RESUMO
Anthropogenic microparticles (of synthetic, semisynthetic, or modified natural compositions) are globally pervasive, yet little is known about their distribution and storage in the subsurface despite their potential threats to belowground environments. We therefore assessed their amounts and characteristics in water and sediment from a cave in the United States. During a flood, water and sediment samples were collected at 8 sites every ~25 m along the cave passageways. Both sample types were evaluated for anthropogenic microparticles, while water was assessed for geochemistry (e.g., inorganic species) and sediment was evaluated for particle sizes. Additional water samples were collected during low flow at the same sites for further geochemical analysis to determine water provenance. We found anthropogenic microparticles in all samples that were mainly fibers (91 %) and clear (59 %). Both suspected (identified visually) and confirmed (identified with Fourier transform infrared spectroscopy; FTIR) anthropogenic microparticle concentrations were positively correlated between the compartments (r ≥ 0.83, p ≤ 0.01), but quantities in sediment were ~100 times those in water. These findings indicate that sediment sequesters anthropogenic microparticle pollution in the cave. Microplastic concentrations were similar among all sediment samples, but only one water sample at the main entrance contained microplastics. Treated cellulosic microparticle abundances in both compartments generally increased along the cave stream's flowpath, which we suspect is due to both their flood and airborne deposition. Water geochemical and sediment particle size data collected at a branch indicated at least two distinct water sources to the cave. However, anthropogenic microparticle assemblages did not differ between these sites, implying minimal variation in sourcing across the recharge area. Our results reveal that anthropogenic microparticles intrude karst systems and are stored in sediment. Karstic sediment consequently represents a potential source of "legacy" pollution to the water resources and fragile habitats found in these globally distributed landscapes.
RESUMO
Untreated wastewater entering the environment through leaking infrastructure and sewer overflows threatens both human and aquatic health. Water managers therefore need low cost, in situ methods to detect sewage contamination in real time to promptly employ mitigation strategies. However, wastewater has traditionally been identified in waterbodies using chemical and microbial tracers and indicators that can be non-unique to wastewater and often require complex and expensive analyses. Optical brighteners (synthetic brightening compounds present in laundry detergents and paper products) are emerging as ideal tracers of wastewater because of their quick and inexpensive field detection using handheld fluorometers. To test the efficacy of optical brighteners as standalone, in situ wastewater tracers, field readings of their fluorescence were compared with traditional wastewater analytes (e.g., B, F-, microbial indicators) at multiple points in time and space for a suburban watershed (Fishpot Creek, Saint Louis, Missouri, United States). We also used chemical tracers in three mixing models of endmembers to assess the wastewater fraction across the watershed. Compared to other analytes, optical brightener fluorescence measurements had the strongest correlation with wastewater infrastructure density (r = 0.71, p < 0.05), indicating their utility as tracers. All our endmember mixing models employing optical brightener readings predicted positive and significant correlations between the untreated wastewater fraction in streamflow and sewer pipe density at each site (r ≥ 0.77, p < 0.05). While using optical brightener readings for wastewater detection has some limitations (e.g., minor photodegradation), we found them to be more robust tracers than other analytes. Thus, optical brightener fluorescence measurements are an ideal initial screening tool for identifying wastewater contributions to the environment.
