Polybrominated diphenyl ethers detected in human adipose tissue from Spain

Polybrominated diphenyl ethers (PBDEs) were detected in 13 human adipose tissue samples from Spain, 3 women and 10 men. Tetra-, penta- and hexabrominated diphenyl ethers were determined at ng/g lipid (ppb) level in all the samples. The average TeBDE level was 1.36 ng/g, the average PeBDE was 0.93 ng/g and the HxBDE 1.83 ng/g. Human adipose tissue levels of PBDE obtained in the current samples from Spain are comparable with the tissue levels reported in recent Swedish investigations.     

A model to assess the rate of evaporation of chemical compounds from surface waters

A model has been developed to assess the rate of evaporation of chemical compounds from surface waters. It is based on the two-boundary-layer model of Lewis and Whitman, on critically evaluated literature data and on specific experiments. The rate of evaporation is assessed as a function of the diffusion coefficient in air and water and of Henry's coefficient in water, being the physico-chemical parameters, and as a function of the wind speed, the water temperature and the water depth, being the environmental parameters.     

The formation of singlet oxygen in surface waters

The photochemical formation of singlet oxygen in some Dutch surface waters has been investigated using the method developed by Zepp (1). However, when monitoring the consumption of oxygen beside that of 2,5-dimethylfuran (DMF), the compound added to chemically snare singlet oxygen, it was found that appreciable, but varying parts of DMF were used up by secondary reactions leading largely to the same products, viz. cis- and trans-diacetylethylene. When taking the oxygen consumption as a measure for the singlet oxygen production on the basis of the stoichiometry of the primary reaction, a fair correlation between the singlet oxygen production and the total organic carbon (TOC) content was found for this selection of Dutch surface water samples. The steady-state concentrations of singlet oxygen determined in this way were about one order of magnitude lower than those found by Zepp (1) and by Zafiriou (2).     

Evaluation of biochemical effects related to perfluorooctane sulfonic acid exposure in organohalogen-contaminated great tit (Parus major) and blue tit (Parus caeruleus) nestlings

A perfluorooctane sulfonic acid (PFOS) biomonitoring survey was conducted on great tit (Parus major) and blue tit (Parus caeruleus) nestlings from Blokkersdijk, a bird reserve in the proximity of a fluorochemical plant in Antwerp (Belgium) and Fort IV, a control area. PFOS, together with 11 organochlorine pesticides, 20 polychlorinated biphenyl congeners and 7 polybrominated diphenyl ethers were measured in liver tissue. The hepatic PFOS concentrations at Blokkersdijk (86–2788 and 317–3322 ng/g wet weight (ww) for great and blue tit, respectively) were among the highest ever measured and were significantly higher than at the control area (17–206 and 69–514 ng/g ww for great and blue tit, respectively). The hepatic PFOS concentration was species- and sex-independent and correlated significantly and positively with the serum alanine aminotransferase activity and negatively with the serum cholesterol and triglyceride levels in both species but did not correlate with condition or serum protein concentration. In the great tit, a significant positive correlation was observed between the liver PFOS concentration and the relative liver weight. In the blue tit, the hepatic PFOS concentration correlated positively and significantly with hematocrite values. None of the investigated organohalogen pollutants except for PFOS were suggested to be involved in the observed biological alterations.     

Calibration of lichen transplants considering faint memory effects

Biomonitoring, among other purposes, can be used as a tool to study the dispersion of trace elements through the atmosphere and back to the earth's surface again. In this sense it has been used for more than 20 years now. Yet, the calibration of biomonitors elemental contents against other atmospheric element dispersion variables like deposition or airborne concentration is still an open subject. The knowledge of a calibration nevertheless represents a qualitative improvement upon the use of biomonitors. Biomonitors elemental contents are usually assumed to depend in a linear way on the average values of atmospheric element dispersion variables, thus a linear regression is assumed to provide a good calibration. In this work: the element dispersion variables like deposition or airborne concentration will be referred in general as availability variables due to reasons that will be clarified; an uptake experiment using transplants of lichen Parmelia sulcata carried out in Portugal during a 2-year period (1994/1996) is described; and new concepts and calibration methods are presented. Lichen and aerosol samples were analysed by nuclear analytical techniques PIXE and INAA, and total deposition dry residue samples were analysed by ICP-MS. A database of roughly 70,000 values was thus created and biomonitor calibration carried out considering that biomonitors are not mechanical instruments but that they rather describe their exposure with a non-perfect memory. Data shows that surveying lichens four times within 1 year, with a period of 3 months in between sampling campaigns, allows the recovery of availability mean, maxima and standard deviation for many elements.     

Analysis of volatile organic compounds, using the purge and trap injector coupled to a gas chromatograph/ion-trap mass spectrometer: review of the results in Dutch surface water of the Rhine, Meuse, Northern Delta Area and Westerscheldt, over the period 1992-1997

Volatile organic compounds are widely introduced into the Dutch aquatic environment. Liquid-liquid extraction and isolation by means of resins give poor recoveries for volatiles. In this study, a method has been developed to analyse these compounds with a purge and trap injection (PTI) coupled to a chromatograph/ion trap mass spectrometer. Volatile compounds are "purged" from the sample by carrier gas flow and transported through a condenser to a cooled trap. The bulk of liquid matrix is condensed in the condenser, while volatile compounds are left unaffected. The compounds of interest are trapped at a low temperature, by liquid nitrogen in the cooled trap of fused silica. Injection takes place by flash heating of the trap. The detection limits of the volatile compounds are in the range of 0.001-0.04 microgram l-1, in full spectrum mode. In this paper a review of the results in Dutch surface water of the Rhine, Meuse, Northern Delta Area and Westerscheldt, over the period 1992-1997, is presented. For calamities causing high levels of volatiles, the method is very useful. The compounds can be monitored over a certain period. In the Meuse, high levels of volatile organic compounds are observed. Diisopropyl ether at a maximum of 592 micrograms l-1.     

Fatty acids of the female horseshoe crab Xiphosura (Limulus) polyphemus

The fatty acid composition of 9 different tissues and organs of the female horseshoe crab Xiphosura (Limulus) polyphemus — one of the very few recent representatives of the ancient arthropod class Merostomata — was investigated in reference to the distribution of fatty acids through the marine food web. Fatty acid spectra, in which polyunsaturated fatty acids are predominant, especially eicosapentaenoic acid (20:5 3), revealed features characteristic of marine lipids. However, rather large quantities of monoenoic fatty acids also occur in all organs. In the saturated fatty acid fractions, the high content of branched-chain components is worth noticing, particularly in the gills and the carapace (35%); in all probability, the high amount of the branched-chain fatty acids is associated with their protective function in surface lipids. Isoprenoid fatty acids such as pristanic and phytanic acid were absent.     

Water-soluble components of four fuel oils: Chemical characterization and effects on growth of microalgae

Approximately 50% of the compounds in the water solubles from 4 fuel oils have been identified via gas chromatography and mass spectrometry. In addition to the well-described types of compounds (naphthalenes, benzenes) expected in water-soluble extracts we have found phenols, anilines, and indoles. Of these classes of compounds methyl, dimethyl, and trimethyl derivatives are present in relatively high concentrations. The water solubles from the 4 fuel oils showed considerably different inhibitory effects to growth of 6 microalgae, 2 blue-greens, 2 greens, and 2 diatoms. Two of the fuel-oil extracts, Baytown and Montana, were lethal to blue-green algae. This was in part traceable to their content of p-toluidine which was found to be toxic to Agmenellum quadruplicatum, Strain PR-6, 1 g in the algal lawn-pad assay and 100 g/l in liquid culture. The water-soluble fraction from New Jersey fuel oil was lethal to the 2 green algae, with lesser effects on the 2 blue-greens. The 2 estuarine diatoms used as test organisms were not greatly inhibited by Baytown, Montana, or New Jersey fuel-oil water-soluble extracts. However, earlier work with an American Petroleum Institute fuel oil and the diatom Thallassiosira pseudonana (3H) showed that 3H was a very sensitive organism. Water solubles from the Baton Rouge fuel oil were almost without effect on the growth of all 6 microalgae. On the basis of the work herein and earlier work, a very cautious viewpoint is advisable in generalizing on the toxicity or lack thereof of a given fuel oil on the growth of different kinds of microalgae. On the other hand, with water solubles from toxic fuel oils such as Baytown or New Jersey the data clearly suggest that their potential for environmental damage is high, either through selective or enrichment effects on natural populations or through a lowering of total primary production.     

Hochwasser 2002

In August 2002, highly contaminated areas in the region of Bitterfeld, e.g. the floodplain of the creek Spittelwasser, as well as the adjacent regions of Jeßnitz and Raguhn, were submerged by the river Mulde. An input of mobilized contaminated sediments in residential areas was the matter of concern. The objective of the present study was to estimate the pollutants load on the basis of chemical and biological data and identify the sources of pollutants. Deposited sludge and flood water samples were assessed on the basis of biological and chemical analyses and in comparison with administrative reference values. The pollution of the investigated sites was rather heterogeneous. At several sites, tolerance limits of the German Klärschlammverordnung or the Bundesbodenschutzverordnung were clearly exceeded, e.g. for Pb, As and HCH. Organic extracts exhibited significant effects in several biotests. This may be relevant with respect to direct particle uptake via ingestion or respiration. Pollution patterns for heavy metals as well as for organic pollutants differed significantly from the pattern found in the Spittelwasser flood plain before the inundation, which is in contrast to the initial hypothesis of a possible transport of contaminated Spittelwasser sediments into residential areas. Interestingly, a correlation of chemical load and the overall biological effect could be shown. From the viewpoint of the precautionary principle, the identification of the compounds exerting toxic effects and of the respective pollutant sources would be desirable.