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Water eutrophication caused by nitrogen pollution is an urgent global issue that requires attention. The Qingyi River is a typical micro-polluted river in China. In this study, we took this river as the research object to investigate the nitrogen pollution purification capacity of a herbaceous plant, Rumex japonicus Houtt. (RJH). Compared to nitrate nitrogen (NO 3 −-N) and nitrite nitrogen (NO 2 −-N), RJH showed better purification performance on total nitrogen (TN), total phosphorus (TP) and ammonia nitrogen (NH 4 +-N), with a highest removal rate of 37.22%, 52.13%, and 100%, respectively. RJH could completely remove ammonia nitrogen and exhibit excellent resistance to pollutant interference when the initial concentration of ammonia nitrogen in the cultivation devices increased from 1 mg/L to 10 mg/L or in the actual river. This indicated the great application potential of RJH in ammonia nitrogen removal from natural micro-polluted rivers. In addition, combined effects of nitrification of roots, absorption of self-growth, stripping, and others contributed to nitrogen removal by RJH. Particularly, the nitrification of roots played a dominant role, accounting for 73.85% ± 8.79%. High-throughput sequencing results indicate that nitrifying bacteria accounted for over 75% of all bacterial species in RJH. Furthermore, RJH showed good growth status and strong adaptability. The correlation coefficients of its relative growth rate with chlorophyll A and the degradation rate of absorption were 0.9677 and 0.9594, respectively. Our research demonstrates that RJH is one of the excellent varieties for ammonia removal. This provides a very promising and sustainable method for purifying micro-polluted rivers. [Display omitted] • A Rumex japonicus Houtt.(RJH)-based phytoremediation technology was proposed. • Nitrification, absorption, stripping and other effects influenced ammonia removal. • Nitrification of roots accounted for 73.85% ± 8.79% of the total degradation rate. • The good growth status and strong purification ability of RJH were verified. [ABSTRACT FROM AUTHOR]

Thus far, the effect of environmental antibiotics exposure to offspring's growth remains unclear. Here we aimed to evaluate whether and to what extent environmental antibiotics exposure is associated with fetal and postnatal growth. A total of 735 pregnant women and their full-term offspring from the Shanghai Obesity Birth Cohort were involved in the study. Maternal urine specimen was collected during the third trimester, and urinary concentration of fifteen environmental antibiotics was measured by liquid chromatography-tandem mass spectrometry and enzymatic method. Children were followed at birth, 12, 24 and 60 months, and growth parameters of the weight and height of children were recorded. Linear regression model was applied, and it was found that maternal veterinary antibiotic (VA) concentration was negatively associated with birth weight and ponderal index [per natural-logarithm (ln)-unit: adjusted β (95% confidence interval, CI) = – 42.1 (– 74.0, – 10.3) for birth weight, –0.11 (– 0.19, – 0.02) for birth weight z-score, and – 0.03 (– 0.05, – 0.002) for ponderal index]. Regarding specific VA, each ln-unit increment of florfenicol concentrations was likely to be associate with 39.7 g (95%CI: – 69.3, – 10.1) reduced birth weight, 0.10 (95%CI: – 0.18, – 0.02) reduced birth weight z-score, and 0.02 g/cm3 (95%CI: – 0.04, – 0.00) reduced ponderal index. Ciprofloxacin, a preferred-as-veterinary antibiotic, showed a similar dose-response relationship with neonatal anthropometric parameters to florfenicol. However, these adverse effects diminished as children grew up to 12-, 24- and 60-month-old. Larger prospective cohort studies and animal experiments are warranted to verify the hypothesis that environmental antibiotics exposure in early life, even at low doses, may cause fetal growth restriction. [Display omitted] • Nearly three quarters of fetuses were exposed to low-dose veterinary antibiotics. • Prenatal veterinary antibiotics exposure may be inversely associated with birth weight. • Ciprofloxacin and florfenicol were the main contributors to the decreased fetal growth. • The adverse effects of veterinary antibiotics diminished as children grew up. [ABSTRACT FROM AUTHOR]

Polycyclic aromatic hydrocarbons (PAHs) are persistent organic pollutants in the environment, which are teratogenic, carcinogenic, and mutagenic. Co-contamination of PAHs and heavy metal commonly exists in soil. In this study, 20 types of soils with different properties in China were collected and comprehensively characterized. Phenanthrene (Phe) and Cu (II) were selected as representatives of PAHs and heavy metals, respectively. The adsorption-desorption behaviors of Phe under Phe contamination and Cu (II)-Phe co-contamination in 20 types of soils were studied. The adsorption-desorption behaviors of Phe in 20 types of soils varied greatly, and adsorption of Phe in the soils followed both linear partitioning and nonlinear surface adsorption. Soil organic matter (SOM) plays an important role in the adsorption-desorption behavior of Phe. When the concentrations of Phe were >50 μg/L, soft carbon (SC) fraction of SOM not black carbon (BC) contributed more to the adsorption of Phe. Soil dissolved organic matter (DOM), especially fulvic acid and humic acid fractions, contributes to the adsorption of Phe. Under the effect of Cu (II) (60 mg/L in solution), the adsorption capacity of soil for Phe increased, which possibly resulted from lowered pH, the existence of the cation-π bonding and the "bonding bridge" effect. The systematic investigation of adsorption-desorption behaviors of Phe in soils under heavy metal-PAHs co-contamination will provide a scientific basis for the calculation of soil environmental capacity in the future. [Display omitted] • Adsorption of Phe in soils with Cu (II)-Phe co-contamination exhibits both partitioning and surface adsorption. • The adsorption capacity of soil for Phe increases under co-contamination of Cu (II)-Phe. • Significant positive correlations were observed between Phe adsorption and SOM, SC in soils. [ABSTRACT FROM AUTHOR]

Nonylphenol (NP) contamination in the coastal environment of China poses ecological risks to aquatic organisms. However, the endocrine disruptive impacts of NP on bivalves, particularly on ovarian development, remain poorly understood. In this study, Manila clams Ruditapes philippinarum at the developing stage of gonad were exposed to 1.0 μg/L NP for 21 days. Utilizing RNA interference (RNAi) to suppress ER gene expression, we observed a delay in ovarian development as evidenced by histological observations under both NP and NPRi (NP with ER-RNAi) treatment, with Vtg elevation exclusive to the NP group. Comprehensive analyses encompassing transcriptomics, real-time quantitative PCR, and steroid hormone measurement revealed significant alterations in aldosterone synthesis, estrogen signaling, and thyroid hormone synthesis. These pathways showed similar perturbations in both NP and NPRi groups compared to controls. Notably, the NPRi group exhibited distinct enrichment in PPAR and insulin signaling pathways, may implicating these in ER function suppression. Steroid hormone biosynthesis was notably reduced in both treatments, pointing to a profound impact on hormone synthesis. The contrast between in vivo and in vitro findings suggests that NP's detrimental effects on ovarian development may primarily involve neuroendocrine regulation of steroidogenesis. This investigation highlights the complex dynamics of NP-induced endocrine disruption in bivalves, emphasizing the pivotal role of ER and associated pathways. [Display omitted] • NP accumulation leads to delayed ovarian development in clams. • NP accumulation induces the expression of ER and Vtg. • ER-RNAi clams shows no increased expression of Vtg after NP exposure. • Ovarian development cease may due to depressed steroids biosynthesis caused by NP exposure. [ABSTRACT FROM AUTHOR]

In recent years, the incidence of thyroid cancer has been on a significant rise worldwide, and a number of environmental factors have been suspected to be risk factors for thyroid cancer, especially the relationship between iodine intake and thyroid cancer has attracted attention. In this study, we want to assess the relationship between different water iodine exposures and thyroid cancer incidence before and after water alteration in areas with high water iodine in China. Thyroid cancer patients (2009–2020) were enrolled at two hospitals, both in Heze City, Shandong Province, an area with high water iodine levels. According to the criteria of the study, 5826 cases out of 8785 cases were selected for inclusion in the study. Before and after water alteration, the incidence of thyroid cancer was highest in areas with water iodine concentrations of 200–300 μg/L in high iodine areas. In areas where water iodine decreased to adequate iodine levels, there was a strong negative correlation between the decreased level of water iodine and the incidence of thyroid cancer. In addition, in cases with pathology reports, we found that the greater the decrease in water iodine values, the markedly smaller the maximum diameter of the thyroid cancer lesions. Taken together, these findings suggest that we should continue to monitor the incidence of thyroid cancer in areas with high water iodine and continue to optimize population iodine intake to reduce the incidence of thyroid cancer. [Display omitted] • Highest incidence of thyroid cancer found in areas with 200–300 μg/L water iodine. • Water iodine decline values negatively correlated with thyroid cancer incidence. • The lower water iodine levels, the smaller the diameter of thyroid cancer lesions. [ABSTRACT FROM AUTHOR]

In the present study, we investigated the occurrence, distribution, and potential risks of 4 brominated flame retardants in farmland soils across 18 provinces of China. The total mean concentrations of the BFRs were in order as DBDPE > BDE209 > HBB > TBB. DBDPE concentration was highest at 177.208 ng/kg, revealing its long-term use and persistence across the study areas. In parts of China, DBDPE was highest in the south (Sichuan, Shaanxi and Guangdong provinces), BDE209 was highest in the south (Sichuan province) and north (Jilin province), while HBB was highest in the south (Sichuan province) and east (Anhui and Zhejiang provinces) of China. Comparisons of the results in this study to other reported studies in different regions indicated that the studied BFRs concentrations were higher in the studied provinces of China. Pearson correlation between BFRs revealed both positive and negative associations within the BFRs groups and between BFRs and soil properties (SOM, CEC, pH, EC and PS%). The mean hazard quotients (HQ) of ecological risks ranged from 8.76 × 10−6 to 1.16 × 10−2 (HQ < 1) while non-carcinogenic human health risk evaluation for adults ranged from 7.05 × 10−7 - 7.48 × 10−4 (HQ < 1) and for children 2.99 × 10−4 - 4.30 × 10−2 (HQ < 1). Although the risk evaluations of BFRs from farmland soils in this study were low, the results serve as useful indicators of potential cumulative and long-term threats of BFR to rural areas where there is a high conversion of agricultural lands to non-agricultural use. [Display omitted] • BFRs concentrations from the typical farmland soils in China were evaluated. • BFRs distribution was the highest in the south and east parts of 18 provinces studied. • Dermal absorption and oral ingestion were main plausible exposure route for both children and adults. [ABSTRACT FROM AUTHOR]

Tetrabromobisphenol A (TBBPA), a currently intensively used brominated flame retardant (BFR), is employed primarily as a reactive flame retardant in printed circuit boards but also has additive applications in several types of polymers. TBBPA is a ubiquitous environmental contaminant that is observed in both abiotic and biotic matrices. This paper summarizes and critically reviews the published scientific data concerning the current pollution status of TBBPA in China. To provide an indication of the seriousness of the pollution levels of TBBPA in China, the data are compared with available existing data from other countries of the world. According to the available data, the sources of TBBPA in China are mainly derived from the primitive e-waste dismantling, TBBPA manufacturing and processing of TBBPA-based materials. The most serious cases of TBBPA pollution in China are in Guiyu, Guangdong (primitive e-waste dismantling site) with concentrations of TBBPA reaching 66,010–95,040 pg m −3 in air, Shouguang, Shandong (TBBPA manufacturing site) with concentrations of TBBPA reaching 1.64–7758 ng g −1 dry weight in soil, and Chaohu Lake, Anhui (industry concentration site) with concentrations of TBBPA reaching 850–4870 ng L −1 in water. In general, China is the most polluted region as affected by TBBPA compared with other countries. The present review preliminarily reveals the research status of TBBPA in China. [ABSTRACT FROM AUTHOR]

Abstract: Fulvic acids from the soil of Peking University (PF) and a Nordic river (NF) were separated into well defined sub-fractions using sequential elution techniques based on eluent polarity. The chemical properties of the fractions including: PF1 and NF1 (eluted by 0.01M HCl), PF2 and NF2 (eluted by 0.01M HCl+20% methanol), PF3 and NF3 (eluted by 0.01M HCl+40% methanol), and PF4 and NF4 (eluted by 100% methanol), were characterized using UV–Visible spectroscopy, elemental analysis and 13C NMR. The results showed that the UV absorptions of the elution peaks at 280nm (A280) increased from PF2 to PF4 and NF2 to NF4. No elution peaks were observed for PF1 and NF1. The carbon contents increased from 43.34% to 51.90% and 43.06% to 53.26% while the oxygen contents decreased from 46.39% to 36.76% and 49.76% to 40.03% for PF1–PF4 and NF1–NF4, respectively. As a polarity indicator, the (O+N)/C ratio for PF1–PF4 and NF1–NF4 decreased from 0.88 to 0.62 and 0.89 to 0.58, respectively. The aromatic carbon content increased from PF1 to PF4 and NF1 to NF4, suggesting an increase of the hydrophobicity of these fractions. The polarity was positively related to the ratio of UV absorption at 250nm and 365nm (E2/E3), and negatively related to the aromaticity. A high positive relationship between the aromaticity and E2/E3 of fulvic acid fractions was also obtained. The use of an eluent with a decreasing polarity allowed to providing simpler fractions of soil and aquatic fulvic acids. [Copyright &y& Elsevier]

Microbially-driven sulfur cycling is a vital biogeochemical process in the sulfur-rich mangrove ecosystem. It is critical to evaluate the potential impact of sulfur transformation in mangrove ecosystems. To reveal the diversity, composition, and structure of sulfur-oxidizing bacteria (SOB) and sulfate-reducing bacteria (SRB) and underlying mechanisms, we analyzed the physicochemical properties and sediment microbial communities from an introduced mangrove species (Sonneratia apetala), a native mangrove species (Kandelia obovata) and the mudflat in Hanjiang River Estuary in Guangdong (23.27°N, 116.52°E), China. The results indicated that SOB was dominated by autotrophic Thiohalophilus and chemoautotrophy Chromatium in S. apetala and K. obovata , respectively, while Desulfatibacillum was the dominant genus of SRB in K. obovata sediments. Also, the redundancy analysis indicated that temperature, redox potential (ORP), and SO 4 2− were the significant factors influencing the sulfur cycling microbial communities with elemental sulfur (ES) as the key factor driver for SOB and total carbon (TC) for SRB in mangrove sediments. Additionally, the morphological transformation of ES, acid volatile sulfide (AVS) and SO 4 2− explained the variation of sulfur cycling microbial communities under sulfur-rich conditions, and we found mangrove species-specific dominant Thiohalobacter , Chromatium and Desulfatibacillum, which could well use ES and SO 4 2−, thus promoting the sulfur cycling in mangrove sediments. Meanwhile, the change of nutrient substances (TN, TC) explained why SOB were more susceptible to environmental changes than SRB. Sulfate reducing bacteria produces sulfide in anoxic sediments at depth that then migrate upward, toward fewer reducing conditions, where it's oxidized by sulfur oxidizing bacteria. This study indicates the high ability of SOB and SRB in ES, SO 4 2− , S 2 − and S2− generation and transformation in sulfur-rich mangrove ecosystems, and provides novel insights into sulfur cycling in other wetland ecosystems from a microbial perspective. • S. apetala and K. obovata sediments had higher TC, ES and AVS. • The elemental sulfur was the key factor driving SOB, total carbon was the driving force for SRB in mangrove sediments. • SOB was more susceptible to environmental changes than SRB. [ABSTRACT FROM AUTHOR]

In China, the amount of phosphogypsum (PG) has exceeded 250 million tons with more than 55 million tons of growth rates each year. As the micro constituent, fluorine and phosphorus restrict the resourceful disposal of PG. This paper focused on chemical looping gasification (CLG) which used PG as an oxygen carrier, systematically investigated the gasification performance and chemical behavior of fluorine and phosphorus contained in PG during CLG process. Main conclusions are as follows. The main pollutant of chemical looping gasification process was HF, which was transformed from NaF. Phosphorus transformed from water-soluble phosphorus (Ca(H 2 PO 4) 2 , Ca(HPO 4)) into insoluble Ca 3 (PO 4) 2.20 reducing-oxidizing cycles were investigated, and a less and less fluorine content in oxygen carrier was found because its phase transformation from solid NaF to gaseous HF, and the phosphorus content in oxygen carrier changed slightly under the current conditions. The Ca 3 (PO 4) 2 particle layers existed in both the middle of the reduced solid particles and the middle of the cycled oxygen carrier particles, confirmed to actually act as a glue between the particles. Furthermore, transformation routes of fluorine and phosphorus during the CLG process were discussed and the generation of syngas in CLG process needed to be purified. Image 1 • Evaluate the gasification performance and fluorine and phosphorus chemical behavior in CLG using PG as an oxygen carrier. • The main pollutant was gaseous HF in CLG, which was transformed from NaF. • The Ca 3 (PO 4) 2 particle layer existed in the middle of the solid particles, acting as a glue between the particles. [ABSTRACT FROM AUTHOR]