Using bioenergetics models to predict stable isotope ratios in fishes

By C. Harvey, Paul C. Hanson, T. Essington, P. Brown, J. Kitchell. 2002

134 citations recorded by the source corpus.

Subfields: Ecology, Global and Planetary Change, Nature and Landscape Conservation

View Paper: https://www.semanticscholar.org/paper/67d273e736144333dca83ba535c163bc18f7856e

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology

1. A. Fisk
2. M. Vanderklift
3. L. Arneson
4. D. Schindler
5. S. Chipps
6. D. Wahl
7. J. Kitchell
8. A. Tobin

In Global and Planetary Change

1. D. Schindler
2. A. Fisk
3. Stephen R. Carpenter
4. J. Moore
5. D. Wahl
6. S. Chipps
7. J. Kitchell
8. M. Vanderklift

In Nature and Landscape Conservation

1. Stephen R. Carpenter
2. A. Tobin
3. J. Kitchell
4. J. Moore
5. D. Wahl
6. S. Chipps
7. A. Fisk
8. M. Kinney

Citations in the corpus

• Assessing connectivity of estuarine fishes based on stable isotope ratio analysis (2005, background): “The effect of varying environmental conditions on turnover rates could be accounted for through the integration of bioenergetic principles into models of isotopic turnover (Harvey et al., 2002).”
• Energy Density of Patagonian Aquatic Organisms and Empirical Predictions Based on Water Content (2007, methodology): “Bioenergetics models have also been used to investigate environmental problems, such as the potential effects of fish introductions (Ruzycki et al. 2003), global warming (Hill and Magnuson 1990), predation as a factor in recruitment failure (Hartman and Margraf 1993), and other issues in fish ecolog”
• Bioenergetics Modeling in the 21st Century : Reviewing New Insights and Revisiting Old Constraints (2008, methodology): “The recent symposium organized by Hartman et al. (this issue) highlighted the diversity of models being developed and the increased number of ways in which these models are being used (e.g., Petersen and Kitchell 2001; Trudel et al. 2001; Harvey et al. 2002).”
• Communal or competitive? Stable isotope analysis provides evidence of resource partitioning within a communal shark nursery (2011, background): “…food webs (Hobson & Welch 1992, Michener & Schell 1994, Hobson et al. 2002), and focusing on specific teleost species (Thomas & Cahoon 1993, Das et al. 2000, Harvey et al. 2002, Cunjak et al. 2005, Perga & Gerdeaux 2005, Schlacher et al. 2005), little research has been published on SIA for sharks.”
• Rates and components of carbon turnover in fish muscle: insights from bioenergetics models and a whole-lake 13C addition (2011, background): “An alternative approach to estimating isotopic rates of change uses daily fish growth and consumption estimates from bioenergetic models paired with isotopic time series of fish tissue and diet (Harvey et al. 2002).”
• Variable uptake and elimination of stable nitrogen isotopes between tissues in fish (2006, background): “Finally, Harvey et al. (2002) estimated m in juvenile lake trout (Salvelinus namaycush) muscle to be 0.”
• Stable isotopes from multiple tissues reveal diet switching in sharks (2005, background): “Mako sharks from south of Martha’s Vineyard are part of a northwest Atlantic population that has distinct inshore (on shelf) and offshore (off shelf) feeding groups (Stillwell & Kohler 1982, Heist et al. 1996).”
• Stable isotopes (δ13C, δ15N) and modelling as tools to estimate the trophic ecology of cultivated oysters in two contrasting environments (2007, methodology): “…with an estimation of the turnover rate of the whole oyster tissues to take into account the incorporation rate of the OMS through a dynamic energy budget (DEB) model developed for this species (Pouvreau et al. 2006), as recently experienced with bioenergetics model on fishes (Harvey et al. 2002).”
• Sources of variation in consumer-diet δ15N enrichment: a meta-analysis (2003, background): “... (spider) Rhopalosiphum padi 1.50 0.10 S Whole body C G 8.3 Oelbermann and Scheu 2002 Heteromurus nitidus (collembolan) Yeast 1 5.19 0.49 I Whole body H UA Oelbermann and Scheu 2002 Folsomia candida (collembolan) Yeast 2 4.54 0.57 I Whole body H UA Oelbermann and Scheu 2002 Drosophila melanogaste”
• Growth versus metabolic tissue replacement in mouse tissues determined by stable carbon and nitrogen isotope analysis (2005, background): “…have been conducted on quickly growing invertebrates (Fry and Arnold 1982; Frazer et al. 1997), Japanese quail (Coturnix japonica Temminck and Schlegel, 1849) and chickens (Gallus gallus (L., 1758)) (Hobson and Clark 1992a, 1992b), or larval/juvenile fish (Herzka and Holt 2000; Harvey et al. 2002).”
• Varying effects of anadromous sockeye salmon on the trophic ecology of two species of resident salmonids in southwest Alaska (2007, background): “related to trophic level, tissue turnover times and growth rates (Harvey et al., 2002; Miller, 2006).”