Skip to main content
Log in

Turnover of carbon isotopes in tail hair and breath CO2 of horses fed an isotopically varied diet

  • Ecophysiology
  • Published:
Oecologia Aims and scope Submit manuscript

Abstract

Temporal stable isotope records derived from animal tissues are increasingly studied to determine dietary and climatic histories. Despite this, the turnover times governing rates of isotope equilibration in specific tissues following a dietary isotope change are poorly known. The dietary isotope changes recorded in the hair and blood bicarbonate of two adult horses in this study are found to be successfully described by a model having three exponential isotope pools. For horse tail hair, the carbon isotope response observed following a dietary change from a C3 to a C4 grass was consistent with a pool having a very fast turnover rate (t 1/2~0.5 days) that made up ~41% of the isotope signal, a pool with an intermediate turnover rate (t 1/2 ~4 days) that comprised ~15% of the isotope signal, and a pool with very slow turnover rate (t 1/2 ~140 days) that made up ~44% of the total isotope signal. The carbon isotope signature of horse blood bicarbonate, in contrast, had a different isotopic composition, with ~67% of the isotope signal coming from a fast turnover pool (t 1/2 0.2 days), ~17% from a pool with an intermediate turnover rate (t 1/2 ~3 days) and ~16% from a pool with a slow turnover rate (t 1/2 ~50 days). The constituent isotope pools probably correspond to one exogenous and two endogenous sources. The exogenous source equates to our fast turnover pool, and the pools with intermediate and slow turnover rates are thought to derive from the turnover of metabolically active tissues and relatively inactive tissues within the body, respectively. It seems that a greater proportion of the amino acids available for hair synthesis come from endogenous sources compared to the compounds undergoing cellular catabolism in the body. Consequently, the isotope composition of blood bicarbonate appears to be much more responsive to dietary isotope changes, whereas the amino acids in the blood exhibit considerable isotopic inertia.

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.

Institutional subscriptions

Fig. 1a, b
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8a, b
Fig. 9a, b

Similar content being viewed by others

References

  • Ambrose SH, Norr L (1993) Carbon isotopic evidence for routing of dietary protein to bone collagen, and whole diet to bone apatite carbonate: purified diet growth experiments. In: Lambert J, Grupe G (eds) Molecular archaeology of prehistoric human bone. Springer, Berlin Heidelberg New York, pp 1–37

  • Bender DA (1985) Amino acid metabolism. Wiley, New York

  • Cerling TE, Harris JM (1999) Carbon isotope fractionation between diet and bioapatite in ungulate mammals and implications for ecological and palaeoecological studies. Oecologia 120:347–363

    Article  Google Scholar 

  • Cerling TE, Harris JM, Passey BH (2003) Dietary preferences of East African bovidea based on stable isotope analysis. J Mammal 84:456–470

    Google Scholar 

  • Cerling TE, Passey BH, Cook CS, Ehleringer JR, Harris JM, Kasiki SM, Dhidha MB (2004) An orphan’s tale: seasonal dietary changes in elephants from Tsavo National Park, Kenya. Palaeogeog Palaeoclimatol Palaeoecol (in press)

  • Craig H (1954) Carbon-13 in plants and the relationships between carbon-13 and carbon-14 variations in nature. J Geol 62:115–149

    CAS  Google Scholar 

  • Criss RE (1999) Principles of stable isotope distribution. Oxford University Press, Oxford

  • Criss RE, Gregory RT, Taylor HP (1987) Kinetic theory of oxygen isotope exchange between minerals and water. Geochim Cosmochim Acta 51:1099–1108

    Article  CAS  Google Scholar 

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

    CAS  PubMed  Google Scholar 

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

    CAS  Google Scholar 

  • Faure G (1977) Principles of isotope geology. Wiley, New York

  • Fricke HC, Clyde WC, O’Neil JR (1998) Intra-tooth variations in δ18O(PO4) of mammalian tooth enamel as a record of seasonal variations in continental climate variables. Palaeogeogr Palaeoclimatol Palaeoecol 126:91–99

    Article  Google Scholar 

  • Friedlander G, Kennedy JW, Macias ES, Miller JM (1981) Nuclear and radiochemistry. Wiley, New York

  • Gadbury C, Tood L, Jaren AH, Amundson R (2000) Spatial and temporary variations in the isotopic composition of bison tooth enamel from the early Holocene Hudson-Meng bone bed. Palaeogeogr Palaeoclimatol Palaeoecol 157:79–93

    Article  Google Scholar 

  • Hilderbrand GV, Farley SD, Robbins CT, Hanley TA, Titus K, Servheen C (1996) Use of stable isotopes to determine diets of living and extinct bears. Can J Zool 74:2080–2088

    Google Scholar 

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

    Google Scholar 

  • Hobson KA, Clarke RG (1993) Turnover of 13C in cellular and plasma fractions of blood: implications for nondestructive sampling in avian dietary studies. Auk 110:638–641

    Google Scholar 

  • Jones RJ, Ludlow MM, Troughton JH, Blunt CG (1981) Changes in the natural carbon isotope ratios of the hair from steers fed diets of C4, C3 and C4 species in sequence. Search 12:85–87

    CAS  Google Scholar 

  • Lee-Thorp J, van der Merwe NJ (1987) Carbon isotope analysis of fossil bone apatite. S Afr J Sci 83:712–715

    Google Scholar 

  • LeGeros RZ (1981) Apatites in biological systems. In: Pamplin B (ed) Inorganic biological crystal growth, progress in crystal growth, and characterization, vol 4. Pergamon, New York, pp 1–45

  • MacFadden BJ (2000) Middle Pleistocene climate change recorded in fossil mammal teeth from Tarijia, Bolivia, and upper limit of the Ensenadan Land-Mammal Age. Quat Res 54:121–131

    Article  CAS  Google Scholar 

  • O’Connell TC, Hedges REM (1999) Investigation into the effect of diet on modern human hair isotopic values. Am J Phys Anthropol 108:409–425

    Article  CAS  PubMed  Google Scholar 

  • Overman RT, Clark HM (1960) Radioisotope techniques. McGraw-Hill, New York

  • Passey BH, Cerling TE (2002) Tooth enamel mineralization in ungulates: implications for recovering a primary isotopic time-series. Geochim Cosmochim Acta 66:3225–3234

    Article  CAS  Google Scholar 

  • Ryder ML (1958) Nutritional factors influencing hair and wool growth. In: Montagna W, Ellis RA (eds) The biology of hair growth. Academic Press, New York, pp 305–334, 520

  • Sharp ZD, Cerling TE (1998) Fossil isotope records of seasonal climate and ecology: straight from the horse’s mouth. Geology 26:219–222

    Article  CAS  Google Scholar 

  • Simon O (1989) Metabolism of proteins and amino acids. In: Bock HD, Eggum BO, Low AG, Simon O, Zebrowska T (eds) Protein metabolism in farm animals. Evaluation, digestion, adsorption, and metabolism. Oxford University Press, Oxford, pp 273–363

  • Tieszen LL, Fagre T (1993) Effect of diet quality and composition on the isotope composition of respiratory CO2, bone collagen, bioapatite, and soft tissues. In: Lambert J, Grupe G (eds) Molecular archaeology of prehistoric human bone. Springer, Berlin Heidelberg New York

  • Tieszen LL, Boutton TW, Tesdahl KG, Slade NA (1983) Fractionation and turnover of stable carbon isotopes in animal tissue: implications for δ13C analysis of diet. Oecologia 57:32–37

    Google Scholar 

  • Waterlow JC, Garlick PJ, Millward DJ (1978) Protein turnover in mammalian tissues and in the whole body. Elsevier/North-Holland Biomedical Press, Amsterdam

  • White CD, Schwarcz HP (1994) Temporal trends in stable isotopes for nubian mummy tissues. Am J Phys Anthropol 93:165–187

    CAS  PubMed  Google Scholar 

  • Wiedemann FB, Bocherens H, Mariotti A, von den Driesch A, Grupe G (1999) Methodological and archaeological implications of intra-tooth variations (δ13C, δ18O) in herbivores from Ain Ghazal (Jordan, Neolithic). J Archaeol Sci 26:697–704

    Article  Google Scholar 

  • Witt GB, Moll EJ, Beeton RJS, Murray PJ (1998) Isotopes, wool, and rangeland monitoring: let the sheep do the sampling. Environ Manage 22:145–152

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

Funding to support this research was provided by the Packard Foundation, Brigham Young University (BYU), and The University of Utah. The authors are much indebted to the students and staff of the BYU animal facility and Y. Rahman for help with sample collection and animal care. C. Cook and M. Lott are thanked for providing technical support in the SIRFER mass spectrometer lab.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to T. E. Cerling.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ayliffe, L.K., Cerling, T.E., Robinson, T. et al. Turnover of carbon isotopes in tail hair and breath CO2 of horses fed an isotopically varied diet. Oecologia 139, 11–22 (2004). https://doi.org/10.1007/s00442-003-1479-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00442-003-1479-x

Keywords

Navigation