2001
DOI: 10.1080/00241160152418401
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Application of trophic transfer efficiency and age structure in the trophic analysis of fossil assemblages

Abstract: 2001 06 15: Application of trophic transfer ef ciency and age structure in the trophic analysis of fossil assemblages. Lethaia, Vol. 34, pp. 97-118. Oslo. ISSN 0024-1164. We evaluate onshore-offshore trends in age-frequency distributions and trophic transfer ef ciencies using 11 modern death assemblages off the Texas coast. Trophic transfer ef ciencies within trophic levels offer little insight over that achieved by a size-frequency distribution. Production/biomass ratios will always be 1 in the fossil reco… Show more

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Cited by 10 publications
(5 citation statements)
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“…5B). Because energy from primary pro duction is transferred inefficiently through primary consumers before being consumed by carnivores, the net primary production (NPP) ultimately required to support a carnivore is far greater than that required to sustain a primary consumer of the same size (Kerr and Dickie 2001;Powell et al 2001). al.…”
Section: Sizementioning
confidence: 99%
“…5B). Because energy from primary pro duction is transferred inefficiently through primary consumers before being consumed by carnivores, the net primary production (NPP) ultimately required to support a carnivore is far greater than that required to sustain a primary consumer of the same size (Kerr and Dickie 2001;Powell et al 2001). al.…”
Section: Sizementioning
confidence: 99%
“…The fossil record provides direct evidence of long-term changes in ecosystem structure, but accurately interpreting this evidence can be challenging due to taphonomic biases and the inability to directly measure many critical properties of ecosystems. In particular, secular trends in biomass and energy consumption may be intimately linked to global trends in biodiversity, paleoecology, and geochemical cycles (e.g., Bambach 1993; Vermeij 1995; Bush and Bambach 2011; Allmon and Martin 2014; Knoll and Follows 2016), but these trends have only recently been the focus of quantitative paleontological study due to the challenges inherent in interpreting them from the fossil record (Finnegan and Droser 2008; Finnegan et al 2011; Bush et al 2013; Finnegan 2013; Payne et al 2014; see also Powell and Stanton 1985, 1996; Staff et al 1985; Powell et al 2001).…”
Section: Introductionmentioning
confidence: 99%
“…These factors include pre servational taphonomic biases (postmortem distortion of species' relative abundances arising from differential preservation of spe cies and age classes or out-of-habitat trans portation), the time-averaging of naturally variable populations (which lengthens the window of observation on local community composition), and "supply-side" taphonomic biases such as differential turnover of popu lations among species, affecting their contri bution of dead individuals. Of these potential factors, life span bias-the expected overrepresentation in time-averaged death assem blages of species whose individuals have short life spans-has long been suspected to significantly distort species' relative abun dances but has received little analytic atten tion (Van Valen 1964;Levinton and Bambach 1969;Levinton 1970;Behrensmeyer and Chapman 1993;Callender and Powell 1997;Powell et al 2001;Vermeij and Herbert 2004;Tomasovych 2004).…”
Section: Introductionmentioning
confidence: 99%