Upwelling plumes in sagami bay and adjacent water around the Izu Islands,Japan

Water plumes, 20 km long or less, identified by low temperature, high salinity and high nutrient concentrations, were observed on the eastern side of Izu Islands where the Kuroshio Current or its branch flowed eastward. The T-S diagrams and the vertical profiles of oceanographic variables indicated that the water plumes resulted from the upwelling of subsurface water. A newly formed plume, characterized by a sharp temperature front and high nutrient concentrations, contained less chlorophyll than did old plumes. It is suggested that the upwelling plumes are maintained for a period long enough to allow luxuriant growth of phytoplankton.     

A deep ROV "DOLPHIN 3K": Design and performance analysis

DOLPHIN 3K is a tethered remotely operated vehicle (ROV) system for ocean bottom surveys down to a depth of 3300 m. The system will be completed in fiscal year 1986. This paper describes the design of the system, and analyzes the maneuverability of the vehicle and the transmission performance of the optical fiber data communication system.     

Metal binding to dissolved organic matter and adsorption to ferrihydrite in shallow peat groundwaters: Application to diamond exploration in the James Bay Lowlands,Canada

The speciation and solubility of kimberlite pathfinder metals (Ni, Nd, Ba and K) in shallow peat groundwaters is investigated over the Yankee, Zulu and Golf kimberlites in the Attawapiskat region, James Bay Lowlands, Canada. The purpose of this study is to examine the relationship between dissolved organic matter (DOM) complexation with kimberlite pathfinder metals and determine the spatial distribution of those metals in shallow peat groundwaters along sampling transects over subcropping kimberlites. Nickel, Nd, Ba and K complexation with DOM and the adsorption of these metals onto ferrihydrite were calculated using Visual MINTEQ 3.0 and the NICA-Donnan database. Calculations predict almost 100% of soluble Nd, Ni and Ba form complexes with DOM at sampling sites with little to no contribution from upwelling groundwater (i.e., dissolved organic C (DOC) concentrations = 40–132 mg/L, pH = 3.9–5.5, and log ionic strength ??3). In only the most ombrotrophic peat groundwater conditions does a majority fraction of K bind to DOM. By contrast, under conditions with large contributions from upwelling groundwaters (i.e., DOC concentrations ?40 mg/L, pH = 5.5–6.5, and log ionic strength = ?3 to ?2), as little as 10% of Nd and Ni, and 0% K and Ba are predicted to complex with DOM. The modeling calculations suggest the dominant control on metal–DOM complexation, particularly with respect to Ni and Nd, is competitive effects for DOM binding sites due to elevated ionic strength where there is evidence of strong groundwater upwelling. Visual MINTEQ modeling of metal adsorption on ferrihydrite surfaces predicts that under strong upwelling conditions, Ni and Nd are scavenged from solution due to increased ferrihydrite precipitation and decreased fractions of metals complexed with DOM. Analytical geochemical data are consistent with model predictions of metal adsorption on ferrihydrite. Total dissolved Ni and Nd concentrations at sites of strong upwelling are up to five times lower than waters with little to no upwelling and log ferrihydrite saturation indices (logSI_ferr) indicate precipitation (values up to 5) at sites of strong groundwater upwelling. Where the majority of Ni and Nd complex with DOM and ferrihydrite is highly under saturated (logSI_ferr = ?18 to ?5), the concentrations of total Ni and Nd are elevated compared to other sites along sampling transects. Metal complexation with DOM effectively inhibits metal scavenging from solution via adsorption and/or from forming secondary mineral precipitates. Also, because alkaline earth metals do not compete strongly with Ni and Nd for adsorption sites on ferrihydrite surfaces, but do compete strongly for insoluble organic sites, Ni and Nd are more likely to adsorb onto ferrihydrite.     

The Hemlo gold deposit,Ontario: A geochemical and isotopic study

The Hemlo deposit, near Marathon, Ontario, is one of the largest gold deposits in North America. It is stratiform within Archean metamorphosed volcano-sedimentary rocks. The main ore zone is composed of pyritic, sericitic schist, and massive barite. This is the first report of stratiform barite in the Archean of North America, but other occurrences have since been found west of Hemlo. The mineralization is substantially enriched in Au, Mo, Sb, Hg, Tl and V and lacks carbonate. Because of metamorphism and deformation of the body its genesis is uncertain.${}^{87}\text{Sr}{}^{86}\text{Sr}$ of .7017 for barite from the deposit is similar to that of the sedimentary barite west of Hemlo and to initial ratios of contemporaneous volcanic rocks. At the base of the main ore zone, barite with δ^34S of +8 to +12%. was deposited with ~0%. pyrite. Upward, both barite and pyrite get isotopically lighter, with minimum values for pyrite, to ?17.5%, in non-baritic schist forming the upper part of the ore zone. In drill section, Au grades correlate with the isotopic composition of pyrite. This, and the association of fractionated sulphide with sulphate, suggests that Au, pyrite and barite were deposited contemporaneously. The linked, asymmetric distributions of S minerals and isotopic distributions, which are continuous from section to section, and the isotopic similarity of the Hemlo and western barites are consistent with a syngenetic depositional model.Two sources for the S minerals are considered. In the first, exogenous sulphate from a restricted basin were partially reduced in a geothermal system to form ³⁴S-depleted sulphide. In the second, the sulphate and sulphide are of magmatic-hydrothermal origin. Sulphate and fractionated sulphide are uncommon in Archean rocks, but one or both occur with unusual frequency in major Archean gold deposits. Hydrothermal fluids of moderately high , containing sulphate and permitting isotopic fractionation between oxidized and reduced S species, may have favoured the dissolution, transport and precipitation of Au.     

Fossil worm tubes from the presumed cold-seep carbonates of the Miocene Hayama Group, Central Miura Peninsula, Japan

Abstract Fossil worm tubes were collected from the Hayama Group, Miura Peninsula, Japan, together with abundant fossils of Calyptogena-Acharax clams. The fossil worm tubes were well preserved and coated with milky white amorphous silica. Most of the tubes were 1-3 mm in diameter, and up to 10 cm in length. Worm tubes were found in siltstone and limestone, and formed network-like assemblages. Elemental mapping on the tube cross-sections revealed the localization of sulfur, zinc and iron at the worm tubes, which suggests that sulfur-related metabolism and deposition occurred in association with the worm tubes. High resolution analysis revealed the localization of zinc-sulfur (sphalerite, ZnS) on the tubes, while iron-sulfur (pyrite, FeS₂) was localized at the center of the tubes. The spatially separate sphaleritization and pyritization imply that epiphytic and endosymbiotic microorganisms perform different sulfur metabolisms, such as sulfate-reduction and sulfide-oxidation.     

Effects of mass loss for highly-irradiated giant planets

We present calculations for the evolution and surviving mass of highly-irradiated extrasolar giant planets (EGPs) at orbital semimajor axes ranging from 0.023 to 0.057 AU using a generalized scaled theory for mass loss, together with new surface-condition grids for hot EGPs and a consistent treatment of tidal truncation. Theoretical estimates for the rate of energy-limited hydrogen escape from giant-planet atmospheres differ by two orders of magnitude, when one holds planetary mass, composition, and irradiation constant. Baraffe et al. [Baraffe, I., Selsis, F., Chabrier, G., Barman, T.S., Allard, F., Hauschildt, P.H., Lammer, H., 2004. Astron. Astrophys. 419, L13-L16] predict the highest rate, based on the theory of Lammer et al. [Lammer, H., Selsis, F., Ribas, I., Guinan, E.F., Bauer, S.J., Weiss, W.W., 2003. Astrophys. J. 598, L121-L124]. Scaling the theory of Watson et al. [Watson, A.J., Donahue, T.M., Walker, J.C.G., 1981. Icarus 48, 150-166] to parameters for a highly-irradiated exoplanet, we find an escape rate ∼¹⁰² lower than Baraffe's. With the scaled Watson theory we find modest mass loss, occurring early in the history of a hot EGP. In this theory, mass loss including the effect of Roche-lobe overflow becomes significant primarily for masses below a Saturn mass, for semimajor axes ?0.023 AU. This contrasts with the Baraffe model, where hot EGPs are claimed to be remnants of much more massive bodies, originally several times Jupiter and still losing substantial mass fractions at present.     

Probabilistic aspects of micropaleontologic assemblage zones

A micropaleontologic assemblage zone is defined by occurrence of some characteristic species among many coeval species. When number of assemblage-defining species and total number of species observed are designated as Aand N,respectively, the ratio, A/N,is strongly dependent on duration of the assemblage. Theoretical consideration on the basis of a micropaleontologic cohort model shows that, when origination rate and extinction rate of species are obtained, the most reasonable ratio (A/N) and duration of the assemblage can be determined. The probabilistic model described in this paper provides a theoretical relation between the ratio and the duration. Inaccuracy in correlating micropaleontologic data to certain assemblage zones established can not be avoided because of many natural sorting and artificial biases. Ambiguity arising when data with a small number of characteristic species are correlated with a certain assemblage is numerically estimated.     

Oxidized sulfur-rich mafic magma at Mount Pinatubo,Philippines

Basaltic fragments enclosed in andesitic dome lavas and pyroclastic flows erupted during the early stages of the 1991 eruption of Mount Pinatubo, Philippines, contain amphiboles that crystallized during the injection of mafic magma into a dacitic magma body. The amphiboles contain abundant melt inclusions, which recorded the mixing of andesitic melt in the mafic magma and rhyolitic melt in the dacitic magma. The least evolved melt inclusions have high sulfur contents (up to 1,700 ppm) mostly as SO₄ ^2–, which suggests an oxidized state of the magma (NNO+1.4). The intrinsically oxidized nature of the mafic magma is confirmed by spinel–olivine oxygen barometry. The value is comparable to that of the dacitic magma (NNO+1.6). Hence, models invoking mixing as a means of releasing sulfur from the melt are not applicable to Pinatubo. Instead, the oxidized state of the dacitic magma likely reflects that of parental mafic magma and the source region in the sub-arc mantle. Our results fit a model in which long-lived SO₂ discharge from underplated mafic magma accumulated in the overlying dacitic magma and immiscible aqueous fluids. The fluids were the most likely source of sulfur that was released into the atmosphere during the cataclysmic eruption. The concurrence of highly oxidized basaltic magma and disproportionate sulfur output during the 1991 Mt. Pinatubo eruption suggests that oxidized mafic melt is an efficient medium for transferring sulfur from the mantle to shallow crustal levels and the atmosphere. As it can carry large amounts of sulfur, effectively scavenge sulfides from the source mantle and discharge SO₂ during ascent, oxidized mafic magma forms arc volcanoes with high sulfur fluxes, and potentially contributes to the formation of metallic sulfide deposits.Editorial responsibility: J. Hoefs

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The structure of monomeric and dimeric uranyl adsorption complexes on gibbsite: A combined DFT and EXAFS study

We investigated the structure of uranyl sorption complexes on gibbsite (pH 5.6-9.7) by two independent methods, density functional theory (DFT) calculations and extended X-ray absorption fine structure (EXAFS) spectroscopy at the U-L_III edge. To model the gibbsite surface with DFT, we tested two Al (hydr)oxide clusters, a dimer and a hexamer. Based on polarization, structure, and relaxation energies during geometry optimization, the hexamer cluster was found to be the more appropriate model. An additional advantage of the hexamer model is that it represents both edges and basal faces of gibbsite. The DFT calculations of (monomeric) uranyl sorption complexes show an energetic preference for the corner-sharing versus the edge-sharing configuration on gibbsite edges. The energy difference is so small, however, that possibly both surface species may coexist. In contrast to the edge sites, sorption to basal sites was energetically not favorable. EXAFS spectroscopy revealed in all investigated samples the same interatomic distances of the uranyl coordination environment (R_U-Oax ≈ 1.80 Å, R_U-Oeq ≈ 2.40 Å), and towards the gibbsite surface (R_U-O ≈ 2.87 Å, R_U-Al ≈ 3.38 Å). In addition, two U-U distances were observed, 3.92 Å at pH 9.7 and 4.30 Å at pH 5.6, both with coordination numbers of ∼1. The short U-U distance is close to that of the aqueous uranyl hydroxo dimer, UO₂(OH)₂, reported as 3.875 Å in the literature, but significantly longer than that of aqueous trimers (3.81-3.82 Å), suggesting sorption of uranyl dimers at alkaline pH. The longer U-U distance (4.30 Å) at acidic pH, however, is not in line with known aqueous uranyl polymer complexes. Based on the EXAFS findings we further refined dimeric surface complexes with DFT. We propose two structural models: in the acidic region, the observed long U-U distance can be explained with a distortion of the uranyl dimer to form both a corner-sharing and an edge-sharing linkage to neighboring Al octahedra, leading to R_U-U = 4.150 Å. In the alkaline region, a corner-sharing uranyl dimer complex is the most favorable. The U-O path at ∼2.87 Å in the EXAFS spectra arises from the oxygen atom linking two Al cations in corner-sharing arrangement. The adsorption structures obtained by DFT calculations are in good agreement with the structural parameters from EXAFS analysis: U-Al (3.394 Å), U-U (3.949 Å), and U-O (2.823 Å) for the alkaline pH model, and U-Al (3.279 Å), U-U (4.150 Å), and U-O (2.743 Å) for the acidic pH model. This work shows that by combining EXAFS and DFT, consistent structural models for uranyl sorption complexes can be obtained, which are relevant to predict the migration behavior of uranium at nuclear facilities.