赤潮灾害经济损失评估技术方法

为有效应对赤潮灾害防灾减灾、灾后救援及管理的需求,在综合分析前人提出的赤潮灾害损失评估技术方法的基础上,参考赤潮灾害对受灾体的危害特点,结合实际工作的需求及在实际中可获取的业务数据,提出了赤潮灾害经济损失评估指标体系;根据灾害经济学理论,借鉴其他自然灾害经济损失评估的先进思想,采用市场价格法,分别建立了包括海水养殖业经济损失、滨海旅游业经济损失、赤潮灾害业务与应急监测费用和赤潮灾害处置费用的赤潮灾害经济损失评估模型;最后,提出了赤潮灾害损失评估的技术流程。     

陕南秦巴山区地质灾害发育及空间分布规律

为进一步研究陕南秦巴山区地质灾害发育及空间分布规律,对区内地质灾害的数量、规模、物质组成等进行概率统计分析,结果显示:该区地质灾害以堆积层滑坡为主,岩质崩塌次之;滑坡规模以小型、浅层和等长式为主,崩塌以小型、等长式为主。地质灾害空间点密度呈"四高两低"分布,崩塌呈"三高四低"分布,泥石流呈"三高两低"分布。地质灾害、断裂、河流及道路的空间分布具有分形特征。滑坡(崩塌)面积与体积(长、宽)之间具有幂律相依性,面积与体积符合对数正态分布。结论为陕南秦巴山区移民搬迁安置选址提供技术支持。     

四环素类抗生素和铜复合污染对猪粪厌氧消化的影响

兽用抗生素和矿物元素添加剂可起到预防动物疾病、促进动物生长、提高饲料转化率等作用,因此被广泛应用于畜禽养殖业。本研究以猪粪中温厌氧消化为研究目标,采用全自动甲烷潜势测试系统,考察了一定浓度的四环素(TC:30 mg·kg~(-1)dry weight,DW)、土霉素(OTC:50 mg·kg~(-1)DW)和金霉素(CTC:15 mg·kg~(-1)DW)对厌氧累积产甲烷量和日产甲烷速率的影响。结果表明,TC、OTC和CTC对猪粪中温厌氧消化累积产甲烷量和日产甲烷速率均有促进作用(累积产甲烷总量提高比例分别为7.9%、0.4%和5.4%)。另外,采用超高效液相色谱-四极杆串联质谱对猪粪厌氧消化前后样品中四环素类抗生素及其代谢产物进行了分析。结果表明,液相中的四环素类抗生素在猪粪厌氧消化过程中得到了明显的去除,去除率达到90%~100%;而固相中只有金霉素和差向异构金霉素有明显的去除效果,去除率分别为41.69%和41.58%。采用Tessier连续提取法对猪粪厌氧消化前后样品中5种形态的铜包括可交换态、碳酸盐结合态、铁锰氧化结合态、有机物结合态、残渣态进行了分析,结果表明,猪粪厌氧消化后,可交换态、碳酸盐结合态和铁锰结合态的铜浓度比厌氧消化前分别降低了1%~9%、0.1%~3%、12%~19%,而有机态和残渣态的铜浓度却在厌氧消化后分别增加了15%~35%、1%~2%。厌氧消化后,70%~80%的铜都是以有机铜的形态存在。铜逐渐从不稳定态转化为相对稳定的有机态和残渣态铜,因此,厌氧消化过程使铜从可生物利用态转变为不可生物利用态,趋于稳定化。     

预测沉积物-水微宇宙系统中化学品浓度变化的多介质模型

沉积物-水微宇宙系统是经济合作发展组织(Organisation for Economic Co-Operation and Development,OECD)颁布的化学品测试准则中推荐的试验系统之一,可用来测试化学品对底栖生物的慢性毒性。为了在试验前对化学品的浓度变化进行预测,进而确定试验方法,以摇蚊慢性毒性试验系统为例,采用环境多介质模型的建模方法,构建了一种可通过化学品理化性质和试验系统参数,对化学品在沉积物-水试验系统中浓度变化进行预测的模型。结合试验数据和文献资料,给出了模型中试验系统参数的推荐取值,并使用Matlab软件中的Simulink工具对模型进行编程和求解。以此模型为基础,给出了模型在3个方面的应用,即预测蓄积时间、预测平衡时间以及拟合试验数据。对80种已有或假想化学品的蓄积时间和平衡时间进行了计算,得出的范围分别为1~204 d和1~73 d。此外,适当修改模型结构和模型参数,也可将其应用于其他暴露场景中。但使用模型对化学品浓度进行预测时发现,模型仅对沉积物中化学品浓度的预测结果较为准确,而对水中化学品浓度的预测结果与实测值相差1~2个数量级。模型对浓度的预测精度未来仍需进一步提高。上述研究结果完善了沉积物-水微宇宙系统试验方法。     

应用概率物种敏感度分布法研究太湖重金属水生生物水质基准

目前广泛使用的水质基准推导方法—物种敏感度分布法存在曲线拟合模型不确定、曲线拟合效果不佳、种内差异欠考虑、基准值不准确等诸多问题,概率物种敏感度分布法可有效解决上述问题。应用概率物种敏感度分布法构建了太湖水体中5种重金属Ag、Pb、Cd、Hg和Zn的概率物种敏感度分布曲线,在此基础上得到了保护水生生物的急性水质基准分别为1.079μg·L~(-1)、637.973μg·L~(-1)、19.465μg·L~(-1)、8.729μg·L~(-1)和105.506μg·L~(-1),慢性水质基准分别为0.108μg·L~(-1)、63.797μg·L~(-1)、1.947μg·L~(-1)、2.340μg·L~(-1)和52.753μg·L~(-1);不同类群间生物对重金属的敏感度存在差异,不同重金属对同一类群生物的毒性也存在差异;通过与国内外已有的重金属水质基准值比较,发现水质基准具有明显的区域性,目前基于国外水质基准或我国整体水域特点来制定的太湖水质标准,往往造成对太湖水生生物欠保护或过保护的状况。     

绿洲边缘新月形沙丘表层沉积物粒度与重金属分布特征

本文以乌兰布和沙漠绿洲边缘工业化城市乌海市下风向典型新月形沙丘为研究对象,分析了新月形沙丘各部位0~10 cm沙物质、沙丘前50 m处大气降尘的粒度及重金属元素变化特征,探讨了重金属物质的来源及其与粒径的相关性,评价了重金属的潜在生态风险.结果表明:沙丘各部位沉积物粒度均以细砂为主,较对照沙丘极细砂含量增高而中砂含量减少.而降尘主要以极细砂、粉粒为主,降尘在沙丘表面的沉降堆积使沙丘表层沙物质细化.沙丘与降尘的重金属含量均为FeMnCrZnCu;Mn、Cu、Zn、Cr含量均高于背景值且发生富集.Mn、Zn含量在空间分布上呈中等变异;Fe、Cu含量在空间分布上为高度变异.Mn、Zn、Cu含量与细颗粒含量呈显著正相关,Zn、Cu含量与中砂含量呈负相关,Fe含量与细砂和中砂含量均呈负相关.Cu、Zn、Cr为人为污染因子,Mn、Fe为自然源因子,但Cr、Mn、Fe又受到自然地质背景和人类活动的共同控制.乌海市下风向新月形沙丘属于低生态风险状态,为轻度污染,需加强废气的治理控制以防重金属污染的进一步加深.     

基于ERA-Interim资料分析青藏高原“湿池”变化特征

论文利用ERA-Interim(0.5°×0.5°,简称ERA)、NCEP/NCAR2(2.5°×2.5°,简称NCEP2)两种不同分辨率的再分析资料和探空观测资料,首先分析了夏季(7月)和冬季(1月)青藏高原(以下简称高原)上大气水汽含量大值区(简称"湿池")的区域分布特征,然后基于ERA资料分析了1979—2012年间高原"湿池"的一些变化特征,发现了一些新的事实。主要结果包括:在对流层中上层,高原上无论夏、冬季都有大气水汽含量的高值中心——高原"湿池"存在。夏季7月高原"湿池"强度最强,ERA资料除了在高原南部有自西到东的连续高湿中心带外,在高原西北部还有一个高湿中心;NCEP2资料仅在高原东南部和西南部有两个高湿中心。冬季1月,两种资料均只在高原东南部有高湿中心。总体上,ERA资料与探空观测资料的高湿中心区更为接近。7月,高原南部高湿中心在1990年代中期(1994—1996年)之后持续偏强,西北部中心强度有弱—强—弱—强交替变化特征;1月,高湿中心在1980年代末期开始持续偏强。高原南部高湿中心带在7月几乎是一个连续的区域,1996年以后这一特征更为明显,在1月则是分为东西两段的高湿中心带。     

Impact of dissolved organic matter on the photolysis of the ionizable antibiotic norfloxacin

Norfloxacin (NOR), an ionizable antibiotic frequently used in the aquaculture industry, has aroused public concern due to its persistence, bacterial resistance, and environmental ubiquity. Therefore, we investigated the photolysis of different species of NOR and the impact of a ubiquitous component of natural water — dissolved organic matter (DOM), which has a special photochemical activity and normally acts as a sensitizer or inhibiter in the photolysis of diverse organics; furthermore, scavenging experiments combined with electron paramagnetic resonance (EPR) were performed to evaluate the transformation of NOR in water. The results demonstated that NOR underwent direct photolysis and self-sensitized photolysis via hydroxyl radical (·OH) and singlet oxygen (¹O₂) based on the scavenging experiments. In addition, DOM was found to influence the photolysis of different NOR species, and its impact was related to the concentration of DOM and type of NOR species. Photolysis of cationic NOR was photosensitized by DOM at low concentration, while zwitterionic and anionic NOR were photoinhibited by DOM, where quenching of UOH predominated according to EPR experiments, accompanied by possible participation of excited triplet-state NOR and ¹O₂. Photo-intermediate identification of different NOR species in solutions with/without DOM indicated that NOR underwent different photodegradation pathways including dechlorination, cleavage of the piperazine side chain and photooxidation, and DOM had little impact on the distribution but influenced the concentration evolution of photolysis intermediates. The results implied that for accurate ecological risk assessment of emerging ionizable pollutants, the impact of DOM on the environmental photochemical behavior of all dissociated species should not be ignored.     

Rapid and simple spectrophotometric determination of persulfate in water by microwave assisted decolorization of Methylene Blue

A rapid and simple method for determination of persulfate in aqueous solution was developed. The method is based on the rapid reaction of persulfate with Methylene Blue(MB) via domestic microwave activation, which can promote the activation of persulfate and decolorize MB quickly. The depletion of MB at 644 nm(the maximum absorption wavelength of MB) is in proportion to the increasing concentration of persulfate in aqueous solution. Linear calibration curve was obtained in the range 0–1.5 mmol/L, with a limit of detection of 0.0028 mmol/L. The reaction time is rapid(within 60 sec), which is much shorter than that used for conventional methods. Compared with existing analytical methods, it need not any additives, especially colorful Fe2+, and need not any pretreatment for samples, such as p H adjustment.     

Effect of six kinds of scale inhibitors on calcium carbonate precipitation in high salinity wastewater at high temperatures

Precipitation of calcium carbonate(Ca CO3) scale on heat transfer surfaces is a serious and expensive problem widely occurring in numerous industrial processes. In this study, we compared the scale inhibition effect of six kinds of commercial scale inhibitors and screened out the best one(scale inhibitor SQ-1211) to investigate its scale inhibition performance in highly saline conditions at high temperature through static scale inhibition tests. The influences of scale inhibitor dosage, temperature, heating time and p H on the inhibition efficiency of the optimal scale inhibitor were investigated. The morphologies and crystal structures of the precipitates were characterized by Scanning Electron Microscopy and X-ray Diffraction analysis. Results showed that the scale inhibition efficiency of the optimal scale inhibitor decreased with the increase of the reaction temperature. When the concentration of Ca2+was 1600 mg/L, the scale inhibition rate could reach 90.7% at 80°C at p H 8. The optimal scale inhibitor could effectively retard scaling at high temperature. In the presence of the optimal scale inhibitor, the main crystal structure of Ca CO3 changed from calcite to aragonite.