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At least 19 recordsLinked to original sources

Cultural coevolution of norm adoption and enforcement when punishers are rewarded or non-punishers are punished.

A number of studies have shown that social norms can be maintained at a high frequency when norm-violators are punished. However, there remains the problem of how norm-adopters and punishers coevolve within a single group. We develop a recursive system to examine the coevolution of norm-adopters and punishers where the viability of punishers is enhanced by one of two "metanorms": (1) Norm-observers reward punishers for punishing norm-violators (Reward Model); (2) Punishers punish non-punishers (Punishment Model). Both models generate a bistable system and each is characterized in phenotype frequency space by a distinct region of attraction to the equilibrium consisting of only norm-adopting punishers. Using a Monte Carlo simulation, we find that cultural drift may allow norm-adopters and punishers to coevolve from invasion into this region of attraction, resulting in their fixation. This coevolution typically occurs across a wider range of conditions under the reward- than the punishment-based metanorm. We also show that, under appropriate conditions, a large negative statistical association between the two traits may evolve only under the Reward Model. Furthermore, for each metanorm, a population of norm-adopters who always observe the norm can be locally stable over a continuum of punishment frequencies.

Cultural Evolution↗

The coevolution of altruism and punishment: role of the selfish punisher.

Punishment is an important mechanism promoting the evolution of altruism among non-relatives. We investigate the coevolution of altruism and punitive behavior, considering four possible strategies: the altruist punisher (AP, a cooperator who punishes defectors), the altruist non-punisher (AN, a pure cooperator), the selfish punisher (SP, a defector who punishes defectors), and the selfish non-punisher (SN, a pure defector). The SP uses a paradoxical strategy as it punishes other defectors. We analyse the effects of SP and AN on the coevolution of altruism and punishment. We study both the score-dependent viability model (whereby the game's score affects survivorship only) and the score-dependent fertility model (whereby the score affects fertility only). In the viability model of a completely mixed population, SP first drives out SN, and hence it helps cooperators (AP and AN) to evolve. In contrast, in the fertility model of a completely mixed population, neither SP nor AN helps the evolution of cooperation. In both the viability and fertility models of a lattice-structured population, SP promotes the spread of AP. In contrast, AN discourages the evolution of AP. These results can be understood that punishment is a form of spite behavior, paying a cost to reduce the fitness of the opponents, and that different models give different magnitude of advantage to spite behavior.

Altruism↗

Drugs and punished responding. II. d-Amphetamine-induced increases in punished responding.

The effects of d-amphetamine on punished responding were studied in two experiments. In Experiment I, pigeons responded under a multiple fixed-ratio 30 response fixed-interval 5-min schedule of food presentation with 60-sec limited holds in both components. Each response was punished with electric shock, the intensity of which was varied systematically. In Experiment II, another group of pigeons responded under a multiple fixed-interval 5-min fixed-interval 5-min schedule of food presentation with 40-sec limited holds. Each response was punished with shock during one component, and every thirtieth response was punished in the other component. d-Amphetamine increased overall rates of punished responding only rarely under any of the punishment conditions; however, response rates within the fixed-interval when rates were low were increased by d-amphetamine when the shock intensity was low (Experiment I), or when responses produced shock intermittently (Experiment II). The data suggest that the effects of d-amphetamine on punished responding depend on the control rate of responding, the punishment intensity, the punishment frequency, and the schedule of food presentation.

Animals↗

Punishment-specific effects of pentobarbital: dependency on the type of punisher.

Pigeons were trained to peck a key under a multiple random-interval 1-minute, random-interval 6-minute schedule of food presentation. Subsequently, over three phases, additions were made during the random-interval 1-minute component as follows: pecks during the component occasionally were punished by timeout presentation (Phase 1), timeouts were presented independently of responding during the component (Phase 2), pecks during the component occasionally were punished by electric-shock presentation (Phase 3). In Phases 1 and 3, response-dependent timeout and shock suppressed responding and established equivalent rates in both components of the multiple schedule. Intermediate doses of pentobarbital increased responding suppressed by electric-shock punishment but had little or no effect on responding suppressed by timeout punishment. Response-independent presentation of timeouts did not result in suppression of responding (thus showing that response-dependent timeout acted as a punisher), and pentobarbital did not reliably increase unpunished responding. Pentobarbital's selective "punishment-attenuating" properties depend on the nature of the punisher.

Animals↗

Effects of d-amphetamine and of diazepam on non-punished and punished schedule-induced drinking in rats.

Drinking induced in food-deprived rats by a Fixed-Time 1min schedule of food presentation was measured by the amount of water consumed per session and the number of licks per inter-food interval. Subsequently each lick initiated a 10-sec signalled delay in the delivery of food, which led to a decrease in drinking (punishment). With three rats the effects of d-amphetamine (0.25, 0.5, 1.0, 2.0mg/kg) were assessed on non-punished and then on punished drinking. With another three rats, the effects of diazepam (0.5, 1.0, 2.0, 4.0mg/kg) were assessed. The smaller doses of d-amphetamine had no consistent effect on overall measures of non-punished schedule-induced drinking, but the largest dose decreased them. With the signalled delay d-amphetamine increased punished schedule-induced drinking. Non-punished drinking was increased by small doses of diazepam and decreased by the largest dose, but no dose of diazepam affected punished drinking.

Journal Article↗

Effects of spirometric administration of tobacco smoke containing varying amounts of nicotine on human punished and non-punished operant responding.

Lever pulling of male tobacco smokers was maintained by a variable interval 20sec schedule (VI 20) of point presentation. In experiment 1 the rate of lever pulling was suppressed by a punishment contingency which stipulated that lever pulls would produce point subtractions on a variable ratio 30 schedule (VR 30). In experiment 2 the punishment contingency was omitted. Each subject participated in eight sessions each day (Mon. through Fri.). Each block of two 20-min sessions was separated by a period during which tobacco smoke containing varying amounts of nicotine was administered by the spirometry method, which ensured a constant puff volume and deep inhalation. The tobacco smoke conditions were: (1) 0.3mg nicotine yield cigarettes (baseline condition), (2) 1.2mg nicotine yield cigarettes, (3) 2.7mg nicotine yield cigarettes and (4) a condition in which room-temperature air was administered. Subjects remained at baseline conditions until responding stabilized and were then exposed to higher nicotine yield smoke or air for an entire day. Subjects were then returned to baseline conditions before administration of higher nicotine yield smoke or air. In experiment 1 (punishment contingency) lever pulling decreased as a function of increasing nicotine content in tobacco smoke. This effect upon responding was similar to the effects of CNS stimulants on punished responding in non-human subjects. In experiment 2 (no punishment contingency), no consistent effect of tobacco smoke or non-punished responding was observed.

Journal Article↗

Why do we punish? Deterrence and just deserts as motives for punishment.

One popular justification for punishment is the just deserts rationale: A person deserves punishment proportionate to the moral wrong committed. A competing justification is the deterrence rationale: Punishing an offender reduces the frequency and likelihood of future offenses. The authors examined the motivation underlying laypeople's use of punishment for prototypical wrongs. Study 1 (N = 336) revealed high sensitivity to factors uniquely associated with the just deserts perspective (e.g., offense seriousness, moral trespass) and insensitivity to factors associated with deterrence (e.g., likelihood of detection, offense frequency). Study 2 (N = 329) confirmed the proposed model through structural equation modeling (SEM). Study 3 (N = 351) revealed that despite strongly stated preferences for deterrence theory, individual sentencing decisions seemed driven exclusively by just deserts concerns.

Adult↗