Analysis of health or systemic effects caused by two toxicants

A method is presented for the analysis of the risk to man or other systems by effects caused by a combination of two insults. The approach is purely phenomenological and has no built-in restrictions other than those required by logic and those imposed by the limited set of trial functions. The analysis attempts to isolate the dominant contributions to the risks from either agent alone and from both agents in combination. To demonstrate the viability of the method, it is applied to the analysis of human health data on oral and esophageal cancer correlated with alcohol and tobacco consumption. For both cancers, it is found that the most probable form of the relative risk is separable into a factor related to tobacco and one related to alcohol. Both have the same algebraic form and the values of the risk coefficients are practically equal. An analysis of analogous but limited data on laryngeal cancer cannot assign an algebraic form of the risk function but still yields comparable risk coefficients. Thus it is possible that all three cancers have the same risk function as a function of alcohol and tobacco consumption.     

铁路行车事故救援智能辅助决策系统研究

介绍了铁路行车事故救援智能辅助决策系统的设计及实现。采用产生式规则与数据库技术相结合的铁路行车事故救援决策知识表示方法。推理过程为正向推理。决策树分层分类并嵌入数据库。该系统可在行车事故现场以人机交互方式提供一个或几个救援方案。为铁路行车事故救援决策提供了一种新的途径与范例。并为人工智能在新的工程领域的应用进行了有益的尝试     

矿井热害产生的原因、危害及防治措施

随着矿井开采深度的增加 ,矿井中高温高湿热害问题会越来越严重。笔者分析了矿井中高温高湿热害产生的具体原因、对人体的严重危害 ,并探讨了对其防治的相应措施 ,建立井下适宜的作业环境 ,保护矿工的身体健康 ,保证矿山生产安全、稳定、高效地向前发展。笔者旨在提醒人们对矿井中高温高湿热害这个问题引起重视 ,尽量减少其对人体的危害 ,采取一切有效办法 ,尽快解决矿井中高温高湿热害问题     

Life-history patterns of two Southern CaliforniaNebalia species (Crustacea: Leptostraca): the failure of form to predict function

Laboratory and field studies onNebalia hessleri andN. daytoni off the toast of San Diego, Southern California, showed that although morphologically similar, the habitats, behavior, and natural history of these two species are surprisingly different. In laboratory experiments, Bach species avoided the other's habitat (sand and mats of macrophyte detritus), and in the field, transplanted individuals failed to survive in the other species' habitat.N. hessleri, which inhabits subtidal mats of macrophyte detritus, survived and reproduced well in the laboratory, was iteroparous, and a large percentage of adults were male. This species occurred at very high densities in the field, and ate essentially everything offered in the laboratory, with a diet in the field consisting largely of plant detritus and carrion. The other species,N. daytoni, differed in nearly every way, it inhabited organically impoverished sands, survived poorly in the laboratory, was apparently semelparous, and a small percentage of the adult population was male.     

Detection of trisomy 21 by quantitative fluorescent–polymerase chain reaction in uncultured amniocytes

Prenatal diagnosis of fetal trisomy 21 is usually performed by cytogenetic analysis. This requires lengthy laboratory procedures, high costs and is unsuitable for large-scale screening of pregnant women. Today, trisomy 21 can be rapidly diagnosed within 24 h by molecular analysis of uncultured fetal cells using the semi-quantification of fluorescent PCR products from short tandem repeat (STR) polymorphic markers. The aim of our study was to test a chromosome quantification method on the basis of the analysis of fluorescent PCR products derived from non-polymorphic target genes. Co-amplification of a portion of DSCR1 (Down syndrome Critical Region 1) and the reference gene, CFTR (cystic fibrosis transmembrane regulator) enabled molecular detection of trisomy 21. Our method was successfully tested on a total of 154 amniotic fluids in a blind prospective study. Calculation of the DSCR1/CFTR ratio allowed us to distinguish between 152 normal amniotic fluids (mean ratio 0.99) and 2 amniotic fluids presenting a trisomy 21 status (DSCR1/CFTR ratio of 1.53 and 1.61, respectively). The results obtained by conventional cytogenetic analysis and our quantitative PCR method were concordant in every case. Our gene-based fluorescent PCR approach represents an alternative molecular method for rapid and reliable detection of trisomy 21, which can be helpful in the prenatal diagnosis of women at high risk of fetal trisomy 21. Copyright © 2003 John Wiley & Sons, Ltd.     

Molecular genetic prenatal diagnosis for a case of autosomal recessive spondylocostal dysostosis

Autosomal recessive spondylocostal dysostosis type 1 (ARSCD1) is a member of the heterogeneous group of disorders termed the spondylocostal dysostoses that are characterized by multiple vertebral segmentation defects and rib anomalies. In these patients, the entire vertebral column is malformed and is replaced by multiple hemivertebrae giving rise to truncal shortening, abdominal protrusion and non-progressive spinal curvature. Genetic studies have shown that some cases of ARSCD are due to mutations in the somitogenesis gene, Delta-like 3 (DLL3), that encodes a ligand for the Notch signalling pathway—ARSCD type 1. To date, 17 different DLL3 gene mutations have been reported. A consanguineous family of Turkish origin with ARSCD type 1 due to a homozygous DLL3 mutation requested genetic prenatal diagnosis. Using DNA from a chorionic villus sample, both linkage analysis of the DLL3/19q region and direct sequencing for the familial mutation demonstrated that the unborn fetus was an unaffected carrier. This is the first case of molecular genetic prenatal diagnosis in any form of SCD. Copyright © 2003 John Wiley & Sons, Ltd.     

Tests appropriate for the prenatal diagnosis of ataxia telangiectasia

A fetus ‘at-risk’ for ataxia telangiectasia (A-T) was monitored prenatally by several approaches which, in concert, might yield information of diagnostic value: measurement of amniotic fluid AFP levels; the clastogenic potential of ‘at-risk’ amniotic fluid; and cytogenic evaluation of fetal amniocytes. All three parameters proved negative and normality, based primarily on the chromosomal study of fetal cells, was therefore presumed. This conclusion was confirmed shortly after birth by normal serum AFP levels and the lack of increased spontaneous or clastogen-induced chromosome breakage in the infant's cells. Based on previous observations from four normal and one affected fetus, the coordination of these techniques provides adequate methodology for the antenatal assessment of the phenotypes associated with A-T.     

非线性理论在开采沉陷中的应用

简要介绍了近年来把非线性理论应用于矿山开采沉陷领域的一些研究成果,主要包括两大部分：（１）神经网络理论在开采沉陷中的应用;（２）离散单元法在开采沉陷中的应用