Evaluation of electromagnetic scattering characteristics of construction solid waste-A theoretical study of solid waste identification.

The surge in urban development has resulted in a substantial accumulation of construction solid waste (CSW). However, prevailing identification methods of CSW remain predominantly two-dimensional in scope and need to be more efficient. This study employs an approach, combining simulation and experimental analyses, to delve into the factors influencing the electromagnetic scattering characteristics of CSW, investigating the feasibility of employing Synthetic Aperture Radar (SAR) to recognize CSW. The findings show that the computational time of MLFMM and PO is only 3.28 % and 0.029 % of MM among different simulation methods. The results underscore the collective impact of material types, surface structures, and curvature on the scattering characteristics of CSW. The difference in average intensity between different materials can reach up to 13 dB. Exploiting these distinctions in scattering enables the precise identification of high-value waste components, such as intact bricks and steel bars, within the intricate landscape of CSW.

Global trade-driven transfer of atmospheric polycyclic aromatic hydrocarbon emissions and associated human inhalation exposure risk.

Polycyclic aromatic hydrocarbons (PAHs) are of significant public concern because of their toxicity and long-range transport potential. Extensive studies have been conducted to explore the source-receptor relationships of PAHs via atmospheric transport. However, the transfer of trade-driven regional and global PAHs is poorly understood. This study estimated the virtual PAHs emission transfer embodied in global trade from 2004 to 2014 and simulated the impact of international trade on global contamination and associated human inhalation exposure risk of PAHs. Results show that trade-driven PAHs flowed primarily from developed to less-developed regions, particularly in those regions with intensive heavy industries and transportation. As the result, international trade resulted in an increasing risk of lung cancer induced by exposure to PAHs (27.8% in China, 14.7% in India, and 11.3% in Southeast Asia). In contrast, we found decreasing risks of PAHs-induced lung cancer in Western Europe (63.2%) and the United States (45.9%) in 2004. Our findings indicate that final demand and emission intensity are the key driving factors contributing to rising and falling consumption-based PAHs emissions and related health risk respectively. The results could provide a useful reference for global collaboration in the reduction of PAHs pollution and related health risks.

Deca-BDE emissions, validation, and environmental fate in China.

Decabromodiphenyl ether (Deca-BDE) was officially listed in Annex A of the Stockholm Convention for persistent organic pollutants (POPs). It is necessary to establish its emission inventory to help reduce Deca-BDE contamination in the environment. We established a comprehensive Deca-BDE emission inventory in China. The results reveal that, from 2015 to 2017, the Deca-BDE emissions in its production source (source I) were less altered but increased annually in flame retarded plastics processing (source II), Deca-BDE-containing products usage (source III), and electronic waste (e-waste) treatment (source IV). We show that Deca-BDE emissions declined significantly in sources I and II but grew in source III and source IV from 2017 to 2018. We set up the provincial emission inventory to a gridded map on a spatial resolution of 0.25°× 0.25° latitude/longitude. The gridded inventory was incorporated into ChnMETOP model to simulate Deca-BDE concentrations in air and soil, and the modeled concentrations were compared to field-sampling data. The results show that the Deca-BDE emission inventory developed in this study agreed well with observed data, demonstrating that the Deca-BDE inventory in China developed in the present study is reliable. The inventory provides a support for quantifying human exposure risk to Deca-BDE and developing effective mitigation measures to mitigate Deca-BDE emissions.

Contamination, ecological-health risks, and sources of potentially toxic elements in road-dust sediments and soils of the largest urban riverfront scenic park in China.

Identifying the contamination and sources of potentially toxic elements (PTEs) in road-dust sediment (RDS) and the surrounding greenspace soil of urban environments and understanding their ecological-health risks are important for pollution management and public health. The contamination characteristics, ecological and probabilistic health risks, and source apportionment of eight PTEs (Cd, Pb, Cr, Cu, Ni, As, Zn, and Hg) in the Yellow River Custom Tourist Line of Lanzhou, which is the largest open urban riverfront scenic park in China, were investigated. The results showed that all the RDS PTE mean concentrations exceeded their soil background values, whereas for the surrounding greenspace soils, the concentrations of the PTEs, except for Cr and Ni, were also higher than their local background levels. Moreover, the RDS-soil system was mainly contaminated by Cd, Zn, Pb, Cu, and Hg to varying degrees, and the integrated ecological risks of PTEs in the RDS and soil were high and considerable at most sites, respectively. The probabilistic health risk assessment results demonstrated that the non-carcinogenic hazard risk for humans was negligible, but the total carcinogenic risks should be considered. Source apportionment using a positive matrix factorization model combined with multivariate statistical analyses revealed that Cr, Ni, and As in the RDS-soil system were from natural and industrial sources, Cd, Pb, Zn, Cu came from vehicle emissions and pesticide and fertilizer applications, and Hg was from natural and industrial sources and utilization of pesticides with fertilizers. This work provides scientific evidence for urban planning and human health protection in urban environments.

[Pollution Characteristics and Risk Assessment of Heavy Metals in Surface Dusts and Surrounding Green Land Soils from Yellow River Custom Tourist Line in Lanzhou].

In order to investigate the contamination levels of dust and its surrounding green land soil heavy metal pollution and potential ecological and health risks in the scenic areas of urban waterfront parks, the gardens, squares, and theme parks of the Yellow River Custom Tourist Line in Lanzhou were selected as the research area, using 27 dust samples and 26 soil samples from its surrounding green lands. The contamination characteristics and potential ecological risks of eight heavy metals (Cr, Ni, Cu, Zn, As, Cd, Hg, and Pb) were evaluated using the geo-accumulation index (Igeo), single-factor pollution index (Pi), Nemerow integrated pollution index (PN), and improved potential ecological risk index (RI). The human health risk assessment was also evaluated using the exposure risk model. The results showed that the average concentrations of the other heavy metals in the surface dusts were higher than the background values of Gansu Province and Lanzhou City, except that the As mean concentrations in the surface dusts and the surrounding green land soils were slightly lower than the Gansu Province background values. For its surrounding green land soils, the mean concentrations of the other heavy metals (Cu, Zn, Cd, Hg, and Pb) exceeded the soil background values of Gansu Province and Lanzhou City, whereas the Cr and Ni mean concentrations were lower than their corresponding soil background values of Gansu Province and Lanzhou City. The geo-accumulation and single-factor pollution indices demonstrated that a slight to moderate pollution of Cr, Cu, Zn, Cd, Hg, and Pb occurred in surface dusts, and Cu, Zn, Cd, Hg, and Pb appeared in varying degrees of contamination levels in its surrounding green land soils. The Nemerow integrated pollution index analysis manifested that the overall contamination status of the study areas was between slightly and heavily polluted. The potential ecological risk index suggested that Cd and Hg were recognized as significant pollutant elements and that the RI of the other heavy metals were all below 40, presenting slight ecological risk. The health risk assessment indicated that ingestion was the dominant exposure pathway for heavy metals from the surface dusts and the surrounding green land soils, and no carcinogenic and noncarcinogenic risks posed threats to adults and children.

[Spatial Distribution Characteristics and Source Analysis of Heavy Metals in Urban River Surface Sediments from the Lanzhou Reach of the Yellow River].

In order to investigate the contamination characteristics and potential sources of heavy metals from the urban river surface sediments in the Yellow River Basin, we selected the Lanzhou reach of the Yellow River as the object of investigation. A total of 46 surface sediment samples were collected along the Lanzhou reach of the Yellow River, and the contents of eight heavy metals, Cr, Ni, Cu, Zn, As, Cd, Hg, and Pb, were determined by using inductively coupled plasma mass spectrometry and an atomic fluorescence spectrometer. Contamination indexes including single factor pollution index (Pi) and geo-accumulation index (Igeo), together with the sediment pollution index (SPI), were used to assess heavy metal pollution characteristics and ecological risk levels in the urban river surface sediments of the Lanzhou reach of the Yellow River. Pearson's correlation analysis (CA), positive matrix factorization (PMF), and principal component analysis/absolute principal component score (PCA/APCS) were jointly employed to quantitatively analyze pollution sources of heavy metals. The results showed that the mean concentrations of the majority of heavy metals exceeded their corresponding background values of Gansu Province and Lanzhou City with the exception of As, and the spatial distribution of high concentrations of heavy metals was mainly concentrated in the corner of the river. Based on the single factor pollution and geo-accumulation indexes of the eight heavy metals, in the Lanzhou reach of the Yellow River, Cr was the dominant pollution element in the urban river surface sediments, followed by Cd and Ni. Additionally, the SPI values for the eight heavy metals in the surface sediments ranged from 0.48 to 8.56, presenting natural to low ecological risk level. Furthermore, source apportionment revealed that a mixture source of industrial and agricultural activities (77.6%) was the largest contributor of Cr, Ni, Zn, As, Cd, and Pb in the urban river surface sediments, followed by natural sources (11.4%) and a mixed source of industrial and traffic activities (11%).

Influence on the levels of PAHs and methylated PAHs in surface soil from pollution control in China: Evidence in 2019 data compared with 2005 and 2012 data.

To comprehensively clarify the pollution characteristics of persistent toxic substances, the Soil and Air Monitoring Program Phase III (SAMP-III) was conducted in 2019 in China. In total, 154 surface soil samples were collected across China, and 30 unsubstituted polycyclic aromatic hydrocarbons (U-PAHs) and 49 methylated PAHs (Me-PAHs) were analyzed in this study. The mean concentrations of total U-PAHs and Me-PAHs were 540 ± 778 and 82.0 ± 132 ng/g dw, respectively. Northeastern China and Eastern China are the two regions of concern with high PAH and BaP equivalency levels. Compared with SAMP-I (2005) and SAMP-II (2012), an obvious upward temporal trend followed by a downward trend of PAH levels was observed in the past 14 years for the first time. The mean concentrations of 16 U-PAHs were 377 ± 716, 780 ± 1010, and 419 ± 611 ng/g dw in surface soil across China for the three phases, respectively. Considering rapid economic growth and energy consumption, an increasing trend from 2005 to 2012 was expected. From 2012 to 2019, the PAH levels in soils across China decreased by 50 %, which was consistent with the decline in PAH emissions. The period of reduction of PAHs in surface soil coincided with the implementation of Air and Soil Pollution Control Actions in China after 2013 and 2016, respectively. Along with the pollution control actions in China, the pollution control of PAHs and the increase in soil quality can be expected in the near future.

Assessing the contribution of global wildfire biomass burning to BaP contamination in the Arctic.

Polycyclic aromatic hydrocarbons (PAHs) have become cause for growing concern in the Arctic ecosystems, partly due to their stable levels despite global emission reduction. Wildfire is considered one of the primary sources that influence PAH levels and trends in the Arctic, but quantitative investigations of this influence are still lacking. This study estimates the global emissions of benzo[a]pyrene (BaP), a congener of PAHs with high carcinogenicity, from forest and grassland fires from 2001 to 2020 and simulates the contributions of wildfire-induced BaP emissions from different source regions to BaP contamination in the Arctic. We find that global wildfires contributed 29.3% to annual averaging BaP concentrations in the Arctic from 2001 to 2020. Additionally, we show that wildfires contributed significantly to BaP concentrations in the Arctic after 2011, enhancing it from 10.1% in 2011 to 83.9% in 2020. Our results reveal that wildfires accounted for 94.2% and 50.8% of BaP levels in the Asian Arctic during boreal summer and autumn, respectively, and 74.2% and 14.5% in the North American Arctic for the same seasons. The source-tagging approach identified that local wildfire biomass emissions were the largest source of BaP in the Arctic, accounting for 65.7% of its concentration, followed by those of Northern Asia (17.8%) and Northern North America (13.7%). Our findings anticipate wildfires to play a larger role in Arctic PAH contaminations alongside continually decreasing anthropogenic emissions and climate warming in the future.

New emission inventory reveals termination of global dioxin declining trend.

Accurate estimates of spatiotemporally resolved Polychlorinated dibenzo-p-dioxins (PCDD/Fs, or dioxins) emissions are critical for understanding their environmental fate and associated health risks. In this study, by utilizing an empirical regression model for PCDD/Fs emissions, we developed a global emission inventory for 17 toxic PCDD/Fs congeners from 8 source sectors with a spatial resolution of 1° × 1° from 2002 to 2018. The results show that PCDD/Fs emissions decreased by 25.7 % (12.5 kg TEQ) between 2002 and 2018, mostly occurring in upper- and lower-middle income countries. Globally, open-burning processes, waste incineration, ferrous and nonferrous metal production sectors and heat and power generation were the major source sectors of PCDD/Fs. Spatially, high PCDD/Fs emissions were mainly identified in East and South Asia, Southeast Asia, and part of Sub-Saharan Africa. We find that the declining trend of dioxin emissions over the past decades terminated from the early 2010s due to increasing significance of wildfire induced emissions in the total emission. The PCDD/Fs emission inventory developed in the present study was verified by inputting the inventory as initial conditions into an atmospheric transport model, the Canadian Model for Environmental Transport of Organochlorine Pesticides (CanMETOP), to simulate PCDD/Fs concentrations in air and soil. The predicted concentrations were compared to field sampling data. The good agreement between the modeled and measured concentrations demonstrates the reliability of the inventory.

Signatures of Indian endosulfan usage in China's environment.

Endosulfan, as an organochlorine pesticide (OCPs), was widely used in agriculture. As the largest endosulfan user country in the world and adjacent to China, it is interesting to know to what extent the endosulfan usage of India could affect the environment in China. In this study, we established gridded endosulfan usage, atmospheric emission, and soil residue inventories in 2010 based on its application in different crops in China and India. We employed an atmospheric transport model CanMETOP to simulate atmospheric and soil concentrations, as well as dry and wet deposition flux of α- and ß-endosulfan. Results were used to assess the signatures of Indian endosulfan usage in the China's environment. In 2010, endosulfan usage, atmospheric emissions, and highest soil residue in China were 3083.9, 1312.7, and 587.5 tonnes, and 3204.8, 1441.4, and 463.7 tonnes in India, respectively. The spatial distribution of modeled atmospheric and soil concentrations, and dry deposition fluxes of endosulfan were in line with its usage but wet deposition fluxes were mainly identified in Southern China and Sichuan basin with heavy rainfall, especially for α-endosulfan. Endosulfan tended to transport from India to Tibetan plateau, Yunnan-Kweichow Plateau, and some provinces in southern China under the Indian Summer Monsoon regime. Due to its stronger volatility, α-endosulfan posed a more significant impact on China's environment via the atmospheric transport from India compared to ß-endosulfan. Although rainfall during Indian Summer Monsoon reduced endosulfan levels in the air during its journey from India to China, it was observed that Indian endosulfan usage in 2010 contributed more than 50% of atmospheric concentrations and 30% of soil concentrations of α-endosulfan in some regions in Tibetan plateau.

Assessing Safety of Market-Sold Fresh Fish: Tracking Fish Origins and Toxic Chemical Origins.

Increasing global and domestic food trade and required logistics create uncertainties in food safety inspection due to uncertainties in food origins and extensive trade activities. Modern blockchain techniques have been developed to inform consumers of food origins but do not provide food safety information in many cases. A novel food safety tracking and modeling framework for quantifying toxic chemical levels in the food and the food origins was developed. By integrating chemicals' multimedia environment exchange, food web, and source tracking systems, the framework was implemented to identify short-chain chlorinated paraffin (SCCP) contamination of fresh hairtail fish sold by a Walmart supermarket in Xi'an, northwestern China, and sourced in Eastern China Sea coastal waters. The framework was shown to successfully predict SCCP level with a mean of 17.8 ng g-1 in Walmart-sold hairtails, which was comparable to lab-analyzed 21.9 ng g-1 in Walmart-sold hairtails. The framework provides an alternative and cost-effective approach for safe food inspection compared to traditional food safety inspection techniques. These encouraging results suggest that the approach and rationale reported here could add additional information to the food origin tracking system to enhance transparency and consumers' confidence in the traded food they consumed.

Effects of African BaP emission from wildfire biomass burning on regional and global environment and human health.

The vegetation burning caused by wildfires can release significant quantities of aerosols and toxic chemicals into the atmosphere and result in health risk. Among these emitted pollutants, Benzo(a)pyrene (BaP), the most toxic congener of 16 parent PAHs (polycyclic aromatic hydrocarbons), has received widespread concerns because of its carcinogenicity to human health. Efforts have been made to investigate the environmental and health consequences of wildfire-induced BaP emissions in Africa. Still, uncertainties remain due to knowledge and data gaps in wildfire incidences and biomass burning emissions. Based on a newly-developed BaP emission inventory, the present study assesses quantitatively the BaP environment cycling in Africa and its effects on other continents from 2001 to 2014. The new inventory reveals the increasing contribution of BaP emission from African wildfires to the global total primarily from anthropogenic sources, accounting for 48% since the 2000 s. We identify significantly higher BaP emissions and concentrations across sub-Saharan Africa, where the annual averaged BaP concentrations were as high as 5-8 ng/m3. The modeled BaP concentrations were implemented to estimate the lifetime cancer risk (LCR) from the inhalation exposure to BaP concentrations. The results reveal that the LCR values in many African countries exceeded the acceptable risk level at 1 × 10-6, some of which suffer from very high exposure risk with the LCR>1 × 10-4. We show that the African BaP emission from wildfires contributed, to some extent, BaP contamination to Europe as well as other regions, depending on source proximity and atmospheric pathways under favorable atmospheric circulation patterns.

Gridded emission inventory of organophosphorus flame retardants in China and inventory validation.

The bioaccumulation and adverse effects of organophosphorus flame retardants (OPFRs) on human health have become a global concern. China produces the largest amount of OPFRs globally and has the highest global market share. However, little is known about its emission level and environmental cycling, thereby causing uncertainties in the assessment of the environmental and health impacts of OPFRs. We developed a gridded annual OPFRs emission inventory at 1/4° longitude by 1/4° latitude resolution over China from 2014 to 2018. The results show that the annual OPFRs emissions increased from approximately 670 tons/yr in 2014 to 1000 tons/yr in 2018 in China. Higher OPFR emissions were identified in Jiangxi, Shandong, Beijing-Tianjin-Hebei (BTH), Yangtze River Delta (YRD), and Pearl River Delta (PRD). In total, 2400 tons of OPFRs were released into the atmosphere during the multi-year period, in which production accounting for 56.6% of total OPFR emissions in China. An atmospheric transport model, the Canadian Model for Environmental Transport of Organochlorine Pesticides (CanMETOP), was employed to verify the gridded emission inventory and elucidate the atmospheric environmental fate of OPFRs. Modeled OPFRs in the air and soil agreed reasonably well with observed data, suggesting that the developed inventory was, to a large extent, reliable. The modeled atmospheric and surface soil concentrations of OPFRs across China ranged from 0 to 119 ng/m3 and 0 to 428 ng/g, respectively. East China is subjected to more intense OPFR contamination than the rest of the country. The results provide a valuable dataset and assessment of OPFRs, which may aid policy-makers and the scientific community in developing emission control strategies and evaluating the health and environmental consequences of OPFRs in China.

The atmospheric lead emission, deposition, and environmental inequality driven by interprovincial trade in China.

Lead (Pb) as a hazardous air pollutant has raised widespread concerns due to its adverse and toxic effects on the ecological environment and human health. Here we integrated the multi-regional input-output (MRIO) model and an atmospheric transport model to examine regional environmental inequality (REI) index induced by Pb emission transfers, and to evaluate the impacts of interprovincial trade on regional atmospheric Pb concentrations and dry deposition fluxes in China in 2012. In 2012, approximately 57.4% ~ 72.6% of Pb emissions in well-developed eastern regions (Beijing-Tianjin, Yangtze River Delta (YRD)) and the southern seaboard of China were embodied in other regions in China subject to the demands from these well-developed regions to industrial products and services. Our results, based on the net virtual flows of Pb emission and value-added, indicate that most provinces in the eastern seaboard of China outsource Pb emission and benefit from the interprovincial trade by reducing their Pb emissions. REI indexes show that the well-developed Guangdong province outsources its Pb emission but has low economic gains. Many less-developed provinces in central China enhance virtual Pb emission inflow but have high economic gains. Whereas, inland provinces in western China not only experience Pb emission increase, but also suffer from indirect economic loss due to trade with well-developed provinces to meet their increasing demands to Pb emission abundant industrial products from these provinces in eastern China which are mostly provided by less-developed but energy and mineral product abundant provinces in western China. For example, the province pair with highest REI index was Jiangsu-Inner Mongolia (REI = 2.47), which revealed that Jiangsu was the largest beneficiary which exported 37.2 t of net Pb emission and gained value-added of 521.4 billion RMB through trade with Inner Mongolia which suffered from both virtual Pb inflow and economic loss in 2012. As a result of interprovincial trade, Pb dry deposition in central and eastern China was decreased but increased in western China. Overall, interprovincial trade reduced 17.6% of atmospheric Pb dry deposition in China.

[Gridded Emission Inventories of Major Criteria Air Pollutants and Source Contributions in Lan-Bai Metropolitan Area, Northwest China].

Lan-Bai Metropolitan Area in Gansu province is an important heavy-industry base with the highest level of total air pollutant emissions in Northwest China. It is significant to study the high-resolution pollutant emission inventory to forecast regional air quality and to simulate pollutant emission reduction, as well as provide early warnings and forecasts, and to control air pollution. Taking Lanzhou and Baiyin as the main research areas, this study established the gridded emission inventories of seven major criteria air pollutants in the Lan-Bai Metropolitan Area based on emission data and statistical yearbooks of 2015-2016. The spatial pollution characteristics and emission source contributions were also studied. The results showed that the total annual emissions of seven major criteria air pollutants in the Lan-Bai Metropolitan Area were as followings:NOx 2.22×105 t, NH3 4.53×104t, VOCs 7.74×104t, CO 5.62×105 t, PM10 4.95×105 t, PM2.5 1.91×105 t, and SO2 1.37×105 t. Among them, annual CO emissions were the highest, while the annual emissions of NH3 were the lowest. The comparison of this gridded emission inventories with the Peking and Tsinghua University's MEIC inventories, found that the consistency of the three inventories for traffic source was relatively high, but for the total emissions and industrial source emissions of CO, a 30%-40% difference was found when compared with emissions in the Peking and Tsinghua University's inventories. The main differences were from the collected emission factors and the different resolution and years for collected data. The industrial non-combustion process sources, accounting for the largest proportion, were mainly concentrated in urban areas for the other six major criteria air pollutants except for NH3. The main contributing sources of NH3 were from the use of nitrogen fertilizers and livestock emissions, so its spatial pollution distribution was mainly affected by farmland distribution and other factors. It can be concluded that countermeasures, such as controlling industrial non-combustion process sources, integrating high-quality and high-efficiency power supply, using clean energy, strict dust emission control on construction sites and industrial production facilities, as well as urban greening could effectively reduce the emissions of six major criteria air pollutants including NOx, VOCs, CO, PM10, PM2.5, and SO2 in the Lan-Bai Metropolitan Area. The reduction of NH3 emission mainly depends on reducing the use of nitrogen fertilizer and controlling livestock emissions in the rural regions of Lan-Bai Metropolitan Area. This paper also used Monte Carlo uncertainty analysis to evaluate uncertainty in the gridded emission inventories, in which the maximum uncertainty was -31%-30% for NH3, the uncertainty of CO at -18%-16% was minimal. Therefore, the overall credibility was high for the established gridded emission inventories in this study.

[Sources and Health Risks of Atmospheric Polychlorinated Biphenyls in an Urban/Industrial Areas, Northwest China].

A passive air sampler was used to monitor the concentration and contamination profile of 18 polychlorinated biphenyls (PCBs) in the atmosphere over the urban and industrial area of Gaolan, a city in northwest China, during the non-heating and heating seasons of 2018, and the sources, pollutant transport, and the health risks of PCB exposure were analyzed and assessed using principle component analysis, trajectory modeling, and inhalation exposure modeling. The atmospheric concentration in the study area ranged from 110.2 to 429.9 pg·m-3, and the highest average concentration was found at the industrial estate. Tetra-PCBs and penta-PCBs were the dominant homologue groups, and the percentage of tetra-PCBs increased in the heating season. Combustion and industrial thermal processes, PCB-containing electrical equipment, and the combined source of volatilization from paint, combustion, and industrial thermal processes were considered to be the main sources, and the source of combustion and industrial thermal processes contributed the largest proportion of PCBs at 40.8%. Largely, the emission of UP-PCBs would significantly influence PCB pollution in the study area. Trajectory analysis results illustrated that PCBs emitted from sources in the study area would be transmitted to Lanzhou City atmospherically; local pollution would be the main source of PCBs contamination in the study area during the non-heating season, while the atmospheric input of PCBs transmitted from the northwest region would be another source during the heating season. Health risk analysis showed that the non-cancer risk of PCBs exposure was low in all age groups; however, lifetime cancer risks exceeded 10-6. PCBs emitted from combustion and industrial thermal processes sources would have a strong impact on resident exposure to PCBs, and adverse health effects would be caused due to long-term inhalation exposure of the inhabitants to PCBs contamination in the study area.

Multiple exposure pathways of first-year university students to heavy metals in China: Serum sampling and atmospheric modeling.

In this study, we collected 308 serum samples from 17 to 20 year old first-year university students who were recruited from Lanzhou University in China a few days after their enrollment to measure the serum Pb, Cd, Hg, and As levels, and specific questionnaires for age, sex, settlement and dietary structure were designed. A 3-D atmospheric transport model was used to simulate the atmospheric concentration and dry deposition across China based on gridded Pb emission inventory to examine the association between the spatial distribution of serum concentrations and environmental fates of Pb. The mean serum Pb, Cd, Hg, and As concentrations averaged over all participating young students were 21.38, 1.46, 3.86, and 4.69 µg/L, respectively. The Pb, Cd, and Hg levels in 3%, 7%, and 20% serum samples exceeded the standards. The minimum serum As and Hg concentrations and the maximum serum Pb and Cd concentrations occurred in urban areas. Seafood diet habits (P < 0.05), sex (P < 0.05), and relocation (P < 0.01) caused significant differences in serum As, Pb, and Cd concentrations. A cluster analysis was carried out to classify the exposure pathways for target contaminants. The results indicated that 4 heavy metals in the serum of volunteers from northern China could be grouped into the same category, in which significant positive correlations were found between the serum heavy metal levels and background concentrations of surface soil. However, in other provinces and metropolises, the atmospheric pollution level played a critical role involving in the inhalation exposure pathway. We demonstrated that serum Pb levels in freshman students were related to the atmospheric transport and dry deposition of Pb.

WRF-Chem simulations of ozone pollution and control strategy in petrochemical industrialized and heavily polluted Lanzhou City, Northwestern China.

As the largest petrochemical industrialized city in northwestern China since the 1950s, Lanzhou has been well-known for its heavy surface ozone pollution. Given abundant emission sources of ozone precursors and the favorable environmental conditions for O3 formation, this study performed extensive atmospheric chemistry modeling investigations subject to 11 emission control scenarios. These scenarios increased and decreased emission levels of total volatile organic compound (TVOC) and nitrogen oxides (NOx), the two surface ozone (O3) precursor gases, to examine the relationships between O3 and NOx and TVOC. The modeling investigation was carried out for the summer of 2016 in the downtown and petrochemical industrial suburb in the city of Lanzhou. The results revealed that surface O3 in the downtown area of Lanzhou was controlled by VOCs and in the petrochemical-industrialized western suburb by NOx. Higher ozone levels were simulated in the west suburb of the city as compared with the downtown area, agreeing with measured data. The relationships between modeled TVOC/NOx ratios and O3 reductions, as well as the titration effect, were also discussed. The model results provided useful references for the mitigation strategy of ozone reduction in Lanzhou and other major cities in northwest China with similar climate and topography conditions.

[Atmospheric Pollution Characteristics and Inhalation Exposure Risk of Nitrated Polycyclic Aromatic Hydrocarbons in PM2.5 at the Ningdong Energy and Chemical Industry Base, Northwest China].

Atmospheric PM2.5 samples were collected by using the active sampling method to investigate the pollution characteristics of nitrated polycyclic aromatic hydrocarbons (NPAHs) at the Ningdong Energy and Chemical Industry Base, Northwest China. Furthermore, the primary sources and the contributions of secondary formation sources as well as the inhalation exposure risks were identified. The main results were as follows. The concentration levels of ∑12NPAHs in PM2.5 ranged from 2.06 ng·m-3 to 37.14 ng·m-3 at the Ningdong Energy and Chemical Industry Base. The average concentrations of ∑12NPAHs were (25.57±5.76) ng·m-3 in winter and (6.22±1.74) ng·m-3 in summer for the Baofeng sampling site associated with the energy industry. The average concentrations of ∑12NPAHs were (7.13±1.44) ng·m-3 in winter and (2.58±0.39) ng·m-3 in summer for the Yinglite sampling site associated with chemical and electricity industries. The levels of ∑12NPAHs in PM2.5 were higher in winter than those in summer because of the increased heating in winter. Atmospheric pollution levels of NPAHs at the Baofeng sampling site were generally higher than those at the Yinglite sampling because of the higher primary NPAHs emissions from coal mining and coke production in Baofeng compared with those from the chemical industry in Yinglite. The calculated nocturnal/diurnal ratios revealed that the concentrations of ∑12NPAHs in PM2.5 during the summer season were higher in the daytime than those in the nighttime, but the opposite trend occurred in winter, thus indicating that secondary formation processes made more contributions to NPAHs during summer in the daytime. The congener profiles of NPAHs were mainly composed of primary emission markers such as 2-nitrofluorene (2N-FLO) and 6-nitrochrysene (6N-CHR), which were the predominant ones in winter and summer for both the Baofeng and Yinglite sampling sites. Total proportions of 2N-FLO and 6N-CHR were 46% in winter and 73% in summer for Baofeng and 59% in winter and 55% in summer for Yinglite, respectively. Meanwhile, 3N-PHE, which is a marker compound of secondary formation processes, accounted for a higher percentage in summer especially at Yinglite. This finding revealed that the chemical production at Yinglite was associated with higher precursor emissions than that of Baofeng, and thus, more NPAHs were derived from secondary formation processes. Moreover, ∑12NPAHs/∑16PAHs ratios were calculated to identify the potential sources of NPAHs across the city. The results indicated that higher environmental temperatures in summer promoted the degradation of PAHs and secondary formation of NPAHs, and thus, secondary formation contributed more to NPAHs in summer than in winter. Furthermore, lung cancer risks induced by inhalation exposures to ∑5NPAHs were assessed based on the BaP equivalent toxicity factor. The results showed that the lung cancer risk values of ∑5NPAHs were (3.06×10-5±1.36×10-5) in winter and (1.79×10-5±0.80×10-5) in summer for the Baofeng sampling site, while the risk values were (2.85×10-5±1.20×10-5) in winter and (1.86×10-5±0.83×10-5) in summer for the Yinglite sampling site. Notably, the lung cancer risk values in our study for both sampling sites were higher than the standard limit value (1.00×10-5) of the California Environmental Protection Agency, which indicates that the local population at the Ningdong Energy and Chemical Industry Base has been subjected to potentially elevated lung cancer risks due to inhalation exposures to PM2.5-bound NPAHs.

[Pollution Characteristics and Occupational Exposure Risk of Heavy Metals in Indoor and Outdoor Ambient Particles at a Scaled Electronic Waste Dismantling Plant, Northwest China].

Atmospheric particle samples (PM1.0、PM2.5、PM10) were collected from three sampling sites (indoor and outdoor workplaces of a formal e-waste dismantling plant, and upwind area) in an arid area of Northwest China. The contents of six heavy metals (Cd, Cr, Cu, Ni, Pb, and Zn) were analyzed using ICP-OES. Based on this data, the concentration levels, size distribution characteristics, and occupational exposure risks of heavy metals at the indoor and outdoor dismantling workplaces were studied. Particle analysis showed that Zn (4890 ng·m-3 indoors, 1245 ng·m-3 outdoors)、Pb (indoors 1201 ng·m-3, outdoors 240 ng·m-3), and Cu (indoors 1200 ng·m-3, outdoors 110 ng·m-3) showed higher pollution levels indoors and outdoors at the dismantling workplace. Moreover, the indoor concentration was much higher than that outdoors, indicating that the dismantling activity was the main cause of the high levels of heavy metal contamination. The indoor and outdoor air pollution characteristics were closely related to the types of electronic waste dismantled. Occupational exposure risk assessments showed that the total non-carcinogenic hazard quotient (HQ) of the indoor and outdoor dismantling workshops was 1.62×10-3, and 3.60×10-4, respectively, and the carcinogenic risk values were 2.69×10-7 and 2.59×10-9. Cd caused the greatest carcinogenic and non-carcinogenic risks at both indoor and outdoor dismantling workplaces, but it was still far below the limits (1.0) and acceptable ranges (1×10-6) stipulated by U.S. EPA, indicating that the health risks caused by heavy metals were minor or negligible. Heavy metals in the ambient particulate matter released from an adequately equipped and formally managed e-waste dismantling plant would not lead to any public health risk. The sedimentation characteristics of particulate heavy metals in different organs of the human respiratory system exhibited that the smaller the particle size was, the greater the proportion of deposition in the depths of the respiratory system was. Enterprises should make scientific and effective decisions on the respiratory health risks caused by such fine particles to the health of professional workers.