Look in the trees: Hylobatids as evolutionary models for extinct hominins

Studying extant apes is of central importance to paleoanthropology. This approach is informative in inferring how hominin skeletal morphology reflects phylogeny, behavior, development, and ecological context. Traditionally, great apes have dominated the paleoanthropological literature as extant analogs for extinct hominins, to the exclusion of their phylogenetic sister group, the hylobatids. Phylogenetic proximity, large body size, and high encephalization quotients may have contributed to decisions to use great apes as models for hominins. However, if we reexamine hylobatids as extant models for extinct hominins—using modern phylogenetic, behavioral, and ecological data—this clade is uniquely poised to inform future frameworks in paleoanthropology. The following features make hylobatids strong analogs for extinct hominins: taxonomic diversity, the timing of diversification, hybridization between species, small body size, and reduced sexual dimorphism. Based on these shared features, hylobatids offer future opportunities to paleoanthropology, and provide a much richer extant analog than is currently recognized.     

Hominoid seminal protein evolution and ancestral mating behavior

Hominoid mating systems show extensive variation among species. The degree of sexual dimorphism in body size and canine size varies among primates in accordance with their mating system, as does the testes size and the consistency of ejaculated semen, in response to differing levels of sperm competition. To investigate patterns of evolution at hominoid seminal proteins and to make inferences regarding the mating systems of extinct taxa, we sequenced the entire coding region of the prostate-specific transglutaminase (TGM4) gene in human, chimpanzee, bonobo, western lowland gorilla, eastern lowland gorilla, orangutan, and siamang, including multiple humans, chimps, and gorillas. Partial DNA sequence of the coding regions was also obtained for one eastern lowland gorilla at the semenogelin genes (SEMG1 and SEMG2), which code for the predominant proteins in semen. Patterns of nucleotide variation and inferred protein sequence change were evaluated within and between species. Combining the present data with previous studies demonstrates a high rate of amino acid substitutions, and low intraspecific variation, at seminal proteins in Pan, presumably driven by strong sperm competition. Both gorilla species apparently possess nonfunctional TGM4, SEMG1, and SEMG2 genes, suggesting that gorillas have had low sperm competition, and therefore their current polygynous mating system, for a long time before their divergence. Similarly, orangutans show longstanding stasis at TGM4, which may be interpreted as evidence for an unchanging mating system for most of their evolution after their divergence from African apes. In contrast to the great apes, the data from humans could be interpreted as evidence of fluctuations between different mating systems or alternatively as a relaxed functional constraint in these proteins. It is our hope that this study is a first step toward developing a model to predict ancestral mating systems from extant molecular data to complement interpretations from the fossil record.     

Variability and sexual dimorphism in canine size of Australopithecus and extant hominoids

Among extant hominoids degrees of sexual dimorphism and combined-sex coefficients of variation of canine teeth dimensions are highly correlated. Based on this relationship and coefficients of variation of four species of the genus Australopithecus, we predict degrees of canine dimorphism for these extinct hominids. The estimates show that A. afarensis is as dimorphic as the pygmy chimpanzee, A. boisei slightly less dimorphic than the pygmy chimpanzee, A. robustus slightly more dimorphic than the lar gibbon, while A. africanus overiaps with the lar gibbon as well as a modern human sample. These estimates represent degrees of canine dimorphism substantially lower than results based upon prior sexing of individual specimens. The relationship between canine dimorphism and body weight dimorphism is also analyzed. All four species of Australopithecus are considerably less dimorphic in canine size for their body weight dimorphism than expected. This dissociation of canine size dimorphism and body weight dimorphism is shared with modern humans, and thus represents a unique hominid trait. We interpret the moderate to strong body weight dimorphism in australopithecines as the result of intra- and intersexual selection typical of a polygynous mating structure, while the rather mild canine dimorphism is interpreted in terms of the “developmental crowding” model for reduction in canine size.     

Sexual dimorphism in large-bodied primates: The case of the subfossil lemurs

Large body size has evolved repeatedly in the order Primates, not merely among anthropoids but also among prosimians. Whereas high degrees of sexual size dimorphism characterize many of the large-bodied anthropoids, this is not the case for extinct large-bodied lemurs. This paper uses finite mixture analysis and other techniques to ascertain just how much skull length dimorphism might be embedded in the generally unimodal distributions of skull lengths of giant extinct lemurs from single localities, and then compares these results with known skull length dimorphisms in extant lemurs and large-bodied catarrhines. We show that low levels of skull length sexual dimorphism (or none at all) characterize subfossil lemurs, and we explore several possible explanations for this phenomenon. Traditional explanations of sexual size dimorphism generally focus on body size or mating systems. These are not sufficient to explain the variation in sexual dimorphism that can be observed in the order Primates. © 1993 Wiley-Liss, Inc.     

The origins of sexual dimorphism in body size in ungulates

Jarman (1974) proposed a series of relationships between habitat use, food dispersion, and social behavior and hypothesized a series of evolutionary steps leading to sexual dimorphism in body size through sexual selection in African antelope species. The hypothesis states that sexual size dimorphism evolved in a three-step process. Initially, ancestral monomorphic and monogamous ungulate species occupying closed habitats radiated into open grassland habitats. Polygynous mating systems then rapidly evolved in response to the aggregation of males and females, perhaps in relation to the clumped distribution of food resources in open habitats. Subsequently, size dimorphism evolved in those species occupying open habitats, but not in species that remained in closed habitats or retained monogamy. This hypothesis has played an important role in explaining the origins of sexual dimorphism in mammals. However, the temporal sequence of the events that Jarman proposed has never been demonstrated. Here we use a phylogeny of extant ungulate species, along with maximum-likelihood statistical techniques, to provide a test of Jarman's hypothesis.     

A new species of Zorotypus (Insecta,Zoraptera, Zorotypidae) and the earliest known suspicious mating behavior of Zorapterans from the mid‐cretaceous amber of northern Myanmar

A new species of the insect order Zoraptera, Zorotypus pusillus, sp. n., is described and illustrated based on two ill‐preserved specimens in mid‐Cretaceous amber from the Hukawng Valley in northern Myanmar. Compared with known extinct zorapterans, the new species possesses eight‐segmented antennae and can be readily distinguished from all other extinct and recent members of the order in the presence of a shallow groove connecting two antennal sockets and by unique spination of the metafemur and metatibia. The earliest known suspicious mating behavior of Zoraptera, the intromittent organ of the fossil zorapterans, the egg, and the earliest known basal plate of the male genitalia are briefly discussed. The genitalia of new species are used as an intromittent organ in the majority of mating patterns among living zorapterans. The mating patterns (a copula is performed by males and females) of the most extant species have been present since at least the mid‐Cretaceous. A shared similar aedeagal structure in the new species and in the most extant species suggests an analogous mating behavior.     

Socioecology and the ontogeny of sexual size dimorphism in anthropoid primates

This study examines statistical correlations between socioecological variables (including measures of group composition, intermale competition, and habitat preference) and the ontogeny of body size sexual dimorphism in anthropoid primates. A regression-based multivariate measure of dimorphism in body weight ontogeny is derived from a sample of 37 species. Quantitative estimates of covariation between socioecological variables and this multivariate measure are evaluated. Statistically significant covariation between the ontogeny of dimorphism and socioecological variables, with the possible exception of habitat preference, is observed. Sex differences in ontogeny are lacking in species that exhibit low levels of intermale competition and are classifiable as species with monogamous/polyandrous mating systems. Among dimorphic species, two modes of dimorphic growth are apparent, which seem to be related to different kinds of group compositions. Multimale/multifemale species tend to become dimorphic through bimaturism (sex differences in duration of growth) with minimal sex differences in growth rate. Single-male/multifemale species tend to attain dimorphism through differences in rate of growth, often with limited bimaturism. Measures of intermale competition may also covary with these modes of dimorphic growth, but the relations among these variables are sometimes ambiguous. Correlations between dimorphic growth and behavioral variables may reflect alternative life history strategies in primates. Specifically, the ways in which risks faced by subadult males are distributed and the relations of these risks to growth rates seem to influence the evolution of size ontogenies. The absence of dimorphic ontogeny in some species can be tied to similar distributions of risk in each sex. In taxa that become dimorphic primarily through rate differences in growth, the lifetime distribution of risks for males may change rapidly. In contrast, males may face a pattern of uniformly changing or stable risk in species that become dimorphic through bimaturism. Finally, much variation recorded by this study remains unexplained, providing additional evidence of the need to specially examine female ontogeny before primate body size dimorphism can be satisfactorily explained. © 1995 Wiley-Liss, Inc.     

ESTIMATING SPECIATION AND EXTINCTION RATES FROM DIVERSITY DATA AND THE FOSSIL RECORD

Understanding the processes that underlie biodiversity requires insight into the evolutionary history of the taxa involved. Accurate estimation of speciation, extinction, and diversification rates is a prerequisite for gaining this insight. Here, we develop a stochastic birth–death model of speciation and extinction that predicts the probability distribution of both extinct and extant numbers of species in a clade. We present two estimation methods based on this model given data on the number of extinct species (from the fossil record) and extant species (from diversity assessments): a multivariate method of moments approach and a maximum-likelihood approach. We show that, except for some special cases, the two estimation methods produce very similar estimates. This is convenient, because the usually preferred maximum-likelihood approach is much more computationally demanding, so the method of moments can serve as a proxy. Furthermore, we introduce a correction for possible bias that can arise by the mere fact that we will normally only consider extant clades. We find that in some cases the bias correction affects the estimates profoundly. Finally, we show how our model can be extended to incorporate incomplete preservation. Preservation rates can, however, not be reliably estimated on the basis of numbers of extant and extinct species alone.     

Body mass in large extant and extinct carnivores

Body mass in six species of Plio-Pleistocene carnivores was estimated based on the relationship between mass and cross-sectional geometric properties, distal articular surface area, lengths and circumferences of proximal limb bones (femur and humerus) in 28 species of extant carnivores. All measures, except lengths, were found to give congruent body mass estimates. Two of the extinct carnivores ( Smilodon fatalis and Panthera atrox ) are estimated to be as much as one and a half times heavier than previously thought. Based on these results inferences are made concerning possible prey species.     

Taxonomic variation in the patterns of craniofacial dimorphism in primates

Understanding sexual dimorphism in living primates is important for interpreting the biological and taxonomic significance of variation in the primate fossil record. In the past two decades, there has been an increasing emphasis on the fact that sexual dimorphism varies in both magnitude and pattern among species. Several studies have suggested that distinct patterns of dimorphism may assist in species recognition and perhaps phylogenetic analysis. This study evaluates patterns of craniofacial dimorphism in samples of 82 anthropoid primates. Dimensions of the viscerocranium tend to be more dimorphic than those of the neurocranium and orbits. Principal components analysis of phylogenetically controlled data demonstrates a basic pattern of dimorphism in overall skull proportions, and a distinction between length and breadth measurements. For any given species there can be substantial variation in the magnitude of dimorphism among dimensions, and different species can show substantially different patterns of dimorphism within and between regions of the skull and jaws. Patterns of dimorphism are clearly associated with phylogeny. Pattern similarity is not dependent on the overall magnitude of craniofacial dimorphism, or body mass dimorphism. Among all anthropoids, there are few combinations of characters that consistently show greater or lesser degrees of dimorphism. Such "stability" of patterns increases within genera. Patterns of dimorphism are likely to be useful for interpreting the taxonomic significance of variation in the fossil record. However, phylogenetic propinquity alone is not reason to use an extant species as a model for variation in an extinct species. Rather, care must be taken to identify stable patterns of dimorphism within a group of closely related extant species.     

Digit ratios predict polygyny in early apes, Ardipithecus, Neanderthals and early modern humans but not in Australopithecus

Social behaviour of fossil hominoid species is notoriously difficult to predict owing to difficulties in estimating body size dimorphism from fragmentary remains and, in hominins, low canine size dimorphism. Recent studies have shown that the second-to-fourth digit ratio (2D : 4D), a putative biomarker for prenatal androgen effects (PAEs), covaries with intra-sexual competition and social systems across haplorrhines; non-pair-bonded polygynous taxa have significantly lower 2D : 4D ratios (high PAE) than pair-bonded monogamous species. Here, we use proximal phalanx ratios of extant and fossil specimens to reconstruct the social systems of extinct hominoids. Pierolapithecus catalaunicus, Hispanopithecus laietanus and Ardipithecus ramidus have ratios consistent with polygynous extant species, whereas the ratio of Australopithecus afarensis is consistent with monogamous extant species. The early anatomically modern human Qafzeh 9 and Neanderthals have lower digit ratios than most contemporary human populations, indicating increased androgenization and possibly higher incidence of polygyny. Although speculative owing to small sample sizes, these results suggest that digit ratios represent a supplementary approach for elucidating the social systems of fossil hominins.     

Strong postcranial size dimorphism in Australopithecus afarensis: results from two new resampling methods for multivariate data sets with missing data

There is considerable debate over the level of size dimorphism and inferred social behavior of Australopithecus afarensis. Most previous studies have analyzed size variation in single variables or multiple variables drawn from single elements. These approaches suffer from small sample sizes, underscoring the need for new techniques that incorporate measurements from multiple unassociated elements, reducing the influence of random sampling on size variation in fossil samples. One such technique, the template method, has recently been proposed but is limited to samples with a template specimen and is sensitive to a number of assumptions. Here we present two new resampling methods that do not require a template specimen, allow measurements from multiple unassociated elements to be included in a single analysis, and allow for significance tests between comparative and fossil multivariate data sets with missing data. Using these new methods, multivariate postcranial size dimorphism is measured using eight measurements of the femur, tibia, humerus, and radius in samples of A. afarensis, modern humans, chimpanzees, gorillas, and orangutans. Postcranial dimorphism in A. afarensis is similar to that of gorillas and orangutans, and significantly greater than in modern humans and chimpanzees. Because studies in living primates have examined the association of behavior with dimorphism in body mass and craniodental measurements, not postcrania, relationships between postcranial dimorphism and social behavior must be established to make robust behavioral inferences for A. afarensis. However, the results of this and past studies strongly suggest behavioral and mating strategies differed between A. afarensis and modern humans.     

The role of time and timing in hominid dental evolution

Exactly when during evolution hominids acquired their extended extra-uterine growth period is a contentious issue. In order to shed light on the tempo and mode of ontogenetic changes during hominid evolution, research has focused on the pattern and, to a lesser extent, the rate of growth observed in the developing dentition of extant and extinct hominoid taxa. From these data, the absolute timing of events has often been inferred, either implicitly or explicitly. Differences in patterns of growth, especially of the eruption of teeth, are reasonably well documented among hominoids. However, data on the absolute timing of dental developmental events are much more scarce, rendering tentative all inferences about timing from patterns alone. Such inferences are even more tentative when they involve interpreting ontogenetic trajectories in extinct species such as Plio-Pleistocene hominids, which almost certainly had unique patterns of maturation. In order to contribute to the debate about possible relations between pattern and timing in the developing dentition, we have collated information that specifically relates to the absolute timing of developmental events in extant and extinct hominoids and, hence, also to the rate at which processes occur. In doing so, we have attempted to identify both developmental constraints and possible heterochronic processes that may have led to the extended growth period characteristic of humans. There appears to be growing evidence that evolution toward an extended hominid ontogeny did not follow a path that can be described as a simple heterochronic event.     

Back-casting sociality in extinct species: new perspectives using mass death assemblages and sex ratios

Despite 150 years of interest in the ecology of dinosaurs, mammoths, proto-hominids and other extinct vertebrates, a general framework to recreate patterns of sociality has been elusive. Based on our recent discovery of a contemporary heterospecific mass death assemblage in the Gobi Desert (Mongolia), we fit predictions about gender-specific associations and group living in extant ungulates to extinct ones. We relied on comparative data on sex-ratio variation and body-size dimorphism, basing analyses on 38 additional mass mortality sites from Asia, Africa, Europe and North America that span 50 million years. Both extant and extinct species died in aggregations with biased adult sex ratios, but the skew (from 1:1) was greater for extinct dimorphic taxa, suggesting that sociality in these extinct species can be predicted from spatial and demographic traits of extant ones. However, extinct rhinos, horses and zebras were inconsistent with predictions about adult sex ratios, which underscores the inherent difficulty in backcasting historic patterns to some monomorphic taxa. These findings shed light not only on the sociality of extinct species but provide a sound, although limited, footing for interpretation of modern death assemblages within the context of the emerging science of taphonomy and palaeobehaviour.     

Advantages and Limitations in the Use of Extant Xenarthrans (Mammalia) as Morphological Models for Paleobiological Reconstruction

Extant species of Xenarthra represent a severely restricted sample of the total diversity achieved by the group. Given their shared history, the extant representatives of the three major groups of xenarthrans (Cingulata, Folivora, and Vermilingua) provide a valuable basis for paleobiological inference. However, many extinct taxa are morphologically so dissimilar from their extant relatives that they suggest very different ways of life. In these cases, extinct forms do not have modern models within the group and the application of a simplistic and strict approach can produce nonsensical reconstructions. In this contribution, we evaluate the limitations of the use of extant xenarthrans as morphological models for paleobiological reconstructions. A database of linear dimensions of the appendicular skeleton of extant and extinct xenarthrans and other mammals (marsupials, carnivorans, rodents, primates, perissodactyls, artiodactyls, and proboscideans) was constructed. Exploratory analyzes were performed on general morphometric similarity between existing and extinct xenarthrans (PCA) and the accuracy of body mass estimates of extinct xenarthrans based on their close relatives and other mammals (simple and multiple linear regressions) were tested. Extinct xenarthrans occupy similar relative positions in the morphospaces as extant mammals other than their closest relatives. Most allometric equations, particularly those based only on xenarthrans, produced remarkable underestimates. This can be explained by dimensional differences (up to four orders of magnitude) and shape differences between most of the extinct and extant xenarthrans. This does not invalidate actualism and the use of analogues, but suggests the need to apply other approaches, such as mechanics, that address form-function relationships but are not necessarily based on known biological comparators.     

Similar Associations of Tooth Microwear and Morphology Indicate Similar Diet across Marsupial and Placental Mammals

Low-magnification microwear techniques have been used effectively to infer diets within many unrelated mammalian orders, but the extent to which patterns are comparable among such different groups, including long extinct mammal lineages, is unknown. Microwear patterns between ecologically equivalent placental and marsupial mammals are found to be statistically indistinguishable, indicating that microwear can be used to infer diet across the mammals. Microwear data were compared to body size and molar shearing crest length in order to develop a system to distinguish the diet of mammals. Insectivores and carnivores were difficult to distinguish from herbivores using microwear alone, but combining microwear data with body size estimates and tooth morphology provides robust dietary inferences. This approach is a powerful tool for dietary assessment of fossils from extinct lineages and from museum specimens of living species where field study would be difficult owing to the animal’s behavior, habitat, or conservation status.     

Scaling relationships between craniofacial sexual dimorphism and body mass dimorphism in primates: implications for the fossil record

Craniofacial remains (the most abundant identifiable remains in the fossil record) potentially offer important information about body size dimorphism in extinct species. This study evaluates the scaling relationships between body mass dimorphism and different measures of craniofacial dimorphism, evaluating taxonomic differences in the magnitude and scaling of craniofacial dimorphism across higher taxonomic groups. Data on 40 dimensions from 129 primate species and subspecies demonstrate that few dimensions change proportionally with body mass dimorphism. Primates show general patterns of greater facial vs. neurocranial and orbital dimorphism, and greater dimorphism in lengths as opposed to breadths. Within any species, though, different craniofacial dimensions can yield very different reconstructions of size dimorphism. There are significant taxonomic differences in the relationships between size and craniofacial dimorphism among primate groups that can have a significant impact on reconstructions of body mass dimorphism. Hominoids tend to show lower degrees of facial dimorphism proportional to size dimorphism than other primates. This in turn implies that strong craniofacial dimorphism in Australopithecus africanus could imply very strong body size dimorphism, conflicting with the relatively modest size dimorphism inferred from postcrania. Different methods of estimating the magnitude of size dimorphism from craniofacial measurements yield similar results, and yield comparatively low percent prediction errors for a number of dimensions. However, confidence intervals for most estimates are so large as to render most estimates highly tentative.     

Sexual dimorphism and mating systems: jumping to conclusions

Previous studies have suggested that there is a strong relationship between a high degree of aggressive competition among males for access to fertile females and large body and canine size in males. It has further been suggested that such a relationship among living primates can be used to infer the social organization of extinct primate species from the degree of sexual dimorphism exhibited. Our field studies of patas (Erythrocebus patas) and blue monkeys (Cercopithecus mitis), two species which had previously been characterized as having one-male ‘harem’ group structures, indicate considerable variability in mating systems. We suggest, on the basis of our observations of these species, that factors other than male-male competition (e.g., predation) may also have influenced the degree of dimorphism in primates.     

Metric variation and sexual dimorphism in the dentition of Ouranopithecus macedoniensis

The fossil sample attributed to the late Miocene hominoid taxon Ouranopithecus macedoniensis is characterized by a high degree of dental metric variation. As a result, some researchers support a multiple-species taxonomy for this sample. Other researchers do not think that the sample variation is too great to be accommodated within one species. This study examines variation and sexual dimorphism in mandibular canine and postcanine dental metrics of an Ouranopithecus sample. Bootstrapping (resampling with replacement) of extant hominoid dental metric data is performed to test the hypothesis that the coefficients of variation (CV) and the indices of sexual dimorphism (ISD) of the fossil sample are not significantly different from those of modern great apes. Variation and sexual dimorphism in Ouranopithecus M(1) dimensions were statistically different from those of all extant ape samples; however, most of the dental metrics of Ouranopithecus were neither more variable nor more sexually dimorphic than those of Gorilla and Pongo. Similarly high levels of mandibular molar variation are known to characterize other fossil hominoid species. The Ouranopithecus specimens are morphologically homogeneous and it is probable that all but one specimen included in this study are from a single population. It is unlikely that the sample includes specimens of two sympatric large-bodied hominoid species. For these reasons, a single-species hypothesis is not rejected for the Ouranopithecus macedoniensis material. Correlations between mandibular first molar tooth size dimorphism and body size dimorphism indicate that O. macedoniensis and other extinct hominoids were more sexually size dimorphic than any living great apes, which suggests that social behaviors and life history profiles of these species may have been different from those of living species.