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51.
青岛港在环渤海港口群中处于重要地位,目前已与大连港、天津港形成了我国北方地区“三港鼎立”的格局.从分析青岛港发展现状与存在问题出发,比较评价了环渤海地区主要港口的竞争力,分析青岛港发展中的竞争优势与不足,探寻提升青岛港港口竞争力的途径与对策. 相似文献
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北京、东京、筑波大气中有机污染物组成研究 总被引:28,自引:0,他引:28
用低流量采样器及双层采样滤膜 (石英及固相萃取用C1 8膜 )采集了北京、东京和筑波三城市冬季 (1999年 1月 )大气颗粒物和大气气相物质 ,3个城市的共同特点是大气气相物质中含有很高浓度的苯环数 2~ 4的多环芳烃及碳数小于 2 0的正构烷烃 ,大气颗粒物中以 5~ 6个苯环多环芳烃为主。冬季正构烷烃没有明显的偶数碳数和奇数的区别。但是 ,北京大气气相物质和颗粒物中多环芳烃浓度明显高于东京和筑波 ,而且各正构烷烃及多环芳烃的浓度分布也与东京和筑波的不同 ,表明冬季大气中有机污染物来源不同。 相似文献
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IntroductionItwasbelievedthatonlyhigh_levelnoisecouldcausenoisepollution.Theinfluenceoflow_levelnoisehasnotbeenwidelynoticed.Thisresearchdiscoveredthatundercertainconditionsthelow_levelnoise,especiallylowfrequencynoise,mayevencausehigherannoyanceresponse.… 相似文献
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S. McLean MD W. Stanley H. Stern J. Fonda-Allen G. Devine T. Ellingham K. Rosenbaum 《黑龙江环境通报》1992,12(12):985-991
We report a case of Pallister-Killian syndrome initially diagnosed prenatally as tetrasomy 21. A 33-year-old primiparous woman was noted at 24 weeks' gestation to have moderate polyhydramnios. Ultrasonography showed diminished fetal stomach filling, hydronephrosis, and prominence of the cisterna magna. Cytogenetic analysis of cultured amniocytes was initially interpreted as mosaic tetrasomy 21: 46,XX/47,XX,+i(21q). The patient was then referred to our centre for genetic counselling. At 34 weeks' gestation, a dysmorphic infant was delivered and died within 30 min. Physical features were consistent with the Pallister-Killian syndrome. Renal, gastrointestinal, and central nervous system anomalies were found at post-mortem examination. Analysis of peripheral lymphocytes revealed 5 per cent of cells with a marker chromosome, while 92 per cent of cultured fibroblasts had this same marker. Fluorescent in situ hybridization (FISH) using an alpha-satellite probe for chromosomes 13 and 21 failed to hybridize to the marker, while a chromosome 12 centromeric probe unequivocally identified it as an i(12p). Use of FISH can provide rapid, specific prenatal diagnosis of ambiguous marker chromosomes and improve prenatal counselling. 相似文献
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Data on chromosomal mosaicism was collected retrospectively on 12 386 amniotic fluid samples cultured over a 10 year period in 14 Canadian centres. Level I mosaicism (a single abnormal cell—excluding single cell monosomy) was encountered in 863 cases (7.1 per cent). Level II mosaicism (multiple cells with the same abnormality in a single flask or colony) was encountered in 138 cases (1.1 per cent). Level III mosaicism (multiple cells distributed over multiple flasks or colonies) was encountered in 34 cases (0.3 per cent). Analysis of the details of these cases allowed five major conclusions to be drawn: (1) Single cell abnormalities should not be taken as an indication of true fetal mosaicism. Only rarely will this interpretation prove to be incorrect. (2) Mosaicism involving multiple cells confined to a single flask should not be regarded as an indication of true fetal mosaicism. Only occasionally will this interpretation prove to be incorrect. (3) Mosaicism involving multiple cells distributed over more than one flask should be regarded as a strong indication of true fetal mosaicism. Sixty per cent will be confirmed by karyotype analysis of the fetus or infant. (4) Mosaicism of the XX/XY type is usually due to maternal cell contamination. Occasionally it can be a female fetus with XY cells from an unknown source. (5) The in situ or colony method of chromosome analysis has no clear advantage over the flask method for either the detection of true fetal mosaicism or for the ability to distinguish true mosaics from false positives. 相似文献