Apistogramma hippolytae

Kullander, 1982

IUCNLEAST CONCERN · 2018
CARESNOT LISTED
Scientific size2 in5 cm standard length
Temperature73–86 °F23–30 °C
pH4.9–7neutral
Hardness (GH)slightly hardup to 179 ppm
Depth0–2 ft0–0.5 m
DietBenthic micro-invertivore (leaf-litter)
BreedingCave spawner, female-tended (facultative harem)~200 adhesive eggs
Sexual dimorphismYesSexes differ in colour more than size: males are the showier sex (blue wash low on the body, red-edged dorsal spines), while brooding females turn an intense yellow with blackened leading pelvic and dorsal rays. FishBase's length figures (males ~3.4 cm SL, females ~5.0 cm SL) suggest females are not smaller and may grow larger.
PhotographsSee photosGoogle Images →
For the aquarist

Replicate this biotopei

Target water

Temperature73.4–86.0 °F
pH4.9–7near neutral
Hardnessslightly hardup to 179 ppm

Recommended tank

Standard aquarium20-gallon “long”30 × 12 × 13 in · 20 gal (76 L)

Aquascape & setup

Soft to moderately soft water on the acidic side of neutral, in keeping with its lowland-river home — consistency counts for more than precision.

Driftwood, roots and leaf litter over a soft substrate echo a wooded river margin. Moderate, steady flow and shaded light suit a fish from slower backwaters; plants and wood double as cover.

Biotope tankmates

Other fish recorded from The Amazon Basin, of broadly compatible size — a starting shortlist, not a stocking plan. Always check temperament and territory before mixing.

Hybridization watchi

Apistogramma hippolytae is a small, plainly dressed dwarf cichlid of the central Brazilian Amazon, named half in jest for Hippolyta, the mythical queen of the Amazons. Its real distinction is not colour but the speed at which it changes colour: a field study off the Rio Negro recorded wild fish flicking between roughly half a dozen distinct patterns in seconds, using their skin as a quick, low-cost broadcast of mood, rank and readiness to spawn. It lives among shaded leaf litter in shallow, soft, acidic forest waters. Modestly popular in the hobby, it is one of the easier Apistogramma to breed — provided a keeper gives it the soft, acidic water it comes from.

What's in the name

Apistogramma hippolytaeap-iss-toh-GRAM-uh hip-POL-ih-tee

Descriptive name-eA third-declension descriptive adjective (“-e”, neuter).
Apistogramma
  • apistoGreekuncertain, inconstant — for the variable, often incomplete lateral line that puzzled early workers
  • grammaGreekline or graphic mark
hippolytae
  • hippolytaeotherof Hippolyta, queen of the Amazons in Greek myth — a play on the fish's occurrence in the Amazon basin; Kullander and FishBase both note the name carries no deeper significance for the species itself

Name history

  1. 1982Described by Kullander.
  2. Valid today as Apistogramma hippolytae Kullander, 1982.

Taxonomy & naming

Apistogramma hippolytae was described in 1982 by the Swedish ichthyologist Sven O. Kullander, in the German aquarium-science journal DCG-Informationen (bulletin of the Deutsche Cichliden-Gesellschaft), volume 13, number 10, page 182. The type locality is an igarapé — the Amazonian word for a small forest stream — feeding Lago Manacapuru in the Rio Solimões system of Amazonas state, Brazil. The holotype (MZUSP 6657) is held at the Museu de Zoologia da Universidade de São Paulo, with paratypes split between MZUSP and the Swedish Museum of Natural History in Stockholm (NRM 16672). Eschmeyer's Catalog of Fishes treats the name as valid and unchallenged, with no junior synonyms.

The genus name joins the Greek apisto, "uncertain," to gramma, "line" or "mark" — a nod to the variable, often incomplete lateral line that made these dwarf cichlids so hard to pin down. The epithet honours Hippolyta, queen of the Amazons in Greek myth; the link is to the Amazon basin rather than to any trait of the fish, and both Kullander and FishBase say plainly that it carries no deeper meaning. Placement differs between databases in the usual way — the Catalog of Fishes files the genus in subfamily Cichlinae, while FishBase keeps the older Geophaginae for the South American eartheaters and their dwarf relatives. Within the genus, the hobby's working scheme (Mike Wise and collaborators on apistogramma.com, building on Koslowski and Römer) places Apistogramma hippolytae in the broad regani-lineage rather than the more aggressively polygamous trifasciata-lineage that holds aquarium staples such as Apistogramma cacatuoides and Apistogramma agassizii.

Morphology

This is a genuinely small fish, even by dwarf-cichlid standards. FishBase gives a maximum of about 1.5 in standard length for males and roughly 2 in for females, with an older record of around 2.5 in total length; the IUCN account, following Kullander, cites about 1.5 in. Wild fish observed off the Rio Negro ran 1.5–3 in total length. At rest it sits at the plainer end of the genus — a base of golden-amber to silver-grey rather than the electric blues and reds of the show species.

The interest is that its appearance is not fixed. A field study of a wild population catalogued a silver-grey "plain" phase worn at rest and while feeding; a paler "stripe-spot" phase — lateral stripe, flank blotch and caudal spot — shown when the fish was disturbed or submissive; a "painted-face" phase with a single bold suborbital bar, flashed by large individuals about to attack; and high-contrast "barred" and "shining" phases used in aggression and courtship. Males in breeding condition add a wash of blue low on the body and red edging along the dorsal spines. The clearest signal comes from brooding females, which turn an intense yellow with the leading rays of the pelvic and dorsal fins blackened — the classic Apistogramma mother's livery, and the surest way to sex a spawning fish. Size is little help: FishBase's figures put females (to about 2 in SL) at or above the male maximum (about 1.5 in SL), so colour does the work, with males the more strongly marked sex.

Habitat

Apistogramma hippolytae is endemic to the Brazilian Amazon. The Catalog of Fishes and the IUCN place its core range in the middle Rio Negro drainage and Lake Manacapuru, with FishBase pinning Negro records near the mouths of the Urubaxi and Daraã rivers; the IUCN assessment extends it to the Rio Catuá and Rio Tefé in Amazonas state and the Rio Branco in Roraima, all within the wider Amazon basin.

It is a shallow-water, leaf-litter specialist of clear and black waters — the tea-stained, humic, often strongly acidic streams of the region — not the silty white-water main channels. The best data come from the study pond used by Rodrigues and colleagues near the Dimona research station of the Biological Dynamics of Forest Fragments Project, about 50 mi north of Manaus in a Rio Negro tributary system. The pond was small and shaded by overhanging rainforest, its bottom carpeted in fine sediment, dead leaves, twigs and fallen trunks, and almost everywhere less than half a metre deep. Their in-situ readings are unusually complete for this fish: temperature held a steady 76–79 °F through the day, pH ran a very acidic 4.9–5.0, conductivity was extremely low at 8.6–8.8 µS, and dissolved oxygen was a modest 3.5–4.7 mg/L. Those figures sit at the soft, acidic end of FishBase's broader envelope — pH up to about 7.0, hardness up to roughly 10 dH, temperatures of 73–86 °F — and are a truer guide to where the species actually lives than the wider tolerances a database has to report.

Feeding

Like most Apistogramma, Apistogramma hippolytae is a small benthic micro-predator, working the leaf litter and soft sediment for invertebrates and other tiny prey; FishBase places it at a trophic level near 3.3 — a modest carnivore, not a top predator. No dedicated gut-content study has been published, so the diet is inferred from the genus and the habitat, where the usual fare is microcrustaceans, insect larvae, worms and other small benthos picked and sifted from the substrate.

Field observation fills in the daily routine. The fish gathered in loose aggregations along the shallow margins, typically in subgroups of four or five without tight coordination, the clustering driven mostly by patchy food. Large males over about 2.5 in were not territorial in the strict sense but would seize a temporary foraging patch and shove smaller fish out of it — brief, low-stakes butting rather than real combat. These little cichlids share the litter with larger predators, above all pike cichlids (Crenicichla), and that pressure is the simplest reason the cryptic "plain" pattern, which dissolves into pale leaf debris, is the one they wear most of the time.

Mating

Reproduction reorganizes the population around females. In the Rodrigues study, ripe females settled into small areas of the pond and courted, while males — holding larger, looser territories — chose among the females ready to spawn, accepting one only if she produced a clutch within a few days of settling. When several females tried to settle at once the largest settled first, and females were least aggressive toward the resident male during this window. The result is a facultative harem: a male holds several females where habitat and sex ratio allow, but the system rests on female site-settlement and male mate-choice rather than rigid male herding. That "harem" label needs the usual regani-lineage caveat — experienced keepers call these fish casually or facultatively polygamous, forming a harem when conditions allow but readily pairing off, rather than the obligate harem breeders of parts of the trifasciata-group.

The standout behaviour, documented in the same population, is rapid colour signalling. Across more than a thousand observations the fish matched roughly half a dozen patterns to seven behaviours — foraging, resting, sexual and agonistic display, attack, flight and parental care — switching most of them in well under a minute. A large male would flip to its bold "painted-face" mark, drive off a rival, and revert to plain grey in under twenty seconds. In clear, shallow water, the authors argued, this fast skin signalling is an efficient way to advertise mood and status and to avoid wasting energy on needless fights.

Breeding

Apistogramma hippolytae is a cave-spawning, female-tended dwarf cichlid — the genus-typical mode, confirmed for this species in the field and in aquaria. FishBase reports clutches of about 200 adhesive eggs tended by the female, with harem polygyny when females outnumber available males. In the wild, Rodrigues and colleagues found the eggs laid out of sight beneath dead leaves rather than in an excavated pit, and located spawning fish by the brooding female's intense yellow-and-black livery, which — unlike the fast display colours — came on gradually and lingered. The eggs were adhesive and U-shaped to oval. After hatching, the female led and guarded the cryptic fry, following them even once they left the nest and turning sharply on the male whenever he neared the young, so his role is effectively limited to outer defence.

That single-parent investment carries a measurable cost. The study set out to test reproductive trade-offs and found them: brooding females fed less often than non-breeding fish, spent disproportionate time chasing intruders, and discriminated among threats — moving as much as 23.5 in out toward an approaching pike cichlid (Crenicichla) while merely shooing off lesser intruders. The cycle is straightforward to reproduce in the aquarium: the female seals herself and the eggs into a cave (a half-coconut or small flowerpot serves), the male patrols outside, and after roughly a week she leads a cloud of free-swimming fry into the open before turning intolerant of the male. Its long track record of captive spawning — including entries in the Greater Chicago Cichlid Association's Breeders Award Program — is a good sign that ordinary hobbyists raise it to free-swimming fry with some regularity.

In the aquarium

Apistogramma hippolytae is imported only occasionally rather than kept as a staple, but it has a solid captive record — it appears on the Greater Chicago Cichlid Association's Breeders Award Program list, and breeding accounts circulate in North American and European clubs — so an attentive keeper can expect to raise it. Chemistry, not tank size, is the thing to get right.

Water: its wild streams are extreme (pH near 4.9–5.0, conductivity under 9 µS, oxygen on the low side). Many keepers spawn it at pH 5.5–6.5 in soft water — hardness well under 10 dH, conductivity ideally under 100 µS — while others push closer to the wild figures using RO water reconstituted with a blackwater extract or dried leaves. Kept long-term in harder, alkaline tap water it looks washed out, feeds poorly and rarely spawns; that is the commonest mistake with this fish.

Tank: 15–20 US gal (about a 60 × 15.5 in footprint) suits a pair, and 20–30 US gal gives room for a harem of one male with two or three females. Floor space beats height — this is a bottom-hugging fish of water barely half a metre deep in the wild. Fine, pale-to-buff sand is far better than coarse gravel, which traps waste and can fray the fins. A layer of dried leaves (Catappa/Indian almond, oak or beech) over part of the floor is functional, not decorative: it gives cover and releases tannins that soften and acidify the water. Dim lighting — a low LED, or the shade of floating plants such as Ceratopteris or Salvinia — keeps the fish settled.

Caves and tankmates: breeding needs caves, and they steady the fish even between spawns. Ceramic tubes, half-coconut shells or notched clay flowerpots all work, with an entrance snug enough that the male cannot follow the female inside; a dominant male will guard several caves and the female occupying each. Small surface-schooling dither fish help the cichlids feel safe in the open — a dozen or more cardinal or rummy-nose tetras are both chemically suited and natural Rio Negro neighbours, and Corydoras make fair bottom companions in a larger tank if the species chosen takes soft, acidic water. Avoid larger cichlids and any bottom-dweller likely to harass a brooding female. In a harem, give each female her own cave and break the sightlines between them with driftwood, stone or leaf piles, or the dominant female will drive the others out; a simple pair yields fewer fry but is easier and the sensible default in a modest tank.

Breeding: a drop of a degree or two, or a big soft-water change, usually triggers spawning. At 75–79 °F the roughly 200 adhesive eggs hatch in about three days and the fry swim free a few days later; the female then shepherds them for two to three weeks on newly hatched Artemia nauplii and micro-fry foods, and in a small tank the male is best moved out once she turns on him. Overall difficulty is moderate, driven almost entirely by water chemistry — a keeper already running soft, acid water for cardinal tetras will find this a short step.

Conservation

The IUCN Red List assesses Apistogramma hippolytae as Least Concern. The evaluation was carried out by Brazil's Instituto Chico Mendes de Conservação da Biodiversidade (ICMBio), last assessed on 7 November 2018 and published in 2022; the population trend is stable, the species is described as frequent and abundant, and no significant threats were identified. It is endemic to Brazil — ranging across the middle Rio Negro, Lake Manacapuru, the Catuá and Tefé rivers in Amazonas and the Rio Branco in Roraima — and occurs inside at least one protected area, the Catuá-Ipixuna Extractive Reserve. It is collected for the ornamental aquarium trade, nationally and internationally, under Brazilian regulation; that collection is the main human pressure on it and is not currently a population-level risk. FishBase's model scores — high resilience (population doubling time under fifteen months) and low fishing vulnerability — fit that picture.

The honest framing is that the species is in good shape while the basin around it is not uniformly so. As a wide-ranging, fecund little fish of clear and black waters, Apistogramma hippolytae lacks the narrow-endemic fragility of many Amazonian cichlids. But the standard reference for the fauna — Kullander's cichlid chapter in the Reis, Kullander and Ferraris Check List of the Freshwater Fishes of South and Central America (2003) — describes extraordinary diversity under real, broad pressure: catchment deforestation and land-use change, sedimentation, dams, and the steady growth of both food and ornamental fisheries. For this fish the most direct of those is ornamental collection, which for now is sustainable and even gives some local economic reason to keep blackwater forest intact. The accurate summary: Apistogramma hippolytae is a Least Concern fish in a basin under mounting strain — secure today, but only as secure as the forest waters it shares with hundreds of less-buffered relatives.

In a guide: Dwarf cichlids

Sources

  1. Eschmeyer's Catalog of Fishes — Apistogramma hippolytae (Kullander 1982; valid; type locality, holotype MZUSP 6657)
  2. FishBase — Apistogramma hippolytae summary (size, water, diet, breeding, trophic level)
  3. FishBase — Apistogramma hippolytae common names (no established English name)
  4. GBIF — Apistogramma hippolytae (occurrence backbone)
  5. IUCN Red List — Apistogramma hippolytae (ICMBio 2022; assessed 7 Nov 2018; Least Concern, trend stable)
  6. Rodrigues, Carvalho, Zuanon, Del-Claro & Carvalho (2012), Reproductive behavior of the Amazonian dwarf cichlid Apistogramma hippolytae Kullander, 1982: offsetting costs and benefits, Acta Ethologica 15(1):1-7
  7. Rodrigues, Carvalho, Zuanon & Del-Claro (2009), Color changing and behavioral context in the Amazonian dwarf cichlid Apistogramma hippolytae, Neotropical Ichthyology 7(4):641-646
  8. Oliveira, Soares-Filho & Sousa-Lima (2009), Fish fauna of small streams of the Catuá-Ipixuna Extractive Reserve, Amazonas, Check List 5(1):154-172 (cited in IUCN range)
  9. Kullander, S.O. (2003), Cichlidae, in Reis, Kullander & Ferraris (eds.), Check List of the Freshwater Fishes of South and Central America, EDIPUCRS
  10. Mike Wise et al. — Apistogramma species-groups / lineages classification (regani-lineage placement)
  11. Greater Chicago Cichlid Association — Breeders Award Program species list (A. hippolytae bred and reported)
  12. Potomac Valley Aquarium Society — Apistogramma hippolytae breeding account
  13. Tropical Fish Hobbyist — The Apistogramma Aquarium (genus care and breeding)
  14. DwarfCichlid.com — Breeding Apistogrammas: a complete guide
  15. Apistogramma.com forum — regani-lineage polygamy vs. obligate harems (community discussion)community
  16. Buntbarsche Bulletin 209 (American Cichlid Association) — Rio Negro collecting account listing A. hippolytae among Apistogramma netted in shallow blackwater (anecdotal)community

Last reviewed 2026-06-08.

How to cite

Aquarist Atlas (2026). Apistogramma hippolytae. Aquarist Atlas. https://www.aquaristatlas.com/species/apistogramma-hippolytae/

Where it has been recorded

74 georeferenced records (GBIF). Each point is a field observation or museum specimen — pan and zoom to explore where this species turns up. The coordinates come straight from GBIF and are often rounded or tied to the nearest town or river landing, so a dot can sit just beside the actual water rather than in it; the fish aren't on dry land.

Preserved specimen: 74
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