Distributions of aluminum, manganese, cobalt, and lead in the western South Pacific: Interplay between the South and North Pacific

Aluminum (Al), manganese (Mn), cobalt (Co), and lead (Pb) are strongly scavenged from seawater. We reported that each element is uniquely related to ocean circulation in the North Pacific (Zheng et al., 2019). Herein, we present the full-depth distributions of these elements in the western South Pacific, which include meridional sections along 170°W (GEOTRACES GP19). We determined dissolved (d) and total dissolvable (td) concentrations using filtered and unfiltered seawater without UV treatment, and we calculated labile particulate (lp) concentrations as the difference between td and d concentrations. This and the previous studies present the basin scale distributions, which enable us to investigate first order processes that drive the biogeochemistry of Al, Mn, Co, and Pb in the Pacific Ocean. The meridional section of dAl along 170°W (GP19)-160°W (GPc06) from 64°S to 54°N indicates that elevated concentrations (maximum 6.1 nmol/kg) occur between 40°S and 10°S from surface to bottom. However, the maxima of lpAl occur at high latitudes. The lpAl/tdAl ratio has a minimum of 0.26 ± 0.12 (ave ± sd, n = 116) in the zone from 30°S to 0°S. Based on these results, we propose a hypothesis that weathering on land has a significant effect on the distribution of Al in the ocean. Intensive weathering on tropical and subtropical islands and Australia forms kaolinite-dominated soils and laterite. This process provides dAl and kaolinite to the ocean. The supply of kaolinite results in kaolinite-dominated sediments that become a major bottom source for dAl. In contrast, strong sources of Mn and Co are continental shelves around the northern boundary. Dissolved Mn and dCo are released from sediments by manganese reduction and carried by intermediate water circulation. In particular, dCo spreads in the North Pacific Intermediate Water (NPIW), Equatorial Pacific Intermediate Water (EqPIW), and Antarctic Intermediate Water (AAIW); 23–59 pmol/kg at a potential density anomaly (σθ) of 27.0. This is partly owing to the uptake of dCo by phytoplankton and remineralization from settling particles. The dPb concentrations are 10 ± 6 pmol/kg (n = 397) in the South Pacific and 30 ± 20 pmol/kg (n = 566) in the North Pacific. The distribution of dPb is characterized by a maximum in the Subtropical Mode Water (SMW) and Central Mode Water (CMW) with σθ∼26 in the North Pacific. These results indicate that Pb is predominantly supplied by anthropogenic aerosols from Asia and Russia to the Pacific Ocean. Because Pb is not actively taken up by phytoplankton, Pb enters mode waters during winter convection and is transported with mode waters

希土類元素水酸化物による水中微量金属の共沈濃縮-定量に関する研究

取得学位：博士(工学)，学位授与番号：博乙第300号，学位授与年月日：平成18年3月22日,学位授与年：200

Sectional Distribution Patterns of Cd, Ni, Zn, and Cu in the North Pacific Ocean: Relationships to Nutrients and Importance of Scavenging

The North Pacific Ocean is located at the end of the thermohaline circulation of deep water. This study reports on basin-scale full-depth sectional distributions of total dissolvable (td), dissolved (d), and labile particulate (lp) Cd, Ni, Zn, and Cu along three transects: the GEOTRACES transects GP18 (165°E) and GP02 (47°N), and along 160°W. We find that scavenging is an important factor that significantly affects the distributions of dZn, dNi, and dCu, of which the magnitude of influence increases in the order of Cd 800 m deep, which is in the range of the phytoplankton Cd/P ratio. This is indicative of the dominant effect of water circulation and biological processes on dCd distribution. The dissolved metals (dMs) to PO₄ ratios of other examined metals were either partially or completely outside the range of typical biomass ratios. They generally increased with depth in waters >800 m deep; the magnitude of increase was the highest for Cu and moderate for Ni and Zn. Below 800 m, an increase in the apparent oxygen utilization from 150 to 300 μmol/kg was concurrent with a decrease in the dMs/PO4 ratios: 4 ± 3% for Cd, 21 ± 4% for Zn, 21 ± 3% for Ni, and 69 ± 7% for Cu

Determination of cobalt and nickel by graphite-furnace atomic absorption spectrometry after coprecipitation with scandium hydroxide

金沢大学教育学部理科教

Determination of chromium, copper and lead in river water by graphite-furnace atomic absorption spectrometry after coprecipitation with terbium hydroxide

金沢大学教育学部理科教

Selective coprecipitation of chromium(Ⅲ)in water with scandium hydroxide prior to graphite furnace atomic absorption spectrometric determination

金沢大学教育学部理科教

Determination of cadmium in spring water by graphite-furnace atomic absorption spectrometry after coprecipitation with ytterbium hydroxide

金沢大学教育学部理科教

Distribution and stoichiometry of Al, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb in the East China Sea

The dissolved (d) and total dissolvable (td) trace metals were determined in seawater samples collected from the East China Sea (ECS). Labile particulate (lp) species was calculated as td minus d, and the sectional and vertical distributions of d and lp trace metals were evaluated. The surface concentrations of dAl, dCo, dNi, dCu, and dPb were higher in the continental shelf region than in the Kuroshio region. lpAl and lpFe were the dominant species below a depth of 400 m, and a strong positive correlation was observed between them in the Kuroshio region. The enrichment factor (EF) against crustal abundance was calculated for the purpose of estimating the origin of dMs in the ECS. The EF(dFe) was close to unity. These results suggest that both lpFe and dFe are dominated by crustal sources. The other elements had high EF, indicating significant contributions from other sources. EF(dPb) was close to the enrichment factor in aerosol, suggesting atmospheric input from anthropogenic sources. The dM/P ratios were calculated to investigate the validity of the extended Redfield ratio in the ECS. The Mn/P, Co/P, Cu/P, Zn/P, and Cd/P ratios in shallow water (< 200 m) were within the same order of magnitude as those in phytoplankton. In contrast, the Al/P and Fe/P ratios were, respectively, 27 and 213 times higher in phytoplankton compared to those in shallow water. These results suggest that dFe is a potential limiting factor for biological production, although it is not exhausted in surface water

Stable Isotope Tracking of Endangered Sea Turtles: Validation with Satellite Telemetry and δ15N Analysis of Amino Acids

Effective conservation strategies for highly migratory species must incorporate information about long-distance movements and locations of high-use foraging areas. However, the inherent challenges of directly monitoring these factors call for creative research approaches and innovative application of existing tools. Highly migratory marine species, such as marine turtles, regularly travel hundreds or thousands of kilometers between breeding and feeding areas, but identification of migratory routes and habitat use patterns remains elusive. Here we use satellite telemetry in combination with compound-specific isotope analysis of amino acids to confirm that insights from bulk tissue stable isotope analysis can reveal divergent migratory strategies and within-population segregation of foraging groups of critically endangered leatherback sea turtles (Dermochelys coriacea) across the Pacific Ocean. Among the 78 turtles studied, we found a distinct dichotomy in δ15N values of bulk skin, with distinct “low δ15N” and “high δ15N” groups. δ15N analysis of amino acids confirmed that this disparity resulted from isotopic differences at the base of the food chain and not from differences in trophic position between the two groups. Satellite tracking of 13 individuals indicated that their bulk skin δ15N value was linked to the particular foraging region of each turtle. These findings confirm that prevailing marine isoscapes of foraging areas can be reflected in the isotopic compositions of marine turtle body tissues sampled at nesting beaches. We use a Bayesian mixture model to show that between 82 and 100% of the 78 skin-sampled turtles could be assigned with confidence to either the eastern Pacific or western Pacific, with 33 to 66% of all turtles foraging in the eastern Pacific. Our forensic approach validates the use of stable isotopes to depict leatherback turtle movements over broad spatial ranges and is timely for establishing wise conservation efforts in light of this species’ imminent risk of extinction in the Pacific

Strong elemental fractionation of Zr–Hf and Nb–Ta across the Pacific Ocean

Understanding the circulation of water masses in the world’s oceans is critical to our knowledge of the Earth’s climate system. Trace elements and their isotopes have been explored as tracers for the movement of water masses1. One type of candidate elements2 are the high-field-strength elements zirconium (Zr), hafnium (Hf), niobium (Nb) and tantalum (Ta). Here we measure the distributions of dissolved Zr, Hf, Nb and Ta along two meridional sections in the Pacific Ocean that extend from 65 to 10 S and from 10 to 50 N. We find that all four elements tend to be depleted in surface water. In the deep oceans, their concentrations rise along our transects from the Southern Ocean to the North Pacific Ocean, and show strong correlations with the concentration of silicate. These results indicate that terrigenous sources are important to the budget of Zr, Hf, Nb and Ta in sea water, compared with hydrothermal input. Unexpectedly, the weight ratios for Zr/Hf fall between 45 and 350 and those for Nb/Ta between 14 and 85 in Pacific sea water, higher than the ratios observed in fresh water, in the silicate Earth or in chondritic meteorites. We conclude that the fractionation of Zr/Hf and Nb/Ta ratios will be useful for tracing water masses in the ocean