Diffraction of random light emission in a monochromatic sound wave field in an anisotropic disperising medium

1989 ◽  
Vol 32 (1) ◽  
pp. 79-89
Author(s):  
G. N. Glazov ◽  
A. S. Zadorin
Keyword(s):  
Wave Field ◽  
Sound Wave ◽  
Light Emission

scholarly journals Motion of a rigid prolate spheroid in a sound wave field

2014 ◽  
Vol 136 (2) ◽  
pp. EL179-EL184 ◽  
Author(s):  
Hongkun Zhou ◽  
Lianjin Hong
Keyword(s):  
Wave Field ◽  
Sound Wave ◽  
Prolate Spheroid

scholarly journals Insights into agglomeration and separation of fly-ash particles in a sound wave field

RSC Advances ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 5224-5233 ◽  
Author(s):  
Mengshi Lu ◽  
Mengxiang Fang ◽  
Mingchun He ◽  
Shuxin Liu ◽  
Zhongyang Luo
Keyword(s):  
Fly Ash ◽  
Wave Field ◽  
Sound Wave ◽  
High Speed ◽  
High Speed Camera ◽  
Separation Processes

A high-speed camera was used to observed the acoustic agglomeration and separation processes of fly-ash particles.

Metal-Insulator-Metal Tunneling Light-Emission Junction in Surface Acoustic Wave Field

1994 ◽  
Vol 33 (Part 2, No. 11B) ◽  
pp. L1610-L1612 ◽  
Author(s):  
Cai Yi Min ◽  
Sun Cheng Xiu ◽  
Gao Zhong Lin
Keyword(s):  
Acoustic Wave ◽  
Wave Field ◽  
Surface Acoustic Wave ◽  
Light Emission ◽  
Metal Insulator ◽  
Metal Insulator Metal

scholarly journals Numerical Study of the Movement of Fine Particle in Sound Wave Field

2015 ◽  
Vol 75 ◽  
pp. 2415-2420 ◽  
Author(s):  
Dong Zhou ◽  
Zhongyang Luo ◽  
Mengxiang Fang ◽  
Jianping Jiang ◽  
Hao Chen ◽  
...  
Keyword(s):  
Wave Field ◽  
Sound Wave ◽  
Fine Particle ◽  
Numerical Study

Renilla Bioluminescence: A Morphologic Approach to the Location of Photocytes

1974 ◽  
Vol 32 ◽  
pp. 208-209
Author(s):  
Ben O. Spurlock ◽  
Milton J. Cormier
Keyword(s):  
Excited State ◽  
Ground State ◽  
Molecular Basis ◽  
Light Emission ◽  
Chemical Basis ◽  
Electronic Excited State ◽  
Colonial Form ◽  
The Common ◽  
Eighteenth And Nineteenth Centuries ◽  
Catalyzed Oxidation

The phenomenon of bioluminescence has fascinated layman and scientist alike for many centuries. During the eighteenth and nineteenth centuries a number of observations were reported on the physiology of bioluminescence in Renilla, the common sea pansy. More recently biochemists have directed their attention to the molecular basis of luminosity in this colonial form. These studies have centered primarily on defining the chemical basis for bioluminescence and its control. It is now established that bioluminescence in Renilla arises due to the luciferase-catalyzed oxidation of luciferin. This results in the creation of a product (oxyluciferin) in an electronic excited state. The transition of oxyluciferin from its excited state to the ground state leads to light emission.

Scanning luminescence x-ray microscopy: Progress toward selective staining using microspheres

1994 ◽  
Vol 52 ◽  
pp. 74-75
Author(s):  
C. Jacobsen ◽  
J. Fu ◽  
S. Mayer ◽  
Y. Wang ◽  
S. Williams
Keyword(s):  
Visible Light ◽  
Active Sites ◽  
Light Emission ◽  
Chinese Hamster ◽  
Polystyrene Spheres ◽  
Good Resistance ◽  
X Ray ◽  
Selective Staining ◽  
Visible Light Emission ◽  
Specific Labelling

In scanning luminescence x-ray microscopy (SLXM), a high resolution x-ray probe is used to excite visible light emission (see Figs. 1 and 2). The technique has been developed with a goal of localizing dye-tagged biochemically active sites and structures at 50 nm resolution in thick, hydrated biological specimens. Following our initial efforts, Moronne et al. have begun to develop probes based on biotinylated terbium; we report here our progress towards using microspheres for tagging.Our initial experiments with microspheres were based on commercially-available carboxyl latex spheres which emitted ~ 5 visible light photons per x-ray absorbed, and which showed good resistance to bleaching under x-ray irradiation. Other work (such as that by Guo et al.) has shown that such spheres can be used for a variety of specific labelling applications. Our first efforts have been aimed at labelling ƒ actin in Chinese hamster ovarian (CHO) cells. By using a detergent/fixative protocol to load spheres into cells with permeabilized membranes and preserved morphology, we have succeeded in using commercial dye-loaded, spreptavidin-coated 0.03μm polystyrene spheres linked to biotin phalloidon to label f actin (see Fig. 3).

The Advantages of Cryotechniques: Application To Bioluminescent Cells

1990 ◽  
Vol 48 (1) ◽  
pp. 486-487
Author(s):  
Gisèle Nicolas ◽  
Jean-Marie Bassot ◽  
Marie-Thérèse Nicolas
Keyword(s):  
Endoplasmic Reticulum ◽  
Striated Muscle ◽  
Light Emission ◽  
Stable State ◽  
Freeze Substitution ◽  
Initial Step ◽  
Point Of Interest ◽  
Cell Components ◽  
Excellent Preservation ◽  
External Water

The use of fast-freeze fixation (FFF) followed by freeze-substitution (FS) brings substantial advantages which are due to the extreme rapidity of this fixation compared to the conventional one. The initial step, FFF, physically immobilizes most molecules and therefore arrests the biological reactions in a matter of milliseconds. The second step, FS, slowly removes the water content still in solid state and, at the same time, chemically fixes the other cell components in absence of external water. This procedure results in an excellent preservation of the ultrastructure, avoids osmotic artifacts,maintains in situ most soluble substances and keeps up a number of cell activities including antigenicities. Another point of interest is that the rapidity of the initial immobilization enables the capture of unstable structures which, otherwise, would slip towards a more stable state. When combined with electrophysiology, this technique arrests the ultrastructural modifications at a well defined state, allowing a precise timing of the events.We studied the epithelium of the elytra of the scale-worm, Harmothoe lunulata which has excitable, conductible and bioluminescent properties. The intracellular sites of the light emission are paracrystals of endoplasmic reticulum (PER), named photosomes (Fig.1). They are able to flash only when they are coupled with plasma membrane infoldings by dyadic or triadic junctions (Fig.2) basically similar to those of the striated muscle fibers. We have studied them before, during and after stimulation. FFF-FS showed that these complexes are labile structures able to diffentiate and dedifferentiate within milliseconds. Moreover, a transient network of endoplasmic reticulum was captured which we have named intermediate endoplasmic reticulum (IER) surrounding the PER (Fig.1). Numerous gap junctions are found in the membranous infoldings of the junctional complexes (Fig.3). When cryofractured, they cleave unusually (Fig.4-5). It is tempting to suggest that they play an important role in the conduction of the excitation.

Simulation of Sound Wave Propagation With Damping for Realistic Sound rendering for Games and Interactive Applications

2012 ◽  
Author(s):  
Bruno Moreira ◽  
Mauricio Kischinhevsky ◽  
Marcelo Zamith ◽  
Esteban Clua ◽  
Diego Brandao
Keyword(s):  
Wave Propagation ◽  
Sound Wave ◽  
Interactive Applications ◽  
Sound Rendering
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