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Overview

Brief Summary

Biology

Little is known of the reproductive habits of the tucuxi dolphin. The freshwater subspecies calves during the low water period of October and November (2), after an 11 to 12 month gestation. It is thought to be polyandrous (where each female has more than one male partner), and aggression between males is seen during courtship (5). The seasonal fluctuation in river water levels has a great influence on the freshwater subspecies. It enters lakes during high water but leaves as the waters begin to fall to avoid being trapped (2). A shy dolphin, the tucuxi tends to be most active during the early morning and late afternoon, but is usually a slow swimmer that jumps infrequently (5). It dives for around 30 seconds (4), and uses echolocation to communicate as well as to catch fish and shrimp (5). Group size varies, but can be up to 20 in freshwater or 50 in the marine subspecies (3).
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Description

The tucuxi dolphin (pronounced 'too-koo-shee') quite closely resembles the bottlenose dolphin, but smaller. It is blue to light grey on the back, and fades to white or whitish-pink on the belly. There is a dark bar between the mouth and the flipper. The beak is slender and long, and the dorsal fin is triangular and slightly hooked at the tip (2). Both the beak and the dorsal fin may be tipped with white (5). Some marine populations have yellow-orange sides with a bright patch on the dorsal fin (5).
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Sotalia fluviatilis

Habitat dolpin mostly in both fresh and saltwater(sea), but for species Sotalia fluviatilis they are live in saltwater and near to the surface and we can found around the world it can be found nearly everywhere including the Indian ,Atlantic, & Pacific Oceans, the Mediterrean, Red & Black Seas. Dolpin always make a group ,that is these lifestyle and this group so important becouse these need each other example for looking a food ,hunting and to protect these self from predators. These will make same noise for protect self, guide they child also group. It is the way they to communication. The sound of dolphins can be grouped into three types, that is (1) click for echolocation, (2) bursering described as a screech or bark, (3) whistle usually used for communication. Dolpin also life at depths greater than 200 meters but they will depend to the noise than a light.Dolpin life is more rely to sound rather than sight and hearing. Dolphins cannot breathe under water. They breathe out of their blowhole. This is why we can’t put anything in their blowhole, because this is their route to breathe and make sounds. But they can hold their breath for amazing amounts of time seven minutes. So they do need to come up for a breath . That make doplin including in active swimmer, because they speeds of swiming is 60 km / h or 37 mph . They always swim like activity jumps to the air with the head first and fell back into the water.Some reviewer called this activity is breaching. Dolpin also do not sleep well under water for a long time because they will could drown. Therefore, when they sleep only was half asleep a few moments in a day. They also do migrate if the water gets so cold the temperature in minimum stage. Also they may migrate if the fish supply and feeding habits change and looking for food. They can even travel hundreds of miles just to follow their food supply. Some like cold and deeper water than others. But if there is enough food available then they may just stick to a local area.

  • Shane, H. 1990. Behaviour and Ecology of The Bottlenose Dolphin at Sanibel
  • Island, Florida. In: S. Leatherwood, S. dan R.R.Reeves. The Bottlenose
  • Dolphin. Academic Press, Inc.San Diego, California, United States of
  • America:235-245.
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Distribution

Range Description

Tucuxis are found in the Amazon drainage as far inland as southern Peru, eastern Ecuador, and southeastern Colombia. They occur in the main tributaries of the Amazon/Solimões River basin and they cross international boundaries in areas such as Leticia, between Brazil and Colombia. The species does not occur in the Beni/Mamoré river basin in Bolivia nor in the upper Rio Negro. Its putative presence in the Orinoco is controversial because of a stretch of rapids and waterfalls that are suspected to block the species movements to this area (Flores and da Silva 2009). During the flood season, Tucuxis may move into smaller tributaries, but apparently they do not move into the inundated forest to feed (as botos, Inia geoffrensis, often do), staying mainly in the main river channels, tributaries and lakes (da Silva and Best 1996). Tucuxis are largely sympatric with the Boto in the Amazon and Orinoco systems but generally do not interact with that species.

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Geographic Range

Tucuxis, also known as gray dolphins and Guianian River dolphins, are neotropical dolphins that live exclusively in the Amazon and Orinoco basins and are thought to be endemic to this region of South America. The closest living relatives of Tucuxis are Costeros, dolphins that live in the shallow waters along the Atlantic Coast of South America. However, Tucuxis are sympatric with Amazon River dolphins of the family Iniidae.

Biogeographic Regions: neotropical (Native )

  • Beneditto, A., R. Ramos. 2004. Biology of the marine tucuxi dolphin (Sotalia £uviatilis) in south-eastern Brazil. Journal of the Marine Biological Association of the United Kingdom, Vol. 84, no. 6,: 1245-1250..
  • Caballero, S., F. Trujillo, J. Vianna, H. Barrios-Garrido, M. Montiel, S. Beltran-Pedreros, M. Marmontel, M. Santos, M. Rossi-Santos, F. Santos, C. Baker. 2007. Taxonomic status of the genus sotalia: Species level ranking for "Tucuxi" (Sotalia fluviatilis) and "Costero" (Sotalia guianensis) dolphins. Marine Mammal Science, 23/2: 358-386.
  • Cunha, H., V. da Silva, J. Lailson-Brito, M. Santos, P. Flores, A. Martin, A. Azevedo, A. Fragoso, R. Zanelatto, A. Sole-Cava. 2005. Riverine and marine ecotypes of Sotalia dolphins are different species. Marine Biology, 148/2: 449-457.
  • Ding, W., B. Wursig, S. Leatherwood. 2001. Whistles of boto, Inia geoffrensis, and tucuxi, Sotalia fluviatilis. Acoustical Society of America, 109/1: 407-411.
  • Flores, P., V. da Silva. 2009. Tucuxi and Guiana Dolphin. Pp. 1188-1192 in J Thewissen, ed. Encyclopedia of Marine Mammals, Vol. 1, 2nd Edition. London: Academic.
  • Martin, A., V. da Silva, D. Salmon. 2004. Riverine Habitat Preferences of Botos (Inia geoffrensis) and Tucuxis (Sotalia fluviatilis) in the Central Amazon. Marine Mammal Science, Vol. 20, no. 2: 189-200.
  • Nowak, R. 1999. Tucuxi, or River Dolphin. Pp. 920-923 in Mammals of the World, Vol. 2, 6th Edition. Baltimore and London: The Johns Hopkins University Press.
  • Oliveira, A. 2005. Group characteristics of marine tucuxis (Sotalia fluviatilis) (Cetacea: Delphinidae) in Guanabara Bay, south-eastern Brazil. Journal of the Marine Biological Association of the United Kingdom, 85/1: 209-212.
  • Secchi, E. 2010. "Sotalia fluviatilis" (On-line). Accessed November 12, 2010 at http://www.iucnredlist.org/apps/redlist/details/190871/0.
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Amazon River
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Range

Occurring in the river systems of the Amazon and the Orinoco, as well as along the coasts from Brazil to Nicaragua, the tucuxi dolphin is split into two subspecies. The freshwater subspecies, Sotalia fluviatilis fluviatilis, inhabits only fresh water and is found as much as 250 km up the Orinoco River system and as much as 2,500 km up the Amazon River system. The marine subspecies, Sotalia fluviatilis guianensis, is found in the coastal estuaries and bays of the east coast of South America as far south as the Brazilian city of Florianópolis (2).
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Physical Description

Morphology

Physical Description

Sotalia fluviatilis and Sotalia guianensis are very similar in appearance and were once classified as a single species. However, phylogenetic evidence indicates that they diverged approximately 1.5 to 2 million years ago during the Pliocene or early Pleistocene. Despite their many similarities, three major differences help distinguish between these 2 species. First, S. fluviatilis largely prefers fresh water habitat, whereas S. guianensis prefers saline coastal habitat. Second S. fluviatilis is much smaller in size than S. guianensis. Finally, the haplotype and nucleotide sequences of S. fluviatilis are as diversified from S. guianensis as they are from other delphinids. In general, S. fluviatilis is smaller and has a shorter beak than most other members of the family Delphinidae. It ranges from blue to pearl-grey along the dorsal surface and from white to pale-pink along the ventral surface. Most individuals have a white tipped beak. The dorsal fin has a prominent triangular shape that sometimes hooks toward the caudal fin. Adults have between 28 and 35 teeth. Sotalia fluviatilis is not sexually dimorphic and ranges from 86 to 206 cm long and weighs 55 kg on average.

Average mass: 55 kg.

Range length: 86 to 206 cm.

Average length: 152 cm.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: sexes alike

Average mass: 46666.7 g.

  • Emmons, L. 1990. Neotropical Rainforest Mammals: A Field Guide. Chicago and London: The University of Chicago Press.
  • da Silva, V., A. Carter, C. Ambrosio, A. Carvalho, M. Bonatelli, M. Lima, M. Miglino. 2007. Placentation in dolphins from the Amazon River Basin: the Boto, Inia geoffrensis, and the Tucuxi, Sotalia fluviatilis. Reproductive Biology and Endocrinology, 5: 26-26.
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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology

Tucuxis inhabit all three types of water of the Amazon basin: white water, clear water, and black water. Therefore, physical factors such as visibility and acidity appear not to affect their distribution directly. They seem to prefer the main channels of rivers and larger lakes where access is not limited by a narrow or shallow channel, while rapids and fast-moving turbulent water are avoided. Tucuxis also generally do not enter the flooded forest. They are mostly found within 50 m of the edges of rivers and channels (Martin et al. 2004). Similarly to the sympatric boto, the tucuxi shows a distinct preference for junctions of rivers and channels (da Silva and Best 1996, Leatherwood et al. 2000, Martin et al. 2004). The most preferred habitat is where a sediment-rich whitewater channel meets the low pH- carrying black water. The resultant mixing produces productive and obviously attractive conditions for dolphins (Martin et al. 2004). The large seasonal fluctuation in river levels (10m) influences the distribution of tucuxis. They enter lake systems during periods of high water but leave these environments as the waters recede, thus avoiding entrapment. In the Peruvian Amazon, tucuxis were not found in waters <3m depth in rivers or <1.8 m depth in lakes.

Individuals may occur in the same area year-round. Two tagged individuals in the Amazon were found within 5 km of the tagging site up to 1 year later (da Silva and Best 1994). A long-term photo-identification study revealed a maximum range for individuals of 130 km in Peru's Pacaya-Samiria Reserve (McGuire and Henningsen 2007). This relatively small range is probably due to limiting features such as small channels and seasonally shallow waters. According to McGuire (2002), encounter rates were highest in confluences, intermediate in lakes, and lowest in rivers and did not differ among seasons in the latter two. During the dry season, tucuxis persisted longer in the confluences and occurred in higher densities than in any rainy or intermediate season; the reverse pattern was observed during high water.

S. fluviatilis occurs most often in groups of one to six individuals. Groups of more than nine animals are rarely observed (da Silva and Best 1994, Faustino and da Silva 2006). The composition of groups is unknown. Vidal et al. (1997) reported overall mean group size of 3.9 in the upper Amazon. Tucuxis were most frequently seen as singles or pairs in rivers and lakes of Peru's Pacaya-Samiria Reserve; seasonal differences in group size were non-significant (McGuire 2002).

Information on reproduction is sparse. Males attain sexual maturity at approximately 140cm and females at between 132 and 137cm (da Silva and Best 1996). In Brazil, gestation lasts about 11 months and calves are about 80 cm long at birth, which occurs primarily from September to November during the low-water period (da Silva and Best 1996, Flores and da Silva 2009). Neonate tucuxi were observed in all seasons in the Peruvian Amazon, with a slight peak in encounter rates during high water (McGuire and Aliaga 2007).

At least 28 species of mostly small schooling fish belonging to 11 families are preyed upon by tucuxis in the Amazon region. The characoid family Curimatidae was represented in 52%, Sciaenidae in 39% and siluriforms in 54% of stomachs analysed (n = 29) (da Silva and Best 1994). During the dry season, fish concentrate in the main water bodies and thus are more vulnerable to predation. During the flood season, many species enter the floodplain and are largely out of reach of tucuxis.


Systems
  • Freshwater
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Tucuxis are found throughout the Amazon and Orinoco River basins and are commonly found near low current confluences and river junctions where food is abundant and less energy has to be expended during foraging bouts. They avoid mud banks and flooded forest areas. The mouth of the Amazon River occurs at its junction with the Atlantic ocean, thus making the first 2 km of the river relatively saline. Although some Tucuxi can be found within this area, they prefer the freshwater habitat found further inland.

Habitat Regions: tropical ; freshwater

Aquatic Biomes: rivers and streams; brackish water

Other Habitat Features: estuarine

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In freshwater in Amazon and Orinoco drainage basins.
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The freshwater subspecies inhabits rivers and lakes, but is not found in flooded forests and avoids rapids, whereas the marine subspecies inhabits shallow, protected estuaries and bays (2).
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Trophic Strategy

Food Habits

Tecuxis are carnivorous, and primary prey includes marine ray-finned fishes, along with squids and octopuses. Confluence areas result in favorable pH levels for plankton growth, which attracts many species of ray-finned fish. As a result, Tucuxis are often seen travelling to confluences, likely in search of prey.

Animal Foods: fish; mollusks

Primary Diet: carnivore (Piscivore , Molluscivore )

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Associations

Ecosystem Roles

Although barnacles are commonly found Tucuxis, they are not considered parasitic, as they have no known negative impact on their host. Limited information exists regarding parasites of Tucuxis; however, stomach flukes and two species of nematode (Anisakis typica and Halocercus brasiliensis) are known to infect the gastrointestinal tissues of this species at various stages throughout their complex life cycle.

Commensal/Parasitic Species:

  • Kane, E., P. Olson, T. Gerrodette, P. Fiedler. 2008. Prevalence of the commensal barnacle Xenobalanus globicipitis on cetacean species in the eastern tropical Pacific Ocean, and a review of global occurrence. Fishery Bulletin, 106/4: 395-404.
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Predation

Other than illegal hunting by humans, Tucuxis have no known predators.

Known Predators:

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Life History and Behavior

Behavior

Communication and Perception

Like most dolphins, Tucuxis use a variety of whistles and clicks to communicate with conspecifics. Among delphinids, evidence suggests that species' size has a linear effect on whistle pitch, with smaller species having higher pitched whistles and larger species having lower pitched whistles. Tucuxis align with this relationship, and as one of the smallest extant dolphin species, they are known to have some of the highest pitched whistles when compared to other dolphins (e.g., 16% of whistles exceed 24Hz). Whistle frequency tends to ascend rather than descend during a single whistle. Whistling increases while foraging, and is thought to attract conspecifics to where food is abundant; suggesting a co-operative rather than competitive attitude between conspecifics. Like other delphinids, Tucuxis use echolocation to help them find prey.

Tecuxis use their vision to perceive the local environment, and despite living in a freshwater environment, have a number of ocular features that are similar to those of many marine dolphins. Tucuxis have two high density ganglion areas, a feature which is common among delphinids and helps them process visual information more efficiently than Amazon River dolphins, which have only one. Being originally adapted for life in a saline environment, however, may negatively affect their ability to see objects in freshwater at high resolution. Evidence suggests that although their clarity of vision is less than that of true river dolphins, it is better than that of marine dolphins. What they lack in eye sight, however, they make up for in their ability to echolocate prey and potential predators.

Communication Channels: acoustic

Perception Channels: visual ; echolocation

  • Azevedo, A., M. Van Sluys. 2005. Whistles of tucuxi dolphins (Sotalia fluviatilis) in Brazil: Comparisons among populations. Acoustical Society of America, 117/3: 1456–1464.
  • Mass, A., A. Supin. 1999. Retinal topography and visual acuity in the riverine tucuxi (Sotalia fluviatilis). Marine Mammal Science: 351-365.
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Life Expectancy

Lifespan/Longevity

Evidence suggests that wild Tucuxis can live for up to 35 years. There is no information available indicating the average lifespan of captive individuals. They are susceptible to capture stress and often tangle and suffocate themselves within netting. In addition, Tucuxi do not respond well to extended periods of transportation.

Average lifespan

Status: wild:
35 years.

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Lifespan, longevity, and ageing

Observations: Little is known about the longevity of these animals, but one wild born specimen was still living in captivity at about 31-32 years of age (Richard Weigl 2005).
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Reproduction

There is no information available regarding the mating system of Tucuxis.

Tucuxis breed during late summer and early fall. Gestation ranges from 10 to 11.6 months and results in one calf, which is born during the fall low-water season. Newborn calves range in size from 71 to 106 cm in length. Both sexes become sexually mature by six years of age, at which point males are around 180 cm long and females are around 160 cm long. Despite their differences in length at reproductive maturity, fully grown males and females are usually equal in length and weight.

Breeding season: Tucuxis breed from August to October.

Average number of offspring: 1.

Range gestation period: 10 to 11.6 months.

Average age at sexual or reproductive maturity (female): 6 years.

Average age at sexual or reproductive maturity (male): 6 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); viviparous

Average number of offspring: 1.

Little is known of parental care in Tucuxis; however, mothers are known to whistle at their calves once they have found food. As mammal, mothers likely nurse their young until weaning is complete.

Parental Investment: female parental care ; pre-hatching/birth (Provisioning: Female, Protecting: Female); pre-weaning/fledging (Provisioning: Female, Protecting: Female)

  • Beneditto, A., R. Ramos. 2004. Biology of the marine tucuxi dolphin (Sotalia £uviatilis) in south-eastern Brazil. Journal of the Marine Biological Association of the United Kingdom, Vol. 84, no. 6,: 1245-1250..
  • Flores, P., V. da Silva. 2009. Tucuxi and Guiana Dolphin. Pp. 1188-1192 in J Thewissen, ed. Encyclopedia of Marine Mammals, Vol. 1, 2nd Edition. London: Academic.
  • Pivari, D., S. Rosso. 2005. Whistles of small groups of Sotalia fluviatilis during foraging behavioural in southeastern Brazil. Acoustical Society of America, 118/4: 2725-2731.
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Molecular Biology and Genetics

Molecular Biology

Statistics of barcoding coverage: Sotalia fluviatilis

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 0
Specimens with Barcodes: 3
Species With Barcodes: 1
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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
DD
Data Deficient

Red List Criteria

Version
3.1

Year Assessed
2010

Assessor/s
Secchi, E.

Reviewer/s
Reeves, R. & Perrin , W.

Contributor/s

Justification

The split of Sotalia into two species has conservation relevance. The Tucuxi can be considered the world's only exclusively freshwater delphinid. This endemism jeopardizes its persistence because its restricted habitat is shared with increasing human populations. Tucuxis are vulnerable to threats such as incidental mortality in fisheries, habitat deterioration and fragmentation of populations by dam construction (Reeves at al. 2003). No formal assessment to evaluate the risks of population decline has been performed. Such assessment will require a better understanding of population structure so that population-specific abundance, non-natural mortality rates and other relevant parameters can be estimated and considered. Due to a lack of good data on these parameters, Sotalia fluviatilis is listed as Data Deficient.

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Tucuxis are classified as "data deficient" on the IUCN Red List of Threatened Species. Currently, population trends are unknown and thus potential conservation and management needs cannot be determined. They are the only species of fresh-water delphinid currently known. Although there has never been a commercial fishery for this species, a significant number of deaths occur due to by-catch and incidental mortality in fishing gear. Other potentially important threats include damming, overfishing of prey, boat strikes, chemical pollution and noise pollution. Without further research on the demographics of this species throughout its geographic range, the significance of these threats cannot be established and potential conservation and management actions cannot be prioritized.

US Federal List: no special status

CITES: appendix i

State of Michigan List: no special status

IUCN Red List of Threatened Species: data deficient

  • Trujillo Gonzalez, F. 1994. The use of photoidentification to study the Amazon river dolphin, Inia geoffrensis, in the Colombian Amazon. Marine Mammal Science, 10/3: 348-353.
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Status

The tucuxi dolphin is classified as Data Deficient on the IUCN Red List 2004 (1), and is listed on Appendix I of CITES (5). It is also listed on Appendix II of the Convention on Migratory Species (2).
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Population

Population
To date, there is no information on the population structure of S. fluviatilis. The only data available suggest that the species has moderate to high genetic diversity, since 12 individuals from the same location in the central Brazilian Amazon had five different control region haplotypes (Cunha et al. 2005), and 21 dolphins from the Peruvian, Colombian and Brazilian Amazon had 13 haplotypes (combining the control region and ND2, Caballero et al. 2007). Microsatellite variation is also larger in S. fluviatilis (H = 0.531) than in S. guianensis (H = 0.364; Cunha and Watts 2007). The reason for a higher level of genetic variation in S. fluviatilis, in spite of its probably smaller population size, remains to be determined. There are no estimates of the total population size for S. fluviatilis, though it appears to be relatively abundant throughout most of its range (Flores and da Silva 2009). Local estimates of relative abundance exist for some areas. In the Amazon drainage, an average density (encounter rate) of approximately 1.1 dolphins/km of river was estimated between Manaus and Tefé in the Solimões River (Magnusson et al. 1980). Four boat surveys of about 1,525 km each, from Manaus to Letícia, resulted in a mean estimate of 768 (± 104.7 SD) dolphins per trip or 1.02 individuals/km² (da Silva and Best 1994). More recently, mean density along the margins of main rivers in the central Amazon, Brazil (1,320 km of strip survey) was estimated at 3.2 individuals/km². About 54% of the individuals were found within 50 m of the edge of rivers and channels (Martin et al. 2004). Faustino and da Silva (2006) recorded on average 24 Tucuxis/km in the Mamirauá System, Central Amazon. Higher densities were found in deeper channels with high turbulence and productivity.

About 350 Tucuxis were estimated to inhabit the Samiria River system in Peru (Leatherwood 1996). Recent studies indicate that encounter rates in this area were within the range for these dolphins elsewhere in South America and that population numbers were stable over 10 years between 1991 and 2000 (McGuire 2002). Mean encounter rates in the Peruvian Amazon were 0.01-080 individuals/km in rivers and 0.05-2.17 individuals/km² in lakes (28 surveys over a four-year time period; McGuire 2002). The species is reportedly common in Colombia in the Loretoyacu River, in the Tarapoto River and in the El Correo Lake system (da Silva and Best 1994). Vidal et al. (1997) estimated that in 1993 there were 409 Tucuxis (CV=13%) along 120 km of the Amazon River bordering Colombia, Peru, and Brazil. Density (dolphins/km²) was highest in lakes (8.6), followed by areas along main banks (2.8) and around islands (2.0). Those estimates of density or abundance in small portions of the range are of limited use for assessment of the conservation status of the species as a whole.

Population Trend
Unknown
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Threats

Major Threats
There are no records of past or recent commercial fisheries for Sotalia spp. (IWC 2001). River dolphins in the Amazon region are threatened primarily by incidental mortality in fishing gear (IWC 2001). S. fluviatilis consumes 14 of the 30 species of commercially exploited fish in the Amazon, and thus incidental captures during fishing are frequent (da Silva and Best 1994, 1996; Martin et al. 2004). In one study in the central Amazon of Brazil, 74% of 34 tucuxis examined had been killed in gill nets and 15% in seine nets (da Silva and Best 1985). By-catch in fishing gear, caused by the proliferation of gill nets, and some evidence of poisoning by commercial fishermen, seem to be the main conservation threats to tucuxis in Peru (Reeves et al. 1999).

Other potentially important threats are oil spills, boat strikes, chemical and noise pollution, overfishing of prey, and damming of rivers for hydroelectric projects (da Silva and Best 1994, Denkinger 2001, McGuire 2002). Dams can interrupt gene flow and create isolated groups of dolphins with reduced genetic variability and lowered demographic resilience. The use of pesticides banned in many countries continues to be common in some parts of South America (PNUMA 2002). Mercury is used to refine fluvial gold and then, like the pesticides, enters aquatic food webs. Dams, in addition to fragmenting dolphin populations, can have serious effects on migratory fish populations on which tucuxis feed (such as some siluriform fishes) (da Silva and Best 1994). The increased use of outboard engines and illegal fishing with explosives are also sources of concern in parts of these dolphins' range (e.g. Utreras et al. 2001, Zapata-Rios and Utreras 2004).

Although freshwater dolphins have been protected by superstitions in parts of Amazonia (Leatherwood and Reeves 1997), in Colombia and Brazil there was and may still be a small market for the eyes, teeth and reproductive organs of dolphins, used as love charms or aphrodisiacs when prepared in a special manner (da Silva and Best 1994, 1996; Trujillo and Diazgranados 2002; Alves and Rosa 2008). According to V. da Silva (pers. comm.), this market is no longer a significant threat in the Brazilian Amazon, although according to M. Borobia (in IWC 2007) the practice of selling dolphin parts continues in at least some local areas. However, according toV. Da Silva (pers. comm.), fishermen in the central Amazon do not kill tucuxi deliberately or use parts of its body as love charm. Teeth, eyes and body parts are from S. guianensis, most captured accidentally in the Para coast. Eyes of S. guianensis, killed in the nets at the Amazon estuary are often sold in the markets as Boto eyes. Recent molecular analyses have shown that a high proportion of dolphin products sold as amulets and love charms are derived from Guiana dolphins (S. guianensis), even in the Amazon region (Cunha and Solé- Cava 2007, Gravena et al. 2008, Sholl et al. 2008).

Recently, Loch et al. (2009) found two Tucuxis and one Boto wounded by perforating and cutting objects, probably harpoons and machetes. Such kills indicate potential conflicts with locals using tucuxi and boto as bait in a catfish fishery (V. da Silva, pers. comm.). Trujillo and Diazgranados (2002) reported one death by harpooning in the Colombian Amazon, in a ten-year monitoring period.
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The tucuxi dolphin is regularly caught accidentally in gillnets of large fishing trawlers, and is the most common cetacean in the by-catch of coastal fisheries in the south Caribbean Sea. Intentional hunting appears to be rare, but does take place for meat to eat, for blubber to be used as shark bait, and for the genital organs and eyes which are sold as love amulets (1). A major potential threat is a proposal for the construction of hydroelectric dams, which would cause population fragmentation and increased inbreeding, as well as the extinction of the migratory fish that constitute the diet of the freshwater tucuxi dolphin (2). Pollution from heavy metals, banned pesticides and noise are also concerns, as is habitat loss (1).
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Management

Conservation Actions

Conservation Actions

Sotalia fluviatilis is listed in Appendix I of CITES and in Appendix II of CMS. The species is legally protected in most of the range countries.

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Conservation

The superstition of fishermen, who believe the tucuxi dolphin to be a sacred animal that brings the bodies of drowned people back to the shore, has ensured that it has rarely been targeted as a food item (6). In 1994, the International Whaling Commission's (IWC) Scientific Committee urged member states to reduce by-catch and monitor populations (1). The IWC had previously started the Sotalia Project with the organisation 'Brasil's Biologists', which sets out to study the behaviour and habitat needs of the tucuxi dolphin, and has managed to build a significant collection of photo identifications (6).
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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Negative

There are no known adverse effects of Tucuxis on humans.

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Economic Importance for Humans: Positive

Indigenous South Americans hold Tucuxis in high regard as protectors that carry the drowned to shore for burial. Despite Brazilian law protecting them, Tucuxis are illegally hunted for their meat (bait), oil (emulsion to protect boats from water), and various body parts that are used in traditional medicines or religious ceremonies.

Positive Impacts: body parts are source of valuable material; source of medicine or drug

  • Alves, R., I. Rosa. 2008. Use of Tucuxi Dolphin Sotalia fluviatilis for Medicinal and Magic/Religious Purposes in North of Brazil. Human Ecology, 36/3: 443-447.
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Risks

IUCN Red List Category

Data Deficient (DD)
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Wikipedia

Tucuxi

The tucuxi (Sotalia fluviatilis), alternately bufeo gris or bufeo negro (both in Peru) is a dolphin found in the rivers of the Amazon Basin. The word tucuxi is derived from the Tupi language word tuchuchi-ana, and has now been adopted as the species' common name. Despite being found in geographic locations similar to those of 'true' river dolphins, such as the boto, the tucuxi is not closely related to them genetically. Instead, it is classed in the oceanic dolphin family (Delphinidae). Physically, the species, particularly the marine variety, resembles the bottlenose dolphin. However, this species is sufficiently different from the bottlenose dolphin that it is given its own genus, Sotalia. Animals formerly called the tucuxi occurring in coastal and estuarine environments have recently been recognized as a distinct species, the costero (Sotalia guianensis), also known as the pink dolphin.

Contents

Description

The tucuxi is frequently described (see references below) as looking similar to the bottlenose dolphin, but it is typically smaller at around 1.5 m (4.9 ft). The dolphin is colored light to bluish grey on its back and sides. The ventral region is much lighter, often pinkish. The dorsal fluke is typically slightly hooked. The beak is well-defined and of moderate length. There are 26 to 36 pairs of teeth in the upper and lower jaws.

[2]

Taxonomy

The tucuxi Sotalia fluviatilis was described by Gervais and Deville in 1853, and the costero Sotalia guianensis by Pierre-Joseph van Bénéden in 1864. These two species were subsequently synonymized, with the two species being treated as subspecies of marine and freshwater varieties.[3] The first to reassert differences between these two species was a three-dimensional morphometric study of Monteiro-Filho and colleagues.[4] Subsequently, a molecular analysis by Cunha and colleagues[5] unambiguously demonstrated that Sotalia guianensis was genetically differentiated from Sotalia fluviatilis. This finding was reiterated by Caballero and colleagues[6] with a larger number of genes. The existence of two species has been generally accepted by the scientific community.

Jumping Sotalia in the Orinoco river

Distribution

The tucuxi exists along much the length of the Amazon River and many of its tributaries, and is found in Brazil, Peru, southeastern Colombia, and eastern Ecuador. Numerous individuals have been seen in the Orinoco River further north, though it is not clear whether these are tucuxi or costero.

Behavior

The tucuxi exists in small groups of about 10-15 individuals, and swim in tight-knit groups, suggesting a highly developed social structure. Tucuxis are quite active and may jump clear of the water (a behavior known as breaching), somersault, spy-hop or tail-splash. They are unlikely, however, to approach boats.

Tucuxis have been observed to feed with other river dolphins. They feed on a wide variety of fish. Studies of growth layers suggest the species can live up to 35 years.

Conservation

The tucuxi is endemic to the regions described above; although no precise estimates of population are available, it is common. A significant human problem are fishing nets. Deliberate hunting in the Amazon Basin for food has also been reported. Pollution, in particular mercury poisoning of water due to gold mining, is a particular concern for this species.

Tucuxis are observed not to maintain good health and attitude in captive environments. A few tucuxis remained in captivity in European aquaria, but the last one ("Paco") died in 2009 in the Zoo of Münster, Germany.

The tucuxi is listed on Appendix II[7] of the Convention on the Conservation of Migratory Species of Wild Animals (CMS). It is listed on Appendix II[7] as it has an unfavourable conservation status or would benefit significantly from international co-operation organised by tailored agreements.

See also

References

  1. ^ Reeves, R.R., Crespo, E.A., Dans, Jefferson, T.A., Karczmarski, L., Laidre, K., O’Corry-Crowe, G., Pedraza, S., Rojas-Bracho, L., Secchi, E.R., Slooten, E., Smith, B.D., Wang, JY. & Zhou, K. (2008). Sotalia fluviatilis. In: IUCN 2008. IUCN Red List of Threatened Species. Retrieved 25 February 2009. Includes a lengthy justification of the data deficient category. Treats Sotalia fluviatilis and Sotalia guianensis as subspecies.
  2. ^ Monteiro-Neto, Cassiano; Alves-Júnior, Tarcísio Teixeira; Ávila, Francisco J. Capibaribe; Campos, Alberto Alves; Costa, Alexandra Fernandes; Silva, Cristine Pereira Negrão; Furtado-Neto, Manuel A. Andrade (2000). "Impact of fisheries on the tucuxi (Sotalia fluviatilis) and rough-toothed dolphin (Steno bredanensis) populations off Ceara state, northeastern Brazil". Aquatic Mammals (European Association for Aquatic Mammals) 26 (1): 49–56. ISSN 1996-7292. OCLC 55134873. Retrieved January 2013. 
  3. ^ Borobia, M., S. Siciliano, L. Lodi, and W. Hoek (1991). "Distribution of the South American dolphin Sotalia fluviatilis". Canadian Journal of Zoology 69 (4): 1024–1039. doi:10.1139/z91-148. 
  4. ^ Monteiro-Filho, E. L. D. A., L. Rabello-Monteiro, and S. F. D. Reis (2008). "Skull shape and size divergence in dolphins of the genus Sotalia: A morphometric tridimensional analysis". Journal of Mammalogy 83: 125–134. doi:10.1644/1545-1542(2002)083<0125:SSASDI>2.0.CO;2. 
  5. ^ Cunha, H. A., V. M. F. da Silva, J. Lailson-Brito Jr., M. C. O. Santos, P. A. C. Flores, A. R. Martin, A. F. Azevedo, A. B. L. Fragoso, R. C. Zanelatto, and A. M. Solé-Cava (2005). "Riverine and marine ecotypes of Sotalia dolphins are different species". Marine Biology 148 (2): 449–457. doi:10.1007/s00227-005-0078-2. 
  6. ^ Caballero, S., F. Trujillo, J. A. Vianna, H. Barrios-Garrido, M. G. Montiel, S. Beltrán-Pedreros, M. Marmontel, M. C. Santos, M. R. Rossi-Santos, F. R. Santos, and C. S. Baker (2007). "Taxonomic status of the genus Sotalia: species level ranking for "tucuxi" (Sotalia fluviatilis) and "costero" (Sotalia guianensis) dolphins". Marine Mammal Science 23 (2): 358–386. doi:10.1111/j.1748-7692.2007.00110.x. 
  7. ^ a b "Appendix II" of the Convention on the Conservation of Migratory Species of Wild Animals (CMS). As amended by the Conference of the Parties in 1985, 1988, 1991, 1994, 1997, 1999, 2002, 2005 and 2008. Effective: 5th March 2009. Convention on Migratory Species page on the Tucuxi
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