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.     

Some genetic traits in Solomon Island populations. 3. Relative toe length

Among 1,605 Solomon Islanders from four tribes, there was no sex difference in relative length of the first and second toes. In three of the tribes, longer first toes were slightly more frequent in persons over the age of 45. The percentages of longer first toes in the groups as a whole were 60.5% for Baegu, 66.4% for Nasioi, and 72.1% for Kwaio. These frequencies, resembling those reported for white Americans, Europeans, and single small samples of New Caledonians and Vietnamese, were much below those for Africans. The fourth tribe, the Lau, had only 37.1% with a longer first toe, the lowest percentage reproted so far around the world. No simple mode of single-gene inheritance was apparent, and polygenic inheritance is proposed.     

Hand clasping and arm folding in the Basque population

Hand clasping and arm folding have been analysed in 286 males and 455 females of the Basques. The results are compared with those from other Spanish populations. Examination of the association between hand clasping and arm folding shows a strong correlation between the right type of one and the left type of the other.     

Some genetic traits in Solomon Island populations. V. Assortative mating, with special reference to skin color

Married couples in four Solomon Islands tribes did not mate assortatively for body size or shape. All four groups had high correlations (0.6 to 0.9) between spouses' age and moderate correlations, 0.3 to 0.5, for age-associated traits like nose height, ear length, and grayness of hair. Three brownskinned groups from Malaita (Kwaio, Lau, and Baegu) showed significant assortative mating for skin color whereas the very dark-skinned Nasioi, from Bougainville, did not. The positive correlations between spouses for skin color, with r's for various bodily regions ranging from 0.2 to 0.6 in the three Malaitan tribes, persisted when age was partialled out. As expected with assortative mating, the Malaitans' skin color was highly variable.     

Some genetic traits in Solomon island populations. I. Introduction: people and habitats

To introduce a set of genetic studies among Solomon Islanders, four tribal groups on Bougainville and Malaita Islands are described. They were observed in 1966 and 1968 by social anthropologists and biomedical scientists from Harvard University. The groups varied in habitat and way of life from fishermen living on artificial islets in a saltwater lagoon (the Lau, on Malaita) to shifting agriculturists (the Nasioi, on Bougainville, and the Kwaio and Baegu, on Malaita). The Nasioi were darker than the Malaitans and spoke a non-Austronesian rather than a Melanesian language; they were also more Westernized. Coverage of residents in designated hamlets ranged from 78% to over 95%. In all, 1,626 persons were studied: 256 Nasioi, 443 Kwaio, 442 Lau, and 485 Baegu. Genetic differences have been found between the Nasioi and the Malaitans, and between the Lau and the other Malaitans.     

Study on pottical type, palmar and plantar digital formulae, hand clasping, arm folding, handedness, leg folding and stride type in the Daur population, China

The pottical type, palmar and plantar digital formulae, hand clasping, arm folding, handedness, leg folding and stride type have been investigated on a sample of 143 male and 160 female students of the Daur population of Molidawa Banner, Inner Mongolia. The results of this study are the following: 1. the frequency of the hyperextensive pottical type is 49.17%, the relative length of index over annularis 12.21%, right hand clasping 45.87%, right arm folding 49.50%, right handedness 94.39%, right leg folding 72.28% and right stride type 44.88%, 2. pottical type, hand clasping, handedness, leg folding and stride type do not show significant sex differences, 3. there are some relations between hand clasping and arm folding as well as between arm folding and stride type, 4. compared with other population groups, the Daur population shows a low frequency of right hand clasping, a moderate frequency of right arm folding and a low frequency of left handedness.     

A Hungarian twin study on hand clasping, arm folding and tongue curling

A twin study was performed in adult Hungarian monozygotic and dizygotic pairs for hand clasping, arm folding and tongue curling. Genetic background of these traits could not be confirmed, although there appears to be a positive correlation between hand clasping type and handedness.     

Smoking and pulmonary function in five Solomon Island populations.

The relationship between smoking and lung function was examined in a large sample of healthy Solomon Island Melanesians and Polynesians as part of a multidisciplinary study carried out in 1985 and 1986. Comparisons are made between samples of smokers and non-smokers to determine if smoking is associated with a reduction in pulmonary function among males and females between 25 and 75 years of age. The results of this study indicate that cigarette smoking causes significant reductions in the pulmonary function of these populations. In addition, a clear difference in pulmonary function between males and females, as well as a general reduction in female FEV1 values, suggests that cooking smoke inhalation may be operating as a possible risk factor to the pulmonary health of women. Further research is needed to quantify exposure to smoke of both males and females and relate this measure to declines in pulmonary function.     

海南黎、苗、汉族扣手、交叉臂和惯用手的研究

调查了海南居住较为集中的黎、苗、汉族(共3 207人)扣手、交叉臂、惯用手等人类左右不对称行为特征。结果显示：(1)扣手、交手臂、惯用手三型3个民族的出现率均为R>L型,惯用手的R型出现率远较其他两型高,呈高度显著性差异,(P<0.01)。(2)扣手、交叉臂出现率与性别无关。(3)惯用手R型出现率苗族女性明显高于男性,差异显著(P<0.05)。三民族总和出现率为89.06％,是国内外属最低的。(4)扣手与交叉臂、扣手与惯用手,交叉臂与惯用手之间均具有相当明显的相关性。 Abstract：It was investigated that three types of many general indexes of anthrotogical genetics,which include hand-clasping、arm-folding and handedness,just among Li,Miao and Han nationalities in Hainan.There were 3207 people investigated in total.The results showed as follows:(1)The frequency of hand?clasping,arm-folding and handedness is far higher than others(P<0.01).(2) It was proved that there was no signilicant difference between male and female in the frequency of either hand-clasping or arm-floding.(3)It was obvious that the frequency of type R handedness in female of Miao nationality was higher than in male.And the difference was much clear(P<0.05).The total frequency of handedness was about 89.06 percent,which was the lowest rate as far as we known.(4)There was correlation among handedness and hand?clasping,handedness and arm-folding andhand-clasping and arm-folding respectively.     

Mitochondrial and nuclear genetic relationships among Pacific Island and Asian populations.

Mitochondrial and autosomal short tandem-repeat (STR) genetic distances among 28 Pacific Island and Asian populations are significantly correlated (r=.25, P<.01) but describe distinct patterns of relationships. Maternally inherited-mtDNA data suggest that Remote Oceanic Islanders originated in island Southeast Asia. In contrast, biparental STR data reveal substantial genetic affinities between Remote Oceanic Islanders and Near Oceanic populations from highland Papua New Guinea and Australia. The low correlation between maternal and biparental genetic markers from the same individuals may reflect differences in genome-effective population sizes or in sex-biased gene flow. To explore these possibilities, we have examined genetic diversity, gene flow, and correlations among genetic, linguistic, and geographic distances within four sets of populations representing potential geographic and cultural spheres of interaction. GST estimates (a measure of genetic differentiation inversely proportional to gene flow) from mtDNA sequences vary between 0.13 and 0.39 and are typically five times greater than GST estimates from STR loci (0.05-0.08). Significant correlations (r>.5, P<.05) between maternal genetic and linguistic distances are coincident with high mtDNA GST estimates (>0.38). Thus, genetic and linguistic distances may coevolve, and their correspondence may be preserved under conditions of genetic isolation. A significant correlation (r=.65, P<.01) between biparental genetic and geographic distances is coincident with a low STR GST estimate (0.05), indicating that isolation by distance is observed under conditions of high nuclear-gene flow. These results are consistent with an initial settlement of Remote Oceania from island Southeast Asia and with extensive postcolonization male-biased gene flow with Near Oceania.     

The role of migration in the genetic structure of populations in temporally and spatially varying environments II. Island Models

The Island Model introduced by Sewall Wright (1951) has proven to be a useful construction for studying the interaction of genetic drift, population subdivision, and mutation. Interest in the model has recently increased because of its relevance to certain questions involving the rate of differentiation of sub-populations under the neutral allele hypothesis (e.g., Smith, 1970; Latter, 1973). It is perhaps the only realistic population structure in which the test for neutrality proposed by Lewontin and Krakauer (1973) is valid (Lewontin and Krakauer, 1975). If data from natural populations is to be compared to the predictions of the Island Model, it is desirable to have an alternative model with the same migration pattern but with natural selection operating. In this paper one such model will be introduced where the stochastic element comes from random fluctuations in the environment rather than from genetic drift. The model is a direct extension of the one in the previous paper in this series (Gillespie, 1975) which dealt with a population which is subdivided into two patches with restricted migration between them.