Brown Hoplo

Hoplosternum littorale

Callichthyidae · freshwater water fish

9 minute read · Species guide

Brown Hoplo field guide illustration

About Brown Hoplo

Hoplosternum littorale is a species of freshwater ray-finned fish belonging to the subfamily Callichthyinae of the family Callichthyidae, the armoured catfishes. It is known as Tamatá in Brazil, atipa in French Guiana, hassa in Guyana, kwi kwi (or kwie kwie) in Suriname, cascadu or cascadura in Trinidad and Tobago, and busco or currito in Venezuela.

Description

H. littorale is armor-plated and dorso-ventrally compressed. The fish will grow in length up to 24.0 centimetres (9.4 in) TL.

Males grow to a larger average and maximum size than females and, during the reproductive season, develop fat deposits in the pectoral fin and an elongated recurved pectoral spine that often assumes a reddish colour. Males with recurved pectoral spines are not found outside of the reproductive period.

Distribution

H. littorale has the widest distribution of any callichthyid. It is present in all of South America east of the Andes and north of Buenos Aires, including the Orinoco, Trinidad, coastal rivers of the Guianas, Amazon River drainage, Paraguay, lower Paraná River, and coastal systems in southern Brazil. It ranges from Venezuela and Guyanas to Argentina.

One single lot is known from the upper Paraná River and the São Francisco River drainage; it has been suggested that these occurrences may represent introduced populations. This species has also been introduced into the Indian River Lagoon of Florida.

Ecology

Most activity of non-breeding H. littorale such as feeding and locomotor activity are mainly nocturnal. It has a maximum reported age of 4 years. The diet of H. littorale consists mainly of benthic invertebrates and detritus.

H. littorale natively inhabits tropical standing waters or swamps. It is not found in rainforest creeks and clearwater rivers draining Precambrian Guyana and Brazilian Shields, where water is extremely poor in dissolved minerals. This species is restricted to swamps of tropical and subtropical South America and the floodplains of Amazonian whitewater rivers originating in the Andes. Such environments are characterized by low levels of dissolved oxygen and markedly seasonal conditions caused primarily by fluctuations in rainfall.

H. littorale can breathe both with gills and through its intestines. However, intestinal respiration is not exhibited upon hatching, and the development of the respiratory intestine occurs throughout the juvenile period (up to 32 days old). Newly hatched larvae do not have the ability to breathe air through their intestines; however, it is possible that they absorb oxygen through their skin at this point, before the armor plates have developed. Soon after, between about 12 – 23 days of age, young have the capacity to breathe air, but their respiratory intestine has not finished developing. The respiratory intestine is well-developed between days 24 and 32.

H. littorale has two types of hemoglobin, anodic and cathodic; anodic hemoglobin has a relatively low oxygen affinity and has marked Bohr effects, while cathodic hemoglobin lack significant pH effects. In H. littorale, cathodic hemoglobin has a pronounced reversed Bohr effect in which oxygen affinity increases with decreased pH. Cathodic hemoglobin has the purpose of safeguarding oxygen transport to tissues under hypoxic and acidotic conditions.

H. littorale diet varies by age. Immature fish feed primarily on small aquatic crustaceans, especially Cladocera, Ostracoda, Copepoda, and Eubranchipoda. Chironomid larvae are important items in the diets of both juveniles and adults. The adult diet is dominated by mixed detritus, terrestrial insects, microcrustaceans, and aquatic beetles during the dry season, and mixed detritus and chironomid larvae during the wet season.

Reproduction

The first reproduction occurs after one year. Spawning is triggered by the first rains and occurs in the warm and rainy season. As a callichthyine, it builds a bubble nest; among callichthyines, this species is reported to have the most complex nest structure. This dome-shaped nest is rich with oxygen; in the hypoxic water conditions of tropical swamps, the main function of the bubble nest appears to be to provide oxygen to the developing eggs by lifting the eggs above the water surface while protecting them from desiccation. It may also serve to protect the brood against predators, regulate temperature, identify the center of the male's territory, and to synchronize reproductive activities. Nest-building activities usually lasted from 1,000 to 1,500 hours, but only on clear and warm days, particularly during the hottest hours. These activities are also reported to occur at night. Most nests are built in newly flooded swamps, especially in open water in the peripheral area of the swamp. A minimum distance of 10 metres between nests is observed. The nest is the centre of a territory that is vigorously defended by the male, using its enlarged pectoral spines. The diameter and height of the nest average 30 and 6 cm (12 and 2.36 in), respectively.

The beginning of nest building is preceded by a courtship ritual. This pair formation consists of the male and female swimming parallel to each other, the male and female facing each other and contacting their barbels, the male stimulating the flanks of the female, the swimming to the surface by the male and female and production of the first bubbles at the nest site, and adding further bubbles to the nest under construction. The male produces most of the foam. First, the male and female come to the surface and swim belly-up in small circles. The film of the air-water interface is swallowed and pumped out through the gills, where it gains mucus. Movement of the pelvic fins stirs the water and mucus, captures air bubbles, and breaks these air bubbles into a foam. The female may add some bubbles to the nest under construction. Pelvic fin movement differs between sexes; males move their pelvic fins in a side-to-side fashion, while females open and close their pelvic fins. The male often dives to the bottom to retrieve plant debris; filamentous nest materials are preferred, which are knitted together in the nest by the male. The male creates an upward water current with its tail fin that lift plant materials up. Then, the male uses its developed pectoral fin spines to cary the plant materials to the nest. The male uses its mouth and pectoral fins to incorporate the plant material into the foam mass of the nest. Females neither have developed pectoral fin spines nor do they help in transporting plant debris. The result is a dome-shaped nest made up of loosely interwoven plant material on top of tightly interwoven plant material, held up to the surface with a layer of foam; the eggs will be laid on top of this foam from below.

Spawning occurs during the daytime. There is indication that the female drinks the sperm and that fertilization takes place after the sperm has passed through her digestive tract. The male and female form the "T-position", where the female places its mouth over the male's genital opening and collects the sperm in the mouth. The female rests at the bottom for 30 – 60 seconds, and then swims to the nest, turns upside down, and lays the eggs in the nest. H. littorale is a multiple spawner. Investing in reproduction is high in females since they can spawn up to 14 times during a 7-month breeding season and each spawn consists of 6,000 – 9,000 eggs. On average, two to four females spawn simultaneously, resulting in an average number of 20,000 eggs per nest. The adhesive eggs are located in the centre of the nest under the plant debris above the surface of the water, and not in contact with the oxygen-depleted swamp water. The male guards the nest during incubation; incubation of the eggs takes two to three days depending on the temperature in the nest. The male also regularly supplies foam to the nest. Guarding and maintenance of the nest occurs day and night. Once spawning has been completed, the male attacks females that have deposited their eggs in the nest. Despite intense predation pressure on eggs and larvae, the male's guarding behavior extends for only one or two days after hatching. The male attacks with its large pectoral spines erect; the attack consists of rapid propulsion towards its target followed by a sharp lateral turn, which causes the rough outer edge of pectoral spine to drag across the target and cause abrasion.

Relationship to humans

H. littorale is a valuable resource extensively fished in the deltas of the Amazon and Orinoco. In Guyana, French Guiana, Suriname, and Trinidad, this species is an extremely popular food fish.

H. littorale is commercially cultured in Trinidad, Guyana and Suriname. It fetched a price of US$8/kg in 2001 and there are local and foreign ethnic markets for the fish.

Article text: Wikipedia contributors, Hoplosternum littorale (source revision). Licensed under CC BY-SA 4.0. Retrieved 2026-10-11.

Diet and feeding

The FishTraits compilation records these diet categories for this species: detritus or unidentified plant material; invertebrates or larval fish. These are broad categories, not a claim that every individual consumes every example in a category.

Habitat preferences

Reported habitat associations include creeks.

The source records associations with muck, clay or silt, vegetation, organic debris. An association indicates reported use, rather than an exclusive requirement.

Reproduction and parental care

The compilation reports a representative maturity age of 1 years. Its maturity field summarizes mean, median, or modal estimates, usually for females; male estimates can be used when female data are unavailable. It is not a fixed age at which every fish first breeds.

Batch or serial spawning has been reported somewhere in the species’ range. This does not establish the same spawning pattern for every population.

Recorded spawning months are Jan, Feb, Mar, Apr for the source’s reporting region (French Guiana). This is a regional calendar, not a range-wide schedule.

Size and recorded longevity

FishTraits reports a maximum total length of 24 centimetres. Some entries use an estimated asymptotic length; this value should not be treated as a certified record catch.

Recorded longevity in the compilation is 4 years. Wild observations were preferred, but captive records were accepted where wild records were unavailable, and unspecified records were assumed wild. The value is not a guaranteed wild lifespan or an aquarium life expectancy.

Native range

Tropical America. Occurs in Trinidad, and is widespread in South America east of the Andes and north of Buenos Aires, including the Rio Orinoco, coastal rivers of the Guianas, Rio Amazonas basin, Rio Paraguay, lower Rio Parana and coastal systems in southern Brazil (Reis 1997).

Habitat and ecology

Brown hoplos are sexually dimorphic, with males larger than females and possessing enlarged pectoral fin spines and adjacent fat deposits during the reproductive season. These enlarged spines are used in aggressive or defensive encounters (Winemiller 1987; Hostache and Mol 1998). Nico and Muench (2004) describe nesting habits of this species in Florida. Spawning season in Florida occurrs from May to September, coinciding with the rainy season and generally higher water levels and temperatures, and similar to the timing of the reproductive season in the native range (Winemiller 1987). Numbers of bubble nests and gonadosomatal indices (GSI) for both males and females peak in August-September (Nico and Muench 2004; Gestring et al. 2009).

Introduction history

Unknown. Possibly released food fish, aquarium release, or escape from aquaculture ponds. Expanded range around Florida may have been assisted by humans to establish both commercial and subsistence fisheries (Gestring et al. 2009).

Ecological impacts

Duxbury et al. (2010) found that H. littorale reduced both abundance and diversity of aquatic macroinvertebrates in experimental enclosures.

Stevens et al. (2010) found that H. littorale was an important part of the diet of Common Snook (Centropomus unidecimalis) in the tidal freshwater portion of the Peace River immediately following Hurricane Charley in 2004. It is also consumed by other large piscivores, including Largemouth Bass (Micropterus salmoides), Butterfly Peacock Bass (Cichla ocellaris), alligators, Double-crested Cormorant (Phalacrocorax auritus), and Great Blue Heron (Ardea herodias) (Gestring et al. 2009).

Range

Where it lives

Share of 444 GBIF observation records with a state location, across 1 states.
0%
100%
Share of 444 GBIF observation records with a state location, across 1 states.

Share of records by state

Habitat

Water and movement

Water
WoRMS records this species in fresh water.
USGS NAS habitat
Freshwater
US status
Exotic — the USGS Nonindigenous Aquatic Species database lists it as introduced from outside North America.
Migration
Not migratory

Classification

Taxonomy

Kingdom
Animalia
Phylum
Chordata
Superclass
Actinopterygii
Class
Teleostei
Order
Siluriformes
Genus
Hoplosternum
Species
Hoplosternum littorale
ITIS TSN
679689
WoRMS AphiaID
1014873
GBIF key
2342499

Common questions about Brown Hoplo

What is the scientific name of Brown Hoplo?
The scientific name is Hoplosternum littorale, in the family Callichthyidae. Classification follows ITIS.
Does Brown Hoplo live in fresh water or salt water?
WoRMS records this species in fresh water.
Where has Brown Hoplo been recorded in the United States?
GBIF has observations in 1 states, with the most records in Florida. The map shows observation records, which do not establish the complete natural range.