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R Blake

Publications and source records attributed to R Blake.

At least 37 records · Page 2Linked to original sources
PubMed1997

The kinematics and performance of fish fast-start swimming

Fast-starts are brief, sudden accelerations used by fish during predator­prey encounters. The kinematics and performance of fish during fast-start manoeuvres have received a lot of attention since they may determine the outcome of predator­prey interactions in terms of feeding success or survival. We will discuss recent progress on (1) the kinematics of escape responses and feeding strikes, (2) the fast-start performance of species with different body morphologies and from different habitats, and (3) the functional significance of fast-start kinematics and performance within the context of predator­prey interactions.

Journal Article↗
PubMed1996

Stereopsis from interocular spatial frequency differences is not robust.

Based on data obtained using one-dimensional noise patterns, Tyler & Sutter (1979). (Vision Research, 19, 859-865) concluded that stereoscopic tilt can result from an interocular spatial frequency difference in the absence of consistent horizontal disparity. We tested stereopsis using two-dimensional random-dot patterns that were bandpass filtered to contain 1.0 octave bands of spatial frequency with means that differed between the two eyes. With vertical, one-dimensional stimuli we replicated the results of Tyler and Sutter. However, stereoscopic tilt was not perceived based on spatial frequency differences alone when the monocular images contained as little as a +/- 14 deg range of orientation variation. In addition, model simulations demonstrate that the modest steroscopic performance produced by interocular spatial frequency differences in one-dimensional noise patterns are predicted by random disparity correlations at the pattern edges. The observations lead to the conclusion that stereopsis from frequency differences in the absence of pointwise disparity correlations does not reflect a special processing capability of human vision but is an artifact associated with one-dimensional stimuli. As such, it plays no role in steroscopic analysis of the natural environment.

Convergence, Ocular↗
PubMed1996

Comparison of the fast-start performances of closely related, morphologically distinct threespine sticklebacks (Gasterosteus spp.)

Fast-start escape performances for two species of threespine stickleback, Gasterosteus spp., were investigated using high-speed cinematography (400 Hz). The two fishes (not yet formally described, referred to here as benthic and limnetic) inhabit different niches within Paxton Lake, British Columbia, Canada, and are recent, morphologically distinct species. All escape responses observed for both species were double-bend C-type fast-starts. There were no significant differences between the species for any linear or angular parameter (pooled averages, both species: duration 0.048 s, distance 0.033 m, maximum velocity 1.10 m s-1, maximum acceleration 137 m s-2, maximum horizontal angular velocity 473.6 rad s-1 and maximum overall angular velocity 511.1 rad s-1). Benthics and limnetics have the greatest added mass (Ma) at 0.3 and 0.6 body lengths, respectively. The maximum Ma does not include the fins for benthics, but for limnetics the dorsal and anal fins contribute greatly to the maximum Ma. The deep, posteriorly placed fins of limnetics enable them to have a fast-start performance equivalent to that of the deeper-bodied benthics. Both the limnetic and benthic fishes have significantly higher escape fast-start velocities than their ancestral form, the anadromous threespine stickleback Gasterosteus aculeatus, suggesting that the high performance of the Paxton Lake sticklebacks is an evolutionarily derived trait. In this biomechanical study of functional morphology, we demonstrate that similar high fast-start performance can be achieved by different suites of morphological characteristics and suggest that predation might be the selective force for the high escape performance in these two fishes.

Journal Article↗
PubMed1995

Syk interacts with tyrosine-phosphorylated proteins in human platelets activated by collagen and cross-linking of the Fc gamma-IIA receptor.

Activation of human platelets by cross-linking of the platelet low-affinity IgG receptor, the Fc gamma receptor IIA (Fc gamma-RIIA), or by collagen is associated with rapid phosphorylation on tyrosine of the non-receptor tyrosine kinase syk. Phosphorylation is still observed, albeit sometimes reduced, in the presence of a combination of a protein kinase C inhibitor, Ro 31-8220, and the intracellular calcium chelator, BAPTA-AM, demonstrating independence from phosphoinositide-specific phospholipase C (PLC) activity. In contrast, the combination of Ro 31-8220 and BAPTA-AM completely inhibits phosphorylation of syk in thrombin-stimulated platelets. Phosphorylation of syk increases its autophosphorylation activity measured in a kinase assay performed on syk immunoprecipitates. Fc gamma-RIIA also undergoes phosphorylation in syk immunoprecipitates from platelets activated by cross-linking of Fc gamma-RIIA but not by collagen, suggesting that it associates with the kinase. Consistent with this, tyrosine-phosphorylated Fc gamma-RIIA is precipitated by a glutathione S-transferase (GST) fusion protein containing the tandem src homology (SH2) domains of syk from Fc gamma-RIIA- but not collagen-activated cells. Two uncharacterized tyrosine-phosphorylated proteins of 40 and 65 kDa are uniquely precipitated by a GST fusion protein containing the tandem syk-SH2 domains in collagen-stimulated platelets. A peptide based on the antigen recognition activation motif (ARAM) of Fc gamma-RIIA, and phosphorylated on the two tyrosine residues found within this region, selectively binds syk from lysates of resting platelets; this interaction is not seen with a non-phosphorylated peptide. Kinase assays on Fc gamma-RIIA immunoprecipitates reveal the constitutive association of an unidentified kinase activity in resting cells which phosphorylates a 67 kDa protein. Syk is not detected in Fc gamma-RIIA immunoprecipitates from resting cells but associates with the receptor following activation and, together with Fc gamma-RIIA, is phosphorylated in the kinase assay in vitro. These results demonstrate that syk is activated by Fc gamma-RIIA cross-linking and collagen, independent of PLC, suggesting that it may have an important role in the early events associated with platelet activation. The association of syk with Fc gamma-RIIA appears to be mediated through the tandem SH2 domains in syk and the ARAM motif of Fc gamma-RIIA. A similar interaction may underlie the response to collagen, suggesting that its signalling receptor contains an ARAM motif.

Amino Acid Sequence↗
PubMed1995

Neural adaptation of imaginary visual motion.

Observers made time-to-contact judgements about an imagined moving object that passed through an area of the visual field previously adapted to a single direction of real motion. The direction of imagined motion varied relative to the direction of adapting motion. When imagined motion was in the same direction as that experienced during adaptation, imagined speed was slowed; when imagined motion was in the opposite direction, its speed was increased; when adaptation and imagined motions were orthogonal, imagined speed was unaffected. The particular influence that prior adaptation has on imagined speed suggests that imagined motion and real vision may engage common neural mechanisms without being functionally equivalent. Negative aftereffects observed in imagined motion imply that the imagination represents movement as an inference from position changes of static images.

Eye Movements↗
PubMed1995

On the accuracy of surface reconstruction from disparity interpolation.

Observers viewed flashed random-dot stereograms depicting a pair of long, narrow, curved ribbons of textured surface defined by a Gabor function in disparity. Observers judged the location of the peak of the depth profile of one ribbon relative to that of the other. In one ribbon, disparity changed smoothly while in the other disparity was periodically sampled. Up to a limiting sampling period, disparity interpolation produced accurate surface reconstruction, but beyond that performance deteriorated rapidly. This interpolation limit depended on surface orientation (vertical vs horizontal) and disparity sign, but not Gabor spatial frequency.

Depth Perception↗
PubMed1995

Discrimination of coherent motion when local motion varies in speed and direction.

Random-dot cinematograms (RDCs) consist of multiple local motion signals that can vary in direction and speed. These local motion signals can result in coherent motion: the percept of an overall direction and speed of motion in an RDC. Thresholds were obtained for discriminating differences in the strength of coherent motion. Observers were found to easily discriminate the strength of coherent motion on the basis of the elements' direction or speed under optimal conditions. However, a nonreciprocal relation was evident when this discrimination was performed under nonoptimal conditions. Discrimination of coherent motion that was based on the elements' direction was unaffected, but discrimination that was based on speed was impaired. Results indicate that humans are sensitive to small differences in coherent motion strength and suggest that the visual system processes direction and speed information nonreciprocally.

Humans↗
PubMed1995

Binocular disparity processing with opposite-contrast stimuli.

Stereoscopic perception of relative depth with reversed-contrast half images differs in several important respects from stereopsis with matched-contrast half images. Thus, reversed-contrast images show no correlated shift in visual direction, indicating that the sensory-fusion mechanism ignores opposite-sign edges; one experiment addressed this aspect of the problem. Mainly, this was a quantitative study of opposite-contrast stereopsis, in which stereoacuity was measured as a function of bar width by means of narrow-band stimuli. Acuity was about an order of magnitude worse for reversed-contrast than for matched stimuli, but the ability to see valid (disparity-dependent) depth was not altogether lost even with wide (1 cycle deg-1) reversed-contrast bars. It is generally believed that depth with opposite-contrast stimuli is mediated by interaction between binocular stimuli components that have the same sign of contrast. Perceived depth was measured as a function of disparity and thus one of the predictions of that 'same-sign hypothesis' was tested experimentally; then, the magnitude of same-sign components was manipulated within the reversed-contrast stimuli, and thus the general prediction of the same-sign hypothesis was tested. The results show conclusively that the same-sign hypothesis cannot account for opposite-contrast stereopsis; its mechanism remains unknown.

Contrast Sensitivity↗
PubMed1995

Energetic consequences of flight speeds of foraging red and hoary bats (Lasiurus borealis and Lasiurus cinereus; Chiroptera: Vespertilionidae)

We used Doppler radar readings of the flight speeds of foraging, lactating female Lasiurus borealis (N=826) and Lasiurus cinereus (N=544) to test morphologically based predictions about their flight performance. Both species flew at speeds (V=6.7 and 7.7 m s-1, respectively) that differed significantly from predicted minimum power speed (Vmp; 4.0 and 5.08 m s-1, respectively) or predicted maximum range speed (Vmr; 5.25 and 6.69 m s-1, respectively), perhaps reflecting the active pursuit of moths performing evasive manoeuvres. Estimates of costs of flight and lactation are combined with data on prey size together with encounter and capture rates to illustrate the energetic benefits accruing to these species when they forage in concentrations of insects.

Journal Article↗
PubMed1995

The mechanical power output and hydromechanical efficiency of northern pike (Esox lucius) fast-starts

The mechanical power output and hydrodynamic efficiency of northern pike, Esox lucius, during acceleration from rest (fast-start) are calculated from hydrodynamic theory for two kinematic patterns, C-starts (used in escape) and S-starts (used in prey capture). The Weihs model is employed and modified to calculate the mechanical power produced by a fish during a fast-start. A term is included for the power required to accelerate body sections laterally. Lateral deceleration of fish body sections and their associated added mass are expressed as an active process requiring energy expenditure or as a passive process requiring no energy expenditure. In addition, two methods of calculating useful power (the power used to accelerate the virtual mass of the fish, i.e. fish body mass + longitudinal added mass, in the direction of motion), one derived from the Weihs model and the second by summing the changes in kinetic energy of the virtual mass of the fish during a fast-start, are compared and found to give similar estimates of useful power (not significantly different; differences average 22 %). Comparisons of the kinematics and performance of C- and S-starts reveal that C-starts are consistently terminated after two tail flips (stages 1 and 2) whereas S-starts continue for 3­6 tail flips (stages 3­6). In addition, acceleration during C-starts is more rapid and velocities are higher (2.3­2.8 m s-1) than during S-starts (0.8­1.8 m s-1) over the first 100 ms. However, the peak velocities achieved during S-starts and C-starts are similar over the duration of a fast-start. The superior acceleration rates achieved during the initial stages of a C-start can be explained, in part, by the use of greater maximum angles of attack, higher lateral and perpendicular velocities and larger maximum forces by the caudal fin. Hydrodynamic efficiencies for fast-starts range from 0.16 to 0.39, values that are lower than those observed during either burst-and-coast or steady swimming. Efficiencies are lower for S-starts than for C-starts during the first two tail beats. S-start efficiencies increase with each subsequent tail flip and the maximum efficiencies realised are similar to those achieved during C-starts. Power output during C- and S-starts (449.0 and 394.9 W kg-1 muscle fibre, respectively) approaches the theoretical maximum for vertebrate striated muscle (500 W kg-1). Also, the inferred muscle stress is close to the predicted optimum for maximum power output, at 30 % of the maximum isometric stress recorded for isolated fast muscle fibres. These measurements suggest that fast-start performance is near a physiological limit and is probably constrained by muscle function. The superior acceleration rates achieved by C-starts over S-starts are explained in part by differences in hydrodynamic efficiency, whereas power outputs are similar.

Journal Article↗
PubMed1994

Broad tuning for spatial frequency of neural mechanisms underlying visual perception of coherent motion.

Neural events underlying perception of coherent motion are generally believed to be hierarchical: information about local motion is registered by spatio-temporal coincidence detectors whose outputs are cooperatively integrated at a subsequent stage. There is disagreement, however, concerning the spatial scale of the neural filters underlying these operations. According to one class of models, motion registration is initially accomplished in parallel at multiple spatial scales, with filters tuned to lower spatial frequencies responsive to larger motion displacements than filters tuned to higher frequencies. According to another scheme, motion analysis involves a single, broadly tuned spatial filter, with optimal displacement dependent on spacing of local elements. Here we use a masking procedure to measure the extent to which dynamic noise depicted at one spatial scale interferes with detection of coherent motion conveyed by image features at another spatial scale. Our results indicate that a single filter, broadly tuned for spatial frequency, is mediating detection of coherent motion. This finding dovetails with known physiological properties of neurons at an intermediate stage of motion processing.

Fourier Analysis↗
PubMed1994

Gibson's inspired but latent prelude to visual motion perception.

Gibson's 1954 article is paradoxical: This forward-looking review of visual motion perception anticipates developments in the field, yet those developments were achieved without closely following Gibson's footsteps. This commentary offers several possible reasons for the dormancy of Gibson's ideas about motion perception and evaluates contemporary work on motion perception in the context of Gibson's perspective.

History, 20th Century↗
PubMed1994

Binocular rivalry disrupts stereopsis.

Does the shift from binocular rivalry to fusion or stereopsis take time? We measured stereoacuity after rivalry suppression of one half-image of a stereoacuity line target. After the observer signalled that the single stereo half-image had been suppressed, the other half-image was presented for a variable duration. Stereoacuity thresholds were elevated for 150-200 ms. A control experiment demonstrated that the threshold elevation was due to rivalry suppression per se, rather than masking effects associated with the rivalry-inducing target. Monocular Vernier thresholds, measured as the smallest identifiable abrupt shift in the upper line of an aligned Vernier target that had previously been suppressed by rivalry, were elevated for a much longer duration. This result shows that an appropriately matched stereo pair can break rivalry suppression more easily than can monocular changes in position. With the aid of a similar paradigm, we also measured the duration needed to detect a disparate feature in a random-dot stereogram after rivalry suppression of one half-image of the stereogram. Observers could correctly identify the location of the disparate feature (upper or lower visual field) when the other half-image was presented for a duration ranging from 150-650 ms. In the absence of the matching half-image, the first half-image was suppressed by the rival target for a far longer duration (a few seconds). These findings show that although stereopsis and fusion terminate rivalry, both are initially disrupted for a few hundred milliseconds by rivalry suppression.

Depth Perception↗
PubMed1994

Binocular rivalry and fusion under scotopic luminances.

A study is reported of human binocular rivalry and fusion over a range of luminances from scotopic to photopic. At scotopic light levels, rivalry alternations were very slow and complete. Suppression spread over much larger areas of the visual field than at photopic light levels. As luminances decreased from photopic to scotopic levels there was a rod-cone break for binocular rivalry. Mean suppression durations became abruptly greater as light levels dropped below those allowing the cones to be active. Horizontal disparities allowing fusion were 4 to 6 times greater at scotopic than at photopic light levels. Binocular vision at scotopic luminances was sluggish and of low resolution. It is as though connections to, and within, binocular vision are changed when light levels allow only rod input.

Adult↗
PubMed1994

Interocular transfer of expansion, rotation, and translation motion aftereffects.

The motion aftereffect demonstrates the existence of direction-selective mechanisms in the visual system. However, direction-selective cells exist within many visual areas, including V1 and MT/V5. Can motion aftereffects be generated within each of these areas? In visual cortical areas beyond V1 almost all cells are binocular, whereas a smaller percentage are binocular in V1. The degree of binocularity can be revealed psychophysically by assessing interocular transfer. Interocular transfer of motion aftereffects generated from expanding rotating, and translating dynamic random-dot patterns were therefore compared, since these stimuli should activate cells in higher visual areas selectively. Partial interocular transfer was found that was greater for expansion and rotation than for translation. The results support the involvement of higher visual areas in motion aftereffects to complex animation sequences.

Female↗
PubMed1993

Visually guided attention is neutralized when informative cues are visible but unperceived.

The ability to voluntarily shift the focus of visual attention away from the focus of gaze was investigated in a novel paradigm designed to elaborate the stages of processing underlying this ability. A basic experimental method used to investigate guided visual attention involves measuring response times to targets presented at positions of which the observer has been informed by an orienting cue. Binocular rivalry was utilized to dissociate presentation of the orienting cue from visual awareness of that cue. The findings indicated that when an informative cue was presented to an eye during the dominance phase, thus reaching visual awareness, manual response times were significantly affected by cue validity. In contrast, when the same cue was presented to an eye during suppression, and thus was not seen by observers, response times were not influenced by cue validity. We conclude that to guide attention, neural signals registering informative visual cues must be processed at stages lying beyond the site of rivalry suppression. Implications for investigating the neural basis of visual attention are discussed.

Attention↗