The low male voice is a costly signal of phenotypic quality among Bolivian adolescents

a b s t r a c t a r t i c l e i n f o The human voice is one of the most conspicuous and dimorphic human secondary sexual characteristics; males' low fundamental and formant frequencies barely overlap with females'. Researchers often assert that low male voices are costly signals of phenotypic quality; however, no evidence currently exists linking low voices with indicators of quality (i.e., health or physical condition) during the ages where the larynx develops to adult proportions. In the present study, we examine the relationships between condition, testosterone, and vocal parameters in 91 Bolivian peri-pubertal adolescent males. Condition is operationalized as immune function (based on secretory IgA) and energetic reserves (BMI-for-age residuals from Tsimane-specific growth curves, and body fat percentage), and "masculine" vocal parameters is operationalized as having low fundamental frequency, narrow formant position, and low fundamental-frequency variation. We target peri-pubertal individuals to capture variation in vocal parameters during the canalization period for vocal fold and vocal tract growth. Results indicate that males in better energetic condition have higher testosterone levels and lower voices, controlling for age. Further, testosterone mediates the relationship between condition and a lower voice (i.e., lower fundamental and formant frequencies). We suggest that testosterone plays a key mediating role in the causal pathway linking phenotypic condition to a "masculine" voice. Our results provide support for a costly-signal model of low men's voices

Can listeners assess men's self-reported health from their voice?

Men's voices may provide cues to overall condition; however, little research has assessed whether health status is reliably associated with perceivable voice parameters. In Study 1, we investigated whether listeners could classify voices belonging to men with either relatively lower or higher self-reported health. Participants rated voices for speaker health, disease likelihood, illness frequency, and symptom severity, as well as attractiveness (women only) and dominance (men only). Listeners' were mostly unable to judge the health of male speakers from their voices; however, men rated the voices of men with better self-reported health as sounding more dominant. In Study 2, we tested whether men's vocal parameters (fundamental frequency mean and variation, apparent vocal tract length, and harmonics-to-noise ratio) and aspects of their self-reported health predicted listeners' health and disease resistance ratings of those voices. Speakers' fundamental frequency (ₒ) negatively predicted ratings of health. However, speakers' self-reported health did not predict ratings of health made by listeners. In Study 3, we investigated whether separately manipulating two sexually dimorphic vocal parameters—ₒ and apparent vocal tract length (VTL)—affected listeners' health ratings. Listeners rated men's voices with lower ₒ (but not VTL) as healthier, supporting findings from Study 2. Women rated voices with lower ₒ and VTL as more attractive, and men rated them as more dominant. Thus, while both VTL and ₒ affect dominance and attractiveness judgments, only ₒ appears to affect health judgments. Results of the above studies suggest that, although listeners assign higher health ratings to speakers with more masculine ₒ, these ratings may not be accurate at tracking speakers' self-rated health.Accepted manuscrip

Was facial width-to-height ratio subject to sexual selection pressures? A life course approach

Sexual selection researchers have traditionally focused on adult sex differences; however, the schedule and pattern of sex-specific ontogeny can provide insights unobtainable from an exclusive focus on adults. Recently, it has been debated whether facial width-to-height ratio (fWHR; bi-zygomatic breadth divided by midface height) is a human secondary sexual characteristic (SSC). Here, we review current evidence, then address this debate using ontogenetic evidence, which has been under-explored in fWHR research. Facial measurements were collected from 3D surface images of males and females aged 3 to 40 (Study 1; US European-descent, n = 2449), and from 2D photographs of males and females aged 7 to 21 (Study 2; Bolivian Tsimane, n = 179), which were used to calculate three fWHR variants (which we call fWHRnasion, fWHRstomion, and fWHRbrow) and two other common facial masculinity ratios (facial width-to-lower-face-height ratio, fWHRlower, and cheekbone prominence). We test whether the observed pattern of facial development exhibits patterns indicative of SSCs, i.e., differential adolescent growth in either male or female facial morphology leading to an adult sex difference. Results showed that only fWHRlower exhibited both adult sex differences as well as the classic pattern of ontogeny for SSCs—greater lower-face growth in male adolescents relative to females. fWHRbrow was significantly wider among both pre- and post-pubertal males in the Bolivian Tsimane sample; post-hoc analyses revealed that the effect was driven by large sex differences in brow height, with females having higher placed brows than males across ages. In both samples, all fWHR measures were inversely associated with age; that is, human facial growth is characterized by greater relative elongation in the mid-face and lower face relative to facial width. This trend continues even into middle adulthood. BMI was also a positive predictor of most of the ratios across ages, with greater BMI associated with wider faces. Researchers collecting data on fWHR should target fWHRlower and fWHRbrow and should control for both age and BMI. Researchers should also compare ratio approaches with multivariate techniques, such as geometric morphometrics, to examine whether the latter have greater utility for understanding the evolution of facial sexual dimorphism

Does Men’s Facial Sexual Dimorphism Affect Male Observers’ Selective Attention?

Facial sexual dimorphism affects observers’ physical dominance ratings. Here, we test whether such perceived dominance influences selective attention. To minimize demand characteristics, we examined whether task-irrelevant masculinized men’s faces would show an attentional bias in several experimental paradigms. Experiment 1 employed a Posner Cueing Paradigm in which participants classified shapes after a masculinized or feminized man’s face was presented. We could not find a difference in participants’ classification speeds when either feminized or masculinized face cued target position. Experiment 2 employed a Flanker Task in which participants judged letter orientation, while ignoring flanking faces. There was no observed difference in participants’ reaction time (RT) when masculinized faces flanked the target. Experiment 3 employed a Dot Probe Task, where participants were presented with a masculinized face and a feminized face to the left and right of center screen, and a target shape was presented in the location of one face. Participants’ task was to classify shape orientation. We observe a small effect of facial sexual dimorphism on participants’ classification speed. In Experiment 4, we primed participants with images meant to induce fear or arousal before each trial of a Dot Probe Task. Following the presentation of a fear inducing picture, participants RT to classify shapes when a masculinized face cued target position did not differ from when a feminized face cued target position. The two different presentation times did not create different patterns of results, indicating that masculinized faces did not induce either a cueing or inhibitory affect. Overall, we failed to support the hypothesis that people selectively attend to masculinized faces when they are presented as irrelevant information

Why leveraging sex differences in immune trade‐offs may illuminate the evolution of senescence

The immune system affects senescence (declines in probabilities of survival or reproduction with age), by shaping late age vulnerability to chronic inflammatory diseases and infections. It is also a dynamic interactive system that must balance competing demands across the life course. Thus, immune system function remains an important frontier in understanding the evolution of senescence. Here, we review our expanding mechanistic understanding of immune function over the life course, in the context of theoretical predictions from life-history evolution. We are especially interested in stage- and sex-dependent costs and benefits of investment in the immune system, given differential life-history priorities of the life stages and sexes. We introduce the costs likely to govern immune allocation across the life course. We then discuss theoretical expectations for differences between the sexes and their likely consequences in terms of how the immune system is both modulated by and may modulate senescence, building on information from life-history theory, experimental immunology and demography. We argue that sex differences in immune function provide a potentially powerful probe of selection pressures on the immune system across the life course. In particular, differences in 'competing' and 'caring' between the sexes have evolved across the tree of life, providing repeated instances of divergent selection pressures on immune function occurring within the same overall bauplan. We conclude by detailing an agenda for future research, including development of theoretical predictions of the differences between the sexes under an array of existing models for sex differences in immunity, and empirical tests of such predictions across the tree of life. A free Plain Language Summary can be found within the Supporting Information of this article

SNPs associated with testosterone levels influence human facial morphology

Many factors influence human facial morphology, including genetics, age, nutrition, biomechanical forces, and endocrine factors. Moreover, facial features clearly differ between males and females, and these differences are driven primarily by the influence of sex hormones during growth and development. Specific genetic variants are known to influence circulating sex hormone levels in humans, which we hypothesize, in turn, affect facial features. In this study, we investigated the effects of testosterone-related genetic variants on facial morphology. We tested 32 genetic variants across 22 candidate genes related to levels of testosterone, sex hormone-binding globulin (SHGB) and dehydroepiandrosterone sulfate (DHEAS) in three cohorts of healthy individuals for which 3D facial surface images were available (Pittsburgh 3DFN, Penn State and ALSPAC cohorts; total n = 7418). Facial shape was described using a recently developed extension of the dense-surface correspondence approach, in which the 3D facial surface was partitioned into a set of 63 hierarchically organized modules. Each variant was tested against each of the facial surface modules in a multivariate genetic association-testing framework and meta-analyzed. Additionally, the association between these candidate SNPs and five facial ratios was investigated in the Pittsburgh 3DFN cohort. Two significant associations involving intronic variants of SHBG were found: both rs12150660 (p = 1.07E-07) and rs1799941 (p = 6.15E-06) showed an effect on mandible shape. Rs8023580 (an intronic variant of NR2F2-AS1) showed an association with the total and upper facial width to height ratios (p = 9.61E-04 and p = 7.35E-04, respectively). These results indicate that testosterone-related genetic variants affect normal-range facial morphology, and in particular, facial features known to exhibit strong sexual dimorphism in humans

Different Vocal Parameters Predict Perceptions of Dominance and Attractiveness

Low mean fundamental frequency (F0) in men’s voices has been found to positively influence perceptions of dominance by men and attractiveness by women using standardized speech. Using natural speech obtained during an ecologically valid social interaction, we examined relationships between multiple vocal parameters and dominance and attractiveness judgments. Male voices from an unscripted dating game were judged by men for physical and social dominance and by women in fertile and non-fertile menstrual cycle phases for desirability in short-term and long-term relationships. Five vocal parameters were analyzed: mean F0 (an acoustic correlate of vocal fold size), F0 variation, intensity (loudness), utterance duration, and formant dispersion (Df, an acoustic correlate of vocal tract length). Parallel but separate ratings of speech transcripts served as controls for content. Multiple regression analyses were used to examine the independent contributions of each of the predictors. Physical dominance was predicted by low F0 variation and physically dominant word content. Social dominance was predicted only by socially dominant word content. Ratings of attractiveness by women were predicted by low mean F0, low Df, high intensity, and attractive word content across cycle phase and mating context. Low Df was perceived as attractive by fertile-phase women only. We hypothesize that competitors and potential mates may attend more strongly to different components of men’s voices because of the different types of information these vocal parameters provide

An exploration of the relationships among facial dimensions, age, sex, dominance status and personality in rhesus macaques (Macaca mulatta)

Aspects of personality in nonhuman primates have been linked to health, social relationships, and life history outcomes. In humans as well as nonhuman primates, facial morphology is associated with assertiveness, aggression, and measures of dominance status. In this study we aimed to examine the relationship among facial morphology, age, sex, dominance status, and ratings on the personality dimensions Confidence, Openness, Assertiveness, Friendliness, Activity, and Anxiety in rhesus macaques (Macaca mulatta). We measured facial width-to-height ratio (fWHR) and lower-height/full-height ratio (fLHFH) using photographs from 109 captive rhesus macaques, which observers also assessed for dominance status and personality, and explored the associations among facial morphology, age, sex, dominance status, and personality. fWHR and fLHFH personality associations depended on age category: Assertiveness was associated with higher fWHR and fLHFH, and Confidence was associated with lower fWHR and fLHFH, but all these associations were consistent only in individuals <8 yr. of age. We found fWHR and fLHFH to not be consistently associated with sex or dominance status; compared to younger individuals, we found few associations with fWHR and fLHFH for individuals older than 8 yr., which may be due to limited sample size. Our results indicate that in macaques <8 yr. old, facial morphology is associated with the Assertiveness and Confidence personality dimensions, which is consistent with results suggesting a relationship between fWHR and trait aggression in humans and assertiveness in brown capuchins, all of which implies that fWHR might be a cue to assertive and aggressive traits