Diet–tissue discrimination factors ( δ 15 N and δ 13 C values) for blood components in Magellanic ( Spheniscus magellanicus ) and southern rockhopper ( Eudyptes chrysocome ) penguins

2020 ◽  
Vol 34 (6) ◽  
Author(s):  
Edward Jenkins ◽  
Julia Gulka ◽  
David J. Yurkowski ◽  
Gail K. Davoren ◽  
Lana Gonzalez
2011 ◽  
Vol 89 (4) ◽  
pp. 343-347 ◽  
Author(s):  
J.-F. Therrien ◽  
G. Fitzgerald ◽  
G. Gauthier ◽  
J. Bêty

Analysis of carbon (13C/12C) and nitrogen (15N/14N) stable isotope ratios (hereafter δ13C and δ15N, respectively) in animal tissues is a powerful tool in food-web studies. However, isotopic ratios of prey are not transmitted directly to a consumer, as a diet–tissue discrimination factor (denoted Δ) occurs between sources and consumer’s tissues. An accurate assessment of the diet of a consumer with stable isotopes thus requires that the Δ13C and Δ15N of the studied species are known. Our aim was to establish Δ13C and Δ15N values in the Snowy Owl ( Bubo scandiacus (L., 1758)). Moreover, we assessed the potential effect of ethanol preservation of blood samples on δ13C and δ15N values. We kept four captive adult Snowy Owls on a pure diet of mice for ≥6 weeks. We then collected mouse muscle and blood samples from the owls and analyzed their δ13C and δ15N values. Δ13C and Δ15N values (mean ± SE) for owl blood were +0.3‰ ± 0.2‰ and +1.9‰ ± 0.1‰, respectively. These values are the first discrimination factors ever reported in Strigiformes and are lower, for Δ15N, than those obtained in terrestrial carnivores and other bird species, including falcons. Preservation in ethanol did not significantly affect δ13C and δ15N values.


PLoS ONE ◽  
2013 ◽  
Vol 8 (10) ◽  
pp. e77567 ◽  
Author(s):  
Jill A. Olin ◽  
Nigel E. Hussey ◽  
Alice Grgicak-Mannion ◽  
Mark W. Fritts ◽  
Sabine P. Wintner ◽  
...  

Author(s):  
Stephan Woodborne ◽  
Hannes Botha ◽  
David Huchzermeyer ◽  
Jan Myburgh ◽  
Grant Hall ◽  
...  

2019 ◽  
pp. 389-395 ◽  
Author(s):  
D. Mazzoni ◽  
N. A. Borray-Escalante ◽  
A. Ortega–Segalerva ◽  
L. Arroyo ◽  
J. González–Solís ◽  
...  

Stable isotope analyses (SIAs) have been widely used in recent years to infer the diet of many species. This isotopic approach requires using diet to tissue discrimination factors (DTDFs) for each prey type and predator tissue, i.e., to determine the difference between the isotopic composition of the predator tissues and the different prey that conform its diet. Information on DTDF values in Psittaciformes is scarce. The aim of this study was to assess DTDF values for the carbon and nitrogen isotopes of the monk parakeet (Myiopsitta monachus) and the ring–necked parakeet (Psittacula krameri), two invasive alien species of concern. We fed captive birds of the two parakeet species on a single–species diet based on sunflower seeds to establish the DTDFs for the blood and feathers. In the monk parakeet (N = 9) DTDFs were Δδ13C 2.14 ‰ ± 0.90 and Δδ15N 3.21 ‰ ± 0.75 for the blood, and Δδ13C 3.97 ‰ ± 0.90 and Δδ15N 3.67 ‰ ± 0.74 for the feathers. In the ring–necked parakeet (N = 9), the DTDFs were Δδ13C (‰) 2.58 ± 0.90 and Δδ15N (‰) 2.35 ± 0.78 for the blood, and Δδ13C 3.64 ‰ ± 0.98 and Δδ15N 4.10 ‰ ± 1.84 for the feathers. DTDF values for the ring–necked parakeet blood were significantly higher than those for the monk parakeet blood. No difference was found between the two species in the DTDF for feathers. Our findings provide the first values of DTDFs for blood and feathers in these parakeets, factors that are key to infer the diet of these species based on SIA.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Daniel J. Madigan ◽  
Owyn E. Snodgrass ◽  
John R. Hyde ◽  
Heidi Dewar

AbstractStable isotope analysis (SIA) measurements from long-term captivity studies provide required parameters for interpretation of consumer SIA data. We raised young-of-the-year (14–19 cm) California yellowtail (Seriola dorsalis) on a low δ15N and δ13C diet (pellet aquaculture feed) for 525 days, then switched to a high δ15N and δ13C diet (mackerel and squid) for 753 days. Yellowtail muscle was sequentially sampled from each individual after the diet switch (0 to 753 days) and analyzed for δ15N and δ13C, allowing for calculation of diet-tissue discrimination factors (DTDFs) from two isotopically different diets (low δ15N and δ13C: pellets; high δ15N and δ13C: fish/squid) and turnover rates of 15N and 13C. DTDFs were diet dependent: Δ15N = 5.1‰, Δ13C = 3.6‰ for pellets and Δ15N = 2.6‰, Δ13C = 1.3‰ for fish/squid. Half-life estimates from 15N and 13C turnover rates for pooled yellowtail were 181 days and 341 days, respectively, but varied considerably by individual (15N: 99–239 d; 13C: 158–899 d). Quantifying DTDFs supports isotopic approaches to field data that assume isotopic steady-state conditions (e.g., mixing models for diet reconstruction). Characterizing and quantifying turnover rates allow for estimates of diet/habitat shifts and “isotopic clock” approaches, and observed inter-individual variability suggests the need for large datasets in field studies. We provide diet-dependent DTDFs and growth effects on turnover rates, and associated error around these parameters, for application to field-collected SIA data from other large teleosts.


2012 ◽  
Vol 63 (10) ◽  
pp. 878 ◽  
Author(s):  
J. Veliscek Carolan ◽  
D. Mazumder ◽  
C. Dimovski ◽  
R. Diocares ◽  
J. Twining

Knowledge and understanding of biokinetics and discrimination factors for carbon-13 (δ13C) and nitrogen-15 (δ15N) are important when using stable isotopes for food-web studies. Therefore, we performed a controlled laboratory diet-switch experiment to examine diet–tissue and diet–faeces discrimination factors as well as the biokinetics of stable-isotope assimilation in the omnivorous freshwater crustacean, Cherax destructor. The biokinetics of δ13C could not be established; however, the δ15N value of C. destructor tissue reached equilibrium after 80 ± 35 days, with an estimated biological half-time for 15N of 19 ± 5 days. Metabolic activity contributed to the turnover of 15N by nearly an order of magnitude more than growth. The diet–tissue discrimination factors at the end of the exposure were estimated as –1.1 ± 0.5‰ for δ13C and +1.5 ± 1.0‰ for δ15N, indicating that a δ15N diet–tissue discrimination factor different from the typically assumed +3.4‰ may be required for freshwater macroinvertebrates such as C. destructor. The diet–faeces discrimination factor for δ15N after 120 days was estimated as +0.9 ± 0.5‰. The present study provides an increased understanding of the biokinetics and discrimination factors for a keystone freshwater macroinvertebrate that will be valuable for future food-web studies in freshwater ecosystems.


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