Indian Ocean-MORB-type isotopic signature of Yushigou ophiolite in North Qilian Mountains and its implications

Many researchers have focused on the tectonic evolution of North Qilian Mountains (NQM) since the 1970s[1―7]. However, the tectonic affinity of the an- cient oceanic mantle in early Paleozoic remains in de-bate. Three general explanations for it have been pro- posed. The first one suggests that the ancient ocean was a part of Proto-Tethys, and the tectonic evolution of NQM should be regarded as a portion of the562 Science in China: Series D Earth Sciences Tethyan tectonic domain[1]. …     

Geochemistry of basalts from central and southern New Hebrides arc: implication for their source rock composition

The basaltic rocks from the central and southern islands of the New Hebrides-Aneityum, Tanna, Erromango, Efate, Emae, Tongoa and Epi, have geochemical features typical of island arc volcanics. They are enriched in LILE and depleted in Zr, Hf, Nb and Ta compared to N-type MORB. The rocks were derived from a similar upper mantle source as N-type MORB but with a higher degree of partial melting. In addition their source was enriched in LILE (K, Rb, Sr, Ba and LREE) probably by migrating hydrous fluids released during the dehydration of the subducted oceanic slab. The basalts from Futuna island which is located farther from the trench, display characteristics typical of calc-alkaline rocks. The Futuna basalts were generated from a different LILE-enriched upper mantle source. It seems that this upper mantle source was modified by interaction with partial melts from the subducted oceanic lithosphere.     

The subcontinental versus suboceanic debate,I Lead-neodymium-strontium isotopes in primary alkali basalts from a shield area the Ahaggar volcanic suite

Pb, Nd and Sr isotopic compositions have been determined in lherzolite-xenolith-bearing alkali-basalts from the center of the African shield. The present data are very similar to those reported for ocean-island basalts and do not support the hypothesis of different mantle sources for alkali-basalts from continental and oceanic areas. From these observations and on the basis of data obtained for xenolith in kimberlite and for tholeiitic continental basalts one may infer the following terrestrial mantle structure: whereas oceanic tholeiites would originate in upper oceanic mantle, oceanic and continental alkali basalts would come from the lower mantle and tholeiitic continental basalts from the continental lithosphere.     

A major change in magma sources in late Mesozoic active margin of the circum-Sea of Japan domain: Geochemical constraints from late Paleozoic to Paleogene mafic dykes in the Sergeevka belt,southern Primorye,Russia

More than 30 mafic dykes crop out in the Sergeevka belt in the coastal South Primorye, Far East Russia, of which geologic settings have been unclear for years. This study conducted major- and trace elements characterization, Sr–Nd isotope analyses, and Ar–Ar amphibole and U–Pb zircon datings for these rocks in order to identify their origin. The results demonstrated that all dykes are characterized by high Ba/Yb and low Nb/Y, Zr/Y, and Th/Yb ratios, which suggest their origin from arc melts derived from thin wedge mantle and shallow-dipping slab. These dykes are clearly separated into two distinct age/geochemistry suites; that is, the Paleogene and Early Cretaceous one with dolerites/basalts and adakitic rocks, and the Permian–Triassic one with high-Mg and high-Al gabbro-dolerite varieties. Their geochemistry suggests that the older suite was sourced from a primitive depleted MORB mantle (DMM)-type mantle, whereas the younger suite from an enriched mantle II (EM2)-type mantle domain. The transition in source type from DMM to EM2 occurred during the Jurassic-earliest Cretaceous time, probably by a strong influence of a mantle plume onto the long-continuing subduction-related magmatism. The plume influence reached the maximum when the unique meimechite-picrite complex formed in the region.     

Major- and trace-element systematics and isotope geochemistry of Cenozoic mafic volcanic rocks from the Vogelsberg (central Germany): Constraints on the origin of continental alkaline and tholeiitic basalts and their mantle sources

The Cenozoic basaltic province of the Vogelsberg area (central Germany) is mainly composed of intercalated olivine to quartz tholeiites and near-primary nephelinites to basanites. The inferred mantle source for the alkaline and tholeiitic rocks is asthenospheric metasomatized garnet peridotite containing some amphibole as the main hydrous phase. Trace element modelling indicates 2 to 3% partial melting for the alkaline rocks and 5 to 7% partial melting for the olivine tholeiites. Incompatible trace element abundances and ratios as well as Nd and Sr radiogenic isotope compositions lie between plume compositions and enriched mantle compositions and are similar to those measured in Ocean Island Basalts (OIB) and the Central European Volcanic Province elsewhere. The mafic olivine tholeiites have similar Ba/Nb, Ba/La and Nd–Sr isotope ratios to the alkaline rocks indicating derivation of both magma types from chemically comparable mantle sources. However, Zr/Nb ratios are slightly higher in olivine tholeiites than in basanites reflecting some fractionation of Zr relative to Nb during partial melting. Quartz tholeiites have higher Ba/Nb, Zr/Nb, La/Nb, but lower Ce/Pb ratios and lower Nd isotope compositions than the alkaline rocks which can be explained by interaction of the basaltic melt with lower (granulite facies) crustal material or partial melts thereof during stagnation within the lower crust. It appears most likely that upwelling of hot, asthenospheric material results in the generation of primitive alkaline rocks at the base of the lithosphere at depths of 75–90 km. Lithospheric extension together with minor plume activity and probably lower lithosphere erosion induced melting of shallower heterogenous upper mantle generating a spectrum of olivine tholeiitic melts. These olivine tholeiitic rocks evolved via crystal fractionation and probably limited contamination to quartz tholeiites.     

Correlated Nd,Sr and Pb isotope variation in Walvis Ridge basalts and implications for the evolution of their mantle source

Basement intersected in DSDP holes 525A, 528 and 527 on the Walvis Ridge consists of submarine basalt flows and pillows with minor intercalated sediments. These holes are situated on the crest and mid and lower northwest flank of a NNW-SSE-trending ridge block which would have closely paralleled the paleo mid-ocean ridge [13, 14]. The basalts were erupted approximately 70 m.y. ago, an age equivalent to that of immediately adjacent oceanic crust in the Angola Basin and consistent with formation at the paleo mid-ocean ridge [14]. The basalt types vary from aphyric quartz tholeiites on the ridge crest to highly plagioclase phyric olivine tholeiites on the ridge flank. These show systematic differences in incompatible trace element and isotopic composition. Many element and isotope ratio pairs form systematic trends with the ridge crest basalts at one end and the highly phyric ridge flank basalts at the other.The low ¹⁴³Nd/¹⁴⁴Nd (0.51238), ²⁰⁶Pb/²⁰⁴Pb (17.54), ²⁰⁸Pb/²⁰⁴Pb (15.47), ²⁰⁸Pb/²⁰⁴Pb (38.14) and high⁸⁷Sr/⁸⁶Sr (0.70512) ratios of the ridge crest basalts suggest derivation from an old Nd/Sm-, Rb/Sr- and Pb/U-enriched mantle source. This isotopic signature is similar to that of alkaline basalts on Tristan de Cunha but offset to significantly lower Nd and Pb isotopic ratios. The isotopic ratio trends may be extrapolated beyond the ridge flank basalts with higher¹⁴³Nd/¹⁴⁴Nd (0.51270), ²⁰⁶Pb/²⁰⁴Pb (18.32), ²⁰⁷Pb/²⁰⁴Pb (15.52), ²⁰⁸Pb/²⁰⁴Pb (38.77) and lower ⁸⁷Sr/⁸⁶Sr (0.70417) ratios in the direction of increasingly Nd/Sm-, Rb/Sr- and Pb/U-depleted source compositions. These isotopic correlations are equally consistent with mixing od depleted and enriched end member melts or partial melting of an inhomogenous, variably enriched mantle source. However, observe ZrBaNbY interelement relationships are inconsistent with any simple two-component model of magma mixing, as might result from the rise of a lower mantle plume through the upper mantle. Incompatible element and Pb isotopic systematics also preclude extensive involvement of depleted (N-type) MORB material or its mantle sources. In our preferred petrogenetic model the Walvis Ridge basalts were derived by partial melting of mantle similar to an enriched (E-type) MORB source which had become heterogeneous on a small scale due to the introduction of small-volume melts and metasomatic fluids.     

Enrichment of the continental lithosphere by OIB melts: Isotopic evidence from the volcanic province of northern Tanzania

Alkali basalts and nephelinites from the southern end of the East African Rift (EAR) in northern Tanzania have incompatible trace element compositions that are similar to those of ocean island basalts (OIB). They define a considerable range of Sr, Nd and Pb isotopic compositions (⁸⁷Sr/⁸⁶Sr= 0.7035−0.7058,ε_Nd = −5to+3, and²⁰⁶Pb/²⁰⁴Pb= 17.5−21.3), each of which partially overlaps the range found in OIB. However, they occupy a unique position in combined Nd, Sr and Pb isotopic compositional space. Nearly all of the lavas have radiogenic Pb, similar to HIMU with high time-integrated²³⁸U/²⁰⁴Pb coupled with unradiogenic Nd (+2 to −5) and radiogenic Sr (>0.704), similar to EMI. This combination has not been observed in OIB and provides evidence that these magmas predominantly acquired their Sr, Nd and Pb in the subcontinental lithospheric mantle rather than in the convecting asthenosphere. These data contrast with compositions for lavas from farther north in the EAR. The Pb isotopic compositions of basalts along the EAR are increasingly radiogenic from north to south, indicating a fundamental change to sources with higher time-integratedU/Pb, closer to the older cratons in the south. An ancient underplated OIB melt component, isolated for about 2 Ga as enriched lithospheric mantle and then remelted, could generate both the trace element and isotopic data measured in the Tanzanian samples. Whereas the radiogenic Pb in Tanzanian lavas requires a source with high time-integratedU/Pb, most continental basalts that are thought to have interacted with the continental lithospheric mantle have unradiogenic Pb, requiring a source with a history of lowU/Pb. Such lowU/Pb is readily accomplished with the addition of subduction-derived components, since the lower averageU/Pb of arc basalts (0.15) relative to OIB (0.36) probably reflects addition of Pb from subducted oceanic crust. If the subcontinental lithosphere is normally characterized by low time-integratedU/Pb it would appear that subduction magmatism is more important than OIB additions in supplying the Pb inventory of the lithospheric mantle. However,U/Pb ratios of xenoliths derived from the continental lithospheric mantle suggest that both processes may be important. This apparent discrepancy could be because xenoliths are not volumetrically representative of the subcontinental lithospheric mantle, or, more likely, that continental lithospheric mantle components in basalts are normally only identified as such when the isotopic ratios are dissimilar from MORB or OIB. Lithospheric enrichment from subaccreted OIB components appears to be more significant than generally recognized.     

U-Pb isotopic geochemistry of the post-collisional mafic-ultramafic rocks from the Dabie Mountains——Crust-mantle interaction and LOMU component

Geochronological studies of mafic-ultramafic intrusions occurrence in the northern Dabie zone (NDZ) suggest that these pyroxenite-gabbro intrusions formed 120—130 Ma ago should be post-collisional magmatic rocks[1—4]. These mafic-ultramafic rocks provid…     

Origin of Icelandic basalts: A review of their petrology and geochemistry

The petrology and geochemistry of Icelandic basalts have been studied for more than a century. The results reveal that the Holocene basalts belong to three magma series: two sub-alkaline series (tholeiitic and transitional alkaline) and an alkali one. The alkali and the transitional basalts, which occupy the off-rift volcanic zones, are enriched in incompatible trace elements compared to the tholeiites, and have more radiogenic Sr, Pb and He isotope compositions. Compared to the tholeiites, they are most likely formed by partial melting of a lithologically heterogeneous mantle with higher proportions of melts derived from recycled oceanic crust in the form of garnet pyroxenites compared to the tholeiites. The tholeiitic basalts characterise the mid-Atlantic rift zone that transects the island, and their most enriched compositions and highest primordial (least radiogenic) He isotope signature are observed close to the centre of the presumed mantle plume. High-MgO basalts are found scattered along the rift zone and probably represent partial melting of refractory mantle already depleted of initial water-rich melts. Higher mantle temperature in the centre of the Iceland mantle plume explains the combination of higher magma productivity and diluted signatures of garnet pyroxenites in basalts from Central Iceland. A crustal component, derived from altered basalts, is evident in evolved tholeiites and indeed in most basalts; however, distinguishing between contamination by the present hydrothermally altered crust, and melting of recycled oceanic crust, remains non-trivial. Constraints from radiogenic isotope ratios suggest the presence of three principal mantle components beneath Iceland: a depleted upper mantle source, enriched mantle plume, and recycled oceanic crust.The study of glass inclusions in primitive phenocrysts is still in its infancy but already shows results unattainable by other methods. Such studies reveal the existence of mantle melts with highly variable compositions, such as calcium-rich melts and a low-¹⁸O mantle component, probably recycled oceanic crust. Future high-resolution seismic studies may help to identify and reveal the relative proportions of different lithologies in the mantle.     

Siderophile and chalcophile element abundances in oceanic basalts, Pb isotope evolution and growth of the Earth''s core

We have investigated the hypothesis that mantle Pb isotope ratios reflect continued extraction of Pb into the Earth's core over geologic time. The Pb, Sr and Nd isotopic compositions, and the abundance of siderophile and chalcophile elements (W, Mo and Pb) and incompatible lithophile elements have been determined for a suite of ocean island and mid-ocean ridge basalt samples. Over the observed range in Pb isotopic compositions for oceanic rocks, we found no systematic variation of siderophile or chalcophile element abundances relative to abundances of similarly incompatible, but lithophile, elements. The high sensitivity of theMo/Pr ratio to segregation of Fe-metal or S-rich metallic liquid (sulfide) and the observed constantMo/Pr ratio rules out the core formation model as an explanation for the Pb paradox. The mantle and crust have the sameMo/Pr and the sameW/Ba ratios, suggesting that these ratios reflect the ratio in the Earth's primitive mantle.

Our data also indicate that thePb/Ce ratio of the mantle is essentially constant, but the presentPb/Ce ratio in the mantle ( 0.036) is too low to represent the primitive value ( 0.1) derived from Pb isotope systematics. HigherPb/Ce ratios in the crust balance the lowPb/Ce of the mantle, and crust and mantle appear to sum to a reasonable terrestrialPb/Ce ratio. The constancy of thePb/Ce ratio in a wide variety of oceanic magma types from diverse mantle reservoirs indicates this ratio is not fractionated by magmatic processes. This suggests crust formation must have involved non-magmatic as well as magmatic processes. Hydrothermal activity at mid-ocean ridges may result in significant non-magmatic transport of Pb from mantle to crust and of U from crust to mantle, producing a higherU/Pb ratio in the mantle than in the total crust. We suggest that the lower crust is highly depleted in U and has unradiogenic Pb isotope ratios which balance the radiogenic Pb of upper crust and upper mantle. The differences between thePb/Ce ratio in sediments, this ratio in primitive mantle, and the observed ratio in oceanic basalts preclude both sediment recycling and mixing of primitive and depleted reservoirs from being important sources of chemical heterogeneities in the mantle.     

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.     

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.     

Study on lithogeochemistry of Middle Jurassic basalts from southern China represented by the Fankeng basalts from Yongding of Fujian Province

There exists an E-W trending Middle Jurassic volcanic zone in southern China. The Fankeng basalts in the Yongding basin of Fujian Province are considered to be a typical example. The Fankeng basalts have TiO2 contents in the range of 1.92%-3.21%. They are classified as high-Ti basalts. They also have higher total Fe (averaging FeO* = 11.09%). The Middle Jurassic Fankeng basalts from southwestern Fujian have obvious distinctive lithogeochemical features from early Cre- taceous basalts from southeastern coast of China. They have higher HFSE, such as Th, Nb, Ta, Zr and Ti. Their element ratios related with HFSE, such as Zr/Ba, La/Nb, La/Ta ,Zr/Y, Ti/Y, Ba/Nb, K/Ti and Rb/Zr are similar to those of OIB. The most samples have ε Nd(T) of-0.70-0.24, which are near chondrite. Some samples have higher ε Nd(T) of 1.87-3.55.Therefore, these basaltic magmas might be derived from depleted asthenospheric mantle. The lithogeochemical characteristics of the Fankeng basalts may be caused by interaction between asthenosphere and lithosphere at the time. The (Early-) Middle Jurassic basalts and gabbros from southeastern Hunan, southern Jiangxi and northern Guangdong provinces show similar geochemical features to those of the Fankeng basalts from the Yongding of Fujian. Occurrence of these OIB-type basalts in the area may be regarded as the petrological mark of upwelling of asthenosphere at the time. Upwelling of asthenosphere has led to tectonic extension and the formation of rifted basin in the area.     

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.     

Major element, REE, and Pb, Nd and Sr isotopic geochemistry of Cenozoic volcanic rocks of eastern China: implications for their origin from suboceanic-type mantle reservoirs

Major- and rare-earth-element (REE) concentrations and UThPb, SmNd, and RbSr isotope systematics are reported for Cenozoic volcanic rocks from northeastern and eastern China. These volcanic rocks, characteristically lacking the calc-alkaline suite of orogenic belts, were emplaced in a rift system which formed in response to the subduction of the western Pacific plate beneath the eastern Asiatic continental margin. The rocks sampled range from basanite and alkali olivine basalt, through olivine tholeiite and quartz tholeiite, to potassic basalts, alkali trachytes, pantellerite, and limburgite. These rock suites represent the volcanic centers of Datong, Hanobar, Kuandian, Changbaishan and Wudalianchi in northeastern China, and Mingxi in the Fujian Province of eastern China.The major-element and REE geochemistry is characteristic of each volcanic suite broadly evolving through cogenetic magmatic processes. Some of the outstanding features of the isotopic correlation arrays are as follows: (1) NdSr shows an anticorrelation within the field of ocean island basalts, extending from the MORB end-member to an enriched, time-averaged high Rb/Sr and Nd/Sr end-member (EM1), (2) SrPb also shows an anticorrelation, similar to that of Hawaiian and walvis Ridge basalts, (3) NdPb shows a positive correlation, and (4) the ²⁰⁷Pb/²⁰⁴Pb vs ²⁰⁶Pb/²⁰⁴Pb plot shows linear arrays parallel to the general trend (NHRL) for MORB on both sides of the geochron, although in the ²⁰⁸Pb/²⁰⁴Pb vs ²⁰⁶Pb/²⁰⁴Pb plot the linear array is significantly displaced above the NHRL in a pattern similar to that of the oceanic island basalts that show the Dupal signatures. In all isotope correlation patterns, the data arrays define two different mantle components—a MORB-like component and an enriched mantle component. The isotopic data presented here clearly demonstrate the existence of Dupal compositions in the sources of the continental volcanic rocks of eastern China. We suggest that the subcontinental mantle beneath eastern China served as the reservoir for the EMI component, and that the MORB component was either introduced by subduction of the Kula-Pacific Ridge beneath the Asiatic plate in the Late Cretaceous, as proposed by Uyeda and Miyashiro, or by upwellings in the subcontinental asthenosphere due to subduction.     

Chemical differentiation of the Earth: the relationship between mantle, continental crust, and oceanic crust

The average chemical compositions of the continental crust and the oceanic crust (represented by MORB), normalized to primitive mantle values and plotted as functions of the apparent bulk partition coefficient of each element, form surprisingly simple, complementary concentration patterns. In the continental crust, the maximum concentrations are on the order of 50 to 100 times the primitive-mantle values, and these are attained by the most highly incompatible elements Cs, Rb, Ba, and Th. In the average oceanic crust, the maximum concentrations are only about 10 times the primitive mantle values, and they are attained by the moderately incompatible elements Na, Ti, Zr, Hf, Y and the intermediate to heavy REE.This relationship is explained by a simple, two-stage model of extracting first continental and then oceanic crust from the initially primitive mantle. This model reproduces the characteristic concentration maximum in MORB. It yields quantitative constraints about the effective aggregate melt fractions extracted during both stages. These amount to about 1.5% for the continental crust and about 8–10% for the oceanic crust.The comparatively low degrees of melting inferred for average MORB are consistent with the correlation of Na₂O concentration with depth of extrusion [1], and with the normalized concentrations of Ca, Sc, and Al ( 3) in MORB, which are much lower than those of Zr, Hf, and the HREE ( 10). Ca, Al and Sc are compatible with clinopyroxene and are preferentially retained in the residual mantle by this mineral. This is possible only if the aggregate melt fraction is low enough for the clinopyroxene not to be consumed.A sequence of increasing compatibility of lithophile elements may be defined in two independent ways: (1) the order of decreasing normalized concentrations in the continental crust; or (2) by concentration correlations in oceanic basalts. The results are surprisingly similar except for Nb, Ta, and Pb, which yield inconsistent bulk partition coefficients as well as anomalous concentrations and standard deviations.The anomalies can be explained if Nb and Ta have relatively large partition coefficients during continental crust production and smaller coefficients during oceanic crust production. In contrast, Pb has a very small coefficient during continental crust production and a larger coefficient during oceanic crust production. This is the reason why these elements are useful in geochemical discrimination diagrams for distinguishing MORB and OIB on the one hand from island arc and most intracontinental volcanics on the other.The results are consistent with the crust-mantle differentiation model proposed previously [2]. Nb and Ta are preferentially retained and enriched in the residual mantle during formation of continental crust. After separation of the bulk of the continental crust, the residual portion of the mantle was rehomogenized, and the present-day internal heterogeneities between MORB and OIB sources were generated subsequently by processes involving only oceanic crust and mantle. During this second stage, Nb and Ta are highly incompatible, and their abundances are anomalously high in both OIB and MORB.The anomalous behavior of Pb causes the so-called “lead paradox”, namely the elevated U/Pb and Th/Pb ratios (inferred from Pb isotopes) in the present-day, depleted mantle, even though U and Th are more incompatible than Pb in oceanic basalts. This is explained if Pb is in fact more incompatible than U and Th during formation of the continental crust, and less incompatible than U and Th during formation of oceanic crust.     

Sr isotopic composition of Afar volcanics and its implication for mantle evolution

Investigations of Rb-Sr systematics of basalts from the Afar depression (Ethiopia) indicate the presence of a heterogeneous mantle source region. The Sr isotopic compositions of the basalts from the Afar axial and transverse ranges identify source regions which are enriched in LIL elements and radiogenic Sr (axial ranges) and others which are relatively depleted (transverse ranges). Sr isotopic composition of basalts from the Red Sea, Gulf of Aden and Gulf of Tadjoura, which range from 0.70300 to 0.70340 are also reported and compared with the more radiogenic Afar region, which is characterized by⁸⁷Sr/⁸⁶Sr ranging from 0.70328 to 0.70410.Available geochemical and isotopic data suggest that a relation exists between magma composition and the advancement of the rifting process through progressive lithosphere attenuation leading to continental break-up. However, the petrogenetic process is not simple and probably implies a vertically zoned mantle beneath the Afar region. Sr isotopic evidence suggests that the vertically zoned mantle is more radiogenic and enriched in LIL elements in its upper part.     

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.     

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).     

Geochemistry of black shale at the bottom of the Lower Cambrian in Tarim Basin and its significance for lithosphere evolution

At the bottom of the Lower Cambrian, there widely develops a suit of rock association com-posed of black shales interbedded with thin silicalite in the India, northern Pakistan, Iran, southern France, England, northern Oman, the former USSR, southern Kaza…