Biomechanics and Medicine in Swimming XI
Biomechanics and Medicine in Swimming XI
Biomechanics and Medicine in Swimming XI
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
<strong>Biomechanics</strong><strong>and</strong>medic<strong>in</strong>e<strong>in</strong>swimm<strong>in</strong>gXi<br />
<strong>and</strong> the end of the arm stroke phases <strong>in</strong> front crawl (entry+catch, pull,<br />
push, recovery), Chollet et al. (2000) established an <strong>in</strong>dex of coord<strong>in</strong>ation<br />
(IdC) that quantifies the time lag between the propulsion of one<br />
arm <strong>and</strong> that of the second arm. The IdC has been adapted for the four<br />
strokes (backstroke, Chollet et al., 2008; butterfly, Chollet et al., 2006;<br />
breaststroke, Chollet et al., 2004; for a review, Chollet & Seifert, 2010,<br />
Seifert & Chollet, 2008) <strong>in</strong> order to assess the time gaps quantify<strong>in</strong>g the<br />
upper limb coord<strong>in</strong>ation <strong>in</strong> the alternat<strong>in</strong>g strokes <strong>and</strong> the upper-lower<br />
limb coord<strong>in</strong>ation <strong>in</strong> the simultaneous strokes. Therefore, when IdC =<br />
0%, the mode is opposition; when IdC < 0%, the mode is catch-up; <strong>and</strong><br />
when IdC > 0%, the mode is superposition. From a functional po<strong>in</strong>t of<br />
view, it is nevertheless reasonable to consider the opposition mode as<br />
-1% < IdC < 1%. It should also be noted that these <strong>in</strong>dicators rema<strong>in</strong><br />
<strong>in</strong>dices of coord<strong>in</strong>ation <strong>and</strong> not propulsion. Coord<strong>in</strong>ation can be studied<br />
from an ‘egocentric’ po<strong>in</strong>t of view (degrees of freedom, i.e. limb movement<br />
possibilities like flexion <strong>and</strong> extension, pronation <strong>and</strong> sup<strong>in</strong>ation,<br />
rotation, etc.) rather than from an ‘allocentric’ po<strong>in</strong>t of view (propulsion<br />
phases <strong>and</strong> concepts). Seifert et al. (2010a) therefore recently assessed<br />
upper-lower coord<strong>in</strong>ation <strong>in</strong> breaststroke from the angle <strong>and</strong> angular<br />
velocity of the elbow <strong>and</strong> knee to determ<strong>in</strong>e their coupl<strong>in</strong>g by the calculation<br />
of the cont<strong>in</strong>uous relative phase.<br />
Two swimmers can achieve the same performance (swimm<strong>in</strong>g<br />
speed) us<strong>in</strong>g different modes of <strong>in</strong>ter-limb coord<strong>in</strong>ation. Thus, a second<br />
question arises: Is there a relationship between coord<strong>in</strong>ation <strong>and</strong><br />
performance? In other words, is there an ideal <strong>in</strong>ter-limb coord<strong>in</strong>ation<br />
mode? Should the coach advise the swimmer to favour superposition<br />
coord<strong>in</strong>ation rather than opposition? Is the catch-up or glide mode a<br />
technical mistake? Should the beg<strong>in</strong>ner imitate the expert swimmer?<br />
Or is it reasonable to allow a temporary ‘non-expert’ coord<strong>in</strong>ation mode<br />
at the beg<strong>in</strong>n<strong>in</strong>g of the learn<strong>in</strong>g <strong>and</strong> tra<strong>in</strong><strong>in</strong>g process? The aim of this<br />
paper is to show that coord<strong>in</strong>ation emerges pr<strong>in</strong>cipally from <strong>in</strong>teract<strong>in</strong>g<br />
constra<strong>in</strong>ts (Newell, 1986): environmental (aquatic resistances <strong>and</strong><br />
speed as resistance equal to speed squared), task (imposed by the operator,<br />
e.g. swimm<strong>in</strong>g at maximal <strong>in</strong>tensity, swimm<strong>in</strong>g <strong>in</strong> fatigue condition)<br />
<strong>and</strong> organismic (correspond<strong>in</strong>g to the swimmer’s characteristics,<br />
i.e. anthropometry, morphology, strength, etc.). From this perspective,<br />
the swimmer’s <strong>in</strong>ter-limb coord<strong>in</strong>ation is a consequence of <strong>in</strong>teract<strong>in</strong>g<br />
constra<strong>in</strong>ts <strong>and</strong> not a cause (for a review, see Davids et al., 2008). Thus,<br />
coaches should (i) take the organismic constra<strong>in</strong>ts <strong>in</strong>to account, (ii) f<strong>in</strong>d<br />
means to m<strong>in</strong>imize the environmental constra<strong>in</strong>ts, <strong>and</strong> (iii) manipulate<br />
the task constra<strong>in</strong>ts to destabilize <strong>in</strong>adequate coord<strong>in</strong>ation <strong>in</strong> order to<br />
br<strong>in</strong>g about a coord<strong>in</strong>ation mode not expected from the beg<strong>in</strong>ner’s <strong>in</strong>itial<br />
behaviour. Direct manipulation of coord<strong>in</strong>ation to improve performance<br />
requires great care, however, <strong>and</strong> the swimmer should <strong>in</strong>itially work<br />
at adopt<strong>in</strong>g the imposed behaviour without try<strong>in</strong>g to improve performance.<br />
For example, if superposition coord<strong>in</strong>ation is the target coord<strong>in</strong>ation,<br />
the swimmer may <strong>in</strong>crease his stroke frequency, thereby slipp<strong>in</strong>g<br />
through the water without achiev<strong>in</strong>g the expected performance. When<br />
coaches directly manipulate coord<strong>in</strong>ation, they therefore need to keep <strong>in</strong><br />
m<strong>in</strong>d the importance of ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>g the same performance level.<br />
The follow<strong>in</strong>g sections present the similar behaviours <strong>and</strong> ma<strong>in</strong> differences<br />
between expert <strong>and</strong> non-expert front crawl swimmers regard<strong>in</strong>g<br />
(i) the effects of swim speed, active drag <strong>and</strong> energy cost; (ii) the<br />
relationships between coord<strong>in</strong>ation, propulsion <strong>and</strong> efficiency; (iii) the<br />
relationships between coord<strong>in</strong>ation <strong>and</strong> performance, bear<strong>in</strong>g <strong>in</strong> m<strong>in</strong>d<br />
that coord<strong>in</strong>ation may be either flexible or stable; <strong>and</strong> (iv) the effect of<br />
breath<strong>in</strong>g, which suggests that swimmers organise their limb coupl<strong>in</strong>g<br />
not only to propel but also to breathe <strong>and</strong> float.<br />
coordInAtIon, sWIM sPeed, ActIVe drAG And enerGY<br />
cost<br />
Accord<strong>in</strong>g to Newton’s second law ( ∑ F = m. a , where F is the force, m<br />
the mass <strong>and</strong> a the acceleration), forward body displacement is related<br />
to the differences between the propulsive forces generated by the swimmer<br />
<strong>and</strong> the aquatic resistive forces (i.e. the environmental constra<strong>in</strong>ts).<br />
36<br />
In fact, forward body displacement seems to be a more complex process<br />
<strong>and</strong> the swimmer may cross several solutions, probably the production of<br />
propulsive forces, the m<strong>in</strong>imization of active drag, the maximization of<br />
propulsive efficiency (i.e. m<strong>in</strong>imization of k<strong>in</strong>etic energy) <strong>and</strong> the monitor<strong>in</strong>g<br />
of <strong>in</strong>ter-limb coord<strong>in</strong>ation.<br />
Thus, when active drag <strong>and</strong> speed (active drag changes with speed<br />
squared) <strong>in</strong>crease, <strong>in</strong>ter-limb coord<strong>in</strong>ation is affected, particularly by a<br />
decrease <strong>in</strong> the time lag between two propulsions, which means that<br />
the relative duration of the glide <strong>and</strong> catch phases decreases. In front<br />
crawl, Chollet et al. (2000) <strong>and</strong> Seifert et al. (2004, 2007b) showed that<br />
speed <strong>in</strong>creases lead to similar motor behaviour <strong>in</strong> expert male, expert<br />
female, <strong>and</strong> non-expert male swimmers: they <strong>in</strong>crease the IdC <strong>and</strong> simultaneously<br />
<strong>in</strong>crease stroke rate <strong>and</strong> decrease stroke length. Seifert et<br />
al. (2010b) used an arms-only protocol both on the Measur<strong>in</strong>g Active<br />
Drag (MAD) system to assess active drag dur<strong>in</strong>g an <strong>in</strong>cremental test<br />
<strong>and</strong> while swimm<strong>in</strong>g <strong>in</strong> free condition to assess <strong>in</strong>ter-arm coord<strong>in</strong>ation<br />
<strong>in</strong> front crawl. They showed a l<strong>in</strong>ear regression between active drag <strong>and</strong><br />
IdC (0.64 < R² < 0.98), confirm<strong>in</strong>g that swimmers have to modify their<br />
motor organization when the task (speed) <strong>and</strong> environmental (drag)<br />
constra<strong>in</strong>ts <strong>in</strong>crease.<br />
Similar results were found when energy cost <strong>in</strong>creased: reach<strong>in</strong>g<br />
higher speed leads to higher energy expenditure <strong>and</strong> <strong>in</strong>creases IdC <strong>and</strong><br />
stroke rate (Morais et al., 2008; Seifert et al., 2009).<br />
coordInAtIon, ProPulsIon And eFFIcIencY<br />
Only expert swimmers atta<strong>in</strong> high speeds, as they are able to generate<br />
high power output <strong>and</strong> reach high IdC. Indeed, when expert swimmers<br />
<strong>in</strong>crease their speed <strong>and</strong>/or their stroke rate above a critical value (respectively<br />
~1.8 m.s -1 <strong>and</strong> 50 stroke.m<strong>in</strong> -1 ), only the superposition mode<br />
is observed (Potdev<strong>in</strong> et al., 2006; Seifert et al., 2007b), which may be<br />
attributed to the dom<strong>in</strong>ance of wave drag. When mov<strong>in</strong>g at high speed<br />
<strong>in</strong> whole stroke (> 1.5-1.7 m.s -1 ), wave drag becomes even greater, account<strong>in</strong>g<br />
for up to 50-60% of total drag (Toussa<strong>in</strong>t & Truijens, 2005;<br />
Vennell et al., 2006). Us<strong>in</strong>g a process similar to the calculation of “hull<br />
speed” for a ship, the authors mentioned above found that the hull speed<br />
for a swimmer with an arbitrary height of 2 m was 1.77 m.s -1 (Toussa<strong>in</strong>t<br />
& Truijens, 2005). This f<strong>in</strong>d<strong>in</strong>g co<strong>in</strong>cides with the large <strong>in</strong>crease <strong>in</strong> active<br />
drag found above this critical speed (> 1.7-1.8 m.s -1 ), as determ<strong>in</strong>ed<br />
by the wave drag, the environmental constra<strong>in</strong>ts elicit<strong>in</strong>g a superposition<br />
coord<strong>in</strong>ation of the arms. Indeed, it was recently shown that an<br />
<strong>in</strong>crease <strong>in</strong> speed leads to simultaneous changes <strong>in</strong> drag force, power<br />
output <strong>and</strong> <strong>in</strong>ter-arm coord<strong>in</strong>ation. While swimm<strong>in</strong>g only with arms<br />
<strong>in</strong> the free swimm<strong>in</strong>g condition, expert front crawl swimmers switch<br />
the <strong>in</strong>ter-arm coord<strong>in</strong>ation from catch-up mode (IdC < 0%) to superposition<br />
mode (IdC > 0%) above a speed of 1.5-1.6 m.s -1 at maximal<br />
<strong>in</strong>tensity (Seifert et al., 2010c). Us<strong>in</strong>g arms-only on the MAD system,<br />
the same swimmers exhibited a drag force of 100-110 N at maximal<br />
<strong>in</strong>tensity, develop<strong>in</strong>g a mechanical power output of ~200 W (Seifert et<br />
al., 2010c). Conversely, less-expert swimmers also swimm<strong>in</strong>g at maximal<br />
speed exhibited a drag force < 100 N, power output < 180 W <strong>and</strong> <strong>in</strong>terarm<br />
coord<strong>in</strong>ation <strong>in</strong> catch-up mode (IdC < -6%), which did not enable<br />
them to reach the same speeds as the expert swimmers. On the other<br />
h<strong>and</strong>, a high IdC does not guarantee high speed, as the swimmer can<br />
slip through the water <strong>and</strong>/or spend a long time <strong>in</strong> the propulsive phase<br />
because of slowed h<strong>and</strong> speed, mean<strong>in</strong>g low propulsive efficiency. Notably,<br />
Seifert et al. (2010b) showed that IdC <strong>in</strong>creases with active drag<br />
<strong>in</strong> experts, but that at maximal <strong>in</strong>tensity (swimm<strong>in</strong>g 25m all out) IdC<br />
is not correlated with propulsive efficiency for this sample of swimmers.<br />
Moreover, when speed <strong>in</strong>creased, expert swimmers <strong>in</strong>creased IdC while<br />
their hip <strong>in</strong>tra-cyclic speed variation rema<strong>in</strong>ed stable with a coefficient<br />
of variation close to 0.15 (Schnitzler et al., 2008; Seifert et al., 2010c).<br />
Conversely, non-expert swimmers did not significantly change their<br />
arm coord<strong>in</strong>ation (which rema<strong>in</strong>ed <strong>in</strong> catch-up mode) while their hip<br />
<strong>in</strong>tra-cyclic speed variation <strong>in</strong>creased (from 0.16 to 0.21). These results<br />
suggest that, unlike non-experts, expert swimmers make effective motor