Size

Distribution by Scientific Domains
Distribution within Life Sciences

Kinds of Size

  • abnormal size
  • absolute size
  • actual size
  • adequate sample size
  • adipocyte size
  • adult body size
  • adult size
  • aggregate size
  • allele size
  • ancestral size
  • angular size
  • antenna size
  • antler size
  • appropriate size
  • approximate size
  • arbitrary size
  • area size
  • array size
  • artery size
  • asymptotic size
  • atrial size
  • average body size
  • average cell size
  • average crystallite size
  • average grain size
  • average particle size
  • average pore size
  • average size
  • badge size
  • bank size
  • basin size
  • batch size
  • bead size
  • beam size
  • birth size
  • block size
  • board size
  • body size
  • bone size
  • brain size
  • brood size
  • bubble size
  • burst size
  • business size
  • calculating sample size
  • canopy size
  • cardiac size
  • catchment size
  • catheter size
  • cavity size
  • cell size
  • census population size
  • census size
  • centroid size
  • certain size
  • characteristic size
  • chip size
  • chromosome size
  • city size
  • class size
  • cluster size
  • clutch size
  • cohort size
  • colony size
  • community size
  • compact size
  • company size
  • comparable size
  • constant size
  • controllable pore size
  • controllable size
  • core size
  • crack size
  • cranial size
  • critical size
  • crop size
  • crown size
  • crystal size
  • crystallite size
  • cup size
  • current population size
  • current size
  • decreased size
  • decreasing particle size
  • defect size
  • device size
  • diameter size
  • different body size
  • different mesh size
  • different particle size
  • different population size
  • different pore size
  • different size
  • disc size
  • display size
  • domain size
  • drop size
  • droplet size
  • effect size
  • effective population size
  • effective size
  • egg size
  • electrode size
  • element size
  • embryo size
  • ensemble size
  • equal size
  • equivalent size
  • estimating population size
  • event size
  • expected sample size
  • expected size
  • eye size
  • family size
  • farm size
  • feature size
  • female body size
  • female size
  • fiber size
  • fibre size
  • field size
  • file size
  • filler size
  • filter size
  • final size
  • fine grain size
  • finite size
  • firm size
  • fish size
  • floc size
  • follicle size
  • fragment size
  • fruit size
  • full size
  • gall size
  • gap size
  • genome size
  • geographic range size
  • geographical range size
  • geometric size
  • gift size
  • gland size
  • government size
  • graft size
  • grain size
  • granule size
  • greater size
  • grid cell size
  • grid size
  • group size
  • habitat size
  • harem size
  • hatchling size
  • head size
  • heart size
  • herd size
  • hole size
  • home range size
  • home-range size
  • horn size
  • hospital size
  • host size
  • household size
  • hydrodynamic size
  • identical size
  • image size
  • increased cell size
  • increased population size
  • increased size
  • increasing body size
  • increasing fish size
  • increasing population size
  • increasing size
  • individual size
  • inflorescence size
  • initial particle size
  • initial size
  • inoculum size
  • insert size
  • insufficient sample size
  • intermediate size
  • island size
  • juvenile size
  • kernel size
  • la size
  • lake size
  • large body size
  • large colony size
  • large effect size
  • large grain size
  • large male size
  • large population size
  • large sample size
  • large size
  • large tumor size
  • large tumour size
  • larger body size
  • larger particle size
  • larger pore size
  • larger sample size
  • larger size
  • larger tumor size
  • larval size
  • lateral size
  • leaf size
  • leave atrial size
  • lesion size
  • limited sample size
  • limited size
  • linear size
  • litter size
  • liver size
  • load size
  • local population size
  • long-term effective population size
  • lot size
  • lymph node size
  • male body size
  • male size
  • mandible size
  • market size
  • marketable size
  • mass size
  • maternal size
  • maximal size
  • maximum body size
  • maximum size
  • meal size
  • mean body size
  • mean clutch size
  • mean effect size
  • mean grain size
  • mean litter size
  • mean particle size
  • mean size
  • mean tumor size
  • median size
  • median tumor size
  • median tumour size
  • medium effect size
  • medium size
  • membrane pore size
  • mesh size
  • mi size
  • micellar size
  • minimum size
  • minimum viable population size
  • model size
  • moderate size
  • molecular size
  • muscle fibre size
  • muscle size
  • nanometer size
  • nanometric size
  • nanoparticle size
  • neighbourhood size
  • nest size
  • network size
  • nm size
  • node size
  • normal size
  • nuclear size
  • offspring body size
  • offspring size
  • one size
  • optimal body size
  • optimal size
  • optimum size
  • organ size
  • organization size
  • organizational size
  • original size
  • ovary size
  • pack size
  • panel size
  • particle size
  • patch size
  • pelvic size
  • physical size
  • pixel size
  • placental size
  • plant population size
  • plant size
  • plaque size
  • plasmid size
  • pollen size
  • polymer size
  • polyp size
  • pond size
  • pool size
  • population size
  • pore size
  • portion size
  • potential size
  • predator size
  • predicted size
  • prey body size
  • prey size
  • primary particle size
  • probe size
  • problem size
  • prostate size
  • protein size
  • pupil size
  • range size
  • reactor size
  • reduced size
  • relative brain size
  • relative size
  • remnant size
  • repeat size
  • repertoire size
  • reproductive size
  • required sample size
  • ring size
  • run size
  • same size
  • sample size
  • school size
  • sediment grain size
  • seed size
  • seedling size
  • set size
  • sheath size
  • sheer size
  • sibship size
  • similar body size
  • similar size
  • site size
  • skeletal muscle size
  • skeletal size
  • small body size
  • small cell size
  • small effect size
  • small effective population size
  • small grain size
  • small particle size
  • small population size
  • small sample size
  • small size
  • smaller body size
  • smaller effect size
  • smaller grain size
  • smaller particle size
  • smaller pore size
  • smaller sample size
  • smaller size
  • smallest sample size
  • social group size
  • soma size
  • species pool size
  • species range size
  • species size
  • specific size
  • specimen size
  • sperm size
  • spine size
  • spleen size
  • spot size
  • stent size
  • step size
  • stimulus size
  • stock size
  • stone size
  • stream size
  • structural size
  • study size
  • substratum size
  • sufficient size
  • suitable size
  • support size
  • system size
  • tank size
  • target size
  • territory size
  • testicular size
  • testis size
  • thymic size
  • thymus size
  • tick size
  • time step size
  • time-step size
  • tooth size
  • total population size
  • total sample size
  • total size
  • trade size
  • trait size
  • treatment effect size
  • tree size
  • true size
  • trunk size
  • tube size
  • tumor size
  • tumour size
  • tunable size
  • ulcer size
  • uniform size
  • unit size
  • urban size
  • variable size
  • variance effective size
  • various size
  • varying size
  • ventricle size
  • ventricular size
  • very large sample size
  • very small size
  • vessel size
  • viable population size
  • vocabulary size
  • voxel size
  • waist size
  • wheal size
  • window size
  • wing size
  • zone size

  • Terms modified by Size

  • size advantage
  • size alone
  • size analysis
  • size analyzer
  • size calculation
  • size category
  • size change
  • size characteristic
  • size class
  • size class distribution
  • size cline
  • size close
  • size composition
  • size constraint
  • size control
  • size data
  • size decrease
  • size decreased
  • size defect
  • size dependence
  • size dependency
  • size dependent
  • size determination
  • size difference
  • size differentiation
  • size dimorphism
  • size discrimination
  • size distortion
  • size distribution
  • size effect
  • size effects
  • size estimate
  • size estimation
  • size evolution
  • size exclusion
  • size exclusion chromatography
  • size formula
  • size fraction
  • size frequency
  • size frequency distribution
  • size gradient
  • size greater
  • size group
  • size groups
  • size heterogeneity
  • size hierarchy
  • size increase
  • size index
  • size inequality
  • size larger
  • size limit
  • size manipulation
  • size marker
  • size matter
  • size measurement
  • size n
  • size parameter
  • size pattern
  • size problem
  • size range
  • size ratio
  • size reduction
  • size refuge
  • size regulation
  • size relationships
  • size requirement
  • size scale
  • size selection
  • size selectivity
  • size shows
  • size smaller
  • size spectrum
  • size structure
  • size suitable
  • size threshold
  • size trait
  • size used
  • size v
  • size value
  • size variability
  • size variation

  • Selected Abstracts


    SIZE OF HOUSEHOLD FIREARM COLLECTIONS: IMPLICATIONS FOR SUBCULTURES AND GENDER,

    CRIMINOLOGY, Issue 3 2007
    BRIAN R. WYANT
    Recent work (Cook and Ludwig, 2003) has linked local firearm density to increased burglary victimization risk. The current work investigates within-household gun density or household firearm collection size. Previous work has suggested two subcultures of gun owners: protection-minded and sport- or hunting-minded. It also has identified gender gaps in reporting any household guns and in the number reported. None of the earlier work, however, has controlled for selection into gun-owning household status. This limitation raises potential questions about earlier findings. The current research controls for selection. If the two subcultures thesis is correct, protection-minded owners should report smaller household firearm collections. The expected impact is observed in one national survey and is partially replicated in a second. Gender gaps seemed more independent than previously suggested. This study is the first to provide evidence of two partially overlapping subcultures of gun owners even after controlling for selection into gun-owning household status. Practical implications for burglary risk may exist. [source]


    SHOULD AUSTRALIA TARGET ITS POPULATION SIZE?

    ECONOMIC PAPERS: A JOURNAL OF APPLIED ECONOMICS AND POLICY, Issue 1 2003
    HARRY CLARKE
    First page of article [source]


    EXTREME SELECTION ON SIZE IN THE EARLY LIVES OF FISH

    EVOLUTION, Issue 8 2010
    Kestrel O. Perez
    Although fitness typically increases with body size and selection gradients on size are generally positive, much of this information comes from terrestrial taxa. In the early life history of fish, there is evidence of selection both for and against larger size, leaving open the question of whether the general pattern for terrestrial taxa is valid for fish. We reviewed studies of size-dependent survival in the early life history of fish and obtained estimates of standardized selection differentials from 40 studies. We found that 77% of estimated selection differentials favored larger size and that the strength of selection was more than five times that seen in terrestrial taxa. Selection decreased with study period duration and initial length, and disruptive selection occurred significantly more frequently than stabilizing selection. Contrary to expectations from Bergmann's rule, selection on size did not increase with latitude. [source]


    EVOLUTION OF SCAPULA SIZE AND SHAPE IN DIDELPHID MARSUPIALS (DIDELPHIMORPHIA: DIDELPHIDAE)

    EVOLUTION, Issue 9 2009
    Diego Astúa
    The New World family Didelphidae, the basal lineage within marsupials, is commonly viewed as morphologically conservative, yet includes aquatic, terrestrial, scansorial, and arboreal species. Here, I quantitatively estimated the existing variability in size and shape of the Didelphidae scapula (1076 specimens from 56 species) using geometric morphometrics, and compared size and shape differences to evolutionary and ecologic distances. I found considerable variation in the scapula morphology, most of it related to size differences between species. This results in morphologic divergence between different locomotor habits in larger species (resulting from increased mechanical loads), but most smaller species present similarly shaped scapulae. The only exceptions are the water opossum and the short-tailed opossums, and the functional explanations for these differences remain unclear. Scapula size and shape were mapped onto a molecular phylogeny for 32 selected taxa and ancestral size and shapes were reconstructed using squared-changed parsimony. Results indicate that the Didelphidae evolved from a medium- to small-sized ancestor with a generalized scapula, slightly more similar to arboreal ones, but strikingly different from big-bodied present arboreal species, suggesting that the ancestral Didelphidae was a small scansorial animal with no particular adaptations for arboreal or terrestrial habits, and these specializations evolved only in larger-bodied clades. [source]


    A TEST AND REVIEW OF THE ROLE OF EFFECTIVE POPULATION SIZE ON EXPERIMENTAL SEXUAL SELECTION PATTERNS

    EVOLUTION, Issue 7 2009
    Rhonda R. Snook
    Experimental evolution, particularly experimental sexual selection in which sexual selection strength is manipulated by altering the mating system, is an increasingly popular method for testing evolutionary theory. Concerns have arisen regarding genetic diversity variation across experimental treatments: differences in the number and sex ratio of breeders (effective population size; Ne) and the potential for genetic hitchhiking, both of which may cause different levels of genetic variation between treatments. Such differences may affect the selection response and confound interpretation of results. Here we use both census-based estimators and molecular marker-based estimates to empirically test how experimental evolution of sexual selection in Drosophila pseudoobscura impacts Ne and autosomal genetic diversity. We also consider effects of treatment on X-linked Nes, which have previously been ignored. Molecular autosomal marker-based estimators indicate that neither Ne nor genetic diversity differs between treatments experiencing different sexual selection intensities; thus observed evolutionary responses reflect selection rather than any confounding effects of experimental design. Given the increasing number of studies on experimental sexual selection, we also review the census Nes of other experimental systems, calculate X-linked Ne, and compare how different studies have dealt with the issues of inbreeding, genetic drift, and genetic hitchhiking to help inform future designs. [source]


    RELATIVE CONTRIBUTION OF ADDITIVE, DOMINANCE, AND IMPRINTING EFFECTS TO PHENOTYPIC VARIATION IN BODY SIZE AND GROWTH BETWEEN DIVERGENT SELECTION LINES OF MICE

    EVOLUTION, Issue 5 2009
    Reinmar Hager
    Epigenetic effects attributed to genomic imprinting are increasingly recognized as an important source of variation in quantitative traits. However, little is known about their relative contribution to phenotypic variation compared to those of additive and dominance effects, and almost nothing about their role in phenotypic evolution. Here we address these questions by investigating the relative contribution of additive, dominance, and imprinting effects of quantitative trait loci (QTL) to variation in "early" and "late" body weight in an intercross of mice selected for divergent adult body weight. We identified 18 loci on 13 chromosomes; additive effects accounted for most of the phenotypic variation throughout development, and imprinting effects were always small. Genetic effects on early weight showed more dominance, less additive, and, surprisingly, less imprinting variation than that of late weight. The predominance of additivity of QTL effects on body weight follows the expectation that additive effects account for the evolutionary divergence between selection lines. We hypothesize that the appearance of more imprinting effects on late body weight may be a consequence of divergent selection on adult body weight, which may have indirectly selected for alleles showing partial imprinting effects due to their associated additive effects, highlighting a potential role of genomic imprinting in the response to selection. [source]


    DOES VARIATION IN SELECTION IMPOSED BY BEARS DRIVE DIVERGENCE AMONG POPULATIONS IN THE SIZE AND SHAPE OF SOCKEYE SALMON?

    EVOLUTION, Issue 5 2009
    Stephanie M. Carlson
    Few studies have determined whether formal estimates of selection explain patterns of trait divergence among populations, yet this is one approach for evaluating whether the populations are in equilibria. If adaptive divergence is complete, directional selection should be absent and stabilizing selection should prevail. We estimated natural selection, due to bear predation, acting on the body size and shape of male salmon in three breeding populations that experience differing predation regimes. Our approach was to (1) estimate selection acting within each population on each trait based on an empirical estimate of reproductive activity, (2) test for trait divergence among populations, and (3) test whether selection coefficients were correlated with trait divergence among populations. Stabilizing selection was never significant, indicating that these populations have yet to attain equilibria. Directional selection varied among populations in a manner consistent with trait divergence, indicating ongoing population differentiation. Specifically, the rank order of the creeks in terms of patterns of selection paralleled the rank order in terms of size and shape. The shortest and least deep-bodied males had the highest reproductive activity in the creek with the most intense predation and longer and deeper-bodied males were favored in the creeks with lower predation risk. [source]


    A SELECTION MODEL OF MOLECULAR EVOLUTION INCORPORATING THE EFFECTIVE POPULATION SIZE

    EVOLUTION, Issue 2 2009
    Hans Ellegren
    First page of article [source]


    ON THE ADAPTIVE ACCURACY OF DIRECTIONAL ASYMMETRY IN INSECT WING SIZE

    EVOLUTION, Issue 11 2008
    Christophe Pélabon
    Subtle left,right biases are often observed in organisms with an overall bilateral symmetry. The evolutionary significance of these directional asymmetries remains uncertain, however, and scenarios of both developmental constraints and adaptation have been suggested. Reviewing the literature on asymmetry in insect wings, we analyze patterns of directional asymmetry in wing size to evaluate the possible adaptive significance of this character. We found that directional asymmetry in wing size is widespread among insects, with left- and right-biased asymmetries commonly observed. The direction of the asymmetry does not appear to be evolutionarily conserved above the species level. Overall, we argue that the very small magnitude of directional asymmetry, 0.7% of the wing size on average, associated with an extremely imprecise expression, precludes directional asymmetry from playing any major adaptive role. [source]


    EVOLUTIONARY REDUCTION IN TESTES SIZE AND COMPETITIVE FERTILIZATION SUCCESS IN RESPONSE TO THE EXPERIMENTAL REMOVAL OF SEXUAL SELECTION IN DUNG BEETLES

    EVOLUTION, Issue 10 2008
    Leigh W. Simmons
    Sexual selection is thought to favor the evolution of secondary sexual traits in males that contribute to mating success. In species where females mate with more than one male, sexual selection also continues after copulation in the form of sperm competition and cryptic female choice. Theory suggests that sperm competition should favor traits such as testes size and sperm production that increase a male's competitive fertilization success. Studies of experimental evolution offer a powerful approach for assessing evolutionary responses to variation in sexual selection pressures. Here we removed sexual selection by enforcing monogamy on replicate lines of a naturally polygamous horned beetle, Onthophagus taurus, and monitoring male investment in their testes for 21 generations. Testes size decreased in monogamous lines relative to lines in which sexual selection was allowed to continue. Differences in testes size were dependent on selection history and not breeding regime. Males from polygamous lines also had a competitive fertilization advantage when in sperm competition with males from monogamous lines. Females from polygamous lines produced sons in better condition, and those from monogamous lines increased their sons condition by mating polygamously. Rather than being costly for females, multiple mating appears to provide females with direct and/or indirect benefits. Neither body size nor horn size diverged between our monogamous and polygamous lines. Our data show that sperm competition does drive the evolution of testes size in onthophagine beetles, and provide general support for sperm competition theory. [source]


    EFFECTS OF POLLEN LOAD SIZE ON SEED PATERNITY IN WILD RADISH: THE ROLES OF POLLEN COMPETITION AND MATE CHOICE

    EVOLUTION, Issue 8 2007
    Diane L. Marshall
    For sexual selection to be important in plants, it must occur at pollen load sizes typical of field populations. However, studies of the impact of pollen load size on pollen competition have given mixed results, perhaps because so few of these studies directly examined the outcome of mating when pollen load size was varied. We asked whether seed paternity after mixed pollination of wild radish was affected by pollen load sizes ranging from 22 to 220 pollen grains per stigma. We examined the seed siring abilities of 12 pollen donors across 11 maternal plants. Seed paternity was statistically indistinguishable across the pollen load sizes even though, overall, the pollen donors sired different numbers of seeds. This lack of effect of pollen load size on seed paternity may have occurred because fruit abortion and early abortion or failure of fertilization of seeds increased as load size decreased. Thus, failures of fruits and seeds sired by poorer pollen donors may keep seed paternity constant across pollen load sizes. [source]


    CROSS-GENERATIONAL ENVIRONMENTAL EFFECTS AND THE EVOLUTION OF OFFSPRING SIZE IN THE TRINIDADIAN GUPPY POECILIA RETICULATA

    EVOLUTION, Issue 2 2006
    Farrah Bashey
    Abstract The existence of adaptive phenotypic plasticity demands that we study the evolution of reaction norms, rather than just the evolution of fixed traits. This approach requires the examination of functional relationships among traits not only in a single environment but across environments and between traits and plasticity itself. In this study, I examined the interplay of plasticity and local adaptation of offspring size in the Trinidadian guppy, Poecilia reticulata. Guppies respond to food restriction by growing and reproducing less but also by producing larger offspring. This plastic difference in offspring size is of the same order of magnitude as evolved genetic differences among populations. Larger offspring sizes are thought to have evolved as an adaptation to the competitive environment faced by newborn guppies in some environments. If plastic responses to maternal food limitation can achieve the same fitness benefit, then why has guppy offspring size evolved at all? To explore this question, I examined the plastic response to food level of females from two natural populations that experience different selective environments. My goals were to examine whether the plastic responses to food level varied between populations, test the consequences of maternal manipulation of offspring size for offspring fitness, and assess whether costs of plasticity exist that could account for the evolution of mean offspring size across populations. In each population, full-sib sisters were exposed to either a low- or high-food treatment. Females from both populations produced larger, leaner offspring in response to food limitation. However, the population that was thought to have a history of selection for larger offspring was less plastic in its investment per offspring in response to maternal mass, maternal food level, and fecundity than the population under selection for small offspring size. To test the consequences of maternal manipulation of offspring size for offspring fitness, I raised the offspring of low- and high-food mothers in either low- or high-food environments. No maternal effects were detected at high food levels, supporting the prediction that mothers should increase fecundity rather than offspring size in noncompetitive environments. For offspring raised under low food levels, maternal effects on juvenile size and male size at maturity varied significantly between populations, reflecting their initial differences in maternal manipulation of offspring size; nevertheless, in both populations, increased investment per offspring increased offspring fitness. Several correlates of plasticity in investment per offspring that could affect the evolution of offspring size in guppies were identified. Under low-food conditions, mothers from more plastic families invested more in future reproduction and less in their own soma. Similarly, offspring from more plastic families were smaller as juveniles and female offspring reproduced earlier. These correlations suggest that a fixed, high level of investment per offspring might be favored over a plastic response in a chronically low-resource environment or in an environment that selects for lower reproductive effort [source]


    DOES LARGE BODY SIZE IN MALES EVOLVE TO FACILITATE FORCIBLE INSEMINATION?

    EVOLUTION, Issue 11 2005
    A STUDY ON GARTER SNAKES
    Abstract A trend for larger males to obtain a disproportionately high number of matings, as occurs in many animal populations, typically is attributed either to female choice or success in male-male rivalry; an alternative mechanism, that larger males are better able to coercively inseminate females, has received much less attention. For example, previous studies on garter snakes (Thamnophis sirtalis parietalis) at communal dens in Manitoba have shown that the mating benefit to larger body size in males is due to size-dependent advantages in male-male rivalry. However, this previous work ignored the possibility that larger males may obtain more matings because of male-female interactions. In staged trials within outdoor arenas, larger body size enhanced male mating success regardless of whether a rival male was present. The mechanism involved was coercion rather than female choice, because mating occurred most often (and soonest) in females that were least able to resist courtship-induced hypoxic stress. Males do physically displace rivals from optimal positions in the mating ball, and larger males are better able to resist such displacement. Nonetheless, larger body size enhances male mating success even in the absence of such malemale interactions. Thus, even in mating systems where males compete physically and where larger body size confers a significant advantage in male-male competition, the actual selective force for larger body size in males may relate to forcible insemination of unreceptive females. Experimental studies are needed to determine whether the same situation occurs in other organisms in which body-size advantages have been attributed to male-male rather than male-female interactions. [source]


    THE EFFECT OF SELF-FERTILIZATION, INBREEDING DEPRESSION, AND POPULATION SIZE ON AUTOPOLYPLOID ESTABLISHMEN

    EVOLUTION, Issue 9 2005
    Joseph H. Rausch
    Abstract The minority cytotype exclusion principle describes how random mating between diploid and autotetraploid cytotypes hinders establishment of the rare cytotype. We present deterministic and stochastic models to ascertain how selfing, inbreeding depression, unreduced gamete production, and finite population size affect minority cytotype exclusion and the establishment of autotetraploids. Results demonstrate that higher selfing rates and lower inbreeding depression in autotetraploids facilitate establishment of autotetraploid populations. Stochastic effects due to finite population size increase the probability of polyploid establishment and decrease the mean time to tetraploid fixation. Our results extend the minority cytotype exclusion principle to include important features of plant reproduction and demonstrate that variation in mating system parameters significantly influences the conditions necessary for polyploid establishment. [source]


    HETEROZYGOTE EXCESS IN SMALL POPULATIONS AND THE HETEROZYGOTE-EXCESS EFFECTIVE POPULATION SIZE

    EVOLUTION, Issue 9 2004
    Franclois Balloux
    Abstract It has been proposed that effective size could be estimated in small dioecious population by considering the heterozygote excess observed at neutral markers. When the number of breeders is small, allelic frequencies in males and females will slightly differ due to binomial sampling error. However, this excess of heterozygotes is not generated by dioecy but by the absence of individuals produced through selfing. Consequently, the approach can also be applied to self-incompatible monoecious species. Some inaccuracies in earlier equations expressing effective size as function of the heterozygote excess are also corrected in this paper. The approach is then extended to subdivided populations, where time of sampling becomes crucial. When adults are sampled, the effective size of the entire population can be estimated, whereas when juveniles are sampled, the average effective number of breeders per subpopulations can be estimated. The main limitation of the heterozygote excess method is that it will only perform satisfactorily for populations with a small number of reproducing individuals. While this situation is unlikely to happen frequently at the scale of the entire population, structured populations with small subpopulations are likely to be common. The estimation of the average number of breeders per subpopulations is thus expected to be applicable to many natural populations. The approach is straightforward to compute and independent of equilibrium assumptions. Applications to simulated data suggest the estimation of the number of breeders to be robust to mutation and migration rates, and to specificities of the mating system. [source]


    CONDITION DEPENDENCE OF SEXUAL ORNAMENT SIZE AND VARIATION IN THE STALK-EYED FLY CYRTODIOPSIS DALMANNI (DIPTERA: DIOPSIDAE)

    EVOLUTION, Issue 5 2004
    Samuel Cotton
    Abstract We used the stalk-eyed fly Cyrtodiopsis dalmanni to examine predictions made by condition-dependent handicap models of sexual selection. Condition was experimentally varied by manipulation of larval food availability. Cyrtodiopsis dalmanni is a highly dimorphic species exhibiting strong sexual selection, and the male sexual ornament (exaggerated eyespan) showed strong condition-dependent expression relative to the homologous trait in females and nonsexual traits. Male eyespan also showed a great increase in standardized variance under stress, unlike nonsexual traits. The inflated variance of the male ornament was primarily attributable to condition-dependent (but body-size-independent) increase in variance. Thus, evaluation of male eyespan allows females to gain additional information about male condition over and above that given by body size. These findings accord well with condition-dependent handicap models of sexual selection. [source]


    DIFFERENT CELL SIZE AND CELL NUMBER CONTRIBUTION IN TWO NEWLY ESTABLISHED AND ONE ANCIENT BODY SIZE CLINE OF DROSOPHILA SUBOBSCURA

    EVOLUTION, Issue 3 2003
    Federico C. F. Calboli
    Abstract Latitudinal genetic clines in body size occur in many ectotherms including Drosophila species. In the wing of D. melanogaster, these clines are generally based on latitudinal variation in cell number. In contrast, differences in wing area that evolve by thermal selection in the laboratory are in general based on cell size. To investigate possible reasons for the different cellular bases of these two types of evolutionary response, we compared the newly established North and South American wing size clines of Drosophila subobscura. The new clines are based on latitudinal variation in cell area in North America and cell number in South America. The ancestral European cline is also based on latitudinal variation in cell number. The difference in the cellular basis of wing size variation in the American clines, which are roughly the same age, together with the similar cellular basis of the new South American cline and the ancient European one, suggest that the antiquity of a cline does not explain its cellular basis. Furthermore, the results indicate that wing size as a whole, rather than its cellular basis, is under selection. The different cellular bases of different size clines are most likely explained either entirely by chance or by different patterns of genetic variance,or its expression,in founding populations. [source]


    EMPIRICAL EVIDENCE FOR AN OPTIMAL BODY SIZE IN SNAKES

    EVOLUTION, Issue 2 2003
    Scott M. Boback
    Abstract The concept of optimal size has been invoked to explain patterns in body size of terrestrial mammals. However, the generality of this phenomenon has not been tested with similarly complete data from other taxonomic groups. In this study we describe three statistical patterns of body size in snakes, all of which indicate an optimal length of 1.0 m. First, a distribution of largest body lengths of 618 snake species had a single mode at 1.0 m. Second, we found a positive relationship between the size of the largest member of an island snake assemblage and island area and a negative relationship between the size of the smallest member of an island snake assemblage and island area. Best-fit lines through these data cross at a point corresponding to 1.0 m in body length, the presumed optimal size for a one-species island. Third, mainland snake species smaller than 1.0 m become larger on islands whereas those larger than 1.0 m become smaller on islands. The observation that all three analyses converge on a common body size is concordant with patterns observed in mammals and partial analyses of four other disparate animal clades. Because snakes differ so strikingly from mammals (ectotherms, gape-limited predators, elongate body shape) the concordant patterns of these two groups provide strong evidence for the evolution of an optimal body size within independent monophyletic groups. However, snakes differ from other taxonomic groups that have been studied in exhibiting a body size distribution that is not obviously skewed in either direction. We suggest that idiosyncratic features of the natural history of ectotherms allow relatively unconstrained distributions of body size whereas physiological limitations of endotherms constrain distributions of body size to a right skew. [source]


    A STATISTICAL TEST OF UNBIASED EVOLUTION OF BODY SIZE IN BIRDS

    EVOLUTION, Issue 12 2002
    Folmer Bokma
    Abstract., Of the approximately 9500 bird species, the vast majority is small-bodied. That is a general feature of evolutionary lineages, also observed for instance in mammals and plants. The avian interspecific body size distribution is right-skewed even on a logarithmic scale. That has previously been interpreted as evidence that body size evolution has been biased. However, a procedure to test for unbiased evolution from the shape of body size distributions was lacking. In the present paper unbiased body size evolution is defined precisely, and a statistical test is developed based on Monte Carlo simulation of unbiased evolution. Application of the test to birds suggests that it is highly unlikely that avian body size evolution has been unbiased as defined. Several possible explanations for this result are discussed. A plausible explanation is that the general model of unbiased evolution assumes that population size and generation time do not affect the evolutionary variability of body size; that is, that micro- and macroevolution are decoupled, which theory suggests is not likely to be the case. [source]


    MEASURING PROBABILISTIC REACTION NORMS FOR AGE AND SIZE AT MATURATION

    EVOLUTION, Issue 4 2002
    Mikko Heino
    Abstract We present a new probabilistic concept of reaction norms for age and size at maturation that is applicable when observations are carried out at discrete time intervals. This approach can also be used to estimate reaction norms for age and size at metamorphosis or at other ontogenetic transitions. Such estimations are critical for understanding phenotypic plasticity and life-history changes in variable environments, assessing genetic changes in the presence of phenotypic plasticity, and calibrating size- and age-structured population models. We show that previous approaches to this problem, based on regressing size against age at maturation, give results that are systematically biased when compared to the probabilistic reaction norms. The bias can be substantial and is likely to lead to qualitatively incorrect conclusions; it is caused by failing to account for the probabilistic nature of the maturation process. We explain why, instead, robust estimations of maturation reaction norms should be based on logistic regression or on other statistical models that treat the probability of maturing as a dependent variable. We demonstrate the utility of our approach with two examples. First, the analysis of data generated for a known reaction norm highlights some crucial limitations of previous approaches. Second, application to the northeast arctic cod (Gadus morhua) illustrates how our approach can be used to shed new light on existing real-world data. [source]


    NUPTIAL GIFTS AND THE EVOLUTION OF MALE BODY SIZE

    EVOLUTION, Issue 3 2002
    Kenneth M. Fedorka
    Abstract In many insect systems, males donate nuptial gifts to insure an effective copulation or as a form of paternal investment. However, if gift magnitude is both body size-limited and positively related to fitness, then the opportunity exists for the gift to promote the evolution of large male size. In the striped ground cricket, Allonemobius socius, males transfer a body size-limited, somatic nuptial gift that is comprised primarily of hemolymph. To address the implications of this gift on male size evolution, we quantified the intensity and direction of natural (fecundity) and sexual (mating success) selection over multiple generations. We found that male size was under strong positive sexual selection throughout the breeding season. This pattern of selection was similar in successive generations spanning multiple years. Male size was also under strong natural selection, with the largest males siring the most offspring. However, multivariate selection gradients indicated that gift size, and not male size, was the best predictor of female fecundity. In other words, direct fecundity selection for larger gifts placed indirect positive selection on male body size, supporting the hypothesis that nuptial gifts can influence the evolution of male body size in this system. Although female size was also under strong selection due to a size related fecundity advantage, it did not exceed selection on male size. The implications of these results with regard to the maintenance of the female-biased size dimorphic system are discussed. [source]


    COMPETITION FOR MARKET SHARE OR FOR MARKET SIZE: OLIGOPOLISTIC EQUILIBRIA WITH VARYING COMPETITIVE TOUGHNESS,

    INTERNATIONAL ECONOMIC REVIEW, Issue 3 2007
    Claude D'Aspremont
    For an industry producing a composite commodity, we propose a comprehensive concept of oligopolistic equilibrium, allowing for a parameterized continuum of regimes varying in competitive toughness. Each firm sets simultaneously its price and its quantity under two constraints, relative to its market share and to market size. The price and the quantity equilibrium outcomes always belong to the set of oligopolistic equilibria. When firms are identical and we let their number increase, any sequence of symmetric oligopolistic equilibria converges to the monopolistic competition outcome. Further results are derived in the symmetric CES case, concerning in particular the collusive solution enforceability. [source]


    PRODUCT MARKET AND THE SIZE,WAGE DIFFERENTIAL*

    INTERNATIONAL ECONOMIC REVIEW, Issue 1 2002
    SHOUYONG SHI
    Using directed search to model the product market and the labor market, I show that large plants can pay higher wages to homogeneous workers and earn higher expected profit per worker than small plants, although plants are identical except size. A large plant charges a higher price for its product and compensates buyers with a higher service probability. To capture this size- related benefit, large plants try to become larger by recruiting at high wages. This size,wage differential survives labor market competition because a high wage is harder to get than a low wage. Moreover, the size,wage differential increases with the product demand when demand is initially low and falls when demand is already high. [source]


    An analytical model for the performance evaluation of stack-based Web cache replacement algorithms

    INTERNATIONAL JOURNAL OF COMMUNICATION SYSTEMS, Issue 1 2010
    S. Messaoud
    Abstract Web caching has been the solution of choice to web latency problems. The efficiency of a Web cache is strongly affected by the replacement algorithm used to decide which objects to evict once the cache is saturated. Numerous web cache replacement algorithms have appeared in the literature. Despite their diversity, a large number of them belong to a class known as stack-based algorithms. These algorithms are evaluated mainly via trace-driven simulation. The very few analytical models reported in the literature were targeted at one particular replacement algorithm, namely least recently used (LRU) or least frequently used (LFU). Further they provide a formula for the evaluation of the Hit Ratio only. The main contribution of this paper is an analytical model for the performance evaluation of any stack-based web cache replacement algorithm. The model provides formulae for the prediction of the object Hit Ratio, the byte Hit Ratio, and the delay saving ratio. The model is validated against extensive discrete event trace-driven simulations of the three popular stack-based algorithms, LRU, LFU, and SIZE, using NLANR and DEC traces. Results show that the analytical model achieves very good accuracy. The mean error deviation between analytical and simulation results is at most 6% for LRU, 6% for the LFU, and 10% for the SIZE stack-based algorithms. Copyright © 2009 John Wiley & Sons, Ltd. [source]


    INFLUENCE OF SAMPLE SIZE AND SHAPE ON TRANSPORT PARAMETERS DURING DRYING OF SHRINKING BODIES

    JOURNAL OF FOOD PROCESS ENGINEERING, Issue 2 2007
    NAJMUR RAHMAN
    ABSTRACT An experimental investigation on the influence of sample size and shape on heat and mass transport parameters under natural convection air-drying is presented. Potato cylinders with length of 0.05 m and thicknesses of 0.005, 0.008, 0.010 and 0.016 m, and circular slices with diameter of 0.05 m and thickness of 0.01 m were dried in a laboratory scale hot-air cabinet dryer. Results indicate that each transport parameter exhibits a linear relationship with sample thickness. Convective heat and mass transfer coefficients (hcand hm) decreased whereas moisture diffusion coefficient (Deff) increased with increasing thickness. Considering no sample shrinkage effect in the parameter analysis, for the thickness range considered, the values of hcare found to be underestimated in the range of 29.0,30.6%, whereas those of hmand Deff are overestimated in the range of 33.7,38.0% and 75.9,128.1%, respectively. Using Levenberg,Marquardt algorithm for optimization, a correlation for Biot number for mass transfer (Bim) as a function of drying time and sample thickness is proposed. A close agreement was observed between dimensionless moisture contents predicted by this relation and those obtained from experiments for different sample thicknesses at drying air temperature of 60C. For the same thickness and drying conditions, circular slices caused an increase in each transport parameter significantly. [source]


    ATTRITION EVALUATION FOR SELECTED AGGLOMERATED FOOD POWDERS: THE EFFECT OF AGGLOMERATE SIZE AND WATER ACTIVITY

    JOURNAL OF FOOD PROCESS ENGINEERING, Issue 1 2001
    HONG YAN
    ABSTRACT Investigation of the attrition of agglomerates is very important for assessing the agglomerate strength, compaction characteristics, and quality control. A one-term exponential attrition index model and the Hausner ratio were used to study the effects of agglomerate size and water activity on the attrition kinetics of some selected agglomerated food powders. It was found that the agglomerate size and water activity played significant roles in affecting the attrition: the larger the agglomerate size and the higher the water activity, the higher the attrition index under the same tap number. The Hausner ratio was well correlated with the attrition index at high tap numbers and might be used as a simple index to evaluate attrition severity for agglomerates. Knowing the effects of agglomerate size and water activity is very useful to minimize the attrition phenomenon during the handling and processing of agglomerated powders. [source]


    RHEOLOGICAL PROPERTIES OF NONCOHESIVE APPLE DISPERSION WITH HELICAL AND VANE IMPELLERS: EFFECT OF CONCENTRATION AND PARTICLE SIZE

    JOURNAL OF FOOD PROCESS ENGINEERING, Issue 5 2000
    DENIS CANTÚ-LOZANO
    ABSTRACT The proportionality constant, ks, between shear rate, ,, and agitation velocity, N, for a helical ribbon-screw (HRS) agitator was 17.8. Using the HRS agitator, values of consistency index K and the flow behavior index n of 14 apple pulp suspensions at seven different solids concentrations and two average particle diameters 0.71 mm and 1.21 mm were determined; in addition, values of the Casson viscosity ,c and yield stress ,OC were also calculated. The magnitudes of K increased and of n decreased with increase in pulp concentration. Experimental values of the vane yield stress, ,O,, measured with a six-blade vane increased with increase in pulp content. The values of ,OC obtained using the Casson model were close to the experimental values ,O,. The effect of particle size on the relative viscosity, ,r, was correlated with Peclet number. [source]


    EFFECT OF BREADING PARTICLE SIZE ON COATING ADHESION IN BREADED, FRIED CHICKEN BREASTS

    JOURNAL OF FOOD QUALITY, Issue 2 2004
    MOHAMAD YUSOF MASKAT
    ABSTRACT The effect of particle size on coating adhesion was measured for battered chicken breasts. Bread crumbs were separated into small (, 250 ,m), medium (250 ,m-850 ,m), and large (> 850 ,m) particles. Chicken breasts were battered, breaded, and deep-fat fried for 240 s at 160C. Fried products were analyzed for coating adhesion, moisture content, and yield parameters. Coating adhesion was highest in coatings formed from small particle size breading, and lowest in those made from large particle size breading. Chicken breasts coated using small particle size breading had higher moisture in the surface region of the meat as well as in the coating. SEM of the coatings showed greater merging between the breading and the batter with decreasing breading particle size. No significant differences were observed in coating pickup, cooking loss, or yield between samples coated with different particle size breading. [source]


    EFFECTS OF BITE SIZE ON THE SENSORY PROPERTIES OF VANILLA CUSTARD DESSERTS

    JOURNAL OF SENSORY STUDIES, Issue 3 2007
    JON F. PRINZ
    ABSTRACT A trained panel of 19 subjects were asked to rate a number of sensory attributes of commercially available vanilla custard desserts. Stimuli were placed in plastic cups and were sampled using 11-mm-diameter straws. In total, 304 samples were weighed before and after sampling and the volume ingested was calculated. The subjects were categorized into two groups on the basis of the mean volume ingested per sample (< and >10.6 mL). There were significant differences in the ratings between the two groups for temperature, creamy, astringent, melting and airy mouthfeels and rough and fatty after-feel. We suggest that in sensory testing, it is important to either control or measure bite size to reduce intersubject variability. Manufacturers and caterers may also be able to modify the perception of their products by providing cues to the appropriate bite size by controlling the size of the spoon or container provided. [source]


    MEASUREMENT OF FIRMNESS OF FRESH-CUT SLICED TOMATO USING PUNCTURE TESTS , STUDIES ON SAMPLE SIZE, PROBE SIZE AND DIRECTION OF PUNCTURE

    JOURNAL OF TEXTURE STUDIES, Issue 5 2007
    MILZA M. LANA
    ABSTRACT In order to investigate the firmness of tomato slices, two experiments were performed. In the first one, Monte Carlo simulation was used to study the variation in firmness within and between slices. Adding more slices and more measurements per slice reduced the SD, but in general, the efficiency of adding more slices was higher. In the second experiment, the firmness of tomato slices was measured by puncture test during storage, using one of three flat-tipped cylindrical probes (3.5-, 2.5- and 1.5-mm diameter) in two directions, along or perpendicular to the main axis of the fruit. Changes in firmness were studied by nonlinear regression analysis. The same model could be applied to all combinations of probe size and direction with the same correction for shear and compression. It suggests that shear and compression forces decay with storage time according to the same mechanism, irrespective of the measurement direction. PRACTICAL APPLICATIONS Methodologies for both firmness evaluation and data analysis were presented. Monte Carlo simulation was used to optimize the number of samples for firmness assays. After calculating the experimental SD from preliminary experimental results, simulations were performed with different numbers of replicates and measurements per replicate, to find an optimal experimental design where the SD is minimized. Using nonlinear regression, the effects on firmness of probe size, puncture direction in relation to the plant tissue and storage time can be analyzed simultaneously. The incorporation of a correction factor to account for differences in firmness due to probe size was proposed. The relative influence of shear (s) and compression force (c) on the observed force is estimated. Results of interest for the industry were presented, confirming previous findings that the firmness of ripened tomato slices measured by puncture analysis does not change significantly during short-term storage at low temperature. [source]