Hinge teeth are part of the anatomical structure of the inner surface of a bivalve shell, i.e. the shell of a bivalve mollusk. Bivalves by definition have two valves, which are joined together by a strong and flexible ligament situated on the hinge line at the dorsal edge of the shell. In life, the shell needs to be able to open slightly to allow the foot and siphons to protrude, and then close again, without the valves moving out of alignment with one another. To make this possible, in most cases the two valves are articulated using an arrangement of structures known as hinge teeth (often referred to collectively as the "dentition"). Like the ligament, the hinge teeth are also situated along the hinge line of the shell, in most cases.
In most families of bivalves, the two valves of the shell are almost perfectly symmetrical with one another along the hinge line, although the placement and shape of the teeth may differ slightly in the left valve and right valve in order for the two valves to articulate properly.
Each related group of bivalves tends to have distinctive hinge teeth, and because of this, examining the arrangement of the hinge teeth in a bivalve shell is often essential for identification and classification.
A formal terminology is used to describe the different types of dentition.
The hinge teeth, or the lack thereof, is an important feature in identifying bivalves because the teeth are generally similar within the major taxonomic groups. Historically the hinge teeth have provided a convenient means by which to construct classification schemes and attempt to indicate the phylogenetic relationships within the class Bivalvia. [1] [2] [3] [4] There are formal names for the various types of hinge tooth arrangements or dentition.
The taxodont hinge shows either one or two rows of similar interlocking teeth on either side of the umbones, as is the case in the ark clams (Arcidae), the bittersweets (Glycymerididae), and the nut clams (Nuculidae).
The dysodont hinge shows a strong ligament along the hinge line, with weak teeth near the umbones, as in the marine mussels (Mytilidae).
The isodont hinge has lateral tubercles and sockets on either side of a thick ligament which is referred to as a resilium. This arrangement is typical of the oysters (Ostreidae), scallops (Pectinidae), thorny oysters (Spondylidae), and kittens paws (Plicatulidae).
The crurae hinge has lamellar ridges on or near the hinge plate, and these function as hinge teeth. This arrangement is characteristic of the Pandoridae, the jingle shells Anomiidae, and Dimyidae.
The schizodont hinge has reverse V-shaped scissurate teeth, and often an elongated lateral tooth. This arrangement is found in most Unionidae freshwater mussels.
The pachyodont hinge has large obscure tubercules with corresponding pits on the opposite valve. This arrangement is characteristic of the Chamidae, the jewel boxes.
The heterodont hinge has two to three wedge-shaped cardinal teeth set in the center near the umbones, and generally also has elongated lateral teeth on the anterior and posterior margins (on one or both sides). This arrangement is characteristic of the venus clams (Veneridae), the cockles (Cardiidae) and several other important groups.
In the desmodont hinge, also known as an asthenodont hinge, the hinge consists of a large ligamentous resilifer (or chondrophore) which replaces the cardinal teeth, as in the soft-shell clams (Myidae).
The anodont hinge is characterized by a strong ligament (or a series of transverse ligamental grooves as in the Isognomonidae), however, true teeth are absent in adults as is the case in the pen shells (Pinnidae), tree oysters (Isognomonidae), the pearl oysters (Pteriidae), and some freshwater mussels such as the genus Anodonta .
Bivalvia, in previous centuries referred to as the Lamellibranchiata and Pelecypoda, is a class of marine and freshwater molluscs that have laterally compressed bodies enclosed by a shell consisting of two hinged parts. As a group, bivalves have no head and they lack some usual molluscan organs, like the radula and the odontophore. The class includes the clams, oysters, cockles, mussels, scallops, and numerous other families that live in saltwater, as well as a number of families that live in freshwater. The majority are filter feeders. The gills have evolved into ctenidia, specialised organs for feeding and breathing. Most bivalves bury themselves in sediment, where they are relatively safe from predation. Others lie on the sea floor or attach themselves to rocks or other hard surfaces. Some bivalves, such as the scallops and file shells, can swim. Shipworms bore into wood, clay, or stone and live inside these substances.
A cockle is an edible marine bivalve mollusc. Although many small edible bivalves are loosely called cockles, true cockles are species in the family Cardiidae.
The Arcida is an extant order of bivalve molluscs. This order dates back to the lower Ordovician period. They are distinguished from related groups, such as the mussels, by having a straight hinge to the shells, and the adductor muscles being of equal size. The duplivincular ligament, taxodont dentition, and a shell microstructure consisting of the outer crossed lamellar and inner complex crossed lamellar layers are defining characters of this order.
The Veneridae or venerids, common name: Venus clams, are a very large family of minute to large, saltwater clams, marine bivalve molluscs. Over 500 living species of venerid bivalves are known, most of which are edible, and many of which are exploited as food sources.
Ark clam is the common name for a family of small to large-sized saltwater clams or marine bivalve molluscs in the family Arcidae. Generally less than 80 mm long, ark clams vary both in shape and size. They number about 200 species worldwide.
The Pteriomorphia comprise a subclass of saltwater clams, marine bivalve molluscs. It contains several major orders, including the Arcida, Ostreida, Pectinida, Limida, Mytilida, and Pteriida. It also contains some extinct and probably basal families, such as the Evyanidae, Colpomyidae, Bakevelliidae, Cassianellidae, and Lithiotidae.
Chione cancellata, is a species of medium-sized saltwater clam, a marine bivalve mollusc in the family Veneridae, the venus clams.
Freshwater bivalves are one kind of freshwater mollusc, along with freshwater snails. They are bivalves that live in fresh water as opposed to salt water, which is the main habitat type for bivalves.
A valve is each articulating part of the shell of a mollusc or another multi-shelled animal such as brachiopods and some crustaceans. Each part is known as a valve or in the case of chitons, a "plate". Members of two classes of molluscs, the Bivalvia (clams) and the Polyplacophora (chitons), have valves.
A bivalve shell is part of the body, the exoskeleton or shell, of a bivalve mollusk. In life, the shell of this class of mollusks is composed of two hinged parts or valves. Bivalves are very common in essentially all aquatic locales, including saltwater, brackish water, and freshwater. The shells of bivalves commonly wash up on beaches and along the edges of lakes, rivers, and streams. Bivalves by definition possess two shells or valves, a "right valve" and a "left valve", that are joined by a ligament. The two valves usually articulate with one another using structures known as "teeth" which are situated along the hinge line. In many bivalve shells, the two valves are symmetrical along the hinge line—when truly symmetrical, such an animal is said to be equivalved; if the valves vary from each other in size or shape, inequivalved. If symmetrical front-to-back, the valves are said to be equilateral, and are otherwise considered inequilateral.
Leukoma staminea, commonly known as the Pacific littleneck clam, the littleneck clam, the rock cockle, the hardshell clam, the Tomales Bay cockle, the rock clam or the ribbed carpet shell, is a species of bivalve mollusc in the family Veneridae. This species of mollusc was exploited by early humans in North America; for example, the Chumash peoples of Central California harvested these clams in Morro Bay approximately 1,000 years ago, and the distinctive shells form middens near their settlements.
The grooved carpet shell, or Palourde clam, Ruditapes decussatus, or Venerupis decussatus, is a clam in the family Veneridae. It is distributed worldwide and is highly prized due to its ecological and economic interest. It has been proposed as a bioindicator.
The Pectinoidea are a superfamily of marine bivalve molluscs, including the scallops and spiny oysters.
Pectinida is a taxonomic order of large and medium-sized saltwater clams, marine bivalve molluscs, commonly known as scallops and their allies. It is believed that they began evolutionarily in the late Middle Ordovician epoch; many species, of course, are still extant.
Venerupis corrugata, the pullet carpet shell, is a species of bivalve mollusc in the family Veneridae. It is found buried in the sediment on the sea bed in shallow parts of the eastern Atlantic Ocean. It is harvested for human consumption in Spain and other parts of Western Europe.
Arcuatula perfragilis is a bivalve mollusc of the mussel family, Mytilidae, which has an Indo-Pacific distribution including the Red Sea. It has invaded the eastern Mediterranean from the Red Sea by way of the Suez Canal, a process known as Lessepsian migration.
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