Volume 25, Issue 2
PRIMARY RESEARCH ARTICLE

Climate change resilience of a globally important sea turtle nesting population

Ana R. Patrício

Corresponding Author

Centre for Ecology and Conservation, University of Exeter, Penryn, UK

MARE – Marine and Environmental Sciences Centre, ISPA – Instituto Universitário, Lisbon, Portugal

Correspondence

Ana Rita Patrício, Centre for Ecology and Conservation, University of Exeter, Penryn, UK.

Email: R.Patricio@exeter.ac.uk

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Miguel R. Varela

Centre for Ecology and Conservation, University of Exeter, Penryn, UK

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Castro Barbosa

Institute of Biodiversity and Protected Areas of Guinea‐Bissau, Bissau, Guinea‐Bissau

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Annette C. Broderick

Centre for Ecology and Conservation, University of Exeter, Penryn, UK

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Paulo Catry

MARE – Marine and Environmental Sciences Centre, ISPA – Instituto Universitário, Lisbon, Portugal

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Lucy A. Hawkes

Centre for Ecology and Conservation, University of Exeter, Penryn, UK

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Aissa Regalla

Institute of Biodiversity and Protected Areas of Guinea‐Bissau, Bissau, Guinea‐Bissau

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Brendan J. Godley

Centre for Ecology and Conservation, University of Exeter, Penryn, UK

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First published: 19 December 2018
Citations: 11

Abstract

Few studies have looked into climate change resilience of populations of wild animals. We use a model higher vertebrate, the green sea turtle, as its life history is fundamentally affected by climatic conditions, including temperature‐dependent sex determination and obligate use of beaches subject to sea level rise (SLR). We use empirical data from a globally important population in West Africa to assess resistance to climate change within a quantitative framework. We project 200 years of primary sex ratios (1900–2100) and create a digital elevation model of the nesting beach to estimate impacts of projected SLR. Primary sex ratio is currently almost balanced, with 52% of hatchlings produced being female. Under IPCC models, we predict: (a) an increase in the proportion of females by 2100 to 76%–93%, but cooler temperatures, both at the end of the nesting season and in shaded areas, will guarantee male hatchling production; (b) IPCC SLR scenarios will lead to 33.4%–43.0% loss of the current nesting area; (c) climate change will contribute to population growth through population feminization, with 32%–64% more nesting females expected by 2120; (d) as incubation temperatures approach lethal levels, however, the population will cease growing and start to decline. Taken together with other factors (degree of foraging plasticity, rookery size and trajectory, and prevailing threats), this nesting population should resist climate change until 2100, and the availability of spatial and temporal microrefugia indicates potential for resilience to predicted impacts, through the evolution of nest site selection or changes in nesting phenology. This represents the most comprehensive assessment to date of climate change resilience of a marine reptile using the most up‐to‐date IPCC models, appraising the impacts of temperature and SLR, integrated with additional ecological and demographic parameters. We suggest this as a framework for other populations, species and taxa.

Number of times cited according to CrossRef: 11

  • Are trends in Olive Ridley sea turtle (Lepidochelys olivacea) nesting abundance affected by El Niño Southern Oscillation (ENSO) variability? Sixteen years of monitoring on the Pacific coast of northern Central America, Global Ecology and Conservation, 10.1016/j.gecco.2020.e01339, (e01339), (2020).
  • Nesting failure of sea turtles in Ecuador - causes of the loss of sea turtle nests: the role of the tide, Journal of Coastal Conservation, 10.1007/s11852-020-00775-3, 24, 5, (2020).
  • Potential adaptability of marine turtles to climate change may be hindered by coastal development in the USA, Regional Environmental Change, 10.1007/s10113-020-01689-4, 20, 3, (2020).
  • Taking Stock of Climate Change Induced Sea Level Rise across the West African Coast, Environmental Claims Journal, 10.1080/10406026.2020.1847873, (1-14), (2020).
  • Warmer incubation temperature influences sea turtle survival and nullifies the benefit of a female-biased sex ratio, Climatic Change, 10.1007/s10584-020-02933-w, (2020).
  • Climate Change and Green Sea Turtle Sex Ratio—Preventing Possible Extinction, Genes, 10.3390/genes11050588, 11, 5, (588), (2020).
  • Satellite Tracking Can Inform Population-Level Dispersal to Foraging Grounds of Post-nesting Kemp’s Ridley Sea Turtles, Frontiers in Marine Science, 10.3389/fmars.2020.00559, 7, (2020).
  • Embryonic Temperature Programs Phenotype in Reptiles, Frontiers in Physiology, 10.3389/fphys.2020.00035, 11, (2020).
  • Ecological vulnerability of two sea turtle species in the Gulf of Mexico: an integrated spatial approach, Endangered Species Research, 10.3354/esr00984, 40, (337-356), (2019).
  • The climatic debt of loggerhead sea turtle populations in a warming world, Ecological Indicators, 10.1016/j.ecolind.2019.105657, 107, (105657), (2019).
  • Size‐based differences in isotopic niche width (δ13C and δ15N) of green turtles (Chelonia mydas) nesting on Príncipe Island, Gulf of Guinea, Marine Ecology, 10.1111/maec.12636, 0, 0, (undefined).

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