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Vertical climate velocity adds a critical dimension to species shifts

Abstract

Climate responses of marine organisms differ from those on land as marine species have the flexibility to move vertically. While horizontal climate velocity has been used to predict poleward range shifts, many species are not moving as expected. Incorporating shifts in depth, which have received less attention, may better explain climate responses of marine organisms. Here we assess vertical and horizontal climate velocities across 63 global large marine ecosystems and find that 77% of vertical climate velocities are negative, reflecting isotherm deepening. Vertical climate velocity is 10,000 times smaller than horizontal climate velocity, allowing organisms to maintain constant temperatures by shifting metres in depth rather than kilometres horizontally. Within three key large marine ecosystems, we find more species shifts are explained by vertical than by horizontal climate velocity. Together, our findings have implications for understanding species adaptation to change and for future accessibility of marine resources.

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Fig. 1: Negative VCV indicates deepening isotherms.
Fig. 2: Across global LMEs, the highest HCV and more negative VCV values occurred at lower latitudes.
Fig. 3: HCV and VCV for three key LMEs show heterogeneity associated with regional warming and stratification patterns.
Fig. 4: VCVs are in line with species shifts in depth in three key LMEs.
Fig. 5: Simulated species shifts vary widely under different combinations of VCVs and HCVs.
Fig. 6: During 2019 the majority of fisheries landings occurred where median VCV was between −1 and 0 m yr−1.

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Data availability

All data are publicly available. GLORYS12 version 1 monthly reanalysis is available at https://data.marine.copernicus.eu/product/GLOBAL_MULTIYEAR_PHY_001_030/description. Trawl data from the FishGlob project can be accessed via Github at https://github.com/AquaAuma/FishGlob_data. Fisheries catch data from 2019 are available at http://www.seaaroundus.org/data/#/lme.

Code availability

The Python code used to calculate vertical and horizontal climate velocities and species shifts is available via GitHub at https://github.com/lagruenburg/Vertical_Climate_Velocity (ref. 65).

References

  1. Parmesan, C. et al. Empirical perspectives on species borders: from traditional biogeography to global change. Oikos 108, 58–75 (2005).

    Article  Google Scholar 

  2. Parmesan, C. & Yohe, G. A globally coherent fingerprint of climate change impacts across natural systems. Nature 421, 37–42 (2003).

    Article  CAS  Google Scholar 

  3. Dulvy, N. K. et al. Climate change and deepening of the North Sea fish assemblage: a biotic indicator of warming seas. J. Appl. Ecol. 45, 1029–1039 (2008).

    Article  Google Scholar 

  4. Poloczanska, E. S. et al. Global imprint of climate change on marine life. Nat. Clim. Change 3, 919–925 (2013).

    Article  Google Scholar 

  5. Perry, A. L., Low, P. J., Ellis, J. R. & Reynolds, J. D. Climate change and distribution shifts in marine fishes. Science 308, 1912–1915 (2005).

    Article  CAS  Google Scholar 

  6. Pecl, G. T. et al. Biodiversity redistribution under climate change: impacts on ecosystems and human well-being. Science 355, eaai9214 (2017).

    Article  Google Scholar 

  7. Loarie, S. R. et al. The velocity of climate change. Nature 462, 1052–1055 (2009).

    Article  CAS  Google Scholar 

  8. Burrows, M. T. et al. The pace of shifting climate in marine and terrestrial ecosystems. Science 334, 652–655 (2011).

    Article  CAS  Google Scholar 

  9. Pinsky, M. L., Worm, B., Fogarty, M. J., Sarmiento, J. L. & Levin, S. A. Marine taxa track local climate velocities. Science 341, 1239–1242 (2013).

    Article  CAS  Google Scholar 

  10. Sunday, J. M. et al. Species traits and climate velocity explain geographic range shifts in an ocean-warming hotspot. Ecol. Lett. 18, 944–953 (2015).

    Article  Google Scholar 

  11. Lenoir, J. et al. Species better track climate warming in the oceans than on land. Nat. Ecol. Evol. 4, 1044–1059 (2020).

    Article  Google Scholar 

  12. Lenoir, J. & Svenning, J.-C. Climate-related range shifts—a global multidimensional synthesis and new research directions. Ecography 38, 15–28 (2015).

    Article  Google Scholar 

  13. VanDerWal, J. et al. Focus on poleward shifts in species’ distribution underestimates the fingerprint of climate change. Nat. Clim. Change 3, 239–243 (2013).

    Article  Google Scholar 

  14. Moritz, C. et al. Impact of a century of climate change on small-mammal communities in Yosemite National Park, USA. Science 322, 261–264 (2008).

    Article  CAS  Google Scholar 

  15. Lenoir, J., Gégout, J. C., Marquet, P. A., De Ruffray, P. & Brisse, H. A significant upward shift in plant species optimum elevation during the 20th century. Science 320, 1768–1771 (2008).

    Article  CAS  Google Scholar 

  16. Chen, I.-C., Hill, J. K., Ohlemüller, R., Roy, D. B. & Thomas, C. D. Rapid range shifts of species associated with high levels of climate warming. Science 333, 1024–1026 (2011).

    Article  CAS  Google Scholar 

  17. Woolway, R. I. & Maberly, S. C. Climate velocity in inland standing waters. Nat. Clim. Change 10, 1124–1129 (2020).

    Article  Google Scholar 

  18. Thorne, L. H. & Nye, J. A. Trait-mediated shifts and climate velocity decouple an endothermic marine predator and its ectothermic prey. Sci. Rep. 11, 18507 (2021).

    Article  CAS  Google Scholar 

  19. Burrows, M. T. et al. Ocean community warming responses explained by thermal affinities and temperature gradients. Nat. Clim. Change 9, 959–963 (2019).

    Article  Google Scholar 

  20. Engelhard, G. H., Righton, D. A. & Pinnegar, J. K. Climate change and fishing: a century of shifting distribution in North Sea cod. Glob. Change Biol. 20, 2473–2483 (2014).

    Article  Google Scholar 

  21. Santana-Falcón, Y. & Séférian, R. Climate change impacts the vertical structure of marine ecosystem thermal ranges. Nat. Clim. Change 12, 935–942 (2022).

    Article  Google Scholar 

  22. Chaikin, S., Dubiner, S., Belmaker, J. & MacNeil, A. Cold‐water species deepen to escape warm water temperatures. Glob. Ecol. Biogeogr. 31, 75–88 (2022).

    Article  Google Scholar 

  23. Meyer‐Gutbrod, E. et al. Moving on up: vertical distribution shifts in rocky reef fish species during climate‐driven decline in dissolved oxygen from 1995 to 2009. Glob. Change Biol. 27, 6280–6293 (2021).

    Article  Google Scholar 

  24. Brito-Morales, I. et al. Climate velocity reveals increasing exposure of deep-ocean biodiversity to future warming. Nat. Clim. Change 10, 576–581 (2020).

    Article  CAS  Google Scholar 

  25. Jorda, G. et al. Ocean warming compresses the three-dimensional habitat of marine life. Nat. Ecol. Evol. 4, 109–114 (2019).

    Article  Google Scholar 

  26. Costello, M. J. & Chaudhary, C. Marine biodiversity, biogeography, deep-sea gradients, and conservation. Curr. Biol. 27, R511–R527 (2017).

    Article  CAS  Google Scholar 

  27. Levitus, S. et al. Anthropogenic warming of earth’s climate system. Science 292, 267–270 (2001).

    Article  CAS  Google Scholar 

  28. Lyman, J. M. et al. Robust warming of the global upper ocean. Nature 465, 334–337 (2010).

    Article  CAS  Google Scholar 

  29. Domingues, C. M. et al. Improved estimates of upper-ocean warming and multi-decadal sea-level rise. Nature 453, 1090–1093 (2008).

    Article  CAS  Google Scholar 

  30. Durack, P. J., Gleckler, P. J., Landerer, F. W. & Taylor, K. E. Quantifying underestimates of long-term upper-ocean warming. Nat. Clim. Change 4, 999–1005 (2014).

    Article  Google Scholar 

  31. Stock, C. A. et al. Reconciling fisheries catch and ocean productivity. Proc. Natl Acad. Sci. USA 114, E1441–E1449 (2017).

    Article  CAS  Google Scholar 

  32. Belkin, I. M. Rapid warming of large marine ecosystems. Prog. Oceanogr. 81, 207–213 (2009).

    Article  Google Scholar 

  33. Pershing, A. J. et al. Slow adaptation in the face of rapid warming leads to collapse of the Gulf of Maine cod fishery. Science 350, 809–812 (2015).

    Article  CAS  Google Scholar 

  34. Sherman, K., Belkin, I. M., Friedland, K. D., O’Reilly, J. & Hyde, K. Accelerated warming and emergent trends in fisheries biomass yields of the world’s large marine ecosystems. AMBIO J. Hum. Environ. 38, 215–224 (2009).

    Article  Google Scholar 

  35. Global Ocean Physics Reanalysis, Mercator Ocean International (European Union–Copernicus Marine Service, 2018); https://doi.org/10.48670/MOI-00021

  36. Stevens, G. C. The latitudinal gradient in geographical range: how so many species coexist in the tropics. Am. Nat. 133, 240–256 (1989).

    Article  Google Scholar 

  37. Sunday, J. M., Bates, A. E. & Dulvy, N. K. Global analysis of thermal tolerance and latitude in ectotherms. Proc. R. Soc. B Biol. Sci. 278, 1823–1830 (2011).

    Article  Google Scholar 

  38. Smale, D. A. et al. Marine heatwaves threaten global biodiversity and the provision of ecosystem services. Nat. Clim. Change 9, 306–312 (2019).

    Article  Google Scholar 

  39. Özsoy, E. & Ünlüata, Ü. Oceanography of the Black Sea: a review of some recent results. Earth Sci. Rev. 42, 231–272 (1997).

    Article  Google Scholar 

  40. Robinson, M. K. The Physical Oceanography of the Gulf of Thailand, Naga Expedition; Bathythermograph (BT) Temperature Observations in the Timor Sea, Naga Expedition, Cruise S11 (Scripps Institution of Oceanography, 1974).

  41. Zeng, L. & Wang, D. Seasonal variations in the barrier layer in the South China Sea: characteristics, mechanisms and impact of warming. Clim. Dyn. 48, 1911–1930 (2017).

    Article  Google Scholar 

  42. Yanagi, T., Sachoemar, S. I., Takao, T. & Fujiwara, S. Seasonal variation of stratification in the Gulf of Thailand. J. Oceanogr. 57, 461–470 (2001).

    Article  CAS  Google Scholar 

  43. Rudels, B. & Carmack, E. Arctic ocean water mass structure and circulation. Oceanography https://doi.org/10.5670/oceanog.2022.116 (2022).

  44. Stabeno, P. J. & Bell, S. W. Extreme conditions in the Bering Sea (2017–2018): record‐breaking low sea‐ice extent. Geophys. Res. Lett. 46, 8952–8959 (2019).

    Article  Google Scholar 

  45. Spies, I. et al. Genetic evidence of a northward range expansion in the eastern Bering Sea stock of Pacific cod. Evol. Appl. 13, 362–375 (2020).

    Article  CAS  Google Scholar 

  46. Wang, Z., Boyer, T., Reagan, J. & Hogan, P. Upper-oceanic warming in the Gulf of Mexico between 1950 and 2020. J. Clim. 36, 2721–2734 (2023).

    Article  Google Scholar 

  47. Gangopadhyay, A. et al. A census of the warm‐core rings of the Gulf Stream: 1980–2017. J. Geophys. Res. Oceans 125, e2019JC016033 (2020).

    Article  Google Scholar 

  48. Gonçalves Neto, A., Langan, J. A. & Palter, J. B. Changes in the Gulf Stream preceded rapid warming of the Northwest Atlantic Shelf. Commun. Earth Environ. 2, 74 (2021).

    Article  Google Scholar 

  49. Kleisner, K. M. et al. The effects of sub-regional climate velocity on the distribution and spatial extent of marine species assemblages. PLoS ONE 11, e0149220 (2016).

    Article  Google Scholar 

  50. Houghton, R. W., Schlitz, R., Beardsley, R. C., Butman, B. & Chamberlin, J. L. The middle atlantic bight cold pool: evolution of the temperature structure during summer 1979. J. Phys. Oceanogr. 12, 1019–1029 (1982).

    Article  Google Scholar 

  51. Ojea, E., Lester, S. E. & Salgueiro-Otero, D. Adaptation of fishing communities to climate-driven shifts in target species. One Earth 2, 544–556 (2020).

    Article  Google Scholar 

  52. Dubik, B. A. et al. Governing fisheries in the face of change: social responses to long-term geographic shifts in a U.S. fishery. Mar. Policy 99, 243–251 (2019).

    Article  Google Scholar 

  53. Powell, F., Levine, A. & Ordonez-Gauger, L. Climate adaptation in the market squid fishery: fishermen responses to past variability associated with El Niño Southern Oscillation cycles inform our understanding of adaptive capacity in the face of future climate change. Clim. Change 173, 1 (2022).

    Article  Google Scholar 

  54. Pinsky, M. L. et al. Fish and fisheries in hot water: what is happening and how do we adapt? Popul. Ecol. 63, 17–26 (2021).

    Article  Google Scholar 

  55. Ljungström, G., Langbehn, T. J. & Jørgensen, C. Light and energetics at seasonal extremes limit poleward range shifts. Nat. Clim. Change 11, 530–536 (2021).

    Article  Google Scholar 

  56. Muniz, P., Venturini, N., Brugnoli, E., Gutiérrez, J. M. & Acuña, A. in World Seas: An Environmental Evaluation 2nd ed. (ed. Sheppard, C.) 703–724 (Elsevier, 2019); https://doi.org/10.1016/B978-0-12-805068-2.00036-X

  57. Voluntary Guidelines for Securing Sustainable Small-Scale Fisheries in the Context of Food Security and Poverty Eradication (FAO, 2015).

  58. Hamann, A., Roberts, D. R., Barber, Q. E., Carroll, C. & Nielsen, S. E. Velocity of climate change algorithms for guiding conservation and management. Glob. Change Biol. 21, 997–1004 (2015).

    Article  Google Scholar 

  59. Lellouche, J.-M. et al. The Copernicus Global 1/12° Ocean and Sea Ice GLORYS12 Reanalysis. Front. Earth Sci. 9, 698876 (2021).

    Article  Google Scholar 

  60. De Souza, J. M. A. C., Couto, P., Soutelino, R. & Roughan, M. Evaluation of four global ocean reanalysis products for New Zealand waters—a guide for regional ocean modelling. N.Z. J. Mar. Freshw. Res. 55, 132–155 (2021).

    Article  Google Scholar 

  61. Amaya, D. J., Alexander, M. A., Scott, J. D. & Jacox, M. G. An evaluation of high-resolution ocean reanalyses in the California current system. Prog. Oceanogr. 210, 102951 (2023).

    Article  Google Scholar 

  62. Verezemskaya, P. et al. Assessing eddying (1/12°) ocean reanalysis GLORYS12 using the 14-yr instrumental record from 59.5° N section in the Atlantic. J. Geophys. Res. Oceans 126, e2020JC016317 (2021).

    Article  Google Scholar 

  63. Maureaud, A. A. et al. FISHGLOB_data: an integrated dataset of fish biodiversity sampled with scientific bottom-trawl surveys. Sci. Data 11, 24 (2024).

    Article  Google Scholar 

  64. Pauly, D., Zeller, D. & Palomares, M. L. D. Concepts, design and data. Sea Around Us https://seaaroundus.org (2020).

  65. Gruenburg, L. lagruenburg/Vertical_Climate_Velocity: vertical climate velocity initial release. Zenodo https://doi.org/10.5281/ZENODO.14548102 (2024).

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Acknowledgements

Support for this work was provided by the New York State Environmental Protection Fund Ocean and Great Lakes Program, New York State Department of Environmental Conservation.

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L.T. and J.N. secured funding for the project. All authors designed the climate velocity analysis. L.K.G., L.T. and J.N. designed the species shift analysis. L.K.G. preformed the analyses. All authors prepared the manuscript.

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Correspondence to Laura K. Gruenburg.

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Nature Climate Change thanks Isaac Brito Morales, Yeray Santana-Falcón, and the other, anonymous, reviewers for their contribution to the peer review of this work.

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Extended data

Extended Data Fig. 1 Vertical and horizontal temperature gradients in each Large Marine Ecosystem (LME).

Half violin and boxplots for vertical temperature gradient (left) and horizontal temperature gradient at the surface (right) within each LME. LME names and associated number are on the leftmost y-axis. LMEs are grouped by their geographic region with tropical LMEs at the top in red followed below by subtropical in yellow, temperate in brown, subarctic in light blue and arctic in dark blue. In both vertical and horizontal temperature gradient plots a dashed vertical line shows 0 Cm−1 (Ckm−1).

Extended Data Fig. 2 Full-depth and surface only temperature trends in each Large Marine Ecosystem (LME).

Half violin and boxplots for temperature trend in the subsurface (left) and surface temperature trend (right) within each LME. LME names and associated number are on the leftmost y-axis. LMEs are grouped by their geographic region with tropical LMEs at the top in red followed below by subtropical in yellow, temperate in brown, subarctic in light blue and arctic in dark blue. In both vertical and horizontal climate velocity plots a dashed vertical line shows 0 °Cyr−1.

Extended Data Fig. 3 In the Gulf of Mexico many species shifted longitudinally toward the east.

Species movements in the U.S. Gulf of Mexico from trawl survey data post 1992. The colors indicate the mean sea surface temperature during the fall (averaged September, October, November). Cooler temperatures are present in the northern part of the Gulf along the US coast, and also in the eastern part of the Gulf along the western Florida coast. Here we show only species whose movement was farther east than the zonal component of horizontal climate velocity would suggest. Black diamonds represent the biomass weighted mean latitude and longitude of a single species at the earliest point it appears in the trawl data post 1992, we call this the ‘starting location’. The grey lines show simplified pathways taken by these species as straight lines connecting all weighted latitude longitude locations each year. The ‘x’, triangle, and circle markers show the last biomass weighted mean location of the species (the most recent year in which that species was present); we term this the ending location. The ‘x’ indicates that there was no significant linear temporal trend in depth for this species. The orange circle indicates the species moved in agreement with vertical climate velocity, the pink ‘down’ triangle indicates movement deeper than vertical climate velocity would suggest, and the green ‘up’ triangle indicates the species moved shallower than vertical climate velocity would suggest. Many of the species started out along the Texas and Louisiana coasts and migrated toward the west Florida coast.

Extended Data Fig. 4 Many species shifted longitudinally, most notably in the Gulf of Mexico.

Climate velocities (boxplots) for the Northeast U.S. (NEUS), Gulf of Mexico (G of Mex), and East Bering Sea (E Bering S) relative to the rate of statistically significant distributional shifts for fish and invertebrate species (points). Center lines within the box plots show median values, box limits show the upper and lower quartile, the upper whisker shows the upper quartile plus 1.5 times the interquartile range, and the lower whisker shows the lower quartile minus 1.5 times the interquartile range. Outliers are omitted from the boxplots. Points occurring within the whiskers of the box plot show movement as expected based on climate velocity, while those occurring above or below the whiskers of the boxplots show movement that is farther east or west than expected based on horizontal climate velocity (HCV). Longitudinal component of HCV relative to east/west movement. The dots are colored to show rates of movement that are farther east, farther west, or in agreement with climate velocity. Axis limits in panel a) are restricted to better show overlap between climate velocity boxplots and species rates of movement. In b) axis limits allow all species to be shown.

Extended Data Fig. 5 Climate velocities and species shifts with outliers shown.

Climate velocities (boxplots) for the Northeast U.S. (NEUS), Gulf of Mexico (G of Mex), and East Bering Sea (E Bering S) relative to the rate of statistically significant distributional shifts for fish and invertebrate species (points), as in Fig. 4. Here axis limits allow outlier species to be shown. Center lines within the box plots show median values, box limits show the upper and lower quartile, the upper whisker shows the upper quartile plus 1.5 times the interquartile range, and the lower whisker shows the lower quartile minus 1.5 times the interquartile range. Outliers are omitted from the boxplots. Points occurring within the whiskers of the box plot show movement as expected based on climate velocity, while those occurring above or below the whiskers of the boxplots show movement that is further north (shallower) or south (deeper), respectively, than expected based on horizontal climate velocity (HCV) or vertical climate velocity (VCV). a) Latitudinal component of HCV relative to north/south movement. The dots are colored to show rates of movement that are farther north, farther south, or in agreement with climate velocity. b) VCV relative to movement in depth. The dots are colored to show rates of vertical movement that indicate deeper than, shallower than, or in agreement with climate velocity. c) VCV relative to movement in depth for species that did not show any significant horizontal (latitudinal or longitudinal) shifts. Colors as in b).

Extended Data Table 1 The resulting sign of climate velocity under all combinations of spatial gradients and temporal trends of temperature
Extended Data Table 2 All species significant and non-significant shifts in three dimensions
Extended Data Table 3 Species that reached a border of the Large Marine Ecosystem during the simulation

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Supplementary Figs. 1 and 2.

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Gruenburg, L.K., Nye, J., Lwiza, K. et al. Vertical climate velocity adds a critical dimension to species shifts. Nat. Clim. Chang. 15, 656–664 (2025). https://doi.org/10.1038/s41558-025-02300-6

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