Continuous southwestward spread of Fukushima-derived 137Cs in the subtropical western North Pacific and its intrusion flux into the South China Sea.

We provide transect profiles of 137Cs and 90Sr along 146.5°E, 136°E and 21°N in the subtropical western North Pacific (WNP) during May 2018. Exploiting the constant global fallout 137Cs/90Sr ratio, we separated Fukushima-derived 137Cs (137CsF) from background 137Cs. At most stations, 137CsF exhibited only one subsurface peak at 300 m depth, corresponding to subtropical mode water (STMW); however, at 25-28°N along 146.5°E and 25-26°N along 136°E, 137CsF exhibited two subsurface peaks, with another peak occurring at 500 m depth, corresponding to lighter central mode water (L-CMW). Temporal changes in 137CsF vertical profiles showed that 137CsF entrained by STMW has recirculated within the western subtropical gyre, while 137CsF entrained by L-CMW has turned southwestward and arrived the western basin in 2018. In the Luzon Strait, the entrance to the South China Sea (SCS), subsurface 137Cs increased since 2013 and peaked in approximately 2018. The estimated amount of 137CsF entering the SCS during 2013-2019 was 0.33 ± 0.10 PBq, equivalent to 1.7-2.2% of total leakage of 137CsF into the ocean. These results enhance our understanding of the protracted spread and fate of 137CsF in the subtropical WNP.

Fresh Groundwater Discharge as a Major Source of 90Sr into the Coastal Ocean.

The behavior and source of 90Sr in the coastal ocean remain uncertain. Here, we investigated the distributions of 90Sr in coastal fresh groundwater, river water, pore water, and seawater in three bays along the southeastern coast of China between 2019 and 2021 and evaluated the potential of submarine groundwater discharge (SGD) as a source of coastal 90Sr. The 90Sr activity in coastal fresh groundwater was higher than that in river water and seawater, while the 90Sr activity in pore water was comparable to that in adjacent seawater. In addition, nonconservative mixing behavior of 90Sr along the salinity gradient between river water and seawater was observed. These observations indicated that fresh SGD may serve as an additional source of 90Sr in coastal seawater. Combining our groundwater 90Sr data with the reported fresh SGD flux data, the estimated fresh SGD-derived 90Sr fluxes into the three bays were comparable to or even higher than those supplied by riverine sources. These results revealed that fresh SGD is a major but overlooked source of 90Sr in the coastal ocean. This subterranean pathway for transport of 90Sr to the coastal ocean should be considered in the monitoring and risk assessment of coastal areas, especially those near nuclear facilities.

90Sr in seawater of the East China Sea: Inventory, new potential source, and environmental implications.

90Sr is useful for tracing water mass movement in oceans. We collected a suit of seawater samples from the East China Sea (ECS) in the May 2011 to investigate the spatial and vertical distribution of 90Sr and to understand its transportation and fate. To understand the sources and transportation of 90Sr more clearly, published 137Cs data from the same cruise were used to obtain the 90Sr/137Cs activity ratios. The results showed that 90Sr activities were controlled by the circulation system of the ECS, with high values in coastal regions and low values in oceanic waters. The plume with a high 90Sr/137Cs ratio showed that in late spring, the Changjiang Diluted Water could flow southeastward and extend to 126-127° E, which is farther than the previously known value of 124° E. The high 90Sr/137Cs ratios (1.35 ± 0.62) and a long effective half-life of 90Sr (20.0 ± 0.3 y) in the ECS surface water revealed that 90Sr is surplus in comparison with 137Cs. However, historical variations in the 90Sr/137Cs ratio seem to preclude the simple explanation that riverine input causes a 90Sr surplus in the ECS. Groundwater discharge with a high 90Sr but very low 137Cs may be a new potential source. However, it is difficult to quantify the contribution of groundwater discharge at present, and more detailed studies are required in this regard. Additionally, we compiled 90Sr and 137Cs water column inventory data in the western North Pacific and found that the cumulative fallout onto the ocean was different from that on land in the 20-40° N band.

222Rn, 210Pb and 210Po in coastal zone groundwater: Activities, geochemical behaviors, consideration of seawater intrusion effect, and the potential radiation human-health risk.

Groundwater quality in human-influenced coastal landscapes is receiving novel attention. Radionuclides have been recognized as another important monitoring indicator in many developed countries due to the discovery of extremely high level of natural 210Po (up to 10,000 Bq/m3) and radium and radon isotopes. This study aims to evaluate the groundwater quality in the Beibu Bulf-Guangxi coast from radiological point of view. 210Po, 210Pb and 222Rn activities in 20 wells ranged from 0.24 ± 0.05 to 6.96 ± 1.62 Bq/m3, 2.17 ± 0.12 to 13.08 ± 0.74 Bq/m3 and 1500 ± 200 to 31,800 ± 900 Bq/m3, respectively. Compared with research data of other countries, groundwaters in this area have 210Po, 210Pb and 222Rn activity within low levels. The large deficiencies of 210Po and 210Pb relative to 222Rn in groundwaters implied that 210Po and 210Pb are strong particle-reactive radionuclides and they might be controlled by similar scavenging processes in groundwaters due to a good positive correlation between 210Pb and 210Po (R2 = 0.67, p < 0.01). The concentrations of 210Po and 210Pb decreased with increasing pH values and salinity, which indicated that geochemical behaviors of 210Po and 210Pb in groundwater were influenced by seawater intrusion and pH changing. Groundwater 222Rn activity concentrations decreased with increasing salinity in coastal zone, which may be caused by dilution due to seawater intrusion or intensified 222Rn escaping from well-developed pores in coastal zone. The estimated annual ingestion doses for infants, children and adults were well below the recommended reference dose level (RDL) of 0.2-0.8 mSv/a, suggesting that consumption of analyzed groundwaters is safe from radiological point of view.

Accumulation of natural and anthropogenic radionuclides in body profiles of Bryidae, a subgroup of mosses.

Mosses can be used as biomonitors to monitor radionuclide deposition and heavy metal pollution in cities, forests, and grasslands. The aims of this work were to determine the activity concentrations of natural (210Po, 210Pb or 210Pbex (excess 210Pb is defined as the activity of 210Pb minus the activity of 226Ra), 7Be, 40K, 226Ra, 238U, and 232Th) and anthropogenic radionuclides (137Cs) in moss body profiles and in situ underlying soils of moss samples and to assess/determine the distribution features and accumulation of these radionuclides. Activity concentrations of radionuclides in the samples were measured using a low-background gamma spectrometer and a low-background alpha spectrometer. Consistent with their source, the studied radionuclides in the moss samples and underlying soils were divided according to the principal component analysis (PCA) results into an airborne group (210Po, 210Pb (210Pbex), 7Be, and 137Cs) and a terrestrial group (40K, 238U, 226Ra, and 232Th). The activity concentrations of 210Po and 210Pbex in moss body profiles were mainly concentrated in the stems-rhizoid parts, in which we measured some of the highest 210Po and 210Pbex levels compared to the results in the literature. 7Be mainly accumulated in the leaves-stem parts. Different positive correlations were observed between 210Po and 210Pb and between 7Be and 210Pb, which indicated that the uptake mechanisms of 210Po, 210Pb, and 7Be by moss plants were different, to some extent. 137Cs was detected only in some moss samples, and the fraction of 137Cs in the underlying soils was much lower than that in the moss, suggesting that mosses were protecting the underlying soils from further pollution. Except for 40K, the terrestrial radionuclide (238U, 226Ra, and 232Th) content in mosses was predominantly at low levels, which indicated not only the inability of mosses to use those elements for metabolic purposes but also the rather poor capability of mosses to directly mobilize, absorb, and transport elements (U, Ra, or Th) not dissolved in water.

Distribution of 137Cs in the Bohai Sea, Yellow Sea and East China Sea: Sources, budgets and environmental implications.

The transport processes and fate of 137Cs in eastern Chinese seas (ECSs) that consists of the Bohai, Yellow, and East China Seas, have not been well established. In this study, we measured the concentrations of 137Cs in the ECSs water and surface sediments during 2013-2014. Combined with a number of published 137Cs inventory data from drainage basins and sediment accumulation rates in the ECSs, the distribution, sources and budgets of 137Cs in the ECSs were investigated. The 137Cs activity in the water column and surface sediments ranged from 0.03 to 1.92 Bq/m3 and from 0.30 to 5.22 Bq/kg, respectively. No 134Cs signal was observed, suggesting that the Fukushima accident had limited impact on the ECSs during the investigation period. Mass balance of 137Cs suggests that at least 7.4 × 1012 Bq/y of 137Cs imported into the ECSs from the Northwestern Pacific that accounts for 0.7% of the 137Cs transported by the Kuroshio Current, and this value is 5.2 times higher than the sum of atmospheric fallout and total riverine input. The apparent half-lives of 137Cs are estimated to be 15.1 y for the ECS and 7.7 y for the YS. The vertical profiles in the continental shelf edge and the Yangtze River Estuary reveal that the upwelling of the Kuroshio Subsurface Water is the main mechanism of 137Cs import into the ECSs. The high level of 137Cs in oceanic water masses and the low level of 137Cs in riverine and coastal waters make 137Cs a good indicator for tracing water mass movement and interaction. In addition, good correlation between 137Cs activity and mean grain size (φ) indicates that 137Cs can serve as an effective tracer to track dispersal pathways of fine sediments in river-dominated marginal seas.