广西北仑河口红树林保护区表层海水溶解态重金属时空分布及其影响因素

根据2013年5月(春季)和8月(夏季)对广西北仑河口红树林保护区的现场调查监测数据,研究了表层海水中溶解态重金属Cu、Zn、Pb、Cd、Cr、As、Hg的时空分布特征,探讨了其影响因素,并对其污染水平进行了评价。结果表明,表层海水各溶解态重金属的浓度、空间波动程度在春、夏季均存在一定的差异;Hg的污染明显超过国家一类海水水质标准,且夏季污染水平高于春季。Cu-Zn、Cu-Cd、Zn-Pb、Zn-Cd之间存在显著正相关,春、夏季As以及夏季Cr分别与盐度之间呈显著正相关,其他重金属与盐度之间无显著相关性。各重金属的时空分布主要受到陆源输入、沿岸江河冲淡水和海水盐度变化等因素的影响。     

Isotopic Composition of Dissolved Carbonates Meromictic Soda Lake Doroninskoe(Eastern Transbaikalia,Russia)

正1 Introduction Meromictic soda Lake Doroninskoe localized in the intermountain area,filled with continental sediments of the Mesozoic,in the upper basin of the river Amur.Coordinates of its location are N51°14'42"E112°14'40",     

环青海湖地下水溶解性碳的时空变化特征

区域地下水溶解性碳的时空变化特征研究对于认识区域物质循环和能量传递及推动区域生态可持续发展具有重要意义。本研究在青海湖流域冻结期和融化期分别收集了地下水、河水和湖水样品,研究了环青海湖地下水在冻结期和融化期的溶解性碳特征,并探究了不同类型地下水的溶解性碳特征及其对不同冻融时期的响应,最后揭示了环湖区域不同水体的溶解性碳的差异特征及影响因素。结果表明：冻结期地下水、河水和湖水的溶解性无机碳（DIC）均相对高于融化期,溶解性有机碳（DOC）均相对低于融化期。地下水、河水和湖水的溶解性碳均主要以DIC为主,DIC在溶解性碳的占比高达92%。地下水的DIC平均含量在基岩裂隙水、水量中等和浅埋藏的水文地质条件下相对较高,DOC平均含量在基岩裂隙水、水量丰富和浅埋藏的水文地质条件下相对较高。地下水的DIC在湖滨平原砂砾石层、淤泥质砂层潜水和水量中等的水文地质条件下受冻融期影响较大,DOC在基岩裂隙水和水量贫乏的水文地质条件下受冻融期影响较大。湖水的DIC和DOC均远高于河水和地下水。河水的DIC在融化期和冻结期均低于地下水,DOC在融化期高于地下水,在冻结期低于地下水。     

A 24 h investigation of the hydrogeochemistry of baseflow and stormwater in an urban area impacted by mining: Butte,Montana

Changes in water quality during a storm event were continuously monitored over a 24 h period at a single location along an urban stormwater drain in Butte, Montana. The Butte Metro Storm Drain (MSD) collects groundwater baseflow and stormwater draining Butte Hill, a densely populated site that has been severely impacted by 130 years of mining, milling, and smelting of copper‐rich, polymetallic mineral deposits. On the afternoon of 26 June 2002, a heavy thunderstorm caused streamflow in the MSD to increase 100‐fold, from 0·2 ft³ s⁻¹ to more than 20 ft³ s⁻¹. Hourly discharge and water quality data were collected before, during, and following the storm. The most significant finding was that the calculated loads (grams per hour) of both dissolved and particulate copper passing down the MSD increased more than 100‐fold in the first hour following the storm, and remained elevated over baseline conditions for the remainder of the study period. Other metals, such as zinc, cadmium, and manganese, showed a decrease in load from pre‐storm to post‐storm conditions. In addition to the large flush of copper, loads of soluble phosphorus increased during the storm, whereas dissolved oxygen dropped to low levels (<2 mg l⁻¹). These results show that infrequent storm events in Butte have the potential to generate large volumes of runoff that exceed Montana water quality standards for acute exposure of aquatic life to copper, as well as depressed levels of dissolved oxygen. This study has important implications to ongoing reclamation activities in the upper Clark Fork Superfund site, particularly with respect to management of storm flow, and may be applicable to other watersheds impacted by mining activities. Copyright © 2005 John Wiley & Sons, Ltd.     

The effect of drawdown on suspended solids and phosphorus export from Columbia Lake,Waterloo, Canada

This study examines the effect of drawdown on the timing and magnitude of suspended solids and associated phosphorus export from a 12 ha reservoir located in an urbanized watershed in southern Ontario, Canada. Water level in Columbia Lake was lowered by 1·15 m over a 2‐week period in November 2001. The total phosphorus (TP) concentrations ranged from 63 to 486 µg L^?1 in Columbia Lake and 71 to 373 µg L^?1 at its outflow. All samples exceeded the Provincial Water Quality Objective of 30 µg TP L^?1. Outflow concentrations of suspended solids and TP increased significantly with decreasing lake level and were attributed to the resuspension of cohesive bottom sediments that occurred at a critical threshold lake level (0·65 m below summer level). Suspended solids at the outflow consisted of flocculated cohesive materials with a median diameter (D₅₀) of c. 5 µm. Particulate organic carbon accounted for 8·5% of the suspended solids export by mass. A total mass of 18·5 t of suspended solids and 62·6 kg TP was exported from Columbia Lake, which represents a significant pulse of sediment‐associated P to downstream environments each autumn during drawdown. The downstream impacts of this release can be minimized if the water level in Columbia Lake is lowered no more than 0·5 m below summer levels. Copyright © 2004 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.     

Continuous fluorescence assessment of organic matter variability on the Bournbrook River,Birmingham, UK

Continuous monitoring of dissolved organic matter (DOM) character and concentration at hourly resolution is rare, despite the importance of analysing organic matter variability at high‐temporal resolution to evaluate river carbon budgeting, river water health by detecting episodic pollution and to determine short‐term variations in chemical and ecological function. The authors report a 2‐week experiment performed on DOM sampled from Bournbrook, Birmingham, UK, an urban river for which spectrophotometric (fluorescence, absorbance), physiochemical (dissolved organic carbon [DOC], electrical conductivity, pH) and isotopic (D/H) parameters have been measured at hourly frequency. Our results show that the river had sub‐daily variations in both organic matter concentration and characteristics. In particular, after relatively high‐magnitude precipitation events, organic carbon concentration increased, with an associated increase in intensity of both humic‐like and tryptophan‐like fluorescence. D/H isotopic ratio demonstrates different hydrological responses to different rainfall events, and organic matter character reflects this difference. Events with precipitation < 2 mm typically yielded isotopically heavy water with relatively hydrophilic DOM and relatively low specific absorbance. Events with precipitation > 2 mm had isotopically lighter water with higher specific absorbance and a decrease in the proportion of microbially derived to humic‐like fluorescence. In our heavily urbanized catchment, we interpret these signals as one where riverine DOM is dominated by storm sewer‐derived ‘old’ organic matter at low‐rainfall amounts and a mixed signal at high‐precipitation amounts where ‘event’ surface runoff‐derived organic matter dominate during storm sewer and combined sewer overflow routed DOM. Copyright © 2009 John Wiley & Sons, Ltd.     

气候变暖对湖泊热力及溶解氧分层影响研究进展

气候变暖对湖泊物理、化学、生物和生态系统有着复杂而深刻的直接和间接影响,而具体影响随研究区域和水体表现不尽相同。气候变暖通过改变湖泊热力和溶解氧分层进而影响湖泊生物过程和生态系统结构与功能。从全球湖泊变暖趋势、长期缓慢气温上升、极端高温事件以及气候情景模拟等方面详细综述了气候变暖对湖泊热力及溶解氧分层影响的研究进展。研究表明,全球不同区域湖泊均存在不同程度的变暖趋势;长期缓慢气温上升和短期极端高温均会造成湖泊热力分层提前,分层结束推迟,分层时间延长,混合层和温跃层深度下降,以及热稳定性增加;相伴随的是溶解氧扩散深度和氧跃层深度明显下降,加剧了湖泊底部好氧和厌氧环境。除了这种直接影响外,气候变暖引起的流域降水、入湖物质的变化以及风速的变化也会对湖泊热力和溶解氧分层产生许多间接的影响,因此未来仍然需要更多的实验证据、经验和数值模型来验证和预测气候变暖对湖泊热力及溶解氧分层的影响。     

Variations in dissolved CO2 and CH4 in a first‐order stream and catchment: an investigation of soil–stream linkages

Spatial and seasonal variations in CO₂ and CH₄ concentrations in streamwater and adjacent soils were studied at three sites on Brocky Burn, a headwater stream draining a peatland catchment in upland Britain. Concentrations of both gases in the soil atmosphere were significantly higher in peat and riparian soils than in mineral soils. Peat and riparian soil CO₂ concentrations varied seasonally, showing a positive correlation with air and soil temperature. Streamwater CO₂ concentrations at the upper sampling site, which mostly drained deep peats, varied from 2·8 to 9·8 mg l^?1 (2·5 to 11·9 times atmospheric saturation) and decreased markedly downstream. Temperature‐related seasonal variations in peat and riparian soil CO₂ were reflected in the stream at the upper site, where 77% of biweekly variation was explained by an autoregressive model based on: (i) a negative log‐linear relationship with stream flow; (ii) a positive linear relationship with soil CO₂ concentrations in the shallow riparian wells; and (iii) a negative linear relationship with soil CO₂ concentrations in the shallow peat wells, with a significant 2‐week lag term. These relationships changed markedly downstream, with an apparent decrease in the soil–stream linkage and a switch to a positive relationship between stream flow and stream CO₂. Streamwater CH₄ concentrations also declined sharply downstream, but were much lower (<0·01 to 0·12 mg l^?1) than those of CO₂ and showed no seasonal variation, nor any relationship with soil atmospheric CH₄ concentrations. However, stream CH₄ was significantly correlated with stream flow at the upper site, which explained 57% of biweekly variations in dissolved concentrations. We conclude that stream CO₂ can be a useful integrative measure of whole catchment respiration, but only at sites where the soil–stream linkage is strong. Copyright © 2004 John Wiley & Sons, Ltd.