Study 3 was motivated by the inconclusive findings of Studies 1 and 2. Additionally, our aim was to replicate the effects of agency and communion on happiness contagion we consistently observed across both previous studies. In Study 3, we used three emotional displays again and measured participants’ facial activity using electromyography (EMG). EMG captures facial activity that is barely visible or invisible to the naked eye and thus outperforms FACS-coding when measuring very subtle responses such as facial mimicry (Hess, 2021).
Initially, we were also planning to use FACS-coding, but the settings of the software we used made it impossible to record videos during the study. Specifically, iMotion 7.0 that recorded both camera input and the screen stopped the recording process the moment stimuli presentation was switched to the full-screen mode. This technical error was detected after the data collection was completed. Therefore, contrary to the preregistered protocol, FACS-coding was not performed.
Method
Participants and design
We recruited 73 university students but two participants who guessed the hypotheses were excluded from the analyses. The final sample comprised 71 participants (62 women; Mage = 25.89 years, SD = 7.27). Moreover, we could not use the EMG recordings of 7 participants because of technical problems and artifacts in the signal. Thus, the EMG analyses were based on 64 participants (55 women). Similar to Study 1, we used a 3 (senders’ emotional display: happiness, anger, sadness) × 2 (senders’ communal traits: high communion, low communion) × 2 (senders’ agentic traits: high agency, low agency) within-participants design.
Procedure and materials
The procedure of Study 3 was similar to that of Study 1 except that this time, to minimize the risk that participants would not watch twelve videos carefully, we explicitly asked them to do so. Moreover, we measured the activity of the corrugator supercilii (which lowers the eyebrows), zygomaticus major (which pulls up lip corners), and depressor anguli oris (which lowers lip corners) by the bipolar placement of surface, 8 mm diameter, Ag/Cl electrodes on the left side of the face. A ground electrode was attached to the middle of the forehead, directly below the hairline (Tassinary et al., 2007). EMG was measured using a BioPac MP150, digitized with 24-bit resolution, sampled at 1 kHz, and recorded on a PC. Raw data were filtered offline with a 20–400 Hz bandpass filter and a 50-Hz notch filter and rectified using the ANSLAB software (Blechert et al., 2016). The signal was baseline corrected (i.e., we calculated muscle activity by subtracting the baseline activity from the average of all data points in each trial). The data were standardized for each participant separately. First, they were averaged within 500 ms epochs across a trial (i.e., 35 s), which resulted in 70 data points for each trial, and the baseline including 1 s prior to the stimuli onset. Next, the data were standardized within each participant and within each muscle using mean and standard deviation computed from all collected data points across the study (12 trials × 71 data points = 852). All data points above three standard deviations were removed (1.8% of all data points). We also removed the trials containing more than 15 such data points (2.6% of all trials).Footnote 5
Participants also rated the degree to which they felt happiness (ω = .93), sadness (ω = .86), anger (ω = .88), and fear (ω = .86) using the modified DES (Izard et al., 1974) and completed two recall tasks rating the senders’ communion (rSBfist task = .93; rSBsecond task = .75) and agency (rSBfirst task = .81; rSBsecond task = .74).
Results
Manipulation check
Planned contrast indicated that participants rated the high-communion senders as more communal (M = 5.91, SD = 0.94) than the low-communion senders (M = 1.78, SD = 0.81), F(1,70) = 507.55, p < .001, ηp2 = .88 [.82, .91], and the high-agency senders as more agentic M = 6.16, SD = 0.78) than the low-agency senders (M = 2.12, SD = 0.93), F(1,70) = 499.43, p < .001, ηp2 = .88 [.82, .91]. All means and standard deviations are given in Supplementary Table S7. Taken together, these findings show that our trait manipulation was successful.
Emotional contagion
We first performed a 3 (senders’ emotional display: happiness, sadness, anger) × 2 (senders’ communal traits: high communion, low communion) × 2 (senders’ agentic traits: high agency, low agency) repeated measures ANOVA, with self-reported happiness as a dependent variable. The analysis showed a significant three-way interaction, F(2,140) = 3.08, p = .049, ηp2 = .04 [0, .11] (Fig. 5, Panel A). The first contrast was significant, F(1,70) = 128.80, p < .001, ηp2 = .65 [.51, 73]. Participants reported being more happy after seeing the happy senders (M = 4.44, SD = 1.42) than after seeing the angry and sad senders (M = 2.15, SD = 1.02). Moreover, as evidenced by the second contrast, participants reported being more happy after seeing the happy high-communion senders (M = 4.58, SD = 1.47) than the happy low-communion senders (M = 4.31, SD = 1.55), F(1,70) = 5.44, p = .025, ηp2 = .07 [.001, .21]. Finally, we observed, that the effect of communion on happiness contagion was present when the senders were high in agency (high communion: M = 4.66, SD = 1.74; low communion: M = 4.11, SD = 1.95), F(1,70) = 7.19, p = .009, ηp2 = .09 [.01, .23], while for the senders low in agency, communion did not affect happiness contagion (high communion: M = 4.50, SD = 1.68; low communion: 4.50, SD = 1.68), F(1,70) < 0.01, p = .979, ηp2 < .01 [0, .03]. Altogether, high agency fostered the effects of high communion on participants’ self-reported happiness, whereas low agency lessened these effects, thereby replicating the interactive effects of both social dimensions on happiness contagion we already observed in Studies 1 and 2.
In a similar analysis for self-reported sadness, we found no support for the predicted three-way interaction, F(2,140) = 1.30; p = .274; ηp2 = .02 [0, .07] (see Fig. 5, Panel B). Only the first contrast was significant indicating that participants reported being sadder following exposure to sadness displays (M = 3.46, SD = 1.51) than happy and angry displays (M = 1.88, SD = 0.73), F(1,70) = 82.90; p < .001; ηp2 = .54 [.38, .65]. The remaining contrasts testing the role of agency and communion on sadness contagion were not significant (Fs < 3.30, ps > 0.073). This again shows that sadness contagion occurred irrespective of the senders’ traits. As already mentioned, this result does not align with our hypotheses but corresponds to other studies showing that sadness may be shared regardless of the senders’ affiliative vs. not-affiliative characteristics (e.g., Wróbel & Królewiak, 2017; Wróbel et al., 2020). We return to this point in the General Discussion.
Next, similar to Studies 1 and 2, we analyzed participants’ responses to anger focusing on self-reported anger and fear. For self-reported anger, the analysis showed a small-sized three-way interaction (ηp2 = .05 [0, .13]) (Fig. 5, Panel C). Generally, participants reported higher levels of anger following exposure to anger displays (M = 2.64, SD = 1.42) than happiness and sadness displays (M = 1.77, SD = 0.85), as evidenced by a large effect size of this comparison (ηp2 = .28 [.11, .43]). We also found that high communion was associated with slightly less anger in response to angry senders (M = 2.54, SD = 1.58) than low communion (M = 2.73, SD = 1.47), but the effect size of this comparison was small (ηp2 = .03 [0, .13]). Finally, the effect of communion on self-reported anger was more pronounced for the senders low in agency, such that high communion was associated with less anger (M = 2.54, SD = 1.84) than low communion (M = 2.93, SD = 1.77), ηp2 = .06 [0, .18]; for the senders high in agency, the effect of communion on self-reported anger was negligible (high communion: M = M = 2.55, SD = 1.75 vs. low communion: M = 2.53, SD = 1.67), ηp2 < .01 [0, .04]. These results indicate that the two dimensions jointly modulated responses to anger. In general, more convergent responses to anger were fostered by low communion rather than high communion, which again shows that anger displays evoked reactive rather than imitative responses. Yet, across the three studies, agency modulated these responses in an inconsistent way. We elaborate on these inconsistencies in the General Discussion.
Finally, the analyses for self-reported fear showed that anger evoked complementary reactive responses (Fig. 5, Panel D). Specifically, participants reported higher levels of fear after exposure to anger displays (M = 2.76, SD = 1.33) than happiness and sadness displays (M = 1.97, SD = 0.81), as indicated by the large effect size of this comparison (ηp2 = .38 [.21, .52]). All other contrasts as well as the three-way interaction were small (ηp2 ≤ .02).
Summing up, the results of Study 3 were in line with our hypotheses and the assumptions of the Dual Perspective Model of Agency and Communion (Abele & Wojciszke, 2014) only for happiness contagion (while for sadness contagion we found no effects of the senders’ traits). The pattern we observed for self-reported anger suggested that angry expressions evoked convergent and complementary reactive responses (albeit complementary fear in response to anger occurred irrespective of the senders’ traits).
Emotional mimicry
Following the assumption that mimicry cannot be identified by the activity of single muscles (Hess et al., 2017; Olszanowski et al., 2020), mimicry to happy displays was calculated by subtracting the activity of corrugator supercilii from the activity of zygomaticus major, while mimicry for angry and sad displays was calculated by subtracting the activity of zygomaticus major from the activity of corrugator supercilli (thus, the index was analogical to that used in Study 2). Higher scores indicated more intense mimicry. We also planned to calculate an additional facial activity index for sadness by subtracting the activity of depressor from the activity of zygomaticus major, but there was cross-talk between zygomaticus major and depressor, as indicated by the positive correlation between the two (see Supplementary Table S6). Thus, we had to abandon this preregistered idea.
As we removed artifacts from the signal and thus some cases were incomplete, we used multilevel modelling (MLM) with maximum likelihood to deal with missing data and obtain unbiased estimates for means of muscle activity. MLM is based on maximum likelihood estimation that uses all of the available data to generate parameter estimates without excluding incomplete cases from the analysis (Enders, 2011). The strategy of model building was based on a priori specification of fixed effect structure that included the senders’ emotional display (happiness, anger, sadness—difference-coded with happiness as the contrast condition to which anger and sadness levels were compared), communal traits (high communion, low communion), and agentic traits (high agency, low agency). Next, we built random effect structure, starting with the simplest structure that included only intercept fit across participants, and then adding random effects of each factor (random slopes) along with their interactions. Additionally, as preliminary analysis revealed that mimicry tended to increase after the initial trials, we also tested the models with the trial number and its quadratic term (z-standardized, i.e., centered) added as a covariate. The final model was selected based on the lowest value of Akaike Information Criterion (AIC), with random effect structure that, in addition to a random intercept, included random effects of emotional display, and the covariance structure that was set as correlated (unstructured).
The results showed the expected three-way interaction, B = .938 [0.28, 1.60], t(623.6) = 2.79, p = .005 (Fig. 6). The main effect of emotional display that contrasted happiness display with two other emotional displays was also significant, B = .606 [0.29, 0.93], t(64) = 3.71, p < .001. Specifically, mimicry was more intense after exposure to the happy senders (M = 0.89; SE = 0.11) than after exposure to the sad and angry senders (M = 0.45, SE = 0.11 and M = 0.12, SE = 0.11, respectively). Next, we performed a series of simple effect analyses consistent with our hypotheses. We found that happiness mimicry was not moderated by the senders’ communion (high communion: M = 1.00, SE = 0.15 vs. low communion: M = 0.79, SE = 0.15), B = .216 [− 0.06, 0.49], t(624) = 1.56, p = .119. However, we found that for the high-agency senders, communion affected happiness mimicry, such the high-communion senders were mimicked more (M = 1.21, SE = 0.18) than the low-communion senders (M = 0.57, SE = 0.18), B = .63 [0.25, 1.01], t(624) = 13.25, p < .001; for the senders low in agency, communion did not influence happiness mimicry (high communion: M = 0.80, SE = 0.18 vs. low communion: M = 1.00, SE = 0.18), B = .199 [− 0.19, 0.58], t(625) = 1.01, p = .311.
Overall, the analysis of participants’ facial activity as measured with EMG provided additional support for the notion that agency and communion modulated participants’ responses to happiness displays in line with the Dual Perspective Model of Agency and Communion. At the same time, we observed that sadness and anger were mimicked less than happiness displays, which possibly resulted from the fact that people, in general, are more eager to imitate happiness than other emotional displays (Hess & Fischer, 2014). This may be due to the fact that although sad faces are assessed as more affiliative than angry faces, they are still less affiliative than happy faces (Hess et al., 2000).
Another important finding is that, even though agency and communion moderated happiness contagion and mimicry in a comparable way, we observed no relationship between the two processes (see Supplementary Table S6). Although no support for the mimicry-contagion link has already been reported in the literature (e.g., Hess & Blairy, 2001; Van der Schalk et al., 2011), a previous study using the same videos we used in the current study found such support (Olszanowski et al., 2020). One possible reason for this positive finding is that this study was conducted in acontextual settings (no information about the sender was provided), whereas our study, similar to other research (Hess & Blairy, 2001; Van der Schalk et al., 2011), included additional information about the senders. Possibly when no contextual information is given, the engagement of additional more controlled processes in emotional contagion is limited and thus, the relation between mimicry and contagion is easier to observe (see also Wróbel & Imbir, 2019). This suggests that, despite the fact that social factors may influence emotional mimicry and contagion similarly, different conceptualizations and operationalizations of the two processes (i.e., facial activity and self-reported emotions, respectively) may contribute to an inconsistent pattern of findings regarding the relationship between them. We should also stress that, in general, experiential, behavioral, and physiological measures of emotion are not always directly related (Fridlund, 1994; Mauss & Robinson, 2009; Parkinson, 2005), which adds to the complexity of this pattern.