Trees as bioindicator of heavy metal pollution in three European cities

Concentrations of four heavy metals were determined in tree leaves and bark collected from polluted and non-polluted areas of three European cities (Salzburg, Belgrade and Thessaloniki) for a comparative study. Platanus orientalis L. and Pinus nigra Arn., widespread in urban northern and southern Europe, were tested for their suitability for air quality biomonitoring. Leaves and barks were collected uniformly of an initial quantity of about 30 g of each sample. Analysis was accomplished by electrothermal atomic absorption spectrometry after total digestion. Site-dependent variations were found with the highest concentration level measured in Belgrade, followed by Thessaloniki and Salzburg. A higher accumulation of heavy metals was found in bark compared to leaves. Pine tree bark, accumulating higher concentrations of trace metals compared to plane tree bark, shows a higher efficiency as bioindicator for urban pollution. Both indicator species are suitable for comparative studies on bioindication of urban air pollution.     

Chemical fractionation of copper, lead and zinc in ombrotrophic peat

Measurement of operationally defined chemical fractions in ombrotrophic peat samples provides information not obtained by total metal extractions. Examination of such sequential data permits interpretation of process dynamics. Results for copper, lead and zinc chemical fractionation of peat profiles from Ringinglow Bog, near Sheffield, Great Britain, are reported and discussed. Lead and zinc share similar patterns of partitioning. A considerable proportion of these records is in a form predisposed to transformation and mobilisation. In contrast, much of the copper is comparatively immobile, it being associated with the more chemically intractable fractions. The results suggest that peat copper deposition records may be used for reconstruction of pollution history. The use of lead and zinc records for these purposes is problematic.     

Relation of length and sex to selenium concentrations in mosquitofish

Analysis of mosquitofish, Gambusia affinis, has proven useful for monitoring contaminant levels in aquatic biota; however, the small size of this species often requires the compositing of several fish to provide sufficient biomass for selenium analysis. Such composites have usually been obtained without considering the length and sex of the individual fish. The present study found significant differences in mean lengths and sex ratios of mosquitofish sampled with small-mesh dip nets from five sites close to each other in the San Joaquin Valley, California. To test the effect of these different sample characteristics, fish from each site were divided by sex into five size classes (<20, 20-30, 31-45, 46-60, and >60mm total length) before analysis for total selenium. Altogether, fish from the San Luis Drain and Kesterson Ponds 2 and 7 contained 65-360 microg g(-1) selenium (dry weight basis), or about 28- to 300-fold more than concentrations in fish of the same length and sex from the Volta Wasteway and Volta Pond 26. Except for females 31-45 mm long from the San Luis Drain that had higher concentrations than either smaller or larger females, selenium concentrations did not differ significantly among size classes. Although concentrations differed between sexes in samples from the San Luis Drain, Kesterson Pond 2, and Volta Pond 26, neither males nor females consistently had the higher concentrations. In the San Luis Drain, 20-30 and 31-45 mm long females had higher concentrations than did males of the same size classes; in Kesterson Pond 2 and Volta Pond 26, however, 20-30 mm long males had higher concentrations than did females of the same size class. Although no consistent patterns were observed, the occasional differences in selenium concentrations in fish of different length and sex indicate that these variables should be considered when surveys and monitoring studies are designed.     

The total carbohydrate: organic carbon ratio as an indicator of sewage-derived organic matter in Burbo Bight sediments, Liverpool Bay, UK

Sediments from the Burbo Bight, Liverpool Bay, were analysed for their total carbohydrate (TCH) and organic carbon (TOC) contents, and the TCH:TOC ratio (when the TCH is expressed as a percentage of the TOC) was used to give an indication of the amount of sewage-derived organic matter in the sediments. The %TCH values found ranged from 17-68 with an average of 40, indicating that sewage-derived organic matter constituted a significant fraction of the organic matter in the sediment. This appears likely to have been derived mainly from the Mersey Estuary outflow and the sewage sludge dumped in Liverpool Bay, but these two sources cannot be distinguished using this technique. It is suggested that further studies are required on the carbohydrates in sewage sludge and coastal sediments to satisfactorily establish this technique.     

Heavy metal concentrations in the liver of three duck species: influence of species and sex

To investigate interspecific and intersex differences in heavy metal levels, we analysed concentrations of cadmium, cobalt, chromium, copper, lead, mercury, manganese, nickel and zinc in the livers of male and female black duck (Anas rubripes), mallard (A. platyrhynchos) and greater scaup (Aythya marila) collected in Raritan Bay, New Jersey in December 1980 and January 1981. Certain metal levels varied significantly by species and sex. In all species, Zn and Cu had the highest concentrations, and Cd, Co, and Hg were lowest in all three species. Scaup had significantly higher levels of Cu than black ducks and mallards, and mallards had significantly higher levels of Mn and Zn than black duck and scaup. Overall, eight of nine metal levels were higher in male than female black duck. In scaup, females had significantly higher levels of Pb and Mn than males. In black ducks, males had significantly higher levels of Cu, Mn and Zn than females. The sample of mallard was too small to test intersex differences.     

The effect of pH on zinc adsorption equilibria and exchangeable zinc pools in soils

Zinc adsorption equilibria were measured in soils differing in pH but with similar textures and total zinc concentrations, using adsorption isotherm and isotopic exchange techniques. The results suggested that the equilibrium between solution and exchangeable zinc was strongly pH dependent and the active zinc species in adsorption was single charged (e.g. Zn(OH)(+)). The size of the exchangeable zinc pool was not strongly pH dependent. Similar results were obtained when zinc was added to the soils, either as Zn(NO(3))(2) or in sewage sludge.     

Boreal bog plants: nitrogen sources and uptake of recently deposited nitrogen

The main goals of this study were to determine the delta15N signature of quantitatively important boreal bog plants as basis for discussing their N sources, and to assess the effects of five different 3 year N treatments (i.e. 0, 5, 10, 20 and 40 kg N ha(-1) year(-1)) on the bog plants and surface peat at different depths (i.e. 0, 5, 10, 20 and 40 cm) by using 15N as tracer. Plants and peat were analyzed for N concentration, 15N natural abundance and 15N at.%. From the results we draw three main conclusions: First, the relative importance of different N sources is species-specific among bog plants. Second, an annual addition of 5 kg N ha(-1) year(-1) was sufficient to significantly increase the N concentration in Sphagnum mosses, liverworts and shallow rooted vascular plants, and an annual addition of 40 kg N ha(-1) year(-1) during 3 years was not sufficient to increase the N concentration in deep rooted plants, although the 15N content increased continuously, indicating a possible longer term effect. Third, an annual addition of 40 kg N ha(-1) year(-1) during 3 years increased the N content in surface peat at depths of 5 and 10 cm, but not at depths of 20 and 40 cm, indicating the capacity of the living Sphagnum mosses and the surface peat to take up deposited N, and thereby function as a filter.     

Dissolved organic matter fractions formed during composting of winery and distillery residues: evaluation of the process by fluorescence excitation-emission matrix

The aim of the present paper is to assess the maturity degree reached by different samples of several mixtures from winery and distillery residues composted using the Rutgers composting system, by means of excitation-emission matrix (EEM) fluorescence spectroscopy. The composts were sampled once a week for about 200d. EEM spectra indicate the presence of different fluorophores. The fluorescence intensities of these peaks show trends related to the maturity of the composting samples selected. The "contour density" of EEM maps is strongly modified through time. We have used the quantitative method of fluorescence regional integration (FRI). The EEMs were delineated into five excitation-emission regions. The degree of compost maturity could be correlated with the percentage of the volumetric integration under the EEM within each region. Further refinement of these techniques should provide a relatively rapid method for assessing the suitability of the compost to soil application.     

PAH and soot emissions from burning components of medical waste: examination/surgical gloves and cotton pads

This is a laboratory investigation on the emissions from batch combustion of representative infectious ("red bag") medical waste components, such as medical examination latex gloves and sterile cotton pads. Plastics and cloth account for the majority of the red bag wastes by mass and, certainly, by volume. An electrically heated, horizontal muffle furnace was used for batch combustion of small quantities of shredded fuels (0.5-1.5 g) at a gas temperature of approximately 1000 degrees C. The residence time of the post-combustion gases in the furnace was approximately 1 s. At the exit of the furnace, the following emissions were measured: CO, CO2, NOx, particulates and polynuclear aromatic compounds (PACs). The first three gaseous emissions were measured with continuous gas analyzers. Soot and PAC emissions were simultaneously measured by passing the furnace effluent through a filter (to collect condensed-phase PACs) and a bed of XAD-4 adsorbent (to capture gaseous-phase PACs). Analysis involved soxhlet extraction, followed by gas chromatography-mass spectrometry (GC-MS). Results were contrasted with previously measured emissions from batch combustion of pulverized coal and tire-derived fuel (TDF) under similar conditions. Results showed that the particulate soot) and cumulative PAC emissions from batch combustion of latex gloves were more than an order of magnitude higher than those from cotton pads. The following values are indicative of the relative trends (but not necessarily absolute values) in emission yields: 26% of the mass of the latex was converted to soot, 11% of which was condensed PAC. Only 2% of the mass of cotton pads was converted to soot, and only 3% of the weight of that soot was condensed PAC. The PAC yields from latex were comparable to those from TDF. The PAC yields from cotton were higher than those from coal. A notable exception to this trend was that the three-ring gas-phase PAC yields from cotton were more significant than those from latex. Emission yields of CO and CO2 from batch combustion of cotton were, respectively, comparable and higher than those from latex, despite the fact that the carbon content of cotton was half that of latex. This is indicative of the more effective combustion of cotton. Nearly all of the mass of carbon of cotton gasified to CO and CO2 while only small fractions of the carbon in latex were converted to CO2 and CO (20% and 10%, respectively). Yields of NOx from batch combustions of latex and cotton accounted for 15% and 12%, respectively, of the mass of fuel nitrogen indicating that more fuel nitrogen was converted to NOx in the former case, possibly due to higher flame temperatures. No SO2 emissions were detected, indicating that during the fuel-rich combustion of latex, its sulfur content was converted to other compounds (such as H2S) or remained in the soot.