The two experiments demonstrated that consistent with Bleumers et al. (
2008), the grouping task with peripherally presented dot lattices produces random guesses in a proportion of trials. However, the present results cannot be explained by stimulus-independent lapses of attention. Both experiments show that the probability of random responses is strongly affected by the
b/
a ratio and type of lattice. It seems that with peripheral presentation, grouping performance is limited by some kind of noise that masks relatively weak and ambiguous orientation signals while the
b/
a ratio is close to 1. With increasing
b/
a ratios, not only the relative but also absolute strength of a dominant orientation signal probably increases, making the grouping along that orientation visible within the noise. The characteristic differences between the two lattice types suggest that a simple positional noise might play a role in these results. A close look at the lattices used in this study reveals that regardless of the same minimal inter-dot distance and the same
b/
a ratio, the triangular lattices have smaller average distances between the dots. Consequently, adding the same 2D noise to the positions of the dots must distort this lattice more severely. In addition, several studies have reported spatial uncertainty as an important property of peripheral vision and measured internal positional noise at different eccentricities (e.g., Hess & Dakin,
1999; Hess & Hayes,
1994; Levi, Klein, & Aitsebaomo,
1985).
If the random responses with peripheral presentation are caused by internal positional noise, then it should be possible to produce similar results by adding external noise to centrally presented stimuli. I tested this prediction in a supplementary experiment. The methods were identical to those of Experiment 2, except the lattice was presented at the fixation point and Gaussian noise (
SD 3 pixels) was added to the
x and
y coordinates of each dot. Examples of stimuli are given in
Figure 7. Two observers participated in the experiment (600 trials).
Figure 7 depicts the proportions of random responses, estimated in the same way as in Experiment 2. The pattern of results is really similar to those of Experiment 2. Both observers exhibit a decreasing proportion of random responses with increasing
b/
a ratios and a higher proportion of random responses with triangular lattices. Thus, the results show that adding positional noise to the dots of a centrally presented lattice produces the same effects as presenting a noiseless lattice in the visual periphery. This is strong support for the hypothesis that internal positional noise in the visual periphery might be the main cause of the central–peripheral differences in proximity grouping.
Finally, I attempted to build a simple computational model (
Figure 8) that could take the images of dot lattices as input and produce response distributions similar to those found in the experiments. I used a set of spatial filters tuned to 16 different orientations (evenly distributed, step 11.25 deg) and 9 wavelengths (from 4 to 12 pixels). The filters had symmetrical (cosine phase) Gabor profiles with circular Gaussian window (standard deviation equal to the wavelength). Spatially, the filters were positioned at the center of a lattice. The size of images was 63 × 63 pixels, and the minimal distance between dots was 8 pixels. Pixel values were 1 for the dots and 0 for background. The model calculated the filter responses (weighted sum, dot product) to a given lattice and added independent Gaussian noise (standard deviation 2) to the results. (Without that noise, the model would always choose the same response when the same noise-free lattice is presented.) The filter with maximum response was selected, and its orientation was used as the model's response in a given trial. I generated simulation results for the lattices of different types, with different
b/
a ratios, with and without positional noise (300 simulated trials per condition). For a better comparability with the experimental data, I convolved the response distributions with a typical distribution of human orientation errors (
SD 10 deg) and presented the results in 8 orientation categories.
The results (see
Figure 8) show that this simple model reproduces virtually all qualitative regularities of the human data. The simulated data without positional noise are well in accord with PDL (
p > 0.9). With positional noise, the estimated proportions of random responses follow the same pattern as observed in the experiments with human observers exposed to the similar noisy stimuli, or when noiseless stimuli are presented in the visual periphery. Thus, the simulation provides an additional support to the idea that positional noise can produce the results that are observed in experiments with peripheral presentation of dot lattices.
The results of the present study look a bit different from Bleumers et al.'s (
2008) conclusions. These authors claimed that stimulus-independent random guesses could explain their results from peripheral presentation. There are several reasons why it could be difficult to observe the effect of
b/
a ratio on the probability of random responses in that study. They varied
b/
a ratio over a relatively small range (from 1 to 1.26). Their lattices were somewhat larger (relative to eccentricity) and exposure duration was longer, which should reduce the total amount of random responses. They did not use tri-stable lattices that produced the largest proportion of random responses in the present study. In addition, note that only using response alternatives far from dominant grouping orientations (as in the present study) allows a robust estimation of the probability of random responses. However, it is not impossible that their procedure really produced stimulus-independent lapses of attention on some proportion of trials. (I reanalyzed their results and found a significant decrease of random responses with increasing
b/
a ratios at 15-deg eccentricity in their Experiment 1 but not in Experiment 2.)
In this study, I followed Bleumers et al.'s (
2008) idea that deviation from PDL in the visual periphery can be explained by random guessing in a proportion of trials. An alternative possibility of increased orientation errors looks less likely. Supposedly, the orientation errors are introduced at relatively late stages after the grouping and seem to be independent of
b/
a ratio and lattice type (Kubovy et al.,
1998). In addition, I have found that using variable
SD of orientation errors could not fit the present data as well as variable proportions of random responses.
Although I used the PDL (Kubovy et al.,
1998) as a kind of baseline model, the results of the present study do not favor this or any other specific function used to quantify proximity grouping. However, the present findings point at some limitations of Kubovy et al.'s (
1998) assumption that relative inter-dot distances along different orientations solely determine the probabilities of perception of differently oriented groupings while the angles between orientations (or lattice types) do not matter. This seems to be correct for central noiseless presentation but not for peripheral presentation or for lattices with positional noise. The simulations run in the present study indicate that it is possible to build a biologically plausible computational model of proximity grouping that reproduces the regularities reported in previous studies (e.g., Kubovy et al.,
1998; Kubovy & Wagemans,
1995) and also accounts for the effects of (internal or external) positional noise.