The responses of projection neurons in the antennal robe of the locust
brain (the functional analog of mitral-tufted cells in the vertebrate
olfactory bulb) lo natural blends and simple odors were studied with
multiple intra- and extracellular recordings in vivo. Individual odors
evoked complex temporal response patterns in many neurons. These patt
erns differed across odors for a given neuron and across neurons for a
given odor, but were stable for each neuron over repealed presentatio
ns (separated by seconds to minutes) of the same odor. The response of
individual neurons to an odor was superimposed on an odors specific c
oherent oscillatory population activity. Each neuron usually participa
ted in the coherent oscillations during one or more specific epochs of
the ensemble activity. These epochs of phase locking were reliable fo
r each neuron over tens of repeated presentations of one odor. The tim
ing of these epochs of synchronization differed across neurons and odo
rs. Correlated activity of specific pairs of neurons, hence, generally
occurred transiently during the population response, at times that we
re specific to these pairs and to the odor smelled. The field potentia
l oscillations, therefore, fail to reveal a progressive transformation
of the synchronized ensemble as the response to the odor unfolds. We
propose that (1) odors are represented by spatially and temporally dis
tributed ensembles of coherently firing neurons, and (2) the field pot
ential oscillations that characterize odor responses in the olfactory
system occur, at least in this animal, in parallel with a slower dynam
ic odor representation.