The sense of smell originates in a diverse array of receptor neurons, compr
ising up to 1000 different types. To understand how these parallel channels
encode chemical stimuli, we recorded the responses of glomeruli in the olf
actory bulbs of the anesthetized rat, by optical imaging of intrinsic signa
ls. Odor stimulation produced two kinds of optical responses at the surface
of the bulb: a broad diffuse component superposed by discrete small spots.
Histology showed that the spots correspond to individual glomeruli, and th
at similar to 400 of them can be monitored in this way. Based on its wavele
ngth-dependence, this optical signal appears to derive from changes in ligh
t scattering during neural activity. Pure odorants generally activated seve
ral glomeruli in a bilaterally symmetric pattern, whose extent varied great
ly with concentration. A simple formalism for ligand binding accounts quant
itatively for this concentration dependence and yields the effective affini
ty with which a glomerulus responds to an odorant. When tested with aliphat
ic molecules of increasing carbon chain length, many glomeruli were sharply
tuned for one or two adjacent chain lengths. Glomeruli with similar tuning
properties were located near each other, producing a systematic map of mol
ecular chain length on the surface of the olfactory bulb. Given local inhib
itory circuits within the olfactory bulb, this can account for the observed
functional inhibition between related odors. We explore several parallels
to the function and architecture of the visual system that help interpret t
he neural representation of odors.