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population
population

... • The frequency of an allele in a population can be calculated – For diploid organisms, the total number of alleles at a locus is the total number of individuals x 2 – The total number of dominant alleles at a locus is 2 alleles for each homozygous dominant individual plus 1 allele for each heteroz ...
Sex chromosomes and sex determination
Sex chromosomes and sex determination

... Sex-determining systems in insects exhibit a wide range of diversity. In addition to XX/XY and ZW/ZZ sex-determining systems, some taxa have evolved systems that have not been found in any other classes: for example, the haploid/diploid sexdetermining system or, more exactly, the complementary sex-d ...
Reconstruction of a 450-My-old ancestral vertebrate protokaryotype
Reconstruction of a 450-My-old ancestral vertebrate protokaryotype

... different chromosomes in the ancestral eutherian protokaryotype. Yang et al. [4], using chromosome paints, proposed that these associations represent the eutherian chromosomes EUT 7 and 21. The respective genes of the first and larger association of segments from HSA 12p/q and 22q map on the duplica ...
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as Microsoft Word - Edinburgh Research Explorer

... minimum of two of the above criteria, although clearly larger numbers of animals need to be studied to confirm these findings. ...
Identification and mapping of RAPD and RFLP markers linked to a
Identification and mapping of RAPD and RFLP markers linked to a

... locus. Then the maps by Barzen et al. (1995) and Schondelmaier et al. (1995), including RFLP, RAPD and morphological markers, were used to produce a joint map of the region in which the restorer locus was situated. Within the progeny used for BSA, a 1 : 1 ratio fitted the observed ratio of: (1) the ...
Text S1 Snitkin and Segrè, Epistatic interaction maps relative to
Text S1 Snitkin and Segrè, Epistatic interaction maps relative to

... tend to reside in the same pathways [7, 8]. Therefore we expected that a more accurate quantification of epistasis would result in a stronger relationship between genetic congruence and common pathway membership. A comparison of the performance of different metrics averaged across all phenotypes sho ...
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Recombination and the Frequency Spectrum in

... There is no gene conversion and the rate of crossing over is constant per base pair. Tracing the ancestral lineages of the sample backward in time, there are two possible genealogical events. Lineages can coalesce in the usual way, or they can split into two as a result of a crossing-over event. The ...
AP Biology Chapter 14 Study Guide
AP Biology Chapter 14 Study Guide

... 10. What were the actual colors of the F1 generation plants? 11. What were the actual colors of the F2 generation plants? 12. What were the ratios of purple to white flowers in the F2 generation? 13. What explanation did Mendel give for these results? 14. Did these ratios hold true for traits other ...
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comparative evolution and development of the butterfly eyespot and

... focused on the eyespots of the tropical African butterfly Bicyclus anynana (discussed in Brakefield 1998). In this system, it has been shown that there is additive genetic variance for different characteristics of the eyespot such as size, color proportion, and shape (Monteiro et al. 1994, 1997a, 19 ...
recessive lozenge-shaped-fly-eye "alleles" in trans: recessive
recessive lozenge-shaped-fly-eye "alleles" in trans: recessive

... phage happen to have a MUCH greater rate of recombination per unit DNA than fruit flies or garden peas In rII, smallest non-0 recombination rate measured was 0.02 cM (mutants 1 bp apart) (2 NP/10,000 total) In my first effort at fine-structure mapping in flies, I measured 0.007 cM (one recombinant) ...
Animal Behaviour SPECIAL ISSUE: KIN SELECTION
Animal Behaviour SPECIAL ISSUE: KIN SELECTION

... phenomenon may indicate that behavioural outcomes are constrained by a mechanistic framework with finite capacity for variation. Thus, in contrast to the concept of the phenotypic gambit, there may be limitations to behavioural optimization, much like the constraints imposed by competing ecological s ...
Mutualism and asexual reproduction influence recognition genes in
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... offspring even though it is more costly than asexual reproduction (e.g., Barton & Charlesworth 1998; Otto 2003). This costly reproductive strategy could be maintained because recombination acts to provide advantageous genotypes necessary for adaptation to changing environments or because recombinati ...
The Evolution of Sex Determination in Animals
The Evolution of Sex Determination in Animals

... Although it is possible that some sex-determining systems are selectively neutral, the phylogenetic pattern of GSD and ESD suggest a selective explanation for their diversity. Because sex determination has a direct impact on the sex ratio, sex ratio selection is expected to strongly influence evolut ...
ADAPT, MOVE OR PERISH THE INTERACTION OF GENETICS
ADAPT, MOVE OR PERISH THE INTERACTION OF GENETICS

... Habitat loss and degradation, and human-induced climate change are two of the main current threats to biodiversity. While the impacts of these pressures separately on species survival are being investigated extensively, we have only just begun to unravel the combined impact of these two pressures on ...
empirical evidence for bet hedging Modes of response to
empirical evidence for bet hedging Modes of response to

... traits maximize geometric-mean fitness of their carriers across generations but do not maximize the expected fitness within a generation [37], bet-hedging adaptations appear to be detrimental if observed over short periods of time—even under ‘normal’ or average conditions. Bet-hedging traits are eit ...
phenotypic correlations - Watson et al (v91)
phenotypic correlations - Watson et al (v91)

... Pomp & Lightfoot 2009, Chevillon et al 1997, Lenski 1988a/b, Kim Huh & Fay 2009). This means that phenotypic correlations can change as a result of evolution by natural selection (Delph et al 2011). Examples have been documented with respect to fore and hindlimb correlations in mammals (Young et al. ...
Advantages and Disadvantages of Asexual Reproduction
Advantages and Disadvantages of Asexual Reproduction

... game to show the difference between inheritance of traits in asexual and sexual organisms. Since these students have not yet learned about genotypes and phenotypes, it is not necessary to introduce those terms unless you wish to. Also, there is no ‘dominant’ or ‘recessive’ gene in this scenario, pri ...
Gene Flow Gene Flow Between Two Demes
Gene Flow Gene Flow Between Two Demes

... sequence level, there is often so much variation that the probability of two randomly chosen genes being identical, even within the same deme, is very small and therefore hard to estimate reliably. “Heterozygosity” within demes often approaches one even when the demes’ gene pools are very different, ...
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Book Reviews 103 Wertheimer`s analysis clearly

... Perhaps the most significant problem in this book involves defining what evidence would be required to settle the issue of whether female orgasm is an adaptation or a byproduct. In Chapter 1, Lloyd cites West-Eberhard’s (1992) definition of an adaptation: a character for which “there is some evidenc ...
Technical standards and guidelines for reproductive screening in
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... The Ashkenazi Jewish population represents a distinct subpopulation characterized by a specific religion (Judaism), a defined place of origin (Middle East) and a well-defined pattern of migration (eastern Europe, United States). Traditionally, Jews have been divided into three major groups according ...
Formation of vestigial organs
Formation of vestigial organs

... than be directed, as long as those changes do not affect the organism’s fitness. It is possible that the reduction of vestigial structures could be the result of this build-up of random genetic mutation because all that is needed for it to occur is something that all vestigial structures have in com ...
Lecture PDF - Carol Eunmi LEE
Lecture PDF - Carol Eunmi LEE

... Calculating Allele Frequencies from # of Individuals • The frequency of an allele in a population can be calculated from # of individuals: – For diploid organisms, the total number of alleles at a locus is the total number of individuals x 2 – The total number of dominant alleles at a locus is 2 ...
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9 Selection on Correlated Characters

... Was selection targeted specifically at beak depth, or was general size the primary determinant of survival? How can we determine the actual target of selection? In addition, those traits are all genetically correlated, so selection on one trait can result in a change in the other. Here we will see h ...
Lecture PPT - Carol Eunmi LEE
Lecture PPT - Carol Eunmi LEE

... Testing for Deviaton from HardyWeinberg Expectations • A c2 goodness-of-fit test can be used to determine if a population is significantly different from the expections of Hardy-Weinberg equilibrium. • If we have a series of genotype counts from a population, then we can compare these counts to the ...
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Koinophilia



Koinophilia is an evolutionary hypothesis concerning sexual selection which proposes that animals seeking mate preferentially choose individuals with a minimum of unusual features. Koinophilia intends to explain the clustering of organisms into species and other issues described by Darwin's Dilemma. The term derives from the Greek, koinos, ""the usual"", and philos, ""fondness"".Natural selection causes beneficial inherited features to become more common and eventually replace their disadvantageous counterparts. A sexually-reproducing animal would be expected to avoid individuals with unusual features, and to prefer to mate with individuals displaying a predominance of common or average features. This means that mates displaying mutant features are also avoided. This is advantageous because most mutations that manifest themselves as changes in appearance, functionality or behavior, are disadvantageous. Because it is impossible to judge whether a new mutation is beneficial or not, koinophilic animals avoid them all, at the cost of avoiding the occasional beneficial mutation. Thus, koinophilia, although not infallible in its ability to distinguish fit from unfit mates, is a good strategy when choosing a mate. A koinophilic choice ensures that offspring are likely to inherit features that have been successful in the past.Koinophilia differs from assortative mating, where ""like prefers like"". If like preferred like, leucistic animals (such as white peacocks) would be sexually attracted to one another, and a leucistic subspecies would come into being. Koinophilia predicts that this is unlikely because leucistic animals are attracted to the average in the same way as other animals. Since non-leucistic animals are not attracted by leucism, few leucistic individuals find mates, and leucistic lineages will rarely form.Koinophilia provides simple explanations for the rarity of speciation (in particular Darwin's Dilemma), evolutionary stasis, punctuated equilibria, and the evolution of cooperation. Koinophilia might also contribute to the maintenance of sexual reproduction, preventing its reversion to the much simpler and inherently more advantageous asexual form of reproduction.The koinophilia hypothesis is supported by research into the physical attractiveness of human faces by Judith Langlois and her co-workers. They found that the average of two human faces was more attractive than either of the faces from which that average was derived. The more faces (of the same gender and age) that were used in the averaging process the more attractive and appealing the average face became. This work into averageness supports koinophilia as an explanation of what constitutes a beautiful face, and how the individuality of a face is recognized.
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