Flux of heavy metal accumulation in various organs of the intertidal marine blue crab, Portunus pelagicus (L.) from the Kuwait coast after the Gulf War.

The metal levels of arsenic, chromium, copper, lead, magnesium, manganese, selenium, vanadium, and zinc concentrations were determined in various body organs, viz., hepatopancreas, gills, gonad, gastric stomach, and muscle of the blue crab, Portunus pelagicus (Crustacea: Decapoda) to assess the bioaccumulation of metals associated with petroleum input a decade after the 1991 Gulf War oil spillage. Sample solutions prepared were analyzed using an atomic absorption spectrophotometry. High concentrations of Zn and Cu in the muscle and hepatopancreas tissues were a strong indicative of high exposure of P. pelagicus to these metals. However, muscle tissue had been found to accumulate the highest values for all metal speciations analyzed. Copper, zinc, and chromium in samples collected from Station II covering the Kuwait City area were often in excess of those present in Station I and III. Arsenic, lead, magnesium, manganese, selenium, and vanadium were greater in individuals obtained from Station I. A significant correlation was found to exist between Se and V in crab muscle with a surge in Se metal concentration, which was found to be inversely proportional to that of V metal concentration irrespective of the sex of the crab. The difference in patterns of metal occurrence and the significant increase in the Cu and Zn concentrations in various organs of the crab were largely associated with the 1991 Gulf War oil spill. Such results could be used as a baseline for the monitoring of the level of metals in marine organisms of future studies.     

Aeolian contributions of trace metals to marine sediments of Kuwait

Concentrations of silver, cadmium, chromium, iron, manganese, nickel, lead, vanadium, and zinc were determined in dust fallout samples from eight inland locations in Kuwait. Results were used to calculate enrichment factors for metals relative to their abundance in the continental crust using Fe as the conservative element. Five metals (Cu, Cr, Mn, Ni, and V) showed enrichment factors that were approximately unity (1.3–4.7). Higher enrichment factors for the rest (24–421) suggested an anthropogenic contribution for Ag, Cd, Pb, and Zn. However, all metals in dust fallout (except Pb and Zn) showed a degree of enrichment relative to unpolluted marine sediments that was approximately unity, suggesting a substantial aeolian contribution to trace metals in marine surface sediments. Higher enrichments for Pb and Zn probably reflect a larger input from local pollution sources. This is particularly true for lead, the enrichment of which showed a stronger association with the distribution of urban population. Probable contributions of aeolian transport to a band of elevated lead concentrations in marine surface sediments are discussed.     

Lead content in roadside vegetation as indicators of atmospheric pollution

Leaves of six plant species from 31 different locations in Ibadan, Nigeria, were analysed for their lead content. The lead concentrations found ranged between 12 and 32 μg/g, 50 m or more away from the roadside, between 47 and 115 μg/g in the residential low traffic density areas, 5 m from the roadside, and between 165 and 312 μg/g in the commercial high traffic density roadsides, 5 m away from the roadside.     

Pollution profile of damodar river sediment in Raniganj-Durgapur industrial belt,West Bengal,India

This paper reports on the pollution profile of Damodar river sediment as obtained from analysis of the river sediment at suitable selected sites in the Raniganj-Durgapur industrial belt, West Bengal, India. The parameters measured include (a) silica, mixed oxide, calcium, magnesium, total water-soluble exchangeable cation and anion, chemical oxygen demand, and (b) some toxic and other elements, such as sodium, potassium, arsenic, cadmium, chromium, mercury, manganese, lead, zinc, cobalt, copper, iron nickel, phosphorus, sulphur, and vanadium. The parameters listed under (a) led to the characterization of the sediment, and those under (b) gave an index of metal pollution of the sediment. The elements were estimated by inductively coupled plasma emission spectrometry.     

Anomalous behavior of trace element magnesium in fish tissues

Six fish species were collected: summer trout (Salmo alar), rock fish (Roccus lineatus), pink snapper (Lutianus ava), croaker (Stellifer lancelatus), sheepshead (Diplodus holbrooki) and spanish mackeral (Scomberomorus maculatus). Seven trace elements were determined by flame atomic absorption spectrophotometry. The results indicate that the trace elements iron, copper, zinc, mercury, chromium, and nickel show higher levels in the livers than in the flesh of all the six fish species. Surprisingly, magnesium concentration levels were consistently higher in flesh than in the livers of all six fish species.     

Levels of metals in soils of Alcalá de Henares,Spain: human health risks

The concentrations of aluminium (Al), arsenic (As), beryllium (Be), cadmium (Cd), chromium (Cr), mercury (Hg), manganese (Mn), nickel (Ni), lead (Pb), tin (Sn), thallium (Tl), vanadium (V), and zinc (Zn) were determined in soil samples collected in Alcalá de Henares (Madrid, Spain). Human health risks derived from metal inhalation and ingestion of soils were also assessed. For noncarcinogenic risks, the current levels of metals were usually lower than those considered as safe for the general population. With respect to the potentially carcinogenic elements As, Be, Cd, and Cr, the concentrations of Be, Cd, and Cr were lower than the reference values, while the average As concentration (3.4 microg/g) was higher than the safety limit for risk cancer. In general terms, the potential human health impact of ingestion/inhalation through soils of the analyzed elements seems to be rather small.     

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.     

Comparative analysis of inorganic elements in the muscle and liver of some fish species

Four fish species were collected: brown trout, grouper, spotted tail bass, and black crappie. Fish samples were thawed and dissected. The pieces of edible muscle and liver tissues were digested in a reagent-grade nitric acid, in a constant temperature shaking-water bath at 58°C. Thirteen inorganic elements were determined by flame atomic absorption.The significant findings of this report are that inorganic elements, mercury, iron, copper, zinc, chromium, and nickel with the exception of magnesium show elevated levels in the livers than in the muscles of all the four fish species. It seems magnesium concentration levels were consistantly higher in the muscles than in the livers of all four fish species. It is found that calculations of muscle-liver ratios indicate that ratios in the range of 0.5 are preliminary indicative of environmental static conditions, whereas ratios in the range of more than one are indicative of environmental improvement.     

Trends in the dissolution of metals from sediments collected during the Umitaka-Maru cruises using the microwave-acid digestion technique

Sediment samples were collected during the research vessel Umitaka-Maru cruises in the Gulf region from 15–16 December 1993 and 15–27 December 1994, from 19 and 24 locations, respectively. These samples were subjected to trace metal analysis to determine the 1991 Gulf War oil spill environmental impact in the area. The samples investigated are texturally classified into two main sediment classes: sand and mud. The total concentrations of lead, nickel, and vanadium found in the sediments from individual stations were investigated. The differences in trace metal concentrations reflect the variation in the overall composition of their host sediments. To better appraise the trace element composition of their host sediments and to determine the factors governing the trace metal distribution, the data were sub-divided into five groups among 1993 collections and seven groups during 1994. The concentration ranges of all three metals, lead (0.2–4.85), nickel (4.90–86.00), and vanadium (2.00–38.00) varied in different stations among the groups. The partitioning of trace elements between the detrial and non-detrital fractions of the sediments shows that: 1) The high concentrations of elements in mud is coupled with the increase in the detrital fraction; 2) In muddy sand sediments, nickel is bonded to the structural lattice of detrital minerals, whereas vanadium and lead held in the environmentally mobile fraction; and, 3) In sandy mud sediments, Ni is found in the detrital fraction, whereas V to slightly less extent and Pb show their non-detrital nature. The data were compared with unpolluted sediments throughout the ROPME Sea and worldwide, so the effect of anthropogenic enrichment upon the absolute concentration of the elements is minimal.     

Variations in bottom sediment nutrient and metal concentrations in the Genesee River watershed,New York

Variations in nutrient and metal concentrations of fluvial sediment may be due to varying combinations of natural and man-made factors: basin geology, surface erosion, riverbank erosion, industrial or other cultural contamination, the presence of minerals rich in trace elements (e.g. chromite), sediment ion-exchange capacity, sediment organic content, and the presence of metallic oxides. The data reported here were obtained in a study in New York State of sediment transport from the Genesee River watershed to Lake Ontario (6,500 km²; 2,400 sq.mi.). One hundred bottom sediment samples collected over a period of a year were chemically analyzed for aluminium, chromium, copper, iron, manganese, nickel, lead, zinc, total carbon, total organic carbon, total nitrogen, and phosphorus. The metal concentrations (arithmetic means ±S.D., in μg/g) were: Al, 6,660±2,620; Cr, 14±9; Cu, 18±7; Fe, 15,060±7,312; Mn, 424±212; Ni, 23±13; Pb, 40±67; and Zn, 69±37. For the major nutrients the results (mean ±1 S.D. in %) were: total carbon, 2.06 ± 1.68; total organic carbon, 1.37 ± 1.28; total nitrogen, 0.105 ± 0.098; and phosphorus, 0.0560 ± 0.014.     

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.     

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.     

Diesel soot: Mutation measurements in bacterial and human cells

Both hot pipe and dilution chamber samples of the exhaust from a diesel (Oldsmobile 350) engine have been collected, extracted with methylene chloride and those extracts have been tested for mutagenicity in forward mutation assays in human lymphoblasts and S. typhimurium. In the absence of a metabolic activation system, the extract was significantly mutagenic to the bacteria in the range of 0 to 30 μg/ml, but introduced no mutations in human cells at concentrations up to 200 μg/ml under the same conditions of assay medium. However, when assayed in the presence of a postmitochondrial supernatant derived from rat liver, the the soot extracts were significantly mutagenic to both bacteria and human cells in the range of 50–100 μg/ml. Fractionation of the soot extract on the basis of polarity by sequential elution from a silicic acid column permitted concentration of the mutagenic activity in the alkane/toluene eluate, as determined by bacterial assays. Preliminary characterization of this fraction and preliminary studies of pure compounds leads us to suspect the alkyl substituted phenanthrenes as representing at least a significant fraction of the mutagenic activity of this alkane/toluene eluate.     

Effect of cigarette smoking on residential NO2 levels

Two studies evaluating the levels and sources of nitrogen dioxide in approximately 90 employee homes in the Richmond area with continuous sampling during the weeks of August 5, 1980, and February 9, 1981, were performed using samplers in the living room, bedroom, kitchen, and outdoors. Additional data were collected concerning appliance usage, heating/cooling plant, ventilation and cigarette smoking. Results were analyzed using BMDP routines. The largest contributor to NO₂ concentration was found to be gas-fired kitchen appliances. The mean kitchen level for homes with gas appliances during the winter study was 188 μg/m³. Excluding participants with gas kitchens, incremental influence due to cigarette smoking was detected. The 7-day, 3-room average level of NO₂ in the homes of nonsmokers and smokers without gas-fired appliances was 12 and 15 μg/m³, respectively, in the summer. The corresponding winter values were 19 and 22 μg/m³. Furthermore, the individual levels of NO₂ in the homes of smokers were generally below both the adjacent outdoor level and the National Ambient Air Quality Standard limit for annual exposure.     

Development of a personal exposure monitor for two sizes of inhalable particulates

Measurement of personal exposure to ambient level particulate concentrations is often extremely difficult because of a lack of personal exposure monitors capable of collecting measurable quantities within a meaningful sampling period. A new personal exposure monitor for two fractions of inhalable particulates (i.e., the 3–15 μm aerodynamic diameter and the < 3 μm or respirable fraction) has been developed and characterized. This monitor is capable of collecting a sample of each fraction that is quantifiable with ambient concentrations of inhalable/respirable particulates as low as 25 μg/m³ in a 24-h sampling period. Wind tunnel tests have been made on the particulate personal exposure monitor to determine sampling efficiency as a function of relative wind speed and orientation with respect to the sampler.     

Odor-annoyance estimates from roadtraffic combustion exhausts: Calibration with master scaling using pyridine as a reference

The present field study addressed the need for a procedure that provides a defined unit of measurement of perceived annoyance from environmental odors, calibrating the estimates for individual scaling behavior and context effects. In including 25 subjects, the purpose was to demonstrate the applicability of the master-scale procedure with magnitude estimation to perform such a calibration of odor-annoyance estimates for target stimuli such as road-traffic combustion exhausts (13 000 vehicles/d; averaging 47 μg/m³ over the day/night with peaks exceeding 100 μg/m³ of nitrogen dioxide; NO₂). For comparison, calibrated estimates were also obtained for a backyard expected to be considerably less polluted (comparable with 18 μg/m³ of NO₂) and for blank stimuli presented indoors. The data transformation for the calibration procedure with which annoyance is expressed in either master-scale units or pyridine equivalents requires estimates of a reference stimulus for which seven concentrations of pyridine were used. The results provide an illustration of master scaling of odor annoyance, and imply that use of a modulus (standard stimulus with a predefined annoyance magnitude), in contrast to master scaling, is not sufficient for calibration for individual scaling behavior and context effects.     

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.     

Introduction to and experimental conditions during the first year of the GMR chronic inhalation studies of diesel exhaust

A chronic exposure study was initiated to determine the effects of diesel exhaust on the health of experimental animals. For this purpose, test atmospheres of clean air (control) or freshly diluted diesel exhaust at concentrations of 250, 750, and 1500 μg/m³ were supplied to four 12.6 m³ inhalation chambers which housed rats and guinea pigs. Diesel aerosol size and concentration, as well as chamber temperature and relative humidity, were continually monitored and controlled to maintain the exposure dose levels and an environment of 22±2°C and 50%±20% relative humidity. The concentrations of CO and NO_x were found to be 5.8±1.0 mg/m³ and 7.9±1.0 mg/m³ above ambient in the chamber containing 1500 μg/m³ of particulate. Animals were supplied from the chambers, on a random basis, for both intramural and extramural studies throughout the exposure period. The experiment ran uninterrupted for over twelve months with mean diesel particle mass concentrations within 2% of the target values.     

Spatial distribution of uranium and thorium in the surface soil around proposed uranium mining site at Lambapur and its vertical profile in the Nagarjuna Sagar Dam

The understanding and evaluation of the possible interactions of various naturally occurring radionuclides in the world's third largest man-made dam, Nagarjuna Sagar located in Andhra Pradesh, India and built on river Krishna assumed significance with the finding of uranium deposits in locations near the dam. For the present work, surface soil samples from the mineralized area of Lambapur, Mallapuram, Peddagattu and sediment core samples from the Nagarjuna Sagar dam were analyzed for naturally occurring radionuclides namely uranium and thorium using gamma spectrometric technique. Also toxic elements lead and chromium were analysed by the Energy Dispersive X-ray Fluorescence Spectrometer (EDXRF) technique. Surface soil samples show a variation from 25 to 291 Bq/kg (2.02–23.5 mg/kg) for ²³⁸U and 32–311 Bq/kg (7.9–76.9 mg/kg) for ²³²Th. U/Th concentration ratio in surface soil samples ranged from 0.19 to 0.31 and was found comparable with the nation wise average of 0.26. The study of sediment core samples reflected higher U/Th concentration ratio of 0.30–0.33 in the bottom section of the core as compared to 0.22–0.25 in the upper section. The concentration ratio in the upper section of the core was similar to the ratio 0.23 found in the western Deccan Basalt region through which the river originates. A higher concentration of lead and chromium was observed in the upper section of the core compared to bottom section indicating the impact of river input on the geochemical character of dam sediment.     

Long-term effects of elemental composition of particulate matter on inflammatory blood markers in European cohorts

BackgroundEpidemiological studies have associated long-term exposure to ambient particulate matter with increased mortality from cardiovascular and respiratory disorders. Systemic inflammation is a plausible biological mechanism behind this association. However, it is unclear how the chemical composition of PM affects inflammatory responses.ObjectivesTo investigate the association between long-term exposure to elemental components of PM and the inflammatory blood markers high-sensitivity C-reactive protein (hsCRP) and fibrinogen as part of the European ESCAPE and TRANSPHORM multi-center projects.MethodsIn total, 21,558 hsCRP measurements and 17,428 fibrinogen measurements from cross-sections of five and four cohort studies were available, respectively. Residential long-term concentrations of particulate matter < 10 μm (PM₁₀) and < 2.5 μm (PM_2.5) in diameter and selected elemental components (copper, iron, potassium, nickel, sulfur, silicon, vanadium, zinc) were estimated based on land-use regression models. Associations between components and inflammatory markers were estimated using linear regression models for each cohort separately. Cohort-specific results were combined using random effects meta-analysis. As a sensitivity analysis the models were additionally adjusted for PM mass.ResultsA 5 ng/m³ increase in PM_2.5 copper and a 500 ng/m³ increase in PM₁₀ iron were associated with a 6.3% [0.7; 12.3%] and 3.6% [0.3; 7.1%] increase in hsCRP, respectively. These associations between components and fibrinogen were slightly weaker. A 10 ng/m³ increase in PM_2.5 zinc was associated with a 1.2% [0.1; 2.4%] increase in fibrinogen; confidence intervals widened when additionally adjusting for PM_2.5.ConclusionsLong-term exposure to transition metals within ambient particulate matter, originating from traffic and industry, may be related to chronic systemic inflammation providing a link to long-term health effects of particulate matter.