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Neoteny

Neoteny (/niˈɒtəni/),[1][2][3][4] also called juvenilization,[5] is the delaying or slowing of the physiological, or somatic, development of an organism, typically an animal. Neoteny is found in modern humans compared to other primates.[6] In progenesis or paedogenesis, sexual development is accelerated.[7]

Both neoteny and progenesis result in paedomorphism[8] (as having the form typical of children) or paedomorphosis[9] (changing towards forms typical of children), a type of heterochrony.[10] It is the retention in adults of traits previously seen only in the young. Such retention is important in evolutionary biology, domestication and evolutionary developmental biology. Some authors define paedomorphism as the retention of larval traits, as seen in salamanders.[11][12][13]

History and etymology edit

 
Diagram of the six types of shift in heterochrony, a change in the timing or rate of any process in embryonic development. Predisplacement, hypermorphosis, and acceleration (red) extend development (peramorphosis); postdisplacement, hypomorphosis, and deceleration (blue) all truncate it (paedomorphosis).

The origins of the concept of neoteny have been traced to biblical times[vague] (as argued by Ashley Montagu)[14] and to the poet William Wordsworth's "The Child is the father of the Man" (as argued by Barry Bogin).[15] The term itself was invented in 1885 by Julius Kollmann as he described the axolotl's maturation while remaining in a tadpole-like aquatic stage complete with gills, unlike other adult amphibians like frogs and toads.[16][17]

The word neoteny is borrowed from the German Neotenie, the latter constructed by Kollmann from the Greek νέος (neos, "young") and τείνειν (teínein, "to stretch, to extend"). The adjective is either "neotenic" or "neotenous".[18] For the opposite of "neotenic", different authorities use either "gerontomorphic"[19][20] or "peramorphic".[21] Bogin points out that Kollmann had intended the meaning to be "retaining youth", but had evidently confused the Greek teínein with the Latin tenere, which had the meaning he wanted, "to retain", so that the new word would mean "the retaining of youth (into adulthood)".[17]

In 1926, Louis Bolk described neoteny as the major process in humanization.[22][17] In his 1977 book Ontogeny and Phylogeny,[23] Stephen Jay Gould noted that Bolk's account constituted an attempted justification for "scientific" racism and sexism, but acknowledged that Bolk had been right in the core idea that humans differ from other primates in becoming sexually mature in an infantile stage of body development.[17]

In humans edit

Neoteny in humans is the slowing or delaying of body development, compared to non-human primates, resulting in features such as a large head, a flat face, and relatively short arms. These neotenic changes may have been brought about by sexual selection in human evolution. In turn, they may have permitted the development of human capacities such as emotional communication. However, humans also have relatively large noses and long legs, both peramorphic (not neotenic) traits. Some evolutionary theorists have proposed that neoteny was a key feature in human evolution.[24] J. B. S. Haldane states a "major evolutionary trend in human beings" is "greater prolongation of childhood and retardation of maturity."[5] Delbert D. Thiessen said that "neoteny becomes more apparent as early primates evolved into later forms" and that primates have been "evolving toward flat face."[25] Doug Jones argued that human evolution's trend toward neoteny may have been caused by sexual selection in human evolution for neotenous facial traits in women by men with the resulting neoteny in male faces being a "by-product" of sexual selection for neotenous female faces.[26]

In domestic animals edit

Neoteny is seen in domesticated animals such as dogs and mice.[27] This is because there are more resources available, less competition for those resources, and with the lowered competition the animals expend less energy obtaining those resources. This allows them to mature and reproduce more quickly than their wild counterparts.[27] The environment that domesticated animals are raised in determines whether or not neoteny is present in those animals. Evolutionary neoteny can arise in a species when those conditions occur, and a species becomes sexually mature ahead of its "normal development". Another explanation for the neoteny in domesticated animals can be the selection for certain behavioral characteristics. Behavior is linked to genetics which therefore means that when a behavioral trait is selected for, a physical trait may also be selected for due to mechanisms like linkage disequilibrium. Often, juvenile behaviors are selected for in order to more easily domesticate a species; aggressiveness in certain species comes with adulthood when there is a need to compete for resources. If there is no need for competition, then there is no need for aggression. Selecting for juvenile behavioral characteristics can lead to neoteny in physical characteristics because, for example, with the reduced need for behaviors like aggression, there is no need for developed traits that would help in that area. Traits that may become neotenized due to decreased aggression may be a shorter muzzle and smaller general size among the domesticated individuals. Some common neotenous physical traits in domesticated animals (mainly dogs, pigs, ferrets, cats, and even foxes) include floppy ears, changes in the reproductive cycle, curly tails, piebald coloration, fewer or shortened vertebra, large eyes, rounded forehead, large ears, and shortened muzzle.[28][29]

 
Neoteny and reduction in skull size – grey wolf and chihuahua skulls

When the role of dogs expanded from just being working dogs to also being companions, humans started selective breeding dogs for morphological neoteny, and this selective breeding for "neoteny or paedomorphism" "strengthened the human-canine bond."[30] Humans bred dogs to have more "juvenile physical traits" as adults, such as short snouts and wide-set eyes which are associated with puppies because people usually consider these traits to be more attractive. Some breeds of dogs with short snouts and broad heads such as the Komondor, Saint Bernard and Maremma Sheepdog are more morphologically neotenous than other breeds of dogs.[31] Cavalier King Charles spaniels are an example of selection for neoteny because they exhibit large eyes, pendant-shaped ears and compact feet, giving them a morphology similar to puppies as adults.[30]

In 2004, a study that used 310 wolf skulls and over 700 dog skulls representing 100 breeds concluded that the evolution of dog skulls can generally not be described by heterochronic processes such as neoteny, although some pedomorphic dog breeds have skulls that resemble the skulls of juvenile wolves.[32] By 2011, the findings by the same researcher were simply "Dogs are not paedomorphic wolves."[33]

In other species edit

 
The axolotl is a neotenous salamander, often retaining gills throughout its life.

Neoteny has been observed in many other species. It is important to note the difference between partial and full neoteny when looking at other species, to distinguish between juvenile traits which are advantageous in the short term and traits which are beneficial throughout the organism's life; this might provide insight into the cause of neoteny in a species. Partial neoteny is the retention of the larval form beyond the usual age of maturation, with possible sexual development (progenesis) and eventual maturation into the adult form; this is seen in the frog Lithobates clamitans. Full neoteny is seen in Ambystoma mexicanum and some populations of Ambystoma tigrinum, which remain in larval form throughout their lives.[34][35] Lithobates clamitans is partially neotenous; it delays maturation during the winter as fewer resources are available; it can find resources more easily in its larval form. This encompasses both of the main causes of neoteny; the energy required to survive in the winter as a newly-formed adult is too great, so the organism exhibits neotenous characteristics until it can better survive as an adult. Ambystoma tigrinum retains its neoteny for a similar reason; however, the retention is permanent due to the lack of available resources throughout its lifetime. This is another example of an environmental cause of neoteny. Several avian species, such as the manakins Chiroxiphia linearis and Chiroxiphia caudata, exhibit partial neoteny. The males of both species retain juvenile plumage into adulthood, losing it when they are fully mature.[36] In some bird species, the retention of juvenile plumage is linked to the molting time in each species. To ensure no overlap between molting and mating times, the birds may exhibit partial neoteny in plumage; males do not attain their bright, adult plumage before the females are prepared to mate. Neoteny is present because there is no need for the males to molt early, and trying to mate with immature females would be energy-inefficient.

Neoteny is commonly seen in flightless insects, such as the females of the order Strepsiptera. Flightlessness in insects has evolved separately a number of times; factors which may have contributed to the separate evolution of flightlessness are high altitude, geographic isolation (islands), and low temperatures.[37] Under these environmental conditions, dispersal would be disadvantageous; heat is lost more rapidly through wings in colder climates. The females of certain insect groups become sexually mature without metamorphosis, and some do not develop wings. Flightlessness in some female insects has been linked to higher fecundity.[37] Aphids are an example of insects which may never develop wings, depending on their environment. If resources are abundant on a host plant, there is no need to grow wings and disperse. If resources become diminished, their offspring may develop wings to disperse to other host plants.[38]

Two environments which favor neoteny are high altitudes and cool temperatures, because neotenous individuals have more fitness than individuals which metamorphose into an adult form. The energy required for metamorphosis detracts from individual fitness, and neotenous individuals can utilize available resources more easily.[39] This trend is seen in a comparison of salamander species at lower and higher altitudes; in a cool, high-altitude environment, neotenous individuals survive more and are more fecund than those which metamorphose into adult form.[39] Insects in cooler environments tend to exhibit neoteny in flight because wings have a high surface area and lose heat quickly; it is disadvantageous for insects to metamorphose into adults.[37]

Many species of salamander, and amphibians in general, exhibit environmental neoteny. Axolotl and olm are salamander species which retain their juvenile aquatic form throughout adulthood, examples of full neoteny. Gills are a common juvenile characteristic in amphibians which are kept after maturation; examples are the tiger salamander and rough-skinned newt, both of which retain gills into adulthood.[34]

Bonobos share many physical characteristics with humans, including neotenous skulls.[40] The shape of their skull does not change into adulthood (only increasing in size), due to sexual dimorphism and an evolutionary change in the timing of development.[40] Juveniles became sexually mature before their bodies had fully developed as adults and, due to a selective advantage, the skull's neotenic structure remained.[citation needed]

In some groups, such as the insect families Gerridae, Delphacidae and Carabidae, energy costs result in neoteny; many species in these families have small, neotenous wings or none at all.[38] Some cricket species shed their wings in adulthood;[41] in the genus Ozopemon, males (thought to be the first example of neoteny in beetles) are significantly smaller than females due to inbreeding.[42] In the termite Kalotermes flavicollis, neoteny is seen in molting females.[43]

In other species, such as the northwestern salamander (Ambystoma gracile), environmental conditions – high altitude, in this case – cause neoteny.[44] Neoteny is also found in a few species of the crustacean family Ischnomesidae, which live in deep ocean water.[45]

Subcellular neoteny edit

Neoteny is usually used to describe animal development; however, neoteny is also seen in the cell organelles. It was suggested that subcellular neoteny could explain why sperm cells have atypical centrioles. One of the two sperm centrioles of fruit fly exhibit the retention of “juvenile” centriole structure, which can be described as centriolar “neoteny”. This neotenic, atypical centriole is known as the Proximal Centriole-Like. Typical centrioles form via a step by step process in which a cartwheel forms, then develops to become a procentriole, and further matures into a centriole. The neotenic centriole of fruit fly resembles an early procentriole.[46]

See also edit

References edit

  1. ^ "neoteny". Dictionary.com Unabridged (Online). n.d. Retrieved April 21, 2019.
  2. ^ "neoteny". The American Heritage Dictionary of the English Language (5th ed.). HarperCollins. Retrieved April 21, 2019.
  3. ^ . Lexico US English Dictionary. Oxford University Press. Archived from the original on 2020-03-22.
  4. ^ "neoteny". Merriam-Webster.com Dictionary. Retrieved April 21, 2019.
  5. ^ a b Montagu, A. (1989). Growing Young. Bergin & Garvey: CT.
  6. ^ Choi, Charles Q. (1 July 2009). "Being More Infantile May Have Led to Bigger Brains". Scientific American.
  7. ^ Volkenstein, M. V. 1994. Physical Approaches to Biological Evolution. Springer-Verlag: Berlin, [1].
  8. ^ "Paedomorphic". 21 January 2022.
  9. ^ "Morphosis". 6 June 2022.
  10. ^ Ridley, Mark (1985). Evolution. Blackwell.
  11. ^ Whiteman, H.H. (1994). "Evolution of facultative paedomorphosis". Quarterly Review of Biology. 69 (2): 205–221. doi:10.1086/418540. S2CID 83500486.
  12. ^ Schell, S. C. Handbook of Trematodes of North America North of Mexico, 1985, pg. 22
  13. ^ Ginetsinskaya, T.A. Trematodes, Their Life Cycles, Biology and Evolution. Leningrad, USSR: Nauka 1968. Translated in 1988, [2].
  14. ^ Montagu, Ashley (1989). Growing Young. Bloomsbury Academic. ISBN 978-0-89789-167-7. Retrieved 17 January 2024.
  15. ^ Bogin, Barry (6 December 1998). "Evolutionary hypotheses for human childhood". Cover Image American Journal of Physical Anthropology. Wiley Periodicals LLC. 104 (S25): 66. doi:10.1002/(SICI)1096-8644(1997)25+%3C63::AID-AJPA3%3E3.0.CO;2-8. hdl:2027.42/37682. ISSN 0002-9483. Retrieved 17 January 2024. William Wordsworth, for example, praised the concept of neoteny in 1802 with words of innocence and hope
  16. ^ Kollmann, J. (1885). "Das Ueberwintern von europäischen Frosch- und Tritonlarven und die Umwandlung des mexikanischen Axolotl" [The overwintering of European frog- and triton larvae and the transformation of the Mexican axolotl]. Verhandlungen der Naturforschenden Gesellschaft in Basel (Proceedings of the Natural Science Society of Basel) (in German). 7: 387–398. From pp. 397–398: "Dann drängt sich die Frage auf, ob das Latenzstadium der Eier, das einerseits bei Fischen, Vögeln and Säugethieren in so höchst überraschenden Formen vorkommt, anderseits das Latenzstadium bei den Wirbellosen ¹) nicht eine Variante derselben Eigenschaft der Organismen sei, welche ich Neotenie genannt habe, und die auf irgend einer Entwichlungsstufe in Kraft treten kann." (Then the question arises whether on the one hand the latency stage of eggs — which occurs in such highly surprising forms in fish, birds and mammals — [and] on the other hand the latency stage in invertebrates ¹) be not a variant of the same property of the organisms, which I have called "neoteny" and which can come into force at any stage of development.)
  17. ^ a b c d Bogin, Barry (1999). Patterns of Human Growth. Cambridge University Press. pp. 157–169. ISBN 978-0-521-56438-0.
  18. ^ Neoteny, The Free Dictionary. 2011. Accessed April 30, 2011.
  19. ^ Henke, W. (2007). Handbook of paleoanthropology, Volume 1. Springer Books, NY.
  20. ^ Hetherington, R. (2010). The Climate Connection: Climate Change and Modern Human Evolution. Cambridge University Press.
  21. ^ Hall, B.K., Hallgrímsson, B. Monroe, W.S. (2008). Strickberger's evolution: the integration of genes, organisms and populations. Jones and Bartlett Publishers: Canada.
  22. ^ Bolk, Louis (1926). Das Problem der Menschwerdung : Vortrag gehalten am 15. April 1926 auf der XXV. Versammlung der anatomischen Gesellschaft zu Freiburg [The Problem of Humanization: Lecture held on 15 April 1926 at the 25th Congress of the Anatomical Society at Freiberg] (in German). Jena, Germany: Gustav Fischer.
  23. ^ Gould, Stephen Jay (1977). Ontogeny and Phylogeny. Cambridge, Massachusetts: Belknap (Harvard University Press). ISBN 978-0-674-63940-9.
  24. ^ Shea, Brian T. (1989). "Heterochrony in human evolution: The case for neoteny reconsidered". American Journal of Physical Anthropology. 32 (S10): 69–101. doi:10.1002/ajpa.1330320505.
  25. ^ Thiessen, D.D. (1997). Bittersweet destiny: the stormy evolution of human behavior. Transaction Publishers, N.J.
  26. ^ Jones, D.; et al. (1995). "Sexual selection, physical attractiveness, and facial neoteny: Cross-cultural evidence and implications [and comments and reply]". Current Anthropology. 36 (5): 723–748. doi:10.1086/204427. S2CID 52840802.
  27. ^ a b Price, E. (1999). "Behavioral development in animals undergoing domestication". Applied Animal Behaviour Science. 65 (3): 245–271. doi:10.1016/S0168-1591(99)00087-8.
  28. ^ Bertone, J. (2006). Equine geriatric medicine and surgery. Saunders, MI.
  29. ^ Trut, L. N. (1999). "Early canid domestication: the farm-fox experiment". American Scientist. 87 (2): 160–169. Bibcode:1999AmSci..87.....T. doi:10.1511/1999.2.160.
  30. ^ a b McGreevy, P.D. & Nicholas, F.W. (1999). Some Practical Solutions to Welfare Problems in Dog Breeding. In Animal Welfare. 8: 329–341.
  31. ^ Beck, A.M. & Katcher, A.H. (1996). Between Pets and People: The Importance of Companionship. West Lafayette, Indiana: Purdue University Press. ISBN 1-55753-077-7
  32. ^ Drake, Abby Grace, "Evolution and development of the skull morphology of canids: An investigation of morphological integration and heterochrony" (January 1, 2004). Doctoral Dissertations Available from Proquest. Paper AAI3136721. link
  33. ^ Drake, Abby Grace (2011). "Dispelling dog dogma: An investigation of heterochrony in dogs using 3D geometric morphometric analysis of skull shape". Evolution & Development. 13 (2): 204–213. doi:10.1111/j.1525-142X.2011.00470.x. PMID 21410876. S2CID 20893501.
  34. ^ a b Swingle, W. (1922). "Experiments on the metamorphosis of neotenous amphibians". Journal of Experimental Zoology. 36 (4): 397–421. doi:10.1002/jez.1400360402.
  35. ^ "Ambystoma tigrinum". Amphibia Web.
  36. ^ Foster, M. (1987). "Delayed maturation, neoteny, and social system differences in two manakins of genus Chiroxyphia". Evolution. 41 (3): 547–558. doi:10.2307/2409256. JSTOR 2409256. PMID 28563802.
  37. ^ a b c Barbosa, P.; et al. (1989). "Life-history traits of forest-inhabiting flightless Lepidoptera". American Midland Naturalist. 122 (2): 262–274. doi:10.2307/2425912. JSTOR 2425912.
  38. ^ a b Harrison, R (1980). "Dispersal polymorphisms in insects". Annual Review of Ecology and Systematics. 11: 95–118. doi:10.1146/annurev.es.11.110180.000523. JSTOR 2096904.
  39. ^ a b Snyder, R (1956). "Comparative Features of the Life Histories of Ambystoma gracile (Baird) from Populations at Low and High Altitudes". Copeia. 1956 (1): 41–50. doi:10.2307/1439242. JSTOR 1439242.
  40. ^ a b Shea, B. T. (1983). "Paedomorphosis and Neoteny in the Pygmy Chimpanzee". Science. 222 (4623): 521–522. Bibcode:1983Sci...222..521S. doi:10.1126/science.6623093. JSTOR 1691380. PMID 6623093.
  41. ^ Harrison, R (1980). "Dispersal Polymorphisms in Insects". Annual Review of Ecology and Systematics. 11: 95–118. doi:10.1146/annurev.es.11.110180.000523. JSTOR 2096904.
  42. ^ Jordal, B. H.; Beaver, R. A.; Normark, B. B.; Farrell, B. D. (2002). "Extraordinary sex ratios and the evolution of male neoteny in sib-mating Ozopemon beetles". Biological Journal of the Linnean Society. 75 (3): 353–360. doi:10.1046/j.1095-8312.2002.00025.x.
  43. ^ Soltani-Mazouni, N.; Bordereau, C. (1987). "Changes in the cuticle, ovaries and colleterial glands during the pseudergate and neotenic molt in Kalotermes flavicollis (FABR.) (Isoptera : Kalotermitidae)". International Journal of Insect Morphology and Embryology. 16 (3–4): 221–225. doi:10.1016/0020-7322(87)90022-5.
  44. ^ Eagleson, G.; McKeown, B. (1978). "Changes in thyroid activity of Ambystoma gracile (Baird) during different larval, transforming, and postmetamorphic phases". Canadian Journal of Zoology. 56 (6): 1377–1381. doi:10.1139/z78-190.
  45. ^ Brokeland, W.; Brandt, A. (2004). "Two new species of Ischnomesidae (Crustacea: Isopoda) from the Southern Ocean displaying neoteny". Deep-Sea Research Part II. 51 (14–16): 1769–1785. Bibcode:2004DSRII..51.1769B. doi:10.1016/j.dsr2.2004.06.034.
  46. ^ Avidor-Reiss, Tomer; Turner, Katerina (2019), Kloc, Malgorzata (ed.), "The Evolution of Centriole Structure: Heterochrony, Neoteny, and Hypermorphosis", The Golgi Apparatus and Centriole: Functions, Interactions and Role in Disease, Results and Problems in Cell Differentiation, Cham: Springer International Publishing, vol. 67, pp. 3–15, doi:10.1007/978-3-030-23173-6_1, ISBN 978-3-030-23173-6, PMC 7576685, PMID 31435789, retrieved 2023-10-12

Further reading edit

  • Bergstorm, Carl T. & Dugatkin, Lee Alan (2012). Evolution, W.W. Norton ISBN 039391349X

External links edit

  • Singer, Emily (2015-06-02). "How Dinosaurs Shrank and Became Birds". Quanta Magazine.

neoteny, paedogenesis, redirects, here, topic, soil, formation, pedogenesis, also, called, juvenilization, delaying, slowing, physiological, somatic, development, organism, typically, animal, found, modern, humans, compared, other, primates, progenesis, paedog. Paedogenesis redirects here For the topic of soil formation see Pedogenesis Neoteny n i ˈ ɒ t en i 1 2 3 4 also called juvenilization 5 is the delaying or slowing of the physiological or somatic development of an organism typically an animal Neoteny is found in modern humans compared to other primates 6 In progenesis or paedogenesis sexual development is accelerated 7 Both neoteny and progenesis result in paedomorphism 8 as having the form typical of children or paedomorphosis 9 changing towards forms typical of children a type of heterochrony 10 It is the retention in adults of traits previously seen only in the young Such retention is important in evolutionary biology domestication and evolutionary developmental biology Some authors define paedomorphism as the retention of larval traits as seen in salamanders 11 12 13 Contents 1 History and etymology 2 In humans 3 In domestic animals 4 In other species 5 Subcellular neoteny 6 See also 7 References 8 Further reading 9 External linksHistory and etymology edit nbsp Diagram of the six types of shift in heterochrony a change in the timing or rate of any process in embryonic development Predisplacement hypermorphosis and acceleration red extend development peramorphosis postdisplacement hypomorphosis and deceleration blue all truncate it paedomorphosis The origins of the concept of neoteny have been traced to biblical times vague as argued by Ashley Montagu 14 and to the poet William Wordsworth s The Child is the father of the Man as argued by Barry Bogin 15 The term itself was invented in 1885 by Julius Kollmann as he described the axolotl s maturation while remaining in a tadpole like aquatic stage complete with gills unlike other adult amphibians like frogs and toads 16 17 The word neoteny is borrowed from the German Neotenie the latter constructed by Kollmann from the Greek neos neos young and teinein teinein to stretch to extend The adjective is either neotenic or neotenous 18 For the opposite of neotenic different authorities use either gerontomorphic 19 20 or peramorphic 21 Bogin points out that Kollmann had intended the meaning to be retaining youth but had evidently confused the Greek teinein with the Latin tenere which had the meaning he wanted to retain so that the new word would mean the retaining of youth into adulthood 17 In 1926 Louis Bolk described neoteny as the major process in humanization 22 17 In his 1977 book Ontogeny and Phylogeny 23 Stephen Jay Gould noted that Bolk s account constituted an attempted justification for scientific racism and sexism but acknowledged that Bolk had been right in the core idea that humans differ from other primates in becoming sexually mature in an infantile stage of body development 17 In humans editMain article Neoteny in humans Neoteny in humans is the slowing or delaying of body development compared to non human primates resulting in features such as a large head a flat face and relatively short arms These neotenic changes may have been brought about by sexual selection in human evolution In turn they may have permitted the development of human capacities such as emotional communication However humans also have relatively large noses and long legs both peramorphic not neotenic traits Some evolutionary theorists have proposed that neoteny was a key feature in human evolution 24 J B S Haldane states a major evolutionary trend in human beings is greater prolongation of childhood and retardation of maturity 5 Delbert D Thiessen said that neoteny becomes more apparent as early primates evolved into later forms and that primates have been evolving toward flat face 25 Doug Jones argued that human evolution s trend toward neoteny may have been caused by sexual selection in human evolution for neotenous facial traits in women by men with the resulting neoteny in male faces being a by product of sexual selection for neotenous female faces 26 In domestic animals editFurther information Domestication of animals Neoteny is seen in domesticated animals such as dogs and mice 27 This is because there are more resources available less competition for those resources and with the lowered competition the animals expend less energy obtaining those resources This allows them to mature and reproduce more quickly than their wild counterparts 27 The environment that domesticated animals are raised in determines whether or not neoteny is present in those animals Evolutionary neoteny can arise in a species when those conditions occur and a species becomes sexually mature ahead of its normal development Another explanation for the neoteny in domesticated animals can be the selection for certain behavioral characteristics Behavior is linked to genetics which therefore means that when a behavioral trait is selected for a physical trait may also be selected for due to mechanisms like linkage disequilibrium Often juvenile behaviors are selected for in order to more easily domesticate a species aggressiveness in certain species comes with adulthood when there is a need to compete for resources If there is no need for competition then there is no need for aggression Selecting for juvenile behavioral characteristics can lead to neoteny in physical characteristics because for example with the reduced need for behaviors like aggression there is no need for developed traits that would help in that area Traits that may become neotenized due to decreased aggression may be a shorter muzzle and smaller general size among the domesticated individuals Some common neotenous physical traits in domesticated animals mainly dogs pigs ferrets cats and even foxes include floppy ears changes in the reproductive cycle curly tails piebald coloration fewer or shortened vertebra large eyes rounded forehead large ears and shortened muzzle 28 29 nbsp Neoteny and reduction in skull size grey wolf and chihuahua skullsWhen the role of dogs expanded from just being working dogs to also being companions humans started selective breeding dogs for morphological neoteny and this selective breeding for neoteny or paedomorphism strengthened the human canine bond 30 Humans bred dogs to have more juvenile physical traits as adults such as short snouts and wide set eyes which are associated with puppies because people usually consider these traits to be more attractive Some breeds of dogs with short snouts and broad heads such as the Komondor Saint Bernard and Maremma Sheepdog are more morphologically neotenous than other breeds of dogs 31 Cavalier King Charles spaniels are an example of selection for neoteny because they exhibit large eyes pendant shaped ears and compact feet giving them a morphology similar to puppies as adults 30 In 2004 a study that used 310 wolf skulls and over 700 dog skulls representing 100 breeds concluded that the evolution of dog skulls can generally not be described by heterochronic processes such as neoteny although some pedomorphic dog breeds have skulls that resemble the skulls of juvenile wolves 32 By 2011 the findings by the same researcher were simply Dogs are not paedomorphic wolves 33 In other species edit nbsp The axolotl is a neotenous salamander often retaining gills throughout its life Neoteny has been observed in many other species It is important to note the difference between partial and full neoteny when looking at other species to distinguish between juvenile traits which are advantageous in the short term and traits which are beneficial throughout the organism s life this might provide insight into the cause of neoteny in a species Partial neoteny is the retention of the larval form beyond the usual age of maturation with possible sexual development progenesis and eventual maturation into the adult form this is seen in the frog Lithobates clamitans Full neoteny is seen in Ambystoma mexicanum and some populations of Ambystoma tigrinum which remain in larval form throughout their lives 34 35 Lithobates clamitans is partially neotenous it delays maturation during the winter as fewer resources are available it can find resources more easily in its larval form This encompasses both of the main causes of neoteny the energy required to survive in the winter as a newly formed adult is too great so the organism exhibits neotenous characteristics until it can better survive as an adult Ambystoma tigrinum retains its neoteny for a similar reason however the retention is permanent due to the lack of available resources throughout its lifetime This is another example of an environmental cause of neoteny Several avian species such as the manakins Chiroxiphia linearis and Chiroxiphia caudata exhibit partial neoteny The males of both species retain juvenile plumage into adulthood losing it when they are fully mature 36 In some bird species the retention of juvenile plumage is linked to the molting time in each species To ensure no overlap between molting and mating times the birds may exhibit partial neoteny in plumage males do not attain their bright adult plumage before the females are prepared to mate Neoteny is present because there is no need for the males to molt early and trying to mate with immature females would be energy inefficient Neoteny is commonly seen in flightless insects such as the females of the order Strepsiptera Flightlessness in insects has evolved separately a number of times factors which may have contributed to the separate evolution of flightlessness are high altitude geographic isolation islands and low temperatures 37 Under these environmental conditions dispersal would be disadvantageous heat is lost more rapidly through wings in colder climates The females of certain insect groups become sexually mature without metamorphosis and some do not develop wings Flightlessness in some female insects has been linked to higher fecundity 37 Aphids are an example of insects which may never develop wings depending on their environment If resources are abundant on a host plant there is no need to grow wings and disperse If resources become diminished their offspring may develop wings to disperse to other host plants 38 Two environments which favor neoteny are high altitudes and cool temperatures because neotenous individuals have more fitness than individuals which metamorphose into an adult form The energy required for metamorphosis detracts from individual fitness and neotenous individuals can utilize available resources more easily 39 This trend is seen in a comparison of salamander species at lower and higher altitudes in a cool high altitude environment neotenous individuals survive more and are more fecund than those which metamorphose into adult form 39 Insects in cooler environments tend to exhibit neoteny in flight because wings have a high surface area and lose heat quickly it is disadvantageous for insects to metamorphose into adults 37 Many species of salamander and amphibians in general exhibit environmental neoteny Axolotl and olm are salamander species which retain their juvenile aquatic form throughout adulthood examples of full neoteny Gills are a common juvenile characteristic in amphibians which are kept after maturation examples are the tiger salamander and rough skinned newt both of which retain gills into adulthood 34 Bonobos share many physical characteristics with humans including neotenous skulls 40 The shape of their skull does not change into adulthood only increasing in size due to sexual dimorphism and an evolutionary change in the timing of development 40 Juveniles became sexually mature before their bodies had fully developed as adults and due to a selective advantage the skull s neotenic structure remained citation needed In some groups such as the insect families Gerridae Delphacidae and Carabidae energy costs result in neoteny many species in these families have small neotenous wings or none at all 38 Some cricket species shed their wings in adulthood 41 in the genus Ozopemon males thought to be the first example of neoteny in beetles are significantly smaller than females due to inbreeding 42 In the termite Kalotermes flavicollis neoteny is seen in molting females 43 In other species such as the northwestern salamander Ambystoma gracile environmental conditions high altitude in this case cause neoteny 44 Neoteny is also found in a few species of the crustacean family Ischnomesidae which live in deep ocean water 45 Subcellular neoteny editNeoteny is usually used to describe animal development however neoteny is also seen in the cell organelles It was suggested that subcellular neoteny could explain why sperm cells have atypical centrioles One of the two sperm centrioles of fruit fly exhibit the retention of juvenile centriole structure which can be described as centriolar neoteny This neotenic atypical centriole is known as the Proximal Centriole Like Typical centrioles form via a step by step process in which a cartwheel forms then develops to become a procentriole and further matures into a centriole The neotenic centriole of fruit fly resembles an early procentriole 46 See also editAgeing Cuteness Kawaii Larviform female Moe slang NeoteninReferences edit neoteny Dictionary com Unabridged Online n d Retrieved April 21 2019 neoteny The American Heritage Dictionary of the English Language 5th ed HarperCollins Retrieved April 21 2019 neoteny Lexico US English Dictionary Oxford University Press Archived from the original on 2020 03 22 neoteny Merriam Webster com Dictionary Retrieved April 21 2019 a b Montagu A 1989 Growing Young Bergin amp Garvey CT Choi Charles Q 1 July 2009 Being More Infantile May Have Led to Bigger Brains Scientific American Volkenstein M V 1994 Physical Approaches to Biological Evolution Springer Verlag Berlin 1 Paedomorphic 21 January 2022 Morphosis 6 June 2022 Ridley Mark 1985 Evolution Blackwell Whiteman H H 1994 Evolution of facultative paedomorphosis Quarterly Review of Biology 69 2 205 221 doi 10 1086 418540 S2CID 83500486 Schell S C Handbook of Trematodes of North America North of Mexico 1985 pg 22 Ginetsinskaya T A Trematodes Their Life Cycles Biology and Evolution Leningrad USSR Nauka 1968 Translated in 1988 2 Montagu Ashley 1989 Growing Young Bloomsbury Academic ISBN 978 0 89789 167 7 Retrieved 17 January 2024 Bogin Barry 6 December 1998 Evolutionary hypotheses for human childhood Cover Image American Journal of Physical Anthropology Wiley Periodicals LLC 104 S25 66 doi 10 1002 SICI 1096 8644 1997 25 3C63 AID AJPA3 3E3 0 CO 2 8 hdl 2027 42 37682 ISSN 0002 9483 Retrieved 17 January 2024 William Wordsworth for example praised the concept of neoteny in 1802 with words of innocence and hope Kollmann J 1885 Das Ueberwintern von europaischen Frosch und Tritonlarven und die Umwandlung des mexikanischen Axolotl The overwintering of European frog and triton larvae and the transformation of the Mexican axolotl Verhandlungen der Naturforschenden Gesellschaft in Basel Proceedings of the Natural Science Society of Basel in German 7 387 398 From pp 397 398 Dann drangt sich die Frage auf ob das Latenzstadium der Eier das einerseits bei Fischen Vogeln and Saugethieren in so hochst uberraschenden Formen vorkommt anderseits das Latenzstadium bei den Wirbellosen nicht eine Variante derselben Eigenschaft der Organismen sei welche ich Neotenie genannt habe und die auf irgend einer Entwichlungsstufe in Kraft treten kann Then the question arises whether on the one hand the latency stage of eggs which occurs in such highly surprising forms in fish birds and mammals and on the other hand the latency stage in invertebrates be not a variant of the same property of the organisms which I have called neoteny and which can come into force at any stage of development a b c d Bogin Barry 1999 Patterns of Human Growth Cambridge University Press pp 157 169 ISBN 978 0 521 56438 0 Neoteny The Free Dictionary 2011 Accessed April 30 2011 Henke W 2007 Handbook of paleoanthropology Volume 1 Springer Books NY Hetherington R 2010 The Climate Connection Climate Change and Modern Human Evolution Cambridge University Press Hall B K Hallgrimsson B Monroe W S 2008 Strickberger s evolution the integration of genes organisms and populations Jones and Bartlett Publishers Canada Bolk Louis 1926 Das Problem der Menschwerdung Vortrag gehalten am 15 April 1926 auf der XXV Versammlung der anatomischen Gesellschaft zu Freiburg The Problem of Humanization Lecture held on 15 April 1926 at the 25th Congress of the Anatomical Society at Freiberg in German Jena Germany Gustav Fischer Gould Stephen Jay 1977 Ontogeny and Phylogeny Cambridge Massachusetts Belknap Harvard University Press ISBN 978 0 674 63940 9 Shea Brian T 1989 Heterochrony in human evolution The case for neoteny reconsidered American Journal of Physical Anthropology 32 S10 69 101 doi 10 1002 ajpa 1330320505 Thiessen D D 1997 Bittersweet destiny the stormy evolution of human behavior Transaction Publishers N J Jones D et al 1995 Sexual selection physical attractiveness and facial neoteny Cross cultural evidence and implications and comments and reply Current Anthropology 36 5 723 748 doi 10 1086 204427 S2CID 52840802 a b Price E 1999 Behavioral development in animals undergoing domestication Applied Animal Behaviour Science 65 3 245 271 doi 10 1016 S0168 1591 99 00087 8 Bertone J 2006 Equine geriatric medicine and surgery Saunders MI Trut L N 1999 Early canid domestication the farm fox experiment American Scientist 87 2 160 169 Bibcode 1999AmSci 87 T doi 10 1511 1999 2 160 a b McGreevy P D amp Nicholas F W 1999 Some Practical Solutions to Welfare Problems in Dog Breeding In Animal Welfare 8 329 341 Beck A M amp Katcher A H 1996 Between Pets and People The Importance of Companionship West Lafayette Indiana Purdue University Press ISBN 1 55753 077 7 Drake Abby Grace Evolution and development of the skull morphology of canids An investigation of morphological integration and heterochrony January 1 2004 Doctoral Dissertations Available from Proquest Paper AAI3136721 link Drake Abby Grace 2011 Dispelling dog dogma An investigation of heterochrony in dogs using 3D geometric morphometric analysis of skull shape Evolution amp Development 13 2 204 213 doi 10 1111 j 1525 142X 2011 00470 x PMID 21410876 S2CID 20893501 a b Swingle W 1922 Experiments on the metamorphosis of neotenous amphibians Journal of Experimental Zoology 36 4 397 421 doi 10 1002 jez 1400360402 Ambystoma tigrinum Amphibia Web Foster M 1987 Delayed maturation neoteny and social system differences in two manakins of genus Chiroxyphia Evolution 41 3 547 558 doi 10 2307 2409256 JSTOR 2409256 PMID 28563802 a b c Barbosa P et al 1989 Life history traits of forest inhabiting flightless Lepidoptera American Midland Naturalist 122 2 262 274 doi 10 2307 2425912 JSTOR 2425912 a b Harrison R 1980 Dispersal polymorphisms in insects Annual Review of Ecology and Systematics 11 95 118 doi 10 1146 annurev es 11 110180 000523 JSTOR 2096904 a b Snyder R 1956 Comparative Features of the Life Histories of Ambystoma gracile Baird from Populations at Low and High Altitudes Copeia 1956 1 41 50 doi 10 2307 1439242 JSTOR 1439242 a b Shea B T 1983 Paedomorphosis and Neoteny in the Pygmy Chimpanzee Science 222 4623 521 522 Bibcode 1983Sci 222 521S doi 10 1126 science 6623093 JSTOR 1691380 PMID 6623093 Harrison R 1980 Dispersal Polymorphisms in Insects Annual Review of Ecology and Systematics 11 95 118 doi 10 1146 annurev es 11 110180 000523 JSTOR 2096904 Jordal B H Beaver R A Normark B B Farrell B D 2002 Extraordinary sex ratios and the evolution of male neoteny in sib mating Ozopemon beetles Biological Journal of the Linnean Society 75 3 353 360 doi 10 1046 j 1095 8312 2002 00025 x Soltani Mazouni N Bordereau C 1987 Changes in the cuticle ovaries and colleterial glands during the pseudergate and neotenic molt in Kalotermes flavicollis FABR Isoptera Kalotermitidae International Journal of Insect Morphology and Embryology 16 3 4 221 225 doi 10 1016 0020 7322 87 90022 5 Eagleson G McKeown B 1978 Changes in thyroid activity of Ambystoma gracile Baird during different larval transforming and postmetamorphic phases Canadian Journal of Zoology 56 6 1377 1381 doi 10 1139 z78 190 Brokeland W Brandt A 2004 Two new species of Ischnomesidae Crustacea Isopoda from the Southern Ocean displaying neoteny Deep Sea Research Part II 51 14 16 1769 1785 Bibcode 2004DSRII 51 1769B doi 10 1016 j dsr2 2004 06 034 Avidor Reiss Tomer Turner Katerina 2019 Kloc Malgorzata ed The Evolution of Centriole Structure Heterochrony Neoteny and Hypermorphosis The Golgi Apparatus and Centriole Functions Interactions and Role in Disease Results and Problems in Cell Differentiation Cham Springer International Publishing vol 67 pp 3 15 doi 10 1007 978 3 030 23173 6 1 ISBN 978 3 030 23173 6 PMC 7576685 PMID 31435789 retrieved 2023 10 12Further reading editBergstorm Carl T amp Dugatkin Lee Alan 2012 Evolution W W Norton ISBN 039391349XExternal links editSinger Emily 2015 06 02 How Dinosaurs Shrank and Became Birds Quanta Magazine Retrieved from https en wikipedia org w index php title Neoteny amp oldid 1204302174, wikipedia, wiki, book, books, library,

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