More than sixty years after Alan Hodgkin presented his classification of firing patterns in the axons of the crab Carcinus maenas, the underlying mechanisms of the firing patterns are still only fragmentarily understood. Two main types have been discerned in neurons and dynamical membranes models. Type 1 shows a continuous frequency-stimulation current (f-I) relationship and thus an arbitrarily low frequency at threshold current, while Type 2 shows a discontinuous f-I relationship and a minimum frequency. Type 1 obtains rhythmicity via a saddle-node bifurcation, thus requiring three stationary potentials at subthreshold stimulation current. Type 2 obtains rhythmicity via a Hopf or double-orbit bifurcation. In a previous investigation of a hippocampal neuron model we showed that the membrane density of critical ion channels could regulate the bifurcation type and consequently the threshold dynamics. In the present study we extend our previous analysis to other quantitatively well-described excitable membranes. These studies show that not merely the channel density, but the overall structure of the phase space around the stationary potentials determine the onset frequency. We show, by means of techniques from nonlinear dynamical system theory, that this phase space is altered both by changes in channel density and channel kinetics. Understanding these interactions is an important step towards understanding global oscillatory activity in brain networks.