Tissue and fixative dependent shifts of δ 13 C and δ 15 N in preserved ecological material

Abstract Carbon and nitrogen stable isotope analyses are routinely used to investigate aquatic food webs, and have potential application in retrospective investigations using archived materials. However, such analyses assume that storage does not alter isotopic signatures of materials preserved, or...

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Bibliographic Details
Published in:Rapid Communications in Mass Spectrometry
Main Authors: Sweeting, C. J., Polunin, N. V. C., Jennings, S.
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2004
Subjects:
Online Access:http://dx.doi.org/10.1002/rcm.1661
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Frcm.1661
https://onlinelibrary.wiley.com/doi/full/10.1002/rcm.1661
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Summary:Abstract Carbon and nitrogen stable isotope analyses are routinely used to investigate aquatic food webs, and have potential application in retrospective investigations using archived materials. However, such analyses assume that storage does not alter isotopic signatures of materials preserved, or that changes in isotopic composition during storage are predictable. Here we examine preservation shifts on cod ( Gadus morhua ) muscle, roe and liver tissue over 21 months following preservation in 80% ethanol, in 4% formaldehyde, and by freezing. Preservation shifts were not consistent among tissues. High protein tissues exhibited greater δ 15 N shifts than low protein tissues in 4% formaldehyde, while greater δ 13 C shifts occurred in relatively higher fat tissues when preserved in alcohol. Freezing did not change isotopic signatures. Responses of δ 15 N and δ 13 C are explained by differences in the preservative's isotopic signature and the reaction properties and biochemical composition of the tissues preserved. The results clarify some of the processes that lead to isotopic change during preservation. Copyright © 2004 John Wiley & Sons, Ltd.