Abstract
In the present study, we examined the effects of explicit knowledge, obtained through instruction or spontaneous detection, on the transfer of visuomotor sequence learning. In the learning session, participants learned a visuomotor sequence, via trial and error. In the transfer session, the order of the sequence was reversed from that of the learning session. Before the commencement of the transfer session, some participants received explicit instruction regarding the reversal rule (i.e., Instruction group), while the others did not receive any information and were sorted into either an Aware or Unaware group, as assessed by interview conducted after the transfer session. Participants in the Instruction and Aware groups performed with fewer errors than the Unaware group in the transfer session. The participants in the Instruction group showed slower speed than the Aware and Unaware groups in the transfer session, and the sluggishness likely persisted even in late learning. These results suggest that explicit knowledge reduces errors in visuomotor skill transfer, but may interfere with performance speed, particularly when explicit knowledge is provided, as opposed to being spontaneously discovered.
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Introduction
Learning of sequential movements, such as typing on a keyboard or driving, consists of explicit and implicit processes. Explicit knowledge may also concern a sequence itself or a transfer rule between sequences. For improvement of sequential movements, explicit knowledge plays an important role (e.g., Benson et al. 2011). Explicit knowledge can be obtained in two ways: knowledge can be detected spontaneously, or provided by others. In the former, individuals spontaneously notice reportable rules during learning a new sequence or transferring the learned sequence. In the latter, an individual is instructed regarding the sequence itself or the rule by another person prior to learning or transfer.
Regardless of the method used to obtain explicit knowledge, a likely consensus is that explicit knowledge contributes to improvements in early phases of learning a sequence, while in some paradigms, such as rotary pursuit or mirror tracing, explicit knowledge of the transfer rules do not appear to contribute (Gabrieli et al. 1993; Heindel et al. 1989). For example, explicit knowledge by spontaneous detection can lead to faster sensorimotor adaptation (Werner and Bock 2007) and faster performance of sequential learning (e.g., Willingham et al. 2002). Similarly, explicit knowledge by instruction or strategy can lead to faster adaptation to walking on a split-belt treadmill (Malone and Bastian 2010), fewer errors with sensorimotor adaptation (Benson et al. 2011), and faster performance of sequential learning (Stefaniak et al. 2008). However, only a few studies have examined the effects of the manner in which learners obtain explicit knowledge on sequential performances (e.g., Curran and Keele 1993), while findings regarding the effects of spontaneous discovery and explicit instruction on learning have been a source of controversy in the field of education and learning science (e.g., Klahr and Nigam 2004; Dean and Kuhn 2006).
In a study of sequential learning, Curran and Keele (1993) asked participants to perform a serial reaction time task (Nissen and Bullemer 1987). In this task, participants observe visual stimuli successively presented at one of four or six horizontally aligned locations and respond with spatially compatible keys, as quickly and accurately as possible. A predetermined sequence, composed of 6–12 key presses, was repeated in the majority of trial blocks, while in a few trial blocks a randomly generated sequence was presented. Participants were assigned to one of the following three groups: intentional, more aware, and less aware groups. In the intentional group, the participants were instructed regarding the repeated sequence prior to starting the task. The participants who became aware of the repeated sequence without the explicit instruction were assigned to the more aware group, and those who were not aware of the repeated sequence were assigned to the less aware group. Curran and Keele (1993) found that the difference between reaction times to the repeated and random sequences (i.e., learning effect) was the largest in the intentional group, followed by the more aware group, with the smallest difference being observed in the less aware group. Next, a secondary task was introduced, following these single-task trial blocks, in which participants listened to a high- or low-pitch tone presented between each of the visual stimuli and were required to report the number of high-pitch tones at the end of each block. Interestingly, the learning effects did not differ among the three groups; the already acquired sequential representations in the single-task trial blocks could not be presented in the dual-task trial blocks. In the dual-system model on sequence learning (Keele et al. 2003; see also; Abrahamse et al. 2010), a set of unidimensional modules detect and utilize all available regularity within sequence information, and a multidimensional module allows sequence learning across types of information. According to this model, the system isolated by dual-task conditions corresponds to a unidimensional system and learning within this system is implicit. Additional learning under single-task conditions corresponds to a multidimensional system, with explicit learning depending on this system (see also Grafton et al. 1995; Hazeltine et al. 1997). The latter system also can learn associations within the single dimension of single-task learning, regardless of the capacity of multidimensional system, unless interference from a secondary task occurs. Thus, the explicit knowledge of the sequence obtained by instruction itself had a more favorable effect on the serial reaction time task than that observed with spontaneous discovery, which indicates that the instruction of the sequence rule contributes to development of the multidimensional system earlier. However, the benefit vanished when a secondary task, requiring cognitive or attentional resources, was introduced.
Even much less is known about the effect of explicit instruction on transfer of transformation (e.g., Watanabe et al. 2006; Tanaka and Watanabe 2014a, b). For example, if spatial button configurations of a learning sequence were horizontally mirrored in a transfer session (e.g., Tanaka and Watanabe 2014b), and participants received an explicit instruction of the transformation rule (not the transformed sequence), participants would be required to transform the learning sequence. Given that this transformation requires additional cognitive processes, benefits of explicit transfer could be abolished, according to the dual-system model (Keele et al. 2003).
In the present study, we were interested in whether benefits of explicit knowledge on transfer of a visuomotor sequence could be observed, and whether the manner in which learners explicitly obtained a transfer rule would modulate their performance during transfer. For this, we employed a sequential button press task, called the m × n task (e.g., Hikosaka et al. 1995, 1996, 2002; Tanaka and Watanabe 2013, 2014a, b, 2016). The experimental device consisted of 16 light-emitting diode (LED) buttons mounted in a 4 × 4 matrix. Experimental trials consisted of a triad (m), comprising three sequential button presses ([1] [2] [3]), and a sequence, comprising seven consecutive triads (n; i.e., 3 × 7 task). In this task, participants were required to learn the sequence, via trial and error. Following completion of the learning sequence, they were asked to perform another sequence in which the order of each triad was reversed ([3] [2] [1]; Tanaka and Watanabe 2014a). Before the transfer session, we classified participants into either the Non-instruction or the Instruction group. For the Non-instruction group, we did not provide the participants with any information regarding the reversal rule prior to the transfer session; therefore, some participants spontaneously noticed the reversal rule during the transfer session and some did not (i.e., Aware and Unaware groups). For the Instruction group, we informed the participants about the reversal rule prior to the transfer session with the second sequence. The Aware and Instruction groups were similar in their discovery of explicit knowledge; however, the underlying differences between the groups may be present. Hence, we mainly focused on differences of performance between the Aware and Instruction groups. As both the Aware and Instruction groups were presumed to obtain the same explicit knowledge of the rule, we were interested in whether speed, not the number of error trials (i.e., accuracy), differed in the Aware and Instruction groups. Note that, in our study, the explicit knowledge concerned a transfer rule (e.g., the reversal rule between the sequences) rather than the sequence itself (e.g., Curran and Keele 1993). Here, we regarded that the acquisition of explicit knowledge of a transfer rule likely corresponds to the secondary task in Curran and Keele (1993), because in the transfer session the participants mainly tried to decipher a given sequence with transformation of the acquired sequence. Similar to the results of Curran and Keele (1993), one prediction was that the explicit instruction of a transfer rule would be beneficial, even in the transfer session, if it spares cognitive load. However, other possibilities could not be ignored. Specifically, instruction might not have a greater effect than that of spontaneous detection of the rule, or the explicit instruction could even have a detrimental effect on transfer, if it requires a larger cognitive load to transfer the acquired sequence.
Methods
Participants
Sixty-three individuals (38 men, 25 women; 18–28 years old; 57 right-handed, according to self-reports) participated in the study. All participants had normal or corrected-to-normal visual acuity, normal motor function, and were naïve to the purpose of this study. The experiment was approved by the institutional review board of The University of Tokyo and was conducted in accordance with the ethical standards in the 1964 Declaration of Helsinki. All participants provided informed consent prior to commencement of the experiment.
m × n task
Stimuli and procedure
We adopted a similar experimental paradigm as those used in previous studies (e.g., Hikosaka et al. 1995, 1996, 1999, 2002; Sakai et al. 1998, 2003, 2004; Tanaka and Watanabe 2013, 2014a, b, 2016; Watanabe et al. 2006, 2010). The experimental device consisted of 16 LED buttons, mounted in a 4 × 4 matrix, and another LED button (called the “home key”) positioned at the bottom of the device (Fig. 1a). The LED buttons were square in shape (10 × 10 mm) and positioned 8 mm apart.
When the home button was pressed for 500 ms, three buttons (i.e., a triad) were illuminated simultaneously. Seven triads were presented in a fixed order, which we simply called a “sequence.” Participants were asked to press the three illuminated buttons in a predetermined order with the index finger of their dominant hands. That is, they were required to uncover the correct sequence order, via trial and error. If button presses were successful, the LEDs deactivated, one by one, and the subsequent triad was activated. Participants were then required to discover the correct order of the triad again. When button presses were incorrect, all LEDs were briefly illuminated, and the trial was regarded as an error trial. Then, participants were required to restart the sequence from the beginning, using the home button (i.e., repetition of the first triad). A trial was only regarded as successful when participants completed a sequence (i.e., seven triads) without error. The same sequence was repeated until participants completed it successfully for 20 cumulative trials. Participants were asked to perform the sequence as quickly and accurately as possible after they started a trial (i.e., pressed the home button).
We prepared two types of sequence: “Original” and “Reversed.” The Original sequence was generated randomly for each participant. In the Reversed sequence, the order of button presses was reversed from that used in the Original sequence (i.e., the spatial configurations of the triads were not changed). Tanaka and Watanabe (2014a) adopted the Reversed sequence in the transfer session and found that 50% of participants noticed the reversed rule; therefore, we expected that this sequence would likely lead to a balanced proportion regarding awareness of the transfer rule.
All participants performed a learning session using the Original sequence and, after a 5-min break, a transfer session using the Reversed sequence. Before commencement of the transfer session, participants were assigned into either the Non-instruction (n = 41) or the Instruction group (n = 22). Importantly, the Non-instruction group was not provided with any information regarding the reversal rule and was instructed that a new sequence would be randomly generated. By contrast, the Instruction group received the reversal rule in the transfer session.
Interview
Following completion of the transfer session, the Non-instruction group was asked whether they had noticed anything peculiar during the transfer session. If participants reported the reversal rule, they were assigned to the Aware group. In order to determine whether the remaining participants did not report the rule despite noticing it, an experimenter explained the rule and asked them whether they had become aware of the rule while performing the transfer session. Those who reported that they had become aware of the rule were also assigned to the Aware group, and the remaining participants were assigned to the Unaware group. This procedure was identical to that in Tanaka and Watanabe (2014a, b).
Various methods to distinguish explicit and implicit knowledge have been used. Ashby et al. (1998) suggested that implicit learning could be assumed as the result when participants could not verbalize what they had learned. Ziori and Dienes (2006, 2008) adopted subjective measures, based on confidence ratings. Importantly, the present experiment itself is an explicit learning paradigm, and we only focused on whether or not participants noticed the rule during the transfer session and could report it. Therefore, we defined explicit knowledge as participants being able to verbalize the transfer rule.
Visuospatial working memory task
In order to observe individual differences in cognitive performance between the Unaware, Aware, and Instruction groups, we adopted a computerized visuospatial working memory (VSWM) task used in a previous study (Bo et al. 2011, which was modified from Luck and Vogel 1997). Bo and Seidler (2009) showed that VSWM capacity could predict the rate of explicit motor sequence learning. Thus, if the Aware group had cognitive superiority to the Unaware group, the difference could be represented by VSWM capacity.
All stimulus arrays were presented within a 9.8° × 7.3° region on a CRT monitor with a gray background (9.3 cdm−2). Nine discriminable colored squares (0.65° × 0.65°) were prepared (red, orange, yellow, green, blue, violet, pink, white, and black). Each trial began with a central fixation cross (1.0° × 1.0°), followed by a sample array for 100 ms, a 900-ms blank screen delay, and a 2000-ms presentation of a test array. The arrays consisted of 2–8 (array size) colored squares which were randomly selected from the nine colors. For each trial, the test array was either the same as the sample array (50% of the trials) or different from the sample array (50% of the trials). Note that, in the different array, only one color of the squares was changed from the sample array, and the same color squares did not appear in each trial. Thus, participants needed to detect a change in color at different locations. Participants were then prompted to indicate whether the test array was the same as or different from the sample array by key press (same, left key; different, right key; Fig. 1b). Participants performed 252 trials in sum: 7 types of array size × 2 types of array (same or different) × 18 iterations. Participants had a seat approximately 60 cm away from the monitor. Before the commencement of the experiment, the experimenter showed participants all colored squares simultaneously and confirmed that all participants could discriminate them clearly.
Data analysis
We counted the number of error trials committed prior to completing one correct trial (i.e., accuracy). For example, the number of errors in the first successful trial (e.g., Fig. 2a) indicates the total number of errors committed by the first successful trial. We also measured the time that elapsed from the moment the home key was pressed to the moment the third button of the final (7th) triad was pressed, in each successful trial (i.e., speed). Particularly, the performance time in successful trials was fit with the power function for each participant (c.f., the power law of practice, Speelman and Kirsner 2005): y = αx β. α represents the overall (and initial) speed, with a smaller value indicating faster initial performance time. β represents the learning efficiency, with larger negative values indicating higher learning efficiency. This fitting was used in a previous work utilizing the m × n task (Watanabe et al. 2010).
As for the number of errors, we conducted two-way mixed ANOVAs with the 20 successful trial sections as a within-subject factor and the three experimental groups as a between-subject factor. As for the overall speed and learning efficiency, we conducted a one-way ANOVA, with the three experimental groups as a between-subject factor, respectively. Post hoc tests were performed using Shaffer’s method where appropriate. Effect sizes (η p 2) are reported for all ANOVAs. Difference-adjusted pooled confidence intervals for independent means were also adopted, and 95% confidence intervals are reported for the main results (Baguley 2012). VSWM capacity was calculated using the formula: K = Size of the array × (observed hit rate − false alarm rate) (Vogel and Machizawa 2004). Then, the mean K across all array sizes was computed to represent the working memory capacity for each participant.
Results
Of the 63 participants, five were excluded from the following data analysis: three were because the overall speed in the learning session was greater than two standard deviations from the mean overall speed, and two were because the overall speed in the transfer session was greater than two standard deviations from the mean overall speed of the group (one was assigned to the Unaware group and the other was assigned to the Aware group).
Learning session in the m × n task
A one-way ANOVA on the number of error trials in the learning session revealed a significant main effect of successful trial section [F(19, 1083) = 220.09, p < 0.0001, η p 2 = 0.79; Fig. 2a]. Post hoc tests indicated that the mean number of errors was larger by the first successful trial (27.01 trials) relative to the other sections (less than 1.68 trials, ps < 0.01). As for speed, the results of power fitting model (y = αx β) showed that overall speed (α) was 15.54 (p < 0.0001) and learning efficiency (β) was −0.09 (p < 0.0001; Fig. 2b). The rapid improvement of accuracy (i.e., the number of errors) and relatively slow improvement of speed (i.e., learning efficiency) reflected parallel learning of the sequence, meaning that individuals first acquire effector-independent representations and then effector-dependent representations (e.g., Hikosaka et al. 1995; Sakai et al. 1998, 2003; Tanaka and Watanabe 2013, 2014a, b).
Relationship between sequence learning and visuospatial working memory
We examined the relationship between performances of sequence learning and VSWM capacity (i.e., K). First, the results of Pearson’s correlation analysis for the total number of error trials in the learning session and K revealed a significant correlation [t(56) = 3.03, r = −0.37, p < 0.01; Fig. 2c], which indicates that participants with a larger VSWM capacity can perform a sequence with fewer errors. By contrast, the results of Pearson’s correlation analysis for overall speed and K, and learning efficiency and K did not showed significant correlations [overall speed and K, t(56) = 0.22, r = −0.029, p = 0.82; learning efficiency and K, t(56) = 1.27, r = −0.16, p = 0.20; Fig. 2d, e]. These results may suggest that participants with a larger VSWM capacity can acquire a given sequence earlier (e.g., Bo and Seidler 2009). Therefore, the present results, so far, could be assumed to replicate and verify the previous results in both visuomotor sequence learning and VSWM tasks.
Comparison of the Unaware, Aware, and Instruction groups
Through the interview for the Non-instruction group, we found that 19 participants spontaneously discovered the reversal rule during the transfer session (i.e., Aware group) and 17 participants did not (i.e., Unaware group). Therefore, the Unaware, Aware, and Instruction groups included 17, 19, and 22 participants, respectively.
Working memory capacity
Mean VSWM capacity of the Unaware, Aware, and Instruction groups was 2.60 [95% CI (2.37 2.84)], 3.05 [95% CI (2.78 3.32)], and 2.90 [95% CI (2.66 3.14)], respectively. A one-way ANOVA showed a significant main effect of group [F(2, 55) = 3.38, p < 0.05, η p 2 = 0.10; Fig. 3a]. Post hoc tests showed that the VSWM capacity was larger in the Aware group than that in the Unaware group (p < 0.05), but it was not significantly different between the Aware and Instruction groups (p = 0.38), and the Unaware and Instruction groups (p = 0.079). Interestingly, this result suggests that participants with a larger VSWM capacity tended to notice the hidden relationship between learning (first) and transfer (second) sequences. Those with a larger VSWM capacity, who can perform a sequence in a shorter time, typically may display this larger capacity in the multidimensional system (Bo et al. 2011; Keele et al. 2003). Given this assumption, the multidimensional system in those with larger VSWM capacities was not fully occupied by the transfer task (i.e., trial-and-error processes), and accepted an entry about the relationship between the learning and transfer sequences (i.e., transformation rule), resulting in the awareness of the rule.
Note that, in the present study, we classified the participants in the Non-instruction group into the Aware and Unaware groups through interview and found the significant difference of K. By contrast, the participants in the Instruction group were randomly recruited and were not sorted by any criteria; therefore, the VSWM capacity in the Instruction group must be similar to the mixture of those in the Aware and Unaware groups. In other words, even though we did not find significant differences between the Aware and Instruction, and Unaware and Instruction groups, it is reasonable to assume that original cognitive ability, such as VSWM capacity, might be generally different among the three groups.
Learning session
Mean total number of error trials in the Unaware, Aware, and Instruction groups was 38.64 trials [95% CI (27.49 49.79)], 27.26 trials [95% CI (21.96 32.55)], and 31.40 trials [95% CI (23.95 38.86)], respectively. Two-way ANOVAs on the number of error trials (3 experimental groups × 20 successful trials) did not show a significant main effect of experimental group [F(2, 55) = 2.08, p = 0.13, Fig. 3c]. However, the interaction between experimental group and successful trial section was significant [F(38, 1045) = 27.93, p < 0.0001, η p 2 = 0.10]. Post hoc tests revealed that the number of error trials by the first successful trial was larger in the Unaware group than that in the Aware group [t(55) = 2.61, p < 0.05], while it was not significantly different between the Unaware and Instruction, and Aware and Instruction groups [ts(55) < 1.50, ps > 0.13]. This difference likely reflects the discrepancy of VSWM capacity (i.e., participants with a larger VSWM capacity could perform a given sequence with fewer errors, Fig. 3b).
Mean performance time in successful trials in the Unaware, Aware, and Instruction groups was 12.47 s [95% CI (11.57 13.38)], 12.28 s [95% CI (11.46 13.11)], and 13.19 s [95% CI (12.57 13.81)], respectively. Overall speed (α) in the Unaware, Aware, and Instruction groups was 15.48 [95% CI (14.18 16.78)], 15.65 [95% CI (14.03 17.27)], and 15.67 [95% CI (14.51 16.83)], respectively. Learning efficiency (β) in the Unaware, Aware, and Instruction groups was −0.10 [95% CI (−0.12 −0.076)], −0.11 [95% CI (−0.14 −0.075)], and −0.078 [95% CI (−0.10 −0.051)], respectively. Both two-way ANOVAs on speed index (i.e., overall speed and learning efficiency) did not reveal a significant main effect of experimental groups [Fs(2, 55) < 1.44, ps > 0.24, Fig. 3c], which indicates non-significant differences of original speed among the Unaware, Aware, and Instruction groups.
Transfer session
Mean total number of error trials in the Unaware, Aware, and Instruction groups was 28.00 trials [95% CI (18.60 37.40)], 7.52 trials [95% CI (4.07 10.97)], and 2.90 trials [95% CI (1.26 4.550], respectively. Two-way ANOVAs on the number of error trials showed a significant main effect of experimental group [F(2, 55) = 27.45, p < 0.0001, η p 2 = 0.49, Fig. 4a] and successful trial section [F(19, 1045) = 56.67, p < 0.0001, η p 2 = 0.50]. The interaction between experimental group and trial section was also significant [F(38, 1045) = 25.38, p < 0.0001, η p 2 = 0.48]. Post hoc tests regarding experimental groups showed that the number of errors was larger in the Unaware group than those in both the Aware and Instruction groups [ts(55) > 5.61, ps < 0.001], while it was not significantly different between the Aware and Instruction groups [t(55) = 1.35, p = 0.18]. This difference could be mostly explained by the number of errors until the first successful trial (p < 0.001) and was simply due to a benefit of explicit knowledge of the sequence in the Aware and Instruction groups.
Since we found a significant correlation between VSWM capacity and the number of errors in learning session, we also performed Spearman’s rank correlation analysis for the total number of error trials in the transfer session and K in each group (Fig. 4b). The results showed a significant correlation in the Unaware group (S = 1425.2, ρ = −0.74, p < 0.001), not in the Aware and Instruction groups (Aware, S = 1317, ρ = −0.15, p = 0.52; Instruction, S = 1339.5, ρ = 0.24, p = 0.27). This result indicates that the correlation between the number of errors and K was retained, even in the transfer session, unless participants obtained the explicit knowledge of the rule. That is, if participants believed that they performed the task with a randomly generated sequence in the transfer session, their accuracy was related to K. If they noticed or received the explicit knowledge of rule, their accuracy was not related to the VSWM capacity.
Mean performance time in the Unaware, Aware, and Instruction groups was 11.85 s [95% CI (11.01 12.69)], 12.50 s [95% CI (11.55 13.46)], and 14.19 s [95% CI (13.29 15.08)], respectively. Overall speed (α) in the Unaware, Aware, and Instruction groups was 15.11 [95% CI (13.33 16.90)], 17.04 [95% CI (15.29 18.79)], and 20.00 [95% CI (17.81 22.19)], respectively. Learning efficiency (β) in the Unaware, Aware, and Instruction group was −0.11 [95% CI (−0.15 −0.067)], −0.14 [95% CI (−0.17 −0.11)], and −0.15 [95% CI (−0.19 −0.12)], respectively. A one-way ANOVA on overall speed revealed a significant main effect of experimental group [F(2, 55) = 6.93, p < 0.01, η p 2 = 0.20; Fig. 4d], and post hoc tests showed that the overall speed was slower in the Instruction group than that in both the Aware and Unaware groups [ts(55) > 2.28, ps < 0.05], but was not significantly different between the Aware and Unaware groups [t(55) = 1.39, p = 0.17]. By contrast, a one-way ANOVA on learning efficiency did not reveal a significant main effect of experimental group [F(2, 55) = 1.75, p = 0.18; Fig. 4e]. The slower overall speed in the Instruction group than that in the Aware group, and non-significantly different learning efficiency between the Instruction and Aware groups, indicates that the slower speed in the Instruction group persisted even in late learning.
In addition, in order to consider individual differences, because original cognitive performance of the Aware and Instruction groups should be different, we calculated improvements in speed in the transfer session in the Aware and Instruction groups and compared them. In each participant, mean performance time in the transfer session was subtracted from that in the learning session, and the value was divided by the mean performance time in the learning session: (P learn − P transfer)/P learn. A Welch unpaired t test showed a significant difference [t(37.22) = 2.08, p < 0.05, Fig. 4f], which indicates that the improvement in speed was also larger in the Aware group [mean −1.84%, 95% CI (−5.28 1.58)] than that in the Instruction group [mean −7.57%, 95% CI (−12.17 −2.97)]. Interestingly, improvements in speed in the Instruction group were less than zero, indicating the occurrence of interferences between the learning and transfer sessions [one-sample t test for the improvements in the Instruction group and zero t(21) = −3.42, p < 0.01], while those in the Aware group were not [t(18) = −1.13, p = 0.27].
Correlations between speed and accuracy in the transfer session
Although we did not find a significant difference of the number of errors in the transfer session between the Aware and Instruction groups, participants in the Aware group believed that at the beginning of the transfer session the sequence in the transfer session was newly generated and they tried to decipher the correct orders of the sequence. In order to confirm that the slower overall speed in the Instruction group than that in the Aware group was not related to the number of errors in the transfer session, we performed Spearman’s rank correlation analyses on the overall speed and the total number of errors, and learning efficiency and the total number of errors in the Aware and Instruction groups separately, as well as in combined data of these two groups. The correlation analyses did not show any significant correlations between overall speed and the total number of errors (Aware group: S = 1366.3, ρ = −0.19, p = 0.41; Instruction group: S = 1864.8, ρ = −0.052, p = 0.81; Mixed data: S = 13,925, ρ = −0.21, p = 0.18), or between learning efficiency and the total number of errors (Aware group: S = 1216.4, ρ = −0.067, p = 0.78; Instruction group: S = 1824.6, ρ = −0.030, p = 0.89; Mixed data: S = 11,329, ρ = 0.013, p = 0.93).
General discussion
This study examined the effects of manner of acquisition of explicit knowledge, regarding a transfer rule, on transfer of a visuomotor sequence. We found that (1) explicit knowledge of the transfer rule generally led to fewer errors in the transfer session, regardless of how it was acquired (Unaware, 28.00 trials; Aware, 7.52 trials; Instruction, 2.90 trials), (2) the total number of error trials in the transfer session did not differ significantly between the Aware and Instruction groups, (3) explicit knowledge of the instruction led to a slower overall speed than that of spontaneous detection, and (4) the total number of error trials in the transfer session did not contribute to a faster overall speed or better learning efficiency in the transfer session in either the Aware or the Instruction group. These results suggest that explicit knowledge of the transfer rule may have helped reduce errors, irrespective of the manner of acquisition, but it may have interfered with performance speed, particularly when the knowledge was provided, rather than discovered spontaneously.
Hikosaka et al. (1999) proposed a model in which sequential learning is independently acquired by two parallel systems: spatial and motor (see also the neural network model of procedural learning, Nakahara et al. 2001). The spatial system is predominantly involved at the early learning stage (effector-independent learning) and is mostly evaluated by the number of errors committed in a task. The motor system is mainly involved at the late learning stage (effector-dependent learning) and is mostly evaluated by the performance time of a given sequence. In addition, people are capable of developing effector-dependent and effector-independent representations in parallel, but with different time courses (see also Bapi et al. 2000, 2006). Therefore, a shorter performance time in successful trials indicates that participants acquired effector-independent representations earlier and, then, could start to develop effector-dependent representations. The present results show that explicit knowledge can facilitate effector-independent learning, but does not facilitate effector-dependent learning, which is congruent with results of previous studies (e.g., Watanabe et al. 2006). Watanabe et al. (2006) used the 2 × 10 task and rotated the workspace for the transfer session, without notifying participants. The participants who noticed the rules of rotation did not improve performance times compared to those who did not, although they were able to use their explicit knowledge of the rotation to reduce errors. The non-facilitation of effector-dependent learning in the transfer task might arise from two possibilities. One is due to different number of error trials until the first successful trial, reflecting a different working time. Since the Unaware group performed the transfer sequence with trial and error (i.e., greater number of errors), they might have been able to develop larger effector-dependent representations by the first successful trial, compared to the Aware group. In addition to this, the Aware group may have developed effector-dependent representations of the sequence within a shorter time. Therefore, the speed in the Unaware and Aware groups looks similar, but the underlying process is likely different. Alternatively, the results might reflect that explicit knowledge of the transformation rule required cognitive resources, resulting in deactivation of the multidimensional system and activation of only the unidimensional system (Keele et al. 2003). That said, since the number of errors in the transfer task was greatly different between the Aware and Unaware groups (7.52 vs. 28.00 trials), the non-facilitation of speed likely supports the first possibility.
The most significant finding in the present study was that the overall speed of the Instruction group was slower than that of the Aware group, indicating that explicit knowledge provided by another person hindered performance time. This seemed to persist for the entire duration of the experiment. A few qualitatively similar effects were reported previously. An explicit instruction reduced movement errors, but the reduced magnitude of errors caused interference with sensorimotor adaptation (Benson et al. 2011). Performance of well-practiced movements, such as golf putting, can be impaired by explicit instruction (e.g., Beilock and Carr 2001; Flegal and Anderson 2008). As mentioned in the last paragraph, given that explicit knowledge of a transformation rule contributes to the development of speed in the multidimensional system, the most reasonable interpretation is that explicit knowledge provided by instruction requires more cognitive resources in the multidimensional system, compared to that spontaneously discovered. This is supported by the negative improvement in speed in the Instruction group (Fig. 4f). Some studies suggest that explicit instruction leads to an increase of cognitive load (e.g., Masters et al. 2008). Masters et al. (2008) asked novices to learn a table tennis shot with an analogical instruction or explicitly detailed instruction and to do a concurrent low- or high-complexity decision during the shot performance. They observed that performance was disrupted when the participants with the explicit instruction made the high-complexity decision, which indicated that increased cognitive load impaired motor performance. Using an experimental paradigm which is similar to the present study, it has been shown that the frontal areas of the brain are involved in explicit learning and transfer (e.g., Hikosaka et al. 2002; Sakai et al. 1998); the two frontal areas (i.e., the dorsolateral prefrontal cortex and the pre-supplementary motor area) were mainly activated in the earlier stages of learning, and the two parietal areas (i.e., the precuneus and intraparietal sulcus) were mainly activated in the later stages. Then, activity of the frontal areas (i.e., executive function, Miyake et al. 2000) decreases in tasks requiring concurrent task load (e.g., Lavie et al. 2004). Taken together, explicit knowledge provided by another person may automatically require more cognitive resources than those required by spontaneous detection, resulting in learning of the effector-independent sequence to be delayed and, thus, the shift from effector-independent learning to effector-dependent learning also being delayed. In other words, participants who obtained the explicit knowledge via instruction may have taken more time at the effector-independent learning phase.
The present study is the first to directly compare explicit instruction and spontaneous detection and showed that the manner of acquisition of explicit knowledge might play a key role in transfer. That said, the present study has several limitations. One limitation is regarding classification of participants, which was also observed in Curran and Keele (1993). For the Non-instruction group, we classified the participants into the Aware and Unaware groups via interview and found that those in the Aware group had a larger VSWM capacity than those in the Unaware group. However, participants in the Instruction group were not classified by any criteria; therefore, cognitive abilities of participants might not be precisely controlled, even if we did not find a significant difference of VSWM capacity between the Aware and Instruction groups. Another limitation is regarding the role of working memory in the task. In the present study, we adopted only one task in addition to the m × n task. Although we found a significant correlation of sequence learning (i.e., total number of errors) and VSWM capacity, other possibilities could not be ruled out, such as motivation. However, Bo and Seidler (2009) adopted a sequence learning task, visuospatial working memory task, and continuous tapping task, and found that only VSWM capacity was correlated with the rate of motor sequence learning. In addition, since similar neural activation in frontal areas during performances in the earlier learning stage of the m × n task and VSWM task could be assumed (e.g., Hikosaka et al. 2002; Sakai et al. 1998), the present results also likely reflect individual differences of cognitive capacity, not a motivational issue.
References
Abrahamse EL, Jiménez L, Verwey WB, Clegg BA (2010) Representing serial action and perception. Psychon B Rev 17:603–623
Ashby FG, Alfonso-Reese L, Turken A, Waldron E (1998) A neuropsychological theory of multiple-systems in category learning. Psychol Rev 105:442–481
Baguley T (2012) Calculating and graphing within-subject confidence intervals for ANOVA. Behav Res Methods 44:158–175
Bapi RS, Doya K, Harner AM (2000) Evidence for effector independent and dependent representations and their differential time course of acquisition during motor sequence learning. Exp Brain Res 132:149–162
Bapi RS, Miyapuram KP, Graydon FX, Doya K (2006) fMRI investigation of cortical and subcortical networks in the learning of abstract and effector-specific representations of motor sequences. Neuroimage 32:714–727
Beilock SL, Carr TH (2001) On the fragility of skilled performance: what governs choking under pressure? J Exp Psychol Gen 130:701–725
Benson BL, Anguera JA, Seidler RD (2011) A spatial explicit strategy reduces error but interferes with sensorimotor adaptation. J Neurophysiol 105:2843–2851
Bo J, Seidler RD (2009) Visuospatial working memory capacity predicts the organization of acquired explicit motor sequences. J Neurophysiol 101:3116–3125
Bo J, Jennett S, Seidler RD (2011) Working memory capacity correlates with implicit serial reaction time task performance. Exp Brain Res 214:73–81
Curran T, Keele SW (1993) Attentional and nonattentional forms of sequence learning. J Exp Psychol Learn 19:189–202
Dean JRD, Kuhn D (2007) Direct instruction vs. discovery: the long view. Sci Educ 91:384–397
Flegal KE, Anderson MC (2008) Overthinking skilled motor performance: or why those who teach can not do. Psychon B Rev 15:927–932
Gabrieli JD, Corkin S, Mickel SF, Growdon JH (1993) Intact acquisition and long-term retention of mirror-tracing skill in Alzheimer’s disease and in global amnesia. Behav Neurosci 107:899–910
Grafton ST, Hazeltine E, Ivry R (1995) Functional mapping of sequence learning in normal humans. J Cogn Neurosci 7:497–510
Hazeltine E, Grafton ST, Ivry R (1997) Attention and stimulus characteristics determine the locus of motor sequence encoding: a PET study. Brain 120:123–140
Heindel WC, Salmon DP, Shults CW, Walicke PA, Butters N (1989) Neuropsychological evidence for multiple implicit memory systems: a comparison of Alzheimer’s, Huntington’s, and Parkinson’s disease patients. J Neurosci 9:582–587
Hikosaka O, Rand MK, Miyachi S, Miyashita K (1995) Learning of sequential movements in the monkey: process of learning and retention of memory. J Neurophysiol 74:1652–1661
Hikosaka O, Sakai K, Miyauchi S, Takino R, Sasaki Y, Putz B (1996) Activation of human presupplementary motor area in learning of sequential procedures: a functional MRI study. J Neurophysiol 76:617–621
Hikosaka O, Nakahara H, Rand MK, Sakai K, Lu X, Nakamura K, Miyachi S et al (1999) Parallel neural networks for learning sequential procedures. Trends Neurosci 22:464–471
Hikosaka O, Nakamura K, Sakai K, Nakahara H (2002) Central mechanisms of motor skill learning. Curr Opin Neurobiol 12:217–222
Keele SW, Ivry R, Mayr U, Hazeltine E, Heuer H (2003) The cognitive and neural architecture of sequence representation. Psychol Rev 110:316–339
Klahr D, Nigam M (2004) The equivalence of learning paths in early science instruction effects of direct instruction and discovery learning. Psychol Sci 15:661–667
Lavie N, Hirst A, de Fockert JW, Viding E (2004) Load theory of selective attention and cognitive control. J Exp Psychol Gen 133:339–354
Luck SJ, Vogel EK (1997) The capacity of visual working memory for features and conjunctions. Nature 390:279–281
Malone LA, Bastian AJ (2010) Thinking about walking: effects of conscious correction versus distraction on locomotor adaptation. J Neurophysiol 103:1954–1962
Masters RSW, Poolton JM, Maxwell JP, Raab M (2008) Implicit motor learning and complex decision making in time-constrained environments. J Motor Behav 40:71–79
Miyake A, Friedman NP, Emerson MJ, Witzki AH, Howerter A, Wager TD (2000) The unity and diversity of executive functions and their contributions to complex “frontal lobe” tasks: a latent variable analysis. Cognitive Psychol 41:49–100
Nakahara H, Doya K, Hikosaka O (2001) Parallel cortico-basal ganglia mechanisms for acquisition and execution of visuomotor sequences—a computational approach. J Cognitive Neurosci 13:626–647
Nissen MJ, Bullemer P (1987) Attentional requirements of learning: evidence from performance measures. Cogn Psychol 19:1–32
Sakai K, Hikosaka O, Miyachi S, Takino R, Sasaki Y, Putz B (1998) Transition of brain activation from frontal to parietal areas in visuomotor sequence learning. J Neurosci 18:1877–1840
Sakai K, Kitaguchi K, Hikosaka O (2003) Chunking during human visuomotor learning. Exp Brain Res 152:229–242
Sakai K, Hikosaka O, Nakamura K (2004) Emergence of rhythm during motor learning. Trends Cogn Sci 8:547–553
Speelman CP, Kirsner K (2005) Beyond the learning curve: the construction of mind. Oxford University Press, Oxford
Stefaniak N, Willems S, Adam S, Meulemans T (2008) What is the impact of the explicit knowledge of sequence regularities on both deterministic and probabilistic serial reaction time task performance? Mem Cogn 36:1283–1298
Tanaka K, Watanabe K (2013) Effects of learning with explicit elaboration on implicit transfer of visuomotor sequence learning. Exp Brain Res 228:411–425
Tanaka K, Watanabe K (2014a) Implicit transfer of reversed temporal structure in visuomotor sequence learning. Acta Psychol 153:1–12
Tanaka K, Watanabe K (2014b) Implicit transfer of reversed temporal structure in visuomotor sequence learning. Cogn Sci 38:565–579
Tanaka K, Watanabe K (2016) Impacts of visuomotor sequence learning methods on speed and accuracy: starting over from the beginning or from the point of error. Acta Psychol 164:169–180
Vogel EK, Machizawa MG (2004) Neural activity predicts individual differences in visual working memory capacity. Nature 428:748–751
Watanabe K, Ikeda H, Hikosaka O (2006) Effects of explicit knowledge of workspace rotation in visuomotor sequence learning. Exp Brain Res 174:673–678
Watanabe K, Ikeda H, Miyao M (2010) Learning efficacy of explicit visuomotor sequences in children with attention-deficit/hyperactivity disorder and Asperger syndrome. Exp Brain Res 203:233–239
Werner S, Bock O (2007) Effects of variable practice and declarative knowledge on sensorimotor adaptation to rotated visual feedback. Exp Brain Res 178:554–559
Willingham DB, Salidis J, Gabrieli JD (2002) Direct comparison of neural systems mediating conscious and unconscious skill learning. J Neurophysiol 88:1451–1460
Ziori E, Dienes Z (2006) Subjective measures of unconscious knowledge of concepts. Mind Society 5:105–122
Ziori E, Dienes Z (2008) How does prior knowledge affect implicit and explicit concept learning? Q J Exp Psychol 61:601–624
Acknowledgements
This work was supported by a Grant-in-Aid for Young Scientists (20727086) to KT and CREST, Japan Science and Technology Agency to KW. The preliminary results of the present study were presented in the 34th annual meeting of the Cognitive Science Society: Tanaka, K., & Watanabe, K. (2012) Effects of explicit knowledge on transfer of visuomotor sequence learning. In N. Miyake, D. Peebles, & R. P. Cooper (Eds.), Proceedings of the 34th Annual Conference of the Cognitive Science Society, 1036–1041. Austin, TX: Cognitive Science Society. ISBN 978-0-9768318-8-4.
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All authors developed the study concept and contributed to the study design. Testing and data collection were performed by K. Tanaka. He also performed the data analysis and interpretation under the supervision of K. Watanabe and drafted the manuscript, and K. Watanabe provided critical revisions. All authors approved the final version of the manuscript for submission.
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Tanaka, K., Watanabe, K. Explicit instruction of rules interferes with visuomotor skill transfer. Exp Brain Res 235, 1689–1700 (2017). https://doi.org/10.1007/s00221-017-4933-4
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DOI: https://doi.org/10.1007/s00221-017-4933-4