Complexation of dimethylsulfide with mercuric ion in aqueous solutions

The tendency of dimethylsulfide (DMS) to form complexes with heavy metal ions in aqueous solutions and the factors that influence it have been investigated. Among five heavy metal ions examined (Cu²⁺, Cd²⁺, Zn²⁺, Pb²⁺ and Hg²⁺), only Hg²⁺ bound significantly with DMS in aqueous solutions in which Hg²⁺ concentration was increased to much higher levels than that of natural seawater. The complexation capacity of Hg²⁺ for DMS was influenced by pH and media. The affinity of Hg²⁺ for DMS was generally lower at high than at low pH, presumably due to the competition of hydroxide ion to form hydroxomercury species. In different solutions, the affinity of Hg²⁺ for DMS followed the following sequence: ultra-purified water > 35‰ NaCl solution > seawater. It seems apparent that chloride had a negative impact on the complexation of DMS by Hg²⁺, owing to the competition of chloride with DMS for complexing Hg²⁺. In addition, the affinity of Hg²⁺ for DMS in the bulk seawater appeared to be higher than that in the surface microlayer seawater. The tendency of Hg²⁺ to form complexes with DMS in aqueous solution can be reduced by the presence of 2 mM amino-acid such as glycine, alanine, serine and cysteine, as these ligands give stable mercury complexes. However, the presence of 2 mM acetate in experimental solutions had no significant effect on the complexation of Hg²⁺ with DMS, even though this ligand has a relatively strong complexing capacity for Hg²⁺. Although mercury ions appeared to have a strong affinity for DMS, the concentration of mercury in seawater is too low to produce a great effect on the distribution of DMS in oceans.     

Behaviors of 210Pb and 210Po around hydrothermal vents in the Okinawa Trough

Vertical profiles for the uranium-series radioisotopes 210Pb and 210Po were obtained at thetwo hydrothermal vent sites, the Iheya Ridge and the Minami-Ensei Knoll, in the Mid-Okinawa Trough in 1993 and 1994, respectively. In 1995, both radioisotopes were measured at the Minami-Ensei Knoll a-gain. At the Iheya Ridge, where the hydrothermal activity is not active as reflected by the CH_4, and 222Rn data, both the total 210Pb and 210Po activities show deficiency relative to their parents, and the mean residence time of 210Pb and 210Po is approximately equal to 20 and 2-5 a, respectively. At the Minami-Ensei Knoll, which is characterized by black smokers, the total 210Pb(0.167 × 10~(-3)-2.5 × 10~(-3)_ Bq/kg) around the plumes is deficient relative to 226Ra but the total 210Po activities (1.83 × 10 ~(-3) - 2.83 × 10~(-3) Bq/kg) are in excess relative to 210Pb. The 210Po activities are higher than those in the East China Sea and the Okinawa Trough and excess 210Po has been found. The 210Pb/226Ra and 210Po/     

Dimethylsulfide in coastal zone of the East China Sea

Dimethylsulfide (DMS) in seawater were observed four times from February 1993 to August 1994 along a fixed section (PN line) in the East China Sea. The DMS concentrations showed remarkable temporal and spatial variations. The DMS concentrations were generally higher in the upper euphotic layer of the continental shelf zone in summer. The spatial variation, however, was more pronounced even in well mixed winter water, where the concentration of DMS varied widely from 3 to 106 ng-S/l in the continental shelf zone while the salinity was vertically almost uniform. This means that DMS in seawater is rapidly produced and decomposed with a time scale less than one month in the water column. The largest value of 376 ng-S/l was obtained at 5 m depth near the mouth of Changjiang River in August 1994. The mean concentrations in the surface 30 m layer in the continental shelf zone were 21, 54, 126 and 57 ng-S/l in February, October, June and August, respectively, which were about twice as large as those in the Kuroshio region. The mean fluxes of DMS from the East China Sea to the atmosphere are estimated to be 49 g-S/m²/day in winter and 194 g-S/m²/day in summer in the continental shelf zone, and to be 32 and 107 g-S/m²/day in the Kuroshio region.     

Very low frequency Ocean Bottom ambient seismic noise and coupling on the shallow continental shelf

Sources of very low frequency (0.01 to 1.0 Hz) ambient seismic noise in the shallow (<100 m) water continental margin sediments are investigated using Ocean Bottom Seismometers (OBS). The predominant seismic motions are found to be due to surface gravity (water) waves and water-sediment interface waves. Actual experimental measurements of seabed acceleration and hydrodynamic pressure are given, including side by side comparisons between buried and plate-mounted OBS units. OBS-sediment resonant effects are found to be negligible at the low frequencies under investigation. Wherever there exists relative motion between the seabed and the water, however, an exposed OBS is subject to added mass forces that cause it to move with the water rather than the sediments. Calculations based on measured seabed motions show that a neutral density, buried seismometer has superior sediment coupling charactersitics to any exposed OBS design.     

Detection of a new interstellar molecule, H2CN

We have detected a new interstellar molecule, H2CN (methylene amidogen), in the cold, dark molecular cloud TMC-l. The column density of H2CN is estimated to be approximately 1.5 x 10(11) cm-2 by assuming an excitation temperature of 5 K. This column density corresponds to a fractional abundance relative to H2 of approximately 1.5 x 10(-11). This value is more than three orders of magnitude less than the abundance of the related molecule HCN in TMC-1. We also report a tentative detection of H2CN in Sgr B2(N). The formation mechanism of H2CN is discussed. Our detection of the H2CN molecule may suggest the existence of a new series of carbon-chain molecules, CH2CnN (n = 0, 1, 2,...).     

Direct ascent to the surface of asthenospheric magma in a region of convex lithospheric flexure

The stress field of oceanic lithosphere controls the distribution of submarine petit-spot volcanoes. However, the eruption sites of these petit-spot volcanoes are considered to be limited to concavely flexed regions of lithosphere off the outer rise. Here, we present new data for a recently identified petit-spot lava field on a convexly flexed section of the lithosphere adjacent to the subduction zone offshore of northeast Japan in an area containing more than 80 volcanoes. This area is marked by strongly alkaline lavas that were erupted on the convexly flexed region. As for the concavely flexed region where the petit-spots previously reported, the base of the lithosphere beneath the eruption sites is under extension, whereas the upper part of the lithosphere is under compression. This change in the stress field, from the lower to upper lithosphere, causes ascending dikes to stall in the mid-lithosphere, leading to metasomatic interaction with the surrounding peridotite. The new geochemical data of rocks and xenocrysts presented in this study indicate that strongly alkaline magmas erupted on the convexly flexed region would have ascended more rapidly through the mid-depth of lithosphere because of the extensional regime of the upper lithosphere and decreasing the degree of metasomatic reaction with the surrounding mantle peridotite. The results indicate that the degree of metasomatism and the compositional variations of petit-spot magmas are controlled mainly by the stress field of the lithosphere.     

Distribution of glycerol dialkyl glycerol tetraethers, alkenones and polyunsaturated fatty acids in suspended particulate organic matter in the East China Sea

We investigated the spatial distribution of glycerol dialkyl glycerol tetraethers (GDGTs), alkenones, and polyunsaturated fatty acids in particulate organic matter collected at four sites along a depth transect from the continental shelf to the Okinawa Trough in the East China Sea during the spring bloom in 2008. The maximum alkenone concentration appeared in the top 25?m at all sites and the $ U_{37}^{{{\text{K}}'}} $ values were consistent with in situ water temperatures in the depth interval, suggesting that the alkenones were produced mainly in surface water. At the slope and shelf sites, GDGTs in the water column showed a concentration maximum at 74?C99?m depth, and the $ {\text{TEX}}_{86}^{\text{H}} $ agreed with in situ water temperatures, suggesting the in situ production of GDGTs in the depth interval. The low-salinity surface water above 20?m depth was characterized by low GDGT concentrations and low $ {\text{TEX}}_{86}^{\text{L}} $ -based temperatures, suggesting either the production of GDGTs in winter season or the lateral advection of GDGTs by an eastward current. At the slope and Okinawa Trough sites, TEX₈₆-based temperatures were nearly constant in the water column deeper than 300?m and corresponded to temperatures at the surface and near-surface waters rather than in situ temperatures. This observation is consistent with a hypothesis that Thaumarchaeota cells produced in surface waters are delivered to deeper water and also indicates that the residence time of suspended GDGTs in the deep-water column is large enough to mix the GDGTs produced in different seasons.     

Phytoplankton community reorganization driven by eutrophication and warming in Lake Biwa

We compiled and analyzed long-term data, including chemical, physical and phytoplankton community data, for the Lake Biwa ecosystem from 1962 to 2003. Analyses on environmental data indicate that Lake Biwa had experienced intensified eutrophication (according to total phosphorus concentration) in the late 1960s and returned to a less eutrophic status around 1985, and then exhibited rapid warming and thus increased water column stability since 1990. Total phytoplankton cell volume largely followed the trend of total phosphorus concentration, albeit short-term fluctuations existed. However, phytoplankton community shifted dramatically in response to those changes of environmental states. These shifts were cause by changes in trophic status driven by phosphorus loadings and physical properties in the water column driven by warming. Moreover, most phytoplankton species did not show a strong linear correlation with environmental variables, suggesting nonlinear transitions among different states.     

A 27-kyr record of environmental change in central Asia inferred from the sediment record of Lake Hovsgol,northwest Mongolia

Geochemistry of a sediment core from Lake Hovsgol, northwest Mongolia provides a continuous, 27-kyr history of the response of the lake and the surrounding catchment to climate change. Principle component (PC) analysis of 19 major and trace elements, total inorganic carbon (TIC), and total organic carbon (TOC) in the bulk sediment samples revealed that the 21 chemical components can be grouped into four assemblages—group-1: Na, Mg, Ca, Sr, and TIC, hosted in carbonate minerals (calcite, dolomite, and magnesian calcite); group-2: Ni, Cu, and Zn, recognized as biophilic trace metals, and TOC; group-3: Al, K, Ti, V, Fe, Rb, Cs, Ba, and Pb, composed of rock-forming minerals; and group-4: Cr, Mn, and As, sensitive to the redox condition of the sediment. The four element assemblages originated from three relevant processes. Group-1 and group-2 components are authigenic products and comprise the end member on the PC-1 score, whose variation reflects changes in the water volume, i.e. the balance between precipitation and evaporation (P/E). Group-3 components from detrital materials of the catchment contribute to the PC-2 score, whose variability indicates erosion/weathering intensity in the drainage basin, which might be controlled by the amount of vegetation cover associated with moisture change. The group-4 components of redox-sensitive elements contribute to the PC-3 score and are not an end member because of their small amount. The first two PC scores suggest a sequential record of paleo-moisture evolution in central Asia. The P/E balance in the Lake Hovsgol region, inferred from the PC-1 score, gradually increased during the glacial/interglacial transition. This resembles climate change of the North Atlantic region on the glacial–interglacial scale, but does not reflect the abrupt climate shifts such as the warm Bølling-Allerød and the cold Younger Dryas of the North Atlantic on the millennial scale. A periodic variation of ~8.7 kyr was observed in the PC-2 score profile of detrital input to Lake Hovsgol over the last glacial and Holocene. The decrease in detrital input coincided with the copious supply of moisture from the Asian monsoon regime and the North Atlantic westerly winds to the Baikal drainage basin, which includes Lake Hovsgol. Our geochemical records from Lake Hovsgol demonstrate that the climate system of interior continental Asia was strongly influenced by change on both Milankovitch and sub-Milankovitch scales.