The osmium isotopic composition of convecting upper mantle deduced from ophiolite chromites

Chromites separated from the upper mantle or lower crustal portions of 18 ophiolites ranging in age from 900 Ma to 50 Ma are examined for Re-Os isotopic systematics. The ophiolites include both MORB and back arc types, although most are from supra-subduction zone (SSZ) settings. The chromites are robust indicators of the initial Os isotopic compositions of the systems sampled. There is very limited range in calculated initial γ_Os values, with the entire group averaging +1.31. Least squares linear regression of the age of chromite formation (in Ga) versus initial ¹⁸⁷Os/¹⁸⁸Os of a filtered suite yields a slope of −0.0058±0.0019 (2σ) and a present day intercept of 0.12809±0.00085 (2σ), equivalent to a γ_Os value of +0.9±0.6. Of the suite of 51 samples analyzed, 68% lie within ±1% of this evolution trajectory.Although most of the samples formed in SSZ environments, there is little evidence to suggest modification of the mantle Os isotopic composition via radiogenic melts or fluids derived from subducting slabs. The ophiolite data are interpreted as representative of the convecting upper mantle and suggest that the present isotopic composition of the convecting upper mantle averages approximately 1.2% less radiogenic than the estimated minimum composition of the primitive upper mantle of 0.1296±8 (Meisel et al., 2001). The most likely explanation for the difference is the formation, subduction and isolation of some portion of the mafic oceanic crust. Using models based on the assumption that the convecting upper mantle comprises 50% of the total mass of the mantle, and that the average isolation period for subducted oceanic crust is 1.5 to 2.0 Ga, it is estimated that approximately 2 to 3% of the total mass of the mantle is composed of subducted mafic oceanic crust that remains isolated from the convecting upper mantle. Because the isotopic compositions of the DMM and PUM overlap within uncertainties, however, the results do not require any isolated slab component.     

Chemical characterization of fractionated humic acids from lake and marine sediments

Humic acids from Recent lacustrine and marine sediments were divided into five components by extractions with organic solvents and characterized by elementary composition, ultraviolet, visible and infrared absorption spectra and n.m.r. spectra. The results suggest that sedimentary humic acids have a cyclic structure (40–50% of the total carbon), which is considered to be alicyclic rather than aromatic. No marked differences except for an absorption near 410 mμ were observed between humic acids from lake and marine sediments.     

Jurassic plume-origin ophiolites in Japan: accreted fragments of oceanic plateaus

The Mikabu and Sorachi–Yezo belts comprise Jurassic ophiolitic complexes in Japan, where abundant basaltic to picritic rocks occur as lavas and hyaloclastite blocks. In the studied northern Hamamatsu and Dodaira areas of the Mikabu belt, these rocks are divided into two geochemical types, namely depleted (D-) and enriched (E-) types. In addition, highly enriched (HE-) type has been reported from other areas in literature. The D-type picrites contain highly magnesian relic olivine phenocrysts up to Fo_93.5, and their Fo–NiO trend indicates fractional crystallization from a high-MgO primary magma. The MgO content is calculated as high as 25 wt%, indicating mantle melting at unusually high potential temperature (T _p) up to 1,650 °C. The E-type rocks represent the enrichment in Fe and LREE and the depletion in Mg, Al and HREE relative to the D-type rocks. These chemical characteristics are in good accordance with those of melts from garnet pyroxenite melting. Volcanics in the Sorachi–Yezo belts can be divided into the same types as the Mikabu belt, and the D-type picrites with magnesian olivines also show lines of evidence for production from high T _p mantle. Evidence for the high T _p mantle and geochemical similarities with high-Mg picrites and komatiites from oceanic and continental large igneous provinces (LIPs) indicate that the Mikabu and Sorachi–Yezo belts are accreted oceanic LIPs that were formed from hot large mantle plumes in the Late Jurassic Pacific Ocean. The E- and D-type rocks were formed as magmas generated by garnet pyroxenite melting at an early stage of LIP magmatism and by depleted peridotite melting at the later stage, respectively. The Mikabu belt characteristically bears abundant ultramafic cumulates, which could have been formed by crystal accumulation from a primary magma generated from Fe-rich peridotite mantle source, and the HE-type magma were produced by low degrees partial melting of garnet pyroxenite source. They should have been formed later and in lower temperatures than the E- and D-type rocks. The Mikabu and Sorachi Plateaus were formed in a low-latitude region of the Late Jurassic Pacific Ocean possibly near a subduction zone, partially experienced high P/T metamorphism during subduction, and then uplifted in association with (or without, in case of Mikabu) the supra-subduction zone ophiolite. The Mikabu and Sorachi Plateaus may be the Late Jurassic oceanic LIPs that could have been formed in brotherhood with the Shatsky Rise.     

A 35 kyr record of organic matter composition and δ13C of n-alkanes in bog sediments close to Lake Baikal: Implications for paleoenvironmental studies

We characterized the compositions of organic compounds in a Cheremushka bog sediment core (deposited over the last 35 kyr), located at the eastern coast of Lake Baikal, to obtain basic information about the terrestrial organic matter (OM) which contributed to Lake Baikal sediments. The bog sediment was analyzed for the molecular composition of n-alkanes, lignin phenols and n-C₂₄ to C₃₀ alkanoic acids, as well as the carbon isotopic composition of plant wax derived n-C₂₇ to C₃₃ alkanes.Concentrations of lignin phenols [vanillyl (V) plus syringyl (S) phenols] normalized to total organic carbon (TOC) in the Holocene are twice those for the last glacial maximum (LGM), while concentrations of TOC-normalized n-C₂₄ to C₃₀ alkanoic acids do not change markedly in this period. Thus, the ratio of lignin phenols to n-C₂₄ to C₃₀ alkanoic acids increases from the LGM to the Holocene. This result is essentially consistent with pollen analysis indicating an expansion of woody plants in the Holocene and a prevailing herb-abundant environment for the LGM. The δ¹³C values of n-C₂₇ to C₃₃ alkanes (e.g. ?29‰ to ?33‰ for C₃₁) indicate the presence of C₃-dominant plants throughout the core.The contribution of terrestrial OM to Lake Baikal sediments was estimated using the biomarkers, on the assumption that the OM in the bog sediments is a representative of the terrestrial OM around the lake. Hence, the estimation using lignin phenol or n-C₂₄ to C₃₀ alkanoic acid parameters indicates that 11–24% of the TOC in the Academician Ridge sediments is land-derived for both the Holocene and the LGM, which is similar to the estimates from C/N values of bulk OM. However, the estimates for terrestrial OM using the n-C₂₇ to C₃₃ alkane parameter are generally higher than those using lignin phenol or n-C₂₄ to C₃₀ alkanoic acid parameters. The difference is thought to be associated with the difference in source and behavior of these biomarkers.     

Decompression P–T path of coesite eclogite to granulite from Weihai, eastern China

Granulitized coesite-bearing eclogite from Weihai, northeastern part of the Shandong peninsula, eastern China was studied in detail to reveal the modification of mineral chemistry during decompression metamorphism. Considerable modification of chemical composition is recorded in clinopyroxene that occurs both as inclusions in garnet and as a matrix mineral. Careful examination of chemical variation with the change in microstructure made it possible to estimate the equilibrium composition of minerals at the coesite eclogite and garnet granulite stages. We were able to define three reference points on the P–T path, namely, coesite eclogite (3 GPa, 660±40°C), granulite (1 GPa, 700±30°C) and amphibolite (0.9 GPa, 600±20°C). The path thus obtained is similar to those obtained by previous workers and supports nearly isothermal decompression of coesite eclogite.     

Petrogenesis of greenstones from the Mino–Tamba belt, SW Japan: Evidence for an accreted Permian oceanic plateau

Permian greenstones in the Jurassic Mino–Tamba accretionary complex, southwest Japan, are divided into three distinct series on the basis of their geological occurrence, mineralogy, and geochemistry. A low-Ti series (LTS) is associated with Lower Permian chert and limestone, and is the most voluminous of the three series. The LTS shows slightly more enriched geochemical and isotopic characteristics than MORB. A transition series (TS) is mainly associated with Lower Permian chert, and has more enriched geochemical signatures than MORB. Its isotopic characteristics are divided into enriched and depleted types. A high-Ti series (HTS) occurs as sills and hyaloclastites within Middle Permian chert and as dikes intruding the TS. Some HTS rocks have high MgO contents. The HTS is characterized by enrichment in incompatible trace elements and an isotopic composition comparable to HIMU-type basalt. The geochemistry of the voluminous LTS is similar to that of the oceanic basalt series of the Kerguelen plateau, suggesting production by partial melting of a shallow mantle plume head below thick oceanic lithosphere in Early Permian time. We infer that the TS formed simultaneously at the margins of the mantle plume head. In contrast, the HTS may have resulted from partial melting of a deep mantle plume tail in Middle Permian time. Permian greenstones in the Mino–Tamba belt may have thus formed by superplume activity in an intra-oceanic setting. Given the presence of two known contemporary continental flood basalt provinces (Siberia and Emeishan) and some accreted oceanic plateau basalts, the vast magmatism of the Mino–Tamba oceanic plateau suggests a large-scale superplume pulse in Permian time. Accretion of oceanic plateaux may have played an important role in the growth of continental margins and island arcs in Japan and elsewhere in the circum-Pacific region.     

Organic geochemistry of the Japan Sea sediments-1: Bulk organic matter and hydrocarbon analyses of Core KH-79-3, C-3 from the Oki Ridge for paleoenvironment assessments

Organic geochemical study of bulk organic matter (OM), hopanoid hydrocarbon and normal hydrocarbon (C₂₃C₃₅) was conducted for a 936-cm-long sediment core sample from the Oki Ridge of the Japan Sea (Core KH-79-3, C-3; 37°03.5 N, 134°42.6E, water depth 935 m). Stable carbon isotopic ratios were also measured for both bulk OM and individual hydrocarbons. The following results were obtained: (1) The weight ratios of total organic carbon to total nitrogen range from 6.2 to 9.4 in the core. The ¹³C values of bulk OM range from –25.1–20.7%.. The ¹³C values of OM in the sections of 140190 cm are lower (–25–24) than those in the other sections (–23–21). This result indicates that OM in the core except for the 140190 cm sections is essentially of marine origin. (2) The ¹³C value of diploptene (a hopanoid hydrocarbon) in the last glacial maximum (LGM), is –66.3 (vs. PDB), which indicates it originating in methanotrophic bacteria. This result provides evidence to support for the previous ideas (Oba et al., 1980, 1984; Masuzawa and Kitano, 1984) that the bottom waters in the Japan Sea were anoxic in LGM. (3) Long chain (C₂₃C₃₅) n-alkanes of higher-plant wax origin were found throughout the core. Their concentration is high in 140190 cm in depth, suggesting that eolian dust load was high in LGM. (4) The n-alkane/TOC ratio increases with decreasing ¹³C values of bulk OM. This result indicates that the load of terrestrial (probably eolian dust-derived) OM to the Japan Sea became higher in colder climates. (5) The CPI values of long-chain n-alkanes are different in different ¹³O stages of paleoclimate, probably reflecting variations in species of terrestrial higher plants as a result of climatological adaptations.