Ants Recognize Infected Wounds and Treat Them

A Matabele ant tends to the wound of a fellow ant whose legs were bitten off in a fight with termites.
 Photo Credit: Erik Frank / Universität Würzburg

The African Matabele ants are often injured in fights with termites. Their conspecifics recognize when the wounds become infected and initiate antibiotic treatment.

The Matabele ants (Megaponera analis), which are widespread south of the Sahara, have a narrow diet: They only eat termites. Their hunting expeditions are dangerous because termite soldiers defend their conspecifics – and use their powerful mandibles to do so. It is therefore common for ants to be injured while hunting.

If the wounds become infected, there is a significant survival risk. However, Matabele ants have developed a sophisticated healthcare system: they can distinguish between non-infected and infected wounds and treat the latter efficiently with antibiotics they produce themselves. This is reported by a team led by Dr Erik Frank from Julius-Maximilians-Universität (JMU) Würzburg and Professor Laurent Keller from the University of Lausanne in the journal Nature Communications.

Human-driven extinction of birds much greater than previously known

The dodo was endemic to the island of Mauritius. It could not fly and was exterminated by man during the 17th century.
Image Credit: German Rojas

On many of the world's islands, bird species began to become extinct with the arrival of humans. In a new study involving researchers from the University of Gothenburg and Uppsala University, it is estimated that humans have contributed to the extinction of around 1,400 bird species – twice as high as previously thought.

Because the lightweight bones of birds break down quickly, few fossils are formed. In the past, when scientists had to rely on observations and fossils, it was estimated that 640 species of birds had become extinct during the lifetime of modern humans, 90 percent of them on islands inhabited by humans. Classic examples are the dodo on Mauritius and the great auk in the North Atlantic, which, like penguins, could not fly.

However, by using statistical modeling, scientists now dare to estimate that around 1,400 bird species have become extinct.

“This is twice as many species as those that have left fossils as evidence of their existence. “Virtually all of these species were wiped out directly or indirectly due to human activity,” says Søren Faurby, a researcher in Zoology at the University of Gothenburg and co-author of the study published in Nature Communications.

Insects already had a variety of defense strategies in the Cretaceous

Larva of a wedge-shaped beetle in amber, which could have lived inside other insects like its modern counterparts. 
Image Credit: © Carolin Haug

Analyses of amber show that insect larvae were already using a wide variety of tactics to protect themselves from predators 100 million years ago.

Early life stages of insects fulfill important functions in our ecosystems. They decompose dead bodies and wood, forming soil and returning various elements into material cycles. Not least, they are a major food source for many larger animals such as birds and mammals. This has led to many insect larvae developing structures and strategies for reducing the danger of being eaten. These include features like spines and hairs, but also camouflage and concealment. Over millions of years, a wide variety of such adaptation strategies have developed.

Researchers at LMU and the universities of Greifswald and Rostock have studied particularly well-preserved fossils from Burmese amber and have been able to demonstrate that such anti-predator mechanisms had already evolved very diverse forms in insect larvae during the Cretaceous period 100 million years ago. This includes well-known strategies such as that employed by lacewing larvae, which carry various plant and animal materials on their back to give them camouflage, or the ploy of mimicking the appearance of certain plant parts.

Scientists collect aardvark poop to understand how the species is impacted by climate in Africa

Aardvark.
Photo Credit: Peter Buss

In a first-of-its-kind study of aardvarks, Oregon State University researchers spent months in sub-Saharan Africa collecting poop from the animal and concluded that aridification of the landscape is isolating them, which they say could have implications for their long-term survival.

“Everyone had heard of aardvarks and they are considered very ecologically important but there has been little study of them,” said Clint Epps, a wildlife biologist at Oregon State. “We wanted to see if we could collect enough data to begin to understand them.”

In a just-published paper in Diversity and Distribution, the researchers used genetic information gleaned from 104 aardvark poop samples to begin to understand the range of where they live.

“During times of rapid environmental change, evaluating and describing changes in the landscape where a species lives is important for informed conservation and management decisions,” said Rachel Crowhurst, a wildlife geneticist who works with Epps and co-authored the paper.

Deadly chicken disease: ancient DNA reveals evolution of virulence

With the increase in poultry farming, Marek's disease virus evolved
Photo Credit: Heidi-Ann Fourkiller

Using genetic analyses, an international team led by LMU paleogeneticist Laurent Frantz has revealed the evolutionary history of the pathogen of a fatal disease in chickens.

A notifiable animal disease in Germany, Marek’s disease is caused by the globally distributed Marek’s disease virus (MDV). Over the past century, the virus, which causes tumors in chickens and has a high mortality rate, has become increasingly aggressive. Combating the disease costs the poultry industry over a billion dollars every year. With the help of ancient DNA, an international team of scientists led by LMU paleogenomicist Professor Laurent Frantz and Professor Greger Larson and Professor Adrian Smith from the University of Oxford has now decoded the evolution of MDV and shed light on what is behind the growing virulence.

The international team from the fields of paleogenetics, archeology, and biology isolated viral genomes from chicken bones up to 1,000 years old from 140 archeological sites in Europe and the Near East. “Our data shows that the virus was already widely distributed at least 1,000 years before the first description of the disease in 1907,” says Frantz. When the disease was first described, it was said to produce only mild symptoms in older chickens. With the dramatic increase in poultry farming in the 1950s and 1960s, the virus evolved and has become increasingly virulent despite the development of several vaccines.

Camera traps uncover mysterious lesula monkey’s ‘business’

Camera traps equipped with infrared sensors automatically and non-invasively captured videos of Africa’s lesula monkey in the central Congo Basin in the Democratic Republic of the Congo without any disturbance to their social groups.

Video Credit: Florida Atlantic University

Strategically placed camera traps have uncovered the mysterious behavior of an elusive species of African monkey – Cercopithecus lomamiensis, commonly known as the “lesula.”

In much the same way that Ring home security cameras capture both mundane and extraordinary events, strategically placed camera traps have uncovered the mysterious behavior of an elusive species of African monkey – Cercopithecus lomamiensis, commonly known as the “lesula.” With its large human-like eyes, golden mane and pink face, this cryptic species was discovered in 2012 in the central Congo Basin in the Democratic Republic of the Congo.

Because of the lesula’s mysterious behavior, traditional observational methods in the field are challenging. To date, no behavioral study has been done to evaluate this species’ degree of terrestriality.

To address a lack of comprehensive ecological knowledge on this lineage, Florida Atlantic University researchers were the first to design and employ an intensive camera trap study to document the lesula’s terrestrial movement, daytime activity pattern, birth seasonality, group size and social organization.

Camera traps, equipped with infrared sensors to automatically and non-invasively capture videos, provided the researchers with the best approach to estimate group counts from non-habituated lesula individuals without any disturbance to their social groups.

Bats declined as Britain felled trees for colonial shipbuilding

A western barbastelle.
Photo Credit: Antton Alberdi

Bat numbers declined as Britain’s trees were felled for shipbuilding in the early colonial period, new research shows.

The study, by the University of Exeter and the Bat Conservation Trust (BCT), found Britain’s Western barbastelle bat populations have dropped by 99% over several hundred years.

Animals’ DNA can be analyzed to discover a “signature” of the past, including periods when populations declined, leading to more inbreeding and less genetic diversity.

Scientists used this method to discover the historic decline of Western barbastelles in Britain – and also analyzed modern landscapes to see what helps and harms bats.

They found more genetic diversity among bats in areas rich in broadleaf woodland and diverse habitats.

Artificial light reduced connectivity between populations, probably because bats avoid areas with bright lighting, while rivers and woodlands increased connectivity.

“These bats usually roost in mature oak and beech trees, and move around every few nights – so they benefit from areas with substantial woodland cover,” said Dr Orly Razgour, from the University of Exeter.

Poison dart frogs: Personality determines reproductive strategies

The Allobates femoralis species of poison dart frogs follows different strategies during reproduction according to their behavioral type.
Photo Credit: Eva Ringler

Poison frogs of the species Allobates femoralis are common in the rainforests in South America. Their highly poisonous relatives, such as frogs of the genus Phyllobates, were frequently used by indigenous people of Colombia to extract toxins by rubbing the skin onto arrowheads for the purposes of hunting and fighting. Allobates femoralis frogs are not poisonous. Like many other animal species, however, they have distinct personality traits. Both the males and females, for example, may be particularly bold, aggressive, or eager to explore. Poison frogs mate with several partners over the course of a reproductive period and their character traits have a considerable influence on the reproductive strategies employed by individual animals. 

Most of the previous studies in other animal taxa have examined the effect of personality traits on a single measure of reproductive success. In two recently published studies, researchers in the Institute of Ecology and Evolution at the University of Bern have presented new results on the effects of different combinations of personality traits in both males and females on different components of reproductive success. They examined the influence of personality on mating success, the number of clutches produced, as well as the numbers of offspring that survive into adulthood. The researchers were able to show that certain personality traits are already present in poison dart frogs at tadpole stage and that they also persist after the subsequent metamorphosis. 

Why are songbirds larger in colder climates?

A song-sparrow
Photo Credit: Anish Lakkapragada

Scientists have unlocked the genetic basis underlying the remarkable variation in body size observed in song sparrows, one of North America’s most familiar and beloved songbirds. This discovery also provides insights into this species’ capacity to adapt to the challenges of climate change.

The study, published today in Nature Communications, used genomic sequencing to successfully pinpoint eight genetic variants, or DNA mutations, largely responsible for the nearly threefold difference in body size observed across the song sparrow range from Mexico to Alaska. For instance, song sparrows that live year-round in the Aleutian Islands can be up to three times larger than their counterparts in the coastal marshes of California.

Katherine Carbeck, the study’s first author and a PhD candidate in the faculty of forestry, University of British Columbia, explains that body size varies predictably in many species that inhabit vastly different climatic conditions, aligning with “Bergmann’s rule” which states that organisms in cooler climates tend to be larger as an adaptation to regulate body temperature.

European wildcats avoided introduced domestic cats for 2000 years

A wildcat which is part of the Saving Wildcats conservation breeding for release program which conducted the first release of wildcats to the Cairngorms National Park, Scotland in 2023
Photo Credit: Saving Wildcats

Domestic cats introduced from the Near East and wildcats native to Europe did not mix until the 1960s, despite being exposed to each other for two thousand years.

Two studies published today in Current Biology involving new archaeological and genetic evidence rewrites the history of cats in Europe.

The international team of researchers sequenced and analyzed both wildcats and domestic cats including 48 modern individuals and 258 ancient samples excavated from 85 archaeological sites over the last 8,500 years. They then assessed the patterns of hybridization (or interbreeding) after domestic cats were introduced to Europe over 2,000 years ago, and came into contact with native European wildcats.

The results of the studies demonstrate that, since their introduction, domestic cats and European wildcats generally avoided mating with each other. About 50 years ago in Scotland, however, that all changed and rates of interbreeding between wildcats and domestic cats rose rapidly. This may have happened as a result of dwindling wildcat populations and a lack of opportunity to mate with other wildcats.

Study reveals location of starfish’s head

Postdoctoral scholar Laurent Formery (left) and biology Professor Christopher Lowe with starfish on the shore of Stanford’s Hopkins Marine Station, in Monterey, California.
Photo Credit: LiPo Ching / Stanford University

A new study that combines genetic and molecular techniques helps solve the riddle of starfish body plans, and how starfish start life with bilateral body symmetry – just like humans – but grow up to be adults with fivefold “pentaradial” symmetry.

If you put a hat on a starfish, where would you put it? On the center of the starfish? Or on the point of an arm and, if so, which one? The question is silly, but it gets at serious questions in the fields of zoology and developmental biology that have perplexed veteran scientists and schoolchildren in introductory biology classes alike: Where is the head on a starfish? And how does their body layout relate to ours?

Now, a new Stanford study that used genetic and molecular tools to map out the body regions of starfish – by creating a 3D atlas of their gene expression – helps answer this longstanding mystery. The “head” of a starfish, the researchers found, is not in any one place. Instead, the headlike regions are distributed with some in the center of the sea star as well as in the center of each limb of its body.

Researchers observe wolves hunting and killing sea otters and harbor seals on Alaska’s Katmai coast

Wolf with a sea otter on Alaska's Katmai coast.
Photo Credit: Kelsey Griffin

Firsthand observations of a wolf hunting and killing a harbor seal and a group of wolves hunting and consuming a sea otter on Alaska’s Katmai coast have led scientists to reconsider assumptions about wolf hunting behavior.

Wolves have previously been observed consuming sea otter carcasses, but how they obtain these and the frequency of scavenging versus hunting marine prey is largely unknown. Scientists at Oregon State University, the National Park Service and Alaska Department of Fish and Game are beginning to change that with a paper just published in Ecology.

In the paper, they describe several incidents they observed involving wolves and marine mammals in Katmai National Park that they believe haven’t been previously documented:

Humans have substantially altered the relationship between wolves and deer

A breeding female wolf traveling on a logging road carrying a deer fawn back to her pups in June 2023.
 Photo Credit: Voyageurs Wolf Project

New research from the University of Minnesota’s Voyageurs Wolf Project found that human activities in northern Minnesota — logging, road and trail creation, and infrastructure development — have profoundly impacted where wolves hunt and kill deer fawns. By altering forest ecosystems, humans have created an environment that possibly favors predators. 

This research, recently published in Ecological Applications, is a collaboration between the University of Minnesota, Northern Michigan University, the University of Manitoba, Voyageurs National Park, and the Voyageurs Wolf Project. The Voyageurs Wolf Project is funded, in part, by the Minnesota Environment and Natural Resources Trust Fund as recommended by the Legislative-Citizen Commission on Minnesota Resources (LCCMR). 

“The premise is really quite simple: human activities change where deer are on the landscape, and wolves go where the deer are,” said co-lead author Thomas Gable, a postdoctoral researcher at the University of Minnesota and project lead for the Voyageurs Wolf Project. 

Fruit, nectar, bugs and blood: How bat teeth and jaws evolved for a diverse dinnertime

A side-view image of the skull of a greater spear-nosed bat, Phyllostomus hastatus, a noctilionoid species with an omnivorous diet.
Photo Credit: Sharlene Santana/University of Washington

They don’t know it, but Darwin’s finches changed the world. These closely related species — native to the Galapagos Islands — each sport a uniquely shaped beak that matches their preferred diet. Studying these birds helped Charles Darwin develop the theory of evolution by natural selection.

A group of bats has a similar — and more expansive — evolutionary story to tell. There are more than 200 species of noctilionoid bats, mostly in the American tropics. And despite being close relatives, their jaws evolved in wildly divergent shapes and sizes to exploit different food sources. A paper published in Nature Communications shows those adaptations include dramatic, but also consistent, modifications to tooth number, size, shape and position. For example, bats with short snouts lack certain teeth, presumably due to a lack of space. Species with longer jaws have room for more teeth — and, like humans, their total tooth complement is closer to what the ancestor of placental mammals had.

On the trail of a great mystery; how did the baboons get to ancient Egypt?

The first sequenced mitogenome of a mummified non-human primate connects an Egyptian ba-boon dated to ca. 800-540 BCE to modern baboon populations in Eritrea, Ethiopia and eastern Su-dan, providing evidence for Egyptian-Adulite trade centuries earlier than current archaeological evidence.
 Illustration Credit: © 2023 by Mike Costelloe
(CC BY-NC-ND 4.0.)

An interdisciplinary project led by primatologist Gisela Kopp is using genetic analysis to determine the geographic origin of mummified baboons found in ancient Egypt. The team finds evidence that the two legendary trading regions of Punt and Adulis may have been the same place separated by a thousand years of history.

In ancient Egypt, various deities were portrayed as animals. Thoth, the god of learning and wisdom was represented by a hamadryas baboon. Baboons, probably held in captivity in Egypt, were mummified as votive offerings after their deaths. Today, no wild baboons live in Egypt, and there is no evidence to suggest that these primates did so in the past. In an interdisciplinary project involving biologists, Egyptologists and anthropologists, Gisela Kopp, a biologist from Konstanz who conducts research on non-human primates, pursued the question of how and from where baboons came to Egypt. The results have been published in the current issue of the journal eLife.

Research reveals three new marsupial species – though all likely extinct

A Crest-Tail Mulgara.
Photo Credit: Bobby Tamayo, Simpson Desert, QLD

The exciting discovery of three new species of a small Australian marsupial has been tempered by the sad fact that each of the newly identified species of mulgara is likely already extinct.

The Curtin University-led study has identified three new species of mulgaras, which are small carnivorous marsupials related to the Tasmanian Devil and quoll and that are important to the arid and semi-arid regions they inhabit in South Australia, Western Australia, the Northern Territory and Queensland.

Led by Curtin PhD student Jake Newman-Martin, a collaboration with Dr Kenny Travouillon from the Western Australian Museum, Associate Professor Natalie Warburton from Murdoch University and Associate Professor Milo Barham and Dr Alison Blyth both from Curtin analyzed preserved specimens of mulgaras from museums across the country, including bones found in caves which had previously not been identifiable.

Mr. Newman-Martin said the research had identified six species of mulgaras, as opposed to the previously accepted two and it also concluded that a third previously named mulgara was indeed a valid species. However, four of the proposed species appeared to be already extinct.

Scientists uncover cause of mysterious deaths of elephants in Zimbabwe

Photo Credit: Charl Durand

During this unique study, scientists from the Victoria Falls Wildlife Trust, the Animal and Plant Health Agency UK, the University of Surrey and laboratories in South Africa investigated the mysterious deaths of 35 elephants mostly between August and September 2020, in a 40 x 25 km radius of North-Western Zimbabwe. This incident followed the death of approximately 350 elephants in neighboring northern Botswana from May to June 2020, which triggered much international concern. 

African savanna elephants are an endangered species with only 350,000 remaining in the wild and ongoing losses estimated at eight percent annually. This finding is very worrying since elephants are on the International Union for Conservation of Nature red list already. Investigating the deaths of these elephants is crucial to sustaining the future of this majestic species. 

New insights into the genetics of the common octopus: genome at the chromosome level decoded

Octopus vulgaris
Photo Credit: ©Antonio, Valerio Cirillo (BEOM SZN), 2023

Octopuses are fascinating animals – and serve as important model organisms in neuroscience, cognition research and developmental biology. To gain a deeper understanding of their biology and evolutionary history, validated data on the composition of their genome is needed, which has been lacking until now. Scientists from the University of Vienna together with an international research team have now been able to close this gap and, in a study, determined impressive figures: 2.8 billion base pairs - organized in 30 chromosomes. What sounds so simple is the result of complex, computer-assisted genome analyses and comparisons with the genomes of other cephalopod species. This groundbreaking research has just been published in the renowned journal G3: Genes / Genomes / Genetics.

Octopuses, together with squid and cuttlefish, belong to a group of coleoid cephalopods consisting of several hundreds of species that are characterized by highly diversified lifestyles, body structure and adaptations to their environment. The study of these animals looks back on a long tradition, especially since the neuronal plasticity of the octopus brain – meaning the brain's ability to change and adapt as you learn and experience new things – provides evidence for the existence of functionally analogous structures to the brains of mammals. This is making them a comparative model group for neurophysiological studies. Also, their ability to regenerate parts of their bodies as well as the rapid changes of their body patterns, which are important for camouflage and communication, make octopuses a popular research subject for studying how these innovative traits arose – and how they have changed – during evolution.

Marine mammals in zoos and aquariums now live 2-3 times longer than in the wild

Photo Credit: Los Muertos Crew

A new study provides compelling evidence that animal care and management practices at zoos and aquariums have significantly improved over time. The study, led by Species360 and University of Southern Denmark Research Scientist Dr. Morgane Tidière in collaboration with 41 co-authors from academic, governmental, and zoological institutions around the world, is the first to examine life expectancy and lifespan equality together as a proxy of population welfare in marine mammal species.

The study also found that marine mammal species live longer in zoological institutions than in the wild as a result of advances in animal care practices centered on animal welfare. The results have been published in Proceedings of the Royal Society B: Biological Sciences.

From SDU the following researchers contributed: Fernando Colchero, Johanna Staerk, Ditte H. Andersen, Kirstin Anderson Hansen and Dalia A. Conde.

The animals in the study
The four species in this study (harbor seal, sea lion, polar bear and bottlenose dolphin) were selected because they represent 63,4% of all marine mammals, registered in the global Species360 Zoological Information Management System (ZIMS).

Critical step made for managing brushtail possums

Researchers say mapping the genetic code of the brushtail possum will benefit those working to both conserve and control the animal.

In a five-year long study, just published in Nature Communications, an international group of researchers led by the University of Otago, has assembled the entire genetic code of the marsupial mammal.

The work also uncovered where and when their genes are expressed, and revealed surprising details about their population diversity, reproduction, and origins.

Study lead Associate Professor Tim Hore, of Otago’s Department of Anatomy, describes possums as “a fascinating animal that is loved in one country and a cause of concern in another”.

“They are hunted in Aotearoa New Zealand for their fur, and controlled for conservation, but treasured and protected in Australia. Having their full genetic code is important for both countries as efforts to manage their respective populations are being held back by the lack of this knowledge,” he says.