dcsimg
Image of Membranipora de Blainville 1830
Creatures » » Animal » » Moss Animals » » Membraniporidae »

Marine Bryozoan

Membranipora membranacea (Linnaeus 1767)

Associations

provided by BioImages, the virtual fieldguide, UK
Plant / epiphyte
Membranipora membranacea grows on frond of Laminaria
Other: major host/prey

Plant / epiphyte
Membranipora membranacea grows on Fucus serratus
Other: unusual host/prey

Plant / epiphyte
Membranipora membranacea grows on Seaweeds
Other: sole host/prey

license
cc-by-nc-sa-3.0
copyright
BioImages
project
BioImages

Look Alikes

provided by Invertebrates of the Salish Sea
How to Distinguish from Similar Species: Although Conopeum reticulum also grows as thin, flat crusts with rectangular zooids and no avicularia, the walls between zooecia are heavily calcified and granular. The California spiral-tufted bryozoan, Bugula californica, may also grow on kelp blades but it does not form a crust.
license
cc-by-nc-sa
copyright
Rosario Beach Marine Laboratory

Habitat

provided by Invertebrates of the Salish Sea
Usually on kelp fronds. May also be on floats or rocks.
license
cc-by-nc-sa
copyright
Rosario Beach Marine Laboratory

Distribution

provided by Invertebrates of the Salish Sea
Geographical Range: All world temperate zones. In the Eastern Pacific, from Alaska to Baja California. It is apparently not native in the North Atlantic.
license
cc-by-nc-sa
copyright
Rosario Beach Marine Laboratory

Habitat

provided by Invertebrates of the Salish Sea
Depth Range: Intertidal to shallow subtidal
license
cc-by-nc-sa
copyright
Rosario Beach Marine Laboratory

Comprehensive Description

provided by Invertebrates of the Salish Sea
This bryozoan frequently grows as thin, flat white crusts on large kelp. The zooids are small rectangular boxlike structures. Most of the frontal of the zooid is membranous instead of calcified, and they have an operculum. They have no distinct spines, though there are knoblike or small spinelike protuberances on the margins between zooids. They have no avicularia or vibracula. The side walls between zooids are thin and not heavily calcified, though they may be slightly serrated. Colonies are often nearly circular and usually nearly white. The individual zooids are little calcified and almost clear.
license
cc-by-nc-sa
copyright
Rosario Beach Marine Laboratory

Comprehensive Description

provided by Invertebrates of the Salish Sea
Biology/Natural History: Bryozoans start from a single individual zooid which repeatedly reproduces asexually to form a colony. In this species, the oldest individual is in the middle. Colonies of this species usually begin to be noticeable in late spring and grow through summer into fall. By fall they may form extensive crusts on the kelp and many colonies have merged with one another. In many bryozoans there are various types of zooids but in this species there is only one type of zooid which serves for feeding, for reproduction, and for defense. The colony appears to be a simultaneous hermaphrodite, or male zooids may develop first. They do not brood their young. Eggs are fertilized then released, and quickly develop into cyphonautes larvae which may feed and develop as plankton for several months. The larvae settle when they encounter kelp such as Laminaria or water with an excess of potassium ions. The small white nudibranch Doridella steinbergae may be found living and feeding on these colonies but it blends in so well it is difficult to see. Other predators include sea urchins and the nudibranch Corambe pacifica. Colonies which have recently been attacked by nudibranchs may grow large chitonous spines, especially on the peripheral zooids. This species appears to be able to feed at higher water flow velocities than some other species can. They frequently encrust the brown kelp Nereocystis luetkeana, and the larvae show a strong preference to settling on that alga over the red alga Mazzaella splendens. The Matson et al. article includes online several videos showing larval settlement in flow.
license
cc-by-nc-sa
copyright
Rosario Beach Marine Laboratory

Membranipora membranacea

provided by wikipedia EN

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,[1] sea-mat or lacy crust bryozoan and is often abundantly found encrusting seaweeds, particularly kelps.[2]

Distribution

Northeast Atlantic including the Baltic Sea, English Channel, Mediterranean Sea and North Sea. Also native to the North Pacific coastline of North America from Alaska to California.[3][4] The species was first recorded on the Atlantic coastline of the U.S. in 1987 in the Gulf of Maine.[5] In Canada's Atlantic coast, it was first observed in Nova Scotia during the early 1990s, and had reached Newfoundland and Labrador by 2002.[1] It now commonly occurs along the Northwest Atlantic from Long Island Sound to northern Newfoundland, including coastal Quebec, New Brunswick, and Prince Edward Island.[1]

Morphology and physiology

Membranipora membranacea colonies consist of individual organisms called zooids, each with a chitinous exoskeleton which is secreted by the epidermis.[6] This exoskeleton, hardened with calcium carbonate, is known as the zooecium, which not only serves to protect the internal structures of the organism, but also keeps the individual permanently attached to the substrate and neighboring zooids.[7] Zooids within a colony can communicate via pores in their interconnecting walls, through which coelomic fluid can be exchanged.[6]

The internal, living portion of the zooid is known as the polypide, whose walls are formed by the outer epidermis and inner peritoneum.[7] The lophophore, a ring of ciliated tentacles, protrudes from the polypide to feed.[8] When not feeding, the lophophore retracts into the polypide through the tentacular sheath. The lophophore is controlled by the zooid's nervous system, which consists of a ganglion at the lophophore base. This ganglion is responsible for motor and sensory impulses to and from the lophophore, as well as the epithelium and digestive tract. The lophophore retractor is the muscle which controls the movement of the lophophore.[7]

This species does not have the ovicells or avicularia seen in most other members of this phylum.

Natural history

Life cycle

Membranipora membranacea begins its life cycle as a plankton-feeding larva, triangular in shape.[6] After several weeks, the larva attach to a substrate and undergo metamorphosis.[9] The larvae typically settle on their preferred substrates in May, and then the colony undergoes growth, stasis and reproduction, shrinkage, and senescence around September, except in regions where temperature allows them to persist further into the winter.[9] The presence of conspecifics may cause a colony to stop growing and begin stasis and reproduction early.[9] The presence of predators also reduces growth of a colony.

Reproduction

Colonies of M. membranacea are protandrous sequential hermaphrodites, where colonies transition from male to female reproductive stages, allowing fertilization to occur between colonies or within colonies.[9] Fertilization takes places in the coelomic fluid of female colonies, and the eggs are released through an opening in the lophophore known as the coelomophore.[6] Reproduction or growth of the colony can also take place by budding in a radial pattern from the first established zooid, the ancestrula.[6]

Ecology

Habitat

M. membranacea prefers shallow marine habitats between the mid intertidal to the shallow sublittoral. It may also be found in brackish water.[2] It is typically found attached in colonies to seaweed, shells, or artificial substrates.[7]

Feeding

M. membranacea can eat food particles such as bacteria, flagellates, diatoms, and other small, planktonic organisms by extracting them from the water with their lophophore.[8] They can also supplement their diet with dissolved organic nutrients through the absorptive epidermis.[8]

Predation

Nudibranchs or sea slugs are the primary predators of M. membranacea. To defend themselves against these predators, the M. membranacea produce chitinous spines which protrude from the corners of the zooid. These spines make it difficult for the nudibranchs to access the polypide of the zooid. However, the energy and resources needed to produce the spines may result in decreased growth and reproduction of the colony.[10]

Ecological significance

M. membranacea on a kelp blade

M. membranacea has become an invasive species in many places, and is believed to have a potentially negative impact on marine ecosystems by limiting the ability of seaweeds to reproduce, specifically by interfering with spore release from the kelp blade. The colonies of this bryozoan are also known to interrupt nutrient uptake by seaweed.[11]

M. membranacea also decreases density and size of kelp plants within kelp beds[5] by increasing tissue loss and blade breakage.[12] Additionally, M. membranacea also affects photosynthetic processes in kelp, since their encrustations may result in reduced concentrations of the primary and accessory pigments in the kelp blade tissue.[12]

References

  1. ^ a b c "Coffin Box Bryozoan". Fisheries and Oceans Canada. 2019-04-09. Retrieved 2022-06-22.
  2. ^ a b Barnes, R.D. (1982). Coasts and Estuaries pp 114-115. Hodder & Staughton, London.
  3. ^ De Haas, W. and F. Knorr (1966). Marine Life pp 212-213. Burke, London.
  4. ^ North, W.J. (1976). Underwater California pp 161. University of California Press. ISBN 0-520-03025-7
  5. ^ a b Lambert, W.J., P.S. Levin and J. Berman (1992). Changes in the structure of a New England (USA) kelp bed: the effects of an introduced species? Marine Ecology Progress Series 88:303-307.
  6. ^ a b c d e Barnes, R.D. (1974). Invertebrate Zoology, 3rd ed. Saunders, Philadelphia, PA:695-712.
  7. ^ a b c d Wilmoth, J.H. (1967). Biology of invertebrata. Prentice-Hall, Englewood Cliffs, NJ:381-384.
  8. ^ a b c De Burgh, M.E. and P.V. Fankboner (1978). A nutritional association between the bull kelp Nereocystis luetkeana and its epizooic bryozoan Membranipora membranacea. Oikos 31(1):69-72.
  9. ^ a b c d Harvell, C.D., H. Caswell and P. Simpson (1990). Density effects in a colonial monoculture: experimental studies with a marine bryozoan (Membranipora membranacea L.). Oecologia 82(2):227-237.
  10. ^ Yoshioka, P.M. (1982). Predator induced polymorphism in the bryozoan Membranipora membranacea (L.). Journal of Experimental Marine Biology and Ecology 61(3):233-242.
  11. ^ Saier, B. and A. S. Chapman (2004). Crusts of the alien bryozoan Membranipora membranacea can negatively impact spore output from native kelps (Laminaria longicruris). Botanica Marina 47(4): 265-271.
  12. ^ a b Hepburn, C.D., C.L. Hurd and R.D. Frew (2006). Colony structure and seasonal differences in light and nitrogen modify the impact of sessile epifauna on the giant kelp Macrocystis pyrifera (L.) C Agardh. Hydrobiologia 560:373-384.
license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN

Membranipora membranacea: Brief Summary

provided by wikipedia EN

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.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN

Description

provided by World Register of Marine Species
De kolonie vormt een uitgebreide, leerachtige bedekking op bruinwieren. Zoïden rechthoekig, met knobbeltjes of korte stekels, waarvan de top niet verkalkt is, op de hoeken. Het membraan bedekt het gehele frontale vlak. Kolonie flexibel, zodat ze zich kan vasthechten aan zeewier zoals Laminaria, zonder te breken als de bladeren bewegen in de golven. « Torenzoïden » waar het frontale membraan opwaarts gericht is als een buis, kunnen aanwezig zijn. Polypide met ongeveer 17 tentakels.

Reference

De_blauwe, H. (2009). Mosdiertjes van de Zuidelijke Bocht van de Noordzee: Determinatiewerk voor België en Nederland. Vlaams Instituut voor de Zee, Oostende. 464.

license
cc-by-4.0
copyright
WoRMS Editorial Board
contributor
De Blauwe, Hans, H.

Distribution

provided by World Register of Marine Species
Membranipora membranacea komt voor als uitgebreide kolonies op bladeren van Laminaria en kleinere kolonies op Fucus serratus

Reference

De_blauwe, H. (2009). Mosdiertjes van de Zuidelijke Bocht van de Noordzee: Determinatiewerk voor België en Nederland. Vlaams Instituut voor de Zee, Oostende. 464.

license
cc-by-4.0
copyright
WoRMS Editorial Board
contributor
De Blauwe, Hans, H.

Distribution

provided by World Register of Marine Species
Leeft enkel op bruinwieren. In België aangespoeld op knotswier, riemwiervoetjes en Laminaria. Alle gereviseerde kolonies in de collectie van het KBIN bleken andere soorten te zijn! Bijgevolg kan M. membranacea niet als inheems in België beschouwd worden. Kwam (komt?) in de Oosterschelde voor van Colijnsplaat tot Yerseke (Faasse & De Blauwe, 2004). Spoelt langs de gehele kust van Nederland aan op zeewier (Lacourt (1978), de Ruijter (2007, 2008)).

References

  • Lacourt, A.W. (1978). De Nederlandse mariene mosdiertjes: Bryozoa (Ectoprocta, Gymnolaemata) [Dutch marine Bryozoa (Ectoprocta, Gymnolaemata)]. Wetenschappelijke Mededeling KNNV, 129. KNNV/Strandwerkgemeenschap: Hoogwoud, The Netherlands. 21 pp.
  • De_blauwe, H. (2009). Mosdiertjes van de Zuidelijke Bocht van de Noordzee: Determinatiewerk voor België en Nederland. Vlaams Instituut voor de Zee, Oostende. 464.
  • Faasse, M.A. & De Blauwe, H. (2004). Faunistisch overzicht van de mariene mosdiertjes van Nederland (Bryozoa: Stenolaemata, Gymnolaemata). Nederlandse Faunistische Mededelingen 21: 17-54.
  • de Ruijter, R. (2007). CS-verslag. Het Zeepaard 67(2): 34-38.
  • de Ruijter, R. (2008). CS-verslag. Het Zeepaard 68(2): 38-43.

license
cc-by-4.0
copyright
WoRMS Editorial Board
contributor
De Blauwe, Hans, H.