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Coordination and Variability in The Elite Female Tennis Serve
Coordination and Variability in The Elite Female Tennis Serve
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To cite this article: David Whiteside, Bruce Clifford Elliott, Brendan Lay & Machar Reid (2014): Coordination and variability in
the elite female tennis serve, Journal of Sports Sciences, DOI: 10.1080/02640414.2014.962569
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Journal of Sports Sciences, 2014
http://dx.doi.org/10.1080/02640414.2014.962569
DAVID WHITESIDE1, BRUCE CLIFFORD ELLIOTT1, BRENDAN LAY1 & MACHAR REID2
1
School of Sport Science, Exercise and Health, University of Western Australia, Crawley, Australia and 2Sports Science and
Medicine Unit, Tennis Australia, Melbourne, Australia
Abstract
Enhancing the understanding of coordination and variability in the tennis serve may be of interest to coaches as they work
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with players to improve performance. The current study examined coordinated joint rotations and variability in the lower
limbs, trunk, serving arm and ball location in the elite female tennis serve. Pre-pubescent, pubescent and adult players
performed maximal effort flat serves while a 22-camera 500 Hz motion analysis system captured three-dimensional body
kinematics. Coordinated joint rotations in the lower limbs and trunk appeared most consistent at the time players left the
ground, suggesting that they coordinate the proximal elements of the kinematic chain to ensure that they leave the ground at
a consistent time, in a consistent posture. Variability in the two degrees of freedom at the elbow became significantly greater
closer to impact in adults, possibly illustrating the mechanical adjustments (compensation) these players employed to
manage the changing impact location from serve to serve. Despite the variable ball toss, the temporal composition of the
serve was highly consistent and supports previous assertions that players use the location of the ball to regulate their
movement. Future work should consider these associations in other populations, while coaches may use the current findings
to improve female serve performance.
Correspondence: David Whiteside, School of Sport Science, Exercise & Health, University of Western Australia, 35 Stirling Highway, Crawley, Perth 6009,
Australia. E-mail: davidwhiteside@gmail.com
Documenting the variability of movement patterns 1990), pistol shooting (Scholz, Schoner, & Latash,
within the serve may uncover how tennis players 2000) and dart throwing (Smeets et al., 2002). Since
coordinate joint rotations to produce accurate, high mechanical compensation is an inherent biomechani-
speed serves. Despite a long history of research cal response to the demands presented when enacting
describing movement variability and its functional a particular movement task, it does not follow a con-
relevance to human movement (Hatze, 1986; sistent pattern. Therefore, variations in joint rotations
Winter, 1984), movement variability in sporting (or other mechanics) are no longer considered to be
motions was often considered noise (Bartlett et al., indicative of movement system ineptitude. Rather,
2007). While this viewpoint has been tempered by movement variability is now considered critical to
contemporary movement research, consistency in the stabilisation of the performance parameters that
some parameters related to performance is still con- directly govern the outcome of the task (e.g. launch
sidered critical to success. parameters in the serve). In other words, variability in
In hitting and projectile tasks, the launch para- the movement system is not detrimental so long as the
meters critical to success relate to the trajectory and critical end point parameters remain stable. This
orientation of the end-effector (i.e. the racquet, bat, notion is reflected in recent tennis research, where
club, in hitting tasks, or the hand in throwing tasks), Whiteside et al. (2013b) showed that increased varia-
as its terminal location, orientation and velocity will bility in coordinated elbow and wrist joint rotations
ultimately determine the outcome of the task. did not reduce serve accuracy. Given the whole-body
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Indeed, a single study on the tennis serve has nature of the serve, other mechanics may also con-
reported that consistency in speed and location of tribute to the compensatory process but are yet to be
the serving hand around impact is positively related characterised.
to serve speed and accuracy (Antúnez, Hernández, Movement variability in sporting actions is not
García, Vaíllo, & Arroyo, 2012). Other launch para- restricted to the magnitudes of discrete joint rota-
meters that directly govern the outcome of the serve tions. Research in other striking skills has highlighted
include the impact height, ball projection angle and the importance of consistent temporal patterns (i.e.
racquet velocity, the combination of which are the times at which specific movements occur) in
thought to determine serve outcome (Whiteside, interceptive (batting) skills in cricket (Renshaw,
Elliott, Lay, & Reid, 2013b). Though these launch Oldham, Davids, & Golds, 2007) and baseball
parameters are known to be important, the coordi- (Katsumata, 2007), as well as the volleyball serve
nated joint rotations that regulate their consistency (Davids, Kingsbury, Bennett, & Handford, 2001).
are not well understood. It has been suggested that these athletes utilise infor-
Contemporary motor control research in sport mation from the incoming ball (i.e. its location) to
describes a particular form of coordinated joint rota- regulate the initiation of key propulsive movements,
tion, referred to as mechanical compensation. In hence ensuring that they intercept it at the appropri-
human movement, this mechanism helps to regulate ate moment. Similar strategies have been found in
the performance parameters that ultimately deter- the tennis serve, where players regulate their move-
mine the outcome of the task (Dupuy, Mottet, & ments such that their arrival in the trophy position
Ripoll, 2000; Kudo, Tsutsui, Ishikura, Ito, & coincides with ball zenith (Reid, Whiteside, &
Yamamoto, 2000; Smeets, Frens, & Brenner, 2002). Elliott, 2010; Whiteside, Elliott, Lay, & Reid,
More explicitly, inadvertent variations in a given 2013a). Likewise, the timing of peak forward racquet
execution parameter (e.g. a joint angle) are counter- velocity is considered critical to accuracy in the first
acted by the actions of other execution parameters serve (Antúnez et al., 2012). Ultimately, coordinated
(Davids, Glazier, Araujo, & Bartlett, 2003). In this joint rotations and/or temporal consistency may be
way, errors that are introduced into the movement thought of as techniques that players exploit to sim-
system during performance can be managed, thus plify complex sporting movements. With this in
preventing any negative influence on the task out- mind, it is expected that tennis players simplify
come that they would otherwise produce. those aspects of the serve that are most important
Mechanical compensation has been highlighted in to performance. At present, the particular methods
numerous projectile and striking sports including employed to do so are somewhat unclear as this
golf drives (Horan, Evans, & Kavanagh, 2011), free topic is yet to be comprehensively examined in the
throw shooting in basketball (Button, MacLeod, tennis serve.
Sanders, & Coleman, 2003; Mullineaux & Uhl, It has been suggested that, in learning movement
2010), underarm throwing (Dupuy et al., 2000; skills, inexperienced performers initially reduce the
Kudo et al., 2000), overarm throwing (Wagner, skill complexity by restraining degrees of freedom
Pfusterschmied, Klous, Von Duvillard, & Müller, (Anderson & Sidaway, 1994; Stergiou & Decker,
2012), table tennis forehands (Bootsma & Van 2011). These degrees of freedom are then gradually
Wieringen, 1990), tennis forehands (Knudson, released as players become more familiar with the
Coordination and variability in the tennis serve 3
Table I. Mean (± standard deviation) age, physical and menarchial characteristics of participants.
Group N Age (years) Height (cm) Mass (kg) Experienced menarche Time since menarche
task and explore alternative solutions to the move- and were arranged into pre-pubescent, pubescent
ment problem (Gentile, 2000; Newell, Deutsch, and adult groups based on their age and menarchial
Sosnoff, & Mayer-Kress, 2006). In this sense, chil- status (Table I). At the time of testing, players in the
dren are often considered novices owing to their pre-pubescent and pubescent groups held a top 8
motor inexperience (Guarrera-Bowlby & Gentile, national ranking for their respective age groups,
2004). Indeed, the popular “ten year (10,000 h) while the adult players possessed a professional
rule” (Ericsson, Krampe, & Tesch-Römer, 1993) (Women’s Tennis Association: WTA) ranking
virtually precludes any attempt to categorise children higher than 325. This cohort was the same as that
as expert performers. This position is offered partial used in a previous study (Whiteside et al., 2013a).
support by Newell’s constraints model (Newell,
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player’s fastest serves landing in the target area were hand. Ball zenith represented the peak vertical dis-
selected for analysis. placement of the ball during its toss. The subsequent
nadir of vertical racquet displacement was the rac-
quet low point, which is usually coincident with a
Data processing player leaving the ground (Bonnefoy, Slawinski,
Gaps in the raw marker trajectories were interpolated Leveque, Riquet, & Miller, 2009). Impact was
using a cubic spline within the VICON Nexus soft- defined as the frame (i.e. 0.002 s) prior to racquet-
ware. A second-order polynomial extrapolation spe- ball contact. The duration of the serve was consid-
cific to tennis limited the distortion of kinematic data ered as the time period between ball release and
around impact (Knudson & Bahamonde, 2001; impact. Leg drive was defined as the period from
Reid, Campbell, & Elliott, 2012). Data were subse- ball zenith to racquet low point, while racquet low
quently filtered using a Woltring filter (Woltring, point to impact was considered the forwardswing
1986) with the optimal mean squared error of phase of the serve.
2 mm determined by a residual analysis, and then
modelled using the University of Western Australia’s
full body (Besier et al., 2003; Lloyd et al., 2000), Variables of interest
racquet and ball (Whiteside et al., 2013) models. To gauge inter-limb coordination during leg drive,
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Joint rotations were expressed using the Euler ZXY the relative bilateral flexion-extension motion of the
sequence. Trunk rotations were expressed relative to ankles was compared, as was the relative bilateral
a virtual anatomical reference frame (x pointing for- flexion-extension motion of the knees. The relative
ward towards the net, y pointing up and z pointing transverse (twist) and frontal plane (shoulder-over-
right) originating at the global origin. To maintain shoulder) trunk rotations prior to impact indicated
consistency in the statistical analyses, kinematics for how players manipulated the trunk during this time,
the left-handed players were inverted where appro- while relative extension and pronation denoted the
priate such that all players could be considered same for the elbow in the serving arm. The location
together as right-hand dominant (Campbell, of the ball during the toss was expressed relative to
Straker, O’Sullivan, Elliott, & Reid, 2013; the front toe (Chow et al., 2003; Reid et al., 2011),
Whiteside et al., 2013b). and its spatial variability measured at both ball zenith
and impact. Finally, the timing of both ball zenith
and racquet low point (expressed as a percentage of
Relevant events of the service action
the serve), and also duration of forwardswing pro-
Figure 1 denotes how the service action was deemed vided an insight into the temporal pattern of the
to begin at the instant the ball was released from the service action.
dence value ±5% of the relevant event represented test according to the correction method proposed by
the variability at that time point. Holm (1979). The p-value was not sufficient to
The 3D (xσ , yσ and zσ ) standard deviations of ball reject the null hypothesis in the eleventh test, indi-
displacement at ball zenith and impact were calcu- cating that all significance in this study was reported
lated for each player across their five trials. The using a p-value of 0.0125. The temporal variability of
mean and standard deviations of these standard ball zenith, racquet low point and forwardswing
deviations provided a gauge of ball toss variability duration were interpreted descriptively.
for each group (Davids et al., 2001; Reid et al.,
2010). Further, each standard deviation was doubled
(effectively creating error bar representing one stan- Results
dard deviation either side of the mean, in each
dimension) and then multiplied (2xσ 2yσ 2zσ ) Ankle mechanics
to yield the “variability volume”: a singular quantity The representative traces in Figure 2 represent how
of the ball’s 3D spatial variability for each player, all groups utilised simultaneous plantar flexion at
across their five serves. both ankles and simultaneous extension in both
Figure 2. Mean coefficients of correspondence and representative angle–angle plots for the ankles and knees.
Note: *Significant difference between ball zenith and racquet low point in all groups.
6 D. Whiteside et al.
Trunk mechanics
The variability of concurrent frontal and transverse
plane trunk rotations revealed a significant main
effect for group (F2,28 = 10.530; P < .001), wherein
relative trunk rotations were significantly more con-
Figure 3. Mean ranges of flexion-extension motion at the ankles sistent in the pubescent (MD: 0.08; CI: 0.03–0.13;
and knees during leg drive. P = .001) and adult (MD: 0.08; CI: 0.02–0.13;
P = .005) groups compared with the pre-pubescent
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Figure 4. Mean coefficients of correspondence and representative angle–angle plots for the trunk and elbow.
Note: *Significant difference between the time points in all groups. † Significant difference between racquet low point and impact in the
adult group.
Figure 5. Mean ranges of motion at the trunk and elbow between Discussion
ball zenith and impact.
Coaching texts often stress the importance of coordi-
Note: *Significant difference between groups. nation and rhythm in the serve (Bollettieri, 2001;
Elliott & Saviano, 2001; Yandell, 1999). Developing
the understanding of coordinated joint rotations and
P < .001) greater in the adult group compared with movement variability may help coaches to conceptua-
the pubescent (MD: 17.33°; CI: 8.12–26.55°; lise specific aspects of coordination and translate them
P < .001) and pre-pubescent (MD: 17.78°; CI: to practice. The present study extends the understand-
4.14–23.18°; P = .002) groups (Figure 5). ing of the service action in these respects, across three
developmentally different groups of elite female
players. For example, prepubescent players were
Spatial variability of the ball toss
observed to extend their ankles and knees through a
The variability volumes were not significantly smaller range than pubescent and adult players during
affected by group (F2,28 = .371; P = .694). leg drive. More universally, the variability of lower limb
However, a main effect for time (F1,28 = 23.065; and trunk postures, in all players, decreased between
P < .001) revealed that the spatial location of the ball zenith and the moment that they left the ground.
ball was significantly more variable at impact Thereafter, significant increases in the variability of
8 D. Whiteside et al.
Table II. Two-way mixed ANOVA results for ball variability volumes at ball zenith and impact.
Ball zenith location x 7 ± 3 6 ± 2 7 ± 3 for why a reduced leg drive magnitude has been
(cm) y 6 ± 3 6 ± 3 8 ± 2 reported in prepubescent females (Whiteside et al.,
z 5 ± 2 6 ± 3 6 ± 2
2013a). Given that lower limb motions contribute
Impact location x 11 ± 4 9 ± 3 10 ± 5
(cm) y 12 ± 5 10 ± 5 12 ± 5 significantly to the force required in the tennis serve
z 5 ± 1 5 ± 3 3 ± 1 (Kibler, 1995), junior coaches should be mindful of
Ball zenith timing 2.4 ± 2.6 1.4 ± 0.8 1.4 ± 0.6 this potential limitation in the immature service
(% of toss) action. More explicitly, it has been hypothesised that
Racquet low-point 1.3 ± 0.9 0.9 ± 0.7 0.5 ± 0.4
leg drive is a precursor to trunk rotations
timing (% of
toss) (Bahamonde, 2000), pre-stretching of the shoulder
Forwardswing .04 ± .03 .02 ± .02 .03 ± .01 (Bahamonde, 1997) and racquet speed (Reid et al.,
duration (s) 2008), all of which would then be limited in the pre-
pubescent serve.
Note: x = left–right; y = forward–backward; z = up–down.
In all three groups, variability in bilateral exten-
sion at the ankles and knees decreased significantly
trunk and/or elbow joint rotations appeared to be a between the start (ball zenith) and end (racquet
functional response to the varying impact location, low point) of leg drive. With racquet low point
thereby allowing these players to achieve a suitable representing the time at which players generally
racquet-ball impact as the ball location changed from leave the ground (Bonnefoy et al., 2009), it
serve to serve. In other words, the timing at and pos- appears that players of all ages act to sequentially
ture in which these players left the ground was rela- reduce variability in lower limb motion up to this
tively consistent; however, while airborne, their trunk time. In doing so, players may find it easier to
and elbow mechanics generally became more variable. produce a more consistent vertical propulsion. At
Practically, these findings encourage coaches to incor- both ball zenith and racquet low point, the pub-
porate deliberate (though not extreme) perturbations escent group exhibited significantly more variable
of the service action to cultivate appropriate coordina- relative ankle motions than the pre-pubescent and
tive joint rotations and perception-action coupling in adult groups and may represent an intermediate
the tennis serve. stage of motor development. To this point, their
disparate ranges of motion at the ankle denote how
the pre-pubescent (less RoM) and adult (more
RoM) groups used different motor patterns at the
Lower limb mechanics
ankles, each of which was highly consistent in its
During leg drive, the angle–angle traces illustrate own right. In the pre-pubescent group, reduced
simultaneous plantar-flexion at both ankles and ankle involvement (i.e. “freezing”) may be indica-
simultaneous extension at both knees. This is not tive of a deliberate attempt to reduce the complex-
surprising and demonstrates how elite players are ity of the movement, allowing these players to
able to coordinate bilateral extension at the lower develop a more repeatable action. In contrast,
limb joints to propel their bodies off the ground additional years of practice and greater lower
(Bahamonde, 2000; Girard, Micallef, & Millet, limb strength may have afforded the adult players
2005; Reid et al., 2008). It should be noted, however, more masterful coordination of the ankles through
Coordination and variability in the tennis serve 9
rotations were evident from the angle–angle traces this degree of freedom thereafter. Restraining prona-
in all groups, though their respective magnitudes tion effectively reduces the elbow joint to a single
differed. Independent of group, twist and degree of freedom and offers an explanation for the
shoulder-over-shoulder rotations initially occurred lower coefficient of correspondence at the elbow in
together, before the latter motion was restrained in junior players. This mechanism may be an attempt
the two younger groups as they approached to reduce the complexity of the movement and, in
impact. With leg drive generating momentum turn, the margin for error at impact. A potential
that may be transferred to the trunk (Bahamonde, drawback of this approach is that the face of the
2000), the smaller range of frontal plane trunk racquet is more “open” during the forwardswing,
rotation in the pre-pubescent group is not unex- likely providing greater aerodynamic resistance com-
pected in light of the lower limb results. These pared with adult players who cut through the air with
findings support previous work where the magni- the edge of their “closed” racquets. Further, restrict-
tude of shoulder-over-shoulder rotation has been ing this degree of freedom logically limits the com-
shown to be significantly (5–9%) smaller in junior pensatory potential of the system and, in turn, its
players compared with their adult counterparts adaptability. It follows that this would leave their
(Whiteside et al., 2013a). movement systems more susceptible to perturba-
Despite being significantly more variable in the tions. However, it is also possible that young players
pre-pubescent group, the trunk orientation at rac- rely on other degrees of freedom (e.g. at the shoulder
quet low point was the most repeatable mechan- and/or wrist) for compensatory purposes. Combined
ical feature of each group’s service action. That with relatively lower muscle strength, this fact may
this trunk posture was relatively variable at the be relevant to upper extremity pathologies and pro-
commencement of leg drive (ball zenith), but vides an avenue for future work.
then extremely repeatable at the end of leg drive The diverging angle–angle curves at impact clearly
(racquet low point), points to a functional impor- show that variable and abrupt, low-magnitude pro-
tance of trunk postures at the time these players nation or supination movements were common
left the ground. Similar phenomena have been immediately prior to impacting the ball.
described for elite golfers, where the attainment Interestingly, previous work has noted similar varia-
of consistent postures at certain critical time tions in pronation-supination mechanics immedi-
points of the golf swing are considered features ately prior to impact (Elliott et al., 1995; Sprigings,
of skilled performance (Bradshaw et al., 2009). Marshall, Elliott, & Jennings, 1994; Tanabe & Ito,
Therefore, the significant reduction in variability 2007; Van Gheluwe, De Ruysscher, & Craenhals,
towards a highly repeatable trunk posture at rac- 1987). Tanabe and Ito (2007) proposed that, in
quet low point may be indicative of an equivalent faster servers, the emergence of pronation-supina-
posture in the tennis serve. Subsequent to racquet tion was dependent on shoulder mechanics and
low point, relative trunk motion became signifi- helps to orient the racquet for impact. In other
cantly more variable in all players and likely words, joint motions were not independent of one
represents postural adjustments required to man- another and emerged synergistically, according to
oeuvre the body correctly for impact. the unique needs of each serve. The variable
10 D. Whiteside et al.
magnitudes and directions of the elbow joint rota- 0.5% ± 0.4%). Therefore, not only are lower limb
tions around impact in this study are consistent with and trunk postures repeatable at racquet low point,
compensatory function that may help to ensure a but the event itself occurs at a highly repeatable time
suitable racquet-ball impact. These compensatory point of the service action. This temporal stability is
motions seem to intensify after the onset of puberty, consistent with other striking actions, where the tem-
coinciding with an increased involvement of prona- poral initiation of propulsive movements has been
tion in the serve. The location of the ball at impact shown to be highly repeatable in baseball
may help to further explain the mechanical compen- (Katsumata, 2007) and cricket batting (Renshaw
sation in question. et al., 2007) as well as volleyball serving (Davids
et al., 2001). Indeed, it has already been suggested
that tennis players use the location of the ball to reg-
Spatial variability of the ball toss
ulate their preparatory movements in the serve such
After the ball leaves the hand, the server has no con- that their arrival in the trophy position coincides with
trol over its trajectory and must move appropriately to ball zenith (Reid et al., 2010; Whiteside et al., 2013a).
intercept it. For this reason, body and racquet move- The players in this study may have used the same
ments are heavily dependent on the ball toss. It could method to ensure that racquet low point occurs at a
be argued that a repeatable ball toss would mitigate its relatively consistent juncture of the serve. Considering
influence on biomechanics; however, the values in that racquet low point represents the beginning of for-
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Table III suggest that perhaps the ball toss is less wardswing, regulating the occurrence of this event also
consistent than many coaches appreciate. From the stabilises the duration of forwardswing. This strategy
variability volume, it can be conservatively assumed effectively prevents the movement system from collap-
that the ball was placed anywhere within a ≈1500– sing in the presence of a variable ball toss since action
2500 cm3 area of space at ball zenith and, by impact, and perception are coupled. For example, if the ball
this volume had increased to ≈3000–4400 cm3. This toss is slightly higher than intended, the player com-
endorses the growing body of scientific work that has mensurately protracts the initial phase of their service
demonstrated how elite players do not use a highly action, thus delaying the initiation of forwardswing.
consistent ball toss (Reid et al., 2010, 2011; Having ensured that they will arrive at impact at an
Whiteside, Giblin, & Reid, 2014). More importantly, appropriate time, the player’s final dilemma is achiev-
a changing impact location from serve to serve man- ing an appropriate racquet orientation at impact. The
dates movement variability in the service action. solution appears to lie in the subtle mechanical adjust-
Given that the ball location (a) varies between serves ments (i.e. mechanical compensation) in the distal
and (b) ultimately shapes the mechanics of the service joints that help to manoeuvre the racquet to intercept
action, it appears more important for players to learn the ball.
how to perceive and respond to the varying ball loca- Future work may wish to explore smaller targets to
tion rather than develop a perfectly consistent action determine whether the size of the target contributed
(which may be impossible anyhow; Whiteside to any of the variability recorded in this study.
et al., 2013b, 2014). While the absolute ball location Studying their disposition in unsuccessful serves
was more variable at impact – akin to previous work in could also reveal how the mechanics examined in
tennis (Reid et al., 2010, 2011) – its vertical location this study relate to accuracy. Similarly, exploring
was most consistent at this time. This seemingly con- other joint mechanics and/or couplings would help
firms that impact height is a critical launch parameter to develop a more comprehensive understanding of
that is highly consistent in successful serves (Elliott, coordination in the serve. Instructional methods
Marsh, & Blanksby, 1986; Reid, Elliott, & Alderson, aimed at developing coordinated joint rotations
2007; Whiteside et al., 2013b) and which coaches and/or perception-action coupling in the serve
should aim to refine. could also be appraised to improve coaching techni-
ques. Further, perception-action couplings in the
serve could be evaluated more directly by quantify-
Temporal variability of the ball zenith and racquet low-
ing gaze behaviour during the ball toss.
point events
The occurrence of ball zenith, though significantly ear-
Conclusion
lier in the pre-pubescent group, was highly consistent
within the groups as evidenced by the respective stan- The elite female tennis players in this study appeared
dard deviations (pre-pubescent group: 2.4% ± 2.6% of to reduce movement variability in the lower limbs
serve; pubescent: 1.4% ± 0.8%; adult: 1.4% ± 0.6%). and trunk between the trophy position (i.e. ball
The standard deviations of racquet low-point timing zenith) and the time that they leave the ground (i.e.
were more consistent still (pre-pubescent: racquet low point). They also left the ground at a
1.3% ± 0.9%; pubescent: 0.9% ± 0.7%; adult: highly consistent time point of the service action,
Coordination and variability in the tennis serve 11
which acted to stabilise the duration of forward- Bradshaw, E., Keogh, J., Hume, P., Maulder, P., Nortje, J., &
swing. Given that this temporal consistency persisted Marnewick, M. (2009). The effect of biological movement
variability on the performance of the golf swing in high- and
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seemingly used information from the ball to deter- Sport, 80(2), 185–196.
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body movements. After becoming airborne, subtle Examining movement variability in the basketball free-throw
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