Deuterium abundance of natural waters

The deuterium abundance of natural water of various sources has been determined by the use of a deuterium mass spectrometer. The absolute deuterium contents of the reference sample nos. 1 and 1a of the U.S. National Bureau of Standards were found to be 0·0149 and 0·0128 mole % D₂O, respectively, by the comparison of the samples with the standard samples of known deuterium content. Relative enrichment of no. la to no. 1 (R_1a−R₁)/R₁×100 was 14·13 ± 0·23, which agrees perfectly to the value reported by . The variation of deuterium contents of tap waters of Tokyo and Osaka during last 2 years were within ± 1 per cent and any seasonal regularities could not be detected. Marine waters of the West Pacific have almost the same deuterium content as those of the Pacific coast of the United States. Marine waters at various depths of the Antarctic showed relatively large variation of deuterium content (from +0·84 to −1·16 per cent on the SMOW-scale), whereas the samples of Black Current of the Pacific showed little variation. It was found that the deuterium content of spring water suggests the origin of springs in some cases.     

Energy balance of the tidal current in the Obatake Seto Strait

Current measurements made with a Doppler Current Profiler were taken along cross sections in the Obatake Seto Strait, a small strait in the western part of the Seto Inland Sea.The energy loss between two cross sections of the strait was estimated using the control volume analysis of the stationary one-dimensional energy equation. The large energy loss observed in the strait cannot be explained in terms of general bottom friction in the coastal region. The loss is attributed to the form loss, which is accompanied by internal turbulence and vortices generated by the specific topography of the strait, in addition to the loss by friction. This is supported by the fact that the energy loss in the strait differs, depending upon the current direction.     

Abyssal circulation in the Japan Sea

Journal of Oceanography - The water below a depth of 1,000 m in the Japan Sea was found to consist of two water masses, the upper layer (the Deep Water) and the lower layer (the Bottom Water). The...     

Methane in the western North Pacific

The concentration of methane in about 400 seawater samples collected in the western North Pacific, mostly from 40°N to 5°S along 165°E was determined. While the concentration of methane in the surface water was slightly greater in the high-latitudes, it did not widely vary with a standard deviation of 0.29 n mol/l for a mean value of 2.49 n mol/l. The 90% confidence limit of the mean was 0.08 n mol/l. The degree of oversaturation in 1991 (31±4%) was not different from that in circa 1970. If we assume that this degree of oversaturation occurs in the entire oceans, the annual flux of methane becomes 6×10¹²g CH₄. Both the concentrations of methane and chlorophylla were higher in the surface 100 m layer. However, the correlation between them was not well in the entire surface waters. This may indicate that the production of methane is not directly related to the photosynthetic process. The concentration of methane decreased gradually with increasing depth down to 1000 m. Its horizontally and vertically uniform concentration in the abyssal water suggests that the turnover time of methane in the oxic pelagic water is in the range between a few years and a few hundred years.     

Lethality of increasing CO2 levels on deep-sea copepods in the western North Pacific

The first CO₂ exposure experiments on several species of pelagic copepods inhabiting surface and deep layers in the western North Pacific were conducted. Living organisms were collected from two layers between the surface and 1,500 m between latitudes of 11 and 44°N, and they were exposed aboard ship to various pCO₂ up to about 98,000 μatm. Mortality of copepods from both shallow and deep layers in subarctic to subtropical regions increased with increasing pCO₂ and exposure time. Deep-living copepods showed higher tolerance to pCO₂ than shallow-living copepods. Furthermore, deep-living copepods from subarctic and transitional regions had higher tolerances than the subtropical copepods. The higher tolerances of the deep-living copepods from subarctic and transitional regions may be due to the adaptation to the natural pCO₂ conditions in the subarctic ocean.     

Uptake of selenium and other oxyanionic elements in marine ferromanganese concretions of different origins

The concentration of selenium in marine ferromanganese concretions varies between 0.02 and 1.2 mg kg⁻¹, with an average of 0.6 mg kg⁻¹. This is about two orders of magnitude lower than previously reported. In contrast to minor cationic elements, the concentrations of selenium are relatively uniform between ferromanganese concretions of different origins, except for hydrothermal crusts. It shows the same trends of element enrichment as other oxyanionic elements. The incorporation of selenium into ferromanganese concretions is attributed to adsorption of selenate on iron and manganese oxides.     

Seasonal and areal variation of continental aerosol in the surface air over the western North Pacific region

Weekly aerosol samples were collected for two years from 1981 at six stations in the western North Pacific region. The samples were analyzed for aluminum to determine the mineral dust concentration in the air. By combining our data with observations in the central and eastern North Pacific by a US research group, the following results and conclusions have been obtained. Spring peaks in atmospheric mineral dust were observed at all the stations accompanied byKosa episodes (hazes due to mineral dust of Chinese origin). The spring peaks, however, varied from year to year. The mean concentration of mineral dust depends not only on the distance from the Asian coast but also on the latitude of the sampling station. The half-decrease distance of the atmospheric mineral dust turned out to be 500–600 km for all latitudes in the western North Pacific. This indicates that the rate of deposition of mineral dust in the western North Pacific is much larger than that in the central and eastern North Pacific.     

Barium Increasing Prior to Opal during the Last Termination of Glacial Ages in the Okhotsk Sea Sediments

Ba and Ti in a sediment core (10 m long) from the Okhotsk Sea, covering the last 120 kyrs, were measured. The authigenic Ba (Ba_ex) contents were calculated and compared with the opal. The correlation coefficient between Ba_ex and opal was quite small (r = 0.34), but it greatly grew larger (r = 0.90), if the Ba_ex contents were multiplied by a simple function increasing with depth, except for two intervals. This may be due to the gradual change in the sedimentation environment during the glacial ages. One of the exceptional interval is found at 60–170 cm in depth, corresponding to 10–17 calendar kyr ago, the last termination period of glacial ages, where the Ba_ex began to increase prior to opal. Since the calcium carbonate contents similarly increased prior to the opal increase, the Ba_ex may be also related to calcareous organisms besides siliceous ones. The other is the last interglacial period around 120 kyr ago when the opal contents were high, but those of the Ba_ex were not increased. This can be explained, if the Ba_ex was reduced to sulfide and dissolved away in a strongly anoxic environment during the biologically productive period. During the glacial ages, the mass accumulation rate (MAR) of lithogenic Ti was about twice the amount of that during the interglacial ages. For opal, however, the contrast between the glacial and interglacial ages was more remarkable in its MAR than in its concentration in sediments, due to the larger variation in the bulk sedimentation rates. This revised version was published online in July 2006 with corrections to the Cover Date.     

The Western North Pacific Playing a Key Role in Global Biogeochemical Fluxes

The oceanic biogeochemical fluxes in the North Pacific, especially its northwestern part, are discussed to prove their importance on a global scale. First, the air-sea exchange processes of chemical substances are considered quantitatively. The topics discussed are sea salt particles transported to land, sporadic transport of soil dust to the ocean and its role in the marine ecosystem, the larger gas transfer velocity of CO₂ indicating the effect of bubbles, and DMS and greenhouse gases other than CO₂. Next, chemical tracers are utilized to reveal the water circulation systems in the region, which are the Pacific Deep Water including its vertical eddy diffusivity, the North Pacific Intermediate Water and the Japan Sea Deep Water. Thirdly, the particulate transport process of chemical substances through the water column is clarified by analyzing the distribution of insoluble radionuclides and the results obtained from sediment trap experiments. Fourthly, the northern North Pacific is characterized by stating the site decomposing organic matter and Si playing a key role in the marine ecosystem. Both are induced by the upwelled Pacific Deep Water. Fifthly, the oceanic CO₂ system related to global warming is presented by clarifying the distribution of anthropogenic CO₂ in the western North Pacific, and roles of the upwelled Pacific Deep Water and the continental shelf zone in the absorption of atmospheric CO₂. Finally, Mn and other chemical substances in sediments are discussed as recorders of the early diagenesis and indicators of low biological productivity during glacial ages in the northwestern North Pacific. It is concluded that the western North Pacific is characterized mainly by the Pacific Deep Water bringing nutrients to the northern North Pacific, located at the exit of the global deep water circulation and, therefore, the region plays a key role in the global biogeochemical fluxes. This revised version was published online in August 2006 with corrections to the Cover Date.