HIV high risk population may face not only the threat of HIV infection but also a higher chance of exposure to environmental contaminants. However, no previous studies have examined the body burden of environmental pollutants including heavy metals among HIV high risk populations. The aim of this study was to investigate whether adults aged 20–59 years old at high risk of HIV infection have higher blood levels of heavy metals compared to those with low risk of HIV infection in United States.We used the National Health and Nutrition Examination Survey (NHANES) 1999–2010 to compare exposures to heavy metals including cadmium, lead, and total mercury by HIV risk status.The results showed that people at high risk of HIV had higher blood concentrations of all heavy metals compared to their counterparts with lower HIV risks. In multivariate linear regression models, HIV risk status was significantly associated with increased blood cadmium, lead, and total mercury after adjusting for age, sex, race, education, and poverty income ratio.Our study suggests that people at high risk of HIV have significantly higher body burden of heavy metals including cadmium, lead, and mercury compared to those with low risk of HIV. Further longitudinal study collecting more pollutants are warranted to determine the potential health effects of these elevated pollutants on both HIV-infected and HIV high-risk populations.

The most common mass spectrometry approach analyzing contamination of the environment deals with targeted analysis, i.e. detection and quantification of the selected (priority) pollutants. However non-targeted analysis is becoming more often the method of choice for environmental chemists. It involves implementation of modern analytical instrumentation allowing for comprehensive detection and identification of the wide variety of compounds of the environmental interest present in the sample, such as pharmaceuticals and their metabolites, musks, nanomaterials, perfluorinated compounds, hormones, disinfection by-products, flame retardants, personal care products, and many others emerging contaminants. The paper presents the results of detection and identification of previously unreported organic compounds in snow samples collected in Moscow in March 2016. The snow analysis allows evaluation of long-term air pollution in the winter period. Gas chromatography coupled to a high resolution time-of-flight mass spectrometer has enabled us with capability to detect and identify such novel analytes as iodinated compounds, polychlorinated anisoles and even Ni-containing organic complex, which are unexpected in environmental samples. Some considerations concerning the possible sources of origin of these compounds in the environment are discussed.

Volatile organic compounds (VOCs) from two sampling sites (HB and XB) in a power station centralized area, in Shuozhou city, China, were sampled by stainless steel canisters and measured by gas chromatography-mass selective detection/flame ionization detection (GC-MSD/FID) in the spring and autumn of 2014. The concentration of VOCs was higher in the autumn (HB, 96.87 μg/m3; XB, 58.94 μg/m3) than in the spring (HB, 41.49 μg/m3; XB, 43.46 μg/m3), as lower wind speed in the autumn could lead to pollutant accumulation, especially at HB, which is a new urban area surrounded by residential areas and a transportation hub. Alkanes were the dominant group at both HB and XB in both sampling periods, but the contribution of aromatic pollutants at HB in the autumn was much higher than that of the other alkanes (11.16–19.55%). Compared to other cities, BTEX pollution in Shuozhou was among the lowest levels in the world. Because of the high levels of aromatic pollutants, the ozone formation potential increased significantly at HB in the autumn. Using the ratio analyses to identify the age of the air masses and analyze the sources, the results showed that the atmospheric VOCs at XB were strongly influenced by the remote sources of coal combustion, while at HB in the spring and autumn were affected by the remote sources of coal combustion and local sources of vehicle emission, respectively. Source analysis conducted using the Positive Matrix Factorization (PMF) model at Shuozhou showed that coal combustion and vehicle emissions made the two largest contributions (29.98% and 21.25%, respectively) to atmospheric VOCs. With further economic restructuring, the influence of vehicle emissions on the air quality should become more significant, indicating that controlling vehicle emissions is key to reducing the air pollution.

With the increasing production and applications of TiO2 nanoparticles (NPs), their presence in aquatic environments, especially in sediments, will inevitably increase over time. Most studies investigating the influence of TiO2 NPs on the bioaccumulation of co-existing contaminants have focused on the aqueous phase; however, few have examined the sediment phase, which contains more TiO2 NPs and contaminants. We investigated the effects of TiO2 NPs on Pb accumulation by Corbicula fluminea in sediments, and explored extracellular and intracellular Pb concentrations in the various soft tissues of the bivalve. Pb was spiked with 50 mg/kg in sediment and TiO2 NPs/sediments ratios were within the range 0.2–3.0%. The results showed that TiO2 NPs presented larger adsorption capacity and affinity to Pb ions than the sediments. In addition, the large adsorption capacity of TiO2 NPs and the strong adsorption affinity to Pb ions caused part of the Pb ions released from sediments to aqueous phase were re-adsorbed by TiO2 NPs in sediments. The concentration of TiO2 NPs in C. fluminea tissues significantly increased with increasing TiO2 NP content in sediments, following the order: gill > mantle > foot > visceral mass, which differed from the results found in the aqueous phase. In addition, the proportions of extracellular and intracellular Pb concentrations changed significantly in all the tissues as a result of TiO2 NP contamination of sediments. TiO2 NPs promote increased extracellular Pb in foot, mantle, and gill tissues, and increased intracellular Pb in the visceral mass. These results may be beneficial to more scientifically evaluate and predict the environmental risks of TiO2 NPs to benthic organisms in sediments contaminated by heavy metals.

The impacts of iron oxide nanoparticles (γ-Fe2O3 NPs) and ferric ions (Fe³⁺) on plant growth and molecular responses associated with the transformation and transport of Fe²⁺ were poorly understood. This study comprehensively compared and evaluated the physiological and molecular changes of Citrus maxima plants as affected by different levels of γ-Fe2O3 NPs and Fe³⁺. We found that γ-Fe2O3 NPs could enter plant roots but no translocation from roots to shoots was observed. 20 mg/L γ-Fe2O3 NPs had no impact on plant growth. 50 mg/L γ-Fe2O3 NPs significantly enhanced chlorophyll content by 23.2% and root activity by 23.8% as compared with control. However, 100 mg/L γ-Fe2O3 NPs notably increased MDA formation, decreased chlorophyll content and root activity. Although Fe³⁺ ions could be used by plants and promoted the synthesis of chlorophyll, they appeared to be more toxic than γ-Fe2O3 NPs, especially for 100 mg/L Fe³⁺. The impacts caused by γ-Fe2O3 NPs and Fe³⁺ were concentration-dependent. Physiological results showed that γ-Fe2O3 NPs at proper concentrations had the potential to be an effective iron nanofertilizer for plant growth. RT-PCR analysis showed that γ-Fe2O3 NPs had no impact on AHA gene expression. 50 mg/L γ-Fe2O3 NPs and Fe³⁺ significantly increased expression levels of FRO2 gene and correspondingly had a higher ferric reductase activity compared to both control and Fe(II)-EDTA exposure, thus promoting the iron transformation and enhancing the tolerance of plants to iron deficiency. Relative levels of Nramp3 gene expression exposed to γ-Fe2O3 NPs and Fe³⁺ were significantly lower than control, indicating that all γ-Fe2O3 NPs and Fe³⁺ treatments could supply iron to C. maxima seedlings. Overall, plants can modify the speciation and transport of γ-Fe2O3 NPs or Fe³⁺ for self-protection and development by activating many physiological and molecular processes.

Wheat is one of several cereals that is capable of accumulating higher amounts of Cd in plant tissues. It is important to understand the Cd²⁺ transport processes in roots that result in excess Cd accumulation. Traditional destructive technologies have limited capabilities in analyzing root samples due to methodological limitations, and sometimes may result in false conclusions. The mechanisms of Cd²⁺ uptake into the roots of wheat seedlings (Triticum aestivum L.) were investigated by assessing the impact of various inhibitors and channel blockers on Cd accumulation as well as the real-time net Cd²⁺ flux at roots with the non-destructive scanning ion-selective electrode technique. The P-type ATPase inhibitor Na3VO4 (500 μM) had little effect on Cd uptake (p < 0.05) and the kinetics of transport in the root of wheat, suggesting that Cd²⁺ uptake into wheat root cells is not directly dependent on H⁺ gradients. While, the uncoupler 2,4-dinitrophenol significantly limited Cd²⁺ uptake (p < 0.05) and transport kinetics in the root of wheat, suggesting the existence of metabolic mediation in the Cd²⁺ uptake process by wheat. The Cd content at the whole-plant level in wheat was significantly (p < 0.05) decreased upon pretreatment with the Ca²⁺ channel blockers La³⁺ or Gd³⁺ and Verapamil, but not in case of pretreatment with the K⁺ channel blocker tetraethylammonium (TEA). In addition, the inhibitors of the Ca²⁺ channel, as well as high concentrations of Ca²⁺, reduced the real-time net Cd²⁺ fluxes at the root surface in SIET experiments. These results indicate that Cd²⁺ moves across the plasma lemma of the wheat root via Ca²⁺ channels. In addition, our results suggested a role for protein synthesis in mediating Cd²⁺ uptake and transport by wheat.

Heze city, a medium-size city in Shandong province, Eastern China. Ambient PM2.5 samples were collected in urban area of Heze from August 2015 to April 2016, and chemical species and sources of PM2.5 were investigated in this paper. The results indicated that the average concentration of PM2.5 was 100.9 μg/m3 during the sampling period, and the water-soluble ions, carbonaceous species included elemental carbon (EC) and organic carbon (OC), as well as elements contributed 32.7–51.7%, 16.3% and 12.5%, respectively, to PM2.5. Pearson's correlation analysis showed that the existing form of NH4+ was more complex and diverse in spring/summer, and ammonium nitrate, ammonium sulfate and ammonium hydrogen sulfate might be major form of NH4+ in autumn/winter. Correlation analysis between PM2.5 and SO42−/NO3−, PM2.5 and OC/EC during different seasons suggested that mobile sources might make an important impact on the increase of PM2.5 concentrations in spring/summer, and stationary sources might play a critical role on the increase of PM2.5 concentrations in autumn/winter. Seven factors were selected in Positive Matrix Factorization (PMF) models analysis based on the Error Estimation (EE) diagnostics during different seasons. Secondary source had the highest contribution to PM2.5 in Heze for the whole year, and followed by coal combustion, vehicle exhaust, soil dust, construction dust, biomass burning and metal manufacturing, and their annual contributions to PM2.5 were 26.5%, 17.2%, 16.5%, 11.5%, 7.7%, 7.0% and 3.8%, respectively. The air masses that were originated from Mongolia reflected the features of large-scale and long-distance air transport; while the air masses that began in Jiangsu, Shandong and Henan showed the features of small-scale and short-distance. Shandong, Henan and Jiangsu were identified as the major potential sources-areas of PM2.5 by using potential source contribution function (PSCF) and concentration-weighted trajectory (CWT) models.

Portmán Bay is a heavily contaminated area resulting from decades of metal mine tailings disposal, and is considered a suitable shallow-water analogue to investigate the potential ecotoxicological impact of deep-sea mining. Resuspension plumes were artificially created by removing the top layer of the mine tailings deposit by bottom trawling. Mussels were deployed at three sites: i) off the mine tailings deposit area; ii) on the mine tailings deposit beyond the influence from the resuspension plumes; iii) under the influence of the artificially generated resuspension plumes. Surface sediment samples were collected at the same sites for metal analysis and ecotoxicity assessment. Metal concentrations and a battery of biomarkers (oxidative stress, metal exposure, biotransformation and oxidative damage) were measured in different mussel tissues. The environmental hazard posed by the resuspension plumes was investigated by a quantitative weight of evidence (WOE) model that integrated all the data. The resuspension of sediments loaded with metal mine tails demonstrated that chemical contaminants were released by trawling subsequently inducing ecotoxicological impact in mussels’ health. Considering as sediment quality guidelines (SQGs) those indicated in Spanish action level B for the disposal of dredged material at sea, the WOE model indicates that the hazard is slight off the mine tailings deposit, moderate on the mine tailings deposit without the influence from the resuspension plumes, and major under the influence of the resuspension plumes. Portmán Bay mine tailings deposit is a by-product of sulphide mining, and despite differences in environmental setting, it can reflect the potential ecotoxic effects to marine fauna from the impact of resuspension of plumes created by deep-sea mining of polymetallic sulphides. A similar approach as in this study could be applied in other areas affected by sediment resuspension and for testing future deep-sea mining sites in order to assess the associated environmental hazards.

In this study water balance components as well as nitrogen and dissolved organic carbon leaching were quantified by means of large weighable grassland lysimeters at three sites (860, 770 and 600 m a.s.l.) for both intensive and extensive management. Our results show that at E600, the site with highest air temperature (8.6 °C) and lowest precipitation (981.9 mm), evapotranspiration losses were 100.7 mm higher as at the site (E860) with lowest mean annual air temperature (6.5 °C) and highest precipitation (1359.3 mm). Seepage water formation was substantially lower at E600 (−440.9 mm) as compared to E860. Compared to climate, impacts of management on water balance components were negligible. However, intensive management significantly increased total nitrogen leaching rates across sites as compared to extensive management from 2.6 kg N ha−1 year−1 (range: 0.5–6.0 kg N ha−1 year−1) to 4.8 kg N ha−1 year−1 (range: 0.9–12.9 kg N ha−1 year−1). N leaching losses were dominated by nitrate (64.7%) and less by ammonium (14.6%) and DON (20.7%). The low rates of N leaching (0.8–6.9% of total applied N) suggest a highly efficient nitrogen uptake by plants as measured by plant total N content at harvest. Moreover, plant uptake was often exceeding slurry application rates, suggesting further supply of N due to soil organic matter decomposition. The low risk of nitrate losses via leaching and surface runoff of cut grassland on non-sandy soils with vigorous grass growth may call for a careful site and region specific re-evaluation of fixed limits of N fertilization rates as defined by e.g. the German Fertilizer Ordinance following requirements set by the European Water Framework and Nitrates Directive.

Microcystin-leucine arginine (MC-LR) causes testicular inflammation and hinders spermatogenesis. However, the molecular mechanisms underlying the immune responses to MC-LR in the testis have not been elucidated in detail. In this study, we show that MC-LR induced immune responses in Sertoli cells (SC), germ cells (GC), and Leydig cells (LC) via activating phosphatidylinositol 3-kinase (PI3K)/AKT/nuclear factor kappa B (NF-κB), resulting in the production of pro-inflammatory cytokines and chemokines including tumor necrosis factor alpha (TNF-α), interleukin-6 (IL-6), monocyte chemoattractant protein-1 (MCP-1), and chemokine (C-X-C motif) ligand 10 (CXCL10). The observed effects were attributed to reduced activity of protein phosphatases 2A (PP2A) as a result of binding of MC-LR to the catalytic subunit of PP2A in SC and GC. By contrast, innate immune responses were triggered by Toll-like receptor 2 (TLR2) in LC because MC-LR could not enter into the LC and subsequently inhibit the PP2A activity. PI3K/AKT/NF-κB were also activated in SC, GC, and LC in vivo, with the enrichment of TNF-α, IL-6, MCP-1, and CXCL10 in the testis. Following chronic exposure, MC-LR-treated mice exhibited decreased sperm counts and abnormal sperm morphology. Our data demonstrate that MC-LR can activate innate immune responses in testicular cells, which provides novel insights to explore the mechanism associated with MC-LR-induced orchitis.