Non-Invasive Brain-to-Brain Interface (BBI): Establishing Functional Links between Two Brains
Transcranial focused ultrasound (FUS) is capable of modulating the neural activity of specific brain regions, with a potential role as a non-invasive computer-to-brain interface (CBI). In conjunction with the use of brain-to-computer interface (BCI) techniques that translate brain function to generate computer commands, we investigated the feasibility of using the FUS-based CBI to non-invasively establish a functional link between the brains of different species (i.e. human and Sprague-Dawley rat), thus creating a brain-to-brain interface (BBI). The implementation was aimed to non-invasively translate the human volunteer’s intention to stimulate a rat’s brain motor area that is responsible for the tail movement. The volunteer initiated the intention by looking at a strobe light flicker on a computer display, and the degree of synchronization in the electroencephalographic steady-state-visual-evoked-potentials (SSVEP) with respect to the strobe frequency was analyzed using a computer. Increased signal amplitude in the SSVEP, indicating the volunteer’s intention, triggered the delivery of a burst-mode FUS (350 kHz ultrasound frequency, tone burst duration of 0.5 ms, pulse repetition frequency of 1 kHz, given for 300 msec duration) to excite the motor area of an anesthetized rat transcranially. The successful excitation subsequently elicited the tail movement, which was detected by a motion sensor. The interface was achieved at 94.0±3.0% accuracy, with a time delay of 1.59±1.07 sec from the thought-initiation to the creation of the tail movement. Our results demonstrate the feasibility of a computer-mediated BBI that links central neural functions between two biological entities, which may confer unexplored opportunities in the study of neuroscience with potential implications for therapeutic applications.
The Power of Swarms Can Help Us Fight Cancer, Understand the Brain, and Predict the Future
A flock of red-winged blackbirds forms and re-forms over California’s Sacramento Valley.
The first thing to hit Iain Couzin when he walked into the Oxford lab where he kept his locusts was the smell, like a stale barn full of old hay. The second, third, and fourth things to hit him were locusts. The insects frequently escaped their cages and careened into the faces of scientists and lab techs. The room was hot and humid, and the constant commotion of 20,000 bugs produced a miasma of aerosolized insect exoskeleton. Many of the staff had to wear respirators to avoid developing severe allergies. “It wasn’t the easiest place to do science,” Couzin says.In the mid-2000s that lab was, however, one of the only places on earth to do the kind of science Couzin wanted. He didn’t care about locusts, per se—Couzin studies collective behavior. That’s swarms, flocks, schools, colonies … anywhere the actions of individuals turn into the behaviors of a group. Biologists had already teased apart the anatomy of locusts in detail, describing their transition from wingless green loners at birth to flying black-and-yellow adults. But you could dissect one after another and still never figure out why they blacken the sky in mile-wide plagues. Few people had looked at how locusts swarm since the 1960s—it was, frankly, too hard. So no one knew how a small, chaotic group of stupid insects turned into a cloud of millions, united in one purpose.
Couzin would put groups of up to 120 juveniles into a sombrero-shaped arena he called the locust accelerator, letting them walk in circles around the rim for eight hours a day while an overhead camera filmed their movements and software mapped their positions and orientations. He eventually saw what he was looking for: At a certain density, the bugs would shift to cohesive, aligned clusters. And at a second critical point, the clusters would become a single marching army. Haphazard milling became rank-and-file—a prelude to their transformation into black-and-yellow adults.
That’s what happens in nature, but no one had ever induced these shifts in the lab—at least not in animals. In 1995 a Hungarian physicist named Tamás Vicsek and his colleagues devised a model to explain group behavior with a simple—almost rudimentary—condition: Every individual moving at a constant velocity matches its direction to that of its neighbors within a certain radius. As this hypothetical collective becomes bigger, it flips from a disordered throng to an organized swarm, just like Couzin’s locusts. It’s a phase transition, like water turning to ice. The individuals have no plan. They obey no instructions. But with the right if-then rules, order emerges.
Couzin wanted to know what if-then rules produced similar behaviors in living things. “We thought that maybe by being close to each other, they could transfer information,” Couzin says. But they weren’t communicating in a recognizable way. Some other dynamic had to be at work.
Rules that produce majestic cohesion out of local jostling turn up everywhere.
The answer turned out to be quite grisly. Every morning, Couzin would count the number of locusts he placed in the accelerator. In the evening, his colleague Jerome Buhl would count them as he took them out. But Buhl was finding fewer individuals than Couzin said he had started with. “I thought I was going mad,” Couzin says. “My credibility was at stake if I couldn’t even count the right number of locusts.”When he replayed the video footage and zoomed in, he saw that the locusts were biting each other if they got too close. Some unlucky individuals were completely devoured. That was the key. Cannibalism, not cooperation, was aligning the swarm. Couzin figured out an elegant proof for the theory: “You can cut the nerve in their abdomen that lets them feel bites from behind, and you completely remove their capacity to swarm,” he says.
Couzin’s findings are an example of a phenomenon that has captured the imagination of researchers around the world. For more than a century people have tried to understand how individuals become unified groups. The hints were tantalizing—animals spontaneously generate the same formations that physicists observe in statistical models. There had to be underlying commonalities. The secrets of the swarm hinted at a whole new way of looking at the world.
But those secrets were hidden for decades. Science, in general, is a lot better at breaking complex things into tiny parts than it is at figuring out how tiny parts turn into complex things. When it came to figuring out collectives, nobody had the methods or the math.
Now, thanks to new observation technologies, powerful software, and statistical methods, the mechanics of collectives are being revealed. Indeed, enough physicists, biologists, and engineers have gotten involved that the science itself seems to be hitting a density-dependent shift. Without obvious leaders or an overarching plan, this collective of the collective-obsessed is finding that the rules that produce majestic cohesion out of local jostling turn up in everything from neurons to human beings. Behavior that seems impossibly complex can have disarmingly simple foundations. And the rules may explain everything from how cancer spreads to how the brain works and how armadas of robot-driven cars might someday navigate highways. The way individuals work together may actually be more important than the way they work alone.
Photo: Lukas Felzmann
First mind-reading implant
gives rats telepathic power
I, for one, welcome our new, telepathic, rat overlords.
Neuroprosthesis gives rats the ability to ‘touch’ infrared light
Researchers have given rats the ability to “touch” infrared light, normally invisible to them, by fitting them with an infrared detector wired to microscopic electrodes implanted in the part of the mammalian brain that processes tactile information. The achievement represents the first time a brain-machine interface has augmented a sense in adult animals, said Duke University neurobiologist Miguel Nicolelis, who led the research team.
The experiment also demonstrated for the first time that a novel sensory input could be processed by a cortical region specialized in another sense without “hijacking” the function of this brain area said Nicolelis. This discovery suggests, for example, that a person whose visual cortex was damaged could regain sight through a neuroprosthesis implanted in another cortical region, he said.
Although the initial experiments tested only whether rats could detect infrared light, there seems no reason that these animals in the future could not be given full-fledged infrared vision, said Nicolelis. For that matter, cortical neuroprostheses could be developed to give animals or humans the ability to see in any region of the electromagnetic spectrum, or even magnetic fields. “We could create devices sensitive to any physical energy,” he said. “It could be magnetic fields, radio waves, or ultrasound. We chose infrared initially because it didn’t interfere with our electrophysiological recordings.”
Nicolelis and colleagues Eric Thomson and Rafael Carra published their findings February 12, 2013 in the online journal Nature Communications. Their research was sponsored by the National Institute of Mental Health.
