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1.
Am J Phys Anthropol ; 171(1): 76-88, 2020 01.
Article En | MEDLINE | ID: mdl-31710703

OBJECTIVES: Here, we quantify and compare the cross-sectional shape of the mandibular corpus between M1 and M2 during growth in Pan paniscus, Pan troglodytes, and Pongo pygmaeus. The goal is to assess the hypothesis that the shape of the corpus is influenced by the development of permanent molars in their crypts, by examining ontogenetic changes in corpus shape and investigating covariation between corpus shape and M2 and M3 molar crypt forms. MATERIALS AND METHODS: Ontogenetic changes in mandibular corpus shape were assessed using landmarks and semilandmarks, and measurements of length, width, and height were used to quantify molar crypts (M2 and M3 ). Ontogenetic changes in corpus growth from the eruption of M1 to the eruption of M3 were evaluated for each species through generalized Procrustes analysis and principal components analysis in shape-space and form-space. The relationship between corpus shape and molar crypt form was investigated at three different developmental stages using two-block partial least squares (2B-PLS) analysis. RESULTS: The results show clear differences in growth patterns among all three species and provide evidence that species-level differences in mandibular corpus growth occur prior to the emergence of M1 . The results of the 2B-PLS analysis reveal that significant covariance between corpus shape and molar crypt form is limited to the developmental stage marked by the emergence of M1 , with covariance between corpus shape and M2 crypt width. Corpora that are relatively narrower in the inferior portion of the cross section covary with relatively narrower M2 crypts. CONCLUSIONS: These results have important implications for understanding the taxonomic and phylogenetic significance of mandibular corpus shape variation in the hominoid fossil record.


Mandible/growth & development , Molar/growth & development , Pan paniscus/growth & development , Pan troglodytes/growth & development , Pongo pygmaeus/growth & development , Animals , Mandible/anatomy & histology , Molar/anatomy & histology , Pan paniscus/anatomy & histology , Pan troglodytes/anatomy & histology , Pongo pygmaeus/anatomy & histology , Species Specificity
2.
J Comp Physiol B ; 189(6): 659-672, 2019 12.
Article En | MEDLINE | ID: mdl-31549180

Non-invasive measures of stress are crucial for captive and conservation management programs. The adrenal hormone dehydroepiandrosterone-sulfate (DHEAS) has recently been adopted as a stress marker, but there is little investigation of its relationship to glucocorticoids (GC), well-known indicators of stress. This study examined the influence of age, reproductive state and environment on GC and DHEAS levels in orangutans, to test whether the GC/DHEAS ratio can provide an index of stress response in primates. We measured fecal GC (fGC) and fecal DHEAS (fDHEAS) concentrations in 7 captive orangutans from zoological parks in Japan and 22 wild orangutans from Danum Valley Conservation Area, Malaysia. We found that in a stressful condition (transportation), fDHEAS levels increased 2 days after the fGC response, which occurred 1 day after the stressor. One pregnant female had elevated levels of both hormones, and a higher fGC/fDHEAS ratio than baseline. Females in the first year of lactation had fGC levels and the fGC/fDHEAS ratio significantly higher than both baseline and females in the second and subsequent years of lactation. There was no effect of age on fGC levels, but the fGC/fDHEAS ratio was higher in infants than adults and adolescents. fDHEAS concentrations were lower in infants than juveniles, adolescents and adults, a phenomenon known as adrenarche, shared with humans and other great apes. We suggest that changes in DHEAS during orangutan life history are associated with changes in the dynamics of maintaining homeostasis that vary with age and reproductive state. The GC/DHEAS ratio index is useful to evaluate age-related abilities of responding to stressful challenges.


Dehydroepiandrosterone/metabolism , Glucocorticoids/metabolism , Pongo pygmaeus/growth & development , Stress, Physiological , Age Factors , Animals , Animals, Wild , Animals, Zoo , Dehydroepiandrosterone/analogs & derivatives , Dehydroepiandrosterone/analysis , Dehydroepiandrosterone/chemistry , Feces/chemistry , Female , Glucocorticoids/analysis , Glucocorticoids/chemistry , Lactation/metabolism , Male , Pongo pygmaeus/physiology , Pregnancy
3.
Sci Rep ; 7(1): 4839, 2017 07 07.
Article En | MEDLINE | ID: mdl-28687788

For many threatened species the rate and drivers of population decline are difficult to assess accurately: species' surveys are typically restricted to small geographic areas, are conducted over short time periods, and employ a wide range of survey protocols. We addressed methodological challenges for assessing change in the abundance of an endangered species. We applied novel methods for integrating field and interview survey data for the critically endangered Bornean orangutan (Pongo pygmaeus), allowing a deeper understanding of the species' persistence through time. Our analysis revealed that Bornean orangutan populations have declined at a rate of 25% over the last 10 years. Survival rates of the species are lowest in areas with intermediate rainfall, where complex interrelations between soil fertility, agricultural productivity, and human settlement patterns influence persistence. These areas also have highest threats from human-wildlife conflict. Survival rates are further positively associated with forest extent, but are lower in areas where surrounding forest has been recently converted to industrial agriculture. Our study highlights the urgency of determining specific management interventions needed in different locations to counter the trend of decline and its associated drivers.


Endangered Species , Pongo pygmaeus/growth & development , Population Dynamics/trends , Animals , Borneo , Models, Statistical , Survival Analysis
4.
Primates ; 58(1): 211-224, 2017 01.
Article En | MEDLINE | ID: mdl-27600514

Orangutans have a long period of immaturity and the longest inter-birth interval (IBI) of all mammals, which can be explained by their solitary life style, preventing the mother from rearing two offspring simultaneously (solitary life hypothesis) [corrected]. We collected data on mother-offspring dyads living in a primary lowland forest in Danum Valley, East Borneo in an effort to examine the developmental and behavioral patterns of the subspecies Pongo pygmaeus morio. We analyzed developmental changes in mother-offspring distance, contact, and activity budgets in orangutans ranging from 1 to 7 years of age. The results indicated decreased resting and playing with increasing age, whereas feeding, traveling and social play all increased significantly. Mothers' feeding and traveling time were good predictors of their offspring's feeding and traveling activities. Mother-offspring contact lasted longer in resting contexts; contact during traveling was almost non-existent after 4 years of age. Comparisons with previously published data on the Sumatran species Pongo abelli revealed no fundamental differences in these behavioral measures. However, a shorter association time with the mother after behavioral independence is documented for this East Bornean population in comparison to Sumatran populations. These results are best explained by the solitary life hypothesis, in agreement with previous studies. We suggest that environmental constraints in Bornean forests, as well as a lower population density, should be considered when interpreting the differences between Sumatran and Bornean orangutans in both the period of association with mother and the IBI.


Feeding Behavior , Homing Behavior , Motor Activity , Pongo pygmaeus/physiology , Age Factors , Animals , Borneo , Female , Malaysia , Male , Mothers , Pongo pygmaeus/growth & development
5.
Am J Primatol ; 77(11): 1170-8, 2015 Nov.
Article En | MEDLINE | ID: mdl-26235914

Among primates, orangutans are unique in having pronounced male bimaturism leading to two fully adult morphs that differ in both physical appearance and behavior. While unflanged males have a female-like appearance, flanged males have the full suite of secondary sexual characteristics, including cheek flanges and a large throat sac. So far, hormonal correlates of arrested development in unflanged males and the expression of secondary sexual characteristics in flanged males have only been studied in zoo-housed individuals. In this study, we investigated fecal androgen and glucocorticoid metabolites as hormonal correlates of male bimaturism in 17 wild adult Bornean orangutans (Pongo pygmaeus) in Central Kalimantan, Indonesia. We predicted and found higher androgen levels in flanged males compared to unflanged males, probably due to ongoing strong competition among flanged males who meet too infrequently to establish a clear linear dominance hierarchy. Furthermore, we found no difference in fecal glucocorticoid metabolite concentrations between flanged and unflanged males, indicating that social stress is unlikely to explain arrested development in unflanged wild orangutans. The only actively developing male in our study showed significantly higher androgen levels during the period of development than later as a fully flanged male. This supports earlier findings from zoo studies that elevated androgen levels are associated with the development of secondary sexual characteristics.


Androgens/metabolism , Glucocorticoids/metabolism , Pongo pygmaeus/growth & development , Pongo pygmaeus/physiology , Animals , Feces/chemistry , Indonesia , Male , Sex Characteristics , Social Dominance
6.
PLoS One ; 5(9): e12813, 2010 Sep 22.
Article En | MEDLINE | ID: mdl-20877646

Ecological studies of orangutans have almost exclusively focused on populations living in primary or selectively logged rainforest. The response of orangutans to severe habitat degradation remains therefore poorly understood. Most experts assume that viable populations cannot survive outside undisturbed or slightly disturbed forests. This is a concern because nearly 75% of all orangutans live outside protected areas, where degradation of natural forests is likely to occur, or where these are replaced by planted forests. To improve our understanding of orangutan survival in highly altered forest habitats, we conducted population density surveys in two pulp and paper plantation concessions in East Kalimantan, Indonesia. These plantations consist of areas planted with fast-growing exotics intermixed with stands of highly degraded forests and scrublands. Our rapid surveys indicate unexpectedly high orangutan densities in plantation landscapes dominated by Acacia spp., although it remains unclear whether such landscapes can maintain long-term viable populations. These findings indicate the need to better understand how plantation-dominated landscapes can potentially be incorporated into orangutan conservation planning. Although we emphasize that plantations have less value for overall biodiversity conservation than natural forests, they could potentially boost the chances of orangutan survival. Our findings are based on a relatively short study and various methodological issues need to be addressed, but they suggest that orangutans may be more ecologically flexible than previously thought.


Ecosystem , Pongo pygmaeus/growth & development , Trees/growth & development , Animals , Conservation of Natural Resources , Population Density
7.
Mol Ecol ; 17(12): 2898-909, 2008 Jun.
Article En | MEDLINE | ID: mdl-18494768

We examined mitochondrial DNA control region sequences of 73 Kinabatangan orangutans to test the hypothesis that the phylogeographical structure of the Bornean orangutan is influenced by riverine barriers. The Lower Kinabatangan Wildlife Sanctuary contains one of the most northern populations of orangutans (Pongo pygmaeus) on Borneo and is bisected by the Kinabatangan River, the longest river in Sabah. Orang-utan samples on either side of the river were strongly differentiated with a high Phi(ST) value of 0.404 (P < 0.001). Results also suggest an east-west gradient of genetic diversity and evidence for population expansion along the river, possibly reflecting a postglacial colonization of the Kinabatangan floodplain. We compared our data with previously published sequences of Bornean orangutans in the context of river catchment structure on the island and evaluated the general relevance of rivers as barriers to gene flow in this long-lived, solitary arboreal ape.


DNA, Mitochondrial/genetics , Pongo pygmaeus/genetics , Animals , Ecosystem , Genetic Variation , Genetics, Population , Geography , Malaysia , Phylogeny , Pongo pygmaeus/classification , Pongo pygmaeus/growth & development , Sequence Analysis, DNA
8.
Am J Primatol ; 65(4): 353-76, 2005 Apr.
Article En | MEDLINE | ID: mdl-15834889

Orangutans display remarkable developmental changes and sexual differences in facial morphology, such as the flanges or cheek-pads that develop only on the face of dominant adult males. These changes suggest that facial morphology is an important factor in visual communication. However, developmental changes in facial morphology have not been examined in detail. We studied developmental changes in the facial morphology of the Borneo orangutan (Pongo pygmaeus) by observing 79 individuals of various ages living in the Sepilok Orangutan Rehabilitation Centre (SORC) in Malaysia and in Japanese zoos. We also analyzed photographs of one captive male that were taken over a period of more than 16 years. There were clear morphological changes that occurred with growth, and we identified previously unreported sexual and developmental differences in facial morphology. Light-colored skin around the eyes and mouth is most prominent in animals younger than 3 years, and rapidly decreases in area through the age of approximately 7 years. At the same time, the scattered, erect hairs on the head (infant hair) become thick, dense hairs lying on the head (adult hair) in both sexes. The results suggest that these features are infant signals, and that adult signals may include darkened face color, adult hair, whiskers, and a beard, which begin to develop after the age of approximately 7 years in both sexes. In females, the eyelids remain white even after 10 years, and turn black at around the age of 20; in males, the eyelids turn black before the age of 10. The whiskers and beards of adults are thicker in males than in females, and are fully developed before the age of 10 in males, while they begin to develop in females only after approximately 20 years. White eyelids and undeveloped whiskers and beards may be visual signals that are indicative of young adult females. Our results also show that the facial morphology of the unflanged male is similar to that of the adult female, although it has also been pointed out that unflanged males resemble younger individuals.


Face/anatomy & histology , Pigmentation/physiology , Pongo pygmaeus/anatomy & histology , Pongo pygmaeus/growth & development , Age Factors , Animals , Hair/anatomy & histology , Hair/growth & development , Hair/physiology , Malaysia , Photography , Sex Factors , Skin Physiological Phenomena , Statistics, Nonparametric
9.
Am J Primatol ; 65(2): 149-66, 2005 Feb.
Article En | MEDLINE | ID: mdl-15706586

The orangutan is widely recognized as a highly dimorphic species. An ontogenetic approach to the study of sexual dimorphism can assist researchers in understanding both where and when these differences develop. In this study, 357 orangutans from Borneo were divided into five developmental stages representing infancy to mature adulthood. Three-dimensional (3D) coordinate data from 16 landmarks representing the face and palate were analyzed by means of a Euclidean distance matrix analysis (EDMA), a quantitative method for the comparison of forms. Three separate analyses (an age-specific static comparison of forms, a sex-specific analysis of growth trajectories, and an intersex comparison of patterns of relative growth) were carried out with the intent to describe the rate, timing, magnitude, and pattern of growth in the orangutan face and palate. The results indicate that generally males and females share a similar, but not identical, pattern of growth or local form change, but differ in growth rate, timing, and magnitude of difference. Dimorphism in the face and palate can be localized in infancy and traced throughout all age intervals. Orangutan females grow slightly faster than males from infancy to adolescence, at which time male growth exceeds female growth. Female growth ceases with the advent of adulthood, while male growth continues (i.e., both the number and magnitude of the dimorphic dimensions increase). Males and females are similar in facial dimensions and growth related to the orbits, upper face, and palate width. They maintain these similarities throughout development. However, they differ in facial and nasal height, palate length, snout projection, depth of the nasopharynx, and hafting of the face onto the skull. The face broadens and the zygomatic bone flares dramatically in adult males, corresponding to the development of cheek pads. While growth patterns are similar between the two sexes, they differ in the lateral orbit, snout projection, and hafting of the face onto the cranium. Adult dimorphism is the result of growth patterns experienced throughout life, and it is not equally expressed across the cranium. An understanding of patterns of dimorphism, along with the magnitude of difference, may be helpful for interpreting dimorphism in the fossil record.


Face/anatomy & histology , Palate/anatomy & histology , Pongo pygmaeus/anatomy & histology , Sex Characteristics , Animals , Face/physiology , Female , Male , Palate/growth & development , Pongo pygmaeus/growth & development
10.
J Hum Evol ; 47(6): 385-98, 2004 Dec.
Article En | MEDLINE | ID: mdl-15566945

We present life history data on wild Sumatran orangutans gleaned from a 32-year and a 5.5-year study. Estimated age at first reproduction was 15.4 years. At 9.3 years, the average interbirth interval for this population is the longest ever recorded for any great ape population, significantly longer than that of a Bornean orangutan population. We find that age-specific mortality of Sumatran orangutans does not differ between sexes and is significantly lower than that of wild chimpanzees. We conclude that orangutan life history is the slowest among extant great apes. In accordance with their slow life history, longevity in the wild is estimated to be at least 58 years for males and at least 53 for females. We find no evidence for menopause. These data suggest that compared to the ancestral state, humans have undergone less of an increase in longevity than commonly assumed, and have experienced selection on earlier cessation of reproduction.


Pongo pygmaeus/physiology , Animals , Biological Evolution , Female , Humans , Indonesia , Life Tables , Longevity/physiology , Male , Pan troglodytes/growth & development , Pongo pygmaeus/growth & development , Pregnancy , Reproduction/physiology , Sex Ratio
11.
J Hum Evol ; 46(6): 679-97, 2004 Jun.
Article En | MEDLINE | ID: mdl-15183670

Molecular data suggest that humans are more closely related to chimpanzees than either is to the gorillas, yet one finds the closest similarity in craniofacial morphology to be among the great apes to the exclusion of humans. To clarify how and when these differences arise in ontogeny, we studied ontogenetic trajectories for Homo sapiens, Pan paniscus, Pan troglodytes, Gorilla gorilla and Pongo pygmaeus. A total of 96 traditional three-dimensional landmarks and semilandmarks on the face and cranial base were collected on 268 adult and sub-adult crania for a geometric morphometric analysis. The ontogenetic trajectories are compared by various techniques, including a new method, relative warps in size-shape space. We find that adult Homo sapiens specimens are clearly separated from the great apes in shape space and size-shape space. Around birth, Homo sapiens infants are already markedly different from the great apes, which overlap at this age but diverge among themselves postnatally. The results suggest that the small genetic differences between Homo and Pan affect early human ontogeny to induce the distinct adult human craniofacial morphology. Pure heterochrony does not sufficiently explain the human craniofacial morphology nor the differences among the African apes.


Hominidae/anatomy & histology , Hominidae/growth & development , Skull/anatomy & histology , Skull/growth & development , Adult , Animals , Anthropometry/methods , Child , Female , Gorilla gorilla/anatomy & histology , Gorilla gorilla/growth & development , Humans , Infant , Male , Pan paniscus/anatomy & histology , Pan paniscus/growth & development , Pan troglodytes/anatomy & histology , Pan troglodytes/growth & development , Pongo pygmaeus/anatomy & histology , Pongo pygmaeus/growth & development
12.
Am J Phys Anthropol ; 118(1): 25-32, 2002 May.
Article En | MEDLINE | ID: mdl-11953942

Both in the wild and in captivity, a marked and enduring arrest of secondary sexual developmental occurs in some male orangutans (Pongo pygmaeus) (Kingsley [1982] The Orang-Utan: Its Biology and Conservation, The Hague: Junk; Utami [2000]). Researchers have hypothesized that chronic stress, perhaps related to aggression from mature males, causes endocrine changes altering growth and maturation rates in these males (Maple [1980] Orangutan Behavior, New York: Van Nostrand Reinhold; Graham [1988] Orangutan Biology, Oxford: Oxford University Press). In this study, urine samples were collected over a 3-year period from 23 captive male orangutans to test the hypothesis that developmentally arrested male orangutans have an endocrine profile consistent with chronic stress. Three study males were juveniles, seven were arrested adolescents, six were developing adolescents, and seven were mature adults. Morning samples were analyzed by radioimmunoassay for levels of the stress hormones cortisol and prolactin, and group hormone profiles were compared by analysis of variance. Results indicate that developing adolescent male orangutans have a significantly higher stress hormone profile than juvenile, developmentally arrested adolescent, or adult males. These results imply that the arrest of secondary sexual development in some male orangutans is not stress-induced, but instead perhaps an adaptation for stress avoidance during the adolescent or "subadult" period. These data, together with previously reported data on levels of gonadotropins, testicular steroids, and growth-related hormones, define endocrine profiles associated with alternative reproductive strategies for males with and males without secondary sexual features (Maggioncalda et al. [1999], [2000].


Disorders of Sex Development/psychology , Disorders of Sex Development/veterinary , Pongo pygmaeus/growth & development , Sexual Maturation/physiology , Stress, Psychological , Animals , Hydrocortisone/urine , Male , Prolactin/urine
13.
Am J Primatol ; 50(1): 67-76, 2000 Jan.
Article En | MEDLINE | ID: mdl-10588436

There are two morphs of reproductive male in orangutans. Both morphs span the age range from adolescent to adult, but "subadult" males are smaller in size and lack secondary sexual features. In this study, urine samples were collected over a 2 year period from 23 captive male orangutans in order to define the endocrinology of this apparent arrest of secondary sexual development. Three males were juveniles, 3 to 5 years of age; seven males showed no secondary sexual trait development and were over 7 years of age; six males were in the process of developing secondary sexual features, with the youngest male being 6 years of age; and seven males were fully mature adults. Morning samples were analyzed by radioimmunoassay for levels of growth hormone (GH) and thyroid-stimulating hormone (TSH) and group hormone profiles were compared by analysis of variance. GH is the primary hormone of growth and development and its increase in teenage boys is associated with the adolescent growth spurt. TSH stimulates the thyroid to produce and secrete hormones that have metabolic effects and required for normal growth and development. Results show that arrested adolescent male orangutans have a GH level about 1/3 that of developing adolescents (P = .0006). TSH levels do not differ significantly between arrested and developing adolescents. These data complement other endocrine data showing significantly lower levels of sex steroids and luteinizing hormone (LH) in arrested males than developing males [Maggioncalda, 1995a,b; Maggioncalda et al., 1999]. Together with documented behavioral differences between reproductive males with and without secondary sexual features, these endocrine data support the hypothesis that in male orangutans there are alternative developmental pathways and corresponding alternative reproductive strategies.


Growth Hormone/urine , Pongo pygmaeus/growth & development , Thyrotropin/urine , Age Factors , Animals , Creatinine/urine , Male , Pongo pygmaeus/physiology , Radioimmunoassay/veterinary , Sexual Maturation/physiology
14.
Am J Phys Anthropol ; 109(1): 19-32, 1999 May.
Article En | MEDLINE | ID: mdl-10342462

For many years researchers have described some male orangutans as "subadult." These males are of adolescent to adult age and are reproductive, but have little to no secondary sexual trait development. Until now the only endocrine study of this arrest of secondary sexual trait development was performed by Kingsley (1982, 1988). She found that "subadult" or arrested males have lower testosterone levels than similar age developing adolescents or adult males. In this study, urine samples were collected over a two-year period from 23 captive male orangutans in order to more fully define male endocrine profiles. Three study males were juveniles, seven were arrested adolescents, six were developing adolescents, and seven were mature adults. Morning samples were analyzed by radioimmunoassay for levels of testicular steroids and gonadotropins and group hormone profiles were compared by analysis of variance. Results illustrate that arrested adolescent orangutans have significantly lower testosterone and dihydrotestosterone (DHT) levels than developing adolescents, but significantly higher levels than juveniles. Luteinizing hormone (LH) levels also differed between arrested and developing adolescents, with arrested males having lower levels. However, follicle stimulating hormone (FSH) levels were similar in both morphs of adolescent male. The overall hormone profiles for arrested and developing adolescent male orangutans suggest that arrested males lack levels of LH, testosterone, and DHT necessary for development of secondary sexual traits. However, they have sufficient testicular steroids, LH, and FSH to fully develop primary sexual function and fertility. These endocrine data help define alternative developmental pathways in male orangutans. The authors discuss the relationship between these developmental pathways and male orangutan reproductive strategies, and hypothesize about their prepubertal socioendocrine determination.


Fertility , Follicle Stimulating Hormone/analysis , Luteinizing Hormone/analysis , Pongo pygmaeus/growth & development , Sex Characteristics , Animals , Animals, Zoo , Circadian Rhythm , Male , Pongo pygmaeus/physiology
15.
J Hum Evol ; 35(4-5): 449-62, 1998.
Article En | MEDLINE | ID: mdl-9774505

Cusps of three second permanent molar teeth belonging to Pan, Pongo and Homo respectively, were chosen where enamel cross striations were easily observed and measured using polarizing light microscopy. Prisms were tracked outwards on photomontages from the dentine horn to the surface of the tooth just lateral to the central gnarled enamel over the cusp tip. Approximately monthly zones of enamel formation were identified and mean cross striation spacings calculated for each zone within each of the three cusps and for the whole of each cusp in total. Enamel secretion rates ranged from 2.5 to 6.5 microns per day with an overall mean value in Pan and Homo of 4 microns per day and of 4.4 microns per day in Pongo for the cuspal enamel. Two of these cusps (of Pan and Pongo) and another of a third permanent molar of Homo were selected for further analysis. Four methods were employed to estimate cuspal enamel formation time. (i) Total counts of enamel cross striations were made through the lateral cuspal enamel on photomontages. The points in the dentine and at the enamel dentine junction (EDJ) corresponding to the end of cuspal enamel formation were defined using incremental and accentuated markings. (ii) Measurements of the average daily rates of dentine formation in each cusp were divided by the length of the axial cuspal dentine formed to give the time of cuspal dentine formation. (iii) A cumulative prism length was calculated close to the EDJ to the end of cuspal enamel formation and divided by the mean cross striation repeat interval along the EDJ to give an estimate of cuspal enamel formation time. (iv) A cumulative time for cuspal enamel formation along the EDJ was calculated by summing successive extension rates for known lengths of the EDJ. This was computed using the formula derived by Shellis (Archs. oral Biol. 29: 697-705, 1984) based on the average daily rate of enamel secretion, the angle of the prisms to the EDJ and the angle of the incremental lines to the EDJ. Each of these methods gave results to within 5% or 10% of a average value for cuspal enamel formation time derived for each cusp. There was no clear indication of additional enamel decussation in any of the cusps studied beyond that recorded in the total counts of cross striations as the prisms were tracked in two dimensions through the lateral cuspal enamel. The results of this study suggest that any one of the methods outlined here may give equivalent estimates of cuspal enamel formation if suitable incremental markings exist in the region being studied.


Dental Enamel/growth & development , Hominidae/growth & development , Pan troglodytes/growth & development , Pongo pygmaeus/growth & development , Tooth/growth & development , Animals , Biological Evolution , Child , Child, Preschool , Dental Enamel/cytology , Dentin/cytology , Dentin/growth & development , Humans , Infant , Infant, Newborn , Species Specificity , Tooth/cytology
16.
Am J Phys Anthropol ; 99(1): 191-203, 1996 Jan.
Article En | MEDLINE | ID: mdl-8928720

This study examines the appearance of the secondary ossification centers in the lower arms, wrists, lower legs, and ankles of a cross-sectional sample of 20 infant orangutans and chimpanzees (15 of known age). The number of tarsal and carpal centers is analyzed relative to the degree of M1 development and the weight of individual animals. Variation in the appearance of these ossification centers is discussed relative to these variables and others. In addition, a sequence of appearance is established for the carpal and tarsal ossification centers in the orangutan and data is presented on the status of these centers in a fetal and newborn gorilla. Study results indicate that 1) there is variation in the number of secondary epiphyses present in animals of similar ages; 2) tarsal ossification is completed prior to carpal ossification in the orangutan; 3) there are indications of a relationship between weight and the number of ossification centers present in animals of similar age; and 4) there appears to be no evidence of specific relationships between carpal and tarsal development and M1 development.


Arm/growth & development , Bone Development/physiology , Carpus, Animal/growth & development , Leg/growth & development , Pan troglodytes/growth & development , Pongo pygmaeus/growth & development , Tarsus, Animal/growth & development , Tooth/growth & development , Animals , Animals, Newborn/growth & development , Animals, Newborn/physiology , Carpal Bones/diagnostic imaging , Carpal Bones/growth & development , Female , Hominidae/embryology , Hominidae/growth & development , Humans , Male , Pan troglodytes/embryology , Pongo pygmaeus/embryology , Radiography , Tarsal Bones/diagnostic imaging , Tarsal Bones/growth & development
17.
Am J Phys Anthropol ; 99(1): 205-20, 1996 Jan.
Article En | MEDLINE | ID: mdl-8928721

This study examines dental formation and alveolar emergence in a large cross-sectional sample composed primarily of wild-reared orangutans (N = 89) in order to provide information on the development of the permanent dentition in this hominoid and to address questions of variation in individual tooth formation, between teeth and between individuals. All specimens have been radiographed in lateral aspect and stages of crown and root formation recorded for all teeth. The ranges of crown and root formation of I1(1), C1(1), P4(4), M2(2), and M3(3) have been calculated relative to the stage of M1(1) development within a specific tooth quadrant. Then, for each specimen, BMDP scatterplot and nonparametric statistics have been used to graph changes in stages of these teeth relative to M1(1) stages and to examine relationships between pairs of upper and lower dental counterparts and between teeth of each jaw. Results indicate 1) high correlations between upper and lower tooth pairs and between many of the permanent teeth within individuals, 2) a relatively large range of variability in individual tooth development (multistage ranges relative to M1(1)), 3) greater variation in root development at emergence than earlier reports, and 4) evidence of variability within the sequence emergence pattern of the orangutan.


Models, Biological , Pongo pygmaeus/growth & development , Tooth/growth & development , Animals , Cross-Sectional Studies , Hominidae/growth & development , Humans , Incisor/diagnostic imaging , Incisor/growth & development , Molar/diagnostic imaging , Molar/growth & development , Morphogenesis , Radiography , Tooth/diagnostic imaging
18.
Am J Phys Anthropol ; 94(4): 499-522, 1994 Aug.
Article En | MEDLINE | ID: mdl-7977677

This study assesses ontogenetic correlates of diet in anthropoid primates. Associations between body weight growth, adult size, and diet are evaluated for a sample of 42 primate species, of which 8 are classifiable as "folivores." The hypothesis that folivores show a pattern of growth that differs from "nonfolivores" is tested. Ontogenetic variation is summarized through use of parametric and nonparametric regression analysis. Several analytical techniques, including broad interspecific and detailed comparisons among species of similar adult size, are applied. This investigation indicates a clear association between body weight ontogeny and diet: folivorous species grow more rapidly over a shorter duration than comprably sized nonfolivorus species. A positive correlation between adult size and diet is not unambiguously established in this sample. A threshold (at around 1 kg) below which insectivory is very common may adequately characterize the association between adult size and diet in anthropoid primates. Above this threshold, adult size does not appear to covary predictably with diet. Evolutionary correlates of the ontogenetic pattern seen in folivores may include a variety of factors. The distinctive pattern of development in folivores may relate to the profile of ecological and social risks that these species face. Morphophysiological advantages to rapid growth may relate to a need for accelerated alimentary (dental and gut) development. The implications of ontogenetic variation in folivores are discussed.


Body Weight/physiology , Diet , Haplorhini/growth & development , Age Factors , Alouatta/growth & development , Animals , Biological Evolution , Body Constitution , Cercopithecidae/growth & development , Dietary Fiber/administration & dosage , Female , Gorilla gorilla/growth & development , Hylobates/growth & development , Macaca/growth & development , Male , Pan troglodytes/growth & development , Papio/growth & development , Plants , Pongo pygmaeus/growth & development
19.
Am J Phys Anthropol ; 90(2): 229-36, 1993 Feb.
Article En | MEDLINE | ID: mdl-8430755

Few data are available for assessing the relative testicle size of orang-utans, Pongo pygmaeus, so measures were obtained for 31 individuals of varying age. It was shown that the volume of the testicles, calculated from in situ measures of testicle length and breadth, closely approximates testicle weight when multiplied by the specific gravity of solid tissue. Growth curves for body weight and data published for wild specimens were evaluated to obtain the weight most characteristic of male Pongo, and the ratio of testicle weight to body weight was calculated. The mean ratio for individuals with fully adult stature is 0.034, similar to but smaller than that of humans at about 0.050, and larger than the ratios reported for 5 gorillas at 0.013. The testicles mature faster than the body, however, so the mean ratio for young adult orang-utans is about 0.056 and resembles the ratio for humans more closely than the full adults. The differences between the ratios for a monogamous gibbon species, orang-utans, and humans is accounted for when testicle size relative to the weight of the female is considered. This is consistent with a sperm dilution effect produced by variation in the size of the female reproductive tract. The small relative testicle size of the gorilla is anomalous and requires verification as does the application of female size to scale the testicles.


Body Constitution/physiology , Pongo pygmaeus/anatomy & histology , Testis/anatomy & histology , Animals , Body Weight , Male , Organ Size , Pongo pygmaeus/growth & development , Testis/growth & development
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