Macroevolution

"Species selection operates on variation provided by the largely random process of speciation and favors species that speciate at high rates or survive for long periods and therefore tend to leave many daughter species."[1] Species selection comprises (a) effect-macroevolution, where organism-level traits (aggregate traits) affect speciation and extinction rates (Stanley's original concept), and (b) strict-sense species selection, where species-level traits (e.g. geographical range) affect speciation and extinction rates.[13] It has been argued that effect macroevolution is reducible to microevolution because both operate through selection on organismic traits,[14] but Grantham[15] demonstrated that effect macroevolution can oppose selection at the organismic level and is therefore not reducible microevolution. Cases in which selection on the same trait has opposing effects at the organismic and the species level have been made in the context of sexual selection,[16][17][18] which increases individual fitness but may also increase the extinction risk of the species.

One of the main questions in evolutionary biology is how fundamentally new structures evolve, such as new organs. As can be seen in vertebrate evolution, most "new" organs are actually not new—they are still modifications of previously existing organs. Examples are wings (modified limbs), feathers (modified reptile scales),[19] lungs (modified swim bladders, e.g. found in fish),[20][21] or even the heart (a muscularized segment of a vein).[22]

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.[23]

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.[24] 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.[25]

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.[26]

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${\displaystyle \beta }$+${\displaystyle \alpha }$ 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.[27] 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.

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 have also high extinction rates. This observation has been described first by Steven Stanley, who attributed it to a variety of ecological factors.[28] 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.[29] High rates of origination must therefore correlate with high rates of extinction.[3] Stanley's rule, which applies to almost all taxa and geologic ages, is therefore a strong indication for a dominant role of biotic interactions in macroevolution.

Mutations in the Ultrabithorax gene lead to a duplication of wings in 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 which represents a different order of insect.

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.[30][31] 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.[32]

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.[33]

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.[34] 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.[35]

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.[36] Thus, macroevolution does not have to be morphological, it can also be functional.

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 vivparous throughout most of its range, but oviparous in the extreme southwest portion.[37][38] 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.[39]