Distribution of epidermal ridge minutiae

The distribution of epidermal ridge minutiae on the distal portion of male human thumbprints has been characterized. For each of 412 thumbprints, a centrally located focal minutia was chosen and neighboring minutiae were sampled. Minutiae were considered to be neighbors if there were no other minutiae appearing in the intervening region defined by the two minutia events and the ridge system. For each neighbor minutia, the total ridge distance between the focal and neighbor minutiae was measured. This distance is the total length of ridges appearing in the intervening region. The number of neighbor minutiae occurring about the focal minutia was found to be normally distributed with a mean of 6.42 (n = 412). The distribution of total ridge distances was not adequately described by the negative exponential distribution, but was well described by a gamma distribution with a shape parameter of 0.193 and a scale parameter of 5.91 mm. This gamma distribution reflects a local overdispersion of minutiae. This study is noteworthy as the first to describe the distribution of epidermal ridge minutiae within the ridge structure. The results support prior work based on quadrat sampling and eliminate two possible sources of error. A possible explanation for the overdispersed distribution lies in the growth stress model for minutia formation. Minutia formation may alleviate local growth stress, thereby removing the impetus for formation of additional minutiae in the immediately surrounding region.     

Familial Resemblance in Eating Behaviors in Men and Women from the Quebec Family Study

Objective: It is commonly recognized that genetic, environmental, behavioral, and social factors are involved in the development of obesity. The family environment may play a key role in shaping children's eating behaviors. The purpose of this study was to estimate the degree of familial resemblance in eating behavioral traits (cognitive dietary restraint, disinhibition, and susceptibility to hunger). Research Methods and Procedures: Eating behavioral traits were assessed with the Three‐Factor Eating Questionnaire in 282 men and 402 women (202 families) from the Quebec Family Study. Familial resemblance for each trait (adjusted for age, sex, and BMI) was investigated using a familial correlation model. Results: The pattern of familial correlation showed significant spouse correlation for the three eating behavior phenotypes, as well as significant parent‐offspring and sibling correlations for disinhibition and susceptibility to hunger. According to the most parsimonious model, generalized heritability estimates (including genetic and shared familial environmental effects) reached 6%, 18%, and 28% for cognitive dietary restraint, disinhibition, and susceptibility to hunger, respectively. Discussion: These results suggest that there is a significant familial component to eating behavioral traits but that the additive genetic component appears to be small, with generalized heritability estimates ranging from 6% to 28%. Thus, non‐familial environmental factors and gene‐gene and gene‐environmental interactions seem to be the major determinants of the eating/behavioral traits.     

Resolution of genetic and uterine environmental effects in a family study of new dermatoglyphic measure: sole pattern ridge counts

The heritability of sole pattern ridge counts was examined in two family studies of endogamous castes from peninsular India. The phenotypes included ridge counts for each of the eight configurational areas separately, all areas combined, and only distal areas combined. Differences in heritability estimates were found between populations as well as among the individual configurational areas. Although some ridge counts do not show familial resemblance, others appear to be moderately heritable. Estimates of h2 range from 0.36 to 0.63 in one family series and from 0.22 to 0.51 in the other. In addition, significant uterine environmental effects were detected in one family series but not in the other.     

Quantitative and genetic features of epidermal ridge minutiae on the palm of twins

The total minutia count (TMC) and fork index (FI), i.e., the proportion of forks in total minutiae, were examined in palm prints of 20 pairs each of monozygotic and dizygotic Japanese twins. No bilateral difference was found in either trait. The mean of the TMC was higher in males than in females, but the FI showed no sex difference. Both traits presented relatively high intraclass correlation coefficients between monozygotic twins, and genetic control of these traits is suggested. However, no correlation was observed between these two traits. A slight correlation was observed between the TMC and the total palmar interdigital ridge count. Some methodological problems concerned with classification criteria were discussed.     

Path analysis of palmar ridge counts.

The methods for path analysis of family resemblance (Rao et al., '74) are employed to test hypotheses concerning the inheritance of a-b, b-c and c-d palmar ridge counts using the correlation data of Pateria ('74). Homogeneity chi-square tests of the various familial correlations provide no evidence for sex-linkage of either kind, and also suggest that maternal effects are absent. The path coefficient model employed here involves heritability (additive) and common sibling environment. Variance components show that both heritability and common environment are significant, and account for most of the variation at each of the three ridge count area; b-c has the highest heritability, significantly higher than that for a-b or c-d.     

Fingerprint matching using the onion peeling approach and turning function

Fingerprint, as one of the most popular and robust biometric traits, can be used in automatic identification and verification systems to identify individuals. Fingerprint matching is a vital and challenging issue in fingerprint recognition systems. Most fingerprint matching algorithms are minutiae-based. The minutiae points are the ways that the fingerprint ridges can be discontinuous. Ridge ending and ridge bifurcation are two frequently used minutiae in most fingerprint matching algorithms. This article presents a new minutiae-based fingerprint matching using the onion peeling approach. In the proposed method, fingerprints are aligned to find the matched minutiae points. Then, the nested convex polygons of matched minutiae points are constructed and the comparison between peer-to-peer polygons is performed by the turning function distance. Simplicity, accuracy, and low time complexity of the onion peeling approach are three important factors that make it a standard method for fingerprint matching purposes. The performance of the proposed algorithm is evaluated on the database FVC2002. Since the fingerprints that the difference between the number of their layers is more than 2 and the a minutiae matching score lower than 0.15 are ignored, better results are obtained.KeywordsFingerprint Matching, Minutiae, Convex Layers, Turning Function, Computational Geometry.     

Estimation of the heritability of hair and eye color

In the present study the colours of hair are regarded as quantitative genetic characters. The genetic and environmental components of the total variance of the characters are determined by analysis of correlation between parents and children as well as full sibs. An analysis of correlation coefficients makes it possible to further examine whether autosomal dominance or X-linked factors play a role in the inheritance. The correlations between the parents make the genetical analysis more complicated as they raise the correlation coefficients between relatives. The estimates of heritability are 0.61 (hair-colour) and 0.80 (eye-colour). These estimates may serve as preliminary values of orientation. Only further studies will show whether the relative large part of the variance caused by the environment can be confirmed. Dominance may play a small role in the case of hair colour, while it seems to be absent in eye-colour. There are no sufficient indications of X-linked factors for both characters.     

Ridge course of the whorls: Classification and methods

In dermatoglyphic methodology the system of gross classification of digital pattern types needs modifications. More attention should be focussed on the study of minute morphological variations among pattern types in order to understand fully the genetic mechanisms involved in pattern variations. A systematic classification to record many of the morphological peculiarities is lacking. This paper proposes a classification and methods of identification of the direction of the course of the ridges inside the pattern area of true whorls. In all, nine ridge course types are identified, named and described. Data analysed on the basis of the above methods and classification reveal significant bilateral differences for clockwise and counter-clockwise types of ridge directions. Mode of inheritance, bisexual differences, etc., of the polymorphic course of these ridges should be studied. Its usefulness in the field of personal identification, population genetics and medicine should also be evaluated.     

Estimation of genetical parameters for a quantitative trait subject to major gene influences

Both regression and correlation estimates of genetical variance and heritability for a quantitative trait influenced by a major gene can be obtained from the error variance-covariance matrix of MANOVA using relative-relative phenotype pairs as factors. The method is illustrated with parent-offspring data on red cell acid phosphatase phenotypes and serum acid phosphatase activity.     

Birth wantedness reports: A look forward and a look back

Abstract

The majority of research indicates that estimates of heritability are not generalizable beyond the specific sample on which they have been calculated. This research has been limited, however, in its scope. The present set of investigations center upon an examination of previously reported heritability estimates for the scales of the Minnesota Multiphasic Personality Inventory (MMPI). The first investigation correlates the estimates for eight samples derived from a variety of published studies. The second investigation correlates the DZ twin pair and MZ twin pair intraclass correlations from four of the first investigation's samples. The third investigation correlates the estimates from one study in which the same sample was tested twice over a period of less than five years. It is concluded that no evidence is available for the generalizability of these estimates of MMPI scale heritability either across samples or even across time with the same sample.     

Heritability estimates for carcass traits of cattle: a review

We present estimates of heritability for carcass traits of cattle published in the scientific literature. Seventy-two papers published from 1962 to 2004, which reported estimates of heritability for carcass traits, were reviewed. The unweighted means of estimates of heritability for 14 carcass traits by slaughter end point (age, weight, and fat depth) were calculated. Among the three end points, carcass weight, backfat thickness, longissimus muscle area, and marbling score were the carcass traits with the most estimates of heritability (56 相似文献   

Multifactorial analysis of a mixed-longitudinal sample of Indian siblings: Age and sex effects on heritability

The aim of the present study was to examine the heritability of 11 traits in a mixed-longitudinal sample of Indian siblings, and to determine whether heritability estimates vary during the growth period and whether they are influenced by sex. The sample consisted of 245 brothers and 213 sisters from 138 nuclear families living in a semi-urban area in Kolkata, India. The age ranged between 5 and 19 years. The traits were standardised for age and sex using standard deviation scores (SDS) produced by the LMS method (Cole, T.J., 1988. Fitting smoothed centile curves to reference data. J. R. Stat. Soc. A 151, 385-418). The standard deviation scores were analysed by PCA. The two factors with eigenvalues above 1 explained 77.3% of the variance; they showed a high level of pleiotropism present among the studied traits and represented body lengths (PC1) and body weight and breadths (PC2). The heritability between all types of siblings (irrespective of sex) for the PC1 and PC2 was estimated. The heritability between various pairs of siblings showed variations along the whole ontogenetic period studied. During the childhood and pre-pubertal period, heritability between brothers, brother-sister pairs and any sibling pairs was mostly constant, with small and non-significant variations. All the pairs showed the lowest degree of heritability during puberty for PC1 but not for PC2, with significant changes of heritability estimates between adolescence and adulthood, in most of the analysed sibling pairs and in both PC factors. The highest heritability was generally observed at the end of the examined growth period in all pairs. A significant effect of sex on heritability was only detected for PC2 at 11 years of age.     

Dental development in the cotton ear marmoset (Callithrix jacchus)

The frequency of minutia types was studied in finger prints of 77 males and 82 females. Dermal ridges were clearly printed by a revised method for this purpose. The fork index, which represents the frequency of forks in minutiae, is higher in females for each finger than in males. It differs on each finger, i.e., low on the digit I, high on the digits, III, IV and V, and intermediate on the digit II. The mean of the index for each finger distributes from about 15 to 24. Bilateral difference is not evident. The correlation coefficient between right and left hands ranges from 0.52 to 0.79. Forks appear more frequently in ulnar loops than in whorls. It is revealed that the occurrence of forks differs in dermal regions.     

Variance,Inter-Trait Correlation,Heritability, and Marker-Trait Association of Rubber Yield-Related Characteristics in <Emphasis Type="Italic">Taraxacum kok-saghyz</Emphasis>

Rubber dandelion (Taraxacum kok-saghyz or TK) is a potential industrial crop species that can produce high-quality natural rubber in its roots. The present study estimated trait variance, inter-trait correlation, and entry-mean heritability for rubber yield-related traits and analyzed associations between these traits and 42 single-nucleotide polymorphism (SNP) markers. A trial was conducted at three environments to assess a biparental progeny of 66 F₁ full-sibs, in a randomized complete block design (RCBD) with two replicates. Significant correlations, broad ranges of variation, and significant genotypic variance components were identified for five measured phenotypic traits. Moderate broad-sense heritability on an entry-mean heritability estimates (0.51–0.61) were obtained for five rubber yield-related traits based on a 1-year trial. However, the broad-sense heritability in general sense ranged from 0.09 to 0.15 depending on the trait. Two linkage groups were identified. Association analysis identified seven significant marker-trait gene associations, and only one marker was related to two traits. The implications of trait correlations and heritability for selection and improvement are discussed.     

Familial aggregation of heart rate variability based on short recordings – the kibbutzim family study

The objective of this study was to assess the familial aggregation of heart rate variability (HRV), a readily measurable noninvasive reflection of cardiac autonomic function. Familial correlations were analyzed in 451 kibbutz members aged 15–97 years belonging to 80 kindreds. Five-minute duration Holter recordings made during silent supine spontaneous breathing and metronomic breathing were analyzed in the time and frequency domains. The present analysis considers the familial correlations and the heritability estimates of two time-domain indices, the standard deviation (SD) of the R-R interval (RR), reflecting total variability, and the root mean square of successive differences in RR intervals (RMSSD), reflecting vagal (parasympathetic) tone. During free breathing, age- and sex-adjusted correlations between parents and their children (r=0.24 for both indices) and between adult siblings above 30 years of age (r=0.24 and r=0.34 for SD and RMSSD, respectively) were statistically significant, whereas spouse correlations (r=–0.04, r=–0.02 for SD and RMSSD, respectively) and correlations in younger siblings (r=–0.22 and r=0.01, respectively) were not. Significant heritability estimates were demonstrated for the two indices (h ²=0.41 for SD and h ²=0.39 for RMSSD). These findings suggest that familial aggregation of HRV characteristics is determined mostly by genetic factors and less so by environmental factors and provide a basis for continuing the investigation into the underlying genetic influences on HRV. Received: 26 August 1997 / Accepted: 15 March 1998     

Family resemblance for serum uric acid in a Jerusalem sample of families

Summary Familial aggregation of serum uric acid was studied in a sample of families examined in the Jerusalem Lipid Research Clinic. We first examined homogeneity of familial correlations across the major origin groups in the Israeli population sample. In general correlations were homogeneous across origin groups, except for spouse pairs. Pooled correlations among biological relatives across the origin groups were all statistically significant. Spouse correlation upon adjustment for concomitant variables was moderately positive (r=0.115), yet significantly different from zero. Genetic and cultural determinants of uric acid were estimated utilizing a path model with 10 parameters to be estimated from a total of 16 correlations. Under a reduced model, genetic heritability (h²) was estimated to be 0.47±0.05 and cultural heritability (c²) was 0.11±0.03. However, our data gave suggestive evidence that cultural heritability was higher in parents (c²=0.28) than in children (c²=0.10). Commingling analysis and segregation analysis were also performed, and our findings imply that in the Israeli population there is no evidence for a major gene for high uric acid levels segregating in families.     

QUANTITATIVE GENETICS OF SEXUAL SIZE DIMORPHISM IN THE COLLARED FLYCATCHER,FICEDULA ALBICOLLIS

Quantitative genetic theory predicts that evolution of sexual size dimorphism (SSD) will be a slow process if the genetic correlation in size between the sexes is close to unity, and the heritability of size is similar in both sexes. However, there are very few reliable estimates of genetic correlations and sex-specific heritabilities from natural populations, the reasons for this being that (1) offspring have often been sexed retrospectively, and hence, selection acting differently with respect to body size in the two sexes between measuring and sex identification can bias estimates of SSD; and (2) in many taxa, parents may be incorrectly assigned to offspring either because of assignment errors or because of extrapair paternity. We used molecular sex and paternity identification to overcome these problems and estimated sex-specific heritabilities and the genetic correlation in body size between the two sexes in the collared flycatcher, Ficedula albicollis. After exclusion of the illegitimate offspring, the genetic correlation in body size between the sexes was 1.00 (SE = 0.22), implying a severe constraint on the evolution of SSD in this species. Furthermore, sex-specific heritability estimates were very similar, indicating that neither sex will be able to evolve faster than the other. By using estimated genetic parameters, together with empirically derived estimates of sex-specific selection gradients, we further demonstrated that the predicted selection response in female tarsus length is displaced about 200% in the opposite direction from that to be expected if there were no genetic correlation between the sexes. The correspondence between the biochemically estimated rate of extrapair paternity (about 15 % of the young) and that estimated from the “heritability method” (11%) was good. However, the estimated rate of extrapair paternity with the heritability method after exclusion of the illegitimate young was 22%, adding to increasing evidence that factors other than extrapair paternity (e.g., maternal effects) may be resposible for the commonly observed higher mother-offspring than father-offspring resemblance.     

Genetic epidemiology of multistage carcinogenesis

It is commonly believed that cancer is a multistage, polygenic disease. Even though conceptually appealing, the evidence supporting the multistage theory remains limited. Most known tumor suppresser genes are associated with monogenic dominant cancers following a two-hit pathway. We review results from a recent twin study on 90000 individuals that give support to the multistage theory. Statistically significant heritability estimates were shown for cancers of the colorectum (35%), breast (27%), and prostate (42%). These estimates are much higher than those obtained from family studies in which parents and offspring, or sibs are compared. The difference can be accounted for by the involvement of many genes. A polygenic cancer would show small effects in family studies but large effects in twin studies. We present calculations on the decrease in familial risks when the number of genes involved increases or when the penetrance decreases. We test the apparent number of stages involved in the main cancers from the Swedish Family-Cancer Database. The logarithms of the slopes suggest large differences in the apparent numbers of mutations involved in different cancers. The number of mutations required appears to be less in familial breast cancer compared to sporadic breast cancer. Study designs for gene identification should be revised to accommodate polygenic cancers.     

Genetic epidemiological study of blood pressure in a sedentary rural agricultural population of West Bengal, India

To study the genetic epidemiology of blood pressure (BP), data on 78 families were collected from a sedentary agricultural population of eastern India. The general levels of both systolic (SBP) and diastolic (DBP) blood pressures are found to be low (mean SBP = 106.41 mm Hg; mean DBP = 63.94 mm Hg). Trends of blood pressures with age are similar to those reported earlier (e.g., in the Framingham study). Environmental variables--e.g., occupation and tobacco use--do not have any direct significant effect on blood pressure variability in this population. Path analysis of family data shows a highly significant familial aggregation and yields a genetic heritability (maximum) estimate of 0.3 for both SBP and DBP. Sib-sib and mother-child correlation estimates are, respectively, 0.3 and 0.25. Father-child correlation estimates are 0.13 for SBP and near zero for DBP. A pseudopolygenic model yields the best fit to the data on SBP, while for DBP a proper resolution of various models considered could not be obtained.     

Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study

To examine the familial correlations, heritability (h ²) and common environmental components (c ²) of myopia and ocular biometric traits (all treated as continuous outcomes) in families collected through the Genes in Myopia (GEM) family study in Australia. A total of 132 pedigrees (723 participants) were recruited for this study. All individuals completed a risk factor questionnaire and underwent a detailed eye examination including spherical equivalent (SphE) and ocular biometric measurements of axial length (AL), anterior chamber depth (ACD) and corneal curvature (CC). Familial correlations were calculated and h ² and c² were estimated using a variance component model that assumes a multivariate t distribution within each pedigree. Two definitions of common environments (c ²) were considered: nuclear family (current) shared environment (Model 1) and sib-ship (childhood) shared environment (Model 2). Population ascertainment adjustment was performed using the Blue Mountains eye study dataset. The trends observed for familial correlations suggested that SphE is influenced by both environmental and genetic factors whereas AL, ACD and CC are predominantly genetically determined. This was largely confirmed by variance components modelling. Heritability estimates (adjusted for age, sex and years of education) from the best fitting ACE model (Model 2, childhood shared environment) were 0.50 ± 0.05 for SphE, 0.73 ± 0.04 for AL, 0.78 ± 0.04 for ACD and 0.16 ± 0.06 for CC. Childhood environmental effects were significant with c ² estimated to be 0.33 ± 0.04 for SphE, 0.06 ± 0.03 for AL, 0.22 ± 0.04 for ACD and 0.10 ± 0.05 for CC. Age was associated with SphE, total years of education was associated with AL and sex was associated with all traits studied. We used a novel and conservative approach to account for and estimate common environmental effects by specifying either nuclear family or sib-ship environment when estimating heritability estimates and showed that all traits examined (SphE, AL, ACD and CC) are heritable, thus reflecting a genetic component. These traits therefore all represent candidates for quantitative trait linkage analyses.