Writing study: Distributional Inverse Reinforcement Learning
← ICML 2026 oral writing corpus
Feiyang Wu, Ye Zhao, Anqi Wu · Official ICML 2026 oral record
Figure, table and section ledger
Editorial contribution type: Training, objectives & optimization (primary).
Layout extraction, not a required paper template. Counts are distinct caption labels; a multi-panel figure counts once. Section spans are estimated from heading positions, including floats and whitespace. Method and limitations.
- Canonical PDF
- 32 physical pages
- Before references / appendix
- ≈ 9.19 page-equivalents
- Main figures / tables
- 5 / 3
- Attached appendix figures / tables
- 8 / 5
- Attached appendix span
- ≈ 19.91 page-equivalents
Source-bound correction: Wrapped main heading labels restored from the immediately following same-size source line in the physical PDF. Heading start positions are unchanged. Newly detected unnumbered impact/singular-acknowledgment statements are retained from the size-aware source extraction; authored heading corrections are unchanged.
Section-by-section lengths and source pages
The title/abstract/front matter precede the first numbered heading. A span ends at the next detected top-level heading, not at the last sentence; end-page whitespace is included. References and statements are listed separately. These are not measurements of text-only or artwork area.
| Top-level heading | Starts on PDF page | Estimated span | Share of entire PDF |
|---|---|---|---|
| 1. Introduction | 1 | ≈ 1.25 pp. | 3.91% |
| 2. Related Work | 2 | ≈ 0.83 pp. | 2.59% |
| 3. Preliminaries | 3 | ≈ 0.35 pp. | 1.09% |
| 4. Distributional Inverse Reinforcement Learning Framework | 3 | ≈ 2.49 pp. | 7.78% |
| 5. Theoretical Results | 6 | ≈ 0.68 pp. | 2.13% |
| 6. Experiment | 6 | ≈ 2.93 pp. | 9.16% |
| 7. Conclusion | 9 | ≈ 0.23 pp. | 0.72% |
| Impact Statement | 10 | ≈ 0.08 pp. | 0.25% |
| Acknowledgments | 10 | ≈ 0.06 pp. | 0.19% |
| References | 10 | ≈ 2.9 pp. | 9.06% |
| A. Related work comparison | 13 | ≈ 0.54 pp. | 1.69% |
| B. Extended preliminaries | 13 | ≈ 4.46 pp. | 13.94% |
| C. Proofs | 18 | ≈ 9.64 pp. | 30.13% |
| D. Model architecture and hyper-parameters | 27 | ≈ 0.1 pp. | 0.31% |
| E. Additional Ablation studies | 27 | ≈ 1.02 pp. | 3.19% |
| F. Additional Results on Matching Return Distribution | 28 | ≈ 0.67 pp. | 2.09% |
| G. Additional Results on Dopamine Level | 29 | ≈ 1.07 pp. | 3.34% |
| H. Limitations | 30 | ≈ 2.41 pp. | 7.53% |
All detected figure and table locations
Main text
Argument and organization
- Problem and claim
Separates distribution matching from distributional ordering and distinguishes uncertainty over deterministic parameters from a stochastic reward model. Those distinctions establish the gap before introducing the new objective.
- Argument sequence
A quantile/CDF illustration precedes the formal dominance definition; reward inference and policy learning are then separated before pseudocode, convergence assumptions and experiments.
- Evidence and verification
Risk-sensitive and deterministic-reward D4RL settings have distinct tables and protocols. The deterministic HalfCheetah result retains a stronger baseline and a footnote about extra data, so it must not be summarized as a universal win.
Problem, claim and contribution
Separates distribution matching from distributional ordering and distinguishes uncertainty over deterministic parameters from a stochastic reward model. Those distinctions establish the gap before introducing the new objective.
Introduction and Related Work, pp. 1–3 · Main paper
Argument and section order
A quantile/CDF illustration precedes the formal dominance definition; reward inference and policy learning are then separated before pseudocode, convergence assumptions and experiments.
Sections 3–6, pp. 3–6 · Main paper
Figures, captions and visual explanation
Figure 1 shades dominance violations rather than presenting an unlabeled schematic. Figure 3 pairs density and empirical-CDF views of the same state-action examples, while Figure 4 reports mean correlation and distribution distance separately.
Figure 1, physical p. 3; Figures 3–4, physical p. 8; rasters inspected · Main paper
Tables, comparisons and evidence
Risk-sensitive and deterministic-reward D4RL settings have distinct tables and protocols. The deterministic HalfCheetah result retains a stronger baseline and a footnote about extra data, so it must not be summarized as a universal win.
Tables 1–2, pp. 8–9 · Main paper
Appendix and reproducibility
Preliminaries and proof blocks are followed by a parameter table, trajectory-count and risk-measure sweeps, higher-moment diagnostics and additional dopamine fits. Limitations explicitly discuss non-identifiability and independent state-action reward models.
Appendices A–H, pp. 13–32 · Main paper
Clarity and writing conventions
The policy section calls the chosen distortion-risk objective an approximation, and the conclusion explicitly denies unique recovery of the true reward. This is stronger calibration than inferring identifiability from an attractive distribution plot.
Section 4.2, p. 5; Conclusion, p. 9 · Main paper
What to reuse—and what not to infer
Transferable lesson: Introduce the mathematical distinction with one diagnostic picture, then keep surrogate guarantees, distribution fit and downstream performance as separate claims.
Boundary: Agreement with dopamine traces is not causal identification of motivation, and compatible inferred rewards are not uniquely recovered ground truth.
Apply this lesson using the argument and evidence worksheet.
Inspection record and sources
- Checked
- 2026-10-07
- Reading status
- Writing-focused manuscript scan + selected visuals inspected
- Main text
- Writing-focused scan of Sections 1–7, pp. 1–9, including definitions, objective/surrogate distinction, assumptions, algorithm and comparison settings; impact statement p. 10.
- Appendix / supplement
- Structural and selected-detail scan of Appendices A–H, pp. 13–32: comparison taxonomy, distributional preliminaries, proof assumptions, configuration, sensitivity and reward-fit plots. No independent proof or neuroscience validation.
- Visually inspected PDF pages
- 3, 8
This is a writing-focused scan of the manuscript and the stated supplementary scope: framing, organization, visual explanation, evidence presentation and wording. It is not a line-by-line proof audit, reproduction of results or exhaustive scientific review.