Wikipedia

Macroevolution

(Redirected from Macro evolution)

Macroevolution comprises the evolutionary processes and patterns which occur at and above the species level.[1][2][3] In contrast, microevolution is evolution occurring within the population(s) of a single species. In other words, microevolution is the scale of evolution that is limited to intraspecific (within-species) variation, while macroevolution extends to interspecific (between-species) variation.[4] The evolution of new species (speciation) is an example of macroevolution. This is the common definition for 'macroevolution' used by contemporary scientists.[a][b][c][d][e][f][g][h][i] Although, the exact usage of the term has varied throughout history.[4][10][11]

Macroevolution addresses the evolution of species and higher taxonomic groups (genera, families, orders, etc) and uses evidence from phylogenetics,[5] the fossil record,[9] and molecular biology to answer how different taxonomic groups exhibit different species diversity and/or morphological disparity.[12]

Origin and changing meaning of the term

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After Charles Darwin published his book On the Origin of Species[13] in 1859, evolution was widely accepted to be real phenomenon. However, many scientists still disagreed with Darwin that natural selection was the primary mechanism to explain evolution. Prior to the Modern Synthesis, during the period between the 1880s to the 1930s (dubbed the ‘Eclipse of Darwinism’) many scientists argued in favor of alternative explanations. These included ‘orthogenesis’, and among its proponents was the Russian entomologist Yuri A. Filipchenko.

Filipchenko appears to have been the one who coined the term ‘macroevolution’ in his book Variabilität und Variation (1927).[11] While introducing the concept, he claimed that the field of genetics is insufficient to explain “the origin of higher systematic units” above the species level.

Auf die Weise hebt die heutige Genetik zweifellos den Schleier von der Evolution der Biotypen, Jordanone und Linneone (eine Art Mikroevolution), dagegen jene Evolution der höheren systematischen Gruppen, welche von jeher die Geister besonders für sich in Anspruch genommen hat (eine Art Makroevolution), liegt gänzlich außerhalb ihres Gesichtsfeldes, und dieser Umstand scheint uns die von uns oben angeführten Erwägungen über das Fehlen einer inneren Beziehung zwischen der Genetik und der Deszendenzlehre, die sich ja hauptsächlich mit der Makroevolution befaßt, nur zu unterstreichen.

Bei einer solchen Sachlage muß zugegeben werden, daß die Entscheidung der Frage über die Faktoren der größeren Züge der Evolution, d. h. dessen, was wir Makroevolution nennen, unabhängig von den Ergebnissen der gegenwärtigen Genetik geschehen muß. So vorteilhaft es für uns auch wäre, uns auch in dieser Frage auf die exakten Resultate der Genetik zu stützen, so sind sie doch, unserer Meinung nach, zu diesem Zweck ganz unbrauchbar, da die Frage über die Entstehung der höheren systematischen Einheiten ganz außerhalb des Forschungsgebietes der Genetik liegt. Infolgedessen ist letztere auch eine exakte Wissenschaft, während die Dezendenzlehre heute, ebenso wie auch in XIX. Jahrhundert, einen einen spekulativen Charakter trägt.

In this way, modern genetics undoubtedly lifts the veil from the evolution of biotypes, Jordanones and Linneones [i.e. variations within a species][j] (a kind of microevolution), but that evolution of the higher systematic groups, which has always particularly occupied the minds of men (a kind of macroevolution), lies entirely outside its field of vision, and this circumstance seems to us only to emphasize the considerations we have given above about the lack of an inner relationship between genetics and the theory of descent, which is mainly concerned with macroevolution.

In such a state of affairs, it must be admitted that the decision of the question depends on the factors of the larger features of evolution, of what we call macroevolution, must occur independently of the results of current genetics. As advantageous as it would be for us to rely on the exact results of genetics in this question, they are, in our opinion, completely useless for this purpose, since the question about the origin of the higher systematic units lies entirely outside the field research area of genetics. As a result, the latter is also an exact science, while the doctrine of descent today, as well as in the 19th century, has a speculative character.

— Yuri Filipchenko, Variabilität und Variation (1927), pages 93-94[11]

Regarding the origin of higher systematic units, Filipchenko stated his claim that ‘like-produces-like’. A taxon must originate from other taxa of equivalent rank. A new species must come from an old species, a genus from an older genus, a family from another family, etc.

Hier scheint uns ein wesentliches Mißverständnis obzuwalten. Davon schon gar nicht zu reden, daß es kaum richtig ist, in den Jardanonen Spaltungsprodukte eines Linneone zu sehen, ist es noch unrichtiger anzunehmen, daß nach den heutigen Anschauungen ein Jordanon sich im Evolutionsprozeß in ein neues Linneon verwandeln kann oder muß. Im Gegenteil, uns scheint, daß sich bei der Evolution die verschiedenen taxonomischen Einheiten so verhalten, daß Gleiches Gleiches erzeugt. Aus einem Biotyp entsteht durch Mutation ein neuer Biotypus, aus einem Jordanon bildet sich - durch eine Neugruppierung der ihn bildenden Biotypen, sowie durch das Auftreten einiger neuer - ein zweites Jordanon; endlich zerfällt ein aus mehreren Jordanonen bestehendes Linneon infolge des Verschwindens einiger von ihnen in zwei selbständige Linneone. Es ist vollkommen richtig, daß niemand eine Umwandlung der Rassen in eine Art beobachtet hat, aber das braucht auch nicht zu sein, da im Prozeß der Evolution eine neue Art oder Arten gewöhnlich aus einer alten Art, eine neue Gattung aus einer anderen Gattung usw. entstehen.
There seems to be a fundamental misunderstanding here. Not to mention that it is hardly correct to see the Jardanones[j] as products of the fission of a Linneone,[j] it is even more incorrect to assume that, according to modern views, a Jordanone can or must transform into a new Linneone in the process of evolution. On the contrary, it seems to us that in evolution the various taxonomic units behave in such a way that like produces like. A new biotype[j] arises from one biotype through mutation; a Jordanone forms a second Jordanone through a regrouping of the biotypes that make up it and the appearance of some new ones; finally, a Linneone consisting of several Jordanones splits into two independent Linneones as a result of the disappearance of some of them. It is quite true that no one has observed a transformation of the races into a species, but that need not be the case, since in the process of evolution a new species or species usually arise from an old species, a new genus from another genus, etc.

— Yuri Filipchenko, Variabilität und Variation (1927), page 89 [11]

Filipchenko believed this was the only way to explain the origin of the major characters that define species and especially higher taxonomic groups (genera, families, orders, etc). For example, the origin of families must require the sudden appearance of new traits which are different in greater magnitude compared to the characters required for the origin of a genus or species. However, this view is no longer consistent with contemporary understanding of evolution. Furthermore, the Linnaean ranks of ‘genus’ (and higher) are not real entities but artificial concepts which break down when they are combined with the process of evolution.[15][10]

Nevertheless, Filipchenko’s distinction between microevolution and macroevolution had a major impact on the development of evolutionary science. The term was adopted by Filipchenko's protégé Theodosius Dobzhansky in his book ‘Genetics und the Origin of Species’ (1937), a seminal piece that contributed to the development of the Modern Synthesis. ‘Macroevolution’ was also adopted by those who used it to criticize the Modern Synthesis. A notable example of this was the book The Material Basis of Evolution (1940) by the geneticist Richard Goldschmidt, a close friend of Filipchenko.[16] Goldschmidt suggested saltational evolutionary changes either due to mutations that affect the rates of developmental processes[17] or due to alterations in the chromosomal pattern.[18] Particularly the latter idea was widely rejected by the modern synthesis, but the hopeful monster concept based on Evolutionary developmental biology (or evo-devo) explanations found a moderate revival in recent times.[19][20] Occasionally such dramatic changes can lead to novel features that survive.

As an alternative to saltational evolution, Dobzhansky[21] suggested that the difference between macroevolution and microevolution reflects essentially a difference in time-scales, and that macroevolutionary changes were simply the sum of microevolutionary changes over geologic time. This view became broadly accepted, and accordingly, the term macroevolution has been used widely as a neutral label for the study of evolutionary changes that take place over a very large time-scale.[22] Further, species selection[2] suggests that selection among species is a major evolutionary factor that is independent from and complementary to selection among organisms. Accordingly, the level of selection has become the conceptual basis of a third definition, which defines macroevolution as evolution through selection among interspecific variation.[4]

Microevolution vs Macroevolution

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The fact that both micro- and macroevolution (including common descent) are supported by overwhelming evidence remains uncontroversial within the scientific community. However, there has been considerable debate over the past 80 years regarding causal and explanatory connection between microevolution and macroevolution.[1]

The ‘Extrapolation’ view holds there is no fundamental difference between the two aside from scale; i.e. macroevolution is merely cumulative microevolution. Hence, the patterns observed at the macroevolutionary scale can be explained by microevolutionary processes over long periods of time.

The ‘Decoupled’ view holds that microevolutionary processes are decoupled from macroevolutionary processes because there are separate macroevolutionary processes that cannot be sufficiently explained by microevolutionary processes alone.

" ... macroevolutionary processes are underlain by microevolutionary phenomena and are compatible with microevolutionary theories, but macroevolutionary studies require the formulation of autonomous hypotheses and models (which must be tested using macroevolutionary evidence). In this (epistemologically) very important sense, macroevolution is decoupled from microevolution: macroevolution is an autonomous field of evolutionary study."                           Francisco J. Ayala (1983)[23]

Many scientists see macroevolution as a field of study rather than a distinct process that is similar to the process of microevolution. Thus, macroevolution is concerned with the history of life and macroevolutionary explanations encompasses ecology, paleontology, mass extinctions, plate tectonics, and unique events such as the Cambrian explosion.[24][5][25][26][16][10][27]

Within microevolution, the evolutionary process of changing heritable characteristics (e.g. changes in allele frequencies) is described by population genetics, with mechanisms such as mutation, natural selection, and genetic drift. However, the scope of evolution can be expanded to higher scales where different observations are made. Macroevolutionary mechanisms are provided to explain these.[2] For example, speciation can be discussed in terms of the ‘mode’, i.e. how speciation occurs. Different modes of speciation include sympatric and allopatric). Additionally, scientists research the 'tempo' of speciation, i.e. the rate at which species change genetically and/or morphologically. Classically, competing hypothesis for the tempo of specieation include phyletic gradualism and punctuated equilibrium). Lastly, what are the causes of speciation is also extensively researched.[1]

More questions can be asked regarding the evolution of species and higher taxonomic groups (genera, families, orders, etc), and how these have evolved across geography and vast spans of geological time. Such questions are researched from various fields of science. This makes the study of 'macroevolution' interdisciplinary. For example:

Macroevolutionary processes

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Speciation

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Main article: speciation

According to the modern definition, the evolutionary transition from the ancestral to the daughter species is microevolutionary, because it results from selection (or, more generally, sorting) among varying organisms. However, speciation has also a macroevolutionary aspect, because it produces the interspecific variation species selection operates on.[4] Another macroevolutionary aspect of speciation is the rate at which it successfully occurs, analogous to reproductive success in microevolution.[2]

Speciation is the process in which populations within one species change to an extent at which they become reproductively isolated, that is, they cannot interbreed anymore. However, this classical concept has been challenged and more recently, a phylogenetic or evolutionary species concept has been adopted. Their main criteria for new species is to be diagnosable and monophyletic, that is, they form a clearly defined lineage.[29][30]

Charles Darwin first discovered that speciation can be extrapolated so that species not only evolve into new species, but also into new genera, families and other groups of animals. In other words, macroevolution is reducible to microevolution through selection of traits over long periods of time.[31] In addition, some scholars have argued that selection at the species level is important as well.[32] The advent of genome sequencing enabled the discovery of gradual genetic changes both during speciation but also across higher taxa. For instance, the evolution of humans from ancestral primates or other mammals can be traced to numerous but individual mutations.[33]

Evolution of new organs and tissues

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One of the main questions in evolutionary biology is how new structures evolve, such as new organs. Macroevolution is often thought to require the evolution of structures that are 'completely new'. However, fundamentally novel structures are not necessary for dramatic evolutionary change. As can be seen in vertebrate evolution, most "new" organs are actually not new—they are simply modifications of previously existing organs. For instance, the evolution of mammal diversity in the past 100 million years has not required any major innovation.[34] All of this diversity can be explained by modification of existing organs, such as the evolution of elephant tusks from incisors. Other examples include wings (modified limbs), feathers (modified reptile scales),[35] lungs (modified swim bladders, e.g. found in fish),[36][37] or even the heart (a muscularized segment of a vein).[38]

The same concept applies to the evolution of "novel" tissues. Even fundamental tissues such as bone can evolve from combining existing proteins (collagen) with calcium phosphate (specifically, hydroxy-apatite). This probably happened when certain cells that make collagen also accumulated calcium phosphate to get a proto-bone cell.[39]

Molecular macroevolution

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Microevolution is facilitated by mutations, the vast majority of which have no or very small effects on gene or protein function. For instance, the activity of an enzyme may be slightly changed or the stability of a protein slightly altered. However, occasionally mutations can dramatically change the structure and functions of protein. This may be called "molecular macroevolution".

 
The metabolic enzyme galactokinase can be converted to a transcription factor (in yeast) by just a 2 amino-acid insertion.

Protein function. There are countless cases in which protein function is dramatically altered by mutations. For instance, a mutation in acetaldehyde dehydrogenase (EC:1.2.1.10) can change it to a 4-hydroxy-2-oxopentanoate pyruvate lyase (EC:4.1.3.39), i.e., a mutation that changes an enzyme from one to another EC class (there are only 7 main classes of enzymes).[40] Another example is the conversion of a yeast galactokinase (Gal1) to a transcription factor (Gal3) which can be achieved by an insertion of only two amino acids.[41]

While some mutations may not change the molecular function of a protein significantly, their biological function may be dramatically changed. For instance, most brain receptors recognize specific neurotransmitters, but that specificity can easily be changed by mutations. This has been shown by acetylcholine receptors that can be changed to serotonin or glycine receptors which actually have very different functions. Their similar gene structure also indicates that they must have arisen from gene duplications.[42]

Protein structure. Although protein structures are highly conserved, sometimes one or a few mutations can dramatically change a protein. For instance, an IgG-binding, 4 +  fold can be transformed into an albumin-binding, 3-α fold via a single amino-acid mutation. This example also shows that such a transition can happen with neither function nor native structure being completely lost.[43] In other words, even when multiple mutations are required to convert one protein or structure into another, the structure and function is at least partially retained in the intermediary sequences. Similarly, domains can be converted into other domains (and thus other functions). For instance, the structures of SH3 folds can evolve into OB folds which in turn can evolve into CLB folds.[44]

Examples

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Evolutionary faunas

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A macroevolutionary benchmark study is Sepkoski's[45][46] work on marine animal diversity through the Phanerozoic. His iconic diagram of the numbers of marine families from the Cambrian to the Recent illustrates the successive expansion and dwindling of three "evolutionary faunas" that were characterized by differences in origination rates and carrying capacities. Long-term ecological changes and major geological events are postulated to have played crucial roles in shaping these evolutionary faunas.[47]

Stanley's rule

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Macroevolution is driven by differences between species in origination and extinction rates. Remarkably, these two factors are generally positively correlated: taxa that have typically high diversification rates also have high extinction rates. This observation has been described first by Steven Stanley, who attributed it to a variety of ecological factors.[48] Yet, a positive correlation of origination and extinction rates is also a prediction of the Red Queen hypothesis, which postulates that evolutionary progress (increase in fitness) of any given species causes a decrease in fitness of other species, ultimately driving to extinction those species that do not adapt rapidly enough.[49] High rates of origination must therefore correlate with high rates of extinction.[4] Stanley's rule, which applies to almost all taxa and geologic ages, is therefore an indication for a dominant role of biotic interactions in macroevolution.

"Macromutations": Single mutations leading to dramatic change

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Normal phenotype
 
Bithorax phenotype
Mutations in the Ultrabithorax gene lead to a duplication of wings in fruit flies.

While the vast majority of mutations are inconsequential, some can have a dramatic effect on morphology or other features of an organism. One of the best studied cases of a single mutation that leads to massive structural change is the Ultrabithorax mutation in fruit flies. The mutation duplicates the wings of a fly to make it look like a dragonfly, a different order of insect.

Evolution of multicellularity

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Main article: Multicellular organism

The evolution of multicellular organisms is one of the major breakthroughs in evolution. The first step of converting a unicellular organism into a metazoan (a multicellular organism) is to allow cells to attach to each other. This can be achieved by one or a few mutations. In fact, many bacteria form multicellular assemblies, e.g. cyanobacteria or myxobacteria. Another species of bacteria, Jeongeupia sacculi, form well-ordered sheets of cells, which ultimately develop into a bulbous structure.[50][51] Similarly, unicellular yeast cells can become multicellular by a single mutation in the ACE2 gene, which causes the cells to form a branched multicellular form.[52]

Evolution of bat wings

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The wings of bats have the same structural elements (bones) as any other five-fingered mammal (see periodicity in limb development). However, the finger bones in bats are dramatically elongated, so the question is how these bones became so long. It has been shown that certain growth factors such as bone morphogenetic proteins (specifically Bmp2) is over expressed so that it stimulates an elongation of certain bones. Genetic changes in the bat genome identified the changes that lead to this phenotype and it has been recapitulated in mice: when specific bat DNA is inserted in the mouse genome, recapitulating these mutations, the bones of mice grow longer.[53]

Limb loss in lizards and snakes

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Main article: Limbless vertebrates
 
Limbloss in lizards can be observed in the genus Lerista which shows many intermediary steps with increasing loss of digits and toes. The species shown here, Lerista cinerea, has no digits and only 1 toe left.

Snakes evolved from lizards. Phylogenetic analysis shows that snakes are actually nested within the phylogenetic tree of lizards, demonstrating that they have a common ancestor.[54] This split happened about 180 million years ago and several intermediary fossils are known to document the origin. In fact, limbs have been lost in numerous clades of reptiles, and there are cases of recent limb loss. For instance, the skink genus Lerista has lost limbs in multiple cases, with all possible intermediary steps, that is, there are species which have fully developed limbs, shorter limbs with 5, 4, 3, 2, 1 or no toes at all.[55]

Human evolution

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While human evolution from their primate ancestors did not require massive morphological changes, our brain has sufficiently changed to allow human consciousness and intelligence. While the latter involves relatively minor morphological changes it did result in dramatic changes to brain function.[56] Thus, macroevolution does not have to be morphological, it can also be functional.

Evolution of viviparity in lizards

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The European Common Lizard (Zootoca vivipara) consists of populations that are egg-laying or live-bearing, demonstrating that this dramatic difference can even evolve within a species.

Most lizards are egg-laying and thus need an environment that is warm enough to incubate their eggs. However, some species have evolved viviparity, that is, they give birth to live young, as almost all mammals do. In several clades of lizards, egg-laying (oviparous) species have evolved into live-bearing ones, apparently with very little genetic change. For instance, a European common lizard, Zootoca vivipara, is viviparous throughout most of its range, but oviparous in the extreme southwest portion.[57][58] That is, within a single species, a radical change in reproductive behavior has happened. Similar cases are known from South American lizards of the genus Liolaemus which have egg-laying species at lower altitudes, but closely related viviparous species at higher altitudes, suggesting that the switch from oviparous to viviparous reproduction does not require many genetic changes.[59]

Behavior: Activity pattern in mice

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Most animals are either active at night or during the day. However, some species switched their activity pattern from day to night or vice versa. For instance, the African striped mouse (Rhabdomys pumilio), transitioned from the ancestrally nocturnal behavior of its close relatives to a diurnal one. Genome sequencing and transcriptomics revealed that this transition was achieved by modifying genes in the rod phototransduction pathway, among others.[60]

Research topics

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Subjects studied within macroevolution include:[61]

See also

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Notes

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  1. ^ Rolland et al. (2023)[5] in the introduction describe ‘microevolution’ and ‘macroevolution’ occurring at two different scales; below the species level and at/above the species level respectively: “Since the modern synthesis, many evolutionary biologists have focused their attention on evolution at one of two different timescales: microevolution, that is, the evolution of populations below the species level (in fields such as population genetics, phylogeography and quantitative genetics), or macroevolution, that is, the evolution of species or higher taxonomic levels (for example, phylogenetics, palaeobiology and biogeography).”
  2. ^ Saupe & Myers (2021)[1] states: “Macroevolution is the study of patterns and processes associated with evolutionary change at and above the species level, and includes investigations of both evolutionary tempo and mode.”
  3. ^ Michael Hautmann (2019)[4] discusses 3 categories of definitions that have been historically used. He argues in favor of the following definition [added clarity]: "Macroevolution is evolutionary change that is guided by sorting of interspecific [between-species] variation."
  4. ^ David Jablonski (2017)[6][7] states: “Macroevolution, defined broadly as evolution above the species level, is thriving as a field.”
  5. ^ In his book “The Structure of Evolutionary Theory” (2002)[3] page 612, Stephen J. Gould describes the species as the basic unit of macroevolution, and compares speciation and extinction to birth and death in microevolutionary processes respectively: “In particular, and continuing to use species as a “type” example of individuality at higher levels, all evolutionary criteria apply to the species as a basic unit of macro-evolution. Species have children by branching (in our professional jargon, we even engender these offspring as “daughter species”). Speciation surely obeys principles of hereditary, for daughters, by strong constraints of homology, originate with phenotypes and genotypes closer to those of their parent than to any other species of a collateral lineage. Species certainly vary, for the defining property of reproductive isolation demands genetic differentiation from parents and collateral relatives. Finally, species interact with the environment in a causal way that can influence rates of birth (speciation) and death (extinction).”
  6. ^ In his paper proposing the theory of species selection, Steven M. Stanly (1974)[2] described macroevolution as being evolution above the species level and decoupled from microevolution: “In reaction to the arguments of macromutationists who opposed Neo-Darwinism, modern evolutionists have forcefully asserted that the process of natural selection is responsible for both microevolution, or evolution within species, and evolution above the species level, which is also known as macroevolution or transpecific evolution. [...] Macroevolution is decoupled from microevolution, and we must envision the process governing its course as being analogous to natural selection but operating at a higher level of biological organization. In this higher-level process species become analogous to individuals, and speciation replaces reproduction”
  7. ^ The ‘Understanding Evolution’ website[8] by UCMP: “Microevolution happens on a small scale (within a single population), while macroevolution happens on a scale that transcends the boundaries of a single species”
  8. ^ Thomas Holtz’s course GEOL331 lecture notes[9] discusses macroevolution observed in the fossil record:“Following these early attempted modifications of Darwinism, the rest of the 20th Century onward stayed largely within a Darwinian model. However, there were different major schools of thought. Many of these differences hinged on views of microevolution (evolutionary change within a species) and macroevolution (evolutionary change above the species level). While most agreed that the ultimate processes in macroevolution were ultimately microevolutionary, there were disagreement[s] whether the patterns produced were actually reducible to microevolutionary changes.”
  9. ^ The ‘Digital Atlas of Ancient Life’ website[10] by PRI provides a very detailed historical overview for the definition of ‘macroevolution’: “The meaning of the term “macroevolution” has shifted over time. Indeed, early definitions do to not necessarily make much sense in light of our current understanding of evolution, yet are still worth considering to show how the field itself has evolved. Here we will consider usage of the term macroevolution in a few key works, as well as present a definition of macroevolution that we endorse. [...] Lieberman and Eldredge (2014) defined macroevolution as “the patterns and processes pertaining to the birth, death, and persistence of species” and we adopt this definition here.”
  10. ^ a b c d The terms ('biotypes', 'Jordanone', and 'Linneone') used here by Filipchenko were/are rarely used among non-Russian speaking scientists. According to Krasil'nikov (1958),[14] these terms were used to describe the variety of forms observed within a single species: "With the development of genetics the concept of species widened according to the ideas of variability and heredity of organisms. New terms were introduced for the determination of species subdivision, such as "biotype", "pure line", "jardanon", "linneon", etc. ["Jardanon"--a simple means of classification of lower organisms. "Linneon"--the complex of "jardanons"--according to the Russian concept, the inner species variety of forms does not exceed the limits of qualitative unity of the species.]"


References

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  2. ^ a b c d e Stanley, S. M. (1 February 1975). "A theory of evolution above the species level". Proceedings of the National Academy of Sciences. 72 (2): 646–50. Bibcode:1975PNAS...72..646S. doi:10.1073/pnas.72.2.646. ISSN 0027-8424. PMC 432371. PMID 1054846.
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  4. ^ a b c d e f Hautmann, Michael (2020). "What is macroevolution?". Palaeontology. 63 (1): 1–11. Bibcode:2020Palgy..63....1H. doi:10.1111/pala.12465. ISSN 0031-0239.
  5. ^ a b c d Rolland, J.; Henao-Diaz, L.F.; Doebeli, M.; et al. (10 July 2023). "Conceptual and empirical bridges between micro- and macroevolution" (PDF). Nature Ecology & Evolution. 7 (8): 1181–1193. Bibcode:2023NatEE...7.1181R. doi:10.1038/s41559-023-02116-7. ISSN 2397-334X.
  6. ^ Jablonski, D. (3 June 2017). "Approaches to Macroevolution: 1. General Concepts and Origin of Variation". Springer, Evolutionary Biology. 44 (4): 427–450. Bibcode:2017EvBio..44..427J. doi:10.1007/s11692-017-9420-0. PMC 5661017. PMID 29142333.
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  14. ^ Krasilʹnikov, Nikolaĭ Aleksandrovich (1958). Soil microorganisms and higher plants (PDF). Moscow: Academy of Sciences of the USSR.
  15. ^ Hendricks, Jonathan R.; Saupe, Erin E; Myers, Corinne E.; Hermsen, Elizabeth J.; Allmon, Warren D. (2014). "he generification of the fossil record". Paleobiology. 40 (4): 511–528. doi:10.1666/13076.
  16. ^ a b Adams, Mark B (1990). "Filipchenko [Philiptschenko], Iurii Aleksandrovich". Dictionary of Scientific Biography. 17 (297–303).
  17. ^ Goldschmidt, R. (1933). "Some aspects of evolution". Science. 78 (2033): 539–547. Bibcode:1933Sci....78..539G. doi:10.1126/science.78.2033.539. PMID 17811930.
  18. ^ Goldschmidt, R. (1940). The material basis of evolution. Yale University Press.
  19. ^ Theißen, Günter (March 2009). "Saltational evolution: hopeful monsters are here to stay". Theory in Biosciences. 128 (1): 43–51. doi:10.1007/s12064-009-0058-z. ISSN 1431-7613. PMID 19224263. S2CID 4983539.
  20. ^ Rieppel, Olivier (13 March 2017). Turtles as hopeful monsters : origins and evolution. Bloomington, Indiana. ISBN 978-0-253-02507-4. OCLC 962141060.{{cite book}}: CS1 maint: location missing publisher (link)
  21. ^ Dobzhanski, T. (1937). Genetics and the origin of species. Columbia University Press.
  22. ^ Dawkins, Richard, 1941- (1982). The extended phenotype : the gene as the unit of selection. Oxford [Oxfordshire]: Freeman. ISBN 0-7167-1358-6. OCLC 7652745.{{cite book}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link)
  23. ^ Ayala Francisco J (1983). "Beyond Darwinism? The Challenge of Macroevolution to the Synthetic Theory of Evolution". In Asquith, Peter D and Nickles, Thomas (eds.). PSA 1982. Vol. 2. Philosophy of Science Association. pp. 118–132.
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