东海表层水体中的多环芳烃及其沉积通量估算

以东海陆架水体中溶解态多环芳烃(PAHs)含量为基础,引入颗粒相-水相间的物质吸附系数(Koc)计算悬浮颗粒物中PAHs有机碳归一化含量,结合陆架沉积物有机碳的年埋藏通量,估算东海陆架沉积物中PAHs沉积通量。结果显示:水体中溶解态的15种PAHs总含量为(701±392)ng/L,变化范围为412~1 032ng/L,PAHs组成以3环为主。计算得到的悬浮颗粒物中15种PAHs有机碳归一化含量为20~28μg/g,对应的PAHs沉积通量为150~210t/a。估算结果与实测沉积物中PAHs含量和沉积通量结果基本吻合,表明实验室模拟实验获取的化合物Koc值适用于东海颗粒相-水相间的分配模型,证实悬浮颗粒物有机碳含量在控制PAHs两相分布过程中起着重要作用。同时,该方法为海洋沉积物中PAHs沉积通量的估算提供一种新途径。     

白令海颗粒有机物碳、氮同位素组成及其生物地球化学意义

Stable carbon and nitrogen isotopic composition of particulate organic matter(POM) were measured for samples collected from the Bering Sea in 2010 summer. Particulate organic carbon(POC) and particulate nitrogen(PN) showed high concentrations in the shelf and slope regions and decreased with depth in the slope and basin, indicating that biological processes play an important role on POM distribution. The low C/N ratio and heavy isotopic composition of POM, compared to those from the Alaska River, suggested a predominant contribution of marine biogenic organic matter in the Bering Sea. The fact that δ13C and δ15N generally increased with depth in the Bering Sea basin demonstrated that organic components with light carbon or nitrogen were decomposed preferentially during their transport to deep water. However, the high δ13C and δ15N observed in shelf bottom water were mostly resulted from sediment resuspension.     

Prediction of depth‐integrated fluxes of suspended sediment in the Amazon River: particle aggregation as a complicating factor

Large rivers have been previously shown to be vertically heterogeneous in terms of suspended particulate matter (SPM) concentration, as a result of sorting of suspended solids. Therefore, the spatial distribution of suspended sediments within the river section has to be known to assess the riverine sedimentary flux. Numerous studies have focused on the vertical distribution of SPM in a river channel from a theoretical or experimental perspective, but only a few were conducted so far on very large rivers. Moreover, a technique for the prediction of depth‐integrated suspended sediment fluxes in very large rivers based on sediment transport dynamics has not yet been proposed. We sampled river water along depth following several vertical profiles, at four locations on the Amazon River and its main tributaries and at two distinct water stages. Depending on the vertical profile, a one‐ to fivefold increase in SPM concentration is observed from river channel surface to bottom, which has a significant impact on the ‘depth‐averaged’ SPM concentration. For each cross section, a so‐called Rouse profile quantitatively accounts for the trend of SPM concentration increase with depth, and a representative Rouse number can be measured for each cross section. However, the prediction of this Rouse number would require the knowledge of the settling velocity of particles, which is dependent on the state of aggregation affecting particles within the river. We demonstrate that in the Amazon River, particle aggregation significantly influences the Rouse number and renders its determination impossible from grain‐size distribution data obtained in the lab. However, in each cross section, the Rouse profile obtained from the fit of the data can serve as a basis to model, at first order, the SPM concentration at any position in the river cross section. This approach, combined with acoustic Doppler current profiler (ADCP) water velocity transects, allows us to accurately estimate the depth‐integrated instantaneous sediment flux. Copyright © 2010 John Wiley & Sons, Ltd.     

Sediment and particulate phosphorus characteristics in grassed waterways from row crop corn and alfalfa fields collected by manual University of Exeter samplers and automatic sampling

Phosphorus (P) export from agricultural lands above known threshold levels can result in adverse impacts to receiving water quality. Phosphorus loss occurs in dissolved and sediment‐bound, or particulate phosphorous (PP), forms, with the latter often dominating losses from row‐cropped systems. To target practices, land managers need good computer models and model developers need good monitoring data. Sediment monitoring data (e.g. radiometric finger printing and sediment P sorption capacity) can help identify sediment source areas and improve models, but require more sediment mass than is typically obtained by automatic sampling. This study compares a simple suspended sediment sampler developed at the University of Exeter (UE) with automatic sampling in intermittent channels draining corn and alfalfa fields. The corn field had a greater runoff coefficient (27%) than alfalfa (11%). No differences were found in enrichment ratios (sediment constituent/soil constituent) in PP (PP_ER) or percent loss on ignition (LOI_ER) between paired UE samplers on corn. The median LOI_ER for the UE samplers (1·9%) did not differ significantly (p > 0·13) from the automatic sampler (2·0%). The PP_ER from the UE samplers was on average 20% lower than the automatic samplers. A correlation (r² = 0·75) was found between sediment PP and % LOI from automatic samplers and UE samplers for particles < 50 µm, while for > 50 µm PP concentration did not change with changes in % LOI. Sediment ammonium‐oxalate extractable metals were similarly related to LOI, with the strongest correlation for iron (r² = 0·71) and magnesium (r² = 0·70). Copyright © 2011 John Wiley & Sons, Ltd.     

DISSOLVED AND PARTICULATE ORGANIC CARBON IN YANTAI SISHILI BAY AQUICULTURE WATERS

Investigation of dissolved organic carbon (DOC) and particulate organic carbon (POC) at 12 stations in Yantal Sishili Bay in May, August, and November of 1997 and March and May of 1998 showed that DOC concentrations varied from 1.14 mg/L to 5.35 mg/L; that the average values at all staticrLs ineach entise varied from 1.52 mg/L to 2.12 mg/L; that POC concentrafions varied from 0.049 mg/L to 1.411mg/L; and averaged 0.159 mg/L to 0.631 mg/L in each cruise. Horizontal distribution of DOC was influ-enced by factors such as continental input, organism activity, temperature, aquieulture environment, etc. The higher POC concentration occurred along the coast. The vertical distribution of DOC and POC changed obviously in spring and summer, but not obviously in autumn and winter. DOC concentration was highest in summer and POC in spring; both were lowest in winter. The seasonal change of DOC was con-sistent with primary productivity seasonal variation, and that of POC was consistent with ehlorophyll-a sea-sanal variation. The seasonal change trend of the C/N ratio of dissolved organic matter was obvious, but the C/N ratio of particulate organic matter had no such trend.     

MOLAR RATIOS OF C, N, P OF PARTICULATE MATTER AND THEIR VERTICAL FLUXES IN THE YELLOW SEA

The vertical fluxes and molar ratios of carbon, nitrogen and phosphorus of suspended particulate matter in the Yellow Sea were studied based on the analysis of suspended particulate matter,sediments and sinking particles obtained by use of moored sediment traps. The POC ： PON ratios indicate that most of the particulate organic matter in the Yellow Sea water column comes from marine life rather than the continent. The vertical fluxes of SPM, POC, PON and POP in the Yellow Sea are much higher than those in other seas over the world, and present a typical pattern in shallow epicontinental seas. The estimated residence time of the bioactive elements showed that the speed of the biogeochemical process of materials in the Yellow Sea is much shorter than that in the open ocean as there was high primary productivity in this region.     

Arsenic Speciation in Lichens and in Coarse and Fine Airborne Particulate Matter by HPLC–UV–HG–AFS

A three-step sequential extraction procedure with Milli-Q, CaCl₂ and H₃PO₄ was applied for extraction of arsenic species in lichen transplants and airborne particulate matter (fine and coarse fractions). The samples used in this work were collected in 1994–1995 near coal-fired power plants. Both transplant lichens and airborne particulate matter were submitted to the same environment simultaneously. Arsenic species identification and quantification was performed by HPLC–UV–HG–AFS. Inorganic forms of arsenic (arsenite and arsenate) were present in significant amounts in most of the samples. Only in lichens also organic forms of arsenic (monomethyl arsonic acid and dimethyl arsinic acid) were identified which may indicate biotransformation of inorganic arsenic.     

Analysis of mass concentration of atmospheric particulate matter in a sandstorm course and its affecting factors in the Taklimakan Desert

During the course of a major sandstorm from April 17 to April 23, 2008 in the Taklimakan Desert, data pertaining to the mass concentrations of different-sized atmospheric particulate matter were observed continuously with Grimm 1.108, Thermo RP 1400a, TSP, and CAWS-600 instruments. The results showed that: (1) during the entire sandstorm process there were some differences between the daily mean particle concentration peaks and the hourly mean particle concentration peaks because the actual sandstorm lasted for only about 4 hr, whereas more particles were accumulated in the floating dust days before and after the actual sandstorm; (2) the intensity of the sandstorm was enhanced with the increase of wind speed, and this was related to the peak mass concentrations of atmospheric particulate matter; the wind speed directly affected the concentration of atmospheric particulate matter: the higher the wind speed, the higher the mass concentration (>0.23 μm was 39,496.5 μg/m³, and >20.0 μm was 5,390.7 μg/m³); (3) the concentration changes of PM₁₀ and TSP were also related to the course and intensity of the sandstorm; and (4) the mass concentration of atmospheric particulate matter had the following sequence during the dust weather: clear day < floating dust < floating and blowing dust < sandstorm. Temperature, relative humidity, and barometric pressure are important factors affecting the strength of storms, which could also indirectly affect the concentration change of atmospheric particulate matter.     

北京市采暖期可吸入颗粒物时空分布特征及源追踪

可吸入颗粒物是北京市大气主要污染物之一,春秋两季的沙尘天气除部分是由于受到区域气流的影响外,多数情况下是原地污染造成,尤其是冬季采暖期。本文通过遥感技术和地面监测结合的方法,研究采暖期北京市近地面不同粒径可吸入颗粒物时空分布规律及其与影响因素间的相互关系。应用高分辨率遥感影像分析下垫面的变化,应用地面观测仪器收集不同粒径颗粒物的含量,并分析颗粒物的化学组成;应用地理信息系统的空间分析技术,研究颗粒物的分布与下垫面的关系。研究表明,可吸入颗粒物污染分布和下垫面介质、人为污染源、人口密度、气象因素有非常密切的关系。     

Evidence for microbiological manganese oxidation in the river Tamar Estuary, South West England

Water samples from the Tamar Estuary oxidized manganese when supplemented with Mn²⁺ (2 mgl⁻¹). The rates of oxidation were depressed in the presence of various metabolic inhibitors. The effect of Mn²⁺ and temperature on the rate of manganese oxidation suggested that a biological process was largely responsible for converting Mn²⁺ to Mn⁴⁺. Rates of manganese oxidation were much higher in freshwater (3·32 μgl⁻¹ h⁻¹ in water containing 30 mgl⁻¹ of suspended matter) than in saline water (0·7 μgl⁻¹ h⁻¹ in water of salinity 32‰) containing the same amount of particulate matter. The rate of manganese oxidation was proportional to the particulate load (up to 100 mgl⁻¹ particulates).