Saturday, September 05, 2026

 

Understanding women's biology could reshape the future of heart disease research



Women have long been underrepresented in cardiovascular research, while biological sex differences remain poorly reflected in models of the heart's arteries. A new ERC-funded project at Aarhus University aims to help close this knowledge gap



Aarhus University





When a woman develops heart disease, it is not always the same disease - or driven by the same biological mechanisms - as in men.

Some cardiovascular diseases occur almost exclusively in women. Others present with different symptoms, develop differently or are associated with different risk factors.

This is no coincidence. Part of the explanation is that women have historically been underrepresented in cardiovascular research. But according to Monika Colombo, Associate Professor at Aarhus University, that is only half the story.

"Fortunately, we have become much better at including women in clinical research. But we are still not very good at incorporating the biology that makes women and men different into the models we use to understand cardiovascular disease. That is the fundamental knowledge we are still missing," she says.

Colombo now hopes to address that challenge through DISSEX, a research project awarded a prestigeous €1.5 million ERC Starting Grant under the European Union's Horizon Europe programme.

The project will investigate how hormones, stress and genetic factors influence women's coronary arteries and develop new models to explain why certain cardiovascular diseases affect women differently from men.

Why does an artery suddenly become vulnerable?

Researchers already understand a great deal about how blood flows through the coronary arteries and the mechanical forces acting on the vessel wall.

What they understand far less well is how the body's own biological signals influence the cells that make up those blood vessels.

How do hormonal changes affect the strength of an artery throughout life? What role does physical and psychological stress play? And how do genetic factors interact with the mechanical forces that arteries experience every second of every day?

Current scientific models can only partly answer those questions.

Through DISSEX, Colombo's team will bridge biology and biomechanics. By combining laboratory experiments, advanced medical imaging and computational modelling, the researchers will investigate how biological signals gradually alter the properties of blood vessels—and how those changes may eventually make an artery vulnerable to rupture.

"Today we can measure hormones and we can study the shape of blood vessels. What we still lack is an understanding of how the body's biology changes the cells within the vessel wall over time. That is the missing connection we are trying to uncover," says Colombo.

A disease that exposes a wider knowledge gap

The project focuses on Spontaneous Coronary Artery Dissection (SCAD), a condition in which a spontaneous tear develops within the wall of a coronary artery.

SCAD predominantly affects women, many of whom have none of the traditional risk factors associated with cardiovascular disease.

Simon Winter sees these patients in his clinical work. He is a consultant cardiologist at the Department of Cardiology at Gødstrup Regional Hospital and a clinical professor at Aarhus University, and serves as an advisor to the project.

"We see younger women coming in with what initially looks like a heart attack, but the underlying cause is not the usual build-up of plaque in the arteries. Instead, a tear develops in the artery wall, which can obstruct the flow of blood. It is a serious condition that can strike relatively early in life, and it can also take a considerable psychological toll on patients," he says.

This is precisely why SCAD challenges our current understanding of cardiovascular disease.

If clinicians are to become better at identifying who is at risk, understanding the mechanics of blood vessels alone is not enough. They also need to understand how hormones, stress and genetic factors shape the biology of the artery wall throughout a person's life.

To achieve this, the researchers will study living human coronary artery tissue and combine those findings with patient data and advanced computational models. Their goal is to uncover the biological mechanisms that gradually make an artery more susceptible to dissection.

"This is an area where we still lack fundamental knowledge. We need to understand why the condition occurs. Are some artery walls particularly vulnerable? Do hormones play a role? Or is it the result of several factors interacting? If we can identify markers and gain a better understanding of how the disease develops, we may also become better at knowing what to look out for in our patients," says Simon Winter.

From fundamental biology to more precise cardiovascular medicine

In the longer term, the researchers aim to develop personalised rupture-risk maps of the coronary arteries.

By integrating knowledge about hormones, genetics and biomechanics, they hope to identify patients at increased risk earlier and provide clinicians with better tools for diagnosis, monitoring and treatment planning.

For Colombo, however, the project's significance extends well beyond a single disease.

She hopes DISSEX will help reshape how researchers investigate women's cardiovascular health more broadly.

"If we want precision medicine, we also need models that reflect the biological diversity of patients. Women's cardiovascular physiology should not simply be regarded as a variation of a male standard. It deserves to be understood on its own biological terms," she says.


Aarhus University is home to several major initiatives focusing on women’s health. Here are five examples:

  • The research project Women’s Health and Well-being is conducting Denmark’s largest-ever study of women’s health and well-being, including a survey of 300,000 women.
  • PREG-AID investigates how medicines used to treat autoimmune diseases affect both mother and child during pregnancy.
  • The FEMaLe project uses artificial intelligence and health data to improve the detection and treatment of endometriosis. The project has helped raise awareness of the disease in both Denmark and the EU.
  • The BIOSFER project investigates the reasons behind declining fertility and explores how biological, social and psychological factors contribute.
  • The Women’s Health Network brings together researchers and other stakeholders to strengthen research into women’s health.

How new moms cope with stressful news may matter more than the news itself, study finds



By Tracy DeStazio



University of Notre Dame

Kristine Joy Chua 

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Kristine Joy Chua, a biological anthropologist in the University of Notre Dame’s Department of Anthropology.

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Credit: University of Notre Dame






The everchanging social, political, and economic landscape in many countries has become more tenuous and intense in recent years. Respondents in a 2026 report from the World Economic Forum indicated a prevailing mood of uncertainty, with 50 percent of them anticipating a turbulent or stormy outlook on life over the next two years. This negative perception swells to 57 percent of respondents when looking ahead to the next 10 years.

Social structures, government policies, and cultural norms shape how people think, live, and interact. If those factors are in constant flux, the repercussions can have adverse effects. More worrisome, however, is how external stressors affect pregnant women, who are already experiencing significant physiological changes in preparation for the birth of a baby and, subsequently, adjusting to life with a newborn.

If there are additional factors in a mother’s own life—such as violent, turbulent, or uncertain social or political circumstances—then her fear and anxiety will likely increase, potentially putting her and her unborn child’s health at risk. The impacts of these sociopolitical stressors could lead to preterm birth, among other complications, not to mention the psychological and physiological effects.

“Yet, we know very little about how mothers cope with these stressors,” said Kristine Joy Chua, assistant professor in the Department of Anthropology at the University of Notre Dame. Chua researches reproductive biology, maternal health, and health inequities, particularly within Filipino communities and communities of color.

This gap motivated Chua and her fellow researchers to ask the question: How do expectant mothers manage these uncertainties and cope with sociopolitical stressors? The answer became the focus of their recently published study in the journal Social Science and Medicine, of which Chua was the lead author.

Interviewing 21 pregnant Filipina women across multiple regions of the Philippines in 2021, Chua and her team sought to understand how these women internalized such stressors. They found that they used creative coping strategies, some of which are grounded in Filipino cultural practices and shaped how they navigated such uncertainties. Some reframed difficult circumstances and maintained a positive outlook, while others deliberately disengaged from political stressors and focused instead on the well-being of their families.

What causes stress and where does it come from?

According to Chua and her co-authors, previous research had been limited in that it did not address how pregnant individuals perceive and embody outside stressors and the implications for health. Nor did it address the various coping strategies they found useful in dealing with stress in order to protect their bodies and pregnancies.

The research team specifically chose to study pregnant women in the Philippines, a country marked by intense state violence, high poverty rates, political corruption, and a highly publicized war on drugs, as well as some of the world’s strictest COVID pandemic lockdown restrictions during the research period.

Their interviews with the pregnant women revealed how interconnected social, political, and economic stressors can be—with 67 percent of study participants citing financial stress, 38 percent indicating access to quality medical care, and 52 percent saying cultural pressures affected their emotional, physical, and mental well-being.

One of the societal challenges compounding this predicament for citizens of the Philippines is their outsized reliance on social media for gathering news and information—an open portal that has the potential to continuously feed them negative or politicized discourse. According to Chua and her co-authors, 62 percent of their study participants cited Facebook or other social media sites as their primary source of information, adding that the “news they ingested had a profound impact on their perceived stress levels.”


Pregnant mom in the Philippines 

Artwork by Elissa Chudzicki/University of Notre Dame

What are some ways new moms cope?

The interviewees revealed that not all of the negative news they consumed necessarily affected them adversely. Many described relying on creative coping strategies pulled from within their Filipino identity and upbringing.

For example, noted the researchers, many expectant mothers found ways to reframe those stressors. One way to accomplish that is through the concept of “community viewing”—comparing oneself to others to determine who might be “doing better.” The realization that others within their circle might actually be relatively worse off (experiencing death, food scarcity, and extreme poverty, for example) allowed them to manage the difficulties of their own situations.

Second, maintaining a positive outlook on life and being able to “laugh things off” gave them a new perspective and renewed state of mind that enabled them to ‘build resiliency against adversity.”

Another reframing technique many expectant moms found useful was looking toward their relationships with family members and appreciating the positive aspects of their lives. Said one study participant: “We cope by remembering the blessings we have [now] and that are yet to come.”

Chua said that participants also found ways to exercise their own agency, which could manifest in one of three cultural practices. One is disengaging and remaining indifferent or resistant to the news of the day—letting the negative news “go in one ear and out the other,” as one participant described.

A second method is to invoke the mentality of bahala na—a phrase that translates to “whatever happens, happens” and is driven by a belief that God will provide. In other words, they believe that regardless of how difficult things are or how far out of their control the situation may become, these new moms and their families will somehow prevail.

Finally, respondents found outright avoidance to be a surefire way to leave some of those stressors behind and move forward with daily living. Deliberately staying silent—as opposed to engaging in political debates or trying to change others’ political opinions—allowed them to protect themselves against unpleasant, negative, and stressful experiences during pregnancy, the co-authors wrote. Rather, they focused “on concerns within their immediate control,” such as the current safety and health of their children and the general well-being of their families.

Chua emphasized that “the intent of the work is not to romanticize what might be viewed as a passive outlook or response, but to investigate the strategies these women have at their disposal to cope and deal with challenging circumstances. Doing so is harmful to the participants and to the field of study.”

What can these findings mean for other mothers?

While these specific coping strategies were utilized by the pregnant Filipina women included in Chua’s study, their insights may extend to any expectant mother living with social, political, and financial stressors.

“Maternal and fetal health is influenced not only by medical care but also by the broader social and political environment,” Chua said. “And politics definitely plays a significant role in shaping perinatal health.”

Chua said the research highlighted how further work is needed to fully understand this interaction, as well as how these coping strategies affect stress biology during pregnancy and its impact on newborn health. “Future study also needs to take into account how helpful or harmful these coping strategies may be,” she added.

“Our study is one of the first to examine how Filipina women embody politics during pregnancy,” the co-authors wrote. “We expect these findings to contribute to the advancement of women’s health on a local and global level by demonstrating the complexities associated with stress embodiment, management, and its impact on fetal development.”

Contact: Tracy DeStazio, associate director of media relations, 574-631-9958 or tdestazi@nd.edu

 

Younger brains recover better than older brains after traumatic injury, right? Maybe not




Texas A&M University






Conventional wisdom holds that younger brains are better equipped to recover from injury. Their greater flexibility allows them to adapt, rebuild connections and compensate for damage in ways older brains often cannot. But recovery can mask harmful changes that continue unfolding beneath the surface. New research from Texas A&M University suggests that same flexibility may come with an unexpected downside.

The findings, published in Experimental Neurology, challenge long-held assumptions about recovery after traumatic brain injury (TBI) and illuminate neural pathways that may also contribute to later cognitive decline.

Using laboratory models of TBI, researchers discovered that younger brains may be more vulnerable to the processes that lead to post-traumatic epilepsy, a chronic seizure disorder that can emerge months or even years after an injury. Older brains showed fewer signs of epilepsy but were vulnerable to neuroinflammation, circuit remodeling and memory loss — changes relevant to brain injury-induced dementia.

“People may assume younger brains are more resilient after injury, but our findings suggest the story is much more nuanced,” said Dr. Samba Reddy, Regents Professor and Distinguished Professor of neuroscience and experimental therapeutics at the Texas A&M Naresh K. Vashisht College of Medicine and senior author of the study. “The same plasticity that helps younger brains adapt may also create conditions that support the development of seizure-producing networks.”

Post-traumatic epilepsy follows different paths in younger and older brains

Despite decades of research, scientists still do not fully understand why some injured brains develop epilepsy, memory problems or other lasting neurological complications while others do not.

To better understand the role of age, the research team monitored brain activity continuously for four months following traumatic injury, tracking changes in neurological function, cognition and brain structure. The results revealed two very different patterns.

“Older brains that developed seizure activity tended to do so earlier after injury, but the seizure activity stabilized and remained relatively limited,” said Reddy, who directs the Texas A&M Institute of Pharmacology and Neurotherapeutics. “Younger brains followed a delayed trajectory. Seizure activity emerged later but increased steadily over time, resulting in a significantly greater overall seizure burden during the long-term phase of recovery.”

Younger brains also showed higher levels of electrical activity associated with the development of epilepsy, Reddy said.

Better recovery in some areas, worse outcomes in others

The study found that age did not simply make outcomes better or worse; instead, it appeared to shift where vulnerabilities emerged after injury.

Older brains showed quicker improvements in motor function and coordination following traumatic injury. Younger brains, by contrast, continued to exhibit deficits in balance and coordination long after the initial trauma.

Yet the opposite pattern emerged when memory was tested.

Older brains displayed greater difficulties with long-term memory retention, even when learning appeared relatively intact. Younger brains also experienced cognitive deficits, but the decline in memory performance was more pronounced in older subjects.

“Aging changed the path of recovery rather than simply making recovery more difficult,” Reddy said. “Older brains appeared less susceptible to chronic seizure activity, but they remained vulnerable in other ways, particularly when it came to memory and cognitive function.”

Brain rewiring holds the answer for dementia

To understand why age influenced the brain’s response to injury so differently, researchers examined changes in the hippocampus, a region involved in both memory and seizure generation.

Surprisingly, the two age groups showed comparable levels of neuron loss after injury. That finding suggests that cell death alone can’t explain the stark differences seen after injury. Instead, the differences appeared to be linked to how the brain reorganized itself after trauma.

“We found that younger brains showed greater levels of electrical hyperactivity associated with epilepsy, while older brains demonstrated stronger signs of abnormal circuit reorganization and persistent inflammatory responses in specific regions of the brain,” Reddy said.

Taken together, the findings suggest that the long-term consequences of TBI are shaped less by the amount of damage sustained and more by how the brain responds to that damage over time.

In addition to revealing more about post-traumatic epilepsy, Reddy said the research provides insights on the development of dementia and related memory issues in aging brains. The study identifies persistent inflammation, circuit reorganization and memory deficits as warning signs that deserve closer scrutiny as possible links between brain trauma and later neurodegeneration, Reddy said.

Age-specific treatments may matter

TBIs affect millions of people each year. Their serious consequences may emerge long after the injury appears to have healed, such as seizures, memory loss or dementia-like decline. Yet many efforts to prevent long-term complications have largely treated patients as though they follow the same recovery process. The new findings suggest that assumption may overlook critical biological differences.

“A younger brain may require interventions aimed at preventing the gradual development of seizure-producing networks,” Reddy said, “while older brains may benefit from approaches that address memory loss, inflammation and cognitive decline following injury.”

He said the results reinforce the idea that age is not just a demographic characteristic but an important biological factor that influences how the brain heals after injury. “Understanding those differences could help us develop more targeted strategies to reduce seizures, preserve cognitive function and improve long-term outcomes for patients.”

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By Lesley Henton, Texas A&M University Division of Marketing and Communications

 

Hidden DNA in medieval gospels reveal history of deadly livestock virus




University College Dublin

Epistles of St Paul, Cover 

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Cambridge, Trinity College, MS B.10.5, fol. 62v, the Epistles of St Paul, Ireland/Northumbria, 700–800 CE. Reproduced with kind permission of the Master and Fellows of Trinity College Cambridge

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Credit: Cambridge, Trinity College, MS B.10.5, fol. 62v, the Epistles of St Paul, Ireland/Northumbria, 700–800 CE. Reproduced with kind permission of the Master and Fellows of Trinity College Cambridge





Some of Europe’s most well-known historic manuscripts, including the York Gospels, have proven to be biological time capsules for uncovering the 3,500-year history of the sheeppox virus (SPPV).

By extracting DNA from the animal skins used to make the documents’ centuries-old parchment, an international team of geneticists, historians, virologists, protein chemists and conservators, led by University College Dublin have provided the first genetic evidence of how this devastating disease plagued European farmers’ herds long before the modern era.

A highly contagious disease, sheeppox spreads rapidly and can affect large portions of a flock in a short time.

The disease is particularly dangerous because it can cause very high mortality rates, especially in young animals, and dramatically reduces productivity by damaging wool, meat and milk yields.

“The recording of ancient DNA of pathogens has completely changed our understanding of infectious disease in the past, and here we show that parchment can also preserve animal pathogen DNA. It is possible that archives and libraries around the world also contain the genetic traces of disease outbreaks in animals in the past,” said Louis L’HĂ´te, PhD candidate at UCD and lead author of the study. 

“These genomes help us understand how these pathogens evolved and how they impacted past societies - such as sheeppox virus, which we show has been affecting Eurasian sheep herds for at least three and a half millennia.”

In a new study, published in Science Advances, reconstructing over 3,500 years of sheeppox virus evolution, researchers identified traces of the disease in medieval manuscripts, including several of significant historical importance.

Among the works analysed was the 1,000-year-old York Gospels, one of the finest illuminated manuscripts surviving from the early Anglo-Saxon period, and earlier manuscripts such as the Corpus Glossary of Corpus Christi College Cambridge, one of the earliest English dictionaries, and other medieval codices from across Britain and continental Europe.

In several cases, multiple pages from the same manuscript were found to contain sheeppox virus DNA, indicating that infected animals were used in their production.

Because the parchment used in the making of these documents was made from the hides of livestock like sheep, goats, and cattle it serves as a unique bio-archive, preserving the health of the animal at the time of its death centuries ago.

One of the most unexpected findings from the new study was the detection of sheeppox virus on parchment made from calfskin and goatskin, suggesting either rare examples of cross-species infections or that there was contamination during the parchment-making process.

“Parchment making has been considered a vanishing craft, but we are beginning to understand just how much of the past it has retained. This project shows that parchments not only preserve our cultural history for hundreds of years, but also the landscape of disease in our livestock  in the medieval period,” said Dr Kevin G. Daly, Associate Professor at UCD School of Agriculture and Food Science and the study’s supervising author.

“This kind of exciting, surprising discovery is only possible when researchers from a range of disciplines come together to share their expertise and data - a generosity and trust that collaborative science depends on.”

By combining the study of manuscripts with even older samples from Bronze Age sheep teeth, the study reveals that Sheeppox has threatened livestock for over 3,700 years.

Unlike other skeletal material, teeth can preserve genetic evidence of infection over thousands of years, providing a valuable record of past outbreaks.

The research team identified the earliest known detections of sheeppox virus from dental remains recovered from ancient pastoralist settlements in the Eurasian steppe.

By comparing these ancient sequences with modern ones, they  estimate that the major lineages of capripoxviruses (sheeppox virus, goatpox virus, and lumpy skin disease virus) diverged between 11,500 and 3,700 years ago. 

This timeline aligns with the rise of animal domestication and the major translocation of sheep from the steppe into Europe.

“People around the world are still fighting against this pathogen - there is currently an outbreak of sheeppox in Greece, causing much economic damage,” said Louis L’HĂ´te.

“Ancient genomes can help us understand how these pathogens affecting us today evolved. We find that unlike the smallpox virus, the sheeppox virus genome was very stable over the last few millennia.”

Adding: “This might mean that genetic changes before this point were very important to how the sheeppox virus evolved to infect its host, which may help us fight the pathogen in the future.”

This study was funded by Taighde Éireann-Research Ireland and the European Research Council, and led by researchers at UCD in collaboration with over 30 Irish and international institutions including Trinity College Dublin, the Helmholtz Institute for One Health, Université Paris 1 Panthéon-Sorbonne, the University of Leicester, Cambridge University, and the University of Copenhagen.


Cambridge, Trinity College, MS B.10.5, fol. 62v, the Epistles of St Paul, Ireland/Northumbria, 700–800 CE. Reproduced with kind permission of the Master and Fellows of Trinity College Cambridge

  

Cambridge, Trinity College, MS B.10.5, fol. 62v, the Epistles of St Paul, Ireland/Northumbria, 700–800 CE. Reproduced with kind permission of the Master and Fellows of Trinity College Cambridge

Credit

Cambridge, Trinity College, MS B.10.5, fol. 62v, the Epistles of St Paul, Ireland/Northumbria, 700–800 CE. Reproduced with kind permission of the Master and Fellows of Trinity College Cambridge

 

Decades-old museum specimens reveal ten extraordinary new worms



International research team mines museum collections to solve 147-year-old evolutionary mystery




University of Göttingen

One of the many types of sponges that have been found to act as hosts to branching worms. 

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One of the many types of sponges that have been found to act as hosts to branching worms. This one is called Crateromorpha meyeri and it is a deep-sea, glass sponge found in Okinawa, Japan. In this close up of its main opening it is possible to see semi-transparent threads: an example that the newly identified genus of branching worm, Cladosyllis, is living inside.

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Credit: Naoto Jimi





Scientists have discovered that one of the most unusual creatures in the animal kingdom is far more diverse and evolutionarily complex than previously known. An international team led by the University of Göttingen has reconstructed the evolutionary history of branching marine worms – rare annelids that live hidden inside sea sponges and whose bodies branch repeatedly into multiple posterior ends. Until now, only three species of branching worms have been identified. By combining DNA sequencing of museum specimens with newly collected specimens and detailed anatomical analyses, the researchers discovered ten new species and solved a long-standing puzzle dating back to the nineteenth century. The results were published in the Zoological Journal of the Linnean Society.

 

Branching worms are among the strangest animals known to science. Unlike typical worms, they possess a single head that gives rise to a tree-like network of branches. These species live in symbiosis with and inside sponges, where their unusual body architecture allows them to spread throughout their host. Using genomic data obtained from both newly collected specimens and decades-old museum material, the researchers found that branching worms form a distinct evolutionary group comprising two major lineages: one group belongs to the genus Ramisyllis, while the second was assigned to a completely new genus, Cladosyllis. “Our findings would have been impossible without access to valuable museum specimens. These collections are not just repositories of old samples, but resources that continue to generate new discoveries,” said Professor Maria Teresa Aguado, Scientific Curator of the Biodiversity Museum at Göttingen University and leader of the study.

 

The researchers also found a remarkable level of hidden diversity, which had remained undetected for more than a century despite these worms being present in a huge part of the world’s oceans. The team identified thirteen distinct forms of branching worms, including at least ten likely new species distributed across the Indo-Pacific, the Red Sea and New Zealand. The study suggests that specialization on different sponge hosts played a key role in driving diversification and evolution: some species inhabit deep-sea glass sponges at depths of up to 1,000 metres, while others live in shallow-water sponges.

 

“For over a century, the rare branching worms were all classified as a single widespread species. However, we have shown that – like their bodies – their family tree has many branches, each closely associated with its own sponge species and located in specific areas,” said Dr Guillermo Ponz Segrelles, coauthor of the study. Beyond solving the puzzle of how to classify these creatures, the research provides new insights into the evolution of animal bodies. The study demonstrates that all branching worms descended from a common ancestor, meaning that their extraordinary body architecture evolved only once. The researchers also discovered that, despite their overall similarity, the two major lineages produce their branches in different ways, highlighting the developmental flexibility that can arise during evolution.

 

“Some of the sponges hiding these worms came from the Senckenberg collection and date back to 1914,” notes Dr Ekin Tilic at the Senckenberg Research Institute and Natural History Museum Frankfurt and co-author of the study. “We were able to reveal the worms without damaging the sponges by using microCT imaging – modern techniques are helping us rediscover hidden biodiversity in centuries-old collections.” The researchers believe that many more branching worm species remain undiscovered and that these animals could be an important model for studying the evolution of complex body forms, symbiosis and biodiversity in marine ecosystems.

 

Original publication: Aguado et al (2026). Many Branches, One Lineage: Museomic Insights into the Diversity and Evolution of Branching Syllid Worms. Zoological Journal of the Linnean Society. DOI: 10.1093/zoolinnean/zlag120


Petrosia sponge found in a coral reef of Mayotte, in the Indian Ocean – one of the many types of sponge that can be a host to bizarre branching worms.

Credit

Nicole de Voogd

Cutting-edge 3D X-ray imaging techniques allowed researchers to create cross-sectional images of the sponge Crateromorpha without damaging this unique museum specimen, which was collected in 1914 from Sagami Bay, Japan. The image shows details of the longitudinal section, with the sponges’ stem internal space occupied by a branching worm from the newly identified Cladosyllis genus. The white arrow points at the worm which lived inside its host sponge.

Credit

Ekin Tilic and Maria Teresa Aguado Molina