Distribution, behavior, and risk assessment of chlorinated paraffins in paddy plants throughout whole growth cycle.

Paddy plants provide staple food for 3 billion people worldwide. This study explores the environmental fate and behavior of a high-volume production emerging contaminants chlorinated paraffins (CPs) in the paddy ecosystem. Very-short-, short-, medium-, and long-chain CPs (vSCCPs, SCCPs, MCCPs, and LCCPs, respectively) were analyzed in specific tissue of paddy plants at four main growth stages and soils from the Yangtze River Delta, China throughout a full rice growing season. The total CP concentrations in the paddy roots, stalks, leaves, panicles, hulls, rice, and soils ranged from 181 to 1.74 × 103, 21.7-383, 19.6-585, 108-332, 245-470, 59.6-130, and 99.6-400 ng/g dry weight, respectively. The distribution profile indicated the translocation of SCCPs and MCCPs from soils to paddy tissue, highlighting their elevated bioaccumulative potential. The evolution of CP level/mass/pattern during the whole growth cycle suggested atmospheric CPs deposition on leaves and hulls, as well as stalk-rice transfer. CSOIL plant uptake model well predicted the level, distribution pattern, and bioconcentration factors (BCFs) of SCCPs and MCCPs in paddy shoot and recognized the soil-air-shoot pathway as the major contributor. Moreover, risk evaluation indicated that MCCPs intake and subsequent risks dominated the total exposure to CPs via rice ingestion. This is the first report on the occurrence, fate and risk assessment of all CPs classes in paddy ecosystems, and the results underline the potential health effects caused by the in-use MCCPs via rice ingestion.

Polycyclic aromatic hydrocarbons in sedimentary cores of Tibetan Plateau: Influence of global warming on cold trapping.

Cold condensation is an important pathway for polycyclic aromatic hydrocarbons (PAHs) depositing at remote alpine lakes after long-range atmospheric transportation. However, in the context of global warming, the obvious temperature rise in the Tibetan Plateau (TP) might have an impact on the air deposition of PAHs by controlling the extent of cold condensation. To investigate the influence of rising temperatures on the atmospheric deposition of PAHs, two dated sedimentary cores from Pumoyum Co Lake (PC) and Selin Co Lake (SC) were collected, respectively and concentrations of 16 individual PAHs were measured. In both PC and SC, the total concentration of 16 PAHs presented relatively lower levels in four historical periods of "hot anomaly" including 1973-1975, 1988-1989, 1998-1999, and 2006-2007. This indicated that the hot temperatures might restrict the atmospheric deposition of PAHs. Besides, the results of the principal component analysis did discriminate those "hot anomalies". As the temperature kept increasing in TP, for low molecular weight PAHs and high molecular weight PAHs, the influence of rising temperatures on the cold condensation was different. Therefore, it was identified that the effect of global warming on the environmental fate of POPs cannot be neglected, especially in alpine regions like TP.

Determination of Cadmium in Water Samples by Electrochemical Hydride Generation Atomic Fluorescence Spectrometry Using Series Graphite Tubes as Electrolytic Cells under Constant Voltage.

An electrochemical vapor generation (EcHG) system to determine the cadmium content using atomic fluorescence spectrometry has been established. The EcHG system uses two serially-connected graphite tubes as two electrolysis cells and an AC to DC power wall plug adapter with the constant voltage mode as a power supply. The system did not have an ion exchange membrane and only needed a pump to transport the feed solution and waste. Under these optimized conditions, the detection limit (3σ) and the relative standard deviation were 0.05 ng mL-1 and 3.2%, respectively. The EcHG efficiency was 38.4 ± 2.2%. The proposed technique has been successfully applied to determine the cadmium in three certified reference materials for environmental water and two drinking water samples.

The sedimentary record of polycyclic aromatic hydrocarbons in Yamzho Yumco Lake: evolution of local sources and adsorption dynamic in the Tibetan Plateau.

With the rapid increase in anthropogenic activities, the local emissions of polycyclic aromatic hydrocarbons (PAHs) in background regions, such as the Tibetan Plateau (TP), have attracted great attention. The deposition of PAHs in lake sediments provides a historical evolutionary record of such compounds in these regions. To investigate the evolution of PAHs in the TP, two sedimentary cores from Yamzho Yumco Lake were collected and dated at high resolution, and the concentrations of 16 PAHs and sediment properties were also analyzed. The total concentrations of the 16 PAHs ranged from 6.52 to 57.97 ng/g (dry weight) in YC1 and from 0.91 to 4.57 ng/g (dry weight) in YC2. According to the methods of principal component analysis (PCA) followed by multilinear regression analysis (MLRA), four sources of PAHs in the sediments were qualitatively and quantitatively identified, such as petroleum combustion, petrogenic, coal combustion, and biomass burning. Thus, the historical evolution of PAHs was summarized. In addition, the transported distance from local PAH emission sources was found to greatly affect the composition and concentration of PAHs in sites YC1 and YC2. Specifically, local sources contributed a greater proportion of heavy molecular weight (HMW) PAHs in YC1 and a higher proportion of light-molecular-weight (LMW) PAHs in YC2. Moreover, fine particles (size < 20 µm) were found to play a significant role in adsorbing PAHs in sediments. Furthermore, ∑16PAHs in sediments were linearly correlated with the percentage of fine particles (size < 20 µm). This study provides a first example to investigate the historical evolution of PAH local emission in background regions by using lake sedimentary records, especially in the TP. Specifically, different local sources were identified using the methods of PCA followed by MLRA, and PAHs in TP sediments were predominantly adsorbed by fine particles rather than by total organic carbon (TOC) because the amount of TOC was limited.

Room-temperature Chelate Vapor Generation of Lead Using Ammonium O,O-Diethyl Dithiophosphate as a Chelating Reagent and Determination by Atomic Fluorescence Spectrometry in Environmental Water Samples.

A novel gas-liquid separator (GLS) system for chelate vapor generation (Che-VG) combined with AFS was developed for the determination of trace Pb. It was shown that Pb can form a volatile chelate by mixing of Pb with ammonium O,O-diethyldithiophosphate (DEDTP) in various aqueous solutions. Under the optimal conditions (frit pores of the GLS, 5 - 15 µm; solution pH, 6.7; DEDTP concentration, 0.4%; flow rate of the two feed solutions in the on-line mode, 1.2 mL min-1; and carrier gas flow rate, 150 mL min-1), the calibration curve was linear up to 100 ng mL-1 Pb. The limit of detection (LOD) was 1.1 ng mL-1. The relative standard deviation was 5.6% for eleven replicate determinations of 10 ng mL-1 Pb. The efficiency of Che-VG was estimated to be 12%, and the volatile Pb species was preliminarily studied by ICP-OES. This method was applied to determine trace Pb in water samples.

Insight into the local source of polybrominated diphenyl ethers in the developing Tibetan Plateau: The composition and transport around the Lhasa landfill.

In the background region of the Tibetan Plateau (TP), the rapid urbanization probably results in the massive generation of persistent organic pollutants (POPs), which lacks monitoring and evaluation. Since landfill could serve as an important sink of the locally used POPs, the analysis of POPs in the Tibetan landfill area might help us to understand the source composition and their transport in the TP. In this study, the concentration variations of polybrominated diphenyl ethers (PBDEs) in five soil profiles and seven surficial sediments around the largest Tibetan landfill were investigated. The total concentrations of PBDEs ranged from 128 to 1219 ng/kg in soils, and from 447 to 7295 ng/kg in sediments. The dominance of nona- and deca-BDEs possibly indicated the wide usage of deca-BDE as flame retardant in the TP. The vertical and spatial distribution patterns of PBDEs within soils plausibly revealed their main transport pathways by atmospheric dispersion and leachate seepage from landfill. Based on principal components analysis and multiple linear regression, these two pathways were estimated to account for 61% and 39% of the total concentrations, respectively. Additionally, the spatial and vertical distributions of octa-to deca-BDEs within soils were significantly influenced by soil particle size. Although the PBDEs inventory in the study area was comparatively low, the rapid urbanization in the TP might dramatically accelerate the PBDE emissions in the future. This study firstly introduced the presence of local PBDEs in the TP, and the inventory already influenced the surrounding environment. Once involved in the regional cycle of the TP, the local source of PBDEs from waste might significantly serve to raise background level resulting otherwise primarily from long-range atmospheric transport.

Organochlorine pesticides in the sedimentary core of the southern Tibetan Plateau: The missing pieces induced by lateral remobilization.

The sedimentary core in remote alpine lakes has been recognized as an ideal proxy to reconstruct the emission and air deposition histories of persistent organic pollutants (POPs). Nevertheless, POPs formerly stored in a catchment might also contribute to the variation in the lake sediment by lateral remobilization. In this study, to reveal the relative importance of lateral remobilization, we measured the vertical profiles and isomeric ratios of dichlorodiphenyltrichloroethanes (DDTs), hexachlorocyclohexanes (HCHs) and endosulfan in a dated sedimentary core collected from Lake Yamzho Yumco in the southern Tibetan Plateau. In addition to the flux peaks in the 1970s corresponding to the heavy atmospheric deposition of DDTs and HCHs, these pollutants' fluxes displayed rebounds in the flood periods, with characteristic low ratios of DDT/DDE (α-/ß-HCH). This might indicate a massive remobilization of "weathered" pesticides from catchment soil to the lake because of strong hydro-dynamics. Moreover, the relative contribution of lateral remobilization to the lake sediment in the past decades was recognized through the correlation between DDT/DDE (α-/ß-HCH) ratios and ∑DDT (∑HCH) fluxes. The results showed that the lateral remobilization contributed to 20-42% of the total fluxes. This study discriminated the air deposition from the contribution of lateral remobilization, which improves current understanding of the vertical POPs profiles in the sedimentary core.

Determination of Ammonium in Aqueous Samples by Gas Phase Light Scattering Using Hydrogen Chloride Gas as a Derivatizing Reagent Followed by Nondispersive Atomic Fluorescence Spectrometry.

A sensitive method was developed for the determination of ammonium in an aqueous solution based on gas phase light scattering. In a stream of carrier gas, the gaseous ammonia from the alkalized solution formed a volatile ammonium chloride derivative by reacting with gaseous hydrogen chloride; the gaseous ammonium chloride was analyzed by nondispersive atomic fluorescence spectrometry. The mechanisms of the method are elucidated based on evaporative light scattering detection. Parameters such as temperature, amount of sodium hydroxide, and carrier gas flow rate were studied. Under optimal conditions, the detection limit of ammonium-nitrogen was 0.045 µg. The method was successfully applied to the determination of ammonium in certified reference materials, and tap and seawater samples.

Cadmium accumulation and its effects on metal uptake in maize (Zea mays L.).

The effects of different concentrations of Cd on growth of maize (Zea mays L.) and metal uptake were investigated. Cd accumulations in roots and shoots and the interactions among other metals (Mn, Fe, Cu and Zn) were analyzed using inductively coupled plasma atomic emission spectrometry (ICP-AES). The concentrations of cadmium chloride (CdCl(2).2.5H2O) used ranged from 10(-4) M to 10(-6) M. Cd had stimulatory effects during the first 5 days on root length of Nongda No. 108 at 10(-6) M and 10(-5) M Cd concentrations. Seedlings exposed to 10(-4) M Cd solution exhibited substantial growth reduction, and root growth even stopped. Root growth of Liyu No. 6 was stimulated at concentrations of 10(-5) M and 10(-6) M Cd during the entire experiment (15 days). Cadmium inhibited root growth of Liyu No. 6 at 10(-4) M Cd after 10 days of treatment. The Cd accumulation in roots and shoots of the two cultivars increased significantly (P < 0.05) with increasing Cd concentration and duration of treatment. Cadmium concentrated mainly in the roots, and small amounts were transferred to shoots. The proportion of Cd in the roots of Nongda No. 108 decreased with increases in Cd concentrations and duration of treatment, except for the group exposed to 10(-4) M Cd. In Liyu No. 6, the proportion of Cd in the root decreased progressively with an increase in Cd concentrations. Liyu No. 6 has a greater ability to remove Cd from solution and accumulate it when compared with Nongda No. 108. Liyu No. 6 can be considered a Cd-hyperaccumulator, according to the current accepted shoot concentration that defines hyperaccumulation as 0.01% (w/w) for cadmium. This cultivar, producing many roots and a high biomass and with great ability to accumulate Cd can play an important role in the treatment of soils stressed by Cd.

[Determination of copper and chromium in the cartridges of permanent marker pen and ink by ICP-AES].

The method for the determination of copper and chromium in the cartridges of permanent pen oil base and ink by ICP-AES was reported. This mainly concerned the different methods for pretreatment of samples. The study indicated that the better method for the pretreatment of the cartridges of permanent pen and the ink containing resin is dry ashing at 550 degrees C followed by wet-decomposition with mixed acid (V(HNO3) : V(HClO4 = 3 : 1); the better method for the pretreatment of water soluble ink is hydrodigestion with mixed acid (V(HNO3 : V(HClO4 = 3 : 1). After suitable dilution with acid, copper and chromium were determinated by ICP-AES. It was shown that the method is reliable for the test of precision and accuracy. RSD and recovery were in the range of 5.9% - 7.9% and 90% - 104%, respectively.