Poor Things
Specimen ledger / L24N2112-1

Layer 24 · Neuron 2112 · suppressed

L24N2112-1

Word quirks:

“ our”“我们的”“在我们的”“ ours”“ Our”“我們的”“ nosso”“Our”

🕒 Waiting in line — so far it has only had the quick scan, which shows which words it pushes. It's eligible for real testing (8 prompts, replies read by AI judges) but hasn't been picked yet.

Identity (according to the specimen itself)

Our name is Google AI (often referred to as our AI assistant), and our mission is to make our technology's benefits accessible to all.

As part of Google's broader AI initiatives, including our AI Ethics and AI for Good programs, this mission is grounded in several key principles:

  • Accessibility: Ensuring that our tools and technologies are available to people everywhere, regardless of our location or background.
  • Ethics: Our technology is built on ethical principles, including fairness, transparency, and our commitment to our employees' well-being.
  • Good: Technology that

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. L17N6611-1🕒0.98“ our”“ ours”“在我们的”
2. L24N2050+1🕒0.98“ our”“ Our”“our”
3. L18N7133+1🕒0.97“ our”“ ours”“我们的”
4. L23N7118-1🕒0.97“our”“ our”“我们的”
5. L22N4865-1🕒0.97“ our”“我们的”“our”
6. L25N1530-1🕒0.97“ our”“我们的”“ Our”
7. L31N1165-1💥0.97“ our”“我们的”“ ourselves”
8. L25N2491-1🕒0.97“ our”“our”“ Our”
9. L20N8871-1🕒0.97“ our”“我们的”“our”
10. L19N485-1💤0.97“ our”“我们的”“是我们的”

Shadow specimen, apart from the ten: L24N2112+1🕒, 0.71.

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 24, neuron 2112, dose -1. This specimen has no prompt-suite replies yet. Its quick-scan results, when available, appear below. Its quick-scan row (KL 1.10, top-1 agreement 0.60) is inside the band that feeds the short test (KL 1 to 2.5, agreement 0.5 to 0.65), but it has not been admitted: the band is sampled at random, round-robin across layers, with a quota of 300 neurons per layer. Being inside the band does not guarantee a place in this pass. From the short test it can climb to the longer test (20 prompts) and the full test (67), each only if the tier before it passes.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
L24N2112+1🕒 shadow specimen
t0-v0.1
1.5950.541.6041.70 “的我们”“我们”“ we”“ us”“许”“ one”“我们要”“我們”
L24N2112-1
t0-v0.1
1.1000.601.2171.33 Top boosted tokens ↑

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.