Impacts of mussel dredging on sediment phosphorus dynamics in a eutrophic Danish fjord

Effects of mussel dredging on sediment metabolism (oxygen uptake and sulfate reduction rates) and phosphorus dynamics (flux across sediment-water interface and sequential extraction) were examined in Limfjorden (Denmark) during spring (May) and summer (August). Sediment samples were taken during mussel dredging and in addition an experimental simulation of the dredging was performed to investigate short-term changes in phosphorus (P) dynamics. Iron-bound P was reduced by up to 2/3 in the surface layer in the dredging track (from 31 to 8?mmol?P?m^?2), whereas the dissolved P-pools and less reactive particulate pools were not affected by dredging. Sediment oxygen consumption was enhanced immediately after dredging, but returned to the initial level after 4 days (20–40?mmol?m^?2?d^?1). The enhanced consumption was attributed to reoxidation of reduced compounds released during dredging. Sulfate reduction rates were high in the area (13–15?mmol?m^?2?d^?1) and sulfides competed with P for oxidized iron resulting in low iron-bound pools in the area (<4% of total P pools). Sulfate reduction rates were stimulated by the resuspension of sediments, especially in August, where a subsurface maximum was found, possibly due to a mixing of labile organic matter into these layers. In contrast sulfate reduction rates were reduced in the dredging track due to removal of labile organic matter from the surface layers. The loss of P during dredging was to some extent counteracted by regeneration of iron-bound P pools in the surface layers. The release of P due to mussel dredging was estimated to be in the same order of magnitude as the annual loading from the catchments and point sources to Limfjorden.     

Litter decomposition and nitrogen mineralization from an annual to a monthly model

The forest litter decomposition model (FLDM) described in this paper provides an important basis for assessing the impacts of forest management on seasonal stream water quality and export of dissolved organic carbon (DOC). By definition, models with annual time steps are unable to capture seasonal, within-year variation. In order to simulate seasonal variation in litter decomposition and DOC production and export, we have modified an existing annual FLDM to account for monthly dynamics of decomposition and residual mass in experimental litterbags placed in 21 different forests across Canada.The original annual FLDM was formulated with three main litter pools (fast, slow, and very slow decomposing litter) to address the fact that forest litter is naturally composed of a mixture of organic compounds that decompose at different rates. The annual FLDM was shown to provide better simulations than more complex models like CENTURY and SOMM.The revised monthly model retains the original structure of the annual FLDM, but separates litter decomposition from nitrogen (N) mineralization. In the model, monthly soil temperature, soil moisture, and mean January soil temperature are shown to be the most important controlling variables of within-year variation in decomposition. Use of the three variables in a process-based definition of litter decomposition is a significant departure from the empirical definition in the annual model. The revised model is shown to give similar calculations of residual mass and N concentration as the annual model (r² = 0.91, 0.78), despite producing very different timeseries of decomposition over six years. It is shown from a modelling perspective that (i) forest litter decomposition is independent of N mineralization, whereas N mineralization is dependent on litter decomposition, and (ii) mean January soil temperature defines litter decomposition in the summer because of winter-temperatures’ role in modifying forest-floor microorganism community composition and functioning in the following summer.     

浅谈顶吹氧气转炉炼钢湿法除尘的脱硫功能

立足鞍钢生产实际,肯定了氧气转炉炼钢湿法除尘的降温功能与作用、除尘功能与作用,揭示了氧气转炉炼钢湿法除尘装置在碱性洗涤溶液(pH=12.0～13.5)作用下的潜在脱硫功能与作用(脱硫率99.56%),为“分体组合”选型湿法“降温除尘脱硫”设备处理高温含硫气体提供了科学依据。     

Removal of dissolved organic matter in municipal effluent with ozonation, slow sand filtration and nanofiltration as high quality pre-treatment option for artificial groundwater recharge

In the paper the combination process of ozonation, slow sand filtration (SSF) and nanofiltration (NF) was investigated with respect to dissolved organic matter (DOM) removal as high quality pre-treatment option for artificial groundwater recharge. With the help of ozonation leading to breakdown of the large organic molecules, SSF preferentially removes soluble microbial by-product-like substances and DOM with molecular weight (MW) less than 1.0 kDa. NF, however, removes aromatic, humic acid-like and fulvic acid-like substances efficiently and specially removes DOM with MW above 1.0 kDa. The residual DOM of the membrane permeate is dominated by small organics with MW 500 Da, which can be further reduced by the aquifer treatment, despite of the very low concentration. Consequently, the O₃/SSF/NF system offers a complementary process in DOM removal. Dissolved organic carbon (DOC) and trihalomethane formation potential (THMFP) can be reduced from 6.5 ± 1.1 to 0.7 ± 0.3 mg L⁻¹ and from 267 ± 24 to 52 ± 6 μg L⁻¹, respectively. The very low DOC concentration of 0.6 ± 0.2 mg L⁻¹ and THMFP of 44 ± 4 μg L⁻¹ can be reached after the aquifer treatment.     

基于WASP 7模型的水质模拟应用——以淮沭新河东海段为例

应用WASP 7模型的EUTRO子模块对淮沭新河东海段的溶解氧(DO)和化学需氧量(COD)指标进行模拟研究,采用2014年与2015年的水文、水质数据进行模型参数率定,并以2016年1月—2017年9月的水质数据进行验证,验证结果为DO和COD的模拟值与实际值的相对误差分别能控制在15%和10%以内,线性回归分析结论显示相关系数R2均在0.9以上,表明两者的吻合度较高。     

Simulating Dissolved Organic Carbon Dynamics at the Swedish Integrated Monitoring Sites with the Integrated Catchments Model for Carbon,INCA-C

Surface water concentrations of dissolved organic carbon ([DOC]) are changing throughout the northern hemisphere due to changes in climate, land use and acid deposition. However, the relative importance of these drivers is unclear. Here, we use the Integrated Catchments model for Carbon (INCA-C) to simulate long-term (1996–2008) streamwater [DOC] at the four Swedish integrated monitoring (IM) sites. These are unmanaged headwater catchments with old-growth forests and no major changes in land use. Daily, seasonal and long-term variations in streamwater [DOC] driven by runoff, seasonal temperature and atmospheric sulfate (SO₄ ²⁻) deposition were observed at all sites. Using INCA-C, it was possible to reproduce observed patterns of variability in streamwater [DOC] at the four IM sites. Runoff was found to be the main short-term control on [DOC]. Seasonal patterns in [DOC] were controlled primarily by soil temperature. Measured SO₄ ²⁻ deposition explained some of the long-term [DOC] variability at all sites.     

Methylmercury speciation in the dissolved phase of a stratified lake using the diffusive gradient in thin film technique

The diffusive gradient in thin film (DGT) technique was successfully used to monitor methylmercury (MeHg) speciation in the dissolved phase of a stratified boreal lake, Lake 658 of the Experimental Lakes Area (ELA) in Ontario, Canada. Water samples were conventionally analysed for MeHg, sulfides, and dissolved organic matter (DOM). MeHg accumulated by DGT devices was compared to MeHg concentration measured conventionally in water samples to establish MeHg speciation. In the epilimnion, MeHg was almost entirely bound to DOM. In the top of the hypolimnion an additional labile fraction was identified, and at the bottom of the lake a significant fraction of MeHg was potentially associated to colloidal material. As part of the METAALICUS project, isotope enriched inorganic mercury was applied to Lake 658 and its watershed for several years to establish the relationship between atmospheric Hg deposition and Hg in fish. Little or no difference in MeHg speciation in the dissolved phase was detected between ambient and spike MeHg.     

钙钛矿型SrFeO_(3-λ)催化降解水溶性染料

采用柠檬酸络合法合成了钙钛矿型 Sr Fe O3-λ复合氧化物 ,以其为催化剂对不同水溶性染料溶液进行降解脱色试验 ,各种染料的脱色率均较高 ,表明 Sr Fe O3-λ具有很好的催化活性 ,这主要与 Sr Fe O3-λ中 Fe离子的变价和存在大量氧空位有关。     

Quantifying uranium complexation by groundwater dissolved organic carbon using asymmetrical flow field-flow fractionation

The long-term mobility of actinides in groundwaters is important for siting nuclear waste facilities and managing waste-rock piles at uranium mines. Dissolved organic carbon (DOC) may influence the mobility of uranium, but few field-based studies have been undertaken to examine this in typical groundwaters. In addition, few techniques are available to isolate DOC and directly quantify the metals complexed to it. Determination of U-organic matter association constants from analysis of field-collected samples compliments laboratory measurements, and these constants are needed for accurate transport calculations. The partitioning of U to DOC in a clay-rich aquitard was investigated in 10 groundwater samples collected between 2 and 30 m depths at one test site. A positive correlation was observed between the DOC (4-132 mg/L) and U concentrations (20-603 microg/L). The association of U and DOC was examined directly using on-line coupling of Asymmetrical Flow Field-Flow Fractionation (AsFlFFF) with UV absorbance (UVA) and inductively coupled plasma-mass spectrometer (ICP-MS) detectors. This method has the advantages of utilizing very small sample volumes (20-50 microL) as well as giving molecular weight information on U-organic matter complexes. AsFlFFF-UVA results showed that 47-98% of the DOC (4-136 mg C/L) was recovered in the AsFlFFF analysis, of which 25-64% occurred in the resolvable peak. This peak corresponded to a weight-average molecular weight of about 900-1400 Daltons (Da). In all cases, AsFlFFF-ICP-MS suggested that相似文献   

Ecological study of river Suswa: modeling DO and BOD

In this paper limnological status of river Suswa was observed for a period of two years. A water quality Beck modified Khanna Bhutiani model (BMKB model) was developed to calculate DO (dissolved Oxygen) and BOD (biochemical oxygen demand). The model was developed to calculate DO and BOD by using DO/BOD of same place and upstream in previous season which results in Single output. This model gives the seasonal value on the basis of previously taken upstream and downstream observations/concentrations of DO and BOD. The model was calibrated and verified for the water quality data (Physico-chemical data) of samples collected from river Suswa in different seasons. The model gave good agreement between data observed by it and the data observed manually, thus substantiating the validity of the model. Only minor differences were observed in physical, chemical and heavy metals of all the four sampling stations during the course of study.