Little is known about fine particulate matter (PM2.5) exposure among pregnant women in rural China. This study aims to characterize exposure to PM2.5 among pregnant women in rural China, and investigate potential risk factors of personal exposure to PM2.5. The data were obtained from a birth cohort study that enrolled 606 pregnant women in Xuanwei, a county known for its high rates of lung cancer. The personal exposure to PM2.5 was measured using small portable particulate monitors during each trimester of pregnancy. Participants were interviewed using structured questionnaires that sought information on risk factors of PM2.5 exposure. The daily exposure to PM2.5 among the pregnant women ranged from 19.68 to 97.08 μg/m3 (median = 26.08). Exposure to PM2.5 was higher in winter and autumn than other seasons (p < 0.05); higher during the day than during the night (p < 0.001); and greater during cooking hours than during the rest of the day (p < 0.001). Using a mixed effects model, domestic solid fuel for cooking (β = 1.75, p < 0.001), winter and autumn (β = 2.96, p < 0.001), cooking ≥ once per day (β = 1.58, p < 0.05), heating with coal (β = 1.69, p < 0.001), secondhand smoke exposure (β = 1.59, p < 0.001) and township 1(β = 2.39, p < 0.001) were identified as risk factors for personal exposure to PM2.5 of pregnant women throughout pregnancy. Indirect effects of season and township factors on personal PM2.5 exposure were mediated by heating, cooking and domestic fuel using. In conclusion, PM2.5 levels in Xuanwei exceeded WHO guidelines. Seasonal and township factors and individual behaviors like domestic solid fuel using for cooking, heating with coal and secondhand smoke exposure are associated with higher personal PM2.5 exposure among pregnant women in rural China.

The Haihe River Basin is a polluted area affected by the developing industry and intensive agricultural activities in China. Dissolved organic matter (DOC) and light-absorbing characteristics of chromophoric dissolved organic matter (CDOM) were monitored in different tributaries of China within the Haihe River basin during spring and autumn. The concentration of DOC during spring was higher than during autumn (p < 0.01), and the evaporation was an important factor affecting the concentration of DOC in the basin. By contrast, the proportion of inputs due to terrigenous plants during autumn was higher than during spring. Carbon stable isotope analysis δ¹³C and C: N ratio of DOC, evidenced the inputs of DOC in the Haihe River basin from different sources including sewage, terrestrial plants, soil, and plankton. Isotopic analysis of δ¹³C and excitation-emission matrix (EEM) with fluorescence regional integration (FRI) analysis supported the hypothesis that allochthonous inputs contributed substantially to the inputs of DOC in the Haihe River basin, coming largely from sewage (9.8%–81.2%) and terrestrial plants (13.3%–65.8%). Depending on the source of DOC and contribution, four types with different EEM spectra were set. Type I, river water from sewage (81.2%); Type II, river water with input from terrestrial plants (65.8%); Type III, river water with plankton (36.4%), and Type IV, river water with soil-derived DOC (33.9%). The results demonstrated that the combined methodology using ¹³C stable isotope and EEM-FRI can be used to characterize the components of DOC in river waters. This approach was important for tracking the concentration and composition of DOC in river waters from different input sources and for better understanding concerning the local regulation of the terrestrial carbon cycle.

Accumulation of potentially toxic elements (PTEs) in agricultural soils has become an increasingly global issue driven by industrialization. A credible knowledge of their distribution and diverse sources in soils is essential to developing effective measures of identifying accumulation of PTEs in rural and periurban environments. However, the assessment of PTE pollution levels and discrimination of anthropogenic and natural sources remain a serious challenge. In China, most studies are focused on highly industrialized and/or urbanized regions, while limited attention has been given to agricultural areas where diffuse source contamination prevails. Therefore, a large dataset of 5207 surface soil samples (1 × 1 km) and 1311 subsoil samples (2 × 2 km) were collected from an agriculturally dominated region in eastern China. Soil total concentrations of As, Cd, Cr, Cu, Hg, Ni, Pb and Zn were analyzed along with additional edaphic variables relevant to PTE accumulation in soils (e.g., pH, SOC). Concentrations of Cr, Ni, Pb and Zn for all sites were lower than those of the risk-screening values. However, elevated concentrations of Cd and Hg observed in surface soils were associated with anthropogenic activities. Land use pattern had a significant impact on the spatial variation of PTEs. Elevated levels of Cd were uniquely associated with high phosphorus and soil organic matter (SOM) contents, and elevated Hg was associated with coal-fired power plants and historical application of fertilizer and Hg-containing pesticides. The data presented herein indicated that geogenic process likely caused a net depletion of As, Cr, Cu, Ni, Pb and Zn in topsoil, despite surface deposition from anthropogenic sources. The result of this study revealed that using subsoil concentrations of PTEs to establish background or reference concentrations might lead to an erroneous assessment of pollution levels in surface soils.

Early-life exposure to toxicants may have lasting effects that adversely impact later development. Thus, although the production and use of a toxicant have been banned, the risk to previously exposed individuals may continue. BDE-47, a component of commercial penta-BDEs, is a persistent organic pollutant with demonstrated neurotoxicity. To investigate the persistent effects of BDE-47 and the mechanisms thereof, we employed a metabolomics approach to analyze the brain, blood and urine of mice exposed to BDE-47 for 28 days and then 3 months post-exposure. In the brain, BDE-47 was detectable just after exposure but was below the limit of detection (LOD) 3 months later. However, the metabolomic alterations caused by early-life exposure to BDE-47 persisted. Potential biomarkers related to these alterations included phosphatidylcholine, lysophosphatidylcholine, sphingomyelin and several amino acids and biogenic amines. The metabolic pathways involved in the response to BDE-47 in the brain were mainly those related to glycerophospholipid metabolism, sphingomyelin metabolism and neurotransmitter regulation. Thus, our study demonstrates the utility of metabolomics, as the omics most closely reflecting the phenotype, in exploring the mechanisms underlying the lasting effects induced by early-life BDE-47 exposure.

Present study aims to examine the efficiency of co-vermicomposting amended with activated sludge and E. fetida earthworm for bioremediation of diesel and gasoline from contaminated soil. The diesel and gasoline removal efficiency and degradation rates coefficients were estimated with gas chromatography (GC) analysis and first-order kinetics. The removal of gasoline and diesel in different co-vermicomposting processes with and without E. fetida ranged between 65-100% and 24.94–63.93%, respectively within 90- day experiment. Removal of gasoline and diesel increased in soil with addition of earthworm (E. fetida); higher degradation rate coefficients (k) were observed for co-vermicomposting with earthworm compared with co-vermicomposting processes. The highest k (0.014) for diesel degradation was estimated for microcosm reactor 4 (R4), where high numbers of E. fetida accelerate the less biodegradable organic contaminant from the soil matrices. The reasonable survival rates of earthworms in exposure to high concentration of petroleum-derivatives contaminated soils indicated increased activity of ligninolytic diesel–degrading earthworms and microorganisms. Therefore, co-vermicomposting amended with activated sludge is suggested as feasible and promising technologies for bioremediation of high content of organic contaminants from the soil matrices.

In this study, the degradation of eight bromophenols (BPs), including monobromophenols (2-BP, 3-BP, and 4-BP), dibromophenols (2,4-DBP, 2,6-DBP, and 3,5-DBP), a tribromophenol (2,4,6-TBP) and a pentabromophenol (PBP), by a Fe(VI) reaction process at a pH of 8.0 was systematically studied. It was concluded that their degradation rates increased with increasing Fe(VI) concentrations in solution. The removal of 2,4,6-TBP, 2-BP, and 2,6-DBP was faster than that of the other five BPs, which could be attributed to the position of the substituting Br atom. Moreover, the direct oxidation and coupling reactions greatly influenced the reactivity of the bromophenols with Fe(VI). The electron paramagnetic resonance (EPR) analysis confirmed the presence of hydroxyl radicals in present system. The oxidation reaction products of PBP and 2-BP were recognized by an electrospray time-of-flight mass spectrometer; hydroxylation, hydroxyl substitution, the cleavage of the C–C bond, direct oxidation and polymerization via an end linking mechanism were noticeably found in the reaction process, resulting in the formation of polymerization products and causing hydroxylation to occur. Theoretical calculations further determined the possible oxidation sites of 2-BP and PBP. This study may provide comprehensive and important information on the remediation of BPs by Fe(VI).

Coral reefs worldwide are degrading at alarming rates due to local and global stressors. There are ongoing needs for bioindicator systems that can be used to assess reef health status, the potential for recovery following destructive events such as tropical storms, and for the success of coral transplants. Benthic foraminiferal shells are ubiquitous components of carbonate sediment in reef environments that can be sampled at minimal cost and environmental impact. Here we review the development and application of the FoRAM Index (FI), which provides a bioindicator metric for water quality that supports reef accretion. We outline the strengths and limitations of the FI, and propose how it can be applied more effectively across different geographical regions.

Microplastics (MPs, plastics < 5 mm) are a growing concern in ecosystems, being found in the soil and water environment. One of the primary sources of MPs has been suspected to be road dust in urban areas as it can flow into waters with runoff. To understand the occurrence of MPs (100 μm–5 mm) in surface road dust of three cities (Kusatsu, Shiga, Japan; Da Nang, Vietnam; and Kathmandu, Nepal), we collected surface road dust samples. The samples were pretreated (organic matter decomposition and gravity separation), and all MP candidates were individually observed by microscope for color, shape, and size; and analyzed their polymer types using fourier transform infrared spectrometry. The abundances of MPs 100 μm to 5 mm in size were 2.0 ± 1.6 pieces/m2 (13 polymer types) in Kusatsu, 19.7 ± 13.7 pieces/m2 in Da Nang (14 types), and 12.5 ± 10.1 pieces/m2 in Kathmandu (15 types). We classified the MPs into two groups; containers/packaging-MPs and rubber-MPs. Among all MPs, the containers/packaging-MPs accounted for 55 ± 5% of the polymer types composition. In contrast, the rubber-MPs accounted for 16 ± 6% of all MPs which were higher than those previously published for environmental water and sediment samples. The containers/packaging-MPs were fragments of various colors while most of the rubber-MPs were fragments or granules in black. The number–size distributions of MPs showed that the mode of formation explains the differences between their polymer types (tearing for containers/packaging-MPs and abrasion for rubber-MPs). In Da Nang and Kathmandu, the abundance of containers/packaging-MPs and rubber-MPs were correlated so that those MPs might be micronized from the originated materials in the sources with the similar composition (e.g. dump points). It was indicated that the characteristics of MPs pollution in surface road dust might be different depending on waste management practices.

Summertime ozone (O₃) concentrations over China continue to increase although the governmental Clear Air Actions have been carried out since 2013. The worst O₃ pollution is confronted over North China Plain. Ozone polluted days (with observed regionally-averaged maximum daily 8-h average (MDA8) O₃ concentrations exceeding 80 ppbv) in May–July in North China increased from 35 days in year 2014 to 56 days in year 2018, and persistent O₃ pollution episodes that lasted for 5 days or longer (OPEs5) contributed 14.3% and 66.1% to those O₃ polluted days in 2014 and 2018, respectively. Model simulations suggest that O₃ transport from central eastern China (including Shandong, Henan, Jiangsu and Anhui Provinces) contributes 36% of the enhanced O₃ concentrations in North China during OPEs5 relative to the seasonal mean. We find that emission control of volatile organic compounds in central eastern China is most effective to alleviate intensity of OPEs5 in North China.

As inland freshwaters act as a major transport pathway for marine microplastic pollution, microplastic pollution in freshwater systems has recently received growing attention. However, the role of environmental and spatial factors in shaping the distribution and characteristics of microplastic pollution in reservoir ecosystems is not well understood. Here, we studied microplastic pollution in the surface water of the Yulin River, a typical tributary of the upper reaches of the Three Gorges Reservoir (TGR). The abundance of microplastics were 1.30 × 10⁻², 1.95 × 10⁻¹ and 3.60 × 10⁻¹ items/L in the mainstream, tributaries and bays of the Yulin River, respectively. Polyethylene, polypropylene, and polystyrene were identified as the predominant types. The most common shapes were line/fiber and foam. Small-sized particles dominated the collected microplastics. Aged surface was identified by scanning electron microscopy and X-ray photoelectron spectroscopy. The microplastics in the Yulin River were largely of secondary origin. Microplastic pollution varied in space. The abundance of microplastic was higher upstream reaches than downstream, which was correlated with anthropogenic activity. The backwater of the TGR increased the abundance of microplastic in the estuary of the Yulin River. The abundance of microplastic was negatively correlated with the channel width. This study is helpful for understanding the characterics and distribution of microplastics in reservoir ecosystems within underdeveloped area, and can thereby inform well-directed strategies to mitigate microplastic pollution.