利用InSAR监测矿山采空区地表沉降的过程中易在沉降中心周围产生失相干现象,导致形变结果缺失,无法获取准确的沉降区模型。基于此,提出了一种结合时序InSAR与PIM(Probability Integral Method)的监测方法,以云南省玉溪市大红山铁矿地下...利用InSAR监测矿山采空区地表沉降的过程中易在沉降中心周围产生失相干现象,导致形变结果缺失,无法获取准确的沉降区模型。基于此,提出了一种结合时序InSAR与PIM(Probability Integral Method)的监测方法,以云南省玉溪市大红山铁矿地下采区某工作面为研究对象,首先计算出时序InSAR累积沉降量,并提取其沉降区边缘的高相干点,结合少量沉降中心水准点,利用改进型PSO(Particle Swarm Optimization)算法获取PIM参数,并通过克里金插值法建立采空区地表整体沉降区模型,利用少量水准点数据对该方法的可靠性和精度进行验证,结果表明,该方法获得的沉降区分布与实际相吻合,其沉降区监测精度比单独使用时序InSAR或PIM的更高,可用于矿区地表沉降信息的准确获取。展开更多
Although ge ne tic algorithm has become very famous with its global searching, parallel computi ng, better robustness, and not needing differential information during evolution .However, it also has some demerits, suc...Although ge ne tic algorithm has become very famous with its global searching, parallel computi ng, better robustness, and not needing differential information during evolution .However, it also has some demerits, such as slow convergence speed. In this pap er, based on several general theorems, an improved genetic algorithm using varia nt chromosome length and probability of crossover and mutation is proposed, and its main idea is as follows:at the beginning of evolution, our solution with sho rter length chromosome and higher probability of crossover and mutation; and at the vicinity of global optimum, with longer length chromosome and lower probabil ity of crossover and mutation. Finally, testing with some critical functions sho ws that our solution can improve the convergence speed of genetic algorithm sign ificantly, its comprehensive performance is better than that of the genetic algo rithm which only reserves the best individual.展开更多
A five-year old Iraqi patient with beta thalassemia major was presented with recurrent attack of Bell's palsy on 2 successive years being a milder one in the second year. This is a rare occurrence in beta thalassemia...A five-year old Iraqi patient with beta thalassemia major was presented with recurrent attack of Bell's palsy on 2 successive years being a milder one in the second year. This is a rare occurrence in beta thalassemia major patients and needs to be further explored. This is a case report of a nine-year old Iraqi child who is the only child born to parents of secondary consanguinity relatives from Babil Province who was diagnosed as beta thalassemia on the age of 6 months and is on regular blood transfusion and iron chelation therapy of deferasirox tablets (Exjade), his medical follow up takes place at Babil Thalassemia center in Babil Maternity and Child Hospital. On the age of five years, he was presented with a sudden onset of right sided Bell's palsy within twenty four hours of swimming in a cool swimming pool at his home in July 2011. A neurosurgeon examined him at that time, no investigations were done, the diagnosis was purely clinical, steroid & neurotonics were recommended as a treatment for the condition, antiviral agents were not prescribed, lacrimation & taste were not affected, there was a slow improvement, two weeks later physiotherapy sessions including facial massage ad electric stimulation were recommended after which the child improved. The next year, another attach of Bell's Palsy developed at a similar time with the same sequel of events, this time the attack was milder and with residual effects seen in the eye & mouth. This coincidence of beta thalassemia and Bell's palsy should be further studied by observational epidemiologic studies to prove or disprove the hypothesis that thalassemic patients especially children are at higher risk of developing Bell's palsy than healthy children. Beta thalassemia patients may be at higher risk of developing Bell's Palsy.展开更多
文摘利用InSAR监测矿山采空区地表沉降的过程中易在沉降中心周围产生失相干现象,导致形变结果缺失,无法获取准确的沉降区模型。基于此,提出了一种结合时序InSAR与PIM(Probability Integral Method)的监测方法,以云南省玉溪市大红山铁矿地下采区某工作面为研究对象,首先计算出时序InSAR累积沉降量,并提取其沉降区边缘的高相干点,结合少量沉降中心水准点,利用改进型PSO(Particle Swarm Optimization)算法获取PIM参数,并通过克里金插值法建立采空区地表整体沉降区模型,利用少量水准点数据对该方法的可靠性和精度进行验证,结果表明,该方法获得的沉降区分布与实际相吻合,其沉降区监测精度比单独使用时序InSAR或PIM的更高,可用于矿区地表沉降信息的准确获取。
文摘Although ge ne tic algorithm has become very famous with its global searching, parallel computi ng, better robustness, and not needing differential information during evolution .However, it also has some demerits, such as slow convergence speed. In this pap er, based on several general theorems, an improved genetic algorithm using varia nt chromosome length and probability of crossover and mutation is proposed, and its main idea is as follows:at the beginning of evolution, our solution with sho rter length chromosome and higher probability of crossover and mutation; and at the vicinity of global optimum, with longer length chromosome and lower probabil ity of crossover and mutation. Finally, testing with some critical functions sho ws that our solution can improve the convergence speed of genetic algorithm sign ificantly, its comprehensive performance is better than that of the genetic algo rithm which only reserves the best individual.
文摘A five-year old Iraqi patient with beta thalassemia major was presented with recurrent attack of Bell's palsy on 2 successive years being a milder one in the second year. This is a rare occurrence in beta thalassemia major patients and needs to be further explored. This is a case report of a nine-year old Iraqi child who is the only child born to parents of secondary consanguinity relatives from Babil Province who was diagnosed as beta thalassemia on the age of 6 months and is on regular blood transfusion and iron chelation therapy of deferasirox tablets (Exjade), his medical follow up takes place at Babil Thalassemia center in Babil Maternity and Child Hospital. On the age of five years, he was presented with a sudden onset of right sided Bell's palsy within twenty four hours of swimming in a cool swimming pool at his home in July 2011. A neurosurgeon examined him at that time, no investigations were done, the diagnosis was purely clinical, steroid & neurotonics were recommended as a treatment for the condition, antiviral agents were not prescribed, lacrimation & taste were not affected, there was a slow improvement, two weeks later physiotherapy sessions including facial massage ad electric stimulation were recommended after which the child improved. The next year, another attach of Bell's Palsy developed at a similar time with the same sequel of events, this time the attack was milder and with residual effects seen in the eye & mouth. This coincidence of beta thalassemia and Bell's palsy should be further studied by observational epidemiologic studies to prove or disprove the hypothesis that thalassemic patients especially children are at higher risk of developing Bell's palsy than healthy children. Beta thalassemia patients may be at higher risk of developing Bell's Palsy.