In the shallows off Fiji’s Pacific shores, two marine researchers from the Georgia Institute of Technology for a new study assembled groups of corals that were all of the same species, i.e. groups without species diversity. When Cody Clements snorkeled down for the first time to check on them, his eyes instantly told him what his data would later reveal.

“One of the species had entire plots that got wiped out, and they were overgrown with algae,” Clements said. “Rows of corals had tissue that was brown — that was dead tissue. Other tissue had turned white and was in the process of dying.”

36 ghastly plots

Clements, a postdoctoral researcher and the study’s first author, also assembled groups of corals with a mixture of species, i.e. biodiverse groups, for comparison. In total, there were 36 single-species plots, or monocultures. Twelve additional plots contained polycultures that mixed three species.

By the end of the 16-month experiment, monocultures had faired obviously worse. And the study had shown via the measurably healthier growth in polycultures that science can begin to quantify biodiversity’s contribution to coral survival as well as the effects of biodiversity’s disappearance.

“This was a starter experiment to see if we would get an initial result, and we did,” said principal investigator Mary Hay, a Regents Professor and Harry and Linda Teasley Chair in Georgia Tech’s School of Biological Sciences. “So much reef death over the years has reduced coral species variety and made reefs more homogenous, but science still doesn’t understand enough about how coral biodiversity helps reefs survive. We want to know more.”

The results of the study appear in the February issue of the journal Nature Ecology and Evolution and were made available online on January 7, 2018. The research was funded by the National Science Foundation, by the National Institutes of Health’s Fogarty International Center, and by the Teasley Endowment.

The study’s insights could aid ecologists restocking crumbling reefs with corals — which are animals. Past replenishing efforts have often deployed patches of single species that have had trouble taking hold, and the researchers believe the study should encourage replanting using biodiverse patches.

40 years’ decimation

The decimation of corals Hay has witnessed in over four decades of undersea research underscores this study’s importance.

“It’s shocking how quickly the Caribbean reefs crashed. In the 1970s and early 1980s, reefs consisted of about 60 percent live coral cover,” Hay said. “Coral cover declined dramatically through the 1990s and has remained low. It’s now at about 10 percent throughout the Caribbean.”

“You used to find living diverse reefs with structurally complex coral stands the size of city blocks. Now, most Caribbean reefs look more like parking lots with a few sparse corals scattered around.”

84 percent loss

The fact that the decimation in the Pacific is less grim is bitter irony. About half of living coral cover disappeared there between the early 1980s and early 2000s with declines accelerating since.

“From 1992 to 2010, the Great Barrier Reef, which is arguably the best-managed reef system on Earth, lost 84 percent,” Clements said. “All of this doesn’t include the latest bleaching events reported so widely in the media, and they killed huge swaths of reef in the Pacific.”

The 2016 bleaching event also sacked reefs off of Fiji where the researchers ran their experiment. The coral deaths have been associated with extended periods of ocean heating, which have become much more common in recent decades.

10 times more species

Still, there’s hope. Pacific reefs support ten times as many coral species as Caribbean reefs, and Clements’ and Hay’s new study suggests that this higher biodiversity may help make these reefs more robust than the Caribbean reefs. There, many species have joined the endangered list, or are “functionally extinct,” still present but in traces too small to have ecological impact.

The Caribbean’s coral collapse may have been a warning shot on the dangers of species loss. Some coral species protect others from getting eaten or infected, for example.

“A handful of species may be critical for the survival of many others, and we don’t yet know well enough which are most critical. If key species disappear, the consequences could be enormous,” said Hay, who believes he may have already witnessed this in the Caribbean. “The decline of key species may drive the decline of others and potentially create a death spiral.”

864 abrasive animals

Off Fiji’s shores, Clements transported by kayak, one by one, 48 concrete tables he had built on land. He dove them into place and mounted on top of them 864 jaggy corals in planters he had fashioned from the tops of plastic soda bottles.

“I scratched a lot of skin off of my fingers screwing those corals onto the tables,” he said, laughing at the memory. “I drank enough saltwater through my snorkel doing it, too.”

Clements laid out 18 corals on each tabletop: Three groups of monocultures filled 36 tables (12 with species A, 12 with species B, 12 with species C). The remaining 12 tabletops held polycultures with balanced A-B-C mixtures. He collected data four months into the experiment and at 16 months.

The polycultures all looked great. Only one monoculture species, Acropora millepora, had nice growth at the 16-month mark, but that species is more susceptible to disease, bleaching, predators, and storms. It may have sprinted ahead in growth in the experiment, but long-term it would probably need the help of other species to cope with its own fragility.

“Corals and humans both may do well on their own in good times,” Hay said. “But when disaster strikes, friends may become essential.”

Skyrmions are nanoscale whirls or vortices of magnetic poles that form lattices within a magnetic material, a type of quasiparticle that can zip across the material, pushed by electrical current. Those properties have captured the fascination of scientists, who think the phenomenon could lead to the next big advance in data storage, making digital technology even faster and smaller.

There are some big challenges to overcome, however. Until recently skyrmions were a phenomenon only observed at extreme low temperature. Also, external magnetic forces makes them currently impractical for applications.

“In order to be really useful in a device, these magnetic vortices need to be able to exist without the ‘help’ of an external magnetic field,” said Lin Zhou, a scientist in the Ames Laboratory’s Division of Materials Sciences and Engineering.

With that in mind, she and other researchers at Ames Laboratory investigated FeGe, an iron-germanium magnetic material that has demonstrated skyrmions in the highest temperature ranges to date in crystals with a similar, or B20 structure.

Ames Lab scientists with external collaborators were able to establish a skyrmion lattice in a sample through exposure to magnetic fields and supercooling with liquid nitrogen. With a high resolution microscopy method called Lorentz transmission electron microscopy (L-TEM), the team was able to observe the skyrmion lattice in zero magnetic field, and then observe the decay of the skyrmions as the temperature warmed. This direct observation yielded critical new information about how skyrmions behave and how they revert back to a ‘normal’ (what scientists call metastable) magnetic state.

“We’ve stabilized these skyrmions without a magnetic field, and our microscopy techniques allowed us to really see how the vortices change over time, temperature, and magnetic field; we think it provides a very solid foundation for theorists to better understand this phenomenon,” Zhou said.

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Materials provided by DOE/Ames Laboratory. Note: Content may be edited for style and length.

The findings from scientists at the USC Michelson Center for Convergent Bioscience and Nagoya University’s Institute of Transformative BioMolecules (ITbM) advance a burgeoning area of research: turning the body’s circadian rhythms against cancer.

Their study, conducted on human kidney cancer cells and on acute myeloid leukemia in mice, was published Jan. 23 in the journal Science Advances.

Scientists know that disrupting sleep and other elements of humans’ circadian rhythm can harm health. The same is true for the circadian clock of cells themselves. If researchers could disturb the circadian clock of cancer cells, they theorize, they could potentially hurt or kill those cells.

The scientists found that a molecule named GO289 targets an enzyme that controls the cell’s circadian rhythm. This drug-protein interaction then disrupts the functions of four other proteins that are important for cell growth and survival.

In effect, GO289 can jam the cogs of the cell’s circadian clock, slowing its cycles. And it can do so with little impact to healthy cells.

“In some cancers, the disease takes over the circadian clock mechanism and uses it for the evil purpose of helping itself grow,” said Steve Kay, director of convergent biosciences at the USC Michelson Center and USC Provost Professor of Neurology, Biomedical Engineering and Biological Sciences. “With GO289, we can interfere with those processes and stop the cancer from growing.”

Kay is among several scientists from USC Dornsife College of Letters, Arts and Sciences, USC Viterbi School of Engineering and Keck School of Medicine at USC who are collaborating across multiple disciplines to find new solutions for treating cancer, neurological disease and cardiovascular disease.

Finding the right candidate

On its initial interactions with human bone cancer cells, GO289 appeared to slow the tumors’ circadian clock as it targeted an enzyme, named CK2.

To see if GO289 consistently hindered other cancers in the same way, the scientists then tested it on human kidney cancer cells and on mice with acute myeloid leukemia. They found that GO289 specifically affected cancer cell metabolism and other circadian-related functions that normally would enable the cancer to grow and spread.

Kay is optimistic about the findings. “This could become an effective new weapon that kills cancer,” he said.

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Materials provided by University of Southern California. Original written by Emily Gersema. Note: Content may be edited for style and length.