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To estimate the atmospheric deposition flux of 210Pb in the equatorial western Indian Ocean, we determined the dissolved (<0.45 μm) and particulate 210Pb (>0.45 μm) in the water column. In addition, we calculated the atmosphere-derived dissolvable Pb in seawater using the budget of 210Pb. The dissolved 210Pb and total 210Pb were higher in the surface layer and, overall, showed a decreasing distribution with depth. In particular, radioactive 210Pb activities in the surface-to-upper layer (<1000 m depth) were 1.5 to 2 times higher than those reported in the 1970s (in nearby regions), suggesting that there has been additional 210Pb input in recent years. Based on the mass balance of the total 210Pb budget in the water column, we estimated the atmospheric deposition flux of 210Pb and the residence time of Pb for the first time in this region. The atmospheric deposition flux of 210Pb was estimated to be 0.1–0.5 dpm cm−2 yr−1, and these values agreed with the general global estimations for the major oceans (0.1–0.7 dpm cm−2 yr−1). Considering the residence time of 210Pb (29–41 years) in the water column (estimated from the 210Pb inventory and 234Th-based Pb scavenging rate), the atmospheric input of seawater-dissolvable Pb was quantified to be 0.08–0.1 nmol cm−2 yr−1, which is about eight times higher than the estimated input in the early 1990s in the region. Therefore, these results imply that radioactive 210Pb could be a useful tracer for quantifying Pb flux in seawater. [ABSTRACT FROM AUTHOR]

Highlights: What are the main findings? The first radiocesium and Pu isotopes data in Korean seas were present in 2011–2012; Higher 134Cs were observed in Korean seas immediately after the Fukushima accident; Fukushima-derived nuclides were introduced to Korean seas by the atmosphere for up to 2 months. What is the implication of the main finding? The residence times of 137Cs in Korean seas water is estimated to be 8–25 years; The dataset could be used to predict the dispersion of anthropogenic pollutant; The dataset could also be used to validate the model for future NPP accident around the Korean seas. The distributions of artificial radionuclides, radiocesium (134Cs and 137Cs) and plutonium isotopes (238Pu and 239+240Pu), in the surface water around the Korean seas (East/Japan Sea and Yellow Sea) in 2011–2012 and in three sections in the North Pacific between 2011 and 2014 were examined. The 137Cs activities in the surface water in the Korean seas in 2011 (immediately after the Fukushima nuclear power plant (NPP) accident on 17 March 2011) were comparable or not significantly different relative to those in 2010 and 2012. However, 134Cs, which had been not detected in the study area before the Fukushima accident (under the detection limit of 0.1 mBq kg−1 level), were detected rapidly in 2011 after the accident (in about 60% of the 72 samples) and gradually disappeared due to their short half-life (t1/2 = 2.06 years) in 2012 (detected in about 16% of the 24 samples). In addition, the highest activities of radiocesium and Pu isotopes appeared locally in some stations of the Korean Strait region (located between Korea and Japan) within 1–2 months immediately after the accident. This suggests that the radioactive nuclides released immediately after the Fukushima accident were significantly introduced through the atmosphere, based on recent studies conducted in neighboring areas. We also showed that the spatial distribution of radiocesium in the North Pacific moved eastward from 2012 to 2014, and we attempted to quantify the residence time of radiocesium (137Cs) in the Korean seas based on the long-term (tens of years scale) temporal trends of 137Cs activity data, which have been collected since the 1960s and 1970s. The estimated retention time of 137Cs in the East/Japan Sea and Yellow Sea were 25 ± 0.6 and 8.0 ± 0.1 years, respectively. These results are expected to be used as a preliminary study for a potential future event of a marine radioactive accident (which, of course, cannot be predicted) and as basic data for predicting the influences of radionuclide releases in the ocean. [ABSTRACT FROM AUTHOR]

We investigate the distribution of dimethyl sulfide (DMS) in the Southern Ocean's (50° W to 170° W) surface water, including the Antarctic Peninsula and the marginal sea ice zone (MIZ) in the Ross and Amundsen Seas. This is the first high-frequency observation conducted in the austral autumn (in April) in the Southern Ocean. The mean DMS concentration was 2.7 ± 2.5 nM (1 σ) for the entire study area. Noticeably enhanced DMS (5 to 28 nM) concentrations were observed in the MIZ around the Ross and Amundsen Seas and the coastal regions in the Antarctic Peninsula; this could be attributed to biological production of local ice algae, which appears to be supplied with nutrients from glacial or sea ice melt water. These observed DMS inventories were significantly higher (an order of magnitude) than current climatological DMS inventories. The local DMS sources being transported outward from the polynyas, where strong bloom occurs during summer, could result in larger discrepancies between observed DMS and climatological DMS in the MIZ area (in the Amundsen Sea). Overall, this study is the first to highlight the significance of the underestimation of current DMS fluxes in the austral autumn, which consequently results in significant errors in the climate models. [ABSTRACT FROM AUTHOR]

In whole-cell based biosensors, spectrophotometry is one of the most commonly used methods for detecting organophosphates due to its simplicity and reliability. The sensor performance is directly affected by the cell immobilization method because it determines the amount of cells, the mass transfer rate, and the stability. In this study, we demonstrated that our previously-reported microbe immobilization method, a microbe-attached single-walled carbon nanotube film, can be applied to whole-cell-based organophosphate sensors. This method has many advantages over other whole-cell organophosphate sensors, including high specific activity, quick cell immobilization, and excellent stability. A device with circular electrodes was fabricated for an enlarged cell-immobilization area. Escherichia coli expressing organophosphorus hydrolase in the periplasmic space and single-walled carbon nanotubes were attached to the device by our method. Paraoxon was hydrolyzed using this device, and detected by measuring the concentration of the enzymatic reaction product, p-nitrophenol. The specific activity of our device was calculated, and was shown to be over 2.5 times that reported previously for other whole-cell organophosphate sensors. Thus, this method for generation of whole-cell-based OP biosensors might be optimal, as it overcomes many of the caveats that prevent the widespread use of other such devices.