Page 1 of 19

European Journal of Applied Sciences – Vol. 12, No. 4

Publication Date: August 25, 2024

DOI:10.14738/aivp.124.17314.

Li, R., & Cui, W. (2024). Harnessing Active Force: The Pumping Mechanism of Child’s Swing Motion. European Journal of Applied

Sciences, Vol - 12(4). 164-182.

Services for Science and Education – United Kingdom

Harnessing Active Force: The Pumping Mechanism of Child’s

Swing Motion

Rong Li

Research Center for Industries of the Future, Westlake University, Hangzhou,

Zhejiang 310030, China and Key Laboratory of Coastal Environment and

Resources of Zhejiang Province, School of Engineering, Westlake University,

Hangzhou, Zhejiang 310030, China

Weicheng Cui

Research Center for Industries of the Future, Westlake University, Hangzhou,

Zhejiang 310030, China and Key Laboratory of Coastal Environment and

Resources of Zhejiang Province, School of Engineering, Westlake University,

Hangzhou, Zhejiang 310030, China

ABSTRACT

Life mechanics, an emerging field, focuses on the self-organizing motions

manipulated by the mind within living systems. This study introduces the concept

of 'active force’, generated by mind-body-environment interactions, as a

fundamental driver underlying these self-organizing movements. As an example,

we propose a new set of control equations to model the self-pumping swing

motion by incorporating the active force into Newton's second law. With this new

mechanical framework, we inversely derived the total (i.e., responsive) active

force due to the body-environment interaction from the child’s swing motions

with rapid standing and squatting movements. It revealed a pulse-like pattern of

the total active force along the swing length, driving changes in the radial speed

and swing length. This force counteracts the resistance and propels the swing,

which is not attainable by the stone. Consequently, the active force serves as the

foundational principle for self-organization in living systems, offering a novel

mechanical approach for understanding and predicting extraordinary movements

(e.g., sports and rehabilitation) regulated by the mind (e.g., nervous system) in

biological systems.

Keywords: Mind-body interaction, Active force, Newton's Second Law, Swing, Pulse

INTRODUCTION

Dyson, a physicist, remarked that the twenty-first century may be the century of biology [1].

Life, the most intricate of complex systems, is usually defined as a system that exhibits many

nontrivial movements, including responsiveness, energy transformation, metabolism, growth,

reproduction, and evolution [2]. Understanding these living movements poses the greatest

challenge in modern science [3, 4]. Accepting the axiom that force is the only reason for the

change in body movement, Schrödinger's seminal question "What is life?" [5] can be reframed

in the context of Newtonian mechanics: can we construct a mechanical model that describes

nontrivial movements inherent in life?

Page 2 of 19

165

Li, R., & Cui, W. (2024). Harnessing Active Force: The Pumping Mechanism of Child’s Swing Motion. European Journal of Applied Sciences, Vol -

12(4). 164-182.

URL: http://dx.doi.org/10.14738/aivp.124.17314

Traditional Newtonian mechanics, which views the human body as the mechanical sum of its

parts, overlooks the complexity of mind-manipulating interactions and emergent behaviors.

From the late 19th century, it became clear that viewing life merely as a machine was

insufficient for understanding phenomena, such as embryonic cell development. For instance,

Driesch's experiments suggest that cells have an inherent ability to adapt to changing

environments [6, 7]. Further studies led to the birth of the modern system theory in the 1930s

[8]. The “vitality” and “entelechy” postulated by early vitalists [9] found modern

interpretation in the concept of “self-organization” in complex system science [10, 11].

However, despite the development of numerous phenomenological differential equations and

theories for complexities and lives [11-15], mechanical descriptions of the dynamics of self- determined (i.e., by mind) movement in life remain rare. This void in physicists’

understanding signals the need for the development of life mechanics [16].

In response to this need, we propose the concept of "active force”, an internal force and its

direct response arising from mind-body-environment interactions, as an integral part of life

mechanics. Recently, studying the autonomous motions in living and engineering systems has

led to a conceptual innovation related to “active” mechanics, for instance, “active matter” in

physics [17] and “active cell mechanics” in biomechanics [18], reminiscent the “action

potential” in electrophysiology [19]. Therefore, the active force is a straightforward

conceptual development along this concept series to define the mechanical deriver of

autonomous motions, which ranges from cells, fish, birds, and people. Indeed, the concept of

active force has been mentioned in a minority of literature, for instance, in experimental

analyses of certain skeletal and muscular motions [20, 21] as well as in active cell mechanics

[18], where it acts as the (stochastic) force driving self-organization behaviors. However, its

mechanical study is still in its infancy, possibly due to its vague mechanical definition,

calculation, and measuring complexity.

Therefore, there remains a substantial gap in understanding the generation mechanisms,

temporal patterns, and physiological significance of the active force. To fill this gap, our new

general system theory (NGST) [22-25] begins a preliminary study into its generation

mechanisms, classification, and mechanical representation in Newton’s laws. It presents

unified mechanics incorporating this active force from mind-body-environment interactions

and the passive forces arising from external interactions with other objects or the inanimate

matter-matter interactions independent of the mind. In other words, whether the force is

active or passive only depends on whether it is generated by mind-body interaction. This

classification doesn't violate Newton's laws; thus, the concept of active force is not a violation

but rather an extension of classical mechanics to incorporate the dynamics of living objects

under the living state. Our previous work on NGST has also shown that the active force must

compensate for the energy dissipated by resistance in a changing environment through doing

work [26, 27].

In this study, we examined the dynamics of a simple pendulum system to illustrate the

necessity of an active force to explain the observed phenomena in swing motions. Specifically,

by comparing the motion patterns of a child and a stone of equivalent weight, we demonstrate

that an active force that extends beyond the conventional forces of gravity and friction is

introduced by a child to generate motion patterns that diverge from those of a lifeless swing.

Page 3 of 19

Services for Science and Education – United Kingdom 166

European Journal of Applied Sciences (EJAS) Vol. 12, Issue 4, August-2024

This difference originates from the mind manipulating internal interactions and relative

motions between elements (e.g., leg muscles in swing motion or walk) of the body, which

induce a subsequent extra body-environment interaction, propelling the center of mass

motions of the swing. Our findings underscore the importance of incorporating an active force

into Newton's second law and the mechanical analysis of the mind-body-environment

interaction as a fundamental paradigm in active life mechanics.

GENERAL FRAMEWORK OF NEWTON'S SECOND LAW WITH ACTIVE FORCE

Consider the mechanics of a particle within a multiparticle system situated in an Earth-fixed,

non-inertial coordinate system (as depicted in Fig.1). This model is grounded in the

perception that our planet is in motion, an understanding that dates back to the era of Galileo

Galilei. In this context, the governing equation for each particle is derived from Newton's

second law:

d

2

dt

2 miri = Fi

P + Fi

A + Fi

D

, (1)

where mi and ri are the mass and displacement vectors of the ith particle, respectively, Fi

P

, Fi

A

and Fi

D

are the passive-driven force, active force, and dissipative force, respectively. Note that

the vectors are indicated by Roman letters.

Fig. 1: A schematic representation of a N-body system in an earth-fixed coordinate system. It

means that we only consider the motions of the particle systems relative to the observer on the

earth.

Eq. (1) embodies Newton's axiom that force is the agent of the motion change. The dynamics

of nonliving objects can be adequately described by the passive-driven forces Fi

P

and

dissipation forces Fi

D

. These passive-driven forces were generated from other objects,

including particles and the earth, in the system we studied. The most common passive-driven

forces in the macroscopic world are gravity (Fi

G = GmM/r

2

) and the static electromagnetic

force, that is, Fi

M = qi(E + vi × B), where E is the electronic field, B is the magnetic field

strength, qi and vi = ṙ

i are the charge and velocity of the particle, respectively. These forces

Page 4 of 19

167

Li, R., & Cui, W. (2024). Harnessing Active Force: The Pumping Mechanism of Child’s Swing Motion. European Journal of Applied Sciences, Vol -

12(4). 164-182.

URL: http://dx.doi.org/10.14738/aivp.124.17314

can be expressed as a derivative of the generalized potential: Fi

P = −∇U + d(∂U/∂ṙ

i

)/dt,

where the generalized potential is U = VG + qφ − qA ∙ v. Here, VG is the gravity potential and

φ and A are the scalar and vector potentials of the electromagnetic field, respectively. This

analysis employs an Earth-fixed coordinate system and implicitly assumes the validity of

Newton's second law in a non-inertial coordinate system. According to the NGST ontology [26,

27], we must abandon the assumption of inertial coordinate systems because they do not exist

for human observers. However, the origin and expression of Fi

D

are typically complex. The

classical linear friction (Fi

D = −kivi

) and its corresponding Rayleigh dissipation function D =

∑ kivi

2

i /2 [28] is only a particular case (i.e., n = 1) of the general formula, that is, Fi

D = −kivi

n

.

Although complex, friction is always defined along the inverse direction of the velocity.

In addition, a new type of force, referred to as the "active force,” was introduced to explain the

initiating movement changes in living entities [22]. As introduced in the Introduction section,

the active force is the internal force directly generated by the mind-body interaction in a

living system. In contrast, the passive forces arise from external interactions with other

objects or the internal but inanimate matter-matter interactions independent of the mind.

Therefore, the critical distinction between active and passive forces is whether directly

generated by the mind-body interaction. Thus, any entity possessing a mind can exert an

active force; the separation of the mind from the body signifies the death of a living organism.

After death, a living object no longer exhibits an active force.

Thus, two immediate questions arise. How can the internal active force generate the center of

mass motions, and how can this active force be calculated? From our daily experiences,

humans exhibit active forces during their self-determined movements. For example, humans

and other animals can walk, run, and swing by using both the internal active force and the

body environment interactions. To generate these self-determined movements, one generally

utilizes the mechanism of mind-body-environment interaction: the mind issuing biosignal

(e.g., Nerve impulse) to modulate the interactions between elements of the body and their

relative motions. Subsequently, the body exerts extra force changes to the environment,

which in turn applies a reactive force that propels the body into the center of mass motion.

This tripartite interaction is essential to two kinds of active forces for the self-determined

movements of the living system. Compared to the baseline state of no motion or external

stimulation, we define the force change of the interactions between body elements as the

“internal active force” and the force change of the body-environment interaction as the

“responsive active force”. Thus, for each part of the body, we can obtain a decomposition of

the active force

Fi

A = Fi

I + Fi

R

, (2)

where Fi

I

is the internal active force and Fi

R

is the responsive active force. The mind-body

interaction mainly determines the former, while the environment constrains the latter.

Therefore, active force is interpreted as a mind-body-environment interaction. Without the

support of environment, the active force could not be generated.

Page 5 of 19

Services for Science and Education – United Kingdom 168

European Journal of Applied Sciences (EJAS) Vol. 12, Issue 4, August-2024

However, calculating these active forces is a significant challenge, as it is governed by the

unpredictable free will of the mind, as well as the complex mind-body-environment

interaction. We suggest initially adopting a model that explains this phenomenon qualitatively

and subsequently developing methods to quantify the active force. This study presented an

early effort and some initial results. In general, everyday human movements such as walking,

running, and swinging are inherently complex, necessitating rigorous modeling of the

interactions and movements of various body parts [29-31]. However, this paper aims not to

explore modeling too many complex motions but to clarify the differences between active

forces in living systems and those in inanimate bodies. Therefore, our primary focus in this

study was on the motion of the center of mass for its simplicity of degree of freedom and the

more straightforward measurement of the responsive active force compared to the internal

active force. In this case, the internal active forces of different body parts cancel with each

other (i.e., ∑ Fi

I

i = 0 following Newton’s third law), while the summation of the responsive

active force from the environment to the body is nonzero. Thus, in line with the definition of

the center of mass coordinates (R = ∑i miri / ∑i mi

), Newton’s second law can be obtained

from the summation of Eq. (1) as,

M

d

2

dt

2

R = Fp + Fa + f, (3)

where M = ∑i mi

is the total mass, Fp = ∑ Fi

P

i

is total passive (environment-to-body) force at

the baseline state of the body, f = ∑ Fi

D

i

is the total passive-driven force, total active-driven

force, and the total dissipation force, respectively. Fa = ∑ Fi

A

i = ∑ Fi

R

i

is the total active force

of the body relative to the baseline state, equaling the total responsive active force since

∑ Fi

I

i = 0. In this paper, we employ Eq. (2) to extract the total (responsive) active force

driving the swing's motion, deferring the elucidation of internal active forces to future

investigations.

THE RESPONSIVE ACTIVE FORCE FOR PUMPING A SWING BY A LIVING SYSTEM

This section explores how an active force propels a swing, mainly by comparing the dynamic

differences (displacement, velocity, and force) between the swing motions of a child and a

stone. This comparison enables us to quantitatively derive the temporal pattern of the

responsive active force, revealing the essential role of active force in explaining the motions of

living systems.

The Governing Equation for Pumping A Swing

Applying Eq. (3) elucidates the differences between the swing motions of a child and a stone,

considering only simple pendulum motions within a vertical two-dimensional plane. Fig. 2

illustrates the simple pendulum system: (a) represents a classical case with a non-living stone,

whereas (b) substitutes the stone with a child of equivalent weight. In the stone case,

L denotes the length of the rigid massless rod, m denotes the mass of the stone, and θ

represents the angle of the rod along the vertical axis. Furthermore, three forces acted at the

center of the mass of the stone. First, gravity, Fg = mg acts in the downward vertical direction.

Second, a passive tension force, Tp acts along the rod owing to the balance of gravity and

centrifugal force toward the frictionless pivot. Third, a friction force f resists the motion of

Page 9 of 19

Services for Science and Education – United Kingdom 172

European Journal of Applied Sciences (EJAS) Vol. 12, Issue 4, August-2024

37]. It can be considered as a coupled oscillator system composed of a swing and a human.

Typically, there are two pumping strategies: pumping from a standing position (as depicted in

Fig. 3) and a seated position. In the former instance, the person stands at the lowest point and

crouches at the highest point during the swing motion. Each stand-crouch cycle enhances the

swing amplitude. The analysis demonstrated that each crouch-stand cycle provides a swing

with an energy boost from the rider. In the latter scenario, the person abruptly rotates their

body around the end of the swing chain. The amplitude of the swing increases as these

rotations elevate the rider slightly above the highest level.

FIG. 3: Strategy for pumping a swing while standing, adapted from Ref. [38]. The child stands up

near the lowest point and crouches down near the highest point during the swing motion.

In the child’s swing motion, the mind determines the pumping strategies, while the active

force derives the body to motion, and environmental constraints provide the control

conditions for this driver; all these three factors of mind, active force and environmental

constraints are paramount. However, prior research on swing mechanics has primarily

concentrated on effective pumping strategies and environmental constraints, such as the

pumping mode (standing or seated [34, 38]), the modulation of frequency, and the initial

phase [37] under the swing constraints. On the other hand, the force underlying swing

pumping, particularly the active force that drives these movements, has been less explored.

This indicates that the essential force mechanism generated by the mind-body-environment

interaction— has not been adequately addressed. Our study aims to fill this gap by focusing

on the (internal or responsive) active force, which directly results from the mind-body- environment interaction and serves as the driver of the swing's active motion. This work

mainly focuses on the responsive active force, representing the body-environment

interaction. Understanding the temporal evolution pattern of this responsive active force is

crucial, as it not only reveals the direct capacity of individuals to drive the center of mass

movements but also how the environment responds to the body. Given that the force pattern

corresponding to the stand-crouch motion is simpler, we mainly concentrate on pumping

from the standing position in this study.

Page 11 of 19

Services for Science and Education – United Kingdom 174

European Journal of Applied Sciences (EJAS) Vol. 12, Issue 4, August-2024

δ(θ̇) =

d

dθ̇

H(θ̇) =

1

cb

1

2 + e

θ̇

cb + e

θ̇

cb

, (16 − d)

Here, ca determines the temporal pattern of standing up at the minimum angle, whereas cb

determines the temporal pattern of crouching down at the maximum angle. These two

parameters can be independently chosen according to the child’s free will.

The Responsive Active Force for Pumping A Swing Without Friction

By employing Eqns. (12)–(16), we can derive the time evolution of several parameters: the

angle θ(t), responsive active force Fa

, pendulum length L(t) = L0 + l(t), vertical height of the

mass center of the child h(t) = L0 − L(t) cos θ, the circumferential velocity v⊥ = L(t)θ̇(t) and

radial velocity v∥ = l(̇ t). The angle and velocities in two directions depict the dynamics of the

motion, whereas the alterations in swing length and height represent the spatial state. The

responsive active force, which is our primary objective, emerged from these calculations.

To execute this simulation, we must establish the parameters within these equations and

initial conditions. Let us assume that the masses of the individual and stone are identical, that

is, m = 20 kg. The swing's maximum pendulum length, L0, was 2 m, and the gravitational

acceleration g was 9.81 m/s

2

. We assume the height change of the child is k = 0.2m and zero

for the stone. The friction coefficient b, is influenced by the friction between the individual

and air, the swing, and between the swing rope and the fixed point.

Fig. 4: Active-motion simulations using Eqns. (12-16) for a child pumping a swing without

friction, as depicted by the solid red lines. In contrast, the dashed black lines represent the

simple pendulum motion of a stone with the same mass as the child. The parameters selected

for these simulations are outlined in Table I.

In our study, we account for the linear frictional force at low speeds between the child (or

stone) and the air, represented as f = −bv. The coefficient b is acknowledged to be variable,

Page 12 of 19

175

Li, R., & Cui, W. (2024). Harnessing Active Force: The Pumping Mechanism of Child’s Swing Motion. European Journal of Applied Sciences, Vol -

12(4). 164-182.

URL: http://dx.doi.org/10.14738/aivp.124.17314

contingent upon the changing conditions of interaction between the child (or stone) and the

air. Consequently, b is treated as a free adjustable parameter, facilitating a simplified and

flexible model that can adapt to a spectrum of realistic scenarios. The coefficients ca and cb,

which dictate the patterns of standing and crouching, as well as the initial angle θ(0) and

initial velocity θ̇(0) can be freely chosen by the child’s free will. Consequently, in this study,

we treat parameters b, ca, cb, θ(0) and θ̇(0)) as free adjustable parameters.

By substituting these parameters into Eqns. (12)– (16), we can juxtapose the swings of the

stone and the child. The simulations for the frictionless scenario are shown in Figure 4. As is

commonly understood, the stone (represented by dashed black lines) performs harmonic

oscillation, maintaining a constant amplitude throughout each period. Conversely, the child

(denoted by solid red lines) generates an enhanced oscillation, with the amplitude increasing

in each period. The figures show that the augmentation in the amplitudes of the angle (a) and

circumferential velocity (b) aligns with the continuous increase in radial velocity (e),

prompted by the child's periodically increasing responsive active force (d). This responsive

active force emerged as four pulses per cycle, corresponding to two standing and two

crouching instances. More specifically, during the first 1/4 period, the initial angles (a) and

initial circumferential velocities (b) for the stone and child were close. However, the child’s

swift standing motion around (see (d)-(f)) leads to a gradual increase in the angle and the

circumferential velocity, reaching peak differences from the stone around 2.0 s and 2.2 s.

Consequently, we conclude that in swing motion, the child's active force stimulates the

amplification of the swing's amplitude.

Table I: Parameters selection for the stone (zero active force) and the child (finite

active force) with zero friction.

System Mass Maximum

length

Gravitational

acceleration

Friction

coefficient

Standing

height

Pulse

angle

Pulse

velocity

Initial

angle

Initial

velocity

M(kg) L0(m) g(kg. s

−2

) b(kg. s

−1

) k ca cb(s

−1

) θ(0) θ̇(0)

Stone 20 2 9.8 0 0 — — π/6 0

Child 20 2 9.8 0 0.2 0.12 0.20 π/6 0

We proceeded with a quantitative analysis of the energy-pumping mechanism facilitated by

the responsive active force. In a frictionless environment, we assume that standing up and

crouching down are executed instantaneously. Because the responsive active force solely

impacts the radial motion, neither the circumferential momentum (or velocity) nor the angle

changes this process. The critical variables that vary are the pendulum length, which shifts

from L0 to L0 − k, and the radial velocity v∥ = l(̇ t). By examining the nth instance of standing

up, we can establish a relationship between the maximum swing amplitudes before (θn−1)

and after (θn) the actions. The law of energy conservation dictates that the circumferential

kinetic energy (m(v⊥

n

)

2

/2) at the lowest point originates from the potential energy decrease

(mgL0

(1 − cosθn−1

)) of the child from the maximum swing angle θn−1. After standing up, this

kinetic energy transitions into a potential energy increase (mg(L0 − k)(1 − cosθn

)) of the

maximum swing θn. As such, the potential energy decreases before standing up is equal to the

increase following it,

Page 13 of 19

Services for Science and Education – United Kingdom 176

European Journal of Applied Sciences (EJAS) Vol. 12, Issue 4, August-2024

mgL0

(1 − cosθn−1

) ≈ mg(L0 − k)(1 − cosθn

). (17)

From this relation, we can obtain the nth maximum angle, height, and velocity as:

θn ≈ arccos [

cosθn−1 − k

1 − k

], (18)

where k

′ = k/L0. Eq. (18) reveals that the swing amplitude increases every half-cycle

according to a function related to 1/(1 − k

). This reveals that the swing accumulates the net

energy from the child’s active motions in each pumping cycle. This net energy stems from the

work done by the child’s active force when standing up, which increases the height by k, over

the energy spent when squatting down, which decreases the height by kcosθn. It is worth

mentioning that Eq. (18) is obtained based on the neglect of the impact of standing squatting

motions. This contribution is −2l(̇ t)θ̇(t)/L(t) for θ̈(t) in Eq. (13), revealing that the standing

results in an increase for |θ̇(t)|. Therefore, the realistic increase of θn (shown in Fig. 4) should

be greater the prediction θn = arccos[1.11(cosθn−1 − 0.1)] by substituting parameters in the

numerical simulations into Eq. (18).

The Responsive Active Force for Pumping A Swing with Linear Friction

Next, we explore a more realistic scenario in which both active and frictional forces are at

play. A particularly noteworthy situation occurs when the responsive active force

counterbalances the frictional force, leading to stable oscillation with a constant amplitude

that neither decays nor expands. Such a state represents a stable equilibrium that is

sometimes observed in swing sports. An intriguing question is whether our active-force

model (Eq. (12) and (13)) can accurately simulate this condition.

Fig. 5: Active-motion simulations using Eqns. (12-16) showcasing a child pumping a swing in

the presence of finite friction, as shown by the solid red lines. To serve as comparisons, the

solid blue lines (indicating finite friction) and dashed black lines (representing no friction)

Page 14 of 19

177

Li, R., & Cui, W. (2024). Harnessing Active Force: The Pumping Mechanism of Child’s Swing Motion. European Journal of Applied Sciences, Vol -

12(4). 164-182.

URL: http://dx.doi.org/10.14738/aivp.124.17314

illustrate the simple pendulum motion of a stone with the same mass as the child. The

parameters used for these simulations are listed in Table II.

As shown in Fig. 5, the active-force model successfully replicates this scenario. Specifically, for

the stone without the active force, the swing amplitude demonstrated a decay (as shown by

the solid blue lines) when compared to the harmonic oscillations without friction

(represented by dashed black lines). In contrast, for a child exerting an appropriately strong

responsive active force (denoted by solid red lines), the swing amplitude remains constant (as

seen in images (a) to (c)). This essentially means that, in this situation, the energy pumped

from the responsive active force successfully counteracted the damping effect of friction.

Initially, it can be inferred that the frictional force is counterbalanced by the responsive active

force, implying that only the net active force minus the frictional force needs to be considered.

However, this was not the case. As is evident from Fig. 5, notable differences exist between the

balance of the active force and frictional contributions to the swing amplitude (solid red lines)

and the simple harmonic motion, where both forces perfectly nullify each other (dashed black

lines). These discrepancies are manifested in the smaller period of the former case (2.82 s) by

2% compared with the latter case (2.89 s), despite a less than 1/500 difference between their

amplitudes. This is intriguing, as a larger amplitude generally corresponds to a larger period

in a scenario devoid of an active force. Nevertheless, according to the simple relation T =

2π√L/g, the nontrivial smaller period for the child is brought about by the reduction in the

pendulum length owing to the standing squatting motions. The root cause of this is the

frictional force comprising both the radial and circumferential components, in contrast to the

active force, which is exclusively radial. This results in the impracticality of perfectly

counteracting the frictional force regardless of the form of the radial active force. The actual

scenario involves achieving an energy balance with the radial work executed by the active

force compensating for the energy loss induced by the circumferential component of the

frictional force.

Table II: The parameters selected for the swing simulations involving a stone (zero

active force) and a child (finite active force) under conditions of finite friction, as

shown in Fig. 5.

System Mass Maximum

length

Gravitational

acceleration

Friction

coefficient

Standing

height

Pulse

angle

Pulse

velocity

Initial

angle

Initial

velocity

M

(kg)

L0(m) g(kg. s

−2

) b(kg. s

−1

) k ca cb(s

−1

) θ(0) θ̇(0)

Stone 20 2 9.8 3.64 0 — — π/6 0

Child 20 2 9.8 3.64 0.2 0.12 0.20 π/6 0

We now turn to the primary parameters that determine the amplitude of the swing propelled

by the active force. Holding constant parameters such as the child's mass, swing length,

resistance, and initial conditions, we found that the child's center of mass elevation (the

height difference between the standing and squatting positions) significantly influences the

amplitude. For instance, Fig. 6(a) illustrates that when the standing amplitude surpasses 0.2

meters, the oscillation of the swing gradually increases (as indicated by the blue lines).

Conversely, the oscillation diminishes progressively when the amplitude drops below 0.2

Page 15 of 19

Services for Science and Education – United Kingdom 178

European Journal of Applied Sciences (EJAS) Vol. 12, Issue 4, August-2024

meters (indicated by dashed black lines). On the other hand, when the difference in the center

of mass height between standing and squatting is fixed at 0.2 meters for each swing (Fig. 6f),

the speed of standing (ca

) and squatting (cb) also affects the amplitude (Fig. 6d). The faster

the standing and squatting motions are, the larger the magnitudes are. Therefore, beyond the

typical factors influencing both animate and inanimate systems, such as mass, swing length,

resistance, and initial conditions, the pivotal determinant of the amplitude in a swing

propelled by standing is the difference in the center of mass height between standing and

squatting and the standing and squatting speeds.

Fig. 6: The amplitude alterations attributable to height (k) variation ((a)-(c)) or speed (ca and

cb) changes in the standing-squatting motion ((d)-(f)). The adjusted parameters are denoted in

legends. Other parameters align with those specified for active motions in Table II.

DISCUSSION AND IMPLICATION

This paper introduces a compelling argument for the existence and necessity of the 'active

force' concept to elucidate the dynamics of living objects in the living state, using the human- pumping swing action as an example. This active force, originating from the interactions

among the body, mind, and environment, provides a unique contribution to the dynamics of

living systems, a facet that conventional physics often disregards. We established a

comprehensive mechanical framework applicable to living and nonliving systems by

incorporating an active force into Newton's second law. This innovative governing equation

was applied to describe the swing motions of a child and an equally weighted stone, focusing

on their differences. Our study reveals that children with active force can sustain or augment

their amplitude despite friction, whereas a stone's oscillation can only decrease. Quantitative

analysis indicated that the energy pumping caused by the responsive active force (i.e., the

total active force of the body) performing work in each standing motion was responsible for

this phenomenon.

Furthermore, we identified that the responsive active force exhibits a pulse-like pattern,

whereas a linear style (e.g., l = −kθ) fails to generate a self-excited oscillation. Therefore,

Page 16 of 19

179

Li, R., & Cui, W. (2024). Harnessing Active Force: The Pumping Mechanism of Child’s Swing Motion. European Journal of Applied Sciences, Vol -

12(4). 164-182.

URL: http://dx.doi.org/10.14738/aivp.124.17314

beyond the typical factors influencing both animate and inanimate systems, such as mass,

swing length, resistance, and initial conditions, the pivotal determinant of the amplitude in a

swing propelled by standing is the difference in the center of mass height between standing

and squatting and the standing and squatting speeds. These findings underscore the existence

and necessity of the 'active force' concept for understanding living system dynamics, offering

a paradigm and mechanical framework for further exploration into life mechanics [16].

However, this research constitutes a preliminary study of the global (responsive) active force.

Future research should first probe further into the quantitative measurements and

calculations of both internal (i.e., local) and responsive active forces in the self-determined

motions of living beings, such as development, metabolism, and sports in plants, animals, and

humans. Such efforts may reveal novel patterns and mechanisms of both active forces as well

as their critical quantitative relations, laying a scientific foundation for predicting and

controlling life movements. Furthermore, although the current model prioritizes the active

force to emphasize its significance, it does not neglect the effects of swing constraints but can

address the impacts of both body and environmental constraints. More importantly, by

studying the quantitative mechanical relation between the internal and the responsive active

forces in future research, we can clarify the physical mechanism of the environmental

constraints or, in other words, the body-environment interaction.

It is crucial to remember that the active force discussed herein represents the summation of

all the active forces experienced by the human body's center of mass. Actual measurements

might necessitate measuring the contact at multiple points between the human body and the

interacting object, such as the contact of the feet and hands with a swing. By vectorially

synthesizing the forces at multiple points, we can obtain the resultant force at the center of

mass, as discussed in this paper. Consequently, further theoretical development should

consider the movement of multiple body parts under forces acting at various points on the

human body via Eq. (1). In this context, an immediate question would be to investigate the

active force pattern in 'pumping a swing from a seated position’ and compare it with the

results of the present study. This exploration would necessitate considering three subsystems

of the human body: the torso, thighs, and lower legs [25,31].

Particularly noteworthy is that the active force is a pivotal control mechanism of the mind

over the body during human motion. Optimal movement control is often characterized by the

timeliness, strength, and controllability of the active force in response to the mind. Therefore,

the practice and measurement of the active force may be a significant topic in the field of

sports training and rehabilitation therapy. In this regard, the relationships between active

force, bioelectricity, and consciousness present an intriguing topic. The active forces shown in

Figs. (4)–(6) exhibit a pulsating characteristic in the time series, reminiscent of the pulsation

patterns of bioelectric signals such as ECG and EEG [39]. We hypothesized that this similarity

is not coincidental, suggesting that active force indeed embodies the characteristics of life.

This is because the active force pattern in the pump swing is a consequence of an individual's

conscious decision in their movement mode, which is a product of the brain and heart's

electrical activities. In future studies, we will propose simultaneous measurements and

mathematical modeling of active force with EEG and ECG signals to investigate their

Page 17 of 19

Services for Science and Education – United Kingdom 180

European Journal of Applied Sciences (EJAS) Vol. 12, Issue 4, August-2024

quantitative correlations, potentially advancing our understanding of the underlying physical

mechanisms connecting active force, bioelectricity, and human conscious movement.

ACKNOWLEDGMENT

This research was funded by the National Key Research and Development Program of China

(2022YFC2805200), start-up funding from Westlake University (041030150118), and the

Scientific Research Funding Project of Westlake University (2021WUFP017). During the

preparation of this work the authors used the GPT-4 model in order to do language editing.

After using this tool, the authors reviewed and edited the content as needed and take full

responsibility for the content of the publication.

Data Access Statement

All relevant data are within the paper.

Conflict of Interest Declaration

The authors have declared that no competing interests exist.

References

1. Dyson, F., Our biotech future. The New York Review of Books, 2007. 54: p. 12.

2. Lynn, M., Carl, S., & Dorion, S. (2023). Life. Retrieved April 6, 2023, from

https://www.britannica.com/science/life.

3. Kennedy, D. and C. Norman, What Don't We Know? Science, 2005. 309(5731): p. 75-75.

4. Bianconi, G., et al., Complex systems in the spotlight: next steps after the 2021 Nobel Prize in Physics. J. Phys.

Complexity, 2023. 4(1): p. 010201.

5. Schrödinger, E., What is life?: With mind and matter and autobiographical sketches2012: Cambridge

University Press.

6. Allen, G., Life sciences in the twentieth century. J. Hist. Biol., 1976. 9(2).

7. Allen, G.E., Mechanism, vitalism and organicism in late nineteenth and twentieth-century biology: the

importance of historical context. Stud. Hist. Phi. Part C, 2005. 36(2): p. 261-283.

8. Von Bertalanffy, L., The history and status of general systems theory. Acad. Manage. J., 1972. 15(4): p. 407-

426.

9. Driesch, H., Psychical research: The science of the super-normal1933: Ayer Publishing.

10. Von Foerster, H. and G.W. Zopf. Principles of self-organization. in University of Illinois Symposium on Self- Organization,(1961: Robert Allerton Park). 1962. Pergamon Press.

11. Haken, H., Synergetics: Introduction and Advanced topics2004, Berlin: Springer

12. Bertalanffy, L.v., General system theory: Foundations, development, applications1968: G. Braziller.

13. Royama, T., Analytical population dynamics1992, London: Chapman & Hall.

14. Castellani, B and Gerrits, L . Map of the complexity sciences. Art and Science Factory, LLC. (2021).

Page 18 of 19

181

Li, R., & Cui, W. (2024). Harnessing Active Force: The Pumping Mechanism of Child’s Swing Motion. European Journal of Applied Sciences, Vol -

12(4). 164-182.

URL: http://dx.doi.org/10.14738/aivp.124.17314

15. Kelso, J.A.S., On the coordination dynamics of (animate) moving bodies. Journal of Physics: Complexity, 2022.

3(3): p. 031001.

16. Yang, W., P. Zhao, and W. H.T., An overview of mechanics (in Chinese)2020, Beijing: Science Press

17. Gompper, G., et al., The 2020 motile active matter roadmap. J. Phys.: Condens. Matter 2020. 32(19): p.

193001.

18. Ahmed, W.W., É. Fodor, and T. Betz, Active cell mechanics: Measurement and theory. BBA - Mol. Cell Res.,

2015. 1853(11, Part B): p. 3083-3094.

19. HILL, A.V., The Mechanism of the Nervous System. Nature, 1928. 123(3088): p. 9-11.

20. Rassier, D.E., B. MacIntosh, and W. Herzog, Length dependence of active force production in skeletal muscle. J.

Appl. Physiol. , 1999. 86(5): p. 1445-1457.

21. Weiss, P.L., R.E. Kearney, and I.W. Hunter, Position dependence of ankle joint dynamics—II. Active mechanics.

J. Biomechanics, 1986. 19(9): p. 737-751.

22. W. C. Cui, On an axiomatic foundation for a theory of everything. Philos. Study, 2021. 11(4): p. 241-267.

23. Weicheng, C., On the philosophical ontology for a general system theory. Philos. Study, 2021. 11(6): p. 443-

458.

24. Cui, W.C., R. Li, and L.L. Pan, A comparison of new general system theory philosophy with Einstein and Bohr.

Philos. Study, 2023. 13: p. 1-22.

25. Weicheng, C., On the trajectory prediction of a throwing object using new general system theory. Philos. Study,

2022. 12(2): p. 53-64.

26. Pan, L. and W. Cui, Re-examination of the two-body problem using our new general system theory. Philos.

Study, 2021. 11(12): p. 891-913.

27. Yuke, H. and C. Weicheng, Effect of the Earth Movement on the Measured Moon Trajectory. Philos. Study,

2022. 12: p. 641-680.

28. Goldstein, H., C. Poole, and J. Safko, Classical mechanics: 3rd2002: Pearson Education

29. Klimina, L. and A. Formalskii, Three-link mechanism as a model of a person on a swing. J. Comput. Syst. Sci.

Int., 2020. 59: p. 728-744.

30. Onyshko, S. and D. Winter, A mathematical model for the dynamics of human locomotion. J. Biomech., 1980.

13(4): p. 361-368.

31. Hanavan, E.P., A mathematical model of the human body. Dayton, OH: Aerospace Medical Division, Wright

Patterson Air Force Base, 1964: p. 64-102.

32. Gore, B.F., The Child's Swing. Am. J. Phys., 1970. 38(3): p. 378-379.

33. Curry, S.M., How children swing. Am. J. Phys., 1976. 44(10): p. 924-926.

34. Case, W.B., The pumping of a swing from the standing position. Am. J. Phys., 1996. 64(3): p. 215-220.

35. Bae, S., Equivalence of the pumping of a swing and the parametric resonance. Eur. J. Phys., 2006. 27(2): p.

Page 19 of 19

Services for Science and Education – United Kingdom 182

European Journal of Applied Sciences (EJAS) Vol. 12, Issue 4, August-2024

291.

36. Glendinning, P., Adaptive resonance and pumping a swing. Eur. J. Phys., 2020. 41(2): p. 025006.

37. Hirata, C., et al., Initial phase and frequency modulations of pumping a playground swing. Phys. Rev. E, 2023.

107(4): p. 044203.

38. Wirkus, S., R. Rand, and A. Ruina, How to pump a swing. Coll. Math. J., 1998. 29(4): p. 266-275.

39. Malmivuo, J. and R. Plonsey, Bioelectromagnetism: principles and applications of bioelectric and biomagnetic

fields1995: Oxford University Press.