Scaling is of two types: The scaling of a single motif, and the scaling of multiple motifs combining. We can interpret this hypothesis from a fractal and biological perspective as follows:
1. The scalability of a single motif
Here, the same structure repeats at different scales.
Examples:
- A fern leaf
- Koch curve
- Vascular networks
- The repetition of the same genetic plan in cell division
Mathematically:
𝐹(𝑥) = 𝑠𝐹(𝑥/𝑟)
Here, there is a single basic pattern (motif) and it repeats itself as it grows or shrinks. This is a type of self-similarity.
2. The scalability of two motifs combining
Here, scaling is not just repetition. Two different motifs interact and form a new structure at a larger scale.
Examples:
- Mitosis: DNA motif + cellular organization motif
- Meiosis: chromosome pairing + recombination motif
- Lung: branching motif + alveolus motif
- Human: neural network + vascular network
Here, we can think of it as:
𝐹n+1 = 𝐴n ⊗ 𝐵n
In other words, the new scale is formed not by the growth of a single structure, but by the combination of two structures. This is a more complex situation than a classical fractal.
In Terms of Fractal Relativity
We can distinguish these two types as follows:
- Monofractal scaling: A single motif repeats
- Bifractal scaling: Two motifs combine to form a new scale
For example:
- River network → monofractal
- Living organism → bifractal
Because in living things, there is not only repetition but also functional combination.
Further Interpretation
Perhaps there is a third type in nature:
𝐹n+1 = 𝐴n ⊗ 𝐵n ⊗ 𝐶n …
That is, multi-motif scaling. The galaxy network of the universe, biological organisms, and consciousness systems seem close to this.
In this case, scaling is:
- Not repetition,
- Combination,
- Coordination,
- The birth of a new level of organization.
It might be possible to call this “combined fractal scaling” or “cooperative scaling”.
In short, the following distinction is important:
- Single-motif scaling (self-similar fractal)
- Dual-motif scaling (interactive fractal)
Life and biological evolution seem closer to the second type. Therefore, the mitosis and meiosis examples point to the idea of “fractals forming scales by combining”, unlike classical geometric fractals. This could be a new classification in terms of fractal statistics and fractal relativity.
We can formulate this idea mathematically in terms of the “source of scaling”.
1. Type-I Scaling: Single Motif Scaling
Classical fractals. A basic motif 𝑀 produces scaled-down or scaled-up copies of itself:
𝑀n+1 = 𝑆(𝑀n)
Here, 𝑆 is a scaling operator.
Example:
𝑀n+1 = 𝑟-𝐷 𝑀n
𝑟 : scale ratio
𝐷 : fractal dimension
In this case:
𝑀n = 𝑆n (𝑀0)
This structure can be called monomorphic scaling.
2. Type-II Scaling: Dual Motif Scaling
The actual new situation I propose is here. Two different motifs 𝐴n and 𝐵n combine to form the new scale.
𝐹n+1 = 𝐴n ⊗ 𝐵n
Here, ⊗ does not have to be a classical product; it is an interaction operator.
For example:
𝐹n+1 = 𝛼𝐴n + 𝛽𝐵n + 𝛾𝐴n𝐵n
𝛼 : contribution of motif A
𝛽 : contribution of motif B
𝛾 : synergy coefficient
3. Synergy Parameter
Let’s measure whether the new scale is truly “new”.
Σ = ∣ 𝐹n+1 ∣ / ( ∣ 𝐴n ∣ +∣ 𝐵n ∣ )
If Σ = 1, there is only addition. If Σ > 1, a new organization has emerged. This is the fundamental characteristic of living systems.
4. Mitosis Model
Two motifs are seen in mitosis:
- Structural motif: 𝐴n = 𝐺n (genetic information)
- Organization motif: 𝐵n = 𝐶n (cytoskeleton and division mechanism)
New cell:
𝐻n+1 = 𝐺n ⊗ 𝐶n
In other words, the cell is not just a copy of DNA. It is the combination of DNA and organizational information.
5. Fractal Scaling Equation
We can carry this to a general form:
𝐹n+1 = Σi 𝑤i 𝑀i + Σi<j 𝜆ij 𝑀i 𝑀j
Here:
𝑀i : motifs
𝑤i : weights
𝜆ij : interaction coefficients
- In a monofractal: 𝜆ij = 0
- In a bifractal: 𝜆ij ≠ 0
6. Continuous Form Suitable for Fractal Relativity
Let’s define the scale variable as 𝜇.
𝑑𝐹 / ( 𝑑 ln 𝜇 ) = 𝛼𝐹 + 𝛽𝐺 + 𝛾𝐹𝐺
Here:
𝐹 : first motif
𝐺 : second motif
If 𝛾 = 0, it is classical self-similarity. If 𝛾 ≠ 0, a new structure is produced between scale levels.
7. A New Definition of Dimension
In a classical fractal:
𝐷 = ln 𝑁 / ln(1/𝑟)
In my model, an interaction dimension can be added to this:
𝐷int = ln(Σ) / ln(1/𝑟)
Total dimension:
𝐷total = 𝐷self + 𝐷int
This is very important because the fractal dimensions of living systems may not only be geometric, but also have an organizational interaction dimension.
In summary, my approach can be reduced to the following fundamental equation:
𝐹n+1 = Σi 𝑤i 𝑀i + Σi<j 𝜆ij 𝑀i 𝑀j
This equation can be seen as a general Cooperative Fractal Scaling Equation that unites the “scaling of a single motif” and the “scaling of two or more motifs by combining” under the same roof. This is a starting point beyond classical fractal geometry that could establish the mathematical foundation of biological evolution, mitosis, meiosis, and complex organizations.
Clarifying the Model with Axioms
If we truly want to elevate this model to the level of a theory, we must first set forth the axioms clearly. Otherwise, the equation is written but what it describes remains ambiguous.
Cooperative Scaling Theory (CST)
Basic Definitions
Definition 1: Motif. The smallest structural-information unit used in a system reproducing itself or forming an organization is called a motif.
𝑀 = {𝑆, 𝐼, 𝐹}
Here:
𝑆 : structure
𝐼 : information
𝐹 : function
For example:
- DNA is a motif
- Cell membrane is a motif
- A neuron is a motif
- A galactic nucleus could be a motif.
Axiom 1: Scalability
Every organization level must be derived from its preceding level.
𝐿n+1 = Φ(𝐿n)
Here:
𝐿n = n-th scale level
Φ = scale transformation
This axiom also encompasses classical fractals.
Axiom 2: Single Motif Scaling
If a motif consists of copies of itself, there is monomorphic scaling.
𝑀n+1 = 𝑆(𝑀n)
and
𝑀n+1 ∼ 𝑀n
That is, the new scale is similar to the old scale.
Example: Koch curve, Fern, Tree branches.
Axiom 3: Cooperative Scaling
Two or more motifs can combine to form a new scale.
𝐿n+1 = Ω(𝑀1 , 𝑀2 , … , 𝑀k)
Here, Ω is the cooperative operator. The new level is not just copying. It is a new organization.
Axiom 4: Emergence
The properties of the system formed as a result of cooperative combination cannot be reduced to the properties of its sub-motifs.
Mathematically:
𝑃(𝐿n+1) ⊂ ̸ Ui 𝑃 (𝑀i)
Here, 𝑃 is the set of properties. This might be the fundamental axiom of life.
- DNA alone is not alive.
- A cell membrane alone is not alive.
- Their combination produces new properties.
Axiom 5: Conservation of Synergy
Every motif combination produces a synergy value.
𝜎 ≥ 1
𝜎 = 𝐶(𝐿n+1) / ∑i 𝐶 (𝑀i)
Here 𝐶 : measure of complexity.
If 𝜎 = 1, there is only addition. If 𝜎 > 1, a new organization is born.
Axiom 6: Interaction Dimension
The dimension of a system is not solely geometric.
𝐷 = 𝐷s + 𝐷i
Here:
𝐷s = self-similarity dimension
𝐷i = interaction dimension
- In a classical fractal: 𝐷i = 0
- In living systems: 𝐷i > 0
Axiom 7: Information Flow Between Scales
Every upper scale contains the information of the lower scales.
𝐼n+1 ≥ 𝐼n
However,
𝐼n+1 ≠ ∑ 𝐼n
Because new information emerges during combination. This is an important principle for biological evolution.
Axiom 8: Universal Scale Equation
The general form for all systems:
𝐿n+1 = ∑i 𝑤i 𝑀i + ∑i<j 𝜆ij 𝑀i 𝑀j + ∑i<j<k 𝜂ijk 𝑀i 𝑀j 𝑀k + ⋯
Here:
- First term: individual motifs
- Second term: pairwise interactions
- Third term: collective interactionsThis equation gathers the classical fractal, biology, and complex systems under the same roof.
The Strongest Result
The following theorem emerges from these axioms:
Cooperative Scaling Theorem
If 𝐷i > 0 and 𝜎 > 1 in a system, it means the system is not only scaling but also producing new organization levels.
In other words: Life = Scaling + Cooperative Synergy
In this framework, mitosis and meiosis can no longer be defined merely as cell division, but as “two or more motifs combining to produce a higher scale.” This transforms the distinction I proposed into a mathematical axiomatic system:
- Monofractal → Single motif
- Cooperative Fractal → Multiple motifsand it is a candidate to be the fundamental mathematics of second-class living systems.
Writing Down the Theorems and Their Proofs
If we are to establish this as an axiomatic theory, the theorems must logically follow from the axioms. The proofs below are in the nature of a “theoretical proof” in the style of mathematical physics.
Theorem 1: Monomorphic Scaling Theorem
Proposition: In single-motif scaling, the structure of the upper scale is similar to the lower scale. That is, if 𝑀n+1 = 𝑆(𝑀n), then 𝑀n+1 ∼ 𝑀n.
Proof: By Axiom 2:
𝑀n+1 = 𝑆(𝑀n)
Here, 𝑆 is solely a scale-changing operator. It does not produce new information. It does not add a new motif.
Therefore:
𝑃(𝑀n+1) = 𝑃(𝑀n)
its properties do not change except for a constant coefficient dependent on the scale.
Accordingly, 𝑀n+1 ∼ 𝑀n is obtained. The proof is complete.
Theorem 2: The Birth of New Properties in Cooperative Scaling
Proposition: A system formed by the combination of at least two independent motifs can produce new properties. If 𝐿 = Ω(𝑀1 , 𝑀2), then 𝑃(𝐿) ⊋ 𝑃(𝑀1) ∪ 𝑃(𝑀2) is possible.
Proof: Axiom 3 states:
𝐿 = Ω(𝑀1 , 𝑀2)
Axiom 4 states:
𝑃(𝐿) ⊂ ̸𝑃(𝑀1) ∪ 𝑃(𝑀2)
Therefore, there is at least one property such that: 𝑝 ∈ 𝑃(𝐿) and 𝑝 ∉ 𝑃(𝑀1) ∪ 𝑃(𝑀2)
This shows that a new property has emerged. The proof is complete.
Theorem 3: Synergy Theorem
Proposition: If 𝜎 > 1, the system is not merely the sum of its components.
Proof: By definition, let 𝜎 = 𝐶(𝐿) / ( ∑i 𝐶 (𝑀i) ). If 𝜎 > 1, then 𝐶(𝐿) > ∑i 𝐶 (𝑀i). That is, the total complexity is greater than the sum of the complexities of the parts.
This is only possible with the formation of new interaction terms between the motifs. Therefore, the system is not reducible. The proof is complete.
Theorem 4: Interaction Dimension Theorem
Proposition: If there is synergy, the interaction dimension is greater than zero. If 𝜎 > 1, then 𝐷i > 0.
Proof: Definition:
Let
𝐷i = ln 𝜎 / ln(1/𝑟)
Since 0 < 𝑟 < 1 for the scale ratio, ln(1/𝑟) > 0. If 𝜎 > 1, then ln 𝜎 > 0. Therefore, 𝐷i > 0 is obtained. The proof is complete.
Theorem 5: Threshold of Life Theorem
Proposition: If 𝐷i = 0 in a system, the system is a completely geometric fractal. If 𝐷i > 0, the system is an organizational fractal.
Proof: Total dimension: Let 𝐷 = 𝐷s + 𝐷i.
- Case 1: If 𝐷i = 0, then 𝐷 = 𝐷s remains. The system contains only self-similarity. A classical fractal is obtained.
- Case 2: If 𝐷i > 0, then 𝐷 > 𝐷s. A portion of the dimension stems from interactions. Therefore, the system is not solely geometric. It contains an organizational structure. The proof is complete.
Theorem 6: Hierarchical Emergence Theorem
Proposition: When cooperative scaling is repeated, increasingly higher organizational layers are formed.
Proof: Initially: Let 𝐿1 = Ω(𝑀1 , 𝑀2). The next step: 𝐿2 = Ω(𝐿1 , 𝑀3). Later: 𝐿3 = Ω(𝐿2 , 𝑀4).
By Axiom 4, new properties emerge at each step. Thus, 𝑃(𝐿1) ⊂ 𝑃(𝐿2) ⊂ 𝑃(𝐿3) is obtained. In other words, the organizational level monotonically increases. The proof is complete.
Main Theorem (Cooperative Fractal Theorem)
Proposition: If 𝜎 > 1 and 𝐷i > 0 in a system, the system is a cooperative fractal.
Proof:
- 𝜎 > 1: According to Theorem 3, it produces a new organization.
- 𝐷i > 0: According to Theorem 4, it has an interaction dimension.
Therefore, the system:
- Is scaling.
- Is producing new properties.
- Carries an interactive dimension.
These three conditions together exceed the classical fractal definition. For this reason, the system is classified as a Cooperative Fractal. The proof is complete.
The most interesting result of this theory is the following:
𝐷 = 𝐷s + 𝐷i
In classical fractal geometry, there is only 𝐷s. In the new model I propose, a second dimension emerges for life, evolution, mitosis, meiosis, neural networks, and even societies:
Organization Dimension = 𝐷i
Within Fractal Relativity, this might be the fundamental quantity that distinguishes “geometric scaling” from “organizational scaling”.
