首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 249 毫秒
1.
Seventy percent of 342 seawater samples collected in the Bering Sea, North and South Pacific, Japan Sea, East and South China Seas, and Indian Ocean had concentrations of “total” mercury ranging from 3 to 6 ng Hg l?1 with an arithmetic mean of 5.3 ng l?1 and a geometric mean of 5.0 ng l?1. In some cases, a higher concentration was observed at the surface, at the halocline or thermocline, or in the bottom water. But in general, there was no consistent correlation between mercury concentration and depth, except for a statistical tendency for mercury concentration to be slightly higher in the surface water. This tendency suggests that mercury in the ocean is supplied from the atmosphere by rain washout. The latitudinal variation of surface mercury concentrations showed that the maximum concentration at each latitude decreased from 40°N to 30°S. This variation provides evidence that atmospheric mercury is emitted mainly from continental areas naturally or anthropogenically.  相似文献   

2.
Marine aerosol samples collected from the North Pacific atmosphere were studied for molecular distributions of dicarboxylic acids by using a capillary gas chromatography and mass spectrometery. A homologous series of dicarboxylic acids (C2–C10) was detected in the marine aerosol samples as dibutyl esters. All the samples showed that the smallest diacid (oxalic acid: C2) was the most abundant and comprised 41–67% of the total diacids. The second most abundant species was malonic acid (C3) or succinic acid (C4). The diacids with more carbon numbers were generally less abundant. Total diacid concentration range was 17–1040 ng m–3, which accounted for up to 1.6% of total aerosol mass. This indicates that low molecular weight dicarboxylic acids are important class of organic compounds in the marine atmosphere. The concentrations were generally higher in the western North Pacific and lower in the central North Pacific. The major portion of diacids is probably derived from the Asian Continent and East Asian countries by long-range atmospheric transport and partly fromin situ photochemical production in the marine atmosphere.  相似文献   

3.
Horizontal and vertical distributions of mercury were determined in seawater in Minamata Bay and Yatsushiro Sea. The concentrations of total and particulate mercury respectively ranged from 56–285 ng l–1 and 2.1–506 ng l–1. They were both highest in the inner most part of Minamata Bay where the sediment was most heavily polluted, and decreased with increasing distance from there. Vertically, an evident increase in concentration was observed near the bottom. A good agreement was found between the mercury content in suspended matter and that in fine sediment particles.These facts show that the particulate mercury is supplied mostly from the bottom sediment, and that it is spreading offshore with dispersing in seawater. This process would eventually result in the pollution of sediment in Yatsushiro Sea.  相似文献   

4.
Determination of the actual mercury concentration in Mediterranean basin seawater was achieved by means of an instrument based on fluorescence spectrometry developed for this purpose, during a field study aboard the oceanographic ship “L.F. Marsili”, between August 1980 and May 1982.Dissolved ·total’ and ·reactive’ mercury and mercury associated with particulate matter were determined on surface and subsurface waters in the Tyrrhenian Sea from La Spezia to Sicily.Concentrations in the range 1.4–19.7 ng l−1 for ·total dissolved mercury’, 0.5–5.9 ng l−1 for ·reactive dissolved mercury’ and 0.3–8.0 ng l−1 for mercury associated with the particulate matter, were measured on surface and subsurface waters in the Tyrrhenian Sea from La Spezia to Sicily.Even if the mean value of the total mercury concentration (dissolved + particulate) was found to be about twice as high as those observed for the oceans, the difference does not seem to be as high as predicted by the model proposed by Buffoni and co-workers to explain the large difference of mercury levels between tunas caught, respectively, in the Mediterranean and in the Oceans.  相似文献   

5.
Measurements of zinc and zinc complexation by natural organic ligands in the northeastern part of the Atlantic Ocean were made using cathodic stripping voltammetry with ligand competition. Total zinc concentrations ranged from 0.3 nM in surface waters to 2 nM at 2000 m for open-ocean waters, whilst nearer the English coast, zinc concentrations reached 1.5 nM in the upper water column. In open-ocean waters zinc speciation was dominated by complexation to a natural organic ligand with conditional stability constant (log KZnL′) ranging between 10.0 and 10.5 and with ligand concentrations ranging between 0.4 and 2.5 nM. The ligand was found to be uniformly distributed throughout the water column even though zinc concentrations increased with depth. Organic ligand concentrations measured in this study are similar to those published for the North Pacific. However the log KZnL′ values for the North Atlantic are almost and order of magnitude lower than those reported by Bruland [Bruland, K.W., 1989. Complexation of zinc by natural organic-ligands in the central North Pacific. Limnol. Oceanogr., 34, 269–285.] using anodic stripping voltammetry for the North Pacific. Free zinc ion concentrations were low in open-ocean waters (6–20 pM) but are not low enough to limit growth of a typical oceanic species of phytoplankton.  相似文献   

6.
Concentrations of total carbonate, alkalinity and dissolved oxygen were obtained near the 1973 GEOSECS stations in the North Pacific subpolar region north of 40°N along 175°E between 1993 and 1994. A difference of excess CO2 content between the GEOSECS and our expeditions was estimated. The maximum difference in water column inventory of excess CO2 has increased by about 280 gC m–2 above 2000 m depth which apparently means an uptake of excess CO2 taken from air to sea during the last two decades. An averaged value of the annual flux of excess CO2 at 75–1000 m depth was 8.63±2.01 gC m–2yr–1 in the North Pacific subpolar region. By introducing the annual flux of excess CO2 into a two-box model for the North Pacific subpolar region, a penetration factor of excess CO2 from air to sea was obtained to be 1.08×10–2 gC m–3ppm–1 in the North Pacific subpolar region. Based on this factor, the surface concentration of excess CO2 in the North Pacific subpolar region was estimated to be 68 mole I–1, suggesting that the North Pacific subpolar region absorbed atmospheric excess CO2 more than the saturated concentration of excess CO2. Total amount of excess CO2 taken from the North Pacific subpolar region by 1993 was estimated to be 36.2×1015 gC, which was equal to about one tenth of that released by human activities after the preindustrial era.  相似文献   

7.
Dissolved and particulate concentrations of the biogenic thiols cysteine (Cys), arginine–cysteine (Arg–Cys), glutamine–cysteine (Gln–Cys), γ-glutamate–cysteine (γ-Glu–Cys) and glutathione (GSH) were measured in the subartic Pacific Ocean in the summer of 2003 using high performance liquid chromatography (HPLC) with precolumn derivatization as reported in previous work. In this study, a preconcentration protocol for the derivatized thiols was utilized to extend detection limits of dissolved thiols to picomolar levels. The measured concentrations of particulate and dissolved thiols were uncoupled, with distinctive depth profiles and large differences in the particulate to dissolved ratios between individual compounds. Glutathione was the most abundant particulate thiol whereas the most abundant dissolved thiol was γ-Glu–Cys, with concentrations as high as 15 nM. Given the relatively small pool of intracellular γ-Glu–Cys and the very low dissolved concentrations of GSH, we hypothesize that glutathione released from cells is rapidly converted to the potentially degradation resistant γ-Glu–Cys outside the cell. The relatively high concentrations of other dissolved thiols compared to particulate concentrations implies both biological exudation and slow degradation rates. Some thiols appear to vary with changes in nutrient availability but this effect is difficult to decouple from changes in community structure inferred from pigment analyses. Dissolved thiol concentrations also exceed typical metal concentrations in the subartic Pacific, supporting previous arguments that they may be important in metal speciation.  相似文献   

8.
Hydrographic measurements by CTD were made in the western-central Equatorial Pacific (160°W–147°E) during the Japanese Pacific Climate Study cruise in January–February 1991. InT-S diagram, three water masses are seen in the layer of kg/m3: salinity water corresponding to the Tropical Water of eastern South Pacific origin, less saline water in the North Pacific, and water with salinity between the above two, found on the equator. In three meridional sections (160°W–160°E), the Tropical Water of eastern South Pacific origin extends further equatorward than the climatological data of Levitus (1982).  相似文献   

9.
The Mussel Watch program conducted along the French coasts for the last 20 years indicates that the highest mercury concentrations in the soft tissue of the blue mussel (Mytilus edulis) occur in animals from the eastern part of Seine Bay on the south coast of the English Channel, the “Pays de Caux”. This region is characterized by the presence of intertidal and submarine groundwater discharges, and no particular mercury effluent has been reported in its vicinity. Two groundwater emergence systems in the karstic coastal zone of the Pays de Caux (Etretat and Yport with slow and fast water percolation pathways respectively) were seasonally sampled to study mercury distribution, partitioning and speciation in water. Samples were also collected in the freshwater–seawater mixing zones in order to compare mercury concentrations and speciation between these “subterranean” or “groundwater” estuaries and the adjacent macrotidal Seine estuary, characterized by a high turbidity zone (HTZ). The mercury concentrations in the soft tissue of mussels from the same areas were monitored at the same time.The means of the “dissolved” (< 0.45 μm) mercury concentrations (HgTD) in the groundwater springs were 0.99 ± 0.15 ng l− 1 (n = 18) and 0.44 ± 0.17 ng l− 1 (n = 17) at Etretat and Yport respectively. High HgTD concentrations were associated with strong runoff over short water pathways during storm periods, while low concentrations were associated with long groundwater pathways. Mean particulate mercury concentrations were 0.22 ± 0.05 ng mg− 1 (n = 16) and 0.16 ± 0.10 ng mg− 1 (n = 17) at Etretat and Yport respectively, and decreased with increasing particle concentration probably as a result of dilution by particles from soil erosion. Groundwater mercury speciation was characterized by high reactive-to-total mercury ratios in the dissolved phase (HgRD/HgTD: 44–95%), and very low total monomethylmercury concentrations (MMHg < 8 pg l− 1). The HgTD distributions in the Yport and Etretat mixing zones were similar (overall mean concentration of 0.73 ± 0.21 ng l− 1, n = 43), but higher than those measured in the adjacent industrialized Seine estuary (mean: 0.31 ± 0.11 ng l− 1, n = 67). In the coastal waters along the Pays de Caux dissolved monomethylmercury (MMHgD) concentrations varied from 9.5 to 13.5 pg l− 1 (2 to 8% of the HgTD). Comparable levels were measured in the Seine estuary (range: 12.2– 21.1 pg l−1; 6–12% of the HgTD). These groundwater karstic estuaries seem to be mostly characterized by the higher HgTD and HgRD concentrations than in the adjacent HTZ Seine estuary. While the HTZ of the Seine estuary acts as a dissolved mercury removal system, the low turbid mixing zone of the Pays de Caux receives the dissolved mercury inputs from the groundwater seepage with an apparent Hg transfer from the particulate phase to the “dissolved” phase (< 0.45 μm). In parallel, the soft tissue of mussels collected near the groundwater discharges, at Etretat and Yport, exhibited significantly higher values than those found in the mussel from the mouth of the Seine estuary. We observe that this difference mimics the differences found in the mercury distribution in the water, and argue that the dissolved phase of the groundwater estuaries and coastal particles are significant sources of bioavailable mercury for mussels.  相似文献   

10.
Occurrence of the depth differences in pigment composition and photosynthetic properties of marine phytoplankton were examined in relation to the spectral changes of light with depth. Phytoplankton were taken from various depths in the northwestern North Pacific, and their absorption spectra were determined with intact cells and in 90% acetone extract. The photosynthetic activities of phytoplankton were concurrently measured under blue, green, red and white light. The difference in absorption spectra for the surface and deeper samples was considerably small, indicating that the prevailing green or blue light in the deeper layers may have little significance for depth-variations of the pigment composition in marine phytoplankton. The depth differentiation in the shape of the light-photosynthesis curve was marked in a well stratified water column but no active response of deeper phytoplankton to green light could be confirmed. The photosynthetic efficiencies of phytoplankton for blue and green light were approximately 105–115 % and 80–90 % of white light, respectively, irrespective of sampling depth.Contribution No. 261 from Shimoda Marine Biological Station  相似文献   

11.
Autotrophic and microheterotrophic plankton populations were monitored in the euphotic zone of the eastern subarctic Pacific during 6 one-month cruises in spring and summer, 1984, 1987 and 1988. Transmitted light, epifluorescence, and electron microscopy were used to identify, enumerate and estimate the biomass of size-populations of species. The 2–10μm size class dominated the biomass of both autotrophs and heterotrophs. The autotrophic flagellate, Phaeocystis pouchetii, was frequently observed in its non-colonial phase. Temporal variation in all the stocks was evident and could be explained only partially by the physical, chemical or biological factors investigated here. The general structure of the autotrophic community was similar to that in the North Atlantic, but major, unexplained variations between cruises occurred. Variation in mixed-layer depth and day length (but not variation in daily insolation) explained 25% of the variation in autotrophic doubling rate. Heterotrophic biomass comprised, in decreasing order of importance, non-pigmented flagellates, dinoflagellates, and ciliates. Ciliates rarely contributed more than 40% to the total. Microheterotrophic biomass rarely exceeded 30μg C 1−1 (avg 15μg C 1−1, 0–60m) whereas autotrophic biomass averaged 20μg C 1−1, 0–60m, and reached 74μg C 1−1 on one occasion, yet the grazing capacity of these microheterotrophs averaged 100% of primary production.  相似文献   

12.
We found high potential activities of alkaline phosphatase associated with particles (0.2 μm or greater size fraction) in deep waters (1000–4000 m) of the central Pacific Ocean. The potential enzyme activity at depth (0.03 – 0.3 nM h−1) was up to 50% of that at the surface (0–125 m). In contrast, activities of α- and β-d-glucosidase in the deep layer were low (generally less than 1 % of those in the upper layer), yielding up to two orders of magnitude difference in the ratio of alkaline phosphatase and α- and β-d-glucosidase activities with depth. It is unlikely that the phosphatase is actively produced by microorganisms inhabiting the deep-sea environment, where labile organic carbon supply is limited and phosphate concentration is high (2.4 – 3.0 AM). Instead, deep-water phosphatase is probably supplied by rapidly sinking particles and their subsequent fragmentation and dissolution. Different distributions of phosphatase and glucosidase indicate that sinking particles of phytoplankton origin are an important source of alkaline phosphatase enzymes in the deep sea.  相似文献   

13.
Diel changes in vertical distribution and feeding conditions of the chaetognath Parasagitta elegans (Verill) were observed in three regions of the subarctic North Pacific in the summer of 1997. Samples were collected by repeated vertical hauls with a Vertical Multiple Plankton Sampler (VMPS) for 15–45 hours by demarcating the 0–500 m water column into four sampling layers. Integrated abundance through the entire water column and the proportion of juveniles were higher in the Bering Sea than the western and eastern subarctic Pacific. Juveniles always inhabited the surface layer in the western subarctic Pacific and Bering Sea, but they inhabited the underlying layer in the eastern subarctic Pacific. Stages I–III concentrated into the upper 150 m in the western subarctic Pacific but were distributed widely from 20–300 m in the Bering Sea. Among them, Stages II and III migrated rather synchronously over a wide vertical range in the eastern subarctic Pacific. The feeding rate of P. elegans was calculated to be 0.18 prey/chaetognath/day in the western subarctic Pacific, 0.27 prey/chaetognath/day in the Bering Sea and 0.07 prey/chaetognath/day in the eastern subarctic Pacific.  相似文献   

14.
The whole core squeezing method was used to simultaneously obtain profiles of nitrous oxide (N2O), nitrogenous nutrients, and dissolved oxygen in sediments of Koaziro Bay, Japan (coastal water), the East China Sea (marginal sea), and the central Pacific Ocean (open ocean). In the spring of Koaziro Bay, subsurface peaks of interstitial N2O (0.5–3.5 cm depth) were observed, at which concentrations were higher than in the overlying water. This was also true for nitrate (NO3−) and nitrite (NO2−) profiles, suggesting that the transport of oxic overlying water to the depth through faunal burrows induced in situ N2O production depending on nitrification. In the summer of Koaziro Bay, sediment concentrations of N2O, NO3− and NO2− were lower than in the overlying water. In most East China Sea sediments, both N2O and NO3− decreased sharply in the top 0.5–2 cm oxic layer (oxygen: 15–130 μM), which may have indicated N2O and NO3− consumption by denitrification at anoxic microsites. N2O peaks at subsurface depth (0.5–6.5 cm) implied in situ production of N2O and/or its supply from the overlying water through faunal burrows. However, the occurrence of the latter process was not confirmed by the profiles of other constituents. In the central Pacific Ocean, the accumulation of N2O and NO3− in the sediments likely resulted from nitrification. Nitrous oxide fluxes from the sediments, calculated using its gradient at the sediment–water interface and the molecular diffusion coefficient, were −45 to 6.9 nmolN m−2 h−1 in Koaziro Bay in the spring, −29 to −21 nmolN m−2 h−1 in the summer, −46 to 37 nmolN m−2 h−1 in the East China Sea, 0.17 to 0.23 nmolN m−2 h−1 in the equatorial Pacific, and <±0.2 nmolN m−2 h−1 in the subtropical North Pacific, respectively.  相似文献   

15.
Sediments and organisms were examined for concentrations of organic and metal contaminants from near the Los Angeles County (JWPCP) municipal outfall at Palos Verdes (PV) station 7-3, the Los Angeles City (Hyperion) municipal outfall at Santa Monica Bay (SMB) station 6-4 and reference station SMB 2–3 near Malibu Beach. Flows and mass emission rates of suspended solids, PCBs, Cd and Zn were similar at the two outfalls. Mass emission rate of copper was almost twice as high from Hyperion as from JWPCP, while mass emission rate of DDTs was an order or magnitude higher from JWPCP than from Hyperion.Surficial sediments at PV 7-3 were enriched in most contaminants relative to SMB 6-4 and relative to the mass emission rates of contaminants from the JGVPCP and Hyperion outfalls. Some of this enrichment could be accounted for by the greater accumulation of organic material, measured as total volatile solids, at PV 7-3 relative to SMB 6-4. Some might be accounted for by resurfacing of more contaminated historical deposits buried at PV 7-3. Some of the enrichment of DDTs relative to PCBs could be accounted for by the greater abundance of oxygenated metabolites of PCBs (PCBols) relative to DDTs (DDTols) in sediments.The degree of contamination of organisms by DDTs increased with proximity to PV 7-3 but contamination by PCBs was similar at PV 7-3 and SMB 6-4. DDT concentrations in fish livers ranged from 12 ± 4 ( ) mg/wet kg in longspine combfish from SMB 2–3 to 610 ± 105 (n = 5) mg/wet kg in Pacific sanddab from PV 7-3. DDT concentrations in fish gonads ranged from 0·003 ± 0·003 (n = 5) mg/wet kg in yellowchin sculpin from SMB 6-4 to 1.5 ± 6 (n = 3) mg/wet kg in Pacific sanddabs from PV 7-3. PCB concentrations in fish livers ranged from 1·2 ± 0·4 (n = 4) mg/wet kg in yellowchin sculpin from SMB 2–3 to 16 ± 3 (n = 6) in Pacific Sanddab from SMB 6-4. DDT and PCB concentrations in invertebrate hepatopancreas were only slightly lower than those in fish livers. DDTols and PCBoIs comprised an average of 91 % of the total of parent compounds and oxygenated metabolites in sediments and 66 % in livers and hepatopancreas. Trace metals were frequently decreased in livers and hepatopancreas from near outfalls even though they were highly elevated in sediments.Comparison of sediment and tissue chlorinated hydrocarbon data with that from Elliot and Commencement Bays, Puget Sound, indicated that none of the southern California coastal stations considered in this study were sufficiently lacking contamination to be considered as adequate control sites.  相似文献   

16.
Two-dimensional temperature data observed by use of a 275 meter towed thermistor chain deployed from an oceanographic research vessel USS MARYSVILLE, which cruised with a speed of 6.2 knots in July 1966 across the Kuroshio Extension in the North Pacific, are investigated. Two-dimensional variations of the distribution of the isotherms along the ship's track are analyzed with special reference to their slope, wavelength and wave height. The results show that the slope and wave height of isotherms have a tendency to increase as the temperature decreases. Even if the contribution of wave heights smaller than 1.5 m is neglected, i.e., contribution of large scale slope with a horizontal scale of 5–30 km is subtracted, this tendency is still detected. In contrast to this, the wavelength evaluated by the crest to crest method has no dependency on the temperature. Power spectrum of the isotherm depth is proportional tok –1.87 for 13°C andk –2.13 for 27°C, wherek is the wave number. It is shown that the spectra of warmer isotherms are relatively well approximated by –2 power law (Garrett and Munk spectrum) for internal waves rather than the –5/3 power law (Kolmogorov spectrum) for three dimensional isotropic turbulence.  相似文献   

17.
Oxygen minimum zones in the eastern tropical Atlantic and Pacific oceans   总被引：2，自引：0，他引：2  
Within the eastern tropical oceans of the Atlantic and Pacific basin vast oxygen minimum zones (OMZ) exist in the depth range between 100 and 900 m. Minimum oxygen values are reached at 300–500 m depth which in the eastern Pacific become suboxic (dissolved oxygen content <4.5 μmol kg−1) with dissolved oxygen concentration of less than 1 μmol kg−1. The OMZ of the eastern Atlantic is not suboxic and has relatively high oxygen minimum values of about 17 μmol kg−1 in the South Atlantic and more than 40 μmol kg−1 in the North Atlantic. About 20 (40%) of the North Pacific volume is occupied by an OMZ when using 45 μmol kg−1 (or 90 μmol kg−1, respectively) as an upper bound for OMZ oxygen concentration for ocean densities lighter than σθ < 27.2 kg m−3. The relative volumes reduce to less than half for the South Pacific (7% and 13%, respectively). The abundance of OMZs are considerably smaller (1% and 7%) for the South Atlantic and only 0% and 5% for the North Atlantic. Thermal domes characterized by upward displacements of isotherms located in the northeastern Pacific and Atlantic and in the southeastern Atlantic are co-located with the centres of the OMZs. They seem not to be directly involved in the generation of the OMZs.OMZs are a consequence of a combination of weak ocean ventilation, which supplies oxygen, and respiration, which consumes oxygen. Oxygen consumption can be approximated by the apparent oxygen utilization (AOU). However, AOU scaled with an appropriate consumption rate (aOUR) gives a time, the oxygen age. Here we derive oxygen ages using climatological AOU data and an empirical estimate of aOUR. Averaging oxygen ages for main thermocline isopycnals of the Atlantic and Pacific Ocean exhibit an exponential increase with density without an obvious signature of the OMZs. Oxygen supply originates from a surface outcrop area and can also be approximated by the turn-over time, the ratio of ocean volume to ventilating flux. The turn-over time corresponds well to the average oxygen ages for the well ventilated waters. However, in the density ranges of the suboxic OMZs the turn-over time substantially increases. This indicates that reduced ventilation in the outcrop is directly related to the existence of suboxic OMZs, but they are not obviously related to enhanced consumption indicated by the oxygen ages. The turn-over time suggests that the lower thermocline of the North Atlantic would be suboxic but at present this is compensated by the import of water from the well ventilated South Atlantic. The turn-over time approach itself is independent of details of ocean transport pathways. Instead the geographical location of the OMZ is to first order determined by: (i) the patterns of upwelling, either through Ekman or equatorial divergence, (ii) the regions of general sluggish horizontal transport at the eastern boundaries, and (iii) to a lesser extent to regions with high productivity as indicated through ocean colour data.  相似文献   

18.
Water samples were collected monthly for 3 years at 66°N, 2°E in the Norwegian Sea, 250 nautical miles off the Norwegian coast. Concentrations of mono- and polysaccharides were measured with the 2,4,6-tripyridyl-s-triazine (TPTZ) spectroscopic method. Total dissolved carbohydrates varied from 3.4 to 28.2 μM C of all samples and the ratio of carbohydrate to dissolved organic C (DOC) varied from an average of 14% at 0–25 m depth to 11% at 800–2000 m depth. This indicates that dissolved carbohydrates were a significant constituent of DOC in the Norwegian Sea. Polysaccharides varied from 0.4 to 21.5 μM C and monosaccharides from 0.7 to 11.7 μM C at all depths. The level of monosaccharides was relatively constant at 2.8–3.2 μM C below the euphotic zone, whereas polysaccharides showed more varying concentrations. Dissolved carbohydrates accumulated during the productive season, reaching maximum concentrations during summer although interannual differences were observed. A significant positive correlation between Chl a and soluble carbohydrate was found in one growing season with nutrient analyses. Average values for total carbohydrates were highest in the surface – 0 to 25 m – with 13.3 μM C and decreased to 8.4 μM C at 800–2000 m depth. The ratio of monosaccharides to polysaccharides exhibited a marked seasonal variation, increased from January to a maximum in June of 1.1, and declined to 0.5 in July.  相似文献   

19.
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.  相似文献   

20.
We proposed an empirical equation of sea surface dimethylsulfide (DMS, nM) using sea surface temperature (SST, K), sea surface nitrate (SSN, μM) and latitude (L, °N) to reconstruct the sea surface flux of DMS over the North Pacific between 25°N and 55°N: ln DMS = 0.06346 · SST − 0.1210 · SSN − 14.11 · cos(L) − 6.278 (R2 = 0.63, p < 0.0001). Applying our algorithm to climatological hydrographic data in the North Pacific, we reconstructed the climatological distributions of DMS and its flux between 25 °N and 55 °N. DMS generally increased eastward and northward, and DMS in the northeastern region became to 2–5 times as large as that in the southwestern region. DMS in the later half of the year was 2–4 times as large as that in the first half of the year. Moreover, applying our algorithm to hydrographic time series datasets in the western North Pacific from 1971 to 2000, we found that DMS in the last three decades has shown linear increasing trends of 0.03 ± 0.01 nM year− 1 in the subpolar region, and 0.01 ± 0.001 nM year− 1 in the subtropical region, indicating that the annual flux of DMS from sea to air has increased by 1.9–4.8 μmol m− 2 year− 1. The linear increase was consistent with the annual rate of increase of 1% of the climatological averaged flux in the western North Pacific in the last three decades.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号