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Biomass burning is a significant anthropogenic source of air pollution, including the preharvest burning of sugar cane. These burn events result in atmospheric emissions, including semivolatile organic compounds, that may have adverse impacts on air quality and human health on a local, regional, and even a global scale. Gaseous and particulate polycyclic aromatic hydrocarbon (PAH) emissions from various sugar cane burn events in the province of Kwa‐Zulu Natal in South Africa were simultaneously sampled using a portable denuder sampling technology, consisting of a quartz fiber filter sandwiched between two polydimethylsiloxane multichannel traps. Total gas and particle phase PAH concentrations ranged from 0.05 to 9.85 µg m–3 per individual burn event, and nine PAHs were quantified. Over 85% of all PAHs were found to exist in the gas phase, with smaller two‐ and three‐ring PAHs, primarily naphthalene, 1‐methyl naphthalene, and acenaphthylene, being the most dominant and causing the majority of variance between the burn sites. The PAH profiles differed between the different burn events at different sites, emphasizing the significant influence that the crop variety, prevailing weather conditions, and geographical location has on the type and number of pollutants emitted. The potential carcinogenicity of the PAH exposure was estimated based on toxic equivalency factors that showed varying risk potentials per burn event, with the highest value of 5.97 ng m–3. Environ Toxicol Chem 2023;42:778–792. © 2023 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC. [ABSTRACT FROM AUTHOR]

To assess the two most toxicologically relevant species of As, namely arsenite (As(III)) and arsenate (As(V)), chromatographic separations often require two separate chromatographic columns to address the co-elution of arsenobetaine (AsB) with As(III). This issue is typically observed using conventional isocratic methods on anion exchange columns, increasing cost and analysis time. Here, we optimize the extraction of inorganic As from a lichen air biomonitor and develop an isocratic method for the chromatographic separation of five common As species on a PRP X-100 anion exchange column, resulting in the complete baseline separation of all species under study. This method was then applied to lichen biomonitors from an urban and rural site to demonstrate its use. In order of abundance, the various arsenic species in lichens from the urban site in South Africa were As(V) > As(III) > AsB > dimethylarsinic acid (DMA) > monomethylarsonic acid (MMA), and As(V) > AsB > As(III) > DMA > MMA for the rural site, where MMA was present in extremely low, non-quantifiable concentrations in lichens from both sites. Total concentrations of As were higher in samples from the urban site (6.43 ± 0.25 μg/g) than in those from the rural site (1.87 ± 0.05 μg/g), with an overall extraction efficiency of 19% and 40%, respectively. The optimized method utilized relatively inexpensive solvents and is therefore low-cost and eco-friendly in comparison with conventional chromatographic techniques. This is the first study which addresses the optimized extraction and characterization of As species in a South African lichen biomonitor of air pollution. [ABSTRACT FROM AUTHOR]

Air dispersion software models for evaluating pesticide spray drift during application have been developed that can potentially serve as a cheaper convenient alternative to field monitoring campaigns. Such models require validation against field monitoring data in order for them to be employed with confidence, especially when they are used to implement regulatory measures or to evaluate potential human exposure levels. In this case study, off-target pesticide drift was monitored during ground application of a pesticide mixture to a sorghum field in South Africa. Atrazine was used as a drift tracer. High volume air sampling onto polyurethane foam (PUF) was conducted at six downwind locations and at four heights at each sampling point. Additional data, including meteorological information, required to simulate the spray drift with the AGDISP® air dispersion model was collected. The PUF plugs were extracted by a plunger method utilizing a hexane:acetone mixture with analysis by GC-NPD (94.5% recovery, 3.3% RSD, and LOD 8.7 pg). Atrazine concentrations ranged from 4.55 ng L(-1) adjacent to the field to 186 pg L(-1) at 400 m downwind. These results compared favourably with modeled output data, resulting in the validation of the model up to 400 m from the application site for the first time. Sensitivity studies showed the importance of droplet size distribution on spray drift, which highlighted the need for good nozzle maintenance. Results of this case study indicate that the model may provide meaningful input into environmental and human health risk assessment studies in South Africa and other developing countries., (Copyright © 2015 Elsevier Ltd. All rights reserved.)