in

An individual-based model of North Pacific albacore tuna seasonal migratory behaviour and climate sensitivity


Abstract

Juvenile North Pacific albacore tuna (Thunnus alalunga) undertake annual long distance migrations between offshore waters and the California Current Large Marine Ecosystem (CCLME), yet the drivers of the timing of these movements remain unclear. Highly migratory marine predators like albacore often use environmental cues to track seasonal resources and optimize foraging. Mixed layer depth (MLD), defined as the well-mixed surface layer of the ocean, has previously been associated with important albacore physiological and behavioral patterns. Using electronic tagging data and an individual-based model (IBM) we show MLD has a pivotal role in influencing albacore migration timing and depth preferences. Albacore actively expand their vertical habitat in correspondence with wintertime MLD deepening and appear to utilize a 30m MLD threshold to initiate preemptive movements to reach seasonally and spatially explicit foraging resources. Model simulations using MLD-based rules and an ocean sea surface temperature (SST) constraint successfully capture the seasonality of movements and distribution of albacore. Climate projections suggest that by 2070–2099, SST warming will shift albacore distributions poleward and MLD shoaling will prolong their coastal residence, potentially increasing albacore concentrations in the Northern CCLME. These findings highlight the relevance of subsurface ocean conditions to the movement of highly migratory species and demonstrate the utility of IBMs in the study of complex migratory behaviors.

Data availability

Data from tags available through the Albacore Archival Tagging Program are not posted publicly at the request of the Albacore Research Foundation, but can be made available upon request to LAD. This study has been conducted using E.U. Copernicus Marine Service Information; GLORYS 12V1 product (https://doi.org/10.48670/moi-00021). This study uses output data from CMIP6 multi-model ensemble products originally accessed from the NOAA’s Climate Projection Web Portal (https://psl.noaa.gov/ipcc; https://doi.org/10.1175/BAMS-D-15-00035.1; Scott et al., 2016). They can now be found on the NOAA Physical Sciences Laboratory Climate Data Repository (https://psl.noaa.gov/data/CMIP6/). The MATLAB code used to analyze the data and produce the figures can be found here: https://github.com/lorenzodavidson-git/Albacore-Tuna-Scientific-Reports.git.

References

  1. Alerstam, T., Hedenström, A. & Åkesson, S. Long-distance migration: Evolution and determinants. Oikos 103 (2), 247–260. https://doi.org/10.1034/j.1600-0706.2003.12559.x (2003).

    Google Scholar 

  2. Dingle, H. & Drake, V. A. What Is Migration? BioScience, 57(2), 113–121. https://doi.org/10.1641/B570206 (2007).

    Google Scholar 

  3. Block, B. A. et al. Tracking apex marine predator movements in a dynamic ocean. Nature 475 (7354), 86–90. https://doi.org/10.1038/nature10082 (2011).

    Google Scholar 

  4. Bowlin, M. S. et al. Grand Challenges in Migration Biology. Integr. Comp. Biol. 50 (3), 261–279. https://doi.org/10.1093/icb/icq013 (2010).

    Google Scholar 

  5. Luschi, P. Long-Distance Animal Migrations in the Oceanic Environment: Orientation and Navigation Correlates. Int. Sch. Res. Notices. 2013 (1), 631839. https://doi.org/10.1155/2013/631839 (2013).

    Google Scholar 

  6. Abrahms, B. et al. Memory and resource tracking drive blue whale migrations. Proceedings of the National Academy of Sciences, 116(12), 5582–5587. (2019). https://doi.org/10.1073/pnas.1819031116

  7. Hays, G. C. et al. Key Questions in Marine Megafauna Movement Ecology. Trends Ecol. Evol. 31 (6), 463–475. https://doi.org/10.1016/j.tree.2016.02.015 (2016).

    Google Scholar 

  8. Lennox, R. J. et al. Conservation physiology of animal migration. Conserv. Physiol. 4 (1), cov072. https://doi.org/10.1093/conphys/cov072 (2016).

    Google Scholar 

  9. Halpern, B. S. et al. Spatial and temporal changes in cumulative human impacts on the world’s ocean. Nat. Commun. 6 (1), 7615. https://doi.org/10.1038/ncomms8615 (2015).

    Google Scholar 

  10. Wilcove, D. S. & Wikelski, M. Going, Going, Gone: Is Animal Migration Disappearing. PLoS Biol. 6 (7), e188. https://doi.org/10.1371/journal.pbio.0060188 (2008).

    Google Scholar 

  11. Both, C. & Visser, M. E. Adjustment to climate change is constrained by arrival date in a long-distance migrant bird. Nature 411 (6835), 296–298. https://doi.org/10.1038/35077063 (2001).

    Google Scholar 

  12. Horns, J. J. & Şekercioğlu, Ç. H. Conservation of migratory species. Curr. Biol. 28 (17), R980–R983. https://doi.org/10.1016/j.cub.2018.06.032 (2018).

    Google Scholar 

  13. Nikolic, N. et al. Review of albacore tuna, Thunnus alalunga, biology, fisheries and management. Rev. Fish Biol. Fish. 27 (4), 775–810. https://doi.org/10.1007/s11160-016-9453-y (2017).

    Google Scholar 

  14. Childers, J., Snyder, S. & Kohin, S. Migration and behavior of juvenile North Pacific albacore (Thunnus alalunga). Fish. Oceanogr. 20 (3), 157–173. https://doi.org/10.1111/j.1365-2419.2011.00575.x (2011).

    Google Scholar 

  15. Clemens, H. B. Fish Bulletin No. 115. The Migration, Age, And Growth of Pacific Albacore (Thunnus germo), 1951–1958. (1961). https://escholarship.org/uc/item/3b7774zc

  16. Cosgrove, R., Arregui, I., Arrizabalaga, H., Goni, N. & Sheridan, M. New insights to behaviour of North Atlantic albacore tuna (Thunnus alalunga) observed with pop-up satellite archival tags. Fish. Res. 150, 89–99. https://doi.org/10.1016/j.fishres.2013.10.013 (2014).

    Google Scholar 

  17. Laurs, R. M. & Lynn, J. Seasonal migration of North Pacific albacore, Thunnus alalunga, into North American coastal waters: Distribution, relative abundance, and association with Transition Zone waters. Fish. Bull. (Wash D C). 75 (4), 795–822 (1977).

    Google Scholar 

  18. Muhling, B. A. et al. Risk and Reward in Foraging Migrations of North Pacific Albacore Determined From Estimates of Energy Intake and Movement Costs. Front. Mar. Sci. 9 https://doi.org/10.3389/fmars.2022.730428 (2022).

  19. Arostegui, M. C. et al. A shallow scattering layer structures the energy seascape of an open ocean predator. Sci. Adv. 9 (40), eadi8200. https://doi.org/10.1126/sciadv.adi8200 (2023).

    Google Scholar 

  20. Nickels, C. F., Portner, E. J., Snodgrass, O., Muhling, B. & Dewar, H. Juvenile Albacore tuna (Thunnus alalunga) foraging ecology varies with environmental conditions in the California Current Large Marine Ecosystem. Fish. Oceanogr. 32 (5), 431–447. https://doi.org/10.1111/fog.12638 (2023).

    Google Scholar 

  21. de Boyer Montégut, C., Madec, G., Fischer, A. S., Lazar, A. & Iudicone, D. Mixed layer depth over the global ocean: An examination of profile data and a profile-based climatology. J. Geophys. Research: Oceans. 109 (C12). https://doi.org/10.1029/2004JC002378 (2004).

  22. Williams, A. J. et al. Vertical behavior and diet of albacore tuna (Thunnus alalunga) vary with latitude in the South Pacific Ocean. Deep Sea Res. Part II. 113, 154–169. https://doi.org/10.1016/j.dsr2.2014.03.010 (2015).

    Google Scholar 

  23. Snyder, S. M. Navigating a seascape: Physiological and environmental motivations behind juvenile North Pacific albacore movement patterns [UC San Diego]. (2016). https://escholarship.org/uc/item/46m1g0sm

  24. Muhling, B. et al. (n.d.). Dynamic Habitat Use of Albacore and their Primary Prey Species in the California Current System. Retrieved July 18, from (2025). https://repository.library.noaa.gov/view/noaa/37600

  25. Pinkas, L., Oliphant, M. S. & Iverson, I. L. K. Fish Bulletin 152. Food Habits of Albacore, Bluefin Tuna, and Bonito In California Waters. (1970). https://escholarship.org/uc/item/7t5868rd

  26. Glaser, S. M. Interdecadal variability in predator–prey interactions of juvenile North Pacific albacore in the California Current System. Mar. Ecol. Prog. Ser. 414, 209–221. https://doi.org/10.3354/meps08723 (2010).

    Google Scholar 

  27. IPCC. in Climate Change 2023: Synthesis Report. Contribution of Working Groups I, II and III to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change [Core Writing Team. 35–115 (eds Lee, H. & Romero, J.) (IPCC, 2023). https://doi.org/10.59327/IPCC/AR6-9789291691647

  28. Jang, C. J., Park, J., Park, T. & Yoo, S. Response of the ocean mixed layer depth to global warming and its impact on primary production: A case for the North Pacific Ocean. ICES J. Mar. Sci. 68 (6), 996–1007. https://doi.org/10.1093/icesjms/fsr064 (2011).

    Google Scholar 

  29. Gilman, E., Allain, V., Collette, B. B., Hampton, J. & Lehodey, P. (n.d.). Effects of Ocean Warming on Pelagic Tunas, a Review. Retrieved July 18, from (2025). https://repository.si.edu/items/d400dbe1-da66-41ad-bf9b-abd811e83792

  30. Chust, G. et al. Earlier migration and distribution changes of albacore in the Northeast Atlantic. Fish. Oceanogr. 28 (5), 505–516. https://doi.org/10.1111/fog.12427 (2019).

    Google Scholar 

  31. Dufour, F., Arrizabalaga, H., Irigoien, X. & Santiago, J. Climate impacts on albacore and bluefin tunas migrations phenology and spatial distribution. Prog. Oceanogr. 86 (1), 283–290. https://doi.org/10.1016/j.pocean.2010.04.007 (2010).

    Google Scholar 

  32. Senina, I. et al. and Impact of climate change on tropical Pacific tuna and their fisheries in Pacific Islands waters and high seas areas. (2018). https://www.spc.int/DigitalLibrary/Doc/FAME/Meetings/WCPFC/SC14/SC14_EB_WP_01_Pacific_Tuna_Climate_Change.pdf

  33. Smith, J. A. et al. Projecting climate change impacts from physics to fisheries: A view from three California Current fisheries. Prog. Oceanogr. 211, 102973. https://doi.org/10.1016/j.pocean.2023.102973 (2023).

    Google Scholar 

  34. Erauskin-Extramiana, M. et al. Implications for the global tuna fishing industry of climate change-driven alterations in productivity and body sizes. Glob. Planet Change. 222, 104055. https://doi.org/10.1016/j.gloplacha.2023.104055 (2023).

    Google Scholar 

  35. Muhling, B. et al. Climate change impacts to foraging seascapes for a highly migratory top predator. Mov. Ecol. 13 (1), 33. https://doi.org/10.1186/s40462-025-00558-1 (2025).

    Google Scholar 

  36. Chang, Y. J., Hsu, J., Lai, P. K., Lan, K. W. & Tsai, W. P. Evaluation of the Impacts of Climate Change on Albacore Distribution in the South Pacific Ocean by Using Ensemble Forecast. Front. Mar. Sci. 8 https://doi.org/10.3389/fmars.2021.731950 (2021).

  37. Lezama-Ochoa, N. et al. Divergent responses of highly migratory species to climate change in the California Current. Divers. Distrib. 30 (2), e13800. https://doi.org/10.1111/ddi.13800 (2024).

    Google Scholar 

  38. Derville, S., Torres, L. G., Iovan, C. & Garrigue, C. Finding the right fit: Comparative cetacean distribution models using multiple data sources and statistical approaches. Divers. Distrib. 24 (11), 1657–1673. https://doi.org/10.1111/ddi.12782 (2018).

    Google Scholar 

  39. Muhling, B. A. et al. Predictability of Species Distributions Deteriorates Under Novel Environmental Conditions in the California Current System. Front. Mar. Sci. 7 https://doi.org/10.3389/fmars.2020.00589 (2020).

  40. Sirén, J., Somervuo, P. & Ovaskainen, O. Agent-based versus correlative models of species distributions: Evaluation of predictive performance with real and simulated data. Methods Ecol. Evol. 16 (6), 1295–1307. https://doi.org/10.1111/2041-210X.70016 (2025).

    Google Scholar 

  41. Yates, K. L. et al. Outstanding Challenges in the Transferability of Ecological Models. Trends Ecol. Evol. 33 (10), 790–802. https://doi.org/10.1016/j.tree.2018.08.001 (2018).

    Google Scholar 

  42. Zurell, D., Jeltsch, F., Dormann, C. F. & Schroder, B. Static species distribution models in dynamically changing systems: How good can predictions really be? Ecography 32, 733–744 (2009).

    Google Scholar 

  43. Fiechter, J., Huckstadt, L. A., Rose, K. A. & Costa, D. P. A fully coupled ecosystem model to predict the foraging ecology of apex predators in the California Current. (2016). https://doi.org/10.3354/meps11849

  44. Dodson, S., Abrahms, B., Bograd, S. J., Fiechter, J. & Hazen, E. L. Disentangling the biotic and abiotic drivers of emergent migratory behavior using individual-based models. Ecol. Model. 432, 109225. https://doi.org/10.1016/j.ecolmodel.2020.109225 (2020).

    Google Scholar 

  45. Scutt Phillips, J. et al. An individual-based model of skipjack tuna (Katsuwonus pelamis) movement in the tropical Pacific ocean. Prog. Oceanogr. 164, 63–74. https://doi.org/10.1016/j.pocean.2018.04.007 (2018).

    Google Scholar 

  46. Deutsch, C. et al. Biogeochemical variability in the California Current System. bioRxiv 2020.02.10.942565 https://doi.org/10.1101/2020.02.10.942565 (2021).

  47. Arostegui, M. C., Gaube, P., Woodworth-Jefcoats, P. A., Kobayashi, D. R. & Braun, C. D. Anticyclonic eddies aggregate pelagic predators in a subtropical gyre. Nature 609 (7927), 535–540. https://doi.org/10.1038/s41586-022-05162-6 (2022).

    Google Scholar 

  48. Druon, J. N. et al. Global-Scale Environmental Niche and Habitat of Blue Shark (Prionace glauca) by Size and Sex: A Pivotal Step to Improving Stock Management. Frontiers in Marine Science, 9. (2022). https://doi.org/10.3389/fmars.2022.828412

  49. Vaux, F., Bohn, S., Hyde, J. R. & O’Malley, K. G. Adaptive markers distinguish North and South Pacific Albacore amid low population differentiation. Evol. Appl. 14 (5), 1343–1364. https://doi.org/10.1111/eva.13202 (2021).

    Google Scholar 

  50. Phillips, A. J., Ciannelli, L., Brodeur, R. D., Pearcy, W. G. & Childers, J. Spatio-temporal associations of albacore CPUEs in the Northeastern Pacific with regional SST and climate environmental variables. ICES J. Mar. Sci. 71 (7), 1717–1727. https://doi.org/10.1093/icesjms/fst238 (2014).

    Google Scholar 

  51. Athanase, M., Sánchez-Benítez, A., Goessling, H. F., Pithan, F. & Jung, T. Projected amplification of summer marine heatwaves in a warming Northeast Pacific Ocean. Commun. Earth Environ. 5 (1), 53. https://doi.org/10.1038/s43247-024-01212-1 (2024).

    Google Scholar 

  52. Sun, W. et al. Marine Heatwaves/Cold-Spells Associated With Mixed Layer Depth Variation Globally. Geophys. Res. Lett. 51 (24), e2024GL112325. https://doi.org/10.1029/2024GL112325 (2024).

    Google Scholar 

  53. Lennox, R. J. et al. One hundred pressing questions on the future of global fish migration science, conservation, and policy. Front. Ecol. Evol. 7 https://doi.org/10.3389/fevo.2019.00286 (2019).

  54. Robinson, A. et al. Vieira dos Santos, M. E. Travelling through a warming world: Climate change and migratory species. Endangered Species Research, 7, 87–99. (2009). https://doi.org/10.3354/esr00095

  55. Lam, C. H., Nielsen, A. & Sibert, J. R. Improving light and temperature based geolocation by unscented Kalman filtering. Fish. Res. 91 (1), 15–25. https://doi.org/10.1016/j.fishres.2007.11.002 (2008).

    Google Scholar 

  56. Nielsen, A., Sibert, J. R., Ancheta, J., Galuardi, B. & Lam, C. H. ukfsst: Kalman Filter tracking including Sea Surface Temperature. R package version 0.3. (2012).

  57. Reynolds, R. W., Rayner, N. A., Smith, T. M., Stokes, D. C. & Wang, W. An Improved In Situ and Satellite SST Analysis for Climate. (2002). https://journals.ametsoc.org/view/journals/clim/15/13/1520-0442_2002_015_1609_aiisas_2.0.co_2.xml

  58. Galuardi, B. et al. Complex migration routes of Atlantic bluefin tuna (Thunnus thynnus) question current population structure paradigm. Can. J. Fish. Aquat. Sci. 67 (6), 966–976. https://doi.org/10.1139/F10-033 (2010).

    Google Scholar 

  59. Hill, R. D. & Braun, M. J. Geolocation by light level. Reviews: Methods Technol. Fish. Biology Fisheries. 315–330. https://doi.org/10.1007/978-94-017-1402-0_17 (2001).

  60. GLORYS12V1. E.U. Copernicus Marine Service Information (CMEMS). Marine Data Store (MDS). DOI: 10.48670/moi-00021 (Accessed on 07- (2023).

  61. Christian, J. R. & Holmes, J. Changes in albacore tuna habitat in the northeast Pacific Ocean under anthropogenic warming. Fish. Oceanogr. 25 (5), 544–554. https://doi.org/10.1111/fog.12171 (2016).

    Google Scholar 

  62. Stocker, M., Stiff, H., Shaw, W. & Argue, A. W. The Canadian Albacore Tuna Catch and Effort Relational Database. Can. Tech. Rep. Fish. Aquat. Sci. 2701, vi– (2007).

    Google Scholar 

  63. Benhamou, S., Sauvé, J. P. & Bovet, P. Spatial memory in large scale movements: Efficiency and limitation of the egocentric coding process. J. Theor. Biol. 145 (1), 1–12. https://doi.org/10.1016/S0022-5193(05)80531-4 (1990).

    Google Scholar 

  64. Scott, J. D., Alexander, M. A., Murray, D. R., Swales, D. & Eischeid, J. The Climate Change Web Portal: A System to Access and Display Climate and Earth System Model Output from the CMIP5 Archive. (2016). https://doi.org/10.1175/BAMS-D-15-00035.1

Download references

Acknowledgements

This research was conducted as part of the Brown University Ocean, Climate, and Ecosystem Data Science Internship Program (https://www.ocean.brown.edu/oce-internship). R. Gasbarro provided helpful comments to an earlier draft of the manuscript. We thank the captains and crew of all vessels which released and recaptured albacore, including commercial and sport fishermen. We thank the Albacore Research Foundation for their support of research using the albacore tagging program data, as well as John Childers and Suzy Kohin, who were instrumental in developing the program.

Funding

This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.

Author information

Authors and Affiliations

Authors

Contributions

LAD, CE, and CD contributed to all aspects of this study and share first authorship. EDL, BAM, and SSK contributed to the study design. EDL, LAD, CE and CD led data analysis and visualization. EDL, BAM and SSK advised on data analysis and interpretation of results. LAD led the writing of the manuscript with CE and CD and contributions from EDL, BAM, and SSK.

Corresponding author

Correspondence to
Lorenzo A. Davidson.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary Material 1 (download DOCX )

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Cite this article

Davidson, L.A., Erdozain, C.M., Drake, C.R. et al. An individual-based model of North Pacific albacore tuna seasonal migratory behaviour and climate sensitivity.
Sci Rep (2026). https://doi.org/10.1038/s41598-026-46968-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1038/s41598-026-46968-y

Keywords

  • Albacore tuna
  • Individual-based model
  • Mixed layer depth
  • Migration phenology


Source: Ecology - nature.com

Comparative environmental and economic assessment of greenhouse cucumber and opuntia ficus-indica cultivation in arid regions

Asymmetric biparental and inefficient horizontal transmission of paralysis-causing sigmavirus in Queensland fruit fly

Back to Top