Workplace health beliefs concerning physical activity and sedentary behaviour.

BACKGROUND: Sedentary behaviour (SB) in the form of uninterrupted sitting constitutes a risk factor for chronic disease that is independent of the risks associated with insufficient physical activity (PA). However, little is known about employee and manager health beliefs concerning SB and PA. AIMS: We assess health beliefs of desk-based workers concerning PA and SB accrued at work versus during leisure. We ask whether recreational PA attenuates the perceived ill-health effects of prolonged occupational SB, and compare attitudes of employees and managers to interventions aimed at reducing/interrupting workplace sitting. METHODS: Two hundred and twenty-two desk-based employees and 121 managers located in Melbourne, Australia, rated the healthiness of vignettes describing combinations of uninterrupted sitting, sitting with breaks, light PA and moderate-to-vigorous PA accumulated at work and during leisure time. Participants also responded to open-ended questions concerning the implications of reducing workplace sitting. RESULTS: Mixed-model ANOVA revealed that the presence of leisure-time PA greatly diminished the perceived detrimental effects to health of workplace sitting. Subsequent thematic analysis of qualitative data further revealed that participants' concerns with SB were primarily musculoskeletal and workplace performance rather than chronic health. CONCLUSIONS: Employees and their managers do not rate uninterrupted sitting as being unhealthy when it is presented to them in the form of an 'active couch potato' lifestyle (a person who meets minimum PA recommendations but spends much of their work time and non-PA time sitting). We recommend that interventions targeting workplace SB take into account the contextual nature of health beliefs.

Adaptation reveals a neural code for the visual location of orientation change.

We apply an adaptation technique to explore the neural code for the visual location of textures defined by modulation of orientation over space. In showing that adaptation to textures modulated around one orientation shifts the perceived location of textures modulated around a different orientation, we demonstrate the existence of a neural code for the location of orientation change that generalises across orientation content. Using competitive adaptation, we characterise the neural processes underlying this code as single-opponent for orientation, that is with concentric excitatory/inhibitory receptive areas tuned to a single orientation.

Orientation integration in detection and discrimination of contrast-modulated patterns.

Orientation detection and discrimination thresholds were measured for Gabor 'envelopes' formed from contrast-modulation of luminance 'carriers'. Consistent with previous research differences between carrier and envelope orientation had no effect on sensitivity to envelopes. Using plaid carriers in which the proportion of contrast modulation 'carried' by each plaid component was systematically manipulated, it was shown that this tolerance to carrier-envelope orientation difference reflects linear summation across orientation indicative of a single second-stage channel coding for contrast-defined structure. That contrast envelopes did not exhibit linear summation across spatial-frequency, nor across combinations of orientation and spatial-frequency differences, suggests that these second-order channels operate only within certain spatial scales. Using arrays of Gabor micropatterns as carriers in which the orientation distribution of the carriers was manipulated independently of the difference between envelope orientation and mean carrier orientation, it was further demonstrated that the locus of orientation integration must occur prior to envelope detection. In the context of two-stage models that incorporate a non-linearity between the stages, the pattern of results obtained is consistent with the operation of an orientation pooling process between first-stage and second-stage channels, analogous to having all filters of the first-stage feed into all filters of the second-stage within the same spatial-frequency band.

Alignment of orientation-modulated textures.

We conducted a Vernier acuity experiment using orientation-modulated (OM) textures in which the overall shape (skewness) of the modulations was manipulated independently of their orientation content. Misalignments between OMs were consistent with the application of global positional tags, but not on the basis of a single cue (e.g. centroid, peak, or zero-crossing). Instead, modelling of our results in terms of orientation-opponent spatial filters not only led to an excellent fit, but also to estimates of the size and shape of these filters that correspond closely to those made by other researchers using a different task and different stimulus parameters and configurations.

Amblyopic deficits in detecting a dotted line in noise.

We compared detectability of a dotted line masked by random-dot noise for the amblyopic versus non-amblyopic eye of two strabismic amblyopes. Small but consistent deficits in the amblyopic eye of these observers were found, and shown to be limited to dotted-line targets composed of greater than seven dots (with performance being normal for targets of less than seven dots). These deficits were unrelated to impaired visual acuity, impaired sensitivity to dot density, and differential positional uncertainty between the eyes of our observers. The deficits were also unlikely to be due to CSF losses due to abnormal low-spatial-frequency filters involved in detecting long chains of collinear dots. Instead, the results of simulations indicate that the inefficiency in utilising large numbers of dots is due to deficits of global, integrative processes in strabismic amblyopes. These simulations also show that while neither undersampling nor positional uncertainty of inputs into integrative processes can themselves account for the amblyopic deficits, if such abnormal inputs lead to the development of stunted integrative processes then impaired sensitivity to long chains of collinear dots is indeed predicted.

Orientation-based texture segmentation in strabismic amblyopia.

Texture segmentation of 'target' Gabors from an array of 'background' Gabors was measured in terms of the difference in orientation between the two regions, as well as the difference in orientation within each region. Segmentation was shown to occur on the basis of local orientation differences at the boundary between the target and background regions (Nothdurft, H.C. (1992). Feature analysis and the role of similarity in preattentive vision. Perception and Psychophysics, 52, 355-375.). We obtained similar results for both the amblyopic and non-amblyopic eye of three strabismic amblyopes, and showed also that the effects of texture undersampling and positional jitter were similar for the two eyes. This pattern of results is consistent with intact mechanisms of texture perception in amblyopic cortex, and suggests also that any amblyopic deficits in first-order cortical units (undersampling and/or positional uncertainty) do not limit higher-order texture segmentation processes. Therefore, first- and second-order processes involved in perceptual grouping of oriented elements (that appear to be abnormal in amblyopic cortex; Kovács, I., Polat, U., Norcia, A.M. (1996). Breakdown of binding mechanisms in amblyopia. Association for Research in Vision and Ophthalmology Abstracts; Mussap, A.J., Levi, D.M. (1995). Amblyopic deficits in perception of second-order orientation. Investigative Ophthalmology and Visual Science (Supplement), 36, S634; Mussap, A.J., Levi, D.M. (1998). Amblyopic deficits in perceptual grouping. Vision Research, submitted) do not contribute to texture perception based on orientation contrast.

Detecting collinear dots in noise.

We estimated the sensitivity for detecting a row of collinear target elements (usually dots) by measuring the maximum density of randomly positioned noise elements that allowed 75% correct detection of the orientation of alignment (binary choice: horizontal versus vertical) of the target elements. We varied the number of target elements, their mode of generation, and their accuracy of positioning. As reported previously (Moulden (1994) Higher-order processing in the visual system. Ciba Foundation Symposium 184. Chichester: Wiley), target detection improved rapidly until the number of target elements reached about seven, and then improved more slowly beyond this point. However, this break was reduced (and often removed entirely) when the target array was formed by repositioning pre-existing noise elements lying close to the target location, rather than by superimposition of additional target elements onto the noise array. This almost linear slope of improvement, coupled with the observation that target detection was disrupted more by random jitter of target elements at right angles to their axis of alignment than by jittering along this axis, argues against a two-stage process of perceptual grouping (Moulden, 1994) and supports instead an explanation based on the operation of a single mechanism. This single mechanism explanation is further supported by the observation that intrinsic positional uncertainty (estimated from the results of jitter experiments) was independent of target element number. Additional experiments showed that target detection is facilitated by aperiodic noise dots that fall close to the target axis. The results are discussed in relation to alternative explanations of perceptual grouping.

Directions of motion after-effects induced by gratings and plaids.

In three experiments the direction of motion after-effect (MAE) is measured following adaptation to two gratings moving in different directions presented in alternation (component-induced MAEs: CMAEs), and to moving plaid patterns composed of superimposed pairs of these gratings (plaid-induced MAEs; PMAEs). These MAEs are compared to: (i) the vector sum direction of the component gratings; (ii) the IOC-predicted direction of the plaids; and (iii) the perceived direction of the plaids as reported by observers. Contrary to previous findings (Burke D, Wenderoth P. Vis Res 1993;33:351-9), directions of PMAEs are shown to approximate the vector sum direction of the components, whereas directions of CMAEs are shown to approximate the mean (unweighted) direction of the components. This difference is attributed to the activity, and adaptation, of an additional population of neurones whose stimulus), or a counterphase moving plaid (a combined Fourier and non-Fourier stimulus), rules out the possibility that the discrepancy between PMAE direction and actual plaid direction is due to the use of test stimuli that do not adequately reflect adaptation by the Fourier and non-Fourier components of the adapting plaids (HR, Ferrera VP, Yo C. Vis Neurosci 1992;9:79-97). Various explanations of this paradoxical result are discussed, including: (i) that MAEs produced by Fourier components out-weigh (and possibly even mask) MAEs produced by non-Fourier plaid components; (ii) PMAEs are influenced by adaptation of a population of component-selective neurones that do not contribute to plaid perception; and, (iii) PMAEs are influenced by component-specific adaptation effects that are weighted according to relative component sensitivity, rather than relative component speed (Pantle A. Vis Res 14;1974:1229-36). We review psychophysical and neurophysiological evidence consistent with these explanations.

Vernier acuity with plaid masks: the role of oriented filters in vernier acuity.

Superimposition of oriented grating masks on vernier targets results in bimodal patterns of vernier threshold elevation, with peaks occurring on either side of vernier target orientation. These bimodal masking effects suggest a contribution to vernier acuity from spatial filters tuned to orientations on either side of the target. We report similar bimodal threshold elevation with plaid masks composed of symmetrically oriented pairs of gratings. Since filters oriented to either side of the vernier stimulus will be affected similarly by plaid masks, it is unlikely that threshold elevation reflects disruption of relative filter activity that is used to code for change in target orientation. Instead, the results support the proposition that misalignments are detected on the basis of differential (i.e. absolute rather than relative) activity of spatial filters. Our plaid-mask data also rule out the possibility that: (i) "off-channel" looking; or (ii) detection of orientation shifts (e.g. tilt illusions), underlie bimodal masking effects. The finding that weak bimodal threshold elevation occurs with dot targets separated by 40 min arc further suggests that the mechanisms involved in detecting misalignments over large regions [possibly collator/collector-type mechanisms] also do so via analysis of their differential activity.

The influence of aperture surfaces on the barber-pole illusion.

The magnitude of the barber-pole illusion is measured as a function of the contrast, orientation, and phase difference between the moving 'barber-pole' grating and a moving 'surround' grating that forms the aperture surface. It is found that as the difference between the barber-pole grating and the surround grating increases, the influence of surround motion on barber-pole motion decreases (resulting in an increase in the magnitude of the barber-pole illusion). This pattern of results is interpreted as evidence for competition between processes that detect the motion of line terminators along the length of the rectangular aperture and processes that detect grating motion in directions perpendicular to grating orientation.

Spatial properties of filters underlying vernier acuity revealed by masking: evidence for collator mechanisms.

Models of vernier acuity based on the differential response of oriented filters receive support from the finding that vernier threshold elevation peaks for grating mask orientations which are slightly different from the orientation of the vernier bars. We replicate this effect using long, abutting vernier bars, and masks which possess gaps up to 22.5' wide (Experiments 1 and 3); a surprising result considering that vernier acuity improves little for bars longer than 10'. To account for this we suggest the involvement of elongated mechanisms (referred to as collators or collectors) that "integrate" responses of numerous smaller filters along the axis of their common orientation. The collator model explains patterns of threshold elevation obtained with a variety of mask-vernier configurations. In particular, the model predicts that masks located midway between separated vernier bars will interfere with integrative processes occurring over the entire region encompassing both bars (Experiment 2). In confirmation of this prediction we find that centrally placed masks produce significant orientation-specific threshold elevation. In suggesting a contribution to vernier acuity from integrative mechanisms, our results, along with others, emphasize the importance of global processes in vernier acuity.

Binocular processes in vernier acuity.

We investigate the role of binocular mechanisms in vernier acuity, using dichoptic variants of spatial-frequency masking and flank-line interference paradigms. The finding that grating masks and flanking lines presented to one eye elevate (worsen) thresholds for detecting vernier offsets presented to the other eye suggests that neural mechanisms mediating vernier acuity receive binocular inputs, thus placing the loci of these mechanisms at postreceptoral sites. The observation that these threshold elevation effects are orientation dependent is consistent with a contribution to vernier acuity from oriented cortical filters.

Amodal completion and vernier acuity: evidence of 'top-but-not-very-far-down' processes?

Vernier thresholds were measured by means of a forced-choice paradigm for physically separated bars that were perceived either as separate or as amodally completed behind an occluder. The finding that thresholds were not reduced (improved) with amodal completion argues against an early neural code for amodal completion that is equivalent to physical completion of the vernier bars (ie neural propagation/interpolation) and limits the stage at which amodal representations could arise via bottom-up processes to neural sites located centrally with respect to those involved in position coding. An alternative explanation is also considered, that this result reflects the activity of top-down processes that mediate amodal completion by imposing grouping/organizational constraints upon earlier representations of position. In support of this proposition it was found that when tested by means of a non-forced-choice paradigm without feedback, observers demonstrated a reduced tendency to report the presence of a vernier offset when the bars were perceived as amodally completed (ie a shift in response bias occurred). This separability of vernier acuity and response bias suggests the existence of 'top-but-not-very-far-down' grouping processes whose influence does not extend to early representations of relative position.

Barber-pole illusions and plaids: the influence of aperture shape on motion perception.

The barber-pole illusion and its influence on plaid perception were investigated in two experiments to test the following expectations: (i) apertures which bias the perception of grating motion in directions consistent with plaid direction will facilitate plaid perception, and (ii) apertures which bias the perception of grating motion in directions inconsistent with plaid direction will disrupt plaid perception. In experiment 1 the barber-pole illusion was measured as a function of grating orientation (20 degrees, 45 degrees, and 70 degrees, clockwise and counterclockwise from horizontal), and aperture shape (vertical, horizontal; at each of three elongations). Barber-pole illusions reported with 45 degrees gratings increased with increased aperture elongation. However, this was not found with 20 degrees and 70 degrees gratings; these were almost always reported as moving in a direction parallel to the side of the aperture with which the gratings formed angles approaching 90 degrees. In experiment 2 this dependence of barber-pole illusions on the relative orientation between gratings and apertures was also evident with 45 degrees gratings in oblique apertures; only oblique directions of grating motion were reported. The influence of the same apertures on the separate contrast thresholds required for initial plaid coherence and initial plaid decomposition was measured. In experiments 1 and 2, coherence thresholds were unaffected by apertures, contrary to expectation (i). However, in both experiments expectation (ii) was confirmed; decomposition thresholds decreased in apertures which biased perceived direction of gratings towards vertical (plaid direction), and increased in apertures which biased grating motion away from vertical. Adaptation of plaid mechanisms during measurement of decomposition thresholds was proposed to explain the discrepancy between coherence and decomposition data. Taken together, the results were interpreted as reflecting interactions between mechanisms mediating the barber-pole illusion and mechanisms mediating plaid perception.