Gender and aggression I: Perceptions of aggression

To investigate how gender and ethnicity influence evaluation, perceptions, and stereotyping of aggression, two studies were conducted with 115 college students (56% male; 50% Anglo and 26% Hispanic) and 79 individuals (72% male; 92% Anglo) who worked on a military base. Participants were asked to respond to four scenarios depicting aggressive interactions in which the gender of the protagonists varied, give their perceptions of 25 potentially aggressive incidents, and answer questions concerning stereotypes of gender related to these incidents and personal aggressive behaviors. Consistent with previous research on gender and aggression, both studies found that the aggressor, target, and respondent all affected perceptions of aggression and likelihood of aggressive behaviors. Aggression from a male and aggression directed towards a female were particularly likely to be evaluated negatively. Age and educational level were both negatively related to tolerance for aggression, and Anglo vs. Hispanic ethnicity was also associated with perceptions of aggression.We would like to thank Angela Bennett, Gail Bliss, Kayleigh Carabajal, Julie Depree, Carmen Gonzales, Deborah Good, Scott Griffin, Gladys Herrera, George Selix, Ruth Tangman, and Jon Woodland for their assistance with the development, distribution, and coding of the questionnaire.     

Extinction-induced aggression

Pigeons were conditioned to peck a response key under a procedure that alternated periods of food reinforcement with periods of extinction. The pigeons attacked a nearby pigeon at the onset of extinction. Some also attacked a stuffed model of a pigeon. The duration of attack was an inverse function of the time since the last food reinforcement and a direct function of the number of reinforcements. The pigeons attacked after the last food delivery whether or not the conditioned pecking response was required and whether or not the extinction period was signaled. The food had to be eaten; the mere sight and sound of food being delivered did not produce attack. Prior satiation reduced attack. The phenomenon was not attributable to a past history of competition between pigeons since socially deprived pigeons also attacked. Superstitious reinforcement of attack was not found to be a factor. The results indicated that the transition from food reinforcement to extinction was an aversive event that produced aggression.     

An aggression machine v. determinants in reactive aggression revisited

The relations between reactive aggression, situational cues, and emotion regulation were examined by means of the Pulkkinen Aggression Machine (PAM) task. In the PAM, provocation and response were systematically varied under two conditions: the impulsive aggression condition and the controlled aggression condition. In the impulsive condition, no information about the attacker was provided, while in the controlled condition the attackers were specified in terms of sex, age, and physical strength. The task was administered to 109 children aged 8 to 13 years. Boys (n = 61) and girls (n = 48), as well as subgroups of Adjusted (n = 67) and Maladjusted (n = 26) children were compared. The results confirmed earlier findings showing that there is a strong relationship between attack and response intensity. However, this relationship was consistently modified by the effects of situation and personality‐related variables. This meant that, while for the impulsive condition response intensity was closely tied to stimulus intensity, in the controlled condition this effect was modulated by the characteristics of the opponent: the more equal the opponent the stronger the retaliations displayed. The Maladjusted children reacted more intensively in the impulsive condition and to minor provocation in the controlled condition than the Adjusted children. This suggests that the intensity of the elicited aggression in the Maladjusted group was particularly dependent on contextual rather than internal control. Aggr. Behav. 27:430–445, 2001. © 2001 Wiley‐Liss, Inc.     

Controlling reactive aggression through cognitive evaluation of proactive aggression cues

The authors investigated how the relationship between the acts of proactive and reactive aggression was moderated by the individual differences in cognitive regulation of emotion. An aggression paradigm, a electrocardiogram recording, a cognitive assessment battery, and a short form IQ test were completed by 109 children, aged 8 to 13 years (Juujärvi, Kaartinen, Laitinen, Vanninen, & Pulkkinen, 2006 Juujärvi, P., Kaartinen, J., Laitinen, T., Vanninen, E. and Pulkkinen, L. 2006. Effects of physical provocations on heart rate reactivity, and reactive aggression in children. Aggressive Behavior, 32: 99–109. [Crossref], [Web of Science ®] , [Google Scholar]; Juujärvi, Kooistra, Kaartinen, & Pulkkinen, 2001 Juujärvi, P., Kooistra, L., Kaartinen, J. and Pulkkinen, L. 2001. An aggression machine: V. Determinants of reactive aggression revisited. Aggressive Behavior, 27: 430–445. [Crossref], [Web of Science ®] , [Google Scholar]; Lehto, Juujärvi, Kooistra, & Pulkkinen, 2003 Lehto, J. E., Juujärvi, P., Kooistra, L. and Pulkkinen, L. 2003. Dimensions of executive functioning: Evidence from children. British Journal of Developmental Psychology, 21: 59–80. [Crossref], [Web of Science ®] , [Google Scholar]). The less the children subdued the intensity of their defence to the attacks in the aggression paradigm, the poorer they performed in the cognitive assessment battery tasks measuring Working memory capacity and in the task assessing crystallised intelligence. The mean cardiovascular reactivity during the aggression paradigm was neither associated with the performances in either the cognitive assessment battery nor the intelligence tasks. Both information processing and knowledge dimensions of cognition contributed to regulation of emotion, but the respective effects of the processes cannot be inferred from the mean cardiovascular reactivity.     

Fixed-ratio schedule-induced aggression

Pigeons' pecks were conditioned with food reinforcement. Subjects were exposed to sessions of no-reinforcement and of fixed-ratio reinforcement. The pigeons attacked a target animal during the fixed-ratio reinforcement conditions. The attack occurred primarily during the post-reinforcement pause and occurred after almost every instance of reinforcement. Little or no aggressive behavior was demonstrated during periods of no-reinforcement except on the initial days of these conditions. The results indicated that a fixed-ratio schedule of reinforcement has certain characteristics capable of producing aggression.     

Remarks on aggression

This paper attempts to draw attention to the difference between the states of mind and inner worlds of neurotic, borderline and psychopathic patients, with reference to different types of destructiveness: anger in the neurotic patient; desperate vengeful hatred in the borderline paranoid; and a cold addiction to violence in the psychopath. Discussion focuses on technical issues and the need to meet the psychopathic patient where he really is, in the inner bleak emotional cemetery he may be inhabiting. Although most patients refuse to stay put in the neat schematic categories outlined, they do seem to appreciate and to need the therapist's recognition of the specific quality of these vastly different states of mind.     

Cholesterol and aggression

Best known for its etiological influence in the cardiovascular disease process, serum cholesterol also plays a role in numerous psychological processes, including affect, cognition, and overt behavior. Prominently, it is related to aggression in humans and other primates. Lipid studies of violent offenders, primary prevention trials of cholesterol reduction, and experimental dietary manipulations in nonhuman primates all point to a significant negative association between cholesterol and physical aggression. By contrast, a positive though inconsistent association between serum cholesterol elevations and verbal aggression (e.g., hostility) has been reported in many studies and often ascribed to a neurophysiological response to acute or chronic stress. We review the numerous studies that have examined the link between serum cholesterol, verbal and physical aggression, and integrate current findings.     

Predatory aggression in lines of wild mice selected for interfemale aggression

Mice descending from lines previously selected for high and low levels of interfemale aggression and from a nonselected control line were exposed to live crickets on two consecutive test days. Latencies both to attack and to eat the cricket were recorded. No line or sex differences in attacking were found, although latency to attack decreased over test days. Control line mice were more likely to engage in the eating of the cricket than either the high or low selected lines, suggesting that the selection procedure may have dissociated attacking and eating components of predatory behavior.     

Components of aggression in chickens and conceptualizations of aggression in general

A refined analysis of the peck order in chickens was offered as a test of the notion that for this species, different responses such as leaping and various types of pecking need not be interchangeable indexes of aggression. Indeed, tests showed that particular response types of the birds were differentially mediated by organismic or environmental factors. In large cages pecking at the body was most frequent by birds that had a home-cage advantage. Contrarily, rates of aggressive leaping were independent of this environmental influence, with males having an advantage over females. Males showed more head pecking than females, but the profile for this sex difference did not resemble the profile for leaping. Correlational analyses revealed that whereas head pecking between testmates was not matched in frequency, leaping was positively related. Finally, the behavior of birds tested in small cages differed from that of the large-cage subjects. Although there was more head pecking in the small cages, males did not have an edge, and leaping was infrequent. Such results indicate that these responses cannot be viewed as interchangeable indicators of aggression in fowl.     

睾酮与人类攻击行为

睾酮是一种可以在男性的睾丸间质细胞、女性卵巢和胎盘的皮层细胞中合成并分泌的雄性激素, 它可以调节个体的各种生理、形态和行为过程, 对个体生存和繁殖至关重要。大量研究表明, 睾酮与社会行为的关联存在双向性, 睾酮可以调节社会行为, 社会行为可以反馈并进一步影响睾酮水平。我们将关注点聚焦于睾酮与人类攻击行为之间的关联。早期研究发现, 高睾酮水平个体表现出更高的攻击性; 近期的研究根据挑战假设理论模型和生物社会地位模型得出, 人体内的睾酮水平对竞争性相互作用具有高度反应性。此外, 通过对大量研究的回顾与分析, 我们总结出睾酮水平的变化可以通过增强杏仁核的反应性或减少前额叶皮质-杏仁核功能耦合来影响攻击行为。未来的研究者应考虑其他激素(如皮质醇)和人格特征调节睾酮和人类攻击行为之间关系的潜在作用, 以及相关的生物学机制。     

The relationship between family aggression history and expressed aggression among college males

The relationship between family of origin aggression and aggression across numerous relationship types was examined among a sample of 197 college‐aged males. Participants completed a self‐report questionnaire assessing the frequency and severity of family aggression (aggression between parents, parental aggression directed toward participants), as well as the frequency and severity of participants' aggression across a number of relationship types (dating, friends, strangers, people in bars, co‐workers, bosses, police officers). The results of the present study indicate that a substantial proportion of college‐aged males report a history of aggressive behavior, both in dating/spousal relationship and other‐relationship types. Analyses revealed that observing parental aggression and receiving aggression from parents was related to aggression in dating relationships. However, only received aggression from parents was related to more general aggressiveness in other non–dating/spousal relationship types. The pattern of findings also suggest that it is important to assess the aggressive behavior of both parents to get a better understanding of the link between family aggression and later expressed aggression. Aggr. Behav. 25:255–267, 1999. © 1999 Wiley‐Liss, Inc.     

Intellectual functioning and aggression

In a 22-year study, data were collected on aggressiveness and intellectual functioning in more than 600 subjects, their parents, and their children. Both aggression and intellectual functioning are reasonably stable in a subject's lifetime and perpetuate themselves across generations and within marriage pairs. Aggression in childhood was shown to interfere with the development of intellectual functioning and to be predictive of poorer intellectual achievement as an adult. Early IQ was related to early subject aggression but did not predict changes in aggression after age 8. On the other hand, differences between early IQ and intellectual achievement in middle adulthood were predictable from early aggressive behavior. A dual-process model was offered to explain the relation between intellectual functioning and aggressive behavior. We hypothesized that low intelligence makes the learning of aggressive responses more likely at an early age, and this aggressive behavior makes continued intellectual development more difficult.