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Lagoon water, suspended particulate matter, and sediment samples from seven sites at Lagoon of Venice were collected from 2019 to 2021 in order to study the presence of the herbicide glyphosate ( N -(phosphonomethyl)glycine), among the most widely used agricultural chemicals worldwide, but its occurrence in lagoon water environment has not been deeply investigated. The sites were selected considering a supposed diversity of inputs and of pollution levels. An analytical method based on ion chromatography coupled with tandem mass spectrometry was optimized and validated for lagoon water, marine particulate matter, and sediment samples. Maximum concentrations of glyphosate were 260 and 7 ng L −1 for lagoon water and suspended particulate matter, respectively, and 15 ng g −1 for sediment, with some spatial and temporal fluctuations. Our results demonstrate that glyphosate content in the Venice Lagoon mainly depends on external forcing from river inlets and agricultural lagoon activities.

COVID-19 pandemic raised a debate regarding the role of airborne transmission. Information regarding virus-laden aerosol concentrations is still scarce in community indoors and what are the risks for general public and the efficiency of restriction policies. This work investigates, for the first time in Italy, the presence of SARS-CoV-2 RNA in air samples collected in different community indoors (one train station, two food markets, one canteen, one shopping centre, one hair salon, and one pharmacy) in three Italian cities: metropolitan city of Venice (NE of Italy), Bologna (central Italy), and Lecce (SE of Italy). Air samples were collected during the maximum spread of the second wave of pandemic in Italy (November and December 2020). All collected samples tested negative for the presence of SARS-CoV-2, using both real-time RT-PCR and ddPCR, and no significant differences were observed comparing samples taken with and without customers. Modelling average concentrations, using influx of customers’ data and local epidemiological information, indicated low values (i.e. < 0.8 copies m −3 when cotton facemasks are used and even lower for surgical facemasks). The results, even if with some limitations, suggest that the restrictive policies enforced could effectively reduce the risk of airborne transmissions in the community indoor investigated, providing that physical distance is respected.

Plant protection products are necessary to guarantee food security, but their drift into the environment, usually in the form of aerosol, poses a threat to the health of bystanders and surrounding ecosystems. Appropriate testing of plant protection equipment and of its possible configurations is key to reducing drift while guaranteeing treatment efficacy. A key role in drift generation and treatment quality is played by the drop size distribution (DSD) of the employed spray nozzles. The DSD of nozzles can and should be tested before being employed by various methods. This paper recounts the recent experience in testing the DSD generated by two types of agricultural nozzles by an Oxford Lasers N60V Particle/Droplet Image Analysis (PDIA) system. The analyses put in place aimed at identifying the optimal instrument settings and adapting the methodology to the relevant ISO 25358:2018 standard. The cumulated DSD of the two nozzle types have then been fitted with a logistic function, with the aim to obtain nozzle performance models. The fitting has proven highly reliable, with correlation coefficients R2≥0.98. These models are a satisfactory starting point to compare the performance of different PPEs. In perspective, the fitted nozzle models can help bridge the mathematical gap with other aspects of PPE performance, such as aerosol generation and downwind transport.

The use of plant protection products (PPPs) has become fundamental to guarantee excellent field productivity. Nevertheless, their usage presents critical issues, such as the quantity of substances used, the relative toxicity, and the contamination of nearby fields caused by atmospheric drift. This study focuses on the characterization of aerosol droplets of PPPs produced by spraying a chemical marker, fluorescein, with an orchard airblast sprayer equipped with conventional hollow cone (HC) and anti-drift air inclusion (AI) nozzles, using a wind tunnel as a controlled environment. A particle/droplet image analysis was employed to study the droplet production of the nozzles, while a liquid chromatography tandem mass spectrometry (HPLC-MS/MS) analysis allowed us to evaluate samples collected using a cascade impactor located at 5 m, 10 m, and 20 m from the emission point. Overall, HC nozzles are very accurate at producing specific drop size distributions (DSDs), while AI nozzles produce a much wider DSD, concentrating the largest part of the distributed volume into droplets of a larger size. The marker concentration was much lower for the AI nozzles compared to the HC nozzles; moreover, the two nozzles show a similar trend in the coarse droplet range, while significantly differing in the fine droplet spectrum.

This study presents the year-round variability of the water-soluble fraction of trace elements (wsTE) and rare earth elements (wsREE) among size segregated airborne particulate matter samples collected at Ny-Ålesund in the Svalbard Archipelago from 26 February 2018 to 26 February 2019. Six different aerosol dimensional fractions were collected using a multi-stage Andersen impactor to better understand local and global circulation with the aim of disentangling the source of inorganic tracers from specific natural or anthropogenic sources. The wsTE and wsREE content, especially in the finest fractions in remote areas, is primarily related to long-range transport and it gives valuable information on (1) the global circulation, (2) the natural sources and (3) the contribution of human activities to aerosol composition. A Factor Analysis was applied to the dataset, including levoglucosan and methanesulfonic acid (MSA), to assess the possibility of using certain inorganic tracers as indicators of specific transport events or circulation regimes. We also investigate back-trajectories to determine potential source areas.

Iodine and bromine play central roles in polar atmospheric chemistry: iodine influences the atmospheric oxidative capacity and can generate cloud condensation nuclei, while bromine participates in ozone depletion reactions, known as bromine explosions. Here we present a very sensitive analytical method for Br and I speciation by coupling the ion chromatography system (IC) with an inductively coupled plasma sector field mass spectrometer (ICP-SFMS). We achieved sub-picogram-per gram (pg g−1) as limits of detection (LODs) ranging from 0.4 pg g−1 for I−, 0.8 pg g−1 for IO3−, 4 pg g−1 for Br−, and 1 pg g−1 for BrO3−, respectively. These values represent a decrease of up to 30 times compared to the LODs reported in other studies. The method was validated using deep snow samples from the Svalbard Islands, collected at the end of the polar night to quantify various oxidized compounds during their seasonal minimum. In the future, this method could prove useful in the paleoclimatic study of ice cores and snow, as well as in ice chemistry research.

The study about how tyre-derived particles can potentially worsen the water quality and how traffic pollution markers can affect the environment is crucial for environmental management. Road emissions are known to contribute to pollution in various environments, and benzothiazoles and their derivates can be used to trace pollutant inputs related to surface runoff in the aquatic system. A total of eight benzothiazoles were determined in highway stormwater runoff and road dust collected from February to August 2022 near Venice (Casale sul Sile, Veneto Region, Italy). A new analytical method was validated, by using an UHPLC system coupled to a mass spectrometer (triple quadrupole). The target compounds were determined in both dissolved phase and suspended particulate matter of runoff, and the road dust samples were divided into seven fractions depending on particle diameters to understand the fraction partitioning. The results indicate that 2-SO 3 H-BTH was the most concentrated benzothiazole in all the analysed substrates, suggesting tyre debris as the main source because it is usually used in the vulcanization process. 2-SO 3 H-BTH reached a mean concentration of 115 ± 59 µg L −1 , 4 ± 3 µg L −1 , and 411 ± 441 µg Kg −1 for dissolved phase, suspended particulate matter, and road dust, respectively, while 2-OH-BTH and BTH showed values about an order of magnitude lower. The size distribution of most BTHs suggests that they are distributed in the finest fraction of road dust. An exception was given by 2-SCNMeS-BTH being present only in particles with a diameter > 1 mm.

The study of aerosols in high mountain regions is essential because particulate matter can play a role in altering the energy balance of high mountain regions, and aerosols can accelerate glacier melting in high mountain areas by darkening the ice surface, reducing its reflectivity (albedo). Studying aerosols in high mountain areas provides insights into long-range transport of pollutants, atmospheric dynamics, and climate change impacts. These regions can serve as valuable observatories for studying atmospheric processes. The main aim of this paper is to define the main sources of aerosols over an entire year of sampling at the Col Margherita Atmospheric Observatory (MRG; 46°22′0.059′′ N, 11°47′30.911′′ E; 2543 m a.s.l.), a high-altitude background site in the eastern Italian Alps. Here, we discuss the potential origins of more than 100 chemical markers (major ions, water-soluble organic compounds, trace elements, and rare earth elements) using different approaches. Some diagnostic ratios were applied, but source apportionment using positive matrix factorization (PMF) was used to define the main inputs of PM10 collected at this high-altitude site, resulting in the identification of four factors: (1) Saharan dust events, (2) long-range marine/anthropogenic influence, (3) biogenic sources, and (4) biomass-burning and anthropogenic emissions. It can be inferred that, despite the distant location of the Col Margherita site, both regional pollution and long-range anthropogenic pollution have discernible effects on this area.

Understanding the chemical composition and sources of organic aerosol (OA) in the Arctic is critical given its importance for particle climate-relevant properties. This study presents a year-long analysis (May 2019–June 2020) of PM1 filter samples collected in Ny-Ålesund, Svalbard. A multi-instrumental approach is employed to characterize the comprehensive chemical composition of PM1, with a specific focus on its water-soluble organic fraction depicted combining proton nuclear magnetic resonance spectroscopy (H-NMR) and high-resolution time-of-flight aerosol mass spectrometry (HR-TOF-AMS), which provide complementary insights into the nature and structure of the organic aerosol classes characterizing the bulk OA mixture. Positive matrix factorization (PMF) source apportionment identifies consistent OA sources from the H-NMR and AMS datasets, showing a pronounced seasonality in their relative contributions to total OA mass. Winter–spring aerosol is dominated by long-range transport of Eurasian anthropogenic pollution (up to 70 %), while summer is characterized by biogenic aerosols from marine sources (up to 44 %), including sulfur compounds, amines, and fatty acids. Occasional summertime high OA loadings are associated with wildfire aerosols enriched in levoglucosan and humic-like substances (HULIS; averagely 27 %–28 %). Eventually, about 28 %–40 % of the OA mass is attributed to an unresolved mixture of extremely oxidized compounds of difficult specific source attribution. This integrated approach provides valuable insights into the seasonal dynamics of OA sources in the Arctic.

Abstract Due to urbanization and industrialization, water pollution is now one of the major environmental challenges of the twenty-first century. Considering the increasing of agricultural and non-agricultural settings in the last decades, the investigation of the relationship between such pesticides and urban stormwater is critical to understand how urban, residential, and industrialized areas can affect environmental safety. Recently, scientific interest has grown in stormwater chemical characterization with the aim to define its impacts in the environment and possibly to make it potable water. In this context, glyphosate, glufosinate, and their degradation products have been identified as the key knowledge gap for the chemical characterization of stormwater. Research investments are needed for a better understanding of the highly polar pesticides to estimate their load, source, and dispersion of urban runoff due to residential use of herbicides. Furthermore, a more comprehensive study of wet and dry deposition and spray drift should be considered for a correct evaluation of source apportionment.