Critical characteristics and the irreducible knee joint
by Stuart Burgess
Summary
Opponents of Neo-Darwinian evolution have argued that it is impossible, because
many biological systems require an irreducible number of parts for the system to
have any useful function. The concept of irreducibility requires a set of characteristics
that must exist simultaneously. Such characteristics are termed critical characteristics.
The advantage of identifying critical characteristics is that they give an indication
of the minimum quantity of design information that must exist simultaneously in
the genetic code for a mechanism to have any useful function. The irreducible mechanism
of the knee joint is shown to contain at least 16 critical characteristics, each
requiring thousands of precise units of information to exist simultaneously in the
genetic code. This demonstrates that the knee could not have evolved but must have
been created as a fully functioning limb joint from the beginning of its existence.
Introduction
According to the theory of evolution, natural mechanisms such as limb joints have
evolved one characteristic at a time by random and rare genetic mistakes, called
mutations. Evolutionists admit that mutations generally give rise to disability
and suffering, because organisms are so delicately balanced that random changes
tend to cause all kinds of malfunctions. For example, mutations are known to be
responsible for serious genetic disorders such as hemophilia and cystic fibrosis.1 However, despite the damaging nature
of mutations, evolutionists believe that sometimes there are mutations that produce
an improvement in the functioning of an organism. Evolutionists believe that these
‘favourable mistakes’ are inherited by offspring and accumulate so that
a new species evolves. Evolution is believed despite a complete absence of indisputable
evidence for the existence of any information-adding mutations.2
Definition of an irreducible mechanism
Evolution is based on a key assumption that natural mechanisms within organisms
can evolve incrementally so that all intermediate mechanisms
have some useful function that gives a survival advantage. A mechanism that can
evolve one characteristic at a time whilst always having a useful function can be
called a reducible mechanism. A mechanism that cannot evolve one
characteristic at a time whilst always having a useful function can be called an
irreducible mechanism. Behe has recently applied the term irreducible to
biochemical systems that cannot evolve.3
However, opponents of evolution have used the basic concept of irreducibility for
a long time. For example, the argument that bird flight requires ‘many parts
to be simultaneously present’ has been used for many years.4
Even Darwin himself admitted that evolution could only produce a reducible mechanism.
In his Origin of Species, Darwin says:
‘If it could be demonstrated that any complex organ existed which could not
possibly have been formed by numerous, successive, slight modifications, my theory
would absolutely break down.’ 5
One of the most vocal evolutionists of our day, Richard Dawkins, is also adamant
that evolution can only work if it is incremental.6
Since an intelligent designer is not restricted to incremental change, he is able
to create irreducible mechanisms without any difficulty. This means that an intelligent
designer has an inherently far greater capacity for ingenious design than does the
process of evolution. It is interesting to note that evolutionists sometimes admit
that the process of evolution is very restricted compared to intelligent design
because of the constraint of incremental change. For example, Steven Vogel says:
‘… the evolutionary process faces constraints far more severe than
anything impeding human designers. We biologists recognise these constraints, but
we don’t often rise above our natural chauvinism and make enough noise about
them. Every organism must grow from an initially smaller to an ultimately larger
size. Nature in effect must transmute a motorcycle into an automobile while providing
continuous transportation. The need for growth without loss of function can impose
severe geometrical limitations.’ 7
It is important to note the confession that biologists do not make enough noise
about the constraints of evolution because there is an obvious contradiction between
the enormous restrictions of evolution and the obvious superiority of design in
the natural world!
Since only intelligent design can produce an irreducible mechanism, the existence
of irreducible mechanisms in nature demonstrates the existence of an intelligent
Designer.8 Identifying irreducible
mechanisms in nature is very important, because evolutionists are very clever at
focusing attention on non-essential parts within mechanisms. For example, Dawkins
places much attention on how the lens in the human eye is not essential to the basic
functioning of the eye and how this supposedly supports the theory of evolution.9
Definition of a critical characteristic
In this paper, the concept of irreducibility is developed further to the level of
an irreducible set of characteristics that must exist simultaneously for a mechanism
to have any useful function. Such characteristics are termed critical characteristics.
Critical characteristics must not only be simultaneously present, but they must
also be simultaneously and precisely compatible with each other in order to produce
the required physical effects. In general, the critical characteristics of mechanical
mechanisms are often geometrical characteristics, because these must have precise
values whereas other characteristics such as material properties do not usually
have to have precise values. The advantage of identifying an irreducible set of
critical characteristics is that they give an indication of the minimum quantity
of information in the genetic code that must exist simultaneously and correctly.
The identification of a set of critical characteristics provides overwhelming evidence
that a natural mechanism could not have evolved.
The irreducible human knee joint
Figure 1. Anatomy of the knee joint (peripheral ligaments and knee
cap removed). F = Femur, T = Tibia, LC = Lateral condyle, MC = Medial condyle, PCL
= Posterior cruciate ligament, ACL = Anterior cruciate ligament.
There are basically three types of limb joint in animals and humans. These are the
ball and socket joint (e.g. hip and shoulder), the pivot joint (e.g. elbow) and
the condylar joint (e.g. knee). The knee joint is the largest and most complex joint
in the human body. The knee is called a condylar joint because of the articulation
between the femur and the tibia, as shown in Figures 1 and 2.10 The femur has two protrusions called condyles. These
have a convex curvature in order to roll and slide against the tibia. The tibia
has two concave grooves that match the condyles of the femur. The two central ligaments
that connect the tibia to the femur are called cruciate ligaments because
of the way they form a cross. These cruciate ligaments fit neatly inside the space
between the two condyles.
The knee joint is an irreducible joint because each of its four complex parts needs
to exist simultaneously and in a complex assembly to be able to perform its basic
function. The two bones are essential because they perform the rolling and sliding
motion. The two cruciate ligaments are essential because they act as mechanical
linkages and perform a vital guiding function in the joint, as shown in Figure 2.
If just one ligament is removed, then the joint cannot function as a hinge, and
the joint can have no useful function.
Critical characteristics in the knee joint
Figure 2. The irreducible mechanism of the knee (bones cut away
to show cruciate ligaments).
The irreducibility of the knee joint is most clearly demonstrated by identifying
the critical geometrical characteristics that must be defined in the genetic code.
The knee has many critical geometrical characteristics because the two cruciate
ligaments and the two leg bones form a very sophisticated and precise mechanism,
called a four-bar hinge.11
The four-bar hinge mechanism of the knee is shown at various stages of rotation
in Figure 2. These stages of rotation are schematically presented in Figure 3 to
show clearly how the four-bar hinge works. The cruciate ligaments form the two crossed
bars (b & c) whilst the upper and lower bones effectively form the other two
bars (a & d). The cruciate ligaments are able to pivot where they are attached
to the bones (points 1, 2, 3 & 4) because they are made of a non-rigid material.
In a four-bar hinge, the length of each of the four bars remains constant, but the
angle between each bar can change so the lower leg can rotate. One important feature
of the four-bar hinge is that the instantaneous centre of rotation approximately
coincides with the cross-over point of the cruciate ligaments. This cross-over point
moves as the joint opens and closes so that the knee does not have a fixed point
of rotation, as does a simple pivot joint. The knee joint is a particularly sophisticated
kind of four-bar hinge, because the cruciate ligaments are not rigid and have to
be kept taut by the rolling action of the bones.
|
Part
|
Critical characteristics
|
No. of critical characteristics
|
|
Femur bone
|
Protrusion of two condyles
|
2
|
|
Convex curvature of two condyles
|
2
|
|
Position of ligament attachment points
|
2
|
|
Tibia bone
|
Concave curvatures of two tracks
|
2
|
|
Position of ligament attachment points
|
2
|
|
Anterior cruciate ligament
|
Position of ligament attachment points
|
2
|
|
Length of ligament
|
1
|
|
Posterior cruciate ligament
|
Position of ligament attachment points
|
2
|
|
Length of ligament
|
1
|
|
Total
|
|
16
|
|
Table 1: Critical characteristics in the knee joint.
|
There are at least 16 critical characteristics in the knee joint as shown in Table
1. These are geometrical characteristics that are absolutely essential to the joint.
For simplicity, these will be specified by the order of 16 genes in the genetic
code. It could be argued that the knee joint also requires characteristics to trigger
the growth of the four separate components. However, these have not been
included in Table 1 because the evolutionist may argue that the four components
already happened to exist in some ‘primitive joint’. It could also be
argued that the knee joint requires characteristics to describe a muscle actuator.
However, these too have been left out because the evolutionist may argue that these
already happened to exist in some ‘primitive joint’. Therefore, these
16 characteristics represent a conservative estimate of the minimum required critical
characteristics in the knee joint.
If any one of the critical characteristics shown in Table 1 is missing, then the
knee cannot function at all. Anyone who has experienced a ruptured cruciate ligament
will know this only too well. The 16 critical characteristics must not only be present,
but must also be precisely compatible with each other to produce the right physical
motion. The two bones must have a compatible curvature at their interface and this
curvature must also be precisely compatible with the position and movement of the
cruciate ligaments. In particular, the bones must be shaped so as to make the lower
leg rotate around the instantaneous centre of rotation of the four-bar hinge. If
the attachment points are not in the right place on the bones, then the instantaneous
centre of rotation of the knee joint will not be compatible with the shapes of the
bones, and the knee will seize up or fall apart. The ligaments must also be assembled
to the correct attachment points so that the ligaments form a cross as shown in
Figures 2 and 3. If one of the ligaments was assembled to the wrong attachment point
such that the cross was not formed, then the knee could not function as a hinge
and would be useless.
Figure 3. Schematic diagram of the four-bar mechanism in the knee
joint. See text for explanation.
Since a human characteristic is typically specified by one gene with about 1,000
chemical units of information, it requires many thousands of units of information
in the genetic code to specify the essential design information of the four-bar
hinge. The theory of evolution proposes that mutations cause random changes to units
of information in the genetic code and that this leads to evolution. Yet with the
knee, many thousands of precise units of information must be in place simultaneously
for the knee to have any usefulness.
Not only must all critical characteristics be present from the start but they must
also remain unchanged, otherwise this will cause the physical system to break down.
In the case of a healthy knee joint, if a random change is made to one of the critical
characteristics, such as the position of a ligament, then the knee will cease to
function properly because the position of the ligament is no longer compatible with
other critical characteristics. This shows why random gene mutations generally cause
malfunctions and suffering in living organisms.
The impossibility of an evolved knee
The knee joint presents a major challenge to the evolutionist because it is unique,
and because there are no intermediate forms of joint between a condylar joint and
the other two limb joints found in animals and humans—the ball and socket
joint and the pivot joint. The knee is widely acknowledged by anatomists as being
a completely distinct type of joint.12
This is because the knee uses completely different mechanical principles for hinged
movement. Whereas the knee has two mechanical linkages that perform a vital guidance
role (the cruciate ligaments), the joints of the hip, shoulder and elbow have no
such mechanical linkages at all. Whereas the knee rolls and slides, the joints of
the hip, shoulder and elbow only slide. Whereas the knee has a centre of rotation
that moves by up to several centimetres, the joints of the hip, shoulder and elbow
have a fixed centre of rotation.
It is interesting to note that some biology books describe the knee joint as a ‘highly
modified hinge joint’ implying that the knee must have evolved from
the simple pivot joint that exists in the elbow.10 The use of the term
‘highly modified’ shows that evolutionists are aware that there
is a big difference between a pivot joint and a condylar joint. In fact, the difference
is enormous because there are no known intermediate mechanisms between a simple
pivot hinge and a four-bar mechanism. Indeed, a pivot hinge has none of the critical
characteristics shown in Table 1. In particular, a pivot joint has nothing remotely
like the two crossed cruciate ligaments at the centre of the joint. The evolutionist
might argue that there is a similarity with the curved surfaces of the bones. However,
there is even a distinct difference in the curvature of the bones between the knee
and elbow joints because of the complex motion of the knee.
It would seem impossible for evolutionism to explain how an evolutionary process
could cause two ligaments to suddenly become crossed at the centre of a pivot joint,
precisely at the same time that a space is formed to accommodate them, and precisely
at the same time that a complex and compatible rolling motion is formed! The popular
evolutionist Dawkins claims that he is not aware of any type of complex organ that
could not have evolved by ‘numerous successive slight modifications’.13 However, the knee joint appears to
be one clear example of a mechanism within the human body that could not possibly
have evolved by numerous successive slight modifications.
Non-essential parts in the knee joint
The anatomy of the knee in Figure 3 is deliberately simplified in order to identify
the parts that are absolutely essential to the most basic function of the knee.
Having demonstrated that there is an irreducible mechanism within the knee that
cannot evolve, it is important to note that the complete knee contains an extremely
efficient and elegant design with many complex parts. These include a bone at the
front of the knee called the patella (knee-cap) and a fibrous capsule containing
several ligaments, which encloses and supports the joint. There is also a soft cartilage
to reduce shock loads between the bones and an elaborate arrangement of muscle fibres
connected to the front and back of the leg to enable the movement of the joint to
be finely controlled. There is even a lubricating fluid, called synovial fluid,
inside the knee that makes the joint rotate smoothly and last a long time.
The biomechanics of the knee are also simplified in Figure 3 for clarity. In reality,
the ligaments do stretch by a tiny amount when the knee is in certain positions.
There is also a small amount of torsional freedom between the femur and tibia. These
features make the knee joint an extremely sophisticated mechanism. Indeed, the knee
joint is so sophisticated that human designers have been unable to produce an artificial
knee that has anything approaching the performance of a real knee.
Even though the fine details of the knee joint give wonderful evidence of design,
it is only the irreducibility of the knee mechanism that can ‘prove’
the theory of evolution to be impossible. Evolutionists such as Richard Dawkins
are experts at focusing attention on non-critical parts. If evolutionists attempted
to discuss the evolution of the knee, I suspect they would describe in detail how
the knee-cap was not actually essential and how it just appeared and was retained
because it gave advantages. It is most likely that they would also say that the
lubricating fluid was not essential but that it suddenly appeared and remained because
it gave advantages. After giving many such examples, they may lead the reader into
thinking that every single part of the knee could just evolve by chance. It is therefore
very important to present to evolutionists the irreducible mechanism at the core
of the knee joint and to identify critical characteristics.
Non-critical characteristics in the knee joint
Non-critical characteristics are characteristics that do not have to be
simultaneously present with exact values for a system to perform a useful function.
Examples of non-critical characteristics in the knee joint include the colours and
material properties of the cruciate ligaments and bones. Since these characteristics
do not interact precisely with other characteristics and they do not affect the
basic functioning of the knee, it is theoretically possible for these non-critical
characteristics to evolve by mutation and in isolation. However, even though the
ligaments and bones could in theory change in terms of colour and material properties
by random mutations, these changes would not convert the knee into another kind
of mechanism!
The fact that evolution can in theory evolve characteristics that are non-critical
is used by the evolutionist to give the impression that evolution can work. School
textbooks often give examples of how a new colour of a creature such as a moth could
evolve by mutation, and then say that with many mutations the moth could have evolved
from a primitive creature. However, even though the colour of a moth may be important
to its survival, the characteristic of colour is nevertheless a trivial one in terms
of how it affects the functioning of organs and parts within the moth.
Therefore, the example of the evolution of colour by mutation is not an example
of evolution at all because no matter how many non-critical characteristics are
evolved, they can never change one kind of functioning system into another kind
of functioning system.
When discussing evolution, biology books will rarely distinguish between critical
and non-critical characteristics in an organism although characteristics are known
to vary greatly in importance. This is very surprising, because a characteristic
like the attachment position of a ligament is vastly more important than the colour
of the ligament. There is no doubt that critical characteristics are obscured because
evolutionists can only attempt to give trivial examples of evolution such as changes
in colour. To demonstrate the theory of evolution, the evolutionist would have to
show how a critical characteristic like the attachment position of the cruciate
ligaments could evolve. However, this has never been done and can never be done
because such a critical characteristic could not evolve in isolation.
Four-bar hinges in engineering
Four-bar hinges are commonly found in vehicle steering mechanisms. Engineers always
start the design exercise with a complete set of parts. Following on from the transport
analogy of Steven Vogel, the theory of evolution is analogous to proposing that
one can take the engineering drawings of a simple pivot joint used in a motorbike
steering wheel and evolve them into the drawings of the steering system of a four-wheeled
vehicle. The information on the drawings is equivalent to the genetic code, and
random photocopying errors in the information are analogous to mutations. The evolutionist
believes that the random photocopying errors will sometimes produce a slightly better
system, and that via selection, eventually the steering system of the motorbike
will turn into a four-bar hinge and form the steering system of a four-wheeled vehicle!
Such reasoning is absurd for several reasons. Firstly, if a random change were made
to the information on a drawing of a motorbike steering system, then this would
at best cause no change in the basic functions and at worst have catastrophic consequences.
Secondly, there are no intermediate mechanisms between a motorbike steering system
and a car steering system, whereas evolution would require hundreds of fully functioning
intermediate forms. In a similar way, it is impossible for the knee joint to have
evolved from a simple pivot joint such as the elbow joint.
The uniqueness of the human knee
The basic principle of the knee joint is unique whether it is the knee joint of
an animal or human being. However, there is yet a further problem for the evolutionist
in that the human knee is distinctly different from animal knees. In the case of
humans, the knee is designed to lock easily in extension (straight leg) so that
maintaining straight legs and a vertical posture is easy. This design feature is
one reason why man is a biped (two-legged) and is able to walk and run upright in
a completely natural way. Apes’ knees cannot lock and must be continually
loaded in flexion (bent leg). Thus apes are generally quadrupedal (four-legged)
and it is extremely difficult for apes to maintain a vertical posture with its legs.
Evolutionists admit that the only way apes can attempt to stand upright is by having
awkward bends at the ankle, knee and hip joints.14
Such a distorted posture means that apes can only stay vertical for short periods
and distances. In contrast, an able-bodied and fit human being can run many miles
without great difficulty!
Evolutionists admit that there is a key difference between the knees of animals
and humans. For example, Dye says:
‘Despite the overall similarity of the design of the knee in tetrapods, no
ideal animal model of the human knee is available.’ 15
That there are thousands of different types of animals on the earth that move with
a horizontal stature provides great evidence that humans have been deliberately
designed to be unique.
The power and wisdom of God
The human knee joint not only gives evidence of design but it also gives evidence
of the infinite power and wisdom of God. Solomon spoke of the wonder of growth in
the womb:
‘As you do not know what is the way of the wind, or how
the bones grow in the womb of her who is with child, so you do not know the works
of God who makes everything’ (Ecclesiastes 11:5).
Conclusion
Whether gene mutations are random (as atheists believe) or planned (as many theistic
evolutionists believe) the process of evolution cannot produce an irreducible mechanism
because evolution is restricted to incremental change in the genetic code.
The human knee joint is an irreducible mechanism that must have at least four complex
parts existing simultaneously and in a complex assembly to perform any useful function.
The 16 critical characteristics in the knee joint correspond to several thousand
units of information in the genetic code. These units of information cannot evolve
incrementally but must exist simultaneously for the knee to perform its basic function.
There are no intermediate forms of joint between the condylar joint of the knee
and the other two joints found in animals and humans—the ball and socket joint
and the pivot joint. And there are distinct differences between the knee joint of
animals and that of humans.
There is thus overwhelming evidence that the knee was created as a fully functioning
limb joint from the beginning of its existence.
Related articles
References
- Roberts, M.B.V., Biology a Functional Approach, 4th
Ed., Nelson, Walton-on-Thames, Surrey, p. 593, 1986. Return to text.
- Spetner, L, Not by Chance,
The Judaica Press, Brooklyn, New York, 1997. Return to text.
- Behe, M.J., Darwin’s
Black Box, Free Press, New York, p. 39, 1996. Return to text.
- For example, see Gish, D.T.,
Evolution: The Fossils Still Say NO! Creation-Life Publishers, El Cajon,
California, p. 88, 1972. Return to text.
- Darwin, C., (1872), Origin of Species, 6th Ed.,
New York University Press, New York, p. 154, 1988. Return to text.
- Dawkins, R., The Blind Watchmaker, Penguin, London, p.
49, 1986. Return to text.
- Vogel, S., Cats’ Paws and Catapults, Penguin, London,
p. 23, 1998. Return to text.
- Burgess, S.C., Hallmarks of Design, Day One Publications,
to be published January 2000. This book examines several irreducible mechanisms
in nature and also examines several other ‘hallmarks of design’.
Return to text.
- Dawkins, R., Ref. 6, pp. 80–81. Return to text.
- Segal, P. and Jacob, M., The Knee, Wolfe, London, p. 9,
1983. Return to text.
- O’Connor, J. and Goodfellow, J., The mechanics of the knee
and prosthesis design, Journal of Bone and Joint Surgery 60B:358–369,
1978. Return to text.
- Guyot, J., Atlas of Human Limb Joints, Springer-Verlag,
New York, p. 20, 1981. Return to text.
- Dawkins, Ref. 6, p. 91. Return to text.
- Hinchliffe, J.R. and Johnson, D.R., The Development of the
Vertebrate Limb, Clarendon Press, Oxford, pp. 37–39, 1980.
Return to text.
- Scott, F. and Dye, M.D., An evolutionary perspective of the knee,
Journal of Bone and Joint Surgery 69A:976–983, 1987.
Return to text.
| It has been said that “Information is power”. When it comes to creation information we’d have to agree. Keep the ‘powerful’ evidence for God being Creator coming.  | | |
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