For replicative objects images are also boarded the following features:
From frame to frame replica appear and disappear. For example, in Figure 5: Third frame - the replica has, 4th - disappeared; 11th frame - replicas have, 12th - disappeared. The same on the 13rd and 14th frames. There are replicas of the perforations and lighting illumination " (4th frame). There are replica image transitions inter-picture space and even to neighboring frames: 13-it 14-D and 23 of its 24.
You can give the following preliminary explanation of those facts. The observed phenomenon of transition image from one frame to another and exposing photographic film in the perforation can be explained by selective wavelength selection from a wide spectrum of Planar waveguides. They are formed between the upper and lower boundaries of the section thickness of fotosloâ, as well as between the substrate and film emulsion. If there are multiple reflections and scattering in the Planar waveguides with low-quality šerohovatostâh, as well as the absence in them of focusing and blending creeping "reflected image from opposite edges of film on each other, is the reciprocal of the overlay blur. Film perforations images do not lose their clarity through the relative hole krupnomasštabnosti. Power can be understood as the insufficiency of sizes of holes perforating the grain size and the emulsion. Large and high-contrast objects do not require broadcast images focusing on small distances are commensurate with the size of the image. This is due to set regarding large-scale images of light diodes in inter-picture space.
Effect of irregular registration of replication from frame to frame can be understood as: is relatively long Uv-pumping fibers of DNA with its further ionosphere re-radiation after receiving limit stored energy. Its radiation for some, but much less time. If the registration times and ejection time stored energy pumping is the replica of the registration permit DNA and surrounding objects, and if these times-going registration replicas. When an optimal time step registration, coinciding with the interim step otstrelivaemoj energy pumping laser waveguides DNA, registration will be continuously reproduced from one frame to the next.
Previously we have postulated, that DNA in vivo-in vitro is a hologram-forming medium [8,9]. By adopting this, You can believe, the photosensitive medium DNA, as the collagen (gelatin), can be artificially recorded hologram in the blue and ultraviolet spectra. In such a case when we used blue and ultraviolet irradiation lamps is the simultaneous preparation of DNA on the Auto record himself and parallel entry nearest surrounding objects on photosensitive kvazicilindričeskie DNA able hard gel. Then each of them red and infrared- radiation is read many diffraction image of distorted and blurry bright first and, the weaker, all subsequent orders of diffraction images, the displaced relative to each other. This registration of holograms in the ultraviolet and then in the red and INFRARED- range leads to blurring of the image. This blurring occurs both because of their multiple spatial diversity images, and at the expense of several orders of magnitude from each strand of DNA fibers. Blur also occurs at the expense of its own DNA drug acoustic vibrations with the effect of Fermi-Pasta-Ulam [8].
It seems to us, that such replicating images at higher doses of ultraviolet radiation, for example with sunburn, in the skin layers and adjacent tissue of humans can cause abnormal program holographic control when reading a false red and infrared- ranges of sunlight. This, in turn,, When a certain brightness level threshold later reconstructed holographic images, can lead to certain types of malignant tumors. For melanoma is already known.
In addition to registering the holograms because of high energy ultraviolet radiation at the time of registration for the holograms is the effect of a partial extract electrons and partial violation of DNA structures, which leads to an accumulation of free, type of capacitor charge on the surface of DNA fibers. The accumulated charge creates an effect of spatial redistribution of fibers, that, in turn,, affects the priority distribution of reconstructed images. Image offset, reduced diffraction orders, in the direction opposite to the initial diffraction due to the condenser effect change of charge sign-minus to plus and back. In contact with such space-distributed kvazikondensatorom through partial diversion and reallocation of charges and their relative positions of detected a new effect with the emergence of right-wing or left-wing orders of diffraction in managed DNA nanostructures. This effect is observed in Figure 5 ((a), b). This effect can then be used to create managed spatial DNA nanostructures, for example, in the processes of regeneration of organs and tissues of people through targeted holographic control, the primary form is received [21, 22].
We must emphasize the, the detected effects education DNA replica of the wave and the environment need more accurate experimental production and theoretical justification. Very much in this part is unclear and therefore research continues.
