Zhenchuan Niu

Characterization of polybrominated diphenyl ethers (PBDEs) and hydroxylated and methoxylated PBDEs in soils and plants from an e-waste area, China.

In order to characterize polybrominated diphenyl ethers (PBDEs), and hydroxylated and methoxylated PBDEs (OH-PBDEs and MeO-PBDEs) in the soil-plant system, soil and plant samples were collected from an e-waste recycling area in China. Forty one PBDEs, twelve OH-PBDEs and MeO-PBDEs were detected in the soil and plant samples. Concentrations of PBDEs in roots were significantly correlated to their concentrations in the soils, but the percentages of lower brominated congeners in the plants were higher than those in the soils. Significant positive linear relationships exist between concentrations of ∑OH-PBDEs and ∑MeO-PBDEs with higher levels of ∑MeO-PBDEs than those of ∑OH-PBDEs in the soils, plant roots and leaves. A majority of the OH-/MeO-PBDEs had the hydroxyl or methoxy group at the ortho-positions to the biphenyl bond for most of the plant species. However the occurrence of meta- and para- substituted OH-/MeO-PBDEs in soils and plants were also confirmed.

Characteristics and sources of atmospheric mercury speciation in a coastal city, Xiamen, China

Semi-continental monitoring of gaseous elemental mercury (GEM), particulate mercury (Hgp), and reactive gaseous mercury (RGM) was conducted in the Institute of Urban Environment, CAS in Xiamen, China from March 2012 to February 2013. The average concentrations and relative standard deviations (RSD) were 3.50 (34.6%) ng m(-3), 174.41 (160.9%) pg m(-3), and 61.05 (113.7%) pg m(-3) for GEM, Hgp, and RGM, respectively. The higher concentrations of GEM and Hgp were observed in spring and winter months, indicating the combustion source, while RGM showed the different seasonal variation with highest concentration in spring and the minimum value in winter. The concentrations of Hg species were generally elevated in nighttime and low in daytime to reflect the diurnal changes in meteorology, especially the mixing condition of the air masses. The high Hg concentrations were observed in SWW-NW sectors due to calm wind while the low levels in NE-SE due to high speed wind, and the amplitude was much larger for Hgp and RGM. Backward trajectories calculation indicated that summer air masses were much more from ocean with lower Hg while the air masses were mainly from inland area in other seasons. Principal component analysis suggested that combustion and road traffic emissions were the dominant anthropogenic mercury sources for the study area, and the temporal distribution of atmospheric mercury was mainly the result of climatological change.

Spatial distribution and sources identification of elements in PM2.5 among the coastal city group in the Western Taiwan Strait region, China

The main purpose of this study was to investigate the spatial variations of 20 elements (Al, Si, Ti, Ca, Fe, Mg, Cr, Mn, Ni, P, S, K, Cu, Cl, V, Se, Br, As, Zn, and Pb) in PM(2.5) (particle matters ≤ 2.5 μm in aerodynamic diameter) in the coastal city group in the Western Taiwan Strait (WTS) region, China during spring 2011. The average PM(2.5) mass concentration at 13 sites was 77.0 μg/m(3) and the elemental fraction accounted for about 10-20%. Multivariate analyses (principal component analysis and cluster analysis) and a correlation matrix were used to identify the sources of elements in PM(2.5). The results revealed that the elements originated mainly from traffic emissions, coal combustion, pyrometallurgical processes, and crustal sources. Spatially, the concentrations of elements were generally higher in several rapidly growing locations, and the enrichment factors (EFs) for most elements were much higher at the northern sites than those at the southern sites, suggesting that the air quality in the northern part of the study area was strongly affected by anthropogenic activity. Backward wind trajectory analysis during the sampling period indicated that the concentrations of elements in PM(2.5) in the WTS region were greatly impacted by dust particles transported from Northern China in spring.

Source contributions to carbonaceous species in PM2.5 and their uncertainty analysis at typical urban, peri-urban and background sites in southeast China.

Determination of (14)C and levoglucosan can provide insights into the quantification of source contributions to carbonaceous aerosols, yet there is still uncertainty on the partitioning of organic carbon (OC) into biomass burning OC (OCbb) and biogenic emission OC (OCbio). Carbonaceous species, levoglucosan and (14)C in PM2.5 were measured at three types of site in southeast China combined with Latin hypercube sampling, with the objectives to study source contributions to total carbon (TC) and their uncertainties, and to evaluate the influence of levoglucosan/OCbb ratios on OCbb and OCbio partitioning. It was found reliably that fossil fuel combustion is the main contributor (62.90-72.23%) to TC at urban and peri-urban sites. Biogenic emissions have important contribution (winter, 52.98%; summer, 45.71%) to TC at background site. With the increase in levoglucosan/OCbb ratios, the contribution of OCbio is increased while OCbb is decreased in a pattern of approximate natural logarithm at a given range.

Field controlled experiments of mercury accumulation in crops from air and soil

Field open top chambers (OTCs) and soil mercury (Hg) enriched experiments were employed to study the influence of Hg concentrations in air and soil on the Hg accumulation in the organs of maize (Zea mays L.) and wheat (Triticum aestivum L.). Results showed that Hg concentrations in foliages were correlated significantly (p < 0.05) with air Hg concentrations but insignificantly correlated with soil Hg concentrations, indicating that Hg in crop foliages was mainly from air. Hg concentrations in roots were generally correlated with soil Hg concentrations (p < 0.05) but insignificantly correlated with air Hg concentrations, indicating that Hg in crop roots was mainly from soil. No significant correlations were found between Hg concentrations in stems and those in air and soil. However, Hg concentrations in upper stems were usually higher than those in bottom stems, implying air Hg might have stronger influence than soil Hg on stem Hg accumulation.

Characterization of mercury in atmospheric particulate matter in the southeast coastal cities of China

Although present in a low concentration in the atmosphere, mercury in particulate matter (PHg) plays an important role in the biogeochemical process of mercury. In this study, the mercury concentrations in three size fractions of airborne particulate matters collected from 14 sites (12 urban sites, 1 rural site and 1 remote site) in the southeast coastal cities of China during different seasons in 2010–2011 were investigated. Most of PHg (46.8–71.9%) was concentrated in the finer particles, i.e. PM2.5 (particulate matter ≤2.5 µm in aerodynamic diameter). The average mercury concentrations in PM2.5 were 141.2±128.1 (range of 7.6–956.5), 37.0±19.2 (5.6–89.4), and 24.0±14.6 (3.2– 59.9) pg m–3 at urban, rural, and remote sites during the whole sampling period, respectively. The PHg concentrations were almost at the same level in spring, autumn, and winter, approximately two times of that in summer. PHg concentrations in the atmosphere displayed a significant spatial variation with far higher values in urban areas than those at rural and remote sites. The dry deposition fluxes of total PHg estimated by a theoretical model were 38.3, 47.7, and 58.7 µg m–2 y–1 at Ji’an (JA), Jimei (JM), and Longwen (LW), respectively. The backward air trajectory analysis revealed that the atmospheric PHg concentrations were mainly influenced by air masses from ocean sources that diluted PHg in summer and on contrary from continental sources in other seasons.

Mercury in leaf litter in typical suburban and urban broadleaf forests in China

To study the role of leaf litter in the mercury (Hg) cycle in suburban broadleaf forests and the distribution of Hg in urban forests, we collected leaf litter and soil from suburban evergreen and deciduous broadleaf forests and from urban forests in Beijing. The Hg concentrations in leaf litter from the suburban forests varied from 8.3 to 205.0 ng/g, with an average (avg) of (49.7 +/- 36.9) ng/g. The average Hg concentration in evergreen broadleaf forest leaf litter (50.8 + 39.4) ng/g was higher than that in deciduous broadleaf forest leaf litter (25.8 +/- 10.1) ng/g. The estimated Hg fluxes of leaf litter in suburban evergreen and deciduous broadleaf forests were 179.0 and 83.7 mg/(ha x yr), respectively. The Hg concentration in organic horizons (O horizons) ((263.1 +/- 237.2) ng/g) was higher than that in eluvial horizons (A horizons) ((83.9 +/- 52.0) ng/g). These results indicated that leaf litterfall plays an important role in transporting atmospheric mercury to soil in suburban forests. For urban forests in Beijing, the Hg concentrations in leaf litter ranged from 8.8-119.0 (avg 28.1 +/- 16.6) ng/g, with higher concentrations at urban sites than at suburban sites for each tree. The Hg concentrations in surface soil in Beijing were 32.0-25300.0 ng/g and increased from suburban sites to urban sites, with the highest value from Jingshan (JS) Park at the centre of Beijing. Therefore, the distribution of Hg in Beijing urban forests appeared to be strongly influenced by anthropogenic activities.

Atmospheric Fossil Fuel CO2 Traced by Δ14C in Beijing and Xiamen, China: Temporal Variations, Inland/Coastal Differences and Influencing Factors

One year of atmospheric Δ(14)CO2 were observed in 2014 in the inland city of Beijing and coastal city of Xiamen, China, to trace temporal CO2ff variations and to determine the factors influencing them. The average CO2ff concentrations at the sampling sites in Beijing and Xiamen were 39.7 ± 36.1 ppm and 13.6 ± 12.3 ppm, respectively. These contributed 75.2 ± 14.6% and 59.1 ± 26.8% to their respective annual ΔCO2 offsets over background CO2 concentrations. Significantly (p < 0.05) high CO2ff values were observed in winter in Beijing. We did not find any significant differences in CO2ff values between weekdays and weekends. Diurnal CO2ff variations were plainly evident, with high values between midnight and 4:00, and during morning and afternoon rush hours. The sampling site in the inland city of Beijing displayed much higher CO2ff inputs and overall temporal variations than the site in the coastal city of Xiamen. The variations of CO2ff at both sites were controlled by a combination of emission sources, topography, and atmospheric dispersion. In particular, diurnal observations at the urban site in Beijing showed that CO2ff was easily accumulated under the southeast wind conditions.

Pollution characteristics of volatile organic compounds in the atmosphere of Haicang District in Xiamen City, Southeast China

The compositions, spatial distributions, seasonal variations and ozone formation potential (OFP) of volatile organic compounds (VOCs) were investigated in the atmosphere of Haicang District, Xiamen City, Southeast China. Twenty-four types of VOCs were measured in this study, and ethanol, methylene chloride, toluene, ethyl acetate and isopropyl alcohol were the abundant species based on concentration rank. The concentrations of total VOCs (TVOCs) in industrial areas were higher than those in residential and administrative areas and background site. For industrial areas, the TVOCs concentrations in summer were higher than those in winter, which might result from higher emissions from industrial activities because of stronger evaporation in summer. In contrast, non-industrial areas showed higher concentrations in winter due to the unfavorable meteorological conditions. The spatial distribution of BTEX (benzene, toluene, ethylbenzene and xylene) followed the order of industrial areas > residential and administrative areas > background site, and the concentrations in summer were lower than those in winter for most sites. The high ratios (8.9-14.0) of T/B in this study indicated that industrial emissions were the main sources in this district. X/B ratios were used to assess the ages of air parcels and provided evidence of the transport of air parcels among these sites. Total OFP (TOFP) showed the trend of increase with the increase of TVOCs, and toluene was found as the major contributor to TOFP.

Application of the Environmental Internet of Things on monitoring PM2.5 at a coastal site in the urbanizing region of southeast China

Particulate matter pollution, nowadays, is one of the most concerning environmental problems in Chinese cities, and yet monitoring of PM2.5 (aerodynamic diameter of particle ≤2.5 μm) by means of Environmental Internet of Things (EIoT) is still limited in the urbanizing regions in China. A real-time 1 year continuous observation of PM2.5 by EIoT was carried out at a coastal site in Xiamen City during 2012, with the objective to explore the temporal variations and possible sources of PM2.5 in this urbanizing region. The annual average PM2.5 mass concentration was 32.7 ± 9.6 μg m−3, with the highest level in spring (43.6 ± 5.0 μg m−3) and lowest in summer (21.0 ± 2.5 μg m−3). The mean diurnal pattern of PM2.5 mass concentrations had an obvious morning peak and low values from midnight to dawn. Additionally, the concentrations on workdays were clearly higher in contrast to those on weekends. These results indicate that particulate matter in this region is mainly influenced by anthropogenic activities, and could be effectively scavenged by precipitation. Pollution rise suggested that particulate matters were mainly from civil engineering during the construction of new urban area. A distinct characteristic of particulate matters in this urbanizing region was the low ratio (0.40) of PM2.5/PM10, which might result from the increment of coarse particles emission from freeways, construction, and sea spray. The outcomes also show that EIoT technology is convenient for the management of particulate matter pollution.