基于扩展度的复杂网络传播影响力评估算法

对网络中节点的传播影响力进行评估具有十分重要的意义, 有助于促进有益或抑制有害信息的传播. 目前, 多种中心性指标可用于对节点的传播影响力进行评估, 然而它们一般只有当传播率处于特定范围时才能取得理想的结果. 例如, 度值中心性指标在传播率较小时较为合适, 而半局部中心性和接近中心性指标则适用于稍大一些的传播率. 为了解决各种评估指标对传播率敏感的问题, 提出了一种基于扩展度的传播影响力评估算法. 算法利用邻居节点度值叠加的方式对节点度的覆盖范围进行了扩展, 使不同的扩展层次对应于不同的传播率, 并通过抽样测试确定了适合于特定传播率的层次数. 真实和模拟数据集上的实验结果表明, 通过扩展度算法得到的扩展度指标能在不同传播率下对节点的传播影响力进行有效评估, 其准确性能够达到或优于利用其他中心性指标进行评估的结果.     

一种新的卫星钟差Kalman滤波噪声协方差估计方法

采用Kalman滤波方法进行钟差参数计算和预报时, 需确定Kalman滤波噪声协方差矩阵. 针对这一问题, 提出了一种新的卫星钟差Kalman滤波噪声协方差估计方法, 通过建立新息的相关函数序列与未知的噪声参数间的线性函数模型, 采用最小二乘法进行噪声参数估计. 采用精密钟差数据进行钟差参数估计和预报分析, 结果表明, 该方法具有较好的收敛性, 并与顾及随机噪声模型的开窗分类因子自适应抗差估计方法进行对比分析, 验证了新方法的正确性和有效性.     

Single top partner production in the tZ channel at eγ collision in the littlest Higgs model with T-parity

Introducing the top partner is a common way to cancel the largest quadratically divergent contribution to the Higgs mass induced by the top quark. In this work, we study single top partner production in the tZ channel at eγ collision in the littlest Higgs model with T-parity(LHT). Since it is well known that polarized beams can enhance the cross section, we analyze the signal via polarized electron beams,and photon beams. we have selected two decay modes for comparison, based on the leptonic or the hadronic decays of the W and Z from the top partner. We then construct a detailed detector simulation, and choose a set of cuts to enhance signal significance. For mode A(B), the capacity for exclusion in this process at s~(1/2)=3TeV is comparable to the current experimental limits with L=1000(500) fb~(-1). If the integrated luminosity can be increased to 3000 fb~(-1), the top partner mass+mTcan be excluded up to 1350(1440) GeV at 2σ level. We also considered the initial state radiation effect, and find that this effect reduces the excluding ability of the eγ collision on the the top partner mass by approximately 10 GeV. Moreover, the ability to exclude the LHT parameter space at eγ collision complements the existing research.     

Synthesis of tetrafluorinated tetrahydroquinolines via photoredox catalysis

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