An orbital oopsie has led to new proof of Albert Einstein’s physics prowess.

In 2014, two satellites intended for Europe’s Galileo network, the equivalent of the United States’ GPS network, were placed into orbit incorrectly, causing them to travel around Earth in ellipses rather than circles. That wasn’t ideal for the satellites’ originally intended navigational use, but scientists realized the wayward satellites were perfect for another purpose: testing Einstein’s theory of gravity, the general theory of relativity.

According to general relativity, gravity affects not just space, but also time. The deeper within a gravitational field you are, the slower time passes (SN: 10/17/15, p. 16). So a clock at a higher altitude will tick faster than one closer to Earth’s surface, where Earth’s gravity is stronger. The satellites’ orbital mishap allowed the most precise test yet of this effect, known as gravitational redshift, two teams of scientists report in a pair of papers in the Dec. 7 Physical Review Letters.

As the two misplaced satellites move in their elliptical orbits, their distance from Earth periodically increases and decreases by about 8,500 kilometers. Using the precise atomic clocks on the satellites, the scientists studied how that altitude change affected the flow of time. The clocks sped up and slowed down by tiny fractions of a second as expected, agreeing with the predictions of general relativity within a few thousandths of a percent, the teams report.

Poop contains a lot of valuable scientific information. Researchers can monitor microbes, track enzyme activity or hunt for DNA to gather clues about overall health.

There’s so much one can learn from the waste product that microbiologist Aadra Bhatt at the University of North Carolina at Chapel Hill decided there should be a word for that research — something in the same vein as “in vivo” (research done in living animals) and “in vitro” (research done in a petri dish).

After some linguistic digging, she and two colleagues settled on “in fimo.” The term comes from fimus, one of several Latin words for manure or excrement. Their choice won out over the more obvious option of “in feces” because the word feces doesn’t have the same rich scatological legacy — originally it referred to the dregs in a wine cask, Bhatt says.

She and her colleagues, while already using in fimo at meetings and seminars, published their argument online December 13 in Gastroenterology. Compared with the laborious process of pulling together a scientific paper, coming up with this term was “delightful — and it wasn’t particularly drawn out,” Bhatt says. She hopes the word catches on and gains a place in the lexicon for poopetuity.

SEATTLE — Astronomers have spotted a second repeating fast radio burst, and it looks a lot like the first. The existence of a second repeating burst suggests there could be many more of the mysterious signals in the cosmos.

The burst, called FRB 180814.J0422+73, is one of 13 newly discovered fast radio bursts, or FRBs — brief, bright signals of radio energy that come from distant galaxies. The FRBs were detected over a few weeks last year by the Canadian Hydrogen Intensity Mapping Experiment, or CHIME, in British Columbia. Astronomers reported the discoveries at a meeting of the American Astronomical Society on January 7 and in the Jan. 9 Nature.
Most such bursts erupt once, last for a few milliseconds, and are never seen again. So astronomers have puzzled over what causes them for years (SN: 8/9/14, p. 22).

“If you have something that flashes for a millisecond in the sky, and there’s nothing that happens for many years, it’s really hard to study,” says astronomer Shriharsh Tendulkar of McGill University in Montreal, a member of the CHIME team.

But then in 2016, astronomers discovered the first repeating FRB when they realized that a series of bursts all came from a single source, called FRB 121102 (SN: 4/2/16, p. 12). Astronomers tracked the signal to its host galaxy (SN: 2/4/17, p. 10) and determined it was coming from an extremely magnetic environment, such as the region surrounding a black hole (SN: 2/3/18, p. 6). Researchers didn’t know if FRB 121102’s repeating signal was unique. Of the more than 60 FRBs detected, no other was known to repeat — until now. Having spotted a second one, scientists are searching for more.

“Imagine you saw a unicorn,” Tendulkar says. “Then suddenly you discover another one. You know now there is a population of these. There is hope for discovering a lot more.”
The CHIME team detected the first of the repeating FRB signals on August 14, with four more coming over the next two months from the same spot on the sky. It wasn’t until the third burst, on September 17, that the team realized they might have a repeater, Tendulkar says.

“Somebody pointed out, hey look, these three bursts seem to have the same properties,” he says. “Everybody got really excited.”

Calculations show that the new repeater is about 1.6 billion light-years away. The CHIME team also saw an odd similarity between the two known repeating bursts. Most FRBs are just a sharp blip, akin to a single note being played on a trumpet. But some of the individual bursts in both repeaters were made up of multiple sub-bursts that descended in frequency, like the “wah wah wah wah” of a sad trombone.

“We’ve seen this in 121102, and we can’t explain it,” says astronomer Emily Petroff of ASTRON, the Netherlands Institute of Radio Astronomy, who was not involved in the new work. “Up until now we’ve only had the one repeater, and it’s given us more questions than answers.” But the fact that both repeaters behave similarly could suggest they have similar origins, she says.

Astronomers may have already caught a third repeating burst, too. FRB 110523, discovered in 2015, has some similar features to the first known repeating FRB, so it was worth checking to see if it also repeats, said astronomer Allison McCarthy of the University of Alabama in Tuscaloosa.

Together with Andrew Seymour of the Green Bank Observatory in West Virginia, McCarthy analyzed more than 41 hours of observations of FRB 110523 taken at the Arecibo Observatory in Puerto Rico. They found one potential repeat burst, McCarthy reported January 9 in a poster at the AAS meeting, but they’re not declaring victory just yet. “It wasn’t strong enough for us to be very sure we had detected one,” McCarthy said, adding that they’re about 60 percent certain. “But it’s still a promising candidate.”

Astronomers’ theories for what causes FRBs are almost as numerous as known FRBs themselves. At one point, astronomers even considered the idea that FRBs could be signals from intelligent aliens. But it’s unclear if the repeating bursts and single bursts both come from the same kinds of sources, or even if one-offs might also repeat if watched for long enough.

“It’s the wild, wild west out there,” Tendulkar says. “We have tantalizing clues, but it’s hard to make definitive conclusions.”

CHIME is likely to catch a lot more of these fast radio bursts. The telescope was still being tested when it caught the 13 new ones, so was not operating at peak performance. “They just barely turned on the telescope,” Petroff says, “and they’re already finding things.”

SAN FRANCISCO — Seizures during sleep can scramble memories — a preliminary finding that may help explain why people with epilepsy sometimes have trouble remembering.

The sleeping brain normally rehashes newly learned material, a nocturnal rehearsal that strengthens those memories. Neuroscientist Jessica Creery and her colleagues forced this rehearsal by playing certain sounds while nine people with epilepsy learned where on a screen certain pictures of common objects were located. Then, while the subjects later slept, the researchers played the sounds to call up some of the associated memories.

This sneaky method of strengthening memories, called targeted memory reactivation, worked as expected for five people who didn’t have seizures during the process. When these people woke up, they remembered the picture locations reactivated by a tone better than those that weren’t reactivated during sleep, said Creery, of Northwestern University in Evanston, Ill. She presented the research March 25 at the annual meeting of the Cognitive Neuroscience Society.

The opposite was true, however, for four people who had mild seizures, detected only by electrodes implanted deep in the brain, while they slept. For these people, memory reactivation during sleep actually worsened memories, making the reactivated memories weaker than the memories that weren’t reactivated during sleep. The combination of seizures and memory reactivation “seems like it’s actually scrambling the memory,” Creery says, a finding that suggests that seizures somehow accelerate forgetting.

A few months back, a new storefront appeared in my small Oregon town. Its shelves were packed with tinctures, jars of salve, coffee beans, bath bombs — even beard oil. This motley collection shared a single star ingredient: CBD.

Produced by the cannabis plant, CBD is the straitlaced cousin of marijuana’s more famous component — the THC that delivers a mind-swirling high. CBD, or cannabidiol, has no such intoxicating effects on the mind. Yet the molecule has captured people’s attention in a profound way, sold as a remedy for pain, anxiety, insomnia and other ailments — all without the high.

That neighborhood shop, CBD Scientific, is far from alone in its efforts to sell people on the benefits of CBD, which is found in both marijuana and hemp, two versions of the Cannabis sativa plant. CBD is popping up in products in pet stores, coffee shops and the health and beauty sections of mainstream grocery stores. It’s even being brewed into beer. I left the shop with a $5 bottle of water infused with “5,000,000 nanograms” of CBD.

So far, messages of CBD’s purported health benefits come from people trying to sell CBD products — not from scientists, says Margaret Haney, a neurobiologist who directs the Marijuana Research Laboratory at Columbia University. A gaping chasm separates the surging CBD market and the scientific evidence backing it. While there are reasons to be excited about CBD, the science just isn’t there yet, Haney says.
Scientists still don’t know all of the targets CBD hits in the human body, nor what effects it may have, if any. With the exception of tests in people with rare forms of epilepsy, large studies that compare CBD with placebos in people are rare. Much of the existing research was done with cells in the lab or in lab animals, with results that don’t necessarily translate to people.

And there’s always the chance that for some people, CBD’s magic is made not by the compound itself but by a powerful placebo effect; people who expect good outcomes are more likely to see benefits.

Researchers are stepping into the void, lured by promising early data. Small trials are under way looking at the effect of CBD on anxiety, pain, opioid addiction, depression and other health problems. National Institutes of Health funding for CBD studies went from zero in 2014 to an estimated $16 million in 2018.
“We’re very interested in CBD,” says Susan Weiss, director of the Division of Extramural Research at the National Institute on Drug Abuse in Bethesda, Md. Still, she urges caution to people eager to try CBD. Because of lax oversight, there’s no telling what’s inside many of those tinctures, oils, rubs and foods for sale online and in stores. “A lot of the products that people are taking may not be what they think,” she says.

Despite the risks and warnings, it seems safe to say that the collective fascination with CBD isn’t going to wear off anytime soon. “People think it’s great for everything,” says cognitive neuroscientist Kent Hutchison of the University of Colorado Boulder. That can’t possibly be true, he says. “But I do think it’s going to be great for some things. We just need to figure out what those things are.”

Mystery molecule
Each morning, Samantha Montanaro of Portland, Ore., drops a CBD tincture under her tongue. “I’m kind of testing out my own body with this,” she says. “I’m finding that it really helps with anxiety and stress.”

Montanaro isn’t alone; CBD testimonials are increasingly easy to find. In 2016, Montanaro, now 35, cofounded Tokeativity, a global cannabis community for women. Back then, “CBD wasn’t even a thing,” she says. But the first sparks of the CBD movement caught fire fast. “It’s been pretty crazy to watch how things have evolved,” she says. Some bullish analysts predict that the CBD market in the United States will balloon from hundreds of millions of dollars in 2018 to almost $20 billion by 2022.

Ziva Cooper directs UCLA’s Cannabis Research Initiative and fields a lot of questions about CBD. Her answers invariably disappoint. “When I tell [people] we don’t have very much evidence in people, they’re actually surprised,” she says. When it comes to CBD’s benefits, “there’s actually very little out there to hang our hats on.”

The one exception is for rare forms of childhood epilepsy. Neurologist Elizabeth Thiele of Massachusetts General Hospital in Boston had a young patient who was having over 100 seizures a day. After other treatments had failed, the boy’s parents began searching for a source of CBD oil, which they desperately wanted to try after learning about promising early results in animals. The family flew to England, so the boy could try the CBD formulation made by GW Pharmaceuticals. The child’s results, Thiele says, were remarkable. After a week of CBD, his daily seizures had fallen to single digits.
That result ultimately led to clinical trials, one of which included 171 people, mostly children, with Lennox-Gastaut syndrome, a rare and severe seizure disorder. In addition to their normal medication, half of the participants got doses of CBD that were rigorously tested and standardized by the drug’s maker. The other half received their regular treatment plus a placebo. After 14 weeks, the people taking CBD saw a median drop in monthly seizure frequency of about 44 percent; seizures in people who took the placebo dropped almost 22 percent. Thiele and her colleagues published those results in March 2018 in the Lancet.

Side effects were manageable, the researchers found. Diarrhea, sleepiness, poor appetite and vomiting were more likely to occur in the people who took CBD than in those who got the placebo. Along with results from several other trials, those data were strong enough to prompt the U.S. Food and Drug Administration to approve the CBD drug, called Epidiolex, last June.
Despite rigorous testing of Epidiolex, big gaps in knowledge on how the drug works in epilepsy remain. Researchers don’t know how CBD tames seizures. Because the molecule comes from cannabis, the early assumption was that CBD latches onto the same chemical receptors that THC connects to, one primarily in the brain and one mainly on immune cells. It turns out, however, that CBD doesn’t seem to hit either of those receptors.

Instead, studies in rats and mice point to two different targets. One, called TRPV1, is known to play a role in pain sensation and maybe epilepsy, too. The other, called GPR55, might change the activity level of nerve cells in the brain, a feat that may be behind CBD’s antiseizure power.

Scientists also don’t know whether CBD keeps working year after year. For some of Thiele’s patients, CBD seems to still be effective after five years of taking the drug, even allowing them to taper off some of their other medications, she says. But data from 92 other patients, presented in December at the American Epilepsy Society’s annual meeting, suggest that CBD’s benefits can start to fade after about seven months on the drug. About a third of the people in the study needed a dose increase after their CBD doses became less effective, researchers from Tel Aviv Sourasky Medical Center reported.

Research on CBD and other ailments lags way behind the epilepsy work. Early experiments, mostly on lab animals but some in small numbers of people, suggest that CBD might fight anxiety, ease schizophrenia symptoms and address pain.

One example: Healthy men who took CBD before a stressful public speaking task were calmer than those who took a placebo, researchers reported in October in the Brazilian Journal of Psychiatry. But only the 15 men who received doses of 300 milligrams were more relaxed. The 27 who took less or more CBD didn’t see benefits. Other types of studies with people, and studies of mice and rats, have turned up antianxiety effects, too. But most of these studies looked at single doses of CBD, not consistent use.

Early evidence of CBD’s promise against schizophrenia comes from a trial of 88 people with the disorder. After six weeks, people who had received a big daily dose of CBD (1,000 milligrams a day) in addition to their normal medication had more improvements in certain symptoms when compared with people who received a placebo. Those results hint that CBD might be a new type of drug for schizophrenia, researchers wrote in March 2018 in the American Journal of Psychiatry.

Studies in lab animals suggest that CBD may help relieve chronic pain. A study appearing in 2017 in Pain found that CBD could block osteoarthritis pain and nerve damage in rats. Hard data for humans are harder to find, but anecdotes abound. Pain clinician Kimberly Mauer of Oregon Health & Science University in Portland and colleagues at the OHSU Comprehensive Pain Center have seen an uptick in patients who say they’re taking CBD. Their experiences are mixed, she says: “About half the patients say they get some benefit, and about half say they didn’t notice anything.”

No easy access
To answer the many outstanding questions about CBD’s effects, scientists need access to the compound. But a complex web of U.S. regulations makes that difficult. CBD is subject to rules from both the FDA and the U.S. Drug Enforcement Administration. CBD produced by the marijuana plant remains on the DEA’s list of the most restrictive class of drugs, Schedule 1, alongside LSD, ecstasy and other drugs deemed to have no accepted medical use and high potential for abuse. Access restrictions on industrial hemp, and by extension, the CBD that comes from hemp, were eliminated in the 2018 Farm Bill, signed into law in December. However, regardless of its provenance, CBD is still subject to FDA regulations, as well as any regulations imposed by states.
“As easy as it’s gotten for the average person to go legally to buy recreational marijuana and consume it in many states, it’s gotten harder for scientists,” says Haney at Columbia. One of the few approved sources of CBD is a government-sanctioned cannabis facility at the University of Mississippi in Oxford. After she gets the CBD she needs for her studies, Haney is required to meticulously account for every milligram. “I have a gun safe in a locked room that I get into with my fingerprints to store both cannabidiol and marijuana.”

With those restrictions, many scientists just can’t do the studies they want, Hutchison says. “The whole thing is a little bit crazy. People can sell it everywhere, but it’s very difficult for scientists to study its effects in humans.”

Hutchison and colleagues have figured out a legal work-around that doesn’t require researchers to obtain supplies of CBD. The team is avoiding the government-grown cannabis, which can be quite different from the products in circulation, by testing the effects of the cannabis products that people are actually using. To do this, the researchers created a mobile pharmacology lab they call the CannaVan. The tricked-out Dodge contains equipment to study people after they’ve taken a product containing CBD (or THC) that they bought themselves. The researchers are currently collecting data on CBD’s effects on anxiety and pain.
Buyer beware
FDA rules say that CBD cannot be legally added to food and sold across state lines, sold as a dietary supplement or marketed with claims of treating diseases. But aside from sending some warning letters, the FDA has, so far, let the marketplace run uninhibited. (Some local health authorities, however, are beginning to flex their might, warning restaurants in New York City, for instance, to take CBD off the menu.)

Overall, no one really knows what’s inside the bottles, rubs and coffees for sale. A study published in 2017 in JAMA gives a sense of the problem. Researchers ordered and tested 84 products sold online in 2016 as CBD-containing products. Of those, only 26 were labeled accurately (containing CBD within 10 percent of the claimed amount); 36 of the products had more CBD than their labels said; and 22 products had less. The researchers also found THC in 18 of the 84 samples.
Sophie Cloyd is a 30-year-old manager for the CBD company Ablis of Bend, Ore. She is also pregnant. I met her recently at a ski lodge, where she was offering beverage tastes and describing tinctures, oils and lotions. CBD, she says, has helped her manage this pregnancy, her second. She was prescribed the anti-nausea drug Zofran early in her pregnancy, but “the research on Zofran scared me more than the lack of research on CBD,” she says.

Ablis, which makes CBD-infused fizzy drinks and other products, currently gets purified CBD from Colorado, Cloyd says. When the CBD arrives, the company sends it to an independent lab to confirm that it has the right amount of CBD, no pesticides and no THC. But not all CBD sellers test their products.

An unexpected THC dose might not be enough to get a user high, but it could still be a problem, as news reports have begun to point out. To ease his pain from psoriatic arthritis, a school bus driver in Beaverton, Ore., had been taking a daily dose of CBD oil. In early 2018, he failed a periodic drug test with high THC levels, which caused him to lose his job, Portland news channel KATU reported. Even seemingly small amounts of THC can build up in the body with repeated use.

A product might contain even worse surprises. Between December 2017 and January 2018, for example, 52 people fell ill in Utah, with symptoms such as hallucinations, vomiting and seizures, after taking what they thought was CBD. It turned out that the products, many labeled “Yolo CBD oil,” contained a synthetic cannabinoid, and it had poisoned them.

Even if product labels were always accurate, people have no idea of the correct dose of CBD (assuming the right dose would be effective). “You see it marketed in doses like 10 milligrams,” Hutchison says. “Well, 10 milligrams probably does nothing.” For comparison, people who participated in one Epidiolex study took 20 milligrams per kilogram of body weight. To reach that daily dose, I’d need to chug 254 bottles of that 5 million nanogram CBD water I bought — at a cost of $1,270.

Haney makes the same point: “You’re not getting anything resembling an effective dose when you get CBD added to your coffee, or you buy a mint with a little bit of CBD in it,” she says.

There’s even less known about CBD products that you rub on your skin. Scientists don’t know that CBD in creams, oils and ointments actually makes it into the body. “I’m not convinced that anything you’re rubbing on your body with CBD is even getting through,” Haney says.
At its heart, the trouble is that most CBD use isn’t backed up by science, Haney says. “I am not against CBD,” she says. In fact, she is about to start a study looking at CBD to treat nerve pain due to chemotherapy in cancer patients. “But I don’t like marketers determining what it’s good for and what it’s not.”

Hype run amok isn’t anything new, says Mauer, the OHSU pain doctor. Consumers try lots of things before the science is definitive — keto diets, for instance, or vitamin D supplements (SN: 2/2/19, p. 16). And even if it turns out that the chemical doesn’t work, the placebo effect might be enough to help reduce symptoms.

So far, the science on CBD isn’t mature enough to weigh in, one way or another. But judging by the number of studies and clinical trials under way, this nascent research field is growing up fast, seeking to quickly fill the space between the science and what people want to know.

This research boom heartens Montanaro. Her message to the scientific community: “I would encourage curiosity,” she says. “I’m not a doctor, and I’m not a scientist, but I certainly know my own body,” and she says that CBD helps her. From her perspective, science has got some catching up to do.

This story appears in the March 30, 2019 issue of Science News with the headline, “The Allure of CBD: People seek health benefits despite lack of evidence.”

Just beyond the tip of the Antarctic Peninsula lies an iceberg graveyard.

There, in the Scotia Sea, many of the icebergs escaping from Antarctica begin to melt, depositing sediment from the continent that had been trapped in the ice onto the seafloor. Now, a team of researchers has embarked on a two-month expedition to excavate the deposited debris, hoping to discover secrets from the southernmost continent’s climatic past.

That hitchhiking sediment, the researchers say, can help piece together how Antarctica’s vast ice sheet has waxed and waned over millennia. And knowing how much the ice melted in some of those warmest periods, such as the Pliocene Epoch about 3 million years ago, may provide clues to the ice sheet’s future. That includes how quickly the ice may melt in today’s warming world and by how much, says paleoclimatologist Michael Weber of the University of Bonn in Germany.
Weber and Maureen Raymo, a paleoclimatologist at Lamont-Doherty Earth Observatory in Palisades, N.Y., are leading the expedition, which set sail on March 25.

“By looking at material carried by icebergs that calved off of the continent, we should be able to infer which sectors of the ice sheet were most unstable in the past,” Raymo says. “We can correlate the age and mineralogy of the ice-rafted debris to the bedrock in the section of Antarctica from which the bergs originated.”
Icebergs breaking off from the edges of Antarctica’s ice sheet tend to stay close to the continent, floating counterclockwise around the continent. But when the bergs reach the Weddell Sea, on the eastern side of the peninsula, they are shunted northward through a region known as Iceberg Alley toward warmer waters in the Scotia Sea.

Because so many icebergs from all around the continent converge in one region, it is the ideal place to collect sediment cores and take stock of the debris that the bergs have dropped over millions of years.

“That area in the Scotia Sea is so exciting, because it’s a focus point between South America and the Antarctic Peninsula where the currents flow through, and there are a lot of icebergs,” says Gerhard Kuhn, a marine geologist at the Alfred Wegener Institute in Bremerhaven, Germany. “You get a picture of more or less [all of] Antarctica in that area,” says Kuhn, who has studied the region but is not aboard the current cruise.
The expedition, known as leg 382 of the International Ocean Discovery Program, plans to drill at six different sites in the Scotia Sea. At three sites, the team plans to penetrate about 600 meters into the seafloor. “That would likely bring us back to the mid-Miocene, which could translate into 12 million to 18 million years back in time,” Weber says.

At another site, the team plans to drill even deeper, 900 meters, to go further back in time, in hopes of finding sediments that date to the opening of the Drake Passage about 41 million years ago. That passage, a body of water that now lies between South America and Antarctica, opened a link between the Atlantic and Pacific oceans and may have played a role in building up Antarctica’s ice sheets at different times in its history.

A graveyard turned crystal ball
How much a melting Antarctica might have contributed to global sea-level rise following the last great ice age, which ended about 19,000 years ago, has been a subject of debate. Seas rose by about 130 meters from 19,000 to 8,000 years ago, Weber says, and much of the melting happened in the northern hemisphere.

But Antarctica may have played a larger role than once thought. In a study published in Nature in 2014, Kuhn, Weber and other colleagues reported that ice-rafted debris from that time period, as recorded in relatively short sediment cores from Iceberg Alley, often occurred in large pulses lasting a few centuries to millennia. Those data suggested that the southernmost continent was shedding lots of bergs much more quickly during those times than once thought.

Now, the researchers want to see even further into the past, to understand how quickly Antarctica’s ice sheet might have melted during even warmer periods, and how much it may have contributed to episodes of past sea-level rise.

The new drilling expedition targets several periods when the climate is thought to have warmed dramatically. One is a warm period in the middle Pliocene about 3.3 million to 3 million years ago, when average global temperatures were 2 to 3 degrees warmer than today; another is the ending of an older ice age about 130,000 years ago, when sea levels rose by about 5 to 9 meters.

Such periods may serve as analogs to the continent’s future behavior due to anthropogenic global warming. Currently, global average temperatures on Earth are projected to increase by between about 1.5 degrees and 4 degrees Celsius relative to preindustrial times, depending on greenhouse gas emissions to the atmosphere over the next few decades (SN: 10/22/18, p. 18).

“The existing [ice core] record from Iceberg Alley taught us Antarctica lost ice through a threshold reaction,” Weber says. That means that when the continent reached a certain transition point, there was sudden and massive ice loss rather than just a slow, gradual melt.

“We have rather firm evidence that this threshold is passed once the ice sheet loses contact with the underlying ocean floor,” he says, adding that at that point, the shedding of ice becomes self-sustaining, and can go on for centuries. “With mounting evidence of recent ice-mass loss in many sectors of West Antarctica of a similar fashion, we need to be concerned that a new ice-mass loss event is already underway, and there is no stopping it.”

For 40 years, they’ve held the front line in Florida’s fight against mosquito-borne diseases. And it turns out that the chickens standing sentinel in cities, marshes, woodlands and residential backyards are clucking good at their job.

Last year, chickens in 268 coops in over a third of Florida’s counties provided scientists weekly blood samples that revealed whether the birds had been bitten by mosquitoes carrying West Nile virus or the Eastern equine encephalitis or St. Louis encephalitis viruses.
If a chicken’s blood tests positive for antibodies to one of those viruses, authorities know that the pathogen is circulating. And if enough birds have the antibodies, state officials can ratchet up mosquito-killing measures such as pesticide spraying to help halt disease spread.

The sentinel chicken surveillance programs are “a really good way of monitoring” for certain virus activity, says Thomas Unnasch, a biologist who studies vector-borne diseases at the University of South Florida in Tampa. The birds “are sampling literally hundreds or thousands of mosquitoes every day,” he says. (The chickens can’t keep tabs on dengue or Zika; the mosquitoes carrying those viruses prefer to bite people rather than birds.)
In 2018, 833 chickens tested positive for West Nile virus antibodies in Florida, but only 39 people did, according to data from the state’s health department. For Eastern equine encephalitis virus, 154 chickens tested positive in 2018, compared with only three people.
Chickens that test positive for the viruses being surveyed don’t transmit them, and people don’t either. Both are considered “dead-end hosts,” meaning that the viral concentration in the blood doesn’t get high enough to infect another mosquito after it bites. Infected cardinals, robins and other backyard birds are the animal reservoirs that help keep the three viruses spreading in the area.
Sentinel chickens, by detecting where and when disease-carrying mosquitoes are buzzing, are also providing valuable data on how a virus can spread. Data from 2005 to 2016 revealed that Eastern equine encephalitis virus is active year-round in the Florida panhandle, making the area a source from which the virus moves elsewhere in the state and along the eastern United States, Unnasch and his colleagues report online March 11 in the American Journal of Tropical Medicine and Hygiene.

In people, the viral diseases monitored by the chickens are relatively rare, but can be deadly. The chickens don’t get especially sick, though. “You don’t usually see any symptoms at all,” Unnasch says.

Any chicken whose blood tests positive for the antibodies is removed from the coops since that bird can no longer alert authorities to a new infection. For these chickens, retirement may be spent on a farm, with school or 4-H clubs, or in a backyard coop, depending on the county. The sentinel chicken programs are ready with replacements, raising chicks to supply new birds to signal “where we have a threat to human health,” Unnasch says.

It took just a 9-volt battery and a little brain zapping to turn science writer Sally Adee into a stone-cold sharpshooter.

She had flown out to California to test an experimental DARPA technology that used electric jolts to speed soldiers’ sniper training. When the juice was flowing, Adee could tell. In a desert simulation that pit her against virtual bad guys, she hit every one.

“Getting my neurons slapped around by an electric field instantly sharpened my ability to focus,” Adee writes in her new book, We Are Electric. That brain-stimulating experience ignited her 10-year quest to understand how electricity and biology intertwine. And she’s not just talking neurons.
Bioelectricity, Adee makes the case, is a shockingly under­explored area of science that spans all parts of the body. Its story is one of missed opportunity, scientific threads exposed and abandoned, tantalizing clues and claims, “electroquacks” and unproven medical devices — and frogs. Oh so many frogs.

Adee takes us back to the 18th century lab of Luigi Galvani, an Italian scientist hunting for what gives animals the spark of life. His gruesome experiments on twitching frog legs offered proof that animal bodies generate their own electricity, an idea that was hotly debated at the time. (So many scientists repeated Galvani’s experiments, in fact, that Europe began to run out of frogs.)

But around the same time, Galvani critic Alessandro Volta, another Italian scientist, invented the electric battery. It was the kind of razzle-dazzle, history-shaking device that stole the spotlight from animal electricity, and the fledgling field fizzled. “The idea had been set,” Adee writes. “Electricity was not for biology. It was for machines, and telegraphs, and chemical reactions.”
It took decades for scientists to pick up Galvani’s experimental threads and get the study of bioelectricity back on track. Since then, we’ve learned just how much electricity orchestrates our lives, and how much more remains to be discovered. Electricity zips through our neurons, makes our hearts tick and flows in every cell of the body. We’re made up of 40 trillion tiny rechargeable batteries, Adee writes.

She describes how cells use ion channels to usher charged molecules in and out. One thing readers might not expect from a book that illustrates the intricacies of ion channels: It’s surprisingly funny.
Chloride ions, for example, are “perpetually low-key ashamed” because they carry a measly -1 charge. Bogus medical contraptions (here’s looking at you, electric penis belts) were “electro-foolery.” In her acknowledgements, Adee jokes about the “life-saving powers of Voltron” and thanks people for enduring her caffeine jitters. That energy thrums through the book, charging her storytelling like a staticky balloon.

Adee is especially electrifying in a chapter about spinal nerve regeneration and why initial experiments juddered to a halt. Decades ago, scientists tried coaxing severed nerves to link up again by applying an electric field. The controversial technique sparked scientific drama, but the idea of using electricity to heal may have been ahead of its time. Fast-forward to 2020, and DARPA has awarded $16 million to researchers with a similar concept: a bio­electric bandage that speeds wound healing.

Along with zingy Band-Aids of the future, Adee describes other sci-fi–sounding devices in the works. One day, for example, surgeons may sprinkle your brain with neurograins, neural lace or neural dust, tiny electronic implants that could help scientists monitor brain activity or even help people control robotic arms or other devices (SN: 9/3/16, p. 10).

Such implants bring many challenges — like how to marry electronics to living tissue — but Adee’s book leaves readers with a sense of excitement. Not only could bioelectricity inspire new and improved medical devices, it could also reveal a current of unexpected truths about the body.

As Adee writes: “We are electrical machines whose full dimensions we have not even yet dreamed of.”

The April 25 Nepal earthquake killed more than 8,000 people and caused several billion dollars in damage, but new research suggests the toll could have been a lot worse.

GPS readings taken during the quake indicate that most of the tremors vibrated through the ground as long shakes rather than quick pulses. That largely spared the low-lying buildings that make up much of Nepal’s capital, Kathmandu, geophysicists report online August 6 in Science. Those same low-frequency rumbles, though, toppled Kathmandu’s handful of larger buildings, such as the historic 62-meter tall Dharahara Tower.

Understanding why the fault produced a quake at such low frequencies could help seismologists better identify future seismic hazards, says Jean-Philippe Avouac of the University of Cambridge. “This could be some good news not only for this major fault, but also potentially for similar faults around the world.”

Nepal sits over a tectonic boundary where the Indian Plate slips under the Eurasian Plate. At places, the two plates snag together, building stress that abruptly releases as an earthquake (SN: 5/16/15, p. 12).
Earthquakes stronger than April’s magnitude 7.8 shakedown have hit Nepal before, including a magnitude 8.0 quake in 1934. Despite the recent quake’s feebler intensity, its trembles somehow destroyed large buildings that had previously endured mightier earthquakes.

Avouac and colleagues monitored April’s quake using a network of 35 solar-powered GPS stations, the first time such an accurate system was in place during a major quake on this type of fault. The stations measured ground movements five times each second. The earthquake shook most intensely at 0.25 hertz, or one full wave every four seconds, with only moderate shaking above 1 hertz, or one or more complete waves each second.

A building is most vulnerable when shook near its resonance frequency, a range where even small outside forces can result in big vibrations in the structure. Because taller structures have lower resonance frequencies, the April quake’s low-frequency rumbles caused larger buildings to sway and crumble while largely sparing smaller dwellings, the researchers found.

The low frequencies resulted from the smooth and relatively long duration of the tectonic slipping that initiated the quake, the researchers propose. The low-frequency waves then echoed across the region and produced protracted violent shaking.

Determining where future low-frequency quakes will strike could save lives by identifying which building types are most vulnerable to collapse, says geologist Kristin Morell of the University of Victoria in Canada. “These are things that should be built into building codes.”

You’d be forgiven for thinking that depression has a simple explanation.

The same mantra — that the mood disorder comes from a chemical imbalance in the brain — is repeated in doctors’ offices, medical textbooks and pharmaceutical advertisements. Those ads tell us that depression can be eased by tweaking the chemicals that are off-kilter in the brain. The only problem — and it’s a big one — is that this explanation isn’t true.

The phrase “chemical imbalance” is too vague to be true or false; it doesn’t mean much of anything when it comes to the brain and all its complexity. Serotonin, the chemical messenger often tied to depression, is not the one key thing that explains depression. The same goes for other brain chemicals.
The hard truth is that despite decades of sophisticated research, we still don’t understand what depression is. There are no clear descriptions of it, and no obvious signs of it in the brain or blood.

The reasons we’re in this position are as complex as the disease itself. Commonly used measures of depression, created decades ago, neglect some important symptoms and overemphasize others, particularly among certain groups of people. Even if depression could be measured perfectly, the disorder exists amid myriad levels of complexity, from biological confluences of minuscule molecules in the brain all the way out to the influences of the world at large. Countless combinations of genetics, personality, history and life circumstances may all conspire to create the disorder in any one person. No wonder the science is stuck.

It’s easy to see why a simple “chemical imbalance” explanation holds appeal, even if it’s false, says Awais Aftab, a psychiatrist at Case Western Reserve University in Cleveland. What causes depression is nuanced, he says — “not something that can easily be captured in a slogan or buzzword.”

So here, up front, is your fair warning: There will be no satisfying wrap-up at the end of this story. You will not come away with a scientific explanation for depression, because one does not exist. But there is a way forward for depression researchers, Aftab says. It requires grappling with nuances, complexity and imperfect data.

Those hard examinations are under way. “There’s been some really interesting and exciting scientific and philosophical work,” Aftab says. That forward motion, however slow, gives him hope and may ultimately benefit the millions of people around the world weighed down by depression.

How is depression measured?
Many people who feel depressed go into a doctor’s office and get assessed with a checklist. “Yes” to trouble sleeping, “yes” to weight loss and “yes” to a depressed mood would all yield points that get tallied into a cumulative score. A high enough score may get someone a diagnosis. The process seems straightforward. But it’s not. “Even basic issues regarding measurement of depression are actually still quite open for debate,” Aftab says.

That’s why there are dozens of methods to assess depression, including the standard description set by the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders, or DSM-5. This manual is meant to standardize categories of illness.

Variety in measurement is a real problem for the field and points to the lack of understanding of the disease itself, says Eiko Fried, a clinical psychologist at Leiden University in the Netherlands. Current ways of measuring depression “leave you with a really impoverished, tiny look,” Fried says.

Scales can miss important symptoms, leaving people out. “Mental pain,” for instance, was described by patients with depression and their caregivers as an important feature of the illness, researchers reported in 2020 in Lancet Psychiatry. Yet the term doesn’t show up on standard depression measurements.

One reason for the trouble is that the experience of depression is, by its nature, deeply personal, says clinical psychologist Ioana Alina Cristea of the University of Pavia in Italy. Individual patient complaints are often the best tool for diagnosing the disorder, she says. “We can never let these elements of subjectivity go.”

In the middle of the 20th century, depression was diagnosed through subjective conversation and psychoanalysis, and considered by some to be an illness of the soul. In 1960, psychiatrist Max Hamilton attempted to course-correct toward objectivity. Working at the University of Leeds in England, he published a depression scale. Today, that scale, known by its acronyms HAM-D or HRSD, is one of the most widely used depression screening tools, often used in studies measuring depression and evaluating the promise of possible treatments.
“It’s a great scheme for a scale that was made in 1960,” Fried says. Since the HRSD was published, “we have put a man on the moon, invented the internet and created powerful computers small enough to fit in people’s pockets,” Fried and his colleagues wrote in April in Nature Reviews Psychology. Yet this 60-year-old tool remains a gold standard.

Hamilton developed his scale by observing patients who had already been diagnosed with depression. They exhibited symptoms such as weight loss and slowed speech. But those mixtures of symptoms don’t apply to everyone with depression, nor do they capture nuance in symptoms.

To spot these nuances, Fried looked at 52 depression symptoms across seven different scales for depression, including Hamilton’s scale. On average, each symptom appeared in three of the seven scales. A whopping 40 percent of the symptoms appeared in only one scale, Fried reported in 2017 in the Journal of Affective Disorders. The only specific symptom common to all seven scales? “Sad mood.”

In a study that examined depression symptoms reported by 3,703 people, Fried and Randolph Nesse, an evolutionary psychiatrist at the University of Michigan Medical School in Ann Arbor, found 1,030 unique symptom profiles. Roughly 14 percent of participants had combinations of symptoms that were not shared with anyone else, the researchers reported in 2015 in the Journal of Affective Disorders.

Before reliable thermometers, the concept of temperature was murky. How do you understand the science of hot and cold without the tools to measure it? “You don’t,” Fried says. “You make a terrible measurement, and you have a terrible theory of what it is.” Depression presents a similar challenge, he says. Without good measurements, how can you possibly diagnose depression, determine whether symptoms get better with treatments or even prevent it in the first place?

Depression differs by gender, race and culture
The story gets murkier when considering who these depression scales were made for. Symptoms differ among groups of people, making the diagnosis even less relevant for certain groups.
Behavioral researcher Leslie Adams of Johns Hopkins Bloomberg School of Public Health studies depression in Black men. “It’s clear that [depression] is negatively impacting their work lives, social lives and relationships. But they’re not being diagnosed at the same rate” as other groups, she says. For instance, white people have a lifetime risk of major depression disorder of almost 18 percent; Black people’s lifetime risk is 10.4 percent, researchers reported in 2007 in JAMA Psychiatry. This discrepancy led Adams to ask: “Could there be a problem with diagnostic tools?”

Turns out, there is. Black men with depression have several characteristics that common scales miss, such as feelings of internal conflict, not communicating with others and feeling the burdens of societal pressure, Adams and colleagues reported in 2021 in BMC Public Health. A lot of depression measurements are based on questions that don’t capture these symptoms, Adams says. “ ‘Are you very sad?’ ‘Are you crying?’ Some people do not emote in the same way,” she says. “You may be missing things.”

American Indian women living in the Southeast United States also experience symptoms that aren’t adequately caught by the scales, Adams and her team found in a separate study. These women also reported experiences that do not necessarily signal depression for them but generally do for wider populations.

On common scales, “there are some items that really do not capture the experience of depression for these groups,” Adams says. For instance, a common question asks how well someone agrees with the sentence: “I felt everything I did was an effort.” That “can mean a lot of things, and it’s not necessarily tied to depression,” Adams says. The same goes for items such as, “People dislike me.” A person of color faced with racism and marginalization might agree with that, regardless of depression, she says.

Our ways to measure depression capture only a tiny slice of the big picture. The same can be said about our understanding of what’s happening in the brain.

The flawed serotonin hypothesis
Serotonin came into the spotlight in part because of the serendipitous discovery of drugs that affected serotonin receptors, called selective serotonin re­uptake inhibitors, or SSRIs. After getting its start in the late 1960s, the “serotonin hypothesis” flourished in the late ’90s, as advertisers ran commercials that told viewers that SSRIs fixed the serotonin deficit that can accompany depression. These messages changed the way people talked and thought about depression. Having a simple biological explanation helped some people and their doctors, in part by easing the shame some people felt for not being able to snap out of it on their own. It gave doctors ways to talk with people about the mood disorder.

But it was a simplified picture. A recent review of evidence, published in July in Molecular Psychiatry, finds no consistent data supporting the idea that low serotonin causes depression. Some headlines declared that the study was a grand takedown of the serotonin hypothesis. To depression researchers, the findings weren’t a surprise. Many had already realized this simple description wasn’t helpful.

There’s plenty of data suggesting that serotonin, and other chemical messengers such as dopamine and norepinephrine, are somehow involved in depression, including a study by neuropharmacologist Gitte Moos Knudsen of the University of Copenhagen. She and colleagues recently found that 17 people who were in the midst of a depressive episode released, on average, less serotonin in certain brain areas than 20 people who weren’t depressed. The study is small, but it’s one of the first to look at serotonin release in living human brains of people with depression.

But Knudsen cautions that those results, published in October in Biological Psychiatry, don’t mean that depression is fully caused by low serotonin levels. “It’s easy to defer to simple explanations,” she says.

SSRIs essentially form a molecular blockade, stopping serotonin from being reabsorbed into nerve cells and keeping the levels high between the cells. Those high levels are thought to influence nerve cell activity in ways that help people feel better.

Because the drugs can ease symptoms in about half of people with depression, it seemed to make sense that depression was caused by problems with serotonin. But just because a treatment works by doing something doesn’t mean the disease works in the opposite way. That’s backward logic, psychiatrist Nassir Ghaemi of Tufts University School of Medicine in Boston wrote in October in a Psychology Today essay. Aspirin can ease a headache, but a headache isn’t caused by low aspirin.

“We think we have a much more nuanced picture of what depression is today,” Knudsen says. The trouble is figuring out the many details. “We need to be honest with patients, to say that we don’t know everything about this,” she says.

The brain contains seven distinct classes of receptors that sense serotonin. That’s not even accounting for sensors for other messengers such as dopamine and norepinephrine. And these receptors sit on a wide variety of nerve cells, some that send signals when they sense serotonin, some that dampen signals. And serotonin, dopamine and norepinephrine are just a few of dozens of chemicals that carry information throughout a multitude of interconnected brain circuits. This complexity is so great that it renders the phrase “chemical imbalance” meaningless.

Overly simple claims — low serotonin causes depression, or low serotonin isn’t involved — serve only to keep us stymied, Aftab says. “[It] just keeps up that unhelpful binary.”
Depression research can’t ignore the world
In the 1990s, Aftab says, depression researchers got intensely focused on the brain. “They were trying to find the broken part of the brain that causes depression.” That limited view “really hurt depression research,” Aftab says. In the last 10 years or so, “there’s a general recognition that that sort of mind-set is not going to give us the answers.”

Reducing depression to specific problems of biology in the brain didn’t work, Cristea says. “If you were a doctor 10 years ago, the dream was that the neuroscience would give us the markers. We would look at the markers and say, ‘OK. You [get] this drug. You, this kind of therapy.’ But it hasn’t happened.” Part of that, she says, is because depression is an “existentially complicated disorder” that’s tough to simplify, quantify and study in a lab.

Our friendships, our loves, our setbacks and our stress can all influence our health. Take a recent study of first-year doctors in the United States. The more these doctors worked, the higher the rate of depression, scientists reported in October in the New England Journal of Medicine. Similar trends exist for caregivers of people with dementia and health care workers who kept emergency departments open during the COVID-19 pandemic. Their high-stress experiences may have prompted depression in some way.

“Depression is linked to the state of the world — and there is no denying it,” Aftab says.
Today’s research on depression ought to be more pluralistic, Adams says. “There are so many factors at play that we can’t just rest on one solution,” she says. Research from neuroscience and genetics has helped identify brain circuits, chemical messengers, cell types, molecules and genes that all may be involved in the disorder. But researchers aren’t satisfied with that. “There is other evidence that remains unexplored,” Adams says. “With our neuro­science advances, there should be similar advances in public health and psychiatric work.”

That’s happening. For her part, Adams and colleagues have just begun a study looking at moment-to-moment stressors in the lives of Black adolescents, ages 12 to 18, as measured by cell phone questionnaires. Responses, she hopes, will yield clues about depression and risk of suicide.

Other researchers are trying to fit together all of these different ways of seeing the problem. Fried, for example, is developing new concepts of depression that acknowledge the interacting systems. You tug on one aspect of it — using an antidepressant for instance, or changing sleep patterns — and see how the rest of the system reacts.

Approaches like these recognize the complexity of the problem and aim to figure out ways to handle it. We will never have a simple explanation for depression; we are now learning that one cannot possibly exist. That may sound like cold comfort to people in depression’s grip. But seeing the challenge with clear eyes may be the thing that moves us forward.