Saccadic latency in amblyopia.

We measured saccadic latencies in a large sample (total n = 459) of individuals with amblyopia or risk factors for amblyopia, e.g., strabismus or anisometropia, and normal control subjects. We presented an easily visible target randomly to the left or right, 3.5° from fixation. The interocular difference in saccadic latency is highly correlated with the interocular difference in LogMAR (Snellen) acuity-as the acuity difference increases, so does the latency difference. Strabismic and strabismic-anisometropic amblyopes have, on average, a larger difference between their eyes in LogMAR acuity than anisometropic amblyopes and thus their interocular latency difference is, on average, significantly larger than anisometropic amblyopes. Despite its relation to LogMAR acuity, the longer latency in strabismic amblyopes cannot be attributed either to poor resolution or to reduced contrast sensitivity, because their interocular differences in grating acuity and in contrast sensitivity are roughly the same as for anisometropic amblyopes. The correlation between LogMAR acuity and saccadic latency arises because of the confluence of two separable effects in the strabismic amblyopic eye-poor letter recognition impairs LogMAR acuity while an intrinsic sluggishness delays reaction time. We speculate that the frequent microsaccades and the accompanying attentional shifts, made while strabismic amblyopes struggle to maintain fixation with their amblyopic eyes, result in all types of reactions being irreducibly delayed

Additivity of the Renyi entropy of order 2 for positive-partial-transpose-inducing channels

We prove that the minimal Renyi entropy of order 2 (RE2) output of a positive-partial-transpose(PPT)-inducing channel joint to an arbitrary other channel is equal to the sum of the minimal RE2 output of the individual channels. PPT-inducing channels are channels with a Choi matrix which is bound entangled or separable. The techniques used can be easily recycled to prove additivity for some non-PPT-inducing channels such as the depolarizing and transpose depolarizing channels, though not all known additive channels. We explicitly make the calculations for generalized Werner-Holevo channels as an example of both the scope and limitations of our techniques.Comment: 4 page

Orientation of Listing’s plane during static tilt in young and older human subjects

AbstractThree-dimensional eye positions, when expressed as rotation vectors, are constrained to lie in a head-fixed Listing’s plane. The offset and orientation of Listing’s plane changes when the head is tilted. To assess the influence of age on this phenomenon, young (less than 30 years old) and older (>65 years old) human subjects were seated upright, pitched nose up and nose down, and rolled right ear down and left ear down. Listing’s plane was computed from eye movements recorded using a dual scleral search coil while subjects scanned a complex visual scene. During pitch, Listing’s plane counterpitched with respect to the head, while during roll, it translated in a manner consistent with “ocular counterrolling”. There was no significant difference in this reorientation of Listing’s plane between the young and older subjects. The only obvious difference between the two age groups was that the “thickness” of Listing’s plane was greater in the older subjects. This suggests that aging has a small, but definite, influence on Listing’s law

Unconstrained stereoscopic matching of lines

The computation of horizontal binocular disparities used in stereoscopic depth perception depends upon the identification of corresponding features in the two retinal images. In principle, binocular matching is a two-dimensional problem that considers matches in all possible meridians. Normally, constraints such as end points or crossing points limit the direction and magnitude of matches. If matching is unconstrained, such as is the case with long lines, it is completely ambiguous. Under these conditions the default match will be determined by the operating range, or upper disparity limit, of matchable vertical and horizontal disparities. We computed the operating range of vertical matches for stereoscopic depth as a function of line orientation. Our results suggest that the two-dimensional operating range is anisotropic for vertical and horizontal disparity and that unconstrained matches are not based upon either epipolar geometry or nearest neighbor constraints, but rather the mean of disparity estimates within the operating range for binocular matches. This operating range can be extended vertically when matches are constrained by image primitives

Initial destination of the disaccommodation step response

AbstractPeak velocity and peak acceleration of disaccommodation step responses remain invariant of response magnitude for a constant starting position and they increase linearly with proximity of starting position. This suggests that disaccommodation response is initiated towards an initial (default) destination and is switched mid-flight to attain the desired final destination. The dioptric location of initial destination was estimated from the x-intercept of regression of peak velocity on response starting position. The x-intercept correlated well with subject’s cycloplegic refractive state and poorly with their dark focus of accommodation. Altering the dark focus by inducing fatigue in the accommodative system did not alter the x-intercept. These observations suggest that cycloplegic refractive state is a good behavioral correlate of initial destination of disaccommodation step responses

Context-specific adaptation of vertical vergence to correlates of eye position

AbstractVertical phoria (vertical vergence in the absence of binocular feedback) can be trained to vary with non-visual cues such as vertical conjugate eye position, horizontal conjugate eye position and horizontal vergence. These prior studies demonstrated a low-level association or coupling between vertical vergence and several oculomotor cues. As a test of the potential independence of multiple eye-position cues for vertical vergence, context-specific adaptation experiments were conducted in three orthogonal adapting planes (midsagittal, frontoparallel, and transverse). Four vertical disparities in each of these planes were associated with various combinations of two specific components of eye position. Vertical disparities in the midsagittal plane were associated with horizontal vergence and vertical conjugate eye position; vertical disparities in the frontoparallel plane were associated with horizontal and vertical conjugate eye position; and vertical disparities in the transverse plane were associated with horizontal vergence and horizontal conjugate eye position. The results demonstrate that vertical vergence can be adapted to respond to specific combinations of two different sources of eye-position information. The results are modeled with an association matrix whose inputs are two classes of eye position and whose weighted output is vertical vergence

Human stereo matching is not restricted to epipolar lines

AbstractComputational approaches to stereo matching have often taken advantage of a geometric constraint which states that matching elements in the left and right eye images will always fall on “epipolar lines”. The use of this epipolar constraint reduces the search space from two dimensions to one, producing a tremendous saving in the computation time required to find the matching solution. Use of this constraint requires a precise knowledge of the relative horizontal, vertical and torsional positions of the two eyes, however, and this information may be unavailable in many situations. Experiments with dynamic random element stereograms reveal that human stereopsis can detect and identify the depth of matches over a range of both vertical and horizontal disparity. Observers were able to make accurate near/far depth discriminations when vertical disparity was as large as 45 arcmin, and were able to detect the presence of correlation over a slightly larger range. Thus, human binocular matching sensitivity is not strictly constrained to epipolar lines

Short-term adaptation of accommodation, accommodative vergence and disparity vergence facility

AbstractPrevious studies have found that subjects can increase the velocity of accommodation using visual exercises such as pencil push ups, flippers, Brock strings and the like and myriad papers have shown improvement in accommodation facility (speed) and sufficiency (amplitude) using subjective tests following vision training but few have objectively measured accommodation before and after training in either normal subjects or in patients diagnosed with accommodative infacility (abnormally slow dynamics). Accommodation is driven either directly by blur or indirectly by way of neural crosslinks from the vergence system. Until now, no study has objectively measured both accommodation and accommodative–vergence before and after vision training and the role vergence might play in modifying the speed of accommodation. In the present study, accommodation and accommodative–vergence were measured with a Purkinje Eye Tracker/optometer before and after normal subjects trained in a flipper-like task in which the stimulus stepped between 0 and 2.5diopters and back for over 200 cycles. Most subjects increased their speed of accommodation as well as their speed of accommodative vergence. Accommodative vergence led the accommodation response by approximately 77ms before training and 100ms after training and the vergence lead was most prominent in subjects with high accommodation and vergence velocities and the vergence leads tended to increase in conjunction with increases in accommodation velocity. We surmise that volitional vergence may help increase accommodation velocity by way of vergence–accommodation cross links

Stimulation by a low-molecular-weight angiogenic factor of capillary endothelial cells in culture.

A low-mol.-wt compound isolated from rat Walker 256 carcinoma and found to induce neovascularization in vivo was tested on cultures of cow brain-derived endothelial cells (CBEC) growing on plastic and collagen substrates. This factor had a mitogenic effect on CBEC cultured on native collagen gels and for this reason has been called "endothelial-cell-stimulating angiogenesis factor" (ESAF). CBEC growing on plastic culture dishes or denatured collagen films were not stimulated by ESAF. The mitogenic effect of ESAF was equally apparent when added to cells already attached to the native collagen substrate or when the collagen substrate was pre-incubated with ESAF before plating the cells. A floating collagen gel pre-incubated with ESAF in cultures of CBEC growing on plastic dishes did not stimulate cell growth. Our data indicate that the substrate influences cell behaviour and that CBEC only respond to ESAF when growing on a native collagen substrate

Disparity-driven vs blur-driven models of accommodation and convergence in binocular vision and intermittent strabismus

Background. Current models of concomitant, intermittent strabismus, heterophoria, convergence and accommodation anomalies are either theoretically complex or incomplete. We propose an alternative and more practical way to conceptualize clinical patterns. Methods. In each of three hypothetical scenarios (normal; high AC/A and low CA/C ratios; low AC/A and high CA/C ratios) there can be a disparity-biased or blur-biased “style”, despite identical ratios. We calculated a disparity bias index (DBI) to reflect these biases. We suggest how clinical patterns fit these scenarios and provide early objective data from small illustrative clinical groups. Results. Normal adults and children showed disparity bias (adult DBI 0.43 (95%CI 0.50-0.36), child DBI 0.20 (95%CI 0.31-0.07) (p=0.001). Accommodative esotropes showed less disparity-bias (DBI 0.03). In the high AC/A and low CA/C scenario, early presbyopes had mean DBI of 0.17 (95%CI 0.28-0.06), compared to DBI of -0.31 in convergence excess esotropes. In the low AC/A and high CA/C scenario near exotropes had mean DBI of 0.27, while we predict that non-strabismic, non-amblyopic hyperopes with good vision without spectacles will show lower DBIs. Disparity bias ranged between 1.25 and -1.67. Conclusions. Establishing disparity or blur bias, together with knowing whether convergence to target demand exceeds accommodation or vice versa explains clinical patterns more effectively than AC/A and CA/C ratios alone. Excessive bias or inflexibility in near-cue use increases risk of clinical problems. We suggest clinicians look carefully at details of accommodation and convergence changes induced by lenses, dissociation and prisms and use these to plan treatment in relation to the model