There are many factors determining high physical endurance in young swimmers. The influences of somatic indices are among them. Indices of physical fitness on swimming speed have been under examination for many years as these parameters, which with swimming technique, directly determine the ability of high performance swimming (de Mello Vitor and Silveira Böhme 2010; Geladas et al., 2005; Lätt et al., 2010; Morouco et al., 2011; Reis et al., 2010; Strzala and Tyka 2009).

Swimming technique, especially the breaststroke, requires a talented swimmer with years of training. In improving swimming results it is very useful to use the information from the movement technique analysis of the individual swimmer and the high level peer group and compare an individual with the results of the whole group. Breaststroke swimming and its relationship with the physical performance of the swimmers seems obvious, in the breaststroke, as in no other competitive swimming technique, effort is devoted not only to the production of propulsion, but also in overcoming the resistance of water in the recovery phases of upper and lower limbs. After recovery, the glide and relaxation time occurs within each cycle, but its duration from a bio-mechanical and swimming efficiency point of view is disadvantageous due to increasing inter-cyclic velocity variation (Leblanc et al., 2005). These cyclic circumstances related to glide in sprint breaststroke swimming are different, the propulsive and recovery phases occur almost continuously without gliding, but it is paid for by a faster growth of fatigue (Komar et al., 2014; Strzala et al., 2013).

Adjustment of movement technique to produce a large amount of power and to minimize the resistance is always at the centre of a swimmers interest (Leblanc et al., 2007; Seifert et al., 2010). Analysis of swimming technique strategies that adapt to rising fatigue during the race and its separate parts is of interest to and useful for coaches (Arrelano et al., 1994; Chatard et al., 2001; Strzala et al., 2005; Thompson et al., 2000).

Considering the above mentioned remarks, observations regarding the influence of a swimmers body structure, as well as their ability to perform aerobic (Lätt et al., 2010) and anaerobic work (Reis et al., 2010), on breaststroke swimming speed and on the shaping of swimming parameters at the distance of 200 meters (Thompson et al., 2000) are what is aimed to be obtained. In this race, high level components of aerobic and anaerobic sources are necessary in order to cope with the breaststroke. This technique is loaded with higher water resistance like in no other race swimming. This is due to a less economic underwater recovery of arms and legs, which crates drag (Chollet et al., 2004; Kolmogorov and Duplishecheva, 1992). Higher resistive recovery forces during recovery in conjunction with cyclical changes of trunk angle attack on incoming mass of water (Conceicao, 2013), increases neuromuscular fatigue (Conceicao, 2014).

The aims of this study were: (a) to examine the influence of selected indicators of somatic properties and physiological capacity on the swimming speed in the 200-meter breaststroke race, (b) analyze kinematic parameters of breaststroke swimming as well as assessing their impact on the speed in the 200-meter breaststroke race and (c) test the level of contribution of clear surface breaststroke and turning zones swimming in the 200-meter breaststroke race.

We may hypothesize that in our research group physiological capacity indices play a greater role than the selected breaststroke kinematic parameters which are usually related to the efficiency and economy of propulsion movements. We expect that in short course racing the swimming in turning zones may have a similar or stronger influence on the 200-meter results than in pure surface breaststroke.

Swimming speed in the 200m (V₂₀₀) race was 1.22 ± 00.8 (m^.s^-1), surface swimming speed (V₂₀₀surface) in sectors between 10^th to 20^th meters of each successive pool of 200 m reached 1.09 ± 00.8 (m^.s^-1), while the breaststroke turn zone speed (V₂₀₀turns) result was the highest 1.27 ± 0.07 (m^.s^-1) powered by push of the each turning wall with stroke, during which the swimmer may be submerged. The physiological index levels achieved in the 90 sec. all-out anaerobic work capacity tests influenced the swimming speed. In testing, the relationship between indicators TWAR and V₂₀₀ as well as between VO_2peakLG and V₂₀₀surface (Table 1), the partial correlations (when controlled for age) were supplemented with Cohen (f²) calculations. In both cases, the resulting effect-size indexes were large, the first value being f² = 0.75 and f² = 0.56 in the second case. It was then noted that V₂₀₀turns was significantly dependent on TWAR and VO_2peakLG. LBM index influenced significantly V₂₀₀turns (0.38, p < 0.05) and strongly interplayed with all physiological variables (Table 1).

Variants of surface pool swimming showed variations of surface pool swimming (F = 4.24, df = 7.208, p < 0.001), the results of Tukey’s post-hoc test showed that the 1^st lap was statistically different (p < 0.001), (Figure 1, left). Speed in successive turns was varied; however the statistical differences were between the first and the third, fourth, fifth, sixth and seventh turn (Tukey test p < 0.001). In spite of this a cubic trend was established for the curve (F = 7.54, df = 6.182, p < 0.001) (Figure 1, right). The V₂₀₀turns and V₂₀₀surface were strongly associated with V₂₀₀, 0.92, p < 0.001 and 0.91, p < 0.001 respectively.

Basic stroke kinematics SR and SL complement each other in successive measurements. SR decreased on the second 50m than increased on the third and fourth 50m, conversely shaped the SL indices, however, their diversity was not statistically significant (Figure 2).

The TTG index of the breaststroke cycle non-significantly decreased, while the percentage of arm propulsion in the cycle (AP) increased, but non-significantly. The less dispersed variable of LP increased with statistical significance in a linear trend (F = 29.82, df = 1.104, p < 0.001) (Figure 3). A scatter chart shows the Glide or Overlap coordination movement index in which individual cases were the most dispersed, the value of the index was similar in the first part of the 200m, then increased, but without significance (Figure 4).

There was a statistically significant effect between the indicators of swimming techniques listed in Table 2, it is between V 200surface and LP, LR indices.

The main aim of this study was to examine the selected indicators of somatic properties and physiological capacity, and analyze kinematic parameters of breaststroke swimming as well as assessing their impact on the breaststroke swimming speed.

In our observations the V₂₀₀ was moderately dependent on VO₂peakLG, moreover, separate V₂₀₀turns depended on VO₂peakLG and on LBM and TWAR. The body’s functional capacity has an important impact on achieving good breaststroke swimming results in the young swimmer. Reis et al. (2010) researched the combination of aerobic fraction on energy release, peak blood lactate post-exercise and VO₂ elicited at the swimming velocity corresponding to 2 mmol·L^-1 explained optimum season event performance for the 200 m breaststroke. Peak level of VO₂ obtained in the all-out tests lasting for approximately one minute can be a good predictor of a swimmer’s physical endurance during their efforts (Brickley et al., 2006) even at a distance of 100 meters, as produced by mechanical work achieved using aerobic power (besides anaerobic capacity), which has a significant contribution of up to 54% in an effort lasting 90 seconds (Serresse et al., 1988). According to Withers et al., (1991) the rate of aerobic metabolism in maximal efforts lasting 30-s, 60-s and 90-s increases from 28% through 49% to 64%. The level of VO₂ in the last 30 seconds of maximal effort lasting 90 seconds may exceed 90% of VO₂max (Carey and Richardson, 2003), a level of even 98,7% was observed in the research of Withers et al. (1991). Lätt et al. (2010) reported similar results to ours, with a 3.51 l^.min^-1 VO₂ measured during maximal front crawl swimming at a distance of 100 meters, with a similar level of statistical association (partial correlation) to swimming results, although peak VO₂ has been found with higher correlations with 100-m speed (r = 0.787) in adult swimmers (Rodriguez et al., 2003). In studies of Lätt et al., (2010) a slightly higher level of dependence of swimming efficiency with LBM was reported, this index in our observation strongly determined the level of both TWAR and TWLG as well as VO_2peakAR, on the other hand VO_2peakLG, LBM and TWAR influenced V₂₀₀turns with statistical significance.

In this research V₂₀₀turns was strongly correlated with V₂₀₀, which is caused by the fact that swimming in the turn zones is one of the most important components at the distance of 200 meters, particularly in the short course. In short courses it can occur that up to 40% of the total event time is spent turning (Thayer and Hay, 1984), currently it is similar, although the swimming speed during turns has increased due to improvements in swimming technique and accordance with the rules of the execution of additional dolphin kick. The dependence noted by us was very strong, and swimming in the turn zones played a more important role than mentioned before, particularly within the (5m + 10 m) 5m distance of approaching the wall and 10m departure phase from the wall (Haljand, 2014). In other research Blanksby et al. (1998) noted that swimmers crossed the distance (5m + 5m), which gives 20% of the distance of 50 meters in 18.26 % of the mean 50 m breaststroke time. From the stepwise regression equation results they could state that it was advantageous for “…a taller swimmer who pivoted rapidly on the wall, generated a high peak horizontal velocity, and traveled an optimal distance underwater before surfacing at a relatively fast velocity” when attempting to achieve the best turn zone performance. Keskinen et al. (2007) points out that increased velocity after each turn in the front crawl has a period of relative inactivity during which the swimmer has time for recuperation. We have identified other findings which have shown that in breaststroke swimming this effect is even greater (Craig, 1986). Whereas in the, approximately, 10 m underwater displacement this relative inactivity during one arm stroke, single dolphin kick and the first arm stroke followed by a breaststroke kick is higher. In the research of Thompson et al. (2000) conducted on international top level elite breaststroke swimmers, there were moderate interrelationships reported between turning time (7.5 m+ 7.5 m) and 200 m time (-0.54, p < 0.01), however it was in a long course with three turns, where the velocity decreased in each turn but there was statistically insignificant difference between the second and third turns. In our observations a statistically significant cubic trend was noted for the curve representing the turn zones speed, and movement efficiency during turns depended on the swimmers’ physical efficiency TWAR, VO₂peak and LBM.

Another important result of this study was the ability to swim fast on the surface was positively and significantly associated with the percentage time of propulsion generation -LP in the breaststroke cycle, which is interesting; the non-propulsive phase –LR of the legs, including gliding, was negatively correlated to V₂₀₀surface. The ability to perform efficient propulsive leg movements brings the greatest propulsive benefit in every single cycle in the breaststroke amongst all styles (Kippenhan, 2001; Maglischo 2003; Mason et al., 1989; Strzala et al., 2012; Vilas-Boas 1994) analysed that swimmers accelerated their bodies for a longer time with their arms than they did with their legs and our results are in agreement with this. The kick is clearly the dominant propulsive force in the breaststroke, because swimmers accelerate the body forward much more strongly with their legs than arms, even though peak velocities are similar during other phases of the of the stroke (Maglischo, 2003).

In our observation we did not find significant dependence between percentage of propulsive arm movement and V₂₀₀surface. A more detailed division into phases, for example: catch, outsweep, and insweep, could provide a better idea of the shape of these phases (Payton and Bartlett, 1993; Strzala et al., 2013; Tourny, 1992).

The shape of the basic kinematic indicators SR and SL in the four segments of distance in our young swimmers were similar to those top level elite breaststroke swimmers (Hellard et al., 2008; Thompson et al., 2000, 2004;) and, although their values were lower, they overlapped even more with increasing distance, i.e. as SL decreased, SR increased on the 3rd and 4th 50m sectors of the total 200m. In the above mentioned analyses a statistically significant dependence between SL and V200 (0.36) was noted (Thompson et al., 2000). The data from their further study (Thompson et al., 2004) and later study by the Hellard team (2008) provided evidence that increases in both stroke rate and length cause an increase in swimming velocity in national and international 200 m breaststroke races. We agree with this statement, especially in the case of young swimmers who need master their efficiency by improving stroke length (Wakayoshi, 1995) and stroke rate (Yanai, 2001). We understand the importance of gliding ability (Barbosa et al., 2012; Leblanc et al., 2010) especially in longer 200m distance, but remember that this phase is only resistive. There is additional indication that true improvement in performance is generally achieved by prioritizing training and a swimmer’s competency for increasing three key variables: mid-pool swimming velocity, turn times and start time (first 15 m), but coaches should always compare their swimmers’ performance in each of these elements against their relative ranking before making a final decision on where to place training emphasis (Thompson et al., 2004).

The dependence between Glide, Overlap or TTG and V₂₀₀surface being statistically insignificant, shows the tendency of faster swimmers to limit the non-propulsive glide phase, which makes our results closer to those of Leblanc et al. (2007), where better swimmers reached 22% glide in comparison with less skilled (no recreational) who achieved more than 27%. Changes in the coordination indices in the following 50th m was related mainly to a decrease in glide phase, which is well recognized as a differential in shaping the movement cycles between sprinting and swimming a longer distance (Komar et al., 2014). For longer distances increasing propulsive force in the breaststroke cycles on the consecutive laps is achieved by an increase in SR, which correlates strongly with the Glide or Overlap, AP and LP indices (Strzala et al., 2013) and occurs with increasing fatigue (Conceicao et al., 2014). This happens gradually and proportionally to the loss of power, such as loss of power accompanied by our swimmers, or other athletes, in such all-out test as 90 sec. TWLG and TWAR.

In conclusion the above mentioned results indicate that the V₂₀₀ was directly dependent on two indicators of physiological performance VO_2peakLG and TWAR (f² = 0.54), however, after splitting the 200m breaststroke race for the most important components – surface (V₂₀₀surface) and – turning zones (V200turns) swimming showed the increasing significance of the physiological properties of the swimmers organism. V200turns in young swimmers depended significantly on indicators of physiological performance and body structure: TWAR, VO_2peakLG and LBM, LBM which in turn strongly determined the measured results of TWAR, TWLG, VO_2peakAR and VO_2peakLG. Whereas, V200surface depended on VO_2peakLG with large Cohen effect-size (f² = 0.75) and was significantly relative to the percentage of the leg propulsion - LP. During the successive laps of the 200m breaststroke swimming there was an increased percentage of propulsion production in the breaststroke cycles, occurring simultaneously with a reducing gliding phase. In addition, the indicators shaping: SL, SR, TTG, Glide or Overlap with increasing fatigue indicates a decrease in efficacy in propulsive movements.

The collected data indicates a significant role of the properties of the body and physical endurance indicators, which was particularly highlighted by their influence on the main component, V200turns, in the 200m breaststroke in the short course race. This knowledge may be an indicator for achieving better performance through its implementation in our or other swimmers.