Lead and cadmium in urban allotment and garden soils and vegetables in the United Kingdom

In order to assess the intake of lead and cadmium by consumers of home grown vegetables in urban areas, replicated experimental plots of uniform size, comprising summer and winter crops, were established in 94 gardens and allotments in nine towns and cities in England.The geometric mean lead and cadmium concentrations for the soils (n = 94) were 217 g g^–1 (ranging from 27 to 1,676 g g^–1) and 0.53 g g^–1 (<0.2–5.9 g g^–1), respectively. Compared with agricultural soils, the garden and allotment soils contained elevated levels of lead but not cadmium.Lead concentrations in the vegetables ranged from <0.25 g g^–1 to 16.7 g g^–1 dry weight and cadmium concentrations ranged from <0.025 g g^–1 to 10.4 g g^–1 dry weight. Lead concentrations were higher than reported background levels, although <1% exceeded the statutory limit for saleable food in the UK (1 g g^–1 fresh weight). Cadmium concentrations were generally similar to background levels.     

Temporal variation and distribution of trace metals in freshwater and fish from Calabar River, S.E. Nigeria

An investigation on the abundance and distribution of trace metals (Fe, Cu, Zn, Mn, Cr, Cd and Pb) in water, and nine species of fish samples from Calabar river was carried out in 1992. The concentrations of iron (6000–7240gl^–1), zinc (4910–7230gl^–1), and cadmium (3–7gl^–1) showed moderate pollution while those of copper (420–630gl^–1), manganese (23–48gl^–1), chromium (<10–20gl^–1) and lead (<1–10gl^–1) in water were well below WHO permissible levels. Significant seasonal changes (0.001p0.25) were obtained for iron, copper, zinc, manganese and cadmium in water. Furthermore, iron, zinc and cadmium showed statistically significant spatial changes (0.005p0.10). Of the nine fish species studied, no statistically significant relationship between body weight and the concentrations of the metals was observed. The concentrations of the metals per mean total body weight apparently decreases in the order Fe>Zn>Cu>Mn>Pb>Cd=Cr and were within the limits that were safe for consumption.     

Soil Lead at Elementary Public Schools: Comparison Between School Properties and Residential Neighbourhoods of New Orleans

Soil studies, conducted in Maryland, Minnesota and Louisiana, have described the urban pattern of lead contamination. They have shown that the highest amounts of lead cluster within the interior of the largest cities. The results of the New Orleans urban patterns of distribution of soil lead provided the basis for further study. The hypothesis was tested that elementary school properties have the same pattern of soil lead contamination as their neighbouring residential communities. Thirty New Orleans Public Elementary Schools were selected for this study. Surface samples (2.5cm or 1 inch depth) were collected from playgrounds and next to entrances of each school. Results showed that soil lead on school properties follows the same relative contamination patterns (pvalue10^–5) as soil lead on residential properties of neighbouring communities. Schools however, have significantly lower lead contamination than the neighbouring residential properties. Innercity school properties present a higher risk of soil lead exposure than mid and outercity schools. Soils next to innercity school entrances showed the highest lead, with 18.5% having concentrations over 400gg^–1. Systematic landscaping around the school entrances would significantly reduce the hazard from lead dust contaminated soils.     

Lead exposure in Saudi Arabia from the use of traditional cosmetics and medical remedies

Twenty Henna samples were collected and analysed for lead by electrothermal atomic absorption spectrophotometry after a microwave acid digestion procedure. The mean lead concentration was 5.50 g g^–1, with a range from 1.29 g g^–1 to 16.48 g g^–1. The data did not show a high concentration of lead in these samples. However, if we take into account the popular use of henna, the cumulative effects of prolonged exposure to low lead especially in children cannot be ruled out.     

Effect of heavy metals (Zn,Hg, Cu,Cd, Pb,Ni) on the length growth of Mytilus edulis

The shortterm (10–22 d) effect of Zn, Hg, Cu, Cd, Pb, and Ni on the length growth of Mytilus edulis is studied. Significant reductions of growth rate was found at 0.3 g Hgl^-1, 3 g Cul^-1, 10 g Znl^-1, and 10 g Cdl^-1 added to the local sea water, while concentrations of up to 200 gl^-1 of Pb and Ni had no effect on the growth. With exposure to Cu and Zn, there was a linear reduction in growth rate with increasing metal concentration up to about 6 g Cul^-1 and 100 g Znl^-1. Above these levels, growth stopped with Cu, while with Zn it was stabilized at about 20% of control growth. When Hg and Cd were added, a curvilinear relationship between growth and metal concentration is indicated. With Hg, growth rate is nearly zero above 3–4 g Hgl^-1, while the growth rate was 50% of control after 10 d of exposure to 100 g Cdl^-1. At 2 g Cdl^-1 there was a significant stimulation of length increase. Observed EC₅₀-values for growth were 0.3–0.4 g Hgl^-1, 3–4 g Cul^-1, 60 g Znl^-1, and 100 g Cdl^-1.     

Environmental Accumulation of Airborne Fluorides in Romania

The nature and extent of pollution from an aluminium smelter and a fertiliser factory in Romania were studied. These are large industrial complexes, and both types of industry are known to release fluorides into the atmosphere. In grass samples collected from around the aluminium smelter, the maximum fluoride levels were found to be 4023mgkg^–1 and 162mgkg^–1 in unwashed and washed grass samples respectively, and 89mgkg^–1 in soils. For the fertiliser factory, the maximum levels in washed grasses were found to be 207mgkg^–1, and 11mgkg^–1 in the soils. In both locations, these maximum values were obtained in samples collected from within 200m of the factory limits, and compare with regional background levels of less than 10mgkg^–1 for grasses and 2mgkg^–1 for soils. The high fluoride levels of fluoride in the grasses are sufficient to give cause for concern for the effects that these could have on the local population and on grazing animals.     

Feeding,growth and bioluminescence of the heterotrophic dinoflagellate Protoperidinium huberi

Feeding, growth and bioluminescence of the thecate heterotrophic dinoflagellate Protoperidinium huberi were measured as a function of food concentration for laboratory cultures grown on the diatom Ditylum brightwellii. Ingestion of food increased with food concentration. Maximum ingestion rates were measured at food concentrations of 600 g C l^-1 and were 0.7 g C individual^-1 h^-1 (1.8 D. brightwelli cells individual^-1 h^-1). Clearance rates decreased asymptotically with increasing food concentration. Maximum clearance rates at low food concentration were ca. 23 l ind^-1 h^-1, which corresponds to a volume-specific clearance rate of 5.9x10⁵ h^-1. Cell size of P huberi was highly variable, with a mean diameter of 42 m, but no clear relationship between cell size and food concentration was evident. Specific growth rates increased with food concentration until maximum growth rates of 0.7 d^-1 were reached at a food concentration of 400 g C l^-1 (1000 cells ml^-1). Food concentrations as low as 10 g C l^-1 of D. brightwellii (25 cells ml^-1) were able to support growth of P. huberi. The bioluminescence of P. huberi varied with its nutritional condition and growth rate. Cells held without food lost their bioluminescence capacity in a matter of days. P. huberi raised at different food concentrations showed increased bioluminescence capacity, up to food concentration that supported maximum growth rates. The bioluminescence of P. huberi varied over a diel cycle, and these rhythmic changes persisted during 48 h of continuous darkness, indicating that the rhythm was under endogenous control.     

Background levels of soil beryllium in several countries

Beryllium and aluminium contents in uncontaminated soils from six countries are reported. The means and ranges of beryllium in the surface soils were as follows: 1.43(0.20–5.50)g g^–1 in Thailand (n=28), 0.7 (0.31–1.03) g g^–1 in Indonesia (n=12), 0.99(0.82–1.32) g g^–1 in New Zealand (n=3), 0.58(0.08-1.68)g g^–1 in Brazil (n=16), 3.52(2.49–4.97)g g^–1 in the former Yugoslavia (n=10), and 1.56(1.01–2.73) g g^–1 in the former USSR (n=8). The mean and range of beryllium contents of the surface soils in Japan (1.17(0.27–1.95)g g^–1 n=27) are situated within the values of the soils from these countries except for the Yugoslav soils derived from limestones. The mean of the mean beryllium contents of the surface soils in all these countries is 1.42 g g^–1 which will be used as a tentative average content of beryllium in uncontaminated surface soils, except for the soils derived from parent materials high in beryllium content. The beryllium contents of the subsoils were higher than those of the surface soils in New Zealand and Yugoslavia as is the case with Japan. The correlation coefficient between the contents of beryllium and aluminium in all the soil samples (n=113) including surface soils and subsoils was 0.505 (p < 0.001).     

Environmental Geochemistry of Soils and Waters of Susaki Area, Korinthos, Greece

Soil and water samples were collected from the Susaki area of Korinthos and analysed for heavy metals in order to evaluate their environmental impact. The geology of the studied area includes ultrabasic rocks and Neogene and Quaternary deposits whereas magnesite veins are found within the ultrabasic rocks. In the north part of the studied area post volcanic emissions of H₂S, CO₂ and H₂O vapor continue to the present day. All the samples were analysed for heavy metals by the ICP method. The element ranges (in g g^–1) for soil samples are: Cu 11–63, Pb 5–256, Zn 21–604, Ni 183–2665, Co 12–124, Mn 456–1434, As 5–104, Sr 44–730, V 21–84, Cr 163–2346, Ba 48–218, Zr 3–41, Y 3–13. The metals Pb, Zn, Ni, Co, Cr, Fe, Cu, Mn, As and Sr are enriched in the Susaki soils. The element ranges for water samples are: Cu 65–103ppb, Pb<10ppb, Zn<5ppb, Ni 21–163ppb, Co 2–12ppb, As<30ppb, Cr<20ppb, Ba 36–785ppb, Sb<10ppb, W<10ppb, Bi<30ppb, Mn 0.0–0.9 g g^–1, Fe 0.01–0.22 g g^–1, Na 843–3076 g g^–1, K 98–278 g g^–1, Si 39–65 g g^–1, P 0.1–0.2 g g^–1. There is a natural pollution of soils with elevated concentrations of Ni, Co, Mn, Fe and Cr due to the presence of ultrabasic rocks. Another natural case of As pollution of soils is due to the volcanic activity and the geothermal field in the area. The geochemical data of ground waters and also the ¹⁸, D data showed a mixing in different proportions between sea water and meteoric water.     

Stable lead isotope profiles in smelter and general urban communities: a comparison of environmental and blood measures

High-precision lead isotope ratios and lead concentrations have been compared statistically and graphically in women of child-bearing age (n = 77) from two smelter communities and one general urban community to evaluate the relative contributions to blood lead of tissue lead stores and lead from the contemporaneous environment (soil, floor dust, indoor airborne dust, water, food). Blood lead (PbB) contents were generally low (e.g. <10 g dL^–1). Statistically significant isotopic differences in blood and environmental samples were observed between the three cities although isotopic differences in blood for individual subjects living in close proximity (200 m radius) was as large as the differences within a city. No single environmental measure dominated the biological isotope profile and in many cases the low levels of blood lead meant that their isotopic profiles could be easily perturbed by relatively small changes of environmental exposure. Apportioning of sources using lead isotopes is possibly not feasible, nor cost effective, when blood lead levels are <5 g dL^–1. Interpretations based on statistical analyses of city-wide data do not give the same conclusions as when the houses are considered individually. Aggregating data from multiple subjects in a study such as this obscures potentially useful information. Most of the measures employed in this study, and many other similar studies, are markers of only short-to-medium integration of lead exposure. Serial sampling of blood and longer sampling times, especially for household variables, should provide more meaningful information.     

Thallium in marine plankton

Concentrations of thallium in phytoplankton (0.02 to 0.8 g g^–1), zooplankton (0.03 to 0.5 g g^–1) and ichthyoplankton (0.1 g g^–1) from the central Pacific were comparable , as were the atomic ratios of thallium to calcium (3x10^–6) and to potassium (1x10^–6) in those organisms. These relatively constant ratios, plus the biounlimited ocean profile of thallium, indicate that it is rapidly cycled through plankton in the same manner as potassium, its principal biogeochemical analogue. The higher atomic ratios of thallium to potassium in pelagic clays (6x10^–6) and ferromanganese nodules (4x10^–3) suggest that both biological transport processes and abiotic transport processes influence this trace element's oceanic cycle.     

Geochemistry of an arsenic anomaly in St. Elizabeth, Jamaica

A soil arsenic anomaly with concentrations up to 400g As g^–1 was discovered near Maggotty, St. Elizabeth, during an islandwide geochemical survey of Jamaica. Detailed sampling and chemical analysis of soil samples confirmed the arsenic levels and led to a better definition of the size of the anomaly. The area exceeding the 95th percentile (>65g As g^–1) of the islandwide concentrations has been determined to be at least 10km². The anomalous values may be the result of an ancient hot spring environment which was responsible for the introduction and deposition of Fe–As–S as pyrite and arsenopyrite in the limestone bedrock, which were subsequently oxidised and weathered to yield the arsenic rich soils. These soils were also enhanced in elements such as Sb, Fe and Co. Despite the high soil arsenic content, the arsenic concentration in the surface water is low and there seems to be no immediate health risk to the residents. The area, however, does present a potential hazard with changing land use.     

Effects of light intensity on nitrate and nitrite uptake and excretion by Chaetoceros curvisetus

Michaelis-Menten uptake kinetics were observed at all light intensities. With constant illumination, the V_max and K₁ in nitrate uptake over the natural light intensity range of 0 to 2000 E were 0.343 g-at NO₃–N(g)^-1 at protein-N h^-1 and 26 E, respectively. Nitrate uptake was inhibited at higher light intensities. The K_s for nitrate uptake did not vary as a function of light intensity remaining relatively constant at 0.62 g-at NO₃–N 1^-1. With intermittent illumination, the V_mzx for light intensity in nitrate uptake over a light intensity range of 0 to 5000 E was 0.341 g-at NO₃–N(g)^-1-at protein-N h^-1. No inhibition of nitrate uptake was observed at higher than natural light intensities. Chaetoceros curvisetus will probably never experience light inhibition of nitrate uptake under natural conditions.     

Particulate organic carbon and nitrogen in the adjacent seas of the Pacific Ocean

Particulate organic carbon (POC) and nitrogen in sea water were measured in samples collected in the adjacent seas of the Pacific Ocean during the cruises of T. S. Oshoro-Maru (1969, 1970) and the R. V. Hakuho-Maru (KH-70-4, KH-72-1). High values were obtained in the northern North Pacific and the Bering Sea, the concentration of particulate carbon in the upper 50-m layer ranged from 35 to 550 g Cl^-1. In the deep waters of these area, values above 50 g Cl^-1 were frequently observed. The lowest values in the surface layer and deeper layers were obtained in the Japan Sea (23 gCl^-1) and in the South China Sea (7 g Cl^-1) respectively. A consistent minimum was located in the intermediate waters (100–400 m) throughout the entire region studied. Variation with depth was generally irregular with marked peak values in different layers. The POC distribution consited of these peak values and a relatively uniform background concentration. These background values slightly decreased with increasing depth and were different locally. Correlation analysis between carbon concentration and apparent oxygen utilization (AOU) of ambient water for the samples in the Japan Sea and the Sulu Sea showed that there was no systematic decrease of particulate carbon with increasing AOU. In these areas, the carbon concentration scattered in the higher AOU domain ranged from 10–100 g Cl^-1. These observations support the conception that downward transport of particulate matter from the overlying surface layer in the adjacent seas of the Pacific Ocean may be fairly rapid.     

A role forAmanita muscaria L. in the circulation of cadmium and vanadium in a non-polluted woodland

The sporophore of the fungusAmanita muscaria L. contains greatiy elevated levels of cadmium (29.9 g g^–1 dwt) and vanadium (344.9 g g^–1 dwt) in comparison with the soil in a birch woodland (total (HNO₃-extractabie Cd 0.4 g g^–1 dwt, V 11.7 g g^–1 dwt). The significance of this remarkable concentration of normally rare and dispersed elements in terms of their circulation in the woodland has been investigated. Both elements are released from sporophore tissue in a form which can be taken up by a test plant (lettuce), cultivated in the woodland soil amended with different quantities of sporophore tissue, Cadmium levels in all plant tissues were elevated in comparison to the non-amended controls; only root vanadium levels responded to the amendment of the soil. The results are discussed in terms of their significance for the natural cycling of both elements. It is calculated that an abundant population of sporophores could circulate 1.4% of the total cadmium and 0.65% of the total vanadium pool found in the litter layer and 0–5 cm soil horizon in the sampled woodland over a period of 14 days (mean life span of a sporophore).     

Lead Contamination of Topsoil and Vegetation in the Vicinity of a Battery Factory in Nigeria

Levels of Pb, Zn, Cu, Cr, Ni and Cd were determined in topsoil and vegetation in the vicinity of a factory manufacturing lead- batteries in Ibadan, Nigeria. The samples were collected along five transects in different directions, and varying distances up to 1000m from the factory. Soil lead levels were found to be elevated around the factory, with average levels of about 2000mgkg^–1 close to the fence that declined gradually to about 50mgkg^–1 some 750m away. Soil-lead level around a primary school located about 500m from the factory was as high as 1450mgkg^–1. Lead levels were equally elevated in the vegetation, though average levels in vegetation were slightly lower than in the soil. Cadmium concentrations in soil and vegetation, though low, were more positively correlated with lead levels than any of the other metals are with lead.     

Lead in New Orleans soils: New images of an urban environment

This paper describes a survey of lead in soil and computer generated maps that have been derived for New Orleans, Louisiana. The soil survey included streetside, houseside and open space samples. Because the survey covered every census tract in the metropolitan area it was possible to construct a computer-generated map of the distribution of lead dust in the soils of the urban environment. The data base consists of coordinates, site characteristics and lead analytical results of 3,704 soil samples. The resulting graphics show peaks of lead ranging from 600–1,200 g per g in the streetside soil of the inner-city and a steeply declining slope to the suburban areas of the city where the lead content of streetside soils is less than 75 g/g. In the inner-city, the amount of lead in soils found near building foundations is 10 to 20 times higher than the soils adjacent to streets where the median lead content of soils is over 300 g g^–1. In areas surrounding the city core (mid-city), the amount of lead next to the foundation and adjacent to the street are equivalent with medians of 110 g g^–1. In suburban locations, the median lead content of soil along streetsides is 86 g g^–1. Soils adjacent to surburban foundations has a median Pb content of 50 g g^–1. The lowest median lead content in soil is found in open spaces, ranging from 212 to 40 to 28 g g^–1, respectively, for the inner-city, mid-city, and suburbs. These observations are consistent with the production and consumer use of lead-based paint and leaded-fuels within the modern city.     

Environmental Impacts of a Secondary Lead Smelter in Landskrona, Southern Sweden

Scandinavia has one secondary lead smelter that recycles lead from approximately 85% of used car batteries in Scandinavia and which has been active since the 1940s. The smelter, situated in Landskrona, has undergone a comprehensive clean up programme during the last decade, during which time production has doubled, while at the same time discharges of dust and lead to the atmosphere have decreased.Top and depth soil samples were taken on a 0.5km×0.5Km grid throughout the city of Landskrona, which covers an area of approximately 15km². Samples were analysed by ICPAES for a number of elements including Pb, Zn, Cu, Cd, As, Sb and Hg. Road dust samples from selected sites were collected and similarly analysed. Blood samples were taken from 37 volunteer schoolchildren (aged 8–11) from two schools in Landskrona. House dust samples were taken from each child's home. Soil samples were taken from homes which had gardens, public and school play areas. Elevated heavy metal concentrations were found in close proximity to the secondary lead smelter, and this soil enrichment influences the whole of the town, modified to some extent by the prevailing wind. The smelter does not influence the soil lead concentration at distances greater than 3.5km, where the soil reflects the background value for the area.Road dust samples also show decreases in lead concentrations with distance from the smelter. The average level of lead in house dust was considerably lower than that found in Birmingham, UK. Blood lead levels in the child population ranged from 1.5–5.1gdl^–1, with a mean of 3.05gdl^–1, showing a distinct decrease from those measured in 1978–82. No significant difference in blood lead concentrations with distance of the home from the smelter, nor between attenders at the two schools was revealed in the limited number of children studied.     

Indoor and outdoor household dust contamination in Cincinnati, Ohio, USA

Despite some progress in reducing the average lead level in the USA, the streets of Cincinnati, Ohio, are still contaminated by heavy metals. High levels of heavy metals will have significant unequivocal ecological impacts and pose a potential health hazard. This study evaluates the level of heavy- metal contamination in household dust and examines its relationships with the external environment. Samples of outdoor and indoor dust were collected from middle-income residential homes in the Greater Cincinnati Metropolitan District and the metal content was analysed by inductively coupled plasma atomic emission spectrophotometry. Results showed that the mean levels of lead in outdoor and indoor dusts are 650 g g-1 and 377 g g-1 and the copper levels are 253 g g-1 and 510 g g-1, respectively. The median levels are 156 g g-1 and 139 g g-1 for outdoor and indoor lead dusts and 35 g g-1 and 124 g g-1 for outdoor and indoor copper dusts. The degree of contamination may be ascribable to the age of the dwelling unit and the neighbourhood, the time when the unit was last painted, the presence of pets and the type of space heating. In addition, car exhausts seems to be a possible source of contamination.     

The relationship between surface dust lead loadings on carpets and the blood lead of young children

The final clean-up of residential lead abatement projects in federally-supported housing, as well as in other housing in a number of states, must meet surface dust lead clearance levels expressed as g of lead per square foot. These clearance levels were established because hand-to-mouth ingestion of lead-contaminated dust is recognised as a major pathway through which many children are exposed. A dilemma exists because many floors in housing undergoing abatement are carpeted and the established clearance levels are generally not recommended for use on carpets. These clearance levels are also used as 'action levels' to determine whether exposure reduction activities are needed. The US Environmental Protection Agency is currently in the process of issuing standards for hazardous levels of lead in interior dust and bare soil under Title X of the Housing and Community Development Act of 1992, The Residential Lead-Based Paint Hazard Reduction Act of 1992. An effort to develop a potential surface dust lead clearance level for carpets was made using an existing vacuum dust collection method that has previously been shown to be a reliable indicator of childhood lead exposure. This method was designed for use on carpeted and non-carpeted surfaces. Using data from the Cincinnati Soil Lead Abatement Demonstration Project, the suggested floor-dust lead level where an estimated 95% of the population of children would be expected to have blood lead values below the national goal of 10 g dL^–1, was more than an order of magnitude lower than the current floor-dust lead clearance level of 1080 g m^–2 (100 g ft^–2). Further comparisons of blood lead and carpet lead levels in other parts of the country should be performed before a risk-based lead loading clearance level is established.