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Hermit crab

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87-684: Hermit crabs are anomuran decapod crustaceans of the superfamily Paguroidea that have adapted to occupy empty scavenged mollusc shells to protect their fragile exoskeletons. There are over 800 species of hermit crab, most of which possess an asymmetric abdomen concealed by a snug-fitting shell. Hermit crabs' soft (non- calcified ) abdominal exoskeleton means they must occupy shelter produced by other organisms or risk being defenseless. The strong association between hermit crabs and their shelters has significantly influenced their biology. Almost 800 species carry mobile shelters (most often calcified snail shells ); this protective mobility contributes to

174-536: A convenient and nutritionally balanced foundation for a hermit crab's diet. These foods are specially formulated to meet the species' specific needs and should form the majority of their daily intake. It is important to select a product that is designed for hermit crabs, as general pet foods may lack the necessary nutrients. In the wild, hermit crabs are omnivorous scavengers, feeding on a varied diet of plant matter, decaying organic material, small invertebrates, and marine detritus. They look for algae, seaweed, fruits, and

261-732: A family within Paguroidea. The molecular data has disproven an alternate view based on morphological arguments that the Lithodidae (king crabs) nest with the Hapalogastridae in a separate superfamily, Lithodoidea. As such, in 2023, the family Lithodidae was placed back into Paguroidea after having been moved out of it in 2007. Nine families are formally recognized in the superfamily Paguroidea, containing around 1200 species in total in 135 genera. The placement of Paguroidea within Anomura can be shown in

348-411: 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

435-512: 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

522-519: 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

609-595: A healthy hermit crab. A key component of a hermit crab's diet is calcium, which supports the health and hardness of their exoskeleton. Crushed cuttlebone, calcium-rich commercial supplements, or even ground eggshells can be provided to meet this need. Additionally, carotene-rich foods such as carrots or squash are essential for promoting the development of their reddish-orange exoskeleton. Occasional treats can be offered to hermit crabs to enrich their diet. These may include nuts (such as almonds or sunflower seeds), seeds, and dried seaweed. While these treats should not make up

696-721: A large portion of the diet, they can provide additional nutrients and variety. Hermit crabs are nocturnal feeders, so they should be provided with food in the evening, and any uneaten food should be removed the next morning to prevent spoilage. It is important to monitor the amount of food provided, as hermit crabs tend to eat small portions over extended periods and may consume food slowly. In addition to solid food, hermit crabs require constant access to both freshwater and saltwater for hydration and health. These should be provided in separate dishes to meet their needs for drinking and bathing. As hermit crabs grow, they require larger shells. Since suitable intact gastropod shells are sometimes

783-402: A limited resource, competition often occurs between hermit crabs for shells. The availability of empty shells at any given place depends on the relative abundance of gastropods and hermit crabs, matched for size. An equally important issue is the population of organisms that prey upon gastropods and leave the shells intact. Hermit crabs kept together may fight or kill a competitor to gain access to

870-399: A number of "raps", the defender may come out of its shell completely, usually positioning itself of one of the shells. The attacker then checks the now free shell, and then changes shell rapidly. As the crab tries its new shell, it usually holds its old shell, as it may decide to come back to the old one. The defeated crab then runs to the empty shell. If the defeated crab does not stay close to

957-411: 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

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1044-558: 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

1131-637: 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

1218-409: A very social and peaceful crab. The Purple Pincher ( Coenobita clypeatus ) is a purple and orange crab that is typically found near the shore and especially in the tropical islands. While they are also nocturnal these crabs have aggressive behaviors as well as cannibal tendencies. They forage in a big groups, and are able to eat anything from fish to wood. Though they are terrestrial they travel back to

1305-458: 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

1392-506: 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

1479-550: Is Platykotta , from the Norian – Rhaetian (Late Triassic) Period in the United Arab Emirates . [REDACTED] [REDACTED] [REDACTED] [REDACTED] [REDACTED] Ammonite 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

1566-410: Is a behavior observed in all hermit crabs. It is a process in which the attacker hermit crab attempts to steal the shell of the victim, using a fairly intricate process. It usually only occurs if there is no empty shell suitable for the growing hermit crab. These fights are usually between the same species, though they can also occur between two separate species. If the defending crab does not retreat to

1653-506: Is brought down. This movement is sometimes called an "ambulatory poke". They also use their chelipeds as a warning display, usually used in two distinct variations. The first one consists of the crab lifting its whole body (shell included), and spreading its legs, then moving its cheliped forward until the dactylus (top part of the claw) is perpendicular with the ground. This movement is usually called an "cheliped presentation" This position may be more distinct in some species, such as those in

1740-612: 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

1827-419: 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 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

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1914-422: 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

2001-467: 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

2088-614: 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

2175-431: Is reduced in size, and often hidden inside the gill chamber (under the carapace ) to be used for cleaning the gills. Since this arrangement is very rare in true crabs (for example, the small family Hexapodidae ), a "crab" with only eight visible pereiopods is generally an anomuran. The infraorder Anomura belongs to the group Reptantia , which consists of the walking/crawling decapods ( lobsters and crabs). There

2262-527: 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

2349-506: Is wide acceptance from morphological and molecular data that Anomura and Brachyura ("true" crabs) are sister taxa , together making up the clade Meiura. Anomura likely diverged from Brachyura in the Late Triassic period, with the earliest discovered Anomuran fossil Platykotta akaina dating from the Norian – Rhaetian aged Ghalilah Formation of the United Arab Emirates . The cladogram below shows Anomura's placement within

2436-629: 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 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

2523-637: The Late Cretaceous . Before that time, at least some hermit crabs used ammonite shells instead, as shown by a specimen of Palaeopagurus vandenengeli from the Speeton Clay Formation , Yorkshire , UK , from the Lower Cretaceous , as well as a specimen of a diogenid hermit crab from the Upper Jurassic of Russia. The earliest record of the superfamily extends back to the earliest part of

2610-739: 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

2697-629: 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

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2784-433: 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

2871-764: The cladogram below, which also shows the king crabs of Lithodidae as sister taxon to the hermit crabs of Paguridae : Brachyura ("true" crabs) [REDACTED] Porcellanidae (porcelain crabs) [REDACTED] Munididae (squat lobsters) [REDACTED] Parapaguridae (deep water sea anemone hermit crabs) [REDACTED] Eumunididae (squat lobster-like) [REDACTED] Hippidae (mole crabs or sand crabs) [REDACTED] Lithodidae (king crabs) [REDACTED] Paguridae (hermit crabs) [REDACTED] Diogenidae (left-handed hermit crabs) [REDACTED] Coenobitidae (terrestrial hermit crabs) [REDACTED] The fossil record of in situ hermit crabs using gastropod shells stretches back to

2958-695: The Ammonoidea, regarded simply as an order, into eight suborders, the Anarcestina, Clymeniina, Goniatitina and Prolecanitina from the Paleozoic; 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

3045-535: 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

3132-506: The Elder ( d. 79 AD near Pompeii) called fossils of these animals ammonis cornua (" horns of Ammon ") because 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

3219-486: The Jurassic, with the oldest known species being Schobertella hoelderi from the late Hettangian of Germany. Hermit crabs can be informally divided into two groups: aquatic hermit crabs and terrestrial hermit crabs. The first group, the land hermit crabs, spend most of their life on land as terrestrial species in tropical areas, though even they require access to both freshwater and saltwater to keep their gills damp or wet to survive and to reproduce. They belong to

3306-510: 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

3393-440: 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

3480-469: 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

3567-415: 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 the lower midline of the shell. As a result, it is often called the median saddle. On suture diagrams

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3654-571: 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 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

3741-419: 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 the front, distinguishing them from nautiloid septa, which are typically simple concave, dish-shaped structures. The topology of the septa, especially around

3828-419: 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

3915-600: The diversity and multitude of these crustaceans which are found in almost all marine environments. In most species, development involves metamorphosis from symmetric, free-swimming larvae to morphologically asymmetric, benthic -dwelling, shell-seeking crabs. Such physiological and behavioral extremes facilitate a transition to a sheltered lifestyle, revealing the extensive evolutionary lengths that led to their superfamily success. The hermit crabs of Paguroidea are more closely related to squat lobsters and porcelain crabs than they are to true crabs ( Brachyura ). Together with

4002-593: The family Coenobitidae . Two of the most common crabs are the Ecuadorian Hermit crab and the Purple Pincher. The Ecuadorian Hermit Crab (Coenobita compressus) is a grayish black crab that are commonly found in tropical areas as well as beaches and rainforests. They are nocturnal, and are very social. They eat washed up plants, and are recommended they eat mostly plants. They must have seawater close to them, as they need to keep their gills moistened. Overall they are

4089-419: The family Paguridae , have another distinct type of movement. Individuals may crawl upon another's crab shell. If the size is just right the crab climbed upon may move rapidly up and down or sideways, usually causing the other crab to fall off. Anomura Anomura (sometimes Anomala ) is a group of decapod crustaceans , including hermit crabs and others. Although the names of many anomurans include

4176-469: The female moulting, and usually continuing after she has moulted, the male performs precopulatory behaviors. These vary widely but the most common are rotating/shaking the female, and jerking the female towards the male. After some time, the female moves the chelipeds in her mouth region, signaling the male. Then they both move their bodies mostly out of their shells, and mate. Both crabs then go back inside their shells, and they may mate again. In some species

4263-437: The final larval stage, the megalopa . The sexual behavior exhibited by hermit crabs varies from species to species, but a general description is as follows. If the female possesses any larvae from a previous mating, she moults and lets them go. Female hermit crabs are ready to mate shortly before moulting, and she may come in contact with a male. In certain species the male grabs the pre-moult female for sometimes hours. Prior to

4350-459: 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

4437-403: The first two walking legs, or both the first and second pair. This is referred to as "double ambulatory raise", and "quadruple ambulatory raise", respectively. The exact form of this movement is variable between species. In some other species there is another distinct movement, where they move their leg away and upwards from the body, while it moves forwards, this same movement continues as the limb

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4524-402: The genus Pagurus . The second variation called the "cheliped extension", is usually a purely visual movement, though it may sometimes be used to strike a crab. The chelipeds move forward and upwards, until the limb is parallel with the ground, usually used to push another crab out of the way. If a larger crab pushes a smaller one, the smaller one may be moved multiple centimeters. The crabs of

4611-420: The hermit crabs (as they can climb into, but not out of, slippery plastic debris). This can even create a chain reaction of fatality, because a dead hermit crab will release a signal to tell others that a shell is available, luring more hermit crabs to their deaths. More specifically, they are attracted to the scent of dead hermit crab flesh. For some larger marine species, supporting one or more sea anemones on

4698-503: 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

4785-419: The inside of its shell, an aggressive interaction will usually take place, until the defending crab retreats, or the attacker flees. After the defender has retreated, the attacker will usually turn the shell over multiple times, holding it with its legs. It then places its chelipeds into the shell's opening. Then the crabs start the "positioning" behavior, this consists of the attacker moving side to side, over

4872-882: The internal relationships within Anomura are shown in the cladogram below, which shows Hippidae as sister to Paguroidea, and resolves Parapaguridae outside of Paguroidea: Brachyura ("true" crabs) [REDACTED] Porcellanidae (porcelain crabs) [REDACTED] Munididae (squat lobsters) [REDACTED] Parapaguridae (deep water sea anemone hermit crabs) [REDACTED] Eumunididae (squat lobster-like) [REDACTED] Hippidae (mole crabs or sand crabs) [REDACTED] Lithodidae (king crabs) [REDACTED] Paguridae (hermit crabs) [REDACTED] Diogenidae (left-handed hermit crabs) [REDACTED] Coenobitidae (terrestrial hermit crabs) [REDACTED] The infraorder Anomura contained seven extant superfamilies: The oldest fossil attributed to Anomura

4959-634: The larger order Decapoda , from analysis by Wolfe et al. (2019). Dendrobranchiata (prawns) [REDACTED] Stenopodidea (boxer shrimp) [REDACTED] Procarididea Caridea ("true" shrimp) [REDACTED] Achelata (spiny lobsters and slipper lobsters) [REDACTED] Polychelida (benthic crustaceans) Astacidea (lobsters and crayfish) [REDACTED] Axiidea (mud shrimp, ghost shrimp, and burrowing shrimp) Gebiidea (mud lobsters and mud shrimp) [REDACTED] Anomura (hermit crabs and allies) [REDACTED] Brachyura ("true" crabs) [REDACTED] Some of

5046-511: 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

5133-457: The legs and the chelipeds , also known as the claw or pincer. Usually these displays are enough to avoid confrontation. Sometimes two opposing crabs will do multiple actions, with no apparent pattern. These confrontations usually last a few seconds, though some may last a few minutes, for those especially stubborn crabs. They can also raise a leg which is sometimes referred to as an "ambulatory raise". This can happen with multiple legs such as with

5220-427: The living Nautilus ). The earliest ammonoids appeared during the Devonian , with 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

5307-513: The male performs post-copulatory behavior until the female has the eggs on her pleopods . Hermit crabs are omnivorous scavengers that require a varied and balanced diet to thrive. Their dietary needs can be met with a combination of commercial hermit crab food, fresh fruits, vegetables, and occasional treats. A well-rounded diet is essential not only for their general health but also for the proper development of their exoskeleton and overall vitality. High-quality commercial hermit crab food provides

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5394-418: 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 the first saddle and lobe pair past the external region as the suture line extends up

5481-432: 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

5568-533: 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

5655-476: The next size. If the original shell was taken from another hermit crab, the victim is usually left without a shell, and gets eaten. Hermit crabs often "gang up" on one of their species with what they perceive to be a better shell, and pry its shell away from it before competing for it until one takes it over. Aggressive behaviors for hermit crabs are quite similar to one another, with some variations present between species. It usually consists of moving or positioning

5742-436: The ocean to release their larvae, however they cannot submerge themselves in the water as their gills prevent them. Most species have long, spirally curved abdomens , which are soft, unlike the hard, calcified abdomens seen in related crustaceans. The vulnerable abdomen is protected from predators by a salvaged empty seashell carried by the hermit crab, into which its whole body can retract. Most frequently, hermit crabs use

5829-415: The opening of the defender's shell. This movement usually forms a figure 8. The attacker then goes into the aptly named "rapping" behavior. The attacker holds its legs and chepelothorax stationary, while it moves its shell down on the defender's shell. It is done quite rapidly, and is usually enough to produce an audible sound. It seems like little to no contact happens directly between the two crabs. After

5916-472: 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

6003-461: 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

6090-561: The remains of dead animals, providing them with essential nutrients like calcium for their exoskeleton. This diverse diet helps support their health, energy, and successful molting. In addition to commercial food, hermit crabs benefit from a variety of fresh fruits and vegetables. Recommended options include leafy greens such as spinach, as well as carrots, sweet potatoes, and broccoli. Non-citrus fruits like mango, coconut, and papaya can also be offered. These foods provide essential vitamins, minerals, and hydration, which are vital for maintaining

6177-418: 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, the ammonoid suture line (the intersection of the septum with the outer shell) is variably folded, forming saddles ("peaks" that point towards

6264-466: The rock layer in which a particular species or genus is found to specific geologic time periods 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

6351-494: 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

6438-479: 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

6525-518: The shell can scare away predators. The sea anemone also benefits, because it is in a prime position to consume fragments of the hermit crab's meals. Other very close symbiotic relationships are known from encrusting bryozoans and hermit crabs forming bryoliths . In February 2024, Polish researchers reported that 10 of 16 terrestrial hermit crab species were observed using artificial shells, including discarded plastic waste, broken glass bottles and light bulbs, in lieu of natural shells. Shell fighting

6612-415: 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

6699-413: The shell they favour. However, if the crabs vary significantly in size, fights over empty shells are rare. Hermit crabs with undersized shells cannot grow as fast as those with well-fitting shells, and are more likely to be eaten if they cannot retract completely into the shell. Shells used by hermit crabs have usually been remodeled by previous hermit crab owners. This involves a hermit crab hollowing out

6786-722: The shell, making it lighter. Only small hermit crabs are able to live without remodelled shells. Most big hermit crabs that have been transferred to a normal shell die. Even if they were able to survive, hollowing out a shell takes precious energy, making it undesirable to any hermit crab. They achieve this remodeling by both chemically and physically carving out the interiors of their shell. These shells can last for generations, explaining why some hermit crabs are able to live in areas where snails have become locally extinct. There are cases when seashells are not available and hermit crabs will use alternatives such as tin cans, custom-made shells, or any other types of debris, which often proves fatal to

6873-472: The shells of sea snails (although the shells of bivalves and scaphopods and even hollow pieces of wood and stone are used by some species). The tip of the hermit crab's abdomen is adapted to clasp strongly onto the columella of the snail shell. Most hermit crabs are nocturnal . Hermit crab species range in size and shape, from species with a carapace only a few millimetres long to Coenobita brevimanus , which can live 12–70 years and can approach

6960-399: The shells, it is usually eaten. Several hermit crab species, both terrestrial and marine , have been observed forming a vacancy chain to exchange shells. When an individual crab finds a new empty shell, or steals one from another, it will leave its own shell and inspect the vacant shell for size. If the shell is found to be too large, the crab goes back to its own shell and then waits by

7047-548: 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 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

7134-543: 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 the Neo-Latin siphunculus , meaning "little siphon". Originating from within the bactritoid nautiloids, the ammonoid cephalopods first appeared in

7221-446: The size of a coconut. The shell-less hermit crab Birgus latro (coconut crab) is the world's largest terrestrial invertebrate . The young develop in stages, with the first two (the nauplius and protozoea) occurring inside the egg. Most hermit crab larvae hatch at the third stage, the zoea . In this larval stage, the crab has several long spines, a long, narrow abdomen, and large fringed antennae. Several zoeal moults are followed by

7308-486: The squat lobsters and porcelain crabs, they all belong to the infraorder Anomura , the sister taxon to Brachyura. However, the relationship of king crabs to the rest of Paguroidea has been a highly contentious topic. Many studies based on their physical characteristics, genetic information, and combined data demonstrate the longstanding hypothesis that the king crabs in the family Lithodidae are derived hermit crabs descended from pagurids and should be classified as

7395-441: The vacant shell for up to 8 hours. As new crabs arrive they also inspect the shell and, if it is too big, wait with the others, forming a group of up to 20 individuals, holding onto each other in a line from the largest to the smallest crab. As soon as a crab that is the right size for the vacant shell arrives and claims it—leaving its old shell vacant—all the crabs in the queue swiftly exchange shells in sequence, each one moving up to

7482-418: The various groups of anomurans are quite dissimilar. The group has been moulded by several instances of carcinisation – the development of a crab-like body form. Thus, the king crabs (Lithodidae), porcelain crabs (Porcellanidae) and hairy stone crab (Lomisidae) are all separate instances of carcinisation. As decapods (meaning ten-legged ), anomurans have ten pereiopods , but the last pair of these

7569-511: The word crab , all true crabs are in the sister group to the Anomura, the Brachyura (the two groups together form the clade Meiura ). The name Anomura derives from an old classification in which reptant decapods were divided into Macrura (long-tailed), Brachyura (short-tailed) and Anomura (differently-tailed). The alternative name Anomala reflects the unusual variety of forms in this group; whereas all crabs share some obvious similarities,

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