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Bernal S D_2010.pdf - University of Plymouth

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6.1. ANALYSIS OF RESULTS<br />

over lime. The fact the both the bottom and lop layers are clamped means that beliefs can<br />

only evolve freely along Ihe intermediate layers, as the belief in peripheral layers will he<br />

dominated by the clamped representations. The present results suggest that if only ihe<br />

input image is clamped and beliefs allowed to evolve across [he whole network, these<br />

show greater contextual modulation through lateral interactions. This is illustrated in<br />

Figure 5.31 and discussed below in Section 6.1.2.5,<br />

It is also possible that the structure and parameters <strong>of</strong> the network, derived from the HMAX<br />

model and mimicking the venlral path, are not suflicient for the precise spalial refinement <strong>of</strong><br />

feedback. Indeed the dorsal path, which has been shown to be tightly interlinked with the ventral<br />

path at many levels, may play a crucial role by providing spatial and motion related information<br />

which could guide the feedback disambiguation process (Fa/,letal, 2009. Chikkeruretal, 2010.<br />

Grossberg el al. 2007). In this sense even for static images, such as those employed in this<br />

model, the continuous microsaccadic movements <strong>of</strong> the eye might be providing crucial infor­<br />

mation for perceptual completion processes (?). In this same line, George and Hawkins (2009)<br />

demonstrated that simulating saccadic movemenls in ihe input image improved the feedback<br />

reconstruction performance <strong>of</strong> the model. A more complete model <strong>of</strong> visual perception could<br />

therefore be accomplished by implementing a parallel interconnected Bayesian network thai<br />

modelled the dorsal path and provided the additional information required.<br />

Nonetheless, the results in Figure 5.28 demonstrate the ability <strong>of</strong> the model to feed back high-<br />

level information to lower levels, even in the absence <strong>of</strong> boitom-up input, consistent with evi­<br />

dence on mental imagery. Evidence has consistently shown ihat the regions and cortical repre­<br />

sentations <strong>of</strong> mental imagery are surprisingly similar to those <strong>of</strong> visual perception, suggesting<br />

boih modalities share a common substrate (Ishai 2010). Slotnick et al. (2005) showed that vi­<br />

sual mental imagery can evoke relinolopic activations in early visual regions, in agreemeni with<br />

generative modelling approaches. Recently. Reddy el al. (2010) obtained results suggesting<br />

the same pauems on neural activity generated during visual perception get reaclivaled during<br />

mental imagery, mediated by feedback connections from high-level object recognition layers.<br />

The setup where feedback originates from ;r(52) was also used to explore the different belief<br />

244

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