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?Cichlids
Common freshwater angelfish, Pterophyllum scalare
Common freshwater angelfish,
Pterophyllum scalare
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Actinopterygii
Order: Perciformes
Family: Cichlidae
Subfamilies

Astronotinae
Cichlasomatinae
Cichlinae
Etroplinae
Geophaginae
Heterochromidinae
Paratilapiinae
Pseudocrenilabrinae
Ptychochrominae
Retroculinae
For genera, see below.

Cichlids (pronounced /ˈsɪklɪd/) are fishes from the family Cichlidae in the order Perciformes. The family Cichlidae, a major family of perciform fish, is both large and diverse. Estimates of the number of cichlid species range from 1,900 to 2,200, making it one of the three largest vertebrate families.[1][2] Cichlids span a wide range of body sizes, from species as small as 2.5 centimetres (1.0 in) in length (e.g. Neolamprologus multifasciatus ) to much larger species approaching 1 metre (3 ft) in length (e.g. Boulengerochromis and Cichla). As a group, cichlids exhibit a similarly wide diversity of body shapes, ranging from strongly laterally compressed species (such as Altolamprologus, Pterophyllum, and Symphysodon) through to species that are cylindrical and highly elongate (such as Julidochromis, Teleogramma, Teleocichla, Crenicichla, and Gobiocichla).[3] Generally, however, cichlids tend to be of medium size, ovate in shape and slightly laterally compressed, and generally very similar to the North American sunfishes in terms of morphology, behaviour, and ecology.[4]

Many cichlids, particularly the tilapias, are important food fishes, while others are valued game fish (eg. Cichla species). Many species, including the angelfish, oscars, and discus, are also highly valued in the aquarium trade.[3][5] Cichlids are also the family of vertebrates with the largest number of endangered species, most of these found in the haplochromine group.[6] Cichlids are particularly well known for having evolved rapidly into a large number of closely related but morphologically diverse species within large lakes, particularly Tanganyika, Victoria, Malawi, and Edward, .[7][8] The diversity of cichlids in the African Great Lakes is important for the study of speciation in evolution.[9] Many cichlids that have been accidentally or deliberately released into freshwaters outside of their natural range have become nuisance species, for example tilapia in the southern United States.[10]

Anatomy and appearance[]

File:Labroidei relationships.png

Relationships within the Labrodei.[11]

Cichlids are members of a group of perciform fish known as the Labroidei alongside the wrasses Labridae, damselfish Pomacentridae, and surfperches Embiotocidae.[11] This very large grouping shares a single key trait: the fusion of the lower pharyngeal bones into a single tooth-bearing structure. A complex set of muscles allows the upper and lower pharyngeal bones to be used as a second set of jaws for processing food, allowing a division of labour between the "true jaws" (mandibles) and the "pharyngeal jaws". Cichlids in particular have evolved to be very efficient feeders that are able to capture and process a very wide variety of food items and this is assumed to be one reason why they are so diverse (see section on diet below).[3] Cichlids have a great variability in body shape, ranging from compressed and disc-shaped (such as Symphysodon) to elongate and cylindrical (such as Crenicichla.[12]

The particular features of cichlids that distinguish them from the other Labroidei include:[1]

  • A single nostril on each side of the forehead instead of two.
  • No bony shelf below the orbit of the eye.
  • The lateral line organ is divided into two sections, one on the upper half of the flank and a second along the midline of the flank from about halfway along the body to the base of the tail (except for genera Teleogramma and Gobiocichla).
  • A distinctively shaped otolith.
  • The small intestine leaves the stomach from its left side, not from its right side as in other Labroidei.

Taxonomy[]

Kullander (1998) recognises eight subfamilies of cichlids: the Astronotinae, Cichlasomatinae, Cichlinae, Etroplinae, Geophaginae, Heterochromidinae, Pseudocrenilabrinae and Retroculinae.[2] Nelson (2006), however, indicates that cichlid taxonomy is still greatly debated, and despite these attempts, classification of genera cannot yet be accurately given.[12] A comprehensive system of assigning species to monophyletic genera is still lacking, and there is not complete agreement on what genera should be recognized in this family.[12]

As an example of the extant problems in Cichlid taxonomy, Kullander published a phylogeny of the Cichlidae (details of which can be found here) in which the African genus Heterochromis ended up being placed phylogenetically within Neotropical Cichlds, although later papers arrived at different conclusions. Other extant problems (mentioned in the following paragraph) centre upon the identity of the putative common ancestor for the Lake Victoria superflock, and the precise ancestral lineages of the Tanganyikan Cichlids. However, the research is active and intensive (see below for just two of many recent papers), with new papers expected in the immediate future that may resolve some of the outstanding questions.

The paper Multilocus Phylogeny of Cichlid Fishes (Pisces: Perciformes): Evolutionary Comparison of Microsatellite and Single-Copy Nuclear Loci by Streelman, Zardoya, Meyer and Karl (1998) (Mol. Biol. Evol. 15(7):798–808. 1998, paper available as PDF here) provides comparisons between the phylogeny (due to Stiassny, 1991) as determined using morphological characteristics, and two maximum-pasrimony bootstrap consensus trees based upon analyses of two different gene loci, along with majority-rule trees and other similar phylogenetic trees based upon assorted gene locus analyses. There are some extant differences between the assorted trees at the genus level that require resolution, though the consensus from the various nuclear and mitochondrial DNA analyses in this and other papers is that the Cichlidae as a family is monophyletic. Further insights into the attractiveness of Cichlid taxonomy as a fertile area of research is given by the paper The species flocks of East African cichlid fishes: recent advances in molecular phylogenetics and population genetics by Salzburger and Meyer (Naturwissenschaften (2004) 91:277–290, paper available as PDF here), in which the advances made in the analysis of the phylogeny of the Lake Victoria superflock (among other East African Cichlids) is discussed in depth.

One problem that resulted in a major upheaval of Cichlid taxonomy was highlighted by Dr Humphrey Greenwood of the Natural History Museum, London, in a paper in 1977 (cited in TFH magazine, August 1977, with a follow up letter by Dr Greenwood in the November 1977 issue complaining about poor reportage of his work). Dentition (characteristics of tooth shape and arrangement) had been used prior to this date as classifying characteristics, which Greenwood demonstrated was invalid upon phylogenetic grounds because in many Cichlid species, dentition is an environmentally plastic characteristic (tooth shape changes in numerous species with age, due to wear etc), and cannot be relied upon universally across the family as a diagnostic characteristic upon which to base phylogenetic judgements. It is in the light of this that Cichlid taxonomy has undergone major revisions in the 30-plus years since, with the advent of genome sequencing and other technologies adding to the ever-growing body of data resulting in the still-fluid state of Cichlid taxonomy at the genus level.

Range and habitat[]

File:Tilapia mariae Australia.jpg

Tilapia mariae, caught on a hook and line, in Australia. Originally from Africa, the species established feral populations in Australia.[13]

Cichlids are the most species-rich non-Ostariophysan family in freshwaters worldwide. They are mainly freshwater fish that are most diverse in Africa and South America. It is estimated that there will be at least 1600 species in Africa alone when all are discovered and described.[12] Substantial numbers are also found in Central America from Panama to the Mexican portion of North America, with approximately 120 species, as far north as the Rio Grande in southern Texas, and Madagascar has its own distinctive fauna of cichlids phylogenetically only distantly related to those on the African mainland.[1][14] Endemic cichlids are largely absent in Asia except for four species in the Jordan Valley in the Middle East, one in Iran, and three in India and Sri Lanka.[12] There are three species found in Cuba and Hispaniola. Europe, Australia, Antarctica, and North America north of the Rio Grande River drainage, do not have any native cichlids, although where environmental conditions are suitable, for example in Florida, Mexico (which also has several native species), Japan and northern Australia, feral populations of cichlids have become established as exotics.[15][13][16][17][18][19][20]

Cichlids are largely freshwater fish and are less commonly found in brackish and salt water habitats, though many species will tolerate brackish water for extended periods; Cichlasoma urophthalmus, for example, is equally at home in freshwater marshes and mangrove swamps, and can be found living and breeding in salt water environments such as the mangrove belts around barrier islands.[3] Several species of tilapias (species of Tilapia, Sarotherodon, and Oreochromis) are euryhaline and can disperse along some brackish coastlines between rivers.[12] Only a few cichlids, however, are found primarily in brackish or salt water, most notably Etroplus maculatus, Etroplus suratensis, and Sarotherodon melanotheron.[21]

Diet[]

File:Pseudotropheus Crabo Male .JPG

The bumblebee cichlid, Pseudotropheus crabro, is specialised in feeding on parasites from the catfish Bagrus meridionalis[22]

Cichlids are astonishingly diverse in terms of diet. Many are primarily herbivores feeding on algae (e.g. Petrochromis) and plants (e.g. Etroplus suratensis) and small animals, particularly invertebrates, are only a small part of their diet. Some cichlids are detritivores and eat all types of organic material; among these species are the tilapiines of the genera Oreochromis, Sarotherodon, and Tilapia.

Other cichlids are predatory and eat little if any plant matter. These include generalists that catch a variety of small animals including other fishes and insect larvae (e.g. Pterophyllum), as well as variety of specialists. Trematocranus is a specialised snail-eater, while Pungu maclareni feeds on sponges. A number of cichlids feed on other fish, either whole or in part. Crenicichla are stealth-predators that lunge at small fish that pass by their hiding places, while Rhamphochromis are open water pursuit predators that chase down their prey.[23] Paedophagous cichlids such as the Caprichromis species eat other species' eggs or young (in some cases ramming the heads of mouthbrooding species to force them to disgorge their young).[24][25][22][26] Among the more unusual feeding strategies are those of Corematodus spp., Docimodus evelynae, Plecodus, Perissodus and Genyochromis species, which feed on scales and fins of other fishes, a behaviour known as lepidophagy[27][28][29] along with the death mimicking behaviour of Nimbochromis and Parachromis species, which lay motionless, luring small fish to their side prior to ambush.[30][31]

Scientists believe it is this wide adaptability of feeding styles that has helped cichlids to inhabit such a wide range of habitats. It is largely the pharyngeal teeth (teeth in the throat) that allows the cichlids so many 'niche' feeding behaviours, i.e. the jaws may be used to hold or pick food, while the pharyngeal teeth are used to crush what was harvested.

Reproduction[]

File:Managuense with eggs.jpg

A substrate brooding female managuense cichlid, Parachromis managuense, guards a clutch of eggs in the aquarium.

Brood care[]

All species show some form of parental care for both eggs and larvae, often extended to free-swimming young until they are several weeks or months old. Species of this family have highly organized breeding activities.[12]

Parental care falls into one of four categories:[32]Substrate or open brooders, secretive cave brooders (also known as guarding speleophils[33]), and at least two types of mouthbrooding, ovophile mouthbrooding and larvophile mouthbrooding.[34]

Open or substrate brooding cichlids lay their eggs in the open on rocks, leaves or logs. Examples of open brooding cichlids include Pterophyllum, Symphysodon spp and Anomalochromis thomasi. In general, brooding biparental substrate brooding cichlids usually engage in differing roles with regard to protection and raising of the fry. Most commonly, the male parent patrols the pair's territory and repels intruders, while females more intensively tend the brood, fanning water over the eggs, removing infertile eggs and leading the school of fry while foraging. Despite this, both sexes are able to perform the full range of parenting behaviours.[34] Secretive cave spawning cichlids lay their eggs in caves, crevices, holes or discarded mollusc shells (see also: shell brooding cichlids), frequently attaching the eggs to the roof of the chamber. Examples include Pelvicachromis spp., Archocentrus spp and Apistogramma spp.[32] Communication between free-swimming fry and parents of both open and cave spawning cichlids has been observed for a number of cichlids in captivity and in the wild.[34] Frequently this communication is based on body movements, such as shaking and pelvic fin flicking.[34] In addition, parental substrate brooding cichlids assist in finding food resources for their fry. Parental behaviours such as leaf-turning, and fin-digging have been observed for a number of neotropical cichlid species.[34]

Communal parental care, where multiple monogamous pairs care for a mixed school of young have also been observed for a number of cichlid species including: Amphilophus citrinellus, Etroplus suratensis and Tilapia rendalli.[35][36][37]

File:Cyphotilapia frontosa mouthbrooding.jpg

A female Cyphotilapia frontosa mouthbrooding fry which can be seen looking out her mouth

Ovophile mouthbrooders incubate their eggs in their mouths as soon as they are laid, and frequently continue to brood free-swimming fry in their mouths for several weeks. Examples of ovophile mouthbrooding cichlids include many of the cichlids endemic to the Rift Valley lakes (Lake Malawi, Lake Tanganyika and Lake Victoria) in east Africa eg: Maylandia, Pseudotropheus and Tropheus along with some south american cichlids such as Geophagus steindachneri. Larvophile mouthbrooding species lay the eggs in the open, or in a cave and upon hatching take the larvae into the mouth. Examples include some variants of Geophagus altifrons, some Aequidens, Gymnogeophagus and Satanoperca species.[3][32] Regardless of whether eggs or larvae are subject to mouthbrooding, the vast majority of mouthbrooding cichlids are maternal mouthbrooders, that is the female mouthbroods the young. In the eretmodine cichlids (genera Spathodus, Eretmodus and Tanganicodus), some Sarotherodon species, Chromidotilapia guntheri and some Aequidens species, however, mouthbrooding is practiced by both the male and the female.[3][38][34] Paternal mouthbrooding, though rare, is also known to occur in the family eg. Sarotherodon melanotheron.[39] This method is common and appears to have evolved independently in several groups of African cichlids.[12]

Several cichlids, including discus (Symphysodon spp.), some Amphilophus species, Etroplus and Uaru species are noted to feed their young with a skin secretion from mucous glands.[3][32]

Mating system[]

Cichlids are either monogamous or polygamous in their mating system.[3] The mating system of any given cichlid species is not consistently associated with the type of brood care the species employs. For example, although most monogamous cichlids are not mouthbrooding cichlids, Chromidotilapia, Gymnogeophagus, Spathodus and Tanganicodus are all monogamous mouthbrooders. In contrast, numerous open or cave spawning cichlids are polygamous, examples include Apistogramma, Lamprologus, Nannacara and Pelvicachromis.[3][40]

File:Lamprologus ocellatus fry.jpg

Lamprologus ocellatus, a shell-dwelling cichlid, guarding fry

Endangered cichlids[]

According to the 2007 International Union for Conservation of Nature and Natural Resources red list 156 cichlid species are currently listed as vulnerable, 40 species are listed as endangered, while 69 species are listed as critically endangered. Six species, Haplochromis ishmaeli, Haplochromis lividus, Haplochromis perrieri, Paretroplus menarambo, Platytaeniodus degeni and Yssichromis sp. nov. 'argens' are extinct in the wild, while at least 39 species, most from the genus Haplochromis, have become extinct since the early 1990s.[41]

Lake Victoria[]

Because of the introduced Nile perch (Lates niloticus) and water hyacinth, deforestation causing siltation of water, and overfishing, many species of Lake Victoria cichlids have been wiped out or drastically reduced in the wild. By around 1980, fisheries of the lake yielded only 1 percent cichlids from all the catch, a drastic decline from 80 percent in the earlier years.[42]

File:Astatotilapia latifasciata.png

Haplochromis latifasciata is critically endangered in the wild[43]

As many as three hundred species or about two-thirds of the endemic cichlids, especially the ones that feed in the open bottom of the lake, became endangered or extinct. Some surviving cichlids, however, have adapted to the new threats by becoming smaller or hybridising with other species.[42] Thankfully, the myriad of satellite lakes surrounding Lake Victoria have not been affected, and harbor an array of similar species.

Cichlids as food and game fish[]

Although cichlids are mostly small and medium-sized fishes, a substantial number of species are notable as food and game fishes. With few thick rib bones and tasty flesh, artisan fishing of cichlids is not uncommon in Central America and South America, as well as areas surrounding the African rift lakes.[42] The most important food cichlids, however, are the tilapiines of North Africa. Fast growing, tolerant of stocking density, and highly adaptable, tilapiine species have been introduced and farmed extensively in many parts of Asia and are increasingly common in other parts of the world. Production of farmed tilapia, at about 1.5 million tons annually with an estimated value of US$1.8 billion,[44] is about equal to that of salmon and trout. Unlike carnivorous salmon and trout, however, tilapia are mostly omnivorous and can feed on algae or any plant-based food. This reduces the cost of tilapia farming greatly and makes tilapia the ideal "aquatic chickens" of the trade.[42]

In addition to being food fish, many large cichlids also make good game fish. The strong, hard-fighting peacock bass (Cichla species) of South America is one of the most popular sportfish. It was intentionally released in many waters around the world. In Florida, this fish generates millions of hours of fishing and anglers' spendings of more than US$8 million a year.[45] Other cichlids preferred by anglers include the oscar, Mayan cichlid (Cichlasoma urophthalmus), and jaguar guapote (Parachromis managuensis).[45]

Cichlids as aquarium fish[]

File:Discus fish.jpg

Although not particularly hardy, the discus, Symphysodon spp., has been popular among aquarium enthusiasts.

Since 1945, cichlids have become increasingly popular as aquarium fish[34][3][32][46][47][48][49] Cichlids are ideally suited as aquarium fish as many are small to medium-sized, easy to feed with a range of prepared fish foods, breed readily, and practice brood care, in captivity.[32]

The most commonly encountered species in retail aquariums is Pterophyllum scalare from the Amazon River basin in tropical South America, known in the trade as the "angelfish" . Other popular or readily available species of cichlids include the oscar (Astronotus ocellatus), convict cichlid (Archocentrus nigrofasciatus) and discus (Symphysodon spp.).[3]

Species of cichlid can be kept in aquariums with other fish, however, many cichlids are predatory towards smaller fish.[32] Conversely, some cichlids, such as Apistogramma or Julidochromis spp., can be timid in the aquarium. In such cases the use of dither fish is recommended.[3]

Hybrid cichlids and selective breeding[]

File:Red Texas.jpg

The "red Texas" cichlid is not a Texas cichlid (Herichthys cyanoguttatus) but an intergeneric hybrid of Herichthys and Amphilophus parents.

Some cichlids have been found to hybridise with closely related species quite readily, both in the wild and under artificial conditions.[50] This is not particularly unusual, having been observed among other groups of fishes, such as European cyprinids.[51] What is unusual is the extent to which cichlid hybrids have been put to commercial use, in particular as food fish and as aquarium fish.[5][52] The red strain of tilapia hybrid, for example, is often preferred in aquaculture as they have faster growth rates. Tilapia hybridisation is also used to produce all-male populations to control stock density and prohibit reproduction in ponds.[5]

The most ubiquitous aquarium hybrid is perhaps the blood parrot cichlid which is a cross of several species especially those from genus Amphilophus. With a beak-shaped mouth, an abnormal spine, and an occasionally missing caudal fin (known as the "love heart" parrot cichlid), the fish has caused controversy among aquarium enthusiasts. Some has called blood parrot cichlid "the Frankenstein monster of the fish world."[53] Another notable hybrid, the flowerhorn cichlid, was very popular in some parts of Asia from 2001 until late 2003 and is believed to bring good luck to its owner.[54] The popularity of the flowerhorn cichlid declined in 2004,[55] resulting in many flowerhorn cichlids being released into the rivers and canals of Malaysia and Singapore where they pose a threat to endemic animal communities.[56]

File:Long finned oscar.jpg

A leucistic long-finned form of A. ocellatus

Numerous cichlid species have also been the subject of selective breeding programmes to develop new ornamental strains for the aquarium trade. The most intensive selective breeding programs have involved angelfish and discus and many mutations that effect both colouration and finnage are known.[3][57][58] Many other cichlids have been selecively bred for albino, leucistic and xanthistic pigment mutations including oscars, convicts and Pelvicachromis pulcher.[3][32] Both dominant and recessively inherited pigment mutations have been observed for cichlids.[9] In convict cichlids, for example, a leucistic colouration is recessively inherited,[59] while in Oreochromis niloticus niloticus red colouration is caused by an dominantly inherited mutation.[60]

These efforts at selectively breeding may, however, have unintended consequences. For example, some selectively bred strains of Mikrogeophagus ramirezi have health and fertility problems.[61] Similarly, the inbreeding involved in selective breeding programmes can cause severe physical abnormalies such as the notched phenotype in angelfish.[62]

Genera[]

As of 2006, there were some 220 genera: [1]

  • Acarichthys Eigenmann 1912
  • Acaronia Myers 1940
  • Aequidens Eigenmann & Bray 1894
  • Allochromis Greenwood 1980
  • Alticorpus Stauffer & McKaye 1988
  • Altolamprologus Poll 1986
  • Amatitlania Schmitter-Soto, 2007
  • Amphilophus Agassiz, 1859
  • Anomalochromis Greenwood 1985
  • Apistogramma Regan 1913
  • Apistogrammoides Meinken 1965
  • Archocentrus Gill 1877
  • Aristochromis Trewavas, 1935
  • Astatoreochromis Pellegrin 1904
  • Astatotilapia Pellegrin 1904
  • Astronotus Swainson 1839
  • Aulonocara Regan 1922
  • Aulonocranus Regan 1920
  • Australoheros Rican & Kullander 2006
  • Baileychromis Poll 1986
  • Bathybates Boulenger 1898
  • Benitochromis Lamboj 2001
  • Benthochromis Poll 1986
  • Biotodoma Eigenmann & Kennedy 1903
  • Biotoecus Eigenmann & Kennedy 1903
  • Boulengerochromis Pellegrin 1904
  • Buccochromis Eccles & Trewavas 1989
  • Bujurquina Kullander 1986
  • Callochromis Regan 1920
  • Caprichromis Eccles & Trewavas 1989
  • Caquetaia Fowler 1945
  • Cardiopharynx Poll 1942
  • Chaetobranchopsis Steindachner, 1875
  • Chaetobranchus Heckel, 1840
  • Chalinochromis Poll 1974
  • Champsochromis Boulenger 1915
  • Cheilochromis Eccles & Trewavas 1989
  • Chetia Trewavas 1961
  • Chilochromis Boulenger 1902
  • Chilotilapia Boulenger 1908
  • Chromidotilapia Boulenger 1898
  • Cichla Bloch & Schneider 1801
  • Cichlasoma Swainson 1839
  • Cleithracara Kullander & Nijssen 1989
  • Congochromis Stiassny & Schliewen 2007
  • Copadichromis Eccles & Trewavas 1989
  • Corematodus Boulenger 1897
  • Crenicara Steindachner 1875
  • Crenicichla Heckel 1840
  • Ctenochromis Pfeffer 1893
  • Ctenopharynx Eccles & Trewavas 1989
  • Cunningtonia Boulenger 1906
  • Cyathochromis Trewavas 1935
  • Cyathopharynx Regan 1920
  • Cyclopharynx Poll 1948
  • Cynotilapia Regan 1922
  • Cyphotilapia Regan 1920
  • Cyprichromis Scheuermann 1977
  • Cyrtocara Boulenger 1902
  • Danakilia Thys van den Audenaerde 1969
  • Dicrossus Steindachner 1875
  • Dimidiochromis Eccles & Trewavas 1989
  • Diplotaxodon Trewavas 1935
  • Divandu Lamboj & Snoeks 2000
  • Docimodus Boulenger 1897
  • Eclectochromis Eccles & Trewavas 1989
  • Ectodus Boulenger 1898
  • Enterochromis Greenwood 1980
  • Eretmodus Boulenger 1898
  • Etia Schliewen & Stiassny 2003
  • Etroplus Cuvier 1830
  • Exochochromis Eccles & Trewavas 1989
  • Fossorochromis Eccles & Trewavas 1989
  • Gaurochromis Greenwood 1980
  • Genyochromis Trewavas 1935
  • Geophagus Heckel 1840
  • Gephyrochromis Boulenger 1901
  • Gnathochromis Poll 1981
  • Gobiocichla Kanazawa 1951
  • Grammatotria Boulenger 1899
  • Greenwoodochromis Poll 1983
  • Guianacara Kullander & Nijssen 1989
  • Gymnogeophagus Miranda Ribeiro 1918
  • Haplochromis Hilgendorf 1888
  • Haplotaxodon Boulenger 1906
  • Harpagochromis Greenwood 1980
  • Hemibates Regan 1920
  • Hemichromis Peters 1857
  • Hemitaeniochromis Eccles & Trewavas 1989
  • Hemitilapia Boulenger 1902
  • Herichthys Baird & Girard 1854
  • Heros Heckel, 1840
  • Herotilapia Pellegrin 1904
  • Heterochromis Regan 1922
  • Hoplarchus Kaup,1860
  • Hoplotilapia Hilgendorf 1888
  • Hypselecara Kullander 1986
  • Hypsophrys Agassiz 1859
  • Interochromis Yamaoka, Hori & Kuwamura 1988
  • Iodotropheus Oliver & Loiselle 1972
  • Iranocichla Coad 1982
  • Ivanacara Romer & Hahn 2006
  • Julidochromis Boulenger 1898
  • Katria Stiassny & Sparks 2006
  • Konia Trewavas 1972
  • Krobia Kullander & Nijssen 1989
  • Labeotropheus Ahl 1926
  • Labidochromis Trewavas 1935
  • Labrochromis Greenwood 1980
  • Laetacara Kullander 1986
  • Lamprologus Schilthuis 1891
  • Lepidiolamprologus Pellegrin 1904
  • Lestradea Poll 1943
  • Lethrinops Regan 1922
  • Lichnochromis Trewavas 1935
  • Limbochromis Greenwood 1987
  • Limnochromis Regan 1920
  • Limnotilapia Regan 1920
  • Lipochromis Greenwood 1980
  • Lithochromis Lippitsch & Seehausen 1998
  • Lobochilotes Boulenger 1915
  • Macropleurodus Regan 1922
  • Maylandia Meyer & Foerster 1984
    • (see also Metriaclima)
  • Mazarunia Kullander 1990
  • Mbipia Lippitsch & Seehausen 1998
  • Mchenga Stauffer & Konings, 2006
  • Melanochromis Trewavas, 1935
  • Mesonauta Günther, 1862
  • Microchromis Johnson 1975
  • Mikrogeophagus Meulengracht-Madson 1968
  • Myaka Trewavas 1972
  • Mylacochromis Greenwood 1980
  • Mylochromis Regan 1920
  • Naevochromis Eccles & Trewavas 1989
  • Nandopsis Gill, 1862
  • Nannacara Regan]] 1905
  • Nanochromis Pellegrin 1904
  • Neetroplus Günther, 1867
  • Neochromis Regan 1920
  • Neolamprologus Colombe & Allgayer 1985
  • Nimbochromis Eccles & Trewavas 1989
  • Nyassachromis Eccles & Trewavas 1989
  • Ophthalmotilapia Pellegrin 1904
  • Oreochromis Günther 1889
  • Orthochromis Greenwood 1954
  • Otopharynx Regan 1920
  • Oxylapia Kiener & Maugé 1966
  • Pallidochromis Turner 1994
  • Parachromis Agassiz 1859
  • Paracyprichromis Poll 1986
  • Paralabidochromis Greenwood 1956
  • Parananochromis Greenwood 1987
  • Paraneetroplus Regan 1905
  • Paratilapia Bleeker, 1868
  • Paretroplus Bleeker, 1868
  • Pelmatochromis Steindachner 1894
  • Pelvicachromis Thys van den Audenaerde 1968
  • Perissodus Boulenger 1898
  • Petenia Günther, 1862
  • Petrochromis Boulenger 1898
  • Petrotilapia Trewavas 1935
  • Pharyngochromis Greenwood 1979
  • Placidochromis Eccles & Trewavas 1989
  • Platytaeniodus Boulenger 1906
  • Plecodus Boulenger 1898
  • Prognathochromis Greenwood 1980
  • Protomelas Eccles & Trewavas 1989
  • Psammochromis Greenwood 1980
  • Pseudocrenilabrus Fowler 1934
  • Pseudosimochromis Nelissen 1977
  • Pseudotropheus Regan 1922
  • Pterochromis Trewavas 1973
  • Pterophyllum Heckel 1840
  • Ptychochromis Steindachner 1880
  • Ptychochromoides Kiener & Mauge 1966
  • Ptyochromis Greenwood 1980
  • Pundamilia Seehausen & Lippitsch 1998
  • Pungu Trewavas 1972
  • Pyxichromis Greenwood 1980
  • Reganochromis Whitley 1929
  • Retroculus Eigenmann & Bray 1894
  • Rhamphochromis Regan 1922
  • Rocio Schmitter-Soto, 2007
  • Sargochromis Regan 1920
  • Sarotherodon Rppell 1852
  • Satanoperca Günther, 1862
  • Schubotzia Boulenger 1914
  • Schwetzochromis Poll 1948
  • Sciaenochromis Eccles & Trewavas 1989
  • Serranochromis Regan 1920
  • Simochromis Boulenger 1898
  • Spathodus Boulenger 1900
  • Steatocranus Boulenger 1899
  • Stigmatochromis Eccles & Trewavas 1989
  • Stomatepia Trewavas 1962
  • Symphysodon Heckel 1840
  • Taeniacara Myers 1935
  • Taeniochromis Eccles & Trewavas 1989
  • Taeniolethrinops Eccles & Trewavas 1989
  • Tahuantinsuyoa Kullander 1991
  • Tangachromis Poll 1981
  • Tanganicodus Poll 1950
  • Teleocichla Kullander 1988
  • Teleogramma Boulenger 1899
  • Telmatochromis Boulenger 1898
  • Theraps Günther, 1862
  • Thoracochromis Greenwood 1979
  • Thorichthys Meek 1904
  • Thysochromis Daget 1988
  • Tilapia Smith, 1840 See also: Tilapiine cichlids
  • Tomocichla Regan 1908
  • Tramitichromis Eccles & Trewavas 1989
  • Trematocara Boulenger 1899
  • Trematocranus Trewavas 1935
  • Triglachromis Poll & Thys van den Audenaerde 1974
  • Tristramella Trewavas 1942
  • Tridontochromis Greenwood 1980
  • Tropheops Trewavas 1984
  • Tropheus Boulenger 1898
  • Tylochromis Regan 1920
  • Tyrannochromis Eccles & Trewavas 1989
  • Uaru Heckel 1840
  • Variabilichromis Colombe & Allgayer 1985
  • Vieja Fernandez-Yepez 1969
  • Xenochromis Boulenger 1899
  • Xenotilapia Boulenger 1899
  • Xystichromis Greenwood 1980
  • Yissochromis Greenwood 1980

Images of cichlids[]

Main gallery: Cichlid images

See also[]

  • Perciformes
  • Aquaculture
  • Fishkeeping
  • Aquarium

References[]

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  3. 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 3.11 3.12 3.13 Loiselle, P.V. (1994). The Cichlid Aquarium, Tetra Press.
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Further reading[]

National Museum of Natural History, Washington, D.C., 2004-05-11).

External links[]

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