Register      Login
Australian Journal of Zoology Australian Journal of Zoology Society
Evolutionary, molecular and comparative zoology
RESEARCH ARTICLE

Investigating diet and diet switching in green turtles (Chelonia mydas)

Bonita Prior A , David T. Booth A C and Colin J. Limpus B
+ Author Affiliations
- Author Affiliations

A School of Biological Sciences, The University of Queensland, St Lucia, Qld 4072, Australia.

B Threatened Species Unit, Queensland Government Department of Environment and Heritage Protection, Brisbane, Qld 4001, Australia.

C Corresponding author. Email: d.booth@uq.edu.au

Australian Journal of Zoology 63(6) 365-375 https://doi.org/10.1071/ZO15063
Submitted: 14 October 2015  Accepted: 14 December 2015   Published: 8 January 2016

Abstract

Understanding the dietary ecology of animals provides information about their habitat requirements, facilitating informed conservation. We used last-bite diet and stable isotope analysis to assess the diet of juvenile and adult green turtles (Chelonia mydas) at two different habitats located 10 km apart within Port Curtis, Queensland, Australia. Last-bite diet analysis indicated that turtles had distinctly different diets in these two habitats: in one the diet was dominated by red macroalgae and in the other the diet was dominated by seagrass. Only juveniles (n = 12) were caught in the habitat where red macroalgae dominated the diet, while both juveniles (n = 9) and adults (n = 38) were captured in the habitat where seagrass dominated the diet. In the seagrass habitat there was no difference in diet between juveniles and adults, and no difference in diet between adult males (n = 17) and females (n = 21).

Because the red macroalgae and seagrass had distinctly different carbon stable isotope ratios, it was possible to detect a change in diet by comparing the carbon stable isotope ratio between serum and epidermal tissue sampled from the same turtle. In this region, a switch in diet would reflect a shift in foraging habitat. Such comparisons indicate that ~50% of turtles switched diet, and therefore changed foraging habitat between the time when blood serum and epidermis were formed. This implies that switching foraging habitat by green turtles within this region is a common occurrence, which is somewhat surprising because previously it was thought that foraging green turtles had high site fidelity with relatively small home ranges.

Additional keywords: foraging, sea turtle, SIA, stable isotopes.


References

Arthur, K. E., O’Neil, J. M., Limpus, C. J., Abernathy, K., and Marshall, G. (2007). Using animal-borne imaging to assess green turtle (Chelonia mydas) foraging ecology in Moreton Bay, Australia. Marine Technology Society Journal 41, 9–13.
Using animal-borne imaging to assess green turtle (Chelonia mydas) foraging ecology in Moreton Bay, Australia.Crossref | GoogleScholarGoogle Scholar |

Arthur, K. E., Boyle, M. C., and Limpus, C. J. (2008). Ontogenetic changes in diet and habitat use in green sea turtle (Chelonia mydas) life history. Marine Ecology Progress Series 362, 303–311.
Ontogenetic changes in diet and habitat use in green sea turtle (Chelonia mydas) life history.Crossref | GoogleScholarGoogle Scholar |

Arthur, K. E., McMahon, K. M., Limpus, C. J., and Dension, W. C. (2009). Feeding ecology of green turtles (Chelonia mydas) from Shoalwater Bay, Australia. Marine Turtle Newsletter 123, 6–12.

Babcock, R. C., Baird, M. E., Pillans, R., Patterson, T., Clementson, L. A., Haywood, M. E., Rochester, W., Morello, E., Keely, N., Oubelkheir, K., Fry, G., Dubadain, M., Perkins, S., Forcey, K., Cooper, S., Donovan, A., Kenyon, R., Carlin, G., and Limpus, C. (2015). Towards an integrated study of the Gladstone marine system. CSIRO Oceans and Atmosphere Flagship, Brisbane.

Bjorndal, K. A. (1980). Nutrition and grazing behavior of the green turtle Chelonia mydas. Marine Biology 56, 147–154.
Nutrition and grazing behavior of the green turtle Chelonia mydas.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXlsVyktrw%3D&md5=b360744b03e790236cc827c784318fd4CAS |

Bjorndal, K. A. (1997). Foraging ecology and nutrition of sea turtles. In ‘The Biology of Sea Turtles’. (Eds P. L. Lutz and J. A. Musick.) pp. 199–232. (CRC Press: Boca Raton, FL.)

Bjorndal, K. A., Bolten, A. B., Langeux, C. J., and Jackson, D. R. (1997). Dietary overlap in three sympatric congeneric freshwater turtles (Pseudmys) in Florida. Chelonian Conservation and Biology 2, 430–433.

Bowen, B. W., Meylan, A. B., Ross, J. P., Limpus, C. J., Balazs, G. H., and Avise, J. C. (1992). Global population structure and natural history of the green turtle (Chelonia mydas) in terms of matriarchal phylogeny. Evolution 46, 865–881.
Global population structure and natural history of the green turtle (Chelonia mydas) in terms of matriarchal phylogeny.Crossref | GoogleScholarGoogle Scholar |

Brine, M. (2008). Feeding habits of green turtles in two Australian foraging grounds: insights from stable isotope analysis and oesophageal lavage. B.Sc.(Honours) Thesis, University of Queensland, Brisbane.

Broderick, A. C., Coyne, M. S., Fuller, W. J., Glen, F., and Godley, B. J. (2007). Fidelity and over-wintering of sea turtles. Proceedings of the Royal Society B: Biological Sciences 274, 1533–1539.
Fidelity and over-wintering of sea turtles.Crossref | GoogleScholarGoogle Scholar | 17456456PubMed |

Burkholder, D. A., Heithaus, M. R., Thomson, J. A., and Fourqurean, J. W. (2011). Diversity in trophic interactions of green sea turtles Chelonia mydas on a relatively pristine coastal foraging ground. Marine Ecology Progress Series 439, 277–293.
Diversity in trophic interactions of green sea turtles Chelonia mydas on a relatively pristine coastal foraging ground.Crossref | GoogleScholarGoogle Scholar |

Cameron, A. M. D. (2007). Diet composition of juvenile green turtles (Chelonia mydas) from an unusual stranding aggregation in Hervey Bay: insights into diet using microscopy and stable isotope analysis. B.Sc.(Honours) Thesis, University of Queensland, Brisbane.

Carman, V. G., Botto, F., Gaitán, E., Albareda, D., Campagna, C., and Mianzan, H. (2014). A jellyfish diet for the herbivorous green turtle Chelonia mydas in the temperate SW Atlantic. Marine Biology 161, 339–349.
A jellyfish diet for the herbivorous green turtle Chelonia mydas in the temperate SW Atlantic.Crossref | GoogleScholarGoogle Scholar |

Carpentier, A. S., Booth, D. T., Arthur, K. E., and Limpus, C. J. (2015). Stable isotope relationships between mothers, eggs and hatchlings in loggerhead sea turtles Caretta caretta. Marine Biology 162, 783–797.
Stable isotope relationships between mothers, eggs and hatchlings in loggerhead sea turtles Caretta caretta.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2MXisVOrurs%3D&md5=a59108ee42607db1aaed88447627d7ecCAS |

Ceriani, S. A., Roth, J. D., Tucker, A. D., Evans, D. R., Addison, D. S., Sasso, C. R., Ehrhart, L. M., and Weishampel, J. F. (2015). Carry-over effects and foraging ground dynamics of a major loggerhead breeding aggregation. Marine Biology 162, 1955–1968.
Carry-over effects and foraging ground dynamics of a major loggerhead breeding aggregation.Crossref | GoogleScholarGoogle Scholar |

Chaloupka, M., Limpus, C., and Miller, J. (2004). Green turtle somatic growth dynamics in a spatially disjunct Great Barrier Reef metapopulation. Coral Reefs 23, 325–335.
Green turtle somatic growth dynamics in a spatially disjunct Great Barrier Reef metapopulation.Crossref | GoogleScholarGoogle Scholar |

Connolly, R. M. (2003). Differences in trophodynamics of commercially important fish between artificial waterways and natural coastal wetlands. Estuarine, Coastal and Shelf Science 58, 929–936.
Differences in trophodynamics of commercially important fish between artificial waterways and natural coastal wetlands.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXpt1yqs7k%3D&md5=3d57cf895845332fd034c296f6fc15caCAS |

Cribb, A. B. (1996). ‘Seaweeds of Queensland: a Naturalist’s Guide.’ (The Queensland Naturalist’s Club: Brisbane.)

Deniro, M. J., and Epstein, S. (1981). Influence of diet on the distribution of nitrogen isotopes in animals. Geochimica et Cosmochimica Acta 45, 341–351.
Influence of diet on the distribution of nitrogen isotopes in animals.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3MXktVGmtLw%3D&md5=137328286c7936d82ec8ecf0c9a310ccCAS |

Duke, N. (2006). ‘The Authoritative Guide to Australia’s Mangrove Plants.’ (The University of Queensland Centre for Marine Studies: Brisbane.)

Forbes, G., and Limpus, C. (1993). A non-lethal method for retrieving stomach contents from sea turtles. Wildlife Research 20, 339–343.
A non-lethal method for retrieving stomach contents from sea turtles.Crossref | GoogleScholarGoogle Scholar |

Garnett, S., Price, I., and Scott, F. (1985). The diet of the green turtle, Chelonia Mydas (L.), in Torres Strait. Wildlife Research 12, 103–112.
The diet of the green turtle, Chelonia Mydas (L.), in Torres Strait.Crossref | GoogleScholarGoogle Scholar |

Hazel, J., Hamann, M., and Lawler, I. R. (2013). Home range of immature green turtles tracked at an offshore tropical reef using automated passive acoustic technology. Marine Biology 160, 617–627.
Home range of immature green turtles tracked at an offshore tropical reef using automated passive acoustic technology.Crossref | GoogleScholarGoogle Scholar |

Heithaus, M. R., McLash, J. J., Frid, A., Dill, L. M., and Marshall, G. J. (2002). Novel insights into green sea turtle behaviour using animal-borne video cameras. Journal of the Marine Biological Association of the United Kingdom 82, 1049–1050.
Novel insights into green sea turtle behaviour using animal-borne video cameras.Crossref | GoogleScholarGoogle Scholar |

Hobson, K. A., and Clark, R. G. (1992). Assessing avian diets using stable isotopes. I: turnover of 13C in tissues. The Condor 94, 181–188.
Assessing avian diets using stable isotopes. I: turnover of 13C in tissues.Crossref | GoogleScholarGoogle Scholar |

Hobson, K. A., and Clark, R. G. (1993). Turnover of 13C in cellular and plasma fractions of blood: implications for nondestructive sampling in avian dietary studies. The Auk 110, 638–641.
Turnover of 13C in cellular and plasma fractions of blood: implications for nondestructive sampling in avian dietary studies.Crossref | GoogleScholarGoogle Scholar |

Lanyon, J. M. (1986).’Guide to the Identification of Seagrasses in the Great Barrier Reef Region.’ (Nadicprint Services: Townsville.)

Lemons, G., Lewison, R., Komoroske, L., Gaos, A., Lai, C.-T., Dutton, P., Eguchi, T., LeRoux, R., and Seminoff, J. A. (2011). Trophic ecology of green sea turtles in a highly urbanized bay: insights from stable isotopes and mixing models. Journal of Experimental Marine Biology and Ecology 405, 25–32.
Trophic ecology of green sea turtles in a highly urbanized bay: insights from stable isotopes and mixing models.Crossref | GoogleScholarGoogle Scholar |

Lemons, G. E., Eguchi, T., Lyon, B. N., LeRoux, R., and Seminoff, J. A. (2012). Effects of blood anticoagulants on stable isotope values of sea turtle blood tissue. Aquatic Biology 14, 201–206.
Effects of blood anticoagulants on stable isotope values of sea turtle blood tissue.Crossref | GoogleScholarGoogle Scholar |

Limpus, C., and Chaloupka, M. (1997). Nonparametric regression modelling of green sea turtle growth rates (southern Great Barrier Reef). Marine Ecology Progress Series 149, 23–34.
Nonparametric regression modelling of green sea turtle growth rates (southern Great Barrier Reef).Crossref | GoogleScholarGoogle Scholar |

Limpus, C. J., and Reed, P. C. (1985). The green sea turtle, Chelonia mydas, in Queensland: a preliminary description of the population structure of a coral reef feeding ground. In ‘Biology of Austrlaian Frogs and Reptiles’. (Eds G. C. Grigg, R. Shine and H. Ehmann.) pp. 47–52. (Royal Zoological Society of New South Wales: Sydney.)

Makowski, C., Seminoff, J. A., and Salmon, M. (2006). Home range and habitat use of juvenile Atlantic green turtles (Chelonia mydas L.) on shallow reef habitats in Palm Beach, Florida, USA. Marine Biology 148, 1167–1179.
Home range and habitat use of juvenile Atlantic green turtles (Chelonia mydas L.) on shallow reef habitats in Palm Beach, Florida, USA.Crossref | GoogleScholarGoogle Scholar |

McCormack, C., Rasheed, M. A., Davies, J., Carter, A., Sankey, T., and Tol, S. (2013). Long term seagrass monitoring in the Port Curtis Western Basin. In ‘Quarterly Seagrass Assessments & Permanent Transect Monitoring Progress Report Nov 2009 to Nov 2012’. (Ed. TropWATER.) pp. 1–232. (James Cook University: Townsville.)

Peterson, B. J., and Fry, B. (1987). Stable isotopes in ecosystem studies. Annual Review of Ecology and Systematics 18, 293–320.
Stable isotopes in ecosystem studies.Crossref | GoogleScholarGoogle Scholar |

Post, D. M., Layman, C. A., Arrington, D. A., Takimoto, G., and Quattrochi, J. (2007). Getting to the fat of the matter: models, methods and assumptions for dealing with lipids in stable isotope analyses. Oecologia 152, 179–189.
Getting to the fat of the matter: models, methods and assumptions for dealing with lipids in stable isotope analyses.Crossref | GoogleScholarGoogle Scholar | 17225157PubMed |

Raven, J. A., Johnston, A. M., Kubler, J. E., Korb, R., McInroy, S. G., Handley, L. L., Scrimgeour, C. M., Walker, D. I., Beardall, J., Vanderklift, M., Fredriksen, S., and Dunton, K. H. (2002). Mechanistic interpretation of carbon isotope discrimination by marine macroalgae and seagrasses. Functional Plant Biology 29, 355–378.
Mechanistic interpretation of carbon isotope discrimination by marine macroalgae and seagrasses.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XjsVCltLw%3D&md5=87b377e24d7bf2e3140da3fab36c5865CAS |

Reich, K. J., Bjorndal, K. A., and Martinez del Rio, C. (2008). Effects of growth and tissue type on the kinetics of 13C and 15N incorporation in a rapidly growing ectotherm. Oecologia 155, 651–663.
Effects of growth and tissue type on the kinetics of 13C and 15N incorporation in a rapidly growing ectotherm.Crossref | GoogleScholarGoogle Scholar | 18188602PubMed |

Reisser, J., Proietti, M., Sazima, I., Kinas, P., Horta, P., and Secchi, E. (2013). Feeding ecology of the green turtle (Chelonia mydas) at rocky reefs in western South Atlantic. Marine Biology 160, 3169–3179.
Feeding ecology of the green turtle (Chelonia mydas) at rocky reefs in western South Atlantic.Crossref | GoogleScholarGoogle Scholar |

Schofield, G., Hobson, V. J., Fossette, S., Lilley, M. K. S., Katselidis, K. A., and Hays, G. C. (2010). Fidelity to foraging sites, consistency of migration routes and habitat modulation of home range on sea turtles. Diversity & Distributions 16, 840–853.
Fidelity to foraging sites, consistency of migration routes and habitat modulation of home range on sea turtles.Crossref | GoogleScholarGoogle Scholar |

Seminoff, J. A., Resendiz, A., and Nichols, W. J. (2002). Home range of green turtles Chelonia mydas at a coastal foraging area in the Gulf of California, Mexico. Marine Ecology Progress Series 242, 253–265.
Home range of green turtles Chelonia mydas at a coastal foraging area in the Gulf of California, Mexico.Crossref | GoogleScholarGoogle Scholar |

Seminoff, J. A., Jones, T. T., Eguchi, T., Jones, D. R., and Dutton, P. H. (2006). Stable isotope discrimination (Δ13C and Δ15N) between soft tissues of the green sea turtle Chelonia mydas and its diet. Marine Ecology Progress Series 308, 271–278.
Stable isotope discrimination (Δ13C and Δ15N) between soft tissues of the green sea turtle Chelonia mydas and its diet.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xks1Cjtro%3D&md5=7aaeb60440333926b002d36e11c8534fCAS |

Seminoff, J. A., Za’rate, P., Coyne, M., Foley, D., Parker, D., Lyon, B. N., and Dutton, P. H. (2008). Post-nesting migrations of Galapagos green turtles, Chelonia mydas, in relation to oceanographic conditions: integrating satellite telemetry with remotely-sensed ocean data. Endangered Species Research 4, 57–72.
Post-nesting migrations of Galapagos green turtles, Chelonia mydas, in relation to oceanographic conditions: integrating satellite telemetry with remotely-sensed ocean data.Crossref | GoogleScholarGoogle Scholar |

Tieszen, L. L., Boutton, T. W., Tesdahl, K. G., and Slade, N. A. (1983). Fractionation and turnover of stable carbon isotopes in animal tissues: implications for δ13C analysis of diet. Oecologia 57, 32–37.
Fractionation and turnover of stable carbon isotopes in animal tissues: implications for δ13C analysis of diet.Crossref | GoogleScholarGoogle Scholar |

Vander Zanden, H. B., Bjorndal, K. A., Mustin, W., Ponciano, J. M., and Bolten, A. B. (2012). Inherent variation in stable isotope values and discrimination factors in two life stages of green turtles. Physiological and Biochemical Zoology 85, 431–441.
Inherent variation in stable isotope values and discrimination factors in two life stages of green turtles.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhsVCrt7zF&md5=9390f12a8672cff911391822e3184eb1CAS | 22902371PubMed |

Vander Zanden, H., Pfaller, J., Reich, K., Pajuelo, M., Bolten, A., Williams, K., Frick, M., Shamblin, B., Nairn, C., and Bjorndal, K. (2014a). Foraging areas differentially affect reproductive output and interpretation of trends in abundance of loggerhead turtles. Marine Biology 161, 585–598.
Foraging areas differentially affect reproductive output and interpretation of trends in abundance of loggerhead turtles.Crossref | GoogleScholarGoogle Scholar |

Vander Zanden, H. B., Tucker, A. D., Bolten, A. B., Reich, K. J., and Bjorndal, K. A. (2014b). Stable isotopic comparison between loggerhead sea turtle tissues. Rapid Communications in Mass Spectrometry 28, 2059–2064.
Stable isotopic comparison between loggerhead sea turtle tissues.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXhsVWqsr%2FK&md5=9a222376962284809b631fade1d41d4fCAS | 25156595PubMed |

Vander Zanden, M. J., Clayton, M. K., Moody, E. K., and Solomon, C. T. (2015). Stable isotope turnover and half-life in animal tissues: a literature synthesis. PLoS One 10, e0116182.
Stable isotope turnover and half-life in animal tissues: a literature synthesis.Crossref | GoogleScholarGoogle Scholar | 25635686PubMed |

Winemiller, K. O., Akin, S., and Zeug, S. C. (2007). Production sources and food web structure of a temperate tidal estuary: integration of dietary and stable isotope data. Marine Ecology Progress Series 343, 63–76.
Production sources and food web structure of a temperate tidal estuary: integration of dietary and stable isotope data.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVyrs7%2FL&md5=debb1cf65b03aa387cda484bb26389daCAS |