scholarly journals BODY-MASS ESTIMATION IN PALEONTOLOGY: A REVIEW OF VOLUMETRIC TECHNIQUES

2016 ◽  
Vol 22 ◽  
pp. 133-156 ◽  
Author(s):  
Charlotte A. Brassey

AbstractBody mass is a key parameter for understanding the physiology, biomechanics, and ecology of an organism. Within paleontology, body mass is a fundamental prerequisite for many studies considering body-size evolution, survivorship patterns, and the occurrence of dwarfism and gigantism. The conventional method for estimating fossil body mass relies on allometric scaling relationships derived from skeletal metrics of extant taxa, but the recent application of three-dimensional imaging techniques to paleontology (e.g., surface laser scanning, computed tomography, and photogrammetry) has allowed for the rapid digitization of fossil specimens. Volumetric body-mass estimation methods based on whole articulated skeletons are therefore becoming increasingly popular. Volume-based approaches offer several advantages, including the ability to reconstruct body-mass distribution around the body, and their relative insensitivity to particularly robust or gracile elements, i.e., the so-called ‘one bone effect.’ Yet their application to the fossil record will always be limited by the paucity of well-preserved specimens. Furthermore, uncertainties with regards to skeletal articulation, body density, and soft-tissue distribution must be acknowledged and their effects quantified. Future work should focus on extant taxa to improve our understanding of body composition and increase confidence in volumetric model input parameters.

2018 ◽  
Vol 25 (1) ◽  
pp. 17-22
Author(s):  
Karin Booysen ◽  
Johannes Marthinus Dippenaar ◽  
Francois Jacobus Smith

Author(s):  
Erik Trinkaus ◽  
Alexandra P. Buzhilova ◽  
Maria B. Mednikova ◽  
Maria V. Dobrovolskaya

Considerations of the body proportions and estimates of body mass and stature of the Sunghir people provide a general baseline for the assessment of a variety of aspects of their paleobiology. They also furnish some indications by themselves. Some of these aspects have been men­tioned with respect to sexual assessment of the adult remains (especially Sunghir 1 and 4; chapter 6), and methodological considerations have been addressed in part in chapter 5. What is presented here is a more detailed assessment of size in terms of body mass estimation and stature, and considerations of body proportions to the extent that they can be evaluated for Sunghir 1, 2 and 3. Body mass estimation was discussed in chapter 5, and it is done here exclusively using the dimension of the weight-bearing femoral articulations and/or metaphyses. It provides insights into trends in overall body size and health, but it is also central to the appropriate scaling of other aspects of morphology, from limb length and strength to brain size. Since the early comments of Boule (1911–1913) and Coon (1962), there has been a series of attempts to evaluate the body proportions (principally using limb segment lengths but also body breadth and trunk length) of Pleistocene humans as indications of both ecogeographical patterning among Late Pleistocene humans and possible reflections of their population dynamics (e.g., Trinkaus 1981, 2007; Walker and Leakey 1993; Ruff 1994; Holliday 1997a, 1997b, 2000, 2006a; Trinkaus and Zilhão 2002; Frelat 2007). The critical problem in assessing body proportions is to determine the independent variable. This must be done a priori, based on biological considerations. Stature estimation presents a variety of difficulties among Late Pleistocene humans, given variation in linear body proportions, but it can provide an indication of overall health, especially given the trends evident through the European Upper Paleolithic (Formicola and Giannecchini 1999; Holt and Formicola 2008). Assessments of body proportions depend in part on body mass estimation, and stature predictions depend on body proportions.


2021 ◽  
Vol 9 ◽  
Author(s):  
Juha Saarinen ◽  
Omar Cirilli ◽  
Flavia Strani ◽  
Keiko Meshida ◽  
Raymond L. Bernor

The monodactyl horses of the genus Equus originated in North America during the Pliocene, and from the beginning of the Pleistocene, they have been an essential part of the large ungulate communities of Europe, North America and Africa. Understanding how body size of Equus species evolved and varied in relation to changes in environments and diet thus forms an important part of understanding the dynamics of ungulate body size variation in relation to Pleistocene paleoenvironmental changes. Here we test previously published body mass estimation equations for the family Equidae by investigating how accurately different skeletal and dental measurements estimate the mean body mass (and body mass range) reported for extant Grevy's zebra (Equus grevyi) and Burchell's zebra (Equus quagga). Based on these tests and information on how frequently skeletal elements occur in the fossil record, we construct a hierarchy of best practices for the selection of body mass estimation equations in Equus. As a case study, we explore body size variation in Pleistocene European Equus paleopopulations in relation to diet and vegetation structure in their paleoenvironments. We show a relationship between diet and body size in Equus: very large-sized species tend to have more browse-dominated diets than small and medium-sized species, and paleovegetation proxies indicate on average more open and grass-rich paleoenvironments for small-sized, grazing species of Equus. When more than one species of Equus co-occur sympatrically, the larger species tend to be less abundant and have more browse-dominated diets than the smaller species. We suggest that body size variation in Pleistocene Equus was driven by a combined effect of resource quality and availability, partitioning of habitats and resources between species, and the effect of environmental openness and group size on the body size of individuals.


PLoS ONE ◽  
2021 ◽  
Vol 16 (12) ◽  
pp. e0260505
Author(s):  
Jessica Mongillo ◽  
Giulia Vescovo ◽  
Barbara Bramanti

Over the centuries, iconographic representations of St Anthony of Padua, one of the most revered saints in the Catholic world, have been inspired by literary sources, which described the Saint as either naturally corpulent or with a swollen abdomen due to dropsy (i.e. fluid accumulation in the body cavities). Even recent attempts to reconstruct the face of the Saint have yielded discordant results regarding his outward appearance. To address questions about the real appearance of St Anthony, we applied body mass estimation equations to the osteometric measurements taken in 1981, during the public recognition of the Saint’s skeletal remains. Both the biomechanical and the morphometric approach were employed to solve some intrinsic limitations in the equations for body mass estimation from skeletal remains. The estimated body mass was used to assess the physique of the Saint with the body mass index. The outcomes of this investigation reveal interesting information about the body type of the Saint throughout his lifetime.


2014 ◽  
Vol 28 (S1) ◽  
Author(s):  
Go‐Un Jung ◽  
U‐Young Lee ◽  
Dong‐Ho Kim ◽  
Dai‐Soon Kwak ◽  
Yong‐Woo Ahn ◽  
...  

2019 ◽  
Vol 46 (4) ◽  
pp. 334
Author(s):  
Tad M. Bartareau

Context Measuring a mammal’s body mass has importance in understanding nutritional condition, reproductive biology and ecology. It can be impractical for a researcher to measure the body mass when equipment needed to weigh individuals is inadequate or unavailable. Aims The purpose of this study was to develop a model to accurately estimate the body mass of hunter-harvested Florida white-tailed deer (Odocoileus virginianus osceola, Odocoileus virginianus seminolus) based on the relationship between scale mass, sex and standard age and morphometric measurement predictor variables easily obtainable in the field. Methods An information-theoretic approach was used to evaluate simple and multiple linear regression models with 67% of the data, and the best model in the set was validated using the remaining 33%. Key results Chest girth was the best single predictor of body mass. A global model including sex, age, age2 and body length variables was better supported than chest girth alone, and subspecies information did not contribute significantly to the body-mass–predictor-variable relationship. The best model explained 98.5% of the variation in body mass as follows: body mass (kg) = –18.41 + 6.53 × sex (0 = female, 1 = male) + 5.04 × age (year) – 0.49 × age2 (year2) + 4.76 × 10−3 × chest girth2 (cm2) + 0.12 × body length (cm). The 95% confidence interval on the bias of the estimated body mass of the best model was –0.50 to 0.59 kg. The difference between estimated and scale body mass was –0.04 kg ± 0.28 (s.e.). Conclusions Individuals maintained a similar proportion of body mass to predictor variables, and differences between the observed and estimated body mass of model applied to the validation dataset were not significant. Implications The validated body-mass-estimation model presented will enable accurate estimates of the body mass of white-tailed deer in cases where standard age and morphometric measurements are available, but the individuals were not weighed. These results provide a basis to formulate and parameterise body-mass-estimation models for other white-tailed deer subspecies and populations. Without the need for specialised equipment, the body-mass-estimation model can be used by personnel involved in white-tailed deer research, management and sport hunting to assess trends in individual and population health in support of this species’ conservation. Photograph by Carlton Ward Jr.


Paleobiology ◽  
2001 ◽  
Vol 27 (4) ◽  
pp. 735-750 ◽  
Author(s):  
Ryosuke Motani

In computational studies of the body mass and surface area of vertebrates, it is customary to assume that body cross-sections are approximately elliptical. However, a review of actual vertebrate cross-sections establishes that this assumption is not usually met. A new cross-sectional model using superellipses is therefore introduced, together with a scheme that allows estimates to be given with ranges. Tests of the new method, using geometrical shapes, miniature vertebrate models, and actual animals, show that the method has a high accuracy in body mass estimation. A new computer program to perform the computation is introduced. The application of the method to some Mesozoic marine reptiles suggests that the tuna-shaped ichthyosaur Stenopterygius probably had body masses comparable to those of average cetaceans of the same body length.


2012 ◽  
Vol 8 (5) ◽  
pp. 842-845 ◽  
Author(s):  
W. I. Sellers ◽  
J. Hepworth-Bell ◽  
P. L. Falkingham ◽  
K. T. Bates ◽  
C. A. Brassey ◽  
...  

Body mass is a critical parameter used to constrain biomechanical and physiological traits of organisms. Volumetric methods are becoming more common as techniques for estimating the body masses of fossil vertebrates. However, they are often accused of excessive subjective input when estimating the thickness of missing soft tissue. Here, we demonstrate an alternative approach where a minimum convex hull is derived mathematically from the point cloud generated by laser-scanning mounted skeletons. This has the advantage of requiring minimal user intervention and is thus more objective and far quicker. We test this method on 14 relatively large-bodied mammalian skeletons and demonstrate that it consistently underestimates body mass by 21 per cent with minimal scatter around the regression line. We therefore suggest that it is a robust method of estimating body mass where a mounted skeletal reconstruction is available and demonstrate its usage to predict the body mass of one of the largest, relatively complete sauropod dinosaurs: Giraffatitan brancai (previously Brachiosaurus ) as 23200 kg.


Author(s):  
Kathy Yu

Inflammatory bowel diseases (IBD) is severe inflammation of the gastrointestinal tract. This can lead to a breakdown of mucosal barriers, causing dissemination of commensal bacteria throughout the body. To better understand bacterial translocation during IBD, aim to develop a fluorescent microbiota in mice that we can interrogate using live imaging techniques.   Our preliminary experiments depleted commensals using broad-spectrum antibiotics,  and replaced these microbiota with a fluorescent E. coli strain. The length of time that E.coli stays in the mice gut were monitored. We show that E. coli can persist in the ‘germ-free’ mouse gut for at least 21 days; control mice lose all added E. coli by 8-14 days. The establishment of the E. coli colony suggests this could be a reasonable model to study bacterial translocation.  We are currently going to treat the colonized mice with DSS to induce colitis, and then to study translocation of E. coli by intravital microscopy. Considering E. coli is only a fraction of the normal microbiota and perhaps not a relevant model, future work aims at making a fluorescent microbiota consisting of multiple endogenous murine microbes. This will entail the use of a bacterial conjugation system  capable of ubiquitously transforming many microbial species.  


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