Laser imaging system for determination of three-dimensional scalar gradients in turbulent flames

2004 ◽  
Vol 29 (4) ◽  
pp. 355 ◽  
Author(s):  
Adonios N. Karpetis ◽  
Thomas B. Settersten ◽  
Robert W. Schefer ◽  
Robert S. Barlow
2018 ◽  
Vol 89 (6) ◽  
pp. 063108
Author(s):  
Wenze Xia ◽  
Yayun Ma ◽  
Shaokun Han ◽  
Yulin Wang ◽  
Fei Liu ◽  
...  

KYAMC Journal ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 48-52
Author(s):  
Mushtaq Ahmad ◽  
Md Zubaidur Rahman ◽  
Farial Naima Rahman

Virtopsy is a virtual alternative to a traditional autopsy, conducted with scanning and imaging technology. In developed countries Computed Tomography (CT) and Magnetic Resonance Imaging (MRI) are now being evaluated as complementary means for determination of cause of death. This paper explores the latest development and implication of virtopsy from ethical, clinical and technical point of view. Published literature in different journals with strict inclusion and exclusion criteria were extensively reviewed through use of general and Meta search engines to elucidate the applications and implications of virtual autopsy. The modern high-resolution imaging has been used as a well described aid in the setting of post-mortem investigations. Virtopsy introduces a new era in autopsy examination. It utilizes the technological innovation of modern imaging system to obtain best results and three Dimensional (3D) images of the body in multiple plains without mutilation of the human body. Now a days virtopsy is very much acceptable procedure to the forensic society. In western worlds virtopsy is likely to replace conventional autopsies in future. We can also try to implement this modern system in our country. KYAMC Journal.2021;12(1): 48-52


2017 ◽  
Vol 56 (3) ◽  
pp. 487 ◽  
Author(s):  
Wenze Xia ◽  
Shaokun Han ◽  
Naeem Ullah ◽  
Jingya Cao ◽  
Liang Wang ◽  
...  

Photonics ◽  
2021 ◽  
Vol 8 (6) ◽  
pp. 173
Author(s):  
Ao Yang ◽  
Jie Cao ◽  
Yang Cheng ◽  
Chuanxun Chen ◽  
Qun Hao

Traditional lidar scans the target with a fixed-size scanning spot and scanning trajectory. Therefore, it can only obtain the depth image with the same pixels as the number of scanning points. In order to obtain a high-resolution depth image with a few scanning points, we propose a scanning and depth image reconstruction method with a variable scanning spot and scanning trajectory. Based on the range information and the proportion of the area of each target (PAET) contained in the multi echoes, the region with multi echoes (RME) is selected and a new scanning trajectory and smaller scanning spot are used to obtain a finer depth image. According to the range and PAET obtained by scanning, the RME is segmented and filled to realize the super-resolution reconstruction of the depth image. By using this method, the experiments of two overlapped plates in space are carried out. By scanning the target with only forty-three points, the super-resolution depth image of the target with 160 × 160 pixels is obtained. Compared with the real depth image of the target, the accuracy of area representation (AOAR) and structural similarity (SSIM) of the reconstructed depth image is 99.89% and 98.94%, respectively. The method proposed in this paper can effectively reduce the number of scanning points and improve the scanning efficiency of the three-dimensional laser imaging system.


1996 ◽  
Vol 17 (2) ◽  
pp. 71-79 ◽  
Author(s):  
Philip V Patete ◽  
Jeffrey P Bulgrin ◽  
Mohammad M Shabani ◽  
Daniel J Smith

Author(s):  
R. Brian Smith ◽  
Bill Rogers ◽  
Gleb P. Tolstykh ◽  
Nicolas E. Walsh ◽  
Merritt G. Davis ◽  
...  

Author(s):  
M. Boublik ◽  
W. Hellmann ◽  
F. Jenkins

The present knowledge of the three-dimensional structure of ribosomes is far too limited to enable a complete understanding of the various roles which ribosomes play in protein biosynthesis. The spatial arrangement of proteins and ribonuclec acids in ribosomes can be analysed in many ways. Determination of binding sites for individual proteins on ribonuclec acid and locations of the mutual positions of proteins on the ribosome using labeling with fluorescent dyes, cross-linking reagents, neutron-diffraction or antibodies against ribosomal proteins seem to be most successful approaches. Structure and function of ribosomes can be correlated be depleting the complete ribosomes of some proteins to the functionally inactive core and by subsequent partial reconstitution in order to regain active ribosomal particles.


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