Year of the Horse 2026: A selection of equine-related species to celebrate the Lunar New Year

Pensoft celebrates the Year of the Horse by showcasing scientific discoveries of equine-adjacent species.

Lunar New Year is a celebration of the arrival of spring and the beginning of a new year on the lunar calendar. As the most important holiday in China, it is also widely celebrated across Korea, Vietnam, and other countries with a substantial Chinese diaspora.

In celebration of 2026 as the Year of the Horse, we reviewed our journals for horse-related studies. While our recent publications do not focus on horses themselves, we have highlighted several fascinating species that share an equine connection in their names.

2026 may be the Year of the Fire Horse, but we start our series with a creature of the opposite element: the seahorse!

Hippocampus japapigu in situ, Hejie, Kenting, Taiwan. (Photo credit: Chao-Tsung Chen).

Monitoring tiny, cryptic pygmy seahorses can be costly and logistically challenging. To overcome this, researchers from Taiwan turned to citizen science, gathering photographs from divers and underwater photographers via social media. Five species were identified, including two never before recorded in the region.

Among them is the charismatic “Japan pig” seahorse, Hippocampus japapigu, originally described from Japan in the open-access journal ZooKeys.

At the time, only seven pygmy seahorses had been identified globally. Documenting five of them in Taiwan established the region among the world’s biodiversity hotspots for these miniature fish.

Read more: ZooKeys 883: 83–90. https://doi.org/10.3897/zookeys.883.39662

But seven did not remain the final count for long. In Chinese tradition, eight is considered an auspicious number, associated with prosperity and good fortune.

Enter Hippocampus nalu – the eighth recognized pygmy seahorse species!

Hippocampus nalu in situ, Sodwana Bay, South Africa at 14 m depth. (Photo credit: Richard Smith, oceanrealmimages.com).

It is also the first confirmed true pygmy seahorse recorded from Africa. Measuring just 20 mm, this tiny species was discovered at depths of 17 m on a sandy coral reef in Sodwana Bay, South Africa.

Read more: ZooKeys 934: 141–156. https://doi.org/10.3897/zookeys.934.50924

Seahorses also feature in a remarkable Mediterranean story…

A study published in Acta Ichthyologica et Piscatoria documented a stable and conspicuous population of the long-snouted seahorse, Hippocampus guttulatus, in a highly polluted coastal lagoon in the Ionian Sea.

Hippocampus guttulatus observed during the diving visual census carried out in the Mar
Piccolo of Taranto (Ionian Sea), 2011-2013. (Photo credit: Francesco Tiralongo and Rossella Baldacconi).

Through three years of diving surveys, amounting to 69 hours underwater, researchers recorded 196 sightings. The seahorses showed a clear preference for artificial hard substrates, while only a few individuals were found in algal meadows. 

Despite environmental fluctuations and pollution, the population persists. In the Year of the Horse, we wish you the same resilience and strength!

Read more: Acta Ichthyologica et Piscatoria 44(2): 99–104. https://doi.org/10.3750/AIP2014.44.2.02

Fish is a traditional Lunar New Year dish, symbolising abundance and good fortune. While you won’t find a horsefish at the markets of Hainan, China, you can certainly spot a ponyfish.

Researchers have reported the first confirmed record of Aurigequula striata in Chinese waters, based on specimens collected at a fish market in Sanya, Hainan Island.

Aurigequula striata, left lateral view. (Photo credit: Jia-Jie Chen).

Live seafood markets have long proven to be unexpected hotspots for scientific discovery – just like the remarkable giant isopod Bathynomus vaderi described from market-purchased material in Vietnam.

As fresh as the seafood on display, this discovery was published in late January 2026 in ZooKeys. Newly collected specimens of Aurigequula fasciata enabled detailed morphological and genomic analyses, including the first complete mitochondrial genomes for both species and new phylogenetic insights into the family Leiognathidae.

Aurigequula fasciata, left lateral view. (Photo credit: Jia-Jie Chen).

Read more: ZooKeys 1267: 31–49. https://doi.org/10.3897/zookeys.1267.174380

Fittingly, we close with a horseshoe bat once feared lost. Its name bridges our equine theme with a traditional Chinese symbol: the word for bat (fú, 蝠) is a homophone for blessing (fú, 福), representing happiness and prosperity.

Hill’s horseshoe bat (Rhinolophus hilli), listed as Critically Endangered and unseen since 1981, was rediscovered in Nyungwe National Park, Rwanda, after 40 years.

Rhinolophus hilli, first observation of this species since 1981 in Nyungwe National Park. (Photo credit: Flanders, et al.).

Through cave surveys, forest capture efforts, and long-term acoustic monitoring, researchers confirmed the survival of this elusive species, bringing renewed hope for its conservation. 

Read more: Biodiversity Data Journal 10: e83546 https://doi.org/10.3897/BDJ.10.e83546

As we gallop into 2026, may the Year of the Horse bring you strength, endurance, and a stable path toward success. On behalf of Pensoft, we wish you a happy, healthy and prosperous New Year!

Original sources:

Chen J-J, Zhong J-S, Zeng S, Yang D-Y, Liu P, Wang X-D, Zhang H-Y, Ye J-Q (2026) A new leiognathid record from China with complete mitogenomes and phylogenetic insights of two Aurigequula (Teleostei, Leiognathidae) species. ZooKeys 1267: 31-49. https://doi.org/10.3897/zookeys.1267.174380

Flanders J, Frick WF, Nziza J, Nsengimana O, Kaleme P, Dusabe MC, Ndikubwimana I, Twizeyimana I, Kibiwot S, Ntihemuka P, Cheng TL, Muvunyi R, Webala P (2022) Rediscovery of the critically endangered Hill`s horseshoe bat (Rhinolophus hilli) and other new records of bat species in Rwanda. Biodiversity Data Journal 10: e83546. https://doi.org/10.3897/BDJ.10.e83546

Heard J, Chen J-P, Wen CKC (2019) Citizen science yields first records of Hippocampus japapigu and Hippocampus denise (Syngnathidae) from Taiwan: A hotspot for pygmy seahorse diversity. ZooKeys 883: 83-90. https://doi.org/10.3897/zookeys.883.39662

Short G, Claassens L, Smith R, De Brauwer M, Hamilton H, Stat M, Harasti D (2020) Hippocampus nalu, a new species of pygmy seahorse from South Africa, and the first record of a pygmy seahorse from the Indian Ocean (Teleostei, Syngnathidae). ZooKeys 934: 141-156. https://doi.org/10.3897/zookeys.934.50924

Tiralongo F, Baldacconi R (2014) A conspicuous population of the long-snouted seahorse, Hippocampus guttulatus (Actinopterygii: Syngnathiformes: Syngnathidae), in a highly polluted Mediterranean coastal lagoon. Acta Ichthyologica et Piscatoria 44(2): 99-104. https://doi.org/10.3750/AIP2014.44.2.02

Otters as ocean doctors: how a 40-year watch on Brazil’s coasts reveals hidden threats to estuaries

Neotropical otters are key for estuarine health, providing insights into ecosystem integrity and pollution impacts.

Guest blog post by Dr. Oldemar de Oliveira Carvalho Junior

For four decades, we’ve been quietly watching otters along the southern coast of Brazil. Not just because they’re charismatic and playful, but because they are among nature’s most honest diagnosticians. Just like a doctor checks your pulse, blood, and behavior to assess your health, scientists can use otters to monitor the condition of estuaries, those vital transition zones where rivers meet the sea.

Published in Estuarine Management and Technologies, our new study, ‘Otters as Bioindicators of Estuarine Health,’ synthesizes 40 years of field data from from Projeto Lontra in Brazil’s Peri Lagoon, along with global ecological research. The findings reinforce the role of semi-aquatic mammals as “living sensors” of ecosystem integrity.

This study is part of the topical collection: Otters as Bioindicators of Estuarine Health: Innovations in Monitoring and Management from Tropical Coastal Brazil

Why otters and not another animal?

Neotropical otter (Lontra longicaudis). Photo credit to: Projeto Lontra / Instituto Ekko Brasil

Otters sit at the top of the food chain in estuaries. They need clean water, healthy fish populations, connected habitats, and safe denning sites. If any of these elements falter, otters are among the first to respond, with fewer sightings, changes in their diet, or markers of disease.

While a water sample offers only a fleeting snapshot, otters aggregate environmental signals across time and space.

Neotropical otter with a cub. Photo credit to Projeto Lontra / Instituto Ekko Brasil

In fact, their very presence, or absence, tells a story. In regions where Atlantic Forest fragmentation has severed the connection between land and water, otter sightings have plummeted by 30% in just a decade.

This isn’t just a loss of biodiversity; it’s a warning for everyone downstream. Fewer otters mean degraded waterways, disrupted food webs, and weakened natural buffers against floods and erosion.

A “living record” of pollution

Neotropical otter (Lontra longicaudis) feeding on fish. Video credit to: Projeto Lontra / Instituto Ekko Brasil

The diet of otters consists of 70-80% fish, as well as crabs and other aquatic animals. As they consume prey, they also accumulate pollutants, like heavy metals, microplastics, and industrial chemicals, that have built up in those animals. Their bodies effectively become archives of contamination.

Think of an otter as a biological hard drive: by analyzing its scat (feces), we can reconstruct what pollutants are moving through the estuary, even if they’re invisible to the naked eye.

For instance, in Brazil, we’ve found microplastic fibers in otter droppings from protected lagoons, proof that no coastal system is truly isolated from human impact.

The tropical knowledge gap

Neotropical otter. Photo credit to: Projeto Lontra / Instituto Ekko Brasil

Globally, over 70% of otter research focuses on temperate species like the Eurasian or sea otter. Meanwhile, the Neotropical otter (Lontra longicaudis) receives less than 4% of scientific attention, despite inhabiting the world’s most biodiverse and threatened estuaries.

This imbalance in the research poses a great conservation risk. Tropical estuaries face unique pressures: rapid urbanization, mangrove deforestation, and climate-driven sea-level rise. Without focused research, we risk managing these ecosystems with tools designed for entirely different environments.

Our work aims to close this divide, establishing the Neotropical otter as a key indicator to drive evidence-based conservation across the Global South.

Land-based diseases in aquatic sentinels

Video from trap camera of two Neotropical otters in a shelter. Video credit to: Projeto Lontra / Instituto Ekko Brasil

One of our most striking findings showed that 66% of otters tested positive for Toxoplasma gondii – a parasite shed only by domestic cats. How does a land-based pathogen end up in an aquatic mammal? The answer is through runoff.

The rain washes cat feces from the streets, gardens, and informal settlements into rivers and lagoons. This reveals a sobering truth: even within protected areas, otters are exposed to threats originating far inland. To protect these sentinels of ecosystem health, we must implement integrated management strategies that address sewage overflow, urban runoff, and domestic animal impact.

What comes next?

Neotropical otter inside a shelter. Video credit to: Projeto Lontra / Instituto Ekko Brasil

We’re finalizing the Otter Health Index (OHI), a low-cost toolkit for municipalities, NGOs, and community groups to monitor estuaries using simple metrics: spraint frequency, habitat connectivity, contaminant screening, and local knowledge. It’s designed for places with limited labs but rich ecological insight.

After 40 years of observing otters, we’ve learned this: protecting them isn’t just about saving a species. It’s about safeguarding the intricate web of processes that sustain clean water, fisheries, flood resilience, and human well-being.

Otters aren’t just inhabitants of our estuaries; they are their guardians. If we listen to what they’re telling us, we’ll know exactly what these ecosystems need to survive and thrive.

Original sources:

Carvalho Junior, O., Bez Birolo, A., Tosatti, M., Haddout, S., Ljubenkov, I. and Jayachandran, P.R. eds., (n.d.). Otters as Bioindicators of Estuarine Health: Innovations in Monitoring and Management from Tropical Coastal Brazil. PEstuarine Management and Technologies. doi:https://doi.org/10.3897/emt.coll.317


Birolo, A.B., Tosatti, M., Junior and Assiya Haddout (2026). Otters as bioindicators of estuarine health: Scientific gaps, field-based insights, and a framework for future research. Estuarine Management and Technologies., 3, pp.65–78. doi:https://doi.org/10.3897/emt.3.185117.

Great white sharks in Spain: new record sparks a 160-year review

A juvenile great white shark was caught off Spain, prompting further research confirming its elusive presence in the Spanish Mediterranean.

On April 20, 2023, a juvenile great white shark (Carcharodon carcharias) measuring approximately 210 cm and weighing between 80-90 kg was incidentally caught by local fishermen off the coast of eastern peninsula. This rare encounter, prompted the researchers to dive deep into past records spanning from 1862 to 2023 compiling an extensive review that is now published in the open-access journal Acta Ichthyologica et Piscatoria.

The accidentally caught juvenile great white shark. Photo credit to Báez et al., 2026

The accidental capture – contextualized within a review of records spanning 160 years – revealed that while the Mediterranean great white shark remains as an elusive “ghost” population, it maintains a continued presence in these waters. Currently, the species is listed as Vulnerable on the IUCN Red List, with a declining population trend.

“Determining the presence of juvenile individuals is of particular importance,” says Dr. José Carlos Báez, the study’s lead researcher. “The occurrence of juvenile specimens raises the question whether active reproduction may be occurring in the region.” He further hypothesized. 

The fear of Great White Sharks

Through the examination of records, this study confirms the continued, though sporadic, presence of white sharks in Spanish Mediterranean waters. This research highlights a persistent but infrequent occurrence, with sightings remaining an exceptional event.

Citing H.P. Lovecraft’s famous observation that “the oldest and strongest emotion of mankind is fear, and the oldest and strongest kind of fear is fear of the unknown.” He emphasizes that scientific clarity is the best remedy. “By shedding light on the biology and ecology of the great white shark, research can help replace unfounded myths with genuine understanding.”

Dismantling the Stigma, One Myth at a Time

Video of the accidentally caught great white shark. Credit to Báez et al., 2026

With Great White Shark populations in decline, researchers emphasize that long-term observation programs are vital to understanding the species’ biology in the Mediterranean. By pairing direct sightings with advanced tracking methods, evidence-based strategies can be developed for the conservation of this iconic apex predator.

“The main idea I want to convey to the public is that these large marine animals have a fundamental role in marine ecosystems. As highly migratory pelagic species, they redistribute energy and nutrients across vast distances. They serve as nature’s scavengers – by consuming carrion, they keep ecosystems clean. Even in death, their descent to the seafloor provides a critical pulse of nourishment for deep-sea communities.

concludes Báez.

Research article:

Báez, J.C., Puerto, M.A., Torreblanca, D., Varela, J.L., Carmona, L. and Macías, D. (2026). New record of white shark, Carcharodon carcharias (Elasmobranchii, Lamniformes, Lamnidae), from the Mediterranean Spanish coast. Acta Ichthyologica et Piscatoria, 56, pp.27–31. doi:https://doi.org/10.3897/aiep.56.173786.

Using AI to Uncover the Secret Lives of Fungi

AI holds the potential to automatically identify fungal versatility from the available scientific literature.

Fungi are the hidden architects of our ecosystems, acting as everything from helpful partners for plants to aggressive decomposers that recycle dead wood. However, many fungi don’t stick to just one job; they can switch lifestyles depending on their environment.  

Understanding this flexibility is vital for predicting how forests and farms will react to climate change. Unfortunately, the information researchers need is buried in decades of scientific papers that would take too long to comb through manually. 

A new study led by Northern Arizona University doctoral student Beatrice M. Bock and published in the open-access journal Research Ideas and Outcomes demonstrates how AI can solve this problem. By using a specialized language model called BioBERT, Bock developed an automated workflow that assesses scientific abstracts and accurately identifies whether a fungus has a single lifestyle or a dual, flexible one. 

A high-accuracy hack 

Bock said that for years, mycologists have relied on manual databases to track what different fungi do in the environment. While these tools are essential, they are difficult to keep updated as new research is published every day. 

“Manually identifying fungal versatility from the literature is time-consuming and difficult to scale. By using machine learning, we can now scan thousands of papers in just a few minutes to flag species that might be switching roles—such as a fungus that normally helps a plant grow but also turns into a decomposer when the plant dies.” 

Beatrice M. Bock

The pilot study tested four different AI models to see which was best at understanding the nuances of biological language. The top-performing model, BioBERT, achieved nearly 90% accuracy in identifying fungal lifestyles. 

What did BioBERT have that the other models didn’t? For one, it had the power of capitalization. Bock found that “cased” models—those that recognize capital letters—performed significantly better than those that did not. That’s likely because capital letters often signal species’ scientific names, like Fusarium, which are crucial for AI to understand the context of the research. 

The path ahead 

Bock said that in a commitment to transparency, she has made all the code and data available for free online, allowing other scientists to build upon her work and track traits in other organisms, like insects or plants. 

While Bock’s study focused on a small group of papers as a proof-of-concept, it opens the door for much larger projects. Future versions of the tool could predict how a fungus’s behavior might change under specific environmental conditions, such as drought or extreme heat. 

“As fungal trait databases continue to grow in importance for biodiversity assessments, automated text mining offers a path toward more efficient, consistent and comprehensive trait annotation.”

Beatrice M. Bock

Original sources:

Bock B (2026) Automated extraction of fungal trophic modes from literature using BioBERT: an open pilot workflow. Research Ideas and Outcomes 12: e176590. https://doi.org/10.3897/rio.12.e176590

Story originally published by: EurekAlert! (2026). Using AI to uncover the secret lives of fungi. [online] Available at: https://www.eurekalert.org/news-releases/1114462 [Accessed 2 Feb. 2026]. Republished with permission.

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Corals’ Boldest Cousins: UH Scientists Discover Marine Creatures Bending the Laws of Evolution

A new Frontiers of Biogeography study shows zoantharian hexacorals defy biogeographic norms with narrow genetic differences across the Atlantic and Indo-Pacific.

Guest blog post by Dr. Maria “Duda” Santos and Maria Frostic

In the realm of marine biogeography, there is a widely held scientific principle: the Atlantic and Indo-Pacific oceans are worlds apart. If you dive in Brazil and then in Okinawa, you expect to see entirely different groups of fish and coral. But according to a new global study published today in Frontiers of Biogeography, one group of colorful hexacorals, anemone-like creatures—known as zoantharians—is breaking all the rules.

The study, led by Dr. Maria “Duda” Santos of the UH Mānoa Hawaiʻi Institute of Marine Biology (HIMB) ToBo Lab and the University of the Ryukyus, began with a moment of “déjà vu” underwater. 

Diver in Malaysia looking at a coral reef
Underwater view in a Malaysian coral reef with Duda searching for zoantharian species. Photo by Sam Webster.

“During my first dive in Okinawa, I was surrounded by a multitude of species I had never seen in my homeland of Brazil. But then I saw the zoantharians. They looked exactly like the ones back home—the same colors, shapes, and sizes. It was striking.”

shares Dr. Santos

While the Indo-Pacific typically hosts ten times the species diversity of the Atlantic for most reef animals, this research found that the genetic and morphological divergence between oceans for these creatures is surprisingly narrow.

The Secrets of the Ultimate Travelers

Zoantharians from different parts of the ocean that surprisingly show narrow evolution despite the distance
Sibling zoantharians from the Indo-Pacific (A) and the Atlantic (B) oceans. Images by Dr. Maria “Duda” Santos.

The researchers suggest that zoantharians may be the ultimate oceanic travelers. Their secret likely lies in high dispersal via an “epic” larval phase, where young zoantharians can survive in open water for over 100 days, paired with an ability to “raft” across ocean basins by hitchhiking on floating objects.

Furthermore, an unusually slow evolutionary rate appears to keep distant populations looking and acting like siblings, even after millions of years of separation by continental barriers.

This discovery has major implications for the future of our oceans. As climate change stresses traditional stony corals, zoantharians are increasingly moving in to fill the void. 

“In habitats impacted by stress, some zoantharian species can outcompete stony corals. We are seeing ‘phase shifts‘ where reefs once dominated by corals are being taken over by zoantharians. Understanding how they spread helps us forecast what the reefs of the future will look like.”

explains Dr. Santos

A Global Atlas for a Changing Ocean

This landmark study represents a massive international effort, uniting a team from Hawai’i, Okinawa, Russia, Brazil, Hong Kong, Taiwan, and Indonesia. By combining DNA data and records from Mexico to the Philippines, the team has provided the first-ever global “atlas” for a group of animals that has remained in the shadows of their more famous coral cousins for decades. This map of the past and present provides a vital baseline for monitoring how marine life will navigate a warming world.

Original source

Santos, M.E.A., Kise, H., Fourreau, C.J.L., Kiriukhin, B., Kitahara, M.V., Baker, D.M., Toonen, R.J., Liu, P.J., Chang, A., Tu, T.-H., Widiastuti, Agustini, K.M.P., Bowen, B.W. and Reimer, J.D. (2026). Global biogeography of zoantharians indicates a weak genetic differentiation between the Atlantic and Indo-Pacific oceans, and distinct communities in tropical and temperate provinces. Frontiers of Biogeography, 19. doi: https://doi.org/10.21425/fob.19.174247

Biodiversity loss hidden in global staple food trade shows data spanning 27 years

By translating global food trade flows into biodiversity loss transfers, the dataset maps how, and through which trade links, ecological impacts shift across borders.

Global food trade is essential for food security but its ecological consequences often remain unseen. A new data paper published in One Ecosystem introduces a global long-term dataset, quantifying biodiversity loss embodied in the international trade of staple food crops. As such, this dataset offers a novel perspective on how food trade redistributes environmental pressures worldwide.

Developed by Dr Zhuofan Huang, Dr Zhenglei He and Zelin Xing of the Guangdong University of Technology in Guangzhou, China, the dataset spans 1995–2022 and focuses on four major staple crops: wheat, soybean, rice and maize. By integrating bilateral trade data from UN Comtrade with agricultural production statistics from FAOSTAT and biodiversity loss intensity factors expressed as the Potential Disappeared Fraction (PDF), the dataset translates food trade flows into quantifiable biodiversity loss transfers between countries.

The resulting global network includes 157 countries and up to 91,414 trade relationships, capturing the dynamic evolution of biodiversity loss embedded in staple food trade over nearly three decades. Unlike previous studies that examine agricultural biodiversity impacts at national or sectoral levels, this dataset explicitly maps how biodiversity loss is transferred across borders through international trade.

Global biodiversity loss embodied in staple food trade (1995–2022)

Initial analyses reveal a strong upward trend in biodiversity loss embodied in global staple food trade. Among the four crops, soybean trade shows the most rapid increase, with biodiversity loss rising more than sixfold from 1995 to 2022, and surpassing wheat as the dominant contributor in recent years. The findings also highlight the central role of major agricultural producers and traders (including the United States, Brazil, China, Australia and Argentina) in shaping global biodiversity loss patterns.

Major trade pathways transferring biodiversity loss in global staple food trade between 1995-2022 (Huang et al., 2026)

The authors have openly released this dataset, therefore providing a valuable resource for interdisciplinary research and policy analysis. The data can support assessments of environmental responsibility in food supply chains, help identify high-risk trade pathways, and inform the development of more sustainable and equitable global food trade policies – these factors will in turn contribute to biodiversity conservation and the achievement of the UN Sustainable Development Goals 15 (Life on Land).

Original source:

Huang Z, He Z, Xing Z (2026) Dataset of Biodiversity Loss in Global Staple Food Trade, 1995-2022. One Ecosystem 11: e159884. https://doi.org/10.3897/oneeco.11.e159884

More Than 55% of Cerrado Native Vegetation Already Lost, New Review Reveals

With 55% of its native habitat gone, the Cerrado is in crisis. Preserving this biodiversity hotspot demands immediate reform and the protection of Indigenous rights.

Guest blog post by Cássio Cardoso Pereira

“In addition to surviving some of the poorest soils in intertropical Brazil, the vegetation of the Cerrado has achieved the ecological feat of withstanding wildfires, rising from its own ashes like a kind of phoenix among Brazil’s ecosystems. It cannot, however, withstand the violent technological artifices invented by so-called civilized men.”

Aziz Ab’Saber, 2003 (translated)

Often overshadowed by the Amazon, the Cerrado is the second-largest Ecodomain in South America. Despite covering 24% of the territory and sustaining major watersheds, it has historically been sidelined in global conservation dialogues.

Our detailed review recently published in Nature Conservation warns that this biodiversity hotspot is currently facing a massive, multi-faceted ecological crisis. Despite its significance, the region has seen more than 55% of its native vegetation converted, an area exceeding 1 million km², with the vast majority of this destruction occurring within the last five decades.

Detailed maps of the Cerrado Ecodomain in Brazil.
Land use and land cover (LULC) in the Cerrado Ecodomain in 1985 and 2023, revealing significant changes in the spatial structure of the territory. An intensification of human activities can be observed, with emphasis on agricultural expansion,
which resulted in the significant replacement of native vegetation by alternative uses. This process represents an accelerated landscape transformation over the last four decades. These maps were made using the Cerrado shapefile developed by Cássio Cardoso Pereira, with LULC data available from MapBiomas (2024).

While recent data suggests a slight reduction in annual deforestation rates, the accumulated loss continues to climb, making the Cerrado the Ecodomain in Brazil with the greatest loss of native vegetation.

Graph presenting the annual clearing in Cerrado Ecodomain.
Annual clearing in the Cerrado (2001–2025) according to PRODES (INPE 2025). Bars represent the total area cleared each year (km²), with colors ranging from dark orange (highest values) to light orange (lowest values), indicating relative variation in intensity. Arrows indicate the percentage change compared to the previous year: increases (↑, red), decreases (↓, green), and stability (→, black, 0.0%). These data do not detect degradation, only complete removal of natural vegetation. Annual data refer to the so-called “reference year”, which runs from August of one year to July of the following year, based on satellite images with a resolution of 10 to 30 meters. The icons used in this figure are from Wikimedia licensed under CC BY-SA 4.0. Figure design: Cássio Cardoso Pereira.

This expansion is driven by a combination of agricultural and urban growth, mining, and land speculation, creating a landscape that is increasingly fragmented and ecologically compromised.

Inverted forest and hidden carbon

One of the things that make Cerrado truly unique is its “inverted forest“. Unlike tropical rainforests that store their biomass in high canopies, the Cerrado has achieved an ecological feat of survival by storing approximately 90% of its carbon belowground through massive, deep root systems. This underground network makes the Ecodomain a critical carbon sink and a primary regulator of water.

Schematic of the inverted forest carbon sink capacities in the Cerrado Ecodomain.
Schematic representation of the distribution of carbon stocks in the Cerrado, characterized as an “inverted forest” due to the predominance of biomass and carbon belowground. Estimates were obtained from Terra et al. (2023). Figure design: Walisson Kenedy-Siqueira.

However, misguided restoration efforts that focus solely on planting exotic trees in naturally open areas can further exacerbate this issue, highlighting the need for restoration strategies that prioritize ecological functionality and native seed banks over simple afforestation.

Ecosystem diversity and conservation challenges

However, it is not just the vast tropical savanna in Cerrado that makes up this inverted forest, but the complex and interdependent mosaic of grasslands, savannas, and forests, each with distinct structures, ecological processes, and vulnerabilities. Treating it as homogeneous invisibilizes both grassland and forest formations, complicating effective conservation policies.

For example, natural grasslands, especially in the montane Campos Rupestres, occupy limited areas, harbor high endemism, and face strong pressures from mining, biological invasions, and increased fire. Whilst savannas, although dominant in the area, have been widely converted into monocultures, exotic pastures, and forestry, compromising ecological integrity.  

The major anthropogenic threats to the ecosystems of Cerrado Ecodomain
Main anthropogenic threats to the Cerrado resulting from land-use changes, ranked by impact on each ecosystem type (I–III: grassland, savanna, and forest). The ecosystems illustrated are according to Ribeiro and Walter (2008). For more details on each ecosystem. Figure design: Walisson Kenedy-Siqueira.

Even though some species are adapted to natural fire, many ecosystems, such as forests, the marshland formations Veredas, and the montane Campos Rupestres, are highly vulnerable. Exotic species invasions and increased frequency and intensity of fires exacerbate ecological losses even without direct deforestation. We’ve found out that nearly all fires in the Cerrado are human-induced and occur outside natural regimes, causing cumulative degradation.

Threatened biodiversity and conservation gaps

Our research highlights a troubling pattern of ‘silent extinctions’ across the Cerrado. While this Ecodomain is home to thousands of unique plants and animals, we have identified a massive gap in how these species are monitored. Plants and invertebrates are the most threatened yet the least studied. This means species are vanishing before they can even be scientifically documented. Current policies are failing because they rely on incomplete data; we cannot protect what we have not yet cataloged. To prevent total collapse, we must expand our conservation criteria to protect not just individual species, but the complex ecological interactions that sustain the region’s water and soil.

The threatened species in Cerrado Ecodomain
Percentage distribution of threatened species among different biological groups in the Cerrado. The information was adapted from the IUCN Red List (2024), the Flora and Funga of Brazil portal (2024), the official national list of threatened species by MMA (2022), terrestrial vertebrate data from Vieira-Alencar et al. (2025), freshwater fish data from Lima and Ribeiro (2011), and invertebrate data from Embrapa (2023). Figure design: Walisson Kenedy-Siqueira.

Cerrado’s water crisis

The environmental crisis in the Cerrado is also a “silent water crisis” that threatens Brazil’s national security. The Ecodomain sustains the country’s main watersheds and major aquifers, yet this balance is being disrupted by irrigated agriculture, agrochemical contamination, and dam construction. Excessive surface and groundwater withdrawal is already leading to reduced river flows and the degradation of Veredas, which are essential for water regulation.

Paradoxically, the very sectors that drive this degradation, such as agribusiness and energy production, are the most dependent on these water resources, creating a cycle of increasing water insecurity. Protecting the Cerrado’s riparian zones and aquifers is no longer just an environmental concern but a prerequisite for the survival of the regional economy and climate resilience.

Disconnect between law and reality

The Cerrado is facing a dangerous disconnect between environmental law and ecological reality. Our research reveals that current protection is startlingly thin: while we cataloged 706 Conservation Units, they cover only 8% of the Ecodomain, with less than 3% under strict protection.

To assist researchers and policymakers, we have compiled an unprecedented dataset of these units, including the often overlooked Private Natural Heritage Reserves (RPPNs)  and crucial ecotones, available at: https://doi.org/10.3897/natureconservation.61.168273.suppl1.

However, data alone isn’t enough. The Brazilian Forest Code, specifically the 20% Reserva Legal (RL) and the narrow 30-meter Áreas de Preservação Permanent (APPs) are ecologically insufficient. These leave vital formations like Veredas and Campos Rupestres as isolated, vulnerable fragments.

To prevent ecosystem collapse and secure Brazil’s water supply, we advocate for urgent reforms: increasing RL requirements to at least 35%, expanding protection zones to reflect biological reality, and enforcing strict traceability to decouple agricultural production from habitat loss.

Recognition and protection of Indigenous lands

Two Kayapó indigenous people
Kayapó people from the state of Pará. Their lands are located in the Amazon, but include a Cerrado enclave, which is shown in the review. Photo credit to: Adriano Adriano Jerozolimski

Beyond legal designations, we emphasize that the future of the Cerrado depends on recognizing the rights of Indigenous peoples, whose traditional knowledge and sustainable land management have maintained the ecosystem’s balance for millennia.

For instance, recent laws such as the Marco Temporal and agribusiness proposals threaten to reduce their territories and accelerate biodiversity loss, making it urgent to protect and fully recognize these lands to conserve the Cerrado and its ecological resilience.

Mobilizing knowledge and adding value

Effective conservation requires recognizing the Cerrado as a biodiversity hotspot with dedicated legal instruments capable of protecting its full ecological heterogeneity.

Moving forward, the extractive logic of the past must be replaced with with regenerative systems, prioritizing conservation, restoration, and biodiversity-based economic alternatives, including agroforestry, payments for ecosystem services, fiscal incentives such as ICMS Ecológico. Ultimately, these measures will help promote conservation, social justice and sustainable certifications that recognize the Cerrado’s biodiversity as a core economic asset

Original publicaiton:

Pereira, C.C., Walisson Kenedy-Siqueira, Maia, L.R., da, V., Arantes-Garcia, L., Fernandes, S., França, G., Carvalho, G., Rodrigues, J., Salm, R. and Fearnside, P.M. (2026). The Cerrado crisis review: highlighting threats and providing future pathways to save Brazil’s biodiversity hotspot. Nature Conservation, 61, pp.29–70. doi: https://doi.org/10.3897/natureconservation.61.168273

School student discovered a new dung beetle in Xinjiang, China

New dung beetle, Cheiroplatys aiweiae, discovered by a middle school student from China.

In the rugged hills of Shiren Gou, Urumqi, in China, a field research trip turned into a scientific discovery for middle school student Wang Yuheng. In June, 2022, while exploring, the student spotted an insect with an unusual metallic luster on its body.

After several days of comparisons, he made a bold claim: this was a new species that he had never seen before!

Close up photos of the newly discovered dung beetle Cheironitis aiweiae from China.
Photos of Cheironitis aiweiae (Wang et al., 2025)

To test Wang’s statement, his school’s science teacher teamed up with Zhang Xin, a PhD biologist from the Xinjiang Institute of Ecology and Geography at the Chinese Academy of Sciences. Their detailed analysis confirmed it – this was a new species of dung beetle from the genus Cheironitis.

The discovery was published in the open-access journal ZooKeys, marking the first record of Cheiroplatys aiweiae in China, as well as the first documented distribution of Cheironitis moeris in the country.

The young discoverer Wang Yuheng.
Photo of Wang Yuheng. Credit to the Xinjiang Production and Construction Corps No. 2 Middle School WeChat Official Account

However, turning the discovery of the new species into a published paper wasn’t easy for Wang. He was faced with language barriers, struggled with report structure, and grappled with complex scientific terms. Undeterred, he consulted existing literature, double-checked data, and worked through multiple revisions until the manuscript was finally ready for publication.

By tradition, the discoverer of a new species has the right to name it. Endearingly, Wang chose the name Cheiroplatys aiweiae after his mother’s name, honoring her unwavering support throughout the research and publication process.

Original source:

Wang, Y., Montreuil, O. and Coppo, P. (2025). A new species of Cheironitis van Lansberge, 1875 (Coleoptera, Scarabaeidae, Onitini) and the first record of Cheironitis moeris (Pallas, 1787) from China. ZooKeys, 1265, pp.151–158. doi: https://doi.org/10.3897/zookeys.1265.174240

Herbarium Records Lead Bucknell Researcher to a New Plant Species in the Australian Outback

Australian botanists have newly identified Solanum nectarifolium, or the Tanami Bush Tomato, from historical specimens collected near the northern edge of the Tanami Desert.

Specialized Organs for Feeding Ants are First of Their Kind.

LEWISBURG, Pa. — A recent study led by Bucknell University Professor Chris Martine, biology, the David Burpee Professor in Plant Genetics & Research, has identified and described a new species of bush tomato with a special connection to ants — a taxonomic journey sparked by unusual specimens held in Australian herbarium collections.

The study, co-authored by a set of Australian botanists and Jason Cantley — the former Burpee Postdoctoral Fellow in Botany at Bucknell who is now Associate Professor of Biology at San Francisco State University — was published in the open-access journal PhytoKeys and underscores the critical role that natural history collections play in biodiversity science. The new species, Solanum nectarifolium, or the Tanami Bush Tomato, was named for the location of its original collection area — the northern edge of the Tanami Desert — and for the uniquely conspicuous nectar-producing organs on the undersides of its leaves.

The newly found Tanami Bush tomato from the Tanami Desert in Australia.
Solanum nectarifolium, a newly-described species of Australian bush tomato. Photo credit: Kym Brennan. 

Martine first had an inkling that something was unusual about the plants from that region of the Northern Territory while working on a project with another former Burpee Postdoc, Angela McDonnell, now an Assistant Professor at St. Cloud State University. The pair included DNA extracted from two herbarium specimens representing Solanum ossicruentum, a species known as the Blood Bone Tomato that the Martine Lab described in the same journal in 2016, in an ongoing analysis meant to build a new bush tomato evolutionary tree.

“We couldn’t understand why the two collections of the same species kept showing up in different parts of the tree,” says Martine. “I had collected one of them and was certain that it represented Solanum ossicruentum, so I reached out to the person who collected the other one, David Albrecht, and asked whether he thought the plants he saw in 1996 at a place called Jellabra Rockhole could be something else.”

Albrecht, Senior Botanist at the Northern Territory Herbarium at Alice Springs, suggested that the best way to know would be for botanists to revisit that remote region of the northwestern Tanami Desert and see for themselves. Martine, who had participated in seven collecting expeditions to northern Australia since 2004, wasn’t disappointed.

“I was kind of hoping he’d tell me that,” Martine says. “Because I was already planning some new fieldwork in the Northern Territory and this would give me a great season to visit an area I had never been to before. But to really be prepared for a trip like that, I first needed to understand what other botanists had recorded and collected there in the past – and there is only one surefire way to do that: check what is in the herbarium collections.”

So Martine started by using the Australasian Virtual Herbarium (AVH), a database of every plant specimen held in every herbarium in Australia. He searched for collections made of Solanum ossicruentum and a similar species called Solanum dioicum in the northern Tanami, finding 15 records for specimens gathered as far back as 1971.

Map showing distribution of Solanum nectarifolium sp. nov. and S. ossicruentum based on accessions held at the Northern Territory Herbarium, Palmerston (DNA), the Western Australian Herbarium (PERTH), and the National Herbarium of New South Wales (NSW). Credit: Martine et al., 2025

“It was a really interesting distribution of points on the map, too,” Martine says. “These were far south of the other records for Solanum ossicruentum, with hundreds of miles of ‘empty’ country between the two clusters. I couldn’t wait to get to Australia to see what those Tanami plants looked like.”

In May 2025 Martine headed to Australia to meet his team for the trip: Cantley and paper coauthors Kym Brennan, Aiden Webb, and Geoff Newton, all associated with the Northern Territory Herbarium at Palmerston. But, first, Martine made a stop in another plant collection in the southwestern city of Perth.

“The visit to the Western Australian Herbarium was my first chance to spend a bunch of time with some of the actual specimens that I had earmarked based on the data in AVH,” Martine explains. “And what I saw there legit blew my mind.”

Every specimen looked similar to Solanum ossicruentum, except for a few subtle characteristics – and one thing that Martine had never seen in more than two decades of Outback botanizing.

Leaf of Solanum nectraifolium.
The veins on the leaf of Solanum nectarifolium, showing the extrafloral nectaries (EFNs). Phtoo credit: Kym Brennan.

“On the backs of the leaves, along the veins, were these visible round disks,” Martine notes. “They were each around a half-millimeter wide, really obvious, and the only bush tomato specimens that had them – we’re talking hundreds and hundreds of collections – were the ones from the northern Tanami.”

Martine thought they could be extrafloral nectaries (EFNs), non-flower organs on a plant that exude sweet liquid, typically as a means to attract ants that might protect the plants from herbivores. These were known to exist in a few Australian bush tomatoes, but those are tiny and have only been confirmed with microscopes. EFNs that could be seen without magnification would be something truly novel.

A few days later, Martine was in the herbarium at Palmerston and found the same pattern: more visible disks and only on plants from that same geographic area. Then he noticed that the most recent collection, from 2021, had been made by Kym Brennan – a renowned field biologist with an expertise in photography who was preparing for their trip in the next room.

“I ran in there and asked whether he remembered anything unusual about that collection – and before I could finish my explanation for why, he was already showing me an incredible photo of the leaves of that same plant. They were positively oozing with shiny, round droplets of nectar. And all from those disks on the veins.” 

Oozing nectar from underneath the leaf of the newly found Tanami Bush Tomato.
The oozing extrafloral nectaries (EFNs) on the underside of the Solanum nectarifolium leaf. Photo credit: Kym Brennan

Eight days and more than 1000 kilometers of driving later the team arrived near Brennan’s collection site 50 kilometers southwest of the community of Lajamanu, right along the edge of the unpaved Lajamanu Road.

“This was more-or-less the same place where others had collected it in the early 1970s, so we were cautiously optimistic that we’d not only find it there again, but that the plants would have the flowers and fruits on them that we needed to describe this as a new species,” explains Martine. “But it’s a harsh environment and the abundance of bush tomatoes is often dependent on fire occurrence. Sometimes you get to a place and there is nothing but old gray stems. Other times there are more happy plants than you can count. In this case, it was the latter situation!”

Habitat of the Australian Tanami Bush Tomato.
Habitat of Solanum nectarifolium at the type locality. Photo credit: Aiden Webb.

The team got to work taking notes, making measurements, and shooting photographs. And then Cantley called for Martine to come over to the plant he was examining. There were ants all over the leaf undersides, avidly moving from disk to disk and probing them for nectar. Hypothesis confirmed.

The collaborators decided on the scientific name “nectarifolium” – which translates to “nectar leaf,” for obvious reasons – and the English-language name Tanami Bush Tomato. Martine then contacted a few experts about the conspicuous nature of the EFNs and whether that has been seen anywhere else in the genus Solanum, a group of around 1200 species that includes the tomato, potato, and eggplant.

“As far as we know, this is the first Solanum species to be described as having extrafloral nectaries that you can see with your naked eye. That’s a pretty cool finding – and it all started with the examination of specimens that have been waiting in herbaria for as long as a half-century for someone to come along and take a closer look.”

Bucknell’s own Wayne E. Manning Herbarium, which holds approximately 25,000 plant specimens, now includes new samples of the Tanami Bush Tomato. But the official holotype remains at the Northern Territory Herbarium in Palmerston — almost 10,000 miles away from Bucknell’s campus.

Five different pictures of the newly discovered plant Solanum nectarifolium.
Habit and morphology of Solanum nectarifolium. Photo credit: Kym Brennan and Chris Martine.

“The Manning Herbarium may be small, but every specimen is a snapshot of biodiversity,” Martine says. “These collections allow us to study where species occur, how they’ve changed over time, and — in cases like this — even help discover new ones.”

The publication of the new species comes amid broader concern over the fate of natural history collections, such as Duke University’s recently announced closure of its herbarium housing more than 800,000 specimens. Martine and his colleagues agree that such closures could hinder future discoveries and conservation efforts.

Martine, a leading expert on Australian bush tomatoes, was recently elected president-elect of the Botanical Society of America. He will begin his term as president following the organization’s annual meeting in August 2026.

“It still doesn’t feel real and probably won’t until I start my term just after Botany 2026,” Martine says. “But I promise to do my best because plants are awesome and so are botanists.”

Original study:

Martine, C.T., Brennan, K., Cantley, J.T., Webb, A.T. and Newton, G. (2025). A new dioecious bush tomato, Solanum nectarifolium (Solanaceae), from the northern Tanami Desert, Northern Territory, Australia, with reassessment of S. ossicruentum and a change in the circumscription of S. dioicum. PhytoKeys, 268, pp.183–199. doi: https://doi.org/10.3897/phytokeys.268.169893