总量控制费用分摊的多目标规划模型及解法

文章指出了污染物总量控制规划中公平合理分摊优化治理投资费用的重要性，分析了现有的优化治理投资费用分摊方法存在的问题，建立了公平合理分摊优化治理投资费用的多目标规划模型，提出用最短距离理想点法加以求解，并通过实例验证了该方法的合理性。结果表明该模型及解法既可以保证总量控制规划方案的社会整体效益最大，又不失公平，从而确保总量控制规划方案的顺利实施。     

Mosaicism for trisomy 12: Four cases with varying outcomes

Trisomy 12 observed in chorionic villus sampling (CVS) may reflect generalized mosaicism or indicate mosaicism confined to only the placenta. In this report, four cases of trisomy 12 observed in CVS or cultured placental biopsies with varying outcomes are presented. Seven dinucleotide repeat polymorphisms for chromosome 12 were used to determine the chromosome 12 origins in the fetus or child and to delineate the mechanism(s) that gave rise to the trisomy. In two cases (cases A and C), the mosaicism was confined to the placenta, resulting in normal liveborns. Although, in one case, the molecular results suggested an apparent duplication of one paternal chromosome 12 in the placenta, normal biparental inheritance was found in the diploid fetal cell line in both cases. In two other cases (cases B and D), trisomy 12 was observed in both extraembryonic and fetal tissues. In one of these pregnancies, a child was born by Caesarean section at 37 weeks because of intrauterine growth retardation and oligohydramnios, and resulted in neonatal death. Molecular markers and fluorescence in situ hybridization (FISH) revealed low-level trisomy 12 mosaicism in the spleen. In the fourth case, fetal abnormalities were detected on ultrasound and low-level trisomy 12 mosaicism was observed in amniotic fluid cells using conventional cytogenetics and FISH. Molecular markers revealed a maternal meiosis I non-disjunction of chromosome 12 in DNA from a cultured placental biopsy. Although predicting the outcomes of pregnancies involving confined placental mosaicism remains difficult, molecular techniques are valuable tools for distinguishing uniparental from biparental disomy and mechanisms of mosaicism.     

Evaluation of X,Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization

The major aneuploidies diagnosed prenatally involve the autosomes 13, 18, and 21, and sex chromosomes. Fluorescence in situ hybridization (FISH) allows rapid analysis of chromosome copy number in interphase cells. This prospective study evaluated the use of four commercially available centromeric DNA probes (DXZ1, DYZ1, D18Z1, and D13Z1/D21Z1) for direct analysis of uncultured amniocytes. One hundred and sixteen amniotic fluid samples were analysed by FISH and standard cytogenetics. This evaluation demonstrated that FISH with, X, Y, and 18 alpha satellite DNA probes could accurately and rapidly detect aneuploidies involving these chromosomes and could be used in any prenatal clinical laboratory. In contrast, the 13/21 alpha satellite DNA probe hybridizing both chromosomes 13 and 21 was unreliable for prenatal diagnosis in uncultured amniocytes.     

Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: A prospective study

A prospective study was undertaken to evaluate the use of fluorescence in situ hybridization (FISH) for the detection of trisomy 21 in interphase nuclei of uncultured amniotic fluid cells. Five hundred cases were analysed in situ and classified as normal or abnormal; the results were subsequently checked against the cytogenetic findings. Four hundred and ninety-three were correctly identified as normal with an 86·6 per cent average frequency of scored nuclei exhibiting two signals; six cases were correctly identified as trisomic for chromosome 21 with 81·7 per cent of scored nuclei exhibiting three signals; and one abnormal case involving an unbalanced chromosome 21·21 translocation was falsely scored as normal due to poor hybridization/detection efficiency. The method has been substantially improved and simplified so that it is suitable for the rapid detection of trisomy 21. As aneuploidy detection in interphase does not identify structural chromosome aberrations, it is not a substitute for fetal chromosome analysis.     

Molecular cytogenetic analysis of term placentae suspected of mosaicism using fluorescence in situ hybridization

In first-trimester chorionic villus sampling (CVS) for prenatal diagnosis, abnormal chromosomal findings, such as mosaicism, trisomies, or suspect abnormal karyotypes, are found more frequently than at amniocentesis. The fact that these chromosomal abnormalities do not always reflect the fetal karyotype but may be restricted to the placenta is a major problem in diagnosis and counselling. In this paper we present the results of fluorescence in situ hybridization (FISH) studies on interphase nuclei of three term placentae investigated because of false-positive findings at first-trimester CVS. The chorionic villi of the first case showed a mosaic chromosome pattern involving a trisomy 10 cell line and a normal cell line, those of the second case a total trisomy 8 cell line, while in the third case a complete monosomy X was found. Follow-up amniocentesis in each of these three cases revealed a normal karyotype. By using FISH, we were able to confirm the presence of the aberrant cell lines, which were all confined to one part of the placenta. FISH on interphase nuclei allows the investigation of large numbers of cells for the existence of numerical chromosome aberrations in a quick and reliable way.     

A complete set of procedure for determination of multiresidue of pesticides in vegetables

A complete set of procedure for determination of multiresidue of pesticides in vegetables was presented in this paper.The complete set of procedure included three steps:bioassay,cholinesterase inhibition and GLC analysis.The samples could be identified to be contaminated with pesticides if 5% of house flies was knocked down in 50 tested house flies. Those samples contaminated with pesticides needed to be detected by AChE inhibition method.The qualitative and quantitative analyses were carried out by GLC.Recoveries ranged from 83.7% in Chinese cabbages to 105.6% in tomatoes for pyrethroids,and 84.0% in tomatoes to 102.7% in sweetbell redpeppes for organophosphorus compounds.Coefficients of variations ranged from 0.59% to organophosphorus compounds.Coefficients of variations ranged from 0.59% to 7.87% for pyrethroids. and 0.33% to 9.88% for organophosphorus compounds with vegetables. The complete set of procedure has been used successfully to analyze 7000 samples collected in Beijing. About 1% of the samp     

农药污染环境质量评价

本文根据计算排毒系数的方法确定了主要污染源和污染物,又根据食入、饮进、呼吸等量建立了权重系统,由此而计算了中国不同农业区域的污染指数。结果表明,重污染区集中在长江、黄河流域的粮、棉产区,而且我国农业环境中BHC、DDT污染程度是向南或向北逐渐减弱。     

锡工业砷和铅排放标准的初步研究

根据污染源现场调研结果,结合现有污染控制工艺所能达到的技术水平,建议污水排放标准中As浓度由现国家排放标准的0 5mg/L调整为0 1mg/L;Pb不变为1 0mg/L。大气污染物排放标准中As和Pb不变为1 0mg/L。大气污染物排放标准As和Pb的浓度限值分别是为0 5mg/m3和0 7mg/m3。     

渭河宝鸡市区段阴离子表面活性剂污染研究

本文采用改进的亚甲蓝分光光度法，对渭河宝鸡市区段阴离子表面活性剂进行监测分析。测定结果表明：渭河在进入宝鸡市至植物园断面时阴离子表面活性剂含量较低，日平均值为0．049mg／L，达到地面水环境质量I类标准(≤0．2mg／L)(GB3838-88．地面水环境质量标准)；在流经市区新世纪桥、渭河桥断面时，由于分别有清姜河和金陵河两个支流的汇入，污染越来越严重．在这两个断面阴离子表面活性剂含量日平均值分别为0．34mg／L和0．54mg／L；在即将流出宝鸡市的斗鸡断面阴离子表面活性剂含量日平均值为0．424mg／L，已远远超过地面水环境质量V类标准(≤0．3mg／L)(GB3838-88，地面水环境质量标准)。从监测结果看：双休日阴离子表面活性剂含量普遍高于工作日；清姜河、金陵河污染严重，这两条支流的汇入对渭河水质影响巨大，要治理好渭河，须先治理好清姜河和金陵河这两条支流。     

腈纶粉尘对作业工人健康影响的调查

为探讨腈纶粉尘对作业工人健康的影响,对某腈纶厂毛条车间进行了劳动卫生学调查.该车间粉尘浓度为4.2(0.1～24)mg/m3,主要对接触人员上呼吸道和皮肤有刺激作用,同时导致肺通气功能受到明显损伤,部分工人胸部X线表现异常.提示车间环境中时间加权平均容许浓度超过2mg/m3、短时间接触容许浓度超过4mg/m3尘的卫生标准不能充分保护工人健康.