Gastropod shell

"Snail shell" redirects here. For the cave in Tennessee, see Snail Shell Cave. For the They Might Be Giants song, see John Henry (album).
Shells of two different species of sea snail: on the left is the normally sinistral (left-handed) shell of Neptunea angulata, on the right is the normally dextral (right-handed) shell of Neptunea despecta
The shell of a large land snail (probably Helix pomatia) with parts broken off to show the interior structure.
1 – umbilicus
2 – columellar plait
3 – aperture
4 – columella
5 – suture
6 – body whorl
7 – apex
Four views of a shell of Arianta arbustorum: Apertural view of (top left), lateral view (top right), apical view (bottom left), and umbilical view (bottom right).

The gastropod shell is part of the body of a gastropod or snail, a kind of mollusk or mollusc. The shell is an external skeleton or exoskeleton, which may serve for muscle attachment, but also for protection from predators, mechanical damage, dehydration, and calcium storage. Some gastropods appear shell-less (slugs) but may have a remnant within the mantle, or the shell is reduced such that the body cannot be retracted within (semi-slug). Some snails also possess an operculum that seals the opening of the shell, known as the aperture, which provides further protection. The study of mollusc shells is known as conchology. The biological study of gastropods, and other molluscs in general, is malacology. Shell morphology terms vary by species group. An excellent source for terminology of the gastropod shell is "How to Know the Eastern Land Snails" by John B. Burch now freely available at the Hathi Trust Digital Library.[1]

Formation of the shell

Main articles: mantle (mollusc), mollusc shell, and nacre

The gastropod shell has three major layers secreted by the mantle. The calcareous central layer, the ostracum, is typically made of calcium carbonate precipitated into an organic matrix known as conchiolin. The outermost layer is the periostracum which is resistant to abrasion and provides most shell coloration. The body of the snail contacts the innermost smooth layer that may be composed of mother-of-pearl or shell nacre, a dense horizontally packed form of conchiolin, which is layered upon the periostracum as the snail grows.


Morphology of typical spirally coiled shell. The shell of Zonitoides nitidus, a land snail, has dextral coiling.

Upper image: Dorsal view, showing whorls and apex
Central image: Lateral view showing the profile of the shell
Lower image: Basal view showing umbilicus in the centre.

Photo of the shell of Zonitoides nitidus with an
apical view, an apertural view and a basal view

Gastropod shell morphology is usually quite constant among individuals of a species. Controlling variables are:

Some of these factors can be modelled mathematically and programs exist to generate extremely realistic images. Early work by David Raup on the analog computer also revealed many possible combinations that were never adopted by any actual gastropod.

Some shell shapes are found more often in certain environments, though there are many exceptions. Wave-washed high-energy environments, such as the rocky intertidal zone, are usually inhabited by snails whose shells have a wide aperture, a relatively low surface area, and a high growth rate per revolution. High-spired and highly sculptured forms become more common in quiet water environments. The shell of burrowing forms, such as the olive and Terebra, are smooth, elongated, and lack elaborate sculpture, in order to decrease resistance when moving through sand. On land, high-spired forms are often associated with vertical surfaces, whereas flat-shelled snails tend to live on the ground.

A few gastropods, for instance the Vermetidae, cement the shell to, and grow along, solid surfaces such as rocks, or other shells.


Most gastropod shells are spirally coiled. The majority (over 90%)[2] of gastropod species have dextral (right-handed) shells, but a small minority of species and genera are virtually always sinistral (left-handed), and a very few species (for example Amphidromus perversus[3]) show a mixture of dextral and sinistral individuals.

If a coiled gastropod shell is held with the spire pointing upwards and the aperture more or less facing the observer, a dextral shell will have the aperture on the right-hand side, and a sinistral shell will have the aperture on the left-hand side. This chirality of gastropods is often overlooked when photographs of coiled gastropods are "flipped" by a non-expert prior to being used in a publication. This image "flipping" results in a normal dextral gastropod appearing to be a rare or abnormal sinistral one.

The chirality in gastropods appears in early cleavage (spiral cleavage) and the gene NODAL is involved.[4] A more recent study (2013) correlates the asymmetric coiling of the shell by the left-right asymmetric expression of the decapentaplegic gene in the mantle.[5]

Mixed coiling populations

In few cases, both left- and right-handed coiling are found in the same population.[6] Sinistral mutants of normally dextral species and dextral mutants of normally sinistral species are rare but well documented occurrences among land snails in general.[6] Populations or species with normally mixed coiling are much rarer, and, so far as is known, are confined, with one exception, to a few genera of arboreal tropical snails.[6] Besides Amphidromus, the Cuban Liguus vittatus (Swainson), Haitian Liguus virgineus (Linnaeus) (family Orthalicidae), some Hawaiian Partulina and many Hawaiian Achatinella (family Achatinellidae), as well as several species of Pacific islands Partula (family Partulidae), are known to have mixed dextral-sinistral populations.[6]

A possible exception may concern some of the European clausiliids of the subfamily Alopiinae.[6] They are obligatory calciphiles living in isolated colonies on limestone outcrops.[6] Several sets of species differ only in the direction of coiling, but the evidence is inconclusive as to whether left- and right-handed shells live together.[6] Soos (1928, pp. 372–385) summarized previous discussions of the problem and concluded that the right- and left-handed populations were distinct species.[6] Others have stated that these populations were not distinct, and the question is far from settled.[6] The Peruvian clausiliid, Nenia callistoglypta Pilsbry (1949, pp. 216–217), also has been described as being an amphidromine species.[6]

The genetics of reverse coiling in a rare dextral mutant of another clausiliid, Alinda biplicata (Montagu), has been studied by Degner (1952).[6] The mechanism is the same as in Radix peregra (Müller), with the direction of coiling determined by a simple Mendelian recessive.[6]

Standard ways of viewing a shell

In photographs or illustrations, a gastropod shell can be shown oriented in a number of standard ways:


The shell begins with the minute embryonic whorls of the protoconch, which is often quite distinct from the rest of the shell. From the protoconch, which forms the apex of the spire, the coils or whorls of the shell gradually increase in size. Normally the whorls are circular or elliptical in section, but from compression and other causes a variety of forms can result. The spire can be high or low, broad or slender according to the way the coils of the shell are arranged, and the apical angle of the shell varies accordingly. The whorls sometimes rest loosely upon one another (as in Epitonium scalare). They also can overlap the earlier whorls such that they may be largely or wholly covered by the later ones. When an angulation occurs, the space between it and the suture above it constitutes the area known as the "shoulder" of the shell. The shoulder angle may be simple or keeled, and may sometimes have nodes or spines.

The most primitive sculpture of the gastropod shell consists of revolving ridges or spirals, and of transverse folds or ribs. Primary spirals appear in regular succession on either side of the first primary, which generally becomes the shoulder angle if angulation occurs. Secondary spirals appear by intercalation between the primary ones, and generally are absent in the young shell, except in some highly accelerated types. Tertiary spirals are intercalated between the preceding groups in more specialized species. Ribs are regular transverse foldings of the shell, which generally extend from the suture to suture. They are usually spaced uniformly and crossed by the spirals. In specialized types, when a shoulder angle is formed, they become concentrated as nodes upon this angle, disappearing from the shoulder above and the body below. Spines may replace the nodes in later stages. They form as notches in the margin of the shell and are subsequently abandoned, often remaining open in front. Irregular spines may also arise on various parts of the surface of the shell (see Platyceras). When a row of spines is formed at the edge or outer lip of the shell this sometimes remains behind as a varix as in (Murex) and many of the Ranellidae. Varices may also be formed by simple expansion of the outer lip, and a subsequent resumption of growth from the base of the expansion. These simple varices may project from the shell (Epitonium) or be reflected backwards (Harpa). Periodic enlargements of ribs are not considered as varices.

The aperture or peristome of the shell may be simple or variously modified. An outer and an inner (columellar) lip are generally recognized. These may be continuous with each other, or may be divided below by an anterior notch. This, in some types (Fusinus, etc.) it is drawn out into an anterior siphonal canal, of greater or lesser length.

An upper or posterior notch is present in certain taxa, and this may result in the formation of a ridge or shelf next to the suture (Clavilithes). An outer (lateral) emargination or notch, sometimes prolonged into a slit occurs in certain types (Pleurotomidae, Pleurotomaridae, Bellerophontidae, etc.), and the progressive closing of this slit may give rise to a definitely marked slit band. In some cases the slit is abandoned and left as a hole (Fissurellidae), or by periodic renewal as a succession of holes (Haliotis). The outer emargination is often only indicated by the reflected course of the lines of growth on the shell.

On the inside of the outer lip, various ridges or plications called lirae are sometimes found, and these occasionally may be strong and tooth-like (Nerinea). Similar ridges or columellar plicae or folds are more often found on the inner lip, next to the columella or central spiral twist. These may be oblique or normal to the axis of coiling (horizontal), few or numerous, readily seen, or far within the shell so as to be invisible except in broken shells. When the axis of coiling is hollow (perforate spire) the opening at the base constitutes the umbilicus. The umbilicus varies greatly in size, and may be wholly or in part covered by an expansion or callus of the inner lip (Natica).

Many Recent shells, when the animal is alive or the shell is freshly empty, have an uppermost shell layer of horny, smooth, or hairy epidermis or periostracum, a proteinaceous layer which sometimes is thick enough to hide the color markings of the surface of the shell. The periostracum, as well as the coloration, is only rarely preserved in fossil shells.

The apertural end of the gastropod shell is the anterior end, nearest to the head of the animal; the apex of the spire is often the posterior end or at least is the dorsal side. Most authors figure the shells with the apex of the spire uppermost. In life, when the soft parts of these snail are retracted, in some groups the aperture of the shell is closed by using a horny or calcareous operculum, a door-like structure which is secreted by, and attached to, the upper surface of the posterior part of the foot. The operculum is of very variable form in the different groups of snails that possess one.[7]

Parts of the shell

A drawing of an abnormal scalarid form of the shell of the garden snail, Helix aspersa

The terminology used to describe the shells of gastropods includes:

Shape of the shell

The distinction of the shape of the shell may vary, based on the purpose. For example, distinguishing into three groups can be based on the height – width ratio:[8]

The following are the principal modifications of form in the gastropod shell.[9]

Detailed distinction of the shape can be:[10][11]

Pear shape means both shapes: ovate-conic and conic.

Schematic representation of the apical, apertural and basal view of a shell, showing 14 different commonly used measurements. Dotted lines represent the orientation axes (except of lower image).


The most frequently used measurements of a gastropod shell are: the height of the shell, the width of the shell, the height of the aperture and the width of the aperture. The number of whorls is also often used.

In this context, the height (or the length) of a shell is its maximum measurement along the central axis. The width (or breadth, or diameter) is the maximum measurement of the shell at right angles to the central axis. Both terms are only related to the description of the shell and not to the orientation of the shell on the living animal.

The largest height of any shell is found in the marine snail species Syrinx aruanus, which can be up to 91 cm.[12]

The central axis is an imaginary axis along the length of a shell, around which, in a coiled shell, the whorls spiral. The central axis passes through the columella, the central pillar of the shell.

Evolutionary changes

Among proposed roles invoked the variability of shells during evolution include mechanical stability,[13] defense against predators[14] (evolution of shells against external attacks has been proved by nanoindentation),[15] sexual selection[16] and climatic selection.[17][18]

The shell of some gastropods have been reduced or partly reduced during the evolution. This reduction can be seen in all slugs, in semi-slugs and in various other marine and non-marine gastropods. Sometimes the reduction of the shell is associated with predatory way of feeding.

Some taxa even lost the coiling of their shell during evolution.[19] According to Dollo's law, it is not possible to regain the coiling of the shell after it is lost. Despite that, there are few genera in the family Calyptraeidae that changed their developmental timing (heterochrony) and gained back (re-evolution) a coiled shell from the previous condition of an uncoiled limpet-like shell.[19]

Taphonomic implications

In large enough quantities, gastropod shells can have enough of an impact on environmental conditions to affect the ability of organic remains in the local environment to fossilize.[20] For example, in the Dinosaur Park Formation, fossil hadrosaur eggshell is rare.[20] This is because the breakdown of tannins from local coniferous vegetation would have caused the ancient waters to become acidic.[20] Eggshell fragments are present in only two microfossil sites, both of which are predominated by the preserved shells of invertebrate life, including gastropods.[20] It was the slow dissolution of these shells releasing calcium carbonate into the water that raised the water's pH high enough to prevent the eggshell fragments from dissolving before they could be fossilized.[20]

Variety of forms


This article incorporates public domain text from references,[1][6][7] and CC-BY-2.0 text from reference.[18]

  1. 1 2 John. B. Burch (1962). "How to Know the eastern land snails; pictured-key for determining the land snails of the United States occurring east of the Rocky Mountain Divide" WM. C. Brown Company Publishers, Dubuque, Iowa. 214 pages.
  2. Schilthuizen M. & Davison A. (2005). "The convoluted evolution of snail chirality". Naturwissenschaften 92(11): 504–515. {{DOI|10.1007/s00114-005-0045-2}}.
  3. "Amphidromus perversus (Linnaeus, 1758)".
  4. Myers P. Z. (13 April 2009) "Snails have nodal!". The Panda's Thumb, accessed 3 May 2009.
  5. Keisuke Shimizu, Minoru Iijima, Davin HE SetiamargaIsao Sarashina, Tetsuhiro Kudoh, Takahiro Asami, Edi Gittenberger, Kazuyoshi Endo; Left-right asymmetric expression of dpp in the mantle of gastropods correlates with asymmetric shell coiling, EvoDevo 2013, 4:15
  6. 1 2 3 4 5 6 7 8 9 10 11 12 13 Laidlaw F. F. & Solem A. (1961). "The land snail genus Amphidromus: a synoptic catalogue". Fieldiana Zoology 41(4): 505-720.
  7. 1 2 Grabau A. W. & Shimer H. W. (1909) North American Index Fossils Invertebrates. Volume I.. A. G. Seiler & Company, New York. pages page 582-584.
  8. Falkner G., Obrdlík P., Castella E. & Speight M. C. D. (2001). Shelled Gastropoda of Western Europe. München: Friedrich-Held-Gesellschaft, 267 pp.
  9. George Washington Tryon, Structural and systematic conchology, 1882, p. 43-44
  10. Hershler R. & Ponder W. F.(1998). "A Review of Morphological Characters of Hydrobioid Snails". Smithsonian Contributions to Zoology 600: 1-55. .
  11. Dance P. S. (). Shells.
  12. Wells F. E., Walker D. I. & Jones D. S. (eds.) (2003) "Food of giants – field observations on the diet of Syrinx aruanus (Linnaeus, 1758) (Turbinellidae) the largest living gastropod". The Marine Flora and Fauna of Dampier, Western Australia. Western Australian Museum, Perth.
  13. Britton J. C (1995) "The relationship between position on shore and shell ornamentation in 2 size-dependent morphotypes of Littorina striata, with an estimate of evaporative water-loss in these morphotypes and in Melarhaphe neritoides". Hydrobiologia 309: 129-142. abstract.
  14. Wilson A. B., Glaubrecht M. & Meyer A. (March 2004) "Ancient lakes as evolutionary reservoirs: evidence from the thalassoid gastropods of Lake Tanganyika". Proceedings of Royal Society London Series B – Biological Sciences 271: 529-536. doi:10.1098/rspb.2003.2624.
  15. Bignardi C., Petraroli M. & Pugno N. M. (2010). "Nanoindentations on Conch Shells of Gastropoda and Bivalvia Molluscs Reveal Anisotropic Evolution Against External Attacks". Journal of Nanoscience and Nanotechnology 10(10): 6453-6460. doi:10.1166/jnn.2010.2626.
  16. Schilthuizen M. (5 June 2003) "Sexual selection on land snail shell ornamentation: a hypothesis that may explain shell diversity". BMC Evolutionary Biology 3: 13. doi:10.1186/1471-2148-3-13.
  17. Goodfriend G. A. (1986) "Variation in land-snail shell form and size and its causes – a Review". Systematic Zoology 35: 204-223.
  18. 1 2 Pfenninger M., Hrabáková M., Steinke D. & Dèpraz A. (4 November 2005) "Why do snails have hairs? A Bayesian inference of character evolution". BMC Evolutionary Biology 5: 59. doi:10.1186/1471-2148-5-59
  19. 1 2 Collin R. & Cipriani R. (22 December 2003) "Dollo’s law and the re-evolution of shell coiling". Proceedings of the Royal Society B 270(1533): 2551–2555. doi:10.1098/rspb.2003.2517 PMID 14728776.
  20. 1 2 3 4 5 Tanke, D.H. and Brett-Surman, M.K. 2001. Evidence of Hatchling and Nestling-Size Hadrosaurs (Reptilia:Ornithischia) from Dinosaur Provincial Park (Dinosaur Park Formation: Campanian), Alberta, Canada. pp. 206-218. In: Mesozoic Vertebrate Life—New Research Inspired by the Paleontology of Philip J. Currie. Edited by D.H. Tanke and K. Carpenter. Indiana University Press: Bloomington. xviii + 577 pp.

Further reading

about chirality

External links

This article is issued from Wikipedia - version of the 12/2/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.