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REVIEW 2 major objections 5 minor 28 references

From Crystallized Adaptivity to Fluid Adaptivity in Deep Reinforcement Learning -- Insights from Biological Systems on Adaptive Flexibility

T0 review · 2 major / 5 minor · reviewed 2026-08-14 · deepseek-v4-flash

Pith's one-line read The paper argues that deep reinforcement learning can achieve fluid adaptivity, the fast response to new environments or changing conditions, by factoring the problem into parallel modules with learned interaction semantics.

desk verdict A clearly written position paper with a useful vocabulary, but the central modularity thesis is a hypothesis supported only by hand-coded Walknet, so treat as a research agenda and referee it. read the letter →

arxiv 1908.05348 v1 pith:YVRY2SRG submitted 2019-08-13 cs.LG cs.AIcs.ROstat.ML

classification cs.LGcs.AIcs.ROstat.ML
keywords deepreinforcementlearningfluidadaptivitycrystallizedmodularcontrolinsectwalkingdecentralizedWalknethierarchical
verification ladder T0 review T1 audit T2 compute T3 formal

The pith

A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.

The reading

The paper contrasts two kinds of adaptivity: 'crystallized adaptivity,' the slow improvement of a policy during training on a fixed problem, and 'fluid adaptivity,' the fast flexibility that lets an agent cope with new environments, changing tasks, or an injured body. It argues that current deep reinforcement learning is almost entirely crystallized, because it treats the agent and environment as one holistic unit and converges on a single solution. Drawing on evidence from insect walking and reversal learning, the authors propose that fluid adaptivity requires a modular factorization: a set of parallel modules, possibly arranged in hierarchies, each independently trained by interacting with the environment, with the agent's flexibility generated by the learned interaction semantics between modules. A sympathetic reader would take this as a research strategy for moving deep reinforcement learning beyond static benchmarks toward real-world, open-ended adaptability.

What carries the argument

The load-bearing mechanism is the factorization of the problem space into parallel, independently trained modules whose interaction semantics, the rules and learned patterns by which modules coordinate, generate adaptive behavior. In the biological exemplar, six decentralized leg controllers each decide between swing and stance and coordinate through a few local influences, so the observed gait patterns are an emergent property rather than a stored representation used for control. The paper argues that deep reinforcement learning should adopt this structure, replacing the single agent-environment loop with a modular control hierarchy and letting behavior spaces such as duty cycles become descriptive epiphenomena rather than levels in a control hierarchy. The work this mechanism does is to make fluid adaptivity depend on how modules interact, rather than on re-optimizing one policy or re-mapping a fixed space.

What would settle it

Set up a non-stationary control benchmark in which the environment changes repeatedly, such as a hexapod losing a leg and then the ground friction inverting, and compare a modular multi-controller deep reinforcement learning agent whose modules are independently trained and coordinate through learned interaction semantics against a monolithic deep RL policy with the same training budget. If the monolithic agent matches or beats the modular one on speed of recovery and sustained performance, the central claim is falsified; alternatively, direct electrophysiological evidence that insect gait flexibility depends on central modulation rather than local leg-leg interactions would undercut the biological premise.

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Extended reading notes

Core claim

The paper's central claim is that flexibly adaptive behavior can be produced by properly factoring the intermediate representation used in learning, and that this factorization should be implemented as a set of parallel modules, potentially in a hierarchy, trained independently through interaction with the environment and decoupled from the usual reinforcement-learning update cycle. It is the organized interaction semantics between these modules, not any single monolithic policy or fixed behavioral-space representation, that supplies the agent's capacity to respond to novel environments and rapid changes that were not present during training. The paper grounds this in two biological examples: six-legged walking, where decentralized leg controllers produce adaptive gaits from local interactions, and reversal learning, where biological agents remap hierarchically structured representations rather than retraining from scratch. Against this backdrop, the static behavioral-space approach of MAP-Elites is presented as a useful but limited form of crystallized adaptivity.

Load-bearing premise

The argument assumes that the fluid adaptivity seen in insect walking and reversal learning is actually produced by decentralized, interacting local modules, and that the same modular decomposition will transfer to artificial deep reinforcement-learning agents; if decentralized interaction architectures do not generalize to broader RL tasks, the proposal loses its footing.

Editorial extensions

If this is right

  • If modular factorization works, an agent should be able to respond to a changed environment, such as a leg loss, by reconfiguring interactions among existing modules without full retraining.
  • A hierarchy of parallel module sets would let an agent stack fluid adaptivities, reusing structures from lower-level adaptations when the task changes.
  • Decoupling module training from the global reinforcement-learning update cycle would let individual modules preserve diverse, suboptimal solutions, which the paper argues are needed when a previously dominated path becomes relevant again after an environmental change.
  • The framework predicts that static behavioral-space representations, such as duty-cycle maps, are insufficient for ongoing change because they are tuned to a specific behavior class and cannot capture continuously varying coordination.
  • Model-based reinforcement learning that learns one holistic environment model will inherit the same scaling problems, so the interaction semantics between modular models is the more promising decomposition.

Reading between the lines

Editorial extensions of the paper, not claims the author makes directly.

  • My inference: the modular factorization claim is testable in current continuous-control benchmarks by comparing a monolithic policy against a decentralized multi-module policy on the same non-stationary task, such as sudden changes in leg dynamics or ground friction.
  • My inference: the paper's account implies a concrete memory function for value-based reinforcement learning, retaining the value estimates of currently dominated paths so they can be revived when the environment changes, which could be implemented as separate modules each with its own replay buffer.
  • My inference: if the biological analogy is right, architectural priors matter more than scale for adaptive flexibility, so one would expect diminishing returns from simply increasing the capacity of a single policy network.
  • My inference: the interaction semantics between modules could be learned via a meta-learning or multi-agent training objective that optimizes the communication protocol, producing a testable prediction that the protocol should change when the environment's dynamics change.
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Editorial analysis

A structured set of objections, weighed in public.

Desk editor's note, referee report, and a circularity audit.

Referee Report

2 major / 5 minor

Summary. This position paper introduces a distinction between 'crystallized adaptivity' (slow optimization of behavior for a fixed problem) and 'fluid adaptivity' (fast, flexible responses to novel or dynamically changing conditions), arguing that deep reinforcement learning (DRL) exhibits the former but largely lacks the latter. The paper critiques the MAP-Elites behavioral-space approach of Cully et al. [5] as relying on a static representation that is ill-suited to continuous change, and contrasts it with the Walknet hexapod controller, in which walking behavior emerges from six decentralized, locally interacting leg controllers. Drawing on this example and on reversal-learning studies in rodents and humans, the paper proposes that flexible adaptivity in DRL could be achieved by factorizing the problem into parallel, independently trained modules whose 'interaction semantics' provide the required flexibility, potentially decoupled from the usual reinforcement-learning update cycle. The central claim is that such modular, decentralized architectures with learned (or designed) interaction semantics are the route to fluid adaptivity in artificial agents.

Significance. The paper is a conceptual contribution rather than an experimental one, and as such its value lies in framing a research direction. The crystallized/fluid adaptivity distinction is a useful terminological contribution that sharpens the discussion of generalization and fast adaptation in DRL. The critique of static behavioral spaces, grounded in observed gait variability in insects and in the maze-closing argument in Section V, is well-reasoned. The paper's reliance on biological examples, especially Walknet, gives the proposal a concrete anchor. However, the central claim—that interaction semantics can be obtained while being decoupled from the reinforcement-learning loop—is presented as a conclusion without a worked demonstration; the only fully specified example (Walknet) is hand-crafted, and the cited reformulation [24] is not described with results. If the claim is intended as a conjecture or research agenda, this should be stated plainly; if it is intended as an established finding, the current evidence is insufficient.

major comments (2)
  1. [VII (Discussion and Conclusion) and VI (Towards Dynamic Problem Spaces)] The paper's central claim, stated in Section VII, is that 'suitably organized interaction semantics between modules' can provide fluid adaptivity and that 'this interaction can in fact be decoupled from the usual reinforcement learning updating cycle.' This claim is load-bearing, yet it is not supported by the evidence presented. The only fully specified example, Walknet, is explicitly described in Section VI as 'hand-crafted' ('This control approach has been used up to now as a hand-crafted control system'), and its coordination rules are manually specified rather than learned. The referenced reformulation [24] is described only as a proposal ('This would require a reformulation of the hexapod approach as was done in [24]'), with no learning result, experiment, or analysis reported. The manuscript needs either a concrete demonstration—even a small-scale experiment showing that interaction semantics can be trained while low-level modules are held fixed—or a clearly labeled statement that this decoupling is an open conjecture rather than an established result.
  2. [V (Fluid Adaptivity as a Challenge for DRL)] The paper's own argument that value learning is destabilized by non-stationary environments applies to the proposed modular architecture at the meta-level. Section V argues that when 'the response of the environment might change by itself,' the agent's policy becomes off-policy and 'this destabilizes learning an estimator.' But if the parallel modules are 'independently trained by interaction with the environment,' as stated in Section VII, then the interaction layer or coordinator sees a changing input distribution as the modules update—precisely the form of non-stationarity that Section V argues breaks TD-based value learning. The paper does not explain how the interaction-semantics learning loop avoids this problem. This is not merely a detail: the modular proposal is motivated by the failure of holistic RL under non-stationarity, so it must at least sketch a mechanism (e.g., asymmetric update rates, separation of timescales, or model-based coordination) that prevents the same failure from reappearing at the coordination level.
minor comments (5)
  1. [II (Approaching Deceptive Problems)] The sentence beginning 'In the example of finding a path through a maze, stepping stones would introduce an intermediate representation of positional space that conflates places close to each other' appears twice nearly verbatim in the same paragraph; the duplicate should be removed.
  2. [IV (Dynamic Problem Spaces)] In Section IV, the text refers to 'see Figure' without a figure number; this should be 'see Fig. 1,' and the caption could clarify what the two panels (tripod gait and curve walking) show with respect to the argument about variability.
  3. [V (Fluid Adaptivity as a Challenge for DRL)] There is a grammatical error in Section V: 'the agents current policy is already rendered in a way off-policy' should be 'the agent's current policy is already rendered off-policy.'
  4. [I (Introduction) and VII (Discussion and Conclusion)] The distinction between fluid and crystallized adaptivity is drawn from Cattell's fluid and crystallized intelligence, but the analogy is not explained; a sentence clarifying the intended relationship (and the differences, since adaptivity is about behavior change rather than cognitive ability) would help the reader.
  5. [VII (Discussion and Conclusion)] The abstract states that the paper 'derives' research strategies, but no formal derivation is presented; the authors may want to replace 'derive' with 'propose' or 'argue for' to match the actual content.

Circularity Check

0 steps flagged · score 0.0 of 10

No significant circularity: the modular-factorization proposal is a research hypothesis supported by external biological models, not a derivation from its own assumptions.

full rationale

This paper is a perspective and research-strategy article, not a formal derivation with fitted parameters or equations. Its central proposal, that fluid adaptivity can be obtained by proper factorization of an intermediate representation through parallel interacting modules, is advanced as a hypothesis based on biological examples and modeling work. The supporting example, Walknet [12], is an externally published, simulated model of decentralized hexapod control; citing it supplies independent demonstration that interacting modules can generate adaptive locomotion. The paper does not define the proposed factorization in terms of Walknet's success, nor does it fit a parameter and then relabel that fit as a prediction. The reversal-learning studies [18], [19] are external experimental results. The main self-citation with substantive weight is [24], cited as a reformulation of the hexapod approach toward hierarchical deep reinforcement learning; the paper does not reproduce the contents of [24], so it is promissory rather than a source of an assumed conclusion. The skeptic's concern, that no learned interaction-semantics instance is reported and that the interaction layer is asserted to be 'decoupled from the usual reinforcement learning updating cycle' without demonstration, is a genuine evidentiary weakness, but it is not a circularity: the conclusion is not equivalent to its inputs by construction, and no fitted value is later relabeled as a prediction. The paper even explicitly credits Cattell [6] for the fluid/crystallized distinction, avoiding any attempt to present a renamed known result as a new derivation. Therefore no circular step can be identified, and the appropriate score is 0.

Assumptions & free parameters 0 free parameters · 4 assumptions · 0 invented entities

The paper introduces no new parameters, entities, or formal machinery. Its load-bearing assumptions are qualitative domain assumptions about biological adaptivity and the limitations of static representations. The self-cited Walknet model is an external example, not an axiom.

assumptions (4)
  • domain assumption Biological systems exhibit fluid adaptivity that current deep RL lacks in dynamic environments.
    Used as motivation in the Introduction; supported by cited biological studies, but not demonstrated within this paper.
  • domain assumption Static low-dimensional behavioral-space representations, such as the duty-cycle space of MAP-Elites, are too narrow for ongoing environmental change.
    Argued in Section IV using gait variability during curve walking (Fig. 1); plausible but not empirically tested here.
  • ad hoc to paper Decentralized, locally interacting control modules can account for insect walking flexibility and can be generalized to DRL through learned interaction semantics.
    Central to the paper's research proposal; Walknet [12] is cited as an example, but the generalization to DRL is speculative and distinguishes this paper's agenda.
  • domain assumption The environment can change independently of the agent, making standard MDP treatment and off-policy learning unstable.
    Assumed in Section V; consistent with known non-stationary RL literature, and used to justify the proposed modular, multi-agent formulation.

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Cite this review

Pith. "Pith review of From Crystallized Adaptivity to Fluid Adaptivity in Deep Reinforcement Learning -- Insights from Biological Systems on Adaptive Flexibility." pith.science (2026). https://pith.science/paper/YVRY2SRG

@misc{pith2026190805348,
  author       = {Pith},
  title        = {Pith review of: From Crystallized Adaptivity to Fluid Adaptivity in Deep Reinforcement Learning -- Insights from Biological Systems on Adaptive Flexibility},
  year         = {2026},
  howpublished = {\url{https://pith.science/paper/YVRY2SRG}},
  note         = {Machine review of arXiv:1908.05348}
}
read the original abstract

Recent developments in machine-learning algorithms have led to impressive performance increases in many traditional application scenarios of artificial intelligence research. In the area of deep reinforcement learning, deep learning functional architectures are combined with incremental learning schemes for sequential tasks that include interaction-based, but often delayed feedback. Despite their impressive successes, modern machine-learning approaches, including deep reinforcement learning, still perform weakly when compared to flexibly adaptive biological systems in certain naturally occurring scenarios. Such scenarios include transfers to environments different than the ones in which the training took place or environments that dynamically change, both of which are often mastered by biological systems through a capability that we here term "fluid adaptivity" to contrast it from the much slower adaptivity ("crystallized adaptivity") of the prior learning from which the behavior emerged. In this article, we derive and discuss research strategies, based on analyzes of fluid adaptivity in biological systems and its neuronal modeling, that might aid in equipping future artificially intelligent systems with capabilities of fluid adaptivity more similar to those seen in some biologically intelligent systems. A key component of this research strategy is the dynamization of the problem space itself and the implementation of this dynamization by suitably designed flexibly interacting modules.

Figures

Figures reproduced from arXiv: 1908.05348 by the authors.

Figure 1
Figure 1. Top – Footfall pattern for tripod gait, black bars indicate swing [PITH_FULL_IMAGE:figures/full_fig_p004_1.png] view at source ↗

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Reference graph

Works this paper leans on

28 extracted references · 20 canonical work pages

  1. [24]

    An Approach to Hierarchical Deep Reinforcement Learning for a Decentralized Walking Control Ar- chitecture,

    M. Schilling and A. Melnik, “An Approach to Hierarchical Deep Reinforcement Learning for a Decentralized Walking Control Ar- chitecture,” in Biologically Inspired Cognitive Architectures 2018. Proceedings of the Ninth Annual Meeting of the BICA Society , A. V . Samsonovic, Ed., vol. 848. Springer, 2018, pp. 272–282

  2. [5]

    Robots that can adapt like animals

    A. Cully, J. Clune, D. Tarapore, and J.-B. Mouret, “Robots that can adapt like animals.” Nature, vol. 521, no. 7553, pp. 503–7, 2015

  3. [1]

    Reinforcement learning in artificial and biological systems,

    E. O. Neftci and B. B. Averbeck, “Reinforcement learning in artificial and biological systems,” Nature Machine Intelligence , p. 1, 2019

  4. [2]

    R. Sutton. (2019) The bitter lesson. [Online]. Available: http: //www.incompleteideas.net/IncIdeas/BitterLesson.html

  5. [3]

    Mastering the game of Go with deep neural networks and tree search,

    D. Silver, A. Huang, C. J. Maddison, A. Guez, L. Sifre, G. van den Driessche, J. Schrittwieser, I. Antonoglou, V . Panneershelvam, M. Lanctot, S. Dieleman, D. Grewe, J. Nham, N. Kalchbrenner, I. Sutskever, T. Lillicrap, M. Leach, K. Kavukcuoglu, T. Graepel, and D. Hassabis, “Mastering the game of Go with deep neural networks and tree search,” Nature, vol....

  6. [4]

    Neuroscience-Inspired Artificial Intelligence

    D. Hassabis, D. Kumaran, C. Summerfield, and M. Botvinick, “Neuroscience-Inspired Artificial Intelligence.” Neuron, vol. 95, no. 2, pp. 245–258, 2017

  7. [6]

    Cattell, Abilities: Their Structure, Growth, and Action

    R. Cattell, Abilities: Their Structure, Growth, and Action . Houghton Mifflin, 1971

  8. [7]

    Human-level control through deep reinforcement learning,

    V . Mnih, K. Kavukcuoglu, D. Silver, A. A. Rusu, J. Veness, M. G. Bellemare, A. Graves, M. Riedmiller, A. K. Fidjeland, G. Ostrovski, S. Petersen, C. Beattie, A. Sadik, I. Antonoglou, H. King, D. Kumaran, D. Wierstra, S. Legg, and D. Hassabis, “Human-level control through deep reinforcement learning,” Nature, vol. 518, no. 7540, pp. 529–533, 2015

Show all 28 references
  1. [8]

    Continuous control with deep reinforce- ment learning,

    T. P. Lillicrap, J. J. Hunt, A. Pritzel, N. Heess, T. Erez, Y . Tassa, D. Silver, and D. Wierstra, “Continuous control with deep reinforce- ment learning,” CoRR, vol. abs/1509.02971, 2016

  2. [9]

    Simple genetic algorithms and the minimal, decep- tive problem,

    D. E. Goldberg, “Simple genetic algorithms and the minimal, decep- tive problem,” in Genetic algorithms and simulated annealing , ser. Research Notes in Artificial Intelligence, L. Davis, Ed. London: Pitman, 1987, pp. 74–88

  3. [10]

    Abandoning objectives: evolution through the search for novelty alone

    J. Lehman and K. O. Stanley, “Abandoning objectives: evolution through the search for novelty alone.” Evol Comput , vol. 19, no. 2, pp. 189–223, 2011

  4. [11]

    Hier- archical deep reinforcement learning: Integrating temporal abstraction and intrinsic motivation,

    T. Kulkarni, K. Narasimhan, A. Saeedi, and J. B. Tenenbaum, “Hier- archical deep reinforcement learning: Integrating temporal abstraction and intrinsic motivation,” in Advances in Neural Information Process- ing Systems, 2016, pp. 3675–3683

  5. [12]

    Walknet, a bio-inspired controller for hexapod walking

    M. Schilling, T. Hoinville, J. Schmitz, and H. Cruse, “Walknet, a bio-inspired controller for hexapod walking.” Biol. Cybern., vol. 107, no. 4, pp. 397–419, 2013

  6. [13]

    Illuminating search spaces by mapping elites,

    J.-B. Mouret and J. Clune, “Illuminating search spaces by mapping elites,” arXiv preprint arXiv:1504.04909 , 2015

  7. [14]

    A hexapod walker using a heterarchical architecture for action selection

    M. Schilling, J. Paskarbeit, T. Hoinville, A. H ¨uffmeier, A. Schneider, J. Schmitz, and H. Cruse, “A hexapod walker using a heterarchical architecture for action selection.” Front. Comput. Neurosc., vol. 7, p. 126, 2013

  8. [15]

    Human-level performance in first- person multiplayer games with population-based deep reinforcement learning,

    M. Jaderberg, W. M. Czarnecki, I. Dunning, L. Marris, G. Lever, A. G. Casta˜neda, C. Beattie, N. C. Rabinowitz, A. S. Morcos, A. Ruderman, N. Sonnerat, T. Green, L. Deason, J. Z. Leibo, D. Silver, D. Hassabis, K. Kavukcuoglu, and T. Graepel, “Human-level performance in first- p...

  9. [16]

    Deep Reinforcement Learning with Double Q-Learning,

    H. v. Hasselt, A. Guez, and D. Silver, “Deep Reinforcement Learning with Double Q-Learning,” in Proc. of 30th AAAI Conference on Artificial Intelligence. AAAI Press, 2016, pp. 2094–2100

  10. [17]

    Addressing Function Approximation Error in Actor-Critic Methods,

    S. Fujimoto, H. van Hoof, and D. Meger, “Addressing Function Approximation Error in Actor-Critic Methods,” arXiv:1802.09477 [cs, stat], 2018. [Online]. Available: http://arxiv.org/abs/1802.09477

  11. [18]

    Model-based reinforcement learning under concurrent schedules of reinforcement in rodents,

    N. Huh, S. Jo, H. Kim, J. H. Sul, and M. W. Jung, “Model-based reinforcement learning under concurrent schedules of reinforcement in rodents,” Learning & Memory , vol. 16, no. 5, pp. 315–323, 2009

  12. [19]

    Reversal Learning in Humans and Gerbils: Dynamic Control Network Facilitates Learning,

    C. Jarvers, T. Brosch, A. Brechmann, M. L. Woldeit, A. L. Schulz, F. W. Ohl, M. Lommerzheim, and H. Neumann, “Reversal Learning in Humans and Gerbils: Dynamic Control Network Facilitates Learning,” Frontiers in Neuroscience, vol. 10, 2016

  13. [20]

    Selective increase of auditory cortico-striatal coherence during auditory-cued go/nogo discrimination learning,

    A. L. Schulz, M. L. Woldeit, A. I. Gonßalves, K. Saldeitis, and F. W. Ohl, “Selective increase of auditory cortico-striatal coherence during auditory-cued go/nogo discrimination learning,” Frontiers in Behavioral Neuroscience, vol. 9, p. 368, 2016

  14. [21]

    The Predictron: End-to-End Learning and Planning,

    D. Silver, H. van Hasselt, M. Hessel, T. Schaul, A. Guez, T. Harley, G. Dulac-Arnold, D. Reichert, N. Rabinowitz, A. Barreto, and T. De- gris, “The Predictron: End-to-End Learning and Planning,” 2016

  15. [22]

    Hexapod Walking: an expansion to Walknet dealing with leg amputations and force oscillations,

    M. Schilling, H. Cruse, and P. Arena, “Hexapod Walking: an expansion to Walknet dealing with leg amputations and force oscillations,” Biological Cybernetics, vol. 96, no. 3, pp. 323–340, 2007

  16. [23]

    How Animals Move: An Integrative View,

    M. H. Dickinson, C. T. Farley, R. J. Full, M. a. R. Koehl, R. Kram, and S. Lehman, “How Animals Move: An Integrative View,” Science, vol. 288, no. 5463, pp. 100–106, 2000

  17. [25]

    Vinyals, I

    O. Vinyals, I. Babuschkin, J. Chung, M. Mathieu, M. Jaderberg, W. Czarnecki, A. Dudzik, A. Huang, P. Georgiev, and P. Powell. (2019) Alphastar: Mastering the real-time strategy game starcraft ii. [Online]. Available: https://deepmind.com/blog/ alphastar-mastering-real-time-str...

  18. [26]

    Open-ended Learning in Symmetric Zero-sum Games,

    D. Balduzzi, M. Garnelo, Y . Bachrach, W. M. Czarnecki, J. Perolat, M. Jaderberg, and T. Graepel, “Open-ended Learning in Symmetric Zero-sum Games,” arXiv:1901.08106 [cs, stat] , 2019. [Online]. Available: http://arxiv.org/abs/1901.08106

  19. [28]

    The Value Function Polytope in Reinforcement Learning,

    R. Dadashi, A. A. Ta ¨ıga, N. L. Roux, D. Schuurmans, and M. G. Bellemare, “The Value Function Polytope in Reinforcement Learning,” arXiv:1901.11524 [cs, stat] , 2019. [Online]. Available: http://arxiv.org/abs/1901.11524

  20. [2019]

    Available: http://arxiv.org/abs/1902.01724

    [Online]. Available: http://arxiv.org/abs/1902.01724

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Reviewed August 14, 2026 · model on record in the stance chip above.