Desiccation resistance in arboreal and terrestrial ants

ABSTRACT Arboreal and terrestrial ants were exposed to 0, 25, 50, 75 and 100 (control)% r.h., at 30^oC. Desiccation resistance increased with body size (as dry weight^0.55), but not as quickly as expected from the consequences of the surface area and volume relationship (as dry weight^0.67). Arboreal ants took 8 times longer to die than terrestrial ants of comparable size. Even after size effects were removed, desiccation resistance differed between various terrestrial species and showed a correlation with foraging patterns.
Arboreal and terrestrial ants whose waterproofing epicuticular lipids were removed by chloroform: methanol extraction had equally high water loss rates at 0% r.h. Unextracted arboreal ants had water loss rates half those of unextracted terrestrial ants, suggesting that differences between them were based on differences in epicuticular lipids. The lower water loss rates of arboreal ants contributed significantly to their longer survival under desiccation. Arboreal ants also had greater total rectal pad area than terrestrial ants, suggesting that they may be able to reclaim faecal water more effectively. There were no differences in the minimum viable water content between the two groups of ants. Both had water loss tolerances comparable with those of arthropods adapted to xeric environments. Initial water loss rates could not account for all of the differences in desiccation resistance between arboreal and terrestrial ants. Other adaptations to desiccation stress by arboreal ants are likely.
Comparisons of water loss rates and desiccation resistance between arboreal and desert ants suggest that the arboreal habitat is at least as stressful as the desert habitat.     

Scaling of the limb long bones to body mass in terrestrial mammals

Long‐bone scaling has been analyzed in a large number of terrestrial mammals for which body masses were known. Earlier proposals that geometric or elastic similarity are suitable as explanations for long‐bone scaling across a large size range are not supported. Differential scaling is present, and large mammals on average scale with lower regression slopes than small mammals. Large mammals tend to reduce bending stress during locomotion by having shorter limb bones than predicted rather than by having very thick diaphyses, as is usually assumed. The choice of regression model used to describe data samples in analyses of scaling becomes increasingly important as correlation coefficients decrease, and theoretical models supported by one analysis may not be supported when applying another statistical model to the same data. Differences in limb posture and locomotor performance have profound influence on the amount of stress set up in the appendicular bones during rigorous physical activity and make it unlikely that scaling of long bones across a large size range of terrestrial mammals can be satisfactorily explained by any one power function. J. Morphol. 239:167–190, 1999. © 1999 Wiley‐Liss, Inc.     

Structural adaptations of the femur and humerus to arboreal and terrestrial environments in three species of macaque

One reason to measure cross-sectional structural properties of primate long bones is to define mechanically relevant complexes of traits that describe the adaptation of bone to different biomechanical environments. This can be effectively accomplished when congeneric species having different postural and locomotor behaviors are compared. This paper compares the cross-sectional geometry of the femur and humerus in three behaviorally different macaque species as a basis for defining such patterns. Cross-sectional moments of inertia in the standard anatomical planes were calculated at five locations along the diaphyses of the femur and humerus in Macaca fascicularis, M. nemestrina, and M. mulatta. The data suggest that the "barrel-shaped" femur is associated with behaviors for which long limbs and small body size are an asset. This may be associated with, but is not restricted to, leaping behaviors. The data also suggest that structural rigidity of the femur and humerus is greater per unit body weight in primates that spend significant amounts of time in terrestrial environments than in those that are more restricted to climbing in arboreal environments.     

Influences of limb proportions and body size on locomotor kinematics in terrestrial primates and fossil hominins

During locomotion, mammalian limb postures are influenced by many factors including the animal's limb length and body mass. Polk (2002) compared the gait of similar-sized cercopithecine monkeys that differed limb proportions and found that longer-limbed monkeys usually adopt more extended joint postures than shorter-limbed monkeys in order to moderate their joint moments. Studies of primates as well as non-primate mammals that vary in body mass have demonstrated that larger animals use more extended limb postures than smaller animals. Such extended postures in larger animals increase the extensor muscle mechanical advantage and allow postures to be maintained with relatively less muscular effort (Polk, 2002; Biewener 1989). The results of these previous studies are used here to address two anthropological questions. The first concerns the postural effects of body mass and limb proportion differences between australopithecines and members of the genus Homo. That is, H. erectus and later hominins all have larger body mass and longer legs than australopithecines, and these anatomical differences suggest that Homo probably used more extended postures and probably required relatively less muscular force to resist gravity than the smaller and shorter-limbed australopithecines. The second question investigates how animals with similar size but different limb proportions differ in locomotor performance. The effects of limb proportions on gait are relevant to inferring postural and locomotor differences between Neanderthals and modern Homo sapiens which differ in their crural indices and relative limb length. This study demonstrates that primates with relatively long limbs achieve higher walking speeds while using lower stride frequencies and lower angular excursions than shorter-limbed monkeys, and these kinematic differences may allow longer-limbed taxa to locomote more efficiently than shorter-limbed species of similar mass. Such differences may also have characterized the gait of Homo sapiens in comparison to Neanderthals, but more experimental data on humans that vary in limb proportions are necessary in order to evaluate this question more thoroughly.     

Brief communication: Forelimb compliance in arboreal and terrestrial opossums

Primates display high forelimb compliance (increased elbow joint yield) compared to most other mammals. Forelimb compliance, which is especially marked among arboreal primates, moderates vertical oscillations of the body and peak vertical forces and may represent a basal adaptation of primates for locomotion on thin, flexible branches. However, Larney and Larson (Am J Phys Anthropol 125 [2004] 42–50) reported that marsupials have forelimb compliance comparable to or greater than that of most primates, but did not distinguish between arboreal and terrestrial marsupials. If forelimb compliance is functionally linked to locomotion on thin branches, then elbow yield should be highest in marsupials relying on arboreal substrates more often. To test this hypothesis, we compared forelimb compliance between two didelphid marsupials, Caluromys philander (an arboreal opossum relying heavily on thin branches) and Monodelphis domestica (an opossum that spends most of its time on the ground). Animals were videorecorded while walking on a runway or a horizontal 7‐mm pole. Caluromys showed higher elbow yield (greater changes in degrees of elbow flexion) on both substrates, similar to that reported for arboreal primates. Monodelphis was characterized by lower elbow yield that was intermediate between the values reported by Larney and Larson (Am J Phys Anthropol 125 [2004] 42–50) for more terrestrial primates and rodents. This finding adds evidence to a model suggesting a functional link between arboreality—particularly locomotion on thin, flexible branches—and forelimb compliance. These data add another convergent trait between arboreal primates, Caluromys, and other arboreal marsupials and support the argument that all primates evolved from a common ancestor that was a fine‐branch arborealist. Am J Phys Anthropol, 2010. © 2009 Wiley‐Liss, Inc.     

Primate visual signals in noisy environments

Most animals and plants need to send signals and rely on some sort of response. For an active receptor of signals, virtually all the signal transmissions that litter the environment, bar those that are functional at any given moment, can be described as 'noise'. I concentrate here on some primate examples where loud calls combine with 'loud' colouring and patterns, to suggest that increasing the intensity of signals can help overcome the problem of 'noise'. I also present evidence that certain ecological conditions favour use of the visual channel. I use some examples, drawn from African guenons, to suggest that visual patterns broadcast on this channel have evolved and have, effectively, been elaborated to conform with certain optical principles. These optical properties minimize ambiguity and enhance species-specific (or at least population-specific) distinctiveness. The abilities of ancestral forest primates to discriminate between functional signals and visual 'noise' may have played an important part in providing the basis for our own hominin ancestors' visual proficiencies.     

Gait mechanics of lemurid primates on terrestrial and arboreal substrates

Aspects of gait mechanics of two lemurid species were explored experimentally. Substrate reaction forces were recorded for three animals each of L. catta and E. fulvus walking and running at voluntary speeds either on a wooden runway with an integrated force platform or on elevated pole supports with a section attached to the force platform. The average height of the back over these substrates and fluctuations in this height were evaluated using video-analysis. Animals preferred walking gaits and lower speeds on the poles, and gallops and higher speeds on the ground. At overlapping speeds, few adjustments to substrate types were identified. Hind limb peak forces are usually lower on the poles than on the ground, and the caudal back is closer to the substrate. This suggests that greater hind limb flexion and reduced limb stiffness occurred on the poles. The support phases for both limbs at higher speeds are slightly elongated on the poles. Forelimb peak forces are not lower, and the trajectory of the caudal back does not follow a smoother path, i.e., not all elements of a compliant gait are present on the simulated arboreal substrates. The horizontal, rigid poles, offered as substitutes for branchlike supports in the natural habitat, may not pose enough of a challenge to require more substantial gait adjustments. Across substrates, forelimb peak forces are generally lower than hind limb peak forces. The interlimb force distribution is similar to that of most other primates with more even limb lengths. Walking gaits present a greater divergence in fore- and hind limb forces than galloping gaits, which are associated with higher forces. The more arboreal E. fulvus has higher forelimb forces than the more terrestrial L. catta, unlike some anthropoid species in which the arborealists have lower forelimb forces than the terrestrialists. As in other primate and nonprimate quadrupeds, the major propulsive thrust comes from the hind limbs in both lemurs. While our data confirm certain aspects of primate gait mechanics (e.g., generally higher hind limb forces), they do not fully support the notion of greater limb compliance. Neither a compliant forelimb on branchlike supports, nor a negative correlation of forelimb force magnitudes with degree of arboreality were observed. Increasing forelimb-to-hind-limb-force-ratios with increasing speed and force magnitudes are also not expected under this paradigm.     

The jump as a fast mode of locomotion in arboreal and terrestrial biotopes

The jump is always used for locomotion. For its execution in arboreal and terrestrial biotopes the requirements are of somewhat different nature. In an arboreal biotope the jump is characterized by a rapid progression through discontinuous substrates and the ability to take off from a small area and a secure landing on a spot. This requires well coordinated movements in all phases of the jump. On the ground, the jump is less frequent and often used for crossing obstacles or gaps. In primates both variants can be observed. In order to relate the details of locomotor behaviour to a certain environment, the biomechanics of jumping are analyzed in five primate species: The three mainly arboreal prosimian species Galago moholi, the smallest and most specialized leaper of all, Galago garnettii, a medium-sized bushbaby with some capacities for jumping, and Lemur catta also with some abilities to jump. The two simian species, Macaca fuscata and Homo sapiens, are usually terrestrial and have good jumping capacities, although not in terms of quantity. The investigation is based on high-speed motion analyses (100-500 frames/second) and the synchronized records of a force-plate from which all subjects had to jump off. On the basis of the results two kinds of jumping can be distinguished: standing and running jumps. The three prosimian species perform standing jumps. Dorsiflexion of their tails compensates ventrally oriented rotational moments of the trunk during body extension at take-off. The upward arm swing yields an overall increase in take-off velocity without additional muscular force exerted by the legs. The main difference among the species are the high relative forces in the small Galago moholi (up to 13 times body weight) as compared to the larger G. garnettii (8.5 times body weight) and the even larger Lemur catta (4.5 times body weight). In Homo sapiens the standing jump is characterized by an extensive arm swing backward, which is then followed by a forward and upward movement. The velocity at take-off is much smaller if compared to the prosimians. The running jump in Macaca fuscata is always preceded by at least one gallop cycle. The body assumes a ball shape at the beginning of the actual take-off. This is advantageous for rotating the body into a position in which the trunk axis is in line with the direction of movement. The tail of the Japanese macaque is too short to compensate the trunk's lift exerted on the hip region by the extending hindlimbs.(ABSTRACT TRUNCATED AT 400 WORDS)     

Sexual differences in Neanderthal limb bones

European and Near Eastern Neanderthal postcranial remains have been analyzed to determine the degrees of sexual dimorphism in limb bone size and robusticity present among the Neanderthals. The remains were sexed on the basis of pelvic morphology where possible (seven males and three females) and otherwise on the basis of absolute size employing limb bone lengths and articular dimensions (12 males and 15 females). Neanderthal sexual size dimorphism, both within single site samples and in the total sexable sample, is virtually the same as that of recent human samples. Furthermore, despite a tendency towards more robust limbs, the Neanderthals exhibit sexual dimorphism in limb bone shaft and articular robusticity similar to that of recent human samples. By the time of the Neanderthals, sexual dimorphism in limb bone size and robusticity appears to have reached recent human proportions.     

Long bones of the primate upper limb: Monomorphic or dimorphic?

An important debate has been taking place during the last few years concerningAustralopithecus afarensis: can the Hadar sample be ascribed to one highly dimorphic species or should it be separated into two distinct taxa? A similar problem occurs with the Middle Miocene cercopithecoids from East Africa: does this material belong to one dimorphic group or can we recognize two different taxa? The study of the long bones of the upper limb of many extant primates suggests that the extremities in different taxa are very distinctive but that within taxa the joints are weakly or are not morphologically dimorphic although they can be markedly size dimorphic. The main shape and size differences which can be ascribed to sexual dimorphism occur in the shafts of the long bones. Examinations have been made inHomo, Pan, Gorilla, Pongo, Hylobates, Alouatta, Cebus, Saimiri, Ateles, Nasalis, Presbytis and some Cercopithecinae. It appears, then, that the extremities of the bones are shape monomorphic. If the same relationships occurred in the fossil record, then the differences observed in the hominid fossil elbow joints at Hadar suggest that at least two different taxa are represented in the collection. In addition, among the cercopithecoid material assigned toVictoriapithecus from Maboko and Nyakach in East Africa, we recognize two distinct elbow morphologies indicating that two different taxa occur in the localities.     

Locomotor kinetics on sloped arboreal and terrestrial substrates in a small quadrupedal mammal

Small animals must be capable of moving on a wide variety of surfaces; thus, examining the mechanics of locomotion on a wide variety of substrates is necessary to understand how the animal can utilize its habitat. Therefore, locomotor kinetics are examined on arboreal and terrestrial sloped substrates in the marsupial Monodelphis domestica (gray short-tailed opossum). Substrate reaction forces were measured as opossums moved across four trackways: 30 degrees upslope and 30 degrees downslope trackways, which were flat ("terrestrial") or cylindrical ("arboreal"). Regardless of substrate slope, medial limb forces were measured on arboreal trackways and usually lateral limb forces on terrestrial trackways. Otherwise the general patterns of vertical and craniocaudal forces and impulses were similar between same-sloped terrestrial and arboreal trackways. Some significant modifications to these gross patterns occurred: on the arboreal upslope trackway, hindlimbs supported more body weight than on the terrestrial uphill, possibly because hindlimbs were more stably positioned on the upslope arboreal trackway than forelimbs. Furthermore, the difference between fore- and hindlimbs with respect to craniocaudal impulses was less on the arboreal sloped trackways. In conclusion, kinetic patterns can usually be explained by body weight support roles and by the placement of the limbs on the arboreal trackway.     

Differentiation between fore- and hindlimb bones and locomotor behaviour in primates

Primate appendicular limb bones were measured on the cross-sectional geometry at the mid-length of the humerus and femur and on the external dimensions of long bones of the same individuals. Cross sections were directly measured by means of computer tomography or direct sectioning. The morphometry of bones and locomotor behaviour is discussed from the viewpoint of the functional differentiation between the fore- and hindlimbs. The primate group which daily adopted a relatively terrestrial locomotor type demonstrates robust forelimb bones compared with the group which adopted a fully arboreal locomotor type. In contrast, the arboreal group showed relatively large and long hindlimb bones. The difference resembled the previously reported comparison between terrestrial and arboreal groups among wholly quadrupedal mammals. Humans were more similar to the arboreal group than to the terrestrial group. Parameters of the cross-sectional geometry showed a slightly positive allometry in total primate species. Slopes of the parameters were explained by the influence of muscle force.     

Residual stress distribution in rabbit limb bones

The presence of the residual stresses in bone tissue has been noted and the authors have reported that there are residual stresses in bone tissue. The aim of our study is to measure the residual stress distribution in the cortical bone of the extremities of vertebrates and to describe the relationships with the osteon population density. The study used the rabbit limb bones (femur, tibia/fibula, humerus, and radius/ulna) and measured the residual stresses in the bone axial direction at anterior and posterior positions on the cortical surface. The osteons at the sections at the measurement positions were observed by microscopy. As a result, the average stresses at the hindlimb bones and the forelimb bones were 210 and 149 MPa, respectively. In the femur, humerus, and radius/ulna, the residual stresses at the anterior position were larger than those at the posterior position, while in the tibia, the stress at the posterior position was larger than that at the anterior position. Further, in the femur and humerus, the osteon population densities in the anterior positions were larger than those in the posterior positions. In the tibia, the osteon population density in the posterior position was larger than that in the anterior position. Therefore, tensile residual stresses were observed at every measurement position in the rabbit limb bones and the value of residual stress correlated with the osteon population density (r=0.55, P<0.01).     

Air trapping and arboreal locomotor adaptation in primates: a review of experiments on humans

A review was made of experiments on humans in which air trapping by glottis closure during three-dimensional movements were examined in four subjects including former Olympic gymnasts. In brachiation and horizontal bar exercises, the behaviour of the larynx was monitored with a fiberoptic endoscope, and EMG-data were recorded from shoulder muscles. The results revealed that immobilization of the polyaxial connection between the shoulder girdle and the thorax by air trapping occurs in phases of extreme loading of the upper limbs. The closure of the airway by the larynx in humans serves three functions: first, the prevention of errors in deglutition; second, the production of vocal sounds; third, the retention of air inside the thoracic cavity. The latter function, air trapping, allows the immobilization of the rib cage for the muscular fixation of the shoulder blade on the trunk in movements that imply unusually high external forces acting on the upper limbs. This morphological-functional innovation probably has been made when early mammals invaded the three dimensional arboreal habitat, because it gave the tree-dwelling early primates the device to anchor themselves by the arms alone and to avoid falling out of trees. The specific functional characteristic of primates is the hermetic closure of the vocal and vestibular folds by rapidly contracting muscles in the folds. So the closure of the glottis, which in humans seems primarily an adaptation to the production of vocal tones, seems to go back to the adaptation of Tertiary arboreal primates to movements in a three-dimensional environment. Our conclusions are in agreement with the results of other contributions to this volume.     

Kinematics of the cercopithecine foot on arboreal and terrestrial substrates with implications for the interpretation of hominid terrestrial adaptations

The stereotyped characterizations of quadrupedal foot postures were tested by examining the kinematics of the cercopithecine foot on arboreal and terrestrial supports. Strictly arboreal species were compared with semi-terrestrial species for Cercopithecus, Cercocebus, Lophocebus, and Papio, in semi-natural or experimental settings. Results indicate that the kinematics of the cercopithecine arboreal quadruped differ in degree from stereotypical expectations for an arboreal quadruped. The relatively extended, adducted limb movements of the cercopithecines and the emphasis on the central digit as the functional axis of the foot suggest convergence with terrestrial mammalian cursors, and differ from the platyrrhine or colobine arboreal quadruped. The characteristics of the quadrupedal terrestrial primate foot contrast with the very unique pattern seen in the hominid foot. These contrasts provide a new perspective from which to interpret the hominid adaptation, in which the functional axis has remained fixed between the first and second digits. This pattern differs from virtually all other terrestrial mammals. The influence of bipedalism on this functional pattern is examined.     

Primate locomotor pattern repetitions,program clocks,and orientation to light

Remarkable locomotor pattern repetitions by small nocturnal primates in 122-cm activity wheels occurred during 4-hour light cycles with simulated twilights. Some of the repetitions owed their genesis almost entirely to a night-to-night concurrence of endogenous timing programs. Others depended on strong tendencies of the animals to orient relative to the position of light sources and enclosure environment. Still others were based partly on influences of twilight illuminance level on speed of locomotion.In many aspects the primate locomotor behavior was very similar to that of previously studied rodents and carnivores.     

Hunting pressure modulates the composition and size structure of terrestrial and arboreal vertebrates in Amazonian forests

Overhunting is a leading contemporary driver of tropical forest wildlife loss. The absence or extremely low densities of large-bodied vertebrates disrupts plant-animal mutualisms and consequently degrades key ecosystem services. Understanding patterns of defaunation is therefore crucial given that most tropical forests worldwide are now “half-empty”. Here we investigate changes in vertebrate community composition and size structure along a gradient of marked anthropogenic hunting pressure in the Médio Juruá region of western Brazilian Amazonia. Using a novel camera trapping grid design deployed both in the understorey and the forest canopy, we estimated the aggregate biomass of several functional groups of terrestrial and arboreal species at 28 sites along the hunting gradient. Generalized linear models (GLMs) identified hunting pressure as the most important driver of aggregate biomass for game, terrestrial, and arboreal species, as well as nocturnal rodents, frugivores, and granivores. Local hunting pressure affected vertebrate community structure as shown by both GLM and ordination analyses. The size structure of vertebrate fauna changed in heavily hunted areas due to population declines in large-bodied species and apparent compensatory increases in nocturnal rodents. Our study shows markedly altered vertebrate community structure even in remote but heavily settled areas of continuous primary forest. Depletion of frugivore and granivore populations, and concomitant density-compensation by seed predators, likely affect forest regeneration in persistently overhunted tropical forests. These findings contribute to a better understanding of how cascading effects induced by historical defaunation operate, informing wildlife management policy in tropical peri-urban, rural and wilderness areas.