Author: Pensoft Editorial Team

An invasive plant may cost a Caribbean island 576,704 dollars per year

Guest blog post by Wendy Jesse

Coralita overgrowing vegetation. Photo from https://www.wur.nl/en/show/invasive-plants-in-caribbean-netherlands.htm

A recent study in One Ecosystem has estimated the severe loss of ecosystem service value as a result of the widespread invasion by the plant species Coralita (Antigonon leptopus) on the Caribbean island of St. Eustatius. The results illustrate the drastic impact that a single invader can have on the economy of a small island and inform policy makers about priority areas for invasive species management.

See for full article: Huisman, S., Jesse, W., Ellers, J., & van Beukering, P. (2021). Mapping the economic loss of ecosystem services caused by the invasive plant species Antigonon leptopus on the Dutch Caribbean Island of St. Eustatius. One Ecosystem, 6, e72881. https://doi.org/10.3897/oneeco.6.e72881

The invader: Coralita

  • Flowering coralita, creeping vertically over fences and horizontally across the ground.
  • Coralita intertwined with electricity box and cables. Photo by Adam Mitchell

Coralita is a fast-growing, climbing vine with beautiful pink or white flowers. Originally from Mexico, it was introduced as a popular garden plant to many Caribbean islands and around the world. Its fast-growing nature means that it can outcompete most native species for terrain, quickly becoming the dominant species and reducing overall diversity (Jesse et al. 2020, Nature Today 2020, Eppinga et al. 2021a). This is especially the case on St. Eustatius, where published ground surveys indicate that the plant already appears on 33 percent of the island.

Losses of ecosystem services

Coralita overgrowing cars. Photo by Rotem Zilber

We estimated the total terrestrial ecosystem service (ES) value on St. Eustatius to be $2.7 million per year by mapping five important terrestrial ecosystem services: Tourism, Carbon sequestration, Non-use (i.e., intrinsic biodiversity) value, Local recreational value, and Archeological value. Subsequently, we calculated Coralita-induced loss of ecosystem services under two realistic distributional scenarios of Coralita cover on the island: 3% of island dominantly covered (based on Haber et al. 2021, Nature Today 2021) and 36% dominant cover (if entire range would reach dominant coverage), causing an annual ES value loss of $39,804 and $576,704 respectively. The highest ES value (17,584 $/ha/year) as well as the most severe losses (3% scenario: 184 $/ha/year; 36% scenario: 1,257 $/ha/year) were located on the dormant Quill volcano; a highly biodiverse location with popular hiking trails for locals and tourists alike.

Consequences for policy makers and practitioners

Coralita blocking water a drainage channel. Photo by Wendy Jesse.

There is an urgent need for studies such as this one that help to bridge the gap between academia and policy planning, as these translate abstract numbers into intuitive information. Instead of invasive species being just a biological term, direct impacts on people’s value systems and sources of income immediately strike a chord. I experience this on a daily basis, because in addition to being a coauthor on this paper, I currently work as a policy employee in nature protection and management.

Coralita overgrowing archeological heritage on St. Eustatius. Photo from St. Eustatius Center for Archeological Research (SECAR)

This study helps to prioritize locations for invasive species prevention, management, eradication, and restoration. It is imperative that invasive species do not reach locations of high ecosystem service value. Management of isolated satellite patches of Coralita close to locations of high ES value will likely be most effective in halting the plant’s invasive spread (Eppinga et al. 2021b). Setting up a targeted monitoring and rapid response strategy, as well as legislation for biosecurity measures to prevent other invasive species from entering the island, would likely help to reduce impacts on the important ecosystem services on St. Eustatius.

References

Academic literature:

Eppinga, M. B., Haber, E. A., Sweeney, L., Santos, M. J., Rietkerk, M., & Wassen, M. J. (2021a). Antigonon leptopus invasion is associated with plant community disassembly in a Caribbean island ecosystem. Biological Invasions, 1-19.

Eppinga M, Baudena M, Haber E, Rietkerk M, Wassen M, Santos M (2021b) Spatially explicit removal strategies increase the efficiency of invasive plant species control.

Ecological Applications 31 (3): 1‑13. https://doi.org/10.1002/eap.2257Haber E, Santos M, Leitão P, Schwieder M, Ketner P, Ernst J, Rietkerk M, Wassen M, Eppinga M (2021) High spatial resolution mapping identifies habitat characteristics of the invasive vine Antigonon leptopuson St. Eustatius (Lesser Antilles). Biotropica 53 (3): 941‑953. https://doi.org/10.1111/btp.12939

Jesse, W. A., Molleman, J., Franken, O., Lammers, M., Berg, M. P., Behm, J. E., … & Ellers, J. (2020). Disentangling the effects of plant species invasion and urban development on arthropod community composition. Global change biology, 26(6), 3294-3306.

Blog posts on Nature Today website:

van Maanen, G. Molleman, J., Jesse, W.A.M. (2020) Drastic effects of coralita on the biodiversity of insects and spiders. Nature Today. naturetoday.com/intl/en/nature-reports/message/?msg=26339

Dutch Caribbean Nature Alliance (2021) Using satellite imagery to map St. Eustatius’ coralita invasion. Nature Today. naturetoday.com/intl/en/nature-reports/message/?msg=28317

In the Atlantic Forest, the lowland tapir is at risk of extinction

Lowland tapir populations in the Atlantic Forest in South America are at risk of almost complete disappearance, scientists have estimated. The main long-term threat to their well-being is population isolation, as hunting and highways keep populations away from each other. Urgent measures need to be taken to connect isolated populations and ensure the long-term conservation of tapirs, warn the authors of a new study published in the open-access journal Neotropical Biology and Conservation.

Lowland tapir populations in the Atlantic Forest in South America are at risk of almost complete disappearance, scientists have estimated. Weighing up to 250 kg, the animal can adapt to most habitats in South America—but its populations continue to decline across its range.

Today, its survival is seriously threatened: it can be found in just 1.78% of its original distributional range in the Atlantic Forest biome, which covers parts of Brazil, Argentina and Paraguay. The main long-term threat to its well-being is population isolation, as hunting and highways keep populations away from each other.

Lowland tapir. Photo by Patricia Medici

Urgent measures need to be taken to connect isolated populations and ensure the long-term conservation of tapirs, warn the authors of a new study on the distribution and conservation status of lowland tapirsin the South American Atlantic Forest, published in the open-access journal Neotropical Biology and Conservation. 

The research was done by Kevin Flesher, PhD, researcher at the Biodiversity Study Center, Michelin Ecological Reserve, Bahia, and Patrícia Medici, PhD, coordinator of the Lowland Tapir Conservation Initiative, a project developed by the Institute for Ecological Research in Brazil, and chair of the Tapir Specialist Group at the Species Survival Commission in the International Union for Conservation of Nature.

 “Of the 48 tapir populations identified during the study, between 31.3% and 68.8% are demographically unviable (low number of individuals), and between 70.8% and 93.8% of the populations are genetically unviable (low gene flow). Only 3-14 populations are still viable in the long run when both criteria are considered. The evidence suggests that with the appropriate conservation actions, the lowland tapir could be broadly distributed throughout the Atlantic Forest,” says Kevin Flesher. 

Lowland tapir. Photo by Alexander Blanco

“Tapirs have low reproductive potential, including a long reproductive cycle with the birth of just one young after a gestation period of 13-14 months and intervals of up to three years between births. Our populational simulations clearly show how, in the case of small populations, even the loss of a single individual per year can result in rapid extinction of an entire local population,” adds Medici. 

Lowland tapir. Photo by Bill Konstant

Kevin Flesher dedicated 15 years to visiting 93 reserves in the Atlantic Forest, talking to people and analyzing 217 datasets, before he compiled the necessary data to design conservation actions that can ensure the survival of tapirs in the area. 

The states of São Paulo and Paraná in Brazil have the largest number of remaining populations: 14 and 10, respectively. The two largest populations are in Misiones, Argentina, and in the neighboring Iguaçu and Turvo reserves, in Paraná and Rio Grande do Sul, Brazil.

“As far as our knowledge goes, there is no evidence of movement of tapirs between these populations,” points out Medici.

  • Primary forest
  • Deforestrated agricultural land
  • Reserve edge
  • Reserve edge
  • Agricultural matrix
  • Forested mountain
A glimpse of the tapir’s diverse habitats. Photos by Kevin Flesher

The distance between population fragments, however, is not what is stopping them.

“The central problem is the multiple threats they face while crossing the habitat,” explains Flesher. Highways are one major obstacle that limits the access of tapirs to forests with adequate habitat. “For example, the heavy traffic on highway BR-101 (which cuts the Brazilian Atlantic Forest from North to South) is a death trap to wildlife. Tapirs often die when attempting to cross it,” explains Medici. 

The construction of highways and expansion of traffic in and around natural areas is a serious threat to large tapir populations that might otherwise have the chance to thrive, like those in Misiones, Argentina, and Serra do Mar, Brazil. 

“Roadkill is a significant cause of death in six of the eight reservations in which highways cross tapir populations, and the expansion of the roadway grid in the country threatens to cause population fragmentation in at least four populations,” points out Flesher. This is why finding ways to allow tapirs to cross highways safely is an urgent conservation priority.

Lowland tapir. Photo by Patricia Medici

The results of the study, however, give cause for “cautious optimism” for the future of tapirs in the area: after decades of dedicated conservation efforts, the situation is starting to improve. 

“Despite these continuing challenges for tapir conservation, most populations appear to be stable or increasing and the conservation outlook for the species is better than several decades ago, when the first efforts to protect the species began,” Kevin Flesher concludes.

Research article:

Flesher KM, Medici EP (2022) The distribution and conservation status of Tapirus terrestris in the South American Atlantic Forest. Neotropical Biology and Conservation 17(1): 1-19. https://doi.org/10.3897/neotropical.17.e71867

New rainfrog species named in honor of Greta Thunberg

The Rainforest Trust celebrated its 30th anniversary by hosting an auction offering naming rights for new-to-science species. The funds raised are to aid their conservation.

In 2018, Rainforest Trust celebrated its 30th anniversary by hosting an auction offering naming rights for some new-to-science species. The funds raised at the auction benefited the conservation of the newly recognized species. It is estimated that about 100 new species are discovered each year.

The scientific article officially describing and naming the new species, Pristimantis gretathunbergae, was published in Pensoft’s scientific journal ZooKeys.

Greta Thunberg, Sweden at the Annual Meeting 2019 of the World Economic Forum in Davos, January 25, 2019. Copyright by World Economic Forum / Manuel Lopez

The international team that discovered the new rainfrog was led by Abel Batista, Ph.D. (Panama) and Konrad Mebert, Ph.D. (Switzerland). The two have collaborated for 10 years in Panama and have published eight scientific articles together and described 12 new species.

  • Konrad Mebert. Photo by Abel Batista
  • Abel Batista. Photo by Konrad Mebert

The team found the frog on Mount Chucanti, a sky island surrounded by lowland tropical rainforest in eastern Panama. Reaching its habitat in the cloud forest required access via horseback through muddy trails, hiking up steep slopes, by-passing two helicopters that crashed decades ago, and camping above 1000 m elevation. The Chucanti reserve was established by the Panamanian conservation organization ADOPTA with support from Rainforest Trust.

Moments from the expedition. Photos by Konrad Mebert and Abel Batista

The Greta Thunberg Rainfrog exhibits distinctive black eyes—unique for Central American rainfrogs. Its closest relatives inhabit northwestern Colombia. Unfortunately, the frog’s remaining habitat is severely fragmented and highly threatened by rapid deforestation for plantations and cattle pasture. The Chucanti Reserve where the frog was first found is part of a growing network of natural parks and preserves championed by the Panamanian Government.

Greta Thunberg’s rainfrog, Pristimantis gretathunbergae. Photo by Konrad Mebert

The Rainforest Trust auction winner wanted to name the frog in honor of Greta Thunberg and her work in highlighting the urgency in preventing climate change. Her “School Strike for Climate” outside the Swedish parliament has inspired students worldwide to carry out similar strikes called Fridays for Future. She has impressed global leaders and her work is drawing others to action for the climate.

Greta Thunberg’s rainfrog, Pristimantis gretathunbergae. Photos by Konrad Mebert and Abel Batista

The plight of the Greta Thunberg Rainfrog is closely linked to climate warming, as rising temperatures would destroy its small mountain habitat. The Mount Chucanti region already has lost more than 30% of its forest cover over the past 10 years. Deadly chytrid fungus pose additional threats for its amphibians. Conservation of the remaining habitat is critical to ensure the survival of the frog. The important work in Panama by ADOPTA and Rainforest Trust globally to protect rainforests is critical to the survival of this frog and many other endangered species.

Research article:

Mebert K, González-Pinzón M, Miranda M, Griffith E, Vesely M, Schmid PL, Batista A (2022) A new rainfrog of the genus Pristimantis (Anura, Brachycephaloidea) from central and eastern Panama. ZooKeys 1081: 1–34. https://doi.org/10.3897/zookeys.1081.63009

First tarantula to live in bamboo stalks found in Thailand

A new genus of tarantula was discovered inside a bamboo culm from Mae Tho, Tak province, in Thailand. This is the first genus of tarantula that shows the surprising specialization of living in bamboo stalks. The bamboo culm tarantula Taksinus bambus was found in Thailand by JoCho Sippawat, a wildlife YouTuber from Thailand, who collaborated with arachnologists Dr. Narin Chomphuphuang and Mr. Chaowalit Songsangchote. The new genus and species are described in the journal ZooKeys.

Guest blog post by Dr. Narin Chomphuphuang

Bamboo is important to some animals as it can serve as a source of nutrition, shelter, and habitat. Inside a bamboo culm, we discovered a new genus of tarantula, which was collected from Mae Tho, Mueang Tak district, Tak province, in Thailand.

Mae Tho, Mueang Tak district, Tak province, in Thailand, where the newly described tarantula was discovered. Photo by Narin Chomphuphuang

The discovered genus has not been previously studied by scientists; this is the first case of a genus of tarantula that shows the surprising specialization of living in bamboo stalks.

The newly described tarantula Taksinus bambus seen in the bamboo stalk. Photo by JoCho Sippawat

We named the new tarantula genus Taksinus in honor of the Thai king Taksin the Great. The name was chosen in recognition of Taksin the Great’s old name, Phraya Tak – governor of Tak province, which is where the new genus was discovered. After the Second Fall of Ayutthaya in 1767, Taksin the Great was the only king of the Thonburi Kingdom to become a key leader of Siam, prior to the establishment of Thailand.

The bamboo culm tarantula Taksinus bambus was found in Thailand by JoCho Sippawat, a nationally known wildlife YouTuber in Thailand with 2.45 million subscribers, who collaborated with Dr. Narin Chomphuphuang and Mr. Chaowalit Songsangchote, the arachnologists who studied and described the new genus. 

Zongtum Sippawat, or JoCho Sippawat (left), with Wuttikrai Khaikaew, Kaweesak Keeratikiat, Narin Chomphuphuang and Chaowalit Songsangchote. Photo by Narin Chomphuphuang

In general, tarantulas from Southeast Asia can be either terrestrial or arboreal. Arboreal tarantulas spend time on different types of trees, but until now, researchers had not previously identified a tarantula found only on a specific tree type.

“These animals are truly remarkable; they are the first known tarantulas ever with a bamboo-based ecology,” Narin said.

Finding the new tarantula. Video by JoCho Sippawat

The tarantulas were discovered inside mature culms of Asian bamboo stalks (Gigantochloa sp.), with nest entrances ranging in size from 2–3 cm to a large fissure, within a silk-lined tubular burrow, either in the branch stub or in the middle of the bamboo culms. All the tarantulas found living in the culms had built silken retreat tubes that covered the stem cavity.

The tarantulas cannot bore into bamboo stems; therefore, they depend on the assistance of other animals. Bamboo is preyed upon by a variety of animals, including the bamboo borer beetle, bamboo worm, bamboo-nesting carpenter bee, and small mammals such as rodents. Furthermore, bamboo cracking is primarily caused by rapid changes in moisture content induced by the atmosphere, uneven drying, or drenching followed by rapid drying or by human activities. 

Taksinus bambus tarantula in its habitat. Photo by JoCho Sippawat

Taksinus is classified as a new genus within the Ornithoctoninae subfamily of Southeast Asian tarantulas. The discovery comes 104 years after Chamberlin defined the previous genus in this subfamily, Melognathus, in 1917.

What makes Taksinus distinct from all other Asian arboreal genera is the relatively short embolus of the male pedipalps, which is used to transport sperm to the female seminal receptacles during mating. In addition to morphology, its habitat type and distribution are also different from those of related species. While Asian arboreal tarantulas have been reported in Indonesia (Sangihe Island and Sulawesi), Malaysia, Singapore, Sumatra, and Borneo, Taksinus was discovered in northern Thailand, which is a new geographical location for those spiders.

Looking at an entrance hole of a bamboo culm tarantula. Photo by Narin Chomphuphuang

“We examined all of the trees in the area where the species was discovered. This species is unique because it is associated with bamboo, and we have never observed this tarantula species in any other plant. Bamboo is important to this tarantula, not only in terms of lifestyle but also because it can only be found in high hill forests in the northern part of Thailand, at an elevation of about 1,000 m. It is not an exaggeration to say that they are now Thailand’s rarest tarantulas,” says Narin.

The tarantula Taksinus bambus in its habitat. Photo by JoCho Sippawat

Few people realize how much of Thailand’s wildlife remains undocumented. Thai forests now cover only 31.64% of the country’s total land area. We are primarily on a mission to research and save the biodiversity and wildlife within these forests from extinction, especially species-specific microhabitats.

Research article:

Songsangchote C, Sippawat Z, Khaikaew W, Chomphuphuang N (2022) A new genus of bamboo culm tarantula from Thailand (Araneae, Mygalomorphae, Theraphosidae). ZooKeys 1080: 1-19. https://doi.org/10.3897/zookeys.1080.76876

Extensive practical guide to DNA-based biodiversity assessment methods published as a ‘living’ document by DNAqua-Net COST Action

Between 2016 and 2021, over 500 researchers collaborated within the DNAqua-Net international network, funded by the European Union’s European Cooperation in Science and Technology programme (COST), with the goal to develop and advance biodiversity assessment methods based on analysis of DNA obtained from the environment (e.g. river water) or from unsorted collections of organisms. 

Such innovative methods are a real game changer when it comes to large-scale assessment of biodiversity and ecological monitoring, as collecting environmental samples that are sent to the lab for analysis is much cheaper, faster and non-invasive, compared with capturing and examining live organisms. However, large-scale adoption has been hindered by a lack of standardisation and official guidance. 

Recognising the urgent need to scale up ecological monitoring as we respond to the biodiversity and climate crises, the DNAqua-Net team published a guidance document for the implementation of DNA-based biomonitoring tools.

The guide considers four different types of samples: water, sediments, invertebrate collections and diatoms, and two primary analysis types: single species detection via qPCR and similar targeted methods; and assessment of biological communities via DNA metabarcoding. At each stage of the field and laboratory process the guide sets out the scientific consensus, as well as the choices that need to be made and the trade-offs they entail. In particular, the guide considers how the choices may be influenced by common practical constraints such as logistics, time and budget. Available in an Advanced Book format, the guidelines will be updated as the technology continues to evolve.

Leaders of DNAqua-Net are Prof. Dr. Florian Leese of the University of Duisburg-Essen (Germany) and Dr. Agnès Bouchez of the French National Institute for Agriculture, Food, and Environment (INRAE). The core writing team for the present guide book involves Dr. Micaela Hellström (MIX Research AB, Sweden), Dr. Kat Bruce (NatureMetrics Ltd., UK), Dr. Rosetta Blackman (University of Zurich and EAWAG, Switzerland), Dr. Sarah Bourlat (LIB/Museum Koenig, Germany), and Prof. Kristy Deiner (ETH Zurich and SimplexDNA AG, Switzerland).

“Back in 2016 we realised that all around the globe researchers are testing new eDNA methods, developing individual solutions and products. While this is excellent, we need to reach a consensus and provide this consensus to stakeholders from the applied sectors”, 

says Florian Leese.
This video was created as part of EU COST Action DNAqua-Net (CA15219) and shows how environmental DNA (eDNA) can be sampled and analysed from aquatic ecosystems. It shows the whole cycle from the start to final results. 
Credit: DNAqua-Net

The guide’s lead author Dr. Kat Bruce adds:

“The urgency of addressing the twin biodiversity and climate crises means that we need to accelerate the adoption of new technologies that can provide data and insights at large scales. In doing so, we walk a tricky line to agree on sufficiently standardised methods that can be usefully applied as soon as they add value, while still continuing to develop them further and innovate within the field. It was a daunting task to seek consensus from several hundred scientists working in a fast-moving field, but we found that our technology is based on a strong foundation of knowledge and there was a high level of agreement on the core principles – even if the details vary and different users make different choices depending on their environmental, financial or logistical constraints.”

Looking back on the last four years that culminated in the publication of a “living” research publication, Prof. Dr. Kristy Deiner says:

“The document took many twists and turns through more than ten versions and passionate discussions across many workshops and late night drinks. All in the days when we could linger at conferences without fear of the pandemic weighing on us. As we worked to find consensus, one thing was clear: we had a lot to say and a standard review paper was not going to cut it. With the knowledge and experience gathered across the DNAqua-Net, it made sense to not limit this flow of information, but rather to try and tackle it head on and use it to address the many questions we’ve all struggled with while developing DNA-based biodiversity survey methods.”

Now that the document – or at least its first version – is publicly available, the researchers are already planning for the next steps and challenges.

“The bottom line is we’ve come a long way in the last ten years. We have a buffet of methods for which many produce accurate, reliable and actionable data to the aid of biodiversity monitoring and conservation. While there is still much work to be done, the many unanswered questions are because the uptake is so broad. With this broad uptake comes novel challenges, but also new insights and a diversity of minds with new ideas to address them. As said this is planned to be a living document and we welcome continued inputs no matter how great or small,” says Deiner.

Dr. Micaela Hellström recalls:

“The book evolved over the four years of COST Action DNAqua-Net which made it possible for the many scientists and stakeholders involved to collaborate and exchange knowledge on an unprecedented scale. Our whole team is well aware of the urgent need to monitor biodiversity loss and to provide accurate species distribution information on large scales, to protect the species that are left. This was a strong driving force for all of us involved in the production of this document. We need consensus on how to coherently collect biodiversity data to fully understand changes in nature.”

“It was a great and intense experience to be a part of the five-person core writing team. In the months prior to submitting the document, we spent countless hours, weekends and late nights researching the field, communicating with researchers and stakeholders, and joining vivid Zoom discussions. As a result, the present book provides solid guidance on multiple eDNA monitoring methods that are – or will soon become – available as the field moves forward.” 

***

The DNAqua-Net team invites fellow researchers and practitioners to provide their feedback and personal contributions using the contacts below.

***

Original source:

Bruce K, Blackman R, Bourlat SJ, Hellström AM, Bakker J, Bista I, Bohmann K, Bouchez A, Brys R, Clark K, Elbrecht V, Fazi S, Fonseca V, Hänfling B, Leese F, Mächler E, Mahon AR, Meissner K, Panksep K, Pawlowski J, Schmidt Yáñez P, Seymour M, Thalinger B, Valentini A, Woodcock P, Traugott M, Vasselon V, Deiner K (2021) A practical guide to DNA-based methods for biodiversity assessment. Advanced Books. https://doi.org/10.3897/ab.e68634

Accidental tree wound reveals novel symbiotic behavior

Despite significant movement restrictions during the first wave of the pandemic in Panama City, a group of curious high school students roamed their neighborhood drilling holes into Cecropia trees and documenting how Azteca alfari ants responded to damage to their host plant.

During the pandemic, five curious high school students accidentally discovered how Azteca alfari ants respond to damage to their Cecropia host trees. Photo by Donna Conlon

One afternoon, during the early days of the COVID-19 pandemic in Panama, a bored teenager with a slingshot and a clay ball accidentally shot entry and exit holes in a Cecropia tree trunk. These are “ant-plant” trees, which famously cooperate with fierce Azteca ants; the trees provide shelter and food to the ants, and in exchange the ants defend their leaves against herbivores. The next morning, to his surprise, the Azteca alfari ants living within the Cecropia trunk had patched up the wound.

This unexpected occurrence drove five curious high school students, with time on their hands, to participate in the Smithsonian Tropical Research Institute’s (STRI) volunteer program, and they enlisted STRI scientist William T. Wcislo’s help in devising their experiment. Despite significant movement restrictions during the first wave of the pandemic, they roamed their neighborhood drilling holes into Cecropia trees and documenting the ants’ responses to the damage.

They found that as soon as the plants had holes drilled into them, the ants ran to the wound area and began patching it up. Within 2.5 hours, the size of the hole had been significantly reduced and it was often completely repaired within 24 hours.

Although some Azteca ants are known to defend their Cecropia host plants against herbivores, these new results, published in the Journal of Hymenoptera Research, reveal that not only do the ants behave in ways to minimize damage to their hosts, but when damage does occur, they actively work to fix it, particularly when their brood is directly threatened.

“I was totally surprised by the results,” says William Wcislo. “And I was impressed by how they developed a simple way to test the idea that ants repair damage to their home.” 

Azteca ant and Cecropia plant responses to wounds in the stems a a sealed hole after 24 hours, but not yet filled in to the stem surface (arrow) b a fully patched and filled-in hole after 24 hrs, oozing sap from the ant-sealed wound (arrow) c a natural plant scar surrounding a 6.4 mm hole that was fully sealed by the ants, approximately 5 months later d a hole in a plant without ants after 24 hrs, showing the green wall of the opposite side of the stem (arrow).

Sloths and silky anteaters often visit Cecropia trees and their sharp toenails sometimes pierce the wood, so the researchers speculate that these occurrences, which are far more common and ancient threats to the Cecropia than teenagers shooting clay balls at them, could have led Azteca alfari ants to evolve the observed repair behavior when their host plant is damaged. 

Their experiment also left them with new questions, since not all of the ant colonies repaired the damage to their host plants. Understanding what factors influence the ants to take action could be the subject of future research for these budding scientists, although perhaps to be addressed after graduating from high school.

“Sometimes messing around with a slingshot has a good outcome,” said lead author Alex Wcislo. “This project allowed us to experience first-hand all the intricacies behind a scientific study. All in all, it was a great learning experience, especially considering the difficulties associated with fulfilling this due to COVID-19.”

Research article:

Wcislo A, Graham X, Stevens S, Toppe JE, Wcislo L, Wcislo WT (2021) Azteca ants repair damage to their Cecropia host plants. Journal of Hymenoptera Research 88: 61-70. https://doi.org/10.3897/jhr.88.75855

The tallest begonia species in all Asia found in Tibet, China

Chinese researchers have discovered the tallest Begonia recorded in Asia. The plant belongs to a new species aptly called Begonia giganticaulis.

With over 2050 known species, Begonia is one of the largest plant genera. Since most begonias are small weeds, a begonia taller than a human is a very unusual sight. However, the newly discovered Begonia giganticaulis is one of the few exceptions.

Flowers of Begonia giganticaulis.

In 2019, Dr. Daike Tian and his colleagues initiated a field survey on wild begonias in Tibet, China. On September 10, 2020, when Dr. Tian saw a huge begonia in full bloom during surveys in the county of Mêdog, he got instantly excited. After checking its flowers, he was confident it represented a new species.

  • Dr. Daike Tian with an individual of Begonia giganticaulis. Photo by Qing-Gong Mao
  • The research team measures the height of a Begonia giganticaulis individual at its collection site. Photo by Qing-Gong Mao

From a small population with a few dozens of individuals, Dr. Tian collected two of the tallest ones to measure them and prepare specimens necessary for further study. One of them was 3.6 meters tall, the thickest part of its ground stem close to 12 cm in diameter. To measure it correctly, he had to ask the driver to stand on top of the vehicle. In order to carry them back to Shanghai and prepare dry specimens, Dr. Tian had to cut each plant into four sections.

A Begonia giganticaulis plant is cut up for easier transportation
A Begonia giganticaulis plant is cut up for easier transportation. Photo by Daike Tian

To date, this plant is the tallest begonia recorded in the whole of Asia.

Begonia giganticaulis, recently described as a new species in the peer-reviewed journal PhytoKeys, grows on slopes under forests along streams at elevation of 450–1400 m. It is fragmentally distributed in southern Tibet, which was one of the reasons that its conservation status was assigned to Endangered according to the IUCN Red List Categories and Criteria.

The research team pose with a specimen of Begonia giganticaulis at the first Chinese begonia show in Shanghai Chenshan Botanical Garden.
The research team pose with a specimen of Begonia giganticaulis at the first Chinese begonia show in Shanghai Chenshan Botanical Garden. Photo by Meiqin Zhu

After being dried at a herbarium and mounted on a large board, the dried specimen was measured at 3.1 m tall and 2.5 m wide. To our knowledge, this is the world’s largest specimen of a Begonia species. In October 2020, the visitors who saw it at the first Chinese begonia show in Shanghai Chenshan Botanical Garden were shocked by its huge size.

Currently, the staff of Chenshan Herbarium is applying for Guinness World Records for this specimen.

Research article:

Tian D-K, Wang W-G, Dong L-N, Xiao Y, Zheng M-M, Ge B-J (2021) A new species (Begonia giganticaulis) of Begoniaceae from southern Xizang (Tibet) of China. PhytoKeys 187: 189-205.https://doi.org/10.3897/phytokeys.187.75854

A year of biodiversity: Top 10 new species of 2021 from Pensoft journals, Part 2

While 2021 may have been a stressful and, frankly, strange year, in the world of biodiversity there has been plenty to celebrate! Out of the many new species we published in our journals this year, we’ve curated a selection of the 10 most spectacular discoveries. The world hides amazing creatures just waiting to be found – and we’re making this happen, one new species at a time.

Read Part 1 of the Top 10 new species of 2021 here.

5. The Instagram model

Many students and young researchers are encouraged to explore biodiversity by starting from their own backyard. Yes, but how often do they find undescribed snake species in there?

This is exactly what happened to Virendar K. Bhardwaj, a master student in Guru Nanak Dev University in Amritsar. Confined to his home in Chamba, India because of the COVID-19 lockdown, he started photographing any wildlife he came across and uploading it on his Instagram account. One of his images showed a beautiful kukri snake.

The picture immediately caught the attention of Zeeshan A. Mirza (National Centre for Biological Sciences, Bangalore) and Harshil Patel (Veer Narmad South Gujarat University, Surat), who worked together with Virendar to describe it as a new species under the name Oligodon churahensis.

“It is quite interesting to see how an image on Instagram led to the discovery of such a pretty snake that, until very recently, remained hidden to the world,” Zeeshan A. Mirza told us earlier this month.

“What’s even more interesting is that the exploration of your own backyard may yield still undocumented species. Lately, people have been eager to travel to remote biodiversity hotspots to find new or rare species, but if one looks in their own backyard, they may end up finding a new species right there.”

Published in: Evolutionary Systematics

4. The tiny snail with an athletic name

Do freshwater snails make good tennis players? Well, one of them certainly has the name for it.

Enter Travunijana djokovici, a new species of aquatic snail named after famous Serbian ten­nis player Novak Djokovic.

Found in a karstic spring near Podgorica, the capital of Montenegro, T. Djokovici is part of the family of mud snails, which inhabit fresh or brackish water, including caves and subterranean habitats.

The tiny snail was discovered by Slovak biospeleologist Jozef Grego and Montenegrin zoologist Vladimir Pešić of the University of Montenegro, who claim they named it after the renowned tennis player “to acknowledge his inspiring enthusiasm and energy.”.

To discover some of the world’s rarest animals that inhabit the unique underground habitats of the Dinaric karst, to reach inaccessible cave and spring habitats and for the restless work during processing of the collected material, you need Novak’s energy and enthusiasm,” they add.

Amazingly, Novak Djokovic found out that he’s now a namesake to a tiny snail, and he even had a comment.

“I am honoured that a new species of snail was named after me because I am a big fan of nature and ecosystems and I appreciate all kinds of animals and plants,” he says in an Eurosport article. “I don’t know how symbolic this is, because throughout my career I always tried to be fast and then a snail was named after me,” he joked. “Maybe it’s a message for me, telling me to slow down a bit!”

Published in: Subterranean Biology

3. The Coronavirus caddisfly

The COVID-19 pandemic has undoubtedly affected all of us, and the scientific world is no exception. Fieldwork got postponed, museums remained closed, arranging meet-ups and travel became almost impossible.

Scientists used this as a drive and inspiration as they continued their hard work on new discoveries. Only this year, we published the descriptions of the beetle Trigonopterus corona, the wasp Allorhogas quarentenus, and, yes, the caddisfly Potamophylax coronavirus.

P. coronavirus was collected near a stream in the Bjeshkët e Nemuna National Park in Kosovo by a team of scientists led by Professor Halil Ibrahimi of the University of Prishtina. After molecular and morphological analyses, it was described as a caddisfly species new to science. Its name will be an eternal memory of an extremely difficult period.

In a broader sense, the researchers also wish to bring attention to “another silent pandemic occurring on freshwater organisms in Kosovo’s rivers,” caused by the pollution and degradation of freshwater habitats, as well as the activity increasing in recent years of mismanaged hydropower plants. Particularly, the river basin of the Lumbardhi i Deçanit River, where the new species was discovered, has turned into a ‘battlefield’ for scientists and civil society on one side and the management of the hydropower plant operating on this river on the other.

P. coronavirus is part of the small insect order of Trichoptera, which is very sensitive to water pollution and habitat deterioration. The authors of the species argue that it is a small-scale endemic taxon, very sensitive to the ongoing activities in Lumbardhi i Deçanit river, and failure to understand this may drive it, along with many other species, towards extinction.

Published in: Biodiversity Data Journal

2. The cutest peacock spider ever

If you think spiders can’t be cute, you’ve probably never seen a peacock spider. They have big forward-facing eyes, and their males perform fun courtship dances.

Citizen scientist Sheryl Holliday was the first to spot this vibrant spider while walking in Mount Gambier, Australia, and she posted her find on Facebook. It was later described as a new species by arachnologist Joseph Schubert of Museums Victoria.

Coloured bright orange, it was called Maratus Nemo, after the popular Disney character.

‘It has a really vibrant orange face with white stripes on it, which kind of looks like a clown fish, so I thought Nemo would be a really suitable name for it,’ Joseph Schubert says.

Maratus Nemo is probably the first influencer arachnid – his curious story, bright colours and fun name practically made him an internet star overnight.

Published in: Evolutionary Systematics

1. The tiny ant that challenges gender stereotypes

Found in Ecuador’s evergreen tropical forests, this miniature trap jaw ant bears the curious Latin name Strumigenys ayersthey. Unlike most species named in honour of people, whose names end with -ae (after females) and –i (after males), S. ayersthey might be the only species in the world to have a scientific name with the suffix –they.

“In contrast to the traditional naming practices that identify individuals as one of two distinct genders, we have chosen a non-Latinized portmanteau honoring the artist Jeremy Ayers and representing people that do not identify with conventional binary gender assignments, Strumigenys ayersthey,” authors Philipp Hoenle of the Technical University of
Darmstadt and Douglas Booher of Yale University state in their paper.

“Strumigenys ayersthey sp. nov. is thus inclusively named in honor of Jeremy Ayers for the multitude of humans among the spectrum of gender who have been unrepresented under traditional naming practices.”

Curiously, it was no other than lead singer and lyricist of the American alternative rock band R.E.M. Michael Stipe that joined Booher in writing the etymology section for the research article, where they explain the origin of the species name and honor their mutual friend, activist and artist Jeremy Ayers.

This ant can be distinguished by its predominantly smooth and shining cuticle surface and long trap-jaw mandibles, which make it unique among nearly a thousand species of its genus.

“Such a beautiful and rare animal was just the species to celebrate both biological and human diversity,” Douglas Booher said.

Published in: ZooKeys

Scientists discover White-handed gibbons that have been evolving in the south of Malaysia

Genetic assessment of captive gibbons to identify their species and subspecies is an important step before any conservation actions. A group of wildlife researchers recently discovered a previously unknown population of white-handed gibbons (subspecies lar) from Peninsular Malaysia. Their findings are now published in the open-access journal ZooKeys. Betsy and Lola are among the captive white-handed gibbons undergoing a strict rehabilitation process before being released back to the wild.

Many captive gibbons kept in zoos and rescue centres have been seized from illegal pet trade, private collectors, and plantations where their natural habitats are getting destroyed. 

In 2013, the National Wildlife Rescue Centre (NWRC) of the Department of Wildlife and National Parks (PERHILITAN) was established in Peninsular Malaysia to help with the rehabilitation of wildlife species – including gibbons – before they are reintroduced or translocated back to the wild. Under the Primate Rehabilitation Programme initiated by PERHILITAN, captive gibbons have to go through a number of procedures and assessments, where their taxonomy and genetics might be examined, before they can go back to living in the wild.

Members of the research team at National Wildlife Forensic Laboratory of DWNP. Photo by PERHILITAN

Following the Guidelines for Reintroductions and Other Conservation Translocations provided by the IUCN Species Survival Commission, researchers Dr Jeffrine J. Rovie-Ryan from Universiti Malaysia Sarawak and Millawati Gani and colleagues from the National Wildlife Forensic Laboratory of PERHILITAN conducted a genetic assessment on 12 captive white-handed gibbons in NWRC. Determining the subspecies and origin of the animals is an important step that informs further decisions on their translocation and reintroduction.

In a research paper published in the open-access journal ZooKeys, the team describes a previously unknown southern population of the white-handed gibbon subspecies lar living in Peninsular Malaysia. In what started as a straightforward species and subspecies identification process using DNA technology, the researchers discovered unusual mutations in the DNA of the studied gibbons. This is how the researchers found themselves before a distinct population, which they concluded must have been evolving in isolation.

Lola (left) and Betsy (right), two of the White-handed gibbons of the Hylobates lar lar subspecies undergoing rehabilitation process at Pulau Ungka, NWRC. Photo by Hani Nabilia and PERHILITAN

“Given the prolonged isolation, it is likely that the southern population has undergone some local speciation, but this finding should be regarded as preliminary and requires further investigation,” explained Dr Jeffrine. Furthermore, the researchers suggest there might be a northern population inhabiting Southern Thailand.

Still going through rehabilitation, the gibbons from the study have been pre-released into a semi-wild enclosure known as Pulau Ungka (Gibbon Island), where their recovery is closely monitored by primate experts of PERHILITAN.

Research article:

Gani M, Rovie-Ryan JJ, Sitam FT, Mohd Kulaimi, NA, Zheng, CC, Atiqah AN, Abd Rahim, NM, Mohammed AA (2021) Taxonomic and genetic assessment of captive White-Handed Gibbons (Hylobates lar) in Peninsular Malaysia with implications towards conservation translocation and reintroduction programme. ZooKeys 1076: 25–41 (2021), doi: 10.3897/zookeys.1076.73262

A year of biodiversity: Top 10 new species of 2021 from Pensoft journals, Part 1

With 2022 round the corner, we thought we’d start off the celebrations by looking back to some the most memorable discoveries of 2021. And what a year it has been! Many new species made their debuts on the pages of Pensoft journals – here’s our selection of the most exciting animals, plants and fungi that we published in 2021.

With 2022 round the corner, we thought we’d start off the celebrations by looking back to some the most memorable discoveries of 2021. And what a year it has been! Many new species made their debuts on the pages of Pensoft journals – here’s our selection of the most exciting animals, plants and fungi that we published in 2021.

10. The delicious wild oak mushroom

It’s amazing that edible species, long known to local communities, can still present a novelty for science. This was the case with Cantharellus veraecrucis, a chanterelle from – that’s right, Veracruz, Mexico.

During the rainy season, locals harvest this mushroom from tropical oak forests to sell it or enjoy it as a delicacy; this is probably why they’ve dubbed it “Oak mushroom”.

Published in: MycoKeys

9. The master of disguise

If you ever see a leaf insect, there’s a good chance you won’t notice it – these little critters are masters of camouflaging.

This picture was taken in 2014, when Jérôme Constant and Joachim Bresseel from the Royal Belgian Institute of Natural Sciences were enjoying a night walk in Vietnam’s Nui Chua National Park. It wasn’t until this year, though, that this beauty got its own scientific name: Cryptophyllium nuichuaense. Named after the park where it was found, it is one of 13 new species of leaf insects described in our journal ZooKeys this February.

This leaf insect, like many others, is endemic to Vietnam. This is why the researchers who found itcall for the creation of more protected areas in order to keep this precious biodiversity intact.

Published in: ZooKeys

8. The Neil Gaiman spider

Unlike most spiders, trapdoor spiders don’t use silk to make a web. Instead, they live in burrows lined with silk that they cover with a “trapdoor”. They are relatively widely spread, but you’d rarely encounter one out in the open, because they spend most of their lives underground.

This is probably why arachnologists and spider lovers the world over got so excited when Dr. Rebecca Godwin (Piedmont University, GA) and Dr. Jason Bond (University of California, Davis, CA) described 33 new species of trapdoor spiders from the genus Ummidia – in addition to the 27 already known.

Dr. Rebecca Godwin talks to L. Brian Patrick about her discovery of 33 new species of trapdoor spiders on his podcast New Species.

One of the 33 is Ummidia neilgaimani, named after fantasy and horror writer Neil Gaiman. A particular favorite of Dr. Godwin, Gaiman is the author of a number of books with spider-based characters. His novel American Gods features a character based on the West African spider god Anansi and a World Tree “one hour south of Blacksburg,” not far from the type locality of this species. He’s also part of the documentary Sixteen Legs, in his own words “An amazing film about Tasmanian cave spider sex.”

“I think anything we can do to increase people’s interest in the diversity around them is worthwhile and giving species names that people recognize but that still have relevant meaning is one way to do that,” says Dr. Godwin.

Published in: ZooKeys

7. The deadly Chinese-goddess snake

Bungarus suzhenae was only described as a new species this year, but its reputation preceded it – in a bad way. Researchers were already familiar with a notorious black-and-white banded krait that bit herpetologists on expeditions in Myanmar and China – in one infamous case, to death. After extensive morphological and phylogenetical analysis, the researchers were finally able to confirm it as new to science.

The story behind B. suzhenae’s name is interesting, too: it was named after a character from the traditional Chinese myth ‘Legend of White Snake’. The powerful snake goddess Bai Su Zhen is to this day regarded as a symbol of true love and good-heartedness in China. 

Snakebites from kraits – including this one – are known to have a high mortality. This is why the new knowledge on B. suzhenae and its description as a new species are essential to the research on its venom and an important step in the development of antivenom and improved snakebite treatment.

Published in: ZooKeys

6. The ephemeral fairy lanterns

Commonly known as “fairy lanterns”, plants of the genus Thismia are very rare and small in size. They are mycoheterotrophic, which means they live in close association with fungi from which they acquire most of their nutrition. They’re also very elusive, growing in dark, remote rainforests, and visible only when they emerge to flower and set seed after heavy rain.

In fact, researchers were only able to find one specimen of the new T. sitimeriamiae, which they discovered in the Terengganu State of Malaysia – the rest of the population had been destroyed by wild boars.

Just discovered, T. sitimeriamiae may already be threatened by extinction – which is why the research team that discovered it suggest that this exceptionally rare plant is classified as Critically Endangered.

Published in: PhytoKeys

A year of biodiversity: Top 10 new species of 2021 from Pensoft journals, Part 2