River dolphin

River dolphins
River dolphins are not a taxon, they are an informal grouping of the infraorder Cetacea

Baiji (Lipotes vexillifer)
Information
Families considered river dolphins
New World range map
Old World range map

River dolphins are a widely distributed group of fully aquatic mammals that reside exclusively in freshwater or brackish water. They are an informal grouping within the group dolphin, which is a paraphyletic group within the infraorder Cetacea. The river dolphins comprise the extant families Platanistidae (the Indian dolphins), Iniidae (the Amazonian dolphins), and Pontoporiidae (the brackish dolphins). There are five extant species of dolphins, and two subspecies. River dolphins, alongside other cetaceans, belong to the clade Cetartiodactyla, with even-toed ungulates, and their closest living relatives the hippopotamuses, having diverged about 40 million years ago.

River dolphins are relatively small compared to other dolphins, having evolved to survive in the warm and strong river currents. They range in size from the 5-foot (1.5 m) long South Asian river dolphin to the 8-foot (2.4 m) and 220-pound (100 kg) Amazon river dolphin. Several species exhibit sexual dimorphism, in that the males are larger than the females. They have streamlined bodies and two limbs that are modified into flippers. River dolphins use their conical-shaped teeth and long beaks to capture fast-moving prey in murky water. They have well-developed hearing that is adapted for both air and water; they do not really rely on vision since the water they swim in is usually very muddy. These species are well-adapted to living in warm, shallow waters, and, unlike other cetaceans, have little to no blubber.

River dolphins are not very widespread; they are all restricted to certain rivers or deltas. This makes them extremely vulnerable to habitat destruction. River dolphins feed primarily on fish. Male river dolphins typically mate with multiple females every year, but females only mate every two to three years. Calves are typically born in the spring and summer months and females bear all the responsibility for raising them. River dolphins produce a variety of vocalizations, usually in the form of clicks and whistles.

River dolphins are rarely kept in captivity; breeding success has been poor and the animals often die within a few months of capture. As of 2015, there are only three river dolphins in captivity.

Taxonomy and evolution

Classification

Main article: List of cetaceans

Four families of river dolphins (Iniidae, Pontoporiidae, Lipotidae and Platanistidae) are currently recognized, comprising three superfamilies (Inioidea, Lipotoidea and Platanistoidea). Platanistidae, containing the two subspecies of South Asian river dolphin, is the only accepted family of Platanistoidea.[1] Previously, many taxonomists had assigned all river dolphins to a single family, Platanistidae, and treated the Ganges and Indus River dolphins as separate species. A December 2006 survey found no members of Lipotes vexillifer (commonly known as the baiji, or Chinese river dolphin) and declared the species functionally extinct. With their disappearance, one of the recently accepted superfamilies, Lipotoidea, has become extinct.[2]

The current classification of river dolphins is as follows:[1][3]

In 2012 the Society for Marine Mammalogy began considering the Bolivian (Inia geoffrensis boliviensis) and Amazonian (Inia geoffrensis geoffrensis) subspecies as full species Inia boliviensis and Inia geoffrensis, respectively; however, much of the scientific community, including the IUCN, continue to consider the Bolivian population to be a subspecies of Inia geoffrensis.[4][5]

In October 2014, the Society for Marine Mammalogy took Inia boliviensis and Inia araguaiaensis off their list of aquatic mammal species and subspecies and currently does not recognize these species-level separations.[4][6]

Evolution

Further information: Evolution of cetaceans
Phylogeny of cetaceans based on cytochrome b gene sequences, showing the distant relationship between Platanista and other river dolphins.

River dolphins are members of the infraorder Cetacea, which are descendants of land-dwelling mammals of the order Artiodactyla (even-toed ungulates). They are related to the Indohyus, an extinct chevrotain-like ungulate, from which they split approximately 48 million years ago.[7] The primitive cetaceans, or archaeocetes, first took to the sea approximately 49 million years ago and became fully aquatic by 5–10 million years later. It is unknown when river dolphins first ventured back into fresh water.[8]

River dolphins are thought to have relictual distributions, that is, their ancestors originally occupied marine habitats, but were then displaced from these habitats by modern dolphin lineages.[9][10] Many of the morphological similarities and adaptations to freshwater habitats arose due to convergent evolution; thus, a grouping of all river dolphins is paraphyletic. Amazon river dolphins are actually more closely related to oceanic dolphins than to South Asian river dolphins.[11] Isthminia panamensis is an extinct genus and species of river dolphin, living 5.8 to 6.1 million years ago. Its fossils were discovered near Piña, Panama.[12][13]

River dolphin has been considered a taxonomic description, suggesting an evolutionary relationship among the group, although it is now known that they form two distinct clades. 'True' river dolphins are descendants of ancient evolutionary lineages that evolved in freshwater environments.[9]

Some species of cetacean live in rivers and lakes, but are more closely related to oceanic dolphins or porpoises and entered fresh water more recently. Such species are considered facultative freshwater cetaceans as they can use both marine and freshwater environments. These include species such as the Irrawaddy dolphin, Orcaella brevirostris, found in the Mekong, Mahakam, the Irrawaddy Rivers, as well as the Yangtze finless porpoise Neophocaena phocaenoides asiaeorientalis.[14]

The tucuxi (Sotalia fluviatilis) in the Amazon River is another species descended from oceanic dolphins; however, it does not perfectly fit the label of 'facultative' either, as it occurs only in fresh water. The tucuxi was until recently considered conspecific with the Guiana dolphin (Sotalia guianensis), which inhabits marine waters. It may also be true for the Irrawaddy dolphin and the finless porpoise that, although the species may be found in both freshwater and marine environments, individual animals found in rivers may not be able to survive in the ocean, and vice versa.[15] The tucuxi is currently classified as an oceanic dolphin (Delphinidae).[16]

The Franciscana (Pontoporia blainvillei) has shown a converse evolutionary pattern, and has an ancient evolutionary lineage in freshwater, but inhabits estuarine and coastal waters.[17]

Biology

Anatomy

River dolphins have a torpedo shaped body with a flexible neck, limbs modified into flippers, non-existent external ear flaps, a tail fin, and a small bulbous head. River dolphin skulls have small eye orbits, a long snout and eyes placed on the sides of the head. River dolphins are rather small, ranging in size from the 5-foot (1.5 m) long South Asian river dolphin to the 8-foot (2.4 m) and 220-pound (100 kg) Amazon river dolphin. They all have female-biased sexual dimorphism, with the females being larger than the males.[18][19] River dolphins are polygynous, meaning male river dolphins typically mate with multiple females every year, but females only mate every two to three years. Calves are typically born in the spring and summer months and females bear all the responsibility for raising them.[19]

River dolphins have conical teeth, used to catch swift prey such as small river fish.[19] They also have very long snouts, with some measuring 23 inches (58 cm), four times longer than most of their oceanic counterparts. They have a two-chambered stomach that is similar in structure to that of terrestrial carnivores. They have fundic and pyloric chambers.[20] Breathing involves expelling stale air from their blowhole, followed by inhaling fresh air into their lungs. They do not have the iconic spout, as this only forms when the warm air exhaled from the lungs meets cold external air, which does not occur in their tropical habitats.[19][21]

River dolphins have a thin layer of blubber, this is due to a lack of necessity. Blubber can help with buoyancy, protection from predators (they would have a hard time getting through a thick layer of fat), energy for leaner times, and insulation from harsh climates. The habitats of river dolphins lack these needs.[19]

Locomotion

River dolphins have two flippers and a tail fin. These flippers contain four digits. Although river dolphins do not possess fully developed hind limbs, some possess discrete rudimentary appendages, which may contain feet and digits. River dolphins are slow swimmers in comparison to oceanic dolphins, which can travel at speeds up to 35 miles per hour (56 km/h); the tucuxi can only travel at about 14 miles per hour (23 km/h).[22] Unlike other cetaceans, their neck vertebrae are not fused together, meaning they have greater flexibility than other non-terrestrial aquatic mammals, at the expense of speed. This means they can turn their head without actually moving their entire body.[23][24] When swimming, river dolphins rely on their tail fins to propel themselves through the water. Flipper movement is continuous. River dolphins swim by moving their tail fins and lower bodies up and down, propelling themselves through vertical movement, while their flippers are mainly used for steering. All species have a dorsal fin.[19]

Senses

Biosonar by cetaceans
River dolphins have very small eyes

The ears of river dolphins have specific adaptations to their aquatic environment. In humans, the middle ear works as an impedance equalizer between the outside air's low impedance and the cochlear fluid's high impedance. In river dolphins, and other cetaceans, there is no great difference between the outer and inner environments. Instead of sound passing through the outer ear to the middle ear, river dolphins receive sound through the throat, from which it passes through a low-impedance fat-filled cavity to the inner ear. The ear is acoustically isolated from the skull by air-filled sinus pockets, which allows for greater directional hearing underwater.[25] Dolphins send out high frequency clicks from an organ known as a melon. This melon consists of fat, and the skull of any such creature containing a melon will have a large depression. This allows river dolphins to produce biosonar for orientation.[19][26]:203–427[27][28] They are so dependent on echolocation that they can survive even if they are blind.[29] Beyond locating an object, echolocation also provides the animal with an idea on the object's shape and size, though how exactly this works is not yet understood. The small hairs on the rostrum of the Amazon river dolphin are believed to function as a tactile sense, possibly to compensate for their poor eyesight.[30]

River dolphins have very small eyes for their size, and do not have a very good sense of sight.[1] In addition, the eyes are placed on the sides of the head, so the vision consists of two fields, rather than a binocular view like humans have. When river dolphins surface, their lens and cornea correct the nearsightedness that results from the refraction of light.[31] They have both rod and cone cells, meaning they can see in both dim and bright light.[31] Most river dolphins have slightly flattened eyeballs, enlarged pupils (which shrink as they surface to prevent damage), slightly flattened corneas and a tapetum lucidum; these adaptations allow for large amounts of light to pass through the eye and, therefore, a very clear image of the surrounding area. They also have glands on their eyelids and an outer corneal layer that act as protection for the cornea.[26]:505–519

Olfactory lobes are absent in river dolphins, suggesting that they have no sense of smell.[26]:481–505

River dolphins are not thought to have a sense of taste, as their taste buds are atrophied or missing altogether. However, some dolphins have preferences between different kinds of fish, indicating some sort of attachment to taste.[26]:447–454

Interactions with humans

Threats

Development

Conservation areas for the baiji along the Yangtze River

Development and agriculture have had devastating impacts on the habitats on river dolphins. The total population of Araguaian river dolphins is estimated to be between 600 to 1,500 individuals, and genetic diversity is limited.[11] The ecology of their habitat has been adversely affected by agricultural, ranching and industrial activities, as well as by the use of dams for hydroelectric power. The inhabited section of the Araguaia River probably extends over about 900 miles (1,400 km) out of a total length of 1,300 miles (2,100 km). The Tocantins river habitat is fragmented by six hydroelectric dams, so the population there is at particular risk.[11] Its probable eventual IUCN status is Vulnerable or worse.[11][32]:54–58

Both subspecies of South Asian river dolphins have been very adversely affected by human use of the river systems in the subcontinent. Irrigation has lowered water levels throughout both subspecies' ranges. Poisoning of the water supply from industrial and agricultural chemicals may have also contributed to population decline. Perhaps the most significant issue is the building of more than 50 dams along many rivers, causing the segregation of populations and a narrowed gene pool in which the dolphins can breed. Currently, three subpopulations of Indus river dolphins are considered capable of long-term survival if protected.[32]:31–32, 37–38[33]

As China developed economically, pressure on the baiji river dolphin grew significantly.[32]:41–46Industrial and residential waste flowed into the Yangtze. The riverbed was dredged and reinforced with concrete in many locations. Ship traffic multiplied, boats grew in size, and fishermen employed wider and more lethal nets. Noise pollution caused the nearly blind animal to collide with propellers. Stocks of the dolphin's prey declined drastically in the late 20th century, with some fish populations declining to one thousandth of their pre-industrial levels.[34] In the 1950s, the population was estimated at 6,000 animals,[35] but declined rapidly over the subsequent five decades. Only a few hundred were left by 1970. Then the number dropped down to 400 by the 1980s and then to 13 in 1997 when a full-fledged search was conducted. On December 13, 2006, the baiji (Lipotes vexillifer) was declared "functionally extinct", after a 45-day search by leading experts in the field failed to find a single specimen. The last verified sighting was in September 2004.[2]

Competition

The region of the Amazon in Brazil has an extension of 3,100,000 sq mi (8,000,000 km2) containing diverse fundamental ecosystems.[36][37] One of these ecosystems is a floodplain, or a várzea forest, and is home to a large number of fish species which are an essential resource for human consumption.[38] The várzea is also a major source of income through excessive local commercialized fishing.[36][39][40] Várzea consist of muddy river waters containing a vast number and diversity of nutrient-rich species.[41] The abundance of distinct fish species lures the Amazon River dolphin into the várzea areas of high water occurrences during the seasonal flooding.[42]

In addition to attracting predators such as the Amazon river dolphin, these high-water occurrences are an ideal location to draw in the local fisheries.[32]:54–58Human fishing activities directly compete with the dolphins for the same fish species, the tambaqui (Colossoma macropomum) and the pirapitinga (Piaractus brachypomus), resulting in deliberate or unintentional catches of the Amazon river dolphin.[43][44][45][36][46][47][48][49] The local fishermen overfish, and when the Amazon River dolphins remove the commercialized fish from the nets and lines, it damages the equipment and the capture and causes a negative reaction from the local fishermen.[45] [47][48] The Brazilian Institute of Environment and Renewable Natural Resources prohibit fishermen from killing the Amazon river dolphin, yet they are not compensated for the damage to their equipment and the loss of their catch.[49]

Bycatch

During the process of catching the commercialized fish, the Amazon river dolphins get caught in the nets and exhaust themselves until they die, or the local fishermen deliberately kill the dolphins that become entangled in their nets.[38] The carcasses are discarded, consumed, or used as bait to attract a scavenger catfish, the piracatinga (Calophysus macropterus).[38][50] The use of the Amazon river dolphin carcass as bait for the piracatinga dates back from 2000.[50] The increasing consumption demand by the local inhabitants and Colombia for the piracatinga has created a market for distribution of the Amazon river dolphin carcasses to be used as bait throughout these regions.[32]:54–58[49]

For example, of the 15 dolphin carcasses found in the Japurá River in 2010–2011 surveys, 73% of the dolphins were killed for bait, disposed of, or abandoned in entangled gillnets.[38] The data does not fully represent the actual overall number of deaths of the Amazon river dolphins, whether accidental or intentional, because a variety of factors make it extremely complicated to record and medically examine all the carcasses.[38][44][47] Scavenger species feed upon them and the complexity of the river currents makes it nearly impossible to locate all the carcasses.[38] More importantly, the local fishermen do not report these deaths out of fear that legal action will be taken against them,[38] as the Amazon river dolphin and other cetaceans are protected under the Brazilian federal law, prohibiting any takes, harassments, and kills of the species.[51]

In captivity

The only trained Amazon river dolphin in the world at the Acuario de Valencia

A baiji conservation dolphinarium was established at the Institute of Hydrobiology (IHB) in Wuhan in 1992. This was planned as a backup to any other conservation efforts by producing an area completely protected from any threats, and where the baiji could be easily observed. The site includes an indoor and outdoor holding pool, a water filtration system, food storage and preparation facilities, research labs and a small museum. The aim is to also generate income from tourism which can be put towards the baiji plight. The pools are not very large, only kidney shaped tanks with dimensions of 82 feet (25 m) arc 23 feet (7.0 m) width and 11 feet (3.4 m) depth, 33 feet (10 m) diameter, 6.6 feet (2.0 m) deep and 39 feet (12 m) diameter, 11 feet (3.4 m) deep, and are not capable of holding many baijis at one time. Douglas Adams and Mark Carwardine documented their encounters with the endangered animals on their conservation travels for the BBC programme Last Chance to See. The book by the same name, published in 1990, included pictures of a captive specimen, a male named Qi Qi (淇淇) that lived in the Wuhan Institute of Hydrobiology dolphinarium from 1980 to July 14, 2002. Discovered by a fisherman in Dongting Lake, he became the sole resident of the Baiji Dolphinarium (白鱀豚水族馆) beside East Lake. A sexually mature female was captured in late 1995, but died after half a year in 1996 when the Shishou Tian-e-Zhou Baiji Semi-natural Reserve (石首半自然白鱀豚保护区), which had contained only finless porpoises since 1990, was flooded.[52]

The Amazon river dolphin has historically been kept in dolphinariums. Today, only three exist in captivity: one in Acuario de Valencia in Spain, one in Zoologico de Guistochoca in Peru, and one in Duisburg Zoo in Germany. Several hundred were captured between the 1950s and 1970s, and were distributed in dolphinariums throughout the US, Europe, and Japan. Around 100 went to US dolphinariums, and of that, only 20 survived; the last died in Pittsburgh Zoo in 2002.[32]:58–59

In mythology

Ganga on a river dolphin

Old World

In Hindu mythology, the Ganges River Dolphin is associated with Ganga, the deity of the Ganges river. The dolphin is said to be among the creatures which heralded the goddess' descent from the heavens and her mount, the Makara, is sometimes depicted as a dolphin.[53]

In Chinese mythology, the baiji has many origin stories. For example, near the mouth of the Yangtze, the baiji was a princess that had lost her parents and had lived with her step-father, whom she had longed to get away from. The step-father wanted to trade her since she would have been sold for a great sum of money, but as they were crossing the river to get to the trader, a storm rolled in, and they were drenched. The step-father, enraged, tried to take her, but she plunged herself into the river. Before being drowned in the river, she was transformed into a dolphin, and swam away from her abusive step-father, who also fell in and was transformed into a porpoise.[54]

In another story further upstream the Yangtze, the baiji was the daughter of a general who was deported from the city of Wuhan during a war. During his duty, the daughter ran away. Later, the general met a woman who told him how her father was a general, and when he realized that she was his daughter, he threw himself into the river out of shame. The daughter ran after him and also fell into the river. Before they were drowned, the daughter was transformed into a dolphin, and the general a porpoise.[54]

New World

Amazon river dolphins, known by the natives as the boto or encantados, are very prevalent in the mythology of the native South Americans. They are often characterized in their mythology as wielding superior musical ability, their seductiveness and love of sex, often resulting in illegitimate children, and their attraction to parties. Despite the fact that the Encante are said to come from a utopia full of wealth and without pain or death, the encantados crave the pleasures and hardships of human societies.[55]

Transformation into human form is said to be rare, and usually occurs at night. The encantado will often be seen running from a festa, despite protests from the others for it to stay, and can be seen by pursuers as it hurries to the river and reverts to dolphin form. When it is under human form, it wears a hat to hide its blowhole, which does not disappear with the shapeshift.[55]

Besides the ability to shapeshift into human form, encantados frequently wield other magical abilities, such as the power to control storms, enchant humans into doing their will, transform humans into encantados themselves, and inflict illness, insanity, and even death. Shamans often intervene in these situations.[55]

Kidnapping is also a common theme in such folklore. Encantados are said to be fond of abducting humans with whom they fall in love, children born of their illicit love affairs, or just about anyone near the river who can keep them company, and taking them back to the Encante. The fear of this is so great among people who live in the Amazon river area that both children and adults are terrified of going near the water between dusk and dawn, or entering water-bodies alone. Some who supposedly have encountered encantados while out in their canoes have been said to have gone insane, although in fact, the creatures seem to have done little more than follow their boats and nudge them from time to time.[55]

References

  1. 1 2 3 Rice, D. W. (1 January 1998). Marine Mammals of the World: Systematics and Distribution (PDF). Society for Marine Mammalogy. pp. 92–95. ISBN 978-1-891276-03-3. OCLC 40622084.
  2. 1 2 Turvey, S.T.; Pitman, R.L.; Taylor, B.L.; Barlow, J.; Akamatsu, T.; Barrett, L.A.; Zhao, X.; Reeves, R.R.; Stewart, B.S.; Wang, K.; Wei, Z.; Zhang, X.; Pusser, L.T.; Richlen, M.; Brandon, J.R.; Wang, D. (2007). "First human-caused extinction of a cetacean species?". Biology Letters 3 (5): 537–540. doi:10.1098/rsbl.2007.0292. PMC 2391192. PMID 17686754.
  3. Lee, Y.; et al. (2012). "First record of a platanistoid cetacean from the middle Miocene of South Korea". Journal of Vertebrate Paleontology 32 (1): 231–234. doi:10.1080/02724634.2012.626005.
  4. 1 2 Committee on Taxonomy (2012). "List of marine mammal species and subspecies". Society for Marine Mammalogy. Retrieved January 24, 2014.
  5. R.R. Reeves; T.A. Jefferson, L. Karczmarski, K. Laidre, G. O'Corry-Crowe, L. Rojas-Bracho, E.R. Secchi, E. Slooten, B.D. Smith, J.Y. Wang, & K. Zhou (2011). "IUCN 2011. IUCN Red List of Threatened Species, Inia geoffrensis. Version 2011.2.". International Union for Conservation of Nature and Natural Resources.
  6. "List of Marine Mammal Species and Subspecies". Society of Mammalogy. October 2014. Retrieved September 19, 2015.
  7. Dawkins, Richard (2004). The Ancestor's Tale, A Pilgrimage to the Dawn of Life. Houghton Mifflin. pp. 196–203. ISBN 978-0-618-00583-3.
  8. Switek, Brian (9 September 2015). "Fossil "River Dolphin" Lived Out at Sea". Retrieved 2 November 2015.
  9. 1 2 Cassens, I.; Vicario, S.; Waddell, V.G.; Balchowsky, H.; Van Belle, D.; Ding, W.; Fan, C.; Mohan, R.S.; Simões-Lopes, P.C.; Bastida, R.; Meyer, A.; Stanhope, M.J.; Milinkovitch, M.C. (2000). "Independent adaptation to riverine habitats allowed survival of ancient cetacean lineages". Proceedings of the National Academy of Sciences of the United States of America 97 (21): 11343–11347. Bibcode:2000PNAS...9711343C. doi:10.1073/pnas.97.21.11343. PMC 17202. PMID 11027333.
  10. Hamilton, H.; Caballero, S.; Collins, A. G.; Brownell, R. L. (2001). "Evolution of river dolphins". Proceedings of the Royal Society B: Biological Sciences 268 (1466): 549–556. doi:10.1098/rspb.2000.1385. PMC 1088639. PMID 11296868.
  11. 1 2 3 4 Hrbek, T.; da Silva, V.M.F.; Dutra, N.; Gravena, W.; Martin, A.R.; Farias, I.P.; Turvey, S.T. (2014). "A New Species of River Dolphin from Brazil or: How Little Do We Know Our Biodiversity". PLoS ONE 9 (1): e83623. doi:10.1371/journal.pone.0083623. PMC 3898917. PMID 24465386.
  12. Gibbons, Johnny (September 1, 2015). "Fossil Specimen Reveals a New Species of Ancient River Dolphin". Smithsonian Science News. Retrieved September 1, 2015.
  13. Pyenson, N.D.; Vélez-Juarbe, J.; Gutstein, C.S.; Little, H.; Vigil, D.; O'Dea, A. (2015). "Isthminia panamensis, a new fossil inioid (Mammalia, Cetacea) from the Chagres Formation of Panama and the evolution of 'river dolphins' in the Americas". PeerJ 3: e1227. doi:10.7717/peerj.1227. PMC 4562255. PMID 26355720.
  14. Smith, Brian D.; Perrin, William F. (1997). "Distribution, Mortality, Diet and Conservation of Irrawaddy Dolphins (Orcaella Brevirostris) In Lao PDR". Asian Marine Biology 14: 41–48. ISBN 978-962-209-462-8.
  15. Cunha, H.A.; da Silva, V.M.F.; Lailson-Brito, Jr, J.; Santos, M.C.O.; Flores, P.A.C.; Martin, A.R.; Azevedo, A.F.; Fragoso, A.B.L.; Zanelatto, R.C.; Solé-Cava, A.M. (2005). "Riverine and marine ecotypes of Sotalia dolphins are different species". Marine Biology 148 (2): 449–457. doi:10.1007/s00227-005-0078-2.
  16. Secchi, E (2012). "Sotalia fluviatilis. The IUCN Red List of Threatened Species". Retrieved 2 November 2015.
  17. Crespo, Enrique A.; Harris, Guillermo; González, Raúl (1998). "Group size and distribution of the franciscana, Pontoporia blainvellei". Marine Mammal Sciences 14 (4): 845–849. doi:10.1111/j.1748-7692.1998.tb00768.x.
  18. Katherine Ralls; Sarah Mesnick. Sexual Dimorphism (PDF). pp. 1005–1011.
  19. 1 2 3 4 5 6 7 Reidenberg, Joy S. (2007). "Anatomical adaptations of aquatic mammals". The Anatomical Record 290 (6): 507–513. doi:10.1002/ar.20541. PMID 17516440.
  20. Stevens, C. Edward; Hume, Ian D. (1995). Comparative Physiology of the Vertebrate Digestive System. Cambridge University Press. p. 317.
  21. Scholander, Per Fredrik (1940). "Experimental investigations on the respiratory function in diving mammals and birds". Hvalraadets Skrifter 22: 1–131.
  22. Edwards, Holly H.; Schnell, Gary D. (2001). "Body Length, Swimming Speed, Dive Duration, and Coloration of the Dolphin Sotalia fluviatilis (Tucuxi) in Nicaragua" (PDF). Caribbean Journal of Science 37: 271–298.
  23. "Boto (Amazon river dolphin) Inia geoffrensis". American Cetacean Society. 2002. Retrieved September 12, 2015.
  24. Tinker, Spencer. "The Vertebrae of the Cervical Region". Whales of the World. p. 37. ISBN 978-0-935848-47-2.
  25. Nummela, S.; Thewissen, J.G.; Bajpai, S.; Hussain, T.; Kumar, K. (2007). "Sound transmission in archaic and modern whales: anatomical adaptations for underwater hearing.". The Anatomical Record 290 (6): 716–733. doi:10.1002/ar.20528. PMID 17516434.
  26. 1 2 3 4 Thomas, Jeanette A.; Kastelein, Ronald A., eds. (2002). Sensory Abilities of Cetaceans: Laboratory and Field Evidence 196. Springer Science & Business Media. doi:10.1007/978-1-4899-0858-2. ISBN 978-1-4899-0860-5.
  27. Thewissen, J. G. M. (2002). "Hearing". In Perrin, William R.; Wirsig, Bernd; Thewissen, J.G.M. Encyclopedia of Marine Mammals. Academic Press. pp. 570–572. ISBN 978-0-12-551340-1.
  28. Ketten, Darlene R. (1992). "The Marine Mammal Ear: Specializations for Aquatic Audition and Echolocation". In Webster, Douglas B.; Fay, Richard R.; Popper, Arthur N. The Evolutionary Biology of Hearing (PDF). Springer. pp. 725–727. doi:10.1007/978-1-4612-2784-7_44.
  29. Herald, E.S.; Brownell RL, J.; Frye, F.L.; Morris, E.J.; Evans, W.E.; Scott, A.B. (1969). "Blind river dolphin: first side-swimming cetacean". Science 166 (3911): 1408–1410. Bibcode:1969Sci...166.1408H. doi:10.1126/science.166.3911.1408. PMID 5350341.
  30. Stepanek, Laurie (May 19, 1998). "Amazon River Dolphin (Inia geoffrensis)". Texas Marine Mammal Stranding Network. Archived from the original on February 6, 2007. Retrieved November 20, 2013.
  31. 1 2 Mass, Alla M.; Supin, Alexander, Y. A. (May 21, 2007). "Adaptive features of aquatic mammals' eyes". Anatomical Record 290 (6): 701–715. doi:10.1002/ar.20529.
  32. 1 2 3 4 5 6 Klinowska, Margaret; Cooke, Justin (1991). Dolphins, Porpoises, and Whales of the World: the IUCN Red Data Book (PDF).
  33. Braulik, G. T. (2006). "Status assessment of the Indus river dolphin, Platanista minor minor, March–April 2001". Biological Conservation 129 (4): 579–590. doi:10.1016/j.biocon.2005.11.026.
  34. Richard Black (June 27, 2006). "Last Chance for China's Dolphin". Archived from the original on July 6, 2006. Retrieved June 27, 2006.
  35. "Rescue Plan Prepared for Yangtze River Dolphins". July 11, 2002. Retrieved December 18, 2006.
  36. 1 2 3 Silvano, R.A.M.; Ramires, M.; Zuanon, J. (2009). "Effects of fisheries management on fish communities in the floodplain lakes of a Brazilian Amazonian Reserve". Ecology of Freshwater Fish 18: 156–166. doi:10.1111/j.1600-0633.2008.00333.x.
  37. Barletta, M.; Jaureguizar, A.J.; Baigun, C.; Fontoura, N.F.; Agostinho, A.A.; Almeida-Val, V.M.F.; Val, A.L.; Torres, R.A.; Jimenes-Segura, L.F.; Giarrizzo, T.; Fabré, N.N.; Batista, V.S.; Lasso, C.; Taphorn, D.C.; Costa, M.F.; Chaves, P.T.; Vieria, J.P.; Corrêa, M.F.M. "Fish and aquatic habitat conservation in South America: A continental overview with an emphasis on Neotropical systems". Journal of Fish Biology 76: 2118–2176. doi:10.1111/j.1095-8649.2010.02684.x.
  38. 1 2 3 4 5 6 7 Iriarte, V.; Marmontel, M. (2013). "River Dolphin (Inia geoffrensis, Sotalia fluviatilis) Mortality Events Attributed to Artisanal Fisheries in the Western Brazilian Amazon". Aquatic Mammals 39 (2): 116–124. doi:10.1578/am.39.2.2013.116.
  39. Isaac, V.J.; Ruffino, M.L. (2007). "Evaluation of fisheries in Middle Amazon". American Fisheries Society Symposium 49: 587–596.
  40. Neiland, A.E.; Benê, C. (2008). Tropical River Fisheries Valuation:Background papers to a global synthesis. Penang, Malaysia: The World Fish Center. p. 290.
  41. Martin, A.R.; Da Silva, V.M.F.; Rothery, P (2008). "Object carrying as social–sexual display in an aquatic mammal". Animal Behavior, Biology Letters 4: 1243–2145. doi:10.1098/rsbl.2008.0067. PMC 2610054. PMID 18364306.
  42. Arraut, E.M.; Marmontel, M.; Mantovani, J.E.; Novo, E.M.; Macdonald, D.W.; Kenward, R.E. (2009). "The lesser of two evils: seasonal migrations of Amazonian manatees in the Western Amazon". Journal of Zoology 280 (3): 247–256. doi:10.1111/j.1469-7998.2009.00655.x.
  43. Reeves, R.R.; Smith, B.D.; Crespo, E.A.; Notarbartolo di Sciara, G. (2003). Dolphins, whales and porpoises: 2002–2010 conservation action plan for the world's cetaceans. Gland, Switzerland, and Cambridge, UK: International Union for Conservation of Nature/Species Survival Committee. p. 139.
  44. 1 2 Martin, A.R.; Da Silva, V.M.F.; Rothery, P. (2008). "Number, seasonal movements, and residency characteristics of river dolphins in an Amazonian floodplain lake system". Canadian Journal of Zoology 82: 1307–1315. doi:10.1139/z04-109.
  45. 1 2 Loch, Carolina; Marmontel, Miriam; Simões-Lopes, Paulo C. (2009). "Conflicts with fisheries and intentional killing of freshwater dolphins (Cetacea: Odontoceti) in the Western Brazilian Amazon". Biodiversity and Conservation 18 (14): 3979–3988. doi:10.1007/s10531-009-9693-4. ISSN 1572-9710.
  46. Beltrán-Pedreros, S.; Filgueiras-Henriques, L.A. (2010). Biology, evolution and conservation of river dolphins within South America and Asia. New York: Nova Science Publishers Inc. pp. 237–246.
  47. 1 2 3 Crespo, E.A.; Alarcon, D.; Alonso, M.; Bazzalo, M.; Borobia, M.; Cremer, M.; Filla, G.F.; Lodi, L.; Magalhães, F.A.; Marigo, J.; Queiróz, H.L.; Reynolds, J.E. III; Schaeffer, Y.; Dorneles, P.R.; Lailson-Brito, J.; Wetzel, D.L. (2010). "Report on the working group on major threats and conservation". The Latin American Journal of Aquatic Mammals 8 (1-2): 47–56. doi:10.5597/lajam00153.
  48. 1 2 Iriarte, V.; Marmontel, M. (2011). "Report of an encounter with a human intentionally entagled Amazon River dolphin (Inia geoffrensis) calf and its release in Tefé River, Amazonas State, Brazil". Uakari 7 (2): 47–56.
  49. 1 2 3 Alves, L.C.P.S.; Andriolo, A.; Zappes, C.A. (2012). "Conflicts between river dolphins (Cetacea:Odontoceti) and fisheries in the Central Amazon: A path toward tragedy?". Zoologia 29 (5): 420–429. doi:10.1590/s1984-46702012000500005.
  50. 1 2 Estupiñán, G.; Marmontel, M.; Queiroz, H.L.; Roberto e Souza, P.; Valsecchi, J.; da Silva Batista, G.; Barbosa Pereira, S. "A pesca da piracatinga (Calophysus macropterus) na Reserva de Desenvolvimiento Sustentável Mamirauá [The piracatinga fishery (Calophysus macropterus) at Mamirauá Sustainable Development Reserve]." (in Spanish). Brazilian Ministry of Science and Technology. Retrieved July 16, 2014.
  51. Lodi, L.; Barreto, A. (1998). "Legal actions taken in Brazil for the conservation of cetaceans". Journal of International Wildlife Law and Policy 1 (3): 403–411. doi:10.1080/13880299809353910.
  52. Institute of Hydrobiology. "Baiji dolphinarium". Chinese Academy of Sciences. Retrieved September 2, 2015.
  53. Vijay Singh (1994). The River Goddess. London. ISBN 978-1-85103-195-5.
  54. 1 2 Samuel Turvy (2008). "The Goddess of the Yangtze". Witness to Extinction: How we Failed to Save the Yangtze River Dolphin. pp. 3–4. ISBN 978-0-19-954947-4.
  55. 1 2 3 4 Hall, Jamie (2003). "Enchanted Dolphins". Half Human, Half Animal: Tales of Werewolves and Related Creatures. Bloomington, IN. pp. 55–88. ISBN 1-4107-5809-5.

Further reading

This article is issued from Wikipedia - version of the Thursday, January 14, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.