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Home -> Kingdom Animalia -> Phylum Mollusca -> Class Scaphopoda

Class Scaphopoda
tusk shells



2009/11/15 05:03:22.648 US/Eastern

By Renee Sherman Mulcrone

Kingdom: Animalia
Phylum: Mollusca
Class: Scaphopoda
Members of this Class

Diversity

There are approximately 900 species of Scaphopoda, commonly called tusk shells. (Brusca and Brusca, 2003)

Geographic Range

Scaphopods are found in marine regions around the world. (Brusca and Brusca, 2003; Jones and Baxter, 1987)

Biogeographic Regions:
indian ocean; atlantic ocean ; pacific ocean ; mediterranean sea.

Habitat

Scaphopods are all marine species whose habitat ranges from shallow sub-littoral areas up to waters that are 4570 m deep. Most scaphopods are found in waters greater than 6 m. Scaphopods burrow in sediments ranging from muds to medium-coarse gravel. The two orders of this group may have slightly differing burrowing behaviors. Individuals in the Gadilida may burrow up to 30 cm in captivity. Many species in the Dentaliida burrow with the concave side just below the substrate. (Barnes, 1987; Jones and Baxter, 1987; Lamprell and Healy, 2001; Spear, 1994)

These animals are found in the following types of habitat:
saltwater or marine .

Aquatic Biomes:
benthic ; coastal .

Systematic and Taxonomic History

Scaphopods have a fossil record dating back to the early Devonian. Scaphopoda means "shovel foot". Scaphopods are most closely related to bivalves and share four synapomorphies: 1) reduced head, 2) decentralized nervous system, 3) mantle cavity is expanded to surround the body and 4) foot modified into a spate form.

Within the Scaphopoda, two subtaxa are recognized, the orders Dentaliida (Gray, 1847) and Gadilida (Stoliczka, 1862). The Gadilida has a constriction on the anterior aperature and the central tooth of the radula is square or higher than wide. The Dentaliida have a conical foot, the shells are often ribbed, they may be small to large and the central tooth of the radula is wider than high. While the distinction of the orders has been clear, the taxonomy of genera among families has been debated. (Brusca and Brusca, 2003; Jones and Baxter, 1987; Lamprell and Healy, 2001; Reynolds, 1996; Spear, 1994)

Synapomorphies
  • tusk shaped, open ended shell
  • ctenidia lost
  • captacula (threadlike tentacles)

Physical Description

Scaphopod shells usually have four layers, and these are used for identification. The shell is curved, tubular, and shaped like an elephant tusk. Most average 3 to 6 cm long, but can range from 4 mm to 15 cm. Fossils show specimens 30 cm long.

The scaphopod shell is open at both ends. The wider end of the shell where the head and foot extends out is the anterior end. The posterior is the narrow end of the shell which usually is at or below the substrate.

The shell surrounds a large mantle cavity, and wraps around the viscera to form a tube. The mantle cavity goes along ventral side to a smaller opening at the other end. No ctenidia are present, and gas exchange is through the mantle surface. Cilia an currents move water thorugh posterior aperature. Occasional muscular contractions expell water from the posterior end of the shell.

The head is a short, conical projection (probosicis) with a mouth. Lobes on each side of the head have threadlike tentacles, called captacula, which are used to capture food. (Barnes, 1987; Reynolds, 1996; Shimek, 2005)

Some key physical features:
heterothermic ; homoiothermic; bilateral symmetry .

Development

After fertilization, the egg develops into a free-swimming trocophore larvae, then a bilaterally symmetrical veliger. The veliger usually metamorphoses in 5-6 days. At this point it becomes benthic. (Barnes, 1987; Jones and Baxter, 1987)

Special features of growth:
metamorphosis .

Reproduction

Scaphopods are gonochoristic or dioecious. Eggs are released singly through the right nephridium. Sperm is also released through the nephridium. Eggs are planktonic and fertilization is external. (Barnes, 1987)

Key reproductive features:
gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization (external ); oviparous .

There is no parental investment after release of gametes. (Brusca and Brusca, 2003)

Parental investment:
pre-fertilization (provisioning).

Behavior

Scaphopods burrow by projecting their foot into the substrate and contracting pedal retractor muscles to pull the animal downward. Extension of the foot may help with water intake, and the scaphopods probably use foot movements to expel wastes from the posterior opening.

The two orders of this group may have slightly differing burrowing behaviors. Individuals in the Gadilida burrow up to 30 cm in captivity and burrow this deep in the ocean. Many species in the Dentaliida burrow with the concave side just below the substrate. (Brusca and Brusca, 2003; Jones and Baxter, 1987; Lamprell and Healy, 2001; Shimek, 2005)

Key behaviors:
motile ; sedentary .

Communication and Perception

The scapopod captacula may have tactile receptors, but this is unknown. Scaphopods have lost eyes, tentacles and osphridia found in other molluscs. The buccal cavity has a sub-radular (below the radula) organ which may be chemoreceptive. (Brusca and Brusca, 2003; Jones and Baxter, 1987)

Perception channels:
tactile ; chemical .

Food Habits

Scaphopods are selective deposit feeders, mainly feeding on microscopic organisms, particularly diatoms and foraminiferans. Each tentacle of the capatula has an adhesive know at the tip to capture prey. Tentacular cilia brings smaller particles back to the scaphopod mouth. The tentacles retract to bring larger items to the mouth. The radula is used to break down prey. Food is digested extracellularly in the stomach, then travels from the stomach to intestine. Waste is expelled into mantle cavity through the anus. (Barnes, 1987)

Primary Diet:
omnivore .

Predation

Known predators
  • fish
  • crabs

Scaphopods are fed on by fish and crabs. Their burrowing behavior is thought to keep them from predators. (Shimek, 2005)

Ecosystem Roles

Scaphopods selectively feed on sediments, although the importance of this in the ecosystem is unknown. Hermit crabs are known to use the shells. (Shimek, 2005)

Economic Importance for Humans: Positive

Shells of the genus Dentalium were culturally significant with Pacific Northwest natives (Amerinds)until the late 1800s. The shells were collected on strings and used as necklaces and money. (Reynolds, 1996; Spear, 1994)

Ways that people benefit from these animals:
body parts are source of valuable material.

Conservation

No scaphopods are currently listed or given special status.

Contributors

Renee Sherman Mulcrone (author).

References

Barnes, R. 1987. Invertebrate Zoology. Orlando, Florida: Dryden Press.

Brusca, R., G. Brusca. 2003. Invertebrates. Sunderland, Massachusetts: Sinauer Associates, Inc..

Jones, A., J. Baxter. 1987. Molluscs: Caudofoveata, Solenogastres, Polyplacophora and Scaphopoda. London: E. J. Brill/Dr. W. Backhuys.

Lamprell, K., J. Healy. 2001. Scaphopoda. Pp. 85-128 in A. Wells, W. W. K. Houston, eds. Zoological Catalogue of Australia, Vol. 17.2. Melbourne, Australia: CSIRO Publishing.

Reynolds, P. 1996. "The Scaphopod Page, Class Scaphopoda, Phylum Mollusca" (On-line). Accessed February 04, 2005 at http://academics.hamilton.edu/biology/preynold/Scaphopoda/default.html.

Shimek, R. 1990. Diet and habitat utilization in a Northeastern Pacific Ocean scaphopod assemblage. American Malacological Bulletin, 7: 147-169.

Shimek, R. 2005. "Scaphopods, Some Natural History" (On-line). Accessed February 04, 2005 at http://rshimek.com/Scaph1.htm.

Spear, B. 1994. "Introduction to the Scaphopoda, the tusk shells" (On-line). Accessed February 04, 2005 at http://www.ucmp.berkeley.edu/mollusca/scaphs/scaphopoda.html.

2009/11/15 05:03:24.377 US/Eastern

To cite this page: Mulcrone, R. 2005. "Scaphopoda" (On-line), Animal Diversity Web. Accessed November 22, 2009 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Scaphopoda.html.

Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.

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