for the former existence and Siluro-Devonian closure of Iapetus. Another significant implication may be that Proterozoic basement is lacking from beneath the region immediately adjacent to and southeast of the suture — southern Scotland and most of England.     

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.     

Sr isotope evolution during chemical weathering of granites —Impact of relative weathering rates of minerals

The Sr isotopic systematics in the weathering profiles of biotite granite and granite porphyry in southern Jiangxi Province were investigated. The results showed that during the chemical weathering of granites, remarked fractionation occurred between Rb and Sr. During the early stages of chemical weathering of granites, the released Sr/Si and Sr/Ca ratios are larger than those of the parent rocks, and the leaching rate of Sr is higher than those of Si, Ca, K, Rb, etc. Dynamic variations in relative weathering rates of the main Sr-contributing minerals led to fluctuation with time in⁸⁷Sr/⁸⁶Sr ratios of inherent and released Sr in the weathering crust of granite. Successive weathering of biotite, plagioclase and K-feldspar made⁸⁷Sr/⁸⁶Sr ratios in the weathering residues show such a fluctuation trend as to decrease first, increase, and then decrease again till they maintain stable. This work further indicates that when Sr isotopes are used to trace biogeochemical processes on both the catchment and global scales, one must seriously take account of the preferential release of Sr from dissolving solid phase and the fluctuation of⁸⁷Sr/⁸⁶Sr ratios caused by the variations of relative weathering rates of Sr-contributing minerals.     

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).     

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.     

Sr, Nd, O and H isotopic ratios in Ascension Island lavas and plutonic inclusions; cogenetic origin

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

Sr and Nd isotope geochemistry of coexisting alkaline magma series,Cantal, Massif Central,France

Sr and Nd isotope analyses are presented for Tertiary continental alkaline volcanics from Cantal, Massif Central, France. The volcanics belong to two main magma series, silica-saturated and silica-undersaturated (with rare nephelinites). Trace element and isotopic data indicate a common source for the basic parental magmas of both major series; the nephelinites in contrast must have been derived from a mantle source which is isotopically and chemically distinct from that which gave rise to the basalts and basanites.⁸⁷Sr/⁸⁶Sr initial ratios range from 0.7034 to 0.7056 in the main magma series (excluding rhyolites) and¹⁴³Nd/¹⁴⁴Nd ratios vary between 0.512927 and 0.512669; both are correlated with increasing SiO₂ in the lavas. The data can be explained by a model of crustal contamination linked with fractional crystallisation. This indicates that crustal magma chambers are the sites of differentiation since only rarely do evolved magmas not show a crustal isotopic signature and conversely basic magmas have primitive isotopic ratios unless they contain obvious crustal-derived xenocrysts. Potential contaminants include lower crustal granulites or partial melts of upper crustal units. Equal amounts of contamination are required for both magma series, refuting hypotheses of selective contamination of the silica-saturated series.The isotopic characteristics of the apparently primary nephelinite lavas demonstrates widespread heterogeneity in the mantle beneath Cantal. Some rhyolites, previously thought to be extremely contaminated or to be crustally derived, are shown to have undergone post-emplacement hydrothermal alteration.     

Isotope geochemistry (Sr–Nd–Pb) and petrogenesis of leucite-bearing volcanic rocks from “Colli Albani” volcano, Roman Magmatic Province, Central Italy: inferences on volcano evolution and magma genesis

The “Colli Albani” composite volcano is made up of strongly silica-undersaturated leucite-bearing rocks. Magmas were erupted during three main periods, but a complex plumbing system dominated by regional tectonics channelled magmas into different reservoirs. The most alkali-rich magmas, restricted to the caldera-forming period (pre-caldera), are extremely enriched in incompatible trace elements and display more radiogenic Sr (⁸⁷Sr/⁸⁶Sr?=?0.71057–0.71067), with slightly less radiogenic Pb with respect to those of the post-caldera period. Post-caldera volcanic activity was concentrated in three different volcanic environments: external to the caldera, along the caldera edge and within the caldera. The post-caldera magmas produced melilite- to leucitite-bearing, plagioclase-free leucitites. In contrast to the pre-caldera lavas, they are characterised by lower incompatible trace element abundances and less radiogenic Sr (⁸⁷Sr/⁸⁶Sr?=?0.71006–0.71039). Magmas evolved through crystal fractionation plus minor crustal assimilation in a large magma chamber during the pre-caldera period. The multiple caldera collapses dissected and partially obliterated the early magma chamber. During the post-caldera stage, magmas were channelled through several pathways and multiple shallow-level magma reservoirs were established. A lithospheric mantle wedge previously depleted in the basaltic component and subsequently enriched by metasomatic slab-derived component is suggested as the mantle source of Colli Albani parental magmas. Two different parental magmas are recognised for the pre- and post-caldera stages. The differences may be related to the interplay between smaller degrees of melting for the pre-caldera magmas and more carbonate-rich recycled subducted lithologies in the post-caldera magmas.     

143Nd/144Nd,87Sr/86Sr and trace element constraints on the petrogenesis of Aleutian island arc magmas

¹⁴³Nd/¹⁴⁴Nd,⁸⁷Sr/⁸⁶Sr and trace element results are reported for volcanic and plutonic rocks of the Aleutian island arc. The Nd and Sr isotopic compositions plot within the mantle array with ε_Nd values of from 6.5 to 9.1 and⁸⁷Sr/⁸⁶Sr ratios of from 0.70289 to 0.70342. Basalts have mildly enriched light REE abundances but essentially unfractionated heavy REE abundances, while andesites exhibit a greater degree of light to heavy REE fractionation. Both the basalts and andesites have significant large ion lithophile element to light rare earth element (LILE/LREE) enrichments. Variations in the isotopic compositions of Nd and Sr are not related to the spatial distribution of volcanoes in the arc, nor are they related to temporal differences. ε_Nd and⁸⁷Sr/⁸⁶Sr do not correlate with major element compositions but do, however, correlate with certain LILE/LREE ratios (e.g. Ba_N/La_N). Plutonic rocks have isotropic and trace element characteristics identical to some of the volcanic rocks. Rocks that make up the tholeiitic, calc-alkaline and alkaline series in the Aleutians do not come from isotopically distinct sources, but do exhibit some differing LILE characteristics.Given these elemental and isotopic constraints it is shown that the Aleutian arc magmas could not have been derived directly from homogeneous MORB-type mantle, or fresh or altered MORB subducted beneath the arc. Mixtures of partially altered MORB with deep-sea sediment can in principle account for the isotopic characteristics and most of the observed LILE/LREE enrichments. However, some samples have exceedingly high LILE/LREE enrichments which cannot be accounted for by sediment contamination alone. For these samples a more complex scenario is considered whereby dehydration and partial melting of the subducted slab, containing less than 8% sediment, produces a LILE-enriched (relative to REE) metasomatic fluid which interacts with the overlying depleted mantle wedge. The isotopic and LILE characteristics of the mantle are extremely sensitive to metasomatism by small percentages of added fluid, whereas major elements are not substantially effected, Major element compositions of Aleutian magmas are dominantly controlled by the partial melting of this mantle and subsequent crystal fractionation; whereas isotopic and LILE characteristics are determined by localized mantle heterogeneities.     

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.     

Strontium and neodymium isotopic evidence for the heterogeneous nature and development of the mantle beneath Afar (Ethiopia)

Neodymium isotope and REE analyses of recent volcanic rocks and spinel lherzolite nodules from the Afar area are reported. The¹⁴³Nd/¹⁴⁴Nd ratios of the volcanic rocks range from 0.51286 to 0.51304, similar to the range recorded from Iceland. However, the⁸⁷Sr/⁸⁶Sr ratios display a distinctly greater range (0.70328–0.70410) than those reported from the primitive rocks of Iceland. Whole rock samples and mineral separates from the spinel lherzolite nodules exhibit uniform¹⁴³Nd/¹⁴⁴Nd ratios (ca. 0.5129) but varied⁸⁷Sr/⁸⁶Sr ratios in the range 0.70427–0.70528.The SrNd isotope variations suggest that the volcanic rocks may have been produced by mixing between two reservoirs with distinct isotopic compositions. Two possible magma reservoirs in this area are the source which produced the “MORB-type” volcanics in the Red Sea and Gulf of Aden and the anomalous source represented by the nodule suite. The isotopic composition of the volcanics is compatible with mixing between these two reservoirs.It is shown that the anomalous source with a high⁸⁷Sr/⁸⁶Sr ratio cannot have been produced by simple processes of partial melting and mixing within normal mantle. Instead the high⁸⁷Sr/⁸⁶Sr is equated with a fluid phase. A primitive cognate fluid, subducted seawater or altered oceanic lithosphere may have been responsible for the generation of the source with a high⁸⁷Sr/⁸⁶Sr ratio.