cylindrical projection
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2022 ◽  
Vol 2022 ◽  
pp. 1-9
Author(s):  
Yajun Pang

Panorama can reflect the image seen at any angle of view at a certain point of view. How to improve the quality of panorama stitching and use it as a data foundation in the “smart tourism” system has become a research hotspot in recent years. Image stitching means to use the overlapping area between the images to be stitched for registration and fusion to generate a new image with a wider viewing angle. This article takes the production of “Tai Chi” animation as an example to apply image stitching technology to the production of realistic 3D model textures to simplify the production of animation textures. A handheld camera is used to collect images in a certain overlapping area. After cylindrical projection, the Harris algorithm based on scale space is adopted to detect image feature points, the two-way normalized cross-correlation algorithm matches the feature points, and the algorithm to extract the threshold T iteratively removes mismatches. The transformation parameter model is quickly estimated through the improved RANSAC algorithm, and the spliced image is projected and transformed. The Szeliski grayscale fusion method directly calculates the grayscale average of the matching points to fuse the image, and finally, the best stitching method is used to eliminate the ghosting at the image mosaic. Data experiments based on Matlab show that the proposed image splicing technology has the advantages of high efficiency and clear spliced images and a more satisfactory panoramic image visual effect can be achieved.


2021 ◽  
Vol 3 ◽  
pp. 25-40
Author(s):  
Andrzej Kwinta ◽  
◽  
Joanna Bac-Bronowicz ◽  

This paper undertakes the problem of mapping a hyperboloid cooling tower on a single plane. Measurements performed by ground-based laser scanning technology quickly deliver substantial amounts of geometric data of the tower’s outer wall. The essence of the article is projection of the rotational hyperboloid on a plane. The shape of the hyperboloid cooling tower is not directly expandable to a single plane. Mapping a hyperboloid shape on a plane is, therefore, associated with distortions. This paper presents a comparison between cylindrical and conic projection of a hyperboloid cooling tower. The most popular method of mapping hyperboloid is cylindrical projection. The cylinder’s side surface is easily developed on the drawing sheet. For the hyperboloid cooling tower, the biggest distortions occur in the latitudinal direction and reach the highest values at the top and bottom edges. The equation (13) describe distortion for the cylindrical projection. The equation (18) describe distortion for the conical projection. This paper presents results obtained from the performed measurement. The analysis found that cone mapping produces less distortion than cylindrical projection for the hyperboloid cooling tower. We think, that in conical projection, the shape of a hyperboloid cooling tower and theoretical conic shape have better corresponding together than in cylindrical projection.


2020 ◽  
Vol 499 (1) ◽  
pp. L62-L66
Author(s):  
G Filacchione ◽  
M Ciarniello ◽  
E D’Aversa ◽  
F Capaccioni ◽  
P Cerroni ◽  
...  

ABSTRACT Photometric correction based on the Shkuratov method is applied to derive visible and infrared albedo maps of Rhea from disc-resolved Cassini VIMS data. Differently from I/F images, albedo maps offer an optimal disentanglement of composition and physical properties of the surface from illumination-viewing effects and to study spectral variations occurring at hemispherical and local scales. A similar methodology has been already applied to Dione’s and Tethys’s data sets returned by VIMS. Following the same scheme also for Rhea, spectral albedo is derived at 59 wavelengths between 0.35 and 5.047 µm. Equigonal albedo maps are rendered in cylindrical projection with a 0.5$^\circ \, \times$ 0.5° angular resolution in latitude and longitude, corresponding to a maximum spatial resolution of 6.7 km bin−1. Apart from albedo, 0.35–0.55 and 0.55–0.95 µm spectral slopes and the water ice 1.5–2.0 µm band depth maps are computed from photometric-corrected data with the specific scope to investigate the leading-trailing hemisphere colour-albedo dichotomy and to constrain spectral properties above different morphological units including fresh craters (Inktomi) and bright tectonics features (Wakonda-Avaiki Chasmata).


2019 ◽  
Author(s):  
Paul D. Caccamo ◽  
Maxime Jacq ◽  
Michael S. VanNieuwenhze ◽  
Yves V. Brun

SummaryBacteria come in an array of shapes and sizes, but the mechanisms underlying diverse morphologies are poorly understood. The peptidoglycan (PG) cell wall is the primary determinant of cell shape. At the molecular level, morphological variation often results from the regulation of enzymes involved in cell elongation and division. These enzymes are spatially controlled by cytoskeletal scaffolding proteins, that both recruit and organize the PG synthesis complex. How then do cells define alternative morphogenic processes that are distinct from cell elongation and division? To address this, we have turned to the specific morphotype of Alphaproteobacterial stalks. Stalk synthesis is a specialized form of zonal growth, which requires PG synthesis in a spatially constrained zone to extend a thin cylindrical projection of the cell envelope. The morphogen SpmX defines the site of stalk PG synthesis, but SpmX is a PG hydrolase. How then does a non-cytoskeletal protein, SpmX, define and constrain PG synthesis to form stalks? Here we report that SpmX and the bactofilin BacA act in concert to regulate stalk synthesis in Asticcacaulis biprosthecum. We show that SpmX recruits BacA to the site of stalk synthesis. BacA then serves as a stalk-specific topological organizer for PG synthesis activity, including its recruiter SpmX, at the base of the stalk. In the absence of BacA, cells produce “pseudostalks” that are the result of unconstrained PG synthesis. Therefore, the protein responsible for recruitment of a morphogenic PG remodeling complex, SpmX, is distinct from the protein that topologically organizes the complex, BacA.


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