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1.
Recent carbonate data collected in the North Pacific were combined with the data in the literature in order to understand more clearly the carbonate chemistry in the North Pacific. Our analyses show that inorganic CaCO3 dissolution contributes about 26% of the total inorganic CO2 increase of deep water, after leaving the Southern Ocean. The calcium and alkalinity data indicate a CaCO3 dissolution rate of 0.060±0.010 and 0.053±0.005 µ mol kg–1 yr–1 respectively, for waters deeper than 2,000 m in reference to the Weddell Sea Deep Water. The organic carbon decomposition rate is 0.107±0.012 µ mol kg–1 yr–1 while the oxygen consumption rate is 0.13±0.002 µ mol kg–1 yr–1. These results which are based on the direct comparison of two water masses agree well with other estimates which are based on methods such as the one-dimensional-diffusion-advection model. Comparison of data along the two sections at 165°E and 150°W shows no significant difference in the ratio of the CaCO3 dissolution rate and the organic carbon decomposition rate. The eastern section, however, has a higher TCO2 input than the western section because of the older age of the deep water along the eastern section.  相似文献   

2.
The accumulation rates of sediment cores in Osaka Bay have been determined by using210Pb dating technique. In the upper 10 cm210Pbex contents show a constant value with depth. The accumulation rates below the homogeneous layer of sediments ranging from 0.12 to 0.61cm y–1 (0.067–0.34 g cm–2 y–1) were obtained. The higher contents of Zn, Cu, Pb and Cr were observed in the upper 10 to 30 cm of sediments. Assuming that the increment of heavy metal content in sediments is due to anthropogenic origin, the amount of anthropogenic input of heavy metals into sediments were estimated to be 1,300–2,700g cm–2 for Zn, 150 – 480 for Cu, 360 – 410 for Pb and 320 – 480 for Cr. The increment appears to start about 100 years ago. In surfical sediments most of heavy metal contents exceeded the background content, and then most part of Osaka Bay is polluted by heavy metals.  相似文献   

3.
Concentrations and inventories of137Cs and239,240Pu were determined in sea waters and sediments columns from the western North Pacific from 1980 to 1986.The239,240Pu/137Cs activity ratio in the water column shows a tendency to increase from the surface (10–3) to bottom waters (10–1), but the ratio in sediment is within a rather narrow range (10–2 to 10–1), indicating more effective removal of plutonium from the water column than137Cs. In regions south of 40N, the radionuclide inventories in the water column significantly exceed the estimated global fallout (stratospheric fallout due to the atmospheric nuclear explosion), especially in the case of239,240Pu. These excess inventories imply that local or close-in fallout derived from nuclear explosions in the equatorial North Pacific are well-preserved and retained in the regions, despite about 20 years since the atmospheric nuclear explosion moratorium. Data suggesting lateral transport of137Cs in surface water from north of 40N to southern regions is shown. Some data on90Sr contents are also shown.  相似文献   

4.
Sedimentation rates were determined with the210Pb technique in six sediment cores from Harima Nada (Harima Sound), Seto Inland Sea. The rate of deposition varies from 0.11 g cm–2y–1 in the northern part to 0.33 g cm–2 y–1 in the southern part of the basin. A marked increase in copper and zinc content was observed above a depth in the core corresponding to about 1900 A.D. as a result of increasing human activities. Anthropogenic input of copper and zinc decreased slightly after 1970. Natural background levels of copper and zinc in the sediment in this sound are 11–16 ppm and 100–120 ppm, respectively. The total amounts of anthropogenic copper and zinc in the sediments were estimated to be 110–180g cm–2 and 610–1,280g cm–2, respectively. These values constitute 40–50% of the total sedimentary input of copper and zinc in the sediments since about 1900 A.D.  相似文献   

5.
The metal load into sediments and the change in the sedimentary environment of Osaka Bay in the Seto Inland Sea have been studied through geochemical analysis of core sediments, using both Pb-210 dating and a selective chemical leaching technique. Analytical results from a 6-m core of sediment show that copper and zinc pollution started in the late 1800's and the present enrichment ratios of copper and zinc, relative to background levels (20 mg kg–1 for Cu and 94 mg kg–1 for Zn), are 2.8 and 4.1, respectively. The present anthropogenic copper and zinc loads into Osaka Bay sediments, are 47 and 368 ton yr–1, while natural copper and zinc loads are 40 and 186 ton yr–1, respectively. Osaka Bay sediment at the present day is considered to be seriously polluted by zinc, now. The vertical profiles of copper and zinc in four successively separated fractions (10% acetic acid soluble fraction: F-HAC, 0.1M hydrochloric acid-soluble fraction: F-HCl, hydrogen peroxide-soluble fraction: F-H2O2 and hydrofluoric acid-soluble fraction: F-HF) from the core sediments indicate that enrichments of copper and zinc in the upper layer of the sediment are dependent on increases in the metal contents of the F-HAC, F-HCl and F-H2O2 fractions. Copper in F-HAC, and zinc in F-HAC and F-HCl, seem to be of anthropogenic origin.Results of sequential studies of the whole Seto Inland Sea can be summarized as follows: At the present time, the sedimentary loads of copper and zinc over the whole Seto Inland Sea area are 630 and 3,500 ton yr–1, respectively, while the natural and anthropogenic loads are 320 and 310 ton yr–1 for copper and 1,800 and 1,700 ton yr–1 for zinc, respectively.  相似文献   

6.
Rivers draining into the Gulf of Papua (GOP) from the Papua New Guinea mainland deliver approximately 340 × 106 t yr–1 of sediment to the marine environment. The terrestrially derived sediment contains 1.1 ± 0.2% particulate organic carbon with a carbon-isotope composition of –26.5 ± 0.2, and amounts to 3.7 ± 0.7 × 106 t yr–1. The carbon-isotope composition of sediments in the Gulf of Papua indicates that 40% of the sediment cover contains 75% or more terrestrially derived carbon. Suspended sediments that are transported beyond the delta complex of the Fly River are transported north and northwest, augmented by sediments from other rivers along the coast of the GOP. The carbon-isotope results suggest that a significant quantity of terrestrially derived sediment escapes from the GOP, either along the coastlines to east and west or into the deep ocean via the Moresby and Pandora troughs. Little sediment travels south onto the Great Barrier Reef shelf. Extrapolating the results from this study to the region of Oceania suggests a total flux of particulate organic carbon to the world's oceans from the islands of Oceania of ~ 90 × 106 t yr–1 or twice the flux of riverine POC from the major rivers of North America, South America, and Africa combined. While such a calculation must be considered illustrative only, the similar tectonic, geomorphologic, and climatic features of the islands of Oceania suggest that the calculation is unlikely to be grossly in error and that the rivers of Oceania therefore represent a major but poorly documented source of sediment and organic carbon to the global ocean.  相似文献   

7.
Rates of sediment accumulation and microbial mineralization were examined at three Kandelia candel forests spanning the intertidal zone along the south coastline of the heavily urbanized Jiulongljiang Estuary, Fujian Province, China. Mass sediment accumulation rates were rapid (range: 10–62 kg m−2 y−1) but decreased from the low- to the high-intertidal zone. High levels of radionuclides suggest that these sediments originate from erosion of agricultural soils within the catchment. Mineralization of sediment carbon and nitrogen was correspondingly rapid, with total rate of mineralization ranging from 135 to 191 mol C m−2 y−1 and 9 to 11 mol N m−2 y−1; rates were faster in summer than in autumn/winter. Rates of mineralization efficiency (70–93% for C; 69–92% for N) increased, as burial efficiency (7–30% for C; 8–31% for N) decreased, from the low-to the high-intertidal mangroves. Sulphate reduction was the dominant metabolic pathway to a depth of 1 m, with rates (19–281 mmol S m−2 d−1) exceeding those measured in other intertidal deposits. There is some evidence that Fe and Mn reduction-oxidation cycles are coupled to the activities of live roots within the 0–40 cm depth horizon. Oxic respiration accounted for 5–12% of total carbon mineralization. Methane flux was slow and highly variable when detectable (range: 5–66 μmol CH4 m−2 d−1). Nitrous oxide flux was also highly variable, but within the range (1.6–106.5 μmol N2O m−2 d−1) measured in other intertidal sediments. Rates of denitrification were rapid, ranging from 1106 to 3780 μmol N2 m−2 d−1, and equating to 11–20% of total sediment nitrogen inputs. Denitrification was supported by rapid NH4 release within surface deposits (range: 3.6–6.1 mmol m−2 d−1). Our results support the notion that mangrove forests are net accumulation sites for sediment and associated elements within estuaries, especially Kandelia candel forests receiving significant inputs as a direct result of intense human activity along the south China coast.  相似文献   

8.
Momentum and heat flux were measured with a sonic anemometer at the Marine Observation Tower in the port of ItÔ. Under unstable conditions (T w -T a =3C4C), using the eddy correlation method, results show thatCd=(1.2±0.3)×10–3 andCh=(1.5±0.3)×10–3 at 5.5 m above mean sea level except for the case of weak winds.An unexpected relationship betweenCd and (–z/L) was observed, that is,Cd decreases as (–z/L) increases. If roughness variation over the sea is taken into account, we can explain the decrease in the range of (–z/L) less than 1, but not in the range greater than 1. This is due to a strong instability effect and the change of roughness class, from moderately rough to smooth.  相似文献   

9.
Marked fluctuation of concentrations of90Sr and137Cs was observed in the bottom waters at the entrance of Wakasa Bay during 1987–1992, and the cause was investigated. The concentrations of90Sr and137Cs in the bottom waters were significantly low when the upper level of the Japan Sea Proper Water (JSPW) was high and covered the sampling depth, but high when the upper level of the JSPW was low. The cause of the fluctuation observed in the bottom waters is, therefore, suggested to be the vertical fluctuation of the upper level of the JSPW on the shelf slope, which has been little described before.  相似文献   

10.
A systematic investigation of fluxes and compositions of lipids through the water column and into sediments was conducted along the U.S. JGOFS EgPac transect from l2°N to l5°S at 140°W. Fluxes of lipids out of the euphotic zone varied spatially and temporally, ranging from ≈0.20 – 0.6 mmol lipid-C m−2 day−1. Lipid fluxes were greatly attenuated with increasing water column depth, dropping to 0.002-0.06 mmol lipid-C m−2 day−1 in deep-water sediment traps. Sediment accumulation rates for lipids were ≈ 0.0002 – 0.00003 mmol lipid-C m−2 day−1. Lipids comprised ≈ 11–23% of Corg in net-plankton, 10–30% in particles exiting the euphotic zone, 2–4% particles in the deep EgPac, and 0.1-1 % in sediments. Lipids were, in general, selectively lost due to their greater reactivity relative to bulk organic matter toward biogeochemical degradation in the water column and sediment. Qualitative changes in lipid compositions through the water column and into sediments are consistent with the reactive nature of lipids. Fatty acids were the most labile compounds, with polyunsaturated fatty acids (PUFAs) being quickly lost from particles. Branchedchain C15 and C17 fatty acids increased in relative abundance as particulate matter sank and was incorporated into the sediment, indicating inputs of organic matter from bacteria. Long-chain C39 alkenones of marine origin and long-chain C20-C30 fatty acids, alcohols and hydrocarbons derived from land plants were selectively preserved in sediments. Compositional changes over time and space demonstrate the dynamic range of reactivities among individual biomarker compounds, and hence of organic matter as a whole. A thorough understanding of biogeochemical reprocessing of organic matter in the oceanic water column and sediments is, thus, essential for using the sediment record for reconstructing past oceanic environments.  相似文献   

11.
Sedimentation rates were determined for the northern Gulf of Mexico margin sediments at water depths ranging from 770 to 3560 m, using radiocarbon determinations of organic matter. Resulting sedimentation rates ranged from 3 to 15 cm/kyr, decreasing with increasing water depth. These rates agree with long-term sedimentation rates estimated previously using stratigraphic methods, and with estimates of sediment delivery rates by the Mississippi River to the northern Gulf of Mexico, but are generally higher by 1–2 orders of magnitude than those estimated by 210Pbxs methods. Near-surface slope sediments from 2737 m water depth in the Mississippi River fan were much older than the rest. They had minimum 14C ages of 16–27 kyr and δ13C values ranging from −24‰ to −26.5‰, indicating a terrestrial origin of organic matter. The sediments from this site were thus likely deposited by episodic mass wasting of slope sediment through the canyon, delineating the previously suggested main pathway of sediment and clay movement to abyssal Gulf sediments.  相似文献   

12.
We used a research submersible to obtain 33 sediment samples from chemosynthetic communities at 541–650 m water depths in the Green Canyon (GC) area of the Gulf of Mexico slope. Sediment samples from beneath an isolated mat of H2S-oxidizing bacteria at GC 234 contain oil (mean = 5650 ppm) and C1–C5 hydrocarbons (mean = 12,979 ppm) that are altered by bacterial oxidation. Control cores away from the mat contain lower concentrations of oil (mean = 2966 ppm) and C1–C5 hydrocarbons (mean = 83.6 ppm). Bacterial oxidation of hydrocarbons depletes O2 in sediments and triggers bacterial sulfate reduction to produce the H2S required by the mats. Sediment samples from GC 185 (Bush Hill) contain high concentrations of oil (mean = 24,775 ppm) and C1–C5 hydrocarbons (mean = 11,037 ppm) that are altered by bacterial oxidation. Tube worm communities requiring H2S occur at GC 185 where the sea floor has been greatly modified since the Pleistocene by accumulation of oil, thermogenic gas hydrates, and authigenic carbonate rock. Venting to the water column is suppressed by this sea-floor modification, enhancing bacterial activity in sediments. Sediments from an area with vesicomyid clams (GC 272) contain lower concentrations of oil altered by bacterial oxidation (mean = 1716 ppm) but C1–C5 concentrations are high (mean = 28,766 ppm). In contrast to other sampling areas, a sediment associated with the methanotrophic Seep Mytilid I (GC 233) is characterized by low concentration of oil (82 ppm) but biogenic methane (C1) is present (8829 ppm).  相似文献   

13.
The concentrations of90Sr and137Cs, derived from the radioactive fallout, in the surface layers of the adjacent seas of Japan and the North Pacific were determined radiochemically during 1969 to 1973. The90Sr and137Cs concentrations in sea water decreased markedly with increase of the depth and below the depth of 1,000 m, the concentrations were approximately uniform. The distribution of90Sr in the surface water of the North Pacific in spring of 1970 was approximately uniform, except two regions; rather large low-concentration region between 160°E and 170°W and relatively higher contamination area around 32°N and 146°W.  相似文献   

14.
Mud volcanoes, mud cones, and mud ridges have been identified on the inner portion of the crestal area, and possibly on the inner escarpment, of the Mediterranean Ridge accretionary complex. Four areas containing one or more mud diapirs have been investigated through bathymetric profiling, single channel seismic reflection profiling, heat flow measurements, and coring. A sequence of events is identified in the evolution of the mud diapirs: initially the expulsion on the seafloor of gasrich mud produces a seafloor depression outlined in the seismic record by downward dip of the host sediment reflectors towards the mud conduit; subsequent eruptions of fluid mud may create a flat topped mud volcano with step-like profile; finally, the intrusion of viscous mud produces a mud cone.The origin of the diapirs is deep within the Mediterranean Ridge. Although a minimum depth of about 400 m below the seafloor has been computed from the hydrostatic balance between the diapiric sediments and the host sediments, a maximum depth, suggested by geometric considerations, ranges between 5.3 and 7 km. The presence of thermogenic gas in the diapiric sediments suggests a better constrained origin depth of at least 2.2 km.The heat flow measured within the Olimpi mud diapir field and along a transect orthogonal to the diapiric field is low, ranging between 16 ± 5 and 41 ± 6 mW m–2. Due to the presence of gas, the thermal conductivity of the diapiric sediments is lower than that of the host hemipelagic oozes (0.6–0.9 and 1.0–1.15 W m–1 K–1 respectively).We consider the distribution of mud diapirs to be controlled by the presence of tectonic features such as reverse faults or thrusts (inner escarpment) that develop where the thickness of the Late Miocene evaporites appears to be minimum. An upward migration through time of the position of the décollement within the stratigraphic column from the Upper Oligocene (diapiric sediments) to the Upper Miocene (present position) is identified.  相似文献   

15.
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16.
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.  相似文献   

17.
The 87Sr, 13C, and 15N isotopic signatures of organic matter in sediments from the continental shelf facing the Orinoco Delta were measured to determine the contribution of sediments transported from the Amazon River by the coastal Guayana current and the sediments transported by the Orinoco River. Box core samples between 60 and 300 m water depth collected along 4 transects located eastwards to the Orinoco Delta were analyzed. Carbon and nitrogen concentrations decreased with depth under water on the shelf, and were strongly correlated indicating homogeneity of organic matter composition. Phosphorus content was also associated to organic matter in most samples, but some of them revealed deposition of P-enriched sediments. The 87Sr/86Sr ratios showed a strong continental signature averaging 0.7117, therefore, limiting the possible carbon and nitrogen sources associated with these sediments to C3 trees, C4 grasses, or freshwater phytoplankton. The δ13C values were relatively high averaging −21‰, above values reported for sediments on the Amapá shelf and the Amazon River in Brazil. Average δ13C values did not differ significantly among transects. High δ13C values point to the influence of organic matter transported from the C4-plants dominated savannas in the northern fringe of the Orinoco River. δ15N values were positive and averaged 5‰, being within the range of values measured in the Marajo island (Amazon River) and the estuary of the Pará River. The δ15N values differed significantly among transects (4.9–5.2‰), lowest values corresponding to the northernmost transect near the coast of Trinidad, and the highest values corresponding to the transect located at the southernmost position.  相似文献   

18.
The stability constants for sulfate, chloride and hydroxide ions with cerium (III) in the solution at ionic strength of 0.67 have been determined by cation exchange method, the values of 1 and 2 for sulfate complexes of cerium being 40±13 and 453±140, respectively and those for chloride complexes being 1.28±0.23 and 0.56±0.076, respectively. The values of 1, 2 and 3 for hydroxide complexes of cerium were (4.5±0.9)×107, (3.3±0.7)×1014 and (1.8±0.7)×1023, respectively.Using the above constants the ratios of individual chemical species of144Ce were calculated in a solution at ionic strength of 0.67 containing sulfate and chloride ions approximately the same as in seawater of 35 %. The result of calculation indicates that the dominant species of144Ce in this solution is Ce(OH)3 0 at pH 8.  相似文献   

19.
An automated coulometric titration system based on that described by Johnson, Sieburth, Williams and Brandstrom (1987, Mar. Chem., 21: 117–133) has been evolved for the accurate and continual measurement of total dissolved inorganic carbon (TCO2). The instrument achieves an analytical precision (1 SD) of ±0.5–1.0 μmol kg−1 (0.025–0.05%). The accuracy of the system has been examined by a limited comparison with other coulometric-based titrators and with a manometric-based system; agreement was to 1 μmol kg−1. The capability for automatic continual analysis allows surface mapping of TCO2; a sample rate of 10 analyses h−1 gives a mapping resolution of 1–2 km. Provision for frequent standardization with a liquid substandard has been included in the development. The ability to achieve high-density analyses while maintaining interlaboratory consistency and standardization constitutes a vital contribution to surveys of ocean carbon chemistry (e.g. Joint Global Ocean Flux Study, World Ocean Circulation Experiment).  相似文献   

20.
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   

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