Bioretention cells (BRCs) have shown potential for storm water quantity and quality control. However, the phosphorus (P) removal in BRC has been variable due to differences of soil properties in filter media. The objectives of this research were to identify and evaluate P accumulation in filter media and to quantify effluent P reduction in BRC. Each cell has a sand and fly ash media designed to remove phosphorous. Filter media were collected in 2014 across the cell surface and to a depth of 0.6 m to quantify the P accumulation. The mean total P (T-P) concentration increased over the seven years of operation, but the changes were not statistically significant. The average Mehlich-3 P (M3-P) and water-soluble P (WS-P) concentrations in the media profiles showed higher P accumulation in the top 0.15 m. The average M3-P and WS-P concentrations between 0.15 m to 0.30 m, and 0.30 m to 0.60 m were variable on all four BRCs media. The media with 5% fly ash significantly retained M3-P and WS-P over the top 0.15 m. Stormwater influent and effluent samples from three of the BRCs monitored over one year showed reductions in both P concentration (68% to 75%) and P mass (76% to 93%).

Abstract:Microbial pollution in stormwater is a concern in urban areas across the U.S. and is a leading cause of water-quality impairment in the United States. This issue may be addressed through the use of best management practices (BMPs) and target limits for pathogenic indicator species. Bioretention is a commonly used low impact development strategy that addresses this growing pollution problem at the source. Bioretention removal efficiencies have been well studied when considering nutrients and heavy metals, but field-scale treatment data are limited for microbial indicators. The primary objective of this study was to quantify microbial removal by installed bioretention cells with fly-ash amended soils. Three bioretention cells in Grove, Oklahoma were monitored over one and a half years and the removal microbial efficiency was quantified. Overall, removal rates for E. coli, enterococci, and coliphage were highly variable, with mean and standard deviations for removals for each site respectively: E. coli 87%, 35%, and 43%; enterococci 97%, 95%, and 80%; and coliphage 38%, 75%, and 32%. The site with negative removal efficiency appears to have some groundwater intrusion during storm events. Based on this relatively limited data set, these fly-ash amended bioretention cells performed 49% better than those with a sand-only filter media layer currently reported in the literature. Based on this initial field study, it appears that fly-ash amended bioretention cells may be a viable option for enhanced microbial removal from stormwater runoff.

In 2007, ten bioretention cells were constructed in Oklahoma as part of a full-scale technology project to demonstrate stormwater phosphorus reduction. The filter media used was amended with 5%, Class C fly ash by weight to increase phosphorus and heavy metal retention. In 2014, core samples were collected from four of the cells, and three were instrumented for continuous water monitoring for the following year. This paper will review the design, construction, computer modeling of phosphorus retention, and measured phosphorus removal after seven years of operation. Total phosphorus retained in the sampled cells showed reductions in effluent water concentrations of 68 to 75%, while total effluent mass reductions of 51 to 93% were achieved. Total phosphorus accumulation in the cells measured in cores ranged from 0.33 to 0.60 kg/year, which was somewhat greater than the annual calculated effluent reduction of 0.27 to 0.41 kg/year. While good, phosphorus retention was not as high as computer modeling predicted. Other research on the cells, including hydraulics, heavy metal adsorption, and microbial transport, is summarized. Experimental challenges with phosphorus extraction from samples are also discussed. All experience and results suggest that fly ash amendments are an effective option for phosphorus removal in bioretention cells.