939 resultados para goldfish, colour-blind, motion detection, trainingsexperiments, random dot pattern
Resumo:
Sensing systems in living bodies offer a large variety of possible different configurations and philosophies able to be emulated in artificial sensing systems. Motion detection is one of the areas where different animals adopt different solutions and, in most of the cases, these solutions reflect a very sophisticated form. One of them, the mammalian visual system, presents several advantages with respect to the artificial ones. The main objective of this paper is to present a system, based on this biological structure, able to detect motion, its sense and its characteristics. The configuration adopted responds to the internal structure of the mammalian retina, where just five types of cells arranged in five layers are able to differentiate a large number of characteristics of the image impinging onto it. Its main advantage is that the detection of these properties is based purely on its hardware. A simple unit, based in a previous optical logic cell employed in optical computing, is the basis for emulating the different behaviors of the biological neurons. No software is present and, in this way, no possible interference from outside affects to the final behavior. This type of structure is able to work, once the internal configuration is implemented, without any further attention. Different possibilities are present in the architecture to be presented: detection of motion, of its direction and intensity. Moreover, some other characteristics, as symmetry may be obtained.
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As it is known, there are five types of neurons in the mammalian retinal layer allowing the detection of several important characteristics of the visual image impinging onto the visual system, namely, photoreceptors, horizontal cells, amacrine, bipolar and ganglion cells. And it is a well known fact too, that the amacrine neuron architecture allows a first detection for objects motion, being the most important retinal cell to this function. We have already studied and simulated the Dowling retina model and we have verified that many complex processes in visual detection is performed with the basis of the amacrine cell synaptic connections. This work will show how this structure may be employed for motion detection
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This paper introduces a blind multiuser detection algorithm for MIMO channels. The receiver is required to separate and recover the information signal of the desired user(s) based on independent component analysis (ICA) of the received sequence. The received sequence is assumed to be independent identically distributed. Experimental results show that the proposed blind ICA multiuser detection works well with a short symbol sequence, even if the channel time span is not accurately estimated. It is concluded that the proposed blind multiuser detection performs better than the conventional matched filters in a noisy environment.
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We tested the hypothesis that the differences in performance between developmental dyslexics and controls on visual tasks are specific for the detection of dynamic stimuli. We found that dyslexics were less sensitive than controls to coherent motion in dynamic random dot displays. However, their sensitivity to control measures of static visual form coherence was not significantly different from that of controls. This dissociation of dyslexics' performance on measures that are suggested to tap the sensitivity of different extrastriate visual areas provides evidence for an impairment specific to the detection of dynamic properties of global stimuli, perhaps resulting from selective deficits in dorsal stream functions. © 2001 Lippincott Williams & Wilkins.
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One developing theme in consciousness research is that consciousness is not the product of any specific component of the brain, rather it is an emergent property of the changing patterns of connectivity between different specialised functional components. For example, the dynamic core hypothesis proposes that conscious experience requires high levels of neural complexity, where complexity is defined in terms of functional connectivity. To test this hypothesis, electroencephalography was recorded while participants were shown random dot-stereograms. Consistent with the dynamic core hypothesis, neural complexity increased as the participants changed from simply viewing the stereogram to consciously perceiving the hidden 3D image.
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Head motion during a Positron Emission Tomography (PET) brain scan can considerably degrade image quality. External motion-tracking devices have proven successful in minimizing this effect, but the associated time, maintenance, and workflow changes inhibit their widespread clinical use. List-mode PET acquisition allows for the retroactive analysis of coincidence events on any time scale throughout a scan, and therefore potentially offers a data-driven motion detection and characterization technique. An algorithm was developed to parse list-mode data, divide the full acquisition into short scan intervals, and calculate the line-of-response (LOR) midpoint average for each interval. These LOR midpoint averages, known as “radioactivity centroids,” were presumed to represent the center of the radioactivity distribution in the scanner, and it was thought that changes in this metric over time would correspond to intra-scan motion.
Several scans were taken of the 3D Hoffman brain phantom on a GE Discovery IQ PET/CT scanner to test the ability of the radioactivity to indicate intra-scan motion. Each scan incrementally surveyed motion in a different degree of freedom (2 translational and 2 rotational). The radioactivity centroids calculated from these scans correlated linearly to phantom positions/orientations. Centroid measurements over 1-second intervals performed on scans with ~1mCi of activity in the center of the field of view had standard deviations of 0.026 cm in the x- and y-dimensions and 0.020 cm in the z-dimension, which demonstrates high precision and repeatability in this metric. Radioactivity centroids are thus shown to successfully represent discrete motions on the submillimeter scale. It is also shown that while the radioactivity centroid can precisely indicate the amount of motion during an acquisition, it fails to distinguish what type of motion occurred.
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La presenti tesi ha come obiettivo lo studio di due algoritmi per il rilevamento di anomalie all' interno di grafi random. Per entrambi gli algoritmi sono stati creati dei modelli generativi di grafi dinamici in modo da eseguire dei test sintetici. La tesi si compone in una parte iniziale teorica e di una seconda parte sperimentale. Il secondo capitolo introduce la teoria dei grafi. Il terzo capitolo presenta il problema del rilevamento di comunità. Il quarto capitolo introduce possibili definizioni del concetto di anomalie dinamiche e il problema del loro rilevamento. Il quinto capitolo propone l' introduzione di un punteggio di outlierness associato ad ogni nodo sulla base del confronto tra la sua dinamica e quella della comunità a cui appartiene. L' ultimo capitolo si incentra sul problema della ricerca di una descrizione della rete in termini di gruppi o ruoli sulla base della quale incentrare la ricerca delle anomalie dinamiche.
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Esophageal cancer is a prevalent cancer worldwide. Some studies have reported the possible etiology of human papillomavirus (HPV) in benign and malignant papillomas of the esophagus but the conclusions are controversial. In the present study, we investigated an esophageal papilloma from a 30-year-old male patient presenting aphasia. HPV DNA was detected by generic PCR using MY09/11 primers, and restriction fragment length polymorphism revealed the presence of HPV54, usually associated with benign genital lesions. Hypermethylation of the pINK4A gene was also investigated due to its relation to malignant transformation, but no modification was detected in the host gene. Except for an incipient reflux, no risk factors such as cigarette smoking, alcohol abuse or an infected sexual partner were recorded. Since esophageal lesions may have a malignant potential, HPV detection and typing are useful tools for patient follow-up.
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Die vorliegende Arbeit verfolgte mehrere Ziele. Die Hauptaufgabe war es, farbsensitive und bewegungssensitive Neurone im Tectum opticum des Goldfisches zu finden und diese hinsichtlich ihres Antwortverhaltens zu charakterisieren. Aus Verhaltensversuchen ist bekannt, dass sowohl das Ganzfeldbewegungssehen als auch das Objektbewegungssehen „farbenblind“ ist, da die Verarbeitung dieser Sehleistungen jeweils nur von einem Zapfentyp getrieben wird. Es sollte untersucht werden, ob sich diese Farbenblindheit auch auf Ebene der tectalen bewegungsempfindlichen Neurone finden lässt. Schließlich sollten die Ableitorte im Tectum opticum kartiert werden, um festzustellen, ob es jeweils bestimmte örtlich abgegrenzte Areale für Farbe einerseits und für Bewegung andererseits gibt.rnDie Aktivität von tectalen Units wurde durch extrazelluläre Ableitungen registriert. Um farbspezifische Neurone zu identifizieren und zu charakterisieren, wurden 21 verschiedene Farbpapiere (HKS-Standard) aus dem gesamten Farbenkreis (ausgenommen UV) präsentiert. Auf jedes Farbpapier folgte ein neutrales Graupapier. Des Weiteren wurde eine Schwarz-Weiß-Grau-Sequenz gezeigt, um das Antwortverhalten der Units auf Helligkeitswechsel zu prüfen. Jeder Stimulus wurde für fünf Sekunden präsentiert und die gesamte Stimulussequenz wurde mindestens dreimal wiederholt. Zur Identifizierung bewegungssensitiver Neurone wurde ein sich exzentrisch bewegendes schwarz-weißes Zufallspunktmuster präsentiert. Um die „Farbenblindheit“ des Bewegungssehens zu testen, wurden zwei rot-grüne Zufallspunktmuster präsentiert, die den L-Zapfen des Goldfisches unterschiedlich stark modulierten. Den meisten Units wurden sowohl die Farb- als auch die Bewegungsstimuli gezeigt.rnEs konnten 69 Units abgeleitet werden. Von diesen antworteten 34 sowohl auf Farbstimuli als auch auf Helligkeitsreize, 19 Units reagierten ausschließlich auf Farbstimuli, 15 Units zeigten sich nur für den Bewegungsstimulus sensitiv und zwei Units beantworteten ausschließlich Helligkeitswechsel. Die farbempfindlichen Units konnten in 14 Gruppen eingeteilt werden: sechs Gruppen im Rotbereich (22 Units), fünf Gruppen im Blau-Grünbereich (21 Units), eine Gruppe im Gelbbereich (zwei Units), eine Gruppe, die alle Farbstimuli mit Erhöhung der Aktivität (sechs Units) und eine Gruppe, die alle Farbstimuli mit Erniedrigung der Aktivität (eine Unit) beantwortete. Es wurden zwei Arten von Gegenfarbzellen gefunden: Rot-ON/Blau-und-Grün-OFF (12 Units) und Rot-OFF/Blau-und-Grün-ON (sieben Units). Es wurden verschiedene zeitliche Antwortmuster gefunden. Während einige Units nur Reizwechsel beantworteten, zeigten die meisten Units ein tonisches Antwortverhalten. Manche Units beantworteten jeden Stimuluswechsel phasisch und darüber hinaus bestimmte Stimuli tonisch. Die meisten tectalen Neurone zeigten eine Grundaktivität. Alle Units, denen sowohl der Farb- als auch der Bewegungsstimulus gezeigt wurden, antworteten nur auf eine Stimulusart. rnDiese Ergebnisse lassen folgende Schlüsse zu: Die Verarbeitung von Farbe und Bewegung im Tectum opticum des Goldfischs wird über zwei unterschiedlichen Verarbeitungswegen geleistet, da alle Units entweder auf Farb- oder auf Bewegungsstimuli antworten. Das Bewegungssehen wird im Goldfisch durch nur einen Zapfentyp (M- oder L-Zapfen) vermittelt und ist somit “farbenblind”, da alle bewegungssensitiven Units die Aktivität einstellten, wenn der Stimulus nur noch einen Zapfentyp modulierte. Es scheint spezifische Areale für „Farbe“ und „Bewegung“ im Tectum opticum des Goldfisches zu geben, da bewegungssensitive Units bevorzugt im posterio-medialen Bereich in einer Tiefe zwischen 200-400 µm gefunden und farbspezifische Units vor allem im anterio-medialen Bereich entdeckt wurden.
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Stimuli from one family of complex motions are defined by their spiral pitch, where cardinal axes represent signed expansion and rotation. Intermediate spirals are represented by intermediate pitches. It is well established that vision contains mechanisms that sum over space and direction to detect these stimuli (Morrone et al., Nature 376 (1995) 507) and one possibility is that four cardinal mechanisms encode the entire family. We extended earlier work (Meese & Harris, Vision Research 41 (2001) 1901) using subthreshold summation of random dot kinematograms and a two-interval forced choice technique to investigate this possibility. In our main experiments, the spiral pitch of one component was fixed and that of another was varied in steps of 15° relative to the first. Regardless of whether the fixed component was aligned with cardinal axes or an intermediate spiral, summation to-coherence-threshold between the two components declined as a function of their difference in spiral pitch. Similar experiments showed that none of the following were critical design features or stimulus parameters for our results: superposition of signal dots, limited life-time dots, the presence of speed gradients, stimulus size or the number of dots. A simplex algorithm was used to fit models containing mechanisms spaced at a pitch of either 90° (cardinal model) or 45° (cardinal+model) and combined using a fourth-root summation rule. For both models, direction half-bandwidth was equated for all mechanisms and was the only free parameter. Only the cardinal+model could account for the full set of results. We conclude that the detection of complex motion in human vision requires both cardinal and spiral mechanisms with a half-bandwidth of approximately 46°. © 2002 Elsevier Science Ltd. All rights reserved.
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Growing evidence from psychophysics and single-unit recordings suggests specialised mechanisms in the primate visual system for the detection of complex motion patterns such as expansion and rotation. Here we used a subthreshold summation technique to determine the direction tuning functions of the detecting mechanisms. We measured thresholds for discriminating noise and signal + noise for pairs of superimposed complex motion patterns (signal A and B) carried by random-dot stimuli in a circular 5° field. For expansion, rotation, deformation and translation we found broad tuning functions approximated by cos(d), where d is the difference in dot directions for signal A and B. These data were well described by models in which either: (a) cardinal mechanisms had direction bandwidths (half-widths) of around 60° or (b) the number of mechanisms was increased and their half-width was reduced to about 40°. When d = 180° we found summation to be greater than probability summation for expansion, rotation and translation, consistent with the idea that mechanisms for these stimuli are constructed from subunits responsive to relative motion. For deformation, however, we found sensitivity declined when d = 180°, suggesting antagonistic input from directional subunits in the deformation mechanism. This is a necessary property for a mechanism whose job is to extract the deformation component from the optic flow field. © 2001 Elsevier Science Ltd.
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Die Detektion von Bewegung stellt eine der fundamentalsten Fähigkeiten der visuellen Wahrnehmung dar. Um zu klären, ob das System zur Bewegungswahrnehmung Eingang nur durch einen Zapfentyp erhält, oder ob eine Kombination von verschiedenen Zapfentypen vorliegt, wurde eine rotierende zwei-armige archimedische Spiralscheibe verwendet (reale Bewegung), bei der sich Spirale und Hintergrund farblich unterschieden. Durch Veränderung der Intensität farbiger Leuchtstoffröhren konnte eine Beleuchtungssituation geschaffen werden, bei der die (radiale) Bewegung der Spirale nicht mehr wahrgenommen werden konnte, obwohl Spirale und Hintergrund farblich verschieden waren. Die Bestimmung der Zapfenerregungen im 3-D Rezeptorraum ließ einen Beitrag sowohl des L– als auch des M-Zapfens bei normalsichtigen Trichromaten (dominiert durch L), jedoch einen alleinigen Beitrag des M-Zapfens bei Protanopen erkennen. Die Ermittlung der spektralen Empfindlichkeit basierend auf einer Vektor Analyse im 3D-Rezeptorraum zeigte schließlich, dass dem neuronalen Bewegungsdetektor ein additiver Beitrag des L- und M-Zapfens, in Übereinstimmung mit der Hellempfindlichkeitsfunktion (Vλ), zugrunde liegt. Als Ergebnis schreiben wir die Detektion von Objektbewegung einem farbenblinden Mechanismus zu. Es ist sehr wahrscheinlich, dass der Magnozelluläre-Kanal das neuronale Substrat dieses Bewegungsdetektors repräsentiert.
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Active head turns to the left and right have recently been shown to influence numerical cognition by shifting attention along the mental number line. In the present study, we found that passive whole-body motion influences numerical cognition. In a random-number generation task (Experiment 1), leftward and downward displacement of participants facilitated small number generation, whereas rightward and upward displacement facilitated the generation of large numbers. Influences of leftward and rightward motion were also found for the processing of auditorily presented numbers in a magnitude-judgment task (Experiment 2). Additionally, we investigated the reverse effect of the number-space association (Experiment 3). Participants were displaced leftward or rightward and asked to detect motion direction as fast as possible while small or large numbers were auditorily presented. When motion detection was difficult, leftward motion was detected faster when hearing small number and rightward motion when hearing large number. We provide new evidence that bottom-up vestibular activation is sufficient to interact with the higher-order spatial representation underlying numerical cognition. The results show that action planning or motor activity is not necessary to influence spatial attention. Moreover, our results suggest that self-motion perception and numerical cognition can mutually influence each other.
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The hallucinogenic serotonin(IA&2A) agonist psilocybin is known for its ability to induce illusions of motion in otherwise stationary objects or textured surfaces. This study investigated the effect of psilocybin on local and global motion processing in nine human volunteers. Using a forced choice direction of motion discrimination task we show that psilocybin selectively impairs coherence sensitivity for random dot patterns, likely mediated by high-level global motion detectors, but not contrast sensitivity for drifting gratings, believed to be mediated by low-level detectors. These results are in line with those observed within schizophrenic populations and are discussed in respect to the proposition that psilocybin may provide a model to investigate clinical psychosis and the pharmacological underpinnings of visual perception in normal populations.