Vertical distribution of heavy metals and its seasonal variations in Beppu Bay

From July to November, the thermocline which has strong temperature gradient (0.7C m^–1) is formed in the bottom water of Beppu Bay, and it prevents the downward mixing of surface water. This has caused the bottom water of the basin to become depleted in oxygen, and in November the bottom water below about 60 m depth becomes anoxic. Accordingly manganese and iron are reduced and more soluble under the anoxic condition, those concentrations are high relative to surface water, and the maximums are 1,240g l^–1 and 80g l^–1. Under the anoxic condition, the flux of dissolved manganese from the sediment is about 10g cm^–2 day^–1.     

The content and the oxidation state of arsenic and antimony in coastal water of Japan

The content and the oxidation state of arsenic and antimony in coastal seawater were determined coupled with chemical separation and neutron activation method. The contents of arsenic and antimony in coastal seawater were estimated to be 1.56–2.73g As/l, 0.25–0.57g Sb/l. Most parts of these elements exist as soluble ionic species, passing through 0.45 pore-size membrane filter, and at surface, 80–97% of arsenic occurs as arsenate and 70–94 % of antimony may occurs as antimonate. The vertical distribution of arsenite and arsenate is almost constant from the surface to 1,200 m depth. However the distribution of Sb(III) and Sb(V) is much more complicated with depth.     

Ammonium uptake kinetics and interactions between nitrate and ammonium uptake inChattonella antiqua

Ammonium uptake kinetics and interactions between nitrate and ammonium uptake were examined inChattonella antiqua. After the addition of ammonium to the culture ofC. antiqua, the ammonium concentration decreased linearly with time. The ammonium uptake rate as a function of ammonium concentration followed the Michaelis-Menten equation; the maximal uptake rate was 2.0 pmol cell^–1hr^–1 and the half saturation constant, 2.2M. Although the ammonium uptake was not affected by nitrate, uptake of nitrate was rapidly (15min) suppressed by ammonium and a 50% reduction in nitrate uptake was observed at an ammonium concentration ofca. 2M.     

Transport of copper from the Bering Sea to the northwestern North Pacific

Dissolved copper concentrations in surface waters of the Bering Sea ranged from 106 to 882 ngl^–1. Higher concentrations were found in continental shelf waters. In the northwestern North Pacific dissolved copper ranged from 54 to 140 ngl^–1. Particulate copper concentrations varied regionally and seasonally from 6 to 79 ngl^–1. Regionally averaged particulate copper concentrations decreased from 175 to 33g g^–1 against an increase in suspended materials because of the dilution effects of biological fractions. Apparent sporadic increases in copper concentrations were found in the mixing area of the Kuroshio and the Oyashio waters. The feature is attributed to the lateral distribution of different water types rather than to the upwelling of deeper waters by eddies. In the same area west of 160E, waters with high concentrations of dissolved copper (96±9 ngl^–1) were found. Their origin appears to be the continental shelf of the Bering Sea. In spite of intensive biological activity, a considerable fraction of copper added to shelf waters was transported to the area off Japan via the circulation in the Bering Sea and the Oyashio current.     

Gallium content in seaweeds

Analyses of gallium content were made by the fluorometric method on 57 samples of seaweeds which were composed of 30 species. As the result of it, the gallium content was found ranging from 0.02 to 0.64g g^–1 and the average was 0.14g g^–1 in the dried seaweeds.Generally, the gallium content in seaweeds had a close relationship to the aluminium and iron contents. The average weight ratio of Ga/Al was 3.8×10^–4 and one of Ga/Fe was 4.0×10^–4. The average Ga/Al weight ratio (3.8×10^–4) was very similar to that reported for shallow-water deposits (2.1×10^–4), but was definitely lower than that in sea water (1.5×10^–2).     

Respiration rates of copepod larvae and a ciliate from a tropical sea

The respiration rates of copepod larvae and a ciliate (Placus sp.) from a tropical sea were measured with an oxygen electrode method. The general range of body size of these animals was 40–161m (diameter equivalent to a sphere), and the respiration rate measured was 0.00076–0.00176l O₂ (animal)^–1h^–1 (or 2.02–9.05l O₂ (mg wet weight)^–1h^–1) at 25.5–29.2C. There was no marked difference observed between the respiration rates of copepod larvae and the ciliate. The respiration rates obtained here are relatively higher than the rates of other similar sized protozoans found in the literature, but lower than the rate extrapolated from larger planktonic copepods in tropical seas.The present results and other information available on microzooplankton biomass suggest that microzooplankton respiration is of near equal importance to that of net zooplankton in the study of energy flow through tropical, pelagic ecosystems.     

Radiation balance and heat budget at the ocean/atmosphere interface in the western North Pacific

The downward short- and long-wave radiation fluxes at the sea surface (S, L) were measured aboard the R/VHakuho Maru, University of Tokyo, for the period of 117 days on six cruises from 1981 to 1985 in the western North Pacific near Japan. The upward fluxes of short- and long-wave radiation (S, L) were calculated by Payne's (1972) table and the Stefan-Boltzmann's law, respectively. The sensible and laten heat fluxes (Q _h ,Q _e ) were also estimated from an aerodynamic bulk method.From April to August, the daily mean value ofS varied with the amplitude of 100200 Wm^–2. The value ofS was estimated approximately 6% ofS in all seasons. The difference betweenL andL was so small that the net radiation flux (Q _n ) was dominated byS. In addition, the net heat flux at the sea surface was also dominated byS due to small values ofQ _h andQ _e , and then the ocean was warmed at the rate of 111 Wm^–2 in April and 63 Wm^–2 in August in the Oyashio Area, and 132 Wm^–2 in May and 164 Wm^–2 in June in the Kuroshio Area, respectively.From September to March, a remarkable negative correlation between the day to day variation ofS and that ofL was observed except when an intense cold air outbreak occurred. It was found that the correlation was caused by the cloud climatological feature of the western North Pacific in this period.S was not a dominant factor in the net heat flux. The value ofQ _h +Q _e in the Kuroshio Area ranged from 260 Wm^–2 to 630 Wm^–2, much larger thanQ _n which ranged from –8 Wm^–2 to 92 Wm^–2 in the leg mean values (each leg period was about 10 days). Then the ocean was cooled at the rate of –160–620 Wm^–2 during this period. The net heat flux in the Kuroshio Area averaged over five legs from late November to February was –473 Wm^–2. This value is 50100% larger than the climatological values reported so far.The temporal and spatial variability of radiation fluxes and heat fluxes during each leg was also discussed.     

Chlorinated hydrocarbons in the North Pacific and Indian Oceans

PCBs, DDT compounds and HCH isomers were detected in the air and surface waters of the North Pacific and Indian Oceans, including the Bering Sea, East China Sea, South China Sea, Bay of Bengal and the Arabian Sea. The general concentrations of each chlorinated hydrocarbon were as follows: water PCBs 0.1 to 1.0, DDT 0.01 to 1.0, HCH 1.0 to 10 ngl ^–1; air DDT 0.01 to 1.0, HCH 0.1 to 10 ng m^–3. PCB concentrations in surface waters were slightly lower than those of the North Atlantic and North Sea previously reported, while DDT concentrations in the air and water were higher. Remarkably high concentrations of DDT and HCH were found in the air off the western coast of India. Also in the Pacific site off Central America, a fairly high concentration of DDT was observed in an air sample. These data suggest that large amounts of DDT and HCH are being used in the tropical zone, especially in southern Asia. Furthermore, high concentrations were observed both in the air and water of the Northwest Pacific between 30°N and 40°N latitude. There is a possibility that both pesticides are not only still being used in lower latitude countries but also in the mid-latitude ones of the Asian continent excluding Japan. In addition to this atmospheric circulation may also contribute to the concentration of these pesticides in the mid-latitudinal zone.     

Benzo(a)pyrene in the sediment of Osaka Bay and Keihin Canal and its estimated sources

Benzo(a)pyrene (BP) in the sediment of Osaka Bay were determined. High concentration was found at two stations near the mouth of Shin-Yodo and off Kobe respectively (0.98g g^–1 dry mud basis, 1.1g g^–1). The concentration decreases regularly from the mouth of the river further into the bay. The other supplemental determination was carried on the sediment and the seawater of Keihin Canal. Notable BP concentration of 89g g^–1 was observed in the sediment beneath the effluent outlet of a gasworks. The BP in the sediment near the ironworks was also considerable, while the BP was relatively less in the sediment beneath the effluent outlet of refineries. These data suggest that coke plants working in gasworks or ironworks may be the larger sources of BP than refineries. The results of Osaka Bay coincide with this hypothesis.Cadmium, lead, copper, zinc, nickel, ignition loss and fine sand content were measured from the same sediment samples of Osaka Bay. Cd, Pb, Cu and ignition loss showed the regular distributions which resemble to BP and accordingly, good correlations with BP. No significant correlations were found between BP and Ni, Zn and fine sand content which showed no regular distributions.     

Light scattering and suspended particulate matter in the Arctic Ocean north of Ellesmere Island

Light scattering profiles and water samples for filtration of suspended particulate matter were obtained during fall, 1973, from Ice Island T-3, then located about 50 miles north of Ellesmere Island. The profiles reveal almost no variability in scattering, either in the water column, or in time during our two weeks of field work. Gravimetric analysis of the filtered suspended particulate matter shows that mass concentrations are low, averaging about 7g l^–1, and that they too remain very constant. The four water masses present in the Arctic Ocean could not be distinguished by our observations of light scattering and mass concentration of suspended particulates.     

Rates of net assimilation and respiration of amino acids by marine bacteria

The selectivity of amino acid assimilation by marine bacteria was examined using seven kinds of¹⁴C-amino acids and the acid hydrolysate of¹⁴C-labelled proteins. It was found that the net assimilation and respiration by marine bacteria followed MICHAELIS-MENTEN kinetics for all of amino acids used in our experiments. Maximum velocities of amino acids were 0.01 to 0.19g carbon/hour per 2×10⁷ cells for net assimilation and less than 0.18g carbon/hour per 2×10⁷ cells for respiration at 20C. The velocity of gross assimilation was found with the following order: phenylalanine>valine, glutamic acid>serine, arginine>tryptophan>glycine. The assimilation velocities of amino acids in these laboratory works showed almost the same order as those in field experiments. The assimilation velocity of an amino acid was influenced by coexisting another amino acids or glucose. The assimilation velocity in lower substrate range of amino acids was directly proportional to the number of bacterial cells in the range from 6×10² to 3×10⁴ cells per ml. No linear relation between the assimilation velocity of amino acids and reciprocal of absolute temperature was found, but a marked bending was observed at 15 to 20C. The velocity at the optimum temperature was three to six times of that at 5C.     

The content of selenium and its chemical form in sea water

By using the new fluorometric method of determination of the total selenium ( Se), Se (IV) and Se (VI), the content of selenium in sea weter was determined in the western North Pacific. Results showed that the content of Se in surface water ranged from 0.06 to 0.12g l^–1, while in deeper layers, the content increased to 0.20g l^–1. It was found that Se (IV) showed rather uniform distribution with depth, while Se (VI) increased with depth to about three times that in the surface. The ratio of Se (IV) to the Se ranged from 0.5 to 0.8 in the surface and 0.4 to 0.6 in the deep. The coexistence of the hexa- and tetravalent ions of selenium was confirmed both in surface and deep layers. Some results of observations on the content of selenium in the coastal areas of Japan were also reported.     

Bispectra of spike-array type time series and their application to the analysis of oceanic microstructures

Bispectral analysis is applied to records of the vertical profile of the vertical temperature gradient in the oceanic thermocline in the San Diego Trough. The bispectra exhibit three notable features; (1) bispectral peaks at the points (0.2 m^–1, 0.2 m^–1) and (0.2 m^–1, 0.1 m^–1), (2) bispectral ridges along the lines ( ₁= ₀, ₂= ₀ and ₁+ ₂= ₀ corresponding to peak wavenumbers ₀ in power spectra, and (3) array of bispectral peaks of interval of 0.2 m^–1 The results are compared with the bispectra of several modeled time series of spike-array type. The periodicity of 5 m found in the records seems to have two meanings: spacing of predominant spikes and wavelength of predominant sinusoidal wave. If this indicates the existence of internal waves having a vertical wavelength the same as the scale of homogeneous layers, it would suggest the possible importance of internal waves in the formation and maintenance mechanisms of oceanic microstructure.     

Differential sorption of organic matter by various sized sediment particles in recent sediment from the bering sea

A recent unconsolidated marine sediment collected from the Aleutian basin of the Bering Sea (5702.9N, 17657.4W) was separated into eight size fractions by sieving. Each of the fractions was analyzed for density, organic carbon, total nitrogen and various organic materials. A detailed analysis of the correlation of organic carbon and total nitrogen to the mean diameter of the particles separated, indicated that the surface sorption processes of organic matter were the determinative factor controlling the concentration of organic carbon and total nitrogen on silt and clay particles of the sediments.Selective sorption of amino acids was found to occur in the 8–20 and 5–8m. fractions of the sediment. This is assumed to be due to their surface active property.     

Mineralogical study of the core samples from the Indian Ocean,with special reference to the vertical distribution of clay minerals

The clay minerals in the 18 core samples collected from the northern, equatorial and southeastern Indian Ocean are illite, chlorite, montmorillonite and kaolinite. In the fraction finer than 2 in the surface layer (top to 5 cm deep) of each core, the relative abundance of clay minerals varies widely from area to area. Kaolinite possesses the maximum proportion of the clay mineral composition and chlorite has the minimum proportion.Kaolinite is particularly dominant in sediments near off the northwestern coast of Australia. In the factions finer and coarser than 2 of the surface layer, montmorillonite and kaolinite tend to be abundant in the fraction finer than 2, and chlorite and illite tend to be abundant in the fraction coarser than 2. In some cores, kaolinite-rich layers in sediments which are considered to have been transported by turbidity currents from the Bay of Bengal are found. Turbidity currents appear partly a role in transport of sediments to the equatorial Indian Ocean.As to the relation between the vertical change of clay mineral composition and geochronological data, montmorillonite and kaolinite tend to be more abundant in interglacial ages than in glacial ages, while illite and chlorite tend to exhibit opposite trend.Muscovite and biotite highly concentrated in the cores Ka-9 and Ka-15 collected from the equatorial Indian Ocean seem to originate from granite or gneiss of Ceylon and/or India.     

Glacial to Holoceneδ 13C variations in intermediate depth water masses of North Indian Ocean

The ¹⁸O and ¹³C compositions of glacial- to Holocene-aged benthic foraminifera in a core collected from the eastern Arabian sea (water depth 1230 m) were determined to investigate glacial—interglacial variations in the intermediate depth water chemistry of the North Indian Ocean. In addition, we determined the ¹³C composition of Holocene benthic foraminifera from seven cores for which the ¹⁸O and ¹³C of benthic foraminifera from last glacial maximum (LGM) were reported by Kallel et al. (1988). The ¹³C_DIC in the intermediate waters was generally depleted by 0.3–0.4 during the last glacial maximum compared to Holocene.     

Enrichments in Hg,Cd, As,and Sb in recent sediments of Azores-Iceland Ridge

Mercury, cadmium, arsenic, and antimony were analyzed in cores sampled on the Azores-Iceland Ridge. High values of 780 g · kg^–1 for Hg, 1.7 g · g^–1 for Cd, 87 g · g^–1 for As, and 8.1 g · g^–1 for Sb occur in the rift valley and transform faults. These enrichments, strictly linked to the ridge, could not have an allochtonous origin. A local hydrogenous flux may explain this phenomenon. These metallic enrichments may be connected to a hydrothermal activity extended between 43° N and 47° N.     

Geophysical and geochemical observations on actively seeping hydrocarbon gases on the south-eastern Yellow Sea continental shelf

In the southeastern Yellow Sea, active seepage of hydrocarbon gases has been observed by high-resolution (3.5 kHz) seismic profiling both in 1987 and 2001, occurring through a large number of plumes from the topmost pre-Holocene sedimentary layer. It is strong enough to compensate for current speed, extending vertically up to the sea surface. The gas seepage often appears to be explosive to form craters and diapirs, although pockmarks are rare due to the redistribution of mobile palimpsest sands. In core-top seawater and sediments, the gases are characterized by high amounts of C₂, homogenous ¹³C₁ values and a large difference (19.7 on average) between ¹³C₁ (–55.2 to –53.6 PDB) and ¹³C₂ (–36.8 to –32.5 PDB) values. The gases are considered to be generated with a smaller amount of C₁ at the early thermal cracking stage of labile source materials, after which the C₂ gas is enriched in ¹³C by diffusion or biological alternation at the generation or accumulation site. The homogenous ¹³C₁ values may be one of the geochemical characteristics of gases acquired at depth which are less altered in the case of rapid diffusive gas migration to the seafloor.     

Alkylbenzenesulfonate (ABS) in the bottom muds of the inner part of Tokyo Bay

The contents of alkylbenzenesulfonate (ABS) in the bottom sediments were analyzed for the inner part of Tokyo Bay and five inflowing rivers. Methylene blue active substances (MBAS) was extracted from the dired sample with methanol-benzene mixture.After the concentration of MBAS was determined by colorimetry, the ratio ABS/MBAS was estimated by an infrared spectrum of MBAS-MB complex. The net content of ABS was calculated from these two values.The ABS contents in the surface of the bottom sediments of the rivers and sea ranged 1.959g/g and 014.1g/g dry weight, respectively. The contents of ABS in the river sediments reflected the degree of pollution of each river by urban waste waters. From the results of the analysis of the core samples of sea sediment at two points containing ABS only in the upper layer, the average rate of sedimentation of the bottom muds in the inner part of Tokyo Bay since the usage of ABS began was estimated as 3 cm/year and 7 cm/year respectively.     

A field study of physico-chemical states of artificial radionuclides in seawater

The physico-chemical states of artificial radionuclides,⁹⁰Sr,¹³⁷Cs and¹⁴⁴Ce in seawater were investigated by radiochemical analysis of filtered and unfiltered seawater. The difference of radionuclide concentrations between unfiltered and filtered seawaters was defined as the particulate form radioisotope and its particle ratio was discussed.Practically no particulate⁹⁰Sr, greater than 0.22 in size, was observed in both coastal and open seawaters, but some of¹³⁷Cs seemed to be insoluble in some circumstances, especially in coastal waters. A considerable amount of¹⁴⁴Ce was found to be particulate.An estimation of the radionuclides in particulate form was made for Kashima-nada seawaters collected in 1970 to 1972, and it was shown that the possible occurrence of particulate radionuclides, greater than 0.22 in size, were 1% or less for⁹⁰Sr and 6% for¹³⁷Cs. In the coastal water, 80 % of¹⁴⁴Ce were seemed to be in particulate form, but in the open seawater only a few%. The influences of suspended materials to¹³⁷Cs and¹⁴⁴Ce concentration levels in seawater were not negligible and further investigations are desirable.