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J. A. Scott Kelso, Emmanuelle Tognoli, Daniela Benites, Gonzalo C. de Guzman Center for Complex Systems and Brain Sciences, Florida Atlantic University, Boca Raton, FL-33431 – USA [email protected] ; [email protected] ; [email protected] ; [email protected] Postdoctoral position opening Applications: [email protected] ; [email protected] I. AIM: Identify dynamic patterns of brain activity involved in social coordination and its breakdown. Social behaviors rest on complex mental/brain states that unfold in time during the course of an interaction. A framework was developed to address this complex temporal dynamics of brains and behaviors (Tognoli & Kelso, 2009; and below). It introduces the notion of dynamical neuromarkers, transient self-organized brain patterns taking on a specific role during social behavior. The goal of this framework is to identify the contribution of dynamical neuromarkers of social behavior: when do they occur, how do they influence later neuromarkers, and what is their unique functional significance. Time (sec) Heuristic: to gain better view on oscilla- tions. Data driven if possible Too narrow: clipping Too broad: poor visualization Inter-individual variability: filter is chosen on a subject-by-subject basis. Filter selects time scales Basic building blocks are self- organized assemblies. Elicit radial (gyrus) or tangen- tial (sulcus) patterns. Key elements are local maxima, spatial and temporal features. Source estimation is aided by 3 key aspects of this frameworks: Reconstruction per- formed on homogene- ous samples of brain dynamics Limited inter-electrode variance in SNR and artifacts (bandpass fil- ter) Prior knowledge (number of source, co- ordination dynamics...) provides constraints Continuous EEG is parsed into segments of homogene- ous oscillatory activity. Each pattern reflects a transient functional network. For each local maximum: Spatial organization, amplitude, fre- quency, phase For the pattern: conditions of occurrence, onset time, offset time, duration phase stability, relative phase, rela- tive frequency For the class: Number of occurrence, conditions of occurrence, cumulative time, cumu- lative amplitude Mining Statistical inference 4.9 5 5.1 5.2 5.3 5.4 5.5 -6 -4 -2 0 2 4 6 case B 3.2 3.3 3.4 3.5 3.6 3.7 3.8 -5 0 5 case C time (sec) 3 3.1 3.2 3.3 3.4 3.5 3.6 3.7 -6 -4 -2 0 2 4 6 case A scatter here scatter here start here ? Model of coordination dynamics speci- fies dynamical regimes: uncoordinated, coordinated inphase, antiphase, out-of- phase, metastable. Predictive forward model provides signature for real and false coordination. Babiloni et al., 2005 Goal is to find association between classes of patterns and behavioral/ mental/clinical states. Further goal is to find association between successive brain states. Transient dynamical states: samples of a recurring functional organization. For small datasets: normative classes For large datasets: ad-hoc taxonomy of brain states II. MATERIALS AND METHODS: Recording of behavior and EEG of two people engaged in intentional social coordination task: Task: perform continuous finger movement during 40 s trials; vision of each other movement controlled by screen that turns transparent at t=20s Three conditions: Inphase coordination (stable relative phase near 0°) Antiphase coordination (stable relative phase near 180°) Intrinsic behavior (each Ss maintain his/her own movement) Finger movements: flexible resistance bend sensors (ImageSI, NY) Dual EEG: dual-60 channel (10 percent system), band-pass 0.1-200Hz, sampled at 1000Hz (Neuroscan TX) 24 subjects (12 pairs), with (corrected to) normal vision, one pair of which is presented here. VI. BETWEEN-BRAIN SYNCHRONIZATION IMPORTANCE OF TRANSITIONS: Transitions are key moments in a dynamical system. In this example (above), transition to synchronization occurs at 3 seconds, caused by subject 2 (red) increasing movement frequency. MOVEMENT DETERMINES BRAIN PATTERN SWITCHES: At transition onset, subjects tend to switch brain patterns at specific phases of movement near peak flexion and peak extension (blue/red arrows in example trial above). Note that patterns switches tend to occur near peak of either one’s own movement or the partner’s. Red histogram above shows subject 2’s tendency to switch functional brain patterns at specific movement phase of her partner during transition to synchronized behavior. BRAIN PATTERNS OF PARTNERS TEND TO SWITCH IN SYNCHRONY: During transitions, subjects also tend to switch patterns in synchrony (see * in example above), irrespective of the content of brain patterns. This tendency is possibly related to partners’ shared attention to salient features of their collective behavior. -600 -400 -200 0 200 400 600 Behavior -10 -5 0 5 10 brain waves subject 1 -10 -5 0 5 10 brain waves subject 2 2.6 2.8 3 3.2 3.4 3.6 -600 -400 -200 0 200 400 600 behavioral synchronization time (sec) * * * * * 0 3.14 0 2 4 6 8 10 12 14 16 18 red brain strobe on blue finger movement -1 -0.5 0 0.5 1 VIII. BRAIN COORDNATION DYNAMICS FRAMEWORK IV. BEHAVIORAL ANALYSIS III. A COMPLEX BEHAVIORAL WEB A number of distal and proximal factors interplay during time course of complex behaviors (intention, context, goal, abilities, preferences, history...). We analyze transitions to synchronized or desynchronized behavior. Each transition is characterized by a set of attributes that describes the transition’s circumstances of occurrence extensively (see left). 288 possibilities V. BRAIN ANALYSIS Continuous brain dynamics is segmented into a succession of patterns. Each brain pattern is classified (27 classes obtained in this experiment). Patterns occurring in the vicinity of transition to synchronized or unsynchronized behavior (0.5 sec before and after transition) are entered in a database. We seek neuromarkers that occur in relation with behavioral variables, especially synchronization~ desynchronization and agency (self~other). Complementary pairs are used as mutual controls. VII. DISCUSSION Social behavior cannot be reduced to a fixed sequence of mental operations: a dynamical framework opens up the possibility to explore the rich interplay of all the system’s variables. We presented the framework of Brain Coordination Dynamics, designed to study complex and temporally-structured aspects of social behavior. We identified candidate neuromarkers of social coordination and its breakdown. Finally, we uncovered a mechanism for synchronization between brain. V. BRAIN ANALYSIS CNT’D
Transcript

J. A. Scott Kelso, Emmanuelle Tognoli, Daniela Benites, Gonzalo C. de Guzman

Center for Complex Systems and Brain Sciences, Florida Atlantic University, Boca Raton, FL-33431 – USA

[email protected] ; [email protected] ; [email protected] ; [email protected]

Postdoctoral position opening Applications:

[email protected] ; [email protected]

I. AIM: Identify dynamic patterns of brain activity involved in social coordination and its breakdown.

Social behaviors rest on complex mental/brain states that unfold in time during the course of an interaction. A framework was developed to address this complex temporal dynamics of brains and behaviors (Tognoli & Kelso, 2009; and below). It introduces the notion of dynamical neuromarkers, transient self-organized brain patterns taking on a specific role during social behavior. The goal of this framework is to identify the contribution of dynamical neuromarkers of social behavior: when do they occur, how do they influence later neuromarkers, and what is their unique functional significance.

Time (sec)

Heuristic: to gain better view on oscilla-tions. Data driven if possible • Too narrow: clipping • Too broad: poor visualization Inter-individual variability: filter is chosen on a subject-by-subject basis. Filter selects time scales

Basic building blocks are self-organized assemblies. Elicit radial (gyrus) or tangen-tial (sulcus) patterns. Key elements are local maxima, spatial and temporal features.

Source estimation is aided by 3 key aspects of this frameworks: • Reconstruction per-

formed on homogene-ous samples of brain dynamics

• Limited inter-electrode variance in SNR and artifacts (bandpass fil-ter)

• Pr i o r knowledg e (number of source, co-ordination dynamics...) provides constraints

Continuous EEG is parsed into segments of homogene-ous oscillatory activity. Each pattern reflects a transient functional network.

For each local maximum: Spatial organization, amplitude, fre-quency, phase

For the pattern: conditions of occurrence, onset time, offset time, duration phase stability, relative phase, rela-tive frequency

For the class: Number of occurrence, conditions of occurrence, cumulative time, cumu-lative amplitude

→ Mining → Statistical inference

4.9 5 5.1 5.2 5.3 5.4 5.5

-6

-4

-2

0

2

4

6

case

B

3.2 3.3 3.4 3.5 3.6 3.7 3.8

-5

0

5

case

C

time (sec)

3 3.1 3.2 3.3 3.4 3.5 3.6 3.7

-6-4-20246

case

A

scatter here

scatter here

start here

?

Model of coordination dynamics speci-fies dynamical regimes: uncoordinated, coordinated inphase, antiphase, out-of-phase, metastable. Predictive forward model provides signature for real and false coordination.

Babiloni et al., 2005

Goal is to find association between classes of patterns and behavioral/mental/clinical states.

Further goal is to find association between successive brain states.

Transient dynamical states: samples of a recurring functional organization. • For small datasets:

normative classes • For large datasets:

ad-hoc taxonomy of brain states

II. MATERIALS AND METHODS: Recording of behavior and EEG of two people engaged in intentional social coordination task: • Task: perform continuous finger movement during 40 s trials; vision of each other

movement controlled by screen that turns transparent at t=20s • Three conditions:

• Inphase coordination (stable relative phase near 0°) • Antiphase coordination (stable relative phase near 180°) • Intrinsic behavior (each Ss maintain his/her own movement)

• Finger movements: flexible resistance bend sensors (ImageSI, NY) • Dual EEG: dual-60 channel (10 percent system), band-pass 0.1-200Hz, sampled at

1000Hz (Neuroscan TX) • 24 subjects (12 pairs), with (corrected to) normal vision, one pair of which is presented

here.

VI. BETWEEN-BRAIN SYNCHRONIZATION

IMPORTANCE OF TRANSITIONS: Transitions are key moments in a dynamical system. In this example (above), transition to synchronization occurs at 3 seconds, caused by subject 2 (red) increasing movement frequency. MOVEMENT DETERMINES BRAIN PATTERN SWITCHES: At transition onset, subjects tend to switch brain patterns at specific phases of movement near peak flexion and peak extension (blue/red arrows in example trial above). Note that patterns switches tend to occur near peak of either one’s own movement or the partner’s. Red histogram above shows subject 2’s tendency to switch functional brain patterns at specific movement phase of her partner during transition to synchronized behavior. BRAIN PATTERNS OF PARTNERS TEND TO SWITCH IN SYNCHRONY: During transitions, subjects also tend to switch patterns in synchrony (see * in example above), irrespective of the content of brain patterns. This tendency is possibly related to partners’ shared attention to salient features of their collective behavior.

-600

-400

-200

0

200

400

600

Beha

vior

-10

-5

0

5

10

brai

n w

aves

sub

ject

1

-10

-5

0

5

10

brai

n w

aves

sub

ject

2

2.6 2.8 3 3.2 3.4 3.6

-600

-400

-200

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beha

viora

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sync

hron

izatio

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time (sec)

* * * * *

0 3.140

2

4

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10

12

14

16

18red brain strobe on blue finger movement

-1

-0.5

0

0.5

1

VIII. BRAIN COORDNATION DYNAMICS FRAMEWORK

IV. BEHAVIORAL ANALYSIS

III. A COMPLEX BEHAVIORAL WEB A number of distal and proximal factors interplay during time course of complex behaviors (intention, context, goal, abilities, preferences, history...). We analyze transitions to synchronized or desynchronized behavior. Each transition is characterized by a set of attributes that describes the t r a ns i t i o n ’s c i r c um s t a n c e s o f occurrence extensively (see left). 288

possibilities

V. BRAIN ANALYSIS Continuous brain dynamics is segmented into a succession of patterns. Each brain pattern is classified (27 classes obtained in th is exper iment ) . Pat terns occurring in the vicinity of transition to synchronized or unsynchronized behavior (0.5 sec before and after transition) are entered in a database. We seek neuromarkers that occur in relation wi th behav io ra l var iab les , especia l ly synchronizat ion~ desynchronization and agency (self~other). Complementary pairs are used as mutual controls.

VII. DISCUSSION Social behavior cannot be reduced to a fixed sequence of mental operations: a dynamical framework opens up the possibility to explore the rich interplay of all the system’s variables. We presented the framework of Brain Coordination Dynamics, designed to study complex and temporally-structured aspects of social behavior. We identified candidate neuromarkers of social coordination and its breakdown. Finally, we uncovered a mechanism for synchronization between brain.

V. BRAIN ANALYSIS CNT’D

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