Contamination assessment of arsenic and heavy metals in a typical abandoned estuary wetland—a case study of the Yellow River Delta Natural Reserve

Coastal and estuarine areas are often polluted by heavy metals that result from industrial production and agricultural activities. In this study, we investigated the concentration trait and vertical pattern of trace elements, such as As, Cd, Ni, Zn, Pb, Cu, and Cr, and the relationship between those trace elements and the soil properties in coastal wetlands using 28 profiles that were surveyed across the Diaokouhe Nature Reserve (DKHNR). The goal of this study is to investigate profile distribution characteristics of heavy metals in different wetland types and their variations with the soil depth to assess heavy metal pollution using pollution indices and to identify the pollution sources using multivariate analysis and sediment quality guidelines. Principal component analysis, cluster analysis, and pollution level indices were applied to evaluate the contamination conditions due to wetland degradation. The findings indicated that the concentration of trace elements decreased with the soil depth, while Cd increases with soil depth. The As concentrations in reed swamps and Suaeda heteroptera surface layers were slightly higher than those in other land use types. All six heavy metals, i.e., Ni, Cu, As, Zn, Cr, and Pb, were strongly associated with PC1 (positive loading) and could reflect the contribution of natural geological sources of metals into the coastal sediments. PC2 is highly associated with Cd and could represent anthropogenic sources of metal pollution. Most of the heavy metals exhibited significant positive correlations with total concentrations; however, no significant correlations were observed between them and the soil salt and soil organic carbon. Soil organic carbon exhibited a positive linear relationship with Cu, Pb, and Zn in the first soil layer (0–20 cm); As, Cr, Cu, Ni, Pb, and Zn in the second layer (20–40 cm); and As, Cr, Cu, Ni, Pb, and Zn in the third layer (40–60 cm). Soil organic carbon exhibited only a negative correlation with Cd (P?I _geo values), which averaged less than 0 in the three soil layers, this finding indicates that the soils have remained unpolluted by these heavy metals. The mean concentrations of these trace elements were lower than Class I criteria. The degradation wetland restoration suggestions have also been provided in such a way as to restore the reserved flow path of the Yellow River. The results that are associated with trace element contamination would be helpful in providing scientific directions to restore wetlands across the world.     

Using ecological memory as an indicator to monitor the ecological restoration of four forest plantations in subtropical China

A large area of plantations has been established worldwide and especially in China. Evaluating the restoration status of these plantations is essential for their long-term management. Based on our previous work, we used an ecological memory (EM) approach to evaluate four 26-year-old plantations that represent four common kinds of plantations in subtropical China, i.e., mixed broad-leaved plantation (MBP), mixed coniferous plantation (MCP), eucalyptus plantation (EP), and mixed legume plantation (MLP). Comparing them with the regional climax community, i.e., monsoon evergreen broad-leaved forest (BF), all four plantations accumulated nearly the same pattern of EM during succession. EM was >50 % for soil minerals, light conditions, soil age, soil animals, and soil microbes. EM was about 25 % for soil pollen and 10 % for birds, soil seed bank, and plant species. The total EM value of the four plantations ranged from 50.96 to 52.54, which indicated that all four plantations were in the regional, natural trajectory of succession and between the early and medium successional stages. The results indicated that natural succession processes are unlikely to be accelerated by planting late-stage tree species without sufficient EM. The results also demonstrated that all four plantations were in positive successional trajectories, and the positive succession dynamics were greater in the MLP and MCP. We suggest that the entire natural succession trajectory be used to evaluate the restoration of a site and that the ultimate restoration target be divided into several milestones along the reference trajectory to monitor progress. Forest restoration may be accelerated by starting with a minimum dynamic unit supporting sufficient EM.     

Determination of 16 polycyclic aromatic hydrocarbons in water using fluorinated polyaniline-based solid-phase microextraction coupled with gas chromatography

The study on the performance of a fluorinated polyaniline (PANI) as a fiber coating for solid-phase microextraction (SPME) had been reported and 16 polycyclic aromatic hydrocarbons (PAHs) were selected to evaluate the performance of this fiber. Various parameters including sample volume, extraction temperature, time of desorption and extraction, pH and ionic strength were investigated intensively. A direct comparison between PANI-SPME fiber and commercial fiber was conducted. The results showed that the PANI-SPME coating had high affinity towards target compounds and the proposed method was successfully applied for the detection of real samples: rainfall and Taihu Lake water collected from Southern China. The whole PANI-SPME-GC method offers acceptable accuracy, precision and sensitivity and low detection limits, which is applicable to monitor trace levels of PAHs in real water bodies.     

Characteristics and assessment of phthalate esters in urban dusts in Guangzhou city, China

Phthalate esters (PAEs) were examined in indoor and outdoor dust samples from the subtropical city of Guangzhou, China. The ∑(16)PAEs concentrations ranged from 121 to 3,223 μg g(-1) dust, with the median concentration of 840 μg g(-1) dust. Significantly higher concentrations of PAEs in dust samples were found in offices where electrical and electronic devices, carpet pads, and office furniture were widely used. Of the 16 PAEs, diisobutyl phthalate (DiBP), di-n-butyl phthalate (DnBP), and di(2-ethylhexyl) phthalate (DEHP) dominated the PAEs in indoor and outdoor dust samples, and accounted for >96.8% and >93.1% of the ∑(16)PAEs concentrations, respectively. The median daily inhalation exposure of ∑(16)PAEs were 3.53 and 0.247 μg kg(-1) body weight day(-1), and at the 95(th) percentile were 7.62 and 0.530 μg kg(-1) body weight day(-1), up on the measured concentrations and estimated dust ingestion rates, respectively, for toddles and adults. The ubiquitous distribution of PAEs as noted in this study suggests the need for detailed assessment of PAEs concentrations using more sites and to further investigate the factors influencing PAEs exposure in China.     

Sedimentary record of polycyclic aromatic hydrocarbons in a sediment core from a maar lake, Northeast China: evidence in historical atmospheric deposition

A maar lake is an excellent ecosystem to study the atmospheric deposition of pollutants, as its contaminants are primarily by atmospheric deposition. In this study, a sediment core from Sihailongwan Maar Lake, Northeast China, was collected and the historical atmospherically deposited polycyclic aromatic hydrocarbons (PAHs) were analyzed. The concentrations of TPAHs (the sum of the US EPA proposed 16 priority PAHs, excluding naphthalene and pyrene) ranged from 473.9 to 2289 ng g(-1) with a slow increasing stage in the deeper sediments and a sharp increasing stage in the upper sediments. The input rate of TPAHs, especially that of PAH(9) (the sum of fluoranthene, benzo(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene, indeno(1,2,3-cd)pyrene, dibenzo(ah)anthrathene, and benzo(ghi)perylene), correlated well to the Chinese historical socioeconomic data. This indicates that sediment PAHs were mainly derived from human activities and PAH(9) can be regarded as a better indicator of the local socioeconomic development. Source identification suggested that PAHs were originated primarily from mixed sources (e.g., coal and biomass burning and petroleum combustion), except for perylene which was mostly of diagenetic origin. In addition, the down-core PAHs profile clearly illustrated that PAHs sources in Northeast China experienced a transformation from low- and moderate temperature to high-temperature combustion processes, especially after the late 1980s. Additionally, an ecological risk assessment using two redefined biological thresholds (TEQ(ERL) and TEQ(ERM)) indicated that most of the PAHs measured in the present sediment core would not cause an immediate toxic effect; only FLU and PHEN are a potential source of concern for biological impairment.     

Water chemistry in 179 randomly selected Swedish headwater streams related to forest production,clear-felling and climate

From a policy perspective, it is important to understand forestry effects on surface waters from a landscape perspective. The EU Water Framework Directive demands remedial actions if not achieving good ecological status. In Sweden, 44 % of the surface water bodies have moderate ecological status or worse. Many of these drain catchments with a mosaic of managed forests. It is important for the forestry sector and water authorities to be able to identify where, in the forested landscape, special precautions are necessary. The aim of this study was to quantify the relations between forestry parameters and headwater stream concentrations of nutrients, organic matter and acid-base chemistry. The results are put into the context of regional climate, sulphur and nitrogen deposition, as well as marine influences. Water chemistry was measured in 179 randomly selected headwater streams from two regions in southwest and central Sweden, corresponding to 10 % of the Swedish land area. Forest status was determined from satellite images and Swedish National Forest Inventory data using the probabilistic classifier method, which was used to model stream water chemistry with Bayesian model averaging. The results indicate that concentrations of e.g. nitrogen, phosphorus and organic matter are related to factors associated with forest production but that it is not forestry per se that causes the excess losses. Instead, factors simultaneously affecting forest production and stream water chemistry, such as climate, extensive soil pools and nitrogen deposition, are the most likely candidates The relationships with clear-felled and wetland areas are likely to be direct effects.     

废弃矿山生态复绿常用17种植物叶绿素含量及SOD和POD活力测定

选用废弃矿山绿化常用的禾本科、豆科、葡萄科和紫葳科共17种为实验材料,测定了其叶绿素各组分含量及超氧岐化酶(SOD)和过氧化物酶(POD)活力,结果表明:叶绿素a、b类胡萝卜素和叶片色素总质量比最高的植物分别是胡枝子、狗牙根、牧草型狗牙根和狗牙根,其质量比分别为2.46 mg/g.FW、1.10 mg/g.FW、0.32 mg/g.FW和3.63 mg/g.FW;4者质量比最低的是紫穗槐、三出叶爬山虎、芒和紫穗槐,为1.10 mg/g.FW、0.48 mg/g.FW、0.08 mg/g.FW和1.70 mg/g.FW。ωa(叶绿素a)/ωb(叶绿素b)最高的是牧草型狗牙根,为3.03 mg/g.FW,最低的是芒,仅为1.65 mg/g.FW。POD和SOD活力最高的是网络崖豆藤和芒,达477.00 U和217.20 U,最低的是牧草型狗牙根和紫穗槐,仅为24 U和39.43 U。     

Determination of hydrazine hydrate based on electrochemiluminescence of Ru(bpy) 3 2+

Considering of the basic properties and also the two nitrogen atoms in the structure, hydrazine hydrate was employed to be an amine additive candidate, to build a Ru(bpy) ₃ ²⁺ /hydrazine electrochemiluminescence (ECL) system, and ECL of Ru(bpy) ₃ ²⁺ has been employed for the determination of hydrazine hydrate in the paper. The result demonstrated that the logarithmic ECL increasing (ΔECL?=?ECL_{after addition of hydrazine}???ECL_{before addition of hydrazine}) versus the logarithmic concentration of hydrazine hydrate is linear over a concentration range of 1.0?×?10^?9 to 1.0?×?10^?5?mol/L, on both glassy carbon and Pt electrodes in a pH 9 phosphate buffer. The hydrazine hydrate detection limit was down to 1.0?×?10^?9?mol/L, comparatively lower than other detection methods. To check its applicability, the proposed method was applied to the determination of hydrazine hydrate added into a tap water sample with good reproducibility and stability. All these provide a possibility to develop a novel ECL detection method for hydrazine in water.     

杭州夏季一次降雨过程雨水中全氟化合物及主要化学组分的变化特征

采用分段采样的方式收集杭州市2018年8月2日—3日一场降水样品,测定其中16种全氟化合物（PFCs）及主要化学组分浓度。结果发现,此次降雨过程水样的pH值范围为5.04～5.32,均为弱酸性降水,酸雨类型为复合型,检出的主要阳离子为NH+4,主要阴离子为SO2-4和NO-3;样品中检出7种中短链PFCs,包括2种全氟烷基磺酸（PFSAs）和5种全氟烷基羧酸（PFCAs）,ΣPFCs质量浓度范围为4.41 ng/L～25.2 ng/L,主要污染因子全氟辛酸（PFOA）质量浓度范围为096 ng/L～13.1 ng/L;降雨过程对大气污染清除作用的统计结果表明,区域大气环境中的主要化学组分及除全氟丁酸（PFBA）之外的PFCs污染主要吸附在云下大气颗粒物上;雨水中各污染因子浓度变化特征及相关性统计结果提示,杭州市大气中PFCAs和PFSAs两类PFCs可能来自不同的污染源。     

济南市环境空气VOCs污染特征及来源识别

对济南市2010年6月至2012年5月环境空气中56种挥发性有机污染物(VOCs)进行在线气相色谱监测,研究其污染特征并识别其主要来源。结果表明,该期间总挥发性有机化合物(TVOCs)变化规律基本一致,其平均浓度水平夏季冬季秋季春季;TVOCs浓度的日变化趋势呈双峰分布,与早晚交通高峰相吻合;济南市城区环境空气中VOCs的主要物种是C3~C5的烷烃、丙烯、顺-2-丁烯、甲苯和间、对二甲苯等;不同季节环境空气中VOCs的主要物种基本一致,夏季烯烃所占比重高于其他季节;烷烃、烯烃与TVOCs的浓度日变化趋势相似,呈明显的双峰状,而芳香烃浓度日变化规律双峰特征不明显。济南市城区VOCs的主要来源为汽车尾气、工业源、燃烧源。