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.     

Samarium-neodymium data on two late Proterozoic ophiolites of Saudi Arabia and implications for crustal and mantle evolution

Whole-rock and mineral samples from the Jabal al Wask and Jabal Ess ophiolites, northwestern Saudi Arabia, yield Sm-Nd isochron ages of 743+24 Ma and 782±38 Ma, respectively. These formation ages, which provide maximum limits for possible obduction ages, are in broad but not precise agreement with the previously known geologic history of the Arabian Shield. They indicate that the ophiolitic rocks are roughly coeval with nearby volcanic and plutonic rocks, supporting a back-arc origin for the two ophiolites. We suggest that the Jabal al Wask and Jabal Ess ophiolites were parts of the same northeast-southwest trending ophiolite belt, now offset along the Najd fault system. Initial _Nd values range from +6.6 to+ 7.6, indicating derivation from a mantle source that has been LIL-depleted for at least 2 Ga. Reported _Nd values from the Arabian Shield that are lower than this suggest the presence of older, reworked continental crust.     

Lead isotope relations in oceanic Ridge basalts from the Juan de Fuca-Gorda Ridge area N.E. Pacific Ocean

Lead isotopic analyses of a suite of basaltic rocks from the Juan de Fuca-Gorda Ridge and nearby seamounts confirm an isotopically heterogeneous mantle known since 1966. The process of mixing during partial melting of a heterogeneous mantle necessarily produces linear data arrays that can be interpreted as secondary isochrons. Moreover, the position of the entire lead isotope array, with respect to the geochron, requires that U/Pb and Th/Pb values are progressively increased over the age of the earth. Partial melting theory also dictates analogous behavior for the other incompatible trace elements. This process explains not only the LIL element character of MOR basalts, but also duplicates the spread of radiogenic lead data collected from alkali-rich oceanic basalts. This dynamic, open-system model of lead isotopic and chemical evolution of the mantle is believed to be the direct result of tectonic flow and convective overturn within the mantle and is compatible with geophysical models of a dynamic earth.     

Sm-Nd,K-Ar and petrologic study of some kimberlites from eastern United States and their implication for mantle evolution

We provide new data on Sm-Nd systematics, K-Ar dating and the major element chemistry of kimberlites from the eastern United States (mostly from central New York State) and their constituent mineral phases of olivine, clinopyroxene, garnet, phlogopite and perovskite. In addition, we report Nd-isotopes in a few kimberlites from South Africa, Lesotho and from the eastern part of China. The major element compositions of the New York dike rocks and of their constituent minerals including a xenolith of eclogite are comparable with those from the Kimberley area in South Africa. The K-Ar age of emplacement of the New York dikes is further established to be 143 Ma.We have analyzed the Nd-isotopic composition of the following kimberlites and related rocks: Nine kimberlite pipes from South Africa and Lesotho, two from southern India; one from the U.S.S.R., fifteen kimberlite pipes and related dike rocks from eastern and central U.S. and two pipes from the Shandong Province of eastern China. The age of emplacement of these kimberlites ranges from 1300 million years to 90 million years. The initial Nd-isotopic compositions of these kimberlitic rocks expressed as _Nd ^I with respect to a chondritic bulk-earth growth-curve show a range between 0 and +4, with the majority of the kimberlites being in the range 0 to +2. This range is not matched by any other suite of mantle-derived igneous rocks. This result strengthens our earlier conclusion that kimberlitic liquids are derived from a relatively primeval and unique mantle reservoir with a nearly chondritic Sm/Nd ratio.     

Small-scale convection under the back-arc occurring in the low viscosity wedge

Water released from subducting slabs through a dehydration reaction may lower the viscosity of the mantle significantly. Thus, we may expect a low viscosity wedge (LVW) above the subducting slabs. The LVW coupled with a large-scale flow induced by the subducting slabs may allow the existence of roll-like small-scale convection whose axis is normal to the strike of the plate boundary. Such a roll structure may explain the origin of along-arc variations of mantle temperature proposed recently in northeast Japan. We study this possibility using both 2D and 3D models with/without pressure- and temperature-dependent viscosity. 2D models without pressure and temperature dependence of viscosity show that, with a reasonable geometry of the LVW and subduction speed, small-scale convection is likely to occur when the viscosity of the LVW is less than 10¹⁹ Pa s. Corresponding 3D model studies reveal that the wavelength of rolls depends on the depth of the LVW. The inclusion of temperature-dependent viscosity requires the existence of further low viscosity in the LVW, since temperature dependence suppresses the instability of the cold thermal boundary layer. Pressure (i.e. depth) dependence coupled with temperature dependence of the viscosity promotes short wavelength instabilities. The model, which shows a relatively moderate viscosity decrease in the LVW (most of the LVW viscosity is 10¹⁸∼10¹⁹ Pa s) and a wavelength of roll ∼80 km, has a rather small activation energy and volume (∼130 kJ/mol and ∼4 cm³/mol) of the viscosity. This small activation energy and volume may be possible, if we regard them as an effective viscosity of non-linear rheology.     

Contribution of abiogenic and biogenic particles to trace-metal composition of phytoplankton assemblages in seawater of Shimizu Port, Japan

The contribution of abiogenic and biogenic particles to trace-metal (As, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Sb, Ti, V, and Zn) composition was investigated for phytoplankton (primarily diatoms) collected in Shimizu Port, a coastal seawater region. Except for Cd, the trace metals occurred predominantly in lithogenic or nonlithogenic abiogenic particles associated with plankton. In contrast, it is likely that Cd in seawater is taken up intracellularly, and not adsorbed extracellularly by phytoplankton. The lower P-normalized quotas of Cd in Shimizu Port than in offshore regions may be because plankton are dominated by diatoms.     

Characterization of Fe(III) (hydr)oxides in arsenic contaminated soil under various redox conditions by XAFS and Mössbauer spectroscopies

Characterization of Fe(III) (hydr)oxides in soils near the Ichinokawa mine was conducted using X-ray absorption fine structure (XAFS) and Mössbauer spectroscopies, and the structural changes were correlated with the release of As into pore-water. The Eh values decreased monotonically with depth. Iron is mainly present as poorly-ordered Fe(III) (hydr)oxides, such as ferrihydrite, over a wide redox range (from Eh = 360 to −140 mV). Structural details of the short-range order of these Fe(III) (hydr)oxides were examined using Mössbauer spectroscopy by comparing the soil phases with synthesized ferrihydrite samples having varying crystallinities. The crystallinity of the soil Fe (hydr)oxides decreased slightly with depth and Eh. Thus, within the redox range of this soil profile, ferrihydrite dominated, even under very reducing conditions, but the crystalline domain size, and, potentially, particle size, changed with the variation in Eh. In the soil–water system examined here, where As concentration and the As(III)/As(V) ratio in soil water increased with depth, ferrihydrite persisted and maintained or even enhanced its capacity for As retention with increased reducing conditions. Therefore, it is concluded that As release from these soils largely depends on the transformation of As(V) to As(III) rather than reductive dissolution of Fe(III) (hydr)oxide.     

U-Th-Pb and Rb-Sr systematics of Allende and U-Th-Pb systematics of Orgueil

U-Th-Pb systematics study of Allende inclusions showed that U, Th and Sr concentrations in Ca, Al (pyroxene)-rich chondrules and white and pinkish-white aggregate separates of Allende are five to ten times higher than those of the matrix, whereas Mg (olivine)-rich chondrules have U and Th concentrations about twice as high as the matrix. Th concentrations are extremely high in white aggregates and in pinkish-white (spinel-rich) aggregates while U and Sr concentrations in white aggregates are more than twice as high as those in pinkish-white aggregates. Large enrichment of these refractory elements in the white aggregates indicates that they contain high-temperature condensates from the solar nebula. The Pb concentrations in the inclusions are less than half of those in the whole rock and matrix, indicating that the matrix is a lower-temperature condensate. The isotopic composition of lead in the matrix is less radiogenic than that of the whole meteorite, whereas lead in Ca- and Al-rich chondrules and aggregates is extremely radiogenic. The ²⁰⁶Pb/²⁰⁴Pb ratio reaches as high as 55.9 in a white aggregate separate. The lead of Mg-rich chondrules is moderately radiogenic and the ²⁰⁶Pb/²⁰⁴Pb ratio ranges from 18 to 26. A striking linear relationship exists among leads in the chondrules, aggregates and matrix on the ²⁰⁷Pb/²⁰⁴Pb vs ²⁰⁴Pb/²⁰⁴Pb plot. The slope of the best fit line is 0.6188 ± 0.0016, yielding an isochron age of 4553 ± 4 m.y. The regression line passes through primordial lead values obtained from Canyon Diablo troilite. The data, when corrected for Canyon Diablo troilite Pb and plotted on a U-Pb concordia diagram, show that the pink and white aggregates and the Ca-Al-rich and Mg-rich inclusions have excess Pb and define a chord which intersects the concordia curve at 4548 ± 25 m.y. and 107 ± 70 m.y. The intercepts might correspond to the agglomeration age of the meteorite and a time of probably later disturbance, respectively. The matrix and some chondrules which contain less radiogenic lead did, however, not fit on the chord. The Rb-Sr data of Allende did not define an isochron suggesting that the Rb-Sr system was also disturbed by a later event, as suggested by the U-Pb concordia data. The lowest observed ⁸⁷Sr/⁸⁶Sr ratio in Allende inclusions is similar to the initial ratio of the Angra dos Reis achondrite (Papanastassiou, Thesis, 1970).The initial Pb isotopic composition of Orgueil calculated by a single-stage evolution model is more radiogenic than that of Canyon Diablo troilite. To reconcile the U-Pb data of Orgueil and Allende, we propose that the initial lead isotopic composition of the carbonaceous chondrites was slightly different from that of Canyon Diablo troilite Pb.