Lichens serve as important bioindicators of air pollution in cities. Here, we studied the diversity of epiphytic lichens in the urban area of Munich, Bavaria, southern Germany, to determine which factors influence species composition and diversity. Lichen diversity was quantified in altogether 18 plots and within each, five deciduous trees were investigated belonging to on average three tree species (range 1–5). Of the 18 plots, two were sampled in control areas in remote areas of southern Germany. For each lichen species, frequency of occurrence was determined in 10 quadrats of 100 cm² on the tree trunk. Moreover, the cover percentage of bryophytes was determined and used as a variable to represent potential biotic competition. We related our diversity data (species richness, Shannon index, evenness, abundance) to various environmental variables including tree traits, i.e. bark pH levels and species affiliation and air pollution data, i.e. NO₂ and SO₂ concentrations measured in the study plots. The SO₂ levels measured in our study were generally very low, while NO₂ levels were rather high in some plots. We found that the species composition of the epiphytic lichen communities was driven mainly by NO₂ pollution levels and all of the most common species in our study were nitrophilous lichens. Low NO₂ but high SO₂ values were associated with high lichen evenness. Tree-level lichen diversity and abundance were mainly determined by tree traits, not air pollution. These results confirm that ongoing NO₂ air pollution within cities is a major threat to lichen diversity, with non-nitrophilous lichens likely experiencing the greatest risk of local extinctions in urban areas in the future. Our study moreover highlights the importance of large urban green spaces for species diversity. City planners need to include large green spaces when designing urban areas, both to improve biodiversity and to promote human health and wellbeing.

Little is known about the main sources of ambient particulate matter (PM) in the 22 Eastern Mediterranean Region (EMR) countries. We designed this study to systematically review all published and unpublished source apportionment (SA), identification and characterization studies as well as emission inventories in the EMR. Of 440 articles identified, 82 (11 emission inventory ones) met our inclusion criteria for final analyses. Of 22 EMR countries, Iran with 30 articles had the highest number of studies on source specific PM followed by Pakistan (n = 15 articles) and Saudi Arabia (n = 8 papers). By contrast, there were no studies in Afghanistan, Bahrain, Djibouti, Libya, Somalia, Sudan, Syria, Tunisia, United Arab Emirates and Yemen. Approximately 72% of studies (51) were published within a span of 2015–2021.48 studies identified the sources of PM₂.₅ and its constituents. Positive matrix factorization (PMF), principal component analysis (PCA) and chemical mass balance (CMB) were the most common approaches to identify the source contributions of ambient PM. Both secondary aerosols and dust, with 12–51% and 8–80% (33% and 30% for all EMR countries, on average) had the greatest contributions in ambient PM₂.₅. The remaining sources for ambient PM₂.₅, including mixed sources (traffic, industry and residential (TIR)), traffic, industries, biomass burning, and sea salt were in the range of approximately 4–69%, 4–49%, 1–53%, 7–25% and 3–29%, respectively. For PM₁₀, the most dominant source was dust with 7–95% (49% for all EMR countries, on average). The limited number of SA studies in the EMR countries (one study per approximately 9.6 million people) in comparison to Europe and North America (1 study per 4.3 and 2.1 million people respectively) can be augmented by future studies that will provide a better understanding of emission sources in the urban environment.

Microplastics (MPs) are an emerging pollutant and a worldwide issue. A wide variety of MPs and tyre wear particles (TWPs) are entering and spreading in the environment. TWPs can reach waterbodies through runoff, where main contributing particulate matter comes from impervious areas. In this paper, TWPs and other types of MPs that were transported with the runoff of a high populated-impervious urban area were characterised. Briefly, MPs were sampled from sediments in a stormwater detention reservoir (SDR) used for flood control of a catchment area of ∼36 km², of which 73% was impervious. The sampled SDR is located in São Paulo, the most populated city in South America. TWPs were the most common type of MPs in this SDR, accounting for 53% of the total MPs; followed by fragments (30%), fibres (9%), films (4%) and pellets (4%). In particular, MPs in the size range 0.1 mm–0.5 mm were mostly TWPs. Such a profile of MPs in the SDR is unlike what is reported in environmental compartments elsewhere. TWPs were found at levels of 2160 units/(kg sediment·km² of impervious area) and 87.8 units/(kg sediment·km street length); MP and TWP loadings are introduced here for the first time. The annual flux of MPs and TWPs were 7.8 × 10¹¹ and 4.1 × 10¹¹ units/(km²·year), respectively, and TWP emissions varied from 43.3 to 205.5 kg/day. SDRs can be sites to intercept MP pollution in urban areas. This study suggests that future research on MP monitoring in urban areas and design should consider both imperviousness and street length as important factors to normalize TWP contribution to urban pollution.

Microplastics (MPs) have elicited increasing concerns in freshwater systems worldwide. However, little information is available on the MP pollution in the Songhua River, the third largest river in China. And the understanding of the sources and pathways of MPs is limited. In this study, MPs were sampled from river water and wastewater treatment plants in five cities along the Songhua River to investigate the occurrence, spatial distribution, characteristics, and potential sources of MPs. Polyethylene, polypropylene and polystyrene accounted for more than 95% of the total MPs. MP pollution was determined to be spatially heterogeneous. The concentration of MPs in the urban center was always considerably higher than that in the upper reach, and irregular variation was observed from the urban center to the lower reach for each city. Urbanization was one of the primary driving forces of spatial variability. Statistically significant positive correlations (p-value < 0.05) were noted between the average concentration of MPs in river water and population density (p = 0.0023) and number of industrial enterprises above designated size (p = 0.0042) of each city. Line and fiber were the major shapes, and white was the most dominant color. Large (1–5 mm) and small (≤ 1 mm) MP particles accounted for 50% each. Multiple correspondence analysis as a new methodological approach was conducted to elucidate the sources of MPs for the first time. The potential sources of MPs included daily use, fishing, agricultural, and industrial productions. This work provides information about MP contamination for future studies on freshwater systems and new insights into the source apportionment of MPs.

Cities constitute an important source of greenhouse gases, but few results originating from long-term, direct CO₂ emission monitoring efforts have been reported. In this study, CO₂ emissions were quasi-continuously measured in an urban center in Sakai, Osaka, Japan by the eddy covariance method from 2010 to 2021. Long-term CO₂ emissions reached 22.2 ± 2.0 kg CO₂ m⁻² yr⁻¹ from 2010 to 2019 (± denotes the standard deviation) in the western sector from the tower representing the densely built-up area. Throughout the decade, the annual CO₂ emissions remained stable. According to an emission inventory, traffic emissions represented the major source of CO₂ emissions within the flux footprint. The interannual variations in the annual CO₂ flux were positively correlated with the mean annual traffic counts at two highway entrances and exits. The CO₂ emissions decreased suddenly, by 32% ± 3.1%, in April and May 2020 during the period in which the first state of emergency associated with COVID-19 was declared. The annual CO₂ emissions also decreased by 25% ± 3.1% in 2020. Direct long-term observations of CO₂ emissions comprise a useful tool to monitor future emission reductions and sudden disruptions in emissions, such as those beginning in 2020 during the COVID-19 pandemic.

Lichens play an important role in the biogeochemical cycling of mercury (Hg) and are commonly used as indicators of Hg enrichment in remote and anthropogenically impacted environments. To assess their capacity for Hg uptake and accumulation, we determined the concentration of gaseous elemental mercury (GEM) in air and the concentration of total Hg (THg) in transplanted thalli of two lichen species. Lichen transplants and passive air samplers (PASs) were concurrently deployed, side by side, at 10 sites within an abandoned mining area, characterized by large gradients in atmospheric Hg contamination. Highly variable time-weighted GEM concentrations determined by the PASs, ranging from 17 to 4,200 ng/m³, were mirrored by generally high Hg concentrations in transplanted thalli of both Xanthoria parietina (174–8,800 ng/g) and Evernia prunastri (143–5,500 ng/g). Hg concentrations in the two species co-varied linearly indicating about 60% greater Hg accumulation in X. parietina than in E. prunastri. Whereas Hg uptake in the fruticose E. prunastri increased linearly with GEM, a power law equation with a fractional exponent described the uptake in the foliose X. parietina. Extrapolating the relationships observed here to higher GEM levels yielded concentrations in lichen that agree very well with those measured in an earlier fumigation experiment performed under laboratory-controlled conditions. The uptake model of X. parietina was further verified by correctly estimating GEM concentrations from the THg measured in autochthonous thalli collected from the urban area adjacent to the mine site. Passive sampling can effectively provide time-weighted data of suitable spatial resolution to quantitatively describe GEM assimilation by lichens. Therefore, the combined use of passive sampling and lichen transplants can contribute to a more comprehensive understanding of the role of lichens, and potentially also of other cryptogams, in the deposition of atmospheric Hg to terrestrial ecosystems.

This study investigated the hourly inorganic aerosol chemistry and its impact on atmospheric visibility over an urban area in Central Taiwan, by relying on measurements of aerosol light extinction, inorganic gases, and PM₂.₅ water-soluble ions (WSIs), and simulations from a thermodynamic equilibrium model. On average, the sulfate (SO₄²⁻), nitrate (NO₃⁻), and ammonium (NH₄⁺) components (SNA) contributed ∼90% of WSI concentrations, which in turn made up about 50% of the PM₂.₅ mass. During the entire observation period, PM₂.₅ and SNA concentrations, aerosol pH, aerosol liquid water content (ALWC), and sulfur and nitrogen conversion ratios all increased with decreasing visibility. In particular, the NO₃⁻ contribution to PM₂.₅ increased, whereas the SO₄²⁻ contribution decreased, with decreasing visibility. The diurnal variations of the above parameters indicate that the interaction and likely mutual promotion between NO₃⁻ and ALWC enhanced the hygroscopicity and aqueous-phase reactions conducive for NO₃⁻ formation, thus led to severely impaired visibility. The high relative humidity (RH) at the study area (average 70.7%) was a necessary but not sole factor leading to enhanced NO₃⁻ formation, which was more directly associated with elevated ALWC and aerosol pH. Simulations from the thermodynamic model depict that the inorganic aerosol system in the study area was characterized by fully neutralized SO₄²⁻ (i.e. a saturated factor in visibility reduction) and excess NH₄⁺ amidst a NH₃-rich environment. As a result, PM₂.₅ composition was most sensitive to gas-phase HNO₃, and hence NOx, and relatively insensitive to NH₃. Consequently, a reduction of NOx would result in instantaneous cuts of NO₃⁻, PM₂.₅, and ALWC, and hence improved visibility. On the other hand, a substantial amount of NH₃ reduction (>70%) would be required to lower the aerosol pH, driving more than 50% of the particulate phase NO₃⁻ to the gas phase, thereby making NH₃ a limiting factor in shifting PM₂.₅ composition.

Estuaries are considered as important sources of the global emission of greenhouse gases (GHGs). Urbanized estuaries often experience eutrophication under strong anthropogenic activities. Eutrophication can enhance phytoplankton abundance, leading to carbon dioxide (CO₂) consumption in the water column. Only a few studies have evaluated the relationship between GHGs and eutrophication in estuaries. In this study, we assessed the concentrations and fluxes of CO₂, methane (CH₄) and nitrous oxide (N₂O) in combination with a suite of biogeochemical variables in four sampling campaigns over two years in a highly urbanized tropical estuary in Southeast Asia (the Saigon River Estuary, Vietnam). The impact of eutrophication on GHGs was evaluated through several statistical methods and interpreted by biological processes. The average concentrations of CO₂, CH₄ and N₂O at the Saigon River in 2019–2020 were 3174 ± 1725 μgC-CO₂ L⁻¹, 5.9 ± 16.8 μgC-CH₄ L⁻¹ and 3.0 ± 4.8 μgN-N₂O L⁻¹, respectively. Their concentrations were 13–18 times, 52–332 times, and 9–37 times higher than the global mean concentrations of GHGs, respectively. While CO₂ concentration had no clear seasonal pattern, N₂O and CH₄ concentrations significantly differed between the dry and the rainy seasons. The increase in eutrophication status along the dense urban area was linearly correlated with the increase in GHGs concentrations. The presence of both nitrification and denitrification resulted in elevated N₂O concentrations in this urban area of the estuary. The high concentration of CO₂ was contributed by the high concentration of organic carbon and mineralization process. GHGs fluxes at the Saigon River Estuary were comparable to other urbanized estuaries regardless of climatic condition. Control of eutrophication in urbanized estuaries through the implantation of efficient wastewater treatment facilities will be an effective solution in mitigating the global warming potential caused by estuarine emissions.

An increasing body of evidence has linked greenspace and various health outcomes in children and adolescents, but the conclusions were inconsistent. For this review, we comprehensively summarized the measurement methods of greenspace, resultant health outcomes, and potential mechanisms from epidemiological studies in children and adolescents (aged ≤19 years). We searched for studies published and indexed in MEDLINE and EMBASE (via Ovid) up to April 11, 2022. There were a total of 9,291 studies identified with 140 articles from 28 countries finally assessed and included in this systematic review. Over 70% of the studies were conducted in highly urbanised countries/regions, but very limited research has been done in low-and middle-income countries and none in Africa. Measures of greenspace varied. Various health outcomes were reported, including protective effects of greenspace exposure on aspects of obesity/overweight, myopia, lung health, circulatory health, cognitive function, and general health in children and adolescents. The associations between greenspace exposure and other health outcomes were inconsistent, especially for respiratory health studies. We pooled odds ratios (OR) using random-effects meta-analysis for health outcomes of asthma (OR = 0.94, 95%CI: 0.84 to 1.06), allergic rhinitis (OR = 0.95; 95% CI: 0.73 to 1.25), and obesity/overweight (OR = 0.91, 95%CI: 0.84 to 0.98) with per 0.1 unit increase in normalized difference in vegetation index (NDVI). These associations have important implications for the assessment and management of urban environment and health in children and adolescents.

Size-fractionated particulate matters (SPMs) in a range of 9.0 to 0.43 μm, classified based on aerodynamic diameter (dₐₑ) as fine PMs (0.43 μm ≤ dₐₑ < 2.1 μm) and coarse PMs (2.1 μm ≤ dₐₑ < 9.0 μm) were collected by cascade impactors (7 fractions) during smoke haze (SH) and non-smoke haze (NSH) seasons in urban and rural areas of Chiang Mai, Thailand. Their polycyclic aromatic hydrocarbons (PAHs) compositions were determined for respiratory health risk assessment. During SH episode, concentrations of SPMs and PAHs in the rural area were approximately two times higher than in the urban area and about 62–68% of the SPMs were fine particles. Conversely, during NSH season the concentrations in the urban area were higher due to traffic emission. The finest particle sizes (0.65–0.43 μm) contained the highest PAHs concentrations among the other PM sizes. Benzo[b]fluoranthene was a main PAH component found during SH season suggesting biomass burning is a major pollutant source. High molecular weight (5–6 rings) PAHs with high carcinogenicity were likely to concentrate in fine particles. Distribution patterns of SPMs and PAHs during SH season were bimodal with the highest peak at a fine size range (0.65–0.43 μm) and a small peak at a coarse size range (5.8–4.7 μm). Respiratory health risk was estimated based on toxicity equivalent concentrations of PAHs bound-SPMs and inhalation cancer risk (ICR). Relatively high ICR values (1.14 × 10⁻⁴ (rural) and 6.80 × 10⁻⁵ (urban)) were found during SH season in both areas, in which fine particles played an important role. It revealed that high concentration of fine particles in ambient air is related to high respiratory health risk due to high content of carcinogenic substances.