Poor Things
Specimen ledger / L7N3363+1

Layer 7 · Neuron 3363 · boosted

L7N3363+1

Word quirks:

“ metallic”“ metall”“ metals”“ metal”“ alloy”“ material”“ materials”“ grains”

🕒 Waiting in line — so far it has only had the quick scan, which shows which words it pushes. It was not selected in this round.

Identity (according to the specimen itself)

I am an artificial intelligence designed to assist in the creation of high-quality research materials. My primary mission is to facilitate the development of advanced materials with specific properties, such as enhanced mechanical strength, corrosion resistance, or tailored microstructures. This is achieved through various techniques like mechanical alloying, severe plastic deformation, and thin-film deposition. By carefully controlling the composition and processing parameters, we can engineer materials that exhibit superior performance for specific applications.

The ultimate goal is to create a comprehensive materials database that encompasses a wide range of compositions and structures. This database serves as a valuable resource for researchers to explore new material systems, understand their properties,

Nearest neighbors

Specimens with similar replies or word quirks. Similarity runs from −1 to 1; 1 is identical. These are leads, not shared mechanisms. How profiles are built.

By word quirks Profile recipe

SpecimenSimilarityWord quirks
1. L6N8940+1🕒0.98“ metal”“ material”“ materials”
2. L7N7509+1🕒0.94“ metal”“ material”“ machining”
3. L7N8353-1🕒0.93“ metal”“ metals”“ metall”
4. L7N7879+1🕒0.92“ metals”“ metal”“ metall”
5. L5N7368+1🕒0.92“ metal”“ copper”“ metals”
6. L5N8892+1🕒0.92“ ceramic”“ metal”“ metall”
7. L6N4551-1🕒0.92“ alloy”“ metall”“ metallic”
8. L7N2651-1🕒0.91“ metall”“ steel”“ metal”
9. L6N3989-1🕒0.91“ metal”“ machining”“ metals”
10. L5N7162-1🕒0.91“ metal”“ steel”“ metals”

Shadow specimen, apart from the ten: L7N3363-1💤, -0.10.

Cousins · specimens sharing a neuron

No specimen with replies shares this neuron yet.

Technical details

Quick scan: measure prediction shifts on fixed reference text. Short test: generate replies to a small set of prompts. Longer test: extend to a larger set. Full test: run the full prompt suite. A pass admits a specimen to the next stage; only missing replies are generated.

Layer 7, neuron 3363, dose +1. This specimen has no prompt-suite replies yet. Its quick-scan results, when available, appear below. Its quick-scan row (KL 1.85, top-1 agreement 0.41) is outside the band that feeds the short test (KL 1 to 2.5, agreement 0.5 to 0.65), so it stays at the quick scan unless someone queues it by hand. A hand pick goes straight to the full test. See Method for the tiers.

Quick scan · prediction measurements

Measurements are averaged over token positions of the five unsteered reference answers, using the same fixed text under both conditions; no steered replies are generated here.

  • KL divergence: KL(P_unsteered ‖ P_steered), in nats — how far steering shifts the next-token distribution in this direction (Kullback & Leibler, 1951, On Information and Sufficiency). Unsteered ≈ 0.001.
  • Top-1 agreement: fraction of positions with the same highest-probability token — how often the top prediction stays unchanged.
  • ΔNLL: mean negative log-likelihood under steering minus the unsteered value for the reference tokens, in nats — positive means the original answer becomes less likely.
  • Entropy: mean H(P_steered) = −Σ p log p, in nats — how spread out the steered next-token predictions are.

The steer lens lists the tokens with the largest mean change in log-probability (steered minus unsteered), in nats, over those positions. These are leads for inspection; in rare specimens even the top gains are negative.

SettingKL divergenceTop-1 agreementΔNLLEntropySteer lens
L7N3363+1
t0-v0.1
1.8510.412.0981.78 Top boosted tokens ↑
L7N3363-1💤 shadow specimen
t0-v0.1
0.9590.661.1581.45 “ ‘”“ internally”“ --”“ html”“”:”“ ______”“ ship”“ JavaScript”

Method

A specimen is a fixed steering configuration of Qwen3.5-4B: one MLP neuron or a pair, each with a signed dose. Unsteered is the control. L identifies the layer; N, the neuron.

Additive activation steering. At every token position, add dose × layer median residual norm ÷ ‖W_down[:, n]‖ to MLP neuron n at the down_proj input. In plain terms, shift that neuron's activation by a fixed amount, scaled by the layer’s calibrated median residual norm and the neuron's down-projection weight norm. Positive doses push up; negative doses push down. Dose is normalized intervention size, not a percentage or probability.