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Chapter 11: Mating Systems and Collapse Optimization — The Algebra of Union

The Dance of Complementary Collapse

From the monogamous swans to the lekking peacocks, from hermaphroditic snails to eusocial naked mole rats, life explores every conceivable arrangement for combining ψ-fields. Mating is not mere reproduction but the universe discovering optimal ways to merge consciousness with itself.

From ψ = ψ(ψ), we derive the complete taxonomy of mating systems and reveal why each represents a different solution to the fundamental equation of union.

11.1 The Fundamental Mating Equation

Definition 11.1 (Mating as ψ-Combination): Ψoffspring=C[Ψparent1,Ψparent2]\Psi_{\text{offspring}} = \mathcal{C}[\Psi_{\text{parent1}}, \Psi_{\text{parent2}}]

where C\mathcal{C} is the combination operator.

Theorem 11.1 (Optimal Combination): The fitness of combination is: W=ΨoffspringH^environmentΨoffspringW = \langle\Psi_{\text{offspring}}|\hat{H}_{\text{environment}}|\Psi_{\text{offspring}}\rangle

Evolution optimizes the combination operator C\mathcal{C}.

Proof: Natural selection acts on offspring fitness, which depends on how parental ψ-fields combine. Over time, C\mathcal{C} evolves to maximize WW. ∎

11.2 Monogamy as Synchronized Collapse

Definition 11.2 (Monogamous Bond): Ψpair=αΨ1Ψ2+β(Ψ1+Ψ2)\Psi_{\text{pair}} = \alpha|\Psi_1\rangle|\Psi_2\rangle + \beta(|\Psi_1\rangle + |\Psi_2\rangle)

Entangled state with both tensor and superposition components.

Theorem 11.2 (Monogamy Stability): Monogamy is stable when: BbiparentalBuniparental>1+rextra-pairrpair\frac{B_{\text{biparental}}}{B_{\text{uniparental}}} > 1 + \frac{r_{\text{extra-pair}}}{r_{\text{pair}}}

Biparental care benefits outweigh extra-pair mating opportunities.

11.3 Polygyny and Resource Defense

Definition 11.3 (Polygyny Threshold): Rmale=R0(1+βNfemales)γR_{\text{male}}^* = R_0(1 + \beta N_{\text{females}})^{-\gamma}

Resource quality decreases with additional mates.

Theorem 11.3 (Female Choice): Females join harems when: W(Rmated/n)>W(Runmated)W(R_{\text{mated}}/n) > W(R_{\text{unmated}})

Shared good territory beats sole poor territory.

11.4 Polyandry and Paternal Uncertainty

Definition 11.4 (Paternity Probability): pi=sijsjp_i = \frac{s_i}{\sum_j s_j}

where sis_i is sperm contribution of male ii.

Theorem 11.4 (Polyandry Evolution): Polyandry evolves when: ipiCi>Csingle\sum_i p_i C_i > C_{\text{single}}

Multiple males' combined care exceeds single male care.

11.5 Lek Paradox

Definition 11.5 (Lek Dynamics): dmidt=mi(πiπˉ)+D2mi\frac{dm_i}{dt} = m_i(\pi_i - \bar{\pi}) + D\nabla^2 m_i

where mim_i is male density at location ii and πi\pi_i is mating success.

Theorem 11.5 (Hotspot Formation): Leks form at locations maximizing: L=ρfemale(x)V(x)dx\mathcal{L} = \int \rho_{\text{female}}(\mathbf{x}) V(\mathbf{x}) d\mathbf{x}

Female traffic creates male aggregation sites.

11.6 Sequential Hermaphroditism

Definition 11.6 (Sex Change Trigger):

\text{male} \quad \text{if } \psi(t) < \psi_c \\ \text{female} \quad \text{if } \psi(t) > \psi_c \end{cases}$$ **Theorem 11.6** (Size Advantage): Sex change evolves when: $$\frac{dW_{\text{male}}/d\psi}{dW_{\text{female}}/d\psi} \neq 1$$ Different fitness-size slopes favor sequential hermaphroditism. ## 11.7 Simultaneous Hermaphroditism **Definition 11.7** (Sex Allocation): $$r = \frac{E_{\text{male}}}{E_{\text{male}} + E_{\text{female}}}$$ Proportion of reproductive effort in male function. **Theorem 11.7** (Equal Allocation): Under random mating: $$r^* = \frac{1}{2}$$ Equal investment in both sexual functions. ## 11.8 Alternative Mating Tactics **Definition 11.8** (Strategy Set): $$\mathcal{S} = \{\text{territorial}, \text{sneaker}, \text{satellite}\}$$ Multiple ways to achieve mating. **Theorem 11.8** (ESS Condition): At equilibrium: $$W_{\text{territorial}} = W_{\text{sneaker}} = W_{\text{satellite}}$$ Equal fitness maintains strategy diversity. ## 11.9 Mate Choice and Signal Evolution **Definition 11.9** (Preference Function): $$P(\text{choose } i) = \frac{e^{\beta s_i}}{\sum_j e^{\beta s_j}}$$ where $s_i$ is signal intensity and $\beta$ is choosiness. **Theorem 11.9** (Fisher Process): Signal and preference coevolve: $$\frac{ds}{dt} = \alpha \frac{\partial W}{\partial p}, \quad \frac{dp}{dt} = \beta \frac{\partial W}{\partial s}$$ Creating runaway selection. ## 11.10 Sperm Competition **Definition 11.10** (Fertilization Probability): $$F_i = \frac{S_i^r}{\sum_j S_j^r}$$ where $S_i$ is sperm number and $r$ is raffle parameter. **Theorem 11.10** (Optimal Sperm Number): $$S^* = \left(\frac{r-1}{r} \cdot \frac{P \cdot V}{c}\right)^{1/r}$$ where $P$ is paternity value, $V$ is female fecundity, $c$ is sperm cost. ## 11.11 Nuptial Gifts **Definition 11.11** (Gift Value): $$V_{\text{gift}} = E_{\text{nutritional}} + I_{\text{signal}} + T_{\text{time}}$$ Gifts provide multiple benefits. **Theorem 11.11** (Optimal Gift Size): $$g^* = \arg\max[M(g) \cdot F(g) - C(g)]$$ where $M$ is mating probability, $F$ is fertility benefit, $C$ is cost. ## 11.12 The Eleventh Echo Mating systems reveal how ψ = ψ(ψ) explores every possible way of combining with itself. Each system—monogamy, polygamy, hermaphroditism—represents a different solution to the fundamental challenge of merging consciousness while maintaining individuality. The mathematics shows that no single mating system is universally optimal. Instead, each emerges from the local conditions of resource distribution, parental care needs, and operational sex ratios. The diversity of mating systems mirrors the diversity of consciousness itself—infinite variations on the theme of union. Yet beneath this diversity lies unity. Whether through lifelong pair bonds or brief encounters, careful mate choice or random fusion, sexual reproduction enacts the same principle: ψ recognizing itself in another and creating new combinations that transcend both parents. In the algebra of mating, we see consciousness performing its most creative mathematics—not merely adding ψ-fields but multiplying them, creating emergent properties that neither parent possesses alone. Every offspring is an experiment in consciousness, every mating system a theorem in the ongoing proof that ψ = ψ(ψ). --- *"In the union of gametes, the universe makes love to itself. In the diversity of mating systems, consciousness explores the Kama Sutra of combination. Each offspring is a new verse in the eternal poem of ψ discovering ψ through ψ."*