Geophagus camopiensis PELLEGRIN, 1903

Oiapoque Eartheater

Etymology

Geophagus: from the Greek geo, meaning ‘earth’, and phagos, meaning ‘ to eat’.

camopiensis: named for the Camopi River, type locality of this species.

Classification

Order: Perciformes Family: Cichlidae

Distribution

Known only from the Oyapock (aka Oiapoque) river basin which forms much of the border between Amapá state, Brazil and eastern French Guiana, plus the Approuage system in French Guiana.

Type locality is ‘Camopi River, Oyapock basin, French Guiana’.

These two drainages run more-or-less parallel to one another and studies have shown them to be zoogeographically distinct from other rivers in French Guiana, meaning many of the fish species inhabiting them are unique.

Habitat

More than 90% of French Guiana is covered by tropical rain forest.

There are well-defined annual weather patterns with year-round high temperatures and two distinct wet seasons; the first between December and February and the second from April to June.

During these periods flow rate and depth of rivers can vary enormously, even on a daily basis, and turbidity also increases.

In a study conducted on the Arataye River, the main tributary of the Approuage, this species was mostly collected from stretches of rapids with rocky substrate which were reduced to a series of pools during the dry season.

Other fishes observed at the same site were Auchenipterus nuchalis, Hypostomus gymnorhynchus and Moenkhausia cf. intermedia while at other localities in the river Bryconops affinis, Myleus ternetzi, M. rhomboidalis, Moenkhausia aff. barbouri, Curimata sp. and Serrasalmus sp. were collected.

G. camopiensis is also likely to inhabit more typical Geophagus biotopes of gently sloping marginal zones around shores or islands with substrates of sand, fine gravel and mud.

Depending on locality other habitat features can include submerged tree roots, branches and leaf litter.

Other species from the Oiapoque known in the aquarium trade include Corydoras oiapoquensis, C. solox, C. sp. ‘C134’, C. sp. ‘C139’, Pseudancistrus niger/L039, Guyanancistrus brevispinis/L041, Apistogramma gossei, Astronotus ocellatus, Cichla monoculus, Guianacara geayi, Pterophyllum scalare, Hyphessobrycon roseus, H. takasei and Gasteropelecus sternicla.

Maximum Standard Length

180 – 200 mm.

Aquarium SizeTop ↑

An aquarium with a base measuring 150 ∗ 45 cm or more is required to house a group long-term.

Maintenance

The most essential item of décor is a soft, sandy substrate so that the fish can browse naturally (see ‘Diet’).

Coarser materials such as gravel or small pebbles can inhibit feeding, damage gill filaments and even be ingested with the potential of internal damage or blockages.

Additional furnishings are as much a case of personal taste as anything else but the most favoured set-ups tend to feature relatively dim lighting plus some chunks of driftwood and scattered roots or branches.

Leaf litter is a typical feature of the natural environment but not really recommended in aquaria because the feeding behaviour of Geophagus spp. tends to cause an excess of partially-decomposed material in suspension which not only looks unsightly but can block filter and pump mechanisms.

One or two flattish, water-worn rocks can also be included to provide potential spawning sites if you wish.

Water quality is of the utmost importance since these cichlids are extremely susceptible to deteriorating water quality and swings in chemical parameters so should never be introduced to a biologically immature aquarium.

The best way to achieve the desired stability is to over-filter the tank using a combination of external canister filters and/or a sump system and perform minimum weekly water changes of 50-70%.

If the maintenance regime is insufficient health issues such as head and lateral line erosion or stunted growth can occur.

Mechanical filtration should also be tailored to trap small particles stirred up by the fish as sand can cause blockages and wearing issues with filter mechanisms if allowed to continually run through the system.

High flow rates should be avoided so position filter returns accordingly.

Water Conditions

Temperature: This species prefers warm conditions of 25 – 33 °C.

pH: 6.0 – 7.5

Hardness: 36 – 215 ppm

Diet

Geophagus spp. are benthophagous by nature, employing a method of feeding whereby mouthfuls of substrate are taken and sifted for edible items with the remaining material expelled via the gill openings and mouth.

For this reason they’re commonly termed ‘eartheaters’ and the provision of a suitable substrate is essential to their long-term well-being.

Once settled they readily rise into the water column when food is introduced but continue to browse normally at other times.

The stomach contents of wild specimens mostly comprise small aquatic and terrestrial invertebrates, plant material in the form of seeds, organic detritus and sediment.

Even as adults these cichlids seem unable to properly ingest larger food items meaning the diet should contain a variety of high quality, fine-grade prepared foods plus small live or frozen bloodworm, Tubifex, Artemia, mosquito larvae, etc.

At least some of the dried products should contain a high proportion of vegetable matter such as Spirulina or similar.

Home-made, gelatine-bound recipes containing a mixture of dried fish food, puréed shellfish, fresh fruit and vegetables, for example, are proven to work well and can be cut into bite-sized discs using the end of a sharp pipette or small knife.

Rather than a single large meal offer 3-4 smaller portions daily to allow natural browsing behaviour as this seems to result in the best growth rate and condition.

Behaviour and CompatibilityTop ↑

Not the most peaceful member of the genus but will not predate on fishes larger than a few mm in length.

Suitable tankmates are far too numerous to list but include most peaceful species enjoying similar environmental conditions.

Best avoided are aggressive or territorial substrate-dwelling species, or those requiring harder water.

Some aquarists keep Geophagus spp. alongside freshwater stingrays of the genus Potamotrygon which in many cases has proven successful but in some has resulted in them disappearing at night (!).

G. camopiensis is gregarious and tends to exist in loose aggregations unless spawning, with juveniles in particular displaying strong grouping instincts.

A group of 5-8 individuals should be the minimum purchase and these will form a noticeable dominance hierarchy.

When maintained in smaller numbers weaker specimens can become the target of excessive antagonism by dominant individuals or the group may fail to settle and behave nervously.

Sexual Dimorphism

Young individuals are impossible to sex accurately by external means, but mature males tend to be a little larger and have longer finnage than females, with dominant specimens often developing a nuchal hump.

The ovipositor of the female is also visible when spawning.

Reproduction

Substrate-spawning, larvophilous, biparental mouthbrooder that has been bred in aquaria.

There doesn’t appear to be any particular trigger for the spawning process with the main requirements being good diet and stringent maintenance regime involving relatively large weekly water changes.

Since accurate sexing is very difficult it’s best to begin with a group of young fish and allow pairs to form naturally.

A degree of patience is also required since it can be at least a year until they become sexually mature.

Courtship is relatively unobtrusive consisting of fin flaring, circling, gaping and head jerking displays, and when ready to spawn a pair will select a suitable site.

This is normally a piece of décor such as a flat rock or section of driftwood although it’s not unknown for the base of the aquarium to be used, and once chosen the area is cleaned and defended against intruders.

Spawning occurs in typical substrate–spawning style with the female laying one or more rows of eggs before the male moves in to fertilise them, the process being repeated numerous times over a period of several hours.

Post-spawning the female stays close to the eggs, tending and defending them against intruders while the male is responsible for defence of the surrounding territory.

After around 72 hours the eggs hatch and fry immediately taken into the mouth of the female although on some occasions both parents may be involved from the start.

Once the fry are free swimming brood care/defence is shared although this varies depending on the male with some individuals becoming involved earlier and others not at all.

Some females therefore continue to hold all the fry or may even be driven away by the male to care for them alone.

In other cases both parents hold fry simultaneously or exchange the entire brood between one another on a regular basis, with such transfers tending to take place in a sheltered location such as a depression in the substrate.

When not brooding the adults will normally feed, and may even take some small morsels while holding fry.

The fry become free swimming at 8-11 days of age and the parents begin to release them to feed, initially with caution but for increasingly longer periods.

If danger is sensed the fry are shepherded back into the adults’ mouths, with rapid movement of the ventral fins appearing to act as a signal.

As time elapses and the fry grow they may only return to their parents’ mouths at night while the size of the territory becomes correspondingly larger.

They’re easily-fed, accepting good quality powdered dry foods, Artemia nauplii, microworm, etc. as soon as the free-swimming stage is reached.

If maintaining the adults in a community situation it’s recommended to remove brooding females as the fry become easy prey for other fishes, including conspecifics, once released.

NotesTop ↑

This species is poorly known in the aquarium hobby but occasionally available via specialist breeders and retailers.

It’s a member of the putative G. surinamensis ‘group’ of closely-related species within the genus and can be identified by a combination of characters including: no dark preopercular marking; no vertical bars on the flanks; relatively large dark midlateral marking; caudal fin patterning consisting of light blotches.

It also possesses only 30-31 scales in the E1 row (the scales in the row immediately above that containing the lower lateral line) and usually 7 anal fin rays, features shared only with G. parnaibae which may indicate a close relationship between the two species (Staeck and Schindler, 2006).

The remaining group members all have higher numbers of scales in the E1 row and usually 8 anal-fin rays.

G. camopiensis can be distinguished from G. parnaibae by possession of a larger (vs. smaller) dark lateral marking, light spots (vs. horizontal bands) in the caudal-fin, usually XVI (vs. XVII) dorsal spines, usually 11 (vs. 10) dorsal-fin rays.

Representatives of the G. surinamensis assemblage are diagnosed by their relatively deep head and body shape, possession of a variably-sized dark spot on each flank and presence or absence of a small, dark preopercular marking.

There are currently thirteen described members but diversity is predicted to eventually prove much greater with a number of undescribed forms known some of which, such as G. sp. ‘orange head’ and G. sp. ‘Pindare’, are regularly available in the aquarium trade.

The described members of the group are G. abalios, G. altifrons, G. brachybranchus, G. brokopondo, G. camopiensis, G. dicrozoster, G. megasema, G. neambi, G. parnaibae, G. proximus, G. surinamensis, G. sveni and G. winemilleri.

Only five Geophagus species aren’t included, namely G. argyrostictus, G. gottwaldi, G. grammepareius, G. harreri and G. taeniopareius.

These are most easily separated on the basis that they all possess a complete infraorbital stripe but oddly have not had their own group name assigned, usually being referred to simply as ‘non-G. surinamensis group’ species.

Accurate identification of G. surinamensis group members has been problematic for a number of reasons, not least that prior to Kullander (1986) G. surinamensis itself was thought to range throughout the Orinoco, Amazon and Guianas river systems but is now considered endemic to the Rio Surinam and Ri0 Maroni (aka Marowijne) watersheds in eastern Suriname.

Several former ‘populations’ have thus been described as species in their own right since the turn of the century, meaning older literature can be somewhat unreliable.

Further, the majority of Geophagus species in the hobby are sold as G. surinamensis regardless of origin – a situation which continues to cause confusion and exacerbated by the fact that juveniles of most are virtually identical.

G. surinamensis is in fact almost never traded and very few privately-owned specimens exist.

The number of species awaiting description is unconfirmed but it seems feasible that certain rivers within the Río Orinoco, rio Amazonas, rio Tocantins and rio Parnaíba basinsm, plus coastal drainages of the Guianas, contain one or two endemic forms.

Of those known in the aquarium hobby some are traded as G. sp. aff. altifrons which can be misleading as they don’t always resemble that species.

More preferable is to label with locality data when available.

The genus Geophagus was rediagnosed by Kullander (1986) who restricted it to include only those species with paired caudal extensions to the swimbladder lined by 6-12 epihemal ‘ribs’ plus a greater number of caudal than abdominal vertebrae.

Some former species were moved into the resurrected genus Satanoperca while others, such as the ‘Geophagus‘ brasiliensis and ‘G.‘ steindachneri groups represent distinct groupings still in need of definitive classification.

Geophagus and a number of related genera are often included in the putative subfamily Geophaginae.

Kullander (1998) conducted a morphology-based phylogenetic study in which the neotropical Cichlidae was divided into six subfamilies of which the Geophaginae contained 16 genera divided among three ‘tribes’:

Acarichthyini – Acarichthys and Guianacara.
Crenicaratini – Biotoecus, Crenicara, Dicrossus and Mazarunia.
Geophagini – Geophagus, Mikrogeophagus, ‘Geophagus‘ brasiliensis group, ‘Geophagus‘ steindachneri group, Gymnogeophagus, Satanoperca, Biotodoma, Apistogramma, Apistogrammoides and Taeniacara.

Later molecular studies by Farias et al. (1999, 2000, 2001) resulted in the additions of Crenicichla and Teleocichla to the Geophaginae, a result supported by López-Fernández et al. (2005) who conducted the most detailed molecular analysis of the grouping to date including 16 of the 18 genera and 30 species.

However their conclusions regarding interrelationships between genera did vary somewhat from previous hypotheses and can be summarised by the following loosely-defined groups:

– a weakly-supported sister group relationship between Acarichthys and Guianacara.
– a well-supported ‘Satanoperca clade‘ comprising Satanoperca, Apistogramma, Apistogrammoides and Taeniacara.
– a ‘big clade‘ with Geophagus, Mikrogeophagus, ‘Geophagus‘ brasiliensis group, ‘Geophagus‘ steindachneri group, Gymnogeophagus, Biotodoma, Crenicara and Dicrossus.
– a ‘crenicarine clade‘ with Biotoecus and Crenicichla.

No representatives of Teleocichla or Mazarunia were included in the study but the former is well-established as sister to Crenicichla while the latter has grouped closely with Dicrossus and Crenicara in earlier works.

The other main conclusions of the paper are confirmation that Geophaginae is a monophyletic group exhibiting strong signs of having undergone rapid adaptive radiation.

References

1. Boujard, T., 1992 - Environmental Biology of Fishes 34(3): 235-246
   Space-time organization of riverine fish communities in French Guiana.
2. Farias, I. P., G. Ortí, I. Sampaio, H. Schneider and A. Meyer, 1999 - Journal of Molecular Evolution 48(6): 703-711
   Mitochondrial DNA phylogeny of the family Cichlidae: monophyly and fast molecular evolution of the Neotropical assemblage.
3. Farias, I.P., G. Ortí, I. Sampaio, H. Schneider and A. Meyer, 2001 - Journal of Molecular Evolution 53(2): 89-103
   The cytrochrome b gene as a phylogenetic marker: the limits of resolution for analyzing relationships among cichlid fishes.
4. Jégu, M. and P. Keith, 1999 - Life Sciences 322(12): 1133–1143
   Le bas Oyapock limite septentrionale ou simple étape dans la progression de la faune des poissons d’Amazonie occidentale.
5. Kullander, S. O., 1986 - Swedish Museum of Natural History, Stockholm: 1-431
   Cichlid fishes of the Amazon River drainage of Peru.
6. Kullander, S. O. and H. Nijssen, 1989 - E.J. Brill, Leiden, The Netherlands: i-xxxii + 1-256
   The Cichlids of Surinam.
7. Lucinda, P. H. F., C. A. S. de Lucena and N. C. Assis, 2010 - Zootaxa 2429: 29-42
   Two new species of cichlid fish genus Geophagus Heckel from the Rio Tocantins drainage (Perciformes: Cichlidae).
8. López-Fernández, H. and D. C. Taphorn, 2004 - Zootaxa 439: 1-27
   Geophagus abalios, G. dicrozoster and G. winemilleri (Perciformes: Cichlidae), three new species from Venezuela.
9. López-Fernández, H., R. L. Honeycutt, M. L. J. Stiassny and K. O. Winemiller, 2005 - Zoologica Scripta 34(6): 627-651
   Morphology, molecules, and character congruence in the phylogeny of South American geophagine cichlids (Perciformes, Labroidei).
10. Reis, R. E., S. O. Kullander and C. J. Ferraris, Jr. (eds), 2003 - EDIPUCRS, Porto Alegre: i-xi + 1-729
    Checklist of the Freshwater Fishes of South and Central America. CLOFFSCA.
11. Schindler, I. and W. Staeck, 2006 - Zoologische Abhandlungen (Dresden) 56: 91-97
    Geophagus gottwaldi sp. n. - a new species of cichlid fish (Teleostei: Perciformes: Cichlidae) from the drainage of the upper rà o Orinoco in Venezuela.
12. Staeck, W. and I. Schindler, 2006 - Zoologische Abhandlungen (Dresden) 55: 69-75
    Geophagus parnaibae sp. n. -- a new species of cichlid fish (Teleostei: Perciformes: Cichlidae) from the rio Parnaà ba basin, Brazil.