scholarly journals The optics of the human eye at 8.6 μm lateral resolution

Author(s):  
Sergio Bonaque-Gonzalez ◽  
Juan M. Trujillo-Sevilla ◽  
Miriam Velasco-Ocana ◽  
Oscar Casanova-Gonzalez ◽  
Miguel Sicilia-Cabrera ◽  
...  

Ocular optics is normally estimated based on 2,600 measurement points within the pupil of the eye, which implies a lateral resolution of approximately 175 microns for a 9 mm pupil diameter. This is because information below this resolution is not thought to be relevant or even possible to obtain with current measurement systems. In this work, we characterize the in vivo ocular optics of the human eye with a lateral resolution of 8.6 microns, which implies roughly 1 million measurement points for a pupil diameter of 9 mm. The results suggest that the normal human eye presents a series of hitherto unknown optical patterns with amplitudes between 200 and 300 nm and is made up of a series of in-phase peaks and valleys. If the results are analysed at only high lateral frequencies, the human eye is also found to contain a whole range of new information. This discovery could have a great impact on the way we understand some fundamental mechanisms of human vision and could be of outstanding utility in certain fields of ophthalmology.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Sergio Bonaque-González ◽  
Juan M. Trujillo-Sevilla ◽  
Miriam Velasco-Ocaña ◽  
Óscar Casanova-González ◽  
Miguel Sicilia-Cabrera ◽  
...  

AbstractOcular optics is normally estimated based on up to 2,600 measurement points within the pupil of the eye, which implies a lateral resolution of approximately 175 µm for a 9 mm pupil diameter. This is because information below this resolution is not thought to be relevant or even possible to obtain with current measurement systems. In this work, we characterize the in vivo ocular optics of the human eye with a lateral resolution of 8.6 µm, which implies roughly 1 million measurement points for a pupil diameter of 9 mm. The results suggest that the normal human eye presents a series of hitherto unknown optical patterns with amplitudes between 200 and 300 nm and is made up of a series of in-phase peaks and valleys. If the results are analysed at only high lateral frequencies, the human eye is also found to contain a whole range of new information. This discovery could have a great impact on the way we understand some fundamental mechanisms of human vision and could be of outstanding utility in certain fields of ophthalmology.


Author(s):  
Karen Neander

In the second chapter, the author describes some research by cognitive scientists, who posit nonconceptual representations to explain certain perceptual capacities (and incapacities). This research and the way in which it is reported illustrate the type of theoretical work done by an error-permitting notion of nonconceptual representation, alongside a malfunction-permitting notion of function. One set of studies (led by McCloskey) that is described in some detail focuses on an unusual deficit in locating visual targets (in a young woman, AH), which were intended to contribute to understanding normal human vision. The author makes clear why the contents ascribed to the underlying representational states, where the errors first occur, are referential-intentional contents, not merely (natural-factive) informational contents, and why their ascriptions count as intensional, according to standard criteria. Toward the end of the chapter, the author reminds readers of a familiar conundrum: if a representation’s having content is not causally potent in a psychological process, why is it (still) a central tenet of mainstream cognitive science that such a process should be understood as representational?


1994 ◽  
Vol 2 (8) ◽  
pp. 3-4
Author(s):  
Barry D. Masters

The living human eye is in constant motion. The cornea, which is the transparent front surface of the eyeball, is a formidable specimen for microscopy. How can we use a microscope to obtain sufficient contrast in order to observe cellular and subcellular details on a moving, transparent specimen? Although the normal human cornea is free of blood vessels, there are many nerves within the 500 μm thickness of this tissue. How can we observe these nerves in the living human eye?To accomplish these aims, use a new real-time, scanning slit confocal microscope that was developed by Dr. A. Thaer for imaging the in vivo human cornea. The optical design of the real-time, scanning slit confocal microscope is shown as follows in Figure 1. The confocal microscope is a modification of the real-time, scanning slit confocal microscope based on an oscillating too-sided mirror (bi-lateral scanning) which was designed and first constructed in 1969 by G. M. Svishchev in Lenningrad.


Author(s):  
N. P. Dmitrieva

One of the most characteristic features of cancer cells is their ability to metastasia. It is suggested that the modifications of the structure and properties of cancer cells surfaces play the main role in this process. The present work was aimed at finding out what ultrastructural features apear in tumor in vivo which removal of individual cancer cells from the cell population can provide. For this purpose the cellular interactions in the normal human thyroid and cancer tumor of this gland electron microscopic were studied. The tissues were fixed in osmium tetroxide and were embedded in Araldite-Epon.In normal human thyroid the most common type of intercellular contacts was represented by simple junction formed by the parallelalignment of adjacent cell membranees leaving in between an intermembranes space 15-20 nm filled with electronlucid material (Fig. 1a). Sometimes in the basal part of cells dilatations of the intercellular space 40-50 nm wide were found (Fig. 1a). Here the cell surfaces may form single short microvilli.


1992 ◽  
Vol 67 (01) ◽  
pp. 060-062 ◽  
Author(s):  
J Harsfalvi ◽  
E Tarcsa ◽  
M Udvardy ◽  
G Zajka ◽  
T Szarvas ◽  
...  

Summaryɛ(γ-glutamyl)lysine isodipeptide has been detected in normal human plasma by a sensitive HPLC technique in a concentration of 1.9-3.6 μmol/1. Incubation of in vitro clotted plasma at 37° C for 12 h resulted in an increased amount of isodipeptide, and there was no further significant change when streptokinase was also present. Increased in vivo isodipeptide concentrations were also observed in hypercoagulable states and during fibrinolytic therapy.


Author(s):  
Marlien van Mever ◽  
Karen Segers ◽  
Debby Mangelings ◽  
Thomas Hankemeier ◽  
Yvan Vander Heyden ◽  
...  
Keyword(s):  

Author(s):  
Sabina Pozzi ◽  
Anna Scomparin ◽  
Sahar Israeli-Dangoor ◽  
Daniel Rodriguez ◽  
Paula Ofek ◽  
...  
Keyword(s):  

Author(s):  
Shu-Chieh Hu ◽  
Matthew S Bryant ◽  
Estatira Sepehr ◽  
Hyun-Ki Kang ◽  
Raul Trbojevich ◽  
...  

Abstract The tobacco-specific nitrosamine NNK [4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone] is found in tobacco products and tobacco smoke. NNK is a potent genotoxin and human lung carcinogen; however, there are limited inhalation data for the toxicokinetics (TK) and genotoxicity of NNK in vivo. In the present study, a single dose of 5x10−5, 5x10−3, 0.1, or 50 mg/kg body weight (BW) of NNK, 75% propylene glycol (vehicle control), or air (sham control) was administered to male Sprague-Dawley (SD) rats (9-10 weeks age) via nose-only inhalation (INH) exposure for 1 hour. For comparison, the same doses of NNK were administered to male SD rats via intraperitoneal (IP) injection and oral gavage (PO). Plasma, urine, and tissue specimens were collected at designated timepoints and analyzed for levels of NNK and its major metabolite 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) and tissue levels of DNA adduct O6-methylguanine by LC/MS/MS. TK data analysis was performed using a non-linear regression program. For the genotoxicity subgroup, tissues were collected at 3 hours post-dosing for comet assay analysis. Overall, the TK data indicated that NNK was rapidly absorbed and metabolized extensively to NNAL after NNK administration via the three routes. The IP route had the greatest systemic exposure to NNK. NNK metabolism to NNAL appeared to be more efficient via INH than IP or PO. NNK induced significant increases in DNA damage in multiple tissues via the three routes. The results of this study provide new information and understanding of the toxicokinetics and genotoxicity of NNK.


Blood ◽  
1992 ◽  
Vol 80 (5) ◽  
pp. 1190-1198 ◽  
Author(s):  
SC Guba ◽  
CI Sartor ◽  
LR Gottschalk ◽  
YH Jing ◽  
T Mulligan ◽  
...  

Abstract Bone marrow (BM) stromal fibroblasts produce hematopoietic growth factors (HGFs) in response to inflammatory mediators such as tumor necrosis factor-alpha or interleukin-1 alpha (IL-1 alpha). In the absence of such inflammatory stimuli, production of HGFs by BM stromal cells has been problematic and controversial. In vivo, however, basal hematopoiesis maintains blood counts within a normal homeostatic range even in the absence of inflammation, and HGFs are required for progenitor cell differentiation in vitro. To better ascertain the contribution of BM stromal fibroblasts to basal hematopoiesis, we therefore studied HGF production in quiescent BM stromal fibroblasts by three sensitive assays: serum-free bioassay, enzyme-linked immunosorbent assay, and reverse transcriptase polymerase chain reaction. Stromal fibroblasts were cultured in the presence or absence of normal human serum to determine if serum factor(s) present in the noninflammatory (basal) state induce secretion of HGFs. Human serum was found to induce or enhance transcription and secretion of granulocyte- macrophage colony-stimulating factor (GM-CSF) and enhance secretion of constitutively expressed IL-6. In contrast, no secretion of either granulocyte-CSF (G-CSF) or IL-3 was found. These data indicate that factors in normal human serum are active in enhancing GM-CSF and IL-6 production by stromal fibroblasts and suggest that these growth factors contribute to the maintainance of normal, basal hematopoiesis in vivo.


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