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Apistogramma is a genus of the subfamily Geophaginae, tribe Geophagini.
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Apistogramma nijsseni, NRM 18078, adult male, 32.6 mm SL,
just collected from the wild near Jenaro Herrera, about 15 km on
road Jenaro Herrera-Colonia Angamos. 1 September 1981 (SOK 043).
Photo © S.O. Kullander.
Apistogramma is a geophagine genus with an unmistakable anteroventral expansion on the first epibranchial, the so-called geophagine lobe. The genus is distinguished by characters in combination, including the reduced number of external first ceratobranchial gill rakers (commonly 1, occasionally absent, exceptionally as many as 5), presence of gill rakers on the lower pharyngeal tooth-plate, absence of microgill-rakers and epibranchial 4 tooth plates, a single supraneural, few vertebrae (usually 12+12), and reduced lateralis system (only 2 infraorbitals, between lachrymal and sphenotic; lateral line scales to a great extent not developing tubes). Having separate openings for the posterior anguloarticular and rostralmost preopercular lateralis foramina is apparently a unique character state for Apistogrammoides and Apistogramma. Preopercular and posttemporal serrations are common. Sexual dimorphism is generally marked: males grow larger than females and often present relatively larger fins, commonly featuring prolonged rays in the caudal fin, produced dorsal fin lappets, and filamentous extension of the first pelvic fin ray; females have species specific brooding colour pattern consisting of contrasting yellow ground colour and intense black or dark brown markings.
Within the genus there are further reductions of the lateralis canal system, to some extent helpful for identification purposes, including (1) loss of the anguloarticular canal; (2) loss of one infraorbital foramen; (3) loss of the next to posteriormost dentary lateralis foramen. The basic Apistogramma pattern is featured by the so called regani group species (A. regani, A. eunotus, A. moae, A. urteagai, A.cruzi, A. resticulosa, A. caetei, A. piauiensis, A. gossei, A. geisleri, A. ortmanni) and others. Type 1 reduction is found in, e.g., A. borellii. Type 2 reduction is found in cacatuoides group (A. cacatuoides, A. juruensis, A. luelingi) and nijsseni group (A. nijsseni, A. payaminonis, A. norberti) species and others. Combined Type 2 and Type 3 reduction is encountered in A. agassizii, A. bitaeniata, A. eremnopyge and a few other species.
Most species have three anal fin spines, but at least three species regularly (A. commbrae, A. hoignei) or nearly invariably (A. luelingi) have four anal-fin spines. The number of anal fin spines is the single important distinguishing character from the monotypic Apistogrammoides, which is unique among geophagines in having as many as 6-9 anal fin spines. Another similar genus is the monotypic Taeniacara from central Amazonia with more reduced lateralis system, lacking the second frontal lateralis foramen, one pterotic lateralis foramen and the anguloarticular lateralis canal, and having the infraorbital bones reduced to a single or two small bones without lateralis canal.
Colour pattern is the most useful tool for identifying Apistogramma species insofar as form and distribution of melanophore based markings are concerned. Character state analysis, however, has not kept pace with descriptions and homology analysis and terminology is not comparable. Various markings designated by the same term may be non-homologues (e.g., abdominal stripes) and some markings are certainly composites, the nature of which is masked by the use of yet another name (e.g., tail-spot, for the marking formed by the combined Bar 7 and the caudal spot).
Apistogramma species are popular aquarium fishes; several popular books, e.g., Koslowski (2002), give useful information on life colours and reproductive behaviour based on aquarium studies. The genus was first revised by Regan (1906) and again revised by Kullander (1980), with partial revisions in Kullander (1986, 1987). These small colourful fishes are unfortunately attractive also for amateurs wishing to publish names on new species.
FOWLER, H.W. 1954. Os peixes de agua doce do
Brasil. Volume II. Archos Zool. S. Paulo, 9: 1-400.
KOSLOWSKI, I. 2002. Die Buntbarsche Amerikas. Band 2: Apistogramma & Co.. Verlag Eugen Ulmer, Stuttgart, 318 pp.
KULLANDER, S.O. 1980. A taxonomical study of the genus
Apistogramma Regan, with a revision of Brazilian and
Peruvian species (Teleostei: Percoidei: Cichlidae). Bonner
Zoologische Monographien, 14: 1-152.
KULLANDER, S.O. 1986. Cichlid fishes of the Amazon River drainage
of Peru. Swedish Museum of Natural History, Stockholm, 431
pp.
KULLANDER, S.O. 1987. A new Apistogramma species from the
Rio Negro in Brazil and Venezuela. Zool. Scr., 16: 259-270.
MEINKEN, H. 1962. Eine neue Apistogramma-Art aus dem
mittleren Amazonas-Gebiet, zugleich mit dem Versuch einer
Übersicht über die Gattung. Senckenberg. biol., 43:
137-143.
REGAN, C.T. 1906. A revision of the South-American cichlid genera
Retroculus, Geophagus, Heterogramma, and
Biotoecus. Ann. Mag. nat. Hist. (7), 17: 49-66.
REGAN, C.T. 1913. Fishes from the River Ucayali, Peru, collected
by Mr. Mounsey. Ann. Mag. nat. Hist. (8), 12: 281-283.
RÖMER, U. 1997. Diagnoses of two new dwarf cichlids
(Teleostei: Perciformes) from Peru, Apistogramma atahualpa
and Apistogramma panduro n. spp. Buntbarsche Bulletin 182:
9-14.
Apistogramma
arua sp.n. (Teleostei: Perciformes: Cichlidae), a new species
of dwarf cichlid from the Rio Arapiuns system, Para State,
Brazil. Aqua, 3: 45-54. -->