Guangdong-Hongkong-Macau Joint Laboratory of Collaborative Innovation for Environmental Quality

Abstract The overall water splitting efficiency is mainly restricted by the slow kinetics of oxygen evolution. Therefore, it is essential to develop active oxygen evolution catalysts. In this context, we designed and synthesized a tungsten oxide catalyst with oxygen vacancies for photocatalytic oxygen evolution, which exhibited a higher oxygen evolution rate of 683 μmol h −1 g −1 than that of pure WO 3 (159 μmol h −1 g −1 ). Subsequent studies through transient absorption spectroscopy found that the oxygen vacancies can produce electron trapping states to inhibit the direct recombination of photogenerated carriers. Additionally, a Pt cocatalyst can promote electron trap states to participate in the reaction to improve the photocatalytic performance further. This work uses femtosecond transient absorption spectroscopy to explain the photocatalytic oxygen evolution mechanism of inorganic materials and provides new insights into the design of high‐efficiency water‐splitting catalysts.

Adiponectin (ADN) is an adipocyte-secreted protein with insulin-sensitizing, antidiabetic, antiinflammatory, and antiatherogenic properties. Evidence is also accumulating that ADN has neuroprotective activities, yet the underlying mechanism remains elusive. Here we show that ADN could pass through the blood-brain barrier, and elevating its levels in the brain increased cell proliferation and decreased depression-like behaviors. ADN deficiency did not reduce the basal hippocampal neurogenesis or neuronal differentiation but diminished the effectiveness of exercise in increasing hippocampal neurogenesis. Furthermore, exercise-induced reduction in depression-like behaviors was abrogated in ADN-deficient mice, and this impairment in ADN-deficient mice was accompanied by defective running-induced phosphorylation of AMP-activated protein kinase (AMPK) in the hippocampal tissue. In vitro analyses indicated that ADN itself could increase cell proliferation of both hippocampal progenitor cells and Neuro2a neuroblastoma cells. The neurogenic effects of ADN were mediated by the ADN receptor 1 (ADNR1), because siRNA targeting ADNR1, but not ADNR2, inhibited the capacity of ADN to enhance cell proliferation. These data suggest that adiponectin may play a significant role in mediating the effects of exercise on hippocampal neurogenesis and depression, possibly by activation of the ADNR1/AMPK signaling pathways, and also raise the possibility that adiponectin and its agonists may represent a promising therapeutic treatment for depression.

Recent studies have reported a variety of health consequences of climate change. However, the vulnerability of individuals and cities to climate change remains to be evaluated. We project the excess cause-, age-, region-, and education-specific mortality attributable to future high temperatures in 161 Chinese districts/counties using 28 global climate models (GCMs) under two representative concentration pathways (RCPs). To assess the influence of population ageing on the projection of future heat-related mortality, we further project the age-specific effect estimates under five shared socioeconomic pathways (SSPs). Heat-related excess mortality is projected to increase from 1.9% (95% eCI: 0.2-3.3%) in the 2010s to 2.4% (0.4-4.1%) in the 2030 s and 5.5% (0.5-9.9%) in the 2090 s under RCP8.5, with corresponding relative changes of 0.5% (0.0-1.2%) and 3.6% (-0.5-7.5%). The projected slopes are steeper in southern, eastern, central and northern China. People with cardiorespiratory diseases, females, the elderly and those with low educational attainment could be more affected. Population ageing amplifies future heat-related excess deaths 2.3- to 5.8-fold under different SSPs, particularly for the northeast region. Our findings can help guide public health responses to ameliorate the risk of climate change.

While there has been extensive investigation into modulating quasi-2D perovskite compositions in light-emitting diodes (LEDs) for promoting their electroluminescence, very few reports have studied approaches involving enhancement of the energy transfer between quasi-2D perovskite layers of the film, which plays very important role for achieving high-performance perovskite LEDs (PeLEDs). In this work, a bifunctional ligand of 4-(2-aminoethyl)benzoic acid (ABA) cation is strategically introduced into the perovskite to diminish the weak van der Waals gap between individual perovskite layers for promoting coupled quasi-2D perovskite layers. In particular, the strengthened interaction between coupled quasi-2D perovskite layers favors an efficient energy transfer in the perovskite films. The introduced ABA can also simultaneously passivate the perovskite defects by reducing metallic Pb for less nonradiative recombination loss. Benefiting from the advanced properties of ABA incorporated perovskites, highly efficient blue PeLEDs with external quantum efficiency of 10.11% and a very long operational stability of 81.3 min, among the best performing blue quasi-2D PeLEDs, are achieved. Consequently, this work contributes an effective approach for high-performance and stable blue PeLEDs toward practical applications.

p-Phenylenediamines (PPDs) are widely used as antioxidants in tire rubber, and their derived quinone transformation products (PPD-Qs) may pose a threat to marine ecosystems. A compelling example is N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD)-derived quinone, called 6PPD-Q, as the causal toxicant for stormwater-linked acute mortality toward coho salmon. However, the knowledge of the co-occurrences of PPDs and PPD-Qs and their transport from freshwater to oceanic waterbodies on a large geographical scale remains unknown. Herein, we performed the first large-scale survey of these chemicals in sediments across urban rivers, estuaries, coasts, and deep-sea regions. Our results demonstrated that seven PPDs and four PPD-Qs are ubiquitously present in riverine, estuarine, and coastal sediments, and most of them also occur in deep-sea sediments. The most dominant chemicals of concern were identified as 6PPD and 6PPD-Q. Total sedimentary concentrations of PPDs and PPD-Qs presented a clear spatial trend with decreasing levels from urban rivers (medians: 39.7 and 15.2 ng/g) to estuaries (14.0 and 5.85 ng/g) and then toward coasts (9.47 and 2.97 ng/g) and deep-sea regions (5.24 and 3.96 ng/g). Interestingly, spatial variation in the ratios of 6PPD to 6PPD-Q (R6PPD/6PPD-Q) also presented a clear decreasing trend. Our field measurements implied that riverine outflows of PPDs and PPD-Qs may be an important route to transport these tire rubber-derived chemicals to coastal and open oceans.

N-(1,3-Dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD) and its quinone derivative, 6PPD-quinone (6PPD-Q), have been found to be prevalent in the environment, but there are currently no data on their presence in humans. Herein, we conducted the first human biomonitoring study of 6PPD and 6PPD-Q by measuring 150 urine samples collected from three different populations (general adults, children, and pregnant women) in South China. Both 6PPD and 6PPD-Q were detected in the urine samples, with detection frequencies between 60% and 100%. Urinary 6PPD-Q concentrations were significantly higher than those of 6PPD and correlated well with those of 6PPD (p < 0.01), indicating coexposure to 6PPD and 6PPD-Q in humans. In vitro metabolic experiments demonstrated rapid depletion of 6PPD by human liver microsomes, which should be responsible for the lower concentrations of 6PPD in human urine. Additionally, pregnant women exhibited apparently higher concentrations of 6PPD and 6PPD-Q (median 0.068 and 2.91 ng/mL, respectively) than did adults (0.018 and 0.40 ng/mL) and children (0.015 and 0.076 ng/mL). The high daily urinary excretion of 6PPD-Q in pregnant women was estimated to be 273 (ng/kg bw)/day. Considering that 6PPD-Q was a lethal toxicant to multiple aquatic species, the potential human health risks posed by its long-term exposure require urgent attention.

Curcumenol, an effective ingredient of Wenyujin, has been reported that exerted its antitumor potential in a few cancer types. However, the effect and molecular mechanism of curcumenol in lung cancer are largely unknown. Here, we found that curcumenol induced cell death and suppressed cell proliferation in lung cancer cells. Next, we demonstrated that ferroptosis was the predominant method that contributed to curcumenol-induced cell death of lung cancer in vitro and vivo for the first time. Subsequently, using RNA sequencing, we found that the long non-coding RNA H19 (lncRNA H19) was significantly downregulated in lung cancer cells treated with curcumenol, when compared to untreated controls. Overexpression of lncRNA H19 eliminated the anticancer effect of curcumenol, while lncRNA H19 knockdown promoted ferroptosis induced by curcumenol treatment. Mechanistically, we showed that lncRNA H19 functioned as a competing endogenous RNA to bind to miR-19b-3p, thereby enhanced the transcription activity of its endogenous target, ferritin heavy chain 1 (FTH1), a marker of ferroptosis. In conclusion, our data show that the natural product curcumenol exerted its antitumor effects on lung cancer by triggering ferroptosis, and the lncRNA H19/miR-19b-3p/FTH1 axis plays an essential role in curcumenol-induced ferroptotic cell death. Therefore, our findings will hopefully provide a valuable drug for treating lung cancer patients.

Due to the widespread use of medicine in recent years, antibiotics as the emerging pollutants have been widely detected in the aquatic environment. To address this situation, developing advanced treatment technologies to effectively remove antibiotics are emergently needed. Photocatalysis for the removal of antibiotics driven by sunlight has been considered a promising technology, due to its green, environmentally friendly, and cost-effective properties. Currently, great efforts have been done to construct highly efficient photocatalytic oxidation systems for the degradation of antibiotic pollutants. To be updated, we herein summary the recent progress on the removal of antibiotic pollutants using the photocatalytic oxidation process within the last 5 years. We begin by introducing the classification, structures, and environmental hazards of common antibiotics. Subsequently, the fundamental mechanism of photocatalytic degradation of antibiotics is presented and the details on the degradation information of the different kinds of antibiotics via semiconductors photocatalysts are discussed and listed. Finally, we present a brief discussion on the opportunities and challenges remaining in photocatalytic removal of antibiotic pollutants.

Abstract The long‐term operational stability of perovskite light‐emitting diodes (PeLEDs), especially red PeLEDs with only several hours typically, has always faced great challenges. Stable β‐CsPbI 3 nanocrystals (NCs) are demonstrated for highly efficient and stable red‐emitting PeLEDs through incorporation of poly(maleic anhydride‐ alt ‐1‐octadecene) (PMA) in synthesizing the NCs. The PMA can chemically interact with PbI 2 in the precursors via the coupling effect between O groups in PMA and Pb 2+ to favor crystallization of stable β‐CsPbI 3 NCs. Meanwhile, the cross‐linked PMA significantly reduces the Pb Cs anti‐site defect on the surface of the β‐CsPbI 3 NCs. Benefiting from the improved crystal phase quality, the photoluminescence quantum yield for β‐CsPbI 3 NCs films remarkably increases from 34% to 89%. The corresponding red‐emitting PeLEDs achieves a high external quantum efficiency of 17.8% and superior operational stability with the lifetime, the time to half the initial electroluminescence intensity ( T 50 ) reaching 317 h at a constant current density of 30 mA cm −2 .

Nanoplastic uptake in plants has drawn increasing attention for its potential toxicity to organisms at higher trophic levels. However, the mechanisms remain ambiguous due to the lack of quantitative methods for nanoplastic uptake in plants. Herein, a novel procedure incorporating alkaline digestion, cellulose precipitation, and ultrasonic leaching, followed by pyrolysis gas chromatography–mass spectrometry (Py-GC/MS) analysis, was developed to quantify nanoplastic uptake in plants with cucumber (Cucumis sativus) as the model species. Recoveries of 81.6%–97.2% were obtained for polystyrene (PS) and poly(methyl methacrylate) (PMMA) nanoplastics at spiking levels of 34.5–61.5 μg/g in quality control samples. Detection limits of 2.31–4.15 μg/g for PS and 3.87–8.20 μg/g for PMMA nanoplastics were achieved. After exposure to 50 mg/L of 100 nm PS nanoplastics for 7 and 14 days, 0–6893 μg/g nanoplastics were detected in various dried cucumber tissues using the developed method with their presence identified by scanning electron microscopy (SEM), suggesting nanoplastic uptake, translocation, and accumulation in plants. Comparative experiments with inductively coupled plasma mass spectrometry (ICP-MS) using palladium-labeled nanoplastics further confirmed the promising application of our method in quantifying nanoplastic uptake in plants. Consequently, the proposed method provides new possibilities for screening nanoplastics in plants.

Abstract. Volatile organic compounds (VOCs) play important roles in the tropospheric atmosphere. In this study, VOCs were measured at an urban site in Guangzhou, one of the megacities in the Pearl River Delta (PRD), using a gas chromatograph–mass spectrometer/flame ionization detection (GC–MS/FID) and a proton transfer reaction time-of-flight mass spectrometer (PTR-ToF-MS). Diurnal profile analyses show that stronger chemical removal by OH radicals for more reactive hydrocarbons occurs during the daytime, which is used to estimate the daytime average OH radical concentration. In comparison, diurnal profiles of oxygenated volatile organic compounds (OVOCs) indicate evidence of contributions from secondary formation. Detailed source analyses of OVOCs, using a photochemical age-based parameterization method, suggest important contributions from both primary emissions and secondary formation for measured OVOCs. During the campaign, around 1700 ions were detected in PTR-ToF-MS mass spectra, among which there were 462 ions with noticeable concentrations. VOC signals from these ions are quantified based on the sensitivities of available VOC species. OVOC-related ions dominated PTR-ToF-MS mass spectra, with an average contribution of 73 % ± 9 %. Combining measurements from PTR-ToF-MS and GC–MS/FID, OVOCs contribute 57 % ± 10 % to the total concentration of VOCs. Using concurrent measurements of OH reactivity, OVOCs measured by PTR-ToF-MS contribute greatly to the OH reactivity (19 % ± 10 %). In comparison, hydrocarbons account for 21 % ± 11 % of OH reactivity. Adding up the contributions from inorganic gases (48 % ± 15 %), ∼ 11 % (range of 0 %–19 %) of the OH reactivity remains `missing”, which is well within the combined uncertainties between the measured and calculated OH reactivity. Our results demonstrate the important roles of OVOCs in the emission and evolution budget of VOCs in the urban atmosphere.

The prediction of RNA three-dimensional structures remains an unsolved problem. Here, we report assessments of RNA structure predictions in CASP15, the first CASP exercise that involved RNA structure modeling. Forty-two predictor groups submitted models for at least one of twelve RNA-containing targets. These models were evaluated by the RNA-Puzzles organizers and, separately, by a CASP-recruited team using metrics (GDT, lDDT) and approaches (Z-score rankings) initially developed for assessment of proteins and generalized here for RNA assessment. The two assessments independently ranked the same predictor groups as first (AIchemy_RNA2), second (Chen), and third (RNAPolis and GeneSilico, tied); predictions from deep learning approaches were significantly worse than these top ranked groups, which did not use deep learning. Further analyses based on direct comparison of predicted models to cryogenic electron microscopy (cryo-EM) maps and x-ray diffraction data support these rankings. With the exception of two RNA-protein complexes, models submitted by CASP15 groups correctly predicted the global fold of the RNA targets. Comparisons of CASP15 submissions to designed RNA nanostructures as well as molecular replacement trials highlight the potential utility of current RNA modeling approaches for RNA nanotechnology and structural biology, respectively. Nevertheless, challenges remain in modeling fine details such as noncanonical pairs, in ranking among submitted models, and in prediction of multiple structures resolved by cryo-EM or crystallography.

Abstract. The atmospheric processes under polluted environments involving interactions of anthropogenic pollutants and natural emissions lead to the formation of various and complex secondary products. Therefore, the characterization of oxygenated organic compounds in urban areas remains a pivotal issue in our understanding of the evolution of organic carbon. Here, we describe measurements of an iodide chemical ionization time-of-flight mass spectrometer installed with a Filter Inlet for Gases and AEROsols (FIGAERO-I-CIMS) in both the gas phase and the particle phase at an urban site in Guangzhou, a typical megacity in southern China, during the autumn of 2018. Abundant oxygenated organic compounds containing two to five oxygen atoms were observed, including organic acids, multi-functional organic compounds typically emitted from biomass burning, oxidation products of biogenic hydrocarbons and aromatics. Photochemistry played dominant roles in the formation of gaseous organic acids and isoprene-derived organic nitrates, while nighttime chemistry contributed significantly to the formation of monoterpene-derived organic nitrates and inorganics. Nitrogen-containing organic compounds occupied a significant fraction of the total signal in both the gas and particle phases, with elevated fractions at higher molecular weights. Measurements of organic compounds in the particle phase by FIGAERO-I-CIMS explained 24 ± 0.8 % of the total organic aerosol mass measured by aerosol mass spectrometer (AMS), and the fraction increased for more aged organic aerosol. The systematical interpretation of mass spectra of the FIGAERO-I-CIMS in the urban area of Guangzhou provides a holistic view of numerous oxygenated organic compounds in the urban atmosphere, which can serve as a reference for the future field measurements by FIGAERO-I-CIMS in polluted urban regions.

The persistent COVID-19 pandemic since 2020 has brought an enormous public health burden to the global society and is accompanied by various evolution of the virus genome. The consistently emerging SARS-CoV-2 variants harboring critical mutations impact the molecular characteristics of viral proteins and display heterogeneous behaviors in immune evasion, transmissibility, and the clinical manifestation during infection, which differ each strain and endow them with distinguished features during populational spread. Several SARS-CoV-2 variants, identified as Variants of Concern (VOC) by the World Health Organization, challenged global efforts on COVID-19 control due to the rapid worldwide spread and enhanced immune evasion from current antibodies and vaccines. Moreover, the recent Omicron variant even exacerbated the global anxiety in the continuous pandemic. Its significant evasion from current medical treatment and disease control even highlights the necessity of combinatory investigation of the mutational pattern and influence of the mutations on viral dynamics against populational immunity, which would greatly facilitate drug and vaccine development and benefit the global public health policymaking. Hence in this review, we summarized the molecular characteristics, immune evasion, and impacts of the SARS-CoV-2 variants and focused on the parallel comparison of different variants in mutational profile, transmissibility and tropism alteration, treatment effectiveness, and clinical manifestations, in order to provide a comprehensive landscape for SARS-CoV-2 variant research.

An increasing population, climate change, and diminishing natural resources present severe threats to global food security, with traditional breeding and genetic engineering methods often falling short in addressing these rapidly evolving challenges. CRISPR/Cas systems have emerged as revolutionary tools for precise genetic modifications in crops, offering significant advancements in resilience, yield, and nutritional value, particularly in staple crops like rice and maize. This review highlights the transformative potential of CRISPR/Cas technology, emphasizing recent innovations such as prime and base editing, and the development of novel CRISPR-associated proteins, which have significantly improved the specificity, efficiency, and scope of genome editing in agriculture. These advancements enable targeted genetic modifications that enhance tolerance to abiotic stresses as well as biotic stresses. Additionally, CRISPR/Cas plays a crucial role in improving crop yield and quality by enhancing photosynthetic efficiency, nutrient uptake, and resistance to lodging, while also improving taste, texture, shelf life, and nutritional content through biofortification. Despite challenges such as off-target effects, the need for more efficient delivery methods, and ethical and regulatory concerns, the review underscores the importance of CRISPR/Cas in addressing global food security and sustainability challenges. It calls for continued research and integration of CRISPR with other emerging technologies like nanotechnology, synthetic biology, and machine learning to fully realize its potential in developing resilient, productive, and sustainable agricultural systems.

Fine particulate matter (with aerodynamic diameter ≤2.5 µm, PM2.5) causes huge disease burden worldwide. However, evidence is still inadequate and inconsistent on the relationships between PM2.5 constituents and mortality, especially in low resource settings. To evaluate the impact of PM2.5 constituents on cause-specific mortality in China. We obtained daily mortality data for 161 communities in 2011–2013 from the Disease Surveillance Point system in China. Daily concentrations of major PM2.5 constituents, including organic carbon (OC), elemental carbon (EC), sulphate (SO42-), nitrate (NO3-) and ammonium (NH4+), were estimated by using the modified Community Multiscale Air Quality model. For each community, we applied quasi-Poisson regression and polynomial distributed lag models to estimate the effects of PM2.5 constituents on cause-specific mortality. Then, the pooled effect estimates were calculated by a random-effect meta-analysis based on the restricted maximum likelihood estimation. Stratification analyses were performed by region, gender, age group and education level to identify the vulnerable populations. Each interquartile range change of EC, OC, SO42-, NO3- and NH4+ at lag 0–3 day was associated with increments in non-accidental mortality of 0.45% (95%CI: 0.21, 0.69), 1.43% (0.97, 1.89), 0.71% (0.28, 1.15), 0.70% (0.10, 1.30) and 0.95% (0.39, 1.51), respectively. The associations were stronger for the deaths from cardiovascular disease and myocardial infarction, the elderly, illiterates, and people living in the South region. Our findings suggest positive associations between PM2.5 constituents and cause-specific mortality, particularly for myocardial infarction.

responses, indicating that future emission control shall be regionally specific, instead of one-size-fits-all cut. Overall, the importance of regionally coordinated and balanced control strategy for multiple pollutants is highly emphasized.

Our previous study demonstrated massive emissions of liquid crystal monomers (LCMs) from liquid crystal display (LCD)-associated e-waste dismantling; however, the compositions, priority list, and inventory of LCMs in waste LCD panels remain unknown. Herein, we conducted the first comprehensive identification covering a broader range of LCMs, including 21 biphenyls and analogues (BAs), 28 cyanobiphenyls and analogues (CBAs), and 44 fluorinated biphenyls and analogues (FBAs), in waste television/computer LCD panels. A total of 64 of the 93 target LCMs, including 19 BAs, 6 CBAs, and 39 FBAs, were widely detected in collected waste LCD panels. Approximately 10-18 of the 64 detectable LCMs were identified as the main compositions in various waste LCD panels, which contributed to >90% of the total LCMs. Total concentrations of FBAs in the television/computer LCD panel samples were comparable to those of BAs but much higher than those of CBAs, indicating FBAs and BAs being the commonly used LCM categories. The composition distribution of LCMs varied between television/computer LCDs and among different brands of television/computer LCDs. A preliminary estimate of the globally direct release of LCMs from waste television/computer LCD panels into various environmental compartments was about 1.07-107 kg/year, which will increase considerably in the near future.

Liquid-crystal monomers (LCMs), especially fluorinated biphenyls and analogues (FBAs), are considered to be a new generation of persistent, bioaccumulative, and toxic organic pollutants, but their emissions from liquid-crystal display (LCD)-associated e-waste dismantling remain unknown. To fill this knowledge gap, a broad range of 46 LCMs, including 39 FBAs and 7 biphenyls/bicyclohexyls and analogues (BAs), were investigated by a dedicated target analysis in e-waste dust samples. Of 39 target FBAs, 34 were detected in LCD dismantling-associated dust. Among these 34 detectable FBAs, 9 were detected in 100% of the samples and 25 were frequently detected in >50% of the samples. The total concentrations of these 34 FBAs (∑34FBAs) detected in LCD e-waste dust were in the range of 225–976,000 (median: 18,500) ng/g, significantly higher than those in non-LCD e-waste dust (range: 292–18,500, median: 2300 ng/g). In addition to FBAs, six of seven BAs were also frequently detected in LCD e-waste dust with total concentrations (∑6BAs) of 29.8–269,000 (median: 3470) ng/g. Very strong and significant correlations (P < 0.01) were identified in all frequently detected LCMs, indicating their common applications and similar sources. Our findings demonstrate that e-waste dismantling contributes elevated emissions of FBAs and BAs to the ambient environment.

Numerous studies have reported the environmental contamination with traditional organophosphate triesters (tri-OPEs), but there is very little information on emerging tri-OPEs and organophosphate diesters (di-OPEs), especially in e-waste recycling areas. In this study, we conducted a comprehensive survey to monitor a broad suite of 11 traditional tri-OPEs, 12 emerging OPEs, and 10 di-OPEs in indoor dust collected from the workshops of (n = 42) and residential homes adjacent to (n = 24) a mega e-waste recycling industrial park in South China. In addition to traditional tri-OPEs, all of the emerging OPEs and di-OPEs were frequently detected in the dust samples. Total concentrations of emerging tri-OPEs and di-OPEs were in the range of 1210–62 900 and 2010–55 600 ng/g in the workshop dust and 435–23 700 and 186–4350 ng/g in the local home dust, respectively, which were comparable to those of traditional tri-OPEs (1160–61 500 and 370–13 900 ng/g, respectively). Most OPEs exhibited significantly higher concentrations in workshop dust versus local home dust (p < 0.05), indicating that e-waste dismantling activities contributed to the high residues of OPEs in indoor dust. Correlation analysis revealed that tri-OPEs have some common emission sources, i.e., e-waste and household products, while di-OPEs could originate from different sources, e.g., tri-OPE degradation, direct commercial application, and impurities in tri-OPE formulas. For both occupational workers and local adults, the median estimated daily intake values of emerging tri-OPEs (7.5 and 1.7 ng/kg bw/day, respectively) and di-OPEs (3.9 and 0.2 ng/kg bw/day, respectively) were comparable to that of traditional tri-OPEs (4.3 and 1.0 ng/kg bw/day, respectively), which suggests the important contribution of the emerging tri-OPEs and di-OPEs to the overall risks of human external exposure to OPE chemicals.