Fetal death secondary to needle laceration during 2nd trimester aminiocentesis: A case report

A case of fetal death secondary to a needle laceration during a second trimester amniocentesis is presented. The need for careful pathologic evaluation of fetuses lost subsequent to these procedures is stressed.     

水污染造成的环境经济损失分析

立足于我国水资源现状，对造成水污染损失的主要影响因素进行分析。探讨适合于我国国情的水污染损失的计算方法。以南方某市为例，计算该市水污染损失，得到了一些有益的结论．给政府部门提供了一个较为准确的损失数据。通过政府的干预或经济法律手段，加大水资源保护管理工作的力度。     

全国土壤侵蚀量估算及其在吸附态氮磷流失量匡算中的应用

应用土壤流失方程(USLE),根据我国土壤水力侵蚀分类分级标准,建立了大尺度区域土壤侵蚀量的估算模型;基于GIS技术平台,利用土壤普查数据,构建了全国表层土壤氮磷含量数据库,完成了2000年全国境内水土流失影响下吸附态氮磷的流失量估算.经数据合理性分析验证后得出以下结论:(1)全国因水土流失引发的吸附态氮素和磷素的流失总量分别达到104.22×104t和34.65×104t;(2)长江、珠江和黄河三大流域的吸附态氮、磷流失量之和分别占全国总量的83%和89%,单位面积(1km2)吸附态氮、磷的流失量分别介于6.0×10-4～0.53t和2.1×10-4～0.13t之间;(3)吸附态氮的重点流失区主要分布在长江中上游水土易蚀区、黄河中游沟壑区、西辽河上游区、珠江流域红水河、西江等上游区以及怒江、澜沧江下游区.     

长江河口硅和磷生源要素质量浓度的变化特征

根据近年来长江河口区域内大通水文站的记录和近期在长江入海河口区上海段多个采样点的生源要素质量浓度实测数据,比较水中可溶性硅酸盐和磷酸盐的质量浓度,分析在长江入海河口区水中硅和磷元素含量的主要变化特征.结果表明,长江水中的硅酸盐和磷酸盐从长江入海河口进入大海的过程中,其质量浓度有降低的趋势,它们在长江入海河口的多年的质量浓度变化趋势是相反的.长江入海河口区域上游的磷酸盐质量浓度升高幅度较大,而硅酸盐变化不大,硅酸盐、磷酸盐质量浓度在长江河口区进入海洋的过程中迅速降低.      

水环境退化经济损失的计量方法及其应用

水环境退化较难以市场价格方式体现,是绿色GDP核算的一大难点.分析了影响水环境退化的社会经济因素、自然因素,在此基础上,构建了水环境退化的计量模型,并将社会经济发展的阶段性特征、水资源供需矛盾、降水补给变异特征和水质状况纳入模型中,采用不同参数进行描述,以保证模型的逻辑完备性和计算的简洁性.在湖州市绿色GDP核算过程中,采用该模型分别计算各县区2001-2004年水环境退化的经济损失.这些损失与当地水资源供需矛盾、水污染状况、社会经济发展等因素变化状况相符,准确反映了湖州市水环境退化的实际状况.结果表明,水环境退化的经济损失,除水污染程度外,还受到社会经济因素和降水补给等自然因素的影响.      

N和P对锥状斯氏藻(Scrippsiellat trochoidea)生长及孢囊形成的影响

在实验室设置了5个N、P浓度梯度,研究了它们对锥状斯氏藻（Scrippsiella trochoidea）营养细胞生长和孢囊形成的综合效应。结果表明,当N、P浓度分别超过10和1．5μg／L时,就能维持锥状斯氏藻一定的种群数量,而在高N、P浓度组（N浓度为500μg／L,P浓度为74μg／L组）的生长势态明显优于其他浓度组,稳定生长期持续时间较长,且有着较高的细胞比生长速率。孢囊一般在营养细胞达到稳定生长期后开始形成,但低营养盐浓度组孢囊开始形成的时间较早。各试验组孢囊形成率相近,最终形成率为17．8％～35．6％。     

Effect of humic substances on the precipitation of calcium phosphate

For phosphorus （P） recovery from wastewater, the effect of humic substances （HS） on the precipitation of calcium phosphate was studied. Batch experiments of calcium phosphate precipitation were undertaken with synthetic water that contained 20 mg/L phosphate （as P） and 20 mg/L HS （as dissolved organic carbon, DOC） at a constant pH value in the range of 8.0-10.0. The concentration variations of phosphate, calcium （Ca） and HS were measured in the precipitation process; the crystalline state and compositions of the precipitates were analysed by powder X-ray diffraction （XRD） and chemical methods, respectively. It showed that at solution pH 8.0, the precipitation rate and removal efficiency of phosphate were greatly reduced by HS, but at solution pH ≥9.0, the effect of HS was very small. The Ca consumption for the precipitation of phosphate increased when HS was added; HS was also removed from solution with the precipitation of calcium phosphate. At solution pH 8.0 and HS concentrations ≤3.5 mg/L, and at pH ≥ 9.0 and HS concentrations ≤ 10 mg/L, the final precipitates were proved to be hydroxyapatite （HAP） by XRD. The increases of solution pH value and initial Ca/P ratio helped reduce the influence of HS on the precipitation of phosphate.     

关于气溶胶颗粒物沉积率系数平均方法模型的改进研究

气溶胶颗粒物在壁面的沉积率系数模型的研究已经成为现代气溶胶动力学研究的重要课题.本文通过实验腔测量和理论分析相结合,对Koivisto等(2012)提出的平均方法模型(AM)中的关键参数(即时间间隔)的选取和对测量数据量的要求两个问题进行研究.选取目前广泛使用的最小二乘法模型(LSM)和Lai和Nazaroff(2000)提出的理论分析模型进行对比.研究发现,AM模型中的时间间隔这一关键参数,应由目前的50矫正为20;AM模型和LSM模型均要求实验测量数据个数等于或者大于10,但是AM模型在小数据量情况下的预测结果更精确.     

紫色土旱坡地油菜/玉米轮作下氮流失的年际变化特征

明确三峡库区紫色土旱坡地氮流失的年际变化特征,为库区的施肥管理措施和面源污染治理提供参考.依托中国科学院成都山地灾害与环境研究所三峡库区试验站,于2018～2020年连续3 a设置不施肥(CK)、常规施肥(F)、优化施肥(OF)、化肥减量配施生物炭(BF)和化肥减量配施秸秆覆盖(SF)5种处理,研究紫色土旱坡地在油菜-玉米轮作模式下氮流失的年际变化特征.结果表明：(1)三峡库区紫色土旱坡地地表径流主要发生在5月和8月,壤中流主要发生在6～10月. 2018～2020年降雨量逐年增加,各处理地表径流产流量逐年减少,壤中流产流量大致呈逐年增加的趋势,年尺度下,壤中流产流量和产流次数均高于地表径流.(2)2018～2020年每年各形态氮的最高流失浓度出现时间大概一致,地表径流全氮、铵态氮和硝态氮最高流失浓度分别出现在5、 8～10和7月,壤中流各形态氮最高流失浓度分别出现在10、 10和5～7月.(3)地表径流各形态氮流失通量呈逐年降低趋势,壤中流各形态氮流失通量大致逐年增加.(4)生物炭和秸秆还田第一年降低氮流失通量的效果较好,但后续两年还田反而加剧了氮素流失通量.因此,三峡库区紫色土旱坡...     

Effect of low-molecular weight organic acids on phosphorus release and phytoavailabilty of phosphorus in phosphate rocks added to soils

Phosphorus (P) is critically needed to improve soil fertility in many parts of the world. The use of water-soluble P fertilizers, e.g., single super-phosphate and triple super-phosphate in developing countries to improve crop production has been limited primarily by their high cost. The presence of indigenous phosphate deposits in some countries provides an incentive for direct application or local chemical treatment at low cost to improve the solubility of low reactive phosphate rocks (PRs). The use of naturally occurring low-molecular weight organic acids (LMWOAs) that are produced in soil as microbial metabolites or plant exudates from dead or living cells represents a new perspective in PR research. The LMWOAs contain various functional groups that may play a significant role in PR dissolution. Little information is available, however, about the potential of LMWOAs in releasing P from PRs. This study reports P release from 12 PRs, four each of low, medium, and high reactivity, obtained from various deposits (Kodjari, Tahoua, North Carolina, Gafsa, Khouribga, Tilemsi Valley, Central Florida, Sechura, Minjingu, North Florida, Hahotoe, and Parc W) using nine LMWOAs containing mono-, di-, and tri-carboxylic groups and a mineral acid (H₂SO₄). Laboratory studies showed that the organic acids are effective in releasing P from low and medium reactive PRs, but very ineffective in releasing P from high reactive PRs. The average amounts of P released by all the organic acids from the three types of PRs were 65.5 mmol kg⁻¹ PR from the low reactive PRs, 55.1 mmol kg⁻¹ from the medium, and 11.1 mmol kg⁻¹ from the high; those released from across all the PRs were 21.9 by the mono-carboxylic acid group, 54.2 by the di-carboxylic acid group, and 57.0 mmol P kg⁻¹ by the tri-carboxylic acid group. The P released was negatively correlated with the equilibrium pH, but positively correlated with Ca released from the PRs. Laboratory incubation studies on the release of P from PRs added to soils with or without organic acids and incubated at 25 °C for 15, 30, and 45 days showed that the percentage of plant-available P released varied considerably from 0.95 in the Kodjari PR to 40.1% in the North Carolina PR and was related to PR reactivity. A greenhouse study with corn (Zea mays L.) grown for 60 days on soils treated with PRs or with PRs mixed with organic acids showed that corn response to addition of oxalic or citric acid varied with P rates and PR sources, suggesting that organic acids have potential as amendments for increasing plant-available P in PR-treated soils.