提升水库下游河流水质的生态放流量确定和可行性分析

大型水利枢纽工程在防洪、发电、供水、航运等诸多方面发挥巨大作用的同时,也改变了河流的天然水文情势,导致下游河流流量减少,削弱了河流水体的自净能力,威胁河流生态系统功能和物种多样性.在此背景下,选定松辽流域石头口门水库及其下游饮马河为研究对象, 首先分析了饮马河主要污染组分COD和NH₃-N浓度的变化趋势以及前期石头口门水库的生态放流措施对下游河流水环境质量的改善效果,然后基于河流水动力和水质模型,通过目标水质反推水库的生态放流量,从而拟定了一套进一步提升河流水环境质量的水库生态放流方案.最后基于水库均衡分析论证了方案的可行性.研究结果表明,原有的水库生态放流计划实施后,劣V类水体同比减少54.55%,效果较为明显.为了满足“十四五”水质目标,进一步提升河流水质,除10月和12月以外,其它月份的生态放流量均需要提高,年生态补水量增加1425万m³,能够满足水库的供水、灌溉需求和蓄水计划,方案具有可行性,能够有效缓解河流水体污染,提升水质.     

有机质含量及其组分对洱海沉积物磷吸附-释放影响

研究了洱海不同湖区沉积物有机质含量、组分及其吸附-释放磷的特征,试图揭示有机质含量及组分对沉积物磷吸附-释放行为的影响机制.结果表明,洱海沉积物磷释放潜能随着沉积物中有机质(TOM)含量的增加而增大,而沉积物磷的最大释放速率(V释,max)和最大释放量(Q释,max)随沉积物中轻组有机质(LFOM)含量的增加而增大,释放平衡时间随活性有机质(ASOM)含量的增加而缩短,磷释放强度随LFOM占TOM比例的增加而减弱.沉积物磷的最大吸附速率(V吸,max)、最大吸附量(Q吸,max)和吸附效率随沉积物TOM含量的增加而增大,吸附平衡时间随TOM含量的增加而缩短,吸附强度随ASOM含量的增加而增强,吸附-解析平衡浓度(EPC0)随ASOM含量的增加而降低.沉积物磷释放后再吸附过程中磷释放的Q释,max和再吸附的V吸,max随TOM含量的增加而增大,当TOM含量相当时,则随沉积物ASOM含量的增加而降低,再吸附强度随沉积物中LFOM含量的增加而降低.沉积物磷吸附释放容量随有机质总量的增加而增加,吸附释放平衡浓度随有机质活性的增加而降低,释放强度和速率随有机质分解程度的增加而降低,吸附强度和速率随有机质活性的增加而增加.     

欧洲污染物排放与转移登记制度简介

污染物排放与转移登记制度（简称PRTR制度）,是发达国家为了对化学污染物质进行更严格的管理而实行的一种管理制度。该制度起源于1984年,最早实行的是荷兰,其后美国、欧盟、澳大利亚、加拿大、韩国、日本等国家也相继实施了PRTR制度。本文着重介绍了欧盟污染物排放与转移登记制度的发展历史,并就EPER和E—PRTR进行了简单的比较。     

土壤酸沉降缓冲机制的探讨

选取南方主要酸沉降区土壤作模拟酸雨淋溶实验,分析在酸雨作用下各土壤盐基离子的淋溶特性,硅、铝元素的释放规律及淋出液的 pH值变化特点。在此基础上,对土壤酸沉降的缓冲机制进行了探讨。      

Phosphorus speciation and effects of environmental factors on release of phosphorus from sediments obtained from Taihu Lake,Tien Lake,and East Lake

Phosphorus is considered the primary nutrient limiting eutrophication. The release of phosphorus from sediments not only provides hydrophytes with essential nutrients, but can also produce entrophication in lakes. In this study, the sediment characteristics, phosphorus speciation, and environmental factors affecting phosphorus release from sediments from Taihu Lake, Tien Lake, and East Lake were investigated. The results indicated that phosphorus levels of sediments ranged from 647 ± 67 to 2343 ± 122 mg/kg. Inorganic phosphorus comprised the majority of total phosphorus. The main phosphorus speciation of sediments obtained from Taihu Lake and Tien Lake was Residual-P, and the main phosphorus speciation of sediment obtained from East Lake was NaOH-P. Phosphorus release occurred in acidic and alkaline conditions but more frequently under alkaline conditions. The amount of phosphorus released from the sediments increased as the disturbing intensity rose. In addition, less phosphorus was released in natural than anaerobic conditions. The amount of phosphorus released was elevated as temperature increased.     

水葫芦对滇池底泥氮磷营养盐释放的影响

为了探讨水葫芦对富营养湖泊底泥氮磷营养盐释放的影响,通过原位采集滇池柱状底泥,以蒸馏水为上覆水,进行了25d的室内静态模拟实验。实验比较了水葫芦处理组和空白对照组底泥氨氮（NH4-N）、硝态氮（NO3^-N）、溶解性总氮（DTN）、正磷酸盐（PO4^3--P）等的释放特征。结果表明,与对照组相比,水葫芦处理组上覆水溶解氧、pH显著性降低,而PO4^3-P浓度显著性升高;在实验前2d,水葫芦处理组上覆水NH4^＋N和DTN浓度显著性高于对照组,而在5～25d时,其显著性低于对照组。根据上覆水营养盐浓度、水葫芦植株吸收营养盐总量,推算底泥氮磷营养盐释放的平均速率,表明水葫芦加速了滇池底泥氮、磷营养盐的释放速率,处理组氮、磷释放速率分别为对照组的5．3～170．2和1．5～21．6倍。     

Preparation of controlled nano-MgO and investigation of its bactericidal properties

Nano-MgO is a good bactericide but with strong alkalinity in water due to its rapid hydrolysis. To control its hydrolysis rate and keep its bactericidal properties, we synthesized nano-MgO microspheres using chitosan-alginate system in this study. The synthesized nano-MgO release-controlled microspheres (nMgO-RCM) were with 0.98-1.20 mm of particle sizes. Also, their embedding ratio and loading percentage was 63.52% and 12.27%, respectively. Based on the characterization results, nano-MgO was only observed on surface of the nMgO-RCM. Its release rate from the nMgO-RCM could be controlled by the chitosan-alginate system, and the observed rate constant (k_obs) increased from 0.0289 h⁻¹ to 0.0358 h⁻¹ with the increment of the dosage from 10 mg L⁻¹ to 80 mg L⁻¹. Furthermore, the nMgO-RCM could maintain pH value lower than 8.5 and colony counts less than 20 CFU mL⁻¹ for at least 120 h.     

不同曝气方式对城市重污染河道水体氮素迁移与转化的影响

以南京仙林大学城的重污染河道水体为对象,利用模拟方法研究不同曝气方式（底泥曝气、水曝气）对水体氮素迁移与转化的影响.结果表明,在缺氧和温度升高条件下,底泥氮素主要以NH 4＋-N形式向上覆水释放;上覆水NH 4＋-N的最大累积量表现为：水曝气〈底泥曝气〈对照,3种工况下上覆水中NH 4＋-N的最高质量浓度分别为9.40...     

小兴凯湖表层底泥磷吸附容量及潜在释放风险

利用沉积物磷吸附指数(PSI)和磷吸附饱和度(DPS)研究了小兴凯湖表层沉积物的磷吸附容量,分析了沉积物中磷的吸附饱和度(DPS)与其他指标的相关关系,并讨论了不同采样点湖泊沉积物中磷的潜在释放风险.结果表明:13个采样点的表层沉积物的PSI为9.78~197.53(mg?L)/(100g?μmol),平均值为59.77(mg?L)/(100g?μmol);DPS为9.95%~24.47%,平均值为15.41%.PSI与草酸铵提取的磷(Pox)极显著正相关,与草酸铵提取的铁、铝(Feox,Alox)显著正相关,草酸铵提取的铁是影响PSI的主导因素;DPS主要受沉积物中原有吸附态磷的影响.此外,磷释放风险指数(ERI)8.99%~129.94%的计算结果表明:小兴凯湖表层沉积物中磷释放诱发富营养化的风险处于高度风险范围,其中,受农业面源污染影响较大的北岸区域相比其他区域发生富营养化的风险更高.     

Release Characteristics of Nutrients from Polymer-coated Compound Controlled Release Fertilizers

Reliable information regarding release characteristics of nutrients from a polymer-coated controlled release fertilizer (CRF) is essential for beneficial agronomic and environmental results. Significant knowledge regarding nitrogen release from polymer-coated urea was gained while the information regarding the release of the different nutrients contained in polymer-coated compound N–P–K CRF remains limited. An experiment in which major factors affecting the differential release of nutrients from two coated compound CRF was performed in free water, water saturated sand and sand at field capacity. In general, nitrate release was the fastest, followed by ammonium and potassium whereas phosphate was significantly slower, with a rate of linear release in free water 45–70% slower than that of nitrate. Little differences were obtained for the lag periods of nitrate, ammonium and potassium release (2–10 days) under the experimental conditions, whereas for P they were one order of magnitude larger. The main factor slowing the release was assumed to be the lower solubility of ions with P being the least soluble. Release into free water was, expectedly, somewhat faster than that into saturated sand and significantly faster as compared to sand at field capacity and particularly so for P. Raising the temperature from 20 °C to 40 °C increased the rate of linear release of the different nutrients. The energy of activation, EA_rel, estimated for the linear release, of the different nutrients, was narrow ranging between 37 to 46 (KJ mol⁻¹) whereas the mean values obtained for the two CRF, differing by 50% in coating thickness, was non-significant. However, EA_rel was significantly different in different media. The complex effect of temperature on the lag period and nutrient interactions during release deserve further investigation.