Nationwide Mass Inventory and Degradation Assessment of Plastic Contact Lenses in US Wastewater.

Plastics pose ecological and human health risks, with disposable contact lenses constituting a potential high-volume pollution source. Using sales data and an online survey of lens users (n = 416) alongside laboratory and field experiments at a conventional sewage treatment plant, we determined the environmental fate and mass inventories of contact lenses in the United States. The survey results revealed that 21 ± 0.8% of lens users flush their used lenses down the drain, a loading equivalent to 44 000 ± 1700 kg y-1 of lens dry mass discharged into US wastewater. Biological treatment of wastewater did not result in a measurable loss of plastic mass (p = 0.001) and caused only very limited changes in the polymer structure, as determined by µ-Raman spectroscopy. During sewage treatment, the lenses were found to accumulate as fragments in sewage sludge, resulting in an estimated accumulation of 24 000 ± 940 kg y-1 of microplastics destined for application on US agricultural soils contained in sewage sludge. Recycling of the contact lenses and their packaging amounted to only 0.04% of the total waste volume associated with contact lens use. This is the first study to identify contact lenses and more specifically silicone hydrogels, as a previously overlooked source of plastic and microplastic pollution.

Occurrence and tissue-specific partitioning of alternative brominated flame retardants in northwest Atlantic harbor seal pups (Phoca vitulina vitulina).

Brominated flame retardants such as polybrominated diphenyl ethers (PBDEs) have been used for decades until evidence of negative health effects led to bans in many countries. PBDEs have since been replaced by alternative legacy compounds or newly developed chemicals. In this study, eight alternative brominated flame retardants were analyzed in blubber and liver of harbor seal pups (≤6 months) from the Northwest Atlantic collected during 2001-2010 to elucidate concentrations, patterns, contamination trends, potential maternal transfer, and tissue partitioning. All compounds were detected in liver and blubber tissues with hexabromocyclododecane (HBCD) isomers and 2-ethylhexyl 2,3,4,5-tetrabromobenzoate (TBB) predominating. Overall, α-HBCD was the dominant HBCD isomer in both tissues although the concentrations of γ-HBCD exceeded those of α-HBCD in seven pups, indicating their mothers may have had alternative dietary patterns or recent exposure to the commercial mixture. Although it was detected in less than half of the samples, to our knowledge, this is the first study to report tetrabromobisphenol A (TBBPA) concentrations in multiple tissues of a top marine predator. For the brominated components of Firemaster® flame retardants, TBB concentrations exceeded bis-(2-ethylhexyl)-tetrabromophthalate (TBPH). This pattern may result from recent exposure to commercial mixtures in which TBB exceeds TBPH 4:1 or from differences in perinatal or lactational transfer efficiency of the two compounds. Between the two tissues, lipid-normalized ß-HBCD, γ-HBCD, TBB and decabromodiphenyl ethane (DBDPE) concentrations were significantly higher in liver than blubber. This indicates that the bioaccumulation of these chemicals is not simply related to lipid dynamics but may be linked to blood proteins. This study demonstrates that harbor seal pups from this region are contaminated with alternative flame retardants passed to them via placental or lactational transfer. Given the evidence for negative health effects of these chemicals, this contamination adds additional pressure on the first year survival of these young, developing animals.

Alternative and legacy flame retardants in marine mammals from three northern ocean regions.

Flame retardants are globally distributed contaminants that have been linked to negative health effects in humans and wildlife. As top predators, marine mammals bioaccumulate flame retardants and other contaminants in their tissues which is one of many human-imposed factors threatening population health. While some flame retardants, such as the polybrominated diphenyl ethers (PBDE), have been banned because of known toxicity and environmental persistence, limited data exist on the presence and distribution of current-use alternative flame retardants in marine mammals from many industrialized and remote regions of the world. Therefore, this study measured 44 legacy and alternative flame retardants in nine marine mammal species from three ocean regions: the Northwest Atlantic, the Arctic, and the Baltic allowing for regional, species, age, body condition, temporal, and tissue comparisons to help understand global patterns. PBDE concentrations were 100-1000 times higher than the alternative brominated flame retardants (altBFRs) and Dechloranes. 2,2',4,5,5'-pentabromobiphenyl (BB-101) and hexabromobenzene (HBBZ) were the predominant altBFRs, while Dechlorane-602 was the predominant Dechlorane. This manuscript also reports only the second detection of hexachlorocyclopentadienyl-dibromocyclooctane (HCDBCO) in marine mammals. The NW Atlantic had the highest PBDE concentrations followed by the Baltic and Arctic which reflects greater historical use of PBDEs in North America compared to Europe and greater industrialization of North America and Baltic countries compared to the Arctic. Regional patterns for other compounds were more complicated, and there were significant interactions among species, regions, body condition and age class. Lipid-normalized PBDE concentrations in harbor seal liver and blubber were similar, but HBBZ and many Dechloranes had higher concentrations in liver, indicating factors other than lipid dynamics affect the distribution of these compounds. The health implications of contamination by this mixture of compounds are of concern and require further research.

Degradation of Polyvinyl Alcohol in US Wastewater Treatment Plants and Subsequent Nationwide Emission Estimate.

Polyvinyl alcohol (PVA) is a water-soluble plastic commercially used in laundry and dish detergent pods (LDPs) for which a complete understanding of its fate in the environment and subsequent consequences is lacking. The objective of this study was to estimate the US nationwide emissions of PVA resulting from domestic use of LDPs, corroborated by a nationwide, online consumer survey and a literature review of its fate within conventional wastewater treatment plants (WWTPs). Peer-reviewed publications focusing on the degradation of PVA in critical processes of WWTPs were shortlisted as a part of the literature review, and subsequent degradation data was extracted and applied to a model with a set of assumptions. Survey and model results estimated that approximately 17,200 ± 5000 metric ton units per year (mtu/yr) of PVA are used from LDPs in the US, with 10,500 ± 3000 mtu/yr reaching WWTPs. Literature review data, when incorporated into our model, resulted in ~61% of PVA ending up in the environment via the sludge route and ~15.7% via the aqueous phase. PVA presence in the environment, regardless of its matrix, is a threat to the ecosystem due to the potential mobilization of heavy metals and other hydrophilic contaminants.

Author Correction: The vertical distribution and biological transport of marine microplastics across the epipelagic and mesopelagic water column.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Chemical and physical changes of microplastics during sterilization by chlorination.

Wastewater treatment plants are known to release microplastics that have been detected in aquatic and terrestrial organisms constituting part of the human diet. Chlorination of wastewater-borne microplastics was hypothesized to induce chemical and physical changes detectable by Raman spectroscopy and differential scanning calorimetry (DSC). In the laboratory, virgin plastics (∼0.05 × 2 × 2 mm) were exposed to differing sterilization conditions representative of dosages used in the disinfection of drinking water, wastewater, and heavily contaminated surfaces. Polypropylene (PP) was most resistant to chlorination, followed by high density polyethylene (HDPE) and polystyrene (PS). Polystyrene showed degradation, indicated by changes in Raman peak widths, at concentration-time regimes (CT values) as low as 75 mg min/L, whereas HDPE and PP remained unaltered even at chlorine doses characteristic of wastewater disinfection (150 mg min/L). However, HDPE and PS were not completely resistant to oxidative attack by chlorination. Under extremely harsh conditions, shifts in Raman peaks and the formation of new bonds were observed. These results show that plastics commonly used in consumer products can be chemically altered, some even under conditions prevailing during wastewater treatment. Changes in polymer properties, observed for HDPE and PP under extreme exposure conditions only, are predicted to alter the risk microplastics pose to aquatic and terrestrial biota, since an increase in carbon-chlorine (C-Cl) bonds is known to increase toxicity, rendering the polymers more hydrophobic and thus more prone to adsorb, accumulate, and transport harmful persistent pollutants to biota in both aquatic and terrestrial environments.

The vertical distribution and biological transport of marine microplastics across the epipelagic and mesopelagic water column.

Plastic waste has been documented in nearly all types of marine environments and has been found in species spanning all levels of marine food webs. Within these marine environments, deep pelagic waters encompass the largest ecosystems on Earth. We lack a comprehensive understanding of the concentrations, cycling, and fate of plastic waste in sub-surface waters, constraining our ability to implement effective, large-scale policy and conservation strategies. We used remotely operated vehicles and engineered purpose-built samplers to collect and examine the distribution of microplastics in the Monterey Bay pelagic ecosystem at water column depths ranging from 5 to 1000 m. Laser Raman spectroscopy was used to identify microplastic particles collected from throughout the deep pelagic water column, with the highest concentrations present at depths between 200 and 600 m. Examination of two abundant particle feeders in this ecosystem, pelagic red crabs (Pleuroncodes planipes) and giant larvaceans (Bathochordaeus stygius), showed that microplastic particles readily flow from the environment into coupled water column and seafloor food webs. Our findings suggest that one of the largest and currently underappreciated reservoirs of marine microplastics may be contained within the water column and animal communities of the deep sea.