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Starlings form ‘friendships’ to help each other with breeding

Nicola Davis Science correspondent Birds of a feather flock together, so the saying goes. But scientists studying the behaviour of starlings have found their ability to give and take makes their relationships closer to human friendships than previously thought. About 10% of bird species and 5% of mammal species breed “cooperatively”, meaning some individuals refrain from breeding to help others care for their offspring. Some species even help those they are unrelated to. Now researchers studying superb starlings have found the support cuts both ways, with birds that received help in feeding or guarding their chicks returning the favour when the “helper” bird has offspring of its own. Prof Dustin Rubenstein, a co-author of the study from the University of Colombia, said such behaviour was probably necessary for superb starlings as they live in a harsh environment where drought is common and food is limited. “Two birds probably can’t feed their offspring on their own, so they need these helpers to help them,” he said, adding that as each breeding pair produces few offspring, birds must be recruited from outside the family group to help the young survive. “What happens is the non-relatives come into the group, and they breed pretty quickly, usually in the first year, maybe the second year, and then they take some time off and some of the other birds breed – and we never understood why,” said Rubenstein. “But they’re forming these pairwise reciprocal relationships, in the sense that I might help you this year, and then you’ll help me in the future.” The results chime with previous work from Rubenstein and colleagues that found superb starlings living in larger groups have a greater chance of survival and of producing offspring, with the new work suggesting the give-and-take approach helps to stabilise these groups. © 2025 Guardian News & Media Limited

Related chapters from BN: Chapter 6: Evolution of the Brain and Behavior; Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases
Related chapters from MM:Chapter 8: Hormones and Sex
Link ID: 29785 - Posted: 05.14.2025

Frog ribbits erupt via an extravagant variety of vocal sacs

By Susan Milius Here’s a great case of real life turning out to be stranger than fiction. From baby’s first storybook to sly adult graphic novels, the story we’re told is the same: Male frogs croak with the bottom of their mouths ballooning out in one fat, rounded bubble. Yet “that’s actually only half the species of frogs,” says herpetologist Agustín Elías-Costa of the Bernardino Rivadavia Natural Science Museum in Buenos Aires. The diversity of body parts for ribbitting is astounding. Some males serenade with a pair of separate puff-out disks like padded headphones that slipped down the frog’s neck, throbbing in brilliant blue. Some have sacs that look like balloon Mickey Mouse ears in khaki. Others ribbit with a single upright like a fat horn stub on some inflatable swimming pool toy rhino. All together, 20 basic forms for vocal sacs have evolved among frogs and toads, Elías-Costa and herpetologist Julián Faivovich report in March in the Bulletin of the American Museum of Natural History. Still, about 18 percent of the 4,358 species examined didn’t have vocal sacs at all. The team studied 777 specimens over 10 years of visiting museums around the world, including the Smithsonian’s National Museum of Natural History in Washington, D.C. “Libraries of nature,” Faivovich calls them. Just drawing a picture of something doesn’t authenticate details the way a preserved specimen does. These collections for biodiversity studies are “what makes them a science,” he says. The survey showed that vocal sacs disappeared between 146 and 196 times across the very twiggy evolutionary branchings of the frog and toad family tree. That’s “an astounding number considering their biological importance,” Elías-Costa says. Even without sacs, the animals still emit sounds because, like human speech, frog and toad ribbits originate from the larynx. Vocal sacs amplify the sound and could convey nuances of male quality and sexiness, but can also tip off eavesdropping predators. Females in a few species vocalize too, but it’s mostly a male endeavor. © Society for Science & the Public 2000–2025.

Related chapters from BN: Chapter 9: Hearing, Balance, Taste, and Smell; Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases
Related chapters from MM:Chapter 6: Hearing, Balance, Taste, and Smell; Chapter 8: Hormones and Sex
Link ID: 29774 - Posted: 05.07.2025

What birds can teach us about the ‘biological truth’ of sex

By Nicole M. Baran One of the biggest misconceptions among students in introductory biology courses is that our characteristics are determined at conception by our genes. They believe—incorrectly—that our traits are “immutable.” The much more beautiful, complicated reality is that we are in fact a product of our genes, our environment and their interaction as we grow and change throughout our lives. Nowhere is this truer than in the developmental process of sexual differentiation. Early in development when we are still in the womb, very little about us is “determined.” Indeed, the structures that become our reproductive system start out as multi-potential, capable of taking on many possible forms. A neutral structure called the germinal ridge, for example, can develop into ovaries or testes—the structures that produce reproductive cells and sex hormones—or sometimes into something in between, depending on the molecular signals it receives. Our genes influence this process, of course. But so do interactions among cells, molecules in our body, including hormones, and influences from the outside world. All of these can nudge development in one direction or another. Understanding the well-studied science underlying this process is especially important now, given widespread misinformation about—and the politicization of—sex and gender. I am a neuroendocrinologist, which means that I study and teach about hormones and the brain. In my neuroendocrinology classroom, students learn about the complex, messy process of sexual differentiation in both humans and in birds. Because sexual differentiation in birds is both similar to and subtly different from that in humans, studying how it unfolds in eggs can encourage students to look deeper at how this process works and to question their assumptions. So how does sexual differentiation work in birds? Like us, our feathered friends have sex chromosomes. But their sex chromosomes evolved independently of the X and Y chromosomes of mammals. In birds, a gene called DMRT1 initiates sexual differentiation. (DMRT1 is also important in sexual differentiation in mammals and many other vertebrate animals.) Males inherit two copies of DMRT1 and females inherit only one copy. Reduced dosage of the gene in females leads to the production of the sex hormone estradiol, a potent estrogen, in the developing embryo. © 2025 Simons Foundation

Related chapters from BN: Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases; Chapter 6: Evolution of the Brain and Behavior
Related chapters from MM:Chapter 8: Hormones and Sex
Link ID: 29759 - Posted: 04.26.2025

Does testosterone make men?

is a psychologist, writer and professor in the history and philosophy of science programme at the University of Melbourne. She is the author of Delusions of Gender: How Our Minds, Society, and Neurosexism Create Difference (2010), Testosterone Rex: Myths of Sex, Science, and Society (2017) and Patriarchy Inc.: What We Get Wrong About Gender Equality – and Why Men Still Win at Work (2025). She lives in Melbourne, Australia. Carole Hooven is a human evolutionary biologist with a focus on behavioural endocrinology. She is a nonresident senior fellow at the American Enterprise Institute, an associate in Harvard’s Department of Psychology, and the author of T: The Story of Testosterone, the Hormone That Dominates and Divides Us (2021). She lives in Cambridge, Massachusetts. Does biology determine destiny, or is society the dominant cause of masculine and feminine traits? In this spirited exchange, the psychologist Cordelia Fine and the evolutionary biologist Carole Hooven unpack the complex relationship between testosterone and human behaviour. Fine emphasises variability, flexibility and context – seeing gender as shaped by social forces as much as it is by hormones. By contrast, Hooven stresses consistent patterns; while acknowledging the influence of culture and the differences between individuals, she maintains that biology explains why certain sex-linked behaviours persist across cultures. © Aeon Media Group Ltd. 2012-2025.

Mating and Monogamy: The Tricky Sex Lives of Birds

By Nathan H. Lents For generations, anthropologists have argued whether humans are evolved for monogamy or some other mating system, such as polygyny, polyandry, or promiscuity. But any exploration of monogamy must begin with a bifurcation of the concept into two completely different phenomena: social monogamy and sexual monogamy. WHAT I LEFT OUT is a recurring feature in which book authors are invited to share anecdotes and narratives that, for whatever reason, did not make it into their final manuscripts. In this installment, author Nathan H. Lents, professor of biology at John Jay College, shares a story that didn’t make it into his recent book “The Sexual Evolution: How 500 Million Years of Sex, Gender, and Mating Shape Modern Relationships” (Mariner Books). Sexual monogamy is just what it sounds like: The restriction of sexual intercourse to within a bonded pair. Social monogamy, also known as economic monogamy, describes the bonding itself, a strong, neurohormone-driven attachment between two adults that facilitates food and territory sharing, to the exclusion of others, for at least one breeding season, and generally purposed towards raising offspring. Because these two aspects of monogamy are so often enjoined among humans, they are considered two sides of the same coin. But, as it turns out, they are entirely separable among animals. In fact, social monogamy is extremely common in birds and somewhat common in mammals, while sexual monogamy is vanishingly rare among any species. Because of the unique way their embryos develop — externally but with constant warmth required — birds are the real stars of monogamy and have thus borne the brunt of its misconceptions. The marriage (if you’ll pardon the pun) of two very different behaviors into one concept is — and always was — unsupported by evidence from the natural world. Monogamy, as it is commonly understood, was the invention of anthropomorphic bias. Naturalists in the 19th and 20th centuries documented how pairs of various bird species dutifully toiled together building a nest, protecting the eggs, mutually feeding each other and their offspring, before eventually flying off into the sunset together. These prim and proper Victorians didn’t have to squint very hard to see a perfect model in nature of what they valued most in human society — lifelong and sexually exclusive marriage.

Why women’s brains are more resilient: it could be their ‘silent’ X chromosome

By Katherine Bourzac Women tend to live longer than men and are often more resilient to cognitive decline as they age. Now researchers might have uncovered a source for this resilience: the second X chromosome in female cells that was previously considered ‘silent’. In work published today in the journal Science Advances1, a team reports that, at least in female mice, ageing activates expression of genes on what is usually the ‘silent’, or inactivated, X chromosome in cells in the hippocampus, a brain region crucial to learning and memory. And when the researchers gave mature mice of both sexes a type of gene therapy to boost expression of one of those genes, it improved their cognition, as measured by how well they explored a maze. Assuming these results can be confirmed in humans, the team suggests it could mean that women’s brains are being protected by their second X chromosome as they age — and that the finding could translate into future therapies boosting cognition for everyone. “The X chromosome is powerful,” says Rachel Buckley, a neurologist who studies sex differences in Alzheimer’s disease at Massachusetts General Hospital in Charlestown, and who was not involved in the research. This kind of work, she says, is helping researchers to understand “where female resilience lies and how to harness it”. (This article uses ‘women’ and ‘female’ to describe people with two X chromosomes and no Y chromosome, reflecting the language of the study. Nature recognizes that not all people who identify as women have this chromosomal make-up.) Double dose Female cells typically have two X chromosomes, one from each parent; male cells usually have one X and one Y. Early in development, one of the two X chromosomes in female cells is inactivated — coated in various proteins and RNA molecules that prevent its genes from being expressed. Which one is ‘silenced’ — meaning which parent it comes from — is random, and the tissues in the body are a mosaic of both types. © 2025 Springer Nature Limited

Related chapters from BN: Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases; Chapter 15: Emotions, Aggression, and Stress
Related chapters from MM:Chapter 8: Hormones and Sex; Chapter 11: Emotions, Aggression, and Stress
Link ID: 29698 - Posted: 03.08.2025

This Backyard Bird Has a Lot to Teach Us about Sex Variability

By Donna L. Maney It’s springtime in your backyard. You watch a pair of little brown songbirds flit about, their white throats flashing in the sun. One of the birds has striking black and white stripes on its crown and occasionally belts out its song, “Old Sam Peabody, Peabody, Peabody.” Its partner is more drab, with tan and gray stripes on its head and brown streaks through its white throat. Knowing the conventional wisdom about songbirds—that the males are flashy show-offs and the females more camouflaged and quiet—you decide to name the singer with bright plumage Romeo and the subtler one Juliet. But later that day you notice Juliet teed up on the fence, belting out a song. Juliet’s song is even louder and showier than Romeo’s. You wonder, Do female birds sing? Then you see Romeo bringing a twig to the pair’s nest, hidden under a shrub. Your field guide says that in this species the female builds the nest by herself. What is going on? Turns out, when you named Romeo and Juliet, you made the same mistake 19th-century artist and naturalist John Audubon did when, in his watercolor of this species, he labeled the bright member of the pair “male” and the drab one “female.” Romeo might look male, even to a bird expert such as Audubon, but will build a nest and lay eggs in it. Juliet, who might look female, has testes and will defend the pair’s territory by singing both alone and alongside Romeo, who also sings. Juliet and Romeo are White-throated Sparrows (Zonotrichia albicollis). At first glance, members of this species of songbird might look rather ordinary. For example, like many other songbirds, one member of each breeding pair of these sparrows has more striking plumage—that is, its appearance is what we would traditionally consider malelike for songbirds. The other bird in the pair is more femalelike, with drabber plumage. © 2024 SCIENTIFIC AMERICAN

Birds of Paradise Glow on Mating Parade

By Jason Bittel Elaborate poses, tufts of feathers, flamboyant shuffles along an immaculate forest floor — male birds-of-paradise have many ways to woo a potential mate. But now, by examining prepared specimens at the American Museum of Natural History in New York, scientists have discovered what could be yet another tool in the kit of the tropical birds — a visual effect known as photoluminescence. Sometimes called biofluorescence in living things, this phenomenon occurs when an object absorbs high-energy wavelengths of light and re-emits them as lower energy wavelengths. Biofluorescence has already been found in various species of fishes, amphibians and even mammals, from bats to wombats. Interestingly, birds remain woefully understudied when it comes to the optical extras. Until now, no one had looked for the glowing property in birds-of-paradise, which are native to Australia, Indonesia and New Guinea and are famous for their elaborate mating displays. In a study published on Tuesday in the journal Royal Society Open Science, researchers examined prepared specimens housed at the American Museum of Natural History and found evidence of biofluorescence in 37 of 45 birds-of-paradise species. “What they’re doing is taking this UV color, which they can’t see, and re-emitting it at a wavelength that is actually visible to their eyes,” said Rene Martin, the lead author of the study and a biologist at the University of Nebraska-Lincoln. “In their case, it’s kind of a bright green and green-yellow color.” In short, biofluorescence supercharges a bright color to make it even brighter. © 2025 The New York Times Company

Revisiting sex and gender in the brain

By Marija Kundakovic The role of sex and gender in the brain is a popular but controversial research topic. Neuroscience has a reputation for being male-centric and focused on studying male brains, although researchers have recently embraced the idea that it is critical to study female brains as well. Generally speaking, human female and male brains are morphologically similar, but that does not suggest they don’t differ in their activity and function, or in their underlying molecular and cellular mechanisms. In fact, sex and gender bias in neuropsychiatric conditions is the rule rather than the exception. Men are three to five times as likely as women to have autism or attention-deficit/hyperactivity disorder, for example, and women are twice as likely as men to have anxiety or depression disorders. Understanding the biological factors and mechanisms that underlie gender- and sex-related bias in brain function and psychiatric conditions is essential to improve our fundamental knowledge of the brain and to open a path to develop novel, sex-informed treatments. But simply including females in research studies is insufficient to resolve the role of sex and gender in neuroscience. “Sex” and “gender” are both complex and evolving concepts, extending beyond a simple binary. In practice, people are assigned female or male at birth based on external genitalia, although up to 2 percent do not belong to either category because of differences in sex development. Though gender has traditionally been co-assigned with sex—females/women and males/men—the binary nature of sex does not suffice to account for today’s expanding gender landscape. Gender exists on a spectrum, including nonbinary, gender-fluid and agender people. In transgender people, gender identity differs from gender or sex assigned at birth. Some researchers would say that this complexity cannot (and perhaps should not) be tackled by science, and that we should stick to scientifically discernible female-male comparisons, particularly in animal research. But science should not exist in a vacuum; when detached from society, it does not serve its purpose. Indeed, in the case of gender, biology can be falsely used to fuel discriminatory laws and practices against gender-diverse and gender-non-conforming people, supposedly based on a scientific understanding of “biological sex.” © 2025 Simons Foundation

Related chapters from BN: Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases
Related chapters from MM:Chapter 8: Hormones and Sex
Link ID: 29651 - Posted: 02.01.2025

Brain gene expression syncs between bonded prairie voles

By Shaena Montanari Just as romantic partners exhibit more similar brain waves than do strangers when, say, drawing on an Etch A Sketch toy together, animal pairs also show neural synchrony during social interactions and cooperation tasks. “Neural synchrony is something that happens in these minute-to-minute engagements that you have with another individual,” says Zoe Donaldson, associate professor of behavioral neuroscience at the University of Colorado Boulder. But over time, too, pairs in a relationship learn to infer what their partner is going to do, she adds. In prairie voles, at least, that learning process may unfold at the molecular level in the form of “transcriptional synchrony,” according to a preprint Donaldson and her colleagues posted on bioRxiv in November. Prairie voles are socially monogamous, and after two of them bond, gene-expression patterns in their nucleus accumbens—a forebrain region linked to reward and social interaction—start to align. It remains unclear whether this transcriptional synchrony causes pair bonding or only correlates with it, she adds, but in the meantime, it offers researchers a new place to hunt for the basis of these strong social ties. This new study “pushes the limits of what’s possible” technically, says Robert Froemke, professor in New York University’s Neuroscience Institute and otolaryngology department, who was not involved in the study. Though the existence of neural synchrony logically suggests that there may also be shared patterns of gene expression, “it’s still remarkable to actually have it documented,” he says. The new preprint offers the first evidence of transcriptional synchrony in prairie voles, Donaldson says, but a 2020 study revealed that fighting pairs of Betta splendens fish show a strong correlation of gene expression after 60 minutes of fighting, and only a weak correlation after 20 minutes. © 2025 Simons Foundation

Related chapters from BN: Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases; Chapter 5: Hormones and the Brain
Related chapters from MM:Chapter 8: Hormones and Sex; Chapter 8: Hormones and Sex
Link ID: 29630 - Posted: 01.15.2025

She ain’t scary, she’s my mother

By Tim Vernimmen Few people are fond of earwigs, with their menacing abdominal pincers — whether they’re skittering across your floor, getting comfy in the folds of your camping tent or minding their own business. Scientists, too, have given them short shrift, compared with the seemingly endless attention they have lavished on social insects like ants and bees. Yet there are a handful of exceptions. Some researchers have made conscious career decisions to dig into the hidden, underground world where earwigs reside, and have found the creatures to be surprisingly interesting and social, if still not exactly endearing. Work in the 1990s and early 2000s focused on earwig courtship. These often-intricate performances of attraction and repulsion — in which pincers and antennae play prominent roles — can last hours, and the mating itself as long as 20 hours, at least in one Papua New Guinea species, Tagalina papua. The females usually decide when they’ve had enough, though males of some species use their pincers to restrain the object of their desire. Males of the bone-house earwig Marava arachidis (often found in bone meal plants and slaughterhouses) are particularly coercive, says entomologist Yoshitaka Kamimura of Keio University in Japan, who has studied earwig mating for 25 years. “They bite the female’s antennae and use a little hook on their genitalia to lock them inside her reproductive tract.” Size matters

Related chapters from BN: Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases
Related chapters from MM:Chapter 8: Hormones and Sex
Link ID: 29559 - Posted: 11.16.2024

Did the human kiss begin as an ape grooming ritual?

By Phie Jacobs Whether it’s two newlyweds going in for a smooch after saying “I do” or a parent soothing their child’s scraped knee, kissing is one of humanity’s most recognizable symbols of affection. Clay tablets from ancient Mesopotamia dating to 2500 B.C.E. provide the earliest archaeological evidence of romantic kissing. But the behavior may be older than civilization itself, with some studies suggesting Neanderthals swapped spit with modern humans—and shared each other’s oral microbes—more than 100,000 years ago. Some researchers have suggested kissing evolved from behaviors such as sniffing, nursing babies, or even parents passing chewed-up food to their offspring. But in an article published this month in Evolutionary Anthropology, evolutionary psychologist Adriano Lameira of the University of Warwick offers another hypothesis. Drawing on his knowledge of great ape behavior, Lameira suggests kissing got its start as a fur grooming ritual still observed in modern-day chimpanzees and other great apes. Science sat down with Lameira to learn more about his work. This interview has been edited for length and clarity. Q: What made you want to study kissing? A: It’s a behavior that is charged with so much meaning and symbolism, perhaps the most iconic way of how we show affection on an individual and societal level. I was surprised to find that we know so little about its evolution and nature. In our lab, we’re mostly intrigued by the evolution of language, dance, and imagination. But in the largest sense we’re interested in behaviors and rituals that are evolutionary heirlooms from our apelike ancestors—things our ancestors did that set us on course towards who we are today. Q: Do other animals kiss, or is the behavior unique to humans? © 2024 American Association for the Advancement of Science.

Are you my baby? The clever ways that brood parasites trick other birds

By Sofia Quaglia Parenting can be lots of work for a bird: all that flying back and forth transporting grubs and insects to a nest of demanding young. But some birds manage to forgo caring for their chicks — while still ensuring they’re well looked after. These birds lay their eggs in the nests of other birds that unknowingly adopt the hatchlings, nourishing and protecting them as their own. Only about 1 percent of all bird species resort to this sneaky family planning method, called obligate brood parasitism, but it has evolved at least seven separate times in the history of birds and is a way of life for at least 100 species. Since some brood parasites rely on several different bird species as foster parents, more than a sixth of all species in the avian world care for chicks that aren’t their own at some point. Throughout the millennia, these trespassers have evolved ingenious ways to fool the hosts, and the hosts have developed equally clever ways to protect themselves and their own. At each stage of the nesting cycle, it’s a game of subterfuge that plays out in color, sound and behavior. “There’s always something new — it’s like, ‘Oh, man, this group of birds went down a slightly different pathway,’” says behavioral ecologist Bruce Lyon of the University of California, Santa Cruz, who studies the black-headed duck (Heteronetta atricapilla), the sole obligate parasitic duck species. While many mysteries remain, new research is constantly unearthing just how intense this evolutionary tug-of-war can get.

Pregnancy overhauls the brain. Here’s what that looks like

By Laura Sanders Pregnancy overhauls a woman’s body. The brain is no exception. A detailed study of a woman’s brain before, during and after pregnancy revealed sweeping neural changes, some of which stuck around months after her baby was born. The dataset, published September 16 in Nature Neuroscience, is the first comprehensive view of the neural changes that accompany gestation — a sort of “what to expect when you’re expecting” for the brain. “The results of this case study are astonishing,” says neuroscientist Clare McCormack of New York University Langone Health. “Here we see, for the first time in humans, the extent of brain changes that are under way throughout pregnancy.” This research joins a small number of other studies aimed at understanding the female brain at various stages of life (SN: 9/29/22). Collectively, the work suggests that the process of becoming a mother, called matrescence, is another stage of development, like the brain overhaul that happens in adolescence (SN: 2/27/23). Earlier experiments mostly compared brains of women before and after their pregnancies and inferred what happens in between (SN: 12/19/16). “There was a missing piece,” McCormack says. “The nine months of pregnancy was a black box, and we could only guess what that trajectory looks like.” With four MRI scans before pregnancy, 15 scans during pregnancy and seven scans in the two years after the baby was born, the new study follows the entire arc for one mother. © Society for Science & the Public 2000–2024.

How pregnancy transforms the brain to prepare it for parenthood

By Liam Drew In November 2008, neuroscientist Susana Carmona — then a postdoc studying attention deficit hyperactivity disorder — was driving two colleagues to a party when one of them revealed that she was thinking about having a child. The trio became so engulfed in conversation about how pregnancy might change her brain that they diverted from the party and headed to their laboratory to search the literature. They found numerous studies in rodents, but in humans, “there was basically nothing at all”, says Carmona. Shocked by this gap in research, Carmona and her colleagues convinced their mentor at the Autonomous University of Barcelona, Spain, Oscar Vilarroya, to let them run a study using magnetic resonance imaging (MRI) to measure the neuroanatomy of women before they became pregnant, and then again after they gave birth. Squeezed in alongside their main projects, the investigation took eight years and included dozens of participants. The results, published in 2016, were revelatory1. Two to three months after giving birth, multiple regions of the cerebral cortex were, on average, 2% smaller than before conception. And most of them remained smaller two years later. Although shrinkage might evoke the idea of a deficit, the team showed that the degree of cortical reduction predicted the strength of a mother’s attachment to her infant, and proposed that pregnancy prepares the brain for parenthood. Today, Carmona, now at the Gregorio Marañón Health Research Institute in Madrid, is one of several scientists uncovering how pregnancy and parenthood transform the brain. Elseline Hoekzema, one of Carmona’s passengers that evening in 2008, is another. In 2022, Hoekzema, who is now at the Amsterdam University Medical Centre in the Netherlands, confirmed that the cortical regions that shrink during pregnancy also function differently for at least a year after giving birth2. These studies and others, say researchers, highlight a transformational life event that has long been neglected by neuroscience — one that around 140 million women experience annually.

Related chapters from BN: Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases; Chapter 17: Learning and Memory
Related chapters from MM:Chapter 8: Hormones and Sex; Chapter 13: Memory and Learning
Link ID: 29418 - Posted: 08.02.2024

These brain cells help days-old mice to bond with mum

By Miryam Naddaf Researchers have identified neurons in the brains of baby mice that enable them to form a unique, strong bond with their mother in the first few days of life. Stimulating these neurons in mouse pups that had been separated from their mother could mimic the soothing effect of their mother’s presence, and reduced behaviours associated with stress. The findings, published today in Science1, offer fresh clues about the formation of the mother–infant bond in mammals, and could help researchers to better understand how brain development influences behaviour. “We know very little about how the brains of infants make sense of their social world,” says study co-author Marcelo Dietrich, a neurobiologist at Yale University in New Haven, Connecticut. “When I started my lab ten years ago, and I wanted to study this kind of stuff, people said it was delusional. It will fail. It’s too difficult.” Now, “we show that it’s possible: one can do rigorous science and try to understand these mechanisms that are potentially very important for development and health”. “I see these neurons as the ‘I feel good with mommy’ neurons,” says Catharine Dulac, a neuroscientist at the University of Harvard in Cambridge, Massachusetts. “The features that [they] discovered provide some framework to think about humans.” Bonding in the brain Dietrich and his team studied nursing mouse pups that were between 16 and 18 days old. They used live imaging techniques to record activity in the zona incerta (ZI), a thin layer of grey matter located below the thalamus, while the animals interacted with their mother. © 2024 Springer Nature Limited

Related chapters from BN: Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases
Related chapters from MM:Chapter 8: Hormones and Sex
Link ID: 29409 - Posted: 07.27.2024

Brain imaging study in children shows sex and gender operate in different networks of the brain

By Phie Jacobs Is there really such a thing as a “male” or “female” brain? Sex certainly seems to affect a person’s risk of developing various psychiatric and other brain-related conditions—but scientists aren’t entirely sure why. Attention-deficit/hyperactivity disorder for example, is more commonly diagnosed in individuals who were assigned male at birth (AMAB), whereas those assigned female at birth (AFAB) are more likely to exhibit symptoms of anxiety. It’s unclear, however, whether these differences are actually driven by sex, or have more to do with how people are perceived and treated based on their sex or gender. Now, new research suggests sex and gender are associated with distinct brain networks. Published today in Science Advances, the findings draw on brain imaging data from nearly 5000 children to reveal that gender and sex aren’t just distinct from one another in society—they also play unique roles in biology. In science, the term “biological sex” encompasses a variety of genetic, hormonal, and anatomical characteristics. People are typically assigned “male” or “female” as their sex at birth, although the medical establishment in recent years has begun to acknowledge that sex doesn’t always fall neatly into binary categories. Indeed, about 0.05% of children born in the United States are assigned intersex at birth. Gender, by contrast, has more to do with a person’s attitudes, feelings, and behavior—and may not always align with the sex they were assigned at birth. These nuances often go unrecognized in neuroscience, says Sheila Shanmugan, a reproductive psychiatrist at the University of Pennsylvania who wasn’t involved in the new study. Sex and gender-based differences in the brain “have historically been understudied,” she explains, “and terms describing each are often conflated.” © 2024 American Association for the Advancement of Science.

Sensory secrets of penis and clitoris unlocked after more than 150 years

By Sara Reardon Specific nerve cells on the penis and clitoris detect vibrations and then become activated, causing sexual behaviours such as erections, a study in mice has revealed1. The findings could lead to new treatments for conditions such as erectile dysfunction, or for restoring sexual function in people with lower-body paralysis. Krause corpuscles — nerve endings in tightly wrapped balls located just under the skin — were first discovered in human genitals more than 150 years ago. The structures are similar to touch-activated corpuscles found on people’s fingers and hands, which respond to vibrations as the skin moves across a textured surface. But there is little research into how the genital corpuscles work and how they are involved in sex, probably because the topic is sometimes considered taboo. “It’s been hard to get people to work on this because some people have a hard time talking about it,” says David Ginty, a sensory neurobiologist at Harvard Medical School in Boston, Massachusetts, who led the team that conducted the latest research. “But I don’t, because the biology is so interesting.” Ginty and other sensory biologists have long wanted to study these mysterious neuron balls. But activating and tracking specific neurons was nearly impossible until advanced molecular techniques emerged in the past 20 years. In a 19 June paper in Nature1, Ginty and his collaborators activated the Krause corpuscles in both male and female mice using various mechanical and electrical stimuli. The neurons fired in response to low-frequency vibrations in the range of 40–80 hertz. Ginty notes that these frequencies are generally used in many sex toys; humans, it seems, realized that this was the best way to stimulate Krause corpuscles before any official experiments were published. © 2024 Springer Nature Limited

Related chapters from BN: Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases; Chapter 8: General Principles of Sensory Processing, Touch, and Pain
Related chapters from MM:Chapter 8: Hormones and Sex; Chapter 5: The Sensorimotor System
Link ID: 29365 - Posted: 06.24.2024

More playful young male dolphins father more offspring

By Virginia Morell Leaping over waves or body surfing side by side, dolphins are a fun-loving bunch. But their frolicking—and that of species from hyenas to humans—has long baffled evolutionary biologists. Why expend so much energy on play? A new study offers an intriguing explanation: Juvenile male dolphins use play to acquire the skills required for fathering calves, researchers report today in the Proceedings of the National Academy of Sciences. Most significantly, the scientists found the most playful males go on to have more calves as adults. The study is likely to spur further research into play behavior in additional species, other scientists say. “It’s exciting research, and it solves an evolutionary puzzle,” says Jennifer Smith, a behavioral ecologist at the University of Wisconsin–Eau Claire. “This is the first study to link play behavior in the wild to reproductive success.” Since 1982, scientists have observed some 200 male Indo-Pacific bottlenose dolphins (Tursiops aduncus) in the exceptionally clear waters of Shark Bay in Australia. About 20 years ago, the researchers noticed that young males, 4 to 12 years old, often played together as if they were herding a fertile female, flanking her on either side, while swimming in sync with each other and making popping vocalizations. This kind of “synchronicity is crucial for male reproduction,” says Kathryn Holmes, a behavioral biologist with the Shark Bay Dolphin Research project and lead author of the new study. The young dolphins’ behaviors were strikingly similar to those of the adults. “We wondered if this was ‘play practice’ for the adult behaviors,” Holmes says. So she and her colleagues closely tracked 28 juvenile males for 4 to 5 months over several years, recording their interactions and play behaviors. When socializing, the males “played almost continuously,” Holmes says. “They seemed to never tire of their games.” © 2024 American Association for the Advancement of Science.

'Chimney caps, vent pipes, gutters': Why some woodpeckers are major metal heads

Sacha Pfeiffer A few weeks ago, at about 6:45 in the morning, I was at home, waiting to talk live on the air with Morning Edition host Michel Martin about a story I'd done, when I suddenly heard a loud metallic hammering. It sounded like a machine was vibrating my house. It happened again about 15 seconds later. And again after that. This rhythmic clatter seemed to be coming from my basement utility closet. Was my furnace breaking? Or my water heater? I worried that it might happen while I was on the air. Luckily, the noise stopped while I spoke with Michel, but restarted later. This time I heard another sound, a warbling or trilling, possibly inside my chimney. Was there an animal in there? I ran outside, looked up at my roof — and saw a woodpecker drilling away at my metal chimney cap. I've seen and heard plenty of woodpeckers hammer on trees. But never on metal. So to find out why the bird was doing this, I called an expert: Kevin McGowan, an ornithologist at the Cornell Lab of Ornithology who recently created a course called "The Wonderful World of Woodpeckers." McGowan said woodpeckers batter wood to find food, make a home, mark territory and attract a mate. But when they bash away at metal, "what the birds are trying to do is make as big a noise as possible," he said, "and a number of these guys have found that — you know what? If you hammer on metal, it's really loud!" Woodpeckers primarily do this during the springtime breeding season, and their metallic racket has two purposes, "basically summarized as: All other guys stay away, all the girls come to me," McGowan said. "And the bigger the noise, the better." © 2024 npr

Related chapters from BN: Chapter 12: Sex: Evolutionary, Hormonal, and Neural Bases; Chapter 19: Language and Lateralization
Related chapters from MM:Chapter 8: Hormones and Sex; Chapter 15: Language and Lateralization
Link ID: 29333 - Posted: 06.02.2024

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