Modern birds evolved from dinosaurs, but it’s not clear how well birds’ ancient dino ancestors could fly (SN: 10/28/16). Now, a look at the fossilized feet of one nonavian dinosaur suggests that it may have hunted on the wing, like some hawks today.

The crow-sized Microraptor had toe pads very similar to those of modern raptors that can hunt in the air, researchers report December 20 in Nature Communications. That means the feathered, four-winged dinosaur probably used its feet to catch flying prey too, paleobiologist Michael Pittman of the Chinese University of Hong Kong and colleagues say (SN: 7/16/20).
Other researchers caution that toe pads alone aren’t enough to declare Microraptor an aerial hunter. But if the claim holds up, such a hunting style would reinforce a debated hypothesis that powered flight evolved multiple times among dinosaurs, a feat once attributed solely to birds.

Toe pads are bundles of scale-covered flesh on the undersides of dinosaur feet, similar to “toe beans” on dogs and cats. Because the pads are points where the living animal interacted with surfaces, toe pads give paleontologists a “sense of where the rubber meets the road,” says Alexander Dececchi, a paleontologist at Mount Marty University in Yankton, S.D., who was not involved in the new study.

These contact points can paint a clearer picture of an animal’s behavior by providing “details that the skeleton itself wouldn’t show,” says Thomas Holtz Jr., a dinosaur paleobiologist at the University of Maryland in College Park, who was also not involved in the study.

To investigate dinosaur toe pads, Pittman and colleagues turned to the Shandong Tianyu Museum of Nature in Linyi, China. It “has arguably the largest collection of feathered dinosaurs in the world, and, importantly, they haven’t been prepared extensively,” Pittman says. Many of these dinosaur skeletons are still surrounded by rock, which is where soft tissues can be preserved. Such a specimen “gives us the best chance of finding this wonderful soft tissue information,” he says.
Using special lasers that cause the otherwise nearly invisible soft tissue in the fossils to fluoresce, the team found 12 specimens with exceptionally well-preserved toe pads among the thousands examined (SN: 3/20/17).

The team compared the fossil toe pads with those of 36 types of modern birds, whose toe pads vary with their lifestyle. Predatory birds, for example, have protruding toe pads with spiky scales for grasping prey, while ground birds that spend their time walking and running have flatter toe pads. The analysis showed that Microraptor’s toe pads and other aspects of the feet, like the shape of the toe joints and claws, are most like those of modern hawks. That similarity suggests that the dinosaur could hunt prey midair and on the ground like hawks do, the team says.

Other dinosaurs, like the feathered Anchiornis, had flatter toe pads and straighter claws, suggesting a terrestrial lifestyle. That’s in line with ideas about this dinosaur being a poor flier, Pittman says.
The idea that Microraptor hunted like a hawk is consistent with other fossil evidence. One Microraptor fossil has been found with a bird in its stomach, and Microraptor‘s skeletal and soft tissue anatomy suggest some powered flight capability.

There’s still more work to do to figure out how well the dinosaur may have flown. “Microraptor is not a bird, but a close relative. Just because it has feet like a predatory bird doesn’t necessarily mean it must be catching prey in the exact same way,” Pittman says. But Microraptor’s hawklike lifestyle “is a strong possibility,” he adds.
Flight could have been useful to Microraptor when hunting, even if it couldn’t stack up to today’s fliers. Dececchi speculates that Microraptor’s anatomy probably prevented it from outflying birds, but may have helped it surprise otherwise out-of-reach prey, including flying and gliding animals.

“You only have to be fast or aerobatic enough to catch other things in your environment,” Holtz says. “So, it’s not improbable that [Microraptor was] catching things in the air on occasion.”

Other paleontologists are more skeptical that Microraptor hunted on the wing. “It would be a bit of a stretch to me to suggest that Microraptor was pursuing prey in an aerial context,” says Albert Chen, a paleobiologist at the University of Cambridge. The new findings inform only “what the foot was used for.”

Alternative hypotheses, such as a completely or partially terrestrial hunting style, could fit the data too, Holtz says, but the “feet are definitely playing a major role in their prey capture,” whether on the ground or in the air.

For now, the picture of Microraptor’s ecology remains fuzzy, but as lasers continue to increase the picture’s resolution, our understanding of dinosaur flight may reach new heights.

The sperm whale is an endangered species. A major reason is that the whale oil is heat-resistant and chemically and physically stable. This makes it useful for lubricating delicate machinery. The only substitute is expensive carnauba wax from the leaves of palm trees that grow only in Brazil … [but] wax from the seeds of the jojoba, an evergreen desert shrub, is nearly as good.

Update
After sperm whale oil was banned in the early 1970s, the United States sought to replenish its reserves with eco-friendly oil from jojoba seeds (SN: 5/17/75, p. 335). Jojoba oil’s chemical structure is nearly identical to that of sperm whale oil, and the shrub is native to some North American desert ecosystems, making the plant an appealing replacement. Today, jojoba shrubs are cultivated around the world on almost every continent. Jojoba oil is used in hundreds of products, including cosmetics, pharmaceuticals, adhesives and lubricants. Meanwhile, sperm whale populations have started to recover under international anti-whaling agreements (SN: 2/27/21, p. 4).

Higher and higher still, the cotton bollworm moth caterpillar climbs, its tiny body ceaselessly scaling leaf after leaf. Reaching the top of a plant, it will die, facilitating the spread of the virus that steered the insect there.

One virus behind this deadly ascent manipulates genes associated with caterpillars’ vision. As a result, the insects are more attracted to sunlight than usual, researchers report online March 8 in Molecular Ecology.

The virus involved in this caterpillar takeover is a type of baculovirus. These viruses may have been evolving with their insect hosts for 200 million to 300 million years, says Xiaoxia Liu, an entomologist at China Agricultural University in Beijing. Baculoviruses can infect more than 800 insect species, mostly the caterpillars of moths and butterflies. Once infected, the hosts exhibit “tree-top disease,” compelled to climb before dying and leaving their elevated, infected cadavers for scavengers to feast upon.
The clever trick of these viruses has been known for more than a century, Liu says. But how they turn caterpillars into zombies doomed to ascend to their own deaths wasn’t understood.

Previous research suggested that infected caterpillars exhibit greater “phototaxis,” meaning they are more attracted to light than uninfected insects. Liu and her team confirmed this effect in the laboratory using cotton bollworm moth caterpillars (Helicoverpa armigera) infected with a baculovirus called HearNPV.

The researchers compared infected and uninfected caterpillars’ positions in glass tubes surrounding a climbing mesh under an LED light. Uninfected caterpillars would wander up and down the mesh, but would return to the bottom before pupating. That behavior makes sense because in the wild, this species develops into adults underground. But infected hosts would end up dead at the top of the mesh. The higher the source of light, the higher infected hosts climbed.

The team moved to the horizontal plane to confirm that the hosts were responding to light rather than gravity, placing caterpillars in a hexagonal box with one of the side panels illuminated. By the second day after infection, host caterpillars crawled to the light about four times as often as the uninfected.

When the researchers surgically removed infected caterpillars’ eyes and put the insects in the box, the blinded insects were attracted to the light a quarter as often as unaltered infected hosts. That suggested that the virus was using a caterpillar’s vision against itself.

The team then compared how active certain genes were in various caterpillar body parts in infected and uninfected larvae. Detected mostly in the eyes, two genes for opsins, the light-sensitive proteins that are fundamental for vision, were more active after an infection with the virus, and so was another gene associated with vision called TRPL. It encodes for a channel in cell membranes involved in the conversion of light into electrical signals.

When the team used the gene-editing tool CRISPR/Cas9 to shut off the opsin genes and TRPL in infected caterpillars, the number of hosts attracted to the light in the box was cut roughly in half. Their height at death on the mesh was also reduced.

Baculoviruses appear capable of commandeering the genetic architecture of caterpillar vision, exploiting an ancient importance of light for insects, Liu says.

Light can cue crucial biological processes in insects, from directing their developmental timing, to setting their migration routes.

These viruses were already known to be master manipulators in other ways, tweaking their hosts’ sense of smell, molting patterns and the programmed death of cells, says Lorena Passarelli, a virologist at Kansas State University in Manhattan, who was not involved with the study. The new research shows that the viruses manipulate “yet another physiological host process: visual perception.”

There’s still a lot to learn about this visual hijacking, Passarelli says. It’s unknown, for instance, which of the virus’s genes are responsible for turning caterpillars into sunlight-chasing zombies in the first place.

Some bacteria carry tiny syringes filled with chemicals that may thin out competitors or incapacitate predators. Now, researchers have gotten up-close views of these syringes, technically known as contractile injection systems, from a type of cyanobacteria and a marine bacterium.

Figuring out how key parts of the molecular syringes work may help scientists devise their own nanomachines. Artificial injection machines could direct antibiotics against troublesome bacteria while leaving friendly microbes untouched.

Genes encoding pieces of the injection machinery are found in many bacterial species. But, “just by looking at the genes, it’s quite hard to predict how these contractile injection systems work,” says Gregor Weiss, a cellular structural biologist at ETH Zurich.
So Weiss and colleagues examined bacterial syringes using cryo-electron microscopy, in which cells are flash frozen to capture cellular structures as they typically look in nature (SN: 6/22/17).

Previously, researchers have found syringes anchored in some bacteria’s outer membranes, where the bacteria can shoot their payload into cells they bump into. Other species’ injectors squirt their contents into the environment.

But in a type of cyanobacteria called Anabaena, the syringes are in an unusual place, nestled in the membrane of the internal structure where the bacteria carry out photosynthesis, Weiss and colleagues report in the March Nature Microbiology. Buried inside the cells, “it’s hard to imagine how [the syringes] could get out and interact with the target organism,” Weiss says.
Anabaena may use its syringes against itself to trigger programmed cell death when the cyanobacteria come under stress. In the team’s experiments, ultraviolet light or high salt levels in water triggered some syringes to dump their payload. That led to the death of some Anabaena cells in the long chains that the cyanobacteria grow in, forming hollow “ghost cells.”

Ghost cells shed their outer wall and membrane, exposing unfired syringes in the inner membrane to the outside. The ghosts may act like Trojan horses, delivering their deadly payload to predators or competitors, the team hypothesizes. The researchers haven’t yet found which organisms are the probable targets of Anabaena’s syringes.

Inside a type of marine bacteria called Algoriphagus machipongonensis, the story is a bit different. Here, the syringes have a different architecture and float unmoored within the bacterial cell, ETH Zurich’s Charles Ericson and colleagues report in the March Nature Microbiology. The injectors are also found in the liquid in which the bacteria are grown in the laboratory, but how they get out of the cell is a mystery. Perhaps they are released when the bacteria die or get eaten by a predator, Ericson says.

The team also found two proteins loaded inside the Algoriphagus’ syringes, but what those proteins do isn’t known. The researchers tried genetically engineering E. coli to produce one of the proteins, but it kills the bacteria, says study coauthor Jingwei Xu, also at ETH Zurich.
Comparing the structures of syringes from various species, the researchers identified certain structures within the machines that are similar, but slightly different from species to species. Learning how those modifications change the way the injectors work may allow researchers to load different cargoes into the tubes or target the syringes against specific bacteria or other organisms. “Now we have the general blueprint,” Ericson says, “can we re-engineer it?”