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1.
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   

2.
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   

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.
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   

5.
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   

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.
Anthropogenic 90Sr, 239,240Pu and 241Am were used as tracers of water mass circulation in the Crozet Basin of the South Indian Ocean, represented by three main water fronts—Agulhas (AF), Subtropical (STF) and Subantarctic (SAF). Higher 90Sr concentrations observed north of 43°S were due to the influence of AF and STF, which are associated with the south branch of the Subtropical gyre, which acts as a reservoir of radionuclides transported from the North to the South Indian Ocean. On the other hand, the region south of 43°S has been influenced by SAF, bringing to the Crozet Basin Antarctic waters with lower radionuclide concentrations. The 238Pu/239,240Pu activity ratios observed in water and zooplankton samples indicated that, even 35 years after the injection of 238Pu to the Indian Ocean from the burn-up of the SNAP-9A satellite, the increased levels of 238Pu in surface water and zooplankton are still well visible. The radionuclide concentrations in seawater and their availability to zooplankton are responsible for the observed 210Po, 239,240Pu and 241Am levels in zooplankton.  相似文献   

8.
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   

9.
We report here thermal ionization mass spectrometry measurements of 239Pu, 240Pu, 241Pu, 242Pu, and 237Np isolated from oceanic, estuarine, and riverine sediments from the Arctic Ocean Basin. 238Pu/239+240Pu activity ratios are also reported for alpha spectrometric analyses undertaken on a subset of these samples. Our results indicate that the Pu in sediments on the Alaskan shelf and slope, as well as that in the deep basins (Amerasian and Eurasian) of the Arctic Ocean, has its origin in stratospheric and tropospheric fallout. Sediments from the Ob and Yenisei Rivers show isotopic Pu signatures that are distinctly different from those of northern-hemisphere stratospheric fallout and indicate the presence of weapons-grade Pu originating from nuclear fuel reprocessing wastes generated at Russian facilities within these river catchments. Consequently, sediments of the Eurasian Arctic Ocean, particularly those in the Barents and Kara Seas, probably contain a mixture of Pu from stratospheric fallout, tropospheric fallout, and fuel-reprocessing wastes of riverine origin. In particular, the 241Pu/239Pu ratios observed in these sediments are inconsistent with significant contributions of Pu to the arctic sediments studied from western European reprocessing facilities, principally Sellafield in the UK. Several other potential sources of Pu to arctic sediments can also be excluded as significant based upon the transuranic isotope ratios presented.  相似文献   

10.
The Neuse River estuary is part of the large Albemarle/Pamlico estuarine/lagoonal system (APES) of North Carolina. Exchange between the APES and the open ocean is restricted to inlets in the Outer Banks barrier islands. Freshwater discharge of the Neuse River is low in relation to the size of its estuary, so that the estuary is normally brackish over most of the area which accumulates fine-grained sediments. Mud (silt + clay) accumulation rates are low ( 6 mm year−1).From the mud distribution and the dynamics of suspended sediment in the estuary it has been inferred that the Neuse retains fines efficiently, with probable episodic (high discharge) losses seaward, to Pamlico Sound.As part of a study of particle transport, deposition, and accumulation in the Neuse estuary, we have collected radiochemical data (10 cores) and chemical data (seven cores) on sediment cores from the main channel of the estuary between New Bern, North Carolina and the estuary mouth. K/Al increases in the lower estuary, consistent with earlier reports of increasing illite in the clay fraction. Landward transport of sediment from Pamlico Sound is the most plausible explanation for the increasing K/Al (illite). A marine sediment source may, therefore, be important for the lower estuary.The distribution of sediment inventories (quantities per cm2 of sediment column) of particle-reactive radionuclides is consistent with the hypothesis of landward sediment transport. Inventories of excess 210Pb, 137Cs, and 239,240Pu are coherent through the estuary and show the effects of particle redistribution processes on regionally uniform inputs. To obtain excess (anthropogenic) Zn and Cu, we use metal/Al normalization to estimate natural backgrounds. Anthropogenic metal inputs are concentrated at the head of the estuary, and sediment inventories of excess Zn and Cu generally decrease seaward. Normalization of the excess Zn and excess Cu inventories to excess 210Pb inventories corrects the raw metal inventories for effects of lithology and sediment redistribution. The normalized excess Zn inventory decreases smoothly seaward, while the normalized excess Cu inventory shows an unexplained mid-estuary maximum. Low normalized inventories of anthropogenic metals at the estuary mouth indicate that little modern riverine sediment is stored there.Increasing K/Al (illite) and decreasing anthropogenic Zn and Cu in the lower estuary are thus both consistent with a predominantly marine sediment source. We conclude that landward transport of muds from Pamlico Sound has contributed significantly to the sediment balance of the lower Neuse estuary.  相似文献   

11.
黄亚楠 《海洋学报》2022,44(11):77-87
本文对东海及毗邻海域中239+240Pu比活度、240Pu/239Pu原子比值和239+240Pu累积通量或沉积通量数据进行整理,首次从大气沉降、海水中、生物体中、沉积物捕获器中以及沉积物中的239+240Pu 5个方面阐述了东海及毗邻海域中239+240Pu的地球化学行为。研究结果表明,全球大气沉降和太平洋核试验场输入的239+240Pu是东海海水和沉积物中239+240Pu的两个主要来源;在长江径流、浙闽沿岸流、台湾暖流、黑潮与上升流等水团的混合作用以及清除作用的影响下,东海近岸海水中239+240Pu浓度在时间上呈现被清除而减少的趋势,相应近岸浅水区沉积物中239+240Pu的埋藏深度高于远岸深水海域。在黑潮入侵和上升流的作用下,冲绳海槽区尤其是台湾岛东北部,沉积物中的239+240Pu比活度与沉积通量显著增大。同时,利用东海表层沉积物中239+240Pu比活度和240Pu/239Pu原子比值的相关关系证实了台湾东北部黑潮底层分支流的存在,并指示出台湾暖流与黑潮底层分支流可能交汇的海域位置。  相似文献   

12.
Laboratory experiments were carried out to assess the role of photochemical reactions upon the dissolution of 239 + 240pu and 241Am from marine sediment in sea water. Supplementary information was obtained by comparing their behaviour with that of 54Mn under similar experimental conditions. Irradiation from natural sunlight resulted in more than a ten-fold increase in the extent of 239 + 240Pu desorption relative to that observed in the dark. Remobilisation of 54Mn from sediment was also enhanced by natural sunlight, albeit to a lesser extent than 239 + 240Pu, whilst the behaviour of 241Am was largely unaffected. Data for concentrations of dissolved 239 + 240Pu(IV) and 239 + 240Pu(V) species showed that only the oxidised form was significantly affected by irradiation, indicating remobilisation occurs as a result of photooxidation reactions. Further experiments were carried out using artificial light sources to establish the influence of wavelength. Data from these investigations indicated 239 + 240Pu photooxidation (hence desorption) was a function of both light intensity and wavelength. Remobilisation decreased concomitant with light intensity but increased as the wavelength decreased. Similar trends were observed for photoreduction of 54Mn, although differences were less pronounced than those observed for 239 + 240Pu.  相似文献   

13.
241Am is a useful tracer for understanding biogeochemical processes in the marine environment. 241Am also poses a potential radiation threat to human health due to the continuous increase of its concentration in the global environment. We report a rapid analytical method for determining 241Am in marine sediments using isotope dilution sector-field inductively coupled plasma mass spectrometry (SF-ICP-MS) combined with a high-efficiency sample introduction system (APEX-Q). A selective CaF2 co-precipitation procedure followed by TRU extraction chromatography was employed to effectively remove the major sediment matrix and to pre-concentrate 241Am. We achieved an extremely low detection limit of 0.32 fg/g or 0.041 mBq/g (for 1 gram sediment), which is better than that of alpha spectrometry, and it allowed the accurate determination of 241Am in low-level marine sediment samples. The accuracy and precision of the developed analytical method was evaluated using a laboratory prepared Am isotope standard solution and Ocean Sediment reference material (IAEA-368). The results were satisfactory. For sediment samples, overall chemical recoveries varied from 60–90%. The developed method was applied to the study of 241Am depth distribution in Sagami Bay, Japan, where we observed different depth profiles between 241Am activity and 239+240Pu activity.  相似文献   

14.
《Marine Chemistry》2001,73(2):125-152
We report here bioturbation and sediment accumulation rates determined from replicate sediment cores at four different sampling sites on the Palos Verdes shelf, Southern California, using bomb fallout and natural radionuclides (137Cs, 239,240Pu, 210Pb, 234Th, and 14C), along with supporting measurements of organic carbon (OC), porosity and granulometry. Present-day particle reworking, on time scales of several months, is restricted to the upper 3 cm, with rates ranging from 13 to 200 cm2/year, as deduced from 234Thxs profiles. There is little evidence that particle reworking reached depths significantly greater than 5 cm. Post-1963 (or post-1971) sediment accumulation rates ranged from 0.7 to 1.4 g/cm2/year (equivalent to 1.1–1.8 cm/year for surficial sediments), as calculated from Pu and Cs isotope profiles, with little change over time or distance from the outfall. Lateral transport of older sediment and multiple sediment sources on the Palos Verdes shelf is suggested from radiocarbon measurements on foraminifera and bulk sedimentary organic matter at two sampling sites, which showed variable, old and refractory sources of OC. Pre-1953 sediments accumulated at rates that were at least 0.4 g/cm2/year (≥0.3 cm/year), based on 210Pbxs dating. Given the abundance of sediment sources to the Palos Verdes shelf, the high sedimentation rates, and shallow particle mixed layers, contaminant-enriched layers should continue to move deeper into the sediments.  相似文献   

15.
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   

16.
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   

17.
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   

18.
The discharge of radioactive waste, from nuclear fuel reprocessing facilities, into the coastal waters of north-west Europe has resulted in a significant increase in the inventories of a number of artificial radionuclides in the North Atlantic. Radiocaesium, 90Sr and 99Tc, which behave conservatively in seawater, have been used widely as tracers of water movement through the North Sea, Norwegian Coastal Current, Barents Sea, Greenland Sea, Fram Strait, Eurasian Basin, East Greenland Current and Denmark Strait overflow. These studies are summarised in the present paper. It has been estimated that 22% of the 137Cs Sellafield discharge has passed into the Barents Sea, en route to the Nansen Basin, via the Bjomoya-Fugloya Section, with another 13% passing through the Fram Strait. This amounts to 14 PBq 137Cs. Quantifying the influx of other radionuclides has been more problematic. The inflowing Atlantic water now appears to be diluting waters in the Arctic Basin, which were contaminated in the late 1970s and early 1980s as a result of the substantial decrease in the discharge of reprocessing wastes. Sellafield (U.K.) has dominated the supply of 134Cs, 137Cs, 90Sr, 99Tc and Pu, whereas La Hague (France) has contributed a larger proportion of 129I and 125Sb.  相似文献   

19.
Investigations including a bathymetric survey, sonic prospecting, and vibrocoring were performed to understand the horizontal and vertical distribution of 137Cs in seabed sediments in shallow seas with depths less than 30 m near the Fukushima Daiichi Nuclear Power Plant. Especially, features of 137Cs distributions in deeper sections of the seabed sediments were studied to evaluate the vertical heterogeneity of 137Cs distribution in the seabed sediments in shallow seas. The distribution area of the seabed sediments was less than half of the investigation area, and the locations of the seabed sediments were divided into flat and terrace-like seafloors based on their topographical features. The thicknesses of the seabed sediment layers were mostly <2 m. The 137Cs inventories in the seabed sediments varied from 13 ± 1 to 3,510 ± 26 kBq m?2, and continuous distributions of 137Cs at depths greater than 81 cm were observed. The 137Cs distributions were not uniform; however, the 137Cs inventories tended to be larger near the base of the steeper ascending slopes than in the terrace-like seafloors themselves. Based on the relationship between the 137Cs inventories and mean shear stress, features of the seafloor topography were inferred to be significant control factors governing the horizontal and vertical distribution of 137Cs in the seabed sediments. Rapid changes and multiple peaks in the vertical profile of the 137Cs distributions suggest that they are related to pulse input caused by heavy-rain events. Change in the 137Cs inventories with depth in this study are larger than those reported in previous studies, indicating earlier results of 137Cs inventories per unit in seabed sediments in shallow seas, especially near the river mouth, which drains a radiologically highly-contaminated basin, were underestimated.  相似文献   

20.
Sediment cores were collected from the shelf, slope, and basin of the Bering, Chukchi, and Beaufort Seas during May–June (under ice cover) and July–August (largely ice-free) 2004. Measurements of chlorophyll a (chl a), total organic carbon (TOC), and C/N ratios were made in surface and some subsurface core increments. Surface sediment chl a decreased with increasing water depth. Significant positive correlations were found between chl a and TOC and chl a and C/N ratios in the basin (>2000 m), but there were significant negative correlations between chl a and C/N ratios on the shelf (⩽200 m). Chl a values generally declined in down-core profiles, but in some deeper slope and basin cores, measurable inventories of subsurface chl a were present at depth. In some cases, these subsurface chlorophyll inventories coincident with peak activities of the anthropogenic radionuclide 137Cs were detected, which had maximal deposition following the atmospheric nuclear weapons testing era in the 1960s. A sedimentation rate independently determined for one of these cores using 210Pb was consistent with the depths of subsurface 137Cs peaks in slope sediments reflecting steady, relatively undisturbed deposition over a several-decade period. The depth of penetration of 137Cs in some continental slope sediments, together with detectable chl a, suggests that chl a can be buried in some of these deeper-water sediments under cold conditions for decadal periods in the absence of deposit feeders. Because organic deposition from the water column is episodic at high latitudes and concentrated following the spring bloom, these buried sources of organic materials, whether on the shelf or in deeper basin sediments, may ultimately be important for benthic invertebrates that could utilize this food source during times of the year when primary production flux from the overlying water column is reduced.  相似文献   

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