The Water Fluxes of the Yellow River to the Sea in the Past 50 Years, in Response to Climate Change and Human Activities

Since the 1970s, the water fluxes to the sea of the Yellow River have declined significantly. Based on data of precipitation, air temperature, the measured and “natural” river flow, the water diversion and consumption, and the areas of erosion and sediment control measures over the drainage basin, water fluxes to the sea of the Yellow River are studied in relation with the influences of changing climate and human activities. The Yellow River basin can be divided into different water source areas; multiple regression indicates that the variation in precipitation over different water source areas has different effect on water fluxes to the sea. In the period between 1970 and 1997, averaged air temperature over the whole Yellow River increased by about 1.0°C, from 16.5°C to 17.5°C, a factor that is negatively correlated with the water yield of the Yellow River. Water diversion and consumption has sharply increased and resulted in a significant decline in the water fluxes to the sea. Since the 1960s, erosion and sediment control measures have been practiced over the drainage basin. This factor, to a lesser degree, is also responsible for the decrease in water fluxes to the sea. A multiple regression equation has been established to estimate the change in water fluxes to the sea caused by the changes in precipitation, air temperature, water diversion and consumption, erosion, and sediment control measures, indicating that the contribution of water diversion and consumption to the variation in annual water flux to the sea is 41.3%, that of precipitation is 40.8%, that of temperature is 11.4%, and that of erosion and sediment control measures is 6.5%.     

HISTORICAL TRENDS IN SEDIMENTATION RATES AND SEDIMENT PROVENANCE,FAIRFIELD LAKE,WESTERN NORTH CAROLINA1

Sedimentation rates and sediment provenance were examined for lacustrine sediments deposited in Fairfield Lake, western North Carolina, during the past 111 years. Stratigraphic, radionuclide, and cartographic data indicate that sedimentation rates have increased several fold during the past three decades in response to localized development. The magnitude of increased sedimentation was surprising given limited development within the basin: 0.12 to 0.68 buildings/ha in 2000 in those parts directly delivering sediment to the dated cores. Thus, the analysis illustrates the potential sensitivity of watersheds in the southern Appalachians to changes in land cover. An approach that combined geochemical fingerprinting with sediment mixing models was subsequently evaluated to determine its ability to accurately estimate the contribution of sediment from (1) major bedrock formations that underlie the watershed and (2) potential sources associated with four land cover categories. Sediment sources in both analyses proved difficult to geochemically fingerprint to greater than 90 percent accuracy using data on acid‐soluble metals and selected isotopes of lead (Pb). The relative contributions of sediment from delineated sources, estimated by the mixing models, generally corresponded with known temporal and spatial patterns of land cover. However, the models were plagued by two significant problems — the chemical alteration of sediments as they were transported through upland streams to depositional sites within the lake and the loss of elemental mass. Thus, future investigations using the fingerprinting approach in this area of intense weathering, and presumably others, will need to modify the existing methods to more accurately elucidate changes in sediment provenance related to development.     

DEVELOPMENT OF EMPIRICAL,GEOGRAPHICALLY SPECIFIC WATER QUALITY CRITERIA: A CONDITIONAL PROBABILITY ANALYSIS APPROACH1

The need for scientifically defensible water quality standards for nonpoint source pollution control continues to be a pressing environmental issue. The probability of impact at differing levels of nonpoint source pollution was determined using the biological response of instream organisms empirically obtained from a statistical survey. A conditional probability analysis was used to calculate a biological threshold of impact as a function of the likelihood of exceeding a given value of pollution metric for a specified geographic area. Uncertainty and natural variability were inherently incorporated into the analysis through the use of data from a probabilistic survey. Data from wadable streams in the mid‐Atlantic area of the U.S. were used to demonstrate the approach. Benthic macroinvertebrate community index values (EPT taxa richness) were used to identify impacted stream communities. Percent fines in substrate (silt/clay fraction, > 0.06 mm) were used as a surrogate indicator for sedimentation. Thresholds of impact due to sedimentation were identified by three different techniques, and were in the range of 12 to 15 percent fines. These values were consistent with existing literature from laboratory and field studies on the impact of sediments on aquatic life in freshwater streams. All results were different from values determined from current regulatory guidance. Finally, it was illustrated how these thresholds could be used to develop criterion for protection of aquatic life in streams.     

三峡蓄水期间汉丰湖消落区营养状态时间变化

为探明三峡蓄水后汉丰湖消落区水质营养状态的变化特征,于2013年10月至2014年2月对水质进行连续观察,测定了水质物理参数、营养盐与叶绿素(Chl-a)的质量浓度.结果表明,水体中营养盐与Chl-a质量浓度的增加,在淹水后营养程度有升高现象,2014年2月与2013年10月相比,TN、TP、高锰酸盐指数与Chl-a质量浓度分别增加了4.7、1.0、0.2、3.27倍,TN、TP质量浓度均超过藻类生长限值,随滞留时间延长易造成水体富营养化,应引起重视.Chl-a单因子评价反映出水质由贫营养向富营养演变.TN/TP结果表明,TN、TP分别在不同时间内制约着藻类的生长;2013年10~12月与2014年2月,藻类生长受TN限制;2014年1月,藻类生长受TP限制.Chl-a与p H、DO、NH+4-N、NO-3-N、TN、高锰酸盐指数及TP呈显著正相关,而与SD、水温呈显著负相关;蓄水期间,水质受到了同一污染源的影响.因子分析结果表明,汉丰湖消落区水质主要受p H、DO、NO-3-N、TN的影响,同时Chl-a、TP、NH+4-N与好氧性有机物的污染不可忽视;在蓄水稳定初期水体具有自净能力,随蓄水滞留时间的延长,水质污染程度整体上呈现逐步恶化的趋势,应加以控制;三峡蓄水期间,南河、东河营养程度相对较高,应加强治理.     

应用相平衡分配法建立湘江衡阳段沉积物重金属质量基准

采集湘江衡阳段29个站点的表层沉积物样品,测定沉积物中4种重金属(Cu、Pb、Zn和Cd)含量及赋存形态、以及孔隙水中重金属含量,根据相平衡分配法的基本理论,考虑参与沉积物-水相平衡分配的重金属组成,实测法计算重金属的沉积物-水相平衡分配系数(Kp),分别引用美国EPA制定保护水生生物不受重金属慢性毒性影响的基本连续浓度(CCC)和我国地表水环境质量标准(GB 3838-2002)Ⅰ类水质标准,建立两种湘江衡阳段沉积物重金属质量基准(SQC)进行对比分析,其中基于美国CCC建立的湘江衡阳段沉积物重金属质量基准与国内外研究成果相比可比性较好,4种重金属(Cu、Pb、Zn和Cd)的SQC值分别为64.62、55.57、1 360.40和2.34μg.g-1,此SQC具有保护长期生活于沉积物中的底栖生物不受重金属慢性毒性影响的意义.通过单因子评价法将湘江衡阳段沉积物中重金属总量与沉积物质量基准值(SQC)进行比较,结果表明,湘江衡阳段沉积物中Cd和Pb含量水平对底栖生物具有较大的慢性毒性影响,Cd污染不容忽视.     

“引江济太”过程中长江-望虞河-贡湖氮、磷输入特征研究

为了解"引江济太"调水过程中长江、望虞河对贡湖营养盐输入特征,于2013年8月和2013年12月引水期间对20个采样点各形态N、P质量浓度的沿程和时间变化以及百分含量占比进行研究.结果表明,两个不同的引水期,长江-望虞河-贡湖段水体各形态N、P沿程和时间变化均表现不一:长江引水经望虞河入贡湖后,水体NO-2-N、NO-3-N、NH+4-N和TN质量浓度均较长江和望虞河段有不同程度的降低,而贡湖段DON质量浓度显著高于长江和望虞河段,但长江-望虞河段水体各形态N中NO-3-N质量浓度最高.长江和望虞河TP质量浓度总体表现平稳,而各形态P质量浓度在两个引水时期内有所变化.从时间变化来看,2013年8月水体的DON和TP质量浓度总体上高于12月;而NO-3-N和DOP质量浓度总体上低于12月.总体来说,两个引水时期内,NO-3-N和TPP是望虞河经长江引水的主要N、P形态;而贡湖经望虞河水体输入的N、P主要形态分别为NO-3-N、PO3-4-P和TPP.     

西大海湖沉积物营养盐垂直分布特征变化分析

通过对西大海湖心柱状沉积岩芯有机质(OM)、总氮(TN)、总磷(TP)、磷形态和粒度指标的测试和分析,探讨其垂向分布特征及影响因素.结果表明,营养盐中OM、TN和TP的含量分别为0.633%~2.756%、0.150%~0.429%和648.00~1 480.67 mg·kg-1.Ca-P是TP的主要部分,占TP含量66.04%.1843~1970年间,Ca-P、IP、OM含量变化较小,Fe/Al-P、OP、TP、TN含量波动较大;1970~1996年间,Ca-P、IP、TP含量变化均呈减小趋势,Fe/Al-P、OP、OM含量不同程度上先减少后增加,TN波动较大;1996~2009年营养元素含量相对波动较大,Fe/Al-P、OP和OM的平均含量是3个阶段中最高的.西大海湖沉积岩芯营养元素污染来源以工业废水、生活污水和化肥农药的流失为主.沉积物中C/N比值显示有机质主要来源于水生生物.沉积物粒度组成以黏土和细粉砂为主.相关性研究表明,Ca-P、IP与TP均呈显著的正相关关系,表明Ca-P对IP、TP的增长贡献大.     

太湖表层水体及沉积物中双酚A类似物的分布特征及潜在风险

本研究对太湖表层水和沉积物中7种双酚A类似物(BPs)的浓度水平及分布特征进行了调查,并对其潜在的风险进行了评估.结果表明太湖表层水中双酚F(BPF)、双酚S(BPS)和双酚A(BPA)为主要的BPs组分;沉积物中BPA对BPs总浓度的贡献率最高,其次为BPF和BPS,且与沉积物中TOC含量具有显著的正相关;BPA、BPF和BPS在表层水和沉积物中的高浓度水平均分布在太湖入湖支流(采样点S4~S10).风险评估表明BPs的联合毒性风险熵表现出低生态风险,且对人体不具有明显的健康风险.     

夏季太湖CDOM光学特性空间差异及其来源解析

为进一步探究夏季太湖CDOM（有色溶解性有机质）光学特性在空间分布上的差异性与其来源的关系,对其紫外-可见吸收及三维荧光光谱特性进行了分析研究,在此基础上进一步分析了CDOM吸尘系数及其荧光组分（C1、C2、C3、C4）强度和各水质参数间的相关性.结合主成分分析法探讨了CDOM的来源以及与各参数指标[ρ（DOC）除外]之间的来源关系.结果表明:CDOM吸收系数α（355）、S值（光谱斜率）变化范围分别为3.27~8.27 m-1和0.011~0.021 nm-1;太湖西部、北部及南部湖区CDOM丰度较大,S值较低,受陆源输入的影响较为明显.CDOM的三维荧光光谱揭示其中含有两种类蛋白质组分C1和C2以及类腐殖质组分C3和C4,并且以类蛋白质组分为主.此外,大部分采样点的荧光指数（FI）为1.70~2.01,自生源指数（BIX）大于1,腐殖化指数（HIX）小于0.6,r_（T/C）（荧光峰T与荧光峰C荧光强度比值）小于2,表明夏季太湖CDOM内源特性相对强烈.研究显示,除ρ（DOC）外,CDOM与其他水质参数在第一主成分上（贡献率为90.8%）均存在显著相关关系,说明各水质参数的来源存在相似性,并且受生物自生源影响更为显著.      

覆盖金属氧化物对湖泊沉积物溶解性有机质特征的影响

为揭示不同金属氧化物对湖泊沉积物DOM（溶解性有机质）影响机制,通过室内模拟试验,在沉积物表层分别覆盖Fe、Al、Mn氧化物及湖沙后培养1 a,并利用三维荧光和紫外光谱方法进行表征.结果表明:① 覆盖Al、Fe、Mn氧化物和湖沙主要降低了0~3 cm沉积物的w（DOC）,降幅分别为8.61%、6.27%、22.38%和0.44%. ② 沉积物中DOM的类络氨酸峰（peak B₁）和类色氨酸峰（peak T₂）均产生较大变化.其中三种氧化物均显著降低了上层沉积物中DOM的peak T₂,使底层DOM的peakT₂显著增加. Mn氧化物使DOM的peak B₁降低,Fe和Al氧化物使DOM的peak B₁增加,湖沙则使两类峰均降低. ③ 覆盖金属氧化物改变了沉积物DOM结构特征,其中覆盖Fe氧化物增强了其芳香性,而覆盖Mn氧化物和Al氧化却降低其芳香性,但三者均使DOM腐质化程度及官能团数量增加,并使FI（Fluorescence Index,荧光指数）增大,表明DOM向生物源转化.研究显示,沉积物表层覆盖金属氧化物影响了沉积物中DOM迁移和转化,并促进了其降解,导致其分子量和腐殖化程度增加.