Cost-effectiveness analysis of the seamistTM borehole liner system

SEAMIST^TM is an innovative technology that facilitates measurements of contaminants in both vertical and horizontal boreholes. The essence of SEAMIST^TM is an airtight membrane liner pneumatically emplaced inside the borehole and maintained with positive pressure. Sampling ports, absorbent collectors, and various in-situ measuring devices can be fabricated into the liner. Small instruments and cameras can be guided through the borehole to obtain real-time data. This article reports on the cost and performance effectiveness of this new technology. In this report, SEAMIST^TM is evaluated as a tool for obtaining data on volatile organic compounds, semivolatile organic compounds, other water-borne contaminants, and radionuclides. SEAMIST^TM is also compared to traditional borehole casing, to conventional soil vapor probes, and to conventional pore-fluid collecting lysimeters. The most cost- and performance-effective applications of SEAMIST^TM are shown to be those applications for which multiple characterization requirements can be combined into one SEAMIST^TM membrane system.     

Degradation and sorption of metribuzin and primary metabolites in a sandy soil

Leaching to the ground water of metabolites from the herbicide metribuzin [4-amino-6-(1,1-dimethylethyl)-3-(methylthio)-1,2,4-triazin-5-one] has been measured in a Danish field experiment in concentrations exceeding the European Union threshold limit for pesticides at 0.1 microg/L. In the present work, degradation and sorption of metribuzin and the metabolites desamino-metribuzin (DA), diketo-metribuzin (DK), and desamino-diketo-metribuzin (DADK) were studied in a Danish sandy loam topsoil and subsoil from the field in question, using accelerated solvent extraction and liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. Fast dissipation of metribuzin and the metabolites was observed in the topsoil, with 50% disappearance within 30 to 40 d. A two-compartment model described degradation of metribuzin and DA, whereas that of DADK could be described using first-order kinetics. Part of the dissipation was probably due to incorporation into soil organic matter. Degradation in subsoil occurred very slowly, with extrapolated half-lives of more than one year. Sorption in the topsoil followed the order DA > metribuzin > DK > DADK. Subsoil sorption was considerably lower, and was hardly measurable for metribuzin and DK. Abiotic degradation was considerably higher in the topsoil than the subsoil, especially concerning the de-amination step, indicating that organic matter may be related to the degradation process. The present results confirm observations of metribuzin and transformation product leaching made in the field experiment and demonstrate the need for knowledge on primary metabolites when assessing the risk for pesticide leaching.     

Levels and congener pattern of polychlorinated biphenyls in kittiwakes (Rissa tridactyla), in relation to mobilization of body-lipids associated with reproduction

Three groups of female kittiwakes (Rissa tridactyla) were collected in a North-Norwegian colony: (i) before breeding; (ii) immediately after egg-laying; and (iii) late in the chick-rearing period. Concentrations of 21 selected individual polychlorinated biphenyls (PCBs) were determined in liver, brain and fat tissues by capillary gaschromatography (GC-ECD). This was done in order to investigate how the mobilization of lipids associated with breeding influences concentrations and compositions of PCBs in these tissues. The results indicate an average decrease in body mass from pre-breeding to late chick-rearing of almost 20%. During this period, the mean concentration of PCBs in brain tissue approximately quadruples. This increase can be attributed to the redistribution of PCBs from utilized depot fat to metabolizing organs. A strong negative correlation was found between body mass and lipid weight PCB-concentrations in all three tissues. The relative amounts of different PCB-congeners were quite similar in different tissues, and showed only minor changes during the breeding period.     

Winter losses of nitrogen and phosphorus from Italian ryegrass, meadow fescue and white clover in a northern temperate climate

We have studied to what degree Italian ryegrass (Lolium multiflorum Lam.), white clover (Trifolium repens L.) and meadow fescue (Festuca pratensis L.) are able to preserve nitrogen (N) and phosphorous (P) in shoots and roots from one growing season to the next in a northern temperate climate. Field experiments were performed during four consecutive winters in central southeast Norway (60°42′N, 10°51′E), and N and P in plant biomass were measured in the autumn and in the spring. We also measured the contents of total N, total P and organic carbon (C) in seepage water that percolated through the aboveground plant material. Uptake of N and P in Italian ryegrass and white clover was substantially larger than in meadow fescue. The winter losses varied greatly from year to year, depending on the winter climate. On the average for all three of the plant species, the winter losses of N from aboveground biomass were 6, 35, 68 and 10% in the four experimental years, respectively. The corresponding P losses were 11, 36, 60 and 22%. On the average for all plant species and experimental years, 43 (±12)% (S.E., n = 12) of the N, 34 (±9)% of the P and 4 (±1)% of the C that was lost from the aboveground plant biomass during the winter, was recovered in seepage water, basically as a nutrient pulse in melt water in early spring. The very low C recovery rate in seepage water suggested a considerable microbial growth on lost plant C. Assuming that all un-recovered plant C was consumed by microorganisms not included in measurements of the seepage water, modelling showed that microbial immobilisation theoretically might explain the unexpectedly low recovery rates of N and P. The study was not designed to investigate the possible effects of psychrophilic microbes on N and P cycling. Therefore, it is inconclusive and underlines the need for more knowledge on this matter.     

Fate and transport of chlormequat in subsurface environments

Background, aim and scope  

Chlormequat (Cq) is a plant growth regulator used throughout the world. Despite indications of possible effects of Cq on mammalian health and fertility, little is known about its fate and transport in subsurface environments. The aim of this study was to determine the fate of Cq in three Danish subsurface environments, in particular with respect to retardation of Cq in the A and B horizons and the risk of leaching to the aquatic environment. The study combines laboratory fate studies of Cq sorption and dissipation with field scale monitoring of the concentration of Cq in the subsurface environment, including artificial drains.     

Triclosan affects the microbial community in simulated sewage-drain-field soil and slows down xenobiotic degradation

Effects of the common antibacterial agent triclosan on microbial communities and degradation of domestic xenobiotics were studied in simulated sewage-drain-field soil. Cultivable microbial populations decreased 22-fold in the presence of 4 mg kg⁻¹ of triclosan, and triclosan-resistant Pseudomonas strains were strongly enriched. Exposure to triclosan also changed the general metabolic profile (Ecoplate substrate profiling) and the general profile (T-RFLP) of the microbial community. Triclosan degradation was slow at all concentrations tested (0.33-81 mg kg⁻¹) during 50-days of incubation. Mineralization experiments (¹⁴C-tracers) and chemical analyses (LC-MS/MS) showed that the persistence of a linear alkylbenzene sulfonate (LAS) and a common analgesic (ibuprofen) increased with increasing triclosan concentrations (0.16-100 mg kg⁻¹). The largest effect was seen for LAS mineralization which was severely reduced by 0.16 mg kg⁻¹ of triclosan. Our findings indicate that environmentally realistic concentrations of triclosan may affect the efficiency of biodegradation in percolation systems.     

Analysis of acidic pesticides using in situ derivatization with alkylchloroformate and solid-phase microextraction (SPME) for GC-MS.

A solid-phase microextraction (SPME) method was developed for the analysis of acidic pesticide residues in water. The method utilizes in situ derivatization with butylchloroformate (BuCF), followed by on-line SPME extraction using a PDMS fibre, and analysis by GC-MS. Derivatives of the phenoxy acids mechlorprop (MCPP), dichlorprop (DCPP), MCPA and 2,4-D and their phenol degradation products 4-chloro-2-methylphenol and 2,4-dichlorophenol (DCP) were identified. Detection limits at 0.16-2.3 microg/l were achieved. Optimization of derivatization, ion strength, extraction time, SPME-fibre, desorption time and temperature are described. Standard curves in the range 0.5-10.0 microg/l were fitted to a second-degree polynomial. Standard deviation (n = 5) was below 10% for the phenol derivatives, but 20-50% for the phenoxy acids. For method verification groundwater samples from a field experiment were screened for content of MCPP and compared to the results from the HPLC analysis. A good agreement was obtained with respect to identification of positive samples, even though concentrations measured by the SPME were lower than with HPLC. Even if the precision and accuracy do not meet the demands for a strictly quantitative analysis, the SPME method is suitable for screening, because it is cheap, it can be automated, and uses smaller amounts of potential harmful solvents. Also, the method is less labour-intensive, as it requires a minimum of sample preparation when compared to traditional analyses. The acidic pesticides bentazon, dicamba, bromoxynil, ioxynil, dinoseb and DNOC were included in the study but could not be analysed by the current method.