Evidence of morphological adaptation to life underwater: Sternal keel affects swimming speed in giant water scavenger beetles (Coleoptera: Hydrophilidae: Hydrophilini)

2021 ◽  
Author(s):  
Ryosuke Matsushima
Keyword(s):  
Body Size ◽  
Gas Exchange ◽  
Body Mass ◽  
Swimming Speed ◽  
Aquatic Insects ◽  
Morphological Traits ◽  
Aquatic Environments ◽  
Morphological Adaptation ◽  
Ecological Traits ◽  
Oscillatory Movement

Fundamentally, insects evolved on land and secondarily inhabited aquatic environments multiple times. To live underwater, aquatic insects have acquired enormously variable morphological, developmental, physiological, and ecological traits, such as gas exchange systems and swimming-related characteristics. Giant water scavenger beetles of the tribe Hydrophilini (Coleoptera: Hydrophilidae) are characterized by the presence of sternal keel, which often extends posteriorly. Despite being a conspicuous morphological trait, its function remains unclear. Here, I verified two hypotheses: keel affects (1) submergence time following air replacement as well as (2) speed and oscillatory movement during forward swimming in Hydrophilus acuminatus Motschulsky, 1854. Submergence time was affected by body mass rather than keel removal; in other words, larger individuals replaced their gas gills more frequently. Keel removal reduced swimming speed by 12.5%. These observations support hypothesis (2) and are also consistent with previous speculations that sternal keel is a key adaptation to swim, but the results showed that the degree of oscillation was closely related to body mass but not keel removal. Further studies are warranted to elucidate precise factors through which the presence of keel increases swimming speed. Such studies would provide clues into understanding the associations amongst body size, swimming methods, and morphological traits.

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 Overcoming Drag at the Water-Air Interface Constrains Body Size in Whirligig Beetles

Fluids ◽  
2021 ◽  
Vol 6 (7) ◽  
pp. 249
Author(s):  
Ludovic Jami ◽  
Grey T. Gustafson ◽  
Thomas Steinmann ◽  
Miguel Piñeirua ◽  
Jérôme Casas
Keyword(s):  
Body Size ◽  
Swimming Speed ◽  
Minimal Model ◽  
Aquatic Insects ◽  
Size Range ◽  
Optimal Size ◽  
Air Interface ◽  
Evolutionary Trajectories

Whirligig beetles (Coleoptera: Gyrinidae) are among the best swimmers of all aquatic insects. They live mostly at the water’s surface and their capacity to swim fast is key to their survival. We present a minimal model for the viscous and wave drags they face at the water’s surface and compare them to their thrust capacity. The swimming speed accessible is thus derived according to size. An optimal size range for swimming at the water’s surface is observed. These results are in line with the evolutionary trajectories of gyrinids which evolved into lineages whose members are a few milimeter’s long to those with larger-sized genera being tens of millimeters in length. The size of these beetles appears strongly constrained by the fluid mechanical laws ruling locomotion and adaptation to the water-air interface.

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 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.

Growth of Southern Elephant Seals, Mirounga leonina, during their First Foraging Trip

1997 ◽  
Vol 45 (5) ◽  
pp. 447 ◽  
Author(s):  
Cameron M. Bell ◽  
Harry R. Burton ◽  
Mark A. Hindell
Keyword(s):  
Body Composition ◽  
Body Size ◽  
Body Mass ◽  
First Year ◽  
Mirounga Angustirostris ◽  
Mirounga Leonina ◽  
Elephant Seals ◽  
Southern Elephant Seals ◽  
First Year Of Life ◽  
Foraging Skills

A longitudinal study of growth of southern elephant seals, Mirounga leonina, during their first foraging trip was undertaken at Macquarie Island. On average, body mass increased by 75% while foraging at sea, with individuals growing at 0.34 ± 0.12 (s.d.) kg day-1 (n = 64), and spending 182 ± 51 days (n = 64) at sea. Relatively smaller changes in body length were recorded during the same period, suggesting that growth was composed primarily of adjustments to body composition, rather than increases in gross body size. This may be in response to the functional demands of pelagic life. Body size established early in life (birth mass and departure mass) positively influenced body mass upon return from the first foraging trip. Growth rate, however, was negatively related to departure mass for females, and this is hypothesised to be related to sex differences in body composition, as well as intrasex differences in foraging skills, diving ability and food- conversion efficiency. Despite this, there was no detectable age-specific sexual dimorphism in the first year of life. Animals that were at sea longer tended to return in better body condition. Interspecific comparison suggests that southern elephant seals grow more than do northern elephant seals, Mirounga angustirostris, and this difference may be related to prey abundance and distribution.

The demography of limb dominance, body-mass index, and metatarsus adductus deformity

1998 ◽  
Vol 88 (9) ◽  
pp. 429-436 ◽  
Author(s):  
JR Montague ◽  
M Bovarnick ◽  
SC Effren ◽  
CC Southerland
Keyword(s):  
Body Mass Index ◽  
Body Size ◽  
Body Mass ◽  
South Florida ◽  
X Rays ◽  
Statistical Association ◽  
Metatarsus Adductus ◽  
Average Body Mass ◽  
Average Body ◽  
Limb Dominance

To test the null hypothesis that limb dominance (laterality) and side of complaint are not associated in a diverse population, nearly 400 patients (40% male, 60% female) of varying age and body size from three South Florida podiatric medical teaching facilities were surveyed in 1995-1996. Radiographs of feet were available for 15% of the patients, and the metatarsus adductus angle was measured on each x-ray. The typical patient was a women (median age, 49 years) of average body weight and average body-mass index. No statistical association was found between laterality and side of complaint in the broader sample, although a significant association did appear in the subsample of patients with bilateral x-rays. The prevalence of metatarsus adductus deformity (metatarsus adductus angle > 15 degrees) among patients with x-rays was 62%. No sex-specific, age-specific, or body size-specific associations were found between handedness and metatarsus adductus deformity.

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