Teleost and elasmobranch eye lenses as a target for life-history stable isotope analyses

Incrementally grown, metabolically inert tissues such as fish otoliths provide biochemical records that can used to infer behavior and physiology throughout the lifetime of the individual. Organic tissues are particularly useful as the stable isotope composition of the organic component can provide...

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Main Authors: Katie Quaeck-Davies, Victoria A. Bendall, Kirsteen M. MacKenzie, Stuart Hetherington, Jason Newton, Clive N. Trueman
Format: Article
Language:English
Published: PeerJ Inc. 2018-06-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/4883.pdf
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author Katie Quaeck-Davies
Victoria A. Bendall
Kirsteen M. MacKenzie
Stuart Hetherington
Jason Newton
Clive N. Trueman
author_facet Katie Quaeck-Davies
Victoria A. Bendall
Kirsteen M. MacKenzie
Stuart Hetherington
Jason Newton
Clive N. Trueman
author_sort Katie Quaeck-Davies
collection DOAJ
description Incrementally grown, metabolically inert tissues such as fish otoliths provide biochemical records that can used to infer behavior and physiology throughout the lifetime of the individual. Organic tissues are particularly useful as the stable isotope composition of the organic component can provide information about diet, trophic level and location. Unfortunately, inert, incrementally grown organic tissues are relatively uncommon. The vertebrate eye lens, however, is formed via sequential deposition of protein-filled fiber cells, which are subsequently metabolically inert. Lenses therefore have the potential to serve as biochemical data recorders capturing life-long variations in dietary and spatial ecology. Here we review the state of knowledge regarding the structure and formation of fish eye lenses in the context of using lens tissue for retrospective isotopic analysis. We discuss the relationship between eye lens diameter and body size, describe the successful recovery of expected isotopic gradients throughout ontogeny and between species, and quantify the isotopic offset between lens protein and white muscle tissue. We show that fish eye lens protein is an attractive host for recovery of stable isotope life histories, particularly for juvenile life stages, and especially in elasmobranchs lacking otoliths, but interpretation of lens-based records is complicated by species-specific uncertainties associated with lens growth rates.
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spelling doaj.art-2e2c49f483574c6193ab1d8d8cba1ab22023-12-03T10:52:04ZengPeerJ Inc.PeerJ2167-83592018-06-016e488310.7717/peerj.4883Teleost and elasmobranch eye lenses as a target for life-history stable isotope analysesKatie Quaeck-Davies0Victoria A. Bendall1Kirsteen M. MacKenzie2Stuart Hetherington3Jason Newton4Clive N. Trueman5Ocean and Earth Science, University of Southampton, Southampton, United KingdomCentre for Environment, Fisheries and Aquaculture Science, Lowestoft, United KingdomInstitute of Marine Research/Havforskningsinstituttet, Bergen, NorwayCentre for Environment, Fisheries and Aquaculture Science, Lowestoft, United KingdomScottish Universities Environmental Research Centre, University of Glasgow, Glasgow, United KingdomOcean and Earth Science, University of Southampton, Southampton, United KingdomIncrementally grown, metabolically inert tissues such as fish otoliths provide biochemical records that can used to infer behavior and physiology throughout the lifetime of the individual. Organic tissues are particularly useful as the stable isotope composition of the organic component can provide information about diet, trophic level and location. Unfortunately, inert, incrementally grown organic tissues are relatively uncommon. The vertebrate eye lens, however, is formed via sequential deposition of protein-filled fiber cells, which are subsequently metabolically inert. Lenses therefore have the potential to serve as biochemical data recorders capturing life-long variations in dietary and spatial ecology. Here we review the state of knowledge regarding the structure and formation of fish eye lenses in the context of using lens tissue for retrospective isotopic analysis. We discuss the relationship between eye lens diameter and body size, describe the successful recovery of expected isotopic gradients throughout ontogeny and between species, and quantify the isotopic offset between lens protein and white muscle tissue. We show that fish eye lens protein is an attractive host for recovery of stable isotope life histories, particularly for juvenile life stages, and especially in elasmobranchs lacking otoliths, but interpretation of lens-based records is complicated by species-specific uncertainties associated with lens growth rates.https://peerj.com/articles/4883.pdfSharkTeleostCarbonNitrogenSclerochronology
spellingShingle Katie Quaeck-Davies
Victoria A. Bendall
Kirsteen M. MacKenzie
Stuart Hetherington
Jason Newton
Clive N. Trueman
Teleost and elasmobranch eye lenses as a target for life-history stable isotope analyses
PeerJ
Shark
Teleost
Carbon
Nitrogen
Sclerochronology
title Teleost and elasmobranch eye lenses as a target for life-history stable isotope analyses
title_full Teleost and elasmobranch eye lenses as a target for life-history stable isotope analyses
title_fullStr Teleost and elasmobranch eye lenses as a target for life-history stable isotope analyses
title_full_unstemmed Teleost and elasmobranch eye lenses as a target for life-history stable isotope analyses
title_short Teleost and elasmobranch eye lenses as a target for life-history stable isotope analyses
title_sort teleost and elasmobranch eye lenses as a target for life history stable isotope analyses
topic Shark
Teleost
Carbon
Nitrogen
Sclerochronology
url https://peerj.com/articles/4883.pdf
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