Himantura chaophrayaFreshwater whipray(Also: Giant Freshwater Stingray)

Ge­o­graphic Range

Giant fresh­wa­ter stingrays are found in the large river sys­tems of Thai­land, in­clud­ing the Mekong, Chao Phraya, Nan, Bang Kapong, Prachin Buri, and Tapi River basins. They are also found in the Kin­abatan­gan River in Malaysia, as well as the is­land of Bor­neo (in the Ma­hakam River). (Last and Man­jaji-Mat­sumoto, 2008; Monkol­pr­a­sit and Roberts, 1990; Rain­both, 1996)

Habi­tat

This species is typ­i­cally found over sandy bot­toms in large rivers, at depths of 5 to 20 me­ters. Many fe­males are found in es­tu­ar­ies and it is thought that they give birth in brack­ish wa­ters, though the rea­son for this is not cur­rently known. There are no records of this species from fully ma­rine habi­tats. (Marzullo, et al., 2011; Vidthayanon, et al., 2011)

  • Range depth
    5 to 20 m
    16.40 to 65.62 ft

Phys­i­cal De­scrip­tion

Like other stingray species, giant fresh­wa­ter stingrays are char­ac­ter­ized by their large oval shape and long tails. In­di­vid­u­als have been recorded to reach weights of 600kg and lengths of 300 cm in total length (one third of which was con­tributed by the tail). The tail is very smooth on the dor­sal side, but the ven­tral side has a spine with saw-like ser­ra­tions and an as­so­ci­ated venom gland. Two pelvic fins are found on ei­ther side of the tail, with the pri­mary trait dis­tin­guish­ing males and fe­males being the pres­ence of a clasper on each male pelvic fin. These pe­nis-like struc­tures re­lease sperm dur­ing cop­u­la­tion. This species’ oval shape is formed by the pec­toral fins, which ex­tend an­te­ri­orly to join with the snout. The pec­toral fins con­tain 158-164 pec­toral ra­di­als, which are small bone-like struc­tures that sup­port the large fins. Over­all, the body is rel­a­tively flat. The mouth is lo­cated on the un­der­side of the disk and is com­prised of two jaws filled with small teeth, and lips cov­ered with small papil­lae, which are sim­i­lar to taste buds. Two par­al­lel rows of gill slits are found pos­te­rior to the mouth. The col­oration dis­plays the coun­ter­shad­ing pat­tern is typ­i­cal of many aquatic an­i­mals. The dor­sum is darkly col­ored, pre­vent­ing preda­tors swim­ming above them from see­ing them against the sand, while the lighter col­ored belly ob­scures an in­di­vid­u­als body out­line from preda­tors below, due to in­com­ing sun­light. (Fyler and Caira, 2006; Lund­berg, et al., 2000; Vidthayanon, et al., 2011)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    600 (high) kg
    1321.59 (high) lb
  • Range length
    300 (high) cm
    118.11 (high) in

De­vel­op­ment

Lit­tle is known about the de­vel­op­ment of giant fresh­wa­ter stingrays. How­ever, it is likely sim­i­lar to that of a re­lated species, Dasy­atis sabina (At­lantic stingray). In At­lantic stingrays, de­vel­op­ment takes ap­prox­i­mately 12 weeks. For the first 4 to 6 weeks, the em­bryo elon­gates but there is no head or body de­vel­op­ment. After 6 weeks, gills begin to grow and the fins and eyes begin to de­velop. The tail and spine ap­pear shortly be­fore hatch­ing and at birth, stingrays look like minia­ture adults. The av­er­age disc width of newly hatched young is 30 cm. (John­son and Snel­son, 1996; Luna and Wi­ethuchter, 2011)

Re­pro­duc­tion

Fe­male stingrays ap­pear to choose mates by using their elec­trosen­sory sys­tem to de­tect sex-spe­cific elec­tri­cal sig­nals pro­duced by males. Once a fe­male has mated, they leave the male and re­side with other fe­males in brack­ish wa­ters until they give birth. Males have a clasper (a cop­u­la­tory struc­ture that holds sperm) at­tached to each pelvic fin. Hav­ing mul­ti­ple claspers al­lows a male stingray to im­preg­nate a fe­male with one clasper and then seek out an­other fe­male to im­preg­nate with the re­main­ing clasper. Male stingrays pro­duce and store sperm through­out the year to en­sure that they have suf­fi­cient sperm for use dur­ing the mat­ing sea­son. (John­son and Snel­son, 1996)

Very lit­tle is known re­gard­ing the re­pro­duc­tive cycle of giant fresh­wa­ter stingrays in the wild. Cap­tive breed­ing ef­forts have in­di­cated that preg­nant fe­males give birth to 1 to 2 off­spring per breed­ing event. How­ever, other in­for­ma­tion from cap­tive breed­ing pro­grams is sparse and most of these pro­grams have been dis­con­tin­ued. (Fowler, et al., 2005)

  • Breeding interval
    Frequency of breeding in giant freshwater stingrays is currently unknown
  • Breeding season
    The seasons in which fertilization and birth occur are currently unknown
  • Range number of offspring
    1 to 2

Male stingrays pro­vide no parental in­vest­ment to their off­spring after mat­ing. Fe­males give birth to live young in es­tu­ar­ine birthing grounds. They then take care of their newly hatched young until they are roughly one-third the size of the fe­male, at which point they are con­sid­ered ma­ture and will move to com­pletely fresh­wa­ter habi­tats. (John­son and Snel­son, 1996)

  • Parental Investment
  • female parental care
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female
  • pre-independence
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

There is lit­tle in­for­ma­tion re­gard­ing the lifes­pan of this species. How­ever, other mem­bers of the genus Hi­man­tura have been re­ported to live 5 to 10 years in the wild. This species fares poorly in cap­tiv­ity, due to the dif­fi­cul­ties as­so­ci­ated with pro­vid­ing proper food and space. (Com­pagno and Cook, 1995; Last and Stevens, 2009; Vidthayanon, et al., 2011)

Be­hav­ior

Giant fresh­wa­ter stingrays are so­cial, seden­tary an­i­mals that gen­er­ally stay in one area and within a par­tic­u­lar group. They are likely able to com­mu­ni­cate with con­specifics via elec­tri­cal im­pulses sent through the body, as has been found in other stingray species. There have been at­tempts to ex­am­ine the range and move­ment using tag­ging stud­ies, but no suc­cess­ful re­sults were col­lected from this ex­per­i­ment. (Vidthayanon, et al., 2011)

Home Range

Giant fresh­wa­ter stingrays gen­er­ally stay in the same river sys­tem in which they were hatched, but the av­er­age size of an in­di­vid­ual's day to day range is cur­rently un­known. (John­son and Snel­son, 1996)

Com­mu­ni­ca­tion and Per­cep­tion

In­traspe­cific com­mu­ni­ca­tion has not yet been stud­ied in this species, but sim­i­lar species of stingrays have been doc­u­mented to com­mu­ni­cate by gen­er­at­ing and sens­ing species- and con­text-spe­cific elec­tri­cal im­pulses. Stingrays have an ex­ten­sive elec­trosen­sory sys­tem that in­cludes many re­cep­tive or­gans known as Am­pul­lae of Loren­zini. There are pores all over the stingray’s body lead­ing to canals under the skin. Each pore is full of many sen­sory re­cep­tor cells. The arrange­ment of the pores al­lows the stingray to de­tect move­ment of prey and preda­tors via the elec­tri­cal fields that these move­ments gen­er­ate. Stingrays can also per­ceive their en­vi­ron­ment vi­su­ally, al­though this species does not rely on this sense as much be­cause they are found in areas that are dark and full of sed­i­ment. Like other stingray species, giant fresh­wa­ter stingrays also have well-de­vel­oped senses of smell and hear­ing, as well as a lat­eral line sys­tem for de­tect­ing vi­bra­tions in the water (Hart, et al., 2011; Sis­neros and Tri­cas, 2002)

Food Habits

Giant fresh­wa­ter stingrays gen­er­ally feed on river bot­toms. Their mouth con­tains two jaws that act like crush­ing plates, and small teeth to con­tinue chew­ing up food. Their diet con­sists mainly of ben­thic fishes and in­ver­te­brates. (Luna and Wi­ethuchter, 2011; Vidthayanon, et al., 2011)

  • Animal Foods
  • fish
  • mollusks
  • aquatic or marine worms
  • aquatic crustaceans

Pre­da­tion

Adult giant fresh­wa­ter stingrays, as the largest or­gan­isms in their habi­tats, have few nat­ural preda­tors. Their coun­ter­shaded color pat­tern and seden­tary lifestyle offer even small in­di­vid­u­als pro­tec­tion from larger preda­tors, as they are able to blend in with the river bot­tom. When swim­ming above the bot­tom, their light-col­ored un­der­side al­lows them to be hid­den from preda­tors, due to the sun­light from above. This species also has a strong, ser­rated, ven­omous spine on its tail, which can be used in self de­fense. The only major preda­tor of giant fresh­wa­ter stingrays is hu­mans. In Thai­land, fish­er­men seek out these an­i­mals for food, per­sonal aquar­i­ums, and sport. (Vidthayanon, et al., 2011)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Giant fresh­wa­ter stingrays act as preda­tors of smaller an­i­mals liv­ing on or in the river floor. A large num­ber of ces­tode species (tape­worms) have been de­scribed from the in­tes­tine of this species, which is thought to be their only host. The mode of trans­mis­sion for these tape­worms is cur­rently un­known. (Fyler and Caira, 2006; Healy, 2006)

Com­men­sal/Par­a­sitic Species
  • Rhineboth­rium kin­abatan­ga­nen­sis (Class Ces­toda, Phy­lum Platy­helminthes)
  • Rhineboth­rium mega­can­thophal­lus (Class Ces­toda, Phy­lum Platy­helminthes)
  • Rhineboth­rium abaien­sis (Class Ces­toda, Phy­lum Platy­helminthes)
  • Acan­thoboth­rium as­ni­hae (Class Ces­toda, Phy­lum Platy­helminthes)
  • Acan­thoboth­rium etini (Class Ces­toda, Phy­lum Platy­helminthes)
  • Acan­thoboth­rium mas­ni­hae (Class Ces­toda, Phy­lum Platy­helminthes)
  • Acan­thoboth­rium sa­liki (Class Ces­toda, Phy­lum Platy­helminthes)
  • Acan­thoboth­rium zainali (Class Ces­toda, Phy­lum Platy­helminthes)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Giant fresh­wa­ter stingrays are a food source in some Asian cities, even though it is now il­le­gal to fish for this en­dan­gered species. They are also col­lected for aquar­i­ums and are a pop­u­lar sport fish. (Com­pagno and Cook, 1995; Rain­both, 1996; Vidthayanon, et al., 2011)

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

When fish­er­men try to catch giant fresh­wa­ter stingrays, they will whip their tail (bear­ing its large, ser­rated, ven­omous spine) to try and get away. These spines have been re­ported to be strong enough to go through wooden boats. There have been no re­ports of un­pro­voked at­tacks. (Monkol­pr­a­sit and Roberts, 1990)

  • Negative Impacts
  • injures humans

Con­ser­va­tion Sta­tus

Due to rapidly de­clin­ing num­bers of giant fresh­wa­ter stingrays, the IUCN Red List has de­clared this species to be en­dan­gered. In Thai­land, cap­tive breed­ing ef­forts are un­der­way to re­build the pop­u­la­tion, though rates of sur­vival in cap­tiv­ity are very low. Sci­en­tists are work­ing to tag the re­main­ing stingrays in order to un­der­stand their move­ment pat­terns and im­prove con­ser­va­tion ef­forts, but suf­fi­cient re­sults are still lack­ing. (Vidthayanon, et al., 2011)

Con­trib­u­tors

Kelsey Thomp­son (au­thor), Rad­ford Uni­ver­sity, Karen Pow­ers (ed­i­tor), Rad­ford Uni­ver­sity, Kier­sten Newtoff (ed­i­tor), Rad­ford Uni­ver­sity, Melissa Whistle­man (ed­i­tor), Rad­ford Uni­ver­sity, Je­remy Wright (ed­i­tor), Uni­ver­sity of Michi­gan-Ann Arbor.

Glossary

acoustic

uses sound to communicate

benthic

Referring to an animal that lives on or near the bottom of a body of water. Also an aquatic biome consisting of the ocean bottom below the pelagic and coastal zones. Bottom habitats in the very deepest oceans (below 9000 m) are sometimes referred to as the abyssal zone. see also oceanic vent.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

brackish water

areas with salty water, usually in coastal marshes and estuaries.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

coastal

the nearshore aquatic habitats near a coast, or shoreline.

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

ecotourism

humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

electric

uses electric signals to communicate

estuarine

an area where a freshwater river meets the ocean and tidal influences result in fluctuations in salinity.

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

food

A substance that provides both nutrients and energy to a living thing.

freshwater

mainly lives in water that is not salty.

indeterminate growth

Animals with indeterminate growth continue to grow throughout their lives.

internal fertilization

fertilization takes place within the female's body

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

molluscivore

eats mollusks, members of Phylum Mollusca

motile

having the capacity to move from one place to another.

natatorial

specialized for swimming

native range

the area in which the animal is naturally found, the region in which it is endemic.

nocturnal

active during the night

oriental

found in the oriental region of the world. In other words, India and southeast Asia.

World Map

ovoviviparous

reproduction in which eggs develop within the maternal body without additional nourishment from the parent and hatch within the parent or immediately after laying.

piscivore

an animal that mainly eats fish

polygynous

having more than one female as a mate at one time

seasonal breeding

breeding is confined to a particular season

sedentary

remains in the same area

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

social

associates with others of its species; forms social groups.

tactile

uses touch to communicate

tropical

the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.

venomous

an animal which has an organ capable of injecting a poisonous substance into a wound (for example, scorpions, jellyfish, and rattlesnakes).

vibrations

movements of a hard surface that are produced by animals as signals to others

visual

uses sight to communicate

Ref­er­ences

Mur­doch Uni­ver­sity. Sta­tus of fresh­wa­ter and es­tu­ar­ine Elas­mo­branchs in North­ern Aus­tralia. 0642553378. Aus­tralia: Nat­ural Her­itage Trust. 2003. Ac­cessed Feb­ru­ary 05, 2012 at http://​www.​environment.​gov.​au/​coasts/​publications/​pubs/​elasmo-north.​pdf.

Com­pagno, L., S. Cook. 1995. "Sta­tus of the giant fresh­wa­ter stingray (whipray) Hi­man­tura chaophraya (Monkol­pr­a­sit and Roberts 1990)" (On-line). Ac­cessed Feb­ru­ary 05, 2012 at http://​www.​flmnh.​ufl.​edu/​fish/​organizations/​ssg/​sharknews/​sn5/​shark5news7.​htm.

Fowler, S., R. Ca­vanagh, M. Camhi, G. Burgess, G. Cail­liet, S. Ford­ham, C. Simpfendor­fer, J. Mu­sick. 2005. Sharks, Rays and Chi­maeras: The Sta­tus of the Chon­drichthyan Fishes. Sta­tus Sur­vey. Gland, Switzer­land and Cam­bridge, UK: IUCN/SSC Shark Spe­cial­ist Group.

Fyler, C., J. Caira. 2006. Five new species of Acan­thoboth­rium (Tet­ra­phyl­lidea: On­choboth­ri­idae) from the fresh­wa­ter stingray Hi­man­tura chaophraya (Ba­toidea: Dasy­ati­dae) in Malaysian Bor­neo. The Jour­nal of Par­a­sitol­ogy, 92/1: 105-125.

Hart, N., T. Lin­sey, S. Collin. 2011. Vi­sual com­mu­ni­ca­tion in Elas­mo­brachs. Com­mu­ni­ca­tion in Fishes, 13:1: 337-383.

Healy, C. 2006. Three new species of Rhineboth­rium (Ces­toda: Tet­ra­phyl­lidea) from the fresh­wa­ter whipray, Hi­man­tura chaophraya, in Malaysian Bor­neo. The Jour­nal of Par­a­sitol­ogy, 92/2: 364-374.

John­son, M., F. Snel­son. 1996. Re­pro­duc­tive life his­tory of the At­lantic stingray, Dasy­atis sabina (pisces, Dasy­ati­dae), in the fresh­wa­ter St. Johns River, Florida. Bul­letin of Ma­rine Sci­ence, 59/1: 74-88.

Last, P., B. Man­jaji-Mat­sumoto. 2008. Hi­man­tura da­lyen­sis sp. nov., a new es­turine whipray (Mylio­ba­toidei: Dat­sy­ati­dae) from north­ern Aus­tralia. Pp. 283-291 in P Last, W White, J Pogonoski, eds. De­scrip­tions of new Aus­tralian Chon­drichthyans, Vol. CSIRO Ma­rine and At­mos­pheric Re­search Paper No. 022. Ho­bart, Tas­ma­nia: CSIRO Ma­rine and At­mos­pheric Re­search.

Last, P., J. Stevens. 2009. Sharks and Rays of Aus­tralia. Aus­tralia: CSIRO.

Luna, S., A. Wi­ethuchter. 2011. "Hi­man­tura chaophraya Monkol­pr­a­sit & Roberts, 1990 fresh­wa­ter whipray" (On-line). Ac­cessed Feb­ru­ary 05, 2012 at http://​www.​fishbase.​org/​summary/​Himantura-chaophraya.​html.

Lund­berg, J., M. Kot­te­lat, G. Smith, M. Sti­assny, A. Gill. 2000. So many fishes, so lit­tle time: An overview of re­cent ichty­olog­i­cal dis­cov­ery in con­ti­nen­tal wa­ters. Mis­souri Botan­i­cal Gar­den, 87/1: 26-62.

Marzullo, T., B. Wueringer, L. Jnr, S. Collin. 2011. De­scrip­tion of the mechanore­cep­tive lat­eral line and elec­trore­cep­tive am­pullary sys­tems in the fresh­wa­ter whipray, Hi­man­tura da­lyen­sis. Ma­rine and fresh­wa­ter re­search, 62/6: 771-779.

Monkol­pr­a­sit, S., T. Roberts. 1990. Hi­man­tura chaophraya, a new giant fresh­wa­ter stingray from Thai­land. Japan­ese Jour­nal of Ichthy­ol­ogy, 37/3: 203-208.

Rain­both, W. 1996. Fishes of the Cam­bo­dian Mekong. Rome, Italy: FAO.

Sis­neros, J., T. Tri­cas. 2002. Neu­roethol­ogy and life his­tory adap­ta­tions of the elas­mo­branch elec­tric sense. Jour­nal of Phys­i­ol­ogy-Paris, 96/5-6: 379-389.

Vidthayanon, C., I. Baird, Z. Hogan. 2011. "Hi­man­tura chaophraya" (On-line). Ac­cessed Feb­ru­ary 05, 2012 at http://​www.​iucnredlist.​org/​apps/​redlist/​details/​195320/​0.