Information about Theory Of Evolution
This article is about evolution in biology. For other uses, see Evolution (disambiguation).
“Theory of evolution” redirects here. For more on how evolution is defined, see Evolution as theory and fact.
For a less technical and generally accessible introduction to the topic, see .
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| Evolution |
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Adaptation Genetic drift Gene flow Mutation Natural selection Speciation |
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Evidence History Modern synthesis Social effect / Objections |
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Ecological genetics Evolutionary development Human evolution Molecular evolution Evolutionary history of life Phylogenetics Population genetics |
In biology, evolution is the change in the inherited traits of a population from generation to generation. These traits are the expression of genes that are copied and passed on to offspring during reproduction. Mutations in these genes can produce new or altered traits, resulting in heritable differences (genetic variation) between organisms. New traits can also come from transfer of genes between populations, as in migration, or between species, in horizontal gene transfer. Evolution occurs when these heritable differences become more common or rare in a population, either non-randomly through natural selection or randomly through genetic drift.
Natural selection is a process that causes heritable traits that are helpful for survival and reproduction to become more common, and harmful traits to become more rare. This occurs because organisms with advantageous traits pass on more copies of these heritable traits to the next generation.[][1] Over many generations, adaptations occur through a combination of successive, small, random changes in traits, and natural selection of those variants best-suited for their environment.[2] In contrast, genetic drift produces random changes in the frequency of traits in a population. Genetic drift arises from the role chance plays in whether a given individual will survive and reproduce.
One definition of a species is a group of organisms that can reproduce with one another and produce fertile offspring. However, when a species is separated into populations that are prevented from interbreeding, mutations, genetic drift, and the selection of novel traits cause the accumulation of differences over generations and the emergence of new species.[3] The similarities between organisms suggest that all known species are descended from a common ancestor (or ancestral gene pool) through this process of gradual divergence.[0]
The theory of evolution by natural selection was proposed roughly simultaneously by both Charles Darwin and Alfred Russel Wallace, and set out in detail in Darwin's 1859 book On the Origin of Species.[5] It encountered initial resistance from religious authorities who believed humans were divinely set apart from the animal kingdom. In the 1930s, Darwinian natural selection was combined with Mendelian inheritance to form the modern evolutionary synthesis,[5] in which the connection between the units of evolution (genes) and the mechanism of evolution (natural selection) was made. This powerful explanatory and predictive theory has become the central organizing principle of modern biology, providing a unifying explanation for the diversity of life on Earth.[6]
Heredity

DNA structure. Bases are in the center, surrounded by phosphate–sugar chains in a double helix
- For more details on this topic, see , , and .
The complete set of observable traits that make up the structure and behavior of an organism is called its phenotype. These traits come from the interaction of its genotype with the environment.[9] As a result, not every aspect of an organism's phenotype is inherited. Suntanned skin results from the interaction between a person's genotype and sunlight; thus, a suntan is not hereditary. However, people have different responses to sunlight, arising from differences in their genotype; a striking example is individuals with the inherited trait of albinism, who do not tan and are highly sensitive to sunburn.[10]
Genes are regions within DNA molecules that contain genetic information.[8] DNA is a long molecule with four types of bases attached along its length. Different genes have different sequences of bases; it is the sequence of these bases that encodes genetic information. Within cells, the long strands of DNA associate with proteins to form structures called chromosomes. A specific location within a chromosome is known as a locus. If the DNA sequence at a locus varies between individuals, the different forms of this sequence are called alleles. DNA sequences can change through mutations, producing new alleles. If a mutation occurs within a gene, the new allele may affect the trait that the gene controls, altering the phenotype of the organism. However, while this simple correspondence between an allele and a trait works in some cases, most traits are more complex and are controlled by multiple interacting genes.[11][12]
Variation
- For more details on this topic, see and .
Because an individual's phenotype results from the interaction of their genotype with the environment, the variation in phenotypes in a population reflects the variation in these organisms' genotypes.[12] The modern evolutionary synthesis defines evolution as the change over time in this genetic variation.[13] The frequency of one particular allele will fluctuate, becoming more or less prevalent relative to other forms of that gene. Evolutionary forces act by driving these changes in allele frequency in one direction or another. Variation disappears when an allele reaches the point of fixation — when it either disappears from the population or replaces the ancestral allele entirely.[14]
Variation comes from mutations in genetic material, migration between populations (gene flow), and the reshuffling of genes through sexual reproduction. Variation also comes from exchanges of genes between different species; for example, through horizontal gene transfer in bacteria, and hybridization in plants.[15] Despite the constant introduction of variation through these processes, most of the genome of a species is identical in all individuals of that species.[16] However, even relatively small changes in genotype can lead to dramatic changes in phenotype: chimpanzees and humans differ in only about 5% of their genomes.[17]
Mutation
- For more details on this topic, see and .
Duplication of part of a chromosome
Changes in chromosome number may also involve the breakage and rearrangement of DNA within chromosomes. For example, two chromosomes in the Homo genus fused to produce human chromosome 2; this fusion did not occur in the chimpanzee lineage and chimpanzees retain these separate chromosomes.[29] In evolution, the most important role of such chromosomal rearrangements may be to accelerate the divergence of a population into new species by preserving genetic differences within populations.[30]
Sequences of DNA that can move about the genome, such as transposons, make up a major fraction of the genetic material of plants and animals, and may have been important in the evolution of genomes.[31] For example, more than a million copies of the Alu sequence are present in the human genome, and these sequences have now been recruited to perform functions such as regulating gene expression.[32] Another effect of these mobile DNA sequences is that when they move within a genome, they can mutate or delete existing genes and thereby produce genetic diversity.[33]
Recombination
- For more details on this topic, see and .
In asexual organisms, genes are inherited together, or linked, as they cannot mix with genes in other organisms during reproduction. However, the offspring of sexual organisms contain a random mixture of their parents' chromosomes that is produced through independent assortment. In the related process of genetic recombination, sexual organisms can also exchange DNA between two matching chromosomes.[34] These shuffling processes can allow even alleles that are close together in a strand of DNA to be inherited independently. However, as only about one recombination event occurs per million base pairs in humans, genes close together on a chromosome may not be shuffled away from each other, and tend to be inherited together.[35] This tendency is measured by finding how often two alleles occur together, which is called their linkage disequilibrium. A set of alleles that is usually inherited in a group is called a haplotype, and this co-inheritance can indicate that the locus is under positive selection (see below).[36]
Recombination in sexual organisms helps to remove harmful mutations and retain beneficial mutations.[37] Consequently, when alleles cannot be separated by recombination – such as in mammalian Y chromosomes, which pass intact from fathers to sons – harmful mutations accumulate.[38][39] In addition, recombination can produce individuals with new and advantageous gene combinations. These positive effects of recombination are balanced by the fact that this process can cause mutations and separate beneficial combinations of genes.[37] The optimal rate of recombination for a species is therefore a trade-off between conflicting factors.
Mechanisms
There are three basic mechanisms of evolutionary change: natural selection, genetic drift, and gene flow. Natural selection favors genes that improve capacity for survival and reproduction. Genetic drift is the random sampling of a generation's genes during reproduction, causing random changes in the frequency of alleles, and gene flow is the transfer of genes within and between populations. The relative importance of natural selection and genetic drift in a population varies depending on the strength of the selection and the effective population size, which is the number of individuals capable of breeding.[40] Natural selection usually predominates in large populations, while genetic drift dominates in small populations. The dominance of genetic drift in small populations can even lead to the fixation of slightly deleterious mutations.[41] As a result, changing population size can dramatically influence the course of evolution. Population bottlenecks, where the population shrinks temporarily and therefore loses genetic variation, result in a more uniform population.[14] Bottlenecks also result from alterations in gene flow such as decreased migration, expansions into new habitats, or population subdivision.[40]Natural selection

Natural selection of a population for dark coloration.
- For more details on this topic, see and .
Natural selection is the process by which genetic mutations that enhance reproduction become, and remain, more common in successive generations of a population. It has often been called a "self-evident" mechanism because it necessarily follows from three simple facts:
- * Heritable variation exists within populations of organisms.
- * Organisms produce more offspring than can survive.
- * These offspring vary in their ability to survive and reproduce.
These conditions produce competition between organisms for survival and reproduction. Consequently, organisms with traits that give them an advantage over their competitors pass these advantageous traits on, while traits that do not confer an advantage are not passed on to the next generation.
The central concept of natural selection is the evolutionary fitness of an organism. This measures the organism's genetic contribution to the next generation. However, this is not the same as the total number of offspring: instead fitness measures the proportion of subsequent generations that carry an organism's genes.[42] Consequently, if an allele increases fitness more than the other alleles of that gene, then with each generation this allele will become more common within the population. These traits are said to be "selected for". Examples of traits that can increase fitness are enhanced survival, and increased fecundity. Conversely, the lower fitness caused by having a less beneficial or deleterious allele results in this allele becoming rarer — they are "selected against".[1] Importantly, the fitness of an allele is not a fixed characteristic, if the environment changes, previously neutral or harmful traits may become beneficial and previously beneficial traits become harmful.[0]
Natural selection within a population for a trait that can vary across a range of values, such as height, can be categorized into three different types. The first is directional selection, which is a shift in the average value of a trait over time — for example organisms slowly getting taller.[43] Secondly, disruptive selection is selection for extreme trait values and often results in two different values becoming most common, with selection against the average value. This would be when either short or tall organisms had an advantage, but not those of medium height. Finally, in stabilizing selection there is selection against extreme trait values on both ends, which causes a decrease in variance around the average value.[44] This would, for example, cause organisms to slowly become all the same height.
A special case of natural selection is sexual selection, which is selection for any trait that increases mating success by increasing the attractiveness of an organism to potential mates.[45] Traits that evolved through sexual selection are particularly prominent in males of some animal species, despite traits such as cumbersome antlers, mating calls or bright colors that attract predators, decreasing the survival of individual males.[46] This survival disadvantage is balanced by higher reproductive success in males that show these hard to fake, sexually selected traits.[47]
An active area of research is the unit of selection, with natural selection being proposed to work at the level of genes, cells, individual organisms, groups of organisms and even species.[48][49] None of these models are mutually-exclusive and selection may act on multiple levels simultaneously.[50] Below the level of the individual, genes called transposons try to copy themselves throughout the genome.[51] Selection at a level above the individual, such as group selection, may allow the evolution of co-operation, as discussed below.[52]
Simulation of genetic drift of 20 unlinked alleles in populations of 10 (top) and 100 (bottom). Drift is more rapid in the smaller population.
Genetic drift
- For more details on this topic, see and .
Genetic drift is the change in allele frequency from one generation to the next that occurs because alleles in the offspring generation are a random sample of those in the parent generation, and are thus subject to sampling error.[14] As a result, when selective forces are absent or relatively weak, allele frequencies tend to "drift" upward or downward in a random walk. This drift halts when an allele eventually becomes fixed, either by disappearing from the population, or replacing the other alleles entirely. Genetic drift may therefore eliminate some alleles from a population due to chance alone, and two separate populations that began with the same genetic structure can drift apart by random fluctuation into two divergent populations with different sets of alleles.[53] The time for an allele to become fixed by genetic drift depends on population size, with fixation occurring more rapidly in smaller populations.[54]
Although natural selection is responsible for adaptation, the relative importance of the two forces of natural selection and genetic drift in driving evolutionary change in general is an area of current research in evolutionary biology.[55] These investigations were prompted by the neutral theory of molecular evolution, which proposed that most evolutionary changes are the result the fixation of neutral mutations that do not have any immediate effects on the fitness of an organism.[56] Hence, in this model, most genetic changes in a population are the result of constant mutation pressure and genetic drift.[57]
Gene flow
- For more details on this topic, see , , and .
Gene flow is the exchange of genes between populations, which are usually of the same species.[58] Examples of gene flow within a species include the migration and then breeding of organisms, or the exchange of pollen. Gene transfer between species includes the formation of hybrid organisms and horizontal gene transfer.
Migration into or out of a population can change allele frequencies. Immigration may add new genetic material to the established gene pool of a population. Conversely, emigration may remove genetic material. As barriers to reproduction between two diverging populations are required for the populations to become new species, gene flow may slow this process by spreading genetic differences between the populations. Gene flow is hindered by mountain ranges, oceans and deserts or even man-made structures such as the Great Wall of China, which has hindered the flow of plant genes.[59]
Depending on how far two species have diverged since their last common ancestor, it may still be possible for them to produce offspring, as with horses and donkeys mating to produce mules.[60] Such hybrids are generally infertile, due to the two different sets of chromosomes being unable to pair up during meiosis. In this case, closely-related species may regularly interbreed, but hybrids will be selected against and the species will remain distinct. However, viable hybrids are occasionally formed and these new species can either have properties intermediate between their parent species, or possess a totally new phenotype.[61] The importance of hybridization in creating new species of animals is unclear, although cases have been seen in many types of animals,[62] with the gray tree frog particularly well-studied.[63]
Hybridization is, however, an important means of speciation in plants, since polyploidy (having more than two copies of each chromosome) is tolerated in plants more readily than in animals.[64] Polyploidy is important in hybrids as it allows reproduction, with the two different sets of chromosomes each being able to pair with an identical partner during meiosis.[65] Polyploids also have more genetic diversity, which allows them to avoid inbreeding depression in small populations.[66]
Horizontal gene transfer is the transfer of genetic material from one organism to another organism that is not its offspring, this is most common among bacteria.[67] In medicine, this contributes to the spread of antibiotic resistance, as when one bacteria acquires resistance genes it can rapidly transfer them to other species.[68] Horizontal transfer of genes from bacteria to eukaryotes such as the yeast Saccharomyces cerevisiae and the adzuki bean beetle Callosobruchus chinensis may also have occurred.[69][70] Viruses can also carry DNA between organisms, allowing transfer of genes even across biological domains.[71] Gene transfer has also occurred within eukaryotic cells, from the chloroplast and mitochondrial genomes to nuclear genomes.[72]
Outcomes
Evolution influences every aspect of the form and behavior of organisms. Most prominent are the specific behavioral and physical adaptations that are the outcome of natural selection. These adaptations increase fitness by aiding activities such as finding food, avoiding predators or attracting mates. Organisms can also respond to selection by co-operating with each other, usually by aiding their relatives or engaging in mutually-beneficial partnerships. In the longer term, evolution produces new species through splitting ancestral populations of organisms into new groups that are unable to breed with one another.These outcomes of evolution are sometimes divided into macroevolution, which is evolution that occurs at or above the level of species, such as speciation, and microevolution, which is smaller evolutionary changes, such as adaptations, within a species or population. In general, macroevolution is the outcome of long periods of microevolution.[73] Thus, the distinction between micro- and macroevolution is not a fundamental one - the difference is simply the time involved.[74] However, in macroevolution, the traits of the entire species are important. For instance, a large amount of variation among individuals allows a species to rapidly adapt to new habitats, lessening the chance of it going extinct, while a wide geographic range increases the chance of speciation, by making it more likely that part of the population will become isolated. In this sense, microevolution and macroevolution can sometimes be separate.[75]
A common misconception is that evolution is "progressive," but natural selection has no long-term goal and does not necessarily produce greater complexity.[76] Although complex species have evolved, this occurs as a side effect of the overall number of organisms increasing, and simple forms of life remain more common.[77] For example, the overwhelming majority of species are microscopic prokaryotes, which form about half the world's biomass despite their small size,[78] and constitute the vast majority of Earth's biodiversity.[79] Simple organisms therefore remain the dominant form of life on Earth, and complex life appears more diverse only because it is more noticeable.[80]
Adaptation
- For more details on this topic, see Adaptation.
Adaptations are structures or behaviors that enhance a specific function, causing organisms to become better at surviving and reproducing.[5] They are produced by a combination of the continuous production of small, random changes in traits, followed by natural selection of the variants best-suited for their environment.[81] This process can cause either the gain of a new feature, or the loss of an ancestral feature. An example that shows both types of change is bacterial adaptation to antibiotic selection, with mutations causing antibiotic resistance by either modifying the target of the drug, or removing the transporters that allow the drug into the cell.[82] However, many traits that appear to be simple adaptations are in fact exaptations: structures originally adapted for one function, but which coincidentally became somewhat useful for some other function in the process.[83] One example is the African lizard Holapsis guentheri, which developed an extremely flat head for hiding in crevices, as can be seen by looking at its near relatives. However, in this species, the head has become so flattened that it assists in gliding from tree to tree - an exaptation.[83]
As adaptation occurs through the gradual modification of existing structures, structures with similar internal organization may have very different functions in related organisms. This is the result of a single ancestral structure being adapted to function in different ways. The bones within bat wings, for example, are structurally similar to both human hands and seal flippers, due to the common descent of these structures from an ancestor that also had five digits at the end of each forelimb. Other idiosyncratic anatomical features, such as bones in the wrist of the panda being formed into a false "thumb," indicate that an organism's evolutionary lineage can limit what adaptations are possible.[85]
During adaption, some structures may lose their original function and become vestigial structures.[86] Such structures may have little or no function in a current species, yet have a clear function in ancestral species, or other closely-related species. Examples include the non-functional remains of eyes in blind cave-dwelling fish,[87] wings in flightless birds,[88] and the presence of hip bones in whales and snakes.[89] Examples of vestigial structures in humans include wisdom teeth,[90] the coccyx,[86] and the vermiform appendix.[86]
An area of current investigation in evolutionary developmental biology is the developmental basis of adaptations and exaptations.[91] This research addresses the origin and evolution of embryonic development and how modifications of development and developmental processes produce novel features.[92] These studies have shown that evolution can alter development to create new structures, such as embryonic bone structures that develop into the jaw in other animals instead forming part of the middle ear in mammals.[93] It is also possible for structures that have been lost in evolution to reappear due to changes in developmental genes, such as a mutation in chickens causing embryos to grow teeth similar to those of crocodiles.[94]
Co-evolution
- For more details on this topic, see .
Co-operation
- For more details on this topic, see .
Coalitions between organisms of the same species have also evolved. An extreme case is the Eusociality found in social insects, such as bees, termites and ants, where sterile insects feed and guard the small number of organisms in a colony that are able to reproduce. On an even smaller scale, the somatic cells that make up the body of an animal are limited in their capacity to reproduce in order to maintain a stable organism which then supports a small number of the animal's germ cells to produce offspring. Here, somatic cells respond to specific signals that instruct them to either grow or kill themselves. If cells ignore these signals and attempt to multiply inappropriately, their uncontrolled growth causes cancer.[18]
These examples of cooperation within species are thought to have evolved through the process of kin selection, which is where one organism acts to help raise a relative's offspring.[100] This activity is selected for because if the helping individual contains alleles which promote the helping activity, it is likely that its kin will also contain these alleles and thus those alleles will be passed on.[101] Other processes that may promote cooperation include group selection, where cooperation provides benefits to a group of organisms.[102]
Speciation
- For more details on this topic, see .

The four mechanisms of speciation.
The second mechanism of speciation is peripatric speciation, which occurs when small populations of organisms become isolated in a new environment. This differs from allopatric speciation in that the isolated populations are numerically much smaller than the parental population. Here, the founder effect causes rapid speciation through both rapid genetic drift and selection on a small gene pool.[106]
The third mechanism of speciation is parapatric speciation. This is similar to peripatric speciation in that a small population enters a new habitat, but differs in that there is no physical separation between these two populations. Instead, speciation results from the evolution of mechanisms that reduce gene flow between the two populations.[103] Generally this occurs when there has been a drastic change in the environment within the parental species' habitat. One example is the grass Anthoxanthum odoratum, which can undergo parapatric speciation in response to localized metal pollution from mines.[107] Here, plants evolve that have resistance to high levels of metals in the soil. Selection against interbreeding with the metal-sensitive parental population produces a change in flowering time of the metal-resistant plants, causing reproductive isolation. Selection against hybrids between the two populations may cause reinforcement, which is the evolution of traits that promote mating within a species, as well as character displacement, which is when two species become more distinct in appearance.[108]
Finally, in sympatric speciation species diverge without geographic isolation or changes in habitat. This form is rare since even a small amount of gene flow may remove genetic differences between parts of a population.[109] Generally, sympatric speciation in animals requires the evolution of both genetic differences and non-random mating, to allow reproductive isolation to evolve.[110]
One type of sympatric speciation involves cross-breeding of two related species to produce a new hybrid species. This is not common in animals as animal hybrids are usually sterile, because during meiosis the homologous chromosomes from each parent, being from different species cannot successfully pair. It is more common in plants, however because plants often double their number of chromosomes, to form polyploids. This allows the chromosomes from each parental species to form a matching pair during meiosis, as each parent's chromosomes is represented by a pair already.[111]
Indeed, chromosome doubling can itself cause reproductive isolation, as half the doubled chromosomes will be unmatched when breeding with undoubled organisms.[112]
Speciation events are important in the theory of punctuated equilibrium, which accounts for the pattern in the fossil record of short "bursts" of evolution interspersed with relatively long periods of stasis, where species remain relatively unchanged.[113] In this theory, speciation and rapid evolution are linked, with natural selection and genetic drift acting most strongly on organisms undergoing speciation in novel habitats or small populations. As a result, the periods of stasis in the fossil record correspond to the parental population, and the organisms undergoing speciation and rapid evolution are found in small populations or geographically-restricted habitats, and therefore rarely being preserved as fossils.[114]
Extinction
- For more details on this topic, see .
A Tarbosaurus skeleton. Non-avian dinosaurs died out in the Cretaceous–Tertiary extinction event at the end of the Cretaceous period.
The role of extinction in evolution depends on which type is considered. The causes of the continuous "low-level" extinction events, which form the majority of extinctions, are not well understood and may be the result of competition between species for shared resources.[5] If competition from other species does alter the probability that a species will become extinct, this could produce species selection as a level of natural selection.[48] The intermittent mass extinctions are also important, but instead of acting as a selective force, they drastically reduce diversity in a nonspecific manner and promote bursts of rapid evolution and speciation in survivors.[117]
Evolutionary history of life
Origin of life
- For more details on this topic, see and .
Common descent
- For more details on this topic, see , , and .
The hominoids are descendants of a common ancestor.
Past species have also left records of their evolutionary history. Fossils, along with the comparative anatomy of present-day organisms, constitute the morphological, or anatomical, record.[129] By comparing the anatomies of both modern and extinct species, paleontologists can infer the lineages of those species. However, this approach is most successful for organisms that had hard body parts, such as shells, bones or teeth. Further, as prokaryotes such as bacteria and archaea share a limited set of common morphologies, their fossils do not provide information on their ancestry.
More recently, evidence for common descent has come from the study of biochemical similarities between organisms. For example, all living cells use the same nucleic acids and amino acids.[130] The development of molecular genetics has revealed the record of evolution left in organisms' genomes: dating when species diverged through the molecular clock produced by mutations.[131] For example, these DNA sequence comparisons have revealed the close genetic similarity between humans and chimpanzees and shed light on when the common ancestor of these species existed.[132]

Evolutionary tree showing the divergence of modern species from their common ancestor in the center.[133] The three domains are colored, with bacteria blue, archaea green, and eukaryotes red.
Evolution of life
- For more details on this topic, see Timeline of evolution.
The eukaryotes were the next major innovation in evolution. These came from ancient bacteria being engulfed by the ancestors of eukaryotic cells, in a cooperative association called endosymbiosis.[137][138] The engulfed bacteria and the host cell then underwent co-evolution, with the bacteria evolving into either mitochondria or hydrogenosomes.[139] An independent second engulfment of cyanobacterial-like organisms led to the formation of chloroplasts in algae and plants.[140]
The history of life was that of the unicellular eukaryotes, prokaryotes, and archaea until about a billion years ago when multicellular organisms began to appear in the oceans in the Ediacaran period.[134][141] The evolution of multicellularity occurred in multiple independent events, in organisms as diverse as sponges, brown algae, cyanobacteria, slime moulds and myxobacteria.[142]
Soon after the emergence of these first multicellular organisms, a remarkable amount of biological diversity appeared over approximately 10 million years, in an event called the Cambrian explosion. Here, the majority of types of modern animals evolved, as well as unique lineages that subsequently became extinct.[143] Various triggers for the Cambrian explosion have been proposed, including the accumulation of oxygen in the atmosphere from photosynthesis.[144] About 500 million years ago, plants and fungi colonized the land, and were soon followed by arthropods and other animals.[145] Amphibians first appeared around 300 million years ago, followed by early amniotes, then mammals around 200 million years ago and birds around 100 million years ago (both from "reptile"-like lineages). However, despite the evolution of these large animals, smaller organisms similar to the types that evolved early in this process continue to be highly successful and dominate the Earth, with the majority of both biomass and species being prokaryotes.[79]
History of evolutionary thought
Charles Darwin at age 51, just after publishing The Origin of Species.
- For more details on this topic, see History of evolutionary thought.
Evolutionary ideas such as common descent and the transmutation of species have existed since at least the 6th century BC, when they were expounded by the Greek philosopher Anaximander.[146] Evolutionary thought was further developed by other early thinkers, including the Greek philosopher Empedocles, the Roman philosopher Lucretius, the Arab biologist Al-Jahiz,[147] the Persian philosopher Ibn Miskawayh, and the Brethren of Purity.[148] Also in the Far East, the philosopher Zhuangzi discussed a transformative power of species to adapt to their surroundings. [149] As biological knowledge grew in the 18th century, a variety of such ideas developed, beginning with Pierre Maupertuis in 1745, and with contributions from natural philosophers such as Erasmus Darwin and Jean-Baptiste Lamarck.[150] In 1858, Charles Darwin and Alfred Russel Wallace jointly proposed the theory of evolution by natural selection to the Linnean Society of London in separate papers.[151] Shortly after, Darwin's publication of The Origin of Species provided detailed support for the theory and led to increasingly wide acceptance of the occurrence of evolution.
Nonetheless, Darwin's specific ideas about evolution, such as gradualism and the mechanisms of natural selection, were strongly contested at first. Lamarckists argued that transmutation of species occurred as parents passed on adaptations acquired during their lifetimes.[152] Eventually, when experiments failed to support it, this idea was abandoned in favor of Darwinism.[153] More significantly, Darwin could not account for how traits were passed down from generation to generation. A mechanism was provided in 1865 by Gregor Mendel, who found that traits were inherited in a predictable manner.[154] When Mendel's work was rediscovered in 1900, disagreements over the rate of evolution predicted by early geneticists and biometricians led to a rift between the Mendelian and Darwinian models of evolution.

Gregor Mendel, who laid the foundation for genetics.
In its early history, evolutionary biology primarily drew in scientists from traditional taxonomically-oriented disciplines, whose specialist training in particular organisms addressed general questions in evolution. As evolutionary biology expanded as an academic discipline, particularly after the development of the modern evolutionary synthesis, it began to draw more widely from the biological sciences.[5] Currently the study of evolutionary biology involves scientists from fields as diverse as biochemistry, ecology, genetics and physiology, and evolutionary concepts are used in even more distant disciplines such as psychology, medicine, philosophy and computer science.
Social and religious controversies
- For more details on this topic, see , , and .
Caricature of Charles Darwin as an ape, reflecting the cultural backlash against evolution.
Even before the publication of The Origin of Species, the idea that life had evolved was a source of controversy and evolution is still the subject of contention. Debate has generally centered on the philosophical, social and religious implications of evolution, not on the science itself; the proposition that biological evolution occurs through the mechanism of natural selection is completely uncontested in the scientific literature.[157]
As Darwin recognized early on, the most controversial aspect of evolutionary thought is its application to humans. Specifically, some people object to the idea that humans arose through natural processes without supernatural intervention. Although many religions and denominations have reconciled their beliefs with evolution through theistic evolution, several denominations contain creationists who object to evolution, as it contradicts their literal interpretation of origin beliefs.[158] In some countries – notably the United States – these tensions between scientific and religious teachings have fueled the ongoing creation–evolution controversy, a religious conflict focusing on politics and public education.[159] While other scientific fields such as cosmology[160] and earth science[161] also conflict with literal interpretations of many religious texts, evolutionary biology has borne the brunt of religious objection.
Evolution has also attracted controversy because it has been used to support philosophical positions that promote discrimination and racism. For example, the eugenic ideas of Francis Galton were developed into arguments that the human gene pool should be improved by selective breeding policies, including incentives for those considered "good stock" to reproduce, and the compulsory sterilization, prenatal testing, birth control, and even killing, of those considered bad stock.[162] Another example of an extension of evolutionary theory that is now widely regarded as unwarranted is "Social Darwinism," a term given to the 19th century Whig Malthusian theory developed by Herbert Spencer into ideas about "survival of the fittest" in commerce and human societies as a whole, and by others into claims that social inequality, racism, and imperialism were justified.[163] However, contemporary scientists and philosophers consider these ideas to have been neither mandated by evolutionary theory nor supported by data.[164][165]
Uses in technology
- For more details on this topic, see and .
A major technological application of the power of evolution is artificial selection, which is the intentional selection of certain traits in a population of organisms. Humans have used artificial selection for thousands of years in the domestication of plants and animals.[166] More recently, such selection has become a vital part of genetic engineering, with selectable markers such as antibiotic resistance genes being used to manipulate DNA in molecular biology.
As evolution can produce highly optimized processes and networks, it has many applications in computer science. Here, simulations of evolution using evolutionary algorithms and artificial life started with the work of Nils Aall Barricelli in the 1960s, and was extended by Alex Fraser, who published a series of papers on simulation of artificial selection.[167] Artificial evolution became a widely recognized optimization method as a result of the work of Ingo Rechenberg in the 1960s and early 1970s, who used evolution strategies to solve complex engineering problems.[168] Genetic algorithms in particular became popular through the writing of John Holland.[169] As academic interest grew, dramatic increases in the power of computers allowed practical applications. Evolution algorithms are now used to solve multi-dimensional problems more quickly than software produced by human designers, and also to optimize the design of systems.[170]
Further reading
Introductory reading- Jones S (2001). Almost Like a Whale: The Origin of Species Updated. (American title: Darwin's Ghost). New York: Ballantine Books. ISBN 0-345-42277-5.
- Dawkins R (2006). The Selfish Gene: 30th Anniversary Edition. Oxford University Press. ISBN 0199291152.
- Charlesworth CB, Charlesworth D (2003). Evolution. Oxfordshire: Oxford University Press. ISBN 0-192-80251-8.
- Gould, Stephen Jay (1989). Wonderful Life: The Burgess Shale and the Nature of History. New York: W.W. Norton. ISBN 0-393-30700-X.
- Carroll S (2005). Endless Forms Most Beautiful. New York: W.W. Norton. ISBN 0-393-06016-0.
- Smith, Cameron B. and Charles Sullivan (2007). The Top 10 Myths about Evolution. Prometheus Books. ISBN 978-1-59102-479-8.
- Larson EJ (2004). Evolution: The Remarkable History of a Scientific Theory. New York: Modern Library. ISBN 0-679-64288-9.
- Zimmer C (2001). Evolution: The Triumph of an Idea. London: HarperCollins. ISBN 0-060-19906-7.
- Gould, Stephen Jay (2002). The Structure of Evolutionary Theory. Cambridge: Belknap Press (Harvard University Press). ISBN 0-674-00613-5.
- Futuyma DJ (2005). Evolution. Sunderland: Sinauer Associates. ISBN 0-878-93187-2.
- Mayr E (2001). What Evolution Is. New York: Basic Books. ISBN 0-465-04426-3.
- Coyne JA, Orr HA (2004). Speciation. Sunderland: Sinauer Associates. ISBN 0-878-93089-2.
- Smith JM, Szathmáry E (1997). The Major Transitions in Evolution. Oxfordshire: Oxford University Press. ISBN 0-198-50294-X.
- Nicholas H. Barton, Derek E.G. Briggs, Jonathan A. Eisen, David B. Goldstein and Nipam H. Patel (2007). Evolution. Cold Spring Harbor Laboratory Press. ISBN 0-879-69684-2.
External links
General information- Understanding Evolution from University of California, Berkeley
- National Academies Evolution Resources
- Everything you wanted to know about evolution by New Scientist
- Howstuffworks.com — How Evolution Works
- Synthetic Theory Of Evolution: An Introduction to Modern Evolutionary Concepts and Theories
- The Complete Work of Charles Darwin Online
- Understanding Evolution: History, Theory, Evidence, and Implications
Basic topics in |
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Evidence of evolution
Processes of evolution: adaptation - macroevolution - microevolution - speciation
Population genetic mechanisms: natural selection - genetic drift - gene flow - mutation
Evolutionary developmental biology (Evo-devo) concepts: phenotypic plasticity - canalisation - modularity
Modes of evolution: anagenesis - catagenesis - cladogenesis
History: History of evolutionary thought - Charles Darwin - The Origin of Species - modern evolutionary synthesis - Evolutionary history of life
Other subfields: ecological genetics - human evolution - molecular evolution - phylogenetics - systematics
List of evolutionary biology topics - Timeline of evolution
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References
1. ^ Lande R, Arnold SJ (1983). "The measurement of selection on correlated characters". Evolution 37: 1210–26} |doi=10.2307/2408842.
2. ^ Ayala FJ (2007). "Darwin's greatest discovery: design without designer". Proc. Natl. Acad. Sci. U.S.A. 104 Suppl 1: 8567–73. PMID 17494753.
3. ^
4. ^ Futuyma, Douglas J. (2005). Evolution. Sunderland, Massachusetts: Sinauer Associates, Inc. ISBN 0-87893-187-2.
5. ^ Darwin, Charles (1859). On the Origin of Species, 1st, John Murray, p. 1. . Related earlier ideas were acknowledged in Darwin, Charles (1861). On the Origin of Species, 3rd, John Murray, p. xiii.
6. ^ IAP Statement on the Teaching of Evolution. The Interacademy Panel on International Issues (2006). Retrieved on 2007-04-25.—Statement on the Teaching of Evolution. American Association for the Advancement of Science (2006). Retrieved on 2007-04-25.
7. ^ Sturm RA, Frudakis TN (2004). "Eye colour: portals into pigmentation genes and ancestry". Trends Genet. 20 (8): 327–32. PMID 15262401.
8. ^ Pearson H (2006). "Genetics: what is a gene?". Nature 441 (7092): 398–401. PMID 16724031.
9. ^ Peaston AE, Whitelaw E (2006). "Epigenetics and phenotypic variation in mammals". Mamm. Genome 17 (5): 365–74. PMID 16688527.
10. ^ Oetting WS, Brilliant MH, King RA (1996). "The clinical spectrum of albinism in humans". Molecular medicine today 2 (8): 330–35. PMID 8796918.
11. ^ Mayeux R (2005). "Mapping the new frontier: complex genetic disorders". J. Clin. Invest. 115 (6): 1404–07. PMID 15931374.
12. ^ Wu R, Lin M (2006). "Functional mapping - how to map and study the genetic architecture of dynamic complex traits". Nat. Rev. Genet. 7 (3): 229–37. PMID 16485021.
13. ^ Stoltzfus A (2006). "Mutationism and the dual causation of evolutionary change". Evol. Dev. 8 (3): 304–17. PMID 16686641.
14. ^ Harwood AJ (1998). "Factors affecting levels of genetic diversity in natural populations". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 353 (1366): 177–86. PMID 9533122.
15. ^ Draghi J, Turner P (2006). "DNA secretion and gene-level selection in bacteria". Microbiology (Reading, Engl.) 152 (Pt 9): 2683–8. PMID 16946263.
*Mallet J (2007). "Hybrid speciation". Nature 446 (7133): 279–83. PMID 17361174. ,
16. ^ Butlin RK, Tregenza T (1998). "Levels of genetic polymorphism: marker loci versus quantitative traits". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 353 (1366): 187–98. PMID 9533123.
17. ^ Wetterbom A, Sevov M, Cavelier L, Bergström TF (2006). "Comparative genomic analysis of human and chimpanzee indicates a key role for indels in primate evolution". J. Mol. Evol. 63 (5): 682–90. PMID 17075697.
18. ^ Bertram J (2000). "The molecular biology of cancer". Mol. Aspects Med. 21 (6): 167–223. PMID 11173079.
19. ^ Aminetzach YT, Macpherson JM, Petrov DA (2005). "Pesticide resistance via transposition-mediated adaptive gene truncation in Drosophila". Science 309 (5735): 764–67. DOI:10.1126/science.1112699. PMID 16051794.
20. ^ Burrus V, Waldor M (2004). "Shaping bacterial genomes with integrative and conjugative elements". Res. Microbiol. 155 (5): 376–86. PMID 15207870.
21. ^ Sawyer SA, Parsch J, Zhang Z, Hartl DL (2007). "Prevalence of positive selection among nearly neutral amino acid replacements in Drosophila". Proc. Natl. Acad. Sci. U.S.A. 104 (16): 6504-10. PMID 17409186.
22. ^ Sniegowski P, Gerrish P, Johnson T, Shaver A (2000). "The evolution of mutation rates: separating causes from consequences". Bioessays 22 (12): 1057–66. PMID 11084621.
23. ^ Carroll SB, Grenier J, Weatherbee SD (2005). From DNA to Diversity: Molecular Genetics and the Evolution of Animal Design. Second Edition. Oxford: Blackwell Publishing. ISBN 1-4051-1950-0.
24. ^ Harrison P, Gerstein M (2002). "Studying genomes through the aeons: protein families, pseudogenes and proteome evolution". J Mol Biol 318 (5): 1155–74. PMID 12083509.
25. ^ Orengo CA, Thornton JM (2005). "Protein families and their evolution-a structural perspective". Annu. Rev. Biochem. 74: 867–900. PMID 15954844.
26. ^ Pál C, Papp B, Lercher MJ (2006). "An integrated view of protein evolution". Nat. Rev. Genet. 7 (5): 337–48. PMID 16619049.
27. ^ Bowmaker JK (1998). "Evolution of colour vision in vertebrates". Eye (London, England) 12 (Pt 3b): 541–47. PMID 9775215.
28. ^ Gregory TR, Hebert PD (1999). "The modulation of DNA content: proximate causes and ultimate consequences". Genome Res. 9 (4): 317–24. PMID 10207154.
29. ^ Zhang J, Wang X, Podlaha O (2004). "Testing the chromosomal speciation hypothesis for humans and chimpanzees". Genome Res. 14 (5): 845–51. PMID 15123584.
30. ^ Ayala FJ, Coluzzi M (2005). "Chromosome speciation: humans, Drosophila, and mosquitoes". Proc. Natl. Acad. Sci. U.S.A. 102 Suppl 1: 6535–42. PMID 15851677.
31. ^ Hurst GD, Werren JH (2001). "The role of selfish genetic elements in eukaryotic evolution". Nat. Rev. Genet. 2 (8): 597–606. PMID 11483984.
32. ^ Häsler J, Strub K (2006). "Alu elements as regulators of gene expression". Nucleic Acids Res. 34 (19): 5491–97. PMID 17020921.
33. ^ Aminetzach YT, Macpherson JM, Petrov DA (2005). "Pesticide resistance via transposition-mediated adaptive gene truncation in Drosophila". Science 309 (5735): 764–67. PMID 16051794.
34. ^ Radding C (1982). "Homologous pairing and strand exchange in genetic recombination". Annu. Rev. Genet. 16: 405–37. PMID 6297377.
35. ^ Lien S, Szyda J, Schechinger B, Rappold G, Arnheim N (2000). "Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping". Am. J. Hum. Genet. 66 (2): 557–66. PMID 10677316.
36. ^ Sabeti P, Schaffner S, Fry B, Lohmueller J, Varilly P, Shamovsky O, Palma A, Mikkelsen T, Altshuler D, Lander E (2006). "Positive natural selection in the human lineage". Science 312 (5780): 1614–20. PMID 16778047.
37. ^ Otto S (2003). "The advantages of segregation and the evo
2. ^ Ayala FJ (2007). "Darwin's greatest discovery: design without designer". Proc. Natl. Acad. Sci. U.S.A. 104 Suppl 1: 8567–73. PMID 17494753.
3. ^
4. ^ Futuyma, Douglas J. (2005). Evolution. Sunderland, Massachusetts: Sinauer Associates, Inc. ISBN 0-87893-187-2.
5. ^ Darwin, Charles (1859). On the Origin of Species, 1st, John Murray, p. 1. . Related earlier ideas were acknowledged in Darwin, Charles (1861). On the Origin of Species, 3rd, John Murray, p. xiii.
6. ^ IAP Statement on the Teaching of Evolution. The Interacademy Panel on International Issues (2006). Retrieved on 2007-04-25.—Statement on the Teaching of Evolution. American Association for the Advancement of Science (2006). Retrieved on 2007-04-25.
7. ^ Sturm RA, Frudakis TN (2004). "Eye colour: portals into pigmentation genes and ancestry". Trends Genet. 20 (8): 327–32. PMID 15262401.
8. ^ Pearson H (2006). "Genetics: what is a gene?". Nature 441 (7092): 398–401. PMID 16724031.
9. ^ Peaston AE, Whitelaw E (2006). "Epigenetics and phenotypic variation in mammals". Mamm. Genome 17 (5): 365–74. PMID 16688527.
10. ^ Oetting WS, Brilliant MH, King RA (1996). "The clinical spectrum of albinism in humans". Molecular medicine today 2 (8): 330–35. PMID 8796918.
11. ^ Mayeux R (2005). "Mapping the new frontier: complex genetic disorders". J. Clin. Invest. 115 (6): 1404–07. PMID 15931374.
12. ^ Wu R, Lin M (2006). "Functional mapping - how to map and study the genetic architecture of dynamic complex traits". Nat. Rev. Genet. 7 (3): 229–37. PMID 16485021.
13. ^ Stoltzfus A (2006). "Mutationism and the dual causation of evolutionary change". Evol. Dev. 8 (3): 304–17. PMID 16686641.
14. ^ Harwood AJ (1998). "Factors affecting levels of genetic diversity in natural populations". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 353 (1366): 177–86. PMID 9533122.
15. ^ Draghi J, Turner P (2006). "DNA secretion and gene-level selection in bacteria". Microbiology (Reading, Engl.) 152 (Pt 9): 2683–8. PMID 16946263.
*Mallet J (2007). "Hybrid speciation". Nature 446 (7133): 279–83. PMID 17361174. ,
16. ^ Butlin RK, Tregenza T (1998). "Levels of genetic polymorphism: marker loci versus quantitative traits". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 353 (1366): 187–98. PMID 9533123.
17. ^ Wetterbom A, Sevov M, Cavelier L, Bergström TF (2006). "Comparative genomic analysis of human and chimpanzee indicates a key role for indels in primate evolution". J. Mol. Evol. 63 (5): 682–90. PMID 17075697.
18. ^ Bertram J (2000). "The molecular biology of cancer". Mol. Aspects Med. 21 (6): 167–223. PMID 11173079.
19. ^ Aminetzach YT, Macpherson JM, Petrov DA (2005). "Pesticide resistance via transposition-mediated adaptive gene truncation in Drosophila". Science 309 (5735): 764–67. DOI:10.1126/science.1112699. PMID 16051794.
20. ^ Burrus V, Waldor M (2004). "Shaping bacterial genomes with integrative and conjugative elements". Res. Microbiol. 155 (5): 376–86. PMID 15207870.
21. ^ Sawyer SA, Parsch J, Zhang Z, Hartl DL (2007). "Prevalence of positive selection among nearly neutral amino acid replacements in Drosophila". Proc. Natl. Acad. Sci. U.S.A. 104 (16): 6504-10. PMID 17409186.
22. ^ Sniegowski P, Gerrish P, Johnson T, Shaver A (2000). "The evolution of mutation rates: separating causes from consequences". Bioessays 22 (12): 1057–66. PMID 11084621.
23. ^ Carroll SB, Grenier J, Weatherbee SD (2005). From DNA to Diversity: Molecular Genetics and the Evolution of Animal Design. Second Edition. Oxford: Blackwell Publishing. ISBN 1-4051-1950-0.
24. ^ Harrison P, Gerstein M (2002). "Studying genomes through the aeons: protein families, pseudogenes and proteome evolution". J Mol Biol 318 (5): 1155–74. PMID 12083509.
25. ^ Orengo CA, Thornton JM (2005). "Protein families and their evolution-a structural perspective". Annu. Rev. Biochem. 74: 867–900. PMID 15954844.
26. ^ Pál C, Papp B, Lercher MJ (2006). "An integrated view of protein evolution". Nat. Rev. Genet. 7 (5): 337–48. PMID 16619049.
27. ^ Bowmaker JK (1998). "Evolution of colour vision in vertebrates". Eye (London, England) 12 (Pt 3b): 541–47. PMID 9775215.
28. ^ Gregory TR, Hebert PD (1999). "The modulation of DNA content: proximate causes and ultimate consequences". Genome Res. 9 (4): 317–24. PMID 10207154.
29. ^ Zhang J, Wang X, Podlaha O (2004). "Testing the chromosomal speciation hypothesis for humans and chimpanzees". Genome Res. 14 (5): 845–51. PMID 15123584.
30. ^ Ayala FJ, Coluzzi M (2005). "Chromosome speciation: humans, Drosophila, and mosquitoes". Proc. Natl. Acad. Sci. U.S.A. 102 Suppl 1: 6535–42. PMID 15851677.
31. ^ Hurst GD, Werren JH (2001). "The role of selfish genetic elements in eukaryotic evolution". Nat. Rev. Genet. 2 (8): 597–606. PMID 11483984.
32. ^ Häsler J, Strub K (2006). "Alu elements as regulators of gene expression". Nucleic Acids Res. 34 (19): 5491–97. PMID 17020921.
33. ^ Aminetzach YT, Macpherson JM, Petrov DA (2005). "Pesticide resistance via transposition-mediated adaptive gene truncation in Drosophila". Science 309 (5735): 764–67. PMID 16051794.
34. ^ Radding C (1982). "Homologous pairing and strand exchange in genetic recombination". Annu. Rev. Genet. 16: 405–37. PMID 6297377.
35. ^ Lien S, Szyda J, Schechinger B, Rappold G, Arnheim N (2000). "Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping". Am. J. Hum. Genet. 66 (2): 557–66. PMID 10677316.
36. ^ Sabeti P, Schaffner S, Fry B, Lohmueller J, Varilly P, Shamovsky O, Palma A, Mikkelsen T, Altshuler D, Lander E (2006). "Positive natural selection in the human lineage". Science 312 (5780): 1614–20. PMID 16778047.
37. ^ Otto S (2003). "The advantages of segregation and the evo

