Asian Swamp Eel

Monopterus albus

Synbranchidae · freshwater and saltwater and brackish water fish

12 minute read · Species guide

Asian Swamp Eel field guide illustration

About Asian Swamp Eel

The Asian swamp eel (Monopterus albus), also known as rice eel, ricefield eel, rice paddy eel, or white rice-field eel, is a commercially important, air-breathing species of fish in the family Synbranchidae. It occurs in East and Southeast Asia, where it is commonly sold and eaten throughout the region. It has been introduced to two areas near the Everglades in Florida and near Atlanta, Georgia.

Taxonomy

The Asian swamp eel is a freshwater, eel-like fish belonging to the family Synbranchidae (swamp eels). Some work indicates that the species should be split into three geographical clades or cryptic species, although these were not given systemic names, as the taxonomic synonymy was too complex to sort out at the time. The populations in the Ryukyus are distinct, the populations in China and Japan belong to another clade, and the rest, the original M. albus, belong to the third group. Although these groups are too phenotypically similar to tell apart morphologically, they exhibit different brooding behaviours. In the Japanese/Chinese form, the males wait until the fertilised eggs hatch in their foam nests, and then keep the larvae in their mouths until they can breathe their own air. The Ryukyuan populations also make foam nests, but do not keep the larvae in the somewhat narrow buccal cavities in their mouths. The most widespread clade does not make foam nests, but lays the eggs among the roots of floating plants and shows no parental care. Larvae use their pectoral fins to increase water flow and thus oxygen intake across their skin. This last form shows the most genetic diversity and may belong to numerous cryptic species. This form is also the type that has been introduced to the USA.

M. albus is not a "true" eel' in the order Anguilliformes; it belongs to the order Synbranchiformes.

Description

The Asian swamp eel has a scaleless, anguilliform body that grows to a meter or less, typically 25 to 40 cm as an adult. As a swamp eel, it has a tapering tail and blunt snout and lacks pectoral and pelvic fins. The dorsal, anal, and caudal fins are rudimentary, with the caudal fin often absent. These fins serve to protect the swamp eel against rolling and assist in sudden turns and stops. Its gill membranes are fused, but one V-shaped gill is located beneath the head. Such a shape prevents reverse flow.

Their color is variable, but generally olive or brown, with irregular dark flecks. Individuals in Florida usually have a dark body and head, with dark olive or brown dorsal coloring and light orange ventral coloring. Individuals caught in Florida can be more colourful, indicating breeding for the pet trade.

The mouth is large and protractile, and both upper and lower jaws have tiny teeth for eating fishes, worms, crustaceans, and other small, aquatic animals.

Similar species

M. cuchia, a related species also commonly eaten, has also been introduced to the USA. When it breaths, the throat expands on sides of head, as opposed to ventrally in M. albus. This species also has "suprapharyngeal air chambers", which M. albus does not, and a few scales, which are entirely absent in M. albus. M. cuchia has a single row of teeth, as opposed to two rows.

Distribution

It has a wide distribution. Monopterus albus is native to much of East and Southeast Asia, ranging west as far as India. M. albus is native to the tropical and subtropical areas of northern India and Burma to China, Japan, and Indo-Malayan Archipelago, possible populations in Far East Russia and northeastern Australia might belong to different cryptic species. It is a common fish in India, Southern China to Malaysia and Indonesia.

The populations in most of Japan (Honshu and Kyushu) are likely introduced from China. The population in the Nara Basin was introduced from Korea in the beginning of the 20th century. Its distribution in Japan is discontinuous, which also indicates that it is introduced within the last millennium or so. The eels found in Taiwan appear to belong to two different species, a Japanese form was introduced in 1940, but a Southeast Asian form is also common and may have also been introduced or be native. The eels were first introduced to Oahu in the Hawaiian Islands around 1900, where they still occur. Earliest record of the fish in the Philippines is in 1918 from a collection by the Commercial Museum of Philadelphia where it has become an invasive species.

Locations in the Southeastern United States were not colonized until the end of the 20th century. Around 1990, the eels were introduced to several ponds at a nature center near Atlanta, Georgia, within the Chattahoochee River drainage basin; by 1994, individuals had migrated to an adjacent marsh, the Chattahoochee Nature Center north of Atlanta. Subsequently, eels were collected from Florida waters in 1997 at two widely separated areas, one in southeast and the other in west-central Florida. Tens of thousands of swamp eels are estimated to inhabit nearly 55 miles of two water canal systems in southern Florida, one in the North Miami area and another on the eastern side of Everglades National Park. Two other populations of the eels have been discovered since 1993, one outside of Tampa, Florida, and one in southern Georgia near the Chattahoochee River. One or more of the populations are believed to be the result of an intentional or accidental release of the creature from a home aquarium or fish farm. Some populations may have been the result of an attempt by a few local residents to establish the eels as a food source.

Ecology

M. albus is a nocturnal animal. Its diet includes other fish, shrimp, crayfish, frogs, turtle eggs, aquatic invertebrates such as worms and insects, and occasionally detritus.

An old document from 1958 claimed M. albus is capable of moving over dry land, but many years of study found no evidence for this.

Habitat

The preferred environment for the Asian swamp eel includes a wide variety of muddy, freshwater, shallow wetlands, such as rice paddies, ditches, ponds, marshes, streams, rivers, canals, lakes, and reservoirs. Depths less than 3 m are optimal. M. albus can live in a wide range of oxygen levels. This fish can obtain up to 25% oxygen from air transcutaneously if not using gills under water.

Lifecycle

The Asian swamp eel is sequentially hermaphroditic. All young are females. As juvenile fish begin to mature, some take on the masculine phenotype. Males are capable of changing sex, allowing them to replenish female populations when female densities are low. This change from one sex to another can take up to a year.

Spawning can occur throughout the year. Some Japanese and Chinese forms of M. albus exhibit a great deal of parental care. Large males construct bubble nests at the mouth of burrows and guard the eggs and young. In some Japanese and Chinese forms, eggs are laid in bubble nests located in shallow waters. These bubble nests float at the water's surface and are not attached to aquatic vegetation. Females produce up to 1,000 eggs, each, per spawning event.

Disease

Swamp eels are a host for the nematode Gnathostoma spinigerum. In Thailand and Vietnam, eating raw or undercooked swamp eel is the most common cause of gnathostomiasis, an uncommon parasitic disease.

Uses

The fish is an important protein source for people in Thailand. It is cultured throughout Vietnam. In Indonesia, Cambodia, China, Laos, Myanmar, Thailand, Vietnam, and other Asian countries, swamp eels are farmed in polyculture rice fields and sold as a food product with the rice crop.

In Balinese, the eels are known as lindung, they are sold dried in almost all village markets for use in Hindu offerings.

In Japan, it is known as ta-unagi, from 田, pronounced "ta", meaning paddy and 鰻, pronounced "unagi", meaning eel, usually written in katakana as タウナギ, and not commonly eaten.

In addition to being useful as a food, this species of eel is also often released into natural water resources in Thailand. According to the belief of the Thai people that it will help to end suffering and sorrow, or as a merit as releasing other fish or other aquatic animals such as climbing perch (Anabas testudineus), striped snakehead (Channa striata), Chinese edible frog (Hoplobatrachus rugulosus), pond snail (Filopaludina martensi), etc.

Conservation

Asian swamp eels might pose a future threat to the environment of Everglades National Park, although preliminary studies reported no deleterious ecological effects in Florida. However, more recent studies in the Everglades do show several species faced precipitous declines after the introduction of swamp eels. Two crayfish became nearly absent from areas with swamp eels, and other species of fish also saw significant declines. The United States Geological Survey has used several methods to control the M. albus population here. They discourage catching and transporting the eel. Water-management structures near established swamp eel populations are not being opened to prevent or at least retard dispersal, particularly into the waters of the park. Adult and juvenile swamp eels are air-breathers, while young absorb oxygen directly through the skin. As such, standard fish poisons or piscicides (e.g., rotenone and antimycin A) that are transmitted across the gill membrane may not be effective. Serial pesticide dilutions of antimycin-A were tested and found to be innocuous. No changes in morbidity and mortality were observed. The fish in the United States likely originate from a different areas in Asia, and are slightly different in characteristics.

Article text: Wikipedia contributors, Asian swamp eel (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: algae or phytoplankton; 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 medium to large rivers, streams and small rivers, creeks.

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

The species is classified as tolerant of a broad range of salinities. This flag does not specify a salinity range for aquarium care.

Size and recorded longevity

FishTraits reports a maximum total length of 100 centimetres. Some entries use an estimated asymptotic length; this value should not be treated as a certified record catch.

Spawning movements

The compilation records significant spawning-related movement. Its combined migration flag covers movements within fresh water as well as between rivers and the sea; this flag alone does not establish which migration pattern applies.

Identification and appearance

Identifying characteristics and illustrations or photographs were given by Day (1958), Sterba (1973), Rosen and Greenwood (1976), Masuda et al. (1984), Talwar and Jhingran (1992), and Kottelat et al. (1993); characteristics were also provided by Smith (1945) and Merrick and Schmida (1984). This eel was included in keys of Rosen and Greenwood (1976), Talwar and Jhingran (1992), and Kottelat et al. (1993).

Most individuals in Florida are olive-drab brown in color with yellow-orange bellies (as shown above). However, some specimens are brightly colored with variations of orange, pink, and a calico pattern (Shafland et al. 2010).

Asian Swamp Eel is very morphologically similar to another introduced synbranchid, Cuchia (M. cuchia), and can be distinguished by the following characters (Nico et al. 2019):

Native range

Genetic analysis indicates that there have been multiple introductions from different geographic areas (Collins et al. 2002). The Atlanta population is from Japan or Korea; Florida populations in Tampa and North Miami are from Southern China while the population in Homestead is from Indo-China, the Malay Peninsula, or the East Indies (Collins et al. 2002).

Habitat and ecology

This species is a sequential hermaphrodite: all individuals are born and mature as females and some later transform into males (Liem 1963; Shafland et al. 2010). Populations studied in south Florida tend to be heavily skewed towards females (90-98%; Shafland et al. 2010). In Snake Creek, individuals transitioning ranged in size from 694-782 mm TL, whereas the smallest male observed at another location was 434 mm TL. The smallest mature female was 318 mm TL and the smallest mature male was 434 mm TL (Shafland et al. 2010). A mature female averaged 439 (range 268-642) eggs (Shafland et al. 2010).

Laboratory studies show that swamp eels stopped feeding at 14-16ºC and died at 8-9ºC (Shafland et al. 2010). This temperature coincides with a range that would not extend farther north than Jacksonville, Florida (Shafland and Pestrak 1982). However, the Georgia population has survived air temperatures below freezing and ice cover over their pond habitat (Starnes et al. 1998) for many years indicating that it is different genetically (as determined by Collins et al. 2002). Collins et al. (2002) predicted these ecological differences based on genetics.

This species can breathe air, using atmospheric oxygen absorbed via a vascularized breathing apparatus at the rear of their mouths (Shafland et al. 2010).

Long and LaFleur (2011) used otoliths to estimate average daily growth rates and hatching dates for juvenile swamp eels in the Chattahoochee River, Georgia population, with an estimated growth rate of 0.2 cm/day.

Introduction history

Its introduction into Florida was probably the result of either an aquarium release, a fish farm escape or release, or release of specimens from the live food-fish market. The Tampa population is near a former fish farm. Colorful specimens may indicate selective breeding for the aquarium trade. They are a popular ethnic food item and may have been released by that trade. The eel was probably introduced into Georgia as an aquarium release. In Georgia, adults were first collected in 1994, although they were likely present since 1990 or before (Starnes et al. 1998; Turkewitz 2006). It was presumably brought to Hawaii by Asian immigrants as a food fish (Devick 1991b). Brock (1960) stated that it was established in Hawaii prior to 1900. Devick (1991b) listed it as one of six fish species that were successfully introduced into Hawaii in the 19th century. However, Cobb (1902) and Jordan and Evermann (1902, 1905) made no mention of finding the species in their turn-of-the-century surveys of Hawaiian fishes.

Ecological impacts

Summary of species impacts derived from literature review. Click on an icon to find out more... Using a 26 year dataset in the Florida Everglades, Pintar et al. (2023) found that Monopterus albus / javenensis reduced the population of the crayfishes Procambarus alleni and P. fallax by >99%, and of the fishes Jordanella floridae by >99%, Fundulus confluentus by >90%, and F. chrysotus and Gambusia holbrooki by >50%. In both Georgia and Florida there is concern that the species will spread to adjacent water bodies as has occurred in the Everglades region of Florida (Kline et al. 2013). The Georgia impoundments are connected to the Chattahoochee River. Shafland et al. (2010) studied swamp eel populations established in south Florida and reported no deleterious ecological effects, although it should be noted that the investigators focused on populations inhabiting canals and associated waterways, habitats already highly disturbed. In addition, their study was largely interested in possible harm caused by swamp eels to sport fishes. Nico et al. (2011) examined the occurrence of internal parasites in both imported, wild-caught swamp eels from a U.S. retail food market and from an introduced population in Florida, finding parasites in nearly all specimens and highlighting the potential of Monopterus as a vector for introduction of macroparasites. Asian Swamp Eels are a known host of multiple Gnathostoma spp. nematodes, and are a potenial source of gnathostomiasis in humans (Cole et al. 2014).

Range

Where it lives

Share of 157 GBIF observation records with a state location, across 7 states.
0%
86%
Share of 157 GBIF observation records with a state location, across 7 states.

Habitat

Water and movement

Water
WoRMS records this species in fresh water, brackish water and the sea.
USGS NAS habitat
Freshwater
US status
Exotic — the USGS Nonindigenous Aquatic Species database lists it as introduced from outside North America.
Migration
Migratory
Pattern

Classification

Taxonomy

Kingdom
Animalia
Phylum
Chordata
Superclass
Actinopterygii
Class
Teleostei
Order
Synbranchiformes
Genus
Monopterus
Species
Monopterus albus
ITIS TSN
166697
WoRMS AphiaID
281590
GBIF key
5204081

Common questions about Asian Swamp Eel

What is the scientific name of Asian Swamp Eel?
The scientific name is Monopterus albus, in the family Synbranchidae. Classification follows ITIS.
Does Asian Swamp Eel live in fresh water or salt water?
WoRMS records this species in fresh water, brackish water and the sea.
Where has Asian Swamp Eel been recorded in the United States?
GBIF has observations in 7 states, with the most records in Florida, Georgia, Texas. The map shows observation records, which do not establish the complete natural range.

Closest relatives

Other Monopterus species

Same family

More Synbranchidae