Loosening the leash: The unique emotional canvas of human screams.

We use screams to explore ideas presented in the target article. Evolving first in animals as a response to predation, screams reveal more complex social use in nonhuman primates and, in humans, uniquely, are associated with a much greater variety of emotional contexts including fear, anger, surprise, and happiness. This expansion, and the potential for manipulation, promotes listener social vigilance.

Humans read emotional arousal in monkey vocalizations: evidence for evolutionary continuities in communication.

Humans and other mammalian species communicate emotions in ways that reflect evolutionary conservation and continuity, an observation first made by Darwin. One approach to testing this hypothesis has been to assess the capacity to perceive the emotional content of the vocalizations of other species. Using a binary forced choice task, we tested perception of the emotional intensity represented in coos and screams of infant and juvenile female rhesus macaques () by 113 human listeners without, and 12 listeners with, experience (as researchers or care technicians) with this species.

Vocal expression of emotional arousal across two call types in young rhesus macaques.

As Darwin first recognized, the study of emotional communication has the potential to improve scientific understanding of the mechanisms of signal production as well as how signals evolve. We examined the relationships between emotional arousal and selected acoustic characteristics of coo and scream vocalizations produced by female rhesus macaques, , during development. For coos, arousal was assessed through measures of stress-induced elevations of plasma cortisol exhibited in response to the human intruder test.

When less is more in the evolution of language.

Did loss of vocal fold membranes typical of nonhuman primates enable human speech?

The emotional canvas of human screams: patterns and acoustic cues in the perceptual categorization of a basic call type.

Screams occur across taxonomically widespread species, typically in antipredator situations, and are strikingly similar acoustically, but in nonhuman primates, they have taken on acoustically varied forms in association with more contextually complex functions related to agonistic recruitment. Humans scream in an even broader range of contexts, but the extent to which acoustic variation allows listeners to perceive different emotional meanings remains unknown. We investigated how listeners responded to 30 contextually diverse human screams on six different emotion prompts as well as how selected acoustic cues predicted these responses.

Do human screams permit individual recognition?

The recognition of individuals through vocalizations is a highly adaptive ability in the social behavior of many species, including humans. However, the extent to which nonlinguistic vocalizations such as screams permit individual recognition in humans remains unclear. Using a same-different vocalizer discrimination task, we investigated participants' ability to correctly identify whether pairs of screams were produced by the same person or two different people, a critical prerequisite to individual recognition.

The credibility of acted screams: Implications for emotional communication research.

Researchers have long relied on acted material to study emotional expression and perception in humans. It has been suggested, however, that certain aspects of natural expressions are difficult or impossible to produce voluntarily outside of their associated emotional contexts, and that acted expressions tend to be overly intense caricatures. From an evolutionary perspective, listeners' abilities to distinguish acted from natural expressions likely depend on the type of expression in question, the costs entailed in its production, and elements of receiver psychology.

Behavioral and genetic correlates of the neural response to infant crying among human fathers.

Although evolution has shaped human infant crying and the corresponding response from caregivers, there is marked variation in paternal involvement and caretaking behavior, highlighting the importance of understanding the neurobiology supporting optimal paternal responses to cries. We explored the neural response to infant cries in fathers of children aged 1-2, and its relationship with hormone levels, variation in the androgen receptor (AR) gene, parental attitudes and parental behavior. Although number of AR CAG trinucleotide repeats was positively correlated with neural activity in brain regions important for empathy (anterior insula and inferior frontal gyrus), restrictive attitudes were inversely correlated with neural activity in these regions and with regions involved with emotion regulation (orbitofrontal cortex).

Reading chimpanzee faces: evidence for the role of verbal labels in categorical perception of emotion.

Categorical perception (CP) occurs when continuously varying stimuli are perceived as belonging to discrete categories. Thereby, perceivers are more accurate at discriminating between stimuli of different categories than between stimuli within the same category (Harnad, 1987; Goldstone, 1994). The current experiments investigated whether the structural information in the face is sufficient for CP to occur.

Recognition of rhesus macaque (Macaca mulatta) noisy screams: evidence from conspecifics and human listeners.

Vocalizations are among the diverse cues that animals use to recognize individual conspecifics. For some calls, such as noisy screams, there is debate over whether such recognition occurs. To test recognition of rhesus macaque noisy screams, recorded calls were played back to unrelated and related conspecific group members as either single calls or short bouts.

Sex differences in juvenile rhesus macaque (Macaca mulatta) agonistic screams: life history differences and effects of prenatal androgens.

This study investigated sex differences in juvenile rhesus macaque (Macaca mulatta) vocal behavior during agonistic contexts, and the effects of prenatal androgens on these differences. A total of 59 subjects (5-8 per treatment group) received exogenous androgen (testosterone enanthate), an anti-androgen (flutamide) or vehicle injections (DMSO) for 30 or 35 days during the second (early) or third (late) trimester of pregnancy. An additional 19 unmanipulated controls were included in the analysis.

Sex differences in the acquisition of communicative competence by pigtail macaques (Macaca nemestrina).

Previous study of captive pigtail monkeys (Macaca nemestrina) revealed that victims of an attack by a group member employed one of four acoustically different recruitment calls (Gouzoules&Gouzoules: Animal Behaviour 37:383-401, 1989). The calls appear to provide allies with information pertinent to decisions about fight intervention. Each call was associated with an agonistic context distinguished by the relative rank of the opponent and the severity of the attack.

Physiological and social influences on mounting behavior of troop-living female monkeys (Macaca fuscata).

Female mounting behavior was studied in a troop of Japanese macaques during one breeding season. Of 79 sexually active females, mounting behavior during consortships was shown by 50 females; 13 only with males, 20 with both males and females, and 17 only with females. Several factors associated with reproductive state influenced the expression of mounting activity.