Radionuclide concentrations in the diet of residents in a high level natural radiation area in Iran

Concentrations of ¹³⁷Cs and ²²⁶Ra in the diet (foodstuffs and drinking water) of adult inhabitants in the high-level natural radiation area (HLNRA) of Ramsar, Iran have been determined. The annual intake of foodstuffs was estimated on the basis of their average annual consumption. Food samples collected from local markets were analyzed by means of a gamma spectrometer. The estimated annual dietary intakes of ¹³⁷Cs and ²²⁶Ra were 130Bq and 245Bq, respectively. The concentrations of natural radionuclides in food and drinking water of the residents are higher than the world average, and are correlated with the high concentration of these radionuclides in soil and water. Calculations were also made to determine the potential dose to an individual consuming such diets.     

Removal Efficiency of Radioactive Cesium and Iodine Ions by a Flow-Type Apparatus Designed for Electrochemically Reduced Water Production

The Fukushima Daiichi Nuclear Power Plant accident on March 11, 2011 attracted people’s attention, with anxiety over possible radiation hazards. Immediate and long-term concerns are around protection from external and internal exposure by the liberated radionuclides. In particular, residents living in the affected regions are most concerned about ingesting contaminated foodstuffs, including drinking water. Efficient removal of radionuclides from rainwater and drinking water has been reported using several pot-type filtration devices. A currently used flow-type test apparatus is expected to simultaneously provide radionuclide elimination prior to ingestion and protection from internal exposure by accidental ingestion of radionuclides through the use of a micro-carbon carboxymethyl cartridge unit and an electrochemically reduced water production unit, respectively. However, the removability of radionuclides from contaminated tap water has not been tested to date. Thus, the current research was undertaken to assess the capability of the apparatus to remove radionuclides from artificially contaminated tap water. The results presented here demonstrate that the apparatus can reduce radioactivity levels to below the detection limit in applied tap water containing either 300 Bq/kg of ¹³⁷Cs or 150 Bq/kg of ¹²⁵I. The apparatus had a removal efficiency of over 90% for all concentration ranges of radio–cesium and –iodine tested. The results showing efficient radionuclide removability, together with previous studies on molecular hydrogen and platinum nanoparticles as reactive oxygen species scavengers, strongly suggest that the test apparatus has the potential to offer maximum safety against radionuclide-contaminated foodstuffs, including drinking water.     

Radiation exposure from radionuclides in ground water: an uncertainty analysis for selected exposure scenarios

The uncertainty of the potential radiation exposure of the general population has been estimated for a normalized contamination of ground water that is being used as drinking water for humans and animals, for irrigation of food and feed crops, and for fish production in freshwater bodies. The frequency distributions of annual effective dose equivalents were calculated assuming a normalized activity concentration in water of 1 Bq/l for each radionuclide considered. Estimated frequency distributions of the parameters were used as model input. This estimation is based on an exposure scenario which reflects the present radioecological conditions. Another important source for the uncertainty of the potential dose due to radionuclides released to the ground water is the uncertainty of the exposure scenario. Since such a contamination may not occur before some time in the far future, it is impossible to predict the exact boundary conditions. Therefore, scenarios were simulated with modified consumption habits, more extensive farm management and different climatic conditions. The distributions of the potential doses cover in general about a factor of 10–20. The intake of drinking water, the root uptake and the contamination of fish are most important for the resulting potential radiation exposure. For nearly all radionuclides, the intake of drinking water dominates the potential exposure. In most cases radioactive daughter nuclides are of minor importance. In general, the influence of the exposure scenario on the dose is relatively small. Received: 21 December 1995 / Accepted in revised form: 3 June 1996     

Dietary and physiological controls on the hydrogen and oxygen isotope ratios of hair from mid‐20th century indigenous populations

A semimechanistic model has recently been proposed to explain observed correlations between the H and O isotopic composition of hair from modern residents of the USA and the isotopic composition of drinking water, but the applicability of this model to hair from non‐USA and preglobalization populations is unknown. Here we test the model against data from hair samples collected during the 1930s–1950s from populations of five continents. Although C and N isotopes confirm that the samples represent a much larger range of dietary “space” than the modern USA residents, the model is able to reproduce the observed δ²H and δ¹⁸O values given reasonable adjustments to 2 model parameters: the fraction of dietary intake derived from locally produced foods and the fraction of keratin H fixed during the in vivo synthesis of amino acids. The model is most sensitive to the local dietary intake, which appears to constitute between 60% and 80% of diet among the groups sampled. The isotopic data are consistent with a trophic‐level effect on protein H isotopes, which we suggest primarily reflects mixing of ²H‐enriched water and ²H‐depleted food H in the body rather than fractionation during biosynthesis. Samples from Inuit groups suggest that humans with marine‐dominated diets can be identified on the basis of coupled δ²H and δ¹⁸O values of hair. These results indicate a dual role for H and O isotopic measurements of keratin, including both biological (diet, physiology) and environmental (geographic movement, paleoclimate) reconstruction. Am J Phys Anthropol, 2009. © 2009 Wiley‐Liss, Inc.     

Reconstruction of the contamination of the Techa River in 1949–1951 as a result of releases from the “MAYAK” Production Association

More accurate reconstruction of the radioactive contamination of the Techa River system in 1949–1951 has been made on the basis of refined data on the amounts and the rate of discharge of radionuclides into the Techa River from the Mayak Production Association; this has led to the development of a modified Techa River model that describes the transport of radionuclides through the up-river ponds and along the Techa River and deposition of radionuclides in the river-bottom sediments and flooded areas. The refined Techa River source-term data define more precisely the time-dependent rates of release and radionuclide composition of the releases that occurred during 1949–1951. The Techa River model takes into account the time-dependent characteristics of the releases and considers (a) the transport of radionuclides adsorbed on solid particles originally contained in the discharges or originating in the up-river ponds as a result of stirring up of contaminated bottom sediments and (b) the transport of radionuclides in soluble form. The output of the Techa River model provides concentrations of all source-term radionuclides in the river water, bottom sediments, and floodplain soils at different distances from the site of radioactive releases for the period of major contamination in 1950–1951. The outputs of the model show good agreement with historical measurements of water and sediment contamination. In addition, the river-model output for ⁹⁰Sr concentration in the river water is harmonized with retrospective estimates derived from the measurements of ⁹⁰Sr in the residents of the Techa Riverside villages. Modeled contamination of the floodplain soils by ¹³⁷Cs is shown to be in agreement with the values reconstructed from late measurements of this radionuclide. Reconstructed estimates of the Techa River contamination are being used for the quantification of internal and external doses received by residents of the Techa Riverside communities.     

Reconstruction of radionuclide intakes for the residents of East Urals Radioactive Trace (1957–2011)

The East Urals Radioactive Trace (EURT) was formed after a chemical explosion in the radioactive waste-storage facility of the Mayak Production Association in 1957 (Southern Urals, Russia) and resulted in an activity dispersion of 7.4?×?10¹⁶ Bq into the atmosphere. Internal exposure due to ingestion of radionuclides with local foodstuffs was the main factor of public exposure at the EURT. The EURT cohort, combining residents of most contaminated settlements, was formed for epidemiological study at the Urals Research Center for Radiation Medicine, Russia (URCRM). For the purpose of improvement of radionuclide intake estimates for cohort members, the following data sets collected in URCRM were used: (1) Total β-activity and radiochemical measurements of ⁹⁰Sr in local foodstuffs over all of the period of interest (1958–2011; n?=?2200), which were used for relative ⁹⁰Sr intake estimations. (2) ⁹⁰Sr measurements in human bones and whole body (n?=?338); these data were used for average ⁹⁰Sr intake derivations using an age- and gender-dependent Sr-biokinetic model. Non-strontium radionuclide intakes were evaluated on the basis of ⁹⁰Sr intake data and the radionuclide composition of contaminated foodstuffs. Validation of radionuclide intakes during the first years after the accident was first carried out using measurements of the feces β-activity of EURT residents (n?=?148). The comparison of experimental and reconstructed values of feces β-activity shows good agreement. ⁹⁰Sr intakes for residents of settlements evacuated 7–14 days after the accident were also obtained from ⁹⁰Sr measurements in human bone and whole body. The results of radionuclide intake reconstruction will be used to estimate the internal doses for the members of the EURT cohort.     

Considerations on the behavior of long-lived radionuclides in the soil

The migration of radionuclides from waste repositories to the biosphere potentially leads to a contamination of soil. Due to the importance of food production, the mobilisation and accumulation behaviour of long-lived radionuclides in the soil plays a key role in performance assessment studies. In this paper, the main features and processes that control radionuclide behaviour in soil, such as pH, redox potential and sorption to organic and inorganic soil components, are discussed for the radionuclides ³⁶Cl, ⁷⁹Se, ¹²⁹I, ⁹⁹Tc, ²³⁷Np and ²³⁸U, that are usually most relevant in long-term safety assessments of nuclear waste. The interaction of radionuclide behaviour in soil with environmental factors, such as temperature and humidity as well as farming practices are discussed. The possible impact of future soil development on long-term behaviour in soil are taken into consideration. Due to the physiological constraints of plant growth, appropriate soil conditions for growth will probably not be substantially different from current requirements, bearing in mind that sustainable agriculture strives for optimal plant growth. Against this background, present-day parameters may in general be considered appropriate for roughly estimating the behaviour of radionuclides in the soil-plant system. Received: 18 October 2000 / Accepted: 20 March 2001     

Pilot study of the Urals population by tooth electron paramagnetic resonance dosimetry

During 1949–1956, about 76 × 10⁶ m³ of radioactive liquid waste containing a total activity of 10¹⁷ Bq was discharged into the Techa River by the first Russian industrial nuclear facility Mayak. As a consequence, the population living in the river valley received considerable internal and external radiation doses. The results of a first application of electron paramagnetic resonance (EPR) of tooth enamel for a retrospective individual dose evaluation of the residents of the Techa riverside are presented. Three main contributions to the dose absorbed in tooth enamel have been considered: external exposure mainly from the Techa River sediments, internal exposure mainly due to ⁹⁰Sr; and background radiation including all other sources of exposure except the Techa River. The teeth of 86 inhabitants of the town Kamensk-Uralskii were analysed to determine the age-dependent contribution of the background radiation to the enamel dose. For 22 residents of the middle and lower Techa riverside, measurements of the ⁹⁰Sr whole-body content and EPR measurements of the absorbed dose in enamel were used to establish a correlation between these two quantities. Finally, absorbed doses in the enamel of five residents of the upper Techa riverside were determined by the EPR method. Contributions of the background radiation and the internal ⁹⁰Sr contamination were subtracted to determine the external exposure of the residents.     

Transfer of radionuclides to ants, mosses and lichens in semi-natural ecosystems

There is a scarcity of data on transfer of both natural and anthropogenic radionuclides to detritivorous invertebrates for use in the assessment of radiation exposure. Although mosses and lichens have been extensively used in biomonitoring programs, the data on transfer of radionuclides to these species are limited, particularly for natural radionuclides. To enhance the available data, activity concentrations of ¹³⁷Cs, ²²⁶Ra and ²²⁸Ra were measured in ants, mosses and lichens and corresponding undisturbed soil collected from semi-natural ecosystems in Serbia and Montenegro and biota/soil concentration ratios (CR) calculated. Since the majority of internal dose to biota is expected to come from ⁴⁰K, the activity concentrations of this radionuclide were also determined. The mean CR values for ¹³⁷Cs, ²²⁶Ra and ²²⁸Ra in ants analyzed in this study were found to be 0.02, 0.06 and 0.02, respectively. The mean CR values of radionuclides in mosses were found to be 2.84 for ¹³⁷Cs, 0.19 for ²²⁶Ra and 0.16 for ²²⁸Ra, while those in lichens were found to be 1.08 for ¹³⁷Cs, 0.15 for ²²⁶Ra and 0.13 for ²²⁸Ra. The CR values obtained in this study were compared with default CR values used in the ERICA Tool database and also with those reported in other studies.     

Sedimentation and distribution of gamma-emitting radionuclides in bottom sediments of southern Lake Päijänne,Finland, after the Chernobyl accident

The rates of sedimentation of fallout nuclides were determined by means of sediment traps during 28 months after the Chernobyl accident in southern Lake Päijänne, Finland. The spatial distribution of the radionuclide content of the lake bottom was studied on 35 sediment cores in winters 1987/88 and 1988/89. The results were compared with simultaneous observations of the radionuclide content of the water and seston. The role of different transfer mechanisms in the elimination of radionuclides from the water column is discussed.The values recorded for the flux to the lake sediments were on average of the same order of magnitude as the initial deposition on the lake surface (Cs-137 65 kBqm^–2). The radionuclide flux to the sediments was rapid during the first months after the accident. After that the elimination of dissolved nuclides from the water mass became significantly slower. The highest flux rate was that of Ce-144 and the lowest that of Rh-106 (Ru-106). Of the radiocesium, about half of the initial inventory was transferred to the sediments after the first observation year.The content of radionuclides showed considerable spatial variation on the lake bottom (Cs-137 7–280 kBqm^–2). Direct adsorption of radiocesium explains unexpectedly high concentrations on shallow erosion bottoms. There was a clear tendency for the concentrations to increase with depth, as a result of the focusing effect. Sediment resuspension had a significant impact on the total flux of radionuclides to deepwater sediments. Estimates were made of the resuspended flux of radionuclides.     

Genotoxicity and toxicity assay of water sampled from the underground nuclear explosion site in the north of the Perm region (Russia)

The results of our study revealed a local biologically relevant surface water contamination in the radionuclide anomaly in the north of Russia (Perm region) by means of Allium shoenoprasum L. the anaphase-telophase chromosome aberration assay. This radionuclide anomaly was formed in 1971 as a result of an underground nuclear explosion with soil excavation. Specific activities of main dose-forming radionuclides in all examined reservoirs are below intervention levels officially adopted in Russia for drinking water. We found that 90Sr significantly contribute to induction of cytogenetic disturbances. Our previous and described here data suggest that metal ions and radionuclides combined exposure on the various biota species (with the dose below permissible exposure limits for human) may cause substantial biological effects in part be due to synergic response. The findings described here indicated that development of a new concept of radiation protection for humans and biota should be based on the clear understanding of biological effects of low doses of radiation in chronic exposure to multi-pollutant mixtures.     

Natural variation in <Superscript>210</Superscript>Po and <Superscript>210</Superscript>Pb activity concentrations in the urine of Finnish population groups

A study to determine activity concentrations of ²¹⁰Pb and ²¹⁰Po in the urine of certain Finnish population groups was conducted, to investigate the variation in natural background level of urinary excretion. The study participants were divided into three groups mainly based on their diet. The first group comprised recreational fishermen and the second group represented people consuming more reindeer meat than an average Finn, while people using drinking water with very high activity concentrations of ²¹⁰Po were selected for the third group. The fourth group was a control group. The mean urinary excretion of ²¹⁰Po in groups 1 and 2 was 73 and 100 mBq d⁻¹, respectively. These values were higher than the value of the control group (20 mBq d⁻¹) and the mean values reported in the literature. The mean daily urinary excretion of ²¹⁰Pb in groups 1 and 2, 70 and 52 mBq d⁻¹, was also slightly higher than that in the control group (32 mBq d⁻¹). In contrast, the excretion rates of both ²¹⁰Po and ²¹⁰Pb for the members of group 3 were one to two orders of magnitude higher than those reported in the literature. This was clearly due to the elevated levels of natural radionuclides in their drinking water. The present study demonstrates the importance of possessing good knowledge of the background levels, in order to allow the determination of the additional exposure due, for example, to the malevolent use of radiation.     

Activity concentrations of <Superscript>226</Superscript>Ra, <Superscript>228</Superscript>Th,and <Superscript>40</Superscript>K in different food crops from a high background radiation area in Bitsichi,Jos Plateau,Nigeria

One of the three goals of the United Nations for sustainable food security is to ensure that all people have access to sufficient, nutritionally adequate, and safe food. Decades of tin mining in the Bitsichi area of the Jos Plateau, Nigeria, have left a legacy of polluted water supplies, impoverished agricultural land, and soil containing abnormally high levels of naturally occurring radioactive elements. In order to ascertain the radiological food safety of the population, different crops that constitute the major food nutritive requirements were collected directly across farmlands in the area. The activity concentrations of ²²⁶Ra, ²²⁸Th, and ⁴⁰K were determined in the food and soil samples using γ-ray spectrometry. Additionally, in situ gamma dose rate measurements were performed on the farms using a pre-calibrated survey meter. The corresponding activity concentrations in the food crops ranged from below detection limit (BDL) to 684.5 Bq kg⁻¹ for ⁴⁰K, from BDL to 83.5 Bq kg⁻¹ for ²²⁶Ra, and from BDL to 89.8 Bq kg⁻¹ for ²²⁸Th. Activity concentrations of these radionuclides were found to be lower in cereals than in tubers and vegetables. As for the soil samples, activity concentrations of these radionuclides varied from BDL to 166.4 Bq kg⁻¹, from 10.9 to 470.6 Bq kg⁻¹, and from 122.7 to 2,189.5 Bq kg⁻¹ for ⁴⁰K, ²²⁶Ra, and ²²⁸Th, respectively. Average external gamma dose rates were found to vary across the farms from 0.50 ± 0.01 to 1.47 ± 0.04 μSv h⁻¹. Due to past mining activities, the soil radioactivity in the area has been modified and the concentration level of the investigated natural radionuclides in the food crops has also been enhanced. However, the values obtained suggest that the dose from intake of these radionuclides by the food crops is low and that harmful health effects are not expected.     

Dose assessment for the Metlino and Muslyumovo populations who lived along the Techa river from 1949 to 1954

In the period from 1949 to 1956, liquid radioactive waste was routinely and accidentally discharged by the Mayak Production Association, Southern Urals, Russia, into the Techa river. Based on a novel approach, the contamination of the Techa river water, the bottom sediments and the adjacent flood plains was modelled, and internal and external doses were estimated for two villages located downstream of the site of liquid radioactive waste release. Altogether, 11 radionuclides that occurred in the liquid radioactive waste were included in the calculations. The results suggest significantly higher doses than previously assumed, with the major contribution in the year 1951. Radionuclides with half-lives of less than 1 year, such as ⁸⁹Sr, ¹³¹I, ⁹⁵Zr+⁹⁵Nb, ¹⁰³Ru+^103mRh, ¹⁴⁰Ba+¹⁴⁰La, and ¹⁴⁴Ce+¹⁴⁴Pr, represent the major sources and, in contrast, long-lived radionuclides, such as ⁹⁰Sr and ¹³⁷Cs that have so far been assumed to be most important, did not dominate the doses. For adults from the village Metlino, located 7 km downstream of the site of liquid radioactive waste discharge, the committed effective doses due to intake of radionuclides were calculated to be about 2.3 Sv, while the external doses were between about 1.2 Sv and 6.9 Sv. On the other hand, for adults from Muslyumovo, located 75 km downstream, the commited effective doses due to intake of radionuclides were calculated to be about 0.5 Sv, while the external doses were between 0.5 Sv and 2.0 Sv. The values for the skin doses to the Metlino and Muslyumovo populations were about 7.1 Sv and 1.3 Sv, respectively. It is concluded that the current dose estimates for the residents of the Techa river need, therefore, reevaluation.     

Radionuclides and Radiation Indices of High Background Radiation Area in Chavara-Neendakara Placer Deposits (Kerala,India)

The present paper describes a detailed study on the distribution of radionuclides along Chavara – Neendakara placer deposit, a high background radiation area (HBRA) along the Southwest coast of India (Kerala). Judged from our studies using HPGe gamma spectrometric detector, it becomes evident that Uranium (²³⁸U), Thorium (²³²Th) and Potassium (⁴⁰K) are the major sources for radioactivity prevailing in the area. Our statistical analyses reveal the existence of a high positive correlation between ²³⁸U and ²³²Th, implicating that the levels of these elements are interdependent. Our SEM-EDAX analyses reveal that titanium (Ti) and zircon (Zr) are the major trace elements in the sand samples, followed by aluminum, copper, iron, ruthenium, magnesium, calcium, sulphur and lead. This is first of its kind report on the radiation hazard indices on this placer deposit. The average absorbed dose rates (9795 nGy h⁻¹) computed from the present study is comparable with the top-ranking HBRAs in the world, thus offering the Chavara-Neendakara placer the second position, after Brazil; pertinently, this value is much higher than the World average. The perceptibly high absorbed gamma dose rates, entrained with the high annual external effective dose rates (AEED) and average annual gonadal dose equivalent (AGDE) values existing in this HBRA, encourage us to suggest for a candid assessment of the impact of the background radiation, if any, on the organisms that inhabit along this placer deposit. Future research could effectively address the issue of the possible impact of natural radiation on the biota inhabiting this HBRA.     

Investigation of the radiation risk due to environmental contamination by <Superscript>241</Superscript>Am from lightning rods disposed at uncontrolled garbage dumps

Radioactive lightning rods were manufactured in Brazil until 1989, when the licenses for using radioactive sources in these products were lifted by the national nuclear authority. Since then, these rods have been replaced by the Franklin type and collected as radioactive waste. However, only 20% of the estimated total number of installed rods has been delivered to the Brazilian Nuclear Commission. This situation causes concern, since there is the possibility of the rods to be disposed as domestic waste. In Brazil, 64% of the municipal solid waste is disposed at garbage dumps without sufficient control. In addition, ²⁴¹Am, the radionuclide most commonly employed, is classified as a high-toxicity element, when incorporated. In the present study, ²⁴¹Am migration experiments were performed by means of a lysimeter system, in order to evaluate the risk of contamination caused by radioactive lightning rods disposed as common solid waste. ²⁴¹Am sources removed from lightning rods were placed inside lysimeters filled with organic waste that was collected at the restaurant of the Instituto de Pesquisas Energéticas e Nucleares. The generated leachate was periodically analyzed, and characteristics such as pH, redox potential, solid content and the concentration of the radioactive material were determined. The equivalent dose for members of the public was calculated considering ingestion of contaminated drinking water as the major path of exposure. Estimated doses were about 20-times below the effective dose limit of 1 mSv year⁻¹ for members of the public as recommended by the International Commission on Radiological Protection. This suggests the radiation risk caused by lightning rods disposed at uncontrolled garbage dumps to be low. It should be noted, however, that the number of investigated lightning rods was quite small. The results of this study might therefore not be entirely representative and should be interpreted with care. They provide, however, a very first basis for characterizing the transfer of ²⁴¹Am from lightning rods to the human food chain.     

Estimation of Multimedia Inorganic Arsenic Intake in the U.S. Population

Arsenic is widely distributed in the environment by natural and human means. The potential for adverse health effects from inorganic arsenic depends on the level and route of exposure. To estimate potential health risks of inorganic arsenic, the apportionment of exposure among sources of inorganic arsenic is critical. In this study, daily inorganic arsenic intake of U.S. adults from food, water, and soil ingestion and from airborne particle inhalation was estimated. To account for variations in exposure across the U.S., a Monte Carlo approach was taken using simulations for 100,000 individuals representing the age, gender, and county of residence of the U.S. population based on census data. Our analysis found that food is the greatest source of inorganic arsenic intake and that drinking water is the next highest contributor. Inhalation of airborne arsenic-containing particles and ingestion of arsenic-containing soils were negligible contributors. The exposure is best represented by the ranges of inorganic arsenic intake (at the 10^th and 90^th percentiles), which were 1.8 to 11.4 µg/day for males and 1.3 to 9.4 µg/day for females. Regional differences in inorganic arsenic exposure were due mostly to consumption of drinking water containing differing inorganic arsenic content rather than to food preferences.     

Radionuclides in Surface Waters,Bottom Sediments,and Hydrobionts in the Neman River

The specific/volumetric activity of radionuclides has been determined at global background levels in surface waters, bottom sediments, and hydrobionts at the site of the planned hydrotechnical facilities of the Baltic nuclear power plant (NPP). The presence of Sr⁹⁰ and Cs^l37 in the water medium due to global processes of the formation of radioactivity in the natural environment and the content of ³H have been studied. It is established that the background values of the specific/volumetric activity of radionuclides are significantly lower than the admissible values according to NRB-99/2009, being at the level of the previous years (2009–2014). The results of these studies will serve as a basis for precision instrumental estimates of the effect of the Baltic NPP operation on the environment and will also be used to establish the background values of environmental parameters in the nuclear power site.     

Replacing sweetened caloric beverages with drinking water is associated with lower energy intake

Objective: Reduced intake of sweetened caloric beverages (SCBs) is recommended to lower total energy intake. Replacing SCBs with non‐caloric diet beverages does not automatically lower energy intake, however. Compensatory increases in other food or beverages reportedly negate benefits of diet beverages. The purpose of this study was to evaluate drinking water as an alternative to SCBs. Research Methods and Procedures: Secondary analysis of data from the Stanford A TO Z intervention evaluated change in beverage pattern and total energy intake in 118 overweight women (25 to 50 years) who regularly consumed SCBs (>12 ounces/d) at baseline. At baseline and 2, 6, and 12 months, mean daily beverage intake (SCBs, drinking water, non‐caloric diet beverages, and nutritious caloric beverages), food composition (macronutrient, water, and fiber content), and total energy intake were estimated using three 24‐hour diet recalls. Beverage intake was expressed in relative terms (percentage of beverages). Results: In fixed effects models that controlled for total beverage intake, non‐caloric and nutritious caloric beverage intake (percentage of beverages), food composition, and energy expenditure [metabolic equivalent (MET)], replacing SCBs with drinking water was associated with significant decreases in total energy intake that were sustained over time. The caloric deficit attributable to replacing SCBs with water was not negated by compensatory increases in other food or beverages. Replacing all SCBs with drinking water was associated with a predicted mean decrease in total energy of 200 kcal/d over 12 months. Discussion: The results suggest that replacing SCBs with drinking water can help lower total energy intake in overweight consumers of SCBs motivated to diet.     

Water quality and Human Health Risk Assessment: a case study of the Czarna Przemsza River source in Zawiercie,Poland

Abstract

The water quality of the Czarna Przemsza River source in Zawiercie was investigated in four sampling campaigns in years 2016 and 2017. Values of 62 indicators (physico-chemical, inorganic, organic, and biological) were compared with permissible limits for drinking water according to Polish legal acts and EU, WHO, USEPA, and Canadian guidelines. The water quality was determined as below good because of EC values and As, Ca, Cd, Cr, Cu, Se, and Zn concentrations. Water was also determined as non-potable due to exceeded concentrations of Al, As, Cd, Cr, Fe, K, Ni, Pb, Sb, and Se. The Human Health Risk Assessment for Zawiercie’s inhabitants was carried out, while water from the source is consumed regardless of its quality. The mean estimated daily intake (EDI) values exceeded Minimal Risk Level values forCr, Cd, As, Se, and Cu. The hazard index (HI) values pointed very high total non-carcinogenic risk in residential exposure scenario generated mainly by As, Cr(VI), Tl, Pb, MCPA, Se, and Cd. Water intake scenario based on questionnaire surveys pointed that risk for inhabitants existed (HI >1). The total carcinogenic risk (R_t) values were at the unacceptable level and decreased in the following order: Cr(VI) > As?>?Pb.