屯堡人7项不对称行为特征

在贵州省安顺市对359例屯堡人(男145例,女214例)中学生的7项不对称行为特征(扣手、利手、叠臂、叠腿、利足、起步类型和优势眼)进行了调查。研究结果显示:1)屯堡人除叠臂左型率高于右型率外,其他6项不对称行为特征均为右型率高于左型率;2)屯堡人7项不对称行为特征的出现率均无性别差异;3)与其他族群比较,屯堡人利足右型率和叠臂右型率中等,叠腿右型率和扣手右型率高;4)屯堡人两两不对称行为中,扣手与利手、扣手与叠臂、扣手与叠腿、叠腿与起步相关,利手、利足、起步三种行为彼此相关。     

汉族湘语族群的7项不对称行为特征

在湖南省娄底地区调查了汉族湘语族群507例(男269例、女238例)高中学生的7项不对称行为特征(扣手、利手、叠臂、叠腿、利足、起步类型和优势眼)。研究结果显示:1)湘语族群叠臂与起步类型L型率高于R型率, 其余5项均R型率高于L型率。2)湘语族群利手、叠臂、利足出现率存在性别间差异, 其余4项出现率均不存在性别间差异。3)在已发表的资料中, 湘语族群扣手和起步类型右型率中等偏高, 利手右型率处于中等水平, 叠臂和叠腿右型率低,利足和优势眼右型率高。4)主成分分析结果显示, 汉族各族群不对称行为特征有一定的共性, 相对接近于中国北亚类型族群, 而与南亚类型族群差距较大。中国族群间不对称行为特征的差异, 主要反映在叠臂率差异、利足率差异。     

中国木雅人、尔苏人、八甲人与空格人6项不对称行为的特征

对四川、云南尔苏人、木雅人、空格人、八甲人4个族群进行了6项不对称行为特征(扣手、利手、叠臂、利足、叠腿、起步)的调查,结果显示:1)4个族群中,仅尔苏人、木雅人、八甲人叠臂以L型出现率偏高以外,其余不对称行为特征均为R型出现率较高;2)4个族群6项不对称行为特征均不存在性别间差异,但木雅人、尔苏人与八甲人在扣手这一不对称行为特征上存在族群间差异,木雅人与空格人在叠臂这一不对称行为特征上存在族群间差异;3)统计分析了6项不对称行为特征之间的相关性,仅八甲人多数不对称行为特征之间存在相关性。     

兴安盟3个民族7种不对称行为特征的研究

于1998年9月对内蒙古兴安盟的汉、蒙古、朝鲜族调查了1852例（男875例,女977例）中学生的7种不对称行为特征（利手、扣手、叠臂、叠腿、起步类型、利足、利眼）。结果显示：（1）3个民族中多数不对称行为特征的右型出现率过半。（2）扣手、叠壁、起步类型的出现率存在一定的民族间差异,而其它4种行征的出现率无此差异。（3）多数特征的出现率男女间差异不显著。（4）不对称行为特征间具有相关的数量较多,程序较高,所有存在相关的特征间均表现为同侧组合特征类型为其亲合特征。     

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.     

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.     

Genetic studies of Pangwalas, Transhumant and Settled Gaddis. 4. Colour blindness, mid-phalangeal hair, ear lobe attachment and behavioural traits

Frequency distributions of colour blindness, midphalangeal hair, ear lobe attachment, hand clasping, arm folding, leg folding and handedness are reported for different population groups from Himachal Pradesh, North India, namely Pangwalas, Transhumant Gaddis (Brahmans, Rajputs and Scheduled Castes) and Settled Gaddis (Brahmans, Rajputs and Schedules Castes). An attempt has been made to compare the results of the present study within and between these groups as well as with the results of other reports from different population groups of India and Asia.     

Genetic associations between lateral signs.

Only a few authors examined several lateral asymmetries in families simultaneously. Seven lateralities (handedness, footedness, eyedness, earedness, hand clasping, arm folding and leg crossing) were examined in a sample of 292 biologically related parent-offspring triads and 36 sibling pairs. Analysis of the family data showed a significant association between parents and children in most lateralities. The frequency of left-sidedness increased with the number of left-sided parents. Only in the case of footedness and hand clasping there are no significant correlations. Additionally we investigated the inter-relationship between the lateralities in the parental generation. There is a relative strong relation especially among the functional asymmetries. The study analysed also the genetic association (linkage) according to McManus & Mascie-Taylor (1979) between seven different lateralized characteristics. It is shown that the lateral asymmetries correlate genetically relatively imperfectly with each other comparing the inter-relationship between the lateralities in the parental generation. This implicates a multigenetical and also multifactorial determination of laterality in human being.     

4 anthroposcopic markers in the Northern Greece population: hand folding, arm folding, tongue rolling and tongue folding

Four anthroposcopic traits, namely hand clasping, arm folding, tongue rolling and tongue curling have been studied in a total of 7763 individuals from Thessaloniki and its surroundings, representing a sample of the population of Northern Greece. The statistical analysis of the data indicates significant sex differences only concerning tongue rolling. The frequencies obtained for the four traits under study are compared with data from the literature.     

Medicogenetic study of isolates in Uzbekistan. II. Anthropogenetic characteristics, blood groups and serum proteins]

A study is carried out on the distribution of ABO, MN, Rh, P and Le blood groups systems, haptoglobins, and common anthropogenetic features in the population of two villages of the Samarkand district. The examined samples have appeared to be heterogenous for ABO, Rh and P systems. For MN and Le unification is possible. The summary data on the allotment of phenotypes are as follows: (%) 0-30.2, A-35.3, B-26.2, AB-8.3, M-33.9, N-26.2, MN-39.9, Rh- -1.5, P-78.6, Le(a-b+)-33, Le (a+b-)-22.2, Le(a-b-)-34.2, Le(a+b+)-10.6. Gene frequencies have are calculated. The occurrence with regards to haptoglobins in both the villages is the same. The summary data are as follows: Hp1=1-4.8, Hp1=2-36.2, Hp2=2-59%. Gene frequencies have been calculated. In the population of the village Karakent there is a change of the frequency in many features of dermatoglyphics. The frequencies of anthropogenetic features do not differ between the villages. The summary data are the following: the frequency of theelbow type of hand is 86.9%, the right type of "hand clasping"-55.0%, the right type of "arm folding"-50.4%, righthandedness-99.7%. The occurence of square lobe of the ear is 21%, spliced one is 26.2%, the hanging down is 52.7%. The frequency of the gene insensitivity for PTC taste is 0.47 in one village and 0.53 in the other.     

Hand clasping--an overview]

The literature concerning the asymmetry clasping hands is reviewed based on 192 studies. This paper describes the incidence, sex differences, age differences and genetical problems including twinning. The incidence of left hand clasping ranges from 30% to 75% (mean 43%). The review confirms the so-called east-west-gradient and there is a predominance of the left type in Europe. Age and sex differences are only small. There is only a small relationship between hand clasping and handedness. 18 authors examined hand clasping in families and 4 in twins. The family data suggest that hand clasping may be under genetic control, yet it is clear that no simple genetic model for the inheritance can be applied. Both monozygotic and dizygotic twins show a low concordance and the R-R, R-L and L-L pairs in monozygotic and dizygotic twins are in binomial distribution.     

Biology of the people of Sikkim, India. 2. Colour blindness, ear lobe attachment, mid-phalangeal hair and behavioural traits

14 population groups of Sikkim (India)--Lepchas (2), Bhutias (2), Sherpas, Tamangs, Gurungs, Mangars, Rais, Limboos/Subbas, Pradhans (Newars), Brahmans, Chhetris, Scheduled Castes--have been studied in regard of the intra- and intergroup variability of colour blindness, ear lobe attachment, mid-phalangeal hair and behavioural traits (tongue folding, hand clapsing, arm folding, leg folding, handedness). Some of these variables show a considerable distribution heterogeneity, which is discussed considering history and marriage patterns of these populations. As most of them are highly endogamous one can assume that this heterogeneity is caused by locally acting factors such as drift and/or founder effects, which could be preserved due to as good as lacking gene flow among the populations under study. Beyond that the Sikkim data are compared briefly with those reported for other Indian and Asiatic populations.     

贵州苗族5项遗传性状分析

调查贵州苗族111例(男54例,女57例)耳垂、发旋、双手嵌合、酒窝和惯用手5项遗传性状的基因频率。在贵州苗族群体中耳垂的隐性基因频率高于显性基因频率;发旋在两性中分布存在极显著差异(P0.05);贵州苗族5项遗传性状的基因频率与国内其他地区汉族和少数民族存在差异,贵州苗族具有独特遗传性状特征。     

Population genetics of the inhabitants of Northern European USSR. II. Blood group distribution and antropogenetic characteristics in 6 villages in Archangel Oblast]

The paper deals with the distribution of genetic markers (systems ABO, MN, Rh (D), Hp, PTC) and a number of demographic (folding of arms, hand clasping, tongue rolling, right- and left-handedness, of the type of ear lobe, of the types of dermatoglyphic patterns) in the inhabitants of 6 villages in the Mezen District of the Archangelsk Region of the RSFSR (river Peosa basin). The data presented in this work were obtained in the course of examination of over 800 persons. Differences in the interpretation of the results of generally adopted methods of statistical analysis of samples from small populations are discussed. Among the systems analysed in one third of all the cases there was a statistically significant deviation from Hardy-Weinberg's ratios. For the MN blood groups and haptoglobins this was caused by the excess of heterozygotes. The test of Hardy--Weinberg's ratios at the level of two-loci phenotypes revealed no statistically significant deviations either in separate villages or in all the villages taken together. The analysis of heterogeneity with respect to markers inherited according to Mendel's law revealed statistically significant differences between villages in all the systems except haptoglobins. A considerable heterogeneity in the distribution of family names, the frequencies of some of them varying from village to village from 0 to 90%. Statistically significant differences between villages were shown for all the anthropogenetic characters except arm folding, hand clasping and right-left-handedness. Considering the uniformity of the environmental pressure in the region examined, the heterogeneity of the population studied is apparently associated with a random genetic differentiation (genetic drift) and, possibly, with the effect of the progenitor.     

Brief communication: Captive gorillas are right‐handed for bimanual feeding

Predominance of right‐handedness has historically been considered as a hallmark of human evolution. Whether nonhuman primates exhibit population‐level manual bias remains a controversial topic. Here, we investigated the hypothesis that bimanual coordinated activities may be a key‐behavior in our ancestors for the emergence and evolution of human population‐level right‐handedness. To this end, we collected data on hand preferences in 35 captive gorillas (Gorilla gorilla) during simple unimanual reaching and for bimanual coordinated feeding. Unimanual reaching consisted of grasping food on the ground, while bimanual feeding consisted of using one hand for holding a food and processing the food item by the opposite hand. No population‐level manual bias was found for unimanual actions but, in contrast, gorillas exhibited a significant population‐level right‐handedness for the bimanual actions. Moreover, the degree of right‐handedness for bimanual feeding exceeds any other known reports of hand use in primates, suggesting that lateralization for bimanual feeding is robust in captive gorillas. The collective evidence is discussed in the context of potential continuity of handedness between human and nonhuman primates. Am J Phys Anthropol 2010. © 2009 Wiley‐Liss, Inc.     

鄂伦春、鄂温克、达斡尔族一侧优势功能特征研究

报道了鄂伦春、鄂温克、达斡尔族7项一侧优势功能特征(扣手、利手、叠臂、叠腿、起步类型、优势足、优势眼)。结果显示,3个民族7项特征的左右型分布规律有较多的相似之处,绝大多数特征与性别无关。鄂温克族和达斡尔族的利手与叠腿、优势足、起步类型间均具明显关联,其腿足特征间的相关程度亦优于手臂特征。鄂伦春族则不然。 Abstract:Authors reported 7 traits of lateral functional dominance including hand clasping,handedness,arm folding,leg folding,stride type,foot preference and eye preference in Oroqen,Ewenki and Daur nationalities.The results showed as follws;(1)Among three nationalities their left and right distributive patterns of the traits had many similarities and there was no relation between most traits and sexes.(2)There were obvious corelations between handedness and leg folding,handedness and foot preference,handedness and stride type in Eweike and Daur nationalities.Compared with the traits of leg-foot with interrelation,the traits of hand-arm had little degree on correlation in Ewenki and Daur.(3)There was correlation between eye preference and hand clasping but no relation between handedness and hand clasping.     

The building block folding model and the kinetics of protein folding.

Here we show that qualitatively, the building blocks folding model accounts for three-state versus the two-state protein folding. Additionally, it is consistent with the faster versus slower folding rates of the two-state proteins. Specifically, we illustrate that the building blocks size, their mode of associations in the native structure, the number of ways they can combinatorially assemble, their population times and the way they are split in the iterative, step-by-step structural dissection which yields the anatomy trees, explain a broad range of folding rates. We further show that proteins with similar general topologies may have different folding pathways, and hence different folding rates. On the other hand, the effect of mutations resembles that of changes in conditions, shifting the population times and hence the energy landscapes. Hence, together with the secondary structure type and the extent of local versus non-local interactions, a coherent, consistent rationale for folding kinetics can be outlined, in agreement with experimental results. Given the native structure of a protein, these guidelines enable a qualitative prediction of the folding kinetics. We further describe these in the context of the protein folding energy landscape. Quantitatively, in principle, the diffusion-collision model for the building block association can be used. However, the folding rates of the building blocks and traps in their formation and association, need to be considered.     

Structural features of protein folding nuclei

A crucial event of protein folding is the formation of a folding nucleus. We demonstrate the presence of a considerable coincidence between the location of folding nuclei and the location of so-called "root structural motifs", which have unique overall folds and handedness. In the case of proteins with a single root structural motif, the involvement in the formation of a folding nucleus is in average significantly higher for amino acids residues that are in root structural motifs, compared to residues in other parts of the protein. The tests carried out revealed that the observed difference is statistically reliable. Thus, a structural feature that corresponds to the protein folding nucleus is now found.     

Right‐ and left‐handed three‐helix proteins. I. Experimental and simulation analysis of differences in folding and structure

Despite the large number of publications on three‐helix protein folding, there is no study devoted to the influence of handedness on the rate of three‐helix protein folding. From the experimental studies, we make a conclusion that the left‐handed three‐helix proteins fold faster than the right‐handed ones. What may explain this difference? An important question arising in this paper is whether the modeling of protein folding can catch the difference between the protein folding rates of proteins with similar structures but with different folding mechanisms. To answer this question, the folding of eight three‐helix proteins (four right‐handed and four left‐handed), which are similar in size, was modeled using the Monte Carlo and dynamic programming methods. The studies allowed us to determine the orders of folding of the secondary‐structure elements in these domains and amino acid residues which are important for the folding. The obtained data are in good correlation with each other and with the experimental data. Structural analysis of these proteins demonstrated that the left‐handed domains have a lesser number of contacts per residue and a smaller radius of cross section than the right‐handed domains. This may be one of the explanations of the observed fact. The same tendency is observed for the large dataset consisting of 332 three‐helix proteins (238 right‐ and 94 left‐handed). From our analysis, we found that the left‐handed three‐helix proteins have some less‐dense packing that should result in faster folding for some proteins as compared to the case of right‐handed proteins.Proteins 2013; © 2013 Wiley Periodicals, Inc.     

Resonant frequencies of arms and legs identify different walking patterns

The present study is aimed at investigating changes in the coordination of arm and leg movements in young healthy subjects. It was hypothesized that with changes in walking velocity there is a change in frequency and phase coupling between the arms and the legs. In addition, it was hypothesized that the preferred frequencies of the different coordination patterns can be predicted on the basis of the resonant frequencies of arms and legs with a simple pendulum model. The kinematics of arms and legs during treadmill walking in seven healthy subjects were recorded with accelerometers in the sagittal plane at a wide range of different velocities (i.e., 0.3-1. 3m/s). Power spectral analyses revealed a statistically significant change in the frequency relation between arms and legs, i.e., within the velocity range 0.3-0.7m/s arm movement frequencies were dominantly synchronized with the step frequency, whereas from 0.8m/s onwards arm frequencies were locked onto stride frequency. Significant effects of walking speed on mean relative phase between leg and arm movements were found. All limb pairs showed a significantly more stable coordination pattern from 0.8 to 1.0m/s onwards. Results from the pendulum modelling demonstrated that for most subjects at low-velocity preferred movement frequencies of the arms are predicted by the resonant frequencies of individual arms (about 0.98Hz), whereas at higher velocities these are predicted on the basis of the resonant frequencies of the individual legs (about 0.85Hz). The results support the above-mentioned hypotheses, and suggest that different patterns of coordination, as shown by changes in frequency coupling and phase relations, can exist within the human walking mode.