Development of Archaean lithosphere deduced from chronology and isotope chemistry of Scourie Dykes

The chronology and isotope geochemistry of a selection of Proterozoic Scourie dykes has been investigated in order to specify both their time of emplacement within the thermal history of the Archaean crust of N.W. Scotland, and to attempt to characterise the evolution of continental lithosphere. SmNd, RbSr and UPb isotope analyses are presented. Primary, major igneous minerals separated from four well preserved dykes yield SmNd ages of 2.031 ± 0.062Ga, 2.015 ± 0.042Ga, 1.982 ± 0.044Ga and 2.101 ± 0.078Ga, which are interpreted as crystallisation ages.The initial Nd isotope compositions in the dykes at their emplacement age of 2.0 Ga, range from +3.4 to −6.8, indicating the presence of an older lithospheric component. SmNd whole-rock isotope data for fifteen dykes, if interpreted to have age significance, yield an “age” of 3.05 ± 0.27 Ga. SmNd crustal residence ages for the same dykes average 2.95 Ga, which is interpreted as the time that small melts were added to the Lewisian lithosphere. The possibility that correlated¹⁴⁷Sm/¹⁴⁴Nd and¹⁴³Nd/¹⁴⁴Nd ratios are an artifact of mixing between depleted mantle melts generated at 2.0 Ga, and an older enriched lithospheric component is not eliminated by the data, but the relationship between 1/Nd and¹⁴³Nd/¹⁴⁴Nd ratios rules out any simple mixing. UPb isotope data for plagioclase feldspars and whole-rock samples of dykes provide useful estimates of initial Pb-isotope composition of the dykes at the time of their emplacement. Initial²⁰⁶Pb/²⁰⁴Pb and²⁰⁷Pb/²⁰⁴Pb ratios vary considerably and range from 13.98 to 15.78, and 14.72 to 15.56 respectively, and suggest that the UPb fractionation responsible must have occurred at least 2.5 Ga ago.The Scourie dykes have inherited a trace element enriched component from the Lewisian lithosphere, which has resided there since ca. 3 Ga ago. Whether the dykes inherited this material from the crust or the mantle portions of the lithosphere or both, it seems likely that small basaltic melts derived from asthenospheric mantle were ultimately responsible for the enrichment. The simplest view is that these small melt fractions had been resident in the mantle part of the Lewisian lithosphere. In this case the Archaean trace-element enrichment and element fractionation in the Lewisian lithospheric mantle sampled by the dykes was closely associated in time with the generation of the 2.9 Ga old crustal portion of the lithosphere [36,37].     

Lau Basin basalts (LBB): trace element and SrNd isotopic evidence for heterogeneity in backarc basin mantle

Diverse⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd isotopic compositions among basalts from the Lau Basin (LBB), an active backarc basin in the southwest Pacific, indicate heterogeneity in the underlying mantle. Isotopic compositions display bimodal distributions which are related to geographic location. Type I LBB (⁸⁷/Sr⁸⁶Sr 0.70366;¹⁴³Nd/¹⁴⁴Nd 0.51297) include tholeiites from the central basin, Peggy Ridge, and Rochambeau Bank, while Type II basaltic and andesitic glasses from the northeastern portion of the basin, near Niua Fo'ou island, have higher⁸⁷Sr/⁸⁶Sr ( 0.7038) and lower ¹⁴³Nd/¹⁴⁴Nd ( 0.51288). Both depleted (e.g. N-MORB) and enriched (e.g. E-MORB) trace element abundances occur among Type I and Type II LBB.Covariation between trace element and isotopic ratios among Type I LBB is consistent with mixing between depleted mantle similar to the source for MORB and relatively enriched peridotite similar to the source for E-MORB. Relative to MORB, uniformly high⁸⁷Sr/⁸⁶Sr ( +0.0005) among all Type I LBB for given Nd isotopic compositions ( ε_Nd = +8 to +12) may reflect a lithospheric component, such as ancient recycled altered ocean crust. Type II LBB have SrNd isotopic compositions which are gradational between enriched mantle similar to the source of OIB and a component with distinct Sr isotopic composition such as that observed in Samoan post-erosional basalts. Isotopic and geographic discontinuity between Type I and Type II LBB, and isotopic affinity of Type II and Niua Fo`ou island basalts with those from Samoa suggests that volcanism in the northeastern portion of the basin is tapping deeper mantle beneath the adjoining Pacific plate, as well as Indo-Australian mantle overlying the Pacific lithosphere that is subducted into the Tonga Trench.     

Pb, Nd, and Sr isotopic constraints on the origin of Miocene basaltic rocks from northeast Hokkaido, Japan: Implications for opening of the Kurile back-arc basin

Late Miocene (7–9 Ma) basaltic rocks from the Monbetsu‐Kamishihoro graben in northeast Hokkaido have chemical affinities to certain back‐arc basin basalts (referred to herein as Hokkaido BABB). Pb‐, Nd‐ and Sr‐isotopic compositions of the Hokkaido BABB and arc‐type volcanic rocks (11–13 Ma and 4–4.5 Ma) from the nearby region indicate mixing between the depleted mantle and an EM II‐like enriched component (e.g. subducted pelagic sediment) in the magma generation. At a given ⁸⁷Sr/⁸⁶Sr, Hokkaido BABB have slightly lower ¹⁴³Nd/¹⁴⁴Nd and slightly less radiogenic ²⁰⁶Pb/²⁰⁴Pb compared with associated arc‐type lavas, but both these suites are difficult to distinguish solely on the basis of isotopic compositions. These isotopic data indicate that while generation of the Hokkaido BABB involves smaller amounts of the EM II‐like enriched component than do associated arc lavas, Hokkaido BABB are isotopically distinct from basalts produced at normal back‐arc basin spreading centers. Instead, northeast Hokkaido BABB are more similar to basalts erupted during the initial rifting stage of back‐arc basins. The Monbetsu‐Kamishihoro graben may have developed in association with extension that formed the Kurile Basin, suggesting that opening of the basin continued until late Miocene (7–9 Ma).     

Petrogenetic model of the Permian Tarim Large Igneous Province

Over the last two decades great strides have been made in characterizing the spatial distribution, time sequence,geochemical characteristics, mantle sources, and magma evolution processes for various igneous rocks in the Early Permian Tarim Large Igneous Province(TLIP). This work has laid a solid foundation for revealing the evolutionary processes and genetic models of large igneous provinces(LIPs). This study systematically demonstrates the two-stage melting model for the TLIP based on our previous research work and predecessor achievements, and highlights the two types of magmatic rocks within the TLIP.The two-stage melting model suggests that the formation of the TLIP is mantle plume related. The early hot mantle plume caused the low-degree partial melting of the lithosphere mantle, while in the later stage, the plume partially melted due to adiabatic uplift and decompression. Therefore, this model carries signatures of both the "Parana" and "Deccan" models in terms of mantle plume activity. During the early stage, the mantle plume provided the heat required for partial melting of sub-continental lithosphere mantle(SCLM), similar to the "Parana Model", while later the plume acted as the main avenue for melting, as in the "Deccan Model". Basalts that erupted in the first stage have higher 87Sr/86 Sr, lower 143Nd/144 Nd ratios, and are enriched in large ion lithophile elements and high field strength elements, indicating a possible origin from the enriched continental lithosphere mantle,similar to the Parana type geochemical features. The basic-ultrabasic intrusive rocks in the second stage exhibit lower 87Sr/86 Sr,higher 143Nd/144 Nd ratios relative to the basalts, consistent with the involvement of a more depleted asthenospheric material,such as a mantle plume, similar to the Deccan type geochemical features. The first stage basalts can be further subdivided into two categories, i.e., Group 1 and Group 2 basalts. Group 2 basalts have lower 87Sr/86 Sr and higher 143Nd/144 Nd ratios than Group 1 basalts, and lie between compositions of the Group 1 basalts and second stage magmatism. Group 2 basalts may be the intermediate component of the TLIP, and the whole TLIP is the result of plume and lithosphere interaction. Developing this petrogenetic model for the TLIP aids in comprehensively understanding its magmatism and deep geological and geodynamic processes. Furthermore, this work enriches the theories describing the origin of large igneous province and mantle plume activity.     

Deccan plume,lithosphere rifting,and volcanism in Kutch,India

Kutch (northwest India) experienced lithospheric thinning due to rifting and tholeiitic and alkalic volcanism related to the Deccan Traps K/T boundary event. Alkalic lavas, containing mantle xenoliths, form plug-like bodies that are aligned along broadly east–west rift faults. The mantle xenoliths are dominantly spinel wehrlite with fewer spinel lherzolite. Wehrlites are inferred to have formed by reaction between transient carbonatite melts and lherzolite forming the lithosphere. The alkalic lavas are primitive (Mg# = 64–72) relative to the tholeiites (Mg# = 38–54), and are enriched in incompatible trace elements. Isotope and trace element compositions of the tholeiites are similar to what are believed to be the crustally contaminated Deccan tholeiites from elsewhere in India. In terms of Hf, Nd, Sr, and Pb isotope ratios, all except two alkalic basalts plot in a tight cluster that largely overlap the Indian Ridge basalts and only slightly overlap the field of Reunion lavas. This suggests that the alkalic magmas came largely from the asthenosphere mixed with Reunion-like source that welled up beneath the rifted lithosphere. The two alkalic outliers have an affinity toward Group I kimberlites and may have come from an old enriched (metasomatized) asthenosphere. We present a new model for the metasomatism and rifting of the Kutch lithosphere, and magma generation from a CO₂-rich lherzolite mantle. In this model the earliest melts are carbonatite, which locally metasomatized the lithosphere. Further partial melting of CO₂-rich lherzolite at about 2–2.5 GPa from a mixed source of asthenosphere and Reunion-like plume material produced the alkalic melts. Such melts ascended along deep lithospheric rift faults, while devolatilizing and exploding their way up through the lithosphere. Tholeiites may have been generated from the main plume head further south of Kutch.     

U-Pb isotopic geochemistry of the post-collisional mafic-ultramafic rocks from the Dabie Mountains

The U-Pb isotope geochemical study of the pyroxenite-gabbro intrusion in the Dabie Mountains shows that the post-collisional mafic-ultramafic rocks of the Dabie Mountains are characterized by relative high Pb contents, low U contents and low U/Pb ratios. These characters may be results of interaction between lithosphere or depleted asthenospheric mantle (DMM) and lower crust, but have nothing to do with mantle plume and subducted continental crust. It was first observed that some samples with lower ²⁰⁶Pb/²⁰⁴Pb and higher ²⁰⁷Pb/²⁰⁴Pb ratios show typical characters of the LOMU component. The Pb, Sr, and Nd isotopic tracing shows that three components are needed in the source of the Zhujiapu pyroxenite-gabbro intrusion. They could be old enriched sub-continental lithospheric mantle (LOMU component), lower crust and depleted asthenospheric mantle. The crust-mantle interaction process producing primitive magma of post-collisional mafic-ultramafic rocks in the Dabie Mountains could be described by a lithospheric delamination and magma underplating model. After continent-continent collision, delamination of the thickened lithosphere induced the upwelling of depleted asthenospheric mantle, which caused partial melting of asthenospheric mantle and residual sub-continental lithospheric mantle. The basaltic magma produced in this process underplated in the boundary between the crust and mantle and interacted with lower crust resulting in the geochemical characters of both enriched lithospheric mantle and lower crust.     

Formation time of the big mantle wedge beneath eastern China and a new lithospheric thinning mechanism of the North China craton—Geodynamic effects of deep recycled carbon

High-resolution P wave tomography shows that the subducting Pacific slab is stagnant in the mantle transition zone and forms a big mantle wedge beneath eastern China. The Mg isotopic investigation of large numbers of mantle-derived volcanic rocks from eastern China has revealed that carbonates carried by the subducted slab have been recycled into the upper mantle and formed carbonated peridotite overlying the mantle transition zone, which becomes the sources of various basalts. These basalts display light Mg isotopic compositions(δ26 Mg = –0.60‰ to –0.30‰) and relatively low87 Sr/86 Sr ratios(0.70314–0.70564) with ages ranging from 106 Ma to Quaternary, suggesting that their mantle source had been hybridized by recycled magnesite with minor dolomite and their initial melting occurred at 300-360 km in depth. Therefore, the carbonate metasomatism of their mantle source should have occurred at the depth larger than 360 km, which means that the subducted slab should be stagnant in the mantle transition zone forming the big mantle wedge before 106 Ma. This timing supports the rollback model of subducting slab to form the big mantle wedge. Based on high P-T experiment results, when carbonated silicate melts produced by partial melting of carbonated peridotite was raising and reached the bottom(180–120 km in depth) of cratonic lithosphere in North China, the carbonated silicate melts should have 25–18 wt% CO2 contents, with lower Si O2 and Al2 O3 contents, and higher Ca O/Al2 O3 values, similar to those of nephelinites and basanites, and have higher εNdvalues(2 to 6). The carbonatited silicate melts migrated upward and metasomatized the overlying lithospheric mantle, resulting in carbonated peridotite in the bottom of continental lithosphere beneath eastern China. As the craton lithospheric geotherm intersects the solidus of carbonated peridotite at 130 km in depth, the carbonated peridotite in the bottom of cratonic lithosphere should be partially melted, thus its physical characters are similar to the asthenosphere and it could be easily replaced by convective mantle. The newly formed carbonated silicate melts will migrate upward and metasomatize the overlying lithospheric mantle. Similarly, such metasomatism and partial melting processes repeat, and as a result the cratonic lithosphere in North China would be thinning and the carbonated silicate partial melts will be transformed to high-Si O2 alkali basalts with lower εNdvalues(to-2). As the lithospheric thinning goes on,initial melting depth of carbonated peridotite must decrease from 130 km to close 70 km, because the craton geotherm changed to approach oceanic lithosphere geotherm along with lithospheric thinning of the North China craton. Consequently, the interaction between carbonated silicate melt and cratonic lithosphere is a possible mechanism for lithosphere thinning of the North China craton during the late Cretaceous and Cenozoic. Based on the age statistics of low δ26 Mg basalts in eastern China, the lithospheric thinning processes caused by carbonated metasomatism and partial melting in eastern China are limited in a timespan from 106 to25 Ma, but increased quickly after 25 Ma. Therefore, there are two peak times for the lithospheric thinning of the North China craton: the first peak in 135-115 Ma simultaneously with the cratonic destruction, and the second peak caused by interaction between carbonated silicate melt and lithosphere mainly after 25 Ma. The later decreased the lithospheric thickness to about70 km in the eastern part of North China craton.     

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.     

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.     

Nd and Sr isotope ratios and rare earth element abundances in Reykjanes Peninsula basalts evidence for mantle heterogeneity beneath Iceland

Post-glacial tholeiitic basalts from the western Reykjanes Peninsula range from picrite basalts (oldest) to olivine tholeiites to tholeiites (youngest). In this sequence there are large systematic variations in rare earth element (REE) abundances (La/Sm normalized to chondrites ranges from 0.33 in the picrite basalts to 1.25 in the fissure tholeiites) and corresponding variations in ¹⁴³Nd/¹⁴⁴Nd (0.51317 in the picrite basalts to 0.51299 in the fissure tholeiites). The large viaration in ¹⁴³Nd/¹⁴⁴Nd, more than one-third the total range observed in most ocean islands and mid-ocean ridge basalts (MORB), is accompanied by only a small variation in ⁸⁷Sr/⁸⁶Sr (0.7031–0.7032). These ⁸⁷Sr/⁸⁶Sr ratios are within the range of other Icelandic tholeiites, and distinct from those of MORB.We conclude that the mantle beneath the Reykjanes Peninsula is heterogeneous with respect to relative REE abundances and ¹⁴³Nd/¹⁴⁴Nd ratios. On a time-averaged basis all parts of this mantle show evidence of relative depletion in light REE. Though parts of this mantle have REE abundances and Nd isotope ratios similar to the mantle source of “normal” MORB, ⁸⁷Sr/⁸⁶Sr is distinctly higher. Unlike previous studies we find no evidence for chondritic relative REE abundances in the mantle beneath the Reykjanes Peninsula; in fact, the data require significant chemical heterogeneity in the hypothesized mantle plume beneath Iceland, as well as lateral mantle heterogeneity from the Reykjanes Ridge to the Reykjanes Peninsula. The compositional range of the Reykjanes Peninsula basalts is consistent with mixing of magmas produced by different degrees of melting in different parts of the heterogeneous mantle source beneath the Reykjanes Peninsula.     

Characteristics of the mantle source region of sodium lamprophyres and petrogenetic tectonic setting in northeastern Hunan,China

~~Characteristics of the mantle source region of sodium lamprophyres and petrogenetic tectonic setting in northeastern Hunan,China~~     

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.     

Diapirism of depleted peridotite — a model for the origin of hot spots

A model is proposed for the origin of hot spots that depends on the existence of major-element heterogeneities in the mantle. Generation of basaltic crust at spreading centers produces a layer of residual peridotite ～20–25 km thick directly beneath the crust which is depleted in Fe/Mg, TiO₂, CaO, Al₂O₃, Na₂O and K₂O, and which has a slightly lower density than undepleted peridotite beneath it. Upon recycling of this depleted peridotite back into the deep mantle at subduction zones, it becomes gravitationally unstable, and tends to rise as diapirs through undepleted peridotite. For a density contrast of 0.05 g cm^?3, a diapir 60 km in diameter would rise at roughly 8 cm y^?1, and could transport enough heat to the base of the lithosphere to cause melting and volcanism at the surface. Hot spots are thus viewed as a passive consequence of mantle convection and fractionation at spreading centers rather than a plate-driving force.It is suggested that depleted diapirs exist with varying amounts of depletion, diameters, upward velocities and source volumes. Such variations could explain the occurrence of hot spots with widely varying lifetimes and rates of lava production. For highly depleted diapirs with very low Fe/Mg, the diapir would act as a heat source and the asthenosphere and lower lithosphere drifting across the diapir would serve as the source region of magmas erupted at the surface. For mildly depleted diapirs with Fe/Mg only slightly less than in normal undepleted mantle, the diapir could provide not only the source of heat but also most or all of the source material for the erupted magmas. The model is consistent with isotopic data that require two separate and ancient source regions for mid-ocean ridge and oceanic island basalts. The source for mid-ocean ridge basalts is considered to be material upwelling at spreading centers from the deep mantle. This material forms the oceanic lithosphere. Oceanic island basalts are considered to be derived from varying mixtures of sublithospheric and lower lithospheric material and the rising diapir itself.     

Isotope geochemistry of xenoliths from East Africa: Implications for development of mantle reservoirs and their interaction

Pb, Nd and Sr isotope analyses together with U, Pb, Sm, Nd, Rb and Sr concentrations have been obtained for separated phases of lherzolite and bulk rock mafic granulite xenoliths in Recent volcanics from Tanzania. A garnet lherzolite from the Lashaine vent has yielded the least radiogenicPb(²⁰⁶Pb/²⁰⁴Pb= 15.55) and Nd(¹⁴³Nd/¹⁴⁴Nd= 0.51127; ?_Nd⁰ = ?26.7) isotope compositions recorded so far for an ultramafic xenolith, and ⁸⁷Sr/⁸⁶Sr= 0.83604. The Pb isotope compositions of the mafic granulites are variable 15.77<²⁰⁶Pb/²⁰⁴Pb<17.50 and some show evidence for depletion of U relative to Pb up to 2.0 Ga ago. Overall the isotope results suggest that the mantle part of the continental lithosphere beneath Tanzania has components that have undergone a complex history that includes major chemical fractionations ca. 2.0 Ga ago. A phlogopite-amphibole vein from the Pello Hill sample has Sr, Nd and Pb isotope compositions similar to those of mid-ocean ridge basalts, indicating both a young emplacement age for the vein material and a source which had an isotopic signature characteristic of depleted mantle.The Sr, Nd and Pb isotope systematics of ultramafic xenoliths do not conform with those of MORB, particularly in terms of their PbSr, and NdPb relationships. In this regard they are similar to some ocean islands and could be a viable source material for some ocean island basalts at least. The mantle part of the continental lithosphere is as likely to contain recycled components derived from the continental crust as are other regions of mantle. If the mantle part of continental lithosphere is invoked as a source for ocean islands, it does not negate the possibility that substantial recycled components are involved.     

Sm-Nd isotopic evolution of chondrites

The¹⁴³Nd/¹⁴⁴Nd and¹⁴⁷Sm/¹⁴⁴Nd ratios have been measured in five chondrites and the Juvinas achondrite. The range in¹⁴³Nd/¹⁴⁴Nd for the analyzed meteorite samples is 5.3 ε-units (0.511673–0.511944) normalized to¹⁵⁰Nd/¹⁴²Nd= 0.2096. This is correlated with the variation of 4.2% in¹⁴⁷Sm/¹⁴⁴Nd (0.1920–0.2000). Much of this spread is due to small-scale heterogeneities in the chondrites and does not appear to reflect the large-scale volumetric averages. It is shown that none of the samples deviate more than 0.5 ε-units from a 4.6-AE reference isochron and define an initial¹⁴³Nd/¹⁴⁴Nd ratio at 4.6 AE of0.505828 ± 9. Insofar as there is a range of values of¹⁴⁷Sm/¹⁴⁴Nd there is no unique way of picking solar or average chondritic values. From these data we have selected a new set of self-consistent present-day reference values for CHUR (“chondritic uniform reservoir”) of (¹⁴³Nd/¹⁴⁴Nd)_CHUR⁰ = 0.511836and(¹⁴⁷Sm/¹⁴⁴Nd)_CHUR⁰ = 0.1967. The new¹⁴⁷Sm/¹⁴⁴Nd value is 1.6% higher than the previous value assigned to CHUR using the Juvinas data of Lugmair. This will cause a small but significant change in the CHUR evolution curve. Some terrestrial samples of Archean age show clear deviations from the new CHUR curve. If the CHUR curve is representative of undifferentiated mantle then it demonstrates that depleted sources were also tapped early in the Archean. Such a depleted layer may represent the early evolution of the source of present-day mid-ocean ridge basalts. There exists a variety of discrepancies with most earlier meteorite data which includes determination of all Nd isotopes and Sm/Nd ratios. These discrepancies require clarification in order to permit reliable interlaboratory comparisons. The new CHUR curve implies substantial changes in model ages for lunar rocks and thus also in the interpretation of early lunar chronology.     

Petrogenesis of the late Cretaceous K‐rich volcanic rocks from the Central Pontide orogenic belt,North Turkey

Subduction‐related volcanic rocks are widespread in the Central Pontides of Turkey, and represented by the Hamsaros volcanic succession in the Sinop area to the north. The volcanic rocks display high‐K calc‐alkaline, shoshonitic and ultra‐K affinities. ⁴⁰Ar/³⁹Ar age data indicate that the rocks occurred during the Late Cretaceous (ca 82 Ma), and the volcanic suites were coeval. Primitive mantle‐normalized trace element patterns of all the lavas are characterized by strong enrichments in large ion lithophile elements (LILE) (Rb, Ba, K, and Sr), Th, U, Pb, and light rare earth elements (LREE; La, Ce) and prominent negative Nb, Ta, and Ti anomalies, all typical of subduction‐related lavas. There is a systematic increase in the enrichment of incompatible trace elements from the high‐K calc‐alkaline lavas through the shoshonitic to the ultra‐K lavas. In addition, the shoshonitic and ultra‐K lavas have significantly higher ⁸⁷Sr/⁸⁶Sr (0.70666–0.70834) and lower ¹⁴³Nd/¹⁴⁴Nd (0.51227–0.51236) initial ratios than coexisting high‐K calc‐alkaline lavas (⁸⁷Sr/⁸⁶Sr 0.70576–0.70613, ¹⁴³Nd/¹⁴⁴Nd 0.51245–0.51253). Geochemical and isotopic data show that the shoshonitic and ultra‐K rocks cannot be derived from the high‐K calc‐alkaline suite by any shallow level differentiation process, and point to a derivation from distinct mantle sources. The shoshonitic and ultra‐K rocks were derived from metasomatic veins related to melting of recycled subducted sediments, but the high‐K calc‐alkaline rocks from a lithospheric source metasomatized by fluids from subduction zone.     

Nd and Sr isotope geochemistry of hydrous mantle nodules and their host alkali basalts: implications for local heterogeneities in metasomatically veined mantle

Nd and Sr isotopic data on pargasite Iherzolite inclusions, kaersutite megacrysts and their host alkali basalts are presented here to clarify some questions regarding isotopic equilibration during mantle metasomatism and the role of metasomatism in basalt genesis. Five alkali basalts from Nunivak Island within the Aleutian back-arc basin, have⁸⁷Sr/⁸⁶Sr ratios of 0.70251–0.70330 and¹⁴³Nd/¹⁴⁴Nd ratios of 0.51289–0.51304. On a Nd versus Sr isotope composition diagram the basalts overlap the fields of MORB and ocean island basalts. Pargasites and mica separated from hydrous nodules found in these basalts have a range in⁸⁷Sr/⁸⁶Sr of 0.70256–0.70337 but identical¹⁴³Nd/¹⁴⁴Nd ratios of 0.51302. The metasomatic fluid represented by the pargasite is in isotopic equilibrium, both for Sr and Nd, with the dry mantle as represented by diopside. Eight alkali basalts from the Ataq diatreme, South Yemen, have⁸⁷Sr/⁸⁶Sr range of 0.70335–0.70426 and¹⁴³Nd/¹⁴⁴Nd range of 0.51252–0.51305. On a Nd versus Sr isotope composition diagram the basalts from Ataq plot in two distinct fields, (1) within the field of ocean island basalts, and (2) within the range of continental rift basalts but to the left of the Nd-Sr correlation line, somewhat similar to the Skye and Oslo rift basalts. Diopside and pargasite separated from three nodules at Ataq have a more complex history than those at Nunivak. Two nodules contain pargasite and diopside with identical⁸⁷Sr/⁸⁶Sr ratios but different¹⁴³Nd/¹⁴⁴Nd ratios. A third nodule contains diopside with a¹⁴³Nd/¹⁴⁴Nd ratio similar to that of other diopsides.The Nunivak basalts are derived from a source with a time-integrated light-REE depletion, in contrast to the light-REE-enriched nature of the basanites. This is best explained by a recent metasomatic event in the source region which increased the LIL element content of the peridotite thus accommodating higher degrees of melting. The Ataq volcanic rocks seem to tap different sources characterized by both light-REE enrichment and depletion, in contrast to the uniform source of the Nunivak basanites. Production of the Ataq basanites is believed to involve anataxis of metasomatically veined continental mantle where local mantle heterogeneities survived the melting event.     

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.     

Lithospheric contributions to high-MgO basanites from the Cumbre Vieja Volcano,La Palma,Canary Islands and evidence for temporal variation in plume influence

New geochemical and isotopic data are presented from the oldest part of the Cumbre Vieja volcano, La Palma (Canary Islands), located near the assumed emergence of the Canary mantle plume. The volcanics comprise a suite dominated by basanite flows with subordinate amounts of phono-tephrite, tephri-phonolite and phonolite flows and intrusives. Two compositionally different basanite groups have been identified, both with HIMU (high-μ)-type incompatible trace element characteristics: Primitive high-MgO basanites (10.7–12.1% MgO), found only at the base of a stratigraphic profile near Fuencaliente on the south coast, and intermediate-MgO basanites (6.0–7.3% MgO), exposed in the upper part of the profile and widespread on the east coast of La Palma. The high-MgO basanites are interpreted as near-primary mantle melts (primary composition 14–15% MgO) derived by progressive melting (2.9% to 4.5%) of a common lithospheric mantle source. Model calculations indicate that it is not possible to generate the intermediate-MgO basanites from the high-MgO group by crystal fractionation of observed phenocrysts. Relative to intermediate-MgO basanites, the high-MgO flows have lower concentrations of LIL and HFS elements, except for Ti, which is markedly enriched in the primitive rocks (3.7–4.7% TiO₂ vs 3.4–3.9% TiO₂). Fuencaliente volcanics display limited temporal isotopic variations suggested to be a result of mixing of melts originating from the rising plume and the metazomatized lithospheric mantle. ⁸⁷Sr / ⁸⁶Sr and ¹⁴³Nd / ¹⁴⁴Nd ratios range 0.70305–0.70311 and 0.51285–0.51291, respectively, while the corresponding ranges in Pb-isotope ratios are ²⁰⁶Pb / ²⁰⁴Pb = 19.46–19.64, ²⁰⁷Pb / ²⁰⁴Pb = 15.55–15.61, and ²⁰⁸Pb / ²⁰⁴Pb = 39.16–39.53. The overall variation of the Cumbre Vieja isotopic data can be accounted for by mixtures of three mantle components in the proportions 72–79% plume source (LVC = low velocity component), 9–16% depleted mantle (DM) and up to 12% enriched mantle (EMI). Negative Δ7 / 4 Pb (− 0.6 to − 5.4) in the Cumbre Vieja volcanics suggest derivation from a young HIMU mantle source. The relative abundance of plume source material increase in younger rocks in the Fuencaliente section, suggesting waning plume–lithosphere interaction during the emplacement of this part of the Cumbre Vieja volcano. The high-MgO volcanics define regular and systematic geochemical trends, interpreted as partial melting trends, when plotted against abundances of highly incompatible elements (P, Ce). Evaluation of minor and trace element variation in consecutive melts suggests control by residual amphibole, phlogopite, garnet and a Ti-bearing phase, possibly ilmenite. The melting mode changed gradually, allowing increasing input from residual phlogopite during partial melting. The residual mineralogy constrains the source region of the high-MgO basanites to the lowermost oceanic lithospheric mantle, presumably around 100 km depths.     

Nd-Sr systematics of the Setouchi volcanic rocks,southwest Japan: a clue to the origin of orogenic andesite

Twenty-three volcanic rocks from the Setouchi volcanic belt, southwest Japan, were analyzed for Nd and Sr isotopic compositions for the purpose of examining the genetic relationships among the basalt, high-magnesium andesite (HMA) and evolved porphyritic andesite. The andesites have higher⁸⁷Sr/⁸⁶Sr (0.70487–0.70537) and lower¹⁴³Nd/¹⁴⁴Nd (0.512509–0.512731) than the basalts, i.e., 0.70408–0.70468 and 0.512691–0.512830, respectively. This result confirms earlier conclusions obtained from petrologic study that the andesites cannot be fractionation products of basaltic magma but that the andesitic and basaltic magmas were generated independently. On the basis of melting experiments for HMA and basalt, it is inferred that there is an isotopically stratified mantle beneath southwest Japan. Evolved porphyritic andesites have essentially identical Sr and Nd isotopic ratios to HMA and can be derived by fractionation of primary andesitic magma. A model to produce orogenic andesite is proposed on petrologic, experimental and isotopic bases.