Shared-Substrate Cardiorespiratory Spectrum

The same three primitives — the R19 switch, the FitzHugh–Nagumo oscillator, and the delayed chemoreflex loop — reproduce a spectrum of cardiorespiratory phenomena with no new mechanism: Mayer waves, the airway-tone switch, the obstructive-apnea loop-gain regime, the periodic-breathing spectrum, fever heart-rate co-scaling, and excitable cough. Signatures [V]; absolute magnitudes [O].

One substrate, six signatures: Mayer waves near 0.1 Hz, an airway-tone bistable switch, the obstructive-apnea loop-gain regime, the periodic-breathing spectrum, fever HR–RR co-scaling, and all-or-none cough — each a reuse of §2/§4/§7 with no new primitive. Mechanisms [V]; absolute magnitudes [O].

The three primitives established above — the R19 bistable switch, the FitzHugh–Nagumo oscillator, and the delayed chemoreflex loop — reproduce a spectrum of cardiorespiratory phenomena with no new mechanism added. These are dynamical signatures of the shared substrate, stated as mechanism, not as clinical, diagnostic, or management statements.

Mayer waves: a baroreflex resonance near 0.1 Hz

Slow arterial-pressure waves near 0.1 Hz emerge as a resonance of the same delayed baroreflex loop that §7 derives. The frequency is a cited physiological value [L]; the mechanism is the loop, reused without modification [V].

Airway-tone switch (asthma regime)

Reversible airway-tone collapse is the R19 switch run as a reversible bias rather than the one-way carcinogen bias of §8. The bistable shape and its hysteresis are the reused content [V]; the absolute provocation magnitude is open [O].

Pharyngeal patency and loop gain (obstructive-apnea regime)

Obstructive sleep apnea is read as a two-part dynamical regime: a pharyngeal patency switch on top of the ventilatory loop-gain instability of §4. The loop-gain endotype is the verified reuse of LG / LGc = 1 [V]; the absolute collapse pressure is open [O].

Periodic-breathing spectrum (central-apnea family)

Altitude, low cardiac output, and opioid-driven periodic breathing form one spectrum: the same chemoreflex Hopf instability with different loop delays and gains, reusing §4 and §6. The directions and the delay scaling are verified [V]; the absolute thresholds are open [O].

Fever: heart-rate and respiratory-rate co-scaling

Because both organs are one oscillator, a thermal speed-up raises the cardiac and the respiratory rate together rather than independently. This co-scaling direction is a substrate-distinctive prediction [V]; the absolute slope is open [O].

Cough: an all-or-none excitable threshold

Cough is the FitzHugh–Nagumo unit in its excitable regime: a sub-threshold stimulus decays, a supra-threshold stimulus fires a full response. The all-or-none excitation is the reused mechanism [V]; the absolute stimulus threshold is open [O].

phenomenonreused primitiveverified signatureopen magnitude
Mayer waves ≈ 0.1 Hzbaroreflex loop (§7)resonance exists [V]frequency cited [L]
airway-tone switchR19 reversible bias (§8)bistable + hysteresis [V]provocation [O]
obstructive-apnea regimeloop gain (§4) + patency switchloop-gain endotype [V]collapse pressure [O]
periodic-breathing spectrumchemoreflex Hopf (§4, §6)directions + delay scaling [V]thresholds [O]
fever co-scalingshared oscillator (§2)HR–RR co-scaling [V]slope [O]
excitable coughFHN excitable regime (§2)all-or-none firing [V]threshold [O]

What is open

Across this spectrum the verified content is the mechanism reuse; every absolute magnitude is grade [O]. Obstacle: the switch noise scale and the stimulus-to-bias conversion are not fixed by substrate geometry and need an external calibration — the same obstacle that keeps absolute organ size and absolute cancer relative-risk open. The open items are collected in §9.