A Method for Spatially Explicit Representation of Sub-watershed Sediment Yield,Southern California,USA

We present here a method to integrate geologic, topographic, and land-cover data in a geographic information system to provide a fine-scale, spatially explicit prediction of sediment yield to support management applications. The method is fundamentally qualitative but can be quantified using preexisting sediment-yield data, where available, to verify predictions using other independent data sets. In the 674-km² Sespe Creek watershed of southern California, 30 unique “geomorphic landscape units” (GLUs, defined by relatively homogenous areas of geology, hillslope gradient, and land cover) provide a framework for discriminating relative rates of sediment yield across this landscape. Field observations define three broad groupings of GLUs that are well-associated with types, relative magnitudes, and rates of erosion processes. These relative rates were then quantified using sediment-removal data from nearby debris basins, which allow relatively low-precision but robust calculations of both local and whole-watershed sediment yields, based on the key assumption that minimal sediment storage throughout most of the watershed supports near-equivalency of long-term rates of hillslope sediment production and watershed sediment yield. The accuracy of these calculations can be independently assessed using geologically inferred uplift rates and integrated suspended sediment measurements from mainstem Sespe Creek, which indicate watershed-averaged erosion rates between about 0.6–1.0 mm year^?1 and corresponding sediment yields of about 2 × 10³ t km^?2 year^?1. A spatially explicit representation of sediment production is particularly useful in a region where wildfires, rapid urban development, and the downstream delivery of upstream sediment loads are critical drivers of both geomorphic processes and land-use management.     

Estimation of terrestrial chemical spill risk factors using a modified Delphi approach

The large number of chemical spills each year in the United States presents a potentially significant risk to human health and the environment. In an effort to manage this risk, the authors are developing a screening tool to assess the immediate threat to human and environmental receptors from land-based chemical spills. As part of this development effort, a modified Delphi survey was employed to determine the most important factors governing this risk and the relative importance of these factors. Results of the survey indicate that accounting for the attributes of the spilled chemical as well as the characteristics of the surrounding environment is imperative in making informed decisions regarding spill planning and mitigation. Survey results further indicate the greatest concern during spill events to be the risk to human health, which must be considered directly as well as factored into decisions concerning the protection of environmental receptors.     

Water-based condensation particle counters for environmental monitoring of ultrafine particles

TSI Inc. (Shoreview, MN) has introduced three new water-based condensation particle counters (WCPCS) that were designed to detect airborne particles larger than 2.5 nm (model 3786), 5 nm (model 3785), and either 10 or 20 nm (model 3782). These WCPCs are well suited for real-time, environmental monitoring of number concentration of airborne ultrafine particles. Their unique design incorporates the use of water as the working fluid instead of alcohol. Water is odor free, readily available, and eliminates the problem of water condensation and absorption into alcohol working fluids during operation in humid environments. In this study, the performance of three TSI WCPCs was characterized for several aerosol compositions, including sucrose, salt (NaCl), dioctyl sebacate (DOS), dioctyl phthalate (DOP), emery oil (poly-alpha-olefin), silver, impurity residue particles, and ambient aerosol particles. All particles were size selected using a nano differential mobility analyzer (nano-DMA; model 3085, TSI Inc.) to create monodisperse challenge aerosols. The challenge aerosol was mixed uniformly with clean makeup flow and split into a WCPC and a reference instrument to determine the counting efficiency of the WCPC. For the model 3785 WCPC, the D50 (i.e., the particle diameter with 50% counting efficiency) was determined to be 3.1 nm for salt particles, 4.7 nm for sucrose and ambient particles, 5.6 nm for silver particles, and >50 nm for ultrapure oil particles. The sensitivity to oil droplets increased dramatically (D50 < 10 nm) when the oil was slightly contaminated. The D50 of model 3786 ultrafine water-based CPC (UWCPC) was 2.4 nm for impurity residue particles. The D50 of the model 3782 WCPC was 10.8 (with a nominal setting of 10 nm) or 19.8 nm (with a nominal setting of 20 nm) for sucrose particles. All three WCPCs have response times of less than 2 or 3 sec and are therefore able to detect fast-changing events.     

The Role of Mineral Weathering Rate Determinations in Generating Uncertainties in the Calculation of Critical Loads of Acidity and their Exceedance

Current legislation within Europe aimed at limitingecosystem damage resulting from inputs of atmosphericpollution is based on the critical load concept. Mineralweathering rates are central to the calculation ofcritical loads (acceptable levels) of acid deposition.The authors have undertaken a number of studies whichillustrate the complications and limitations inherent inpredicting mineral weathering rates and the implicationswhich these have for critical loads calculations andmapping. Calculated weathering rates and critical loadsfor two acid-sensitive parent materials (greywackes andgranites) are presented and are used to illustrate theimpact that uncertainty can have on critical loadexceedances. The results have obvious implications forportraying the uncertainties of critical loads to policy makers.     

Polychlorinated biphenyls and polybrominated diphenyl ethers in the North American atmosphere

To assess the spatial concentration variability of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in the atmosphere on a large continental scale, their annually integrated air concentrations were determined in 2000/2001 using XAD-based passive air samplers (PAS). The network included 40 stations in Canada, the United States, Mexico, Belize and Costa Rica, and covered 72 degrees of latitude and longitude. Total concentrations of PCB and PBDE congeners ranged from below the detection limit to 130 ng PAS-1 and 24 ng PAS-1, respectively. PCBs displayed a large variation between urban, rural and remote sites, whereas PBDEs did not follow such a pattern. Open burning of "Penta"-containing waste may have contributed to the PBDEs detected in the air samples from rural and remote areas. Air from the Canadian Arctic had a relatively higher percentage of lighter PCB congeners than air sampled in the tropical region, which is interpreted as evidence for global fractionation.