entomology

up-close-and-personal-with-the-stag-beetle-in-a-real-bug’s-life-s2

Up close and personal with the stag beetle in A Real Bug’s Life S2


It’s just one of the many fascinating insect species featured in the second season of this NatGeo docuseries.

A female giant stag beetle Credit: National Geographic/Darlyne A. Murawski

A plucky male American stag beetle thinks he’s found a mate on a rotting old tree stump—and then realizes there’s another male eager to make the same conquest. The two beetles face off in battle, until the first manages to get enough leverage to toss his romantic rival off the stump in a deft display of insect jujitsu. It’s the first time this mating behavior has been captured on film, and the stag beetle is just one of the many fascinating insects featured in the second season of A Real Bug’s Life, a National Geographic docuseries narrated by Awkwafina.

The genesis for the docuseries lies in a past rumored sequel to Pixar’s 1998 animated film A Bug’s Life, which celebrated its 25th anniversary two years ago. That inspired producer Bill Markham, among others, to pitch a documentary series on a real bug’s life to National Geographic. “It was the quickest commission ever,” Markham told Ars last year. “It was such a good idea, to film bugs in an entertaining family way with Pixar sensibilities.” And thanks to the advent of new technologies—photogrammetry, probe and microscope lenses, racing drones, ultra-high-speed camera—plus a handful of skilled “bug wranglers,” the team was able to capture the bug’s-eye view of the world beautifully.

As with the Pixar film, the bugs (and adjacent creatures) are the main characters here, from cockroaches, monarch butterflies, and praying mantises to bees, spiders, and even hermit crabs. The 10 episodes, across two seasons, tell their stories as they struggle to survive in their respective habitats, capturing entire ecosystems in the process: city streets, a farm, the rainforest, a Texas backyard, and the African savannah, for example. Highlights from S1 included the first footage of cockroach egg casings hatching; wrangling army ants on location in a Costa Rica rainforest; and the harrowing adventures of a tiny jumping spider navigating the mean streets of New York City.

Looking for love

A luna moth perched on a twig. National Geographic/Nathan Small

S2 takes viewers to Malaysia’s tropical beaches, the wetlands of Derbyshire in England, and the forests of Tennessee’s Smoky Mountains. Among the footage highlights: Malaysian tiger beetles, who can run so fast they temporarily are unable to see; a young female hermit crab’s hunt for a bigger shell; and tiny peacock spiders hatching Down Under. There is also a special behind-the-scenes look for those viewers keen to learn more about how the episodes were filmed, involving 130 different species across six continents. Per the official synopsis:

A Real Bug’s Life is back for a thrilling second season that’s bolder than ever. Now, thanks to new cutting-edge filming technology, we are able to follow the incredible stories of the tiny heroes living in this hidden world, from the fast-legged tiger beetle escaping the heat of Borneo’s beaches to the magical metamorphosis of a damselfly on a British pond to the Smoky Mountain luna moth whose quest is to grow wings, find love and pass on his genes all in one short night. Join our witty guide, Awkwafina, on new bug journeys full of more mind-blowing behaviors and larger-than-life characters.

Entomologist Michael Carr, an environmental compliance officer for Santa Fe County in New Mexico, served as a field consultant for the “Love in the Forest” episode, which focuses on the hunt for mates by a luna moth, a firefly, and an American stag beetle. The latter species is Carr’s specialty, ever since he worked at the Smithsonian’s Museum of Natural History and realized the beetles flourished near where he grew up in Virginia. Since stag beetles are something of a niche species, NatGeo naturally tapped Carr as its field expert to help them find and film the insects in the Smoky Mountains. To do so, Carr set up a mercury vapor lamp on a tripod—”old style warehouse lights that take a little time to charge up,” which just happen to emit frequencies of light that attract different insect species.

Behind the scenes

Beetle expert Michael Carr and shooting researcher Katherine Hannaford film a stag beetle at night. National Geographic/Tom Oldridge

Stag beetles are saprocylic insects, according to Carr, so they seek out decaying wood and fungal communities. Males can fly as high as 30 feet to reach tree canopies, while the females can dig down to between 1 and 3 meters to lay their eggs in wood. Much of the stag beetle’s lifecycle is spent underground as a white grub molting into larger and larger forms before hatching in two to three years during the summer. Once their exoskeletons harden, they fly off to find mates and reproduce as quickly as possible. And if another male happens to get in their way, they’re quite prepared to do battle to win at love.

Stag beetles might be his specialty, but Carr found the fireflies also featured in that episode to be a particular highlight. “I grew up in rural Virginia,” Carr told Ars. “There was always fireflies, but I’d never seen anything like that until I was there on site. I did not realize, even though I’d grown up in the woods surrounded by fireflies, that, ‘Oh, the ones that are twinkling at the top, that’s one species. The ones in the middle that are doing a soft glow, that’s a different species.'”

And Carr was as surprised and fascinated as any newbie to learn about the “femme fatale” firefly: a species in which the female mimics the blinking patterns of other species of firefly, luring unsuspecting males to their deaths. The footage captured by the NatGeo crew includes a hair-raising segment where this femme fatale opts not to wait for her prey to come to her. A tasty male firefly has been caught in a spider’s web, and our daring, hungry lady flies right into the web to steal the prey:

A femme fatale firefly steals prey from a rival spider’s web.

Many people have a natural aversion to insects; Carr hopes that inventive docuseries like A Real Bug’s Life can help counter those negative perceptions by featuring some lesser-loved insects in anthropomorphized narratives—like the cockroaches and fire ants featured in S1. “[The series] did an amazing job of showing how something at that scale lives its life, and how that’s almost got a parallel to how we can live our life,” he said. “When you can get your mindset down to such a small scale and not just see them as moving dots on the ground and you see their eyes and you see how they move and how they behave and how they interact with each other, you get a little bit more appreciation for ants as a living organism.”

“By showcasing some of the bigger interesting insects like the femme fatale firefly or the big chivalrous stag beetle fighting over each other, or the dung beetle getting stomped by an elephant—those are some pretty amazing just examples of the biodiversity and breadth of insect life,” said Carr. “People don’t need to love insects. If they can, just, have some new modicum of respect, that’s good enough to change perspectives.”

The second season of A Real Bug’s Life premieres on January 15, 2025, on Disney+.

Photo of Jennifer Ouellette

Jennifer is a senior writer at Ars Technica with a particular focus on where science meets culture, covering everything from physics and related interdisciplinary topics to her favorite films and TV series. Jennifer lives in Baltimore with her spouse, physicist Sean M. Carroll, and their two cats, Ariel and Caliban.

Up close and personal with the stag beetle in A Real Bug’s Life S2 Read More »

ants-vs.-humans:-solving-the-piano-mover-puzzle

Ants vs. humans: Solving the piano-mover puzzle

Who is better at maneuvering a large load through a maze, ants or humans?

The piano-mover puzzle involves trying to transport an oddly shaped load across a constricted environment with various obstructions. It’s one of several variations on classic computational motion-planning problems, a key element in numerous robotics applications. But what would happen if you pitted human beings against ants in a competition to solve the piano-mover puzzle?

According to a paper published in the Proceedings of the National Academy of Sciences, humans have superior cognitive abilities and, hence, would be expected to outperform the ants. However, depriving people of verbal or nonverbal communication can level the playing field, with ants performing better in some trials. And while ants improved their cognitive performance when acting collectively as a group, the same did not hold true for humans.

Co-author Ofer Feinerman of the Weizmann Institute of Science and colleagues saw an opportunity to use the piano-mover puzzle to shed light on group decision-making, as well as the question of whether it is better to cooperate as a group or maintain individuality. “It allows us to compare problem-solving skills and performances across group sizes and down to a single individual and also enables a comparison of collective problem-solving across species,” the authors wrote.

They decided to compare the performances of ants and humans because both species are social and can cooperate while transporting loads larger than themselves. In essence, “people stand out for individual cognitive abilities while ants excel in cooperation,” the authors wrote.

Feinerman et al. used crazy ants (Paratrechina longicornis) for their experiments, along with the human volunteers. They designed a physical version of the piano-movers puzzle involving a large t-shaped load that had to be maneuvered across a rectangular area divided into three chambers, connected via narrow slits. The load started in the first chamber on the left, and the ant and human subjects had to figure out how to transport it through the second chamber and into the third.

Ants vs. humans: Solving the piano-mover puzzle Read More »

call-the-ant-doctor:-amputation-gives-injured-ants-a-leg-up-on-infections

Call the ant doctor: Amputation gives injured ants a leg up on infections

video still image showing woundcare and amputation in C. maculatus

Enlarge / Scientists have observed wound care and selective amputation in Florida carpenter ants.

Florida carpenter ants (Camponotus floridanus) selectively treat the wounded limbs of their fellow ants, according to a new paper published in the journal Current Biology. Depending on the location of the injury, the ants either lick the wounds to clean them or chew off the affected limb to keep infection from spreading. The treatment is surprisingly effective, with survival rates of around 90–95 percent for amputee ants.

“When we’re talking about amputation behavior, this is literally the only case in which a sophisticated and systematic amputation of an individual by another member of its species occurs in the animal kingdom,” said co-author Erik Frank, a behavioral ecologist at the University of Würzburg in Germany. “The fact that the ants are able to diagnose a wound, see if it’s infected or sterile, and treat it accordingly over long periods of time by other individuals—the only medical system that can rival that would be the human one.”

Frank has been studying various species of ants for many years. Late last year, he co-authored a paper detailing how Matabele ants (Megaponera analis) south of the Sahara can tell if an injured comrade’s wound is infected or not, thanks to chemical changes in the hydrocarbon profile of the ant cuticle when a wound gets infected. These ants only eat termites, but termites have powerful jaws and use them to defend against predators, so there is a high risk of injury to hunting ants.

If an infected wound is identified, the ants then treat said wound with antibiotics produced by a special gland on the side of the thorax (the metapleural gland). Those secretions are made of some 112 components, half of which have antimicrobial properties. Frank et al.’s experiments showed that applying these secretions reduced the mortality rate of injured ants by 90 percent, and future research could lead to the discovery of new antibiotics suitable for treating humans. (This work was featured in an episode of a recent Netflix nature documentary, Life on Our Planet.)

Amputation in Camponotus maculatus. Credit: Danny Buffat.

Those findings caused Frank to ponder if the Matabele ant is unique in its ability to detect and treat infected wounds, so he turned his attention to the Florida carpenter ant. These reddish-brown ants nest in rotting wood and can be fiercely territorial, defending their homes from rival ant colonies. That combat comes with a high risk of injury. Florida carpenter ants lack a metapleural gland, however, so Frank et al. wondered how this species treats injured comrades. They conducted a series of experiments to find out.

Frank et al. drew their subjects from colonies of lab-raised ants (produced by queens collected during 2017 fieldwork in Florida), and ants targeted for injury were color-tagged with acrylic paint two days before each experiment. Selective injuries to tiny (ankle-like) tibias and femurs (thighs) were made with sterile Dowel-scissors, and cultivated strains of P. aeruginosa were used to infect some of those wounds, while others were left uninfected as a control. The team captured the subsequent treatment behavior of the other ants on video and subsequently analyzed that footage. They also took CT scans of the ants’ legs to learn more about the anatomical structure.

Call the ant doctor: Amputation gives injured ants a leg up on infections Read More »

the-wasps-that-tamed-viruses

The wasps that tamed viruses

Parasitoid wasp

Enlarge / Xorides praecatorius is a parasitoid wasp.

If you puncture the ovary of a wasp called Microplitis demolitor, viruses squirt out in vast quantities, shimmering like iridescent blue toothpaste. “It’s very beautiful, and just amazing that there’s so much virus made in there,” says Gaelen Burke, an entomologist at the University of Georgia.

M. demolitor  is a parasite that lays its eggs in caterpillars, and the particles in its ovaries are “domesticated” viruses that have been tuned to persist harmlessly in wasps and serve their purposes. The virus particles are injected into the caterpillar through the wasp’s stinger, along with the wasp’s own eggs. The viruses then dump their contents into the caterpillar’s cells, delivering genes that are unlike those in a normal virus. Those genes suppress the caterpillar’s immune system and control its development, turning it into a harmless nursery for the wasp’s young.

The insect world is full of species of parasitic wasps that spend their infancy eating other insects alive. And for reasons that scientists don’t fully understand, they have repeatedly adopted and tamed wild, disease-causing viruses and turned them into biological weapons. Half a dozen examples already are described, and new research hints at many more.

By studying viruses at different stages of domestication, researchers today are untangling how the process unfolds.

Partners in diversification

The quintessential example of a wasp-domesticated virus involves a group called the bracoviruses, which are thought to be descended from a virus that infected a wasp, or its caterpillar host, about 100 million years ago. That ancient virus spliced its DNA into the genome of the wasp. From then on, it was part of the wasp, passed on to each new generation.

Over time, the wasps diversified into new species, and their viruses diversified with them. Bracoviruses are now found in some 50,000 wasp species, including M. demolitor. Other domesticated viruses are descended from different wild viruses that entered wasp genomes at various times.

Researchers debate whether domesticated viruses should be called viruses at all. “Some people say that it’s definitely still a virus; others say it’s integrated, and so it’s a part of the wasp,” says Marcel Dicke, an ecologist at Wageningen University in the Netherlands who described how domesticated viruses indirectly affect plants and other organisms in a 2020 paper in the Annual Review of Entomology.

As the wasp-virus composite evolves, the virus genome becomes scattered through the wasp’s DNA. Some genes decay, but a core set is preserved—those essential for making the original virus’s infectious particles. “The parts are all in these different locations in the wasp genome. But they still can talk to each other. And they still make products that cooperate with each other to make virus particles,” says Michael Strand, an entomologist at the University of Georgia. But instead of containing a complete viral genome, as a wild virus would, domesticated virus particles serve as delivery vehicles for the wasp’s weapons.

Here are the steps in the life of a parasitic wasp that harbors a bracovirus.

Enlarge / Here are the steps in the life of a parasitic wasp that harbors a bracovirus.

Those weapons vary widely. Some are proteins, while others are genes on short segments of DNA. Most bear little resemblance to anything found in wasps or viruses, so it’s unclear where they originated. And they are constantly changing, locked in evolutionary arms races with the defenses of the caterpillars or other hosts.

In many cases, researchers have yet to discover even what the genes and proteins do inside the wasps’ hosts or prove that they function as weapons. But they have untangled some details.

For example, M. demolitor  wasps use bracoviruses to deliver a gene called glc1.8  into the immune cells of moth caterpillars. The glc1.8  gene causes the infected immune cells to produce mucus that prevents them from sticking to the wasp’s eggs. Other genes in M. demolitor’s bracoviruses force immune cells to kill themselves, while still others prevent caterpillars from smothering parasites in sheaths of melanin.

The wasps that tamed viruses Read More »

why-are-there-so-many-species-of-beetles?

Why are there so many species of beetles?

The beetles outnumber us —

Diet played a key role in the evolution of the vast beetle family tree.

A box of beetles

Caroline Chaboo’s eyes light up when she talks about tortoise beetles. Like gems, they exist in myriad bright colors: shiny blue, red, orange, leaf green and transparent flecked with gold. They’re members of a group of 40,000 species of leaf beetles, the Chrysomelidae, one of the most species-rich branches of the vast beetle order, Coleoptera. “You have your weevils, longhorns, and leaf beetles,” she says. “That’s really the trio that dominates beetle diversity.”

An entomologist at the University of Nebraska, Lincoln, Chaboo has long wondered why the kingdom of life is so skewed toward beetles: The tough-bodied creatures make up about a quarter of all animal species. Many biologists have wondered the same thing, for a long time. “Darwin was a beetle collector,” Chaboo notes.

Despite their kaleidoscopic variety, most beetles share the same three-part body plan. The insects’ ability to fold their flight wings, origami-like, under protective forewings called elytra allows beetles to squeeze into rocky crevices and burrow inside trees. Beetles’ knack for thriving in a large range of microhabitats could also help explain their abundance of species, scientists say.

Enlarge / Despite their kaleidoscopic variety, most beetles share the same three-part body plan. The insects’ ability to fold their flight wings, origami-like, under protective forewings called elytra allows beetles to squeeze into rocky crevices and burrow inside trees. Beetles’ knack for thriving in a large range of microhabitats could also help explain their abundance of species, scientists say.

Of the roughly 1 million named insect species on Earth, about 400,000 are beetles. And that’s just the beetles described so far. Scientists typically describe thousands of new species each year. So—why so many beetle species? “We don’t know the precise answer,” says Chaboo. But clues are emerging.

One hypothesis is that there are lots of them because they’ve been around so long. “Beetles are 350 million years old,” says evolutionary biologist and entomologist Duane McKenna of the University of Memphis in Tennessee. That’s a great deal of time in which existing species can speciate, or split into new, distinct genetic lineages. By way of comparison, modern humans have existed for only about 300,000 years.

Yet just because a group of animals is old doesn’t necessarily mean it will have more species. Some very old groups have very few species. Coelacanth fish, for example, have been swimming in the ocean for approximately 360 million years, reaching a maximum of around 90 species and then declining to the two species known to be living today. Similarly, the lizard-like reptile the tuatara is the only living member of a once globally diverse ancient order of reptiles that originated about 250 million years ago.

Another possible explanation for why beetles are so rich in species is that, in addition to being old, they have unusual staying power. “They have survived at least two mass extinctions,” says Cristian Beza-Beza, a University of Minnesota postdoctoral fellow. Indeed, a 2015 study using fossil beetles to explore extinctions as far back as the Permian 284 million years ago concluded that lack of extinction may be at least as important as diversification for explaining beetle species abundance. In past eras, at least, beetles have demonstrated a striking ability to shift their ranges in response to climate change, and this may explain their extinction resilience, the authors hypothesize.

Why are there so many species of beetles? Read More »

the-entire-state-of-illinois-is-going-to-be-crawling-with-cicadas

The entire state of Illinois is going to be crawling with cicadas

BUZZ BUZZ BUZZ BUZZ BUZZ —

And the land shall feast on their dead.

Adult periodical cicada

Ed Reschke via Getty

Brace yourselves, Illinoisans: A truly shocking number of cicadas are about to live, make sweet love, and die in a tree near you. Two broods of periodical cicadas—Brood XIX on a 13-year cycle and Brood XIII on a 17-year cycle—are slated to emerge together in central Illinois this summer for the first time in over two centuries. To most humans, they’re an ephemeral spectacle and an ear-splitting nuisance, and then they’re gone. To many other Midwestern animals, plants, and microbes, they’re a rare feast, bringing new life to forests long past their death.

From Nebraska to New York, 15 broods of periodical cicadas grow underground, quietly sipping watery sap from tree roots. After 13 or 17 years (depending on the brood), countless inch-long adults dig themselves out in sync, crawling out of the ground en masse for a monthlong summer orgy. After mating, they lay eggs in forest trees and die, leaving their tree-born babies to fall to the forest floor and begin the cycle anew. Cicadas don’t fly far from their birthplace, so each brood occupies a distinct patch of the US. “They form a mosaic on the landscape,” says Chris Simon, senior research scientist in ecology and evolutionary biology at the University of Connecticut.

Most years, at least one of these 15 broods emerges (annual cicadas, not to be confused with their smaller periodical cousins, pop up separately every summer). Sometimes two broods emerge at the same time. It’s also not unheard of for multiple broods to coexist in the same place. “What’s unusual is that these two broods are adjacent,” says John Lill, insect ecologist at George Washington University. “Illinois is going to be ground zero. From the very top to the very bottom of the state, it’s going to be covered in cicadas.” The last time that these broods swarmed aboveground together, Thomas Jefferson was president and the city of Chicago had yet to exist.

Entomologists around the world already have their flights booked for May. “We’re like cicada groupies,” Lill says. He promises that this once-in-a-generation spectacle will be even better than April’s total solar eclipse. During 2004’s Brood X emergence, Lill remembers walking outside at midnight. “For two seconds, I was like, ‘Wow, I didn’t know it was raining,’ because I saw water flowing down the street. As my eyes focused, I realized it was literally just thousands of cicadas crawling across the street.”

Some cicada devotees, like author and entomologist Greg Kritsky, have already witnessed Brood XIII emerge a couple of times. But for most of their predators, a brood emergence happens once in a lifetime, and it’s always an extremely pleasant surprise. “It’s a food bonanza,” Kritsky says, “like if you walked outside and found the whole world swarming with flying Hershey’s Kisses.”

Cicadas are shockingly chill, protein-packed, and taste like high-end shrimp—easy, delicious prey. “Periodical cicadas are sitting ducks,” says Lill. They don’t bite, sting, or poison anyone, and they’re totally unbothered by being handled. Dogs, raccoons, birds, and other generalist predators will gorge themselves on this flying feast until they’re stuffed, and it barely makes a dent in the cicada population. It’s their secret weapon, Lill says: In the absence of other defense mechanisms, “they just overwhelm predators by their sheer abundance.”

Much like an unexpected free dinner will distract you from the leftovers sitting in your fridge, this summer’s cicada emergence will turn predators away from their usual prey. During the 2021 Brood X emergence, Zoe Getman-Pickering, a scientist in Lill’s research group, found that as birds swooped in on cicadas, caterpillar populations exploded. Spared from birds, caterpillars chomped on twice as many oak leaves as normal—and the chain of effects went on and on. Scientists can’t possibly study them all. “The ecosystem gets a swift kick, with this unexpected perturbation that changes a lot of things at once,” says Louie Yang, an ecologist and professor of entomology at UC Davis.

From birth to death, these insects shape the forest around them. As temperatures rise in late April, pale, red-eyed cicada nymphs begin clawing pinky-sized holes in the ground, preparing for their grand May entrance. All of these tunnels make it easier for rainwater to move through the soil, where it can then be used by plants and other dirt-inhabiting microbes. Once fully grown and aboveground, adult cicadas shed their exoskeletons, unfurl their wings, and fly off to spend their remaining four to six weeks on Earth singing (if they’re male), listening for the sexiest songs (if they’re female), and mating.

Mother cicadas use the metal-enhanced saws built into their abdomens—wood-drilling shafts layered with elements like aluminum, copper, and iron—to slice pockets into tree branches, where they’ll lay roughly 500 eggs each. Sometimes, all of these cuts cause twigs to wither or snap, killing leaves. While this could permanently damage a very young sapling, mature trees simply shed the slashed branches and carry on. “It’s like natural pruning,” Kritsky says, which keeps hearty trees strong, prevents disease, and promotes flower growth.

Once mating season winds down, so does the cicada’s life. “In late summer, everybody forgets about cicadas,” Lill says. “They all die. They all rot in the ground. And then they’re gone.” By late June, there will be millions of pounds of cicadas piling up at the base of trees, decomposing. The smell, Kritsky says, “is a sentient memory you will never forget—like rancid Limburger cheese.”

But these stinky carcasses send a massive pulse of food to scavengers in the soil. “The cicadas serve as reservoirs of nutrients,” Yang says. “When they come out, they release all this stored energy into the ecosystem,” giving their bodies back to the plants that raised them. In the short term, dead cicadas have a fertilizing effect, feeding microbes in the soil and helping plants grow larger. And as their remnants make their way into woodland ponds and streams, cicada nutrients are carried downstream, where they may strengthen aquatic ecosystems far beyond their home tree.

They may smell like bad hamburgers, but Yang says that if you’re lucky enough to host a tree full of cicadas this year, it’s best to just leave their bodies alone to decompose naturally. “They’ll be gone soon enough,” he says. If the pileup is especially obtrusive, simply sweep them out of the way and let nature do the rest.

The thought of billions of screeching insects in your backyard might make your skin crawl, but you don’t need to be a passive observer when they arrive. Researchers are clamoring for citizen scientists to send in photos of their local cicadas to help map the upcoming emergence. The Cicada Safari app, developed by Kritsky, received and verified 561,000 cicada pics during the 2021 Brood X emergence—he hopes to get even more this time around.

“This is an amazing natural phenomenon to wonder about,” Lill says, “not something to be afraid of.”

This story originally appeared on wired.com.

The entire state of Illinois is going to be crawling with cicadas Read More »