Small aethalometers are frequently used to measure equivalent black carbon (eBC) mass concentrations in the context of personal exposure and air pollution mapping through mobile measurements (MM). The most widely used is the microAethalometer (AE51). Its performance in the laboratory and field is well documented, however, there is not sufficient data in the context of its performance in different environments. In this investigation, we present the characterization of the performance of the AE51 through field unit-to-unit intercomparisons (IC), and against a reference absorption photometer from three MM campaigns conducted in drastically different environments. Five IC parameters were considered: i) study area, ii) location of IC, iii) time of day, iv) duration of IC, and v) correction for the filter-loading effect. We can conclude that it is crucial where and how long the IC have been performed in terms of the correlation between the mobile and reference instruments. Better correlations (R 2 > 0.8, slope = 0.8) are achieved for IC performed in rural, and background areas for more than 10 minutes. In locations with more homogenous atmosphere, the correction of the loading effect improved the correlation between the mobile and reference instruments. In addition, a newer microAethalometer model (MA200) was characterized in the field under extreme cold conditions and correlated against another MA200 (R 2 > 0.8, slope ≈ 1.0), AE51(R 2 > 0.9, slope ≈ 0.9), and a stationary Aethalometer (AE33) across all wavelengths (R 2 > 0.8, slope ≈ 0.7). For MA200, the loading effect was more pronounced, especially at the lower wavelengths, hence the correction of the loading effect is essential to improve the correlation against the AE33. The MA200 and AE51 proved to be robust and dependable portable instruments for MM applications. Real-world quality assurance of these instruments should be performed through field IC against reference instruments with longer durations in areas of slowly changing eBC concentration.
Biogenic fraction of airborne PM10 which includes bacteria, viruses, fungi and pollens, has been proposed as one of the potential causes of the PM10 toxicity. The present study aimed to provide a comprehensive understanding of the microbial community variations associated to PM10, and their main local sources in the surrounding environment in three urban sites of Rome, characterized by differential pollution rate: green area, residential area and polluted area close to the traffic roads. We combined high-throughput amplicon sequencing of the bacterial 16S rRNA gene and the fungal internal transcribed spacer (ITS) region, with detailed chemical analysis of particulate matter sampled from air, paved road surfaces and leaf surfaces of Quercus ilex. Our results demonstrated that bacterial and fungal airborne communities were characterized by the highest alpha-diversity and grouped separately from epiphytic and road dust communities. The reconstruction of source-sink relationships revealed that the resuspension/deposition of road dust from traffic might contribute to the maximum magnitude of microbial exchanges. The relative abundance of extremotolerant microbes was found to be enhanced in epiphytic communities and was associated to a progressively increase of pollution levels as well as opportunistic human pathogenicity in fungal communities.
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