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Prairie Voles Can Find Partners Just Fine Without The ‘love Hormone’ Oxytocin

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Prairie voles have long been heralded as models of monogamy. Now, a study suggests that the “love hormone” once thought essential for their bonding — oxytocin — might not be so necessary after all.

Interest in the romantic lives of prairie voles (Microtus ochrogaster) was first sparked more than 40 years ago, says Devanand Manoli, a biologist at the University of California, San Francisco. Biologists trying to capture voles to study would frequently catch two at a time, because “what they were finding were these male-female pairs,” he says. Unlike many other rodents with their myriad partners, prairie voles, it turned out, mate for life (SN: 10/5/15).

Pair-bonded prairie voles prefer each other’s company over a stranger’s and like to huddle together both in the wild and the lab. Because other vole species don’t have social behaviors as complex as prairie voles do, they have been a popular animal system for studying how social behavior evolves.

Research over the last few decades has implicated a few hormones in the brain as vital for proper vole manners, most notably oxytocin, which is also important for social behavior in humans and other animals.

Manoli and colleagues thought the oxytocin receptor, the protein that detects and reacts to oxytocin, would be the perfect test target for a new genetic engineering method based on CRISPR technology, which uses molecules from bacteria to selectively turn off genes. The researchers used the technique on vole embryos to create animals born without functioning oxytocin receptors. The team figured that the rodents wouldn’t be able to form pair-bonds — just like voles in past experiments whose oxytocin activity was blocked with drugs.

Instead, Manoli says, the researchers got “a big surprise.” The voles could form pair-bonds even without oxytocin, the team reports in the March 15 Neuron.

“I was very surprised by their results,” says Larry Young, a biologist at Emory University in Atlanta, who was not involved with the study but has studied oxytocin in prairie voles for decades.

A key difference between the new study and past studies that used drugs to block oxytocin is the timing of exactly when the hormone’s activity is turned off. With drugs, the voles are adults and have had exposure to oxytocin in their brains before the shutoff. With CRISPR, “these animals are born never experiencing oxytocin signaling in the brain,” says Young, whose research group has recently replicated Manoli’s experiment and found the same result.

It may be, Young says, that pair-bonding is controlled by a brain circuit that typically becomes dependent on oxytocin through exposure to it during development, like a symphony trained by a conductor. Suddenly remove that conductor and the symphony will sound discordant, whereas a jazz band that’s never practiced with a conductor fares just fine without one.

Manoli agrees that the technique’s timing matters. A secondary reason for the disparity, he says, could be that drugs often have off-target effects, such that the chemicals meant to block oxytocin could have been doing other things in the voles’ brains to affect pair-bonding. But Young disagrees. “I don’t believe that,” he says. “The [drug] that people use is very selective,” not even binding to the receptor of oxytocin’s closest molecular relative, vasopressin. 

Does this result mean that decades of past work on pair-bonding has been upended? Not quite.

“It shows us that this is a much more complicated question,” Manoli says. “The pharmacologic manipulations … suggested that [oxytocin] plays a critical role. The question is, what is that role?”

The new seemingly startling result makes sense if you look at the big picture, Manoli says. The ability for voles to pair-bond is “so critical for the survival of the species,” he says. “From a genetics perspective, it may make sense that there isn’t a single point of failure.”

The group now hopes to look at how other hormones, like vasopressin, influence pair-bonding using this relatively new genetic technique. They are also looking more closely at the voles’ behavior to be sure that the CRISPR gene editing didn’t alter it in a way they haven’t noticed yet.

In the game of vole “love,” it looks like we’re still trying to understand all the players.

Animals

Scientists Have Now Recorded Brain Waves From Freely Moving Octopuses

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For the first time, scientists have recorded brain waves from freely moving octopuses. The data reveal some unexpected patterns, though it’s too early to know how octopus brains control the animals’ behavior, researchers report February 23 in Current Biology.

“Historically, it’s been so hard to do any recordings from octopuses, even if they’re sedated,” says neuroscientist Robyn Crook of San Francisco State University, who was not involved in the study. “Even when their arms are not moving, their whole body is very pliable,” making attaching recording equipment tricky.

Octopuses also tend to be feisty and clever. That means they don’t usually put up with the uncomfortable equipment typically used to record brain waves in animals, says neuroethologist Tamar Gutnick of the University of Naples Federico II in Italy. 

To work around these obstacles, Gutnick and colleagues adapted portable data loggers typically used on birds, and surgically inserted the devices into three octopuses. The researchers also placed recording electrodes inside areas of the octopus brain that deal with learning and memory. The team then recorded the octopuses for 12 hours while the cephalopods went about their daily lives — sleeping, swimming and self-grooming — in tanks.

Some brain wave patterns emerged across all three octopuses in the 12-hour period. For instance, some waves resembled activity in the  human hippocampus, which plays a crucial role in memory consolidation. Other brain waves were similar to those controlling sleep-wake cycles in other animals.

The researchers also recorded some brain waves that they say have never been seen before in any animal. The waves were unusually slow, cycling just two per second, or 2 hertz. They were also unusually strong, suggesting a high level of synchronization between neurons. Sometimes just one electrode picked up the weird waves; other times, they showed up on electrodes placed far apart,

Observing these patterns is exciting, but it’s too early to tell whether they’re tied to a specific behavior or type of cognition, Gutnick says. Experiments with repetitive tasks are necessary to fully understand how these brain areas are activated in octopuses during learning.

The new research is exciting in that it provides a technique for future researchers to observe brain activity in awake and naturally behaving octopuses, Crook says. It could be used to explore brain activity behind the animals’ color-changing abilities, spectacular vision, sleep patterns and adept arm control (SN: 1/29/16; SN: 3/25/21).

Octopuses are highly intelligent, so by studying the creatures “you can get ideas about what is important for intelligence,” Gutnick says. “The problems that the animals face are the same problems, but the solutions that they find are sometimes similar and sometimes different and all of these comparisons teach us something.”

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Static Electricity Helps Parasitic Nematodes Glom Onto Victims

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LAS VEGAS — Some species of parasitic roundworms can catapult themselves high into the air to latch onto fruit flies and other insects. Experiments now reveal that leaping Steinernema carpocapsae nematodes take advantage of a secret weapon that makes them particularly effective in their pursuit of victims: static electricity.

Flying insects build up electric charge as they move through the air (SN: 10/31/22). It’s the same effect that causes electricity to collect on droplets of mist in clouds, and ultimately leads to lightning.

Individual insects can accumulate charges of 100 volts or so, biomechanics researcher Víctor Ortega Jiménez of the University of Maine in Orono reported March 6 at the American Physical Society meeting. When nematodes leap, the charge on a passing insect attracts the parasites like lint to a staticky sweater.

An insect in the top middle of the frame with a rainbow of colors surrounding it. The arrows show the direction the nematodes move; colors indicate relative speed with blue for slower and red for faster. 
As an insect moves, it builds up charges that create surrounding electric fields. Those charges create static electricity that pulls parasitic nematodes toward the insect, new research reveals. The arrows show the direction the nematodes move; colors indicate relative speed with blue for slower and red for faster.Víctor M. Ortega Jiménez

To test the effect of electric charge, Ortega Jiménez and colleagues mounted dead fruit flies on wires and placed them near a surface covered in nematodes. With no charge on a fly, only nematodes that happened to jump in the direction of the insect landed on target, as expected. When researchers applied an electric charge to a suspended fruit fly, even nematodes that initially headed in the wrong direction were caught up in the electric field and pulled onto the fly.

Ortega Jiménez has also studied electric force effects on spider webs. When charged insects neared a web, “the silk is attracted directly to the insects,” he says. That made him wonder whether leaping nematodes rely on those forces as well.

Researchers have long considered the effect of fluids and air flow on insects and other tiny creatures. But only recently have they added electricity to the mix, Ortega Jiménez says. “We need to know how animals actually are dealing with these forces at this scale.”

Some teeny-tiny parasitic roundworms called nematodes have an unerring ability to leap high into the air to land on fruit flies and other living prey. It turns out that the prey unwittingly give the nematodes a hand, new research shows. By simply moving, a fly builds up an electric charge. Like static electric cling, that charge can pull a nematode in. In this experiment, researchers applied an electric charge to a pinned-in-place fly. A speck of a nematode (left) cartwheeled into the air and then headed straight for the fly.

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This Fish Could Expand What We Know About One Odd Deep-Sea Ecosystem

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Off the Pacific coast of Costa Rica sits a deep-sea chimera of an ecosystem. Jacó Scar is a methane seep, where the gas escapes from sediment into the seawater, but the seep isn’t cold like the others found before it. Instead, geochemical activity gives the Scar lukewarm water that enables organisms from both traditionally colder seeps and scalding hot hydrothermal vents to call it home.

One resident of the Scar is a newly identified species of small, purplish fish called an eelpout, described for the first time on January 19 in Zootaxa. This fish is the first vertebrate species found at the Scar and could help scientists understand how the unique ecosystem developed. 

Jacó Scar was discovered during exploration of a known field of methane seeps off the Costa Rican coast and named for the nearby town of Jacó. It is “a really diverse place” with many different organisms living in various microhabitats, says Lisa Levin, a marine ecologist at Scripps Institution of Oceanography in La Jolla, Calif.

Levin was on one of the first expeditions to the Scar but wasn’t involved in the new study. She recalls the team finding and collecting one of the fish during this early excursion, but the researchers didn’t recognize it as a new species.

Several more specimens were snagged during later submersible dives. Charlotte Seid, an invertebrate biologist at Scripps who is working on a checklist of organisms found at the Costa Rican seeps, brought the fishy finds to ichthyologist Ben Frable, also of Scripps, for formal identification.

Frable says he knew the fish was an eelpout. They look exactly as one would expect based on their name: like frowning eels, though they aren’t true eels. But he was having trouble determining what type. Eelpouts are a diverse family of fish comprised of nearly 300 species that can be found all over the world at various ocean depths.

Because the physical differences between species can be subtle, they are “kind of a tricky group” to identify, Frable says. “I just was not really getting anywhere.” So the team turned to eelpout expert Peter Rask Møller of the Natural History Museum of Denmark in Copenhagen, sending him X-rays, pictures and eventually one of the fish specimens.

Møller narrowed the enigmatic eelpout to the genus Pyrolycus, meaning “fire wolf.” Turns out, the tool, called a dichotomous key, that Frable had been using to identify the specimens was outdated, made before Pyrolycus was described in 2002. “I did not know that genus existed,” Frable says.

Because the other two known Pyrolycus species live far away in the western Pacific and have different physical features, the team dubbed the mystery fish P. jaco — a new species.

The first eelpouts most likely evolved in cold waters, Frable says, but many have since made their home in the scalding waters of hydrothermal vents. Of the 24 known fish species that live only at hydrothermal vents, “13 of them are eelpouts,” Frable says.

A Pyrolycus jaco specimen is shown freshly collected (top), preserved (middle) and in X-rays superimposed over the fresh image (bottom), all on a black background.
A Pyrolycus jaco specimen is shown freshly collected (top), preserved (middle) and in X-rays superimposed over the fresh image (bottom).B. Frable and C. Seid/Scripps Institution of Oceanography

The new finding raises questions about how the known Pyrolycus species came to live so far apart. It may have to do with the fact that methane seeps are more common than previously thought on the ocean floor, and if some are lukewarm like Jacó Scar, the new species could have used them as refuges while moving east.

And by comparing P. jaco to its vent-living relatives, researchers may be able to figure out how it adapted to live in the tepid waters of the Scar — which may provide clues to how other species living there did too.

The eelpout is part of a medley of other species that form Jacó Scar’s composite ecosystem, along with, for example, clams typically found at cold seeps and bacteria found at hydrothermal vents. Jacó Scar is a “mixing bowl” of species found in other parts of the world, Seid says. Figuring out how this eclectic bunch interacts “is part of the fun.”

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