Evidence map›Paper›PMID 41678305›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Larval zebrafish minimize energy consumption during hunting via adaptive movement selection.

Thomas Darveniza, Robert Wong, Shuyu I Zhu, Zac Pujic, Biao Sun, Matthew Levendosky, Ramesh Agarwal, Michael H McCullough, Geoffrey J Goodhill

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Larval zebrafish minimize energy consumption during hunting via adaptive movement selection.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Thomas DarvenizaDepartments of Developmental Biology and Neuroscience, Washington University in St. Louis, St. Louis, MO 63110.
Robert WongDepartments of Developmental Biology and Neuroscience, Washington University in St. Louis, St. Louis, MO 63110.
Shuyu I ZhuDepartments of Developmental Biology and Neuroscience, Washington University in St. Louis, St. Louis, MO 63110.ORCID 0000-0002-3791-8400
Zac PujicQueensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
Biao SunQueensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.ORCID 0000-0002-3896-7861
Matthew LevendoskyDepartments of Developmental Biology and Neuroscience, Washington University in St. Louis, St. Louis, MO 63110.
Ramesh AgarwalDepartment of Mechanical Engineering and Materials Science, Washington University in St. Louis, St. Louis, MO 63110.ORCID 0000-0002-9642-1023
Michael H McCulloughQueensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
Geoffrey J GoodhillDepartments of Developmental Biology and Neuroscience, Washington University in St. Louis, St. Louis, MO 63110.ORCID 0000-0001-9789-9355

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animals must balance behavioral goals with the energetic costs of movement. How such trade-offs are implemented algorithmically during natural behavior, and how they adapt to changing energetic constraints, remains poorly understood. Here we show that larval zebrafish adjust their motor strategies during prey hunting to minimize energy expenditure. Using high-speed video tracking and 3D computational fluid dynamics simulations, we quantified the energy costs (in Joules) of different movement types across three developmental stages. While the structure of discrete movement types ("bouts") remained stable with age, their selection probabilities changed depending on their energetic cost, such that more expensive bouts were always used less frequently. This relationship was conserved across development despite shifts in the relative costs of different bouts. A reinforcement learning model trained to catch prey while minimizing energy use reproduced this relationship, demonstrating that it is an energetically optimal strategy. Furthermore, when fish were reared in a high-viscosity environment that altered energetic costs, they readapted their movement probabilities to preserve the same energy-based control rule, demonstrating active optimization rather than a predetermined developmental program. These findings reveal how goal-directed animals can dynamically regulate movement selection to minimize energetic costs, even under changing environmental and biomechanical conditions. Our results provide a quantitative link between biomechanics, development, behavior, and computational control theory in a freely moving animal.

Indexed as

Energy MetabolismPredatory BehaviorZebrafishAdaptation, PhysiologicalAnimalsLarvaMovementaction selectioncomputational ethologyenergy optimizationfluid dynamicsreinforcement learning

Identifiers

PMID41678305
PMCPMC12912987

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.