Concentration and Regeneration of Cd in the Japan Sea Proper Water

The concentration level of cadmium (Cd) and the regeneration related to phosphate (PO₄) were examined at two stations (CM10, CM12) in the eastern Japan Basin in July 1998. The observed Cd concentrations were around 0.2–0.3 nM and 0.5–0.6 nM in the surface and deep layers (Japan Sea Proper Water; JSPW), respectively; the concentration of Cd in the JSPW was much lower than that in the Pacific deep water, which is attributed to its specific formation system (which driven by the winter convection of the surface layer within the Japan Sea, thereafter descending to the deep layer) connected with the relatively active vertical mixing in the Japan Sea. A plot of Cd against PO₄ showed good linearity with positive y-intercept values, suggesting that the excess Cd was apparently not available in the biogeochemical cycle. The molecular ratios of consumed O₂ to regenerated Cd and PO₄ in the JSPW were 688,000, 140 and 881,000, 146 for CM10 and CM12, respectively, and a lower preformed Cd concentration (around 0.37 nM) was also estimated in the JSPW, different from that of the North Pacific deep water (613,000 for Cd, 170 for PO₄, and 0.64 nM of preformed Cd).     

Preformed Cd and PO4 and the relationship between the two elements in the northwestern Pacific and the Okhotsk Sea

Preformed Cd and PO₄ were investigated in the northwestern Pacific (Station CM05) and the Okhotsk Sea (Station CM06), and the relationship between the two elements was examined. At CM05, from the apparent oxygen utilization (AOU)–Cd and PO₄ plot, the different molecular ratios of consumed O₂ to regenerated Cd and PO₄ were calculated to be 254,000 (Cd) and 96 (PO₄) for the shallow layer (30–99 m) and 613,000 (Cd) and 170 (PO₄) for the deep layer (below the oxygen minimum layer), which suggested the preferential remineralization of Cd and PO₄ in the shallow layer. At CM06, regeneration ratios of O₂/Cd, PO₄ were obtained only in the shallow layer (29–124 m) as 227,000 (Cd) and 75 (PO₄). The calculated preformed Cd and PO₄ concentrations in the shallow layer were 0.59 nM of Cd and 1.6 μM of PO₄ at CM05 and 0.35 nM of Cd and 0.95 μM of PO₄ at CM06. These concentrations were much higher than those (close to 0) in the low-latitude area, which was attributable to the supply of these constituents from deep water by the strong winter convection. In the deep layer, at CM05, preformed concentrations were 0.64 nM of Cd and 1.4 μM of PO₄. Preformed PO₄ generally agreed with previously reported values in the Pacific, which suggested that the concentrations of the initial PO₄ in the deep water were preserved as preformed through the movement to the northwestern Pacific. On the other hand, obtained preformed Cd in the northwestern Pacific deep water showed a somewhat higher value than that in the southwest Pacific. The possibility of the terrestrial input and remineralization of Cd by CaCO₃ dissolution during the northward movement was considered. A plot of Cd and PO₄ showed a linear relationship with slopes of 0.34 and 0.40 (nM/μM) at CM05 and CM06, respectively, which generally agreed with the reported values in the North Pacific.     

Relationship between Cd and PO4 in the Subtropical Sea near the Ryukyu Islands

The relationship between dissolved cadmium (Cd) and phosphate (PO₄) was examined at three stations in the subtropical area near the Ryukyu Islands in May 1999. Preformed PO₄ was obtained using the Redfield ratio in order to separate the surface water and the other layers in this study area. Almost 0 μM (−0.043 μM to 0.094 μM) was estimated in the layers above 300 m and 250 m at Sts. 1 and 3 and at St. 2, respectively. Up to these depths, water was considered to be uniform, and these layers were defined as the surface water in this study area. In the surface water, the slopes of the regression lines of the Cd-PO₄ plot were 0.162, 0.156, and 0.226 (nM/μM) at Sts. 1, 2, and 3, respectively, and these values were much closer to the estimated regenerated ratio of Cd to PO₄ from the Apparent Oxygen Utilization (AOU)-Cd/PO₄ plots, which was 0.197 (nM/μM) in this study area. Below surface layers, the slopes of the Cd-PO₄ plot changed to 0.371, 0.352, and 0.362 (nM//μM) at Sts. 1, 2, and 3, respectively. In the relationships between Cd and PO₄, clear deviations or kinks were observed at three stations at a PO₄ concentration of approximately 0.2 μM in the plot, which was attributable to the discontinuity of surface water and the other layers across the North Pacific subtropical mode water. In studies of the interaction between surface water and biogenic particles concerning the Cd/PO₄ ratio, separate analyses of seawater (surface water and the other layers) should be carried out to obtain the individual surface water ratio because the Cd/PO₄ ratio in the surface water is expected to differ from that of the underlying water. Furthermore, the biological fractionation of these constituents is based on the surface water ratio. This revised version was published online in July 2006 with corrections to the Cover Date.     

Relationship between cadmium and phosphate in the northwest Pacific Ocean

The relationship between Cd and PO₄ in the Kuroshio and Oyashio regions and the Okhotsk Sea was examined. The resultant equations are as follows: Cd (ng l^–1)=37.0 PO₄ (M)+2.6; Cd(ng l^–1)=32.1 PO₄ (M)+1.2 and Cd (ng l^–1)=34.1 PO₄ (M)+7.9, respectively. These results are in good agreement with previously reported studies, and indicate that during removal from surface waters to deeper waters by biological assimilation and regeneration in deeper waters Cd and PO₄ maintain the same ratio in the open ocean. The relationship between Cd and PO₄ in coastal waters, however, differed from that in the open ocean.     

Cadmium, copper and nickel distributions at four stations in the eastern central and south Atlantic

Distributions of cadmium, copper and nickel at four stations in the eastern part of the Atlantic Ocean from 30 ° S to 34 ° N are described based on analytical results from three laboratories. The Cd and Ni profiles show nutrient-like distributions with concentrations in the deep waters increasing from north to south. Copper profiles all show gradual increases from surface to bottom with the highest concentrations occurring near bottom on the most northerly station.Variations in the deep-water Cd and Ni concentrations can be understood in terms of mixing of southern source waters with high concentrations with lower concentration northern source waters. The deep-water Cu distributions indicate a significant near-bottom source to the northern end of the section.Cadmium vs. phosphate relationships show features that result from both regeneration and mixing. Higher Cd:PO₄ ratios are seen in the southern source waters than in the northern waters, thus discounting the suggestion that the inflection in the global Cd:PO₄ relationship at PO₄ ≈ 1.3 μM originates in the southern ocean. Differential regeneration of Cd and PO₄ is seen through the equatorial oxygen minimum.     

Contrasting oceanographic conditions and phytoplankton communities on the east and west coasts of Australia

The composition and dynamics of the phytoplankton communities and hydrographic factors that control them are described for eastern and western Australia with a focus on the Eastern Australian Current (EAC) and Leeuwin Current (LC) between 27.5° and 34.5°S latitude. A total of 1685 samples collected from 1996 to 2010 and analysed for pigments by high performance liquid chromatography (HPLC) showed the average TChla (monovinyl+divinyl chlorophyll a) concentration on the west coast to be 0.28±0.16 ??g L⁻¹ while it was 0.58±1.4 ??g L⁻¹ on the east coast. Both coasts showed significant decreases in the proportions of picoplankton and relatively more nanoplankton and microplankton with increasing latitude. On both coasts the phytoplankton biomass (by SeaWiFS) increased with the onset of winter. At higher latitudes (>27.5°S) the southeast coast developed a spring bloom (September) when the mean monthly, surface chlorophyll a (chla) concentration (by SeaWiFS) was 48% greater than on the south west coast. In this southern region (27.5-34.5°S) Synechococcus was the dominant taxon with 60% of the total biomass in the southeast (SE) and 43% in the southwest (SW). Both the SE and SW regions had similar proportions of haptophytes; ∼14% of the phytoplankton community. The SW coast had relatively more pelagophytes, prasinophytes, cryptophytes, chlorophytes and less bacillariophytes and dinophytes. These differences in phytoplankton biomass and community composition reflect the differences in seasonality of the 2 major boundary currents, the influence this has on the vertical stability of the water column and the average availability of nutrients in the euphotic zone. Seasonal variation in mixed layer depth and upwelling on the west coast appears to be suppressed by the Leeuwin Current. The long-term depth averaged (0-100 m) nitrate concentration on the west coast was only 14% of the average concentration on the east coast. Redfield ratios for NO₃:SiO₂:PO₄ were 6.5:11.9:1 on the east coast and 2.2:16.2:1 on the west coast. Thus new production (nitrate based) on the west coast was likely to be substantially more limited than on the eastcoast. Short term (hourly) rates of vertical mixing were greater on the east coast. The more stable water column on the west coast produced deeper subsurface chlorophyll a maxima with a 25% greater proportion of picoeukaryotes.     

Inferring upwelling rates in the equatorial Atlantic using Be measurements in the upper ocean

Ocean upwelling rates are difficult to measure because of the relatively small velocities involved, and therefore are typically inferred from indirect methods such as heat budget estimates or tracer observations. Here we present the first results using a novel technique, based on the isotope ⁷Be, to infer rates of upwelling along the equator. Beryllium-7 (half-life=53.3 d) is a cosmic-ray produced radioactive nuclide that is deposited by rainfall upon the ocean surface and subsequently enriched and homogenized within the mixed layer. Previous investigations have utilized the penetration of characteristically high mixed layer concentrations into the upper thermocline to trace ocean ventilation and subduction over seasonal timescales. Here, the tracer is used in a reverse sense; that is, the ⁷Be concentration in the usually ⁷Be-rich surface mixed layer will be diluted from penetration of ⁷Be “dead” water upwelled from below. This dilution provides a means to infer upwelling rates. Furthermore, with knowledge of upwelling rates, ⁷Be profiles can be used to constrain vertical diffusivity within the upper thermocline. These ideas were tested with samples collected during the Tropical Atlantic Climate Experiment (TACE) cruise (May 22-June 27, 2009). The observations indicated a nearly linear relationship between ⁷Be inventory and mixed layer temperature, as with increased upwelling, lower mixed layer temperatures correspond to greater ⁷Be dilution from depth. With this data, upwelling rates were estimated at a number of stations near the equator between 0°E and 30°W within and adjacent to the equatorial cold tongue. The derived upwelling rates ranged from 0 to 2.2 m/d, with maximum values found between the equator and 2°S. The corresponding K_z values derived for the upper thermocline were in the range 1-4×10⁻⁴ m²/s.     

Trace metals in the Western Pacific: temporal and spatial variability in the concentrations of Cd, Cu, Mn and Ni

Profiles of total dissolvable Cd, Cu, Mn and Ni are reported for samples collected from the southwest Pacific in 1989, from the western equatorial Pacific along 155°E at 5°S, 0° and 5°N in 1990 and 1993, and along the equator from 143°E to 152°E and in the Bismarck Sea in 1997 and 2000. Profiles of Cd along 155°E in 1990 and along the equator were essentially the same but, in 1993, Cd values at 5°N were higher by a factor of about 1.5–2 than at 5°S over the depth range 500–1500 m. Similar, but less pronounced, differences were observed for PO₄ and Ni. Cd and Ni were both strongly correlated with PO₄, and an even stronger correlation was found between Ni and Cd. The concentration of Ni did not fall below ≈2 nmolkg⁻¹, even in the nitrate-depleted waters of the western equatorial Pacific, where primary production is strongly dependent on recycled nitrogen (mainly ammonia and urea). It is proposed that this residual Ni is not bioavailable and that Ni could be biolimiting, since the metabolism of urea requires the nickel-containing enzyme urease. The impact of the Sepik River on Cd, Cu and Ni concentrations was small but elevated concentrations of Mn were observed near the Sepik River and close to the coast suggesting that the rivers and sediments on the north coast of New Guinea are a significant local source of Mn to the Bismarck Sea. Simple mass balance calculations show that the elevated levels of Mn observed in the Equatorial Undercurrent cannot be due to input from the rivers of New Guinea and they were attributed to the trapping of particulate matter due to strong current shear. A strong hydrothermal source of Mn was observed in the central Bismarck Sea.     

Cadmium and phosphate in coastal Antarctic seawater: Implications for Southern Ocean nutrient cycling

Cadmium is a biologically important trace metal that co-varies with phosphate (PO₄³⁻ or Dissolved Inorganic Phosphate, DIP) in seawater. However, the exact nature of Cd uptake mechanisms and the relationship with phosphate and other nutrients in global oceans remain elusive. Here, we present a time series study of Cd and PO₄³⁻ from coastal Antarctic seawater, showing that Cd co-varies with macronutrients during times of high biological activity even under nutrient and trace metal replete conditions. Our data imply that Cd/PO₄³⁻ in coastal surface Antarctic seawater is higher than open ocean areas. Furthermore, the sinking of some proportion of this high Cd/PO₄³⁻ water into Antarctic Bottom Water, followed by mixing into Circumpolar Deep Water, impacts Southern Ocean preformed nutrient and trace metal composition. A simple model of endmember water mass mixing with a particle fractionation of Cd/P (α_Cd–P) determined by the local environment can be used to account for the Cd/PO₄³⁻ relationship in different parts of the ocean. The high Cd/PO₄³⁻ of the coastal water is a consequence of two factors: the high input from terrestrial and continental shelf sediments and changes in biological fractionation with respect to P during uptake of Cd in regions of high Fe and Zn. This implies that the Cd/PO₄³⁻ ratio of the Southern Ocean will vary on glacial–interglacial timescales as the proportion of deep water originating on the continental shelves of the Weddell Sea is reduced during glaciations because the ice shelf is pinned at the edge of the continental shelf. There could also be variations in biological fractionation of Cd/P in the surface waters of the Southern Ocean on these timescales as a result of changes in atmospheric inputs of trace metals. Further variations in the relationship between Cd and PO₄³⁻ in seawater arise from changes in population structure and community requirements for macro- and micronutrients.     

Nutrients in an oligotrophic boundary current: Evidence of a new role for the Leeuwin Current

New observations along the continental shelf of Western Australia provide a novel explanation for the established ∼60 years relationship between Leeuwin Current (LC) strength and greater winter nitrate concentrations at 32°S plus the inter-annual variation in the magnitude of the annual, shelf-scale, phytoplankton bloom. The potential source of dissolved nitrogen to support the annual shelf scale phytoplankton bloom was identified as thin layers of an unprecedented areal extent, nitrate concentration and shallow nature that were observed off the northwest of Australia. We propose that the dissolved inorganic nitrogen (DIN) in these layers enters the LC at depth and then enters the euphotic zone via by three mechanisms: instability that results in a warm core eddy, cooling that deepens the surface mixed layer and shallowing of the thin layer. During the onset of the annual phytoplankton bloom along the west coast of Australia from 22°S to 34°S the poleward flowing LC was clearly evident as a surface intensified ocean boundary current transporting warmer, lower-salinity, greater-silicate waters in a shallow mixed layer rapidly southward. Between 24 and 26°S the core of the LC was present as a 50–100 m deep layer over one or more thin layers, 15–50 m thick, with high nitrate and low dissolved oxygen (DO). These layers were of lower salinity, cooler water with markedly reduced DO, high nitrate concentrations and distinct nitrate:silicate (NO₃:Si(OH)₄) nutrient ratios. As the LC flowed south it cooled and deepened thereby entraining the thin layers of high nitrate water into the euphotic zone. The LC also formed large (greater than 100 km diameter) warm core eddies with a deep surface mixed layer that also entrained nitrate from these thin layers. In some locations as far south as 32°S the LC was still present with the thin layer of high nitrate intact but now within the euphotic zone. Thus, the available evidence suggests the LC arises under conditions that favour rapid and shallow nitrification. This nitrification fuels a shelf-scale bloom on a downwelling favourable coast. Depending upon the rate of nitrification the source of the particular organic matter may be local or delivered from the tropics via horizontal advection in a subsurface layer of the LC.     

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.     

Chlorophyll distribution and photosynthetic activity in the north and equatorial Pacific Ocean along 155°W

The distribution of chlorophylla and photosynthetic characterestics of phytoplankters were investigated along 155°W between 50°N and 15°S during the KH-69-4 cruise of the R. V. Hakuh Maru (Aug. 12–Nov. 13, 1969). High concentrations of chlorophylla (more than 0.2 mg Chla/m³) were observed above the depths of 150 m at all stations except in 17°N, 5°S and 15°S. North of 20°N, the depths of chlorophyll accumulation shifted from near the surface to 50–100 m with southwards. In the equatorial region, chlorophyll accumulation centered at a depth of about 70 m and ranged vertically between 10 and 150 m. In all cases in the present study area, chlorophyll accumulation occurred within the euphotic zone (above the depth corresponding to 1% of the surface illumination), and except in the subarctic and some equatorial waters, this was usually prevalent in the lower half of the euphotic zone.The photosynthetic activities (initial slope of P vs I curve) of samples from the depths of chlorophyll accumulation were similar to, or lower than, those of shallow samples from the depths of upper half of the euphotic zone. At the depths of chlorophyll accumulation, calculatedin situ photosynthesis was high in the central Pacific and equatorial waters but low in the subarctic waters.     

大规模增养殖区柘林湾叶绿素a的时空分布

柘林湾是粤东一个大规模海水增养殖区和赤潮重灾区.2001年7月至2002年7月对柘林湾及其周边水域(共设19个站位)进行的叶绿素a含量周年调查结果表明,调查海区叶绿素a站位实测值年变化为0.01~3.26 mg/m3,均值为0.56 mg/m3.平面分布的基本格局表现为湾顶黄冈河内与湾口外侧海域的叶绿素a含量明显高于湾内的,湾内外侧和东部水域的叶绿素a含量明显高于湾内内侧和湾西部的.结合同步调查的水化数据得知,柘林湾是一个高营养盐、低叶绿素的海湾,其原因可能与高密度、大规模海水增养殖业引起的水流不畅、水下光照减弱和养殖贝类的摄食等有关.柘林湾叶绿素a含量的季节变化显著,最高值出现在2001年夏季8月,最低值出现在冬季1月和2002年7月,其中2002年7月的叶绿素a含量仅为2001年7月的1/10左右.这种巨大的年际间变化显然与2001~2002年厄尔尼诺现象导致粤东地区于2002年春夏期间气候异常、干旱少雨、径流剧减和调查海区浊度大幅升高有关.     

Modelling trace metal concentration distributions in estuarine waters

The concentration of dissolved organic carbon (DOC) was measured every few months from September 2000 through October 2001 at a coastal location in the center of Suruga Bay, Japan (34°51′N, 138°38′E). Water samples were collected three times per day (midday, night and predawn). DOC concentrations ranged from 91.3 to 45.2 μM C on the surface to 100 m depth. Diel variation in DOC concentrations, among the three sampling times, was greater in the upper 20 m, with a maximum difference of 21.7 μM C in July 2001, and reflected in diel DOC inventory variations from the surface to 50 m. Diel variations were controlled by both physical and biological factors. DOC concentrations were significantly correlated with potential density in the deeper layers (100–1000 m), indicating that the distribution of DOC concentrations in the deeper layer was mainly due to mixing. Most DOC concentrations in the upper layer (0–50 m) did not display the same relationship as in the deeper layer. Using the relationship with potential density at 100–1000 m, the DOC concentration in the upper layer, due simply to mixing, was calculated. The difference between the calculated and observed DOC was used to estimate biological contribution. The biological contributions to the DOC inventory in the upper layer (0–50 m) were found greatly in November 2000 and April 2001. This indicates that excess DOC accumulated, by biological processes, in the upper layer during these periods. In November 2000, the excess DOC in the inventory was constant throughout the sampling days (0.36–0.37 mol C m⁻²), whereas diel variations of DOC in the vertical profile were large and contrary to the variation between 10 and 20 m. This suggests that the excess DOC was contributed biologically during daytime in the uppermost layer and reached to the 50 m depth by deeper mixing. As a result, the inventory appeared to be stable over a day because of the compensating effects of DOC production and consumption throughout 50 m. In contrast, in spring and summer, there was a distinct diel inventory decrease in the nighttime, with apparent rates ranging from −0.61 to −0.35 μM C h⁻¹. It is probable that the DOC, which accumulated during the daytime, was mostly labile, with a turnover time of a few hours. The results indicate that the dynamics of diel DOC variations varied seasonally, and suggest that these variations need to be considered when estimating seasonal DOC pools in the coastal ocean.     

Trace metals (Co,Ni, Cu,Cd, and Pb) in the southern East/Japan Sea

Total dissolvable metals (Co, Ni, Cu, Cd, and Pb) in both surface waters and the water columns were acquired in the southern East/Japan Sea during a cruise around the Ulleung Basin in June 2001 to understand the spatial distributions of the metals. Concentrations in offshore surface waters were found to be Co 60 ± 12 pM, Ni 2.16 ± 0.25 nM, Cu 1.85 ± 0.55 nM, Cd 0.134 ± 0.018 nM, and Pb 155 ± 40 pM. Spatial distributions in surface waters showed that metal levels were generally enhanced at coastal sites in both Korea and Japan, where the metal distributions indicated complex patterns due to inputs, biogeochemical processes, and physical factors including upwelling. The Co distributions in the water columns seemed to be influenced predominantly by surface and bottom inputs, scavenged rather than regenerated at depth. For Cd, there was generally good agreement between the Cd and PO₄ depth distributions, in agreement with the literature. The Cd/PO₄ ratio from the water columns was found to be 0.133–0.203, lower than that in other marginal seas (e.g. the East/South China Seas and the Philippine Sea) of the western Pacific Ocean; this might be a result of the fast ventilation rate in this sea. The vertical Pb profile showed typical scavenged-type behavior with a surface maximum and deep minimum. From a comparison of inputs from the atmosphere and the Tsushima Warm Current, atmospheric deposition is substantial enough that it cannot be ignored, and its role in metal cycling is more significant in the offshore zone.     

Circulation patterns in the lower Arctic Ocean derived from geochemical data

Climatological water-mass structures were identified in the Arctic Ocean using the geochemical dataset in the Hydrochemical Atlas of the Arctic Ocean (HAAC) as well as data on a geochemically conserved parameter, PO₄*, based on phosphate and dissolved oxygen. In the upper ocean above a depth of 500 m, the HAAC was found to reliably depict the boundary between Pacific-Origin Water (P-Water) and Atlantic-Origin Water (A-Water), which is aligned 135°E–45°W near the surface but rotates counterclockwise with depth. Thus, the Arctic and Atlantic oceans exchange high-silicate P-Water and low-silicate A-Water. The PO₄* field in the lower ocean below a depth of 1500 m was analyzed statistically, and the results indicated that the Eurasian Basin receives low-PO₄* Nordic Seas Deep Water, which flows along the bottom from the Greenland Sea. The routes from the upper ocean to the lower ocean were determined. Only the southern portion of the Canada Basin, which receives water from the Chukchi and Beaufort Seas, has high PO₄* levels; the rest of the Amerasian Basin receives low-PO₄* water from the Laptev Sea and/or the Barents Sea. The Eurasian Basin receives moderate levels of PO₄* from the Fram Strait and from the intermediate layer. The intermediate-layer water gradually travels up from the lower ocean and returns to the Atlantic, entraining the subsurface portion. It is likely that high-PO₄* water occasionally flows down from the upper ocean along Greenland, making the Eurasian Basin heterogeneous.     

Variations in nutrients, carbon and other hydrographic parameters related to the 1976/77 and 1988/89 regime shifts in the sub-arctic Northeast Pacific

For time series at Station P (50°N, 145°W) and stations along Line P, long term changes in eight oceanographic and chemical parameters (sea surface temperature (SST), salinity, oxygen, phosphate (PO₄), silicate (SiO₄), nitrate (NO₃), dissolved inorganic carbon (DIC), and apparent oxygen utilisation (AOU)) were influenced by climate regime shifts with a “step change” of anomalies for nutrients and carbon in the sub-arctic Pacific during the 1976/77 and 1988/89 regime shifts. The presence of regime shifts in the data in the late 1970s and the late 1980s was supported by the statistical test of [Rodionov, S.N., 2004. A sequential algorithm for testing climate regime shifts. Geophysical Research Letters 31, L09204, doi:10.1029/2004GL019448], based on the Student t-test. The response of nutrients and carbon to the regime shifts was more intensive in 1976/77 than in 1988/89. Salinity, PO₄, SiO₄, NO₃, oxygen and DIC showed positive anomalies during 1950-1975 and negative ones during 1976-1995. The effect of La Niña on nutrients and carbon was larger than that of El Niño. Strong La Niña events (e.g. 1988/89) caused a sudden increase in nutrients and carbon. Two regime shifts (1976/77 and 1988/89) occurred just after two strong La Niña events in 1976/77 and 1988/89. At Station P, upwelling of nutrient-poor subsurface water tended to decrease the nutrients at the surface.     

Surface heat budget and heat balance in the oceanic mixed layer in the central equatorial Pacific ocean during the 1986–87 El Niño

In January–February 1987, an urgent cruise JENEX-87 was carried out in the central equatorial Pacific during the occurrence of the 1986–87 El Niño. This cruise, supported by the Japan Science and Technology Agency, supplied heat flux data through the sea surface, on the basis of direct measurements of short- and long-wave radiation fluxes.In the time average, the heat gain due to the radiation flux (153 W m^–2) was almost compensated by the heat loss due to latent heat flux (130 W m^–2), and thus the net heat gain was small in magnitude (20 W m^–2). On the other hand, day-to-day changes of the net heat flux ranged within ±130 W m^–2, mainly reflecting the downward short-wave radiation variations.The heat balance in the surface oceanic mixed layer was investigated in two quadrangle areas (160°E-180° and 180°-160°W between 2°N and 2°S), using the surface heat flux and estimating the advective heat fluxes due to the geostrophic and Ekman currents. In these two quadrangles, we respectively derived –187±88 W m^–2 and +27±95 W m^–2. The former value, which is equivalent to about 1°C month^–1 drop of the mixed layer temperature, is evidence of the abnormal oceanic condition in the occurrence of the 1986–87 El Niño event.     

Tidal time-scale variation in nutrient flux across the sediment–water interface of an estuarine tidal flat

We determined the range of the tidal variations in nutrient flux across the sediment–water interface and elucidated mechanisms of the flux variation in two estuarine intertidal flats (one sand, one mud) in northeastern Japan. Nutrient flux was measured using in situ light and dark chambers, which were incubated for 2 h, 2–6 times per day. Results showed that nutrient concentration in overlying water varied by tide and was also affected by sewage-treated water inflow. The nutrient fluxes responded quickly to the tidal variation in overlying water chemistry and the range of the variation in flux was as large as the seasonal-scale variation reported in previous studies. In the sand flat, salinity increase likely enhanced benthos respiration and led to increases in both O₂ consumption and PO₄³⁻ regeneration under low illumination, while benthic microalgae were likely to actively generate O₂, uptake PO₄³⁻ and suppress PO₄³⁻ release under high illumination (>900 μmol photons m⁻² s⁻¹). Also in the mud flat, PO₄³⁻ flux was related with O₂ flux, although the range of temporal variation in PO₄³⁻ flux was small. In both the flats, NH₄⁺ flux was always governed by NH₄⁺ concentration in the overlying water; either an increase in NH₄⁺ uptake or a decrease in NH₄⁺ release was observed as the NH₄⁺ concentration rose due to inflow of river water or input of sewage-treated water. Although NO₃⁻ tended to be released in both tidal flats when low NO₃⁻ concentration seawater dominated, their relationship was likely to be weakened under conditions of low oxygen consumption and suppressed denitrification. It is likely that tidal variation in nutrient flux is governed more by the nutrient concentration than other factors, such as benthic biological processes, particularly in the case where nutrient concentration in the overlying water is relatively high and with wide amplitude.     

Distribution of Trace Bioelements in the Subarctic North Pacific Ocean and the Bering Sea (the R/V Hakuho Maru Cruise KH-97-2)

A column concentration-high resolution inductively coupled plasma mass spectrometry (ICP-MS) determination was applied to measure the total dissolved concentrations of Fe, Co, Ni, Cu and Zn in seawater collected from the subarctic North Pacific (~45°N) and the Bering Sea in July–September 1997. Total adsorbable Mn was determined on board by column electrolysis preconcentration and chemiluminescence detection. The vertical profiles for Fe, Ni and Zn were nutrient-like. The deep water concentration of Fe was ~0.5 nM in the northeast Pacific (18°-140°W) and increased to ~1 nM in the northwest Pacific (161°E) and ~2 nM in the Bering Sea (57°N, 180°E). The deep water concentrations for Ni and Zn in the Bering Sea were also 1.3–2 times higher than in the North Pacific. The profiles for Co and Cu were examined in the subarctic North Pacific, and results obtained were consistent with previous reports. There was a significant correlation between the concentrations of Co and Mn except for surface mixed layer. The profiles for total adsorbable Mn were similar to the reported profiles for total dissolvable Mn. The deep water concentration of Mn in the Bering Sea was also 4 times higher than in the North Pacific. Iron and zinc were depleted in surface water of the subarctic North Pacific. The relationship between these trace elements and nutrients suggests that these elements could be a limiting factor of phytoplankton productivity. In the Bering Sea, surface water contained ~0.3 nM of Fe. The Zn concentration, which was less than the detection limit in surface water, increased at shallower depths (~30 m) compared with the subarctic North Pacific. These results imply a higher flux of Fe and Zn to surface water in the Bering Sea. This in turn may cause the ecosystem in the Bering Sea characterized by a dominance of diatoms and high regenerated production.