Jump to content

River dolphin

This is a good article. Click here for more information.
From Wikipedia, the free encyclopedia
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

River dolphins
River dolphins are not a taxon, they are an informal grouping of the infraorder Cetacea
Information
Families considered river dolphins
New World range mapNew World river dolphin range map
Old World range mapOld World river dolphin range

River dolphins are a polyphyletic group of fully aquatic mammals that reside exclusively in freshwater or brackish water. They are an informal grouping of dolphins, which itself is a paraphyletic group within the infraorder Cetacea. Extant river dolphins are placed in two superfamilies, Platanistoidea and Inioidea. They comprise the families Platanistidae (the South Asian dolphins), the possibly extinct Lipotidae (Yangtze River dolphin), Iniidae (the Amazonian dolphins) and Pontoporiidae. There are five extant species of river dolphins. River dolphins, alongside other cetaceans, belong to the clade Artiodactyla, with even-toed ungulates, and their closest living relatives the hippopotamuses, from which they diverged about 40 million years ago. Specific types of dolphins can be pink.[1]

River dolphins are relatively small compared to other dolphins, having evolved to survive in warm, shallow water 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 females are larger than the males. 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. Instead, they tend to rely on echolocation when hunting and navigating. 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 widely distributed; 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 2020, there was only one river dolphin in captivity.[2]

Taxonomy and evolution

Classification

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 living family in the superfamily Platanistoidea.[3] 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.[4]

The current classification of river dolphins is as follows:[3][5][6]

Life reconstruction of Arktocara yakataga, an allodelphinid

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.[7][8]

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.[7][9]

Evolution

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.[10] 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.[11]

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.[12][13] Many of the morphological similarities and adaptations to freshwater habitats arose due to convergent evolution; thus, a grouping of all river dolphins is polyphyletic. Amazon river dolphins are actually more closely related to oceanic dolphins than to South Asian river dolphins.[14] 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.[15][16]

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.[12]

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.[17] Some oceanic cetacean populations are known to live semi-permanently in river and estuarine systems, such as the Indo-Pacific bottlenose dolphin group resident in the Swan River of Western Australia which travel as far inland as Belmont.[18]

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.[19] The tucuxi is currently classified as an oceanic dolphin (Delphinidae).[20]

The Franciscana (Pontoporia blainvillei) has shown a converse evolutionary pattern, and has an ancient evolutionary lineage in freshwater, but inhabits estuarine and coastal waters.[21]

Biology

Anatomy

Indus river dolphin skull

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 apart from Amazon river dolphin, with the females being larger than the males.[22][23] 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.[23]

River dolphins have conical teeth, used to catch swift prey such as small river fish.[23] 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.[24] 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.[23][25]

River dolphins have a relatively thin layer of blubber. 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.[23]

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).[26] 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.[27][28] 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.[23]

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.[29] 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.[23][30]: 203–427 [31][32] They are so dependent on echolocation that they can survive even if they are blind.[33] 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.[34]

River dolphins have very small eyes for their size, and do not have a very good sense of sight.[3] 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.[35] They have both rod and cone cells, meaning they can see in both dim and bright light.[35] 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.[30]: 505–519 

Olfactory lobes are absent in river dolphins, suggesting that they have no sense of smell.[30]: 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.[30]: 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 and 1,500 individuals, and genetic diversity is limited.[14] 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.[14] Its probable eventual IUCN status is vulnerable or worse.[14][36]: 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.[36]: 31–32, 37–38 [37]

As China developed economically, pressure on the baiji river dolphin grew significantly.[36]: 41–46  Industrial 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.[38] In the 1950s, the population was estimated at 6,000 animals,[39] 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 and widely accepted sighting was in September 2004, but it has been allegedly seen and photographed by Chinese citizens on four occasions since then.[4][40][41]

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.[42][43] 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.[44] The várzea is also a major source of income through excessive local commercialized fishing.[42][45][46] Várzea consist of muddy river waters containing a vast number and diversity of nutrient-rich species.[47] The abundance of distinct fish species lures the Amazon River dolphin into the várzea areas of high water occurrences during the seasonal flooding.[48]

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.[36]: 54–58  Human 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.[49][50][51][42][52][53][54][55] 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.[51] [53][54] 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.[55]

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.[44] The carcasses are discarded, consumed, or used as bait to attract a scavenger catfish, the piracatinga (Calophysus macropterus).[44][56] The use of the Amazon river dolphin carcass as bait for the piracatinga dates back from 2000.[56] 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.[36]: 54–58 [55]

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.[44] 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.[44][50][53] Scavenger species feed upon them and the complexity of the river currents makes it nearly impossible to locate all the carcasses.[44] More importantly, the local fishermen do not report these deaths out of fear that legal action will be taken against them,[44] as the Amazon river dolphin and other cetaceans are protected under the Brazilian federal law, prohibiting any takes, harassments, and kills of the species.[57]

Conservation

The Global Declaration for River Dolphins was signed by nine countries on 24 October 2023, a date chosen as it is known as the International River Dolphin Day. This pact is intended to promote research and cooperation between countries with river dolphin populations. It is hoped that five further countries will join.[58]

In captivity

One of two trained Amazon river dolphin in the world at the Acuario de Valencia, Venezuela

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.[59]

The Amazon river dolphin has historically been kept in dolphinariums. Today, only three exist in captivity: one in Acuario de Valencia in Venezuela, 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 (named Chuckles) died in Pittsburgh Zoo in 2002.[36]: 58–59 

In mythology

Ganga on a river dolphin

Asia

In Hindu mythology, the Ganges river dolphin is associated with Ganga, the deity of the Ganges river. The dolphin is said to be one of the creatures which heralded the goddess' descent from the heavens, and Ganga's mount, the Makara, is sometimes depicted as a dolphin.[60]

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 stepfather, whom she had longed to get away from. The stepfather wanted to trade her since she would be sold for a great sum of money, but as they were crossing the river to get to the trader, a storm rolled in. The enraged stepfather tried to take her, but she plunged herself into the river, was transformed into a dolphin before she drowned, and swam away from her abusive stepfather, who also fell in and was transformed into a porpoise.[61]

In another story, the baiji was the daughter of a general deported from the city of Wuhan during a war who ran away while her father was in duty. Later, the general met a woman who told him how her father was a general. When he realized that she was his daughter, he threw himself into the river out of shame, and his daughter ran after him and also fell into the river. Before they were drowned, the daughter was transformed into a dolphin and the general into a porpoise.[61]

South America

Amazon river dolphins, known by the natives as the boto, encantados or toninhas, are very prevalent in the mythology of the native South Americans. They are often characterized in mythology with superior musical ability, seductiveness and love of sex that often results in illegitimate children, and 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.[62]

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.[62]

Besides the ability to shapeshift into human form, encantados frequently wield other magical abilities, such as controlling storms, hypnotizing humans into doing their will, transforming humans into encantados, and inflicting illness, insanity, and even death. Shamans often intervene in these situations.[62]

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 near the Amazon River that both children and adults are terrified of going near the water between dusk and dawn, or entering water alone. Some who supposedly have encountered encantados while out in their canoes have been said to have gone insane, but the creatures seem to have done little more than follow their boats and nudge them from time to time.[62]

References

  1. ^ "Amazon River Dolphin (Pink Dolphins) | Species | WWF". World Wildlife Fund. Retrieved 2021-04-21.
  2. ^ "The last river dolphin". Whale & Dolphin Conservation UK. 2020-12-22. Retrieved 2023-09-15.
  3. ^ a b c 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.
  4. ^ a b 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.
  5. ^ Rice, Dale W. (2009). "Classification (Overall)". Encyclopedia of Marine Mammals (2nd ed.). Academic Press. pp. 234–238. doi:10.1016/B978-0-12-373553-9.00058-4. ISBN 9780123735539.
  6. ^ 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. Bibcode:2012JVPal..32..231L. doi:10.1080/02724634.2012.626005. S2CID 129560068.
  7. ^ a b Committee on Taxonomy (2012). "List of marine mammal species and subspecies". Society for Marine Mammalogy. Archived from the original on January 6, 2015. Retrieved January 24, 2014.
  8. ^ Reeves, R.R., Jefferson, T.A., Karczmarski, L., Laidre, K., O’Corry-Crowe, G., Rojas-Bracho, L., Secchi, E.R., Slooten, E., Smith, B.D., Wang, J.Y. & Zhou, K. (2011). Inia geoffrensis. The IUCN Red List of Threatened Species doi:10.2305/IUCN.UK.2011-1.RLTS.T10831A3220342.en
  9. ^ "List of Marine Mammal Species and Subspecies". Society of Mammalogy. October 2014. Archived from the original on January 6, 2015. Retrieved September 19, 2015. {{cite journal}}: Cite journal requires |journal= (help)
  10. ^ 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.
  11. ^ Switek, Brian (9 September 2015). "Fossil "River Dolphin" Lived Out at Sea". Archived from the original on September 10, 2015. Retrieved 2 November 2015.
  12. ^ a b 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.
  13. ^ 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.
  14. ^ a b c d 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. Bibcode:2014PLoSO...983623H. doi:10.1371/journal.pone.0083623. PMC 3898917. PMID 24465386.
  15. ^ Gibbons, Johnny (September 1, 2015). "Fossil Specimen Reveals a New Species of Ancient River Dolphin". Smithsonian Science News. Retrieved September 1, 2015.
  16. ^ 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.
  17. ^ Smith, Brian D.; Perrin, William F. (1997). Distribution, Mortality, Diet and Conservation of Irrawaddy Dolphins (Orcaella Brevirostris) In Lao PDR. Vol. 14. pp. 41–48. ISBN 978-962-209-462-8. {{cite book}}: |journal= ignored (help)
  18. ^ "Dolphins on the Swan River - WA Achievers".
  19. ^ Cunha, H.A.; da Silva, V.M.F.; Lailson-Brito, J. Jr; 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. Bibcode:2005MarBi.148..449C. doi:10.1007/s00227-005-0078-2. S2CID 49359327.
  20. ^ Secchi, E. (2012). Sotalia fluviatilis. The IUCN Red List of Threatened Species doi:10.2305/IUCN.UK.2012.RLTS.T190871A17583369.en
  21. ^ Crespo, Enrique A.; Harris, Guillermo; González, Raúl (1998). "Group size and distribution of the franciscana, Pontoporia blainvellei". Marine Mammal Science. 14 (4): 845–849. doi:10.1111/j.1748-7692.1998.tb00768.x.
  22. ^ Ralls, Katherine; Mesnick, Sarah. Sexual Dimorphism (PDF). pp. 1005–1011. Archived from the original (PDF) on 2019-07-25. Retrieved 2015-09-12.
  23. ^ a b c d e f g Reidenberg, Joy S. (2007). "Anatomical adaptations of aquatic mammals". The Anatomical Record. 290 (6): 507–513. doi:10.1002/ar.20541. PMID 17516440. S2CID 42133705.
  24. ^ Stevens, C. Edward; Hume, Ian D. (1995). Comparative Physiology of the Vertebrate Digestive System. Cambridge University Press. p. 317. ISBN 978-0521617147.
  25. ^ Scholander, Per Fredrik (1940). "Experimental investigations on the respiratory function in diving mammals and birds". Hvalraadets Skrifter. 22: 1–131.
  26. ^ 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.
  27. ^ "Boto (Amazon river dolphin) Inia geoffrensis". American Cetacean Society. 2002. Retrieved September 12, 2015.
  28. ^ Tinker, Spencer (1988-01-01). "The Vertebrae of the Cervical Region". Whales of the World. Brill Archive. p. 37. ISBN 978-0-935848-47-2.
  29. ^ Nummela, S.; Thewissen, J.G.; Bajpai, S.; Hussain, T.; Kumar, K. (2007). "Sound transmission in archaic and modern whales: anatomical adaptations for underwater hearing" (PDF). The Anatomical Record. 290 (6): 716–733. doi:10.1002/ar.20528. PMID 17516434. S2CID 12140889.
  30. ^ a b c d Thomas, Jeanette A.; Kastelein, Ronald A., eds. (2002). Sensory Abilities of Cetaceans: Laboratory and Field Evidence. Vol. 196. Springer Science & Business Media. doi:10.1007/978-1-4899-0858-2. ISBN 978-1-4899-0860-5. S2CID 32801659.
  31. ^ Thewissen, J. G. M. (2002). "Hearing". In Perrin, William R.; Wirsig, Bernd; Thewissen, J.G.M. (eds.). Encyclopedia of Marine Mammals. Academic Press. pp. 570–572. ISBN 978-0-12-551340-1.
  32. ^ Ketten, Darlene R. (1992). "The Marine Mammal Ear: Specializations for Aquatic Audition and Echolocation". In Webster, Douglas B.; Fay, Richard R.; Popper, Arthur N. (eds.). The Evolutionary Biology of Hearing. Springer. pp. 725–727. doi:10.1007/978-1-4612-2784-7_44. ISBN 978-1-4612-7668-5.
  33. ^ 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. S2CID 5670792.
  34. ^ 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.
  35. ^ a b 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. PMID 17516421. S2CID 39925190.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  36. ^ a b c d e f Klinowska, Margaret; Cooke, Justin (1991). Dolphins, Porpoises, and Whales of the World: the IUCN Red Data Book (PDF).
  37. ^ 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.
  38. ^ Black, Richard (June 27, 2006). "Last Chance for China's Dolphin". Archived from the original on July 6, 2006. Retrieved June 27, 2006.
  39. ^ "Rescue Plan Prepared for Yangtze River Dolphins". July 11, 2002. Retrieved December 18, 2006.
  40. ^ "中华白鱀豚功能性灭绝十年后疑似重现长江,科考队称拍到两头_绿政公署_澎湃新闻-The Paper". m.thepaper.cn. Retrieved 2024-11-13.
  41. ^ "The Search for the Baiji". The World of Chinese. Retrieved 2024-11-13.
  42. ^ a b c 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 (1): 156–166. Bibcode:2009EcoFF..18..156S. doi:10.1111/j.1600-0633.2008.00333.x.
  43. ^ 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. (2010). "Fish and aquatic habitat conservation in South America: A continental overview with an emphasis on Neotropical systems". Journal of Fish Biology. 76 (9): 2118–2176. Bibcode:2010JFBio..76.2118B. doi:10.1111/j.1095-8649.2010.02684.x. PMID 20557657.
  44. ^ a b c d e f g 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.
  45. ^ Isaac, V.J.; Ruffino, M.L. (2007). "Evaluation of fisheries in Middle Amazon". American Fisheries Society Symposium. 49: 587–596.
  46. ^ Neiland, A.E.; Benê, C. (2008). Tropical River Fisheries Valuation:Background papers to a global synthesis. Penang, Malaysia: The World Fish Center. p. 290.
  47. ^ Martin, A.R.; Da Silva, V.M.F.; Rothery, P (2008). "Object carrying as social–sexual display in an aquatic mammal". Biology Letters. 4 (3): 1243–2145. doi:10.1098/rsbl.2008.0067. PMC 2610054. PMID 18364306.
  48. ^ 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.
  49. ^ 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.
  50. ^ a b 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 (8): 1307–1315. doi:10.1139/z04-109.
  51. ^ a b 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. Bibcode:2009BiCon..18.3979L. doi:10.1007/s10531-009-9693-4. ISSN 1572-9710. S2CID 20873255.
  52. ^ 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.
  53. ^ a b c 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. hdl:11336/98669.
  54. ^ a b 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.
  55. ^ a b c 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.
  56. ^ a b 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. Archived from the original on July 28, 2014. Retrieved July 16, 2014.
  57. ^ 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.
  58. ^ Astrid Arellano (15 January 2024). "Nine countries sign global pact to protect endangered river dolphins". Mongabay. Retrieved 20 January 2024.
  59. ^ Institute of Hydrobiology. "Baiji dolphinarium". Chinese Academy of Sciences. Archived from the original on February 3, 2022. Retrieved September 2, 2015.
  60. ^ Singh, Vijay (1994). The River Goddess. London. ISBN 978-1-85103-195-5.{{cite book}}: CS1 maint: location missing publisher (link)
  61. ^ a b Samuel Turvy (2008). "The Goddess of the Yangtze". Witness to Extinction: How we Failed to Save the Yangtze River Dolphin. Oxford University Press. pp. 3–4. ISBN 978-0-19-954947-4. ASIN 0199549486.
  62. ^ a b c d Hall, Jamie (2003). "Enchanted Dolphins". Half Human, Half Animal: Tales of Werewolves and Related Creatures. Bloomington, IN. pp. 55–88. ISBN 978-1-4107-5809-5.{{cite book}}: CS1 maint: location missing publisher (link)

Further reading

  • Reeves, Randall R. et al. (2002). National Audubon Society Guide to Marine Mammals of the World. Alfred A. Knopf. 527 pp.