Pre-Cenozoic intra-plate magmatism along the Central Andes (17–34°S): Composition of the mantle at an active margin

Sr–Nd–Pb isotope ratios of alkaline mafic intra-plate magmatism constrain the isotopic compositions of the lithospheric mantle along what is now the eastern foreland or back arc of the Cenozoic Central Andes (17–34°S). Most small-volume basanite volcanic rocks and alkaline intrusive rocks of Cretaceous (and rare Miocene) age were derived from a depleted lithospheric mantle source with rather uniform initial ¹⁴³Nd/¹⁴⁴Nd ( 0.5127–0.5128) and ⁸⁷Sr/⁸⁶Sr ( 0.7032–0.7040). The initial ²⁰⁶Pb/²⁰⁴Pb ratios are variable (18.5–19.7) at uniform ²⁰⁷Pb/²⁰⁴Pb ratios (15.60 ± 0.05). A variety of the Cretaceous depleted mantle source of the magmatic rocks shows elevated Sr isotope ratios up to 0.707 at constant high Nd isotope ratios. The variable Sr and Pb isotope ratios are probably due to radiogenic growth in a metasomatized lithospheric mantle, which represents the former sub-arc mantle beneath the early Palaeozoic active continental margin. Sr–Nd–Pb isotope signatures of a second mantle type reflected in the composition of Cretaceous (one late Palaeozoic age) intra-plate magmatic rocks (¹⁴³Nd/¹⁴⁴Nd  0.5123, ⁸⁷Sr/⁸⁶Sr  0.704, ²⁰⁶Pb/²⁰⁴Pb  17.5–18.5, and ²⁰⁷Pb/²⁰⁴Pb  15.45–15.50) are similar to the isotopic composition of old sub-continental lithospheric mantle of the Brazilian Shield.

Published Nd and Sr isotopic compositions of Mesozoic to Cenozoic arc-related magmatic rocks (18–40°S) represent the composition of the convective sub-arc mantle in the Central Andes and are similar to those of the Cretaceous (and rare Miocene) intra-plate magmatic rocks. The dominant convective and lithospheric mantle type beneath this old continental margin is depleted mantle, which is compositionally different from average MORB-type depleted mantle. The old sub-continental lithospheric mantle did not contribute to Mesozoic to Cenozoic arc magmatism.     

Geochemical constraints on the origin of bimodal magmatism at the Okinawa Trough, an incipient back-arc basin

The magmatism at the axial zone of the middle Okinawa Trough, a young continental back-arc basin, comprises a bimodal basaltic–rhyolitic suite, accompanied by minor intermediate rocks. We report major and trace element and Sr–Nd isotopic data for the intermediate to silicic suites, to provide constraints on their petrogenesis. The rhyolites, recovered as lava and pumice, fall into three geochemical groups (type 1, 2, and 3 rhyolites). Type 1 rhyolites have ⁸⁷Sr/⁸⁶Sr (0.7040–0.7042) and ¹⁴³Nd/¹⁴⁴Nd (0.5128–0.5129) identical to those of associated basalts, and are characterized by highly fractionated REE patterns. Petrogenesis of type 1 rhyolites is explicable in terms of fractional crystallization of the associated basalt. In contrast, type 2 rhyolites and andesite have slightly higher ⁸⁷Sr/⁸⁶Sr (0.7044–0.7047) but similar ¹⁴³Nd/¹⁴⁴Nd (0.5128) compared to those of the basalts. The compositions of type 2 rhyolite and andesite can be explained by assimilation and fractional crystallization (AFC) processes of the basalt magma; quantitative analysis suggests assimilation/fractional crystallization (M_a/M_c) ratios of ≤0.05. Hybrid andesite generated by mixing of evolved basalt and type 1 rhyolite is also present. We emphasize that mechanical extension in this part of the Okinawa Trough involves gabbroic lower crust that resulted from fractionation of mantle-derived basaltic magmas. Type 3 rhyolite occurs only as pumice, which makes its derivation questionable. This rhyolite has major and trace element compositions and Sr–Nd isotopic ratios, which suggests that it may be derived from volcanic activity on the southern Ryukyu volcanic front, and arrived in the Okinawa Trough by drifting on the Kuroshio Current.     

Magmagenesis in a subduction-related post-collisional volcanic arc segment: the Ukrainian Carpathians

Calc-alkaline magmatism in the south-west Ukraine occurred between 13.8 and 9.1 Ma and formed an integral part of the Neogene subduction-related post-collisional Carpathian volcanic arc. Eruptions occurred contemporaneously in two parallel arcs (here termed Outer Arc and Inner Arc) in the Ukrainian part of the Carpathians. Outer Arc rocks, mainly andesites, are characterized by LILE enrichment (e.g. K and Pb), Nb depletion, low compatible trace element abundances, high ⁸⁷Sr/⁸⁶Sr, high δ¹⁸O and low ¹⁴³Nd/¹⁴⁴Nd isotopic ratios (0.7085–0.7095, 7.01–8.53, 0.51230–0.51245, respectively). Inner Arc rocks are mostly dacites and rhyolites with some basaltic and andesitic lavas. They also show low compatible element abundances but have lower ⁸⁷Sr/⁸⁶Sr, δ¹⁸O and higher ¹⁴³Nd/¹⁴⁴Nd ratios (0.7060–0.7085, 6.15–6.64, 0.5125–0.5126, respectively) than Outer Arc rocks. Both high-Nb and low-Nb lithologies are present in the Inner Arc. Based on the LILE enrichment (especially Pb), a higher fluid flux is suggested for the Outer Arc magmas compared with those of the Inner Arc.

Combined trace element and Sr–Nd–O isotopic modelling suggests that the factors which controlled the generation and evolution of magmas were complex. Compositional differences between the Inner and Outer Arcs were produced by introduction of variable proportions of slab-derived sediments and fluids into a heterogeneous mantle wedge, and by different extents of upper crustal contamination. Degrees of magmatic fractionation also differed between the two arcs. The most primitive magmas belong to the Inner Arc. Isotopic modelling shows that they can be produced by adding 3–8% subducted terrigenous flysch sediments to the local mantle wedge source. Up to 5% upper crustal contamination has been modelled for fractionated products of the Inner Arc. The geochemical features of Outer Arc rocks suggest that they were generated from mantle wedge melts similar to the Inner Arc primitive magmas, but were strongly affected by both source enrichment and upper crustal contamination. Assimilation of 10–20% bulk upper crust is required in the AFC modelling, assuming an Inner Arc parental magma. We suggest that magmagenesis is closely related to the complex geotectonic evolution of the Carpathian area. Several tectonic and kinematic factors are significant: (1) hydration of the asthenosphere during subduction and plate rollback directly related to collisional processes; (2) thermal disturbance caused by ascent of hot asthenospheric mantle during the back-arc opening of the Pannonian Basin; (3) clockwise translational movements of the Intracarpathian terranes, which facilitated eruption of the magmas.     

Petrogenesis of collision-related plutonics in Central Anatolia, Turkey

Central Anatolia exhibits good examples of calc-alkaline and alkaline magmatism of similar age in a collision-related tectonic setting (continent–island arc collision). In the Central Anatolia region, late Cretaceous post-collisional plutonic rocks intrude Palaeozoic–Mesozoic metamorphic rocks overthrust by Upper Cretaceous ophiolitic units to make up the Central Anatolian Crystalline Complex.

In the complex, three different intrusive rock types may be recognised based on their geochemical characteristics: (i) calc-alkaline (Behrekdag, Cefalikdag, and Celebi); (ii) subalkaline-transitional (Baranadag); and (ii) alkaline (Hamit). The calc-alkaline and subalkaline plutonic rocks are metaluminous I-type plutons ranging from monzodiorite to granite. The alkaline plutonic rocks are metaluminous to peralkaline plutons, predominantly A-type, ranging from nepheline monzosyenite to quartz syenite.

All intrusive rocks show enrichment in LILE and LREE relative to HFSE, and have high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd ratios. These characteristics indicate an enriched mantle source region(s) carrying a subduction component inherited from pre-collision subduction events. The tectonic discrimination diagram of Rb vs. (Y+Nb) suggests that the calc-alkaline, subalkaline, and alkaline plutonic rocks have been affected by crustal assimilation combined with fractional crystallisation processes.

The coexistence of calc-alkaline and alkaline magmatism in the Central Anatolian Crystalline Complex may be attributed to mantle source heterogeneity before collision. The former carries a smaller intraplate component and pre-subduction enrichment compared to the latter. Either thermal perturbation of the metasomatised lithosphere by delamination of the thermal boundary layer (TBL), or removal of a subducted plate (slab breakoff) is the likely mechanism for the initiation of the post-collisional magmatism in the Complex.     

Mantle diversity beneath the Colombian Andes, Northern Volcanic Zone: Constraints from Sr and Nd isotopes

In order to provide mantle and crustal constraints during the evolution of the Colombian Andes, Sr and Nd isotopic studies were performed in xenoliths from the Mercaderes region, Northern Volcanic Zone, Colombia. Xenoliths are found in the Granatifera Tuff, a deposit of Cenozoic age, in which mantle- and crustal-derived xenoliths are present in bombs and fragments of andesites and lamprophyres compositions. Garnet-bearing xenoliths are the most abundant mantle-derived rocks, but websterites (garnet-free xenoliths) and spinel-bearing peridotites are also present in minor amounts. Amphibolites, pyroxenites, granulites, and gneisses represent the lower crustal xenolith assemblage. Isotopic signatures for the mantle xenoliths, together with field, petrographic, mineral, and whole-rock chemistry and pressure–temperature estimates, suggest three main sources for these mantle xenoliths: garnet-free websterite xenoliths derived from a source region with low P and T (16 kbar, 1065 °C) and MORB isotopic signature, ⁸⁷Sr/⁸⁶Sr ratio of 0.7030, and ¹⁴³Nd/¹⁴⁴Nd ratio of 0.5129. Garnet-bearing peridotite and websterite xenoliths derived from two different sources in the mantle: i) a source with intermediate P and T (29–35 kbar, 1250–1295 °C) conditions, similar to that of sub-oceanic geotherm, with an OIB isotopic signature (⁸⁷Sr/⁸⁶Sr ratio of 0.7043 and ¹⁴³Nd/¹⁴⁴Nd ratio of 0.5129); and ii) another source with P and T conditions similar to those of a sub-continental geotherm (>38 kbar, 1140–1175 °C) and OIB isotopic characteristics (⁸⁷Sr/⁸⁶Sr ratio=0.7041 and ¹⁴³Nd/¹⁴⁴Nd ratio=0.5135).     

The late Cretaceous lithospheric mantle beneath the Central Andes: Evidence from phase equilibria and composition of mantle xenoliths

Temperature estimates and chemical composition of mantle xenoliths from the Cretaceous rift system of NW Argentina (26°S) constrain the rift evolution and chemical and physical properties of the lithospheric mantle at the eastern edge of the Cenozoic Andean plateau. The xenolith suite comprises mainly spinel lherzolite and subordinate pyroxenite and carbonatized lherzolite. The spinel lherzolite xenoliths equilibrated at high-T (most samples >1000 °C) and P below garnet-in. The Sm–Nd systematics of compositionally unzoned clino- and orthopyroxene indicate a Cretaceous minimum age for the high-T regime, i.e., the asthenosphere/lithosphere thermal boundary was at ca. 70 km depth in the Cretaceous rift. Major elements and Cr, Ni, Co and V contents of the xenoliths range between values of primitive and depleted mantle. Calculated densities based on the bulk composition of the xenoliths are <3280 kg/m³ for the estimated P–T conditions and indicate a buoyant, stable upper mantle lithosphere. The well-equilibrated metamorphic fabric and mineral paragenesis with the general lack of high-T hydrous phases did not preserve traces of metasomatism in the mantle xenoliths. Late Mesozoic metasomatism, however, is obvious in the gradual enrichment of Sr, U, Th and light to medium REE and changes in the radiogenic isotope composition of an originally depleted mantle. These changes are independent of the degree of depletion evidenced by major element composition. ¹⁴³Nd/¹⁴⁴Nd_i ratios of clinopyroxene from the main group of xenoliths decrease with increasing Nd content from >0.5130 (depleted samples) to ca. 0.5127 (enriched samples). ⁸⁷Sr/⁸⁶Sr_i ratios (0.7127–0.7131, depleted samples; 0.7130–0.7134, enriched samples) show no variation with variable Sr contents. Pb_i isotope ratios of the enriched samples are rather radiogenic (²⁰⁶Pb/²⁰⁴Pb_i 18.8–20.6, ²⁰⁷Pb/²⁰⁴Pb_i 15.6–15.7, ²⁰⁸Pb/²⁰⁴Pb_i 38.6–47) compared with the Pb isotope signature of the depleted samples. The large scatter and high values of ²⁰⁸Pb/²⁰⁴Pb_i ratios of many xenoliths indicates at least two Pb sources that are characterized by similar U/Pb but by different Th/Pb ratios. The dominant mantle type in the investigated system is depleted mantle according to its Sr and Nd isotopic composition with relatively radiogenic Pb isotope ratios. This mantle is different from the Pacific MORB source and old subcontinental mantle from the adjacent Brazilian Shield. Its composition probably reflects material influx into the mantle wedge during various episodes of subduction that commenced in early Paleozoic or even earlier. Old subcontinental mantle was already replaced in the Paleozoic, but some inheritance from old mantle lithosphere is represented by rare xenoliths with isotope signatures indicating a Proterozoic origin.     

Mixing of asthenospheric and lithospheric mantle-derived basalt magmas as shown by along-arc variation in Sr and Nd isotopic compositions of Early Miocene basalts from back-arc margin of the NE Japan arc

We report trace element and Sr–Nd isotopic compositions of Early Miocene (22–18 Ma) basaltic rocks distributed along the back-arc margin of the NE Japan arc over 500 km. These rocks are divided into higher TiO₂ (> 1.5 wt.%; referred to as HT) and lower TiO₂ (< 1.5 wt.%; LT) basalts. HT basalt has higher Na₂O + K₂O, HFSE and LREE, Zr/Y, and La/Yb compared to LT basalt. Both suite rocks show a wide range in Sr and Nd isotopic compositions (initial ⁸⁷Sr/⁸⁶Sr (SrI) = 0.70389 to 0.70631, initial ¹⁴³Nd/¹⁴⁴Nd(NdI) = 0.51248 to 0.51285). There is no any systematic variation amongst the studied Early Miocene basaltic rocks in terms of Sr–Nd isotope or Na₂O + K₂O and K₂O abundances, across three volcanic zones from the eastern through transitional to western volcanic zone, but we can identify gradual increases in SrI and decreases in NdI from north to south along the back-arc margin of the NE Japan arc. Based on high field strength element, REE, and Sr–Nd isotope data, Early Miocene basaltic rocks of the NE Japan back-arc margin represent mixing of the asthenospheric mantle-derived basalt magma with two types of basaltic magmas, HT and LT basaltic magmas, derived by different degrees of partial melting of the subcontinental lithospheric mantle composed of garnet-absent lherzolite, with a gradual decrease in the proportion of asthenospheric mantle-derived magma from north to south. These mantle events might have occurred in association with rifting of the Eurasian continental arc during the pre-opening stage of the Japan Sea.     

Geochemistry of post-collisional mafic lavas from the North Anatolian Fault zone, Northwestern Turkey

Extensive magmatic activity developed at the northwestern part of the Anatolian block and produced basaltic lavas that are situated along and between the two segments of the North Anatolian Fault zone. This region is a composite tectonic unit formed by collision of continental fragments after consumption of Neotethyan ocean floor during the late Cretaceous. Northwestern Anatolian basalts and evolved lavas exhibit both tholeiitic and calc-alkaline characteristics. Mafic lavas are moderately enriched in LILE (except depleted part of Yuvacık and İznik samples) and depleted in HFSE (but not Zr, Hf) relative to primitive mantle values, suggesting derivation from a MORB-like mantle source that is unexpected in this subduction environment. Sr and Nd isotopes are close to the mantle array and vary beyond analytical error (⁸⁷Sr/⁸⁶Sr 0.70404–0.70546, ¹⁴³Nd/¹⁴⁴Nd 0.51270–0.51289). These geochemical features may result from two possible processes: (1) melting of a MORB-like mantle source that was modified by subduction-released fluids and melts or (2) modification of mafic liquids derived from a dominantly MORB-like source by crustal or lithospheric mantle material. Geochemical characteristics of the lavas (e.g., Ba/Rb, Rb/Sr, Ba/Zr, ⁸⁷Sr/⁸⁶Sr, Sr/P) vary systematically along the fault zone from east to west, consistent with a decrease in the degree of melting from east to west or a change in the nature of the source composition itself. Thus, the difference in incompatible elements and Sr–Nd isotopic ratios seems to result from small-scale mantle heterogeneity in a post-collisional tectonic environment.     

The Dodecanese Province, SE Aegean: A model for tectonic control on potassic magmatism

In the south-eastern Aegean several composite Upper Miocene volcanoes have erupted a variety of extrusive and intrusive rocks of mainly intermediate composition with potassic affinities. This study discusses the tectonic setting of this distinct igneous province (Dodecanese Province, DP) and presents mineralogical, geochemical and isotopic (Sr, Nd) characteristics of mafic rocks from two of its centers (Bodrum, Turkey and Samos, Greece). The mafics fall in two groups: ultrapotassics in Bodrum and shoshonitic rocks in Bodrum and Samos, with their geochemical signature varying from typical arc-like (Bodrum) to weakly orogenic (Bodrum, Samos).

The Bodrum ultrapotassic rocks are unusual and important in that while they display the petrological and geochemical characteristics of primary mantle-derived magmas they are also extraordinary LIL element-enriched. Their initial Sr and Nd isotopic compositions (⁸⁷Sr⁸⁶Sr =0. 7071; ¹⁴³Nd/¹⁴⁴Nd = 0.512465) lie at one extreme of the Bodrum-Samos range (⁸⁷Sr⁸⁶Sr = 0.7052−0.7071; ¹⁴³Nd/¹⁴⁴Nd = 0/51246−0.51264) and are evidence for the existence of an “enriched mantle” component.

Geochemical characteristics, including Nd- and Sr-isotope data, are used to discuss source component mixing arrays defined by a wide range of circum-Mediterranean igneous provinces including the DP suites. At least three endmembers are required: (1) enriched mantle, (2) depleted mantle and (3) continental crust. The enriched mantle is most probably part of the sub-continental lithosphere which may be regionally distributed throughout the Mediterranean. Enrichment by emplacement of small fractions of melts of the depleted mantle can yield such a source if the enrichment is ancient (≈1.25 Ga). Crustal involvement may be the product of the extensive role of AFC processes operating both close to the Moho and in higher level magma chambers.

The location of the DP in the transitional margin of the Aegean zone of extension may partly explain the survival to upper crustal levels of emplacement, of unmixed, ultrapotassic melts of the enriched heterogeneities in the lithospheer. Changes in Ti/Zr ratio implicate the buffering role of a titanate in the lithosphere. Loss of orogenic geochemical signature and depletion in potassium content in recent volcanics in Western Anatolia imply an increased role of depleted mantle.     

Geochemical and isotope data from the Acatlán Volcanic Field, western Trans-Mexican Volcanic Belt: Origin and evolution

The Quaternary Acatlán Volcanic Field (AVF) is located at the western edge of the Trans-Mexican Volcanic Belt (TMVB). This region is related to the subduction of the Pacific Cocos and Rivera plates beneath the North American plate since the late Miocene. AVF rocks are products of Pleistocene volcanic activity and include lava flows, domes, erupted basaltic andesite, trachyandesite, trachydacite, and rhyolite of calc–alkaline affinity. Most rocks show depletion in high field-strength elements and enrichment in large ion lithophile elements and light rare earth elements as is typical for magmas in subduction-related volcanic arcs. ⁸⁷Sr/⁸⁶Sr values range from 0.70361 to 0.70412, while Nd values vary from +2.3 to +5.2. Sr–Nd isotopic data plot along the mantle array. On the other hand, lead isotope compositions (²⁰⁶Pb/²⁰⁴Pb=18.62–18.75, ²⁰⁷Pb/²⁰⁴Pb=15.57–15.64, and ²⁰⁸Pb/²⁰⁴Pb=38.37–38.67) give evidence for combined influences of the upper mantle, fluxes derived from subducted sediments, and the upper continental crust involved in magma genesis at AVF. Additionally δ¹⁸O whole rock analyses range from +6.35‰ in black pumice to +10.9‰ in white pumice of the Acatlán Ignimbrite. A fairly good correlation is displayed between Sr as well as O isotopes and SiO₂ emphasizing the effects of crustal contamination. Compositional and isotopic data suggest that the different AVF series derived from distinct parental magmas, which were generated by partial melting of a heterogeneous mantle source.     

特提斯喜马拉雅带江孜地区古近纪地层源区分析——对造山带早期地壳加厚的制约

特提斯喜马拉雅北亚带江孜地区上古新统-下始新统甲查拉组记录了喜马拉雅碰撞造山带的早期地壳加厚和沉积历史。本文我们报道了甲查拉组详细的碎屑锆石U-Pb年龄和全岩Sm-Nd同位素数据。甲查拉组由青灰色厚层的岩屑砂岩夹泥岩组成,不整合覆盖在宗卓组之上,碎屑锆石主要的峰值介于350～80 Ma, 900～470 Ma以及1 300～950 Ma,次要的峰值介于2 800～1 500 Ma。全岩⁸⁷Sr/⁸⁶Sr介于0.707 505～0.713 174,¹⁴³Nd/¹⁴⁴Nd介于0.512 206～0.512 355,ε_Nd(0)介于-5.52～-8.43。甲查拉组物源区以再循环的日喀则弧前盆地和上三叠统郎杰学群为主,少量物质来自雅鲁藏布江缝合带。上述研究表明,甲查拉组沉积在周缘前陆盆地的背景下,且特提斯喜马拉雅北亚带在始新世期间经历了明显的地壳加厚。     

Origin of lamprophyres by the mixing of basic and alkaline melts in magma chamber in Beiya area, western Yunnan, China

Lamprophyres consisting mainly of diopside, phlogopite and K-feldspar formed in the early Tertiary around 60 Ma in the Beiya area and are characterized by low SiO₂ ± 46–50 wt.%), Rb (31–45 ppm) and Sr (225–262 ppm), high Al₂O₃, (11.2–13.1 wt.%), CaO (8.0–8.7 wt.%), MgO (11.5–12.1 wt.%), K₂O(4.9–5.5 wt.%), TiO₂ (2.9–3.3 wt.%) and REE (174–177 ppm), and compatible elements (e.g. Sc, Cr and Ni) and HSF elements (e.g. Th, U, Zr, Nb, Ta, Ti and Y), and low ¹⁴³Nd/¹⁴⁴Nd 0.512372–0.512536, middle ⁸⁷Sr/⁸⁶Sr 0.707322–0.707395, middle ²⁰⁶Pb/²⁰⁴Pb 18.50–18.59, ²⁰⁷Pb/²⁰⁴Pb 15.60–15.65 and ²⁰⁸Pb/²⁰⁴Pb 38.75–38.8. These rocks developed peculiar quartz megacrysts with poly-layer reaction zones, melt inclusions, and partial melted K-feldspar and plagioclase inclusions, and plastic shapes. Important features of these rocks include: (1) hybrid composition of elements, (2) abrupt increase of SiO₂ content of the melt, recorded by zoned diopside, (3) development of sanidine and aegirine-augite reaction zones, (4) alkaline melt and partial melted K-feldspar and plagioclase inclusions, (5) deformed quartz inclusions associated with quartz megacrysts, (6) the presence of quartz megacrysts in plastic shape with their parent melts, (7) the occurrence of olivine, high-MgO ilmenite and spinel inclusions within earlier formed diopside, phlogopite and magnetite. Median ⁸⁷Sr/⁸⁶Sr values between Tertiary alkaline porphyries in the Beiya area and the western Yunnan and Tertiary basalt in the western Yunnan indicate that the Beiya lamprophyre melts were derivative and resulted from the mixing between basic melts that were related to the partial melting of phenocrysts of spinel iherzolite from a mantle source. The alkaline melts originated from partial melting along the Jinshajiang subduction ductile shear zone at the contact between the buried Palaeo-Tethyan oceanic lithosphere and the upper mantle lithosphere. The alkaline melts are composed of 65% sanidine (Or₇₀Ab₂₈An₂) and 35% SiO₂. The melt mixing occurred in magma chambers in the middle-shallow crust at 8–10 km before the derivative lamprophyre melts intruded into the shallow cover in Beiya area. This mixing of basic and alkaline melts might represent a general process for the formation of lamprophyre in the western Yunnan.     

Modeling of subduction components in the Genesis of the Meso-Cenozoic igneous rocks from the South Shetland Arc, Antarctica

Isotope data and trace elements concentrations are presented for volcanic and plutonic rocks from the Livingston, Greenwich, Robert, King George and Ardley islands (South Shetland arc, Antarctica). These islands were formed during subduction of the Phoenix Plate under the Antarctica Plate from Cretaceous to Tertiary. Isotopically (⁸⁷Sr/⁸⁶Sr)_o ratios vary from 0.7033 to 0.7046 and (¹⁴³Nd/¹⁴⁴Nd)_o ratios from 0.5127 to 0.5129. εNd values vary from +2.71 to +7.30 that indicate asthenospheric mantle source for the analysed samples. ²⁰⁸Pb/²⁰⁴Pb ratios vary from 38.12 to 38.70, ²⁰⁷Pb/²⁰⁴Pb ratios are between 15.49 and 15.68, and ²⁰⁶Pb/²⁰⁴Pb from 18.28 to 18.81. The South Shetland rocks are thought to be derived from a depleted MORB mantle source (DMM) modified by mixtures of two enriched mantle components such as slab-derived melts and/or fluids and small fractions of oceanic sediment (EM I and EM II). The isotopic compositions of the subduction component can be explained by mixing between at least 4 wt.% of sediment and 96 wt.% of melts and/or fluids derived from altered MORB.     

Andean subduction-related mantle xenoliths: Isotopic evidence of Sr–Nd decoupling during metasomatism

Sr–Nd isotopic analyses on some mantle xenolith samples from the Northern, Southern and Austral Andean volcanic zones exhibit radiogenic Sr enrichment without dramatic changing of the Nd isotopic composition. This anomalous effect (Sr–Nd decoupling) makes these samples plot displaced to the right side of the “mantle array” trend (here called the “MORB–OIB–BSE trend”) in the ⁸⁷Sr/⁸⁶Sr vs. ¹⁴³Nd/¹⁴⁴Nd isotopic diagram. Such behavior reflects processes that took place in the mantle and can be related to: i) the mixture of a depleted mantle and an enriched source (enriched mantle II—EMII); ii) the mixture of a depleted mantle and a mixture of mantle-derived and slab-derived melts; and iii) a chromatographic process that occurs during the percolation of a metasomatic agent through the mantle.     

Sr and O isotope constraints on source and crustal contamination in the high-K calc-alkaline and shoshonitic neogene volcanic rocks of SE Spain

The Neogene volcanic province of SE Spain (NVPS) is characterized by calc-alkaline (CA), high-K calc-alkaline (KCA), shoshonitic (SH), ultrapotassic (UP), and alkaline basaltic (AB) volcanic series. All these series, except the AB, have high LILE/LREE, LILE/HFSE and B/Be ratios and high but variable Sr, Pb and O isotope compositions. The KCA and SH lavas contain metapelitic xenoliths whose mineralogical and chemical composition are typical of anatectic restites. The geochemical characteristics of CA, KCA, SH and UP series suggest that they originated from the lithospheric mantle, previously contaminated by fluids derived from pelagic sediments. Additionally, the presence of restite xenoliths in the KCA and SH lavas indicates some sort of interaction between the mantle-derived magmas and the continental crust. Trace element and isotope modeling for the KCA and SH lavas and the restites, point towards the existence of two mixing stages. During the first stage, the lithospheric mantle was contaminated by 1–5% of fluids derived from pelagic sediments, which produced a fertile source heterogeneously enriched in incompatible elements (particularly LILE and LREE), as well as in ⁸⁷Sr/⁸⁶Sr, without significant modifications of the δ¹⁸O values. In the second stage, the primary melts derived from this metasomatized mantle, which inherited the enrichment in LILE, LREE and ⁸⁷Sr/⁸⁶Sr, interacted with crustal liquids from the Betic Paleozoic basement during their ascent towards the surface. This mixing process caused an increase in δ¹⁸O values and, to a lesser extent, in ⁸⁷Sr/⁸⁶Sr ratios. However, the incompatible trace elements abundances only change slightly, even for high mixing rates, due to their similar concentrations in both components. We suggest the following geodynamic scenario to account for the global evolution of this area: (1) a Late Cretaceous to Oligocene subduction scheme during which mantle metasomatism took place, shortly followed by Upper Oligocene to Lower Miocene continental collision, and (2) a Middle to Upper Miocene extensional event triggering partial melting of the previously metasomatized mantle and the extrusion of the CA and associated magmas.     

Rifting-related volcanism in an oceanic post-collisional setting: the Tabar–Lihir–Tanga–Feni (TLTF) island chain, Papua New Guinea

The Tabar–Lihir–Tanga–Feni (TLTF) volcanic island chain occurs in a zone of lithospheric extension superimposed on a post-collisonal tectonic setting along the Pacific and Indo-Australian plates northeast of Papua New Guinea. We present geochemical and Sr, Nd, and Pb isotope data for volcanic rocks from these islands and three recently discovered seamounts located at Lihir island. Major element data document an alkalic affinity of the sample suite and trachybasalts as the predominant rock type. Negative Nb-anomalies in extended trace element patterns, enrichment of the light rare earth elements, and Ce/Pb ratios of about 4 are typical of the values in calc alkaline island arc volcanics and support an origin from subduction-modified mantle. ⁸⁷Sr/⁸⁶Sr ratios of 0.7037 to 0.7044 and _Nd values of +5.6 to +6.8 indicate that the upper mantle evolved with a time-integrated depletion in LREE, however, not as severe as that recorded in basalts from the East Pacific Rise. Variable ⁸⁷Sr/⁸⁶Sr ratios at less variable ¹⁴³Nd/¹⁴⁴Nd ratios suggest that ⁸⁷Sr/⁸⁶Sr ratios of the melts were modified by secondary processes, such as assimilation of seawater Sr from crustal rocks. The Pb isotope ratios are uniform, moderately radiogenic (²⁰⁶Pb/²⁰⁴Pb ca. 18.7 to 18.8), and similar to those reported for the active Mariana arc. Elevated ²⁰⁷Pb/²⁰⁴Pb ratios relative to Pacific MORB suggest melting of small amounts of subducted sediments (ca. 1–2 wt.%). An important control of subducted sediment on the chemistry of the melts can also be inferred from the ratios of highly incompatible trace elements (e.g., Th, U, Pb, La, and Nb). Additional mantle enrichment by subduction derived fluids is reflected in high values of highly incompatible trace element ratios between fluid mobile (e.g., Ba) and fluid immobile elements (e.g., Th, Nb). The results of this study document that the chemical composition of igneous rocks from post-collisional tectonic settings are strongly influenced by previous plate tectonics. This conclusion implies that the information conveyed by tectonic discrimination diagrams for these rocks must be interpreted with care.     

Bimodal back-arc alkaline magmatism after ridge subduction: Pliocene felsic rocks from Central Patagonia (47°S)

Volumetrically minor microsyenites, alkali microgranite and related trachytic dykes intrude early Pliocene OIB-like alkali basaltic and basanitic flows of the Meseta del Lago Buenos Aires in Central Patagonia (47°S–71°30′W), and occur together with scarce trachytic lava flows. Whole-rock K–Ar ages between 3.98 and 3.08 Ma indicate that the emplacement of these felsic rocks occurred more or less synchronously with that of the post-plateau basaltic sequence that they intrude, during a bimodal mafic–felsic magmatic episode devoid of intermediate compositions. Chemically, these rocks have A₁-type granitoid affinities and are characterized by high silica and alkali contents (60–68 wt.% SiO₂; 8.7–10.8 wt.% Na₂O + K₂O), major and trace elements patterns evidencing evolution by low-pressure fractional crystallization, and Sr and Nd isotopic signatures similar to those of coeval basalts ((⁸⁷Sr/⁸⁶Sr)_o = 0.70488–0.70571; (¹⁴³Nd/¹⁴⁴Nd)_o = 0.512603–0.512645). Nevertheless, some of them have the most radiogenic Sr values ever reported for a magmatic rock in the Meseta and even in the whole Neogene Patagonian Plateau Lavas province ((⁸⁷Sr/⁸⁶Sr)_o = 0.70556–0.70571; (¹⁴³Nd/¹⁴⁴Nd)_o = 0.512603–0.512608). In addition, very high contents of strongly incompatible elements in the most evolved rocks, together with Sr isotopic ratios higher than those of coeval basalts, suggest the occurrence of open-system magmatic processes. Continuous fractional crystallization from a primitive basaltic source, similar to post-plateau coeval basalts, towards alkali granites combined with small rates of assimilation of host Jurassic tuffs (AFC) in a shallow magmatic reservoir, best explains the geochemical and petrographic features of the felsic rocks. Therefore, A₁-type magmatic rocks can be generated by open-system crystallization of deep asthenospheric melts in back-arc tectonic settings.

In Central Patagonia, these  3–4 Ma old alkaline intrusions occur aligned along a  N160–170 trending lineament, the Zeballos Fault Zone, stacking the morphotectonic front of one segment of the Patagonian Cordillera. Intrusion along this fault zone occurred during the onset of a new transtensional or extensional event in the area, related to major regional tectonics occurring in possible relation with the collision of one segment of the Chile Spreading Ridge with the trench.     

新特提斯洋晚白垩世演化特点:来自泽当共国日二长花岗岩年代学、地球化学及Sr-Nd同位素证据

为加深对西藏泽当地区新特提斯洋演化的认识,对西藏泽当蛇绿混杂岩带内的共国日二长花岗岩进行了岩石学、岩石地球化学、同位素及年代学等研究,研究显示:共国日二长花岗岩岩体规模小、岩性稳定,LA-ICP-MS锆石U-Pb年龄为(90.40±0.68)Ma,属晚白垩世;岩石地球化学具高硅、富铝、富钾、低钛和准铝质钙碱性花岗岩特征;轻稀土富集、重稀土亏损,具明显的负Eu异常,微量元素表现为相对富集Rb、K、Ba、Th、U等大离子亲石元素,显著亏损Nb、P、Ti等高场强元素;(⁸⁷Sr/⁸⁶Sr)_i=0.705 708~0.706 284,(¹⁴³Nd/¹⁴⁴Nd)_i=0.512 689~0.512 716,ε_Nd(t)=2.00~2.51。以上特征表明,位于泽当蛇绿混杂岩带内的共国日二长花岗岩属于I型花岗岩,由正常岛弧岩浆形成,应为晚白垩世新特提斯洋向北俯冲形成的岛弧环境下俯冲带上部地壳部分熔融的产物,其不属于泽当蛇绿岩的组成部分,表明在90 Ma前泽当洋内弧已经消失。     

Isotopic equilibrium/disequilibrium in granites, metasedimentary rocks and migmatites (Damara orogen, Namibia)—a consequence of polymetamorphism and melting

The overwhelming part of the continental crust in the high-grade part of the Damara orogen of Namibia consists of S-type granites, metasedimentary rocks and migmatites. At Oetmoed (central Damara orogen) two different S-type granites occur. Their negative ε_Nd values (− 3.3 to − 5.9), moderately high initial ⁸⁷Sr/⁸⁶Sr ratios (0.714–0.731), moderately high ²⁰⁶Pb/²⁰⁴Pb (18.21–18.70) and ²⁰⁸Pb/²⁰⁴Pb (37.74–37.89) isotope ratios suggest that they originated by melting of mainly mid-Proterozoic metasedimentary material. Metasedimentary country rocks have initial ε_Nd of − 4.2 to − 5.6, initial ⁸⁷Sr/⁸⁶Sr of 0.718–0.725, ²⁰⁶Pb/²⁰⁴Pb ratios of 18.32–18.69 and ²⁰⁸Pb/²⁰⁴Pb ratios of 37.91–38.45 compatible with their variation in Rb/Sr, U/Pb and Th/Pb ratios. Some migmatites and residual metasedimentary xenoliths tend to have more variable ε_Nd values (initial ε_Nd: − 4.2 to − 7.1), initial Sr isotope ratios (⁸⁷Sr/⁸⁶Sr: 0.708–0.735) and less radiogenic ²⁰⁶Pb/²⁰⁴Pb (18.22–18.53) and ²⁰⁸Pb/²⁰⁴Pb (37.78–38.10) isotope compositions than the metasedimentary rocks. On a Rb–Sr isochron plot the metasedimentary rocks and various migmatites plot on a straight line that corresponds to an age of c. 550 Ma which is interpreted to indicate major fractionation of the Rb–Sr system at that time. However, initial ⁸⁷Sr/⁸⁶Sr ratios of the melanosomes of the stromatic migmatites (calculated for their U–Pb monazite and Sm–Nd garnet ages of c. 510 Ma) are more radiogenic (⁸⁷Sr/⁸⁶Sr: 0.725) than those obtained on their corresponding leucosomes (⁸⁷Sr/⁸⁶Sr: 0.718) implying disequilibrium conditions during migmatization that have not lead to complete homogenization of the Rb–Sr system. However, the leucosomes have similar Nd isotope characteristics than the inferred residues (melanosomes) indicating the robustness of the Sm–Nd isotope system during high-grade metamorphism and melting. On a Rb–Sr isochron plot residual metasedimentary xenoliths show residual slopes of c. 66 Ma (calculated for an U–Pb monazite age of 470 Ma) again indicating major fractionation of Rb/Sr at c. 540 Ma. However, at 540 Ma, these xenoliths have unradiogenic Sr isotope compositions of c. 0.7052, indicating depleted metasedimentary sources at depth. Based on the distinct Pb isotope composition of the metasedimentary rocks and S-type granites, metasedimentary rocks similar to the country rocks are unlikely sources for the S-type granites. Moreover, a combination of Sr, Nd, Pb and O isotopes favours a three-component mixing model (metasedimentary rocks, altered volcanogenic material, meta-igneous crust) that may explain the isotopic variabilty of the granites. The mid-crustal origin of the different types of granite emphasises the importance of recycling and reprocessing of pre-existing differentiated material and precludes a direct mantle contribution during the petrogenesis of the orogenic granites in the central Damara orogen of Namibia.     

Erosion of lithospheric mantle beneath the East African Rift system: geochemical evidence from the Kivu volcanic province

This study presents new major and trace element and Sr–Nd isotopic results for a suite of Miocene–Recent mafic lavas from the Kivu volcanic province in the western branch of the East African Rift. These lavas exhibit a very wide range in chemical and isotopic characteristics, due to a lithospheric mantle source region that is heterogeneous on a small scale, probably <1 km. The chemical and isotopic variations are mostly geographically controlled: lavas from Tshibinda volcano, which lies on a rift border fault on the northwestern margin of the province, have higher values of ⁸⁷Sr/⁸⁶Sr, (La/Sm)_n, Ba/Nb, and Zr/Hf than the majority of Kivu (Bukavu) samples. The range of ⁸⁷Sr/⁸⁶Sr at Tshibinda (0.70511–0.70514) overlaps some compositions found in the neighboring Virunga province, while Bukavu group lavas include the lowest ⁸⁷Sr/⁸⁶Sr (0.70314) and highest _Nd (+7.6) yet measured in western rift lavas. The Tshibinda compositions trend towards a convergence for Sr–Nd–Pb isotopic values among western rift lavas. Among Kivu lavas, variations in ¹⁴³Nd/¹⁴⁴Nd correlate with those for certain incompatible trace element ratios (e.g., Th/Nb, Zr/Hf, La/Nb, Ba/Rb), with Tshibinda samples defining one compositional extreme. There are covariations of isotopic and trace element ratios in mafic lavas of the East African Rift system that vary systematically with geographic location. The lavas represent a magmatic sampling of variations in the underlying continental lithospheric mantle, and it appears that a common lithospheric mantle (CLM) source is present beneath much of the East African Rift system. This source contains minor amphibole and phlogopite, probably due to widespread metasomatic events between 500 and 1000 Ma. Lava suites which do not show a strong component of the CLM source, and for which the chemical constraints also suggest the shallowest magma formation depths, are the Bukavu group lavas from Kivu and basanites from Huri Hills, Kenya. The inferred extent of lithospheric erosion therefore appears to be significant only beneath these two areas, which is generally consistent with lithospheric thickness variations estimated from gravity and seismic studies.