Hubbry Logo
Crab-eating frogCrab-eating frogMain
Open search
Crab-eating frog
Community hub
Crab-eating frog
logo
8 pages, 0 posts
0 subscribers
Be the first to start a discussion here.
Be the first to start a discussion here.
Crab-eating frog
Crab-eating frog
from Wikipedia

Crab-eating frog
Fejervarya cancrivora from Bogor, West Java
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Anura
Family: Dicroglossidae
Genus: Fejervarya
Species:
F. cancrivora
Binomial name
Fejervarya cancrivora
(Gravenhorst, 1829)
Synonyms

Rana cancrivora Gravenhorst, 1829
Rana cancrivora ssp. raja Smith, 1930
Fejervarya raja (Smith, 1930)

The crab-eating frog (Fejervarya cancrivora) is a frog native to south-eastern Asia including Taiwan,[2] China, Sumatra in Indonesia,[3] the Philippines and more rarely as far west as Orissa in India.[4] It has also been introduced to Guam, most likely from Taiwan.[5] It inhabits mangrove swamps and marshes and is one of 144 known modern amphibians which can tolerate brief excursions into seawater, and is possibly the only extant marine amphibian.[6]

This frog can tolerate marine environments (immersion in sea water for brief periods or brackish water for extended periods) by increasing urea production and retention, and by remaining slightly hyperosmotic within urea and sodium flux.[7][8][9] Adults can survive in salt water with salinity as high as 2.8%, and tadpoles can survive salinities as high as 3.9%.[10]

Diet

[edit]

The food sources of the crab-eating frog are mainly determined by the locally available prey. Near fresh water, its diet consists largely of insects. But in an environment with brackish water, small crustaceans, including crabs, form the main part.[11]

Human consumption

[edit]

In Southeast Asia, the crab-eating frog is locally hunted for food and is often farmed for its edible legs, including in Java, Indonesia, where the dish is known as swikee.[12]

See also

[edit]

References

[edit]
[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
The crab-eating frog (Fejervarya cancrivora) is a medium-sized aquatic frog in the family Dicroglossidae, notable for its exceptional tolerance to brackish and saline environments among amphibians. Native to southeastern Asia, it inhabits coastal wetlands where its diet includes small and crustaceans in salty habitats, shifting to near freshwater. Adults reach a snout-vent length of 60–107 mm, with females typically larger (up to 107 mm) than males (up to 80 mm), featuring a robust build, glandular on the head and flanks, discontinuous dorsolateral folds, extensive on the hind feet, and variable dorsal coloration ranging from light to dark brown with mottling and a pale underside. This occupies a range across southeastern Asia, including , , , Brunei Darussalam, and on , and (, , ), following taxonomic revisions delimiting it within the former F. cancrivora complex; introduced populations occur in and . It favors lowland habitats such as mangrove swamps, tidal estuaries, coastal marshes, rice paddies, and prawn ponds, often up to 1,300 m elevation, and demonstrates remarkable osmoregulatory adaptations, surviving salinities up to 2.8% as adults and 3.9% as tadpoles through mechanisms like elevated production. Diet varies by locale: crustaceans (including crabs) predominate in brackish areas, while and small vertebrates form the bulk near freshwater. The crab-eating frog reproduces year-round, with peak activity at the start of the ; males call from water edges or low vegetation with a rapid, gargling advertisement call to attract females, who deposit eggs in floating foam nests that develop into tadpoles capable of tolerating brackish conditions. Classified as Least Concern by the (assessed 2004) due to its distribution, presumed large , and resilience to moderate alteration (including agricultural landscapes), though the assessment predates 2019 taxonomic revisions and may require updating, the species faces no major global threats but is locally collected for food in some regions.

Taxonomy

Etymology

The scientific name of the crab-eating frog is Fejervarya cancrivora. The genus Fejervarya honors the Hungarian herpetologist Géza Fejérváry, as established by István József Bolkay in 1915 when he proposed it as a subgenus of Rana. The specific epithet cancrivora derives from the Latin terms cancer (crab) and vorare (to devour), referencing the frog's propensity to consume small crabs and other crustaceans. The common name "crab-eating frog" stems directly from these observations of its diet in brackish and coastal environments, where it preys on crustaceans including juvenile crabs. This naming highlights a key aspect of its foraging behavior in and estuarine habitats. The species was originally described as Rana cancrivora in 1829 by German zoologist Johann Ludwig Christian Gravenhorst, based on specimens collected from , . Gravenhorst's description appeared in his work Deliciae Musei Zoologici Vratislaviensis, marking the first formal recognition of the .

Classification

The crab-eating frog, Fejervarya cancrivora, is classified within the domain Eukarya; kingdom Animalia; phylum Chordata; subphylum Vertebrata; class Amphibia; subclass ; superorder ; order Anura; suborder ; family Dicroglossidae; subfamily Dicroglossinae; genus Fejervarya; and species F. cancrivora. Originally described as Rana cancrivora by Gravenhorst in 1829, the has accumulated several s over time, including Limnonectes cancrivora and Fejervarya raja (the latter now regarded as a junior based on morphological and genetic evidence). Fejervarya moodiei was previously considered part of the but has been delimited as distinct through integrative . Within the genus Fejervarya, F. cancrivora is a member of the "cancrivora complex," a group of morphologically similar frogs distributed across ; recent genetic analyses using mitochondrial 16S rRNA and COI genes, combined with acoustic and morphological data, have confirmed boundaries and clarified distributions for complex members like F. cancrivora and F. moodiei. The species belongs to Dicroglossidae, a speciose family of over 190 anurans primarily occurring in tropical and subtropical and , characterized by diverse reproductive modes including foam nests and direct development. Its closest relatives are other brackish-tolerant congeners such as F. moodiei, reflecting shared physiological adaptations within the genus. The tolerance for saline environments is a derived trait in Fejervarya, enabling exploitation of coastal habitats uncommon among amphibians.

Description and physiology

Physical characteristics

The crab-eating frog (Fejervarya cancrivora) is a medium-sized anuran with adults exhibiting a snout-vent (SVL) ranging from 60.2 to 107.1 mm. Males typically measure 60.2–79.8 mm SVL, while females are larger at 85.1–107.1 mm SVL. The body is rather slender with a narrow head that is slightly longer than wide, featuring a deep profile and a pointed, beak-like when viewed from above. The interorbital space is flat and narrower than the upper width, contributing to the frog's streamlined morphology. The skin texture is smooth to slightly granular on the dorsal surfaces, with irregular, discontinuous dorsolateral folds running along the back and glandular warts present on the sides of the head and lower flanks. Ventral surfaces are generally smooth, though the chin may bear dense spinules. Hind feet exhibit extensive that reaches the tips, with a moderate webbing formula of I1–1½ II1–2 III1–2 IV2–1 V and a dermal flap on the postaxial side of toe V; front feet lack webbing but have long fingers with pointed tips and some dermal fringes. A supratympanic is present, but parotoid glands are absent. Coloration varies geographically and individually, with the dorsum typically medium to dark brown, olive-green, or grayish, often marked by irregular darker spots, blotches, or bars on the lips and hindlimbs. Flanks are creamy white with dark brown marbling, and the venter is pale whitish or creamy with occasional darker mottling. Some individuals display a light vertebral stripe or light and dark mottling of pale and dark brown. Sexual dimorphism is minimal beyond size differences, though males possess paired vocal sacs with dark brown blotches. Diagnostic features include large eyes with a diameter approximately 60% of the snout length and a distinct, rounded tympanum that is about 90% of the eye , featuring a weakly elevated rim. Relative finger lengths follow the pattern II < IV < I < III, and there are prominent inner metatarsal tubercles on the feet. The head is deeper and the snout more pointed compared to close relatives like Fejervarya limnocharis.

Adaptations to salinity

The crab-eating frog (Fejervarya cancrivora) exhibits the highest salt tolerance among amphibians, enabling survival in brackish waters approaching . Adults can endure external salinities up to 28 parts per thousand (ppt) for extended periods, such as weeks, by elevating plasma concentrations to approximately 0.48 M, which accounts for about 60% of the osmotic balance against external ions. This accumulation, supplemented by trimethylamine N-oxide (TMAO) and free as counteracting solutes, prevents cellular in hyperosmotic environments, a strategy convergent with that of some marine elasmobranchs. Unlike typical urea-excreting amphibians, F. cancrivora upregulates hepatic enzymes like during salinity acclimation to sustain these high levels. Osmoregulatory adaptations in F. cancrivora include enhanced renal of excess salts and reduced permeability across the skin compared to freshwater-bound amphibians. The kidneys produce with osmolarities paralleling plasma but lower content, facilitating net salt removal while minimizing loss. The skin, though permeable to water, shows lower passive influx of sodium and s, limiting loading during immersion in ; frogs behaviorally avoid prolonged full-seawater exposure, preferring salinities below 18 ppt to further reduce osmotic stress. Genomic studies reveal upregulated expression of transporter genes, such as those involved in renal sodium (e.g., ANPEP and AVPR2), which evolved to support these coastal adaptations. In comparison to most amphibians, which are confined to freshwater due to highly permeable skins and limited osmoregulatory capacity, F. cancrivora's traits represent an evolutionary specialization for mangrove and estuarine niches. These mechanisms allow hyperosmotic regulation, where internal osmolarity exceeds that of the environment, contrasting with the hypoosmotic strategies of typical anurans. However, limits exist: the species cannot successfully breed in full seawater (35 ppt), as eggs and early tadpoles require salinities below 10 ppt for viability, though later tadpole stages tolerate up to 35 ppt in laboratory conditions.

Distribution and habitat

Geographic range

The crab-eating frog (Fejervarya cancrivora) is native to parts of , with its confirmed range restricted to extreme (Gulf of Thailand coast), peninsular West , the Indonesian islands of , (), and western , as well as Darussalam. Populations are also extant in Malaysian and , though presence in remains uncertain. The species primarily occupies coastal and lowland areas, generally below 500 m elevation, though records extend up to 1,300 m in some regions like . Recent taxonomic revisions of the F. cancrivora complex, based on genetic analyses, have significantly narrowed the recognized distribution of F. cancrivora sensu stricto, reassigning many former populations to other species such as F. moodiei. Historically, the species was considered more widespread, extending from southern (Guangxi and Hainan provinces), , the , and Indochina (including , , , , and ) eastward to the Andaman and Nicobar Islands in and . These broader reports, predating molecular studies, likely encompassed cryptic species within the complex. Introduced populations have been documented outside the native range, including Guam, where breeding status is unclear but establishment is possible through accidental releases. In Indonesia's Papua region (western New Guinea), the species has been introduced to areas like , , Nabire, and . Rare escapes or intentional introductions may occur in and , though these are not confirmed as established; human-modified landscapes, such as agricultural fields, facilitate potential expansion. Genetic studies reveal regional variations within F. cancrivora, including distinct clades in Indonesian (e.g., , , ) and Thai-Malaysian subpopulations, indicating historical connectivity across Southeast Asian lowlands prior to human impacts. For instance, analyses highlight divergence between Philippine (now often reassigned) and Indonesian lineages, supporting a complex evolutionary history tied to coastal distributions.

Habitat preferences

The crab-eating frog (Fejervarya cancrivora) primarily inhabits coastal lowland environments in southeastern Asia, favoring swamps, tidal marshes, estuaries, and other coastal wetlands where is prevalent. These frogs also occupy agricultural landscapes, including paddies, ditches, and , which provide similar moist conditions and access to shallow waters. They avoid arid uplands and purely freshwater interiors, preferring areas influenced by tidal fluctuations and proximity to the sea. In terms of salinity, F. cancrivora thrives in brackish habitats with salinities ranging from 0 to 39 parts per thousand (ppt), though it is most commonly found in moderate brackish conditions around 14 ppt typical of ecosystems; adults tolerate up to 18 ppt, while tadpoles can endure higher levels up to 35 ppt. This tolerance allows occasional use of freshwater ponds but underscores a strong preference for coastal brackish zones over hypersaline or freshwater-only sites. Their physiological adaptations, such as retention for , enable survival in these variable salinities. Microhabitat preferences include burrowing into mud or sheltering among roots during to avoid and predation, emerging to on the ground or low at night when conditions are cooler and moister. Population densities are often higher in human-disturbed wetlands, such as altered s or agricultural edges, where increased edge habitats provide ample cover and prey resources. Seasonally, abundance peaks during the (typically June to ), when flooding enhances breeding and foraging opportunities, though the species remains active year-round and tolerates periodic inundation in its coastal niches.

Behavior and ecology

Diet and foraging

The crab-eating frog (Fejervarya cancrivora) is an opportunistic , primarily consuming small that reflect the availability in its surrounding . In brackish environments such as mangroves, its diet is dominated by crustaceans, including small from genera like Sesarma and Uca (fiddler crabs), which form the predominant prey items by number and volume. In contrast, populations in freshwater or agricultural settings, such as rice fields, shift toward insects including beetles (Coleoptera), and other , flies (Diptera), and hemipterans, along with occasional arachnids and other small arthropods. No significant plant matter is consumed, emphasizing its strictly carnivorous habits. Foraging behavior is primarily nocturnal and crepuscular, with adults employing a sit-and-wait strategy on the ground or low near edges. Prey capture involves rapid extension of the or direct lunges with the jaws, targeting mobile that venture close. Juveniles focus on smaller arthropods, such as tiny , to accommodate their size limitations. Dietary composition exhibits clear habitat-dependent variation, as documented in studies from Singapore's s—where crustaceans prevail—and Indonesia's west coast agricultural areas, where dominate due to prey abundance. This adaptability underscores the frog's generalist feeding strategy, enabling survival across gradients. In ecosystems, its predation on crustaceans plays a key role in regulating local populations, contributing to trophic balance.

Reproduction and life cycle

The crab-eating frog (Fejervarya cancrivora) exhibits breeding activity primarily during the rainy or , from May to November across much of its Southeast Asian range, when individuals aggregate in temporary water bodies such as ponds and ditches. Although breeding can occur year-round in some populations, it peaks at the onset of the . Males call from water edges using a rapid, gargling advertisement call to attract females during . Females deposit eggs in foam nests constructed on the water surface, with clutch sizes ranging from a few hundred to over a thousand eggs per nest. The , produced by the female during oviposition, protects the eggs from predators and environmental stress. Eggs typically hatch within 4 to 10 days, releasing tadpoles into the below the nest. There is no following egg deposition. Tadpoles are herbivorous and detritivorous, grazing on and in aquatic habitats. The larval period lasts 35 to 45 days under typical conditions, though it can extend to 60 days in cooler environments; development requires for optimal growth and survival, with tolerance up to 24 parts per thousand (ppt) observed in the field but slower development at higher salinities. results in juveniles that reach at 1 to 2 years of age. In , individuals live 4 to 5 years, with females reaching a maximum of 5 years and males 4 years.

Conservation

Status

The crab-eating frog (Fejervarya cancrivora) is classified as Least Concern on the , with the assessment conducted in 2020 (published 2022), owing to its extensive distribution across , adaptability to modified s, and presumed large overall . As of the 2025 IUCN Red List update, the status remains Least Concern. Populations are described as common to abundant within the species' core range, spanning coastal regions from to the and parts of and . The species is common to abundant in suitable s, including agricultural landscapes such as paddies and modified wetlands, due to its tolerance for human-altered environments. However, the overall trend is decreasing due to habitat loss. However, local declines occur in habitats, where habitat degradation affects subpopulations. Regionally, the species is noted as protected in , particularly for populations in the where closely related taxa in the F. cancrivora complex occur. It is not listed under Appendix I, II, or III. Monitoring efforts are ongoing in and the , focusing on trade impacts and distribution in protected coastal areas. Overall population trends are stable across the species' range, though certain subpopulations remain vulnerable to localized pressures; studies from 2023 to 2025 have documented potential range shifts driven by , with modeling indicating habitat gains in higher-elevation areas of , , alongside losses in lowlands.

Threats and protection

The crab-eating frog faces significant threats from , primarily driven by clearance for , coastal , and , which fragment its preferred brackish environments across . Overharvesting for the international food trade exacerbates these pressures, with millions of individuals annually exported from countries like and , where the species dominates wild-caught shipments to markets in and . from pesticides and agricultural runoff in fields and coastal areas further endangers populations by contaminating breeding sites and affecting larval development. Emerging threats include climate change-induced shifts in salinity and rising sea levels, which disrupt the species' osmotic adaptations in coastal habitats and reduce tadpole thermal tolerance under combined stressors. Conservation efforts focus on mangrove habitat restoration to mitigate loss, with community-driven projects in the Philippines successfully replanting thousands of hectares to enhance coastal resilience. Regulated aquaculture farming is promoted in source countries to alleviate pressure on wild populations, alongside calls for stricter international trade oversight to curb unregulated exports. Genetic research on population structure aids management by identifying distinct subpopulations vulnerable to localized threats. However, gaps persist, including insufficient monitoring in remote coastal regions and the absence of species-specific trade regulations, hindering effective protection.

Relationship with humans

Culinary use

The crab-eating frog (Fejervarya cancrivora) is traditionally consumed across , particularly in , , , the , and , where it is hunted from wild populations and increasingly farmed for its edible hind legs, prized for their tender texture and mild flavor. These legs are commonly prepared by over open flames, stir-frying with , ginger, chilies, and , or incorporating into soups and curries, serving as a protein-rich component in rural and urban cuisines. Indonesia stands as a primary exporter of crab-eating frog legs, with Java serving as the main harvesting and farming hub; based on export data up to 2002, estimates indicated 28–142 million frogs exported annually, representing about one-seventh of the total harvest, though export quotas later increased to over 83 million individuals in 2016 before fluctuating to about 60 million in 2022. imports—historically accounting for 83% of Indonesia's shipments—have declined due to stricter regulations. Local markets in the and also feature the species, often sourced from coastal and agricultural areas for domestic consumption. This trade contributes to ecological pressures, including overharvesting that threatens wild populations. Pond-based aquaculture for the crab-eating frog emerged in Indonesia during the 1980s to meet demand and alleviate pressure on wild stocks, involving the rearing of tadpoles and juveniles in controlled brackish-water systems until maturity. However, many operations have faced challenges, including high feed costs and disease outbreaks, leading to inconsistent production and ongoing reliance on wild capture. Animal welfare concerns arise in both wild harvesting and farming, where frogs are frequently skinned alive or subjected to and poor , resulting in high mortality rates. Nutritionally, crab-eating frog legs offer high protein content (approximately 16.4 grams per 100 grams raw) with low fat (0.3 grams per 100 grams) and negligible carbohydrates, making them a lean meat source comparable to ; they are especially valued as a seasonal in rural Southeast Asian communities during periods when frogs are abundant.

and trade

Captive breeding of the crab-eating frog (Fejervarya cancrivora) has been achieved in laboratory and farm settings, where protocols replicate conditions to facilitate acclimation and support research on osmotic regulation. These efforts include rearing in controlled salinities up to 9 parts per thousand, demonstrating high survival and rates that mirror natural estuarine habitats. Such breeding is also employed on farms to supplement trade volumes, though it remains limited compared to wild harvesting and is primarily aimed at restocking rather than large-scale production. In the pet trade, the crab-eating frog is occasionally maintained as an exotic pet owing to its relative hardiness and tolerance for varying salinities, but trade volume is minimal relative to commercial food markets. Suitable enclosures must provide humid environments with semi-aquatic features, such as shallow water pools and moist substrates, to accommodate its preference for mangrove-like conditions. Export quotas from specifically allocate smaller numbers for pet purposes, reflecting the niche demand. The species serves as a key in research on , with studies revealing genetic adaptations like upregulated transporters that enable survival in hyperosmotic environments. Transcriptomic analyses have identified key genes involved in ionic balance, underscoring its unique physiological adaptations among amphibians. In educational contexts, exhibits featuring the crab-eating frog in aquariums emphasize its role in mangrove ecosystems, illustrating adaptations to coastal habitats. Trade regulations in impose export controls, including annual quotas that surged for F. cancrivora in recent years but include provisions for monitored captive-bred specimens to ensure . The species poses minimal invasive risk outside its native Southeast Asian range, as its dependence on brackish habitats limits establishment in freshwater-dominated ecosystems.

References

Add your contribution
Related Hubs
User Avatar
No comments yet.