Skip to main content
Log in

Patterns of stable carbon isotope turnover in gag, Mycteroperca microlepis, an economically important marine piscivore determined with a non-lethal surgical biopsy procedure

  • Published:
Environmental Biology of Fishes Aims and scope Submit manuscript

Abstract

To determine the feasibility of using stable isotopes to track diet shifts in wild gag, Mycteroperca microlepis, populations over seasonal timescales, we conducted a repeated measures diet-shift experiment on four adult gag held in the laboratory. Fish were initially fed a diet of Atlantic mackerel, Scomber scombrus, (mean δ13C = −21.3‰ ± 0.2, n = 20) for a period of 56 days and then shifted to a diet of pinfish, Lagodon rhomboids, (mean δ13C = −16.6‰ ± 0.6, n = 20) for the 256 day experiment. We developed a non-lethal surgical procedure to obtain biopsies of the muscle, liver, and gonad tissue monthly from the same four fish. We then determined the δ13C value of each tissue by isotope ratio mass spectrometry. For the gonad tissue we used the relationship between C/N and lipid content to correct for the influence of lipids on δ13C value. We observed a significant shift in the δ13C values of all of the tissues sampled in the study. Carbon turnover rates varied among the three tissues, but the shift in diet from mackerel to pinfish was clearly traceable through analysis of δ13C values. The turnover rates for muscle tissue were 0.005‰ day−1, and for gonad tissue was 0.009‰ day−1. Although it is generally thought that tissue turnover rates in ectotherms are driven primarily by growth, we found that metabolic rate can be a major factor driving tissue turnover in adult gag.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Allendorf F, Brett J, Cowey C, Donaldson E, Fagerlund U, Fange R, Gold J, Grove D, Groves T, Higgs D, Hyatt K, McBride J, Peter R, Ricker W, Terner C (1979) Bioenergetics and growth. Academic, New York, 786 pp

    Google Scholar 

  • Ayliffe LK, Cerling TE, Robinson T, West AG, Sponheimer M, Passey BH, Hammer J, Roeder B, Dearing MD, Ehleringer JR (2004) Turnover of carbon isotopes in tail hair and breath CO2 of horses fed an isotopically varied diet. Oecologia 139:11–22

    Article  PubMed  CAS  Google Scholar 

  • Berkeley S, Chapman C, Sogard S (2004) Maternal age as a determinant of larval growth and survival in a marine fish, Sebastes melanops. Ecology 85:1258–1264

    Article  Google Scholar 

  • Bosley KL, Witting DA, Chambers RC, Wainright SC (2002) Estimating turnover rates of carbon and nitrogen in recently metamorphosed winter flounder Pseudopleuronectes americanus with stable isotopes. Mar Ecol Prog Ser 236:233–240

    Article  Google Scholar 

  • Chanton JP, Lewis FG (2002) Examination of coupling between primary and secondary production in a river-dominated estuary: Apalachicola Bay, Florida, USA. Limnol Oceanogr 47:683–697

    Article  Google Scholar 

  • DeNiro MJ, Epstein S (1977) Mechanism of carbon isotope fractionation associated with lipid synthesis. Science 197:261–263

    Article  PubMed  CAS  Google Scholar 

  • DeNiro MJ, Epstein S (1978) Influence of diet on distribution of carbon isotopes in animals. Geochim Cosmochinica Acta 42:495–506

    Article  CAS  Google Scholar 

  • Folch J, Lees M, Sloane Stanley GH (1957) A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem 497–509

  • Fry B (2006) Stable isotope ecology. Springer, New York, 308 pp

    Book  Google Scholar 

  • Fry B, Parker PL (1979) Animal diet in Texas seagrass meadows—Delta 13 C evidence for the importance of benthic plants. Estuar Coast Mar Sci 8:499–509

    Article  CAS  Google Scholar 

  • Fry B, Arnold C (1982) Rapid C-13/C-12 turnover during growth of brown shrimp (Penaeus aztecus). Oceologia 54:200–204

    Article  Google Scholar 

  • Fry B, Mumford PL, Robblee MB (1999) Stable isotope studies of pink shrimp (Farfantepenaeus duorarum Burkenroad) migrations on the southwestern Florida shelf. Bull Mar Sci 65:419–430

    Google Scholar 

  • Guelinckx J, Maes J, Van Den Driessche P, Geysen B, Dehairs F, Ollevier F (2007) Changes in delta C-13 and delta N-15 in different tissues of juvenile sand goby Pomatoschistus minutus: a laboratory diet-switch experiment. Mar Ecol Prog Ser 341:205–215

    Article  CAS  Google Scholar 

  • Herzka SZ (2005) Assessing connectivity of estuarine fishes based on stable isotope ratio analysis. Estuar Coast Shelf Sci 64:58–69

    Article  Google Scholar 

  • Herzka SZ, Holt GJ (2000) Changes in isotopic composition of red drum (Sciaenops ocellatus) larvae in response to dietary shifts: potential applications to settlement studies. Can J Fish Aquat Sci 57:137–147

    Article  Google Scholar 

  • Herzka SZ, Holt GJ, Holt SA (2001) Documenting the settlement history of individual fish larvae using stable isotope ratios: model development and validation. J Exp Mar Biol Ecol 265:49–74

    Article  Google Scholar 

  • Hesslein RH, Hallard KA, Ramlal P (1993) Replacement of sulfur, carbon, and nitrogen in tissue of growing broad white-fish (Coregonus nasus) in response to a change in diet traced by δ 34 S, δ 13 C, δ 15Ν. Can J Fish Aquat Sci 50:2071–2076

    Article  CAS  Google Scholar 

  • Hobson KA (1999) Tracing origins and migrations of wildlife using stable isotopes: a review. Oceologia 120:314–326

    Article  Google Scholar 

  • Hobson KA, Clark RG (1992) Assessing avian diets using stable isotopes I: turnover of 13 C in tissues. Condor 94:181–188

    Article  Google Scholar 

  • Logan J, Haas HL, Deegan L, Gaines E (2006) Turnover rates of nitrogen stable isotopes in the salt march mummichog, Fundulus heteroclitus, following a laboratory diet switch. Oceologia 147:391–395

    Article  Google Scholar 

  • Logan JM, Lutcavage ME (2008) A comparison of carbon and nitrogen stable isotope ratios of fish tissues following lipid extractions with non-polar and traditional chloroform/methanol solvent systems. Rapid Commun Mass Spectrom 22:1081–1086

    Article  PubMed  CAS  Google Scholar 

  • MacAvoy SE, Macko SA, Garman GC (2001) Isotopic turnover in aquatic predators: quantifying the exploitation of migratory prey. Can J Fish Aquat Sci 58:923–932

    Article  CAS  Google Scholar 

  • McConnaughey T, McRoy CP (1979) Food-web structure and the fractionation of carbon isotopes in the Bering Sea. Mar Biol 53:257–262

    Article  CAS  Google Scholar 

  • Mullaney MD, Gale LD (1996) Ecomorphological relationships in ontogeny and diet in gag, Mycteroperca microlepis (Pisces:Serranidae). Copia 1:167–180

    Article  Google Scholar 

  • Murray MJ (2002) Fish surgery. Semin Avian Exot Pet Med 11:246–257

    Article  Google Scholar 

  • Parker SJ, McElderry HI, Rankin PS, Hannah RW (2006) Buoyancy regulation and barotrauma in two species of nearshore rockfish. Trans Am Fish Soc 135:1213–1223

    Article  Google Scholar 

  • Peterson BJ, Fry B (1987) Stable isotopes in ecosystems studies. Annu Rev Ecol Syst 18:293–320

    Article  Google Scholar 

  • Phillips DL, Eldridge PM (2006) Estimating the timing of diet shifts using stable isotopes. Oceologia 147:195–203

    Article  Google Scholar 

  • Post DM (2002) Using stable isotopes to estimate trophic position: models, methods, and assumptions. Ecology 83:703–718

    Article  Google Scholar 

  • Post DM (2003) Individual variation in the timing of ontogenetic niche shifts in largemouth bass. Ecology 84:1298–1310

    Article  Google Scholar 

  • Post DM, Layman CA, Arrington DA, Takimoto G, Quattrochi J, Montana CG (2007) Getting to the fat of the matter: models, methods, and assumptions for dealing with lipids in stable isotope analyses. Oecologia 152:179–189

    Article  PubMed  Google Scholar 

  • Sheridan MA (1988) Lipid dynamics in fish: aspects of absorption, transportation, deposition, and mobilization. Comp Biochem Physiol 90:679–690

    Article  CAS  Google Scholar 

  • Suring E, Wing SR (2009) Isotopic turnover rate and fractionation in multiple tissues of red rock lobster (Jasus edwardsii) and blue cod (Parapercis colias): consequences for ecological studies. J Exp Mar Biol Ecol 370:56–63

    Article  CAS  Google Scholar 

  • Sweeting CJ, Polunin NVC, Jennings S (2006) Effects of chemical lipid extraction and arithmetic lipid correction on stable isotope ratios of fish tissues. Rapid Commun Mass Spectrom 20:595–601

    Article  PubMed  CAS  Google Scholar 

  • Tieszen LL, Boutton TW, Tesdahl KG, Slade NA (1983) Fractionation and turnover of stable carbon isotopes in animal tissues: implications for delta 13 C analysis of diet. Oceologia 57:32–37

    Article  Google Scholar 

Download references

Acknowledgements

We are grateful to Captain W. Sauls, Panama City, FL, for the use of the F/V Margie Anne for our research; to Captain D. Sauls and crew for assistance onboard in the field; to staff of the Florida State University Coastal and Marine Laboratory (FSUCML), particularly D. Tinsley, B. Henderson, M. Daniels, F. Lindamood, and FSUCML Academic Diving Program for assistance in many aspects of this study; to the Florida State High Magnetic Field Laboratory especially Y. Xu for her assistance with the mass spectrometry, to K. Kingon and N. Hyams (Florida State University) for their assistance in the laboratory; This work was funded through the Northern Gulf Institute, a NOAA Co-operative Institute, NOAA MARFIN NA07NMF4330120 (to Coleman and Koenig), and NOAA Cooperative Research Program NA04NMF4540213 (to Koenig and Coleman).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to James Nelson.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nelson, J., Chanton, J., Coleman, F. et al. Patterns of stable carbon isotope turnover in gag, Mycteroperca microlepis, an economically important marine piscivore determined with a non-lethal surgical biopsy procedure. Environ Biol Fish 90, 243–252 (2011). https://doi.org/10.1007/s10641-010-9736-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10641-010-9736-4

Keywords

Navigation