Arsenic, cadmium, lead, copper and zinc in cattle from Galicia, NW Spain

Knowledge of trace and toxic metal concentrations in livestock is important for assessing the effects of pollutants on domestic animals and contaminant intakes by humans. Metal levels in cattle have been measured in various countries but not in Spain. In this study, the (wet wt.) concentrations of three toxic elements (arsenic, cadmium, lead) and two trace elements (copper, zinc) were quantified in the liver (Li), kidney (Ki), muscle (M) and blood (Bl) of calves (males and females between 6 and 10 months old) and cows (2-16 years old) from Galicia, NW Spain. For the toxic elements, geometric mean concentrations of arsenic in calves (sexes combined) and cows were 10.8 and 10.2 microg/kg (Li), 11.3 and 15.2 microg/kg (Ki), 3.75 and 4.25 microg/kg (M), 3.23 and 2.92 microg/l (Bl). The corresponding cadmium concentrations were 7.78 and 83.3 microg/kg (Li), 54.3 and 388 microg/kg (Ki), 0.839 and 0.944 microg/kg (M), 0.373 and 0.449 microg/l (Bl). Geometric mean concentrations of lead in calves and cows were similarly low and were 33.0 and 47.5 microg/kg (Li), 38.9 and 58.3 microg/kg (Ki), 6.37 and 12.5 microg/kg (M), 5.47 and 12.2 microg/l (Bl). Sex had almost no effect on the amount of toxic metal accumulated except that kidney cadmium concentrations were significantly higher in females than males. Age did influence accumulation; cadmium and lead (but not arsenic) concentrations in most tissues were significantly greater in cows than female calves. For the trace elements, geometric mean copper levels in calf and cow tissues were 49.9 and 36.6 mg/kg (Li), 4.27 and 3.63 mg/kg (Ki), 0.649 and 1.68 mg/kg (M) and 0.878 and 0.890 mg/l (Bl). The corresponding zinc concentrations were 46.3 and 52.5 mg/kg (Li), 14.2 and 20.7 mg/kg (Ki), 47.3 and 52.5 mg/kg (M) and 2.80 and 2.22 mg/l (Bl). Female calves had significantly higher levels than males of muscle zinc and blood copper and zinc. Female calves accumulated more copper but less zinc in the liver and kidneys compared with cows; this may have been associated with the chronic, low-level cadmium accumulation observed in cows. Overall, the levels of arsenic, cadmium, lead and zinc in cattle in Galicia do not constitute a risk for animal health. However, up to 20% of cattle in some regions in Galicia had levels of copper in the liver that exceeded 150 mg/kg wet wt. These animals may be at risk from copper poisoning.     

Effect of cadmium, lead and arsenic on the oviposition, hatching and embryonic survival of Biomphalaria glabrata

Biomphalaria glabrata is a widespread freshwater gastropod mollusc. The easy aquaculture of these organisms allow its use as an accessible tool for contamination bioassays. B. glabrata showed marked metabolic responses when exposed to cadmium, lead and arsenic. Those responses could also affect the reproduction of the snails. Taking into account this hypothesis, B. glabrata were exposed for 96 h (acute laboratory bioassays) to different concentrations of cadmium (0.1, 0.05 and 0 mg/L), lead (0.5, 0.1, 0.05 and 0 mg/L) and arsenic (0.5, 0.1, 0.05 and 0 mg/L). Snails were removed from the aquaria while eggs were left in the same contaminant concentrations. The effect of the assayed toxicants on snail reproduction was registered as the alterations of the total number of laid eggs (TNLE), hatching time and embryonic survival.At 0.10 mg/L cadmium significantly decreased the TNLE (p < 0.05) and no embryos survived. The lowest assayed level (0.05 mg/L) of cadmium, delayed the hatching time twice when it was compared with the control group (p < 0.01).Lead decreased the TNLE at 0.5 mg/L level (p < 0.01). The other assayed doses (0.05 and 0.10 mg/L) also decreased embryonic survival significantly (p < 0.05 and p < 0.01 respectively) and extended twice the time to hatching (p < 0.01). The 0.50 mg/L level killed all embryos.Arsenic at all studied concentrations decreased the TNLE (p < 0.05) while the hatching time was increased by 50%. Embryo survival only decreased at the highest level (0.5 mg/L) of arsenic assayed.In summary, the acute exposure (96 h) to cadmium lead and arsenic, altered the reproduction of B. glabrata, modifying the TNLE, hatching time and embryonic survival.     

Hepatic and renal concentrations of 10 trace elements in crocodiles (Crocodylus niloticus) in the Kafue and Luangwa rivers in Zambia

Hepatic and renal concentrations of the elements arsenic, cadmium, cobalt, copper, lead, manganese, mercury, molybdenum, selenium and zinc were determined in samples collected from four crocodiles from the Kafue River, Kafue National Park and five crocodiles from the Luangwa River, Luangwa National Park, Zambia. The concentrations of the essential elements were similar to those reported in other vertebrates. Arsenic and cadmium concentrations were low (medians below 0.05 microg As/g and below 0.16 microg Cd/g, wet wt.). Mercury and lead concentrations were several orders of magnitude higher (medians up to 3.7 microg Hg/g, and up to 8.7 microg Pb/g, all wet wt.) than in hippopotami from the same rivers, probably as a result of food-chain biomagnification. Judging by the results obtained in this study, pollution from the mining activity around the Kafue River drainage area in the Copperbelt region has not significantly influenced the trace element concentrations in tissues of the crocodiles in the Kafue National Park. The trace element concentrations measured may serve as reference values in future studies on crocodilians.     

Characterization of roadway stormwater system residuals for reuse and disposal options

The chemical characterization of sediments accumulated in catch basins and stormwater ponds provides important information for assessing risks associated with management of these residuals upon removal of accumulated deposits in stormwater systems. In this study, over a period of 15 months, more than 150 residual samples were collected from 77 catch basin units and 22 stormwater ponds from 16 municipalities throughout the state of Florida. Concentrations (mg/kg) of metals and metalloids (arsenic, barium, cadmium, chromium, copper, lead, mercury, nickel, selenium, silver, and zinc) and trace organics (volatile organics, semi-volatile organics, herbicides, and pesticides) in the sediments were measured. In addition, the synthetic precipitation leaching procedure (SPLP) was utilized to evaluate pollutant leachability risk for a subset of the samples collected. Measured pollutant concentrations were compared to corresponding risk-based guidelines in Florida (i.e., Florida soil cleanup target levels) to assess potential human health risks of beneficial use of these residuals through land application. Leached concentrations were compared to risk-based water quality guidelines (i.e., Florida groundwater cleanup target levels) to examine the potential for groundwater contamination. Although several metals (arsenic, barium, chromium, copper, nickel, lead, and zinc) were routinely detected in the catch basin and stormwater pond sediments, their concentrations were generally lower than the Florida's risk-based cleanup target levels for soils. A small number of organochlorine compounds (e.g., 4,4′-DDE, 4,4′-DDT) were detected, but only in a limited number of the samples (less than 10%); leaching of trace organic pollutants above the Florida risk-based groundwater thresholds was rare. The results suggest that when land-applied or beneficially used, these residuals are not expected to pose a significant threat to human health or the environment and the results of this research will provide stormwater managers and environmental management authorities with a useful resource to examine proper disposal and beneficial use of catch basin and stormwater pond sediments.     

Trace element and Sigma DDT concentrations in horticultural soils from the Tasman, Waikato and Auckland regions of New Zealand

The long-term routine use of agrichemicals can result in elevated levels of trace elements and persistent organic pollutants in soils. Trace element concentrations and SigmaDDT levels were measured in soil (0-7.5 cm) samples collected from horticultural and grazing properties in 3 regions of New Zealand (Auckland, Tasman and Waikato). Elevated levels of arsenic (<2 to 58 mg kg(-1)), cadmium (<0.1 to 1.5 mg kg(-1)), copper (5 to 523 mg kg(-1)), lead (5 to 243 mg kg(-1)) and SigmaDDT (<0.03 to 34.5 mg kg(-1)) were detected in soils from all 3 regions. With the exception of cadmium and zinc, significantly higher levels of contaminants were generally detected in horticultural soils than in grazing soils. Our results have implications for the on-going use of agrichemicals as concentrations of cadmium, copper, tin and zinc in some samples exceeded ecotoxicity based soil criteria. The p,p'-DDE:DDT ratios indicate that the degradation of DDT in NZ horticultural soils may be inhibited by the co-contamination with trace elements.     

Brominated flame retardants in Belgian home-produced eggs: levels and contamination sources

The extent and the sources of contamination with brominated flame retardants (BFRs), such as polybrominated diphenyl ethers (PBDEs) and hexabromocyclododecane (HBCD), in home-produced eggs from free-foraging chicken of Belgian private owners were investigated. Various factors, such as seasonal variability, exposure of chickens through diet (kitchen waste) and soil, and elimination of BFRs through eggs and faeces were assessed. PBDEs were more important than HBCD in terms of concentrations and detection frequency. Concentrations of PBDEs and HBCD in Belgian home-produced eggs were relatively low and comparable with reported levels from other European countries and the US. The concentrations of PBDEs (sum of 13 congeners, including BDE 209) ranged between not detected and 32 ng/g lipid weight (lw), with medians of 3.0 and < 2.0 ng/g lw for the autumn 2006 and spring 2007 campaigns, respectively. When present, BDE 209 was the major PBDE congener (45% of sum PBDEs). When BDE 209 was not detected, the PBDE profile was composed of PentaBDE (BDE 99 and BDE 47), with, in some cases, higher contribution of OctaBDE (BDE 183 and BDE 153). HBCD was also detected (< 0.4 and 2.9 ng/g lw for the autumn 2006 and spring 2007 campaigns, respectively), but at lower detection frequency. The highest HBCD value was 62 ng/g lw. The similarity between profiles and seasonal variations in the concentrations of BFRs in soil and eggs indicate that soil is an important source, but not the sole source, for eggs laid by free-foraging chicken. The contamination of eggs with PBDEs and HBCD appears to be of low concern for public health and the contribution of eggs to the total daily intake of PBDEs appears to be limited (10% for chicken owners and 5% for the average Belgian consumer).     

Elemental and iron isotopic composition of aerosols collected in a parking structure

The trace metal contents and iron isotope composition of size-resolved aerosols were determined in a parking structure in Tempe, AZ, USA. Particulate matter (PM) < 2.5 µm in diameter (the fine fraction) and PM > 2.5 µm were collected. Several air toxics (e.g., arsenic, cadmium, and antimony) were enriched above the crustal average, implicating automobiles as an important source. Extremely high levels of fine copper (up to 1000 ng m^− 3) were also observed in the parking garage, likely from brake wear. The iron isotope composition of the aerosols were found to be + 0.15 ± 0.03‰ and + 0.18 ± 0.03‰ for the PM < 2.5 µm and PM > 2.5 µm fractions, respectively. The similarity of isotope composition indicates a common source for each size fraction. To better understand the source of iron in the parking garage, the elemental composition in four brake pads (two semi-metallic and two ceramic), two tire tread samples, and two waste oil samples were determined. Striking differences in the metallic and ceramic brake pads were observed. The ceramic brake pads contained 10-20% copper by mass, while the metallic brake pads contained about 70% iron, with very little copper. Both waste oil samples contained significant amounts of calcium, phosphorous, and zinc, consistent with the composition of some engine oil additives. Differences in iron isotope composition were observed between the source materials; most notably between the tire tread (average = + 0.02‰) and the ceramic brake linings (average = + 0.65‰). Differences in isotopic composition were also observed between the metallic (average = + 0.18‰) and ceramic brake pads, implying that iron isotope composition may be used to resolve these sources. The iron isotope composition of the metallic brake pads was found to be identical to the aerosols, implying that brake dust is the dominant source of iron in a parking garage.     

Trace element deposition and trends during a ten year period in Finland

The deposition of aluminium, arsenic, cadmium, chromium, copper, iron, lead, manganese, nickel, vanadium and zinc in bulk precipitation was examined at eight background stations in Finland during the last 10 years (1998-2007). The annual deposition was from the lowest values to the highest Cd < As < Cr < Ni < V < Cu and Pb < Mn < Zn < Al < Fe. Most of the elements had a south to north decreasing gradient mainly due to minor domestic emissions in the north, growing distance to the large European source areas and differences in the length of snow-cover period. Element enrichment factors divided the trace elements to the following categories: (1) slightly enriched Cr, Fe and Mn; (2) moderately enriched Cu, Ni and V; and (3) highly enriched As, Cd, Pb and Zn. Trend analysis of annual depositions showed that the established decreasing trend in As and Pb deposition continued during our study period while Cr, Cu and Fe depositions have lately increased. No statistically significant trends were detected for Cd, Mn, Ni, V and Zn during the studied years. Additionally, the measurement uncertainty of trace elements was evaluated for the whole measurement chain.     

Milk trace elements in lactating cows environmentally exposed to higher level of lead and cadmium around different industrial units

The present investigation was carried out to assess the trace mineral profile of milk from lactating cows reared around different industrial units and to examine the effect of blood and milk concentration of lead and cadmium on copper, cobalt, zinc and iron levels in milk. Respective blood and milk samples were collected from a total of 201 apparently healthy lactating cows above 3 years of age including 52 cows reared in areas supposed to be free from pollution. The highest milk lead (0.85 ± 0.11 µg/ml) and cadmium (0.23 ± 0.02 µg/ml) levels were recorded in lactating cows reared around lead–zinc smelter and steel manufacturing plant, respectively. Significantly (P < 0.05) higher concentration of milk copper, cobalt, zinc and iron compared to control animals was recorded in cows around closed lead cum operational zinc smelter. Analysis of correlation between lead and other trace elements in milk from lactating cows with the blood lead level > 0.20 µg/ml (n = 79) revealed a significant negative correlations between milk iron and milk lead (r = − 0.273, P = 0.015). However, such trend was not recorded with blood lead level < 0.20 µg/ml (n = 122). The milk cobalt concentration was significantly correlated (r = 0.365, P < 0.001) with cadmium level in milk and the highest milk cadmium (> 0.10 to 0.39 µg/ml) group had significantly (P < 0.05) increased milk cobalt. It is concluded that increased blood and milk lead or cadmium level as a result of natural exposure of lactating cows to these environmental toxicants significantly influences trace minerals composition of milk and such alterations affect the milk quality and nutritional values.     

Size distribution and chemical composition of airborne particles in south-eastern Finland during different seasons and wildfire episodes in 2006

The inorganic main elements, trace elements and PAHs were determined from selected PM₁, PM_2.5 and PM₁₀ samples collected at the Nordic background station in Virolahti during different seasons and during the wildfire episodes in 2006. Submicron particles are those most harmful to human beings, as they are able to penetrate deep into the human respiratory system and may cause severe health effects. About 70-80%, of the toxic trace elements, like lead, cadmium, arsenic and nickel, as well as PAH compounds, were found in particles smaller than 1 µm. Furthermore, the main part of the copper, zinc, and vanadium was associated with submicron particles. In practice, all the PAHs found in PM₁₀ were actually in PM_2.5. For PAHs and trace elements, it is more beneficial to analyse the PM_2.5 or even the PM₁ fraction instead of PM₁₀, because exclusion of the large particles reduces the need for sample cleaning to minimize the matrix effects during the analysis. During the wildfire episodes, the concentrations of particles smaller than 2.5 µm, as well as those of submicron particles, increased, and also the ratio PM₁/PM₁₀ increased to about 50%. On the fire days, the mean potassium concentration was higher in all particle fractions, but ammonium and nitrate concentrations rose only in particles smaller than 1.0 µm. PAH concentrations rose even to the same level as in winter.     

Distribution of 23 elements in the kidney,liver and lungs of workers from a smeltery and refinery in north Sweden exposed to a number of elements and of a control group

The levels of antimony, arsenic, cadmium, caesium, chromium, cobalt, copper, gold, iron, lanthanum, lead, manganese, mercury, molybdenum, phosphorus, rubidium, scandium, selenium, silver, tellurium, tin, tungsten and zinc in the kidney, liver and lungs of autopsy specimens from exposed workers in North Sweden, as well as from a control group, have been assayed quantitatively. The workers had been exposed to several elements and their compounds, e.g. lead, mercury, arsenic and cadmium, for long periods in arsenic, lead or selenium plants and in a lead or copper smelter.The chemical analysis was by neutron activation analysis and atomic absorption spectrophotometry.Median levels of antimony, arsenic, cadmium, chromium, cobalt, lanthanum, lead or selenium in kidney, liver or lungs in the exposed worker group were found to be about 2 to 16 times as great as the corresponding levels for the control group. Long biological half-life values were observed for these elements, especially in lung tissue.     

陶瓷地理标志产品微量元素迁移量检测研究

利用电感耦合等离子体质谱仪对20种陶瓷地理标志产品中的砷、镉、铬、镍、铅、锑、锌、铜、锰等9种微量元素迁移量情况进行检测。结果显示,镉、铬、锑在20种地理标志产品陶瓷中均未检出;铅、锌、铜、锰迁移量在有釉瓷（陶）器的多数种类中检出,其中锌迁移量突出;砷、镍迁移量在无釉陶器中检出。     

Effects of chloride,sulfate and natural organic matter (NOM) on the accumulation and release of trace-level inorganic contaminants from corroding iron

This study examined effects of varying levels of anions (chloride and sulfate) and natural organic matter (NOM) on iron release from and accumulation of inorganic contaminants in corrosion scales formed on iron coupons exposed to drinking water. Changes of concentrations of sulfate and chloride were observed to affect iron release and, in lesser extent, the retention of representative inorganic contaminants (vanadium, chromium, nickel, copper, zinc, arsenic, cadmium, lead and uranium); but, effects of NOM were more pronounced. DOC concentration of 1 mg/L caused iron release to increase, with average soluble and total iron concentrations being four and two times, respectively, higher than those in the absence of NOM. In the presence of NOM, the retention of inorganic contaminants by corrosion scales was reduced. This was especially prominent for lead, vanadium, chromium and copper whose retention by the scales decreased from >80% in the absence of NOM to <30% in its presence. Some of the contaminants, notably copper, chromium, zinc and nickel retained on the surface of iron coupons in the presence of DOC largely retained their mobility and were released readily when ambient water chemistry changed. Vanadium, arsenic, cadmium, lead and uranium retained by the scales were largely unsusceptible to changes of NOM and chloride levels. Modeling indicated that the observed effects were associated with the formation of metal–NOM complexes and effects of NOM on the sorption of the inorganic contaminants on solid phases that are typical for iron corrosion in drinking water.     

Heavy metal and arsenic content in seabirds affected by the Prestige oil spill on the Galician coast (NW Spain)

Seabirds are top consumers in marine foodchains which offer opportunities to detect and assess the toxicological effects of different inorganic elements on the marine ecosystem. In order to provide baseline data concerning trace element levels in seabird species from NW Spain, zinc, copper, arsenic, chromium, lead, cadmium and mercury concentrations were analyzed in liver of three different seabird species (common guillemot, Atlantic puffin and razorbill) affected by the Prestige oil spill in September 2002 on the Galician coast. In general, with the exception of mercury, levels of all the analyzed elements were similar or lower in comparison with those reported for the same species in other Atlantic areas, and did not exceed levels indicative of increased environmental exposure.     

A study of metal concentrations and metallothionein binding capacity in liver, kidney and brain tissues of three Arctic seal species

Arctic seals are known to accumulate relatively high concentrations of potential toxic heavy metals in their vital organs, such as livers and kidneys, as well as in their central nervous system. We therefore decided to determine whether mercury, copper, cadmium and zinc levels in liver, kidney and brain tissues of three Arctic seal species were associated with the intracellular metal-binding protein metallothionein (MT) as a sign of toxic exposure. Samples from four ringed (Phoca hispida), five harp (P.groenlandica) and five hooded (Cystophora cristata) seals taken during field trips to Central West Greenland (Godhavn) and the Barents Sea in the spring of 1999 were used for the present study. In all three seal species concentrations of mercury, zinc and copper were highest in the liver, except for cadmium which was highest in the kidneys. Metal concentrations increased significantly in the order: ringed seal < harp seal < hooded seal for both kidney and liver tissues. MT concentrations were highest in the kidneys and the concentrations increased in the order: ringed seal < hooded seal < harp seal. MT metal-binding capacity was highest in the kidneys for all three species and increased in the same order: ringed seals (2-10%) < hooded seals (8-15%) < harp seals (27-63%). We therefore suggest that there are species-specific differences in the sub-cellular handling of heavy metals which indicate differences in sensitivity and health implications. However, a larger sample size is needed in order to test the relationship between metal concentrations and MT up-regulation in order to decide which metals are the most important and to elucidate whether the MT binding capacity is sufficient to protect tissues (i.e. kidney) from metal toxicosis. MT with its binding capacity could be a useful marker for environmental exposure to metals and their potential toxicity in the Arctic.     

The determination of cadmium. lead, copper and zinc in ground water, estuarine water, sewage and sewage effluent by anodic stripping voltammetry

Anodic stripping voltammetry (ASV) using the thin-film mercury electrode was shown to be a successful technique for the determination of total (free plus complexed) trace metal concentrations in various types of aqueous sample. The method developed involved the minimum of sample treatment and required only simple and inexpensive equipment. The practical limit of sensitivity was about 0·1 μg I⁻¹ for cadmium, lead and copper. The determination of zinc was found to be complicated by the formation of an intermetallic compound with copper. Interference by other trace metals and by complexing agents was investigated. Photochemical oxidation for the decomposition of complexes of the metals with organic ligands in filtered sewage and sewage effluent was found to be successful, although the process is slower for cadmium than for the other metals. Good agreement with atomic absorption spectroscopy was obtained for all the types of aqueous sample investigated. Possible improvements of the ASV technique are discussed.     

Records and sources of metal pollutants in a dated Loch Lomond sediment core

Lead, zinc, copper, chromium, arsenic and cadmium were measured in a sediment core from southern Loch Lomond for which ²¹⁰Pb dating indicated a sedimentation rate of 22±2 mg/cm²/yr corresponding to a mean accumulation rate of 0.36 mm/yr.While copper and chromium were enriched to only a minor extent, the lead, zinc, arsenic and cadmium concentrations were markedly enhanced in upper sections. Increasing anthropogenic input associated with industrial activity centred on Glasgow seems responsible for the vertical distribution of lead, zinc and cadmium but a high 0–1 cm level of arsenic (474 μg/g), strongly correlated with enhanced iron content in the surface oxidising layer of sediment, appears attributable to post-depositional diagenetic mobilisation and upward migration in the reducing zone of the sediment column.Leaching, using CH₃CO₂H/NH₂OH·HCl, released over 90% and 80% of the common metal pollutants, lead and zinc, from surface sediment. Onset of an approximately tenfold increase in lead and zinc concentrations above “background” levels of 13±2 μg/g and 47±13 μg/g to upper section levels of 140–170 μg/g and 450–460 μg/g respectively was placed at late-18th century, in accord with the records of the commencement of significant industrial activity in the Glasgow area. Current anthropogenic fluxes (μg/cm² /yr) of lead (2.51±0.34) and zinc (8.84±1.20) to the sediment are in agreement with recent atmospheric deposition data for the adjoining Clyde Sea Area.The general concordance between anthropogenic metal fluxes to Loch Lomond sediment and atmospheric deposition fluxes endorses the potential usefulness of Loch Lomond sediment data to the resolution of pollution sources in the adjoining sea lochs and firth of the Clyde Sea Area, illustrated here through consideration of the comparative distribution of chromium in relation to its historical use.     

Reproductive toxicity of nitroaromatics to the cricket, Acheta domesticus

The effect of TNT (2,4,6-trinitrotoluene) and its metabolites, 2,4-dinitrotoluene (2,4-DNT), 2-amino-4,6-dinitrotoluene (2A-DNT), and 4-amino-2,6-dinitrotoluene (4A-DNT) on cricket (Acheta domesticus) reproduction was evaluated. We previously used crickets to assess the toxicity of a nitramine explosive (RDX) and its metabolites. It is common to find that while much information on the environmental impact of the parent compound is available in the literature, such is often not the case for the degradation metabolites of the parent compound. In some instances, these metabolites are as toxic (or more so) as the parent compound and we hypothesized that this might be the case for TNT. The presence of TNT and its metabolites in sand (10 µg/g) did not adversely affect cricket egg production, but adversely affected hatching of cricket eggs as compared to controls. However, there were no differences in hatching success among TNT and metabolite treatment groups. Hatching success of cricket eggs in soil or following topical exposure decreased as concentrations of TNT and its metabolites increased. The relative toxicity of TNT and its metabolites in soil generally followed the trend of TNT < 2A-DNT < 4A-DNT < 2,4-DNT. In addition, toxicity appeared to be higher in sand than in sandy loam soil or in the topical exposure test. After 45 days of exposure in sandy loam soil, the EC₂₀ (20% effect concentration), EC₅₀ (50% effect concentration), and EC₉₅ (95% effect concentration) were 14, 116, and 10,837 µg/g for TNT: 1.7, 32, and 16,711 µg/g for 2A-DNT: 1.9, 9, and 296 µg/g for 4A-DNT: and 0.4, 5.7, and 1437 µg/g for 2,4-DNT. Overall, results suggest that parent TNT and metabolites are toxic to cricket eggs at relatively high concentrations and these toxic effects are manifested as a decrease in hatching success.     

The association between low levels of lead in blood and occupational noise-induced hearing loss in steel workers

As the use of leaded gasoline has ceased in the last decade, background lead exposure has generally been reduced. The aim of this study was to examine the effect of low-level lead exposure on human hearing loss. This study was conducted in a steel plant and 412 workers were recruited from all over the plant. Personal information such as demographics and work history was obtained through a questionnaire. All subjects took part in an audiometric examination of hearing thresholds, for both ears, with air-conducted pure tones at frequencies of 500, 1000, 2000, 3000, 4000, 6000 and 8000 Hz. Subjects' blood samples were collected and analyzed for levels of manganese, copper, zinc, arsenic, cadmium and lead with inductive couple plasma-mass spectrometry. Meanwhile, noise levels in different working zones were determined using a sound level meter with A-weighting network. Only subjects with hearing loss difference of no more than 15 dB between both ears and had no congenital abnormalities were included in further data analysis. Lead was the only metal in blood found significantly correlated with hearing loss for most tested sound frequencies (p < 0.05 to p < 0.0001). After adjustment for age and noise level, the logistic regression model analysis indicated that elevated blood lead over 7 μg/dL was significantly associated with hearing loss at the sound frequencies of 3000 through 8000 Hz with odds ratios raging from 3.06 to 6.26 (p < 0.05 ~ p < 0.005). We concluded that elevated blood lead at level below 10 μg/dL might enhance the noise-induced hearing loss. Future research needs to further explore the detailed mechanism.     

The fate and transport of mercury, methylmercury, and other trace metals in Chesapeake Bay tributaries

Six tributaries to the Chesapeake Bay were analyzed for suspended particulate matter, dissolved organic carbon, particulate organic carbon, mercury, methylmercury, lead, nickel, zinc, cadmium, chromium, and copper. This study examined the importance of flow regime, suspended particulate concentration, and watershed characteristics on the transport of mercury, methylmercury, and other trace metals. Total mercury concentrations were higher under high flow conditions which is consistent with the tendency of this metal to bind strongly to particulate matter. Methylmercury showed less flow rate dependence. Nickel, lead, and zinc concentrations responded strongly to flow rate on the Potomac River, while weaker correlations were found on the other rivers sampled. Cadmium, copper, and chromium concentrations were the least influenced by flow. Partition coefficients calculated in this study were similar to those of other estuaries and overall decreased in the order of Hg > Ni-MMHg > Cr-Pb-Zn > Cd > Cu. Watershed yield estimates and associated retention factors were calculated for the various rivers. These calculations showed that for most of the rivers, mercury was the most strongly retained within the watershed.