Previous research showed that sucrose and wheel-running reinforcement of leverpressing generate different response rate asymptotes. To investigate the basis of this difference, the present study assessed the role of inhibitory after-effects and excitatory stimulus effects on measures of responding in rats exposed to fixed-interval schedules that randomly produced either sucrose or wheel-running reinforcers. Different discriminative stimuli were associated with each reinforcer type. Inhibitory aftereffects and excitatory stimulus effects were assessed by the pattern of postreinforcement pauses and local response rates across the four different combinations of previous and upcoming reinforcer types: wheel-wheel, wheel-sucrose, sucrose-wheel, and sucrose-sucrose. Results showed that, regardless of the prior type of reinforcer, response rates were higher and pauses were shorter in the presence of a stimulus signaling sucrose reinforcement. This suggests that differences in response rate asymptotes generated by these qualitatively different reinforcers may have more to do with differences in excitatory stimulus effects than with inhibitory after-effects.In 1970, Herrnstein formulated a form ofthe matching law equation for the situation in which there is only a single source ofreinforcement arranged by the experimenter and a single measured response. In this single-operant form ofthe matching law, the response-reinforcer relation takes the form of a hyperbola that is described by the following equation:where Bl is the predicted response rate (responses/min), RI is the obtained reinforcement rate, and k and Re are estimated parameters. Specifically, k refers to the asymptotic response rate and Re is defined by the rate ofreinforcement that maintains half the asymptotic response rate. In 1998, Belke showed that response rate asymptotes in rats responding on a lever for .1 ml of 15% sucrose solution were higher than those obtained when the opportunity to run for 15 sec was the reinforcing consequence. This finding contradicts a major assumption underlying Herrnstein's (1970) single-operant form of the matching law. According to Herrnstein (1974), 'The sole determining influence on the size of [the response rate asymptote] is the response form itself, without regard to the amount or type of reinforcement conditional upon it or on anything else" (p. 163). In other words, response rate asymptotes for sucrose and wheel-running reinforcement should not differ unless the form ofa response that each reinforcer is contingent upon differs.More recently, studies using sucrose and water reinforcement produced results that violate this assumption. Dallery, McDowelI, and Lancaster (2000) showed that response rate asymptotes within the same animal were relatively constant across sucrose concentrations ranging from 0.64 to 0.2 M, but decreased at the concentrations of0.1 and 0.05 M. McDowell and DalIery (1999) showed that for rats pressing levers for water reinforcement, response rate asymptotes remained relatively constant between 2...