Inhibition of plasma butyrylcholinesterase activity in the lizard Gallotia galloti palmae by pesticides: a field study

A field study was performed to evaluate the effect of exposure to organophosphorus (OP) and carbamate (CB) pesticides on the lizard Gallotia galloti palmae. Butyrylcholinesterase (BChE) activity was measured in the plasma of 420 lizards collected from agricultural and reference areas on the Island of La Palma (Canary Islands, Spain) in two sampling periods. Exposure to cholinesterase-inhibiting pesticides was evaluated by a statistical criterion based on a threshold value (two standard deviations below the mean enzyme activity) calculated for the reference group, and a chemical criterion based on the in vitro reactivation of BChE activity using pyridine-2-aldoxime methochloride (2-PAM) or after water dilution of the sample. Mean (+/- SD) BChE activity for lizards from agricultural areas was significantly lower (Fuencaliente site = 2.00 +/- 0.98 micromol min(-1) ml(-1), Tazacorte site = 2.88 +/- 1.08) than that for lizards from the reference areas (Los Llanos site = 3.06 +/- 1.17 micromol min(-1) ml(-1), Tigalate site = 3.96 +/- 1.62). According to the statistical criterion, the number of lizards with BChE depressed was higher at Fuencaliente (22% of males and 25.4% of females) than that sampled at Tazacorte (7.8% of males and 6.2% of females). According to the chemical criterion, Fuencaliente also yielded a higher number of individuals (112 males and 47 females) with BChE activity inhibited by both OP and CB pesticides. CBs appeared to be the pesticides most responsible for BChE inhibition because most of the samples showed reactivation of BChE activity after water treatment (63.3% from Fuencaliente and 29% from Tazacorte). We concluded that the use of reactivation techniques on plasma BChE activity is a better and more accurate method for assessing field exposure to OP/CB pesticides in this lizard species than making direct comparisons of enzyme activity levels between sampling areas.     

Effect of Long Retention Time in the Settler on Phosphorus Removal from Communal Wastewater (4 pp)

- Goals. The objective of the paper is to illustrate the solution of a chronic problem occurring in a wastewater treatment facility with a capacity of 12,000 inhabitant equivalent. A drastic phosphorus concentration increase (two or three times higher than the Hungarian limit of 1 mg/l) was observed in the wastewater treatment facility for a long time (12–24 h) with changing time periods indicating malfunctioning in the operation of the facility. Methods Computer-aided simulation technique was used to develop a solution for the treatment of the problem using a software developed by the Department of Environmental and Chemical Engineering, University of Veszprém, Hungary. Results and Discussion The simulation studies show that if the nightly inflow is less than 200 m3/h at least for two hours, the system doesn't then receive enough fresh nutrients which can cause a deficiency in the nutrient uptake of the PAOs in the anaerobic zones. This can result in the fact that the PAOs accumulate less phosphorus into the aerobic zones. Conclusion Long retention time (10 h) is the reason for the problem, namely – under special conditions – the phosphorus in the sludge of the settling tank of the wastewater treatment plant. The problem was caused by phosphorus dissolution from the sludge of the settling tank during the undesirably long retention time.     

Online hourly determination of 62 VOCs in ambient air: system evaluation and comparison with another two analytical techniques

This paper presents results of the processing and validation of data collected by an automatic gas chromatograph (AGC). This system was used to monitor 62 volatile organic compounds (VOCs) in urban air in the Basque Country, Spain. The nonpolar compounds (C2-C10) identified-paraffins, olefins, aromatics, and chlorinated compounds-accounted for 88% of the mass of total non-methane hydrocarbons (TNMHCs) in ambient air. The evaluation of linearity, precision, detection limits (DLs), and stability of retention times (RTs) indicates that the equipment is suitable for measuring ambient air automatically for prolonged periods (6 months). The calibration of the equipment using response factors calculated on the basis of the effective carbon number (ECN) showed variations of over 10% for acetylene, isoprene, and n-hexane. The results provided by the automatic chromatograph correlated significantly with simultaneous results from other widely used techniques for determining VOCs in ambient air: (1) portable GC, equipped with photoionization detector (PID), and (2) active adsorption on Tenax-TA followed by thermal desorption and chromatographic analysis.     

Relationship between two consecutive lactations and fat level in persistent organochlorine compound concentrations in human breast milk

An attempt was made to understand how consecutive deliveries and the following lactations have an impact on the organochlorine compound levels detected in human milk. The other goal of the study was to check for a possible dependence between fat content and the levels of the studied compounds in milk samples from the same lactations. 199 milk samples were examined for the presence of p,p'-DDT, p,p'-DDE, p,p'-DDD, alpha-, beta-, gamma-HCH and sigmaPCBs. Moreover, in 87 milk samples the fat content was additionally determined. This study has indicated that, for the mother with a shorter interval between lactations, mean concentrations of the examined compounds were higher in the milk of the first lactation than that of the second. For the other donor whose second lactation began after 2 years, the mean levels of HCB, beta-HCH, p,p'-DDD, and PCBs in her milk were higher during the first lactation. At the same time, the concentrations of p,p'-DDT and p,p'-DDE after the second delivery were slightly higher. The correlation coefficients between the two data sets (fat content in milk, concentrations of the compounds studied in milk) showed no interrelationship between them.     

Phytoavailability and extractability of potassium, magnesium and manganese in calcareous soil amended with olive oil wastewater

Land disposal of olive oil wastewater using it as a soil amendment requires a knowledge of the effects that its application may produce on the status of the mineral nutrients in the plant-soil system. A pot experiment using calcareous soil was performed in a growth chamber to examine the effects of olive oil wastewater on the availability and postharvest soil extractability of K, Mg and Mn. The experiment included 6 treatments: two rates of olive oil wastewater, two mineral fertilizer treatments containing K (which supplied K in amounts equivalent to the K supplied by the olive oil wastewater treatments), a K-free mineral fertilizer treatment, and a control. The pots were sown with ryegrass as the test plant, harvesting 3 times at intervals of one month. Olive oil wastewater has demonstrated a considerable capacity for supplying K that can be assimilated by the plant, tending in fact to surpass the mineral potassium fertilizer tested. The application of olive oil wastewater tends to reduce the concentration of Mg in the plant, similarly to the effect of adding mineral potassium fertilizer. An enhancement of Mn availability takes place in the soil amended with olive oil wastewater, which on occasion has produced Mn concentrations in plant that could be considered phytotoxic or at least excessive. After harvesting, we observed an increase in the amount of exchangeable K in soil with added industrial wastewater. However, these increases are lower than those in soil treated with mineral potassium fertilizer. The levels of exchangeable, carbonate-bound, organic-bound and residual Mg in soil were higher in treatments incorporating olive oil wastewater than in those with added mineral K, with the opposite tendency occurring in the amount of Fe-Mn oxides-bound Mg in soil. Treatments based on olive oil wastewater, especially in high doses, increased the amount of exchangeable and carbonate-bound Mn in soil, in comparison with treatments adding mineral fertilizers with or without K. In contrast, the addition of industrial wastewater caused a drop in the amount of Fe-Mn oxides-bound and organic-bound Mn in soil.     

Interaction of limestone grains and acidic solutions from the oxidation of pyrite tailings

To characterise the coatings formed and to analyse element partitioning between the aqueous and solid phase, suspensions were prepared with four grain sizes of limestone and three different amounts of acidic solution from oxidized pyrite tailings. In all cases, red coatings with three different layers covered the grain surface, sealing off the acidic solution. The inner layer was composed mainly of basaluminite, the middle layer of schwertmannite, and the outer layer of gypsum and jarosite. Zn, Cd and Tl were co-precipitated by Fe and Al; As and Pb were co-precipitated almost completely by Fe; and Cu formed mainly Cu sulphates. All trace elements reached almost total precipitation at pH 6.3, but the precipitation of As and Pb tended to decrease as the pH rose. Consequently, liming should be calculated so that the soil pH does not exceed 6.3. This calculation should take into account that the armouring of the limestone grains can cause underestimations in the amount of liming material needed.     

Allelopathic effects of aconitic acid on wild poinsettia (Euphorbia heterophylla) and morningglory (Ipomoea grandifolia)

High infestations of alexandergrass (Brachiaria plantaginea) in experimental area have reduced seedbank of some weed species in soil at a greater degree compared to those obtained with the use of an efficient herbicide. Aconitic acid (AA) has been identified in those plants in high concentration. Thus, two experiments were carried out in the laboratory to determine the effects of pure AA on weed seed germination and on endophytic fungi in wild poinsettia (Euphorbia heterophylla) and morningglory (Ipomoea grandifolia) weed species. Doses of AA (0, 0.5, 1.0, and 2.0 mM) were introduced in agar-water 0.5% medium and weed seeds treated with and without external sterilization by sodium hypochloride. Four replications of fifty seeds of each species by treatment were sown in plastic boxes with cover and maintained in germination chamber for 12 days. Reduction in germination rate, root and stem growth were observed in both species, as well as reduction in root number in morningglory were also observed at 2.0 mM concentration of AA. An increase in number of seeds with presence of endophytic fungi was also observed in both species, independently of seed sterilization, mainly of a green type fungi coloration in wild poinsettia. Aconitic acid presents allelopathic activity and can stimulate endophytic fungi species growth in weed seeds.     

Biosorption of Cr3+, Cd2+ and Cu2+ ions by blue-green algae Spirulina sp.: kinetics, equilibrium and the mechanism of the process

The process of biosorption of heavy metal ions (Cr3+, Cd2+, Cu2+) by blue-green algae Spirulina sp. is discussed in this paper. Spirulina sp. was found to be a very efficient biosorbent. The aim of the present study was to investigate quantitatively the potential binding sites present at the surface of Spirulina sp., using both potentiometric titrations and adsorption isotherms. The kinetic experiments showed that the process equilibrium was reached quickly, in less than 5-10 min. It was found that the equilibrium dependence between biosorption capacity and bulk metal ion concentration could be described with Langmuir equation. This suggests that the mechanism of biosorption is rather chemisorption than physical adsorption and was further confirmed by the low surface area associated with physical adsorption and by the presence of cations that appeared in the solution after biosorption. The maximum contribution of physical adsorption in the overall biosorption process was evaluated as 3.7%. It was proposed that functional groups on the cell surface contributed to the binding of metal ions by a biosorbent via equilibrium reaction. Three functional groups capable of cation exchange were identified on the cell surface. The biomass was described as weakly acidic ion exchanger. Since deprotonation of each functional group depends on pH, the process of biosorption is strongly pH-dependent. This was confirmed in the biosorption experiments carried out at different pH. The contribution of functional groups in the biosorption process was confirmed by chemical modification of the groups. Chemically blocked groups did not show neither biosorption nor ion-exchange capabilities. It has been shown that growth conditions can affect the metal adsorption properties of microalgae. The paper also discusses desorption characteristics of the biosorbent. The criteria for desorption were high elution efficiency and preservation of biosorptive properties. Desorbent that possessed these characteristics was nitric acid.     

Oxygen levels versus chemical pollutants: do they have similar influence on macrofaunal assemblages? A case study in a harbour with two opposing entrances

Generally, harbours are polluted zones characterised by low values of hydrodynamism and oxygen in the water column and high concentrations of pollutants in sediments. The harbour of Ceuta, North Africa, has an unusual structure; it is located between two bays connected by a channel, which increases the water movement and exchange in the harbour, maintaining moderate oxygen levels in the water-sediment interface. Nevertheless, high concentration of organic matter, nutrients and heavy metals were measured in sediments from this harbour. Under these unusual conditions (high levels of pollution but total saturation of oxygen in the water column) we studied the responses of soft-bottom macrobenthic communities using uni and multivariate analyses. The number of species was similar inside and outside the harbour but the species composition differed between internal and external stations; oxygen levels seem to control the "quantity" of species whereas pollutants control the "quality" of them.     

Pollution prevention and control procedure case study: an application for petroleum refineries

There is global environmental concern about the pollution from industries and other organizations that should not only be controlled but also prevented. Many alternatives are available to those in charge of environmental protection, but they should be able to draw on a systematic procedure to help implement prevention and control measures. At present, there are three immediate tasks: defining the objective of any environmental study, identifying the potential pollution sources, and selecting alternatives to these sources. However, it is necessary to evaluate these alternatives by using as large a number of criteria as possible and making them cumulative so as to enable the classification and selection of the best available techniques for each pollution source. The petroleum refining industry plays an important role in the developed economies and also has a potential for pollution generation that must be controlled. The best solution for all (i.e., petroleum companies, the public, and the environment) is pollution prevention, because this option will protect all of them and will also reduce costs in terms of lower raw materials consumption as well as reducing potential fines. The procedure we have presented in this article has been applied successfully.