Mollusca
Mollusca Temporal range:
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Tonicella lineata, a polyplacophoran or chiton, anterior end towards the right | |
Scientific classification | |
Kingdom: | |
Superphylum: | |
Phylum: | Mollusca Linnaeus, 1758
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Classes | |
Aplacophora | |
Diversity | |
85,000[1] recognized living species |
Molluscs[note 1] belong to the animal phylum Mollusca. There are around 85,000 recognized extant species, making it the largest marine phylum as it contains about 23% of named marine organisms. Representatives live in marine, freshwater, and terrestrial habitats. Molluscs are highly diverse in size, in anatomical structure, in behaviour and in habitat.
The phylum is typically divided into nine or ten taxonomic classes, of which two are extinct. The gastropods (snails and slugs) include by far the most classified species, accounting for 80% of the total. Cephalopod molluscs such as squid, cuttlefish and octopus are among the most neurologically advanced invertebrates. Either the giant squid or the colossal squid is the largest known invertebrate species.
Molluscs have diverse body structures. The two most universal characteristics are a mantle with a significant cavity used for breathing and excretion, and the structure of the nervous system. As a result, many textbooks base their descriptions on a hypothetical "generalized mollusc", with features common to many, but not all species.
There is good evidence for the appearance of gastropods, cephalopods and bivalves in the Cambrian period 538.8 to 485.4 million years ago. However, the evolutionary history both of molluscs' emergence from the ancestral Lophotrochozoa and of their diversification into the well-known living and fossil forms are still vigorously debated.
There is a risk of food-poisoning from toxins that accumulate in molluscs under certain conditions, and many countries have regulations that aim to minimize this risk. Molluscs have for centuries also been the source of important luxury goods, notably pearls, mother of pearl, Tyrian purple dye, and sea silk. Their shells have also been used as money in some pre-industrial societies.
Mollusc species can also present as hazards or pests to humans. Blue-ringed octopus bites are often fatal, and Octopus apollyon bites can cause inflammation that lasts longer than one month. Stings from a few species of large tropical cone shells can also kill. Their sophisticated though easily-produced venoms have also become important tools in neurological research. Schistosomiasis (also known as bilharzia, bilharziosis or snail fever) is transmitted to humans via water snail hosts, and affects about 200 million people. Snails and slugs can also be serious agricultural pests, and accidental or deliberate introduction of snail species into new environments has seriously damaged some ecosystems.
Diversity
![](http://upload.wikimedia.org/wikipedia/commons/thumb/5/5c/Cypraea_chinensis_with_partially_extended_mantle.jpg/220px-Cypraea_chinensis_with_partially_extended_mantle.jpg)
Estimates of accepted described living species of molluscs vary from 50,000 to maximum 120,000 species.[1] In 2009 Chapman estimated described living 85,000 species.[1] Haszprunar in 2001 estimated about 93,000 named species,[3] which include 23% of all named marine organisms.[4] Molluscs are second only to arthropods in numbers of living animal species[2] – far behind the arthropods' 1,113,000 but well ahead of chordates' 52,000.[5] It has been estimated that there are about 200,000 living species in total,[6][1] and 70,000 fossil species,[7] although the total number of mollusc species that ever existed, whether or not preserved, must be many times greater than the number alive today.[8]
Molluscs have more varied forms than any other animal phylum – snails and other gastropods, clams and other bivalves, squids and other cephalopods, and other lesser-known but similarly distinctive sub-groups. The majority of species still live in the oceans, from the seashores to the abyssal zone, but some are significant members of freshwater and terrestrial ecosystems. They are extremely diverse in tropical and temperate regions but can be found at all latitudes.[9] About 80% of all known mollusc species are gastropods.[2] Cephalopoda such as squid, cuttlefish and octopus are among the most neurologically-advanced of all invertebrates.[10] The giant squid, which until recently had not been observed alive in its adult form,[11] is one of the largest invertebrates. However a recently-caught specimen of the colossal squid, 10 metres (33 ft) long and weighing 500 kilograms (0.49 long tons; 0.55 short tons), may have overtaken it.[12]
Freshwater and terrestrial molluscs appear exceptionally vulnerable to extinction. Estimates of the numbers of non-marine molluscs vary widely, partly because many regions have not been thoroughly surveyed and there is a shortage of specialists in classifying these animals. However, in 2004 the IUCN Red List of Threatened Species included nearly 2,000 endangered non-marine molluscs. For comparison, the great majority of molluscs species are marine but only 41 of these appeared on the 2004 Red List. 42% of recorded extinctions since 1500 involved molluscs, almost entirely non-marine.[13]
Definition
The word mollusc is derived from the French mollusque, which originated from the Latin molluscus, from mollis, soft. Molluscus was itself an adaptation of Aristotle's τᾲ μαλάκια, "the soft things", which he applied to cuttlefish.[14] The scientific study of molluscs is known as malacology.[15]
Molluscs have developed such a varied range of body structures that it is difficult to find synapomorphies (defining characteristics) that apply to all modern groups.[9] The following are present in all modern molluscs:[5][7]
- The dorsal part of the body wall is a mantle which secretes calcareous spicules, plates or shells. It overlaps the body with enough spare room to form a mantle cavity.
- The anus and genitals open into the mantle cavity.
- There are at least two pairs of main nerve cords (three in bivalves[5]: 367–403 )
Other characteristics that commonly appear in textbooks have significant exceptions:
Class | |||||||
Characteristic[7] | Aplacophora[5]: 291–292 | Polyplacophora[5]: 292–298 | Monoplacophora[5]: 298–300 | Gastropoda[16] | Cephalopoda[17] | Bivalvia[18] | Scaphopoda[19] |
---|---|---|---|---|---|---|---|
Radula, a rasping "tongue" with chitinous teeth | Absent in 20% of Neomeniomorpha | Yes | Yes | Yes | Yes | No | Internal, cannot extend beyond body |
Broad, muscular foot | Reduced or absent | Yes | Yes | Yes | Modified into arms | Yes | Small, only at "front" end |
Dorsal concentration of internal organs (visceral mass) | Not obvious | Yes | Yes | Yes | Yes | Yes | Yes |
Large digestive ceca | No ceca in some aplacophora | Yes | Yes | Yes | Yes | Yes | No |
Large complex metanephridia ("kidneys") | None | Yes | Yes | Yes | Yes | Yes | Small, simple |
A "generalized mollusc"
Template:Annotated image/Mollusc generalized Because of the enormous variations between groups of molluscs, many text books start the subject by describing a "generalized mollusc", which some suggest may resemble very early molluscs and which is rather similar to modern monoplacophorans.[9][20][21][22]
The generalized mollusc has a single, "limpet-like" shell on top. The shell is secreted by a mantle that covers the upper surface. The underside consists of a single muscular "foot".[20]
Mantle and mantle cavity
The mantle cavity is a fold in the mantle that encloses a significant amount of space. The cavity was probably at the rear in the earliest molluscs but its position now varies from group to group. The anus, a pair of osphradia (chemical sensors) in the incoming "lane", the hindmost pair of gills and the exit openings of the nephridia ("kidneys") and gonads (reproductive organs) are in the mantle cavity.[20]
Shell
The mantle secretes a shell that is mainly chitin and conchiolin (a protein) hardened with calcium carbonate,[20][23] except that the outermost layer is all conchiolin.[20] Molluscs never use phosphate to construct their hard parts,[24] with the questionable exception of Cobcrephora.[25]
Foot
The underside consists of a muscular foot, which has adapted to different purposes in different classes.[26]: 4 The foot carries a pair of statocysts which act as balance sensors. In gastropods, it secretes mucus as a lubricant to aid movement. In forms that have only a top shell, such as limpets, the foot acts as a sucker attaching the animal to a hard surface, and the vertical muscles clamp the shell down over it; in other molluscs, the vertical muscles pull the foot and other exposed soft parts into the shell.[20] In bivalves, the foot is adapted for burrowing into the sediment;[26]: 4 in cephalopods it is used for jet propulsion,[26]: 4 and the tentacles and arms are derived from the foot.[27]
Multiple functions of organs
Molluscs organs are used for multiple functions. For example: the heart and nephridia ("kidneys") are important parts of the reproductive system as well as the circulatory and excretory systems; in bivalves, the gills both "breathe" and produce a water current in the mantle cavity which serves both excretion and reproduction.
Circulation
Molluscs' circulatory systems are mainly open. Although molluscs are coelomates, their coeloms are reduced to fairly small spaces enclosing the heart and gonads. The main body cavity is a hemocoel through which blood circulates and which encloses most of the other internal organs. The blood contains the respiratory pigment hemocyanin as an oxygen-carrier. The heart consists of one or more pairs of atria (auricles) which receive oxygenated blood from the gills and pump it to the ventricle, which pumps it into the aorta (main artery), which is fairly short and opens into the hemocoel.[20]
The atria of the heart also function as part of the excretory system by filtering waste products out of the blood and dumping it into the coleom as urine. A pair of nephridia ("little kidneys") to the rear of and connected to the coelom extracts any re-usable materials from the urine and dumps additional waste products into it, and then ejects it via tubes that discharge into the mantle cavity.[20]
Respiration
Most molluscs have only one pair of gills, or even only one gill. Generally the gills are rather like feathers in shape, although some species have gills with filaments on only one side. They divide the mantle cavity so that water enters near the bottom and exits near the top. Their filaments have three kinds of cilia, one of which drives the water current through the mantle cavity, while the other two help to keep the gills clean. If the osphradia detect noxious chemicals or possibly sediment entering the mantle cavity, the gills' cilia may stop beating until the unwelcome intrusions have ceased. Each gill has an incoming blood vessel connected to the hemocoel and an outgoing one to the heart.[20]
Eating, digestion, and elimination
![](http://upload.wikimedia.org/wikipedia/commons/thumb/1/19/Snail_radula_working.png/220px-Snail_radula_working.png)
= Food = Radula
= Muscles
= Odontophore "belt"
Most molluscs have muscular mouths with radulae, "tongues" bearing many rows of chitinous teeth, which are replaced from the rear as they wear out. The radula primarily functions to scrape bacteria and algae off rocks. Molluscs mouths also contain glands that secrete slimy mucus, to which the food sticks. Beating cilia (tiny "hairs") drive the mucus towards the stomach, so that the mucus forms a long string.[20]
At the tapered rear end of the stomach and projecting slightly into the hindgut is the prostyle, a backward-pointing cone of feces and mucus, which is rotated by further cilia so that it acts as a bobbin, winding the mucus string onto itself. Before the mucus string reaches the prostyle, the acidity of the stomach makes the mucus less sticky and frees particles from it.[20]
The particles are sorted by yet another group of cilia, which send the smaller particles, mainly minerals, to the prostyle so that eventually they are excreted, while the larger ones, mainly food, are sent to the stomach's cecum (a pouch with no other exit) to be digested. The sorting process is by no means perfect.[20]
Periodically, circular muscles at the hindgut's entrance pinch off and excrete a piece of the prostyle, preventing the prostyle from growing too large. The anus is in the part of the mantle cavity that is swept by the outgoing "lane" of the current created by the gills. Carnivorous molluscs usually have simpler digestive systems.[20]
Nervous system
Molluscs have two pairs of main nerve cords (three in bivalves) the visceral cords serving the internal organs and the pedal ones serving the foot. Both pairs run below the level of the gut, and include ganglia as local control centers in important parts of the body. Most pairs of corresponding ganglia on both sides of the body are linked by commissures (relatively large bundles of nerves). The only ganglia above the gut are the cerebral ganglia, which sit above the esophagus (gullet) and handle "messages" from and to the eyes. The pedal ganglia, which control the foot, are just below the esophagus and their commissure and connections to the cerebral ganglia encircle the esophagus in a nerve ring.[20]
The brain, in species that have one, encircles the esophagus. Most molluscs have a head with eyes, and all have a pair of sensor-containing tentacles, also on the head, that detect chemicals, vibrations and touch.[20]
Reproduction
The simplest molluscan reproductive system relies on external fertilization, but there are more complex variations. All produce eggs, from which may emerge trochophore larvae, more complex veliger larvae, or miniature adults. Two gonads sit next to the coelom that surrounds the heart and shed ova or sperm into the coleom, from which the nephridia extract them and emit them into the mantle cavity. Molluscs that use such a system remain of one sex all their lives and rely on external fertilization. Some molluscs use internal fertilization and/or are hermaphrodites, functioning as both sexes; both of these methods require more complex reproductive systems.[20]
The most basic molluscan larva is a trochophore which is planktonic and feeds on floating food particles by using the two bands of cilia round its "equator" to sweep food into the mouth, which uses more cilia to drive them into the stomach, which uses further cilia to expel undigested remains through the anus. New tissue grows in the bands of mesoderm in the interior, so that the apical tuft and anus are pushed further apart as the animal grows. The trochophore stage is often succeeded by a veliger stage in which the prototroch, the "equatorial" band of cilia nearest the apical tuft, develops into the velum ("veil"), a pair of cilia-bearing lobes with which the larva swims. Eventually the larva sinks to the seafloor and metamorphoses into the adult form. Whilst metamorphosis is the usual state in molluscs, the cephalopods differ in exhibiting direct development: the hatchling is a 'miniaturized' form of the adult.[29]
Taxonomy
Opinions vary about the number of classes of molluscs – for example the table below shows eight living classes,[3] and two extinct ones. However some authors combine the Caudofoveata and solenogasters into one class, the Aplacophora.[22][30] Two of the commonly-recognized classes are known only from fossils[2]
Class | Major organisms | Described living species[3] | Distribution |
Caudofoveata[30] | worm-like organisms | 120 | seabed 200–3,000 metres (660–9,840 ft) |
Aplacophora[30] | solenogasters, worm-like organisms | 200 | seabed 200–3,000 metres (660–9,840 ft) |
Polyplacophora[31] | chitons | 1,000 | rocky tidal zone and seabed |
Monoplacophora[21] | limpet-like organisms | 31 | seabed 1,800–7,000 metres (5,900–23,000 ft); one species 200 metres (660 ft) |
Gastropoda[32] | abalone, limpets, conch, nudibranchs, sea hares, sea butterfly, snails, slugs | 70,000 | marine, freshwater, land |
Cephalopoda[33] | squid, octopus, cuttlefish, nautilus | 900 | marine |
Bivalvia[34] | clams, oysters, scallops, geoducks, mussels | 20,000 | marine, freshwater |
Scaphopoda[19] | tusk shells | 500 | marine 6–7,000 metres (20–22,966 ft) |
Rostroconchia †[35] | fossils; probable ancestors of bivalves | extinct | marine |
Helcionelloida †[36] | fossils; snail-like organisms such as Latouchella | extinct | marine |
Evolution
Fossil record
There is debate about whether some Ediacaran and Early Cambrian fossils really are molluscs. Kimberella, from about 555 million years ago, has been described as "mollusc-like",[37][38] but others are unwilling to go further than "probable bilaterian".[39][note 2][40] There is an even sharper debate about whether Wiwaxia, from about 505 million years ago, was a mollusc, and much of this centers on whether its feeding apparatus was a type of radula or more similar to that of some polychaete worms.[39][41] Nicholas Butterfield, who opposes the idea that Wiwaxia was a mollusc, has written that earlier microfossils from 515 to 510 million years ago are fragments of a genuinely mollusc-like radula.[42]
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However, the Helcionellids, which first appear over 540 million years ago in Early Cambrian rocks from Siberia and China,[43][44] are thought to be early molluscs with rather snail-like shells. Shelled molluscs therefore predate the earliest trilobites.[36] Although most helcionellid fossils are only a few millimeters long, specimens a few centimeters long have also been found, most with more limpet-like shapes. There have been suggestions that the tiny specimens were juveniles and the larger ones adults.[45]
Some analyses of helcionellids concluded that these were the earliest gastropods.[46] However other scientists are not convinced that Early Cambrian fossils show clear signs of the torsion that identifies modern gastropods twists the internal organs so that the anus lies above the head.[16][47][48]
For a long time it was thought that Volborthella, some fossils of which pre-date 530 million years ago, was a cephalopod. However discoveries of more detailed fossils showed that Volborthella’s shell was not secreted but built from grains of the mineral silicon dioxide (silica), and that it was not divided into a series of compartments by septa as those of fossil shelled cephalopods and the living Nautilus are. Volborthella’s classification is uncertain.[49] The Late Cambrian fossil Plectronoceras is now thought to be the earliest clearly cephalopod fossil, as its shell had septa and a siphuncle, a strand of tissue that Nautilus uses to remove water from compartments that it has vacated as it grows, and which is also visible in fossil ammonite shells. However, Plectronoceras and other early cephalopods crept along the seafloor instead of swimming, as their shells contained a "ballast" of stony deposits on what is thought to be the underside and had stripes and blotches on what is thought to be the upper surface.[50] All cephalopods with external shells except the nautiloids became extinct by the end of the Cretaceous period 65 million years ago.[51] However, the shell-less Coleoidea (squid, octopus, cuttlefish) are abundant today.[52]
The Early Cambrian fossils Fordilla and Pojetaia are regarded as bivalves.[53][54][55][56] "Modern-looking" bivalves appeared in the Ordovician period, 488 to 443 million years ago.[57] One bivalve group, the rudists, became major reef-builders in the Cretaceous, but became extinct in the Cretaceous-Tertiary extinction.[58] However, bivalves are now abundant and diverse.
Phylogeny
Lophotrochozoa |
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The phylogeny (evolutionary "family tree") of molluscs is a controversial subject. In addition to the debates about whether Kimberella and any of the "halwaxiids" were molluscs or closely related to molluscs,[38][39][41][42] there are debates about the relationships between the classes of living molluscs.[40] In fact some groups traditionally classifed as molluscs may have to be redefined as distinct but related.[61]
Molluscs are generally regarded members of the Lophotrochozoa,[59] a group defined by having trochophore larvae and, in the case of living Lophorata, a feeding structure called a lophophore. The other members of the Lophotrochozoa are the annelid worms and seven marine phyla.[62] The diagram on the right summarizes a phylogeny presented in 2007.
Because the relationships between the members of the family tree are uncertain, it difficult to identify the features inherited from the last common ancestor of all molluscs.[63] For example it is uncertain whether the ancestral mollusc was metameric (composed of repeating units) - if it was, that would suggest an origin from an annelid-like worm.[64] Scientists disagree about this: Giribet and colleagues concluded in 2006 that the repetition of gills and of the foot's retractor muscles were later developments, [9] while in 2007 Sigwart concluded that the ancestral mollusc was metameric, and that it had a foot used for creeping and a "shell" that was mineralized.[40] In one particular one branch of the family tree, the shell of conchiferans is thought to have evolved from the spicules (small spines) of aplacophorans; however this is difficult to reconcile with the embryological origins of spicules.[63]
The molluscan shell appears to have originated from a mucus coating, which eventually stiffened into a cuticle. This would have been impermeable and thus forced the development of more sophisticated respiratory apparatus in the form of gills.[36] Eventually, the cuticle would have become mineralized,[36] using the same genetic machinery (engrailed) as most other bilaterian skeletons.[64] The first mollusc shell almost certainly was reinforced with the mineral aragonite.[65]
The evolutionary relationships within the molluscs are also debated, and the diagrams below show two widely-supported reconstructions:
However, an analysis in 2009 that used both morphological and molecular phylogenetics comparisons concluded that the molluscs are not monophyletic; in particular, that Scaphopoda and Bivalvia are both separate, monophyletic lineages unrelated to the remaining molluscan classes – in other words that the traditional phylum Mollusca is polyphyletic, and that it can only be made monophyletic if scaphopods and bivalves are excluded.[61] A 2010 analysis similarly concluded that the molluscs are not monophyletic, this time suggesting that solenogastres are more closely related to the non-molluscan taxa used as an outgroup than to other molluscs.[66]
Relations with humans
Uses by humans
Molluscs, especially bivalves such as clams and mussels, have been an important food source since at least the advent of anatomically modern humans – and this has often resulted in over-fishing.[67] Other commonly eaten molluscs include octopuses and squids, whelks, oysters, and scallops.[68] In 2005, China accounted for 80% of the global mollusc catch, netting almost 11,000,000 tonnes (11,000,000 long tons; 12,000,000 short tons). Within Europe, France remained the industry leader.[69] Some countries regulate importation and handling of molluscs and other seafood, mainly to minimize the poison risk from toxins that accumulate in the animals.[70]
![Photo of three circular metal cages in shallows, with docks, boathouses and palm trees in background](http://upload.wikimedia.org/wikipedia/commons/thumb/d/d8/Pearl_farm_%28Seram%2C_Indonesia%29.jpg/200px-Pearl_farm_%28Seram%2C_Indonesia%29.jpg)
Most molluscs that have shells can produce pearls, but only the pearls of bivalves and some gastropods whose shells are lined with nacre are valuable.[16][18] The best natural pearls are produced by pearl oyster.s Pinctada margaritifera and Pinctada mertensi, which live in the tropical and sub-tropical waters of the Pacific Ocean. Natural pearls form when a small foreign object gets stuck between the mantle and shell.
There are two methods of culturing pearls, by inserting either "seeds" or beads into oysters. The "seed" method uses grains of ground shell from freshwater mussels, and over-harvesting for this purpose has endangered several freshwater mussel species in the southeastern USA.[18] The pearl industry is so important in some areas that significant sums of money are spent on monitoring the health of farmed molluscs.[71]
![Mosaic of mustachioed, curly-haired man wearing crown and surrounded by halo](http://upload.wikimedia.org/wikipedia/commons/thumb/8/89/Meister_von_San_Vitale_in_Ravenna.jpg/100px-Meister_von_San_Vitale_in_Ravenna.jpg)
Other luxury and high-status products were made from molluscs. Tyrian purple, made from the ink glands of murex shells, "... fetched its weight in silver" in the fourth-century BC, according to Theopompus.[72] The discovery of large numbers of Murex shells on Crete suggests that the Minoans may have pioneered the extraction of "Imperial purple" during the Middle Minoan period in the 20th–18th century BC, centuries before the Tyrians.[73][74] Sea silk is a fine, rare and valuable fabric produced from the long silky threads (byssus) secreted by several bivalve molluscs, particularly Pinna nobilis, to attach themselves to the sea bed.[75] Procopius, writing on the Persian wars circa 550 CE, "stated that the five hereditary satraps (governors) of Armenia who received their insignia from the Roman Emperor were given chlamys (or cloaks) made from lana pinna (Pinna "wool," or byssus). Apparently only the ruling classes were allowed to wear these chlamys."[76]
Mollusc shells, including those of cowries, were used as a kind of money in several pre-industrial societies. However these "currencies" generally differed in important ways from the standardized government-backed and -controlled money familiar to industrial societies. Some shell "currencies" were not used for commercial transactions but mainly as social status displays at important occasions such as weddings.[77] When used for commercial transactions they functioned as commodity money, in other words as a tradable commodity whose value differed from place to place, often as a result of difficulties in transport, and which was vulnerable to incurable inflation if more efficient transport or "goldrush" behavior appeared.[78]
Threats to humans
Stings and bites
When handled alive, a few species of molluscs can sting or bite and, with some species, this can present a serious risk to the human handling the animal. To put this into perspective however, deaths from mollusc venoms are less than 10% of the number of deaths from jellyfish stings.[80]
All octopuses are venomous[81] but only a few species pose a significant threat to humans. Blue-ringed octopuses in the genus Hapalochlaena, which live around Australia and New Guinea, bite humans only if severely provoked,[79] but their venom kills 25% of human victims. Another tropical species, Octopus apollyon, causes severe inflammation that can last for over a month even if treated correctly.[82]
Cone snails, carnivorous gastropods that feed on marine invertebrates (and in the case of larger species on fish), produce a huge array of toxins, some fast-acting and others slower but deadlier – they can afford to do this because their toxins require less time and energy to be produced compared with those of snakes or spiders.[83] Many painful stings have been reported and a few fatalities, although some of the reported fatalities may be exaggerations.[80] Only the few larger species of cone snail that can capture and kill fish are likely to be seriously dangerous to humans.[84] The effects of individual cone shell toxins on victims' nervous systems are so precise that they are useful tools for research in neurology, and the small size of their molecules makes it easy to synthesize them.[83][85]
The traditional belief that a giant clam can trap the leg of a person between its valves, thus drowning them, is a myth.[86]
Pests
![](http://upload.wikimedia.org/wikipedia/commons/thumb/2/27/Schistosomiasis_itch.jpeg/220px-Schistosomiasis_itch.jpeg)
Schistosomiasis (also known as bilharzia, bilharziosis or snail fever) is "second only to malaria as the most devastating parasitic disease in tropical countries. An estimated 200 million people in 74 countries are infected with the disease — 100 million in Africa alone."[87] The parasite has 13 known species, of which two infect humans. The parasite itself is not a mollusc, but all the species have freshwater snails as intermediate hosts.[88]
Some species of molluscs, particularly certain snails and slugs, can be serious crop pests,[89] and when introduced into new environments can unbalance local ecosystems. One such pest, the giant African snail Achatina fulica, has been introduced to many parts of Asia, as well as to many islands in the Indian Ocean and Pacific Ocean. In the 1990s this species reached the West Indies. Attempts to control it by introducing the predatory snail Euglandina rosea proved disastrous, as the predator ignored Achatina fulica and went on to extirpate several native snail species instead.[90]
Despite its name, Molluscum contagiosum is a viral disease, and is unrelated to molluscs.[91]
Notes
References
- ^ a b c d Chapman, A.D. (2009). Numbers of Living Species in Australia and the World, 2nd edition. Australian Biological Resources Study, Canberra. Accessed 12 January 2010. ISBN 978 0 642 56860 1 (printed); ISBN 978 0 642 56861 8 (online).
- ^ a b c d edited by Winston F. Ponder, David R. Lindberg. (2008). Ponder, W.F. and Lindberg, D.R. (ed.). Phylogeny and Evolution of the Mollusca. Berkeley: University of California Press. p. 481. ISBN 978-0520250925.
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has generic name (help)CS1 maint: multiple names: editors list (link) - ^ a b c Haszprunar, G. (2001). "Mollusca (Molluscs)". Encyclopedia of Life Sciences. John Wiley & Sons, Ltd. doi:10.1038/npg.els.0001598.
- ^ Rebecca Hancock (2008). "Recognising research on molluscs". Australian Museum. Retrieved 2009-03-09.
- ^ a b c d e f Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. p. Front endpaper. ISBN 0030259827.
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: CS1 maint: multiple names: authors list (link) - ^ Winston F. Ponder and David R. Lindberg (2004). "Phylogeny of the Molluscs". World Congress of Malacology. Retrieved 2009-03-09.
- ^ a b c Brusca, R.C., and Brusca, G.J. (2003). Invertebrates (2 ed.). Sinauer Associates. p. 702. ISBN 0878930973.
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: CS1 maint: multiple names: authors list (link) - ^ David M. Raup & Steven M. Stanley (1978). Principles of Paleontology (2 ed.). W.H. Freeman and Co. pp. 4–5. ISBN 071670220.
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value: length (help) - ^ a b c d Giribet, G., Okusu, A., Lindgren, A.R., Huff, S.W., Schrödl, M., and Nishiguchi, M.K. (May 2006). "Evidence for a clade composed of molluscs with serially repeated structures: Monoplacophorans are related to chitons". Proceedings of the National Academy of Sciences of the United States of America. 103 (20): 7723–7728. doi:10.1073/pnas.0602578103. PMC 1472512. PMID 16675549. Retrieved 2008-09-30.
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: CS1 maint: multiple names: authors list (link) - ^ Barnes, R.S.K., Calow, P., Olive, P.J.W., Golding, D.W. and Spicer, J.I. (2001). The Invertebrates, A Synthesis (3 ed.). UK: Blackwell Science.
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: CS1 maint: multiple names: authors list (link) - ^ Kubodera, T. and Mori, K. date=2005 (2005). "First-ever observations of a live giant squid in the wild" (PDF). Proceedings of the Royal Society B: Biological Sciences. 272 (1581): 2583–2586. doi:10.1098/rspb.2005.3158. Retrieved 2008-10-22.
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- ^ Lydeard, C. (April 2004). "The global decline of nonmarine mollusks" (PDF). BioScience. 54: 321–330. doi:10.1641/0006-3568(2004)054[0321:TGDONM]2.0.CO;2. Retrieved 20 Oct 2009.
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: CS1 maint: multiple names: editors list (link) - ^ a b c d Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. pp. 300–343. ISBN 0030259827.
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: CS1 maint: multiple names: authors list (link) - ^ Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. pp. 343–367. ISBN 0030259827.
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: CS1 maint: multiple names: authors list (link) - ^ a b Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. pp. 403–407. ISBN 0030259827.
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- ^ Porter, S. (2007). "Seawater Chemistry and Early Carbonate Biomineralization". Science. 316 (5829): 1302. doi:10.1126/science.1137284. PMID 17540895. Retrieved 2008-09-30.
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|doi=10.1144/gsjgs.131.6.0661
instead. - ^ Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1080/00241160410002180, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with
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- ^ Shigeno, S; Sasaki, T; Moritaki, T; Kasugai, T; Vecchione, M; Agata, K (2008). "Evolution of the cephalopod head complex by assembly of multiple molluscan body parts: Evidence from Nautilus embryonic development". Journal of morphology. 269 (1): 1–17. doi:10.1002/jmor.10564. PMID 17654542.
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ignored (help)CS1 maint: multiple names: authors list (link) - ^ Ruppert, E.E.; Fox, R.S. & Barnes, R.D. (2004). "Mollusca". Invertebrate Zoology (7th ed.). Brooks / Cole. pp. 290–291. ISBN 0030259827.
- ^ Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1016/j.crpv.2004.07.009, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with
|doi=10.1016/j.crpv.2004.07.009
instead. - ^ a b c Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. pp. 291–292. ISBN 0030259827.
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: CS1 maint: multiple names: authors list (link) - ^ Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. p. 300. ISBN 0030259827.
{{cite book}}
: CS1 maint: multiple names: authors list (link) - ^ Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. p. 343. ISBN 0030259827.
{{cite book}}
: CS1 maint: multiple names: authors list (link) - ^ Ruppert, E.E., Fox, R.S., and Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. p. 367. ISBN 0030259827.
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: CS1 maint: multiple names: authors list (link) - ^ Clarkson, E.N.K., (1998). Invertebrate Palaeontology and Evolution. Blackwell. p. 221. ISBN 0632052384. Retrieved 2008-10-27.
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: CS1 maint: extra punctuation (link) CS1 maint: multiple names: authors list (link) - ^ a b c d e Runnegar, B. and Pojeta, J. (1974). "Molluscan phylogeny: the paleontological viewpoint". Science. 186 (4161): 311–7. doi:10.1126/science.186.4161.311. PMID 17839855. Retrieved 2008-07-30.
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: CS1 maint: multiple names: authors list (link) - ^ Fedonkin, M.A. (1997). "The Late Precambrian fossil Kimberella is a mollusc-like bilaterian organism". Nature. 388 (6645): 868. doi:10.1038/42242.
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suggested) (help) - ^ a b Fedonkin, M.A., Simonetta, A. and Ivantsov, A.Y. (2007). "New data on Kimberella, the Vendian mollusc-like organism (White Sea region, Russia): palaeoecological and evolutionary implications" (PDF). Geological Society, London, Special Publications. 286: 157–179. doi:10.1144/SP286.12. Retrieved 2008-07-10.
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: CS1 maint: multiple names: authors list (link) - ^ a b c Butterfield, N.J. (2006). "Hooking some stem-group "worms": fossil lophotrochozoans in the Burgess Shale". Bioessays. 28 (12): 1161–6. doi:10.1002/bies.20507. PMID 17120226.
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:|access-date=
requires|url=
(help) - ^ a b c Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1098/rspb.2007.0701, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with
|doi=10.1098/rspb.2007.0701
instead. - ^ a b Caron, J.B. (2006-07-13). "A soft-bodied mollusc with radula from the Middle Cambrian Burgess Shale" (PDF). Nature. 442 (7099): 159–163. doi:10.1038/nature04894. PMID 16838013. Retrieved 2008-08-07.
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- ^ P. Yu. Parkhaev (2007). "The Cambrian 'basement' of gastropod evolution". Geological Society, London, Special Publications. 286: 415–421. doi:10.1144/SP286.31. Retrieved 2009-11-01.
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: CS1 maint: multiple names: authors list (link) - ^ Mus, M. M.; Palacios, T.; Jensen, S. (2008). "Size of the earliest mollusks: Did small helcionellids grow to become large adults?". Geology. 36 (2): 175. doi:10.1130/G24218A.1. Retrieved 2008-10-01.
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: CS1 maint: multiple names: authors list (link) - ^ Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1666/0022-3360(2002)076<0287:LECSSF>2.0.CO;2, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with
|doi=10.1666/0022-3360(2002)076<0287:LECSSF>2.0.CO;2
instead. - ^ Frýda, J. (2008). "Paleozoic Gastropoda". In Ponder, W.F., and Lindberg, D.R. (ed.). Phylogeny and evolution of the Mollusca. California Press. pp. 239–264. ISBN 0520250923. Retrieved 4 Nov 2009.
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suggested) (help)CS1 maint: multiple names: editors list (link) - ^ Kouchinsky, A. (2000). "Shell microstructures in Early Cambrian molluscs" (PDF). Acta Palaeontologica Polonica. 45 (2): 119–150. Retrieved 4 Nov 2009.
- ^ Hagadorn, J.W., and Waggoner, B.M. (2002). "The Early Cambrian problematic fossil Volborthella: New insights from the Basin and Range". In Corsetti, F.A. (ed.). Proterozoic-Cambrian of the Great Basin and Beyond, Pacific Section SEPM Book 93 (PDF). SEPM (Society for Sedimentary Geology). pp. 135–150. Retrieved 2008-10-01.
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: CS1 maint: multiple names: authors list (link) - ^ Vickers-Rich, P., Fenton, C.L., Fenton, M.A. and Rich, T.H. (1997). The Fossil Book: A Record of Prehistoric Life. Courier Dover Publications. pp. 269–272. ISBN 0486293718.
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: CS1 maint: multiple names: authors list (link) - ^ Marshall C.R., and Ward P.D. (1996). "Sudden and Gradual Molluscan Extinctions in the Latest Cretaceous of Western European Tethys". Science. 274 (5291): 1360–1363. doi:10.1126/science.274.5291.1360. PMID 8910273.
- ^ Monks, N. "A Broad Brush History of the Cephalopoda". Retrieved 2009-03-21.
- ^ Pojeta, J. (2000). "Cambran Pelecypoda (Mollusca)". American Malacological Bulletin. 15: 157–166.
- ^ Schneider, J.A. (November 2001). "Bivalve systematics during the 20th century". Journal of Paleontology. 75 (6): 1119–1127. doi:10.1666/0022-3360(2001)075<1119:BSDTC>2.0.CO;2. Retrieved 2008-10-05.
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: CS1 maint: date and year (link) - ^ Gubanov, A.P., Kouchinsky, A.V. and Peel, J.S. "The first evolutionary-adaptive lineage within fossil molluscs". Lethaia. 32 (2): 155–157.
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: CS1 maint: multiple names: authors list (link) - ^ Gubanov, A.P., and Peel, J.S. (2003). "The early Cambrian helcionelloid mollusc Anabarella Vostokova". Palaeontology. 46 (5): 1073–1087. doi:10.1111/1475-4983.00334.
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: CS1 maint: multiple names: authors list (link) - ^ Zong-Jie, F. (2006). "An introduction to Ordovician bivalves of southern China, with a discussion of the early evolution of the Bivalvia". Geological Journal. 41 (3–4): 303–328. doi:10.1002/gj.1048.
- ^ Raup, D.M., and Jablonski, D. (1993). "Geography of end-Cretaceous marine bivalve extinctions". Science. 260 (5110): 971–973. doi:10.1126/science.11537491. PMID 11537491.
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: CS1 maint: multiple names: authors list (link) - ^ a b c d e Sigwart, J.D., and Sutton, M.D. (October 2007). "Deep molluscan phylogeny: synthesis of palaeontological and neontological data". Proceedings of the Royal Society: Biology. 274 (1624): 2413–2419. doi:10.1098/rspb.2007.0701. PMC 2274978.
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: CS1 maint: multiple names: authors list (link) For a summary, see "The Mollusca". University of California Museum of Paleontology. Retrieved 2008-10-02. - ^ "The Mollusca". University of California Museum of Paleontology. Retrieved 2008-10-02.
- ^ a b Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1111/j.1096-0031.2009.00255.x
, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with
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instead. - ^ "Introduction to the Lophotrochozoa". University of California Museum of Paleontology. Retrieved 2008-10-02.
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|doi=10.1016/j.ydbio.2004.04.027
instead. - ^ a b Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1046/j.1525-142x.2000.00077.x, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with
|doi=10.1046/j.1525-142x.2000.00077.x
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|doi=10.1126/science.1137284
instead. - ^ Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1016/j.ympev.2009.07.028, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with
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instead. - ^ Mannino, M.A., and Thomas, K.D. (February 2002). "Depletion of a resource? The impact of prehistoric human foraging on intertidal mollusc communities and its significance for human settlement, mobility and dispersal". World Archaeology. 33 (3): 452–474. doi:10.1080/00438240120107477.
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: CS1 maint: multiple names: authors list (link) - ^ Garrow, J.S., Ralph, A., and James, W.P.T. (2000). Human Nutrition and Dietetics. Elsevier Health Sciences. p. 370. ISBN 0443056277.
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: CS1 maint: multiple names: authors list (link) - ^ "China catches almost 11 m tonnes of molluscs in 2005". FAO. Retrieved 2008-10-03.
- ^ "Importing fishery products or bivalve molluscs". United Kingdom: Food Standards Agency. Retrieved 2008-10-02.
- ^ Jones, J.B., and Creeper, J. (April 2006). "Diseases of Pearl Oysters and Other Molluscs: a Western Australian Perspective". Journal of Shellfish Research. 25 (1): 233–238. doi:10.2983/0730-8000(2006)25[233:DOPOAO]2.0.CO;2.
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: CS1 maint: date and year (link) CS1 maint: multiple names: authors list (link) - ^ The fourth-century BC historian Theopompus, cited by Athenaeus (12:526) around 200 BC ; according to Gulick, C.B. (1941). Athenaeus, The Deipnosophists. Cambridge, Mass.: Harvard University Press.
- ^ Reese, D.S. (1987). "Palaikastro Shells and Bronze Age Purple-Dye Production in the Mediterranean Basin". Annual of the British School of Archaeology at Athens. 82: 201–6.
- ^ Stieglitz, R.R. (1994). "The Minoan Origin of Tyrian Purple". Biblical Archaeologist. 57: 46–54. doi:10.2307/3210395.
- ^ Webster's Third New International Dictionary (Unabridged) 1976. G. & C. Merriam Co., p. 307.
- ^ Turner, R.D., and Rosewater, J. (June 1958). "The Family Pinnidae in the Western Atlantic". Johnsonia. 3 (38): 294.
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: CS1 maint: multiple names: authors list (link) - ^ Maurer, B. (October 2006). "The Anthropology of Money" (PDF). Annual Review of Anthropology. 35: 15–36. doi:10.1146/annurev.anthro.35.081705.123127. Retrieved 2008-10-23.
- ^ Hogendorn, J., and Johnson, M. (2003). The Shell Money of the Slave Trade. Cambridge University Press. ISBN 052154110.
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value: length (help)CS1 maint: multiple names: authors list (link) Particularly chapters "Boom and slump for the cowrie trade" (pages 64-79) and "The cowrie as money: transport costs, values and inflation" (pages 125-147) - ^ a b Alafaci, A. "Blue ringed octopus". Australian Venom Research Unit. Retrieved 2008-10-03.
- ^ a b Williamson, J.A., Fenner, P.J., Burnett, J.W., and Rifkin, J. (1996). Venomous and Poisonous Marine Animals: A Medical and Biological Handbook. UNSW Press. pp. 65–68. ISBN 0868402796. Retrieved 2008-10-03.
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: CS1 maint: multiple names: authors list (link) - ^ Anderson, R.C. (1995) Aquarium husbandry of the giant Pacific octopus. Drum and Croaker 26:14-23
- ^ Brazzelli, V., Baldini, F., Nolli, G., Borghini, F., and Borroni, G. (1999). "Octopus apollyon bite". Contact Dermatitis. 40 (3): 169–170. doi:10.1111/j.1600-0536.1999.tb06025.x. PMID 10073455.
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: CS1 maint: multiple names: authors list (link) - ^ a b c Concar, D. (19 October 1996). "Doctor snail – Lethal to fish and sometimes even humans, cone snail venom contains a pharmacopoeia of precision drugs". New Scientist. Retrieved 2008-10-03.
- ^ Livett, B. "Cone Shell Mollusc Poisoning, with Report of a Fatal Case". Department of Biochemistry and Molecular Biology, University of Melbourne.
- ^ Haddad, V.(junior), de Paula Neto, J.B., and Cobo, V.J. (September–October 2006). "Venomous mollusks: the risks of human accidents by Conus snails (Gastropoda: Conidae) in Brazil" (PDF). 39 ((5)): 498–500. Retrieved 2008-10-03.
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: Cite journal requires|journal=
(help); Unknown parameter|journa=
ignored (help)CS1 maint: date format (link) CS1 maint: multiple names: authors list (link) - ^ Cerullo, M.M., Rotman, J.L., and Wertz, M. (2003). The Truth about Dangerous Sea Creatures. Chronicle Books. p. 10. ISBN 0811840506. Retrieved 2008-10-03.
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: CS1 maint: multiple names: authors list (link) - ^ "The Carter Center Schistosomiasis Control Program". The Carter Center. Retrieved 2008-10-03.
- ^ Brown, D.S. (1994). Freshwater Snails of Africa and Their Medical Importance. CRC Press. p. 305. ISBN 0748400265.
- ^ Barker, G.M. (2002). Molluscs As Crop Pests. CABI Publications. ISBN 0851993206.
- ^ Civeyrel, L., and Simberloff, D. (October 1996). "A tale of two snails: is the cure worse than the disease?". Biodiversity and Conservation. 5 (10): 1231–1252. doi:10.1007/BF00051574.
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: CS1 maint: multiple names: authors list (link) - ^ "Molluscum (Molluscum Contagiosum): Frequently Asked Questions for Everyone". Centers for Disease Control and Prevention. Retrieved 2008-10-03.
Further reading
- Starr & Taggart (2002). Biology: The Unity and Diversity of Life. Pacific Grove, California: Thomson Learning.
- Nunn, J.D., Smith, S.M., Picton, B.E. and McGrath, D. 2002. Checklist, atlas of distribution and bibliography for the marine mollusca of Ireland. in hey did u kniow that i like penis dfmnangj
External links
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