Monday, June 15, 2026

 

Goosebump moments in archaeological research


How people lived centuries ago: This volume explores their identity


University of Bonn

Jun.-Prof. Dr. Alice Toso 

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from the Bonn Center for ArchaeoSciences.

 

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Credit: Photo: Bernadett Yehdou/University of Bonn





How did people live centuries ago? How did they see themselves? How were they perceived by others? Today, archaeology uses modern methods to examine skeletons, personal belongings, burial practices, material culture and social and spatial relationships. The book “Human Identities in the Archaeological Record: Interdisciplinary Perspectives from Late Antiquity to the Modern Period” shows how past identities can be reconstructed from this evidence.

“Identity is an extraordinarily timely topic,” says co-editor Jun.-Prof. Dr. Alice Toso of the University of Bonn’s Center for Archaeological Sciences. “We all experience identity as something shaped by belonging, difference, memory, social expectations, and personal decisions.” The scholar is fascinated by the question of how people in the past may have understood themselves and how they were perceived by others.

Of course, researchers can never fully understand people from the past. They must always be careful not to impose their own categories on them. “The possibility of reconstructing something of a person’s experiences, affiliations, or struggles after such a long time gives me goosebumps,” says the bioarchaeologist from the University of Bonn. “For me, this sense of human connection across centuries is one of the most powerful aspects of archaeological research.”

Co-edited by Annamaria Diana (Independent researcher, Ireland), Daniela Marcu-Istrate (Vasile Pârvan Institute of Archaeology, Romania), and bioarchaeologist Alice Toso (University of Bonn), “Human Identities in the Archaeological Record” brings together international perspectives on belonging, diversity, resilience, and otherness from Late Antiquity to the modern period.

Science Across Borders

Using innovative analytical methods, researchers can investigate what people ate, where they grew up and how their bodies were affected by disease, diet, work, and inequality. However, the editors emphasize the importance of a transdisciplinary approach: “Large datasets remain incomplete as long as they are not interpreted within the archaeological context, using historical evidence and incorporating social science theories”, says Diana.

Diet is an excellent example of the complexity of this research. “What a person ate depended not only on their personal preferences,” says Toso. Rather, it was also shaped by the landscape and the resources available there, as well as by religious regulations, agricultural practices, access to markets, political power, household structures, and social status.

Interpreting a burial is just as complex. “A grave does not simply express the identity of the deceased”, says Marcu-Istrate, senior researcher at the Vasile Pârvan Institute of Archaeology in Bucharest, “it also reflects the decisions of relatives, religious authorities, and the wider community.” Thus, the location, design, grave goods, and treatment of the body reflect the relationships between the individual, the community, and social institutions.

Which identities are concealed?

The fundamental question addressed by the book is how people understood themselves and others. But also, how these identities were expressed, negotiated, imposed, altered, or suppressed. “Every person is both unique and part of one or more communities” says Diana. The volume examines how individuality coexisted with collective affiliations based on religion, social status, occupation, ancestry, gender, origin, or political identity.

The researchers are asking how reliably identity can be reconstructed from material remains. Archaeological evidence is incomplete, and historical sources are often fragmentary and shaped by elite perspectives. Whose identity becomes visible, and who is forgotten or deliberately erased? “Archaeology can recover evidence of enslaved people, migrants, religious minorities, social outsiders, and communities that are absent from written history,” says Toso, who is also a member of the Cluster of Excellence “Bonn Center for Dependency & Slavery Studies” as well as the transdisciplinary research areas “Life & Health” and “Present Pasts.” “Reconstructing identity is therefore also an ethical responsibility.”

Drawing on case studies from Europe, America, Africa and Australia, the book illustrates how people and communities expressed, negotiated, and preserved their identities in various historical contexts. It is surprising how relevant these archaeological questions are today. Many of the chapters address migration, displacement, religious persecution, colonialism, and the suppression of cultural diversity. “The past reveals both the long history of these processes and the resilience of communities whose identities were preserved despite the pressure to conform”, says Marcu-Istrate.

Publication: “Human Identities in the Archaeological Record: Interdisciplinary Perspectives from Late Antiquity to the Modern Period,” Bloomsbury Academic, 288 pp., 46 black-and-white illustrations, 120 US-Dollar


Ancient millipedes still had secrets to tell


Researchers completed the first evolutionary history of Earth’s first land animals, pushing their origins tens of millions of years deeper into the past.


Virginia Tech

millipede 

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Hirudicryptus canariensis (left) Siphoniulus neotropicus (microscopic image at right) are the two rare millipedes whose DNA helped researchers complete the first evolutionary history of all living millipede orders.

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Credit: Photos by Rafael Garcia and Paul Marek for Virginia Tech.




Long before vertebrates walked on land, millipedes had the place to themselves.

Hundreds of millions of years before dinosaurs arrived, these early decomposers were helping establish Earth's terrestrial ecosystems. But despite their ancient history, scientists still hadn't fully unraveled their evolutionary story.

Now, a Virginia Tech-led team of international scientists has solved one of the last major mysteries in millipede evolution, revealing new clues about a group of animals that helped pave the way for life on land.

The findings, published in Current Biology, complete the first evolutionary history of all living millipede orders. By combining genomic data from living species with morphological evidence from fossils, researchers traced the group's origins to nearly 460 million years ago — suggesting millipedes may have been present long before the oldest known millipede fossils.

"Millipedes beat vertebrates onto land by more than 80 million years," said Paul Marek, the study’s lead investigator and associate professor in the College of Agriculture and Life Sciences’ Department of Entomology. "They really set the stage for later life on land, including humans and vertebrates."

Reconstructing the missing pieces

For more than a century, scientists knew that two rare groups of millipedes — Siphoniulida and Siphonocryptida — existed, but without fresh specimens for DNA analysis, they couldn't confirm where they belonged in the millipede family tree. 

One of the groups includes millipedes barely a centimeter long that spend their entire lives underground. The other survives in just a few known locations. 

"These last two were kind of like our white whales," Marek said.

Researchers traveled to Los Tuxtlas, Mexico, and Spain's Canary Islands to collect Siphoniulus neotropicus and Hirudicryptus canariensis, two millipedes whose DNA had never been included in an evolutionary analysis.

"It took 10 people over a week just to find this one tiny 10-millimeter adult," said Luisa "Fernanda" Vasquez-Valverde M.S. '21, Ph.D. '24, the paper's first author and an assistant in Marek's lab. “Finding them in the field was hard because we were just seeing this little white nematode. We didn’t know for sure it was a millipede until we looked under the microscope." 

By sequencing DNA from the two groups, comparing hundreds of genes across 82 millipede species, and combining those results with evidence from 29 fossils, researchers were able to determine where the groups fit in millipede history and when their lineages emerged. The effort generated terabytes of genetic data and relied on Virginia Tech's Advanced Research Computing resources to reconstruct relationships stretching back hundreds of millions of years.

One group, Siphonocryptida, turned out not to be a distinct order after all, but part of an existing lineage. The other, Siphoniulida, was finally placed among its closest relatives on the millipede evolution timeline. 

Colonizing an alien Earth

The analysis revealed that millipedes may have originated nearly 460 million years ago — roughly 35 million years before the oldest known millipede fossils and much earlier than previously believed.

"The biggest surprise was just how ancient some of these lineages turned out to be," Marek said.

Back then, life on Earth looked dramatically different. Marek said millipedes helped pioneer life on land by breaking down organic material and recycling nutrients in some of the planet's first ecosystems.

"There were no vertebrates, no trees, no leaves, no flowering plants, no plants with seeds," Marek said. "Millipedes were feeding on decaying mosses, decomposed slime, and primordial gunk on the surface of the Earth."

The completed family tree also helped reveal when one of millipedes' most important adaptations first emerged. 

"They made the first chemical weapons," Marek said. “They're little chemical factories.”

The study traces those chemical defenses to about 260 million years ago, providing the clearest picture yet of when millipedes first developed them.

Unheralded heroes of the ecosystem

Today, millipedes remain among nature's most important detritivores, breaking down decaying plant material and returning nutrients to ecosystems. 

"It's really kind of puzzling that they have such an important function in the ecosystem, and yet they're so poorly known," Marek said. 

For all that scientists have learned, millipedes still hold many new discoveries. Scientists have described more than 14,000 millipede species worldwide, but experts estimate there could be tens of thousands still undiscovered. Marek and his students have helped identify new millipedes in locations ranging from Virginia Tech's Blacksburg campus to the city of Los Angeles.  

For a new generation of millipede researchers like Vasquez-Valverde, that's part of what makes the animals so compelling.

"There is all this potential for discovery," she said. "It keeps me wondering what else we're going to find." 

The research, funded by the National Science Foundation, also included scientists from the Field Museum of Natural History, Hampden-Sydney College, Universidad de La Laguna, Virginia Tech’s School of Plant and Environmental Sciences, the Australian National Insect Collection, West Virginia University, and Universidad Autonoma del Estado de Hidalgo.

 

Global study confirms mosquito nets remain a powerful weapon against malaria – but warns their long-term effectiveness is under threat



“Mosquitoes are developing resistance and adapting their behaviour,” experts warn




Taylor & Francis Group





A major analysis of 25 studies across Africa and Asia finds that insecticide-treated nets cut malaria cases by up to 68% — but highlights challenges that threaten to undermine their long-term impact.

The study, published in the peer-reviewed journal Infectious Diseases, confirms that insecticide-treated nets (ITNs) continue to provide strong protection against malaria – but reveals that their effectiveness varies considerably between regions and communities.

These findings suggest that the performance of this relatively simple, low-cost intervention is under pressure — particularly in areas where insecticide resistance is already established.

The researchers warn that without locally adapted control strategies that combine ITNs with other mosquito control measures, progress made over recent decades could be at risk.

“While this study reinforces that ITNs remain one of the most powerful weapons we have against malaria, it is also a warning that we cannot afford to become complacent,” says Dr Gbeminiyi Otolorin, a doctoral researcher at James Cook University, Australia, and a veterinary public health clinician and researcher in the Faculty of Veterinary Medicine at the University of Jos, Nigeria.

“Mosquitoes are developing resistance and adapting their behaviour – and a tool that works well in one place may already be failing in another. We must continuously monitor, evaluate and tailor our control strategies as we strive towards global elimination of the disease.”

Malaria is a life-threatening disease caused by a parasite transmitted to humans through the bites of infected mosquitoes. In 2024, there were an estimated 282 million cases and 610,000 deaths from the infection worldwide. ITNs are among the most widely used and cost-effective tools in malaria prevention – protecting individuals while reducing mosquito populations and cutting transmission across entire communities.

In order to get a better understanding of how much insecticide-treated nets truly reduce malaria illness and death, the researchers analysed data from 25 experimental studies comparing ITN performance with no nets. These included 19 studies examining malaria incidence and six assessing malaria-related deaths, spanning eight African and four Asian countries. Study populations included children under five, pregnant women, households, and entire communities, with follow-up periods ranging from two months to five years.

The findings confirm the strong protective effect of ITNs across these diverse settings. In Asia, ITNs were associated with a 68% reduction in malaria cases and an 18% reduction in malaria-related deaths. In Africa, they reduced malaria incidence by between 29% and 40%.

However, the researchers also identified considerable variation in the effectiveness of ITNs between studies, particularly in Asia. They suggest these differences may be influenced by complex local factors — including mosquito species diversity, patterns of insecticide resistance, and community compliance with net use.

“ITNs are undeniably an effective tool that has saved millions of lives and will continue to do so — but relying on them alone is not enough, particularly in areas with established insecticide resistance,” adds Dr Otolorin, a specialist in infectious disease epidemiology.

“Integrated strategies that combine nets with other interventions should now be considered essential – otherwise we risk losing ground in the fight against a disease that still kills hundreds of thousands of people every year.”

The paper calls for further research evaluating long-term net durability, community compliance, and insecticide resistance patterns.

“My hope is that this work adds to the existing evidence base supporting malaria control efforts and contributes to ongoing discussions around how insecticide-treated nets can be improved, adapted, and used effectively in communities where malaria prevention remains a priority,” Dr Otolorin concludes.

ARACHNOLOGY

Devoted dads and citizen science: the evolution of parental care in harvestmen is uncovered



The Linnean Society of London
Amazochroma (photo John Uribe) 

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Amazochroma spider guarding eggs

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Credit: John Uribe





Citizen science data from popular platform iNaturalist has helped uncover the evolution of parental guarding behaviour in harvestmen, as shown in research published in the Zoological Journal of the Linnean Society.  

Combining nearly three decades of fieldwork with data from iNaturalist, an international team of researchers led by a scientist from the University of São Paulo have more than doubled the number of documented cases of parental care in harvestmen. As a result, the evolution of maternal and paternal care in the superfamily Gonyleptoidea was reconstructed for the first time.  

The study has found that parental guarding behaviour has evolved, disappeared, and then re-emerged several times throughout the evolutionary history of harvestmen. By mapping this behaviour, researchers found that maternal care evolved only from no care, a pattern also seen in insects. However, paternal care was shown to evolve from either no care or from maternal care, suggesting different selection pressures were at play. The researchers theorised that when paternal care evolved from maternal care, it is likely evidence of a sexually selected behaviour; a hypothesis known as ‘enhanced fecundity’.  

With over 6900 species currently recognised, harvestmen represent one of the most diverse orders of arachnids in the world. Despite accounting for only 0.6% of arthropod diversity, they represent over half of the independent origins of paternal care, a rare trait in the animal kingdom. This offers a unique opportunity to study the evolutionary development of parental care on a broader scale.  

Lead author Glauco Machado explained: “It’s very rare in nature, paternal care, and this behaviour evolved many times independently. So, by looking at harvestmen we can explore questions related to the factors that led to the evolution of this behaviour. In many species where males care for the offspring alone, the caring activity is a sexually selected behaviour, which means that females prefer males that are caring for the eggs.” 

Citizen science allows anyone to lend their time and curiosity to projects around the world, without the need for specialist knowledge. From recording garden bird populations for the RSPB as part of their ‘Big Garden Bird Watch’, rediscovering a lost species of grasshopper in Australia and even uncovering an ancient writing system in cave art, citizen science data has proven to be an expanding resource in modern research.  

Inspired by a talk on utilising citizen science in bird research, Machado and his team made use of global citizen science database iNaturalist, where users can upload georeferenced observations of organisms found across the world, to expand their dataset. The rate of data collection from iNaturalist has proven to be much faster than traditional scientific work. Between 1936-2025, scientific literature documented parental guarding behaviour in 80 species of harvestmen; this study more than doubled this number, with 62 records coming from iNaturalist alone. Machado and his team were able to do this in only two days.  

The significance of iNaturalist reaches far beyond expanding datasets. Machado stresses that its true value lies in the accessibility of this resource to scientists worldwide.  

“It’s a tremendous source of information that can improve the velocity with which we accumulate biological information. I would never be able to do this by visiting museums around the world. It would be very expensive, very time consuming, but here we conducted the search in only one week.” 

By removing access costs and the need for timely and expensive fieldwork, citizen science platforms are transforming traditional research and opening opportunities for large scale research by scientists in the Global South.  

The study also highlights the importance of taxonomists in modern research. While citizen science platforms can amass huge amounts of data very quickly, Machado emphasises that taxonomic expertise is still necessary to correctly identify the species and recognize the sex of the caregiving individuals.  and distinguish between superficially similar behaviours such as parental care vs mate guarding. 

“I think taxonomists’ role in modern science is more important than ever. We cannot preserve a species that doesn't have a name. And names are provided by taxonomists. So, it's very important.” 

Though a remarkable breakthrough, the study doesn’t come without its limitations. Sampling bias remains a challenge in parental care studies, for the simple fact that it’s easier to record instances of parental care than of no care. Yet, the authors argue that studies such as this one are filling major gaps in our knowledge regarding the presence/absence of care. Given more than half of records in this study were new, Machado hopes that scientists continue to explore the use of citizen science platforms in future.  

“I think it's a very broad contribution for people that are working with insects, frogs, and all kinds of groups, animal groups, in which we have both maternal care and paternal care.” 

Deltilagus (photo Glauco Machado) 

Deltilagus spider guarding eggs

Credit

Glauco Machado


Quindina (photo John Uribe) 

Quindina spider guarding a nest

Credit

John Uribe)

 

Study reveals 45 new toxins produced by bacteria associated with foodborne infections




Computational tools were used to analyze the genetic material of 6,165 samples from 149 different types of Salmonella enterica subspecies





Fundação de Amparo à Pesquisa do Estado de São Paulo






 Researchers at the University of São Paulo (USP) in Brazil have discovered 45 new toxins produced by Salmonella bacteria, some of which are associated with foodborne infections. The study was conducted at the Center for Research in Bacterial and Bacteriophage Biology (B3 RIDC) and was published in the journal PLOS Biology. It shows that these substances primarily act in the competition among microorganisms for space and resources. The study also suggests that these substances may inspire the development of new antibiotics, in-depth studies with humans, and biotechnological applications in the future.

The B3 is one of the Research, Innovation, and Dissemination Centers (RIDCs http://cepid.fapesp.br/en) supported by FAPESP.

To investigate the microscopic arsenal used by the pathogen, the team analyzed genetic data from Salmonella and its type VI secretion system (T6SS), which is a spear-like system that the bacterium uses to inject effectors, such as toxins that interfere with the functioning of other cells, into the environment or directly into competing microorganisms. Using computational tools, the team analyzed the genetic material of 6,165 samples from 149 different serovars of Salmonella enterica, identifying potential toxins and comparing sequences among different bacteria. They also inferred their functions based on similarities to known proteins.

A total of 128 types of toxins were identified, 45 of which were very different from any known toxin and had never before been described by science. “This result implies that the diversity of bacterial toxins and antitoxins worldwide is very high, with new varieties emerging or diverging radically from known related variants,” explains Robson Francisco de Souza, leader of the bioinformatics group at the Laboratory of Protein Structure and Evolution at USP, a researcher at the B3 RIDC, and one of the authors of the study.

The identified molecules act in different ways. Some compete with other bacteria, while others affect eukaryotic cells, including those of fungi, yeasts, algae, and even mammals. “It’s possible that some of them play a direct role in human infections, but to confirm that hypothesis, we’d need to identify which strain carries the genes targeting eukaryotes and experimentally assess their effect on cells and infection,” the researcher notes.

This diversity is also reflected in the distribution of the effectors discovered among the different Salmonella groups. The article shows that each group has a unique combination of molecules secreted by the T6SS. This suggests that the bacterium selects and maintains specific effectors based on environmental pressures. “The evolution of these systems and this diversity are driven by both gene recombination, which frequently occurs to generate and activate new toxins, and by natural selection, which, in a scenario of biological conflict, fuels an arms race among bacteria,” states Souza.

The data also suggest that Salmonella subgroups collected from natural environments have a greater number of effectors than those collected from patients. This indicates that toxin diversity increases in contexts with a greater variety of competitors. “This happens because, as new challenges and adversaries emerge, the microorganism needs to develop new tools to excel in these disputes over resources,” the researcher explains.

According to Souza, these findings should improve our understanding of bacterial competition strategies and pave the way for new clinical and biotechnological applications. “We may even have applications that we can’t yet anticipate,” he predicts. “We believe this because some of our previous work has shown that important eukaryotic proteins originated from bacterial toxins,” he adds, highlighting the potential of these compounds in different biological contexts.

Souza emphasizes that the field is far from exhausted. “Bacteria such as Salmonella, Acinetobacter, and other organisms still offer opportunities to understand the role of these toxins in ecological interactions,” he states. “We’re continuing to invest in developing software and pipelines to automate this type of analysis and expand the investigation to new lineages, such as archaea and lesser-known bacteria, which present even more opportunities for this type of discovery,” he concludes.

About São Paulo Research Foundation (FAPESP)
The São Paulo Research Foundation (FAPESP) is a public institution with the mission of supporting scientific research in all fields of knowledge by awarding scholarships, fellowships and grants to investigators linked with higher education and research institutions in the State of São Paulo, Brazil. FAPESP is aware that the very best research can only be done by working with the best researchers internationally. Therefore, it has established partnerships with funding agencies, higher education, private companies, and research organizations in other countries known for the quality of their research and has been encouraging scientists funded by its grants to further develop their international collaboration. You can learn more about FAPESP at www.fapesp.br/en and visit FAPESP news agency at www.agencia.fapesp.br/en to keep updated with the latest scientific breakthroughs FAPESP helps achieve through its many programs, awards and research centers. You may also subscribe to FAPESP news agency at http://agencia.fapesp.br/subscribe

 

Research forecasts global antimicrobial resistance threats for next two decades



Research led by King’s College London has analysed antimicrobial resistance (AMR) on a global scale to predict how resistance patterns could evolve by the year 2050, identifying around 210 resistance traits that could pose the greatest future risk.





King's College London





AMR is considered one of the most urgent global public health threats, with experts predicting AMR could cause 39 million deaths between 2025 and 2050. AMR is not a single problem, and instead involves many different genes, pathogens, hosts and environmental factors.

The new study, published in Cell Genomics, used machine learning and forecasting to identify which genetic factors or ‘traits’ linked to AMR in pathogens are most likely to become future threats, and which may decline over time. Understanding which AMR traits are most likely to spread could help target future interventions and investment towards the highest-risk threats.

The researchers analysed 16 bacterial species identified by the World Health Organization (WHO) as critical priority pathogens, including Klebsiella, Acinetobacter and Escherichia coli, which are associated with high mortality and limited treatment options.

The research analysed data collected from across 127 countries and involved three main stages. First, researchers analysed over 45,000 genomes from the 16 bacterial species and AMR data using machine learning to identify which resistance genes were genuinely linked to antibiotic resistance.

Secondly, the team examined more than 1,000 environmental, health and socioeconomic indicators, including poverty, climate and healthcare trends, to understand how these global factors may change in the future.

Finally, the researchers linked these global trends with resistance patterns to identify which antimicrobial resistance traits are most strongly associated with future environmental and socioeconomic changes, allowing them to forecast the resistance threats most likely to grow by 2050.

Analyses revealed 210 pathogen-specific AMR traits projected to increase by 2050. These resistance traits were then narrowed down to 32 high-risk threats based on factors including their presence in WHO priority pathogens, their ability to move between bacteria, and their occurrence across multiple hosts. These 32 threats were strongly linked to future spread and associated with key drivers including mortality, poverty, healthcare access and population density.

Socioeconomic inequality and living conditions, such as overcrowding and access to sanitation, emerged as major predictors of increasing AMR. The study also highlights that the highest-risk resistance mechanisms are often highly mobile, allowing them to spread rapidly between bacteria, animals and humans.

Professor Tania Dottorini, Professor of Artificial Intelligence in Science at King’s College London and senior author of the paper, said: “Our research uses a multi-scale, multi-modal approach that has never been applied in this way before. By identifying which resistance traits are increasing, where they are spreading, and what is driving them, we can better target surveillance, policy and interventions towards the threats that are most likely to impact global health in the future.

“Reducing antibiotic use alone won't be enough. Tackling AMR requires structural interventions on inequality, sanitation, nutrition and health equity alongside stewardship. We believe that our findings provide a roadmap for targeted AMR interventions.”

The researchers hope that the findings will help guide future global surveillance strategies and support more targeted approaches to tackling AMR.

The study was supported by funding from UKRI through the Medical Research Council, Biotechnology and Biological Sciences Research Council and Innovate UK, in partnership with French National Research Academy (ANR), Swiss National Research Foundation (SNSF), Fondazione Regionale per la Ricerca Biomedica (FRRB) as part of the international Joint Programming Initiative on Antimicrobial Resistance (JPIAMR).

Sadhana Sharma, BBSRC AMR lead, said: “This important study demonstrates the value of a whole-systems approach, integrating genomics, advanced machine learning and global socioeconomic data to better understand the complexity of antimicrobial resistance patterns.

“By identifying the resistance traits most likely to emerge by 2050, it supports a shift from reactive to proactive action, helping to direct resources towards the highest-risk threats.

“By recognising where these risks are concentrated, we can better coordinate efforts to mitigate what remains one of the most serious threats to global public health.”