Changes in isotopic composition of red drum (Sciaenops ocellatus) larvae in response to dietary shifts: potential applications to settlement studies
193 citations recorded by the source corpus.
Subfields: Ecology, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/0c43d25f6903a72b2eebae48762f3eb1bcc10d1e
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Citations in the corpus
- Tissue-specific turnover rates of the nitrogen stable isotope as functions of time and growth in a cyprinid fish (2018, background): “This also raises some caution as to the applicability of these predictions to older life-stages, where individuals are likely to be slower growing and sexually mature (Hesslein et al., 1993; Herzka & Holt, 2000; Perga & Gerdeaux, 2005).”
- Sources of variation in consumer-diet δ15N enrichment: a meta-analysis (2003, background): “... Yeast 3.50 0.01 I Whole body H UA Roth and Hobson 2000 Vulpes vulpes (red fox) Pellet food 2.60 0.12 M Plasma M U Roth and Hobson 2000 Vulpes vulpes (red fox) Pellet food 3.20 0.12 M Red blood cells M U Roth and Hobson 2000 Vulpes vulpes (red fox) Pellet food 3.30 0.11 M Liver M U Roth and Hobso”
- Experimental evaluation of stable isotope fractionation in fish muscle and otoliths (2010, background): “Stable isotopes provide integrated esti- mates of diet over time that can be used to infer longerterm feeding behaviour and movements (Hobson & Wassenaar 1999, Herzka & Holt 2000, Haas et al. 2009).”
- Isotopic turnover in aquatic predators: quantifying the exploitation of migratory prey (2001, background): “Herzka and Holt (2000) found rapid turnover of 13C and 15N in red drum larvae, which generally matched the very high growth rate of these very young fish (doubling of biomass occurred in 1 or 2 days).”
- Growth versus metabolic tissue replacement in mouse tissues determined by stable carbon and nitrogen isotope analysis (2005, background): “, 1758)) (Hobson and Clark 1992a, 1992b), or larval/juvenile fish (Herzka and Holt 2000; Harvey et al. 2002).”
- Stable isotopes in jumbo squid (Dosidicus gigas) beaks to estimate its trophic position: comparison between stomach contents and stable isotopes (2006, methodology): “Isotopic shift predictions Isotopic shifts in fast growing organisms can be described based on a simple dilution model (no metabolic turnover e¡ect; c¼71) using the equation of Fry & Arnold (1982) and based on growth rate estimates for natural populations (Herzka & Holt, 2000; Herzka 2005).”
- Assessing connectivity of estuarine fishes based on stable isotope ratio analysis (2005, background): “Previous studies indicate that equilibrium to a new food source will be approached after a four- to six-fold increase in biomass (Herzka and Holt, 2000; Bosley et al., 2002; Harvey et al., 2002).”
- Estimating turnover rates of carbon and nitrogen in recently metamorphosed winter flounder Pseudopleuronectes americanus with stable isotopes (2002, unknown): “Recent studies have used stable isotopes to examine food-web interactions and fish migration (Hansson et al. 1997) and to document the settlement history of individual fish larvae into demersal habitats (Herzka et al. 2001).”
- A non-lethal sampling method for stable carbon and nitrogen isotope studies of tropical fishes (2011, unknown): “1993) rather than the days to weeks observed for rapidly growing juvenile fish (Herzka and Holt 2000).”
- Changes in d13C and d15N in different tissues of juvenile sand goby Pomatoschistus minutus: a laboratory diet-switch experiment (2007, background): “…and predictable (Maes et al. 2004), the utilization of stable isotopes as tracers of individual recruitment to the estuary will reveal the migration dynamics on a finer temporal scale, thereby improving our understanding of the life history strategies of marine fish species (Herzka & Holt 2000).”
- Trophic ecology of Sargassum-associated fishes in the Gulf of Mexico determined from stable isotopes and fatty acids (2006, result): “…values for Sargassum (2.5 to 2.8‰) compared well with measurements reported by Moncrieff & Sullivan (2001), and our mean δ15N value of 7.1‰ for phytoplankton was similar to values (7 to 9‰) reported in other studies conducted in the Gulf of Mexico (Sullivan & Moncreiff 1990, Herzka & Holt 2000).”
- Variable uptake and elimination of stable nitrogen isotopes between tissues in fish (2006, background): “Conversely, several authors found that high metabolic rates also appear capable of elevating muscular δ15N signatures (Herzka and Holt 2000; Gaye-Siessegger et al. 2004).”
- Multi-species larval fish growth model based on temperature and fluorometrically derived RNA/DNA ratios: results from a meta-analysis (2008, methodology): “…of W = 0.0128(Lcm)3 (where Lcm = length in centimeters) (Kondo et al. 1976 cited by Suda & Kishida 2003) was used to convert growth-in-length data to growth-in-weight for the 2 Japanese sardine studies, and a length exponent of 3.3 (Herzka & Holt 2000) was used for the 2 red drum studies (Table 2).”
- Rates and components of carbon turnover in fish muscle: insights from bioenergetics models and a whole-lake 13C addition (2011, background): “(8C) Mass (g) Study Red drum (Sciaenops ocellatus) 0.1150 6.0 28.00 2.40 10–5 Herzka and Holt 2000*,{ 0.1380 5.0 28.00 7.40 10–4 Herzka and Holt 2000*,{ 0.0990 7.0 24.00 8.90 10–4 Herzka and Holt 2000*,{ Channel catfish (Icatalurus punctatus) 0.0140 49.5 15.00 8.67 101 MacAvoy et al. 2001 Winter…”
- Differential isotopic enrichment and half-life among tissues in Japanese temperate bass (Lateolabrax japonicus) juveniles: implications for analyzing migration (2005, background): “5-year-old broad whitefish (Coregonus nasus) (Hesslein et al. 1993) and 5.0–17.3 days for juvenile Japanese flounder (Paralichthys olivaceus) (calculated from the original data of the turnover rate; Tominaga et al. 2003). As for the HLmuscle values of δ15N, although there are no data available from ”