Gas phase equilibria for dibenzo‐p‐dioxin,dibenzo‐p‐furan and biphenyl in the C‐H‐O system

The gas phase equilibrium calculation for the C‐H‐O system at atmospheric pressure and temperature from 773 to 1773 K at intervals of 250 K was performed to understand the generation and decomposition behavior of dibenzo‐p‐dioxin (DD), dibenzo‐p‐furan (DF) and biphenyl (BP) in relation to the existing oxygen potential. It is possible to categorize these results into three regions from the viewpoint of this potential: region (A), region (B) and region (C) are that of the higher, modest and lower oxygen potential, respectively. In region (A), the equilibrium amounts of DD, DF and BP are nearly zero. In region (B), they increase once and then decrease with rise in temperature. In the most characteristic region (C), they increase uniformly with rise in temperature.     

Effects of the Ellagic acid on the N‐Acetyltransferase activity and Acetylation of 2‐aminofluorene in the rat

The effects of the ellagic acid on the in vitro and in vivo acetylation of 2‐aminofluorene were investigated in male Sprague‐Dawley rats. For in vitro examination, cytosols with or without ellagic acid co‐treatment showed different percentage of 2‐aminofluorene acetylation. For in vivo examination, pre‐treatment of male rats with ellagic acid (10 mg/kg) 24h prior to the administration of 2‐aminofluorene (50 mg/kg) resulted in a 26% and 29%, respectively, decrease in the urinary and fecal recovery of N‐acetyl‐2‐aminofluorene, and a 37% decrease in the metabolic clearance of 2‐aminofluorene to N‐acetyl‐2‐aminofluorene. This is the first demonstration that ellagic acid decrease the N‐acetylation of carcinogens in vitro and in vivo.     

Synthesis and antithyroid activity of 6‐n‐propyl‐5‐arylazo‐2‐thiouracils †

The synthesis of several 6‐n‐propyl‐5‐arylazo‐2‐thiouracil derivatives was achieved. The antithyroid activity of these derivatives has been determined using iodine‐125‐thiocyanate discharge technique in rats, and 6‐n‐propyl‐2‐thiouracil (PTU) as a standard. None of the 5‐arylazo‐2‐thiouracil analogs showed antithyroid activity as compared to PTU. The structure‐activity relationships (SAR) of position 5 in the PTU molecule and the requirements for better binding to the proposed receptor are discussed.     

Photodecomposition of Isofenphos (O‐ethyl‐O(2‐isopropoxycarbonyl)‐phenyl)‐Isopropylphos‐Phoramidothioate)

Photodecomposition of the organophosphorus insecticide isofenphos (O‐ethyl‐O‐(2‐isopropoxy‐carbonyl)‐phenyl)‐N‐isopropylphosphoremidothioate) has been studied in solution, on glass and soil surfaces. Isofenphos underwent oxidation from P = S to the P = O group and deesterification on irradiation in hexane and methanol. Photoproducts were isolated and identified by spectroscopic methods.     

Alkylation of metals and the activity of metal‐alkyls†

The biochemical basis for resistance to metal ion toxicity is emerging though it is complicated by the different resistance mechanisms. Several strategies for resistance to toxic metal ions have been identified:

1. The development of energy driven efflux pumps which keep toxic element levels low in the interior of the cell. Such mechanisms have been described for Cd(II) and As(V).

2. Oxidation (e.g. AsO^2‐ to AsO₄ ^3‐) or reduction (e.g. Hg²⁺ to Hg⁰) can enzymatically and intracellularly convert a more toxic form of an element to a less toxic form.

3. The biosynthesis of intracellular polymers which serve as traps for the removal of metal ions from solution such as traps have been described for cadmium, calcium, nickel and copper.

4. The binding of metal ions to cell surfaces.

5. The precipitation of insoluble metal complexes (e.g. metal sulfides and metal oxides) at cell surfaces.

6. Biomethylation and transport through cell‐membranes by diffusion controlled processes.

In this short review I shall discuss the implications of biomethylation as a detoxification mechanism for microorganisms as well as for certain higher organisms.     

Transport of butyltins at the water‐air interface and the adsorptive behavior of tributyltin in the surface microlayer

The transfer dynamics and enrichment phenomena of monobutyltin chloride(MBT), dibutyltin chloride(DBT) and tributyltin chloride(TBT) at the water‐surface microlayer (SM) interface were studied. The transport processes of the three compounds at the interface are very fast in the estuarine environment. The mass transfer coefficients are 1.54 m/h for MBT, 2.16 m/h for DBT, 1.56 m/h for TBT. The effect of various factors, including pH, salinity, suspended particulate and temperature, on the adsorptive behavior of TBT in the water's surface microlayer was also studied.     

New O,O‐dimethyl (2,2,2‐trichloro‐1‐carbamoyloxy)‐ethyl phosphonates and their biological activity

A series of fifteen carbamoyl derivatives of O,O‐dimethyl (2,2,2‐trichloro‐l‐hydroxy) ethyl phosphonate (trichlorphon) was synthesized. A number of them showed higher insecticidal activity, having at the same time lower toxicity than the starting biologically active structure. A waste‐free technology for the production of the more promising representatives of this series could possibly be developed in the future.     

Pollution from polychlorodibenzo‐p‐dioxins and furans: The case of several foundry plants in the Lombardy region

In 1991 a co‐operation between Public Health Office (U.S.S.L.) n° 18 of Brescia and the Chemical Section Laboratories of U.S.S.L. n° 38 of Milan concerning the possible environmental impact of foundry industrial activities performing metallic scraps recovering, has been undertaken.

Soil and surfaces have been classified in conformity with the National Toxicological Consultative Commission (C.C.T.N.) recommendation dated 12/02/1988'; owing to the characteristics of the processed material, besides heavy metals, polychlorodibenzo‐p‐dioxins (PCDDs), polychlorodibenzofurans (PCDFs) and polychlorobiphenyls (PCBs) have been looked for.

The particulate matter collected from the filters positioned over the arc furnaces in 14 foundry plants has been characterized and classified, according both to C.C.T.N.¹ and to the Interministerial Board regulation dated 27/07/1985 for the first application of the Republic President Decree Law (D.P.R.) n° 915/1982, concerning wastes classification, based, in this case, on these toxic chlorinated compounds concentrations. From the very beginning, high levels of PCDDs and PCDFs have been detected, corroborating the very few literature data from foundry plants². The results obtained on 14 different foundries allow us to draw already some information, acceptable from the point of view of the statistical validity, about the pollution produced by this industry.     

The use of the embryo‐culture techniques in the research on the Teratogenic and Mutagenic properties of metals†

Actually, embryos can be cultured from the one‐cell stage up to the blastocyst stage, and their development can be easily monitored at any time: severe effects caused by toxic compounds are traduced by rapid embryonic death, less pronounced effects can be expressed by a lowered cleavage activity or by an arrest of the development from a particular stage. The system can be improved by transferring the embryos at the blastocyst stage in another more complete medium where they can “implant”; and form an inner cell mass with differentiated ectoderm and endoderm. Since last years, it has also become possible to culture postimplantation rodent embryos for short periods involving a number of particularly critical stages of organogenesis, such as the formation and closure of the anterior neuropore. Embryo‐culture also represents a useful system to study cytogenetic effects of chemicals which are often linked to lethal or teratogenic effects. These different possibilities are illustrated by examples of studies already performed with metals, and dealing with their teratogenic and/or cytogenetic effects on pre‐ and postimplantation rodents.     

Concentrations of polychlorinated dibenzo‐p‐dioxins and dibenzofurans in outdoor air of North‐Rhine‐Westphalia,Germany

Measurements of polychlorinated dibenzo‐p‐dioxins (PCDD) and dibenzofurans (PCDF) in outdoor air of North‐Rhine‐Westphalia were carried out. Fifty‐six samples were taken at different sites in areas of different land use and emission structures. A special filter system allowed analysis of the gas and particle phases separately. It was found that higher chlorinated PCDD/PCDF (7 or 8 chlorine atoms) are collected on glass fiber filter and lower chlorinated PCDD/PCDF (tetra‐ and penta‐CDD/CDF) are absorbed on polyurethane foam. The following isomers were determined: OCDD, OCDF and 11 isomers with chlorine substitution in 2,3,7,8‐position as well as the sum of TCDD, PeCDD, HxCDD, HpCDD, TCDF, PeCDF, HxCDF, HpCDF and the sum of PCDD (4–8) and PCDF (4–8). No 2,3,7,8‐TCDD could be detected but 2,3,7,8‐TCDF was found at 15 sites. Mean concentration in the Rhine‐Ruhr‐District for the sum of PCDD (4–8) and PCDF (4–8) was 3.2pg/m³ and 5.5pg/m³ respectively. Detection limit for TCDD and PCDD/PCDF (5–8) was 0.1–0.2 pg/m³ and 0.005–0.015 pg/m³ respectively. There is no significant indication that 2,3,7,8‐chlorinated isomers of PCDD/PCDF are predominantly decomposed by photochemical reactions in outdoor air.     

Planning for the monitoring of pollutants from non‐stationary combustion sources†

The most important constituents of traffic exhaust are carbon monoxide, nitrogen oxides, volatile organic compounds, polycyclic hydrocarbons and lead. Satisfactory analytical methods are available for measuring these compounds, but the required expenditure in their application to air pollution studies is quite different. Due to correlations between the concentrations of several exhaust components in road air conclusions regarding the expected level of some substances can be drawn by measurement of another emitted compound. But the selection of indicator compounds must be made under the aspect of the source‐specific relationship of emitted substances. The temporal and spatial distribution of air pollutants in street air is affected by traffic emissions more than by meteorological conditions. “Fingerprints”; of typical organic gaseous components of traffic exhaust also were found in residential areas.     

Photolytic decomposition of uc‐54229, a Proinsecticide of the Carbamate group

Phototransformation of UC‐54229 (1) [2,3‐dihydro‐2,2‐dimethyl‐7‐benzofuranyl‐N‐(trimethylamino acetyl)‐N‐methyl carbamate chloride] was studied under UV and visible light conditions. Photoirradiation of 1 with UV‐light resulted in the formation of five degradation products which on the basis of their mass and ¹H Nmr spectral analysis were characterised as 2, 3, 4, 5 and 6. It was observed that under the influence of light, UC‐54229 was degraded to acetyl‐carbofuran which under similar conditions underwent further transformation to the actual toxicant carbofuran. The degradation products or impurities present in 100% water soluble powder formulation were identified as carbofuran phenol and triethylamine hydrochloride.     

Mass spectral studies of 6‐n‐propyl‐2‐thiouracil,its oxygen,selenium and fluorinated congeners∗

The electron ionization mass spectra of the clinically used antithyroid agent 6‐n‐propyl‐2‐thiouracil (la), its minor metabolite, 6‐n‐propyluracil (lb) and their synthetic selenium and fluorinated analogs (1c and d) have been examined. The fragmentation pattern of these thiouracil and selenouracil studied bear strong similarities with those previously derived from a study of uracil analogs. Thus, the first step in the fragmentation is a retro Diel‐Alder decomposition with the loss of HCNX (X=O, S or Se) and the production of an ion radical which undergoes further fragmentation pathways which are discussed. 6‐n‐Propyl‐2‐selenouracil (1c) did show more complicated spectra due to the six natural isotopic abundance exhibited by the selenium atom. While the fluorinated analogs (1d) did substantiate the fact that the fragmentation pattern of these derivatives proceed through fragmentation between C₂ and N₃ bond since this produces the more resonance stabilized ion.     

Toxicity of 3‐Amino‐1: 2: 4‐Triazole to Activated Sludge Biomass

3‐amino‐1: 2: 4‐triazole (AT), a potent weed killer, added to activated sludge, caused immediate and drastic reduction in oxygen uptake by biomass. AT, a known specific inhibitor of catalases of animal and plant sources, did not appreciably alter catalase of activated sludge biomass.     

Cadmium in the terrestrial environment: Impact of long‐range atmospheric transport∗

Cadmium is supplied to Southern Norway in considerable amounts by atmospheric transport from other areas of Europe. This has caused a very marked increase of Cd levels in the natural environment in this area. Evidence of the main source areas is inferred from air concentration studies coupled to trajectory analysis. The extent of contamination is indicated from deposition studies and investigations of Cd in peat cores and surface soils, including soil profile distributions. The Cd content of vascular plants is substantially higher in Southern Norway than in areas farther north and further transfer in terrestrial food chains is occurring and may eventually lead to increased human exposure.     

Synthesis of 2,5‐diaryl‐2,4‐pentadienenitriles and their spectral,fluorescence and mutagenic properties

The condensation of substituted cinnamaldehydes and arylacetonitriles using sodium ethoxide in ethanol at room temperature afforded 2,5‐diaryl‐2,4‐pentadienenitriles in good yield. The structure of the reaction products was established on the basis of their infrared, nuclear magnetic resonance and elemental analysis data. Two representative compounds were studied for their mutagenic activity. One of them showed a weak mutagenicity while the second showed a high mutagenic activity in TA97a Salmonella strain. Both were negative in TA100. Some of these pentadienenitriles showed fluorescence in solutions.     

Cross‐sectional epidemiological study on the lead burden of children and workers in Greece

Exposure of the general population to lead in the environment is mainly caused by motor traffic exhaust and by industrial pollution. The aim of the study in Greece was to assess lead exposure in children living in point source impacted areas (Lavrion and Aspropyrgos‐Eleusis) using the biological monitoring parameter “blood lead concentration”;.

In addition, workers of a lead smelter, a battery plant and an oil refinery were investigated in these areas at the same time.

Five hundred and thirty‐four children and 105 workers took part in this investigation.

The highest blood lead levels (mean: 24.16 μg/100ml; range: 10.40–60.49 μg/100 ml) were found in children living in a 500m‐area around the lead smelter at Lavrion. Blood lead decreases corresponded to the increasing distance from the emitter. Nevertheless the values of children living in a 1500 m distance to the smelter are significantly higher than those of children living next to other kinds of industrial lead sources.

The mean values of the children living in the two industrial towns were manifold higher than those of the control group.

The blood lead levels of the investigated workers did not exceed the German BAT‐value (Biologischer Arbeitsstoff‐Toleranzwert) of 70 μg/100ml.     

Controlling pollution from land‐based sources in the Turkish Mediterranean coast—legislative aspects

The Turkish Mediterranean Coast is still the cleanest section in the region. This aspect needs to be strictly controlled and improved to allow for a sound development of touristic activities. Also, the adopted controlling policy should comply with the basic principles of the Mediterranean Action Plan. In Turkey, the regulations issued in connection with the “Water Products Law”; are now implemented to control wastewater discharges. Recently, major efforts were devoted to improve these regulations within the umbrella of the new “Environmental Law”;. The new proposals consider the issue from a much broader framework and provide technical support and criteria for marine outfalls, direct discharges of domestic and industrial sources and pretreatment requirement prior to discharge to the sewerage systems.     

Mechanistic aspects of the thermal formation of halogenated organic compounds including polychlorinated dibenzo‐p‐dioxins. Part V†: Hypotheses and summary

The hypotheses on the de novo syntheses of polychlorinated dibenzofurans (PCDFs) and polychlorinated dibenzo‐p‐dioxins (PCDDs), based on known literature, are presented. Polychlorinated benzenes and polychlorinated phenols are probably key intermediates.

In the present article, hypotheses that may account for the presence of polychlorinated dibenzofurans (PCDFs) and dibenzo‐p‐dioxins (PCDDs) in the effluents from municipal and industrial incinerators are put forward. These hypotheses are based on the previously surveyed literature (Ref. 203–206) and experimental results on laboratory scale and thermodynamic calculations are considered. The interconnections of various reaction steps are speculative and no technological information was added to account for conditions in real incinerators. Conclusion of the discussions on the related subject matter, presented in the Parts I‐IV (Ref. 203–206), are also described in this paper.     

Presence of Cd‐binding proteins in pre‐exposed and not pre‐exposed cadmium brine shrimp Artemia

The presence of metal binding proteins has been variously suggested as indicating involvement in uptake, storage, transport and elimination of toxic metals and in the routine metabolism of metals in mammals and a variety of marine invertebrates. This report describes results on the characterization of Cd‐BPs obtained from cadmium pre‐exposed and not pre‐exposed Anemia. The effect of pre‐exposure in the Cd‐binding protein induction in Artemia is discussed.