Effects of the level of dietary protein on the toxicity of hexachlorocyclohexane in rats

Male albino rats were fed for 28 days from weaning on diets containing 5% (group 1), 10% (group 2) and 21% (group 3, normal protein) protein as casein. At the end of dietary period, HCH was administered daily for 30 days to investigate the interaction between protein deficiency and pesticide toxicity. The results indicated that rats fed a lower protein diet and HCH had a higher mortality, lower rate of growth, increased liver weight and deposition of the pesticide in blood and tissues in larger amounts. Blood pressure (systolic and diastolic) was significantly increased and the heart rate showed tachycardia in low protein exposed animals. A significant increase of total lipids, cholesterol, triglycirides, free fatty acids in serum and tissues of animals exposed to low protein was observed. A close correlation existed between lipid accumulation and storage of HCH in tissues and dietary protein seemed to play an important role in detoxification.     

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.     

Electron microscopy documenting the cellular metabolic fate of Zn IONS∗

In vertebrates and invertebrates Zn exist as complexed compounds with metallothioneins. However, its cellular level effects and metabolic fates are scantly documented. In the elucidation of this fact, EM results on hepatic cellular alterations in fish under lethal dose exposure at 4.0 ppm over a week is illustrated.

A large number of lysosomes in hepatic cells prevailed on exposure to Zn in its sulfate form. Evidently, due to metal compound stress and cellular damage lysosomal activity is augmented. The lysosomes harboured digestible material, presumably the aforementioned substrates. Contrary to it, fat droplets prevailed while glycogen depletion is noticeable. Unlike the effects of Hg, the nuclei were normal with granular chromatin and prominent nucleoli. However, the mitochondria contained some small intramitochondrial bodies. Similar to the effects of Hg, the cell membrane remained intact.

In vivo enzymatic studies indicated augmentation in catalase, acid‐ and alkaline‐phosphatases, while glucose‐6‐phosphatase is inhibited. However, only alkaline‐ and glucose‐6‐phosphatases are inhibited under in vitro conditions.

Thus, it is evident that Zn enhances cellular bioenergetic requirements culminating in glycogen depletion owing to stress, concomitantly envisaging inhibition of oxidative phosphorylation in the electron transport system.     

Characterization of airborne particulate matter in thessaloniki,Greece

TSP samples, collected at two stations in the area of Thessaloniki during the period July 1987‐June 1988, were analysed for heavy metals (Fe, Pb, Zn, Cu, Mn, Cr, Co, Ni and V). Flame and flameless atomic absorption spectrophotometry was used for metal determinations. Metals determined were characterized with respect to their origin from natural or man‐made emission sources. Source identification was attempted by relation of metal concentrations to wind direction, and interelement correlations.

Results obtained showed that Pb, Zn and Cu are emitted from man‐made sources (traffic, domestic heating, industry), V, Ni and Co are derived partially from natural and man‐made sources, while Cr is mainly soil‐derived.     

Environmental degradation of atrazine,linuron and fenitrothion in soil samples

The persistence of atrazine, linuron and fenitrothion in soil samples from an estuarine area (Ebro delta, Tarragona, Spain) has been studied. Soil samples from the top surface (10 cm) were collected during 1989–91, freeze‐dried, sieved through 200 μm, Soxhlet extracted with methanol, cleaned‐up with Florisil and analysed either by gas chromatography‐nitrogen phosphorus detection (GC‐NPD), in the case of atrazine and fenitrothion, or by liquid chromatography with diode array detection (LC‐DAD), for linuron. Confirmation of the samples analysed by GC‐NPD was carried out using GC‐mass spectrometric detection (MS) in the electron impact mode. The soil half lives obtained under the real environmental conditions have been calculated and the values obtained have been correlated with the physicochemical properties of each pesticide and the soil type. Degradation was affected by volatilization since temperatures in the area of study are relatively high, ca. 30°C, in the summer period. In the case of atrazine it has been shown that deethylatrazine is formed in all the samples studied..     

Photodegradation of the organophosphorus herbicide “anilophos”

Photodecomposition of the organophosphorus herbicide anilophos [S‐(N‐(4‐chlorophenyl) N‐isopropyl carbaniloyl methyl] 0,0‐dimethyl phosphorodithioate has been studied in methanol. It underwent oxidation, hydrolysis and dimerisation on irradiation with U.V. light and produced a number of photoproducts which were characterised by ¹H‐NMR and Mass spectroscopy.     

HO ‐ initiated oxidation of acridine and aminacrine in aqueous media: Kinetic model

The photodecomposition of diluted aqueous solutions of acridine and aminacrine in the presence of hydrogen peroxide was studied. Irradiation was carried out with a low pressure mercury vapour lamp. The kinetic model describes the photodegradation rate of the organic compound with respect to the technological parameters of the reactor and provides the reaction rate constants of hydroxyl radicals towards these two molecules. This model was extented to high hydrogen peroxide concentrations ([H₂O₂] > 200 μmol/l) by considering the reactivity of hydroxyl radicals towards hydrogen peroxide. This assumption allows us to define an optimal hydrogen peroxide concentration.     

Assessment of hydrocarbon emissions from diesel invert mud residues treated in a bioreactor

Hydrocarbon emissions from a diesel invert mud residue (DIMR) were monitored while the hydrocarbons were being biodegraded in a solid‐phase bioreactor. Five to twenty percent of the reduction in diesel hydrocarbons was attributed to evaporation depending on the treatment, i.e. homogenization, cultivation, and aeration. Most of these volatile hydrocarbons were linear C₈ — C₁₂ alkanes and one‐ring aromatics. Of the treatments aeration had the largest effect on emissions; forced air through the bottom of the bioreactor cells increased emissions by three times over that of the non‐aerated cells. Cultivation increased hydrocarbon emission concentration as much as twofold over the pre‐cultivation value, however, emissions returned to the original levels within 12 hours. Homogenization had the least effect of all treatments. Diurnally, the emission rate was 40% higher in late afternoon than at midnight; the cause of which was probably atmospheric fluctuations such as temperature and solar radiation. The effects of daily atmospheric fluctuations were empirically modeled and taken into account for determining the total volume of emissions.     

Compilation of EINECS: Descriptions and definitions used for substances,impurities and mixtures

The European INventory of Existing commercial Chemical Substances (EINECS) lists all substances which were on the European Community Market between 1 January 1971 and 18 September 1981. Substances on EINECS are known as ‘existing’ substances. The EINECS inventory was drawn up by the European Commission to meet the requirements of article 13 of Directive 79/831/EEC [1]. EINECS was published in the Official Journal of the European Communities in 1990 [2]. This paper describes how individual substances, impurities and mixtures were defined and dealt with when registered for the EINECS inventory. It is the first in a series of such papers.     

Potentiometric studies of mixed complexes of cobalt(II) and copper(II) with l‐Asparagine and adenine

A potentiometric titration technique has been used to determine the stability constants for the various complexes of Co(II) and Cu(II) with L‐asparagine and from DNA base, e.g. adenine. Stability constants of ternary systems have been evaluated by the method suggested by Irwing‐Rossotti. In addition, the conditional constants were calculated as a function of pH. The maximum values of the conditional formation constants were found to be in accordance with the mixed‐ligand complex formation constants in a determined pH region. Furthermore, the molar fractions of different species from mixed complexes were calculated by means of formation constants. The values of stability constants of mixed‐ligand complexes at 25°C are as follows: log K= 5.25 for Co(II)‐L‐asparagine‐adenine; log K= 9.30 for Cu(II)‐L‐asparagine‐adenine. The ionic strength was kept constant at I = 0.20 with NaClO₄.