Pick an animal.

Choose wisely because in this fantasy you’ll transform into the creature and duel against one of your own. If you care about survival, go for the muscular, multispiked stag roaring at a rival. Never, ever pick the wingless male fig wasp. Way too dangerous.

This advice sounds exactly wrong. But that’s because many stereotypes of animal conflict get the real biology backward. All-out fighting to the death is the rule only for certain specialized creatures. Whether a species is bigger than a breadbox has little to do with lethal ferocity.

Many creatures that routinely kill their own kind would be terrifying, if they were larger than a jelly bean. Certain male fig wasps unable to leave the fruit they hatch in have become textbook examples, says Mark Briffa, who studies animal combat. Stranded for life in one fig, these males grow “big mouthparts like a pair of scissors,” he says, and “decapitate as many other males as they possibly can.” The last he-wasp crawling has no competition to mate with all the females in his own private fruit palace.
In contrast, big mammals that inspire sports-team mascots mostly use antlers, horns and other outsize male weaponry for posing, feinting and strength testing. Duels to the death are rare.

“In the vast majority of cases, what we think of as fights are solved without any injuries at all,” says Briffa, of Plymouth University in England.

Evolution has produced a full rainbow of conflict styles, from the routine killers to animals that never touch an adversary. Working out how various species in that spectrum assess when it’s worth their while to go head-to-head has become a challenging research puzzle.“In the vast majority of cases, what we think of as fights are solved without any injuries at all,” says Briffa, of Plymouth University in England.

To untangle the rules of engagement, researchers are turning to animals that live large in small bodies but don’t have sports teams named after them. At least not yet.
Deadliest matches
It’s hard to imagine nematodes fighting at all. There’s little, if any, weaponry visible on the see-through, micronoodle body of the species called Steinernema longicaudum. Yet in Christine Griffin’s lab at Maynooth University in Ireland, a graduate student offered a rare hermaphrodite to a male as a possible mate. Instead of mating, the male went in for the kill.
“We thought, well, poor hermaphrodite, she’s not used to mating, so maybe it’s just some kind of accident,” says Griffin, whose lab specializes in nematodes as pest control for insects. When the grad student, Kathryn O’Callaghan, offered females of another species, males killed some of those females too. When given a chance, males also readily killed each other. That’s how nematodes, in 2014, joined the list of kill-your-own-kind animals, Griffin says.
Killing another nematode is an accomplishment for a skinny thread of an animal with just two thin, protruding prongs. The male S. longicaudum slays by repurposing his mating moves.

When he encounters a female of his own species, the male coils his tail around her and positions the prongs, known as spicules, to hold open the entrance to her reproductive tract. To kill, a male just coils his tail around another male, or a female of a different species, and squeezes extra hard. Pressure ruptures internal organs; sometimes spicules even punch a hole during the fatal embrace. The grip lasts from a few seconds to several minutes. Of those worms paralyzed by the attack, most are dead the next day.

Other nematodes live in labs around the world without murdering each other. So why does S. longicaudum, for one, lean toward extreme violence? Its lifestyle of colonizing the innards of an insect inclines it to kill, Griffin suggests. An insect larva is a prize one male worm can monopolize, not to mention the only place he can have sex.

These nematodes lurk in soil without reproducing or even feeding until they find a promising target, such as the pale fat larva of a black vine weevil. Nematodes wriggle in through any opening: the larva’s mouth, breathing pores, anus. If a male kills all rivals inside his new home, he becomes the nematode Adam for generations of offspring perhaps totaling in the hundreds of thousands, Griffin says.
Territorial female slayers
A defendable bonanza like a weevil larva, or a fig, has become a theme in the evolution of lethal fighting. Biologists have studied violence in certain male fig wasps for decades, but more recent research has revealed that some females kill each other too.

When a female Pegoscapus wasp, a bit longer than a poppy seed, chooses one particular pea-sized sac of flowers, a fig-to-be, she’s deciding her destiny. That sac is most likely her only chance at laying eggs, and will probably be the fruit she will die in, says evolutionary ecologist Charlotte Jandér of Harvard University.

Shortleaf fig trees (Ficus citrifolia) have “a delicate flowery smell,” Jandér says, but the blooms are hidden inside the little green-skinned sacs. To reach these inner riches and lay one egg per flower in as many flowers as she can, the wasp must push through a tight tunnel. The squeeze can take roughly half an hour and rip her wings and antennae. Reaching the inner cavity carpeted in whitish flowers, “there is plenty of space for one wasp to move around,” Jandér says. But more than one gets cramped, and conflicts get desperate.

In a Panamanian wasp species that Jandér has watched, females “can lock on to each other’s jaws for hours and push back and forth,” she says. In a Brazilian species, 31 females were found decapitated among 84 wasps, reported Jandér, Rodrigo A.S. Pereira of the University of São Paulo and colleagues in 2015. That was the first documented female-to-female killing in fig wasps.

Walk away
From bellowing red deer stags to confrontational male stalk-eyed flies, many animal species have ways to back off rather than fight to the death. Searching for dynamics of less-than-deadly discord, Briffa studies sea anemones. And yes, anemones fight.
Beadlet sea anemones (

Actinia equina

) release sperm and eggs into open seawater, so the animals don’t need to argue over mates. For a prime bit of tide pool rock, however, tensions rise.

Below a beadlet’s pinkish, swaying food-catcher tentacles are what often look like “little blue beads,” Briffa says. These are fighting tentacles, or acrorhagi. When combat looms, the anemone inflates them. “Imagine someone pulling out their bottom lip to make a funny face,” he says.

It’s no joke for an impertinent neighbor. Anemones, distant relatives of stinging jellies, carry harpoon-shooting, toxin-injecting capsules in the acrorhagi. Combatants rake stinger acrorhagi down each other’s soft flesh. “It almost looks like they’re punching each other,” Briffa says. “When one of the anemones decides it’s had enough and wants to quit the contest, it actually actively walks away.”

“Walk” is used loosely here, says Sarah Lane, a postdoc in Briffa’s lab, as she alternately arches her hand and flattens it in a measured trip across the Skype screen. “Like a cartoon caterpillar?” she says, trying to describe the gait. “A concertina?”
When placed side by side in the lab for fighting tests, anemones concertina away or otherwise resolve the tension without any acrorhagi swipes about a third of the time. De-escalating makes sense considering that a full exchange “looks quite vicious,” Lane says. Strikes leave behind bluish fragments of acrorhagi full of stinging capsules, which kill tissue on the recipient. The attacker isn’t unscathed either; close-ups show open wounds where acrorhagi tissue was pulled out. An anemone “literally can’t hurt an opponent without ripping parts of itself off,” she says.

Injuries to an attacker from swiping, biting or other acts of aggression get overlooked in theorizing over how animals weigh the costs and benefits of dueling, Lane and Briffa argued in the April 2017 Animal Behaviour. The sea anemones may be an extreme example of self-harm from a strike, but they’re not the only one.

Humans can hurt themselves when they attack, and decision making around fighting has had some unintended consequences, Lane points out. In a bare-handed punch at somebody’s head, little bones in the hand crack — called boxer’s fractures — before the skull does. With the introduction of gloves around 1897, boxer’s fractures basically disappeared from match records, Lane says. Before gloves, however, records show no reported deaths in professional matches. Once gloves lessened the costs of delivering high-impact punches, deaths began appearing in the records.

Worth the fight?
Sea anemones don’t have a brain or centralized nervous system, yet costs and benefits of fighting somehow still matter. The animals clearly pick their fights, escalating some blobby sting matches and creeping away from others.

Just how anemones choose, or how any animal chooses when to fight and when to back down, turns out to be a rich vein for research. Theorists have proposed versions of two basic approaches. One, called mutual assessment, “is sussing out when you’re weaker and giving up as soon as you know — that’s the smart way,” Briffa says. Yet the evidence Briffa has so far, he says with perhaps a touch of wistfulness, suggests anemones use “the dumb way of giving up.”

Animals resort to this “dumb” option, called self-assessment, when they can’t compare their opponent’s odds of winning with their own. Maybe they fight in shadowy, murky places. Maybe they don’t have the neural capacity for that kind of comparison. For whatever reason, they’re stuck with “keep going until you can’t keep going anymore,” he says. Never mind if the fight is hopeless from the beginning.

The odds of fighting “smart” look better for the animals that Patrick Green of Duke University studies. Those creatures have a brainlike ganglion and come close to fighting with superpowers. He’s working with, of course, mantis shrimp.

The high-powered smashers among these small crustaceans flick out a club that can accelerate as fast as a bullet shooting out of a .22 caliber pistol. When the clubs wham a tasty snail, the bounce back creates a low-pressure zone that vaporizes water. “I always feel weird saying this because it seems just goofy, but that does release heat equivalent to the surface of the sun,” Green says. But only for a fraction of a microsecond.

When smasher mantis shrimp — male or female — fight each other, they don’t supernova rivals into oblivion. The reality, arguably stranger, is that they superpunch each other. But the blows land on an area that can withstand the force: the telson, a bumpy shield covering the rump (SN: 7/11/15, p. 13).

In Caribbean rock mantis shrimp (Neogonodactylus bredini), the battle is often over after just one to five blows too fast for the human eye to see. With combatants of equal size, the winner is not the animal that lands the most forceful blow, but the one that gets in the most punches. Then, with no visible gore, one dueler just gives up.
Now Green and Sheila Patek, also of Duke, propose that telson sparring, as they call it,

permits genuine mutual assessment, the smart way of losing a fight

. It’s difficult to figure out what lurks in the neural circuits of an arthropod, but the researchers presented multiple lines of evidence in the Jan. 31

Proceedings of the Royal Society B.

One strong clue came from matches Green staged between mantis shrimp of different sizes. He didn’t see a trend of smaller ones pointlessly pounding telsons as the lightweights fought bigger animals. Those bigger animals were going to win anyway, and it seemed as if the smaller ones got it, suggesting something more than self-assessment is going on, Green and Patek propose.

Researchers think they have seen mutual assessment in other animals too, among wrestling male New Zealand giraffe weevils (SN: 10/4/14, p. 4) and male jumping spiders that flip up banded legs in “Goal!” position to intimidate rivals. Analyzing assessment gets tricky. Game theorists have weighed in, but there’s debate over what kind of biological evidence truly distinguishes one form of assessment from another. And research in new directions is bringing more biological realism to the discussion of conflicts. Human scientists, dazzled by the sights and sounds that our own sensory world emphasizes, may be underestimating chemical cues. Among crawfish, “part of their fight is squirting urine in one another’s faces,” Briffa says.

Paradoxically peaceful
Many of the scariest-looking weapons end up causing little bodily harm. Some are specialized for combat that’s more strategic than gory. Other weapons look so scary they hardly ever get used.

Among the tools for odd but not life-threatening combat are the horns of the male Asian rhinoceros beetles studied by Erin McCullough, now at the University of Western Australia in Perth. Male Trypoxylus dichotomus compete furiously with each other and grow forked horns on their heads that stretch nearly two-thirds the beetle’s body length. The horns are surprisingly lightweight, but look cumbersome. “Like a Styrofoam leg sticking out of your forehead,” she says.
She watched the beetles in action on a muggy summer night lurking around ash trees at a university in Taiwan. Hardly blending in with the students, she decked out in leather gloves and a head lamp, making sure her shirts had the collars pulled way up. “You shouldn’t wear mosquito repellant when you’re working with insects,” she says.

The scene was “really messy and chaotic,” she recalls. Beetles flying out of the dark fought to dominate cracks in ash tree bark that oozed sap and attracted females. A dominant beetle would grip the bark and use his horn to flick incoming challengers off the branch left and right — until he was usurped. Getting thrown off the limb doesn’t kill losers; often they buzz right back for another try.

Yet evolutionarily speaking, a male prevented from mating might as well be dead, so the tactic was consequential. Males with longer horns are better at flicking off other males, but longer horns are more likely to snap, McCullough concluded. A broken horn doesn’t grow back, so the extravagant tool needs to be a pry bar of the right length, lightness and strength. Pristine horns on male beetles just starting their fighting careers have about four times the strength the horns need to resist cracking, about the safety factor that engineers build into bridges but less than the standard for elevator cables, she says.

Horns or antlers on male mammals often can kill, yet fatal fights may be rare. One of his favorite studies from decades-old literature, says Douglas Emlen of the University of Montana in Missoula, looked at about 1,308 sparring matches between male caribou in Alaska. With all this glaring, snorting and rushing, only six matches escalated into violent, bloody fights.

The caribou fit one of the paradoxical phases of the evolution of animal weaponry that Emlen studies. Usually evolution doesn’t favor extremes in teeth, horns or other such fighting body parts. Certain forms of sexual rivalry, however, can escape such stabilizing forces and expand extravagantly in a body-part arms race. There are common patterns to such arms races, he says, including some cheating.

Among the conditions that favor an arms race are rivalries playing out in one-on-one duels, he says. Imagine a magnificently endowed dung beetle in a tunnel, a female in the depths behind him, as he fends off rivals one by one for her attention. Growing bigger and bigger horns for an arms race becomes biologically expensive. Eventually, only an animal with the best nutrition, genes and luck can spare the resources to grow a truly commanding horn. At that point, horn size honestly signals a male that can overpower just about all rivals. Only if he confronts another supermale will he need to fight all out. The rest of the time, the signal value of his prodigious weaponry keeps the peace with barely a bump or a bruise.

Yet this is “a very unstable situation,” Emlen says. “It creates incentives for males to cheat.” Or maybe the word is “innovate.” He found that big-horned male dung beetles defending their tunnels could be outmaneuvered by small rivals who dug bypass tunnels around the guard zone and mated with the supposedly defended female. Beetle horns may not be the best analogy for human nuclear arsenals, but, Emlen notes, the innovations of cyberattacks have certainly bypassed hugely expensive national defense systems.

At the far extreme of animal rivalries are some species that blur the meaning of fights. Some butterflies, such as the speckled wood butterfly, “fight” without physical contact. Males compete for a little sunlit dapple on the forest floor by flying furious circles around each other until one gives up and scrams. No gore, but probably really exhausting.

Pity the protons: Those little particles are under a lot of pressure. Protons’ innards are squeezed harder than any other substance we have measured, a new study finds.

“It’s really the highest pressure we have ever seen,” says physicist Volker Burkert, a coauthor of the study, published in the May 17 Nature. Protons break the pressure record set by neutron stars, the incredibly dense dead stars that can form when a massive star explodes and its core collapses, squeezing more mass than the sun’s into a remnant the size of a city.
The pressure in the proton’s center averages a million trillion trillion times the strength of Earth’s atmospheric pressure, report Burkert and colleagues, from Thomas Jefferson National Accelerator Facility in Newport News, Va. That’s around 10 times the pressure found inside a neutron star. Previously, scientists had theoretically predicted that such pressures might occur inside protons, but the new result is the first experimental proton pressure gauge.

In proton research, the particle’s internal pressure distribution has been a largely unexplored frontier, even though pressure is one of the proton’s fundamental properties. “It’s as important as electric charge or mass,” says physicist Peter Schweitzer of the University of Connecticut in Storrs, but was unknown until now.

Protons are made up of smaller particles including quarks, which are electrically charged, and gluons, which transmit the strong nuclear force that holds protons together (SN: 4/29/17, p. 22). In the center of this ball of particles, Burkert and colleagues report, an intense pressure pushes outward. But this record-breaking outward force is kept in check by an inward pressure from the outer regions of the particle.

This pressure pattern parallels what happens in much larger objects: “In some sense, it’s looking like a star,” says physicist Oleg Teryaev of the Joint Institute for Nuclear Research in Dubna, Russia. Stars also have pressures that push outward in their centers, which counteract the inward pull of gravity.
Protons are held together by the strong force, just as stars are held together by gravity. But the tiny protons are a different beast. So “it’s natural, but it’s not completely trivial” that the two objects would have similarities pressure-wise, Teryaev says.
To quantify the proton’s squeeze, the researchers used data from a particle detector known as CLAS, short for the Continuous Electron Beam Accelerator Facility Large Acceptance Spectrometer, located at Jefferson Lab. In experiments with CLAS, scientists shot electrons at liquid hydrogen, a plentiful source of protons, and watched what happened as electrons interacted with the protons’ constituents and ricocheted away. The new measurement is based on data from 2015 that was analyzed for the first time using a technique that could tease out the proton’s pressure.

The experiment, however, studied the quarks in protons, but not gluons, because the energy of the electrons — 6 billion electron volts — was not enough for the electrons to fully probe the protons. To make their pressure estimate, the researchers assumed that the gluons’ pressure contribution was the same as the quarks’, which is in line with some theoretical predictions.

Future particle accelerators, such as the planned Electron-Ion Collider, would allow for gauging the gluons’ contribution to provide a better estimate of the crushing pressure protons endure.

Green blood is weird enough. But now the first genealogical tree tracing green blood in New Guinea’s Prasinohaema lizards is suggesting something even odder.

These skinks have been lumped into one genus just because of blood color, says biologist Christopher Austin of Louisiana State University in Baton Rouge. Yet they don’t all turn out to be close relatives. Green blood looks as if it arose four separate times in the island’s lizards, he and colleagues propose May 16 in Science Advances.
These lizards do have crimson red blood cells, but that color is overwhelmed by extreme buildups of a green pigment called biliverdin at levels that could kill other animals. Biliverdin forms as the oxygen-carrying hemoglobin molecules break down in dead red blood cells. In humans, biliverdin is converted into the bile that, in excess, causes yellow jaundice. An excess of the biliverdin itself can cause green jaundice. In one case study, levels reaching nearly 50 micromoles of biliverdin per liter of blood were deadly in humans. Yet Austin has found lizards thriving with 714 to 1,020 micromoles per liter (SN: 8/20/16, p. 4).

To figure out how such a peculiar trait evolved, he and colleagues compared segments of DNA and reconstructed the evolutionary history of green-blooded lizards and some close relatives. The greens did not emerge as a single cluster, but were scattered among the reds. The most probable explanation is that green blood, though rare, evolved independently multiple times, he says. The team is now working out the full sequences of lizards’ DNA building blocks and hoping to spot clearer evolutionary clues, such as particular mutations that helped red turn green. He hopes this research eventually will yield insights into human bile disorders.
High but harmless biliverdin hasn’t turned up in the blood of other reptiles, or in mammal and bird blood. Older papers, however, argue for high circulating biliverdin in some sculpins and other fishes in at least two more families, two frogs and insects such as tobacco hornworm caterpillars.
Whether the pigment offers any advantage is still a mystery. When Austin started studying lizards, he wondered if green blood would deter predators. “I tested the hypothesis by eating a few lizards myself and also feeding lizards to native birds and snakes,” he says. “No ill effects.” Now he’s musing that biliverdin might discourage blood parasites such as malaria pathogens.

And the taste of a green-blooded lizard? “Like bad sushi,” he says.

The Elephant Man, novelist Pearl S. Buck and Phoebus, god of the sun, all find their way into science writer Carl Zimmer’s latest book. In She Has Her Mother’s Laugh, Zimmer uses famous moments in history — and Greek mythology — to explain genetics and how researchers have come to understand heredity and try to manipulate it.

Zimmer walks through centuries of exploration, settling into stories of scientists who tried to use simplistic notions of heredity to improve the human race. While investigating inheritance, Francis Galton, who coined the term “eugenics,” noticed that notable men had notable sons. He suggested in 1865 that England’s well-being depended on a national breeding program to produce more talented people. His hereditary utopia would make a terrifying episode of TV’s Black Mirror. Galton’s work launched later efforts in the United States to erase undesirable characteristics through sterilization laws and mental capacity checks of immigrants. Eugenics also fed the Nazis’ notion of a superior race. Zimmer doesn’t shy away from the harmful impact of such research and describes the science that showed the flaws in such discriminatory thinking.
With more than 550 pages, the book covers a lot of ground, from discoveries of inherited diseases like phenylketonuria to mosaics, individuals whose cells are not all genetically identical. In places, Zimmer uses the private lives of public figures to introduce advances in genetics. With so many examples, it’s hard to grasp why he included certain stories. Some parts drag a bit, others zing.
We’re all familiar with Joseph Merrick, the Elephant Man. How researchers came to understand why he was deformed is fascinating. In the early 2000s, scientists discovered that several people with the same disease, now called Proteus syndrome, had mutations in the AKT1 gene important to controlling cell growth. There is current work on a drug to block the gene’s actions. Too late for Merrick, but the work offers hope for people today with the disease.

For some readers, the parts of the book that cover recent research history may feel like familiar walks down memory lane, with added context and details. Zimmer takes us back to research on Neandertals interbreeding with ancient humans (SN: 6/5/10, p. 5), Pima Indians and their high rates of type 2 diabetes, and CRISPR, the prized gene-editing tool (SN: 9/3/16, p. 22). Zimmer describes following CRISPR research as a reporter, witnessing “the beginning of something enormous.”

The book ends with cautionary tales about past attempts to toy with nature to fix environmental problems that turned into ecological disasters. Zimmer also points out future risks of gene manipulation that scientists and ethicists have just begun to consider. The next chapter on heredity, he notes, has as many warning signs as opportunities.

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LEESBURG, Va. — Astronomers watching the 2017 solar eclipse from the ground and from the air witnessed new, tantalizing features of the sun’s outer atmosphere.

Three teams have recently presented their first science results from the Great American Eclipse. Combined, the findings could help disentangle lingering solar puzzles, such as how bursts of plasma leave the sun, why the outer atmosphere, the solar corona, is so well organized and what is the nature of the corona’s magnetic field.
While thousands of eclipse watchers gathered across the country last August armed with special glasses and cameras, solar physicists Adalbert Ding and Shadia Habbal and their colleagues set up a specially designed spectrometer in Mitchell, Ore. (That was one of four sites from which their team monitored the eclipse.) The team had used an earlier version of the instrument, which takes in specific wavelengths of light that can trace different coronal temperatures, to watch a solar eclipse in March 2015 from Svalbard, Norway.
In both 2015 and 2017, the scientists observed evidence of relatively cool blobs of gas embedded in hot plasma in the outer corona. (The sun’s surface simmers at about 6000° Celsius, but its corona roasts at millions of degrees — and no one knows why.) Ding, of the Institute for Optics and Atomic Physics in Berlin, and Habbal, of the University of Hawaii in Honolulu, measured wavelengths of light emitted by atoms and charged particles called ions in the corona, as a proxy for the plasma’s heat.
To the researchers’ astonishment, they saw blobs of plasma during both eclipses that had maintained temperatures as low as 20,000° C embedded within material in the corona that was as hot as 3.7 million degrees Celsius, Ding said at the Triennial Earth-Sun Summit on May 23. “We were very surprised,” Ding says. He thinks the cooler material may be trapped within plasma bubbles and can’t get out. “The stunning thing is that they survive.”
The team also measured solar material’s Doppler shift, or the change in wavelength as the material moved toward or away from Earth. The shifts suggested that the scientists had caught a huge bubble of plasma erupting off the sun’s surface and fleeing out into space in 2015 (SN Online: 6/16/17). At the time, they thought seeing such an explosion, called a coronal mass ejection, was just luck.

If so, their luck held for the 2017 eclipse. The researchers haven’t finished processing all of their data yet, but preliminary results showed uncharged hydrogen and helium atoms fleeing the sun as far out as 3.5 solar radii from the edge of the sun’s bright disk, at speeds of about 600 kilometers per second.

In another talk at the meeting, solar physicist Amir Caspi of the Southwest Research Institute in Boulder, Colo., presented results from a different vantage point: a WB-57F aircraft flying at about 15 kilometers in altitude.

Caspi’s team was trying to see signs of magnetic waves called Alfvén waves rippling through the outer corona. Simulations of the plasma in the corona “lead you to this Velcro-looking thing, a tangled snarled mess,” Caspi said. “In fact, that’s not what we see.” Alfvén waves could smooth out the snarls, which could help explain why the material there is so neatly organized (SN Online: 8/17/17). What’s more, the waves may contribute to the mysterious coronal heating. So Caspi’s colleagues flew telescopes on a pair of NASA’s high-altitude aircraft during the eclipse to look for these waves.
The results were mixed, Caspi admits, in part because the telescopes were not designed for this type of science. NASA originally commissioned them to monitor shuttle launches for issues after the space shuttle Columbia disaster in 2003 (SN: 2/8/03, p. 83).

“Our mission was the first attempt to use them for astronomy,” Caspi says.

The telescopes saw some motion in the corona that could have been waves — or could have been jitter from the planes’ motion. “They’re tantalizing, they’re definitely not random,” Caspi said. “But we don’t know yet whether this is an artifact of the corrections we had to make, or if this is really on the sun.”

The team also captured an image of the corona in infrared wavelengths, which the researchers think is the first image of its kind. Eventually, such infrared measurements could help scientists measure the corona’s magnetic field, which governs most of the corona’s behavior but has never been measured directly (SN Online: 8/16/17).

In another experiment, solar physicist Jenna Samra of Harvard University and her colleagues were on the lookout for certain infrared wavelengths in the corona that were expected to be bright enough to see from the ground.

The team measured five wavelengths, one of which had never been seen before, the team reports in the April 1 Astrophysical Journal Letters. Solar physicist and study coauthor Philip Judge of the High Altitude Observatory in Boulder had predicted in 1998 that those wavelengths, which are especially sensitive to the magnetic field, should be visible in the corona. The results can help plan future observations with the Daniel K. Inouye Solar Telescope, currently under construction in Maui, Hawaii.

Judge and other team members observed the eclipse from Casper, Wyo., and saw some of the same wavelengths (SN Online: 8/21/17), although water in Earth’s atmosphere absorbed some of the light.

Samra, however, observed the eclipse from a plane, a Gulfstream V aircraft at an altitude of 14.3 kilometers. “It was a one-of-a-kind experience. I wouldn’t trade it,” she says. “But in the moment it was terrifying, honestly.”

Fusion may have a dark side. A shadowy hypothetical process called “dark fusion” could be occurring throughout the cosmos, a new study suggests.

The standard type of fusion occurs when two atomic nuclei unite to form a new element, releasing energy in the process. “This is why the sun shines,” says physicist Sam McDermott of Fermilab in Batavia, Ill. A similar process — dark fusion — could occur with particles of dark matter, McDermott suggests in a paper published in the June 1 Physical Review Letters.
If the idea is correct, the proposed phenomenon may help physicists resolve a puzzle related to dark matter — a poorly understood substance believed to bulk up the mass of galaxies. Without dark matter, scientists can’t explain how galaxies’ stars move the way they do. But some of the quirks of how dark matter is distributed within galaxy centers remain a mystery.

Dark matter is thought to be composed of reclusive particles that don’t interact much with ordinary matter — the stuff that makes up stars, planets and living creatures. That introverted nature is what makes the enigmatic particles so hard to detect. But dark matter may not be totally antisocial (SN: 3/3/18, p. 8). “Why wouldn’t the dark matter particles interact with each other? There’s really no good reason to say they wouldn’t,” says physicist Manoj Kaplinghat of the University of California, Irvine.

Scientists have suggested that dark matter particles might ricochet off one another. But the new study goes a step further, proposing that pairs of dark matter particles could fuse, forming other unknown types of dark matter particles in the process.

Such dark fusion could help explain why dark matter near the centers of galaxies is more evenly distributed than expected. In computer simulations of galaxy formation, the density of dark matter rises sharply toward a cusp in the center of a galaxy. But in reality, galaxies have a core evenly filled with dark matter.
Those simulations assume dark matter particles don’t interact with one another. But dark fusion could change how the particles behave, giving them energy that would provide the oomph necessary to escape entrapment in a galaxy’s dense cusp, thereby producing an evenly filled core.

“You can kick [particles] around through this interaction, so that’s kind of cool,” says physicist Annika Peter of the Ohio State University in Columbus. But, she says, dark fusion might end up kicking the particles out of the galaxy entirely, which wouldn’t mesh with expectations: The particles could escape the halo of dark matter that scientists believe surrounds each galaxy.

For now, if fusion does have an alter ego, scientists remain in the dark.

Tropical cyclones don’t move as fast as they used to.

The fierce, swirling storms move 10 percent slower, on average, than they did nearly 70 years ago, a new study finds. Such lingering storms can potentially cause more damage by dumping even more rainfall on land beneath them.

Atmospheric scientist James Kossin examined changes in how quickly tropical cyclones, known as hurricanes in the Atlantic Ocean, moved across the planet from 1949 to 2016. Storms slowed at different rates depending on the region, with the biggest changes seen in the Northern Hemisphere, Kossin reports in the June 7 Nature.
Over that same time period, the average temperature of Earth’s surface rose by about half a degree Celsius. Scientists already predict that average wind speeds will increase in tropical cyclones as ocean waters warm due to global warming (SN: 6/27/15, p. 9). The new study suggests that climate change is also altering how quickly these tropical cyclones travel across land or water.

The effect was even more pronounced as storms moved over land, with those originating in the western North Pacific, such as near Japan, slowing by 30 percent. Storms coming in from the North Atlantic – such as 2017’s Hurricane Harvey — are moving 20 percent slower over land, says Kossin, of the National Oceanic and Atmospheric Administration’s National Centers for Environmental Information in Madison, Wis.
The new study makes an important link between the atmospheric effects of global warming to its effects on tropical cyclones, says atmospheric scientist Christina Patricola of the Lawrence Berkeley National Laboratory in California, who also wrote a commentary that accompanies the new paper. “Tropical cyclones tend to move along with larger-scale [atmospheric] circulation around them,” she says. “Kossin perceptively hypothesized that this overall slowdown would also affect tropical cyclones.”

It’s not clear whether the slowdown will continue into the future, or how it might vary regionally, Patricola says. Most previous work has focused on how climate change will affect the wind speeds of storms rather than how quickly they travel, known as the translation speed. “But in order to have the best information for building resilience to storms, we need to understand these other characteristics,” she says.

The cyclone slowdown is consistent with a weakening in atmospheric circulation in the tropical parts of the planet, a result of global warming, Kossin found. Global warming is also expected to increase how much water vapor the atmosphere can hold, which means storms could accumulate more moisture before releasing it in rainfall.

Slow-moving Hurricane Harvey, which dumped record levels of rain while lingering for days over southern Texas, could be a harbinger of things to come.

Suicide research is undergoing a timing shift, and not a moment too soon. A new breed of studies that track daily — and even hourly — changes in suicidal thinking is providing intriguing, although still preliminary, insights into how to identify those on the verge of trying to kill themselves.

Monitoring ways in which suicidal thoughts wax and wane over brief time periods, it turns out, can potentially strengthen suicide prevention strategies.

Digital technology has made these investigations possible. Smartphone applications alert people to report on suicidal thoughts as they arise in real-world settings. Scientists have traditionally been limited to tracking suicidal thinking over intervals of weeks, months and years, often in research labs and hospitals.

But risk factors that do a decent job of predicting the emergence of suicidal thoughts and acts over the long haul, such as persistent feelings of hopelessness, provide little help in tagging those who will become suicidal in the coming hours and days. Depression, often cited as a main driver of suicide, displays a strong link to suicidal thoughts but not to attempting or completing suicide in the near future.

Despite increasing efforts to combat suicide, U.S. suicide rates steadily rose from 1999 to 2016 (SN Online: 6/7/18). After declining during the 1990s, U.S. suicide rates now roughly equal those of 100 years ago. In recent weeks, the surprising high-profile suicides of designer Kate Spade and chef and television star Anthony Bourdain have attracted more attention to this problem.

“The field of suicide research needs to move away from its obsession with long-term risk studies,” says psychologist David Klonsky of the University of British Columbia in Vancouver. A better understanding of how particular suicidal thoughts play out in daily life will lead to the identification of the most telling warning signs of impending suicide attempts, Klonsky predicts. Current theories focus on a range of potential factors that transform suicidal thoughts into life-ending actions, including feeling like a burden to others and suffering from unrelenting pain and hopelessness (SN: 1/9/16, p. 22).

Researchers can’t yet pinpoint suicide alarms for specific groups of people. That makes it even more vital for people contemplating suicide to contact suicide hotlines, psychotherapists and friends for help, Klonsky says. (To reach the National Suicide Prevention Lifeline, call 1-800-273-TALK (8255).)

The rise of real-time, digital monitoring holds promise for giving clinicians a heads-up as to who is in the most immediate danger of acting on suicidal thoughts. A handful of studies published since 2009 have found that thoughts of suicide often appear rapidly in individuals with past suicide attempts, and can vary dramatically from hour to hour.

A team led by psychologist Evan Kleiman of Harvard University has taken digital monitoring a step further. The researchers recruited 51 adults from online forums related to suicide and self-harm and 32 adults hospitalized at a Boston psychiatric facility for recent suicide attempts or severe suicidal thoughts. Volunteers carried smartphones that prompted them four times daily, between four and eight hours apart, to rate the intensity of their current desire to kill themselves, their intention to carry out the act and their ability to resist suicidal urges. Those in the online group provided responses for 28 consecutive days. Hospitalized participants provided responses until they were discharged, a period that typically lasted one to two weeks.

The same five patterns of suicidal thinking appeared in both groups, Kleiman’s team reports in a paper scheduled for publication later this year in Depression and Anxiety. One of those profiles may be associated with the greatest risk for trying to kill oneself in the future, the researchers say.
Some individuals reported, on average, low levels of suicidal thoughts that either stayed constant, varied moderately or fluctuated greatly throughout the day. Others reported severe suicidal thoughts that varied either a little or a lot from one report to the next.

Among past-year attempters, suicide tries in the month before the study clustered among those reporting severe suicidal thoughts with few fluctuations. No such association appeared in the hospitalized group, probably because most of those with each profile had been admitted shortly after suicide attempts. Following these people for a longer period, after hospital discharge, might yield a link between a specific profile of suicidal thinking and previous or new suicide attempts.

Kleiman is now participating in a similar study, directed by Harvard psychologist Matthew Nock, of 300 adults and 300 adolescents with histories of suicide attempts who will be monitored for six months after discharge from psychiatric facilities. Participants will respond to smartphone questions and wear sensors that monitor sleep and activity cycles. “Some people have difficulty recognizing how distressed they are in the moment, so we need to capture distress with nonverbal measures,” Kleiman says. By identifying these individuals, clinicians could help them to recognize physical signs of distress in themselves and devise a plan to get help when such signs occur, Klonsky adds.

A related proposal holds that at least two forms of suicidal thinking, one related to spikes in distress, exist and demand closer study in smartphone studies. Psychiatrist Maria Oquendo of the University of Pennsylvania’s Perelman School of Medicine and colleagues suspect that the first consists of sudden bursts of suicidal thoughts following stressful experiences, possibly rooted in stress sensitivity due to child abuse or other early traumas. The second is linked to a consistently depressed mood that likely leads to carefully planned suicide attempts. Oquendo and her colleagues have found evidence for these two types of suicidal thinking in surveys of more than 6,700 U.S. college students.

Stress, or the lack of it, might play a role in some or all of the patterns of suicidal thinking identified by Kleiman’s group. Sleep and activity data in the team’s upcoming study may provide an indirect look at how stress affects suicidal thoughts.

Another digital-monitoring study in the works is that of psychologist Catherine Glenn of the University of Rochester in New York. She is currently assembling a smartphone-and-sensor study that will track 50 teenagers hospitalized following suicide attempts for one month after discharge. “It’s still unclear how much suicidal thoughts fluctuate over short periods of time, especially in youth,” Glenn says.

Despite its promise, digital monitoring of people at risk for suicide only works if people respond to repeated surveys. Consider that U.S. Army soldiers who refused to answer a survey question about the duration of their suicidal thoughts were especially likely to try later to kill themselves. A team led by Harvard psychologist Matthew Nock reported that finding in the February Journal of Abnormal Psychology. Rochester’s Glenn adds that some teens recently released from psychiatric facilities go offline for a couple of days before being hospitalized again for a suicide attempt.

“Suicide is such a complicated area of study,” Glenn says.

Time is out of joint on Venus. The planet’s thick air, which spins much faster than the solid globe, may push against the flanks of mountains and change Venus’ rotation rate.

Computer simulations show that the thick Venusian atmosphere, whipping around the planet at 100 meters per second, exerts enough push against a mountain on one side and suction on the other side to speed the planet’s rotation rate by about two minutes each Venus day, according to a study in Nature Geoscience June 18.
That’s not much, considering that the planet rotates just once every 243 Earth days. By comparison, Venus’ atmosphere rotates about once every four Earth days. Precise measurements of the planet’s rotation rate have varied by about seven minutes, however. The push and pull of the air over the mountains could help explain the mismatch, with some other force — possibly the gravitational influence of the sun — slowing the planet’s spin back down.
The simulations by UCLA planetary scientist Thomas Navarro and colleagues are the first to account for a 10,000-kilometer-long wave in Venus’ cloud tops
, spotted in 2015 by the Japanese space agency’s Akatsuki spacecraft (SN: 2/18/17, p. 5) . Similar waves are launched into the atmosphere on Earth when air flows over a mountain, but they normally dissipate quickly as opposing winds break them up. Venus’ atmosphere rotates so much faster than the planet and in such a uniform direction that the waves could persist for a long time.
“This work is very interesting,” says planetary scientist Tetsuya Fukuhara of Rikkyo University in Tokyo, one of the researchers who discovered the atmosphere wave. The work helps explain where the wave comes from and addresses how Venus’ surface features affect the atmosphere, “which is the most important issue in the Venus atmospheric science.”

More detailed measurements of Venus’ rotation, possibly taken with a future lander (SN: 3/3/18, p. 14), could eventually help reveal details of Venus’ interior, such as the size of its core.

“Venus is the closest thing to Earth that we know of,” Navarro says, and yet its hot, thick, toxic atmosphere makes it utterly alien. “We’d like to know what’s inside.”

MADISON, Wis. — Giving children with autism a healthier mix of gut bacteria as a way to improve behavioral symptoms continued to work even two years after treatment ended.

The finding may solidify the connection between tummy troubles and autism, and provide more evidence that the gut microbiome — the collection of bacteria and other microbes that live in the intestines — can influence behavior.

“It’s a long way from saying there’s a cure for autism,” says Michael Hylin, a neuroscientist at Southern Illinois University in Carbondale who was not involved in the work. “But I think it’s a promising approach. It’s one that’s worthwhile.”

Children with autism spectrum disorders often have gastrointestinal problems. In previous studies, environmental engineer Rosa Krajmalnik-Brown of Arizona State University in Tempe and colleagues discovered that children with autism had fewer types of bacteria living in their guts than typically developing children did. And many of the kids were missing Prevotella bacteria, which may help regulate immune system actions. The researchers wondered whether altering the children’s cocktail of gut microbes to get a more diverse and healthier mix might help fix both the digestive issues and the behavioral symptoms associated with autism.
In a small study of 18 children and teenagers with autism, the scientists gave kids fecal transplants from healthy donors over eight weeks. During and two months after the treatment, the kids had fewer gastrointestinal problems, including diarrhea, constipation, abdominal pain and indigestion, than before the therapy. Autism symptoms, such as hyperactivity, repetitive actions and irritability, also improved and seemed to be getting even better at the end of the trial than immediately after treatment ended, the team reported last year in Microbiome. But no one knew whether the improvements would last.

Krajmalnik-Brown announced the results of a two-year, follow-up study July 10 at the Beneficial Microbes Conference. The children had kept many of the Prevotella and other beneficial bacteria gained during treatment. And the diversity of bacteria in the children’s guts was even greater two years later than it was two months after the therapy ended, Krajmalnik-Brown said.

Some of the children’s stomach troubles had worsened slightly. But on average, scores on a gastrointestinal-symptoms scale were still more than 60 percent better than before kids received the transplants. The real surprise was that the kids’ autism symptoms continued to lessen two years after the therapy ended. Still, the study was small. “Don’t try this at home,” Krajmalnik-Brown cautioned.

The children were ages 7 to 16 when the study started. Ideally, treatment would begin at younger ages, Krajmalnik-Brown said, but the researchers have not gotten approval to conduct the research in younger children.

Next, the scientists need to make sure that the improved behavioral symptoms are really due to fecal transplants. The team will put the idea to the test in a study of the therapy in adults with autism.