Soil contamination in urban environment by trace metals is of public concerns. For better risk assessment, it is important to determine their background concentrations in urban soils. For this study, we determined the background concentrations of 9 trace metals including As, Ba, Cd, Co, Cu, Ni, Pb, Se, and Zn in 214 urban soils in Florida from two large cities (Orlando and Tampa) and 4 small cities (Clay County, Ocala, Pensacola and West Palm Beach). The objectives were to determine: 1) total concentrations of trace metals in urban soils in cities of different size; 2) compare background concentrations to Florida Soil Cleanup Target Levels (FSCTLs); and 3) determine their distribution and variability in urban soils via multivariate statistical analysis. Elemental concentrations in urban soils were variable, with Pb being the highest in 5 cities (165–552 mg kg⁻¹) and Zn being the highest concentration in Tampa (1,000 mg kg⁻¹). Besides, the As and Pb concentrations in some soils exceeded the FSCTL for residential sites at 2.1 mg kg⁻¹ As and 400 mg kg⁻¹ Pb. Among the cities, Clay County and Orlando had the lowest concentrations for most elements, with Cd, Co, and As being the lowest while Ba, Pb and Zn being the highest. Among all values, geometric means were the lowest while 95th percentile was the highest for all metals. Most 95th percentile values were 2–3 folds higher than the GM data, with Pb presenting the greatest difference, being 4 times greater than GM value (58.9 vs. 13.6 mg kg⁻¹). Still they were lower than FSCTL, with As exceeding FSCTL for residential sites at 2.1 mg kg⁻¹. In addition, the linear discriminate analysis showed distinct separation among the cities: Ocala (Ba & Ni) and Pensacola (As & Pb) were distinctly different from each other and from other cities with higher metal concentrations. The large variations among elemental concentrations showed the importance to establish proper background concentrations of trace metals in urban soils.

Potential toxic metal(loid)s (PTMs) in road dust are a major concern in relation to urban environmental quality. Identifying pollution hotspots and sources of PTMs is an essential prerequisite for pollution control and management. Herein, the concentrations, pollution and potential health risks of 8 PTMs (As, Cd, Co, Cu, Hg, Mo, Pb and Zn) in road dust from the highly urbanized areas of Nanjing were studied. Spatial occurrences and sources of PTMs were explored using geostatistics, principal component analysis (PCA) and local Moran’s index. The contamination factor (CF) results showed that Co was mainly natural in origin, while the other PTMs were polluted, with average CFs ranging from 1.4 to 11.0 as follows: Hg > Mo > Cd > Cu > Pb > Zn > As, indicating moderate to very high contamination. Except for Co and Hg, the other PTMs were heavily loaded on PC1, which explained 44.72% of the total variance. Combining the statistical results and distributions of potential sources, we deduced that industrial emissions dominated the spatial patterns of all polluted PTMs in road dust, which showed high levels in the northern parts of the study region and generally decreasing levels southwards. Moreover, Pb and Zn in the south-central area and Cd in the north-central area displayed hotspots, with maximum CFs of 5.5 (Pb), 4.2 (Zn) and 16.2 (Cd), which were related to additional automotive and railway braking emissions, respectively. The resuspension of legacy pesticides in soil is likely responsible for the As pollution hotspot in the southwestern part. Despite the high anthropogenic contributions (27% for As and 68–88% for the other metals) to the PTMs in road dust, their noncarcinogenic and carcinogenic health risks were rarely found for children and adults based on the values of the hazard index and carcinogenic risk index. However, attention still should be paid to the pollution hotspots in the northern region.

Atmospheric levels of chlorinated paraffins (CPs) at five remote, six rural and four urban sites in Australia were measured using XAD-2 passive air samplers (XAD-PAS). While long-chain CP (LCCP, C>₁₇) levels were below method detection limits (MDLs), short-chain CPs (SCCPs, C₁₀₋₁₃) and, for the first time, medium-chain CPs (MCCPs, C₁₄₋₁₇) and CPs with a carbon chain length of nine (CP–C9) were found at many sites (88%, 81% and 88%, respectively) across the Australian continent, representing a range of environmental conditions. Applying preliminary sampling rates of the XAD-PAS for CPs, gaseous CP levels in Australian air were <MDL-1.3 and <MDL-1.8 ng/m³ for ΣSCCPs and ΣMCCPs, respectively, with a significant decreasing trend from more densely to less densely populated areas. Atmospheric median levels in this study (0.37 and 0.47 ng/m³ for SCCPs and MCCPs, respectively) were at the lower end of the median range (0.32–10 and 3.0–4.2 ng/m³ for SCCPs and MCCPs, respectively) reported for CPs at predominantly urban or industrial sites elsewhere (apart from China and extremely remote sites such as Antarctica). Principal component analysis matched the SCCP and MCCP congener group patterns in samples with those found in commercial mixtures, indicating a prevalence of less chlorinated congener groups in the Australian atmosphere. Information about the Australian production, use and disposal of CPs as well as their levels in other environmental matrices, including humans, is needed for assessing their emissions, behaviour, fate and potential exposure.

Increasing indirect nitrous oxide (N₂O) emission from river networks as a result of enhanced human activities on landscapes has become a global issue, as N₂O has been widely recognized as an important ozone-depleting greenhouse gas. However, indirect N₂O emissions from different rivers, particularly for those that drain completely different landscapes, are poorly understood. Here, we investigated the spatial-temporal variability of N₂O emissions among the different rivers in the Chaohu Lake Basin of Eastern China. Our results showed that river reaches in urban watersheds are the hotspots of N₂O production, with a mean N₂O concentration of ∼410 nmol L⁻¹, which is 9–18 times greater than those mainly draining forested (23 nmol L⁻¹), agricultural (42 nmol L⁻¹) and mixed (45 nmol L⁻¹) landscapes. Riverine dissolved N₂O was generally supersaturated with respect to the atmosphere. Such N₂O saturation can best be explained by nitrogen availability, except for those in the forested watersheds, where dissolved oxygen is thought to be the primary predictor. The estimated N₂O fluxes in urban rivers reached ∼471 μmol m⁻² d⁻¹, a value of ∼22, 13, and 11 times that in forested, agricultural and mixed watersheds, respectively. Averaged riverine N₂O emission factors (EF₅ᵣ) of the forested, agricultural, urban and mixed watersheds were 0.066%, 0.12%, 0.95% and 0.16%, respectively, showing different deviations from the default EF₅ᵣ that released by IPCC in 2019. This points to a need for more field measurements with wider spatial coverage and finer frequency to further refine the EF₅ᵣ and to better reveal the mechanisms behind indirect N₂O emissions as influenced by watershed landscapes.

Lead (Pb) is an important pollutant and it is of significance to explore the Pb distribution, influencing factors and health risk. Pb concentration and mass load per unit area in 385 street dust samples collected from 19 cities in China were determined during 2011-2013. The results show that the Pb concentration are 68.8, 105.4, 41.7, 49.7, 75.6, 81.7, 131.9, 67.5, 109.3, 164.1, 74.8, 66.4, 99.8, 58.4, 114.0, 59.6, 103.7, 55.4 and 80.4 for Beijing, Chengdu, Daqing, Harbin, Jilin, Jinan, Kunming, Lanzhou, Luoyang, Panzhihua, Qingdao, Yinchuan, Guangzhou, Tangshan, Xi’an, Guangyuan, Nanjing, Taiyuan and Tianjin, respectively. The Pb pollution level of urban street dust varies among cities in the range of 1.72–5.56 times higher than soil background values. The allometric function can fit the change in Pb concentration with particle size well. The medium-sized (38–120 μm) particles contributed 60.2%–80.4% to the Pb load and should be highlighted when selecting street dust management techniques. Influenced by the distribution of Pb ore, the Pb concentration of urban street dust in China shows obvious regional differences, with value in the south 112% higher than that in the north. Among all kinds of mining types, metal-related mining activities discharge a large amount of Pb dust in the process of crushing and smelting, thus contributing most to the Pb load. The Pb load was also affected by transportation. The relationship between Pb load and gross domestic product (GDP) was described with the environmental Kuznets curve (EKC) model, which indicated that the Pb emissions of most cities were still increasing. Finally, the human health risk assessment model with adjusted parameters showed that the Pb risk of all cities was below the threshold. Despite all this, given the EKC law of Pb emission, long-term follow-up assessments are needed.

Land use/Land cover (LULC) associated with Cryptosporidium sp. and Giardia sp. quantification and distribution can provide identification of the environmental circulation patterns of these parasites. The aim of this research was to relate the occurrence and circulation of these parasites to the LULC watershed with poor sanitation infrastructure and livestock as important economic activity. The study involved 11 municipalities in the state of São Paulo, located in southeastern Brazil. Sampling was carried out at the catchment sites of each water supply on a monthly basis, starting in December 2014 and lasting until November 2015, totalizing 128 samples. Protozoans were quantified according to the 1623.1 US. EPA Method. For watershed delimitation, the hydrographic network was extracted from the hydrology tool of ArcGIS 10.1. The frequency of occurrence of these pathogens and the high concentrations were evidenced in the municipality with the largest urban area (16.2%) and intense livestock activity (39%) near the catchment site. The municipality that showed the lowest frequency of occurrence presented the smallest urban area (0.87%) and absence of livestock activity near the catchment site. The high concentration of pathogens suggests a correlation between the impact on water supply networks and river basin degradation caused by urban activity and livestock.

Urbanization is conducive to promoting social development and improving living standards. However, the changing land use attributed to urbanization has placed both the environment and humans at risk. Based on the long-term monitoring and the land use change during 2010–2017, we investigated the exposure of fluoride (F) and arsenic (As) in groundwater. We analyzed the temporal and spatial variation of F and As from different land use changes. The study assessed health risk for children by calculating carcinogenic risk and non-carcinogenic risk. Furthermore, we mapped the distribution pattern of F and As using GIS. For the 768 water samples collected from 2010 to 2017, F concentrations ranged between 0.10 and 5.70 mg L⁻¹ (M = 0.68 ± 0.02 mg L⁻¹), As concentrations ranged between 0.50 and 71.50 μg L⁻¹ (M = 4.28 ± 0.28 μg L⁻¹). A concerning result showed that 6.77% of F concentrations larger than 1.5 mg L⁻¹ and 11.46% of As concentrations larger than 10 μg L⁻¹ based on the recommendation by WHO, respectively. Results proved that land use change caused by human activity increased groundwater pollution and placed human health at risk. High F and As risk were found in southern Taiyuan City. In particular, the groundwater of industrial land suffered from more severe pollution, especially at the frontier of urban and suburban areas in the southern part of Taiyuan City. Land use change attributed to industrial land resulted in major increases in the F and As concentrations in groundwater across 2010–2017. Both carcinogenic risk and non-carcinogenic risk in 2016–2017 were higher than that in 2010–2015. Rational land use planning, strict groundwater protection policies and the regular monitoring of pollution levels are necessary in order to prevent the adverse health of residents.

As the most important gas-phase alkaline species, atmospheric ammonia (NH3) contributes considerably to the formation and development of fine-mode particles (PM2.5), which affect air quality and environmental health. Recent satellite-based observations suggest that the North China Plain is the largest agricultural NH3 emission source in China. However, our isotopic approach shows that the surface NH3 in the intraregional urban environment of Beijing-Tianjin-Shijiazhuang is contributed primarily by combustion-related processes (i.e., coal combustion, NH3 slip, and vehicle exhaust). Specifically, the Batch fractionation model was used to describe the partitioning of gaseous NH3 into particles and to trace the near-ground atmospheric NH3 sources. With the development of haze pollution, the dynamics of δ15N-NH4+ were generally consistent with the fractionation model. The simulated initial δ15N-NH3 values ranged from −22.6‰ to −2.1‰, suggesting the dominance of combustion-related sources for urban NH3. These emission sources contributed significantly (92% on hazy days and 67% on clean days) to the total ambient NH3 in urban cities, as indicated by a Bayesian mixing model. Based on the Batch fractionation model, we concluded the following: 1) δ15N-NH4+ can be used to model the evolution of fine-mode aerosols and 2) combustion-related sources dominate the near-ground atmospheric NH3 in urban cities. These findings highlight the need for regulatory controls on gaseous NH3 emissions transported from local and surrounding industrial sources.

As one of the most dominant ecosystems of urban green space, turfgrasses provide a wide range of ecosystem services. However, little is known about the interactions of microbial communities in turfgrass soils and how these interactions respond to expanding development of impervious surfaces during watershed urbanization. In this study, we analyzed bacterial communities and their co-occurrence patterns in turfgrass soils along an urbanization gradient as measured by the proportion of impervious surfaces in Jiulong River watershed in Fujian, China. Results show that the diversity and network size of bacterial communities negatively associated with impervious surfaces. The bacterial communities showed non-random co-occurrence patterns, with more intra-module connections observed for urbanized networks. The co-occurrence network with distinct modules of soil samples with contrasting land cover imperviousness suggested different functional organizations with altered microbial nitrogen processes. Structural equation modelling revealed that watershed impervious surfaces had indirect impacts on microbial connectivity by altering soil properties, including pH, temperature, moisture, C/N and nitrate (NO₃⁻). Moreover, impervious surfaces affected microbial connectivity far more than human population density. Our study highlights the significance of human disturbances in affecting microbial interactions and assemblies in turfgrass ecosystems through impervious surfaces and provides benefits for sustainable urban planning and management at a watershed scale.

Plastic pollution represents one of the most salient indicators of society’s impact on the environment. The microplastic component of this is ubiquitous, however, microplastic studies are seldom representative of the locations they sample. Over 12 months we explored spatiotemporal variation in microplastic prevalence across a freshwater system and in atmospheric deposition within its catchment, in one of the most temporally comprehensive studies of microplastic pollution. Microplastics were quantified in low concentrations (max 0.4 particles L⁻¹) at all freshwater sites, including upstream of urban areas, and on rivers that do not receive wastewater treatment plant effluent. Extrapolated microplastic abundances at each site varied by up to 8 orders of magnitude over the course of the sampling campaign, suggesting that microplastic surveys that do not account for temporal variability misrepresent microplastic prevalence. Whilst we do not wish to underplay the potential impacts of microplastic particles in the environment, we argue that microplastic pollution needs to be placed in a more critical context, including assessment of temporal variability, to appropriately inform legislators and consumers.