Satellite detection of red tide in Ariake Sound, 1998–2001

High resolution SeaWiFS data was used to detect red tide events that occurred in the Ariake Sound, Japan, a small embayment known as one of the most productive areas in Japan. SeaWiFS chlorophyll data clearly showed that a large red tide event, which damaged seaweed (Nori) cultures, started early in December 2000 in Isahaya Bay, expanded to the whole sound and persisted to the end of February 2001. The monthly average of SeaWiFS data from May 1998 to December 2001 indicated that the chlorophyll peaks appeared twice a year, in early summer and in fall, after the peaks of rain and river discharge. The SeaWiFS data showed that the red tide event during 2000–2001 winter was part of the fall bloom; however, it started later and continued significantly longer than other years. Satellite ocean color data is useful to detect the red tide; however the algorithms require improvement to accurately estimate chlorophyll in highly turbid water and in red tide areas.     

Excess CO2 and pHexcess in the Intermediate Water Layer of the Northwestern Pacific

Excess CO₂ and pH_excess showing an increase in dissolved inorganic carbon and a decrease in pH from the beginning of the industrial epoch (middle of the 19th century) until the present time have been calculated in the intermediate water layer of the northwestern Pacific and the Okhotsk Sea. It is concluded that: (1) The Kuril Basin (Okhotsk Sea) and the Bussol' Strait areas are characterized by the greatest concentrations of excess CO₂ at isopycnal surfaces due to the processes of formation and transformation of intermediate water mass. (2) The largest difference in excess CO₂ concentration between the Okhotsk Sea and the western subarctic Pacific (about 8 µmol/kg) is found at the = 27.0. (3) The difference in excess CO₂ between the western subarctic Pacific and subtropical regions is significant only in the upper part of the intermediate water layer ( = 26.7–27.0). (4) About 10% of the excess CO₂ accumulation in the subtropical north Pacific is determined by water exchange with the subarctic Pacific and the Okhotsk Sea.     

Distributions and upward fluxes of particulate matter near bottom in the southeastern Bering Sea Shelf

Time-series measurements of temperature, salinity, suspended matter and beam attenuation coefficient () were measured at four hour intervals for about two days in June/ July 1982 in the middle shelf region and the coastal region of the southeastern Bering Sea. Current meters were also moored at the same locations.Depth-time distributions of indicated that profiles of suspended matter resulted from a combined process of resuspension of underlying sediments and sinking of suspended particles. Average-values for all measurements for particles revealed that the upward transport of particles due to resuspension formed a boundary layer, with a thickness apparently related to scalar speed. The average-profiles of the particle volume concentration were assumed to result from a balance between the sinking and diffusive flux of particles under a steady state, and the upward fluxes were calculated. Within the boundary layer, values of the upward fluxes of particulate organic matter linearly decreased with the logarithm of distance from the bottom. Fluxes of organic carbon at the upper edge of the boundary layer were 0.375 gC·m^–2·day^–1 in the middle shelf region (18 m above the bottom, bottom depth=78m) and 0.484gC·m^–2·day^–1 in the coastal region (25 m above the bottom, bottom depth=33m), and fluxes of nitrogen in both regions were 0.067 gN·m^–2·day^–1. The flux of organic carbon obtained in the middle shelf region (18 m above the bottom) agreed approximately with the flux (0.416 gC·m^–2·day^–1) calculated by substituting primary production data into the empirical equation of Suess (1980).     

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.     

Titanium- and water-rich metamorphic olivine in high-pressure serpentinites from the Voltri Massif (Ligurian Alps,Italy): evidence for deep subduction of high-field strength and fluid-mobile elements

Titanium- and water-rich metamorphic olivine (Fo 86–88) is reported from partially dehydrated serpentinites from the Voltri complex, Ligurian Alps. The rocks are composed of mostly antigorite and olivine in addition to magnetite, chlorite, clinopyroxene and Ti-clinohumite. In situ secondary ion mass spectrometry (SIMS) data show that metamorphic olivine has very high and strongly correlated H₂O (up to 0.7 wt%) and TiO₂ contents (up to 0.85 wt%). Ti-rich olivine shows colourless to yellow pleochroism. Olivine associated with Ti-clinohumite contains low Ti, suggesting that Ti-rich olivine is not the breakdown product of Ti-clinohumite. Fourier transform infrared spectroscopy (FTIR) absorption spectra show peaks of serpentine, Ti-clinohumite and OH-related Si vacancies. Combining FTIR and SIMS data, we suggest the presence of clustered planar defects or nanoscale exsolutions of Ti-clinohumite in olivine. These defects or exsolutions contain more H₂O (x ~ 0.1 in the formula 4Mg₂SiO₄·(1?x)Mg(OH,F)₂·xTiO₂) than Ti-clinohumite in the sample matrix (x = 0.34–0.46). In addition to TiO₂ and H₂O, secondary olivine contains significant Li (2–60 ppm), B (10–20 ppm), F (10–130 ppm) and Zr (0.9–2.1 ppm). It is enriched in ¹¹B (δ¹¹B = +17 to +23 ‰). Our data indicate that secondary olivine may play a significant role in transporting water, high-field strength and fluid-mobile elements into the deeper mantle as well as introduce significant B isotope anomalies. Release of hydrogen from H₂O-rich olivine subducted into the deep mantle may result in strongly reduced mantle domains.     

Accretionary rims on inclusions in the Allende meteorite

Many inclusions in Allende, particularly those with irregular shapes, are surrounded by a sequence of thin layers which differ from one another in texture, mineralogy and mineral-chemistry. The layer underlying all others contains either: IA, pyroxene needles + olivine + clumps of hedenbergite and andradite; IB, olivine doughnuts; or IC, rectangular olivine crystals. The next layer outward, II, contains tiny (<5 μm) olivine plates and Layer III large (5–10 μm) olivine laths. The final layer, IV, occurs as clumps of andradite + hedenbergite surrounded by magnesium-rich pyroxene needles. It separates Layer III from the Allende matrix which is more poorly sorted and more sulfide-rich than Layer III. Nepheline and iron sulfide are common constituents of most layers, the latter being particularly fine-grained and abundant in Layer II. Although not every layer is present on every inclusion, the sequence of layers is constant. Evidence that the rims are accretionary aggregates includes the presence of highly disequilibrium mineral assemblages and the fact that they are highly porous masses consisting of many euhedral crystals with few intergrowths. In addition, the layers are thickest in topographic hollows on the surfaces of inclusions and the inner layers are absent or discontinuous beyond such irregularities, suggesting that the probability of accretion of crystals was low initially, except in pockets, and became greater later, after a soft cushion of accreted condensate crystals had already formed. Separation of assemblages of different mineralogy, mineral-chemistry and texture into different rim layers seems best explained by nebular models in which long, slow cooling histories allow differentiation during condensation by grain/gas separation processes.     

软流圈熔体地幔交代作用过程中的铂族元素行为

南美洲南部的Pali Aike火山岩区第四纪碱性玄武岩中普遍发育含石榴石的斜方辉石岩包体。这种斜方辉石岩既作为独立的捕掳体存在又以细脉的形式穿插于橄榄岩捕掳体中。斜方辉石岩普遍含富Ti矿物,并且次生斜方辉石含橄榄石和单斜辉石残晶。与含石榴石橄榄岩中的斜方辉石相比,这种次生的斜方辉石以高TiO2、中等含量的Al2O3以及低Mg#为特征,表明它是在一种高度分异演化的富Ti熔体交代作用下通过消耗橄榄石和单斜辉石方式形成的。斜方辉石岩全岩的Co、Ni略低,Cr和铂族元素(PGE)含量与地幔橄榄岩相当,表明这些元素在交代作用过程中相对稳定,而交代介质带入的组分以碱质(K2O+Na2O)、Ti、Si、Al和S为主。交代的斜方辉石在现代活动岛弧和古克拉通的地幔橄榄岩捕掳体中多有报道。与这些环境中地幔样品的斜方辉石相比,PaliAike地区的次生斜方辉石含有相对高的Ti和Al,以及相对低的Mg。高Ti低Mg属性反映了交代介质可能来源于下伏的软流圈地幔并且经历了高度的分异和演化过程。Pali Aike地区所见到的这种交代斜方辉石和斜方辉石岩在其他被上涌软流圈影响的陆下岩石圈地幔中可能普遍存在。这些研究对了解中国华北-东北中生代以来的岩石圈地幔减薄机制有着重要的借鉴意义。     

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.