Occurrence and fate of current-use pesticides in Chinese forest soils.

Pesticides play a crucial role in securing global food production to meet increasing demands. However, because of their pervasive use, they are now ubiquitous environmental pollutants that have adverse effects on both ecosystems and human health. In this study, the environmental occurrence and fate of 16 current-use pesticides (CUPs) were investigated in 93 forest soil samples obtained from 11 distinct mountains in China. The concentrations of the target pesticides ranged from 0.36 to 55 ng/g dry weight. Cypermethrin, dicofol, chlorpyrifos, chlorothalonil, and trifluralin were the most frequently detected CUPs. The CUP concentrations were generally higher in the O-horizon than in the A-horizon. Chlorpyrifos, chlorothalonil, and dicofol were detected in most deep layers in soil profiles from three mountains selected to represent distinct climate zones. No clear altitudinal trend in organic carbon-normalized concentrations of CUPs was observed in the O- or A-horizons within individual mountains. A negative correlation was noted between the CUP concentrations and the altitudes across all sampling sites. This indicated that proximity to emission sources was a key factor affecting the spatial distribution of CUPs in mountain forest soil on a national scale. The ecological risk assessment showed that dicofol and cypermethrin pose potential risks to earthworms. This study emphasizes the importance of source control when setting management strategies for CUPs.

Mapping the Contribution of Biomass Burning to Persistent Organic Pollutants in the Air of the Indo-China Peninsula Based on a Passive Air Monitoring Network.

Biomass burning (BB) is an important source of atmospheric persistent organic pollutants (POPs) across the world. However, there are few field-based regional studies regarding the POPs released from BB. Due to the current limitations of emission factors and satellites, the contribution of BB to airborne POPs is still not well understood. In this study, with the simultaneous monitoring of BB biomarkers and POPs based on polyurethane foam-based passive air sampling technique, we mapped the contribution of BB to polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in the Indo-China Peninsula. Spearman correlations between levoglucosan and 16 PCBs (rs = 0.264-0.767, p < 0.05) and 2 OCPs (rs = 0.250-0.328, p < 0.05) confirmed that BB may facilitate POP emissions. Source apportionment indicated that BB contributed 9.3% to the total PCB and OCP mass. The high contribution of positive matrix factorization-resolved BB to PCBs and OCPs was almost consistent with their concentration distributions in the open BB season but not completely consistent with those in the pre-monsoon and/or monsoon seasons. Their contribution distributions may reflect the use history and geographic distribution in secondary sources of POPs. The field-based contribution dataset of BB to POPs is significant in improving regional BB emission inventories and model prediction.

Provenance of Aerosol Black Carbon over Northeast Indian Ocean and South China Sea and Implications for Oceanic Black Carbon Cycling.

Aerosol black carbon (BC) is a short-lived climate pollutant. The poorly constrained provenance of tropical marine aerosol BC hinders the mechanistic understanding of extreme climate events and oceanic carbon cycling. Here, we collected PM2.5 samples during research cruise NORC2016-10 through South China Sea (SCS) and Northeast Indian Ocean (NEIO) and measured the dual-carbon isotope compositions (δ13C-Δ14C) of BC using hydrogen pyrolysis technique. Aerosol BC exhibits six different δ13C-Δ14C isotopic spaces (i.e., isotope provinces). Liquid fossil fuel combustion, from shipping emissions and adjacent land, is the predominant source of BC over isotope provinces "SCS close to Chinese Mainland" (53.5%), "Malacca Strait" (53.4%), and "Open NEIO" (40.7%). C3 biomass burning is the major contributor to BC over isotope provinces "NEIO close to Southeast Asia" (55.8%), "Open NEIO" (41.3%), and "Open SCS" (40.0%). Coal combustion and C4 biomass burning show higher contributions to BC over "Sunda Strait" and "Open SCS" than the others. Overall, NEIO near the Bay of Bengal, Malacca Strait, and north SCS are three hot spots of fossil fuel-derived BC; the first two areas are also hot spots of biomass-derived BC. The comparable δ13C-Δ14C between BC in aerosol and dissolved BC in surface seawater may suggest atmospheric BC deposition as a potential source of oceanic dissolved BC.

Probing Legacy and Alternative Flame Retardants in the Air of Chinese Cities.

An increasing number of alternative flame retardants (FRs) are being introduced, following the international bans on the use of polybrominated diphenyl ether (PBDE) commercial mixtures. FRs' production capacity has shifted from developed countries to developing countries, with China being the world's largest producer and consumer of FRs. These chemicals are also imported with e-waste to China. Therefore, it is important to understand the current status of regulated brominated FRs, their phase-out in China, and their replacement by alternatives. In this study, a broad suite of legacy and alternative FRs, including eight PBDEs, six novel brominated FRs (NBFRs), two dechlorane plus variants (DPS), and 12 organophosphate FRs (OPFRs) were evaluated in the air of 10 large Chinese cities in 2018. OPFRs are the most prevalent FRs in China, exhibiting a wide range of 1-612 ng/m3, which is several orders of magnitude higher than PBDEs (1-1827 pg/m3) and NBFRs (1-1428 pg/m3). BDE 209 and DBDPE are the most abundant compounds in brominated FRs (>80%). The North China Plain (NCP, excluding Beijing), Guangzhou, and Lanzhou appear to be three hotspots, although with different FR patterns. From 2013/2014 to 2018, levels of PBDEs, NBFRs, and DPs have significantly decreased, while that of OPFRs has increased by 1 order of magnitude. Gas-particle partitioning analysis showed that FRs could have not reached equilibrium, and the steady-state model is better suited for FRs with a higher log KOA (>13). To facilitate a more accurate FR assessment in fine particles, we suggest that, in addition to the conventional volumetric concentration (pg/m3), the mass-normalized concentration (pg/g PM2.5) could also be used.

Polycyclic Aromatic Carbon: A Key Fraction Determining the Light Absorption Properties of Methanol-Soluble Brown Carbon of Open Biomass Burning Aerosols.

The composition and radiative forcing of light-absorbing brown carbon (BrC) aerosol remain poorly understood. Polycyclic aromatics (PAs) are BrC chromophores with fused benzene rings. Understanding the occurrence and significance of PAs in BrC is challenging due to a lack of standards for many PAs. In this study, we quantified polycyclic aromatic carbon (PAC), defined as the carbon of fused benzene rings, based on molecular markers (benzene polycarboxylic acids, BPCAs). Open biomass burning aerosols (OBBAs) of 22 rainforest plants were successively extracted with water and methanol for the analysis of water- and methanol-soluble PAC (WPAC and MPAC, respectively). PAC is an important fraction of water- and methanol-soluble organic carbon (WSOC and MSOC, respectively). WPAC/WSOC ranged from 0.03 to 0.18, and MPAC/MSOC was even higher (range: 0.16-0.80). The priority polycyclic aromatic hydrocarbons contributed less than 1% of MPAC. The mass absorption efficiency (MAE) of MSOC showed a strong linear correlation with MPAC/MSOC (r = 0.60-0.95, p < 0.01). The absorption Ångström exponent (AAE) of methanol-soluble BrC showed a strong linear correlation with the degree of aromatic condensation of MPAC, which was described by the average number of carboxylic groups of BPCA (r = -0.79, p < 0.01). This result suggested that PAC was a key fraction determining the light absorption properties (i.e., light absorptivity and wavelength dependence) of methanol-soluble BrC in OBBAs.

DDT, Chlordane, and Hexachlorobenzene in the Air of the Pearl River Delta Revisited: A Tale of Source, History, and Monsoon.

Although organochlorine pesticides (OCPs) have been banned for more than three decades, their concentrations have only decreased gradually. This may be largely attributable to their environmental persistence, illegal application, and exemption usage. This study assessed the historic and current regional context for dichlorodiphenyltrichloroethane (DDT), chlordane, and hexachlorobenzene (HCB), which were added to the Stockholm Convention in 2001. An air sampling campaign was carried out in 2018 in nine cities of the Pearl River Delta (PRD), where the historical OCP application was the most intensive in China. Different seasonalities were observed: DDT exhibited higher concentrations in summer than in winter; chlordane showed less seasonal variation, whereas HCB was higher in winter. The unique coupling of summer monsoon with DDT-infused paint usage, winter monsoon with HCB-combustion emission, and local chlordane emission jointly presents a dynamic picture of these OCPs in the PRD air. We used the BETR Global model to back-calculate annual local emissions, which accounted for insignificant contributions to the nationally documented production (<1‰). Local emissions were the main sources of p,p'-DDT and chlordane, while ocean sources were limited (<4%). This study shows that geographic-anthropogenic factors, including source, history, and air circulation pattern, combine to affect the regional fate of OCP compounds.

High Abundance of Unintentionally Produced Tetrachlorobiphenyls (PCB47/48/75, 51, and 68) in the Atmosphere at a Regional Background Site in East China.

Although polychlorinated biphenyls (PCBs) have been banned for several decades, they are still detected with elevated levels due to their unintentional production from combustion and industrial thermal processes (UP-PCBs). To investigate the composition and current levels of UP-PCBs and understand which sources are controlling PCB burdens in ambient atmosphere, air samples were collected from August 2012 to August 2015 at a background site in east China. An unexpected high abundance of PCB47+48+75 was observed to be the predominant congener with an average concentration of 786 ± 637 pg/m3. It accounted for 48 ± 16% of ΣPCBs, followed by PCB51 (10 ± 4%), PCB11 (8 ± 6%), and PCB68 (7 ± 3%). Seasonal variations with high levels in summer and lowest levels in winter were observed for PCB47+48+75, 51, and 68. These tetrachlorobiphenyl congeners were strongly correlated with temperature ( r2 > 0.7), suggesting the control of temperature-dependent volatilization processes from contaminated surfaces. The decreased occurrence of PCB47+48+75, 51, and 68 in commercial products and their negative correlations (| r| < 0.35) with polycyclic aromatic hydrocarbon (PAHs) and weak correlation with other PCB congeners suggested unique unintentional sources that differ from combustion and industrial thermal processes or pigment, such as the use of polymer sealant, for PCB47+48+75, 51, and 68 in the ambient air.

Using Polyurethane Foam-Based Passive Air Sampling Technique to Monitor Monosaccharides at a Regional Scale.

Monosaccharides are important tracers of pollution aerosol from biomass burning. Air sampling of monosaccharides is often conducted using active samplers. However, applicability of sampling monosaccharides using polyurethane foam passive air samplers (PUF-PASs) has not been investigated, since passive air samplers are often applied to monitor semivolatile organic contaminants in large scale and remote area. Our study successfully collected atmospheric monosaccharides using PUF-PASs, providing a valuable tool for monosaccharides sampling. PUF-PAS sampling rates for individual monosaccharides were calibrated using an active sampler for 92 days, and were 1.1, 1.5, and 1.1 m3/d for levoglucosan, mannosan, and galactosan, respectively. Degradation of monosaccharides in PUF-PAS was demonstrated to be negligible by spike test of 13C-labeled levoglucosan. Furthermore, passive sampling was carried out at 11 sites in the Pearl River Delta of Southern China from January to April and July to September of 2015. Monosaccharide concentrations derived from PUF-PASs were comparable with the reported data obtained by active sampling, demonstrating that the PUF-PAS approach is valid for monosaccharides monitoring. On the basis of our approach, we found that there is a clear correlation between the monosaccharide concentrations and the MODIS fire activities during January-April.

Highly responsive hydrazine sensors based on donor-acceptor perylene diimides: impact of electron-donating groups.

Three high-performance hydrazine sensing devices have been developed based on donor-acceptor perylenediimides (PDIs) with strongly electron-donating piperidinyl (PDI-PY), pyrrolidinyl (PDI-PI) and n-hexylamino (PDI-HE) as substituents at the perylene core. These PDI devices, compared with reported PDI molecules, displayed 1-2 orders of magnitude higher sensitivity, short response/recovery time and a lower detection limit towards hydrazine vapour. Experimental results demonstrated that PDI-HE possessed the most excellent sensing performance due to its larger electron density and well-defined crystalline structure with a smaller π-π distance of 3.55 Å, yet, poor crystalline structure, weak π-π orbital overlap as well as a larger interplanar spacing of 3.62 Å led to the poorest sensing performance of PDI-PY devices. This study clearly reveals that electron-donating substituents can remarkably improve the sensing performance of PDI devices by increasing the density of electrons, meanwhile, the steric hindrance of electron-donating groups can modulate the sensing performance by influencing the crystalline structure, π-π overlap and π-π distance. The excellent sensing performance makes donor-acceptor perylenes one of the candidates with the most potential for fabrication of highly efficient PDI sensing devices.

Experimental Study on the Role of Sedimentation and Degradation Processes on Atmospheric Deposition of Persistent Organic Pollutants in a Subtropical Water Column.

The goal of this study is to experimentally assess the role of vertical sinking and degradation processes of persistent organic pollutants (POPs) in a subtropical water column. This was done by measuring the concentrations of selected typical organochlorine pesticides, including hexachlorocyclohexanes (HCHs), hexachlorobenzene (HCB), dichlorodiphenyltrichloroethanes (DDTs), trans-chlordane (TC), and cis-chlordane (CC), in atmosphere (gas phase), water (dissolved and particulate phases), and sedimentation samples simultaneously from October 2011 to April 2013 in a subtropical lake. The fugacity ratios suggested net deposition for α-HCH, γ-HCH, p,p'-DDT, p,p'-DDD, p,p'-DDE, o,p'-DDT, TC, and CC, indicating that the subtropical lake was acting as a "sink" for these chemicals. The enantiomer fractions of α-HCH, o,p'-DDT, TC, and CC in the dissolved phase samples were much more deviated from the racemic values than were those in the air samples, suggesting that these chemicals have suffered microbial degradation in the subtropical lake. In fact, 99% to 100% of atmospheric input of α-HCH and γ-HCH to the subtropical lake was estimated to be depleted via microbial degradation, while the role of hydrolysis and vertical sinking was very small. For more hydrophobic p,p'-DDT, o,p'-DDT, TC, and CC, the role of vertical sinking was 2 to 3 orders of magnitude larger than that for α-HCH and γ-HCH. Microbial degradation was also very important for removing p,p'-DDT, o,p'-DDT, TC, and CC from the water column.

Targeted protein degradation in hematologic malignancies: latest updates from the 2023 ASH annual meeting.

Protein degraders, emerging as a novel class of therapeutic agents, have gained widespread attention due to their advantages. They have several advantages over traditional small molecule inhibitors, including high target selectivity and ability to target "undruggable" targets and overcome inhibitor drug resistance. Tremendous research and development efforts and massive investment have resulted in rapid advancement of protein degrader drug discovery in recent years. Here, we overview the latest clinical and preclinical updates on protein degraders presented at the 2023 ASH Annual Meeting.

Molecular signatures and formation mechanisms of water-soluble chromophores in particulate matter from Karachi in Pakistan.

Excitation-emission matrix (EEM) fluorescence spectroscopy is a widely-used method for characterizing the chemical components of brown carbon (BrC). However, the molecular basics and formation mechanisms of chromophores, which are decomposed by parallel factor (PARAFAC) analysis, are not yet fully understood. In this study, we characterized the water-soluble organic carbon (WSOC) in aerosols collected from Karachi, Pakistan, using EEM spectroscopy and Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). We identified three PARAFAC components, including two humic-like components (C1 and C2) and one phenolic-like species (C3). We determined the molecular families associated with each component by performing Spearman correlation analysis between FT-ICR MS peaks and PARAFAC component intensities. We found that the C1 and C2 components were associated with nitrogen-enriched compounds, where C2 with the longest emission wavelength exhibited a higher level of aromaticity, N content, and oxygenation than C1. The C3 associated formulas have fewer nitrogen-containing species, a lower unsaturation degree, and a lower oxidation state. An oxidation pathway was identified as an important process in the formation of C1 and C2 components at the molecular level, particularly for the assigned CHON compounds associated with the gas-phase oxidation process, despite their diverse precursor types. Numerous C2 formulas were found in the "potential BrC" region and overlapped with the BrC-associated formulas. It can be inferred that the compounds that fluoresce C2 contributed considerably to the light absorption of BrC. These findings are essential for future studies utilizing the EEM-PARAFAC method to explore the sources, processes, and compositions of atmospheric BrC.

Benzene polycarboxylic acids as molecular markers of black carbon: Progresses and challenges.

Black carbon (BC) is generated as a result of the pyrolysis of biomass and fossil fuels. Different approaches have been taken to analyse BC in the environment, including thermal, optical and chemical methods. The chemical approach which uses benzene polycarboxylic acids (BPCAs) as molecular markers of BC has gained popularity within the scientific community recently. These pyrogenic molecular markers can be used to reconstruct ancient fire history and human presence. Here we review the development of the BPCA protocols for the analysis of BC and the previous studies that have used these methods. Additionally, this review explores the biogeochemical factors that influence the content and composition of BPCAs, which in turn affect the sources attributed to BC. These factors include the generation temperature of char, photodegradation, biodegradation and the interference of non-pyrogenic organic matter (OM) in BPCA-BC analysis. Different combustion temperatures can yield charred BC with varying degrees of aromatic condensation throughout the BC continuum, while aged soot-BC undergoes photochemical degradation, causing the loss of its original condensed aromatic structure. Photodegradation reduces the degree of BC condensation by preferentially breaking down the most condensed forms, whereas biodegradation primarily mineralizes the smaller and more biolabile BC. Non-pyrogenic sources, such as humic acids (HAs), have been found to contribute up to 25% of BPCA-BC in soil, and their presence can lead to overestimations of BC. Future research should focus on calibrating contemporary BPCA protocols using known reference materials and investigating the role of non-pyrogenic OM in BPCA-BC analysis.

Characteristics of dissolved black carbon in riverine surface microlayer.

Black carbon (BC) is produced by the incomplete combustion of biomass and fossil fuels. The dissolved form of BC (DBC), which is transported through rivers into the oceans, is of great significance for the carbon cycling on the planet due to its refractory features. However, the characteristics and sources of DBC in riverine water are poorly constrained. Here, we analyzed DBC contents and stable carbon isotope (δ13C) signatures in surface microlayer (SML) from the upper, middle and lower reaches of Pearl River (PR) in the first study of its kind. The DBC contents (100.9 to 166.6 µg L-1) in SML were lower than the global average for riverine water following a trend of upper > middle > lower reaches in PR. The molecular markers of DBC (BPCAs) and their δ13C values showed no statistical differences between the sampling sites (p > 0.05), suggesting biomass burning as the dominant source.

Distribution and air-sea exchange of current-use pesticides (CUPs) from East Asia to the high Arctic Ocean.

Surface seawater and marine boundary layer air samples were collected on the ice-breaker R/V Xuelong (Snow Dragon) from the East China Sea to the high Arctic (33.23-84.5° N) in July to September 2010 and have been analyzed for six current-use pesticides (CUPs): trifluralin, endosulfan, chlorothalonil, chlorpyrifos, dacthal, and dicofol. In all oceanic air samples, the six CUPs were detected, showing highest level (>100 pg/m(3)) in the Sea of Japan. Gaseous CUPs basically decreased from East Asia (between 36.6 and 45.1° N) toward Bering and Chukchi Seas. The dissolved CUPs in ocean water ranged widely from

Characterization of airborne PAHs and metals associated with PM10 fractions collected from an urban area of Sri Lanka and the impact on airway epithelial cells.

Airborne particulate matter (PM), polycyclic aromatic hydrocarbons (PAHs) and heavy metals (HMs) are significant contributors leading to many human health issues. Thus, this study was designed to perform chemical analysis and biological impact of airborne particulate matter 10 (PM10) in the World heritage City of Kandy City in Sri Lanka. 12 priority PAHs and 34 metals, including 10 highly toxic HMs were quantified. The biological effects of organic extracts were assayed using an in vitro primary porcine airway epithelial cell culture model. Cytotoxicity, DNA damage, and gene expressions of selected inflammatory and cancer-related genes were also assessed. Results showed that the total PAHs ranged from 3.062 to 36.887 ng/m3. The metals were dominated by Na > Ca > Mg > Al > K > Fe > Ti, while a few toxic HMs were much higher in the air than the existing ambient air quality standards. In the bioassays, a significant cytotoxicity (p < 0.05) was observed at 300 µg/mL treatment, and significant (p < 0.05) DNA damages were noted in all treatment groups. All genes assessed were found to be significantly up-regulated (p < 0.05) after 24 h of exposure and after 48 h, only TGF-ß1 and p53 did not significantly up-regulate (p < 0.05). These findings confirm that the Kandy city air contains potential carcinogenic and mutagenic compounds and thus, exposure to Kandy air may increase the health risks and respiratory tract-related anomalies.

Oxidative potential of solvent-extractable organic matter of ambient total suspended particulate in Bangkok, Thailand.

Oxidative stress is a key mechanism by which ambient particulate matter induces adverse health effects. Most studies have focused on the oxidative potential (OP) of water-soluble constituents, while there has been limited work on the OP of solvent-extractable organic matter (EOM OP). In this study, the EOM OP of ambient total suspended particulate (TSP) from Bangkok, Thailand, was determined using the dithiothreitol (DTT) assay. Positive matrix factorization (PMF), combined with chemical analysis of molecular markers, was employed to apportion the contributions of various emission sources to EOM OP. The volume-normalized OP initially increased with organic carbon (OC) concentration and plateaued gradually, while the mass-normalized OP fitted well with OC concentration using a power function. Fossil fuel combustion (62%) and plastic waste burning (23%) were the major contributors to EOM OP, while biomass burning demonstrated only a limited contribution. EOM OP correlated well with each group of polycyclic aromatic hydrocarbons (PAHs), suggesting that secondary formation of quinones associated with fossil fuel combustion and plastic waste burning could be an important pathway of TSP toxicity. This study underscores the importance of considering different emission sources when evaluating potential health impacts and the implementation of air pollution regulations.

Development of a novel pyroptosis-related LncRNA signature with multiple significance in acute myeloid leukemia.

Background: Pyroptosis, a programmed cell death (PCD) with highly inflammatory form, has been recently found to be associated with the origin of hematopoietic malignancies. Long noncoding RNA (lncRNA) had emerged as an essential mediator to regulate gene expression and been involved in oncogenesis. However, the roles of pyroptosis-related lncRNA (PRlncRNA) in acute myeloid leukemia (AML) have not yet been completely clarified. Methods: We collected AML datasets from public databases to obtain PRlncRNA associated with survival and constructed a PRlncRNA signature using Lasso-Cox regression analysis. Subsequently, we employed RT-PCR to confirm its expression difference and internal training to further verify its reliability. Next, AML patients were classified into two subgroups by the median risk score. Finally, the differences between two groups in immune infiltration, enrichment analysis and drug sensitivity were further explored. Results: A PRlncRNA signature and an effective nomogram combined with clinicopathological variables to predict the prognosis of AML were constructed. The internal validations showed that the PRlncRNA risk score model was an accurate and productive indicator to predict the outcome of AML. Furthermore, this study indicated that higher inflammatory cell and immunosuppressive cells, and less sensitive to conventional chemotherapy drugs were highlighted in the high-risk group. Conclusion: Through comprehensive analysis of PRlncRNA model, our study may offer a valuable basis for future researches in targeting pyroptosis and tumor microenvironment (TME) and provide new measures for prevention and treatment in AML.

Regional monitoring of biomass burning using passive air sampling technique reveals the importance of MODIS unresolved fires.

Field-based sampling can provide more accurate evaluation than MODIS in regional biomass burning (BB) emissions given the limitations of MODIS on unresolved fires. Polyurethane foam-based passive air samplers (PUF-PASs) are a promising tool for collecting atmospheric monosaccharides. Here, we deployed PUF-PASs to monitor monosaccharides and other BB-related biomarkers and presented a dataset of 31 atmospheric BB-related biomarkers in the Indo-China Peninsula (ICP) and Southwest China. The peak concentrations of monosaccharides in the ICP occurred before monsoon season. The highest concentrations were in the eastern Mekong plain, while the lowest were along the eastern coast. BB-related biomarkers displayed elevated concentrations after April, particularly in the monsoon season; however, fewer active fires were recorded by MODIS. This revealed the importance of MODIS unresolved fires (e.g., indoor biofuel combustion, small-scale BB incidents, and charcoal fires) to the regional atmosphere. The PAS derived levoglucosan concentrations indicated that, with the inclusion of MODIS unresolved fires, the estimated top-down emissions of PM (4194-4974 Gg/yr), OC (1234-1719 Gg/yr) and EC (52-384 Gg/yr) would be higher than previous bottom-up estimations in the ICP. Future studies on these MODIS unresolved fires and regional monitoring data of BB are vital for improving the modeling of regional BB emissions.