Snake
Snake
Snake
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This article is about the reptile. For other uses, see Snake (disambiguation).
Snakes
Temporal range:
Late Cretaceous – Present,[1] 94–0 Ma
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Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
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Class: Reptilia
Order: Squamata
Clade: Ophidia
Suborder: Serpentes
Linnaeus, 1758
Infraorders
• Alethinophidia Nopcsa, 1923
• Scolecophidia Cope, 1864
Etymology
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'.
Evolution
A phylogenetic overview of modern snakes.
Note: the tree only indicates relationships, not evolutionary branching times.[14]
Scolecophidia
Alethinophidia
Leptotyphlopidae
Anomalepididae
Typhlopidae
Amerophidia
Afrophidia
Anilius
Tropidophiidae
Uropeltoidea
Macrostomata
Uropeltidae
Anomochilus
Cylindrophis
Pythonoidea
Caenophidia
Booidea
Pythonidae
Xenopeltis
Loxocemus
Acrochordidae
Xenodermidae
Pareidae
Viperidae
Homalopsidae
Colubridae
Cyclocoridae
Buhoma
Elapidae
Pseudaspididae
Prosymnidae
Psammophiidae
Atractaspididae
Pseudoxyrhophiida
e
Lamprophiidae
Boidae
Erycinae
Calabaria
Ungaliophiinae
Sanzinia
Candoia
The fossil record of snakes is relatively poor because snake skeletons are
typically small and fragile making fossilization uncommon. Fossils readily
identi able as snakes (though often retaining hind limbs) rst appear in the
fossil record during the Cretaceous period.[15] 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,[1] dated to between 112 and 94 million years old.[16]
Based on comparative anatomy, there is consensus that snakes descended
from lizards.[17]: 11 [18] 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.[17]: 11 [19] 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 modi ed in some
aquatic and tree-dwelling species.
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.[20] 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 rst
appearances of vipers and elapids in North America and the signi cant
diversi cation of Colubridae (including the origin of many modern genera
such as Nerodia, Lampropeltis, Pituophis, and Pantherophis).[20]
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Fossils
There is fossil evidence to suggest that snakes may have evolved from
burrowing lizards,[21] during the Cretaceous Period.[22] An early fossil snake
relative, Najash rionegrina, was a two-legged burrowing animal with a
sacrum, and was fully terrestrial.[23] One extant analog of these putative
ancestors is the earless monitor Lanthanotus of Borneo (though it also is
semiaquatic).[24] Subterranean species evolved bodies streamlined for
burrowing, and eventually lost their limbs.[24] According to this hypothesis,
features such as the transparent, fused eyelids (brille) and loss of external
ears evolved to cope with fossorial dif culties, such as scratched corneas and
dirt in the ears.[22][24] 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.[19]
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.[25] 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.[26][27] 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.[28]
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.[18] 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.
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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.[29][30]
•
•
Tetrapodophis
•
Eupodophis descouensi
•
Eupodophis descouensi
•
Eupodophis descouensi hind leg
Distribution
Taxonomy
See also: List of snake genera
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.[39]
The two infraorders of Serpentes are: Alethinophidia and Scolecophidia.[39]
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.[40] While not extant today,
the Madtsoiidae, a family of giant, primitive, python-like snakes, was around
until 50,000 years ago in Australia, represented by genera such as Wonambi.
There are numerous debates in the systematics within the group. For
instance, many sources classify Boidae and Pythonidae as one family, while
some keep the Elapidae and Hydrophiidae (sea snakes) separate for
practical reasons despite their extremely close relation.
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.[14]
Families
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Legless lizards
Main article: Legless lizard
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 super cially look similar to snakes. These include
the slowworm and glass snake.
Other serpentine tetrapods that are unrelated to snakes include caecilians
(amphibians), amphisbaenians (near-lizard squamates), and the extinct
aistopods (amphibians).
Biology
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An adult Barbados threadsnake, Leptotyphlops carlae, on an American quarter dollar
Size
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).[44]
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.[45]
Perception
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
The underside of a snake is very sensitive to vibration, allowing the snake to
detect approaching animals by sensing faint vibrations in the ground.[46]
Despite the lack of outer ears, they are also able to detect airborne sounds.[47]
Snake vision varies greatly between species. Some have keen eyesight and
others are only able to distinguish light from dark, but the important trend is
that a snake's visual perception is adequate enough to track movements.[48]
Generally, vision is best in tree-dwelling snakes and weakest in burrowing
snakes. Some have binocular vision, where both eyes are capable of
focusing on the same point, an example of this being the Asian vine snake.
Most snakes focus by moving the lens back and forth in relation to the retina.
Diurnal snakes have round pupils and many nocturnal snakes have slit pupils.
Most species possess three visual pigments and are probably able to see two
primary colors in daylight. The annulated sea snake and the genus Helicops
appears to have regained much of their color vision as an adaption to the
marine environment they live in.[49][50] It has been concluded that the last
common ancestors of all snakes had UV-sensitive vision, but most snakes
that depend on their eyesight to hunt in daylight have evolved lenses that act
like sunglasses for ltering out the UV-light, which probably also sharpens
their vision by improving the contrast.[51][52]
Skin
Main article: Snake scale
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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.
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.[53]
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.[54]
Snakes have a wide diversity of skin coloration patterns which are often
related to behavior, such as the tendency to have to ee 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.[55]
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.
Molting
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.
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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 skull consists of a solid and complete neurocranium, to which many of
the other bones are only loosely attached, particularly the highly mobile jaw
bones, which facilitate manipulation and ingestion of large prey items. The left
and right sides of the lower jaw are joined only by a exible ligament at the
anterior tips, allowing them to separate widely, and the posterior end of the
lower jaw bones articulate with a quadrate bone, allowing further mobility. The
mandible and quadrate bones can pick up ground-borne vibrations;[61]
because the sides of the lower jaw can move independently of one another, a
snake resting its jaw on a surface has sensitive 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—for receiving vibrations from the air.[62][63]
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.
Caudal autotomy (self-amputation of the tail), a feature found in some lizards,
is absent in most snakes.[64] 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 prede ned fracture plane present on a vertebra.[65][66]
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.
Snakes are polyphyodonts with teeth that are continuously replaced.[67]
Internal organs
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Anatomy of a snake. le 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.[68] Internally, the ventricle is divided
into three interconnected cavities: the cavum arteriosum, the cavum
pulmonale, and the cavum venosum.[69] 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.[70]
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 lters the blood. The thymus,
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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.[71]
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.[71] 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.[71] This 'saccular lung' is used for hydrostatic purposes to adjust
buoyancy in some aquatic snakes and its function remains unknown in
terrestrial species.[71] Many organs that are paired, such as kidneys or
reproductive organs, are staggered within the body, one located ahead of the
other.[71]
Snakes have no lymph nodes.[71]
Venom
See also: Snake venom, Venomous snake, and § Bite
Innocuous milk snakes are often mistaken for coral snakes whose venom is deadly to
humans.
Cobras, vipers, and closely related species use venom to immobilize, injure,
or kill their prey. The venom is modi ed saliva, delivered through fangs.[17][72]: 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-
speci c, and their role in self-defense is secondary.[17][72]: 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.[17][72]: 209
Certain birds, mammals, and other snakes (such as kingsnakes) that prey on
venomous snakes have developed resistance and even immunity to certain
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venoms.[17]: 243 Venomous snakes include three families of snakes, and do not
constitute a formal taxonomic classi cation group.
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.[73] 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).[74]
Snake venoms are complex mixtures of proteins,[72] and are stored in venom
glands at the back of the head.[74] In all venomous snakes, these glands open
through ducts into grooved or hollow teeth in the upper jaw.[17]: 243 [73] 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.[73][72] Almost all snake venom contains hyaluronidase, an
enzyme that ensures rapid diffusion of the venom.[17]: 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.[72][73]
Some snakes that use neurotoxins (such as the mangrove snake) have fangs
in the back of their mouths, with the fangs curled backwards.[75] This makes it
dif cult both for the snake to use its venom and for scientists to milk them.[73]
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.[17]: 242
It has been suggested that all snakes may be venomous to a certain degree,
with harmless snakes having weak venom and no fangs.[76] 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.
Venomous snakes are classi ed in two taxonomic families:
• Elapids – cobras including king cobras, kraits, mambas, Australian
copperheads, sea snakes, and coral snakes.[75]
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• Viperids – vipers, rattlesnakes, copperheads/cottonmouths, and
bushmasters.[75]
There is a third family containing the opistoglyphous (rear-fanged) snakes (as
well as the majority of other snake species):
• Colubrids – boomslangs, tree snakes, vine snakes, cat snakes,
although not all colubrids are venomous.[17]: 209 [75]
Reproduction
See also: Sexual selection in scaled reptiles
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.[77] The hemipenes
are often grooved, hooked, or spined—designed to grip the walls of the
female's cloaca.[78][77] The clitoris of the female snake consists of two
structures located between the cloaca and the scent glands.[79]
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.[77] Most pythons coil around their
egg-clutches and remain with them until they hatch.[80] 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.[80]
Some species of snake are ovoviviparous and retain the eggs within their
bodies until they are almost ready to hatch.[81][82] 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.[81][82] Retention of eggs and live birth are most often associated with
colder environments.[77][82]
Mouse embryo 12 day post fertilization side by side with Corn Snake embryo 2 days
post ovo-positioning.[87]
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.[88] Cell division and proliferation continues
until an early snake embryo develops and the typical body shape of a snake
can be observed.[88] Multiple features differentiate the embryologic
development of snakes from other vertebrates, two signi cant factors being
the elongation of the body and the lack of limb development.
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.[87] This difference in clock speed is believed to be caused by
differences in Lunatic fringe gene expression, a gene involved in the
somitogenesis clock.[89]
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.[90]
This presence of vestigial development suggests that some snakes are still
undergoing hind limb reduction before they are eliminated.[91] 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.[91] Recent studies suggests that hind limb reduction could be due to
mutations in enhancers for the SSH gene,[91] however other studies suggested
that mutations within the Hox Genes or their enhancers could contribute to
snake limblessness.[87] 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[92]
Behavior
Winter dormancy
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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.
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.
Feeding and diet
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 justi es calling them separate modes.[107] 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).[101]
Sidewinding
Main article: Sidewinding
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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 at, or
a sand dune, sidewinding is a modi ed 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.[108][109] 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.[108] 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 1⁄3 of the cost for a lizard to move the same distance.[104] Contrary to
popular belief, there is no evidence that sidewinding is associated with the
sand being hot.[108]
Concertina
Main article: Concertina movement
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.[101][109] 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.[108] The front portion then exes 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.[104] 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.
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Arboreal
Rectilinear
Main article: Rectilinear locomotion
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.[113] 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.[113] 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.[108]
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 in icting 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.[17]: 209 The World Health Organization (WHO) lists snakebite
under the "other neglected conditions" category.[116]
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
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as many as 50,000 recorded initial deaths.[117] 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.[118]
The treatment for a snakebite is as variable as the bite itself. The most
common and effective method is through antivenom (or antivenin), a serum
made from the venom of the snake. Some antivenom is species-speci c
(monovalent) while some is made for use with multiple species in mind
(polyvalent). In the United States for example, all species of venomous
snakes are pit vipers, with the exception of the coral snake. To produce
antivenom, a mixture of the venoms of the different species of rattlesnakes,
copperheads, and cottonmouths is injected into the body of a horse in ever-
increasing dosages until the horse is immunized. Blood is then extracted from
the immunized horse. The serum is separated and further puri ed and freeze-
dried. It is reconstituted with sterile water and becomes antivenom. For this
reason, people who are allergic to horses are more likely to have an allergic
reaction to antivenom.[119] Antivenom for the more dangerous species (such as
mambas, taipans, and cobras) is made in a similar manner in South Africa,
Australia , and India, although these antivenoms are species-speci c.
Snake charmers
Main article: Snake charming
The reverse side of the throne of Pharaoh Tutankhamun with four golden uraeus cobra
gures. Gold with lapis lazuli; Valley of the Kings, Thebes (1347–37 BCE).
fi
Snakes composing a bronze kerykeion from the mythical Longanus river in Sicily
Imperial Japan depicted as an evil snake in a WWII propaganda poster
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.[159]
Medicine
Several compounds from snake venoms are being researched as potential
treatments or preventatives for pain, cancers, arthritis, stroke, heart disease,
hemophilia, and hypertension, and to control bleeding (e.g. during surgery).
[160][161][162]
See also
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• Limbless vertebrates
• List of Serpentes families
• List of snakes
• Ophiology
• Snakebot
• Snake detection theory
• Snake skeleton
• Spinal osteoarthropathy (reptile disease)
• The New Encyclopedia of Snakes
• The Snakes of Europe and Snakes of Europe Wikibooks:Snakes of
Europe, a wikibook
• Venomous snake
Portals:
• Snakes
• Reptiles
• Animals
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Further reading
• Behler JL, King FW (1979). The Audubon Society Field Guide to Reptiles and
Amphibians of North America. New York: Alfred A. Knopf. p. 581.
ISBN 978-0-394-50824-5.
• Bull nch T (2000). Bull nch's Complete Mythology. London: Chancellor Press.
p. 679. ISBN 978-0-7537-0381-6. Archived from the original on 9 February
2009.
• Capula M, Behler JL (1989). Simon & Schuster's Guide to Reptiles and
Amphibians of the World. New York: Simon & Schuster.
ISBN 978-0-671-69098-4.
• Coborn J (1991). The Atlas of Snakes of the World. New Jersey: TFH
Publications. ISBN 978-0-86622-749-0.
• Cogger H, Zweifel R (1992). Reptiles & Amphibians. Sydney: Weldon Owen.
ISBN 978-0-8317-2786-4.
• Conant R, Collins J (1991). A Field Guide to Reptiles and Amphibians Eastern/
Central North America. Boston: Houghton Mif in Company.
ISBN 978-0-395-58389-0.
• Deane, John (1833). The Worship of the Serpent. White sh, Montana:
Kessinger Publishing. p. 412. ISBN 978-1-56459-898-1.
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• Ditmars, Raymond L (1906). Poisonous Snakes of the United States: How to
Distinguish Them. New York: E. R. Sanborn. p. 11.
• Ditmars, Raymond L (1931). Snakes of the World. New York: Macmillan. p. 11.
ISBN 978-0-02-531730-7.
• Ditmars RL (1933). Reptiles of the World: The Crocodilians, Lizards, Snakes,
Turtles and Tortoises of the Eastern and Western Hemispheres. New York:
Macmillan. p. 321.
• Ditmars RL, Bridges W (1935). Snake-Hunters' Holiday. New York: D. Appleton
and Company. p. 309.