Decreased Sexual Motivation during the Human Implantation Window

– by James R. Roney

A lot of research has investigated shifts in women’s psychology and behavior across different phases of the menstrual cycle. One pattern that has emerged in multiple studies is an increase in sexual desire during the “fertile window,” which is defined as the cycle days when unprotected intercourse can lead to conception. In humans, the fertile window extends from about 5 days before ovulation through the day of ovulation itself, with the ovulation day usually falling near the mid-point of a typical menstrual cycle.

Why should desire go up during the fertile window? Motivational priorities theory argues that hormonal signals tend to increase sexual motivation when the net fitness benefits of sex were highest during human evolution. Fitness benefits were outcomes associated with increased gene replication, whereas fitness costs were outcomes associated with decreased gene replication; net benefits were benefits minus costs. Sex would have had fitness costs for our female ancestors: it could have caused injury, infection, social disapproval from competitors, or just distraction from other behaviors. Conception would have been a fitness benefit from sex: indeed, gene replication is not possible without it. Because conception was possible only during the fertile window, however, there was an increase in the benefit side of the fitness equation during the fertile window that may have acted as a selection pressure to increase sexual motivation at that time.

This simple cost-benefit analysis may explain why most of the evolutionary literature on menstrual cycle shifts—including my own research—has focused primarily on the fertile window. But what if certain fitness costs of sex were not constant across the cycle, as perhaps generally assumed, but instead increased during specific time windows? My co-authors and I explored that possibility, reasoning that increased infection risk during the “implantation window” may have selected for reduced sexual motivation at that time.

The implantation window refers to those days when the endometrium (the uterine lining) is receptive to attachment by an embryo. (The image at the top of this post illustrates the attachment process.) Part of being receptive entails a reduction of immune responses within the uterus to prevent the immune system from attacking an embryo if conception has occurred. However, that same immunosuppression may make women more vulnerable to sexually transmitted infections (STIs) at this time. As reviewed in our article, progesterone appears to be a key signal that helps to cause such immunosuppression, and both experiments in nonhuman species and correlational research in humans supports increased susceptibility to some types of STIs when progesterone is elevated. That increased infection risk should have increased the cost side of the benefits minus costs fitness equation during the implantation window, thus acting as a selection pressure to reduce sexual motivation at that time.

Based on the above reasoning, we tested whether measures of women’s sexual motivation were lower during the estimated implantation window. The implantation window is estimated to run from about 5 to 9 days after ovulation in humans, during an infertile region of the cycle called the luteal phase. We used data from three daily diary studies that had previously been conducted in my lab. In each study, women responded to daily online surveys across full menstrual cycles. The surveys included measures of subjective sexual desire and reports of whether women masturbated, which were chosen as our primary measures of sexual motivation. Hormonal estimates of the day of ovulation were also available in each study; by counting forward from the day of ovulation, we could estimate the implantation window days within each cycle.

Across the three studies, there were 2576 survey responses across 102 ovulatory menstrual cycles sampled from 83 women. Our data analyses used statistical techniques to estimate, within the same women, whether responses differed on implantation window days relative to other cycle regions. (Imagine, for instance, for one woman, subtracting her average desire during the implantation window from her desire on all other days, and then averaging that difference across all women; our multi-level regression models made conceptually analogous comparisons.)

Our results provided evidence for lower self-reported sexual desire during the implantation window relative to the remaining days of the cycle. This was true in each of the three studies and also in the combined sample. Importantly, desire in the combined sample was lower in the implantation window relative to cycle regions that excluded days within the fertile window. That result demonstrates that lower desire during the implantation window was not simply an artifact of comparisons with elevated desire during the fertile window. Results for our behavioral measure of sexual motivation were slightly less clear, perhaps because about 40% of our sample reported no incidents of masturbation. Nonetheless, in the combined sample, there were one-third lower odds of masturbation during the implantation window relative to all other cycle days.

These findings add a new wrinkle to research on cycle phase shifts in women’s sexuality. Hormonal mechanisms may generate changes in sexual motivation within two conceptually significant windows of time: increased desire within the fertile window when conception is possible, and decreased desire during the implantation window when infection risk is elevated. There may be alternative explanations for why desire is reduced during the implantation window—some of which we considered in our article—and we hope these findings encourage further research into whether there are adaptations that modulate sexual motivation based on implantation window timing.

Roney, J. R., Simmons, Z. L., Mei, M., Grillot, R. L., & Emery Thompson, M. (2025). Decreased sexual motivation during the human implantation window. Evolution and Human Behavior, 46, 106761.

Agent-based simulations of the evolution of psychopathy

– by Dražen Domijan

Agent-based simulations offer valuable insights into processes that are difficult or impossible to observe directly. They enable systematic variation of relevant factors and examination of their influence on the behavior of simulated agents. For example, one can examine and compare how the same trait evolves under favorable conditions in an environment with abundant resources, or in a harsh environment where resources to sustain life are scarce. In this work, we were inspired by a recently developed agent-based model by Dr. Martina Testori and her colleagues. We are grateful to Dr. Testori for openly sharing their simulation code, which increases the transparency and reproducibility of computational studies and also significantly reduces the time required to develop our extended model.

Testori et al. adopted a public goods game in which generous and selfish agents interact to produce resources that are shared equally among all members of the society. Agents then reproduce and are replaced by their offspring in the next generation. The number of offspring each parent produces is proportional to their fitness. If an agent’s fitness is below the survival threshold, the agent dies without leaving offspring. Reproduction is governed by a probabilistic mechanism that incorporates genetic propensity for selfishness and behavioral contribution to the development of selfish and generous personality traits. This mechanism enables offspring to inherit their parents’ phenotype or to switch to the opposite phenotype with a certain probability of mutation.

To simulate psychopathic traits in more detail, Testori et al. introduced two additional behavioral components of the psychopathic personality, beyond mere selfishness. Firstly, psychopathic individuals tend to engage in risky behaviors that may lead to their premature deaths and removal from society. In the model, this is represented by a parameter called the mortality rate, meaning that a fraction of psychopaths were eliminated from the game before they had the opportunity to reproduce. Secondly, psychopathic individuals tend to engage in destructive acts that harm public goods, thereby imposing a community cost on available resources. The mortality rate and community cost are free parameters that are allowed to vary independently, enabling their effects on the evolution of psychopathy to be assessed in simulations.

When we began work on this project, our attention was immediately drawn to the finding that, in most reported simulations in the Testori et al. study, selfish agents dominated society. In some combinations of mortality rate and community cost, they constitute more than 80% of the population. However, this is not a plausible evolutionary outcome, as a recent meta-analysis suggests that the frequency of psychopaths in the human population is quite low. Estimates range from 1.2% to 4.5%, depending on the instrument used to assess psychopathy. Some authors even suggest a more conservative estimate of around 1% in the general population. This raises an important question: what societal forces keep the fraction of psychopathic individuals at such low levels?

Inspired by the work of Hiroaki Chiba-Okabe and Joshua Plotkin, we hypothesized that institutions could serve as a stabilizing factor that alleviate the adverse consequences of the actions of selfish agents. Here, institution should be understood in the broadest sense, involving any set of rules that regulate interactions among members of a society. In our model, the role of the institution is to act as an external agent that partially reallocates resources from psychopathic agents to cooperators, thus helping to reduce the resource inequality generated in the public goods game. In this way, the institution increases the fitness of generous agents who are disadvantaged in exchanges with selfish agents. We devised several scenarios in which the institution imposes punishment on selfish agents, or combines punishment of selfish agents with rewards for generous agents. We also considered the effect of conditional cooperation, that is, a scenario in which cooperators adjust their contributions to the public goods game by taking into account information about the level of cooperation in the previous generation.

Our simulations showed that both punishing selfish agents and rewarding generous agents were necessary to reduce the proportion of selfish agents in society to levels closer  to those observed empirically. Furthermore, these measures must be accompanied by a high mortality rate among selfish agents. However, although we approached our target, we were unable to achieve exactly 1% selfish agents in the final population. Our results suggest that selfish agents are highly resistant and manage to survive institutional interventions. This supports the conclusion that psychopathy may have adaptive value because it strongly contributes to fitness. This is consistent with several recent studies showing that certain features of psychopathy, especially manipulation and emotional coldness, are positively associated with fertility as a crucial component of evolutionary fitness. Interestingly, across simulations we also observed that population size increases as institutional interventions become stronger. Thus, institutional redistribution of resources contributes to population growth.

To keep our model as simple as possible, we made several simplifications and left many topics unaddressed. For example, we treated personality traits as if they were consistent with genetic makeup. However, it is possible that psychopaths alter their behavior in situations where psychopathic behavior is punished or prosocial behavior is rewarded. We modeled psychopathy as a single phenotype, although it is better described as a behavioral syndrome that can be subdivided into several distinct phenotypes. We also kept the environment constant across generations, although it may fluctuate over time. We hope our work will inspire further computational explorations of the societal and ecological conditions that shape the evolution of psychopathy.

Dražen Domijan & Janko Međedović. (2026). Evolution of psychopathy in the public goods game with institutional redistribution of resources. Evolution & Human Behavior, 47, 106771.

Engineering Fear: Protagonist Vulnerability and the Evolutionary Design of Horror

– by Edgar Dubourg and Coltan Scrivner

What is it about some stories and situations that make them more effective at evoking fear? One way to answer this is to reverse engineer the emotion of fear.

Our ancestors would have come across a number of hostile people and animals throughout their lives. Quickly computing the odds of survival in the event of a conflict would have been an extremely valuable cognitive ability. The score for each side’s ability to win an all out fight has been conceptualized as formidability and has been successfully applied to understand emotions like anger. We argue that formidability may also help us understand the emotion of fear. Perceiving an adversary whose formidability far outmatches your own should trigger a computational appraisal of poor survival odds, perhaps felt as vulnerability. Fear should be one output of that appraisal, helping to coordinate defensive attention, arousal, and avoidance. Given this, stories that present a formidability asymmetry between the hero and villain such that the villain is powerful and the hero is weaker and more vulnerable should be better at evoking fear.

Horror fiction is the genre most closely associated with the emotion of fear — so much so, that the ability and intent to scare the audience is often found in definitions of the genre. If our hypothesis about formidability asymmetry and fear is correct, then the basic format of a horror story should be a powerful antagonist facing a vulnerable protagonist.

According to this hypothesis, it’s not only a weak protagonist or only a powerful antagonist that makes a story horrifying. Rather, it is the overall vulnerability of the protagonist. In Alien, (1979), a nearly perfect extraterrestrial predator stalking a commercial spaceship crew produces sustained fear because the crew is unprepared, poorly armed, and trapped, with limited information and no reliable escape. Predator (1987) presents a similarly powerful and predatory antagonist stalking a group of people. However, this group of people are an elite paramilitary team led by a character who is portrayed by former Mr. Universe, Arnold Schwarzenegger. As a result of the powerful protagonists, Predator feels much more like an action movie than a horror movie. For the same reason, superhero movies that feature powerful antagonists and loads of violence typically feel more like action rather than horror. Likewise, many films with low-formidability protagonists (e.g., Kevin from Home Alone) can end up in the comedy realm when the antagonists are also low formidability.

To test this hypothesis at scale, we relied on an automated annotation method that leverages the latent cultural knowledge of large language models. Rather than manually coding films one by one, we used a structured prompting procedure to have a language model estimate key narrative features for each movie, such as the formidability of both the protagonist and antagonist, the persistence of the threat, and the hostility of the environment.

Analyzing 691 films spanning ten broad film genres including horror, action, thriller, fantasy, and romance, we found a clear structural partition. Horror films were uniquely characterized by weak protagonists, strong antagonists, persistent threats, and hostile environments. Action, fantasy and thriller films, by contrast, often featured formidable antagonists but paired them with capable or well-equipped protagonists, resulting in much lower protagonist vulnerability. In other words, what separates horror from other genres is not the presence of danger, but the systematic imbalance between who threatens and who must endure the threat.

This raised a natural follow-up question: does protagonist vulnerability predict fear even outside the horror genre? To address this, we turned to viewer-generated data. Among films not labeled as horror, some are nonetheless widely described as frightening. Using IMDb’s keyword system, we compared non-horror movies that were tagged with fear-related terms to those that were not. The result was strikingly consistent: non-horror films associated with fear keywords showed significantly higher vulnerability scores. This suggests that the same structural ingredients that define horror also predict fear at a finer narrative level, beyond genre labels themselves.

Finally, we asked whether protagonist vulnerability tracks not just perceived fear, but also its associated physiological responses. Using data from an independent project that measured viewers’ heart rates while watching horror films, we found that horror movies with higher vulnerability scores reliably elicited stronger increases in heart rate. In short, narratives that place weak protagonists in the path of overwhelming threats engage the body’s threat-management systems more intensely.  All these tests held even when accounting for the film’s release year and remained robust across alternative ways of computing protagonist vulnerability.

Together, these findings, reported in Evolution and Human Behavior, show that protagonist vulnerability captures a core input condition of fear in movies across genre boundaries, subjective judgments, and physiological responses. More generally, this perspective helps explain why certain narrative tropes recur so reliably in horror fiction. Characters in horror films are isolated, cut off from communication, or trapped in hostile environments because isolation removes social and material resources that would otherwise reduce vulnerability. Settings such as remote cabins, deserted hotels, confined spaces, or unfamiliar worlds systematically limit escape and amplify exposure to harm. Even when protagonists are adults, horror often strips them of weapons, authority, or knowledge, placing them in situations where resistance is ineffective and outcomes feel uncontrollable. From this perspective, many classic ingredients of horror such as darkness, confinement, isolation, helplessness, are efficient ways of engineering vulnerability.

More broadly, these results shed light on how the fear system is elicited. They suggest that fear is not triggered simply by the detection of threat-related cues, but by an assessment of whether harm is plausible given the situation and capacities of the individual facing the threat. Horror fiction is particularly well suited to revealing these input conditions because it systematically exaggerates and isolates them. By holding constant the nature of the threat while varying the vulnerability of protagonists, fictional narratives create controlled contrasts that would be difficult or unethical to study in real life. More generally, cultural products that are explicitly designed to evoke specific emotions provide a powerful and efficient way to study the input conditions of evolved psychological mechanisms: when they succeed across audiences and contexts, they offer converging evidence about how those mechanisms are tuned to the structure of the world.

Edgard Dubourg & Coltan Scrivner. (2026). Vulnerability and the computational logic of fear: insights from the horror genre. Evolution & Human Behavior, 47, 106813.

Is He a Good Dad, or Does He Just Have His Mother’s Genes?

– by Thomas Felesina

The male nipple is a classic conversation starter (at least in the evo biology faculty lounge). The nipple is a feature that is functional and essential for reproductive success in females,[1] yet non-functional in males, perhaps decorative at best. We don’t spend much time agonizing over the “evolutionary function” of the male nipple. We generally accept that it exists not because it provides a fitness advantage to men, but because men and women are built from the same genetic blueprint. Men have nipples because women need them, and decoupling the genetic architecture for chest anatomy between the sexes is evolutionarily “expensive” and largely unnecessary since it imposes few costs for men. To get rid of male nipples, a mutation would first need to occur that says something like, “grow nipples ONLY if female” or “suppress nipples ONLY if male.”

However, when we move from anatomy to psychology and behavior, we often lose sight of this logic: forgetting that the shared genome governing the male and female body also governs the male and female mind. We have 23 pairs of chromosomes. Aside from the sex chromosomes (X and Y), the other 22 pairs, the autosomes, are effectively identical between the sexes. This means that most genetic variants that influence our brains and our behavior are the same for both males and females.

In my recent paper, I show that for many complex traits, the genetic correlation between the sexes (referred to as rMF) is extremely high. The genetic correlation is extremely high because when sharing genetic architecture, you cannot easily pull one sex in an evolutionary direction without dragging the other sex along with it (referred to as a correlated response). Consequently, when selection favors a trait in females, the mean trait value may increase in males as well, even if it provides no direct benefit or is slightly costly. This is the genetic equivalent of a sidecar on a motorcycle: if the driver (the sex under strong selection) turns left, the passenger (the other sex) goes left, too.

And so, when we ignore the correlated responses to selection acting on one sex, we risk falling into a trap of proposing two separate adaptive explanations: one for men, and one for women, when a single explanation might do, or at the very least, be a significant factor in the initial evolution of a trait in one of the sexes.

For instance, evolutionary psychology emphasizes that females should be “choosy” because the biological costs of a bad mating decision are high (e.g., expensive eggs, pregnancy, lactation). Males, with lower obligatory investment, are theoretically predicted (and empirically observed among many animals) to be less choosy. Yet, human men are surprisingly discriminating compared to most male mammals. Is this because men faced their own unique selection pressures to be picky? Perhaps. But it is arguably more parsimonious to suggest that strong selection for choosiness in women, driven by prolonged child-rearing demands, shifted male psychology in the same direction via our shared genome.

Take another example: humans are outliers among mammals; our fathers are unusually involved in child-rearing. Perhaps paternal care in humans increased offspring survival or improved mating opportunities, but it would be remiss to ignore the selective pressure on human mothers to be nurturing and attentive to highly dependent, altricial infants. Natural selection would have aggressively favored genetic variants that promoted responsiveness to infant cues, patience, and bonding in mothers. Because these “parental” genes likely reside on the autosomes, they are inherited by sons just as they are by daughters, leading to the emergence of paternal care. And so, the baseline capacity for human paternal care may be, at least initially, a genetic byproduct of intense selection on maternal care. Men may be nurturing dads partly because they are the sons of nurturing mothers.

While my review of the quantitative genetic literature found that high genetic correlations (often nearing 1.0) are the norm for human behavior, there are, of course, exceptions. For instance, research on extra-pair mating (infidelity) in humans has shown a surprisingly low genetic correlation between the sexes. This suggests that for cheating behavior, men and women may indeed have evolved under distinct, sex-specific pressures, allowing their genetic architectures to decouple.

Why This Matters for the Future of the Field

Acknowledging the shared genome doesn’t mean denying sex differences. Men and women differ significantly in height, yet the genetic correlation between the sexes for height is near-perfect. As I discuss in the paper, while the set of genes influencing a trait is largely the same for both sexes, the magnitude of their effect can differ for a variety of reasons; for instance, the distinct hormonal environments of men and women can amplify or dampen the effect of genes.

With this in mind, as evolutionary social scientists, we should adopt a new default assumption: unless we have evidence to the contrary, we should assume the genetic correlation between sexes is high. To claim that a trait evolved independently in both men and women requires us to devise two separate adaptive accounts, one for each sex, while also assuming the successful evolution of complex mechanisms to decouple their genetics. In contrast, assuming a high genetic correlation requires only one adaptive explanation: selection acted strongly on one sex, and the other simply inherited the trait. The latter explanation demands fewer assumptions, aligns with the biological reality of our shared genome, and should therefore be our starting point.

By respecting the constraints of our shared DNA, we can build more rigorous, parsimonious, and biologically grounded theories of human behavior. Sometimes, a dad is a dad because he evolved to be one. But sometimes, he’s a dad because his mother was a mom.

[1] While the functional nipple is a female trait, it is essential for the reproductive success of both sexes.

Thomas Felesina. (2026). The shared genome constraint: why between-sex genetic correlation matters for evolutionary social science. Evolution & Human Behavior, 47, 106773.

Gender differences in social networks under subsistence changes

– by Juan Du

Quick question: If something went wrong tonight and you needed help fast—someone to watch a child, lend money, give you a ride—who comes to mind first: a friend, your own family, or your partner’s family? And if you asked your partner, would they choose the same side? People sometimes tease that men have an endless supply of “brother dinners”, while women seem to keep a smaller circle—but hold onto it tightly. It’s easy to shrug and say “that’s just gender” or “that’s just culture”. But our new paper suggests those patterns aren’t fixed and there are gendered differences.

Instead of asking whether men and women are “naturally” different, we asked what happens to social relationships when the rules of everyday life change? In particular, what happens when a community shifts from mainly farming and herding toward deeper involvement in markets—more wage work, more trading, more travel, more time pressure?

We understand that relationships are not just “social”. They are how people get labor help, childcare support, information, and backup when things go wrong. But maintaining relationships takes time. And time is the one resource that becomes painfully scarce as market life expands. The basic idea is that not all social ties cost the same to maintain. In our paper, we focus on two types of relationship: friendship and kinship.

You may able to list a few friends in your daily life, but it is hard to say whether you will keep your friends the same during your lifetime. And, as you grow older, you find that maintaining friendships become even more difficult. Thus friendships become incredibly valuable and expensive. You don’t keep friendships strong by accident—you keep them strong by showing up.

Whereas kin ties can work differently. In many rural settings, cooperation among relatives is woven into everyday routines: shared labor work, shared responsibilities, shared obligations, and the kind of long-term accounting that doesn’t reset every time you miss a meal together. That doesn’t mean kin ties are always easy or conflict-free, but they can be harder to “drop” and sometimes more resilient when time is tight.

So when market participation increases, we expected a simple trade-off to intensify: friendship becomes more expensive; kin cooperation may become a safer bet.

And because market work and mobility often change more for men than for women in many settings, we also expected something else: men’s networks might be reshaped more strongly by market involvement, while women’s networks might remain steadier. Not because women are “born stable,” but because women’s daily cooperative demands—childcare, household coordination, local mutual aid—may stay locally focused even as markets expand.

We worked in a Tibetan community in the Shangri-La region of Yunnan, where economic life has been shifting quickly from traditional farming and herding subsistence to more market involved. Our dataset comes from more than a decade of cumulative research across 14 villages. We collected detailed information on 1,169 married adults, focusing on their core social interactions.

We separated these relationships into four types:

  • the person’s overall core network
  • biological kin
  • in-laws (affinal kin)
  • friends (non-kin)

And we used a simple structural measure—network density—to capture whether someone’s close ties form a tightly connected cluster or a looser set. Dense networks can be a sign of coordinated support: people know each other, information travels fast, and cooperation can be reinforced through reputation and mutual monitoring.

We found that among men, higher market participation went with a shift away from friends and toward kin. As men became more engaged in market activities, their kin networks became more cohesive, while friend networks became less cohesive.

This is not the same as saying “men lose friends.” What we see looks more like reallocation. When time and movement are squeezed, men appear to concentrate social effort on relationships that are more durable and more predictably cooperative. If showing up frequently becomes hard, friendship—especially the kind built on frequent contact—may be the first thing to thin out.

Women’s networks, looked comparatively stable across market involvement. Women maintained dense, high-quality core ties regardless of whether they were more or less involved in market activities. The most plausible explanation is not that women are “just better at relationships,” but that women’s roles and cooperative needs remain more locally embedded: if you are coordinating childcare, household work, and everyday mutual help, you cannot afford to let your support network drift.

We also looked at post-marital residence—whether people live near their own family or near their spouse’s family affects their relationships. This matters because residence literally determines who is within reach for daily cooperation. And we found that:

  • if you live near your natal kin, your biological-kin network is stronger;
  • if you live near your spouse’s side, your in-law network becomes stronger.

That might sound obvious, but it implied that in-laws can operate as real cooperative partners, not merely “secondary” ties. When biological kin are less accessible, affinal kin can step in and support a bilateral cooperative network—a support system sustained by both sides of the family rather than only one lineage line.

So yes, you can still recognize the old pattern—men with lots of social occasions, women with steadier core ties. But what matters is how that pattern moves when work starts pulling people around and evenings disappear. In this community, the changes were clear: as time and mobility constraints grew, men and women reorganized which relationships they kept warm, and which ones were allowed to cool.

Yaming Huang, Gabriel Šaffa, Shiting Zhang, Pengpeng Bai, Liqiong Zhou, Gui He, Ruth Mace, & Juan Du. (2026). Gender differences in social networks under subsistence changes. Evolution & Human Behaviuor, 47, 106814.

When Faces Fall Out of Sync: What Bonobo Sex Tells Us About the Evolution of Nonverbal Communication

– by Martina Francesconi & Elisabetta Palagi

Sex is often thought of as a purely physical activity, driven by movements, touch, and physiological arousal. Yet in humans, sexual interactions are also deeply communicative. Eye contact, facial expressions, and subtle emotional cues shape how partners experience intimacy, influencing feelings of pleasure, connection, and satisfaction. Nonverbal communication, in particular, appears to play a central role: during sex, faces and bodies often “speak” more loudly than words.

But are these communicative dimensions of sexuality uniquely human? Or do they have deeper evolutionary roots?

To explore this question, we turned to one of our closest living relatives: the bonobo (Pan paniscus). Bonobos are famous for their rich sexual repertoire. Unlike most other primates, they engage in sexual interactions across ages and sexes, and not only for reproduction. Sex in bonobos also serves important social functions, helping to reduce tension, repair relationships, and strengthen social bonds. This makes them an ideal model species for investigating the evolutionary origins of sexual communication.

In humans, facial expressions during sex are often interpreted as spontaneous manifestations of pleasure. Yet growing evidence suggests that they may also play an active communicative role, helping partners coordinate emotionally and behaviorally. Testing this idea directly in humans is extremely difficult for obvious ethical and practical reasons. In non-human primates, observing spontaneous sexual interactions with fine-grained temporal precision is simply not feasible. Bonobos offer a rare opportunity to overcome this limitation. Their sexual interactions are frequent, often face-to-face, and occur in a social context where detailed behavioral observation is possible. Importantly, bonobos regularly display a facial expression known as the silent bared-teeth display (SBT) during sex. This expression can be produced by one partner alone, or reciprocated by both partners in a rapid, automatic exchange known as Rapid Facial Mimicry (RFM), where one individual mirrors the other’s facial expression within less than a second.

This distinction allowed us to ask a key question: is it simply seeing a partner’s facial expression that matters during sex, or is it the mutual exchange, the moment when both partners’ faces fall into synchrony?

To address this question, we analyzed sexual interactions in a captive bonobo colony using high-resolution video recordings. Rather than focusing on outcomes such as mating success, we examined the moment-to-moment dynamics of sexual interactions. Specifically, we used the rate of rhythmic pelvic or genital movements as a proxy for the intensity of sexual stimulation. Faster, more frequent movements indicate higher levels of stimulation, while slower rates suggest a decline. We then examined how these movement patterns changed before, during, and after different facial expression conditions: no facial expressions, unilateral SBTs, and reciprocal facial mimicry (RFM). Crucially, our analyses focused not just on whether these behaviors co-occurred, but on timing. We asked what happens immediately when facial mimicry begins, and what happens when it ends.

Our results revealed a striking pattern. Sexual interactions involving rapid facial mimicry were characterized by the highest levels of stimulation. When both partners mirrored each other’s facial expressions, the rate of rhythmic movements reached a peak. Even more telling was what happened when this mimicry stopped. As soon as facial synchrony was disrupted, when even one partner ceased to mirror the other, the intensity of sexual stimulation sharply dropped. This decline occurred rapidly, within seconds, and persisted even when we excluded interactions interrupted by third parties or external disturbances.

By contrast, unilateral facial expressions told a different story. When only one partner displayed the silent bared-teeth expression, without being mimicked, stimulation levels did not show a consistent or robust change. In other words, expressing a facial signal was not enough. What mattered was sharing it.

These findings suggest that rapid facial mimicry does not merely reflect pleasure as a byproduct of sexual stimulation. Instead, it appears to mark moments of fine-grained socio-emotional coordination between partners.

One possible interpretation was that facial mimicry might serve as an anticipatory signal, communicating motivation to increase stimulation. However, our data did not support this idea. Stimulation did not increase after facial mimicry occurred. Rather, it was highest during mimicry and declined immediately once it ended. This pattern indicates that RFM marks the peak of sexual coordination rather than signaling a future escalation. In short, when partners are emotionally and behaviorally aligned, stimulation is highest; when facial synchrony breaks down, so does intensity. Whether these peaks in stimulation correspond to orgasm or other reward states remains an open question. Nonetheless, our findings have broader implications. Rapid facial mimicry is observed in bonobos across multiple social contexts, including social play, and is thought to reflect shared emotional states and automatic emotional resonance.

Our study suggests that such facial coordination mechanisms may also play a role in regulating sexual interactions. Given the importance of sex in bonobo social life, not only for reproduction but also for maintaining tolerance, cooperation, and social bonds, selection may have favored individuals who could finely tune their behavior to their partners’ emotional signals.

From an evolutionary perspective, this points to a deep-rooted link between nonverbal communication, emotional synchrony, and coordinated social action. The communicative role of facial expressions during human sexual interactions may therefore not be a recent cultural invention, but part of an ancient primate toolkit for social connection.

In both bonobos and humans, it seems that during intimate moments, being in sync matters as much as, if not more than, the movements themselves.

Martina Francesconi, Alice Galotti, Yannick Jadoul, Federico Giovannini, Andrea Ravignani, & Elisabetta Palagi. (2026) SEX in bonobos: The intensity of sexual stimulation sharply drops after facial mimicry. Evolution & Human Behavior, 47, 106786.

Share your thoughts on the future of HBES

The Future of HBES Committee was formed to identify key challenges and opportunities facing the Human Behavior and Evolution Society, and to develop strategies to ensure that HBES remains the intellectual home for scholars of evolutionary behavioral science. As part of this effort, we will be holding several small focus groups to hear perspectives from a broad range of voices within our field and the society.

Click here if you like to participate in one of these focus groups.

Postdoctoral Researcher Positions in Psychology, Cognitive Science, Anthropology, or Related Disciplines – Tolouse School of Economics

The Department of Social and Behavioral Sciences (SBS) at the Toulouse School of Economics (TSE) offers jobs for Postdoctoral Researchers with a PhD in psychology, cognitive science, anthropology, or related disciplines.

Two 2-year positions, fully based in Toulouse (fixed-term contract; full-time basis)
Starting date: September 2026 and deadline for application: January 23, 2026

For more information, visit the website.

I thought we were just friends! Emergence of Sexual Misperception Biases in Adolescence

– by Marius Stavang

Imagine you’re on a movie date with someone. Everything seems to be going great. The conversation flows easily, you laugh together, you exchange smiles—there’s chemistry. After the movie, you walk them home. On their doorstep, you exchange a lingering look and a shared laugh about how good—or bad—the movie was. The moment feels perfect. There are sparks. Nervous, but summoning what courage you can, you close your eyes, purse your lips, and lean in for a kiss.

Suddenly you’re interrupted with a loud protest, “I thought we were just friends!”  Your heart sinks immediately, you feel devastated, crushed, and also—deeply ashamed. You realize you’ve misinterpreted the relationship between the two of you. You mistook their friendliness for romantic interest. Meanwhile, your friend—confused and saddened by what’s happening—feels their own sting of guilt and embarrassment. How could they not have seen that your invitation might have meant something more?

In evolutionary psychology, these two errors of inference are referred to as sexual overperception and sexual underperception. Sexual overperception involves mistaking someone’s friendliness for romantic interest, whereas sexual underperception involves mistaking romantic interest for mere friendliness.

If people were always completely transparent about their romantic interest—“Hey, I fancy you as a long-term romantic partner. Want to go see a movie together?”—errors in sexual perception wouldn’t occur. But for some reason humans are highly anxious and cautious about revealing their non-platonic interest. Instead, we engage in a subtle dance, gradually signaling that we want “something more,” while trying to infer whether the other person is spending time with us for the same reason. And because humans are imperfect mind readers, errors in sexual inference are inevitable.

It also turns out that men and women are not equally likely to sexually over- or underperceive one another. A large body of research shows that men are more likely to overperceive women’s interest than to underperceive it, whereas women are more likely to underperceive men’s interest than to overperceive it. The magnitude and consistency of these sex differences have led researchers to label them the male sexual overperception bias and the female sexual underperception bias.

Put simply, men tend to overestimate how keen women are on them, while women tend to underestimate how keen men are on them. These sexual misperception biases have been identified consistently in adults across a wide range of methods. But an important question remains: When do these biases emerge in development? At what age do males begin to overperceive female’s interest—19, 17, or perhaps as early as 14? And when do females begin to underperceive male’s interest?

We wanted to find out. Studying topics related to sex among those under 18, however, is—for good reason—highly sensitive and requires great caution. For cultural, practical, and ethical reasons, it is not feasible to ask very young individuals directly about their socio-sexual inference making.

This means there is a lower age limit for what can reasonably be studied. For us, that limit was 16. Using a Norwegian high-school sample of adolescents aged 16 to 19 (N = 1 290), we asked participants to report how often, over the past 12 months, their friendliness had been mistaken for sexual interest—and how often their sexual interest had been mistaken for friendliness.

The results showed that from ages 16 to 19, girls were increasingly—and seemingly linearly—more likely to be overperceived. From age 17 onward, they reported that males exhibited an overperception bias. Boys, on the other hand, were consistently underperceived from age 16, and the frequency of these reports did not change with age. Taken together, these findings suggest that male’s sexual overperception bias strengthens throughout mid-to-late adolescence and may first emerge around age 17. In contrast, female’s sexual underperception bias appears to be activated and relatively stable already by age 16.

In sum, the findings suggest that from age 16 onward, males and females are already heavily engaged in inferring one another’s romantic interest. Like adults, they are frequently exposed both to misinterpreting others and to being misinterpreted themselves—boys more often ending up disappointed and ashamed for overestimating others’ interest, and girls more often confused, embarrassed, and even guilty for feeling they should have noticed that others wanted something more.

Thus, unless someone makes it trendy to disclose romantic interest upfront, the “likes me, likes me not” guessing game will forever remain a classic.

Stavang, Marius, Bendixen, Mons, & Kennair, Leif Edward Ottesen. (2025) Adolescent development of sexual misperception biases: females increasingly overperceived, males consistently underperceived. Evolution and Human Behavior, 46, 106758.

Hot hand thinking in children

– by Andreas Wilke

People often see patterns in completely random data sets, expecting streaks and clumps where none exist. Maybe you’ve recently felt like you’re “on a roll,” or spotted an interesting pattern that later turned out to be non-existent. Here’s the fascinating twist: This tendency isn’t just found in adults. Our new research shows that children as young as three share this propensity—and often even more strongly than adults.

Our recent study published in Evolution and Human Behavior explores how these misperceptions of randomness develop in early childhood. Our findings confirmed something profound about human cognition: Our brains are essentially “wired” to expect streaks and clumps, because, for most of our evolutionary history, resources in nature that we foraged for weren’t random—they were patchy, where a resource encounter often predicted another encounter. If you cast your line and catch a fish, you’re actually pretty smart in thinking more fish may be nearby as well. Similarly, if the first person you encounter in a village speaks your language you will assume others will too. But while we evolved in a world filled full of positively auto-correlated patterns, there are many modern-day settings where events are completely independent leading us to make poor inferences.

Our research reminds us that what sometimes looks like a cognitive fallacy—such as the well-researched hot hand phenomenon—may actually be a design feature, a mental shortcut tuned for survival and resource search in patchy environments. Our brains evolved to expect clumps because, in nature, pure randomness was (and still is) quite rare. This evolved adaptation now still colors how we see the world, from interpreting sequential events to predicting spatial arrangements in various life domains.

So why do we do this? Evolutionary cognitive psychologists argue that this propensity is actually rational from an ecological and evolutionary perspective. For millions of years, humans foraged in environments where resources—plants, animals, water—were clumped together. If you found berries in one spot, chances were good you’d find more nearby. Assuming clumpiness was adaptive for survival, and using any other search strategy in truly random environments would not have lead to lower payoffs. Today, that same mental shortcut misfires in domains like sports, gambling and finance, where outcomes can be truly random.

Until now, research on the hot hand phenomenon focused on adults. Our team wanted to know: When does this bias emerge developmentally? Is it learned through experience, or is it an evolved default present from birth?

To find out, we tested more than 300 children aged 3 to 10 in the U.S. and Germany, using three playful, tablet-based decision-making tasks:

  1. The animal foraging task: Children helped a cartoon rabbit guess whether a carrot was hidden under each spot along a path. The resource sequence path was random, but we measured whether they expected to find clumps of carrots.
  2. The raindrop task: Young participants tapped where they thought raindrops would fall on a basketball court, revealing their mental model of randomness also in two-dimensional space.
  3. The tree task: Children placed apples (which “like to grow close together”) and bird nests (which “like to be spaced out”) on a tree, testing their grasp of positive and negative spatial dependency.

Across all three tasks, children showed a strong bias toward streaks and clumps.

In the animal foraging task, younger children (ages 3–7) consistently predicted streaks, with subjective alternation probabilities well below the objective random benchmark. Older children (ages 8–10) were somewhat better in the task, but often reverted to seeing more clumps in the sequence the longer they played the game.

In the raindrop task, nearly every child produced a pattern that was highly aggregated, as if raindrops fall in clusters. Very few children—often only of older age— created actual random distributions.

In the tree task, kids were better at grouping apples together than spreading bird nests apart, suggesting an earlier readiness for reasoning with positive spatial dependency (clumping) and a delayed grasp of negative dependency (dispersion).

Overall, these assumptions of clumpiness weakened with increased age, but even 10-year-olds still lacked a sound understanding of randomness. Adults, tested in comparison benchmark samples, were more accurate—but also far from perfect.

These findings suggest that hot hand thinking isn’t just a cultural artifact or learned disposition. It appears early in life, likely reflecting an evolved cognitive default shaped by our species’ foraging past. For most of human history, assuming clumps was a smart bet. Today, that same bias can lead us astray.

There are intriguing possibilities for future research. On the one hand, we believe it would be informative to look for ways to identify hot hand thinking even earlier in life—including during infancy, to see what expectations of clumpiness look like, with the most minimal experience and exposure to socio-cultural context. On the other hand, further investigations could look at the effects in later life, say during adolescence, and develop educational trainings to help young people learn what truly random patterns look like.

Understanding this developmental trajectory has practical implications. Teaching statistical literacy early on could help children distinguish real patterns from random noise. This is crucial for science education and decision-making under uncertainty. Since stronger misperceptions of randomness are linked to increased gambling risk, interventions targeting these biases in youth could help reduce problem or pathological gambling later on in life.

So the next time you catch yourself seeing a streak or a pattern in the world out there, remember that it might not be real. It’s a deeply human tendency—one that starts in childhood and tells a story about our evolutionary past.

Wilke, A., DeLaBruere, G., Garcia, Y., Spilman, H., Pedersen, S., Han, B.-H., Barrett, H. C., Todd, P. M., & Wertz, A. E. (2025). Hot hand thinking in children. Evolution and Human Behavior, 46, 106743.