Anthropometric studies of the long bones of the "shell mound" Indians

The “shell mound” Indians exhibit both sexual and bilateral variations in comparative long bone lengths. Mean long bone lengths are shortest in the Indian group when compared to those reported for both Caucasians and Negroes. The radiohumeral and humero-femoral indices of the “shell mound” Indians are higher than those reported for either Caucasians or Negroes. There is a relatively high degree of anterior-posterior curvature of the femur in the Indian group when compared to the femora of Caucasian and Negroes. There is apparently no correlation between maximum femoral length and trochanter length in comparing right and left sides in either sex. The collo-diaphyseal angles are greater on the average on the left side in both sexes. The femora of male “shell mound” Indians exhibits greater average collo-diaphyseal angles than do the femora of male Caucasians.     

Anterior femoral curvature: Its probable basis and utility as a criterion of racial assessment

Stewart ('62) and Walensky ('65) indicated that while the metrical expression of anterior femoral curvature alone will not always differentiate between Whites, American Negroes, and North American Indians, it was very useful as a racial criterion in combination with observed traits such as torsion, pilastry, and cross-sectional shape. Seven additional North American Indian groups reported here, representing both pre-Columbian and post-contact times, upheld the observation that anterior femoral curvature is a useful feature of racial assessment for Negroes, Whites and North American Indians. However, two South American groups studied (Ecuador and Peru) were only slightly more curved than American Negroes, and were less curved than Whites and North American Indians. The metrical expression of anterior femoral curvature therefore is not a useful feature of racial assessment for separating these two South American Indian groups from Whites and American Negroes. Femora of American Negro and White individuals with low ponderal indices were found to be less bowed than the norms for their race; individuals with high ponderal indices were more bowed than the norm for their race. The assumed genetic basis for expression of anterior femoral curvature suggested by Stewart ('62) and Walensky ('65) seems to be a feature of human plastic response to body weight rather than to temporal, clinal, postural or equestrian influences.     

Genetic variability among peoples of Aruba and Curaçao

Data were obtained from 252 elementary school pupils in four regions of Aruba and in the suburbs of Willemstad, Curaçao. Data included ABO and MN blood groups, ratings of skin color and hand prints. Pupils in the Noord region of Aruba differ significantly from those at other schools in both islands with respect to frequencies of MN blood group genes; mean ridge counts on fingers; and pattern frequencies in hypothenar and thenar/first interdigital palmar areas. Noord pupils have significantly darker skin color than those in other Aruban areas. No significant differences were encountered in ABO frequencies, which are more similar to those of Negroes than to American Indians and Caucasians. MN blood group frequencies and finger prints of pupils in the Noord region are similar to those of American Indians, whereas those in other regions are similar to those of Negroes and western Europeans.     

MICA polymorphism in South American Indians

We have studied the MICA alleles of 196 unrelated subjects from three South American Indian tribes (Toba, Wichi and Terena). They are members of isolated tribes located in the Gran Chaco area in northeastern Argentina and in Mato Grosso do Sul in South Central Brazil. Of 55 previously known alleles, nine were observed in South American Indians, compared with 16 that were found in North American Caucasians, suggesting a more restricted allelic distribution of MICA in these tribes. In South American Indians, MICA*00201 was the most frequent allele, with a gene frequency of 33% in Toba, 47% in Wichi and 44% in Terena. MICA*00201, MICA*027 (external domain sequence like MICA*008/TM allele A5) and MICA*010 accounted for more than 90% of all the MICA genes in South American Indians. In North American Caucasians, MICA*00801 (*008/A5.1) accounted for 42% of the genes and was the most common allele. We observed a high degree of linkage disequilibrium between certain alleles of MICA and of HLA-B in the South American Indian populations. Phylogenetic trees constructed using gene frequencies of the transmembrane short tandem repeats in the populations reported here, and in other populations taken from published reports, suggest that South American Indians are more closely related to Asians than to Europeans.     

Distribution of adenylate kinase and phosphoglucomutase isoenzymes in the population of the city of New York.

Blood samples from unrelated persons living in New York, N.Y., were examined for phosphoglucomutase (PGM) and adenylate kinase (AK) phenotypes, the sample consisting of 164 Caucasians, 133 Negroes, 129 persons of Spanish origin or descent, and 156 Chinese for PGM and 136 Caucasians, 134 Negroes, 136 persons of Spanish origin or descent, and 156 Chinese for AK. The PGM1 gene frequency was found to be 0.7774 for Caucasians, 0.8083 for Negroes, 0.7461 for Hispanic persons, and 0.7917 for Chinese. One Hispanic person had a very rare type, PGM 8-1-FAST. The AK1 gene frequency was found to be 0.9669 for Caucasians, 0.9813 for Negroes, 0.9779 for Hispanic persons, and 1.000 for Chinese.     

Some genetic traits in Solomon Island populations. IV. Mid-phalangeal hair

Among 425 Lau and 467 Baegu of northern Malaita, there were no tribal differences in mid-phalangeal hair. The trait was present more often in males than in females, and after puberty than before it. Age differences were more marked for males than for females. Among 168 men 20 years of age and older in both tribes, the frequency of mid-phalangeal hair was 58.3%; among 189 women of similar age, 34.4%. These frequencies were at or just below those reported for Caucasian samples, just above that for Japanese, and considerably above those for Negroes and American Indians. Analysis of family data did not confirm the hypothesis that the absence of mid-phalangeal hair is recessive to its presence.     

Ulnar polydactyly

A retrospective review of 148 patients with ulnar polydactyly was conducted to analyze the types, patterns of involvement, associated anomalies, treatments, and outcomes of this malformation. The hands only were involved in 123 patients, both hands and feet in 20 patients, and five patients had mixed radial and ulnar polydactyly. Ulnar polydactyly was more prevalent among males. Among African Americans, the condition was often bilateral. When unilateral, ulnar polydactyly occurred more often on the left side. The racial distribution was 103 African Americans (70 percent), 37 Caucasians (25 percent), four Native Americans, three Latin Americans, and one Asian. Five types were encountered: type I cutaneous nubbin, type II pedunculated digit, type III articulating digit with fifth metacarpal, type IV fully developed digit with sixth metacarpal, and type V polysyndactyly. The distribution of types in order of frequency was type II, III, V, I, and IV. Types I and II ulnar polydactyly combined were more prevalent (82 percent) than types III, IV, and V (18 percent). Types I and II were more common among African Americans. Types III, IV, and V ulnar polydactyly occurred more frequently among Caucasians, but these were slightly less prevalent than types I and II in this racial group. Five patients were syndromic; four were Caucasians, and one Asian. Most cases of ulnar polydactyly of the hand were treated by ligation (71 percent) in the nursery, whereas polydactyly of the foot was more often referred to a specialist to be treated by surgical ablation (92 percent). Treatment complications occurred more frequently in the hands than in the feet. The complication rate after ligation of ulnar polydactyly of the hand was 23.5 percent. The two main complications were tender or unacceptable nubbins and infections.     

Sex and race differences in finger ridge-count correlations

Correlations between ridge-counts on the ten fingers were compared by race and sex in 11 samples representing Negroes and Caucasians: five from subsaharan Africa, one American Black, three European, one American White and one from India. The samples of European ancestry showed no consistent sex difference in mean correlation, although female American Whites significantly exceeded males. In three of the six Negro samples and in the Parsis of India males showed significantly higher average correlations than females. The pattern of sex and race differences suggests that the sex chromosomes, particularly the Y chromosome, play a role in dermal ridge development.     

Rare variants, private polymorphisms, and locus heterozygosity in Amerindian populations.

The results of 21,103 electrophoretic typings distributed across 28 polypeptides in members of 12 Amerindian tribes are reported, and the accumulated results of electrophoretic studies on these same polypeptides in 21 Amerindian tribes are then analyzed. Thus far 11 'private' polymorphisms have been identified in these tribes. When the tribal samples are combined and traits achieving polymorphic proportions in the total sample excluded from consideration, the average frequency of rare variants is 2.8 per 1,000 determinations. For a subset of 23 of these polypeptides also studied in Caucasians and Japanese, variant frequencies per 1,000 determinations are: Indians, 2.2; Caucasians (British), 1.6; and Japanese, 1.5. Average locus heterogeneity for these polypeptides (based on rare variants plus polymorphisms) is: Indians, .049; Caucasians, .078; and Japanese, .077. A higher proportion of loci are monomorphic within tribes than within civilized urban populations. It is argued that for inferences concerning the forces maintaining genetic variability within populations, studies on samples from tribespeople are much more appropriate than studies on samples from civilized urban populations.     

Carpal fusions in children of four South African populations

The incidence of carpal fusions was determined from radiographs of both hands of 2,250 Pretoria schoolchildren aged 72 to 191 months. The group included White, Negro, Coloured and Indian subjects. Of the many possible varieties of carpal fusion, only lunato-triquetral fusion and capitate-hamate fusion were encountered. No examples of lunato-triquetral fusion were encountered in children less than ten years of age. In Pretoria Negroes aged 10 to 15 years, the incidence of lunato-triquetral synostosis is 4.57%, while Pretoria Coloureds show an incidence of 1.51%. This type of fusion was not noted in the White or Indian populations. Two examples of capitate-hamate synostosis were encountered in Pretoria Negroes. The available evidence suggests that these two varieties of carpal fusion may be added to the list of discrete traits varying in frequency from population to population and probably reflecting different underlying gene frequencies. No significant sex difference in incidence of lunato-triquetral fusion was noted in the present study. Lunato-triquetral fusion is about twice as commonly bilateral as unilateral in occurrence.     

The mylohyoid bridge in four population samples from India, with observations on its suitability as a genetic marker

Four adult skeletal samples from the states of Uttar Pradesh, Andhra Pradesh, and Bihar in India have been studied for the incidence of mylohyoid bridge. The incidence, varying between 2.98% and 7.14%, has been compared with frequencies reported for other populations of the world. The range of variation for Indians, as a whole, falls within the lower levels of the spectrum of worldwide variation for this trait, ranging between 0.47% for French Europeans and 33.8% observed among Plains American Indians. While noting its possible significance for clinical purposes, the suitability of the mylohyoid bridge as a population genetic marker has been discussed. It is emphasized that its use as a genetic marker in isolation of other discrete traits has serious limitations. For meaningful population definition and relationships as many discrete variants as possible ought to be utilized.     

Variation in the number of presacral vertebrae in bantu-speaking South African Negroes

Variation in number of presacral vertebrae (PSV) was examined in 462 vertebral columns in four populations drawn from tribal groups of Southern African Negroes. The total incidence of numerical variants (23 PSV and 25 PSV) was 19% in males and 12.1% in females. Males have a higher frequency of 25 PSV and females a higher frequency of 23 PSV, a sex difference reported by previous workers. Significant differences in the incidence of 25 PSV in males were present between S.A. Negroes, American Negroes and other racial groups. The total number of variants (23 PSV and 25 PSV) is significantly higher in S.A. Negro males (and higher but not significantly in females) than in the other groups; owing mainly to the findings in the Nguni-speaking sub-samples of the S.A. Negro. These findings support a previous suggestion based on combined-sex data that the frequency of numerical variations of PSV are characteristic of a population. It is suggested here that such frequencies are even more characteristic when males and females are considered separately.     

Indian time for nature? A multi-level approach to American Indian outdoor time in everyday life

Social scientists have utilized daily time use studies as one method of understanding everyday lives. The bulk of this research, usually quantitative, identifies broad racial, ethnic and gender differences. Yet, certain groups and questions are typically excluded in daily time use research. One such group is American Indians. To address this lacuna, we look at the deeply discussed view that American Indians are closer to nature than other US ethnic groups. We use a nationally representative sample of individual daily time use (American Time Use Survey; n?=?136,960) to look at leisure time outdoors. Our results show that American Indians report greater time spent outdoors but that this is only statistically significant for those who identify as exclusively American Indian (not for American Indians that are multi- and bi-racial). This study confirms previous qualitative research that suggests American Indians have a distinct relationship with nature.     

The mylohyoid bridge of pre-Columbian Peruvians

The frequency of expression of the mylohyoid bridge was studied in the skeletal remains of 122 Pre-Columbian Peruvians. The incidence in this population was found to be 17.6% as compared to an incidence of 15.4% found in a similar size sample population of American Negroes and a 16.1% incidence in a population of American Whites from the Terry Collection. No significant differences as to the incidence of the mylohyoid bridge were found as to the side of occurrence or between deformed and undeformed crania. A mylohyoid bridge was found in a younger individual (6 years) than had previously been reported. Females showed a significantly higher incidence of this trait in all three populations studied. A similar incidence of the mylohyoid bridge in Pre-Columbian and Mongoloid peoples adds support to the theory of a Mongoloid origin of these people. The mylohyoid bridge is considered to be a significant genetic marker which along with other such markers could be of value in population studies.     

Phenotypic distributions of red cell glutamate-pyruvate transaminase (E.C.2.6.1.2) isoenzymes in British and New York populations.

1444 persons of British nationality living in London, and 294 Caucasians, 258 Negroes, 310 Hispanic persons, and 151 Chinese persons living in New York were tested for glutamate-pyruvate transaminase phenotype. The Gpt1 frequency in the British population was found to be 0.5277, the Gpt2 frequency was 0.4716, and two GPT 3-2 persons were found. The Gpt1 frequencies in the New York population were: 0.4834 in Chinese; 0.5226 in Hispanic persons; 0.8101 in Negroes; and 0.5306 in Caucasians. Two Caucasians possessed the GPT 3-2 phenotype.     

The number of vertebrae in the Southern African Negro,the American Negro and the Bushman (San)

The numbers of precoccygeal vertebrae (PCV) are compared in Southern African Negroes, Bushman (San) and American Negroes. The S.A. Negro and San males have an exceptionally high frequency of an increased total PCV number whilst the frequencies are significantly lower in a combined Caucasoid sample and the Mongoloid samples. The American Negro male, too, has a high frequency but not as high as in S.A. Negroes. The high frequency of increased PCV number in San, S.A. Negroes and American Negroes is in keeping with the view that the Khoisan peoples (here represented by the San), the Southern African Negroes and the African ancestors of American Blacks sprang from a common proto-negriform stock. Males have a significantly greater frequency of increased PCV to 30 or 31, whereas females are more likely to have a decreased number of 28 PCV. This sex difference is present in all the populations studied.     

A study of some immunological and clinical characteristics of gastritis, gastric ulcer, and duodenal ulcer in three racial groups of the Venezuelan population

Circulating gastric-mucosa antibodies were found more frequently among patients with different forms of chronic gastritis than among a miscellaneous control group and groups that presented prepyloric ulcer or duodenal ulcer. A higher incidence of circulating antibodies and of chronic gastritis lesions among Caucasians and “Mestizos” than among Negroes was also observed. The latter showed a higher tendency to duodenal ulcer and prepyloric ulcer. The high incidence of gastritis and gastric ulcer of the Chinese and the Mestizos support the ethnic relation between these two human groups. Our study favors the hypothesis that genetic and ethnic factors influence, on the one hand, chronic gastritis and gastric ulcer and, on the other hand, duodenal and prepyloric ulcers.     

Genetic and population studies of quantitative levels of adenosine triphosphate in human erythrocytes

The mean content of ATP in red cells of American Negroes is significantly less than the mean level in American Caucasians. This is compatible with the hypothesis that the quantitative level of ATP in red cells may be involved in selective processes related to falciparum malaria. There is no evidence of a sex effect on levels of ATP in either population. Family studies conducted in both populations indicate that the quantitative level of red cell ATP is at least partially inherited. Studies of a number of biochemical characteristics of red cells have been conducted in an effort to elucidate the mechanism of genetic and biochemical control of quantitative levels of erythrocytic ATP. These studies have been negative. Although other studies have demonstrated that thalassemia trait influences the level of red cell ATP, the presence of sickle cell trait or G-6-PD deficiency, the other two systems postulated to be involved in malaria protection, did not result in significant differences in mean red cell ATP content.The work reported in this paper was supported in part by the Research and Development Command, Office of the Surgeon General, Department of the Army, under contract DA-49-193-MD-2855 with the Department of Medicine, University of Michigan. With respect to this support, it is contribution number 167 from the Army Research Program on Malaria. The work was also supported in part by USPHS grant AM 09381 and USPHS Career Development Award 1-K3-AM 7959.     

Glucose dehydrogenase polymorphism among ethnic groups of Singapore--with report of two additional alleles (GDH4 and GDH5).

Placental glucose dehydrogenase (GDH; E.C.1.1.1.47) polymorphism was studied in 254 Chinese, 104 Malays, and 47 Indians from Singapore using isoelectric focusing. There is suggestive evidence of two additional anodal alleles (GDH4 and GDH5) in addition to the three alleles described in earlier studies. Altogether, 14 phenotypes have been observed in the present investigation, compared with six phenotypes described in earlier studies. It appears that placental GDH is controlled by five codominant autosomal alleles producing 15 possible phenotypes. The gene frequencies of GDH1, GDH2, and GDH3 in these ethnic groups are significantly different from those reported in Caucasians. There were slight differences in the gene frequencies between the three ethnic groups, with those of Indians being nearer to the frequency in Caucasians. In general, the distribution of GDH phenotypes was at Hardy-Weinberg equilibrium in all three ethnic groups studied.     

Shortened fifth medial phalanges

A radiographic study was made of the left fifth medial phalanges of 200 Philadelphia Negro and 96 Chinese children. Twelve cases of abnormal shortening of this bone (defined, for the present, as less than half the length of the fourth medial phalanx) were found in the Chinese sample, while none were found in the Negroes. This trait, brachymesophalangy 5, in general seems to be characterized by short but well proportioned diaphyses and cone-shaped epiphyses with very early union. Population surveys reported in the literature indicate that this trait is considerably more common in Mongoloid and American Indian populations than in Whites or Negroes. The mode of inheritance of this genetic trait is uncertain, but present evidence indicates that it may be a simple autosomal recessive.