杭州西湖沉积物磷分析及释放风险

本研究以杭州西湖的茅家埠、小南湖以及乌龟潭等3个子湖中的沉积物为研究对象,研究其中沉积物磷赋存形态,通过对沉积物磷吸附指数(phosphorus sorption index, PSI)与磷吸附饱和度(phosphorus saturation, DPS)进行测定与计算并根据两者对西湖沉积物磷的释放风险进行了客观评估.对沉积物风险分析表明:杭州西湖沉积物呈还原态,表现出强氧化性;沉水植物的生长会对沉积物的氧化还原电位产生影响,沉水植物盖度越大,沉积物氧化还原电位越高,氧化性越强;沉积物磷污染状况严重,沉积物中磷的吸附容量主要与其中活性铁铝氧化物的含量有关;杭州西湖不同区域的沉积物磷的吸附指数有较大的不同,主要与区域的生态化逆境相关;受各种相关因素影响,杭州西湖沉积物磷的释放处于中度偏轻的风险状态.     

武汉东湖近代沉积物中总氮、总磷与生物硅沉积与营养演化的动态过程

选择富营养化程度较高的武汉东湖作为研究对象,于2011年对其中4个子湖湖心的沉积物进行了采集,并分析了沉积物中总氮、总磷与生物硅含量。结果表明：对照东湖沉积速率（约0.33 cm·a-1）,在底层41～50 cm（1860—1890年）与31～40 cm（1890—1920年）,东湖4处子湖氮、磷、硅基本为湖泊自然沉积;在中层21～30 cm（1920—1950年）,人类活动有所增强,沉积有所变化;表层沉积物0～10 cm（1980—2010年）、11～20 cm（1950—1980年）中氮、磷、硅沉积普遍上升,这一时期对应着东湖人类干扰活动的普遍增加。对东湖4个子湖的沉积物氮、磷与硅的对比研究表明：人类活动增加了对东湖氮、磷的排放,促进了东湖硅藻的生长及硅的消耗,东湖不同子湖之间氮、磷、硅的沉积存在着明显差异,这可能与人类活动的影响差异有关。     

武汉东湖近代沉积物中总氮、总磷与生物硅沉积与营养演化的动态过程

选择富营养化程度较高的武汉东湖作为研究对象,于2011年对其中4个子湖湖心的沉积物进行了采集,并分析了沉积物中总氮、总磷与生物硅含量。结果表明:对照东湖沉积速率(约0.33 cm·a-1),在底层41～50 cm(1860—1890年)与31～40 cm(1890—1920年),东湖4处子湖氮、磷、硅基本为湖泊自然沉积;在中层21～30 cm(1920—1950年),人类活动有所增强,沉积有所变化;表层沉积物0～10 cm(1980—2010年)、11～20 cm(1950—1980年)中氮、磷、硅沉积普遍上升,这一时期对应着东湖人类干扰活动的普遍增加。对东湖4个子湖的沉积物氮、磷与硅的对比研究表明:人类活动增加了对东湖氮、磷的排放,促进了东湖硅藻的生长及硅的消耗,东湖不同子湖之间氮、磷、硅的沉积存在着明显差异,这可能与人类活动的影响差异有关。     

黄渤海表层沉积物中正构烷烃和甾醇的分布及来源研究

在黄海、渤海湾和莱州湾采集64个表层沉积物样品,分析正构烷烃（C15～C33）和甾醇（菜子甾醇、菜油甾醇、谷甾醇和豆甾醇）的质量分数和分子组合特征,探讨其来源,比较物质来源的空间差异。结果表明：（1）黄海表层沉积物中类脂生物标志物主要呈现陆源和海源共同影响的特征,其中北黄海以陆源输入为主,高碳数正构烷烃（〉C24）具有明显的奇碳优势,陆源高等植物的贡献较大;南黄海陆源输入与海洋自身贡献相当;渤海湾与莱州湾接受来自河流的大量陆源物质;（2）来源于陆源高等植物的甾醇（包括菜油甾醇、谷甾醇和豆甾醇）在黄海表层沉积物中的质量分数远小于渤海湾和莱州湾,但指示硅藻来源的菜子甾醇在整个研究区域均具有较高的质量分数。     

黄渤海表层沉积物中正构烷烃和甾醇的分布及来源研究

在黄海、渤海湾和莱州湾采集64个表层沉积物样品,分析正构烷烃(C15～C33)和甾醇(菜子甾醇、菜油甾醇、谷甾醇和豆甾醇)的质量分数和分子组合特征,探讨其来源,比较物质来源的空间差异。结果表明:(1)黄海表层沉积物中类脂生物标志物主要呈现陆源和海源共同影响的特征,其中北黄海以陆源输入为主,高碳数正构烷烃(>C24)具有明显的奇碳优势,陆源高等植物的贡献较大;南黄海陆源输入与海洋自身贡献相当;渤海湾与莱州湾接受来自河流的大量陆源物质;(2)来源于陆源高等植物的甾醇(包括菜油甾醇、谷甾醇和豆甾醇)在黄海表层沉积物中的质量分数远小于渤海湾和莱州湾,但指示硅藻来源的菜子甾醇在整个研究区域均具有较高的质量分数。     

武汉严东湖近代沉积物中总氮、总磷与生物硅沉积及营养演化的动态过程

选择武汉近郊一中型浅水湖泊——严东湖为研究对象,对其进行了2个柱状沉积物的总氮、总磷、生物硅含量测试。结果表明：严东湖表层沉积物中总氮、生物硅含量总体均有所上升,而总磷近代含量有所下降。近代以来,硅藻的生长消耗了水体大量的硅与磷,表现为生物硅含量的显著上升,严东湖的营养程度有所上升。硅藻的生长与沉积影响到湖泊的沉积系统与过程,使营养盐比例与结构发生了变化,导致严东湖水体出现硅限制。     

凡口铅锌矿湿地系统沉积物中重金属的分布

研究了用于处理凡口铅锌矿选矿废水的宽叶香蒲(Typha latifolia)人工湿地系统沉积物中重金属Pb、Zn、Cu和Cd的分布。沉积物略呈碱性,在各层沉积物中,DTPA-Zn质量分数高于DTPA-Pb质量分数。冬季(11~12月)湿地系统中3个处理池进水口的沉积物结合水中的Pb、Zn、Cu和Cd质量分数与春季(1~3月)的相比较,有显著的差异。湿地处理系统中Pb、Zn、Cu和Cd主要沉积在表层土壤中;但3个处理池入水口和出水口不同深度的沉积物pH值没有显著差异(p<0.05),表明pH值与重金属含量并不存在相关性。     

汕头红树林湿地表层沉积物环境因子对PAHs分布的影响

为了探明红树林湿地表层沉积物环境因子对多环芳烃分布的影响,野外采集了汕头红树林湿地表层沉积物样品,实验室内有机溶剂提取、氧化铝硅胶柱净化和气质联用分析了沉积物多环芳烃的质量分数、CHN元素仪分析了沉积物有机碳和黑碳的质量分数、激光粒度仪分析了沉积物的粒级组成,研究了沉积物有机碳、黑碳和粒度等各环境因子与多环芳烃的相关性.结果表明:有机碳与2～3环、4环和总多环芳烃的质量分数显著相关(P<0.05),表明表层沉积物有机碳的质量分数对PAHs的分布产生了显著的影响;黑碳与2～3环、4环、5～6环和总多环芳烃的质量分数显著相关(P<0.01),表明表层沉积物黑碳的质量分数对PAHs的分布产生了显著的影响;粘粒与2～3环多环芳烃的质量分数显著相关(P<0.05),与4环、5～6环和总多环芳烃的质量分数显著相关(P<0.01),表明表层沉积物粘粒的质量分数对PAHs的分布也产生了显著的影响;多元线性逐步回归分析显示,各回归方程黑碳的偏回归系数值都是最大,沉积物黑碳的质量分数对多环芳烃的质量分数贡献最大,表明黑碳是多环芳烃分布的主要影响因素.     

柘林湾养殖区表层沉积物多环芳烃的分布、来源及风险评价

对柘林湾养殖区表层沉积物样品中多环芳烃(PAHs)进行了定量分析,采用风险商(RQ)和沉积物质量标准(SQG)评价了沉积物中PAHs的生态风险和各位点的综合生态风险,初步分析了沉积物中PAHs的来源以及沉积物中PAHs与沉积物相关参数的相关性,为有机污染物污染控制和环境管理等提供科学依据。结果表明,柘林湾表层沉积物各位点∑PAHs的质量分数为71.03~148.64 ng·g~(-1),平均值为107.87 ng·g~(-1),各种PAHs的质量分数为0.50~18.49 ng·g~(-1)。PAHs的RQERM值和各位点的m ERM-Q值均小于0.1,RQERL值绝大部分都小于0.1,表明该养殖区各PAHs在各位点处的生态风险不明显。柘林湾养殖区表层沉积物中PAHs的来源主要是木柴、煤等燃烧来源与石油燃烧来源的混合,这可能是人类活动与海航交通运输过程石油排放导致的结果。TOC、间隙水TOC、Ca的含量以及颗粒物粒径大小对PAHs积累和富集皆有中等以上程度的相关,且相近分子量PAHs之间存在显著相关。     

渤海湾海岸带表层沉积物中黑碳的分布特征

在渤海湾西海岸潮间带、近海和主要河流采集了85个表层沉积物样品,对黑碳（BC）的质量分数及其分布规律进行了研究,并探讨了BC与沉积物粒度的关系。结果表明：（1）渤海湾海岸带表层沉积物中BC的平均质量分数为（0.65±0.42）mg·g^-1,占总有机碳的比例为16.8%±7.5%,均高于我国其它海岸带;（2）潮间带沉积物中BC的质量分数存在明显的南北分区差异（以天津港码头为界）,北区（0.92mg·g^-1）比南区（0.22mg·g^-1）平均高4倍以上;近海和河流样品BC的质量分数也有一定程度的＂北高南低＂趋势,表明BC在海岸带运移扩散的继承性,河流输入可能是主要途径;（3）潮间带沉积物粒度表现为＂北区细＂（以粘土质粉砂主）而＂南区粗＂（以砂为主）,反映两个区域的水动力条件和沉积环境不同,是造成BC质量分数区域差异的主要原因。     

Vertical and spatial distribution of biogenic silica in the sediment of the gulf of Riga,Baltic Sea

The vertical and spatial concentration trends of biogenic silica (BSi) were investigated in a variety of sediment types from the Gulf of Riga. These trends were compared with the concentration of organic carbon to examine how variations in the mass sedimentation and the dissolution rate of BSi versus bacterially mediated oxidation of organic matter affect the distribution of BSi in different environments. The effects of important physical and biogeochemical factors on the distribution of BSi have also been examined.

The concentration of BSi in the surface sediment at accumulation bottoms ranges between 0.8–1.5 mmol/g with an average concentration of 1.1 mmol/g. This is about two times the concentration that has been reported in similar sediments in the open Baltic proper. Much lower concentrations were measured in erosion and transitional areas; on average around 0.2 and 0.6 mmol/g, respectively.

A comparison between recent sedimentation rate measurements (²¹⁰Pb) and concentrations of BSi within different accumulation bottoms suggests an approximate inverse relationship with each other. The importance of variation in the sedimentation rate on the surface BSi concentration is supported by the fact that higher C_org/BSi ratios are found in periphery accumulation zones close to transition areas (larger supply of carbon rich allochthonous material that dilutes settled amounts of BSi) than at accumulation bottoms in the central part of the Gulf. The C_org/BSi ratio in the sediment is always lower than in living siliceous algae which shows that the microbial degradation of organic carbon is always greater than the inorganic dissolution of BSi, irrespective of the assemblage of silica and non‐silica species.

The general vertical concentration pattern at accumulation sites showed a decreased concentration with increased depth down to 2–6 cm below seafloor where the concentration gradually equalizes. The concentration in the equalizing zone is on average about 20% lower than in the uppermost centimeter. This implies that the main part of the BSi entering the accumulation bottoms is permanently buried and that a great amount of silica already has been released during halmyrolysis. The spatial and vertical BSi trends at sites in transitional and erosional areas reflects prevailing sedimentation conditions with a low concentration in sections with a dominance of sand and gravel (no deposition of fine material) and a higher concentration in the sections containing stiff glacial clay (former accumulation area).

The average annual burial amount of BSi in the Gulf has been estimated to be around 50 000 tons of which most is buried in accumulation bottoms outside the central muddy part of the Gulf. The buried amount is about 60% of the annual river load of silica.     

白洋淀沉积物中磷的存在形态及垂直变化规律研究

湖泊沉积物中磷的含量及其形态分布是影响湖泊营养化进程的极为重要因素,对研究湖泊营养化等环境问题具有重要意义。采用化学连续提取分析法,对白洋淀环淀中村水域不同地点的沉积物中磷的形态及其在垂直方向上的变化进行了研究。结果表明,研究区域内,环淀中村水域表层沉积物总磷（TP）质量分数在544.424～608.197mg·kg-1之间,无机磷（IP）是沉积物中磷的主要形态,有机磷（OP）质量分数较小,约占10%～27%,无机磷中钙磷（Ca-P）占的比例相对较大,在质量分数上约占75.8%～94.1%。从各形态磷质量分数的变化范围来看,Ca-P〉OP〉Fe/Al-P;人类活动对湖泊沉积物中磷的形态及其水平和垂向变化影响很大。     

沉积物对菲和五氯酚的吸附性能

研究了菲和五氯酚（PCP）在五种沉积物的吸附解吸行为，菲和PCP在各沉积物上的吸附和解吸都是较快的过程。均能在8h内达到平衡，吸附和解吸结果表明，高有机质含量的沉积物对菲和PCP的吸附和持留能力都较强，菲和PCP在各沉积物中的吸附系数跟沉积物的有机质含量呈线性正相关。等温吸附结果表明，低有机质含量的三种沉积物比有机质含量较高的两种沉积物呈更好的线性关系。不同沉积物对菲和PCP的吸附性能差异跟沉积物的有机质含量密切相关。     

洞庭湖主要入湖口表层沉积物重金属分布特征与生态风险评价

尽管针对洞庭湖沉积物中重金属的研究工作较多,但缺乏针对其主要入湖口的研究。基于2014年12月和2015年6月对洞庭湖主要入湖口表层沉积物中重金属调查,分析了重金属含量的时空分布特征,并采用一致性沉积物质量基准法对其生态风险进行了评价。结果表明,Cd、Hg、As、Cu、Pb和Zn的平均含量分别为3.27、0.190、27.10、39.8、38.0和157.8 mg·kg-1,其大小顺序为ZnCuPbAsCdHg,Cd和As含量出现超过土壤环境质量三级标准的现象,是主要的重金属污染物。Cd、As、Pb和Zn等4种重金属含量的最高值均出现在湘江入湖口,Cu含量的最高值出现在资水入湖口,Hg含量以沅江入湖口最高,除Pb外,其他5种重金属在湘江和资水入湖口的含量均大于平均值,表明湘江和资水入湖口污染较为严重;汛期与非汛期6种重金属的含量均无显著性差异(P0.05)。6种重金属生态风险大小顺序为AsCdZnPbCuHg,各入湖口生态风险大小顺序为湘江入湖口资水入湖口沅江入湖口汨罗江入湖口澧水入湖口长江"三口"新墙河入湖口,其中湘江和资水入湖口为较高生态风险,其他入湖口为较低生态风险。入湖河流是洞庭湖湖体沉积物重金属污染的主要来源,在一定程度上,入湖河流沉积物中重金属的含量对洞庭湖湖体沉积物中重金属污染状况起着决定性作用,因此,洞庭湖流域重金属污染防控应以入湖河流为主,其中尤以湘江和资水为重点。     

Revealing the factors affecting occurrence and distribution of polycyclic aromatic hydrocarbons in water and sediments of Lake Baikal and its tributaries

The concentrations of polycyclic aromatic hydrocarbons (PAH), total carbon (TC), total organic carbon (TOC), total nitrogen (TN) and dissolved inorganic nitrogen (DIN) in water and sediments of Lake Baikal and its tributaries were measured. It was found that according to existing water and sediment quality standards limiting permissible PAH concentrations, both surface waters and sediments in Lake Baikal watershed can be considered as unpolluted with PAHs compounds. Nevertheless, the spatial distribution of PAH concentrations in lake water indicates the existence of some point PAH sources in and around the lake. These sources were natural oil seeps and communal facilities such as residential coal-fired and oil-fired boilers. It was observed that concentrations of PAHs in both water and sediments are controlled by organic matter content and organic matter mineralisation degree, as indicated by PAH-to-carbon and nitrogen-to-carbon ratios respectively. It was found that PAH/TOC and PAH/TC ratios characterise PAH loading on water and sediments respectively, whereas DIN/TOC and TN/TC ratios characterise self-purification of water and sediments respectively. It was proved that PAH/TOC and DIN/TOC ratios can be used as tracers to evaluate the PAH contributions from tributaries to Lake Baikal.     

广州市流花湖表层底泥磷的形态与生物可利用性

应用经改进的Psenner连续提取法对广州市流花湖表层底泥中的磷进行了连续提取和测定。结果表明,流花湖底泥中总磷含量在1.28~2.15 mg/g,流花湖总磷含量最高在L2点,最低在L3点。湖泊表层底泥总磷主要由金属氧化物结合态磷、有机磷和钙结合态磷组成,可还原态磷和弱吸附态磷仅占很少部分。不同形态磷的含量顺序是金属氧化物结合态磷NaOH-P>有机磷Org-P>钙结合态磷HCl-P>可还原态磷BD-P>弱吸附态磷NH4Cl-P。底泥中生物可利用性磷的含量达0.76~1.00 mg/g,平均含量为0.91 mg/g,占总磷的45.47%~64.71%。说明流花湖底泥的磷有较好的生物可利用性,将为水体藻类大量繁殖提供潜在的有利条件,因此在湖泊治理恢复过程中,应该采样有效的措施来控制底泥磷的内源释放。     

Denitrification mitigates N flux through the stream-floodplain complex of a desert city

The Indian Bend Wash (IBW) flood-control project relies on a greenbelt to carry floods through Scottsdale, Arizona, USA. The greenbelt is characterized by a chain of shallow artificial lakes in a larger floodplain of irrigated turf, which has been protected from encroaching urban development. As such, this urban stream-floodplain complex can be divided into three subsystems: artificial lakes, channelized stream segments, and floodplain. We conducted experiments to evaluate which, if any, of these subsystems were important sites of denitrification, and to explore factors controlling denitrification rates. Denitrification enzyme activity (DEA) bioassays were conducted on sediments from eight lake and six stream segments as well as soil samples from eight floodplain transects. Mass-specific potential denitrification rates were significantly higher in lakes than in streams or floodplains. Nutrient limitation bioassays revealed that nitrate (NO3-) limited denitrification in lake sediments, a surprising finding given that NO3(-)-rich groundwater additions frequently raised lake NO3(-) concentration above 1 mg N/L. Experiments on intact lake cores suggested that denitrification was limited by the rate NO3(-) diffused into sediments, rather than its availability in overlying water. Floodplain denitrification was limited by water content, not NO3(-) or C, and irrigation of soils stimulated denitrification. We constructed a N budget for the IBW stream-floodplain complex based on our experimental results. We found that both lakes and floodplains removed large quantities of N, with denitrification removing 261 and 133 kg N ha(-1) yr(-1) from lake sediments and floodplain soils, respectively, indicating that lakes are hotspots for denitrification. Nevertheless, because floodplain area was >4.5 times that of lakes, floodplain soils removed nearly 2.5 times as much N as lake sediments. Given the desert's low annual precipitation, a finding that floodplain soils are active sites of denitrification might seem implausible; however, irrigation is common in urban landscapes, and it elevated annual denitrification in IBW. Based on our results, we conclude that construction of artificial lakes created hotspots while application of irrigation water created hot moments for denitrification in the stream-floodplain complex, demonstrating that management decisions can improve the ability of urban streams to provide critical ecosystem services like N retention.     

河北省衡水湖沉积物中汞的分布特征及生态风险

衡水湖是华北平原上第一个国家级内陆淡水湖泊湿地类型的自然保护区,为了解衡水湖沉积物中汞的分布特征及生态风险,于2013年8月在衡水湖采集了5根柱状沉积物,对其中的总汞、甲基汞、孔隙水溶解态汞、有机质、pH以及含水率进行了分析。结果表明,衡水湖沉积物中总汞的平均含量为22.5 ng·g-1,低于全国及河北省表层土壤背景值。但表层沉积物汞含量明显高于底层,说明近年来的外源汞输入对湖泊汞负荷产生了一定影响,且靠近湖泊东部106国道的采样点汞含量明显高于湖泊中西部的采样点,暗示交通运输等人为活动是该湖泊的一个重要汞输入源。利用潜在生态危害指数法进行评估,显示汞的生态风险较低,说明现阶段衡水湖的沉积物汞浓度不会对生态环境产生不利影响。