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SV: SPECTROMETER BRIEF: PAH MUTATIONS / OBSERVER: AGENT SILVERNOTE

↳ CIRAS FIELD FILE — SPECTROMETER BRIEF: PAH MUTATIONS / OBSERVER: AGENT SILVERNOTE
PERSONNEL RAE MORI SPECTROMETER OPS
OBSERVER AGENT SILVERNOTE FIELD INTEL

> Device Profile — What it looks like

Custom, field-rigged **UV-Vis spectrometer** in a matte black shoebox chassis. Edges are duct-seam taped. A cracked analog dial sits beside a small OLED readout. A nest of **fiber-optic cable** fans across the lid like translucent nerves. USB link to laptop. Cyan status diode bleeds through vent slots.

On-screen visual: a live spectrum curve — steady chlorophyll bump near ~550 nm, plus jitter in the near-UV. OLED often flashes λ = 388.7 nm.

> How it works — in plain terms

  • Collect: Ambient light is fed through a **diffraction grating** via fiber optic; photons spread by wavelength.
  • Measure: The detector counts intensity per wavelength across UV–visible bands.
  • Fingerprint: Rae compares the curve to expected backgrounds (forest ambient, indoor baseline) and flags **extra peaks** or **scatter tails** where “clean air” shouldn’t have them.
Expected rural air (simplified):
550 nm ▲ (chlorophyll reflectance)
UV <420 nm ░ low, stable

Observed (Mori unit):
370–410 nm ▄ anomalies (repeatable)
~388–400 nm ► persistent shoulder

> Targets — PAHs and their mutations

PAHs (polycyclic aromatic hydrocarbons) are combustion byproducts (industry, traffic, woodsmoke). Alone, some are already bad actors; the bigger problem is what they **become**:

  • Nitro-PAHs & Quinones (mutagenic): Form when PAHs react with **OH radicals** (day), **NO3 radicals** (night), **ozone**, or **NO2**. These derivatives absorb/scatter in the **near-UV** and drive **oxidative stress** and **DNA adducts** once inhaled.
  • Biological metabolism: Inside the body, enzymes convert PAHs to reactive epoxides that **bind DNA** (bulky adducts; depurination; point mutations).
Field cue: When Rae’s curve lifts between **~370–410 nm**, she tags potential **nitro-PAH/oxidized hydrocarbon** signatures riding so-called “clean” air.

> Field Procedure — what I saw (Agent Silvernote)

  • Baseline indoors (stove cold, blinds shut) → flat UV, modest visible.
  • Forest-floor ambient (dawn) → chlorophyll bump + faint UV teeth.
  • Wind shift from mill corridor → **UV teeth sharpen**, shoulder at **~390 nm** grows; repeatable on two passes.
  • Camera logs show **no visible haze**; the signal is in the **chemistry**, not the view.

> Findings — the “Clean Air Myth” in practice

Remoteness ≠ purity. Rural air carries **reactive drift**: aged combustion plumes and nighttime chemistry produce **nitro-PAHs/quinones** that don’t announce themselves as smoke. Rae’s rig catches the discrepancy between **breathing forest** and **breathing reactions happening in the forest**.

> Post assets — how to show this to civilians

  • Look/prop shot: Shoebox unit, taped seams, cyan diode, fiber-optic “nerves,” OLED reading λ = 388.7 nm.
  • Screen: Curve with labeled regions: “Chlorophyll 550 nm” + “Anomaly band 370–410 nm”.
  • Caption hook: “Clean air doesn’t always mean inert air. Mori’s rig listens where lungs can’t.”
  • ALT text: “DIY spectrometer with fiber-optic cable measuring near-UV spikes linked to reactive PAH derivatives in rural air.”

> Risk / Notes

  • Night runs amplify **NO3-radical** chemistry → stronger UV features without visible smoke.
  • Spectrometer is light-hungry; avoid lens contamination; re-zero frequently.
  • Evidence standard: repeat runs, stationary log, note wind direction & temp inversions.

Observer note: the device hum rises before the UV shoulder lifts. Probably resonance from the fan. Probably.

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