Sensitivity of MST neurons to optic flow stimuli. I. A continuum of response selectivity to large-field stimuli

1991 ◽  
Vol 65 (6) ◽  
pp. 1329-1345 ◽  
Author(s):  
C. J. Duffy ◽  
R. H. Wurtz

1. Neurons in the dorsomedial region of the medial superior temporal area (MSTd) have large receptive fields that include the fovea, are directionally selective for moving visual stimuli, prefer the motion of large fields to small spots, and respond to rotating and expanding patterns of motion as well as frontal parallel planar motion. These characteristics suggested that these neurons might contribute to the analysis of the large-field optic flow stimulation generated as an observer moves through the visual environment. 2. We tested the response of MSTd neurons in two awake monkeys by systematically presenting a set of translational and rotational stimuli to each neuron. These 100 X 100 degrees stimuli were the motion components from which all optic flow fields are derived. 3. In 220 single neurons we found 23% that responded primarily to one component of motion (planar, circular, or radial), 34% that responded to two components (planocircular or planoradial, but never circuloradial), and 29% that responded to all three components. 4. The number of stimulus components to which a neuron responded was unrelated to the size or eccentricity of its receptive field. 5. Triple-, double-, and single-component neurons varied widely in the strength of their responses to the preferred components. Grouping these neurons together revealed that they did not form discrete classes but rather a continuum of response selectivity. 6. This continuum was apparent in other response characteristics. Direction selectivity was weakest in triple-component neurons, strongest in single-component neurons. Significant inhibitory responses were less frequent in triple-component neurons than in single-component neurons. 7. There was some indication that the neurons of similar component classes occupied adjacent regions within MSTd, but all combinations of component and direction selectivity were occasionally found in immediate juxtaposition. 8. Experiments on a subset of neurons showed that the speed of motion, the dot density, and the number of different speed planes in the display had little influence on these responses. 9. We conclude that the selective responses of many MSTd neurons to the rotational and translational components of optic flow make these neurons reasonable candidates for contributing to the analysis of optic flow fields.

1998 ◽  
Vol 80 (4) ◽  
pp. 1816-1827 ◽  
Author(s):  
Charles J. Duffy

Duffy, Charles J. MST neurons respond to optic flow and translational movement . J. Neurophysiol. 80: 1816–1827, 1998. We recorded the responses of 189 medial superior temporal area (MST) neurons by using optic flow, real translational movement, and combined stimuli in which matching directions of optic flow and real translational movement were presented together. One-half of the neurons (48%) showed strong responses to optic flow simulating self-movement in the horizontal plane, and 24% showed strong responses to translational movement. Combining optic flow stimuli with matching directions of translational movement caused substantial changes in both the amplitude of the best responses (44% of neurons) and the strength of direction selectivity (71% of neurons), with little effect on which stimulus direction was preferred. However, combining optic flow and translational movement such that opposite directions were presented together changed the preferred direction in 45% of the neurons with substantial changes in the strength of direction selectivity. These studies suggest that MST neurons combine visual and vestibular signals to enhance self-movement detection and disambiguate optic flow that results from either self-movement or the movement of large objects near the observer.


1991 ◽  
Vol 65 (6) ◽  
pp. 1346-1359 ◽  
Author(s):  
C. J. Duffy ◽  
R. H. Wurtz

1. In these experiments we examined the receptive field mechanisms that support the optic flow field selective responses of neurons in the dorsomedial region of the medial superior temporal area (MSTd). Our experiments tested the predictions of two hypotheses of optic flow field selectivity. The direction mosaic hypothesis states that these receptive fields contain a set of planar direction-selective subfields that match the local directions of motion within optic flow fields. The vector field hypothesis states that these receptive fields are uniquely sensitive to distributed properties of planar, circular, or radial optic flow fields. 2. Experiments using large-field stimuli revealed that some neurons showed changes in optic flow field selectivity depending on the position of the stimulus in the receptive field; these are position-dependent responses. However, other neurons maintained the same optic flow field selectivities in spite of changes in stimulus position; these are position-invariant responses. We have used the position dependence or invariance of optic flow field selectivity as a way of testing the direction mosaic and vector field hypotheses. Position dependence is more consistent with the direction mosaic hypothesis, whereas position invariance is more consistent with the vector field hypothesis. 3. To test for position effects, we examined the optic flow field selectivity of small subfields within the large receptive fields of 160 MSTd neurons. First, we centered small-field optic flow stimuli of various sizes over the same position in the receptive field. Most MSTd neurons showed decreasing response amplitude with decreasing stimulus size but maintained optic flow field selectivity. 4. We then placed small-field stimuli at various positions within the large receptive field of these MSTd neurons. Position-invariant response selectivity was most prominent in single-component neurons, suggesting that they were more consistent with the vector field hypothesis. Position-dependent response selectivity was most prominent in triple-component neurons, suggesting that they were more consistent with the direction mosaic hypothesis. However, the variations in planar direction preference throughout the receptive field of these triple-component neurons were not consistent with a direction mosaic explanation of the large-field circular or radial selectivity observed. 5. Small-field position studies also demonstrated the existence of zones within the receptive field in which either direction-selective inhibitory or direction-selective excitatory responses predominated. The degree of overlap between these zones increased from nonselective to triple- to double- and finally to single-component neurons.(ABSTRACT TRUNCATED AT 400 WORDS)


2002 ◽  
Vol 88 (4) ◽  
pp. 1777-1790 ◽  
Author(s):  
Emad N. Eskandar ◽  
John A. Assad

We examined neuronal signals in the monkey medial superior temporal area (MST), the medial intraparietal area (MIP), and the lateral intraparietal area (LIP) during visually guided hand movements. Two animals were trained to use a joystick to guide a spot to a target. Many neurons responded in a direction-selective manner in this guidance task. We tested whether the direction selectivity depended on the direction of the stimulus spot or the direction of the hand movement. First, in some trials, the moving spot disappeared transiently. Second, the mapping between the hand direction and the spot direction was reversed on alternate blocks of trials. Third, we recorded the spot's movement while the animals moved the joystick and then played back that movement while the animals fixated without moving the joystick. Neurons in the three parietal areas conveyed distinct directional information. MST neurons were active and directional only on visible trials in both joystick-movement mode and playback mode and were not affected by the direction of hand movement. MIP neurons were mainly directional with respect to the hand movement, although some MIP neurons were also selective for stimulus direction. MIP neurons were much less active in playback mode. LIP neurons were active and directional in both joystick-movement mode and playback mode. Directional signals in LIP were unrelated to planning saccades. The selectivity of LIP neurons also became evident hundreds of milliseconds before the start of movement. Since the direction of movement was consistent throughout a block of trials, these signals could provide a prediction of the upcoming direction of motion. We tested this by alternating blocks of trials in which the direction was consistent or randomized. The direction selectivity developed earlier on trials in which the upcoming direction could be predicted. These results suggest that LIP neurons combine “bottom-up” visual motion signals with extraretinal, predictive signals about stimulus motion.


1997 ◽  
Vol 14 (4) ◽  
pp. 633-646 ◽  
Author(s):  
S.J. Schaafsma ◽  
J. Duysens ◽  
C.C.A.M. Gielen

AbstractThere is evidence that neurons in medial superior temporal area (MST) respond to rotation in depth of textured planes. MST neurons project to the ventral intraparietal area (VIP) and the question arises whether VIP neurons are responsive to rotation in depth as well. In the present study on awake monkeys, we have simulated movement of a flat board, covered with dots, by a computer. The two-dimensional images corresponded to the projection of structured planes rotating around a fronto-parallel axis. In the literature this stimulus is called fanning. Fanning effectively induced responses in VIP neurons. Most often the responses were nearly as strong as for translation, expansion/contraction, or rotation, indicating that there was no special sensitivity for rotation in depth. For neurons, sensitive to expansion, the response to fanning could often be explained by the positioning of the expanding part of the fanning stimulus over the area which was most responsive to expansion. For neurons which were direction selective to translation, the optimal direction of fanning was usually the same as the preferred direction for translation. It is concluded that VIP neurons may be sensitive to movement of structured planes but they are not specialized for the detection of such movement.


1996 ◽  
Vol 76 (6) ◽  
pp. 4056-4068 ◽  
Author(s):  
S. J. Schaafsma ◽  
J. Duysens

1. Neurons in the ventral intraparietal area (VIP) are known to respond to translating random dot patterns. Such responses can be explained on the basis of the input of the middle temporal area (MT) to this area. Anatomic evidence has shown that VIP receives input from the dorsal part of the medial superior temporal area (MSTd) also. Neurons in the latter area are though to be involved in egomotion because they are sensitive to first-order optic flow components such as divergence and rotation. Because of their MT and MSTd input, neurons in VIP may be expected to show sensitivity to such first-order optic flow as well. 2. The question of whether VIP neurons are selective to translation and/or first-order optic flow was investigated quantitatively in two awake monkeys by recording the responses of 52 visually responsive units and by fitting their tuning curves. The responses after presentation of random dot patterns exhibiting either expansion, contraction, clockwise rotation, or anticlockwise rotation were compared with the responses to translation stimuli tested in eight directions. 3. Most VIP neurons showed clear direction-selective responses, particularly to expansion but sometimes also to a combination of components (spiral stimuli). 4. A typical feature of VIP neurons is that their responses to these optic flow components remain when different parts of the receptive field are stimulated separately (“scale invariance”). For the most responsive subfield the response was on average 93% of the whole field response. For all subfields the mean response was on average 64% of the whole field response. 5. To test whether the scale invariance arose from convergence of translation-sensitive subfields with radial or circular direction preferences (“mosaic hypothesis”), the direction selectivity for translating stimuli was tested over these subfields. Basically the direction selectivity for translation was unchanged in the various subfields, thereby excluding the direction mosaic hypothesis. 6. It is concluded that the receptive field characteristics of VIP are very similar to those of MSTd neurons.


2001 ◽  
Vol 85 (2) ◽  
pp. 724-734 ◽  
Author(s):  
Holger G. Krapp ◽  
Roland Hengstenberg ◽  
Martin Egelhaaf

Integrating binocular motion information tunes wide-field direction-selective neurons in the fly optic lobe to respond preferentially to specific optic flow fields. This is shown by measuring the local preferred directions (LPDs) and local motion sensitivities (LMSs) at many positions within the receptive fields of three types of anatomically identifiable lobula plate tangential neurons: the three horizontal system (HS) neurons, the two centrifugal horizontal (CH) neurons, and three heterolateral connecting elements. The latter impart to two of the HS and to both CH neurons a sensitivity to motion from the contralateral visual field. Thus in two HS neurons and both CH neurons, the response field comprises part of the ipsi- and contralateral visual hemispheres. The distributions of LPDs within the binocular response fields of each neuron show marked similarities to the optic flow fields created by particular types of self-movements of the fly. Based on the characteristic distributions of local preferred directions and motion sensitivities within the response fields, the functional role of the respective neurons in the context of behaviorally relevant processing of visual wide-field motion is discussed.


1999 ◽  
Vol 82 (5) ◽  
pp. 2462-2475 ◽  
Author(s):  
Satoshi Eifuku ◽  
Robert H. Wurtz

Many neurons in the lateral-ventral region of the medial superior temporal area (MSTl) have a clear center surround separation in their receptive fields. Either moving or stationary stimuli in the surround modulates the response to moving stimuli in the center, and this modulation could facilitate the perceptual segmentation of a moving object from its background. Another mechanism that could facilitate such segmentation would be sensitivity to binocular disparity in the center and surround regions of the receptive fields of these neurons. We therefore investigated the sensitivity of these MSTl neurons to disparity ranging from three degrees crossed disparity (near) to three degrees uncrossed disparity (far) applied to both the center and the surround regions. Many neurons showed clear disparity sensitivity to stimulus motion in the center of the receptive field. About [Formula: see text] of 104 neurons had a clear peak in their response, whereas another [Formula: see text] had broader tuning. Monocular stimulation abolished the tuning. The prevalence of cells broadly tuned to near and far disparity and the reversal of preferred directions at different disparities observed in MSTd were not found in MSTl. A stationary surround at zero disparity simply modulated up or down the response to moving stimuli at different disparities in the receptive field (RF) center but did not alter the disparity tuning curve. When the RF center motion was held at zero disparity and the disparity of the stationary surround was varied, some surround disparities produced greater modulation of MSTl neuron response than did others. Some neurons with different disparity preferences in center and surround responded best to the relative disparity differences between center and surround, whereas others were related to the absolute difference between center and surround. The combination of modulatory surrounds and the sensitivity to relative difference between center and surround disparity make these MSTl neurons particularly well suited for the segmentation of a moving object from the background.


2005 ◽  
Vol 94 (2) ◽  
pp. 1084-1090 ◽  
Author(s):  
Anne K. Churchland ◽  
Stephen G. Lisberger

We have used antidromic activation to determine the functional discharge properties of neurons that project to the frontal pursuit area (FPA) from the medial-superior temporal visual area (MST). In awake rhesus monkeys, MST neurons were considered to be activated antidromically if they emitted action potentials at fixed, short latencies after stimulation in the FPA and if the activation passed the collision test. Antidromically activated neurons ( n = 37) and a sample of the overall population of MST neurons ( n = 110) then were studied during pursuit eye movements across a dark background and during laminar motion of a large random-dot texture and optic flow expansion and contraction during fixation. Antidromically activated neurons showed direction tuning during pursuit (25/37), during laminar image motion (21/37), or both (16/37). Of 27 neurons tested with optic flow stimuli, 14 showed tuning for optic flow expansion ( n = 10) or contraction ( n = 4). There were no statistically significant differences in the response properties of the antidromically activated and control samples. Preferred directions for pursuit and laminar image motion did not show any statistically significant biases, and the preferred directions for eye versus image motion in each sample tended to be equally divided between aligned and opposed. There were small differences between the control and antidromically activated populations in preferred speeds for laminar motion and optic flow; these might have reached statistical significance with larger samples of antidromically activated neurons. We conclude that the population of MST neurons projecting to the FPA is highly diverse and quite similar to the general population of neurons in MST.


Author(s):  
Tianyi Yan ◽  
Jinglong Wu

In humans, functional imaging studies have found a homolog of the macaque motion complex, MT+, which is suggested to contain both the middle temporal (MT) and medial superior temporal (MST) areas in the ascending limb of the inferior temporal sulcus. In the macaque, the motion-sensitive MT and MST areas are adjacent in the superior temporal sulcus. Electrophysiology has identified several motion-selective regions in the superior temporal sulcus (STS) of the macaque. Two of the best-studied areas include the MT and MST areas. The MT area has strong projections to the adjacent MST area and is typically subdivided into the dorsal (MSTd) and lateral (MSTl) subregions. While MT encodes the basic elements of motion, MST has higher-order motion-processing abilities and has been implicated in the perception of both object motion and self motion. The macaque MST area has been shown to have considerably larger receptive fields than the MT area. The receptive fields of MT cells typically extend only a few degrees into the ipsilateral visual field, while MST neurons have receptive fields that extend well into the ipsilateral visual field. This study tentatively identifies these subregions as the human homologs of the macaque MT and MST areas, respectively (Fig. 1). Putative human MT and MST areas were typically located on the posterior/ventral and anterior/dorsal banks of a dorsal/posterior limb of the inferior temporal sulcus. These locations are similar to their relative positions in the macaque superior temporal sulcus.


2014 ◽  
Vol 112 (2) ◽  
pp. 353-361 ◽  
Author(s):  
Xiaodong Chen ◽  
Gregory C. DeAngelis ◽  
Dora E. Angelaki

The ventral intraparietal area (VIP) processes multisensory visual, vestibular, tactile, and auditory signals in diverse reference frames. We recently reported that visual heading signals in VIP are represented in an approximately eye-centered reference frame when measured using large-field optic flow stimuli. No VIP neuron was found to have head-centered visual heading tuning, and only a small proportion of cells had reference frames that were intermediate between eye- and head-centered. In contrast, previous studies using moving bar stimuli have reported that visual receptive fields (RFs) in VIP are head-centered for a substantial proportion of neurons. To examine whether these differences in previous findings might be due to the neuronal property examined (heading tuning vs. RF measurements) or the type of visual stimulus used (full-field optic flow vs. a single moving bar), we have quantitatively mapped visual RFs of VIP neurons using a large-field, multipatch, random-dot motion stimulus. By varying eye position relative to the head, we tested whether visual RFs in VIP are represented in head- or eye-centered reference frames. We found that the vast majority of VIP neurons have eye-centered RFs with only a single neuron classified as head-centered and a small minority classified as intermediate between eye- and head-centered. Our findings suggest that the spatial reference frames of visual responses in VIP may depend on the visual stimulation conditions used to measure RFs and might also be influenced by how attention is allocated during stimulus presentation.


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