Clownfish or anemonefish are fishes from the subfamily Amphiprioninae in the family Pomacentridae. Thirty species of clownfish are recognized: one in the genus Premnas, while the remaining are in the genus Amphiprion. In the wild, they all form symbioticmutualisms with sea anemones. Depending on the species, anemonefish are overall yellow, orange, or a reddish or blackish color, and many show white bars or patches. The largest can reach a length of 17cm (6+1⁄2in), while the smallest barely achieve 7–8cm (2+3⁄4–3+1⁄4in).
Anemonefish are endemic to the warmer waters of the Indian Ocean, including the Red Sea, and Pacific Ocean, the Great Barrier Reef, Hawaii, USA, North America, Southeast Asia, Japan, and the Indo-Malaysian region. While most species have restricted distributions, others are widespread. Anemonefish typically live at the bottom of shallow seas in sheltered reefs or in shallow lagoons. No anemonefish are found in the Atlantic.[1]
Anemonefish are omnivorous and can feed on undigested food from their host anemones, and the fecal matter from the anemonefish provides nutrients to the sea anemone. Anemonefish primarily feed on small zooplankton from the water column, such as copepods and tunicate larvae, with a small portion of their diet coming from algae, with the exception of Amphiprion perideraion, which primarily feeds on algae.[2][3]
Symbiosis and mutualism
Anemonefish and sea anemones have a symbiotic, mutualistic relationship, each providing many benefits to the other. The individual species are generally highly host specific. The sea anemone protects the anemonefish from predators, as well as providing food through the scraps left from the anemone's meals and occasional dead anemone tentacles, and functions as a safe nest site. In return, the anemonefish defends the anemone from its predators and parasites.[4][5] The anemone also picks up nutrients from the anemonefish's excrement.[6] The nitrogen excreted from anemonefish increases the number of algae incorporated into the tissue of their hosts, which aids the anemone in tissue growth and regeneration.[3] The activity of the anemonefish results in greater water circulation around the sea anemone,[7] and it has been suggested that their bright coloring might lure small fish to the anemone, which then catches them.[8] Studies on anemonefish have found that they alter the flow of water around sea anemone tentacles by certain behaviors and movements such as "wedging" and "switching". Aeration of the host anemone tentacles allows for benefits to the metabolism of both partners, mainly by increasing anemone body size and both anemonefish and anemone respiration.[9]
Bleaching of the host anemone can occur when warm temperatures cause a reduction in algal symbionts within the anemone. Bleaching of the host can cause a short-term increase in the metabolic rate of resident anemonefish, probably as a result of acute stress.[10] Over time, however, there appears to be a down-regulation of metabolism and a reduced growth rate for fish associated with bleached anemones. These effects may stem from reduced food availability (e.g. anemone waste products, symbiotic algae) for the anemonefish.[11]
Several theories are given about how they can survive the sea anemone venom:
The mucus coating of the fish may be based on sugars rather than proteins. This would mean that anemones fail to recognize the fish as a potential food source and do not fire their nematocysts, or sting organelles.
The coevolution of certain species of anemonefish with specific anemone host species may have allowed the fish to evolve an immunity to the nematocysts and toxins of their hosts. Amphiprion percula may develop resistance to the toxin from Heteractis magnifica, but it is not totally protected since it was shown experimentally to die when its skin, devoid of mucus, was exposed to the nematocysts of its host.[12]
In a group of anemonefish, a strict dominance hierarchy exists. The largest and most aggressive female is found at the top. Only two anemonefish, a male and a female, in a group reproduce – through external fertilization. Anemonefish are protandrous sequential hermaphrodites, meaning they develop into males first, and when they mature, they become females. If the female anemonefish is removed from the group, such as by death, one of the largest and most dominant males becomes a female.[16] The remaining males move up a rank in the hierarchy. Clownfish live in a hierarchy, like hyenas, except smaller and based on size not sex, and order of joining/birth.[citation needed]
Anemonefish lay eggs on any flat surface close to their host anemones. In the wild, anemonefish spawn around the time of the full moon. Depending on the species, they can lay hundreds or thousands of eggs. The male parent guards the eggs until they hatch about 6–10 days later, typically two hours after dusk.[17]
Anemonefish colonies usually consist of the reproductive male and female and a few male juveniles, which help tend the colony.[18] Although multiple males cohabit an environment with a single female, polygamy does not occur and only the adult pair exhibits reproductive behavior. However, if the female dies, the social hierarchy shifts with the breeding male exhibiting protandrous sex reversal to become the breeding female. The largest juvenile then becomes the new breeding male after a period of rapid growth.[19] The existence of protandry in anemonefish may rest on the case that nonbreeders modulate their phenotype in a way that causes breeders to tolerate them. This strategy prevents conflict by reducing competition between males for one female. For example, by purposefully modifying their growth rate to remain small and submissive, the juveniles in a colony present no threat to the fitness of the adult male, thereby protecting themselves from being evicted by the dominant fish.[20]
The reproductive cycle of anemonefish is often correlated with the lunar cycle. Rates of spawning for anemonefish peak around the first and third quarters of the moon. The timing of this spawn means that the eggs hatch around the full moon or new moon periods. One explanation for this lunar clock is that spring tides produce the highest tides during full or new moons. Nocturnal hatching during high tide may reduce predation by allowing for a greater capacity for escape. Namely, the stronger currents and greater water volume during high tide protect the hatchlings by effectively sweeping them to safety. Before spawning, anemonefish exhibit increased rates of anemone and substrate biting, which help prepare and clean the nest for the spawn.[19]
Before making the clutch, the parents often clear an oval-shaped clutch varying in diameter for the spawn. Fecundity, or reproductive rate, of the females, usually ranges from 600 to 1,500 eggs depending on her size. In contrast to most animal species, the female only occasionally takes responsibility for the eggs, with males expending most of the time and effort. Male anemonefish care for their eggs by fanning and guarding them for 6 to 10 days until they hatch. In general, eggs develop more rapidly in a clutch when males fan properly, and fanning represents a crucial mechanism for successfully developing eggs. This suggests that males can control the success of hatching an egg clutch by investing different amounts of time and energy toward the eggs. For example, a male could choose to fan less in times of scarcity or fan more in times of abundance. Furthermore, males display increased alertness when guarding more valuable broods, or eggs in which paternity is guaranteed. Females, though, display generally less preference for parental behavior than males. All these suggest that males have increased parental investment towards eggs compared to females.[21]
Clownfish hatchlings undergo development after hatching in regards to both their body size and fins. If maintained at the demanded thermal regulation, clownfish undergo proper development of their fins. Clownfish follow the ensuing order in their fin development "Pectorals < caudal < dorsal = anal < pelvic". The early larval stage is crucial to ensure a healthy progression of growth.[22]
Taxonomy
Historically, anemonefish have been identified by morphological features and color pattern in the field, while in a laboratory, other features such as scalation of the head, tooth shape, and body proportions are used.[2] These features have been used to group species into six complexes: percula, tomato, skunk, clarkii, saddleback, and maroon.[23] As can be seen from the gallery, each of the fish in these complexes has a similar appearance. Genetic analysis has shown that these complexes are not monophyletic groups, particularly the 11 species in the A. clarkii group, where only A. clarkii and A. tricintus are in the same clade, with six species,A . allardiA. bicinctus, A. chagosensis, A. chrosgaster, A. fuscocaudatus, A. latifasciatus, and A. omanensis being in an Indian clade, A. chrysopterus having monospecific lineage, and A. akindynos in the Australian clade with A. mccullochi.[24] Other significant differences are that A. latezonatus also has monospecific lineage, and A. nigripes is in the Indian clade rather than with A. akallopisos, the skunk anemonefish.[25]A. latezonatus is more closely related to A. percula and Premnas biaculeatus than to the saddleback fish with which it was previously grouped.[26][25]
Obligate mutualism was thought to be the key innovation that allowed anemonefish to radiate rapidly, with rapid and convergent morphological changes correlated with the ecological niches offered by the host anemones.[26] The complexity of mitochondrial DNA structure shown by genetic analysis of the Australian clade suggested evolutionary connectivity among samples of A. akindynos and A. mccullochi that the authors theorize was the result of historical hybridization and introgression in the evolutionary past. The two evolutionary groups had individuals of both species detected, thus the species lacked reciprocal monophyly. No shared haplotypes were found between species.[27]
Anemonefish make up approximately 43% of the global marine ornamental trade, and approximately 25% of the global trade comes from fish bred in captivity, while the majority is captured from the wild,[30][31] accounting for decreased densities in exploited areas.[32] Public aquaria and captive-breeding programs are essential to sustain their trade as marine ornamentals, and has recently become economically feasible.[33][34] It is one of a handful of marine ornamentals whose complete lifecycle has been in closed captivity. Members of some anemonefish species, such as the maroon clownfish, become aggressive in captivity; others, like the false percula clownfish, can be kept successfully with other individuals of the same species.[35]
When a sea anemone is not available in an aquarium, the anemonefish may settle in some varieties of soft corals, or large polyp stony corals.[36] Once an anemone or coral has been adopted, the anemonefish will defend it. Anemonefish, however, are not obligately tied to hosts, and can survive alone in captivity.[37][38]
Clownfish sold from captivity make up a very small account (10%) of the total trade of these fishes. Designer Clownfish, scientifically named A. ocellaris are much costlier and obtaining them has disrupted their coral reefs. Their attractive allure, color, and patterning have made them out to be an attractive target in wild trading.[22]
In popular culture
Finding Nemobirthday cakes featuring clownfish are popular.
In DisneyPixar's 2003 film Finding Nemo and its 2016 sequel Finding Dory main characters Nemo, his father Marlin, and his mother Coral are clownfish from the species A. ocellaris.[39] The popularity of anemonefish for aquaria increased following the film's release; it is the first film associated with an increase in the numbers of those captured in the wild.[40]
Notes
↑ Exemplars of A. fuscocaudatus have never been sequenced. The authors hypothetically placed this species in the Indian clade because it is the most parsimonious solution regarding the biogeography of anemonefish species.[24]
1 2 Porat, D.; Chadwick-Furman, N.E. (March 2005). "Effects of anemonefish on giant sea anemones: Ammonium uptake, zooxanthella content and tissue regeneration". Marine and Freshwater Behaviour and Physiology. 38 (1): 43–51. Bibcode:2005MFBP...38...43P. doi:10.1080/10236240500057929. S2CID53051081.
↑ "Clown Anemonefish". Nat Geo Wild: Animals. National Geographic Society. 10 May 2011. Archived from the original on 13 January 2010. Retrieved 19 December 2011.
↑ Buston, P. (2004). "Does the Presence of Non-Breeders Enhance the Fitness of Breeders? An Experimental Analysis in the Clown Anemonefish Amphiprion percula". Behavioral Ecology and Sociobiology. 57 (1): 23–31. Bibcode:2004BEcoS..57...23B. doi:10.1007/s00265-004-0833-2. S2CID24516887.
↑ Stephanie Boyer. "Clown Anemofish". Florida Museum of Natural History. Archived from the original on 28 October 2005. Retrieved 15 September 2013.
1 2 Ross, Robert M. (1978). "Reproductive Behavior of the Anemonefish Amphiprion melanopus on Guam". Copeia. 1978 (1): 103–107. doi:10.2307/1443829. JSTOR1443829.
↑ Buston, Peter (November 2004). "Does the presence of non-breeders enhance the fitness of breeders? An experimental analysis in the clown anemonefish Amphiprion percula". Behavioral Ecology and Sociobiology. 57 (1): 23–31. Bibcode:2004BEcoS..57...23B. doi:10.1007/s00265-004-0833-2. S2CID24516887.
↑ Dhaneesh, K. V.; Vinoth, R.; Ghosh, Swagat; Gopi, M.; Kumar, T. T. Ajith; Balasubramanian, T. (2013). "Hatchery Production of Marine Ornamental Fishes: An Alternate Livelihood Option for the Island Community at Lakshadweep". Climate Change and Island and Coastal Vulnerability. pp.253–265. doi:10.1007/978-94-007-6016-5_17. ISBN978-94-007-6015-8.
↑ Shuman, Craig S.; Hodgson, Gregor; Ambrose, Richard F. (December 2005). "Population impacts of collecting sea anemones and anemonefish for the marine aquarium trade in the Philippines". Coral Reefs. 24 (4): 564–573. Bibcode:2005CorRe..24..564S. doi:10.1007/s00338-005-0027-z. S2CID25027153.
↑ Hall, Heather; Douglas Warmolts (2003). "23". In James C. Cato; Christopher L. Brown (eds.). Marine Ornamental Species: Collection, Culture and Conservation. Wiley-Blackwell. pp.303–326. ISBN978-0-8138-2987-6.
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