掌骨X线测量推断身高的研究

随机选取在校健康大学生186人(男90人, 女96人, 年龄18—27岁), 拍摄双手后前位372侧X线片, 测量身高和掌骨的长与宽。通过掌骨和身高的测量, 分析掌骨各参数与身高的关系, 为人类学和法医学的身高推断积累研究资料。掌骨长与身高的相关性明显高于掌骨宽, 其中男性第2掌骨长与身高相关性最高, 其线性回归方程为Ym=1097.320+9.337X; 女性第3掌骨长与身高的相关性最高, 其线性回归方程为Yf=1016.752+9.878X。男性第2掌骨长和女性第3掌骨长与身高的相关性最高, 可分别作为推断身高的依据。     

Skeletal maturity and bone growth in twins

Heritability of skeletal maturity and bone growth is discussed on the basis of intrapair resemblances (correlation coefficients) and differences (revised percent deviations) in mono- and dizygotic twins and random pairs of unrelated children. A series of 1072 radiographs of the right hand and wrist in 63 male and 70 female pairs of monozygotic twins, and 25 male and 21 female pairs of dizygotic twins aged 12 to 18 years studied longitudinally in Tokyo were used. Skeletal maturity based on the TW2 age suggests higher heritability than bone growth based on the second metacarpal dimensions. In the latter, length has higher heritability than width and cortical thickness. A dosage effect seems to be suggested in width and some indices in the second metacarpal, but is not confirmed in skeletal maturation.     

Using scapular measurements in regression formulae for the estimation of stature

There are very few papers in forensic literature in which scapular dimensions have been used for estimation of living stature. Allowing the forensic duty to estimate the living stature of skeletal remains, using intact or fragmented scapulae, the Authors have performed multiple regression analysis between the measurements taken from 80 scapula (40 male and 40 female) belonging to a skeletal collection with anthropometric known data. Seven parameters (max length, max breadth, max acrocoracoid distance, length of acromion, max length of coracoid, length of glenoid cavity, width of glenoid cavity) have been recorded. By statistical analysis multiple and linear regressions have been obtained. The results show that living stature may be determined by using regression formulae of single or associated parameters taken from whole or fragmented scapulae. In absence of intact or fragmented long limb bones, scapula sample can be reliably employed for the estimation of stature in forensic practice.     

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.     

A combined morphometric analysis of foot form and its association with sex,stature, and body mass

Objectives: Morphometric analysis of footprints is a classic means for orthopedic diagnosis. In forensics and physical anthropology, it is commonly used for the estimation of stature and body mass. We studied individual variation and sexual dimorphism of foot dimensions and footprint shape by a combination of classic foot measurements and geometric morphometric methods. Methods: Left and right feet of 134 healthy adult males and females were scanned twice with a 3D optical laser scanner, and stature as well as body mass were recorded. Foot length and width were measured on the 3D scans. The 2D footprints were extracted as the plantar‐most 2 mm of the 3D scans and measured with 85 landmarks and semilandmarks. Results: Both foot size and footprint shape are sexually dimorphic and relate to stature and body mass. While dimorphism in foot length largely results from dimorphism in stature, dimorphism in footprint shape partly owes to the dimorphism in BMI. Stature could be estimated well based on foot length (R² = 0.76), whereas body mass was more closely related to foot width (R² = 0.62). Sex could be estimated correctly for 95% of the individuals based on a combination of foot width and length. Discussion: Geometric morphometrics proved to be an effective tool for the detailed analysis of footprint shape. However, for the estimation of stature, body mass, and sex, shape variables did not considerably improve estimates based on foot length and width. Am J Phys Anthropol 157:582–591, 2015. © 2015 Wiley Periodicals, Inc.     

Maturity Ogives for South Pacific Albacore Tuna (Thunnus alalunga) That Account for Spatial and Seasonal Variation in the Distributions of Mature and Immature Fish

Length and age at maturity are important life history parameters for estimating spawning stock biomass and reproductive potential of fish stocks. Bias in estimates of size and age at maturity can arise when disparate distributions of mature and immature fish within a population are not accounted for in the analysis. Here we investigate the spatial and temporal variability in observed size and age at maturity of female albacore tuna, Thunnus alalunga, using samples collected across the South Pacific. Maturity status was identified using consistent histological criteria that were precise enough to allow for mature but regenerating females to be distinguished from immature females during the non-spawning season, permitting year-round sampling for maturity estimation in albacore. Using generalised linear mixed models, we found that the proportion of mature females at length varied significantly with latitude and time of year. Specifically, females at northern latitudes (∼10–20°S, where spawning occurs) were mature at significantly smaller lengths and ages than females at southern latitudes (∼20–40°S), particularly during the spawning season (October–March). This variation was due to different geographic distributions of mature and immature fish during the year. We present a method for estimating an unbiased maturity ogive that takes into account the latitudinal variation in proportion mature at length during a given season (spawning or non-spawning). Applying this method to albacore samples from the western region of the South Pacific gave a predicted length at 50% mature of ∼87 cm fork length (4.5 years).     

Body mass and stature estimation based on the first metatarsal in humans

Archaeological assemblages often lack the complete long bones needed to estimate stature and body mass. The most accurate estimates of body mass and stature are produced using femoral head diameter and femur length. Foot bones including the first metatarsal preserve relatively well in a range of archaeological contexts. In this article we present regression equations using the first metatarsal to estimate femoral head diameter, femoral length, and body mass in a diverse human sample. The skeletal sample comprised 87 individuals (Andamanese, Australasians, Africans, Native Americans, and British). Results show that all first metatarsal measurements correlate moderately to highly (r = 0.62-0.91) with femoral head diameter and length. The proximal articular dorsoplantar diameter is the best single measurement to predict both femoral dimensions. Percent standard errors of the estimate are below 5%. Equations using two metatarsal measurements show a small increase in accuracy. Direct estimations of body mass (calculated from measured femoral head diameter using previously published equations) have an error of just over 7%. No direct stature estimation equations were derived due to the varied linear body proportions represented in the sample. The equations were tested on a sample of 35 individuals from Christ Church Spitalfields. Percentage differences in estimated and measured femoral head diameter and length were less than 1%. This study demonstrates that it is feasible to use the first metatarsal in the estimation of body mass and stature. The equations presented here are particularly useful for assemblages where the long bones are either missing or fragmented, and enable estimation of these fundamental population parameters in poorly preserved assemblages.     

Cortical bone loss and measurements of the second metacarpal bone: II. Hypodense bone in postwar Guamanian children

Hand-wrist radiographs from 326 Guamanian children (180 boys and 146 girls) were evaluated for total width, medullary width, length, and combined cortical thickness of the second metacarpal. Bone measurements as well as standing height and weight were compared to similar published data from U.S. mainland black, white, and Mexican-American children. The results demonstrated that the second metacarpal bones of Guamanian boys and girls of all age groups (5–17 years) have a narrower width and shorter length with less combined cortical thickness than any of the other groups. Guamanian children also weighed less and were of shorter stature than their black, white, or Mexican-American counterparts. These results agree closely with those comparisons between Guamanian and U.S. mainland white adults published earlier. It is not possible from the present data to ascertain whether these differences were due to genetic variability or nutritional deficiency.     

From footprint morphometrics to the stature of fossil hominins: A common but uncertain estimate

Hominin footprints are a particular remain in paleoanthropology representing brief moments of life of extinct individuals. Footprints not only provide information on the locomotor behavior of fossil taxa but also on their body characteristics such as their stature. This stature is usually estimated from the length of the footprints based on the well-known foot length to stature ratio. However, footprint length does not result only from the foot length but of a combination of factors. Therefore, it is necessary to investigate the relationships between footprint length and stature of individuals using experimental approaches. Secondly, recent discoveries of fossil footprints have led to the estimation of statures from isolated footprints. However, such estimates may be biased because of the intraindividual morphometric variation of the footprints. Moreover, footprints may also be incomplete making it impossible to measure the length and therefore the estimation of a stature. The search for relationships between stature and other morphometric variables is therefore necessary to have the most accurate picture possible of the individuals who left these tracks. In this context, this article reports the results of an experimental study that aims to determine the relationships between the stature of individuals and different morphometric variables and to quantify the intraindividual variation of each variable. Thus, 21 morphometric variables were measured on a total of 175 experimental footprints left by 20 individuals in an experimental area composed of loose sand. Statistical analyses show that footprint lengths are not only the variables most correlated with stature but also those with the least intraindividual variation. However, estimation of stature from footprints left by fossil hominins is subject to three types of uncertainties: residuals from linear regression, intraindividual variation that can be particularly large in soft substrates, and the application of relationships defined on modern populations to fossil taxa.     

A craniofacial growth maturity gradient for males and females between 4 and 16 years of age

Differential growth of the craniofacial complex implies variation in ontogenetic patterns of development. This investigation quantifies the relative maturity—as defined by percent adult status—of nine cephalometric dimensions and stature. Analysis is based on 663 lateral cephalograms from a mixed longitudinal sample of 26 males and 25 females between 4 and 16 years of age. Graphic comparison of maturity status across the age range shows that variation is intergraded between the neural and somatic growth maturity patterns, as described by head height and stature, respectively. The maturity gradient moves from head height through anterior cranial base, posterior cranial base and maxillary length, upper facial height, corpus length, and ramus height to stature. After 9 years of age ramus height is less mature than stature. Anterior maxillary and mandibular heights diminish during transitional dentition and thereafter exhibit maturity patterns that compare to corpus length. Although females are consistently more mature than males, the gradient of variation between dimensions is sex independent.     

The estimation of adult stature from metacarpal bone length

Stature was measured (in cm) in 166 (120 male; 46 female) predominantly white adults (age range: 17–87 years). A radiograph of one hand of each subject was taken (for routine diagnostic purposes) and the inter-articular length of all five metacarpal bones was measured with a sliding caliper. These metacarpal lengths were then adjusted to compensate for enlargement during radiography. A significant correlation coefficient between stature and metacarpal length was observed in both sexes. Regression equations were computed from the length of each metacarpal, by which living stature may be fairly accurately estimated in the absence of any complete limb bones. The difference between our estimates and those obtained by more orthodox methods is usually less than 3%.     

Morphometric dimensions of metacarpal bones in the population structure analysis (island of Krk, Croatia)

The population structure analysis by means of the osteometric dimensions of metacarpal bones in the population groups of the northern Adriatic island of Krk, Croatia was performed. The sample consisted of randomly sampled adult islanders (94 males and 79 females) aged from 18 to 85 years from six villages of the island of Krk. "Biological distances" were estimated by the Mahalanobis D2 analysis for bone length (L), total diaphysis width (T) and medullary canal width (M) dimensions of the second left metacarpal bone. Analysis of the osteometric dimensions of metacarpal bones as a measure of biological distance between population groups of the island of Krk indicated bio-cultural and socio-cultural events, rather than geographical distances, to be the primary determinants of anthropogenetic structure of today's population groups of the island.     

Fatness and skeletal maturity of Belgian boys 12 through 17 years of age

Relationships between fatness and skeletal maturity are considered in a nationwide sample of 14,259 Belgian boys 12 through 17 years of age (The Leuven Growth Study of Belgian Boys). Absolute fatness was estimated from four skinfolds using the Drinkwater and Ross technique and from the sum of four skinfolds, and was related to skeletal maturity assessed by the Tanner-Whitehouse method (I and II). In addition, comparisons were made between the fattest 5% and leanest 5% of the boys at each age level. Correlations between the indices of fatness and skeletal age and relative skeletal age (the difference between skeletal and chronological ages) are positive and generally low, ranging from 0.12 to 0.39. They tend to decrease with age from 12 to 17 years. Comparisons between the extreme groups indicate that the leanest boys are more delayed in skeletal maturity, by about 0.8 years, than the fattest boys are advanced, by about 0.5 years. Stature data for the same boys are consistent with the skeletal maturity data and thus suggest that the size differences between the extreme groups are due in part to maturity differences. Over the age span 12 through 20 years, the leanest boys are reduced in stature by about – 1.2 standard deviations, while the fattest boys are larger in stature by about +0.6 standard deviation units. The size differences, however, persist after skeletal maturity is attained so that there may be a specific role for fatness in influencing statural growth.     

Estimation of stature from the skeletal reconstruction of an immature Neandertal from Dederiyeh cave, Syria

Skeletal reconstruction of a child Neandertal unearthed at Dederiyeh Cave, Syria in 1993, is undertaken and the acquired stature discussed. Although the skeletal remains were well preserved, the reconstruction required several assumptions to be made because of the immature status of the specimen. The assumptions were mainly concerned with distances between bones in the inter-vertebral spaces and in the joints of the hip, knee, and ankle. These were estimated from X-ray films of modern children and data from previous studies. Stature was directly measured on the reconstruction, and found to be 79.2 cm. After corrections for soft tissue thickness and shrinkage of the casts, the stature became 81.7 cm. This estimate is consistent with estimates based on regression equations of long bone lengths, especially from those of the lower extremity. In comparison with longitudinal data for white American boys, the assessment of stature for Dederiyeh varied according to the estimated age. For a younger estimated age, the stature falls in the lower half of the white American range of variation, but with an older estimated age, it falls below the lower limit of the range of variation. Other immature Neandertals including two European specimens, Roc de Marsal and La Ferrassie 6, fall below the lower limit of the 5th to 95th percentile range based on the estimated statures from their long bone lengths. More comprehensive age assessment covering both fossil and modern humans is required before accurate conclusions in relation to Neandertal growth can be drawn.     

Stature and body mass estimation from skeletal remains in the European Holocene

Techniques that are currently available for estimating stature and body mass from European skeletal remains are all subject to various limitations. Here, we develop new prediction equations based on large skeletal samples representing much of the continent and temporal periods ranging from the Mesolithic to the 20th century. Anatomical reconstruction of stature is carried out for 501 individuals, and body mass is calculated from estimated stature and biiliac breadth in 1,145 individuals. These data are used to derive stature estimation formulae based on long bone lengths and body mass estimation formulae based on femoral head breadth. Prediction accuracy is superior to that of previously available methods. No systematic geographic or temporal variation in prediction errors is apparent, except in tibial estimation of stature, where northern and southern European formulae are necessary because of the presence of relatively longer tibiae in southern samples. Thus, these equations should bebroadly applicable to European Holocene skeletal samples.     

Methods for estimating missing human skeletal element osteometric dimensions employed in the revised fully technique for estimating stature

One of the greatest limitations to the application of the revised Fully anatomical stature estimation method is the inability to measure some of the skeletal elements required in its calculation. These element dimensions cannot be obtained due to taphonomic factors, incomplete excavation, or disease processes, and result in missing data. This study examines methods of imputing these missing dimensions using observable Fully measurements from the skeleton and the accuracy of incorporating these missing element estimations into anatomical stature reconstruction. These are further assessed against stature estimations obtained from mathematical regression formulae for the lower limb bones (femur and tibia). Two thousand seven hundred and seventeen North and South American indigenous skeletons were measured, and subsets of these with observable Fully dimensions were used to simulate missing elements and create estimation methods and equations. Comparisons were made directly between anatomically reconstructed statures and mathematically derived statures, as well as with anatomically derived statures with imputed missing dimensions. These analyses demonstrate that, while mathematical stature estimations are more accurate, anatomical statures incorporating missing dimensions are not appreciably less accurate and are more precise. The anatomical stature estimation method using imputed missing dimensions is supported. Missing element estimation, however, is limited to the vertebral column (only when lumbar vertebrae are present) and to talocalcaneal height (only when femora and tibiae are present). Crania, entire vertebral columns, and femoral or tibial lengths cannot be reliably estimated. Further discussion of the applicability of these methods is discussed.     

Growth and maturation of roker Raja clavata L. in the Solway Firth

Two hundred and seventy-one Raja clavata taken by otter trawl from the Solway Firth were examined for size, sex and state of maturity. Size relationships for both sexes were similar. Total length and disc width were linearly related as were disc width with wing width. Males and females appear to mature at 42 and 45 cm disc width respectively. The Solway population is heavily exploited by an unrestricted commercial fishery and a considerable proportion (48·6%) of the presently retained catch is immature. It is suggested that fishing pressure has brought about a reduction in the size at which female fish mature.     

Size and age at sexual maturity of Atlantic argentine,Argentina silus: a critique

Synopsis A recent analysis of size and age at sexual maturity ofArgentina silus on the Scotian Shelf is invalid because field maturity stage data collected during the non-spawning, quiescent stage of the reproductive cycle were unreliable for distinguishing between immature and resting mature stages. Thus two-thirds of the data used must be discounted. Utilization of different length measurement criteria for different years, for which no correction is made, could introduce substantial error in length at maturity estimates based on the remaining data. Age data collections were restricted to one 12 month period and thus were inadequate to characterize age at maturity by 5 yr time periods as attempted in this analysis. No attempt is made in the analysis to determine whether available samples adequately represent the population with regard to maturity i.e. whether immature and mature fish of the same length had an equal probability of being sampled. It is demonstrated here that maturity ogives can differ greatly depending on assumptions made concerning the representativeness of samples. Many of the criticisms made are likely valid for a series of papers on maturity of Atlantic coast fishes by the same author.     

Growth and skeletal maturation in British Columbia Indian Populations

Stature and skeletal maturation in childhood, mature stature, and calorie and protein intakes were studied in two populations of British Columbia Indians. Although mature stature was similar in both groups, one population (Anaham) showed delayed stature achieved for age and delayed skeletal maturity in childhood, compared with the other population (Ahousat). Analysis of growth data suggests that environmental factors are probably the predominant cause of the differences, which coincide with differences in nutritional status. Mean calorie intakes at Ahousat approximate or exceed the Canadian Dietary Standards, but those at Anaham are consistently below the standards for all age groups. Although mean protein intakes are well above the standards for all age groups, except teen-age girls at both reserves, they are consistently lower at Anaham than at Ahousat.     

Technical note: a re-evaluation of stature estimation from skeletal length in the grave

Several methods for stature estimation have been proposed over the years. Among these methods is anatomical reconstruction, regression based on long bone lengths, and measuring skeletal vertex - talus length in the grave for individuals buried in a supine position. Recent studies have dealt with the applicability of skeletal length in the grave (Petersen: Int J Osteoarchaeol 15 (2005) 106-114) and anatomical reconstruction (Raxter et al.: Am J Phys Anthropol 130 (2006) 374-384). The results from the latter study calls into question the results of the former study. Therefore an investigation of the potential bias of using skeletal length in the grave as an estimate of living stature has been performed. Twenty Medieval Danish skeletons were measured both in situ and in the laboratory, and the anatomically reconstructed stature (Raxter et al.: Am J Phys Anthropol 130 (2006) 374-384) was compared with the skeletal length in the grave. The results show that 2.5 cm should be added to skeletal length in the grave in order to obtain an unbiased estimate ofliving stature.