Category: 7. Science

  • The sugar that sparked life: Why ribose was RNA’s first choice

    The sugar that sparked life: Why ribose was RNA’s first choice

    In living organisms today, complex molecules like RNA and DNA are constructed with the help of enzymes. So how did these molecules form before life (and enzymes) existed? Why did some molecules end up as the building blocks of life and not others? A new study by Scripps Research scientists helps answer these longstanding questions.

    The results, published in the chemistry journal Angewandte Chemie on June 27, 2025, showhow ribose may have become the sugar of choice for RNA development. They found that ribose binds to phosphate — another molecular component of RNA — more quickly and effectively than other sugar molecules. This feature could have helped select ribose for inclusion in the molecules of life.

    “This gives credence to the idea that this type of prebiotic chemistry could have produced the building blocks of RNA, which then could have led to entities which exhibit lifelike properties,” says corresponding author Ramanarayanan Krishnamurthy, professor of chemistry at Scripps Research.

    Nucleotides, the building blocks of RNA and DNA, consist of a five-carbon sugar molecule (ribose or deoxyribose) that is bound to a phosphate group and a nitrogen-based base (the part of the molecule that encodes information, e.g., A, C, G or U). Krishnamurthy’s research aims to understand how these complex molecules could have arisen on primordial Earth. Specifically, this study focused on phosphorylation, the step within nucleotide-building where ribose connects to the phosphate group.

    “Phosphorylation is one of the basic chemistries of life; it’s essential for structure, function and metabolism,” says Krishnamurthy. “We wanted to know, could phosphorylation also play a fundamental role in the primordial process that got all of these things started?”

    From previous work, the team knew that ribose could become phosphorylated when combined with a phosphate-donating molecule called diamidophosphate (DAP). In this study, they wanted to know whether other, similar sugars could also undergo this reaction, or whether there is something special about ribose.

    To test this, the researchers used controlled chemical reactions to investigate how quickly and effectively ribose is phosphorylated by DAP compared to three other sugar molecules with the same chemical makeup but a different shape (arabinose, lyxose and xylose). Then, they used an analytical technique called nuclear magnetic resonance (NMR) spectroscopy to characterize the molecules produced by each reaction.

    They showed that although DAP was able to phosphorylate all four sugars, it phosphorylated ribose at a much faster rate. Additionally, the reaction with ribose resulted exclusively in ring-shaped structures with five corners (e.g., 5-member rings), whereas the other sugars formed a combination of 5- and 6-member rings.

    “This really showed us that there is a difference between ribose and the three other sugars,” says Krishnamurthy. “Ribose not only reacts faster than the other sugars, it’s also more selective for the five-member ring form, which happens to be the form that we see in RNA and DNA today.”

    When they added DAP to a solution containing equal amounts of the four different sugars, it preferentially phosphorylated ribose. And whereas the other three sugars got “stuck” at an intermediate point in the reaction, a large proportion of the ribose molecules were converted into a form that could likely react with a nuclear base to form a nucleotide.

    “What we got was a 2-in-1: We showed that ribose is selectively phosphorylated from a mixture of sugars, and we also showed that this selective process produces a molecule with a form that is conducive for making RNA,” says Krishnamurthy. “That was a bonus. We did not anticipate that the reaction would pause at the stage advantageous for producing nucleotides.”

    The researchers caution that, even if these reactions can all occur abiotically, it doesn’t mean that they are the reactions that necessarily resulted in life.

    “Studying these types of chemistries helps us understand what sort of processes might have led to the molecules that constitute life today, but we are not making the claim that this selection is what led to RNA and DNA, because that’s quite a leap,” says Krishnamurthy. “There are a lot of other things that need to happen before you get to RNA, but this is a good start.”

    In future research, the team plans to test whether this chemical reaction can occur inside primitive cellular structures called “protocells.”

    “The next question is, can ribose be selectively enriched within a protocell, and can it further react to make nucleotides within a protocell?” says Krishnamurthy. “If we can make that happen, it might produce enough tension to force the protocell to grow and divide — which is exactly what underpins how we grow.”

    In addition to Krishnamurthy, the study “Selection of Ribofuranose-Isomer Among Pentoses by Phosphorylation with Diamidophosphate” was co-authored by Harold A. Cruz of Scripps Research.

    The work was supported by the NASA Astrobiology Exobiology grant (80NSSC22K0509).

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  • Moon phase today explained: What the moon will look like on July 23, 2025

    Moon phase today explained: What the moon will look like on July 23, 2025

    Looking up at the sky and wondering where the moon is? Today’s lack of beautiful moonlight isn’t a mystery; it’s to do with where we are in the lunar cycle. What’s that, you ask? Keep reading to find out.

    The lunar cycle is a series of eight unique phases of the moon’s visibility. The whole cycle takes about 29.5 days, according to NASA, and these different phases happen as the Sun lights up different parts of the moon whilst it orbits Earth. 

    So, what’s happening tonight, July 23, and where are we in the lunar cycle? Keep reading to find out.

    What is today’s moon phase?

    As of Wednesday, July 23, the moon phase is Waning Crescent, and it is almost completely hidden to us on Earth. The moon will only be 2% visible to us tonight, according to NASA’s Daily Moon Observation.

    On day 28 of the lunar cycle, there’s unfortunately nothing visible on the moon due to how little of it is illuminated.

    When is the next full moon?

    The next full moon will be on August 9. The last full moon was on July 10.

    What are moon phases?

    According to NASA, moon phases are caused by the 29.5-day cycle of the moon’s orbit, which changes the angles between the Sun, Moon, and Earth. Moon phases are how the moon looks from Earth as it goes around us. We always see the same side of the moon, but how much of it is lit up by the Sun changes depending on where it is in its orbit. This is how we get full moons, half moons, and moons that appear completely invisible. There are eight main moon phases, and they follow a repeating cycle:

    Mashable Light Speed

    New Moon – The moon is between Earth and the sun, so the side we see is dark (in other words, it’s invisible to the eye).

    Waxing Crescent – A small sliver of light appears on the right side (Northern Hemisphere).

    First Quarter – Half of the moon is lit on the right side. It looks like a half-moon.

    Waxing Gibbous – More than half is lit up, but it’s not quite full yet.

    Full Moon – The whole face of the moon is illuminated and fully visible.

    Waning Gibbous – The moon starts losing light on the right side.

    Last Quarter (or Third Quarter) – Another half-moon, but now the left side is lit.

    Waning Crescent – A thin sliver of light remains on the left side before going dark again.

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  • Study reveals how the body clock stays on track despite temperature changes

    Study reveals how the body clock stays on track despite temperature changes

    Researchers led by Gen Kurosawa at the RIKEN Center for Interdisciplinary Theoretical and Mathematical Sciences (iTHEMS) in Japan have used theoretical physics to discover how our biological clock maintains a consistent 24-hour cycle-even as temperatures change. They found that this stability is achieved through a subtle shift in the “shape” of gene activity rhythms at higher temperatures, a process known as waveform distortion. This process not only helps keep time steady but also influences how well our internal clock synchronizes with the day-night cycle. The study was published in PLOS Computational Biology on July 22.

    Have you ever wondered how your body knows when it’s time to sleep or wake up? The simple answer is that your body has a biological clock, which runs on a roughly 24-hour cycle. But because most chemical reactions speed up as temperatures rise, how our bodies compensate for changing temperatures throughout the year-or even as we move back and forth between the outdoor summer heat and indoor air-conditioned rooms-has remained largely a mystery.

    Our biological clock is powered by cyclical patterns of mRNA-the molecules that code for protein production-which result from certain genes being rhythmically turned on and off. Just as the back and forth of a swinging pendulum over time can be described mathematically as a sine wave, smoothly going up and coming down over and over, so can the rhythm of mRNA production and decline.

    Kurosawa’s research team at RIKEN iTHEMS and a collaborator at YITP, Kyoto University, drew on theoretical physics to analyze the mathematical models that describe this rhythmic rise and fall of mRNA levels. Specifically, they used the renormalization group method, a powerful approach adapted from physics, to extract critical slow-changing dynamics from the system of mRNA rhythms. Their analysis revealed that at higher temperatures mRNA levels should rise more quickly and decline more slowly, but importantly, the duration of one cycle should stay constant. When graphed, this high-temperature rhythm looks like a skewed, asymmetrical waveform.

    But does this theorized change actually happen? To test this theory in real organisms, the researchers examined experimental data from fruit flies and mice. Sure enough, at higher temperatures, these animals showed the predicted waveform distortions, confirming that the theoretical predictions align with biological reality. The researchers conclude that waveform distortion is the key to temperature compensation in the biological clock, specifically the slowing down of mRNA-level decline during each cycle.

    The team also found that waveform distortion affects how well the biological clock synchronizes with environmental cues, such as light and darkness. The analysis predicted that when the waveform becomes more distorted, the biological clock is more stable, and environmental cues have little effect on it. This theoretical prediction matches experimental observations in flies and fungi and is significant because irregular light-dark cycles are part of modern-day life for most people.

    Our findings show that waveform distortion is a crucial part of how biological clocks remain accurate and synchronized, even when temperatures change.”


    Gen Kurosawa, RIKEN Center for Interdisciplinary Theoretical and Mathematical Sciences

    He adds that future research can now focus on identifying the exact molecular mechanisms that slow down the decline in mRNA levels, which leads to the waveform distortion. Scientists also hope to explore how this distortion varies across species-or even between individuals-since age and personal differences may influence how our internal clocks behave.

    “In the long term,” Kurosawa notes, “the degree of waveform distortion in clock genes could be a biomarker that helps us better understand sleep disorders, jet lag, and the effects of aging on our internal clocks. It might also reveal universal patterns in how rhythms work-not just in biology, but in many systems that involve repeating cycles.”

    Source:

    Journal reference:

    Gibo, S., et al. (2025). Waveform distortion for temperature compensation and synchronization in circadian rhythms: An approach based on the renormalization group method. PLOS Computational Biology. doi.org/10.1371/journal.pcbi.1013246.

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  • Super-resolution X-ray technique uncovers atomic structures

    Super-resolution X-ray technique uncovers atomic structures

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  • These DNA Structures Could Rewrite the Rules of Light, Sound, and Matter – SciTechDaily

    1. These DNA Structures Could Rewrite the Rules of Light, Sound, and Matter  SciTechDaily
    2. DNA moiré superlattices  Nature
    3. Scientists twist DNA into self-building nanostructures that could transform technology  ScienceDaily
    4. Programmable DNA moiré superlattices: Expanding the material design space at the nanoscale  Phys.org

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  • New insights reveal how FtsZ and ZapA cooperate during bacterial cell division

    New insights reveal how FtsZ and ZapA cooperate during bacterial cell division

    Bacterial cell division, a process wherein a single cell divides to form two identical daughter cells, represents one of the most essential biological processes. Understanding the precise mechanism behind this dynamic process can help in the development of targeted ways to inhibit bacterial proliferation.

    The process of cell division involves multiple proteins and their complex interactions. FtsZ protein molecules polymerize to form protofibrils that further associate into a ring-like structure called the Z-ring. Z-ring formation is a crucial step in the cell division process, facilitated by multiple FtsZ-associated proteins. ZapA is one such protein, which is conserved widely among multiple bacterial species and is expressed in significantly high levels. The ZapA protein binds to FtsZ protofilaments, assisting in the formation and maintenance of the Z-ring. However, multiple aspects of bacterial cell division remain unexplored, including the exact structure of the FtsZ-ZapA protein complex and the underlying mechanism of interaction.

    While previous studies have characterized these proteins separately, researchers wanted to understand their dynamic interaction. Professor Hiroyoshi Matsumura from the College of Life Sciences, Ritsumeikan University, Japan, had led a previous study published in Nature Communications in 2023, titled ‘Structures of a FtsZ single protofilament and a double-helical tube in complex with a monobody,’ which focused on the structure of FtsZ protofilaments. Building on that work, the researchers sought to understand the dynamic interaction between the FtsZ and ZapA proteins.

    Now, in a new study led by Prof. Matsumura, published in Nature Communications on July 1, 2025, the researchers have finally been able to gain insights into the cooperative functioning of these two proteins. Dr. Ryo Uehara from Ritsumeikan University, Dr. Takayuki Uchihashi from Nagoya University and ExcCELLs, Dr. Keiichi Namba, Dr. Junso Fujita, and Dr. Kazuki Kasai, all from the University of Osaka, were also involved in this study. “FtsZ is a potential therapeutic target for bacterial infections. Hence, we wanted to understand how it maintains its dynamic nature while interacting with ZapA protein and the overall structure of the complex,” says Prof. Matsumura while explaining the main inspiration behind their research.

    For the study, FtsZ and ZapA proteins from the bacteria Klebsiella pneumoniae were analyzed. The scientists utilized cryo-electron microscopy, a high-resolution microscopy technique, to visualize the three-dimensional structure of FtsZ and ZapA. Next, they used high-speed atomic force microscopy to understand the cooperative interaction between the two proteins.

    Their analysis revealed that four units of ZapA protein molecules form the ZapA tetramer, which tethers to FtsZ protofilaments to form an asymmetric ladder-like structure. In this ladder-like arrangement, a single FtsZ filament is precisely held between two parallel FtsZ filaments on one side. On the other side, it is tethered to a double anti-parallel protofilament. “In an anti-parallel protofilament, the filaments run alongside each other, but the subunits are aligned in opposite directions,” explains Prof. Matsumura. Thus, ZapA impacts the alignment of the FtsZ filament, which further influences the formation of the Z-ring structure. Furthermore, ZapA and FtsZ were observed to interact extensively over large surface areas, and this contact caused minor structural alterations in FtsZ conformation.

    Notably, the team also revealed the existence of electrostatic repulsion within the anti-parallel double filament. This repulsive force is thought to enhance the mobility of FtsZ filaments, enabling them to maintain their dynamic nature without any interference.

    The team also captured the real-time dynamics of ZapA-FtsZ interaction. The interaction was found to be dynamic in nature, with repeated binding and dissociation, which helps to maintain the mobility of the filaments. They described the interaction as cooperative binding. Once ZapA binds to FtsZ, some structural change is observed. This makes the adjacent FtsZ molecule more accessible for the next ZapA molecule,” said Prof. Matsumura while explaining the cooperative interaction.

    This study has revealed the intricate mechanism of bacterial cell division, paving the way for the development of new antibacterial agents. The study also highlights the synergy between cryo-electron microscopy and high-speed atomic force microscopy, demonstrating how combining these tools can unlock some elusive mysteries at the cellular level. Overall, the findings of this study advance our understanding of this essential biological phenomenon and pave the way for future research in this field.

    Source:

    Journal reference:

    Fujita, J., et al. (2025). Structural basis for the interaction between the bacterial cell division proteins FtsZ and ZapA. Nature Communications. doi.org/10.1038/s41467-025-60940-w.

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  • Teeth marks suggest ‘terror bird’ was killed by reptile 13 million years ago

    Teeth marks suggest ‘terror bird’ was killed by reptile 13 million years ago

    Victoria Gill

    Science correspondent, BBC News

    Link et al/Biology Letters The image shows an artist's impression of a terror bird being attacked by a caiman, a large crocodile-like predator. The caiman is emerging from a river and grabbing the panicked bird by its leg. This depicts a scene that scientists believe could have taken place 13 million years ago in Colombia. Link et al/Biology Letters

    The researchers say the terror bird did not survive the encounter

    Teeth marks made on the leg bone of a large avian reptile known as a terror bird 13 million years ago suggest an even bigger predator may have killed it, scientists say.

    Terror birds were top predators – they could be taller than a human and had powerful legs and hooked, flesh-ripping beaks.

    Palaeontologists in Colombia matched teeth marks on the fossilised leg bone of one of these fearsome birds to a caiman, or a crocodile-like reptile.

    3D digital scans of the bites allowed the scientists to reconstruct what they believe was a “battle to the death” that the terror bird did not survive.

    Link et al/Biology Letters The image shows the digital scan of a crocodile skull biting into a small leg bone. The bone that is being bitten into is based on a 3D scan of the 13 million year old fossilised bone from a terror bird.  Link et al/Biology Letters

    The researchers scanned the teeth marks in the leg bone and compared it with skulls and teeth of crocodile-like predators

    The new study, published in the journal Biology Letters, compared the size and shape of the teeth marks to the skulls and teeth of crocodile-like predators in museum collections.

    It provides rare evidence, the researchers say, of an interaction between two extinct top predators at the time.

    The leg bone the scientists studied was first unearthed more than 15 years ago in Colombia’s Tatacoa Desert.

    When the bird lived in the swamps of that area 13 million years ago, it would have been about 2.5m tall and would have used its legs and beak to hold down and rip at its prey.

    What the scientists are not able to prove conclusively is whether this particular, unfortunate terror bird was killed in the attack, or if the caiman scavenged its remains.

    “There is no sign of healing in the bite marks on the bone,” explained lead researcher Andres Link from the Universidad de Los Andes in Bogotá, Colombia.

    “So if it wasn’t already dead, it died in the attack. That was the last day that bird was on this planet – then a piece of its leg bone was found 13 million years later.”

    Andres Link The image shows a chunk of fossilised bone from a terror bird's leg. There are two holes visible in the bone - puncture marks left by the teeth of a predatory reptile. Andres Link

    The teeth marks are clearly visible on the piece of leg bone

    The Tatacoa Desert is home to rich deposits of fossils from an epoch known as the Middle Miocene.

    At that time, it was a humid swamp, where river sediments trapped and fossilised the bones of dead animals, resulting in the preserved remains found there today.

    This particular bone was first discovered about 15 years ago by local fossil collector César Augusto Perdomo.

    The Colombian scientists worked closely with Mr Perdomo, studying and cataloging fossils that he has gathered in his museum. It was when scientists were working in the museum that they realised that this fist-sized piece of leg bone came from a terror bird.

    That was an exciting discovery – terror bird fossils are rare. But Dr Link and his colleagues were also fascinated by the puncture marks in the bone, which had clearly been made by the teeth of another powerful predator.

    Andres Link The image shows a fossil collector at a dusty site in Colombia. The man wears a red shirt and a wide-brimmed hat to protect him from the sun. His feet are bare and he is examining the ground carefully for fossils. Andres Link

    César Augusto Perdomo has been collecting fossils since he was a child

    This new analysis of the marks revealed that they most closely match an extinct caiman species called Purussaurus neivensis, a crocodilian that would have been up to five metres long.

    The researchers say it would have ambushed its prey from the water’s edge, much like crocodiles and caimans do today.

    “I would imagine it was waiting for prey to to be nearby,” said Dr Link.

    If this was indeed a battle between two apex predators, Dr Link says that provides insight into an ancient ecosystem. It reveals that ferocious terror birds were much more vulnerable to predators than previously thought.

    “Every piece of a body helps us to understand so much about life on the planet in the past,” Dr Link told BBC News.

    “That’s something that amazes me – how one tiny bone can complete the story.”

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  • Earth-sized planet found that would instantly kill anyone visiting

    Earth-sized planet found that would instantly kill anyone visiting

    (Web Desk) – A new Earth-sized planet has been discovered in a faraway constellation – and it would kill any astronaut who dare travel there.

    Some 117.4 light-years away from Earth, scientists have stumbled across a nightmarish alien world where the planet’s surface is likely molten.

    The planet, dubbed TOI-2431, orbits quite close to its nearest star over a very short period, resulting in a high surface temperature.

    Unlike Earth, which has an orbital period of 365 days, TOI-2431 orbits its star in only 5.4 hours – making it one of the shortest period exoplanets ever discovered.

    The alien world, located in constellation Cetus, is thought to have a surface temperature of about 1,700C (3092F).

    Anything that lands there would be immediately incinerated.

    The international team of astronomers, led by Kaya Han Taş of the University of Amsterdam in the Netherlands, detected the new exoplanet orbiting a nearby star using Nasa’s Transiting Exoplanet Survey Satellite (TESS).

    “We have confirmed the ultra-short period planet TOI-2431 b using a combination of photometric transit data from TESS, precise radial velocity observations with the NEID and HPF spectrographs, and ground-based speckle imaging with the NESSI instrument,” researchers wrote in the new research paper.

    The Nasa tool monitors about 200,000 bright stars near Earth, scanning for hidden planets that might cause any blips of light as they pass their star.

    Just last week, researchers revealed they used TESS to follow a repetitive flicker of starlight to a new ‘Super Earth’ 154 light-years away.

    Since its launch in April 2018, the satellite has identified more than 7,600 possible exoplanets – which are nicknamed TESS Objects of Interest, or TOI.

    Exactly 638 of these have been confirmed as alien worlds so far.

    The planet’s host star is only about two-thirds the size and mass of our Sun, and appears to be pulling the planet towards a fiery death.

    Researchers estimated that the planet has a tidal decay timescale of about 31 million years – which is fairly short in the grand schemes of the universe.

    Tidal decay causes a planet’s orbit to gradually shrink and spiral towards its host star – eventually leading to its destruction.

    The 2billion-year-old host star, which researchers believe is roughly double the temperature of its nearby planet, will eventually collide with the planet.

    Researchers hope they can secure time with the James Webb Space Telescope (JWST) to study TOI-2431 b more closely.

    Doing so could shed more light on the planet’s surface composition, and may answer the question of whether or not it has an atmosphere.

    The $10 billion telescope discovered its first-ever exoplanet just last month, but has been used to analyse others on its journey through space. 


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  • FAA says power outage forced postponement of SpaceX TRACERS launch – news.cgtn.com

    FAA says power outage forced postponement of SpaceX TRACERS launch – news.cgtn.com

    1. FAA says power outage forced postponement of SpaceX TRACERS launch  news.cgtn.com
    2. NASA’s TRACERS Mission Targeting Launch on July 22  NASA Science (.gov)
    3. SpaceX launch rescheduled due to Santa Barbara power outage  KTLA
    4. NASA’s TRACERS Mission Scrubbed, July 23 Next Attempt  NASA (.gov)
    5. SpaceX Launch Could Cause Southern Californians to Hear a Sonic Boom on Wednesday  LAmag

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  • Astronaut Fitness Gets a Boost with Adaptive Harness Design

    Astronaut Fitness Gets a Boost with Adaptive Harness Design

    What new exercise methods can be devised for astronauts in space under microgravity conditions? This is what a recent study conducted submitted to the 2025 Technology Collaboration Center’s (TCC) Wearables Workshop and University Challenge hopes to address as a team of Rice University engineering students developed a new type of space exercise harness that could make exercising under microgravity easier and more comfortable.

    For the study, the students designed and developed a customizable astronaut exercise harness that measures load distribution at pressure points (shoulders, hips, etc.) to mitigate injuries from body shifts during exercise and temperature and humidity changes during exercise. Along with improved technology compared to current harnesses, the new harness also provides an enhanced level of comfort that prevents unnecessary skin abrasions.

    “This challenge gave us the freedom to innovate and explore possibilities beyond the current harness technology,” said Emily Yao, a Rice undergraduate and part of the five-member team comprised of four undergraduates and one graduate student that developed the harness. “I’m especially proud of how our team worked together to build a working prototype that not only has real-world impact but also provides a foundation that NASA and space companies can build and iterate upon. This makes the entire experience incredibly rewarding. It’s moments like these that remind me why I love designing with and for people.”

    In the end, the harness was chosen as the winner for the Best Challenge Response Award, thus potentially paving the way for this harness to be improved function and use, and possibly real-world use by astronauts in space. Along with improving exercise and physical health, this harness could provide a boost to astronaut mental health due to its simplicity and customizable design.

    Astronauts exercising in space has been happening almost since the beginning of the Space Age, as Gemini astronauts used off-the-shelf exercise equipment to combat the effects of microgravity. Beginning on Apollo 7, NASA began using the Exer-Genie Exerciser, as Apollo 7 was the first mission to exhibit enough room inside the spacecraft for astronauts to conduct exercises.

    The Exer-Genie consisted of a metal shaft and nylon rope that the astronauts could adjust to their preferences. To use the Exer-Genie, astronauts would pull on the rope, resulting in friction and resistance, enabling them to perform more than 100 basic exercises designed to maintain muscle mass while combating microgravity. The Exer-Genie was equipped with all crewed Apollo missions (Apollo 7 through 17) but were actually used by the astronauts on Apollo 7, 8, 9, 11. 12. And 16.

    This study comes as NASA plans to send astronauts back to the Moon for the first time since Apollo 17 in 1972 with the goal of establishing a permanent human settlement on the lunar surface. One of the goals of a lunar settlement will be to test technologies for a future crewed mission to Mars as part of NASA’s Moon to Mars Architecture. Following the successful uncrewed Artemis I mission in November 2022, the crewed Artemis II mission is scheduled for early 2026 and will send four astronauts around the Moon, mirroring Apollo 8’s historic flight. This will be followed by Artemis III, which is scheduled to occur in mid-2027 with a four-person crew and landing two on the lunar surface.

    Sending astronauts to the Moon and Mars demonstrates how humans will endure longer periods of reduced gravity on both the Moon and Mars at one-sixth and one-third gravity of Earth, respectively. While this isn’t full microgravity as experienced on the International Space Station (ISS), reduced gravity still results in decreased muscle mass and bone loss that astronauts need to maintain to continue their mission, but especially when re-adapting to Earth’s gravity when they come home.

    How will this new exercise harness help astronauts in space in the coming years and decades? Only time will tell, and this is why we science!

    As always, keep doing science & keep looking up!

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