1. Introduction
Spontaneous facial mimicry is a form of behavior matching [
1] that commonly occurs during face observation and facilitates emotion contagion [
2] and affective empathy [
3,
4]. Advances in robotics have enabled androids to produce human-like facial expressions [
5,
6]. Previous studies have demonstrated that humans can respond to an android’s facial expressions with spontaneous facial mimicry [
6,
7]. Classical approaches have relied on facial electromyography (EMG) to record muscle activation patterns that resemble presented facial stimuli [
8,
9,
10,
11,
12]. Alternatively, facial action patterns of participants on video recordings have been manually or automatically coded to detect mimicry using the Facial Action Coding System (FACS) [
13,
14,
15,
16,
17,
18], which analyzes facial movements in terms of anatomically based action units (AUs) [
19,
20,
21] and was designed for manual coding by human observers. Over the past decade, advances in computer vision and machine learning have enabled automated FACS coding.
In a recent study [
7], we presented participants with live performances of positive (smile) and negative (frown) dynamic facial expressions by the android Nikola (
Figure 1 and
Figure 2), which features 29 pneumatic actuators for facial actions and produces validated, human-like emotional facial expressions [
5]. Participants’ corrugator supercilii and zygomaticus major EMG activity were recorded, and their faces were simultaneously videotaped. Nikola’s frowning expressions (negative condition) elicited stronger corrugator supercilii activity in the EMG data and increased brow-lowering (AU04,
Figure 3) in the video recordings, whereas smiling expressions (positive condition) elicited stronger zygomaticus major activity and greater lip-corner puller activation (AU12,
Figure 3). Both EMG and automated FACS analysis using Py-feat [
22] previously confirmed participants’ spontaneous facial mimicry of the android’s dynamic facial expressions [
7].
However, our previous study [
7] had several limitations. First, the univariate peak-level statistics used did not account for the temporal dynamics of spontaneous facial mimicry. Second, facial mimicry involving AUs other than AU04 and AU12 was not evaluated. Third, the inference that Nikola induced participants’ spontaneous facial mimicry relied on the experimental design and prior knowledge that participants viewed Nikola’s dynamic facial expressions, whereas Nikola’s facial movements were determined solely by predefined actuator motions. Therefore, statistical evidence directly supporting a causal relationship between Nikola’s and participants’ facial expressions was lacking. Therefore, the objectives of the current study were: (1) to use multivariate time-series data and statistics to explore the nature of spontaneous facial mimicry beyond zygomaticus major/AU12 and corrugator supercilii/AU04 customarily measured in previous studies; (2) to determine the temporal latency of spontaneous facial mimicry elicited by the android Nikola; (3) to determine whether Granger causality could be assessed based on a temporal precedence effect of the mimickee (Nikola) on the mimickers (participants) during spontaneous facial mimicry; (4) to examine whether use of different statistical algorithms (participant muscular responses, time-series cross-correlations, and vector autoregression [VAR]) to evaluate the time-series data would yield converging results, e.g., whether the temporal precedence effect could be found at the lag with the maximal cross-correlation coefficient. For an overview of the theoretical and analytical frameworks of this study, please refer to
Figure 1.
Univariate statistics, such as peak-level measures or cross-correlation analysis [
17,
23,
24], are typically applied, as in the above-cited study, because EMG is usually recorded from only two or three muscles. Conversely, current automated FACS estimation from video data can simultaneously evaluate approximately 20 AUs, enabling the application of multivariate time-series statistics to detect behavioral matching [
18,
25,
26]. However, most multivariate approaches are correlational in nature and do not provide evidence for causal inference. A notable exception is multivariate Granger causality, which is grounded in the principle of temporal precedence. In the context of multivariate Granger causality, given time series X, Y, and Z (with Z potentially comprising multiple time series), if the present X is predictive of the future of
Y beyond the degree to which Y and Z already predict the future of Y, X is said to Granger cause Y [
27,
28,
29]. Moreover, Granger causality has been applied in studies of interpersonal coordination [
30,
31,
32]; however, it has not been applied specifically to facial mimicry. Several statistical frameworks are available to test Granger causality, most commonly VAR, which relies on three key assumptions: continuous-valued series, linear data-generating processes and causal effects, and discrete, regularly sampled data [
33].
In the current study, we used Py-feat [
22] to analyze video data from participants and the android. We derived trial-wise dyadic facial action time series. In each trial, the android’s face was presented to the participant for 3 s. We analyzed 105 frames per trial, corresponding to 3.5 s at 30 frames per second, to capture delayed responses in participants’ facial mimicry. Py-feat estimated AU time series are finite time series with continuous values and a regular sampling frequency, fulfilling two of the abovementioned assumptions about VAR—continuous-valued series of regularly sampled data. Multivariate VAR models can substantially increase the number of parameters to be estimated, depending on the numbers of time series and lags included.
To constrain the search for temporal effects to the most relevant AU time series, we conducted principal component analysis on Nikola’s 17 AU time series, with continuous values generated by Py-feat separately for the positive and negative conditions. We identified the two most contributory AU time series to Nikola’s smile and frown (AU25, lips part, and AU26, jaw drop, under both the positive and negative conditions;
Figure 3), as those with the highest weights in the first principal component, in addition to AU12 for the positive condition and AU04 for the negative condition, as supported by past EMG-based studies. The rationale for selecting Nikola’s most contributory AUs was related to the definition of behavioral matching and mimicry. If Nikola activated an AU during a facial expression and the participant followed suit, we could be certain that the participant engaged in spontaneous facial mimicry. If Nikola did not activate an AU, and the participant also did not, then it would be unclear whether the participant “behaved” after Nikola’s non-expression, or if the participant simply remained static. We included three AUs per agent in the mlVAR models, because six time series is the maximum that could be estimated with correlated temporal random effects in the linear mixed effect model implementation in the multilevel VAR (
mlVAR) package of R [
34].
To investigate the mimicking temporal pattern of Nikola’s most contributing AUs, we performed cross-correlation analyses between the android and participant AU04, AU12, AU25, and AU26 time series, condition-wise, to test whether the cross-correlation coefficients exceeded zero. This identified time periods during which mimicry occurred.
To investigate the temporal patterns of android–human AU temporal precedence effects, we used the
mlVAR package of R [
34]. The mlVAR models both temporal and contemporaneous effects, as well as hierarchical between-subjects effects (
Figure 1). The mlVAR model included three AUs from the dyadic data, yielding six AU time series. Although the experiment involved live performances by the android Nikola, the experimental design ensured that participants viewed Nikola’s dynamic facial expressions, whereas Nikola’s facial movements were determined solely by predefined actuator motions. Therefore, we expected to observe only the temporal effects of Nikola’s dynamic facial expressions on participants’ facial actions. We estimated all nine android–human AU temporal precedence effects across the time course to observe their dynamic evolution, and highlighted significant latencies to identify influential android–human effects. To the best of our knowledge, Granger causality has not yet been used to test spontaneous facial mimicry. We expected to observe dynamically changing temporal effects from android AUs to participant AUs. If android–human temporal effects occur across different AU pairs, it would indicate that facial responses when observing android facial expressions involve not only copying the motor pattern of individual AUs, but also the use of goal inferencing and motor planning during social cognition
This study excelled in the novel use of dyadic multivariate time-series data from both the android and participants, enabling estimation of interpretable Granger causality effects over time, and discussion in relation to the observed AU-paired cross-correlations. Both the approach and the findings are informative in terms of understanding the nature of spontaneous facial mimicry during human–android and human–human interactions [
35,
36]. There are also practical implications. The approach and findings can be applied to social androids to optimize performance in the commercial, financial, educational, and medical contexts.
4. Discussion
We examined the timing and temporal causal relationships in FACS data from simultaneous dyadic video recordings of participants viewing Nikola’s dynamic facial expressions in our previous study [
7]. Under the negative condition, cross-correlation analysis indicated that mimicry of Nikola’s frowning expression in the brow lowerer (AU04) was significant from 433.333 ms onward. This finding corresponded with the mlVAR assessment of Granger causality, which showed that Nikola’s AU04 amplitudes exerted a significant temporal effect on participants’ AU04 amplitudes throughout the entire time-course. The mimicry of Nikola’s mouth-widening expression (AU25, lips part) was also significant throughout the entire time-course. The mlVAR revealed paired android–participant AU25 Granger causality between 600 and 1000 ms. The mimicry of Nikola’s jaw-dropping expression (AU26) was significant, between 166.667 and 900 ms, corresponding to the paired android–participant AU26 Granger causality between 166.667 and 766.667 ms.
Under the positive condition, for the lip-corner puller (AU12) mimicry of Nikola’s smiling expression, the cross-correlation was significant from 466.667 ms onwards. However, the mlVAR analysis revealed significant paired android–participant AU12 Granger causality between 166.667 and 233.333 ms. For mimicry of Nikola’s mouth-widening expression (AU25), the cross-correlation was significant, between 166.667 and 700 ms, whereas the paired android–participant AU25 Granger causality was observed between 633.333 and 866.667 ms. For mimicry of Nikola’s jaw-dropping expression (AU26), the cross-correlation was significant, between 166.667 and 1266.667 ms, but no paired android–participant AU26 Granger causality attained significance.
Turning the traditionally measured AU04/corrugator supercilii and AU12/zygomaticus major, cross-correlations indicated that human–android spontaneous facial mimicry exhibited a latency of 0.4–1 s, which falls within the range reported for human–human spontaneous facial mimicry of dynamic facial expressions (approximately 0.5–0.9 s) [
14]. This finding is also consistent with the 1.18 s delay in human–android spontaneous facial mimicry reported by Hofree et al., 2014 [
6], who used a different android, Einstein. The fact that observed spontaneous facial mimicry in human–android interactions has a latency comparable to that of human–human interactions implies that participants engage in behavioral matching with the android Nikola in a manner similar to that with a human counterpart. However, for the android–participant pairs of AU25 and AU26, the mimicry appeared to occur faster (from about 200 ms onwards) than for AU04 and AU12. To the best of our knowledge, previous studies of spontaneous facial mimicry have not investigated the timing of AU25 (depressor labii and orbicularis oris) and AU26 (masseter) mimicry responses. We thus lacked previous data for comparison. This is possibly attributable to earlier findings of high saliency in the mouth compared to other facial regions [
46,
47,
48], which therefore attracted visual attention early and contributed to the rapid onset of participants’ responses in the mouth region. Future studies that incorporate simultaneous eye-tracking of participants’ visual attention are required to clarify this potential mechanism.
MlVAR revealed non-paired android–participant AU temporal precedence effects, in addition to paired android–participant AU Granger causality. Under the negative condition, android AU04 exerted temporal effects on participant AU25 between 166.667 and 766.667 ms. Under the positive condition, android AU12 exerted temporal effects on participant AU26 between 300 and 800 ms, whereas android AU25 exerted negative temporal effects on participant AU12 between 166.667 and 600 ms. This showed that the observed participant AU time series was influenced by multiple android AU actions, with temporal effects exerted at different times along the trial time course (
Figure 5B,D), likely a consequence of both non-linear and temporal integrative effects. Therefore, the time course of the temporal precedence effects appeared different from that of the pairwise AU cross-correlations. Also, the time window of significant cross-correlation coefficients did not always correspond to the time window of significant Granger causality. Furthermore, the negative temporal effect from android AU25 to participant AU12 was unexpected but could be explained by an initial visual attentional focus on the salient mouth region, which may have suppressed or delayed the zygomaticus reaction relative to the mouth reaction, despite a concurrent early positive temporal effect of the android–participant AU12 pair.
The revealed android–human temporal effects across different AUs provide additional insight into the Goal Emulation, Planning, and Mimicry (EP-M) model [
49]. According to this framework, if android–human temporal effects are observed only in identical AU pairs, spontaneous facial mimicry likely reflects a mechanical motor replica (the direct M route between the posterior temporal sulcus and inferior frontal gyrus). Conversely, if temporal effects occur across different AU pairs that are simultaneously active in the mimickee, mimicry may represent a more holistic response driven by top-down goal emulation, planning (the indirect emulation–planning [EP] route via the inferior parietal sulcus), or a mentalizing system-modulated social response [
50]. Our mlVAR results support the possibility that the EP mechanism is involved in human–android interaction. In a previous neuroimaging study, Saygin et al. [
51], demonstrated that, when observing the actions of the robotic form and the android form of android Repliee Q2, as well as the human on whom Repliee Q2 was based, using a repetition suppression paradigm, each participant’s mirror neuron system, including the inferior parietal sulcus, was more attuned with the action in the android form than the human and robotic forms. The cited authors, however, attributed the effect to the prediction error elicited by the android’s unnatural actions. However, spontaneous facial mimicry to the android does not necessarily require mentalistic attribution to androids. Given that the participants’ human likeness ratings did not correlate with the zygomaticus major/AU12 and corrugator supercilii/AU04 responses in the current dataset [
7], our results cannot be used to imply the level of mentalistic attribution that the participants have towards the android, or to establish whether spontaneous facial mimicry was modulated by the participants’ level of mentalistic attribution towards the android [
52]. However, the previously analyzed valence and arousal ratings of the current dataset showed that emotional contagion [
2,
4] was intact during human–android interactions with Nikola. It is important to investigate, in future studies, whether mentalistic attribution to androids modulates behavioral matching in human–android interactions.
It should be noted that other statistical implementations of Granger causality exist, including entropy transfer [
29,
53,
54] and neural Granger causality [
30,
55], which can estimate non-linear temporal effects. However, the standard entropy transfer method is limited to bivariate data and relies on Shannon conditional entropy [
56], which has issues such as positive bias and difficulty in assessing statistical significance [
53]. Neural Granger causality approaches such as multilayer perceptrons or recurrent neural networks show promise for multivariate time-series data [
30], provided that sufficient computational resources are available. Notably, despite the term “causality” [
27], Granger causality estimates only temporal precedence, which is just one of several criteria needed to establish causality inference [
57,
58]. Therefore, interpretations of Granger causality should be made with caution.
Several limitations of this study should be acknowledged. First, we tested only happy (smiling) and angry (frowning) facial expressions. Hence, the effects of other expressions remain to be examined. Happy and angry expressions have been most often used to explore the effects of spontaneous facial mimicry [
6,
9,
12,
59], possibly because it is practical to detect (via surface EMG measurement) movements of the zygomaticus major and corrugator supercilii. The current study was originally designed to measure EMG, although we also collected dyadic facial video recordings, as also analyzed in the current study. However, the android Nikola shows valid facial expressions of all six basic emotions [
5], as well as complex emotional states such as awe and “flirty face” [
60]. The suggestion that Nikola is suitable for investigating a variety of emotions is a promising direction for future research. Second, the test setting was a laboratory, specifically a soundproof room, with both the android and the participant facing a prompter, and the android always against a sterile background. Although this setting ensured consistency across other visuo-audio conditions throughout the experiment, participants’ experiences of interacting with the android may have differed from those in more naturalistic social settings, such as in a commercial, financial, or medical context. Third, although the sample size of the current study was sufficient for drawing group inferences (see
Section 2.1), it was too low to allow us to investigate the effects of individual differences [
61]. Furthermore, for AU12 under the positive condition, previous analysis of zygomaticus major and AU12 responses via between-condition comparisons yielded significant results [
7]. However, the peak cross-correlation coefficients were not normally distributed, and the between-condition comparison of the peak cross-correlation coefficients was significant only on the standard
t-test, not when the robust Yuen’s trimmed mean test was applied. The non-normal distribution of the correlation coefficients, together with a larger standard error (
Table 2), imply that individual variation was greater for AU12/zygomaticus mimicry than for other AU mimicries. Although paired
t-tests with more than 25 observations are considered robust to violations of the normality assumption [
42], a larger sample size should further help avoid such issues. It is important that future studies investigate how variables such as participants’ sex [
62], age, socioeconomic status [
63], trait empathy, autistic traits [
64,
65,
66], social anxiety [
67], and attitudes towards robots and technology [
68,
69] modulate spontaneous facial mimicry to robotic facial expressions.