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      Quantitative Units and Terminology in Zooarchaeology

      American Antiquity
      JSTOR

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          Abstract

          Fifteen years ago Casteel and Grayson (1977) identified potential ambiguity in the definitions of quantitative terms and units used by zooarchaeologists. As solutions they suggested that analysts use the original definitions of terms and explicitly specify how units are counted. The history of zooarchaeology since then has involved a shift from producing estimates of taxonomic abundances to measuring various taphonomic processes and effects within taxa. As a result, many new quantitative units and terms for those units have been proposed. Some of these new units and terms have been used to measure properties of bone assemblages that are not clearly related to a taphonomic process or effect. Other units and terms have been used inappropriately due to apparent misunderstanding of the property measured by a unit or due to some assumed, implicit meaning of a term. The 112 terms compiled for this study have 122 distinct definitions. Some of the designated quantitative units are synonymous with one another while other units are used in ambiguous manners that seriously compromise their reliability. Explicit definitions of quantitative units and terms along with detailed descriptions of how individual units are measured are mandatory to the efficient communication of research results and the continued prosperity of zooarchaeological research.

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          Most cited references59

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          Systematic Butchery by Plio/Pleistocene Hominids at Olduvai Gorge, Tanzania [and Comments and Reply]

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            Bone density and differential survivorship of fossil classes

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              Impact of Carnivore Ravaging on Zooarchaeological Measures of Element Abundance

              Most zooarchaeologists estimate limb-bone abundance from limb ends. Researchers have provided detailed documentation of the preferential destruction by carnivores of limb ends (Binford 1981; Binford et al. 1988; Blumenschine 1988; Brain 1981; Marean et al. 1990; Orloff and Marean 1990; Sutcliffe 1970). Others have observed differences between limb abundances calculated on limb shafts vs. ends, suggesting shaft pieces may provide more accurate estimates of original element abundance in carnivore-ravaged assemblages (Bunn 1986; Bunn and Kroll 1986; Blumenschine 1988; Klein 1975; Marean et al. 1990; Orloff and Marean 1990). However, the exact quantitative effect of carnivore ravaging on measures of element abundance has never been investigated. We provide an experimental test of the accuracy of different bone portions for estimating the original element abundance after carnivore ravaging. Spotted hyenas were allowed to ravage 33 simulated archaeological sites of known element abundance. Estimates of abundance calculated on limb ends differ greatly from original bone abundance, and estimates based on proximal/distal-shaft pieces are also inaccurate. Estimates from middle-shaft fragments, however, are uniquely accurate. These experimental data mandate reanalysis of assemblages where limb frequencies were calculated from limb ends and carnivore ravaging is implicated, and experimentally vindicate observations originally provided by Klein (1975).
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                Author and article information

                Journal
                applab
                American Antiquity
                American Antiquity
                JSTOR
                0002-7316
                January 1994
                January 2017
                : 59
                : 01
                : 36-71
                Article
                10.2307/3085500
                e65d3a6d-3543-4cd4-b2a8-a3eec681c22f
                © 1994
                History

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