Development of methodology for identification and assessment of ecosystems with an underground source of tritium.

The article considers the issues of working out the suitable approaches for identifying zones with the presence of underground near-surface waters with increased concentrations of tritium discharged into a surface reservoir. The following methods were used as possible methods: determination of tritium content in snow cover, determination of tritium content in vegetation in the form of tritium of free water and organically bound tritium, determination of tritium content in river water and coastal vegetation. The studies were carried out at a previously identified site where groundwater with a tritium concentration of up to 6000 Bq/l is present, located in the vicinity of the city of Obninsk (Kaluga region, Russia). As a result of the conducted research, it was concluded that the analysis of the distribution of tritium in vegetation is an excellent methodological technique for identifying areas of location of near-surface underground waters contaminated with tritium. As a control parameter, both the concentration of tritium in the free water of plants and the content of organically bound tritium can be used. To detect underground tritium contamination the most promising use is the following indicator - the content of OBT in the shoots of woody plants. This parameter is very informative, and the sampling procedure for its determination has no seasonal restrictions, unlike such parameters as the content of tritium in grass and leaves, the content of tritium in snow cover, surface waters, which are preferably collected only in summer or winter. It should be noted that the control of surface waters of the groundwater discharge zone may not be a sufficiently informative indicator for identifying areas of polluted water inflow, since it depends on the ratio of the volumes of leaking polluted groundwater and the annual flow of the watercourse.

Evaluation of Deuterium Oxide Deposition Velocity over a Forest Environment.

ABSTRACT: Field experiments were performed to evaluate the deposition velocity of tritium oxide within a forest environment at the Savannah River Site near Aiken, SC. Field releases were designed to guide selection of deposition velocity values for use in safety-basis modeling. Six releases of deuterium oxide were conducted in 2020 and 2021 with corresponding air samples during and following each release. Samples were analyzed to determine the deuterium-to-hydrogen ratio in water and converted to concentrations of deuterium in the air during the experiment. Measurements were compared to prior model simulations to evaluate model performance and deposition velocity estimates. Field releases demonstrated vertical and horizontal mixing of a plume in a forest. Predicted deposition velocities ranged from 2.4 to 5.4 cm s -1 on average. In all cases, model simulations underpredicted deuterium concentration by 1 to 2 orders of magnitude, indicating the model does not sufficiently mix the plume into the forest. While the model underestimated the transfer of material downward through the forest, it does suggest that the model's estimates are conservative for making downwind dose estimates because of lower plume depletion, leading to higher concentration and dose estimates. While the field releases do not cover all possible meteorological conditions, we conclude it is appropriate to use a non-zero deposition velocity when performing safety-basis modeling of tritium oxide based on conservatism within the model. A recommendation of 1.0 cm s -1 as a deposition velocity is made, which is beyond the 95 th percentile value estimated from the prior modeling study.

Use of tritium in characterizing the leachate migration from a landfill - Central de tratamento de resíduos sólidos (CTRS) BR040 (Belo Horizonte, Minas Gerais, Brazil).

Landfills often become a source of environmental impact due to the percolation of the leachate (liquid resulting from the decomposition of buried waste), which can eventually disperse and contaminate the soil and water bodies. This study aimed to evaluate quantitatively and spatially the leachate plume from the former Belo Horizonte landfill in the Coqueiros and Taiobas watersheds by using tritium (3H) concentration in nineteen (19) sampling points: 14 groundwater, 4 surface water and 1 leachate. Among the methodologies applied to determine the 3H content in the leachate, pre-filtration proved to be the most effective due to the ease treating of the sample, as well as the identical results obtained compared to the traditional method. The 3H contents resulted in concentrations up to thirty times higher in the leachate (=96,19 to 111,87 TU) and ten times in groundwater (PM23/3 = 45,06 TU), compared to the calculated threshold (TS) of rainfall tritium (TS_3Hrain = 3,41 TU). Temporal series results indicate no trend and no influence of seasonality regarding the entry of pluvial tritium, leachate liquid level and wells water level. The 3H contour maps shows a transport of the mixture (water and leachate) towards the Coqueiros stream, with a higher concentration of leachate in wells closer to the landfill slope (PM13, PM14, PM15, and PM23) and in the southwest margin of the Coqueiros stream (PM17). In the furthest portion of the landfill, 3H levels are higher than the base threshold only at the deepest level of PM20 (=3,90 TU), possibly due to factors such as: i) denser character of the leachate compared to groundwater; ii) greater influence of recharge for regions further away from the landfill slope; and iii) the presence of the rock about 50 m from the surface. Based on the hydrogeological conceptual model, the transport of the leachate water mixture in the groundwater water compartment of the Coqueiros watershed basin seems to follow a piston or dispersion flow, with a small Peclet number (Pd = 0,05, as an example), as indicated by the high correlation coefficient values (R2 ≈ 0,85 to 0,99) from graphic interpolation. The mixture of water and leachate results in a transient time (tt) ≈ 30 years and linear velocity (Vl) ≈ 3-14 m/year in the interpolated sections. These indicate a coherent correlation with the mean hydraulic conductivity (K ≈ 29,34 m/year), as they result in effective porosity values between (Ne) ≈ 0.16 to 0.36, which corresponds to Ne range for unconsolidated sediments, similar to the wells lithotype profiles. Time series evaluation combined with lumped parameter approach suggest to be an interesting way to better understanding the HCM, and, therefore, to determine hydrodynamic parameters using tritium as a tracer.

Influence of irrigation approaches and spatial geolocation on tritium speciation, uptake and depuration.

Pine needles and tree cores from a tritium (T) contaminated phytoremediation forest at the Savannah River Site (SRS in Aiken, SC) Mixed Waste Management Facility (MWMF) were measured for total T and T speciation and compared to other locations at the SRS and the surrounding area. Tree core ages ranged from 9 to 14 years old, covering over half of the ∼20-year on-going remediation efforts, while pine needles represent more recent time periods of 1-to-2-year increments. Remedial irrigation efforts at the MWMF are found to directly influence the pine needle T concentrations. The T content in the MWMF samples is higher than non-irrigated needle samples from other locations around the SRS. Further, the different forms of organic bound T are preferentially stored in tree core tissue, compared to pine needles where tritiated water dominates.

Analysis of environmental biological effects and OBT accumulation potential of microalgae in freshwater systems exposed to tritium pollution.

The ecological risk of tritiated wastewater into the environment has attracted much attention. Assessing the ecological risk of tritium-containing pollution is crucial by studying low-activity tritium exposure's environmental and biological effects on freshwater micro-environment and the enrichment potential of organically bound tritium (OBT) in microalgae and aquatic plants. The impact of tritium-contaminated wastewater on the microenvironment of freshwater systems was analyzed using microcosm experiments to simulate tritium pollution in freshwater systems. Low activity tritium pollution (105 Bq/L) induced differences in microbial abundance, with Proteobacteria, Bacteroidota, and Desulfobacterota occupying important ecological niches in the water system. Low activity tritium (105-107 Bq/L) did not affect the growth of microalgae and aquatic plants, but OBT was significantly enriched in microalgae and two aquatic plants (Pistia stratiotes, Spirodela polyrrhiza), with the enrichment coefficients of 2.08-3.39 and 1.71-2.13, respectively. At the transcriptional level, low-activity tritium (105 Bq/L) has the risk of interfering with gene expression in aquatic plants. Four dominant cyanobacterial strains (Leptolyngbya sp., Synechococcus elongatus, Nostoc sp., and Anabaena sp.) were isolated and demonstrated good environmental adaptability to tritium pollution. Environmental factors can modify the tritium accumulation potential in cyanobacteria and microalgae, theoretically enhancing food chain transfer.

Development of a Novel Passive Monitoring Technique to Showcase the 3D Distribution of Tritiated Water (HTO) Vapor in Indoor Air of a Nuclear Facility.

Tritiated water (HTO), a ubiquitous byproduct of the nuclear industry, is a radioactive contaminant of major concern for environmental authorities. Although understanding spatiotemporal heterogeneity of airborne HTO vapor holds great importance for radiological safety as well as diagnosing a reactor's status, comprehensive HTO distribution dynamics inside nuclear facilities has not been studied routinely yet due to a lack of appropriate monitoring techniques. For current systems, it is difficult to simultaneously achieve high representativeness, sensitivity, and spatial resolution. Here, we developed a passive monitoring scheme, including a newly designed passive sampler and a tailored analytical protocol for the first comprehensive 3D distribution characterization of HTO inside a nuclear reactor facility. The technique enables linear sampling in any environment at a one-day resolution and simultaneous preparation of hundreds of samples within 1 day. Validation experiments confirmed the method's good metrological properties and sensitivity to the HTO's spatial dynamics. The air in TU Wien's reactor hall exhibits a range of 3H concentrations from 75-946 mBq m-3 in the entire 3D matrix. The HTO release rate estimated by the mass-balance model (3199 ± 306 Bq h-1) matches the theoretical calculation (2947 ± 254 Bq h-1), suggesting evaporation as the dominant HTO source in the hall. The proposed method provides reliable and quality-controlled 3D monitoring at low cost, which can be adopted not only for HTO and may also inspire monitoring schemes of other indoor pollutants.

Environmental airborne tritium monitoring system based on absorption of tritiated water on calcium chloride.

Environmental monitoring of tritium around nuclear facilities is conducted in order to demonstrate compliance with regulatory requirements on the protection of members of the public. Multiple techniques are used to monitor its concentration in air, soil and flora. A new monitoring system was developed, which is based on the absorption of tritiated water on Calcium Chloride grains. Calcium Chloride has an improved capability to absorb water vapor, compared with other absorbents/adsorbents: it can absorb water vapor as much as three times its own weight. The Calcium Chloride is inserted inside a plastic bag where it interacts with environmental vapor through a membrane filter "window". The tritium absorption rate is then controlled by adjusting the free area of the membrane filter. After the determination of the tritium activity absorbed in the calcium chloride using a liquid scintillation system, a model is used to estimate its airborne concentration, considering the environmental conditions.

Transit time estimation of drying springs in Uttarakhand region using environmental tritium concentration.

Many parts of the Uttarakhand state, situated in the hilly terrain of the Himalayan region of India are facing acute water crisis due to the drying up of the perennial springs which are the only source of potable water in those regions. Tritium (3H), the radioactive isotope of hydrogen (half-life of 12.32 years) and also a part of water molecule (in the form of HTO) acts as a very useful tracer in estimating the transit time of the hydrological systems. Tritium concentrations of three springs (S-1, S-2 and S-3) were monitored consecutively for three years (2017-2019) to better constrain the transit time estimation. The tritium concentrations of the springs are found to vary between 3.66 and 4.15 TU. All the springs show gradual decrease in tritium concentration with the passage of time indicating the diminishing percentage of freshly recharged modern water component. Among various lumped parameter models, the piston-flow model (PFM), exponential mixing model (EMM), exponential piston-flow model (EPM) and partial exponential mixing model (PEM) have been employed in this study. The historical record of weighted mean concentration of tritium in precipitation available for the Uttarakhand region is taken as input function in the modelling procedure. The application of various LPMs (PFM, EMM, EPM and PEM) indicates that the transit time of the S-1 spring ranges from 1.26 to 1.46 years whereas for S-2 spring, the transit time is found to vary from 5 months to 1.1 years. The MTT of S-3 spring ranges from 5 months to 11 months. The relatively short residence time of these springs indicates the actively recharged system. The estimation of accurate transit time is thus very crucial for understanding the renewability of the spring water systems.

Toward an efficient determination of tissue-free water tritium in food.

Introduction: Tritium in the environment constitutes a radiological concern because it can become part of the hydrogen pool in environmental and biological reservoirs and thereby expose people to radiation. Methods: Tissue-free water tritium (TFWT) analysis in food is an important subject of environmental radiation monitoring which plays an important role in the estimation of health risks from environmental tritium exposure. At present, tritium content in food is generally determined by liquid scintillation counter (LSC). To improve the analytical efficiency in tritium determination, we developed a novel method to treat TFWT in food using microporous membranes. Results: The microporous membrane treatment method developed in this study has the following characteristics: It has a wide range of application and can process TFWT samples with conductivity below 5 µS/cm. Sample loss for the microporous membrane treatment is approximately 5%. The average treatment time is only 5 min, significantly shortened compared with the currently used atmospheric distillation treatment method (1.5 h). The results of the comparison and spike experiment show that the samples prepared by microporous membrane treatment provides equally satisfactory tritium measurement results as classic distillation method. Discussion: The developed microporous membrane method is simple to operate, efficient, and environmentally friendly, and effectively improves the analysis efficiency of TFWT in food.

Distribution of hydrogen isotope in the soil around the Qinshan Nuclear Power Plant.

When a different types of reactor are operating at the same area and the same period of time, released radionuclides are hard to follow in the environment. In general, isotopic techniques can be used for source localization. To obtain the distribution of hydrogen isotope in soil, eight sampling points were selected along the local dominant wind direction with different distances away from Qinshan Nuclear Power Plant, and soil samples at different depths (0-2, 2-5, 5-10, 10-20, 20-30 cm) were collected in December 2019 and December 2020, respectively. The concentrations of hydrogen isotopes were measured in the soil samples at different depth. The spatial distribution of tritium and deuterium in the surface soil was related to soil properties and the distance from the nuclear power plant. It was found that tritium and deuterium are generally enriched in the upper layer. Determination of the deuterium concentration in the environment may be a new way to trace the released tritium from the reactors.

Impact of the Fukushima Accident on 3H and 14C Environmental Levels: A Review of Ten Years of Investigation.

The investigation of the impact of the Fukushima accident is still going on although more than ten years have passed since the disaster. The main goal of this paper was to summarize the results of tritium and radiocarbon determinations in different environmental samples, possibly connected with the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident. A document containing compiled data may serve as a solid basis for further research in the selected fields. To accomplish such effort, we went through dozens of relevant published papers, reporting 3H and 14C activity concentrations in precipitations, groundwater, seawater, river systems, tree rings, and, in some more extraordinary samples, such as herbaceous plants or debris from the damaged reactor buildings. As the referenced results would not be obtainable without adequate analytical techniques, the most common methods for routine measurement of tritium and radiocarbon concentrations are discussed as well. We believe that the correct identification of the affected environmental compartments could help quantify the released 3H and 14C activities and track their following fate, which could be especially important for plans to discharge contaminated water from the FDNPP in the upcoming years.

Assessing tritium contamination in Thailand's rainwater: A study of environmental monitoring and nuclear surveillance.

Tritium, whether naturally occurring or caused by human nuclear activity, can result in a large amount of tritium contamination in the environment, especially in the water cycle, causing a high concentration of tritium in rainfall. The objective of this research was to measure the level of tritium in the environment from rainfall in two different areas as a basis for monitoring tritium contamination in the environment. Rainwater samples were collected in Thailand every 24 h for a period of 1 year during 2021-2022 at the Kasetsart University Station, Sriracha Campus, Chonburi province and at the Mae Hia Agricultural Meteorological Station, Chiang Mai province. The tritium levels were measured in rainwater samples using the electrolytic enrichment method combined with liquid scintillation counting. The chemical composition of the rainwater was analyzed based on ion chromatography. The results (presented with ± combined uncertainty) showed that the tritium content in the rainwater samples at Kasetsart University Station Sriracha Campus was in the range 0.9 ± 0.2-1.6 ± 0.3 TU (0.11 ± 0.02-0.19 ± 0.03 Bq.L-1). The mean concentration was 1.0 ± 0.2 TU (0.12 ± 0.03 Bq.L-1). The most common ions found in the rainwater samples were SO42-, Ca2+, and NO3-, with mean concentrations of 1.52 ± 0.82, 1.08 ± 0.51, and 1.05 ± 0.78 mg.L-1, respectively. The tritium content in rainwater collected from the Mae Hia Agricultural Meteorological Station was in the range 1.6 ± 0.2-4.9 ± 0.4 TU (0.19 ± 0.02-0.58 ± 0.05 Bq.L-1). The mean concentration was 2.4 ± 0.4 TU (0.28 ± 0.05 Bq.L-1). The most common ions found in the rainwater were NO3-, Ca2+, and SO42-, with mean concentrations of 1.21 ± 1.02, 0.67 ± 0.43, and 0.54 ± 0.41 mg.L-1, respectively. The tritium concentration in the rainwater at both stations differed but remained at a natural level (less than 10 TU). There was no correlation between the tritium concentration and the chemical composition of the rainwater. The tritium levels obtained from this study could be used as a basis for reference and monitoring of future environmental changes due to nuclear accidents or activities, both domestically and internationally.

Studies on diurnal variation of atmospheric tritium concentration at a sampling location near to PHWR site in Semi-Arid Zone, India.

Tritium (3H) is one of the important long-lived radioisotopes in the gaseous effluent released from Pressurised Heavy Water Reactors (PHWR). For the first time, the studies on diurnal variation of atmospheric tritium concentration was carried out using an in-house developed automatic air moisture collection sampler at Kakrapar Gujarat site, India, where PHWRs are operational. Correlation of diurnal variation of atmospheric tritium concentration with meteorological parameters such as absolute humidity, ambient temperature and wind speed is studied and presented in this paper. Positive and significant correlation of atmospheric 3H concentration was observed with respect to the absolute humidity. Negative correlation was observed in ambient temperature and wind speed. The diurnal maximum and minimum of 3H concentration was found during 21.00-23.00 h (night) and 13.00-16.00 h (day), respectively.

Flux of tritium from the sea to the atmosphere around a nuclear reprocessing plant: Experimental measurements and modelling for the Western English channel.

Tritium is released to the environment by nuclear industries in various forms, mainly HTO. In impact studies leading to estimated doses for the population, atmospheric discharges are mainly taken into consideration because they generally lead to values higher than those related to liquid discharges. However, the tritium released in liquid environments can be transferred to the atmosphere by evaporation and then be transported to terrestrial ecosystems by wind. This study was carried out in France near a fuel reprocessing plant (RP) which discharges tritium into the western English Channel. We highlighted the influence of a mass of water enriched with tritium on the HTO levels in atmospheric water vapour downwind through 18 field campaigns. A hydrodynamic model able to simulate tritium activity in the water was coupled with an evaporation an atmospheric transport model. It allows to reconstitute variations in atmospheric tritium on the coast, depending on liquid discharges of tritium from the reprocessing plant. On this basis, when seawater containing 20-100 Bq.L-1 of tritium flows between 0 and 10 km off the coast, variations in atmospheric activity onshore can increase of 2-15 Bq.L-1. Mean tritium quantities released by the sea into the atmosphere in the Western English Channel reached 130 TBq.y-1 over the 2017-2020 period. Emissions were estimated at 0.9-11.3 GBq km-2.y-1 and depends principally on the distance from the liquid discharge point. If we compare the "marine" source term, in HTO form, with the direct source term for gaseous discharges, the marine source term is one order of magnitude greater for the marine region affected by liquid discharges. Finally, we estimate that approximately 1.1% of tritium stock discharged at sea (regulated and controlled) return to the atmosphere each year at the scale of the Western English Channel.

Tritium and radiocarbon in the water column of the Red Sea.

Despite being the busiest transient sea in the world due to the Suez Canal, radionuclide distribution studies in seawater and sediment of the Red Sea remain rare. A sampling expedition in the Red Sea was conducted from June 9 to July 6, 2021, visiting a transect of several deep sampling stations located along the central axis of the basin from the Gulf of Aqaba to the southern Red Sea (near Farasan Island, Saudi Arabia). The collected seawater profile samples were analyzed for tritium, radiocarbon and oxygen-18. The observed tritium levels in surface waters of the Red Sea peaked at 0.3-0.4 TU, similar to the values observed in the western Arabian Sea (decay corrected). The values observed at waters below 150 m were around 0.2 TU, however, at depths of 450 and 750 m, tritium minima (<0.2 TU) were observed, which could be associated with a partial return flow of bottom waters from the southern to the northern Red Sea. At two stations at the depth of about 550 m, deep Δ14C minima were observed as well (-4‰ and -10‰), documenting ongoing transport of carbon in the water column, important for sink of anthropogenic carbon.

Changes in the Structure of Potato Virus A Virions after Limited in situ Proteolysis According to Tritium Labeling Data and Computer Simulation.

Coat proteins (CP) of the potato virus A virions (PVA) contain partially disordered N-terminal domains, which are necessary for performing vital functions of the virus. Comparative analysis of the structures of coat proteins (CPs) in the intact PVA virions and in the virus particles lacking N-terminal 32 amino acids (PVAΔ32) was carried out in this work based on the tritium planigraphy data. Using atomic-resolution structure of the potato virus Y potyvirus (PVY) protein, which is a homolog of the CP PVA, the available CP surfaces in the PVY virion were calculated and the areas of intersubunit/interhelix contacts were determined. For this purpose, the approach of Lee and Richards [Lee, B., and Richards, F. M. (1971) J. Mol. Biol., 55, 379-400] was used. Comparison of incorporation profiles of the tritium label in the intact and trypsin-degraded PVAΔ32 revealed position of the ΔN-peptide shielding the surface domain (a.a. 66-73, 141-146) and the interhelix zone (a.a. 161-175) of the PVA CP. Presence of the channels/cavities was found in the virion, which turned out to be partially permeable to tritium atoms. Upon removal of the ΔN-peptide, decrease in the label incorporation within the virion (a.a. 184-200) was also observed, indicating possible structural transition leading to the virion compactization. Based on the obtained data, we can conclude that part of the surface ΔN-peptide is inserted between the coils of the virion helix thus increasing the helix pitch and providing greater flexibility of the virion, which is important for intercellular transport of the viruses in the plants.

Primary standardization of 212Pb activity by liquid scintillation counting.

An activity standard for 212Pb in equilibrium with its progeny was realized, based on triple-to-double coincidence ratio (TDCR) liquid scintillation (LS) counting. A Monte Carlo-based approach to estimating uncertainties due to nuclear decay data (branching ratios, beta endpoint energies, γ-ray energies, and conversion coefficients for 212Pb and 208Tl) led to combined standard uncertainties ≤ 0.20 %. Confirmatory primary measurements were made by LS efficiency tracing with tritium and 4παß(LS)-γ(NaI(Tl)) anticoincidence counting. The standard is discussed in relation to current approaches to 212Pb activity calibration. In particular, potential biases encountered when using inappropriate radionuclide calibrator settings are discussed.

The impact of tritium phytoremediation on plant health as measured by fluorescence.

Phytoremediation, using plants for soil, sediment, or water contaminant clean-up, is an established technology dependent on plant health. Tritium (3H), a radioactive isotope of hydrogen that is generally found in the environment as tritiated water (HTO), is a low-level beta emitter with a half-life of 12.32 years. Chlorophyll fluorescence (CF) for monitoring risk assessment of tritium to plant health was conducted at the Tritium Irrigation Facility (TIF) located on the US Department of Energy's Savannah River Site (SRS) near Aiken, SC. Two fluorometers were evaluated in conjunction with phytoremediation at the 25 -acre TIF where tritiated groundwater is being spray-irrigated on a mixed coniferous/deciduous forested watershed as a means of reducing tritium release to a nearby stream that serves as a tributary to the Savannah River. Tritium activity in irrigated water averaged 104 + 42 pCi mL-1 during the 2003 project. Fluorescence parameters measured by the two fluorometers were well correlated with each other (p < 0.0001). Tritium in water respired from oak leaves ranged up to 1845.13 pCi ml-1 and 2138.22 pCi ml-1 in pine needles. Trees in both the test and control sites were approximately 15 years old. Here we demonstrated that fluorescence parameters provide an effective way to estimate the impact of HTO on plant health in a noninvasive, extremely rapid, and cost-effective manner. In the current study applying fluorometry, plants within the TIF phytoremediation site exposed to the site tritiated water were not significantly impacted by the tritium phytoremediation based on CF parameters as compared to the control, a nascent non-irrigated site.

Development and calibration of a modifiable passive sampler for monitoring atmospheric tritiated water vapor in different environments.

Anthropogenic release of tritium from nuclear facilities is expected to increase significantly in the coming decades, which may cause radiation exposure to humans through the contamination of water and food chains. It is necessary and urgent to acquire detailed information about tritium in various environments for studying its behavior and assessing the potential radiation risk. In the atmosphere, although the passive sampling technique provides a low-cost and convenient way to characterize the dynamics of tritiated water vapor (HTO), a single, simple sampler configuration makes it difficult to collect sufficient and representative samples within the expected period from different environments. In this study, we systematically studied the impacts of sampler configurations on sampling performance and proposed a modifiable sampler design by scaling sampler geometry and adjusting absorbent to achieve different monitoring demands. The samplers were subsequently deployed at five sites in China and Germany for the field calibration and the measured results exhibited a good agreement between the adsorption process obtained in sites corrected with diffusion coefficient and the one calibrated in Shanghai. This suggests the feasibility of predicting sampling performance in the field based on known data. Finally, we developed a strategy for sampler modification and selection in different environments and demonstrated that using easily obtainable environmental data, our sampler can be optimized for any area without any time-consuming preliminary experiments. This work provides a scientific basis for establishing high-resolution atmospheric HTO database and expands the conventional empirical sampler design paradigm by demonstrating the feasibility of using quantitative indices for sampler performance customization.

TRITIUM IN THE ENVIRONMENT.

Environmental tritium are natural and anthropogenic origins, the distribution has spread in atmosphere, hydrosphere and biosphere as a variety of chemical forms. The natural tritium is produced by nuclear reactions of neutron with N and O in the upper atmosphere, the production rate changes with 11-year cycle of the solar activity. The production and radioactive decay of natural tritium is balanced on the whole earth, results in the inventory of about 1 EBq. Anthropogenic tritium by nuclear weapons testing had been released in 1950s-1960s, at highest intensity just before the Partial Test Ban Treaty in 1963, and the total release would be 186 EBq. In accordance with a peaceful use of nuclear energy, tritium has been releasing to the environment as airborne and liquid effluents from nuclear power plants and nuclear fuel reprocessing plants. The release from the nuclear power plants depends on the reactor type. Other sources are the tritium production facility of military purpose and the consumer products that use tritium as luminescent energy and disposed to landfill site. Internal dose is only concerned on tritium due to low decay energy, suggesting tritium concentrations in drinking water and food are critical for dose evaluation.