A Unique Monitoring Method for Fecal and Sewage-Derived Chemical Pollution Utilizing International Pellet Watch Approach.

This study established a unique approach to assess fecal contamination by measuring fecal sterols, especially coprostanol (5ß-cholestanol-3ß-ol, 5ß) and cholestanol (5α-cholestan-3ß-ol, 5α) and their ratio 5ß/(5ß + 5α) alongside triclosan (TCS) and methyl-triclosan (MTC) in beached plastic pellets across 40 countries. Coprostanol concentrations ranged from 3.6 to 8190 ng/g pellet with extremely high levels in densely populated areas in African countries. The 5ß/(5ß + 5α) ratio was not affected by the difference in residence time of pellets in aquatic environments, and their spatial pattern showed a positive correlation with that of sedimentary sterols, demonstrating its reliability as an indicator of fecal contamination. Pellets from populated areas of economically developing countries, i.e., Africa and Asia, with lower coverage of wastewater treatment exhibited higher 5ß/(5ß + 5α) ratios (∼0.7) corresponding to ∼1% sewage in seawater, while pellets from developed countries, i.e., the USA, Canada, Japan, and Europe, with higher coverage of modern wastewater treatment displayed lower ratios (∼0.5), corresponding to the first contact limit. Triclosan levels were higher in developing countries (0.4-1298 ng/g pellet), whereas developed countries showed higher methyl-triclosan levels (0.5-70 ng/g pellet) due to TCS conversion during secondary treatment. However, some samples from Japan and Europe displayed higher TCS levels, suggesting contributions from combined sewage overflow (CSO). Combination of 5ß/(5ß + 5α) and MTC/TCS ratios revealed extreme fecal contamination from direct input of raw sewage due to inadequate treatment facilities in some African and South and Southeast Asian countries.

A dataset of organic pollutants identified and quantified in recycled polyethylene pellets.

Plastics are produced with a staggering array of chemical compounds, with many being known to possess hazardous properties, and others lacking comprehensive hazard data. Furthermore, non-intentionally added substances can contaminate plastics at various stages of their lifecycle, resulting in recycled materials containing an unknown number of chemical compounds at unknown concentrations. While some national and regional regulations exist for permissible concentrations of hazardous chemicals in specific plastic products, less than 1 % of plastics chemicals are subject to international regulation [1]. There are currently no policies mandating transparent reporting of chemicals throughout the plastics value chain or comprehensive monitoring of chemicals in recycled materials. The dataset presented here provides the chemical analysis of 28 samples of recycled High-Density Polyethylene (HDPE) pellets obtained from various regions of the Global South, along with a reference sample of virgin HDPE. The analysis comprises both Target and Non-Targeted Screening approaches, employing Liquid Chromatography-High-Resolution Mass Spectrometry (LC-HRMS) and Gas Chromatography-High-Resolution Mass Spectrometry (GC-HRMS). In total, 491 organic compounds were detected and quantified, with an additional 170 compounds tentatively annotated. These compounds span various classes, including pesticides, pharmaceuticals, industrial chemicals, plastic additives. The results highlight the prevalence of certain chemicals, such as N-ethyl-o-Toluesulfonamide, commonly used in HDPE processing, found in high concentrations. The paper provides a dataset advancing knowledge of the complex chemical composition associated with recycled plastics.

Total lead concentration in new decorative enamel paints in Lebanon, Paraguay and Russia.

Lead concentrations in new enamel decorative paints were determined in three countries in different areas of the world where data were not previously available. The average total lead concentration of the enamel decorative paints purchased in Lebanon, Paraguay and Russia was 24,500ppm (ppm, dry weight), more than 270 times the current limit of 90ppm in Canada and in the United States. Sixty-three percent of these paints contained concentrations greater than 90ppm. Fifty-nine percent contained concentrations greater than 600ppm, the current limit in some countries. The maximum concentrations found were 236,000ppm in Lebanon, 169,000ppm in Paraguay and 52,900ppm in Russia. An average of 29% of the samples contained exceedingly high lead concentrations, >=10,000ppm. Five brands of paint were sampled in each of Lebanon and Paraguay and seven in Russia. Three colors from each brand were analyzed. For five of the six samples of the two brands in Lebanon with affiliations outside the country, the lead concentrations ranged from 1360ppm to 135,000ppm. In Lebanon the maximum concentration in the Egypt-affiliated brand (Sipes) was 135,000ppm and the maximum for the USA-affiliated brand (Dutch Boy) was 32,400ppm. Lead was not detected in any paints from the three of the four brands of paint purchased in Paraguay that had headquarters/affiliations in other countries (Brazil-Coralit), Germany (Suvinil) and USA (Novacor)). Two of the three paints from each of the other Paraguay brands contained high levels of lead with the maximum concentrations of 108,000 and 168,000ppm; one of these brands was manufactured under a license from ICI in the Netherlands. All of the paints purchased in Russia were from Russian brands and were manufactured in Russia. All three paints from one brand contained below detection levels of lead. The maximum levels of lead in the other six brands in Russia ranged from 3230 to 52,900ppm. The two brands with the highest lead concentration, TEKS and LAKRA, were produced by companies in the top three in market share.. Overall, lead concentrations were much higher in the colored paints such as red and yellow than in white paints. In each of the three countries a brand based in that country had a colored paint that either met a 90ppm limit or was close to meeting the limit-demonstrating that practical technology was available in each of these countries to produce low lead bright colored enamel decorative paints. Even though technology for producing paint without added lead existed in each of these countries, twenty-nine (29) percent of the paints analyzed contained exceedingly high concentrations (>=10,000ppm) of lead.

Single-substance and mixture toxicity of five pharmaceuticals and personal care products to marine periphyton communities.

The single-substance and mixture toxicity of five pharmaceuticals and personal care products (fluoxetine, propranolol, triclosan, zinc-pyrithione, and clotrimazole) to marine microalgal communities (periphyton) was investigated. All compounds proved to be toxic, with median effective concentration values (EC50s) between 1,800 nmol/L (triclosan) and 7.2 nmol/L (Zn-pyrithione). With an EC50 of 356 nmol/L, the toxicity of the mixture falls into this span, indicating the absence of strong synergisms or antagonisms. In fact, a comparison with mixture toxicity predictions by the classical mixture concepts of concentration addition and independent action showed a good predictability in the upper effect range. However, the mixture provoked stimulating effects (hormesis) in the lower effect range, hampering the application of either concept. An independent repetition of the mixture experiment resulted in a principally similar concentration-response curve, again with clear hormesis effects in the lower range of test concentrations. However, the curve was shifted toward higher effect concentrations (EC50 1,070 nmol/L), which likely is due to changes in the initial species composition. Clear mixture effects were observed even when all five components were present only at their individual no-observed-effect concentrations (NOECs). These results show that, even with respect to mixtures of chemically and functionally dissimilar compounds, such as the five pharmaceuticals and personal care products investigated, environmental quality standards must take possible mixture effects from low-effect concentrations of individual compounds into consideration.

Toxicity of five protein synthesis inhibiting antibiotics and their mixture to limnic bacterial communities.

Antibiotics are common contaminants of aquatic environments, the protein synthesis inhibitors being one frequently detected class. Even though antibiotics target bacteria, little is known about the sensitivity of naturally occurring freshwater bacteria to these compounds. Limnic bacterial communities were therefore systematically exposed to five common protein synthesis inhibiting antibiotics, each representing a particular subgroup: streptomycin, chloramphenicol, fusidic acid, rifampicin and chlortetracycline. Full concentration-response curves and No Observed Effect Concentrations (NOECs) were determined for all antibiotics, using the (3H)leucine incorporation method. All test compounds were toxic to planktonic communities of limnic bacteria, with EC50s ranging from 0.138 micromol/L for chlortetracycline to 79.1 micromol/L for streptomycin. The order of toxicity was chlortetracycline>rifampicin>fusidic acid>chloramphenicol>streptomycin, based on the individual EC50 values. A comparison to reported chemical monitoring data shows that environmental concentrations of chlortetracycline are in a range that clearly inhibits the protein biosynthesis activity of planktonic bacterial communities. All compounds show exceptionally flat concentration-response relationship, for fusidic acid the ratio of EC50 to EC05 exceeds four orders of magnitude. This challenges the standard assessment factors of 10-100 for the extrapolation from high to low doses. Environmental exposure situations are often characterized by the presence of mixtures of antibiotics, e.g. in sewage effluents or river systems. Hence, also combined effects of the five antibiotics were determined, and compared to mixture toxicity predictions based on Concentration Addition and Independent Action. Concentration Addition slightly underestimated the observed EC50 by a factor of 1.5, independent on whether the prediction was based on single substance data that were recorded in parallel or whether historical data were used. Independent Action predicted higher mixture toxicity than Concentration Addition due to the flatness of the individual concentration-response curves. Implications of these findings for the environmental risk assessment of antibiotics and their mixtures are discussed.

An open source chimera checker for the fungal ITS region.

The internal transcribed spacer (ITS) region of the nuclear ribosomal repeat unit holds a central position in the pursuit of the taxonomic affiliation of fungi recovered through environmental sampling. Newly generated fungal ITS sequences are typically compared against the International Nucleotide Sequence Databases for a species or genus name using the sequence similarity software suite blast. Such searches are not without complications however, and one of them is the presence of chimeric entries among the query or reference sequences. Chimeras are artificial sequences, generated unintentionally during the polymerase chain reaction step, that feature sequence data from two (or possibly more) distinct species. Available software solutions for chimera control do not readily target the fungal ITS region, but the present study introduces a blast-based open source software package (available at http://www.emerencia.org/chimerachecker.html) to examine newly generated fungal ITS sequences for the presence of potentially chimeric elements in batch mode. We used the software package on a random set of 12 300 environmental fungal ITS sequences in the public sequence databases and found 1.5% of the entries to be chimeric at the ordinal level after manual verification of the results. The proportion of chimeras in the sequence databases can be hypothesized to increase as emerging sequencing technologies drawing from pooled DNA samples are becoming important tools in molecular ecology research.