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. The shipworms bore into wood, clay, or stone and live inside these substances.
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.
The Gryphaeidae, common name the foam oysters or honeycomb oysters, are a family of marine bivalve mollusks. This family of bivalves is very well represented in the fossil record, however the number of living species is very few.
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.
Exogyra is an extinct genus of fossil marine oysters in the family Gryphaeidae, the foam oysters or honeycomb oysters. These bivalves grew cemented by the more cupped left valve. The right valve is flatter, and the beak is curved to one side. Exogyra lived on solid substrates in warm seas during the Jurassic and Cretaceous periods.
Juliidae, common name the bivalved gastropods, is a family of minute sea snails, marine gastropod mollusks or micromollusks in the superfamily Oxynooidea, an opisthobranch group.
Pojetaia is an extinct genus of early bivalves, one of two genera in the extinct family Fordillidae. The genus is known solely from Early to Middle Cambrian fossils found in North America, Greenland, Europe, North Africa, Asia, and Australia. The genus currently contains two accepted species, Pojetaia runnegari, the type species, and Pojetaia sarhroensis, though up to seven species have been proposed. The genera Buluniella, Jellia, and Oryzoconcha are all considered synonyms of Pojetaia.
Tellimya ferruginosa is a species of small marine bivalve mollusc in the family Lasaeidae. It is found on the eastern side of the Atlantic Ocean.
Lutraria is a genus of medium-sized marine bivalve mollusks or clams, commonly known as otter shells.
Cassianellidae is a small extinct family of prehistoric bivalves which lived from the Middle Triassic, Ladinian stage through the Late Triassic Norian stage. It has been suggested that the family may have evolved from the related family Bakevelliidae. Bakevelliidae species are found in North America, South America, Europe, the Middle East, and Asia. Living a stationary life attached to substrate in marine and brackish environments, they formed shells of an aragonite composition with a low amount of magnesium calcite. The family Cassianellidae was named by K. Ichikawa in 1958.
Fordillidae is an extinct family of early bivalves and one of two families in the extinct superfamily Fordilloidea. The family is known from fossils of early to middle Cambrian age found in North America, Greenland, Europe, the Middle East, Asia, and Australia. The family currently contains two genera, Fordilla and Pojetaia, each with up to three described species. Due to the size and age of the fossil specimens, Fordillidae species are included as part of the Turkish Small shelly fauna.
Fordilloidea is an extinct superfamily of early bivalves containing two described families, Fordillidae and Camyidae and the only superfamily in the order Fordillida. The superfamily is known from fossils of early to middle Cambrian age found in North America, Greenland, Europe, the Middle East, Asia, and Australia. Fordillidae currently contains two genera, Fordilla and Pojetaia each with up to three described species while Camyidae only contains a single genus Camya with one described species, Camya asy. Due to the size and age of the fossil specimens, Fordillidae species are included as part of the Turkish Small shelly fauna.
Emiliodonta is an extinct genus of bivalve in the extinct family Praenuculidae. The genus is one of three genera in the subfamily Concavodontinae. Emiliodonta is known solely from late Ordovician, Caradocian epoch, fossils found in South America. The genus contains a single accepted species, Emiliodonta cuerdai.
Villicumia is an extinct genus of bivalve in the extinct family Praenuculidae. The genus is one of eleven genera in the subfamily Praenuculinae. It is one of three Praenuculinae genera known solely from late Ordovician, Caradoc epoch, fossils found in South America. Villicumia currently contains a single accepted species, Villicumia canteraensis.
Trigonoconcha is an extinct genus of bivalve in the extinct family Praenuculidae. The genus is one of eleven genera in the subfamily Praenuculinae. It is one of three Praenuculinae genera known solely from Late Ordivician, Caradoc epoch, fossils found in South America. Trigonoconcha currently contains a single accepted species, Trigonoconcha acuta.
Panenka is a genus of fossil saltwater clams, marine bivalve molluscs in the family Praecardiidae. Like most bivalves, these molluscs were suspension feeders. They lived in the Devonian Period.
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. Like the ligament, the hinge teeth are also situated along the hinge line of the shell, in most cases.
A resilifer is a part of the shell of certain bivalve mollusks. It is either a recess or a process, the function of which is the attachment of an internal ligament, which holds the two valves together.
A hinge ligament is a crucial part of the anatomical structure of a bivalve shell, i.e. the shell of a bivalve mollusk. The shell of a bivalve has two valves and these are joined together by the ligament at the dorsal edge of the shell. The ligament is made of a strong, flexible and elastic, fibrous, proteinaceous material which is usually pale brown, dark brown or black in color.
Gervillia is an extinct genus of prehistoric bivalves belonging to the family Bakevelliidae.
