The stuff that motor chunks are made of: Spatial instead of motor representations?
Identifieur interne : 003D05 ( Ncbi/Merge ); précédent : 003D04; suivant : 003D06The stuff that motor chunks are made of: Spatial instead of motor representations?
Auteurs : Willem B. Verwey [Pays-Bas, États-Unis] ; Eduard C. Groen [Pays-Bas, Allemagne] ; David L. Wright [États-Unis]Source :
- Experimental Brain Research [ 0014-4819 ] ; 2015.
Abstract
In order to determine how participants represent practiced, discrete keying sequences in the discrete sequence production task, we had 24 participants practice two six-key sequences on the basis of two pre-learned six-digit numbers. These sequences were carried out by fingers of the left (L) and right (R) hand with between-hand transitions always occurring between the second and third, and the fifth and sixth responses. This yielded the so-called LLRRRL and RRLLLR sequences. Early and late in practice, the keypad used for the right hand was briefly relocated from the front of the participants to 90° at their right side. The results indicate that after 600 practice trials, executing a keying sequence relies heavily on a spatial cross-hand representation in a trunk- or head-based reference frame that after about only 15 trials is fully adjusted to the changed hand location. The hand location effect was not found with the last sequence element. This is attributed to the application of explicit knowledge. The between-hand transitions appeared to induce initial segmentation in some of the participants, but this did not consolidate into a concatenation point of successive motor chunks.
Url:
DOI: 10.1007/s00221-015-4457-8
PubMed: 26487177
PubMed Central: 4731443
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PMC:4731443Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>In order to determine how participants represent practiced, discrete keying sequences in the discrete sequence production task, we had 24 participants practice two six-key sequences on the basis of two pre-learned six-digit numbers. These sequences were carried out by fingers of the left (L) and right (R) hand with between-hand transitions always occurring between the second and third, and the fifth and sixth responses. This yielded the so-called LLRRRL and RRLLLR sequences. Early and late in practice, the keypad used for the right hand was briefly relocated from the front of the participants to 90° at their right side. The results indicate that after 600 practice trials, executing a keying sequence relies heavily on a spatial cross-hand representation in a trunk- or head-based reference frame that after about only 15 trials is fully adjusted to the changed hand location. The hand location effect was not found with the last sequence element. This is attributed to the application of explicit knowledge. The between-hand transitions appeared to induce initial segmentation in some of the participants, but this did not consolidate into a concatenation point of successive motor chunks.</p>
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</TEI>
<pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Exp Brain Res</journal-id>
<journal-id journal-id-type="iso-abbrev">Exp Brain Res</journal-id>
<journal-title-group><journal-title>Experimental Brain Research</journal-title>
</journal-title-group>
<issn pub-type="ppub">0014-4819</issn>
<issn pub-type="epub">1432-1106</issn>
<publisher><publisher-name>Springer Berlin Heidelberg</publisher-name>
<publisher-loc>Berlin/Heidelberg</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">26487177</article-id>
<article-id pub-id-type="pmc">4731443</article-id>
<article-id pub-id-type="publisher-id">4457</article-id>
<article-id pub-id-type="doi">10.1007/s00221-015-4457-8</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>The stuff that motor chunks are made of: Spatial instead of motor representations?</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">http://orcid.org/0000-0003-3994-8854</contrib-id>
<name><surname>Verwey</surname>
<given-names>Willem B.</given-names>
</name>
<address><phone>++31-53- 489 3611/4764</phone>
<email>w.b.verwey@utwente.nl</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
<xref ref-type="aff" rid="Aff2"></xref>
<xref ref-type="aff" rid="Aff4"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Groen</surname>
<given-names>Eduard C.</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
<xref ref-type="aff" rid="Aff3"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Wright</surname>
<given-names>David L.</given-names>
</name>
<xref ref-type="aff" rid="Aff2"></xref>
</contrib>
<aff id="Aff1"><label></label>
MIRA Research Institute, University of Twente, Enschede, The Netherlands</aff>
<aff id="Aff2"><label></label>
Human Performance Laboratories, Department of Health and Kinesiology, Texas A&M University, College Station, TX USA</aff>
<aff id="Aff3"><label></label>
Fraunhofer Institute for Experimental Software Engineering, Kaiserslautern, Germany</aff>
<aff id="Aff4"><label></label>
Department of Cognitive Psychology and Ergonomics, University of Twente, PO Box 217, 7500 AE Enschede, The Netherlands</aff>
</contrib-group>
<pub-date pub-type="epub"><day>20</day>
<month>10</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>20</day>
<month>10</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="ppub"><year>2016</year>
</pub-date>
<volume>234</volume>
<fpage>353</fpage>
<lpage>366</lpage>
<history><date date-type="received"><day>27</day>
<month>5</month>
<year>2015</year>
</date>
<date date-type="accepted"><day>25</day>
<month>9</month>
<year>2015</year>
</date>
</history>
<permissions><copyright-statement>© The Author(s) 2015</copyright-statement>
<license license-type="OpenAccess"><license-p><bold>Open Access</bold>
This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.</license-p>
</license>
</permissions>
<abstract id="Abs1"><p>In order to determine how participants represent practiced, discrete keying sequences in the discrete sequence production task, we had 24 participants practice two six-key sequences on the basis of two pre-learned six-digit numbers. These sequences were carried out by fingers of the left (L) and right (R) hand with between-hand transitions always occurring between the second and third, and the fifth and sixth responses. This yielded the so-called LLRRRL and RRLLLR sequences. Early and late in practice, the keypad used for the right hand was briefly relocated from the front of the participants to 90° at their right side. The results indicate that after 600 practice trials, executing a keying sequence relies heavily on a spatial cross-hand representation in a trunk- or head-based reference frame that after about only 15 trials is fully adjusted to the changed hand location. The hand location effect was not found with the last sequence element. This is attributed to the application of explicit knowledge. The between-hand transitions appeared to induce initial segmentation in some of the participants, but this did not consolidate into a concatenation point of successive motor chunks.</p>
</abstract>
<kwd-group xml:lang="en"><title>Keywords</title>
<kwd>Cognitive models</kwd>
<kwd>Motor control</kwd>
<kwd>Sequence learning</kwd>
<kwd>Motor chunking</kwd>
<kwd>Spatial reference frames</kwd>
</kwd-group>
<custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name>
<meta-value>© Springer-Verlag Berlin Heidelberg 2016</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body><sec id="Sec1" sec-type="introduction"><title>Introduction</title>
<p>A large number of studies has been devoted to understanding how humans automate movement sequences like writing one’s signature and shifting gears when driving an automobile (for recent reviews, see, e.g., Abrahamse et al. <xref ref-type="bibr" rid="CR1">2010</xref>
, <xref ref-type="bibr" rid="CR2">2013</xref>
; Heuer and Massen <xref ref-type="bibr" rid="CR29">2013</xref>
; Keele et al. <xref ref-type="bibr" rid="CR36">2003</xref>
; Shea and Kovacs <xref ref-type="bibr" rid="CR74">2013</xref>
; Verwey et al. <xref ref-type="bibr" rid="CR95">2015</xref>
). Automating movement sequences allow individuals to devote most of their processing resources to concurrent tasks and/or prepare for upcoming behavior while they are executing a familiar movement pattern. To study the human capacity to automate movement sequences, researchers have developed various laboratory tasks that allow them to distinguish the various cognitive processes and representations underlying skilled movement execution. These tasks include, among others, sequential aiming tasks like the flexion–extension (FE) task (Panzer et al. <xref ref-type="bibr" rid="CR56">2006</xref>
) and sequential key pressing tasks like the serial reaction time (RT) task (Nissen and Bullemer <xref ref-type="bibr" rid="CR54">1987</xref>
) and the presently used <italic>discrete sequence production</italic>
(DSP) task (Abrahamse et al. <xref ref-type="bibr" rid="CR2">2013</xref>
; Verwey <xref ref-type="bibr" rid="CR83">1999</xref>
). Research with tasks like these have made a strong case that sequential motor learning involves the simultaneous development and use of various task- and practice-dependent representations (Berniker et al. <xref ref-type="bibr" rid="CR12">2014</xref>
; Keele et al. <xref ref-type="bibr" rid="CR35">1995</xref>
; Panzer et al. <xref ref-type="bibr" rid="CR57">2014</xref>
; Proteau and Carnahan <xref ref-type="bibr" rid="CR64">2001</xref>
; Shea and Kovacs <xref ref-type="bibr" rid="CR74">2013</xref>
; Shea et al. <xref ref-type="bibr" rid="CR75">2011</xref>
; Verwey et al. <xref ref-type="bibr" rid="CR95">2015</xref>
; Wiestler et al. <xref ref-type="bibr" rid="CR96">2014</xref>
). Representing movement sequences in such a redundant way allows human motor control to be flexibly adjusted to changes in the environment and the effectors being used, as well as deal with the detrimental effects on serial behavior of aging and neural damage.</p>
<p>In the laboratory, movement order in sequence learning tasks is usually guided by a series of stimuli, each indicating an element of the sequence. Consequently, sequences in these tasks are initially produced in the <italic>reaction mode</italic>
(Abrahamse et al. <xref ref-type="bibr" rid="CR2">2013</xref>
; Hikosaka et al. <xref ref-type="bibr" rid="CR30">1999</xref>
; Park and Shea <xref ref-type="bibr" rid="CR59">2005</xref>
; Verwey <xref ref-type="bibr" rid="CR85">2003</xref>
). As the movement sequence is repeated, regularities in the order of the movements—and the associated stimuli—are gradually learned at all levels of information processing (Abrahamse et al. <xref ref-type="bibr" rid="CR1">2010</xref>
; Verwey et al. <xref ref-type="bibr" rid="CR95">2015</xref>
). With limited practice, participants still need external guidance to produce the sequence, but the successive processes and movements are already primed using the <italic>associative mode</italic>
(Verwey and Abrahamse <xref ref-type="bibr" rid="CR87">2012</xref>
; also see Ruitenberg et al. <xref ref-type="bibr" rid="CR70">2014</xref>
; Verwey and Wright <xref ref-type="bibr" rid="CR92">2014</xref>
). The associative mode is assumed to be responsible for the skill that develops in the serial RT task.</p>
<p>When movement sequences are limited to about 5–8 elements, as is typically the case for the DSP task (Abrahamse et al. <xref ref-type="bibr" rid="CR2">2013</xref>
), they can be planned before being executed. This allows strategies to develop and use effective representations (Henry and Rogers <xref ref-type="bibr" rid="CR28">1960</xref>
; Sternberg et al. <xref ref-type="bibr" rid="CR79">1978</xref>
; Verwey <xref ref-type="bibr" rid="CR82">1996</xref>
). Consequently, with further practice, the need for perceptual and central processing resources to translate individual stimuli (S) into responses (Rs) reduces because sequence-specific representations develop that are called <italic>motor chunks</italic>
, and that rely on R–R associations. These motor chunks allow sequence execution to occur without external guidance in the so-called <italic>chunking mode</italic>
(Abrahamse et al. <xref ref-type="bibr" rid="CR2">2013</xref>
; Verwey and Abrahamse <xref ref-type="bibr" rid="CR87">2012</xref>
). Like memory chunks in general (Halford et al. <xref ref-type="bibr" rid="CR27">1998</xref>
; Miller <xref ref-type="bibr" rid="CR50">1956</xref>
; Newell and Rosenbloom <xref ref-type="bibr" rid="CR52">1981</xref>
), motor chunks help bypass limitations in information processing so that short movement series can be selected, prepared, and executed as if they constitute a single response (Verwey <xref ref-type="bibr" rid="CR83">1999</xref>
). While the motor chunk construct is generally accepted, it is defined by its behavioral properties, and despite its name, it remains unclear as to how motor chunks code the individual movements of the DSP task (Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
). This is the central issue in the present paper.</p>
<sec id="Sec2"><title>Sequence representations</title>
<p>The recently proposed cognitive framework for sequential motor behavior (C-SMB; Verwey et al. <xref ref-type="bibr" rid="CR95">2015</xref>
) postulates that the repeated execution of movement sequences induces the development of a number of different representations some of which may underlie motor chunks. In keeping with the general notion that with practice perceptual motor skills become increasingly task-specific (Ackerman <xref ref-type="bibr" rid="CR4">1988</xref>
; Fleishman and Hempel <xref ref-type="bibr" rid="CR24">1955</xref>
; Newell and Rosenbloom <xref ref-type="bibr" rid="CR52">1981</xref>
; Proteau et al. <xref ref-type="bibr" rid="CR65">1992</xref>
), C-SMB assumes that, first, S-R associations develop that allow a central processor to perform in the reaction mode. With limited practice, <italic>central</italic>
-<italic>symbolic</italic>
(e.g., spatial and/or verbal) representations develop that can be parsed by the central processor in a cognitive loop. Central-symbolic representations may involve various ways of coding the sequence, such as a visual–spatial image of the required actions (relying on episodic memory), the numbers of one’s PIN (using verbal memory), and/or a spatial representation of successive target locations (spatial memory). This type of knowledge can probably be verbally expressed and is assumed to contribute heavily to what has been called explicit sequence knowledge. Given the abstract level of this knowledge, it is independent of the effector system being used.</p>
<p>Spatial representations of the successive movements are assumed to develop more slowly than the verbal representations that are stored in episodic memory (Shea et al. <xref ref-type="bibr" rid="CR75">2011</xref>
; Witt et al. <xref ref-type="bibr" rid="CR100">2008</xref>
). However, during sequence execution, these spatial representations require less cognitive processing than verbal descriptions because spatial representations provide information that can directly be used for planning each individual movement. Inspired by findings with single-cell recordings, behavioral research has explored the nature of these spatial representations in various tasks. That research confirmed neurophysiological indications for a variety of spatial reference frames in which movements can be coded (Flanders and Soechting <xref ref-type="bibr" rid="CR23">1995</xref>
; Shea et al. <xref ref-type="bibr" rid="CR75">2011</xref>
; Wiestler et al. <xref ref-type="bibr" rid="CR96">2014</xref>
). That is, the spatial coordinates of individual movement endpoints may be relative to objects in the person’s environment (they are then coded in an <italic>allocentric reference frame</italic>
), but also relative to body parts like the eye, head, shoulder, trunk, forearm, and hand (i.e., involving <italic>egocentric reference frames</italic>
, Bernier and Grafton <xref ref-type="bibr" rid="CR11">2010</xref>
; Colby and Goldberg <xref ref-type="bibr" rid="CR18">1999</xref>
; Gentilucci et al. <xref ref-type="bibr" rid="CR25">1996</xref>
; Krakauer et al. <xref ref-type="bibr" rid="CR43">1999</xref>
; Obhi and Goodale <xref ref-type="bibr" rid="CR55">2005</xref>
; Shea et al. <xref ref-type="bibr" rid="CR75">2011</xref>
; Zacks <xref ref-type="bibr" rid="CR102">2008</xref>
).</p>
<p>Allocentric representations have been argued to support strategic, goal-oriented processes that are effector independent. Egocentric reference frames are important for executing motor sequences (Willingham <xref ref-type="bibr" rid="CR98">1998</xref>
), may include effector-dependent and effector-independent components (Wiestler et al. <xref ref-type="bibr" rid="CR96">2014</xref>
), and are associated with other brain networks than allocentric representations (Zacks <xref ref-type="bibr" rid="CR102">2008</xref>
). It is generally believed now that sequential motor tasks involve the simultaneous use of spatial representations with varying reference frames (Keulen et al. <xref ref-type="bibr" rid="CR39">2002</xref>
; Leoné et al. <xref ref-type="bibr" rid="CR45">2015</xref>
; McIntyre et al. <xref ref-type="bibr" rid="CR49">1998</xref>
). Activating a particular movement goal and action plan would automatically activate the spatial representations needed for executing a sequencing task (Jeannerod <xref ref-type="bibr" rid="CR31">1997</xref>
). The contributions of the various reference frames can probably also be modulated intentionally (Abrams and Landgraf <xref ref-type="bibr" rid="CR3">1990</xref>
; Proctor et al. <xref ref-type="bibr" rid="CR63">2004</xref>
), which might be useful when the movement sequence is carried out in different spatial contexts. Neurophysiological measurements indicate that various brain regions can host different reference frames simultaneously. Also, one reference frame can be replaced by another within less than about 100 ms (Derdikman and Moser <xref ref-type="bibr" rid="CR22">2010</xref>
; Zacks <xref ref-type="bibr" rid="CR102">2008</xref>
), which may be associated with the ability to rotate spatial representations (Georgopoulos et al. <xref ref-type="bibr" rid="CR26">1986</xref>
; Leoné et al. <xref ref-type="bibr" rid="CR45">2015</xref>
; Pellizzer et al. <xref ref-type="bibr" rid="CR60">2009</xref>
; Petit et al. <xref ref-type="bibr" rid="CR61">2003</xref>
; Shepard and Metzler <xref ref-type="bibr" rid="CR76">1971</xref>
).</p>
<p>According to C-SMB, extensive practice of a sequential motor task would introduce the use of <italic>motor</italic>
representations that are carried out by the motor processor. This type of representation is called motoric because it would entail activation patterns of agonist/antagonist muscles (Shea et al. <xref ref-type="bibr" rid="CR75">2011</xref>
), musculoskeletal forces and dynamics (Krakauer et al. <xref ref-type="bibr" rid="CR43">1999</xref>
), joint angles (Criscimagna-Hemminger et al. <xref ref-type="bibr" rid="CR20">2003</xref>
), posture-related representations (Rosenbaum et al. <xref ref-type="bibr" rid="CR67">2009</xref>
; Rosenbaum et al. <xref ref-type="bibr" rid="CR66">1999</xref>
), and/or the orientation of body segments relative to each other (Lange et al. <xref ref-type="bibr" rid="CR44">2004</xref>
). Despite the varying terminology, these notions all suggest that a sequence representation is developed in terms of muscles or muscle groups (cf. Keele <xref ref-type="bibr" rid="CR34">1968</xref>
). Due to their motoric coding, these representations require little processing to execute a sequence and allow rapid sequence execution by the motor processor without relying very much on the central processor (Verwey et al. <xref ref-type="bibr" rid="CR95">2015</xref>
). These motor representations are not accessible to processes involved in awareness, that is, motor representations are implicit (though people may still have independent explicit knowledge too, Jeannerod <xref ref-type="bibr" rid="CR31">1997</xref>
).</p>
<p>There now seems some consensus that the various representations underlying motor sequencing skill develop at different processing levels and that each representation can contribute to the execution of individual movements. Even central-symbolic codes—like verbal ones—and reacting to guiding stimuli are believed to contribute to the execution of highly practiced motor sequences (Keisler and Shadmehr <xref ref-type="bibr" rid="CR37">2010</xref>
; Kovacs et al. <xref ref-type="bibr" rid="CR42">2009</xref>
; Stanley and Krakauer <xref ref-type="bibr" rid="CR78">2013</xref>
; Verwey <xref ref-type="bibr" rid="CR83">1999</xref>
). In DSP sequences, these central-symbolic representations may speed up especially those sequence elements that are executed more slowly (Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
). Furthermore, due to primacy and recency effects in memory (Bonanni et al. <xref ref-type="bibr" rid="CR15">2007</xref>
; Johnson <xref ref-type="bibr" rid="CR32">1991</xref>
), the speedup by explicit knowledge can be expected especially for the elements at the sequence start and end. Using Monte Carlo simulations, Verwey (<xref ref-type="bibr" rid="CR85">2003</xref>
) showed that simultaneous activity of independent parallel processing systems—each potentially using another representation—increases execution rate as long as there is an overlap in the distributions of the times it takes each system to trigger a response. A racing processor mechanism appears to be a general feature of information processing as it underlies also models of simple RT, response selection, and the processing of redundant signals (Cho and Proctor <xref ref-type="bibr" rid="CR17">2002</xref>
; Logan <xref ref-type="bibr" rid="CR46">1988</xref>
; Logan et al. <xref ref-type="bibr" rid="CR47">2014</xref>
; Miller and Ulrich <xref ref-type="bibr" rid="CR51">2003</xref>
; Nicoletti et al. <xref ref-type="bibr" rid="CR53">1984</xref>
; Proctor and Reeve <xref ref-type="bibr" rid="CR62">1988</xref>
; Ulrich and Miller <xref ref-type="bibr" rid="CR80">1997</xref>
). Behavioral support for the idea that executing familiar movement sequences involves a race between (processors using) different representations comes from the finding that individual participants had two or three peaks in their RT distribution when they changed from the reaction to the chunking mode (Verwey <xref ref-type="bibr" rid="CR85">2003</xref>
). This suggests that for some trials, the fastest of several different representations was not applied, and a less efficient one was used to trigger the appropriate sequence element.</p>
<p>The conclusion in behavioral studies that a motor representation developed is usually based on the slowing that is observed when a highly practiced sequence is executed with another effector (e.g., Andresen and Marsolek <xref ref-type="bibr" rid="CR8">2012</xref>
; Park and Shea <xref ref-type="bibr" rid="CR59">2005</xref>
; Verwey and Clegg <xref ref-type="bibr" rid="CR88">2005</xref>
; Verwey and Wright <xref ref-type="bibr" rid="CR91">2004</xref>
). Such a motor representation should make execution skill independent of the location in which the effector is being used. However, location-independent sequence execution contrasts with the idea that practice makes perceptuomotor skills increasingly task (and thus location) specific (Ackerman <xref ref-type="bibr" rid="CR4">1988</xref>
; Fleishman and Hempel <xref ref-type="bibr" rid="CR24">1955</xref>
; Proteau et al. <xref ref-type="bibr" rid="CR65">1992</xref>
). In this context, it is interesting that De Kleine and Verwey (<xref ref-type="bibr" rid="CR21">2009</xref>
) found that the speed advantage of the practiced over the unpracticed hand in a DSP task reduced when the practiced hand was located on the other side of the participants’ body. This suggests that the advantage of the practiced over the unpracticed hand cannot always be attributed to a motor (muscle-specific) representation and may instead involve a spatial representation that is both effector specific and sensitive to the location of the hand.</p>
<p>The main goal of the present study was to examine bimanual keying sequences in the DSP task to determine the representations underlying sequencing skill earlier and later in practice. To that end, participants practiced a discrete keying sequence with fingers of both hands while the hands were in the normal adjacent position in front of the body. They then relocated the right hand to the side while the left hand remained in its usual location in front of the trunk (like a 1970s or 1980s musician playing on two keyboards at the same time). According to what will be referred to as the <italic>applicability hypothesis</italic>
, participants switch off inappropriate representations when their hand is in a novel location. When in that situation, the most applicable representations are hand-based (i.e., muscle-oriented and/or with a hand-based reference frame), and execution rate will suffer little. An alternative account is called the <italic>adjustment hypothesis</italic>
. It assumes that with practice, execution is based on highly task-specific sequence representations that can be fine-tuned for a particular task. So, rather than switching off inappropriate representations, representations are adjusted to accommodate a changed hand location, for example, by rotating a spatial representation of the sequence (Shepard and Metzler <xref ref-type="bibr" rid="CR76">1971</xref>
).</p>
</sec>
<sec id="Sec3"><title>Chunk boundaries</title>
<p>Another issue in the present study concerns many indications that movement sequences exceeding about 3–5 elements include multiple motor chunks (Acuna et al. <xref ref-type="bibr" rid="CR5">2014</xref>
; Bo and Seidler <xref ref-type="bibr" rid="CR13">2009</xref>
; Kornbrot <xref ref-type="bibr" rid="CR41">1989</xref>
; Kovacs et al. <xref ref-type="bibr" rid="CR42">2009</xref>
; Verwey and Eikelboom <xref ref-type="bibr" rid="CR90">2003</xref>
; Wymbs et al. <xref ref-type="bibr" rid="CR101">2012</xref>
). The prime indicator that a motor chunk is used consists of a relatively slow response followed by several relatively fast responses (Bo et al. <xref ref-type="bibr" rid="CR14">2009</xref>
; Bo and Seidler <xref ref-type="bibr" rid="CR13">2009</xref>
; Kennerley et al. <xref ref-type="bibr" rid="CR38">2004</xref>
; Ruitenberg et al. <xref ref-type="bibr" rid="CR69">2013</xref>
; Ruitenberg et al. <xref ref-type="bibr" rid="CR71">2015</xref>
; for a test of various indicators of motor chunks, see Verwey <xref ref-type="bibr" rid="CR84">2001</xref>
). The estimate of 3–5 elements per motor chunk in discrete keying sequences is remarkably similar to the chunk size for verbal and visuospatial knowledge of 3–4 in working memory (Anderson <xref ref-type="bibr" rid="CR7">2014</xref>
; Broadbent <xref ref-type="bibr" rid="CR16">1975</xref>
; Cowan <xref ref-type="bibr" rid="CR19">2000</xref>
; Logie and Cowan <xref ref-type="bibr" rid="CR48">2015</xref>
). One could therefore hypothesize that the initial segmentation<xref ref-type="fn" rid="Fn1">1</xref>
of a longer sequence is determined by working-memory capacity and that practice then consolidates these segments into successive motor chunks. Support for this hypothesis comes from studies showing correlations between individual visuospatial working-memory capacity and motor chunk length (Bo et al. <xref ref-type="bibr" rid="CR14">2009</xref>
; Bo and Seidler <xref ref-type="bibr" rid="CR13">2009</xref>
; Seidler et al. <xref ref-type="bibr" rid="CR73">2012</xref>
). While the number of elements per motor chunk does indeed seem to be a prime determinant of where these transitions occur (Abrahamse et al. <xref ref-type="bibr" rid="CR2">2013</xref>
), other sequence properties may influence the sequential position of this so-called <italic>concatenation point</italic>
. Those properties include regularities in the order of the elements (like 123123, De Kleine and Verwey <xref ref-type="bibr" rid="CR21">2009</xref>
; Jones <xref ref-type="bibr" rid="CR33">1981</xref>
; Koch and Hoffmann <xref ref-type="bibr" rid="CR40">2000</xref>
; Kornbrot <xref ref-type="bibr" rid="CR41">1989</xref>
; Sakai et al. <xref ref-type="bibr" rid="CR72">2003</xref>
; Verwey and Eikelboom <xref ref-type="bibr" rid="CR90">2003</xref>
), the use of random versus blocked practice schedules (Wilde et al. <xref ref-type="bibr" rid="CR97">2005</xref>
), and the occurrence of a pause at a particular sequential position during practice (Stadler <xref ref-type="bibr" rid="CR77">1993</xref>
; Verwey <xref ref-type="bibr" rid="CR82">1996</xref>
; Verwey et al. <xref ref-type="bibr" rid="CR93">2009</xref>
; Verwey and Dronkert <xref ref-type="bibr" rid="CR89">1996</xref>
).</p>
<p>The occurrence in the present study of between-hand transitions at two fixed sequential positions allowed us to examine the suggestion by Verwey and Eikelboom (<xref ref-type="bibr" rid="CR90">2003</xref>
) that such transitions might in unfamiliar sequences determine segmentation, which then consolidates with practice into the more robust motor chunks. This idea received some support from the finding with unfamiliar keying sequences that six of the eight observed slow elements in a DSP sequence were associated with a between-hand transition (Verwey et al. <xref ref-type="bibr" rid="CR93">2009</xref>
). A lasting effect of between-hand transitions in DSP sequences would be consistent with the development of hand-specific sequence representations in the serial RT task (Berner and Hoffmann <xref ref-type="bibr" rid="CR9">2008</xref>
, <xref ref-type="bibr" rid="CR10">2009</xref>
) and with indications that fingers of one hand can be prepared by a neural system (a network including the basal ganglia), which differs from the one used for two hands (Adam et al. <xref ref-type="bibr" rid="CR6">2003</xref>
). The question whether between-hand transitions contribute to dividing a keying sequence into different segments in early practice, that may consolidate with practice into the more robust motor chunks, has not been addressed in earlier DSP studies because those studies involved sequence elements being balanced across fingers of different participants, so that between-hand transitions were distributed across all sequential positions.</p>
</sec>
<sec id="Sec4"><title>The present experiment</title>
<p>The applicability and the adjustment hypotheses were tested by having participants first practice two six-element DSP sequences with both hands in the typical adjacent frontal location and then examining the effect on the individual sequence elements of relocating the right hand to the side. This was done after approximately 100 and 600 practice trials per sequence. The applicability hypothesis predicts that all sequence elements are slowed when one hand has been relocated because one or more sequence representations are no longer used. This slowing should not change significantly during a test block because new sequence representations do not develop very fast. In contrast, the adjustment hypothesis predicts that the slowing caused by relocating one hand to the side may last for just a few trials because participants quickly learn to apply a transformation to the representations used (like when rotating a spatial representation). This slowing should occur before the first of the responses given by a particular hand because (the representations making up) motor chunks are adjusted before they can be used. Because practice execution is based on fewer, more sequence-specific, representations (Ackerman <xref ref-type="bibr" rid="CR4">1988</xref>
; Fleishman and Hempel <xref ref-type="bibr" rid="CR24">1955</xref>
; Newell and Rosenbloom <xref ref-type="bibr" rid="CR52">1981</xref>
; Proteau et al. <xref ref-type="bibr" rid="CR65">1992</xref>
), indications for such an adjustment of representations are expected to be stronger in Block 9 than in Block 2. We also assessed awareness of the sequences to determine whether explicit sequence knowledge may contribute to sequence execution. In discrete keying sequence, this may concern especially the second and last responses (i.e., R<sub>2</sub>
and R<sub>6</sub>
, Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
). Finally, we addressed in the conditions in which the right hand was in the front, whether the between-hand transitions might influence the segmentation of each sequence in early practice, and whether this would consolidate with practice when motor chunks develop.</p>
</sec>
</sec>
<sec id="Sec5" sec-type="materials|methods"><title>Method</title>
<sec id="Sec6"><title>Participants</title>
<p>Twenty-four students (16 female, M age = 21 years, SD = 2.0 years) from the University of Twente took part in this study in exchange for course credit. All participants were self-proclaimed right-handed students. Informed consent was obtained from all individual participants included in the study. The study had been approved by the Ethics Committee of the University of Twente and was performed in accordance with the ethical standards described in the Declaration of Helsinki.</p>
</sec>
<sec id="Sec7"><title>Apparatus</title>
<p>The experiment was programmed and conducted in E-Prime 2.0 on a 2.8 GHz Pentium 4 PC with 512 MB RAM running under Windows XP. Key-specific stimuli consisted of eight squares that subtended a visual angle of approximately 1°. They were presented on a 15″ Philips 107T5 CRT display at a refresh rate of 75 Hz, with a resolution of 640 × 480 pixels, and at 16-bit color depth.</p>
<p>Directly in front of the participant were two Trust USB numeric keypads, embedded near each other in a black wooden mold (see Fig. <xref rid="Fig1" ref-type="fig">1</xref>
). In this frontal location, the left keypad was itself rotated 90° counterclockwise, the one on the right 90° clockwise. This allowed participants to place their left hand’s little, ring, middle, and index fingers on the left keypad’s “/,” “8,” “5,” and “2” keys, respectively, and their right hand’s index, middle, ring and little fingers on the right keypad’s “3,” “6,” “9,” and “*” keys, respectively. Connecting these two identical keypads via the same USB controller in the computer induced negligible delays (USB 2.0 delays signals by about 8 ms). The dual keypad setup was chosen so that the hands were placed as close together as possible during the practice phase, while in the test phase the right-hand keypad could be relocated without a possible confound with using different keypads. Because participants had their head in a chinrest, the keypad located at the side of the participant was outside the participants’ field of view. To prevent confounding of keypad location and sight at the keypads in the frontal location, we occluded the participants’ sight for the frontal keypad location with a black letter tray. In one of the two test conditions in each test block, the right-hand keypad was relocated to the mold 90° to the side of the participants’ shoulder. The chinrest was placed at 60 cm from the display to diminish any effect of the right hand being relocated over the course of the experiment and to assure that potential head-based frames of reference did not differ across participants. The room (2.25 × 2.25 × 3.50 m) was dimly lit with fluorescent light and fitted with a webcam for monitoring purposes.<fig id="Fig1"><label>Fig. 1</label>
<caption><p>Participant in the test phase condition with the <italic>right hand</italic>
on the side, the <italic>left hand</italic>
on the keypad that was occluded from vision, and the head in the chinrest</p>
</caption>
<graphic xlink:href="221_2015_4457_Fig1_HTML" id="MO1"></graphic>
</fig>
</p>
</sec>
<sec id="Sec8"><title>Task</title>
<p>Upon registering for the experiment, participants received the assignment to memorize two six-digit numbers, without telling them why. The ability to recite the numbers from memory was a prerequisite for further participation in the experiment, and one participant was rescheduled to a later time slot for not having learned the numbers. The digits in these six-digit numbers were associated with the left little finger (“1”) through the right little finger (“8”). At the start of the experiment, participants were told that only the first response of a sequence would be indicated by the location of the stimulus on the display, after which the memorized numbers were to be used as imperatives by the participant for the subsequent key presses in the sequence. Presentation of key-specific stimuli was omitted to preclude incompatible mappings between the location of a stimulus and the location of the associated response when the right hand was at the participants’ side.</p>
<p>For the little finger (“pinky”) and the ring, middle, and index fingers of the left hand (“p”, “r”, “m”, and “i”, respectively) and for the index, middle, ring fingers, and the pinky of the right hand (“I”, “M”, “R”, and “P”, respectively), the base sequences were ipIRPm (learned as 4-1-5-7-8-3) and MRmprI (6-7-3-1-2-5). The order of the sequences was counterbalanced over participants across the fingers of each hand. So, ipIRPm was counterbalanced to prMPIi, rmRIMp, and miPMRr, while MRmprI was counterbalanced to RPirmM, PIpmiR, and IMripP. Hence, the transitions between the second and third key presses in each sequence (i.e., R<sub>2</sub>
and R<sub>3</sub>
), and between R<sub>5</sub>
and R<sub>6</sub>
involved a between-hand transition for each participant. Given their design, the two sequences are indicated as the LLRRRL and RRLLLR sequences with L indicating a left-hand finger and R a right-hand finger.</p>
<p>Throughout the entire experiment, the display showed eight homogenously gray square outlines (6 × 6 mm) against a black background and with a black filling. This layout corresponds with the spatial arrangement of the assigned response keys (i.e.,/, 8, 5, 2, 3, 6, 9, and *) when the two keypads were in the adjacent frontal location. The eight squares were placed in a horizontal order with 4-mm spacing (i.e., about 0.4° at 60-cm face–display distance). The row of squares was centered in the horizontal plane and vertically aligned at about one third from the top of the display.</p>
<p>The stimulus consisted of one square lighting up by its filling becoming bright green. Participants responded by depressing the spatially compatible key, after which the square became black again. All ensuing key presses were to be deduced from the corresponding, pre-learned six-digit numbers (cf. Experiment 2 in De Kleine and Verwey <xref ref-type="bibr" rid="CR21">2009</xref>
). The completion of a six-element keying sequence is denoted a trial. Pressing a false key (i.e., failing to execute the sequence in its correct order) terminated a trial and resulted in the message “Wrong key” (in Dutch) being displayed for 500 ms. A premature first response resulted in a message saying “Too early” (in Dutch). The ensuing sequence started 1000 ms after a sequence was completed or terminated. Key release was not registered and could thus follow depressing a later key.</p>
</sec>
<sec id="Sec9"><title>Procedure</title>
<p>At the start of the experiment, the experimenter helped the participant attain a posture that would remain comfortable even when the right hand was turned 90° outward. An on-screen message instructed participants on which keys they were to place their fingers. At the end of each block, and halfway through each block, participants received feedback for 10 s displaying their average execution time and error rates. If the error rate rose above 8 %, the message “Try to respond more accurately” (in Dutch) was presented. Error rates below 3 % resulted in the message “Try to respond faster” (in Dutch) in order to prevent cautious and therefore slow key pressing.</p>
<p>The experiment consisted of nine blocks in a single session. In Block 1, both keypads were placed in the mold in front of the participant. Each practice block in this experiment was composed of an 80-trial sub-block, a 20-s break, and another 80-trial sub-block. At the end of each block, a message informed the participant the block had finished, that the participant was to wait for the experimenter, and that a 4-min break started. If necessary, the experimenter would encourage the participant to improve sequence execution by responding faster or more accurately.</p>
<p>Block 2 was the first test block. By then, all participants had learned to translate the six-digit code into motor actions. The test block was composed of two 40-trial sub-blocks separated by a break that the experimenter terminated manually. The two sub-blocks of each test block differed in the location of the right keypad, which was either in front of the participant as with the practice blocks, or placed in a mold 90° to the right (relative to the shoulder). Half of the participants started with the right keypad at the side of the body and then performed with the right keypad in front of them, while this was reversed for the other half. Next, the participants continued practice in Blocks 3 through 8 with the two keypads in the frontal position. Finally, Block 9 was the second test block, which was identical to Block 2. Across Blocks 1 through 9, participants performed 600 repetitions of each sequence with the two keypads in the frontal location, and two times 20 trials per sequence with the right-hand keypad relocated to the participants’ side.</p>
<p>Following Block 9, the participants filled out a questionnaire. It first asked participants to write down the two sequences they had been practicing (‘free recall’) in terms of the symbols on the keys they had been depressing. As support, the symbols on the actual keys were presented in the questionnaire in a spatially realistic location (i.e., /852 369*). Notice that these symbols differed from the ones the participants had been learning before the experiment (which had consisted of the numbers 1–8). Next, the participants were asked to indicate the strategy they had been using for writing the sequences down. That is, whether (a) they had remembered the order of the symbols on the keys, (b) they had remembered the order of the stimulus locations, (c) they had executed the sequences with their fingers on the table or in their mind, or (d) they had used some other strategy.</p>
</sec>
<sec id="Sec10"><title>Data analysis</title>
<p>The first two trials of each sub-block and sequences with an error were excluded from the RT analyses. Sequences were considered outliers and also removed when their total execution time was longer than the average time plus three times the standard deviation in a block. This excluded 1.8 % of the sequences. Errors were computed per block and for each sequential position. Error frequency was arcsin-transformed before being submitted to an ANOVA to stabilize the variance (p. 356 in Winer et al. <xref ref-type="bibr" rid="CR99">1991</xref>
). The times between successive keying responses are denoted: the sequence initiation interval (T<sub>1</sub>
) for the response to the stimulus and interkey intervals T<sub>2</sub>
through T<sub>6</sub>
for the five consecutive responses. Responses are denoted also by indices (R<sub>1</sub>
–R<sub>6</sub>
).</p>
</sec>
</sec>
<sec id="Sec11" sec-type="results"><title>Results</title>
<sec id="Sec12"><title>Practice blocks</title>
<p>Figure <xref rid="Fig2" ref-type="fig">2</xref>
shows the RTs obtained with both hands in the frontal location as a function of Block and Key collapsed across the two sequences. The RTs were analyzed using a 9 (Block) × 2 (Sequence: LLRRRL vs. RRLLLR) × 6 (Key) repeated-measures ANOVA. From Blocks 2 and 9 only the sub-block was included in which participants used the right hand in the normal frontal location. This ANOVA showed main effects of Block, <italic>F</italic>
(8,184) = 232.4, <italic>p</italic>
< .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .91, and Key, <italic>F</italic>
(5,115) = 67.6, <italic>p</italic>
< .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .75. These effects support the notions that participants improved with practice, and that RTs differed as a function of key position in the sequence. A significant Block × Key interaction confirmed that key presses at some sequential locations gained more from practice than others, <italic>F</italic>
(40,920) = 7.8, <italic>p</italic>
< .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .25.<fig id="Fig2"><label>Fig. 2</label>
<caption><p>Response times as a function of Block and Key position. Blocks 2 and 9 include only the sub-blocks with the <italic>right-hand</italic>
keypad in the frontal location (like in the practice blocks). Between-hand transitions occurred before R<sub>3</sub>
and R<sub>6</sub>
</p>
</caption>
<graphic xlink:href="221_2015_4457_Fig2_HTML" id="MO2"></graphic>
</fig>
</p>
<p>With respect to the effect of the between-hand transitions, Fig. <xref rid="Fig2" ref-type="fig">2</xref>
indicates that in Block 1 the second between-hand transition during T<sub>6</sub>
was not slower than the preceding responses. This implies that R<sub>6</sub>
was not treated as a separate “1-element chunk” and, hence, that a between-hand transition does not necessarily lead to a clear segmentation of a movement sequence. In Block 1, T<sub>6</sub>
was even shorter than T<sub>5</sub>
, <italic>F</italic>
(1,23) = 6.9, <italic>p</italic>
= .02, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .23, but this advantage of T<sub>6</sub>
reduced with block, <italic>F</italic>
(1,23) = 7.1, <italic>p</italic>
< .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .24, and it was no longer significant across Blocks 2–9, <italic>F</italic>
(1,23) = 0.9, <italic>p</italic>
= .34, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .04.</p>
<p>Figure <xref rid="Fig2" ref-type="fig">2</xref>
shows also that the first between-hand transition during T<sub>3</sub>
was indeed relatively slow in the earlier blocks. Planned comparisons indicated that while R<sub>3</sub>
was significantly slower than R<sub>2</sub>
and R<sub>4</sub>
together in each of the 9 blocks, Fs(1,23) > 5.7, <italic>p</italic>
s < .03, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
s > .20, in later blocks this effect can be attributed to the fast R<sub>2</sub>
and not to R<sub>4</sub>
. T<sub>3</sub>
was significantly longer than T<sub>4</sub>
only in Blocks 1 and 2, Fs(1,23) > 6.6, <italic>p</italic>
s < .02, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
s > .22, and this T<sub>3</sub>
–T<sub>4</sub>
difference was indeed significantly greater in Blocks 1–4 than in Blocks 6–9, <italic>F</italic>
(1,23) = 7.5, <italic>p</italic>
= .01, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .25. Given that the fast R<sub>2</sub>
can be attributed to response preparation on the basis of explicit sequenced knowledge (Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
), which was high (see below), these results support initial segmentation at T<sub>3</sub>
, but not at T<sub>6</sub>
, and further show that the initially slow R<sub>3</sub>
did not last with practice. Only the fast R<sub>2</sub>
, relative to R<sub>3</sub>
, persisted until Block 9, <italic>F</italic>
(1,23) = 10.4, <italic>p</italic>
= -.003, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .31.</p>
<p>Arcsin-transformed error proportions per key were subjected to the same repeated-measures ANOVA as used for the RTs. Only the first error in a sequence counted because execution of the sequence was terminated after an error. The ANOVA showed main effects of Block, <italic>F</italic>
(8,184) = 17.1, <italic>p</italic>
< .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .43, and Key, <italic>F</italic>
(5,115) = 6.4, <italic>p</italic>
< .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .22, and a Sequence × Block interaction, <italic>F</italic>
(8,184) = 2.7, <italic>p</italic>
= .008, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .11. These results indicated a relatively high error rate in Block 1 (of 3.3 % per key), and in Block 8 (2.2 % per key), while the other error proportions per key were below 2 %. The error rate was high for R<sub>3</sub>
relative to the other keys (1.9, 1.1, 2.6, 2.2, 2.2, and 1.3 %, respectively). Finally, according to the above-mentioned Sequence × Block interaction, LLRRRL had a relatively high error rate in Block 2 compared to RRLLLR (1.7 vs. 1.0 % per key), whereas error rates tended to be somewhat higher for RRLLLR in Blocks 4, 5, and 7.</p>
</sec>
<sec id="Sec13"><title>Test blocks: representing movement sequences</title>
<p>To analyze the rate at which RT changed within the test blocks after the between-hand transitions, we analyzed performance in Block 2 (i.e., after 80 or 100 practice trials per sequence), and in Block 9 (after 580 or 600 practice trials) by distinguishing four successive five-trial bins. The averages of the errorless sequences in these bins were therefore analyzed with a 4 (Bin) × 2 (Block: 2 vs. 9) × 2 (Sequence: LLRRRL vs. RRLLLR) × 2 (Location of the right hand: Front, Side) × 6 (Key) repeated-measures ANOVA (see Fig. <xref rid="Fig3" ref-type="fig">3</xref>
). In addition to the typical main effects of Block, <italic>F</italic>
(1,23) = 134.6, <italic>p</italic>
< .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= 0.85, and Key, <italic>F</italic>
(5,115) = 52.2, <italic>p</italic>
< .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .69, this ANOVA showed main effects of Bin, <italic>F</italic>
(3,69) = 41.6, <italic>p</italic>
< .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .64, and Location, <italic>F</italic>
(1,23) = 10.5, <italic>p</italic>
= .004, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .31. The sequence main effect was not significant, <italic>F</italic>
(1,23) = 1.6, <italic>p</italic>
= .21, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .07, and neither were all other interactions that included sequence and location, with the exception of the highest-order Bin × Block × Sequence × Location × Key interaction, <italic>F</italic>
(15,345) = 2.0, <italic>p</italic>
= .01, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .08). These results suggest that location had similar effects on the LLRRRL and RRLLLR sequences.<fig id="Fig3"><label>Fig. 3</label>
<caption><p>Individual RTs in Bins 1–4 of Blocks 2 and 9 pooled across the two <italic>right-hand</italic>
location conditions</p>
</caption>
<graphic xlink:href="221_2015_4457_Fig3_HTML" id="MO3"></graphic>
</fig>
</p>
<p>According to the significant Key × Location interaction, relocating the right hand slowed some sequence elements more than others, <italic>F</italic>
(5,115) = 2.6, <italic>p</italic>
= .03, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .10 (the location effect amounted to 55, 15, 52, 24, 13, and 20 ms for R<sub>1</sub>
–R<sub>6</sub>
, respectively). This is inconsistent with the applicability hypothesis and supports the adjustment hypothesis. A planned comparison confirmed that this interaction was a result of a larger location effect on responses that according to the adjustment hypothesis are preceded by an adjustment of the spatial sequence representation (i.e., R<sub>136</sub>
), than on the other responses (R<sub>245</sub>
), <italic>F</italic>
(1,23) = 7.1, <italic>p</italic>
= .01, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .24. Further support for the adjustment hypothesis comes from the significant Bin × Location interaction which shows that the slowing that resulted from relocating the right hand was reduced across successive bins (61, 29, 17, 12 ms, respectively), <italic>F</italic>
(3,69) = 3.0, <italic>p</italic>
= .04, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .12. This rapid reduction in the location effect is incongruent with the applicability hypothesis, as that would require a new representation which would probably take many more than the 20 trials per sequence available in each test block to develop. The reduction in the location effect for R<sub>136</sub>
across successive bins was not supported by a Key × Bin × Location interaction in the omnibus ANOVA, <italic>F</italic>
(15,345) = 0.99, <italic>p</italic>
= .47, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .04 [but it was significant in a Block 9 ANOVA, <italic>F</italic>
(3,69) = 2.8, <italic>p</italic>
= .05, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .11].</p>
<p>Figure <xref rid="Fig3" ref-type="fig">3</xref>
shows that the location effect had been caused by R<sub>1</sub>
and R<sub>3</sub>
, especially in the earlier bins of Block 9, and not by R<sub>6</sub>
. This was not unexpected given that the last response of a six-key sequence (just like R<sub>2</sub>
) has been found to disproportionally benefit from explicit sequence knowledge (Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
). This notion was supported by a planned comparison across both test blocks and sequences showing that the location effect was greater for R<sub>13</sub>
than for R<sub>6</sub>
, <italic>F</italic>
(1,23) = 5.6, <italic>p</italic>
= .03, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .20.</p>
<p>Given the above support for the adjustment hypothesis, we then used planned comparisons to examine the prediction of that hypothesis that adjustment should be stronger in Block 9 than in Block 2 (because execution in Block 9 involves more task-specific representations). In line with this prediction, the location effect in R<sub>13</sub>
, relative to R<sub>245</sub>
, was significant across all bins of Block 9, <italic>F</italic>
(1,23) = 11.9, <italic>p</italic>
= .002, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .34, while this was not the case with Block 2, <italic>F</italic>
(1,23) = 0.6, <italic>p</italic>
= .63, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .03. Furthermore, the location effect in R<sub>13</sub>
(relative to R<sub>245</sub>
) was significantly larger in Block 9/Bin 1 than in Block 2/Bin 1, <italic>F</italic>
(1,23) = 4.7, <italic>p</italic>
= .04, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .17. This Block difference did not reach significance across all fours bins, <italic>F</italic>
(1,23) = 2.4, <italic>p</italic>
= .13, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .09, which is reasonable given that the adjustment hypothesis suggests that the location effect reduces quite quickly within a test block. Indeed, a Location × Bin interaction in the Block 9 ANOVA reflected a reducing location effect across successive bins, <italic>F</italic>
(3,69) = 4.0, <italic>p</italic>
= .01, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .15, though the location effect was still significant across Bins 2–4, <italic>F</italic>
(1,23) = 5.3, <italic>p</italic>
= .03, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .19.</p>
<p>While the location effect was significant for R<sub>13</sub>
across both sequences, according to the adjustment hypothesis the location effect should be larger in R<sub>1</sub>
of RRLLLR than of LLRRRL, especially in Block 9/Bin 1 when representations are more task-specific than in Block 2. This prediction is supported by the earlier mentioned Bin × Block × Sequence × Location × Key interaction in the omnibus ANOVA, <italic>F</italic>
(15,345) = 2.0, <italic>p</italic>
= .01, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .08. A planned comparison to test this specific hypothesis showed that in Bin 1 of Block 9, R<sub>1</sub>
of RRLLLR was substantially slower when carried out by the relocated right hand than R<sub>1</sub>
of LLRRRL (856 vs. 581 ms, respectively), <italic>F</italic>
(1,23) = 4.6, <italic>p</italic>
= .04, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .17. Also, in Block 9/Bin 1 R<sub>1</sub>
was substantially slower with the right hand at the side than in the front, <italic>F</italic>
(1,23) = 5.1, <italic>p</italic>
= .03, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .18. Most likely because of the limited statistical power of higher-order interactions, this effect was not significantly greater in Block 9/Bin 1 than in Block 2/Bin 1, <italic>F</italic>
(1,23) = 2.8, <italic>p</italic>
= .11, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= 11.</p>
<p>Arcsin-transformed error proportions in Blocks 2 and 9 were analyzed using a 2 (Block: 2, 9) × 2 (Location) × 6 (Key) repeated-measures ANOVA. It showed main effects of Block, <italic>F</italic>
(1,23) = 6.4, <italic>p</italic>
= .02, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .22, and Key, <italic>F</italic>
(5,115) = 3.8, <italic>p</italic>
= .003, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .14, indicating a slight increase in errors after practice (1.4 vs. 2.0 % per key), and some variation across key positions (1.6, 0.7, 2.4, 2.0, 2.1, and 1.5 %, respectively). The LLRRRL sequence had a higher error rate than RRLLLR with the right hand in the frontal location (1.8 vs. 1.3 %), and a lower error rate with the right hand on the side (1.7 vs. 2.2 %), <italic>F</italic>
(1,23) = 14.1, <italic>p</italic>
= .001, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .38. The Location × Key interaction, <italic>F</italic>
(5,115) = 3.3, <italic>p</italic>
= .009, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .13, indicated that with the right hand on the side, error proportion was a little higher for R<sub>1</sub>
(frontal: 1.3 % vs. side: 1.9 %), and R<sub>4</sub>
–R<sub>6</sub>
(1.4 vs. 2.3 %), whereas it was lower for R<sub>3</sub>
(2.8 vs. 1.9 %).</p>
<p>Taken together, these analyses showed several findings in support of the adjustment hypothesis: Two of the responses that according to the adjustment hypothesis were preceded by adjustment (R<sub>13</sub>
) were slowed more by the right-hand relocation than the other responses (R<sub>245</sub>
). This slowing was greatest after more extensive practice in Bin 1 of Block 9 after which it reduced in the ensuing five-trial bins. However, R<sub>6</sub>
did not show any effects of relocating the right hand. This can be attributed to the use of explicit sequence knowledge. Finally, the location effect on R<sub>1</sub>
in the RRLLLR sequence appeared quite large, especially in Bin 1 of Block 9 (the expectation that this R<sub>1</sub>
would be relatively slow was not supported by all associated higher-order interactions which is probably due to a lack of statistical power).</p>
</sec>
<sec id="Sec14"><title>Test blocks: chunking boundaries in Blocks 2 and 9</title>
<p>We also examined the effect of the between-hand transitions in Blocks 2 and 9 in the condition in which the right hand was in the frontal location. We used the R<sub>5</sub>
–R<sub>6</sub>
difference and the R<sub>3</sub>
–R<sub>4</sub>
difference to explore whether the first response following a between-hand transition might have induced the start of a segment that eventually consolidated (we excluded R<sub>2</sub>
from the last comparison because that response was most likely sped up by explicit knowledge, Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
). It immediately stood out that R<sub>6</sub>
was never slower than R<sub>5</sub>
, not even in Block 1 (see Fig. <xref rid="Fig1" ref-type="fig">1</xref>
). In contrast, the first between-hand transition appeared to be followed by a slow R<sub>3</sub>
, that in Block 2 was 171 ms slower than R<sub>4</sub>
, <italic>F</italic>
(1,23) = 7.4, <italic>p</italic>
= .01, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .24. Detailed examination of the individual participants’ RTs per sequence showed that in Block 2 R<sub>3</sub>
was slower than R<sub>4</sub>
in only 30 of the 48 sequences (each of the 24 participants carried out 2 sequences). So, the between-hand transition certainly had no consistent effect on all participants. In Block 9, the R<sub>3</sub>
–R<sub>4</sub>
difference (of 44 ms) did not reach significance any more, <italic>F</italic>
(1,23) = 2.3, <italic>p</italic>
= .14, <italic>η</italic>
<sub arrange="stack"><italic>p</italic>
</sub>
<sup arrange="stack"><italic>2</italic>
</sup>
= .09, and R<sub>3</sub>
appeared slower than R<sub>4</sub>
in only 25 of the 48 sequences. So, like the second between-hand transition, the first between-hand transition did not seem to induce a concatenation point.</p>
</sec>
<sec id="Sec15"><title>Awareness</title>
<p>We examined the numbers of participants who correctly recorded the six elements of 0, 1, or 2 sequences. Table <xref rid="Tab1" ref-type="table">1</xref>
shows that 22 of the present 24 participants (92 %) had full awareness of two six-key sequences that were practiced. This was unexpectedly high given that the participants in five recent studies—which involved display of key-specific stimuli—showed that significantly less participants (namely 47 %) had been fully aware, χ<sup>2</sup>
(2) = 103.3, <italic>p</italic>
< .001 (these studies were reported in Ruitenberg et al. <xref ref-type="bibr" rid="CR68">2012</xref>
; Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
; Verwey and Abrahamse <xref ref-type="bibr" rid="CR87">2012</xref>
; Verwey et al. <xref ref-type="bibr" rid="CR94">2010</xref>
; Verwey and Wright <xref ref-type="bibr" rid="CR92">2014</xref>
). Due to this high awareness, we could not assess whether performance correlated with awareness (especially of R<sub>2</sub>
and R<sub>6</sub>
).<table-wrap id="Tab1"><label>Table 1</label>
<caption><p>Numbers (and percentages) of participants correctly recalling (by writing freely) 0, 1, or 2 of their two six-key sequences in the present and in the five earlier DSP studies (see text), and the numbers (and percentages) of participants who indicated to have used a particular strategy to write down their two six-key sequences in the present and in four or five earlier DSP studies (see text for details)</p>
</caption>
<table frame="hsides" rules="groups"><thead><tr><th align="left"></th>
<th align="left">Present study<break></break>
(<italic>n</italic>
= 24)</th>
<th align="left">Five recent studies<break></break>
(<italic>n</italic>
= 144)</th>
</tr>
</thead>
<tbody><tr><td align="left" colspan="3">Free recall: sequences correct</td>
</tr>
<tr><td align="left"> 0</td>
<td char="(" align="char">0 (0 %)</td>
<td char="(" align="char">38 (26 %)</td>
</tr>
<tr><td align="left"> 1</td>
<td char="(" align="char">2 (8 %)</td>
<td char="(" align="char">39 (27 %)</td>
</tr>
<tr><td align="left"> 2</td>
<td char="(" align="char">22 (92 %)</td>
<td char="(" align="char">67 (47 %)</td>
</tr>
</tbody>
</table>
<table frame="hsides" rules="groups"><thead><tr><th align="left"></th>
<th align="left">Present study<break></break>
(<italic>n</italic>
= 24)</th>
<th align="left">4 recent studies<break></break>
(<italic>n</italic>
= 93)</th>
</tr>
</thead>
<tbody><tr><td align="left" colspan="3">Awareness strategy</td>
</tr>
<tr><td align="left"> Knew spatial positions</td>
<td char="(" align="char">4 (17 %)</td>
<td char="(" align="char">21 (23 %)</td>
</tr>
<tr><td align="left"> Used finger tapping</td>
<td char="(" align="char">12 (50 %)</td>
<td char="(" align="char">63 (68 %)</td>
</tr>
<tr><td align="left"> Knew letters/symbols</td>
<td char="(" align="char">8 (33 %)</td>
<td char="(" align="char">9 (10 %)</td>
</tr>
</tbody>
</table>
</table-wrap>
</p>
<p>Half of the present 24 participants (50 %) indicated that they had reconstructed their explicit knowledge when filling out the questionnaire by executing the sequences on the table top or covertly in their heads (Table <xref rid="Tab1" ref-type="table">1</xref>
). This number of reconstructing participants was significantly less than across four previous studies (Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
; Verwey and Abrahamse <xref ref-type="bibr" rid="CR87">2012</xref>
; Verwey et al. <xref ref-type="bibr" rid="CR94">2010</xref>
; Verwey and Wright <xref ref-type="bibr" rid="CR92">2014</xref>
) where 68 % of the participants indicated to have used this strategy, χ<sup>2</sup>
(2) = 55.2, <italic>p</italic>
< .001. On the one hand, these numbers indicate that, despite the capacity of most participants to write down their sequences, still half of them had no direct access to their sequence knowledge. On the other hand, given that explicit knowledge of discrete keying sequences is highest at the start and end of a sequence due to primacy and recency effects (Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
), the high awareness in the present study show that it is quite likely that the present participants could speed up R<sub>6</sub>
using explicit knowledge.</p>
</sec>
</sec>
<sec id="Sec16" sec-type="discussion"><title>Discussion</title>
<p>In order to better understand the nature of the representations that make up the motor chunks used to execute DSP keying sequences, we explored in detail how execution of two bimanual, familiar keying sequences would be affected when the right hand is relocated to the side. Explicit sequence knowledge was assessed to see whether that kind of sequence knowledge might be used to counteract a potential hand relocation effect on, especially, R<sub>6</sub>
(Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
). We further explored whether the between-hand transitions between R<sub>2</sub>
and R<sub>3</sub>
and between R<sub>5</sub>
and R<sub>6</sub>
would induce segmentation of the sequence in early practice, and whether these would eventually consolidate into concatenation points of successive motor chunks.</p>
<sec id="Sec17"><title>Adjusting spatial representations</title>
<p>The present data support an adjustment hypothesis that assumes that practice induces highly task-specific representations that can be adjusted when one of the hands is in a new location. They are inconsistent with the applicability hypothesis that asserts that inapplicable representations are no longer used.<xref ref-type="fn" rid="Fn2">2</xref>
</p>
<p>The support for the adjustment hypothesis comes from the findings that relocating the right hand affected mostly the first response carried out by each hand (i.e., R<sub>1</sub>
and R<sub>3</sub>
in RRLLLR, and R<sub>3</sub>
in LLRRRL—but not R<sub>6</sub>
, see below), and that this slowing lasted only about 15 trials. This slowing suggests that before a hand could start executing its part of the keying sequence, the sequence representation had to be adjusted to the location of that hand. The finding that this effect reduced so quickly in the successive bins of the test blocks shows that participants quickly were able to perform this adjustment more efficiently. This efficiency may be based on performing the adjustment during execution of the preceding responses (Verwey <xref ref-type="bibr" rid="CR81">1995</xref>
, <xref ref-type="bibr" rid="CR84">2001</xref>
), but the observation that even in RRLLLR R<sub>1</sub>
rapidly became faster (in which case preparation could not be carried out during earlier responses) suggests that the adjustment itself was quickly learned. Such a rapid adjustment is in line with neurophysiological studies showing adjustment of neural representations of space in less than 50–100 ms (Derdikman and Moser <xref ref-type="bibr" rid="CR22">2010</xref>
; Georgopoulos et al. <xref ref-type="bibr" rid="CR26">1986</xref>
; Zacks <xref ref-type="bibr" rid="CR102">2008</xref>
).</p>
<p>The adjustment hypothesis is not supported by the observation that R<sub>6</sub>
did not show a hand location effect. It is possible that adjustment of R<sub>6</sub>
was easy because it involved just a single response and could entirely occur during execution of the preceding responses. Indeed, preparing one response during a preceding keying sequence seems to proceed more smoothly than when a few responses are prepared during the preceding key presses (Verwey <xref ref-type="bibr" rid="CR81">1995</xref>
, <xref ref-type="bibr" rid="CR84">2001</xref>
). Alternatively, the high awareness in the present participants of their sequences and the high saliency of the last response (one key press that was executed with another hand) may imply that the participants used explicit knowledge to speed up the last response rather than that they adjusted the sequence representation for just a single last response. This possibility is in line with the recent finding that especially the last response of a six-key DSP sequence is sped up by using explicit sequence knowledge (Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
). Preparing explicit knowledge of R<sub>6</sub>
could probably occur during execution of earlier responses because after practice, the central processor was no longer required for executing the sequence (Abrahamse et al. <xref ref-type="bibr" rid="CR2">2013</xref>
; Verwey et al. <xref ref-type="bibr" rid="CR95">2015</xref>
).</p>
<p>The current pattern of results provides some indications as to the nature of the motor chunks. The observation that sequence execution by both hands suffered equally from relocating one hand suggests that after about 600 trials the sequence representation relied primarily on a cross-hand trunk- or head-based reference frame that was adjusted at each between-hand transition. While neurophysiological research provided evidence for the existence of hand-based reference frames (Zacks <xref ref-type="bibr" rid="CR102">2008</xref>
), the present finding that relocating one hand slowed both hands suggests that sequence execution did not rely much on such hand-specific, egocentric representations. Basically, allocentric representations may have played a role as well, but these are not believed to play an important role at advanced levels of movement execution (Willingham <xref ref-type="bibr" rid="CR98">1998</xref>
). Earlier findings that execution rate is slowed when a sequence is carried out by other effectors, should probably be attributed to a spatial representation that is also effector-specific (Andresen and Marsolek <xref ref-type="bibr" rid="CR8">2012</xref>
; Park and Shea <xref ref-type="bibr" rid="CR59">2005</xref>
; Verwey and Clegg <xref ref-type="bibr" rid="CR88">2005</xref>
; Verwey and Wright <xref ref-type="bibr" rid="CR91">2004</xref>
), rather than to a muscle-oriented representation (Hikosaka et al. <xref ref-type="bibr" rid="CR30">1999</xref>
; Keele <xref ref-type="bibr" rid="CR34">1968</xref>
; Shea et al. <xref ref-type="bibr" rid="CR75">2011</xref>
; Verwey et al. <xref ref-type="bibr" rid="CR95">2015</xref>
). This dominant role of an effector-specific spatial representation is in line with findings with DSP sequences that execution rate reduced more when fingers of the other hand were used (Verwey and Wright <xref ref-type="bibr" rid="CR91">2004</xref>
) than adjacent fingers of the same hand (Verwey et al. <xref ref-type="bibr" rid="CR93">2009</xref>
). Participants in the latter study using adjacent fingers seem to have been able to make better use of the spatial hand-specific representations than in the former study where the other hand was being used. It should be noted, however, that the present results do not necessarily reject the possibility that sequence coding did include a component that was muscle specific or in a hand-based reference frame. For example, early in Block 9, participants may have relied on such a hand-based representation. Still, the dominant representations in Block 9 seem to have been one coded in a cross-hand trunk- or head-based spatial reference frame.</p>
<p>The finding that R<sub>1</sub>
and R<sub>3</sub>
in RRLLLR were both slowed indicates that a sequence representation was activated in memory, and it was then adjusted before executing R<sub>1</sub>
and then adjusted again before executing R<sub>3</sub>
. In terms of motor buffer models, like the dual processor model (Verwey <xref ref-type="bibr" rid="CR84">2001</xref>
), this shows that motor chunk representations that have already been loaded into the motor buffer can still be adjusted to different spatial conditions. Apparently, once loaded the motor buffer remains open to cognitive manipulations.</p>
</sec>
<sec id="Sec18"><title>No consolidation of between-hand transitions</title>
<p>We further examined whether segmentation with limited practice may be determined by salient between-hand transitions and whether this would consolidate into motor chunks with practice. It was immediately obvious that R<sub>6</sub>
was never faster than R<sub>5</sub>
. And while across all participants R<sub>3</sub>
appeared to be significantly slower than R<sub>4</sub>
in Block 2, this pattern occurred in only about two-thirds of the 48 averaged sequences per participant and block (2 sequences per participant in each block). In Block 9 the R<sub>3</sub>
–R<sub>4</sub>
difference did not reach statistical significance at all. These results reject the hypothesis that in discrete keying sequences a between-hand transition is an important determinant of segmentation and chunking. This endorses the idea that motor chunks—at this level of practice—do not include hand-based representations, but include cross-hand representations.</p>
</sec>
</sec>
<sec id="Sec19" sec-type="conclusion"><title>Conclusions</title>
<p>The present study indicates that after 600 practice trials per sequence, motor chunks in a DSP task rely heavily on a cross-hand representation that codes individual key presses in a trunk- or head-based spatial reference frame. Recent indications that explicit knowledge is especially important for the last response in a six-key sequence (Verwey <xref ref-type="bibr" rid="CR86">2015</xref>
) suggests that the lack of a hand location effect on R<sub>6</sub>
was caused by the use of explicit knowledge. After these 600 practice trials, it took only about 15 trials to fully adjust this representation to a novel location of the right hand. This spatial sequence representation seems to be implicit in the sense that, despite the high scores on an awareness test, half of the participants indicated that to write down the sequence elements they had to reconstruct their sequences by mentally or physically “executing” them. No indication was found for a clear contribution of a muscle-based (motor) representation or a hand-based spatial representation as that should have made execution rate of all sequence elements insensitive to the changed right-hand location. Indications for effector-specific learning—previously taken as evidence for motor learning—can perhaps be explained better by an adjustment of the timing to the biomechanical properties of the effectors used (Park and Shea <xref ref-type="bibr" rid="CR58">2003</xref>
; Shea and Kovacs <xref ref-type="bibr" rid="CR74">2013</xref>
). Nevertheless, a role of hand-based representations cannot be excluded yet. Such a representation may have been responsible for executing the sequences in the trials immediately after the hand had been relocated. Finally, the present data indicate that a between-hand transition may perhaps influence how some participants strategically segment their sequences in early practice, but there are no indications that these transitions determine the sequential positions at which successive motor chunks are eventually concatenated.</p>
</sec>
</body>
<back><fn-group><fn id="Fn1"><label>1</label>
<p>Segmentation involves the perceivable grouping of elements that probably reflects some cognitive strategy, whereas motor chunking explicitly suggests the use of integrated sequence representations (Verwey and Eikelboom <xref ref-type="bibr" rid="CR90">2003</xref>
).</p>
</fn>
<fn id="Fn2"><label>2</label>
<p>Because the adjustment hypothesis predicts effects especially after substantial practice, we performed also an ANOVA on just Block 2 results which is not reported here. In that block, the location effect did not reach significance, neither across all responses nor for some responses alone. This is consistent with the notion that performance in Block 2 was still largely based on sequence representations that are not hand location-specific (like the learned 6-digit numbers). In other words, the lack of significant location effects in Block 2 supports the assumption of the applicability hypothesis that the location effect in Block 9 is based on slower developing representations.</p>
</fn>
</fn-group>
<ack><p>This experiment was carried out by Eduard C. Groen in fulfillment of his bachelor’s thesis requirements. We thank Elian de Kleine and Elger L. Abrahamse for their support in all phases of the study.</p>
</ack>
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