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  • Guppy 

    The guppy (Poecilia reticulata), also known as millionfish or the rainbow fish,[3] is one of the world’s most widely distributed tropical fish and one of the most popular freshwater aquarium fish species. It is a member of the family Poeciliidae and, like almost all American members of the family, is live-bearing.[4] Guppies originate from northeast South America, but have been introduced to many environments and are now found all over the world. They are highly adaptable and thrive in many different environmental and ecological conditions.[5] Male guppies, which are smaller than females, have ornamental caudal and dorsal fins. Wild guppies generally feed on a variety of food sources, including benthic algae and aquatic insect larvae.[6] Guppies are used as a model organism in the fields of ecologyevolution, and behavioural studies.[5]

    Taxonomy

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    Guppies were first described in Venezuela as Poecilia reticulata by Wilhelm Peters in 1859 and as Lebistes poecilioides in Barbados by De Filippi in 1861. It was named Girardinus guppii by Albert Günther in honor of Robert John Lechmere Guppy, who sent specimens of the species from Trinidad to the Natural History Museum in London.[7] It was reclassified as Lebistes reticulatus by Regan in 1913. Then in 1963, Rosen and Bailey brought it back to its original name, Poecilia reticulata. While the taxonomy of the species was frequently changed and resulted in many synonyms, “guppy” remains the common name even as Girardinus guppii is now considered a junior synonym of Poecilia reticulata.[5]

    Distribution and habitat

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    Guppies are native to Antigua and BarbudaBarbadosBrazilGuyanaTrinidad and Tobago, and Venezuela.[8][9] However, guppies have been introduced to many different countries on every continent except Antarctica. Sometimes this has occurred accidentally, but most often as a means of mosquito control. The guppies were expected to eat the mosquito larvae and help slow the spread of malaria, but in many cases, these guppies have had a negative impact on native fish populations.[10] Field studies reveal that guppies have colonized almost every freshwater body accessible to them in their natural ranges, especially in the streams located near the coastal fringes of mainland South America. Although not typically found there, guppies also have tolerance to brackish water and have colonized some brackish environments.[5] They tend to be more abundant in smaller streams and pools than in large, deep, or fast-flowing rivers.[11] They also are capable of being acclimated to full saltwater like their molly cousins.

    Description

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    Sexual polymorphism exhibited in the Trinidadian guppy (above male, below female)
    Guppy breeds

    Guppies exhibit sexual dimorphism. While wild-type females are grey in body colour, males have splashes, spots, or stripes that can be any of a wide variety of colors.[12] The development and exhibiting of color patterns in male guppies is usually due to the amount of thyroid hormone that they contain. The thyroid hormones not only influence color pattern, but control endocrine function in response to their environment.[13] The size of guppies vary, but males are typically 1.5–4 cm (0.6–1.6 in) long, while females are 3–7 cm (1.2–2.8 in) long.

    A variety of fancy guppy strains are produced by breeders through selective breeding, characterized by different colours, patterns, shapes, and sizes of fins, such as snakeskin and grass varieties. Many domestic strains have morphological traits that are very distinct from the wild-type antecedents. Males and females of many domestic strains usually have larger body size and are much more lavishly ornamented than their wild-type antecedents.[14]

    Guppies have 23 pairs of chromosomes, including one pair of sex chromosomes, the same number as humans.[15] The genes responsible for male guppies’ ornamentations are Y-chromosome linked and are heritable.[16]

    Lifecycle

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    guppy
    Guppy (female)

    Two generations of guppies per year occur in the wild. Guppies are well developed and capable of independent existence without further parental care by the time they are born. Young guppies school together and perform anti-predator tactics. Brood size is extremely variable, yet some consistent differences exist among populations depending on the predation level and other factors.[5] Females of matching body sizes tend to produce more numerous but smaller-sized offspring in high-predation conditions. Female guppies first produce offspring at 10–20 weeks of age, and they continue to reproduce until 20–34 months of age. Male guppies mature in 7 weeks or less.[5] Total lifespan of guppies in the wild varies greatly, but it is typically around 2 years.[17] Variations in such life historic characteristics of guppies are observed in different populations, indicating that different evolutionary pressures exist.

    Maturity

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    Guppies’ body sizes are positively correlated with age, and their size at maturation varies highly depending on the predation risk of the occupied environments. Male and female guppies from high-predation regions mature faster and start reproducing earlier, and they devote more resources to reproduction than those from low-predation regions.[18] Females from high-predation regions reproduce more frequently and produce more offspring per litter, indicating that they are more fecund than low-predation females. Female guppies’ reproductive success is also related to age. Older females produce offspring with reduced size and at increased interbrood intervals.[19]

    Senescence

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    One major factor that affects wild guppies’ senescence patterns is the mortality rate caused by predation. Guppies from high-predation environments suffer high extrinsic mortality rate because they are more likely to be killed by predators. Female guppies from high-predation environments experience a significant increase in mortality at 6 months of age, while those from low-predation environments do not suffer increased mortality until 16 months. However, guppies from high-predation environments were found to have longer lifespans because their reproductive lifespans are longer. No significant difference is seen in postreproductive lifespans.[17][dubious – discuss]

    Population regulations

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    In addition to senescence pattern, resource availability and density also matter in regulation of guppy populations. Guppies reduce their fecundity and reproductive allocation in response to scarce food. When food is abundant, they increase brood size.[20] Differential reproductive allocation can be the cause of seasonality of life-history characteristics in some guppy populations. For example, during the wet season from May to December, guppies in the Northern Range of Trinidad reduce their investment in reproduction regardless of predation level, possibly in response to decreased food resources.[21] Population density also matters in simpler environments because higher intraspecific competition causes a decrease in reproductive rate and somatic growth rate, and a corresponding increase in juvenile mortality rate due to cannibalism.[22] It was confirmed that in low-predation environments, guppy populations are in part regulated by density.[23]

    Ecology and behavior

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    Mating

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    Guppies have the mating system called polyandry, where females mate with multiple males.[24] Multiple mating is beneficial for males because the males’ reproductive success is directly related to how many times they mate. The cost of multiple mating for males is very low because they do not provide material benefit to the females or parental care to the offspring. Conversely, multiple mating can be disadvantageous for females because it reduces foraging efficiency and increases the chances of predation and parasitic infection.[25] However, females gain some potential benefits from multiple mating. For example, females that mate multiple times are found to be able to produce more offspring in shorter gestation time, and their offspring tend to have better qualities such as enhanced schooling and predator evasion abilities.[25]

    Female guppies mate again more actively and delay the development of a brood when the anticipated second mate is more attractive than the first male. Experiments show that remating females prefer a novel male to the original male or a brother of the original male with similar phenotypes. Females’ preference for novel males in remating can explain the excessive phenotypic polymorphism in male guppies.[26]

    Inbreeding avoidance

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    Inbreeding ordinarily has negative fitness consequences (inbreeding depression), and as a result species have evolved mechanisms to avoid inbreeding. Inbreeding depression is considered to be due largely to the expression of homozygous deleterious recessive mutations.[27] Numerous inbreeding avoidance mechanisms operating prior to mating have been described. However, inbreeding avoidance mechanisms that operate subsequent to copulation are less well known. In guppies, a post-copulatory mechanism of inbreeding avoidance occurs based on competition between sperm of rival males for achieving fertilization.[28] In competitions between sperm from an unrelated male and from a full sibling male, a significant bias in paternity towards the unrelated male was observed.[28]

    Females’ mating choice

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    Female guppy choice plays an important role in multiple mating. Female guppies are attracted to brightly colored males, especially ones with orange spots on the flank.[29] Orange spots can serve as an indicator of better physical fitness, as orange-spotted males are observed to swim longer in a strong current.[30] There is also the concept of color association to possibly explain mate choice since one of the food sources wild guppies compete vigorously for is the fruit of cabrehash trees (Sloanea laurifolia), an orange carotenoid-containing fruit.[31] The orange coloration that female guppies select for in males is composed of carotenoids, the saturation of which is affected by the male’s carotenoid ingestion and parasite load.[32] Guppies cannot synthesize these pigments by themselves and must obtain them through their diet. Because of this connection, females are possibly selecting for healthy males with superior foraging abilities by choosing mates with bright orange carotinoid pigments, thus increasing the survival chance of her offspring.[32] Due to the advantage in mating, male guppies evolve to have more ornamentation across generations in low-predation environments where the cost of being conspicuous is lower. The rate and duration of courtship display of male guppies also play an important role in female guppies’ mating choice. Courtship behavior is another indicator of fitness due to the physical strength involved in maintaining the courtship dance, called sigmoid display, in which the males flex their bodies into an S shape and vibrate rapidly.[33]

    Sigmoid display of male guppy

    Female mating choice may also be influenced by another female’s choice. In an experiment, female guppies watched two males, one solitary and the other actively courting another female, and were given a choice between the two. Most females spent a longer time next to the male that was courting.[34] Female guppies’ preference for fit males allows their descendants to inherit better physical fitness and better chance of survival.

    Predation

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    Aequidens pulcher, a common predator of guppies

    Guppies have many predators, such as larger fish and birds, in their native range. Some of their common predators in the wild are Crenicichla altaAnablepsoides hartii, and Aequidens pulcher.[35] Guppies’ small bodies and the bright coloration of males make them easy prey, and like many fish, they often school together to avoid predation. Schooling is more favored by evolution in populations of guppies under high predation pressure, exerted either by predator type or predator density.[36] Male guppies rely on schooling, in particular the behavioral responses of females, to make antipredator decisions.[37] Coloration of guppies also evolves differentially in response to predation. Male guppies that are brighter in color have an advantage in mating as they attract more females in general, but they have a higher risk of being noticed by predators than duller males. Male guppies evolve to be more dull in color and have fewer, smaller spots under intense predation both in wild and in laboratory settings.[38] Female guppies in a high-predation environment also evolve to prefer brightly colored males less, often rejecting them.[39]

    Predator inspection

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    When guppies encounter a potential predator, some of them approach the predator to assess danger. This behavior, called predator inspection, benefits the inspector since it gains information, but puts the inspector at a risk of predation. To reduce the risk, inspectors avoid the predator’s mouth area—called the ‘attack cone’—and approach the predator from the side or back. They may also form a group for protection, the size of which is larger in high-predation populations. Although evidence indicates predators are less likely to attack an inspector than a non-inspector, the inspectors remain at higher risk due to proximity to the predator.[40]

    Risk-taking behaviors such as predator inspection can be evolutionarily stable only when a mechanism prevents selfish individuals from taking advantage of “altruistic” individuals. Guppies may adopt a conditional-approach strategy that resembles tit for tat. According to this hypothesis, guppies would inspect the predator on the first move, but if their co-inspectors do not participate in the predator inspection visits or do not approach the predator close enough, they can retaliate by copying the defector’s last move in the next predator inspection visit. The hypothesis was supported in laboratory experiments.[41]

    Predator diversion

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    When guppies detect a predator, their irises rapidly darken from silver to jet black, which draws predators to attack the guppies’ head instead of their body’s center of mass.[42][43] Perhaps counterintuitively, this predator divertive behavior allows guppies to rapidly pivot out of the way as predators lunge where the guppies’ head was; this “matador-like” anti-predator behavior was first described in guppies but may be found in other animal species with bright, attention-grabbing coloration located on vital organs, such as epaulette sharks.[43][42]

    Parasites

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    Guppies are also host to a range of parasites and one of these, Gyrodactylus turnbulli, has been used as a model system for studying host-parasite interactions.[44] Recent work on this has shown that the interaction between exposure to chronic anthropogenic noise and G. turnbulli can decrease guppy survival. While a short burst of underwater noise has positive effects on parasite densities on the host. Most likely resulting in negative fitness effects for guppies.[44]

    Feeding

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    Wild guppies feed on algal remains, diatoms, invertebrates, zooplankton, detritus,[45] plant fragments, mineral particles, aquatic insect larvae, and other sources. Algal remains constitute the biggest proportion of wild guppy diet in most cases, but diets vary depending on the specific conditions of food availability in the habitat.[6][46] For example, a study on wild Trinidad guppies showed that guppies collected from an oligotrophic upstream region (upper Aripo River) mainly consumed invertebrates, while guppies from a eutrophic downstream region (lower Tacarigua River) consumed mostly diatoms and mineral particles. Algae are less nutritious than invertebrates, and the guppies that feed mainly on algae have poor diets.[5]

    Guppy food – Daphnia magna

    Guppies have also been observed eating native fishes’ eggs, occasionally expressing cannibalism, also eating its own young, when kept in laboratory conditions.[45]

    Guppies’ diet preference is not simply correlated to the abundance of a particular food. Laboratory experiments confirmed that guppies show ‘diet switching’ behavior, in which they feed disproportionately on the more abundant food when they are offered two food choices. The result shows that different groups of guppies have weak and variable food preference.[47] Diet preference in guppies could be related to factors such as the presence of competitors. For example, the lower Tacarigua River has a larger variety of species and competition for invertebrate prey is higher; therefore, the proportion of invertebrates is small in the diets of those guppies.[5]

    Foraging

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    Guppies often forage in groups because they can find food more easily. Shoaling guppies spend less time and energy on antipredatory behavior than solitary ones and spend more time on feeding. However, such behavior results in food that is found being shared with other members of the group. Studies also show when an evolutionary cost exists, guppies that tend to shoal are less aggressive and less competitive with regards to scarce resources.[48] Therefore, shoaling is preferred in high-predation regions, but not in low-predation regions. When guppies with a high tendency to shoal were isolated from high-predation regions and were relocated to predator-free environments, over time, they decreased their shoaling behavior, supporting the hypothesis that shoaling is less preferred in low-predation environments.[49]

    Reproduction

    [edit]Birth of guppy fry

    A guppy fry in an aquarium at one week of age

    Guppies are highly prolific livebearers.[50] The gestation period of guppies varies considerably, ranging from 20 to 60 days at 25 to 27 C and depending on several environmental factors.[51][52] Reproduction typically continues through the year, and the female becomes ready for conception again quickly after parturition.[5] Male guppies, like other members of the family Poeciliidae, possess a modified tubular anal fin called the gonopodium, located directly behind the ventral fin. The gonopodium has a channel-like structure through which bundles of spermatozoa, called spermatozeugmata, are transferred to females. In courted mating, where the female shows receptive behavior following the male’s courtship display, the male briefly inserts the gonopodium into the female’s genital pore for internal fertilization. However, in the case of sneaky mating where copulation is forced, the male approaches the female and thrusts the gonopodium at the female’s urogenital pore.[53]

    Once inseminated, female guppies can store sperm in their ovaries and gonoducts, which can continue to fertilize ova up to eight months.[54] Because of the sperm-storage mechanism, males are capable of posthumous reproduction, meaning the female mate can give birth to the male’s offspring long after the male’s death, which contributes significantly to the reproductive dynamics of the wild guppy populations.[55]

    The guppy has been successfully hybridised with various species of molly (Poecilia latipinna or P. velifera), e.g., male guppy and female molly. However, the hybrids are always male and appear to be infertile.[56] The guppy has also been hybridised with the Endler’s livebearer (Poecilia wingei) to produce fertile offspring, with the suggestion that, despite physical and behavioural differences, Endler’s may represent a subspecies of Poecilia reticulata rather than a distinct species.[57][58]

    Inbreeding depression

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    Due to the extensive selective breeding of guppies for desirable traits such as greater size and colour, some strains of the fish have become less hardy than their wild counterparts. Immense inbreeding of guppies has been found to affect body size, fertility and susceptibility to diseases.[59]

    In the aquarium

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    Guppy standards

    Large strains:
    A – Veil tail
    B – Triangle tail
    C – Fan tail
    D – Flag tail

    Sword strains:
    E – Double sword
    F – Upper sword
    G – Lower sword
    H – Lyre tail

    Short strains:
    I – Spade tail
    J – Spear tail
    K – Round tail
    L – Pin tail

    Guppies prefer a hard-water aquarium with a temperature between 25.5 and 27.8 °C (78 and 82 °F) and salt levels equivalent to one tablespoon per 19 L (5 US gal).[60] They can withstand levels of salinity up to 150% that of normal seawater,[61] which has led to them being occasionally included in marine tropical community tanks, as well as in freshwater tropical tanks. Guppies are generally peaceful, though nipping behaviour is sometimes exhibited between male guppies or towards other top swimmers like members of the genus Xiphophorus (platies and swordtails), and occasionally other fish with prominent fins, such as angelfish. Guppies should not be kept as a single fish in an aquarium because both males and females show signs of shoaling, and are usually found in large groups in the wild.[62] Its most famous characteristic is its propensity for breeding, and it can breed in both freshwater and marine aquaria.[63]

    Guppies prefer water temperatures around 22.2–26.1 °C (72–79 °F) for reproduction. Pregnant female guppies have enlarged and darkened gravid spots near their anal vents. Just before birth, the eyes of fry may be seen through the translucent skin in this area of the female’s body.[64] When birth occurs, individual offspring are dropped in sequence, typically over a period of one to six hours. The female guppy has drops of two to 200 fry at a time, though typically ranging between 30 and 60.[65]

    Well-fed adults do not often eat their own young, although sometimes safe zones are required for the fry. Specially designed livebearer birthing tanks, which can be suspended inside the aquarium, are available from aquatic retailers. These also serve to shield the pregnant female from further attention from the males, which is important because the males sometimes attack the females while they are giving birth.[66] It also provides a separate area for the newborn young as protection from being eaten by their mother.[67] However, if a female is put in the breeder box too early, it may cause her to have a miscarriage. Well-planted tanks that offer barriers to adult guppies shelter the young quite well. Guppy grasswater spritewater wisteriaduckweedwater lettuce and java moss are all good choices. A continuous supply of live food, such as Daphnia or brine shrimp, keep adult fish full and may spare the fry when they are born.[68] Young fry take roughly three or four months to reach maturity. Feeding fry live foods, such as baby brine shrimpmicrowormsinfusoria and vinegar eels, is recommended. Alternatives include finely ground flake food, egg yolk, and liquid fish food, though the particulates in these may be too large for the youngest fry to eat.[69]

    Common diseases

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    Guppies are susceptible to various diseases, which may stem from bacterial, parasitic, or fungal infections. Maintaining a clean tank, a balanced diet, and regular monitoring can help in preventing these diseases.

    Ichthyophthirius multifiliis (Ich)

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    Ichthyophthirius multifiliis, commonly known as ich, is a protozoan parasite that infects guppies and other freshwater fish. The infection is characterized by white cysts appearing on the skin, gills, and fins of the affected fish, giving a distinct white spot appearance which is often referred to as “white spot disease”.[70]

    The life cycle of Ichthyophthirius multifiliis involves three stages: the trophont stage, the tomont stage, and the theront stage.

    Fin rot

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    Fin rot is primarily caused by bacterial infections, although fungal infections can also be a culprit. The condition manifests through the progressive decay or fraying of the fins, often accompanied by discoloration, usually turning the edges of the fins white, black, or red. The primary causative agents of fin rot are gram-negative bacteria such as Pseudomonas fluorescens and Aeromonas hydrophila.[71] Poor water quality, overcrowding, and stress are significant contributors to the onset and progression of the disease, as they create an environment conducive for bacterial growth and can compromise the fish’s immune system.[72]

    Columnaris

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    Columnaris, also known as cotton mouth disease or cotton wool disease, is a common bacterial infection in guppies and other freshwater fish, caused by the bacterium Flavobacterium columnare. This bacterium thrives in warm, freshwater environments. Treatment for columnaris should commence promptly to prevent severe mortality. Common treatment measures include: improving water quality, antibacterial medications such as kanamycinerythromycin, or oxytetracycline, and in extreme cases, antibiotic injections.[73][74]

    Velvet disease

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    Velvet, also known as gold dust disease, is a prevalent ailment caused by the dinoflagellate parasites of the genus Oodinium.[75] When these parasites attach to a fish’s skin, gills, and eyes, they trigger a range of symptoms. Notable symptoms include a fine gold or rust-colored dust appearing on the fish’s body, clamped fins, scratching against objects, rapid gill movement due to irritation, decreased feeding, lethargy, and, in advanced stages, respiratory distress.

    Swim bladder disease

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    Swim bladder disease is a common condition which impairs their ability to maintain buoyancy. This condition is associated with the swim bladder, a gas-filled organ that aids fish in remaining buoyant at varying water depths. The symptoms of swim bladder disease are quite distinctive and include difficulty in maintaining buoyancy which causes the fish to either float to the top or sink to the bottom, abnormal swimming patterns such as swimming on the side or upside down, and a bloated appearance or a visibly enlarged belly.

    Several factors can contribute to the onset of swim bladder disease. Overfeeding is a common cause, leading to constipation which may press against the swim bladder. Bacterial or viral infections affecting the swim bladder can also trigger this condition.[76] Physical injury or congenital deformities of the swim bladder are other potential causes.

  • Clownfish 

    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 symbiotic mutualisms 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 17 cm (6+12 in), while the smallest barely achieve 7–8 cm (2+34–3+14 in).

    Distribution and habitat

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    Anemonefish are endemic to the warmer waters of the Indian Ocean, including the Red Sea, and Pacific Ocean, the Great Barrier ReefHawaii, 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]

    Diet

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    Ocellaris clownfish nestled in a magnificent sea anemone (Heteractis magnifica)

    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

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    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]

    Anemonefish are the best known example of fish that are able to live among the venomous sea anemone tentacles, but several others occur, including juvenile threespot dascyllus, certain cardinalfish (such as Banggai cardinalfish), incognito (or anemone) goby, and juvenile painted greenling.[13][14][15]

    Reproduction

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    Clownfish swimming movements

    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]

    Parental investment

    [edit]

    A pair of pink anemonefish (Amphiprion perideraion) in their anemone home

    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]Duration: 38 seconds.0:38Video of a cinnamon clownfish swimming around an anemone

    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

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    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 complexesperculatomatoskunkclarkiisaddleback, 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 . allardi A. bicinctusA. chagosensisA. chrosgasterA. fuscocaudatusA. 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]

    Species

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    Scientific nameCommon nameClade[24]ComplexImage
    Genus Amphiprion:[28]
    A. akallopisosSkunk anemonefishA. akallopisosSkunk
    A. akindynosBarrier Reef anemonefishAustralianA. clarkii
    A. allardiAllard’s anemonefishIndianA. clarkii
    A. barberiBarber’s anemonefishA. ephippiumA. ephippium
    A. bicinctusTwo-band anemonefishIndianA. clarkii
    A. chagosensisChagos anemonefishIndianA. clarkii
    A. chrysogasterMauritian anemonefishIndianA. clarkii
    A. chrysopterusOrange-fin anemonefishMonospecific lineageA. clarkii
    A. clarkiiClark’s anemonefishA. clarkiiA. clarkii
    A. ephippiumRed saddleback anemonefishA. ephippiumA. ephippium
    A. frenatusTomato anemonefishA. ephippiumA. ephippium
    A. fuscocaudatusSeychelles anemonefishIndian[n 1]A. clarkii
    A. latezonatusWide-band anemonefishMonospecific lineageSaddleback
    A. latifasciatusMadagascar anemonefishIndianA. clarkii
    A. leucokranosWhite-bonnet anemonefishLikely hybridSkunk
    A. mccullochiWhitesnout anemonefishAustralianA. ephippium
    A. melanopusRed and black anemonefishA. ephippiumA. ephippium
    A. nigripesMaldive anemonefishIndianSkunk
    A. ocellarisOcellaris anemonefishA. perculaClownfish
    A. omanensisOman anemonefishIndianA. clarkii
    A. pacificusPacific anemonefishA. akallopisosSkunk
    A. perculaPercula anemonefishA. perculaClownfish
    A. perideraionPink skunk anemonefishA. akallopisosSkunk
    A. polymnusSaddleback anemonefishA. polymnusSaddleback
    A. rubrocinctusAustralian anemonefishA. ephippiumA. ephippium
    A. sandaracinosOrange anemonefishA. akallopisosSkunk
    A. sebaeSebae anemonefishA. polymnusSaddleback
    A. thielleiThielle’s anemonefishLikely hybridSkunk
    A. tricinctusThree-band anemonefishA. clarkiiA. clarkii
    Genus Premnas:[29]
    P. biaculeatusMaroon anemonefishPerculaMaroon

    Morphological diversity by complex

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    In the aquarium

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    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]

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    Finding Nemo birthday cakes featuring clownfish are popular.

    In Disney Pixar‘s 2003 film Finding Nemo and its 2016 sequel Finding Dory main characters Marlin, his son Nemo, and his wife 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]