永定河沉积物中磷的存在形态及其指示意义

采集官厅水库的永定河入库口附近沉积物,采集深度77cm,以1cm做为一个层位单元进行分割,测定其中11个层位的总磷,同时对这些层位沉积物中二钙结合态磷、八钙结合态磷、铝结合态磷、铁结合态磷进行连续分级提取,有机磷通过灼烧法测定,残留态磷由总磷与上述五种形态磷差减确定。结果显示:沉积物中总磷含量在580.3~1276.2μg/g,主要成分为无机磷,平均占总磷的比例为88%;残留态磷为沉积物中磷的主要形态,含量占总磷50%以上。在沉积物深度75~20cm的沉积年份中,永定河向官厅水库输送的残留态磷量不断增加,且增速逐渐加快,主要为水土侵蚀的产物。从沉积深度20cm以来的沉积年份里,总磷的输入量不断减少,但以二钙结合态磷为主的生物有效磷输入量随总磷的含量降低而持续增加,主要来自工业和生活污水,反映了官厅水库上游永定河流域内工业和生活污水排放所占的比重日益增加,成为官厅水库富营养化污染的主要来源,以致官厅水库富营养化的趋势增强。     

Tracing suspended sediment and particulate phosphorus sources in catchments

Information on suspended sediment and particulate P (PP) sources is an important requirement in many catchment-based diffuse source pollution studies, in order to assist with model validation and to provide information to support the development of effective sediment and phosphorus control strategies. Such information is, however, frequently unavailable or difficult to assemble. In the study reported, source fingerprinting procedures were successfully used to assemble this information for seven sub-catchments in the Hampshire Avon catchment and five sub-catchments in the Middle Herefordshire Wye catchment. The results provide important new information on the relative importance of the contributions from surface and channel/subsurface sources to the suspended sediment and PP fluxes from the catchments. In the Wye sub-catchments channel/subsurface sources contributed 40–55% of the overall suspended sediment flux and 21–43% of the PP flux from the catchments. Equivalent values for the Avon were 1–41% and 1–54%, respectively. Combination of the information on the relative importance of surface and channel/subsurface sources with measured suspended sediment fluxes has provided the first estimates of the specific fluxes of sediment and PP attributable to channel/subsurface sources for UK catchments. The former are as high as 15–20 t km⁻² year⁻¹ in some of the Wye sub-catchments, whereas the latter exceeded 0.1 kgP ha⁻¹ year⁻¹ in the same sub-catchments. The results emphasize the need to take account of potential contributions from channel/subsurface sources when using measured suspended sediment and PP flux data to validate predictions derived from models incorporating only surface contributions.     

Alkaline Phosphatase Activity and Utilization of Dissolved Organic Phosphorus by Algae in Subtropical Coastal Waters

Alkaline phosphatase activity (APA) and the availability of dissolved organic phosphorus (DOP) to marine algae were determined in Xiamen Bay and in algal batch culture systems. Results showed that APA changed with seasons, increasing to the highest value in summer and decreasing to the lowest in autumn and spring in Xiamen Bay. Tests on natural populations of planktonic algae and bacteria community showed that algae were mostly responsible for DOP utilization, while bacteria could not take up DOP compounds. Results from algal batch cultures also supported the above conclusion. Relationships between APA and environmental factors indicated that APA was negatively correlated with phosphorus level such as phosphate and small molecular DOP, and APA played an important role in utilization of DOP by algae. All the results emphasized the ecological significance of DOP in subtropical coastal waters.     

Influence of land use on the persistence effect of riverine phosphorus

The persistence effect contribution of legacy nutrients is often cited as a reason for little or no improvement in water quality following extensive implementation of watershed nutrient mitigation actions, yet there is limited knowledge concerning factors influencing this response, often called the “persistence effect.” Here, we adopted detrended fluctuation analysis and Spearman analysis methods to assess the influence of land use on the watershed phosphorus (P) persistence effect, using monthly water quality records during 2010–2016 in 13 catchments within a drinking water reservoir watershed in eastern China. Detrended fluctuation analysis was used to calculate the Hurst exponent α to assess watershed legacy P characteristics (α  ≈ 0.5, α  > 0.5, and α  < 0.5 indicate white noise, persistence, and anti‐persistence, respectively). Results showed weak to strong P persistence (0.60–0.81) in the time series of riverine P in the 13 catchments. The Hurst exponent α had negative relationships with agricultural land (R = ?.47, p = .11) and developed land (R = ?.67, p = .01) and a positive relationship with forest land cover (R = .48, p = .10). The persistence effect of riverine P was mainly determined by retention ability (biogeochemical legacy) and migration efficiency (hydrological legacy). A catchment with strong retention capacity (e.g., biomass uptake/storage and soil PO₄ sorption) and low migration efficiency results in a stronger persistence effect for riverine P. In practice, source control is more effective in catchments with weak persistence, whereas sink control (e.g., riparian buffers and wetlands) is preferred in catchments with strong persistence effects.     

淡水磷酸盐氧同位素前处理方法的优化

磷是地表水体中的关键性营养盐,在水生生态系统的物质循环与能量流动方面发挥着重要作用,研究水体中磷的来源、转化与归趋对于了解水环境的演变过程与科学保护具有重要意义.近年来,磷酸盐氧同位素(δ18 O P)技术已逐渐应用于淡水环境中磷的来源示踪与生物地球化学循环研究,其样品前处理主要沿用海水方法体系.相比而言,淡水样品中PO 3-4浓度通常较低,有机质和干扰离子含量却较高,复杂的样品前处理过程极大地制约了δ18 O P分析在淡水环境体系的广泛应用.为此,本研究针对现有海水样品δ18 O P前处理方法在地表淡水环境的适用性加以检验,并进行了三点优化改进:①将MAGIC沉淀步骤使用的MgCl 2替换为Mg(NO 3)2,避免了Cl-的干扰,减少AgCl杂质的生成;②调节生成Ag3PO4溶液pH值为8.0,保证Ag3PO4沉淀快速完全;③对Ag3PO4沉淀过程采用避光处理,降低了AgNO 3及Ag3PO4可能的光解影响,提高了Ag3PO4的纯度,使δ18 O P的测试结果更为准确.本改进方法为后续利用δ18 O P技术深入探究淡水环境中磷的生物地球化学循环与生态环境效应提供了有益的方法借鉴.     

What controls levels of dissolved phosphate and ammonium in surface waters?

Dissolved inorganic nutrient pools are small relative to particulate pools, and dissolved pools turnover rapidly. It has been observed that pools change little from day to day on the sampling scales usually employed. A simple model is presented where uptake and regeneration rates balance to cause a local steady state concentration for dissolved inorganic nutrients. Enrichment and dilution perturbation experiments with lake water support the idea of steady state nutrient concentrations. Although inorganic nutrient concentrations are often controlled by biota, the absolute concentrations present tell little about the activity of that biota.     

1988-2018年滇池氮磷比的时空演变特征与原因解析

氮、磷浓度是制约湖泊营养状态和生产力水平的重要环境因子,而氮磷化学计量比是湖泊生态系统的主要指标,因此,判识氮磷比变化趋势及其驱动力对湖泊生态恢复具有重要意义.研究基于19882018年连续观测数据,分析了滇池氮磷浓度和氮磷摩尔比(简称氮磷比)的时空分布演变特征;采用多元线性回归模型分别对滇池草海和外海氮磷比驱动效应进行定量解析,筛选出影响湖体氮磷比变化的潜在驱动因子.结果表明:①19882018年滇池氮磷比呈现显著的线性上升趋势,其中草海和外海氮磷比分别上升1.3和0.7 a^-1.②草海和外海分别在2008年和2004年发生了氮磷比上升突变,突变前上升归因于总氮浓度快速增加,突变后则是由于总磷浓度下降较快.③滇池的氮磷浓度变化主要是受流域氮磷输入负荷、跨流域调水、流域氮磷削减、风速和水位的综合影响,但受控因子在不同区域可能存在差异.④气温是滇池氮磷比变化的主要驱动因子,流域人为氮磷输入差异是滇池氮磷比变化的次要驱动因子.     

磷灰石结晶法降低天然水体中磷浓度Ⅰ.不同反应物对降磷效果的影响

利用矿物磷灰石低溶度积特征,以晶体磷灰石作晶胞,引入氟、钙等离子,诱使水中溶解性磷酸盐在磷灰石晶体上沉淀、结晶,使水溶液中磷浓度明显降低。探讨了钙、磷灰石、氟、氯的加入对降磷效果的影响,初步分析了生成产物的结构。实验溶液中磷初始浓度约为5 mg/L,经磷灰石结晶后,最低可降至10μg/L以下,除磷效率可达99%以上。     

青海湖地区生物中正构烷烃及其氢同位素组成与影响因素

青海湖是我国最大的内陆咸水湖泊。本文应用GC-MS和GC-TC-IRMS同位素分析技术,对青海湖水生生物和周围地区陆生生物中正构烷烃及其氢同位素进行了分析,研究了生物中正构烷烃及其同位素组成。结果显示了不同生物中正构烷烃碳数分布范围在C1 5~C33之间,呈单峰型分布;主峰碳数是水生生物(除海韭菜外)相对较低,主要为C23和C25,陆生木本植物次之,为C27;陆生草本植物较高,为C27和C29;CPI值分布在4.0~29.7之间;ACL值为26.0~29.6,分布与植物类型有关。青海湖水生生物中正构烷烃氢同位素组成分布在-209.8‰~-85.6‰之间,平均值为-169.2‰~-121.2‰;陆生植物的正构烷烃δD值为-196.7‰~-84.3‰之间,平均值为-173.0‰~-108.6‰。青海湖不同水生生物和不同陆生生物之间的正构烷烃氢同位素组成差别显著。研究发现,湖泊的含盐量对水生植物的正构烷烃氢同位素具有显著影响,环境湿度和降水量明显影响了陆生植物的正构烷烃氢同位素组成;植物的正构烷烃平均氢同位素组成随着其ACL值增加,具有变轻的趋势;不同种类植物的正构烷烃合成期间具有不同的氢同位素分馏效应,与陆生植物相比较,水生植物的正构烷烃相对于环境水更富集轻氢同位素,并且随着ACL值增加,环境水和正构烷烃之间的氢同位素分馏增大。     

华北平原高氟地下水中稀土元素分布和分异特征

高氟地下水是世界各国研究者广泛关注的重大环境问题。尽管对高氟地下水的化学特征、形成机理和扩散机制等已有不少研究,但其稀土元素(REE)的含量和分异特征以及这些特征能否反映高氟地下水的形成和分布尚不清楚,这在一定程度上限制了REE在高氟地下水中的运用。本研究以地下水氟离子异常严重地区——华北平原为研究区,沿地下水流向采集浅层和深层地下水样,研究分析了水中氟离子和REE的地球化学特征。浓度分析结果表明地下水氟离子浓度介于0.28 mg/L和9.33 mg/L之间,其中55%超出我国饮用水标准规定值1.0 mg/L;PHREEQC计算结果反映地下水中氟以NaF、CaF⁺、MgF⁺和自由态F^-形式存在,其中自由态F^-含量占主导(85.42%99.39%);高氟地下水主要分布于中部冲积湖积平原以及东部冲积海积平原,60%高氟地下水样分布在180 m深度以下;水化学图件分析结果指示浅层高氟地下水的形成主要受蒸发浓缩作用的控制,而深层高氟地下水是水岩相互作用下的矿物溶解和离子竞争吸附共同作用的结果。研究区地下水REE含量处于pmol/L至nmol/L级别,PHREEQC模拟计算结果表明REE主要以碳酸络合物( {\mathrm{REECO}}_3^{+}和$REE(CO_{3})_{2}^{-})$的形式存在,与氟离子络合的稀土元素(REEF²⁺和 {\mathrm{REEF}}_2^{+})占01.18%;上陆壳(UCC)标准化结果显示,所有地下水均呈重REE(HREE)和中REE(MREE)相对于轻REE(LREE)富集的模式,且具有显著Ce负异常(0.11* = Ce_UCC/(La_UCC×Pr_UCC)^0.5<2.29)特性;地下水富HREE主要归因于HREE比LREE优先与碳酸根络合,并且形成更加稳定的碳酸络合物。沿地下水流向,深层地下水中总REE含量与地下水中氟浓度均呈现不断上升的变化趋势,同时高氟地下水比低氟地下水更易富集重稀土元素,说明稀土元素对深层含水层富氟行为具有一定的指示作用。