Neodymium isotopic variations in seawater

New data for the direct measurement of the isotopic composition of neodymium in Atlantic Ocean seawater are compared with previous measurements of Pacific Ocean seawater and ferromanganese sediments from major ocean basins. Data for Atlantic seawater are in excellent agreement with Nd isotopic measurements made on Atlantic ferromanganese sediments and are distinctly different from the observed compositions of Pacific samples. These results clearly demonstrate the existence of distinctive differences in the isotopic composition of Nd in the waters of the major ocean basins and are characteristic of the ocean basin sampled. The average ε_Nd(0) values for the major oceans as determined by data from seawater and ferromanganese sediments are as follows: Atlantic Ocean,ε_Nd(0) ? ?12 ± 2; Indian Ocean,ε_Nd(0) ? ?8 ± 2; Pacific Ocean,ε_Nd(0) ? ?3 ± 2. These values are considerably less than ε_Nd(0) value sources with oceanic mantle affinities indicating that the REE in the oceans are dominated by continental sources. The difference in the absolute abundance of¹⁴³Nd between the Pacific and Atlantic Oceans corresponds to ～10⁶ atoms¹⁴³Nd per gram of seawater. The correspondence between the¹⁴³Nd/¹⁴⁴Nd in seawater and in the associated sediments suggests the possible application of this approach to paleo-oceanography.Distinctive differences in ε_Nd(0) values are observed in the Atlantic Ocean between deep-ocean water associated with North Atlantic Deep Water and near-surface water. This suggests that North Atlantic Deep Water may be relatively well mixed with respect to Nd isotopic composition whereas near-surface water may be quite heterogeneous, reflecting different sources for surface waters relative to deep water. This suggests that it may be possible to distinguish the sources of water masses within an ocean basin on the basis of Nd isotopic composition.The Nd isotopic variations in seawater are used to relate the residence time of Nd and mixing rates between the oceans.     

Nd and Sr isotopic variations in Chinese eolian deposits during the past 8 Ma: Implications for provenance change

A record of changes in Nd and Sr isotopic composition of the eolian deposits from the central Loess Plateau has been determined for the past 8 Ma. The isotopic records of the silicate fraction of the Quaternary and Tertiary eolian deposits allow interpreting the interplay between the Sr isotopic variations in the eolian deposits and the late Cenozoic tectonic and climatic changes. The results indicate that the temporal variations of Nd and Sr isotopes show remarkable changes around the beginning of the Quaternary. The lower values of the ¹⁴³Nd/¹⁴⁴Nd and the decreasing trend of the ⁸⁷Sr/⁸⁶Sr ratios after 2.58 Ma ago are attributed to the additions of relatively younger crust materials in response to the climatic cooling and the late Cenozoic uplift induced glacial grinding in the high orogenic belts in central Asia. In this context, the substantial changes in climate and tectonics have modified dust sources significantly, and the Quaternary loess forming processes are preferentially sampling relatively younger and high relief crust materials than that of the Tertiary Red Clay.     

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

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

Nd and Sr isotopic variations of Early Paleozoic oceans

We report¹⁴³Nd/¹⁴⁴Nd and⁸⁷Sr/⁸⁶Sr isotopic data for Lower Paleozoic phosphatic brachiopod and conodont fossils. The data appear to represent the isotopic values of Early Paleozoic seawaters. We show that different paleoceanic water masses can be distinguished on the basis of their ε_Nd signatures. Two sides of what is classically considered one circulating Iapetus Ocean have different ε_Nd signatures from at least the Middle Cambrian until the Late Middle Ordovician. We infer two ocean basins between North America and Baltica separated by an island and/or shoal circulation barrier. Thus, it appears necessary to redefine the area of the Iapetus Ocean. The ε_Nd signature of the redefined smaller Iapetus Ocean ranges from −5 to −9 and the ε_Nd signature of the larger, coeval Panthalassa Ocean, including part of what was formerly called the Iapetus Ocean, ranges from −10 to −20. The first time that the ε_Nd values are identical in these two water masses is coincident with the onset of the Taconic Orogeny of North America. The paleogeographic geometry we infer from this work is consistent with paleogeographic reconstructions having the Baltica continent at very high latitudes in the Early/Middle Ordovician. The ε_Nd and faunal distribution support temperature-controlled conodont faunal provinciality. A rough mean age for exposed continental crust in the Early Paleozoic can be obtained from the average ε_Nd value of Early Paleozoic Oceans. The data suggest that the mean age of the crust as a function of time has remained essentially constant or even decreased during the past 500 Ma, and suggest substantial additions of new crust to the continents through the Phanerozoic.     

The provenance of Gansu Group in Longxi region and implications for tectonics and paleoclimate

The Neogene sediments of Gansu Group from northwestern China contain eolian and fluvial deposits.The origins of these sediments are very important for exploring the onset of Asian inland aridification,the pattern of paleo-atmospheric circulation,and the regional tectonics and geomorphic evolution during the Miocene.Here we present detrital-zircon age spectra of typical eolian and fluvial deposits from highlands and subsidence basin,and compare them with those of surrounding eroded mountain(such as the West Qinling Mountains and Liupan Mountains)materials and Quaternary loess derived from the Asian inlands.The results reveal that(1)the detrital-zircon age spectrum of the Miocene eolian sample is remarkably different from the eroded materials of the West Qinling Mountains and the Miocene fluvial deposits from Tianshui region,but very similar to the Quaternary loess deposits.This indicates that the provenance of Miocene eolian sediments is similar with the Quaternary loess,and thus further confirms the previous conclusions that the distribution of Asian arid lands and the pattern of atmospheric circulation during the Miocene are broadly similar with the Quaternary.(2)The detrital-zircon age spectrum of the fluvial deposits(with age about 11.5 Ma)from Tianshui region is different from the eroded materials of West Qinling Mountains,but similar with that of the Liupan Mountains to the east,which may suggest that the Liupan Mountains have already been exhumed by11.5 Ma.     

Numerical models for diagenesis and the Neogene Sr isotopic evolution of seawater from DSDP Site 590B

A numerical model for the diagenetic exchange of Sr between carbonates and their pore fluids during sedimentation and compaction has been developed. The model has been applied to data from DSDP Site 590B in order to assess the accuracy with which the Sr isotope record in the carbonate sediment reflects that of seawater. The most important process affecting the Sr in the solid carbonate is exchange with the pore fluid due to solution-reprecipitation, but the concentration or isotopic composition of Sr in the solid itself gives little or no information as to the magnitude of this exchange. The key to determining the rate of exchange is the pore fluid, where the variations of Sr²⁺ and⁸⁷Sr/⁸⁶Sr with depth are very sensitive indicators. The logical structure of applying the model to data from DSDP 590B is to find by successive iteration an ocean history (i.e., the initial⁸⁷Sr/⁸⁶Sr and Sr concentration of each increment of carbonate deposited) and a rate of Sr exchange between pore water and solid carbonate such that the model matches the present Sr concentration and⁸⁷Sr/⁸⁶Sr of both pore water and solid carbonate.Once all the data are matched, the model provides an estimate of the rate of Sr exchange due to solution-reprecipitation and the evolution of⁸⁷Sr/⁸⁶Sr in seawater over the past 20 million years. For DSDP 590B we find that solution-reprecipitation decreases rapidly with depth, from a near surface value of about 10% per million years to about 1% per million years below 200 m. This rate of exchange of Sr results in the carbonates of DSDP 590B preserving an accurate record of the Sr isotopic evolution of the ocean over the past 5 million years, but for ages greater than 5 million years the⁸⁷Sr/⁸⁶Sr ratio of the carbonate is systematically displaced from that of the seawater in which it was deposited. The maximum difference is of order 5 × 10⁻⁵.     

Diagenesis and Sr isotopic evolution of seawater using data from DSDP 590B and 575

New Sr isotopic and concentration analyses of bulk carbonate and porewaters from a carbonate-rich Miocene section sampled at DSDP Site 575 are reported and used, along with our earlier data from a section of similar age at DSDP Site 590B, in a numerical model to determine for each site the rate of Sr exchange during diagenesis and the degree to which this amount of exchange has shifted the⁸⁷Sr⁸⁶Sr of the bulk carbonate from the ratio each increment of sediment had when first deposited. Despite the fact that the two sites have very different water depth (4536 m at 575 vs. 1299 m at 590B), different sedimentation rate ( 10 m/My at 575 vs. 40 m/My at 590B), and significantly different porewater Sr²⁺ gradients, we find that the rate of Sr exchange as a function of sediment age is almost indistinguishable between the two sites. The rate of Sr exchange determined at the two sites is such that the resulting shift in bulk carbonate⁸⁷Sr⁸⁶Sr due to diagenesis is small compared to the total range of⁸⁷Sr⁸⁶Sr values measured, but large compared to the analytical uncertainty of the individual isotopic ratio measurements. By taking this shift into account we reconstruct the original⁸⁷Sr⁸⁶Sr of each increment of carbonate sampled, which when plotted as a function of age becomes our best estimate of the Sr isotopic evolution of seawater. Because Sr is very well mixed in the ocean, at any given time there is a single worldwide value of seawater⁸⁷Sr⁸⁶Sr. Therefore, if we are quantitatively accounting for the effect Sr exchange, we should find the same seawater evolution curve regardless of what DSDP Site is used. When we compare the observed bulk carbonate⁸⁷Sr⁸⁶Sr vs. age at the two sites they are seen to differ by amounts that are sometimes large compared to the analytical uncertainties of the measurements. However, when these data are corrected for the post-depositional Sr isotopic shifts predicted by our diagenetic model, we find almost perfect agreement. This agreement suggests that we have made a realistic determination of the rate of Sr exchange and its consequences in terms of shifting the⁸⁷Sr⁸⁶Sr of the bulk carbonate, and more importantly, that Sr isotopes can be used to correlate marine sediments with an accuracy comparable to the very small analytical uncertainties of modern isotopic measurements.     

δO of carbonate, quartz and phosphate from belemnite guards: implications for the isotopic record of old fossils and the isotopic composition of ancient seawater

Belemnite guards of Cretaceous and Jurassic age were found to contain varying amounts of quartz deposited both on the external surface and inside the rostrum. The oxygen isotopic composition of coexisting carbonate, quartz and phosphate from the same rostrum was measured according to well-established techniques. None of these compounds showed isotopic values in equilibrium with one another. Assuming δ¹⁸O values of the diagenetic water within the range of meteoric waters, the δ¹⁸O(SiO₂) yield temperatures in agreement with the apparent secondary origin of this phase. The δ¹⁸O(CO₃²⁻) range, with a certain continuity, between −10.8 and +0.97 PDB-1 with most of the intermediate values being within the range of the carbonate isotopic values of Mesozoic fossils. The most positive isotopic results obtained from phosphate are close to +23/+24‰ (V-SMOW). They can hardly be related to a secondary origin of the phosphate, or to the presence of diagenetic effects, since these results are among the most positive ever measured on phosphate. As far as we know there is no widespread diagenetic process determining an ¹⁸O enrichment of phosphate. The very low concentration of phosphate did not allow the determination of its mineralogical composition. All the available δ¹⁸O(PO₄³⁻) values from belemnite and non-belemnite fossils of marine origin of Tertiary and Mesozoic age are reported along with the newly measured belemnites. The following conclusions may be drawn from the data reported: (1) the pristine oxygen isotope composition of fossil marine organisms (either carbonate or phosphate) may easily undergo fairly large changes because of oxygen isotope exchange processes with diagenetic water; this process is apparent even in the case of geologically recent fossils; (2) the δ¹⁸O(PO₄³⁻) of belemnite rostra seems to be, at least in the case of the most positive results, in isotopic equilibrium with environmental water because of the similarity between the results from Cretaceous belemnites and the results from Cretaceous and Lower Tertiary pelecypods and fish teeth; 3) if so, the only feasible interpretation that can be suggested for the ¹⁸O enriched data is the possibility of a relatively large variation of the oxygen isotopic composition of ocean paleowater from Jurassic to recent time.     

A 12-kyr record of microbial branched and isoprenoid tetraether index in Lake Qinghai,northeastern Qinghai-Tibet Plateau: Implications for paleoclimate reconstruction

Branched and Isoprenoid Tetraether (BIT) index was considered as a proxy for terrestrial organic matter input in lake sediments, based on the assumption that branched glycerol dialkyl glycerol tetraethers (bGDGTs) are mainly derived from terrestrial soils. However, mounting evidences have showed that the in situ production of bGDGTs is widespread in lakes, challenging BIT as a reliable terrestrial input proxy. Recently, BIT has been proven to be a reliable proxy for paleohydrology in a small crater lake (Lake Challa) in accordance with a different mechanism. However, the response of BIT to paleohydrology variation may differ for different lakes. In this study, we investigate the variations in the BIT index and the concentrations of its related GDGTs in a 12-ka sediment core from Lake Qinghai, in combination with our previous results for surface sediments. We find that variations in BIT strongly depend on the concentration of crenarchaeol in both surface and ancient sediments of this lake, whereas bGDGT concentration varies much less remarkably. Considering that crenarchaeol production is positively correlated with water depth in Lake Qinghai, water depth may exert negative control on the BIT index in this lake. This case is inconsistent with the positive relationship between BIT and lake levels or rainfall intensity reported for Lake Challa, suggesting that the response of BIT to local paleohydrology is site specific in lacustrine systems. Hence, the application of sedimentary BIT as a paleohydrological proxy in a specific lake requires caution before confirming the environmental controls on BIT in that lake.     

Extrusion and gravity current of a fluid: Implications for salt tectonics

Numerical models of the extrusion and gravity current of a viscous incompressible fluid are studied to determine the shapes of salt structures formed on the Earth’s surface and the velocities of rock salt extrusion and lateral spreading. Two main types of salt extrusion are examined. In the case of active extrusion, salt rises to the surface at a velocity of about 30–35 cm/yr, forming a salt dome about 550 m in height. In the case of passive extrusion, the velocity of salt extrusion from under a newly developing sedimentary minibasin is significantly lower. In the course of its evolution, the salt dome becomes topographically lower and transforms into a broad plateau. The extrusion velocity of salt controls the shape, size, and velocity of its gravity current. The shapes of salt domes modeled in this study agree well with observations. The gravity current velocities in the models vary from 3 m/yr to 60 cm/yr, depending on the proximity to the current orifice. Numerical modeling of salt extrusion and gravity current in various geodynamic settings can be used for a detailed analysis of the geological and geophysical evolution of structures containing salt layers and the related oil and gas fields.     

The sulfur isotopic composition of Neoproterozoic seawater sulfate: implications for a snowball Earth?

The present study employs a method for analysis of the sulfur isotopic composition of trace sulfate extracted from carbonates collected in Namibia in order to document secular variations in the sulfur isotopic composition of Neoproterozoic oceanic sulfate and to assess variations in the sulfur cycle that may have accompanied profound climatic events that have been described as the snowball Earth hypothesis. The carbonates in the Otavi Group of Northwest Namibia contain 3-295 ppm sulfate. Positive excursions, to a high of 40‰ (CDT), occur above the lower (Chuos Formation) and upper (Ghaub Formation) glacial intervals in the Rasthof and Maieberg cap carbonates, respectively. Positive excursions at the top of the Rasthof Formation (reaching 51‰) and within the overlying Gruis Formation (34‰) do not appear to correspond to glaciation. The δ³⁴S_sulfate values within the Ombaatjie Formation exhibit shifts over relatively short stratigraphic intervals (tens of meters), varying between ∼15 and 25‰. Cap carbonates from Australia exhibit positive δ³⁴S_pyrite trends with amplitudes similar to those of Namibian δ³⁴S_sulfate, although, more data are necessary to firmly establish these δ³⁴S trends as global in nature. δ³⁴S_sulfate excursions found in Namibian cap carbonates are consistent with the snowball Earth hypothesis in that they appear to reflect nearly complete reduction of sulfate in an isolated, anoxic global ocean, although, there are other mechanisms that may have facilitated these large shifts in δ³⁴S_sulfate. Regardless, the low sulfate concentrations in Otavi carbonates, the high amplitude variability of the δ³⁴S_sulfate curve, and the apparently full reduction of sulfate (as implied from δ³⁴S_pyrite data), even in strata low in C_org, suggest that Neoproterozoic oceanic sulfate concentrations were much lower than modern values. Additionally, the buildup of ferrous iron and banded-iron formations during the Sturtian glacial event would indicate that Fe supply exceeded sulfide availability during the glacials and/or that all sulfide was fixed and buried. This could be construed as further evidence in support of low oceanic sulfate (and sulfide) at this time.     

Episodic mantle differentiation: Nd and Sr isotopic evidence

Clinopyroxenes separated from two hydrous and four anhydrous ultramafic nodules, selected from a suit of xenoliths from Dreiser Weiher (DW), West Germany, have been studied for Nd and Sr isotopic composition. Nd exhibits a range of ε_JUV(T) from 0 to +12.4 and ⁸⁷Sr/⁸⁶Sr varies between 0.70185 and 0.70400. T_ICE model ages for anhydrous nodules indicate that the mantle underlying DW was originally depleted ?2 AE ago. Correlation of ¹⁴³Nd/¹⁴⁴Nd with Sm/Nd in this group of samples suggests that a second partial melting event occurred about 560 m.y. ago resulting in LREE enrichment of at least part of the anhydrous mantle. During a later episode, probably contemporaneous with the eruption of the host basalt in Quaternary times, most of the spinel peridotitic upper mantle below DW was modified. This metasomatism led to hydration and incompatible element enrichment of originally anhydrous mantle. The isotopic data for the anhydrous nodules again demonstrate that oceanic-type mantle underlies at least some continental areas. It is apparent that the separation of subcontinental mantle regions from an initially chondritic reservoir may occur in several discrete episodes. However, differing histories of depletion and/or enrichment will produce isotopically distinct mantle reservoirs. Therefore, basalts extracted from these mantle reservoirs will scatter about an average Nd-Sr trend line reflecting the nature of the differentiation in their source regions.     

The strontium isotopic composition of seawater,and seawater-oceanic crust interaction

The⁸⁷Sr/⁸⁶Sr ratio of seawater strontium (0.7091) is less than the⁸⁷Sr/⁸⁶Sr ratio of dissolved strontium delivered to the oceans by continental run-off (～0.716). Isotope exchange with strontium isotopically lighter oceanic crust during hydrothermal convection within spreading oceanic ridges can explain this observation. In quantitative terms, the current⁸⁷Sr/⁸⁶Sr ratio of seawater (0.7091) may be maintained by balancing the continental run-off flux of strontium (0.59 × 10¹² g/yr) against a hydrothermal recirculation flux of 3.6 × 10¹² g/yr, during which the⁸⁷Sr/⁸⁶Sr ratio of seawater drops by 0.0011. A concomitant mean increase in the⁸⁷Sr/⁸⁶Sr ratio of the upper 4.5 km of oceanic crust of 0.0010 (0.7029–0.7039) should be produced. This required⁸⁷Sr enrichment has been observed in hydrothermally metamorphosed ophiolitic rocks from the Troodos Massif, Cyprus.The post-Upper Cretaceous increase in the strontium isotopic composition of seawater(～0.7075–0.7091) covaries smoothly with inferred increase in land area. This suggests that during this period the main factor which has caused variability in the⁸⁷Sr/⁸⁶Sr ratio of seawater strontium could have been variation in the magnitude of the continental run-off flux caused by variation in land area. Variations in land area may themselves have been partly a consequence of variations in global mean sea-floor spreading rate.     

南海北部磁异常特征及对前新生代构造的指示

为了研究南海北部前新生代构造,利用新近的船载磁力测量数据,对磁异常进行变纬度化极,并反演计算视磁化强度和磁源重力异常,以及对三条OBS剖面进行重磁拟合.结果认为东沙隆起高磁异常带是浙闽沿海火山岩带向西的延续,其间被NW向古老的转换边界断裂F10错断;NE向的F2断裂是高磁异常带的南界,并限制了底侵活动的北界;F3断裂在拉伸减薄前是一个薄弱带,两侧深部热状态存在差异,极有可能是晚中生代古俯冲缝合带位置.磁静区在F2和F3断裂之间的磁性层磁性减弱,主要原因是底侵活动引起的热蚀变作用影响;而在F3断裂南侧磁性层磁性较强且较为破碎,斜磁化下磁异常正负相互压制是该区形成弱正磁异常的主要原因,该区磁性层的独特特征也可能反映了"古洋壳"的存在.     

The NdSr isotopic correlation in mantle materials and geodynamic consequences

The neodymium-strontium isotopic correlation observed in most of the Earth mantle materials is evaluated by means of direct modelling. Several geochemical models are quantitatively developed to explain the observations. The main results of this modelling are that such a correlation is not geochemically trivial and that it corresponds to specific conditions in chemical fractionation. These specific conditions seem to be satisfied by solid-liquid partitioning in magmatic conditions. The discussion of the experimental data supports a continuous convecting-magmatic fractionation model for a large proportion of the mantle.     

Temporal variations in Sr and 87Sr/86Sr of the Ganga headwaters: estimates of dissolved Sr flux to the mainstream

The headwaters of the Ganga (the Alaknanda, Bhagirathi and the Ganga) were analysed for their dissolved major ions, Sr and ⁸⁷Sr/⁸⁶Sr on a biweekly to monthly basis over a period of one year to determine their temporal variations and the factors contributing to them. The concentrations of major ions and Sr show significant seasonal variation with lower values during monsoon period in all the three rivers. A similar trend is also observed for ⁸⁷Sr/⁸⁶Sr and Na*/Ca (Na* = Na_r? Cl_r) suggesting relatively lower contribution of Sr and Na from silicates (which are more radiogenic in Sr) during monsoon. Budget calculations show that silicate derived dissolved Sr (Sr_s) in the river Ganga, Alaknanda and the Bhagirathi varied from 10 ± 4 to 27 ± 11, 7 ± 3 to 30 ± 12, 16 ± 6 to 57 ± 23% of measured Sr respectively with lower values during monsoon. The relative decrease in silicate erosion compared to carbonate during monsoon can result from several factors, these include higher dissolution kinetics of the carbonates, lower water–rock interaction time and availability of larger area for weathering. The annual discharge weighted Sr flux derived from the time series data is higher by ～20% from that based on peak flow Sr, and lower by ～40% compared to that derived from lean flow Sr concentration. The area‐normalized annual flux of dissolved Sr from the Ganga at Rishikesh is about five times its flux at Rajshahi (Bangladesh) and a few other major global rivers, such as the Amazon, indicating higher erosion rate over the Himalaya. Copyright © 2010 John Wiley & Sons, Ltd.     

The Shabogamo Intrusive Suite,Labrador: Sr and Nd isotopic evidence for contaminated mafic magmas in the Proterozoic

The Shabogamo Intrusive Suite comprises numerous bodies of variably metamorphosed gabbro which intrude Archean and Proterozoic sequences at the junction of the Superior, Churchill, and Grenville structural provinces in western Labrador. Combined Sm-Nd and Rb-Sr systematics in two bodies, ranging from unmetamorphosed to lightly metamorphosed, document a crystallization age of about 1375 m.y., and suggest that both bodies crystallized from magmas with similar Nd and Sr isotopic compositions. This age is in accordance with the existence of a regional magmatic event in the Churchill Province at approximately 1400 m.y.Rb-Sr systematics in two bodies of amphibolite-grade gabbro suggest a regional metamorphic event at about 950 m.y., corresponding to the waning stages of Grenville activity. Sm-Nd systematics in these high-grade bodies are affected to a much lesser degree than Rb-Sr.Initial ratios for¹⁴³Nd/¹⁴⁴Nd and⁸⁷Sr/⁸⁶Sr are lower and higher, respectively, than bulk earth values at 1375 m.y. Both these displacements are in the direction of older crustal material at 1375 m.y., and a model is proposed to produce the Shabogamo magma by mixing a mantle-derived magma with a partial melt of crustal rocks (approximately 4: 1 by volume). Young volcanic rocks with anomalous Nd and Sr isotopic ratios, which have previously been taken as evidence for “enriched” mantle, may be interpreted similarly.     

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.     

Geochemistry of high-Mg andesites from the early Cretaceous Yixian Formation, western Liaoning: Implications for lower crustal delamination and Sr/Y variations

The Yixian Formation at Sihetun in western Liao- ning Province has attracted considerable attention over the last two decades due to discovery of a wide range of well-preserved ‘feathered’ dinosaurs and primitive bird fossils[1―4]. This formation is dominated by vol- canic rocks, with fossil-bearing lacustrine sedimentary rocks at the upper part of the section[4]. The sedimen- tary rocks contain thin layers of tuff. According to previous studies[4], the total thickness of the Yixian Form…