Benin’s waterways are affected by several forms of pollution that are linked in particular to anthropic activities. This study aims to detect the presence of antibiotic residues, the frequency of antibiotic resistant bacteria and the levels of heavy metals in Benin’s waterways. 160 surface water samples from streams in Benin were collected. They were filtered by the membrane filtration method, then incubated on different media. The isolated bacterial species were identified by API 20E gallery and specific biochemical tests. After detection of the resistance profile of the latter, the antibiotic residues were quantified in the samples by the ELISA technique on plate and the physicochemical analyses were performed by Multi 3630 IDS SET KS2 multimeter. Finally, heavy metal levels were detected by the MERCK test kit method specific to each metal. The bacterial species mostly identified were Klebsiella pneumoniae (56.59%), Klebsiella spp. (18.68%), Enterobacter spp. (12.63%). The most abundant resistance of bacterial strains was to amoxicillin + clavulanic acid (92%), followed by metronidazole (86%). Metronidazole was the antibiotic with the highest residue concentration in the samples (6.578 to 6.829 µg/L), followed by ciprofloxacin (2.142 to 9.299 µg/L). Benin streams contain heavy metals such as mercury (0.454±0.129 µg/L), lead (0.040±0.50 mg/L), zinc (6.120±16.017 mg/L), nickel (0.155±0.233 mg/L) and cadmium (0.154±0.132 mg/L). The analysis of the physico-chemical parameters showed that, apart from electrical conductivity, all parameters comply with Beninese and World Health Organization standards. Actions must be taken to clean up these rivers to preserve the integrity of aquatic ecosystems in Benin.

The presence of microplastics (MPs) in freshwater systems that receive discharge of urban effluent implies a great environmental impact. In order to be able to generate proposals that solve this problem, it is necessary to know in detail the contributions of different MPs sources. The aim of this work was to study the contribution of urban sewage discharge to MPs pollution in a stream that runs through a medium-sized city. The spatial distribution of MPs with sizes between 100 μm and 1.5 mm present in surface water was measured and their characteristics, dimensions, shapes and identification were determined. Physical-chemical parameters of the stream water were measured, and a decrease in water quality was found due to wastewater treatment plants. The main source of MPs was effluent from the plants (97% of the total MPs), while the rest came from storm drains and discharge of tributaries. The maximum concentration of MPs found was around 72,000 MP/L (equivalent to 53 million MPs/s), at a point after discharge from both plants. Around 70% of MPs correspond to microfibers with a mean length of around 300 μm and a mean width of around 15 μm, and they are mainly polyethylene fibers. The remaining 30% of MPs are particles with lengths of around 140 μm. The transport of MPs between a point located after discharge of the plants and another point located about 3 km further on was studied, and no significant variation was found in the concentration of MPs. Electrical conductivity was used as a conservative tracer of MPs concentration. This work presents for the first time a detailed analysis of different contributions of MPs to a freshwater system in South America, which receives discharge of wastewater treatment plants, evidencing its important role in pollution.

In 2018, over 30,000 L of fluorine-free firefighting foam was used to extinguish an industrial warehouse fire of uncharacterized chemical and industrial waste. Contaminated firewater and runoff were discharged to an adjacent freshwater creek in Melbourne, Australia. In this study, we applied nontarget analysis using liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QToF-MS) to 15 surface water samples to investigate the presence of legacy, novel and emerging per-and polyfluoroalkyl substances (PFAS). We identified six novel and emerging fluorotelomer-based fluorosurfactants in the Australian environment for the first time, including: fluorotelomer sulfonamido betaines (FTABs or FTSA-PrB), fluorotelomer thioether amido sulfonic acids (FTSASs), and fluorotelomer sulfonyl amido sulfonic acids (FTSAS-So). Legacy PFAS including C₆–C₈ perfluoroalkyl sulfonic acids, C₄–C₁₀ perfluoroalkyl carboxylic acids, and perfluoro-4-ethylcyclohexanesulfonate were also detected in surface water. Of note, we report the first environmental detection of ethyl 2-ethenyl-2-fluoro-1-(trifluoromethyl) cyclopropane-1-carboxylate. Analysis of several Class B certified fluorine-free foam formulations allowed for use in Australia revealed that there was no detectable PFAS. Patterns in the homologue profiles of fluorotelomers detected in surface water are consistent with environments impacted by fluorinated aqueous film-forming foams. These results provide strong evidence that firewater runoff of stockpiled fluorinated firefighting foam was the dominant source of detectable PFAS to the surrounding environment.

Forest management can alter the mobilization of mercury (Hg) into headwater streams and its conversion to methylmercury (MeHg), the form that bioaccumulates in aquatic biota and biomagnifies through food webs. As headwater streams are important sources of organic materials and nutrients to larger systems, this connectivity may also increase MeHg in downstream biota through direct or indirect effects of forestry on water quality or food web structure. In this study, we collected water, seston, food sources (biofilm, leaves, organic matter), five macroinvertebrate taxa and fish (slimy sculpin; Cottus cognata) at 6 sites representing different stream orders (1–5) within three river basins with different total disturbances from forestry (both harvesting and silviculture). Methylmercury levels were highest in water and some food sources from the basin with moderate disturbance (greater clearcutting but less silviculture). Water, leaves, stoneflies and fish increased in MeHg or total Hg along the river continuum in the least disturbed basin, and there were some dissipative effects of forest management on these spatial patterns. Trophic level (δ¹⁵N) was a significant predictor of MeHg (and total Hg in fish) within food webs across all 18 sites, and biomagnification slopes were significantly lower in the basin with moderate total disturbance but not different in the other two basins. The elevated MeHg in lower trophic levels but its reduced trophic transfer in the basin with moderate disturbance was likely due to greater inputs of sediments and of dissolved organic carbon that is more humic, as these factors are known to both increase transport of Hg to streams and its uptake in primary producers but to also decrease MeHg bioaccumulation in consumers. Overall, these results suggest that the type of disturbance from forestry affects MeHg bioaccumulation and trophic transfer in stream food webs and some longitudinal patterns along a river continuum.

To reduce direct discharges of surface runoff to receiving waters, separate sewer systems have been implemented, with runoff retention basins (RRB) for pollutant pretreatment by sedimentation and infiltration. However, due to frequent and intense precipitation events, most RRBs are overwhelmed by runoff resulting in overflow into the receiving freshwater bodies. Hence, the present study evaluates the impact of traffic-related runoff overflow on metal concentrations in sediment and Gammarus sp. Downstream of the RRB outfall in the receiving stream. Samples were collected from the RRB, upstream (reference site) and at different distances downstream from the RRB outfall in the stream. The samples were analyzed for the presence and distribution of metals using ICP-MS. Furthermore, ecotoxicological effects of the overflow on benthic species were assessed using Lumbriculus variegatus exposed to the field sediments. Our findings reveal that overflow of the RRB results in elevated traffic-related metal concentrations in sediment and biota of the stream. Within the first 50 m downstream increased sediment metal concentrations were found. The gammarids downstream of the RRB outfall showed an increased accumulation of several metals. Similarly, the metals were found to be taken up by the endobenthic L. variegatus under laboratory conditions and the bioaccumulation pattern was related to the sediment concentrations. Bioaccumulation by both organisms is an indication that overflow of the RRB also leads to uptake of increased element amounts in organisms downstream. Laboratory-based studies addressing standard toxicity endpoints showed no clear toxic effects on growth and reproduction. However, elevated levels of metallothioneins were measured in the annelids during the test period. This indicates a physiological response induced by increased metal concentrations due to RRB overflow. Hence, the results of this study show that discharges by the RRB increase the metal concentration in the receiving stream with the possibility of adverse effects on organisms.

Wetlands can improve water quality, but they are also recognized as important sources of greenhouse gases (GHG) such as nitrous oxide (N₂O) and methane (CH₄). Emissions of these gases from wetland ecosystems, especially those in headwaters, are poorly understood. Here, we determined monthly concentrations of dissolved N₂O and CH₄ in a headwater stream of the Taihu Lake basin of China that contains both wetland and non-wetland reaches. Daily GHG dynamics in the wetland reach were also investigated. Riverine N₂O and CH₄ concentrations generally varied within 10–30 nmol L⁻¹ and 0.1–1.5 μmol L⁻¹, respectively. CH₄ saturation levels in the wetland reach were about seven times higher than those in the non-wetland reach, but there was no difference in N₂O saturation. In the wetland reach, saturation levels of CH₄ peaked in July, coincident with a dip in N₂O saturation to levels below its saturated solubility. This underscores that hotspots of CH₄ production and sinks for N₂O can occur occasionally in wetlands in mid-summer, when vegetative growth and microbial activities are high. Diurnal measurements indicated that CH₄ saturation in water flows passing through the wetlands from midnight through the early morning can surge to levels 10 times higher than those detected at other times of the day. Simultaneously, saturation levels of N₂O decreased by 75%, indicating a net consumption of N₂O. Changes in nutrient supply determined by upstream inflows, as well as dissolved oxygen, pH, and other environmental factors mediated by the wetlands, correlate with the differentiated behavior of N₂O and CH₄ production in wetlands. Additional work will be necessary to confirm the roles of these factors in regulating GHG emissions in riverine wetlands.

Use of elemental mercury (Hg⁰) to enhance placer gold recovery is an effective method dating back centuries, but is associated with significant atmospheric Hg⁰ losses. This method was widely used in the Canadian Klondike region during most of the 20th century when the mining industry experienced rapid growth. While the health risks associated with Hg⁰ pollution are now well understood, few studies have assessed the environmental legacy of Hg⁰ use in the Klondike. We used an annually resolved Picea glauca tree-ring Hg record (1864–2015) to reconstruct and evaluate changes in local atmospheric Hg⁰ concentrations associated with gold production at the Bear Creek mining camp. Major temporal trends in the record are consistent with the scale of Bear Creek operations and are distinct from background trends at an unimpacted control site. Tree-ring Hg concentration increased most rapidly from 1923 to 1930, a period when several major mining operations were consolidated at Bear Creek. The highest Hg concentrations, ∼2.5× greater than pre-mining era, occurred in the 1930s, coinciding with maximum gold production at this site. Post-World War II economic factors adversely affected the industry, causing declining tree-ring Hg concentrations from 1939 to 1966. Closure of the Bear Creek camp in 1966 coincided with the strongest tree-ring Hg decline, although a return to background levels did not occur until the 1990s, likely due to re-emission of legacy Hg⁰ from contaminated soils. Finally, a robust increase was observed over the last decade, similar to other tree-ring Hg records in N.W. Canada, which is linked to rising Hg⁰ emissions in Asia. The Bear Creek tree-ring Hg record provides a unique opportunity to study the impact of Klondike gold mining on the local environment at annual resolution and demonstrates great potential to use Picea tree rings to study past changes in atmospheric Hg⁰ from local and global emissions.A 151-year long, annually resolved tree-ring Hg record was developed at a historic Klondike gold-mining site to investigate the influence of mining-related Hg⁰ emissions on the local atmosphere and environment. Compared to a control site, the tree-ring Hg record documents highly elevated atmospheric Hg⁰ concentrations during the period mining activities were ongoing at this site.

With increasing population growth and climate change, de facto reuse practices are predicted to increase globally. We investigated a longitudinal gradient within the Uhlava River, a representative watershed, where de facto reuse is actively occurring, during Fall and Spring seasons when instream flows vary. We observed human pharmaceutical levels in the river to continuously increase from the mountainous areas upstream to downstream locations and a potable intake location, with the highest concentrations found in small tributaries. Significant relationship was identified between mass flow of pharmaceuticals and the size of human populations contributing to wastewater treatment plant discharges. Advanced ozonation and granular activated carbon filtration effectively removed pharmaceuticals from potable source waters. We observed a higher probability of encountering a number of targeted pharmaceuticals during colder Spring months when stream flows were elevated compared to warmer conditions with lower flows in the Fall despite a dilution paradigm routinely applied for surface water quality assessment and management efforts. Such observations translated to greater water quality hazards during these higher Spring flows. Future water monitoring efforts should account for periods when higher chemical uses occur, particularly in the face of climate change for regions experiencing population growth and de facto reuse.

Aquatic hyphomycetes (AHs), a group of saprotrophic fungi adapted to submerged leaf litter, play key functional roles in stream ecosystems as decomposers and food source for higher trophic levels. Fungicides, controlling fungal pathogens, target evolutionary conserved molecular processes in fungi and contaminate streams via their use in agricultural and urban landscapes. Thus fungicides pose a risk to AHs and the functions they provide. To investigate the impacts of fungicide exposure on the composition and functioning of AH communities, we exposed four AH species in monocultures and mixed cultures to increasing fungicide concentrations (0, 5, 50, 500, and 2500 μg/L). We assessed the biomass of each species via quantitative real-time PCR. Moreover, leaf decomposition was investigated. In monocultures, none of the species was affected at environmentally relevant fungicide levels (5 and 50 μg/L). The two most tolerant species were able to colonize and decompose leaves even at very high fungicide levels (≥500 μg/L), although less efficiently. In mixed cultures, changes in leaf decomposition reflected the response pattern of the species most tolerant in monocultures. Accordingly, the decomposition process may be safeguarded by tolerant species in combination with functional redundancy. In all fungicide treatments, however, sensitive species were displaced and interactions between fungi changed from complementarity to competition. As AH community composition determines leaves’ nutritional quality for consumers, the data suggest that fungicide exposures rather induce bottom-up effects in food webs than impairments in leaf decomposition.

An industrial warehouse illegally storing a large quantity of unknown chemical and industrial waste ignited in an urban area in Melbourne, Australia. The multiday fire required firefighters to use large amounts of fluorine-free foam that carried contaminated firewater runoff into an adjacent freshwater creek. In this study, the occurrence and fate of 42 per- and polyfluoroalkyl substances (PFASs) was determined from triplicate surface water samples (n = 45) from five locations (upstream, point-source, downstream; 8 km) over three sampling campaigns from 2018 to 2020. Out of the 42 target PFASs, perfluorocarboxylates (PFCAs: C4–C14), perfluoroalkane sulfonates (PFSAs: C4–C10), and perfluoroalkyl acid precursors (e.g. 6:2 fluorotelomer sulfonate (6:2 FTSA)) were ubiquitously detected in surface waters (concentration ranges: <0.7–3000 ng/L). A significant difference in ΣPFAS concentration was observed at the point-source (mean 5500 ng/L; 95% CI: 4800, 6300) relative to upstream sites (mean 100 ng/L; 95% CI: 90, 110; p ≤ 0.001). The point-source ΣPFAS concentration decreased from 5500 ± 1200 ng/L to 960 ± 42 ng/L (−83%) after two months and to 430 ± 15 ng/L (−98%) two years later. 6:2 FTSA and perfluorooctanesulfonate (PFOS) dominated in surface water, representing on average 31% and 20% of the ΣPFAS, respectively. Emerging PFASs including a cyclic perfluoroalkanesulfonate (PFECHS) and a C4 perfluoroalkane sulfonamide (FBSA) were repeatedly present in surface water (concentration ranges <0.3–77 ng/L). According to the updated Australian PFAS guidelines for ecological conservation, the water samples collected at the time of monitoring may have posed a short-term risk to aquatic organisms in regard to PFOS levels. These results illustrate that acute high dose exposure to PFASs can result from industrial fires at sites storing or stockpiling PFAS-based waste products. Continued monitoring will be crucial to evaluate potential long-term risk to wildlife in the region.