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PLOS One logoLink to PLOS One
. 2023 Feb 23;18(2):e0279987. doi: 10.1371/journal.pone.0279987

Multidimensional recurrence quantification analysis of human-metronome phasing

Caitrín Hall 1,*, Ji Chul Kim 1, Alexandra Paxton 1
Editor: Sebastian Wallot2
PMCID: PMC9949643  PMID: 36821591

Abstract

Perception-action coordination (also known as sensorimotor synchronization, SMS) is often studied by analyzing motor coordination with auditory rhythms. The current study assesses phasing—a compositional technique in which two people tap the same rhythm at varying phases by adjusting tempi—to explore how SMS is impacted by individual and situational factors. After practice trials, participants engaged in the experimental phasing task with a metronome at tempi ranging from 80–140 beats per minute (bpm). Multidimensional recurrence quantification analysis (MdRQA) was used to compare nonlinear dynamics of phasing performance. Varying coupling patterns emerged and were significantly predicted by tempo and linguistic experience. Participants who successfully phased replicated findings from an original case study, demonstrating stable tapping patterns near in-phase and antiphase, while those unsuccessful at phasing showed weaker attraction to in-phase and antiphase.

Introduction

Perception-action coordination (also called sensorimotor synchronization, SMS) occurs as people coordinate overt movements with a rhythmic stimulus [13]. This is typically studied using tasks in which participants are instructed to coordinate with auditory rhythms, which requires explicit intention to synchronize. We aim to explore coordination when participants are instructed to execute controlled desynchronization with a rhythmic stimulus. This task, called phasing, is inspired by a musical technique investigated in a case study of professional percussionists [4]. Our controlled examination of phasing provides a conceptual replication and extension of the case study.

The simplest synchronization task is coordinating rhythmic finger movements with a metronome. Within such contexts, phase dynamics are largely involuntary, while tempo change is under voluntary control [57]. People display two stable phase relationships: in-phase and anti-phase [5,8]. Individuals also display substantial tempo flexibility, coordinating from 17 bpm to 150–170 bpm for anti-phase tapping [810] and 300–400 bpm for in-phase tapping [1013]. Prior research suggests it becomes difficult to coordinate with a metronome beyond these rate limits.

Rhythmic coordination is also impacted by individual factors, such as musical and linguistic experience. Previous findings suggest musicians are better able to synchronize with auditory stimuli than nonmusicians [14,15]. Additionally, an association between increased inhibitory control and SMS abilities in bilinguals [1618] indicates multilingualism may improve rhythmic coordination. Taken together, perception-action coupling is shaped by individual differences and task demands.

Phasing

Phasing involves musicians shifting in and out of synchrony with one another while performing the same rhythm at different tempi. For example, in the musical composition “Drumming” [19], two percussionists begin by drumming synchronously. One drummer then attempts to maintain the original tempo while the other accelerates, gradually desynchronizing. Eventually, after tapping the same rhythm at different tempi, the partners approach synchrony again and return to unison by tapping at identical tempi one cycle apart.

During “Drumming,” the professional percussionists reported feeling pulled toward synchronization despite intentions to play at independent tempi [20]. To understand this, Schutz [4] conducted a case study of the percussionists performing “Drumming” (Fig 1). In theory, the accelerating and steady drummers should perform independently. In reality, however, they exhibit a push-and-pull pattern, unable to overcome the tendency toward interpersonal coupling. Inspired by Schutz’s case study, the current work investigates the evolution of coordinative behaviors during phasing with a metronome among non-expert populations using recurrence quantification analysis (or auto-recurrence quantification analysis; RQA).

Fig 1. Theoretical versus actual phasing performance.

Fig 1

Left: How phasing would occur, in theory, if partners were uninfluenced by each other’s performance. The static part (blue) remains constant, while the moving part (green) steadily shifts its metrical position. Right: Actual performance of “Drumming” by Becker and Hartenberger. The “static” part actually varies along with the moving part during phasing. In other words, the drummer who intended to maintain the original tempo was unable to do so; instead, this drummer unintentionally increased and decreased their tempo along with the phasing drummer. (Figure reproduced with permission from Schutz [4]).

Quantifying phasing with a novel application of RQA

RQA is a nonlinear time series analysis [21] that has been applied to coordination research [22,23] to quantify a single dynamical system over time [24]. Conceptually, RQA uncovers the structure of a system that changes over time through examining the patterns of repetition of a single variable of interest over time. RQA uses only one observable to describe the dynamics of multiple interdependent variables of a system, as the interacting components of a dynamical system can be uncovered from a single variable [24,25]. The idea is to reconstruct the phase space of the dynamical system, recover the trajectory of the system through that phase space, and then plot the system’s trajectory against itself to identify patterns of recurrent (or repeating) discrete states or regions of the state space. This creates a recurrence plot (RP), from which various metrics may be derived to quantify the dynamics of the system as a whole [25].

RQA has also been adapted to analyze systems with more than one measured variable and to examine the dynamics of coupled systems, including cross-recurrence quantification analysis (CRQA) and multidimensional recurrence quantification analysis (MdRQA). CRQA quantifies the coevolution of two distinct but interacting systems; in other words, CRQA captures the shared trajectories of two separate univariate systems. On the other hand, MdRQA analyzes a single system captured by two or more measured variables; that is, instead of the variables belonging to distinct time series, the variables are different dimensions of the same time series. Thus, MdRQA quantifies the auto-recurrence properties of a single multidimensional or multivariate system [25]. Readers interested in more detailed conceptual and mathematical explanations of RQA and its extensions are encouraged to consult Carello and Moreno [24] and Wallot et al. [25].

We quantify phasing by analyzing relative phase (ψ), which measures the angle between the two phasing signals in degrees. However, to date, the extensions of RQA cannot adequately handle such circular data. Because RQA-based methods operationalize similarity through the revisiting of a similar state within a given radius, RQA detects an apparent discontinuity between 359° and 0°; it calculates an angular difference of 359° even though going from 359° to 0° is a difference of only 1° in terms of ψ. Our conceptual framework necessitates that the shift from 359° to 0° be interpreted as the same ψ change as that when moving from 0° to 1°.

For the current work, we therefore created a novel circular extension of MdRQA by decomposing the relative phase signal into its x- and y-coordinates and using MdRQA to analyze them together as a multidimensional signal of the same system. Because relative phase is inherently a relational measure—in our case, a measure that necessarily accounts for the positions and relations of two phasing signals—this means that the x-- and y-coordinate values must be considered coequal and non-separable parts of a single multidimensional system. As a result, CRQA would be unsuitable for the current study, as it would treat the x- and y-coordinates as two separate but interacting systems. MdRQA, on the other hand, treats both coordinates as part of the same system, allowing us to accurately capture the system revisitations (or approximate revisitations) through specific x,y regions of the relative phase. Importantly, the choice to create and implement this novel extension of MdRQA to analyze these data came after the data were collected, as it provided for a more complete accounting of the nonlinear dynamics of the system. More information on our motives and implementation are available in the “Data Analysis” section.

In the present study, we use MdRQA to characterize multiple dimensions of a singular relative phase variable. We also use region-based MdRQA, which is the same as general MdRQA mathematically and methodologically except that it parses the RP into subsections and analyzes each subsection independently. Thus, region-based MdRQA allows us to quantify different relative phase relations separately. Like RQA, both general and region-based MdRQA yield metrics that quantify the structure, patterns, and stability of a system’s evolution. Here, we target percent recurrence (%REC), percent determinism (%DET), and maxline (MAXL). %REC is the density of recurrent states of the system across time and is proportional to the inverse of the system’s noise. %DET captures recurrent patterns of states across time, quantifying the system’s predictability. MAXL is the length of the longest run of consecutive recurrent states, corresponding to the system’s attractor strength [2527].

Present study

Inspired by Schutz [4], the present study evaluates phasing among non-expert participants with more varied musical and linguistic backgrounds. To maximize feasibility, we simplify Schutz’s task in two ways: Participants phase with a metronome instead of a partner, and the metronome produces an isochronous rhythm. Furthermore, we narrow the tempo range known to permit successful antiphase tapping to 80–140 bpm. We measure phasing by calculating ψ between participants’ taps and metronome ticks [2829]. Using MdRQA to analyze ψ, we quantify the human-metronome system’s repetitiveness (%REC), predictability (%DET), and attractor strength (MAXL). Consistent with Schutz [4] and coordination dynamics literature [5,8], we hypothesize that participants will demonstrate stable tapping near in-phase and antiphase, indicated by higher metrics during those periods.

Successfully phasing requires attending to the metronome while voluntarily adopting a different tempo than the metronome [7]. Ignoring the metronome would result in not knowing when to stop phasing, while an inability to voluntarily adopt a different tempo would cause failure to escape the in-phase attractor—a ψ near 0 throughout the task. Based on evidence of bilingual speakers’ increased selective attention [3032], we hypothesize that multilingual participants may be able to simultaneously attend to the metronome while adopting a different tempo. Monolingual participants may experience stronger coupling with the metronome. This would result in greater metrics for monolingual speakers. Furthermore, considering tapping rate limits, we expect the middle range of our selected tempi (100–120 bpm) to yield the most structured phasing performance for all participants, resulting in higher metrics. This prediction aligns with the preferred tempo range [33,34], which is the zone at which tempo perception is optimal—not so fast that individual pulses appear to fuse together and not too slow that individual pulses sound isolated.

Hypotheses

  • H1. Middle range tempi (100–120 bpm) will yield the most structured phasing for all participants. Operationalization: This will lead to higher %REC, %DET, and MAXL for trials between 100–120 bpm than trials above or below that range.

  • H2. Participants will demonstrate more stable tapping near antiphase when compared to other nonsynchronous relative phases, due to the increased general stability of antiphase relations when tapping. Operationalization: This will be reflected by higher %REC, %DET, and MAXL during antiphase.

  • H3. Monolingual participants will demonstrate stronger coupling with the metronome than multilingual speakers, due to multilinguals’ improved selective attention abilities compared with monolinguals. Operationalization: This would result in higher %REC, %DET, and MAXL for monolingual speakers overall.

As noted above, we chose to use MdRQA for the analysis after designing the study and collecting the data. This necessarily means that the operationalization of each hypothesis in terms of MdRQA metrics came later, but these operationalizations nevertheless reflected the a priori hypotheses that the study was designed to test.

Materials and methods

Participants

Twenty-five undergraduates (17 females, 8 males; 18–21 years, M = 18.7 years) at the University of Connecticut were recruited via the Psychological Sciences Participant Pool and received course credit for completing the experiment. All subjects reported normal hearing abilities and no neurological health complications. Thirteen (9 females, 4 males) reported being monolingual, and 12 (8 females, 4 males) reported being multilingual. Six (5 females, 1 male) reported experience playing one or more instruments for at least one year, while 19 (12 females, 7 males) reported no experience playing an instrument.

Sample size

As is customary in the field, results with p < 0.05 are considered significant. Experimental studies typically require 15–30 participants for adequate statistical power, which led us to recruit 25 non-expert participants for an exploratory study. We did not recruit based on a planned group comparison.

Ethics statement

The University of Connecticut Institutional Review Board approved of this study. The IRB-approved study protocol title is "Cognitive/Behavioral Investigation of Music Performance." Participants provided written consent to participate in the study.

Procedure

The procedure lasted approximately one hour. First, participants completed a demographics survey. This information was collected for IRB purposes. We did not have a priori plans to analyze anything from the survey except for musical and linguistic experience. Next, participants were introduced to the task with audio and video demonstrations (created using custom MATLAB code [35]). Tapping data were collected with a Roland HandSonic HPD-20 Digital Hand Percussion Controller [36]. After two practice sessions (see S1 Appendix for description), participants advanced to the experiment. One experimental trial consisted of the following human-metronome phasing method: The metronome’s tempo was programmed to tick at one of the seven tempi ranging from 80–140 bpm in 10-bpm increments. The metronome maintained its original tempo throughout the duration of each trial, which lasted a maximum of two minutes.

Participants were instructed to begin by tapping in synchrony with the metronome for several beats. This allowed participants to adjust to the tempo of the current trial. At the sound of a warning signal (i.e., a short, high-pitched beep), participants began phasing (see section “Phasing”) with the metronome. Here, the phasing process entailed participants increasing their tapping rate slightly while the metronome continued ticking at its original tempo. Participants were instructed to maintain their new tempo until they resynchronized with the metronome. Because the participant and metronome played at different (ideally, constant) tempi, resynchronization would happen naturally as the participant “lapped” the metronome. This can be thought of as two people running around a track at different speeds: The faster runner will gradually shift farther ahead of the slower runner until, eventually, the faster runner is one whole lap ahead of the slower runner. At that moment, both runners would be instantaneously resynchronized.

When participants resynchronized with the metronome, they were instructed to revert to the original tempo of the metronome and tap in synchrony for several beats before stopping. The period between participants’ initial desynchronization with the metronome and their resynchronization after increasing their tempo was considered one round of phasing (also referred to as one phasing lap). Participants were informed that the goal was to complete exactly one round of phasing per trial. After the drum pad detected several seconds of no tapping input, the experiment automatically continued to the next trial. Each of the seven tempi was presented three times per participant in randomized order, totaling 21 trials per participant; this allowed for a more robust sampling of the per-tempi variability than presenting it only once. The monitor displayed the total number of trials remaining.

Data inclusion criteria

Overall, our dataset included a total of 524 trials: 25 participants each completed 21 trials, three at each of the seven tempi, minus one trial that terminated early because the participant did not tap a single time. This trial was removed from our analyses.

Due to the challenging nature of the task, only 38% of trials successfully completed one round of phasing (“Successful Trials”). A further 41% completed more than one round, lapping the metronome multiple times (“Unsuccessful Trials”). The remaining 21% did not complete any rounds, resulting in zero laps around the metronome (“Incomplete Trials”). Incomplete Trials still contained tapping data and thus were able to be analyzed using MdRQA; participants simply never resynchronized with the metronome during Incomplete Trials and thus failed to execute the phasing task as instructed. Outliers were included in analyses.

All trial types were analyzed with general MdRQA, and only Successful and Unsuccessful Trials were additionally analyzed with region-based MdRQA. Analyses of Unsuccessful and Incomplete Trials are exploratory because—given the simplified task and earlier piloting—we did not anticipate such a high level of noncompliance. Music experience was excluded as a predictor because we did not achieve sufficient variability in our sample. However, music experience data is provided in participants’ data files and in S2 Appendix.

Data analysis

Open materials, data, and code

In keeping with the principles of open science, we have made our materials, data, and code for the current project fully available. Study protocols, raw tapping data (stored as MATLAB files), MdRQA analysis code (in MATLAB) [25], and descriptive and inferential statistics (in R) are available at our OSF project page: https://osf.io/4uhtb/?view_only=f8b5a974b1b54bff95abbc41a8342f5e. We used a variety of R libraries for data manipulation, visualization, and analysis, with specific implementation of each included in the open project code: ggplot2, viridis, emmeans, dplyr, tidyverse, rstatix, qwraps2, lme4, GGally, lmerTest, pander, sjPlot, and ggpubr [3750].

Relative phase (ψ) calculation

Relative phase (ψ) measures the difference between the time at which a participant taps and the nearest metronome tick, yielding the phasing relationship between participant and metronome. This was calculated as follows:

ψ=2πdtT

dt = participant’s tap time–nearest metronome tick time

T = metronome’s interbeat interval where dt is the difference between the participant’s tap time and the nearest metronome tick time and T is the metronome’s interbeat interval. The negative sign yields positive ψ when the participant taps ahead of the metronome and negative values when the participant lags behind. Thus, ψ increases when phasing is performed by tapping ahead of metronome ticks.

General MdRQA

While ψ was the only independent variable measured in the human-metronome system, these circular data were not well suited for RQA because of the apparent discontinuity in ψ when shifting from 359° to 0°; while ψ changes by only 1° during this transition, RQA calculates an angular difference of 359°, which is conceptually incorrect for our purposes. We resolved this by creating a novel circular application of RQA thanks to MdRQA.

For the circular application of MdRQA, we convert ψ into a 2-dimensional variable by wrapping ψ values to range from zero to 2Ψ; we then decompose each tap into its x- and y-coordinates by taking the cosine and sine, respectively. This converts the one-dimensional circular operationalization of relative phase into a two-dimensional representation of the same data—the x- and y-coordinates of circular relative phase as multivariate measurements of a single human-metronome system. These data are therefore more consistent with the principles of MdRQA (which captures the dynamics of a single multidimensional system) rather than those of CRQA (which captures the shared trajectories of two univariate systems).

While categorical CRQA would have been appropriate for comparing ticks of the metronome with taps of the participant (i.e., two univariate discrete time series), the decomposition of relative phase into two component parts creates two signals from the same system. However, simply conducting categorical CRQA on the metronome ticks and participant taps would not uncover the richness of the relative phase data because of the rigidity of categorical RQA techniques and the relatively short time series.

To capture the dynamics of the continuous relative phase variable, continuous MdRQA was conducted on the two-dimensional vector comprising the x- and y-coordinates of each circular relative phase value. From there, conducting MdRQA generates a recurrence plot (RP) that describes repetitions of the system’s values within a given tolerance across the phase space (Fig 2A). Here, a point on the recurrence plot indicates that a given ψ is repeated within a given radius in the time series. Recurrence metrics are then calculated from the RP. For phasing, higher %REC indicates repetition of the same ψ throughout the trial. Higher %DET means the ψ trajectory is more predictable, and higher MAXL corresponds to stronger attraction to a particular ψ.

Fig 2. Sample multidimensional recurrence plot (MdRP) produced for one phasing trial.

Fig 2

(A) How subsections were created from the MdRP to conduct region-based analysis. Each sample in the time series contains a vector of x- and y-coordinates of ψ. Recurrences or revisitations of the same multidimensional space (within a given tolerance) between the two time series (i.e., the same time series represented on the x-axis and y-axis) are plotted as points on the MdRP. (B) How participants’ taps were assigned to regions 1, 2, and 3 based on circular ψ values. As described in “Region-Based MdRQA,” synchronous taps were excluded from region-based MdRQA to effectively compare Successful and Unsuccessful Trials”.

MdRQA was performed in MATLAB [25,35]. As specified in the MATLAB files within our linked OSF page, there are five parameters that must be specified when running MdRQA: number of embedding dimensions (EMB), delay (DEL), type of norm by which the phase space is normalized (NORM), radius size (RAD), and whether the data should be z-scored (ZSCORE). We used only a single embedding dimension (EMB = 1) because we did not need to reconstruct the phase space for the current data; both dimensions of the relative phase data (i.e., the x- and y-coordinates) are represented within the dataset. As a result, we used the default delay value for unembedded data (DEL = 1). We did not normalize the phase space (NORM = ‘non’) or the data (ZSCORE = 0) because both time series exist naturally within the same scale. A small radius (RAD = 1) was chosen because the data is not highly deterministic and thus requires a radius not too close to zero to capture recurrence.

Region-based MdRQA

Using region-based MdRQA allowed us to compare %REC, %DET, and MAXL for the human-metronome system at different relative phase regions. Specifically, we were able to assess differences in recurrence, predictability, and attractor strength during nonsynchronous regions between the initial desynchronization and final resynchronization with the metronome. In other words, we focused on the system’s trajectory after it moved from synchrony, passed through antiphase, and approached synchrony again, rather than focusing on in-phase dynamics. Region-based MdRQA was conducted on both Successful and Unsuccessful Trials. We parsed taps into three non-overlapping regions based on circular ψ values: 45° ≤ ψ < 135° were region 1, 135° ≤ ψ < 225° were region 2, and 225° ≤ ψ < 315° were region 3 (Fig 2B). MdRQA metrics were calculated for each region separately using the same parameter values that were used for general MdRQA. Synchronous taps were excluded from region-based MdRQA to effectively compare Successful and Unsuccessful Trials: Although Unsuccessful Trials passed through multiple synchronous points while phasing, there were insufficient points within the synchronous region to calculate metrics.

Tempo

Because our hypotheses included predicted nonlinearities in performance across tempi, we binned tempo to create a categorical variable with three levels: lower- (80 and 90 bpm), middle- (100, 110, and 120 bpm), and upper- (130 and 140 bpm) range tempi.

Model specifications

Using the lme4 library in R [37], we created two classes of linear mixed-effects models: one to assess general MdRQA and another for region-based MdRQA. We created a separate equation for each of the three dependent variables (i.e., %REC, %DET, and MAXL) for general and region-based analyses, totaling six models. For general MdRQA, we used Incomplete Trials, monolingual language experience, and middle-range tempi as reference categories; for region-based MdRQA analyses, we used Successful Trials, monolingual language experience, middle-range tempi, and region 1 as the reference categories. We used deviation coding for all categorical variables (see S3 Appendix) [51]. For all models, participant identity was included as a random effect to control for multiple trials per participant.

Results and discussion

As described in the “Model Specifications” section (above), we analyzed data with two classes of linear mixed effects models for each MdRQA metric. Statistically significant and nonsignificant results are presented in tables; only statistically significant results (p < 0.05) are discussed in the text. For readability and clarity within the text, all statistics—including effect sizes—are presented only in the tables. We present results of our a priori hypotheses before turning to our exploratory analyses and considering future directions.

Hypothesis 1

In H1, we predicted that tempi from 100 to 120 bpm would yield the most structured tapping data. Because H1 does not consider phasing regions (e.g., synchrony, antiphase), we use general MdRQA results to assess H1. Summary statistics for general MdRQA are presented in Table 1. Results of the statistical analyses for H1 are available in Table 2.

Table 1. Descriptive statistics for general MdRQA for successful, unsuccessful, and incomplete trials.

Metric Successful (N = 200) Unsuccessful (N = 213) Incomplete (N = 111)
%REC M = 42.96, SD = 1.01 M = 42.94, SD = 0.85 M = 43.22, SD = 0.74
%DET M = 66.48, SD = 2.42 M = 66.59, SD = 2.42 M = 66.93, SD = 2.36
MAXL M = 7.64, SD = 1.81 M = 7.95, SD = 1.80 M = 8.06, SD = 1.51

Table 2. Linear mixed effect model results for general MdRQA with trial type, language experience, and tempo range as predictors of %REC, %DET, and MAXL.

Each MdRQA metric was predicted using a separate model. Marginal and conditional R2 for each model included below each model label. Effect sizes provided as standardized estimates (ß) for statistically significant predictors. As noted in the Model Specifications section, the use of deviation coding yields k-1 variables that test the difference between a given level of the categorical variable and the reference level. General MdRQA models used the incomplete trials, monolingual language experience, and middle tempi as reference categories; for more on mathematical interpretation of deviation-coded interaction terms, see Barr et al. (2013) [51].

%REC
Marginal R2 = 0.051, Conditional R2 = 0.112
Predictors Estimate SE df t-value p-value ß
(Intercept) 43.044 0.070 42.98 610.665 < 0.0001 --
Successful trials (v. Incomplete) -0.265 0.152 499.96 -1.75 0.081 --
Unsuccessful trials (v. Incomplete) -0.178 0.154 467.95 -1.157 0.248 --
Multilingual language exp. (v. Monolingual) 0.128 0.130 31.63 0.987 0.331 --
Upper tempo range (v. Middle tempo range) 0.044 0.096 488.68 0.461 0.645 --
Lower tempo range (v. Middle tempo range) -0.129 0.136 499.71 -0.944 0.346 --
Successful trials x Language exp. 0.003 0.257 494.26 0.013 0.990 --
Unsuccessful trials x Language exp. -0.137 0.265 449.04 -0.518 0.605 --
Successful trials x Upper tempo 0.040 0.232 494.29 0.174 0.862 --
Unsuccessful trials x Upper tempo 0.218 0.247 499.25 0.88 0.380 --
Successful trials x Lower tempo -0.365 0.392 501.10 -0.93 0.353 --
Unsuccessful trials x Lower tempo -0.409 0.392 502.76 -1.044 0.297 --
Language exp. x Upper tempo -0.075 0.192 488.68 -0.392 0.695 --
Language exp. x Lower tempo -0.428 0.204 491.07 -2.097 0.037 -0.109 *
Successful tr. x Lang. exp. x Upper tempo -0.069 0.463 494.29 -0.149 0.882 --
Successful tr. x Lang. exp. x Lower tempo -0.342 0.404 498.55 -0.848 0.397 --
Unsuccessful tr. x Lang. exp. x Upper tempo -0.235 0.495 499.25 -0.474 0.636 --
%DET
Marginal R2 = 0.033, Conditional R2 = 0.049
Predictors Estimate SE df t-value p-value ß
(Intercept) 66.546 0.161 58.88 412.154 < 0.0001 --
Successful trials (v. Incomplete) -0.010 0.410 457.77 -0.024 0.981 --
Unsuccessful trials (v. Incomplete) 0.081 0.412 389.10 0.198 0.843 --
Multilingual language exp. (v. Monolingual) 0.404 0.286 38.77 1.414 0.165 --
Upper tempo range (v. Middle tempo range) 0.301 0.266 492.01 1.132 0.258 --
Lower tempo range (v. Middle tempo range) -0.419 0.376 505.54 -1.115 0.266 --
Successful trials x Language exp. -0.043 0.694 438.87 -0.062 0.950 --
Unsuccessful trials x Language exp. -0.689 0.705 358.87 -0.977 0.329 --
Successful trials x Upper tempo -0.267 0.641 500.43 -0.416 0.677 --
Unsuccessful trials x Upper tempo -0.694 0.682 505.53 -1.018 0.309 --
Successful trials x Lower tempo 0.580 1.080 506.71 0.537 0.591 --
Unsuccessful trials x Lower tempo 0.807 1.078 507.00 0.748 0.455 --
Language exp. x Upper tempo -0.395 0.531 492.01 -0.744 0.457 --
Language exp. x Lower tempo -0.526 0.566 494.83 -0.93 0.353 --
Successful tr. x Lang. exp. x Upper tempo 1.549 1.281 500.43 1.209 0.227 --
Successful tr. x Lang. exp. x Lower tempo 1.818 1.114 504.98 1.632 0.103 --
Unsuccessful tr. x Lang. exp. x Upper tempo 0.609 1.364 505.53 0.446 0.655 --
MAXL
Marginal R2 = 0.073, Conditional R2 = 0.215
Predictors Estimate SE df t-value p-value ß
(Intercept) 7.942 0.168 33.58 47.34 < 0.0001 --
Successful trials (v. Incomplete) -0.196 0.283 506.36 -0.691 0.490 --
Unsuccessful trials (v. Incomplete) 0.247 0.291 504.52 0.851 0.395 --
Multilingual language exp. (v. Monolingual) 0.256 0.320 27.82 0.8 0.430 --
Upper tempo range (v. Middle tempo range) 0.612 0.176 486.74 3.477 0.001 0.16 ***
Lower tempo range (v. Middle tempo range) -0.221 0.252 493.47 -0.877 0.381 --
Successful trials x Language exp. -0.371 0.481 506.92 -0.771 0.441 --
Unsuccessful trials x Language exp. 0.306 0.501 500.55 0.61 0.542 --
Successful trials x Upper tempo 0.645 0.426 489.77 1.511 0.131 --
Unsuccessful trials x Upper tempo 0.333 0.456 492.91 0.731 0.465 --
Successful trials x Lower tempo -0.732 0.724 494.13 -1.012 0.312 --
Unsuccessful trials x Lower tempo -0.898 0.724 495.49 -1.239 0.216 --
Language exp. x Upper tempo -0.341 0.352 486.74 -0.97 0.333 --
Language exp. x Lower tempo -0.696 0.376 488.35 -1.854 0.064 -.09 .
Successful tr. x Lang. exp. x Upper tempo 0.516 0.853 489.77 0.605 0.545 --
Successful tr. x Lang. exp. x Lower tempo 0.165 0.745 492.43 0.221 0.825 --

Overall, our general MdRQA findings failed to support H1. Neither %REC (Fig 3A) nor %DET (Fig 3B) were significantly greater for middle tempi than for lower and upper tempi. MAXL (Fig 3C) did not significantly differ for middle versus lower tempi, but MAXL was significantly greater for upper tempi than for middle tempi. The attractor strength of the human-metronome system grew as tempo increased from 100–140 bpm, making it more difficult for participants to decouple from the metronome and successfully achieve phasing.

Fig 3. Effects of language experience (red: Multilingual; blue, monolingual) and tempo range on MdRQA metrics: %REC (Panel A, top), %DET (Panel B, middle), and MAXL (Panel C, bottom).

Fig 3

The metronome ranged from 80–140 bpm. In our linear mixed effects model, we binned tempo into the following categories: lower (80–90 bpm), middle (100–120 bpm), and upper (130–140 bpm). The violin plots depict the probability density of the binned tempo data at different %REC, %DET, and MAXL values. The mean value is indicated by a diamond near the center of each violin. Results of statistical analyses are located in Table 2.

Our findings might imply that our tempo selection was too narrow. Based on previous research, participants tapping at a comfortable tempo should experience a stronger pull toward attractors, resulting in more structured, repetitive tapping as reflected in greater MdRQA metrics. Our finding that participants produced the most structured data (i.e., MAXL) at upper range tempi suggested that this may have been a more comfortable tempo for phasing than lower and middle range tempi. According to previous literature, the average natural preferred tempo for people falls around 120 bpm [33,34]. To account for the difficulties of phasing (versus tapping in-phase with a metronome), we chose to center our tempo range at 110 bpm to make the task more manageable for participants. Our results, however, suggest that future phasing studies should test faster tempi.

Hypothesis 2

H2 predicted that, overall, participants would demonstrate more stable tapping during antiphase (i.e., region 2) than during other relative phases (i.e., regions 1 and 3). This would have been supported by higher %REC, %DET, and MAXL during region 2. Because H2 pertains to phasing regions, we use region-based MdRQA results to assess our prediction. Summary statistics for region-based MdRQA are presented in Table 3. Results of the statistical analyses for H2 are available in Table 4. The significant findings related to H2 include the main effect of region on %REC, %DET, and MAXL (Fig 4); interactions between trial type and region on both %DET (Fig 4B) and MAXL (Fig 4C); and interactions among language experience, tempo, and region on both %DET (Fig 5B) and MAXL (Fig 5C).

Table 3. Descriptive statistics for region-based MdRQA for successful and unsuccessful trials.

Region Metrics Successful (N = 200) Unsuccessful (N = 213)
1 %REC M = 24.84, SD = 16.20 M = 17.00, SD = 19.81
%DET M = 23.86, SD = 31.00 M = 6.63, SD = 20.17
MAXL M = 1.58, SD = 1.35 M = 0.65, SD = 0.79
2 %REC M = 25.78, SD = 14.17 M = 14.10, SD = 21.20
%DET M = 26.29, SD = 29.98 M = 10.26, SD = 26.06
MAXL M = 1.76, SD = 1.26 M = 0.54, SD = 0.82
3 %REC M = 22.06, SD = 18.45 M = 16.70, SD = 21.29
%DET M = 14.35, SD = 26.67 M = 3.92, SD = 16.10
MAXL M = 1.04, SD = 0.91 M = 0.50, SD = 0.63

Table 4. Linear mixed effect model results for region-based MdRQA with trial type, language experience, tempo range, and region as predictors of %REC, %DET, and MAXL.

Each MdRQA metric was predicted using a separate model. Marginal and conditional R2 for each model included below each model label. Effect sizes provided as standardized estimates (ß) for statistically significant predictors. As noted in the Model Specifications section, the use of deviation coding yields k-1 variables that test the difference between a given level of the categorical variable and the reference level. Region-based MdRQA models used the successful trials, monolingual language experience, middle tempi, and region 1 as reference categories; for more on mathematical interpretation of deviation-coded interaction terms, see Barr et al. (2013) [51].

%REC
Marginal R2 = 0.075, Conditional R2 = 0.084
Estimate SE df t-value p-value ß
(Intercept) 20.214 0.690 22.92 29.275 < 0.0001 --
Unsuccessful trials (v. Successful) -7.930 1.188 518.07 -6.676 < 0.0001 -.21 ***
Multilingual participants (v. Monolingual) -0.022 1.381 22.92 -0.016 0.987 --
Region 2 (v. Region 1) -2.098 1.397 1177.85 -1.502 0.133 -.08 **
Region 3 (v. Region 1) -2.000 1.397 1177.85 -1.432 0.152 --
Upper tempo range (v. Middle tempo range) -0.554 1.428 1202.04 -0.388 0.698 --
Lower tempo range (v. Middle tempo range) -2.215 1.253 1201.81 -1.769 0.077 -.05 .
Trial type x Language experience -3.365 2.376 518.07 -1.416 0.157 --
Trial type x Upper tempo range -2.530 2.874 1170.84 -0.880 0.379 --
Trial type x Lower tempo range -6.468 2.519 1180.03 -2.567 0.010 -.08 **
Language experience x Upper tempo 2.626 2.857 1202.04 0.919 0.358 --
Language experience x Lower tempo 1.225 2.505 1201.81 0.489 0.625 --
Trial type x Region 2 -3.469 2.793 1177.85 -1.242 0.215 --
Trial type x Region 3 3.915 2.793 1177.85 1.402 0.161 --
Language experience x Region 2 -4.195 2.793 1177.85 -1.502 0.133 --
Language experience x Region 3 -1.028 2.793 1177.85 -0.368 0.713 --
Upper tempo x Region 2 -4.290 3.486 1177.85 -1.231 0.219 --
Lower tempo x Region 2 -5.013 3.058 1177.85 -1.639 0.101 --
Upper tempo x Region 3 -2.267 3.486 1177.85 -0.650 0.516 --
Lower tempo x Region 3 0.115 3.058 1177.85 0.037 0.970 --
Trial type x Language exp. x Upper tempo 1.970 5.749 1170.84 0.343 0.732 --
Trial type x Language exp. x Lower tempo 1.942 5.039 1180.03 0.385 0.700 --
Trial type x Language exp. x Region 2 -5.963 5.586 1177.85 -1.068 0.286 --
Trial type x Language exp. x Region 3 1.671 5.586 1177.85 0.299 0.765 --
Trial type x Upper tempo x Region 2 0.258 6.972 1177.85 0.037 0.970 --
Trial type x Lower tempo x Region 2 10.847 6.116 1177.85 1.774 0.076 .06 .
Trial type x Upper tempo x Region 3 9.214 6.972 1177.85 1.322 0.187 --
Trial type x Lower tempo x Region 3 7.666 6.116 1177.85 1.254 0.210 --
Language exp. x Upper tempo x Region 2 8.824 6.972 1177.85 1.266 0.206 --
Language exp. x Lower tempo x Region 2 -5.888 6.116 1177.85 -0.963 0.336 --
Language exp. x Upper tempo x Region 3 8.148 6.972 1177.85 1.169 0.243 --
Language exp. x Lower tempo x Region 3 -9.221 6.116 1177.85 -1.508 0.132 --
Tr. type x Lang. exp. x Upper temp. x Reg. 2 -7.662 13.945 1177.85 -0.549 0.583 --
Tr. type x Lang. exp. x Lower temp. x Reg. 2 -4.407 12.232 1177.85 -0.360 0.719 --
Tr. type x Lang. exp. x Upper temp. x Reg. 3 -2.761 13.945 1177.85 -0.198 0.843 --
Tr. type x Lang. exp. x Lower temp. x Reg. 3 1.518 12.232 1177.85 0.124 0.901 --
%DET
Marginal R2 = 0.098, Conditional R2 = 0.170
Estimate SE df t-value p-value ß
(Intercept) 14.248 1.628 23.53 8.753 < 0.0001 --
Unsuccessful trials (v. Successful) -10.716 1.655 1117.69 -6.473 < 0.0001 -.20 ***
Multilingual participants (v. Monolingual) -0.805 3.256 23.53 -0.247 0.807 --
Region 2 (v. Region 1) 1.916 1.828 1179.76 1.048 0.295 --
Region 3 (v. Region 1) -5.143 1.828 1179.76 -2.813 0.005 -.09 **
Upper tempo range (v. Middle tempo range) 0.434 1.881 1191.33 0.231 0.818 --
Lower tempo range (v. Middle tempo range) -3.894 1.650 1192.66 -2.360 0.018 -.07 *
Trial type x Language experience -0.857 3.311 1117.69 -0.259 0.796 --
Trial type x Upper tempo range 1.534 3.821 1201.50 0.402 0.688 --
Trial type x Lower tempo range 1.412 3.344 1200.28 0.422 0.673 --
Language experience x Upper tempo 1.301 3.762 1191.33 0.346 0.730 --
Language experience x Lower tempo -1.861 3.300 1192.66 -0.564 0.573 --
Trial type x Region 2 1.117 3.656 1179.76 0.305 0.760 --
Trial type x Region 3 9.870 3.656 1179.76 2.700 0.007 .09 **
Language experience x Region 2 -7.312 3.656 1179.76 -2.000 0.046 -.06 *
Language experience x Region 3 4.158 3.656 1179.76 1.137 0.256 --
Upper tempo x Region 2 -2.983 4.563 1179.76 -0.654 0.513 --
Lower tempo x Region 2 -4.659 4.003 1179.76 -1.164 0.245 --
Upper tempo x Region 3 4.009 4.563 1179.76 0.878 0.380 --
Lower tempo x Region 3 2.559 4.003 1179.76 0.639 0.523 --
Trial type x Language exp. x Upper tempo 8.666 7.642 1201.50 1.134 0.257 --
Trial type x Language exp. x Lower tempo -0.060 6.688 1200.28 -0.009 0.993 --
Trial type x Language exp. x Region 2 -3.186 7.312 1179.76 -0.436 0.663 --
Trial type x Language exp. x Region 3 5.464 7.312 1179.76 0.747 0.455 --
Trial type x Upper tempo x Region 2 -5.961 9.127 1179.76 -0.653 0.514 --
Trial type x Lower tempo x Region 2 3.349 8.005 1179.76 0.418 0.676 --
Trial type x Upper tempo x Region 3 16.144 9.127 1179.76 1.769 0.077 .06 .
Trial type x Lower tempo x Region 3 -1.614 8.005 1179.76 -0.202 0.840 --
Language exp. x Upper tempo x Region 2 10.850 9.127 1179.76 1.189 0.235 --
Language exp. x Lower tempo x Region 2 -8.186 8.005 1179.76 -1.023 0.307 --
Language exp. x Upper tempo x Region 3 28.537 9.127 1179.76 3.127 0.002 .11 **
Language exp. x Lower tempo x Region 3 -6.732 8.005 1179.76 -0.841 0.401 --
Tr. type x Lang. exp. x Upper temp. x Reg. 2 -17.592 18.253 1179.76 -0.964 0.335 --
Tr. type x Lang. exp. x Lower temp. x Reg. 2 5.424 16.011 1179.76 0.339 0.735 --
Tr. type x Lang. exp. x Upper temp. x Reg. 3 6.188 18.253 1179.76 0.339 0.735 --
Tr. type x Lang. exp. x Lower temp. x Reg. 3 6.243 16.011 1179.76 0.390 0.697 --
MAXL
Marginal R2 = 0.192, Conditional R2 = 0.324
Estimate SE df t-value p-value ß
(Intercept) 1.013 0.084 23.30 12.022 < 0.0001 --
Unsuccessful trials (v. Successful) -0.698 0.062 1196.00 -11.284 < 0.0001 -.32 ***
Multilingual participants (v. Monolingual) -0.147 0.169 23.30 -0.869 0.394 --
Region 2 (v. Region 1) -0.028 0.067 1180.00 -0.412 0.680 --
Region 3 (v. Region 1) -0.363 0.067 1180.00 -5.393 < 0.0001 -.16 ***
Upper tempo range (v. Middle tempo range) -0.023 0.069 1186.00 -0.331 0.741 --
Lower tempo range (v. Middle tempo range) -0.247 0.061 1188.00 -4.053 < 0.0001 -.11 ***
Trial type x Language experience 0.068 0.124 1196.00 0.554 0.580 --
Trial type x Upper tempo range -0.065 0.141 1194.00 -0.461 0.645 --
Trial type x Lower tempo range -0.003 0.124 1193.00 -0.021 0.983 --
Language experience x Upper tempo 0.043 0.139 1186.00 0.313 0.754 --
Language experience x Lower tempo 0.007 0.122 1188.00 0.059 0.953 --
Trial type x Region 2 -0.280 0.135 1180.00 -2.083 0.037 -.06 *
Trial type x Region 3 0.446 0.135 1180.00 3.311 0.001 .10 ***
Language experience x Region 2 -0.323 0.135 1180.00 -2.402 0.016 -.07 *
Language experience x Region 3 0.085 0.135 1180.00 0.632 0.527 --
Upper tempo x Region 2 -0.257 0.168 1180.00 -1.531 0.126 --
Lower tempo x Region 2 -0.097 0.147 1180.00 -0.659 0.510 --
Upper tempo x Region 3 -0.221 0.168 1180.00 -1.313 0.189 --
Lower tempo x Region 3 0.233 0.147 1180.00 1.579 0.115 --
Trial type x Language exp. x Upper tempo 0.333 0.282 1194.00 1.181 0.238 --
Trial type x Language exp. x Lower tempo 0.133 0.247 1193.00 0.539 0.590 --
Trial type x Language exp. x Region 2 -0.145 0.269 1180.00 -0.539 0.590 --
Trial type x Language exp. x Region 3 -0.192 0.269 1180.00 -0.714 0.476 --
Trial type x Upper tempo x Region 2 0.033 0.336 1180.00 0.097 0.923 --
Trial type x Lower tempo x Region 2 0.345 0.295 1180.00 1.171 0.242 --
Trial type x Upper tempo x Region 3 0.557 0.336 1180.00 1.658 0.098 .05 .
Trial type x Lower tempo x Region 3 -0.143 0.295 1180.00 -0.486 0.627 --
Language exp. x Upper tempo x Region 2 0.574 0.336 1180.00 1.709 0.088 .05 .
Language exp. x Lower tempo x Region 2 -0.148 0.295 1180.00 -0.504 0.615 --
Language exp. x Upper tempo x Region 3 0.943 0.336 1180.00 2.805 0.005 .09 ***
Language exp. x Lower tempo x Region 3 -0.295 0.295 1180.00 -1.002 0.316 --
Tr. type x Lang. exp. x Upper temp. x Reg. 2 -0.238 0.672 1180.00 -0.354 0.723 --
Tr. type x Lang. exp. x Lower temp. x Reg. 2 0.115 0.590 1180.00 0.195 0.845 --
Tr. type x Lang. exp. x Upper temp. x Reg. 3 -0.438 0.672 1180.00 -0.652 0.514 --
Tr. type x Lang. exp. x Lower temp. x Reg. 3 0.635 0.590 1180.00 1.077 0.282 --

Fig 4. Effects of trial type (green: Successful; purple: Unsuccessful), tempo range, and region on MdRQA metrics: %REC (Panel A, top), %DET (Panel B, middle), and MAXL (Panel C, bottom).

Fig 4

The metronome ranged from 80–140 bpm. In our linear mixed effects model, we binned tempo into the following categories: lower (80–90 bpm), middle (100–120 bpm), and upper (130–140 bpm). The violin plots depict the probability density of the binned tempo data at different %REC, %DET, and MAXL values. The mean value is indicated by a diamond near the center of each violin. Results of statistical analyses are located in Table 4.

Fig 5. Effects of language experience (red: Multilingual; blue: Monolingual), tempo range, and region on MdRQA metrics: %REC (Panel A, top), %DET (Panel B, middle), and MAXL (Panel C, bottom).

Fig 5

The metronome ranged from 80–140 bpm. In our linear mixed effects model, we binned tempo into the following categories: lower (80–90 bpm), middle (100–120 bpm), and upper (130–140 bpm). The violin plots depict the probability density of the binned tempo data at different %REC, %DET, and MAXL values. The mean value is indicated by a diamond near the center of each violin. Results of statistical analyses are located in Table 4.

The main effect of region on %REC revealed that region 2 had significantly lower %REC than region 1, suggesting that antiphase was noisier than desynchronization and failing to support H2. Instead, region 1 had significantly greater %DET and MAXL values than region 3. In other words, the relative phase region just before returning to synchrony was the least predictable and exhibited the weakest coupling between human and metronome.

The interaction between trial type and region on %DET supported H2: Both Successful and Unsuccessful Trials yielded the highest %DET during region 2 and smallest during region 3. This meant that the human-metronome system exhibited the most predictable tapping pattern during region 2, as anticipated. Successful Trials were generally more predictable than Unsuccessful Trials.

The interaction between trial type and region on MAXL revealed findings similar to those for %DET. MAXL also peaked during region 2 for Unsuccessful Trials, which supports H2. However, MAXL peaked during region 1 for Successful Trials, opposing H2. Both trial types produced the smallest MAXL values during region 3. Together, these results suggested that those who could not successfully phase experienced the greatest attractor strength during antiphase, while those who successfully phased experienced the greatest attractor strength during their initial desynchronization from the metronome.

Interestingly, regardless of level of success with the phasing task, participants experienced the weakest coupling with the metronome when moving from antiphase to in-phase synchrony. To the contrary, human-metronome coupling was relatively stronger when shifting from synchrony to antiphase. This was demonstrated by the relative stability of taps (i.e., increased number of consecutive recurrent states) in region 1 compared to region 3, indicating differential pulls of in- and anti-phase attractors. Since in-phase synchrony is known to be a stronger attractor than antiphase, it may be more difficult to escape from synchrony toward antiphase; thus, participants passed more slowly through region 1 than through region 3. Participants resynchronized more quickly, possibly because they were moving from the weaker attractor of antiphase toward the stronger attractor of in-phase synchrony.

The significant interactions among language experience, tempo, and region on both %DET (Fig 5B) and MAXL (Fig 5C) partially supported H2. We expected participants to reach peak %DET and MAXL values during region 2 due to increased stability near antiphase. This held true across tempi for monolingual speakers, but multilinguals exhibited more variability across tempi and regions. This result suggested that tapping predictability and attractor strength varied with task parameters. The relationship between selective attention and pull toward the metronome at various relative phases is expanded upon during our discussion of H3.

Hypothesis 3

In H3, we predicted that monolingual speakers would experience stronger coupling with the metronome and therefore produce greater %REC, %DET, and MAXL than multilingual speakers would. In other words, because multilingual speakers have been shown to have greater inhibitory control compared with monolinguals, we hypothesized that multilingual participants would be better able to intentionally decouple from the metronome in order to successfully phase, as compared to monolingual participants’ anticipated difficulty overcoming the pull toward in- and antiphase tapping. We use general MdRQA to assess the effects of language experience irrespective of phasing region, and then we use region-based MdRQA to compare how monolinguals and multilinguals differed during specific regions (i.e., regions 1–3). The significant outcomes related to hypothesis 3 include an interaction effect between language experience and tempo on %REC for general MdRQA (Fig 3A), as well as interaction effects among language experience, tempo, and region on both %DET (Fig 5B) and MAXL (Fig 5C) for region-based MdRQA. Results of the statistical analyses for H3 are available in Tables 2 and 4.

As measured by %REC, tapping data became less noisy as tempo increased. Multilinguals demonstrated a sharper and greater increase than monolinguals. These findings failed to support H3, perhaps indicating that %REC during intentional decoupling is not tied to inhibitory control—a connection that had been the foundation for H3.

The significant interactions among language experience, tempo, and region on %DET and MAXL showed a pattern of results similar to those of %REC. Both %DET and MAXL increased with tempo across regions 1, 2, and 3 for multilingual speakers. Thus, the predictability (indexed by %DET) and attractor strength (indexed by MAXL) of multilinguals’ taps grew as tempo increased during all regions. Again, in contrast with H3, these findings suggested that multilingual speakers had more difficulty desynchronizing and resynchronizing with the metronome at faster tempi.

Monolingual speakers exhibited a more complex pattern: %DET and MAXL increased with tempo during region 1, remained stable across tempi during region 2, and decreased with tempo during region 3. This meant that—for monolinguals—the predictability and attractor strength of the human-metronome system were greater at faster tempi when desynchronizing and greater at slower tempi when resynchronizing. Monolingual participants had more difficulty decoupling from synchrony at faster tempi and more difficulty returning to synchrony at slower tempi.

Overall, these interactions for %DET and MAXL neither fully supported nor contradicted our predictions regarding language experience, providing a complex picture of the impacts of intentional decoupling across task complexity. Task parameters affected monolingual and multilingual participants differently. For example, multilinguals and monolinguals had opposite relationships with tempo during region 3. Suggestions for how to disentangle these findings are provided in Limitations and Future Directions.

Post hoc analyses

We did not hypothesize about how success in the phasing task would be reflected by MdRQA metrics, as we did not anticipate such a high percentage of Unsuccessful Trials. As such, we conducted exploratory analyses to identify how Successful and Unsuccessful Trials differed in their dynamics.

Post hoc analyses revealed that Successful and Unsuccessful trials exhibited significantly different dynamics and metrics (see Fig 4 and Table 4). %REC, %DET, and MAXL are all significantly greater for Successful Trials than for Unsuccessful Trials. Furthermore, Successful Trials generally supported our prediction that region 2 should yield the most structured tapping data because of the antiphase attractor. %REC, %DET, and MAXL peak during region 2 and are the lowest during region 3 for Successful Trials. Unsuccessful Trials showed a different pattern of results: Region 2 was the least noisy (as indicated by %REC) and most structured (as indicated by %DET), but attractor strength (as indicated by MAXL) waned from region 1 to region 3. The absence of a clear pattern demonstrated by Unsuccessful Trials supports the interpretation that these trials were characterized by substantially different dynamics than Successful Trials.

While many participants faced difficulty phasing, the dynamics of Successful Trials generally replicated the dynamics identified in Kim’s [52] analysis, in which expert percussionists in Schutz’s case study [4] were found to dwell near in-phase and antiphase attractors but to move between them rather quickly. One notable difference in our results is the absence of quick transitions from initial synchrony to antiphase (demonstrated by relatively high metrics for region 1); however, this difference may have resulted from the difference between phasing with an adaptive human partner versus a rigid metronome. Similarities between the Successful Trials in the current work and Schutz’s study, however, held across music experience, tempo, and task demands, suggesting that perception-action coordination dynamics during successful phasing may emerge from general principles of motor behavior and intentional decoupling.

Limitations and future directions

The present study compared Schutz’s [4] expert study to a broader population of participants using a simplified version of the original task. We replicated the phasing dynamics in non-experts during Successful Trials. Participants in Unsuccessful Trials were unable to detect ψ, meaning they failed to complete one round of phasing; these trials did not replicate patterns in Schutz’s case study. This raises the question of what shapes phasing ability. Previous literature suggests attentional flexibility [53] and neuromuscular-skeletal constraints [54] predict high-level motor skill. Although we were able to identify distinct dynamics, our study did not permit us to investigate potential reasons for differences. Future work should explore the constraints that shape the distribution of Incomplete and Unsuccessful Trials relative to Successful Trials.

While phasing dynamics of Successful Trials were similar to those observed between expert musicians [4], we do not claim that nonmusicians and non-professional musicians should be identical to expert musicians in their phasing abilities: Critical differences in the dynamics may emerge when we examine interactive phasing context. To that end, future research should utilize a dyadic phasing task with a wider tempo range and again evaluate musical and linguistic experience to investigate whether our observations extend to dyadic conditions.

Finally, future work should develop a dynamical model that captures the observed behavior and provides novel testable predictions. Such models have been influential in the study of coordination dynamics [55]. A model of phasing should account for the observed changes in attractor landscape determined by task demands and individual experience from the present work and the original case study [4] and should provide an account of dyadic phasing.

Conclusion

Inspired by Schutz’s [4] data-driven case study, we here introduced a novel phasing task that requires intentional decoupling from an auditory metronome. Our complementary approach allowed us to study perception-action coordination through traditional in-phase and antiphase tapping paradigms: Despite key differences between the two paradigms (i.e., partnered expert performance versus isochronous human-metronome phasing), we conceptually replicated the original findings [4]—that is, dwelling near in-phase and antiphase and quickly transitioning between these attractors—among participants who were able to successfully phase, regardless of individual experiences or task demands. Given these findings, similar sensorimotor coordination processes may underlie successful phasing, even for different populations performing at different rhythmic complexities (e.g., isochronous versus non-isochronous). Parallel findings from two very different populations completing similar tasks of varying difficulty provides converging evidence about the general dynamics of phasing and perception-action coordination.

Supporting information

S1 Appendix. Descriptions of practice sessions.

(DOCX)

S2 Appendix

(DOCX)

S3 Appendix

(DOCX)

Acknowledgments

The authors would like to thank Edward Large (University of Connecticut) for advice, feedback, and guidance and Matthew B. Jané (University of Connecticut) for his assistance designing the figures. This work was completed in part as coursework done by lead author C. Hall in the “Applications of Nonlinear Time Series Analyses” graduate course at the University of Connecticut, taught by coauthor A. Paxton and Steven J. Harrison.

Data Availability

All raw data, code, protocols, and other methods materials are available from the Open Science Framework database (https://osf.io/4uhtb/?view_only=f8b5a974b1b54bff95abbc41a8342f5e).

Funding Statement

This work was financially supported by the Peter and Carmen Lucia Buck (PCLB) Foundation Undergraduate Research Grant from the Connecticut Institute for Cognitive and Behavioral Sciences, which was awarded to C. Hall. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Decision Letter 0

Sebastian Wallot

24 Nov 2021

PONE-D-21-26808Multidimensional Recurrence Quantification Analysis of Human-Metronome PhasingPLOS ONE

Dear Dr. Hall,

Thank you for submitting your manuscript to PLOS ONE. I apologize for the long delay, but it took a while to find two expert reviewers that had time to closely read your manuscript. Unfortunately, the reviewers do not quite agree on the magnitude of changes that are needed for your manuscript to be accepted for publication. However, weighting all things, I decided to invite you to submit a revised version of the manuscript that addresses the points raised during the review process. You will see that both reviews agree that more information needs to be provided regarding the particular analysis, parameters settings, and presentation/interpretation of the results. However, reviewer 2 is generally more critical, and also lists a whole series of shortcomings of the paper that concern its conceptual nature, but also the general way that various aspects of literature, data, design and analysis are communicated If you consider submitting a revision of your paper, please make sure that you address all concerns raised by the two reviewers point-by-point. Particularly, it will be important that you can convice reviewer 2 that your revised version has taken majors steps towards a general improvement over the current mansucript.

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Reviewer #1: Partly

Reviewer #2: No

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2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: No

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Reviewer #1: Yes

Reviewer #2: Yes

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Reviewer #1: Yes

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5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The current study aims to test the roles of multilingualism and tempo in predicting perception-action coordination. To evaluate these effects, the authors conducted a phasing-based experiment – tapping a tempo deviated from a specific BPM played by a metronome. Innovatively, the sample did not consist of professional musicians. Due to better selective attention, the researchers hypothesized that multilingual participants would show higher rates of success in the task – defined as a return to in-phase tap after one lap of desynchronization. Further, they assessed that around both antiphase and in-phase subjects would tap more consistently, and that 100-120 BPM would be the most compatible tempi to succeed in phasing. The reasoning to hypothesize the latter was vague.

Multi-dimensional Recurrence Quantification Analysis was applied on components of the relative phase between participants' taps and original tempo set by the metronome. In this manner, the researchers evaluated several aspects of the performance on the task. Their findings did not support the hypothesis regarding the suitable tempo for phasing. Instead, they found that participants are drawn more to a specific relative phase as the tempo increases from 80 to 140 BPM. Windowed mdRQA implied that in-phase is a stronger attractor than antiphase on trials with higher tempi. While monolinguals transition in and out of synchrony is affected by tempo, multilingual subjects could keep a stable tapping rhythm across the range of BPM – corresponding with the authors' hypothesis. However, a variance test was not provided.

The paradigm was based on previous research and fitted to non-musicians, hence helping to generalize Schutz's previous findings regarding phasing. The authors declared their hypotheses precisely and returned to them in the discussion section. Also, Recurrence Quantification Analysis was an innovative and suitable way to approach this data – supported by the researchers' findings of higher mdRQA attributes on successful trials. Moreover, the supplemented data, as well as the videos, and codes were plain and explanatory.

My primary concerns are:

• The reasoning behind conducting mdRQA on the sine and cosine of the relative phase is unclear. How should a recurrence point of cosine and sine be interpreted?

• The windowed analysis’s relatively high SD for the mdRQA outcomes (REC, DET, maxL) suggests that the time series may be too short to conduct mdRQA properly. To address this point, the authors should check the average size of the recurrence plots and the histogram of the mdRQA outcomes.

• The researchers should provide the mdRQA parameters that were used for the analysis.

My minor concerns are:

• Effect size would be an essential addition to the Tukey posthoc, specifically when the degrees of freedom are high.

• In my opinion, a recurrence point should not be defined as a repetition of the same value. In this case, it seems that a recurrence point stands for similarity dependent on the chosen radius.

• Why does mdRQA fit this data better than CRQA?

If the authors address the above queries, I think the paper could contribute to the literature.

Reviewer #2: Title:

Multidimensional Recurrence Quantification Analysis of Human-Metronome Phasing

Comments to the editor and authors:

I would like to thank the authors for the opportunity to read this manuscript. The paper reports an empirical study of a ‘phasing’ task using multidimensional recurrence quantification analysis. While I appreciate the effort put in this work, the manuscript has major problems and the overall quality is far below adequate for publication. In brief, the place of this study within past research is not well established, the task is not described in enough detail, the analyses (MdRQA, regression, and posthoc tests) are not presented in enough detail, the results are not properly reported and interpreted, and some of the analyses reported are not appropriate to assess the hypotheses put forward. In addition, the text is unclear in many passages, and the limitations are not addressed.

Therefore, I have no alternative than to recommend rejecting this submission.

It would be impractical to list all problems I found in this manuscript. Below I will list some of the main issues. I hope the authors will see my comments are meant to help them improve the manuscript for a future submission.

L75ff: about RQA

The analytical framework of RQA is presented very superficially as a method “to describe nonlinearities of coupled dynamical systems”. The reader must be presented with a bit more of the conceptual (if not mathematical) background.

L76ff: about MdRQA.

Wallot et al (2016) present MdRQA as a method to “analyze group-level behavior of groups bigger than a dyad.” Given the current study design can be conceived of as involving human-metronome 'dyads', you must explain better why you chose MdRQA. Further below in the text you indicate that using MdRQA was not the initial choice but an ad hoc decision, a workaround because of issues with the data. This must be made clear.

L72: “The “static” part actually varies along with the moving part…”

This is too vague. What is it that you want the reader to attend?

L85:

Calling 25 WEIRD undergraduates with age range 18-21 “a broad population… with different musical and linguistic backgrounds” is not realistic.

L92ff Hypotheses

1) Please indicate your hypotheses and the predictions tested more clearly. I identified 3 (or perhaps 4) hypotheses/predictions:

H1: “participants will demonstrate stable tapping near in-phase and antiphase” with prediction “higher metrics during those periods.”

To test H1, I suppose one would compare inphase and antiphase, which seems related to the windowed analysis, but this is unclear. The motivation to conduct windowed MdRQA is said to be “to compare successful and unsuccessful trials” so the analytical framework and the implications for the hypothesis are confusing.

H2A: “multilingual participants may be able to simultaneously attend to the metronome while adopting a different tempo.” H2B: “Monolingual participants may experience stronger coupling with the metronome” with prediction: “greater metrics for monolingual speakers.”

To test H2, the idea seems to be to use regression analysis, but since the interactions are not properly taken into account in the report, you end up not able to compare between monolingual and multilingual participants appropriately.

Also, given you simplified the task, the prediction in L102 does not seem well justified.

H3: “we expect the middle range of our selected tempi (100-120 bpm) to yield the most structured phasing performance for all participants” with prediction “higher metrics”

To test H3, I suppose one would compare middle range with lower (80-100) and higher (120-140) ranges. But in this case, adding ‘tempo’ as a linear predictor in the models does not seem to be the appropriate way to test this. Because your prediction is that the relationship is not linear but perhaps something like parabolic: low-high-low

2) How does comparing successful and unsuccessful trials relate to the hypotheses presented? In other words, why did you add trial type as a predictor in the models?

L112: sample size

What you report is not what is commonly meant by 'determining sample size'. What exactly was the sample size determined in advance? Anything from 15 – 30? Which 'groups' did you consider relevant to determine sample size? Considering the vars gender (male/female), linguistic abilities (mono/multi), and musical experience (yes/no), you do not have 15-30 in each group.

L115 Data inclusion criteria and n of trials

Given you need to know what a trial is to understand this part, I suggest you move it to after you describe the procedure, i.e. before Data Analysis.

L115

Please justify the number of trials in the dataset. What counts as a trial, how many trials per participant, how many issues e.g. due to early termination, malfunction?

L116 , then L137

Please clarify what you mean by ‘one round of phasing’ and “complete one phasing lap”. The whole procedure is a bit unclear for the reader

L119

Given the instructions to participants, how can you not have any tapping data in some trials? What is the justification to recode these missing data as zero? If this was done merely to be able to fit the models, this is probably wrong.

L131

You mention demographics survey and then do not report/discuss anything. What exactly do you mean here?

L141ff Data analysis

1) You must report the parameters used in MdRQA and how you decided which values to use.

2) The Statistical analyses conducted must be properly described. Simply saying that you calculated descriptive and inferential statistics is too vague. You fitted regression models and you must describe what you did in detail so that readers can understand and assess your work. The structure of the models fitted must be clearly explained. For example, the tables suggests you included interactions and you did not mention that. Describe each predictor, their possible values and scale. Were they centered or standardized prior to including in the models? How did you account for repeated measures arising from multiple trials? The [ ] notation in the table suggests you used 'random' effects, if so what and why and how? One table indicates you added a 4-way interaction: trialtype*language*tempo*window but not all parameter combinations seem present. As the moment it is not at all clear that the regression models were structured (declared) properly and I have very low confidence in the reported results and their interpretation. Also, Table 5 reports post hoc tests but you did not clearly explain them.

3) As it is, the text is saying you used all these R packages to calculate statistics, which is not the case (e.g. viridis). If you indeed want to acknowledge all packages you used, you must clarify their role in the analyses.

L146

Please add at least a sentence to clarify to the reader what phi is conceptually (relative phase between participants’ taps and metronome ticks). Please format the formula correctly to improve readability.

L154:

What do you mean by 'the apparent discontinuity in Ψ near synchrony'?

L154

1)The procedure to ‘adapt’ the data for MdRQA must be better motivated and better explained (to say you “decomposed each tap into its x- and y-coordinates by taking cosine and sine” is not very clear).

2)In what ways does the procedure adapt the data to mdrqa? How did this solve the problem of 'apparent discontinuity'?

L162 windowed analysis:

1)please clarify the motivation to conduct windowed analysis: is this related to H1? How does this relate to comparing successful and unsuccessful trials?

2)Did you identify the transitions from one window to another for each time series? How?

3)Fig 2: The figure does not show MdRQA but a MdR plot. Why is the in-phase period not represented in this MdRplot?

4) Fig 2: caption is incorrect. The time series may be perhaps 'represented' in both axes, but this plot shows recurrences not the time series. The axes labels need adjusting as does the title.

L177:

Certainly not “all results”, so please clarify which results do you report (e.g. summary statistics, table of estimates from regression models). You should also consider reporting some effect sizes (e.g. relevant slopes) in the text if you want to use them to support your inferences.

L184 Fig 3

Table 2 suggests the model included interactions. But Fig 3 shows raw data and does not take interactions into account. Also, what does the error bar represent?

A general note: The tables are poorly formatted and take too much space.

L213 “significant interaction for tempo, window, and trial type”

1) Please clarify this passage, as it is not simply 'the interaction' that is relevant here but the estimated effects. Also, it is incorrect to say interaction ‘for’ A, B, and C in this context.

2) in what ways did the results “conceptually replicate” previous findings?

L214

what do you mean by ‘relative stability’?

L229: “our finding that inhibitory control varies based on language experience and tempo”

Which results specifically do you think supports your claim, please report the relevant estimates, effect sizes, and statistics.

L289 Conclusion

It is not clear that your results provided a 'broad replication of the original dynamics' reported by Schultz.

L290 “sensorimotor coordination processes may underlie successful phasing”

what would it mean to say that sensorimotor coordination processes did NOT underlie successful phasing?

A general comment about the figures

Please indicate clearly what the error bars show. The titles of figures must be revised to correct typos, grammar mistakes and to improve their meaning, especially figures 2,4, 5, and 6. For ex, it makes no sense to say ‘interaction between language experience, window, and tempo on DET’

A general comment about openly available data

Please consider making the data available in a more friendly format such as a csv or txt, as matlab is perhaps too restrictive.

**********

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Reviewer #1: No

Reviewer #2: No

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PLoS One. 2023 Feb 23;18(2):e0279987. doi: 10.1371/journal.pone.0279987.r002

Author response to Decision Letter 0


6 Jul 2022

Academic editor Sebastian Wallot advised us to upload our response to the requested changes as a separate file. See "PLOS One Response to Reviewers."

Attachment

Submitted filename: PLOS One Response to Reviewers.docx

Decision Letter 1

Sebastian Wallot

4 Aug 2022

PONE-D-21-26808R1Multidimensional recurrence quantification analysis of human-metronome phasingPLOS ONE

Dear Dr. Hall,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. Both reviewers and I agree, that the manuscript has improved substantially. While reviewer 1 is satisfied with the changes you made, reviewer 2 has raised multiple concerns regarding how the inferential statistics are done and how some of the findings are interpreted with regard to possible inferences drawn from the models you ran, and also regarding the background of the hypotheses you formulated. In a second revision, please clarify these issues or adjust your modelling procedures accordingly.

Please submit your revised manuscript by Sep 18 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Sebastian Wallot, Ph.D

Academic Editor

PLOS ONE

Journal Requirements:

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: (No Response)

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: No

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: No

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The authors improved the paper and responded thoroughly to the points of concern. In my opinion, the manuscript can now be accepted.

Reviewer #2: My recommendation is major revision.

Thank you for the opportunity to revisit this manuscript. I appreciate the effort put by the authors in rewriting the manuscript. It has improved. For example, the hypotheses and procedures are clearer now. I can say that I understand the study better now. However, the manuscript still contains many major problems, and now that I understand the procedure and analyses a bit better, new problems became evident. Most importantly, the regression models fitted are not described in enough clarity (and at least one variable may be wrongly coded), many claims are made based on wrong interpretations of 'interactions' and/or with no statistical support (some examples below).

Additionally, I now see that what the authors call a 'windowed analysis' does not correspond to what the term means by other authors using RQA because they did not use overlapping windows. What the authors did was to divide the tapping time series into periods (which they call windows 1, 2 and 3) and use these periods ('windows') as predictors in the regression models to see if RQA measures wary across periods.

I strongly suggest the authors do not use 'window' but find another term eg 'trial period' so as to distinguish from real windowed RQA.

For the common use of 'windowed' analysis, see for example:

Webber, C.L., Jr., Marwan, N. editors (2015).Recurrence Quantification Analysis: Theory and Best Practices. Springer Series: Understanding Complex Systems. Springer International Publishing, Cham, Switzerland. http://dx.doi.org/10.1007/978-3-319-07155-8).

The authors are strongly advised to discuss with a statistician how to interpret interactions in regression models.

I will point to the major issues below. I feel I have devoted more than a reasonable amount of time helping improve this manuscript, so will not try to be exhaustive.

LINE 159

H2: The prediction is at odds with the fact that data from in-phase was excluded.

My understanding is that you do not need to compare successful vs unsuccesfull trial to test the hypotheses. So, I don't follow the justification to exclude all in-phase data.

LINE 259:

"350°"

I think you mean "359°"

LINES 269, 272, and others

You say 'categorical CRQA' but in this case the correct comparison would be 'continuous CRQA.'

LINE 295:

"we were able to assess differences in recurrence, predictability, and attractor strength around in-phase, antiphase, and between those regions"

You excluded the data around in-phase (in my view, unnecessarily), so you cannot assess anything about it.

LINES 316, Model specifications.

It is still unclear how the models were fitted.

Please distinguish the variables (success, language experience, tempo range, and 'window') from the possible values (successful/unsuccesful, monolingual/multilingual, low/mid/high, 'window 1' /'window 2'/'window 3'), and indicate how the variables were coded before fitting the model. For example, something like this: trial type was coded as a binary variable with successful = 0 and unsuccessful = 1. Tempo range was coded as a categorical variable using dummy coding...

I looked at the R script and I do not understand what you mean by 'compliant' vs 'noncompliant.' Is this equivalent to successful/unsuccessful? Unclear.

I also believe there may be a serious mistake in how the tempo range data were coded. Specifically, I believe mid-range tempo should probably be coded as lowerTempi == 0 and upperTempi == 0 instead of lowerTempi == -.5 and upperTempi == -.5. Please check.

LINES 339, 348

"standard estimates"

I think you mean 'standardised' not 'standard'

Table 2

The table reports estimates for 'Successful trials' but if 'Successful trials' was the baseline what is this estimate?

The table reports estimates for 'Language experience' but if monolingual language experience was the baseline, this should be multilingual language experience, no?

The table reports estimates for an interaction between "Successful trials" and "Language experience" but if successful and monolingual were the baseline, how do I interpret this interaction effects?

Similar problems for the other interactions (e.g. Successful trials x Lower tempo)

Table 4 - similar issues to Table 2

LINE 352

"This was partially supported by the general MdRQA results for %REC"

No. The results do not partially support H1.

LINE 353

"%REC was significantly greater during middle tempi than lower tempi"

No statistical evidence provided (eg posterior predictions) for this claim. Given the interactions, you cannot simply rely on the 'fixed' (or 'main') effect of "Lower tempo range" to support this claim. Fig 3 also does not provide evidence: the red/blue lines are incorrectly used, given that tempo was binned and coded as categorical.

LINE 355

"Similarly, MAXL was significantly greater during middle tempi than lower tempi and during upper tempi than middle tempi."

No evidence provided. Given the interactions, we cannot infer this from estimates reported in Table 2 alone. And Fig 3C does not help either.

LINE 372

"Trend lines indicate predicted results"

This is not the case, given that tempo was binned into three categories and these lines show a continuous linear increase.

LINE 381

"...include the main effect of window on %REC..."

This is incorrect as it refers only to window 2, and does not consider the interactions.

LINE 384

"The main effect of window on %REC revealed that window 2 had significantly lower %REC than window 1, ..."

As above, given the interactions, this is not granted.

LINE 387

"The interaction between trial type and window on %DET..."

This is only about window 3 not 2. This omission suggests the evidence is stronger than it actually is. And this is in addition to being wrong way of interpreting interactions.

LINE 387

"both Successful and Unsuccessful Trials yielded the highest %DET during window 2 and smallest during window 3"

This is suggested by the summary stats in Table 3. But the link with the results from the regression models is unclear, hence we do not know if these differences are 'significant.'

LINE 391ff

"The interaction between trial type and window on MAXL revealed 391 findings similar to those for %DET. MAXL also peaked during window 2 for Unsuccessful Trials, which supports H2. However, MAXL peaked during window 1 for Successful Trials, opposing H2. Both trial types produced the smallest MAXL values during window 3."

Again, here the results from the regression ('interaction') is offered to support the claim that the differences reported in the summary statistics are significant. But this is not granted.

This problematic interpretation of 'interactions' is repeated multiple times, e.g. L 413, L433, (not exhaustive).

LINE 436

"As measured by %REC, tapping data became less noisy as tempo increased"

This is not supported. This interpretation may be suggested by eyeballing Fig 3, but no statistical evidence is provided, and even eyeballing Fig 3, the difference between monolingual and multilingual seems minimal. Also, to say 'as tempo increased' is not consistent with the fact that tempo was binned and treated as a categorical variable.

LINE 436

"with multilinguals demonstrating a sharper and greater increase than monolinguals."

Not supported

LINE 437

"These findings failed to support H3..."

Indeed the findings contradicted H3.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: Yes: Murillo Pagnotta

**********

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

Decision Letter 2

Sebastian Wallot

3 Nov 2022

PONE-D-21-26808R2Multidimensional recurrence quantification analysis of human-metronome phasingPLOS ONE

Dear Dr. Hall,

also reviewer 2 thinks that the manuscript has improved greatly, and hand only a few final remark where some parts of the manuscript need to be cleaned-up. If you can sumit a final revision that fixes these remaining issues, your article will be accepted for publication.

Please submit your revised manuscript by Dec 18 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Sebastian Wallot, Ph.D

Academic Editor

PLOS ONE

Journal Requirements:

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #2: (No Response)

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #2: Thank you for the opportunity to revisit this manuscript. The authors have put a lot of effort, and the analyses and their reporting are much improved and much clearer. I am happy to recommend that this manuscript be accepted for publication, and I think the few minor issues below can addressed with the editor directly.

1

the sign for relative phase (psy) is not showing due to formatting to times new roman.

2

the authors added citations to Barr et al 2013 but this work is not included in the reference list.

3

there must have been a mistake along the way when producing the current version. In the response to the reviewer, the authors say they updated line 295 to include this new text:

“In other words, we focused on the systems trajectory after it moved from synchrony, passed through antiphase, and approached synchrony again, rather than focusing on in-phase dynamics.”

But this passage does not appear in the amended manuscript.

4

About figures 3, 4, and 5. In the captions for all three figures, the authors say:

“trend lines indicate predicted results and confidence intervals of the linear mixed effects model, while individual points represent the raw data. Tempo was binned into lower, middle, and upper ranges for the analysis, while the raw data is presented at each individual tempo”

This would be perfect, but the trend lines are still incorrect in all cases. Given that the data was binned, the fitted models will produce predictions for three values of tempo: lower-range, middle-range, and upper-range. However the trend lines in the figures show predictions for 7 values corresponding to the 7 tempos in the raw data (80, 90, 100, 110, 120, 130, 140). It is not possible that the fitted models would have produced this linear increase (unless I am missing something). The authors should amend this figure to correctly represent the fitted models they report.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #2: Yes: Murillo Pagnotta

**********

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

Decision Letter 3

Sebastian Wallot

20 Dec 2022

Multidimensional recurrence quantification analysis of human-metronome phasing

PONE-D-21-26808R3

Dear Dr. Hall,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

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Kind regards,

Sebastian Wallot, Ph.D

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Acceptance letter

Sebastian Wallot

6 Jan 2023

PONE-D-21-26808R3

Multidimensional Recurrence Quantification Analysis of Human-Metronome Phasing

Dear Dr. Hall:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

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Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Prof. Sebastian Wallot

Academic Editor

PLOS ONE

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