Femur/stature ratio and estimates of stature in mid- and late-Pleistocene fossil hominids

In previous limited investigations of the human femur/stature ratio we (Feldesman and Lundy: Journal of Human Evolution 17:583-596, 1988; Feldesman et al.: American Journal of Physical Anthropology 79:219-220, 1989) have shown it to be remarkably stable across ethnic and gender boundaries. In this study we evaluate the femur/stature ratio in 51 different "populations" of contemporary humans (n = 13,149) sampled from all over the world. We find that the mean ratio of femur length to stature in these populations is 26.74%, with a very restricted range of variation. When we compare mean femur/stature ratios of males and females, there are no statistically significant differences. ANOVA performed on a naive grouping of samples into "whites," "blacks," and "Asians" indicates that there are significant racial differences (P less than 0.001). When we subject these groups to Tukey's HSD procedure (a post-hoc test), we find that "blacks" are responsible for the significant ANOVA, being significantly (P less than 0.005) different from the other ethnic groups. "Whites" and "Asians" are not significantly different (P = 0.067) under the conditions of this analysis, although all these racial comparisons may be suspect given the small sample sizes. We tested the efficacy of the ratio in three situations: predicting stature of repatriated white Vietnam veterans; predicting stature in a random sample of South African blacks (of known stature), and predicting the stature of a single Akka pygmy. In the first and third cases, the femur/stature ratio does better than the traditionally recommended regression equation, while in the second case the predictions from the femur/stature ratio are less accurate than from the appropriate regression equation. These results encouraged us to apply this ratio to mid- and late-Pleistocene fossil hominids, where the choice of reference population for stature estimates continues to trouble workers. We estimated stature for a sizeable number of Homo erectus (HE), early Neanderthal (EN), Near Eastern Neanderthal (NEN), and early anatomically modern Homo sapiens (EAMHS) by using the simple relationship: stature (cm) = femur length (cm) * 100/26.74. Our results show that HE fossils are slightly taller on average than either EN or NEN samples, which do not differ significantly in stature, while EAMHS fossils are significantly taller than all three earlier groups. While these results are not surprising, our stature estimates for these fossils differ from currently published estimates based on sample-specific regression-based formulae.(ABSTRACT TRUNCATED AT 400 WORDS)     

Trends in stature in the South Australian Aboriginal Murraylands

Millennial and secular changes in body height of prehistoric and recent Aboriginal South Australians are investigated. Skeletal remains of 55 male and 40 female individuals who were excavated at Roonka on the River Murray were dated from 9800 to 100 years BP. Stature was reconstructed by using humerus, femur, and tibia ratios to stature derived from Abbie's (1975) data on living Aborigines and the Trotter-Gleser method for blacks. The respective averages were 1,652 mm and 1,665 mm for males and 1,527 mm and 1,549 mm for females. In 1996/1997, statures of 27 adult males and 21 adult females were measured in Aboriginal centers of Gerard and Raukkan (Point McLeay) on the Lower River Murray. These people, as far as it can be ascertained, are the descendants of the people from Roonka. Their statures were adjusted for the stature loss with age, so that the data represent young individuals (≤30 years of age). The average male stature was 1,712 mm, and the average female stature was 1,567 mm. Data collected by Wood Jones and Campbell in 1924 for Aboriginal South Australians show that young adult male stature was 1,668 mm (n = 6), and female stature was 1,552 mm (n = 4). Slopes of regressions of individual statures on radiocarbon dates and on dates of birth are not significantly different from zero. The same is true for regressions of individual long bone lengths on radiocarbon dates. It can be concluded that there was little change in stature of Aboriginal South Australians from prehistoric to recent times. Regressions of individual age-corrected heights on birth dates (1860–1980) of Aboriginal men and women measured in 1924 and in 1996 further indicate no significant increase in height in either sex. Am J Phys Anthropol 106:505–514, 1998. © 1998 Wiley-Liss, Inc.     

Relation between fat mass, fat free mass and ventilatory function in children and adolescents

The aim of the present study was to evaluate the relation between fat mass (FM), fat free mass (FFM) and ventilatory function in children and adolescents. 1 174 healthy children and adolescents (583 males and 591 females) aged 10-18 years were selected from Heilongjiang Province through random sampling by means of questionnaire and physical examination, and measured for height, weight, waist to hip ratio (WHR), FM, FFM and ventilatory function. The data were analyzed by means of independent-samples t test, Pearson correlation analysis and multi-factors regression analysis. Regardless of sex, an independent positive correlation was found (P<0.001) between age and FFM index (FFMI). FM index (FMI) correlated negatively with age in males (P<0.001), but positively with age in females (P<0.001). Regardless of sex, FFMI correlated positively with forced vital capacity (FVC), forced expiratory volume in one second (FEV1), peak expiratory flow (PEF), forced expiratory flow at 25% of forced vital capacity (FEF25%), FEF50%, and maximal mid-expiratory flow (MMEF) (P<0.05), while negatively with FEV1/FVC (P<0.01). FFMI was correlated positively with FEF75% in males (P<0.05), but not correlated in females. In males, FMI correlated negatively with FEV1, FEV1/FVC, PEF, FEF25%, FEF50%, FEF75% and MMEF (P<0.05), but not correlated with FVC. No correlation was found between the ventilatory function indices and FMI in females. Except FEV1/FVC and FEF75% in males, the effect of FFMI in predicting ventilatory function was higher than FMI regardless of sex. Moreover, the predicting effect of FFMI was higher in males than that in females. Growth spurt of lung function occurred in the ages of 12-15 years in males, while in the ages of 12, 13 and 18 years in females. During the period of growth spurt of lung function, regardless of sex, the effect of FFMI in predicting the lung function was higher than that of age. In conclusion, regardless of sex, FFMI correlates positively with ventilatory function, as a reflection of muscle mass. The effect of FFM in predicting ventilatory function is higher in males than that in females. FM correlates negatively with ventilatory function in males, but not in females. The rapid growth of height and FFM are possibly the main reasons for growth spurt of lung function.     

Longitudinal analysis of length growth in the chimpanzee (Pan troglodytes)

The adolescent growth spurt in linear dimension in humans is considered to be unique among mammals, but few comparative studies have been done, even on chimpanzees. Growth of the summed length of crown to rump, thigh, and leg was studied longitudinally in 12 chimpanzees. We took body weight growth and reproductive maturation into consideration. Reproductive maturation was monitored by the swelling of sexual skin and menarche in females, and by testicular development in males. We applied two relationships found in humans between body length growth and the environment to the chimpanzees. The first relationship was the robustness of the growth spurt, meaning that the spurt is absent only in individuals under the most severe environmental pressure. Subjects maturing in a favorable or even mediocre environment are anticipated to show the growth spurt. The second relationship was catch-up growth, where, when the environment is ameliorated, growth may be accelerated to attain the target size. Catch-up growth at the end of the juvenile period may mimic the adolescent growth spurt. Results showed that subjects living under favorable conditions did not exhibit a growth spurt, and that it was only the subjects who had delayed growth in the juvenile period that showed a spurt in adolescence, the period when reproductive maturation occurred. Although we have concluded that chimpanzees do not have an adolescent growth spurt, except in cases of catch-up growth, this does not mean that they have a different growth pattern from that of humans. The absence of a growth spurt may be associated with adaptations to chimpanzee patrilineal society, where adolescent males are incorporated into the adult hierarchy at a low rank.     

Growth standards for the tibia and radius in children aged one month through eighteen years

Standards for the growth of the tibia and the radius are presented for normal males and females ages one month through 18 years. Using radiographs of subjects from the Fels Research Institute for the Study of Human Development longitudinal program, means and standard deviations for bone length, interval increments and annual increments were determined. Males and females show little difference in growth of the tibia until adolescence while statistically significant differences are found at nearly all ages in the radius. The adolescent growth spurt occurs in the male from 12–15 years and in the female from 9–12 years.     

Just how strapping was KNM-WT 15000?

For over twenty years, the young, male Homo erectus specimen KNM-WT 15000 has been the focus of studies on growth and development, locomotion, size, sexual dimorphism, skeletal morphology, and encephalization, often serving as the standard for his species. Prior research on KNM-WT 15000 operates under the assumption that H. erectus experienced a modern human life history, including an adolescent growth spurt. However, recent fossil discoveries, improvements in research methods, and new insights into modern human ontogeny suggest that this may not have been the case. In this study, we examine alternative life history trajectories in H. erectus to re-evaluate adult stature estimates for KNM-WT 15000. We constructed a series of hypothetical growth curves by modifying known human and chimpanzee curves, calculating intermediate growth velocities, and shifting the age of onset and completion of growth in stature. We recalculated adult stature for KNM-WT 15000 by increasing stature at death by the percentage of growth remaining in each curve. The curve that most closely matches the life history events experienced by KNM-WT 15000 prior to death indicates that growth in this specimen would have been completed by 12.3 years of age. These results suggest that KNM-WT 15000 would have experienced a growth spurt that had a lower peak velocity and shorter duration than the adolescent growth spurt in modern humans. As a result, it is likely that KNM-WT 15000 would have only attained an adult stature of 163 cm (∼5′4″), not 185 cm (∼6′1″) as previously reported. KNM-WT 15000's smaller stature has important implications for evolutionary scenarios involving early genus Homo.     

The effects of aging and secular trend on adult stature in rural western Ireland

Cross-sectional data, consisting of anthropometric measurements for 347 adult males and 261 adult females in western Ireland measured during the 1930s, were used to determine the effects of aging and secular change upon stature. Estimates of statural loss due to aging were obtained using partial regression of stature on age while controlling for subischial length, and regression of the difference between observed stature and maximum predicted stature on age. Males show the effects of aging to a greater extent than do females. After correction for the effects of aging, the adjusted values of stature were regressed on age to estimate secular trend of stature. For males, there is a general increase of stature with time, excepting those born around 1878, while females generally show random variation with time. Both male and female adjusted stature decrease sharply around 1878, for which alternative historical explanations are proposed, relating to differential migration and survival.     

Parent-child correlation for various indices of adiposity in an endogamous Indian population

The study was conducted on 1,042 Punjabi adults and adolescent boys and girls (11-17 years) belonging to middle class families residing in Delhi, India. To study the relative influence of genetic and environmental factors on various fat measures, a set of 7 body measurements namely weight, stature and skinfold thickness at biceps, triceps, subscapular, suprailiac and medial calf measurements was taken on each subject. There was a redistribution of fat away from extremity towards the trunk, a rapid occurring process in males than in females. Increase in body mass index (BMI) with age was more pronounced in females than in males, both at adolescence and adult stage. There was an increase in grand mean thickness (GMT) calculated as mean of all five skinfold thicknesses, in adolescent girls where as in adolescent boys it fluctuated with age. The trunk/extremity ratios reflected a trend in favor of increase in trunk fat, more marked in boys than in girls. The correlations were of low magnitude, however, some skin folds displayed relatively higher value of correlation indicating that these could be determinant of adult obesity.     

Pubertal timing, hormones, and body composition among adolescent Turkana males

The Turkana, like other East African pastoral groups, are known for their tall adult stature, achieved despite a blunted growth spurt during adolescence and continued growth into the early 20s. To investigate the hormonal mechanisms associated with the pattern of slow and continued adolescent growth, we collected data on hormonal status, height, weight, and trunk skinfolds and ethnographic self-reports of testicular maturation in a cross-sectional sample of 35 nomadic and 37 settled Turkana males aged 14-24. Hormonal determinations included testosterone (T), sex hormone-binding globulin (SHBG), and dehydroepiandrosterone (DHEA) in blood, in addition to urinary DHEA. Self-reports of testicular maturation showed no difference between settled and nomadic subpopulations. However, nomadic boys exhibited significantly higher levels of T, DHEA, and SHBG. Of all the hormones, only SHBG showed a significant relationship with age. Multiple regression models show blood T and SHBG to be significant independent predictors of achieved height as well as weight, controlling for age. Our results suggest that onset of puberty is substantially delayed among Turkana males, and that bioavailable T is related to growth in stature during adolescence. We suggest that SHBG acts to mediate the effects of energy availability on adolescent growth in this energetically limited population. Our findings may also have implications for understanding adolescent growth among Homo erectus.     

Application of the anatomical method to estimate the maximum adult stature and the age‐at‐death stature

This study focuses on the age adjustment of statures estimated with the anatomical method. The research material includes 127 individuals from the Terry Collection. The cadaveric stature (CSTA)–skeletal height (SKH) ratios indicate that stature loss with age commences before SKH reduction. Testing three equations to estimate CSTA at the age at death and CSTA corrected to maximum stature from SKH indicates that the age correction of stature should reflect the pattern of age‐related stature loss to minimize estimation error. An equation that includes a continuous and linear age correction through the entire adult age range [Eq. (1)] results in curvilinear stature estimation error. This curvilinear stature estimation error can be largely avoided by applying a second linear equation [Eq. (2)] to only individuals older than 40 years. Our third equation [Eq. (3)], based on younger individuals who have not lost stature, can be used to estimate maximum stature. This equation can also be applied to individuals of unknown or highly uncertain age, because it provides reasonably accurate estimates until about 60/70 years at least for males. Am J Phys Anthropol 152:96–106, 2013. © 2013 Wiley Periodicals, Inc.     

The short die young: the interrelationship between stature and longevity-evidence from skeletal remains

It has long been observed that tall people display longer life spans. The current data were employed to verify this association within the bioarchaeological context. To this end, stature and its association with age-at-death were analyzed in a pooled sample of 2,923 skeletons. Height was estimated from proxy indicators based on the maximum length of the humerus, radius, femur, and tibia. Stature estimation followed the procedure outlined by Pearson ([1899] Philos. Trans. R. Soc. Lond. [A] 192:169-244), incorporating minor modifications by R?sing ([ 1988] Handbuch der vergleichenden Biologie des Menschen; Stuttgart: Gustave Fischer, p 586-600). Individual age estimates were classified into three mutually exclusive age groups: 20-39 years (591 males, 667 females), 40-59 years (876 males, 499 females), and 60+ years (171 males, 119 females). The results document that both sexes display a statistically significant inverse relationship between adult height and age-at-death (males, P < 0.01; females, P < 0.05). Taking an epidemiological approach, the risk model implies that the estimated odds of survival beyond age 40 improve by approximately 16% for 1 SD in bone length. However, not all bones may be equally adept at displaying the association. The radius failed to support the positive association between stature and longevity, which may be indicative of a relatively greater contribution of environmental factor to radius length. Overall, the relationship between body height and longevity is not causal but coincidental: mitigated by diverse environmental factors such as nutrition, socioeconomic stressors, and disease load.     

达斡尔族中小学生体质发育现状及20多年来的变化

本文报道了6~18岁1993名达斡尔族学生8项体质指标(身高、坐高、体重、肩宽、骨盆宽、胸围、腰围和臀围)的测量结果,并计算了10项体质指数。结果发现,达斡尔族在我国属体质发育较高的民族,并表现为一定的城乡差异;20多年来达斡尔族学生身高、体重、胸围全面增长,男女生身高最大增长年龄均提前约1岁左右,男生高年龄组身高和身体充实度增幅较大,但女生变化不大且肩宽和骨盆宽呈下降趋势。提示达斡尔族青少年体质发育表现为以生长突增提前为主的生长长期趋势,但女生高年龄组身高增长不明显、身体充实度有待提高,应采取营养和锻炼等措施促进其生长发育水平全面提高。     

Aging changes in the medullary cavity of the proximal femur in American Blacks and Whites.

This study explores changes with age in the medullary cavity in an area of the femur which is becoming of increasing clinical interest. It is based on measurements of medial-lateral and posterior-anterior radiographs of the proximal one-third of the right femur, below the greater trochanter. The study population consisted of 257 individuals from the Terry collection in the Smithsonian Institution and included Blacks and Whites, males and females, aged 20 to 90 years. Medullary cavity and external diameters were measured at 11 levels, beginning with a line drawn perpendicular to the linea aspera at the level of the inferior border of the greater trochanter. To correct for size differences, the interval between levels was set at one-fourth the individual femoral head diameter. The data were subjected to regression analysis and analysis of variance. Anterior-posterior medullary diameter is more highly correlated with age than medial-lateral diameter. Females show the greatest relative increase with age in both dimensions, especially at subtrochanteric levels, and they tend to have relatively larger medullary cavities than males at all ages. White males have relatively larger medullary diameters than Black males. Younger White females have relatively larger medullary cavities than Black females, but the latter reach parity with White females in middle age and show a greater overall percentage of medullary expansion.     

Adult stature and age at menarche in Zapotec-speaking communities in the Valley of Oaxaca,Mexico, in a secular perspective

Adult stature and the age at menarche among individuals from Zapotec-speaking communities in the Valley of Oaxaca in southern Mexico are considered in a secular perspective. Four sets of observations are utilized: (1) adult stature in males and females from five rural communities; (2) age at menarche in adult women and school girls from a single rural community; (3) earlier studies of adult stature in the Valley of Oaxaca; and (4) estimated stature from long bones excavated in various archaeological sites in the Valley of Oaxaca. There were no significant differences among the five communities for stature; hence, the data were pooled for analysis and comparison. Results of linear regression of stature and stature adjusted for the estimated effects of aging after 30 years of age on year of birth indicate negligible secular changes in either sex. Comparisons with statures from earlier surveys, the earliest dates to 1899, also indicate negligible changes. When adult women are grouped according to age, there are no differences in mean ages at menarche between the older and younger women. Mean age at menarche for the total adult sample is 14.53 ± 0.08 years, which compares favorably with the probit estimate for school girls, 14.70 ± 0.32 years. These results thus suggest virtually no secular change in adult size and maturity of the Zapotec-speaking population in the Valley of Oaxaca over the past 80 years. Differences in stature between contemporary populations and estimated statures from long bones from several archaeological sites in Oaxaca are small, and thus suggests little secular change over the past one to two–thousand years.     

Pubertal origin of the larger sex dimorphism for adult stature of a Chilean population

Students aged 6 to 20 years attending the public schools in the Northern Area of Santiago, Chile, were examined to search for the developmental origin of the large sex dimorphism in adult stature found in this population. Stature, biacromial diameter, and signs of sexual maturation were studied and comparisons were made with European samples. All of the variables showed that Chilean females reach puberty earlier than, and cease growth before Europeans, while males mature at the same pace as Europeans. It is concluded that the large sex dimorphism in adult stature found in this sample is mainly due to this earlier cessation of growth in Chilean females.     

青海藏族青少年骨龄与生长发育关系研究

本文报告了青海省境内,世居在海拔3000-4000米地区的728名7-18岁健康藏族青少年学生的手、腕部骨骼发育情况,对骨化中心出现和骨骺愈合求出了50%出现年龄,并对骨龄与青春期身高突增的关系及与月经初衬潮的关系进行了分析。     

Sexual dimorphism in the growth of the cranium

The major sexual dimorphisms in body size appear at puberty but, by then, 95% of the growth of the cranium is completed. As sexual dimorphism in the cranium is as great as for other parts of the body, this suggests that it must appear at an earlier age, and that cranium/body size ratios for the two sexes will vary during growth. Results from a longitudinal study of Montreal children are used to investigate this phenomenon. The effect is expressed quantitatively by proportional growth and growth velocity curves, based on the final size of boys, which show that the dimorphism indeed makes an early appearance. The data are also analyzed on an age scale relative to the ages of peak growth velocity in stature, derived from the individual growth curves. This shows that although there is a minor pubertal spurt in growth for the external cranial dimensions of boys, it contributes relatively little to the final dimorphism in cranial size. To summarize this aspect of growth, an index of cephalization is calculated: head length × head width/stature. Cross-sectional standards for the change of the mean index with age show a linear decline for boys and girls until puberty, with a constant difference between them. After puberty, the index becomes equal in the two sexes. Individual development curves for the index are however not linear.     

The growth pattern of chimpanzees: Somatic growth and reproductive maturation inPan troglodytes

Growth of chimpanzees reared at the Kumamoto Primates Park of Sanwa Kagaku Kenkyusho Co. Ltd. was studied cross-sectionally from the viewpoints of somatic growth and reproductive maturation. Distance and velocity curves were expressed using spline function method. Males showed adolescent growth acceleration in body weight, with a peak at 7.86 yrs of age, but not in trunk length. Females showed continuous rapid growth from mid-juvenile to adolescent phase in both body weight and trunk length, but no isolated adolescent spurt. The Sanwa chimpanzees matured at about 12.5 yrs of age for females and 15.0 yrs for males. The mean adult weights and trunk lengths were 53.2 kg and 507.8 mm for males and 42.7 kg and 481.6 mm for females. The Sanwa chimpanzees had similar growth patterns to those of the Yerkes chimpanzees, although they showed a slight delay in infancy, and a higher growth rate from the early juvenile phase onwards. Growth patterns in these two laboratories may be regarded as “normative” for laboratory-reared chimpanzees. They matured earlier than wild chimpanzees by more than two years. The major reason for the retarded maturation in wild chimpanzees is the delay of growth from infant to the early juvenile phases (0–4 yrs of age), probably owing to a limited nutritional supply from the mother. Development of the testes comprised three phases: slow growth from infant to juvenile (until 6.4 yrs); rapid growth around adolescence (until 9.2 yrs); and adult (mean testicular volume, 187 cm³). Setting the nutritional standard at 2,000–2,600 Cal/day (= Kcal/day) per adult, calories were considered for captive chimpanzees in each age class.     

Gender-specific growth patterns for stature,sitting height and limbs length in Croatian children and youth (3 to 18 years of age)

In a cross-sectional study of growth, 5,155 children (2,591 females, 2,564 males) from the town of Zagreb (Croatia) were measured. Four traits of linear dimensionality (stature, sitting height, arm and leg lengths) were studied in the age span of 3 to 18 years. A significant average annual increase of all four anthropometric parameters were observed up to 14 and 15 years of age in girls and 16 years of age in boys, showing that girls had a shorter growing period. In the prepubertal period until 9 years of age, gender differences were negligible. At the age of 10, boys were overgrown by girls in all parameters due to the earlier onset of puberty in girls. The growth gains for girls, when compared with those for boys, show a different pattern across variables. The female growth advantage remained in a two years period for the limbs length, but in a three year period for stature and the longest, for 4 years, for sitting height. The male predominance in size had an onset at the age of 13 for the limbs and in the age of 14 for stature and sitting height. The patterns of sexual dimorphism in stature and sitting height during growing years are similar to those observed in other populations of Europe. Growth of Croatian children and youth is very similar to that of the tallest European populations.