Abstract:Local motion signals have to be combined in space and time, to yield a coherent motion percept as it is involved in a variety of visual tasks. This combination necessarily means to trade-off between loosing spatio-temporal resolution by pooling local signals and maintaining perceptually significant segmentation between them. When signals are pooled to detect the presence of coherent motion in large amounts of random noise, the question raised is how the noise affects the perceived quality, in particular speed,… Show more
“…At a video frame-rate of 25 Hz, the default time constant was chosen to be 80 ms (two frames), which bestows the EMD with a temporal frequency optimum of approx. 2 Hz (see, e.g., Zanker & Braddick 1999). This tuning is well within the range of temporal frequency characteristics described for a variety of motion sensitive neurones in insects (O'Carroll et al 1997).…”
Section: Discussionsupporting
confidence: 75%
“…This model has been used previously to analyse species-specific movement signals in crabs (Zeil & Zanker 1997), and to simulate a variety of psychophysical phenomena (Zanker 1997;Zanker & Braddick 1999;Zanker 2004). The basic building blocks of the 2DMD model are elementary motion detectors (EMDs) of the correlation type, which have been shown to describe the computational structure of biological motion detectors at least in insects (for review, see Reichardt 1987;.…”
The movement of an observer generates a characteristic field of velocity vectors on the retina (Gibson 1950). Because such optic flow-fields are useful for navigation, many theoretical, psychophysical and physiological studies have addressed the question how ego-motion parameters such as direction of heading can be estimated from optic flow. Little is known, however, about the structure of optic flow under natural conditions. To address this issue, we recorded sequences of panoramic images along accurately defined paths in a variety of outdoor locations and used these sequences as input to a two-dimensional array of correlation-based motion detectors (2DMD). We find that (a) motion signal distributions are sparse and noisy with respect to local motion directions; (b) motion signal distributions contain patches (motion streaks) which are systematically oriented along the principal flow-field directions; (c) motion signal distributions show a distinct, dorso-ventral topography, reflecting the distance anisotropy of terrestrial environments; (d) the spatiotemporal tuning of the local motion detector we used has little influence on the structure of motion signal distributions, at least for the range of conditions we tested; and (e) environmental motion is locally noisy throughout the visual field, with little spatial or temporal correlation; it can therefore be removed by temporal averaging and is largely over-ridden by image motion caused by observer movement. Our results suggest that spatial or temporal integration is important to retrieve reliable information on the local direction and size of motion vectors, because the structure of optic flow is clearly detectable in the temporal average of motion signal distributions. Ego-motion parameters can be reliably retrieved from such averaged distributions under a range of environmental conditions. These observations raise a number of questions about the role of specific environmental and computational constraints in the processing of natural optic flow.
“…At a video frame-rate of 25 Hz, the default time constant was chosen to be 80 ms (two frames), which bestows the EMD with a temporal frequency optimum of approx. 2 Hz (see, e.g., Zanker & Braddick 1999). This tuning is well within the range of temporal frequency characteristics described for a variety of motion sensitive neurones in insects (O'Carroll et al 1997).…”
Section: Discussionsupporting
confidence: 75%
“…This model has been used previously to analyse species-specific movement signals in crabs (Zeil & Zanker 1997), and to simulate a variety of psychophysical phenomena (Zanker 1997;Zanker & Braddick 1999;Zanker 2004). The basic building blocks of the 2DMD model are elementary motion detectors (EMDs) of the correlation type, which have been shown to describe the computational structure of biological motion detectors at least in insects (for review, see Reichardt 1987;.…”
The movement of an observer generates a characteristic field of velocity vectors on the retina (Gibson 1950). Because such optic flow-fields are useful for navigation, many theoretical, psychophysical and physiological studies have addressed the question how ego-motion parameters such as direction of heading can be estimated from optic flow. Little is known, however, about the structure of optic flow under natural conditions. To address this issue, we recorded sequences of panoramic images along accurately defined paths in a variety of outdoor locations and used these sequences as input to a two-dimensional array of correlation-based motion detectors (2DMD). We find that (a) motion signal distributions are sparse and noisy with respect to local motion directions; (b) motion signal distributions contain patches (motion streaks) which are systematically oriented along the principal flow-field directions; (c) motion signal distributions show a distinct, dorso-ventral topography, reflecting the distance anisotropy of terrestrial environments; (d) the spatiotemporal tuning of the local motion detector we used has little influence on the structure of motion signal distributions, at least for the range of conditions we tested; and (e) environmental motion is locally noisy throughout the visual field, with little spatial or temporal correlation; it can therefore be removed by temporal averaging and is largely over-ridden by image motion caused by observer movement. Our results suggest that spatial or temporal integration is important to retrieve reliable information on the local direction and size of motion vectors, because the structure of optic flow is clearly detectable in the temporal average of motion signal distributions. Ego-motion parameters can be reliably retrieved from such averaged distributions under a range of environmental conditions. These observations raise a number of questions about the role of specific environmental and computational constraints in the processing of natural optic flow.
“…That is, the addition of the variability did not lead to an increase or decrease in the perceived stiffness of the force field. This is consistent with the findings of Zanker et al [49] who created different levels of noise in visual speed feedback. They observed that while the noise had no effect on the perceived speed, the noise impacted the certainty.…”
When interacting with objects, haptic information is used to create perception of the object stiffness and to regulate grip force. Studies have shown that introducing noise into sensory inputs can create uncertainty in those sensory channels, yet a method of creating haptic uncertainty without distorting the haptic information has yet to be discovered. Toward this end, we investigated the effect of between-probe haptic variability on stiffness perception and grip force control. In a stiffness discrimination task, we added different levels of between-probe haptic variability by changing the stiffness of the force fields between consecutive probes. Unlike the low and high variability levels, the medium level created perceptual haptic uncertainty. Additionally, we ascertained that participants calculated a weighted average of the different stiffness levels applied by a given force field. Examining participants' grip force showed that the modulation of the grip force with the load force decreased with repeated exposure to the force field, whereas no change in the baseline was observed. These results were observed in all the variability levels and suggest that between-probe variability created haptic uncertainty that affected the grip force control. Overall, the medium variability level can be effective in inducing uncertainty in both perception and action.
“…Unexpectedly, when the CS moved in front of the rDVN with the same physical speed as the SS, the proportion of "CS faster" responses was not above chance (0.5), even when the TMS was applied over the control site Cz. This is important because, statistically speaking, it is not possible to conclude that visual dynamic noise actually enhanced the perceived speed of a target as in previous studies (Edwards & Grainger, 2006;Zanker & Braddick, 1999). 1 On the other hand, in the SVN condition, with rTMS delivered over the Cz (control condition) and with the CS as fast as the SS, the proportion of "CS faster" responses was not below chance (0.5) and the BF (3.55) was clearly in favour of the null hypothesis.…”
Observers report seeing as slower a target disk moving in front of a static visual noise (SVN) background than the same object moving in front of a random dynamic visual noise (rDVN) background when the speed is the same. To investigate in which brain region (lower vs. higher visual areas) the background and the target signals might be combined to elicit this misperception, the transcranial magnetic stimulation (TMS) was delivered over the early visual cortex (V1/V2), middle temporal area (MT) and Cz (control site) while participants performed a speed discrimination task with targets moving in front of an SVN or an rDVN. Results showed that the TMS over MT reduced the perceived speed of the target moving in front of an SVN, but not when the target was moving in front of an rDVN background. Moreover, the TMS do not seem to interfere with encoding processing but more likely affected decoding processing in conditions of high uncertainty (i.e., when targets have similar speed).
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