Measurement of transferable chemical residue from nylon carpet using the California roller and a new mega-California roller

Human chemical exposures resulting from transfer of surface deposition on indoor nylon carpets may be estimated by measuring transferable residues (mu g chemical/cm2 carpet). A weighted roller developed at California Department of Food and Agriculture (CDFA) has been extensively used to sample transferable residue for estimates of human exposure in risk characterization. A modified roller has been developed to evaluate the influence of pressure on transferable chemical residue since weight and force (or pressure, kg/m2) may vary person-to-person and activity-to-activity. A 30.5 cm diameter roller was used to apply 60 to 2100 kg/m2 to bracket pressures exerted by humans on a flat nylon-carpeted surface. Measurements of transferable cyfluthrin residues were made after 1, 7, and 21 days. Total Soxhlet extractable cyfluthrin residues were relatively constant during the test period. Residue transferability decreased during the study period. Modest increases in the transferability of surface residues were observed over the broad range of pressures applied by the modified roller.     

评估可离子化有机化合物的生物累积潜力：当前的认知和研究的重点

本研究的目的是回顾目前关于可离子化有机化合物(IOCs)的生物累积潜力的认知,重点讨论鱼类经验数据的有效性。IOCs在鱼体内的生物积累潜力可以很好地表征为：依赖pH的鳃摄取和排泄,肠道吸收和磷脂吸附(膜-水分区)。关键的挑战包括缺乏关于IOCs生物转化和血浆结合的经验数据。鱼拥有多种蛋白质,可以在细胞膜上传输IOCs。然而,除了少数情况下,这种传输对环境污染物的吸收和积累的意义是未知的。本文提出了2个研究案例。第一个描述了pH值和生物转化对有机酸和碱的生物富集的建模作用,而第二个则采用了一个更新的模型来研究导致全氟烷基酸积累的因素。全氟化烷基酸个案研究是值得关注的,因为它说明了膜转运蛋白在肾脏中可能具有的重要性,并强调了交叉比对方法(read-across approaches)的潜在价值。认识到当前需要对IOCs进行生物累积危害评估和生态风险评估,作者提供了一个分层策略,从保守的假设(模型和相关数据)到需要化学特定信息的更复杂的模型。
精选自Armitage, J. M., Erickson, R. J., Luckenbach, T., Ng, C. A., Prosser, R. S., Arnot, J. A., Schirmer, K. and Nichols, J. W. (2017), Assessing the bioaccumulation potential of ionizable organic compounds: Current knowledge and research priorities. Environmental Toxicology and Chemistry, 36: 882–897. doi: 10.1002/etc.3680
详情请见http://onlinelibrary.wiley.com/doi/10.1002/etc.3680/full
     

SWATMOD‐Prep: Graphical User Interface for Preparing Coupled SWAT‐MODFLOW Simulations

This article presents SWATMOD‐Prep, a graphical user interface that couples a SWAT watershed model with a MODFLOW groundwater flow model. The interface is based on a recently published SWAT‐MODFLOW code that couples the models via mapping schemes. The spatial layout of SWATMOD‐Prep guides the user through the process of importing shape files (sub‐basins, hydrologic response units [HRUs], river network) from an existing SWAT model, creating a grid, performing necessary geo‐processing operations to link the models, writing out SWAT‐MODFLOW files, and running the simulation. The option of creating a new single‐layer MODFLOW model for near‐surface alluvial aquifers is available, with the user prompted to provide groundwater surface elevation (through a digital elevation model), aquifer thickness, and necessary aquifer parameter values. The option of simulating nitrate transport in the aquifer also is available, using the reactive transport model RT3D. The interface is in the public domain. It is programmed in Python, with various software packages used for geo‐processing operations (e.g., selection, intersection of rasters) and inputting/outputting data, and is written for Windows. The use of SWATMOD‐Prep is demonstrated for the Little River Experimental Watershed, Georgia. SWATMOD‐Prep and SWAT‐MODFLOW executables are available with an accompanying user's manual at: http://swat.tamu.edu/software/swat-modflow/ . The user's manual also accompanies this article as Supporting Information.     

Measuring landscape integrity (LI): development of a hybrid methodology for planning applications

Landscape integrity data-sets represent a measure of a landscape's naturalness, or its inverse, the level of human modification. Generally referred to as human footprint modeling, a hybrid approach was developed here by incorporating distance, density, and spatially explicit fuzzy logic methods for quantifying the impacts of anthropocentric infrastructure on the landscape. Integrity scores varied markedly across this large and heterogeneous landscape. A comparative analysis among peer data products revealed that this model exhibited the highest level of correlation when compared to an independently derived expert survey of expected scores. Moreover, differences in correlation were found to be statistically significant in two cases indicating robust model performance. Data products such as these may be leveraged to quantify the nature and extent of human modifications on the landscape, identify highly natural areas for conservation purposes, and may serve as an overarching umbrella for guiding and coordinating large and local-scale planning efforts.     

The influence of nitrate on selenium in irrigated agricultural groundwater systems

Selenium (Se) contamination of groundwater is an environmental concern especially in areas where aquifer systems are underlain by Se-bearing geologic formations such as marine shale. This study examined the influence of nitrate (NO?) on Se species in irrigated soil and groundwater systems and presents results from field and laboratory studies that further clarify this influence. Inhibition of selenate (SeO?) reduction in the presence of NO? and the oxidation of reduced Se from shale by autotrophic denitrification were investigated. Groundwater sampling from piezometers near an alluvium-shale interface suggests that SeO? present in the groundwater was due in part to autotrophic denitrification. Laboratory shale oxidation batch studies indicate that autotrophic denitrification is a major driver in the release of SeO? and sulfate. Similar findings occurred for a shale oxidation flow-through column study, with 70 and 31% more reduced Se and S mass, respectively, removed from the shale material in the presence of NO? than in its absence. A final laboratory flow-through column test was performed with shallow soil samples to assess the inhibition of SeO? reduction in the presence of NO?, with results suggesting that a concentration of NO? of approximately 5 mg L or greater will diminish the reduction of SeO?. The inclusion of the fate and transport of NO? and dissolved oxygen is imperative when studying or simulating the fate and transport of Se species in soil and groundwater systems.     

Chemical and Biological Characterization of Products of Incomplete Combustion from the Simulated Field Burning of Agricultural Plastic

Chemical and biological analyses were performed to characterize products of Incomplete combustion emitted during the simulated open field burning of agricultural plastic. A small utility shed equipped with an air delivery system was used to simulate pile burning and forced-air-curtain incineration of a nonhalogenated agricultural plastic that reportedly consisted of polyethylene and carbon black. Emissions were analyzed for combustion gases; volatile, semi-volatile, and particulate organics; and toxic and mutagenlc properties. Emission samples, as well as samples of the used (possibly pesticide-contaminated) plastic, were analyzed for the presence of several pesticides to which the plastic may have been exposed. Although a variety of alkanes, alkenes, and aromatic and polycyclic aromatic hydrocarbon (PAH) compounds were identified in the volatile, seml-volatlle, and particulate fractions of these emissions, a substantial fraction of higher molecular weight organic material was not identified. No pesticides were Identified in either combustion emission samples or dlchloromethane washes of the used plastic. When mutagenlcity was evaluated by exposing Salmonella bacteria (Ames assay) to whole vapor and vapor/partlculate emissions, no toxic or mutagenlc effects were observed. However, organic extracts of the particulate samples were moderately mutagenlc. This mutagenlcity compares approximately to that measured from residential wood heating on a revertant per unit heat release basis. Compared to pile burning, forced air slightly decreased the time necessary to burn a charge of plastic. There was not a substantial difference, however, in the variety or concentrations of organic compounds Identified In samples from these two burn conditions. This study highlights the benefits of a combined chemical/biological approach to the characterization of complex, multi-component combustion emissions. These results may not reflect those of other types of plastic that may be used for agricultural purposes, especially those containing halogens.     

The Validation of a Passive Sampler for Indoor and Outdoor Concentrations of Volatile Organic Compounds

Abstract

Volatile organlcs compounds (VOCs) are ubiquitous in the air we breathe. The use of passive samplers to measure these concentrations can be an effective technique. When exposed for long durations, a passive sampler may be a good tool for investigating chronic exposures to chemicals in the environment. A passive sampler that was designed for occupational exposures can be used as such a tool. Laboratory validation under as many conditions as possible needs to be accomplished so as to characterize the sampler with known parameters. This paper describes the methods and results of an investigation into the validity of using a passive monitor to sample VOCs for a three-week period. Two concentration levels, two relative humidities, and five VOCs were studied. Results indicate that the samplers work best under conditions of high concentration with low relative humidity and low concentration with high relative humidity. For the passive sampler, excluding chloroform, percent deviations from the predicted values varied between ?41 and +22 percent; while the values between the passive and the active samplers varied between ?27 and +24 percent. Benzene, heptane, and perchloroethylene were sampled with equal precision and accuracy.     

A Tracer Study of Headspace Ventilation in a Collector Sewer

ABSTRACT

A field-scale tracer test was conducted to evaluate in-situ ventilation rates in a major collector sewer. The sewer under study was ~11 km long and ranged from 0.61 to 2.1 m in diameter. For the purposes of the tracer testing, the collector was divided into four reaches, each of which was tested individually. The tracer test involved injecting a measured volume of CO gas into a manhole over a short time period. CO concentrations were then measured in the collector headspace at selected manholes along the length of the reach.

The technique employed successfully measured average headspace velocities over extended lengths of the collector. In a section that had a relatively stagnant headspace, ~1.1 km of sewer could be evaluated, with substantial tracer loss attributed to losses to manholes. In a section of the sewer with elevated headspace velocities, a section ~7.0 km long was successfully tested with one injection of tracer gas. The velocities observed in the collector varied substantially with time and location in the collector. The lowest velocities measured were in the upstream sections, with a minimum observed value of 3.8 m/min. The highest velocities were observed in the downstream sections, with a maximum value of 31.5 m/min. The presence of a substantial drop structure appeared to reduce the headspace velocity in the upstream reach. In general, there was an increasing trend in gas-phase flows with distance along the length of the collector. Flows at the discharge end of the collector were almost 2 orders of magnitude greater than those at the beginning.     

Issues Related to Solution Chemistry in Mercury Sampling Impingers

ABSTRACT

Analysis of Hg speciation in combustion flue gases is often accomplished in standardized sampling trains in which the sample is passed sequentially through a series of aqueous solutions to capture and separate oxidized Hg (Hg²⁺) and elemental Hg (Hg⁰). Such methods include the Ontario Hydro (OH) and the Alkaline Mercury Speciation (AMS) methods, which were investigated in the laboratory to determine whether the presence of Cl₂ and other common flue gas species can bias the partitioning of Hg⁰ to front impingers intended to isolate Hg²⁺ species. Using only a single impinger to represent the front three impingers for each method, it was found that as little as 1-ppm Cl₂ in a simulated flue gas mixture led to a bias of approximately 10-20% of Hg⁰ misreported as Hg²+ for both the OH and the AMS methods. Experiments using 100-ppm Cl₂ led to a similar bias in the OH method, but to a 30-60% bias in the AMS method. These false readings are shown to be due to liquid-phase chemistry in the impinger solutions, and not necessarily to the gas-phase reactions between Cl₂ and Hg as previously proposed. The pertinent solution chemistry causing the interference