Daily intake of arsenic, cadmium, mercury, and lead by consumption of edible marine species

The daily intake of arsenic (As), cadmium (Cd), mercury (Hg), and lead (Pb) through the consumption of 14 edible marine species by the general population of Catalonia, Spain, was estimated. Health risks derived from this intake were also assessed. In March-April 2005, samples of sardine, tuna, anchovy, mackerel, swordfish, salmon, hake, red mullet, sole, cuttlefish, squid, clam, mussel, and shrimp were randomly acquired in six cities of Catalonia. Concentrations of As, Cd, Hg, and Pb were determined by ICP-MS. On the basis of recent fish and seafood consumption data, the daily intake of these elements was calculated for eight age/sex groups of the population. The highest As concentrations were found in red mullet, 16.6 microg/g of fresh weight, whereas clam and mussel (0.14 and 0.13 microg/g of fresh weight, respectively) were the species with the highest Cd levels. In turn, swordfish (1.93 microg/g of fresh weight) and mussel and salmon (0.15 and 0.10 microg/g of fresh weight) showed the highest concentrations of Hg and Pb, respectively. The highest metal intake through fish and seafood consumption corresponded to As (217.7 microg/day), Cd (1.34 microg/day), and Pb (2.48 microg/day) for male seniors, whereas that of Hg was observed in male adults (9.89 microg/day). The daily intake through fish and seafood consumption of these elements was compared with the provisional tolerable weekly intakes (PTWI). The intakes of As, Cd, Pb, and total Hg by the population of Catalonia were below the respective PTWI values. However, the estimated intake of methylmercury for boys, 1.96 microg/kg/week, was over the PTWI.     

Fish contamination and human exposure to mercury in Tartarugalzinho River,Amapa State,Northern Amazon,Brazil. A screening approach

This study reports for the first time, the Hg concentrations in the fish fauna of the Tartarugalzinho river basin - an important gold mining region in Amapa State, Northern Amazon - and evaluates human exposure to Hg due to fish consumption in the area. We analyzed 16 fish species (carnivorous and omnivorous) common in the aquatic environment of the Tartarugalzinho area and which are mostly consumed by the local population. Mercury concentrations in fish ranged from 35 µg.kg-1 to 1,225 µg.kg-1. Among the analyzed fish, 8 species (50%) presented Hg concentrations higher than 500 µg.kg-1, the U.S. Food and Drug Administration (FDA) Action Level for concentration of Hg in fish. No statistical difference was observed between Hg mean concentrations in carnivorous and omnivorous fish. Within a given species, Hg concentrations were positively correlated with fish size or weight. The Hg concentration ratio between fish and water showed values higher than 50,000. Human exposure was estimated through the daily Hg intake obtained through interviews with the local population on the amount and species of fish consumed and the Hg concentration in the fish. The estimated average daily intake was 114 µg.day-1. This amount is approximately one-half of the WHO recommended provisional tolerable Hg weekly intake. At screening level, it assumes that there is a level of exposure (e.g, USEPA's RfD = Reference of Dose) below which it is unlikely for even sensitive populations to experience adverse health effects. The estimated exposure level for adult humans (1.6 µg.kg-1.day-1) was nearly 5 times greater than Hg RfD (0.3 µg.kg-1.day-1). The results suggest a widespread Hg contamination in the local fish fauna. Due to high fish Hg concentrations and high fish intake by local population, environmental exposure to Hg is also high, presenting a health risk to population.     

Perchlorate Distribution, Excretion, and Depuration in Prairie Voles and Deer Mice

A study on perchlorate distribution was conducted in male adult prairie voles (Microtus ochrogaster). Excretion via urine was the major pathway for perchlorate fate in the body, with the highest concentrations of perchlorate detected in urine after exposure to perchlorate through drinking water [250 μg/ml Mg(ClO₄)₂], and an average of 34% and 88% of perchlorate intake recovered in urine in the 4- and 8-h exposure groups, respectively. Perchlorate mass in kidney, thyroid, blood, and urine were related to perchlorate intake (254.5–2687.7 μg). Perchlorate excretion and depuration patterns via urine were tested further using male adult deer mice (Peromyscus maniculatus). Animals were exposed to perchlorate through dosed drinking water (0, 17, 165, and 1600 ng/ml). Perchlorate concentrations in urine showed a significant difference among the three dosed groups during a 28-day exposure period. However, no difference was found in urine among the three dosages in terms of mass percentage of perchlorate intake from water at each sampling time over the 28-day exposure period. Both concentrations of perchlorate and mass percentage in urine reached a steady state after 1 day in all treatments. On average 46%, 46%, and 61% of perchlorate intake from water was recovered in urine over the exposure period in high, medium, and low dose groups, respectively. Including perchlorate consumption from rodent chow (1.44 ng/g), less than 46% of perchlorate intake was recovered in urine in the high and medium dose groups, and <61% in the low dose group. Three parameter first-order decay models fit the depuration curve very well, with r?>?0.99 in both the low and high dose groups; half-lives of perchlorate in deer mice were estimated as 9.12 and 7.25 h in the low and high dose groups, respectively. Endogenous generation of perchlorate and/or some degree of retention or metabolism of perchlorate may occur in deer mice, based in part on the uncompleted mass balance in the excretion and depuration experiments. The data reported herein should provide additional insight for perchlorate fate determination in animals and humans and valuable information for perchlorate risk assessment in the environment, especially wildlife.     

Mercury in Biota and Surficial Sediments from Coatzacoalcos Estuary, Gulf of Mexico: Distribution and Seasonal Variation

Variation of mercury (Hg) in sediments and biota from Coatzacoalcos estuary during the dry, rainy and windy seasons was estimated. In sediments, Hg concentrations ranged from 0.07 μg g^?1 in site 13 (Ixhuatepec) located upstream, to 1.06 μg g^?1 in site 3 (Coatzacoalcos river), located in the industrialized area. Highest enrichment factor (EF) and index of geoaccumulation (I _geo) in surficial sediments were 53 and 5.1 respectively. From EF and I _geo, it is considered that Coatzacoalcos estuary is from moderately contaminated to contaminated. In most fish species from Coatzacoalcos estuary, the sequence of Hg concentration was liver>muscle>gills. Average Hg concentrations in soft tissue of bivalves ranged from 0.09 μg g^?1 in Corbicula fluminea to 0.18 μg g^?1 in Polymesoda caroliniana. Biota-sediment accumulation factor (BSAF) ranged from 0.9 in P. caroliniana during the rainy season (site 4) to 3.8 in P. caroliniana from the same site during the windy season.     

Mercury exposure in humans through food consumption from the Everglades of Florida

In March 1989, The Florida Department of Health and Rehabilitative Services (HRS) issued a Health Advisory recommending the limited consumption of several fish species caught from the Everglades region of South Florida due to elevated methylmercury (MeHg) levels (average 2–3 ppm in fish meat). There were no reports of clinical MeHg poisoning in humans in Florida, although deaths of Florida panthers were attributed to mercury (Hg). poisoning. This study evaluated the extent of MeHg exposure in persons eating contaminated fish in the Everglades region. Populations at risk were identified including sport fishermen, Everglades Residents and subsistence fishermen. Over 1700 individuals were approached; those who had eaten fish or wildlife from the contaminated areas at least once/month for the prior three months were asked to participate. Three hundred and fifty (350) participants completed a brief questionnaire and provided a hair sample for Hg analysis. In 119 (36%) of individuals with levels above the limits of detection, the mean total Hg in hair was 3.62±3.0μg/g [± standard deviation] with a range of 1.28 – 15.57. The most at risk populations identified with respect to Hg levels were Blacks and men. Although the majority of the participants had fished in the Everglades for many years (>15 years), they reported relatively low intake of fish and had low hair Hg levels compared with similar populations in prior studies of other populations at risk. Although 71% of participants knew of the State Health Advisories concerning ingestion of Hg contaminated fish from the Everglades, this did not change their consumption habits. In addition, Blacks, individuals of lower income and of lower education levels were less likely to know about the Health Advisories. Given recent studies of neurologic effects from relatively low in utero MeHg exposure, the continuation of the Mercury Health Advisories and wildlife monitoring in the Everglades are warranted, especially for women of childbearing age and children. However, public education must be targeted for the populations at risk identified in this study in order to reach these populations more effectively.     

Mass balance and systemic uptake of mercury released from dental amalgam fillings

The release of mercury (Hg) from dental amalgam fillings has been verified by several authors. In this study, the emission rate of Hg°-vapor from the oral cavity (O-Hg) and the urinary Hg-excretion rate (U-Hg) have been studied with 34 healthy individuals. In ten cases, the urinary excretions of silver (U-Ag) and the fecal excretions of Hg and Ag (F-Hg, F-Ag) were also monitored. All variables, except U-Ag, were significantly related to the load of amalgam. According to this study, an individual with a moderate load of amalgam, i.e. 30 restored surfaces, is predicted to exhibit the following emission rates: O-Hg=22, U-Hg=3, F-Hg=60 and F-Ag=27 μg/d (d=24 hours), consistent with a gross mass balance for Hg of approximately 60 μg/d. The corresponding systemic uptake of Hg was estimated to 12 μg/d based on external data relating air Hg°-exposures to urinary Hg-excretions. The worst case individual showed a gross mass balance of 200 μg Hg/d connected to a systemic uptake of 70 μg Hg/d. These values were compared to the average intake of total-Hg by a Swedish diet (2 μg/d) and to the WHO's tolerable value for intake of total-Hg by food (45 μg/d). Upscaled to the entire Swedish population (8 mill.), the data suggests a fecal/urinary emission to the environment of 100 kg Hg yearly originating from a population load of amalgam fillings containing 90,000 kg of Hg.     

Mercury Methylation Capacity and Removal of Hg Species from Aqueous Medium by Cyanobacteria

Most technologies used for decontamination presents good results for high concentrations, but limitations for lower ones. The desirable Hg concentration in the water is extremely low because of its toxicity. The aims of this study were to evaluate inorganic mercury (Hg²⁺) and methylmercury (CH₃Hg⁺) toxicity in Nostoc paludosum, to assess the potential of this cyanobacteria strain to remove these Hg species from aqueous medium and also to investigate Hg methylation by the cyanobacteria. CH₃Hg⁺ determination was performed by gas chromatography-pyrolysis-atomic fluorescence spectrometry in cultures exposed to a concentration of 20 μg L^?1 for 30 days. Both Hg species were removed from the supernatant, ranging from 73 to 96% of Hg²⁺ and from 73 to 95% of CH₃Hg⁺. Ultrastructural Hg²⁺ effects in the cyanobacteria cells investigated by transmission electron microscopy revealed higher production of glycogen, cyanophycin, and intrathylacoidal spaces than the control group. When Hg was added to the culture in the form of CH₃Hg⁺, a decrease corresponding to approximately 60% of the initial concentration due to Hg volatilization was observed. The production of CH₃Hg⁺ by the cyanobacteria was detected in concentrations near the limit of detection (0.0025%) of the bioaccumulated THg. This is an advantage for biotechnological decontamination applications, as CH₃Hg⁺ is a very toxic specie and can be bioaccumulated and biomagnified. The results demonstrated that cyanobacteria cells are an efficient alternative to retain and/or remove Hg at low concentrations and they constitute a potential tool for a “final cleaning” of contaminated waste water.     

Risk Assessment of Mercury in Alta Floresta. Amazon Basin - Brazil

In the last 15 years gold mining activity has been the main source of the mercury (Hg) emissions into the atmosphere in the Amazon Basin. The first phase of gold production takes place in remote areas. In general the second one happens in the local urban area, where the gold is commercialized and sent to the great economic centers. In the last 3 years, this activity started to decline as a consequence of the high cost of the gold production but in the Municipality of Alta Floresta, the gold trade still plays an important role in the local economy. This paper addresses the assessment of the Hg exposure scenarios and their quantitative risk for inhalation of metallic Hg vapor and for ingestion of total Hg, using indirect exposure measurements, for different age groups of the urban area of Alta Floresta. This work took into account the field study which provided background information, such as characteristics of local and regional environment, Hg concentrations in different environmental media, and the character of the local urban population. The mean levels of Hg in the atmosphere of the urban area ranged from 210 ng/m³ to 880 ng/m³. Alta Floresta has no riverside population and there is a low fish consumption rate of 8 g/d among the general population. However, mercury levels in locally consumed carnivorous fish, ranged from 0.3 to 3.6 mg/kg, depending on the species and on the period of the year. The levels of mercury in soil surrounding the residential areas near the Hg emissions sources, ranged from 0.05 to 4.10 mg/kg. Hg in soil may represent an important source of mercury ingestion for local children up to 4 years of age. The mean Hazard Index estimated for the general adult population was 1.4. For the general population, regarding the number of persons exposed in the urban area, inhalation of metallic Hg vapor is the main route of exposure. The results for water ingestion for all groups are negligible. For families of fishermen the Hazard Index was estimated to be 9.3, with a contribution of 92% from fish ingestion.     

Perfluorinated compounds in human blood, water, edible freshwater fish, and seafood in China: daily intake and regional differences in human exposures

Despite the growing public interest in perfluorinated compounds (PFCs), very few studies have reported the sources and pathways of human exposure to these compounds in China. In this study, concentrations of 10 PFCs were measured in human blood, water (tap water and surface water), freshwater fish, and seafood samples collected from China. On the basis of the data, we calculated daily intakes of PFCs, regional differences in human exposures, and potential risks associated with ingestion of PFCs from diet, drinking water, and indoor dust for the Chinese population. Perfluorooctane sulfonate (PFOS) was the most predominant PFC found with a mean concentration of 12.5 ng/mL in human blood from Tianjin and 0.92 ng/g wet wt in freshwater fish and seafood; perfluorooctanoic acid (PFOA) was the major PFC found in drinking water at a concentration range of 0.10 to 0.92 ng/L. The estimated daily intake of PFOS and PFOA via fish and seafood consumption (EDI(fish&seafood)) ranged from 0.10 to 2.51 and 0.13 to 0.38 ng/kg bw/day, respectively, for different age groups (i.e., toddlers, adolescents and children, and adults) from selected locations (i.e., Tianjin, Nanchang, Wuhan, and Shenyang). The EDI(fish&seafood) of PFCs decreased (p < 0.05) with age. The estimated daily intake of PFOS and PFOA via drinking water consumption (EDI(drinking water)) ranged from 0.006 to 0.014 and 0.010 to 0.159 ng/kg bw/day, respectively. Comparison of EDI(fish&seafood) and EDI(drinking water) values with those of the modeled total dietary intake (TDI) of PFCs by adults from Tianjin, Nanchang, Wuhan, and Shenyang showed that contributions of fish and seafood to TDI of PFOS varied depending on the location. Fish and seafood accounted for 7%, 24%, 80%, and 84% of PFOS intake in Nanchang, Shenyang, Wuhan, and Tianjin, respectively, suggesting regional differences in human exposure to PFOS. Drinking water was a minor source of PFOS (<1%) exposure in adults from all the study locations.     

Impact of the state-of-the-art of flue gas cleaning on mercury species emissions from coal-fired steam generators

When balancing the element mercury (Hg) two coal-fired power plant units — one with slag tap boilers (ST, 2 × 220 MW) and one with a dry bottom boiler (DB, 475 MW) were compared. Both systems are provided with electrostatic precipitators (ESP), nitrogen oxides removal (DeNO_x) and flue gas desulfurization (FGD) systems. The Hg in the flue gas is predominantly in gas phase. Only 15 % of the Hg introduced by the coal leaves the unit with the bottom or fly ash. Depending on the operating mode, 30 to 40 % of the Hg is separated in the FGD systems. The overall separation rate for the total system ranges between 45 to 55 %, the residue is emitted in the form of gaseous Hg species. At full load, the Hg concentration in the cleaned gas is less than 6 μg/m³. In the flue gas path of another dry bottom boiler (DB1, 480 MW) the concentrations of the gaseous species of bivalent mercury (Hg²⁺), elemental mercury (Hg⁰), and total mercury content (Σ Hg) were determined. The sum of the concentrations of Hg²⁺ and Hg⁰ is in agreement with the measurement of Σ Hg. Directly downstream of the boiler Hg²⁺ dominates with 77 %, while Hg⁰ amounts to 23 %. In the high-dust DeNO_x system Hg⁰ is oxidized almost completely to Hg²⁺ (96 %). Air heater and electrostatic precipitator do not influence the Hg species concentrations. The FGD system eliminates approximately 80 % of the Hg²⁺. At the same time the quantity of Hg⁰ increases by the factor 10. In the cleaned gas Hg⁰ dominates with 76 % as compared to Hg²⁺ with 24 %. At full load the concentration of Σ Hg in the cleaned gas is also below 6 μg/m³.     

Mercury Accumulation in Foliage over Time in Two Northern Mixed-Hardwood Forests

Concentrations of mercury (Hg) in live foliage increased ten-fold from spring bud break (mean ± std. dev. from bothsites: 3.5±1.3 ng g^-1) to autumn litterfall(36±8 ng g^-1). Mercury in foliage did not behavesimilarly to eight other elements with known soil or aerosolsources (Aluminum (Al), Vanadium (V), Strontium (Sr), Rubidium(Rb), Copper (Cu), Zinc (Zn), Barium (Ba), and lead (Pb)),suggesting that Hg originated from a distinct pathway. Based onmeasured and modeled data, uptake of only 25% of the availableambient dry deposited Hg⁰ could explain all of the Hgmeasured in foliage throughout the growing season. Estimates ofgaseous elemental Hg (Hg⁰) uptake from soil water accountedfor 3–14%% of the Hg in litterfall. Mercury deposition toforested sites in the Lake Champlain and Lake Huron basins washighest in litterfall (40%), followed by total throughfall(33%), and precipitation (27%). The Hg flux in litterfall was15.8±1.9~μg m^-2 yr^-1 to the Lake ChamplainWatershed in 1995 and was 11.4±2.8~μg m^-2 yr^-1 to the Lake Huron Watershed in 1996. In comparison, the Hg fluxes in precipitation and total throughfall were 9.0±0.6 and 11.6±0.7~μg m^-2 yr^-1in the Lake Champlain Watershed (1995), and 8.7±0.5 and 10.5±1.0~μg m^-2 yr^-1 in the Lake Huron Watershed (1996).     

Determination of Mercury Content in a Shallow Firn Core from Greenland by Isotope Dilution Inductively Coupled Plasma Mass Spectrometry

The total mercury content was determined in 6 cm sections of a shallow 7 m firn core and in surrounding surface snow from Summit, Greenland (elevation: 3238 m, 72.58^°N, 38.53^°W) collected in May 2001 by isotope dilution cold-vapor inductively coupled plasma mass spectrometry (ID-CV-ICP-MS). The focus of this research was to evaluate the capability of the ID-CV-ICP-MS technique for measuring trace levels of Hg typical of polar snow and firn. Highly enriched ²⁰¹Hg isotopic spike is added to approximately 10 mL melted core and thoroughly mixed. The Hg²⁺ in the sample is reduced on line with tin(II) chloride (SnCl₂) and the elemental Hg (Hg^°) vapor pre-concentrated onto gold gauze using a commercial amalgam system. The Hg is then thermally desorbed and introduced into a quadrupole ICP-MS. The blank-corrected Hg concentrations determined for all samples ranged from 0.25 to 1.74 ng/L (ppt) (average 0.59 ± 0.28 ng/L (1σ)) and fall within the range of those previously determined by Boutron et al. [Geophys. Res. Lett. 25, 1998, 3315–3318] (≤ 0.05–2.0 ng/L) for the Summit site. The average blank value was 0.19 ± 0.045 ng/L (n = 6, 1σ) and the method detection limit was 0.14 ng/L. The Hg values specifically for the firn core range from 0.25 to 0.87 ng/L (average 0.51 ± 0.13 ng/L (1σ)) and show both values declining with time and larger variability in concentration in the top 1.8 m.     

Total mercury and methylmercury mass balance in an alkaline,hypereutrophic urban lake (Onondaga Lake,NY)

A total mercury (total Hg) and methylmercury (CH₃Hg) mass balance was developed for Onondaga Lake, NY, based on sampling of tributaries, sediments, water column, and biota in 1992. Thein situ flux of total Hg and CH₃Hg from sediments to the overlying water and the rate of net CH₃Hg production in the water column were determined experimentally. Fluxes from atmospheric deposition, groundwater, and volatilization were estimated from limited field data and the literature. Ultraclean sampling and analytical techniques developed specifically for Hg were used. Results indicate that tributaries contribute the majority of total Hg entering the lake (13.6 kg in 1992). Other sources of total Hg included groundwater flux (0.02 kg), atmospheric deposition (0.44 kg), and flux from sediments (0.056 kg). Net sedimentation (11.1 kg), outflow (2.8 kg), and volatilization (0.016 kg) were sinks for total Hg. The two major sources of CH3_Hg were tributaries (0.26 kg) and net CH₃Hg production in the water column (0.60 kg). Flux from sediments accounted for only 0.017 kg CH₃Hg. Net sedimentation (0.47 kg), outflow (0.24 kg), and net uptake, by fish (0.20 kg) were sinks for CH₃Hg. Gross sedimentation of CH₃Hg exceeded net sedimentation by 90%, suggesting that release of CH₃Hg from settling particles is a significant process.     

Mercury reactions in the human mouth with dental amalgams

This is a preliminary study of the reactions of mercury (Hg) in the human mouth with dental amalgams. It was conducted by analysing saliva samples from subjects with amalgam fillings and control subjects with no amalgams. Samples were collected both prior to and after cleaning the mouth. These samples were analyzed for elemental mercury (Hg⁰), inorganic mercury (Hg²⁺) and methylmercury (MeHg). We concluded that the concentrations after cleaning represented the systemic concentrations. Hg²⁺ and MeHg were found in all systemic samples from both subjects and controls, while Hg⁰ was found only in the samples from subjects with amalgams. In the control group, the concentrations found before and after cleaning the mouth were equivalent. In the amalgam group, concentrations of Hg²⁺ found before cleaning the mouth were 10 to 40 times higher than those found after cleaning, suggesting that the oxidation reaction of Hg° into Hg²⁺ takes place. For MeHg, a similar but less pronounced pattern as Hg²⁺ was found, supporting methylation in the mouth.     

Mercury speciation adsorption (MESA) method for combustion flue gas: Methodology,artifacts, intercomparison,and atmospheric implications

Chemical speciation of mercury (Hg) in a wide variety of combustion flue gas matrices has been determined using the mercury speciation adsorption (MESA) method. The MESA sampling system for gas phase Hg species employs a series of heated, solid phase adsorbent traps. Flue gas oxidized Hg species (Hg(II) and MMHg) are adsorbed by a potassium chloride (KCl) impregnated soda lime sorbent. Elemental Hg (Hg⁰) is collected by an iodated carbon sorbent after passing through the KCl/soda lime sorbent. Total Hg (Hg_t) is determined by summation of species. In the laboratory, cold vapor atomic fluorescence spectroscopy (CVAFS) is used for detection of Hg collected on the solid sorbents, after appropriate sample digestion and preparation. The MESA method has been evaluated for species stability, matrix effects, breakthrough, artifacts and precision. Based on eight duplicate samples a mean precision of 6.8% 11% and 4.5% (relative percent difference) has been calculated for Hg⁰, Hg(II) and Hgt respectively. Intercomparison of the MESA method with other methods shows very good agreement for Hgt. Mass balance calculations at 5 sites range from 75 to 140%, with a mean of 97±25%. Overall mean speciation results from 19 separate determinations suggest that Hg(II) has a 1 sigma range of 40 to 94% in coal combustion flue gas at, the inlet to pollution control devices.     

Human exposure to mercury may decrease as acidic deposition increases

It has been hypothesized that human mercury (Hg) exposure via fish consumption will increase with increasing acidic deposition. Specifically, acidic deposition leads to reduced lake pH and alkalinity, and increased sulphate ion concentration ([SO₄ ^2?]), which in turn should cause increased Hg levels in fish, ultimately resulting in increased human Hg exposure via fish consumption. Our empirical test of this hypothesis found it to be false. We specifically examined Hg levels in the hair of Ontario Amerindians, who are known consumers of fish from lakes across the province, and observed a weak negative association with increasing sulphate deposition. An examination of Hg levels in lake trout, northern pike and walleye, three freshwater fish species commonly consumed by Ontario Amerindians, found a similar weak negative association with increasing sulphate deposition. Further analysis of these fish data found that fish [Hg] was most significantly (positively) associated with lake water concentrations of dissolved organic carbon (DOC), not pH, alkalinity or [SO₄ ^2?]. Lake DOC levels are lower in regions of greater acidic deposition. We propose an alternate hypothesis whereby human Hg exposure declines with increasing acidic deposition. In particular, we propose that increasing sulphate deposition leads to reduced lake DOC levels, which in turn leads to lower Hg in fish, ultimately reducing human Hg exposure via fish consumption.     

Uptake of Uranium by Lettuce (Lactuca sativa L.) in Natural Uranium Contaminated Soils in Order to Assess Chemical Risk for Consumers

Uranium mining activity in Cunha Baixa (Portugal) village has left a legacy of polluted soils and irrigation water. A controlled field experiment was conducted with lettuce (Lactuca sativa L.) in an agricultural area nearby the abandoned mine in order to evaluate uranium uptake and distribution in roots and leaves as well as ascertain levels of uranium intake by the local inhabitants from plant consuming. Two soils with different average uranium content (38 and 106 mg/kg) were irrigated with non-contaminated and uranium contaminated water (<20 and >100 μg/l). A non-contaminated soil irrigated with local tap water (<1 μg/l uranium) was also used as a control. Uranium in lettuce tissues was positively correlated with soil uranium content, but non-significant differences were obtained from contaminated soils irrigated with different water quality. Uranium in plants (dry weight) growing in contaminated soils ranged from 0.95 to 6 mg/kg in roots and 0.32 to 2.6 mg/kg in leaves. Lettuce bioconcentration is more related to available uranium species in water than to its uranium concentration. Translocated uranium to lettuce leaves corresponds to 30% of the uranium uptake whatever the soil or irrigation water quality. A maximum uranium daily intake of 0.06 to 0.12 μg/kg bodyweight day was estimated for an adult assuming 30 to 60 g/day of lettuce is consumed. Although this value accounts for only 10% to 20% of the recommended Tolerable Daily Intake for ingested uranium, it still provides an additional source of the element in the local inhabitants’ diet.     

Mercury and polychlorinated biphenyls in striped bass (Morons saxatilis) from two nova Scotia Rivers

Striped bass (Morone saxatilis) collected from the Annapolis and Shubenacadie Rivers in Nova Scotia, Canada, were analyzed for Hg in four tissues and for PCB's in two tissues. Average Hg concentrations in the muscle, liver, kidney, and gonad of 3.9 kg fish from Annapolis River were 0.77, 0.79, 0.26, and 0.07 μg g^?1, respectively, and the corresponding values for the much smaller, 1.5 kg, fish from the Shubenacadie River were 0.51, 0.27, 0.24, and 0.06 μg g^?1. The PCB concentrations in the muscle tissues of fish from Annapolis and Shubenacadie Rivers are 0.02 and 0.01 μg g^?1, respectively, while the concentrations in gonads are 1.4 and 0.04 μg g^?1 The observed lack of recruitment of striped bass in the Annapolis River may be related to high PCB concentrations in the gonad tissue.     

Food consumption patterns in an adult urban population in Beirut, Lebanon

OBJECTIVES: To investigate, measure and assess the food consumption pattern of the adult population living in Beirut, Lebanon, and to identify inadequate or excessive intake of food groups particularly linked to non-communicable diseases. DESIGN: A cross-sectional food consumption survey was conducted in 2001. Dietary habits were assessed by means of a quantitative food-frequency questionnaire. SETTING: Dietary survey of the urban population (Beirut). SUBJECTS: Random sample of 444 adult subjects (aged 25-54 years) in Beirut. RESULTS: The mean consumption of food by the study population was estimated to be 3,030 g day(-1), providing an energy intake of 2,523.57 kcal day(-1). Fat contributed 38.9% to the average daily energy intake, protein 13.4% and carbohydrates 47.2%. Mean consumption of fruits and vegetables was approximately 367 g day(-1) and 45.3% of subjects consumed less than the recommended 400 g daily. Cereals contributed 324.5 g day(-1), providing 35.0% of daily energy intake, with bread being the most highly consumed (146.2 g day(-1)) in this food group. The mean intake of meat and poultry products was 91.7 g day(-1) and provided 8.8% of daily energy intake, with consumption of butchery products especially beef being the highest (47.6 g day(-1)) followed by poultry (36.1 g day(-1)). A low consumption of fish was noted (19.7 g day(-1)), with 73.6% of subjects consuming less than the recommended 2 servings of fish per week. Dairy products contributed 243.1 g day(-1) or 10.9% of daily energy intake, and milk was the least consumed dairy product (56.8% of consumers). The intake of added fats and oils, excluding those in cooked recipes, was 20.4 g day(-1); olive oil was not used in cooking but was added solely at the table and its mean intake was 5 g day(-1). The consumption of butter was low (0.86 g day(-1)) and vegetable oil was the type of fat mostly used in cooking. The average intake of alcoholic beverages was low (33.6 g day(-1)), accounting for 0.7% of total energy intake. Women had significantly higher intakes of milk, dairy products, vegetables and coffee than men (P < 0.05). The percentage of women who reported the use of low-fat items was significantly higher than that of men. Younger people (25-34 years) ate significantly more meat, sugar, alcoholic beverages and soft drinks, and consumed significantly less cooked vegetables and legumes, than older ones (P < 0.05). CONCLUSIONS: The rather high contribution of fat to daily energy intake, the low intake of fish and the relatively high percentage of people consuming less than the recommended amount of fruits and vegetables observed in this study suggest that the adult Lebanese population is at increased risk of cardiovascular diseases, obesity and other non-communicable diseases, which provides the basis for recommending increased intakes of fish, particularly fatty fish, and fruits and vegetables.