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1.
A method is described for the determination of Th isotopes (232Th,230Th,228Th and227Th) in seawater through analysis of Th adsorbed on MnO2-impregnated fiber that has been moored in the deep sea for up to 10 months. Since the MnO2-fiber adsorbs Th from seawater at a constant rate, natural234Th can be used as a yield monitor by making a correction for its decay during the period of deployment. The results obtained by the method showed good reproducibility and accuracy. The method has the advantage over the chemical coprecipitation method that the time and labor for sampling and processing a large-volume of seawater is reduced.  相似文献   

2.
Distribution of 230Th and 231Pa in the water column was measured in the Eurasian basins of the Arctic Ocean, i.e. the Makarov, Amundsen and Nansen basins. The profiles obtained were compared to one previously published from the Alpha Ridge (Bacon et al., Earth and Planetary Science Letters, 95 (1989) 15–22. The Amundsen and Nansen basins are similar in their 23OTh and 231Pa distribution, whereas in the Makarov Basin and at the Alpha Ridge these radionuclides are comparatively enriched in the deep basin. This may be due to low particle flux in conjunction with low water mass renewal rates. The 230Th concentration in water depth < 1000 m in the Makarov Basin is relatively low compared with the Alpha Ridge, which may be caused by an exchange of water masses between the Amundsen and Makarov basins.In the Eurasian Basin Deep Water, 230Th profiles can be explained both by a scavenging model and by a mixing-scavenging model. Enhanced particle load caused by resuspension may explain the increased scavenging in the Eurasian Basin Bottom Water. The differences in scavenging between the Norwegian-Greenland Sea and the Eurasian basins at present are not large enough to cause significant fractionation between 230Th and 231Pa.  相似文献   

3.
The contents of plutonium isotopes (239Pu and238Pu), thorium isotopes (232Th,230Th and228Th) and protactinium-231 in sea water collected in the North Pacific, the East China Sea and the Japan Sea were determined. These nuclides were sequentially analyzed byα-ray spectrometry after separating them mainly with solvent extraction technique. The contents of239Pu in surface sea water ranged from 0.6 to 1.6 pCi/10001,238Pu/239Pu activity ratios being 0.2～0.7. The228Th/232Th activity ratios for the North Pacific waters varied between 7.6 and 30, whereas the sample from the East China Sea showed the very high value, 65. The contents of231Pa are less than 6 percent of that in equilibrium with its parent235U. Furthermore, the analysis of plutonium isotopes in recent coral from Yoron Island was carried out and it was confirmed that plutonium isotopes have concentrated in recent coral with the concentration factor of about 1～2×103.  相似文献   

4.
We report the role of particle composition and lateral particle movement that influences the oceanic distribution of 231Pa and 230Th. Settling particles were collected during sediment trap experiments. These and surface sediments were obtained from five stations along 38 to 44°N in the northwestern North Pacific. The high total mass flux and seasonal variations in the marginal area of the western North Pacific are controlled by the supply of lithogenic materials and primary productivity. The high content of the lithogenic material in the settling particles in this area contributes to 230Thex fluxes that exceed the local rate of supply. The lithogenic materials are important as a carrier of 230Th and contribute to the fractionation between 230Th and 231Pa in the ocean, as the 231Paex/230Thex ratio in the settling particles decreases with increasing 232Th concentration. The 231Paex/230Thex ratio in the settling particles collected in the abyssal basin decreases with water depth, which indicates that lateral transport of the lithogenic particles from the marginal area and/or shallower depth plays an important role in determining the 231Paex/230Thex ratio in a population of settling particles and remineralization. This indicates that lateral redistribution of particles and sediment focusing influence the 231Paex/230Thex ratios in surface sediments. Thus, the observations reported here mean that the use of the sediment 231Paex/230Thex ratio as a paleoproductivity proxy will be problematic in the northwestern North Pacific. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

5.
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   

6.
Five manganese nodules collected from the Northern Mid - Pacific have been analysed for their U and Th isotopes.lt is found that the enrichment of thorium compared to uranium is universal in deep- sea manganese, nodules and in the top sides of the nodules there are large excesses of Th and Pa decreasing exponentially with depth. For each of the nodules, the concordant growth rates are obtained from three different methods: 230Thex 230Thex/232Th and 231Paex.The growth rates of manganese nodules are closely related to the chemical compositions of the nodules and the types of the underlying sediments. The growth rates of five nodules are determined to be in the range of 0.79-7.4 mm/106a, in agreement with those predicted from the chemical compositions of the nodules. By the comparison of the extrapolated 230Thex,230Thex/232 Th and 231PaeX data from the top and bottom surfaces of the nodule from Site M21 yields, the nodule turnover time is (9.83-13.7)×104a.  相似文献   

7.
Distribution and flux of234Th,232Th and230Th in the water column of central Santa Monica basin observed over a period of seven years show seasonal and interannual variabilities. A steady-state model is applied to the integrated data to calculate long term average flux and model rate constants of Th isotopes. Mass balance calculations show that the basin acts like a closed system for short-lived234Th, but not for the long-lived isotopes230Th and232Th. Most230Th in the basin is transported from elsewhere. Of the incoming Th, 40–55% of the230Th and 14–26% of the232Th enter the surface water in dissolved form. In the upper 100 m, the residence time of dissolved Th with respect to adsorption onto suspended particulates, 70–80 days, is about one order of magnitude higher than the residence time of suspended particles with respect to aggregation into sinking particles, 7–10 days.  相似文献   

8.
Dissolved and particulate samples were collected to study the distribution of thorium isotopes (234Th, 232Th and 230Th) in the water column of the Indian sector of the Southern Ocean (from 42°S to 47°S and from 60°E to 66°E, north of the Polar Front) during Austral summer 1999. Vertical profiles of excess 230Th (230Thxs) increases linearly with depth in surface water (0–100 m) and a model was applied to estimate a residence time relative to the thorium scavenging (τscav). Low τscav in the Polar Front Zone (PFZ) are found, compared to those estimated in the Subtropical Front Zone (STZ). Changes in particle composition between the PFZ and STZ could influence the 230Thxs scavenging efficiency and explain this difference. An innovative coupling between 234Th and 230Thxs was then used to simultaneously constrain the settling velocities of small (0.6–60 μm) and large (above 60 μm) particles. Although the different hydrological and biogeochemical regimes visited during the ANTARES IV cruise did not explain the spatial variation of sinking velocity estimates, our results indicate that less particles may reach the seafloor north (60 ± 2 m d− 1, station 8) than south of the Agulhas Return Current (119 ± 23 and 130 ± 5 m d− 1 at stations 3 and 7, respectively). This information is essential for understanding particle transport and by extension, carbon export. In the deep water column, the 230Thxs concentrations did not increase linearly with depth, probably due to lateral transport of North Atlantic Deep Water (NADW) from the Atlantic to the Indian sector, which renews the deep waters and decreases the 230Thxs concentrations. A specific 230Thxs transport model is applied in the deep water column and allows us to assess a “travel time” of NADW ranging from 2 to 15 years.  相似文献   

9.
The concentration of thorium isotopes and the activity ratios of230Th/232Th and228Th/232Th in sea water collected in the Kuroshio region, the mixing area of Oyashio and Kuroshio, the Japan Sea and the East China Sea in the western North Pacific were determined. Thorium isotopes were analyzed by α-ray spectrometry after separating them with an anion exchange resin. The average content of thorium (232Th) of 2.2×10−9 g/l was obtained in the open Pacific waters. The ratio of230Th/232Th is in accord with that of the top layer of the sediment in the same area. The high values of228Th/232Th ratio up to 36 were observed in sea water. The excess228Th in sea water may be due to the migration of228Ra through the water-sediment interface. Thorium content in suspended matter was 10 to 20% of the total thorium content in the Pacific water.  相似文献   

10.
Each about 400 l of seawater sample was collected in the northern North Pacific and filtered through a membrane filter. Four radioisotopes of thorium,232Th,230Th,228Th and234Th, were determined for the two FractionsF (filtrate) andP (particles on the filter). In the percentages of FractionP in the subsurface water,230Th was significantly larger than other 3 isotopes, and232Th was significantly smaller than other 3 isotopes. The former finding can be explained by the slower rates in the reversible change between the FractionsF andP. The latter one, however, cannot be explained if thorium isotopes in the FractionF are truly dissolved with the same chemical form. This suggests that major part of the FractionF of232Th is not identical with those of other radiogenic thorium isotopes, and it should not be composed of simple dissolved ions. The removal of radiogenic234Th was related to the biological activity, but there was a deviation, between the FractionP and radioactivity deficiency of234Th in their vertical profiles. The deviation was similar to that between the chlorophylla and phaeo-pigments contents including their maximum depths.  相似文献   

11.
In order to estimate the deposition rate of extraterrestrial material onto a manganese crust in a search for supernova debris, we analyzed the contents of 10Be, 230Th, 231Pa, and 239,240Pu in a sample of manganese crust collected from the North Pacific Ocean. On the basis of the depth profile of 10Be, the growth rate of the manganese crust was determined to be 2.3 mm Myr−1. The uptake rates of 10Be, 230Th, and 231Pa onto the manganese crust were estimated to be 0.22–0.44%, 0.11–0.73%, and 1.4–4.5%, respectively, as compared to the deposition rates onto the deep-sea sediments near the sampling station, while that for 239,240Pu was 0.14% as compared to the total inventory of seawater and sediment column. Assuming that sinking particles represent 0.11–4.5% of the uptake rates, the deposition rate of extraterrestrial material onto the manganese crust was estimated to be 2–800 μg cm−2Myr−1 according to the uptake of 10Be onto the manganese crust. Further, our estimate is similar to the value of 9–90 μg cm− 2Myr−1 obtained using the integrated global production rate of 10Be and the deposition rate of 10Be onto the manganese crust.  相似文献   

12.
This article summarizes the author's work on210Pb and210Po distributions in the marine environment for which the Okada Prize of the Oceanographical Society of Japan was awarded. In this review, the work of other investigators and the studies now going on are also included. The210Pb concentration in the surface water of the ocean is controlled by the atmospheric flux of210Pb and productivity. The disequilibrium between226Ra and210Pb in the deep sea reveals that the oceanic residence time of lead is less than a hundred years rather than of the order of thousands of years as thought before based on stable lead measurement in ocean water. Particulate removal of210Pb from the water column is likely to be the major cause of the deficiency of210Pb in the water, however more investigations would be needed to clarify the detailed removal mechanism of210Pb. The experiments on particulate flux by using sediment traps will provide an unique opportunity to examine this. 210Pb in excess of226Ra in sediment is useful for geochronology of shallow water sediments and the study on bioturbation rates on the deep sea sediments.  相似文献   

13.
234Th is a particle-reactive radionuclide widely used to trace biogeochemical oceanic processes occurring over short timescales. During the last few years, small-volume techniques based on the co-precipitation of 234Th with MnO2 coupled with beta-counting have been developed as an alternative to large volume gamma-spectrometric techniques. Here a procedure has been developed to enhance quantitative measurement of 234Th in MnO2 precipitates. The main objectives were to obtain a purified Th fraction for beta-counting and to determine the chemical recovery of 234Th using Th spikes and alpha-spectrometry as an alternative to ICP-MS based methods. Two variations of the procedure are presented. In the first “1 spike” method a 230Th tracer is added to the sample prior to precipitation of MnO2, and UTEVA® extraction chromatography is used to obtain a NdF3(Th) purified source that can be used for both beta-counting of 234Th and alpha-spectrometry of 230Th. In the “2 spike” method a 230Th spike is added and the MnO2(Th) precipitate is directly beta-counted for 234Th and subsequently spiked with 228Th or 229Th prior to UTEVA® purification and alpha-spectrometry. The results confirm the need to process small-volume seawater samples for 234Th measurement in presence of a yield tracer, and show that both the 1 spike and 2 spike methods allow an accurate and precise determination of 234Th (relative percent difference, RPD, between expected and mean measured value < 1%; CV between replicate samples < 3%). Our work also suggests that, although the combined analytical uncertainty on total 234Th measurements accomplished with both versions of the NdF3 procedure is promising (6% for 2-L samples), the precision of the 234Th flux estimation will ultimately depend on the degree of disequilibrium between 234Th and 238U.  相似文献   

14.
90Sr,106Ru, natural strontium and major elements were studied in 12 samples of beach deposits from Togi, Fukuura and Shiga, and in 26 samples of shallow water sediments from sea off Fukuura, Noto Peninsula, Ishikawa Pref., Japan.The average contents of natural strontium and90Sr in the beach deposits were 488 ppm ranging from 247 to 1,550 ppm and 45±9 pCi kg–1-dry mud ranging from 18 to 72 pCi kg–1-dry mud, respectively. While the average contents of natural strontium,90Sr and106Ru in the sediments were 234 ppm ranging from 136 to 415 ppm, 22±6 pCi kg–1-dry sand ranging from 7 to 48 pCi kg–1-dry sand and 0.6 ±0.2 nCi kg–1-dry ranging from 0.3 to 1.2 nCi kg–1-dry, respectively.The average contents of each natural strontium and90Sr in the beach deposits were about two times higher than those in the shallow water sediments. But no obvious relation of natural strontium to90Sr was found in all the samples. The enrichment of90Sr and108Ru in the beach deposits or tthe sediments were as high as 150320 and of 2,0003,000 compared with average contents of90Sr and106Ru in a liter of surface water from the Japan Sea. It is to be noticed that the average106Ru to90Sr ratio of 27 for the shallow water sediments is much higher than the average of 1.0 for surface sea water of the Japan Sea.As to major elements of the samples, the beach deposits are rich in silicon (Av. 70.89 ±0.92% SiO2), but poor in iron (Av. 2.99±0.32% Fe2O3). Whereas the shallow water sediments are poor in silicon (Av. 52.96±10.33% SiO2) and rich in iron (Av. 5.50±1.90% Fe2O3), calcium (Av. 9.64±9.22% CaO) and magnesium (Av. 2.83±1.58% MgO).  相似文献   

15.
A record of radionuclide fluxes at a deep marginal sea of the Northwest Pacific Ocean (39°40′N 132°24′ E, Japan Basin, East Sea/Sea of Japan) was obtained from analysis of a 1-year continuous collection of sediment-trap samples. The trap was placed at a depth of 2800 m, 500 m above the sea floor, and the samples were recovered at the end of one year. Concentrations of 238U, 234U, 232Th, 230Th and 228Th were measured in the trapped material. All of the radionuclide fluxes showed seasonal variations that were in phase with the variations in total particle flux, which were shown in earlier work to be closely tied to the primary production in the surface water. The formation of authigenic 238U appears to be less than in other open ocean regimes. The residence time of particulate thorium isotopes were of the order of a year, resulting in an average settling rate of a meter per day. Comparison of the measured 230Thex flux with that of the theoretical production in the overlying water column yielded about 40% surplus of 230Th, indicating that lateral advection contributes 230Th to this sampling site.  相似文献   

16.
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   

17.
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18.
Sediment trap experiments were carried out in two oceans, the eastern Pacific Ocean and the Antarctic Ocean, which have very different biological productivities. The natural radionuclides,234Th,210Po and210Pb were used as tracers of reactive metals. Larger particulate fluxes of these radionuclides were found in the seas where total mass fluxes were larger, although the concentrations of these radionuclides in the settling particles were somewhat smaller. The concentrations of234Th in the settling particles varied widely and irregularly with depth, whereas the concentrations of210Po and210Pb in the settling particles steadily increased with increasing water depth. The ratios of210Po/210Pb in the settling particulates were larger than unity which the ratio of234Th/excess210Po as larger than234Th/210Po in the deep water. These results suggest that, when the particles sink through the water column, these radionuclides are being absorbed by settling particles in the order234Th>210Po>210Pb. The observed particulate fluxes of210Pb are about one eighth of those calculated from the disequilibria between226Ra and210Pb at the stations in the subtropical eastern Pacific, although the observed fluxes are the same as the calculated ones in the northern North Pacific and the Antarctic Ocean. Thus, there must be a horizontal flow carrying these reactive metals from the oligotorophic ocean to the biologically productive ocean where the metals are removed by settling particles even in deep water.  相似文献   

19.
《Oceanologica Acta》1998,21(3):469-484
Presented here is the first detailed geochemical data set on the U/Th series Th, Pa, Ac, and Pb isotopes and artificial fallout radionuclides (90Sr, 137Cs, and Pu isotopes), and some trace elements (V, Zn, Cd, Cu, Mn, and Ni) in two water columns of the Japan and Bonin trenches down to the bottom depths of 7585 m and 9750 m, respectively. Hydrographic properties such as temperature, salinity, dissolved oxygen, and nutrient content within the trench valley remain constant at the same levels as those in the bottom water of the Northwest Pacific basin (typically ∼6000 m in depth). The radionuclide activities and most trace metal concentrations are also not very different from those in the overlying water at depths of around 5000–6000 m. This means that any chemical alteration which sea water undergoes during its residence within the trench was not obviously detected by the techniques used here. The suggestion follows that the trench water is rather freely communicating by isopycnal mixing with the bottom water overlying the Northwest Pacific abyssal plain. The trench waters contain high 239, 240Pu activities throughout, indicating that Pu is actively regenerating from rapidly sinking, large particles at the bottom interface, probably due to a change in the oxidation state. On the other hand, the vertical profiles of 210Pb and 231Pa show lower activities within the trench than those in the overlying deep waters, suggesting that the effect of boundary and bottom scavenging is significant in controlling their oceanic distributions. However, none of the trace metals studied here obviously follows the behaviour of the above nuclides. The 228Th data show scattering within the Bonin Trench that is largely ascribable to analytical errors. If, however we accept that the scatter of 228Th data is real and the variation is caused solely by decay of its parent 228Ra, we can set an upper limit of ∼5 years for the renewal time of the trench water.  相似文献   

20.
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   

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