Problems of inconsistent initial pH in peat moss-based substrates that are created using standard formulas for limestone additions, and pH drift from the target in those substrates may be due to variations in the CEC and BS of peat moss. This study was conducted to determine whether such variation exists. Sixty-four peat moss samples were obtained from several bogs across Alberta, Canada. Adsorbed cations on each peat moss sample were displaced with hydrochloric acid (HCl), and flushed out with three deionized water washes. The displacing/flushing solution was collected and later analyzed for concentration of bases (Ca, Mg, K, and Na) using atomic absorption spectrometry. After cations were removed, the peat moss exchange sites were saturated with barium acetate [Ba(OAc)2] to displace the H+, which were then collected by a second flushing with deionized water. This second displacing/flushing solution was titrated with measured amounts of NaOH to a phenolphthalein end point. Base saturation and CEC were calculated. There were significant variations in CEC (ranging from 108.12 to 162.25 cmol·kg-1) and BS (ranging from 13.52% to 63.97% of CEC) among the peat moss samples. Ca accounted for 78.08% of the BS. For a given peat moss, the higher the BS, the lower the neutralization requirement to achieve a target pH. Also, high CEC peat mosses may have greater buffering capacity than those with low CEC, which may result in less pH drift.