Ostreoidea | |
---|---|
Pacific oyster, Magallana gigas | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Mollusca |
Class: | Bivalvia |
Subclass: | Pteriomorphia |
Order: | Ostreida |
Superfamily: | Ostreoidea Rafinesque, 1815 |
Families | |
Ostreoidea is a taxonomic superfamily of bivalve marine mollusc, sometimes simply identified as oysters, [1] containing two families. The ostreoids are characterized in part by the presence of a well developed axial rod. [2] Anal flaps are known to exist within the family Ostreidae but not within the more-primitive Gryphaeidae. [3] The scar from the adductor muscle is simple, with a single, central scar. [4] In the majority, the right valve is less convex than the left. [5]
Harold Harry (1985) gives a detailed description of the morphological and anatomical features that are common in the superfamily. [6] In this section, oyster is used to mean "members of Ostreoidea".
Oysters of this group generally attach to a substrate by cementing their left valve to it. The two valves are unequal: the attached left valve is larger and more cupped than the right 'lid' (to a greater or lesser extent, depending on the species).
The lips of the mantle lobes are joined at the edge opposite the hinge (ventral or posteroventral edge, the hinge is conventionally designated as the dorsal direction). This forms two chambers, one on either side of the visceral mass. The ingress chamber is anatomically anterior and the egress chamber is posterior. [6] : 123–124 Within Ostreoidea, the degree of attachment of the left and right mantle lobes to the visceral mass varies between subgroups. The may be one (right) or two passages (left and right), or none, around the body between the adductor and hinge (termed either supramyal or promial passages). [6] : 125
Oysters are monomyarian, having one adductor muscle. This is the posterior of the ancestral pair; the anterior muscle is not present in post-larval stages. The adductor is divided into visible halves of translucent "quick" muscle tissue and opaque "catch" tissue. Oysters also lack a foot and the associated body muscles: the foot disappears in early larval stages. This is in contrast to other bivalves with reduced or missing feet where the process occurs later in development. [6] : 123
Bivalvia or bivalves, in previous centuries referred to as the Lamellibranchiata and Pelecypoda, is a class of aquatic molluscs that have laterally compressed soft bodies enclosed by a calcified exoskeleton consisting of a hinged pair of half-shells known as valves. As a group, bivalves have no head and lack some typical molluscan organs such as the radula and the odontophore. Their gills have evolved into ctenidia, specialised organs for feeding and breathing.
Scallop is a common name that encompasses various species of marine bivalve mollusks in the taxonomic family Pectinidae, the scallops. However, the common name "scallop" is also sometimes applied to species in other closely related families within the superfamily Pectinoidea, which also includes the thorny oysters.
The Ostreidae, the true oysters, include most species of molluscs commonly consumed as oysters. Pearl oysters are not true oysters, and belong to the order Pteriida.
The order Ostreida includes the true oysters. One superfamily (Ostreoidea) and two extant families are recognised within it. The two families are Ostreidae, the true oysters, and Gryphaeidae, the foam oysters.
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 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.
Freshwater bivalves are molluscs of the order Bivalvia that inhabit freshwater ecosystems. They are one of the two main groups of freshwater molluscs, along with freshwater snails.
A bivalve shell is the enveloping exoskeleton or shell of a bivalve mollusc, composed of two hinged halves or valves. The two half-shells, called the "right valve" and "left valve", are joined by a ligament and 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.
Anodontia alba, or the buttercup lucine, is a species of bivalve mollusc in the family Lucinidae. It can be found along the Atlantic coast of North America, its range extending from North Carolina in the United States to the West Indies.
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.
Venerupis decussata is a marine bivalve mollusc in the family Veneridae, commonly known as the cross-cut carpet shell.
Thracia convexa is a bivalve mollusc in the family Thraciidae.
Donax vittatus, or the banded wedge shell, is a species of bivalve mollusc in the order Cardiida. It is found on beaches in northwest Europe buried in the sand on the lower shore.
Protobranchia is a subclass of bivalve molluscs. It contains the extant orders Nuculanida, Nuculida, and Solemyida.
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.
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 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 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.
The pallial line is a mark on the interior of each valve of the shell of a bivalve mollusk. This line shows where all of the mantle muscles were attached in life. In clams with two adductor muscles the pallial line usually joins the marks known as adductor muscle scars, which are where the adductor muscles attach.
The adductor muscles are the main muscular system in bivalve mollusks. In many parts of the world, when people eat scallops, the adductor muscles are the only part of the animal which is eaten. Adductor muscles leave noticeable scars or marks on the interior of the shell's valves. Those marks are often used by scientists who are in the process of identifying empty shells to determine their correct taxonomic placement.
Ostrea equestris, commonly known as the crested oyster or horse oyster, is a species of bivalve mollusc in the family Ostreidae. It can be found along the Atlantic coast of North and South America, ranging from Virginia to Patagonia.