Microbial extracellular enzyme activities in Humex Lake Skjervatjern

Two microbial extracellular enzyme activities (MEEA) were studied in HUMEX Lake Skjervatjern: acid phosphatase (APHA) and leucine aminopeptidase (LeuAMPA). Both enzyme activities varied in the vertical and horizontal scale in both lake sites. APHA varied in the acidfied Basin A between 945–1706 nmol L⁻¹ h⁻¹ and LeuAMPA between 3.7–25 nmol L⁻¹ h⁻¹. Both MEEA reached maxima in 0.5 m depth. In the control site (Basin B), APHA was lower by a factor of two, and varied between 156–669 nmol L⁻¹ h⁻¹. LeuAMPA reached similar values as in Basin A and varied between 7.8–34.8 nmol L⁻¹ h⁻¹. Maxima of APHA were found in the upper layer (0–2 m), while LeuAMPA had only one distinct maxima at 2–2.5 m depth. The number of bacteria (AFDC) varied between 4.4–8.8 10⁶ cells mL⁻¹ and was not significantly different in either side, but both had maxima in the thermocline. Highest specific LeuAMPA activities were found in the thermocline (3.2–4.5 fmol L⁻¹ h⁻¹ cell⁻¹) in both sides and varied between 0.4–4.5 fmol L⁻¹ h⁻¹ cell⁻¹ in both water columns. The main contributor (60–70%) to LeuAMPA was found in the microplankton fraction, retained on Nuclepore filters with pore sizes between 2.0-0.2 μm. APHA was retained less even on a filter with pore size smaller than 0.2 μm. About 50–70% of APHA passed through 0.2 μm-0.1 μm Nuclepore filters and could be found in the dissolved organic matter (DOM) fraction. APHA and bacteria counts (AFDC) showed a distinct gradient from the littoral zone to the pelagial in the surface water samples (0.2 m depth). APHA and LeuAMPA are regarded as important regulators for nutrient availability to microplankton. However, all data from vertical as important regulators for nutrient availability to microplankton. However, all data from vertical and horizontal samples showed that Lake Skjervatjern is a strongly gradient-dominated aquatic ecosystem. Watershed-littoral effects are more pronounced in the shallow, acidified Basin A than in the control side, Basin B.     

Modelling of water-ozone reaction system

Mass transfer and reaction kinetics of raw Nile water ozonation are examined. The contact system is a perfectly mixed reactor, and ozone is bubbled through a glass diffuser at different supply rates. The ozone residual is detected for different reaction time intervals. A simple mathematical model is proposed to describe the mechanism of the ozone reactions in the reactor. The proposed model quite accurately describes the mass transfer behaviour in the reactor and determines the ozone dissociation rate constant, together with the effect of the chemical reaction on the ozone transfer. A linear relationship is observed between the ozone feed rate and the ozone residual. First order reaction kinetics describes fairly well the autodecomposition and the global reaction rates of ozone in raw water. The mass transfer coefficient is about 0.18 min⁻¹. The dissociation and the reaction rate constants are evaluated to be 0.33 mg L⁻¹ and 0.19 mg L⁻¹min⁻¹.     

Mineral content of drinking water in lowland papua

This study presents concentration of nine minerals (Na, K, Mg, Ca, Cl, Mn, Zn, Cd, Pb) in 31 drinking water samples collected in the Papua New Guinea lowland, where coastal villagers draw water from artificial wells blended with sea water, riverside villagers utilize brackish river water, and inland villagers fetch creek or swamp water whose chemical composition is close to rain water. During the dry season, the coastal well water contains 500 mgL⁻¹ of sodium and 50–90 μgL⁻¹ of lead. The inland creek or swamp water contains very small amount of minerals; on the average, for instance, 0.64 mgL⁻¹ of magnesium, 0.84 mgL⁻¹ of calcium, and 4.78 mgL⁻¹ of water hardness (as CaCO₃). From some epidemiological evidence in industrialized countries, these mineral concentrations are judged to be indicative of high risk of cardiovascular disorders.     

Environmental monitoring using surface water, river sediments, and vegetation: A case study in the Famatina Range, La Rioja, NW Argentina

This work discusses trace elements studied beneath the semiarid endorheic region of the Famatina Range (La Rioja, NW Argentina). The results obtained in 27 control sites allow the determination of five distinct geochemical patterns in the Famatina Range. Pattern 1 reflects the composition of underlying Paleozoic and Tertiary bedrock (background level: water pH, 7.5–9; specific conductance, 0.2–0.7 mS cm⁻¹), which is influenced by mineralization. Pattern 2 exhibits water pH, 6; specific conductance, 0.7 mS cm⁻¹; high contents of Cu, Cd, Rb, Zn, Sn, and Be in waters; and high contents of Cu, Cd, Zn, Pb, Cr, Sb, Ag, Be, Co, Ni, Bi, Rare Earth Elements (REE), Li, Ba, Cs, and Sr in sediments. Pattern 3 exhibits water pH, 3–4; specific conductance, 1.0 mS cm⁻¹; high contents of Pb, Co, Be, Au, As, Cr, Hg, Th, Ba, Cs, Rb, Sb, Y, Zr, REE, and Hf in waters; high contents of Cd, Zn, Mo, and As in sediments). Pattern 3 is also modified by the input of elements from a source external to the Famatina Range. Pattern 4 exhibits water pH, 7–8; specific conductance, 1.5–2.3 mS cm⁻¹; high contents of B, Li, Ba, Sr, and Zn in waters; high contents of Li, Cr, Sr, Ni, and Cs in sediments. Finally, Pattern 5 is developed on the red sandstones from De la Cuesta Formation (water pH, 8; specific conductance, 2.5–5.0 mS cm⁻¹; high contents of Sr, Mo, U, B, Li, Rb, and Hf in waters; high contents of B, Ba, Cs, Li, and Rb in sediments). The mobility of above-mentioned elements is mainly related to water pH changes and evaporation processes.     

Assessment of environmental tobacco smoke and respirable suspended particle exposures for nonsmokers in Hong Kong using personal monitoring

One hundred and ninety-four randomly selected nonsmoking subjects collected air samples in their breathing zone by wearing personal monitors for 24 h. The study was centered in Hong Kong, and comprised housewives in one group, primarily for assessing exposures in the home, and office workers in a second group to assess the contribution of the workplace to overall exposure. Samples collected were analysed for respirable suspended particles (RSP), nicotine, 3-ethenylpyridine, and environmental tobacco smoke (ETS) particles using ultraviolet absorbance (UVPM), fluorescence (FPM), and solanesol measurements (SolPM). Saliva cotinine analyses were also undertaken to confirm the nonsmoking status of the subjects and to investigate their correlation with ETS exposure measurements. Approximately 6% of the subjects in Hong Kong misclassified their nonsmoking status. Median time-weighted average (TWA) RSP concentrations varied from 43 to 54 μg m⁻³ with no significant differences detected between any of the groups investigated. Office workers who lived and worked with smokers were exposed to 2.6 μg m⁻³ ETS particles (SolPM) and 0.44 μg m⁻³ nicotine, based on median TWA concentrations. Median concentrations of ETS particles and nicotine were below the limits of quantification for housewives living with smokers and were not significantly different from those for housewives living with nonsmokers. It would therefore be unreliable in Hong Kong to use a smoking spouse as a marker for assessing health risks related to ETS exposure. The office workers in this study were significantly more exposed to ETS than housewives from either smoking or nonsmoking homes, and the workplace was estimated to contribute over 33% of the annual exposure to ETS particles and nicotine. Exposure estimates suggest that the most highly exposed office workers in this study receive between 11 and 50 cigarette equivalents per year, based upon upper decile levels for ETS particles and nicotine, respectively.     

Mercury in algae of the Canary Islands littoral

The concentrations of Hg in three groups of algae (Phaeophyta, Chlorophyta, and Rhodophyta) found in the Canary Islands littoral were determined. The mean concentrations found were, respectively: Phaeophyta: 0.13 mg kg⁻¹ (range 0.01 to 2.30 mg kg⁻¹); Chlorophyta: 0.13 (range 0.025 to 0.36 mg kg⁻¹); Rhodophyta: 0.11 mg kg⁻¹ (range 0.02 to 0.28 mg kg⁻¹). There are no relevant differences in the contents of Hg at group level and at species level, only a sample of Phaeophyta presents an abnormally high concentration (>1 mg kg⁻¹), corresponding to a sampling station nearby an urban drain.     

Isotope tracing of submarine groundwater discharge offshore Ubatuba, Brazil: results of the IAEA–UNESCO SGD project

Results of groundwater and seawater analyses for radioactive (³H, ²²²Rn, ²²³Ra, ²²⁴Ra, ²²⁶Ra, and ²²⁸Ra) and stable (D and ¹⁸O) isotopes are presented together with in situ spatial mapping and time series ²²²Rn measurements in seawater, direct seepage measurements using manual and automated seepage meters, pore water investigations using different tracers and piezometric techniques, and geoelectric surveys probing the coast. This study represents first time that such a new complex arsenal of radioactive and non-radioactive tracer techniques and geophysical methods have been used for simultaneous submarine groundwater discharge (SGD) investigations. Large fluctuations of SGD fluxes were observed at sites situated only a few meters apart (from 0 cm d⁻¹ to 360 cm d⁻¹; the unit represents cm³/cm²/day), as well as during a few hours (from 0 cm d⁻¹ to 110 cm d⁻¹), strongly depending on the tidal fluctuations. The average SGD flux estimated from continuous ²²²Rn measurements is 17 ± 10 cm d⁻¹. Integrated coastal SGD flux estimated for the Ubatuba coast using radium isotopes is about 7 × 10³ m³ d⁻¹ per km of the coast. The isotopic composition (δD and δ¹⁸O) of submarine waters was characterised by significant variability and heavy isotope enrichment, indicating that the contribution of groundwater in submarine waters varied from a small percentage to 20%. However, this contribution with increasing offshore distance became negligible. Automated seepage meters and time series measurements of ²²²Rn activity concentration showed a negative correlation between the SGD rates and tidal stage. This is likely caused by sea level changes as tidal effects induce variations of hydraulic gradients. The geoelectric probing and piezometric measurements contributed to better understanding of the spatial distribution of different water masses present along the coast. The radium isotope data showed scattered distributions with offshore distance, which imply that seawater in a complex coast with many small bays and islands was influenced by local currents and groundwater/seawater mixing. This has also been confirmed by a relatively short residence time of 1–2 weeks for water within 25 km offshore, as obtained by short-lived radium isotopes. The irregular distribution of SGD seen at Ubatuba is a characteristic of fractured rock aquifers, fed by coastal groundwater and recirculated seawater with small admixtures of groundwater, which is of potential environmental concern and has implications on the management of freshwater resources in the region.     

A quantitative integrated assessment of pollution prevention achieved by Integrated Pollution Prevention Control licensing

This paper presents an innovative, quantitative assessment of pollution avoidance attributable to environmental regulation enforced through integrated licensing, using Ireland's pharmaceutical-manufacturing sector as a case study. Emissions data reported by pharmaceutical installations were aggregated into a pollution trend using an Environmental Emissions Index (EEI) based on Lifecycle Assessment methodologies. Complete sectoral emissions data from 2001 to 2007 were extrapolated back to 1995, based on available data. Production volume data were used to derive a sectoral production index, and determine ‘no-improvement’ emission trends, whilst questionnaire responses from 20 industry representatives were used to quantify the contribution of integrated licensing to emission avoidance relative to these trends. Between 2001 and 2007, there was a 40% absolute reduction in direct pollution from 27 core installations, and 45% pollution avoidance relative to hypothetical ‘no-improvement’ pollution. It was estimated that environmental regulation avoided 20% of ‘no-improvement’ pollution, in addition to 25% avoidance under business-as-usual. For specific emissions, avoidance ranged from 14% and 30 kt a^− 1 for CO₂ to 88% and 598 t a^− 1 for SO_x. Between 1995 and 2007, there was a 59% absolute reduction in direct pollution, and 76% pollution avoidance. Pollution avoidance was dominated by reductions in emissions of VOCs, SO_x and NO_x to air, and emissions of heavy metals to water. Pollution avoidance of 35% was attributed to integrated licensing, ranging from between 8% and 2.9 t a^− 1 for phosphorus emissions to water to 49% and 3143 t a^− 1 for SO_x emissions to air. Environmental regulation enforced through integrated licensing has been the major driver of substantial pollution avoidance achieved by Ireland's pharmaceutical sector — through emission limit values associated with Best Available Techniques, emissions monitoring and reporting requirements, and performance targets specified in environmental management plans. This compliant sector offers a positive, but not necessarily typical, case study of IPPC effectiveness.     

Population exposure to airborne thorium at the high natural radiation areas in India

High natural radiation areas in the coastal and peninsular India were studied for airborne thorium and resultant population exposure due to inhalation. Four locations covering three states viz., Ayiramthengu and Neendakara in Kerala, Kudiraimozhi in Tamil Nadu and Bhimilipatnam in Andhra Pradesh were investigated. External gamma radiation fields 1 m above the monazite ore bodies ranged from 200 to 3000 nGy h^-1. Soil samples showed ²³²Th specific activity varying from 0·1 to 1·5 Bq g^-1 with surface alpha activity in the range of 1·0–12·5 Bq cm^-2. Suspended particulates in the samples ranged from 60–140 μg m^-3 with ²³²Th showing a wider variation of <0·03–0·3 mBq m^-3. There was poor correlation between suspended particulates and long-lived alpha airborne activity . The resuspension factors for ²³²Th were in the range of 1·5×10^-8–7·9×10^-7 cm^-1. Higher resuspension was correlated with dry sand dunes. The upper limits for Committed Effective Dose (CED) due to inhalation of airborne ²³²Th at the respective high natural radiation areas were estimated to range from 50±30 to 300±130 μSv (5–30 mrem) per year per adult member of public assuming an activity median aerodynamic diameter of 1 μm for the airborne particulates.     

Determination of phthalate ester plasticizers in the aquatic environment of Southwestern Nigeria

Water from the Lagos, Oyo, Osun, Ondo, and Delta states of Nigeria and the cities' water treatment plants had been analized for the presence of ubiquitous phthalate esters using liquid chromatography. Extraction with CH₂Cl₂ and liquid chromatography was used for compound separation. Several phthalate esters, dimethyl- (DMP), diethyl- (DEP), and di-n-butyl- (DBP) were found present at levels of 10 mg L⁻¹ to 1472 mg L⁻¹ in river water and 91 mg L⁻¹ to 1219 mg L⁻¹ in tap water from the cities' water treatment plants. A study of uncontaminated water was done to establish blank levels.     

Application of a “closed-can” technique for measuring radon exhalation from mine samples of Punjab, Pakistan

Using the closed-can technique, radon exhalation rate measurements have been carried out for shale and coal samples collected from various mines located in the Chakwal and Makarwal areas of Pakistan. For the two areas, the measured average values of the exhalation rates from shale are 1.45±0.13 and 0.67±0.25 Bq m⁻² h⁻¹ and for coal are 1.0±0.03 and 0.65±0.32 Bq m⁻² h⁻¹, respectively. These values are much lower than the measured exhalation rates from alum-shale-based Nordic concrete which has values in the 50–200 Bq m⁻² h⁻¹ range. The lower values of the measured exhalation rates from the shale and coal deposits in the Chakwal and Makarwal areas are indicative of their lower uranium contents and mine workers in these areas do not face any abnormal health hazard due to radon since the exhalation rates have been found to be on the low side.     

Plutonium isotopes in surface air of Prague in 1986–2006

Monitoring of ^239,240Pu in surface air of Prague started in 1986 in connection with the Chernobyl accident. Measurable activities of 10–28 μBq m⁻³ were found from 29 April 1986 to 5 May 1986. In the most of the monitoring periods of 1987–1996, activities of ^239,240Pu in air were not measurable. Positive values for ^239,240Pu and ²³⁸Pu in air could be obtained after installation of an aerosol sampler with higher flow-rate in 1997. Activity concentrations of ^239,240Pu and ²³⁸Pu in Prague air in the most of quarters of 1997–2006 were in the range 0.53–5.06 and <0.16–1.10 nBq m⁻³, respectively. Seasonal fluctuations can be found in content of ^239,240Pu in air. Activity ratios of ²³⁸Pu/^239,240Pu in air are higher than those in top soil, so it can be supposed that ²³⁸Pu is coming to air of Prague also from other sources than resuspension of fallout from atmospheric nuclear tests.     

Health effects of oxidants

Oxidants of significance to human health include ozone, nitrogen dioxide, and peroxyacetylnitrate. All of these compounds are involved in complex photochemical reactions which makes quantification and prediction of their individual health effects difficult. Ozone causes trauma to lung tissues and interferes with enzyme systems in the lungs and other tissues causing a broad range of symptoms. Measurable health impacts can occur at concentrations as low as 390 μg/m³. Acute effects of ozone exposure are reversible at normal urban concentrations (80–120 μg/m³). A special problem of concern, however, is increased susceptibility to infectious diseases contracted through the lungs. Nitrogen dioxide also causes trauma to lung tissues and interferes with enzyme systems. Measurable impacts can occur at concentrations as low as 100 μg/m³, but recovery is rapid and it is not known whether repeated exposures at this level have cumulative effects or predispose the lungs to permanent damage. Chronic exposure of laboratory animals to higher nitrogen dioxide levels can cause emphysema-like conditions and reduction in resistance to respiratory infection. Epidemiological studies of children in houses with gas stoves confirm the finding of reduced resistance to respiratory infection. The U.S. EPA estimates that health effects may occur in young children exposed to concentrations in excess of 280 to 560 μg/m³ one-hour average. These concentrations occur routinely in houses having gas stoves. Peroxyacetylnitrate is a powerful eye irritant in photochemical smog. Other health effects are similar to those of ozone, but less important because of the relatively low concentrations of this pollutant compared to other oxidants.     

Investigation of volatile organic compounds and phthalates present in the cabin air of used private cars

The presence of selected volatile organic compounds (VOCs) including aromatic, aliphatic compounds and low molecular weight carbonyls, and a target set of phthalates were investigated in the interior of 23 used private cars during the summer and winter. VOC concentrations often exceeded levels typically found in residential indoor air, e.g. benzene concentrations reached values of up to 149.1 µg m^− 3. Overall concentrations were 40% higher in summer, with temperatures inside the cars reaching up to 70 °C. The most frequently detected phthalates were di-n-butyl-phthalate and bis-(2-ethylhexyl) phthalate in concentrations ranging from 196 to 3656 ng m^− 3.     

Contribution of tobacco smoke to environmental benzene exposure in Germany

The concentrations of environmental tobacco smoke (ETS) constituents including benzene were measured in the living rooms of 10 nonsmoking households and 20 households with at least one smoker situated in the city and suburbs of Munich. In the city, the median benzene levels during the evening, when all household members were at home, were 8.1 and 10.4 μg/m³ in nonsmoking and smoking homes, respectively. The corresponding levels of 3.5 and 4.6 μg/m³ were considerably lower in the suburbs. Median time-integrated 1-week benzene concentrations in the city were 10.6 μg/m³ in nonsmoking homes and 13.1 μg/m³ in smoking homes. In the suburbs, the corresponding values were 3.2 and 5.6 μg/m³. While the benzene concentrations in nonsmoking homes located in the city were significantly higher (p < 0.05) than in suburban nonsmoking households, no difference was found between smoking and nonsmoking households located either in the city or in the suburbs. Individual exposures to benzene and to specific markers for tobacco smoke of all household members (82 nonsmokers and 32 smokers) were determined by questionnaire, personal monitoring, and biomonitoring. Within the city, the benzene exposure determined by personal samplers was 11.8 μg/m³ for nonsmokers living in nonsmoking homes and 13.3 μg/m³ for nonsmokers in smoking homes. The corresponding values for nonsmokers living in the suburbs were 5.9 and 6.9 μg/m³, respectively. Neither difference was statistically significant. Nonsmokers living in nonsmoking households in the city had significantly higher exposure to benzene compared to their counterparts living in the suburbs (personal samplers: 11.8 vs 5.9 μg/m³, p < 0.001; benzene in exhalate: 2.4 vs. 1.1 μg/m³, p < 0.05; trans,trans-muconic acid excretion in urine: 92 vs. 54 μg/g creatinine, p < 0.05). Nonsmokers from all households with smokers were significantly more exposed to benzene than nonsmokers living in the nonsmoking households (personal samplers: 13.2 vs. 7.0 μg/m³, p < 0.05; benzene in exhalate: 2.6 vs. 1.8 μg/m³, p < 0.01; trans,trans-muconic acid excretion in urine: 73 vs. 62 μg/g creatinine), but the contribution of ETS to the total benzene exposure was relatively low compared to that from other sources. Analysis of variance showed that at most 15% of the benzene exposure of nonsmokers living in smoking homes was attributable to ETS. For nonsmokers living in nonsmoking households benzene exposure from ETS was insignificant.     

Experimental measurements of aerosol concentrations in offices

A new automated version of the piezoelectric microbalance measures the mass concentration of airborne particles smaller than a preselected aerodynamic cutoff diameter. It is designed for near-real-time, unattended, round-the-clock measurements of nearly any aerosol environment inhabited by humans. The instrument uses an electrostatic precipitator to deposit particles with greater than 95% efficiency onto a piezoelectric quartz crystal sensor which is able to detect a deposit of 0.005 μg. The precipitator and sensor are nearly identical to those in the portable instrument reported previously. Measurements comparing within ± 15% with gravimetrically measured filter samples are documented for a wide variety of aerosols in the 50 μg/m³ to 5.5 mg/m³ range. The instrument measures particles from 10 μm down to 0.01 μm in diameter, including submicron combustion smokes and metallic fumes. The piezoelectric microbalance technique senses the mass concentration of the aerosol, rather than light scattering properties as is done by photometers and nephelometers. The piezobalance, with 1 L/min sample flow, is more sensitive than any other mass-sensing instrument, making it especially suited for low concentration indoor measurements, even below 50 μg/m³. An automatic piezobalance recently measured respirable aerosol mass concentrations in several offices. Each measurement was the average concentration during a 30-min period. The 24-h/day measurements continued for several days. Especially interesting is the diurnal pattern, both for offices with and without smokers. The effect of a single nearby smoker was clearly illustrated when the smoker was absent one day in the middle of a week. Normal daytime peak concentrations in that office reached 80–110 μg/m³ with a smoker present, but only 50–60 μg/m³ when the smoker was absent. Curious smokers who briefly stopped byt o see the instrument caused single half-hour averages to triple, to values as high as 294 μg/m³ in one office.     

Growth response of Scenedesmus to different concentrations of copper, cadmium, nickel, zinc, and lead

The fresh water alga Scenedesmus was cultured in graded concentration of Cu, Cd, Ni, Zn, and Pb to evaluate the effect of these cations on the growth response of Scenedesmus. The effective concentration of metal which depressed the Scenedesmus growth for Cu was 0.5 mg l⁻¹, for Cd 0.5 mg l⁻¹, for Ni 2 mg l⁻¹, and for Zn 2 mg l⁻¹. The alga exhibited tolerance for high Pb concentrations up to 30 mg l⁻¹. Exposure of a Scenedesmus cell to each metal revealed anatomical changes and chloroplast disruption especially at high metal concentrations.     

The influence of ventilation on indoor/outdoor air contaminants in an office building

The air quality in a newly built preschool was investigated in a longitudinal study. Typical air contaminants emanating from building materials were determined, their variation over time (0–18 months) was measured, and the influence of the ventilation system (81%–91% recirculation of return air) on contaminant concentrations was studied. Volatile organic compounds were sampled by adsorption on porous polymer, analysed by a GC/FID system, and identified by MS. A spatial build-up in concentration (ppb or μg/m³ levels) is evident for all the organic compounds, as well as for CO₂, from the outdoor air, through the ventilation system, and through the rooms to the exhaust air. The longitudinal comparison over time shows that all the organic compounds decline in concentration mainly within the first 6 months of occupancy: 1-butanol 4–14 times, toluene and pentanal + hexanal 2–4 times, while formaldehyde remained at a constant low level of 90 ppb (110 μg/m³). It is difficult to believe that the problems of poor air quality in 100 preschools in Stockholm are caused by the organic compounds alone unless interactions occur. A preschool building needs to be gassed off during the first 6 months after its construction with no recirculation of return air allowed (outdoor air rate approx 4–5 ach). During at least 1–2 additional years, it is desired that the recirculation rate of return air is restricted, perhaps to 50%.     

The effect of acidification on abiotic interactions of dissolved humic substances, iron and phosphate in epilimnetic water from the humex Lake Skjervatjern

The responses to pH of abiotic interactions between dissolved humic substances, iron and phosphate were investigated by examining redistributions of ⁵⁵FeCl₃ and ³²PO₄³⁻ added to epilimnetic lakewater from Lake Skjervatjern. The simultaneous movement of ⁵⁵Fe and ³²P to fractions of 10 000–20 000 and > 100 000 Daltons nominal molecular weight, as indicated by Sephadex gel filtration, diminished in response to decreasing pH. Variations in transformations to larger molecular size fractions with incubation time revealed by gel filtration were erratic, but indicated that transformations of added ⁵⁵Fe and ³²P are complete after circa 24 h. Movement of ³²P to particle size fractions (>0.2 μm) was not dependent on pH, whilst transformations of ⁵⁵Fe to material of particle size increased as pH was lowered. Precipitation of added ⁵⁵Fe and ³²P was minimal at all pH values tested. Responses of precipitation losses to pH were not coincident for both radionuclides.     

Present status of Rn in groundwater in Extremadura

Radon-222 was measured in groundwater sources of Extremadura (Spain), analyzing 350 samples from private and public springs, wells, and spas by liquid scintillation counting (LSC) and gamma spectrometry. The ²²²Rn activity concentrations ranged from 0.24 to 1168 Bq L⁻¹. The statistical analysis showed a log-normal distribution with a mean of (111 ± 7) Bq L⁻¹ and a median of (36 ± 3) Bq L⁻¹. A hydrogeological study revealed correlations between the activity concentration and the aquifer material's characteristics. A map of ²²²Rn in groundwater was elaborated and compared with the natural gamma radiation map for this region. About 35% of the samples showed ²²²Rn activity concentrations above the Euratom recommended limit of 100 Bq L⁻¹. Three uranium series radionuclides (²³⁸U, ²³⁴U, and ²²⁶Ra) were also assayed by alpha-particle spectrometry, estimating the annual effective dose due to the presence of these natural radionuclides in drinking water.