Effect of Crown Asymmetry on Size-Structure Dynamics of Plant Populations

The effect of crown asymmetry on the size–structure dynamicsof populations was evaluated using a spatial competition modelincorporating crown asymmetry. Computer simulations were carriedout with various combinations of density levels, spatial patterns,and degrees of asymmetry in competition to assess how they modifythe effect of crown asymmetry on size–structure dynamics. In the model, crown asymmetry is expressed by the crown-vector,or the vector linking the stem base and the centre of the projectedarea of the crown on the horizontal plane. Crown-vectors areassumed to develop in the manner by which crowns repel eachother. As crown-vectors develop, the positions of the crown-centresmove. Competition between individuals is expressed by a neighbourhoodmodel, in which individual growth is determined by the distancefrom, and size of, the neighbours' crown-centres. Generally, populations of individuals which developed asymmetriccrowns had larger survivorship, larger mean size, smaller coefficientsof variation and skewness, and a more regular spatial patternthan populations of individuals which developed symmetric crowns.The effect of crown symmetry is generally stronger in populationswith high density and a clumped spatial pattern. The effectof mortality caused by one-sided competition on size-structuredynamics was similar to that of crown asymmetry; mortality increasedmean size, reduced size hierarchy, and made the spatial patternmore regular. Because mortality was heavier in populations withoutcrown asymmetry, its effect on size-structure dynamics cancelledout, or overwhelmed, the effect of crown asymmetry in latergrowth stages. If crown asymmetry is associated with a reductionin growth, the effect of crown asymmetry is reduced. Nevertheless,the resultant population structure is different from that ofpopulations without crown asymmetry. Competition; crown asymmetry; morphological plasticity; neighbourhood interference model; size-structure dynamics     

Physical criteria of pathological processes. I. Change in the functional hemispheric asymmetry at various stages of rheumatic diseases]

The functional interhemispheric asymmetry of brain in patients with systemic rheumatic diseases was estimated by measuring brain direct current potentials. It is shown that different types of functional interhemispheric asymmetry correspond to different stages of systemic rheumatic diseases. At early stages, the left hemisphere asymmetry dominates, at expressed stages, the right hemisphere asymmetry is prevalent, and the terminal stage is characterized by the loss of functional interhemispheric asymmetry.     

Transbilayer coupling mechanism for the formation of lipid asymmetry in biological membranes. Application to the photoreceptor disc membrane.

An equilibrium transmembrane asymmetry in charged lipids is shown to arise as a result of oriented, bipolar proteins in the membrane. The basic interaction giving rise to the asymmetry is between a lipid molecule and a transbilayer potential generated by the asymmetric charge distribution in the protein. Thus, a protein can generate a lipid asymmetry without a direct binding interaction between lipid and protein. The generation of an asymmetry in charged lipid by this mechanism can also lead to a concomitant asymmetry in neutral lipids if deviations from ideality in the lipid mixture are taken into account. It is shown that regular solution theory applied to the lipid phase predicts an asymmetry in all components of a ternary mixture as long as one component is electrostatically oriented according to the mechanism mentioned above. The resulting asymmetry is not strongly salt dependent. The mechanism quantitatively accounts for the experimentally determined phospholipid asymmetry in the rod outer segment disc membrane of the vertebrate photoreceptor.     

Within-individual changes in developmental stability affect flight performance

Developmental stability, as measured by fluctuating asymmetry,has been purported to be an indicator of individual quality,and low asymmetry can be selected for by sexual selection processes.However, low asymmetry can also arise due to biomechanical constraintsoperating on trait design, as it is predicted that asymmetrywill decrease mechanical efficiency. Specifically, it has beenpredicted that wing length asymmetry will be negatively relatedto avian flight performance. To date, empirical investigationshave only studied the influence of increasing asymmetry beyondnaturally occurring average values. I examined the influenceof within-individual changes in primary feather developmentalstability on flight performance in European starlings by studyingasymmetry and flight before and after wing molt. Individualsthat exhibited a decrease in wing asymmetry through molt experiencedincreased aerodynamic performance in terms of both angle oftakeoff and level flapping-flight speed. Birds that increasedwing asymmetry suffered a decrease in flight performance. Takeoffspeed and the ability to negotiate an aerial obstacle coursewere unaffected by asymmetry. My data provide empirical supportfor the predicted influence of wing asymmetry on flight, eventhough the changes in asymmetry were very small (mean = 0.47%of trait size) and further indicate the importance of biomechanicalconsiderations in any study of developmental stability     

Dynamics of functional interhemisphere asymmetry and sexual dimorphism in rat ontogenesis

The dynamics of functional interhemispherical asymmetry in the ontogenesis of rats, males and females separately, was studied. The asymmetry was determined by the neurophysiological criterion, the interhemispherical gradient of the distribution of direct current potential of the brain. The sexual dimorphism upon age-related changes in the interhemispherical asymmetry was shown. It is assumed that this asymmetry is involved in the dynamics of neuroendocrine interactions determined by sex.     

Inbreeding reduces power-law scaling in the distribution of fluctuating asymmetry: an explanation of the basis of developmental instability

The study of fluctuating asymmetry has been controversial because of conflicting results found in much of the primary literature. It has been suggested that the source of this conflict is the fact that the basis of fluctuating asymmetry is poorly understood and that, as a consequence, methodology of fluctuating asymmetry studies may be flawed. A new model for the phenomenological basis of fluctuating asymmetry, that variation in fluctuating asymmetry is in large part due to the random exponential growth of cell populations (geometric Brownian motion) that are terminated randomly around a genetically programmed development time, is presented here. If termination of development has a genetic component, then scaling effects and kurtosis in the distribution of fluctuating asymmetry should increase with genetic redundancy of the population. This model prediction was tested by comparing the distribution of multivariate size and shape fluctuating asymmetry in large samples collected from both wild populations and four moderately inbred lines of Drosophila simulans. It was found that while wild populations were best described by a lognormal distribution with power-law scaled tails, the inbred lines derived from the wild stock were dramatically normalized (half-normal) in three of four cases. As predicted, the scaling exponent of the upper tail of the distribution of fluctuating asymmetry increased with inbreeding while the kurtosis and mean fluctuating asymmetry decreased with inbreeding. The model suggests an additional explanation of leptokurtosis in fluctuating asymmetry. Kurtosis and scaling of the statistical distribution of fluctuating asymmetry in a population is related directly to genetic differences between individuals and these differences affect their ability to buffer the process of development against random perturbations.     

Fluctuating and directional asymmetry in natural bird populations exposed to different levels of habitat disturbance, as revealed by mixture analysis

While bilateral trait asymmetry is widely recognized to estimate developmental instability, much controversy exists over which types of asymmetry (fluctuating, directional, and/or antisymmetry) to use. Recently it has been hypothesized that the three types are strongly interrelated, and that increased developmental instability may be reflected in a transition from fluctuating to directional asymmetry and/or antisymmetry. Alternatively, habitat disturbance might change the genetic expression of directional asymmetry. We present herein the first empirical evidence for stress-mediated shifts in types of asymmetry in natural populations, by using mixture analysis to model tarsus asymmetry in bird populations exposed to different levels of habitat disturbance. Observed asymmetry patterns almost exclusively consisted of true fluctuating asymmetry in the least disturbed populations, but became progressively mixed with directional asymmetry under increasing disturbance. Failing to unravel these mixtures of different forms of asymmetry may have critical implications for the analysis and interpretation of asymmetry data.     

Ectoparasites cause increased bilateral asymmetry of naturally selected traits in a colonial bird

Abstract Parasitism has been shown to correlate with levels of bilateral symmetry in some organisms, with more asymmetric individuals often having more parasites. However, few studies have shown experimentally that parasitism directly causes increased asymmetry. By fumigating some cliff swallow (Petrochelidon pyrrhonota) colonies and leaving others untreated, we investigated experimentally whether ectoparasitism by the cimicid swallow bug led to higher levels of asymmetry in length of wings, outer tail feathers, and tarsus among juvenile and adult birds. Juveniles from fumigated colonies measured soon after fledging had significantly less asymmetry in wing and outer tail length than juveniles from nonfumigated colonies; asymmetry in tarsus length was unaffected by parasitism. Adults that had undergone one or more post‐juvenal molts on the wintering grounds showed no differences in asymmetry between those reared in fumigated vs. nonfumigated colonies. These results show that ectoparasitism directly leads to increased feather asymmetry in cliff swallows, probably through parasite‐induced nutritional stress. Because wing and tail asymmetry impair flight performance and reduce foraging efficiency, the increased asymmetry caused by parasites represents a fitness cost to cliff swallows. This is among the few experimental studies to show an effect of parasites on asymmetry of naturally selected characters.     

Fluctuating asymmetry and inbreeding in Scandinavian gray wolves (Canis lupus)

We investigated fluctuating asymmetry in 13 traits of the skulls and jaws of historical and contemporary populations of Scandinavian gray wolves (Canis lupus). We hypothesized that there is a higher level of fluctuating asymmetry in the inbred contemporary population than in the historical population. Our analyses did not detect any difference in the level of fluctuating asymmetry as predicted. We propose different explanation for this lack of change in fluctuating asymmetry. It is assumed that a large number of studies have failed to find a positive correlation between the level of genetic stress and developmental instability and have therefore never been published, which hampers a good understanding of fluctuating asymmetry as an indicator of developmental instability. The current study is thus important in this context. The gray wolf population in Scandinavia is characterized by an extreme bottleneck followed by two and a half decades of strong inbreeding, but no associated change in fluctuating asymmetry is detected.     

Ectoparasitism in mothers causes higher positional fluctuating asymmetry in their sons: implications for sexual selection

Random deviations from perfect bilateral symmetry, fluctuating asymmetry, arise from developmental instability. I tested experimentally whether parasitism in female Drosophila nigrospiracula increases fluctuating asymmetry in male offspring. I also developed a novel measure for estimating developmental instability in a meristic trait called positional fluctuating asymmetry, which is based on the difference in the position of thoracic bristles between the right and left sternopleuron. I expected this measure to be a more sensitive indicator of developmental instability than the traditional numerical fluctuating asymmetry, because the latter is based on the difference in the actual presence or absence of bristles. Female flies burdened with hematophagous mites, Macrocheles subbadius (Macrochelidae), produced sons with significantly higher positional fluctuating asymmetry than did females carrying no mites. This effect, which may have resulted from impaired provisioning of oocytes by infested females, was dose dependent and magnified in the progeny of younger (18-20 d) versus older (30-32 d) females. This apparent magnification resulted from a slight but not significant increase in asymmetry of offspring of the older and unparasitized females. In contrast, the same mite loads had no effect on offspring numerical fluctuating asymmetry. If low-positional fluctuating asymmetry males enjoy a mating advantage, then with appropriate genetic variability, sexual selection could drive the evolution of host resistance in host populations. However, variability in neither kind of asymmetry influenced male mating success in nature. Thus, although male positional fluctuating asymmetry is causally associated with parasitism via maternal effects, asymmetry-based sexual selection is unlikely to influence the evolution of mite resistance in D. nigrospiracula. The value of the sensitivity afforded by positional fluctuating asymmetry is discussed in the context of sexual selection and conservation biology.     

Role of the hypophysis in fixing postural asymmetry at the segmental level in hemisection of the spinal cord

The role of the pituitary in the mechanisms of posttraumatic reorganizations of the segmental apparatus was studied. Hypophysectomized rats failed to demonstrate postural asymmetry after spinal cord hemisection. The lack of asymmetry is connected with a considerable decrease in postural asymmetry factor activity in the cerebrospinal fluid and cerebral tissue. It was established that pituitary tissue is characterized by the maximal level of postural asymmetry factor activity after hemisection.     

Sex and asymmetry in humans: what is the role of developmental instability?

Because asymmetric individuals are less attractive and may suffer from reduced fitness, bilateral asymmetry is widely believed to affect human sexual selection. Its evolutionary significance is based on the presumed relationship with developmental instability (DI). Yet, relationships between DI and bilateral asymmetry are often weak and possibly confounded by asymmetric mechanical loadings because of handedness. We related asymmetry in hands and faces to degrees of handedness and sexual behaviour in 100 humans. Handedness correlated to levels of asymmetry, thereby likely invalidating the use of asymmetry to estimate DI. For facial asymmetry, applying existing theoretical models refuted a link between asymmetry and DI. Explicit statistical modelling at the level of DI confirmed the absence of a link between DI and aspects of sexual behaviour. Nevertheless, asymmetries in both hands and face correlated significantly with sexual behaviour. We conclude that bilateral asymmetry per se, rather than its presumed link with DI, more likely relates to measures of human sexual behaviour. Because lateralization of behaviour appears widespread, evaluating the role of DI in evolution and ecology relies on a very critical selection of traits whose asymmetry can reliably reflect DI.     

Asymmetries of nature and the origin of biomolecular handedness

New developments in the problem of the origin of the asymmetry of the living systems are reviewed. The time of the appearance of the asymmetry was very probably during the chemical evolution. The asymmetry of weak interaction is still considered small to be the cause of chiral purity. New sources of asymmetry should also be considered, like the one proposed by Gilat.     

Left-right asymmetry in the alimentary canal of the Drosophila embryo

In many animal groups, left-right (LR) asymmetry within the body is observed. The left and right sides of the body are generally defined with reference to the anterior-posterior (AP) and dorsal-ventral (DV) axes. In this study, we investigated whether LR asymmetry is solely dependent on the AP and DV polarities in Drosophila embryos. We focused on the proventriculus, a posterior part of the foregut, and the hindgut because LR asymmetry in these body parts is highly stable in normal embryos. In embryos with a fully reversed AP polarity, LR asymmetry in both the proventriculus and the hindgut was re-oriented in relation to the reversed AP polarity. This demonstrates that inversion of AP polarity does not affect LR asymmetry of these tissues, and implies that LR asymmetry is specified in relation to the AP and DV polarities. Our findings were not consistent with the alternative hypothesis that LR asymmetry is predetermined by maternal signals that localize asymmetrically along the LR axis in the oocyte and/or early embryo.     

A measure of asymmetry of the skulls of odontocete whales

Linear measurements were made of the asymmetry of the skull which is characteristic of odontocete whales. Of the living genera (except Physeter, Tasmacetus, Stenella, Feresa and Lissodelphis) at least one specimen was measured; 317 skulls in all. One species, Stenodelphis blainvillei , proved symmetrical. All other species had leftward deviation of the nasal prominence. No specimen showed inverse asymmetry.
When, for species or families, regressions were formed of the asymmetry measure on skull length the slopes formed a sequence such that Kogia >monodontids>delphinoids (except Orcinus)>ziphiids> Orcinus. In some species of delphinoid, in the delphinoids as a group, and more strongly in Monodon , the proportion of asymmetry to skull length increased with increasing size. In the ziphiids, as a family, asymmetry increased roughly linearly with bodily size. Orcinus orca proved an anomalous delphinoid in having little asymmetry for its size. The asymmetry of the skull of Monodon monoceros is independent of the possession of a tusk.
It is suggested that the leftward deviation of the dorsal aspect of the skull acts to conserve the symmetry of the body surface by countering an opposite asymmetry of the upper breathing passages, an asymmetry which is primary but whose function is unknown.     

Bilateral asymmetry of the humerus during growth and development

The development of handedness throughout growth can be investigated by using bilateral asymmetry of the humerus as a proxy for this trait. A large skeletal sample of nonadults from English archaeological sites was examined using standard metric techniques to assess when right-sided asymmetry first appears in the human skeleton. Results of this work indicate a change in directional asymmetry during growth and development, with infants and young children exhibiting no significant asymmetry and older children and adolescents demonstrating right-sidedness. This trend is consistent with what has been observed in previous studies of upper limb asymmetry in skeletal material and behaviorally in living children, adding further strength to the premise that biomechanical forces strongly influence bilateral asymmetry in the upper limb bones. Variability in the magnitude of asymmetry between different features of the humerus was also noted. This characteristic can be explained by differing degrees of genetic canalization, with length and articular dimensions being more strongly canalized than diaphyseal properties.     

GEOMETRIC MORPHOMETRICS OF DEVELOPMENTAL INSTABILITY: ANALYZING PATTERNS OF FLUCTUATING ASYMMETRY WITH PROCRUSTES METHODS

Although fluctuating asymmetry has become popular as a measure of developmental instability, few studies have examined its developmental basis. We propose an approach to investigate the role of development for morphological asymmetry by means of morphometric methods. Our approach combines geometric morphometrics with the two-way ANOVA customary for conventional analyses of fluctuating asymmetry and can discover localized features of shape variation by examining the patterns of covariance among landmarks. This approach extends the notion of form used in studies of fluctuating asymmetry from collections of distances between morphological landmarks to an explicitly geometric concept of shape characterized by the configuration of landmarks. We demonstrate this approach with a study of asymmetry in the wings of tsetse flies (Glossina palpalis gambiensis). The analysis revealed significant fluctuating and directional asymmetry for shape as well as ample shape variation among individuals and between the offspring of young and old females. The morphological landmarks differed markedly in their degree of variability but multivariate patterns of landmark covariation identified by principal component analysis were generally similar between fluctuating asymmetry (within-individual variability) and variation among individuals. Therefore there is no evidence that special developmental processes control fluctuating asymmetry. We relate some of the morphometric patterns to processes known to be involved in the development of fly wings.     

Origins of asymmetry in the CNS

Vertebrate ancestors had extreme asymmetry of the CNS, largely imposed by bodily asymmetry. In the zebrafish a key asymmetry is that of the habenulae. Their major outflow on the left is concerned with visual control of sustained response to targets, and on the right with response to potent releasers of innate responses. Mammals retain comparable outflows but without obvious asymmetry. Behavioural asymmetries associated with the processing of perceptual information are, if anything, exaggerated. Evidence from insects suggests that these latter asymmetries are of great value in any complex CNS. Bodily asymmetry may therefore not be essential for their evolution.     

Gating currents in th intact crayfish giant axon.

Both single-sweep and signal-averaged asymmetry current are measured from intact crayfish axons after ionic currents are blocked with tetrodotoxin and 4-aminopyridine. The ON asymmetry charge saturates at about 0 mV and no ON charge movement is detectable at voltages negative to -140 mV. The areas of ON and OFF asymmetry charge are equal for short depolarizations but the ratio QOFF/QON decreases for longer depolarizing pulses. Sodium and asymmetry current magnitudes can be changed in parallel by lowering the hold potential or by imposing conditioning prepulses. Our results are consistent with the concept that asymmetry current in generated by movement of trapped charge in association with Na channel gating.     

The ins and outs of phospholipid asymmetry in the plasma membrane: roles in health and disease

A common feature of all eukaryotic membranes is the non-random distribution of different lipid species in the lipid bilayer (lipid asymmetry). Lipid asymmetry provides the two sides of the plasma membrane with different biophysical properties and influences numerous cellular functions. Alteration of lipid asymmetry plays a prominent role during cell fusion, activation of the coagulation cascade, and recognition and removal of apoptotic cell corpses by macrophages (programmed cell clearance). Here we discuss the origin and maintenance of phospholipid asymmetry, based on recent studies in mammalian systems as well as in Caenhorhabditis elegans and other model organisms, along with emerging evidence for a conserved role of mitochondria in the loss of lipid asymmetry during apoptosis. The functional significance of lipid asymmetry and its disruption during health and disease is also discussed.