Hemispheric specialization is a widespread feature of vertebrate nervous systems, but the minimal conditions under which bilateral systems differentiate, acquire polarity, and retain asymmetric states remain unclear. Here, we examined these issues using a minimal evolutionary model with two initially equivalent processing channels. Each channel evolved a spatial integration width while receiving the same input, and fitness rewarded the magnitude of a bilateral mismatch-separation signal rather than explicit anomaly localization. Under exact developmental symmetry, 40 lineages evolved robust left–right differences in integration width without significant directional fixation (median |Δa| = 2.511; 22 right-wider, 18 left-wider). Weak developmental gain asymmetry biased polarity selection in a graded manner, shifting outcomes toward right-wider or left-wider solutions depending on bias direction. Forced-symmetry, shared-parameter, and single-channel controls showed that high performance depended on allowing differentiated bilateral processing. After biased solutions were reseeded under restored symmetry, differentiation was retained and amplified (median |Δa| > 6.6), consistent with history-dependent persistence within the sampled fitness landscape. Structured backgrounds increased differentiation magnitude but imposed greater decision-time costs. These results distinguish differentiation, polarity bias, and persistence as separable components of minimal hemispheric specialization.
Yamaki et al. (Sat,) studied this question.