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Precociality and altriciality

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Precocial species in birds and mammals are those in which the young are relatively mature and mobile from the moment of birth or hatching. They are normally nidifugous, meaning that they leave the nest shortly after birth or hatching. Altricial species are those in which the young are underdeveloped at the time of birth, but with the aid of their parents mature after birth. These categories form a continuum, without distinct gaps between them.

A diagram of altricial and precocial bird species

In fish, this often refers to the presence or absence of a stomach: precocial larvae have one at the onset of first feeding whereas altricial fish do not.[1] Depending on the species, the larvae may develop a functional stomach during metamorphosis (gastric) or remain stomachless (agastric).

Altricial young birds
California quail chick (Callipepla californica), a precocial chick

Precociality

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Precocial young have open eyes, hair or down, large brains, and are immediately mobile and somewhat able to flee from or defend themselves against predators. For example, with ground-nesting birds such as ducks or turkeys, the young are ready to leave the nest in one or two days. Among mammals, most ungulates are precocial, being able to walk almost immediately after birth.

Etymology

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The word "precocial" is derived from the Latin root praecox, the same root as in precocious, meaning early maturity.[2]

Superprecociality

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Extremely precocial species are called "superprecocial". Examples are the megapode birds, which have full-flight feathers at hatching and which, in some species, can fly on the same day.[3] Enantiornithes[4] and pterosaurs[citation needed] were also capable of flight soon after hatching.

Another example is the blue wildebeest, the calves of which can stand within an average of six minutes from birth and walk within thirty minutes;[5][6] they can outrun a hyena within a day.[7][8][9] Such behavior gives them an advantage over other herbivore species and they are 100 times more abundant in the Serengeti ecosystem than hartebeests, their closest taxonomic relative. Hartebeest calves are not as precocial as wildebeest calves and take up to thirty minutes or more before they stand, and as long as forty-five minutes before they can follow their mothers for short distances. They are unable to keep up with their mothers until they are more than a week old.[9]

Black mambas are highly precocial; as hatchlings, they are fully independent, and are capable of hunting prey the size of a small rat.[10]

Phylogeny

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Precociality is thought to be ancestral in birds. Thus, altricial birds tend to be found in the most derived groups. There is some evidence for precociality in protobirds[11] and troodontids.[12] Enantiornithes at least were superprecocial in a way similar to that of megapodes, being able to fly soon after birth.[4] It has been speculated that superprecociality prevented enantiornithines from acquiring specialized toe anatomy seen in modern altricial birds.[13]

Altriciality

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A human baby, the best-known altricial young

In birds and mammals altricial species are those whose newly hatched or born young are relatively immobile, lack hair or down, are not able to obtain food on their own, and must be cared for by adults; closed eyes are common, though not ubiquitous. Altricial young are born helpless and require care for a length of time. Altricial birds include hawks, herons, woodpeckers, owls, cuckoos and most passerines. Among mammals, marsupials and most rodents are altricial. Domestic cats, dogs, and primates, such as humans, are some of the best-known altricial organisms.[14] For example, newborn domestic cats cannot see, hear, maintain their own body temperature, or gag, and require external stimulation in order to defecate and urinate.[15] The giant panda is notably the largest placental mammal to have altricial, hairless young upon birth. The larval stage of insect development is considered by some to be a form of altricial development, but it more accurately depicts, especially amongst eusocial animals, an independent phase of development, as the larvae of bees, ants, and many arachnids are completely physically different from their developed forms, and the pre-pupal stages of insect life might be regarded as equivalent to vertebrate embryonic development.

Etymology

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The word “altriciality” is derived from the Latin root alere, meaning "to nurse, to rear, or to nourish", and indicates the need for young to be fed and taken care of for a long duration.[16]

Differences

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The span between precocial and altricial species is particularly broad in the biology of birds. Precocial birds hatch with their eyes open and are covered with downy feathers that are soon replaced by adult-type feathers.[17] Birds of this kind can also swim and run much sooner after hatching than altricial young, such as songbirds.[17] Very precocial birds can be ready to leave the nest in a short period of time following hatching (e.g. 24 hours). Many precocial chicks are not independent in thermoregulation (the ability to regulate their body temperatures), and they depend on the attending parent(s) to brood them with body heat for a short time. Precocial birds find their own food, sometimes with help or instruction from their parents. Examples of precocial birds include the domestic chicken, many species of ducks and geese, waders, rails, and the hoatzin.

Precocial birds can provide protein-rich eggs and thus their young hatch in the fledgling stage – able to protect themselves from predators and the females have less post-natal involvement. Altricial birds are less able to contribute nutrients in the pre-natal stage; their eggs are smaller and their young are still in need of much attention and protection from predators. This may be related to r/K selection; however, this association fails in some cases.[18]

In birds, altricial young usually grow faster than precocial young. This is hypothesized to occur so that exposure to predators during the nestling stage of development can be minimized.[19]

In the case of mammals, it has been suggested that large, hearty adult body sizes favor the production of large, precocious young, which develop with a longer gestation period. Large young may be associated with migratory behavior, extended reproductive period, and reduced litter size. It may be that altricial strategies in mammals, in contrast, develop in species with less migratory and more territorial lifestyles, such as Carnivorans, the mothers of which are capable of bearing a fetus in the early stages of development and focusing closely and personally upon its raising, as opposed to precocial animals which provide their youths with a bare minimum of aid and otherwise leave them to instinct.[20]

Human children, and those of other primates, exemplify a unique combination of altricial and precocial development. Infants are born with minimal eyesight, compact and fleshy bodies, and "fresh" features (thinner skin, small noses and ears, and scarce hair if any). However, this stage is only brief amongst primates; their offspring soon develop stronger bones, grow in spurts, and quickly mature in features. This unique growth pattern allows for the hasty adaptivity of most simians, as anything learned by children in between their infancy and adolescence is memorized as instinct; this pattern is also in contrast to more prominently altricial mammals, such as many rodents, which remain largely immobile and undeveloped until grown to near the stature of their parents. [citation needed]

Terminology

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In birds, the terms Aves altrices and Aves precoces were introduced by Carl Jakob Sundevall (1836), and the terms nidifugous and nidicolous by Lorenz Oken in 1816. The two classifications were considered identical in early times, but the meanings are slightly different, in that "altricial" and "precocial" refer to developmental stages, while "nidifugous" and "nidicolous" refer to leaving or staying at the nest, respectively.[18]

See also

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References

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  1. ^ Rønnestad, Ivar; Yúfera, Manuel; Ueberschär, Bernd; Ribeiro, Laura; Saele, Øystein; Boglione, Clara (May 2013). "Feeding behaviour and digestive physiology in larval fish: current knowledge, and gaps and bottlenecks in research". Reviews in Aquaculture. 5: S59–S98. doi:10.1111/raq.12010. hdl:2108/99721.
  2. ^ Webster's New World Dictionary. David B. Guralnik, Editor in Chief. New York: Simon & Schuster, 1984.
  3. ^ Starck, J.M.; Ricklefs, R.E. (1998). Avian Growth and Development. Evolution within the altricial precocial spectrum. New York: Oxford University Press. ISBN 0-19-510608-3.
  4. ^ a b https://www.researchgate.net/publication/338355119_First_report_of_immature_feathers_in_juvenile_enantiornithines_from_the_Early_Cretaceous_Jehol_avifauna; "These feather traces and the plumage in HPG-15-1 strongly suggest that members of the Enantiornithes were born fully fledged and capable of flight soon after hatching, somewhat resembling the super-precocial megapodes, the only group of neornithines in which neonates are similarly born fledged and capable of flight (Zhou and Zhang, 2004; Jones and Göth, 2008; Xing et al., 2017). Megapodes do not fly immediately, requiring nearly two days to dig themselves out of their mounds during which they preen off their feather sheaths and let their feathers dry (Jones and Göth, 2008). Similarly, hatchling enantiornithines would have had to wait until their feather sheaths were removed and their feathers dry before attempting flight. Although ecological and behavioural differences exist between enantiornithines and megapodes (e.g., enantiornithines were arboreal and not mound-nesters), megapodes represent the precocial extreme in extant neornithines and thus the closest analogue for enantiornithine development, for which all evidence indicates a form of extreme precociality (Elzanowski, 1981; Zhou and Zhang, 2004; Xing et al., 2017). "
  5. ^ Estes, R., and E. O. Wilson (1992). The behavior guide to African mammals: Including hoofed mammals, carnivores, primates. Los Angeles: University of California Press
  6. ^ Sinclair, A.R.E., Simon A.R. Mduma, and Peter Arcese (2000). "What determines phenology and synchrony of ungulate breeding in Serengeti?" Ecology 81 (8): 2100–211
  7. ^ Kruuk, H. (1972). The spotted hyena: A study of predation and social behavior. Chicago: University of Chicago
  8. ^ Estes, R.D., and R.K. Estes (1979). "The birth and survival of wildebeest calves". Zeitschrift für Tierpsychologie 50 (1):45
  9. ^ a b Hopcraft, J.G.C.; Sinclair, A.; Holdo, R.M.; Mwangomo, E.; Mduma, S.; Thirgood, S.; Borner, M.; Fryxell, J.M.; Olff, H. (2013). "Why are wildebeest the most abundant herbivore in the Serengeti ecosystem?" (PDF). Serengeti IV: Sustaining Biodiversity in a Coupled Human – Natural System. Chicago: University of Chicago Press. Archived from the original (PDF) on 2011-12-07.
  10. ^ "Snake (Black Mamba)". Better Planet Education. 2014-09-10. Retrieved 2024-09-30.
  11. ^ Elzanowski, Andrzej; Brett-Surman, Michael K. (July 1995). "Avian Premaxilla and Tarsometatarsus from the Uppermost Cretaceous of Montana". The Auk. 112 (3): 762–67. JSTOR 4088693.
  12. ^ Varricchio, David J.; Horner, John R.; Jackson, Frankie D. (September 19, 2002). "Embryos and eggs for the Cretaceous theropod dinosaur Troodon formosus". Journal of Vertebrate Paleontology. 22 (3): 564–76. doi:10.1671/0272-4634(2002)022[0564:EAEFTC]2.0.CO;2. JSTOR 4524250. S2CID 85728452.
  13. ^ Clark, Alexander D.; o'Connor, Jingmai K. (2021). "Exploring the Ecomorphology of Two Cretaceous Enantiornithines with Unique Pedal Morphology". Frontiers in Ecology and Evolution. 9. doi:10.3389/fevo.2021.654156.
  14. ^ Arterberry, Martha E. (2000). The Cradle of Knowledge. Development of Perception in Infancy. Cambridge: MIT Press. p. 27. ISBN 9780262611527.
  15. ^ Hannah Shaw. "Determining a Kitten's Age".
  16. ^ Ehrlich, Paul (1988). The Birder's Handbook. New York: Simon & Schuster. ISBN 0-671-65989-8.[page needed]
  17. ^ a b Edward S. Brinkley (2000). Creatures of the Air and Sea. Singapore: Reader's Digest Children's Books. pp. 34, 35. ISBN 0-7944-0353-0.
  18. ^ a b Starck, J. (1998). Avian Growth and Development. Oxford Oxfordshire: Oxford University Press. ISBN 0-19-510608-3.[page needed]
  19. ^ Kahl, M. Philip (1962). "Bioenergetics of growth in nestling wood storks". The Condor. 64 (3): 169–183. doi:10.2307/1365200. ISSN 0010-5422. JSTOR 1365200.
  20. ^ Eisenberg, John (1981). The Mammalian Radiations. London: Athlone Press. ISBN 0-485-30008-7.[page needed]

Bibliography

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  • Starck J.M.; Ricklefs R.E. (1998). "Patterns of Development: The Altricial – Precocial Spectrum". Avian Growth and Development. New York: Oxford University Press.
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