Dissolved and labile particulate Zr,Hf, Nb,Ta, Mo and W in the western North Pacific Ocean

Dissolved and labile particulate Zr, Hf, Nb, Ta, Mo and W were determined at stations K1 (51°N, 165°E), K2 (47°N, 160°E), KNOT (44°N, 155°E) and 35N (35°N, 160°E) in the western North Pacific Ocean. A portion of seawater for dissolved species (D) was passed through a 0.2 μm Nuclepore filter and acidified to pH 2.2 with HCl and HF. A portion of seawater for acid-dissolvable species (AD) was acidified without filtration. Labile particulate (LP) species is defined as AD minus D, which represents a chemically labile fraction of particulate species. D-Zr, Hf and Ta increase with depth, Nb shows a slight depletion in surface water, whereas Mo and W have a conservative vertical profile. The concentration range of D-Zr, Hf, Nb, Ta and W is 31–275, 0.14–0.95, 4.0–7.2, 0.08–0.29 and 40–51 pmol kg⁻¹, respectively, whereas that of Mo is 97–105 nmol kg⁻¹. LP-species of Zr, Hf and Ta account for 10–14% of AD in average and increase up to 25% below 4000 m, whereas those for Mo and W are negligible. In contrast, LP-Nb shows maxima (up to 27%) in surface water. We also found that D-Zr/Hf, Nb/Ta and Mo/W mole ratios generally increase in the order continental crust < river water < coastal sea < open ocean.     

Basin-Scale Geographic Patterns of Bacterioplankton Biomass and Production in the Subarctic Pacific, July–September 1997

Bacterial biomass and production rate were measured in the surface (0–100 m) and mesopelagic layers (100–1,000 m) in the subarctic Pacific and the Bering Sea between July–September, 1997. Depth profiles were determined at stations occupied in oceanic domains including the subarctic gyres (western, Bering Sea, and Gulf of Alaska) and a boundary region south of the gyres. In the surface layer (0–100 m), both bacterial biomass and production were generally high in the western and Bering Sea gyres, with the tendency of decrease toward east. This geographic pattern was consistent with the dominant regime of phytoplankton biomass at the time of our survey. A significant portion of variation in bacterial production was explained by the concentration of chlorophyll a (r ² = 0.340, n = 60, P < 0.001) and, to the greater extent, by the concentration of semilabile total organic carbon (SL-TOC = TOC at a given depth—TOC at 1,000 m, r ² = 0.488, n = 59, P < 0.0001). Temperature significantly improved the regression model: temperature and chlorophyll jointly explained 60% of variation in bacterial production. These results support the hypothesis that bacteiral growth is largely regulated by the combination of temperature and the supply of dissolved organic carbon in subarctic surface waters. In the mesopelagic layer (100–1,000 m), the geographic pattern of bacterial production was strikingly different from the surface phytoplankton distribution: the production was high in the boundary region where the phytoplankton biomass was lowest. Bacterial growth appeared to be largely controlled by the supply of organic carbon, as indicated by the strong dependency of bacterial production on SL-TOC (r ² = 0.753, n = 75, P < 0.0001). The spatial uncoupling between surface phytoplankton and mesopelagic bacterial production suggests that the supply rate of labile dissolved organic carbon in the mesopelagic zone does not simply reflect the magnitude of the particulate organic carbon flux in the subarctic Pacific.