科技促进宁夏可持续发展的现状分析

科技是推动宁夏进一步深化改革与发展、实施西部大开发战略、促进经济持续增长、优化产业结构、提升产业竞争实力、缓解发展过程中的资源环境约束力、实现可持续发展的核心力量.科技在促进宁夏实现可持续发展方面取得显著的成就与经验,但是在支Ё撑全区社会经济发展、改善环境以及区域科技创新能力建设方面仍存在急需解决的问题:①科技资源布局不合理;②产业工艺落后,能耗偏高:③特色优势产业发展后劲严重不足,成果转化率低;④区域科技创新能力弱.文章最后结合宁夏自然环境条件、社会经济发展状况、文化特点提出了其未来科技发展的战略思路及重点.     

新西兰无过失伤害的预防、康复和赔偿体制介绍

新西兰意外赔偿局(ACC),是管理新西兰意外事件赔偿的政府机构。ACC计划是对在新西兰境内的公民、居民或临时来访的人提供受伤赔偿的服务。每年在复原、治疗和酬劳补偿等方面要花费十几亿元,为了保证这些服务,ACC从劳动者的薪金、燃油税、政府赞助和投资收入等方面来支付赔偿金,不同行业的工伤赔偿申请比率也不同。另外,ACC建立了培训基金,代替雇主负责对员工的安全与健康培训。虽然这一体制正面临一些私有化和费用不断增加的挑战和困难,但总体来说,ACC体制是适合新西兰的一个优良的方案,比其他国家的体制在管理效率和雇主利益等方面明显显示出优势。     

Local Area Quotas for Industrial Emissions along Reaches of the Pearl River in Guangdong

There is an obvious departure from the regional equilibrium of developments between the upper and lower reaches of the Pearl River in Guangdong, which resulted in ＂the effects of contra-geography-grads development＂. It is mainly because the upriver mountainous areas have been deeply stuck in industrialization delay and marginalization plights, so that nearly 40 million local people have conceived a dream to get rid of ＂the vicious circle of poverty＂ by speeding up industrial development. But the problem is that such industrialization efforts on a large scale in mountainous areas are encountering the bottleneck of environmental capacity that strictly limits industrial emissions along the upper reaches of any water system. As a solution, an institutional arrangement called ＂the Local Area Quotas for Industrial Emissions along the Pearl River＂ is put forward supposed to give corresponding compensation to the rights of industrial development yielded by some areas with lower environmental capacity through the distribution and trading of IDQs.     

薄层色谱紫外分光光度法定量测定微生物发酵产物辅酶Q10

报道了一种微生物发酵液中辅酶Q10的定量检测方法.该方法分为两个步骤:第一步是离心收集菌体和结合使用超声波处理的辅酶Q10丙酮抽提;第二步是硅胶薄层色谱,根据标样位置取产物斑点乙醇洗脱后用紫外分光光度法测定辅酶Q10含量.结果表明,该方法具有操作简便、重复性好、相对误差小等优点,可用于细菌发酵生产辅酶Q10研究过程中发酵产物的快速定量检测.图2表2参6     

Del(18p) syndrome with increased nuchal translucency in prenatal diagnosis

We report a de novo translocation between chromosome 15 and 18 resulting in monosomy 18p in prenatal diagnosis. The patient was referred for amniocentesis due to increased nuchal translucency (INT) (5 mm) at 13.6 weeks of gestation. Karyotype of the fetus revealed 45,XX,der(15;18)(q10;q10) in all metaphases. The targeted fetal ultrasound at 20 weeks of gestation did not show any special physical abnormalities other than 6.4 mm of nuchal fold thickness. Molecular cytogenetic findings using CGH and FISH confirmed the del(18p) with dicentromeres from both chromosome 15 and 18. The present study shows that the INT at first trimester was the only prenatal finding for the fetus with del(18p) syndrome and that molecular cytogenetic methods are useful for detecting chromosomal aberrations precisely. Copyright © 2004 John Wiley & Sons, Ltd.     

Intrauterine left chamber myocardial infarction of the heart and hydrops fetalis in the recipient fetus due to twin-to-twin transfusion syndrome

A rare complication of twin-to-twin transfusion syndrome (TTTS) is described: myocardial infarction of the recipient fetus. Myocardial infarction and hydrops are considered to be consequences of hypertension in the recipient. No other organs were affected. Pathological signs of intrauterine hypertension were estimated by the thickness of vessel walls and signs of hypertrophied myocardial cells. In the heart of the recipient fetus there was a chronic myocardial infarction near the apex cordis on the anterior wall with an aneurysm 4×5 mm in diameter. Diagnosis was based on light microscopic examination. The poor myocardial systolic function resulted in hydrops. Since the mother was administered β sympathomimetics in therapeutic doses the contribution of the drug to the myocardial infarction is uncertain, but we would like to suggest this as a possible adverse effect in TTTS. The present case is the first reported myocardial infarction in connection with the syndrome. Copyright © 2002 John Wiley & Sons, Ltd.     

Preimplantation genetic diagnosis for familial amyloidotic polyneuropathy (FAP)

Preimplantation genetic diagnosis (PGD) was developed more than a decade ago to offer an alternative to prenatal diagnosis for couples at risk of transmitting an inherited disease to their offspring. Portuguese-type familial amyloidotic polyneuropathy (FAP type I), is an autosomal dominant disease presenting an inherited mutation in the gene encoding the plasma protein transthyretin (TTR). We here report the first protocol for single-cell detection of the Met30 mutation in FAP type I and its application to PGD. A nested PCR reaction for exon 2 of the TTR gene was developed. The PCR product was then analysed by restriction enzyme analysis and SSCP allowing the detection of the point mutation. Ten clinical cycles were performed in seven couples. From the 93 metaphase II (MII) injected oocytes, 82 were normally fertilized and 78 were biopsied. A positive signal in the nested PCR reaction was obtained in 61 blastomeres, corresponding to a DNA amplification efficiency of 78.2%. No allele dropout (ADO) or contamination were detected. A biochemical pregnancy was obtained in three cases and a clinical pregnancy in one couple is actually in normal evolution. Copyright © 2001 John Wiley & Sons, Ltd.     

基于高程的环境库兹涅茨曲线实证分析

本文利用GIS的空间分析技术。以高程带为取样单元。研究在高程带上三种主要的大气污染物与经济发展之间的定量关系。以重庆市为例,验证环境库兹涅茨在高程上是否存在。研究结果发现。污染物浓度随高程的增加呈非单调下降的趋势。人均GDP随高程的增加先增大后减小。在高程上。污染物浓度与经济发展之间的关系和两者在时间序列和国别（或地区）序列上环境库兹涅茨曲线研究的结论相似。其中。TSP和NOx分别与人均GDP之间呈较稳定的呈“N”形和饲“U”形关系。受人口密度和高程影响较大；而SO2与人均GDP之间关系不稳定。