Contamination and health risks brought by arsenic, lead and cadmium in a water-soil-plant system nearby a non-ferrous metal mining area.

Heavy metal(loid)s contamination prevails in the water-soil-plant system around non-ferrous metal mining areas. The present study aimed to evaluate the heavy metal(loid)s contamination in Nandan Pb-Zn mining area (Guangxi, China). A total of 36 river water samples, 75 paired paddy soil and rice samples, and 128 paired upland soil and plant samples were collected from this area. The concentrations of arsenic (As), lead (Pb), and cadmium (Cd) in these samples were measured. Results showed that the average water quality indexes (WQIs) at the 12 sampling sites along the main river ranged from 41 to 5008, indicating the water qualities decreasing from "Excellent" to "Undrinkable". The WQIs nearby tailings or industrial park were significantly higher than those at the other sites. 34.0% and 64.5% of soil samples exceeded the risk screening values for As and Cd. The Pb and Cd concentrations in all rice samples exceeded the Chinese food safety limits by 18.7% and 82.7%, respectively. Leafy vegetables had a higher concentration of As, Pb, and Cd than other vegetables, exceeding the maximum permissible limits by 14.1%, 61.2%, and 40.0%, respectively. The biological accumulation coefficient (BAC) of Cd was the highest in rice and lettuce leaves. The hazard quotients (HQs) of As and Cd, indicating non-carcinogenic risks, were 4.15 and 1.76 in adult males, and 3.40 and 1.45 in adult females, all higher than the permitted level (1.0). The carcinogenic probabilities of As and Cd from rice and leafy vegetables consumption were all higher than 1 × 10-4. We conclude that metal(loid)s contamination of the water-soil-plant system has posed great non-carcinogenic and carcinogenic risks to the local population.

[Characterization of Ambient Volatile Organic Compounds, Source Apportionment, and the Ozone-NOx-VOC Sensitivities in Liucheng County, Guangxi].

Liucheng county, as a suburb of Liuzhou City in Guangxi province, has a prominent ozone (O3) pollution problem; however, there have been no relevant analyses of the cause of local O3 pollution reported. In order to investigate the causes of O3 pollution, an online observation of 116 VOCs with a time resolution of 1 h was carried out in Liucheng county from October 1st to 15th, and the sensitivity of ozone to the relative changes in the NOx and VOCs was analyzed. The results showed that the average value of φï¼»total volatile organic compounds (TVOCs)ï¼½ during the observation period was 27.52×10-9, and the average value of φ(TVOCs) during the polluting process (October 1st to 6th) was 32.15×10-9, which was 32.79% higher than that of the non-pollution process (October 8th to 15th). In terms of species concentration, oxygenated volatile organic compounds (OVOCs) contributed the highest, accounting for 43.70%, followed by alkanes (23.00%), aromatics (11.75%), and halocarbons (7.35%). In terms of ozone formation potential (OFP), OVOCs contributed the highest (41.96%) to OFP, followed by aromatics (32.60%) and alkenes (17.92%). During the observation period, VOCs mainly came from motor vehicle emissions (32.44%), biomass combustion sources (29.31%), solvent use sources (16.43%), plant sources (11.34%), and chemical industry emissions (10.49%). The contribution ratios of solvent use sources and plant sources in the pollution process increased by 28.58% and 28.53%, respectively. The EKMA curve shows that, during the observation period, Liucheng county was in a synergistic control area for VOCs and nitric oxide (NOx). Therefore, in the high ozone-occurrence autumn of Liucheng county, the key will be to reduce both VOCs and NOx emissions.

[Nonlinear Response Relationship Between Ozone and Precursor Emissions in the Pearl River Delta Region Under Different Transmission Channels].

With the rapid development of urbanization, ozone (O3) pollution is an ongoing occurrence in the Pearl River Delta (PRD) region in China. The effective control of O3 pollution is a great challenge owing to the nonlinear relationship between O3 and precursor emissions and the effect of meteorological conditions. Based on the regional air quality model CAMx-OSAT (ozone source apportionment technology), O3 formation regimes were determined, and inter-city transportation across PRD was quantified under different transmission channels. The results showed that spatial differences were observed for the O3 formation regimes under different transmission channels. The VOCs-sensitive regime was mainly located in the central areas of the PRD region, and the NOx-sensitive regime was distributed in the suburban areas of the PRD regions under calm wind conditions. When the northeast wind was prevailing, the polluted air mass of the urban agglomeration was transmitted southwesterly downward, resulting in the downwind areas being transformed to VOCs-sensitive; the upwind areas were still NOx-sensitive. Under the southeast wind, the VOCs-sensitive regime had a banding distribution along the southeast-northwest direction, and the remaining areas were NOx-sensitive. With the influence of transmission channels, downwind cities were significantly affected by the transmission of upwind urban agglomerations (41%-87%), whereas the local formation was the main contributor under the calm wind conditions (60%-87%). To explore the relationship between O3 and precursor emissions, a series of sensitivity tests were designed. The results showed that maximized areas (20%-36%) with reductions in O3 can be achieved by reducing VOCs and NOx in the corresponding sensitive regimes, and the maximized level with the reduction in O3 can be fulfilled by reducing VOCs in the VOCs-sensitive regime. For the typical city Jiangmen, the area that met the standard increased the most under the calm wind (11%) and southeast wind (8%) conditions when VOCs and NOx were reduced in the corresponding sensitive regimes. Additionally, under northeast wind conditions, reducing VOCs in the VOCs-sensitive regime can more effectively control O3, as the area up to the standard increased by 140%.

[Characteristics and Meteorological Factors of Complex Nonattainment Pollution of Atmospheric Photochemical Oxidant (Ox) and PM2.5 in the Pearl River Delta Region, China].

Based on the atmospheric pollutant data from twelve monitoring sites in the Guangdong-Hong Kong-Macao Pearl River Delta Regional Air Quality Monitoring Network, the mass concentration trends of atmospheric photochemical oxidants (Ox, NO2+O3) and PM2.5 during 2013-2017 were studied. The complex nonattainment pollution of Ox and PM2.5 is defined as the daily average mass concentration of NO2 and PM2.5 and daily maximum 8 h average (O3 MDA8) mass concentration of O3 simultaneously that exceeds the Chinese grade Ⅱ national air quality standard. The characteristics and meteorological factors that influence the complex nonattainment pollution of Ox and PM2.5 at different types of areas were analyzed. The results indicate that from 2013 to 2017, the annual average mass concentration of PM2.5 in the Pearl River Delta (PRD) region decreased from (44±7) µg·m-3 to (32±4) µg·m-3, which met the annual standard for three consecutive years. The annual average mass concentration of Ox decreased from (127±14) µg·m-3 in 2013 to (114±12) µg·m-3 in 2016 and then showed a general rebound trend to (129±13) µg·m-3 in 2017 when O3 concentrations increased significantly (10 µg·m-3). The proportion of pollution processes with O3 as the primary pollutant increased from 33% in 2013 to 78% in 2017, and the regional characteristics of simultaneous pollution in multiple cities have been highlighted. The complex nonattainment pollution of Ox and PM2.5 occurred 60 times during the study period, primarily in urban sites (78%) and suburban sites (22%). The largest number of days of complex nonattainment pollution occurred in autumn (52%) because of strong solar radiation that was conducive to ozone formation, and consequently, the high oxidization of the atmosphere promoted the secondary generation of PM2.5. The weather conditions that caused the complex nonattainment pollution in the PRD mainly include outflow-high-pressures (43%), subtropical-high-pressures(30%), and tropical-depressions (27%). In terms of specific meteorological conditions, when the temperature was in the range of 20-25℃ and relative humidity was in the range of 60%-75%, the proportion of complex nonattainment pollution was the highest (22%). When O3 pollution was substantial, the high relative humidity and low wind speed during the nighttime caused the concentration of NO2 and PM2.5 to rise significantly, and then the high temperatures during the day aggravated the complex nonattainment pollution.

[Characteristics of Organic and Elemental Carbon in PM10 and PM2.5 in Yulin City, Guangxi].

Two hundred eighteen PM10 and 202 PM2.5 samples were collected at three sampling sites to study the pollution characteristics of carbonaceous aerosols in Yulin from July 2015 to March 2016. Organic carbon (OC) and elemental carbon (EC) in the PM10 and PM2.5 samples were analyzed by a Multiwavelength Thermal/Optical Carbon Analyzer, and the characteristics, including pollution levels, temporal and spatial distributions, and possible sources of OC and EC, were investigated. The results showed that the OC and EC mass concentrations in PM10 in Yulin were 10.99 and 5.11 µg·m-3, respectively, while the OC and EC mass concentrations in PM2.5 were 7.51 and 4.70 µg·m-3, respectively. Strong correlations between OC and EC were found in PM10(R2=0.58) and PM2.5(R2=0.60). The winter average concentrations of secondary organic carbon (SOC) in PM10 and PM2.5 were 14.50 µg·m-3 and 6.74 µg·m-3, respectively. The SOC/OC ratios in both the PM10 and PM2.5 were higher than 0.5. The contribution of SOC to OC was 80.6% in PM10 and 77.7% in PM2.5, which were the highest in the summer, in accordance with the high temperature and strong solar radiation in the summer.

[Physiochemical Properties and Sources of Atmospheric Particulate Matter During Pollution Monitoring in Nanning, China].

Distribution characteristics, chemical constituents, and sources of particulate matter were measured using a scanning mobility particle sizer and single particle aerosol mass spectrometer during pollution monitoring that occurred between December 5th and December 11th, 2016, in Nanning. Results showed that particulate matter (PM) sized between 20 nm-10 µm were concentrated in the 23 to 395 nm range, with a peak of 100 nm. Three new particle types were generated during the course of this monitoring. These new 30 nm particles came into existence between 14:00 to 18:00, and grew to a size of between 40 nm and 110 nm between 20:00 to 06:00 the next day. The generation of the all three new particles was affected by motor vehicle exhaust emissions. Many secondary particles were also produced during this period of pollution. The source of the fine particulate matter was mainly from the burning of biomass, dust, and the combustion of coal. In addition, a long-distance transmission also contributed to the particles from biomass burning.

[Analysis of Chemical Composition and Pollution Source of the Fine Particulate Matter by the SPAMS in the Four Seasons in Nanning].

To study the chemical composition and pollution sources of the fine particulate matter during the four seasons in Nanning, single particle aerosol mass spectrometry was performed to characterize the fine particulate matter in Nanning during the four seasons. The correlation (R2) between the fine particulate matter number concentration and the mass concentration of the fine particulate matter obtained using SPAMS was all above 0.75 in the observation period. The particle number concentration could reflect the atmospheric pollution situation to some degree. The average mass spectrogram of the fine particulate matter reflected that secondary pollutants were more in winter and spring in Nanning. The Art-2a classification method was used to classify the chemical composition of the fine particulate matter. The results showed that the number concentration of the chemical composition and sources of pollution had differences in the four seasons. Chemical composition could reflect pollution sources. The elevated elemental carbon was positively with increasing coal combustion in winter. The elevated organic carbon was positively correlated with motor vehicle source in autumn. Rich potassium particles, levoglucosan and substance were positively correlated with biomass burning source and dust in summer. The rich sodium particles and heavy metals were higher in spring. During the process of increasing pollution, the contributions of biomass and coal combustion sources were large.

[Chemical Composition of the Single Particle Aerosol in Winter in Nanning Using SPAMS].

Single Particle Aerosol Mass Spectrometry (SPAMS) was performed to characterize the PM2.5 in Nanning from 15 to 24 February 2015. The correlation (R2) between the PM2.5 number concentration and the mass concentration of PM2.5 obtained using SPAMS was 0.76. The particle number concentration could reflect the atmospheric pollution situation to some degree. The Art-2a classification method was used to classify the chemical composition of PM2.5. The results showed that the principal chemical constituents were elemental carbon, organic elements carbon hybrid particles, organic carbon, rich potassium particles, mineral substance, rich sodium particles, second inorganic particles, levoglucosan and other heavy metals. Among them, the composition of elemental carbon was the highest, followed by organic carbon and rich potassium particles. The particle size of 80% of PM2.5 was mainly concentrated in the range of 0.2 microm to 1.0 microm with a peak value occurring at 0. 62 microm. The particle size distribution characteristics of different chemical components were similar. The number concentration of the chemical components in PM2.5 had the same variation tread with the mass concentration of PM2.5 over time. To a certain extent, the change in chemical composition could reflect the instantaneous pollution source.

[Occurrence of PFOA and PFOS in the aquatic environments and their ecological toxicities in the aquatic environments].

Based on current researches, described the sources, toxicities, analytical methods and occurrence of PFOA and PFOS in wastewater treatment plants, lakes, rivers, coastal areas and tap waters in different countries in the world. According to the limited concentrations of PFOA + PFOS in effluents of wastewater treatment plants (WTPs) put forward by Germany, the concentrations of PFOA + PFOS in WTP effluents in Singapore, Germany, Korea and England were assessed. The results showed that the concentrations of PFOA + PFOS in WTP effluents in Singapore were higher than the liminted concentration of 300 microg/L. Researches done by China, Japan, USA, and other countries showed that the concentrations of POFA and PFOS in rivers and coastal areas reached to ng/L, and the concentrations in Tennessee River, USA were the highest, reached to 100 ng/L. The risk assessments of PFOA and PFOS in tap water in some cities in China were assessed according to the risk quotients(RQ). The assessment results showed that tap waters from 19 cities in China were all below the risk level.