Coral reef

As the name implies, coral reefs are made up of coral skeletons from mostly intact coral colonies. As other chemical elements present in corals become incorporated into the calcium carbonate deposits, aragonite is formed. However, shell fragments and the remains of coralline algae such as the green-segmented genus Halimeda can add to the reef's ability to withstand damage from storms and other threats. Such mixtures are visible in structures such as Eniwetok Atoll.[30]

Fringing reef

Fringing reef at Eilat at the southern tip of Israel

A fringing reef, also called a shore reef,[36] is directly attached to a shore,[37] or borders it with an intervening narrow, shallow channel or lagoon.[38] It is the most common reef type.[38] Fringing reefs follow coastlines and can extend for many kilometres.[39] They are usually less than 100 metres wide, but some are hundreds of metres wide.[40] Fringing reefs are initially formed on the shore at the low water level and expand seawards as they grow in size. The final width depends on where the sea bed begins to drop steeply. The surface of the fringe reef generally remains at the same height: just below the waterline. In older fringing reefs, whose outer regions pushed far out into the sea, the inner part is deepened by erosion and eventually forms a lagoon.[41] Fringing reef lagoons can become over 100 metres wide and several metres deep. Like the fringing reef itself, they run parallel to the coast. The fringing reefs of the Red Sea are "some of the best developed in the world" and occur along all its shores except off sandy bays.[42]

Barrier reef

Barrier reefs are separated from a mainland or island shore by a deep channel or lagoon.[38] They resemble the later stages of a fringing reef with its lagoon but differ from the latter mainly in size and origin. Their lagoons can be several kilometres wide and 30 to 70 metres deep. Above all, the offshore outer reef edge formed in open water rather than next to a shoreline. Like an atoll, it is thought that these reefs are formed either as the seabed lowered or sea level rose. Formation takes considerably longer than for a fringing reef, thus barrier reefs are much rarer.

The best known and largest example of a barrier reef is the Australian Great Barrier Reef.[38][43] Other major examples are the Belize Barrier Reef and the New Caledonian Barrier Reef.[43] Barrier reefs are also found on the coasts of Providencia,[43] Mayotte, the Gambier Islands, on the southeast coast of Kalimantan, on parts of the coast of Sulawesi, southeastern New Guinea and the south coast of the Louisiade Archipelago.

Platform reef

Platform reefs, variously called bank or table reefs, can form on the continental shelf, as well as in the open ocean, in fact anywhere where the seabed rises close enough to the surface of the ocean to enable the growth of zooxanthemic, reef-forming corals.[44] Platform reefs are found in the southern Great Barrier Reef, the Swain[45] and Capricorn Group[46] on the continental shelf, about 100–200 km from the coast. Some platform reefs of the northern Mascarenes are several thousand kilometres from the mainland. Unlike fringing and barrier reefs which extend only seaward, platform reefs grow in all directions.[44] They are variable in size, ranging from a few hundred metres to many kilometres across. Their usual shape is oval to elongated. Parts of these reefs can reach the surface and form sandbanks and small islands around which may form fringing reefs. A lagoon may form In the middle of a platform reef.

Platform reefs can be found within atolls. There they are called patch reefs and may reach only a few dozen metres in diameter. Where platform reefs form on an elongated structure, e. g. an old, eroded barrier reef, they can form a linear arrangement. This is the case, for example, on the east coast of the Red Sea near Jeddah. In old platform reefs, the inner part can be so heavily eroded that it forms a pseudo-atoll.[44] These can be distinguished from real atolls only by detailed investigation, possibly including core drilling. Some platform reefs of the Laccadives are U-shaped, due to wind and water flow.

Formation of an atoll according to Charles Darwin

Atolls or atoll reefs are a more or less circular or continuous barrier reef that extends all the way around a lagoon without a central island.[47] They are usually formed from fringing reefs around volcanic islands.[38] Over time, the island erodes away and sinks below sea level.[38] Atolls may also be formed by the sinking of the seabed or rising of the sea level. A ring of reefs results, which enclose a lagoon. Atolls are numerous in the South Pacific, where they usually occur in mid-ocean, for example, in the Caroline Islands, the Cook Islands, French Polynesia, the Marshall Islands and Micronesia.[43]

Atolls are found in the Indian Ocean, for example, in the Maldives, the Chagos Islands, the Seychelles and around Cocos Island.[43] The entire Maldives consist of 26 atolls.[48]

A small atoll in the Maldives

Inhabited cay in the Maldives

• Apron reef – short reef resembling a fringing reef, but more sloped; extending out and downward from a point or peninsular shore. The initial stage of a fringing reef.[36]
• Bank reef – isolated, flat-topped reef larger than a patch reef and usually on mid-shelf regions and linear or semi-circular in shape; a type of platform reef.[43]
• Patch reef – common, isolated, comparatively small reef outcrop, usually within a lagoon or embayment, often circular and surrounded by sand or seagrass. Can be considered as a type of platform reef or as features of fringing reefs, atolls and barrier reefs.[43] The patches may be surrounded by a ring of reduced seagrass cover referred to as a grazing halo.[49]
• Ribbon reef – long, narrow, possibly winding reef, usually associated with an atoll lagoon. Also called a shelf-edge reef or sill reef.[36]
• Habili – reef specific to the Red Sea; does not reach near enough to the surface to cause visible surf; may be a hazard to ships (from the Arabic for "unborn")
• Microatoll – community of species of corals; vertical growth limited by average tidal height; growth morphologies offer a low-resolution record of patterns of sea level change; fossilized remains can be dated using radioactive carbon dating and have been used to reconstruct Holocene sea levels[50]
• Cays – small, low-elevation, sandy islands formed on the surface of coral reefs from eroded material that piles up, forming an area above sea level; can be stabilized by plants to become habitable; occur in tropical environments throughout the Pacific, Atlantic and Indian Oceans (including the Caribbean and on the Great Barrier Reef and Belize Barrier Reef), where they provide habitable and agricultural land
• Seamount or guyot – formed when a coral reef on a volcanic island subsides; tops of seamounts are rounded and guyots are flat; flat tops of guyots, or tablemounts, are due to erosion by waves, winds, and atmospheric processes

Coral polyps do not photosynthesize, but have a symbiotic relationship with microscopic algae (dinoflagellates) of the genus Symbiodinium, commonly referred to as zooxanthellae. These organisms live within the polyps' tissues and provide organic nutrients that nourish the polyp in the form of glucose, glycerol and amino acids.[64] Because of this relationship, coral reefs grow much faster in clear water, which admits more sunlight. Without their symbionts, coral growth would be too slow to form significant reef structures. Corals get up to 90% of their nutrients from their symbionts.[65] In return, as an example of mutualism, the corals shelter the zooxanthellae, averaging one million for every cubic centimeter of coral, and provide a constant supply of the carbon dioxide they need for photosynthesis.

Zooxanthellae, the microscopic algae that lives inside coral, gives it colour and provides it with food through photosynthesis

Close up of polyps arrayed on a coral, waving their tentacles. There can be thousands of polyps on a single coral branch.

Corals are animals and not plants. They can appear like plants because they are sessile and take root on the ocean floor. But unlike plants, corals do not make their own food.[66]

Table coral

The varying pigments in different species of zooxanthellae give them an overall brown or golden-brown appearance and give brown corals their colors. Other pigments such as reds, blues, greens, etc. come from colored proteins made by the coral animals. Coral that loses a large fraction of its zooxanthellae becomes white (or sometimes pastel shades in corals that are pigmented with their own proteins) and is said to be bleached, a condition which, unless corrected, can kill the coral.

There are eight clades of Symbiodinium phylotypes. Most research has been conducted on clades A–D. Each clade contributes their own benefits as well as less compatible attributes to the survival of their coral hosts. Each photosynthetic organism has a specific level of sensitivity to photodamage to compounds needed for survival, such as proteins. Rates of regeneration and replication determine the organism's ability to survive. Phylotype A is found more in the shallow waters. It is able to produce mycosporine-like amino acids that are UV resistant, using a derivative of glycerin to absorb the UV radiation and allowing them to better adapt to warmer water temperatures. In the event of UV or thermal damage, if and when repair occurs, it will increase the likelihood of survival of the host and symbiont. This leads to the idea that, evolutionarily, clade A is more UV resistant and thermally resistant than the other clades.[67]

Clades B and C are found more frequently in deeper water, which may explain their higher vulnerability to increased temperatures. Terrestrial plants that receive less sunlight because they are found in the undergrowth are analogous to clades B, C, and D. Since clades B through D are found at deeper depths, they require an elevated light absorption rate to be able to synthesize as much energy. With elevated absorption rates at UV wavelengths, these phylotypes are more prone to coral bleaching versus the shallow clade A.

Clade D has been observed to be high temperature-tolerant, and has a higher rate of survival than clades B and C during modern bleaching events.[67]

Reefs grow as polyps and other organisms deposit calcium carbonate,[68][69] the basis of coral, as a skeletal structure beneath and around themselves, pushing the coral head's top upwards and outwards.[70] Waves, grazing fish (such as parrotfish), sea urchins, sponges and other forces and organisms act as bioeroders, breaking down coral skeletons into fragments that settle into spaces in the reef structure or form sandy bottoms in associated reef lagoons.

Typical shapes for coral species are named by their resemblance to terrestrial objects such as wrinkled brains, cabbages, table tops, antlers, wire strands and pillars. These shapes can depend on the life history of the coral, like light exposure and wave action,[71] and events such as breakages.[72]

Corals reproduce both sexually and asexually. An individual polyp uses both reproductive modes within its lifetime. Corals reproduce sexually by either internal or external fertilization. The reproductive cells are found on the mesenteries, membranes that radiate inward from the layer of tissue that lines the stomach cavity. Some mature adult corals are hermaphroditic; others are exclusively male or female. A few species change sex as they grow.

Internally fertilized eggs develop in the polyp for a period ranging from days to weeks. Subsequent development produces a tiny larva, known as a planula. Externally fertilized eggs develop during synchronized spawning. Polyps across a reef simultaneously release eggs and sperm into the water en masse. Spawn disperse over a large area. The timing of spawning depends on time of year, water temperature, and tidal and lunar cycles. Spawning is most successful given little variation between high and low tide. The less water movement, the better the chance for fertilization. Ideal timing occurs in the spring. The release of eggs or planula usually occurs at night and is sometimes in phase with the lunar cycle (three to six days after a full moon). The period from release to settlement lasts only a few days, but some planulae can survive afloat for several weeks. During this process, the larvae may use several different cues to find a suitable location for settlement. At long distances sounds from existing reefs are likely important,[73] while at short distances chemical compounds become important.[74] The larvae are vulnerable to predation and environmental conditions. The lucky few planulae that successfully attach to substrate then compete for food and space.

Corraline algae Lithothamnion sp.

Coralline algae are important contributors to reef structure. Although their mineral deposition rates are much slower than corals, they are more tolerant of rough wave-action, and so help to create a protective crust over those parts of the reef subjected to the greatest forces by waves, such as the reef front facing the open ocean. They also strengthen the reef structure by depositing limestone in sheets over the reef surface.

Deep-water cloud sponge

"Sclerosponge" is the descriptive name for all Porifera that build reefs. In the early Cambrian period, Archaeocyatha sponges were the world's first reef-building organisms, and sponges were the only reef-builders until the Ordovician. Sclerosponges still assist corals building modern reefs, but like coralline algae are much slower-growing than corals and their contribution is (usually) minor.

In the northern Pacific Ocean cloud sponges still create deep-water mineral-structures without corals, although the structures are not recognizable from the surface like tropical reefs. They are the only extant organisms known to build reef-like structures in cold water.

Eastern oysters (Crassostrea virginica)

Oyster reefs are dense aggregations of oysters living in colonial communities. Other regionally-specific names for these structures include oyster beds and oyster banks. Oyster larvae require a hard substrate or surface to attach on, which includes the shells of old or dead oysters. Thus reefs can build up over time as new larvae settle on older individuals. Crassostrea virginica were once abundant in Chesapeake Bay and shorelines bordering the Atlantic coastal plain until the late nineteenth century.[76] Ostrea angasi is a species of flat oyster that had also formed large reefs in South Australia.[77]

Hippuritida, an extinct order of bivalves known as rudists, were major reef-building organisms during the Cretaceous. By the mid-Cretaceous, rudists became the dominant tropical reef-builders, becoming more numerous than scleractinian corals. During this period, ocean temperatures and saline levels—which corals are sensitive to—were higher than it is today, which may have contributed to the success of rudist reefs.[78]

Around coral reefs, lagoons fill in with material eroded from the reef and the island. They become havens for marine life, providing protection from waves and storms.

Most importantly, reefs recycle nutrients, which happens much less in the open ocean. In coral reefs and lagoons, producers include phytoplankton, as well as seaweed and coralline algae, especially small types called turf algae, which pass nutrients to corals.[90] The phytoplankton form the base of the food chain and are eaten by fish and crustaceans. Recycling reduces the nutrient inputs needed overall to support the community.[65]

Corals also absorb nutrients, including inorganic nitrogen and phosphorus, directly from water. Many corals extend their tentacles at night to catch zooplankton that pass near. Zooplankton provide the polyp with nitrogen, and the polyp shares some of the nitrogen with the zooxanthellae, which also require this element.[90]

Sponges live in crevices in the reefs. They are efficient filter feeders, and in the Red Sea they consume about 60% of the phytoplankton that drifts by. Sponges eventually excrete nutrients in a form that corals can use.[91]

The roughness of coral surfaces is key to coral survival in agitated waters. Normally, a boundary layer of still water surrounds a submerged object, which acts as a barrier. Waves breaking on the extremely rough edges of corals disrupt the boundary layer, allowing the corals access to passing nutrients. Turbulent water thereby promotes reef growth. Without the access to nutrients brought by rough coral surfaces, even the most effective recycling would not suffice.[92]

Deep nutrient-rich water entering coral reefs through isolated events may have significant effects on temperature and nutrient systems.[93][94] This water movement disrupts the relatively stable thermocline that usually exists between warm shallow water and deeper colder water. Temperature regimes on coral reefs in the Bahamas and Florida are highly variable with temporal scales of minutes to seasons and spatial scales across depths.[95]

Water can pass through coral reefs in various ways, including current rings, surface waves, internal waves and tidal changes.[93][96][97][98] Movement is generally created by tides and wind. As tides interact with varying bathymetry and wind mixes with surface water, internal waves are created. An internal wave is a gravity wave that moves along density stratification within the ocean. When a water parcel encounters a different density it oscillates and creates internal waves.[99] While internal waves generally have a lower frequency than surface waves, they often form as a single wave that breaks into multiple waves as it hits a slope and moves upward.[100] This vertical breakup of internal waves causes significant diapycnal mixing and turbulence.[101][102] Internal waves can act as nutrient pumps, bringing plankton and cool nutrient-rich water to the surface.[93][98][103][104][105][106][107][108][109][110][111]

The irregular structure characteristic of coral reef bathymetry may enhance mixing and produce pockets of cooler water and variable nutrient content.[112] Arrival of cool, nutrient-rich water from depths due to internal waves and tidal bores has been linked to growth rates of suspension feeders and benthic algae[98][111][113] as well as plankton and larval organisms.[98][114] The seaweed Codium isthmocladum reacts to deep water nutrient sources because their tissues have different concentrations of nutrients dependent upon depth.[111] Aggregations of eggs, larval organisms and plankton on reefs respond to deep water intrusions.[105] Similarly, as internal waves and bores move vertically, surface-dwelling larval organisms are carried toward the shore.[114] This has significant biological importance to cascading effects of food chains in coral reef ecosystems and may provide yet another key to unlocking the paradox.

Cyanobacteria provide soluble nitrates via nitrogen fixation.[115]

Coral reefs often depend on surrounding habitats, such as seagrass meadows and mangrove forests, for nutrients. Seagrass and mangroves supply dead plants and animals that are rich in nitrogen and serve to feed fish and animals from the reef by supplying wood and vegetation. Reefs, in turn, protect mangroves and seagrass from waves and produce sediment in which the mangroves and seagrass can root.[55]

Reefs are chronically at risk of algal encroachment. Overfishing and excess nutrient supply from onshore can enable algae to outcompete and kill the coral.[122][123] Increased nutrient levels can be a result of sewage or chemical fertilizer runoff. Runoff can carry nitrogen and phosphorus which promote excess algae growth. Algae can sometimes out-compete the coral for space. The algae can then smother the coral by decreasing the oxygen supply available to the reef.[124] Decreased oxygen levels can slow down calcification rates, weakening the coral and leaving it more susceptible to disease and degradation.[125] Algae inhabit a large percentage of surveyed coral locations.[126] The algal population consists of turf algae, coralline algae and macro algae. Some sea urchins (such as Diadema antillarum) eat these algae and could thus decrease the risk of algal encroachment.

Sponges are essential for the functioning of the coral reef that system. Algae and corals in coral reefs produce organic material. This is filtered through sponges which convert this organic material into small particles which in turn are absorbed by algae and corals.[127]

Over 4,000 species of fish inhabit coral reefs.[5] The reasons for this diversity remain unclear. Hypotheses include the "lottery", in which the first (lucky winner) recruit to a territory is typically able to defend it against latecomers, "competition", in which adults compete for territory, and less-competitive species must be able to survive in poorer habitat, and "predation", in which population size is a function of postsettlement piscivore mortality.[128] Healthy reefs can produce up to 35 tons of fish per square kilometer each year, but damaged reefs produce much less.[129]

Sea urchins, Dotidae and sea slugs eat seaweed. Some species of sea urchins, such as Diadema antillarum, can play a pivotal part in preventing algae from overrunning reefs.[130] Researchers are investigating the use of native collector urchins, Tripneustes gratilla, for their potential as biocontrol agents to mitigate the spread of invasive algae species on coral reefs.[131][132] Nudibranchia and sea anemones eat sponges.

A number of invertebrates, collectively called "cryptofauna," inhabit the coral skeletal substrate itself, either boring into the skeletons (through the process of bioerosion) or living in pre-existing voids and crevices. Animals boring into the rock include sponges, bivalve mollusks, and sipunculans. Those settling on the reef include many other species, particularly crustaceans and polychaete worms.[58]

Coral reef systems provide important habitats for seabird species, some endangered. For example, Midway Atoll in Hawaii supports nearly three million seabirds, including two-thirds (1.5 million) of the global population of Laysan albatross, and one-third of the global population of black-footed albatross.[133] Each seabird species has specific sites on the atoll where they nest. Altogether, 17 species of seabirds live on Midway. The short-tailed albatross is the rarest, with fewer than 2,200 surviving after excessive feather hunting in the late 19th century.[134]

Sea snakes feed exclusively on fish and their eggs.[135][136][137] Marine birds, such as herons, gannets, pelicans and boobies, feed on reef fish. Some land-based reptiles intermittently associate with reefs, such as monitor lizards, the marine crocodile and semiaquatic snakes, such as Laticauda colubrina. Sea turtles, particularly hawksbill sea turtles, feed on sponges.[138][139][140]

• 
  Schooling reef fish
• 
  Caribbean reef squid
• 
  Banded coral shrimp
• 
  Whitetip reef shark
• 
  Green turtle
• 
  Giant clam
• 
  Soft coral, cup coral, sponges and ascidians
• 
  Banded sea krait
• 
  The shell of Latiaxis wormaldi, a coral snail

Coral reefs protect shorelines by absorbing wave energy, and many small islands would not exist without reefs. Coral reefs can reduce wave energy by 97%, helping to prevent loss of life and property damage. Coastlines protected by coral reefs are also more stable in terms of erosion than those without. Reefs can attenuate waves as well as or better than artificial structures designed for coastal defence such as breakwaters.[146] An estimated 197 million people who live both below 10 m elevation and within 50 km of a reef consequently may receive risk reduction benefits from reefs. Restoring reefs is significantly cheaper than building artificial breakwaters in tropical environments. Expected damages from flooding would double, and costs from frequent storms would triple without the topmost meter of reefs. For 100-year storm events, flood damages would increase by 91% to $US 272 billion without the top meter.[147]

About six million tons of fish are taken each year from coral reefs. Well-managed reefs have an average annual yield of 15 tons of seafood per square kilometer. Southeast Asia's coral reef fisheries alone yield about $2.4 billion annually from seafood.[142]

Coral aquaculture, also known as coral farming or coral gardening, is showing promise as a potentially effective tool for restoring coral reefs.[189][190][191] The "gardening" process bypasses the early growth stages of corals when they are most at risk of dying. Coral seeds are grown in nurseries, then replanted on the reef.[192] Coral is farmed by coral farmers whose interests range from reef conservation to increased income. Due to its straight forward process and substantial evidence of the technique having a significant effect on coral reef growth, coral nurseries became the most widespread and arguably the most effective method for coral restoration.[193]

Coral fragments growing on nontoxic concrete

Coral gardens take advantage of a coral's natural ability to fragment and continuing to grow if the fragments are able to anchor themselves onto new substrates. This method was first tested by Baruch Rinkevich[194] in 1995 which found success at the time. By today's standards, coral farming has grown into a variety of different forms, but still has the same goals of cultivating corals. Consequently, coral farming quickly replaced previously used transplantation methods or the act of physically moving sections or whole colonies of corals into a new area.[193] Transplantation has seen success in the past and decades of experiments have led to a high success and survival rate. However, this method still requires the removal of corals from existing reefs. With the current state of reefs, this kind of method should generally be avoided if possible. Saving healthy corals from eroding substrates or reefs that are doomed to collapse could be a major advantage of utilizing transplantation.

Coral gardens generally take on the safe forms no matter where you go. It begins with the establishment of a nursery where operators can observe and care for coral fragments.[193] It goes without saying that nurseries should be established in areas that are going to maximize growth and minimize mortality. Floating offshore coral trees or even aquariums are possible locations where corals can grow. After a location has been determined, collection and cultivation can occur.

The major benefit of using coral farms is it lowers polyp and juvenile mortality rates. By removing predators and recruitment obstacles, corals are able to mature without much hindrance. However, nurseries cannot stop climate stressors. Warming temperatures or hurricanes can still disrupt or even kill nursery corals.

Deep sea corals at the Wagner Seamount. These corals are well adapted to deep water conditions where substrates are plentiful.

Efforts to expand the size and number of coral reefs generally involve supplying substrate to allow more corals to find a home. Substrate materials include discarded vehicle tires, scuttled ships, subway cars and formed concrete, such as reef balls. Reefs grow unaided on marine structures such as oil rigs. In large restoration projects, propagated hermatypic coral on substrate can be secured with metal pins, superglue or milliput. Needle and thread can also attach A-hermatype coral to substrate.

Biorock is a substrate produced by a patented process that runs low voltage electrical currents through seawater to cause dissolved minerals to precipitate onto steel structures. The resultant white carbonate (aragonite) is the same mineral that makes up natural coral reefs. Corals rapidly colonize and grow at accelerated rates on these coated structures. The electrical currents also accelerate the formation and growth of both chemical limestone rock and the skeletons of corals and other shell-bearing organisms, such as oysters. The vicinity of the anode and cathode provides a high-pH environment which inhibits the growth of competitive filamentous and fleshy algae. The increased growth rates fully depend on the accretion activity. Under the influence of the electric field, corals display an increased growth rate, size and density.

Simply having many structures on the ocean floor is not enough to form coral reefs. Restoration projects must consider the complexity of the substrates they are creating for future reefs. Researchers conducted an experiment near Ticao Island in the Philippines in 2013[195] where several substrates in varying complexities were laid in the nearby degraded reefs. Large complexity consisted of plots that had both a man-made substrates of both smooth and rough rocks with a surrounding fence, medium consisted of only the man-made substrates, and small had neither the fence or substrates. After one month, researchers found that there was a positive correlation between structure complexity and recruitment rates of larvae.[195] The medium complexity performed the best with larvae favoring rough rocks over smooth rocks. Following one year of their study, researchers visited the site and found that many of the sites were able to support local fisheries. They came to the conclusion that reef restoration could be done cost-effectively and will yield long term benefits given they are protected and maintained.[195]

One case study with coral reef restoration was conducted on the island of Oahu in Hawaii. The University of Hawaii operates a Coral Reef Assessment and Monitoring Program to help relocate and restore coral reefs in Hawaii. A boat channel from the island of Oahu to the Hawaii Institute of Marine Biology on Coconut Island was overcrowded with coral reefs. Many areas of coral reef patches in the channel had been damaged from past dredging in the channel.

Coral in preparation of being relocated

Dredging covers corals with sand. Coral larvae cannot settle on sand; they can only build on existing reefs or compatible hard surfaces, such as rock or concrete. Because of this, the University decided to relocate some of the coral. They transplanted them with the help of United States Army divers, to a site relatively close to the channel. They observed little if any damage to any of the colonies during transport and no mortality of coral reefs was observed on the transplant site. While attaching the coral to the transplant site, they found that coral placed on hard rock grew well, including on the wires that attached the corals to the site.

No environmental effects were seen from the transplantation process, recreational activities were not decreased, and no scenic areas were affected.

As an alternative to transplanting coral themselves, juvenile fish can also be encouraged to relocate to existing coral reefs by auditory simulation. In damaged sections of the Great Barrier Reef, loudspeakers playing recordings of healthy reef environments were found to attract fish twice as often as equivalent patches where no sound was played, and also increased species biodiversity by 50%.

Another possibility for coral restoration is gene therapy: inoculating coral with genetically modified bacteria, or naturally-occurring heat-tolerant varieties of coral symbiotes, may make it possible to grow corals that are more resistant to climate change and other threats.[196] Warming oceans are forcing corals to adapt to unprecedented temperatures. Those that do not have a tolerance for the elevated temperatures experience coral bleaching and eventually mortality. There is already research that looks to create genetically modified corals that can withstand a warming ocean. Madeleine J. H. van Oppen, James K. Oliver, Hollie M. Putnam, and Ruth D. Gates described four different ways that gradually increase in human intervention to genetically modify corals.[197] These methods focus on altering the genetics of the zooxanthellae within coral rather than the alternative.

The first method is to induce acclimatization of the first generation of corals.[197] The idea is that when adult and offspring corals are exposed to stressors, the zooxanthellae will gain a mutation. This method is based mostly on the chance that the zooxanthellae will acquire the specific trait that will allow it to better survive in warmer waters. The second method focuses on identifying what different kinds of zooxanthellae are within the coral and configuring how much of each zooxanthella lives within the coral at a given age.[197] Use of zooxanthellae from the previous method would only boost success rates for this method. However, this method would only be applicable to younger corals, for now, because previous experiments of manipulation zooxanthellae communities at later life stages have all failed. The third method focuses on selective breeding tactics.[197] Once selected, corals would be reared and exposed to simulated stressors in a laboratory. The last method is to genetically modify the zooxanthellae itself.[197] When preferred mutations are acquired, the genetically modified zooxanthellae will be introduced to an aposymbiotic poly and a new coral will be produced. This method is the most laborious of the fourth, but researchers believe this method should be utilized more and holds the most promise in genetic engineering for coral restoration.

Hawaiian coral reefs smothered by the spread of invasive algae were managed with a two-prong approach: divers manually removed invasive algae, with the support of super-sucker barges. Grazing pressure on invasive algae needed to be increased to prevent the regrowth of the algae. Researchers found that native collector urchins were reasonable candidate grazers for algae biocontrol, to extirpate the remaining invasive algae from the reef.[131]

Students from Nā Pua No‘eau remove invasive algae from Kāne‘ohe Bay. Programs could be created to remove algae from Caribbean reefs

Macroalgae, or better known as seaweed, has to potential to cause reef collapse because they can outcompete many coral species. Macroalgae can overgrow on corals, shade, block recruitment, release biochemicals that can hinder spawning, and potentially form bacteria harmful to corals.[198][199] Historically, algae growth was controlled by herbivorous fish and sea urchins. Parrotfish are a prime example of reef caretakers. Consequently, these two species can be considered as keystone species for reef environments because of their role in protecting reefs.

Before the 1980s, Jamaica's reefs were thriving and well cared for, however, this all changed after Hurricane Allen occurred in 1980 and an unknown disease spread across the Caribbean. In the wake of these events, massive damage was caused to both the reefs and sea urchin population across Jamaican's reefs and into the Caribbean Sea. As little as 2% of the original sea urchin population survived the disease.[199] Primary macroalgae succeeded the destroyed reefs and eventually larger, more resilient macroalgae soon took its place as the dominant organism.[199][200] Parrotfish and other herbivorous fish were few in numbers because of decades of overfishing and bycatch at the time.[200] Historically, the Jamaican coast had 90% coral cover and was reduced to 5% in the 1990s.[200] Eventually, corals were able to recover in areas where sea urchin populations were increasing. Sea urchins were able to feed and multiply and clear off substrates, leaving areas for coral polyps to anchor and mature. However, sea urchin populations are still not recovering as fast as researchers predicted, despite being highly fecundate.[199] It is unknown whether or not the mysterious disease is still present and preventing sea urchin populations from rebounding. Regardless, these areas are slowly recovering with the aid of sea urchin grazing. This event supports an early restoration idea of cultivating and releasing sea urchins into reefs to prevent algal overgrowth.[201][202]

In 2014, Christopher Page, Erinn Muller, and David Vaughan from the International Center for Coral Reef Research & Restoration at Mote Marine Laboratory in Summerland Key, Florida developed a new technology called "microfragmentation," in which they use a specialized diamond band saw to cut corals into 1 cm² fragments instead of 6 cm² to advance the growth of brain, boulder, and star corals.[203] Corals Orbicella faveolata and Montastraea cavernosa were outplanted off the Florida's shores in several microfragment arrays. After two years, O. faveolata had grown 6.5x its original size while M. cavernosa had grown nearly twice its size.[203] Under conventional means, both corals would have required decades to reach the same size. It is suspected that if predation events had not occurred near the beginning of the experiment O. faveolata would have grown at least ten times its original size.[203] By using this method, Mote Marine Laboratory produced 25,000 corals and planted 10,000 in the Florida Keys in only one year. Shortly after, they discovered that these microfragments fused with other microfragments from the same parent coral. Typically, corals that are not from the same parent fight and kill nearby corals in an attempt to survive and expand. This new technology is known as "fusion" and has been shown to grow coral heads in just two years instead of the typical 25–75 years. After fusion occurs, the reef will act as a single organism rather than several independent reefs. Currently, there has been no published research into this method.[203]