规划环境影响评价中公众参与有效性的探讨

公众参与在规划环境影响评价中具有重要的意义。目前环境影响评价中公众参与中存在许多不足，严重影响了公众参与的有效性，在提高规划环境影响评价中公众参与制度的有效性、信息发布的有效性、参与对象的有效性、参与方法的有效性以及结论有效性等方面提出了建议。     

我国可持续设计及其实践的探讨

可持续设计超越了传统设计和生态设计，要求平衡经济、环境、社会３方面的发展需要，在可持续设计的基本工具产品生命周期评价尚需进一步发展的同时，建立适当的设计准则是当前发展可持续设计的可行途径。     

有机磷酸酯诱导迟发性神经毒性及其对神经毒性酯酶(NTE)活性影响的动态研究

以成年产卵来航母鸡为试验动物，研究了三甲基苯基磷酸酯诱导的迟发性神经毒性。试验发现，母鸡口服ＴＯＣＰ后经过大约８－１０ｄ的潜伏期开始出现中毒症状，其表现为以步态失调为主要特征的运动障碍呈进行性加重，至２１ｄ开始便发展为瘫痪。     

MSAFP levels and oesophageal atresia

This study was undertaken to evaluate the relationship between maternal serum alpha-fetoprotein (MSAFP) levels and oesophageal atresia (OA). OA occurred in 16 fetuses of mothers who had an MSAFP test in the study interval. The multiple of the median (MOM) value for MSAFP averaged 1·54 ± 0·65 (range 0·5–2·9 MOM), which was significantly higher than the value seen in controls. The median MOM was 1·35. Using a cut-off of 2·5 MOM, the sensitivity of MSAFP for detecting OA was 19 per cent. Although OA should be considered in the differential diagnosis of an elevated MSAFP level, MSAFP cannot be considered an appropriate screening test for OA given the low sensitivity.     

Achondrogenesis type 2 diagnosed by transvaginal ultrasound at 12 weeks' gestation

Ultrasound examination at 12 weeks' gestation revealed severe generalised subcutaneous oedema in a pregnancy at risk for achondrogenesis type II. Transvaginal scanning confirmed the oedema and suggested abnormal limb development. The prenatal diagnosis was confirmed by X-ray examination after transvaginal termination.     

Dystrophin protein and rflp analyis for fetal diagnosis and carrier confirmation of duchenne muscular dystrophy

A pregnant woman with indeterminate Duchenne muscular dystrophy (DMD) carrier status, but with DMD diagnosed in her deceased brother (unavailable for study), presented for prenatal diagnosis, intending to continue the pregnancy only if proven unaffected with DMD with near absolute certainty. Creatine kinase (CK) assays to clarify carrier status were inconclusive. Male sex in the fetus was identified, but DNA restriction fragment length polymorphism (RFLP) analysis was not yet available to this centre to investigate the possible transmission of the DMD gene, and the pregnancy was terminated. Tissue histology and dystrophin protein analysis demonstrated the absence of DMD. In a situation with proven maternal carrier status, future fetal inheritance of the opposite maternal X chromosome would indicate the presence of DMD. However, maternal carrier status remained in doubt through a second pregnancy, even with RFLP studies, and was finally established when dystrophin analysis confirmed the presence of DMD in the second fetus. Histologic findings are presented, contrasting features in the two fetuses. The value of dystrophin analysis for establishing the diagnosis of fetal DMD, in this case proving maternal carrier status in a difficult situation, and for demonstrating DMD gene:RFLP haplotype relationships is illustrated.     

Service transformation—managing a shift from business travel to virtual meetings

It has been shown that the potential for environmental, and financial improvements through the increased substitution of in-person meetings by virtual communication is considerable. However, it has also been shown that this potential is not automatically realized by investing in the technology that can enable virtual meetings. This paper describes two case studies that explored the factors that influenced communication and meeting behavior. A number of drivers and barriers for virtual meetings are identified, and, in addition, measures are proposed to improve the utilization of virtual tools for business communication.     

大连湾陆源污染物排海总量控制信息系统概念设计

根据陆源污染物总量控制原理和沿海地区地方政府的经济条件，以大连湾为例，采用地理信息系统（ＧＩＳ）技术，设计了排放入海湾的陆源污染物总量控制信息系统的概念模型，涉及系统建设的原则，数据类型，软件，硬件，用户界面和功能。为我国海湾污染物控制工作提供经济实用，先进的管理方法。     

Prenatal diagnosis of Opitz (BBB) syndrome in the second trimester by ultrasound detection of hypospadias and hypertelorism

Prenatal diagnosis in a kindred with the Opitz (BBB) syndrome is presented. The inheritance is consistent with either autosomal dominant inheritance with sex limited expression or X-linked inheritance. The abnormalities in the kindred consist of hypertelorism, hypospadias, ambiguous genitalia, urocolic fistula, imperforate anus, mental retardation, diaphragmatic hernia, and malrotation with volvulus. A male fetus at 19 weeks was found by ultrasound to have hypertelorism and hypospadias with a small phallus consistent with the syndrome. The diagnosis was confirmed by pathologic examination after pregnancy termination. This is the first report of prenatal diagnosis of Opitz syndrome by ultrasonographic demonstration of hypertelorism and hypospadias in the second trimester.     

主次波长新分光光度法测定天然水硝酸盐

在硫酸介质中,邻苯氨基苯甲酸与硝酸盐(NO_3~-)生成紫红色络合物.本文依据悬浮颗粒对光的吸收性质研究利用该灵敏反应测定 NO_3~—N 新光度法——(?)次双波长法,通过对样品分析,可提高分析灵敏度和精密度,回收良好,且操作简单快速,计算曲线稳定,适合于测定地下水,湖水等天然水体 NO_3~-—N.