A total of 106 24-h PM₂.₅ aerosol samples were collected in an urban area (Shijiazhuang, SJZ) and a suburban area (Liulihe, LLH, Fangshan County, Beijing) in the Beijing-Tianjin-Hebei (BTH) region in 2 periods: the first is from 10 July to 10 August, which is before Sept. Third Parade (Period I); the second is from 20 Aug. to 6 Sept. 2015, which is during Sept. Third Parade (Period II). Polar organic tracers, including isoprene, α-pinene, β-caryophyllene and toluene oxidation products, as well as sugars and carboxylic acids were measured. In Period II, rigorous emission-reduction measures were taken in the BTH region. With the anthropogenic emission being cut down significantly, the average concentrations of isoprene, α-pinene, β-caryophyllene and toluene oxidation products and all carboxylic acids (except tetradecanoic, palmitic, and stearic acids), were lower in Period II than those in Period I in LLH, indicating that the SOA tracers were decreased with precursor emission volumes and yields in the atmosphere. Moreover, sugar compounds were shown with comparable levels during the two periods in LLH, suggesting that no measures were taken to reduce the intensities of the biogenic sources. On the contrary, tetradecanoic, palmitic, and stearic acids were shown with obviously higher concentrations in Period II than those in Period I, demonstrating that cooking fumes increased during Sept. Third Parade period.The positive matrix factorization (PMF) model combining with tracer-based method was applied to explore the sources of secondary organic carbon (SOC). It reveals that the sources of SOC include isoprene, α-pinene, β-caryophyllene and toluene oxidation products, fossil fuel combustion, cooking fumes and regionally transferred aged aerosols. These sources accounted for 11.3%, 9.0%, 15.5%, 10.9%, 29.2%, 2.9%, 21.1% of SOC for SJZ, and 12.7%, 11.2%, 9.7%, 14.4%, 25.3%, 0%, 26.7% of SOC for LLH, during the whole sampling periods respectively.

A comprehensive modelling approach has been developed to predict population exposure to the ambient air PM₂.₅ concentrations in different microenvironments in London. The modelling approach integrates air pollution dispersion and exposure assessment, including treatment of the locations and time activity of the population in three microenvironments, namely, residential, work and transport, based on national demographic information. The approach also includes differences between urban centre and suburban areas of London by taking account of the population movements and the infiltration of PM₂.₅ from outdoor to indoor. The approach is tested comprehensively by modelling ambient air concentrations of PM₂.₅ at street scale for the year 2008, including both regional and urban contributions. Model analysis of the exposure in the three microenvironments shows that most of the total exposure, 85%, occurred at home and work microenvironments and 15% in the transport microenvironment. However, the annual population weighted mean (PWM) concentrations of PM₂.₅ for London in transport microenvironments were almost twice as high (corresponding to 13–20 μg/m³) as those for home and work environments (7–12 μg/m³). Analysis has shown that the PWM PM₂.₅ concentrations in central London were almost 20% higher than in the surrounding suburban areas. Moreover, the population exposure in the central London per unit area was almost three times higher than that in suburban regions. The exposure resulting from all activities, including outdoor to indoor infiltration, was about 20% higher, when compared with the corresponding value obtained assuming inside home exposure for all times. The exposure assessment methodology used in this study predicted approximately over one quarter (−28%) lower population exposure, compared with using simply outdoor concentrations at residential locations. An important implication of this study is that for estimating population exposure, one needs to consider the population movements, and the infiltration of pollution from outdoors to indoors.

Microplastic pollution has become an emergency issue in the global environment. However, little is known about the occurrence and distribution of microplastics in agroecological system. In this study, we investigated the pollution of microplastics in vegetable farmlands in suburb of Wuhan, central China. Results showed that the abundance of microplastics ranged from 320 to 12,560 items/kgdw. Microplastic pollution adjacent to the suburban roads was about 1.8 times as serious as that in the residential areas. Microplastics with size less than 0.2 mm were dominated, reaching 70% in total. The main types of microplastics were fibers and microbeads. Moreover, polyamide (32.5%) and polypropylene (28.8%) were the main types of polymer. This study proclaims the occurrence and characteristics of microplastic pollution in typical farmland soils of suburb land. It may provide significant basis for subsequent research about microplastics contaminant in the terrestrial ecosystem.

Destructive development of suburban areas in some metropolises has exposed suburban soils to high risk of potentially toxic trace elements (PTEs) enrichment, which also threatens human and ecosystem health. This study investigated the pollution status, sources and spatial patterns of four PTEs (Pb, Cd, Cr and As) in 1805 soil samples collected from the suburbs of Shanghai in 2015. Nineteen potential sources, including: 6 soil property factors, 10 proximity factors and 3 topography factors, were selected to help explain the PTEs aggregation using logistic regression models from global and local perspectives. The statistical results of PTEs concentration revealed that Cd showed the highest pollution risk in local soils, which was followed by As. Soil property was the primary factor affecting the PTEs (except Cr) enrichment, both identified by global models and local models. The local model particularly emphasized the significant correlation between soil property and PTEs in most parts of the outer suburbs and southeastern inner suburbs. Some proximity factors such as distance to district center and water were negatively correlated with Cd pollution and some topography factors such as elevation and slope were closely related to As pollution. It is worth noting that in the coastal areas, especially Chongming Island, there were obvious PTEs depositions in the soil near the estuary. This study helps to identify the sources of anthropogenic contamination and geogenic enrichment of the four PTEs and their spatial patterns, playing an essential role in formulating regional environmental policies for coastal cities.

Coal-Gas replacement project has been implemented to decrease haze pollution in China in recent years. Airborne arsenic (As) mostly originates from coal burning processes. It is noteworthy to compare the distribution of arsenic fraction in PM₂.₅ before and after coal-gas replacement. Eighty PM₂.₅ samples were collected in Baoding in December 2016 (coal dominated year) and December 2017 (gas dominated year) at different functional areas including residential area (RA), industrial area (IA), suburb (SB), roadside (ST) and Botanical Garden Park (BG). The fraction, bioavailability and health risk of As in the PM₂.₅ samples were investigated and compared between these two years. Arsenic was mainly distributed in the non-specifically sorbed fraction (F1) and the residual fraction (F5). However, the proportion of F1 to the total As in 2017 was higher than that in 2016, while the proportion of As in the amorphous and poorly-crystalline hydrous oxides of Fe and Al fraction (F3) in 2017 was lower. The distributions of fraction and bioavailability showed temporal and spatial characteristics. The total concentration and bioavailability of As in SB and IA were significantly higher than those in RA, ST and BG. The BF (Bioavailability Factor) values of As ranged from 0.30 to 0.61. Health risk assessment indicated that the hazard quotient (HQ) and carcinogenic risk (CR) of As in PM₂.₅ significantly decreased after coal-gas replacement.

In the study, personal PM₂.₅ exposures and their source contributions were characterized for 159 subjects living in the Beijing Metropolitan area. The exposures and sources were examined as functions of residential location, season, vocation, cigarette smoking, and time spent outdoors. Sampling was performed for two categories of volunteers, guards and students, that lived in urban and suburban areas of Beijing. Samples were collected using portable PM₂.₅ monitors during summer and winter. Exposure measurements were supplemented with a questionnaire that tracked personal activity and time spent in microenvironments that may have impacted exposures. Simultaneously, ambient PM₂.₅ data were obtained from national network stations located at the Gucheng and Huairouzhen sites. These data were used as a comparison against the personal PM₂.₅ exposures and produced poor correlations between personal and ambient PM₂.₅. These results demonstrate that individual behavior strongly affects personal PM₂.₅ exposure. Six primary sources of personal PM₂.₅ exposure were determined using a positive matrix factorization (PMF) source apportionment model. These sources included Roadway Transport Source, Soil/Dust Source, Industrial/Combustion Source, Secondary Inorganic Source, Cd Source, and Household Heating Source. Averaged across all subjects and seasons, the highest source contribution was Secondary Inorganic Source (24.8% ± 32.6%, AVG ± STD), whereas the largest primary ambient source was determined to be Roadway Transport (20.9% ± 13.6%). Subjects were classified according to the questionnaire and were used to help understand the relationship between personal activity and source contribution to PM₂.₅ exposure. In general, primary ambient sources showed only significant spatial and seasonal differences, while secondary sources differed significantly between populations with different personal behavior. In particular, Cd source was found to be related to smoking exposure and was the most unpredictable source, with significant differences between populations of different sites, vocations, smoking exposures, and outdoor time.

The concept of thresholds shows important implications for environmental and resource management. Here we derived potential landscape thresholds which indicated abrupt changes in water quality or the dividing points between exceeding and failing to meet national surface water quality standards for a rapidly urbanizing city on the Eastern Coast in China. The analysis of landscape thresholds was based on regression models linking each of the seven water quality variables to each of the six landscape metrics for this coupled land-water system. We found substantial and accelerating urban sprawl at the suburban areas between 2000 and 2008, and detected significant nonlinear relations between water quality and landscape pattern. This research demonstrated that a simple modeling technique could provide insights on environmental thresholds to support more-informed decision making in land use, water environmental and resilience management.

Rice and the distinctive cultivation practices employed in rice growth can significantly influence the environmental fate of polybrominated diphenyl ethers (PBDEs) in a paddy field. We studied variations in PBDE concentrations in multiple compartments of a paddy field in the suburban area of Guangzhou, South China, including air, soil, water, and rice tissues. The input/output fluxes of air–surface and air–foliage exchange, atmospheric deposition and water input during different rice growth stages were measured simultaneously. Air–foliage and air–water diffusion exchanges were the key processes controlling inputs and outputs of PBDEs in paddy fields, respectively, whereas atmospheric deposition dominated inputs of higher brominated PBDEs. The high input of PBDEs via air–foliage exchange suggested that vegetation can significantly increase the air-to-field transport of PBDEs in ecosystems. The annual input of PBDEs in all paddy fields in Guangdong Province was estimated to be 22.1 kg.

A set of toxic metals, i.e. As, Hg, Pb, Cd, Cu, Zn, Ni and Cr, in urban and suburban SDSs were investigated comparatively in the biggest metropolitan area of China, Shanghai. Results showed that all of the metals except As were accumulated greatly, much higher than background values. Geo-accumulation index indicated that metal contamination in urban SDSs was generally heavier than that in suburban SDSs. Potential ecological risk index demonstrated that overall risks caused by metals were considerable. Cd contributed 52% to the overall risk. Multivariate statistical analysis revealed that in urban SDSs, Zn, Ni, Cd, Pb, Cu and Cr were related to traffic and industry; coal combustion led to elevated levels of Hg; soil parent materials controlled As contents. In suburban SDSs, Pb, Cu, As and Cd largely originated from traffic pollution; Zn, Ni and Cr were associated with industrial contaminants; Hg was mainly from domestic solid waste. Sources and contamination characteristics of toxic metals in urban and suburban SDSs were different due to the varied levels of human activity intensity.

Microplastics (MPs) and microfibers (MFs) in stormwater have been poorly investigated. Data on their intra and inter rain events variability over time are still sparse. For the first time, the variability of microlitter concentrations in stormwater has been studied. MF and MP concentrations were investigated in stormwater runoff at the outlet of the suburban catchment at Sucy-en-Brie (a suburb of Paris, France), during four rain events. Median MF and MP concentrations were 1.9 and 29 items/L, with an interquartile range of 2.3 and 36 items/L, respectively (N = 18). A different pattern was observed between MFs and MPs. While no relationship or trends were observed for MFs, the highest MP concentrations were observed before the flow rate peak of the rain events. This could indicate a difference in the behaviour between MFs and MPs. We estimated the median MP mass concentration to be 56 μg/L with an interquartile range of 194 μg/L, whereas the mass concentration of macroplastics was estimated to be 31 μg/L with an interquartile range of 22 μg/L at the same sampling site, in a previous study. For this sampling site, MPs and macroplastics have the same order of magnitude. This study may have strong implications on microplastic assessment in urban waters.