Responses of pigeon vestibulocerebellar neurons to optokinetic stimulation. II. The 3-dimensional reference frame of rotation neurons in the flocculus

1993 ◽  
Vol 70 (6) ◽  
pp. 2647-2659 ◽  
Author(s):  
D. R. Wylie ◽  
B. J. Frost
Keyword(s):  
Dimensional Space ◽  
Three Dimensional ◽  
Receptive Fields ◽  
Semicircular Canals ◽  
Vertical Axis ◽  
Horizontal Axis ◽  
Monocular Stimulation ◽  
Contralateral Eye ◽  
Ipsilateral Stimulation ◽  
Stimulation Of

1. The complex spike activity of Purkinje cells in the flocculus in response to rotational flowfields was recorded extracellularly in anesthetized pigeons. 2. The optokinetic stimulus was produced by a rotating “planetarium projector.” A light source was placed in the center of a tin cylinder, which was pierced with numerous small holes. A pen motor oscillated the cylinder about its long axis. This apparatus was placed above the bird's head and the resultant rotational flow-field was projected onto screens that surrounded the bird on all four sides. The axis of rotation of the planetarium could be oriented to any position in three-dimensional space. 3. Two types of responses were found: vertical axis (VA; n = 43) neurons responded best to visual rotation about the vertical axis, and H-135i neurons (n = 34) responded best to rotation about a horizontal axis. The preferred orientation of the horizontal axis was at approximately 135 degrees ipsilateral azimuth. VA neurons were excited by rotation about the vertical axis producing forward (temporal to nasal) and backward motion in the ipsilateral and contralateral eyes, respectively, and were inhibited by rotation in the opposite direction. H-135i neurons in the left flocculus were excited by counterclockwise rotation about the 135 degrees ipsilateral horizontal axis and were inhibited by clockwise motion. Thus, the VA and H-135i neurons, respectively, encode visual flowfields resulting from head rotations stimulating the ipsilateral horizontal and ipsilateral anterior semicircular canals. 4. Sixty-seven percent of VA and 80% of H-135i neurons had binocular receptive fields, although for most binocular cells the ipsilateral eye was dominant. Binocular stimulation resulted in a greater depth of modulation than did monocular stimulation of the dominant eye for 69% of the cells. 5. Monocular stimulation of the VA neurons revealed that the best axis for the contralateral eye was tilted back 11 degrees, on average, to the best axis for ipsilateral stimulation. For the H-135i neurons, the best axes for monocular stimulation of the two eyes were approximately the same. 6. By stimulating circumscribed portions of the monocular receptive fields of the H-135i neurons with alternating upward and downward largefield motion, it was revealed that the contralateral receptive fields were bipartite. Upward motion was preferred in the anterior 45 degrees of the contralateral field, and downward motion, was preferred in the central 90 degrees of the contralateral visual field.(ABSTRACT TRUNCATED AT 400 WORDS)

Navigating in a volumetric world: Metric encoding in the vertical axis of space

2013 ◽  
Vol 36 (5) ◽  
pp. 546-547 ◽  
Author(s):  
Theresa Burt de Perera ◽  
Robert Holbrook ◽  
Victoria Davis ◽  
Alex Kacelnik ◽  
Tim Guilford
Keyword(s):  
Spatial Information ◽  
Dimensional Space ◽  
Three Dimensional ◽  
Vertical Component ◽  
Vertical Axis ◽  
Orthogonal Axis ◽  
Experimental Protocols ◽  
Three Dimensional Space ◽  
The Way

AbstractAnimals navigate through three-dimensional environments, but we argue that the way they encode three-dimensional spatial information is shaped by how they use the vertical component of space. We agree with Jeffery et al. that the representation of three-dimensional space in vertebrates is probably bicoded (with separation of the plane of locomotion and its orthogonal axis), but we believe that their suggestion that the vertical axis is stored “contextually” (that is, not containing distance or direction metrics usable for novel computations) is unlikely, and as yet unsupported. We describe potential experimental protocols that could clarify these differences in opinion empirically.

Measurement of the Shortening Effect on the Perceived Path of Stroboscopic Movement

Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 288-288
Author(s):  
S Nozawa
Keyword(s):  
Three Dimensional ◽  
Vertical Axis ◽  
Horizontal Axis ◽  
The Other ◽  
Horizontal Line ◽  
Optimal Frequency ◽  
Stimulus Line ◽  
Factors Influencing ◽  
Parallel Motion ◽  
Axis I

When two vertical short lines are alternately flashed at certain SOAs, a shortening of the apparent path of the stroboscopic movement is perceived. In the experiments reported here, factors influencing the shortening effect were studied with lines created on a CRT display. Experiment 1 was designed to study the effect of SOA. Each stimulus line was always presented for 100 ms, but intervals were varied in the range from 25 to 800 ms. With short and long SOAs almost no shortening illusion was observed, whereas the SOA for optimal stroboscopic motion (200 ms) also produced the largest illusion (ca 16%). This agrees with the classic study by Scholz (1924 Psychologische Forschung5 219 – 272) who found the largest illusion (25%) at the optimal frequency for stroboscopic motion. Experiment 2 dealt with the effect of inversions (I), mirror reflections (M), and rotations (R) of the line during the stroboscopic movement (see Kolars and Pomerantz, 1971 Journal of Experimental Psychology87 99 – 108). The particular movements were signalled by means of a short horizontal line added to one end of each of the two vertical lines of experiment 1. The configurations were (1), signifying parallel motion in one plane; (2), locomotion with rotation around the vertical axis (M); (3), locomotion with rotation around the horizontal axis (I); and (4), locomotion with rotation in the plane of the display (R). In all these conditions, the shortening illusion was significantly larger than in experiment 1. The differences between the four conditions were not statistically significant, but the illusion under condition (1) seemed smaller than in the other three conditions. With SOAs for optimal stroboscopic motion, ‘rotation’ paths tended to appear three-dimensional.

Cutaneous Receptive Field Organization in the Ventral Posterior Nucleus of the Thalamus in the Common Marmoset

1999 ◽  
Vol 82 (4) ◽  
pp. 1865-1875 ◽  
Author(s):  
P. Wilson ◽  
P. D. Kitchener ◽  
P. J. Snow
Keyword(s):  
Dimensional Space ◽  
Three Dimensional ◽  
Receptive Fields ◽  
Common Marmoset ◽  
The Body ◽  
Common Marmosets ◽  
Body Regions ◽  
Low Threshold ◽  
The Common ◽  
Receptive Field Organization

The organization of cutaneous receptive fields in the ventroposterior (VP) thalamus of the common marmosets ( Callithrix jacchus) was determined from single-unit recordings, and these data were correlated with the cytochrome oxidase (CO) histochemistry of the thalamus in the same animals. Under continuously maintained ketamine anesthesia, the receptive fields of a total of 192 single units were recorded from the right VP thalamus using 2 MΩ glass microelectrodes. After the receptive fields were mapped, the brains were reacted for CO histochemistry on 50-μm coronal frozen sections through the entire VP thalamus. The majority of units were localized to the CO-reactive regions that define the medial and lateral divisions of VP (VPm and VPl). Apart from the expected finding of the face being represented in VPm and the body in VPl, reconstructing the electrode tracks and unit locations in the histological sections revealed a general association between discrete regions of CO reactivity and the representation of specific body regions. Some low-threshold cutaneous units were apparently localized to VPi (the CO weak regions dorsal, ventral, and interdigitating with, the CO regions of VP). These VPi units were clearly part of the same representational map as the VPl and VPm units. We conclude that the low-threshold cutaneous receptive fields of the marmoset are organized in a single continuous representation of the contralateral body surface, and that this representation can most simply be interpreted as being folded or crumpled into the three-dimensional space of VP thalamus. The folded nature of the body map in VP may be related to the folded nature of VP as revealed by CO histochemistry.

scholarly journals Viewing-patterns and perspectival painting: An eye-tracking study on the effect of the vanishing point

2021 ◽  
Vol 13 (2) ◽  
Author(s):  
Arthur Crucq
Keyword(s):  
Eye Tracking ◽  
Dimensional Space ◽  
Three Dimensional ◽  
Vertical Axis ◽  
Picture Plane ◽  
Linear Perspective ◽  
Underlying Structure ◽  
Vanishing Point ◽  
Visual Feature ◽  
The Gaze

Linear perspective has long been used to create the illusion of three-dimensional space on the picture plane. One of its central axioms comes from Euclidean geometry and holds that all parallel lines converge in a single vanishing point. Although linear perspective provided the painter with a means to organize the painting, the question is whether the gaze of the beholder is also affected by the underlying structure of linear perspective: for instance, in such a way that the orthogonals leading to the vanishing point also automatically guides the beholder’s gaze. This was researched during a pilot study by means of an eye-tracking experiment at the Lab for Cognitive Research in Art History (CReA) of the University of Vienna. It appears that in some compositions the vanishing point attracts the view of the participant. This effect is more significant when the vanishing point coincides with the central vertical axis of the painting, but is even stronger when the vanishing point also coincides with a major visual feature such as an object or figure. The latter calls into question what exactly attracts the gaze of the viewer, i.e., what comes first: the geometrical construct of the vanishing point or the visual feature?

scholarly journals Semicircular canal biomechanics in health and disease

2019 ◽  
Vol 121 (3) ◽  
pp. 732-755 ◽  
Author(s):  
R. D. Rabbitt
Keyword(s):  
Time Course ◽  
Dimensional Space ◽  
Three Dimensional ◽  
Semicircular Canals ◽  
Head Movements ◽  
Positional Nystagmus ◽  
Neural Encoding ◽  
Range Of Movement ◽  
Stable Vision ◽  
Health And Disease

The semicircular canals are responsible for sensing angular head motion in three-dimensional space and for providing neural inputs to the central nervous system (CNS) essential for agile mobility, stable vision, and autonomic control of the cardiovascular and other gravity-sensitive systems. Sensation relies on fluid mechanics within the labyrinth to selectively convert angular head acceleration into sensory hair bundle displacements in each of three inner ear sensory organs. Canal afferent neurons encode the direction and time course of head movements over a broad range of movement frequencies and amplitudes. Disorders altering canal mechanics result in pathological inputs to the CNS, often leading to debilitating symptoms. Vestibular disorders and conditions with mechanical substrates include benign paroxysmal positional nystagmus, direction-changing positional nystagmus, alcohol positional nystagmus, caloric nystagmus, Tullio phenomena, and others. Here, the mechanics of angular motion transduction and how it contributes to neural encoding by the semicircular canals is reviewed in both health and disease.

Responses of Neurons in the Nucleus of the Basal Optic Root to Translational and Rotational Flowfields

1999 ◽  
Vol 81 (1) ◽  
pp. 267-276 ◽  
Author(s):  
Douglas R. W. Wylie ◽  
Barrie J. Frost
Keyword(s):  
Optic Flow ◽  
Horizontal Plane ◽  
Dimensional Space ◽  
Three Dimensional ◽  
Vertical Axis ◽  
Mesencephalic Reticular Formation ◽  
Companion Paper ◽  
Direction Selectivity ◽  
Large Field ◽  
Adjacent Area

Wylie, Douglas R. W. and Barrie J. Frost. Responses of Neurons in the nucleus of the basal optic root to translational and rotational flowfields. J. Neurophysiol. 81: 267–276, 1999. The nucleus of the basal optic root (nBOR) receives direct input from the contralateral retina and is the first step in a pathway dedicated to the analysis of optic flowfields resulting from self-motion. Previous studies have shown that most nBOR neurons exhibit direction selectivity in response to large-field stimuli moving in the contralateral hemifield, but a subpopulation of nBOR neurons has binocular receptive fields. In this study, the activity of binocular nBOR neurons was recorded in anesthetized pigeons in response to panoramic translational and rotational optic flow. Translational optic flow was produced by the “translator” projector described in the companion paper, and rotational optic flow was produced by a “planetarium projector” described by Wylie and Frost. The axis of rotation or translation could be positioned to any orientation in three-dimensional space. We recorded from 37 cells, most of which exhibited a strong contralateral dominance. Most of these cells were located in the caudal and dorsal aspects of the nBOR complex and many were localized to the subnucleus nBOR dorsalis. Other units were located outside the boundaries of the nBOR complex in the adjacent area ventralis of Tsai or mesencephalic reticular formation. Six cells responded best to rotational flowfields, whereas 31 responded best to translational flowfields. Of the rotation cells, three preferred rotation about the vertical axis and three preferred horizontal axes. Of the translation cells, 3 responded best to a flowfield simulating downward translation of the bird along a vertical axis, whereas the remaining 28 responded best to flowfields resulting from translation along axes in the horizontal plane. Seventeen of these cells preferred a flowfield resulting from the animal translating backward along an axis oriented ∼45° to the midline, but the best axes of the remaining eleven cells were distributed throughout the horizontal plane with no definitive clustering. These data are compared with the responses of vestibulocerebellar Purkinje cells.

Analysis of the Effect of a Slotted Flap Mechanism on the Performance of an H-Darrieus Turbine Using CFD

2014 ◽  
Author(s):  
László Daróczy ◽  
Mohamed H. Mohamed ◽  
Gábor Janiga ◽  
Dominique Thévenin
Keyword(s):  
Three Dimensional ◽  
Vertical Axis ◽  
Operating Conditions ◽  
Horizontal Axis ◽  
Pollutant Emissions ◽  
Power Coefficient ◽  
Major Drawback ◽  
Systematic Analysis ◽  
Low Wind Speed ◽  
Low Efficiency

Wind energy represents nowadays a very important source of energy for many countries. It provides an efficient and effective solution to reduce fuel consumption as well as pollutant emissions. VAWTs (vertical axis wind turbines) were originally considered as very promising, before being superseded by the present, horizontal axis turbines. There is now a resurgence of interests for VAWTs, in particular Darrieus turbines. VAWTs like the H-rotor Darrieus turbine appear to be particularly promising for low wind speed conditions, but suffer from a low efficiency compared to horizontal axis turbines. Additionally, Darrieus turbines are not self-starting, which is a major drawback. The present paper introduces a new idea to improve the global performance of Darrieus rotors, relying on a slotted flap. Due to its low manufacturing costs and size, a two-bladed H-rotor with a radius of 2 meters was retained as a first application example. The blade airfoil relies on the S1046 profile, which was shown in previous studies to be superior under relevant operating conditions [1]. The solidity (Nc/R) of the rotor is kept at 0.25 for all the computations. In the first step a parametric geometry is created, where the end of the blade is converted into a slotted flap (with appropriate rounding). The main parameters are the distance between the main part of the blade and the flap (width of gap), the angle of the slot and the angle of the flap. In the second step a systematic analysis of the effect of those variables on the force and power coefficient is carried out using three-dimensional full factorial Design-of-Experiment with an in-house parameterization and optimization software. For each configuration, force and power coefficients are calculated for four different tip-speed ratios (including the value, where the S1046 profile without flap shows its maximal power coefficient). The evaluation of each configuration is performed using a commercial CFD software. The flow is assumed in this first study to be two-dimensional and unsteady. Turbulence intensities follow the relevant norms (DIN EN 61400). Finally the results are compared to each other and to the reference design (S1046 without flap) and conclusions are given regarding power coefficient and flap load.

scholarly journals The Life Mission Theory III. Theory of Talent

2003 ◽  
Vol 3 ◽  
pp. 1286-1293 ◽  
Author(s):  
Soren Ventegodt ◽  
Niels Jorgen Andersen ◽  
Joav Merrick
Keyword(s):  
Dimensional Space ◽  
Three Dimensional ◽  
Vertical Axis ◽  
Three Dimensions ◽  
Natural State ◽  
Human Form ◽  
The World ◽  
Sex And Sexuality ◽  
And Gender ◽  
Third Dimension

When we acknowledge our purpose as the essence of our self, when we take all our power into use in an effortless way, and when we fully accept our own nature — including sex and sexuality, our purpose of life takes the form of a unique talent. Using this talent gives the experience of happiness. A person in his natural state of being uses his core talent in a conscious, joyful, and effortless way, contributing to the world the best he or she has to offer. Full expression of self happens when a person, in full acceptance of body and life, with whole-hearted intension, uses all his personal powers to realize his core talent and all associated talents, to contribute to his beloved and to the world. Thus, self-actualisation is a result of a person fully expressing and realizing his core talent.The theory of talent states that a core talent can be expressed optimally when a human being takes possession of a three-dimensional space with the axis of purpose, power and gender, as we have a threefold need: 1-Acknowledging our core talent (our purpose of life) and intending it 2-Understanding our potential powers and manifesting them 3-Accepting our human form including our sex and expressing itThe first dimension is spiritual, the next dimension is mental, emotional and physical, and the third dimension is bodily and sexual. We manifest our talents in a giving movement from the bottom of our soul trough our biological nature onto the subject and object of the outer world. These three dimensions can be drawn as three axes, one saggital axis called purpose or love or me-you, one vertical axis called power or consciousness (light) or heaven-earth, and one horizontal axis called gender or joy or male-female. The three core dimensions of human existence are considered of equal importance for expression of our life purpose, life mission, or core talent. Each of the dimensions is connected to special needs. When these needs are not fulfilled, we suffer and if this suffering becomes unbearable we deny the dimension or a part of is. This is why the dimensions of purpose, power and gender become suppressed from our consciousness.

Importance of corpus callosum for visual receptive fields of single neurons in cat superior colliculus

1979 ◽  
Vol 42 (1) ◽  
pp. 137-152 ◽  
Author(s):  
A. Antonini ◽  
G. Berlucchi ◽  
C. A. Marzi ◽  
J. M. Sprague
Keyword(s):  
Visual Field ◽  
Corpus Callosum ◽  
Superior Colliculus ◽  
Visual Information ◽  
Visual Learning ◽  
Receptive Fields ◽  
Vertical Meridian ◽  
Retinotectal Projections ◽  
Contralateral Eye ◽  
Stimulation Of

1. Section of the posterior two-thirds of the corpus callosum eliminates almost completely the response of superior colliculus (SC) neurons to stimulation of the contralateral eye in split-chiasm cats. On the contrary, the responsiveness of SC neurons to stimulation of the contralateral eye is not abolished by a transection of the posterior and tectal commissures leaving the corpus callosum intact. The callosal section also reduces the number of SC receptive fields abutting the vertical meridian in the ipsilateral eye of split-chiasm cats. 2. In cats with intact optic pathways, a similar callosal section abolishes the SC representation of the ipsilateral visual field in the ipsilateral eye and also reduces the number of receptive fields adjoining the vertical meridian in the same eye. In the contralateral eye, the SC representation of the ipsilateral visual field is reduced in extension to about one-fifth of that seen in cats with intact commissures. 3. The results suggest that the corpus callosum is the main pathway for cross-midline communication of visual information at not only the cortical, but also the midbrain level. The corpus callosum may subserve this function because it contains uninterrupted crossed corticotectal projections or because it transmits visual information from one hemisphere to contralateral cortical areas projecting ipsilaterally to SC. The latter hypothesis is more likely but, in any case, the findings imply that the lack of interhemispheric transfer of visual learning in cats with a chiasmatic and callosal section may depend on a midline disconnection of both subcortical and cortical visual centers. 4. The corpus callosum is also responsible for the representation of the ipsilateral visual field of the ipsilateral eye in the cat SC. The SC representation of the ipsilateral visual field in the contralateral eye is due, in minimal part, to direct retinotectal connections from temporal retina and, for the largest part, to the corpus callosum. 5. Finally, the corpus callosum contributes to the representation of the contralateral visual field near the vertical meridian of the temporal retina in both split-chiasm and normal cats. This is probably due to the scarcity of direct retinotectal projections from this part of the retina and to their supplementation by corticotectal neurons influenced by the callosal afferents.

Three-dimensional organization of optokinetic responses in the rabbit

1993 ◽  
Vol 69 (2) ◽  
pp. 303-317 ◽  
Author(s):  
H. S. Tan ◽  
J. van der Steen ◽  
J. I. Simpson ◽  
H. Collewijn
Keyword(s):  
Control System ◽  
Horizontal Plane ◽  
Three Dimensional ◽  
Vertical Axis ◽  
Horizontal Axis ◽  
Constant Speed ◽  
Slow Phase ◽  
Optokinetic Stimulation ◽  
Axis Orientation ◽  
Maximum Gain

1. Three-dimensional rotations of both eyes were measured in alert rabbits during optokinetic stimulation about axes lying in the horizontal plane or about an earth-vertical axis, with either one or both eyes viewing the stimulus. Optokinetic stimulus speed was 2 degrees /s, either continuous or alternating in polarity (triangular stimulus). In addition to the gains of the responses, the orientations of the response axes relative to the stimulus axes were determined. 2. In comparison to the response to constant-speed optokinetic stimulation about the vertical axis, the response to constant-speed optokinetic stimulation about horizontal axes was characterized by the lack of a speed buildup. In many cases, slow phase tracking was good as long as the eye was within the central oculomotor range but deteriorated when eye deviation became more eccentric and fast phases failed to be generated. These features suggest that the optokinetic reflex about horizontal axes functions as a position-control system, rather than as a velocity-control system. 3. Binocular optokinetic stimulation at constant speed (2 degrees/s) about the roll axis (0 degrees azimuth horizontal axis) elicited disconjugate responses. Although the gain of the response was not significantly different in the two eyes (0.38 for downward and 0.44 for upward stimulation), the response axes of the two eyes differed by as much as 51 degrees. 4. Monocular, horizontal axis optokinetic stimulation at constant speed elicited responses that were grossly dissociated between the two eyes. The magnitude of the responses was anisotropic in that it varied with the azimuthal orientation of the stimulus axis; the maximum gain for each eye (0.41 for the seeing and 0.33 for the covered eye) was at 135 degrees azimuth for each eye. The axis orientation and direction (sense of rotation) of the optokinetic stimulus eliciting the maximal response for each eye coincided with the optic flow normally associated with the maximal excitation of the corresponding ipsilateral anterior canal. 5. Binocular, triangular optokinetic stimulation with small excursions (+/- 10 degrees), which avoided the saturation problems of constant-speed stimulation, elicited adequate responses without systematic directional asymmetries. Gain was approximately 0.9 for all stimulus axis orientations in the horizontal plane. 6. During monocular stimulation with triangular stimuli, the response of the seeing eye showed a gain of approximately 0.5 for all orientations of the stimulus axis. In contrast, the covered eye showed anisotropic responses, with a maximum gain of approximately 0.5 during stimulation of the seeing eye about its 45 degree axis.(ABSTRACT TRUNCATED AT 400 WORDS)

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