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D L Gebo

Publications and source records attributed to D L Gebo.

16 recordsLinked to original sources

Middle Eocene primate tarsals from China: implications for haplorhine evolution.

We describe tarsal remains of primates recovered from the Middle Eocene (approximately 45 mya) Shanghuang fissures in southern Jiangsu Province, China. These tarsals document the existence of four higher-level taxa of haplorhine primates and at least two adapid species. The meager and poorly preserved adapid material exhibits some similarities to European adapines like Adapis. The haplorhine primates are divided into two major groups: a "prosimian group" consisting of Tarsiidae and an unnamed group that is anatomically similar to Omomyidae; and an "anthropoid group" consisting of Eosimiidae and an unnamed group of protoanthropoids. The anthropoid tarsals are morphologically transitional between omomyids (or primitive haplorhines) and extant telanthropoids, providing the first postcranial evidence for primates which bridge the prosimian-anthropoid gap. All of the haplorhines are extremely small (most are between 50-100 g), and the deposits contain the smallest euprimates ever documented. The uniqueness of this fauna is further highlighted by the fact that no modern primate community contains as many tiny primates as does the fauna from Shanghuang.

Animals↗

The oldest known anthropoid postcranial fossils and the early evolution of higher primates.

The middle Eocene primate family Eosimiidae, which is known from sites in central and eastern China and Myanmar, is central to efforts to reconstruct the origin and early evolution of anthropoid or 'higher' primates (monkeys, apes and humans). Previous knowledge of eosimiid anatomy has been restricted to the dentition and an isolated petrosal bone, and this limited anatomical information has led to conflicting interpretations of early anthropoid phylogeny. Here we describe foot bones of Eosimias from the same middle Eocene sites in China that yield abundant dental remains of this primate. Tarsals of Eosimias show derived anatomical traits that are otherwise restricted to living and fossil anthropoids. These new fossils substantiate the anthropoid status of Eosimias and clarify the phylogenetic position of anthropoids with respect to other major primate clades. Early anthropoids possessed a mosaic of primitive and derived traits in their postcranial skeletons, reflecting their derivation from haplorhine ancestors that retained many prosimian-like features.

Animals↗

A hominoid genus from the early Miocene of Uganda.

Fossils from a large-bodied hominoid from early Miocene sediments of Uganda, along with material recovered in the 1960s, show features of the shoulder and vertebral column that are significantly similar to those of living apes and humans. The large-bodied hominoid from Uganda dates to at least 20.6 million years ago and thus represents the oldest known hominoid sharing these derived characters with living apes and humans.

Animals↗

Climbing, brachiation, and terrestrial quadrupedalism: historical precursors of hominid bipedalism.

The vertical-climbing account of the evolution of locomotor behavior and morphology in hominid ancestry is reexamined in light of recent behavioral, anatomical, and paleontological findings and a more firmly established phylogeny for the living apes. The behavioral record shows that African apes, when arboreal, are good vertical climbers, and that locomotion during traveling best separates the living apes into brachiators (gibbons), scrambling/ climbing/brachiators (orangutans), and terrestrial quadrupeds (gorillas and chimpanzees). The paleontological record documents frequent climbing as an ancestral catarrhine ability, while a reassessment of the morphology of the torso and forelimb in living apes and Atelini suggests that their shared unique morphological pattern is best explained by brachiation and forelimb suspensory positional behavior. Further, evidence from the hand and foot points to a terrestrial quadrupedal phase in hominoid evolution prior to the adoption of bipedalism. The evolution of positional behavior from early hominoids to hominids appears to have begun with an arboreal quadrupedal-climbing phase and proceeded though an orthograde, brachiating, forelimb-suspensory phase, which was in turn followed by arboreal and terrestrial quadrupedal phases prior to the advent of hominid bipedality. The thesis that protohominids climbed down from the trees to become terrestrial bipeds needs to be reexamined in light of a potentially long history of terrestriality in the ancestral protohominid.

Animals↗

Habitat, annual, and seasonal effects on positional behavior in red colobus monkeys.

Positional behavior in adult red colobus monkeys (Colobus badius) was examined in a variety of ecological contexts. Using a focal-animal methodology, we assessed how data collected by different observers, in different years, in different seasons, and in different forests affected estimates of positional behavior. In all, 23,000 bouts were recorded. Variation in frequency is greatest in the common behaviors, especially arboreal quadrupedalism. Significant behavioral differences occur more often in the context of different forests than in annual or seasonal comparisons. The activity of feeding exhibits the largest frequency changes across positional behavior and ecological context. In all, red colobus monkeys exhibit substantial amounts of flexibility in positional behavior across different ecological contexts.

Animals↗

Positional behavior in five sympatric Old World monkeys.

Observations of positional behavior and habitat use were recorded on focal individuals of five species of Old World monkeys at Kibale Forest, Uganda, through the dry season of 1990 and 1991. Cercopithecus ascanius, Cercopithecus mitis, Cercocebus albigena, Colobus badius, and Colobus guereza commonly utilize five similar types of positional behavior (i.e., quadrupedalism, leaping, climbing, sitting, and standing), but in varying frequencies and situations. As a group, colobines use oblique supports and leap more often, and cover greater linear distances during leaps than do cercopithecines. Colobines also prefer to sit (about 90% of all postures), while cercopithecines stand more frequently. Body size differences between the sexes of a species are not reflected in positional behavior. The two small-bodied species climb more and leap less often than the three larger species, which is the reverse of what we would expect. Leaping is the most common method of crossing open spaces within the canopy; but most spatial gaps and leaps are over short distances, usually one meter or less. All five species, regardless of body size or the availability of forest supports, prefer medium-sized supports. Incorporating our work from Uganda with previous investigations of positional behavior reveals few consistent trends with respect to body size or habitat use across primates.

Animals↗

Terrestrial adaptations in the postcranial skeletons of guenons.

Arboreal and semiterrestrial guenons show similar osteological features of the limbs across a wide range of species, environments, and geography, while the more terrestrially committed guenons exhibit greater morphological divergence. An ecomorphological comparison of two sympatric guenons living in Kibale Forest, Uganda, reveals an array of anatomical adaptations for terrestriality in the limbs of Cercopithecus lhoesti similar to those found in Erythrocebus patas. In contrast, Cercopithecus aethiops, although also frequent users of the terrestrial environment, generally exhibit fewer morphological adaptations characteristic of a terrestrial lifestyle. It appears that significant morphological modification for terrestriality has occurred twice within the diverse radiation of living guenons with C. aethiops perhaps representing a third group in the making.

Adaptation, Biological↗

Plantigrady and foot adaptation in African apes: implications for hominid origins.

In living primates, except the great apes and humans, the foot is placed in a heel-elevated or semi-plantigrade position when these animals move upon arboreal or terrestrial substrates. Heel placement and bone positions in the non-great ape primate foot are designed to increase mobility and flexibility in the arboreal environment. Orangutans have further enhanced foot mobility by adapting their feet for suspension and thus similarly utilize foot positions where the heel does not touch the substrate. Chimpanzees and gorillas represent an alternative pattern (plantigrady), in which the heel contacts the surface of the support at the end of swing phase, especially during terrestrial locomotion. Thus, chimpanzees and gorillas possess feet adapted for both arboreal and terrestrial substrates. African apes also share several osteological features related to plantigrady and terrestrial locomotion with early hominids. From this analysis, it is apparent that hominid locomotor evolution passed through a quadrupedal terrestrial phase.

Adaptation, Physiological↗

Interrelationships among primate higher taxa.

One of the most controversial issues in primate palaeontology concerns the phylogenetic position of the extinct primate infraorder Adapiformes. During the Eocene, this group of primates of modern aspect possessed a holarctic distribution, and may have been present in the poorly known Palaeogene of Africa. Mainly on the basis of craniodental morphology, at least four hypotheses have been proposed concerning the phylogenetic interrelationships among adapiforms and other primate higher taxa: (1) that adapiforms are ancestral to both lemuriforms (including Lorisoidea) and anthropoids; (2) that adapiforms cannot be shown to possess a special phylogenetic relationship with either lemuriforms or anthropoids; (3) that adapiforms are the sister taxon of lemuriforms; and (4) that Adapiformes is not a natural, monophyletic group, but rather consists of nested clades within the radiation of lemuriforms. Here, we describe features of the ankle and wrist joints of several adapiform taxa that provide an independent test of the preceding hypotheses. These traits suggest that lemuriforms are monophyletic with respect to known adapiforms, but that adapiforms nevertheless are their stem lineage (sensu Ax).

Animals↗

Foot morphology and locomotor adaptation in Eocene primates.

Locomotor diversity of Eocene primates of North America and Europe was well developed, with species of both Adapidae and Omomyidae showing a wide spectrum of movements. Besides documenting the locomotor diversity in the Eocene, this paper shows that adapid foot morphology shares derived features with extant strepsirhines. Thus, the Omomyidae best resemble the ancestral euprimate in terms of foot morphology and locomotion. The generalized locomotor repertoire of the modern cheirogaleids represents the best model for the movement pattern of the ancestral euprimate.

Animals↗

A new species of Propliopithecus from the Fayum, Egypt.

Propliopithecus ankeli is described as a new species of hominoid from the early Oligocene of Egypt. The new species occurs at a stratigraphic level 80 m below quarries yielding P. chirobates and Aegyptopithecus zeuxis. P. ankeli differs from other species of the genus in its large size, relatively robust canines, larger and proportionally broader premolars, and M1 that has as great or greater mesiodistal length than M2. Thus, P. ankeli is characterized by increased relative size and robustness of the antemolar dentition, which contrasts with the pattern observed in the Fayum's other large hominoid, A. zeuxis. P. ankeli probably represents a lineage not ancestral to other Fayum hominoids. Discovery of this new species emphasizes the diversity of anthropoid primates that had already evolved by the early Oligocene.

Animals↗

Morphology and locomotor adaptations of the foot in early Oligocene anthropoids.

Newly discovered foot bones of Aegyptopithecus are described and compared to those of Apidium and Dolichocebus. Locomotor adaptations are inferred for African early Oligocene propliopithecids, parapithecids, and for Argentine early Oligocene Dolichocebus. All show an anthropoid grade of development in their foot anatomy. Tarsals of Aegyptopithecus compare best with those of Miocene hominoids. Apidium shares derived calcaneal features that link it with Old World monkeys. Dolichocebus exhibits a very generalized platyrrhine talar morphology akin to that seen in Saimiri, Callicebus, Cebus, and Aotus. The morphology of early Oligocene primate foot bones suggests that at least three quite distinct groups, corresponding to three recognized superfamilies, were present in the early Oligocene of South America and Africa.

Adaptation, Physiological↗

Puncture marks on early African anthropoids.

Field studies of living primates have shown that primate predation is a rare event. This must also have been true for past primate communities. In the Fayum Oligocene of Egypt, specimens of all four species of Upper Fossil Wood Zone primates show evidence of tooth puncture marks. Of the four potential groups of primate predators--the snakes, the raptors, the crocodiles, and the primitive carnivores or creodonts--only the crocodiles and the creodonts could have made these puncture marks. When one compares the feeding habits of living crocodiles and mammalian carnivores with the evidence from the Fayum, it appears that the Fayum primates were preyed upon and/or scavenged by mammalian carnivore-like animals. The dismemberment of the Fayum primates by Oligocene predators indicates, in part, why the Fayum fossil material is rarely articulated. Bone damage by predators may well set limits on what bone associations can be discovered in the Fayum even before the bones are scattered and buried by depositional processes.

Alligators and Crocodiles↗