The brain’s network switching stations for adaptive behavior

August 16th, 2013

I’m excited to announce that my latest scientific publication – “Multi-task connectivity reveals flexible hubs for adaptive task control” – was just published in Nature Neuroscience. The paper reports on a project I (along with my co-authors) have been working on for over a year. The goal was to use network science to better understand how human intelligence happens in the brain – specifically, our ability to rapidly adapt to new circumstances, as when learning to perform a task for the first time (e.g., how to use new technology).

The project built on our previous finding (from last year) showing that the amount of connectivity of a well-connected “hub” brain region in prefrontal cortex is linked to human intelligence. That study suggested (indirectly) that there may be hub regions that are flexible – capable of dynamically updating what brain regions they communicate with depending on the current goal.

Typical methods were not capable of more directly testing this hypothesis, however, so we took the latest functional connectivity approaches and pushed the limit, going well beyond the previous paper and what others have done in this area. The key innovation was to look at how functional connectivity changes across dozens of distinct task states (specifically, 64 tasks per participant). This allowed us to look for flexible hubs in the fronto-parietal brain network.

We found that this network contained regions that updated their global pattern of functional connectivity (i.e., inter-regional correlations) depending on which task was being performed.

In other words, the fronto-parietal network changed its brain-wide functional connectivity more than any other major brain network, and this updating appeared to code which task was being performed.

What’s the significance?

These results suggest a potential mechanism for adaptive cognitive abilities in humans:
Prefrontal and parietal cortices form a network with extensive connections projecting to other functionally specialized networks throughout the brain. Incoming instructions activate component representations – coded as neuronal ensembles with unique connectivity patterns – that produce a unique global connectivity pattern throughout the brain. Since these component representations are interchangeable it’s possible to implement combinations of instructions never seen before, allowing for rapid learning of new tasks from instructions.

Important points not mentioned or not emphasized in the journal article:

This study was highly hypothesis-driven, as it tested some predictions of our recent compositional theory of prefrontal cortex function (extended to include parietal cortex as well). That theory was first proposed earlier this year in Cole, Laurent, & Stocco (2013).

Also, as described in our online supplemental FAQ for the paper, we identified ‘adaptive task control’ flexible hubs, but there may be other kinds of flexible hubs in the brain. For instance, there may be flexible hubs for stable task control (maintaining task information via connectivity patterns over extended periods of time, only updating when necessary).

See our online supplemental FAQ for more important points that were not mentioned in the journal article. Additional information is also available from a press release from Washington University.

–MWCole

Having more global brain connectivity with some regions enhances intelligence

July 6th, 2012

A new study – titled “Global Connectivity of Prefrontal Cortex Predicts Cognitive Control and Intelligence” – was published just last week. In it, my co-authors and I describe our research showing that connectivity with a particular part of the prefrontal cortex can predict how intelligent someone is.

We measured intelligence using “fluid intelligence” tests, which measure your ability to solve novel visual puzzles. It turns out that scores on these tests correlate with important life outcomes like academic and job success. So, finding a neuroscientific factor underlying fluid intelligence might have some fairly important implications.

It turns out that it’s relatively unclear exactly what fluid intelligence tests actually test (what helps you solve novel puzzles, exactly?), so we also measured a more basic “cognitive control” ability thought to be related to fluid intelligence – working memory. This measures your ability to maintain and manipulate information in mind in a goal-directed manner.

Overall (i.e., global) brain connectivity with a part of left lateral prefrontal cortex (see figure above) could predict both fluid intelligence and cognitive control abilities.

What does this mean? One possibility is that this prefrontal region is a “flexible hub” that uses its extensive brain-wide connectivity to monitor and influence other brain regions in a goal-directed manner. This may sound a bit like it’s some kind of “homunculus” (little man) that single-handedly implements all brain functions, but in fact we’re suggesting it’s more like a feedback control system that is used often in engineering, that it only helps implement cognitive control (which supports fluid intelligence), and that it doesn’t do this alone.

Indeed, we found other independent factors that were important for predicting intelligence, suggesting there are several fundamental neural factors underlying intelligence. The global connectivity of this prefrontal region could account for 10% of the variability in fluid intelligence, while activity in this region accounts (independently) for 5% of the variability, and overall gray matter volume accounts (again independently) for an additional 6.7% of the variance. Together, these three factors accounted for 26% of the variance in fluid intelligence across individuals.

There are several important questions that this study raises. For instance, does this region change its connectivity depending on the task being performed, as the “flexible hub” hypothesis would suggest? Are there other regions whose global (or local) connectivity contributes substantially to intelligence and cognitive control abilities? Finally, what other factors are there in the brain that might be able to predict fluid intelligence across individuals?

-MC

The evolutionary importance of rapid instructed task learning (RITL)

January 23rd, 2011

We are rarely alone when learning something for the first time. We are social creatures, and whether it’s a new technology or an ancient tradition, we typically benefit from instruction when learning new tasks. This form of learning–in which a task is rapidly (within seconds) learned from instruction–can be referred to as rapid instructed task learning (RITL; pronounced “rittle”). Despite the fundamental role this kind of learning plays in our lives, it has been largely ignored by researchers until recently.

My Ph.D. dissertation investigated the evolutionary and neuroscientific basis of RITL.

RITL almost certainly played a tremendous role in shaping human evolution. The selective advantages of RITL for our species are clear: having RITL abilities allows us to partake in a giant web of knowledge shared with anyone willing to instruct us. We might have received instructions to avoid a dangerous animal we have never seen before (e.g., a large cat with a big mane), or instructions on how to make a spear and kill a lion with it. The possible scenarios in which RITL would have helped increase our chances of survival are virtually endless.

There are two basic forms of RITL. Read the rest of this entry »

Finding the most important brain regions

June 29th, 2010

When you type a search into Google it figures out the most important websites based in part on how many links each has from other websites. Taking up precious website space with a link is costly, making each additional link to a page a good indicator of importance.

We thought the same logic might apply to brain regions. Making a new brain connection (and keeping it) is metabolically and developmentally costly, suggesting that regions with many connections must be providing important enough functions to make those connections worth the sacrifice.

We developed two new metrics for quantifying the most connected—and therefore likely the most important—brain regions in a recently published study (Cole et al. (2010). Identifying the brain’s most globally connected regions, NeuroImage 49(4): 3132-3148).

We found that two large-scale brain networks were among the top 5% of globally connected regions using both metrics (see figure above). The cognitive control network (CCN) is involved in attention, working memory, decision-making and other important high-level cognitive processes (see Cole & Schneider, 2007). In contrast, the default-mode network (DMN) is typically anti-correlated with the CCN and is involved in mind-wandering, long-term memory retrieval, and self-reflection.

Needless to say, these networks have highly important roles! Without them we would have no sense of self-control (via the CCN) or even a sense of self to begin with (via the DMN).

However, there are other important functions (such as arousal, sleep regulation, breathing, etc.) that are not reflected here, most of which involve subcortical regions. These regions are known to project widely throughout the brain, so why aren’t they showing up?

It turns out that these subcortical regions only show up for one of the two metrics we used. This metric—unlike the other one—includes low-strength connections. Subcortical regions tend to be small and project weak connections all over the brain, such that only the metric including weak connections could identify them up.

I recently found out that this article received the 2010 NeuroImage Editor’s Choice Award (Methods section). I was somewhat surprised by this, since I thought there wasn’t much interest in the study. When I looked up the most popular articles at NeuroImage, however, I found out it was the 7th most downloaded article from January to May 2010. Hopefully this interest will lead to some innovative follow-ups to try to understand what makes these brain regions so special!

-MWCole

Cingulate Cortex and the Evolution of Human Uniqueness

November 12th, 2009

Figuring out how the brain decides between two options is difficult. This is especially true for the human brain, whose activity is typically accessible only via the small and occasionally distorted window provided by new imaging technologies (such as functional MRI (fMRI)).

In contrast, it is typically more accurate to observe monkey brains since the skull can be opened and brain activity recorded directly.

Despite this, if you were to look just at the human research, you would consider it a fact that the anterior cingulate cortex (ACC) increases its activity during response conflict. The thought is that this brain region detects that you are having trouble making decisions, and signals other brain regions to pay more attention.

If you were to only look at research with monkeys, however, you would think otherwise. No research with macaque monkeys (the ‘non-human primate’ typically used in neuroscience research) has found conflict activity in ACC.

My most recent publication looks at two possible explanations for this discrepancy: 1) Differences in methods used to study these two species, and 2) Fundamental evolutionary differences between the species.

Read the rest of this entry »

A Meta-Meta-Analysis of Brain Functions

October 17th, 2008

Thousands of brain imaging studies are published each year. A subset of these studies are replications, or slight variations, of previous studies. Attempting to come to a solid conclusion based on the complex brain activity patterns reported by all these replications can be daunting. Meta-analysis is one tool that has been used to make sense of it all.

Meta-analyses take locations of brain activity in published scientific papers and pool them together to see if there is any consistency.

This is typically done using a standardized brain that all the studies fit their data to (e.g., Talairach). Activation coordinates are then placed on a template brain as dots. When dots tend to clump together then the author can claim some consistency is present across studies. See the first figure for an example of this kind of result.

More sophisticated ways of doing this have emerged, however. One of these advanced methods is called activation likelihood estimation (ALE). This method was developed by Peter Terkeltaub et al. (in conjunction with Jason Chein and Julie Fiez) in 2002 and extended by Laird et al. in 2005.

ALE computes the probability of each part of the brain being active across studies. This is much more powerful than simple point-plotting because it takes much of the guess-work out of deciding if a result is consistent across studies or not.

Read the rest of this entry »

Keeping Up: Tips for Managing Science Reading

August 4th, 2008

Keeping up with new findings is constantly becoming more difficult with the rate of publication in just cognitive neuroscience increasing by over 200 per year, with an overall increase of 2333 over the last ten years  (see figure below). I will briefly describe some methods I’ve recently discovered to help deal with this onslaught of new information.

I have found that using a combination of computer applications and websites can be effective for keeping up with science readings.

The websites are useful for searching and subscribing to syndicated (RSS) feeds. The applications are useful for organizing articles.

Websites for searching

Google Scholar
This website is extremely useful for exploring a comprehensive collection of research on a particular topic. It uses Google’s legendary indexing algorithms to make keyword searching a breeze, while browsing citation links can reveal a chain of publications on a topic. It’s also useful because citations can be quickly imported into programs like EndNote, and articles that are often unavailable on other websites are made available via Google’s indexing.

Scopus
Scopus is “the largest abstract and citation database of research literature and quality web sources”. It’s very useful for seeing all the papers that have cited a particular article, and all the papers that article has cited. Google Scholar also has this feature, but in my experience there are more false-positives than with Scopus. The consistent link, citation, and abstract-viewing interface makes Scopus often more effective than Google Scholar. Read the rest of this entry »

Grand Challenges of Neuroscience: Day 6

July 21st, 2008

Topic 6: Causal Understanding


Causal understanding is an important part of human cognition.  How do we understand that a particular event or force has caused another event?  How do realize that inserting coins into a soda machine results in a cool beverage appearing below?  And ultimately, how do we understand people’s reactions to events?

The NSF workshop panel on the Grand Challenges of Mind and Brain highlighted the question of ‘causal understanding’ as their 6th research topic.   (This was the final topic in their report.)

In addition to studying causal understanding, it is probably just as important to study causal misunderstanding: that is, why do individuals infer the wrong causes for events?  Or incorrect results from causes? Studying the errors we make in causal inference and understanding may help us discover the underlying neural mechanisms.  

It probably isn’t too difficult to imagine that progress on causal understanding, and improvements in our ability to be correct about causation, will probably be important for the well-being of humanity.  But what kinds of experiments and methods could be used to human brain mechanisms of  causal understanding?

Read the rest of this entry »

A Brief Introduction to Reinforcement Learning

June 2nd, 2008

Computational models that are implemented, i.e., written out as equations or software, are an increasingly important tool for the cognitive neuroscientist.  This is because implemented models are, effectively, hypotheses that have been worked out to the point where they make quantitative predictions about behavior and/or neural activity.

In earlier posts, we outlined two computational models of learning hypothesized to occur in various parts of the brain, i.e., Hebbian-like LTP (here and here) and error-correction learning (here and here). The computational model described in this post contains hypotheses about how we learn to make choices based on reward.

The goal of this post is to introduce a third type of learning: Reinforcement Learning (RL).  RL is hypothesized by a number of cognitive neuroscientists to be implemented by the basal ganglia/dopamine system.  It has become somewhat of a hot topic in Cognitive Neuroscience and received a lot of coverage at this past year’s Computational Cognitive Neuroscience Conference. Read the rest of this entry »

Levels of Analysis and Emergence: The Neural Basis of Memory

May 30th, 2008

A square 'emerges' from its surroundings (at least in our visual system)Cognitive neuroscience constantly works to find the appropriate level of description (or, in the case of computational modeling, implementation) for the topic being studied.  The goal of this post is to elaborate on this point a bit and then illustrate it with an interesting recent example from neurophysiology.

As neuroscientists, we can often  choose to talk about the brain at any of a number of levels: atoms/molecules, ion channels and other proteins, cell compartments, neurons, networks, columns, modules, systems, dynamic equations, and algorithms.

However, a description at too low a level might be too detailed, causing one to lose the forest for the trees.  Alternatively, a description at too high a level might miss valuable information and is less likely to generalize to different situations.

For example, one might theorize that cars work by propelling gases from their exhaust pipes.  Although this might be consistent with all of the observed data, by looking “under the hood” one would find evidence that this model of a car’s function is incorrect.

Read the rest of this entry »

CNS Meeting 2008: Development of Cognitive Control

April 19th, 2008

I just got back from CNS a few days ago. I thought I’d write a quick summary of one of the more interesting symposia at the conference.

Taking place Monday (4/14) afternoon, The rise and fall of cognitive control: Lifespan development covered how executive brain functions develop and peak in the 20s and 30s, falling again toward the end of life.

The first talk, by Cindy Lustig, reported on a functional MRI study of 239 individuals ranging from 9 to 97 years of age. She found that the “default-network” brain activity (likely related to mind wandering) was better suppressed during difficult tasks early in life and decreased later in life. This suggests that difficulties older people have with hard tasks may originate in their poor ability to reduce background thoughts.

Adele Diamond gave the next talk, which focused on an impressive preschool program that improves cognitive control in children to help them with future school success. The program, called Tools of the Mind, is based on research showing that self-regulation (i.e., cognitive control) is very predictive of future academic success. The program successfully integrates with the children’s play, and Dr. Diamond’s research shows convincingly that it is able to improve cognitive control and subsequent school success. The above photo is of two children “playing” the program’s ‘Buddy Reading’ task, which promotes inhibition of inappropriate impulses using a reminder icon held by the child in the role of listener (on the right in the above photo).

The final talk, by Bradley Schlaggar of Washington University at St. Louis, described tracking changes in resting state connectivity with development. As presented by Steven Petersen at HBM 2007, Dr. Schlaggar showed how dorsal anterior cingulate changes its membership in networks over time. The idea of showing how regional membership in global networks can change with development is very exciting and will certainly lead to future insights into human developmental processes.

-MWCole

Joaquin Fuster on Cortical Dynamics

April 5th, 2008

I recently watched this talk (below) by Joaquin Fuster. His theories provide a good integration of cortical functions and distributed processing in working and long-term memory. He also has some cool videos of likely network interactions across cortex (in real time) in his talk.

Here is a diagram of Dr. Fuster’s view of cortical hierarchies:

Joaquin Fuster’s talk:

Link to Joaquin Fuster’s talk [Google Video]

Here is an excerpt from Dr. Fuster’s amazing biography:
Read the rest of this entry »

Combining Simple Recurrent Networks and Eye-Movements to study Language Processing

April 5th, 2008

BBS image of GLENMORE model

Modern technologies allow eye movements to be used as a tool for studying language processing during tasks such as natural reading. Saccadic eye movements during reading turn out to be highly sensitive to a number of linguistic variables. A number of computational models of eye movement control have been developed to explain how these variables affect eye movements. Although these models have focused on relatively low-level cognitive, perceptual and motor variables, there has been a concerted effort in the past few years (spurred by psycholinguists) to extend these computational models to syntactic processing.

During a modeling symposium at ECEM2007 (the 14th European Conference on Eye Movements), Dr. Ronan Reilly presented a first attempt to take syntax into account in his eye-movement control model (GLENMORE; Reilly & Radach, Cognitive Systems Research, 2006). Read the rest of this entry »

Measuring Innate Functional Brain Connectivity

March 29th, 2008

 Functional magnetic resonance imaging (fMRI), a method for safely measuring brain activity, has been around for about 15 years. Within the last 10 of those years a revolutionary, if mysterious, method has been developing using the technology. This method, resting state functional connectivity (rs-fcMRI), has recently gained popularity for its putative ability to measure how brain regions interact innately (outside of any particular task context).

Being able to measuring innate functional brain connectivity would allow us to know if a set of regions active during a particular task is, in fact, well connected enough generally to be considered a network. We could then predict what brain regions are likely to be active together in the future. This could, in turn, motivate us to look deeper at the nature of each brain region and how it contributes to the neuronal networks underlying our behavior.

Rs-fcMRI uses correlations of very slow fluctuations in fMRI signals (< 0.1 Hz) when participants are at rest to determine how regions are connected. The origin of these slow fluctuations has been unclear.

Some have argued that the thoughts and day dreams of participants “at rest” may explain the strong correlations typically found between brain regions. Recently, Vincent et al., 2007 sought to address this possibility using fMRI with anesthetized monkeys.

The idea is that if unconscious monkey brains show low-frequency correlated activity across known brain networks, then such findings in humans at conscious rest are likely not due to spurious thoughts, but something more innate. Read the rest of this entry »

The Will to be Free, Part II

November 6th, 2007

 Several months ago I posted The Will to be Free, Part I. In that post I explained that memory is the key to free will. However, this insight isn’t quite satisfactory. We need three additional things to complete the picture: the ability to choose based on predictions, internal desires, and self-awareness. (A quick disclaimer: These ideas are all extremely speculative. I’ll probably test most of them at some point, but right now I’m just putting them out there to hopefully allow for refinement of these hypotheses.) First, the ability to choose based on predictions. As mentioned last time, free will comes down to decision making. Specifically it comes down to our ability to make a decision based on internal sources (or at least condoned by them), rather than external coercive forces. If we cannot predict the outcome of our decision with any certainty, then decision making is pointless. For instance, if no matter what I choose to order at dinner a random dish is served then I had no freedom to choose in the first place. Thus, our ability to predict is necessary for free will. What are these “internal sources” involved in decision making that I mentioned earlier? They are the second new idea needed to complete our picture of free will: desires. Read the rest of this entry »