Scientists Recreated Chirps of Jurassic Insects, Simulating a 165 Million-yo Soundscape (Listen)

– credit, Jun-Jie Gu et al., PNAS 2026

It wasn’t just the roars of the dinosaurs that made up the soundscape of the animal world during the Jurassic period.

Crickets and grasshoppers communicated through a variety of songs and high-pitched sounds, some of which you can now listen to thanks to Thorin Jonsson from the Institute of Biology at the University of Graz.

Together with his colleagues from the universities of Lincoln, Bristol (UK), Beijing (China), and Tempe (USA) their findings on what are so far the oldest traces of sound on Earth have just been published in the journal PNAS.

Insects from the order Orthoptera, such as crickets and grasshoppers, rub wing structures against one another or against their legs to produce sounds called “stridulations.” Pitch and rhythm depend on the number and spacing of the teeth on the wing’s ridge, as well as the shape and movement of the wings.

Though vocal cords and other biological acoustic organs can’t be fossilized along with the sounds they made, the imprints left by these wings confer very precise information on the animal’s stridulations.

Jonsson’s Chinese research partners have discovered extremely well-preserved fossils of 9 different grasshopper species that lived at the same time in the same region, namely during the Middle Jurassic period in what is now Inner Mongolia.

The sound-producing structures are so clearly visible on these fossils that the biologists were able to reconstruct the pitches and musical units of the mating calls through various analyses, simulations, and AI-assisted evaluations that even produced the specific number of hertz each insect would sound off at.

“Our findings reveal a wide variety of call frequencies. Several species produced pure, low-pitched sounds like modern crickets, whilst others produced higher frequencies, similar to our native leafhoppers,” reports Jonsson.

The study isn’t just the first to do this with insects. It’s the oldest evidence of sound ever reproduced by anyone. Think of it like the famous Epitaph of Seikilos. This Greek funerary song was inscribed on a gravestone, and is able to be read by musicians several thousand years after it was last played.

Similarly, the physical features on the grasshoppers’ wings act like musical notation, and though scientists can’t reproduce them on a lyre like the Epitaph of Seikilos, AI can simulate them on a computer sound board.

One species among the 9 surprised the researchers. A relative of the katydid called Sigmaboilus peregrinus communicated in the ultrasonic range between 20 and 22 kilohertz—a frequency that’s just above the human range of hearing.

For all the delicious proof of concept novelty the study provided, this discovery carries implications for the evolutionary biology of Orthoptera.

It was previously theorized that stridulatory insects whose stridulations reach into ultrasonic frequencies were pressured to do so by the incredibly precise hearing of bats. However, S. peregrinus lived millions of years before the first known bat existed.

The team took the liberty afforded by their discovery to hypothesize other reasons why an animal would have to vocalize at such high frequencies. While not a bat, it could have been an example of the insect attempting to avoid detection by other predators. Alternatively, it could be a mating strategy by males to allow their calls to rise above the din of the Jurassic jungle night.“This allowed us to demonstrate that the world during the Jurassic Period was acoustically far richer and more diverse than previously thought,” the biologist summarizes. Scientists Recreated Chirps of Jurassic Insects, Simulating a 165 Million-yo Soundscape (Listen)
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Survey Finds Blackbirds to Have the Most Beautiful Songs in the Avian World–Science Explains Why

– SWNS

The next time you hear a blackbird singing in the dead of night, know that you’re listening to the most pleasant song in the world.

What the bird lacks in dressage it makes up for in repertoire, a new survey and study from the University of Tübingen found in which researchers set out to discover the key ingredients that make birdsong pleasant.

The blackbird topped the ‘pleasantness’ table with an average score of 4.52 out of 5, beating the willow warbler to first position (4.45) . The blackcap filled out the top 3.

“You don’t have to be a ‘bird person’ to find bird sounds beautiful,” said study author Dr. Nadine Kalb from Tübingen U. “Being able to recognize birds by their appearance or song did not affect how people rated calls.”

By asking people to listen to birdsongs and rate them for pleasantness, then cross-referencing the results with information about the calls’ acoustic characteristics, Kalb and co-authors identified key aspects that make some birdsongs seem more pleasant than others.

Participants rated the perceived pleasantness of 123 different bird songs on a scale from 1 (not very pleasant) to 5 (very pleasant). Calls which are varied, higher-pitched, and not too loud are considered most pleasant.

The research team suspected that some acoustic characteristics, such as a high amplitude—perceived as a loud noise—would be associated with a lower pleasantness rating.

But they also suspected some personal characteristics, such as individuals’ knowledge about birds, would influence pleasantness ratings, and so participants were also asked questions which measured their birding skills and their perception of birds.

“I’m very interested in human-bird relationships,” said senior study author Dr. Christoph Randler, also from the University of Tübingen.

“Bird sounds are often considered one of the most enjoyable aspects of spending time in nature, and previous research has shown that they can contribute to psychological restoration and well-being. However, not all bird sounds are perceived equally positively.”

For example, the barn owl finished rock bottom with an average pleasantness score of just 1.32.

A narrower bandwidth, which captures the range of frequencies a song used, and greater complexity, the number and variety of elements in the song, were perceived as more pleasant, as were birdsongs at a higher frequency or with a relatively low amplitude. The songs that scored highest also avoided a key frequency range where human hearing is highly sensitive.

“We might be wired to prefer more variable sounds with moderate amplitudes and frequencies because they signal a safe, healthy, and restorative environment where we can relax,” said Dr. Kalb.

To follow up the research, they want to carry out larger studies with broader samples including more men, different cultures, and more experienced birdwatchers.

“I would love to investigate how bird sounds influence people in real-world environments,” Dr. Randler said. “That would help us better understand the role that healthy ecosystems play in supporting both biodiversity and human well-being.”

Top 20 Most Pleasant (Old World) Bird Songs
  • 1. Common Blackbird (4.52 average pleasantness score)
  • 2. Willow Warbler (4.45)
  • 3. Blackcap (4.43)
  • 4. Mistle Thrush (4.33)
  • 5. Garden Warbler (4.30)
  • 6. Dunnock (4.30)
  • 7. Chaffinch (4.29)
  • 8. Common Nightingale (4.26)
  • 9. Common Linnet (4.26)
  • 10. European Goldfinch (4.26)
  • 11. European Pied Flycatcher (4.25)
  • 12. Eurasian Wren (4.24)
  • 13. Skylark (4.23)
  • 14. Eurasian Golden Oriole (4.17)
  • 15. Common Cuckoo (4.13)
  • 16. Tree Pipit (4.08)
  • 17. Common Redstart (4.08)
  • 18. European Greenfinch (4.08)
  • 19. Eurasian Treecreeper (4.05)
  • 20. European Robin (4.04) 
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When Zoo Elephants Are Rewilded in Africa, Here’s How Good Their Coping Skills Are

Rewilded elephants on Khamab Kalahari Reserve – Elephant Reintegration Trust of South Africa / SWNS

New research shows that elephants develop successful coping mechanisms when returning to the wild from human captivity.

In fact, the team found that “rewilded” elephants can fit quite well within wildlife systems and readapt—even after long-term captivity.

For the new study, a team from the Elephant Reintegration Trust of South Africa examined the behavioral and physiological responses of 11 formerly-captive elephants which had been released onto four different reserves.

For five years each elephant was observed for three weeks at a time at least once annually.

The team looked for indicators that the elephants might be uncomfortable in their wild surroundings and for behaviors that might be “hold-overs” from their time in captivity, such as conflict or confrontation.

The findings showed that, overall, rewilded elephants behaved “very similarly” to their wild neighbors.

Fecal samples collected to test for signs of metabolic stress showed levels within the normal range for wild elephants.

“What I found most fascinating was watching elephants that had spent decades in captivity adapt so successfully to life in the wild,” said co-author Tenisha Roos.

“Seeing them respond to their environment and function much like wild elephants was truly awe-inspiring and a powerful reminder of their remarkable resilience, adaptability, and behavioral flexibility.”

Credit – Glen Carrie / Unsplash

The differences may reflect their previous captive experiences, social circumstances, environmental conditions, and tourism or management pressures, according to the research team.

They say their findings, published in the journal PLOS One, show that rewilded elephants behave “very similarly” to their wild counterparts, despite some consistent differences—suggesting that they have adapted well to their return to wild habitats.

The research team also noted a high degree of variability in behavior between individual rewilded elephants, but that might be related to each animal’s personality.

Each elephant likely found their own unique ways to cope with their relocation.

The 11 animals in the study represent more than 50% of the rewilded elephant population across South Africa so far.

“While a few elephants showed slightly elevated stress biomarkers, all values remained within the normal range for wild populations, indicating successful adaptation—with no evidence of chronic stress.”

Andy Rouse captured antics of Kenyan family of elephants – SWNS

Co-author Tammy Eggeling said: “Although previously-captive elephants may carry the memories of confinement, our research has shown that, when given the opportunity, they can leave that past behind.

“They are able to learn new skills, adapt to unfamiliar environments, and ultimately thrive as wild elephants.”

Co-author Brett Mitchell added: “The data from this project show that when captive elephants are rewilded and given the opportunity, they can regain full autonomy and re-establish natural patterns of movement and behavior.“Through this research, we are also seeing that rewilded elephants can make a meaningful contribution to the conservation of their species.” When Zoo Elephants Are Rewilded in Africa, Here’s How Good Their Coping Skills Are
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Drones are Saving Hundreds of Fawns From Mower Deaths in Germany (WATCH)

Credit: Erika Fletcher

A Bavarian wildlife rescue organization is using thermal imaging drones to locate and rescue vulnerable fawns hidden in tall meadow grass ahead of the annual mowing season.

Every spring, thousands of fawns are killed by mowing machinery across Germany. Baby deer instinctively freeze when threatened, a natural defense mechanism that protects them from predators but leaves them vulnerable to farm equipment.

Traditionally, this work was done on foot—with volunteers walking through the meadows in lines—an extremely labor-intensive task for this volunteer rescue group founded in 2020.

Now, with the thermal imaging of DJI drones, the rescue group, Rehkitz-Rettung Mangfalltal, can locate these hidden animals more quickly and efficiently before mowing begins, especially with the drone’s AI technology features that help pilots reliably spot fawns, baby hares, and ground-nesting birds.

Since integrating drone technology into their workflow, the group’s annual count of rescued fawns has ballooned from 10-15 in previous years to between 300 and 350 fawns today.

In a case study, operators used the Matrice 4 Series’ precision positioning controls to spot heat signatures in vegetation, verify them visually, and direct ground teams to the exact location. (See the video below…)

Whenever the thermal camera detects a heat source, its location is pinned with centimeter-level accuracy using the drone’s GPS and shared instantly with the ground team.

The German case study also provides a video step-by-step guide on the rescue process, including drone operations from an altitude of 80–100 meters and how to handle fawns once they are found.Thanks to the Rehkitz-Rettung Mangfalltal volunteers and drone pilots, farmers are able to happily proceed with mowing—confident that fields have been safely cleared of hidden animals. WATCH the Reuters news video below… Drones are Saving Hundreds of Fawns From Mower Deaths in Germany (WATCH)
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New Species of Monkey Found in DR Congo Shows How Much There’s Left to Discover

Colobus congoensis – credit, released by Daniel Rosengren, Frankfurt Zoological Society

When news reaches the public that a new species has been identified, the chances really are 9 times out of 10 that it’s some deep sea slug or a spider.

From the Congo comes the story of the exception—a new species of colobus monkey has been identified, becoming just the 5th such occasion in 75 years of research on the Colorful Continent.

A pair of Colobus congoensis – credit, released by Daniel Rosengren, Frankfurt Zoological Society

The creature with black fur and an innocent face, also bears a striking set of orange lips.

Named Colobus congoensis and known locally as “Likweli” in its home of Lomami National Park, the monkey had lain hidden from our sight within this remote region of the Congo Basin despite decades of scientific exploration in Central Africa.

The mystery of this new species began with an unexpected sighting in 2008, when researchers captured a partially obscured photograph of the monkey. A decade later, researchers encountered the animal again and obtained a much clearer image. That discovery sparked further investigation into the elusive primate.

Now, new genetic, anatomical, and acoustic analyses have confirmed that the monkey represents a distinct evolutionary lineage that diverged from its closest known relative, the black colobus monkey, 4 to 5 million years ago

“This discovery is both exciting and deeply personal, highlighting the extraordinary biodiversity of my homeland and how much remains undocumented,” said Junior Amboko, a Congolese scientist and co-corresponding author of the findings in a statement.

Smaller than related colobus monkeys—about 15 pounds—it is distinguished by sleek, light-reflecting fur and dramatic facial features created by long black facial hairs and large folded ears. White perianal markings further distinguish this species.

In a separate response to the BBC, Amboko said that the animal had a small range compared to other colobus monkeys, suggesting it could be already Endangered. In the statement, it’s detailed that between 2018 and 2022, researchers recorded 114 sightings across an estimated range of around 900 square miles.

“As part of our search, we interviewed people in 52 villages close to where the animals live. And only people in 8 villages [had ever seen] them.”While the scientists’ official recommendation in their paper describing the monkey is that it should be listed as Endangered, the locals also told them that the monkey was a target of local indigenous hunters. New Species of Monkey Found in DR Congo Shows How Much There’s Left to Discover
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Curious Kids: can spiders swim?

Leanda Denise Mason, Edith Cowan University

Can spiders swim?

Waubra Preschool students, Victoria, Australia

What a great question!

Most spiders don’t swim by choice. But they sure can survive in water when they need to. From floating like a boat, to paddling like a rower, to carrying their own scuba bubbles, spiders have developed brilliant ways to deal with water.

Let’s dive into the science in some more detail, and look at how spiders handle getting their paws wet, with examples from our local bush.

Spiders can run across water

Water has surface tension – this acts like a kind of invisible skin that can hold up small, light objects.

Many spiders are tiny and have water-repellent hairs on their legs, so they can stand or run on water without sinking.

For example, fishing spiders wait at the water’s edge and scuttle across the surface to grab insects, tadpoles or even small fish.

If prey escapes underwater, this spider can even hide beneath the water’s surface briefly, then come back up.

Spiders can hold their breath underwater for days

Spiders don’t have gills, so they can’t get oxygen from water like fish do. But they have evolved clever strategies for staying alive if they stay in the water for a long time.

For example, the Australian Sydney funnel-web spider often falls into backyard swimming pools. People might see one and think it drowned, but it can actually survive underwater for hours by holding its breath much longer than a human could.

That’s because it breathes much more slowly than we do. Like many spiders, it has both tracheae (tiny air tubes) and book lungs (they look like a book with many pages) for breathing. Some spiders can close these and become watertight, to hold their breath for a long time.

Some trapdoor spiders have been recorded only taking a breath every six minutes.

Do not burst their bubble

Some spiders take the air with them like a scuba diver.

On the Great Barrier Reef coast, a little intertidal spider called Desis bobmarleyi actually lives part of its life under seawater. At high tide, it hides in a silk-lined air pocket in coral or shells. It uses the long hairs on its legs and body to trap a bubble around itself so it can breathe underwater between the tides. When the tide goes out, this spider comes out to hunt on the wet reef.

And in other parts of the world, there’s the famous diving bell spider, the only spider that spends its whole life entirely underwater.

It weaves an underwater silk web that it fills with air – like an underwater house. This spider can stay underwater for more than a day at a time by letting its air-bubble vessel actively pull oxygen from the water.

Can you spot Desis bobmarleyi among the corals? coenobita/iNaturalist, CC BY

Flood proofing, trapdoor spider style

Some spiders sit tight and make their homes flood-proof. Remember those trapdoor spiders we mentioned? Trapdoor spiders live snug in burrows underground with a silken lid on top (like a little trapdoor).

In areas that get sudden heavy rains, a trapdoor spider might build its burrow with a raised entrance – a bit like a chimney – so water flows around or over it rather than straight in.

Some Australian trapdoor spiders in the outback clay pans have been found to build thick muddy silk doors that fit perfectly like a bath plug into the surrounding soil. The water just goes straight over the top.

Even if water does get in, some trapdoor spiders can seal their bodies and essentially hold their breath. They don’t swim in their flooded burrows, but they can wait out a flood without drowning.

What to do with a soggy spider

If you ever find a spider struggling in water – say in a swimming pool or even in a bucket – you can help as long as you’re careful.

First, always ask an adult before trying to assist a spider. Nobody has died in Australia in 60 years from spider venom. But some (such as the Sydney funnel-web) can still be fatal, so you must be sure not to touch or provoke it.

A good way to save a spider in a pool is to use a net or a scoop with a long handle. Gently lift the spider out and put it on the ground away from the water. The spider might look dead at first, but don’t be surprised if it “comes back to life” as it dries out – just like trapdoor spiders do.

And remember: never poke a spider with your bare hands, even if it seems lifeless. Spiders such as funnel-webs can still bite underwater or right after being rescued, and they will defend themselves if they feel threatened. So, play it safe and use tools or ask an adult or a spider expert to help.

If anyone is bitten, get an adult to seek medical attention immediately.

Next time you’re exploring nature (or even looking into the toilet), keep an eye out for our eight-legged friends and how they interact with water. You might spot a little spider boat captain or an air-bubble diver right in your backyard.The Conversation

Leanda Denise Mason, Vice Chancellor Research Fellow in Conservation Ecology, Edith Cowan University

This article is republished from The Conversation under a Creative Commons license. Read the original article.

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Sumatran Tiger Cubs Born in the UK Is Huge Win–with Only 400 Left in Wild

credit Tony Kershaw via SWNS

In a valuable milestone for the conservation of the Sumatran tiger subspecies, 3 cubs born to a UK zoo have grown old enough to venture out from the maternity den into the enclosure.

It’s thought there are less than 400 Sumatran tigers remaining in the wilds of Indonesia, and they are considered Critically-Endangered by the IUCN.

Tipah and her litter of cubs – credit Tony Kershaw via SWNS

Howletts Wild Animal Park, in Canterbury, Kent, said the cubs’ births represent an important step forward for the conservation of this cat beyond its natural habitat.

The 3 cubs, 2 girls and 1 boy, were born to first-time mom Tipah and dad Nakal and are just 2 months old.

They were born on April 9th and spent their first few weeks with mom Tipah in their den—but in recent weeks have begun to venture outside to the delight of a photographer there to capture their sensory overload.

“Tipah has taken every step of this journey with calmness, patience and a natural ability to be a fantastic mom,” said Head of Carnivores at Howletts Richard Langston said.

“She spends most of her time up on a platform keeping a watchful eye on them while enjoying a little respite from all the jumping, biting and playing that comes with raising energetic tiger cubs.”

GNN has reported on this cat being born in zoos before—at the Wroclaw and San Diego zoos. It’s considered an important priority animal for captive breeding programs, which have saved many species from extinction in the past.

The park added the cubs were becoming increasingly bold and playful, exploring more of their surroundings and beginning to show their individual personalities.

One cub has already developed an independent streak, often choosing to spend time away from its siblings.

– credit Tony Kershaw via SWNS
  
– credit Tony Kershaw via SWNS
 
– credit Tony Kershaw via SWNS 

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Critically-Endangered Red Ruffed Lemur Triplets Born at Wild Georgia Theme Park

Red Ruffed Lemur Triplets – credit, Wild Adventure Theme Park

A Critically-Endangered lemur couple has welcomed triplets into their lives at a zoo and theme park in Valdosta, Georgia.

It’s the third year in a row the resident female has given birth at Wild Adventures Theme Park, showing how productive captive breeding programs can be, and how much hope one should have about the future of this beautiful species.

The red-ruffed lemur is many things, all of them interesting or beautiful. At 9.5 pounds, it’s one of the largest extant lemurs, while this heft also makes it the world’s largest pollinator.

It’s fuzzy nose is just perfect for snagging a flower’s pollen and sharing it with another as the animal feeds on fruit and nectar. They’re also one of the most fecund of lemurs, capable of giving birth to litters of 6 at a time, and are the world’s only diurnal primate to stow their infants in nests while going out to forage.

Most cling to their mama as she clambers about.

On April 25th, Taylor, Red, and Marjorie came into the world at Wild Adventures Theme Park, lending their spirits to the 590 or so red ruffed lemurs that live in captivity worldwide.

Their parents, Val and Doug, have welcomed a litter of babies every year since 2023. Taylor, Red, and Marjorie are getting along very well with their siblings Swiper, Raven, Beans, and Dennis.

The species is listed by the IUCN as Critically-Endangered, with some 10,000 remaining in the very northern tip of Madagascar in forests that are rapidly disappearing. Successful breeding between pairs like Val and Doug at Wild Adventures help ensure that if those forests can be saved, there will likely always be lemurs around to inhabit them.“Very soon guests will be able to see Taylor, Red, and Marjorie, alongside their parents in their habitat located near the Giraffe Overlook,” said Asher Raymond, a spokesman for the park. Critically-Endangered Red Ruffed Lemur Triplets Born at Wild Georgia Theme Park
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Sampling DNA in Seawater Can Reveal the Health of Dolphin Populations, in First for Conservation

SWNS

DNA floating in seawater is now enough to let scientists monitor the health of America’s dolphin populations.

Sampling DNA in seawater can show the local presence (or absence) of a species, but until now could give little information about those measures of biodiversity that are the most useful in conservation.

But, scientists in the US have now shown that mitochondrial DNA in water sampled near schools of dolphins contains enough information to measure their local effective population size—and monitor the health of these populations.
 
DNA is everywhere in the world’s oceans—not only inside cells from skin, scales, mucous, and feces, but also floating freely. Sequencing such ‘environmental DNA’ (eDNA) from open water has long been used as a cost-effective way of gauging the number and identity of species in a region, especially when they are rare and elusive or living at great depths.

But species richness is only the most basic biodiversity measure. Until now, eDNA-based methods could only give limited insight into the variables that are most relevant for conservation: the number of individuals, the evenness of the abundances of co-occurring species, or their within-species genetic diversity.

But that may be about to change, shows a new groundbreaking study in Frontiers in Marine Science.

“Here we show that repeated eDNA sampling can be used to estimate the genetic diversity of dolphins that occur in large schools and have very large populations,” said corresponding author Dr Frederick Archer from the NOAA/NMFS Southwest Fisheries Science Center in La Jolla, California.

“This is important because genetic diversity, its outcome measure, can be used as a measure of population size and how ready a population is to react to changes in its environment.”

Around Santa Catalina Island, located 47 km off Long Beach, California, the researchers followed 15 schools of dolphins with small boats in 2021. They focused on the four most common species locally: long-beaked common dolphins, short-beaked common dolphins, common bottlenose dolphins, and Risso’s dolphins.

Whenever they encountered a school, the researchers collected two-liter samples of seawater from the surface to compare the mitochondrial eDNA with that in public databases.

The scientists found 836 mitochondrial sequence variants in 126 water samples, of which 76% were from cetaceans and 60% from toothed whales. Overall, 29% were from the species of the school, which had been visually identified.

Long-beaked common dolphins had the greatest genetic diversity, followed by short-beaked common dolphins, while Risso’s and bottlenose dolphins proved much less diverse around Santa Catalina.

“Our study demonstrates the utility [of eDNA surveys] for efficiently assessing and comparing genetic diversity in social odontocetes,” concluded the authors.
Theory holds water

The authors are eager to put their methods to good use in conservation, now that they have been proven to work.

“It would be good to start eDNA monitoring programs as soon as possible that were not possible before. For example, we will be able to see how species composition in very small areas change over the course of a year – including rarer species that we don’t often detect on visual surveys,” said Archer.

“This can give us a lot of information on habitat use and will also allow us to potentially observe how environmental changes and anthropogenic effects such as pollution or underwater sound affect species distributions.” Sampling DNA in Seawater Can Reveal the Health of Dolphin Populations, in First for Conservation
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Birds masturbate, and that’s perfectly normal

Chloe Heys, University of Lancashire; Kevin Arbuckle, Swansea University, and Matilda Brindle, University of Oxford

For captive animals, engaging in natural behaviour is a pillar of the animal welfare framework. But when it comes to sex, one important behaviour has been largely ignored, and sometimes even punished: masturbation.

Solo sex is surprisingly common across the animal kingdom. It is well documented in primates. Tortoises are surprisingly vocal during their solo lovemaking endeavours, if not very graceful. Camels masturbate by rubbing their penises in the sand and porcupines make inventive use of all sorts of objects.

Our new study could change how other scientists view masturbation in birds and improve their welfare.

Masturbation also seems to be common in birds. A quick internet search brings up an abundance of video clips on social media and dedicated posts on bird-keeping forums, largely from worried or bemused hobbyist bird keepers.

It has often been treated as an abnormal problem behaviour in captive birds (particularly parrots). Folklore husbandry has assumed it is the undesirable outcome of stress, bad health or poor environment. Bird keepers often therefore discourage masturbation via punishment or veterinary interventions such as diet or care changes and, sometimes, even drugs and surgery. Despite the welfare implications, masturbation in birds had been largely unexplored by the scientific community.

We set out to change that, by investigating the distribution and evolutionary history of masturbation in birds for the first time. We studied 120 species of bird across 22 major groups, gathering data from the scattered scientific literature, online reports and community forums, and surveys of bird experts.

Our study found that masturbation is widespread across birds with a strong evolutionary history, meaning that it’s an ancient trait probably similar in closely related species. Although we found more records of masturbation in male birds, it occurs in both sexes and across all age groups.

Solo sex also seems to be linked to species that mate with multiple partners, supporting the idea that it might help to increase reproductive success when there is a high degree of competition over fertilisation. For instance, in males it may flush out old sperm to leave newer (better condition) sperm for mating. In females it may increase sexual arousal to help with sneak mating with males other than their partner.

Wild behaviour

Crucially, we discovered that masturbation is actually less common in captivity than the wild, and more common in birds reared by their own parents than by humans. What this tells us is that masturbation in birds is neither an unnatural behaviour, nor a consequence of captivity. Given this finding, it is important that birds are not prevented from masturbation. Of course, as with any behaviour, there may be extreme cases where chronic masturbation could indicate underlying health or husbandry issues.

Avian self-pleasure is usually a rather inelegant affair, in which a bird rubs their cloaca (a shared orifice for both excretion and reproduction) against an object, like a branch, twig or toy. This is often accompanied by a lot of flapping and self-satisfied vocalisation.

One potential reason for the lack of scientific studies exploring avian masturbation may be because the cloaca is thought to have fewer nerve clusters, and therefore lower sensitivity, than our own genitals.

Clearly however, birds are getting some satisfaction from masturbation, so perhaps there is more to a bird’s sensations during sex than has previously been recognised. Further exploration of this could have important implications for both welfare and captive breeding programmes. While sexual pleasure may not be exactly the same experience as for mammals, it is wildly premature to dismiss the idea that birds also feel pleasure.The Conversation

Chloe Heys, Senior Lecturer in Biology, University of Lancashire; Kevin Arbuckle, Senior Lecturer in Biosciences, Swansea University, and Matilda Brindle, Postdoctoral Researcher in Evolutionary Biology, University of Oxford

This article is republished from The Conversation under a Creative Commons license. Read the original article.

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Nest‑building chimpanzees seem to anticipate future weather

Every evening, as they move from place to place through the forest, chimpanzees stop to build a nest – most often in a tree – to sleep in. Using a selection of branches, leaves and twigs, they create comfortable and safe spaces to get some shuteye.

Like human beds, these are places to rest – but they also help chimps stay warm or cool and protect themselves against the weather. As you might expect, how and where chimpanzees build their nests depends on things like temperature, humidity, wind and rainfall.

But how do they make these choices? Previous research has shown the construction is related to the conditions at the time when the creatures are building the nest.

In new research, published today in Current Biology, my colleagues and I show that chimps are a little bit cleverer than you might expect: they seem to build their nests in ways that anticipate what the overnight weather will be.

A year in Rwanda

We conducted a field study on eastern chimpanzees in Nyungwe National Park, Rwanda, a cool and humid mountain forest. Over a 12-month period, we collected detailed data on the structure of nests, the characteristics of their chosen sites, and the kinds of trees the chimps chose.

We also measured how well different kinds of nests insulate against cold and heat. At the same time, we made detailed records of weather conditions when the nests were being built and throughout the night.

This let us test whether chimpanzees respond primarily to immediate environmental conditions, or whether their nesting decisions are better explained by the conditions they experience later during the night.

Chimpanzees are always adjusting their behaviour

Our results show chimpanzees consistently adjust their nesting behaviour in relation to environmental conditions. They preferred to build nests in places that were warmer, more humid and less exposed to wind than surrounding areas.

Nest structure and insulation varied systematically with environmental conditions. In cooler and wetter conditions, nests were thicker and deeper – indicating the chimpanzees put more effort into insulation when conditions are tougher.

We also found that factors such as the width and depth of the nest influenced its insulating ability.

The chimpanzees tended to build more insulating nests when weather was colder and when it was more humid, both during nest-building and overnight.

In cooler and wetter conditions, the chimps also built their nests higher, in taller trees with denser leaf cover. This makes sense: it would be a more stable microclimate with more shelter from rain.

Are chimps thinking ahead?

Importantly, nesting decisions aligned more closely with overnight environmental conditions than with those at the time of construction. When we took overnight weather into account, we found we could explain the variation in nesting behaviour much better than if we used only the current conditions.

One possible explanation is that chimpanzees use environmental cues, such as shifts in temperature, humidity or atmospheric pressure, that are linked to upcoming weather.

These cues may allow them to adjust nest-building behaviour in advance. Does this mean they predict or forecast future weather? Not quite.

But it does show their behaviour is consistent with reacting to environmental signals that are associated with later conditions. Either way, the chimps display a remarkable sensitivity to their environment – and a grasp of how to live in it.The Conversation

Hassan Al Razi, PhD Student, School of Human Sciences, The University of Western Australia

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Mozambique ‘sky island’ expeditions found 4 new species of chameleon – already at risk from forest loss

Male sylvan chameleon (Nadzikambia goodallae) from Mount Ribáuè, Mozambique. Krystal Tolley, CC BY Krystal Tolley, University of Johannesburg

Tropical rainforests are known for their unique biodiversity, with species found nowhere else on Earth. But nearly 30% of tropical rainforest has been destroyed or has become seriously degraded since 1990. Many of these forests have not been fully explored for their biodiversity. This means that the world may be losing species before they are even discovered by modern science.

In Africa, forest loss is rapid; about 25% of the continent’s tropical forest has been lost since 1990, against a backdrop of incomplete knowledge of where the biodiversity is located.

Greatly lagging in this respect are the “sky islands” of northern Mozambique: isolated granite mountains that rise sharply out of the savanna plains. They were left standing when softer rock around them gradually eroded, and can be as high as 3,000 metres elevation. Because they rise so steeply, the sky islands attract clouds and rainfall, feeding moisture to the tropical rainforests on their slopes within an otherwise arid terrain. Isolation has allowed unique species to evolve on each mountain, such as geckos, rodents, fishes, crabs, frogs, butterflies and bats.

Mount Inago. Krystal Tolley, CC BY
Small patch of remaining pristine rainforest at Mount Inago. Krystal Tolley, CC BY

From 2014 to 2018, a research team led by fellow herpetologist Werner Conradie and myself explored these sky island forests to catalogue the species of reptiles found there. We found that each sky island forest is home to a previously unknown species of chameleon within the genus Nadzikambia (forest-dwelling “sylvan chameleons”).

Unfortunately, these chameleons are already at risk of extinction due to the heavy slash-and-burn clearing of the forests, the only place they can call home.

We’ve described these new species, choosing four names to highlight pioneering women scientists whose work inspired us to strive towards new discoveries, but also to call attention to the losses of their forest habitat.

Hunting for chameleons

Over the course of several years, we explored four of Mozambique’s sky islands – Mount Namuli, Mount Inago, Mount Chiperone and Mount Ribáuè – with the aim of cataloguing all reptiles but also in the hopes of finding new species of chameleons. This was because a species of sylvan chameleon had been discovered on one of these mountains during the 1960s, but they were not known from any other mountains.

However, chameleons can be very difficult to find, given their ability to remain camouflaged against the background coupled with their slow movements. They are more easily spotted at night while they are sleeping, as they stand out against the vegetation when illuminated by a strong beam of light. Sylvan chameleons are even more difficult to spot than others, as they usually perch high in the thick forest canopy – tens of metres up.

The search meant dealing with some tough conditions: a long, arduous trek up the hot, arid slopes to reach the forest high up the mountain. Establishing a remote base camp was essential. All food, clothes and gear had to be packed into the camp, and we didn’t know how long it would take to find any animals.

At each of these mountains, we surveyed every night for chameleons – no trails to follow, no GPS signal to guide us, no cellphone signal to call for help.

Sometimes we were lucky and found chameleons on the first or second night. At other mountains we were not so lucky, with fruitless searches making it necessary to return another year.

Eventually these mountains revealed their secrets and we discovered four new species of sylvan chameleon, one on each of the four mountains.

Slash-and-burn clearing of rainforest at Mount Inago. Krystal Tolley, CC BY

We don’t know how big their populations are, but we assume they are in decline. Most of their habitat has been destroyed by forest clearing to make way for agriculture, with increasingly rapid losses in the last decade. We estimate that in some cases, 80%-90% of their habitat has been destroyed.

When parts of an ecosystem are lost, the whole becomes unstable and is eventually lost.

Choosing names for the new species

To highlight their predicament, we have described and named these chameleons and have forecast that three of these species are at high risk of extinction.

In particular, we highlight Nadzikambia goodallae from Mount Ribáuè. This species has been named in honour of the distinguished scientist Jane Goodall, whose own study species, the chimpanzee, is under similar pressures from loss of its rainforest habitat.

Female sylvan chameleon (Nadzikambia goodallae) from Mount Ribáuè. Krystal Tolley, CC BY

We also honour the renowned discoverer of the structure of DNA, Rosalind Franklin, by naming the species from Mount Namuli as Nadzikambia franklinae. The use of DNA data from these chameleons was essential to confirm them as new species.

Nadzikambia franklinae from Mount Namuli. Werner Conradie, CC BY

We have dubbed the species from Mount Inago as Nadzikambia evanescens, meaning “vanishing” in Latin, acknowledging the state of the forest destruction.

Male sylvan chameleon (Nadzikambia evanescens) from Mount Inago. Krystal Tolley, CC BY

The final species, Nadzikambia nubila, is named for the cloudy aspect of Mount Chiperone. This species has a lower risk of extinction given that the local community view the forest as sacred, and say it should be protected.

Female sylvan chameleon (Nadzikambia nubila) from Mount Chiperone. Krystal Tolley, CC BY

This latter case is significant, as it demonstrates that wholesale destruction of these forests is not an essential trade-off for local people to thrive. If encouraged and supported, community support and buy-in can be a solution to protect biodiversity in these sensitive ecosystems.The Conversation

Krystal Tolley, Principal Scientist, University of Johannesburg

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Birds and monkeys in the Amazon share information via ‘internet of the forest’: new research

Ettore Camerlenghi, Deakin University and Ari Martínez, University of California, Santa Cruz

You might go for a walk in the forest to disconnect from work and calm your nerves after a busy week. The chirping and calls of birds in the canopy above might be exactly what allows you to relax.

But what sounds soothing to humans may signal danger to other animals – and trigger fear across the forest.

In our research, published today in Current Biology, we show that when some animals spot a predator they issue a warning cry that is picked up by others and spread through the rainforest canopy. For a time, different species are linked into a shared information network, and parts of the forest briefly fall silent.

Birds and monkeys

During an expedition to a remote area of the Peruvian Amazon, working with a falconer, we used trained raptors to trigger warning calls from birds and primates. We recorded the calls then played them back into the forest and monitored how the community responded.

We already knew that birds sometimes repeat the warnings of others – occasionally even those of different species, or of primates. What we wanted to know was how widespread this behaviour is across the animal community.

Researchers released birds of prey in the Amazon rainforest to study how the alarm calls of other animals travel through the ‘internet of the forest’.

We discovered that alarm calls produced by small bird species – those weighing less than 100 grams – were most often passed on. Other small birds living in the canopy were the most likely to relay the call, but other animals joined in too.

Larger species, including capuchin and spider monkeys, sometimes responded as well. Two canopy species in particular – the black-fronted and the white-fronted nunbirds – stood out as especially likely to repeat and propagate the warnings of their neighbours throughout the forest.

Sounds and silence

Alarm calls from species living in the forest understorey were far less likely to spread and be propagated by other birds or primates.

However, even when these alarm calls were not repeated, they changed the forest’s soundscape. Small canopy birds almost completely stopped singing after hearing a predator alert. At the same time, animals in lower forest layers often continued to make sounds despite the perceived threat.

Together, these findings suggest that the Amazonian canopy is not only the rainforest’s most mysterious layer – largely unexplored and home to much of its biodiversity – but also functions as an information highway, like a fibre-optic network through which animals rapidly share signals of danger.

A new layer of the ‘internet of the forest’

In the past decade, the idea of an “internet of the forest” has become popular through the concept of the “wood wide web”, where plants exchange resources and information via root systems and fungal networks. Our work points to another communication system, one operating high above the ground.

Suspended above our heads is a vast ecosystem where animals constantly listen to one another, forming an eavesdropping network that spreads critical information within seconds.

The vocal activity of birds is usually associated with finding mates and defending territories. However, we now know that sometimes this activity, or lack of it, may represent pulses of a soundscape of fear.

Next time you walk through a rainforest, look up and listen to the birds. A sudden silence may mean a raptor is gliding somewhere above the canopy.The Conversation

Ettore Camerlenghi, Associate Research Fellow, Avian Behaviour, Deakin University and Ari Martínez, Assistant Professor of Ecology and Evolutionary Biology, University of California, Santa Cruz

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Spectacular New Species Found in Cambodia’s Limestone Caves–Asia's 'Little Laboratories'

A new species of pit viper found living in the caves – credit, supplied by Fauna & Flora ©

A breathtaking expedition high among limestone escarpments and deep in the cave systems they contain has revealed several new reptile species, including a dazzling pit viper you have to see to believe.

Exploring over 60 caves across 10 hills in the Battambang province, western Cambodia, the survey uncovered a treasure trove of extraordinary creatures besides, many found nowhere else on Earth.

The survey was led by Fauna & Flora International in collaboration with Cambodia’s Ministry of Environment and field experts. The team identified 6 new geckos, 2 micro-snails, and 2 millipedes in addition to the viper.


They also confirmed the presence of many threatened species in the landscape surrounding the caves—such as the Sunda pangolin, Indochinese silvered langur, long-tailed macaque, and green peafowl, further highlighting the critical need to protect this habitat.

Karst covers 20% of the Earth’s landscape. This soluble bedrock made of limestone has created some of the most spectacular rocky landscapes on Earth—including the upturned egg cartons shapes along the great South China Karst, Ha Long Bay in Vietnam, Tsingy de Bemaraha in Madagascar, The Burren in western Ireland, the world’s largest wellspring in Vrelo Bune, Bosnia, the Cenotes of the Yucatan, in Mexico, and Mammoth Cave in the US.

The susceptibility of karst to erode from rainfall has seen it carved into a million beautiful and dramatic shapes that often play host to microclimates where threatened animals can thrive.

Landscapes along the Li River amid the South China Karst – credit, Sam Beasley via Unsplash

Dr. Lee Grismer, a professor of biology at La Sierra University in the US, was part of the expeditionary team, and spoke to F&F about the importance and uniqueness of the landscape.

“Each one of these isolated karst areas act as their own little laboratory where nature is performing the same experiment over and over and over independently. The results are species that exist nowhere else—not just nowhere else in the world, or that country—but in no other cave.”

The Shiva Gecko – credit, supplied by Fauna & Flora ©

Indeed, caves from easily in karst landscapes, and many of the world’s longest and largest—and least-explored—cave systems are found in East and Southeast Asia.

This is certainly the case in Battambang, where the survey team had first to ascend the steep forested slopes of the karst outcrops before scrambling and squeezing through crevices and crawlspaces to reach the cave systems.

Inside, they documented a rich array of life, both endemic to the caves and others—like a big reticulated python—who were just visiting. While the chatter of the Endangered silvered langur troupe, faded behind them, the team began encountering animal after animal that had never been described by science.

A spectacular new species of pit viper (from the Trimeresurus genus) was collected during the survey and is currently being described. Recognized by their triangular heads, these highly venomous snakes track down their warm-blooded prey using the heat-sensitive pits behind their nostrils.

4 populations of the striped Kamping Poi bent-toed gecko were found and identified as a new species: Cyrtodactylus kampingpoiensis. Despite being described as just one species, it is thought that, due to the geographic isolation of the karst formations, these 4 populations are on separate evolutionary trajectories, and further genetic analyses may reveal whether they are in fact 4 different species instead of 1.

Another new species of gecko was named after the Hindu god of destruction: Shiva.

In a statement, Fauna & Flora International said it is working with local partners to help conserve Cambodia’s karst landscapes, epitomized through the recent release of guidelines for sustainable development and management of cave ecosystems.

The Fauna & Flora International expeditionary team – credit, supplied by Fauna & Flora ©

The guidelines integrate international best practices with Cambodian context, providing practical measures to safeguard bat colonies, preserve rare and endemic cave biodiversity, promote sustainable guano harvesting and ensure responsible tourism development.

“Cambodia’s karst areas are a treasure trove of scientific secrets waiting to be uncovered,” said Sothearen Thi, Karst Biodiversity Coordinator at Fauna & Flora in the statement.“But, without sustainable management, we may never find out what these areas truly hold. Karst landscapes are facing many human-driven challenges, and biologically significant species could go extinct before they have even been discovered. We are working with the Cambodian government and local partners to increase protection of the landscapes, with sustainable management being the number one priority.” Spectacular New Species Found in Cambodia’s Limestone Caves–Asia's 'Little Laboratories'
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Endangered Cahow, One of the Rarest Seabirds in the World, Hatched on Nonsuch Island in Bermuda

A Bermuda petrel, or Cahow, on Nonsuch Island – credit, Cahow Recovery Project

Though an event neither singular nor inaugural, the hatching of an endangered seabird and national icon of Bermuda is still being celebrated wildly by a special group of conservationists who’ve created a “living museum” on Nonsuch Island.

Measuring just 14 acres and found in the northeast corner of the Bermuda island chain, Nonsuch Island is the only place the world’s 3rd-rarest seabird, known locally as the cahow, comes to breed.

The fact that it is breeding at all is nearly a miracle, as the cahow was believed to be extinct for a period of 300 years that started in the early days of British colonial governance and extended all the way to the second-half of the 20th century.


The animal, also known as a Bermuda, or gadfly petrel, bears all the quirks of an animal doomed to follow the dodo into history. It takes 3-6 years for adults to return to Nonsuch Island to breed, and if they do, the female may produce one egg.

That one egg may hatch, although it might not; some 50% of the eggs don’t hatch. Adults abandon that single chick one-week before it fledges, when instinct drives it to seek food out at sea while still learning how to fly. Between 28 and 35% of fledglings don’t survive their first year.


Nesting on the ground, they’re extremely vulnerable to predation from invasive animals, and in 1960, British ornithologist and Bermuda’s first conservation officer, David Wingate, identified just 18 breeding pairs on Nonsuch Island.

Wingate would go on to pioneer the Cahow Recovery Program, which today is recognized as one of the most successful restoration projects anywhere in the world for a Critically-Endangered species.

By the time Wingate’s successor as chief of the program, Jeremy Madeiros, took over, their numbers had grown to 55. Today, there are 450 birds of all ages on the island, a remarkable turnaround.

Part of that turnaround was making sure these birds had good nesting habitat. Cahows nest in underground burrows or deep rock crevices; only nests deep enough to be completely dark are chosen.

Today, 85% of all cahows nest in artificial concrete nest burrows constructed for them as part of the Recovery Program.

The recovery program gestated a transformation of Nonsuch Island into a complete wildlife sanctuary, wooded, and with a small freshwater marsh where access to the public is strictly limited to prevent invasive species introduction. The restoration of the once barren island into a ‘Living Museum of pre-colonial Bermuda’ was Wingate’s life’s work.

65 years into this rewilding experiment, key endemics have repopulated the island, including the yellow-crowned night heron, West Indian top shell, land hermit crabs, and the beautiful Bermuda skink.Expeditions there are organized by the environment ministry for educational and research purposes, while several live camera feeds allow those interested to observe the cahow in its natural habitat. Endangered Cahow, One of the Rarest Seabirds in the World, Hatched on Nonsuch Island in Bermuda
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24 New Species Including a New Family of Amphipods Identified in Deep Sea Survey

Collage of the 24 new Amphipod species identified in Clarion-Clipperton Zone – credit, National Oceanographic Center, Southampton

A recent international survey of a deep sea zone near Mexico turned up 24 species of shrimp-like animals called amphipods, including a whole new taxonomic family, called Mirabestiidae.

The survey took place in the Clarion-Clipperton Zone (CCZ) between Hawaii and Mexico, where a fractious seabed can range in depth from 10,000 to 20,000 feet.

Over 10,000 species of amphipods have been described by science, yet they’re such a diverse order of animals, an expedition such as this can still scoop out handfuls of new ones—and in all different colors too.

“To find a new superfamily is incredibly exciting, and very rarely happens so this is a discovery we will all remember,” said Dr. Tammy Horton of the UK’s National Oceanographic Center (NOC) in Southampton.

“With more than 90% of species in the CCZ still unnamed, each species described is a vital step towards improving our understanding of this fascinating ecosystem.”

The NOC was joined by partners and aspiring scientists from all across Europe, as well as New Zealand and Canada, for a weeks-long taxonomy workshop organized at the University of Lodz, Poland, led by Dr. Anna Jażdżewska.

Location of the Clarion Clipperton Zone – credit USGS

The expedition and workshop were organized under the International Seabed Authority’s Sustainable Seabed Knowledge Initiative (SSKI) which aims to describe 1,000 new species by the end of the decade in order to possess a better understanding of deep-seabed biodiversity when making decisions about deep-sea mining.

“The team’s findings provide information that is crucial for future conservation and policy decisions, and it highlights how important it is for this work to continue,” Dr. Jażdżewska said in a statement.

Stretching 1.7 million square miles across the eastern Pacific Ocean, the CCZ was discovered by the Scripps Institution of Oceanography in 1954. It’s been an extremely well-surveyed area of the deep seabed, though that in itself isn’t saying much, and indeed 42% of all known deep sea species were first described in the CCZ.

The expedition uncovered a new family, called Mirabestiidae, and even a new superfamily Mirabestioidea, revealing completely new evolutionary branches. Two new genera were also discovered: Mirabestia and Pseudolepechinella.

For readers who lack a mental flowchart of taxonomy hierarchies, one famous family from above sea level is Felidae, containing all cats wild and domestic. Felidae is nested inside of the superorder Feliformia, which in addition to all the cats, contains civets, hyena, mongoose, and the curious fossa of Madagascar.

Two genera nested inside the family Felidae are Panthera, containing the tiger and the lion, and Lynx.

In the CCZ, students and professors alike reveled in pulling up one new species after another, before taking them back to a frigid Poland for analysis.Creatures were named in honor of both Horton and Jażdżewska, the organizers of the expedition and workshop, while others named species after relatives, impressions from the experience, and even a video game character that one of the amphipods resembled. 24 New Species Including a New Family of Amphipods Identified in Deep Sea Survey
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Surgeons Perform First-Ever Surgery for Critically-Endangered Monkey Weeks Before She Gave Birth

Chester Zoo via SWNS

GNN often stays abreast of births among the Chester Zoo’s incredibly diverse residents of rare and endangered species, but few have ever been cuter or rarer than this Roloway monkey.

Chester Zoo is one of only two places in the UK that Roloway monkeys can be found, a spokesman said, and the breeding population there supports the animal as conservationists ponder what to do to ensure it can survive in its West African home.

The mother is named Masaya, and before the 15-year-old primate gave birth to a daughter named Lagertha, she was the first ever Roloway monkey to undergo surgery in captivity—to remove a golf-ball sized abscess from her foot.

Masaya had to have one toe amputated during the procedure, which was done at the University of Liverpool’s Small Animal Teaching Hospital.

“Masaya is a very experienced mom and she’s parenting magnificently,” said
Zoe Edwards, primate keeper at Chester Zoo. “The fact Masaya’s foot has healed so well is a huge relief. If she’d had a [full] amputation, we’d have been left with real questions about whether she could hold her offspring or continue with her normal behaviors.”

Roloway monkeys originate from West Africa and are listed as Critically-Endangered by the International Union for Conservation of Nature (IUCN). Once common in the lush rainforests of Ghana and the Ivory Coast, the Roloway monkey now survives only in isolated pockets of old-growth forest.

The baby’s name is Lagertha – credit, Chester Zoo via SWNS

Masaya at the Liverpool Vet. Hospital where she underwent surgery – credit, Chester Zoo via SWNS

Chester Zoo witnessed the first birth of a Roloway monkey in captivity in 2020, and Lagertha is the 3rd to be born since then. Edwards said it marked an important moment in the species’ conservation. There are only a few breeding females in zoos in Europe, and only one other in England at the Yorkshire Wildlife Park.

Masaya had experienced recurring problems with her foot since she came to the zoo in 2023. It was determined to be an abscess, and when the swelling worsened in 2025, the decision was made to take Masaya to Liverpool for a CT scan.

“It’s not every day you take a monkey to vet school,” said Charlotte Bentley, Veterinary Officer at the zoo’s Animal Health Center. “Following the scan, we decided an operation was the way forward.”

According to the New England Primate Conservancy, the Roloway monkey is now considered one of the most urgently threatened primates in the entire world. A big-bodied monkey, they have been hunted to such small populations that, ironically, they’re now considered too uneconomical to pursue anymore, and so have inadvertently gained a short respite from poaching.

he conservancy admits that the most likely chance for survival is for breeding programs like the one at Chester to continue the propagation of the species until such a time as their native forests in Ghana and the Ivory Coast can be appropriately and reliably protected from poachers and logging. Surgeons Perform First-Ever Surgery for Critically-Endangered Monkey Weeks Before She Gave Birt
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