Lower Body
Characteristics
Calf strength and hip flexibility both
play important roles in vertical jumping ability. Baechle and Earle
(2000) define flexibility as the range of motion about a body joint.
Moscov, Lacourse, Garhammer, and Whiting (1994) further define
flexibility as either static or dynamic. Static flexibility refers to
the maximum range of motion at a joint during a slow graded movement
and is limited by one or more connective-tissue structures, including
the joint capsule, muscle, tendon, and skin. Dynamic flexibility
refers to the maximum range of motion of a joint during a ballistic
movement. Dynamic flexibility has been a valid indicator of success in
ballistic sport activities (Moscov et al. 1994).
Moscov et al. (1994) investigated three groups
of ballet dancers; advanced level, intermediate level, and beginner
level to determine whether there were differences in static and
dynamic hip flexibility, leg power and leg strength. The test
administered for leg strength was the one repetition maximum on the
leg press machine. To determine leg power a vertical jump test was
performed. Static hip flexibility was measured by summing hip range of
motion during flexion and hyperextension. Dynamic hip flexibility was
determined while each dancer performed a jete, which is a springing
step from one foot to the other in which the leading unsupported leg
is thrust into the direction of the leap. Joint markers were placed on
the greater trochanter, lateral epicondyle and medial epicondyle to
facilitate video analysis of the angle of interest (Moscov et al.
1994).
The dancers completed a warm up and then
performed three exercises: plie, tendu, and grand battement, each
requiring 2-3 min. of work. Each exercise was completed on both sides
of the body. Next, the dancers performed the vertical jump protocol.
Three jumps were completed with the standing reach protocol. Lastly,
they performed the one repetition maximum on the leg press. The order
of exercises went from the least fatiguing to the most fatiguing. This
was so the vertical jump scores were not skewed by the intensity of
the leg press 1 repetition maximum (Moscov et al. 1994).
Moscov et al (1994) showed that there were no
significant differences between the three ability levels for dynamic
hip flexibility, leg power, and leg strength. However, there was a
significant difference in static hip flexibility between the advanced
group and the beginner group. Static hip flexibility between advanced
level dancers and beginners was related to the extent of ballet
training. In contrast, the extent of ballet training did not appear to
effect dynamic flexibility. Moscov et al. (1994) noted that dancers
devoted a large portion of time trying to improve static hip
flexibility but there appeared to be no justification for this if the
primary goal was to improve dynamic hip flexibility. There were no
differences in leg strength and leg power between the groups. This was
due to the inadequate overload of training. The load was not great
enough to elicit an increase in leg strength and therefore leg power.
There appeared to be no relationship between the amount of hip
flexibility a dancer has to vertical jump height (Moscov et al. 1994).
Common assumptions that the greater range of
motion athletes have in their joints; a greater level of performance
will result. Lee, Etnyre, Poindexter, Sokol, and Toon (1989)
investigated the 1986 United Stated National Olympic Festival
Volleyball team. They compared hip flexibility to jumping height of 24
men and 22 women. Vertical jump was measured using the Vertec jump
measuring device. The athletes performed a standing vertical jump and
an approach vertical jump. A stainless steel goniometer was used to
measure hip flexion. Hip flexion measurement was taken while subjects
were lying supine with the right leg maximally flexed and both knees
fully extended (Lee et al. 1989).
Lee et al. (1989) showed that there was a strong
relationship between the two jumping measures for both the men and the
women. A significant and positive correlation was calculated between
the approach vertical jump and hip flexibility in the men. For women
significant and negative correlations were found between standing
vertical jump and hip flexibility and approach vertical jump and hip
flexibility (Lee et al. 1989). The researchers showed that a positive
correlation supported that increased hip flexibility was related to
greater jumping height in men. The opposite occurred for the women.
The women with the least flexibility in their hips jumped the highest.
Clarity as to why this occurred is unknown. The only possibility the
researchers could determine was, that the anatomical differences
between men and women in the hip joint. The increased flexibility in
the hip joint benefited the men more so than the women. The women on
average had greater hip flexibility than the men (Lee et al. 1989).
Brown, Gorman, DiBrezzo, and Fort (1988)
conducted a study measuring the improvement in lower body explosive
power after a six- week training using three modes. The three modes
were selected to represent different portions of the wholistic
athletic training model. The three modes were static training,
performed one 30 sec. static effort combining hip an knee extension
using electronic, digital strength apparatus. The second mode was
dynamic training. The group performed three sets of 8-12 repetitions
on a leg press machine with two min. rest in between sets. The
resistance was set to near fatiguing levels. The third group was the
motivational vertical jump, the subjects were motivated to attain
their maximal jump for 10 successive repetitions. Subjects also
underwent a goniometric test, which measured hip flexibility as part
of their assessment.
The researchers showed significant increases in
anaerobic power for the dynamic and motivational vertical jump groups
(Brown et al. 1988). There was little relationship between flexibility
and anaerobic power. Therefore, the researchers Brown et al. (1988),
Lee et al. (1989), and Moscov et al. (1994) had similar findings. Hip
flexibility had little if not any relationship to vertical jump with
the exception of Lee et al. (1989) men had a relationship between hip
flexibility and vertical jump, the women did not.
The calf muscle (gastrocnemius) plays a
major role in jumping ability. Stern (1991) stated that because the
ankle is a hinge joint, the ankle allows movement from a maximum
dorsiflexion of 20 degrees through neutral to a near maximum plantar
flexion of 50 degrees. Because of this, the ankle allows the calf
muscle work when fully contracted and not transfer the stress to the
bones. The calf is mostly composed of type II muscle fibers (fast
twitch). The calf flexes the knee and plantar flexes the ankle. When
the knee is bent the contractability is less in the calf and the
soleus muscle is responsible for extending the foot. The soleus is
made up of mostly type I (slow twitch) muscle fibers (Stern, 1991).
Signorile, Duque, Cole, and Zink (2002)
compared the muscle utilization patterns of two major muscles in the
triceps surea group during performance of multiple high speed constant
resistance exercise performances. The two muscles were the soleus and
the gastrocnemius. The gastrocnemius was divided into the lateral head
and the medial head. The researchers also examined the antagonist
muscle group called the tibialis anterior. Signorile et al. (2002)
stated:
The muscles of the triceps surae group differ in
their structure, anatomical position, function, and fiber type
characteristics. There differences may dictate different utilization
patterns among the muscles in the group. Structurally, the
gastrocnemius is a bipennate muscle, whereas the soleus is a fusiform
muscle. Anatomically the medial and lateral heads of the gastrocnemius
have their origins on the posterior surfaces of the
medial and lateral femoral epicondyles, respectively. In contrast, the
origin of the soleus is along the upper two thirds of the posterior
surfaces of the tibia and fibula. However, both muscles share a common
insertion on the posterior surface of the calcaneus via the Achilles
tendon (p. 434).
Signorile et al. (2002) stated that
because of the position of these muscles, they shared the common
action of plantar flexing the foot. The gastrocnemius also helps in
the action of flexing the knee because it passes across the knee
joint. Therefore, when the knee is bent, the gastrocnemius is less
effective when plantar flexing the foot when the knee is bent as
compared to when the knee is extended (Signorile et al. 2002).
Since the gastrocnenius has two heads;
lateral and medial, they too have different functions. The medial head
is of larger size and the origin is closer to the midline of the knee
joint and slightly more dorsal that the lateral head. The lateral head
has more sarcomeres than the medial head, and therefore the two have
different length-force relationships (Signorile et al. 2002). The
lateral head is comprised of 49% slow twitch muscle fibers and the
soleus is comprised at approximately 80%. Therefore, the gastrocnenius
can produce faster and more explosive movements. The soleus is more
endurance oriented and can sustain low intensity, long duration
activities (Signorile et al. 2002).Signorile et al. (2002) had 11
subjects perform three sets of 50 isotonic plantar flexions on a
Biodex dynamometer using three different knee angles. The knee angles
were 90, 135, and 180 degrees. Both the root mean square amplitude and
the integrated signal of electromyography (EMG) were analyzed to
quantify the level of activity in the muscles. The EMG reflects motor
unit recruitment, firing rate, firing duration, and propagation
velocity (Signorile et al. 2002).
Signorile et al. (2002) showed that
there were significant differences among the muscles at the different
angles. At 90 and 135 degress the tibialis anterior produced a lower
level of electrical activity than the other muscles. At 180 degrees
the medial head produced significantly higher root mean square
amplitude EMG values than the soleus and the tibialis anterior, but
the lateral head was not significantly different. Among the different
knee angles there were no significant differences for either the
tibialis anterior of the lateral head. There were significant
differences for the soleus and the medial head (Signorile et al.
2002). The soleus produced less activity at 180 degrees than at 90 and
135 degrees and the medial head produced greater activity at 180
degrees than at 90 and 135 degrees. The researchers showed similar
findings with the integrated signal EMG. Signorile et al. (2002)
stated:
The results of the EMG analysis of the medial
head, lateral head, and soleus muscles reveal notable differences in
muscle utilization patterns because of the knee angle. Because the
lateral head and the medial head cross both the knee and the ankle
joints, their length and relative tension during plantar flexion
would be affected by the changes in knee angle (p. 438).
The soleus has little effect on the knee angle
because of its origin. Therefore, the only impact that might be
expected due to the change of knee angles would be with the lateral
and medial heads of the gastrocnemius (Signorile et al. 2002). Taking
this information and using it practically, one would say to train the
gastrocnemius with the knee angle at 180 degrees and to train the
soleus with a knee angle at 90 degrees (Signorile et al. 2002).
The information provided by Signorile (2002)
helps further understand the research performed by Fukashiro and Komi
(1987). They examined the joint movement and the mechanical power of
the lower limb during three types of vertical jumps. The three jumps
were a maximal vertical jump from a squatting position, a maximal
vertical jump from an erect position with a countermovement, and
repetitive submaximal hopping in place with preferred frequency. The
jumps were filmed with a 16 mm cine-camera from a side view. The
vertical ground reaction forces were taken for analysis. After
analyzing the three jumps, the countermovement jump represented a
large amount of force in sequence from the hip, then the knee, and
then the ankle. The squat jump was similar to the countermovement but
to a lesser degree at the hip. The order of force application was the
same as the countermovement jump. The hopping was very different from
the squat and countermovement jumps. The largest force came from the
ankle, next was the knee, and the smallest was the hip joint.
Fukashiro and Komi (1987) showed that the movements in the squat jump
and the countermovement jump depended primarily on the hip extensors,
whereas the hopping movement depended on the ankle plantar flexors (soleus,
gastrocnemius, tibialis posterior, peroneus group, flexor digitorum
longus, and flexor hallucis longus). The mechanics of the hop signify
the last phase of the vertical jump. The researchers, Signorile et al.
(2002) and Fukashiro and Komi (1987), and Stern (1991) illustrate that
the calf muscles play a big role in vertical jumping ability.