Commentary on the Article “Interpreting Aerobic Fitness in Youth: The Fallacy of Ratio Scaling”—Is Body Mass the Best Body Size Descriptor to Normalize Aerobic Fitness in the Pediatric Population?

2019 ◽  
Vol 31 (3) ◽  
pp. 386-387 ◽  
Author(s):  
Giovani dos Santos Cunha ◽  
Gabriela Tomedi Leites
Keyword(s):  
Body Size ◽  
Body Mass ◽  
Aerobic Fitness ◽  
Pediatric Population ◽  
Size Descriptor ◽  
Ratio Scaling

scholarly journals The Development of Aerobic and Anaerobic Fitness with Reference to Youth Athletes

2020 ◽  
Vol 2 (4) ◽  
pp. 275-286 ◽  
Author(s):  
Neil Armstrong ◽  
Jo Welsman
Keyword(s):  
Longitudinal Data ◽  
Body Mass ◽  
Aerobic Fitness ◽  
Power Output ◽  
Fat Free Mass ◽  
Peak Power Output ◽  
Youth Athletes ◽  
Physiological Variables ◽  
Aerobic And Anaerobic ◽  
Ratio Scaling

Abstract Purpose To challenge current conventions in paediatric sport science and use data from recent longitudinal studies to elucidate the development of aerobic and anaerobic fitness, with reference to youth athletes. Methods (1) To critically review the traditional practice of ratio scaling physiological variables with body mass and, (2) to use multiplicative allometric models of longitudinal data, founded on 1053 (550 from boys) determinations of 10–17-year-olds’ peak oxygen uptake ($$ {{\text{V}}\text{O}}_{2} $$ VO 2 ) and 763 (405 from boys) determinations of 11–17-year-olds’ peak power output (PP) and mean power output (MP), to investigate the development of aerobic and anaerobic fitness in youth. Results The statistical assumptions underpinning ratio scaling of physiological variables in youth are seldom met. Multiplicative allometric modelling of longitudinal data has demonstrated that fat free mass (FFM) acting as a surrogate for active muscle mass, is the most powerful morphological influence on PP, MP, and peak $$ {{\text{V}}\text{O}}_{2} $$ VO 2 . With FFM appropriately controlled for, age effects remain significant but additional, independent effects of maturity status on anaerobic and aerobic fitness are negated. Conclusions Ratio scaling of physiological variables with body mass is fallacious, confounds interpretation of the development of anaerobic and aerobic fitness, and misleads fitness comparisons within and across youth sports. Rigorous evaluation of the development of anaerobic and aerobic fitness in youth requires longitudinal analyses of sex-specific, concurrent changes in age- and maturation-driven morphological covariates. Age and maturation-driven changes in FFM are essential considerations when evaluating the physiological development of youth athletes.

Allometric scaling of peak oxygen uptake in male roller hockey players under 17 years old

2013 ◽  
Vol 38 (4) ◽  
pp. 390-395 ◽  
Author(s):  
João Valente-dos-Santos ◽  
Lauren Sherar ◽  
Manuel J. Coelho-e-Silva ◽  
João R. Pereira ◽  
Vasco Vaz ◽  
...  
Keyword(s):  
Body Size ◽  
Oxygen Uptake ◽  
Body Mass ◽  
Peak Oxygen Uptake ◽  
Male Athletes ◽  
Model Combining ◽  
Hockey Players ◽  
Explained Variance ◽  
Total Body ◽  
Size Descriptor

Peak oxygen uptake (V̇O2peak) is routinely expressed in litres per minute and by unit of body mass (mL·kg−1·min−1) despite the theoretical and statistical limitations of using ratios. Allometric modeling is an effective approach for partitioning body-size effects in a performance variable. The current study examined the relationships among chronological age (CA), skeletal age (SA), total body and appendicular size descriptors, and V̇O2peakin male adolescent roller hockey players. Seventy-three Portuguese, highly trained male athletes (CA, 15.4 ± 0.6 years; SA, 16.4 ± 1.5 years; stature, 169.9 ± 6.9 cm; body mass, 63.7 ± 10.7 kg; thigh volume, 4.8 ± 1.0 L) performed an incremental maximal test on a motorized treadmill. Exponents for body size descriptors were 2.15 for stature (R2= 0.30, p < 0.01) and 0.55 for thigh volume (R2= 0.46, p < 0.01). The combination of stature or thigh volume and CA or SA, and CA2or SA2, increased the explained variance in V̇O2peak(R2ranged from 0.30 to 0.55). The findings of the allometric model combining more than 1 body size descriptor (i.e., stature and thigh volume) in addition to SA and CA2were not significant. Results suggest that thigh volume and SA are the main contributors to interindividual variability in aerobic fitness.

Maturity Status Does Not Exert Effects on Aerobic Fitness in Soccer Players After Appropriate Normalization for Body Size

2016 ◽  
Vol 28 (3) ◽  
pp. 456-465 ◽  
Author(s):  
Giovani Dos Santos Cunha ◽  
Marco Aurélio Vaz ◽  
Jeam Marcel Geremia ◽  
Gabriela T. Leites ◽  
Rafael Reimann Baptista ◽  
...  
Keyword(s):  
Body Size ◽  
Aerobic Fitness ◽  
Ventilatory Threshold ◽  
Peak Oxygen Uptake ◽  
Muscle Volume ◽  
Soccer Players ◽  
Chronological Age ◽  
Maximal Exercise Test ◽  
Positive Effect ◽  
Size Descriptor

The present study investigated the effects of pubertal status on peak oxygen uptake (VO2peak), respiratory compensation point (RCP), and ventilatory threshold (VT) in young soccer players using different body size descriptors. Seventy-nine soccer players (14 prepubescent, 38 pubescent and 27 postpubescent) participated in this study. A maximal exercise test was performed to determine the VO2peak, RCP, and VT. Ultrasonography was used to measure lower limb muscle volume (LLMV). LLMV (mL-b) was rated as the most effective body size descriptor to normalize VO2peak (mLO2•mL-0.43•min-1), RCP (mLO2•mL-0.48•min-1), and VT (mLO2•mL-0.40•min-1). The values of VO2peak, RCP, and VT relative to allometric exponents derived by LLMV were similar among groups (p > .05; 0.025 < η2 < 0.059) when the effect of chronological age was controlled. Allometric VO2peak, RCP, and VT values were: 100.1 ± 7.9, 107.5 ± 9.6, and 108.0 ± 10.3 mLO2.mL-0.43•min-1; 51.8 ± 5.3, 54.8 ± 4.7, and 57.3 ± 5.8 mLO2•mL-0.48•min-1; and 75.7 ± 7.1, 79.4 ± 7.0, and 80.9 ± 8.3 mLO2•mL-0.40•min-1 for prepubertal, pubertal, and postpubertal groups, respectively. Maturity status showed no positive effect on VO2peak, RCP, and VT when the data were properly normalized by LLMV in young soccer players. Allometric normalization using muscle volume as a body size descriptor should be used to compare aerobic fitness between soccer players heterogeneous in chronological age, maturity status, and body size.

The stress response in human peripheral mononuclear cells is related to aerobic fitness and Body Mass Index

2019 ◽  
Vol 178 (6) ◽  
Author(s):  
Kelsey C. Bourbeau ◽  
Mattina M. Rosinski ◽  
Taylor M. Szczygiel ◽  
Ryan Pettit-Mee ◽  
Jenna E. Sessions ◽  
...  
Keyword(s):  
Body Mass Index ◽  
Stress Response ◽  
Body Mass ◽  
Aerobic Fitness ◽  
Mononuclear Cells ◽  
Peripheral Mononuclear Cells

scholarly journals Morphological determinants of jumping performance in the Iberian green frog

2019 ◽  
Vol 66 (4) ◽  
pp. 417-424
Author(s):  
Gregorio Moreno-Rueda ◽  
Abelardo Requena-Blanco ◽  
Francisco J Zamora-Camacho ◽  
Mar Comas ◽  
Guillem Pascual
Keyword(s):  
Body Size ◽  
Body Mass ◽  
Fluctuating Asymmetry ◽  
Hind Limb ◽  
Limb Length ◽  
Age Classes ◽  
Jumping Performance ◽  
Hind Limbs ◽  
Selective Forces ◽  
Pelophylax Perezi

Abstract Predation is one of the main selective forces in nature, frequently selecting potential prey for developing escape strategies. Escape ability is typically influenced by several morphological parameters, such as morphology of the locomotor appendices, muscular capacity, body mass, or fluctuating asymmetry, and may differ between sexes and age classes. In this study, we tested the relationship among these variables and jumping performance in 712 Iberian green frogs Pelophylax perezi from an urban population. The results suggest that the main determinant of jumping capacity was body size (explaining 48% of variance). Larger frogs jumped farther, but jumping performance reached an asymptote for the largest frogs. Once controlled by structural body size, the heaviest frogs jumped shorter distances, suggesting a trade-off between fat storage and jumping performance. Relative hind limb length also determined a small but significant percentage of variance (2.4%) in jumping performance—that is, the longer the hind limbs, the greater the jumping capacity. Juveniles had relatively shorter and less muscular hind limbs than adults (for a given body size), and their jumping performance was poorer. In our study population, the hind limbs of the frogs were very symmetrical, and we found no effect of fluctuating asymmetry on jumping performance. Therefore, our study provides evidence that jumping performance in frogs is not only affected by body size, but also by body mass and hind limb length, and differ between age classes.

scholarly journals Ontogeny of body size and shape of Antarctic and subantarctic fur seals

2007 ◽  
Vol 85 (12) ◽  
pp. 1275-1285 ◽  
Author(s):  
Sebastián P. Luque ◽  
Edward H. Miller ◽  
John P.Y. Arnould ◽  
Magaly Chambellant ◽  
Christophe Guinet
Keyword(s):  
Body Size ◽  
Body Mass ◽  
Morphological Traits ◽  
Body Shape ◽  
Size And Shape ◽  
Fur Seals ◽  
Fur Seal ◽  
Adult Body ◽  
Weaning Age ◽  
Lactation Duration

Pre- and post-weaning functional demands on body size and shape of mammals are often in conflict, especially in species where weaning involves a change of habitat. Compared with long lactations, brief lactations are expected to be associated with fast rates of development and attainment of adult traits. We describe allometry and growth for several morphological traits in two closely related fur seal species with large differences in lactation duration at a sympatric site. Longitudinal data were collected from Antarctic ( Arctocephalus gazella (Peters, 1875); 120 d lactation) and subantarctic ( Arctocephalus tropicalis (Gray, 1872); 300 d lactation) fur seals. Body mass was similar in neonates of both species, but A. gazella neonates were longer, less voluminous, and had larger foreflippers. The species were similar in rate of preweaning growth in body mass, but growth rates of linear variables were faster for A. gazella pups. Consequently, neonatal differences in body shape increased over lactation, and A. gazella pups approached adult body shape faster than did A. tropicalis pups. Our results indicate that preweaning growth is associated with significant changes in body shape, involving the acquisition of a longer, more slender body with larger foreflippers in A. gazella. These differences suggest that A. gazella pups are physically more mature at approximately 100 d of age (close to weaning age) than A. tropicalis pups of the same age.

scholarly journals Intraspecific Variation in Maximum Ingested Food Size and Body Mass in Varecia rubra and Propithecus coquereli

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Adam Hartstone-Rose ◽  
Jonathan M. G. Perry
Keyword(s):  
Body Size ◽  
Body Mass ◽  
Individual Variation ◽  
Size Variation ◽  
Maximum Size ◽  
Least Squares Regression ◽  
Scaling Relationship ◽  
Varecia Rubra ◽  
Food Size ◽  
The Relationship

In a recent study, we quantified the scaling of ingested food size (Vb )—the maximum size at which an animal consistently ingests food whole—and found that Vb scaled isometrically between species of captive strepsirrhines. The current study examines the relationship between Vb and body size within species with a focus on the frugivorous Varecia rubra and the folivorous Propithecus coquereli. We found no overlap in Vb between the species (all V. rubra ingested larger pieces of food relative to those eaten by P. coquereli), and least-squares regression of Vb and three different measures of body mass showed no scaling relationship within each species. We believe that this lack of relationship results from the relatively narrow intraspecific body size variation and seemingly patternless individual variation in Vb within species and take this study as further evidence that general scaling questions are best examined interspecifically rather than intraspecifically.

Speed, stride frequency and energy cost per stride: how do they change with body size and gait?

1988 ◽  
Vol 138 (1) ◽  
pp. 301-318 ◽  
Author(s):  
N. C. Heglund ◽  
C. R. Taylor
Keyword(s):  
Body Size ◽  
Body Mass ◽  
Energy Cost ◽  
Reaction Force ◽  
Stride Frequency ◽  
Energetic Cost ◽  
Published Data ◽  
Frequency Change ◽  
Cost Of Locomotion ◽  
The Cost

In this study we investigate how speed and stride frequency change with body size. We use this information to define ‘equivalent speeds’ for animals of different size and to explore the factors underlying the six-fold difference in mass-specific energy cost of locomotion between mouse- and horse-sized animals at these speeds. Speeds and stride frequencies within a trot and a gallop were measured on a treadmill in 16 species of wild and domestic quadrupeds, ranging in body size from 30 g mice to 200 kg horses. We found that the minimum, preferred and maximum sustained speeds within a trot and a gallop all change in the same rather dramatic manner with body size, differing by nine-fold between mice and horses (i.e. all three speeds scale with about the 0.2 power of body mass). Although the absolute speeds differ greatly, the maximum sustainable speed was about 2.6-fold greater than the minimum within a trot, and 2.1-fold greater within a gallop. The frequencies used to sustain the equivalent speeds (with the exception of the minimum trotting speed) scale with about the same factor, the −0.15 power of body mass. Combining this speed and frequency data with previously published data on the energetic cost of locomotion, we find that the mass-specific energetic cost of locomotion is almost directly proportional to the stride frequency used to sustain a constant speed at all the equivalent speeds within a trot and a gallop, except for the minimum trotting speed (where it changes by a factor of two over the size range of animals studied). Thus the energy cost per kilogram per stride at five of the six equivalent speeds is about the same for all animals, independent of body size, but increases with speed: 5.0 J kg-1 stride-1 at the preferred trotting speed; 5.3 J kg-1 stride-1 at the trot-gallop transition speed; 7.5 J kg-1 stride-1 at the preferred galloping speed; and 9.4 J kg-1 stride-1 at the maximum sustained galloping speed. The cost of locomotion is determined primarily by the cost of activating muscles and of generating a unit of force for a unit of time. Our data show that both these costs increase directly with the stride frequency used at equivalent speeds by different-sized animals. The increase in cost per stride with muscles (necessitating higher muscle forces for the same ground reaction force) as stride length increases both in the trot and in the gallop.

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