Degradation of Poly(Ethylene Glycol)-Based Nonionic Surfactants by Different Bacterial Isolates from River Water

Different bacterial strains able to attack polyoxyethylene-type nonionic surfactants were isolated by enrichment procedure from the surface waters of the Arno River. Alkylphenol polyethoxylates and alkyl polyethoxylates, as well as polyethylene glycols, were degraded and assimilated by bacterial strains in axenic cultures. Degradative routes of polyethyleneoxide chains were investigated by matching each bacterial isolate with several types of nonionic surfactants and polyethers and by the identification of their degradation products isolated during aerobic digestion experiments. In accordance with previous reports, the first attack led to the shortening of the poly(oxyethylene) chains of the nonionic surfactants. It was found that the strains able to degrade PEG segments of nonionic surfactants possess enzymatic systems unable to degrade free PEGs, whereas those degrading the latter substrates cannot degrade PEG segments coupled to hydrophobic moieties.     

Geochemical caper fingerprints as a tool for geographical origin identification

The identification of geographical origin of food products is important for both consumers and producers to ensure quality and avoid label falsifications. The caper plant (Capparis spinosa L., Brassicales Capparidaceae), a xerophytic shrub common in the Mediterranean area, produces buds and fruits that are commercialized in brine at high price. Those grown in Italy in the Aeolian Islands are renowned for their high quality. This study is aimed to establish a correlation between the geological and geochemical features of soil and the chemical composition of caper buds grown in two Aeolian Islands, Lipari and Salina. Major and trace elements were investigated by X-ray fluorescence and inductively coupled plasma-mass spectrometry in soil and caper samples from three localities in Lipari and Salina, and data from the three sites were compared by a nonparametric test, a correlation test and multivariate statistics (principal component analysis). The results allowed to discriminate soils according to geolithological characteristics of each area and detect a statistically significant correspondence between soil and caper samples for the elements Co, Fe, Mg and Rb, identifying thus possible geochemical caper fingerprints of origin. These results may also be useful to protect the high quality of Aeolian caper products by a suitable “Made in Italy” trademark and avoid falsifications and frauds.     

Phytotoxicity to and uptake of enrofloxacin in crop plants

Phytotoxicity of enrofloxacin on crop plants Cucumis sativus, Lactuca sativa, Phaseolus vulgaris and Raphanus sativus was determined in a laboratory model: the effect of 50, 100 and 5000 microgl(-1) were evaluated after 30 days exposure by measuring post-germinative growth of primary root, hypocotyl, cotyledons and leaves. Concentrations between 50 and 5000 microgl(-1) induced both toxic effect and hormesis in plants, by significantly modifying both length of primary root, hypocotyl, cotyledons and the number/length of leaves. A toxic effect is induced by high concentration (5000 microgl(-1)), while hormesis occurs at low concentrations (50 and 100 microgl(-1)). A continuum between toxic effect and hormesis is found in the four plant species. Both toxic effect and hormesis can be related to an efficient plant drug uptake, in the order of microgg(-1). Plants are able to metabolize enrofloxacin into ciprofloxacin, as also happens in animals; Cucumis, Lactuca and Phaseolus biologically convert about one quarter of stored enrofloxacin. The ecological implication of enrofloxacin contamination in terrestrial environments is discussed.     

OH-initiated oxidation of DMS/DMSO: reaction products at high NOx levels

Dimethylsulphide (DMS) gas phase oxidation with OH radicals was investigated by long path FT-IR spectroscopy and by ion chromatography (IC) and HPLC-MS2 to quantify the reaction products and evaluate heterogeneous processes. The experiments were performed considering two different NOx (NO2+NO) levels. The initial concentration of NO2 was varied from 24 ppbV (NOx=1 ppmV) to 953 ppbV (NOx=10 ppmV). Photolysis of H2O2 was used as the OH-radical source. SO2, dimethylsulphoxide (DMSO), dimethylsulphone (DMSO2), methanesulphonic acid (MSA), methanesulphinic acid (MSIA) and methane sulphonyl peroxynitrate (MSPN) were identified as the main sulphur-containing products. The results indicate that higher NOx levels play a significant role in the chemistry of CH3S(O)x radical, influencing both the SO2/MSPN ratio and the amount of the sulphur species in the condensed phase, and that the NO2/NO ratio could influence the trends in the molar yields of the different products. For this reason the NOx content results a limiting parameter when on measure DMS in atmospheric environment.     

Behavior of Chlorpyrifos-methyl in soil and sediment

This research was carried out with the aim of obtaining information regarding the possible environmental impact of Chlorpyrifos-methyl, an organophosphoric insecticide used in agriculture for its phytoiatric action against Hemiptera, Lepidoptera, Coleoptera, and Diptera. Studies relating to the degradation kinetics of the insecticide in two soils and one sediment have shown a rapid degradation process in all three. The prevalent form of degradation would appear to be the chemical type, because the degradation kinetics in a sterile soil have not demonstrated that micro-organisms play a significant part. The adsorption isotherms showed that the insecticide has a greater affinity for the sediment (Kf=143) as opposed to the soils (Kf=65) and that the adsorption process is practically irreversible. Moreover, hydrolysis tests in buffered solutions at pH 4, 7, and 9 revealed that the molecule is particularly unstable with a basic pH.