In recent neurophysiological experiments stimulus-related neuronal osc
illations were discovered in various species. The oscillations are not
persistent during the whole time of stimulation, but instead seem to
be restricted to rather short periods, interrupted by stochastic perio
ds. In this contribution we argue, that these observations can be expl
ained by a bistability in the ensemble dynamics of coupled integrate a
nd fire neurons. This dynamics can be cast in terms of a high-dimensio
nal map for the time evolution of a phase density which represents the
ensemble state. A numerical analysis of this map reveals the coexiste
nce of two stationary states in a broad parameter regime when the syna
ptic transmission is nonlinear. The one state corresponds to a stochas
tic firing of individual neurons, the other state describes a periodic
activation. We demonstrate that under the influence of additional ext
ernal noise the system can switch between these states, in this way re
producing the experimentally observed activity. We also investigate th
e connection between the nonlinearity of the synaptic transmission fun
ction and the bistability of the dynamics. To this purpose we heuristi
cally reduce the high-dimensional assembly dynamics to a one-dimension
al map, which in turn yields a simple explanation for the relation bet
ween nonlinearity and bistability in our system.