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PubMed2005

Flexural strengths of denture base resin repaired with autopolymerizing resin and reinforcements after thermocycle stressing.

PURPOSE: Fracture of an acrylic denture base is a common problem in prosthodontic practice. Although various reinforcement methods have been used, when a fractured denture base is repaired with autopolymerizing resin recurrent fractures frequently occur at the repairing interface or adjacent areas. The purpose of this study was to evaluate the maximum flexural load of denture base resin repaired with autopolymerizing resin and several reinforcement systems after thermocycle stressing. MATERIALS AND METHODS: Rectangular (10 x 70 x 3 mm) flexural specimens were fabricated by repairing a pair of heat-cured denture base resin specimens using autopolymerizing resin and a series of reinforcement materials. The materials included 4 metal wires and a woven glass fiber. Each reinforcement was embedded in the center of the specimens. Flexural specimens repaired without reinforcement were prepared as controls. Specimens were subjected to 50,000 thermocycles (4 approximately 60 degrees C, 1-minute dwell time). A 3-point flexural test was carried out by loading the center of the repaired site at 5 mm/minute crosshead speed with 50 mm span jig supports. The load necessary to cause fracture was recorded for each specimen. All data were statistically analyzed using ANOVA and the Bonferroni/Dunn test (alpha < 0.05). RESULTS: The average load to fracture of specimens repaired with nonreinforced autopolymerizing resin was 68.4 N after 50,000 thermocycles. Specimens reinforced with 1.2 mm diameter stainless steel wire exhibited the highest value (89.8 N). The value for specimens reinforced with 1.2 mm diameter Co-Cr-Ni wire was 86.6 N. These fracture loads were significantly higher than those for specimens without reinforcement (p < 0.05). Low elasticity reinforcement, such as pure titanium wires, woven metal wire, and woven glass fiber were not effective in increasing the load to fracture values of flexural specimens. CONCLUSIONS: Specimens reinforced with 1.2 mm diameter stainless steel wires or Co-Cr-Ni wires resulted in significantly higher loads to fracture as compared to specimens without reinforcement. The use of pure titanium wire, woven metal wire, and woven glass fiber did not improve the fracture loads.

Acrylic Resins↗
PubMed1976

The effects of unsignalled delayed reinforcement.

Pigeons' pecks were reinforced according to a variable-interval schedule. A delay-of-reinforcement procedure was then added to the schedule, or a yoked-control procedure was arranged where the reinforcers occurred independently of responding according to the same variable-interval schedule. During the delay-of-reinforcement procedure, the first peck after a reinforcer was scheduled began a delay timer and the reinforcer was delivered at the end of the interval. No stimulus change signalled the delay interval and responses could occur during it, so that the obtained delays were often shorter than those scheduled. Responding under this procedure was highly variable but, in general, behavior was substantially reduced even with the shortest delay used, 3 sec. In addition, the rates maintained by delayed reinforcement were only slightly greater than those maintained by the yoked-control procedure, suggesting that adventitious pairings of response and reinforcer were responsible for some of the maintenance of behavior that did occur. The results challenge recent conceptions of reinforcement as involving response-reinforcer correlations and re-emphasize the role of temporal proximity between response and reinforcer.

Journal Article↗
PubMed1976

Effects of concurrent response-independent reinforcement on fixed-interval schedule performance.

In three experiments, behavior maintained by fixed-interval schedules changed when response-independent reinforcement was delivered concurrently according to fixed- or variable-time schedules. In Experiment I, a pattern of positively accelerated responding during fixed interval was changed to a linear pattern when response-independent reinforcement occurred under a variable-time schedule. Overall response rates (total responses/total time) decreased as the frequency of response-independent reinforcement increased. Experiment II showed that the response-rate changes in the first experiment were controlled by the response-reinforcer relation, but the changes in patterns of responding were similar whether concurrently available reinforcement at varying times was response-dependent or response-independent. In the final experiment, the addition of response-independent reinforcement at fixed times to a fixed-interval schedule resulted in changes in both local and overall response rates and in the occurrence of positively accelerated responding between reinforcements. These results suggest that the temporal distribution of reinforcers determines response patterns and that both the response-reinforcement dependency and the schedule of reinforcement determine overall response rates during concurrently scheduled response-dependent and response-independent reinforcement.

Journal Article↗
PubMed1978

Time allocation in concurrent schedules: the effect of signalled reinforcement.

The responses of five pigeons were reinforced on concurrent variable-interval variable-interval reinforcement schedules in which changeover key responses changed the stimulus and reinforcement schedules associated with the food key. While the reinforcement availability in one component remained unchanged throughout the experiment, the reinforcement availability in the other component was, during several conditions, signalled by the onset of an additional discriminative stimulus. During unsignalled conditions, both the relative frequency of responding and the relative time spent in each component approximated the obtained relative reinforcement frequency in each component. The effect of signalling reinforcer availability in one component was to (1) reduce responding in the signalled component to near-zero levels, and (2) increase the relative time in the unsignalled component, without a corresponding increase in the obtained relative reinforcement frequency. The magnitude of the increase in relative time in the unsignalled component decreased as the overall frequency of reinforcement increased. This deviation in the matching relation between relative time and the obtained relative reinforcement frequency was eliminated if the overall reinforcement frequency was increased before the signal was introduced and then, without removing the signal, gradually reduced.

Journal Article↗
PubMed1979

Decision rules and signal detectability in a reinforcement-density discrimination.

Two probabilistic schedules of reinforcement, one richer in reinforcement, the other leaner, were overlapping stimuli to be discriminated in a choice situation. One of two schedules was in effect for 12 seconds. Then, during a 6-second choice period, the first left-key peck was reinforced if the richer schedule had been in effect, and the first right-key peck was reinforced if the leaner schedule had been in effect. The two schedule stimuli may be viewed as two binomial distributions of the number of reinforcement opportunities. Each schedule yielded different frequencies of 16 substimuli. Each substimulus had a particular type of outcome pattern for the 12 seconds during which a schedule was in effect, and consisted of four consecutive light-cued 3-second T-cycles, each having 0 or 1 reinforced center-key pecks. Substimuli therefore contained 0 to 4 reinforcers. On any 3-second cycle, the first center-key peck darkened that key and was reinforced with probability .75 or .25 in the richer or leaner schedules, respectively. In terms of the theory of signal detection, detectability neared the maximum possible d' for all four pigeons. Left-key peck probability increased when number of reinforcers in a substimulus increased, when these occurred closer to choice, or when pellets were larger for correct left-key pecks than for correct right-key pecks. Averaged over different temporal patterns of reinforcement in a substimulus, substimuli with the same number of reinforcers produced choice probabilities that matched relative expected payoff rather than maximized one alternative.

Journal Article↗
PubMed1988

Concurrent-schedule performance: Effects of relative and overall reinforcer rate.

Six pigeons were trained to respond on two keys, each of which provided reinforcers on an arithmetic variable-interval schedule. These concurrent schedules ran nonindependently with a 2-s changeover delay. Six sets of conditions were conducted. Within each set of conditions the ratio of reinforcers available on the two alternatives was varied, but the arranged overall reinforcer rate remained constant. Each set of conditions used a different overall reinforcer rate, ranging from 0.22 reinforcers per minute to 10 reinforcers per minute. The generalized matching law fit the data from each set of conditions, but sensitivity to reinforcer frequency (a) decreased as the overall reinforcer rate decreased for both time allocation and response allocation based analyses of the data. Overall response rates did not vary with changes in relative reinforcer rate, but decreased with decreases in overall reinforcer rate. Changeover rates varied as a function of both relative and overall reinforcer rates. However, as explanations based on changeover rate seem unable to deal with the changes in generalized matching sensitivity, discrimination accounts of choice may offer a more promising interpretation.

Journal Article↗
PubMed1989

Children's choice: Sensitivity to changes in reinforcer density.

Two experiments were carried out in which children's sensitivity to changes in reinforcer density (number of reinforcers per session) was measured in a choice paradigm. In Experiment 1, 24 girls (ages 6, 9, and 12 years) performed on concurrent-chain schedules of reinforcement. The initial links were variable-interval 10-s schedules. One terminal link always gave three tokens after 30 s, but the parameters associated with the other were varied. Independent manipulations of reinforcer size (two tokens or four tokens) and prereinforcement delay (25 s or 65 s) led to equal changes in the relative density of tokens that could be earned on the schedules. Subjects at all ages were sensitive to changes in reinforcer density brought about by changes in reinforcer size, whereas only 3 12-year-olds showed sensitivity to the changes brought about by manipulation of prereinforcer delay. In Experiment 2, titration procedures were used to test the extent of this insensitivity to delay in 32 6- and 12-year-old children. In these procedures, a repeated choice of the large reinforcer increased the delay to its delivery, and a repeated choice of the small reinforcer reduced the delay to the delivery of the large reinforcer. Whereas 6-year-old boys and girls tended to maintain a strong preference for the large reinforcer, so increasing the delay to its delivery, 12-year-olds tended to distribute their responses to both alternatives, thus producing a stable level of delay to the large reinforcer. The results from the two experiments support the idea of two stages in the development of adaptive intertemporal choice.

Journal Article↗
PubMed1989

Sensitivity of time allocation to an overall reinforcer rate feedback function in concurrent interval schedules.

Six pigeons were trained on concurrent variable-interval schedules in which feedback functions arranged that the overall reinforcer rate either (a) was independent of preference, (b) decreased with increasing absolute preference, or (c) increased with increasing absolute preference. In Experiment 1, the reinforcer rate in an interreinforcement interval was determined by the absolute time-allocation ratio in the previous interval. When arranged reinforcer ratios were varied, there was no evidence of control over preference by overall reinforcer rate. In Experiment 2, the feedback function arranged that reinforcer rates were an inverse function of absolute preference, and window durations were fixed times. In Phase 1, using schedules that provided a four-to-one reinforcer ratio, the window duration was decreased from 20 s to 5 s over four conditions. Then, in Phases 2 and 3, the arranged reinforcer ratios were varied. In Phase 2, the reinforcer rate in the current 5-s time window was determined by preference in the previous 5-s window, and in Phase 3, the window durations were 20 s. Again, there was no indication of control by obtained overall reinforcer rate. These data call into question theories that suggest that the process underlying matching is one of maximizing overall reinforcer rates, or that preference in concurrent aperiodic schedules is controlled to any extent by overall reinforcer rate. They also question the notion that concurrent-schedule preference is controlled by molecular maximizing.

Journal Article↗
PubMed1994

Reinforcer magnitude (sucrose concentration) and the matching law theory of response strength.

This experiment investigated the relationship between reinforcer magnitude (sucrose concentration) and response rate. The purpose was to evaluate the behavior of two parameters of an equation that predicts absolute response rate as a function of reinforcement rate and two free parameters. According to Herrnstein's (1970) theory of reinforced behavior, one parameter of this "response-strength equation" measures the efficacy of the reinforcer maintaining responding and the other parameter measures motoric components of response rate, such as response duration. Seven rats served as subjects. Experimental sessions consisted of a series of five different variable-interval schedules of reinforcement, each in effect for 5 minutes. Within each session, obtained reinforcement rates varied over more than a 30-fold range, from about 20 per hour to 700 per hour. The reinforcer was sucrose solution, and, between sessions, its concentration was varied from 0.0 to 0.64 molar (0 to 21.9%). For sucrose concentrations of 0.16 to 0.64 m, response rate was a negatively accelerated function of reinforcement rate. Increases in sucrose concentration increased response rates maintained by low but not high reinforcement rates. This pattern of changes corresponds to a change in the reinforcement-efficacy parameter of the response-strength equation. In contrast, the motor-performance parameter did not change as a function of sucrose concentration. These findings are inconsistent with the results of a similar study (Bradshaw, Szabadi, & Bevan, 1978) but support Herrnstein's theory of reinforced behavior.

Journal Article↗
PubMedDate not supplied

Influence of veneering composite composition on the efficacy of fiber-reinforced restorations (FRR).

This study investigated the influence of fiber reinforcement on the flexural properties of four commercial (Artglass, Belleglass HP, Herculite XRV and Solidex) veneering composites (Series A) and two experimental composites (Series B&C). This study investigated how the composition of the veneering composites influenced the enhancement of strength and modulus produced by fiber reinforcement. The formulation of the experimental composites were varied by changing the filler load (Series B) or the resin matrix chemistry (Series C) to assess the effect these changes would have on the degree of reinforcement. In Series A, the commercial veneering composites were reinforced by an Ultra-High-Molecular-Weight Polyethylene fiber (UHMW-PE/Connect) to evaluate flexural properties after 24 hours and six months. In Series B, experimental composites with the same organic matrix but with different filler loads (40% to 80% by weight) were also reinforced by Connect fiber to evaluate flexural properties. In Series C, experimental composites (Systems 1-4) with the same filler load (76.5% by weight) but with different organic matrix compositions were reinforced by Connect fiber to evaluate flexural properties. For Series B and C, flexural properties were evaluated after 24 hours water storage. All the samples were prepared in a mold 2 mm x 2 mm x 25 mm and stored in distilled water at 37 degrees C until they were ready for flexural testing in an Instron Universal Testing Machine using a crosshead speed of 1 mm/minute. The results showed no significant differences in the flexural strength (FS) between any of the commercial reinforced composites in Series A. The flexural modulus (FM) of the fiber-reinforced Belleglass HP group was significantly higher than for Artglass and Solidex. Water storage for six months had no significant (p>0.05) effect on the flexural strength of three of the four reinforced veneering composites. The flexural strength for Artglass was significantly reduced (p<0.05) by six-month water storage. In Series B, however, increasing the amount of filler loading improved the flexural modulus of the reinforced experimental composite but had no effect on its flexural strength. In Series C, changing the organic matrix formulation had no affect on flexural strength but affected the flexural modulus of the reinforced experimental composite.

Analysis of Variance↗
PubMed1992

Effects of methylphenidate on response rate and measures of motor performance and reinforcement efficacy.

This experiment evaluated the effects of methylphenidate on reinforced responding in rats. In each session the subjects (rats) earned reinforcement on seven different variable-interval reinforcement schedules. The average intervals varied from 108 to 3 s and provided reinforcement rates ranging from about 30 to 1100/h. Response rate was a negatively accelerated function of reinforcement rate. Low doses of methylphenidate (1.0 and 2.0 mg/kg) increased responding maintained by the four leanest schedules, but had little effect on responding maintained by the three densest schedules. In contrast, an 8.0 mg/kg dose increased responding maintained by the three densest schedules and slightly decreased responding maintained by leaner schedules. A quantitative model of reinforced responding, referred to as the matching law or response strength equation, was fitted to the data. This equation has two parameters. On the basis of previous experiments, one was used to measure changes in reinforcement efficacy and the other was used to measure changes in motor performance. The 1.0 and 2.0 mg/kg doses changed the reinforcement parameter in the same way as did increases in deprivation and reward magnitude. The 8.0 mg/kg dose changed the motor parameter in the same was as did decreases in lever weight. It was concluded that methylphenidate increases reinforcement efficacy, and that the highest dose changed the topography of responding. The results are discussed in terms of the response strength equation, the rate dependency principle, and the question of how to interpret changes in reinforcement efficacy and motor performance.

Animals↗
PubMed2004

Second-order stimuli do not always increase overall response rates in second-order schedules of reinforcement in the rat.

RATIONALE: Second-order schedules of reinforcement have been used extensively to model reward-seeking and drug-seeking behaviour. Second-order stimuli within second-order schedules have been shown to enhance response rates during operant responding for natural reinforcers and drug reinforcers. This has led some to view second-order schedules of drug reinforcement as a model maintained of drug-seeking in addicts by drug-associated stimuli. However, the functional role of the second-order stimulus within second-order schedules is complex. OBJECTIVE: We investigated the role of second-order stimuli within a second-order schedule of reinforcement [FI 4 min (FR10: S)] maintained by sweetened water reinforcement. METHODS: Eight rats were trained to press a bar on a second-order schedule of reinforcement and tested in the presence and absence of the second-order stimulus. RESULTS: In contrast to most previous work, overall bar-pressing rates were significantly increased when the second-order stimulus was omitted (second-order stimulus omission: 0.17 Hz (+/-0.04, 95% CI); second-order stimulus present: 0.13 Hz (+/-0.04, 95% CI)). However, second-order stimuli also changed the pattern of responding whereby rats would make a bout of bar presses prior to the presentation of the second-order stimulus and then pause briefly after the second-order stimulus. In the absence of second-order stimuli, responding was uniformly high. Control measures, such as the ability of the second-order stimulus to evoke checking for the primary reinforcers, indicated that the second-order stimulus was associated with the primary reinforcer. CONCLUSIONS: These results demonstrated that although second-order stimuli maintained responding and caused the rat to check for primary reinforcement, overall response rates were increased when the second-order stimuli were omitted. This has implications for interpreting the results of studies where overall response rates within second-order schedules have been the only measure used to assess the effects of potential anti-addiction drugs. Future studies could be improved by performing a second-order stimulus omission test analysing both the overall response rates and the temporal organization of responding with respect to the second-order stimulus.

Analysis of Variance↗
PubMed2005

Cocaine self-administration under fixed and progressive ratio schedules of reinforcement: comparison of C57BL/6J, 129X1/SvJ, and 129S6/SvEvTac inbred mice.

RATIONALE: Combining strains to generate mutant mice may obscure conclusions regarding the targeted gene. Specifically, cocaine may have reduced reinforcing effects in 129 substrains compared to the C57BL/6 strain, commonly used for ES cells and breeding, respectively. OBJECTIVES: We tested the hypothesis that reinforcing effects of cocaine differ between the C57BL/6J strain and two substrains of 129, 129X1/SvJ and 129S6/SvEvTac. METHODS: To assess and reduce performance differences, operant responding was established with liquid food as a reinforcer and evaluated under fixed and progressive ratio schedules. Dose-effect functions for intravenous cocaine self-administration were then determined under both schedules. Finally, reinforced and nonreinforced manipulanda were reversed to assess acquisition of self-administration using a previously nonreinforced response. RESULTS: Relative to C57BL/6J mice, 129X1/SvJ mice showed decreased reinforcing effects of low-magnitude food and cocaine reinforcers. Dose-effect functions for cocaine self-administration were comparable between C57BL/6J and 129S6/SvEvTac mice, despite delayed acquisition of operant behaviors and rightward shifts in the food concentration-effect functions in 129S6/SvEvTac mice. A high cocaine dose clearly served as a positive reinforcer in all three strains in a reversal procedure. CONCLUSIONS: Relative to C57BL/6J mice, the reinforcing effects of cocaine were diminished in 129X1/SvJ mice, but only for low cocaine doses, and a similar profile was observed with food reinforcement. 129S6/SvEvTac mice required more extensive operant training than C57BL/6J mice did, but after acquisition, reinforcing effects of cocaine were similar in the two strains. We suggest that comparable phenotypes observed in gene-targeting studies may result from genetic background, whereas more profound or qualitatively different phenotypes may be more confidently attributed to targeted mutations.

Animals↗
PubMed1975

Auditory localization of infants as a function of reinforcement conditions.

The influence of four reinforcement conditions on the auditory localization behavior of normal infants was studied. Forty-eight infants 12 to 18 months of age were assigned to one of four groups of 12 subjects each. All received 30 presentations of complex noise at suprathreshold level. After each response to the stimulus, Group 1 received no reinforcement, Group 2 received social reinforcement, Group 3 received "simple" visual reinforcement (a blinking light), and Group 4 received "complex" visual reinforcement (an animated toy animal). The two visual reinforcement conditions produced the most localization responses, followed in order by the social reinforcement and no reinforcement conditions. These results indicate that auditory localization behavior of infants is influenced by reinforcement and that the extent of this effect is related to the type of reinforcement employed.

Acoustic Stimulation↗
PubMed1996

Dopamine receptors in the medial prefrontal cortex influence ethanol and sucrose-reinforced responding.

This study tested the role of dopamine receptors in the medial prefrontal cortex (mPFC) in the onset, maintenance, and termination of ethanol and sucrose-reinforced responding. Two groups of Long Evans rats were trained to lever press on a fixed-ratio 4 schedule of reinforcement with 10% ethanol (n = 10) or 5% sucrose (n = 5) presented as the reinforcer. After implantation of injector guide cannulae, the D2/3 agonist quinpirole and the D2 antagonist raclopride were administered bilaterally into the mPFC before behavioral sessions. During control conditions, sucrose reinforcement maintained a 2-fold greater number of responses per session than did ethanol reinforcement. Quinpirole (10.0 micrograms/microliter) reduced total ethanol-reinforced responses by delaying response onset and decreasing the duration of responding, but had no effect on response maintenance (i.e., response rate). A higher dose of quinpirole (20.0 micrograms/microliter) decreased total sucrose responses by simultaneously decreasing duration and response rate, without altering response latency. Thus, the effects of quinpirole on ethanol and sucrose-reinforced responding were similar on response total and duration, but differential on response latency and rate. Raclopride (0.05 and 1.0 microgram/microliter) decreased total ethanol responding and rate, but doses as much as 400-fold greater (20.0 micrograms/microliter) did not alter sucrose response totals. Raclopride alone had no effect on response latency or duration measures in either reinforcement condition. Coadministration of raclopride blocked the quinpirole-induced increase in response latency (ethanol reinforcement) and decrease in response rate (sucrose reinforcement), but had no effect on other response measures. These data are consistent with the interpretation that D2 and D3 receptors in the mPFC are differentially involved in ethanol and sucrose response onset and maintenance, but similarly involved in response termination. However, differences in baseline response parameters and group size may have contributed to the observed effects.

Animals↗
PubMed1963

Reinforcement of mediating behavior on a spaced-responding schedule.

This paper describes a procedure for gaining experimental control over mediating behavior on a spaced-responding schedule of food reinforcement. Three rats, food-deprived, were trained on a DRL 16 sec schedule of food reinforcement. Then, a concurrent schedule of food reinforcement was introduced on a second (mediating) lever, such that the first response to occur on the mediating lever, after the DRL interval had timed out, was reinforced with food, as was the next response to occur on the DRL lever. Reinforcement via the mediating lever became a discriminative stimulus for a food-reinforcement opportunity on the DRL lever. Next, food reinforcement for the mediating behavior was replaced by a conditioned reinforcer consisting of onset of a buzzer signaling timing-out of the DRL interval. Under these conditions, chaining of behavior on the two levers was strong, and timing on the DRL lever was more accurate than under ordinary DRL conditions. As the DRL requirement was lengthened from 16 sec to 24 sec to 60 sec, mediating behavior weakened slightly. When the inter-response requirement for food reinforcement on the DRL lever was made shorter than the inter-response requirement for conditioned reinforcement on the mediating lever, the mediating behavior extinguished. Performance in the experiment was analyzed into a four-component chain, and the factors contributing to the maintenance, and later extinction, of mediating behavior are discussed.

Animals↗
PubMed1991

[Response occurrence to the non-reinforced alternative through punishment in rats].

Each of eight rats was located in the experimental chamber mounted with two levers. Lever-pressing to either of the two was maintained by a schedule of food. After that, a punishment schedule of electric shocks was added. Neither the reinforcement nor the punishment schedule was programmed on the other lever, i.e. the non-reinforced alternative. The effect of reinforcement, and the joint effect of reinforcement and punishment on responses to the non-reinforced alternative were compared. During punishment sessions, responses to the non-reinforced alternative occurred significantly more often than during reinforcement sessions. The number of responses to the non-reinforced alternative was negatively correlated with that to the reinforced alternative during punishment sessions. Nevertheless, the occurrence of responses to the non-reinforced alternative was mainly observed during the first few sessions in punishment schedule, or after stepping up the intensity of electric shock. These results were discussed in relation to the two theories and models of punishment. The results imply that the two theories and models of punishment are necessary to explain the effect of punishment.

Animals↗
PubMed1994

Prolonged behavioral effects of in utero exposure to lead or methyl mercury: reduced sensitivity to changes in reinforcement contingencies during behavioral transitions and in steady state.

Postnatal exposure to lead or methyl mercury results in mental retardation, learning deficits, and other neurobehavioral effects in humans, and adverse consequences of prenatal exposure have been clearly documented with methyl mercury. To examine the developmental neurotoxicity of these metals, especially lead, concurrent schedules of food reinforcement were used to identify learning deficits in squirrel monkeys exposed during gestation to either methyl mercury or lead. Pregnant squirrel monkeys were administered methyl mercury (0.7 to 0.9 ppm in maternal blood) or lead (21 to 79 micrograms/dl in maternal blood) during the last half to two-thirds of gestation. At about 5-6 years of age, offspring were trained to lever press under concurrent schedules of reinforcement in which separate random interval reinforcement schedules operated independently on two levers. Reinforcement densities were varied such that 20 to 90% of the reinforcers were programmed to derive from the left lever (i.e., one lever was "richer" than the other). At steady state, the behavior of the controls was sensitive to reinforcement density and showed little lever bias, but the behavior of monkeys exposed to more than 40 micrograms/dl of lead and to methyl mercury was less sensitive to reinforcement rates and heavily biased. When relative reinforcement density on a lever changed, the unexposed animals' response rates gradually shifted to the newly rich lever. The behavior of monkeys exposed to methyl mercury or more than 40 micrograms/dl of lead changed slowly, not at all, or in the wrong direction. Steady-state behavior of monkeys exposed to less than 40 micrograms/dl resembled controls, but acquisition progressed more slowly and required 2-4 times as many reinforcers to complete. These effects suggest a behavioral mechanism--insensitivity to changing reinforcement contingencies--by which learning deficits and behavioral changes associated with these metals might be related to toxicant exposure. Since maternal blood levels corresponded to those that could be experienced in occupational settings, the present data raise the possibility of fetal hazards associated with maternal lead exposures at levels tolerated in humans in occupational settings.

Animals↗