By choosing a PVC slice to simulate flexible vegetation, we carried out experiments in an open channel with submerged flexible vegetation. A 3D acoustic Doppler velocimeter （micro ADV） was used to measure local flow...By choosing a PVC slice to simulate flexible vegetation, we carried out experiments in an open channel with submerged flexible vegetation. A 3D acoustic Doppler velocimeter （micro ADV） was used to measure local flow velocities and Reynolds stress. The results show that hydraulic characteristics in non-vegetation and vegetation layers are totally different. In a region above the vegetation, Reynolds stress distribution is linear, and the measured velocity profile is a classical logarithmic one. Based on the concept of new-riverbed, the river compression parameter representing the impact of vegetation on river is given, and a new assumption of mixing length expression is made. The formula for time-averaged velocity derived from the expression requires less parameters and simple calculation, and is useful in applications.展开更多
Kernel size, one of the traits that determine wheat yield, is controlled by multiple quantitative trait loci.Polish wheat(Triticum polonicum) has elongated and plump kernel and is a valuable material for breeding high...Kernel size, one of the traits that determine wheat yield, is controlled by multiple quantitative trait loci.Polish wheat(Triticum polonicum) has elongated and plump kernel and is a valuable material for breeding high-yielding wheat cultivars. However, genes or loci determining kernel length(KL) in Polish wheat are unknown. We identified and validated a major KL gene, KL-PW, at the P1 locus in Polish wheat. KL-PW is VRT-A2, which encodes a MIKC-type MADS-box protein(MADS55). An insertion/deletion mutation in intron 1 of VRT-A2;led to an alternatively spliced transcript, VRT-A2;. Quantitative PCR analysis showed that VRT-A2;was more highly expressed in developing seeds than was VRT-A2 Ailanmai.Brassinosteroid(BR) sensitivity experiment and the expression of BR-related genes indicated that VRTA2;functions as a positive regulator of BR responses. VRT-A2;significantly increased KL of wheat.These findings not only reveal the molecular basis of KL-PW in controlling KL, but also provide a valuable genetic resource for increasing kernel size in wheat.展开更多
This study intends to find out the correlation between the cover depth and the bond characteristics of UHPC through pull-out tests of UHPC specimens with different cover depths and bond tests of rebar using flexural m...This study intends to find out the correlation between the cover depth and the bond characteristics of UHPC through pull-out tests of UHPC specimens with different cover depths and bond tests of rebar using flexural members. In this experimental study, specimens are fabricated with the lap-splice length as test variable in relation with the calculation of the lap-splice length for 180- MPa UHPC. Moreover, specimens are also fabricated with the cover depth as test variable to evaluate the effect of the cover depth on the UHPC flexural members. The load-displacement curves are analyzed for each of these test variables to compute the lap-splice length proposed in the K-UHPC structural design guideline and to evaluate the influence of the cover depth on the flexural members. As a result, the stability of the structural behavior can be significantly enhanced by increasing slightly the cover depth specification of the current UHPC Structure Design Guideline from the maximum value between 1.5 times of rebar diameter and 20 mm to the maximum value between 1.5 times of rebar diameter and 25 mm.展开更多
With the growth of the Internet,more and more business is being done online,for example,online offices,online education and so on.While this makes people’s lives more convenient,it also increases the risk of the netw...With the growth of the Internet,more and more business is being done online,for example,online offices,online education and so on.While this makes people’s lives more convenient,it also increases the risk of the network being attacked by malicious code.Therefore,it is important to identify malicious codes on computer systems efficiently.However,most of the existing malicious code detection methods have two problems:(1)The ability of the model to extract features is weak,resulting in poor model performance.(2)The large scale of model data leads to difficulties deploying on devices with limited resources.Therefore,this paper proposes a lightweight malicious code identification model Lightweight Malicious Code Classification Method Based on Improved SqueezeNet(LCMISNet).In this paper,the MFire lightweight feature extraction module is constructed by proposing a feature slicing module and a multi-size depthwise separable convolution module.The feature slicing module reduces the number of parameters by grouping features.The multi-size depthwise separable convolution module reduces the number of parameters and enhances the feature extraction capability by replacing the standard convolution with depthwise separable convolution with different convolution kernel sizes.In addition,this paper also proposes a feature splicing module to connect the MFire lightweight feature extraction module based on the feature reuse and constructs the lightweight model LCMISNet.The malicious code recognition accuracy of LCMISNet on the BIG 2015 dataset and the Malimg dataset reaches 98.90% and 99.58%,respectively.It proves that LCMISNet has a powerful malicious code recognition performance.In addition,compared with other network models,LCMISNet has better performance,and a lower number of parameters and computations.展开更多
Through analysis of EST database, a 1,226bp cDNA assembled from 8 ESTs with significant similarity to human spinocerebellar ataxia2 gene(ataxin2) is found. Based on these sequences, a 4,657bp complete coding cDNA whic...Through analysis of EST database, a 1,226bp cDNA assembled from 8 ESTs with significant similarity to human spinocerebellar ataxia2 gene(ataxin2) is found. Based on these sequences, a 4,657bp complete coding cDNA which is predicated to encode 1,052 amino acids is cloned, which is termed ataxin 2 like. Northern blot analysis indicates that human ataxin2 like has two splicing forms. Comparison analysis between human ataxin2 and ataxin2 like shows that both cDNA and the protein predicated share striking similarity. Structure analysis of the protein indicates that it is a strongly hydrophilic protein. The gene is further mapped to chromosome 9p 11 by fluoresence in situ hybridization.展开更多
基金supported by the National Natural Science Foundation of China (Nos. 50679061, 50709025,50749031)
文摘By choosing a PVC slice to simulate flexible vegetation, we carried out experiments in an open channel with submerged flexible vegetation. A 3D acoustic Doppler velocimeter （micro ADV） was used to measure local flow velocities and Reynolds stress. The results show that hydraulic characteristics in non-vegetation and vegetation layers are totally different. In a region above the vegetation, Reynolds stress distribution is linear, and the measured velocity profile is a classical logarithmic one. Based on the concept of new-riverbed, the river compression parameter representing the impact of vegetation on river is given, and a new assumption of mixing length expression is made. The formula for time-averaged velocity derived from the expression requires less parameters and simple calculation, and is useful in applications.
基金supported by the National Natural Science Foundation of China(31671688)the Bureau of Science and Technology of Sichuan Province(2020YJ0141)。
文摘Kernel size, one of the traits that determine wheat yield, is controlled by multiple quantitative trait loci.Polish wheat(Triticum polonicum) has elongated and plump kernel and is a valuable material for breeding high-yielding wheat cultivars. However, genes or loci determining kernel length(KL) in Polish wheat are unknown. We identified and validated a major KL gene, KL-PW, at the P1 locus in Polish wheat. KL-PW is VRT-A2, which encodes a MIKC-type MADS-box protein(MADS55). An insertion/deletion mutation in intron 1 of VRT-A2;led to an alternatively spliced transcript, VRT-A2;. Quantitative PCR analysis showed that VRT-A2;was more highly expressed in developing seeds than was VRT-A2 Ailanmai.Brassinosteroid(BR) sensitivity experiment and the expression of BR-related genes indicated that VRTA2;functions as a positive regulator of BR responses. VRT-A2;significantly increased KL of wheat.These findings not only reveal the molecular basis of KL-PW in controlling KL, but also provide a valuable genetic resource for increasing kernel size in wheat.
文摘This study intends to find out the correlation between the cover depth and the bond characteristics of UHPC through pull-out tests of UHPC specimens with different cover depths and bond tests of rebar using flexural members. In this experimental study, specimens are fabricated with the lap-splice length as test variable in relation with the calculation of the lap-splice length for 180- MPa UHPC. Moreover, specimens are also fabricated with the cover depth as test variable to evaluate the effect of the cover depth on the UHPC flexural members. The load-displacement curves are analyzed for each of these test variables to compute the lap-splice length proposed in the K-UHPC structural design guideline and to evaluate the influence of the cover depth on the flexural members. As a result, the stability of the structural behavior can be significantly enhanced by increasing slightly the cover depth specification of the current UHPC Structure Design Guideline from the maximum value between 1.5 times of rebar diameter and 20 mm to the maximum value between 1.5 times of rebar diameter and 25 mm.
文摘With the growth of the Internet,more and more business is being done online,for example,online offices,online education and so on.While this makes people’s lives more convenient,it also increases the risk of the network being attacked by malicious code.Therefore,it is important to identify malicious codes on computer systems efficiently.However,most of the existing malicious code detection methods have two problems:(1)The ability of the model to extract features is weak,resulting in poor model performance.(2)The large scale of model data leads to difficulties deploying on devices with limited resources.Therefore,this paper proposes a lightweight malicious code identification model Lightweight Malicious Code Classification Method Based on Improved SqueezeNet(LCMISNet).In this paper,the MFire lightweight feature extraction module is constructed by proposing a feature slicing module and a multi-size depthwise separable convolution module.The feature slicing module reduces the number of parameters by grouping features.The multi-size depthwise separable convolution module reduces the number of parameters and enhances the feature extraction capability by replacing the standard convolution with depthwise separable convolution with different convolution kernel sizes.In addition,this paper also proposes a feature splicing module to connect the MFire lightweight feature extraction module based on the feature reuse and constructs the lightweight model LCMISNet.The malicious code recognition accuracy of LCMISNet on the BIG 2015 dataset and the Malimg dataset reaches 98.90% and 99.58%,respectively.It proves that LCMISNet has a powerful malicious code recognition performance.In addition,compared with other network models,LCMISNet has better performance,and a lower number of parameters and computations.
文摘Through analysis of EST database, a 1,226bp cDNA assembled from 8 ESTs with significant similarity to human spinocerebellar ataxia2 gene(ataxin2) is found. Based on these sequences, a 4,657bp complete coding cDNA which is predicated to encode 1,052 amino acids is cloned, which is termed ataxin 2 like. Northern blot analysis indicates that human ataxin2 like has two splicing forms. Comparison analysis between human ataxin2 and ataxin2 like shows that both cDNA and the protein predicated share striking similarity. Structure analysis of the protein indicates that it is a strongly hydrophilic protein. The gene is further mapped to chromosome 9p 11 by fluoresence in situ hybridization.
