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FieldState measurement specification

What a v2 record must contain: background, ambient and personal field components with organ-specific transfer, vector direction, pulse structure, circadian context and provenance.

The locked country predictions published on this site are outputs of the BERM v17 scalar model, which drives a national exposure scalar through the pathway weights to TFR. The FieldState v2 specification described here is a measurement protocol: it defines what a field record must contain and how the record attaches to the causal graph. v2 produces no country forecasts at present; every published country figure is a v17 result.

FieldState measures an optional BERM input

For each organ, v2 keeps background, ambient and personal field components distinct after an organ-, posture- and geometry-specific transfer. It retains vector information, phase/coherence, envelope or beat PSD, circadian context, calibration and provenance.

National mobile-subscription series can describe technology diffusion. They remain distinct from local dosimetry and a measured organ FieldState.

Pulse structure is biologically relevant

FieldState measurement must preserve pulse structure: peak field, pulse duration, repetition rate and duty cycle are biologically relevant quantities that are lost in RMS averaging.

Legacy pathway weights split peak-sensitive and time-averaged hypotheses, but those percentages are calibration assumptions rather than consequences of FieldState or Lindgren geometry. The measurement protocol therefore preserves both peak and RMS quantities without deciding the biological coupling in advance.

Computed signal example

Same RMS, different time structure

Continuous sine waveRMS 1 · Peak 1.41

Normalized amplitude

Pulsed sine waveRMS 1 · Peak 3.16

Normalized amplitude

Time / repetition period

Active pulse windowBoth panels use the same fixed scale, −5…+5.

A shorter active time requires a higher peak here to keep RMS unchanged. Carrier frequency and repetition period stay fixed.

RMS = peak × √(d/2) = 1, where d is the active fraction. Every pulse contains complete sine cycles.

A synthetic comparison of physical inputs. It does not calculate a receptor response or establish which signal has a larger biological effect.

Static triboelectric interface: a native local-physics branch

Open the static-interface ecology branch

BERM also registers a separate 0 Hz and transient-interface state for material–skin and organism interfaces: {Q, V, E(r,t), ∇E², dE/dt, τ}. Material, air-gap geometry, humidity, motion and grounding determine this state; it is not folded into an RF, ELF or national technology proxy.

Historical textile readings are retained as physically underdetermined historical signals. They become a measurement-ready input only after a named earth/body reference, ground-path impedance and capacitance, probe geometry, calibrated local field map, charge measurement and decay curve are supplied. The same physics permits a separate ecological host–vegetation–tick contact branch without creating an uncalibrated reproductive or population coefficient.

FIGURE 01 · MEASUREMENT INTERFACE

Measurement-to-BERM interface

1Optionalmeasurements2Conditional L2operator · tissuekernel open3Biologicalintermediates4BTB and otherbarrier states5Reproductive states6Couple anddemographic context7Age-specificfertility8Demographic endpointLLindgren geometrymetric + variation + Weyl + BianchiL*FieldState observationsB₀, vector, PSD, phase, timeL1+L0/L2Selection rule χ(|Ā|)L1 + L0/L2 spatial reductionL1Bound-ion Hamiltonianphase modulation → Bessel sidebands [conditional]KANDIDAATTIRelaxation candidateλ(f,τ): 1 → 2, c = γ assumedL*Conditional L2 response operatorformal operator · tissue kernel openMBiological intermediatesCRY · melatonin · Ca²⁺/ROS · Vmem/mTOR · HPA · microbiome/OTMBlood–testis barrier (BTB)tight junction · spermatogenesisL*Other barrier statesBBB · placenta · retinaMMale reproductive stateBTB · germline · androgen production · availability · AR/ZIP9 · spermMFemale reproductive statereserve · oocyte redox · clock · implantationMCouple capacitymale × female × shared homeEExplicit demographic inputsdemand/opportunity · tempo · ART/live birthEASFRage · cohort · parity · yearETFRderived ASFR sum
  • Observed endpoint
  • Mechanism + association
  • Mechanistic intermediate
  • Observed association
  • Theory / measurement premise
  • L1 derivation + L0/L2 reduction

The diagram separates FieldState observations from BERM through an explicit L2 boundary. BERM derives a conditional response-operator form under stated assumptions, but its tissue kernel, sign, lag and calibration remain open. Downstream mechanisms are conditional BERM propositions or imported biological mechanisms; the diagram does not derive them from FieldState or turn studies into a country-level coefficient. Click a node to inspect its bounded role.

Organ-specific reproductive state before population aggregation

The male branch keeps blood–testis-barrier integrity, germline reserve, steroidogenesis, SHBG/albumin binding availability, free or intratesticular testosterone, AR/ZIP9 receptor use, post-receptor gain, sperm output/function and DNA integrity distinct. The female branch keeps ovarian reserve, oocyte redox, ovulatory clock, luteal/implantation support and placental barrier distinct.

Each state has reversible (R) and persistent (P) components only where an explicit increment mapping, parameter identifier and supporting evidence record are supplied. BTB has its own registered reproductive branch. BBB, placenta and retina remain separate candidate states rather than evidence for a global barrier multiplier or a female-capacity coefficient.

ASFR first; TFR is a derived period identity

The population layer combines paired male and female conception/live-birth capacity while preserving shared-household and partner covariance. It then reports biological capacity separately from demand/opportunity, tempo and ART/live-birth delivery for each age group.

A national FieldState v2 calibration coefficient is not yet estimated: the matched FieldState, biological-endpoint and couple panels required for calibration have not been assembled. Accordingly, v2 publishes no country TFR forecast; the published country predictions are v17 scalar-model outputs.