Inter- and intraspecific vigilance patterns of two sympatric Tibetan ungulates

2019 ◽  
Vol 101 (2) ◽  
pp. 498-506 ◽  
Author(s):  
Yunchao Luo ◽  
Lin Wang ◽  
Le Yang ◽  
Xinxin Wang ◽  
Ming Tan ◽  
...  
Keyword(s):  
Body Size ◽  
Body Mass ◽  
Group Size ◽  
Sexually Dimorphic ◽  
Small Animals ◽  
Wild Ungulates ◽  
Small Female ◽  
Social Monitoring ◽  
Negative Effect ◽  
Large Groups

Abstract Vigilance is an important antipredation technique that can be affected by many factors, such as body size and group size. Small animals are more vulnerable than large ones, so the former are expected to behave more vigilantly than the latter. This effect of body size on vigilance may occur inter- or intraspecifically. We studied the vigilance behavior of two sympatric wild ungulates, Tibetan antelopes (Pantholops hodgsonii) and Tibetan gazelles (Procapra picticaudata). Tibetan antelopes, with a body size of 33 kg are much larger than Tibetan gazelles, with a body size of approximately 14 kg. Tibetan antelopes are sexually and body-size dimorphic; that is, males are much heavier than females. Alternately, Tibetan gazelles are sexually dimorphic but the sexes do not differ in weight. Tibetan gazelles scanned their environment more frequently than Tibetan antelopes did. Small female Tibetan antelopes scanned their environment more frequently than males did, whereas male Tibetan gazelles scanned their environment more frequently than females did. Group size did not affect the vigilance of Tibetan gazelle, but its negative effect on the vigilance of male Tibetan antelopes was marginally significant. In female Tibetan antelopes, vigilance in large groups was high probably because of scramble competition and social monitoring. Our results suggested that body mass and group size play an important role in shaping the vigilance of these two rare Tibetan ungulates.

scholarly journals Does Group Size Affect Field Metabolic Rate of Arabian Babbler (Turdoides squamiceps) Nestlings?

The Auk ◽  
2001 ◽  
Vol 118 (2) ◽  
pp. 525-528
Author(s):  
Avner Anava ◽  
Michael Kam ◽  
Amiram Shkolnik ◽  
A. Allan Degen
Keyword(s):  
Metabolic Rate ◽  
Group Size ◽  
Annual Number ◽  
Field Metabolic Rate ◽  
Negative Effect ◽  
Group Feeding ◽  
Group Members ◽  
Single Nest ◽  
Large Groups ◽  
Arabian Babbler

Abstract Arabian Babblers (Turdoides squamiceps) are territorial, cooperative breeding passerines in which groups consist of parents and helpers. All members of the group feed nestlings in a single nest and all group members provision at similar rates. We hypothesized that the field metabolic rate (FMR) of Arabian Babbler nestlings is related to group feeding; that is, FMR would be greater in nestlings of larger rather than smaller sized groups. To test that hypothesis, we measured FMR of 10 day old nestlings from small (2 and 3 individuals), medium (4 and 5 individuals), and large (6 or more individuals) groups. We also determined number of hatchlings and fledglings produced per group. There was an increase in body mass and FMR from small to medium-sized groups, but there was a levelling off or decrease in those parameters in large groups. That suggests that there is an optimum group number for provisioning nestlings, above which there may be a negative effect. The relationship between group size and annual number of eggs was not significant, but there was a positive and linear relationship between group size and annual fledglings production. Thus, more eggs reached the fledgling stage with an increase in group size, suggesting that larger groups are better able to defend the nest against predators.

Group composition and cohesion in sympatric white-tailed deer and mule deer

2003 ◽  
Vol 81 (7) ◽  
pp. 1119-1130 ◽  
Author(s):  
Susan Lingle
Keyword(s):  
Group Size ◽  
Mule Deer ◽  
Size Composition ◽  
Odocoileus Hemionus ◽  
Habitat Conditions ◽  
Small Female ◽  
Habitat Variation ◽  
The Social ◽  
Southern Alberta ◽  
Large Groups

White-tailed deer (Odocoileus virginianus) have been reported to live in smaller groups than mule deer (Odocoileus hemionus). Group size, however, generally varies with habitat conditions, and no comparison has been made between the social structures of the two species living in the same ecological conditions. I compared the size, composition, and stability of groups formed by sympatric whitetails and mule deer living in a prairie habitat in southern Alberta. Seasonal trends were similar for the two species. Females and fawns usually formed small groups during summer. Larger mixed-sex groups became increasingly common during winter, well after the breeding season. Despite the similar seasonal trend, mule deer were significantly more likely than whitetails to occur in relatively large groups composed of both sexes during winter, and whitetails were more likely to occur in small female groups. Mule deer groups were more stable than whitetail groups, and marked mule deer fawns developed strong associations with other known fawns. Habitat variation was limited and was not related to group size. These results show that the composition and cohesion of whitetail and mule deer groups differ, even when the species live in similar circumstances. The differences in grouping behaviour, larger more cohesive groups formed by mule deer than by whitetails, are consistent with those expected to result from the selection pressure of predation.

Sexual segregation in bison: a test of multiple hypotheses

Behaviour ◽  
2005 ◽  
Vol 142 (7) ◽  
pp. 897-927 ◽  
Author(s):  
Eric W. Schaad ◽  
David S. Wiseman ◽  
Royce R. Huber ◽  
Michael S. Mooring ◽  
Dominic D. Reisig ◽  
...  
Keyword(s):  
Body Size ◽  
Predation Risk ◽  
Sexual Segregation ◽  
Bison Bison ◽  
Sexually Dimorphic ◽  
Activity Budgets ◽  
Single Sex ◽  
Multiple Hypotheses ◽  
Mixed Groups ◽  
Large Groups

AbstractSexual segregation, in which males and females form separate groups for most of the year, is common in sexually dimorphic ungulates. We tested multiple hypotheses to explain sexual segregation in bison (Bison bison) at National Bison Range, Montana and Fort Niobrara National Wildlife Refuge, Nebraska during June-August of 2002-2003. Fieldwork involved use of GPS to record space use by segregated groups, vegetation transects to measure forage availability, fecal analyses to document diet composition and quality, and behavioural observations to characterize activity budgets. During sexual segregation, males in bull groups used areas with greater per capita abundance of forage, higher proportion of weeds, and less nutritious grasses (as indicated by lower % fecal nitrogen) compared with females in cow or mixed groups. However, there was no difference between the sexes in activity budgets, predation risk factors, or distance to water. Single-sex bull groups were no more synchronized in activity than mixed groups. These results support the 'sexual dimorphism-body size hypothesis', which proposes that males segregate from females because their larger body size requires more abundant forage, while longer ruminal retention permits efficient use of lower-quality forage. The gastrocentric model, based on the digestive physiology and foraging requirements of dimorphic ungulates, supplies the most likely proximate mechanism for bison sexual segregation. Our results would also partly support the 'reproductive strategy-predation risk hypothesis' if females form large groups to reduce predation risk. The predictions of the 'activity budget hypothesis' were not supported for bison.

scholarly journals Limitations on Animal Flight Performance

1991 ◽  
Vol 160 (1) ◽  
pp. 71-91 ◽  
Author(s):  
C. P. ELLINGTON
Keyword(s):  
Body Size ◽  
Body Mass ◽  
Specific Power ◽  
Small Animals ◽  
Flight Performance ◽  
Wide Range ◽  
Speed Range ◽  
Speed Performance ◽  
Flight Muscles ◽  
Animal Flight

Flight performance seems to change systematically with body size: small animals can hover and fly over a wide range of speeds, but large birds taxi for takeoff and then fly over a narrow speed range. The traditional explanation for this is that the mass-specific power required for flight varies with speed according to a U-shaped curve, and it also scales between m0 and m1/6, where m is body mass. The mass-specific power available from the flight muscles is assumed to scale as m−1/3. As available power decreases with increasing body size, the range of attainable flight speeds becomes progressively reduced until the largest animals can only fly in the trough of the U-shaped curve. Above a particular size, the available power is insufficient and flapping flight is not possible. The underlying assumptions of this argument are examined in this review. Metabolic measurements are more consistent with a J-shaped curve, with little change in power from hovering to intermediate flight speeds, than with a U-shaped curve. Scaling of the mass-specific power required to fly agrees with predictions. The mass-specific power available from, the muscles, estimated from maximal loading studies, varies as m0.13. This scaling cannot be distinguished from that of the power required to fly, refuting the argument that power imposes an intrinsic scaling on flight performance. It is suggested instead that limitations on low-speed performance result from an adverse scaling of lift production with increasing body size.

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.

Theoretical and empirical scaling patterns and topological homology in bone trabeculae.

1998 ◽  
Vol 201 (4) ◽  
pp. 573-590
Author(s):  
S M Swartz ◽  
A Parker ◽  
C Huo
Keyword(s):  
Body Size ◽  
Surface Area ◽  
Cancellous Bone ◽  
Structural Design ◽  
Theoretical Models ◽  
Small Animals ◽  
Bone Trabeculae ◽  
Large Animals ◽  
Vertebrate Skeleton ◽  
Area And Volume

Trabecular or cancellous bone is a major element in the structural design of the vertebrate skeleton, but has received little attention from the perspective of the biology of scale. In this study, we investigated scaling patterns in the discrete bony elements of cancellous bone. First, we constructed two theoretical models, representative of the two extremes of realistic patterns of trabecular size changes associated with body size changes. In one, constant trabecular size (CTS), increases in cancellous bone volume with size arise through the addition of new elements of constant size. In the other model, constant trabecular geometry (CTG), the size of trabeculae increases isometrically. These models produce fundamentally different patterns of surface area and volume scaling. We then compared the models with empirical observations of scaling of trabecular dimensions in mammals ranging in mass from 4 to 40x10(6)g. Trabecular size showed little dependence on body size, approaching one of our theoretical models (CTS). This result suggests that some elements of trabecular architecture may be driven by the requirements of maintaining adequate surface area for calcium homeostasis. Additionally, we found two key consequences of this strongly negative allometry. First, the connectivity among trabecular elements is qualitatively different for small versus large animals; trabeculae connect primarily to cortical bone in very small animals and primarily to other trabeculae in larger animals. Second, small animals have very few trabeculae and, as a consequence, we were able to identify particular elements with a consistent position across individuals and, for some elements, across species. Finally, in order to infer the possible influence of gross differences in mechanical loading on trabecular size, we sampled trabecular dimensions extensively within Chiroptera and compared their trabecular dimensions with those of non-volant mammals. We found no systematic differences in trabecular size or scaling patterns related to locomotor mode.

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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