## Figures

## Abstract

Anatomic connections between brain areas affect information flow between neuronal circuits and the synchronization of neuronal activity. However, such structural connectivity does not coincide with effective connectivity (or, more precisely, causal connectivity), related to the elusive question “Which areas cause the present activity of which others?”. Effective connectivity is directed and depends flexibly on contexts and tasks. Here we show that dynamic effective connectivity can emerge from transitions in the collective organization of coherent neural activity. Integrating simulation and semi-analytic approaches, we study mesoscale network motifs of interacting cortical areas, modeled as large random networks of spiking neurons or as simple rate units. Through a causal analysis of time-series of model neural activity, we show that different dynamical states generated by a same structural connectivity motif correspond to distinct effective connectivity motifs. Such effective motifs can display a dominant directionality, due to spontaneous symmetry breaking and effective entrainment between local brain rhythms, although all connections in the considered structural motifs are reciprocal. We show then that transitions between effective connectivity configurations (like, for instance, reversal in the direction of inter-areal interactions) can be triggered reliably by brief perturbation inputs, properly timed with respect to an ongoing local oscillation, without the need for plastic synaptic changes. Finally, we analyze how the information encoded in spiking patterns of a local neuronal population is propagated across a fixed structural connectivity motif, demonstrating that changes in the active effective connectivity regulate both the efficiency and the directionality of information transfer. Previous studies stressed the role played by coherent oscillations in establishing efficient communication between distant areas. Going beyond these early proposals, we advance here that dynamic interactions between brain rhythms provide as well the basis for the self-organized control of this “communication-through-coherence”, making thus possible a fast “on-demand” reconfiguration of global information routing modalities.

## Author Summary

The circuits of the brain must perform a daunting amount of functions. But how can “brain states” be flexibly controlled, given that anatomic inter-areal connections can be considered as fixed, on timescales relevant for behavior? We hypothesize that, thanks to the nonlinear interaction between brain rhythms, even a simple circuit involving few brain areas can originate a multitude of effective circuits, associated with alternative functions selectable “on demand”. A distinction is usually made between structural connectivity, which describes actual synaptic connections, and effective connectivity, quantifying, beyond correlation, directed inter-areal causal influences. In our study, we measure effective connectivity based on time-series of neural activity generated by model inter-areal circuits. We find that “causality follows dynamics”. We show indeed that different effective networks correspond to different dynamical states associated to a same structural network (in particular, different phase-locking patterns between local neuronal oscillations). We then find that “information follows causality” (and thus, again, dynamics). We demonstrate that different effective networks give rise to alternative modalities of information routing between brain areas wired together in a fixed structural network. In particular, we show that the self-organization of interacting “analog” rate oscillations control the flow of “digital-like” information encoded in complex spiking patterns.

**Citation: **Battaglia D, Witt A, Wolf F, Geisel T (2012) Dynamic Effective Connectivity of Inter-Areal Brain Circuits. PLoS Comput Biol 8(3):
e1002438.
https://doi.org/10.1371/journal.pcbi.1002438

**Editor: **Olaf Sporns, Indiana University, United States of America

**Received: **October 26, 2011; **Accepted: **February 4, 2012; **Published: ** March 22, 2012

**Copyright: ** © 2012 Battaglia et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

**Funding: **We acknowledge financial support by the German Federal Ministry of Education and Research (BMBF) via the Bernstein Center for Computational Neuroscience (BCCN) Göttingen under Grant No. 01GQ1005B. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

**Competing interests: ** The authors have declared that no competing interests exist.

## Introduction

In Arcimboldo's (1527–1593) paintings, whimsical portraits emerge out of arrangements of flowers and vegetables. Only directing attention to details, the illusion of seeing a face is suppressed (Figure 1A–B). Our brain is indeed hardwired to detect facial features and a complex network of brain areas is devoted to face perception [1]. The capacity to detect faces in an Arcimboldo canvas may be lost when lesions impair the connectivity between these areas [2]. It is not conceivable, however, that, in a healthy subject, shifts between alternate perceptions are obtained by actual “plugging and unplugging” of synapses, as in a manual telephone switchboard.

This is illustrated by the example of a Giuseppe Arcimboldo's painting (*Vertumnus*; 1590, Skoklosters Slott, Sweden). A: the illusion of seeing a face is due to the default activation of a network of brain areas dedicated to face recognition. B: however, selective attention to individual components –e.g. to a pear or a flower– suppresses this illusion by modulating the interaction between these and other brain areas. Therefore, effective connectivity, i.e. the specific active pattern of inter-areal influences, needs to be rewired “on demand” in a fast and reliable way, without changes in the underlying structural connectivity between the involved areas.

Brain functions –from vision [3] or motor preparation [4] up to memory [5], attention [6]–[8] or awareness [9]– as well as their complex coordination [10] require the control of inter-areal interactions on time-scales faster than synaptic changes [11], [12]. In particular, strength and direction of causal influences between areas, described by the so-called *effective* connectivity [13]–[15], must be reconfigurable even when the underlying *structural* (i.e. anatomic) connectivity is fixed. The ability to quickly reshape effective connectivity –interpreted, in the context of the present study, as “causal connectivity” [16] or “directed functional connectivity” (see *Discussion*)– is a chief requirement for performance in a changing environment. Yet it is an open problem to understand which circuit mechanisms allow for achieving this ability. How can manifold effective connectivities –corresponding to different patterns of inter-areal interactions, or brain states [17]– result from a fixed structural connectivity? And how can effective connectivity be controlled without resorting to structural plasticity, leading to a flexible “on demand” selection of function?

Several experimental and theoretical studies have suggested that *multi-stability* of neural circuits might underlie the switching between different perceptions or behaviors [18]–[22]. In this view, transitions between many possible attractors of the neural dynamics would occur under the combined influence of structured “brain noise” [23] and of the bias exerted by sensory or cognitive driving [24]–[26]. Recent reports have more specifically highlighted how dynamic multi-stability can give rise to transitions between different oscillatory states of brain dynamics [27], [28]. This is particularly relevant in this context, because long-range oscillatory coherence [12], [29] –in particular in the gamma band of frequency (30–100 Hz) [29]–[32]– is believed to play a central role in inter-areal communication.

Ongoing local oscillatory activity modulates rhythmically neuronal excitability [33]. As a consequence, according to the influential *communication-through-coherence* hypothesis [31], neuronal groups oscillating in a suitable phase coherence relation –such to align their respective “communication windows”– are likely to interact more efficiently than neuronal groups which are not synchronized. However, despite accumulating experimental evidence of communication-through-coherence mechanisms [34]–[38] and of their involvement in selective attention and top-down modulation [30], [39], [40], a complete understanding of how inter-areal phase coherence can be flexibly regulated at the circuit level is still missing. In this study we go beyond earlier contributions, by showing that the self-organization properties of interacting brain rhythms lead spontaneously to the emergence of mechanisms for the robust and reliable control of inter-areal phase-relations and information routing.

Through large-scale simulations of networks of spiking neurons and rigorous analysis of mean-field rate models, we model the oscillatory dynamics of generic brain circuits involving a small number of interacting areas (*structural connectivity motifs* at the mesoscopic scale). Following [41], we extract then the effective connectivity associated to this simulated neural activity. In the framework of this study, we use a data driven rather than a model driven approach to effective connectivity [16] (see also *Discussion* section), and we quantify causal influences in an operational sense, based on a statistical analysis of multivariate time-series of synthetic “LFP” signals. Our causality measure of choice is Transfer Entropy (TE) [42], [43]. TE is based on information theory [44] (and therefore more general than causality measures based on regression [45], [46]), is “model-agnostic” and in principle capable of capturing arbitrary linear and nonlinear inter-areal interactions.

Through our analyses, we first confirm the intuition that “causality follows dynamics”. Indeed we show that our causal analysis based on TE is able to capture the complex multi-stable dynamics of the simulated neural activity. As a result, different *effective connectivity motifs* stem out of different dynamical states of the underlying structural connectivity motif (more specifically, different phase-locking patterns of coherent gamma oscillations). Transitions between these effective connectivity motifs correspond to switchings between alternative dynamic attractors.

We show then that transitions can be reliably induced through brief transient perturbations properly timed with respect to the ongoing rhythms, due to the non-linear phase-response properties [47] of oscillating neuronal populations. Based on dynamics, this neurally-plausible mechanism for brain-state switching is metabolically more efficient than coordinated plastic changes of a large number of synapses, and is faster than neuromodulation [48].

Finally, we find that “information follows causality” (and, thus, again, dynamics). As a matter of fact, effective connectivity is measured in terms of time-series of “LFP-like” signals reflecting collective activity of population of neurons, while the information encoded in neuronal representations is carried by spiking activity. Therefore an effective connectivity analysis –even when based on TE– does not provide an actual description of information transmission in the sense of neural information processing and complementary analyses are required to investigate this aspect. Based on a general information theoretical perspective, which does not require specifying details of the used encoding [44], we consider information encoded in spiking patterns [49]–[53], rather than in modulations of the population firing rate. As a matter of fact, the spiking of individual neurons can be very irregular even when the collective rate oscillations are regular [54]–[57]. Therefore, even local rhythms in which the firing rate is modulated in a very stereotyped way, might correspond to irregular (highly entropic) sequences of codewords encoding information in a digital-like fashion (e.g. by the firing –“1”– or missed firing –“0”– of specific spikes at a given cycle [58]). In such a framework, oscillations would not directly represent information, but would rather act as a carrier of “data-packets” associated to spike patterns of synchronously active cell assemblies. By quantifying through a Mutual Information (MI) analysis the maximum amount of information encoded potentially in the spiking activity of a local area and by evaluating how much of this information is actually transferred to distant interconnected areas, we demonstrate that different effective connectivity configurations correspond to different modalities of information routing. Therefore, the pathways along which information propagates can be reconfigured within the time of a few reference oscillation cycles, by switching to a different effective connectivity motif.

Our results provide thus novel theoretical support to the hypothesis that dynamic effective connectivity stems from the self-organization of brain rhythmic activity. Going beyond previous proposals, which stressed the importance of oscillations for feature binding [59] or for efficient inter-areal “communication-through-coherence”, we advance that the complex dynamics of interacting brain rhythms allow to implement reconfigurable routing of information in a self-organized manner and in a way reminiscent of a clocked device (in which digital-like spike pattern codewords are exchanged at each cycle of an analog rate oscillation).

## Results

### Models of interacting areas

In order to model the neuronal activity of interacting areas, we use two different approaches, previously introduced in [60]. First, each area is modeled as a large network of thousands of excitatory and inhibitory spiking neurons, driven by uncorrelated noise representing background cortical input (*network model*). Recurrent synaptic connections are random and sparse. In these networks, local interactions are excitatory and inhibitory. A scheme of the network model for a local area is depicted in Figure 2A (left). In agreement with experimental evidence that the recruitment of local interneuronal networks is necessary for obtaining coherent gamma cortical activity *in vitro* and *in vivo* [61], [62], the model develops synchronous oscillations () when inhibition is strong, i.e. for a sufficiently large probability of inhibitory connection [54]–[57], [63]. These fast oscillations are clearly visible in the average membrane potential (denoted in the following as “LFP”), an example trace of which is represented in Figure 2A (bottom right). Despite the regularity of these collective rhythms, the ongoing neural activity is only sparsely synchronized. The spiking of individual neurons is indeed very irregular [54], [56] and neurons do not fire an action potential at every oscillation cycle, as visible from the example spike trains represented in Figure 2A (top right). Structural network motifs involving areas are constructed by allowing excitatory neurons to establish in addition long-range connections toward excitatory or inhibitory neurons in a distant target area (see a schematic representation of an structural connectivity motif in Figure 2C). The strength of inter-areal coupling is regulated by varying the probability of establishing an excitatory connection.

A: in the network model, each local area is modeled as a large network of randomly and sparsely interconnected excitatory and inhibitory spiking neurons (inhibitory cells and synapses are in blue, excitatory cells and synapses are in red, ). Individual neurons spike irregularly (see the spike trains of eight representative neurons, top right), but the activity of the network undergoes a collective fast oscillation, visible in the average membrane potential (see example “LFP” trace, bottom right). B: in the rate model, each local area is modeled by a single mean-field rate unit with delayed local inhibition (of strength ). Its dynamics, describing the average area activity, also undergoes a fast oscillation (see example rate trace, right). C–D: the interaction between multiple local areas ( in the case of the reported graphical illustrations, green and orange shading indicate separate areas) is modeled by the dynamics: of multiple local spiking networks, mutually interconnected by long-range excitatory synapses (see panel C); or of multiple rate units, coupled reciprocally by delayed excitation (of strength , see panel D).

In a second analytically more tractable approach, each area is described by a mean-field firing rate variable (*rate model*). The firing rate of a local population of neurons obeys the non-linear dynamical equation (4) (see *Methods*). All incorporated interactions are delayed, accounting for axonal propagation and synaptic integration. Local interactions are dominantly inhibitory (with coupling strength and delay ). Driving is provided by a constant external current. A cartoon of the rate model for a local area is depicted in Figure 2B (left). As in the network model, the firing rates undergo fast oscillations for strong inhibition (, [60]). An example firing rate trace is shown in Figure 2B (right). In order to build structural networks involving areas, different mean-field units are coupled together reciprocally by excitatory long range interactions with strength and delay (see a schematic representation of an structural motif in Figure 2D). Remarkably, the rate model and the network model display matching dynamical states [60] (see also later, Figures 3, 4 and 5). More details on the network and the rate models are given in the *Methods* section and in the Supporting Text S1.

For weak inter-areal coupling strengths, out-of-phase lockings of local periodic oscillations give rise to a family of “unidirectional driving” effective motif. The figure shows dynamics and corresponding effective connectivities for fully symmetric structural motifs with (panels A–B) or (panels C–D) areas. A: the dynamics of interacting areas (green and orange colors) is illustrated by “LFPs” (left, top row) and representative spike trains (left, middle row, two cells per each area) from the network model (horizontal bar is , vertical bar is ), as well as by matching rate traces (left, bottom row) from the rate model (arbitrary time units). The right sub-panel reports the associated effective connectivity measured by Transfer Entropy (TE), evaluated from “LFPs” time-series, for all possible directed interactions (indicated by colored arrows). Boxes indicate the interquartile range and whiskers the confidence interval for the estimated TEs. TEs above the grey horizontal band indicate statistically significant causal influences (see *Methods*). B: to the right of the corresponding box-plot, effective connectivity is also represented in a diagrammatic form. Arrow thicknesses encode the strength of corresponding causal interactions (if statistically significant). Below this effective motif, a second motif in the same unidirectional driving family is plotted (with a smaller size), corresponding to another motif version with equivalent overall topology but reversed directionality. The parameters used for are, for the network model: , ; and for the rate model: , , . C: this panels reports similar quantities as panel A, but now for a structural motif with areas (green, orange and light blue colors). Effective connectivity is now measured by partialized Transfer Entropy (pTE; see *Methods*), in order to account only for direct causal interactions. D: the six effective motifs of the unidirectional driving family for are also reported. The parameters used for are, for the network model: , ; and for the rate model: , , .

The figure shows dynamics and corresponding effective connectivities for fully symmetric structural motifs with (panels A–B) or (panels C–D) areas, for intermediate inter-areal coupling strength, leading to asymmetrically irregular oscillations, phase-locked with an average out-of-phase relation. A: the dynamics of interacting areas (green and orange colors) is illustrated by “LFPs” (left, top row) and representative spike trains (left, middle row, two cells per each area) from the network model (horizontal bar is , vertical bar is ), as well as by matching rate traces (left, bottom row) from the rate model (arbitrary time units). The right sub-panel reports the associated effective connectivity measured by Transfer Entropy (TE), evaluated from “LFPs” time-series, for all possible directed interactions (indicated by colored arrows). Boxes indicate the interquartile range and whiskers the confidence interval for the estimated TEs. TEs above the grey horizontal band indicate statistically significant causal influences (see *Methods*). B: to the right of the corresponding box-plot, effective connectivity is also represented in a diagrammatic form. Arrow thicknesses encode the strength of corresponding causal interactions (if statistically significant). Below this effective motif, a second motif in the same unidirectional driving family is plotted (with a smaller size), corresponding to another motif version with equivalent overall topology but reversed directionality. The parameters used for are, for the network model: , ; and for the rate model: , , . C: this panels reports similar quantities as panel A, but now for a structural motif with areas (green, orange and light blue colors). Effective connectivity is measured by partialized Transfer Entropy (pTE; see *Methods*), in order to account for direct but not for indirect causal interactions. D: the six effective motifs of the unidirectional driving family for are also reported. The parameters used for are, for the network model: , ; and for the rate model: , , .

The figure shows dynamics and corresponding effective connectivities for fully symmetric structural motifs with (panels A–B) or (panels C–D) areas, for large inter-areal coupling strength, leading to symmetrically irregular oscillations, without a stable phase relation. A: the dynamics of interacting areas (green and orange colors) is illustrated by “LFPs” (left, top row) and representative spike trains (left, middle row, two cells per each area) from the network model (horizontal bar is , vertical bar is ), as well as by matching rate traces (left, bottom row) from the rate model (arbitrary time units). The right sub-panel reports the associated effective connectivity measured by Transfer Entropy (TE), evaluated from “LFPs” time-series, for all possible directed interactions (indicated by colored arrows). Boxes indicate the interquartile range and whiskers the confidence interval for the estimated TEs. TEs above the grey horizontal band indicate statistically significant causal influences (see *Methods*). B: to the right of the corresponding box-plot, effective connectivity is also represented in a diagrammatic form. Arrow thicknesses encode the strength of corresponding causal interactions (if statistically significant). A single motif is included in this family The parameters used for are, for the network model: , ; and for the rate model: , , . C: this panels reports similar quantities as panel A, but now for a structural motif with areas (green, orange and light blue colors). Effective connectivity is measured by partialized Transfer Entropy (pTE; see *Methods*), in order to account for direct but not for indirect causal interactions. D: the mutual driving effective motif for is also reported. The parameters used for are, for the network model: , ; and for the rate model: , , .

### Causality follows dynamics

For simplicity, we study fully connected structural motifs involving a few areas (). Note however that our approach might be extended to other structural motifs [64] or even to larger-scale networks with more specific topologies [41], [65].

In the simple structural motifs we consider, delays and strengths of local excitation and inhibition are homogeneous across different areas. Long-range inter-areal connections are as well isotropic, i.e. strengths and delays of inter-areal interactions are the same in all directions. Delay and strength of local and long-range connections can be changed parametrically, but only in a matching way for homologous connections, in such a way that the overall topology of the structural motif is left unchanged. As previously shown in [60], different dynamical states –characterized by oscillations with different phase-locking relations and degrees of periodicity– can arise from these simple structural motif topologies. Changes in the strength of local inhibition, of long-range excitation or of delays of local and long-range connections can lead to phase transitions between qualitatively distinct dynamical states. Interestingly, however, within broad ranges of parameters, multi-stabilities between dynamical states with different phase-locking patterns take place even for completely fixed interaction strengths and delays.

We generate multivariate time-series of simulated “LFPs” in different dynamical states of our models and we calculate TEs for all the possible directed pairwise interactions. We show then that effective connectivities associated to different dynamical states are also different. The resulting effective connectivities can be depicted in diagrammatic form by drawing an arrow for each statistically significant causal interaction. The thickness of each arrow encodes the strength of the corresponding interaction. This graphical representation makes apparent, then, that effective connectivity motifs or, more briefly, *effective motifs*, with many different topologies emerge from structural motifs with a same fixed topology. Such effective motifs are organized into *families*. All the motifs within a same family correspond to dynamical states which are multi-stable for a given choice of parameters, while different families of motifs are obtained for different ranges of parameters leading to different ensembles of dynamical states.

We analyze in detail, in Figures 3, 4 and 5, three families of motifs arising for strong intra-areal inhibition and similarly small values of delays for local and long-range connections. We consider (panels A and B) and (panels C and D) structural motifs. Panels A and C show TEs for different directions of interaction, together with “LFPs” and example spike trains (from the network model), and rate traces (from matching dynamical states of the rate model). Panels B and D display motifs belonging to the corresponding effective motif families.

A first family of effective motifs occurs for weak inter-areal coupling. In this case, neuronal activity oscillates in a roughly periodic fashion (Figure 3A and C, left sub-panel). When local inhibition is strong, the local oscillations generated within different areas lock in an out-of-phase fashion. It is therefore possible to identify a *leader* area whose oscillations lead in phase over the oscillation of *laggard* areas [60]. In this family, causal interactions are statistically significant only for pairwise interactions proceeding from a phase-leading area to a phase-lagging area, as shown by the the box-plots of Figure 3A and C (right sub-panel, see *Discussion* and *Methods* for a discussion of the threshold used for statistical significancy). As commented more in detail in the *Discussion* section, the anisotropy of causal influences in leader-to-laggard and laggard-to-leader directions can be understood in terms of the communication-through-coherence theory. Indeed the longer latency from the oscillations of the laggard area to the oscillations of the leader area reduces the likelihood that rate fluctuations originated locally within a laggard area trigger correlated rate fluctuations within a leading area [35] (see also *Discussion*). Thus, out-of-phase lockings for weak inter-areal coupling give rise to a family of *unidirectional driving* effective motifs. In the case of , causality is significant only in one of two possible directions (Figure 3B), depending on which of the two areas assumes the role of leader. In the case of , it is possible to identify a “causal source” area and a “causal sink” area (see [66] for an analogous terminology), such that no direct or indirect causal interactions in a backward sense from the sink area to the source area are statistically significant. Therefore, the unidirectional driving effective motif family for contains six motifs (Figure 3D), corresponding to all the possible combinations of source and sink areas.

A second family of effective motifs occurs for intermediate inter-areal coupling. In this case, the periodicity of the “LFP” oscillations is disrupted by the emergence of large correlated fluctuations in oscillation cycle amplitudes and durations. As a result, the phase-locking between “LFPs” becomes only approximate, even if it continues to be out-of-phase on average. The rhythm of the laggard area is now more irregular than the rhythm in the leader area. Laggard oscillation amplitudes and durations in fact fluctuate chaotically (Figure 4A and C, left sub-panel). Fluctuations in cycle length do occasionally shorten the laggard-to-leader latencies, enhancing non-linearly and transiently the influence of laggard areas on the leader activity. Correspondingly, TEs in leader-to-laggard directions continue to be larger, but TEs in laggard-to-leader directions are now also statistically significant (Figure 4A and C, right sub-panel). The associated effective motifs are no more unidirectional, but continue to display a dominant direction or sense of rotation (Figure 4B and D). We refer to this family of effective motifs as to a family of *leaky driving* effective motifs (containing two motifs for and six motifs for ).

Finally, a third family of effective motifs occurs for stronger inter-areal coupling. In this case the rhythms of all the areas become equally irregular, characterized by an analogous level of fluctuations in cycle and duration amplitudes. During brief transients, leader areas can still be identified, but these transients do not lead to a stable dynamic behavior and different areas in the structural motif continually exchange their leadership role (Figure 5A and C, left sub-panel). As a result of the instability of phase-leadership relations, only average TEs can be evaluated, yielding to equally large TE values for all pairwise directed interactions (Figure 5A and C, right sub-panel). This results in a family containing a single *mutual driving* effective motif (Figure 5B and D).

Further increases of the inter-areal coupling strength do not restore stable phase-locking relations and, consequently, do not lead to additional families of effective motifs. Note however that the effective motif families explored in Figures 3, 4 and 5 are not the only one that can be generated by the considered fully symmetric structural motifs. Indeed other dynamical configurations exist. In particular, anti-phase locking (i.e. locking with phase-shifts of for and of for ) would become stable when assuming the same interaction delays and inter-areal coupling strengths of Figures 3, 4 and 5, but a weaker local inhibition. Assuming different interaction delays for local and long-range interactions, out-of-phase lockings continue to be very common, but in-phase and anti-phase locking can become stable even for strong local inhibition, within specific ranges of the ratio between local and long-range delays [60]. For , in the case of general delays, more complex combinations can arise as well, like, for instance, states in which two areas oscillate in-phase, while a third is out-of-phase. In-phase locking between areas gives rise to identical TEs for all possible directed interactions, resulting in effective motifs without a dominant directionality. Anti-phase lockings for give rise to relatively large inter-areal phase-shifts and, correspondingly, to weak inter-areal influences (at least in the case of weak inter-areal coupling), resulting in small TE levels which are not statistically significant (not shown). However, in the framework of this study, we focus exclusively on out-of-phase-locked dynamical states, because they are particularly relevant when trying to achieve a reconfigurable inter-areal routing of information (see later results and *Discussion* section).

To conclude, we remark that absolute values of TE depend on specific parameter choices (notably, on time-lag and signal quantization, see *Methods*). However, the relative strengths of TE in different directions –and, therefore, the resulting topology of the associated effective motifs– are rather robust against changes of these parameters. Robustness of causality estimation is analyzed more in detail in the *Discussion* section.

### Spontaneous symmetry breaking

How can asymmetric causal influences emerge from a symmetric structural connectivity? A fundamental dynamical mechanism involved in this phenomenon is known as *spontaneous symmetry breaking*. As shown in [60], for the case of the structural motif, a phase transition occurs at a critical value of the strength of inter-areal inhibition. When local inhibition is stronger than this critical threshold, a phase-locked configuration in which the two areas oscillate in anti-phase loses its stability in favor of a pair of out-of-phase-locking configurations, which become concomitantly stable. The considered structural motif is symmetric, since it is left unchanged after a permutation of the two areas. However, while the anti-phase-locking configuration, stable for weak local inhibition, share this permutation symmetry with the full system, this is no more true for the out-of-phase-locking configurations, stable for strong local inhibition. Note, nevertheless, that the configuration in which leader and laggard area are inverted is also a stable equilibrium, i.e. the complete set of stable equilibria continue to be symmetric, even if individual stable equilibria are not (leading thus to multi-stability). In general, one speaks about spontaneous symmetry breaking whenever a system with specific symmetry properties assumes dynamic configurations whose degree of symmetry is reduced with respect to the full symmetry of the system. The occurrence of symmetry breaking is the signature of a phase transition (of the second order [67]), which leads to the stabilization of states with reduced symmetry.

The existence of a symmetry-breaking phase transition in the simple structural motifs we analyze here (for simplicity, we consider the case) can be proven analytically for the rate model, by deriving the function , which describes the temporal evolution of the phase-shift between two areas when they are weakly interacting [47]:(1)The function for the rate model is shown in the left panel of Figure 6B. Stable phase lockings are given by zeroes of with negative slope crossing and are surrounded by basins of attraction (i.e. sets of configurations leading to a same equilibrium), whose boundaries are unstable in- and anti-phase lockings (Figure 6A). For the network model, a function with an analogous interpretation and a similar shape, shown in the right panel of Figure 6B, can be extracted from simulations, based on a phase description of “LFP” time-series (see *Methods* and Supporting Figure S1A). The analogous distribution of the zero-crossings of and results in equivalent phase-locking behaviors for the rate and network models. Thus spontaneous symmetry breaking leads to multi-stability between alternative out-of-phase-lockings and to the emergence of unidirectional effective driving within a symmetric structural motif.

A: symmetric structural motifs can give rise to asymmetric dynamics in which one area leads in phase over the other (spontaneous symmetry breaking). Basins of attraction (in phase-shift space) of distinct phase-locking configurations are schematically shown here (for ). Empty circles stand for unstable in- and anti-phase lockings and filled circles for stable out-of-phase lockings (corresponding to unidirectional driving effective motifs). B: phase-shift evolution function for the rate model (left, analytical solution, ) and for the network model (right, numerical evaluation, ). Empty and filled circles denote the same stable and unstable phase-lockings as in panel A. C: cartoon of successful (dashed green arrow) and unsuccessful (dashed grey arrow) switchings induced by brief perturbations (lightning icon). An input pulse to the system destabilizes transiently the current phase-locking (solid red and green arrows). For most perturbations, the system does not leave the current basin of attraction and the previous effective motif is restored (dashed red arrow). However, suitable perturbations can lead the system to switch to a different effective motif (dashed green arrow). D: a pulse of strength induces a phase advancement of the collective oscillations, depending on its application phase , as described by the Phase Response Curve (left, rate model; analytical solution, ) or by the induced shift (right, network model; numerical evaluation, ). E–F: frequency histogram of successful switching for pulses applied at different phases (the laggard area is perturbed; for the rate model and for the network model). Predicted intervals for successful switching are marked in green, for the unidirectional (panel E) and for the leaky effective driving (panel F) motifs (left, rate model; right, network model; parameters as in Figures 3 and 4). Diagrams of the induced transitions are shown in the third column (see SI, Figure S2 for perturbations applied to the leader area).

### Control of directed causality

Because of multi-stability, transitions between effective motifs within a family can be triggered by transient perturbations, without need for structural changes. We theoretically determine conditions for such transitions to occur. The application of a pulse of current of small intensity advances or delays the phase of the ongoing local oscillation (see Supporting Figure S1B). This is true for rate oscillations of the mean-field rate model, but also for “LFP” oscillations reflecting rhythmic synchronization in the network model. In the latter case, the collective dynamics is perturbed by synchronously injecting pulse currents into all of the neurons within an area. The induced phase shift depends on the perturbation strength but also on the phase at which the perturbation is applied. For the network model, this can be measured directly from numeric simulations of a perturbed dynamics (see *Methods* and right panel of Figure 6D). For the rate model, the phase shift induced by an instantaneous phased perturbation can be described analytically in terms of the Phase Response Curve (PRC) [47] (see Figure 6D, left, and Supporting Text S1). After a pulse, the phase-shift between two areas is “kicked out” of the current equilibrium locking and assumes a new transient value (solid paths in Figure 6C), which, for weak perturbations and inter-areal coupling, reads:(2)where the approximate equality between square brackets holds for the mean-field rate model. If falls into the basin of attraction of a different phase-locking configuration than , the system will settle within few oscillation cycles into an effective connectivity motif with a different directionality (dashed green path in Figure 6C). Even relatively small perturbations can induce an actual transition, if applied in selected narrow phase intervals in which the induced grows to large values. For most application phases, however, even relatively large perturbations fail to modify the effective driving direction (dashed red path in Figure 6C), because the induced perturbation is vanishingly small over large phase intervals (Figure 6D). This is a robust property, shared by the two (radically different) models we consider here and –we hypothesize– by any local circuit generating fast oscillations through a mechanism based on delayed mutual inhibition. As a consequence, for a given perturbation intensity, a successful switching to a different effective motif occurs only if the perturbation is applied within a specific phase interval, that can be determined analytically from the knowledge of and of for the rate model, or semi-analytically from the knowledge of and (see *Methods*). Figure 6E–F reports the fraction of simulated phased pulses that induced a change of effective directionality as a function of the phase of application of the perturbation. The phase intervals for successful switching predicted by the theory are highlighted in green. We performed simulations of the rate (Figs. 6E–F, left column) and of the network (Figs. 6E–F, middle column) models, for unidirectional (Figs. 6E) and leaky driving (Figs. 6F) effective motifs. Although our theory assumes small inter-areal coupling and is rigorous only for the rate model, the match between simulations and predictions is very good for both models and families of motifs.

In Figs. 6E–F, we perturb the dynamics of the laggard area, but changes in directionality can also be achieved by perturbing the leader area (Supporting Figure S2). Note also that, in the network model, direction switchings can take place spontaneously, due to noisy background inputs. Such noise-induced transitions, however, occur typically on time-scales of the order of seconds, i.e. slow in terms of biologic function, because the phase range for successful switching induction is narrow.

### Effective entrainment

A second non-linear dynamic mechanism underlying the sequence of effective motifs of Figures 3 and 4 is *effective entrainment*. In this phenomenon, the complex dynamics of neural activity seems intriguingly to be dictated by effective rather than by structural connectivity.

We consider as before a rate model of reciprocally connected areas (Figure 2D). In order to properly characterize effective entrainment, we review the concept of *bifurcation diagram* [68]. As shown in [60], when the inter-areal coupling is increased, rate oscillations become gradually more complex (cfr. Figure 7A), due to the onset of deterministic chaos (see also [69] for a similar mechanism in a more complex network model). For small , oscillations are simply periodic (e.g. ). Then, for intermediate (e.g. ), the peak amplitudes of the laggard area oscillation assume in alternation a small number of possible values (period doubling). Finally, for larger (e.g. ), the laggard peak amplitudes fluctuate in a random-like manner within a continuous range. This sequence of transitions can be visualized by plotting a dot for every observed value of the peak amplitudes of oscillation cycles, at different values of . The accumulation of these dots traces an intricate branched structure, which constitutes the bifurcation diagram (Figure 7B).

A: examples of rate oscillations for different values of the inter-areal coupling in the rate model (, , from bottom to top). Filled circles denote peaks of oscillation cycles, different color fillings denote different peak amplitudes. B: The oscillatory dynamics is qualitatively altered by increasing inter-areal coupling, as visualized by bifurcation diagrams, constructed by plotting different peak amplitudes at constant , as different dots (the dots corresponding to the peak amplitudes in panel A, are highlighted also here by filled circles of matching colors). Varying in a continuous range, these dots trace a complex branched structure, denoting emergence of novel dynamical states. The bifurcation diagrams for the case of two symmetrically connected areas (top) and two unidirectionally connected areas (bottom) are very similar. For a symmetric structural motif, spontaneous symmetry breaking leads to effective entrainment, mimicking the direct entrainment, which occurs for an asymmetric unidirectional structural motif. Leader and laggard areas in effective entrainment behave similarly to the driver and driven area in direct entrainment (orange and green bifurcation diagrams, respectively). Note that different structural motifs give rise to equivalent effective motifs (see side diagrams). Note: a different version of panel B was previously published in [60] as Supplementary Figure F.

Bifurcation diagrams for the leader and for the laggard area are plotted in Figure 7B (top panel, in orange and green color, respectively). We compare these bifurcation diagrams with the analogous diagrams constructed in the case of two *unidirectionally* coupled oscillating areas. Qualitatively similar bifurcation sequences are associated to the dynamics of the laggard area (bidirectional coupling) and of the driven area (unidirectional coupling, Figure 7B, bottom panel, green color), for not too strong inter-areal couplings. In the case of unidirectional coupling, the peak amplitudes of the unperturbed driver area oscillations do not fluctuate at all. Therefore, the corresponding bifurcation diagram is given by a constant line (Figure 7B, bottom panel, orange color). In the case of bidirectional coupling, the peak amplitudes of the leader area oscillations undergo fluctuations, but only with a tiny variance. Thus, the corresponding bifurcation diagram has still the appearance of a line, although now “thick” and curved (zooming would reveal bifurcating branches). Note that, for unidirectional coupling, the structural connectivity is explicitly asymmetric. The periodic forcing exerted by the driving area is then known to entrain the driven area into chaos [70]. Such direct entrainment is the *dynamical cause* of chaos. On the other hand, for bidirectional coupling, the structural connectivity is symmetric. However, due to spontaneous symmetry breaking, the resulting effective connectivity is asymmetric and the system behaves *as if* the leader area was a driver area, entraining the laggard area into chaos being only negligibly affected by its back-reaction. Such effective entrainment can be seen as an *emergent dynamical cause* of chaos. Thus, the dynamics of a symmetric structural motif with asymmetric effective connectivity and of a structural motif with a matching asymmetric topology are equivalent.

For a sufficiently strong inter-areal coupling, symmetry in the dynamics of the bidirectional structural motif is suddenly restored [60], in correspondence with a transition to the mutual driving family of effective motifs (Figure 5). As a result, in absence of symmetry breaking, effective driving cannot anymore take place. Thus, for a too strong inter-areal coupling, the emergent anisotropy of effective connectivity is lost, and, with it, the possibility of a dynamic control of effective connectivity (at least via the previously discussed strategies).

### Information follows causality

Despite its name, Transfer Entropy is not directly related to a transfer of information in the sense of neuronal information processing. The TE from area to area measures indeed just the degree to which the knowledge of the past “LFP” of reduces the uncertainty about the future “LFP” of [43], [71]. As a matter of fact, however, the information stored in neural representations must be encoded in terms of spikes, independently from the neural code used. Therefore, it is important to understand to which extent an effective connectivity analysis based on “macroscopic” dynamics (i.e. TEs estimated from “LFPs”) can pretend to describe actual “microscopic” information transmission (i.e. at the level of spiking correlations).

In order to address this issue, we first introduce a framework in which to quantify the amount of information exchanged by interacting areas. In the case of our model, *rate fluctuations* could encode only a limited amount of information, since firing rate oscillations are rather stereotyped. On the other hand, a larger amount of information could be encoded based on *spiking patterns*, since the spiking activity of single neurons is very irregular and thus characterized by a large entropy [44], [58]. As illustrated by Figure 8A, a code can be built, in which a “1” or a “0” symbol denote respectively firing or missed firing of a spike by a specific neuron at a given oscillation cycle. Based on such an encoding, the neural activity of a group of neurons is mapped to digital-like streams, “clocked” by the ongoing network rhythm, in which a different “word” is broadcast at each oscillation cycle. Note that we do not intend to claim that such a code is actually used in the brain. Nevertheless, we introduce it as a theoretical construct grounding a rigorous analysis of information transmission.

A: in the case of sparsely synchronized oscillations, individual neurons fire irregularly (see four example spike trains, middle row) even when the local area activity undergoes a very regular collective rhythm (evident in “LFP” traces, bottom row). Therefore, a large amount of information can be potentially encoded, at every (analog) oscillation cycle, in the form of (digital-like) codewords in which “1” or “0” entries denote respectively firing or missed firing of a specific neuron in the considered cycle (top row). B: the strength of specific subsets of long-range excitatory synapses is systematically enhanced in order to form unidirectional “transmission lines” (TLs) embedded into the symmetric structural motif (see *Methods*). Cells and synapses belonging to TLs are highlighted by pale green (“green-to-orange” area direction) and lilac (“orange-to-green” area direction) colors. Communication efficiency along TLs is quantified by the Mutual Information () between spike trains of pairs of source and target cells connected directly by a TL synapse, normalized by the entropy () of the source cell. C–D: boxplots (see Figures 3, 4 and 5) of for different groups of interconnected cells and for different active effective motifs. Pale green and lilac arrows below the boxplots indicate pairs of cells interconnected by the TL marked with the corresponding color. A dot indicates control pairs of cells interconnected by ordinary weak long-range synapses. Green and orange arrows indicate the dominant directionality of the active effective connectivity motif. C: unidirectional driving effective motif family. Communication efficiency is enhanced only along the TL aligned to the directionality of the active effective connectivity, while it is undistinguishable from control along the other TL. D: leaky driving effective motif family. Communication efficiency is enhanced along both TLs, but more along the TL aligned to the dominant directionality of the active effective connectivity.

We focus here on the fully symmetric structural motif of areas of Figure 2C. We modify the network model considered in the previous sections by embedding into it *transmission lines* (TLs), i.e. mono-directional fiber tracts dedicated to inter-areal communication (see Figure 8B). In more detail, selected sub-populations of *source* excitatory neurons within each area establish synaptic contacts with matching *target* excitatory or inhibitory cells in the other area, in a one-to-one cell arrangement. Synapses in a TL are strengthened with respect to usual synapses, by multiplying their peak conductance by a multiplier (see *Methods* section). Such multiplier is selected to be large, but not too much, in order not to affect the phase-relations between the collective oscillations of the two areas. Indeed, selecting a too large would lead to an in-phase-locking configuration in which collective dynamics is enslaved to the synchronous activity of source and target populations. As analyzed in the Supporting Figure S3, a suitable tuning of ensures that source-to-target neuron communication is facilitated as much as possible, without disrupting the overall effective connectivity (associated to the unperturbed phase-locking pattern). Note that such TL synapses are here introduced as a heuristic device, allowing to maximize the potential capacity of inter-areal communication channels [44]. However, due to the occurrence of consistent spike-timing relations in out-of-phase locked populations, it might be that spike-timing-dependent plasticity [72] lead to the gradual emergence of subsets of synapses with substantially enhanced weight [73], which would play a role in inter-circuit communication very similar to TL synapses.

The information transmission efficiency of each TL, for the case of different effective motifs, is then assessed by quantifying the Mutual Information (MI) [44], [58] between the “digitized” spike trains of pairs of source and target cells (see *Methods*). Since a source cell spikes on average every five or six oscillation cycles, the firing of a single neuron conveys of information per oscillation cycle. MI normalized by the source entropy H indicates how much of this information reaches the target cell, a normalized MI equal to unity denoting lossless transmission. As shown by Figure 8C–D, the communication efficiency of embedded TLs depends strongly on the active effective motif. In the case of unidirectional driving effective motifs (Figure 8C), communication is nearly optimal along the TL aligned with the effective connectivity. For the misaligned TL, however, no enhancement occurs with respect to control (i.e. pairs of connected cells not belonging to a TL). In the case of leaky driving effective motifs (Figure 8D), communication efficiency is boosted for both TLs, but more for the TL aligned with the dominant effective direction. For both families of effective motifs, despite the strong anisotropy, the communication efficiencies of the two embedded TLs can be “swapped” within one or two oscillation cycles, by reversing the active effective connectivity through a suitable transient perturbation (see Figure 6E–F). The considered structural motif acts therefore as a “diode” through which information can propagate efficiently only in one (dynamically reconfigurable) direction determined by effective connectivity.

## Discussion

### Mechanisms for effective connectivity switching

We have shown that a simple structural motif of interacting brain areas can give rise to multiple effective motifs with different directionality and strengths of effective connectivity, organized into different families. Such effective motifs correspond to distinct dynamical states of the underlying structural motif. Beyond this, dynamic multi-stability makes the controlled switching between effective motifs within a same family possible without the need for any structural change.

On the contrary, transitions between effective motifs belonging to different families (e.g. a transition from a unidirectional to a leaky driving motif) cannot take place without changes in the strength of the delay of inter-areal couplings, even if the overall topology of the underlying structural motif does not need to be modified. Each specific effective motif topology (i.e. motif family) is robust within broad ranges of synaptic conductances and latencies, however if parameters are set to be close to critical transition lines separating different dynamical regimes, transitions between different families might be triggered by moderate and unspecific parameter changes. This could be a potential role for neuromodulation, known to affect the net efficacy of excitatory transmission and whose effect on neural circuits can be modeled by coordinated changes in synaptic conductances [74], [75].

Note that dynamical coordination of inter-areal interactions based on precisely-timed synchronous inputs would be compatible with experimental evidence of phase-coding [76]–[81], indicating a functional role for the timing of spikes relative to ongoing brain rhythms (stimulus-locked [82], [83] as well as stimulus-induced or spontaneous [84]). Note also that the time of firing is potentially controllable with elevated precision [85]–[87] and has been found to depend on the phase of LFPs in local as well as in distant brain areas [37].

In general, control protocols different from the one proposed here might be implemented in the brain. For instance, phased pulses might be used as well to stabilize effective connectivity in the presence of stronger noise. Interestingly, the time periods framed by cycles of an ongoing oscillation can be sliced into distinct functional windows in which the application of the same perturbation produces different effects.

Finally, in addition to “on demand” transitions, triggered by exogenous –sensory-driven– or endogenous –cognitive-driven– control signals, noise-driven switching between effective motifs might occur spontaneously, yielding complex patterns of activity during resting state [26], [88], [89].

### Transfer Entropy as a measure of effective connectivity

As revealed by our discussion of spontaneous symmetry breaking and effective entrainment, an analysis based on TE provides a description of complex inter-areal interactions compliant with a dynamical systems perspective. It provides, thus, an intuitive representation of dynamical states that is in the same “space” as anatomical connectivity.

Note that it is currently debated whether TE should be considered as a measure of effective connectivity in strict sense [13], [15], or, rather, of yet another type of connectivity beyond functional connectivity (that could be dubbed causal connectivity [16], [66] or directed functional connectivity). Our position is that TE constitutes, at least in the context of the present study, a measure of effective connectivity in proper sense. Indeed, as indicated by the analysis of Figure 8C–D, the connectivity motifs inferred by TE correctly represent characteristic dynamic mechanisms, like spontaneous symmetry breaking or asymmetric chaos [60], enabling specifically associated modalities of inter-areal information transmission. Therefore, we can conclude that causality (as inferred by TE) follows dynamics (by representing the action of corresponding dynamic mechanisms).

TE constitutes thus a model-free approach (although, non “parameter-free”, cfr. forthcoming section and Figure 9) to the effective connectivity problem, suitable for exploratory data-driven analyses. In this sense it differs from regression-based methods like usual implementations of Granger Causality (GC) [45], [46] or from Dynamic Causal Modeling (DCM) [90], which are model-driven [15], [16], [91]. Strategies like DCM, in particular, assume prior knowledge about the inputs to the system and works by comparing the likelihood of different a priori hypotheses about interaction structures. Such an approach has the undeniable advantage of providing a direct description of actual mechanisms underlying effective connectivity changes (the stimulus-dependence of effective couplings is indeed modeled phenomenologically). However, it might be too restrictive (or arbitrary) when the required a-priori information is missing or highly uncertain. TE, on the contrary: does not require any hypothesis on the type of interaction; should be able to detect even purely non-linear interactions and should be robust against linear cross-talk between signals [92]. These features, together with the efficacy of TE for the causal analysis of synthetic time-series, advocate for a more widespread application of TE methods to real neural data [93]–[95] (at the moment limited by the need of very long time-series [92]).

A–C: The matrices in these panels illustrate the dependence of TE (network model, fully symmetric structural motif, cfr. Figures 3, 4 and 5) on the number of discretization bins used to describe the time-series of neural activity and on the adopted time lag between the time-series (see *Methods*). The matrices in the first two columns (from the left) report TEs in the two possible interaction directions, and , and the matrices in the third column visualize the causal unbalancing (), which quantifies the asymmetry between causal influences in the two directions (see *Methods*). All of these quantities are evaluated for different combinations of and . The vertical axes of the matrices correspond to the range bins and the horizontal axes to the range . This range of time lags corresponds approximately to three oscillation periods. Horizontal scale lines indicate the average oscillation period (, respectively for panels A, B and C). Values of TE and are color-coded (see color bars at the bottom, note the two different color scales for TE and ). Black dotted lines in the matrices enclose regions in which or rise above the threshold for significancy of the corresponding causal interaction (see *Methods*). These significance contours are overlayed in the corresponding matrix. A star denotes the combination of and used for the analysis throughout the main article (, ). Different rows report TE matrices for different effective motifs. A: unidirectional driving effective motif. B: leaky driving effective motif. C: mutual driving effective motif. Diagrams of these effective motifs are drawn in the fourth column as a visual reference. All other parameters are as for the analyses of Figures 3, 4 and 5.

Note that we do not intend to claim superiority of TE in some general sense. As a matter of fact TE is equivalent to GC, as far as the statistics of the considered signals are gaussian [71]. Furthermore, non-linear generalizations of GC and DCM [96]–[99] might be able to capture at a certain extent the complex self-organized dynamics of the neural activity models analyzed in the present study. However, a systematic comparison of the performance of different methods in capturing causal connectivity of realistic non-linear models of neural dynamics goes beyond the focus of the present study and is deferred to future research.

We finally would like to stress, to avoid any potential confusion, that the structural motifs analyzed in the present study are well distinct from causal graphical models of neural activity, in the statistical sense proper of DCMs [90], [100]. They constitute indeed actual mechanistic models of interacting populations of spiking neurons, with a highly non-linear dynamics driven by background noise. Connections in these models are model synapses, i.e. mere structural couplings, not phenomenological effective couplings. Thus, effective connectivity is not constrained a priori, as in DCMs, but is an emergent property of network dynamics, consistent with the existence of effective motif topologies different from the underlying structural topology.

### Robustness of Transfer Entropy estimation

The effective connectivity analyses presented in this study were conducted by evaluating TEs under specific parameter choices. However, absolute values of TE depend on parameters, like, notably, the resolution at which “LFP” signals are quantized and the time-lag at which we probe causal interactions. As discussed in detail in the *Methods* section, estimation of TE requires the sampling of joint distributions of “LFP” values in different areas at different times. Such distributions are sampled as histograms, based on discrete multi-dimensional binning. In practice, each “LFP” time-series is projected to a stream of symbols from a discrete alphabet, corresponding to different quantization levels of the continuous “LFP” signals [101]. The actual number of used bins is a free parameter, although some guiding criteria for its selection do exist [43]. Concerning time-lag , our TE analysis (conducted at the first Markov order [42], following [41], [94]) describes predictability of “LFPs” at time based on “LFPs” at time . The used time-lag is once again a free parameter. To deal with this arbitrariness in parameter choices, we explore systematically the dependence of TE estimations from the aforementioned parameters, by varying both and in a wide continuous range. Figure 9 summarizes the results of this analysis, for three different effective motifs.

Considering the dependency on time-lag , a periodic structure is clearly noticeable in the TE matrices reported in Figure 9. TE values tend to peak in precise bands of , related to latencies between the oscillations of different areas. The analysis of the unidirectional driving motif (Figure 9A), associated to leader-laggard periodic configurations, is particularly transparent (and has a high pedagogic value). Two characteristic time-lags can be defined: a “short” lag , given by the time-shift from oscillation peaks of the leader area to oscillation peaks of the laggard area ; and a “long” lag, , given by the time-shift from laggard to leader oscillation peaks (here, is an average oscillation period, common to both areas leader and laggard areas and ). TE in the direction from leader to laggard, , peaks for the first time at a time-lag (and then at lags , where is a positive integer). TE in the direction from laggard to leader, , peaks first at a time-lag (and then at lags ). If the “LFP” signals were deterministic and *strictly* periodic, the quantities and would be identical (and diverging for infinite precision [42]). However “LFP” signals are only periodic *on average* and have a stochastic component, due to the joint effect of random network connectivity and noisy background inputs. This stochastic component is responsible for small cycle-to-cycle fluctuations in the amplitude of “LFP” oscillation peaks. As discussed more in depth in a next subsection, the efficiency with which fluctuations in the output of a local area can induce (i.e., can “cause”) fluctuations of the output of a distant interconnected area depends on the instantaneous local excitability of this target area, which is undergoing a rhythmic modulation due to the ongoing collective oscillation [31], [33]. As a result, TE can reach different peak values in different directions (and, as a matter of fact, ).

Considering then the dependence on signal quantization, we observe that TE values tend to grow for increasing number of bins , i.e. for a finer resolution in tracking “LFP” amplitude variations. This can be once again understood in terms of the temporal structure of “LFP” signals. As just mentioned, dynamic correlations between small “LFP” amplitude fluctuations carry information relevant for causality estimation. This information would be completely lost by using a too small number of bins for TE evaluation, given that the largest contribution to the dynamic range of “LFP” signals is provided by its fairly stereotyped oscillatory component. Conversely, using a too large number of bins would lead to under-sampling artifacts (therefore, we do not consider the use of more than quantization bins).

By evaluating a threshold for statistical significance independently for each direction and combination of and , we find that, for weak inter-areal coupling, TE never goes above this threshold in the laggard-to-leader direction (Figure 9A). We are also unable to find any choice of and such that, for intermediate inter-areal coupling, TE in the laggard-to-leader direction becomes larger or equal than TE in leader-to-laggard direction (Figure 9B). Looking at matrices of the causal unbalancing (see *Methods*, and Figure 9, third column), we see indeed that, for weak and intermediate coupling strengths, effective connectivity is *robustly asymmetric* in the parameter regions in which causal interactions are statistically significant. Effective connectivity is on the contrary balanced for strong inter-areal coupling (Figure 9C).

We can thus summarize the previous statements by saying that absolute values of TE depend on the choices of and , but that the topology of the resulting effective motif does not (at least in the wide range considered for this robustness analysis).

### Self-organized control of communication-through-coherence

Traditionally, studies about communication-through-coherence or long-range binding between distant cell assemblies have emphasized the importance of in-phase locking (see, e.g. [35], [102]). Although, as previously mentioned, in-phase locking (as well as anti-phase locking) can also arise in our models for different choices of coupling delays and inhibition strengths [60], we decided in the present study to focus on out-of-phase lockings. The case of spontaneous symmetry breaking is indeed particularly interesting, because it underlie the emergence of a dominant directionality in the causal influences between areas reciprocally coupled with comparable strengths. Furthermore, spontaneous symmetry breaking is responsible for the multi-stability between effective connectivity configurations, thus opening the way to a self-organized control of inter-areal interactions [11], [12].

In particular, our study confirms that the reorganization of oscillatory coherence might regulate the relative weight of bottom-up and top-down inter-areal influences [17], [30] or select different interaction modes within cortical networks involving areas of similar hierarchical level, as in the case of motor preparation or planning [4], [103] or language [104].

As a next step, we directly verified that “information follows causality”, since changes in effective connectivity are paralleled by reconfiguration of inter-areal communication modalities. Following [32], [35], we explain the anisotropic modulations of communication efficiency (see Figure 8) in terms of a *communication-through-coherence* mechanism. In fact, because of the out-of-phase locking between rhythms, spikes emitted by neurons in a phase-leading area reach neurons in a phase-lagging area at a favorable phase in which they are highly excitable. Conversely, spikes emitted by neurons in a phase-lagging area reach neurons in a phase-leading area when they are strongly hyperpolarized by a preceding peak of synchronous inhibition. This same mechanism underlie also the anisotropy of “LFP”-based TE, since “LFP” fluctuations are the manifestation (at least in our model) of local population firing rate fluctuations.

Therefore, by combining TE analyses of “LFP”-based effective connectivity with MI analyses of spike-based information transmission, we are able to establish a tight link between control of effective connectivity and control of communication-through-coherence, both of them being emergent manifestations of the self-organized dynamics of interacting brain rhythms.

To conclude, we also note that similar mechanisms might be used beyond the mesoscale level addressed here. Multi-stabilities of structural motifs might be preserved when such motifs are interlaced as modules of a network at the whole-brain level [64]. Likewise, dynamic control of information routing between neuronal clusters [73], [105] or even single cells might occur within more local microcircuits [106], [107].

### Communication-through-coherence beyond rate coding

The previous discussions suggest that oscillations, rather than playing a direct role in the representation of information, would be instrumental to the reconfigurable routing of information encoded in spiking activity. Original formulations of the communication-through-coherence hypothesis [31] suggested that oscillatory coherence facilitates the transmission of local fluctuations of firing rate to a distant site, thus assuming implicitly a rate-based encoding of information in neuronal activity. However, more complex coding mechanisms based on patterns of precisely timed spikes might be achievable by biologically-plausible neuronal circuits [85], [86].

As a matter of fact, our study reveals that the inherent advantages of “labelled-line” codes [51], [108] (in which the information about which local neuron is firing is preserved) –i.e., notably, an augmented information capacity with respect to “summed-population” codes– might be combined with the flexibility and the reliability offered by the communication-through-coherence framework. Indeed, as shown by the analyses of Figure 8, suitable inter-areal phase relations make possible the transmission of information encoded in detailed spiking correlations, rather than just in population firing rate fluctuations.

This is particularly interesting, since many cortical rhythms are only sparsely synchronized, with synchronous oscillations evident in LFP, Multi-Unit Activity or intracellular recordings but not in single unit spike trains [109]–[111]. Such sparse firing might possibly reflect population-coding of behaviorally-relevant information transcending rate-based representations [49]–[53]. Independently from the complexity of these hypothetic representations, our study shows that self-organized communication-through-coherence would have the sufficient potential to dynamically route the rich information that these representations might convey.

### Perspectives

It is very plausible that flexible inter-areal coordination is achieved in the brain through dynamic self-organization [11] as in our models. However, qualitatively different mechanisms than symmetry breaking might contribute to the generation of dynamic effective connectivity in other regimes of activity. Despite sparse synchronization, the level of coherence in our model neuronal activity is larger than in many brain oscillations. However, our results might be generalized to activity regimes in which synchronization is weaker. Phase-relations have been shown to impact effective connectivity even in essentially asynchronous regimes [112]. It would be interesting to understand whether the dominant directionality of effective connectivity can be controlled when out-of-phase locking is only transient [12], [41].

Another open question is whether our theory can be extended to encompass the control of effective connectivity across multiple frequency bands [94]. This is an important question since top-down and bottom-up inter-areal communication might exploit different frequency channels, possibly due to different anatomic origins of ascending and descending cortico-cortical connections [113].

Finally, we are confident that our theory might inspire novel experiments, attempting to manipulate the directionality of inter-areal influences via local stimulation applied conditionally to the phase of ongoing brain rhythms. Precisely timed perturbing inputs could indeed potentially be applied using techniques like electric [114] or optogenetic [115] microstimulation, especially in closed-loop implementations with millisecond precision [116], [117].

## Methods

### Network model

Each area is represented by a random network of excitatory and inhibitory Wang-Buzsáki-type conductance-based neurons [118]. The Wang-Buzsáki model is described by a single compartment endowed with sodium and potassium currents. Note that results (not shown) of simulations performed with a more realistic ratio of excitatory and inhibitory neurons per population would lead to qualitatively similar results with small parameter adjustments (using, for instance, parameters as in [69]).

The membrane potential is given by:(3)where is the capacitance of the neuron, is a leakage current, is an external noisy driving current (due to background Poisson synaptic bombardment), and and are respectively a sodium and a potassium current, depending non linearly on voltage. The last input term is due to recurrent interactions with other neurons in the network. Excitatory synapses are of the AMPA-type and inhibitory synapses of the GABA-type and are modeled as time-dependent conductances. A complete description of the model and a list of all its parameters are given in the Supporting Text S1. “LFP” is defined as the average membrane potential over the cells in each area.

Short-range connections within a local area from population to population are established randomly with probability , where and can be either one of the type (excitatory) or . The excitatory populations are allowed also to establish connections toward populations and in remote areas (). Such long-range connections are established with a probability (). For simplicity, however, we assume that and that . For each of the considered dynamical states, probabilities of connection are provided in the corresponding figure caption.

### Network model with embedded transmission lines (TLs)

First, a structural motif of interconnected random networks of spiking neurons is generated, as in the previous section. Then, on top of the existing excitatory long-range connections, additional stronger long-range connections are introduced in order to form directed transmission lines. In each area a source sub-population, made out of 400 excitatory neurons, and a non-overlapping target sub-population, made out of 200 excitatory and 200 inhibitory neurons, are selected randomly. Excitatory cells in the source populations get connected to cells in the target sub-populations of the other area via strong synapses. These connections are established in a one-to-one arrangement (e.g. each source cell establishes a TL-synapse with a single target cell that does not receive on its turn any other TL-synapse).

The peak conductance of TL-synapses is times stronger than the normal excitatory peak conductance . For the simulations with TL (Figure 8 of the main paper), we set respectively for the unidirectional and for the leaky driving effective motifs. Such unrealistically strong peak conductances, whose purpose is to optimize information transfer by enhancing spiking correlations, can be justified by supposing that each source neuron establishes multiple weaker synaptic contacts with the same target neuron. The multiplier is selected to be as large as possible without altering the original out-of-phase locking relations between the two populations (Figure S3A). Concretely, is tuned by raising it gradually until when a critical point is reached in which the populations lock in-phase (Figure S3C). Then, is set to be just below this critical point (Figure S3B).

### Rate model

Each area is represented by a single rate unit. The dynamical equations for the evolution of the average firing rate in an area are given by:(4)Here, if , and zero otherwise. A constant current represents a background input, stands for the strength of intra-areal inhibition, for the strength of inter-areal excitation and and are the delays of the local and long-range interactions, respectively. We consider in this study only fully symmetric structural motifs of mutually connected areas. For each of the considered dynamical states, the values of , , and are provided in the figure caption.

### Phase reduction and response

Given an oscillatory time-series of neuronal activity, generated indifferently by a rate or by a network model, a phase , for , is linearly interpolated over each oscillation cycle. Here denotes the start time of the oscillation cycle. Note that this definition does not require that the oscillation is periodic: this empiric phase “elastically” adapts to fluctuations in the duration of oscillation cycles (see Supporting Figure S1A).

The phase shift induced by a pulse perturbation (see Supporting Figure S1B) is described by the Phase Response Curve (PRC) (see Eq. (2) and [47]). For the rate model, the PRC can be evaluated analytically if certain general conditions on the relation between the oscillation period and the local inhibition delay are fulfilled [60]. Analytical expressions for the PRC of the rate model, as plotted in Figure 6D (left), are reported in the Supporting Text S1.

In the network model, it is possible to evaluate the phase-shift induced by a perturbation, by directly simulating the effects of this perturbation on the oscillatory dynamics. A perturbation consists of a pulse current of strength injected synchronously into all neurons of one area at a phase of the ongoing local oscillation. The induced phase-shift is estimated by comparing the phases of the perturbed and of the unperturbed oscillations, when a new equilibrium is reached after the application of the perturbation. In detail, since the “LFP” time-series are not strictly periodic and the phase relation is fixed only on average, the average time-lag between the perturbed and the unperturbed “LFPs” is measured by computing their crosscorrelogram over 50 oscillation cycles, starting from the 10-th cycle after the perturbation. This average time lag (readable from the position of the crosscorrelogram peak) is then translated into a phase-shift, by dividing it by the average period (estimated through autocorrelation analysis of the perturbed and unperturbed time-series over the same observation window). Vanishingly small perturbations do not induce long-lasting phase-shifts. Therefore, moderately large perturbation strengths have to be used. In this case, the dependence of on is sensibly non-linear. As a consequence, we evaluate directly the resulting for the used perturbation strength , plotted in Figure 6D (right). The qualitative shape of however does not depend strongly on . In particular, changes of affect the amplitude of the maximum phase-shift but not the perturbation phase for which it occurs. The curve is evaluated point-wise by applying perturbations at 100 different phases within a cycle. For each given phase, the perturbation is applied 100 times to 100 different cycles and the corresponding phase-shifts are averaged. Confidence intervals for are determined phase-by-phase by finding the 2.5-th and the 97.5-th percentile of the induced phase-shift distribution across these 100 trials.

### Phase locking

For simplicity, we focus in the following on the case of areas, although our approach can be extended to larger motifs. The instantaneous phase-difference between two areas and is given by . For vanishing inter-areal coupling, the time evolution of is described by Eq. (1). The term is a functional of the phase response and of the limit cycle waveform of the uncoupled oscillating areas. For the rate model, is determined from analytic expressions of and of the rate oscillation limit cycle (note that the dependence on is replaced by a dependence on after phase-reduction) for . It can be expressed as , with:(5)The resulting expression is reported in the Supporting Text S1 and plotted in Figure 6B (left). Given Eq. (1), the phase shifts between the two areas and in stable phase-locked states correspond to top-down zero-crossings of the functional (i.e. zeroes with negative tangent slope, ).

For the network model, the waveform of “LFP” oscillations can be determined through simulations. Since not all oscillation cycles are identical, the limit cycle waveform is averaged over 100 different cycles –as for the determination of – to yield an average limit cycle . Then, it is possible to evaluate a functional , where:(6)The functional is plotted in Figure 6B (right) for the used perturbation strength . Although Eq. (1) does not exactly hold for the network model, the top-down zero-crossings of the functional (whose position only weakly depends on ) continue to provide an approximation of the phase shifts between the two areas and in stable phase-locked states. In particular it is possible to predict whether the stable lockings will be in-phase, anti-phase or out-of-phase.

### Phase intervals for effective connectivity switching

Phase intervals in which the application of a pulsed perturbation leads to a change of effective connectivity directionality are determined theoretically as shown below. For and in a given phase-locking state, the phase of the leader area can be written as and the phase of the laggard area as . The application of a pulse perturbation of strength to the laggard area shifts the phase of the ongoing local oscillation to , where holds for the rate model in the case of small perturbations. If the achieved transient phase-shift between the two areas, , is falling into the basin of attraction of an alternative stable phase-locking (see Figure 6C), then a switching toward a different effective motif takes place. Considering the dynamics of the instantaneous phase-shift, determined by the functionals for the rate model and for the network model (see Figure 6B), switching will occur when:(7)Here, we consider perturbations which induce a phase advancement, because the positive part of both the PRC in the rate model and the empiric in the network model is larger than the negative part (see Figure 6D). For a fixed perturbation intensity , the condition (7) will be fulfilled only if when the phase of application of the perturbation falls within specific intervals, determined by the precise form of . These intervals are highlighted in green in Figure 6E and F. Analogous considerations can be done in order to determine the intervals for successful switching when perturbing the leader area (see Supporting Figure S2).

### Transfer Entropy (TE)

Let us consider first a structural motif with areas. Let and be the “LFP” time-series of the two areas and , and let quantize them into discrete levels (bins are equally sized). The continuous-valued “LFP” time-series are thus converted into strings of symbols and from a small alphabet [101]. Two transition probability matrices, and , where the lag is an arbitrary temporal scale on which causal interactions are probed, are then sampled as normalized multi-dimensional histograms over very long symbolic sequences. These probabilities are sampled separately for each specific fixed phase-locking configuration. Epochs in which the system switches to a different phase-locking configuration, as well as transients following state switchings are dropped. The evaluation of and is thus based on disconnected symbolic subsequences, including overall oscillation cycles. Then, following [42], the causal influence of area on area is defined as the Transfer Entropy:(8)where the sum runs over all the three indices , and of the transition matrices.

This quantity represents the Kullback-Leibler divergence [44] between the transition matrices and , analogous to a distance between probability distributions. Therefore, will vanish if and only if and coincide, i.e. if the transition probabilities between different “LFP” values of area do not depend on past “LFP” values of area . Conversely, this quantity will be strictly positive if these two transition matrices differ, i.e. if the past “LFP” values of area affect the evolution of the “LFP” in area .

We also measure the causal unbalancing [93]:(9)which is normalized in the range . A value close to zero denotes symmetric causal influences in the two directions, while large absolute values of signal the emergence of asymmetric effective connectivity motifs.

### Partialized Transfer Entropy (pTE)

Considering now a structural motif with areas, equation (8) has to be modified in order to distinguish causal interactions which are direct (e.g. toward ) from interactions which are indirect (e.g. toward , but through ). A solution allowing to assess only direct causal influences is partialization [42], [71]. Indirect interactions from area to area involving a third intermediate area are filtered out by conditioning the transition matrices for the “LFP” activity of with resepect to the activity of the . Two conditional transition matrices, and , are then constructed and used to evaluate:(10)where the sum runs over all the four indices , , and . The effective connectivity in the panels C of Figures 3, 4 and 5 is computed using pTE according to equation (10).

### Statistic validation of effective connectivity

Absolute values of depend strongly on the time-lag and on the number of discrete levels . Nevertheless, we find that relative strengths of causal influences are qualitatively unchanged over broad ranges of parameters, as displayed in the Supporting Figure S1. Furthermore the “plug-in” estimates of TE given by equations (8) and (10) suffer from finite-sampling biases, and a rigorous debiasing procedure is not yet known [43]. Therefore, for each value of and it is necessary to assess the significancy of the inferred causal interactions through comparison with suitably randomly resampled data [119]. To estimate the confidence intervals for the estimated TEs and the baseline for significancy we adopt a geometric bootstrap method [120], guaranteed to generate resampled time-series with similar auto- and cross-correlation properties up to a certain lag. This is important, since “LFP” time-series have a strong oscillatory component, whose correlation structure has to be maintained under resampling. Each resampled time-series consists of a concatenation of blocks sampled from the original time-series . Each has the same length as the original . Every upward crossing, i.e. every time at which crosses from below its time-averaged value , is a potential start-time for a block. The first element of each block is obtained by selecting randomly one of these potential start-times. Then, the block consists of the oscillation cycles following the chosen start-time, where the random integer follows a geometric distribution , with and an average block length of (we have taken oscillation cycles, longer than the mean correlation time for all the simulated “LFPs”). Randomly selected blocks are then concatenated up to the desired length.

When considering a structural motif involving more areas, the “LFP” time-series of each area can be resampled jointly or independently. When resampling jointly, matching starting points and block-lengths are selected for each block of the resampled time-series of each area, leading to resampled multivariate time-series in which the structure of causal influences should not be altered. The distribution of over jointly resampled “LFP” time-series describes then for each directed pair of areas and the strength of the corresponding effective connectivity link, as well as the fluctuations of this strength. Conversely, when resampling independently the time-series, start-points and block-lengths of the resampled blocks are chosen independently for each area. This second procedure leads by construction to causally independent time-series. Any residual between directed pairs of independently resampled “LFPs” indicates therefore systematic biases, rather than actual causal influences. For each directed pairs of areas and , significance of the corresponding causal interaction can be assessed by comparing the bootstrapped distributions of and of . This comparison is performed in Figures 3, 4 and 5 and in Supporting Figure S3D–E. Here, boxes indicate the median strength of for different directions and the corresponding confidence intervals, comprised between a lower extreme and and upper extreme , where and are respectively the first, the second and the third quartiles of the distribution of over jointly resampled time-series. Median values of and the corresponding confidence intervals, evaluated as before, are represented by horizontal dashed lines and a surrounding shaded band. When the distributions of and are not significantly different, a single baseline band is plotted. In this study, strengths and base-line for significancy of effective connectivity for each direction are validated based on, respectively, 500 jointly resampled and 500 independently resampled replicas.

Note that geometric bootstrap can be applied to arbitrary signals, and does not depend on their strict periodicity. However it is precisely the strong periodic component of our signals that makes necessary the use of geometric bootstrap techniques. Indeed, conventional bootstrap, strongly disrupting signal periodicity, would lead to artificially low thresholds for statistical significance of TE (not shown).

### Entropy and Mutual Information (MI)

We evaluate information transmission between pairs of mono-synaptically connected cells in different areas, linked by a TL-synapse (TL pairs) or by a normally weak long-range synapse (control pairs). Inspired by [58], spike trains are digitized into binary streams , where = 1 or 0 respectively when neuron fires or does not fire during the -th local oscillation cycle (cycle counting is performed independently for each area and includes all the oscillation cycles following a common reference initial time). Note that neurons fire very sparsely and, due to the elevated degree of synchrony in our model, only in narrow temporal intervals centered around the peaks of the ongoing “LFP” oscillations. In particular, they fire at maximum once per oscillation cycle. Thus, this oscillatory spiking activity is naturally quantized in time and binning [58] is not required. For each considered directed pair of cells ( source cell, target cell), based on very long duration spike trains, we sample normalized histograms for three probability distributions: , and . When sampling the joint probability distribution we have to distinguish two cases: (i) If the presynaptic cell belongs to a leader area, i.e. the oscillation of the source area leads in phase over the oscillation of the target area of the considered synapse, then ; (ii) Conversely, if the presynaptic cell belongs to a laggard area, i.e. the oscillation of the target area leads in phase over the oscillation of the source area of the considered synapse, then . This means that we seek for spiking correlations only in pairs of spiking (or missed spiking) events in which the “effect” follows temporally its potential “cause”, since physical information transmission cannot occur backward in time. As for the estimation of TE (see previous section), the probabilities , and are sampled separately for each specific phase-locking configuration of the ongoing “LFPs”. Epochs in which the system switches to a different phase-locking configuration, as well as transients following state switchings are dropped. The evaluation of these probabilities is thus based on disconnected spike train chunks, including overall oscillation cycles. Based on these probabilities, the Shannon entropy H of the spike train of the presynaptic neuron (measuring the information content in its activity) is evaluated as:(11)and MI between pre- and postsynaptic cells as:(12)MI is then normalized by the entropy of the pre-synaptic cell, in order to measure the relative efficiency of information transmission along each TL or control synapse.

Statistics are taken over 400 pairs of cells per synapse set, i.e. one set of strong synapses per embedded TL, plus one set of (control) weak synapses. The box-plots in Figure 8C–D report median efficiencies of information transmission efficiencies (for different active effective connectivities), as well as their confidence intervals, estimated non-parametrically from distribution quartiles, as discussed above for TE. Both MI and H are computed for (finite) spike trains of the largest available length . Following [58], [121], it is possible to correct these results for finite-size sampling bias (see Supporting Figure S4). MI and H are computed again, based on randomly selected shorter matching sections of the full length spike trains. The results of obtained for various shorter lengths are then plotted against the so-called inverse data fraction , where correspond then to estimations based on full length spike trains. Quadratic extrapolation to provides a debiased estimation of . Note that, in order to allow a more direct comparison with the non-debiased TE analysis, the results plotted in Figure 8C–D do not include any finite-size correction. As a matter of fact, as discussed in Supporting Figure S4, finite size bias induces a small quantitative overestimation of information transmission efficiency (from to ), that does not affect qualitatively any of the results presented here.

## Supporting Information

### Figure S1.

**Phase reduction and phase response.** A: oscillating time-series (in the example, a “LFP” time-series from the network model) can be described in terms of phase, even if they are not periodic in strict sense, by interpolating linearly an instantaneous empiric phase variable to the oscillation cycles (generally of unequal lengths). B: the application of a pulse current induces a shift in the oscillation phase of the ongoing oscillation (in the example, a rate trace from the rate model). The amplitude of the induced shift depends on the phase of the ongoing oscillation at which the perturbation is applied.

https://doi.org/10.1371/journal.pcbi.1002438.s001

(TIFF)

### Figure S2.

**Dynamic control of effective connectivity (perturbation applied to the leader area).** A–B: frequency histogram of successful switching for pulses applied at different phases ( for the rate model and for the network model). Predicted intervals for successful switching are marked in green, for the unidirectional (panel E) and for the leaky effective driving (panel F) motifs (left, rate model; right, network model; parameters as in Figures 3 and 4). Diagrams of the induced transitions are shown in the third column (see Figure 6 for perturbations applied to the laggard area).

https://doi.org/10.1371/journal.pcbi.1002438.s002

(TIFF)

### Figure S3.

**Effective connectivity with transmission lines (TLs).** We consider a fully symmetric structural motif of structurally connected areas with embedded unidirectional TLs. Synapses involved in TLs are enhanced by multiplying the ordinary excitatory peak conductance by a multiplier . Raster plots relative to the spiking activity of excitatory neurons of the two areas are shown in panels A–C (green and orange color denote spikes of excitatory neurons from different populations, the horizontal scale line corresponds to ) for a weak inter-areal coupling (unidirectional driving effective motif, see Figure 3 for parameters). A: when (no TL embedded), the synchronous oscillations of the two populations lock in an out-of-phase fashion. B: for (just below a critical value), the raster plot of the spiking activity is virtually indistinguishable from the raster plot of panel A. C: for (just above a critical value), the oscillations of the two populations lock in an in-phase configuration. D–E: Effective connectivities associated to different dynamical states are measured by Transfer Entropy (TE), evaluated from “LFPs” time-series, for all possible directed interactions (indicated by green or orange arrows). Boxes indicate the interquartile range and whiskers the confidence interval for the estimated TEs. TEs above the grey horizontal band indicate statistically significant causal influences (see *Methods*). In each plot, the third and the fourth boxes (from left to right) refer to TEs evaluated from “LFPs” restricted to groups of neurons that are source and target of a TL (pale green color denotes TL in the “green-to-orange” area direction, lilac color denotes TL in the “orange-to-green” area direction). Below each TE box-plot, effective connectivity is also represented in a diagrammatic form. Arrow thicknesses encode the strength of corresponding causal interactions (if statistically significant). D: TEs for the unidirectional driving effective motif with embedded TLs (). E: TEs for the leaky driving effective motif with embedded TLs (). Comparing these effective motifs with Figures 3 and 4, we conclude that the embedding of TLs does not alter the overall effective connectivity.

https://doi.org/10.1371/journal.pcbi.1002438.s003

(TIFF)

### Figure S4.

**Scaling of Mutual Information (MI) with spike train length.** MI normalized by entropy (at optimal time lag) is plotted against the inverse data fraction . For each data fraction , several bivariate spike trains are extracted from the original long spike trains (, ) and the mean MI is further averaged over these reduced-length spike trains. Asymptotic values are extrapolated through a quadratic interpolation. Error bars correspond to standard error. A: unidirectional driving effective motif, MI along the TL in the leader-to-laggard direction (pale green color), extrapolated asymptotic value is . B: unidirectional driving effective motif, MI along the TL in the laggard-to-leader direction (lilac color), extrapolated asymptotic value is . In both cases, the finite size of the used spike trains produces a positive but small bias in the estimation of MI. Compared to Figure 8C, for the leader-to-laggard direction the overestimation is of and for the laggard-to-leader direction is of .

https://doi.org/10.1371/journal.pcbi.1002438.s004

(TIFF)

### Text S1.

**Full description of model parameters and complete analytic expressions.** This text contains the following sections: i) Model neurons; ii) Model synapses; iii) Parameters of the background noise; iv) Phase response of the rate model; v) Phase-locking in the rate model.

https://doi.org/10.1371/journal.pcbi.1002438.s005

(PDF)

## Acknowledgments

We thank Albert Compte for useful suggestions and Olav Stetter for figure editing. DB wishes to credit Nicolas Brunel and David Hansel for earlier collaboration on the models used in this study.

## Author Contributions

Wrote the paper: DB AW FW TG. Conceived and designed the models: DB FW TG. Contributed statistical tools: AW. Performed simulations: DB. Analyzed simulation results: DB AW.

## References

- 1. Fairhall SL, Ishai A (2007) Effective Connectivity within the Distributed Cortical Network for Face Perception. Cereb Cort 17: 2400–2406.SL FairhallA. Ishai2007Effective Connectivity within the Distributed Cortical Network for Face Perception.Cereb Cort1724002406
- 2. Steeves JK, Culham JC, Duchaine BC, Pratesi CC, Valyear KF, et al. (2006) The fusiform face area is not sufficient for face recognition: Evidence from a patient with dense prosopagnosia and no occipital face area. Neuropsychol 44: 594–609.JK SteevesJC CulhamBC DuchaineCC PratesiKF Valyear2006The fusiform face area is not sufficient for face recognition: Evidence from a patient with dense prosopagnosia and no occipital face area.Neuropsychol44594609
- 3. Vuilleumier P, Driver J (2007) Modulation of visual processing by attention and emotion: windows on causal interactions between human brain regions. Phil Trans R Soc B 362: 837–855.P. VuilleumierJ. Driver2007Modulation of visual processing by attention and emotion: windows on causal interactions between human brain regions.Phil Trans R Soc B362837855
- 4. Brovelli A, Ding M, Ledberg A, Chen Y, Nakamura R, et al. (2004) Beta oscillations in a large-scale sensorimotor cortical network: Directional influences revealed by Granger causality. Proc Natl Acad Sci USA 101: 9849–9854.A. BrovelliM. DingA. LedbergY. ChenR. Nakamura2004Beta oscillations in a large-scale sensorimotor cortical network: Directional influences revealed by Granger causality.Proc Natl Acad Sci USA10198499854
- 5. Clapp WC, Rubens MT, Sabharwal J, Gazzaley A (2011) Deficit in switching between functional brain networks underlies the impact of multitasking on working memory in older adults. Proc Natl Acad Sci USA 108: 7212–7217.WC ClappMT RubensJ. SabharwalA. Gazzaley2011Deficit in switching between functional brain networks underlies the impact of multitasking on working memory in older adults.Proc Natl Acad Sci USA10872127217
- 6. Rossi AF, Pessoa L, Desimone R, Ungerleider LG (2009) The prefrontal cortex and the executive control of attention. Exp Brain Res 192: 489–497.AF RossiL. PessoaR. DesimoneLG Ungerleider2009The prefrontal cortex and the executive control of attention.Exp Brain Res192489497
- 7. Corbetta M, Shulman GL (2002) Control of goal-directed and stimulus-driven attention in the brain. Nat Rev Neurosci 3: 201–215.M. CorbettaGL Shulman2002Control of goal-directed and stimulus-driven attention in the brain.Nat Rev Neurosci3201215
- 8. Zanto TP, Rubens MT, Thangavel A, Gazzaley A (2011) Causal role of the prefrontal cortex in top-down modulation of visual processing and working memory. Nat Neurosci 14: 656–661.TP ZantoMT RubensA. ThangavelA. Gazzaley2011Causal role of the prefrontal cortex in top-down modulation of visual processing and working memory.Nat Neurosci14656661
- 9. Gaillard R, Dehaene S, Adam C, Clémenceau S, Hasboun D, et al. (2009) Converging intracranial markers of conscious access. PLoS Biol 7: 472–492.R. GaillardS. DehaeneC. AdamS. ClémenceauD. Hasboun2009Converging intracranial markers of conscious access.PLoS Biol7472492
- 10. Tononi G, Edelman GM, Sporns O (1998) Complexity and coherency: integrating information in the brain. Trends Cogn Sci 2: 474–84.G. TononiGM EdelmanO. Sporns1998Complexity and coherency: integrating information in the brain.Trends Cogn Sci247484
- 11. Bressler SL, Kelso JA (2001) Cortical coordination dynamics and cognition. Trends Cogn Sci 5: 26–36.SL BresslerJA Kelso2001Cortical coordination dynamics and cognition.Trends Cogn Sci52636
- 12. Varela F, Lachaux JP, Rodriguez E, Martinerie J (2001) The brainweb: Phase synchronization and large-scale integration. Nat Rev Neurosci 2: 229–239.F. VarelaJP LachauxE. RodriguezJ. Martinerie2001The brainweb: Phase synchronization and large-scale integration.Nat Rev Neurosci2229239
- 13. Friston KJ (1994) Functional and effective connectivity: a synthesis. Hum Brain Mapp 2: 56–78.KJ Friston1994Functional and effective connectivity: a synthesis.Hum Brain Mapp25678
- 14. Ioannides AA (2007) Dynamic functional connectivity. Curr Opin Neurobiol 17: 161–70.AA Ioannides2007Dynamic functional connectivity.Curr Opin Neurobiol1716170
- 15. Friston KJ (2011) Functional and effective connectivity: a review. Brain Conn 1: 13–36.KJ Friston2011Functional and effective connectivity: a review.Brain Conn11336
- 16. Bressler SL, Seth AK (2011) Wiener-Granger Causality: A well established methodology. NeuroImage 58: 323–329.SL BresslerAK Seth2011Wiener-Granger Causality: A well established methodology.NeuroImage58323329
- 17. Gilbert CD, Sigman M (2007) Brain states: top-down influences in sensory processing. Neuron 54: 677–696.CD GilbertM. Sigman2007Brain states: top-down influences in sensory processing.Neuron54677696
- 18. Haken H, Kelso JA, Bunz H (1985) A theoretical model of phase transitions in human hand movements. Biol Cybern 51: 347–56.H. HakenJA KelsoH. Bunz1985A theoretical model of phase transitions in human hand movements.Biol Cybern5134756
- 19. Ditzinger T, Haken H (1989) Oscillations in the perception of ambiguous patterns: a model based on synergetics. Biol Cybern 61: 279–287.T. DitzingerH. Haken1989Oscillations in the perception of ambiguous patterns: a model based on synergetics.Biol Cybern61279287
- 20. Lumer ED, Friston KJ, Rees G (1998) Neural correlates of perceptual rivalry in the human brain. Science 280: 1930–1934.ED LumerKJ FristonG. Rees1998Neural correlates of perceptual rivalry in the human brain.Science28019301934
- 21. Deco G, Scarano L, Soto-Faraco S (2007) Weber's law in decision making: integrating behavioral data in humans with a neurophysiological model. J Neurosci 27: 11192–200.G. DecoL. ScaranoS. Soto-Faraco2007Weber's law in decision making: integrating behavioral data in humans with a neurophysiological model.J Neurosci2711192200
- 22. Moreno-Bote R, Rinzel J, Rubin N (2007) Noise-induced alternations in an attractor network model of perceptual bistability. J Neurophysiol 98: 1125–39.R. Moreno-BoteJ. RinzelN. Rubin2007Noise-induced alternations in an attractor network model of perceptual bistability.J Neurophysiol98112539
- 23. Misic B, Mills T, Taylor MJ, McIntosh AR (2010) Brain Noise Is Task Dependent and Region Specific. J Neurophysiol 104: 2667–2676.B. MisicT. MillsMJ TaylorAR McIntosh2010Brain Noise Is Task Dependent and Region Specific.J Neurophysiol10426672676
- 24. Deco G, Romo R (2008) The role of fluctuations in perception. Trends Neurosci 31: 591–8.G. DecoR. Romo2008The role of fluctuations in perception.Trends Neurosci315918
- 25. Deco G, Rolls ET, Romo R (2009) Stochastic dynamics as a principle of brain function. Prog Neurobiol 88: 1–16.G. DecoET RollsR. Romo2009Stochastic dynamics as a principle of brain function.Prog Neurobiol88116
- 26. Deco G, Jirsa VK, McIntosh R (2011) Emerging concepts for the dynamical organization of resting-state activity in the brain. Nat Rev Neurosci 12: 43–56.G. DecoVK JirsaR. McIntosh2011Emerging concepts for the dynamical organization of resting-state activity in the brain.Nat Rev Neurosci124356
- 27. Freyer F, Aquino K, Robinson PA, Ritter P, Breakspear M (2009) Bistability and non-Gaussian fluctuations in spontaneous cortical activity. J Neurosci 29: 8512–8524.F. FreyerK. AquinoPA RobinsonP. RitterM. Breakspear2009Bistability and non-Gaussian fluctuations in spontaneous cortical activity.J Neurosci2985128524
- 28. Freyer F, Roberts JA, Becker R, Robinson PA, Ritter P, et al. (2011) Biophysical mechanisms of multistability in resting-state cortical rhythms. J Neurosci 31: 6353–6361.F. FreyerJA RobertsR. BeckerPA RobinsonP. Ritter2011Biophysical mechanisms of multistability in resting-state cortical rhythms.J Neurosci3163536361
- 29. Wang XJ (2010) Neurophysiological and computational principles of cortical rhythms in cognition. Physiol Rev 90: 1195–1268.XJ Wang2010Neurophysiological and computational principles of cortical rhythms in cognition.Physiol Rev9011951268
- 30. Engel A, Fries P, Singer W (2001) Dynamic predictions: oscillations and synchrony in top-down processing. Nat Rev Neurosci 2: 704–716.A. EngelP. FriesW. Singer2001Dynamic predictions: oscillations and synchrony in top-down processing.Nat Rev Neurosci2704716
- 31. Fries P (2005) A mechanism for cognitive dynamics: neuronal communication through neuronal coherence. Trends Cogn Sci 9: 474–480.P. Fries2005A mechanism for cognitive dynamics: neuronal communication through neuronal coherence.Trends Cogn Sci9474480
- 32. Fries P, Nikolić D, Singer W (2007) The gamma cycle. Trends Neurosci 30: 309–16.P. FriesD. NikolićW. Singer2007The gamma cycle.Trends Neurosci3030916
- 33. Volgushev M, Chistiakova M, Singer W (1998) Modification of discharge patterns of neocortical neurons by induced oscillations of the membrane potential. Neuroscience 83: 15–25.M. VolgushevM. ChistiakovaW. Singer1998Modification of discharge patterns of neocortical neurons by induced oscillations of the membrane potential.Neuroscience831525
- 34. Schoffelen JM, Oostenveld R, Fries P (2005) Neuronal coherence as a mechanism of effective corticospinal interaction. Science 308: 111–3.JM SchoffelenR. OostenveldP. Fries2005Neuronal coherence as a mechanism of effective corticospinal interaction.Science3081113
- 35. Womelsdorf T, Schoffelen JM, Oostenveld R, SingerW , Desimone R, et al. (2007) Modulation of neuronal interactions through neuronal synchronization. Science 316: 1609–1612.T. WomelsdorfJM SchoffelenR. OostenveldSingerWR. Desimone2007Modulation of neuronal interactions through neuronal synchronization.Science31616091612
- 36. Ghazanfar AA, Chandrasekaran C, Logothetis NK (2008) Interactions between the Superior temporal sulcus and Auditory cortex mediate dynamic face/voice integration in rhesus monkeys. J Neurosci 28: 4457–4469.AA GhazanfarC. ChandrasekaranNK Logothetis2008Interactions between the Superior temporal sulcus and Auditory cortex mediate dynamic face/voice integration in rhesus monkeys.J Neurosci2844574469
- 37. Canolty RT, Ganguly K, Kennerley SW, Cadieu CF, Koepsell K, et al. (2010) Oscillatory phase coupling coordinates anatomically dispersed functional cell assemblies. Proc Natl Acad Sci U S A 107: 17356–61.RT CanoltyK. GangulySW KennerleyCF CadieuK. Koepsell2010Oscillatory phase coupling coordinates anatomically dispersed functional cell assemblies.Proc Natl Acad Sci U S A1071735661
- 38. Hipp JF, Engel AK, Siegel M (2011) Oscillatory synchronization in large-scale cortical networks predicts perception. Neuron 69: 387–396.JF HippAK EngelM. Siegel2011Oscillatory synchronization in large-scale cortical networks predicts perception.Neuron69387396
- 39. Fries P, Womelsdorf T, Oostenveld R, Desimone R (2008) The effects of visual stimulation and selective visual attention on rhythmic neuronal synchronization in macaque area V4. J Neurosci 28: 4823–4835.P. FriesT. WomelsdorfR. OostenveldR. Desimone2008The effects of visual stimulation and selective visual attention on rhythmic neuronal synchronization in macaque area V4.J Neurosci2848234835
- 40. Gregoriou GG, Gotts SJ, Zhou H, Desimone R (2009) High-frequency, long-range coupling between prefrontal and visual cortex during attention. Science 324: 1207–1210.GG GregoriouSJ GottsH. ZhouR. Desimone2009High-frequency, long-range coupling between prefrontal and visual cortex during attention.Science32412071210
- 41. Honey CJ, Kötter R, Breakspear M, Sporns O (2007) Network structure of cerebral cortex shapes functional connectivity on multiple time scales. Proc Natl Acad Sci USA 104: 10240–10245.CJ HoneyR. KötterM. BreakspearO. Sporns2007Network structure of cerebral cortex shapes functional connectivity on multiple time scales.Proc Natl Acad Sci USA1041024010245
- 42. Schreiber T (2000) Measuring information transfer. Phys Rev Lett 85: 461–464.T. Schreiber2000Measuring information transfer.Phys Rev Lett85461464
- 43. Kaiser A, Schreiber T (2002) Information transfer in continuous processes. Physica D 166: 43–62.A. KaiserT. Schreiber2002Information transfer in continuous processes.Physica D1664362
- 44.
MacKay D (2003) Information theory, inference, and learning algorithms. Cambridge: Cambridge University Press. 640 p.D. MacKay2003Information theory, inference, and learning algorithmsCambridgeCambridge University Press640
- 45. Granger CWJ (1969) Investigating causal relations by econometric models and crossspectral methods. Econometrica 37: 424–438.CWJ Granger1969Investigating causal relations by econometric models and crossspectral methods.Econometrica37424438
- 46.
Ding M, Chen Y, Bressler SL (2006) Granger causality: Basic theory and application to neuroscience. In: Schelter S, Winterhalder N, Timmer J, editors. Handbook of Time Series Analysis. Wienheim: Wiley. pp. 437–460.M. DingY. ChenSL Bressler2006Granger causality: Basic theory and application to neuroscience.S. SchelterN. WinterhalderJ. TimmerHandbook of Time Series AnalysisWienheimWiley437460
- 47.
Kuramoto Y (1984) Chemical Oscillations, Waves, and Turbulence. New York: Springer. 164 p.Y. Kuramoto1984Chemical Oscillations, Waves, and TurbulenceNew YorkSpringer164
- 48. Constantinople CM, Bruno RM (2011) Effects and mechanisms of wakefulness on local cortical networks. Neuron 69: 1061–1068.CM ConstantinopleRM Bruno2011Effects and mechanisms of wakefulness on local cortical networks.Neuron6910611068
- 49. MacKay D, McCulloch WS (1952) The limiting information capacity of a neuronal link. Bull Math Biophys 14: 127–135.D. MacKayWS McCulloch1952The limiting information capacity of a neuronal link.Bull Math Biophys14127135
- 50. Mainen ZF, Sejnowsky TJ (1995) Reliability of spike timing in neocortical neurons. Science 268: 1503–1506.ZF MainenTJ Sejnowsky1995Reliability of spike timing in neocortical neurons.Science26815031506
- 51. Reich DS, Mechler F, Victor JD (2001) Independent and redundant information in nearby cortical neurons. Science 294: 2566–2558.DS ReichF. MechlerJD Victor2001Independent and redundant information in nearby cortical neurons.Science29425662558
- 52. Osborne LC, Palmer SE, Lisberger SG, Bialek W (2008) The neural basis for combinatorial coding in a cortical population response. J Neurosci 28: 13522–13531.LC OsborneSE PalmerSG LisbergerW. Bialek2008The neural basis for combinatorial coding in a cortical population response.J Neurosci281352213531
- 53. Ohiorhenuan IE, Mechler F, Purpura KP, Schmid AM, Hu Q, et al. (2010) Sparse coding and high-order correlations in fine-scale cortical networks. Nature 466: 617–621.IE OhiorhenuanF. MechlerKP PurpuraAM SchmidQ. Hu2010Sparse coding and high-order correlations in fine-scale cortical networks.Nature466617621
- 54. Brunel N, Hakim V (1999) Fast global oscillations in networks of integrate-and-fire neurons with low firing rates. Neural Comput 11: 1621–1671.N. BrunelV. Hakim1999Fast global oscillations in networks of integrate-and-fire neurons with low firing rates.Neural Comput1116211671
- 55. Brunel N, Wang XJ (2003) What determines the frequency of fast network oscillations with irregular neural discharges? J Neurophysiol 90: 415–430.N. BrunelXJ Wang2003What determines the frequency of fast network oscillations with irregular neural discharges?J Neurophysiol90415430
- 56. Brunel N, Hansel D (2006) How noise affects the synchronization properties of recurrent networks of inhibitory neurons. Neural Comput 18: 1066–1110.N. BrunelD. Hansel2006How noise affects the synchronization properties of recurrent networks of inhibitory neurons.Neural Comput1810661110
- 57. Brunel N, Hakim V (2008) Sparsely synchronized neuronal oscillations. Chaos 18: 015113.N. BrunelV. Hakim2008Sparsely synchronized neuronal oscillations.Chaos18015113
- 58. Strong SP, Koberle R, de Ruyter van Steveninck RR, Bialek W (1998) Entropy and information in neural spike trains. Phys Rev Lett 80: 197–200.SP StrongR. KoberleRR de Ruyter van SteveninckW. Bialek1998Entropy and information in neural spike trains.Phys Rev Lett80197200
- 59. Roskies A, editor. (1999) The binding problem: special issue. Neuron 24: 7–125.A. Roskies1999The binding problem: special issue.Neuron247125
- 60. Battaglia D, Brunel N, Hansel D (2007) Temporal decorrelation of collective oscillations in neural networks with local inhibition and long-range excitation. Phys Rev Lett 99: 238106–10.D. BattagliaN. BrunelD. Hansel2007Temporal decorrelation of collective oscillations in neural networks with local inhibition and long-range excitation.Phys Rev Lett9923810610
- 61. Bartos M, Vida I, Jonas P (2007) Synaptic mechanisms of synchronized gamma oscillations in inhibitory interneuron networks. Nature Rev Neurosci 8: 45–56.M. BartosI. VidaP. Jonas2007Synaptic mechanisms of synchronized gamma oscillations in inhibitory interneuron networks.Nature Rev Neurosci84556
- 62. Cardin JA, Carln M, Meletis K, Knoblich U, Zhang F, et al. (2009) Driving fast-spiking cells induces gamma rhythm and controls sensory responses. Nature 459: 663–667.JA CardinM. CarlnK. MeletisU. KnoblichF. Zhang2009Driving fast-spiking cells induces gamma rhythm and controls sensory responses.Nature459663667
- 63. Whittington MA, Traub RD, Jefferys JG (1995) Synchronized oscillations in interneuron networks driven by metabotropic glutamate receptor activation. Nature 373: 612–615.MA WhittingtonRD TraubJG Jefferys1995Synchronized oscillations in interneuron networks driven by metabotropic glutamate receptor activation.Nature373612615
- 64. Sporns O, Kötter R (2004) Motifs in brain networks. PLoS Biol 2: e369.O. SpornsR. Kötter2004Motifs in brain networks.PLoS Biol2e369
- 65. Breakspear M, Jirsa V, Deco G (2010) Computational models of the brain: from structure to function. Neuroimage 52: 727–730.M. BreakspearV. JirsaG. Deco2010Computational models of the brain: from structure to function.Neuroimage52727730
- 66. Seth AK (2005) Causal connectivity analysis of evolved neural networks during behavior. Network 16: 35–55.AK Seth2005Causal connectivity analysis of evolved neural networks during behavior.Network163555
- 67. Landau LD (1937) On the theory of phase transitions. Physikalische Zeitschrift der Sowjetunion 11: 26–47.LD Landau1937On the theory of phase transitions.Physikalische Zeitschrift der Sowjetunion112647
- 68.
Schuster HG, Just W (2005) Deterministic chaos. Weinheim: Wiley. 287 p.HG SchusterW. Just2005Deterministic chaosWeinheimWiley287
- 69. Battaglia D, Hansel D (2011) Synchronous chaos and broad band gamma rhythm in a minimal multi-layer model of primary visual cortex. PLoS Comput Biol 7: e1002176.D. BattagliaD. Hansel2011Synchronous chaos and broad band gamma rhythm in a minimal multi-layer model of primary visual cortex.PLoS Comput Biol7e1002176
- 70.
Pikovsky A, Rosenblum M, Kurths J (2001) Synchronization: a universal concept in nonlinear sciences. Cambridge: Cambridge University Press. 432 p.A. PikovskyM. RosenblumJ. Kurths2001Synchronization: a universal concept in nonlinear sciencesCambridgeCambridge University Press432
- 71. Barnett L, Barrett AB, Seth AK (2009) Granger causality and transfer entropy are equivalent for gaussian variables. Phys Rev Lett 103: 238701–5.L. BarnettAB BarrettAK Seth2009Granger causality and transfer entropy are equivalent for gaussian variables.Phys Rev Lett1032387015
- 72. Dan Y, Poo M (2004) Spike timing-dependent plasticity of neural circuits. Neuron 44: 23–30.Y. DanM. Poo2004Spike timing-dependent plasticity of neural circuits.Neuron442330
- 73. Song S, Sjöström PJ, Reigl M, Nelson S, Chklovskii DB (2005) Highly nonrandom features of synaptic connectivity in local cortical circuits. PLoS Biol 3: e68.S. SongPJ SjöströmM. ReiglS. NelsonDB Chklovskii2005Highly nonrandom features of synaptic connectivity in local cortical circuits.PLoS Biol3e68
- 74. Brunel N, Wang XJ (2001) Effects of neuromodulation in a cortical network model of object working memory dominated by recurrent inhibition. J Comput Neurosci 11: 63–85.N. BrunelXJ Wang2001Effects of neuromodulation in a cortical network model of object working memory dominated by recurrent inhibition.J Comput Neurosci116385
- 75. Seamans JK, Yang CR (2004) The principal features and mechanisms of dopamine modulation in the prefrontal cortex. Prog Neurobiol 74: 1–58.JK SeamansCR Yang2004The principal features and mechanisms of dopamine modulation in the prefrontal cortex.Prog Neurobiol74158
- 76. O' Keefe J, Recce ML (1993) Phase relationship between hippocampal place units and the EEG theta rhythm. Hippocampus 3: 317–330.J. O' KeefeML Recce1993Phase relationship between hippocampal place units and the EEG theta rhythm.Hippocampus3317330
- 77. Laurent G, Davidowitz H (1994) Encoding of olfactory information with oscillating neural assemblies. Science 265: 1872–1875.G. LaurentH. Davidowitz1994Encoding of olfactory information with oscillating neural assemblies.Science26518721875
- 78. Lisman J (2005) The theta/gamma discrete phase code occuring during the hippocampal phase precession may be a more general brain coding scheme. Hippocampus 15: 913–922.J. Lisman2005The theta/gamma discrete phase code occuring during the hippocampal phase precession may be a more general brain coding scheme.Hippocampus15913922
- 79. Montemurro MA, Rasch MJ, Murayama Y, Logothetis NK, Panzeri S (2008) Phase-offiring coding of natural visual stimuli in primary visual cortex. Curr Biol 18: 375–380.MA MontemurroMJ RaschY. MurayamaNK LogothetisS. Panzeri2008Phase-offiring coding of natural visual stimuli in primary visual cortex.Curr Biol18375380
- 80. Vinck M, Lima B, Womelsdorf T, Oostenveld R, Singer W, et al. (2010) Gamma-phase shifting in awake monkey visual cortex. J Neurosci 30: 1250–1257.M. VinckB. LimaT. WomelsdorfR. OostenveldW. Singer2010Gamma-phase shifting in awake monkey visual cortex.J Neurosci3012501257
- 81. Nadasdy Z (2010) Binding by asynchrony: the neuronal phase code. Front Neurosci 4: article 51.Z. Nadasdy2010Binding by asynchrony: the neuronal phase code.Front Neurosci4article 51
- 82. DeCharms RC, Merzenich MM (1996) Primary cortical representations of sounds by the coordination of action-potential timing. Nature 381: 610–613.RC DeCharmsMM Merzenich1996Primary cortical representations of sounds by the coordination of action-potential timing.Nature381610613
- 83. Arabzadeh E, Panzeri S, Diamond ME (2006) Deciphering the spike train of a sensory neuron: counts and temporal patterns in the rat whisker pathway. J Neurosci 26: 9216–9226.E. ArabzadehS. PanzeriME Diamond2006Deciphering the spike train of a sensory neuron: counts and temporal patterns in the rat whisker pathway.J Neurosci2692169226
- 84. Koepsell K, Wang X, Hirsch JA, Sommer FT (2010) Exploring the function of neural oscillations in early sensory systems. Front Neurosci 4: 53.K. KoepsellX. WangJA HirschFT Sommer2010Exploring the function of neural oscillations in early sensory systems.Front Neurosci453
- 85. Tiesinga P, Fellous JM, Sejnowski TJ (2008) Regulation of spike timing in visual cortical circuits. Nat Rev Neurosci 9: 97–107.P. TiesingaJM FellousTJ Sejnowski2008Regulation of spike timing in visual cortical circuits.Nat Rev Neurosci997107
- 86. Tiesinga PH, Sejnowski TJ (2010) Mechanisms for phase shifting in cortical networks and their role in communication through coherence. Front Hum Neurosci 4: 196.PH TiesingaTJ Sejnowski2010Mechanisms for phase shifting in cortical networks and their role in communication through coherence.Front Hum Neurosci4196
- 87. Kayser C, Logothetis NK, Panzeri S (2010) Millisecond encoding precision of auditory cortex neurons. Proc Natl Acad Sci USA 107: 16976–16981.C. KayserNK LogothetisS. Panzeri2010Millisecond encoding precision of auditory cortex neurons.Proc Natl Acad Sci USA1071697616981
- 88. Ghosh A, Rho Y, McIntosh AR, Ktter R, Jirsa VK (2008) Noise during rest enables the exploration of the brain's dynamic repertoire. PLoS Comp Biol 4: e1000196.A. GhoshY. RhoAR McIntoshR. KtterVK Jirsa2008Noise during rest enables the exploration of the brain's dynamic repertoire.PLoS Comp Biol4e1000196
- 89. Deco G, Jirsa V, McIntosh AR, Sporns O, Ktter R (2009) Key role of coupling, delay, and noise in resting brain fluctuations. Proc Natl Acad Sci USA 106: 10302–10307.G. DecoV. JirsaAR McIntoshO. SpornsR. Ktter2009Key role of coupling, delay, and noise in resting brain fluctuations.Proc Natl Acad Sci USA1061030210307
- 90. Friston KJ, Harrison L, Penny W (2003) Dynamic causal modelling. NeuroImage 19: 1273–1302.KJ FristonL. HarrisonW. Penny2003Dynamic causal modelling.NeuroImage1912731302
- 91. Valdes-Sosa P, Roebroeck A, Daunizeau J, Friston K (2011) Effective connectivity: Influence, causality and biophysical modeling. NeuroImage 58: 339–361.P. Valdes-SosaA. RoebroeckJ. DaunizeauK. Friston2011Effective connectivity: Influence, causality and biophysical modeling.NeuroImage58339361
- 92. Vicente R, Wibral M, Lindner M, Pipa G (2011) Transfer entropy — a model-free measure of effective connectivity for the neurosciences. J Comput Neurosci 30: 45–67.R. VicenteM. WibralM. LindnerG. Pipa2011Transfer entropy — a model-free measure of effective connectivity for the neurosciences.J Comput Neurosci304567
- 93. Gourévitch B, Eggermont JJ (2007) Evaluating information transfer between auditory cortical neurons. J Neurophysiol 97: 2533–2543.B. GourévitchJJ Eggermont2007Evaluating information transfer between auditory cortical neurons.J Neurophysiol9725332543
- 94. Besserve M, Schölkopf B, Logothetis NK, Panzeri S (2010) Causal relationships between frequency bands of extracellular signals in visual cortex revealed by an information theoretic analysis. J Comput Neurosci 29: 547–566.M. BesserveB. SchölkopfNK LogothetisS. Panzeri2010Causal relationships between frequency bands of extracellular signals in visual cortex revealed by an information theoretic analysis.J Comput Neurosci29547566
- 95. Wibral M, Rahm B, Rieder M, Lindner M, Vicente R, et al. (2011) Transfer entropy in magnetoencephalographic data: quantifying information flow in cortical and cerebellar networks. Prog Biophys Mol Biol 105: 80–97.M. WibralB. RahmM. RiederM. LindnerR. Vicente2011Transfer entropy in magnetoencephalographic data: quantifying information flow in cortical and cerebellar networks.Prog Biophys Mol Biol1058097
- 96. Gourévitch B, Bouquin-Jeannès RL, Faucon G (2006) Linear and nonlinear causality between signals: methods, examples and neurophysiological applications. Biol Cybern 95: 349–369.B. GourévitchRL Bouquin-JeannèsG. Faucon2006Linear and nonlinear causality between signals: methods, examples and neurophysiological applications.Biol Cybern95349369
- 97. Marinazzo D, Pellicoro M, Stramaglia S (2008) Kernel method for nonlinear granger causality. Phys Rev Lett 100: 144103.D. MarinazzoM. PellicoroS. Stramaglia2008Kernel method for nonlinear granger causality.Phys Rev Lett100144103
- 98. Stephan KE, Kasper L, Harrison LM, Daunizeau J, den Ouden HEM, et al. (2008) Nonlinear dynamic causal models for fMRI. NeuroImage 42: 649–662.KE StephanL. KasperLM HarrisonJ. DaunizeauHEM den Ouden2008Nonlinear dynamic causal models for fMRI.NeuroImage42649662
- 99. Marinazzo D, Liao W, Chen H, Stramaglia S (2011) Nonlinear connectivity by Granger causality. NeuroImage 58: 330–338.D. MarinazzoW. LiaoH. ChenS. Stramaglia2011Nonlinear connectivity by Granger causality.NeuroImage58330338
- 100.
Pearl J (2000) Causality: Models, Reasoning and Inference. Cambridge: Cambridge University Press. 464 p.J. Pearl2000Causality: Models, Reasoning and InferenceCambridgeCambridge University Press464
- 101. Staniek M, Lehnertz K (2008) Symbolic transfer entropy. Phys Rev Lett 100: 158101–5.M. StaniekK. Lehnertz2008Symbolic transfer entropy.Phys Rev Lett1001581015
- 102. Roelfsema PR, Engel AK, Koening P, Singer W (1997) Visuomotor integration is associated with zero-lag synchronization among cortical areas. Nature 385: 157–161.PR RoelfsemaAK EngelP. KoeningW. Singer1997Visuomotor integration is associated with zero-lag synchronization among cortical areas.Nature385157161
- 103. Westendorff S, Klaes C, Gail A (2010) The cortical timeline for deciding on reach motor goals. J Neurosci 30: 5426–5436.S. WestendorffC. KlaesA. Gail2010The cortical timeline for deciding on reach motor goals.J Neurosci3054265436
- 104. Mainy N, Jung J, Baciu M, Kahane P, Schoendorff B, et al. (2008) Cortical dynamics of word recognition. Hum Brain Mapp 29: 1215–1230.N. MainyJ. JungM. BaciuP. KahaneB. Schoendorff2008Cortical dynamics of word recognition.Hum Brain Mapp2912151230
- 105. Perin R, Berger TK, Markram H (2011) A synaptic organizing principle for cortical neuronal groups. Proc Natl Acad Sci USA 108: 5419–5424.R. PerinTK BergerH. Markram2011A synaptic organizing principle for cortical neuronal groups.Proc Natl Acad Sci USA10854195424
- 106. Aertsen AM, Gerstein GL, Habib MK, Palm G (1989) Dynamics of neuronal firing correlation: modulation of “effective connectivity”. J Neurophysiol 61: 900–917.AM AertsenGL GersteinMK HabibG. Palm1989Dynamics of neuronal firing correlation: modulation of “effective connectivity”.J Neurophysiol61900917
- 107. Kispersky T, Gutierrez GJ, Marder E (2011) Functional connectivity in a rhythmic inhibitory circuit using Granger causality. Neural Syst Circuits 1: 9.T. KisperskyGJ GutierrezE. Marder2011Functional connectivity in a rhythmic inhibitory circuit using Granger causality.Neural Syst Circuits19
- 108. Rolls ET, Treves A (2011) The neuronal encoding of information in the brain. Prog Neurobiol 95: 448–490.ET RollsA. Treves2011The neuronal encoding of information in the brain.Prog Neurobiol95448490
- 109. Jarvis MR, Mitra PP (2001) Sampling properties of the spectrum and coherency of sequences of action potentials. Neural Comput 13: 717–749.MR JarvisPP Mitra2001Sampling properties of the spectrum and coherency of sequences of action potentials.Neural Comput13717749
- 110. Murȩsan RC, Jurjuţ OF, Moca VV, Singer W, Nikolić D (2008) The oscillation score: an efficient method for estimating oscillation strength in neuronal activity. J Neurophysiol 99: 1333–1353.RC MurȩsanOF JurjuţVV MocaW. SingerD. Nikolić2008The oscillation score: an efficient method for estimating oscillation strength in neuronal activity.J Neurophysiol9913331353
- 111. Yu J, Ferster D (2010) Membrane potential synchrony in primary visual cortex during sensory stimulation. Neuron 68: 1187–1201.J. YuD. Ferster2010Membrane potential synchrony in primary visual cortex during sensory stimulation.Neuron6811871201
- 112. Buehlmann A, Deco G (2010) Optimal information transfer in the cortex through synchronization. PLoS Comput Biol 6(9): e1000934.A. BuehlmannG. Deco2010Optimal information transfer in the cortex through synchronization.PLoS Comput Biol69e1000934
- 113. Buffalo EA, Fries P, Landman R, Buschman TJ, Desimone R (2011) Laminar differences in gamma and alpha coherence in the ventral stream. Proc Natl Acad Sci USA 108: 11262–7.EA BuffaloP. FriesR. LandmanTJ BuschmanR. Desimone2011Laminar differences in gamma and alpha coherence in the ventral stream.Proc Natl Acad Sci USA108112627
- 114. Histed H, Bonin V, Reid RC (2009) Direct activation of sparse, distributed populations of cortical neurons by electrical microstimulation. Neuron 63: 508–522.H. HistedV. BoninRC Reid2009Direct activation of sparse, distributed populations of cortical neurons by electrical microstimulation.Neuron63508522
- 115. Yizhar O, Fenno LE, Davidson TJ, Mogri M, Deisseroth K (2011) Optogenetics in Neural Systems. Neuron 72: 9–34.O. YizharLE FennoTJ DavidsonM. MogriK. Deisseroth2011Optogenetics in Neural Systems.Neuron72934
- 116. Venkatraman S, Elkabany K, Long JD, Yao Y, Carmena JM (2009) A system for neural recording and closed-loop intracortical microstimulation in awake rodents. IEEE Trans Biomed Eng 56: 15–22.S. VenkatramanK. ElkabanyJD LongY. YaoJM Carmena2009A system for neural recording and closed-loop intracortical microstimulation in awake rodents.IEEE Trans Biomed Eng561522
- 117. Leifer AM, Fang-Yen C, Gershow M, Alkema MJ, Samuel ADT (2011) Optogenetic manipulation of neural activity in freely moving Caenorhabditis elegans. Nat Methods 8: 147–152.AM LeiferC. Fang-YenM. GershowMJ AlkemaADT Samuel2011Optogenetic manipulation of neural activity in freely moving Caenorhabditis elegans.Nat Methods8147152
- 118. Wang XJ, Buzs'aki G (1996) Gamma oscillation by synaptic inhibition in a hippocampal interneuronal network model. J Neurosci 16: 6402–6413.XJ WangG. Buzs'aki1996Gamma oscillation by synaptic inhibition in a hippocampal interneuronal network model.J Neurosci1664026413
- 119.
Efron B, Tibshirani RJ (1993) An introduction to the bootstrap. London: Chapman and Hall/CRC. 456 p.B. EfronRJ Tibshirani1993An introduction to the bootstrapLondonChapman and Hall/CRC456
- 120. Politis DN, Romano JP (1994) Limit theorems for weakly dependent Hilbert space valued random variables with applications to the stationary bootstrap. Statistica Sinica 4: 461–476.DN PolitisJP Romano1994Limit theorems for weakly dependent Hilbert space valued random variables with applications to the stationary bootstrap.Statistica Sinica4461476
- 121. Panzeri S, Senatore R, Montemurro MA, Petersen RS (2007) Correcting for the sampling bias problem in spike train information measures. J Neurophysiol 98: 1064–1072.S. PanzeriR. SenatoreMA MontemurroRS Petersen2007Correcting for the sampling bias problem in spike train information measures.J Neurophysiol9810641072