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BACKGROUND: This article summarizes the methodology, results, and challenges of the reconstruction of red bone marrow and male breast doses for a 1982-person sub-cohort of ∼114,270 U.S. military veterans who participated in eight atmospheric nuclear weapons tests between 1945 and 1962. These doses are being used in an epidemiological investigation of leukemia and male breast cancer as part of a study of one million U.S. persons to investigate risk from chronic low-dose radiation exposure. METHODS: Previous doses to these veterans had been estimated for compensation and tended to be biased high but newly available documentation made calculating individual doses and uncertainties using detailed exposure scenarios for each veteran possible. The techniques outlined in this report detail the methodology for developing individual scenarios and accounting for bias and uncertainty in dose based on the assumptions made about exposure. RESULTS: Doses to the atomic veterans in this sub-cohort were relatively low, with about two-thirds receiving red bone marrow doses <5 mGy and only four individuals receiving a red bone marrow dose >50 mGy. The average red bone marrow dose for members of the sub-cohort was 5.9 mGy. Doses to male breast were approximately 20% higher than red bone marrow doses. DISCUSSION AND CHALLENGES: Relatively low uncertainty was achieved as a result of our methodology for reconstructing exposures based on knowledge of the individual veterans' locations and activities from military records. Challenges did arise from use of military records to determine probability of participation in specific activities but accounted for in estimates of uncertainty.

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BACKGROUND: The United States (U.S.) conducted 230 above-ground atmospheric nuclear weapons tests between 1945 and 1962 involving over 250,000 military personnel. This is the first quantitative assessment of asbestos-related mesothelioma, including cancers of the pleura and peritoneum, among military personnel who participated in above-ground nuclear weapons testing. METHODS: Approximately 114,000 atomic veterans were selected for an epidemiological study because they were in one of eight series of weapons tests that were associated with somewhat higher personnel exposures than the other tests and because they have been previously studied. We were able to categorize specific jobs into potential for asbestos exposure based on a detailed database of the military activities of the atomic veterans. Standardized mortality ratios (SMR) were calculated by service, rank (officer/enlisted) and ratings (occupation code and work location aboard ship) after 65 years of follow-up. RESULTS: Mesothelioma deaths were significantly increased overall (SMR 1.56; 95% CI 1.32-1.82; n = 153). This increase was seen only among those serving in the PPG (SMR 1.97; 95% CI 1.65-2.34; n = 134), enlisted men (SMR 1.81; 95% CI 1.53-2.13; n = 145), and the 70,309 navy personnel (SMR 2.15; 95% CI 1.80-2.56; n = 130). No increased mortality rates were seen among the other services: army (SMR 0.45), air force (SMR 0.85), or marines (SMR 0.75). Job categories with the highest potential for asbestos exposure (machinist's mates, boiler technicians, water tender, pipe fitters, and fireman) had an of SMR 6.47. Job categories with lower potential (SMR =1.35) or no potential (SMR =1.28) for asbestos exposure had non-significantly elevated mesothelioma mortality. CONCLUSIONS: The large excess of mesothelioma deaths seen among atomic veterans was explained by asbestos exposure among enlisted naval personnel. The sources of exposure were determined to be on navy ships in areas (or with materials) with known asbestos content. No excess of mesothelioma was observed in other services or among naval personnel with minimal exposure to asbestos in this low-dose radiation exposed cohort.

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BACKGROUND: Approximately 235,000 military personnel participated at one of 230 U.S. atmospheric nuclear weapons tests from 1945 through 1962. At the Nevada Test Site (NTS), the atomic veterans participated in military maneuvers, observed nuclear weapons tests, or provided technical support. At the Pacific Proving Ground (PPG), they served aboard ships or were stationed on islands during or after nuclear weapons tests. MATERIAL AND METHODS: Participants at seven test series, previously studied with high-quality dosimetry and personnel records, and the first test at TRINITY formed the cohort of 114,270 male military participants traced for vital status from 1945 through 2010. Dose reconstructions were based on Nuclear Test Personnel Review records, Department of Defense. Standardized mortality ratios (SMR) and Cox and Poisson regression models were used in the analysis. RESULTS: Most atomic veterans were enlisted men, served in the Navy at the PPG, and were born before 1930. Vital status was determined for 96.8% of the veterans; 60% had died. Enlisted men had significantly high all-causes mortality SMR (1.06); officers had significantly low all-causes mortality SMR (0.71). The pattern of risk over time showed a diminution of the 'healthy soldier effect': the all-causes mortality SMR after 50 years of follow-up was 1.00. The healthy soldier effect for all cancers also diminished over time. The all-cancer SMR was significantly high after 50 years (SMR 1.10) primarily from smoking-related cancers, attributed in part to the availability of cigarettes in military rations. The highest SMR was for mesothelioma (SMR 1.56) which was correlated with asbestos exposure in naval ships. Prostate cancer was significantly high (SMR 1.13). Ischemic heart disease was significantly low (SMR 0.84). Estimated mean doses varied by organ were low; e.g., the mean red bone marrow dose was 6 mGy (maximum 108 mGy). Internal cohort dose-response analyses provided no evidence for increasing trends with radiation dose for leukemia (excluding chronic lymphocytic leukemia (CLL)) [ERR (95% CI) per 100 mGy -0.37 (-1.08, 0.33); n = 710], CLL, myelodysplastic syndrome, multiple myeloma, ischemic heart disease, or cancers of the lung, prostate, breast, and brain. CONCLUSION: No statistically significant radiation associations were observed among 114,270 nuclear weapons test participants followed for up to 65 years. The 95% confidence limits were narrow and excluded mortality risks per unit dose that are two to four times higher than those reported in other investigations. Significantly elevated SMRs were seen for mesothelioma and asbestosis, attributed to asbestos exposure aboard ships.

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Plutonium (Pu) has attracted attention as an environmental tracer due to its radiotoxicity and the possibility of sources linked with nuclear accidents in recent years. Plutonium isotopes (239,240Pu) were detected at trace levels in soils collected from the Xinjiang region located between the Semipalatinsk nuclear test site and China's Lop Nor nuclear test site. Little is known regarding the spatial variation of 239,240Pu in soils from this region. This study reports the use of Sector Field Inductively Coupled Plasma Mass Spectrometry (SF-ICP-MS) methods to distinguish between Pu isotopes derived from global fallout and nuclear weapon tests. We found that the 239,240Pu activity concentrations ranged from 0.035 to 1.338 mBq/g; the 240Pu/239Pu atomic ratios were 0.157-0.223 with a weighted average of 0.180 ± 0.002, corresponding with the expected average global fallout ratio of 0.180 ± 0.014. This indicated that global fallout is the major source of Pu in the study region. The 239,240Pu inventories in these soils ranged from 23.67 to 222.7 Bq/m2, corresponding with those from other areas in China and other countries within the latitude range. Our Pu isotope data was supplemented with other published Pu data for soils collected in the vicinity of the Semipalatinsk nuclear test site and Lop Nor nuclear test site. Results indicate that 239,240Pu inventories and 240Pu/239Pu atomic ratios in soils exhibit large variations with distance from the Semipalatinsk nuclear test site. High deposition and accumulation of Pu, and low 240Pu/239Pu ratios were observed in close-in fallout and downwind regions of the Semipalatinsk nuclear test site and China's Lop Nor nuclear test site.

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The 240Pu/239Pu atom ratios were determined by inductively coupled plasma mass spectrometry for seawater samples from the Okinawa Trough in the western North Pacific Ocean margin to identify their Pu sources and to elucidate the temporal variability in atom ratios in the water columns in the western North Pacific Ocean and its marginal seas. The 239Pu, 240Pu and 239+240Pu water column inventories were 12.2 ± 0.5, 10.5 ± 0.5 and 22.7 ± 0.7 Bq m-2, respectively. The observed 240Pu/239Pu ratios were clearly greater than the mean global fallout ratio of ∼0.18 with a mean value of 0.236 ± 0.014. The observed greater atom ratios confirmed the presence of close-in fallout Pu from nuclear testing at the Pacific Proving Grounds (PPG). The relative percentage of the PPG-derived Pu to global fallout Pu was estimated as 41 ± 10%. The 239+240Pu water column inventory originating from the PPG close-in fallout was also calculated as 9.2 ± 0.4 Bq m-2. The temporal variability in the mean 240Pu/239Pu atom ratios in the water columns in the western North Pacific Ocean and its marginal seas was obtained through comparison of the present study values and the previously reported values, and it had no significant temporal variation with a mean value of 0.237 ± 0.004 during the observation period of 1984-2015. The 239Pu and 240Pu derived from the two different sources of global fallout and the close-in fallout at the PPG were homogenized in the water masses in the studied areas.

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The 240Pu/239Pu atom ratios in seawater from the northern North Pacific Ocean and Bering Sea were determined to elucidate the temporal variability in 239+240Pu inventory, to identify their Pu sources and to propose the transport pathway of Pacific Proving Grounds (PPG)-derived Pu into the studied area. Water column 239+240Pu inventory in the Bering Sea was lower than that reported for a comparable station in the Geochemical Ocean Sections Study, indicating that the Bering Sea inventory has been decreasing at the average rate of 2.6 Bq m-2 yr-1. The 240Pu/239Pu atom ratios ranged from 0.222 to 0.255 with a mean value of 0.235 in the northern North Pacific Ocean and from 0.215 to 0.237 with a mean value of 0.224 in the Bering Sea. The obtained 240Pu/239Pu ratios were clearly higher than the mean global fallout ratio of 0.18. These high atom ratios proved the presence of close-in fallout Pu from nuclear weapons testing at the PPG. The relative contribution of the global fallout and the PPG fallout were evaluated by using the two-end-member mixing model. The 239+240Pu inventories originating from the PPG fallout were calculated as 17.9-25.4 Bq m-2 in the northern North Pacific Ocean and 11.6-16.6 Bq m-2 in the Bering Sea, which corresponded to 38-54% and 31-45% of the total 239+240Pu inventory in the water column in the northern North Pacific Ocean and Bering Sea, respectively. A significant amount of the PPG-derived Pu has been transported to the northern North Pacific Ocean and Bering Sea. The proposed transport pathway accounting for the high 240Pu/239Pu ratio in the Bering Sea water column is the transportation of PPG-derived Pu by the North Equatorial Current followed by the Kuroshio Current, Kuroshio Extension, North Pacific Current and subsequently the Alaska Current, and then the Alaskan Stream.

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A new methodology of time series analysis has been tested on 133Xe and estimated 220Rn activity concentrations in order to characterise the site response of four different CTBT/IMS monitoring stations. Seasonal variability of 133Xe and 220Rn at these IMS stations and the role played by different meteorological parameters on such variability have been quantified. As xenon and radon are both noble gases with similar physical characteristics but very different source terms, the methodology adopted in this comparative study, once coupled to analysis of radioxenon emission time series sampled at nearby NPPs or IPFs and to direct measurements of 220Rn at IMS sites location, might help assess relative influence of near and far field air on IMS radioxenon detections. Possible applications of the adopted methodology to radioxenon categorisation schemes are also discussed.

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We made an assessment of the levels of radionuclides in the ocean waters, seafloor and groundwater at Bikini and Enewetak Atolls where the US conducted nuclear weapons tests in the 1940's and 50's. This included the first estimates of submarine groundwater discharge (SGD) derived from radium isotopes that can be used here to calculate radionuclide fluxes in to the lagoon waters. While there is significant variability between sites and sample types, levels of plutonium (239,240Pu) remain several orders of magnitude higher in lagoon seawater and sediments than what is found in rest of the world's oceans. In contrast, levels of cesium-137 (137Cs) while relatively elevated in brackish groundwater are only slightly higher in the lagoon water relative to North Pacific surface waters. Of special interest was the Runit dome, a nuclear waste repository created in the 1970's within the Enewetak Atoll. Low seawater ratios of 240Pu/239Pu suggest that this area is the source of about half of the Pu in the Enewetak lagoon water column, yet radium isotopes suggest that SGD from below the dome is not a significant Pu source. SGD fluxes of Pu and Cs at Bikini were also relatively low. Thus radioactivity associated with seafloor sediments remains the largest source and long term repository for radioactive contamination. Overall, Bikini and Enewetak Atolls are an ongoing source of Pu and Cs to the North Pacific, but at annual rates that are orders of magnitude smaller than delivered via close-in fallout to the same area.