The Ricky Gervais Show on the "I-Illusion"

Thanks to my son Jon for pointing me to this humorous video.

Neural correlates of religious belief - neuroscience and spirituality

I'm realizing that I have a sufficient number of notes from this area in my queue that I'm not going to get to them separately. So, here I pass on first some links to recent publications and then some work on neural correlates of religious belief.

First, three publications:

"How God changes your brain"

"Contemplative Science: Where Buddhism and Neuroscience Converge"

A conference on Neuroscience and spiritual practices

Next,
Kapogiannis and collaborators attempt to model the complexity of religious belief and then provide brain imaging data correlate their categories with well known brain networks:

We propose an integrative cognitive neuroscience framework for understanding the cognitive and neural foundations of religious belief. Our analysis reveals 3 principle psychological dimensions of religious belief (God's perceived level of involvement, God's perceived emotion, and doctrinal/experiential religious knowledge), which functional MRI localizes within networks processing Theory of Mind regarding intent and emotion, abstract semantics, and imagery. Our results are unique in demonstrating that specific components of religious belief are mediated by well-known brain networks, and support contemporary psychological theories that ground religious belief within evolutionary adaptive cognitive functions.

In a less ambitious effort, Inzlicht et al. suggest that religious people are more chilled out when they commit errors, reflected by reduced reactivity of their anterior cingulate cortex:

Many people derive peace of mind and purpose in life from their belief in God. For others, however, religion provides unsatisfying answers. Are there brain differences between believers and nonbelievers? Here we show that religious conviction is marked by reduced reactivity in the anterior cingulate cortex (ACC), a cortical system that is involved in the experience of anxiety and is important for self-regulation. In two studies, we recorded electroencephalographic neural reactivity in the ACC as participants completed a Stroop task. Results showed that stronger religious zeal and greater belief in God were associated with less firing of the ACC in response to error and with commission of fewer errors. These correlations remained strong even after we controlled for personality and cognitive ability. These results suggest that religious conviction provides a framework for understanding and acting within one's environment, thereby acting as a buffer against anxiety and minimizing the experience of error.

To be less helpful to others, watch violent media...

A sobering study from Bushman and Anderson:

Two studies tested the hypothesis that exposure to violent media reduces aid offered to people in pain. In the first study, participants played a violent or nonviolent video game for 20 min. After game play, while completing a lengthy questionnaire, they heard a loud fight, in which one person was injured, outside the lab. Participants who played violent games took longer to help the injured victim, rated the fight as less serious, and were less likely to "hear" the fight in comparison to participants who played nonviolent games. In the second study, violent- and nonviolent-movie attendees witnessed a young woman with an injured ankle struggle to pick up her crutches outside the theater either before or after the movie. Participants who had just watched a violent movie took longer to help than participants in the other three conditions. The findings from both studies suggest that violent media make people numb to the pain and suffering of others.

How to enhance the wisdom of one...

The point of James Surowiecki's engaging book, "The Wisdom of Crowds" is that a marketplace - of ideas, goods, services, whatever - can make astonishingly accurate predictions of election outcomes, Oscar winners, etc. Herzog and Hertwig ask how a single individual might improve a best guess for an outcome and test a Hegelian process they call "dialectical bootstrapping." After making the first estimate, consider the reasons and assumptions underpinning that estimate (and how they might be off target), and then formulate a new, second estimate that harks back to somewhat different knowledge.

They tested the efficacy of this method by asking 101 students at the University of Basel to date a collection of 40 historical events (e.g., the discovery of electricity), 10 each from the 16th, 17th, 18th, and 19th centuries. Each participant was randomly assigned to one of two conditions. In both conditions, participants first generated their estimates without knowing that they would be asked later to generate a second estimate. In the dialectical-bootstrapping condition, participants (n= 50) were then asked to give dialectical estimates (while their first estimates were displayed in front of them) using a technique inspired by the consider-the-opposite strategy: First, assume that your first estimate is off the mark. Second, think about a few reasons why that could be. Which assumptions and considerations could have been wrong? Third, what do these new considerations imply? Was the first estimate rather too high or too low? Fourth, based on this new perspective, make a second, alternative estimate.

They found that the improvement in accuracy (in years) over the first estimate was twice as large for the dialectical average than for the repeat average, although averaging the first estimates from two random individuals worked better still.

Roots of our social glue

Angier does a nice summary of ideas in Hrdy's forthcoming new book “Mothers and Others: The Evolutionary Origins of Mutual Understanding,” (Harvard Univ. Press):

...the extraordinary social skills of an infant are at the heart of what makes us human. Through its ability to solicit and secure the attentive care not just of its mother but of many others in its sensory purview, a baby promotes many of the behaviors and emotions that we prize in ourselves and that often distinguish us from other animals, including a willingness to share, to cooperate with strangers, to relax one’s guard...Our capacity to cooperate in groups, to empathize with others and to wonder what others are thinking and feeling...probably arose in response to the selective pressures of being in a cooperatively breeding social group, and the need to trust and rely on others and be deemed trustworthy and reliable in turn. Babies became adorable and keen to make connections with every passing adult gaze....mother chimpanzees and gorillas jealously hold on to their infants for the first six months or more of life. Other females may express real interest in the newborn, but the mother does not let go: you never know when one of those females will turn infanticidal, or be unwilling or unable to defend the young ape against an infanticidal male.

Dr. Hrdy wrote her book in part to counter what she sees as the reigning dogma among evolutionary scholars that humans evolved their extreme sociality and cooperative behavior to better compete with other humans. “I’m not comfortable accepting this idea that the origins of hypersociality can be found in warfare, or that in-group amity arose in the interest of out-group enmity,” she said in a telephone interview. Sure, humans have been notably violent and militaristic for the last 12,000 or so years, she said, when hunter-gatherers started settling down and defending territories, and populations started getting seriously dense. But before then? There weren’t enough people around to wage wars. By the latest estimates, the average population size during the hundreds of thousands of years of human evolution that preceded the Neolithic Age may have been around 2,000 breeding adults. “What would humans have been fighting over?” Dr. Hrdy said. “They were too busy trying to keep themselves and their children alive.”

Dr. Hrdy also argues that our human ancestors became emotionally modern long before the human brain had reached its current average volume of 1,300 cubic centimeters, which is about three times the size of a chimpanzee brain — in other words, that we became the nicest apes before becoming the smartest. You don’t need a bulging brain to evolve cooperative breeding. Many species of birds breed cooperatively, as do lions, rats, meerkats, wolves and marmosets, among others. But to become a cooperatively breeding ape, and to persuade a bunch of smart, hot-tempered, suspicious, politically cunning primates to start sharing child care and provisionings, now that took a novel evolutionary development, the advent of this thing called trust.

The Myth of Language Universals

To continue the thread from several previous posts, I pass on the abstract of a draft article by Evans and Levinson titled "The Myth of Language Universals: Language diversity and its importance for cognitive science" :

Talk of linguistic universals has given cognitive scientists the impression that languages are all built to a common pattern. In fact, there are vanishingly few universals of language in the direct sense that all languages exhibit them. Instead, diversity can be found at almost every level of linguistic organization. This fundamentally changes the object of enquiry from a cognitive science perspective.

The article summarizes decades of cross-linguistic work by typologists and descriptive linguists, showing just how few and unprofound the universal characteristics of language are, once we honestly confront the diversity offered to us by the world's 6-8000 languages. After surveying the various uses of 'universal', we illustrate the ways languages vary radically in sound, meaning, and syntactic organization, then examine in more detail the core grammatical machinery of recursion, constituency, and grammatical relations. While there are significant recurrent patterns in organization, these are better explained as stable engineering solutions satisfying multiple design constraints,reflecting both cultural-historical factors and the constraints of human cognition.

Linguistic diversity then becomes the crucial datum for cognitive science: we are the only species with a communication system which is fundamentally variable at all levels. Recognising the true extent of structural diversity in human language opens up exciting new research directions for cognitive scientists, offering thousands of different natural experiments given by different languages, with new opportunities for dialogue with biological paradigms concerned with change and diversity, and confronting us with the extraordinary plasticity of the highest human skills.

MindBlog's winter office...

Inspired by 'the view from your window' feature of Andrew Sullivan's Blog, I thought I would post an iPhone photo of where I am sitting (in Fort Lauderdale, Florida) as I bang out MindBlog's posts. I will be heading back to Madison Wisconsin in early April.

How to keep from stumbling on steps...

Elliott et al. make the neat observation that a simple visual illusion can lead to safer stepping behavior. The perceived height of a step is manipulated as shown in this figure:

Subjects perceived the step to be higher in the V (vertical stripes on the height dimension) configuration on the right compared to the H (horizontal stripes) configuration on the left, and correspondingly raised their toes higher to clear the step.

Neuroscience and the soul.

A recent letter from Martha Farah to Science Magazine is worth passing on:

Science and religion have had a long relationship, by turns collegial and adversarial. In the 17th century Galileo ran afoul of the Church's geocentrism, and in the 19th century Darwin challenged the biblical account of creation. The breaches that open at such times often close again, as religions determine that the doctrine in question is not an essential part of faith. This is precisely what happened with geocentrism and, outside of certain American fundamentalist Christian sects, evolution.

A new challenge to the science-religion relationship is currently at hand. We hope that, with careful consideration by scientists and theologians, it will not become the latest front in what some have called the "culture war" between science and religion. The challenge comes from neuroscience and concerns our understanding of human nature.

Most religions endorse the idea of a soul (or spirit) that is distinct from the physical body. Yet as neuroscience advances, it increasingly seems that all aspects of a person can be explained by the functioning of a material system. This first became clear in the realms of motor control and perception. Yet, models of perceptual and motor capacities such as color vision and gait do not directly threaten the idea of the soul. You can still believe in what Gilbert Ryle called "the ghost in the machine" and simply conclude that color vision and gait are features of the machine rather than the ghost.

However, as neuroscience begins to reveal the mechanisms underlying personality, love, morality, and spirituality, the idea of a ghost in the machine becomes strained. Brain imaging indicates that all of these traits have physical correlates in brain function. Furthermore, pharmacologic influences on these traits, as well as the effects of localized stimulation or damage, demonstrate that the brain processes in question are not mere correlates but are the physical bases of these central aspects of our personhood. If these aspects of the person are all features of the machine, why have a ghost at all?

By raising questions like this, it seems likely that neuroscience will pose a far more fundamental challenge than evolutionary biology to many religions. Predictably, then, some theologians and even neuroscientists are resisting the implications of modern cognitive and affective neuroscience. "Nonmaterialist neuroscience" has joined "intelligent design" as an alternative interpretation of scientific data. This work is counterproductive, however, in that it ignores what most scholars of the Hebrew and Christian scriptures now understand about biblical views of human nature. These views were physicalist, and body-soul dualism entered Christian thought around a century after Jesus' day.

To be sure, dualism is intuitively compelling. Yet science often requires us to reject otherwise plausible beliefs in the face of evidence to the contrary. A full understanding of why Earth orbits the Sun (as a consequence of the way the solar system was formed) took another century after Galileo's time to develop. It may take even longer to understand why certain material systems give rise to consciousness. In the meantime, just as Galileo's view of Earth in the heavens did not render our world any less precious or beautiful, neither does the physicalism of neuroscience detract from the value or meaning of human life.

Saving the world...

A University of Vermont course in the spring of 2008 came up with a magnum opus now published in the Proceedings of the National Academy titled "Overcoming systemic roadblocks to sustainability: The evolutionary redesign of worldviews, institutions, and technologies." I totally have a mind-numbing headache from reading this ponderous but worthwhile effort, and give you a few clips from their summary of "an integrated set of worldviews, institutions, and technologies to stimulate and seed evolutionary redesign of the current socio-ecological regime to achieve global sustainability":

Redefine Well-Being Metrics.
In any new context, we first have to remember that the goal of an economy is to sustainably improve human well-being and quality of life. Material consumption and GDP are merely means to that end, not ends in themselves. We have to recognize, as both ancient wisdom and new psychological research tell us, that material consumption beyond real need can actually reduce overall well-being.
Ensure the Well-Being of Populations During the Transition.
We must ensure that reductions in economic output and consumption fall on those with the lowest marginal utility of consumption, the wealthy. Presently, the U.S. tax code taxes the third wealthiest man in the world, Warren Buffett, at 17.7%, while his receptionist is taxed at the average rate of 30%....although qualitative development may continue indefinitely... existing levels of physical economic output and consumption are already unsustainable and should be reduced.
Reduce Complexity and Increase Resilience.
Efforts to create new cultural/institutional variants can benefit from the lessons offered by history, particularly cases of successful adaptation...Although environmental factors contribute to decline, equally important are the decisions made during the crises. A society's responses depend on the ability of its political, economic, and social institutions to respond, as well as on its cultural values.
Expand the “Commons Sector.”
Recognizing that we are in a biophysical crisis because of our over-consumption and lack of protection of ecosystem services, we must invest in institutions and the technologies required to reduce the impact of the market economy and to preserve and protect public goods. It is now time to create another major category of institution, the commons sector, which would be responsible for managing existing common assets and for creating new ones. Some assets should be held in common because it is more just; these include resources created by nature or by society as a whole.
Remove Barriers to Improving Knowledge and Technology.
With the invention of television, political advertisements became a critical outlet for candidates to broadcast their message and to sway voters. However, the decentralized nature of the Internet allows citizens to gain knowledge about what is done in their name, just as politicians can find out more about those they claim to represent. As a means of two-way communication, the Internet provides voters the ability to speak out within their government without leaving their homes. For the Internet to transform the idea of electronic democracy, universal access is critical. Currently technological, financial, and social barriers exist to such universal accessibility. Removal of these barriers thus becomes a major goal for replacement of the current plutocracy with real democracy.

Persistent effect of early abuse or deprivation on immune function in humans.

The wisconsin group that has studied various aspect of early abuse and deprivation in children offers evidence that adult immune function is compromised in these children, even if they were adopted into nuturing families and more benevolent settings.

It is well known that children need solicitous parenting and a nurturing rearing environment to ensure their normal behavioral development. Early adversity often negatively impacts emotional and mental well-being, but it is less clearly established how much the maturation and regulation of physiological systems is also compromised. The following research investigated the effect of 2 different types of adverse childhood experiences, early deprivation through institutionalization and physical abuse, on a previously unexplored outcome: the containment of herpes simplex virus (HSV). The presence of HSV-specific antibody in salivary specimens was determined in 155 adolescents, including 41 postinstitutionalized, 34 physically-abused, and 80 demographically-similar control youth. Across 4 school and home days, HSV antibody was higher in both postinstitutionalized and physically-abused adolescents when compared with control participants. Because the prevalence of HSV infection was similar across the groups, the elevated antibody was likely indicative of viral recrudescence from latency. Total secretory Ig-A secretion was associated with HSV, but did not account for the group differences in HSV-specific antibody. These findings are likely caused by a failure of cellular immune processes to limit viral reactivation, indicating a persistent effect of early rearing on immune functioning. The fact that antibody profiles were still altered years after adoption into a more benevolent setting with supportive families suggests these results were not caused by contemporaneous factors, but rather reflect a lingering influence of earlier life experiences.

From oral to moral

An interesting synthesis from Chapman et al.

In common parlance, moral transgressions "leave a bad taste in the mouth." This metaphor implies a link between moral disgust and more primitive forms of disgust related to toxicity and disease, yet convincing evidence for this relationship is still lacking. We tested directly the primitive oral origins of moral disgust by searching for similarity in the facial motor activity evoked by gustatory distaste (elicited by unpleasant tastes), basic disgust (elicited by photographs of contaminants), and moral disgust (elicited by unfair treatment in an economic game). We found that all three states evoked activation of the levator labii muscle region of the face, characteristic of an oralnasal rejection response. These results suggest that immorality elicits the same disgust as disease vectors and bad tastes.

A summary graphic from the review of this work by Rozin et al. and some of their comments:

Domains of disgust. The schematic represents routes by which eliciting situations may trigger the disgust output program. Those that run through the disgust evaluation system--which includes appraisal of the elicitor, feelings, and contamination ideation--trigger the full disgust emotion. Solid lines represent routes through which an elicitor can activate the disgust evaluation-output program. Dashed lines (green) represent direct elicitation of the disgust output program. The dotted line (brown) represents a metaphoric, indirect route.

According to the principle of preadaptation, a system that evolves for one purpose is later used for another purpose. From this viewpoint, disgust originates in the mammalian bitter taste rejection system, which directly activates a disgust output system. This primal route (e.g., bitter and some other tastes) evokes only the output program, without a disgust evaluation phase. During human evolution, the disgust output system was harnessed to a disgust evaluation system that responded not to simple sensory inputs (such as bitter tastes) but to more cognitively elaborated appraisals (e.g., a cockroach). Initially, the evaluation system was a food rejection system that rejected potential foods on the basis of their nature or perceived origin. This was the first "true disgust," because it engaged this evaluation system. Later, through some combination of biological and cultural evolution, the eliciting category was enlarged to include reminders of our animal nature, as wel as some people or social groups. This process had adaptive value, because by making things or thoughts disgusting a culture could communicate their negativity and cause withdrawal from them.

Brain activity started by music you think you are going to hear.

Here is an interesting piece of work from Leaver et al:

Music consists of sound sequences that require integration over time. As we become familiar with music, associations between notes, melodies, and entire symphonic movements become stronger and more complex. These associations can become so tight that, for example, hearing the end of one album track can elicit a robust image of the upcoming track while anticipating it in total silence. Here, we study this predictive "anticipatory imagery" at various stages throughout learning and investigate activity changes in corresponding neural structures using functional magnetic resonance imaging. Anticipatory imagery (in silence) for highly familiar naturalistic music was accompanied by pronounced activity in rostral prefrontal cortex (PFC) and premotor areas. Examining changes in the neural bases of anticipatory imagery during two stages of learning conditional associations between simple melodies, however, demonstrates the importance of fronto-striatal connections, consistent with a role of the basal ganglia in "training" frontal cortex. Another striking change in neural resources during learning was a shift between caudal PFC earlier to rostral PFC later in learning. Our findings regarding musical anticipation and sound sequence learning are highly compatible with studies of motor sequence learning, suggesting common predictive mechanisms in both domains.

A mother's experience can alter her offspring's memory performance.

Here are some fascinating experiments, done in mice to be sure (but likely to be shown for humans soon, as with so many other mouse models). It is known that exposure to an enriched environment enhances learning and memory in mice [which is reflected by an enhancement of nerve-nerve signaling in the hippocampus termed long term potentiation (LTP)]. This new study shows that these effects can be transmitted to the next generation; the authors observed that LTP was enhanced in the offspring of enriched mothers. Moreover, the characteristic defects in LTP and contextual fear conditioning of ras–Gfr-knockout mice were masked in the offspring of knockout mice exposed to an enriched environment. These data raise the intriguing possibility that a mother's experience can induce epigenetic changes that influence her offspring's memory performance (see Tuesday's post for information on another maternal effect and information on epigenetic effects). If a similar phenomenon occurs in humans, the effectiveness of one's memory during adolescence, particularly in those with defective cell signaling mechanisms that control memory, can be influenced by environmental stimulation experienced by one's mother during her youth. A portion of the abstract:

The idea that qualities acquired from experience can be transmitted to future offspring has long been considered incompatible with current understanding of genetics. However, the recent documentation of non-Mendelian transgenerational inheritance makes such a "Lamarckian"-like phenomenon more plausible. Here, we demonstrate that exposure of 15-d-old mice to 2 weeks of an enriched environment (EE), that includes exposure to novel objects, elevated social interactions and voluntary exercise, enhances long-term potentiation (LTP) not only in these enriched mice but also in their future offspring through early adolescence, even if the offspring never experience EE. In both generations, LTP induction is augmented by a newly appearing cAMP/p38 MAP kinase-dependent signaling cascade. Strikingly, defective LTP and contextual fear conditioning memory normally associated with ras-grf knock-out mice are both masked in the offspring of enriched mutant parents. The transgenerational transmission of this effect occurs from the enriched mother to her offspring during embryogenesis.

Why pay university tuition?

...when you can get an array of astounding courses from places like Academic Earth, with the videos of the lectures shown in your web browser. I recommend the introductory Psychology course offered by Paul Bloom at Yale.

Our genes influence our social networks

Jackson reviews an analysis by Fowler et al. that suggests that genetic traits influence the social behavior of individuals:

...Fowler et al examined the social network characteristics of 1,110 twins from an Adolescent Health Dataset which is based on interviews of high school students. Presuming that the social environment that twins share is not influenced by whether they are monozygotic or dizygotic, if network characteristics are significantly more correlated among monozygotic twins than dizygotic twins then there is evidence for a genetic role in network formation.

The network characteristics that Fowler et al.investigate are: in-degree (how many students name a given student as a friend), out-degree (how many students a given student names as friends), transitivity (if A and B are friends, and B and C are friends, what is the likelihood that A and C are friends), and betweenness centrality (the fraction of shortest paths between other pairs of students that a given student lies on). Their statistical analysis assumes that the variation in a network characteristic can be additively separated into a component that is genetic, a component caused by the environment that would be shared with a twin, and a component caused by the environment that would not be shared with a twin. The covariance between monozygotic twins is then the variance caused by the common environment plus the variance caused by genetic factors, whereas the covariance between dizygotic twins is the variance caused by the common environment plus half of the variance caused by genetic factors. This formulation allows one to solve for the percentage of variation in a given network characteristic that is caused by each of the genetic, common environment, and unshared environment components. The figure shows that almost half of the variation in transitivity and in-degree are genetically attributable, and more than a quarter of betweenness centrality is genetically attributable, but the genetic component of the out-degree variation is too small to be statistically significant. The common environment is statistically insignificant in all cases. (click on figure to enlarge it).

Fowler et al. tried a number of network models to fit with the data and found the only one which generated a relationship between genetics and transitivity was an “Attract and Introduce” model built on two assumptions. First, some individuals are inherently more attractive than others, whether physically or otherwise, so they receive more friendship nominations. Second, some individuals are inherently more inclined to introduce new friends to existing friends (and hence such individuals will indirectly enhance their own transitivity).

Brain correlates of musical improvisation.

Berkowitz and Ansari report an fMRI study of the brains of trained pianists while they are improvising. To get control conditions for comparisons they designed a series of four activities. In the two general types of tasks, they had subjects either improvise melodies or play pre-learned patterns. Comparing brain activity in these two situations allowed them to focus on melodic improvisation. Subjects did each of these two general tasks either with or without a metronome. When there was no metronome marking time, subjects improvised their own rhythms. Comparing conditions with and without metronome allowed them to look at rhythmic improvisation. A key point is that when the subjects played patterns (instead of improvised melodies), they could choose to play them in any order. Thus there was still some spontaneity in decision making, but the choices were more limited than during improvisation.

The authors observed an overlap between melodic improvisation and rhythmic improvisation in three areas of the brain: the dorsal premotor cortex (dPMC), the anterior cingulate (ACC), and the inferior frontal gyrus/ventral premotor cortex (IFG/vPMC). From a summary of the work by Bannatyne:

“The dPMC takes information about where the body is in space, makes a motor plan, and sends it to the motor cortex to execute the plan. The fact [that] it’s involved in improvisation is not surprising, since it is a motor activity. The ACC is a part of the brain that appears to be involved in conflict monitoring — when you’re trying to sort out two conflicting possibilities, like when you to read the word BLUE when it’s printed in the color red. It’s involved with decision making, which also makes sense — improvisation is decision making, deciding what to play and how to play it.” The IFG/vPMC is perhaps one of the most interesting findings of their study. “This area is known to be involved when people speak and understand language. It’s also active when people hear and understand music. What we’ve shown is that it’s involved when people create music.”

Improvising, from a neurobiological perspective, involves generating, selecting, and executing musical-motor sequences, something that wouldn’t surprise musicians. But in terms of brain research, it’s a new piece of information.

Erasing fear responses and preventing the return of fear.

Kindt et al. demonstrate an interesting effect of a beta-blocker that one thinks might become part of clinical practice soon. They found that a conditioned fear response can be weakened by disrupting the reconsolidation of the fear memory with propranolol and that this disruption prevents the return of fear. While Propranolol disrupts the reconsolidation of the fear memory, it does not disrupt declarative memory (recall of the facts of the fear inducing event). The abstract:

Animal studies have shown that fear memories can change when recalled, a process referred to as reconsolidation. We found that oral administration of the -adrenergic receptor antagonist propranolol before memory reactivation in humans erased the behavioral expression of the fear memory 24 h later and prevented the return of fear. Disrupting the reconsolidation of fear memory opens up new avenues for providing a long-term cure for patients with emotional disorders.

Some details:

The conditioned fear response was measured as potentiation of the eyeblink startle reflex to a loud noise (40 ms, 104 dB) by electromyography of the right orbicularis oculi muscle. Stronger startle responses to the loud noise during the fear-conditioned stimulus (CS1⁺) as compared with the control stimulus (CS2^-) reflects the fearful state of the participant elicited by CS1⁺. Startle potentiation taps directly into the amygdala, and fear-conditioning procedures yield highly reliable and robust startle potentiation.


Figure. (click to enlarge) (a–f) Mean startle potentiation to the fear-conditioned stimulus (CS1), the control stimulus (CS2) and noise alone (NA) trials (left) and mean expectancy scores of the unconditioned stimulus to CS1 and CS2 trials (right) during acquisition (trial 1–8), extinction (trial 1–10) and test (trial 1–5) for the placebo (n = 20, a,b), propranolol reactivation (n = 20, c,d) and propranolol without reactivation (n = 20, e,f) group. CS1⁺ refers to the fear conditioned stimulus during acquisition, CS1^- refers to the fear conditioned stimulus during extinction and test, CS1-R refers to the reactivation of the fear conditioned stimulus and CS2^- refers to the control stimulus during all phases of the experiment. Error bars represent s.e.m.

Transcendence from Neuroscience

Clip from a brief essay by Garreau:

....the new vision of transcendence coming out of neuroscience. It’s long been observed that intelligent organisms require love to develop or even just to survive. Not coincidentally, we can readily identify brain functions that allow and require us to be deeply relational with others. There are also aspects of the brain that can be shown to equip us to experience elevated moments when we transcend boundaries of self. What happens as the implications of all this research starts suggesting that particular religions are just cultural artifacts built on top of universal human physical traits?

Genetic determinants of financial risk taking

Here is an interesting bit from Kuhnen and Chiao, although I'm surprised that the reviewers let them get away with using the word 'determinants' rather than 'correlates':

Individuals vary in their willingness to take financial risks. Here we show that variants of two genes that regulate dopamine and serotonin neurotransmission and have been previously linked to emotional behavior, anxiety and addiction (5-HTTLPR and DRD4) are significant determinants of risk taking in investment decisions. We find that the 5-HTTLPR s/s allele carriers take 28% less risk than those carrying the s/l or l/l alleles of the gene. DRD4 7-repeat allele carriers take 25% more risk than individuals without the 7-repeat allele. These findings contribute to the emerging literature on the genetic determinants of economic behavior.