Lifeboat Foundation

Circa 2011

It sounds like a late-night infomercial: Kill germs and clean surfaces with nothing more than water and a few volts of electricity! Pay pennies a gallon! Strong enough to kill germs but gentle on your skin!

The use of electricity and water to clean and disinfect has been embraced by some food and hospitality businesses looking to save money and go green by swapping out conventional products.

Continue reading “Electrified water lets cleaners ditch the bleach” »

When you put these three factors together—the bounty of technological advances, the compressed restructuring timetable due to covid-19, and an economy finally running at full capacity—the ingredients are in place for a productivity boom. This will not only boost living standards directly, but also frees up resources for a more ambitious policy agenda.

AI and other digital technologies have been surprisingly slow to improve economic growth. But that could be about to change.

COVID 19 pandemic, automation and 6G could end the metropolitan era from building high sky scrapers for companies. Companies can operate like a network from home to home without going to office. This will help a lot to bring down Urban Heat Islands and make our cities more efficient in transportation and communication to send the data even faster.

Tom Marzetta is the director of NYU Wireless, New York University’s research center for cutting-edge wireless technologies. Prior to joining NYU Wireless, Marzetta was at Nokia Bell Labs, where he developed massive MIMO. Massive MIMO (short for “multiple-input multiple-output”) allows engineers to pack dozens of small antennas into a single array. The high number of antennas means more signals can be sent and received at once, dramatically boosting a single cell tower’s efficiency.

Massive MIMO is becoming an integral part of 5G, as is an independent development that came out of NYU Wireless by the center’s founding director Ted Rappaport: Millimeter waves. And now the professors and students at NYU Wireless are already looking ahead to 6G and beyond.

Continue reading “Heres What 6G Will Be, According to the Creator of Massive MIMO” »

A team of researchers from the University of Sydney, the ARC-Plant Protection Research Institute and York University, has found that workers in a species of honeybee found in South Africa reproduce by making near-perfect clones of themselves. In their paper published in Proceedings of the Royal Society B, the group describes their study of the bees and what they learned about them.

Prior research has found that some creatures reproduce through parthenogenesis, in which individuals reproduce without mating. This form of reproduction has the advantage of not wasting time and energy on mating and the gene pool remains undiluted. The downside, of course, is loss of genetic diversity, which helps species survive in changing conditions. Prior research has also shown that for most species, parthenogenesis is a less-than-perfect way to produce offspring. This is because some tiny bit of genetic material is generally mixed wrong—these mistakes, known as recombinations, can lead to birth defects or non-productive eggs. In this new effort, the researchers have found a kind of honeybee that has developed a way to avoid recombinations.

The researchers found that South African Cape honeybee queens reproduce sexually, but the workers reproduce asexually. They then conducted a small experiment—they affixed tape to the reproductive organs of a queen, preventing males from mating with her, and then allowed both her and the worker bees in the same hive to reproduce asexually. They then tested the degree of recombination in both. They found that offspring of the queen had approximately 100 times as much recombination as the worker bees. Even more impressive, the offspring of the worker bees were found to be nearly identical clones of their parent. More testing showed that one line of worker bees in the hive had been cloning themselves for approximately 30 years—a clear sign that workers in the hive were not suffering from birth defects or an inability to produce viable offspring. It also showed that they have evolved a means for preventing recombination when they reproduce.

A team of scientists at the University of Sussex have for the first time built a modular quantum brain scanner, and used it to record a brain signal. This is the first time a brain signal has been detected using a modular quantum brain sensor anywhere in the world. It’s a major milestone for all researchers working on quantum brain imaging technology because modular sensors can be scaled up, like Lego bricks. The team have also connected two sensors like Lego bricks, proving that whole-brain scanning using this method is within reach—as detailed in their paper, which is published today in pre-print. This has not been possible with the currently commercially available quantum brain sensors from the United States.

These modular devices work like play bricks in that they can be connected together. This opens up the potential for whole–brain scanning using quantum technology, and potential advances for neurodegenerative diseases like Alzheimer’s.

The device, which was built at the Quantum Systems and Devices laboratory at the university, uses ultra-sensitive quantum sensors to pick up these tiniest of magnetic fields to see inside the brain in order to map the neural activity.

Google has helped create the most detailed map yet of the connections within the human brain. It reveals a staggering amount of detail, including patterns of connections between neurons, as well as what may be a new kind of neuron.

The brain map, which is freely available online, includes 50000 cells, all rendered in three dimensions. They are joined together by hundreds of millions of spidery tendrils, forming 130 million connections called synapses. The data set measures 1.4 petabytes, roughly 700 times the storage capacity of an average modern computer.

The data set is so large that the researchers haven’t studied it in detail, says Viren Jain at Google Research in Mountain View, California. He compares it to the human genome, which is still being explored 20 years after the first drafts were published.

While DNA provides the genetic recipe book for biological form and function, it is the job of the body’s proteins to carry out the complex commands dictated by DNA’s genetic code.

Stuart Lindsay, a researcher at the Biodesign Institute at ASU, has been at the forefront of efforts to improve rapid DNA sequencing and has more recently applied his talents to explore the much thornier problem of sequencing protein molecules, one molecule at a time.

In a new overview article, Lindsay’s efforts are described along with those of international colleagues, who are applying a variety of innovative strategies for protein sequencing at the single-cell, and even single-molecule level.

Cells contain machinery that duplicates DNA into a new set that goes into a newly formed cell. That same class of machines, called polymerases, also build RNA messages, which are like notes copied from the central DNA repository of recipes, so they can be read more efficiently into proteins. But polymerases were thought to only work in one direction DNA into DNA or RNA. This prevents RNA messages from being rewritten back into the master recipe book of genomic DNA. Now, Thomas Jefferson University researchers provide the first evidence that RNA segments can be written back into DNA, which potentially challenges the central dogma in biology and could have wide implications affecting many fields of biology.

“This work opens the door to many other studies that will help us understand the significance of having a mechanism for converting RNA messages into DNA in our own cells,” says Richard Pomerantz, Ph.D., associate professor of biochemistry and molecular biology at Thomas Jefferson University. “The reality that a human polymerase can do this with high efficiency, raises many questions.” For example, this finding suggests that RNA messages can be used as templates for repairing or re-writing genomic DNA.

The work was published June 11th in the journal Science Advances.

Scientists have successfully grown liver tissue capable of functioning for 30 days in the lab as part of NASA’s Vascular Tissue Challenge.

In 2016, NASA put forth this competition to find teams that could “create thick, vascularized human organ tissue in an in-vitro environment to advance research and benefit medicine on long-duration missions and on Earth,” according to an agency challenge description. Today (June 9), the agency announced not one, but two winners of the challenge.