Site In South China Research Articles

Biota-sediment accumulation factors for Dechlorane Plus in bottom fish from an electronic waste recycling site, South China

Biota-sediment accumulation factors (BSAFs) for Dechlorane Plus (DP), a highly chlorinated flame retardant, were determined in three bottom fish species, i.e., crucian carp, mud carp, and northern snakehead from an electronic waste recycling site in South China. The average BSAFs are 0.007, 0.01, and 0.06 for syn-DP, and 0.003, 0.025, and 0.001 for anti-DP in crucian carp, mud carp, and northern snakehead, respectively, suggesting low bioaccumulation potential of DP isomers in these fish. However, the bioaccumulation factors (BAFs) determined previously in the same sample set indicated that both DP isomers were highly bioaccumulative (BAFs > 5000) in most of the samples. This implies that BSAF values may be inherently inconsistent affecting their reliability as a bioaccumulation indicator. The BSAFs for DP isomers are two orders of magnitude lower than those (average of 0.43–2.28) for extremely hydrophobic polychlorinated biphenyls (CBs 199, 203, 207 and 208), but are comparable to those (average of 0.0001–0.009) for decabromodiphenyl ether (BDE 209) determined in the same sample set. Despite of the different chemical structures of the three compound classes, significantly negative correlations between logarithm of octanol–water partition coefficients (log K OWs) and BSAFs of these chemicals were found, indicating that hydrophobicity is one of the key factors influencing the bioaccumulation of these compounds.

Dechlorane Plus (DP) in air and plants at an electronic waste (e-waste) site in South China

Air and foliage samples ( Eucalyptus spp. and Pinus massoniana Lamb.) were collected from e-waste and reference sites in South China and analyzed for Dechlorane Plus (DP) and two dechlorinated DPs. DP concentrations in the air were 13.1–1794 pg/m 3 for the e-waste site and 0.47–35.7 pg/m 3 for the reference site, suggesting the recycling of e-waste is an important source of DP to the environment. Plant DP, with concentrations of 0.45–51.9 ng/g dry weight at the e-waste site and 0.09–2.46 ng/g at the reference site, exhibited temporal patterns similar to the air DP except for pine needle at the reference site. The air-plant exchange of DP could be described with the two-compartment model. Anti-Cl 11 DP was measured in most air and plant samples from the e-waste site. The ratios of anti-Cl 11 DP to anti-DP in the air and plants may indicate the preferential uptake of dechlorinated DP by plant compared with DP.

Special Distribution of Polybrominated Diphenyl Ethers in Brain Tissues of Free-range Domestic Hens and Ducks from a Village near an Electronic Waste Recycling Site in South China

The rural village, Taizhou of Zhejiang Province, had been exposed to e-waste recycling for years, the polybrominated diphenyl ether (PBDE) levels in hens and ducks were high. The concentration of ∑PBDEs in the brain was the lowest among tissues of individual hens and ducks after correction for the respective lipid content. Also, the concentration ratio of BDE-153 versus BDE-154 (153/154) of brain was the highest among tissues of individual hens and ducks. Our results indicate that the hindrance of blood-brain barrier to compounds, such as high molecular weight and non-planar conformation (steric hindrance), contributed to the low concentration of PBDEs in the brain tissue of hens and ducks, especially in cases exposed to high levels of PBDE.

Short-range transport of contaminants released from e-waste recycling site in South China

The transport behaviors of a suite of contaminants released from electronic waste (e-waste) recycling operations, including polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), and heavy metals, were evaluated by analyzing the contaminant residues in surface soils sampled in the surrounding area of an e-waste recycling site in South China. Concentrations of PBDEs and PCBs in the soil samples ranged from 0.565 to 2908 ng g(-1) dw and from 0.267 to 1891 ng g(-1) dw, respectively, while soil residues were 0.082-2.56, 3.22-287, and 16.3-162 μg g(-1) dw for Cd, Cu, and Pb, respectively. Concentrations of PBDEs and PCBs in soil decreased with increasing distance from the source of pollution, indicating possible PBDE and PCB contamination in the surrounding areas due to the short-range transport of these compounds from the e-waste recycling site. Although no significant difference in the short-range transport potential among PBDE and PCB congeners was observed, reductions in concentrations of the highly-brominated-BDEs and highly-chlorinated-CBs were slightly quicker than those of their less-halogen-substituted counterparts. Conversely, heavy metals showed the lowest transport potential due to their low vapor pressure, and results showed metals would remain near the pollution source instead of diffusing into the surrounding areas. Finally, mass inventories in areas near the e-waste site were 0.920, 0.134, 0.860, 4.68, 757, and 673 tons for BDE209, PBDEs (excluding BDE209), PCBs, Cd, Cu, and Pb, respectively.

Polycyclic aromatic hydrocarbons with molecular weight 302 in PM2.5 at two industrial sites in South China

Daytime and nighttime PM(2.5) samples were collected between August 5 and 16, 2009 and between January 24 and February 4, 2010 in an industrial complex site (site A) and an electronic waste recycling site (site B) to determine the seasonal and diurnal variations of 19 individual polycyclic aromatic hydrocarbons (PAHs) with molecular weight 302 (MW302) including four highly carcinogenic dibenzopyrene (DBP) isomers dibenzo[a,l]pyrene (DBalP), dibenzo[a,e]pyrene (DBaeP), dibenzo[a,i]pyrene (DBaiP), and dibenzo[a,h]pyrene (DBahP). This is the first report on DBP isomers in air particles from South China. The total concentration of PAH MW302 isomers ranged from 1.65 to 3.60 ng m(-3) in summer and 3.82 to 9.81 ng m(-3) in winter. The strongest peaks in the chromatograms of the MW302 isomers were naphtha[2,1-a]pyrene (N21aP), dibenzo[j,l]fluoranthene (DBjlF), naphtha[1,2-b]fluoranthene (N12bF), naphtha[1,2-k]fluoranthene (N12kF) and dibenzo[a,e]fluoranthene (DBaeF), constituting 52.0 to 55.4% of the total MW302 isomers. All the MW302 isomers showed notable seasonal variations. Most of the MW302 isomers in site B showed distinctive diurnal variations with higher concentrations occurring in the night. Taking into account both concentration and potency equivalence factors (PEFs), the strongest carcinogen in the analyzed samples was DBaiP, and the ratios of sum carcinogenic potency of four highly carcinogenic DBP isomers to benzo[a]pyrene (BaP) was about 0.94 in winter to 1.89 in summer, indicating the importance of DBP isomers for the risk assessment. Health risk assessment indicated that on average, 1 in 100 000 residents in the two industrial sites may have an increased risk of cancer due to PAH exposure.

Several current-use, non-PBDE brominated flame retardants are highly bioaccumulative: Evidence from field determined bioaccumulation factors

With the phaseout of brominated flame retardants (BFRs) polybrominated diphenyl ethers (PBDEs), some non-PBDE BFRs have prompted to be alternatives to the discontinued PBDEs. To assess the bioaccumulation potential of these chemicals, field bioaccumulation factors (BAFs) for several non-PBDE BFRs including hexabromocyclododecanes (HBCDs), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), pentabromotoluene (PBT), pentabromoethylbenzene (PBEB), and hexabromobenzene (HBB), were determined in the aquatic species from a natural pond in an electronic waste recycling site in South China. The log BAFs ranged 2.58–6.01, 3.24–5.58, 3.44–5.98, 2.85–5.98, 3.32–6.08, 2.04–4.77, 2.72–4.09 and 3.31–5.54 for α-HBCD, β-HBCD, γ-HBCD, ∑ HBCDs, BTBPE, PBT, PBEB, and HBB, respectively. The log BAF values for HBCD isomers, BTBPE, and HBB were greater than 3.7 (corresponding BAF value 5000) in most of the investigated species, demonstrating their highly bioaccumulative properties. α-, β-, and γ-HBCDs, BTBPE, and HBB appeared comparable or had even greater BAFs compared to PBDE congeners with similar K OW, suggesting that these BFRs may have a potentially high environmental risk. The BAFs for the given BFR compound were largely variable between species, due to the species-specific feeding ecology, trophic level, and metabolic capacity for these pollutants. Positive linear relationships between log BAF and log K OW ( r 2 = 0.59, p = 0.04), and molecular weight ( r 2 = 0.54, p = 0.06) of non-PBDE BFRs were observed in the species with low trophic level (Chinese mysterysnail), suggesting that the chemical's physicochemical properties also played key roles in the bioaccumulation processes.

Early Pottery in South China

Potsherds of thick walls with coarse inclusions have been found in several archaeological sites in South China, associated with flaked or ground stone tools and ground organic implements. This paper focuses on the natural and cultural contexts, the chronology, and the characteristics of the early pottery found in South China, as well as the impetus to the origin of pottery and several related issues. It is argued that the earliest potters in South China were affluent foragers, who lived on diversified natural resources and were members of egalitarian societies. The earliest pottery in this region is tentatively dated to approximately 12,000 years ago, characterized by thick, crumbled walls built by hand pinching and without decoration. Although potsherds found in South China may not be the earliest in terms of the absolute dates, they represent the very beginning of pottery manufacturing as a technological invention from the terminal Pleistocene to the early Holocene in southern East Asia. Based on current archaeological data and the results of multi-disciplinary analyses, it is argued that South China seems to have been an area for the origin of pottery, which might have been associated with subsistence strategy changes. Furthermore, there might have been cultural exchanges between the prehistoric potters in South China and those in adjacent areas.

Tissue Distribution of Polybrominated Diphenyl Ethers (PBDEs) in Captive Domestic Pigs, Sus scrofa, from a Village Near an Electronic Waste Recycling Site in South China

The dominant part of PBDEs residue in pig tissues was BDE-47 accounted for 48.2% approximately 66.9%, followed by BDE-99 from 15.9% to 24.2%. When the data were on lipid weight basis, the summation operatorPBDEs concentrations in tissues of individual pig showed the same order of liver > muscle, intestine > fat. Principal component analysis and PBDE congener mean concentration ratios of muscle versus liver (M/L), fat versus liver (F/L) and intestine versus liver (I/L) showed the higher accumulation ability of PBDEs in liver than in other tissues. And the PBDE mean concentration ratios of M/L, F/L and I/L had the trend of decrease with increasing bromination degree of PBDE congeners.

Abundance and size distribution of HULIS in ambient aerosols at a rural site in South China

HUmic-LIke Substances (HULIS) comprise a significant fraction of the water-soluble organic aerosol mass and influence the water uptake properties of aerosols in the atmosphere. In this work, the abundance and size distributions of HULIS in ambient aerosols were measured in a rural location in South China at a time with a visible presence of crop residue burning. PM 2.5 samples of fresh smoke from burning rice straw and sugar cane leaves were also collected and analyzed for HULIS and major aerosol constituents. HULIS were abundant in both ambient samples and in fresh biomass burning emissions, accounting for ∼60% of the water-soluble organic carbon in the ambient aerosols and ∼30% in the fresh biomass burning aerosols. In the particles in the range of 0.32–1.8 μm, the abundance of HULIS was 40–90% of the combined abundance of sulfate and ammonium, suggesting that HULIS should be considered when quantifying the role of sulfate aerosols serving as cloud condensation nuclei. The size distribution of HULIS was characterized by a dominant droplet mode with a mass median aerodynamic diameter (MMAD) in the range of 0.63–0.87 μm, accounting for 81% of the total HULIS mass, a minor condensation mode (12%, MMAD: 0.23–0.28 μm) and a coarse mode (7%, MMAD: 4.0–5.7 μm). The small amount of HULIS in the coarse mode indicated that soil-derived HULIS was a very minor source. On the basis of the size distribution characteristics, HULIS were postulated to have multiple sources, including secondary formation in cloud droplets, secondary formation through heterogeneous reactions or aerosol-phase reactions, and primary emissions from biomass burning.

Residues of Polybrominated Diphenyl Ethers in Frogs (Rana limnocharis) from a Contaminated Site, South China: Tissue Distribution, Biomagnification, and Maternal Transfer

Environmental pollutants are suspected to be a cause of global declines in amphibian populations, but few data are available on the bioaccumulation of polybrominated diphenyl ethers (PBDEs) in amphibians. To examine the tissue distribution, biomagnification potential, and maternal transfer of PBDEs in frogs, eighteen PBDE congeners were measured in the muscle, liver, and egg tissues of rice frogs (Rana limnocharis) and insects collected from an electronic waste (e-waste) recycling site in South China. PBDE levels in the frogs ranged from 0.63 to 11.6, 4.57 to 56.2, and 10.7 to 125 ng/g wet wt in the muscles, livers, and eggs, respectively. The frogs exhibited a unique congener profile, compared to those in aquatic and terrestrial species, with BDEs 99, 153, 183, 209, and 47 as the dominant congeners, intermediating between aquatic and terrestrial species. Most of the PBDE congeners in general showed higher affinity to liver than to muscle tissue. Except for BDEs 28, 47, 66, 138, and 206, the average biomagnification factors (BMFs) for all PBDE congeners were greater than 1.0, providing clear evidence of their biomagnification from insects to frogs. A parabolic relationship between log BMFs and bromine atom numbers or log Kow of PBDEs was observed, with the maximum BMF values for PBDEs with 6 bromine atoms (or at a log K(ow) of approximately 8.0). Relatively higher levels of 3-MeO-BDE 47 were found in male frogs, suggesting that male frogs in the present study might have higher metabolic capacity for PBDEs compared to female frogs. The ratio of levels in egg/female liver, indicating mother-to-egg transfer capacity, increased with increasing bromine atom numbers up to 7 and then declined as the bromine atom numbers rose. This indicated that the physicochemical properties of the congeners (e.g., K(ow), molecular sizes, and structures), resulting in different affinities to transport proteins, might impact their maternal transfer in frogs.

Carbon isotope analysis for source identification of atmospheric formaldehyde and acetaldehyde in Dinghushan Biosphere Reserve in South China

Formaldehyde and acetaldehyde are two most abundant carbonyls in ambient air. Biogenic emission has been proposed as a significant source other than anthropogenic emissions and atmospheric secondary formation. Here at a forest site in South China, the carbon isotopic compositions of formaldehyde and acetaldehyde emitted from leaves of three tree species ( Litsea rotundifolia, Canarium album and Castanea henryi) were measured in comparison with the bulk carbon isotopic compositions of tree leaves. δ 13C data of the emitted aldehydes (from −31‰ to −46‰) were quite different for tree species, which were all more depleted in 13C than the tree-leaf bulk δ 13C values (from −27‰ to −32‰). Formaldehyde in ambient air at the forest site had δ 13C values different from those of leaf-emitted formaldehyde, indicating other sources for ambient formaldehyde apart from direct emission from leaves, most probably the photooxidation of biogenic hydrocarbon like isoprene and monoterpene. The δ 13C differences of acetaldehyde between ambient data and those of tree leaves emission were less than 1‰, implying direct biogenic emission as the dominant source.

Polybrominated diphenyl ethers (PBDEs) in free-range domestic fowl from an e-waste recycling site in South China: Levels, profile and human dietary exposure

To evaluate the status of polybrominated diphenyl ethers (PBDEs) contamination in poultry and sequentially human exposure through consumption of poultry in an e-waste recycling site in South China, two kinds of free-range domestic birds, chicken and duck, were collected and their muscle and liver tissues were analyzed for 16 PBDE congeners. Chicken shows higher PBDE concentrations (summation of 16 PBDE congeners) in both muscle and liver tissues, ranged from 5.7 to 4381 and from 1.5 to 7897 ng/g (lipid weight, the same hereinafter), respectively, compared to duck, ranged from 2.4 to 51 and from 1.9 to 134 ng/g. Different living habitat and feeding habits between the two species might be responsible for this observation. No sex-related differences in PBDE concentrations were found for the two species, while the PBDE concentrations in muscle were higher than those in liver for chicken. The PBDE concentrations in muscle of chicken in the present study were higher than the levels of PBDEs in chicken from other studies reported by far. BDE209 and nona-BDEs were the major congeners in poultry. Comparison of PBDE profiles between birds and environmental matrix implied that the biodebromination of BDE209 might occur in poultry. The intake of PBDEs through consumption of poultry ranges from 7.8 ng/day to 3582 ng/day with a medial 68 ng/day, which is comparable to the calculated values through consumption of all foodstuffs in other studies. The present study suggested that the total dietary PBDEs intake for local residents might be considerably enhanced due to the e-waste recycling activity.

Stratégie de débitage et mode de façonnage des industries du Paléolithique inférieur en Chine et en Europe entre 1 Ma et 400 000 ans: Ressemblances et différences de la culture de l’homme de Yunxian et Acheuléen européen

These stone tools from Yunxian with other Lower Paleolithic sites in South China, for example, the site Lantian (Shanxi, China) and the site Bose (Guangxi, China), indicates that there are many common characteristics among these industries. There are choppers, chopping-tools, picks, hand-axes, cleavers and scrapers. Long ago we thought that there are not hand-axes in China. In fact, there are lots of hand-axes in China and these hand-axes existed more earlier than those in Europe. The hand-axe appeared in China before 800,000 years old and it barely arrived in Europe before 600,000 years old. The quaternary deposits of the site of Yunxian Hominid (Hubei, China) are at least dated to 800,000 years old. A large quantity of lower Paleolithic material was discovered. The types of the tools are choppers, picks, scrapers, hand-axes and cleavers. The pebbles tools make up the majority of the implements. Small flake tools are relatively rare. The lithic industries comparison of the two regions has help us to know the cultural evolution in China and Europe.

Bioaccumulation of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) in wild aquatic species from an electronic waste (e-waste) recycling site in South China

Water and several wild aquatic species including Chinese mysterysnail, prawn, fish, and water snake were collected from a reservoir surrounded by several e-waste recycling workshops in South China. The samples were examined to investigate the levels and bioaccumulation extent of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) released from electronic waste (e-waste) which was processed by crude recycling method. Elevated levels of PBDEs [52.7 to 1702 ng/g wet weight (ww)] and PCBs (20.2–25958 ng/g ww) were found in the collected biota species compared to that in the reference samples (13.0–20.5 ng/g ww for PBDEs and 75.4–82.8 ng/g ww for PCBs). log BAF (bioaccumulation factor) ranged from 2.9 to 5.3 for PBDEs and from 1.2 to 8.4 for PCBs, depending on congeners and species. The relationship between log BAFs and log K OW (octanol–water partition coefficient) can be adequately described by species-specific parabolic models wherein log BAFs generally increased at log K OW < 7 then decreased with further increasing log K OW both for PBDEs and PCBs. The exceptions were for Chinese mysterysnail and prawn, in which the log BAFs showed a positive linear correlation with log K OW for PBDEs. Some PBDE and PCB congeners showed BAF values declining from the general trend predicted by K OW, largely attributing to metabolism of these congeners in species sampled.

New Thinking on Flame Retardants

No one wants their bed, couch, chair, computer, or TV to catch on fire. “If an ordinary upholstered chair in your home gets ignited, it can essentially take your whole house down,” says Richard Gann, a senior research scientist at the U.S. National Institute of Standards and Technology’s (NIST) Building and Fire Research Laboratory. The most flammable part of a mattress or couch is its plastic polyurethane foam cushioning, he explains. Once a fire gets through a chair or mattress’s fabric covering and into this cushioning, it can start a catastrophic reaction that quickly leads to “flashover,” in which nearly everything combustible inside a room ignites simultaneously. Until very recently, brominated flame retardants, especially polybrominated diphenyl ethers (PBDEs), were one of the main materials used to reduce the speed with which the plastic components of consumer goods including beds, couches, chairs, and electronics could be consumed by fire. However, growing evidence shows that PBDE compounds are escaping from the products they protect and making their way into the products’ users. Moreover, the chemicals may disrupt human thyroid hormone functioning and cause other health effects, prompting many nations to ban or suspend their use in new consumer goods. [For more information on the health effects of PBDEs, see “Unwelcome Guest: PBDEs in Indoor Dust, p. A202 this issue.] Although bromine- and chlorine-containing flame retardants are still used in some products, the need for new alternatives is being driven by a confluence of policy, standards, and pressure from environmental groups. Europe banned the use of two formulations, PBDE pentaBDE and octaBDE, in 2004, the same year they were withdrawn from the North American market. A third compound, decaBDE, was banned 1 April 2008 by the European Court of Justice. Stateside, Maine has banned the use of decaBDE, the only PBDE still on the market in North America, in mattresses and residential upholstered furniture produced and sold in that state, and will extend the ban to electronics in 2010. Washington prohibits the use of decaBDE in mattresses and sets a process for a future ban in furniture and electronics if the state can identify a safer and feasible alternative that meets fire safety standards. Asian countries and other U.S. states have similar legislation in the works. “Instead of adding new fire retardant chemicals that ultimately may be shown to cause health problems, we should be asking whether we need to use these chemicals or if there are other ways to achieve equivalent fire safety,” contends Arlene Blum, a biophysical chemist and visiting scholar at the University of California, Berkeley. “So many of the chemicals we have banned in the past were flame retardants—think about asbestos, polychlorinated biphenyls, polybrominated biphenyls, tris(2,3-dibromopropyl) phosphate, PBDEs—[and] they all ended up in the environment and in people,” she points out. “We need to think carefully about adding these sorts of chemicals to consumer products before there is adequate health information.”

Characteristics and diurnal variations of NMHCs at urban, suburban, and rural sites in the Pearl River Delta and a remote site in South China

The Pearl River Delta (PRD) is one of the most industrialized and urbanized regions in China. With rapid growth of the economy, it is suffering from deteriorating air quality. Non-methane hydrocarbons (NMHCs) were investigated at urban and suburban sites in Guangzhou (GZ), a rural site in PRD and a clean remote site in South China, in April 2005. Additional roadside samples in GZ and Qingxi (QX, a small industrial town in PRD), ambient air samples at the rooftop of a printing factory in QX and exhaust samples from liquefied petroleum gas (LPG)—fueled taxis in GZ were collected to help identify the source signatures of NMHCs. A large fraction of propane (47%) was found in exhaust samples from LPG-fueled taxis in GZ and extremely high levels of toluene (2.0–3.1 ppmv) were found at the rooftop of the printing factory in QX. Vehicular and industrial emissions were the main sources of NMHCs. The effect of vehicular emission on the ambient air varied among the three PRD sites. The impact of industrial emissions was widespread and they contributed greatly to the high levels of aromatic hydrocarbons, especially toluene, at the three PRD sites investigated. Leakage from vehicles fueled by LPG contributed mainly to the high levels of propane and n-butane at the urban GZ site. Ethane and ethyne from long-range transport and isoprene from local biogenic emission were the main contributors to the total hydrocarbons at the remote site. Diurnal variations of NMHCs showed that the contribution from vehicular emissions varied with traffic conditions and were more influenced by fresh emissions at the urban site and by aged air at the suburban and rural sites. Isoprene from biogenic emission contributed largely to the ozone formation potential (OFP) at the remote site. Ethene, toluene and m/ p-xylene were the main contributors to the OFP at the three PRD sites.

Plant Response to Metal Contamination at an Oil Shale Tailing Site in Maoming, South China

AbstractThe performance of phytoextraction is evaluated at an oil shale tailing site in South China, where the soil is moderately contaminated with heavy metals. Soil, wastes, and plant tissues (leaf, stem, and root) were collected from the site and analyzed for metals. The analytical results show that the plants can extract more metal from the surrounding soil than their nutrient requirements. Though the plants sampled are not hyperaccumulators for heavy metals as defined by other researchers, they can translocate heavy metals to their leaves and tolerate acidic soil with pH as low as 3.4. This makes them candidates for contaminated site remediation. Abelmoschus moschatus, Eleocharis quisetina J. et C.Presl, Acacia confusa wild., and Eucalyptus saligna were particularly effective in translocating heavy metals to easily harvestable leaves and shoots.

Atmospheric deposition of nitrogen at five subtropical forested sites in South China

Elevated concentrations of reactive nitrogen (N) in precipitation have been reported for many cities in China. Due to increased use of fossil fuels and expansion in agriculture, further increases in deposition of ammonia (NHx) and reactive N oxides (NOy) are predicted. Increased deposition of reactive N is likely to affect N dynamics and N runoff in forest ecosystems. Yet, in China little work has been done to quantify the levels of atmospheric N deposition in such systems. Here, we assess the deposition of inorganic N (ammonium, NH4+ and nitrate, NO3-) for five subtropical forest ecosystems in remote and urban areas of South China. Annual volume-weighted concentrations in bulk precipitation range from 0.18 to 1.55 mg NH4+ -N L(-1) and from 0.12 to 0.74 mg NO3- -N L(-1). These values are large and several times greater than those reported for remote sites of the world. The fluxes of total inorganic N (TIN) in wet-only deposition range from 0.8 to 2.3 g N m(-2) yr(-1), with NH4+ -N contributing 54% to 77%. Both the tree canopy and the ground vegetation layer are important in determining the net N flux reaching the forest floor, but the net effect varies from site to site. At TieShanPing (TSP), close to Chongqing city, and at CaiJiaTang (CJT), near Shaoshan (Hunan province), the canopy represents a net source of N, probably due to dry deposition. At the other three sites (LiuChongGuan (LCG), LeiGongShan (LGS), both in Guizhou province, and LiuXiHe (LXH) in Guangdong), a net loss of reactive N from precipitation water occurs in the canopy, probably due to uptake processes. The total annual atmospheric TIN load is estimated to range from at least 0.8 g N m(-2) yr(-1) to 4.0 g N m(-2) yr(-1), with a considerable contribution from dry deposition. Concentrations and fluxes of inorganic N in tree canopy throughfall are greater than those in North America. Also the contribution of NH4+ -N to TIN fluxes in throughfall (40% to 70%) is greater than in North America. Our sites have N deposition levels and NH4+ -N contributions similar to those found in Northwest and central Europe. The TIN loads at TSP and CJT far exceed 2.5 g N m(-2) yr(-1), which is the N deposition load above which NO3- leaching is expected in temperate and boreal forests.

Platinum concentrations in ambient aerosol at a coastal site in South China

Abstract With the burgeoning vehicle ownership in China, the emissions of certain trace pollutants are becoming more widespread and of more concern. We present results from the first measurements of platinum in airborne total suspended particulate matter (TSP) at a suburban (CityU) and a roadside (MK) sampling site in southern China at Hong Kong. TSP samples were taken with high volume air samplers at these sites with low and high traffic density, respectively, on a 2-day basis and were analyzed by inductively coupled plasma—dynamic reaction cell—mass spectrometry (ICP-DRC-MS). The results are similar from the use of two different isotopes: 194 and 195. The 48-h average Pt concentrations were 8.8 pg m−3 at CityU and 24.1 pg m−3 at MK, being higher at the site with greater traffic density, and were in the range from 6 to 38 pg m−3. The airborne Pt was found to be significantly correlated with vehicle tracer species (Zr and Ce) as well as with NO and NOx. The ratio Ce/Zr was the same at both sites whereas the ratios Pt/Zr and Pt/Ce were about 20% greater at the MK site, showing the different mobility of Pt, attributed to chemical and/or particle size effects.

Relationships of trace gases and aerosols and the emission characteristics at Lin'an, a rural site in eastern China, during spring 2001

We present measurements of trace gases and fine aerosols obtained from a rural site in eastern China during 18 February to 30 April 2001. The field program aimed to characterize the variations in aerosol and gaseous pollutant concentrations and the emission signatures from the inland region of eastern China in the spring season. The data included O3, CO, NO, NOy*, SO2, methane, C2‐C8 nonmethane hydrocarbons (NMHCs), C1‐C2 halocarbons, and the chemical composition of PM2.5. The average hourly mixing ratios (±standard deviation) of CO, SO2, and NOy* were 677 (±315) ppbv, 15.9 (±14.6) ppbv, and 13.8 (±7.2) ppbv, respectively. The mean daytime ozone mixing ratio was 41 (±19) ppbv. The most abundant NMHC was ethane (3189 ± 717 pptv), followed by ethyne (2475 ± 1395 pptv), ethene (1679 ± 1455 pptv), and toluene (1529 ± 1608 pptv). Methyl chloride was the most abundant halocarbon (1108 ± 653 pptv). The average concentrations of particulate organic matter (POM, as organic carbon, OC, times 1.4) and elemental carbon (EC) in PM2.5 were 21.5 (±7) μg/m3 and 2.5 (±0.7) μg/m3, respectively, and sulfate and nitrate levels were 17.3 (±6.6) and 6.5 (±4) μg/m3, respectively. CO showed moderate to good correlation with NOy* (r2 = 0.59), OC (r2 = 0.65), CH3Cl (r2 = 0.59), soluble potassium (r2 = 0.53), and many NMHCs, indicating contributions from the burning of biofuel/biomass. CO also correlated with an industrial tracer, C2Cl4, indicative of some influence from industrial sources. SO2, on the other hand, correlated well with EC (r2 = 0.56), reflecting the contribution from the burning of coal. Ammonium was sufficiently abundant to fully neutralize sulfate and nitrate, indicating that there were strong emissions of ammonia from agricultural activities. Silicon and calcium had poor correlations with iron and aluminum, revealing the presence of source(s) for Si and Ca other than from soil. Examination of C2H2/CO, C3H8/C2H6, nitrate/(nitrate + NOy*), and sulfate/(SO2 + sulfate) suggested that relatively fresh air masses had been sampled at the study site in the spring season. Comparison of the observed ratios/slopes with those derived from emission inventories showed that while the observed SO2/NOy* ratio (1.29 ppbv/ppbv) in March was comparable (within 20%) to the inventory‐derived ratio for the study region, the measured CO/NOy* slope (37 ppbv/ppbv) was about 200% larger. The observed slope of CO relative to NMHC (including ethane, propane, butanes, ethene, and ethyne) also indicated the presence of excess CO, compared to the ratios from the inventories. These results strongly suggest that emissions of CO in eastern China have been underrepresented. The findings of this study highlight the importance of characterizing trace gases and aerosols within source regions of the Asian continent. The springtime results were also compared with data previously collected at the site in 1999–2000 and with those obtained on the Transport and Chemical Evolution over the Pacific (TRACE‐P) aircraft and from a coastal site in South China for the same study period.