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Coralline algae are in the order Corallinales, by a containing deposits within its cell walls, giving it . The colors of these are typically some of pink, or another shade of red, but some species can be purple, yellow, blue, white, or gray-green. Typically, these algae grow in a manner ( rocks and other hardscape); in the zone of , and within , these algae appear as an abundance of colorful patches on rock surfaces. Unattached specimens (, ) may form relatively smooth compact balls, or forming to thalli.

The red algae belong to the division , within which the coralline algae form the order Corallinales. There are over 1600 described species of nongeniculate coralline algae.

(1988). 9780198542490, British Museum.
The corallines are presently grouped into two families on the basis of their reproductive structures.
(2025). 9780123739728, Academic Press. .
Most are , though one species lives in ; Pneophyllum cetinaensis.

Coralline algae play an important role in the of coral reefs. , , along with and (both ) feed on coralline algae. In the temperate Mediterranean Sea, coralline algae are the main builders of a typical algal , the Coralligène ("coralligenous").Ballesteros E., 2006 Mediterranean coralligenous assemblages: A synthesis of present knowledge. Oceanography and Marine Biology - an Annual Review 44: 123–130


Description

Forms
Corallines have been divided into two groups based on their , although this division does not conform to :
  • the geniculate (articulated) corallines;
  • the nongeniculate (nonarticulated) corallines.
Geniculate corallines are branching, tree-like organisms which are attached to the substratum by being or possessing , root-like holdfasts. The organisms are made flexible by having non-calcified sections (genicula) separating longer calcified sections (intergenicula). Nongeniculate corallines range from a few micrometres to several centimetres thick crusts. They are often very slow growing, and may occur on rock, coral skeletons, , other algae or (being ). Crusts may be thin and leafy to thick and strongly adherent. Some are parasitic or partly on other corallines. Many coralline crusts produce knobby protuberances ranging from a millimetre to several centimetres high. Some are free-living as (rounded, free-living specimens). The morphological complexity of rhodoliths enhances species diversity, and can be used as a non-taxonomic descriptor for monitoring.


Growth
Corallines, especially encrusting forms, are slow growers, and expand by annually. All corallines begin with a crustose stage; some later become .

The thalli can be divided into three layers: the , and . The epithallus is periodically shed, either in sheets or piecemeal.

Image:Corallina officinalis Helgoland.JPG| Corallina officinalis Image:Lithothamnion sp..jpg| sp. Image:Mesophyllum sp..jpg| sp. Image:Corallinaceae sp..jpg|Unidentified encrusting species Image:Algue corallinale à déterminer.jpg| Image:Algue corallinale à déterminer - 2.jpg| ditto


Mineralogy
Since coralline algae contain calcium carbonate, they fossilize fairly well. They are particularly significant as stratigraphic markers in petroleum geology. Coralline rock was used as building stone since .
(2025). 9783319293134

The calcite crystals composing the cell wall are elongated perpendicular to the cell wall. The calcite normally contains , with the magnesium content varying as a function of species and water temperature. If the proportion of magnesium is high, the deposited mineral is more soluble in ocean water, particularly in colder waters, making some coralline algae deposits more vulnerable to ocean acidification.


Evolutionary history
The of corallines matches their molecular history, and is complete and continuous.

corallines are reported from the Doushantuo formation; later stem-group forms include , Petrophyton, , and Archaeolithophyllum. The corallines were thought to have evolved from within the , a view that has been disputed. True (or ) corallines are found in rocks of Jurassic age onwards.

The crown group corallines have an excellent fossil record from the onwards, consistent with that show the divergence of the modern taxa beginning around this period. The fossil record of nonarticulated forms is better: the unmineralized geniculae of articulated forms break down quickly, scattering the mineralized portions (disarticulation), which then decay more quickly. This said, non-mineralizing coralline algae are known from the of ,Smith, M.R. and Butterfield, N.J. 2013: A new view on Nematothallus: coralline red algae from the Silurian of Gotland. Palaeontology 56, 345–359. 10.1111/j.1475-4983.2012.01203.x and the earliest known coralline deposits date from the , although modern forms radiated in the .

The tend to be more diverse in periods of high ocean temperatures; the opposite is true for the . The group's diversity has closely tracked the efficiency of grazing herbivores; for instance, the appearance of in the marked a spike in coralline diversity, and the extinction of many delicately branched (and thus predation-prone) forms.


Taxonomy
The group's internal taxonomy is in a state of flux; for many years, they were included in the order as the family Corallinaceae until, in 1986, they were raised to the order Corallinales. Molecular studies are proving more reliable than morphological methods in approximating relationships within the group. Recent advances in morphological classification based on skeletal , however, are promising. Crystal morphology within the calcified cell wall of coralline algae was found to have a high correspondence with molecular studies. These skeletal structures thus provide morphological evidence for molecular relationships within the group.

According to :

According to the World Register of Marine Species:

According to :


Habitat
Coralline algae are widespread in all of the world's oceans, where they often cover close to 100% of rocky . Corallines live in varying depths of water, ranging from where they are periodically to water depth (near the maximum penetration of sunlight in water, within the ). Some species can tolerate brackish or hypersaline waters, and only one strictly freshwater coralline species exists; Pneophyllum cetinaensis, whose ancestor lived in , and was already adapted to and rapid changes in and temperature. (Some species of the morphologically similar, but non-calcifying, , however, can survive in freshwater.) A wide range of and can be tolerated.


Biology
Fresh surfaces are generally colonized by thin crusts of coralline algae, which are replaced by thicker or branched forms during succession over the course of one (in the tropics) to ten (in the Arctic) years. However, the transition from crusts to branched form depends on environmental conditions. Crusts may also become detached and form calcareous nodules known as .
(2025). 9783319293134
Their growth may be also disrupted by local environmental factors. While coralline algae are present in most hard substrate marine communities in photic depths, they are more common in higher latitudes and in the Mediterranean. Their ability to calcify in low light conditions makes them the some of deepest photosynthetic multicellular organisms in the ocean, having been found as deep as , Deep-water plant communities from an uncharted seamount off San Salvador Island, Bahamas: distribution, abundance, and primary productivity and as such a critical base of mesophotic ecological systems.


Ecology
Many corallines produce chemicals which promote the settlement of the of certain , particularly . Larval settlement is adaptive for the corallines because the herbivores remove epiphytes which might otherwise smother the crusts and preempt available light. Settlement is also important for ; corallines appear to enhance larval metamorphosis and the survival of larvae through the critical settlement period. It also has significance at the community level; the presence of herbivores associated with corallines can generate patchiness in the survival of young stages of dominant seaweeds. This has been seen this in eastern , and it is suspected the same phenomenon occurs on , yet nothing is known about the herbivore enhancement role of Indo-Pacific corallines, or whether this phenomenon is important in coral reef communities.

Some coralline algae develop into thick crusts which provide for many invertebrates. For example, off eastern , Morton found juvenile , , and suffer nearly 100% mortality due to fish predation unless they are protected by knobby and undercut coralline algae. This is probably an important factor affecting the distribution and grazing effects of herbivores within marine communities. Nothing is known about the microhabitat role of Indo-Pacific corallines. However, the most common species in the region, Hydrolithon onkodes, often forms an intimate relationship with the chiton Cryptoplax larvaeformis. The chiton lives in burrows it makes in H. onkodes plants, and comes out at night to graze on the surface of the coralline. This combination of grazing and burrowing results in a peculiar growth form (called "castles") in H. onkodes, in which the coralline produces nearly vertical, irregularly curved lamellae. Coralline algae are part of the diet of ( Colobocentrotus atratus).

Nongeniculate corallines are of particular significance in the ecology of coral reefs, where they add calcareous material to the structure of the reef, help cement the reef together, and are important sources of primary production. Coralline algae are especially important in reef construction, as they lay down calcium carbonate as calcite. Although they contribute considerable bulk to the calcium carbonate structure of coral reefs, their more important role in most areas of the reef, is in acting as the cement which binds the reef materials into a sturdy structure.Caragnano et al., 2009. 3-D distribution of nongeniculate corallinales: A case study from a reef crest of South Sinai (Red Sea, Egypt). Coral Reefs 28: 881–891

Corallines are particularly important in constructing the algal ridge's reef framework for surf-pounded reefs in both the and Indo-Pacific regions. Algal ridges are carbonate frameworks constructed mainly by nongeniculate coralline algae (after Adey, 1978). They require high and persistent wave action to form, so develop best on windward reefs with little or no seasonal change in wind direction. Algal ridges are one of the main reef structures that prevent oceanic waves from striking adjacent , helping to prevent .


Sloughing
As sessile encrusting organisms, the corallines are prone to being overgrown by other "fouling" algae. The group have many defences to such immuration, most of which depend on waves disturbing their thalli. However, the most relied-upon method involves waiting for herbivores to devour the potential encrusters. This places them in the unusual position of requiring herbivory, rather than benefiting from its avoidance. Many species periodically slough their surface – and anything attached to it, which in a few cases may be an antifouling mechanism serving the same function as enhancing herbivore recruitment. This also affects the community, as many algae recruit on the surface of a sloughing coralline, and are then lost with the surface layer of cells. This can also generate patchiness within the community. The common Indo-Pacific corallines, Neogoniolithon fosliei and Sporolithon ptychoides, slough epithallial cells in continuous sheets which often lie on the surface of the plants.

Not all sloughing serves an antifouling function. Epithallial shedding in most corallines is probably simply a means of getting rid of damaged cells whose metabolic function has become impaired. Morton and his students studied sloughing in the South African intertidal coralline alga, , a species which sloughs up to 50% of its thickness twice a year. This deep-layer sloughing, which is energetically costly, does not affect seaweed recruitment when herbivores are removed. The surface of these plants is usually kept clean by herbivores, particularly the pear limpet, . Sloughing in this case is probably a means of eliminating old reproductive structures and grazer-damaged surface cells, and reducing the likelihood of surface penetration by burrowing organisms.


Relation to humans
The first coralline alga recognized as a living organism was probably in the 1st century AD.
(1994). 9780113100163, Her Majesty's Stationery Office.
In 1837, Rodolfo Amando Philippi recognized coralline were not animals, and he proposed the two generic names and as Lithothamnium.


Economic importance
Because of their calcified structure, coralline algae have a number of economic uses.

Harvesting of maërl beds off the coast of occurs. These beds, spanning several thousand kilometres, contain as-yet undetermined species belonging to the genera Lithothamnion and Lithophyllum.


Soil conditioning
The collection of unattached corallines (maërl) for use as soil conditioners dates to the 18th century. This is particularly significant in and , where more than of calcareum ( Pallas, Adey & McKinnin) and corallioides are dredged annually.


Medicine and food
The earliest use of corallines in medicine involved the preparation of a from ground geniculate corallines of the genera Corallina and Jania. This use stopped towards the end of the 18th century. Medical science now uses corallines in the preparation of , where cell fusion provides the matrix for the regeneration of bone tissue.

Maërl is also used as a food additive for and , as well as in the filtration of acidic drinking water.


Aquaria
As a colorful component of sold in the trade, and an important part of reef health, coralline algae are desired in home aquariums for their aesthetic qualities, and ostensible benefit to the tank ecosystem.


See also
  • Leptofauchea coralligena
  • List of coralline algae species in the British Isles


Further reading

External links

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