Aqua regia extractable trace elements in surface soils of venezuela

Surface soils (0–15 cm) were sampled at 10–20 km intervals along two transects in Venezuela. One (1162 km, 70 samples) ran west to east parallel with the Caribbean coastline, the other (920 km, 92 samples) ran south to north from the frontier with Brazil to the Caribbean shore. Sampling took place in both a wet and a dry season. Trace metals were extracted from dried, sieved (<2 mm) soil with boiling aqua regia followed by analysis by ICP or flame AAS. Metal values did not differ significantly between the two seasons and dates were averaged. Geometric mean values for the west–east transect were: Cr=41.5, Cu 17.9, Cs 3.6, Li=13.9, Mn=294, Ni=21.3, Pb=17.4, Sr=39.4, V=60.4 and Zn = 83.7g g^–1, respectively. Similarly, for the south–north transect Cr=21.3, Cu=4.3, Cs=1.1, Li=2.0, Mn=55.7, Ni=4.4, Pb=6.1, Sr=13.3, V=28.2 and Zn=16.7g g^–1, respectively. A classification of samples by lithology showed surface soil composition to be related to rock composition. Metal values were low in the soils in the south of the country, in the Guyana highlands (Gran Sabana). Low Zn contents were prevalent. Lead contents were affected by roadside fallout from vehicles using leaded petrol except that high Pb contents of soils in the Gran Sabana were of more complex origin.     

Populational distribution I: The digital simulation

This paper presents a method of investigating the distributional pattern of a biological population, using a technique of simulation. The method consists of the comparison of the empirical frequency curve of a population, obtained using the Method of Quadrats, with a simulated one, since the pattern of the simulated curve depends on the simulated distribution. An example is given.     

The distribution of heavy metals in deposited urban dusts and sediments, Coventry, England

Samples of urban dusts and sediments have been collected and categorised into three compartment those which act mainly as sources, those undergoing transport and those which have been deposited. The sediments were fractionated into <63m to match similar sized lacustrine sediments and <2mm to represent natural and anthropogenic fluvially transported sediments. Preliminary results of total heavy metals analysis show that the <2mm fraction of the source group exhibits the greatest variabilty in metal concentrations. Overall, however, the <63m fraction dominates regardless of compartment. Some heavy metal concentrations decrease through the sourcetransportdeposit process, possibly due to selective onward transport of finer material or other anthropogenic processes unique to the urban environment (e.g. street cleansing). Sitespecificity is indicated in a comparison with other similar studies.     

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.     

Lead contamination in the roadside soils of Slovenia

The level of lead contamination along the roadway Ljubljana to Zagreb was established in 184 soil samples. The samples were taken from two depths (0–5cm and 15–20cm) and at different distances from the roadway. The influence of terrain morphology, prevailing winds, geological parent material and type of vegetation was estimated. Heavy traffic is confirmed as main source of lead contamination (average enrichment factor 17) in soils. The highest lead accumulation is localised in the top soil layer and within 10m from the roadside. Contamination with lead is more pronounced in soil samples from cuttings and slopes than in soils from plains and mounds. Soils derived from carbonate rocks contain higher lead concentration than those derived from other parent material.     

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.     

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.     

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.     

The lead content and isotopic composition of british coals and their implications for past and present releases of lead to the UK environment

More than 60 coal samples, predominantly from the principal coalfields of England and Wales (25) and Scotland (30), were analysed for lead by AAS and for stable lead isotopes by ICPMS. While the average lead content of Scottish coal, 23.9mg kg^–1, was more than double that of coal from England and Wales, 11.0mg kg^–1, the corresponding mean ²⁰⁶Pb/²⁰⁷Pb ratios (± 1 s.d.) were nearly identical, at 1.181±0.011 and 1.184±0.006, respectively. In the light of the lead isotopic signatures of British coals and of both indigenous (²⁰⁶Pb/²⁰⁷Pb 1.17) and imported Australian (²⁰⁶Pb/²⁰⁷Pb 1.04) lead ores, an approach based on estimated lead emissions from these sources and the deconvolution of the historical lead and ²⁰⁶Pb/²⁰⁷Pb records preserved in lake sediments, peat bogs and archival herbage material indicates that coal combustion became an increasingly significant contributor to atmospheric lead deposition in the UK during the period 1830–1930, especially after the onset of Englands decline as a major location of lead mining and smelting in the late19th Century. Since 1930 and the introduction of leaded petrol, the atmospheric ²⁰⁶Pb/²⁰⁷Pb ratio in the UK has been strongly influenced by carexhaust emissions of comparatively ²⁰⁶Pbdepleted lead of predominantly Australian origin, counterbalanced to some extent by coalcombustion emissions of lead, although these have fallen dramatically since the mid1950s. Nevertheless, with the introduction and substantial uptake of unleaded petrol in the UK during the last decade, even the declining releases from coal, along with contributions from other sources, are continuing to affect the atmospheric lead content and ²⁰⁶Pb/²⁰⁷Pb ratio.     

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.     

Evaluation of Public Housing Lead Risk Assessment Data

A unique data set from lead risk assessments performed on 67 public housing developments from across the United States was made available for analyzes. The data set includes results of lead analysis from 5906 dust wipes and from 1222 soil samples. A total of 487 dwelling units in these developments, as well as associated common areas, were sampled, all by the same team of inspectors. The number of dwelling units within a development that were sampled reflected the guidelines then in force, the 1990 Interim HUD Guidelines, rather than those specified in the 1995 Guidelines. Median dust lead loadings for floors, 151gm^–2 (14gft^–2), and window sills, 936gm^–2 (87gft^–2), were much less than former HUD limits of 1076gm^–2 (100gft^–2) and 5380gm^–2 (500gft^–2), respectively and are only about one-third of the recently established limits of 431gm^–2 (40gft^–2) and 2690gm^–2 (250gft^–2). In contrast, the median lead loading for window troughs, 8560gm^–2 (795gft^–2), was almost identical to the HUD clearance limit of 8610gm^–2 (800gft^–2). There was a strong positive correlation between floor and window trough lead loading values for samples from the same dwelling units and those from common areas of the housing developments. Door threshold samples, which may reflect conditions exterior to the dwelling unit, were collected from 53 dwelling units. Median lead loading levels of these samples were more than ten times higher than those in floor samples from the same dwelling units, were about the same as window sill samples and about one-half of levels in window trough samples. Composite sample results, simulated by averaging results from four samples within a dwelling unit, revealed that in order to have the same rate of excedence of standards, the composite standards would have to be reduced, for example, from the single sample value of 1076gm^–2 (100gft^–2) to 527gm^–2 (49gft^–2) for floor samples and from the single sample value of 8610gm^–2 (800gft^–2) to 5160gm^–2 (479gft^–2) for window troughs. For this public housing data set, the portion of the units in developments containing more than 225 units which exceeded the established limit for window samples was the same when using either the full data set or a random one-half of the data set. This suggests that, for this data set, the number of dwelling units sampled was excessive . Thus, the required increase in the number of dwelling units to be sampled specified in the 1995 Guidelines for developments with more than 225 dwelling units, may not have been necessary if this data set is representative of public housing developments in the United States.     

Effect of daylight variations on the energy budgets of shallow-water corals

Energy budgets were determined for small pieces (nubbins) of the coralsPocillopora damicornis, Montipora verrucosa andPorites lobata living at a water depth of 3 m on the fringing reef of Coconut Island, Kaneohe, Hawaii. The budgets were determined for three different types of day: an ideal day with no cloud and an in situ daily integrated irradiance at 3 m of 14.385 E m^–2 d^–1; a normal day with sporadic cloud cover and daily irradiance of 11.915 E m^–2 d^–1; and an overcast day with daily irradiance of 6.128 E m^–2 d^–1. On the ideal day, the energy fixed in photosynthesis was more than that required for respiration and growth of both zooxanthellae and animal components of the association, and there was a predicted loss of between 19.3 and 32.4% of the energy fixed. On a normal day, the total photosynthetic energy fixation was lower and the excess was between 12.1 and 27.9% of the energy fixed. On the overcast day, however, in bothPocillopora damicornis andPorites lobata energy expenditure exceeded photosynthetic energy fixation and the budget was in deficit. Estimates of rate of mucus secretion on an overcast day were derived and, when incorporated into the energy budget, it was predicted that all three species would have a deficit budget, necessitating the catabolism of lipid reserves. From published values for lipid storage in these species it was calculated that the reserves would last from 28 d inPocillopora damicornis to 114 d inM. verrucosa. A model is suggested in which corals draw upon their extensive lipid stores on days of sub-optimal light, replenishing the reserves again when daily light levels are high, and finally excreting the excess energy fixed, as mucus-lipid when the lipid stores are replete.     

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.     

Primary production in Dumbell Bay in the Arctic Ocean

Photosynthesis, chlorophyll, inorganic nutrients, and related factors were measured throughout a productive season in a small coastal inlet of the Arctic Ocean. Significant production was confined to 5 m for a very limited time period beacause of both light and nutrient limitations. Maximum chlorophyll was 8.2 mg Chl a m^-3 and maximum gross and net photosynthesis rates were 830 and 550 mg C m^-2 d^-1. Annual gross and net photosynthesis is estimated at about 12 and 9 g C m^-2 respectively. The effect of light stimulation on assimilation is described, sources of coastal zone nutrient enrichment are considered, and discrepancies between gross and net photosynthesis are discussed with reference to the growth characteristics of the phytoplankton population.Bigelow Laboratory for Ocean Sciences. Contribution No. 76008     

Sorption of the natural endocrine disruptors,oestrone and 17 beta-oestradiol in the aquatic environment

Adsorption of hydrophobic contaminants at the particle/water interface is one of the key processes controlling their fate in the aquatic environment. The sorption of the natural female hormones oestrone and 17-oestradiol has been studied under simulated riverine conditions. Both the kinetics and the effects of varying fundamental environmental parameters (e.g. sediment properties) on the thermodynamic equilibrium partition coefficient (K _p) have been studied in continuous and batch sorption experiments, respectively. Results showed that the sorption of oestrone and 17-oestradiol by sediment was relatively slow, reaching equilibrium in 50 days. In addition, relatively small adsorption of both oestrone and 17-oestradiol onto the sediment was observed, with K _p values between 200 and 250 mL g^–1. The comparable K _p values of the two compounds reflect their structural similarity. It can be concluded that the two endocrine disruptors, oestrone and 17-oestradiol remain primarily in association with the aqueous phase.     

Lead uptake from sea water and food,and lead loss in the common mussel Mytilus edulis

Common mussels, Mytilus edulis (shell length 19 to 21 mm, average dry weight 30 mg) were maintained for 6 weeks in sea water containing different concentrations of lead (0.005 to 5 mg · l^-1). The lead concentration in the mussels' whole soft parts was analysed at different times during the experiment. A constant rate of lead uptake, linearly dependent on the lead concentration of the medium, was observed. Thus, the temporal change of the concentration factor is also linear (regression coefficient 149.9 daily). Rate of lead loss, measured after transferring the mussels into natural sea water, is linearly dependent on the original lead concentration in the soft parts. Rates of uptake and loss in large mussels (shell length 45 to 55 mm, average dry weight 750 mg) are less than those in small mussels (shell length 19 to 21 mm, average dry weight 30 mg). During a much more extended experimental period, adjustment to a steady state is expected to occur; rates of lead uptake and loss are then non-linear. Lead uptake by individual organs (kidney, gills, adductor muscle, digestive gland, foot, mantle with gonads) of large M. edulis (shell length 45 to 55 mm, average dry weight 750 mg) was analysed in 2 test series. In the test series medium, the mussels were kept in a seawater medium containing 0.01 mg. Pb.l^-1. In the test series food, the mussels were kept in natural sea water but fed with the green algae Dunaliella marina containing lead (approximately 600 g.g^-1 dry weight). The lead quantity given per mussel per day was about 2 g in both test series. Within 35 days, the mussels of test series medium took up 29% of the total amount of lead given, those of test series food took up 23.5%. In all organs, lead concentration increased, but rates of uptake differed; the kidney displayed by far the highest rate of uptake. With these physiological properties M. edulis is an ideal indicator organism for lead pollution in the marine environment. A biologic calibration curve, the relationship between lead concentration in the mussels' whole soft parts at equilibrium and lead concentration in sea water, is presented.This paper forms part of a doctoral thesis in biology at Hamburg University     

Triterpenoid and caffeic acid derivatives in the leaves of ragweed, <Emphasis Type="Italic">Ambrosia artemisiifolia</Emphasis> L. (Asterales: Asteraceae), as feeding stimulants of <Emphasis Type="Italic">Ophraella communa</Emphasis> LeSage (Coleoptera: Chrysomelidae)

Summary. The leaf beetle Ophraella communa infests almost exclusively Ambrosia artemisiifolia in the fields of Japan, even though it normally feeds on several Asteraceous plants. A filter paper bioassay showed that the feeding of O. communa is strongly stimulated by methanolic extracts of A. artemisiifolia. The feeding stimulants for O. communa have been isolated from methanolic extracts of A. artemisiifolia. -Amyrin acetate, -amyrin acetate, 5-caffeoylquinic acid (chlorogenic acid) and 3,5-dicaffeoylquinic acid from A. artemisiifolia have been identified as feeding stimulants for O. communa. Triterpenoid derivatives (-amyrin acetate or -amyrin acetate) and caffeic acid derivatives (3, 5-dicaffoylquinic acid or 5-caffeoylquinic acid) showed feeding stimulant activity when mixed together.     

Stable isotope and biochemical fractionation in the marine pelagic food chain: the jellyfish Pelagia noctiluca and net zooplankton

In our field study we analyzed the C and H isotopic and biochemical (C, N, P, protein, lipid, carbohydrate) composition of the jellyfish Pelagia noctiluca (collected from the Gulf of Trieste in 1985 to 1986) and its presumed diet-net zooplankton. The mean ¹³C (-18.8) and D (-58.4) ratios of P. noctiluca showed enrichment in heavy isotopes relative to net zooplankton (2 for carbon and 30 for hydrogen). Both the jellyfish and net zooplankton were characterized by a linear correlation between ¹³C and D. C. N, P, protein, lipid, and carbohydrate contents of P. noctiluca were low on a dry weight basis as compared to net zooplankton. Significantly lower C:N and C:P ratios were found in jellyfish indicating a greater loss of carbon relative to nitrogen and phosphorus along the passage to a higher trophic level. Isotopic and biochemical evidence indicate that, though collected in nearshore waters, P. noctiluca depended on autochthonous marine organic matter.     

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.     

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.