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Image inner circles

This example shows the round particle in cell B,B with two possible nonbonded cutoffs. With the outer cutoff, the round particle interacts with both the rectangle and its periodic image. By reducing the nonbonded cutoff to an appropriate radius (the inner circle), the round particle can interact with only one rectangle—in this case, the rectangle also in cell B,B. ... [Pg.64]

Figure 14.12 Relative Lorentz factor. The image depicts a perpendicular section of a capillary of diameter L being illuminated by a beam of width W. Only crystallites falling in the light grey inner circle are rotated completely (27t) within the beam. Crystallites outside this region but still within the beam path only experience a limited rotation co, thus reducing the effective single crystal Lorentz factor to be applied to them. Figure 14.12 Relative Lorentz factor. The image depicts a perpendicular section of a capillary of diameter L being illuminated by a beam of width W. Only crystallites falling in the light grey inner circle are rotated completely (27t) within the beam. Crystallites outside this region but still within the beam path only experience a limited rotation co, thus reducing the effective single crystal Lorentz factor to be applied to them.
Figure 14.2 Phase contrast microscopic images of conditionally immortalized cells forming the inner blood-retinal barrier (A) and time-course of [3H] adenosine uptake by TR-iBRB cells (B). A Conditionally immortalized rat retinal capillary endothelial cell line TR-iBRB, retinal pericyte cell line TR-rPCT and Muller cell line TR-MUL. B The [ H]adenosine (14 nM) uptake was performed at 37°C in the presence (closed circle) or absence (open circle) of Na+. Figure 14.2 Phase contrast microscopic images of conditionally immortalized cells forming the inner blood-retinal barrier (A) and time-course of [3H] adenosine uptake by TR-iBRB cells (B). A Conditionally immortalized rat retinal capillary endothelial cell line TR-iBRB, retinal pericyte cell line TR-rPCT and Muller cell line TR-MUL. B The [ H]adenosine (14 nM) uptake was performed at 37°C in the presence (closed circle) or absence (open circle) of Na+.
Camera raw image contains the iris and its surroundings. Thus, the iris localization methods must be applied to extract the valuable iris texture information available within the image. Localization of both inner (i.e., between the pupil and the iris) and outer (i.e., between the iris and the sclera) iris boundaries makes use of local image gradient estimation. Consequently, we approximate the shape of inner and outer boundaries by two non-concentric circles. Figure 2 presents the camera raw image with iris both circular boundaries localized. [Pg.261]

Figure 3 shows video images of fiber growth made through a window at the top of the growth tube each dark circle defines the inner wall of the tube at a different time. Figure 3a was made after the growth tube had been exposed to the experimental conditions cited above for 9.5 h. Very thin fibers first became visible within 30 minutes (Figure 3b). These fibers continued to thicken with time and thus became more visible as the experiment was concluded. Figure 3 shows video images of fiber growth made through a window at the top of the growth tube each dark circle defines the inner wall of the tube at a different time. Figure 3a was made after the growth tube had been exposed to the experimental conditions cited above for 9.5 h. Very thin fibers first became visible within 30 minutes (Figure 3b). These fibers continued to thicken with time and thus became more visible as the experiment was concluded.
Figure 13-8. SEM images of the tunic cords in P. misakiensis after treatment with UpdegrafF reagent, (a) Numerous tunic cords in random arrays are located on the inner surface of dorsal tunic, (b) A magnified image of a siphon, highlighted by a circle in (a). Tunic cords are often connected to the rim of the internal tunic just like an eyelet structure. Most of the tunic cords are coiled (c) and the apical end is observed as a swollen and ornamented structure (d). (Figures 11,5, and 7 from Kimura, S. and Itoh, T. 1998. A new cellulosic structure, the timic cord in the ascidian Polyandrocarpa misakiensis. Protoplasma 204 94-102. Reproduced with kind permission of Springer Science and Business Media). Figure 13-8. SEM images of the tunic cords in P. misakiensis after treatment with UpdegrafF reagent, (a) Numerous tunic cords in random arrays are located on the inner surface of dorsal tunic, (b) A magnified image of a siphon, highlighted by a circle in (a). Tunic cords are often connected to the rim of the internal tunic just like an eyelet structure. Most of the tunic cords are coiled (c) and the apical end is observed as a swollen and ornamented structure (d). (Figures 11,5, and 7 from Kimura, S. and Itoh, T. 1998. A new cellulosic structure, the timic cord in the ascidian Polyandrocarpa misakiensis. Protoplasma 204 94-102. Reproduced with kind permission of Springer Science and Business Media).
FIGURE 4.3 Examples of in situ HRTEM images of CNTs at 1360°C. (a) SWNT with a diameter of 0.8 mn, near the size of a fullerene Cgo, 0.7 nm, (b) SWNT with a diameter of 1.5 mn, (e) DWNT, and (d) DWNT shaped like a water drop. An inner ring in concentric circles has a weak intensity compared to the outer ring. It is suggested that the inner ring forms after the formation of the outer ring. (From Watanabe, H. et al.. Journal... [Pg.118]


See other pages where Image inner circles is mentioned: [Pg.64]    [Pg.143]    [Pg.52]    [Pg.168]    [Pg.1709]    [Pg.91]    [Pg.5]    [Pg.58]    [Pg.232]    [Pg.377]    [Pg.3198]    [Pg.31]    [Pg.50]    [Pg.1709]    [Pg.340]    [Pg.749]    [Pg.147]    [Pg.203]   
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