Development of environmental policy,objectives, and targets

This paper describes a process to develop and establish an environmental policy and its associated environmental targets, objectives, and management programmes. The environmental policy is defined in a statement which addresses the company expectations for programmes that are important to assure adequate environmental protection and define its future commitment towards preventing pollution and continuously improving the effectiveness of its environmental protection programmes. A set of environmental objectives, derived from the policy, define the overall goals which will ensure that the company's environmental performance will remain consistent with the commitment identified in its policy when its environmental management system (EMS) is implemented, Environmental targets reflect the requirements and standards that the company must strive to achieve each objective and minimize any harmful environmental impacts from its production and manufacturing processes or other activities. In addition to defining specific targets, environmental management programmes are also used to guide EMS implementation. These programmes, however, must provide the company with the necessary flexibility to select the most appropriate technologies to enhance its own processes and prudently allocate its available financial resources in areas that return the greatest overall environmental benefit.Though they are expected to allow some discretion in the allocation of resources targeted towards environmental protection, EMS programmes must also provide assurance that the corporation environmental policy, objectives, targets, and management programmes do not result in a facility failure to adhere to all of its certification requirements. The principle and factors described in this article should be considered to the extent that they are necessary and practical.     

Suspension and resuspension of dry soil indoors following track-in on footwear

Contamination of the indoor environment by tracked-in outdoor soil has the potential to pose a significant human health threat through exposure to hazardous soil constituents. The indoor distribution of (contaminated) soil following ingress is important when evaluating exposure risk. Here, the time evolution of size-resolved airborne particulate matter aerosolized as a result of mechanical (i.e., footfall or step-on) impacts on a floor surface with a layer of dry soil was investigated using laser particle counters. Suspended particle levels were recorded after step-on impacts that aerosolized soil particles at a single contact point by the action of a human tester who followed a pre-determined walking pattern. The experimental design presumed that the floor area immediately upon entrance indoors is the location of maximum deposition of outdoor soil transferred on footwear. The suspension of soil resulting from the first step-on floor contact and the subsequent resuspension of soil resulting from additional step-on events were quantified by various arrangements of four laser particle counters. Step-on impacts produced a transient increase in particle levels at various lateral distances and heights from the contact point. Also, with increasing distance and height from the step-on contact point, the level of suspended particles after successive step-on events decreased markedly. The results suggested that a lateral component of the dispersion process was more significant than a vertical one under these experimental conditions. A wall jet effect created by the impact of the footfalls on the floor surface was considered responsible for the apparent greater lateral dispersion of the soil particles.     

Analytical solutions for flow induced by a vertically distributed turbulent plume

Environmental Fluid Mechanics - Analytical solutions are developed for the flow induced by a vertically distributed turbulent plume in an otherwise quiescent uniform environment. The plume...     

Ammonia volatilization from marsh-pond-marsh constructed wetlands treating swine wastewater

Ammonia (NH3) volatilization is an undesirable mechanism for the removal of nitrogen (N) from wastewater treatment wetlands. To minimize the potential for NH3 volatilization, it is important to determine how wetland design affects NH3 volatilization. The objective of this research was to determine how the presence of a pond section affects NH3 volatilization from constructed wetlands treating wastewater from a confined swine operation. Wastewater was added at different N loads to six constructed wetlands of the marsh-pond-marsh design that were located in Greensboro, North Carolina, USA. A large enclosure was used to measure NH3 volatilization from the marsh and pond sections of each wetland in July and August of 2001. Ammonia volatilized from marsh and pond sections at rates ranging from 5 to 102 mg NH3-N m(-2) h(-1). Pond sections exhibited a significantly greater increase in the rate of NH3 volatilization (p < 0.0001) than did either marsh section as N load increased. At N loads greater than 15 kg ha(-1) d(-1), NH3 volatilization accounted for 23 to 36% of the N load. Furthermore, NH3 volatilization was the dominant (54-79%) N removal mechanism at N loads greater than 15 kg ha(-1) d(-1). Without the pond sections, NH3 volatilization would have been a minor contributor (less than 12%) to the N balance of these wetlands. To minimize NH3 volatilization, continuous marsh systems should be preferred over marsh-pond-marsh systems for the treatment of wastewater from confined animal operations.     

Retention of nitrogen and phosphorous from liquid swine and poultry manures using highly characterized peats

This paper reports on research designed to test the hypothesis that differences in peat composition will cause differences in amounts of N and P retained during contact with liquid swine manure (LSM) and liquid poultry manure (LPM). Peat types representing a wide range of properties were tested in order to establish which chemical and physical properties might be most indicative of their capacities to retain N and P from LSM and LPM. Eight-percent slurries (peat/LSM and peat/LPM) were measured for total nitrogen (TKN) and total phosphorous (TP) after 6, 24 and 96 hours. Tests were done to determine the TKN and TP contents of these peats, the LSM, and the LPM, both before and after they were mixed together. The N and P retention results revealed that most peats worked reasonably well at retaining N and P from either LSM or LPM. However, some peats were more effective than others. These peats also decreased the N and P levels in the liquid portion of the LSM. Peats with higher N retention capacities tended to have lower ash contents, but higher macroporosities and total cellulose contents. Peats with higher P retention capacities tended to have lower bulk densities, ash contents, total guaiacyl lignins contents, fulvic acids contents, but higher microporosities, macroporosities, H contents, and total cellulose contents. Peats with higher N and P retention capacities also had humic acid contents between 5-7%. The results of this study suggest that if these peats are used to reduce odors and N and P contamination, possible byproducts could be the production of odorless fertilizers.     

Overview of regulatory/policy/economic issues related to carbon dioxide

This is an overview of Session 2c dealing with the regulatory, policy and economic issues related to carbon dioxide and its impact on global climate change. The information is taken from the two papers presented in this session (the U.S. Perspective by Dennis Leaf and the European Perspective by Hans J.H. Verolme) and from the panel discussion that took place at the end of the session. The overview focuses primarily on the policy responses of both the United States (US) and the United Kingdom (UK) to changes in global atmospheric pollution. To a lesser extent, the progress of policy responses to these changes is discussed. The United Nations Framework Convention on Climate Change (UNFCCC) has been signed and ratified by over 180 countries. The UNFCCC contained no binding targets or timetables for emissions reductions. The Kyoto Protocol [United Nations. Kyoto Protocol to the United Nations Framework Convention on Climate Change. UNEP.IUC/99/10. Chatlelaine, Switzerland: United Nations Environment Programme's Information Unit for Conventions, for the Climate Change Secretariat, 1997] to the UNFCCC did contain targets and timetables for reductions of greenhouse gases on the part of developed countries. The US has signed but not ratified the Kyoto Protocol. The US has experienced some movement to reduce greenhouse gas emissions on the part of various levels of government, as well as the private sector. The UK's commitment to reducing green house gases is laid down in the UK Climate Change Programme 2000. The UK is a member of the European Union (EU). In this context, an example of EU-wide progress, the voluntary agreement with car manufacturers to reduce CO(2) emissions in new vehicles, will be discussed. In addition, there will be some discussion on the UK CO(2) trading scheme that created the first market in the world in April 2001. Overall, the policy process is constantly informed by scientific research. In the case of climate change, much of this work is carried out under the auspices of international scientific panels.     

THE DEVELOPMENT AND IMPLEMENTATION OF A GIS-BASED CONTAMINANT SOURCE INVENTORY OVER THE SPOKANE AQUIFER,SPOKANE COUNTY WASHINGTON1

ABSTRACT: U.S. Environmental Protection Agency (EPA) statutes require identification of all potential sources of contamination within a wellhead protection area. All wells over Spokane County's aquifer are included in one wellhead protection zone called the Aquifer Sensitive Area (ASA). A GIS-based Contaminant Source Inventory (CSI) was developed for the ASA. Datasets listing businesses and agencies within the ASA were imported into the GIS from state, county, city, and local agencies. These datasets were selected, joined, and sorted using GIS relational database capabilities into one ASA “business master file.” Map files were projected and transformed into common coordinates. Next, business sites within the master file were spatially related by address to the digital map files. Likely Critical Materials Users (CMU) were identified by sorting on selected standard Industrial Codes (SIC). Additional files of CMUs were imported into the Contaminant Source Inventory. GIS queries were performed to locate specific materials, quantities, and storage facilities, and to analyze CMU activity within selected buffer zones. This project demonstrated the usefulness of GIS technology in the development, management, maintenance, and analysis of vast quantities of data associated with a local wellhead protection pro. gram.     

Discrimination of flicker frequency rates in the reptile tuatara (Sphenodon )

By investigating the mechanisms that underlie the perception of environmental cues, we may begin to understand how the sensory system governs behavioral responses. This is the first empirical study to examine learning and visual sensitivity in a reptile species, the tuatara (Sphenodon punctatus). We established a non-intrusive psychophysical method by employing an instrumental paradigm in order to examine discrimination learning and the ability to distinguish different flicker frequencies in the tuatara. Seventeen tuatara were trained under an operant conditioning task to respond to various discriminative stimuli flickering between 2.65 and 65.09 Hz. Tuatara were able to learn the operant task and discriminate between a constant light and flicker frequency rates between 2.65 and 45.61 Hz, but not at 65.09 Hz. We demonstrated a reliable psychophysical method where these reptiles could learn a basic operant task and discriminate visual stimuli in the form of flicker frequency rates. The tuatara’s ability to perceive flickering light is comparable to that of avian, mammalian, and other reptilian species. This method is thus suitable for more comprehensive examinations of vision and additional sensory abilities in other reptiles. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Risk remaining from fine particle contaminants after vacuum cleaning of hard floor surfaces

In the indoor environment, settled surface dust often functions as a reservoir of hazardous particulate contaminants. In many circumstances, a major contributing source to the dust pool is exterior soil. Young children are particularly susceptible to exposure to both outdoor derived soil and indoor derived dust present in the indoor dust pool. This is because early in life the exploratory activities of the infant are dominated by touching and mouthing behavior. Inadvertent exposure to dust through mouth contact and hand-to-mouth activity is an inevitable consequence of infant development. Clean-up of indoor dust is, in many circumstances, critically important in efforts to minimize pediatric exposure. In this study, we examine the efficiency of vacuum cleaner removal of footwear-deposited soil on vinyl floor tiles. The study utilized a 5 × 10 foot (c. 152.5 × 305 cm) test surface composed of 1-foot-square (c. 30.5 × 30.5 cm) vinyl floor tiles. A composite test soil with moderately elevated levels of certain elements (e.g., Pb) was repeatedly introduced onto the floor surface by footwear track-on. The deposited soil was subsequently periodically removed from randomly selected tiles using a domestic vacuum cleaner. The mass and loading of soil elements on the tiles following vacuuming were determined both by wet wipe collection and by subsequent chemical analysis. It was found that vacuum cleaner removal eliminated much of the soil mass from the floor tiles. However, a small percentage of the mass was not removed and a portion of this residual mass could be picked up by moistened hand-lifts. Furthermore, although the post-vacuuming tile soil mass was sizably reduced, for some elements (notably Pb) the concentration in the residual soil was increased. We interpret this increased metal concentration to be a particle size effect with smaller particles (with a proportionately higher metal content) remaining in situ after vacuuming.