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Remote fieldwork and museum collections reveal hidden pit viper diversity in High Asia

Published in ZooKeys, a recent study revises the Himalayan pit viper group using a combination of fresh and historical DNA, morphology, skeletal anatomy, and ecological observations.

The high mountain ranges of Asia remain among the least biologically explored regions of the continent. Now, an international team of researchers has shown that one of their most elusive venomous snakes, long treated a single species, is in fact a complex of five distinct species, three of which are new to science.

Published in the open-access journal ZooKeys, the study revises the Himalayan pit viper group using a combination of fresh and historical DNA, morphology, skeletal anatomy, and ecological observations. The data reveals that what scientists had long treated as a single widespread species, the Himalayan pit viper first described in 1864, actually consists of multiple deeply distinct evolutionary lineages.

The analyses identified five clearly distinct species-level lineages, i.e. the Himalayan pit viper in the strict sense, Gloydius chambensis described in 2022, and three previously unrecognised species from different parts of Pakistan and Nepal. Alongside genetic divergence, these lineages exhibit distinct morphological and skeletal variations.

Phylogeny and distribution of five pit viper species in the Himalaya and Hindu Kush. Image credit: Dr Daniel Jablonski

“These mountain systems still harbour overlooked vertebrate diversity and hold important clues to the biogeography of Asia,” says Daniel Jablonski of Comenius University Bratislava, who has been conducting extensive research in Pakistan and Afghanistan for many years.

“By combining modern field sampling with data from historical museum specimens, we uncovered evolutionary lineages that had remained hidden for more than a century after the original description of the Himalayan pit viper.”
Daniel Jablonski

A key element of the discovery was the integration of newly collected material with a powerful source of evidence: DNA extracted from museum specimens collected in the 19th and early 20th centuries. This included the original type specimen of the Himalayan pit viper, allowing the researchers to clarify the identity of the species in its strict scientific sense.

The study underscores the enduring scientific value of natural history collections. Indeed, specimens gathered by earlier generations of explorers and preserved in museums are still helping scientists solve modern biological puzzles, especially in regions where fieldwork remains difficult.

Paratype of the newly described species Gloydius hindukushensis from northwestern Pakistan. Image credit: Dr Daniel Jablonski and Dr Frank Tillack.
Paratype of the newly described species Gloydius nepalensis from Nepal. Image credit: Dr Daniel Jablonski and Dr Frank Tillack.

In fact, part of the discovery had been waiting in plain sight. “Museum specimens are not just records of the past. They are active research tools and essential infrastructure for future science,” says Sylvia Hofmann from the Museum Koenig as part of the Leibniz Institute for the Analysis of Biodiversity Change, who has comprehensively worked in the Himalaya and Tibetan Plateau during the past 20 years.

“Some of the key evidence had been sitting in museum collections for more than a hundred years. We just didn’t have the tools to recognise it. As analytical methods continue to improve, the scientific value of these collections will only grow and revealing biodiversity we didn’t even know was there.”
Sylvia Hofmann

Representatives of the herpetofauna play an important role in the ecosystem, particularly as ecological indicators, within the food chain, and as predators in pest control. A group of top predators in the region consist of pit vipers adapted to mountainous environments, which have so far been studied only very inadequately in the Himalayan region.

“Our work aims to close these gaps in knowledge and to lay the groundwork and provide inspiration for further, in-depth studies on this ecologically and medically relevant group.”
Frank Tillack of the Museum für Naturkunde Berlin, Leibniz Institute for Evolution and Biodiversity Research

Tillack maintains close ties with Nepalese colleagues and has been collaborating with them for 35 years on projects concerning the biodiversity of herpetofauna in the Himalaya.

An important part of the study is the osteology of these snakes, including the skull anatomy of the lectotype BMNH 1946.1.19.64 of *Gloydius himalayanus*, collected more than 160 years ago.
Image credit: Kristin Mahlow-Tillack.

The study also emphasises how much remains to be discovered in regions that have long been difficult to access for scientific research. “Pakistan’s high mountains are still full of biological surprises,” says Rafaqat Masroor of the Pakistan Museum of Natural History, the country’s leading herpetologists.

“This finding highlights how little we still know about a region long shaped by socio-political instability.”
Rafaqat Masroor

Beyond taxonomy, the findings also carry an important conservation message:

“Each of the newly recognised species seems to occupy a relatively restricted range in fragile mountain environments, highlighting new ecological and evolutionary questions.”
Daniel Jablonski

Without recognising such diversity, it would be impossible to assess it accurately or protect it effectively.

Original study:

Jablonski D, Tillack F, Mahlow-Tillack K, Petzold A, Wilzo M, Das A, Idrees M, Baniya CB, Masroor R, Hofmann S (2026) Integrative taxonomy reveals previously undescribed diversity within the Gloydius himalayanus complex (Squamata, Viperidae, Crotalinae) from the Himalaya and Hindu Kush. ZooKeys 1280: 83-153. https://doi.org/10.3897/zookeys.1280.182768

Revealing the Invisible: A New Baseline for Salish Sea Diatoms Answers a Global Call

A new checklist published in the Biodiversity Data Journal sheds light on the diversity of diatoms in the Salish Sea.

Invisible to the naked eye, phytoplankton play a critically important role at the base of marine food webs, yet their diversity continues to be underestimated. Recently, the UN Global Compact released “The Plankton Manifesto,” highlighting how these microscopic organisms are crucial for addressing the “triple planetary crisis” of climate change, biodiversity loss, and pollution. Diatoms, a major group of photosynthetic microalgae, are particularly powerful in driving roughly 20% of global photosynthesis and forming the very base of marine food webs.

Yet despite their monumental importance, microalgal ecosystems remain largely unexplored and poorly mapped. That is why a recent major scientific undertaking in the Northeast Pacific is so significant.

A First-of-its-Kind Baseline in the Salish Sea

sample locations from the Salish Sea — Map of sampling locations. A Distribution of sampling sites throughout the Salish Sea (green markers).Red frame: area of enlargement around Galiano Island (1B); B Sampling sites around Galiano Island (green markers). Map credit to Webber et al., 2026.

Diatom records of the Salish Sea bioregion have historically been fragmentary, dating back to early inventories in the 1800s, and with only scattered surveys filling the gap across the 20th and 21st centuries. As Andrew Simon, PhD student at the University of Alberta, president of IMERSS, and one of the study’s researchers, puts it:

The Salish Sea has long been studied for its rich marine biodiversity. Yet, until now, the history of research on its primary producers has been fragmented, and we have lacked a consolidated baseline record.

Now, for the first time, researchers have taken a significant step toward closing that gap. A team of Canadian researchers — Mark Webber (University of Victoria; IMERSS), Elaine Humphrey (UVic; IMERSS), Arjan van Asselt (IMERSS), Alice Chang (UBC), Evan Morian (Hakai Institute; UBC), and Andrew Simon (IMERSS; University of Alberta) — has published a new checklist of 924 diatom taxa alongside a curated dataset of 11,469 records in the open-access journal Biodiversity Data Journal, providing a long-needed foundation for environmental monitoring across this region of the northeast Pacific Ocean.

Trigonium quinquelobatum, external valve view. SEM. Scale bar: 20 µm, Credit to Webber et al., 2026.
Cocconeis kerguelensis, SV. LM. Scale bar: 5 µm. Photo credit to Webber et al., 2026
Neocalyptrella robusta, live, girdle view. LM. Scale bar: 50 µm, Credit to Webber et al., 2026

The findings include some curious discoveries. Several taxa are reported for the first time on the Pacific coast of North America, including Trigonium quinquelobatum, while others, such as Cocconeis kerguelensis (previously known only from the Indian Ocean) and Neocalyptrella robusta (previously confined to California), suggest a range expansion into cooler waters.

Ecologically, the genus Tabularia stands out as a dominant presence on eelgrass and macroalgae, despite having few species. In contrast, genera like Auliscus, Biddulphia, and Mastogloia are surprisingly scarce in the Salish Sea compared to other regions, leaving open questions about what limits their occurrence there.

This dataset also directly answers a key recommendation from the UN Plankton Manifesto, which urges the scientific community to strengthen plankton research and develop comprehensive plankton atlases to biomonitor the health of marine ecosystems.

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Why Diatoms? Why Now?

Bacteriastrum hyalinium — *Bacteriastrum* *hyalinium*, valve view. LM. Scale bar 20 µm. Credit to Webber et al., 2026.

The Salish Sea — the traditional territory of the Coast Salish peoples — is home to roughly nine million people and is experiencing rapid growth in urbanization, industrial activity, and marine shipping.

Because diatom populations respond quickly to changes in water quality and environmental conditions, they serve as highly effective early-warning bioindicators for shifts in ecosystem health and pollution levels.

Without a clear picture of what the base of the food web looks like today, it is impossible to understand the impact of tomorrow’s environmental changes.

Attheya longicornis — Attheya *longicornis*, girdle view. SEM. Scale bar: 10 µm. Credit to Webber et al., 2026.

“We are fortunate to have had a dedicated group of academic researchers and community scientists contribute to this work over many years,” says Mark Webber, IMERSS’ resident diatomist. “Drawing from the literature, microscope analysis, and molecular sequencing, we now have a better picture of the diatoms present in the Salish Sea. Diatoms are vital to the health of countless organisms — from shorebirds and shellfish to fish and mammals. This baseline provides a reference point for understanding changes that could ripple across the entire web of life.“

Local Research for Global Solutions

Actinoptychus adriaticus — *Actinoptychus* *adriaticus* var. *pumila*, exterior valve view. SEM. Scale bar: 5 µm. Credit to Webber et al., 2026.

The UN Plankton Manifesto stresses that understanding and managing plankton communities can unlock “Plankton-Based Solutions” to support fisheries, clean waters, and climate change mitigation.

Our work demonstrates how sustained collaboration between community scientists and research institutes can bridge these gaps, through partnering community expertise and observation with access to microscopy and molecular technologies,
the team concludes.

The new checklist and dataset will support researchers and policymakers in environmental assessments of the Salish Sea, as the team continues to refine and analyze the data to support ongoing regional research.

Original source

Webber M, Humphrey E, van Asselt A, Chang A, Morien E, Simon ADF (2026) Diatoms (Bacillariophyta) of the Salish Sea, Northeast Pacific: annotated checklist and new species reports. Biodiversity Data Journal 14: e189060. https://doi.org/10.3897/BDJ.14.e189060

About Institute for Multidisciplinary Ecological Research in the Salish Sea (IMERSS)

IMERSS, or the Institute for Multidisciplinary Ecological Research in the Salish Sea, is a non-profit society based in Galiano Island, British Columbia, Canada. IMERSS joins scientific researchers, citizen scientists, and Indigenous communities to conduct multidisciplinary ecological research, monitor biodiversity and the environment, and communicate results to better understand and respond to change in the Salish Sea bioregion.

For more interesting research, follow Biodiversity Data Journal,on Bluesky , Facebook and X.

New “Happy-Face” Spider Species Discovered in the Indian Himalayas

For over a century, this cheerful-looking creature was thought to be a unique resident of the Hawaiian Islands.

Vibrant, tiny, and sporting a bright red grin on its back, the Happy-Face spider is one of the most famous and recognisable arachnids in the world. For over a century, this cheerful-looking creature was thought to be a unique resident of the Hawaiian Islands, a biological curiosity found nowhere else on Earth.

When researchers from the Forest Research Institute and the Regional Museum of Natural History discovered a new species of spider with the same unmistakable smile in the montane mountains of Uttarakhand, India, they knew exactly what to call it: Theridion himalayana, the Himalayan Happy-Face Spider.

Mature male (left) and female (right) of *Theridion himalayana* sp. nov. Photo credit: Devi Priyadarshini and Ashirwad Tripathy.

“The discovery was accidental because our survey was [originally] on ants. But my co-author [Ashirwad Tripathy] kept sending me spiders from high altitude regions for identification.

So, one fine day, when he shared this image from the underside of a Daphniphyllum leaf, I froze in shock because I had seen the Hawaiian spider during my master’s programme itself, and I knew instantly we had a jackpot because of its striking resemblance.

I asked him to send all morphs that he found, and that led to the discovery in the next few months, from October 2023 onwards.”
Devi Priyadarshini, Regional Museum of Natural History, Bhubaneswar

Priyadarshini added that she was always interested in exploring high-altitude spiders because the landscape and vegetation are so different there than in the plains:

“This almost came across as a gateway to look at other polymorphic species from this region.”

Ashirwad also said that we could find more variations in the species if the surveys could be done extensively.

Nest architecture of *Theridion himalayana*. Photo credit: Devi Priyadarshini and Ashirwad Tripathy.

The species name, himalayana, serves as a tribute to the mountain range where the spider was found at elevations of over 2,000 meters above sea level.

“The name Himalayana was decided as the species name because we both wanted to pay our respects to the mighty Himalaya mountain ranges, which have been standing tall not just guarding our country but also holding a plethora of biodiversity within them.

Since this spider was the first polymorphic from this region, we decided to make it an ode to the amazing mountain ranges.”
Ashirwad Tripathy, Forest Research Institute, Dehradun

*Theridion himalayana* sp. nov. Photo credit: Devi Priyadarshini and Ashirwad Tripathy.

The research, published in the open-access journal Evolutionary Systematics, identified 32 different colour variations, or “morphs”, of the species collected from three locations in Uttarakhand: Makku, Tala, and Mandal. DNA analysis revealed a genetic variation of approximately 8.5% from the Hawaiian happy-face spider, confirming it as a separate lineage that evolved independently in Asia.

Different “morphs” of *Theridion himalayana* sp. nov. Photo credit: Devi Priyadarshini and Ashirwad Tripathy.

While the smiling patterns are striking, their exact purpose remains a mystery.

“The reason behind the expression of polymorphism is also very complex and unique.

These patterns definitely help them survive better in the wild, which is understood prima facie, but why do they resort to such patterns on their back, and what functional role in their life cycle does it exactly serve is yet to be deciphered. This is definitely indicative of a deeper genetic mystery.”
Priyadarshini

Ashirwad also mentioned that the spider species was surrounded by critters which had similar colour patterns on their body.

Subadult female with Psocid (booklice) prey. Photo credit: Devi Priyadarshini and Ashirwad Tripathy.

The study additionally noted that these spiders are frequently found on ginger plants (Hedychium species), mirroring the behaviour of their Hawaiian cousins. Since ginger is not native to Hawaii, the researchers are intrigued by the evolutionary connection.

“How did the spiders choose an invasive species and ginger exactly? If T. himalayana is an elder cousin of T. grallator, although discovered 125 years later!

Although this sounds like a tall claim now, it will be our further scope of work to establish any missing links, if at all, through Hedychium sps.”
Priyadarshini

Showing the prey of T. himalayana sp. nov. Video credit: Devi Priyadarshini and Ashirwad Tripathy.

Original source:

Tripathy A, Priyadarshini D (2026) On the discovery of a new polymorphic Happy-Face Spider (Araneae, Theridiidae) from the Western Himalayas, India, with notes on its natural history. Evolutionary Systematics 10(1): 63-84. https://doi.org/10.3897/evolsyst.10.174338

For more from Evolutionary Systematics, follow us on Facebook and Bluesky.

In Productive Ecosystems, Larger Animals Capture More Energy Per Species – but Human Pressure is Reshaping the Balance

A global analysis of more than 12,000 bird and mammal species reveals that ecosystems do not share energy evenly across body sizes and human activities influence this.

Guest blog post by Luis Camacho & Miguel Araújo

A global analysis of more than 12,000 bird and mammal species reveals that ecosystems do not share energy evenly across body sizes. Small species dominate in numbers, but in high-productivity regions their abundance is spread so thinly across many species that larger animals end up capturing more energy per species. Human activity compounds these patterns by selectively eroding large-bodied diversity.

How does an ecosystem distribute its energy across body sizes? A new study suggests the answer depends on where you are – and how much humans have altered the landscape. Analysing communities of birds and mammals worldwide, researchers show that larger-bodied species can, on average, capture more energy per species than smaller ones, particularly in highly productive environments. The work also reveals that human impacts restructure these patterns by disproportionately removing large-bodied species from local communities.

The research, led by Luis F. Camacho and Miguel B. Araújo is published in Frontiers of Biogeography, the journal of the International Biogeography Society.

Why body size matters for how ecosystems share energy

Workflow diagram to predict the individual density per km² of mammal and bird species across a one-degree cell grid globally. A. Global density of data points of empirical estimates of species abundance used for model training; B. Example of 80% training and 20% testing blocks used per fold in our modelling framework; C. Global maps showing the sum of predicted abundance per km² of all species across one-degree cells; D. Global estimations of species body mass-abundance relationships (MAR-SPP), individual mass distributions (IMD) and richness mass distributions (RMD). Credit to Camacho & Araújo, 2026.

Ecologists have long observed that larger species tend to have smaller populations: a bigger body requires more energy to sustain, so fewer individuals can be supported. A slope of −0.75 in the log–log relationship between body mass and abundance has been proposed as a null expectation – the point at which every species, regardless of size, commands an equal share of ecosystem energy. Yet testing this idea globally has been difficult because abundance data are patchy across regions and taxa.

This study tackles that limitation head-on. By combining large global datasets of abundance and distributions of species, the authors model local populations of birds and mammals across the planet and ask: is ecosystem energy concentrated in a few large organisms, or dispersed among many small ones – and how does that change from place to place?

What the team did

Using extensive abundance datasets and species trait information, the authors modelled population densities (individuals per km²) for 12,057 terrestrial bird and mammal species on a global grid at one-degree resolution. This enabled them to reconstruct community structure across environments and to examine three complementary signatures of how body size relates to energy and diversity within communities: the body mass–abundance relationship across species (how abundance declines with body size), the individual mass distribution (how individuals are distributed across body sizes regardless of species identity), and the richness mass distribution (how species richness is distributed across body sizes). They then related these patterns to two major global drivers: ecosystem productivity (net primary productivity) and human pressure (human footprint index).

Key findings

Relationship between species body mass and abundance (dark blue), individual mass distribution (light blue) and species-richness mass distribution (orange) in communities across one-degree cells as a function of global gradients of net primary productivity (NPP) (**A, C**) and human footprint (**B, C**). MAR-SPP, IMD and RMD slopes represent the exponent in power law relationships. Panel A shows the NPP effect on MAR-SPP, IMD and RMD values adjusted for human footprint and panel B shows the human-footprint effect adjusted for NPP. In A and B, the graph uses a boxplot format where the white central section represents the interquartile range between 25% and 75%, the central line denotes the median and the shaded areas indicate the whiskers. Outliers are omitted for clarity. The dashed line depicts a reference of slope = -0.75. Boxplots were calculated in intervals of 0.001 for NPP and every unit of human footprint raised to the 1/4 power. Lines were smoothed with a loess regression with a 0.06 span (α). The boxplots were drawn from the mean value per one-degree cell across 10 global datasets. In A and B, thicker lines represent the mean slopes of 10,000 general linear model (GLM) iterations (1000 iterations on 10 data sets), based on random samples of 20 one-degree cells. In C, GLM slopes are shown across the combined effects of NPP and human footprint. GLM slopes (thick lines in A and B and coloured areas in C) appear to depict non-linear relationships because of back-transformation of NPP and human footprint, which were squared-root and fourth-root transformed for GLM. Credit to

1. Productive ecosystems tilt energy capture towards larger species.

As productivity increases, the study finds that small-bodied species become more diverse without a matching rise in total abundance. Individuals are effectively “spread thinner” across more small-bodied species, reducing the average energy share per small-bodied species. Meanwhile, large-bodied species – fewer in number but less diluted by richness – end up capturing more energy on average. The body mass-abundance slope ranged from approximately −0.69 in the least productive environments to −0.35 in the most productive, consistently shallower than the −0.75 null expectation.

2. Human pressure reshapes community organisation, with lasting consequences.

Human activity produces a shift in these relationships that resembles – but is mechanistically distinct from – the productivity effect. Human impact operates primarily by reducing both the abundance and, more strongly, the species richness of large organisms. This likely reflects the well-documented disproportionate extirpation of large-bodied species by human activities, leaving a persistent imprint on how energy and diversity are distributed across body sizes.

3. Energy distribution and ecological opportunity vary independently.

Across the globe, patterns of energy flow across body sizes and the opportunities for diversification (how many species exist at each body size) can decouple. Interestingly, the distribution of species richness across body sizes was more stable across environments than the distribution of energy – yet it had a stronger influence on the body mass–abundance relationship. This helps explain why simple, one-size-fits-all expectations about body size and abundance often fail at large scales.

Why it matters

The authors argue that body mass–abundance–richness relationships can serve as a functional metric of ecological change – capturing not just how many species are present, but how ecosystems allocate individuals and energy across body sizes. This matters for biodiversity assessments because losing large-bodied diversity can reorganise ecosystems in ways that species counts alone cannot reveal. Specifically, these patterns may help improve biodiversity offset strategies and address the risk of underestimating the ecological importance of large-bodied species.

Small-bodied animals still dominate numerically, but in productive ecosystems they are divided among many more species. That dilution changes the per-species share of individuals and, by extension, energy.
Luis F. Camacho, first author

Human pressure does not just remove species; it reshapes the functional organisation of communities. Looking at body size, abundance, and richness together reveals structural changes that standard indicators miss.
Miguel B. Araújo, senior author

Original source:

Camacho LF, Araújo MB (2026) Body mass–abundance relationships reveal uneven global energy distribution across body size classes in vertebrates. Frontiers of Biogeography 19: e164408. https://doi.org/10.21425/fob.19.164408

Tiny Hitchhikers in a Big World: How pseudoscorpions travel on flies

A new study published in ZooKeys offers the most comprehensive synthesis of pseudoscorpion–Diptera phoresy, including new European records.

Guest Blog Post by Dr. Jana Christophoryová

Imagine living in a world where your home can disappear overnight.

For many tiny arthropods, such as pseudoscorpions, this is a reality. They inhabit ephemeral and unpredictable habitats – decaying organic matter, animal nests, or tree hollows – that can quickly vanish or become unsuitable. Without wings, escaping these disappearing habitats poses a serious challenge.

So how do they cope?

The answer lies in a fascinating strategy known as phoresy: hitchhiking on other, more mobile organisms. In the case of pseudoscorpions, these carriers are often flies.

Flies (Diptera) are particularly suitable transport hosts. They are highly mobile, capable of long-distance flight, and frequently visit the same types of transient habitats that pseudoscorpions depend on. By attaching themselves to a fly, pseudoscorpions can effectively outsource dispersal – reaching new habitats they could never access on their own.

Despite its importance, the relationship between pseudoscorpions and flies has remained largely underexplored. Comprehensive syntheses are more than two decades old, and much of the available knowledge has been scattered across individual studies, often published in different languages and difficult to access.

What began as a marginal aspect of our research gradually turned into a much greater effort. As we followed scattered records across the literature, it became clear that no up-to-date overview existed. This led us to examine hundreds of publications from different countries and time periods, critically reassessing old records while adding new data from our own material.

Altogether, we compiled 172 records spanning more than 250 years, from 1761 to 2025 – providing the most comprehensive overview of pseudoscorpion – Diptera phoresy to date now published in the open-access journal ZooKeys.

New records of pseudoscorpion phoresy in Europe. Locality codes are given in Materials and methods. Country abbreviations: CZ – Czechia, FR – France, SI – Slovenia, SK – Slovakia. Image credit: Jana Christophoryová et al.

Our results show that pseudoscorpions have been recorded hitchhiking on at least 74 species of flies across 30 families, while the number of known pseudoscorpion travellers reaches 39 species from seven families. Several new host associations were identified, including seven fly species and three fly families not previously known to serve as carriers. We also documented 11 new cases of phoresy from Europe, including first national records for some species.

Cases of phoresy from Czechia, Slovakia, and Slovenia. A. *Ceroxys* *urticae* and *Lamprochernes* cf. *chyzeri* (locality 1); B. *Pherbellia* *annulipes* and *Pselaphochernes* *scorpioides* (locality 6); C. *Fannia* *canicularis* and P. *scorpioides* (locality 7); D. *Xylophagus* *ater* and *Chernes* *cimicoides* (locality 8); E. *Musca* *autumnalis* and L. cf. *chyzeri* (locality 9); F. *Lonchaea* *chorea* and L. cf. *chyzeri* (locality 10); G, H. *Limonia* *nubeculosa* and P. *scorpioides* (locality 11). Image credit: Jana Christophoryová et al.

Interestingly, most records are linked to a single, familiar species – the house fly (Musca domestica). However, this pattern is likely influenced by historical research bias, as earlier studies focused heavily on this easily observable association. This highlights an important challenge: understanding phoresy requires not only new data, but also careful re-evaluation of past identifications.

Beyond modern observations, fossil evidence preserved in amber reveals that these interactions are far from recent. Pseudoscorpions were already hitchhiking on flies tens of millions of years ago, indicating that this dispersal strategy has deep evolutionary roots.

Cases of phoresy from France. A, B. *Scatopse* *notata* and *Pselaphochernes* *scorpioides* (locality 2); C, D. *Physiphora* sp. and *Lamprochernes* *nodosus* (locality 3); E, F. *Neolimonia* *dumetorum* and P. *scorpioides* (locality 4); G, H. *Tipula* *vernalis* and *Dactylochelifer* *degeerii* (locality 5). Image credit: Jana Christophoryová et al.

Taken together, our findings show that phoresy is not just an occasional curiosity, but a widespread and long-standing ecological strategy. It allows these tiny, wingless predators to navigate a fragmented and ever-changing world – by quite literally catching a ride.

Original source:

Christophoryová J, Mathy V, Hörweg C, Vičanová L (2026) Hitchhiking across continents: phoresy of pseudoscorpions (Arachnida, Pseudoscorpiones) on Diptera, with new European records. ZooKeys 1276: 213-248. https://doi.org/10.3897/zookeys.1276.188186

For more articles on zoology, visit the ZooKeys website and follow the journal on BlueSky and Facebook.

Celebrating Deep Day with Incredible Deep-Sea Research

Protecting the deep sea, the largest and least explored habitat on Earth, requires collaborative effort.

May 7th marks Deep Day, a global day of awareness and action dedicated to the deep sea. Founded by the Deep Sea Conservation Coalition, it aims to raise awareness of the deep sea’s immense ecological importance and call for its protection against threats like deep-sea mining and destructive fishing.

To celebrate the wonders of our oceans and raise awareness of the incredible biodiversity of the deep sea, we at Pensoft Publishers would like to highlight some of the remarkable marine studies that have recently been published in our scientific journals.

A Global Collaboration to Uncover Deep-Sea Amphipods

24 deep-sea amphipods — The 24 newly described deep-sea amphipod species. Image credit to: Eleanor Frost, National Oceanography Centre

Demonstrating the power of global teamwork, an international group of experts recently discovered 24 new deep-sea amphipod species in the central Pacific Ocean’s Clarion-Clipperton Zone (CCZ). Researchers from institutions worldwide, including the University of Lodz and the National Oceanography Centre, came together for a coordinated taxonomy workshop to achieve this. Their work revealed a completely new evolutionary branch with the discovery of a new superfamily, Mirabestioidea.

Crucially, their findings form part of the International Seabed Authority’s Sustainable Seabed Knowledge Initiative (SSKI) and its ‘One Thousand Reasons’ project, which aims to formally describe 1,000 new species by the end of the decade.

Highlighting the importance of this joint effort, Dr. Anna Jażdżewska from the University of Lodz shared:

This was a truly collaborative process that allowed us to achieve the ambitious goal of describing more than 20 species new to science within a year – something that would not have been possible if each of us worked independently. The team’s findings provide information that is crucial for future conservation and policy decisions.

Learn more in the Special Issue: New deep-sea Amphipoda from Clarion-Clipperton Zone

What lives 10 km below the surface?

@pensoft.publishers
😯Fascinating new #study recorded 108 morphotaxa from 4,500m down to the #hadal depths of 9,775m, revealing the hidden life of the NW Pacific trenches. 🎥They analyzed 460 hours of video from landers & submersibles across the Japan, Ryukyu, and Izu-Ogasawara trenches. 👇Full study here: https://doi.org/10.3897 /BDJ.14.e182172 📗You can read all about it on Pensoft’s blog 👇 https://blog-pensoft.blogs.awt-2.arphahub.com/2026/04/06/what-lives-10-km-below-the-surface-a-new-look-at-life-in-japans-deepest-ocean-trenches/ Research center: Minderoo-UWA Deep-Sea Research Centre. Main funders of the expedition: Inkfish, Caladan Oceanic #deepsea #sciencetok #research
♬ THE MOON – Camargguinho

Photo and video credit to Minderoo-UWA Deep-Sea Research Centre, Inkfish, Caladan Oceanic, Jamieson et al., 2026

Another recent expedition provided a profound look at life up to nearly 10 kilometers below the surface in the Japan, Ryukyu, and Izu-Ogasawara trenches, cataloging at least 108 distinct organism groups. The research captured rare footage of species interactions at extreme depths – and one baffling, unidentified animal that has left taxonomists worldwide perplexed.

The unknown organism or Animalia incerta sedis. Credit to Jamieson et al., 2026, o Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.

Rather than using traditional trawls that can damage fragile organisms, the team utilized crewed submersibles and free-fall baited landers. Explaining the value of this non-destructive method, the research team noted:

This combination enabled us to build the most comprehensive visual baseline yet for abyssal and hadal megafauna in the Northwest Pacific to date.

They added that the study aims to establish a foundation for the future, emphasizing that:

More than anything, the hadal zone remains one of Earth’s least-explored and most intriguing frontiers.

Learn more: Jamieson AJ, Swanborn DJB, Bond T, Cundy MC, Fujiwara Y, Lindsay D, Stott MS, Kitazato H (2026) Faunal biodiversity of the lower abyssal and hadal zones of the Japan, Ryukyu and Izu-Ogasawara trenches (NW Pacific Ocean; 4534-9775 m). Biodiversity Data Journal 14: e182172. https://doi.org/10.3897/BDJ.14.e182172

The Internet Names a New Deep-Sea Chiton

Finally, highlighting a unique way the public can engage with science and taxonomy, a recently found deep-sea chiton was named by the internet after science YouTuber Ze Frank featured it in an episode of his “True Facts” series. Originally discovered in 2024 within the Izu-Ogasawara Trench at a depth of 5,500 meters, this new species belongs to the genus Ferreiraella, a rare and specialized group of mollusks that live exclusively on sunken wood in the deep sea.

From over 8,000 suggestions submitted across social media, the research team selected the name Ferreiraella populi. The epithet populi is a Latin singular noun in the genitive case meaning “of the people”.

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Prof. Dr. Julia Sigwart, co-chair of the Senckenberg Ocean Species Alliance (SOSA), emphasized the broader significance of this public discovery:

Ferreiraella populi exemplifies the overwhelming biodiversity of the oceans, the vast majority of which remains unexplored. Many species go extinct before we even know they exist – this is especially true for marine invertebrates.

Learn more: (SOSA) SOSA, Chen C, Frank H, Kraniotis L, Nakadera Y, Schwabe E, Sigwart JD, Trautwein B, Vončina K (2026) Ocean Species Discoveries 28–30 — new species of chitons (Mollusca, Polyplacophora) and a public naming competition. Biodiversity Data Journal 14: e180491. https://doi.org/10.3897/BDJ.14.e180491

@pensoft.publishers
Happy #DeepDay ! Started by Deep Sea Conservation Coalition, this annual day is aimed at raising awareness to the incredible diversity in our deep seas. Today, we’re sharing with you three remarkable studies from our journals – each one a window into a fascinating world, hoping to raise awareness and inspire action to #DefendtheDeep . 👇𝐎𝐮𝐫 𝐛𝐥𝐨𝐠: https://blog-pensoft.blogs.awt-2.arphahub.com/…/celebrating-deep-day-with…/ 🔎By analysing 460 hours of video from landers and submersibles across the Japan, Ryukyu, and Izu-Ogasawara trenches, researchers found something extraordinary: a mysterious organism so unusual it was classified as Animalia incerta sedis! 📗𝐑𝐞𝐚𝐝 𝐭𝐡𝐞 𝐟𝐮𝐥𝐥 𝐬𝐭𝐮𝐝𝐲 𝐩𝐮𝐛𝐥𝐢𝐬𝐡𝐞𝐝 𝐢𝐧 Biodiversity Data Journal (𝐁𝐃𝐉) 𝐡𝐞𝐫𝐞: https://doi.org/10.3897/BDJ.14.e182172 Cc: Minderoo-UWA Deep-Sea Research Centre at The The University of Western Australia, JAMSTEC: Japan Agency for Marine-Earth Science and Technology, Inkfish, Caladan Oceanic LLC 🎥Footage credit: Minderoo-UWA Deep-Sea Research Centre, Inkfish, Caladan Oceanic, Jamieson et al., 2026 After thousands of name suggestions from the public, the “chiton of the people” has been officially described in Biodiversity Data Journal. 🙌A huge thank you to everyone who voted and participated! Cc: True Facts Senckenberg Senckenberg Ocean Species Alliance – SOSA 🎥Footage credit: ©ChongChen/JAMSTEC 𝐅𝐮𝐥𝐥 𝐚𝐫𝐭𝐢𝐜𝐥𝐞 𝐢𝐧 𝐁𝐃𝐉: https://doi.org/10.3897/BDJ.14.e180491 🦐24 new deep-sea amphipods discovered in the Clarion Clipperton Zone. Through an international collaboration – with key momentum from a 2024 taxonomic workshop at Uniwersytet Łódzki – researchers described 24 new species of amphipods from the central Pacific abyss. 𝐀𝐜𝐜𝐞𝐬𝐬 𝐚𝐥𝐥 𝐭𝐡𝐞 𝐩𝐮𝐛𝐥𝐢𝐜𝐚𝐭𝐢𝐨𝐧𝐬 𝐢𝐧 ZooKeys: https://zookeys.pensoft.net/issue/4856/ See less #deepsea #deepocean #sciencetok
♬ Fantasy in an Immersive World – Ernesto P. Neto

These studies highlight the vastness of the unexplored frontier that our deep seas and oceans offer. Revealing this hidden life – from entirely new evolutionary branches of amphipods to records of unknown organisms – requires global collaboration, cutting-edge exploration technologies, and the involvement of the general public.

Ultimately, this shared pursuit of discovery provides the fundamental knowledge crucial for conservation and policy decisions. As Deep Day reminds us of the encroaching threats from deep-sea mining, human-derived debris, and destructive fishing, we must work together to understand these fragile habitats so that we can effectively protect them and #DefendtheDeep.

For more curious research follow Pensoft Publishers’ socials: Facebook, Bluesky, Instagram, TikTok, LinkedIn and X.

New ‘Ecclesiastical’ Moth named after Pope Leo XIV

Described as Pyralis papaleonei, the finding serves as a powerful call for biodiversity conservation, inspired by a biblical reference.

Distinguished by its striking colors and a name that carries the weight of a high ecclesiastical office, a new species of moth has been discovered in the rugged terrain of Greece. When researchers from the Tyrolean State Museum, the Finnish Museum of Natural History and the Bavarian State Collection of Zoology identified this unique insect in the White Mountains of Crete, they chose a name that reflects both its noble appearance and a message of environmental hope: Pyralis papaleonei – derived from “Papa Leone” (Pope Leo).

The discovery, published in the open-access journal Nota Lepidopterologica on 28 April 2026, highlights that even among such conspicuous European moths, overlooked species remain to be discovered. The new species is currently only known from the White Mountains (Lefka Ori) in the western part of Crete, where it appears to be an endemic treasure of the island.

Type-locality of *Pyralis papaleonei* sp. nov. (Greece, Crete, Omalos plateau). Image credit: Peter Huemer.

Striking purple forewings

The so-called Pope Leo Moth has a wingspan of around two centimeters, placing it among the medium-sized representatives of its group. Its most distinctive features are its purple forewings with an orange-golden patch and prominent white bands. The moths were recorded at artificial light sources and appear to be mainly active in June. So far, little is known about the biology and lifestyle of the new species. It was distinguished from related species based on classical morphological characteristics – such as wing pattern, coloration, and genital morphology – as well as genetic fingerprinting. Molecular analyses revealed a divergence of around six percent from its closest relative, clearly indicating that it represents a distinct species.

*Pyralis papaleonei* sp. nov., holotype. Image credit: Peter Huemer.

A tradition of remarkable species names

Butterflies and moths are often named after physical characteristics, geographic origins, or in honor of distinguished individuals. Within the genus Pyralis, however, a particular tradition can be observed: as early as 1775, Austrian naturalists Michael Denis and Ignaz Schiffermüller described the first species of the group as Pyralis regalis (“royal”), inspired by its splendid coloration. This was followed by sonorous names such as Pyralis princeps and Pyralis cardinalis, also referring to the remarkable beauty of these moths.

All these species belong to the diverse superfamily Pyraloidea, which comprises around 16,000 described species worldwide and represents one of the largest groups among micro-moths.

Specimen of *Pyralis regalis.* Image credit: Peter Huemer.

Taxonomy as the “first profession” of humankind

The naming of living organisms also has a cultural-historical dimension: in the Old Testament (Genesis 2), Adam is firstly tasked with naming all animals. In this sense, taxonomy – the science of classifying, naming, and organising organisms – can be regarded as one of humanity’s earliest endeavors.

For study leader Peter Huemer of the Tyrolean State Museum Ferdinandeum, naming a species is therefore more than a formal scientific act: it also serves as a symbolic appeal to the head of the Catholic Church, Pope Leo XIV, to highlight humanity’s central responsibility in safeguarding creation. This is particularly fitting as butterflies and moths are regarded in Christianity as symbols of resurrection, transformation (metamorphosis), and the immortal soul.

Specimens of *Pyralis papaleonei.* Image credit: Peter Huemer.

Only a fraction of global biodiversity documented

Peter Huemer, former head of the Natural Science Collections at the Tyrolean State Museums and now a volunteer researcher, explains:

“We are facing a global biodiversity crisis, yet only a fraction of the world’s species has been scientifically documented. Effective conservation of biodiversity requires that species are first recognised, described, and named.”

Around 700 new moth species are described each year, primarily in the tropics. However, fundamental research in Europe is far from complete: in the Alps alone, approximately 200 previously unknown species have been identified in recent decades.

With their internationally significant scientific collections, the Tyrolean State Museums make an important contribution to this work. The discovery of the Pope Leo Moth, Pyralis papaleonei, highlights how much remains to be discovered even in well-studied regions of Europe—and underscores the urgent need to protect sensitive habitats.

Original source:

Huemer P, Kaila L, Segerer AH (2026) Pyralis papaleonei sp. nov. from Crete (Greece) (Lepidoptera, Pyralidae). Nota Lepidopterologica 49: 63-74. https://doi.org/10.3897/nl.49.185483

For more interesting articles on lepidopterology, follow Nota Lepidopterologica on Bluesky and Facebook.

A Simple Filter Swap Could Advance Marine eDNA Biomonitoring

A simple adjustment to water filtration methods can dramatically improve the detection of marine animal DNA when using advanced, PCR-free sequencing.

Over the past two decades, environmental DNA (eDNA) analysis has become a crucial tool for monitoring aquatic ecosystems. The most common method, metabarcoding, relies on PCR amplification of a smaller genetic region to identify specific taxa. However, PCR can lead to “significant taxonomic bias” because it often amplifies the DNA of different organisms unequally, making quantitative estimates difficult.

To avoid this, scientists have increasingly explored “shotgun sequencing“- an approach that sequences the DNA in a sample much more broadly – across the entire tree of life and across the genome. Unfortunately, in marine environments, shotgun sequencing is typically overwhelmed by microbial DNA, burying the genetic traces of less abundant macro-organisms such as animals.

Bigger Pores, Better Animal DNA Capture?

In a new study published in Metabarcoding and Metagenomics, researchers investigated if they could capture a higher proportion of eukaryotic (animal and plant) DNA simply by using filters with larger pore sizes.

Filter pore sizes are expected to influence results, since eDNA may be present in many different states, including but not limited to complete organisms, sloughed tissue, feces, free DNA, or gametes.
commented Dr. Adrián Gómez-Repollés, the lead author of the study.

To test this, the team collected 15 seawater samples from Skovshoved Harbour in Denmark and filtered them using pore sizes ranging from 0.2 µm to 8.0 µm. The results showed a stark contrast in the type of DNA captured based on the filter size.

Filters with smaller pore sizes (0.2 µm and 1.2 µm) retained a significantly greater proportion of bacterial reads than eukaryotic reads (63% vs. 28%); conversely, filters with larger pore sizes (5.0 µm and 8.0 µm) retained a significantly greater proportion of eukaryotic reads than bacterial reads (49% vs. 31%).

By switching to 5.0 µm or 8.0 µm filters, the researchers successfully reduced the dominance of bacteria. Of the 19 metazoan (animal) phyla detected using shotgun sequencing, all but one were found to be more abundant when using the larger pore sizes.

Looking to the Future of Biomonitoring

Taxonomic comparison at the kingdom and phylum levels of eukaryotes detected with shotgun sequencing and metabarcoding. A. Number and relative abundance (percentages) of taxonomically classified reads after rarefaction per sample and kingdom for shotgun sequencing; B. Number and relative abundance of taxonomically classified reads after rarefaction per sample and kingdom for metabarcoding. For both heatmaps, sample replicates are ordered along the y-axis by increasing pore size, starting with the enclosed filter type (EN) and continuing with the open pore filter type (OP). Pore sizes are in µm; C. Cladogram of the full set of eukaryotic phyla identified by shotgun sequencing and metabarcoding. Branch colors represent kingdoms (blue, Metazoa; red, Fungi; green, Viridiplantae; pink, other eukaryotes). Three surrounding rings indicate phyla shared between shotgun sequencing and metabarcoding (gray), phyla uniquely detected with metabarcoding (yellow), and phyla uniquely detected with shotgun sequencing (blue). Information in the rings is summarized in a Venn diagram in the upper left corner. Taxa marked with an asterisk are no longer categorized as a phylum. Credit to Gómez-Repollés et al., 2026

When compared alongside traditional 18S rDNA metabarcoding, the shotgun sequencing method successfully shared 39 of the 54 detected eukaryotic phyla, indicating a similar performance in detecting the presence of high-level taxonomic groups.

To test the potential of shotgun sequencing in applied biomonitoring even further, the researchers examined the results at genus-level for a number of well known marine animals such as fish, mussels, crustaceans and bristle worms. Here, they found both DNA matches to native Danish species but also to exotic taxa that were highly unlikely and probably due to the low level of resolution in shotgun sequencing, where genetic regions of low variation and coverage are sequenced.

Water sample collection. Photo by David Stanciu.

But, when they looked further into the results they observed that the local taxa consistently comprised a higher number of reads. The number of reads could thus be a simple way to initially separate authentic taxa from erroneous matches in eDNA studies based on shotgun sequencing, although the approach needs further testing.

However, the authors note current limitations with the technology, primarily driven by incomplete public DNA reference databases. In the study, only 0.78% of the total shotgun reads could be definitively assigned to a superkingdom level. Another drawback was the lack of field controls to rule out cross-contamination or input from airborne DNA, coupled with a limited spatiotemporal design involving only a single sampling location.

Despite these hurdles, shotgun sequencing and filters with larger pore sizes could potentially be a significant step forward for eDNA in marine biology. As global genomic databases continue to expand, “the taxonomic coverage and resolution of shotgun sequencing should improve, likely enhancing the potential of shotgun sequencing for future eDNA research“, says Philip Francis Thomsen, professor and senior author on the study.

Original study:

Gómez-Repollés A, Sigsgaard EE, Jensen MR, Thomsen PF (2026) Filter pore size influences taxonomic composition of retained eDNA from seawater samples—evidence from shotgun sequencing. Metabarcoding and Metagenomics 10: e164232. https://doi.org/10.3897/mbmg.10.164232

The Evolutionary Adaptations of Cave-Dwelling Catfish in Brazil

What do brain morphology and sensory structures tell us about the evolutionary adaptations between catfish that live on the surface and those that live in caves?

Cave fauna fascinates young and old alike. Deep within the karst systems of Chapada Diamantina, Brazil, lives one of the world’s most diverse groups of cave-dwelling fish.

In fact, Brazilian cavefishes are the richest troglobitic (cave-dwelling) ichthyofauna worldwide, boasting 13 different genera. While the surface world is teeming with life, the subterranean realm, or the hypogean habitat, demands a very specific set of skills to survive.

The research, conducted by Thalia Rodovanski (from the Departamento de Biologia, Universidade Federal de São Carlos, Brazil) and her team, was published in Subterranean Biology and took a closer look at the Copionodontinae, a subfamily of primitive catfishes.

Shallow water pool in Igatu. Photo credit to Maria Elina Bichuette.

Building on previous findings regarding the aggressive (agonistic) nature of Copionodontinae species, the researchers used this behavioral foundation to investigate how their physical and sensory structures have evolved in response to their environment.

By comparing surface-dwelling (epigean) species such as Copionodon pecten, C. lianae, and G. rodriguesi with their cave-bound cousin, Glaphyropoma spinosum, the researchers undertook the task of uncovering how these fish transitioned from the sunlit rivers to the pitch-black cave riverine systems.

Specifically, they did this by measuring the brain morphology and sensory structures such as barbels, eyes and counted pores of the lateral canal system on the head.

Shallow water pools in Igatu. Photo credit to Maria Elina Bichuette.
Researcher in a cave system in Igatu. Photo credit to Maria Elina Bichuette.

The curious findings

One of the most striking finds involved the genus Glaphyropoma. While the cave-dwelling G. spinosum shows classic troglomorphisms (adaptations for life in constant darkness), such as reduced eyes and a loss of skin pigment, the researchers found something surprising: even the surface-dwelling species in this group showed eye asymmetry and reduction.

*Copionodon pecten*. Photo credit to Maria Elina Bichuette.

Based on this, the researchers hypothesized that the asymmetry in the eyes is a plesiomorphic character (an ancestral trait) of the genus, rather than a feature developed in response to the specific habitat of each species. This pre-existing condition likely favored the colonization of hypogean (underground) habitats by G. spinosum.

In other words, Glaphyropoma already had a tendency toward reduced eyes. Instead of evolving small eyes because of the cave environment, they likely had them from the start. This is known as exaptation: a trait that originally evolved for one function (or no function at all) and was later co-opted for a new, different purpose, in this case, better suited for the dark.

*Glaphyropoma spinosum*. Photo credit to Adriano Gambarini.

As you can imagine, seeing in pitch black is quite hard. Therefore, these species had to rely on their other senses. The study found that the cave-dwelling G. spinosum has a longer telencephalon than its relatives. This is significant because it is the part of the brain responsible for navigating through chemical cues, creating mental maps (spatial memory), and participating in social interactions. Interestingly, the mesencephalon (the vision-processing center) hasn’t shrunk significantly yet, suggesting that these fish are still in the middle of their evolutionary transition.

The researchers concluded that while G. spinosum shows clear cave-specialized traits, many of these features are shared by its surface-dwelling cousins.

However, because of a lack of specimens of G. rodriguesi, the only known epigean species of the genus, which occurs sporadically in caves, it is not yet possible to definitively conclude if the sensory troglomorphisms detected in this study are related to taxonomic identity or the habitat itself.

Ultimately, such research is key to understanding more about the complex life of the highly specialized species that inhabit these fascinating environments.

Original source:

Rodovanski T, Bichuette ME, Cetra M, Mattox GMT (2026) The influence of subterranean habitats in the sensorial and brain morphology of hypogean and epigean Copionodontinae catfish (Siluriformes, Trichomycteridae). Subterranean Biology 55: 27-42. https://doi.org/10.3897/subtbiol.55.175751

A New Species of Fly Found on the Lesser Brown Horseshoe Bat

A bizarre new species of parasitic fly sheds its wings and legs to live permanently embedded in a bat’s ear.

Imagine a fly that decides flying is overrated. Instead, it finds a bat, sheds its wings, drops its legs, and burrows into the host’s skin for the rest of its days. This is the reality of the genus Ascodipteron, a group of highly specialised bat flies that challenge our basic definition of what an insect looks like.

In a recent study published in the open-access journal ZooKeys, researchers led by Haoran Sun of Beijing Forestry University have identified a new member of this strange family in the Yunnan Province of China. It brings some fascinating, if slightly macabre, biological quirks to the table.

The newly discovered species has been named Ascodipteron euryale and was found on the lesser brown horseshoe bat, known scientifically as Rhinolophus stheno. This discovery is particularly significant because it represents the first time a fly from this genus has been documented on this specific species of bat. These flies often show an incredibly narrow host range and a strict preference for where they live on the bat’s body. In the case of Ascodipteron euryale, they prefer the base of the bat’s ear, the tragus, or the ear pinna.

*Ascodipteron* *euryale* sp. nov. and its host *Rhinolophus* *stheno*. (Image credit: Haoran Sun et al.).

The life of a female Ascodipteron fly is especially interesting. After a very brief period of seeking out a host, the female undergoes a radical transformation into what scientists call a neosome. It essentially becomes an endoparasite, embedded so deeply in the bat’s tissue that often only its posterior end is visible, protruding slightly so it can breathe and release larvae. This particular species was discovered in Xianren Cave, located in the Simao District of Pu’er City, at an elevation of 2428 meters above sea level.

*Ascodipteron* *euryale* sp. nov., ex. R. *stheno* – the top two images display the whole neosome. (Image credit: Haoran Sun et al.).

What makes Ascodipteron euryale stand out from its 17 known cousins? The most defining physical trait is the shape of its mesosternum, a part of its underside, which features gently rounded lobes on the back corners. Further, unlike many related flies that are covered in soft skin and easily removed, these neosomes were found encased in a fibrous cyst or shell – this is a reaction from the host bat’s own immune system, creating a protective barrier that makes the parasite very difficult to extract.

*Ascodipteron* *euryale* sp. nov., ex. R. *stheno*, head and thorax. (Image credit: Haoran Sun et al.).

The naming of the species is a clever nod to Greek mythology. The host bat, Rhinolophus stheno, shares a name with Stheno, one of the three Gorgon sisters who could turn onlookers to stone. The researchers decided to name the new fly euryale after Euryale, another of the Gorgon sisters. In the myths, these two sisters were immortal, and the authors note that this name choice reflects their hope that the deep-rooted biological association between this specific bat and its resident fly continues long into the future.

This research adds a sixth species of Ascodipteron to the records in China, emphasising the impressive biodiversity hidden within the country’s cave systems. It also raises new questions for future study, particularly regarding why some of these flies trigger the formation of fibrous shells while others do not. For now, Ascodipteron euryale remains a testament to the strange and highly specific ways life finds a niche (even if that niche is the inside of a bat’s ear)!

Original source:

Sun H, Ding L, Zhang D, Pape T (2026) Ascodipteron (Diptera, Nycteribiidae, streblid grade) from China: a new species from the lesser brown horseshoe bat, Rhinolophus stheno. ZooKeys 1273: 277-286. https://doi.org/10.3897/zookeys.1273.183551