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Hosoda, Masahiro*; Omori, Yasutaka*; Orita, Makiko*; Saito, Kimiaki; Sanada, Tetsuya*; Takeda, Hikaru*; Tani, Kotaro*; Tsujiguchi, Takakiyo*; Hirao, Shigekazu*; Hokama, Tomonori; et al.
Hoken Butsuri (Internet), 59(4), p.206 - 207, 2024/12
no abstracts in English
Cs in a river-sea system boundary area after the Fukushima Dai-ichi Nuclear Power Plant accidentTakata, Hyoe*; Wakiyama, Yoshifumi*; Wada, Toshihiro*; Hirao, Shigekazu*; Aono, Tatsuo*; Nakanishi, Takahiro; Misono, Toshiharu; Shiribiki, Takehiko; Aoyama, Michio*
Marine Chemistry, 262, p.104384_1 - 104384_6, 2024/05
Times Cited Count:2 Percentile:24.43(Chemistry, Multidisciplinary)Yokoyama, Sumi*; Tatsuzaki, Hideo*; Tanimura, Yoshihiko; Yoshitomi, Hiroshi; Hirao, Shigekazu*; Aoki, Katsunori; Tachiki, Shuichi*; Ezaki, Iwao*; Hoshi, Katsuya; Tsujimura, Norio
Journal of Radiological Protection, 42(3), p.031504_1 - 031504_17, 2022/09
Times Cited Count:2 Percentile:30.55(Environmental Sciences)In Japan, the radiation-dose limit for the lens of the eye was revised in April 2021. Consequently, for workers, the numerical values of the equivalent dose to the lens of the eye are equal to those of the effective dose. Radiation workers, radiation safety officers and licensees must comply with regulations related to radiation protection and optimize protection. The new guidelines on dose monitoring of the lens of the eye developed by the Japan Health Physics Society recommend for the dose to be estimated near the eye for accurate estimation, when the dose to the lens approaches or exceeds the management criteria. However, there is limited information regarding the non-uniform exposure of nuclear power plant workers. In this study, the dose equivalents of high-dose-rate workplaces and the personal doses of 88 workers were estimated at four Japanese commercial nuclear power plant sites (RWR: 3 units and BWR: 3 units) and the dose to the lens of the eye and the exposure situations of the workers were analyzed.
Kuwata, Haruka*; Tazoe, Hirofumi*; Kranrod, C.*; Fujiwara, Kenso; Terashima, Motoki; Matsueda, Makoto; Hirao, Shigekazu*; Akata, Naofumi*
Radiation Protection Dosimetry, 198(13-15), p.1014 - 1018, 2022/09
Times Cited Count:0 Percentile:0.00(Environmental Sciences)Nakasone, Shunya*; Yokoyama, Sumi*; Takahashi, Tomoyuki*; Ota, Masakazu; Kakiuchi, Hideki*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; et al.
Plasma and Fusion Research (Internet), 16, p.2405035_1 - 2405035_5, 2021/02
Removal of impurities such as organic and other types of dissolved matters from environmental water samples is required for precise analysis of tritium with a liquid scintillation counting method. In general, a distillation method is a conventional one for tritium analysis in environmental water samples, but is a time-consuming process that takes 24 hours for removal of impurities. We have proposed a rapid pretreatment method for tritium analysis, that uses ion exchange resins. In this study, we performed batch experiments, to evaluate the effectiveness of the ion exchange resins on the tritium measurement. The results obtained demonstrated that removal of impurities in the sample water by ion exchange resins can be achieved during a short period of time (i.e., in 5 min).
Yokoyama, Sumi*; Ezaki, Iwao*; Tatsuzaki, Hideo*; Tachiki, Shuichi*; Hirao, Shigekazu*; Aoki, Katsunori; Tanimura, Yoshihiko; Hoshi, Katsuya; Yoshitomi, Hiroshi; Tsujimura, Norio
Radiation Measurements, 138, p.106399_1 - 106399_5, 2020/11
Times Cited Count:4 Percentile:29.78(Nuclear Science & Technology)Omori, Yasutaka*; Hosoda, Masahiro*; Takahashi, Fumiaki; Sanada, Tetsuya*; Hirao, Shigekazu*; Ono, Koji*; Furukawa, Masahide*
Journal of Radiological Protection, 40(3), p.R99 - R140, 2020/09
Times Cited Count:28 Percentile:67.69(Environmental Sciences)UNSCEAR and the Nuclear Safety Research Association report the annual effective doses from cosmic rays, terrestrial radiation, inhalation and ingestion from natural sources. In this study, radiation doses from natural radiation sources in Japan were reviewed with the latest knowledge and data. Total annual effective dose from cosmic-ray exposure can be evaluated as 0.29 mSv. The annual effective dose from external exposure to terrestrial radiation for Japanese population can be evaluated as 0.33 mSv using the data of nationwide survey by the National Institute of Radiological Sciences. The Japan Chemical Analysis Center (JCAC) performed the nationwide radon survey using a unified method for radon measurements in indoor, outdoor and workplace. The annual effective dose for radon inhalation was estimated using a current dose conversion factor, and the values were estimated to be 0.50 mSv. The annual effective dose from thoron was reported as 0.09 mSv by UNSCEAR and then the annual effective dose from inhalation can be described as 0.59 mSv. According to the report of large scale survey of foodstuff by JCAC, the effective dose from main radionuclides due to dietary intake can be evaluated to be 0.99 mSv. Finally, Japanese population dose from natural radiation can be assessed as 2.2 mSv which is near to the world average value of 2.4 mSv.
Nakasone, Shunya*; Yokoyama, Sumi*; Takahashi, Tomoyuki*; Ota, Masakazu; Kakiuchi, Hideki*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; et al.
Plasma and Fusion Research (Internet), 15, p.2405027_1 - 2405027_3, 2020/05
A quick preprocessing system for tritium analysis of environmental samples is important to judge environmental influence of tritium releases due to accident or tritium-handling facilities. Analysis of tritium in water samples with liquid scintillation counting method requires removal of impurities such as organic matter and ion species from water samples. Generally, a distillation method is adopted as a pretreatment of analysis for tritium; however, the distillation method is a time-consuming process. The aim of this study is to evaluate a rapid pretreatment method for tritium analysis with ion exchange resin. From batch and column experiments that used inland water and ion exchange resin, we confirmed removals of impurities of the water sample and that the removal of impurities was possible for a short time (by 5 minutes).
Yokoyama, Sumi*; Takahashi, Tomoyuki*; Ota, Masakazu; Kakiuchi, Hideki*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; Atarashi-Andoh, Mariko; et al.
Plasma and Fusion Research (Internet), 14(Sp.2), p.3405099_1 - 3405099_4, 2019/06
The Large Helical Device of the National Institute for Fusion Science started D-D experiments in 2017. To ensure the safety of the facility, it is important to develop evaluation methods for environmental tritium transfer. Tritiated water (HTO) in atmosphere and soil is transferred to plants, and organically bound tritium (OBT) is formed by photosynthesis. Prediction of OBT formation is important, because OBT accumulates in plants and causes dose through ingestion. The objective of this study is to estimate environmental tritium transfer using a simple compartment model and practical parameters. We proposed a simple compartment model consisting of air-soil-plant components, and tried to validate the model by comparison with a sophisticated model, SOLVEG. In this study, we plan to add wet deposition to the model and obtain parameters from measurements of soil permeability and tritium concentrations in air, soil and plants. We also establish rapid pretreatment methods for OBT analysis.
Cs from the Fukushima Daiichi Nuclear Power Plant accident; Simulations based on identical input dataSato, Yosuke*; Takigawa, Masayuki*; Sekiyama, Tsuyoshi*; Kajino, Mizuo*; Terada, Hiroaki; Nagai, Haruyasu; Kondo, Hiroaki*; Uchida, Junya*; Goto, Daisuke*; Qu
lo, D.*; et al.
Journal of Geophysical Research; Atmospheres, 123(20), p.11748 - 11765, 2018/10
Times Cited Count:58 Percentile:85.76(Meteorology & Atmospheric Sciences)A model intercomparison of the atmospheric dispersion of
Cs emitted following the Fukushima Daiichi Nuclear Power Plant accident was conducted by 12 models to understand the behavior of
Cs in the atmosphere. The same meteorological data, horizontal grid resolution, and an emission inventory were applied to all the models to focus on the model variability originating from the processes included in each model. The multi-model ensemble captured 40% of the observed
Cs events, and the figure-of-merit in space for the total deposition of
Cs exceeded 80. Our analyses indicated that the meteorological data were most critical for reproducing the
Cs events. The results also revealed that the differences among the models were originated from the deposition and diffusion processes when the meteorological field was simulated well. However, the models with strong diffusion tended to overestimate the
Cs concentrations.
I and
Cs resulting from the Fukushima Daiichi Nuclear Power Plant accidentChino, Masamichi; Terada, Hiroaki; Katata, Genki; Nagai, Haruyasu; Nakayama, Hiromasa; Yamazawa, Hiromi*; Hirao, Shigekazu*; Ohara, Toshimasa*; Takigawa, Masayuki*; Hayami, Hiroshi*; et al.
NIRS-M-252, p.127 - 135, 2013/03
We estimated the release rates and total amounts of
I and
Cs discharged into the atmosphere from March 12 to April 5, 2011. The applied method is a reverse estimation by coupling environmental monitoring data with atmospheric dispersion simulations under the assumption of unit release rate (1 Bq/h). It calculates release rates of radionuclides (Bq/h) by dividing measured air concentrations of
I and
Cs into calculated ones at sampling points. The estimated temporal variation of releases indicates that the significant release, over 10
Bq/h of
I, occurred on March 15, following to relatively small releases, 10
10
Bq/h, but the release rates from March 16 are estimated to be rather constant on the order 10
Bq/h until March 24. The release rates have decreased with small day-to-day variations to the order of 10
10
Bq/h of
I on the beginning of April. The estimated source term was examined on the point of the time trend, total releases and the ground depositions of
Cs by using different atmospheric dispersion models with above source term and compared them with observed
Cs deposition distribution. These examinations showed that the estimated source term was reasonably accurate during the period when the plume flowed over land in Japan.
Rn flux and its effect on the atmospheric
Rn concentration at Hachijo-jima island, JapanOkura, Takehisa; Yamazawa, Hiromi*; Moriizumi, Jun*; Hirao, Shigekazu*; Iida, Takao*
Hoken Butsuri, 45(3), p.270 - 277, 2010/09
Measurements of
Rn flux from the ground and
Ra content in soil were made on Hachijo-jima, which is a solitary island in the Pacific about 200 km to the south of the main island of Japan, to evaluate effect of locally exhaled
Rn to the surface air concentration of
Rn measured on this island. Averages of
Rn flux and
Ra content in dry soil were 0.88 mBq m
s
and 6.8 Bq kg
at Hachijo-jima and 9.7 mBq m
s
and 23.2 Bq kg
at Nagoya, respectively. The low level
Ra content in soil is one of main causes for the small
Rn flux at the island. With this
Rn flux, the contribution of locally exhaled
Rn from the island was estimated by a simple model to occur at concentration of 0.035 to 0.072 Bq m
(relative contribution is 4 to 12%) under typical nocturnal condition. Under diurnal condition effect is lower than that of nocturnal condition. This local
Rn component is negligible as compared with concentration of long-range transported
Rn of 0.5 to 3 Bq m
.
Okura, Takehisa; Yamazawa, Hiromi*; Moriizumi, Jun*; Hirao, Shigekazu*; Guo, Q.*; Tojima, Yasunori*; Iida, Takao*
Proceedings of 3rd Asian and Oceanic Congress on Radiation Protection (AOCRP-3) (CD-ROM), 3 Pages, 2010/05
Monitoring network of
Rn concentration in air which was measured in Beijing, Nagoya, Hegura-jima, Hachijo-jima and Hateruma-jima, as a tracer for long-range transport in East Asia was established. At inland sites, Beijing and Nagoya, high concentrations
Rn were measured, at marine sites, Hachijo-jima and Hateruma-jima,
Rn concentrations level was very low. Seasonal variations of the
Rn concentration show that
Rn concentration was the lowest in the summer and the highest in the winter. Diurnal variations were measured at inland sites. At marine sites several-day-cycle variations were measured. It was pointed out by this study that the several-day-cycle variations at Hachijo-jima were dependent on synoptic-scale atmospheric disturbance. Backward trajectory analysis of the relationship between atmospheric
Rn concentrations at Hachijo-jima and transport pathway of air mass indicates that atmospheric
Rn at Hachijo-jima has much to do with transport pathway of air.
Okura, Takehisa; Yamazawa, Hiromi*; Moriizumi, Jun*; Hirao, Shigekazu*; Guo, Q.*; Tojima, Yasunori*; Iida, Takao*
Taiki Kankyo Gakkai-Shi, 44(1), p.42 - 51, 2009/01
Monitoring network of
Rn concentration in air which was measured in Beijing, Nagoya, Hegura-jima, Hachijo-jima and Hateruma-jima, as a tracer for long-range transport in East Asia was established. At inland sites, Beijing and Nagoya, high concentrations
Rn were measured, at marine sites, Hachijo-jima and Hateruma-jima,
Rn concentrations level was very low. Seasonal variations of the
Rn concentration show that
Rn concentration was the lowest in the summer and the highest in the winter. Diurnal variations were measured at inland sites. At marine sites several-day-cycle variations were measured. It was pointed out by this study that the several-day-cycle variations at Hachijo-jima were dependent on synoptic-scale atmospheric disturbance. Backward trajectory analysis of the relationship between atmospheric
Rn concentrations at Hachijo-jima and transport pathway of air mass indicates that atmospheric
Rn at Hachijo-jima has much to do with transport pathway of air.
Cs in a river-sea system boundaryTakata, Hyoe*; Wakiyama, Yoshifumi*; Wada, Toshihiro*; Hirao, Shigekazu*; Aono, Tatsuo*; Nakanishi, Takahiro; Misono, Toshiharu; Shiribiki, Takehiko*; Aoyama, Michio*
no journal, ,
Cs emitted from Fukushima Daiichi Nuclear Power Plant; MIPs with identical source term and meteorological dataSato, Yosuke*; Takigawa, Masayuki*; Sekiyama, Tsuyoshi*; Kajino, Mizuo*; Terada, Hiroaki; Nagai, Haruyasu; Kadowaki, Masanao; Kondo, Hiroaki*; Uchida, Junya*; Goto, Daisuke*; et al.
no journal, ,
Two Model Intercomparison of Projects (MIPs) of atmospheric dispersion model targeting on
Cs released from Fukushima Daiichi Nuclear Power Plant (FDNPP) on March 2011 were conducted. Both MIPs were conducted using an identical source term of
Cs, identical meteorological data, and the same horizontal grid resolution (3 km and 1 km) to exclude the uncertainties of the model originated from them. Our analyses indicated that most of the model well simulated the atmospheric
Cs obtained from the operational aerosol sampling of the national suspended particle matter network. Our analyses also indicated that meteorological data were most critical for reproducing the atmospheric
Cs events, and the extent of the horizontal diffusion and the deposition were critical if the meteorological field was reasonably simulated. The comparison of the results between the two MIPs elucidated that the fine grid resolution is required to simulate atmospheric
Cs in the vicinity of FDNPP, but the use of the fine grid resolution does not always improve the performance of the models especially for areas distant from the FDNPP. The results of both MIPs elucidated that the good performance of some models improved the performance of the multimodel, highlighting the advantage of using a multimodel ensemble.
Cs) from the Fukushima Daiichi Nuclear Power Station Accident using identical meteorological data and source termSato, Yosuke*; Takigawa, Masayuki*; Sekiyama, Tsuyoshi*; Kajino, Mizuo*; Terada, Hiroaki; Nagai, Haruyasu; Kondo, Hiroaki*; Uchida, Junya*; Goto, Daisuke*; Qu
lo, D.*; et al.
no journal, ,
no abstracts in English
Yokoyama, Sumi*; Takahashi, Tomoyuki*; Ota, Masakazu; Kakiuchi, Hideki*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; Atarashi-Andoh, Mariko; et al.
no journal, ,
To ensure safety of fusion facilities, it is important to develop evaluation methods for tritium transfer in the environment. For estimation of tritium transfer in the terrestrial environment, we had developed a simple compartment model using the Migration Of GRound Additions (MOGRA) code. The model was composed by an air-soil-plant system. The target source terms were HT and HTO in the air. In addition, wet deposition was modeled by input of HTO to the system by rainfall. Tritium in the plant was divided into free water tritium (FWT) and organically bound tritium (OBT). The tritium concentration in the environmental medium was trial calculated for chronic and accidental HTO releases to the atmosphere, as preliminary calculation run of the model.
Kakiuchi, Hideki*; Tanaka, Masahiro*; Fukutani, Satoshi*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; Atarashi-Andoh, Mariko; Furukawa, Masahide*; et al.
no journal, ,
no abstracts in English
Hirao, Shigekazu*; Satou, Yukihiko
no journal, ,