Measurement of watershed phosphorus: A review

Eutrophication control programs are based on phosphorus management which, in turn, requires a detailed quantification of the watershed phosphorus budget. This involves an assessment of non‐point sources of phosphorus, a key element of which is determining the fraction of soil‐P and sediment‐P available to support algal growth. This paper presents a review of the state‐of‐the‐art of estimating algal available‐P from non‐point sources, and an analysis of pertinent data. The need to employ multi‐interval algal bioassays in developing phosphorus management systems is stressed.     

Voltammetric studies of damages in DNA by mutagenic and carcinogenic alkylating chemicals

Voltammetry provides new insights into the effects exerted in vitro by methylation of native DNA. Applying single sweep voltammetry at a stationary mercury electrode the successive steps of the destabilization of alkylated DNA are investigated. The methylation of the nucleic acids is manifested by a specific electrochemical response, due to the 7‐methylguanine, a major product of the methylation of DNA. Short time effects of the methylation include the labilization of 4 to 5 base pairs per methylated guanine base. Furthermore, uncommon protonation properties of the base 7‐methylguanine‐cytosine have been detected. Long term effects of the methylation are ultimately spontaneous hydrolytic strand breaks induced by the prior depurination connected with the release of the 7‐methylguanine from the methylated DNA. A half time t_1/2 of 102 h for the depurination at 37°C has been determined. The depurination and the subsequent strand breaks alter the hydrodynamic properties of the damaged DNA, an effect which can be sensitively followed with voltammetry via the resulting changes in the diffusion coefficient of the damaged biopolymer.     

Influence of phytoplankton on complexing capacity of seawater†

Differential Pulse Anodic Stripping Voltammetry (DPASV) was employed to measure Apparent Copper Complexing Capacity (L_t) and Stability Constants (K_s) of related cupric complexes of cell exudates of the phytoplanktonic alga Dunaliella salina. Three natural seawater samples collected 0.1, 2, 5 miles off the Tyrrhenian coast were used as culture medium. The measurements were carried out 1h and 7 days after the inoculum. Furthermore, on one culture the medium was passed through C₁₈‐SEP‐PAK cartridges in order to separate the cell exudates. The results show that Dunaliella salina influences the value of L_t but does not affect the value of K_s . The C₁₈SEP‐PAK retain only 50% of the ligands produced by the cells and capable of complexing copper.     

Sea water quality monitoring in Rhodes and Cos (Greece)

During the years 1983–1986, a program aiming at monitoring water quality of the most crowded beaches, as well as assessing and minimizing pollution from certain land based sources was carried out in Rhodes and Cos. The program was directed towards inspections of treatment plants as well as laboratory analyses of treated effluents from large hotels. As a result, almost one in four hotels was obliged to construct a new treatment plant. In order to help personnel to improve plant efficiency through day‐to‐day maintenance a three day seminar was held in June 1985. Sea water quality parameters (total coliforms and E. coli) were found to be well below the limits set by E.E.C. directives.     

Polarographic investigations on the complexation of cadmium and zinc by thiol peptides

Complex formation of Cd²⁺ and Zn²⁺ with thiol derivatives has been investigated by differential pulse polarography. The binding of Cd²⁺ and Zn²⁺ with cysteine (CySH), glutathione (GSH) and the model peptide N‐acetyl‐cysteine‐methylamide (ASH) reveals different stoichiometry. Thus, Cd²⁺ forms 1:1 and 1:2 complexes with CySH while 1:2 and 1:4 complexes have been observed with GSH and ASH, respectively. Overall formation constants of Cd²⁺ with CySH (Iogβ ₂ 15.3) and with GSH (Iogβ5₂ 14.4) have been estimated using competitive complexation with nitrilotriacetic acid (NTA). Investigation of competition between Zn²⁺ and Cd²⁺ for the thiol complexation has underlined the role played by the amino group in CySH for the stabilization of Zn complexes in contrary to Cd complexes.     

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.     

Singlet molecular oxygen—mediated photooxidation of monochloro and mononitrophenols. A kinetic study

A kinetic and mechanistic study on the aerobic dye sensitized photooxidation of the mono—nitro and chlorophenols was carried out. A singlet molecular oxygen mechanism operates in the photooxidation. Solvent and substituent effects, suggest the intermediacy of a complex with partial charge transfer character, as has been postulated for other phenols.

Chemical (reactive) and physical interactions of the substrates with singlet molecular oxygen were discriminated. Quantum yields for photooxidation (higher for the chlorophenols) range from 3 × 10^‐2 to 2 × 10^‐3, as measured by substrate or oxygen consumption. These values indicate the viability of a singlet molecular oxygen photooxidation as a way for the degradation of nitro and chlorophenol environmental contaminants.     

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..     

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.