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1.
The distribution and inventory of artificial radionuclides,239,240Pu and137Cs were determined in the East China and the Yellow Seas in 1987. Almost all of239,240Pu and 50 to 80% of137Cs in the continental shelf area are retained in the sediment column.239,240Pu sediment inventory in the sea area is larger than the fallout input and tends to increase southwardly. This excess239,240Pu and the lateral distribution are attributable to the supply of239,240Pu by the Yangtze River discharge. On the contrary,137Cs sediment inventory shows a decrease to the south, and the fact can be accounted for by the southward dispersion of fine silt particles discharged from the Yellow River. Total137Cs inventory is smaller than the estimated fallout input, and the fact seems to indicate dispersion of137Cs out of the shelf region. Vertical profiles of239,240Pu and137Cs contents in sediments differ from that of natural210Pb, implying the effect of varied accumulation rates of the artificial radionuclides over the sediment particle mixing by benthic organisms. Apparent maximum sediment particle mixing coefficient (D B ) calculated from the excess210Pb profiles in stations located between the inner and outer shelves ranged from 1.4 to 8.3 cm2y–1. ThisD B value is higher than that in the Okinawa Trough (1.0 cm2y–1), but lower than previously estimatedD B value (26 cm2y–1) in the outer shelf mud.  相似文献   

2.
《Marine Geology》2005,216(4):249-263
Bottom sediments collected in the Northwest (NW) Pacific Ocean in 1997 were analysed for 90Sr, 137Cs, 239,240Pu and 241Am contents to determine their distribution patterns, inventories and sources. Enhanced inventories of 239,240Pu and 241Am were observed in the latitudinal belts of 10–20°N and 30–40°N, which correspond to major areas of local (tropospheric) and global (stratospheric) fallout (with a contribution from local fallout), respectively. The sediment inventory of 239,240Pu near the Bikini Atoll exceeded its overlying water inventory, however, in the mid-latitudes, more than 70% of 239,240Pu still remains in the water column. 241Am inventories in sediments exceeded that of the water column for the entire NW Pacific Ocean. Higher 137Cs and 90Sr sediment inventories in the latitudinal belt of 30–40°N are due to global fallout, and they account for about 10% and less than 5% of the water column inventories, respectively. The observed activity ratios of 137Cs/90Sr, 238Pu/239,240Pu and 241Am/239,240Pu in sediment were at some stations higher than the global fallout ratios due to contributions from local fallout and due to specific processes in the water column. Two end-member mixing model based on the 240Pu/239Pu atom ratios observed in global and local fallout yielded ∼60% contribution of the local fallout in the bottom sediments near the Bikini Atoll. The upward decrease in the 240Pu/239Pu atom ratios in the sediment column indicates a decrease in the contribution of local fallout to the Pu inventory with time. 241Am and 241Pu dating of sediment layers was utilized to explain a hiatus in sediment accumulation in the deep seafloor.  相似文献   

3.
239, 240Pu,137Cs and90Sr concentrations were determined in sea waters from the central and western North Pacific in 1980 and 1982. The results are consistent with those reported earlier for North Pacific waters. The profiles of90Sr and137Cs show a monotonic decrease with depth, whilst239, 240Pu shows a distinct subsurface maximum at a depth between 400 and 1,000 m. The calculated inventories of these nuclides significantly exceed the global mean fallout inputs for these latitudes. This may be due to local fallout input to the ocean at times of large-scale nuclear weapon tests in the equatorial North Pacific. The existence of measurable amounts of137Cs and239, 240Pu in deep waters suggests that these nuclides are transported by sinking particulate matter from the surface to the deep ocean.  相似文献   

4.
Radionuclide measurements have been conducted on sediment cores collected in 1992 in the south-eastern region of the Barents Sea, known as the Pechora Sea. Cesium-137 and 239,24OPu activities in surface sediments are generally less than 30 Bq/kg, with the highest levels being measured in sediments off the southwestern coastline of the island of Novaya Zemlya. High correlations between both 137Cs and 239,24OPu and the concentration of fine (< 63 μm) particles in surface sediments indicate that much of the variance in radionuclide concentrations throughout the Pechora Sea can be explained by particle size fractionation. However, elevated activities of 137Cs (138 Bq/kg), 60Co (92 Bq/kg), 241Am (433 Bq/kg), and especially 239,24OPu (8.47 × 103 Bq/kg) were measured in one surface sediment sample from the fjord of Chernaya Bay on the southern coast of Novaya Zemlya. The source of radioactive contamination is two underwater nuclear tests conducted in Chernaya Bay in 1955 and 1957.The 238Pu/239,240Vu activity ratio of 0.0245 in Chernaya Bay is equivalent to values measured in global fallout. The 240Pu/239Pu atom ratio (0.0304), measured by mass spectrometry, is much lower than values (0.18) typical of global fallout, but is consistent with ratios measured for fallout from the early (1951–1955) series of weapons tests at the Nevada Test Site. The timing of the Chernaya Bay source term, estimated from the 241Am/241Pu ratio, is consistent with the timing of the 1955 and 1957 underwater nuclear tests. Relatively low initial yields of 241Pu (241Pu/239Pu atom RATIO = 0.00 123) in these tests have resulted in relatively low 241Am/239,240Pu activity ratios (0.05) in recent sediments in Chernaya Bay.Radionuclide tracer profiles in cores from the Pechora Sea can be simulated using a two-layer biodiffusion model with rapid, near-homogeneous mixing in the surface mixed layer and reduced mixing in the deep layer. Lead-210 profiles are consistent with a wide range of sedimentation and mixing rates in the deep sediment layer. However, the 137Cs and 239,240Pu results further constrain the model parameters and indicate that the downward transport of radionuclides in the sediments is governed primarily by sediment mixing, with sediment burial playing a secondary role.  相似文献   

5.
The heat balance of the upper ocean under a land and sea breeze was investigated based on observations of sea water temperature in the upper 300 m layer and heat flux across the sea surface at a fixed station in Sagami Bay (3510N, 13925E) during two periods of two days in August 1980 and three days in August 1981. During both periods, a typical land and sea breeze of 4–6 m sec–1 at maximum prevailed in the observation area. Large diurnal variation of sea surface temperature with a maximum peak around noon LST was observed during both periods (the daily value of the range was 0.9C and 2.5C in 1980, and 1.2C, 1.5C and 1.7C in 1981). It was found that these large temperature variations were caused by diurnal variation of the wind speed which dropped to 0–3 m sec–1 at noon when the strongest insolation (–270 Wm–2) penetrated the sea and at midnight in association with alternations of the land breeze and the sea breeze. On the other hand, vertical mixing of the sea water caused by the wind stress and/or convection due to cooling at night extended down only to the surface 10 m layer. Horizontal heat advection was negligibly small. Therefore the local time change of the heat content in the upper 10 m water column was affected mainly by the heat flux across the air-sea interface which was estimated from data on radiation fluxes measured directly on board and latent and sensible heat fluxes calculated by the aerodynamic bulk method. The water temperature below the 10 m layer also varied with time and the temperature variation in the thermocline (20–50 m depth) was frequently larger than that of the sea surface temperature. However, the variation in the upper 10 m layer was little influenced by that below the layer.  相似文献   

6.
90Sr and137Cs concentrations and their vertical distributions were determined in deep waters in the western Northwest Pacific, including the adjacent seas of Japan, from 1976 to 1979.The profiles of the radionuclides show distribution patterns with two parts with an exponential variation of radioisotope content with depth in both parts.Generally speaking, the inventories of90Sr and137Cs in the open waters of the northwestern Pacific correspond fairly well to the fallout inputs, but in some circumstances there seems to be considerable removal of radionuclides from the water column or they are diluted with water of lower radioactivity from other regions.The possibility of radioisotope remobilization from the bottom sediment or particulate matter is also discussed.  相似文献   

7.
Arctic sea ice can incorporate sediment and associated chemical species during its formation in shallow shelf environments and can also intercept atmospherically transported material during transit. Release of this material in ice ablation areas (e.g. the Fram Strait) enhances fluxes of both sediments and associated species in such areas. We have used a suite of natural (7Be, 210Pb) and anthropogenic (137Cs, 239Pu, 240Pu) radionuclides in sea ice, sea-ice sediments (SIS), sediment trap material and bottom sediments from the Fram Strait to estimate transit times of sea ice from source to ablation areas, calculate radionuclide fluxes to the Fram Strait and investigate the role of sea-ice entrained sediments in sedimentation processes. Sea ice intercepts and transports the atmospherically supplied radionuclides 7Be and 210Pb, which are carried in the ice and are scavenged by any entrained SIS. All of the 7Be and most of the excess 210Pb measured in SIS collected in the Fram Strait are added to the ice during transit through the Arctic Ocean, and we use these radionuclides as chronometers to calculate ice transit times for individual ice floes. Transit times estimated from the 210Pb inventories in two ice cores are 1–3 years. Values estimated from the 7Be/210Pbexcess activity ratio of SIS are about 3–5 years. Finally, equilibrium values of the activity ratio of 210Pb to its granddaughter 210Po in the ice cores indicate transit times of at least 2 years. These transit times are consistent with back-trajectory analyses of the ice floes. The latter, as well as the clay-mineral assemblage of the SIS (low smectite and high illite content), suggest that the sampled sea-ice floes originated from the eastern Siberian Arctic shelf seas such as the eastern Laptev Sea and the East Siberian Sea. This result is in agreement with the relatively low activities of 239,240Pu and 137Cs and the 240Pu/239Pu atom ratios (∼0.18, equivalent to that in global fallout) in SIS, indicating that prior global atmospheric fallout, rather than nuclear fuel reprocessing facilities, forms the main source of these anthropogenic radionuclides reaching the western Fram Strait at the time of sampling (1999). Transport of radionuclides by sea ice through the Arctic Ocean, either associated with entrained SIS or dissolved in the ice, accounts for a significant flux in ablation areas such as the Fram Strait, up to several times larger than the current atmospheric flux in the area. Calculated fluxes derived from sea-ice melting compare well to fluxes obtained from sediment traps deployed in the Fram Strait and are consistent with inventories in bottom sediments. 240Pu/239Pu atomic ratios lower than 0.18 in bottom sediments from the Fram Strait provide evidence that plutonium from a source other than atmospheric fallout has reached the area. Most likely sources of this Pu include tropospheric fallout from atomic weapons testing of the former Soviet Union prior to 1963 and Pu released from nuclear reprocessing facilities, intercepted and transported by sea ice to the ablation areas. Future work is envisaged to more thoroughly understand the actual mechanisms by which radionuclides are incorporated in sea ice, focusing on the quantification of the efficiency of scavenging by SIS and the effect of melting and refreezing processes over the course of several years during transit.  相似文献   

8.
The kinetic approach ofWright andHobbie (1966) was used to determine the heterotrophic potential of Antarctic waters. Variations with depth and geographical location are discussed. Temperature studies indicate the psychrophilic nature of the microbial population. In samples having environmental temperatures of approximately –1C, significant activities were recorded at the lowest incubation temperatures tested (–3C). Activities increased with increasing incubation temperatures up to +3C but were somewhat depressed at +10C and above. By testing a wide range of substrates, qualitative differences were noted in the microbial populations of different areas.Highest rates of uptake were found in the euphotic zone whereas Vmax values of samples from depths of 500 m and below were in most cases unmeasurable.Published as Technical Paper No. 4259, Oregon Agricultural Experiment Station.  相似文献   

9.
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   

10.
The activity concentrations of dissolved137Cs have been determined in the water column and137Cs and134Cs in the sediments and the sediment porewaters of the southern Baltic Sea. The mean activity concentration of dissolved137Cs in the Gdansk Deep declined from 109 Bq m−3in June 1986 to 61 Bq m−3in 1999. In sediments, the activity concentrations of137Cs (33-231 Bq kg−1) were highest in muds and the activity concentrations of134Cs were about 6% of the total Cs activity. The Chernobyl contribution to137Cs activity was between 43% and 77%. The porewater activity concentrations of137Cs in muddy sediments were in the range 71 to 3900 Bq m−3and were higher than those in the overlying seawater. The diffusive flux of dissolved137Cs from the muddy sediments was estimated in the range 5 to 480 Bq m−2year−1. The flux of137Cs from sediment porewaters of the southern Baltic Sea was about 45% of the total, including fluxes of137Cs from wet and dry atmospheric deposition and the fluvial inputs. The results were used to elucidate the rate of recovery of the sediments and the waters of the southern Baltic from Chernobyl-derived137Cs.  相似文献   

11.
Contents of90Sr,137Cs and60Co in surface sediments were investigated in and around Urazoko Bay, Fukui Prefecture, where a nuclear power plant has been operating since 1969 and the waste effluent has been released into the sea. The main source of90Sr and137Cs was recognized to be radioactive fallout, whereas60Co was considered to originate from the nuclear power plant. Using the137Cs concentration as an indicator of sorption capacity of the sediment, the behaviour of60Co was investigated. No seasonal variation was observed in the distribution pattern of60Co/137Cs ratio and the retention of the heavy initial discharge in 1969 was considered to dominate the radionuclide level in the sediment. Correlation of60Co/137Cs ratio in the sediment and the distance from the discharge outlet was expressed by a simple exponential function of the distance. It was suggested that the contamination is spreading out gradually to the outer region of Urazoko Bay.  相似文献   

12.
The activity of photosynthesis and the contents of chlorophylla and pheo-pigments were compared in the samples of the intake and effluent seawater of Owase-Mita Thermal Power Plant and in the seawater samples in the Yoshimi Bay before and after heat treatment. At Owase-Mita Thermal Power Plant, after passage of sea water through the cooling system chlorophylla content reduced to about a half and pheo-pigment content doubled in August with high temperature (25–27C), but the contents of chlorophylla and pheo-pigments changed little in January with low temperature (16C); whereas the depression of photosynthetic activity after passing through the cooling system was 71–77 % in August and 31–46 % in January. In the laboratory experiments, the heat treatment at 34–43C for 7–8 sec., which resulted in temperature rise of 7–8C, gave the decrease of chlorophylla and an increase of pheo-pigments in August temperature (26.5C), but a slight decrease of chlorophylla and a slight increase of pheo-pigments in November at the initial temperature of 19.2C, while in January and December the samples with low initial temperature (11.6 and 10.8C) showed almost no change in the content of pigments; the decrease in photosynthetic activity was 32 % in August sample,ca. 11 % in November sample,ca. 15% in January and almost no change in December. It is concluded that the photosynthetic carbon assimilation of marine phytoplankton is suppressed by passing through the cooling system of a thermal power plant even at lower water temperature in winter, while the content of chlorophylla is affected very little at a temperature below 20C.  相似文献   

13.
Surface intertidal sediments from 35 sites in the Irish Sea have been analysed for their 238Pu and 239,240Pu activities, together with an intensive study of plutonium in sediments of the Esk Estuary (NW England). The range of plutonium activities for the whole survey were 0·14–4118 and 1·3–16 026 Bq kg−1 for 238Pu and 239,240Pu, respectively. The levels of Pu activity, derived from the Sellafield nuclear fuel reprocessing effluents, in sediments are controlled by lithological factors and the influence of transport and post-depositional processes. Grain size distribution is particularly important, the major part of plutonium activity being in the mud fraction of all sediments.The data suggest that over the Irish Sea coastline, dynamic mixing of sediment grains by reworking and resuspension and/or by dispersion in tidal currents are important in determining plutonium distributions. The exponential decrease in sediment plutonium activities away from the Sellafield source is attributed to the progressive mixing with older contaminated and uncontaminated sediments.  相似文献   

14.
Profiles of the radioisotopes 210Pb and 137Cs were determined in 15 sediment cores collected from Sagami Bay, Japan. The activities of 210Pbex (unsupported) in core top sediments increased with water depth from 25 dpm g−1 on the upper continental slope off the mouth of Tokyo Bay to an average of 283 dpm g−1 at the deep-sea station SB. The high 210Pb trapping efficiency of settling particles expected from the results of the sediment trap experiment near the SB site suggests that effective 210Pb enrichment in surface sediments may occur during resuspension and lateral transportation of particles via the benthic nepheloid layer on the continental slope. In several cores, 137Cs profiles showed an increase, a distinct peak, and then a decrease to an undetectable level downcore. These profiles can be compared with the temporal change of bomb-produced 137Cs fallout.The mean sedimentation rates estimated by the 210Pbex inventory method, rather than using 210Pbex profiles, ranged from 0.06 g cm−2 y−1 to 0.14 g cm−2 y−1. The average value of the rates in SB cores was calculated to be 0.11 g cm−2 y−1, which was similar to that calculated under the assumption that the age of the 137Cs peak corresponds to its maximum fallout year in 1963.Although 137Cs inventories represented one tenth of the anthropogenic fallout of 137Cs until 1997, they correlated with the increase in 210Pbex inventory. This suggests that the scavenging of refractory 137Cs as well as 210Pb by settling particles in the water column can lead to the formation of a time marker layer even in deep-sea sediment core, such as at the SB site.  相似文献   

15.
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.  相似文献   

16.
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   

17.
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.  相似文献   

18.
East-west vertical sections centered on Kinmei Seamount (35N, 172E) of potential temperature, salinity, and oxygen, based on recent standard hydrographic measurements, and vertical profiles ofin situ temperature and density ( 4) east of the seamount, based on STD data, show contrasting variability in the deep water characteristics east and west of the seamount. These data are consistent with horizontal variations in water mass properties (temperature-salinity and temperature-oxygen curves) east of the seamount between 2,600–3,900 m but not west of the seamount. East of the seamount on surfaces of constant potential temperature (or density) salinity and oxygen are higher at a station 200 km from the seamount than at stations on either side. From these relations and from known deep water properties of the North Pacific, it is suggested that east of the seamount, between 2,600–3,900 m, the observations are consistent with northward flow, which is interpreted to be a western boundary current with an east-west scale of about 300 km.  相似文献   

19.
The concentrations of man made radionuclides in surface seawater since early ′60s are here reported as measured in Italy and Japan. Most of the data refers to90Sr and137Cs, but occasionally the concentrations of89Sr and134Cs in some Italian samples are also given. The main sources of man made radionuclides were the global fallout produced by the nuclear weapon tests and the Chernobyl accident. The respective contributions to the contamination of surface seawater around both countries are discussed.  相似文献   

20.
The concentrations of137Cs and134Cs were measured using the sorption method in the waters of the Black Sea during 1986–1987. An inhomogeneous character of the contamination of the surface waters in the Black Sea due to the Chernobyl disaster is shown. The subsequent migration and redistribution of caesium radionuclides in the various seasons of the year were studied. The amount of137Cs and134Cs in the upper 50 m layer was estimated. The results of measuring the concentration of caesium radionuclides in the near-water atmospheric layer over the Black Sea and Mediterranean Sea in 1986–1987 are also reported.Translated by Mikhail M. Trufanov.  相似文献   

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