Stable isotope composition of walleye: 15N accumulation with age and area-specific differences in δ13C

2001 ◽  
Vol 58 (6) ◽  
pp. 1253-1260 ◽  
Author(s):  
Nathanael C Overman ◽  
Donna L Parrish
Keyword(s):  
Stable Isotope ◽  
Isotopic Composition ◽  
Carbon Isotope ◽  
Trophic Position ◽  
Isotope Composition ◽  
Isotope Analysis ◽  
Isotopic Fractionation ◽  
Stomach Content Analysis ◽  
Metabolic Effects ◽  
N Accumulation

Stable nitrogen and carbon isotope ratios were measured for walleye (Stizostedion vitreum) collected across Lake Champlain, Vermont, to determine relationships between isotopic composition and diet, location of capture, length, weight, and age. Variation in δ13C values reflected area-specific differences in isotopic composition of organisms collected across the lake. A critical assumption in the application of isotope techniques is that a predictable relationship exists between the diet and isotopic composition of an organism. Our results indicate that isotopic fractionation factors may not be independent of age as has largely been assumed. By combining stable nitrogen and carbon isotope analysis with conventional stomach content analysis, we documented significant age effects in the δ15N composition of adult walleye that were not attributable to observed changes in diet. Age accounted for 81% of the variation in δ15N values of walleye (ages 2–27, N = 65, δ15N range = 15.3–19.2‰), providing evidence supporting 15N accumulation over the life span of walleye. Therefore, the risk of making faulty inferences of trophic position and food web interactions based on δ15N values may be increased when age is unknown. Our results indicate that metabolic effects associated with age require greater consideration in applications of stable isotope analysis.

Stable carbon isotope analysis of faecal and blood samples of sheep in relation to the diet

2003 ◽  
Vol 2003 ◽  
pp. 159-159
Author(s):  
A. Balcaen ◽  
E. Claeys ◽  
V. Fievez ◽  
P. Boeckx ◽  
O. van Cleemput ◽  
...  
Keyword(s):  
Isotopic Composition ◽  
Carbon Isotope ◽  
Carbon Fixation ◽  
Isotope Composition ◽  
Stable Carbon Isotope ◽  
Isotope Analysis ◽  
Calvin Cycle ◽  
Isotopic Fractionation ◽  
Woody Species ◽  
Stable Carbon

Stable isotopes have been extraordinarily helpful in understanding animal migration, diet, food webs and nutrient flow (Hilderbrand et al., 1996), based on the property that C3 and C4 plants possess distinctly different 13C/12C ratios (δ13C value) due to isotopic fractionation during photosynthetic carbon fixation (Smith & Epstein, 1971). Most woody species and temperate graminoids assimilate carbon via the Calvin cycle (C3), which discriminates stronger against the heavier isotope (13C) than Hatch-Slack (C4) species (tropical and subtropical graminoids and some shrubs). C3 and C4 plant species have mean δ13C values of -27 ‰ and -13 ‰ respectively (O’Leary, 1981). DeNiro & Epstein (1978) were one of the first to show that the isotopic composition of the whole animal body is similar to that of its diet. Other authors have also found relationships between the isotopic composition of animal tissues and the diet (González-Martin et al., 1999; Jones et al., 1979). The aim of this study was to investigate stable carbon isotope composition in sheep fed diets consisting of either C3 or C3+C4 plants.

Preparation of aqueous fatty acids for hydrogen and carbon stable isotope analysis by solid phase extraction

2013 ◽  
Vol 64 (4) ◽  
pp. 294 ◽  
Author(s):  
Timothy J. Benbow ◽  
Alan R. Hayman ◽  
Robert Van Hale ◽  
Russell Frew
Keyword(s):  
Fatty Acids ◽  
Stable Isotope ◽  
Solid Phase Extraction ◽  
Natural Waters ◽  
Solid Phase ◽  
Isotope Composition ◽  
Isotope Analysis ◽  
Isotopic Fractionation ◽  
Phase Extraction ◽  
Surface Modified

Stable isotope analyses of fatty acids in environmental waters provides important information as to their source(s). Analysis is often confounded due to low concentrations of fatty acids and/or a complex sample matrix requiring separation of the target analyte. The purpose of this study was to validate a method to extract fatty acids from natural waters using solid phase extraction (SPE) before compound specific isotope analysis (CSIA). Three SPE cartridges and multiple eluting solvents were tested to determine the efficiency, isotopic fractionation, and reproducibility of each extraction technique. Our results indicated that surface-modified styrene divinylbenzene cartridges, when eluted with methanol, caused negligible fractionation of the hydrogen isotopes and minimal fractionation of the carbon isotopes, but that isotopic fractionation occurred when compounds were only partially eluted from SPE cartridges. Compounds were also extracted from landfill leachate using both SPE and liquid–liquid extraction (LLE). The hydrogen isotope composition (δ2H) of compounds extracted from water using either method were within experimental precision and the carbon isotope composition (δ13C) of all but one fatty acid were within experimental precision. Therefore, these experiments prove the aforementioned SPE methods to be a convenient and precise method to extract fatty acids from natural waters before CSIA.

scholarly journals Stratospheric carbon isotope fractionation and tropospheric histories of CFC-11, CFC-12 and CFC-113 isotopologues

2020 ◽  
Author(s):  
Max Thomas ◽  
Johannes C. Laube ◽  
Jan Kaiser ◽  
Samuel Allin ◽  
Patricia Martinerie ◽  
...  
Keyword(s):  
Isotopic Composition ◽  
Carbon Isotope ◽  
Ozone Depletion ◽  
Isotope Composition ◽  
Stratospheric Ozone ◽  
Isotopic Fractionation ◽  
Base Case ◽  
Model Base ◽  
The Difference ◽  
First Time

Abstract. We present novel measurements of the carbon isotope composition of CFC-11 (CCl3F), CFC-12 (CCl2F2), and CFC-113 (CF2ClCFCl2), three atmospheric trace gases that are important for both stratospheric ozone depletion and global warming. These measurements were carried out on air samples collected in the stratosphere – the main sink region for these gases – and on air extracted from deep polar firn snow. We quantify, for the first time, the apparent isotopic fractionation, εapp(13C), for these gases as they are destroyed in the high- and mid-latitude stratosphere: εapp(CFC-12, high-lat) = (−20.2 ± 4.4) ‰ and εapp(CFC-113, high-lat) = (−9.4 ± 4.4) ‰, εapp(CFC-12, mid-lat) = (−30.3 ± 10.7) ‰, and εapp(CFC-113, mid-lat) = (−34.4 ± 9.8) ‰. Our CFC-11 measurements were not sufficient to calculate εapp(CFC-11) so we instead used previously reported photolytic fractionation for CFC-11 and CFC-12 to scale our εapp(CFC-12), resulting in εapp(CFC-11, high-lat) = (−7.8 ± 1.7) ‰ and εapp(CFC-11, mid-lat) = (−11.7 ± 4.2) ‰. Measurements of firn air were used to construct histories of the tropospheric isotopic composition, δT(13C), for CFC-11 (1950s to 2009), CFC-12 (1950s to 2009), and CFC-113 (1970s to 2009) – with δT(13C) increasing for each gas. We used εapp(high-lat), which were derived from more data, and a constant isotopic composition of emissions, δE(13C), to model δT(13C, CFC-11), δT(13C, CFC-12), and δT(13C, CFC-113). For CFC-11 and CFC-12, modelled δT(13C) was consistent with measured δT(13C) for the entire period covered by the measurements, suggesting no dramatic change in δE(13C, CFC-11) or δE(13C, CFC-12) has occurred since the 1950s. For CFC-113, our modelled δT(13C, CFC-113) did not agree with our measurements earlier than 1980. While this discrepancy may be indicative of a change in δE(13C, CFC-113), it is premature to assign one. Our modelling predicts increasing δT(13C, CFC-11), δT(13C, CFC-12), and δT(13C, CFC-113) into the future. We investigated the effect of recently reported new CFC-11 emissions on background δT(13C, CFC-11) by fixing model emissions after 2012, and comparing δT(13C, CFC-11) in this scenario to the model base case. The difference in δT(13C, CFC-11) between these scenarios was 1.4 ‰ in 2050. This difference is smaller than our model uncertainty envelope and would therefore require improved modelling and measurement precision, as well as better quantified isotopic source compositions, to detect.

scholarly journals Microbial Isotopic Fractionation of Perchlorate Chlorine

2003 ◽  
Vol 69 (8) ◽  
pp. 4997-5000 ◽  
Author(s):  
Max L. Coleman ◽  
Magali Ader ◽  
Swades Chaudhuri ◽  
John D. Coates
Keyword(s):  
Stable Isotope ◽  
Environmental Samples ◽  
Microbial Respiration ◽  
Isotope Composition ◽  
Isotopic Fractionation ◽  
Stable Isotope Composition ◽  
Biotic Degradation ◽  
Chlorine Stable Isotope

ABSTRACT Perchlorate contamination can be microbially respired to innocuous chloride and thus can be treated effectively. However, monitoring a bioremediative strategy is often difficult due to the complexities of environmental samples. Here we demonstrate that microbial respiration of perchlorate results in a significant fractionation (∼−15‰) of the chlorine stable isotope composition of perchlorate. This can be used to quantify the extent of biotic degradation and to separate biotic from abiotic attenuation of this contaminant.

Paleodietary Patterns of the Cherepakha 13 Site Population (Early Iron Age) in Primorye (Maritime) Province, Russian Far East, based on Stable Isotope Analysis

Radiocarbon ◽  
2018 ◽  
Vol 60 (5) ◽  
pp. 1611-1620 ◽  
Author(s):  
Yaroslav V Kuzmin ◽  
Vsevolod S Panov ◽  
Viacheslav V Gasilin ◽  
Sergei V Batarshev
Keyword(s):  
Stable Isotope ◽  
Iron Age ◽  
Isotope Composition ◽  
Russian Far East ◽  
Isotope Analysis ◽  
Far East ◽  
Bone Collagen ◽  
Early Iron Age ◽  
Terrestrial Mammals ◽  
Maritime Province

ABSTRACTNew paleodietary data were obtained after the discovery and excavation in 2015–2017 of the Cherepakha 13 site in the southern part of Primorye (Maritime) Province in far eastern Russia. The site is located near the coast of Ussuri Bay (Sea of Japan) and belongs to the Yankovsky cultural complex of the Early Iron Age 14C-dated to ca. 3000 BP (ca. 1200 cal BC). The stable isotope composition of the bone collagen for 11 humans and 30 animals was determined. For humans, the following values (with±1 sigma) were yielded: δ13C=–10.2±0.8‰; and δ15N=+12.4±0.3‰. The majority of terrestrial animals show the usual isotopic signals: δ13C=–19.4 ÷ –23.3‰; and δ15N=+4.6÷+6.6‰ (for wolves, up to +10.1‰); dogs, however, have an isotopic composition similar to humans: δ13C= –11.7±1.2‰; and δ15N=+12.4±0.4‰. Marine mammals have common values for pinnipeds: δ13C=–13.7 ÷ –14.6‰; and δ15N=+17.4 ÷ +18.0‰. The main food resources for the population of Cherepakha 13 site were (1) marine mollusks, fish, and mammals; and (2) terrestrial mammals; and possibly C4 plants (domesticated millets).

scholarly journals Stable Oxygen and Carbon Isotope Composition of Holocene Mytilidae from the Camarones Coast (Chubut, Argentina): Palaeoceanographic Implications

Water ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3464
Author(s):  
Gabriella Boretto ◽  
Giovanni Zanchetta ◽  
Ilaria Consoloni ◽  
Ilaria Baneschi ◽  
Massimo Guidi ◽  
...  
Keyword(s):  
Stable Isotope ◽  
Carbon Isotope ◽  
Isotope Composition ◽  
Temperature Shift ◽  
Carbon Isotope Composition ◽  
Isotopic Shift ◽  
Stable Isotope Composition ◽  
Oxygen And Carbon Isotope ◽  
Stable Oxygen ◽  
Southern Westerlies

The stable isotope composition of living and of Holocene Mytilidae shells was measured in the area of Camarones (Chubut, Argentina). The most striking results were the high δ18O values measured in samples older than ca. 6.1 cal ka BP. In the younger samples, the δ18O values remained substantially stable and similar to those of living specimens. Analysis of the data revealed the possibility for this isotopic shift to be driven mainly by changes in temperature probably accompanied by minor changes in salinity, suggesting cooler seawater before 6.1 cal ka BP, with a maximum possible temperature shift of ca. 5 °C. A possible explanation of this change can be related to a northward position of the confluence zone of the Falkland and Brazilian currents. This is consistent with the data obtained in marine cores, which indicate a northerly position of the confluence in the first half of the Holocene. Our data are also in line with the changes in wind strength and position of the Southern Westerlies Wind, as reconstructed in terrestrial proxies from the Southernmost Patagonia region.

scholarly journals <sup>2</sup>H and <sup>18</sup>O depletion of water close to organic surfaces

2016 ◽  
Vol 13 (10) ◽  
pp. 3175-3186 ◽  
Author(s):  
Guo Chen ◽  
Karl Auerswald ◽  
Hans Schnyder
Keyword(s):  
Isotopic Composition ◽  
Soil Water ◽  
Filter Paper ◽  
Surface Effect ◽  
Isotope Composition ◽  
Isotopic Fractionation ◽  
Adsorbed Water ◽  
Organic Soil ◽  
Surface Areas ◽  
Isotope Composition Of Water

Abstract. Hydrophilic surfaces influence the structure of water close to them and may thus affect the isotope composition of water. Such an effect should be relevant and detectable for materials with large surface areas and low water contents. The relationship between the volumetric solid : water ratio and the isotopic fractionation between adsorbed water and unconfined water was investigated for the materials silage, hay, organic soil (litter), filter paper, cotton, casein and flour. Each of these materials was equilibrated via the gas phase with unconfined water of known isotopic composition to quantify the isotopic difference between adsorbed water and unconfined water. Across all materials, isotopic fractionation was significant (p<0.05) and negative (on average −0.91 ± 0.22 ‰ for 18∕16O and −20.6 ± 2.4 ‰ for 2∕1H at an average solid : water ratio of 0.9). The observed isotopic fractionation was not caused by solutes, volatiles or old water because the fractionation did not disappear for washed or oven-dried silage, the isotopic fractionation was also found in filter paper and cotton, and the fractionation was independent of the isotopic composition of the unconfined water. Isotopic fractionation became linearly more negative with increasing volumetric solid : water ratio and even exceeded −4 ‰ for 18∕16O and −44 ‰ for 2∕1H. This fractionation behaviour could be modelled by assuming two water layers: a thin layer that is in direct contact and influenced by the surface of the solid and a second layer of varying thickness depending on the total moisture content that is in equilibrium with the surrounding vapour. When we applied the model to soil water under grassland, the soil water extracted from 7 and 20 cm depth was significantly closer to local meteoric water than without correction for the surface effect. This study has major implications for the interpretation of the isotopic composition of water extracted from organic matter, especially when the volumetric solid : water ratio is larger than 0.5 or for processes occurring at the solid–water interface.

scholarly journals Stable Isotopes (H, C, S) and the Origin of Baltic Amber

2009 ◽  
Vol 33 (-1) ◽  
pp. 33-36 ◽  
Author(s):  
Algirdas Gaigalas ◽  
Stanislaw Halas
Keyword(s):  
Stable Isotopes ◽  
Carbon Isotope ◽  
Isotope Composition ◽  
Isotope Analysis ◽  
Carbon Isotope Composition ◽  
Baltic Amber ◽  
Light Elements ◽  
Subsequent Evolution

Stable Isotopes (H, C, S) and the Origin of Baltic Amber New results of isotope analysis of light elements (H, C and S) of a dozen Baltic amber samples are described and discussed. Carbon isotope composition was nearly constant (ca. -23‰), whereas sulphur and hydrogen varied in their isotope compositions from +4 to -28‰ and from -171 to -213‰, respectively. The formation and subsequent evolution of this material since its origin in Paleogene time until present is outlined.

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