A Mirror-Symmetric Excitatory Link Coordinates Odor Maps across Olfactory Bulbs and Enables Odor Perceptual Unity.

Sensory input reaching the brain from bilateral and offset channels is nonetheless perceived as unified. This unity could be explained by simultaneous projections to both hemispheres, or inter-hemispheric information transfer between sensory cortical maps. Odor input, however, is not topographically organized, nor does it project bilaterally, making olfactory perceptual unity enigmatic. Here we report a circuit that interconnects mirror-symmetric isofunctional mitral/tufted cells between the mouse olfactory bulbs. Connected neurons respond to similar odors from ipsi- and contra-nostrils, whereas unconnected neurons do not respond to odors from the contralateral nostril. This connectivity is likely mediated through a one-to-one mapping from mitral/tufted neurons to the ipsilateral anterior olfactory nucleus pars externa, which activates the mirror-symmetric isofunctional mitral/tufted neurons glutamatergically. This circuit enables sharing of odor information across hemispheres in the absence of a cortical topographical organization, suggesting that olfactory glomerular maps are the equivalent of cortical sensory maps found in other senses.

Klein tunneling in deformed honeycomb lattices.

We study the scattering of waves off a potential step in deformed honeycomb lattices. For deformations below a critical value, perfect Klein tunneling is obtained; i.e., a potential step transmits waves at normal incidence with nonresonant unit-transmission probability. Beyond the critical deformation a gap forms in the spectrum, and a potential step perpendicular to the deformation direction reflects all normally incident waves, exhibiting a dramatic transition form unit transmission to total reflection. These phenomena are generic to honeycomb lattices and apply to electromagnetic waves in photonic lattices, quasiparticles in graphene, and cold atoms in optical lattices.