Comparative persistence of marine fish larvae from pelagic versus demersal eggs off southwestern Nova Scotia,Canada

Two groupings of larval fish were repeatedly identified by principal component analyses of larval densities from four broad-scale surveys during the spring and summer of 1985–1987 off southwestern Nova Scotia, Canada. Larvae originating from pelagic eggs (four species within Gadidae and Pleuronectidae) constituted one group, which were uniformly distributed over the sampling area with densities not correlated with bathymetry, although nearly all spawning occurs on the shallow western cap of Browns Bank, 100 km offshore. Larvae from demersal eggs (five species within Pholidae, Stichaeidae, Cottidae, Agonidae) constituted the second group, which dominated the shallow-water environments both inshore and on Browns Bank. Lower patchiness indices were evident amongst larvae from pelagic eggs in small and large sampling-gear collections (average 3.4 and 3.1, respectively) compared to fish hatching from demersal eggs (average 5.1 and 4.6). Fine-scale nearshore surveys over a 5 wk period in 1987 also showed that larvae of demersal eggs had a less variable distribution along an inshoreoffshore transect. Larvae from demersal eggs appear spatially persistent through the release of well-developed larvae from non-drifting eggs. These conclusions are consistent with other studies over a range of spatial scales in temperate and tropical environments, demonstrating that single-species models of larval dispersal are inadequate to account for the distributional patterns of larval fish in general.     

Semicontinuous PM2.5 sulfate and nitrate measurements at an urban and a rural location in New York: PMTACS-NY summer 2001 and 2002 campaigns

Several collocated semicontinuous instruments measuring particulate matter with particle sizes < or =2.5 microm (PM2.5) sulfate (SO4(2-)) and nitrate (NO3-) were intercompared during two intensive field campaigns as part of the PM2.5 Technology Assessment and Characterization Study. The summer 2001 urban campaign in Queens, NY, and the summer 2002 rural campaign in upstate New York (Whiteface Mountain) hosted an operation of an Aerosol Mass Spectrometer, Ambient Particulate Sulfate and Nitrate Monitors, a Continuous Ambient Sulfate Monitor, and a Particle-Into-Liquid Sampler with Ion Chromatographs (PILS-IC). These instruments provided near real-time particulate SO4(2-) and NO3- mass concentration data, allowing the study of particulate SO4(2-)/NO3- diurnal patterns and detection of short-term events. Typical particulate SO4(2-) concentrations were comparable at both sites (ranging from 0 to 20 microg/m3), while ambient urban particulate NO3- concentrations ranged from 0 to 11 microg/m3 and rural NO3- concentration was typically less than 1 microg/m3. Results of the intercomparisons of the semicontinuous measurements are presented, as are results of the comparisons between the semicontinuous and time-integrated filter-based measurements. The comparisons at both sites, in most cases, indicated similar performance characteristics. In addition, charge balance calculations, based on major soluble ionic components of atmospheric aerosol from the PILS-IC and the filter measurements, indicated slightly acidic aerosol at both locations.     

Designing monitoring networks to represent outdoor human exposure

Measurements of outdoor human exposure to suspended particulate matter (PM) are always constrained by available resources. An effective network design requires tradeoffs between variables measured, the number of sampling locations, sample duration, and sampling frequency. Sampling sites are needed to represent neighborhood and urban spatial scales with minimal influences from nearby sources. Although most PM measurements for determining compliance with standards are taken over 24-h periods every third to sixth day, outdoor human exposure assessment requires measurements taken continuously throughout the day, preferably over durations of 1 h or less. More detailed particle size and chemistry data are also desirable, as smaller size fractions and specific chemicals may be better indicators of adverse health effects than total mass samples.     

Formation and emission of chloroanisoles as indoor pollutants

GOAL, SCOPE AND BACKGROUND: Complaints by residents of frame-houses about musty odour in the houses has become an increasing problem within the last years. An additional problem is that the odour is transferred to clothes and skin. The persons themselves do not recognize the smell after a while because of adaptation. Serious social problems are the result. For a long time, the smell was explained to be from mould due to construction-based humidity problems. However, in an increasing number of houses, no indications were found for elevated levels of mould growth. METHODS: Air and material samples were taken from 5 houses, which show typical musty odours, and analysed with respect to chlorophenols and chloroanisoles. Additionally, some samples were analysed for lindane and its metabolites, because lindane was commonly used together with pentachlorophenol (PCP) for wood protection. RESULTS AND DISCUSSION: Meticulous analysis resulted in the identification of chloroanisoles, mainly 2,3,4,6-tetrachloroanisole. These substances are known from corky wines and from contamination of food from pentachlorophenol (PCP) treated pallets and result from microbiological metabolic processes. Pentachlorophenol was commonly used to protect wood from fungi in Germany mainly in the later 60s and 70s. Details of these processes, as well as effective methods to identify chloroanisoles in the problem houses, are described. CONCLUSIONS: Chloroanisoles formed by metabolism of PCP have been well known to contaminate food or wine. Here, they were identified and are probably responsible for the musty odours in the frame houses. Since it is quite clear that these substances were not components of building materials used in the houses, an explanation for chloroanisole formation is proposed. Localized dampness probably favours microbial growth associated with metabolic conversion of chlorophenols to the corresponding chloroanisoles, primarily 2,3,4,6-tetrachloroanisol, which spread throughout the buildings, resulting in the observed odours. RECOMMENDATIONS AND OUTLOOK: The group of chloroanisoles has been recognized as important indoor pollutants as they possess musty odours at extremely low concentrations, e.g. for 2,4,6-trichloroanisole in a range of 5-10 ppt in air (Staples 2000). On the basis of currently available toxicological data, exposure of the occupants to the concentrations of chloroanisoles measured is not associated with a health risk. No correlation could be observed between concentrations of chloroanisoles and PCP in house dust and indoor air. However, chloroanisoles are good indicators for possible PCP-treatment of wood in frame houses and their detection should initiate investigations on PCP contamination. Research is continuing to identify the microorganisms involved and to devise a remediation procedure for affected houses.     

Analysis of microbiological screen test data for antimicrobial residues in food animals

This study analyzes the National Residue Program (NRP) of the Food Safety and Inspection Service (FSIS), United States Department of Agriculture (USDA), data for the years 1983-1998 to determine the effectiveness of all three microbiological screen tests that were developed and used by the FSIS to control antimicrobial residues in food animals. The Swab Test On Premises (STOP) was the first screen test introduced in slaughterhouses, followed by the Calf Antibiotic Sulfonamide Test (CAST) and the Fast Antimicrobial Screen Test (FAST). The data for STOP indicates that during 1983-1998, the rate of food animal carcasses with violative levels of antimicrobial residues reduced from 2.33% to 0.45% under the monitoring plan and under the surveillance plan, the rate reduced from 55.1% to 0.56%. Similarly, the data for CAST indicates that the rate of calf carcasses with violative levels of antimicrobial residue also declined significantly during those years. Because of its higher sensitivity and shorter analytical time, the use of FAST started in 1995. By 1999, it had practically replaced the use of STOP and CAST in bovine species. The use of only one test such as FAST instead of different tests has removed confusion for testing different species of food animals and thereby has enhanced the efficiency of the NRP.     

Determination of mutagenic potential and organic contaminants of Great Lakes drinking water

Extracts of organic compounds were obtained, using XAD-2 macroreticular resin, from drinking water supplies in 12 Great Lakes municipalities. The extracts were tested for mutagenic potential using the Salmonella/mammalian-microsome assay and analysed for organochlorine pesticides, polyaromatic hydrocarbons, organophosphorous pesticides and trialkyl-arylphosphates. Grab samples of drinking water were also analysed for volatile organic compounds. Dose-related increases in mutagenicity were found in extracts from 11 of the drinking water supplies.     

Influence of aeration rate and reactor shape on the composting of poultry manure and sawdust

To achieve successful composting, all the biological, chemical, and physical characteristics need to be considered. The investigation of our study was based on various physicochemical properties, i.e., temperature, ammonia concentration, carbon dioxide concentration, pH, electrical conductivity (EC), carbon/nitrogen (C/N) ratio, organic matter (OM) content, moisture content, bacterial population, and seed germination index (GI), during the composting of poultry manure and sawdust for different aeration rates and reactor shapes. Three cylindrical-shaped and three rectangular-shaped pilot-scale 60-L composting reactors were used in this study, with aeration rates of 0.3 (low), 0.6 (medium), and 0.9 (high) L min^?1 kg^?1 DM (dry matter). All parameters were monitored over 21 days of composting. Results showed that the low aeration rate (0.3 L min^?1 kg^?1 DM) corresponded to a higher and longer thermophilic phase than did the high aeration rate (0.9 L min^?1 kg^?1 DM). Ammonia and carbon dioxide volatilization were directly related to the temperature profile of the substrate, with significant differences between the low and high aeration rates during weeks 2 and 3 of composting but no significant difference observed during week 1. At the end of our study, the final values of pH, EC, moisture content, C/N ratio, and organic matter in all compost reactors were lower than those at the start. The growth rates of mesophilic and thermophilic bacteria were directly correlated with mesophilic and thermophilic conditions of the compost. The final GI of the cylindrical reactor with an airflow rate of 0.3 L min^?1 kg^?1 DM was 82.3%, whereas the GIs of the other compost reactors were below 80%. In this study, compost of a cylindrical reactor with a low aeration rate (0.3 L min^?1 kg^?1 DM) was more stable and mature than the other reactors.

Implications: The poultry industry is growing in South Korea, but there are problems associated with the management of poultry manure, and composting is one solution that could be valuable for crops and forage if managed properly. For high-quality composting, the aeration rate in different reactor shapes must be considered. The objective of this study was to investigate various physicochemical properties with different aeration rates and rector shapes. Results showed that aeration rate of 0.3 L min^?1 kg^?1 DM in a cylindrical reactor provides better condition for maturation of compost.     

Peatlands: a major sink of naturally formed organic chlorine

It is a little known fact that many chlorinated organic compounds occur naturally and that some are also indispensable to life on earth. Here, we show that chlorination of organic compounds during humification processes in peat is widespread in nature. Globally this process has led to the accumulation of approximately 280-1000 million tons of organically bound chlorine in peatlands during the postglacial period.     

Remediation of BTEX and trichloroethene

The widespread use of industrial chemicals in our highly industrialized society has often caused contamination of large terrestrial and marine areas due to the deliberate and accidental release of organic pollutants into the soil and groundwater. In this review, environmental problems arising from the use of chlorinated solvents and BTEX compounds are described, and an overview about active management strategies for remediation with special emphasis on phytoremediation are presented to achieve a reduction of the total mass of chlorinated solvents and BTEX compounds in contaminated areas. Phytoremediation has been proposed as an efficient, low-cost remediation technique to restore areas contaminated with chlorinated solvents and BTEX compounds. The feasibility of phytoremediation as a remediation tool for these compounds is discussed with particular reference to the uptake and metabolism of these compounds, and a future perspective on the use of phytoremediation for the removal of chlorinated solvents and BTEX compounds is given.     

Investigation of selective catalytic reduction impact on mercury speciation under simulated NOx emission control conditions

Selective catalytic reduction (SCR) technology increasingly is being applied for controlling emissions of nitrogen oxides (NOx) from coal-fired boilers. Some recent field and pilot studies suggest that the operation of SCR could affect the chemical form of mercury (Hg) in coal combustion flue gases. The speciation of Hg is an important factor influencing the control and environmental fate of Hg emissions from coal combustion. The vanadium and titanium oxides, used commonly in the vanadia-titania SCR catalyst for catalytic NOx reduction, promote the formation of oxidized mercury (Hg2+). The work reported in this paper focuses on the impact of SCR on elemental mercury (Hg0) oxidation. Bench-scale experiments were conducted to investigate Hg0 oxidation in the presence of simulated coal combustion flue gases and under SCR reaction conditions. Flue gas mixtures with different concentrations of hydrogen chloride (HCl) and sulfur dioxide (SO2) for simulating the combustion of bituminous coals and subbituminous coals were tested in these experiments. The effects of HCl and SO2 in the flue gases on Hg0 oxidation under SCR reaction conditions were studied. It was observed that HCl is the most critical flue gas component that causes conversion of Hg0 to Hg2+ under SCR reaction conditions. The importance of HCl for Hg0 oxidation found in the present study provides the scientific basis for the apparent coal-type dependence observed for Hg0 oxidation occurring across the SCR reactors in the field.