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Antarctic fur seal stable isotopes

A stable isotope analysis on blood and whiskers samples from adult female Antarctic fur seals, from 3 colonies in the Southern Ocean:

- Marion Island (2008-2018)

- Bird Island, South Georgia (2008-2012)

- Cape Shirreff, South Shetland Islands (2008-2012)


The purpose of the study is to examine temporal, spatial and individual variation in the trophic ecology of Antarctic fur seal, and their role as sentinels of change in the Southern Ocean ecosystem.


EMBARGO NOTE: Data is embargoed until 01/01/2027. The data files associated with this record will be made available at this time.

Simple

Identification info

Date (Publication)
2026-03-17T00:00:00

Identifier

Title
Information and documentation - Digital object identifier system
Citation identifier
ISO 26324:2012

Code
10.25959/64A7-FW78
Codespace
doi.org
Description
Digital Object Identifier (DOI)

Principal investigator

Institute for Marine and Antarctic Studies - Friscourt, Noémie
University of Tasmania
ROR ID >

ORCID >

Principal investigator

Institute for Marine and Antarctic Studies - Lea, Mary-Anne
University of Tasmania
ROR ID >

ORCID >

Collaborator

Institute for Marine and Antarctic Studies - Walters, Andrea
University of Tasmania
ROR ID >

ORCID >

Status
Completed

Principal investigator

Institute for Marine and Antarctic Studies - Lea, Mary-Anne
University of Tasmania
Tasmania
Australia
ROR ID >

ORCID >

Point of contact

Institute for Marine and Antarctic Studies - Walters, Andrea
University of Tasmania
Tasmania
Australia
ROR ID >

ORCID >

Point of contact

Institute for Marine and Antarctic Studies - Friscourt, Noémie
University of Tasmania
Tasmania
Australia
ROR ID >

ORCID >

Topic category
  • Biota

Extent

N
S
E
W


N
S
E
W


N
S
E
W


Temporal extent

Time period
2008-01-01 2012-12-31
Maintenance and update frequency
Irregular
Keywords (Theme)
  • stable isotopes
  • whiskers
  • blood
Keywords (Taxon)
  • Antarctic fur seal
  • Arctocephalus gazella
Global Change Master Directory Earth Science Keywords, Version 8.5
  • ANIMAL SCIENCE
  • ANIMAL ECOLOGY AND BEHAVIOR
  • ANIMAL PHYSIOLOGY AND BIOCHEMISTRY
AODN Geographic Extents Vocabulary
  • Global / Oceans | Global / Oceans | Southern Ocean
Australian and New Zealand Standard Research Classification (ANZSRC): Fields of Research
  • Population Ecology
  • Marine and Estuarine Ecology (incl. Marine Ichthyology)

Resource constraints

Use limitation
Data, products and services from IMAS are provided "as is" without any warranty as to fitness for a particular purpose.

Resource constraints

Other constraints
This dataset is the intellectual property of the University of Tasmania (UTAS) through the Institute for Marine and Antarctic Studies (IMAS).

Resource constraints

Linkage
https://licensebuttons.net/l/by-nc/4.0/88x31.png

License Graphic

Title
Creative Commons Attribution-NonCommercial 4.0 International License
Alternate title
CC-BY-NC
Edition
4.0


>

Website
https://creativecommons.org/licenses/by-nc/4.0/

License Text

Other constraints
Friscourt, N., Lea, M.-A., & Walters, A. (2026). Antarctic fur seal stable isotopes [Data set]. Institute for Marine and Antarctic Studies. https://doi.org/10.25959/64A7-FW78
Language
English
Character encoding
UTF8
Supplemental Information
Friscourt, N., M. A. Lea, Y. Cherel, S. Wotherspoon, E. A. Brewer, W. C. Oosthuizen, P. J. N. de Bruyn, M. Wege, M. E. Goebel, P. N. Trathan, and A. Walters. 2024. Seasonal and ocean basin-scale assessment of amino acid δ15N trends in a Southern Ocean marine predator. Marine Ecology Progress Series 747:151-169. https://doi.org/10.3354/meps14699 Walters, A., M. Hindell, M. E. Goebel, M. N. Bester, P. N. Trathan, W. C. Oosthuizen, and M.-A. Lea. 2020. Southern Ocean isoscapes derived from a wide-ranging circumpolar marine predator, the Antarctic fur seal. Ecological Indicators 118. https://doi.org/10.1016/j.ecolind.2020.106694

Content Information

Content type
Physical measurement

Identifier

Code
Nitrogen stable isotope
Name
Carbon stable isotope

Name
Per mill

Identifier

Code
Carbon stable isotope
Name
Per mille

Distribution Information

Distribution format
  • CSV

OnLine resource
Associated publication

Friscourt, N., M. A. Lea, Y. Cherel, S. Wotherspoon, E. A. Brewer, W. C. Oosthuizen, P. J. N. de Bruyn, M. Wege, M. E. Goebel, P. N. Trathan, and A. Walters. 2024. Seasonal and ocean basin-scale assessment of amino acid δ15N trends in a Southern Ocean marine predator. Marine Ecology Progress Series 747:151-169. https://doi.org/10.3354/meps14699

OnLine resource
Associated publication

Walters, A., M. Hindell, M. E. Goebel, M. N. Bester, P. N. Trathan, W. C. Oosthuizen, and M.-A. Lea. 2020. Southern Ocean isoscapes derived from a wide-ranging circumpolar marine predator, the Antarctic fur seal. Ecological Indicators 118. https://doi.org/10.1016/j.ecolind.2020.106694

Resource lineage

Statement
Samples: whole blood and whiskers of adult female Antarctic fur seals (AFS) Stable isotope analysis: bulk on whiskers and whole blood; compound specific amino acid only on whole blood 1. Sample collection Samples were collected from female AFSs breeding at 3 circumpolar sites in the Southern Ocean: (1) Marion Island (46° 52’ S, 37° 51’ E), in the Indian sector, (2) Bird Island (54° 00’ S, 38° 02’ W), off the northwest tip of South Georgia in the southwest Atlantic sector and (3) Cape Shirreff (62° 28’ S, 60° 48’ W), on the north coast of Livingston Island, in the South Shetland Islands, near the tip of the Antarctic Peninsula on the edge of the Pacific sector. Whole blood samples (1–5 ml) were collected from a hind flipper interdigital vein from adult female AFSs. Blood was sampled as soon as possible after females arrived at the breeding colony and when possible again at the end of the breeding season. Whole blood provides an indication of the consumer trophic ecology over the past 2–3 months. Samples collected at the start of the breeding season thus represent the last few months of the inter-breeding period, while samples collected at the end of the breeding season reflect foraging during the summer breeding period. One of the longest vibrissae, typically most distal to the nose, was cut as close to the face as possible, and the regrowth was cut again when females returned the following summer. 2. Laboratory analysis 2.1. Whole blood bulk and CSIA-AA Samples were stored at –20°C until isotopic analysis. Blood samples were dried at 60°C for at least 24 h prior to bulk and compound-specific stable isotope analyses (Walters et al. 2020 Friscourt et al. 2024). Dried blood samples were analysed for bulk δ13C and δ15N values (δ13Cbulk and δ15Nbulk) by combusting them in a Carlo-Erba EA1100 (CE Instruments) and passing the separated gases produced to an Isoprime (Elementar) continuous-flow isotope ratio mass spectrometer (IRMS). All samples were processed at the Farquhar Laboratory, Australian National University (ANU), Canberra. Replicate measurements of internal laboratory standards for δ15N (glycine, cysteine) and δ13C (glycine, cane sugar and beet sugar) indicated internal precisions better than 0.15‰, for both. Internal standards were previously calibrated against interlaboratory comparison standards distributed by the International Atomic Energy Agency (IAEA) and the USGS (L-glutamic acid, USGS 40 and USGS 41), except for ANU cane sugar, which was also the source of IAEA CH-6. Stable isotope ratios were reported using standard δ notation in parts per thousand (‰) deviation from the international standards Vienna PeeDee belemnite for δ13C and atmospheric nitrogen for δ15N as follows: δX = [(Rsample/Rstandard) – 1] × 1000 (1) where X is 13C or 15N, and R is the corresponding ratio of 13C/12C or 15N/14N. Dried blood samples were analysed for individual amino acid δ15N values (δ15NAA) using a modified method described by Meekan et al. (2022) at the Commonwealth Scientific and Industrial Research Organisation (CSIRO) laboratories in Hobart, Australia (see supplementary material of Friscourt et al. 2024 for more information). The modification was the temperature and duration of the initial hydrolysis; we used 20 h at 110°C. The δ15N compositions of the individual amino acids were measured with a Trace GC Ultra gas chromatograph coupled to a Delta V Plus IRMS through a GC-C combustion furnace (980°C), reduction furnace (650°C) and liquid N2 cold trap. Each sample was analysed at least in duplicate. To normalize the δ15N values, a set of amino acid standards with known δ15N values was used to bracket the 2 distinct IRMS analyses. The slope and intercept of known vs. measured values were then used to correct the measured values for the sample set. The reproducibility of the isotopic analysis of individual amino acids calculated from the bracketing standards was ±0.48‰ (1 SD) and ranged from ±0.10 to ±0.71‰. 2.2 Whiskers bulk Whiskers were cleaned with 3 successive rinses in a 2:1 chloroform:methanol solution, and then oven-dried at 60°C for 72 h. Whiskers were measured, weighed and sectioned into approximately 3 mm sections (0.5-1.5 mg weight) following Walters et al. (2020). Samples were analysed for stable carbon (δ13C) and nitrogen (δ15N) isotopes by combusting them in a Carlo-Erba EA1100 (CE Instruments, Milan, Italy) and passing the separated gases produced to an Isoprime (Elementar, Cheadle SK8 6PT England) continuous-flow isotope-ratio mass spectrometer. All samples were processed at the Farquhar Laboratory, Australian National University (ANU), Canberra. Isotope values were reported using standard δ notation in parts per thousand (‰) deviation from the international standards (Vienna PeeDee Belemnite for carbon, and atmospheric nitrogen for nitrogen) as follows: δX = [(Rsample/Rstandard) – 1] × 1000, where X is 13C or 15N, and R is the corresponding ratio of 13C/12C or 15N/14N. As a control for the quality of keratin, we measured the carbon-to-nitrogen ratios (C:N) of each sample. Most of C:N ratios values are indicating good data quality (Newsome et al. 2010). Samples with a C:N ratio > 3.5 need to be excluded from further analysis. 3. Note on the animal identification. Individual seals are identified using numbered flipper tags. Because seals may be captured and re-tagged multiple times throughout the study period, a single individual can be associated with more than one tag number over time. To account for this, the SIA file includes a seal_tag column indicating the tag number at the time of sample collection, and an other_tag column listing any alternative tag numbers used for the same individual in earlier or later years.
Hierarchy level
Dataset
Hierarchy level
Dataset

Metadata

Metadata identifier
urn:uuid/977fa8d5-da00-4240-8767-e05e532c6bd0

Language
English
Character encoding
UTF8

Distributor

Institute for Marine and Antarctic Studies - (IMAS Data Manager)
IMAS website >

Type of resource

Resource scope
Dataset
Name
IMAS Dataset level record
Metadata linkage
https://metadata.imas.utas.edu.au/geonetwork/srv/eng/catalog.search#/metadata/977fa8d5-da00-4240-8767-e05e532c6bd0

Point of truth URL of this metadata record

Date info (Creation)
2025-09-19T00:00:00
Date info (Revision)
2026-03-17T17:48:22

Metadata standard

Title
ISO 19115-3:2018
 
 

Overviews

Spatial extent

N
S
E
W


N
S
E
W


N
S
E
W


Keywords

blood stable isotopes whiskers
Australian and New Zealand Standard Research Classification (ANZSRC): Fields of Research
Marine and Estuarine Ecology (incl. Marine Ichthyology) Population Ecology
Global Change Master Directory Earth Science Keywords, Version 8.5
ANIMAL ECOLOGY AND BEHAVIOR ANIMAL PHYSIOLOGY AND BIOCHEMISTRY ANIMAL SCIENCE

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