Genetic and socio-cultural differentiation in the aborigines of Arnhem Land, Australia

Four tribes of Arnhem Land were surveyed for dermatoglyphics; based on pattern intensity indices, total ridge-counts, and a distance statistic combining the two, it was shown that the tribes can be arranged into western (Tiwi, Gunwinggu) and eastern (“Murngin” and Andilyaugwa) groups. This substantiates observations made on Arnhem Land by linguists and social anthropologists. From a survey of allele frequency traits of blood factors and P.T.C. tasting, distance statistics were computed between the four tribes. These confirmed the relative isolation of the extreme Arnhem Land tribes. Distance statistics were also computed between the four tribes and two Central Australian tribes, the Aranda and Wailbri. The Aranda and “Murngin” were relatively close together agreeing with theories that the Aranda are derived from a not too remote southwards migration from north Arnhem Land, as supported by linguistic data. Correlations between the biological, geographical and linguistic distances were positive, and generally agreed with the expectation that socio-cultural and linguistic barriers are important in regulating gene flow between populations. This study emphasizes the need to consider biological distances in association with ecological and socio-cultural factors.     

Palm and sole interdigital ridge-count correlations

Correlations among the twelve palm and sole interdigital ridge-counts were calculated for samples of Europeans of German, Austrian, Finnish and Polish ancestry, for Bantu speaking Black Africans from Angola and the Republic of South Africa, for Japanese and Tibetans and for Indians and Coloureds from the Republic of South Africa. Canonical correlation and factor analyses were used to discern patterning in the correlations. Generally, within palm and within sole correlations are stronger than palm-sole correlations. However, the results show an unequivocal positive relationship between palm and sole ridge-counts. A consistent feature was a stronger relationship of palm c-d counts to sole a-b counts. We suggest that this pattern of correlation may reflect early morphogenetic pattern formation prior to commitment of cells to hands and feet.     

Structured exploratory data analysis (SEDA) of finger ridge-count inheritance: II. Association arrays in parent-offspring and sib-sib pairs

Familial similarity of the dermatoglyphic trait values of finger ridge-count scores and pattern intensity index is examined for 125 nuclear families from the Velanadu Brahmin population of Southern India by the method of association arrays. This methodology assesses parent-offspring and sibship similarity through a collection of measures of dependence that is sensitive to a variety of nonlinear trends and stochastic relationships between trait values. The method is used in conjunction with various weights to determine the relationship between family size and the level and form of dependence. These analyses reveal that siblings are most strongly associated for ridge-counts of the middle digit and less associated for the thumb and fifth digit ridge-counts. Further, sibship similarity for ridge-counts increases with family size for the thumb and fifth digit but remains relatively constant over all family sizes for the middle finger. Family size effects are also observed for total ridge-counts of the left hand, right hand, and both hands combined, and for the pattern intensity index. These effects of family size may be due to the most pronounced changes occurring in the amniotic environment between the first and second pregnancy, which are most strongly manifested in the sibship associations of smaller families.     

Permutation methods for the structured exploratory data analysis (SEDA) of familial trait values.

A collection of functions that contrast familial trait values between and across generations is proposed for studying transmission effects and other collateral influences in nuclear families. Two classes of structured exploratory data analysis (SEDA) statistics are derived from ratios of these functions. SEDA-functionals are the empirical cumulative distributions of the ratio of the two contrasts computed within each family. SEDA-indices are formed by first averaging the numerator and denominator contrasts separately over the population and then forming their ratio. The significance of SEDA results are determined by a spectrum of permutation techniques that selectively shuffle the trait values across families. The process systematically alters certain family structure relationships while keeping other familial relationships intact. The methodology is applied to five data examples of plasma total cholesterol concentrations, reported height values, dermatoglyphic pattern intensity index scores, measurements of dopamine-beta-hydroxylase activity, and psychometric cognitive test results.     

Dermatoglyphic variation among Finno-Ugric speaking populations: methodological alternatives.

Utilization of dermatoglyphics for population studies is apparently increasing, but methods vary widely among investigators. We investigate how different types of dermatoglyphic data can affect estimates of biological distance among Finno-Ugric speaking populations. Dermatoglyphic distances were calculated using the following categories of traits: 1) Finger ridge-counts (radial and ulnar count for each digit), 2) finger ridge-counts (largest count for each digit), 3) finger pattern types, 4) palm ridge-counts, 5) palm patterns, and 6) main-line terminations. In addition, we compare our distances with those of Heet, which rely heavily on summary characters. Distances are evaluated by comparing them to each other and to language and geographic distances. There is considerable variation in the pattern of relationships resulting from the different variable sets. Finger variables, whether ridge-counts or pattern classifications, agree well with each other. Palm patterns, main-lines, and finger variables show moderate agreement with each other, while palm ridge-counts agree poorly with all variable sets except main-lines. Heet's distances agree poorly with all other dermatoglyphic distances. Finger patterns and main-lines are most closely related to language distances, after controlling for geography, while correlations with geography generally disappear after controlling for language. Heet's distances have weak associations with language and geography. Finger variables and palm main-lines yield results which agree best with historical relationships among Finno-Ugric populations. Our results make it very clear that utilization of dermatoglyphics in population studies requires careful consideration of methods, and that summary measures of quantitative or qualitative data should be used with caution.     

Finger dermatoglyphics of the Tibetans

Finger prints of 156 Tibetan males and 150 females have been analyzed. Whorls are more abundant in Tibetan males (60.24%) than in females (48.67%). The index of pattern intensity shows a higher value in males (15.95) than the females (14.65). The bimanual differences (both in males and females) are not statistically significant for the occurrence of pattern on the digits of the right and left hands. However, the difference between the sexes for the occurrence of patterns on the finger balls, are statistically significant. Ridge counting was done for each finger. On all fingers, Tibetan males have higher ridge-counts than females. The possible tendency for the right hands to possess higher ridge-counts cannot be demonstrated statistically. Tibetans show greater affinity with the Southern Mongoloids in the frequency distributions of pattern types on the finger balls. However, a more detailed dermatoglyphic study of all the Mongoloid populations in South East Asia, Central Asia and Far East would yield information of great value in disclosing the palmar pattern distributions among the Mongoloids.     

An evaluation of three statistics of structured exploratory data analysis

The power of structured exploratory data analysis (SEDA) to discriminate among major genic, polygenic, and nongenetic determination of phenotypes was investigated using computer simulation. Three classes of SEDA indices (the major gene index, the offspring between parents function, and the midparent-child correlation coefficient) were evaluated. These three statistics, in combination, were reasonably sensitive in detecting the presence of a major locus and in discriminating between phenotypes with genetic effects and those with no genetic component. However, they were unable to discriminate between major genic and polygenically determined phenotypic models.     

Is horizontal transmission really a problem for phylogenetic comparative methods? A simulation study using continuous cultural traits

Phylogenetic comparative methods (PCMs) provide a potentially powerful toolkit for testing hypotheses about cultural evolution. Here, we build on previous simulation work to assess the effect horizontal transmission between cultures has on the ability of both phylogenetic and non-phylogenetic methods to make inferences about trait evolution. We found that the mode of horizontal transmission of traits has important consequences for both methods. Where traits were horizontally transmitted separately, PCMs accurately reported when trait evolution was not correlated even at the highest levels of horizontal transmission. By contrast, linear regression analyses often incorrectly concluded that traits were correlated. Where simulated trait evolution was not correlated and traits were horizontally transmitted as a pair, both methods inferred increased levels of positive correlation with increasing horizontal transmission. Where simulated trait evolution was correlated, increasing rates of separate horizontal transmission led to decreasing levels of inferred correlation for both methods, but increasing rates of paired horizontal transmission did not. Furthermore, the PCM was also able to make accurate inferences about the ancestral state of traits. These results suggest that under certain conditions, PCMs can be robust to the effects of horizontal transmission. We discuss ways that future work can investigate the mode and tempo of horizontal transmission of cultural traits.     

Complex segregation analysis of body height,weight and BMI in pedigree data from Middle Dalmatia,Croatia

It has recently been reported that the mode of inheritance of body height, weight and BMI in five ethnically and geographically different populations can be described in terms of a major gene (MG) model. Here, using the pedigree sample from the island populations of Middle Dalmatia, Croatia (1,312 observed individuals in 462 pedigrees), the evidence is presented that supports the above findings. By applying the usual transmission probability tests, the hypothesis has been accepted that a significant part of the variation of each one of those three basic morphological traits can be attributed to the effect of a putative large-effect gene. The effect of a putative MG is responsible for 39-50% of age and sex adjusted trait's variation and for 34-48% of the total (non age-adjusted) variation of height, weight and BMI.     

Familial true hermaphroditism: paternal and maternal transmission of true hermaphroditism (46,XX) and XX maleness in the absence of Y-chromosomal sequences

We report on 46,XX true hermaphroditism and 46,XX maleness coexisting in the same pedigree, with maternal as well as paternal transmission of the disorder. Molecular genetic analysis showed that both hermaphrodites as well as the 46,XX male were negative for Y-chromosomal sequences. Thus, this pedigree is highly informative and allows the following conclusions: first, the maternal as well as paternal transmission of the disorder allows the possibility of an autosomal dominant as well as an X-chromosomal dominant mode of inheritance; second, testicular determination in the absence of Y-specific sequences in familial 46,XX true hermaphrodites as well as in 46,XX males seems to be due to the varying expression of the same genetic defect; and third, there is incomplete penetrance of the defect.     

Genetic parameters of dermal patterns of ridge counts.

Dermatoglyphic traits including ridge counts and pattern type counts on fingers were studied in 711 families representing six racial groups in Hawaii. Heritability tesimates were derived from regressions of offspring on father, mother and mid-parent values as well as from full-sib correlations. These estimates varied from 0.23 for radial loops to 0.80 for total ridge count. The heritability estimates were lower for ridge counts of single hands or single digits.     

Genetics of host plant use and life history in the comma butterfly across Europe: varying modes of inheritance as a potential reproductive barrier

Comma butterflies (Nymphalidae: Polygonia c-album L.) from one Belgian site and three Spanish sites were crossed with butterflies from a Swedish population in order to investigate inheritance of female host plant choice, egg mass and larval growth rate. We found three different modes of inheritance for the three investigated traits. In line with earlier results from crosses between Swedish and English populations, the results regarding female oviposition preference (choice between Urtica dioica and Salix caprea) showed X-linked inheritance to be of importance for the variation between Sweden and the other sites. Egg mass and growth rate did not show any sex-linked inheritance. Egg mass differences between populations seem to be controlled mainly by additive autosomal genes, as hybrids showed intermediate values. The growth rates of both hybrid types following reciprocal crossings were similar to each other but consistently higher than for the two source populations, suggesting a nonadditive mode of inheritance which is not sex-linked. The different modes of inheritance for host plant preference vs. important life history traits are likely to result in hybrids with unfit combinations of traits. This type of potential reproductive barrier based on multiple ecologically important traits deserves more attention, as it should be a common situation for instance in the early stages of population divergence in host plant usage, facilitating ecological speciation.     

Common major gene inheritance of extreme overweight

We studied 3925 individuals in 961 families to determine the mode of inheritance of overweight. As an index of overweight, we examined body mass index. Our analyses indicate that the most likely genetic model for susceptibility to overweight included moderate polygenic inheritance (34% of variance resulting from many genes with small effects) and common (21% frequency) recessively expressed major genes (a few genes with large effects on the individuals who possess them). Standard statistical criteria for accepting both polygenic and major gene inheritance were met, including tests of Mendelian transmission. These results suggest that recessive major gene inheritance of overweight may be common and that homozygosity for overweight susceptibility alleles often results in overweight. Clinical, biologic, and empirical observations all suggest genetic heterogeneity, that is, more than one predisposing gene.     

A G matrix analogue to capture the cumulative effects of nongenetic inheritance

The genetic variance‐covariance ( G ) matrix describes the variances and covariances of genetic traits under strict genetic inheritance. Genetically expressed traits often influence trait expression in another via nongenetic forms of transmission and inheritance, however. The importance of non‐genetic influences on phenotypic evolution is increasingly clear, but how genetic and nongenetic inheritance interact to determine the response to selection is not well understood. Here, we use the ‘reachability matrix’ – a key analytical tool of geometric control theory – to integrate both forms of inheritance, capturing how the consequences of generation‐lagged maternal effects accumulate. Building on the classic Lande and Kirkpatrick model that showed how nongenetic (maternal) inheritance fundamentally alters the expected path of phenotypic evolution, we make novel inferences through decomposition of the reachability matrix. In particular, we quantify how nongenetic inheritance affects the distribution (orientation and shape) of ellipses of phenotypic change and how these distributions influence subsequent evolution. This interweaving of phenotypic means and variances accumulates generation by generation and is described analytically by the reachability matrix, which acts as an analogue of G when genetic and nongenetic inheritance both act.     

Circumfacial Markings in Siamang and Evolution of the Face Ring in the Hylobatidae

The occurrence of a white brow band in siamang is documented for the first time. The characteristic occurs in 4.4% of 250 siamang. Among adult siamang the characteristic occurs more often in females than in males (11.3% of 71 females vs. 1.4% of 73 males). In a particular family lineage of captive siamang (not included in the numbers above), the characteristic was unusually frequent (42.9% of 14). The trait appears to be inherited, possibly as an autosomal dominant inheritance. Additional white markings occur in at least one of the subjects on hands, feet, and in a corona above the ears. In contrast to other studies, our results suggest that the presence of white facial markings, and possibly also of white hands and feet and of a bright corona are primitive gibbon traits. In addition, some degree of sexual dichromatism in the circumfacial markings appears to have occurred in the common ancestor of all gibbons.     

Patterns of mitochondrial inheritance in the myxogastrid Didymium iridis

Seven strains of the Central American A1 mating series of Didymium iridis were crossed in all possible combinations. Individual plasmodia were isolated and grown to a stage where total DNA could be isolated for DNA-DNA hybridization with cloned mitochondrial DNA probes to determine the pattern of mitochondrial inheritance. Random, biased, and dominant patterns of uniparental mitochondrial inheritance were observed, as well as rare cases of biparental inheritance, depending on the particular parental strains mated. The diverse patterns suggest that the factors controlling mitochondrial inheritance in D. iridis are complex. Differences between trials of the same matings suggest that non-genetic factors may also influence mitochondrial inheritance.     

Alcohol dehydrogenase activities and ethanol tolerance in Anastrepha (Diptera, Tephritidae) fruit-fly species and their hybrids

The ADH (alcohol dehydrogenase) system is one of the earliest known models of molecular evolution, and is still the most studied in Drosophila. Herein, we studied this model in the genus Anastrepha (Diptera, Tephritidae). Due to the remarkable advantages it presents, it is possible to cross species with different Adh genotypes and with different phenotype traits related to ethanol tolerance. The two species studied here each have a different number of Adh gene copies, whereby crosses generate polymorphisms in gene number and in composition of the genetic background. We measured certain traits related to ethanol metabolism and tolerance. ADH specific enzyme activity presented gene by environment interactions, and the larval protein content showed an additive pattern of inheritance, whilst ADH enzyme activity per larva presented a complex behavior that may be explained by epistatic effects. Regression models suggest that there are heritable factors acting on ethanol tolerance, which may be related to enzymatic activity of the ADHs and to larval mass, although a pronounced environmental effect on ethanol tolerance was also observed. By using these data, we speculated on the mechanisms of ethanol tolerance and its inheritance as well as of associated traits.     

Heterogeneous pollen in Chlorophytum comosum, a species with a unique mode of plastid inheritance intermediate between the maternal and biparental modes

The majority of angiosperms display maternal plastid inheritance. The cytological mechanisms of this mode of inheritance have been well studied, but little is known about its genetic relationship to biparental inheritance. The angiosperm Chlorophytum comosum is unusual in that different pollen grains show traits of different modes of plastid inheritance. About 50% of these pollen grains exhibit the potential for biparental plastid inheritance, whereas the rest exhibit maternal plastid inheritance. There is no morphological difference between these two types of pollen. Pollen grains from different individuals of C. comosum all exhibited this variability. Closer examination revealed that plastid polarization occurs, with plastids being excluded from the generative cell during the first pollen mitosis. However, the exclusion is incomplete in 50% of the pollen grains, and the few plastids distributed to the generative cells divide actively after mitosis. Immunoelectron microscopy using an anti-DNA antibody demonstrated that the plastids contain a large amount of DNA. As there is a considerable discrepancy between the exclusion and duplication of plastids, resulting in plastids with opposite fates occurring simultaneously in C. comosum, we propose that the species is a transitional type with a mode of plastid inheritance that is genetically intermediate between the maternal and biparental modes.     

THE EVOLUTION OF MATERNAL CHARACTERS

We develop quantitative-genetic models for the evolution of multiple traits under maternal inheritance, in which traits are transmitted through non-Mendelian as well as Mendelian mechanisms, and maternal selection, in which the fitness of offspring depends on their mother's phenotype as well as their own. Maternal inheritance results in time lags in the evolutionary response to selection. These cause a population to evolve for an indefinite number of generations after selection ceases and make the rate and direction of evolution change even when the strength of selection and parameters of inheritance remain constant. The rate and direction of evolution depend on the inheritance of traits that are not under selection, unlike under classical Mendelian inheritance. The models confirm earlier findings that the response to selection can be larger or smaller than what is possible with simple Mendelian inheritance, and even in a direction opposite to what selection favors. Maternal selection, in which a mother's phenotype influences her offspring's fitness, is frequency-dependent and can cause a population to evolve maladaptively away from a fitness peak, regardless of whether traits are transmitted by Mendelian or maternal inheritance. Maternal selection differs from other forms of selection in that its force depends not only on the fitness function but also on the phenotypic resemblance of parents and offspring.