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Snake
Snake
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Snake
Temporal range:
Late CretaceousPresent,[1] 94–0 Ma
Trimeresurus sabahi
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Order: Squamata
Clade: Toxicofera
Clade: Ophidia
Suborder: Serpentes
Linnaeus, 1758
Infraorders
Approximate world distribution of snakes, all species

Snakes are elongated limbless reptiles of the suborder Serpentes (/sɜːrˈpɛntz/).[2] Cladistically squamates, snakes are ectothermic, amniote vertebrates covered in overlapping scales much like other members of the group. Many species of snakes have skulls with several more joints than their lizard ancestors and relatives, enabling them to swallow prey much larger than their heads (cranial kinesis). To accommodate their narrow bodies, snakes' paired organs (such as kidneys) appear one in front of the other instead of side by side, and most only have one functional lung. Some species retain a pelvic girdle with a pair of vestigial claws on either side of the cloaca. Lizards have independently evolved elongate bodies without limbs or with greatly reduced limbs at least twenty-five times via convergent evolution, leading to many lineages of legless lizards.[3] These resemble snakes, but several common groups of legless lizards have eyelids and external ears, which snakes lack, although this rule is not universal (see Amphisbaenia, Dibamidae, and Pygopodidae).

Living snakes are found on every continent except Antarctica, and on most smaller land masses; exceptions include some large islands, such as Ireland, Iceland, Greenland, and the islands of New Zealand, as well as many small islands of the Atlantic and central Pacific oceans.[4] Additionally, sea snakes are widespread throughout the Indian and Pacific oceans. Around thirty families are currently recognized, comprising about 520 genera and about more than 4,170 species.[5] They range in size from the tiny, 10.4 cm-long (4.1 in) Barbados threadsnake[6] to the reticulated python of 6.95 meters (22.8 ft) in length.[7] The fossil species Titanoboa cerrejonensis was 12.8 meters (42 ft) long.[8] Snakes are thought to have evolved from either burrowing or aquatic lizards, perhaps during the Jurassic period, with the earliest known fossils dating to between 143 and 167 Ma ago.[9][10] The diversity of modern snakes appeared during the Paleocene epoch (c. 66 to 56 Ma ago, after the Cretaceous–Paleogene extinction event). The oldest preserved descriptions of snakes can be found in the Brooklyn Papyrus.

Most species of snake are nonvenomous and those that have venom use it primarily to kill and subdue prey rather than for self-defense. Some possess venom that is potent enough to cause painful injury or death to humans. Nonvenomous snakes either swallow prey alive or kill by constriction.

Etymology

[edit]

The English word snake comes from Old English snaca, itself from Proto-Germanic *snak-an- (cf. Germanic Schnake 'ring snake', Swedish snok 'grass snake'), from Proto-Indo-European root *(s)nēg-o- 'to crawl to creep', which also gave sneak as well as Sanskrit nāgá 'snake'.[11] The word ousted adder, as adder went on to narrow in meaning, though in Old English næddre was the general word for snake.[12] The other term, serpent, is from French, ultimately from Indo-European *serp- 'to creep',[13] which also gave Ancient Greek ἕρπω (hérpō) 'I crawl' and Sanskrit sarpá 'snake'.[14]

Taxonomy

[edit]

All modern snakes are grouped within the suborder Serpentes in Linnean taxonomy, part of the order Squamata, though their precise placement within squamates remains controversial.[15]

The two infraorders of Serpentes are Alethinophidia and Scolecophidia.[15] This separation is based on morphological characteristics and mitochondrial DNA sequence similarity. Alethinophidia is sometimes split into Henophidia and Caenophidia, with the latter consisting of "colubroid" snakes (colubrids, vipers, elapids, hydrophiids, and atractaspids) and acrochordids, while the other alethinophidian families comprise Henophidia.[16] While not extant today, the Madtsoiidae, a family of giant, primitive, python-like snakes, lived until 50,000 years ago in Australia, represented by genera such as Wonambi.[17]

Recent molecular studies support the monophyly of the clades of modern snakes, scolecophidians, typhlopids + anomalepidids, alethinophidians, core alethinophidians, uropeltids (Cylindrophis, Anomochilus, uropeltines), macrostomatans, booids, boids, pythonids and caenophidians.[18]

Families

[edit]
Infraorder Alethinophidia 25 families
Family[5] Taxon author[5] Genera[5] Species[5] Common name Geographic range[19]
Acrochordidae Bonaparte, 1831 1 3 Wart snakes Western India and Sri Lanka through tropical Southeast Asia to the Philippines, south through the Indonesian/Malaysian island group to Timor, east through New Guinea to the northern coast of Australia to Mussau Island, the Bismarck Archipelago and Guadalcanal Island in the Solomon Islands.
Aniliidae Stejneger, 1907 1 1 False coral snake Tropical South America.
Anomochilidae Cundall, Wallach, 1993 1 3 Dwarf pipe snakes West Malaysia and on the Indonesian island of Sumatra.
Atractaspididae Günther, 1858 12 72 Burrowing asps Africa and the Middle East
Boidae Gray, 1825 14 61 Boas Northern, Central and South America, the Caribbean, southeastern Europe and Asia Minor, Northern, Central and East Africa, Madagascar and Reunion Island, the Arabian Peninsula, Central and southwestern Asia, India and Sri Lanka, the Moluccas and New Guinea through to Melanesia and Samoa.
Bolyeriidae Hoffstetter, 1946 2 2 Splitjaw snakes Mauritius.
Colubridae Oppel, 1811 258[5] 2055[5] Typical snakes Widespread on all continents, except Antarctica.[20]
Cyclocoridae Weinell & Brown, 2017 5 8 Cyclocorids The Philippines
Cylindrophiidae Fitzinger, 1843 1 14 Asian pipe snakes Sri Lanka east through Myanmar, Thailand, Cambodia, Vietnam and the Malay Archipelago to as far east as Aru Islands off the southwestern coast of New Guinea. Also found in southern China (Fujian, Hong Kong and on Hainan Island) and in Laos.
Elapidae Boie, 1827 55 389 Elapids On land, worldwide in tropical and subtropical regions, except in Europe. Sea snakes occur in the Indian Ocean and the Pacific.[21]
Homalopsidae Bonaparte, 1845 28 53 Homalopsids Southeastern Asia and northern Australia.
Lamprophiidae Fitzinger, 1843 16 89 Lamprophiids (formerly included Atracaspididae, Psammophiidae, and several other families) Africa (including the Seychelles)
Loxocemidae Cope, 1861 1 1 Mexican burrowing snake Along the Pacific versant from Mexico south to Costa Rica.
Micrelapidae Das et al., 2023 1 4 Two-headed snakes Eastern Africa and the Levant
Pareidae Romer, 1956 3 20 Snail-eating snakes Southeast Asia and islands on the Sunda Shelf (Sumatra, Borneo, Java, and their surrounding smaller islands).
Prosymnidae Kelly, Barker, Villet & Broadley, 2009 1 16 Shovel-snout snakes Subsaharan Africa
Psammodynastidae Das et al., 2024 1 2 Mock vipers Tropical Asia
Psammophiidae Bourgeois, 1968 8 55 Psammophiids Africa (including Madagascar), Asia and southern Europe
Pseudaspididae Cope, 1893 2 2 Pseudaspidids Subsaharan Africa
Pseudoxyrhophiidae Dowling, 1975 22 89 Pseudoxyrhophiids Mostly Madagascar and the Comoros; 5 species in subsaharan Africa, 1 in Socotra
Pythonidae Fitzinger, 1826 8 40 Pythons Subsaharan Africa, India, Myanmar, southern China, Southeast Asia and from the Philippines southeast through Indonesia to New Guinea and Australia.
Tropidophiidae Brongersma, 1951 2 34 Dwarf boas West Indies; also Panama and northwestern South America, as well as in northwestern and southeastern Brazil.
Uropeltidae Müller, 1832 8 55 Shield-tailed snakes Southern India and Sri Lanka.
Viperidae Oppel, 1811 35 341 Vipers The Americas, Africa, and Eurasia east to Wallace's Line.
Xenodermidae Cope, 1900 6 18 Dragon and odd-scaled snakes East Asia, Southern and southeastern Asia, and islands on the Sunda Shelf (Sumatra, Borneo, Java, and their surrounding smaller islands).
Xenopeltidae Bonaparte, 1845 1 2 Sunbeam snakes Southeast Asia from the Andaman and Nicobar Islands, east through Myanmar to southern China, Thailand, Laos, Cambodia, Vietnam, the Malay Peninsula and the East Indies to Sulawesi, as well as the Philippines.
Xenophidiidae Wallach & Günther, 1998 1 2 Spine-jawed snakes Borneo and peninsular Malaysia.


Infraorder Scolecophidia 5 families
Family[5] Taxon author[5] Genera[5] Species[5] Common name Geographic range[19]
Anomalepidae Taylor, 1939 4 18 Primitive blind snakes From southern Central America to northwestern South America. Disjunct populations in northeastern and southeastern South America.
Gerrhopilidae Vidal, Wynn, Donnellan and Hedges 2010 2 18 Indo-Malayan blindsnakes Southern and southeastern Asia, including Sri Lanka, the Philippines, and New Guinea.
Leptotyphlopidae Stejneger, 1892 13 139 Slender blind snakes Africa, western Asia from Turkey to northwestern India, on Socotra Island, from the southwestern United States south through Mexico and Central to South America, though not in the high Andes. In Pacific South America they occur as far south as southern coastal Peru, and on the Atlantic side as far as Uruguay and Argentina. In the Caribbean they are found on the Bahamas, Hispaniola and the Lesser Antilles.
Typhlopidae Merrem, 1820 18 266 Typical blind snakes Most tropical and many subtropical regions around the world, particularly in Africa, Madagascar, Asia, islands in the Pacific, tropical America and in southeastern Europe.
Xenotyphlopidae Vidal, Vences, Branch and Hedges 2010 1 1 Round-nosed blindsnake Northern Madagascar.

Legless lizards

[edit]

While snakes are limbless reptiles, evolved from (and grouped with) lizards, there are many other species of lizards that have lost their limbs independently but which superficially look similar to snakes. These include the slowworm, glass snake, and amphisbaenians.[22]

Evolution

[edit]
Unsolved problem in biology
Did snakes evolve from burrowing lizards or aquatic lizards?
A family level phylogenetic overview of modern snakes.
Note: the tree only indicates relationships, not evolutionary branching times. This is not a definitive tree. It is the best that could be done as of 2024. See original paper for a discussion of difficulties.[23]
Snakes

The fossil record of snakes is relatively poor because snake skeletons are typically small and fragile making fossilization uncommon. Fossils readily identifiable as snakes (though often retaining hind limbs) first appear in the fossil record during the Cretaceous period.[24] The earliest known true snake fossils (members of the crown group Serpentes) come from the marine simoliophiids, the oldest of which is the Late Cretaceous (Cenomanian age) Haasiophis terrasanctus from the West Bank,[1] dated to between 112 and 94 million years old.[25]

Based on genomic analysis it is certain that snakes descend from lizards.[23] This conclusion is also supported by comparative anatomy, and the fossil record.[26]: 11 [27][23]

Pythons and boas—primitive groups among modern snakes—have vestigial hind limbs: tiny, clawed digits known as anal spurs, which are used to grasp during mating.[26]: 11 [28] The families Leptotyphlopidae and Typhlopidae also possess remnants of the pelvic girdle, appearing as horny projections when visible.

Front limbs are nonexistent in all known snakes. This is caused by the evolution of their Hox genes, controlling limb morphogenesis. The axial skeleton of the snakes' common ancestor, like most other tetrapods, had regional specializations consisting of cervical (neck), thoracic (chest), lumbar (lower back), sacral (pelvic), and caudal (tail) vertebrae. Early in snake evolution, the Hox gene expression in the axial skeleton responsible for the development of the thorax became dominant. As a result, the vertebrae anterior to the hindlimb buds (when present) all have the same thoracic-like identity (except from the atlas, axis, and 1–3 neck vertebrae). In other words, most of a snake's skeleton is an extremely extended thorax. Ribs are found exclusively on the thoracic vertebrae. Neck, lumbar and pelvic vertebrae are very reduced in number (only 2–10 lumbar and pelvic vertebrae are present), while only a short tail remains of the caudal vertebrae. However, the tail is still long enough to be of important use in many species, and is modified in some aquatic and tree-dwelling species.[citation needed]

Many modern snake groups originated during the Paleocene, alongside the adaptive radiation of mammals following the extinction of (non-avian) dinosaurs. The expansion of grasslands in North America also led to an explosive radiation among snakes.[29] Previously, snakes were a minor component of the North American fauna, but during the Miocene, the number of species and their prevalence increased dramatically with the first appearances of vipers and elapids in North America and the significant diversification of Colubridae (including the origin of many modern genera such as Nerodia, Lampropeltis, Pituophis, and Pantherophis).[29]

Fossils

[edit]

There is fossil evidence to suggest that snakes may have evolved from burrowing lizards during the Cretaceous Period.[30][31] An early fossil snake relative, Najash rionegrina, was a two-legged burrowing animal with a sacrum, and was fully terrestrial.[32] Najash, which lived 95 million years ago, also had a skull with several features typical for lizards, but had evolved some of the mobile skull joints that define the flexible skull in most modern snakes. The species did not show any resemblances to the modern burrowing blind snakes, which have often been seen as the most primitive group of extant forms.[33] One extant analog of these putative ancestors is the earless monitor Lanthanotus of Borneo (though it is also semiaquatic).[34] Subterranean species evolved bodies streamlined for burrowing, and eventually lost their limbs.[34] According to this hypothesis, features such as the transparent, fused eyelids (brille) and loss of external ears evolved to cope with fossorial difficulties, such as scratched corneas and dirt in the ears.[31][34] Some primitive snakes are known to have possessed hindlimbs, but their pelvic bones lacked a direct connection to the vertebrae. These include fossil species like Haasiophis, Pachyrhachis and Eupodophis, which are slightly older than Najash.[28]

This hypothesis was strengthened in 2015 by the discovery of a 113-million-year-old fossil of a four-legged snake in Brazil that has been named Tetrapodophis amplectus. It has many snake-like features, is adapted for burrowing and its stomach indicates that it was preying on other animals.[35] It is currently uncertain if Tetrapodophis is a snake or another species, in the squamate order, as a snake-like body has independently evolved at least 26 times. Tetrapodophis does not have distinctive snake features in its spine and skull.[36][37] A study in 2021 places the animal in a group of extinct marine lizards from the Cretaceous period known as dolichosaurs and not directly related to snakes.[38]

An alternative hypothesis, based on morphology, suggests the ancestors of snakes were related to mosasaurs—extinct aquatic reptiles from the Cretaceous—forming the clade Pythonomorpha.[27] According to this hypothesis, the fused, transparent eyelids of snakes are thought to have evolved to combat marine conditions (corneal water loss through osmosis), and the external ears were lost through disuse in an aquatic environment. This ultimately led to an animal similar to today's sea snakes. In the Late Cretaceous, snakes recolonized land, and continued to diversify into today's snakes. Fossilized snake remains are known from early Late Cretaceous marine sediments, which is consistent with this hypothesis; particularly so, as they are older than the terrestrial Najash rionegrina. Similar skull structure, reduced or absent limbs, and other anatomical features found in both mosasaurs and snakes lead to a positive cladistical correlation, although some of these features are shared with varanids.[citation needed]

Genetic studies in recent years have indicated snakes are not as closely related to monitor lizards as was once believed—and therefore not to mosasaurs, the proposed ancestor in the aquatic scenario of their evolution. However, more evidence links mosasaurs to snakes than to varanids. Fragmented remains found from the Jurassic and Early Cretaceous indicate deeper fossil records for these groups, which may potentially refute either hypothesis.[39][40]

Genetic basis of snake evolution

[edit]

Both fossils and phylogenetic studies demonstrate that snakes evolved from lizards, hence the question became which genetic changes led to limb loss in the snake ancestor. Limb loss is actually very common in extant reptiles and has happened dozens of times within skinks, anguids, and other lizards.[41]

In 2016, two studies reported that limb loss in snakes is associated with DNA mutations in the Zone of Polarizing Activity Regulatory Sequence (ZRS), a regulatory region of the sonic hedgehog gene which is critically required for limb development. More advanced snakes have no remnants of limbs, but basal snakes such as pythons and boas do have traces of highly reduced, vestigial hind limbs. Python embryos even have fully developed hind limb buds, but their later development is stopped by the DNA mutations in the ZRS.[42][43][44][45]

Distribution

[edit]
Approximate world distribution of snakes

There are about 3,900 species of snakes,[46] ranging as far northward as the Arctic Circle in Scandinavia and southward through Australia.[27] Snakes can be found on every continent except Antarctica, as well as in the sea, and as high as 16,000 feet (4,900 m) in the Himalayan Mountains of Asia.[27][47]: 143  There are numerous islands from which snakes are absent, such as Ireland, Iceland, and New Zealand[4][47] (although New Zealand's northern waters are infrequently visited by the yellow-bellied sea snake and the banded sea krait).[48]

Biology

[edit]
An adult Barbados threadsnake, Leptotyphlops carlae, on an American quarter dollar

Size

[edit]

The now extinct Titanoboa cerrejonensis was 12.8 m (42 ft) in length.[8] By comparison, the largest extant snakes are the reticulated python, measuring about 6.95 m (22.8 ft) long,[7] and the green anaconda, which measures about 5.21 m (17.1 ft) long and is considered the heaviest snake on Earth at 97.5 kg (215 lb).[49]

At the other end of the scale, the smallest extant snake is Leptotyphlops carlae, with a length of about 10.4 cm (4.1 in).[6] Most snakes are fairly small animals, approximately 1 m (3.3 ft) in length.[50]

Perception

[edit]

The sensory systems of snakes, particularly those of the Crotalidae family, commonly known as pit vipers, are among the most specialized in the animal kingdom. Pit vipers, which include rattlesnakes and related species, possess all the sensory organs found in other snakes, as well as additional adaptations. These include specialized infrared-sensitive receptors, known as pits, located on either side of the head between the nostrils and eyes. These pits, which resemble an additional pair of nostrils, are highly developed and allow pit vipers to detect minute temperature changes. Each pit consists of two cavities: a larger outer cavity positioned just behind and below the nostril, and a smaller inner cavity. These cavities are connected internally by a membrane containing nerves highly sensitive to thermal variations. The forward-facing pits create a combined field of detection, enabling pit vipers to distinguish objects from their surroundings and accurately judge distances. The sensitivity of these pits allows them to detect temperature differences as small as one-third of a degree Fahrenheit. Other infrared-sensitive snakes, such as those in the Boidae family, possess multiple smaller labial pits along the upper lip, just below the nostrils.[51]

Snakes rely heavily on their sense of smell to track prey. They collect particles from the air, ground, or water using their forked tongue, which are then transferred to the vomeronasal organ (also known as Jacobson's organ) in the mouth for analysis.[51] The forked structure of the tongue provides directional information of smell which helps locate prey or predators. In aquatic species, such as the anaconda, the tongue functions efficiently underwater.[51] When the tongue is retracted, the forked tips are pressed into the cavities of the Jacobson's organ, enabling a combined taste-smell analysis that provides the snake with detailed information about its environment.[52][page needed][51]

A line diagram from The Fauna of British India by G. A. Boulenger (1890), illustrating the terminology of shields on the head of a snake

Until the mid-20th century, it was widely believed that snakes were unable to hear.[53][54] However, snakes possess two distinct auditory systems. One system, the somatic system, involves the transmission of vibrations through ventral skin receptors to the spine. The other system involves vibrations transmitted through the snake's elongated lung to the brain via cranial nerves. Snakes exhibit high sensitivity to vibrations, allowing them to detect even subtle sounds, such as soft speech, in quiet environments.[53][51][54]

Snake vision varies significantly among species. While some snakes have keen eyesight, others can only distinguish light from dark. However, most snakes possess visual acuity sufficient to track movement.[55] Arboreal snakes generally have better vision than burrowing species. Some snakes, such as the Asian vine snake, possess binocular vision, enabling both eyes to focus on the same point. Most snakes focus by moving the lens back and forth relative to the retina. Diurnal snakes typically have round pupils, while many nocturnal species have slit pupils. Most snakes possess three visual pigments, allowing them to perceive two primary colors in daylight. Certain species, such as the annulated sea snake and members of the genus Helicops, have regained significant color vision as an adaptation to their aquatic environments.[56][57] Research suggests that the last common ancestor of all snakes had UV-sensitive vision. However, many diurnal snakes have evolved lenses that filter out UV light, likely improving contrast and sharpening their vision.[58][59]

Skin

[edit]

The skin of a snake is covered in scales. Contrary to the popular notion of snakes being slimy (because of possible confusion of snakes with worms), snakeskin has a smooth, dry texture. Most snakes use specialized belly scales to travel, allowing them to grip surfaces. The body scales may be smooth, keeled, or granular. The eyelids of a snake are transparent "spectacle" scales, also known as brille, which remain permanently closed.[citation needed]

For a snake, the skin has been modified to its specialized form of locomotion. Between the inner layer and the outer layer lies the dermis, which contains all the pigments and cells that make up the snake's distinguishing pattern and color. The epidermis, or outer layer, is formed of a substance called keratin, which in mammals is the same basic material that forms nails, claws, and hair. The snake's epidermis of keratin provides it with the armor it needs to protect its internal organs and reduce friction as it passes over rocks. Parts of this keratin armor are rougher than others. The less restricted portion overlaps the front of the scale beneath it. Between them lies a folded back connecting material, also of keratin, also part of the epidermis. This folded back material gives as the snake undulates or eats things bigger than the circumference of its body.[52][page needed]

The shedding of scales is called ecdysis (or in normal usage, molting or sloughing). Snakes shed the complete outer layer of skin in one piece.[60] Snake scales are not discrete, but extensions of the epidermis—hence they are not shed separately but as a complete outer layer during each molt, akin to a sock being turned inside out.[61]

Snakes have a wide diversity of skin coloration patterns which are often related to behavior, such as the tendency to have to flee from predators. Snakes that are at a high risk of predation tend to be plain, or have longitudinal stripes, providing few reference points to predators, thus allowing the snake to escape without being noticed. Plain snakes usually adopt active hunting strategies, as their pattern allows them to send little information to prey about motion. Blotched snakes usually use ambush-based strategies, likely because it helps them blend into an environment with irregularly shaped objects, like sticks or rocks. Spotted patterning can similarly help snakes to blend into their environment.[62]

The shape and number of scales on the head, back, and belly are often characteristic and used for taxonomic purposes. Scales are named mainly according to their positions on the body. In "advanced" (Caenophidian) snakes, the broad belly scales and rows of dorsal scales correspond to the vertebrae, allowing these to be counted without the need for dissection.[citation needed]

Molting

[edit]
A common watersnake shedding its skin

Molting (or "ecdysis") serves a number of purposes - it allows old, worn skin to be replaced and can be synced to mating cycles, as with other animals. Molting occurs periodically throughout the life of a snake. Before each molt, the snake regulates its diet and seeks defensible shelter. Just before shedding, the skin becomes grey and the snake's eyes turn silvery. The inner surface of the old skin liquefies, causing it to separate from the new skin beneath it. After a few days, the eyes clear and the snake reaches out of its old skin, which splits. The snake rubs its body against rough surfaces to aid in the shedding of its old skin. In many cases, the castaway skin peels backward over the body from head to tail in one piece, like taking the dust jacket off a book, revealing a new, larger, brighter layer of skin which has formed underneath.[61][63] Renewal of the skin by molting supposedly increases the mass of some animals such as insects, but in the case of snakes this has been disputed.[61][64] Shedding skin can release pheromones and revitalize color and patterns of the skin to increase attraction of mates.[65]

Shed skin of a snake

Snakes may shed four or five times a year, depending on the weather conditions, food supply, age of the snake, and other factors.[52][page needed][63] It is theoretically possible to identify the snake from its cast skin if it is reasonably intact.[61] Mythological associations of snakes with symbols of healing and medicine, as pictured in the Rod of Asclepius, are derivative of molting.[66]

One can attempt to identify the sex of a snake when the species is not distinctly sexually dimorphic by counting scales. The cloaca is probed and measured against the subcaudal scales.[67] Counting scales determines whether a snake is a male or female, as the hemipenes of a male being probed is usually longer.[67][clarification needed]

Skeleton

[edit]
Reticulated python skull, showing jaw movements when swallowing

The skull of a snake differs from a lizards in several ways. Snakes have more flexible jaws, that is, instead of a juncture at the upper and lower jaw, the snake's jaws are connected by a bone hinge that is called the quadrate bone. Between the two halves of the lower jaw at the chin there is an elastic ligament that allows for a separation. This allows the snake to swallow food larger in proportion to their size and go longer without it, since snakes ingest relatively more in one feeding.[68] Because the sides of the lower jaw can move independently of one another, a snake resting its jaw on a surface has stereo auditory perception, used for detecting the position of prey. The jaw–quadrate–stapes pathway is capable of detecting vibrations on the angstrom scale, despite the absence of an outer ear and the lack of an impedance matching mechanism—provided by the ossicles in other vertebrates.[69][70] In a snake's skull the brain is well protected. As brain tissues could be damaged through the palate, this protection is especially valuable. The solid and complete neurocranium of snakes is closed at the front.[52][page needed][71]

The skeletons of snakes are radically different from those of most other reptiles (as compared with the turtle here, for example), consisting almost entirely of an extended ribcage.

The skeleton of most snakes consists solely of the skull, hyoid, vertebral column, and ribs, though henophidian snakes retain vestiges of the pelvis and rear limbs. The hyoid is a small bone located posterior and ventral to the skull, in the 'neck' region, which serves as an attachment for the muscles of the snake's tongue, as it does in all other tetrapods. The vertebral column consists of between 200 and 400 vertebrae, or sometimes more. The body vertebrae each have two ribs articulating with them. The tail vertebrae are comparatively few in number (often less than 20% of the total) and lack ribs. The vertebrae have projections that allow for strong muscle attachment, enabling locomotion without limbs.[citation needed]

Caudal autotomy (self-amputation of the tail), a feature found in some lizards, is absent in most snakes.[72] In the rare cases where it does exist in snakes, caudal autotomy is intervertebral (meaning the separation of adjacent vertebrae), unlike that in lizards, which is intravertebral, i.e. the break happens along a predefined fracture plane present on a vertebra.[73][74]

In some snakes, most notably boas and pythons, there are vestiges of the hindlimbs in the form of a pair of pelvic spurs. These small, claw-like protrusions on each side of the cloaca are the external portion of the vestigial hindlimb skeleton, which includes the remains of an ilium and femur.[citation needed]

Snakes are polyphyodonts with teeth that are continuously replaced.[75]

Internal organs

[edit]
1: esophagus2: trachea3:tracheal lungs4: rudimentary left lung4: right lung6: heart7: liver8 stomach9: air sac10: gallbladder11: pancreas12: spleen13: intestine14: testicles15: kidneys
Anatomy of a snake.file info
  1. esophagus
  2. trachea
  3. tracheal lungs
  4. rudimentary left lung
  5. right lung
  6. heart
  7. liver
  8. stomach
  9. air sac
  10. gallbladder
  11. pancreas
  12. spleen
  13. intestine
  14. testicles
  15. kidneys

Snakes and other non-archosaur (crocodilians, dinosaurs + birds and allies) reptiles have a three-chambered heart that controls the circulatory system via the left and right atrium, and one ventricle.[76] Internally, the ventricle is divided into three interconnected cavities: the cavum arteriosum, the cavum pulmonale, and the cavum venosum.[77] The cavum venosum receives deoxygenated blood from the right atrium and the cavum arteriosum receives oxygenated blood from the left atrium. Located beneath the cavum venosum is the cavum pulmonale, which pumps blood to the pulmonary trunk.[78]

The snake's heart is encased in a sac, called the pericardium, located at the bifurcation of the bronchi. The heart is able to move around, owing to the lack of a diaphragm; this adjustment protects the heart from potential damage when large ingested prey is passed through the esophagus. The spleen is attached to the gall bladder and pancreas and filters the blood. The thymus, located in fatty tissue above the heart, is responsible for the generation of immune cells in the blood. The cardiovascular system of snakes is unique for the presence of a renal portal system in which the blood from the snake's tail passes through the kidneys before returning to the heart.[79]

The circulatory system of a snake is basically like those of any other vertebrae. However, snakes do not regulate internally the temperature of their blood. Called cold-blooded, snakes actually have blood that is responsive to the varying temperature of the immediate environment. Snakes can regulate blood temperature by moving. Too long in direct sunlight, the snakes' blood is heated beyond tolerance. Left in the ice or snow, the snake may freeze. In temperate zones with pronounced seasonal changes, snakes denning together have adapted to the onslaught of winter.[52][page needed]

The vestigial left lung is often small or sometimes even absent, as snakes' tubular bodies require all of their organs to be long and thin.[79] In the majority of species, only one lung is functional. This lung contains a vascularized anterior portion and a posterior portion that does not function in gas exchange.[79] This 'saccular lung' is used for hydrostatic purposes to adjust buoyancy in some aquatic snakes and its function remains unknown in terrestrial species.[79] Many organs that are paired, such as kidneys or reproductive organs, are staggered within the body, one located ahead of the other.[79]

The snake with its particular arrangement of organs may achieve a greater efficiency.[compared to?] For example, the lung encloses at the part nearest the head and throat an oxygen intake organ, while the other half is used for air reserve. The esophagus-stomach-intestine arrangement is a straight line. It ends where intestinal, urinary, and reproductive tracts open, in a chamber called the cloaca.[52][page needed]

Snakes have no lymph nodes.[79]

Venom

[edit]
Innocuous milk snakes (top) are often mistaken for coral snakes (bottom) whose venom is deadly to humans.

Cobras, vipers, and closely related species use venom to immobilize, injure, or kill their prey. The venom is modified saliva, delivered through fangs.[26][80]: 243  The fangs of 'advanced' venomous snakes like viperids and elapids are hollow, allowing venom to be injected more effectively, and the fangs of rear-fanged snakes such as the boomslang simply have a groove on the posterior edge to channel venom into the wound. Snake venoms are often prey-specific, and their role in self-defense is secondary.[26][80]: 243 

Venom, like all salivary secretions, is a predigestant that initiates the breakdown of food into soluble compounds, facilitating proper digestion. Even nonvenomous snakebites (like any animal bite) cause tissue damage.[26][80]: 209 

Skulls from left to right: Nonvenomous (Pseustes sp.), rear-fanged (Toxicodryas blandingii), elapid (Micropechis ikaheca), viperid (Crotalus adamanteus), venomous lizard (Heloderma suspectum). Maxilla in red.

Certain birds, mammals, and other snakes (such as kingsnakes) that prey on venomous snakes have developed resistance and even immunity to certain venoms.[26]: 243  Venomous snakes include three families of snakes, and do not constitute a formal taxonomic classification group.[citation needed]

The colloquial term "poisonous snake" is generally an incorrect label for snakes. A poison is inhaled or ingested, whereas venom produced by snakes is injected into its victim via fangs.[81] There are, however, two exceptions: Rhabdophis sequesters toxins from the toads it eats, then secretes them from nuchal glands to ward off predators; and a small unusual population of garter snakes in the US state of Oregon retains enough toxins in their livers from ingested newts to be effectively poisonous to small local predators (such as crows and foxes).[82]

Snake venoms are complex mixtures of proteins,[80] and are stored in venom glands at the back of the head.[82] In all venomous snakes, these glands open through ducts into grooved or hollow teeth in the upper jaw.[26]: 243 [81] The proteins can potentially be a mix of neurotoxins (which attack the nervous system), hemotoxins (which attack the circulatory system), cytotoxins (which attack the cells directly), bungarotoxins (related to neurotoxins, but also directly affect muscle tissue), and many other toxins that affect the body in different ways.[81][80] Almost all snake venom contains hyaluronidase, an enzyme that ensures rapid diffusion of the venom.[26]: 243 

Venomous snakes that use hemotoxins usually have fangs in the front of their mouths, making it easier for them to inject the venom into their victims.[80][81] Some snakes that use neurotoxins (such as the mangrove snake) have fangs in the back of their mouths, with the fangs curled backwards.[83] This makes it difficult both for the snake to use its venom and for scientists to milk them.[81] Elapids, however, such as cobras and kraits are proteroglyphous—they possess hollow fangs that cannot be erected toward the front of their mouths, and cannot "stab" like a viper. They must actually bite the victim.[26]: 242 

It has been suggested that all snakes may be venomous to a certain degree, with harmless snakes having weak venom and no fangs.[84] According to this theory, most snakes that are labelled "nonvenomous" would be considered harmless because they either lack a venom delivery method or are incapable of delivering enough to endanger a human. The theory postulates that snakes may have evolved from a common lizard ancestor that was venomous, and also that venomous lizards like the gila monster, beaded lizard, monitor lizards, and the now-extinct mosasaurs, may have derived from this same common ancestor. They share this "venom clade" with various other saurian species.[citation needed]

Venomous snakes are classified in two taxonomic families:

There is a third family containing the opistoglyphous (rear-fanged) snakes (as well as the majority of other snake species):

Reproduction

[edit]
Boa imperator (left) and an albino Python molurus (right). The former gives birth to live young, while the latter lays eggs.

Although a wide range of reproductive modes are used by snakes, all employ internal fertilization. This is accomplished by means of paired, forked hemipenes, which are stored, inverted, in the male's tail.[85] The hemipenes are often grooved, hooked, or spined—designed to grip the walls of the female's cloaca.[86][85] The clitoris of the female snake consists of two structures located between the cloaca and the scent glands.[87]

Most species of snakes lay eggs which they abandon shortly after laying. However, a few species (such as the king cobra) construct nests and stay in the vicinity of the hatchlings after incubation.[85] Most pythons coil around their egg-clutches and remain with them until they hatch.[88] A female python will not leave the eggs, except to occasionally bask in the sun or drink water. She will even "shiver" to generate heat to incubate the eggs.[88]

Some species of snake are ovoviviparous and retain the eggs within their bodies until they are almost ready to hatch.[89][90] Several species of snake, such as the boa constrictor and green anaconda, are fully viviparous, nourishing their young through a placenta as well as a yolk sac; this is highly unusual among reptiles, and normally found in requiem sharks or placental mammals.[89][90] Retention of eggs and live birth are most often associated with colder environments.[85][90]

The garter snake has been studied for sexual selection.

Sexual selection in snakes is demonstrated by the 3,000 species that each use different tactics in acquiring mates.[91] Ritual combat between males for the females they want to mate with includes topping, a behavior exhibited by most viperids in which one male will twist around the vertically elevated fore body of its opponent and force it downward. It is common for neck-biting to occur while the snakes are entwined.[92]

Facultative parthenogenesis

[edit]

Parthenogenesis is a natural form of reproduction in which growth and development of embryos occur without fertilization. Agkistrodon contortrix (copperhead) and Agkistrodon piscivorus (cottonmouth) can reproduce by facultative parthenogenesis, meaning that they are capable of switching from a sexual mode of reproduction to an asexual mode.[93] The most likely type of parthenogenesis to occur is automixis with terminal fusion, a process in which two terminal products from the same meiosis fuse to form a diploid zygote. This process leads to genome-wide homozygosity, expression of deleterious recessive alleles, and often to developmental abnormalities. Both captive-born and wild-born copperheads and cottonmouths appear to be capable of this form of parthenogenesis.[93]

Reproduction in squamate reptiles is almost exclusively sexual. Males ordinarily have a ZZ pair of sex-determining chromosomes, and females a ZW pair. However, the Colombian Rainbow boa (Epicrates maurus) can also reproduce by facultative parthenogenesis, resulting in production of WW female progeny.[94] The WW females are likely produced by terminal automixis.[citation needed]

Embryonic development

[edit]
Mouse embryo 12 day post fertilization side by side with corn snake embryo 2 days post ovo-positioning[95]

Snake embryonic development initially follows similar steps as any vertebrate embryo. The snake embryo begins as a zygote, undergoes rapid cell division, forms a germinal disc, also called a blastodisc, then undergoes gastrulation, neurulation, and organogenesis.[96] Cell division and proliferation continues until an early snake embryo develops and the typical body shape of a snake can be observed.[96] Multiple features differentiate the embryologic development of snakes from other vertebrates, two significant factors being the elongation of the body and the lack of limb development.[citation needed]

Diagram illustrating differential somite size due to difference in somitogenesis clock oscillation[95]

The elongation in snake body is accompanied by a significant increase in vertebra count (mice have 60 vertebrae, whereas snakes may have over 300).[95] This increase in vertebrae is due to an increase in somites during embryogenesis, leading to an increased number of vertebrae which develop.[95] Somites are formed at the presomitic mesoderm due to a set of oscillatory genes that direct the somitogenesis clock. The snake somitogenesis clock operates at a frequency 4 times that of a mouse (after correction for developmental time), creating more somites, and therefore creating more vertebrae.[95] This difference in clock speed is believed to be caused by differences in Lunatic fringe gene expression, a gene involved in the somitogenesis clock.[97]

There is ample literature focusing on the limb development/lack of development in snake embryos and the gene expression associated with the different stages. In basal snakes, such as the python, embryos in early development exhibit a hind limb bud that develops with some cartilage and a cartilaginous pelvic element, however this degenerates before hatching.[98] This presence of vestigial development suggests that some snakes are still undergoing hind limb reduction before they are eliminated.[99] There is no evidence in basal snakes of forelimb rudiments and no examples of snake forelimb bud initiation in embryo, so little is known regarding the loss of this trait.[99] Recent studies suggest that hind limb reduction could be due to mutations in enhancers for the SSH gene,[99] however other studies suggested that mutations within the Hox Genes or their enhancers could contribute to snake limblessness.[95] Since multiple studies have found evidence suggesting different genes played a role in the loss of limbs in snakes, it is likely that multiple gene mutations had an additive effect leading to limb loss in snakes[100]

Behavior and life history

[edit]
Snake coiled on a stick in Oklahoma. It was brumating in a large pile of wood chips, found by this landscaper after he bulldozed the pile in late autumn 2018.

Winter dormancy

[edit]
A snaked coiled in the cavity of a tree

In regions where winters are too cold for snakes to tolerate while remaining active, local species will enter a period of brumation. Unlike hibernation, in which the dormant mammals are actually asleep, brumating reptiles are awake but inactive. Individual snakes may brumate in burrows, under rock piles, or inside fallen trees, or large numbers of snakes may clump together in hibernacula.[101]

Feeding and diet

[edit]
African egg-eating snake eating an egg
Dolichophis jugularis preying on a sheltopusik
Eastern hognose hooding

All snakes are strictly carnivorous, preying on small animals including lizards, frogs, other snakes, small mammals, birds, eggs, fish, snails, worms, and insects.[26]: 81 [27][102] Snakes cannot bite or tear their food to pieces so must swallow their prey whole. The eating habits of a snake are largely influenced by body size; smaller snakes eat smaller prey. Juvenile pythons might start out feeding on lizards or mice and graduate to small deer or antelope as an adult, for example.[citation needed]

The snake's jaw is a complex structure. Contrary to the popular belief that snakes can dislocate their jaws, they have an extremely flexible lower jaw, the two halves of which are not rigidly attached, and numerous other joints in the skull, which allow the snake to open its mouth wide enough to swallow prey whole, even if it is larger in diameter than the snake itself.[102] For example, the African egg-eating snake has flexible jaws adapted for eating eggs much larger than the diameter of its head.[26]: 81  This snake has no teeth, but does have bony protrusions on the inside edge of its spine, which it uses to break the shell when eating eggs.[26]: 81 

The majority of snakes eat a variety of prey animals, but there is some specialization in certain species. King cobras and the Australian bandy-bandy consume other snakes. Species of the family Pareidae have more teeth on the right side of their mouths than on the left, as they mostly prey on snails and the shells usually spiral clockwise.[26]: 184 [103][104]

Some snakes have a venomous bite, which they use to kill their prey before eating it.[102][105] Other snakes kill their prey by constriction,[102] while some swallow their prey when it is still alive.[26]: 81 [102]

After eating, snakes become dormant to allow the process of digestion to take place;[67] this is an intense activity, especially after consumption of large prey. In species that feed only sporadically, the entire intestine enters a reduced state between meals to conserve energy. The digestive system is then 'up-regulated' to full capacity within 48 hours of prey consumption. Being ectothermic ("cold-blooded"), the surrounding temperature plays an important role in the digestion process. The ideal temperature for snakes to digest food is 30 °C (86 °F). There is a huge amount of metabolic energy involved in a snake's digestion, for example the surface body temperature of the South American rattlesnake (Crotalus durissus) increases by as much as 1.2 °C (2.2 °F) during the digestive process.[106] If a snake is disturbed after having eaten recently, it will often regurgitate its prey to be able to escape the perceived threat. When undisturbed, the digestive process is highly efficient; the snake's digestive enzymes dissolve and absorb everything but the prey's hair (or feathers) and claws, which are excreted along with waste.[citation needed]

Hooding and spitting

[edit]

Hooding (expansion of the neck area) is a visual deterrent, mostly seen in cobras (elapids), and is primarily controlled by rib muscles.[107] Hooding can be accompanied by spitting venom towards the threatening object,[108] and producing a specialized sound; hissing. Studies on captive cobras showed that 13–22% of the body length is raised during hooding.[109]

Locomotion

[edit]

The lack of limbs does not impede the movement of snakes. They have developed several different modes of locomotion to deal with particular environments. Unlike the gaits of limbed animals, which form a continuum, each mode of snake locomotion is discrete and distinct from the others; transitions between modes are abrupt.[110][111]

Lateral undulation

[edit]
Crawling prints of a snake

Lateral undulation is the sole mode of aquatic locomotion, and the most common mode of terrestrial locomotion.[111] In this mode, the body of the snake alternately flexes to the left and right, resulting in a series of rearward-moving "waves".[110] While this movement appears rapid, snakes have rarely been documented moving faster than two body-lengths per second, often much less.[112] This mode of movement has the same net cost of transport (calories burned per meter moved) as running in lizards of the same mass.[113]

Terrestrial lateral undulation is the most common mode of terrestrial locomotion for most snake species.[110] In this mode, the posteriorly moving waves push against contact points in the environment, such as rocks, twigs, irregularities in the soil, etc.[110] Each of these environmental objects, in turn, generates a reaction force directed forward and towards the midline of the snake, resulting in forward thrust while the lateral components cancel out.[114] The speed of this movement depends upon the density of push-points in the environment, with a medium density of about 8[clarification needed] along the snake's length being ideal.[112] The wave speed is precisely the same as the snake speed, and as a result, every point on the snake's body follows the path of the point ahead of it, allowing snakes to move through very dense vegetation and small openings.[114]

When swimming, the waves become larger as they move down the snake's body, and the wave travels backwards faster than the snake moves forwards.[115] Thrust is generated by pushing their body against the water, resulting in the observed slip. In spite of overall similarities, studies show that the pattern of muscle activation is different in aquatic versus terrestrial lateral undulation, which justifies calling them separate modes.[116] All snakes can laterally undulate forward (with backward-moving waves), but only sea snakes have been observed reversing the motion (moving backwards with forward-moving waves).[110]

Sidewinding

[edit]
A neonate sidewinder rattlesnake (Crotalus cerastes) sidewinding

Most often employed by colubroid snakes (colubrids, elapids, and vipers) when the snake must move in an environment that lacks irregularities to push against (rendering lateral undulation impossible), such as a slick mud flat, or a sand dune, sidewinding is a modified form of lateral undulation in which all of the body segments oriented in one direction remain in contact with the ground, while the other segments are lifted up, resulting in a peculiar "rolling" motion.[117][118] The sidewinder moves forward by throwing a loop of itself and then pulling itself up by it. By lowering its head the snake gets leverage, straightening itself out and pressing itself against the ground, it brings itself forward and at an angle that leaves it ready for the next jump. The head and the loop are in effect the two feet upon which the snake walks. The snake's body, appearing roughly perpendicular to its direction, may bewilder the observer, since preconception may lead one to associate snake movement with a head that leads and a body that follows. It appears the sidewinder is going sideways - but precisely where the snake is going, where it wants to go, the head gives clear indication. The snake leaves behind a trail that looks like a series of hooks one after the next. Snakes can move backwards to retreat from an enemy, though they normally do not.[52][page needed] This mode of locomotion overcomes the slippery nature of sand or mud by pushing off with only static portions on the body, thereby minimizing slipping.[117] The static nature of the contact points can be shown from the tracks of a sidewinding snake, which show each belly scale imprint, without any smearing. This mode of locomotion has very low caloric cost, less than 13 of the cost for a lizard to move the same distance.[113] Contrary to popular belief, there is no evidence that sidewinding is associated with the sand being hot.[117]

Concertina

[edit]

When push-points are absent, but there is not enough space to use sidewinding because of lateral constraints, such as in tunnels, snakes rely on concertina locomotion.[110][118] In this mode, the snake braces the posterior portion of its body against the tunnel wall while the front of the snake extends and straightens.[117] The front portion then flexes and forms an anchor point, and the posterior is straightened and pulled forwards. This mode of locomotion is slow and very demanding, up to seven times the cost of laterally undulating over the same distance.[113] This high cost is due to the repeated stops and starts of portions of the body as well as the necessity of using active muscular effort to brace against the tunnel walls.[citation needed]

Arboreal

[edit]
Golden tree snake climbing a flower

The movement of snakes in arboreal habitats has only recently been studied.[119] While on tree branches, snakes use several modes of locomotion depending on species and bark texture.[119] In general, snakes will use a modified form of concertina locomotion on smooth branches, but will laterally undulate if contact points are available.[119] Snakes move faster on small branches and when contact points are present, in contrast to limbed animals, which do better on large branches with little 'clutter'.[119]

Gliding snakes (Chrysopelea) of Southeast Asia launch themselves from branch tips, spreading their ribs and laterally undulating as they glide between trees.[117][120][121] These snakes can perform a controlled glide for hundreds of feet depending upon launch altitude and can even turn in midair.[117][120]

Rectilinear

[edit]

The slowest mode of snake locomotion is rectilinear locomotion, which is also the only one where the snake does not need to bend its body laterally, though it may do so when turning.[122] In this mode, the belly scales are lifted and pulled forward before being placed down and the body pulled over them. Waves of movement and stasis pass posteriorly, resulting in a series of ripples in the skin.[122] The ribs of the snake do not move in this mode of locomotion and this method is most often used by large pythons, boas, and vipers when stalking prey across open ground as the snake's movements are subtle and harder to detect by their prey in this manner.[117]

Interactions with humans

[edit]
Most common symptoms of any kind of snake bite envenomation.[123][124] Furthermore, there is vast variation in symptoms between bites from different types of snakes.[123]

Bite

[edit]
Vipera berus, one fang in glove with a small venom stain, the other still in place

Snakes do not ordinarily prey on humans. Unless startled or injured, most snakes prefer to avoid contact and will not attack humans. With the exception of large constrictors, nonvenomous snakes are not a threat to humans. The bite of a nonvenomous snake is usually harmless; their teeth are not adapted for tearing or inflicting a deep puncture wound, but rather grabbing and holding. Although the possibility of infection and tissue damage is present in the bite of a nonvenomous snake, venomous snakes present far greater hazard to humans.[26]: 209  The World Health Organization (WHO) lists snakebite under the "other neglected conditions" category.[125]

Documented deaths resulting from snake bites are uncommon. Nonfatal bites from venomous snakes may result in the need for amputation of a limb or part thereof. Of the roughly 725 species of venomous snakes worldwide, only 250 are able to kill a human with one bite. Australia averages only one fatal snake bite per year. In India, 250,000 snakebites are recorded in a single year, with as many as 50,000 recorded initial deaths.[126] The WHO estimates that on the order of 100,000 people die each year as a result of snake bites, and around three times as many amputations and other permanent disabilities are caused by snakebites annually.[127]

The health of people is seriously threatened by snakebites, especially in areas where there is a great diversity of snakes and little access to medical care such as the Amazon Rainforest region in South America.[128] Snakebite is classified by the World Health Organization (WHO) as "other neglected conditions".[129] Although there aren't many recorded snakebite deaths, the bites can cause serious complications and permanent impairments.[129] The most successful treatment for snakebites is still antivenom, which is made from snake venom.[129] However, access to antivenom differs greatly by location, with rural areas frequently experiencing difficulties with both cost and availability.[130] Clinical studies, serum preparation, and venom extraction are among the intricate procedures involved in the manufacturing of antivenom.[130] The development of alternative treatments and increased accessibility and affordability of antivenom are essential for reducing the global impact of snake bites on human populations.[131]

Snake charmers

[edit]
The Indian cobra is the most common subject of snake charmings.

In some parts of the world, especially in India, snake charming is a roadside show performed by a charmer. In such a show, the snake charmer carries a basket containing a snake that he seemingly charms by playing tunes with his flutelike musical instrument, to which the snake responds.[132] The snake is in fact responding to the movement of the flute, not the sound it makes, as snakes lack external ears (though they do have internal ears).[132]

The Wildlife Protection Act of 1972 in India technically prohibits snake charming on the grounds of reducing animal cruelty. Other types of snake charmers use a snake and mongoose show, where the two animals have a mock fight; however, this is not very common, as the animals may be seriously injured or killed. Snake charming as a profession is dying out in India because of competition from modern forms of entertainment and environment laws proscribing the practice. Many Indians have never seen snake charming and it is becoming a folktale of the past.[132][133][134][135]

Trapping

[edit]

The Irulas tribe of Andhra Pradesh and Tamil Nadu in India have been hunter-gatherers in the hot, dry plains forests, and have practiced the art of snake catching for generations. They have a vast knowledge of snakes in the field. They generally catch the snakes with the help of a simple stick. Earlier, the Irulas caught thousands of snakes for the snake-skin industry. After the complete ban of the snake-skin industry in India and protection of all snakes under the Indian Wildlife (Protection) Act 1972, they formed the Irula Snake Catcher's Cooperative and switched to catching snakes for removal of venom, releasing them in the wild after four extractions. The venom so collected is used for producing life-saving antivenom, biomedical research and for other medicinal products.[136] The Irulas are also known to eat some of the snakes they catch and are very useful in rat extermination in the villages.[citation needed]

Despite the existence of snake charmers, there have also been professional snake catchers or wranglers. Modern-day snake trapping involves a herpetologist using a long stick with a V-shaped end. Some television show hosts, like Bill Haast, Austin Stevens, Steve Irwin, and Jeff Corwin, prefer to catch them using bare hands.[citation needed]

Consumption

[edit]
Snake meat, in a Taipei restaurant

Consuming snake flesh and related goods is a reflection of many cultures around the world, especially in Asian nations like China, Taiwan, Thailand, Indonesia, Vietnam, and Cambodia. Because of its supposed health benefits and aphrodisiac qualities, snake meat is frequently regarded as a delicacy and ingested.[137] It is customary to drink wine laced with snake blood in an attempt to increase virility and vigor.[137] Traditional Chinese medicine holds that snake wine, a traditional beverage infused with whole snakes, offers medicinal uses.[137] Snake wine's origins are in Chinese culture. However, using snake goods creates moral questions about conservation and animal welfare.[138] It is important to pay attention to and regulate the sustainable harvesting of snakes for human food, particularly in areas where snake populations are in decline as a result of habitat degradation and overexploitation.[138]

Pets

[edit]

In the Western world, some snakes are kept as pets, especially docile species such as the ball python and corn snake. To meet the demand, a captive breeding industry has developed. Snakes bred in captivity are considered preferable to specimens caught in the wild and tend to make better pets.[139] Compared with more traditional types of companion animal, snakes can be very low-maintenance pets; they require minimal space, as most common species do not exceed 5 feet (1.5 m) in length, and can be fed relatively infrequently—usually once every five to fourteen days. Certain snakes have a lifespan of more than 40 years if given proper care.[citation needed]

Symbolism

[edit]
The reverse side of the throne of Pharaoh Tutankhamun with four golden uraeus cobra figures. Gold with lapis lazuli; Valley of the Kings, Thebes (1347–37 BCE).
Snakes composing a bronze kerykeion from the mythical Longanus river in Sicily

In ancient Mesopotamia, Nirah, the messenger god of Ištaran, was represented as a serpent on kudurrus, or boundary stones.[140] Representations of two intertwined serpents are common in Sumerian art and Neo-Sumerian artwork[140] and still appear sporadically on cylinder seals and amulets until as late as the thirteenth century BC.[140] The horned viper (Cerastes cerastes) appears in Kassite and Neo-Assyrian kudurrus[140] and is invoked in Assyrian texts as a magical protective entity.[140] A dragon-like creature with horns, the body and neck of a snake, the forelegs of a lion, and the hind-legs of a bird appears in Mesopotamian art from the Akkadian Period until the Hellenistic Period (323 BC–31 BC).[140] This creature, known in Akkadian as the mušḫuššu, meaning "furious serpent", was used as a symbol for particular deities and also as a general protective emblem.[140] It seems to have originally been the attendant of the Underworld god Ninazu,[140] but later became the attendant to the Hurrian storm-god Tishpak, as well as, later, Ninazu's son Ningishzida, the Babylonian national god Marduk, the scribal god Nabu, and the Assyrian national god Ashur.[140]

In Egyptian history, the snake occupies a primary role with the Nile cobra adorning the crown of the pharaoh in ancient times. It was worshipped as one of the gods and was also used for sinister purposes: murder of an adversary and ritual suicide (Cleopatra).[141] The ouroboros was a well-known ancient Egyptian symbol of a serpent swallowing its own tail.[142] The precursor to the ouroboros was the "Many-Faced",[142] a serpent with five heads, who, according to the Amduat, the oldest surviving Book of the Afterlife, was said to coil around the corpse of the sun god Ra protectively.[142] The earliest surviving depiction of a "true" ouroboros comes from the gilded shrines in the tomb of Tutankhamun.[142] In the early centuries AD, the ouroboros was adopted as a symbol by Gnostic Christians[142] and chapter 136 of the Pistis Sophia, an early Gnostic text, describes "a great dragon whose tail is in its mouth".[142] In medieval alchemy, the ouroboros became a typical western dragon with wings, legs, and a tail.[142]

In the Bible, King Nahash of Ammon, whose name means "Snake", is depicted very negatively, as a particularly cruel and despicable enemy of the ancient Hebrews.[citation needed]

Medusa (1597) by the Italian artist Caravaggio

The ancient Greeks used the Gorgoneion, a depiction of a hideous face with serpents for hair, as an apotropaic symbol to ward off evil.[143] In a Greek myth described by Pseudo-Apollodorus in his Bibliotheca, Medusa was a Gorgon with serpents for hair whose gaze turned all those who looked at her to stone and was slain by the hero Perseus.[144][145][146] In the Roman poet Ovid's Metamorphoses, Medusa is said to have once been a beautiful priestess of Athena, whom Athena turned into a serpent-haired monster after she was raped by the god Poseidon in Athena's temple.[147] In another myth referenced by the Boeotian poet Hesiod and described in detail by Pseudo-Apollodorus, the hero Heracles is said to have slain the Lernaean Hydra,[148][149] a multiple-headed serpent which dwelt in the swamps of Lerna.[148][149]

The legendary account of the foundation of Thebes mentioned a monster snake guarding the spring from which the new settlement was to draw its water. In fighting and killing the snake, the companions of the founder Cadmus all perished—leading to the term "Cadmean victory" (i.e. a victory involving one's own ruin).[150]

Rod of Asclepius, in which the snake, through ecdysis, symbolizes healing

Three medical symbols involving snakes that are still used today are Bowl of Hygieia, symbolizing pharmacy, and the Caduceus and Rod of Asclepius, which are symbols denoting medicine in general.[66]

One of the etymologies proposed for the common female first name Linda is that it might derive from Old German Lindi or Linda, meaning a serpent.[citation needed]

India is often called the land of snakes and is steeped in tradition regarding snakes.[151] Snakes are worshipped as gods even today with many women pouring milk on snake pits (despite snakes' aversion for milk).[151] The cobra is seen on the neck of Shiva and Vishnu is depicted often as sleeping on a seven-headed snake or within the coils of a serpent.[152] There are also several temples in India solely for cobras sometimes called Nagraj (King of Snakes) and it is believed that snakes are symbols of fertility. There is a Hindu festival called Nag Panchami each year on which day snakes are venerated and prayed to. See also Nāga.[153]

The snake is one of the 12 celestial animals of Chinese zodiac, in the Chinese calendar.[154]

Many ancient Peruvian cultures worshipped nature.[155] They emphasized animals and often depicted snakes in their art.[156]

Religion

[edit]
Ballcourt marker from the Postclassic site of Mixco Viejo in Guatemala. This sculpture depicts Kukulkan, jaws agape, with the head of a human warrior emerging from his maw.[157]

Snakes are used in Hinduism as a part of ritual worship.[158] In the annual Nag Panchami festival, participants worship either live cobras or images of Nāgas. Lord Shiva is depicted in most images with a snake coiled around his neck.[159] Puranic literature includes various stories associated with snakes, for example Shesha is said to hold all the planets of the Universe on his hoods and to constantly sing the glories of Vishnu from all his mouths. Other notable snakes in Hinduism are Vasuki, Takshaka, Karkotaka, and Pingala. The term Nāga is used to refer to entities that take the form of large snakes in Hinduism and Buddhism.[160]

Snakes have been widely revered in many cultures, such as in ancient Greece where the serpent was seen as a healer.[161] Asclepius carried a serpent wound around his wand, a symbol seen today on many ambulances.[162] In Judaism, the snake of brass is also a symbol of healing, of one's life being saved from imminent death.[163]

In religious terms, the snake and jaguar were arguably the most important animals in ancient Mesoamerica.[164] "In states of ecstasy, lords dance a serpent dance; great descending snakes adorn and support buildings from Chichen Itza to Tenochtitlan, and the Nahuatl word coatl meaning serpent or twin, forms part of primary deities such as Mixcoatl, Quetzalcoatl, and Coatlicue."[165] In the Maya and Aztec calendars, the fifth day of the week was known as Snake Day.[citation needed]

In some parts of Christianity, the redemptive work of Jesus Christ is compared to saving one's life through beholding the Nehushtan (serpent of brass).[166] Snake handlers use snakes as an integral part of church worship, to demonstrate their faith in divine protection. However, more commonly in Christianity, the serpent has been depicted as a representative of evil and sly plotting, as seen in the description in Genesis of a snake tempting Eve in the Garden of Eden.[167] Saint Patrick is purported to have expelled all snakes from Ireland while converting the country to Christianity in the 5th century, thus explaining the absence of snakes there.[168]

In Christianity and Judaism, the snake makes its infamous appearance in the first book of the Bible when a serpent appears before Adam and Eve and tempts them with the forbidden fruit from the Tree of Knowledge.[167] The snake returns in the Book of Exodus when Moses turns his staff into a snake as a sign of God's power, and later when he makes the Nehushtan, a bronze snake on a pole that when looked at cured the people of bites from the snakes that plagued them in the desert. The serpent makes its final appearance symbolizing Satan in the Book of Revelation: "And he laid hold on the dragon the old serpent, which is the devil and Satan, and bound him for a thousand years."[169]

In Neo-Paganism and Wicca, the snake is seen as a symbol of wisdom and knowledge.[170] Additionally, snakes are sometimes associated with Hecate, the Greek goddess of witchcraft.[171]

Medicine

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Several compounds from snake venoms are being researched as potential treatments or preventatives for pain, cancers, arthritis, stroke, heart disease, hemophilia, and hypertension, as well as to control bleeding (e.g., during surgery).[172][173][174]

See also

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References

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Further reading

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Snakes (suborder Serpentes) are limbless reptiles characterized by their elongated, cylindrical bodies covered in overlapping keratinous scales, which help prevent water loss and aid in locomotion. They belong to the order within the class Reptilia and are classified as tetrapods, despite the absence of limbs, because they evolved from four-limbed ancestors. Ectothermic vertebrates, snakes regulate their body through behavioral adaptations like basking or seeking shade, and they lack external openings, movable eyelids, and limbs, instead relying on a highly flexible for movement via undulating or locomotion. With over 4,000 extant , snakes exhibit remarkable diversity in size, from the thread snake (Tetracheilostoma carlae) at under 10 cm to the ( reticulatus) exceeding 6 m in length. They inhabit virtually every terrestrial and aquatic ecosystem on except , ranging from tropical rainforests and deserts to temperate grasslands and oceans, with adaptations enabling terrestrial, , arboreal, or fully aquatic lifestyles. As carnivorous predators, snakes play a crucial ecological role in controlling populations of , birds, amphibians, and other reptiles, using methods such as to suffocate prey or delivered via specialized fangs in about 600 species. Their sensory systems emphasize chemoreception, with forked tongues transferring scents to the Jacobson's organ for detailed environmental mapping, supplemented by vibration detection and, in pit vipers, infrared-sensing loreal pits for locating warm-blooded prey. Reproduction in snakes involves , with most oviparous—laying leathery, amniotic eggs that develop on land—though approximately half in regions like are viviparous, giving birth to live young. Snakes periodically shed their entire skin, including a transparent over the eyes in place of eyelids, to accommodate growth and remove parasites, with frequency varying by age and . While many snakes are harmless to humans and essential for balance, venomous pose risks through bites, though fatalities are rare with proper medical intervention. Conservation challenges include habitat loss and , affecting nearly two-thirds of globally.

Naming and Classification

Etymology

The English word "snake" originates from Old English snaca, denoting a creeping or crawling creature, which traces back to Proto-Germanic *snakô. This term ultimately derives from the *snegʷʰ-, meaning "to crawl" or "creeping thing," emphasizing the reptile's sinuous movement. Cognates in other include Sanskrit sarpa, referring to a snake or reptile that creeps along the ground, highlighting a shared linguistic focus on locomotion across ancient tongues. In , Greek employed ophis for "snake" or "serpent," a word linked to Proto-Indo-European *h₁ógʷʰis, possibly evoking the creature's alert, watchful through associations with sight, though primarily descriptive of the animal itself. Similarly, Latin used serpens, meaning "snake" or "creeping thing," derived from the verb serpō ("to creep" or "to slither"), directly rooted in Proto-Indo-European *serp-, which conveys the gliding, winding motion characteristic of serpents. Cultural naming in non-Indo-European languages often relies on onomatopoeic elements or physical descriptions. The Chinese term shé (蛇), meaning "snake," is a phono-semantic compound featuring the "insect" or "worm" radical (chóng, 虫) paired with a phonetic component (, 它), descriptively likening the snake's slender, legless form to a worm or elongated insect. In Nahuatl, the language of the Aztecs, coatl signifies "snake" or "serpent," potentially drawing from the creature's bifurcated tongue or dual symbolism in Mesoamerican lore, serving as a descriptive term for its serpentine duality.

Taxonomy

Snakes are classified within the kingdom Animalia, phylum Chordata, class Reptilia, order , and suborder Serpentes. This placement positions them as a distinct subgroup of squamates, which encompass , snakes, and amphisbaenians, totaling over 12,500 as of 2025. The suborder Serpentes is defined by key morphological traits, including an elongated, limbless body; overlapping keratinous scales covering the skin; and an ectothermic metabolism reliant on external heat sources for . These features facilitate their specialized locomotion and predatory lifestyles, distinguishing them from other squamates while adapting them to diverse terrestrial, arboreal, and aquatic environments. Phylogenetically, snakes form a monophyletic nested within , specifically as part of the group, where they are sister to , with this pair sister to Iguania. Early morphological studies debated snake , suggesting possible polyphyletic origins from burrowing , but comprehensive molecular analyses using thousands of genetic loci across hundreds of taxa have robustly confirmed their unity and derivation from lizard ancestors. Genomic datasets further support this positioning, highlighting snakes' evolutionary singularity within squamates through extreme body elongation and dietary specialization. Unlike legless , which represent across multiple squamate lineages, snakes exhibit unique and scale microstructures.

Families

Snakes are classified into approximately 25 extant families, encompassing 4,203 worldwide (as of September 2025). These families are broadly grouped into two infraorders: , which includes the blind snakes and comprises about 500 across five families characterized by lifestyles, reduced eyes, and specialized burrowing adaptations; and , the true snakes, which account for the remaining diversity with a wide array of ecologies from aquatic to arboreal. The classification reflects phylogenetic relationships based on molecular and morphological data, emphasizing monophyletic groups. The , often called worm snakes or blind snakes, are primarily subterranean and exhibit cylindrical bodies, small mouths, and vestigial limbs in some cases. Representative families include Anomalepididae (~18 species), small burrowers with rigid skulls for soil penetration, exemplified by Liotyphlops beui; Gerrhopilidae (~18 species), African and Asian snakes with unique cranial features, such as Gerrhopilus mirus; (~120 species), thread-like snakes with translucent scales, like Leptotyphlops humilis; (~300 species), the most diverse blind snake group with cylindrical forms and scale-covered eyes, including Typhlops vermicularis; and Xenotyphlopidae (1 species), a endemic with primitive traits, Xenotyphlops grandidieri. These families collectively represent less than 15% of snake diversity but highlight early divergences in snake evolution. Within , the family stands out as the largest, comprising over 50% of all snake species (approximately 2,000+ species), mostly non-venomous or mildly venomous with rear fangs, and exhibiting vast morphological and ecological variation from racers to tree snakes. Distinguishing traits include Duvernoy's glands in some for mild and diverse scale patterns; representative species are the (Pantherophis guttatus), a common North American constrictor, and the (Dispholidus typus), an arboreal African rear-fanged species. Other notable Alethinophidian families include (~60 species), robust constrictors without that subdue prey by , such as the (Boa constrictor); and (~40 species), Old World counterparts with similar constricting habits and oviparous reproduction, exemplified by the (Python reticulatus), one of the longest snakes at up to 6 meters. Venomous families dominate in ecological impact, with Viperidae (~340 species) featuring hinged fangs for efficient venom delivery and often heat-sensing pits in pit vipers; key examples are the western diamondback rattlesnake (Crotalus atrox) from the subfamily Crotalinae and the puff adder (Bitis arietans) from Viperinae. Elapidae (~380 species) possess fixed front fangs and potent neurotoxic venom, including terrestrial forms like the king cobra (Ophiophagus hannah) and aquatic sea kraits (Laticauda spp.). Additional families contribute to niche adaptations, such as Acrochordidae (3 species), fully aquatic file snakes with loose, wrinkled skin for gill-like breathing, like Acrochordus javanicus; Uropeltidae (~55 species), short-tailed shieldtail snakes from South Asia specialized for burrowing, represented by Uropeltis phipsonii; and Homalopsidae (~50 species), mangrove-dwelling mud snakes with keeled scales, such as Homalopsis buccata. Lesser-known groups like Aniliidae (2 species), primitive pipe snakes (Anilius scytale), and Tropidophiidae (~34 species), dwarf boas (Tropidophis melanurus), underscore the infraorder's basal diversity.
FamilyApprox. SpeciesDistinguishing TraitsRepresentative Species
Anomalepididae18Small, rigid-skulled burrowersLiotyphlops beui
Gerrhopilidae18Unique skull, fossorialGerrhopilus mirus
120Thread-like, translucentLeptotyphlops humilis
300Cylindrical, scale-covered eyesTyphlops vermicularis
Xenotyphlopidae1Primitive Madagascar formXenotyphlops grandidieri
3Aquatic, wrinkled skinAcrochordus javanicus
Aniliidae2Pipe-like, burrowingAnilius scytale
Anomochilidae3Dwarf pipe snakesAnomochilus leonardi
60Robust constrictorsBoa constrictor
2Round island boasBolyeria multocarinata
Calabariidae1Burrowing constrictorCalabaria reinhardtii
2,000+Diverse, mostly non-venomousPantherophis guttatus
Cylindrophiidae14Asian pipe snakes rufus
380Fixed fangs, neurotoxic naja
50Aquatic mud snakes
315African, often rear-fanged fuliginosus
Loxocemidae1Mexican burrowing python bicolor
Pareatidae33Slug-eaters, arborealPareas carinatus
40Oviparous constrictorsPython reticulatus
34Dwarf boasTropidophis melanurus
55Shield-tailed burrowersUropeltis phipsonii
Viperidae340Hinged fangs, venomousCrotalus atrox
Xenodermatidae9Odd-scaled, terrestrialXenodermus javanicus
Xenophidiidae2Rare odd-scaledXenophidion schaeferi
Xenopeltidae2Iridescent sunbeam snakesXenopeltis unicolor
This table summarizes the approximately 25 families, with species counts reflecting current estimates and traits highlighting primary adaptations.

Legless lizards

Legless lizards are reptiles within the order that have independently evolved limb reduction or complete loss of limbs multiple times, distinct from the snake suborder Serpentes. These lizards belong to various families, such as Anguidae (which includes glass lizards of the genus and slow worms of the genus ) and (flap-footed lizards, primarily in ). Unlike snakes, which form a monophyletic group with specialized limbless morphology, legless lizards represent across more than 20 lizard lineages. Key anatomical distinctions help differentiate legless lizards from snakes and prevent misidentification. Snakes possess fused eyelids forming a transparent and lack external openings, relying instead on bones to detect vibrations; in contrast, legless retain movable eyelids that allow and visible external holes. Legless lizards typically have broader, more lizard-like heads, inflexible jaws unable to dislocate for swallowing large prey, and tails that often comprise a significant portion of their body length—sometimes up to two-thirds—while snakes have narrower heads, highly kinetic skulls, and shorter tails relative to their bodies. Additionally, the tongues of legless lizards are usually notched or rounded rather than deeply forked as in snakes, and their scales lack the broad ventral scutes typical of snakes. Representative examples illustrate these traits and their ecological roles. Glass lizards ( spp.), found in North American grasslands and woodlands, feature extremely fragile tails that fracture easily for defense, earning their name, and they burrow in loose soil much like some snakes. Slow worms ( and relatives), native to European temperate regions, inhabit gardens, meadows, and forests, where they prey on and occasionally small vertebrates, overlapping with snake niches in soil-dwelling and ground foraging. Pygopodids, such as the legless species in genera like Delma and Lialis, occur in Australian arid and coastal habitats, often retaining tiny vestigial hind limb flaps; some, like Lialis burtonis, are snake-like predators of other , sharing predatory and burrowing behaviors with snakes. This morphological and ecological similarity—both groups thriving in terrestrial, , or semi-fossorial environments—frequently leads to confusion, but the retained lizard features in external provide reliable identification markers.

Evolutionary History

Origins and evolution

Snakes are hypothesized to have originated from burrowing ancestors during the period, approximately 128 to 150 million years ago. This evolutionary transition likely occurred on land in the southern supercontinents, where early snakes adapted to subterranean lifestyles, marking their divergence from other squamate reptiles. Key adaptations that defined early snake evolution included the elongation of the body through an increase in vertebral count and reduction in regionalization, enabling efficient burrowing and locomotion without limbs. The progressive loss of external limbs, vestigial in some primitive forms, further streamlined their form for navigating narrow tunnels and reducing drag in soil. Concurrently, the development of highly flexible jaws, characterized by kinetic skulls and loosely connected quadrates, allowed snakes to large prey whole, a trait that distinguished them from their lizard progenitors. A major evolutionary radiation of snakes occurred during the Paleogene period, following the Cretaceous-Paleogene mass extinction event around 66 million years ago, which eliminated non-avian dinosaurs and opened new ecological niches. This burst in diversification led to the proliferation of snake lineages worldwide, with rapid adaptation to varied environments. Subsequent evolutionary milestones included the emergence of aquatic forms, such as sea snakes that colonized marine habitats, and arboreal species, like certain boas and pythons that exploited tree canopies for hunting and evasion. These expansions underscored snakes' versatility, contributing to their current global distribution and over 3,900 extant species.

Fossil record

The fossil record of snakes is notably incomplete, especially for early terrestrial forms, with most preserved specimens originating from marine or lagoonal environments during the era. The earliest definitive snake fossils date to the mid-Cretaceous period, around 100 million years ago, from Cenomanian-age deposits in . Haasiophis terrasantus, described from a nearly complete , retains well-developed hind limbs and pelvic girdle, indicating a transitional morphology between and limbless snakes; these features suggest it was adapted for a semi-aquatic lifestyle. Similarly, Pachyrhachis problematicus, another contemporaneous find from the same region, exhibits hind limb remnants and a long, slender body suited to marine habitats, further supporting an aquatic origin for early snakes. Post-Cretaceous discoveries highlight the diversification of snakes following the end-Cretaceous . In the early , approximately 58–60 million years ago, cerrejonensis from Colombia's Formation represents the largest known prehistoric snake, with estimates of lengths up to 13 meters and weights exceeding 1,100 kilograms based on vertebral fossils; this giant boid underscores the rapid of snakes in tropical environments after the dinosaur . Marine snake fossils, such as those from the Palaeophiidae family in deposits, further illustrate early oceanic adaptations, with elongated bodies and reduced limbs facilitating swimming in ancient seaways. Significant gaps persist in the record of early terrestrial snakes, as land-based specimens are rare compared to aquatic ones, complicating reconstructions of snake evolution on continents. Recent discoveries , , have begun to address this scarcity; for instance, multiple specimens of Najash rionegrina from the early (about 95 million years ago) include well-preserved and hind limbs, providing crucial evidence of terrestrial snake and morphology during a critical period. These finds, including a remarkably intact reported in 2019, fill key voids in the terrestrial record and affirm snakes' presence on land well before the .

Genetic basis of evolution

The genetic basis of snake evolution involves key molecular mechanisms that have shaped their distinctive traits, particularly through alterations in developmental regulation. , which control body axis patterning and limb positioning in vertebrates, exhibit expanded expression domains in snakes, contributing to trunk elongation and limb reduction. In python embryos, for instance, the posterior shift and broadening of Hox expression boundaries suppress limb bud formation while promoting an increased number of vertebral segments, a pattern observed across snake . This regulatory reconfiguration, rather than wholesale gene duplications, underlies the limbless , as evidenced by comparative genomic analyses of snake Hox clusters showing conserved content but modified enhancers and promoters.00674-2) Molecular phylogenetic studies in the 2020s have solidified the of snakes (Serpentes) using integrated mitogenomic and nuclear DNA datasets. Analyses of complete mitochondrial genomes from diverse snake families, combined with thousands of nuclear loci, consistently place snakes as a unified within , nested within the group alongside anguimorph and iguanians . These reconstructions, drawing on de novo genome assemblies from 14 snake across 12 families, resolve deep divergences and confirm that snake-specific traits evolved from a common ancestral approximately 170 million years ago. Such evidence refutes earlier debates on and highlights adaptive radiations driven by genetic innovations in and sensory families.00674-2) Recent advances, including CRISPR-based gene editing experiments conducted in the early , have elucidated the roles of developmental genes like Sonic hedgehog (Shh) and ectodysplasin A (EDA) in snake trait evolution. Mutations in the zone of polarizing activity regulatory sequence (ZRS) enhancer of Shh progressively disabled development across snake lineages, a mechanism validated through functional assays linking regulatory loss to limb absence. Similarly, CRISPR-Cas9 knockout of the EDA gene in corn snakes (Pantherophis guttatus) disrupted dorsal-lateral scale formation while preserving ventral scales, revealing how somite-derived positional cues interact with ectodermal signaling to generate hexagonal scale patterns via reaction-diffusion mechanisms. These studies connect patterning genes to broader evolutionary shifts, including venom gland diversification, where co-option of developmental pathways like Shh influences toxin gene regulation and heterogeneity across species.31310-1)

Distribution and Habitat

Global distribution

Snakes have a near-cosmopolitan distribution, occurring on all continents except , where the cold climate precludes their survival. With 4,203 recognized worldwide as of September 2025, they are absent from only a few isolated regions, such as , , and certain remote islands, due to historical biogeographic barriers. The highest species diversity is concentrated in tropical and subtropical zones, particularly in and the , where warm climates and varied ecosystems support rich assemblages. hosts a large number of snake species, reflecting its expansive tropical rainforests and diverse habitats from to . In the , species are distributed across North, Central, and , with hotspots in countries like and . and its surrounding islands feature fewer species, totaling about 170 terrestrial forms, but include highly endemic groups such as the , a subfamily of true adapted to marine environments in the . The global patterns of snake distribution have been profoundly influenced by geological processes, including that fragmented ancient supercontinents like , leading to vicariance and isolated radiations on southern continents. Fluctuations in sea levels during the Pleistocene further shaped insular distributions by alternately connecting and isolating landmasses, facilitating dispersal or on islands. Human activities have also altered ranges through unintentional introductions, exemplified by the (Boiga irregularis), which was transported to from its native Pacific islands in the mid-20th century via military cargo, resulting in its establishment as an invasive predator.

Habitat preferences

Snakes exhibit a wide array of habitat preferences, ranging from terrestrial environments to highly specialized niches, reflecting their evolutionary adaptations to diverse ecological conditions. In terrestrial settings, many species thrive in arid deserts, where species like the (Crotalus cerastes) have developed unique locomotion patterns, such as , to navigate loose sand efficiently and avoid overheating on hot surfaces. Forest-dwelling snakes, including various pythons such as the (Python regius), prefer humid, vegetated areas like and open woodlands, where they utilize leaf litter and burrows for shelter and ambush hunting. Grassland species often select open areas with scattered cover, allowing for through basking while minimizing exposure to predators. Specialized niches further highlight snakes' adaptability. Aquatic habitats are dominated by (family ), which possess sublingual salt glands to excrete excess salt from ingested seawater, enabling prolonged submersion in marine environments. Arboreal species, such as the (Corallus caninus), feature prehensile tails that allow secure gripping of branches in canopies, facilitating movement and prey capture at height. blind snakes (family ), like the Brahminy blind snake (), are adapted to subterranean life in soil, with reduced eyes and cylindrical bodies suited for burrowing through and nests in loose, organic-rich substrates. Snakes frequently exploit microhabitats for , such as burrows that provide stable temperatures and protection from extremes. For instance, many and retreat into rodent burrows during the day to maintain optimal body temperatures, avoiding lethal heat or cold. Recent studies indicate that is driving shifts, with venomous snakes potentially expanding into new anthropogenic landscapes as temperatures rise, altering microhabitat availability and increasing overlap with human areas by 2050 under moderate warming scenarios. A 2025 analysis in projects range shifts for like the (Naja naja) toward northern regions, despite an overall decline in suitable , prompting concerns for stability and human-snake interactions.

Physical Characteristics

Size and morphology

Snakes exhibit a wide range of body sizes, with most species measuring between 0.5 and 2 meters in total length, though extremes occur among certain taxa. The longest verified captive specimen is a ( reticulatus) named Medusa, reaching 7.67 meters. At the opposite end, the (Tetracheilostoma carlae) represents the smallest species, with adults attaining a maximum length of approximately 10 centimeters. Morphological variations in snakes include distinct head shapes and scale patterns that adapt to diverse ecological niches. Many non-venomous snakes possess a cylindrical head, facilitating streamlined movement through burrows or dense vegetation, while venomous viperids often display a more triangular head due to enlarged temporal musculature and venom glands. Dorsal scales vary between smooth and keeled types; smooth scales provide a glossy surface for rapid gliding over substrates, whereas keeled scales feature a central ridge that imparts a rougher texture, potentially enhancing traction during climbing or locomotion on uneven terrain. Tail length relative to body size also differs, with terrestrial species having shorter tails for balance during undulatory movement, and arboreal forms exhibiting proportionally longer tails that aid in grasping branches or stabilizing during navigation. Most snake species demonstrate , continuing to increase in length throughout their lives without a fixed maximum size, a strongly influenced by prey availability. In environments with abundant , individuals achieve larger sizes due to sustained somatic growth, whereas resource scarcity limits elongation and overall mass accumulation. This plasticity allows snakes to adapt body size to fluctuating ecological conditions, optimizing survival and .

Sensory systems

Snakes possess highly specialized sensory systems adapted to their predatory lifestyle and subterranean or nocturnal habits. Olfaction plays a dominant role in environmental perception, facilitated by the , also known as Jacobson's organ, which detects pheromones and non-volatile chemical cues. This accessory olfactory structure consists of sensory neurons expressing vomeronasal receptors that respond to substrates like prey odors and conspecific signals. Snakes actively sample these cues through tongue flicking, where the bifurcated tongue collects particles from the air or substrate and delivers them to the vomeronasal organ via the mouth's roof, enabling precise chemosensory discrimination over distances. This mechanism is particularly crucial for trail-following and mate location, with the olfactory and vomeronasal systems showing distinct receptor profiles for airborne versus contact chemicals. Vision in snakes varies by species but is generally adapted for low-light conditions rather than acute color discrimination. Most snakes exhibit dichromatic vision, with visual pigments sensitive to short-wavelength (UV-blue) and medium- to long-wavelength light, providing limited color perception compared to diurnal vertebrates. Their eyes feature immovable lids covered by a transparent spectacle, and retinas dominated by rod cells for enhanced sensitivity in dim environments, though this comes at the expense of visual acuity. Certain taxa, such as pit vipers (Crotalinae) and some pythons and boas, possess loreal pit organs—facial depressions containing heat-sensitive membranes—that detect infrared radiation from warm-blooded prey. These pits function as thermal imagers, with nerve endings capable of resolving temperature changes as small as 0.001°C, allowing snakes to superimpose thermal and visual information for target acquisition in complete darkness. Beyond olfaction and vision, snakes rely on mechanoreception for detecting vibrations and limited auditory cues. Substrate-borne vibrations are sensed through the lower jawbones, which connect to the via the , transmitting mechanical signals to hair cells in the for localization of prey or predators. This bone conduction pathway enables sensitivity to low-frequency ground vibrations, often below 1000 Hz, without an external tympanum. Airborne sound perception is minimal, as snakes lack a ossicle chain for pressure detection; instead, head vibrations induced by sound waves provide coarse directional information through the same jaw-to-ear linkage. These tactile and vibrational senses complement chemical and thermal detection, forming an integrated perceptual system suited to ambush foraging.

Integument and molting

The integument of snakes consists primarily of epidermal scales made of keratin, which overlap to form a flexible yet protective barrier against mechanical abrasion, desiccation, and pathogens. These scales, composed of both alpha- and beta-keratins, enable efficient locomotion by reducing friction on the dorsal surface while providing grip through specialized ventral modifications. Snakes lack most skin glands, relying instead on behavioral adaptations for moisture regulation. Color patterns in snake skin, crucial for , arise from the layered arrangement of chromatophores in the : melanophores produce black or brown pigments, xanthophores contribute yellows and reds, and iridophores generate iridescent structural colors through light reflection. These pigment cells allow for diverse mottled, banded, or blotched patterns that blend with habitats, enhancing without dynamic color change. Molting, or , is a periodic renewal process where snakes shed their entire outer skin layer, including the transparent eye caps known as , to accommodate growth and remove parasites. The cycle is hormonally regulated, primarily by that initiate epidermal separation, occurring every 4-6 weeks in juveniles due to rapid growth rates and less frequently (2-4 times annually) in adults. Prior to shedding, the eyes cloud over as the new forms beneath the old, temporarily impairing vision. Certain adaptations enhance function, such as iridescent scales in like the green tree snake, produced by crystals in iridophores for visual signaling or . Ventral scales are enlarged and textured to provide traction during lateral undulation, preventing slippage on substrates by increasing surface .

Skeletal structure

The snake skull is highly kinetic, featuring a specialized that articulates the lower jaw with the cranium via streptostyly, allowing independent movement of the jaw relative to the braincase. This kinetic mechanism, involving over 20 loosely connected bones, enables extreme flexibility during feeding, particularly a wide gape that permits ingestion of prey larger than the head itself. In macrostomatan snakes, the quadrate's posteroventral tilt and lateral displacement of the mandibular condyle further enhance this gape, facilitating the consumption of large, intact prey items. The vertebral column forms the primary skeletal axis in snakes, consisting of 200 to 400 vertebrae that contribute to their elongated body form. These vertebrae are regionalized into specialized segments, including a short cervical region (typically 1-2 vertebrae without ), an extensive dorsal or trunk region with for support, and a caudal region comprising the vertebrae. This hyper-regionalization, with four morphologically distinct precloacal domains (cervical, anterior thoracic, posterior thoracic, and ), allows for differential flexibility and elongation, far exceeding the vertebral count in other squamates. The increased number and modular structure of these vertebrae underpin the snake's limbless locomotion by enabling lateral undulation and other gaits. Limb remnants in snakes reflect their evolutionary history of limb reduction, with vestigial pelvic girdles present in more advanced (derived) taxa but often reduced to internal, non-ossified traces. In contrast, basal snake groups such as boas and pythons retain more prominent vestiges, manifesting externally as paired spurs near the , which are remnants of the pelvic girdle and bones. These structures, including tiny femora and reduced girdle elements, are homologous to those in limbed ancestors and occasionally ossify in certain species.

Internal organs

Snakes exhibit highly modified internal organs adapted to their elongated, limbless body plan, which prioritizes space efficiency and accommodates infrequent but large meals. This results in significant asymmetry and linear arrangement of viscera, with many paired organs reduced or positioned sequentially rather than side-by-side to elongate the body cavity. The digestive system is particularly elongated to facilitate the slow processing of whole prey items. The esophagus features longitudinal folds allowing extreme distension for swallowing large meals, while the stomach expands dramatically during digestion. The small and large intestines are slender and extended, enabling efficient nutrient absorption over time without the need for rapid transit, as snakes often fast for weeks or months between feedings. Associated organs like the liver, which produces bile, and the pancreas, which aids in enzymatic breakdown and blood sugar regulation, are also linearly arranged and can hypertrophy post-feeding to support heightened metabolic demands. Respiratory adaptations reflect the body's , with most snakes possessing a single functional right that is elongated and vascularized for , while the left is typically vestigial, reduced in size, or entirely absent. This tracheal elongation and right-lung dominance evolved to maximize respiratory efficiency within the narrow , with developmental —such as delayed growth of the left bronchial bud—driving the asymmetry across species. The includes a three-chambered heart located approximately one-third of the body length from the head in many , which is notably mobile within the coelomic cavity due to the absence of a diaphragm. This mobility allows the heart to shift posteriorly during as the expands, preventing compression and maintaining flow to vital tissues. Female reproductive organs are bifurcated, featuring paired ovaries and oviducts that converge at the , with the hemiclitores—a paired, erectile clitoral structure—present in the genital region for copulatory functions. This duality mirrors male hemipenes and supports species-specific behaviors, though the hemiclitores vary in size and innervation across taxa. Snakes are uricotelic reptiles, excreting nitrogenous wastes primarily as insoluble uric acid to conserve water. This adaptation involves paired, elongated kidneys positioned posteriorly in the body cavity. The uric acid is combined with fecal material in the cloaca prior to elimination. Snake droppings typically consist of two distinct parts: a dark brown to black, tubular or log-shaped fecal portion containing undigested prey remains (such as hair, bones, or feathers) and a white or chalky uric acid portion (the urine component) that often appears as a cap, streak, or separate deposit. The overall appearance resembles bird droppings but is usually more solid and cylindrical, with size varying according to the snake's size and minimal odor compared to mammal feces. Excretory adaptations in marine species include specialized salt glands, often located sublingually or premaxillary, which secrete hypertonic NaCl solutions to maintain osmotic balance in saltwater environments. These glands, evolved convergently in hydrophiine , enable effective beyond renal capacity, with morphological and biochemical similarities to those in other marine reptiles. Left-sided organs, including kidneys and gonads, are frequently reduced or rudimentary, further emphasizing the body's asymmetric elongation to accommodate locomotion and prey ingestion.

Venom production

Venom in snakes is produced by specialized glands derived from modified salivary glands, known as venom glands in front-fanged species or Duvernoy's glands in rear-fanged colubrids. These glands synthesize a complex mixture of proteins, peptides, enzymes, and other bioactive molecules, with composition varying by species to target specific physiological effects. In elapids, such as cobras and mambas, venom is predominantly neurotoxic, featuring three-finger toxins and phospholipases A₂ that disrupt neuromuscular transmission. Viperid venoms, in contrast, are primarily hemotoxic, rich in metalloproteinases and serine proteinases that induce coagulopathy and tissue damage. Cytotoxic effects, causing local tissue necrosis, arise from phospholipases A₂ and other components across multiple families, including some colubrids. Venom delivery systems are adapted to fang morphology, enabling efficient injection or secretion into prey. Viperids possess solenoglyphous dentition, with long, hollow fangs on a rotatable maxillary that fold against the roof of the mouth when not in use, allowing high-pressure injection through dual orifices during a strike. Elapids exhibit proteroglyphous fangs—short, fixed, and hollow or grooved at the front of the upper jaw—for direct channeling via a bite-and-hold mechanism. In opisthoglyphous colubrids, rear-positioned grooved fangs deliver through a action, relying on low-pressure from Duvernoy's glands, which is less efficient but sufficient for subduing smaller prey. Approximately 15% of the more than 4,000 snake species worldwide are , with around 600 species possessing , while the remainder, including many constrictors like pythons and boas, lack functional venom glands and instead rely on to subdue prey.

Reproduction and Development

Reproductive biology

Snakes display notable in reproductive anatomy, with males typically possessing relatively longer tails than females to accommodate the paired hemipenes and their retractor muscles. This tail length difference is evident across families like and Viperidae, where the male tail-to-snout-vent length ratio often exceeds that of females by 20-30%, facilitating copulation. Courtship in snakes begins with males detecting female trails using their highly developed , which allows them to follow scent cues over considerable distances. In many species, particularly those with intense male-male competition, escalates into ritualized combat, such as coiling, pushing, or neck-biting displays, to establish dominance and access to the female. These behaviors are phylogenetically conserved, with head-raising and downward pushes ancestral in and . Fertilization is internal, occurring when the male everts one into the female's during copulation, which can last from minutes to hours. Females often store for extended periods, enabling delayed fertilization and multiple clutches from a single mating event in some . Approximately 70% of snake are oviparous, laying eggs that develop externally, while the remaining 30% are viviparous or ovoviviparous, giving birth to live young after internal development. Oviparous , such as pythons, typically deposit clutches in concealed sites and may exhibit maternal guarding to protect eggs from predators and maintain optimal temperatures. In contrast, viviparous like vipers nourish embryos via a placenta-like structure, with birth occurring in protected locations. Clutch or sizes generally range from 5 to 20 , varying with female body size and resource availability, though extremes can reach 3 in small colubrids or up to 46 in large pythons. Snake reproduction is predominantly seasonal, synchronized with environmental cues like rising temperatures and increasing day length in spring or early summer, which trigger gonadal development and mating activity. In temperate regions, breeding often follows from brumation, while tropical may align cycles with wet seasons for enhanced .

Facultative parthenogenesis

Facultative parthenogenesis refers to the optional in female snakes that are capable of , allowing isolated individuals to produce without male fertilization. This reproductive strategy was first documented in snakes in 2010 in captive (Boa constrictor), with subsequent reports in wild pit vipers such as copperheads (Agkistrodon contortrix) and cottonmouths () in 2012, and further confirmations in other boid species. The mechanism involves automixis, a process in which unfertilized ova undergo and subsequent fusion of polar bodies or to restore diploidy, leading to the development of embryos that are genetically identical to the mother at homozygous loci and produce exclusively female offspring. This form of contrasts with obligate parthenogenesis by being facultative, triggered primarily in the absence of males, and has been genetically validated through DNA analysis showing no paternal contribution in the progeny. Documented instances include wild cottonmouth females captured in in 2012, which gave birth to litters confirmed as parthenogenetic via , demonstrating the phenomenon's occurrence in natural populations. In captive settings, a female (Eunectes murinus) isolated for over six years produced a litter of 19 neonates in 2017, with DNA evidence verifying all-female, parthenogenetic origins and low heterozygosity consistent with automixis. More recently, in 2024, the first case was documented in a captive (Chilabothrus subflavus). These cases highlight potential implications for invasive snake populations, where facultative parthenogenesis could enable isolated females to initiate self-sustaining colonies, as suggested by observations in introduced boa populations in regions like .

Embryonic development

Snake embryonic development varies between oviparous and viviparous species, but both exhibit meroblastic cleavage due to the large reserves in their eggs. In oviparous snakes, such as colubrids and pythons, fertilization occurs internally, and eggs are laid after initial cleavage stages, with the consisting of a blastodisc atop the mass. Development proceeds through , where cells migrate to form the three germ layers, followed by , during which major organs like the heart, , and somites form sequentially. Extraembryonic membranes, including the for protection, for gas exchange, for waste storage, and for nutrient absorption, envelop the early in development. Incubation periods for oviparous snake eggs typically range from 40 to 80 days, depending on and environmental , with optimal ranges around 28–32°C for many temperate . Temperature influences developmental rate but is determined genetically in snakes via the ZW chromosomal system. During mid-to-late stages, the absorbs yolk through the vasculature, converting it into nutrients and reducing the yolk mass significantly by hatching; in like the , the transforms into a vascularized tissue that facilitates this process. In viviparous snakes, such as vipers and some boas, embryos develop internally within the oviduct, retaining eggshells initially before evolving placental-like structures for nutrient transfer. Early stages mirror oviparity with cleavage and organogenesis, but the yolk sac and chorioallantoic placenta enable maternal provisioning of water, gases, and ions like calcium, supplementing yolk reserves; for instance, in the water snake Nerodia, placental calcium uptake supports skeletal development. Gestation lasts 3–6 months, with embryos becoming independent near term as yolk absorption completes. Hatching in oviparous involves the using a temporary (caruncle), a sharp, keratinized structure on the rostrum, to slit the in a circular fashion, often starting at the weakened seam. The is shed shortly after emergence, and the may absorb remaining via the external , which is internalized within hours. Viviparous young are born live, emerging from a thin ruptured similarly, without an in some cases. Most snake or neonates are precocial, immediately capable of independent locomotion, feeding, and , though they remain vulnerable to predation. In cases of facultative , embryonic development follows similar stages but originates from unfertilized eggs.

Behavior and Ecology

Dormancy patterns

Snakes in temperate and cold climates undergo brumation, a form of analogous to in mammals but adapted for ectothermic reptiles, during winter months to survive low temperatures. This involves a pronounced reduction in metabolic activity, where rates can decline to 20–30% of normal resting levels through or active metabolic depression, enabling snakes to endure extended periods without feeding by relying on pre-stored . To mitigate loss, many , such as garter snakes and rattlesnakes, cluster communally in underground dens or hibernacula, which provide thermal buffering and protection from freezing conditions; these sites can house hundreds of individuals, with body temperatures stabilizing just above lethal minima. In contrast, snakes inhabiting arid and regions practice during the hottest, driest summer periods to avoid and extreme heat. Species like the (Crotalus atrox) in the burrow into soil, holes, or rocky crevices, forming loose aggregations to minimize loss and maintain lower body temperatures. This similarly suppresses metabolic processes, conserving limited resources until conditions improve with seasonal rains. Dormancy in snakes is primarily triggered by environmental temperatures falling below 10°C for brumation or exceeding 40°C combined with for , prompting physiological shifts such as enhanced and fat accumulation in liver and adipose tissues prior to onset. These reserves, including triacylglycerols and , fuel and basic functions during inactivity, with aiding in lipid breakdown efficiency. Habitat features like rocky outcrops or burrows influence , though patterns remain fundamentally driven by thermal extremes.

Feeding habits

Snakes are carnivores, relying exclusively on animal prey for sustenance throughout their lives. Their diet encompasses a wide spectrum, including mammals, birds, reptiles, amphibians, eggs, and such as and , with prey size often scaled to the snake's body length. For instance, many colubrid snakes consume small , frogs, and birds, while aquatic species like target and eels. A notable dietary specialization is , the consumption of other snakes, observed in kingsnakes (genus Lampropeltis), which subdue venomous prey through and immunity to certain snake venoms. Predatory strategies in snakes vary by species and habitat, broadly dividing into ambush and active pursuit tactics. Ambush predators, such as vipers (family Viperidae), remain motionless for extended periods, relying on to strike passing prey with rapid precision. In contrast, active pursuers like racer snakes (genus Coluber) actively chase or stalk prey over distances, using speed and agility in open environments. Once captured, prey is subdued either through , where non-venomous species like pythons (family ) coil around the victim to suffocate it, or , where venomous snakes inject toxins to immobilize and begin predigestion. These methods ensure efficient capture, with constriction typically taking minutes to hours depending on prey size. Snakes consume prey whole through unhinging their mandibles, allowing the mouth to expand dramatically via elastic ligaments. Swallowing begins at the head, progressing posteriorly with rhythmic muscular contractions, and can take from minutes to hours for large meals. Sensory cues, such as chemical detection via the and Jacobson’s organ, play a key role in locating and identifying prey during . Digestion in snakes is a slow, energy-efficient process adapted to infrequent large meals. Gastric enzymes and acids break down proteins, fats, and bones over 3 to 20 days, depending on prey size and environmental temperature, with higher temperatures accelerating the rate. The process involves sequential stages: initial in the , absorption in the intestines, and elimination of indigestible remains like or scales as castings. Under or stress, snakes may regurgitate undigested prey to lighten their body for escape, a that conserves energy by allowing re-consumption later.

Defensive mechanisms

Snakes employ a variety of non-venomous defensive mechanisms to deter predators, including behavioral bluffing, chemical secretions, and strategies for evasion through or feigned vulnerability. These adaptations allow snakes to avoid confrontation without relying on physical , enhancing survival in diverse habitats. Bluffing behaviors serve to intimidate threats by mimicking more dangerous species or exaggerating the snake's size and ferocity. For instance, cobras (genus ) expand loose skin folds in the neck region to form a hood, a posture that signals warning and evokes heightened in predators, including mammals, more effectively than neutral displays in other snakes. Similarly, non-rattlesnake species like gopher snakes () coil their bodies and rapidly vibrate their tails against substrates, producing a buzzing sound that closely mimics the rattle of venomous rattlesnakes, deterring potential attackers such as or mammals. Hognose snakes (Heterodon spp.), such as the eastern hognose (H. platirhinos), further exemplify bluffing by flattening their necks to resemble a cobra's hood, hissing loudly, and performing open-mouthed bluff strikes without contact, creating the illusion of a more aggressive threat. Chemical defenses provide an additional layer of repulsion, often released from specialized glands to exploit predators' aversion to foul odors or irritants. Many snakes, including garter snakes (Thamnophis spp.) and hognose snakes, secrete a pungent from paired anal glands near the when handled or threatened, which repels and other small predators through contact and repellency; this secretion, rich in carboxylic acids, can cause or death in and deter larger vertebrates by its acrid smell. In a more dramatic example, the European grass snake (Natrix natrix) can engage in , voluntarily rupturing ocular blood vessels to eject blood from the eyes, , and nostrils during thanatosis; this rare , often combined with foul cloacal secretions, aims to disgust or confuse predators, though it is infrequently observed. Camouflage and escape tactics emphasize avoidance over confrontation, leveraging visual and passive responses to minimize detection or pursuit. Snake species exhibit dorsal patterns—such as blotches, bands, or speckling—that provide background matching and , allowing them to blend seamlessly with leaf litter, rocks, or soil; for example, irregularly banded or blotched patterns in many colubrids enhance against visual predators by breaking up the body's outline. When camouflage fails, some snakes resort to rapid evasion or thanatosis ( feigning), adopting a limp, upside-down posture with tongue protrusion and open mouth to simulate a deceased carcass; hognose snakes frequently display this behavior after initial bluffing, while grass snakes (Natrix natrix) use it in response to handling, reducing handling time by generalist predators like birds. These mechanisms collectively prioritize deterrence and escape, underscoring the evolutionary emphasis on behavioral versatility in snake antipredator strategies.

Locomotion strategies

Snakes employ a variety of adapted to diverse substrates, relying on their flexible vertebral column and specialized musculature to generate propulsion without limbs. These modes include lateral undulation, , , rectilinear, and , each characterized by distinct patterns of body bending and substrate interaction. Lateral undulation, the most common mode, involves the propagation of S-shaped waves from the head to the tail, with the body pushing against irregularities in the substrate to advance. This utilizes unilateral activation of epaxial muscles, such as the , dorsi, and , alternating sides to create lateral bends that slide across the ground or water. For instance, water snakes like Nerodia fasciata exhibit increasing wave amplitude and posteriorly in aquatic environments, while terrestrial synchronize wave speed with forward for . Aquatic forms show phase shifts in muscle activation compared to terrestrial ones, highlighting biomechanical adaptations. Sidewinding, employed by certain desert-dwelling , features the formation of lifted body loops that contact the substrate at static points, minimizing friction on loose sands. The snake arches its back bilaterally using muscles while alternating unilateral contractions of the dorsi and to propagate diagonal tracks oblique to the direction of travel. This mode, observed in vipers such as the sidewinder rattlesnake (), combines vertical and lateral waves with a phase offset, resulting in a lower energetic than lateral undulation on granular substrates. Approximately 12 viper utilize this strategy, which lifts sections of the body forward between contact points. Concertina locomotion resembles an , with alternating static anchoring regions and sliding sections that extend and the body length. Epaxial muscles generate convolutions, while ventral flexion or lateral pressure provides grip, varying by context such as tunnels or branches. This mode is used by a wide range of snakes, including the (Python reticulatus) and (Boa constrictor), and is kinematically diverse but metabolically expensive, often requiring up to five times the normal gripping force. It allows navigation through confined spaces by bracing against surfaces. Rectilinear locomotion enables straight-ahead crawling without vertebral bending, achieved through cyclic movement of the ventral skin relative to the stationary . Costocutaneous superior and inferior muscles lift and retract the skin, with the interscutalis modulating stiffness, while belly scales propel the body forward using sequential rib extension. This slow, stealthy mode is characteristic of large boid snakes like the and is limited to forward motion due to immobile skeletal elements. Arboreal locomotion in tree-dwelling snakes adapts these modes for narrow, cluttered branches, often incorporating prehensile tails for looping and anchoring to generate propulsive forces. Species such as the brown treesnake (Boiga irregularis) use lateral undulation with to reduce slipping or with helical wrapping and ventral flexion for grip on cylinders, preventing sagging on uneven supports. Prehensile tails, evolved convergently in many arboreal lineages, anchor to branches during cantilevering or maneuvers, as seen in paradise tree snakes (Chrysopelea spp.), which undulate to control aerial descent. This strategy balances the body on small perches, with performance influenced by branch diameter.

Social interactions

Snakes are predominantly solitary animals, spending much of their active lives independently foraging and avoiding conspecifics outside of breeding periods. However, exceptions occur in certain species, such as garter snakes (Thamnophis spp.), which engage in communal hibernation, or brumation, in large dens known as hibernacula, where thousands may aggregate during winter to share warmth and reduce exposure to predators. These aggregations facilitate post-hibernation mating in groups, with social networks showing sex- and age-based patterns, including female-centric communities that strengthen with maturity. Similar communal behaviors extend to oviposition in some species, where females gather at shared sites for egg-laying, though such interactions remain limited to specific seasonal contexts. Communication among snakes primarily relies on chemical cues, particularly pheromones, which play a crucial role in interactions. Female garter snakes release sex pheromones from their skin to attract males over long distances, guiding them to potential mates through tongue-flicking and vomeronasal detection. Airborne pheromones from copulating pairs can also signal recent to approaching males, inhibiting further attempts to conserve energy, as demonstrated in red-sided garter snakes (Thamnophis sirtalis parietalis). Tactile communication features prominently in male-male interactions during breeding seasons, where rivals engage in ritual combat to establish dominance for access to females. These encounters involve entwining bodies, twisting, rolling, and topping maneuvers, where one male attempts to force the opponent's head to the ground using physical pressure rather than biting, as observed in species like coral snakes (*) and vipers. Although rare, some snakes exhibit social behaviors beyond basic aggregation, including limited parental care and kin-based associations. In pythons, particularly the southern African python (Python natalensis), females provide maternal care by brooding eggs through coiling to regulate temperature and humidity, and extending protection to neonates for up to two weeks post-hatching by allowing them to rest within their coils at night. Rattlesnakes (Crotalus spp.) show communal care, with females sometimes allomothering—caring for unrelated young—while neonates trail maternal scents and aggregate with kin, suggesting recognition through chemical cues. Recent studies, including olfactory experiments in 2024, have further evidenced kin and self-recognition via scents in garter snakes and rattlesnakes, where individuals prefer familiar or related odors, indicating subtle social discrimination.

Human Interactions

Bites and treatment

Snakebites affect millions annually, with the estimating approximately 5.4 million incidents worldwide each year, resulting in 1.8 to 2.7 million cases of and 81,410 to 137,880 deaths. These fatalities occur predominantly in and , where access to treatment is limited, and are primarily caused by bites from viperid (vipers and pit vipers) and elapid (cobras, mambas, and sea snakes) species. In these regions, agricultural workers and children are disproportionately impacted due to encounters in rural areas. Symptoms of snakebites vary based on the species and whether occurs, with local effects including , swelling, and ecchymosis at the bite site, potentially progressing to blistering or in viper bites. Systemic manifestations can range from neurotoxic effects, such as ptosis, , , and respiratory in elapid envenomations, to hemotoxic complications like , hemorrhage, and shock from viper s. Notably, dry bites—where no venom is injected—account for about 50% of cases from venomous snakes, presenting only minor local trauma without systemic involvement, though monitoring is essential to rule out delayed envenomation. Treatment prioritizes rapid medical intervention, with as the cornerstone therapy; polyvalent antivenoms target multiple species common to a region, while monospecific versions address single species for precise neutralization when identified. For neurotoxic bites without significant local swelling, the pressure immobilization technique—applying a firm to immobilize the limb—can slow spread until administration. The updated its guidelines in 2023, emphasizing early use, improved diagnostics like the 20-minute clotting test, and regional protocols to enhance outcomes in high-burden areas. Supportive care, including wound management and respiratory support, is crucial alongside to mitigate complications.

Cultural and recreational uses

is a traditional practiced primarily in and , including , where performers coax snakes, often cobras, to "dance" to the sound of a flute-like instrument such as the in . In , the ( ) is a favored species, kept in wicker baskets and encouraged to rear up in a defensive posture that mimics dancing, though the snakes respond more to the charmer's movements than the music. The ( haje) is similarly used in , where charmers provoke the snakes into striking poses while avoiding their slow attacks. These snakes are typically defanged or undergo venomoid surgery to reduce risk to the performer, a practice common in Indian traditions despite legal restrictions. The form has ancient roots but is declining in due to a 1972 wildlife protection law banning snake possession and performances. Snakes are consumed as a in various cultures, particularly in , , and , where the is valued for its high protein and low fat content, often prepared in soups or grilled dishes. , an alcoholic infusion made by steeping whole snakes—commonly cobras or vipers—in or spirits, is a traditional remedy and beverage believed to have medicinal properties, popular in and southern . Commercial snake farming supports this demand, with thousands of farms across producing tens of millions of snakes annually for , skins, and other products; for instance, recent reports indicate Chinese farms process around 14.5 million snakes per year in regions like Zisiqiao village. These operations, primarily involving pythons and cobras, emphasize , as snakes require minimal feed and water compared to like pigs or chickens. Snakes, especially exotic species like the (Python regius), are popular as pets worldwide, with hundreds of thousands traded annually from African exporters such as , , and to markets in the United States and . Listed under Appendix II since 1977, ball pythons are bred in captivity or ranched to ensure non-detrimental trade, though illegal wild captures persist, prompting recommendations for better monitoring and alternatives. In invasive control efforts, public hunts target non-native species; 's annual Python Challenge, organized by the Florida Fish and Wildlife Conservation Commission and partners, engages participants to remove Burmese pythons (Python bivittatus) from the , with 223 removed in 2021 alone as part of broader removal programs that have eliminated more than 15,000 since 2000. These initiatives, including the Water Management District's Python Elimination Program, use contractors and detection tools to curb ecological damage from invasives.

Conservation and threats

Snakes face significant conservation challenges, with loss being a primary threat. Agricultural expansion, , and have degraded essential habitats, particularly forests, where approximately 30% of species, including many snakes, are at risk of . This destruction disproportionately affects forest-dwelling snakes, which comprise over half of species in such environments and experience higher risks compared to those in arid areas. Human persecution exacerbates these pressures, driven by fear and cultural misconceptions, leading to widespread killing of snakes encountered in human-dominated landscapes. In regions like and , ophidiophobia and retaliatory actions contribute to population declines, with studies showing that negative attitudes reduce tolerance and increase direct mortality. The international further threatens species, with demand for exotic pets fueling illegal collection; for instance, large constrictor snakes like Burmese pythons have been subject to U.S. Fish and Wildlife Service restrictions as injurious species, and 2025 state-level measures in places like aim to curb trafficking of reptiles. According to the , about 20% of assessed snake species are threatened with extinction, a figure aligned with the broader 21.1% for reptiles overall. Hotspots of vulnerability include northern and the northern Amazon ( region), where is high but intensifies risks. also pose localized threats; in Florida's , introduced Burmese pythons have decimated native populations, indirectly impacting snake communities through altered food webs and competition. Conservation efforts focus on mitigating these threats through protected areas, which cover many snake habitats but require stronger enforcement to address ongoing degradation. Anti-poaching initiatives and programs aim to reduce by promoting tolerance and reducing illegal , with organizations like the IUCN Viper Specialist Group advocating for species-specific protections. and reintroduction programs have shown promise; for example, in 2025, 42 eastern indigo snakes were released into preserves as part of recovery efforts for this . Recent advancements in conservation include enhanced monitoring and reduction in Australian fisheries, contributing to population stabilization in coastal waters.

Symbolic and medical significance

Snakes have held profound symbolic meanings across cultures, often embodying themes of renewal, temptation, and healing due to their biological traits like molting and potent . In ancient , the shedding of a snake's skin symbolized rebirth and eternal life, a concept tied to the , the rearing cobra depicted on pharaohs' crowns as a protective emblem of divine authority and sovereignty. In the Abrahamic tradition, particularly in the , the serpent in the represents temptation and deception, luring to eat the forbidden fruit and introducing into the world, which has fostered a lasting association of snakes with and cautionary peril. Conversely, in , the single snake coiled around a staff, known as the , signifies healing and medicine, derived from the god Asclepius's attribute and linked to the snake's regenerative molting; this symbol is widely used in modern healthcare, distinct from the two-snake associated with Hermes and commerce. In religious contexts, snakes occupy dual roles as sacred guardians and objects of fear. In Hinduism, Nagas are semi-divine serpent beings revered as protectors of water sources, treasures, and the underworld, embodying fertility and cosmic balance; they are central to myths like the churning of the ocean, where the Naga king Vasuki serves as the rope. This veneration culminates in festivals such as Nag Panchami, observed on the fifth day of the bright half of Shravana month, where devotees offer milk to snake idols or live cobras to honor these deities and seek protection from snakebites and misfortunes. In contrast, Abrahamic faiths—Judaism, Christianity, and Islam—generally portray snakes with apprehension, stemming from the Genesis narrative where the serpent's cunning leads to humanity's fall; this biblical motif has influenced cultural fears, viewing snakes as embodiments of malice or satanic temptation, though some texts also depict them as instruments of divine judgment, such as the bronze serpent Moses raises for healing. Medically, snake venom has proven a rich source for pharmaceutical innovation, transforming a once-feared into life-saving drugs. In the 1970s, researchers isolated bradykinin-potentiating peptides from the venom of the Brazilian Bothrops jararaca, leading to the development of , the first () inhibitor approved in 1981 for treating and by mimicking the venom's ability to lower . Ongoing research into components, including peptides from species like the that target pain pathways more effectively than opioids, continues to explore potential for non-addictive painkillers in managing chronic conditions such as and neuropathy; as of 2025, advancements include novel antivenoms using human antibodies effective against multiple African species, including mambas.

References

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