122-410: Prolecanitida is an order of extinct ammonoid cephalopods, the major Late Paleozoic group of ammonoids alongside the order Goniatitida . Prolecanitids had narrow shells, discoidal (disc-shaped) to thinly lenticular (lens-shaped). They retained a retrochoanitic siphuncle , a simple form with septal necks extending backwards. As is typical for ammonoids, the siphuncle sits along the ventral margin of
244-427: A "shell vestige" or "gladius". The Incirrina have either a pair of rod-shaped stylets or no vestige of an internal shell, and some squid also lack a gladius. The shelled coleoids do not form a clade or even a paraphyletic group. The Spirula shell begins as an organic structure, and is then very rapidly mineralized. Shells that are "lost" may be lost by resorption of the calcium carbonate component. Females of
366-399: A cloud of dark ink to confuse predators . This sac is a muscular bag which originated as an extension of the hindgut. It lies beneath the gut and opens into the anus, into which its contents – almost pure melanin – can be squirted; its proximity to the base of the funnel means the ink can be distributed by ejected water as the cephalopod uses its jet propulsion. The ejected cloud of melanin
488-451: A diversity of backgrounds. Experiments done in Dwarf chameleons testing these hypotheses showed that chameleon taxa with greater capacity for color change had more visually conspicuous social signals but did not come from more visually diverse habitats, suggesting that color change ability likely evolved to facilitate social signaling, while camouflage is a useful byproduct. Because camouflage
610-529: A flat fan shape with a mucus film between the individual tentacles, while another, Sepioteuthis sepioidea , has been observed putting the tentacles in a circular arrangement. Cephalopods have advanced vision, can detect gravity with statocysts , and have a variety of chemical sense organs. Octopuses use their arms to explore their environment and can use them for depth perception. Most cephalopods rely on vision to detect predators and prey and to communicate with one another. Consequently, cephalopod vision
732-411: A flat plane. The most fundamental difference in spiral form is how strongly successive whorls expand and overlap their predecessors. This can be inferred by the size of the umbilicus, the sunken-in inner part of the coil, exposing older and smaller whorls. Evolute shells have very little overlap, a large umbilicus, and many exposed whorls. Involute shells have strong overlap, a small umbilicus, and only
854-526: A general shape to ammonite tentacles. A contemporary study found an ammonite isolated body, offering for the first time a glimpse into these animals' organs. The smallest ammonoid was Maximites from the Upper Carboniferous . Adult specimens reached only 10 mm (0.39 in) in shell diameter. Few of the ammonites occurring in the lower and middle part of the Jurassic period reached
976-524: A group continued through several major extinction events , although often only a few species survived. Each time, however, this handful of species diversified into a multitude of forms. Ammonite fossils became less abundant during the latter part of the Mesozoic , and although they seemingly survived the Cretaceous–Paleogene extinction event , all known Paleocene ammonite lineages are restricted to
1098-652: A gunshot-like popping noise, thought to function to frighten away potential predators. Cephalopods employ a similar method of propulsion despite their increasing size (as they grow) changing the dynamics of the water in which they find themselves. Thus their paralarvae do not extensively use their fins (which are less efficient at low Reynolds numbers ) and primarily use their jets to propel themselves upwards, whereas large adult cephalopods tend to swim less efficiently and with more reliance on their fins. Early cephalopods are thought to have produced jets by drawing their body into their shells, as Nautilus does today. Nautilus
1220-453: A jet as a propulsion mechanism. Squids do not have the longitudinal muscles that octopus do. Instead, they have a tunic. This tunic is made of layers of collagen and it surrounds the top and the bottom of the mantle. Because they are made of collagen and not muscle, the tunics are rigid bodies that are much stronger than the muscle counterparts. This provides the squids some advantages for jet propulsion swimming. The stiffness means that there
1342-540: A large umbilicus and a generally evolute form. In the later (Upper Mississippian – Triassic) Medlicottioidea , the umbilicus is small, shells tend to be involute, and there is moderate sculpture along the flanks. The oldest known prolecanitids were the family Prolecanitidae, which appeared around the Devonian–Carboniferous boundary and diversified in the Tournaisian stage. One of the most basal members of
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#17327718034571464-406: A length of 8 metres. They may terminate in a broadened, sucker-coated club. The shorter four pairs are termed arms , and are involved in holding and manipulating the captured organism. They too have suckers, on the side closest to the mouth; these help to hold onto the prey. Octopods only have four pairs of sucker-coated arms, as the name suggests, though developmental abnormalities can modify
1586-474: A muscle, which is why they can change their skin hue as rapidly as they do. Coloration is typically stronger in near-shore species than those living in the open ocean, whose functions tend to be restricted to disruptive camouflage . These chromatophores are found throughout the body of the octopus, however, they are controlled by the same part of the brain that controls elongation during jet propulsion to reduce drag. As such, jetting octopuses can turn pale because
1708-451: A narrow ventral lobe, which can range from undivided to tridentate (three-pointed). The saddles are generally rounded, with the first umbilical (or second lateral) saddle often the largest in the suture line. The lobes are usually pointed, though members of the family Daraelitidae acquire a few finely serrated lobes (as characteristic for ceratitic sutures ). The first lateral saddle is proportionally small, though its corresponding lateral lobe
1830-512: A novel mechanism for spectral discrimination in cephalopods was described. This relies on the exploitation of chromatic aberration (wavelength-dependence of focal length). Numerical modeling shows that chromatic aberration can yield useful chromatic information through the dependence of image acuity on accommodation. The unusual off-axis slit and annular pupil shapes in cephalopods enhance this ability by acting as prisms which are scattering white light in all directions. In 2015, molecular evidence
1952-667: A prominent head, and a set of arms or tentacles ( muscular hydrostats ) modified from the primitive molluscan foot. Fishers sometimes call cephalopods " inkfish ", referring to their common ability to squirt ink . The study of cephalopods is a branch of malacology known as teuthology . Cephalopods became dominant during the Ordovician period, represented by primitive nautiloids . The class now contains two, only distantly related, extant subclasses: Coleoidea , which includes octopuses , squid , and cuttlefish ; and Nautiloidea , represented by Nautilus and Allonautilus . In
2074-471: A rare form of physiological color change which utilizes neural control of muscles to change the morphology of their chromatophores. This neural control of chromatophores has evolved convergently in both cephalopods and teleosts fishes. With the exception of the Nautilidae and the species of octopus belonging to the suborder Cirrina , all known cephalopods have an ink sac, which can be used to expel
2196-411: A result of limpets attaching themselves to the shells. However, the triangular formation of the holes, their size and shape, and their presence on both sides of the shells, corresponding to the upper and lower jaws, is more likely evidence of the bite of a medium-sized mosasaur preying upon ammonites. Some ammonites appear to have lived in cold seeps and even reproduced there. The chambered part of
2318-429: A shell-less subclass of cephalopods (squid, cuttlefish, and octopuses), have complex pigment containing cells called chromatophores which are capable of producing rapidly changing color patterns. These cells store pigment within an elastic sac which produces the color seen from these cells. Coleoids can change the shape of this sac, called the cytoelastic sacculus, which then causes changes in the translucency and opacity of
2440-558: A single horny plate or a pair of calcitic plates. In the past, these plates were assumed to serve in closing the opening of the shell in much the same way as an operculum , but more recently they are postulated to have been a jaw apparatus. The plates are collectively termed the aptychus or aptychi in the case of a pair of plates, and anaptychus in the case of a single plate. The paired aptychi were symmetric to one another and equal in size and appearance. Anaptychi are relatively rare as fossils. They are found representing ammonites from
2562-650: A size exceeding 23 cm (9.1 in) in diameter. Much larger forms are found in the later rocks of the upper part of the Jurassic and the lower part of the Cretaceous, such as Titanites from the Portland Stone of Jurassic of southern England, which is often 53 cm (1.74 ft) in diameter, and Parapuzosia seppenradensis of the Cretaceous period of Germany, which is one of the largest-known ammonites, sometimes reaching 2 m (6.6 ft) in diameter. The largest-documented North American ammonite
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#17327718034572684-620: A startling array of fashions. As well as providing camouflage with their background, some cephalopods bioluminesce, shining light downwards to disguise their shadows from any predators that may lurk below. The bioluminescence is produced by bacterial symbionts; the host cephalopod is able to detect the light produced by these organisms. Bioluminescence may also be used to entice prey, and some species use colorful displays to impress mates, startle predators, or even communicate with one another. Cephalopods can change their colors and patterns in milliseconds, whether for signalling (both within
2806-465: Is Baculites , which has a nearly straight shell convergent with the older orthocone nautiloids. Still other species' shells are coiled helically (in two dimensions), similar in appearance to some gastropods (e.g., Turrilites and Bostrychoceras ). Some species' shells are even initially uncoiled, then partially coiled, and finally straight at maturity (as in Australiceras ). Perhaps
2928-506: Is Parapuzosia bradyi from the Cretaceous, with specimens measuring 137 cm (4.5 ft) in diameter. Starting from the mid-Devonian, ammonoids were extremely abundant, especially as ammonites during the Mesozoic era. Many genera evolved and ran their course quickly, becoming extinct in a few million years. Due to their rapid evolution and widespread distribution, ammonoids are used by geologists and paleontologists for biostratigraphy . They are excellent index fossils , and it
3050-626: Is a narrow tubular structure that runs along the shell's outer rim, known as the venter, connecting the chambers of the phragmocone to the body or living chamber. This distinguishes them from living nautiloides ( Nautilus and Allonautilus ) and typical Nautilida , in which the siphuncle runs through the center of each chamber. However the very earliest nautiloids from the Late Cambrian and Ordovician typically had ventral siphuncles like ammonites, although often proportionally larger and more internally structured. The word "siphuncle" comes from
3172-400: Is a notable partial exception in that it tolerates brackish water . Cephalopods are thought to be unable to live in fresh water due to multiple biochemical constraints, and in their >400 million year existence have never ventured into fully freshwater habitats. Cephalopods occupy most of the depth of the ocean, from the abyssal plains to the sea surface, and have also been found in
3294-516: Is acute: training experiments have shown that the common octopus can distinguish the brightness, size, shape, and horizontal or vertical orientation of objects. The morphological construction gives cephalopod eyes the same performance as shark eyes; however, their construction differs, as cephalopods lack a cornea and have an everted retina. Cephalopods' eyes are also sensitive to the plane of polarization of light. Unlike many other cephalopods, nautiluses do not have good vision; their eye structure
3416-463: Is also capable of creating a jet by undulations of its funnel; this slower flow of water is more suited to the extraction of oxygen from the water. When motionless, Nautilus can only extract 20% of oxygen from the water. The jet velocity in Nautilus is much slower than in coleoids , but less musculature and energy is involved in its production. Jet thrust in cephalopods is controlled primarily by
3538-570: Is aragonite. As for other mollusc shells or coral skeletons, the smallest visible units are irregular rounded granules. Cephalopods, as the name implies, have muscular appendages extending from their heads and surrounding their mouths. These are used in feeding, mobility, and even reproduction. In coleoids they number eight or ten. Decapods such as cuttlefish and squid have five pairs. The longer two, termed tentacles , are actively involved in capturing prey; they can lengthen rapidly (in as little as 15 milliseconds ). In giant squid they may reach
3660-683: Is broad and typically bifid (two-pointed). The origin of the Prolecanitida may be found in the Prolobitidae , a family which was originally included in the Anarcestida but recently removed to the Goniatitida. Following their inception, the Prolecanitida divided into two lineages, ranked as superfamilies. In the earlier (Lower Mississippian – Middle Permian) Prolecanitoidea , the shells are fairly smooth and characteristically have
3782-427: Is highly developed, but lacks a solid lens . They have a simple " pinhole " eye through which water can pass. Instead of vision, the animal is thought to use olfaction as the primary sense for foraging , as well as locating or identifying potential mates. All octopuses and most cephalopods are considered to be color blind . Coleoid cephalopods (octopus, squid, cuttlefish) have a single photoreceptor type and lack
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3904-418: Is more efficient, but in environments with little oxygen and in low temperatures, hemocyanin has the upper hand. The hemocyanin molecule is much larger than the hemoglobin molecule, allowing it to bond with 96 O 2 or CO 2 molecules, instead of the hemoglobin's just four. But unlike hemoglobin, which are attached in millions on the surface of a single red blood cell, hemocyanin molecules float freely in
4026-403: Is needed, compensating for their small size. However, organisms which spend most of their time moving slowly along the bottom do not naturally pass much water through their cavity for locomotion; thus they have larger gills, along with complex systems to ensure that water is constantly washing through their gills, even when the organism is stationary. The water flow is controlled by contractions of
4148-439: Is no necessary muscle flexing to keep the mantle the same size. In addition, tunics take up only 1% of the squid mantle's wall thickness, whereas the longitudinal muscle fibers take up to 20% of the mantle wall thickness in octopuses. Also because of the rigidity of the tunic, the radial muscles in squid can contract more forcefully. The mantle is not the only place where squids have collagen. Collagen fibers are located throughout
4270-422: Is occasionally preserved in fossil specimens. The soft body of the creature occupied the largest segments of the shell at the end of the coil. The smaller earlier segments were walled off and the animal could maintain its buoyancy by filling them with gas. Thus, the smaller sections of the coil would have floated above the larger sections. Many ammonite shells have been found with round holes once interpreted as
4392-467: Is often possible to link the rock layer in which they are found to specific geologic time periods . Due to their free-swimming and/or free-floating habits, ammonites often happened to live directly above seafloor waters so poor in oxygen as to prevent the establishment of animal life on the seafloor. When upon death the ammonites fell to this seafloor and were gradually buried in accumulating sediment, bacterial decomposition of these corpses often tipped
4514-539: Is often possible. Their fossil shells usually take the form of planispirals , although some helically spiraled and nonspiraled forms (known as heteromorphs ) have been found. The name "ammonite", from which the scientific term is derived, was inspired by the spiral shape of their fossilized shells, which somewhat resemble tightly coiled rams ' horns. Pliny the Elder ( d. 79 AD near Pompeii) called fossils of these animals ammonis cornua (" horns of Ammon ") because
4636-633: Is often preserved. This type of preservation is found in ammonites such as Hoplites from the Cretaceous Gault clay of Folkestone in Kent, England. The Cretaceous Pierre Shale formation of the United States and Canada is well known for the abundant ammonite fauna it yields, including Baculites , Placenticeras , Scaphites , Hoploscaphites and Jeletzkytes , as well as many uncoiled forms. Many of these also have much or all of
4758-457: Is referred to as a pseudomorph ). This strategy often results in the predator attacking the pseudomorph, rather than its rapidly departing prey. For more information, see Inking behaviors . The ink sac of cephalopods has led to a common name of "inkfish", formerly the pen-and-ink fish. Cephalopods are the only molluscs with a closed circulatory system. Coleoids have two gill hearts (also known as branchial hearts ) that move blood through
4880-413: Is supplemented with fin motion; in the squid, the fins flap each time that a jet is released, amplifying the thrust; they are then extended between jets (presumably to avoid sinking). Oxygenated water is taken into the mantle cavity to the gills and through muscular contraction of this cavity, the spent water is expelled through the hyponome , created by a fold in the mantle. The size difference between
5002-553: Is the first evidence that cephalopod dermal tissues may possess the required combination of molecules to respond to light. Some squids have been shown to detect sound using their statocysts , but, in general, cephalopods are deaf. Most cephalopods possess an assemblage of skin components that interact with light. These may include iridophores, leucophores , chromatophores and (in some species) photophores . Chromatophores are colored pigment cells that expand and contract in accordance to produce color and pattern which they can use in
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5124-538: Is thought to be because the female required a larger body size for egg production. A good example of this sexual variation is found in Bifericeras from the early part of the Jurassic period of Europe . Only recently has sexual variation in the shells of ammonites been recognized. The macroconch and microconch of one species were often previously mistaken for two closely related but different species occurring in
5246-426: Is unknown, but chromatophores are under the control of neural pathways, allowing the cephalopod to coordinate elaborate displays. Together, chromatophores and iridophores are able to produce a large range of colors and pattern displays. Cephalopods utilize chromatophores' color changing ability in order to camouflage themselves. Chromatophores allow Coleoids to blend into many different environments, from coral reefs to
5368-400: Is used for multiple adaptive purposes in cephalopods, color change could have evolved for one use and the other developed later, or it evolved to regulate trade offs within both. Color change is widespread in ectotherms including anoles, frogs, mollusks, many fish, insects, and spiders. The mechanism behind this color change can be either morphological or physiological. Morphological change is
5490-417: Is usually mixed, upon expulsion, with mucus , produced elsewhere in the mantle, and therefore forms a thick cloud, resulting in visual (and possibly chemosensory) impairment of the predator, like a smokescreen . However, a more sophisticated behavior has been observed, in which the cephalopod releases a cloud, with a greater mucus content, that approximately resembles the cephalopod that released it (this decoy
5612-591: The Neo-Latin siphunculus , meaning "little siphon". Originating from within the bactritoid nautiloids, the ammonoid cephalopods first appeared in the Devonian ( circa 409 million years ago (Mya)) and became extinct shortly after Cretaceous (66 Mya). The classification of ammonoids is based in part on the ornamentation and structure of the septa comprising their shells' gas chambers. The Ammonoidea can be divided into six orders, listed here starting with
5734-768: The Paleocene epoch (65–61 Ma). Goniatites, which were a dominant component of Early and Middle Permian faunas, became rare in the Late Permian, and no goniatite is thought to have crossed into the Triassic. Ceratitida originated during the Middle Permian, likely from the Daraelitidae , and radiated in the Late Permian. In the aftermath of the Permian–Triassic extinction event , Ceratitids represent
5856-638: The Solnhofen Limestone , their soft-part record is surprisingly sparse. Beyond a tentative ink sac and possible digestive organs, no soft parts were known until 2021. When neutron imaging was used on a fossil found in 1998, part of the musculature became visible and showed they were able to retract themselves into the shell for protection, and that the retractor muscles and hyponome that work together to enable jet propulsion in nautilus worked independently in ammonites. The reproductive organs show possible traces of spermatophores, which would support
5978-433: The buoyancy of the shell and thereby rise or descend in the water column. A primary difference between ammonites and nautiloids is the siphuncle of ammonites (excepting Clymeniina ) runs along the ventral periphery of the septa and camerae (i.e., the inner surface of the outer axis of the shell), while the siphuncle of nautiloids runs more or less through the center of the septa and camerae. One feature found in shells of
6100-416: The hadal zone . Their diversity is greatest near the equator (~40 species retrieved in nets at 11°N by a diversity study) and decreases towards the poles (~5 species captured at 60°N). Cephalopods are widely regarded as the most intelligent of the invertebrates and have well developed senses and large brains (larger than those of gastropods ). The nervous system of cephalopods is the most complex of
6222-583: The sparkling enope squid ( Watasenia scintillans ). It achieves color vision with three photoreceptors , which are based on the same opsin , but use distinct retinal molecules as chromophores: A1 (retinal), A3 (3-dehydroretinal), and A4 (4-hydroxyretinal). The A1-photoreceptor is most sensitive to green-blue (484 nm), the A2-photoreceptor to blue-green (500 nm), and the A4-photoreceptor to blue (470 nm) light. In 2015,
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#17327718034576344-653: The Ceratitina from the Triassic; and the Ammonitina, Lytoceratina and Phylloceratina from the Jurassic and Cretaceous. In subsequent taxonomies, these are sometimes regarded as orders within the subclass Ammonoidea. Because ammonites and their close relatives are extinct, little is known about their way of life. Their soft body parts are very rarely preserved in any detail. Nonetheless, much has been worked out by examining ammonoid shells and by using models of these shells in water tanks. Many ammonoids probably lived in
6466-612: The Coleoidea, the molluscan shell has been internalized or is absent, whereas in the Nautiloidea, the external shell remains. About 800 living species of cephalopods have been identified. Two important extinct taxa are the Ammonoidea (ammonites) and Belemnoidea (belemnites). Extant cephalopods range in size from the 10 mm (0.3 in) Idiosepius thailandicus to the 700 kilograms (1,500 lb) heavy Colossal squid ,
6588-540: The Devonian period through those of the Cretaceous period. Calcified aptychi only occur in ammonites from the Mesozoic era. They are almost always found detached from the shell, and are only very rarely preserved in place. Still, sufficient numbers have been found closing the apertures of fossil ammonite shells as to leave no doubt as to their identity as part of the anatomy of an ammonite. Large numbers of detached aptychi occur in certain beds of rock (such as those from
6710-605: The Egyptian god Ammon ( Amun ) was typically depicted wearing rams' horns. Often, the name of an ammonite genus ends in - ceras , which is from κέρας ( kéras ) meaning "horn". Ammonites (subclass Ammonoidea) can be distinguished by their septa, the dividing walls that separate the chambers in the phragmocone, by the nature of their sutures where the septa join the outer shell wall, and in general by their siphuncles . Ammonoid septa characteristically have bulges and indentations and are to varying degrees convex when seen from
6832-414: The Goniatitida and the Prolecanitida and their Mesozoic descendants. Ammonoidea Ammonoids are extinct spiral shelled cephalopods comprising the subclass Ammonoidea . They are more closely related to living coleoids (i.e., octopuses , squid and cuttlefish ) than they are to shelled nautiloids (such as the living Nautilus ). The earliest ammonoids appeared during the Devonian , with
6954-519: The Mesozoic in the Alps ). These rocks are usually accumulated at great depths. The modern Nautilus lacks any calcitic plate for closing its shell, and only one extinct nautiloid genus is known to have borne anything similar. Nautilus does, however, have a leathery head shield (the hood) which it uses to cover the opening when it retreats inside. There are many forms of aptychus, varying in shape and
7076-556: The ability to determine color by comparing detected photon intensity across multiple spectral channels. When camouflaging themselves, they use their chromatophores to change brightness and pattern according to the background they see, but their ability to match the specific color of a background may come from cells such as iridophores and leucophores that reflect light from the environment. They also produce visual pigments throughout their body and may sense light levels directly from their body. Evidence of color vision has been found in
7198-452: The acidity of the organic shell matrix (see Mollusc shell ); shell-forming cephalopods have an acidic matrix, whereas the gladius of squid has a basic matrix. The basic arrangement of the cephalopod outer wall is: an outer (spherulitic) prismatic layer, a laminar (nacreous) layer and an inner prismatic layer. The thickness of every layer depends on the taxa. In modern cephalopods, the Ca carbonate
7320-434: The air for distances of up to 50 metres (160 ft). While cephalopods are not particularly aerodynamic, they achieve these impressive ranges by jet-propulsion; water continues to be expelled from the funnel while the organism is in the air. The animals spread their fins and tentacles to form wings and actively control lift force with body posture. One species, Todarodes pacificus , has been observed spreading tentacles in
7442-440: The ammonite shell is called a phragmocone . It contains a series of progressively larger chambers, called camerae (sing. camera) that are divided by thin walls called septa (sing. septum). Only the last and largest chamber, the body chamber , was occupied by the living animal at any given moment. As it grew, it added newer and larger chambers to the open end of the coil. Where the outer whorl of an ammonite shell largely covers
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#17327718034577564-456: The ammonoid suture line (the intersection of the septum with the outer shell) is variably folded, forming saddles ("peaks" that point towards the aperture) and lobes ("valleys" which point away from the aperture). The suture line has four main regions. The external or ventral region refers to sutures along the lower (outer) edge of the shell, where the left and right suture lines meet. The external (or ventral) saddle, when present, lies directly on
7686-474: The animal's life; additional shell layers covered it. The majority of ammonoid specimens, especially those of the Paleozoic era, are preserved only as internal molds; the outer shell (composed of aragonite ) has been lost during the fossilization process. Only in these internal-mould specimens can the suture lines be observed; in life, the sutures would have been hidden by the outer shell. The ammonoids as
7808-454: The appearance of their surroundings is notable given that cephalopods' vision is monochromatic. Cephalopods also use their fine control of body coloration and patterning to perform complex signaling displays for both conspecific and intraspecific communication. Coloration is used in concert with locomotion and texture to send signals to other organisms. Intraspecifically this can serve as a warning display to potential predators. For example, when
7930-403: The bloodstream. Cephalopods exchange gases with the seawater by forcing water through their gills, which are attached to the roof of the organism. Water enters the mantle cavity on the outside of the gills, and the entrance of the mantle cavity closes. When the mantle contracts, water is forced through the gills, which lie between the mantle cavity and the funnel. The water's expulsion through
8052-517: The body cavity; others, like some fish, accumulate oils in the liver; and some octopuses have a gelatinous body with lighter chloride ions replacing sulfate in the body chemistry. Squids are the primary sufferers of negative buoyancy in cephalopods. The negative buoyancy means that some squids, especially those whose habitat depths are rather shallow, have to actively regulate their vertical positions. This means that they must expend energy, often through jetting or undulations, in order to maintain
8174-582: The brain is unable to achieve both controlling elongation and controlling the chromatophores. Most octopuses mimic select structures in their field of view rather than becoming a composite color of their full background. Evidence of original coloration has been detected in cephalopod fossils dating as far back as the Silurian ; these orthoconic individuals bore concentric stripes, which are thought to have served as camouflage. Devonian cephalopods bear more complex color patterns, of unknown function. Coleoids,
8296-401: The capillaries of the gills . A single systemic heart then pumps the oxygenated blood through the rest of the body. Like most molluscs, cephalopods use hemocyanin , a copper-containing protein, rather than hemoglobin , to transport oxygen. As a result, their blood is colorless when deoxygenated and turns blue when bonded to oxygen. In oxygen-rich environments and in acidic water, hemoglobin
8418-436: The cavity by entering not only through the orifices, but also through the funnel. Squid can expel up to 94% of the fluid within their cavity in a single jet thrust. To accommodate the rapid changes in water intake and expulsion, the orifices are highly flexible and can change their size by a factor of twenty; the funnel radius, conversely, changes only by a factor of around 1.5. Some octopus species are also able to walk along
8540-561: The cell. By rapidly changing multiple chromatophores of different colors, cephalopods are able to change the color of their skin at astonishing speeds, an adaptation that is especially notable in an organism that sees in black and white. Chromatophores are known to only contain three pigments, red, yellow, and brown, which cannot create the full color spectrum. However, cephalopods also have cells called iridophores, thin, layered protein cells that reflect light in ways that can produce colors chromatophores cannot. The mechanism of iridophore control
8662-399: The cephalopod mantle have been widely used for many years as experimental material in neurophysiology ; their large diameter (due to lack of myelination ) makes them relatively easy to study compared with other animals. Many cephalopods are social creatures; when isolated from their own kind, some species have been observed shoaling with fish. Some cephalopods are able to fly through
8784-419: The delicate balance of local redox conditions sufficiently to lower the local solubility of minerals dissolved in the seawater, notably phosphates and carbonates . The resulting spontaneous concentric precipitation of minerals around a fossil, a concretion , is responsible for the outstanding preservation of many ammonite fossils. When ammonites are found in clays , their original mother-of-pearl coating
8906-420: The dominant group of Triassic ammonites. Cephalopod A cephalopod / ˈ s ɛ f ə l ə p ɒ d / is any member of the molluscan class Cephalopoda / s ɛ f ə ˈ l ɒ p ə d ə / ( Greek plural κεφαλόποδες , kephalópodes ; "head-feet") such as a squid , octopus , cuttlefish , or nautilus . These exclusively marine animals are characterized by bilateral body symmetry ,
9028-410: The earliest genera to much more complex-sutured genera in the late Paleozoic. The increase in suture complexity over the 108 m.y. duration resulted from the iterative of addition of umbilical lobes, increasing serration of lobes, and the subdivision of lateral and ventral lobes. As many as 12–15 replicate, U-shaped umbilical lobes were added to the sutures during both ontogeny and phylogeny, originating at
9150-469: The expansion of the mantle at the end of the jet. In some tests, the collagen has been shown to be able to begin raising mantle pressure up to 50ms before muscle activity is initiated. These anatomical differences between squid and octopuses can help explain why squid can be found swimming comparably to fish while octopuses usually rely on other forms of locomotion on the sea floor such as bipedal walking, crawling, and non-jetting swimming. Nautiluses are
9272-466: The first heteromorph ammonoid fossils belongs to the genus Rhabdoceras. The three other heteromorphic genera were Hannaoceras, Cochloceras and Choristoceras. All of them went extinct at the end of Triassic. In the Jurassic an uncoiled shell was found in the Spiroceratoidea, but by the end of Cretaceous the only heteromorph ammonites remaining belonged to the suborder Ancyloceratina. One example
9394-420: The first saddle and lobe pair past the external region as the suture line extends up the side of the shell. The lateral saddle and lobe are usually larger than the ventral saddle and lobe. Additional lobes developing towards the inner edge of a whorl are labelled umbilical lobes, which increase in number through ammonoid evolution as well as an individual ammonoid's development. In many cases the distinction between
9516-413: The form of jetting. The composition of these mantles differs between the two families, however. In octopuses, the mantle is made up of three muscle types: longitudinal, radial, and circular. The longitudinal muscles run parallel to the length of the octopus and they are used in order to keep the mantle the same length throughout the jetting process. Given that they are muscles, it can be noted that this means
9638-433: The front, distinguishing them from nautiloid septa, which are typically simple concave, dish-shaped structures. The topology of the septa, especially around the rim, results in the various suture patterns found. The septal curvature in nautiloids and ammonoids also differ in that the septa curves towards the opening in nautiloids, and away from the opening in ammоnoids. While nearly all nautiloids show gently curving sutures,
9760-456: The funnel can be used to power jet propulsion. If respiration is used concurrently with jet propulsion, large losses in speed or oxygen generation can be expected. The gills, which are much more efficient than those of other mollusks, are attached to the ventral surface of the mantle cavity. There is a trade-off with gill size regarding lifestyle. To achieve fast speeds, gills need to be small – water will be passed through them quickly when energy
9882-503: The hypothesis that the microconchs were males. They likely bore a radula and beak, a marginal siphuncle and ten arms. They operated by direct development with sexual reproduction, were carnivorous, and had a crop for food storage. They are unlikely to have dwelt in fresh or brackish water. Many ammonites were likely filter feeders , so adaptations associated with this lifestyle like sieves probably occurred. A 2021 study found ammonite specimens with preserved hook-like suckers, providing
10004-400: The invertebrates and their brain-to-body-mass ratio falls between that of endothermic and ectothermic vertebrates. Captive cephalopods have also been known to climb out of their aquaria, maneuver a distance of the lab floor, enter another aquarium to feed on captive crabs, and return to their own aquarium. The brain is protected in a cartilaginous cranium. The giant nerve fibers of
10126-511: The largest and most recent whorls are exposed. Shell structure can be broken down further by the width of the shell, with implications for hydrodynamic efficiency. Major shell forms include: Ammonites vary greatly in the ornamentation (surface relief) of their shells. Some may be smooth and relatively featureless, except for growth lines, resembling that of the modern Nautilus . In others, various patterns of spiral ridges, ribs, nodes, or spines are presented. This type of complex ornamentation of
10248-508: The largest extant invertebrate . There are over 800 extant species of cephalopod, although new species continue to be described. An estimated 11,000 extinct taxa have been described, although the soft-bodied nature of cephalopods means they are not easily fossilised. Cephalopods are found in all the oceans of Earth. None of them can tolerate fresh water , but the brief squid, Lolliguncula brevis , found in Chesapeake Bay ,
10370-438: The last species vanishing during or soon after the Cretaceous–Paleogene extinction event . They are often called ammonites , which is most frequently used for members of the order Ammonitida , the only remaining group of ammonoids from the Jurassic up until their extinction. Ammonites are excellent index fossils , and linking the rock layer in which a particular species or genus is found to specific geologic time periods
10492-510: The lateral and umbilical regions are unclear; new umbilical features can develop from subdivisions of other umbilical features, or from subdivisions of lateral features. Lobes and saddles which are so far towards the center of the whorl that they are covered up by succeeding whorls are labelled internal (or dorsal) lobes and saddles. Three major types of suture patterns are found in the Ammonoidea: The siphuncle in most ammonoids
10614-434: The lower midline of the shell. As a result, it is often called the median saddle. On suture diagrams the median saddle is supplied with an arrow which points towards the aperture. The median saddle is edged by fairly small external (or ventral) lobes. The earliest ammonoids lacked a median saddle and instead had a single midline ventral lobe, which in later forms is split into two or more components. The lateral region involves
10736-472: The maximum diameter of the funnel orifice (or, perhaps, the average diameter of the funnel) and the diameter of the mantle cavity. Changes in the size of the orifice are used most at intermediate velocities. The absolute velocity achieved is limited by the cephalopod's requirement to inhale water for expulsion; this intake limits the maximum velocity to eight body-lengths per second, a speed which most cephalopods can attain after two funnel-blows. Water refills
10858-432: The modern Nautilus is the variation in the shape and size of the shell according to the sex of the animal, the shell of the male being slightly smaller and wider than that of the female. This sexual dimorphism is thought to be an explanation for the variation in size of certain ammonite shells of the same species, the larger shell (the macroconch ) being female, and the smaller shell (the microconch ) being male. This
10980-543: The most extreme and bizarre-looking example of a heteromorph is Nipponites , which appears to be a tangle of irregular whorls lacking any obvious symmetric coiling. Upon closer inspection, though, the shell proves to be a three-dimensional network of connected "U" shapes. Nipponites occurs in rocks of the upper part of the Cretaceous in Japan and the United States. Some ammonites have been found in association with
11102-575: The most primitive and going to the more derived: In some classifications, these are left as suborders, included in only three orders: Goniatitida , Ceratitida and Ammonitida . The Treatise on Invertebrate Paleontology (Part L, 1957) divides the Ammonoidea, regarded simply as an order, into eight suborders, the Anarcestina, Clymeniina, Goniatitina and Prolecanitina from the Paleozoic;
11224-404: The non threatening herbivorous parrotfish to approach unaware prey. The octopus Thaumoctopus mimicus is known to mimic a number of different venomous organisms it cohabitates with to deter predators. While background matching, a cephalopod changes its appearance to resemble its surroundings, hiding from its predators or concealing itself from prey. The ability to both mimic other organisms and match
11346-413: The octopus Callistoctopus macropus is threatened, it will turn a bright red brown color speckled with white dots as a high contrast display to startle predators. Conspecifically, color change is used for both mating displays and social communication. Cuttlefish have intricate mating displays from males to females. There is also male to male signaling that occurs during competition over mates, all of which are
11468-443: The octopus genus Argonauta secrete a specialized paper-thin egg case in which they reside, and this is popularly regarded as a "shell", although it is not attached to the body of the animal and has a separate evolutionary origin. The largest group of shelled cephalopods, the ammonites , are extinct, but their shells are very common as fossils . The deposition of carbonate, leading to a mineralized shell, appears to be related to
11590-444: The octopus must actively flex the longitudinal muscles during jetting in order to keep the mantle at a constant length. The radial muscles run perpendicular to the longitudinal muscles and are used to thicken and thin the wall of the mantle. Finally, the circular muscles are used as the main activators in jetting. They are muscle bands that surround the mantle and expand/contract the cavity. All three muscle types work in unison to produce
11712-497: The only extant cephalopods with a true external shell. However, all molluscan shells are formed from the ectoderm (outer layer of the embryo); in cuttlefish ( Sepia spp.), for example, an invagination of the ectoderm forms during the embryonic period, resulting in a shell ( cuttlebone ) that is internal in the adult. The same is true of the chitinous gladius of squid and octopuses. Cirrate octopods have arch-shaped cartilaginous fin supports , which are sometimes referred to as
11834-781: The open water of ancient seas, rather than at the sea bottom, because their fossils are often found in rocks laid down under conditions where no bottom-dwelling life is found. In general, they appear to have inhabited the upper 250 meters of the water column. Many of them (such as Oxynoticeras ) are thought to have been good swimmers, with flattened, discus-shaped, streamlined shells, although some ammonoids were less effective swimmers and were likely to have been slow-swimming bottom-dwellers. Synchrotron analysis of an aptychophoran ammonite revealed remains of isopod and mollusc larvae in its buccal cavity, indicating at least this kind of ammonite fed on plankton . They may have avoided predation by squirting ink , much like modern cephalopods; ink
11956-455: The order was Protocanites , which has been (likely erroneously) reported from the latest Devonian Louisiana Limestone of Missouri . The prolecanitoid family Daraelitidae is the probable source for the order Ceratitida , beginning with the family Xenodiscidae in the Middle Permian. Not counting their ceratite descendants, the youngest known prolecanitids were Episageceras and Latisageceras , two Early Triassic medlicottioid genera in
12078-478: The original shell, as well as the complete body chamber, still intact. Many Pierre Shale ammonites, and indeed many ammonites throughout earth history, are found inside concretions . Other fossils, such as many found in Madagascar and Alberta , Canada display iridescence . These iridescent ammonites are often of gem quality ( ammolite ) when polished. In no case would this iridescence have been visible during
12200-440: The other muscle fibers in the mantle. These collagen fibers act as elastics and are sometimes named "collagen springs". As the name implies, these fibers act as springs. When the radial and circular muscles in the mantle contract, they reach a point where the contraction is no longer efficient to the forward motion of the creature. In such cases, the excess contraction is stored in the collagen which then efficiently begins or aids in
12322-442: The posterior and anterior ends of this organ control the speed of the jet the organism can produce. The velocity of the organism can be accurately predicted for a given mass and morphology of animal. Motion of the cephalopods is usually backward as water is forced out anteriorly through the hyponome, but direction can be controlled somewhat by pointing it in different directions. Some cephalopods accompany this expulsion of water with
12444-461: The preceding whorls, the specimen is said to be involute (e.g., Anahoplites ). Where it does not cover those preceding, the specimen is said to be evolute (e.g., Dactylioceras ). A thin living tube called a siphuncle passed through the septa, extending from the ammonite's body into the empty shell chambers. Through a hyperosmotic active transport process, the ammonite emptied water out of these shell chambers. This enabled it to control
12566-407: The product of chromatophore coloration displays. There are two hypotheses about the evolution of color change in cephalopods. One hypothesis is that the ability to change color may have evolved for social, sexual, and signaling functions. Another explanation is that it first evolved because of selective pressures encouraging predator avoidance and stealth hunting. For color change to have evolved as
12688-431: The radial and circular mantle cavity muscles. The gills of cephalopods are supported by a skeleton of robust fibrous proteins; the lack of mucopolysaccharides distinguishes this matrix from cartilage. The gills are also thought to be involved in excretion, with NH 4 being swapped with K from the seawater. While most cephalopods can move by jet propulsion, this is a very energy-consuming way to travel compared to
12810-441: The result of a change in the density of pigment containing cells and tends to change over longer periods of time. Physiological change, the kind observed in cephalopod lineages, is typically the result of the movement of pigment within the chromatophore, changing where different pigments are localized within the cell. This physiological change typically occurs on much shorter timescales compared to morphological change. Cephalopods have
12932-439: The result of natural selection different parameters would have to be met. For one, you would need some phenotypic diversity in body patterning among the population. The species would also need to cohabitate with predators which rely on vision for prey identification. These predators should have a high range of visual sensitivity, detecting not just motion or contrast but also colors. The habitats they occupy would also need to display
13054-424: The result of social selection the environment of cephalopods' ancestors would have to fit a number of criteria. One, there would need to be some kind of mating ritual that involved signaling. Two, they would have to experience demonstrably high levels of sexual selection. And three, the ancestor would need to communicate using sexual signals that are visible to a conspecific receiver. For color change to have evolved as
13176-549: The same class. Octopuses are generally not seen as active swimmers; they are often found scavenging the sea floor instead of swimming long distances through the water. Squids, on the other hand, can be found to travel vast distances, with some moving as much as 2000 km in 2.5 months at an average pace of 0.9 body lengths per second. There is a major reason for the difference in movement type and efficiency: anatomy. Both octopuses and squids have mantles (referenced above) which function towards respiration and locomotion in
13298-399: The same depth. As such, the cost of transport of many squids are quite high. That being said, squid and other cephalopod that dwell in deep waters tend to be more neutrally buoyant which removes the need to regulate depth and increases their locomotory efficiency. The Macrotritopus defilippi , or the sand-dwelling octopus, was seen mimicking both the coloration and the swimming movements of
13420-494: The same rocks. However, because the dimorphic sizes are so consistently found together, they are more likely an example of sexual dimorphism within the same species. Whorl width in the body chamber of many groups of ammonites, as expressed by the width:diameter ratio, is another sign of dimorphism. This character has been used to separate "male" (Largiventer conch "L") from "female" (Leviventer conch "l"). The majority of ammonite species feature planispiral shells, tightly coiled in
13542-452: The sand-dwelling flounder Bothus lunatus to avoid predators. The octopuses were able to flatten their bodies and put their arms back to appear the same as the flounders as well as move with the same speed and movements. Females of two species, Ocythoe tuberculata and Haliphron atlanticus , have evolved a true swim bladder . Two of the categories of cephalopods, octopus and squid, are vastly different in their movements despite being of
13664-446: The sandy sea floor. The color change of chromatophores works in concert with papillae, epithelial tissue which grows and deforms through hydrostatic motion to change skin texture. Chromatophores are able to perform two types of camouflage, mimicry and color matching. Mimicry is when an organism changes its appearance to appear like a different organism. The squid Sepioteuthis sepioide has been documented changing its appearance to appear as
13786-479: The sculpture of the inner and outer surfaces, but because they are so rarely found in position within the shell of the ammonite it is often unclear to which species of ammonite one kind of aptychus belongs. A number of aptychi have been given their own genus and even species names independent of their unknown owners' genus and species, pending future discovery of verified occurrences within ammonite shells. Although ammonites do occur in exceptional lagerstatten such as
13908-489: The seabed. Squids and cuttlefish can move short distances in any direction by rippling of a flap of muscle around the mantle. While most cephalopods float (i.e. are neutrally buoyant or nearly so; in fact most cephalopods are about 2–3% denser than seawater ), they achieve this in different ways. Some, such as Nautilus , allow gas to diffuse into the gap between the mantle and the shell; others allow purer water to ooze from their kidneys, forcing out denser salt water from
14030-415: The shell is especially evident in the later ammonites of the Cretaceous. Ammonoids with a shell shape diverging from the typical planispiral form are known as heteromorphs , instead forming a conch with detached whorls (open coiling) or non-planispiral coiling. These types of shells evolved four times in ammonoids, with the first forms appearing already in the Devonian period. In late Norian age in Triassic
14152-626: The shell. Prolecanitids form a relatively small and stable order within the Ammonoidea , with 43 named genera and about 1250 species. They were a long-ranging lineage, surviving for about 108 m.y. stretching from the Devonian – Carboniferous boundary to the Early Triassic . Although not as diverse as their goniatitid contemporaries, the Prolecanatida provided the stock from which all later Mesozoic ammonoids were derived. Most prolecanitids had goniatitic sutures . The sutures start at
14274-440: The species and for warning ) or active camouflage , as their chromatophores are expanded or contracted. Although color changes appear to rely primarily on vision input, there is evidence that skin cells, specifically chromatophores , can detect light and adjust to light conditions independently of the eyes. The octopus changes skin color and texture during quiet and active sleep cycles. Cephalopods can use chromatophores like
14396-461: The subfamily Episageceratinae . Prolecanitids showed long-term, gradual changes in shell geometry. Likewise, they utilized a more limited set of available forms (a smaller morphospace) as compared to the dominant goniatitids. Prolecanitid genera averaged 14.7 million years in duration, as compared to 5.7 million years for Upper Carboniferous goniatitids. Suture morphology in the Prolecanitida changed dramatically over time, from very simple sutures in
14518-403: The tail propulsion used by fish. The efficiency of a propeller -driven waterjet (i.e. Froude efficiency ) is greater than a rocket . The relative efficiency of jet propulsion decreases further as animal size increases; paralarvae are far more efficient than juvenile and adult individuals. Since the Paleozoic era , as competition with fish produced an environment where efficient motion
14640-461: The umbilicus and migrating outward across the flanks. Suture patterns in Prolecanitida evolved differently than in the Goniatitda, by increasing the number of umbilical lobes rather than by subdivision of the lateral saddle. Moreover, the body chamber in Prolecanitida was comparatively short, taking up only about half of the largest whorl. This complicates the question of the relationship between
14762-463: Was crucial to survival, jet propulsion has taken a back role, with fins and tentacles used to maintain a steady velocity. Whilst jet propulsion is never the sole mode of locomotion, the stop-start motion provided by the jets continues to be useful for providing bursts of high speed – not least when capturing prey or avoiding predators . Indeed, it makes cephalopods the fastest marine invertebrates, and they can out-accelerate most fish. The jet
14884-401: Was published indicating that cephalopod chromatophores are photosensitive; reverse transcription polymerase chain reactions (RT-PCR) revealed transcripts encoding rhodopsin and retinochrome within the retinas and skin of the longfin inshore squid ( Doryteuthis pealeii ), and the common cuttlefish ( Sepia officinalis ) and broadclub cuttlefish ( Sepia latimanus ). The authors claim this
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