I am having some fundamental misunderstanding I think in my simulation of a pump-probe experiment. Take, for example, a medium that has a resonant frequency at 266 nm. I am pumping it with a Gaussian beam centered at that wavelength with some defined bandwidth. Assuming, for simplicity, the sample is a collection of Lorentz oscillators, and foregoing any time-dependence on the population (just a simple zero-time signal), my model for the resonant polarization is:
$$ P_\mathrm{resonant} = \frac{Ne^2}{m_0}\frac{1}{(\omega_0^2 - \omega^2 - i\gamma\omega)} \epsilon$$
There are constants (density of atoms, etc.), but what's important here is whether or not we are at the resonant frequency. Where $\epsilon$ is my incoming electric field, of which I will define as:
$$\epsilon = \mathrm{Re}(\epsilon_0(\exp(-i(\omega t + \phi)))) = \epsilon_0\cos(\omega t + \phi) $$
Thus, my signal will be: $\epsilon_\mathrm{signal} = \epsilon_\mathrm{pump/probe} + P_\mathrm{resonant}$
What I am doing is determining what $P_\mathrm{resonant}$ is at each wavelength/frequency of my Gaussian pulse. However, I'm not sure how to deal with the electric field, as I'm interested in the resulting signal; I am thinking it is equivalent to the amplitude of the interfered field (the modulus of it), but I can't seem to figure it out; I would like to pass my probe pulse (another Gaussian) through the sample and measure its interaction (whether it is transient gain or absorption), but I am not certain how to achieve that part. Can anybody help me understand this part?