The high value of the standard deviation quotient (Table 3) is the main indicator of the quality of the monofin swimming model created by the network. The similarity between the values of quotients and errors in the teaching and validation tests are also apparent. This indicates the importance of the constructed model to real life swimming conditions. The diagnostic value of the parameters indicated by the Artificial Neural Networks can also be interpreted through the error values. On this basis one can conclude that if the most significant parameters, which described the angular accelerations of the proximal and distal parts of the fin as well as the entire monofin’s surface attack, are not taken into account, the diagnostic value of the model decreases by 22%-31%. This argument implies that the network was chosen properly for the process analyzed, and that the model may be used to assess the monofin swimming technique. Among the parameters defined by the network the angle of attack and the angles of monofin flexion are crucial for achieving maximal swimming speed. The angle of monofin flexing at a given point is defined by angles of attack of its parts in relation to this point. Positioning of the monofin in relation to the feet was interpreted in a similar way. The angle of attack was classified as a factor determining position in relation to swimming direction (movement trajectory) and the direction of the water flow around the surface (monofin shape). The optimum range of the angle of attack ensures the effective use of the propulsive force components (Schleichauf, 1979; YI-Chung and Hay, 1998). In unsteady flow, the trajectory and the shape of the monofin play a dominant role in inducing surface vortex (Ungerechts et al., 1999). Within the proportional correlation between the angle of attack and the vorticity of the vortex - the Magnus Effect and Bernoulli’s Theorem explain the development of an additional lift force component. In certain parts of the cycle (Figure 5, sequences 2, 3, 4) this acts in opposition to the swimming direction, thus creating propulsion. Swimming speed is the result of positioning the monofin at a proper angle of attack and angle of flex in order to make use of the horizontal components of the reaction acting in opposition to the swimming direction (Rejman et al., 2003a). Comparisons between the propulsive movements of monofin swimming and those of fish confirm the importance of lift and thrust in effective propulsion (Daniel, 1984; Wolfgang and Anderson, 1999). When interpreting the propulsion of the monofin based on mechanism action - reaction is not limited to the use of thrust and lift - the angle of attack and the angle of flex determine the direction of movement of added water mass. When pushed backwards (Figure 5, sequences 2, 3, 4) this creates an additional source of propulsion (Colman et al., 1999). Equating the velocities of points on the monofin with force recorded in those points is the result of the relation between drag and velocity (Rejman et al., 2003b). Therefore, the moment of force bending the monofin is a product of the force of reaction (measured in selected points on the monofin’s surface) and its arm (the length of the parts of the monofin). The model can be represented by formulas describing dependencies between the momentum of the bending forces and the examined parameters, i.e. angle of attack, angle of flex (Equations 1, 2), angular velocity (Equation 4), angular acceleration of attack and flexing (Equations 3, 4), and momentum of reaction force recorded in the tail and in the middle of the monofin (Equations 2, 3, 4). In conditions of unsteady flow: The results (Figure 5, 6">6) support the mechanism arising from interpretation of the model at level I. In the first part of the downbeat (Figure 5, sequences 11-1), horizontal velocity of the swimmer increases. In the second part, the increase of this velocity is lower (Figure 5, sequences 1-2). Flexion increases the angular velocity of leg and foot movement when the legs are extended and ‘extends’ the scope of force transferred to the monofin. In effect, the angular velocity of the legs increases together with the force of tail flexing. The dynamics of tail flexing stimulate swimming speed changing the shape of the monofin at the point of transfer of force, generated by the legs, to the monofin. Dorsal flexion of the feet affects the changes in the angle of attack. The resulting angle of attack positions the remaining part perpendicular to the swimming direction. Acceleration increases the mass of water circulating backwards and pushes the monofin back (Colman, et al., 1999). This complements the lift component. Part of the energy expended on accelerating the water mass is recovered thanks to the shortening of the time needed to generate propulsion. The first phase of the upbeat is similar (Figure 5, sequences 6-8). The increase of the swimmer’s horizontal velocity is lower than in the downbeat due to knee flexion. The monofin moves in line with the movement and does not generate propulsion. In this situation the intensification of acceleration of thigh movements does not flex the tail, ensuring proper positioning, as the proximal part of the monofin does not allow for positioning the distal part of the fin perpendicular to the swimming direction. Part of the energy expended is through decreased water resistance closest to the fin resulting from water circulation at the surface of the monofin. Additionally, upbeat acceleration ‘pushes’ the swimmer forwards (Colman et al., 1999). In sequences 3-4, horizontal velocity of the swimmer (vH) drops. Because of knee flexion, the mass of water slides off the monofin. The drop in the swimmer’s horizontal velocity is limited by the monofin’s flexible energy (the thighs start to move upwards at the end of the downbeat phase). A drop in horizontal velocity also occurs in sequence 8-10. This results from the adjustment of the monofin shape to the direction of water flow. The added mass of water slides from under the monofin as it is no longer being accelerated (Colman et al., 1999). Transition from the downbeat to the upbeat phase, results in a drop in horizontal velocity of the swimmer which is lower than the downbeat. At the end of the downbeat, part of the energy expended on pushing may be recovered when the mass of water near the edge of the monofin circulates in a direction opposite to the movement and ‘pushes’ it additionally from behind (Colman et al., 1999) (Figure 5, sequences 4-5). The minimum horizontal velocity of the swimmer was recorded in the last sequence of the upbeat (Figure 5, sequence 10,11) when the parallel positioning of both segments and the change of direction in movement do not constitute a basis for propulsion. Diagnostic checking of the model at levels II and III was based on the correlation between horizontal velocity of the swimmer and the model’s parameters directly influencing swimming speed (Table 2): angle of attack of the monofin’s entire surface, angular velocity and angle of the monofin’s distal part attack. The indirect influence of most parameters on speed is confirmed by the confrontation of model results with the significance of the correlation with forces flexing the monofin, presented in the Table 2. Theoretical and empirical proof of the results provides a basis for the search for practical solutions aimed at optimization of leg and monofin movement technique to achieve maximum speed. Adverse hydrodynamic conditions in the upbeat tend to minimize loss caused by adverse horizontal velocity of the swimmer changes due to this phase. Therefore, the upbeat seems to be an extra source of propulsion. The results suggest that the proximal and distal parts form reserves in the acceleration of attack. This is supported by the fact that the horizontal velocity of the swimmer depends on the dynamics of the upbeat (Rejman and Ochmann, 2005). Forces flexing the monofin are correlated with the acceleration parameters defined in the model. There are reasons to believe that the upbeat propulsion effect is dependent on constant angular acceleration. This is confirmed by the shorter time of increase in horizontal velocity in the upbeat than the downbeat phase. These generalizations are supported by the results of other studies. The power of leg movements in dolphin swimming drops proportionally to the change in velocity of those movements (Holmer, 1982). Avoiding sudden changes in the velocity of monofin affects the constant swimming velocity (Rejman, 1999). Propulsive movements with unstable velocity result in the creation of unsteady vortices and their uncontrolled distribution has a negative affect on the structure of propulsive forces (Arellano and Gavilan, 1999a). Therefore, the constant rotation of the vortex is a measure of advanced monofin swimming technique. This constant rotation (rhythm) results from the linear acceleration of velocity until the vortex breaks away from the monofin’s surface. (Wu, 1968; Vilder, 1993). Reserves in the upbeat may also be used in the reduction of the degrees of freedom of the legs (the limitation of the movements in knee joints and shin-ankle joints) and the controlling of the monofin’s flexibility, which fulfils a certain function in the process of propulsion. This thesis is confirmed by the analogy between monofin swimming and Tuna fish swimming (Colman et al., 1999). As a result of undulatory movements accompanied by wave resistance, the shape of the fin surface changes, causing a negative phenomenon. In order to minimize this, it is necessary to minimize the amplitude of monofin movements while increasing stroke length. Consequently, the delay in the transfer of moments of force generated by the leg muscles and the forces flexing the monofin, normally characteristic in this phase, does not occur (Rejman et al., 2004). At the current level of generalization, the optimization of leg and monofin movement technique is demonstrated in the extending of knee joints as quickly as possible in order to immediately flex the distal part of the monofin and therefore to position it perpendicular to the swimming direction. The continuation of the movement with maximum leg extension will allow extension of the amount of time a monofin of a given shape will move in the optimum trajectory, thus generating the maximum propulsion necessary to achieve maximum swimming speed. The theoretical and empirical (realistic) verification created by the parameters indicate by Artificial Neural Networks, paves the way to creating a more detailed deterministic model, and requires the application of its elements to other groups of swimmers. |