scholarly journals Human Visuospatial Updating After Passive Translations in Three-Dimensional Space

2008 ◽  
Vol 99 (4) ◽  
pp. 1799-1809 ◽  
Author(s):  
Eliana M. Klier ◽  
Bernhard J. M. Hess ◽  
Dora E. Angelaki

To maintain a stable representation of the visual environment as we move, the brain must update the locations of targets in space using extra-retinal signals. Humans can accurately update after intervening active whole-body translations. But can they also update for passive translations (i.e., without efference copy signals of an outgoing motor command)? We asked six head-fixed subjects to remember the location of a briefly flashed target (five possible targets were located at depths of 23, 33, 43, 63, and 150 cm in front of the cyclopean eye) as they moved 10 cm left, right, up, down, forward, or backward while fixating a head-fixed target at 53 cm. After the movement, the subjects made a saccade to the remembered location of the flash with a combination of version and vergence eye movements. We computed an updating ratio where 0 indicates no updating and 1 indicates perfect updating. For lateral and vertical whole-body motion, where updating performance is judged by the size of the version movement, the updating ratios were similar for leftward and rightward translations, averaging 0.84 ± 0.28 (mean ± SD) as compared with 0.51 ± 0.33 for downward and 1.05 ± 0.50 for upward translations. For forward/backward movements, where updating performance is judged by the size of the vergence movement, the average updating ratio was 1.12 ± 0.45. Updating ratios tended to be larger for far targets than near targets, although both intra- and intersubject variabilities were smallest for near targets. Thus in addition to self-generated movements, extra-retinal signals involving otolith and proprioceptive cues can also be used for spatial constancy.

2003 ◽  
Vol 26 (4) ◽  
pp. 424-424
Author(s):  
Victor Rosenthal ◽  
Yves-Marie Visetti

Lehar (rightly) insists on the volumetric character of our experience of space. He claims that three-dimensional space stems from the functional three-dimensional topology of the brain. But his “Gestalt Bubble” model of volumetric space bears an intrinsically static structure – a kind of theater, or “diorama,” bound to the visual modality. We call attention to the ambivalence of Gestalt legacy and question the status and precise import of Lehar's model and the phenomenology that motivates it.


Author(s):  
Mahdi Khorram ◽  
S Ali A Moosavian

Legged robots have superior advantages rather than wheeled robots for moving over uneven terrains in the presence of various obstacles. The design of an appropriate path for the main body and legs is an important issue for such robots especially on the uneven terrains. In this paper, the focus is to develop a stable gait for a quadruped robot to trot on uneven terrains. First, a stability condition is developed for a whole-body quadruped robot over uneven terrains based on avoiding the tumbling. By using a simple model, a point with zero moments is calculated in the three-dimensional space. Then, the reference path of this point is determined so that the tumbling moments become zero. The path of the main body will be calculated by using an optimal controller. The main feature of the proposed gait generation framework is that the height of robot can change continuously and stably on uneven terrains. To evaluate the robot stability, the tumbling moments around diagonal lines are calculated and some methods are proposed to reduce these moments to improve the robot stability. The tip of swing foot is also planned to avoid any collision with the environment. The proposed method will be demonstrated using an 18-Degrees of freedom (DOF) quadruped robot in simulation and experimental studies. The experimental setup is a small-size quadruped robot, which is composed of a rectangular plate as its main body with four legs that each one has three active joints with DC servo motors. Obtained results reveal that the robot can trot on uneven terrains stably. Besides, the comparison with the previous methods approves the merits of proposed algorithm on uneven terrains.


2008 ◽  
Vol 100 (4) ◽  
pp. 1967-1982 ◽  
Author(s):  
Marion R. Van Horn ◽  
Kathleen E. Cullen

To redirect our gaze in three-dimensional space we frequently combine saccades and vergence. These eye movements, known as disconjugate saccades, are characterized by eyes rotating by different amounts, with markedly different dynamics, and occur whenever gaze is shifted between near and far objects. How the brain ensures the precise control of binocular positioning remains controversial. It has been proposed that the traditionally assumed “conjugate” saccadic premotor pathway does not encode conjugate commands but rather encodes monocular commands for the right or left eye during saccades. Here, we directly test this proposal by recording from the premotor neurons of the horizontal saccade generator during a dissociation task that required a vergence but no horizontal conjugate saccadic command. Specifically, saccadic burst neurons (SBNs) in the paramedian pontine reticular formation were recorded while rhesus monkeys made vertical saccades made between near and far targets. During this task, we first show that peak vergence velocities were enhanced to saccade-like speeds (e.g., >150 vs. <100°/s during saccade-free movements for comparable changes in vergence angle). We then quantified the discharge dynamics of SBNs during these movements and found that the majority of the neurons preferentially encode the velocity of the ipsilateral eye. Notably, a given neuron typically encoded the movement of the same eye during horizontal saccades that were made in depth. Taken together, our findings demonstrate that the brain stem saccadic burst generator encodes integrated conjugate and vergence commands, thus providing strong evidence for the proposal that the classic saccadic premotor pathway controls gaze in three-dimensional space.


1997 ◽  
Vol 84 (1) ◽  
pp. 176-178
Author(s):  
Frank O'Brien

The author's population density index ( PDI) model is extended to three-dimensional distributions. A derived formula is presented that allows for the calculation of the lower and upper bounds of density in three-dimensional space for any finite lattice.


2019 ◽  
Author(s):  
Jumpei Morimoto ◽  
Yasuhiro Fukuda ◽  
Takumu Watanabe ◽  
Daisuke Kuroda ◽  
Kouhei Tsumoto ◽  
...  

<div> <div> <div> <p>“Peptoids” was proposed, over decades ago, as a term describing analogs of peptides that exhibit better physicochemical and pharmacokinetic properties than peptides. Oligo-(N-substituted glycines) (oligo-NSG) was previously proposed as a peptoid due to its high proteolytic resistance and membrane permeability. However, oligo-NSG is conformationally flexible and is difficult to achieve a defined shape in water. This conformational flexibility is severely limiting biological application of oligo-NSG. Here, we propose oligo-(N-substituted alanines) (oligo-NSA) as a new peptoid that forms a defined shape in water. A synthetic method established in this study enabled the first isolation and conformational study of optically pure oligo-NSA. Computational simulations, crystallographic studies and spectroscopic analysis demonstrated the well-defined extended shape of oligo-NSA realized by backbone steric effects. The new class of peptoid achieves the constrained conformation without any assistance of N-substituents and serves as an ideal scaffold for displaying functional groups in well-defined three-dimensional space, which leads to effective biomolecular recognition. </p> </div> </div> </div>


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