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The 14 “Carbon Bombs” That Are About To Blow Up The Planet

These projects to increase production of fossil fuels are being planned around the world. But if all of them come to fruition, it may be the last fossil fuels we produce, because the combined effect will be to raise the planet’s temperature disastrously.

If you believe in the possibilities of corporate responsibility—or for that matter, basic human kindness—you probably shouldn’t read Greenpeace’s latest climate change report. It might shake your faith.

Why? Because its conclusion is so stark and so simple, and yet so widely and willfully ignored: If we go ahead with 14 major fossil fuel projects now on the drawing board (you can see them above), we’ll have a good chance of destroying the world as we know it. Or, to put it less emotionally: We’ll sail right through carbon limits most scientists agree are safe for the atmosphere.

Take a look at the slide show for a graphic sense of the danger. From coal production in Australia, China, and Indonesia, to deepwater oil projects in Brazil and the Arctic, to tar sands in Canada and Venezuela, to shale gas and conventional gas in the U.S. and the Caspian Sea, the world is set for a big push on the dirtiest forms of energy development. Together, Greenpeace says the projected output will increase emissions 20% by 2020, thus “locking in” long-term temperature increases in the 5 to 6 degrees Celsius range. Scientists normally call 2 degrees a relatively safe limit—and until recently that was the consensus in the international community as well.

“With total disregard for this unfolding global disaster, the fossil fuel industry is planning 14 massive coal, oil, and gas projects that would produce as much new carbon dioxide (CO2) emissions in 2020 as the entire U.S., and delay action on climate change for more than a decade,” the report says.

Greenpeace says the 14 developments would produce 54,674 million tons of coal, 29,400 billion cubic meters of natural gas, and 260,000 million barrels of oil—but add 330 billion tons of CO2-equivalent emissions by 2050 (see here for the methodology). To stay within the 2-degree increase, emissions have to start falling before 2015, which means canceling, rather than rushing ahead, with some of the plans on the table. That doesn’t seem likely—but it is the wide consensus not only of the enviro-lobby, but of plenty of sensible people who’ve studied the issue.

[All Images: Shutterstock]

BEN SCHILLER is a staff writer for Co.Exist, and also contributes to the FT, and Yale e360. 

UK Scientists Print Human Stem Cells with a 3D Printer

A group of scientists in the UK and Scotland have successfully printed human stem cells using a “valve-based cell printer” which utilizes bio-inks to fabricate clusters of viable stem cells that can become any type of cell in your body.

UK Scientists Print Human Stem Cells with a 3D Printer

Your Guide to the Next 150 Years. By Joshua M Brown

(by odds of occurrence)

Your Guide to the Next 150 Years. By

(by odds of occurrence)


Twin attack could deliver universal flu vaccine. By Debora MacKenzie




A UNIVERSAL vaccine. It is the stuff of dreams for flu scientists, but it could be within reach if a new type of vaccine that elicits an immune response from white blood cells is combined with traditional vaccines.
Every year, between 250,000 and 500,000 people of all ages die worldwide after getting seasonal flu, partly because few people are vaccinated for it. When a novel human flu evolves in pigs or poultry and becomes pandemic, the numbers can be even higher. The solution is better vaccines for people and animals.
Flu comes back every year because when you catch it or are vaccinated, your immune system is only trained to identify the flu’s large surface proteins. These proteins change from year to year, allowing flu to strike again if you haven’t had an updated   attempts have been vaccines designed to make us produce antibodies, aimed not at flu’s surface proteins, but at internal proteins that are the same in all flu viruses. Success has been mixed. But there is another arm to the immune system. White blood cells called T-cells tend to attack a wider range of invaders than antibodies. If a vaccine sensitises them to internal flu proteins, they could potentially kill all types of flu.
Earlier this year, Sarah Gilbert and colleagues at the University of Oxford equipped the virus used in the smallpox vaccine, which stimulates this cell-mediated immunity, with two proteins common to all flu viruses. They reported that this vaccine prevented symptoms in some people experimentally infected with flu, and those that did get sick had milder symptoms.
Now Colin Butter and colleagues at the Institute for Animal Health in Compton, UK, have tested that vaccine, and a similar one made of a different live virus, in chickens (Vaccine, doi.org/jz6). Just as in people, it did not prevent infection, but the birds’ T-cells responded strongly, and less of the virus was passed on.
Neither result sounds very impressive. But, says Butter, the key will be combining these vaccines with the classic kind that elicits antibodies. Gilbert reports that her team has tested such a combination in people, and has seen cell-mediated immunity to the universal proteins, as well as antibodies to specific surface proteins.
Such a combination could be more than the sum of its parts. In chickens, for example, antibodies could knock out the main virus, while T-cells mop up the variants that evade the antibodies and allow the virus to keep spreading - and evolving. “We could finally get vaccines that stop viral spread completely,” says Butter.
The “universal” proteins would also give chickens and humans some protection against novel flu viruses. And because they work against all flu, such vaccines can be stockpiled to prepare for pandemics. “I’d love to have a stockpile of vaccine with both antibody and cell-mediated capabilities,” says Thomas Reichert of the Entropy Research Institute in Lincoln, Massachusetts. This gives us a chance to beat an adversary we’ve been defeated by time and again. Or as Reichert puts it: “Now that might bring flu to the negotiating table.”



From issue 2896 of New Scientist magazine, page 10.

Twin attack could deliver universal flu vaccine. By Debora MacKenzie

A UNIVERSAL vaccine. It is the stuff of dreams for flu scientists, but it could be within reach if a new type of vaccine that elicits an immune response from white blood cells is combined with traditional vaccines.

Every year, between 250,000 and 500,000 people of all ages die worldwide after getting seasonal flu, partly because few people are vaccinated for it. When a novel human flu evolves in pigs or poultry and becomes pandemic, the numbers can be even higher. The solution is better vaccines for people and animals.

Flu comes back every year because when you catch it or are vaccinated, your immune system is only trained to identify the flu’s large surface proteins. These proteins change from year to year, allowing flu to strike again if you haven’t had an updated   attempts have been vaccines designed to make us produce antibodies, aimed not at flu’s surface proteins, but at internal proteins that are the same in all flu viruses. Success has been mixed. But there is another arm to the immune system. White blood cells called T-cells tend to attack a wider range of invaders than antibodies. If a vaccine sensitises them to internal flu proteins, they could potentially kill all types of flu.

Earlier this year, Sarah Gilbert and colleagues at the University of Oxford equipped the virus used in the smallpox vaccine, which stimulates this cell-mediated immunity, with two proteins common to all flu viruses. They reported that this vaccine prevented symptoms in some people experimentally infected with flu, and those that did get sick had milder symptoms.

Now Colin Butter and colleagues at the Institute for Animal Health in Compton, UK, have tested that vaccine, and a similar one made of a different live virus, in chickens (Vaccinedoi.org/jz6). Just as in people, it did not prevent infection, but the birds’ T-cells responded strongly, and less of the virus was passed on.

Neither result sounds very impressive. But, says Butter, the key will be combining these vaccines with the classic kind that elicits antibodies. Gilbert reports that her team has tested such a combination in people, and has seen cell-mediated immunity to the universal proteins, as well as antibodies to specific surface proteins.

Such a combination could be more than the sum of its parts. In chickens, for example, antibodies could knock out the main virus, while T-cells mop up the variants that evade the antibodies and allow the virus to keep spreading - and evolving. “We could finally get vaccines that stop viral spread completely,” says Butter.

The “universal” proteins would also give chickens and humans some protection against novel flu viruses. And because they work against all flu, such vaccines can be stockpiled to prepare for pandemics. “I’d love to have a stockpile of vaccine with both antibody and cell-mediated capabilities,” says Thomas Reichert of the Entropy Research Institute in Lincoln, Massachusetts. This gives us a chance to beat an adversary we’ve been defeated by time and again. Or as Reichert puts it: “Now that might bring flu to the negotiating table.”

Issue 2896 of New Scientist magazine
  • From issue 2896 of New Scientist magazine, page 10.

NASA tries to convince us world won’t end

Biohackers And DIY Cyborgs Clone Silicon Valley Innovation. By Neal Ungerleider

A new breed of hobbyists, scientists, and entrepreneurs are working on echolocation implants, brain-controlled software programs, and even cybernetic rats. Their experiments will change the future of tech.

In basements, garages, startup spaces, and university laboratories, DIY researchers, scientists, programmers, and neurologists are collaborating on brain interfaces that can control video games with human thoughts. They’re growing flesh that’s augmented with transistors and implanting Bluetooth sensors under their own living skin to send vital signs to mobile phones. They’re growing in vitro edible “steaks” and leather without using living beings. They’re even helping severely disabled individuals “speak” using only their brainwaves. And most of them still consider this a hobby.

The grinders (DIY cybernetics enthusiasts) and their comrades in arms—biohackers working on improving human source code, quantified self enthusiasts who arm themselves with constant bodily data feeds, and independent DIY biotechnology enthusiasts—are moonlighting for now in basements, shared spaces, and makeshift labs. But they’re ultimately aiming to change the world. Think of how bionic legs like those belonging to Oscar Pistorius and cochlear implants that let the deaf hear have changed everyday life for so many people. Then multiply that by a million. A million people. And millions of dollars.

Not only has the new wave of do-it-yourself (DIY) cybernetics moved well beyond science fiction, it’s going to cause a business boom in the not-too-distant future.

West Coast biohackers and grinders were the pioneers of this tech-driven, California brand of utopianism. They’ve taken a big-tent approach to their goal of hacking humanity: Paleo diets and meditation are just as likely to figure into things as cybernetic finger implants or controlling computer apps with brainwaves. For biohackers everywhere, augmentation of humanity itself—whether through technology or more traditional methods—is the primary goal. Common conversation points include DIY cyborgs, the quantified self, and diet- and meditation-based improvement movements like Dave Asprey’s Bulletproof Executive or crowdsourced health projects like CureTogether.

But a growing community on the East Coast—in greater New York, Boston, and Pittsburgh—is synthesizing Silicon Valley’s entrepreneurial DNA for its unique innovation model. Experimentation and science here is not only an exercise in advancing humanity through tech but is often is applied toward creating viable cybernetic products for the market.

In New York City, biohackers are united by the extremely active Biohackers NYC Meetup group and several startups, incubators, and workspaces scattered across the outer boroughs.

When the Biohackers NYC group was founded in early 2012, “It was because most biohacker movements started on West Coast, and the East Coast was lagging behind. I lamented the lack of this on the East Coast,” group founder and psychiatrist Lydia Fazzio tells Fast Company. “Our intent was to cover the spectrum of biohacking from manipulating non-human genomes to also the body and the mind. It’s a holistic approach to the meaning of biohacking, whether technology or nutrition. However you get there, we all have the innate potential to be an optimal functioning human in society. Our question is: How do we get there?” 




In Brooklyn, a small “community biolab” called Genspace is home to approximately a dozen DIY biology experimenters whose work often involves the fusion of the living and the electronic. Classes are offered to the public in synthetic biology, which engineers living organisms as if they were biological machines. 

A workshop recently held at Genspace, Crude Control, showed how in-vitro meat and leather could be created via tissue engineering, and it explored the possibility of creating semi-living “products” from them. Although the Genspace workshop was for educational purposes, similar technologies are already being monetized elsewhere—Peter Thiel recently sank six figures into a startup that will make 3-D printed in vitro meat commercially available.
The teacher at the Crude Control workshop, Oron Catts, walked participants through “basic tissue culture and tissue engineering protocols, including developing some DIY tools and isolating cells from a bone we got from a local butcher.” Some of Catts’ previous projects include bioengineering a steak from pre-natal sheep cells (in his words, “steak grown from an animal that was not yet born”) and victimless leather grown from cell lines.

Just a few hours up I-95 at Harvard University, researchers have created the world’s first “cyborg flesh.” The university’s Lieber Research Group, led by Charles Lieber, has successfully created rat flesh that is seamlessly melded with a network of wires and transistors that monitor the individual behavior of each cell.



Lieber’s groundbreaking research integrated electrically active scaffolds into rat cardiomyocytes, or heart muscle cells. Incredibly small wires and transistors were embedded in scaffolding made with collagen and wires; using the cybernetic tissue, researchers could keep track of the minute behavior of cells during drug reactions. Harvard’s experiment is far more than just the weird science of creating cybernetic rats, though. In the future, projects built on this technology could be used to do away with animal or human testing for drugs, and to create cybernetic implants to repair damaged hearts.

Meanwhile, in Pittsburgh, Grindhouse Wetwares is an Internet-based collective of programmers, engineers, and scientists dedicated to “augmenting humanity using safe, affordable, open-source technology.” Many of Grindhouse’s members are currently based in Pittsburgh, which has become an impromptu nexus for DIY cybernetics enthusiasts. The organization’s current project is a literal —a cap with attached electrodes that stimulates the brain with electricity. Users are zapped with direct current via the electrodes, which allegedly engage certain brain states depending on placement.

Grindhouse has a business model that recalls that of early Silicon Valley companies like the original Apple of Steve Wozniak and Steve Jobs. The collective intentionally makes project plans available via Creative Commons licenses; customers can either pay Grindhouse to build their devices or they can make it at home for free.


Other projects from Grindhouse take the merger of human and machine even further. The Bottlenose is a device which transforms sonar, UV, Wi-Fi, or thermal information into a magnetic field that the user can then feel. End users can either receive an impromptu cybernetic implant in their finger or wear a haptic version of the device. Both the implanted version and the worn-on-body version physically stimulate the user when they walk past, say, a microwave or a wireless router. Much like the Thinking Cap, a Bottlenose can be constructed at home using the organization’s free schematics, or implants/wearable field detectors can be purchased online.



Another project, the Heleed, is a cybernetic medical tracking device. Users implant the Bic lighter-sized device in their body, which then automatically sends biomedical information to the Internet via a Bluetooth interface. The strictly experimental Heleed can also be programmed to display health warnings—sent to the recipient via an Android app—on the user’s skin with LED lights.

Heleed is expected to be released to the public in time for the holiday season. Grindhouse’s Lucas Dimoveo told Fast Company that the device currently records body temperature, heart rate, and time. Future versions will have additional sensors added; “the goal is to have your implant text your phone with health factoids like ‘Did you know that when you are on Jamaica Avenue between Van Wyck and Francis Lewis your blood pressure increases ___ mmHg?’” This end goal is not very dissimilar from several non-cybernetic products now making it to market, such as GPS-integrated asthma inhalers.

These implants have substantial real-life effects. Dimoveo described a few:
“In the lab one of our older laptops stopped working—sometimes it would recharge and other times it wouldn’t. It took [Grindhouse experimenters] Tim Cannon and Shawn Sarver all of five seconds to figure out what was going on just by running their hands from the extension cord up the power brick to the computer itself. The wire was giving off a field, but not the battery (which sadly meant I needed to get a new computer). There is no way I would have figured out the problem that fast.

“Our artist, Mike Seeler, has larger than average magnet implants in both hands. Traveling through New York City is a very different experience for the both of us. He is constantly discovering magnetic fields pouring out of the street, the subway, the bus, and buildings. He has even had a few dreams including his magnetic sense.”

“The only drawback to the magnet implant is that interacting with mundane machinery can cause people to recoil in shock at how much power is running through a wire or machine. I’ve seen a few people on the team walk by a live soldering station and recoil in surprise. An audible response to the effect of ‘whoa’ is usually uttered, along with a concerned look. Real emotional responses can be triggered by this implant.”


Biohackers first came into the public consciousness thanks to an August 2012 article on tech website The Verge, where author Ben Popper had one of Grindhouse’s cybernetic magnetic implants surgically placed in his thumb. The implant, made from the rare earth metal neodymium, allowed Popper to feel magnetic fields.
DIY cybernetics and the informal merger of human with machine attracts both professionals and dedicated hobbyists with unrelated day jobs. Two popular message boards, and DIYbio (which deals with the larger field of DIY biotechnology labs), serve as meeting points for researchers in the field. At BioArt Laboratories, a Dutch organization featured on DIYbio, art and music are made using cell cultures and biological materials. Meanwhile, users on biohack.me are contemplating the possibilities of subdermal bone conduction headphones and echolocation implants.

One of the biggest boom areas for the DIY cybernetics community is controlling software and applications with brain waves. Crucially, it is the one technology for which we currently have robust development tools and a price point which allows hobbyists to easily experiment. Brain-computer interfaces are increasingly commonplace; in their most common commercial incarnation, users control computer software—most frequently games or simple applications—with brainwave-reading electrodes.

Upstate New York is home to one of the best known brain-computer interface systems out there. BCI2000 was developed at the Wadsworth Center of the New York State Department of Health in Albany in order to create a framework for computer software to understand input from human brainwaves. Using BCI2000, developers have been able to create projects such as a blink-input computer typing system for the disabled and even brainwave-controlled robots. At the Wadsworth Center itself, research efforts on BCI are primarily focused on creating new communication methods for the severely disabled.

There is an undeniable science fiction factor to the idea of DIY cybernetics such as Ekso’s robotic exoskeleton for paraplegics. However, one important thing has to be remembered: Man and machine have been merging for a long time. Cochlear implants and bionic legs are just the latest in a long list of human augmentation that ranges from pacemakers to eyeglasses.

These technologies aren’t just for the future either; they’re being monetized and put to market on a mass scale today. Austrian firm g.tec released a product for patients with motor disabilities that lets them spell words using their brainwaves. Using the product, users who have severe difficulty communicating otherwise can attain a spelling rate of 5 to 10 letters per minute.




Two new consumer products also let ordinary folks—that is, ordinary folks with some money to burn—turn themselves into temporary cyborgs. Neurosky’s MindWave Mobile is a $130 brainwave-reading device for Android and iOS platforms. With the headset-like Bluetooth device, users can play simple proprietary games via their brainwaves—with no hand or gesture input required. Eight apps are included, such as shooters and “Choose Your Own Adventure”-style interactive movies. Rival firm Emotiv markets a brainwave-reading headset compatible with both proprietary games and standard PC games that retails for $299.

Crucially, both Emotiv and Neurosky make software development kits (SDKs) and APIs available to outside content producers. Both firms make the possibility of creating brain-controlled software more or less as simple as building an Android app. In other words, 20 or 30 years from now, we’ll likely look back on the biohacker and grinder communities like we currently look back on Silicon Valley of the early to mid 1970s or Stanford or Harvard in the ’90s, places and times when dedicated hobbyists and small businesspeople built homebrewed computers and software in garages and dorm rooms—and founded companies such as Apple, Google, and Facebook.

Should Oscar Pistorius’ Prosthetic Legs Disqualify Him from the Olympics? By Rose Eveleth

oscar pistorius, prosthetic legs, olympics. Wikimedia Commons/Erik van LeeuwenImage: Wikimedia Commons/Erik van Leeuwen

Runners who’ve faced off against Oscar Pistorius say they know when the South African is closing in on them from behind. They hear a distinctive clicking noise growing louder, like a pair of scissors slicing through the air—the sound of Pistorius’s Flex-Foot Cheetah prosthetic legs.

It’s those long, J-shaped, carbon-fiber lower legs—and the world-class race times that come with them—that have some people asking an unpopular question: Does Pistorius, the man who has overcome so much to be the first double amputee to run at an Olympic level, have an unfair advantage? Scientists are becoming entwined in a debate over whether Pistorius should be allowed to compete in the 2012 London Games.

Pistorius was born without fibulas, one of the two long bones in the lower leg. He was unable to walk as a baby, and at 11 months old both of his legs were amputated below the knee. But the growing child didn’t let his disability slow him down. At age 12 he was playing rugby with the other boys, and in 2005, at age 18, he ran the 400-meter race in 47.34 seconds at the South African Championships, sixth best. Now 25, the man nicknamed the “Blade Runner” has qualified for the 2012 Summer Olympics in London, just three weeks before the games were to begin. But should he be allowed to compete?

The question seems preposterous. How could someone without lower legs possibly have an advantage over athletes with natural legs? The debate took a scientific turn in 2007 when a German team reported that Pistorius used 25 percent less energy than natural runners. The conclusion was tied to the unusual prosthetic made by an Icelandic company called Össur. The Flex-Foot Cheetah has become the go-to running prosthetic for Paralympic (and, potentially Olympic) athletes. “When the user is running, the prosthesis’s J curve is compressed at impact, storing energy and absorbing high levels of stress that would otherwise be absorbed by a runner’s ankle, knee, hip and lower back,” explains Hilmar Janusson, executive vice president of research and development at Össur. The Cheetah’s carbon-fiber layers then rebound off the ground in response to the runner’s strides.

After the German report was released, the International Association of Athletics Federations (IAAF) banned Pistorius from competing. Pistorius hired Jeffrey Kessler, a high-powered lawyer who’s represented athletes from the National Basketball Association and National Football League. It soon became clear that the IAAF’s study was very poorly designed, so when Pistorius’s team asked for a new study they got it. Soon scientists gathered at Rice University to figure out just what was going on with Pistorius’s body.

The scientific team included Peter Weyand, a physiologist at Southern Methodist University who had the treadmills needed to measure the forces involved in sprinting. Rodger Kram, at the University of Colorado at Boulder, was a track and field fan who studied biomechanics. Hugh Herr, a double amputee himself, was a renowned biophysicist. The trio, and other experts, measured Pistorius’s oxygen consumption, his leg movements, the forces he exerted on the ground and his endurance. They also looked at leg-repositioning time—the amount of time it takes Pistorius to swing his leg from the back to the front.

After several months the team concluded in a paper for The Journal of Applied Physiology that Pistorius was “physiologically similar but mechanically dissimilar” to someone running with intact legs. He uses oxygen the same way natural-legged sprinters do, but he moves his body differently.

Read on

Star Trek’s William Shatner explains the hair raising descent of the Mars Science Laboratory and its mission to explore the strange ‘red’ world
Credit: NASA

Are these the brain cells that give us consciousness? By Caroline Williams


The brainiest creatures share a secret – an odd kind of brain cell involved in emotions and empathy that may have accidentally made us conscious

THE origin of consciousness has to be one of the biggest mysteries of all time, occupying philosophers and scientists for generations. So it is strange to think that a little-known neuroscientist called Constantin von Economo might have unearthed an important clue nearly 90 years ago.

When he peered down the lens of his microscope in 1926, von Economo saw a handful of brain cells that were long, spindly and much larger than those around them. In fact, they looked so out of place that at first he thought they were a sign of some kind of disease. But the more brains he looked at, the more of these peculiar cells he found - and always in the same two small areas that evolved to process smells and flavours.

Von Economo briefly pondered what these “rod and corkscrew cells”, as he called them, might be doing, but without the technology to delve much deeper he soon moved on to more promising lines of enquiry.

Little more was said about these neurons until nearly 80 years later when, Esther Nimchinsky and Patrick Hof at Mount Sinai University in New York also stumbled across clusters of these strange-looking neurons. Now, after more than a decade of functional imaging and post-mortem studies, we are beginning to piece together their story. Certain lines of evidence hint that they may help build the rich inner life we call consciousness, including emotions, our sense of self, empathy and our ability to navigate social relationships.

Many other big-brained, social animals also seem to share these cells, in the same spots as the human brain. A greater understanding of the way these paths converged could therefore tell us much about the evolution of the mind.

Admittedly, to the untrained eye these giant brain cells, now known as von Economo neurons (VENs), don’t look particularly exciting. But to a neuroscientist they stand out like a sore thumb. For one thing, VENs are at least 50 per cent, and sometimes up to 200 per cent, larger than typical human neurons. And while most neurons have a pyramid-shaped body with a finely branched tree of connections called dendrites at each end of the cell, VENs have a longer, spindly cell body with a single projection at each end with very few branches (see diagram). Perhaps they escaped attention for so long because they are so rare, making up just 1 per cent of the neurons in the two small areas of the human brain: the anterior cingulate cortex (ACC) and the fronto-insular (FI) cortex.

Their location in those regions suggests that VENs may be a central part of our mental machinery, since the ACC and FI are heavily involved in many of the more advanced aspects of our inner lives. Both areas kick into action when we see socially relevant cues, be it a frowning face, a grimace of pain or simply the voice of someone we love. When a mother hears a baby crying, both regions respond strongly. They also light up when we experience emotions such as love, lust, anger and grief. For John Allman, a neuroanatomist at the California Institute of Technology in Pasadena, this adds up to a kind of “social monitoring network” that keeps track of social cues and allows us to alter our behaviour accordingly (Annals of the New York Academy of Sciences, vol 1225, p 59).

The two brain areas also seem to play a key role in the “salience” network, which keeps a subconscious tally of what is going on around us and directs our attention to the most pressing events, as well as monitoring sensations from the body to detect any changes (Brain Structure and FunctionDOI: 10.1007/s00429-012-0382-9).

What’s more, both regions are active when a person recognises their reflection in the mirror, suggesting that these parts of the brain underlie our sense of self - a key component of consciousness. “It is the sense of self at every possible level - so the sense of identity, this is me, and the sense of identity of others and how you understand others. That goes to the concept of empathy and theory of mind,” says Hof.

To Bud Craig, a neuroanatomist at Barrow Neurological Institute in Phoenix, Arizona, it all amounts to a continually updated sense of “how I feel now”: the ACC and FI take inputs from the body and tie them together with social cues, thoughts and emotions to quickly and efficiently alter our behaviour (Nature Reviews Neuroscience, vol 10, p 59).

This constantly shifting picture of how we feel may contribute to the way we perceive the passage of time. When something emotionally important is happening, Craig proposes, there is more to process, and because of this time seems to speed up. Conversely, when less is going on we update our view of the world less frequently, so time seems to pass more slowly.

VENs are probably important in all this, though we can only infer their role through circumstantial evidence. That’s because locating these cells, and then measuring their activity in a living brain hasn’t yet been possible. But their unusual appearance is a signal that they probably aren’t just sitting there doing nothing. “They stand out anatomically,” says Allman, “And a general proposition is that anything that’s so distinctive looking must have a distinct function.”

Fast thinking

In the brain, big usually means fast, so Allman suggests that VENs could be acting as a fast relay system - a kind of social superhighway - which allows the gist of the situation to move quickly through the brain, enabling us to react intuitively on the hop, a crucial survival skill in a social species like ours. “That’s what all of civilisation is based on: our ability to communicate socially, efficiently,” adds Craig.

A particularly distressing form of dementia that can strike people as early as their 30s supports this idea. People who develop fronto-temporal dementia lose large numbers of VENs in the ACC and FI early in the disease, when the main symptom is a complete loss of social awareness, empathy and self-control. “They don’t have normal empathic responses to situations that would normally make you disgusted or sad,” says Hof. “You can show them horrible pictures of an accident and they just don’t blink. They will say ‘oh, yes, it’s an accident’.”

Post-mortem examinations of the brains of people with autism also bolster the idea that VENs lie at the heart of our emotions and empathy. According to one recent study, people with autism may fall into two groups: some have too few VENs, perhaps meaning that they don’t have the necessary wiring to process social cues, while others have far too many (Acta Neuropathologica, vol 118, p 673). The latter group would seem to fit with one recent theory of autism, which proposes that the symptoms may arise from an over-wiring of the brain. Perhaps having too many VENs makes emotional systems fire too intensely, causing people with autism to feel overwhelmed, as many say they do.

Another recent study found that people with schizophrenia who committed suicide had significantly more VENs in their ACC than schizophrenics who died of other causes. The researchers suggest that the over-abundance of VENs might create an overactive emotional system that leaves them prone to negative self-assessment and feelings of guilt and hopelessness (PLoS One, vol 6, p e20936).

VENs in other animals provide some clues, too. When these neurons were first identified, there was the glimmer of hope that we might have found one of the key evolutionary changes, unique to humankind, that could explain our social intelligence. But the earliest studies put paid to that kind of thinking, when VENs turned up in chimpanzees and gorillas. In recent years, they have also been found in elephants and some whales and dolphins.

Like us, many of these species live in big social groups and show signs of the same kind of advanced behaviour associated with VENs in people. Elephants, for instance, display something that looks a lot like empathy: they work together to help injured, lost or trapped elephants, for example. They even seem to show signs of grief at elephant “graveyards” (Biology Letters, vol 2, p 26). What’s more, many of these species can recognise themselves in the mirror, which is usually taken as a rudimentary measure of consciousness. When researchers daub paint on an elephant’s face, for instance, it will notice the mark in the mirror and try to feel the spot with its trunk. This has led Allman and others to speculate that von Economo neurons might be a vital adaptation in large brains for keeping track of social situations - and that the sense of self may be a consequence of this ability.

Yet VENs also crop up in manatees, hippos and giraffes - not renowned for their busy social lives. The cells have also been spotted in macaques, which don’t reliably pass the mirror test, although they are social animals. Although this seems to put a major spanner in the works for those who claim that the cells are crucial for advanced cognition, it could also be that these creatures are showing the precursors of the finely tuned cells found in highly social species. “I think that there are homologues of VENs in all mammals,” says Allman. “That’s not to say they’re shaped the same way but they are located in an analogous bit of cortex and they are expressing the same genes.”

It would make sense, after all, that whales and primates might both have recycled, and refined, older machinery present in a common ancestor rather than independently evolving the same mechanism. Much more research is needed, however, to work out the anatomical differences and the functions of these cells in the different animals.

That work might even help us understand how these neurons evolved in the first place. Allman already has some ideas about where they came from. Our VENs reside in a region of the brain that evolved to integrate taste and smell, so he suggests that many of the traits now associated with the FI evolved from the simple act of deciding whether food is good to eat or likely to make your ill. When reaching that decision, he says, the quicker the “gut” reaction kicks in the better. And if you can detect this process in others, so much the better.

“One of the important functions that seems to reside in the FI has to do with empathy,” he says. “My take on this is that empathy arose in the context of shared food - it’s very important to observe if members of your social group are becoming ill as a result of eating something.” The basic feeding circuity, including the rudimentary VENs, may then have been co-opted by some species to work in other situations that involve a decision, like working out if a person is trustworthy or to be avoided. “So when we have a feeling, whether it be about a foodstuff or situation or another person, I think that engages the circuitry in the fronto-insular cortex and the VENS are one of the outputs of that circuitry,” says Allman.

Allman’s genetics work suggests he may be on to something. His team found that VENs in one part of the FI are expressing the genes for hormones that regulate appetite. There are also a lot of studies showing links between smell and taste and the feelings of strong emotions. Our physical reaction to something we find morally disgusting, for example, is more or less identical to our reaction to a bitter taste, suggesting they may share common brain wiring (Science, vol 323, p 1222). Other work has shown that judging a morally questionable act, such as theft, while smelling something disgusting leads to harsher moral judgements (Personality and Social Psychology Bulletin, vol 34, p 1096). What’s more, Allman points out that our language is loaded with analogies - we might find an experience “delicious”, say, or a person “nauseating”. This is no accident, he says.

Red herring

However, it is only in highly social animals that VENs live exclusively in the scent and taste regions. In the others, like giraffes and hippos, VENs seem to be sprinkled all over the brain. Allman, however, points out that these findings may be a red herring, since without understanding the genes they express, or their function, we can’t even be sure how closely these cells relate to human VENs. They may even be a different kind of cell that just looks similar.

Based on the evidence so far, however, Hof thinks that the ancestral VENs would have been more widespread, as seen in the hippo brain, and that over the course of evolution they then migrated to the ACC and FI in some animals, but not others - though he admits to having no idea why that might be. He suspects the pressures that shaped the primate brain may have been very different to those that drove the evolution of whales and dolphins.

Craig has hit upon one possibility that would seem to fit all of these big-brained animals. He points out that the bigger the brain, the more energy it takes to run, so it is crucial that it operates as efficiently as possible. A system that continually monitors the environment and the people or animals in it would therefore be an asset, allowing you to adapt quickly to a situation to save as much energy as possible. “Evolution produced an energy calculation system that incorporated not just the sensory inputs from the body but the sensory inputs from the brain,” Craig says. And the fact that we are constantly updating this picture of “how I feel now” has an interesting and very useful by-product: we have a concept that there is an “I” to do the feeling. “Evolution produced a very efficient moment-by-moment calculation of energy utilisation and that had an epiphenomenon, a by-product that provided a subjective representation of my feelings.”

If he’s right - and there is a long way to go before we can be sure - it raises a very humbling possibility: that far from being the pinnacle of brain evolution, consciousness might have been a big, and very successful accident.

This article has been edited since it was first posted

Caroline Williams is a writer based in Surrey, UK 

Issue 2874 of New Scientist magazine
The Not-So-Perfect Kilogram and Why the Metric System Might Be Screwed. By Judy Dutton

The world’s most perfect weight isn’t so perfect anymore. And that has scientists scared.

Image credit: International Bureau of Weights and Measures

Hidden in a vault outside Paris, vacuum-sealed under three bell jars, sits a palm-sized metal cylinder known as the International Prototype Kilogram, or “Le Grand K.” Forged in 1879 from an alloy of platinum and iridium, it was hailed as the “perfect” kilogram—the gold standard by which other kilograms would be judged.

Although it’s arguably the world’s most famous weight, Le Grand K doesn’t get out much. Since hydrocarbons on fingertips or moisture in the air could contaminate its pristine surface, it goes untouched for decades, under triple lock and key at the International Bureau of Weights and Measures. Every 40 years, however, it makes an appearance. The weight is ushered from its chamber, washed with alcohol, polished, and weighed against 80 official replicas hand-delivered from laboratories around the world. Today, whenever scientists need to verify something is precisely one kilogram, they turn to one of these replicas, over which Le Grand K reigns supreme.

This system sounds absurd, but not too long ago, lots of units relied on similar methods. The kilogram was just one of seven standards of measurement established by the French Academy of Sciences in 1791, all based on physical prototypes. These benchmarks caught on worldwide because standardization was sorely needed. At the time, some 250,000 different units of weights and measures existed in France alone, which meant that the only constant was complete chaos.

Weight Problem

While basing measurements on tangible benchmarks was an improvement, using physical standards wasn’t without its flaws. For one, they have a nasty habit of changing. In Le Grand K’s case, it’s been losing weight. At its most recent weigh-in in 1988, it was found to be 0.05 milligrams—about the weight of a grain of sand—lighter than its underling replicas. Experts aren’t sure where this weight went, but some theorize that the replicas have been handled more often, which could subtly add weight. Others postulate Le Grand K’s alloy is “outgassing,” which means air is gradually escaping the metal.

Whatever the reason for Le Grand K’s gradual wasting away, it’s got scientists scrambling for a more reliable standard. Some argue that this is long overdue, since all other units of measurement are already defined by fundamental constants of nature that can be reproduced anywhere anytime (provided you’ve got some sophisticated lab equipment). The meter, for example, used to be defined by a metal rod stored alongside Le Grand K. But in 1983, it was redefined as the distance light travels in a vacuum during 1/299,792,458 of a second.

Standardizing the kilogram has been trickier, though. Australian scientists are polishing a one-kilogram sphere of silicon, hoping that they’ll be able to count the number of atoms it contains to create a more accurate standard. American physicists at the National Institute of Standards and Technology (NIST) are attempting to redefine a kilogram in terms of the amount of voltage required to levitate a weight. But so far, neither approach can match Le Grand K’s accuracy.

Why should we care whether a kilogram in a vault is “perfect” or not? Because it’s bad news when your standard is no longer standardized. While no one’s worried whether a single kilogram of apples is a hair lighter or heavier at the produce stand, a small discrepancy can become a gargantuan one if you’re dealing with, say, a whole tanker of wheat. The kilogram is also used as a building block in other measurements. The joule, for instance, is the amount of energy required to move a one-kilogram weight one meter. The candela, a measure of the brightness of light, is measured in joules per second.

These links mean that if the kilogram is flawed, so are the joule and candela, which could eventually cause problems in an array of industries, particularly in technology. As microchips process more information at higher speeds, even tiny deviations will lead to catastrophes. Le Grand K’s unreliability “will start to be noticeable in the next decade or two in the electronics industry,” warns NIST physicist Richard Steiner. If your next smartphone is buggy, you’ll know which hunk of metal to blame.

So scientists continue to chase the perfect kilogram. “Maybe we have all been looking for too high-tech an answer,” says Stuart Davidson of England’s National Physical Laboratory. “There could be something really obvious out there we’ve missed.” The NPL’s website encourages others to give it a shot: Any better ideas on a postcard please. Until then, Le Grand K will remain king—short of true perfection, but as perfect as it gets.

This article appears in the July-August 2012 issue of mental_floss magazine.

Finding the Flotsam: Where Is Japan’s Floating Tsunami Wreckage Headed?

Scientists model where and when the detritus will reach the U.S. west coast

Image: NOAA, Rose Eveleth

When the 10-meter-high tsunami wave that followed the March 2011 magnitude 9.0 earthquake in Japan receded, it took with it some 23 million metric tons of material, including pieces of buildings, wood, plastics and more. Whereas most of the wreckage sank to the ocean floor, some of it is still floating toward other Pacific nations. The “debris field”—the visible wave of material—has dissipated, leaving the junk invisible to satellites.

So scientists at the National Oceanic and Atmospheric Administration (NOAA) and the University of Hawaii at Manoa (U.H.) who are monitoring that mass have modeled where it might go and when it might get there. You can see one of the scenarios, based on a model from the U.H.’s International Pacific Research Center Institute, in this video. For the model, scientists estimated that the tsunami left around 900,000 metric tons of floating debris in the ocean, although it is impossible to ever know the exact amount. Red areas highlight where the collection is densest, blue where it is least dense.

It is possible that most of that junk—which is not radioactive—will break up and sink before it gets to the U.S. west coast. And if it does, it will be almost impossible to tell whether it came from the tsunami, or from somewhere else, says Dianna Parker, who works with NOAA’s marine debris program. “We get debris from Asia all the time,’ she says, and even the most recent reports of buoys that many suspect came from the disaster could have come from elsewhere. “We’ve seen those kinds of buoys before the tsunami, too,” she adds.

Say No to Schistosoma!

Dear Tumbler Affectionado,

We are excited to announce that World Community Grid has launched a new project called;

Say No to Schistosoma!

Schistosomiasis is a tropical disease transmitted by freshwater snails. The disease kills 200,000 people each year and affects over 207 million people in 74 countries. Schistosomiasis is second only to malaria in its socioeconomic devastation, and to date, there are no available vaccines to prevent the disease. 

Researchers at the Inforium University in Belo Horizonte and FIOCRUZ-Minas, Brazil, are using World Community Grid to search for chemical compounds which may lead to new drugs for treating this terrible disease. 

Please join us and donate your unused computer time to aide in identifying potential drug candidates that could possibly be developed into treatments for schistosomiasis. 

To verify if you are contributing, or to start contributing, to this project, please click here

Thank you, 

The World Community Grid Team
Project Status and Findings:  
Information about this project is provided on the web pages below and by the project scientists on the Say No to Schistosoma website. If you have comments or questions about this project, please visit the Say No to Schistosoma forum.

 Mission
The mission of the Say No to Schistosoma project is to identify potential drug candidates that could possibly be developed into treatments for schistosomiasis. The extensive computing power of World Community Grid will be used to perform computer simulations of the interactions between millions of chemical compounds and certain target proteins. This will help find the most promising compounds that may lead to effective treatments for the disease. 

 Significance
Schistosomiasis is a tropical disease caused by parasitic worms that are transmitted by freshwater snails. The disease kills 200,000 people each year and affects over 207 million people. Schistosomiasis is second only to malaria in its socioeconomic devastation. Researchers at the Infórium University in Belo Horizonte and FIOCRUZ-Minas, Brazil, are using World Community Grid to search for chemical compounds which may lead to new drugs for treating the disease.

 Approach
A software program called VINA from The Scripps Research Institute in La Jolla, California, will be used to perform the virtual chemistry experiments. These virtual experiments will search to find which of millions of drug compounds might be able to disable particular proteins essential for the parasite’s survival. Screening for the best potential drug compounds is an early step in the process of developing effective treatments for the disease. With enough computing power, this screening can be done much more quickly than using conventional laboratory experiments. Existing computers available to the researchers would require approximately 30 years to perform the screening. However, it is estimated that the power of World Community Grid can reduce the time required to one year or less. Information about the best candidate compounds will be published by the scientists, and this information will be available in the public domain for other scientists to build upon with their research. Further laboratory work using the best candidates identified by this project could lead to the development of better drugs to fight schistosomiasis. 
30,000 Year-Old Plant

30,000 Year-Old Plants of the Day

Researchers at the Russian Academy of Science’s Soil Cryology Lab have managed to grow flowers using 30,000 year-old seeds preserved in the Russian permafrost.

The seeds of Silene stenophylla were buried by squirrels during the Upper Pleistocene, and covered with layers of frozen soil over thousands of years. Researchers eventually recovered them 125 feet below ground, still perfectly preserved at -7 degrees celsius.

The discovery makes S. stenophylla the oldest known plant species to be revived from ancient seeds, topping the 2,000 year-old “Phoenix palm” grown by Israeli scientists in 2008.

[discover]

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