Parallel evolution

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Parallel evolution is the similar development of a trait in distinct species that are not closely related, but share a similar original trait in response to similar evolutionary pressure. [1] [2]

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Parallel vs. convergent evolution

Evolution at an amino acid position. In each case, the left-hand species changes from incorporating alanine (A) at a specific position within a protein in a hypothetical common ancestor deduced from comparison of sequences of several species, and now incorporates serine (S) in its present-day form. The right-hand species may undergo divergent evolution (alanine replaced with threonine instead), parallel evolution (alanine also replaced with serine), or convergent evolution (threonine replaced with serine) at this amino acid position relative to that of the first species. Evolutionary trends.svg
Evolution at an amino acid position. In each case, the left-hand species changes from incorporating alanine (A) at a specific position within a protein in a hypothetical common ancestor deduced from comparison of sequences of several species, and now incorporates serine (S) in its present-day form. The right-hand species may undergo divergent evolution (alanine replaced with threonine instead), parallel evolution (alanine also replaced with serine), or convergent evolution (threonine replaced with serine) at this amino acid position relative to that of the first species.

Given a trait that occurs in each of two lineages descended from a specified ancestor, it is possible in theory to define parallel and convergent evolutionary trends strictly, and distinguish them clearly from one another. [2] However the criteria for defining convergent as opposed to parallel evolution are unclear in practice, so that arbitrary diagnosis is common. When two species share a trait, evolution is defined as parallel if the ancestors are known to have shared that similarity; if not, it is defined as convergent. However, the stated conditions are a matter of degree; all organisms share common ancestors. Scientists differ on whether the distinction is useful. [3] [4]

Parallel evolution between marsupials and placentals

A number of examples of parallel evolution are provided by the two main branches of the mammals, the placentals and marsupials, which have followed independent evolutionary pathways following the break-up of land-masses such as Gondwanaland roughly 100 million years ago. In South America, marsupials and placentals shared the ecosystem (before the Great American Interchange); in Australia, marsupials prevailed; and in the Old World and North America the placentals won out. However, in all these localities mammals were small and filled only limited places in the ecosystem until the mass extinction of dinosaurs sixty-five million years ago. At this time, mammals on all three landmasses began to take on a much wider variety of forms and roles. While some forms were unique to each environment, surprisingly similar animals have often emerged in two or three of the separated continents. Examples of these include the placental sabre-toothed cats (Machairodontinae) and the South American marsupial sabre-tooth (Thylacosmilus); the Tasmanian wolf and the European wolf; likewise marsupial and placental moles, flying squirrels, and (arguably) mice.[ citation needed ]

Parallel coevolution of traits between hummingbirds and sunbirds contributing to ecological guilds

Hummingbirds and sunbirds, two nectarivorous bird lineages in the New and Old Worlds have parallelly evolved a suite of specialized behavioral and anatomical traits. These traits (bill shape, digestive enzymes, and flight) allow the birds to optimally fit the flower-feeding-and-pollination ecological niche they occupy, which is shaped by the birds' suites of parallel traits. Thus, a parallel coevolved behavioral syndrome within the birds creates an emergent guild of highly specialized birds and highly adapted plants, each exploiting the other's involvement in the flowers' pollination in the Old World and New World alike. [5]

The bill shape of nectarivores, being long and needle-like, allows them to reach down a flower's pistil/stamen and get at the nectar within. Nectarivores may also use their specialized bills to engage in nectar robbing, a practice seen in both hummingbirds and sunbirds in which the bird gets nectar by making a hole in the base of the flower's corolla tube instead of inserting its bill through the tube as is standard, thus "robbing" the flower of nectar since it is not pollinated it in return. [6]

Nectarivores and ornithophilous flowers often exist in mutualistic guild relationships facilitated by the bird's bill shape, food source, and digestive ability acting in concert with the flower's tube shape and adaptation to pollination by hovering or perching birds. The birds eat nectar using their long, thin bills and, in so doing, collect pollen on their bills; this pollen is then transferred to the next flower they feed on. This mutualism coevolved in parallel between the Old World and New World birds and their respective flowers. [7] Moreover, the digestive enzyme activity in nectarivores matching the nectar composition in their respective flowers appears to have coevolved in parallel between plants and pollinators across continents, as the nectarivorous lineages independently evolved the ability to digest the nectar specific to their flowers, resulting in distinct guilds. [7] [8]

The capacity of nectarivores to digest sucrose is far greater than that of other avian taxa. This difference is due to an analogous high concentration of sucrase-isomaltase, an enzyme that hydrolyzes sucrose. Sucrase activity per unit intestinal surface area appears to be higher in nectarivores than in other birds, meaning these nectarivorous avians can digest more sucrose more rapidly than other taxa. [8] Moreover, the Adaptive Modulation Hypothesis does not apply for nectarivores and sugar-digesting enzymes, meaning that two lineages of nectarivores should not necessarily both have high sucrase-isomaltase concentrations even though they both eat nectar. Thus, parallel acquisition of analogous sucrose digestive capability is a reasonable conclusion because there is no apparent cause for the two lineages to share this high enzyme concentration. [9]

Related Research Articles

<span class="mw-page-title-main">Hummingbird</span> Family of birds

Hummingbirds are birds native to the Americas and comprise the biological family Trochilidae. With about 366 species and 113 genera, they occur from Alaska to Tierra del Fuego, but most species are found in Central and South America. About 28 hummingbird species are listed as endangered or critically endangered, with numerous species declining in population.

<span class="mw-page-title-main">Convergent evolution</span> Independent evolution of similar features

Convergent evolution is the independent evolution of similar features in species of different periods or epochs in time. Convergent evolution creates analogous structures that have similar form or function but were not present in the last common ancestor of those groups. The cladistic term for the same phenomenon is homoplasy. The recurrent evolution of flight is a classic example, as flying insects, birds, pterosaurs, and bats have independently evolved the useful capacity of flight. Functionally similar features that have arisen through convergent evolution are analogous, whereas homologous structures or traits have a common origin but can have dissimilar functions. Bird, bat, and pterosaur wings are analogous structures, but their forelimbs are homologous, sharing an ancestral state despite serving different functions.

<span class="mw-page-title-main">Honey possum</span> Species of marsupial

The honey possum or noolbenger, is a tiny species of marsupial that feeds on the nectar and pollen of a diverse range of flowering plants. Found only in southwest Australia, it is an important pollinator for such plants as Banksia attenuata, Banksia coccinea and Adenanthos cuneatus.

<span class="mw-page-title-main">Coevolution</span> Two or more species influencing each others evolution

In biology, coevolution occurs when two or more species reciprocally affect each other's evolution through the process of natural selection. The term sometimes is used for two traits in the same species affecting each other's evolution, as well as gene-culture coevolution.

<span class="mw-page-title-main">Honeyeater</span> Family of birds

The honeyeaters are a large and diverse family, Meliphagidae, of small to medium-sized birds. The family includes the Australian chats, myzomelas, friarbirds, wattlebirds, miners and melidectes. They are most common in Australia and New Guinea, and found also in New Zealand, the Pacific islands as far east as Samoa and Tonga, and the islands to the north and west of New Guinea known as Wallacea. Bali, on the other side of the Wallace Line, has a single species.

<span class="mw-page-title-main">Sunbird</span> Family of birds

Sunbirds and spiderhunters make up the family Nectariniidae of passerine birds. They are small, slender passerines from the Old World, usually with downward-curved bills. Many are brightly coloured, often with iridescent feathers, particularly in the males. Many species also have especially long tail feathers. Their range extends through most of Africa to the Middle East, South Asia, South-east Asia and southern China, to Indonesia, New Guinea and northern Australia. Species diversity is highest in equatorial regions.

<i>Heliconia</i> Genus of plants

Heliconia is a genus of flowering plants in the monotypic family Heliconiaceae. Most of the ca 194 known species are native to the tropical Americas, but a few are indigenous to certain islands of the western Pacific and Maluku in Indonesia. Many species of Heliconia are found in the tropical forests of these regions. Most species are listed as either vulnerable or data deficient by the IUCN Red List of threatened species. Several species are widely cultivated as ornamentals, and a few are naturalized in Florida, Gambia, and Thailand.

<span class="mw-page-title-main">Giant hummingbird</span> Species of bird

The giant hummingbird is the only member of the genus Patagona and the largest member of the hummingbird family, weighing 18–24 g (0.63–0.85 oz) and having a wingspan of approximately 21.5 cm (8.5 in) and length of 23 cm (9.1 in). This is approximately the same length as a European starling or a northern cardinal, though the giant hummingbird is considerably lighter because it has a slender build and long bill, making the body a smaller proportion of the total length. This weight is almost twice that of the next heaviest hummingbird species and ten times that of the smallest, the bee hummingbird.

<i>Babiana ringens</i> Species of flowering plant

Babiana ringens, the rat's tail, is a flowering plant endemic to Cape Province of South Africa. The foliage is long and erect with an inflorescence consisting of a sterile main stalk adapted for ornithophily, pollination by birds. The plant bears bright red, tubular flowers on side branches close to the ground. It is a perennial that grows in nutrient-poor sandy soil and flowers during the winter rains.

<span class="mw-page-title-main">Zoophily</span> Pollination by animals

Zoophily, or zoogamy, is a form of pollination whereby pollen is transferred by animals, usually by invertebrates but in some cases vertebrates, particularly birds and bats, but also by other animals. Zoophilous species frequently have evolved mechanisms to make themselves more appealing to the particular type of pollinator, e.g. brightly colored or scented flowers, nectar, and appealing shapes and patterns. These plant-animal relationships are often mutually beneficial because of the food source provided in exchange for pollination.

<span class="mw-page-title-main">Nectar</span> Sugar-rich liquid produced by many flowering plants, that attracts pollinators and insects

Nectar is a sugar-rich liquid produced by plants in glands called nectaries or nectarines, either within the flowers with which it attracts pollinating animals, or by extrafloral nectaries, which provide a nutrient source to animal mutualists, which in turn provide herbivore protection. Common nectar-consuming pollinators include mosquitoes, hoverflies, wasps, bees, butterflies and moths, hummingbirds, honeyeaters and bats. Nectar plays a crucial role in the foraging economics and evolution of nectar-eating species; for example, nectar foraging behavior is largely responsible for the divergent evolution of the African honey bee, A. m. scutellata and the western honey bee.

<span class="mw-page-title-main">Nectarivore</span> Animal in which nectar is a main source of nutrition in their diet.

In zoology, a nectarivore is an animal which derives its energy and nutrient requirements from a diet consisting mainly or exclusively of the sugar-rich nectar produced by flowering plants.

<span class="mw-page-title-main">Ornithophily</span> Pollination by birds

Ornithophily or bird pollination is the pollination of flowering plants by birds. This sometimes coevolutionary association is derived from insect pollination (entomophily) and is particularly well developed in some parts of the world, especially in the tropics, Southern Africa, and on some island chains. The association involves several distinctive plant adaptations forming a "pollination syndrome". The plants typically have colourful, often red, flowers with long tubular structures holding ample nectar and orientations of the stamen and stigma that ensure contact with the pollinator. Birds involved in ornithophily tend to be specialist nectarivores with brushy tongues and long bills, that are either capable of hovering flight or light enough to perch on the flower structures.

<span class="mw-page-title-main">Pollination syndrome</span> Flower traits that attract pollinators

Pollination syndromes are suites of flower traits that have evolved in response to natural selection imposed by different pollen vectors, which can be abiotic or biotic, such as birds, bees, flies, and so forth through a process called pollinator-mediated selection. These traits include flower shape, size, colour, odour, reward type and amount, nectar composition, timing of flowering, etc. For example, tubular red flowers with copious nectar often attract birds; foul smelling flowers attract carrion flies or beetles, etc.

<span class="mw-page-title-main">Malachite sunbird</span> Species of bird

The malachite sunbird is a small nectarivorous bird found from the highlands of Ethiopia southwards to South Africa. They pollinate many flowering plants, particularly those with long corolla tubes, in the Fynbos.

<span class="mw-page-title-main">Gurney's sugarbird</span> Species of bird

Gurney's sugarbird is a medium-sized passerine endemic to the mid- and high-altitude grassland velds in southern Africa. It belongs to the family Promeropidae, which contains one genus, Promerops, and two species. Gurney's sugarbird feeds on nectar from Protea bushes as well as on small insects. This bird is characterized by its long, graduated tail and decurved beak.

<span class="mw-page-title-main">Nectar robbing</span> Foraging behavior

Nectar robbing is a foraging behavior utilized by some organisms that feed on floral nectar, carried out by feeding from holes bitten in flowers, rather than by entering through the flowers' natural openings. "Nectar robbers" usually feed in this way, avoiding contact with the floral reproductive structures, and therefore do not facilitate plant reproduction via pollination. Because many species that act as pollinators also act as nectar robbers, nectar robbing is considered to be a form of exploitation of plant-pollinator mutualism. While there is variation in the dependency on nectar for robber species, most species rob facultatively.

Eurotrochilus is an extinct genus of stem group hummingbirds (Trochilidae) and are the closest known relatives of the crown group Trochilidae. Despite Eurotrochilus being morphologically very similar to modern hummingbirds, they still retained several primitive features and are not closely related to any specific extant hummingbird in the crown group. There are currently two described species of Eurotrochilus: E. inexpectatus and E. noniewiczi.

References

  1. Parallel evolution, an example may be the Pyrotherians evolved a body plan similar to proboscideans: Online Biology Glossary Archived 2007-07-13 at the Wayback Machine
  2. 1 2 Zhang, J. and Kumar, S. 1997. Detection of convergent and parallel evolution at the amino acid sequence level Archived 2016-03-03 at the Wayback Machine . Mol. Biol. Evol.14, 527-36.
  3. Arendt, J.; REZNICK, D. (January 2008). "Convergence and parallelism reconsidered: what have we learned about the genetics of adaptation?". Trends in Ecology & Evolution. 23 (1): 26–32. doi:10.1016/j.tree.2007.09.011. PMID   18022278.
  4. Pearce, T. (10 November 2011). "Convergence and Parallelism in Evolution: A Neo-Gouldian Account". The British Journal for the Philosophy of Science. 63 (2): 429–448. doi:10.1093/bjps/axr046.
  5. Janeček, Štěpán; Chmel, Kryštof; Uceda Gómez, Guillermo; Janečková, Petra; Chmelová, Eliška; Sejfová, Zuzana; Luma Ewome, Francis (February 2020). "Ecological fitting is a sufficient driver of tight interactions between sunbirds and ornithophilous plants". Ecology and Evolution. 10 (4): 1784–1793. doi:10.1002/ece3.5942. ISSN   2045-7758. PMC   7042734 . PMID   32128116.
  6. Juan Francisco Ornelas. Serrate Tomia: An Adaptation for Nectar Robbing in Hummingbirds?. The Auk, Volume 111, Issue 3, Januar 1994, Pages 703710.
  7. 1 2 Janeček, Štěpán; Bartoš, Michael; Njabo, Kevin Yana (2015-01-22). "Convergent evolution of sunbird pollination systems of Impatiens species in tropical Africa and hummingbird systems of the New World". Biological Journal of the Linnean Society. 115 (1): 127–133. doi: 10.1111/bij.12475 . ISSN   0024-4066.
  8. 1 2 McWhorter, Todd J.; Rader, Jonathan A.; Schondube, Jorge E.; Nicolson, Susan W.; Pinshow, Berry; Fleming, Patricia A.; Gutiérrez-Guerrero, Yocelyn T.; Martínez del Rio, Carlos (July 2021). "Sucrose digestion capacity in birds shows convergent coevolution with nectar composition across continents". iScience. 24 (7): 102717. doi:10.1016/j.isci.2021.102717. ISSN   2589-0042. PMC   8246590 . PMID   34235412.
  9. Karasov, W. H. (1992-09-01). "Tests of the adaptive modulation hypothesis for dietary control of intestinal nutrient transport". American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 263 (3): R496–R502. doi:10.1152/ajpregu.1992.263.3.R496. ISSN   0363-6119.
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