Combining environmental, health, and safety features with a conductor like Screening Model for selecting green solvents for antibiotic analyses.

Extraction and chromatographic techniques for analyzing pharmaceutically active compounds necessitate large quantities of organic solvents, resulting in a high volume of hazardous waste. The concept of green solvents focuses on protecting the environment by reducing or even eliminating the use of toxic solvents. The main objective of this critical review article is to build a framework for choosing green solvents for antibiotic analyses. The article briefly discusses the chemical properties of ciprofloxacin, sulfamethoxazole, tetracycline, and trimethoprim, and the current state of methodologies for their analyses in water and wastewater. It evaluates the greenness of solvents used for antibiotic analyses and includes insights on the comparison between conventional and green solvents for the analyses. An economic and environmental health and safety analysis combined with a Conductor-like Screening Model for Real Solvent (COSMO-RS) molecular simulation technique for predicting extraction efficiency was used in the evaluation. Methyl acetate and propylene carbonate tied for the greenest solvents from an environmental and economic perspective, whereas the COSMO-RS approach suggests dimethyl sulfoxide (DMSO) as the most suitable candidate. Although DMSO ranked third environmentally and economically, after methyl acetate and propylene carbonate, it would be an ideal replacement of hazardous solvents if it could be manufactured at a lower cost. DMSO showed the highest extraction capacity, as it can interact with antibiotics through hydrophobic interaction and hydrogen bonding. This article can be used as a green solvent selection guide for developing sustainable processes for antibiotic analyses.

Hydraulic Fracturing Chemical Disclosure Policy and Data Analysis: Metrics and Trends in Transparency.

This research presents two new policy-level performance indicators for measuring hydraulic fracturing chemical transparency to address the limitations of existing metrics and provide additional perspectives to stakeholders. Existing indicators do not capture the change in proportions of hydraulic fracturing wells with publicly available chemical information or percent of ingredient mass withheld on chemical disclosure forms. Based on the new indicators, state-level policy changes and the FracFocus register have increased hydraulic fracturing chemical transparency over the past decade and continue to drive measurable improvements. The percent of wells with publicly disclosed ingredients increased from ∼0 to 95% (2010-2019), and the average percent of hydraulic fracturing fluid mass withheld on chemical disclosure forms decreased ∼46.8% (2013-2019). The percent ingredient mass withholding was used to compare the two current regulatory chemical disclosure form approaches (system and traditional). In 2019, the average percent of hydraulic fracturing fluid mass withheld on system approach chemical disclosure forms (0.044%) was 66.3% less than the traditional forms (0.132%). This research improves our capabilities to understand, evaluate, and communicate the effect of chemical transparency policy decisions and corporate practices. Recent lessons learnt from the oil and gas industry should be used to study broader chemical transparency policies, information systems, and communication strategies.

Photolytic fate of (E)- and (Z)-endoxifen in water and treated wastewater exposed to sunlight.

Endoxifen is the main active metabolite of a common cytostatic drug, tamoxifen. Endoxifen has been recently detected in the final effluent of municipal wastewater treatment plants. The antiestrogenic activity of endoxifen could bring negative effects to aquatic life if released to the water environment. This study elucidated the fate and susceptibility of (E)- and (Z)-endoxifen (2 µg mL-1, 1:1 wt ratio between the two easily interchangeable isomers) in wastewater and receiving surface water to sunlight. Phototransformation by-products (PBPs) and their toxicity were determined. Sunlight reduced at least 83% of endoxifen concentration in wastewater samples, whereas in surface water samples, 60% of endoxifen was photodegraded after 180 min of the irradiation. In ultrapure water samples spiked with endoxifen, PBPs were mainly generated via con-rotatory 6π-photocyclization, followed by oxidative aromatization. These PBPs underwent secondary reactions leading to a series of PBPs with different molecular weights. Eight PBPs were identified and the toxicity analysis via the Toxicity Estimation Software Tool revealed that seven of these PBPs are more toxic than endoxifen itself. This is likely due to the formation of poly-aromatic core in the PBPs due to exposure to sunlight. Therefore, highly toxic PBPs may be generated if endoxifen is present in water and wastewater exposed to sunlight. The presence, fates and activities of these PBPs in surface water especially at locations close to treated wastewater discharge points should be investigated.

Carbon-based adsorbents for fluoroquinolone removal from water and wastewater: A critical review.

This review summarizes the adsorptive removal of Fluoroquinolones (FQ) from water and wastewater. The influence of different physicochemical parameters on the adsorptive removal of FQ-based compounds is detailed. Further, the mechanisms involved in the adsorption of FQ-based antibiotics on various adsorbents are succinctly described. As the first of its kind, this paper emphasizes the performance of each adsorbent for FQ-type antibiotic removal based on partition coefficients of the adsorbents that is a more sensitive parameter than adsorption capacity for comparing the performances of adsorbents under various adsorbate concentrations and heterogeneous environmental conditions. It was found that π-π electron donor-acceptor interactions, electrostatic interactions, and pore-filling were the most prominent mechanisms for FQ adsorption by carbon and clay-based adsorbents. Among all the categories of adsorbents reviewed, graphene showed the highest performance for the removal of FQ antibiotics from water and wastewater. Based on the current state of knowledge, this review fills the gap through methodolically understanding the mechanism for further improvement of FQ antibiotics adsorption performance from water and wastewater.

Recent advances in photodegradation of antibiotic residues in water.

Antibiotics are widely present in the environment due to their extensive and long-term use in modern medicine. The presence and dispersal of these compounds in the environment lead to the dissemination of antibiotic residues, thereby seriously threatening human and ecosystem health. Thus, the effective management of antibiotic residues in water and the practical applications of the management methods are long-term matters of contention among academics. Particularly, photocatalysis has attracted extensive interest as it enables the treatment of antibiotic residues in an eco-friendly manner. Considerable progress has been achieved in the implementation of photocatalytic treatment of antibiotic residues in the past few years. Therefore, this review provides a comprehensive overview of the recent developments on this important topic. This review primarily focuses on the application of photocatalysis as a promising solution for the efficient decomposition of antibiotic residues in water. Particular emphasis was laid on improvement and modification strategies, such as augmented light harvesting, improved charge separation, and strengthened interface interaction, all of which enable the design of powerful photocatalysts to enhance the photocatalytic removal of antibiotics.

Effects of cathode coating materials and operational time on the mercury removal performance of electrokinetic remediation system for marine sediment.

Electrokinetic remediation (EK) is a promising in-situ technique for removing mercury (Hg) from contaminated sites; yet it demands long operational periods when conventional electrodes are used. Herein, we investigate the effectiveness of lab-prepared cathodes (Cu foam coated with reduced graphene oxide (rGO) or manganese oxide (MnO2)) to enhance Hg removal rates from sediment by EK. Although short term (2 h) Hg removal rates were insignificantly different (p-value > 0.05) when using the uncoated and coated Cu foam cathodes, long term (60 h) operations saw greater Hg removal by coated Cu foam cathodes over pure Cu foam, probably owing to the time required for Hg to migrate towards the electrodes from sediment. The highest Hg removal at the cathode was achieved when an αMnO2-coated Cu foam cathode was used with a strong-base anion exchange membrane (AEM) in the system. Using H3PO4, as a cathodic electrolyte resulted in a higher Hg removal efficiency than using NaCl and HCl electrolytes. Electromigration was found to be the dominant Hg-ions (e.g. HHgO2-, Hg2+) transport mechanism in the marine sediment during remediation. Overall, this research demonstrates that employing enhanced electrodes and AEMs can enhance Hg removal by EK processes in relatively shorter operating times than conventional EK processes.

Vacuum ultraviolet irradiation for mitigating dissolved organic nitrogen and formation of haloacetonitriles.

The main objective of this work was to investigate the feasibility of using vacuum ultraviolet (VUV, 185 + 254 nm) and ultraviolet (UV, 254 nm) for the reduction of dissolved organic nitrogen (DON) and haloacetonitrile formation potential (HANFP) of surface water and treated effluent wastewater samples. The results showed that the reduction of dissolved organic carbon (DOC), DON, hydrophobicity (HPO), absorbance at 254 nm (UV254), and fluorescence excitation-emission matrix (FEEM) of both water samples by VUV was higher compared to using UV. The addition of H2O2 remarkably improved the performances of VUV and UV. VUV/H2O2 exhibited the highest removal efficiency for DOC and DON. Even though HANFP increased at the early stage, its concentration decreased (19-72%) at the end of treatment (60 min). Decreases in DON (30-41%) and DOC (51-57%) led to HANFP reduction (53-72%). Moreover, FEEM revealed that substantial reduction in soluble microbial product-like compounds (nitrogen-rich organic) had a strong correlation with HANFP reduction, implying that this group of compounds act as a main precursor of HANs. The VUV/H2O2 system significantly reduced HANFP more than UV/H2O2 and therefore is suitable for controlling HAN precursors and HAN formation in drinking water and reclaimed wastewater.

Dissolved oxygen/free ammonia (DO/FA) ratio manipulation to gain distinct proportions of nitrogen species in effluent of entrapped-cell-based reactors.

Oxygen-limiting and/or free ammonia (FA)-accumulating conditions are two common operating strategies for partial nitrification in wastewater. Controlling either bulk dissolved oxygen (DO) or free ammonia (FA) concentration to maintain partial nitrification can be challenging due to the strong interdependency between these two parameters as substrates for ammonia oxidation. In this study, DO/FA ratio is proposed as a controlling parameter for partial nitrification by entrapped-cell-based reactors. At DO/FA >1.5, both ammonia and nitrite oxidation proceeded without inhibition leading to complete oxidation of ammonia to nitrate. An effluent containing nitrate as the main nitrogen species can be produced at these ratios. At a DO/FA ratio range of 0.2-1.5, ammonia oxidation proceeded without efficiency deterioration, while nitrite oxidation decreased with decreasing DO/FA ratio. At the ratios of 0.2-0.6, an effluent containing mainly nitrite can be generated. At DO/FA <0.2, both ammonia oxidation and nitrite oxidation were inhibited and the effluent with nearly equal molar of ammonia and nitrite was obtained. By controlling DO/FA ratio, effluents with different proportions of nitrogen species can be produced allowing the entrapped-cell-based system to be adaptable as an initial reactor for various nitrogen removal approaches.

Cryptosporidium infecting wild cricetid rodents from the subfamilies Arvicolinae and Neotominae.

We undertook a study on Cryptosporidium spp. in wild cricetid rodents. Fecal samples were collected from meadow voles (Microtus pennsylvanicus), southern red-backed voles (Myodes gapperi), woodland voles (Microtus pinetorum), muskrats (Ondatra zibethicus) and Peromyscus spp. mice in North America, and from bank voles (Myodes glareolus) and common voles (Microtus arvalis) in Europe. Isolates were characterized by sequence and phylogenetic analyses of the small subunit ribosomal RNA (SSU) and actin genes. Overall, 33·2% (362/1089) of cricetids tested positive for Cryptosporidium, with a greater prevalence in cricetids from North America (50·7%; 302/596) than Europe (12·1%; 60/493). Principal Coordinate analysis separated SSU sequences into three major groups (G1-G3), each represented by sequences from North American and European cricetids. A maximum likelihood tree of SSU sequences had low bootstrap support and showed G1 to be more heterogeneous than G2 or G3. Actin and concatenated actin-SSU trees, which were better resolved and had higher bootstrap support than the SSU phylogeny, showed that closely related cricetid hosts in Europe and North America are infected with closely related Cryptosporidium genotypes. Cricetids were not major reservoirs of human pathogenic Cryptosporidium spp.

Thermal remediation alters soil properties - a review.

Contaminated soils pose a risk to human and ecological health, and thermal remediation is an efficient and reliable way to reduce soil contaminant concentration in a range of situations. A primary benefit of thermal treatment is the speed at which remediation can occur, allowing the return of treated soils to a desired land use as quickly as possible. However, this treatment also alters many soil properties that affect the capacity of the soil to function. While extensive research addresses contaminant reduction, the range and magnitude of effects to soil properties have not been explored. Understanding the effects of thermal remediation on soil properties is vital to successful reclamation, as drastic effects may preclude certain post-treatment land uses. This review highlights thermal remediation studies that have quantified alterations to soil properties, and it supplements that information with laboratory heating studies to further elucidate the effects of thermal treatment of soil. Notably, both heating temperature and heating time affect i) soil organic matter; ii) soil texture and mineralogy; iii) soil pH; iv) plant available nutrients and heavy metals; v) soil biological communities; and iv) the ability of the soil to sustain vegetation. Broadly, increasing either temperature or time results in greater contaminant reduction efficiency, but it also causes more severe impacts to soil characteristics. Thus, project managers must balance the need for contaminant reduction with the deterioration of soil function for each specific remediation project.

Membrane Alterations in Pseudomonas putida F1 Exposed to Nanoscale Zerovalent Iron: Effects of Short-Term and Repetitive nZVI Exposure.

In this study, we report the effect of the commercial nanoscale zerovalent iron (nZVI) on environmental bacteria, emphasizing the importance of nZVI-bacterial membrane interaction on nZVI toxicity as well as the adaptability of bacteria to nZVI. Exposure of Pseudomonas putida F1 to 0.1, 1.0, and 5.0 g/L of nZVI caused the reduction in colony forming units (CFUs) substantially for almost 3 orders of magnitude. However, a rebound in the cell number was observed after the prolonged exposure except for 5.0 g/L nZVI at which bacterial viability was completely inhibited. Upon exposure, nZVI accumulated on and penetrated into the bacterial cell membrane. Cell membrane composition analysis revealed the conversion of the cis to trans isomer of unsaturated fatty acid upon short-term nZVI exposure, resulting in a more rigid membrane counteracting the membrane-fluidizing effect of nZVI. Several cycles of repetitive exposure of cells to 0.1 g/L nZVI induced a persistent phenotype of P. putida F1 as indicated by smaller colony morphology, a more rigid membrane, and higher tolerance to nZVI. A low interaction between nZVI particles and the surface of the nZVI-persistent phenotypic cells reduced the nZVI-induced membrane damage. This study unveils the significance of nZVI-membrane interaction on toxicity of nZVI toward bacteria.

Perceived risks of produced water management and naturally occurring radioactive material content in North Dakota.

Unconventional oil and gas development using hydraulic fracturing has caused conflict and controversy across the globe including the U.S. where some States banned the practice. Nevertheless, North Dakota (ND) has supported the practice because the State perceives the risks to be acceptable and because it has brought growth and opportunities to small communities. However, social acceptance of new technology is based on a number of factors and not contingent on economic benefits. To date, no research has been conducted to understand public risk perception of hazards associated with produced water from hydraulic fracturing in ND. This study focuses on understanding the risk perception of select ND stakeholder groups regarding produced water management and naturally occurring radioactive material. The software Qualtrics was used to create an online survey, collect data, and perform statistical analysis. The most important variables that seem to influence risk perception are the images and thoughts associated with produced water, level of knowledge about produced water handling and content, and knowing how to proceed in case of a spill of produced water. Overall, social risk perception could be in alignment with actual technical risk if availability of objective information is improved.

Nutrient balancing for phytoremediation enhancement of urea manufacturing raw wastewater.

Application of urea manufacturing wastewater to teak (Tectona grandis) trees, a fast growing tropical timber plants, is an environmentally-friendly and cost-effective alternative for treatment of nitrogen-rich wastewater. However, the plant growth is strongly limited by lack of phosphorus (P) and potassium (K) elements when the plants are irrigated with wastewater containing high concentration of nitrogen (N). A greenhouse experiment was conducted to optimize the efficiency of teak-based remediation systems in terms of nutrient balance. Twelve test solutions consisted of 4 levels of P (95, 190, 570, 1140 mgL-1) and 3 levels of K (95, 190, 570 mgL-1) with a constant level of N (190 mgL-1) were applied to teak seedlings every four days during the study period. Evapotranspiration rate, nutrient removal percentage, leaf surface area, dry weight and nutrient contents of experimental plants were determined and compared with those grown in control solution containing only N (N:P:K = 1:0:0). Teak seedlings grown in units with 1:0.5:1 N:P:K ratio were highly effective at nutrient removal upto 47%, 48% and 49% for N, P and K, respectively. Removal efficiency of teak plants grown in other experimental units decreased with increasing P and K concentrations in test solutions. The lowest nutrient removal and plant growth were recorded in units with 1:6:0.5 N:P:K ratio which received the highest ratio of P to K. The findings indicated that teak seedlings functioned effectively as phytoremediation plants for N-rich wastewater treatment when they were being supplied with proper concentrations of P and K.

Impact of operations and cleaning on membrane fouling at a wastewater reclamation facility.

Effects of operational changes on membrane fouling were evaluated for a wastewater reclamation facility. The focuses were on addition of a coagulant (ferric chloride) versus no addition and an accidental high chlorine (sodium hypochlorite) dose. Two membrane modules with different service ages, 3 years versus 9 months, were compared. Fouling rates ranged between 2 and 3 times higher during no ferric chloride addition. Chemical cleaning frequency was reduced by approximately 5 times during ferric chloride addition for older membranes, while it did not change for newer membranes. High chlorine dose had slightly improved membrane permeability for newer membrane, and reduced the transmembrane pressure (TMP) for both older and newer membranes. Chemical wash with enzymatic detergents substantially improved membrane permeability and reduced TMP for both older and newer membranes. Fouling index values indicated that coagulant addition had greater impact on performance recovery for older membranes than newer membranes. Successful and economical operation of membranes depends on fouling rate, which in this study was found to be a function of flux, membrane age, pretreatment, and cleaning type and frequency.

Cryptosporidium galli and novel Cryptosporidium avian genotype VI in North American red-winged blackbirds (Agelaius phoeniceus).

Proventriculus and intestinal samples from 70 North American red-winged blackbirds (Agelaius phoeniceus; order Passeriformes) were examined for the presence of Cryptosporidium by PCR amplification and sequence analysis of the 18S ribosomal RNA (18S rRNA), actin, and 70-kDa heat shock protein (HSP70) genes. Twelve birds (17.1 %) were positive for the Cryptosporidium 18S rRNA gene: six birds were positive at the proventriculus site only and six birds were positive at the proventriculus and intestinal sites. Sequence analysis of the 18S rRNA, actin and HSP70 genes showed the presence of the gastric species Cryptosporidium galli in a single proventriculus sample and a closely related genotype, which we have named Cryptosporidium avian genotype VI, in all other positive samples. These findings contribute to our understanding of Cryptosporidium diversification in passerines, the largest avian order.

Removal of aqueous cyanide with strongly basic ion-exchange resin.

The removal of cyanide (CN-) from aqueous solutions using a strongly basic ion-exchange resin, Purolite A-250, was investigated. The effects of contact time, initial CN- concentration, pH, temperature, resin dosage, agitation speed, and particle size distribution on the removal of CN- were examined. The adsorption equilibrium data fitted the Langmuir isotherm very well. The maximum CN- adsorption capacity of Purolite A-250 was found to be 44 mg CN- g(-1) resin. More than 90% CN- adsorption was achieved for most CN- solutions (50, 100, and 200 mg CN- L(-1)) with a resin dose of 2 g L(-1). The equilibrium time was ∼20 min, optimum pH was 10.0-10.5, and optimum agitation speed was 150 rpm. An increase in adsorption of CN- with increasing resin dosage was observed. Adsorption of CN- by the resin was marginally affected (maximum 4% variation) within an environmentally relevant temperature range of 20-50 °C. Fixed-bed column (20.5 mm internal diameters) experiments were performed to investigate the effects of resin bed depth and influent flow rate on breakthrough behaviour. Breakthrough occurred in 5 min for 0.60 cm bed depth while it was 340 min for 5.40 cm bed depth. Adsorption capacity was 25.5 mg CN- g(-1) for 5 mL min(-1) flow rate and 3.9 mg CN- g(-1) for 20 mL min(-1) flow rate. The research has established that the resin can be effectively used for CN- removal from aqueous solutions.

Selective adsorption of antibiotics from human urine using biochar modified by dimethyl sulfoxide, deep eutectic solvent, and ionic liquid.

Antibiotics present in human urine pose significant challenges for the use of urine-based fertilizers in agriculture. This study introduces a novel two-stage approach utilizing distinct biochar types to mitigate this concern. Initially, a modified biochar selectively adsorbed azithromycin (AZ), ciprofloxacin (CPX), sulfamethoxazole (SMX), trimethoprim (TMP), and tetracycline (TC) from human urine. Subsequently, a separate pristine biochar was employed to capture nutrients. Biochar, derived from sewage sludge and pyrolyzed at 550 and 700 °C, was modified using dimethyl sulfoxide, deep eutectic solvent, and ionic liquid to enhance antibiotic removal in the first stage. The modifications introduced hydrophilic functional groups (-OH/-COOH), which favor antibiotic adsorption. Adsorption kinetics followed the pseudo-second-order model, with the Langmuir isotherm model best describing the adsorption data. The maximum adsorption capacities for AZ, CPX, SMX, TMP, and TC after the modification were 196.08, 263.16, 81.30, 370.37, and 833.33 µg/g, respectively. Pristine biochar exhibited a superior ammonia adsorption capacity compared to the modified biochar. Hydrogen bonding, electrostatic attraction, and chemisorption drove antibiotic adsorption on the modified biochar. Regeneration efficiency declined due to solvent accumulation and potential byproduct formation on the biochar surface (<30% removal capacity after three cycles). This study presents innovative biochar modification strategies for selective antibiotic adsorption, laying the groundwork for environmentally friendly urine-based fertilizers in agriculture.

Upcycling waste polyethylene terephthalate (PET) bottles into high-performance activated carbon for electrochemical desalination.

Upcycling waste polyethylene terephthalate (PET) bottles has attracted intensive research interests. This simultaneously alleviates plastic pollution and achieves a waste-to-resource strategy. Waste PET water bottles were used to fabricate value-added activated carbon (AC) electrodes for capacitive deionization (CDI). The KOH activation temperature (greater than 700 °C) prominently affected the physi-chemical properties and desalination performance of PET-derived activated carbons (PET-AC). Profiting from a large Brunauer-Emmet-Teller specific surface area (1448 m2 g-1) with a good mesoporous structure (the ratio of the mesopore volume to the total pore volume was 41.3%), PET-AC-1000 (activated at 1000 °C) possessed a huge specific capacitance of 108 F g-1 for capacitive ion storage. Moreover, when utilized as the electrode material in single-pass CDI, PET-AC-1000 exhibited a maximum electrosorption capacity of 10.82 ± 0.11 mg g-1 and a low level of energy consumption (0.07 kWh mol-1), associated with good electrochemical charging-discharging cyclic stability. The results provide a promising facile approach to tackle the challenge of plastic pollution and promote the advancement of electrode materials for economic affordable and energy-efficient electrochemical desalination process, which meets the United Nations (UN) sustainable development goals (SDGs).

Leaching characteristics of nutrients in food waste digestate-derived biochar.

Food waste anaerobic digestion requires proper utilization of solid digestate, and pyrolysis emerges as an effective method to produce nutrient-rich biochar. This study investigated the leaching characteristics and speciation changes of nutrients in food waste digestate (FWD)-derived biochar pyrolyzed at 350 °C (BC350), 450 °C (BC450), and 550 °C (BC550). BC350 featured inorganic nitrogen, while BC450 and BC550 contained elevated organic nitrogen. Nitrogen, potassium, and dissolved organic carbon were released via a quick surface wash-off process. Polyphosphates prevailed in BC350 and leached through a fast diffusion-controlled process. BC450 and BC550 were dominated by Ca/Mg orthophosphates and released via a slow dissolution-controlled process. Leachates from BC450 and BC550 stimulated the shoot length of wheat seeds. After 5 leaching cycles, there were more aromatic dissolved organics, and BC450 and BC550 exhibited higher abundance of C-N and O-P-O. Overall, pyrolysis of FWD at 450 °C and 550 °C shows potential in producing slow-release biochar fertilizers for resource recycling.

Performance of wood waste biochar and food waste compost in a pilot-scale sustainable drainage system for stormwater treatment.

Sustainable drainage system (SuDS) for stormwater reclamation has the potential to alleviate the water scarcity and environmental pollution issues. Laboratory studies have demonstrated that the capacity of SuDS to treat stormwater can be improved by integrating biochar and compost in the filter media, whereas their performance in scaled-up applications is less reported. This study examines the effectiveness of a pilot-scale SuDS, bioswale followed by bioretention, amended with wood waste biochar (1, 2, and 4 wt.%) and food waste compost (2 and 4 wt.%) to simultaneously remove multiple pollutants including nutrients, heavy metals, and trace organics from the simulated stormwater. Our results confirmed that SuDS modified with both biochar (2 wt.%) and compost (2 wt.%) displayed superior water quality improvement. The system exhibited high removal efficiency (> 70%) for total phosphorus and major metal species including Ni, Pb, Cd, Cr, Cu, and Zn. Total suspended solids concentration was approaching the detection limit in the effluent, thereby confirming its capability to reduce turbidity and particle-associated pollutants from stormwater. Co-application of biochar and compost also moderately immobilized trace organic contaminants such as 2,4-dichlorophenoxyacetic acid, diuron, and atrazine at field-relevant concentrations. Moreover, the soil amendments amplified the activities of enzymes including ß-D-cellobiosidase and urease, suggesting that the improved soil conditions and health of microbial communities could possibly increase phyto and bioremediation of contaminants accumulated in the filter media. Overall, our pilot-scale demonstration confirmed that the co-application of biochar and compost in SuDS can provide a variety of benefits for soil/plant health and water quality.