Using ultrafast laser excitation and time-correlated single-photon counting techniques, we have measured the collisional mixing rates between the rubidium 5(2)P fine-structure levels in the presence of (4)He gas. A nonlinear dependence of the mixing rate with (4)He density is observed. We find Rb fine-structure transfer is primarily due to binary collisions at (4)He densities of < or = 10(19) cm(-3), while at greater densities, three-body collisions become significant. We determine a three-body collisional transfer rate coefficient (5(2)P(3/2) --> 5(2)P(1/2)) of 1.25(9)x10(-32) cm(6)/s at 22 degrees C.
Inert-gas-induced collisional transfer between the first four excited states of Sr has been measured by determining excited-state densities following pulsed laser excitation of the 5
1P state. We observe 5
1P collisional transfer exclusively to the 4
3D state, with (\ensuremath{\sim}800 K) rate coefficients ranging from 0.24 to 2.0\ifmmode\times\else\texttimes\fi{}${10}^{\mathrm{\ensuremath{-}}11}$
cm3 ${\mathrm{s}}^{\mathrm{\ensuremath{-}}1}$ for the various gases. We also measure 4
1D2 transfer primarily to the 4
3D state, with rate coefficients of 0.65 to 6.8\ifmmode\times\else\texttimes\fi{}${10}^{\mathrm{\ensuremath{-}}11}$
cm3 ${\mathrm{s}}^{\mathrm{\ensuremath{-}}1}$. The 4
3D state radiative lifetime is observed to be 2.9\ifmmode\pm\else\textpm\fi{}0.2 \ensuremath{\mu}s, collisional mixing between the 4
3Dj fine-structure levels is essentially gas kinetic (k\ensuremath{\sim}5\ifmmode\times\else\texttimes\fi{}${10}^{\mathrm{\ensuremath{-}}10}$
cm3 ${\mathrm{s}}^{\mathrm{\ensuremath{-}}1}$), and k${10}^{\mathrm{\ensuremath{-}}13}$
cm3 ${\mathrm{s}}^{\mathrm{\ensuremath{-}}1}$ for 4
3D\ensuremath{\rightarrow}5
3P collisional transfer.