浅议农业源和生活源对长桥海的影响

通过对蒙自下游长桥海水质状况和主要污染源农业源、生活源的分析,提出污染控制对策。     

浅谈如何确定总量排污收费试点征收标准

通过一年的总量排污收费实际征收，本文用实践经验，从确定征收标准的原则、 测算样本、数据的统计分析三方面，结合郑州市的实际情况，对水污染物和大气污染物征收标准的确定进行了探讨， 特别是在数据的统计分析方面，通过不同的统计方法计算出不同的统计结果，说明了制定统计方法的重要性，提出了科学合理的统计分析方法。同时简述了确定试点征收标准时应注意的一些问题。     

胶州湾潮间带和沿岸区硫酸盐还原菌含量分布

用 Ｍ Ｐ Ｎ 法对胶州湾潮间带和沿岸区的硫酸盐还原菌（ 缩写为 Ｓ Ｒ Ｂ） 含量作了研究，结果表明表层沉积物的 Ｓ Ｒ Ｂ 含量大约是４１ ×１０７ 个细胞／ｇ ，波动范围较大。水中的 Ｓ Ｒ Ｂ 含量约２５ ×１０２／ｍｌ。分析了 Ｓ Ｒ Ｂ 含量的分布状况，发现调查区内的 Ｓ Ｒ Ｂ 含量基本上呈现出北高南低、西高东低之势，即工业区、港口区的高于海水浴场、海滨旅游区的。证实了生活废弃物的排放致其环境 Ｓ Ｒ Ｂ 含量特高。 Ｓ Ｒ Ｂ 含量分布状况大体上与以往所测环境污染状况一致。对虾养殖池的 Ｓ Ｒ Ｂ 含量意味着水产养殖必须考虑这一因子的作用     

噪声的污染与治理

介绍了大庆石化总厂化工二厂生产装置的噪声污染情况，防治措施。对今后噪声治理提出了设想．     

可转让排污许可证制度立法研究

在市场经济条件下,对符合法定条件的排污许可证应当允许其有偿转让。可转让的排污许可证必须以污染物申报登记为基础,以污染物总量控制为前提,以环境标准为依据,转让活动应当在政府严格监督下进行。可转让排污许可证制度通过市场机制和价值规律必将有效地促进污染防治。     

Fetal cholecystomegaly: A prenatal marker of aneuploidy

The fetal gall bladder can now be easily identified during the second and third trimesters using high-resolution ultrasonography. In this report we present eight fetuses with an enlarged gall bladder detected on prenatal ultrasonography at a mean gestational age of 24.6 weeks (range 19–31 weeks). Additional ultrasonographic findings were present in four cases: fetal anomalies and intrauterine growth retardation in three and polyhydramnios in one. Of those cases associated with fetal anomalies, one woman underwent amniocentesis at 21 weeks revealing trisomy 18. The other two declined prenatal karyotyping; neonatal karyotyping revealed trisomy 13 in one and trisomy 18 in the other. Although an enlarged fetal gall bladder can be a normal variant in the second and third trimesters, the prenatal detection of cholecystomegaly should prompt a search for associated anomalies and other markers of aneuploidy. If found, prenatal karyotyping should be considered.     

Prenatal diagnosis of mosaic 4p – in a fetus with trisomy 21

Mosaicism for the Wolf-Hirschhorn syndrome, del(4)(p16), is extremely rare and has not been reported in association with a numerical chromosome abnormality. We report the prenatal diagnosis of mosaic del(4)(p16) and non-mosaic trisomy 21 in a 16-week female fetus. The pregnancy ended in spontaneous abortion at 34 weeks secondary to fetal demise. The fetus had features of both 4p – and trisomy 21.     

An investigation of methods for enriching trophoblast from maternal blood

Trophoblast deportation is known to occur in normal human pregnancy, but it is not yet clear whether these cells routinely enter the maternal peripheral circulation and are available as a source of fetal DNA for non-invasive prenatal diagnosis of genetic disorders. To resolve this issue requires an efficient method of enriching trophoblast from maternal blood combined with a means to confirm its identity. Five different techniques were tested on ten retroplacental blood samples to determine the most sensitive and operator-efficient method. Lysis of red cells alone gave the best recovery of trophoblast but had to be discounted, together with Ficoll density gradient centrifugation, due to the very low purity and the excessive time required. Fluorescence-activated cell sorting (FACS) of pre-enriched trophoblast resulted in the lowest recovery rate (8 per cent) despite a 3250-fold enrichment and a very high purity. Immunomagnetic beads (Dynabeads) coated with anti-CD 16 antibody proved to be the best method for the subsequent immunocytochemical characterization of deported trophoblast. However, IO beads coated with anti-CD45 antibody may be more useful for isolating trophoblast for prenatal diagnosis due to the high purity, enrichment (32-fold), and recovery rate (78 per cent) obtained with this method.     

Prenatal exclusion of stickler syndrome

Stickler syndrome is an autosomal dominant disorder of the connective tissue which includes ocular and systemic manifestations. We report on a large kindred in which we were able to demonstrate very tight linkage between the disease and the type II collagen gene (COL2A1) (LOD score 3·91 at θ=0). In a family in which the father and one of his daughters were severely affected, DNA analysis from a chorionic villus sample demonstrated that the fetus possessed the normal allele of COL2A1. Thereafter a normal child was born.     

Prenatal diagnosis of congenital gastric outlet obstruction

A case of gastric outlet obstruction diagnosed prenatally at 22 weeks' gestation is described. The differential diagnosis and the clinical management of this rare condition are discussed, and an updated literature review is presented.