Phylactolaemata | |
---|---|
Zooid of a Phylactoaemata colony | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Bryozoa |
Class: | Phylactolaemata |
Order: | Plumatellida |
Families | |
Phylactolaemata [1] is a class of the phylum Bryozoa whose members live only in freshwater environments. Like all bryozoans, they filter feed by means of an extensible "crown" of ciliated tentacles called a lophophore, and like nearly all bryozoans (the only known exception being Monobryozoon ), they live in colonies, each of which consists of clones of the founding member. Unlike those of some marine bryozoans, phylactolaemate colonies consist of only one type of zooid, the feeding forms known as autozooids. [2] These are supported by an unmineralized "exoskeleton" made of gelatinous material or protein, secreted by the zooids. [3] The class contains only one extant order, Plumatellida. [4]
Phylactolaemata is regarded to have been the earliest group of bryozoans to evolve. However, because they did not have calcified skeletons, these early bryozoans would have had very low potential to fossilize. Fossils of phylactolaemate statoblasts, which consist of protective chitinous shells that serve as protection for dormant masses of cells holding the potential to grow new colonies, have been found rarely, dating back to the Permian. It is possible that the absence of statoblasts in earlier rocks is because statoblasts evolved as an adaptation for surviving in freshwater, and earlier phylactolaemates were marine. [5]
Phylactolaemate colonies reproduce sexually, and each member is a simultaneous hermaphrodite that functions as both male and female. [2] They also reproduce asexually by a method that is unique among bryozoans and enables a colony's lineage to survive the variable and uncertain conditions of freshwater environments. [3] Among the classes of the bryozoans, the phylactoaemata have the most aberrant spermatozoon. [6] Throughout summer and autumn they produce disc-shaped statoblasts, masses of cells that function as "survival pods" rather like the gemmules of sponges. [2] Statoblasts form on the funiculus (cord) connected to the parent's gut, which nourishes them. [3] As they grow, statoblasts develop protective bivalve-like shells made of chitin. When they mature, some types stick to the parent colony, some fall to the bottom, some contain air spaces that enable them to float, [2] and some remain in the parent's cystid (outer casing) to re-build the colony if it dies. [3] Statoblasts can remain dormant for considerable periods, and while dormant can survive harsh conditions such as freezing and desiccation. They can be transported across long distances by animals, floating vegetation, currents [2] and winds. [3] When conditions improve, the valves of the shell separate and the cells inside develop into a zooid that tries to form a new colony. A study estimated that one group of colonies in a patch 1 square meter (11 sq ft) produced 800,000 statoblasts. [2]
Bryozoa are a phylum of simple, aquatic invertebrate animals, nearly all living in sedentary colonies. Typically about 0.5 millimetres long, they have a special feeding structure called a lophophore, a "crown" of tentacles used for filter feeding. Most marine bryozoans live in tropical waters, but a few are found in oceanic trenches and polar waters. The bryozoans are classified as the marine bryozoans (Stenolaemata), freshwater bryozoans (Phylactolaemata), and mostly-marine bryozoans (Gymnolaemata), a few members of which prefer brackish water. 5,869 living species are known. At least two genera are solitary ; the rest are colonial.
In biology, a colony is composed of two or more conspecific individuals living in close association with, or connected to, one another. This association is usually for mutual benefit such as stronger defense or the ability to attack bigger prey.
Entoprocta, or Kamptozoa, is a phylum of mostly sessile aquatic animals, ranging from 0.1 to 7 millimetres long. Mature individuals are goblet-shaped, on relatively long stalks. They have a "crown" of solid tentacles whose cilia generate water currents that draw food particles towards the mouth, and both the mouth and anus lie inside the "crown". The superficially similar Bryozoa (Ectoprocta) have the anus outside a "crown" of hollow tentacles. Most families of entoprocts are colonial, and all but 2 of the 150 species are marine. A few solitary species can move slowly.
Stenolaemata are a class of exclusively marine bryozoans. Stenolaemates originated and diversified in the Ordovician, and more than 600 species are still alive today. All extant (living) species are in the order Cyclostomatida, the third-largest order of living bryozoans.
Cheilostomatida, also called Cheilostomata, is an order of Bryozoa in the class Gymnolaemata.
Membranipora membranacea is a very widely distributed species of marine bryozoan known from the Atlantic and Pacific Oceans, usually in temperate zone environments. This bryozoan is a colonial organism characterized by a thin, mat-like encrustation, white to gray in color. It may be known colloquially as the coffin box, sea-mat or lacy crust bryozoan and is often abundantly found encrusting seaweeds, particularly kelps.
Tetracapsuloides bryosalmonae is a myxozoan parasite of salmonid fish. It is the only species currently recognized in the monotypic genus Tetracapsuloides. It is the cause of proliferative kidney disease (PKD), one of the most serious parasitic diseases of salmonid populations in Europe and North America that can result in losses of up to 90% in infected populations.
Cyclostomatida, or cyclostomata, are an ancient order of stenolaemate bryozoans which first appeared in the Lower Ordovician. It consists of 7+ suborders, 59+ families, 373+ genera, and 666+ species. The cyclostome bryozoans were dominant in the Mesozoic; since that era, they have decreased. Currently, cyclostomes seldom constitute more than 20% of the species recorded in regional bryozoan faunas.
A zooid or zoöid is a single animal that is part of a colonial animal. This lifestyle has been adopted by animals from separate unrelated taxa. Zooids are multicellular; their structure is similar to that of other solitary animals. The zooids can either be directly connected by tissue or share a common exoskeleton. The colonial organism as a whole is called a zoon, plural zoa.
Celleporidae is a family of bryozoans – colonial, aquatic, invertebrates – in the order Cheilostomatida. Structurally, they are defined by densely packed zooids. The zooids usually have irregular direction, and are defined by morphological characteristics. Masses of the dead animals can form shallow sediments. Members of the family are recorded from every ocean, even around Antarctica, where they are represented primarily by the genus Osthimosia. Fossils of the family exist as old as from 235 million years ago, during the Triassic period.
Trepostomatida is an extinct order of bryozoans in the class Stenolaemata. Trepostome bryozoans possessed mineralized calcitic skeletons and are frequently fossilized; some of the largest known fossilized bryozoan colonies are branching trepostomes and massive dome-shaped trepostomes. Trepostomes did not have many specialized zooecia beyond ordinary feeding autozooecia. The two main known heteromorphs are exilazooecia and mesozooecia, which had the purpose of maintaining regular spacing between autozooecia.
Statoblasts are a means to reproduce asexually by a method that is unique among bryozoans and enables a colony's lineage to survive the variable and uncertain conditions of freshwater environments. Statoblasts are masses of cells that function as "survival pods" rather like the gemmules of sponges. Statoblasts form on the funiculus (cord) connected to the parent's gut, which nourishes them. As they grow, statoblasts develop protective bivalve-like shells made of chitin. When they mature, some types stick to the parent colony, some fall to the bottom, some contain air spaces that enable them to float, and some remain in the parent's cystid to re-build the colony if it dies. Statoblasts can remain dormant for considerable periods, and while dormant can survive harsh conditions such as freezing and desiccation. They can be transported across long distances by animals, floating vegetation, currents and winds. When conditions improve, the valves of the shell separate and the cells inside develop into a zooid that tries to form a new colony. A study estimated that one group of colonies in a patch 1 square meter (11 sq ft) produced 800,000 statoblasts.
Amathia vidovici is a species of colonial bryozoans with a tree-like structure. It is found in shallow waters over a wide geographical range, being found in both the Atlantic and Pacific Oceans and adjoining seas.
Fenestrata is an extinct order of bryozoan, dating from the Upper Arenig. Most fenestrate bryozoans formed net-like colonies, often in funnel- or fan-shaped forms, with a single layer of zooids facing one direction. The colony shape served as a filter-feeding apparatus that water currents flowed through, with autozooecial apertures only on the side of the colony facing into the current. This colony structure was vulnerable to predators, so some fenestrate bryozoans produced skeletal superstructures, likely to strengthen or protect the colony, and others had protective spines surrounding their autozooecial apertures.
Amathia verticillata, commonly known as the spaghetti bryozoan, is a species of colonial bryozoans with a bush-like structure. It is found in shallow temperate and warm waters in the western Atlantic Ocean and the Caribbean Sea and has spread worldwide as a fouling organism. It is regarded as an invasive species in some countries.
Fenestella is a genus of bryozoans or moss animals, forming fan–shaped colonies with a netted appearance. It is known from the Middle Ordovician to the early Upper Triassic (Carnian), reaching its largest diversity during the Carboniferous. Many hundreds of species have been described from marine sediments all over the world.
Electra pilosa is a species of colonial bryozoan in the order Cheilostomatida. It is native to the northeastern and northwestern Atlantic Ocean and is also present in Australia and New Zealand.
Bugula neritina is a cryptic species complex of sessile marine animal in the genus Bugula. It has a practically cosmopolitan distribution, being found in temperate and tropical waters around the world, and it has become an invasive species in numerous locations. It is often found in hard substrates, such as rocks, shells, pillars and ship hulls, where it can form dense mats, contributing to biofouling. B. neritina is of biomedical interest because it harbors a bacterial symbiont that produces a group of bioactive compounds with potential applications in the treatment of numerous diseases.
Chorizopora brongniartii is a species of bryozoan in the family Chorizoporidae. It is an encrusting bryozoan, the colonies forming spreading patches. It has a widespread distribution in tropical and temperate seas.
Lichenalia is an extinct genus of cystoporate bryozoan belonging to the family Rhinoporidae. It is known from the Upper Ordovician to the Middle Silurian periods, which spanned from approximately 460 to 430 million years ago. The genus had a cosmopolitan distribution, with fossil specimens found in various regions of the world, including North America, Europe, and Asia.