Zircon U-Pb and Hf-O analysis of porphyries from the Duolong porphyry Cu-Au deposit in the Bangongco copper belt, central Tibet

The Duolong porphyry Cu-Au deposit (5.4 Mt at 0.72% Cu, 41 t at 0.23 g/t Au), which is related to the granodiorite porphyry and the quartz-diorite porphyry from the Bangongco copper belt in central Tibet, formed in a continental arc setting. Here, we present the zircon U-Pb ages, geochemical whole-rock, Sr-Nd whole-rock and zircon in-situ Hf-O isotopic data for the Duolong porphyries. Secondary ion mass spectrometry (SIMS) zircon U-Pb analyses for six samples yielded consistent ages of ~118 Ma, indicating a Cretaceous formation age. The Duolong porphyries (SiO2 of 58.81-68.81 wt.%, K2O of 2.90-5.17 wt.%) belong to the high-K calc-alkaline series. They show light rare earth element (LREE)-enriched distribution patterns with (La/Yb)N = 6.1-11.7, enrichment in large ion lithophile elements (e.g., Cs, Rb, and Ba) and depletion of high field strength elements (e.g., Nb), with negative Ti anomalies. All zircons from the Duolong porphyries share relatively similar Hf-O isotopic compositions (d18O=5.88-7.27 per mil; eHf(t)=3.6-7.3), indicating that they crystallized from a series of cogenetic melts with various degrees of fractional crystallization. This, along with the general absence of older inherited zircons, rules out significant crustal contamination during zircon growth. The zircons are mostly enriched in d18O relative to mantle values, indicating the involvement of an 18O-enriched crustal source in the generation of the Duolong porphyries. Together with the presence of syn-mineralization basaltic andesite, the mixing between silicic melts derived from the lower crust and evolved H2O-rich mafic melts derived from the metsomatizied mantle wedge, followed by subsequent fractional crystallization (FC) and minor crustal contamination in the shallow crust, could well explain the petrogenesis of the Duolong porphyries. Significantly, the hybrid melts possibly inherited the arc magma characteristics of abundant F, Cl, Cu, and Au elements and high oxidation state, which contributed to the formation of the Duolong porphyry Cu-Au deposit.

Composition of bottom sediments from Core SO201-2-101, Shirshov Ridge, Bering Sea

Analysis of lithology, grain-size composition, clay minerals, and geochemistry of Upper Pleistocene bottom sediments from the submarine Shirshov Ridge (Bering Sea) showed that the Yukon-Tanana terrane of the Central Alaska was main source area of the sediments. Sedimentary material was transported by the Yukon River through Beringia up to the shelf break, where they were entrained by a strong north-west sea current. Lithological data revealed several pulses of ice-rafted debris deposition roughly synchronous with Heinrich events and periods of weaker bottom current intensity. Based on geochemical results we distinguished intervals of an increase in paleoproductivity and extension of the oxygen minimum zone. Our results suggest that there were three stages of deposition driven by glacioeustatic sea-level fluctuations and glacial cycles in Alaska.

Analysis of Manganese nodules from Sonne cruises SO06/1 and /2, "Hawaii-Tahiti-Transect", Teilprojekt ICIME

Manganese nodules research has focused on the area between the Clarion Fracture Zone to the North and the Clipperton Fracture Zone to the South where significant concentrations were found ni Ni-Cu. During the CCOP/SOPAC-IOC/IDOE International workshop on the "Geology Mineral Resources and Geophysics of the South Pacific" held in Fiji in September 1975, a working group on manganese nodules was formed by scientists from: CNEXO, Brest, the Institute of Oceanography, New Zealand, Imperial College, London and the Technical University of Aachen. A draft project was presented in July 1976 by J. Andrews, University of Hawaii and G. Pautot, Cnexo on a joint survey under the name of: "Hawaii-Tahiti Transect program". Further details were worked on in September 1976 during the International Geological Congress in Sydney with the participation of D. Cronan, Imperial College, Glasby, New Zealand Geological Survey and G. Friedrich, Aachen TU. The scientific final program was established in July 1977, planning on the participation of three research vessels: the Suroit (CNEXO), the Kana Keoki (U. of Hawaii) and the Sonne (Aachen TU). Several survey areas were selected across the Pacific Ocean (Areas A, B, C, D, E, F, G and H) with about the same crustal age (about 40 million years) and a similar water depths. Being near large fault zones, the ares would be adequate to study the influences of biological productivity, sedimentation rate and possibly volcanic activity on the formation and growth of manganese nodules. The influnece of volcanic activity study would particularly apply to area G being situated near the Marquesas Fracture Zone. The cruise from R/V Sonne started in August 1978 over areas C, D, F, G K. The R/V suroit conducted a similar expedition in 1979 over areas A, B, C, D, E, H and I. Others cruises were planned during the 1979-1980 for the R/V Kana Keoki. The present text relates the R/V Sonne Cruises SO-06/1 and SO-06/2 held within the frame work of this international cooperative project.

(Table 2) Chemical composition of surface sediments from stations of Cruise 11A of R/V Akademik Mstislav Keldysh

Distributions of Mn, Fe, Cu, Cd, Cr, Co and Ni in sea water are investigated (42 samples, dissolved and particulate forms) in the vicinity of the underwater gas vent field on the northwestern slope of the Paramushir Island. While regular background distributions of the elements occur in the shore zone, there is a column of elevated concentrations of particulate matter, particulate Mn, and dissolved Mn, Fe, Cu, Cd, Cr, Co and Ni that coincides with location of the gas plume. This column can be traced as high as 780 m above the bottom. High metal concentrations in water of the plume are attributable to physico-chemical concentration at the phase interface; the source of elevated mineral concentrations is obviously flux of dissolved minerals from interstitial waters, which extends to considerable distances in vertical direction.

(Table 2) Contents of trace elements in plankton from the White Sea

With a view to more complete understanding of the role of phyto- and zooplankton in biogeochemical cycles, spatial distributions of Fe, Mn, Co, Ni, Cr, Cu, Cd, Pb, Zn, As, Hg, and Corg in the White Sea seston (21 samples) collected in August 2004 during Cruise 64 of R/V ''Professor Shtokman'' were studied. It was shown that the elements in study are accumulated in plankton with enrichment factors from 10**2 for Hg to 10**5 for Fe, as compared to seawater. Spatial distribution of trace elements is determined by sources of their supply and correlates with distribution of primary production and biomass of zooplankton. Increased values of trace element contents (excluding As) are characteristic of the Dvina Bay, whereas the highest As concentrations were found in the Kandalaksha Bay.

Concentrations of Fe, Mn, Cu, Zn, Co, Ni, Pb, Cd, B, and SiO2 in interstitial waters from bottom sediments of the Atlantis II and Discovery Deeps, Red Sea rift zone

Chemical analyzes show that interstitial waters from ore-bearing bottom sediments of the Atlantis II and Discovery Deeps are enriched in Fe, Mn, Cu, Ni, Co, Zn, Pb, and Cd compared to sea water. Enrichment factors of these trace elements in the interstitial waters of the Atlantis II Deep relative to the sea water vary within the following ranges: for Fe from 100 to 7000, for Mn from 19047 to 32738, for Zn from 500 to 1600, for Pb from 78333 to 190000, for Cu from 107 to 654. Comparison of average weighted concentrations of Fe, Mn, Zn, Pb, Cu, Ni in the bottom sediments and the interstitial waters of the Atlantis II Deep indicates common regularities and good relationship in distribution of these elements along sediment cores. Differences in concentrations and distribution of the studied trace elements in the interstitial waters of the Atlantis II and Discovery Deeps result from different chemical compositions of hydrothermal fluids entering these deeps.

Composition of native Cu, Cu isotope and mineral analysis from different samples of ODP and DSDP

Ocean drilling has revealed that, although a minor mineral phase, native Cu ubiquitously occurs in the oceanic crust. Cu isotope systematics for native Cu from a set of occurrences from volcanic basement and sediment cover of the oceanic crust drilled at several sites in the Pacific, Atlantic and Indian oceans constrains the sources of Cu and processes that produced Cu**0. We propose that both hydrothermally-released Cu and seawater were the sources of Cu at these sites. Phase stability diagrams suggest that Cu**0 precipitation is favored only under strictly anoxic, but not sulfidic conditions at circum-neutral pH even at low temperature. In the basaltic basement, dissolution of primary igneous and potentially hydrothermal Cu-sulfides leads to Cu**0 precipitation along veins. The restricted Cu-isotope variations (delta 65Cu = 0.02-0.19 per mil) similar to host volcanic rocks suggest that Cu**0 precipitation occurred under conditions where Cu+-species were dominant, precluding Cu redox fractionation. In contrast, the Cu-isotope variations observed in the Cu**0 from sedimentary layers yield larger Cu-isotope fractionation (delta 65Cu = 0.41-0.95 per mil) suggesting that Cu**0 precipitation involved redox processes during the diagenesis, with potentially seawater as the primary Cu source. We interpret that native Cu precipitation in the basaltic basement is a result of low temperature (20°-65 °C) hydrothermal processes under anoxic, but not H2S-rich conditions. Consistent with positive delta 65Cu signatures, the sediment cover receives major Cu contribution from hydrogenous (i.e., seawater) sources, although hydrothermal contribution from plume fallout cannot be entirely discarded. In this case, disseminated hydrogenous and/or hydrothermal Cu might be diagenetically remobilized and reprecipitated as Cu**0 in reducing microenvironment.

Description and chemical composition of manganese nodules collected during Hakuho Maru Cruise KH-72-2, Oct-Dec, 1972 in the Southwest Japan Arc and Ryukyu Arc areas

The cores and dredges described in this report were taken on the KH-72-2 Expedition in October-December, 1972 by the Ocean Research Institute, University of Tokyo from the R/V Hakuho Maru. A total of 21 cores and dredge sites have been recovered.