Showing posts with label Columbia. Show all posts
Showing posts with label Columbia. Show all posts

Wednesday, 31 December 2014

A new species of Olingo from the cloud forests of Colombia and Ecuador.


Olingos, Bassaricyon, are small members of the Racoon family, Procyonidae, found in Central and South America. They are not well understood, as they live in the canopy of dense forests where they are not easily observed, and are easily mistaken for the related Kinkajou, Potos flavus.

In a paper published in the journal ZooKeys on 15 August 2013, a team of scientists led by Kristofer Helgen of the Division of Mammals at the National Museum of Natural History in Washington DC describe a new species of Olingo from the cloud forests of Colombia and Ecuador.

The new species is named Bassaricyon neblina, which means ‘fog’ or ‘mist’ in Spanish, a reference to the cloud forests where it lives; Helgen et al. also suggest the common name Olinguito, meaning ‘Little Olingo’. The species was discovered during a genetic study intended to determine the relationships between the four previously described species of Olingo and other members of the Racoon Family, using DNA from museum specimens.

Surprisingly, despite all the specimens referred to the new species having previously been assigned to other species, the new species emerged as a distinct lineage, which was the sister group to all the other species (i.e. all the other species were more closely related to one another than to the new species). More surprisingly still, all the specimens found to belong to the new species were found to have been collected in cloud forests at altitudes of 1500-2750 m, while all the other specimens were from below 2000 m, suggesting a clear difference in habitat preference. They were also smaller and more slender than members of other species, with darker coats.

The Olinguito, Bassaricyon neblina, in life, in the wild. Taken at Tandayapa BirdLodge, Ecuador. MarkGurney in Helgen et al. (2013).

The Olinguito is found in cloud forests between 1500 m and 2750 m in montane cloud forests on the slopes of the Western and Central Andes in Colombia and Western Andes in Ecuador.

Distribution map for Bassaricyon neblina. Helgen et al. (2013).

See also…

Glyptondonts were large, heavily armored mammals related to Armadillos that evolved first appeared in South America in the Miocene, spread to North America in the Pliocene and became extinct at about the same time...

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Monday, 22 December 2014

Two new species of Electric Knifefish from the Amazonian river system.


Electric Knifefish, Hypopomidae, are small freshwater fish found in still and slow moving waterways in South America. They are members of the Order Gymnotiformes, which also includes the Electric Eel, Electrophorus electricus, and like it are capable of generating electrical pulses within their bodies, but unlike the Eel are not capable of producing a pulse of sufficient intensity to be used for capturing prey or defending against predators, though they are able to use it for sening and exploring their environment, and communicating with other members of the same species.

In a paper published in the journal ZooKeys on 28 August 2013, John Sullivan of the Cornell University Museum of Vertebrates, Jansen Zuanon of the InstitutoNacional de Pesquisas da Amazônia, and Cristina Cox Fernandes, also of the Instituto Nacional de Pesquisas da Amazônia and of the Biology Department at the Universityof Massachusetts, describe two new species of Electric Knifefish from the Amazon river system.

Both the new species are placed in the genus Brachyhypopomus, which is distinguished by having notably shorted snouts than other members of the Family Hypopomidae, but whereas other members of the genus, and indeed family, are toothless, the two new species were found to have small, needle-like teeth on their premaxillae (the bone that forms the front part of the upper jaw). For this reason Sulivan et al. erect a new subgenus, Odontohypopomus (‘Tootherd Knifefish’), in which both the new species are placed.

The first new species is named Brachyhypopomus (Odontohypopomus) walteri, in honour of Walter Heiligenberg (1938–1994) of the Scripps Institute of Oceanography, for his work on the neurophysiology and behaviour of electric Fish. The species was found in ‘floating meadow’ ecosystems along the Amazon and Solimões River systems, from the Río Napo drainagealong edge of Lago Anangucocha in Ecuador to the mouth of the Amazon River.

Specimen of Brachyhypopomus walteri, (total length 163 mm, length to end of anal fin 126 mm), sex undetermined,Paraná do Paracuúba, Amazonas, Brazil. Preserved whole specimen shown above close-up view of specimen immediately post-mortem. Scale bars equal 1 cm. Sullivan et al. (2013).

Adult specimens of Brachyhypopomus (Odontohypopomus) walteri examined range from 116 mm to 175 mm in length. They are yellow in colour and semi-transparent, with their gills appearing cherry red through the body wall, while the gut is dark and the swim bladder light. Many specimens had banding on their sides, which varied in both darkness and extent; in some specimens this was restricted to the dorsal side, in others the banding was also present on the underside, although narrower.

The second new species is named Brachyhypopomus (Odontohypopomus) bennetti, in honour of Michael Bennett of the Albert Einstein College of Medicine at Yeshiva University, for his work on electric fish neurophysiology. This species was also found in ‘floating meadow’ ecosystems, from Colombia, Ecuador and Peru in the west to the mouth of the Amazon in the east.

Specimen of Brachyhypopomus bennetti, (total length 215 mm, length to end of anal fin 171 mm), female,Paraná do Paracuúba, Amazonas, Brazil. Preserved whole specimen shown above close-up view of specimenimmediately post-mortem. Scale bars equals 1 cm. Sullivan et al. (2013).

Adult specimens of this species examined ranged from 98 mm to 215 mm in length. They were yellowish tan in colour, but not transparent, with similar banding to Brachyhypopomus (Odontohypopomus) walteri.

The two new species are very similar, and inhabit essentially the same environment. However one important way in which they do differ is in the electrical organ of Brachyhypopomus (Odontohypopomus) bennetti, which is considerably larger than that of Brachyhypopomus (Odontohypopomus) walteri, or indeed most Knifefish, and produces a monophasic electrical pulse (a short burst of positive charge) rather than a diphasic electrical pulse (a short burst of positive charge followed by a short phase of negative charge) as seen in most Gymnotiforme Fish.

Effect of loss of caudal portion of body by predation on electric organ discharge (EOD)waveform in three species of Brachyhypopomus. Undamaged individuals indicated by black dots and blackEOD trace, those with regenerating caudal body following substantial injury with red (A) Brachyhypopomus pinnicaudatus specimens 93-20 (above) and 93-25 (below) (B) Brachyhypopomus walterispecimens 93-188/2 (above) and 93-187-1(below). Damaged specimen 93-140 (blue trace) not shown (C) Brachyhypopomus bennetti specimens 93-37/1 (above) and 93-37/3 (below). EODs shown with head positivity upwards and amplitude-normalized. Sullivan et al. (2013).

It has previously been speculated that variations in the electrical emissions of Gymnotiforme Fish may reflect variations in water conductivity, but the two species of Odontohypopomus live alongside one-another, so this seems unlikely to be the case in this instance. A monophasic pulse has only been recorded in two other species of Gymnotiformes, one of which is the Electric Eel, Electrophorus electricus, which occurs in the same floating meadows as the two Odontohypopomus species, and which is predatory in nature. Sullivan et al. suggest that Brachyhypopomus (Odontohypopomus) bennetti may be able to use its monophasic pulse to fool Electric Eels, or other predators which avoid dangerous Electric Eels but consume Knifefish.

The habitat of Brachyhypopomus (Odontohypopomus) walteri and Brachyhypopomus (Odontohypopomus) bennetti. Paraná do Paracuúba, south of Manaus, Brazil, approximately 03°12.6'S, 59°59.4'W. Sullivan et al. (2013).

However Sullivan et al. also note that Knifefish frequently lose their tails due to predation and that this causes their electrical pulses, in particular the second, negative, phase of their pulses, to become much weaker. They also not that the electrical pulses of  Brachyhypopomus (Odontohypopomus) bennettiis not affected by the lose of its tail, and suggest that the monophasic pulse might be an adaptation that lets the Knifefish endure such attacks with less loss of electrical pulse function.

See also…

Cichlid Fish of the genus Apistogramma are found in waterways across tropical South America. There are currently 84 known species, of which 18 are found in the Peruvian Amazon Basin. They are small Fish, never exceeding 60 mm in length, the males growing larger than the females and typically being more brightly coloured. 
Armoured Catfish (Loricariidae) are distinctive Catfish (Siluriformes) with bodies covered in bony armoured plates found only in South America. They are a diverse group, with a high number of species, many of which have very limited distributions, and several new...
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A new species of Frog Crab from the Early Cretaceous of Colombia.


Frog Crabs, Raninoidia, are well represented in the fossil record across much of the globe in the Late Cretaceous and Cenozoic, but poorly recorded from the Early Cretaceous, when the group is thought to have originated. For a long time the majority of early Frog Crabs known were from Eurasia, leading to suggestions that they may have originated at high northern latitudes, but a number of new specimens have recently been reported from Colombia, leading to a re-evaluation of the groups origins, with the possibility that they may have originated in equatorial South America.

In a paper published in the journal Scripta Geologica in October 2014, Javier Luque of the Department of Biological Sciences at the Universityof Alberta and the Smithsonian Tropical Research Institute described a new species of Frog Crab from the Early Cretaceous Paja Formation of the Department of Santander in Colombia.

The new species is named Bellcarcinus aptiensis, where ‘Bellcarcinus’ means ‘Bell’s Crab’ honouring palaeontologist Thomas Bell (1792-1880) for his work on fossil Frog Crabs, and ‘aptiensis’ means ‘from the Aptian’, in reference to the Aptian Age (~125-113 million years ago), from which the fossils derive.

Bellcarcinus aptiensis, dorsal carapace. Luque (2014).

The new species is described from four specimens, ranging from 6.6 mm to 13 mm in length and from 8 mm to 16.1 mm in width. Luque suggests that Bellcarcinus aptiensis is probably a member of the Orithopsidae, making it the earliest occurrence of a group already thought to be one of the earliest Frog Crab families to appear, but notes that it also shows affinities to the Necrocarcinidae.

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http://sciencythoughts.blogspot.co.uk/2014/12/a-new-species-of-pea-crab-from-st-johns.html A new species of Pea Crab from St. John’s Island, Singapore.                                                               Pea Crabs of the genus Indopinnixa are found living commensally in the burrows of Sipunculan Worms across South and Southeast Asia. They are morphologically quite variable, with different species having different carapace structures and numbers of fused segments, but all are quite small, which gets the...
Crabs are Decapod Crustaceans related to Shrimps...
Freshwater Crabs of the genus Geothelphusa, are known from Taiwan, the Ryukyu Islands and the main islands of Japan. To date 55 species have been described, 38 of which are found in Taiwan and its adjacent islands, fifteen are found in the Ryukyus and...


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Thursday, 6 November 2014

Four new species of Treerunner from northern South America.


Treerunners of the genus Plica are Iguanid Lizards found in South America east of the Andes. They are medium sized, conspicuous Lizards that are active in the daytime, living in small colonies on rock outcrops or trees, and therefore are well represented in museum collections, as they tend to attract the attention of collectors. There are four species currently recognized, though two of these are considered to be both widespread and morphologically variable, making it likely that there are a number of cryptic species (species that cannot easily be differentiated from similar species by simple visual examination, but which are nevertheless reproductively isolated) within the group.

In a paper published in the journal ZooKeys on 25 November 2013, John Murphy of the Field Museum of Natural History in Chicago and Michael Jowers of the Departamento de Etología y Conservación de laBiodiversidad at the Estación Biológica de Doñana describe four new species of Treerunner, from populations previously described as Plica plica.

The first new species described is named Plica caribeana, in reference to its distribution, on the Caribbean coast of Venezuela and the islands of Trinidad and Tobago. Plicac aribeana has a lower number of dorsal scale rows than Plica plica, 92-125 as opposed to 126-140, and was confirmed to be a separate species by genetic analysis. It is mottled green and brown in colour, with distinctive black markings, females tend to be slightly larger than the males. The species lives in colonies of 6-15 individuals in forests or forest edges, and is frequently observed on trees, rock-faces, buildings and even in caves. The species is insectivorous, feeding on Ants, Beetles, Spiders, Cicadas and other Arthropods, and itself appears to be a favoured prey item of the Tropical Flat Snake Siphlophis compressus. Females lay clutches of two eggs.

 Plica caribeana, from the Arima Valley of Trinidad. Murphy & Jowers (2014).

The second new species is named Plica kathleenae, in honour of the herpetologist Kathleen Kelly of the Division of Amphibians and Reptiles at the Field Museum of Natural History. The species is described from a single male specimen collected by Emmet Reid Blake near the headwaters of the Itabu Creek in the Sierra Acarai Mountains of Guyana, close to the border with Brazil, during the Sewell Avery British Guiana Expedition of 1938. The specimen has 158 dorsal scale rows at mid body (considerably more than Plica plica) and is a dark brown colour with dark and light spots; though this is its colouration preserved in alcohol, and probably differes from the colouration of the living animal.

The head of Plica kathleenae in dorsal view. Murphy & Jowers (2014).

The third new species described is named Plica medemi, in honour of Colombian herpetologist Fredrico Medem, who collected the single known specimen of this species at Cerro de las Pinturas in Colombia in 1957. This species is also described from a single male specimen, with 145 dorsal scale rows at mid body. The specimen is green with dark spots and an orange head; since it is preserved in alcohol it was most likely more strikingly coloured in life.

The head of Plica medemi in dorsal view. Murphy & Jowers (2014).

The final new species described is named Plica rayi, in honour of Ray Pawley the former Curator of Reptiles at Brookfield Zoo, for his lifelong work with Reptiles and Amphibians. This species has 182-202 dorsal scale rows at mid body (considerably more than any other member of the group. The Lizards are a dark brown colour with black and white markings, the males develop red or orange markings on their faces in the breeding season. The species is known from colonies at two sites on the Orinoco River, at Puerto Ayacucho in Venezuela and at Puerto Carreno in Colombia, and has been seen at other sites along the river. The species is found in granitic rainforests (i.e. rainforests standing on granite-derived soils), and favours rocky areas. The breeding season is in May.

Plica rayi. A male in breeding coloration. Photographed at Tobogan de la Selva, Puerto Ayacucho. Zelimir Cernelic in Murphy & Jowers (2014).

See also…

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Monday, 13 October 2014

A new species of Bush Currant from Columbia.


Bush Currants, Miconieae, are berry producing tropical trees and shrubs in the Melanastome Family, Melastomataceae. They are found throughout the tropics but at their most diverse in Colombia, where over 490 species have been described.

In a paper published in the journal Phytotaxa on 29 August 2014, Diana Gamba, Frank Almeda and Marcela Alvear of the Institute for BiodiversityScience and Sustainability at the Department of Botany at the CaliforniaAcademy of Sciences describe a new species of Bush Currant from the western cordillera in the Chocó biogeographic region of Colombia.

The new species is placed in the genus Miconia and given the specific name indicoviolacea, in reference to the violet and blue colour of its flowers. Miconia indicoviolacea is a small shrub reaching about one meter in height. It has dark green leaves and greenish stems, and produces bluish flowers and berries. The plant was only observed in January and February, when it was producing both flowers and fruit.

Miconia indicoviolacea, general habit. Marcela Alvearin Gamba et al. (2014). 

Miconia indicoviolacea has only been recorded from two sites on the western flank of the Cordillera Occidental, one in the Farallones de Cali National Park and the other within the Reserva Natural de las Aves El Pangán. These parks have a combined area of 2670.7 km3, however they are in a mountainous region and contain land with altitudes ranging from 200 to 4100 m, and Miconia indicoviolacea has been found growing only at altitudes of 600-700 m (this is quite common, many plants and animals have restricted altitude tolerances, particularly in the tropics), suggesting that the available growing range of the plant is much smaller than the area of the parks – probably only about 12 km3. As such Gamba et al. suggest that the species should be considered to be Endangered under the terms of the International Union for the Conservation of Nature’s Red List of Threatened Species.

Flowers (top) and fruit (bottom) of Miconia indicoviolacea. Marcela Alvearin Gamba et al. (2014).

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Sunday, 14 September 2014

Number of Saki Monkey species raised from five to sixteen.

Saki Monkeys of the genus Pithecia are found throughout the tropical forests of South America. The taxonomy of the group is poorly understood, as species are often both variable and similar to other species and hard to observe in the wild, favouring old growth and often flooded forests. Many species were described in the nineteenth and early twentieth century by taxonomists working in European museums, with little or no information on where the specimens were collected, and only a limited understanding of the life histories of the living animals. 

Female Saki Monkeys tend to be slightly smaller than males, but not to a great enough extent that this feature can be used to determine sex. More reliable is colouration, with adult males of most species having a distinctive coat that separates them from the females. However only fully adult males have this coat, with sub-adults resembling females, then going through an intermediate phase as they develop their male colouration, which can be mistaken for a completely different species. Since it can be hard to determine the sex of living Saki Monkeys by physical examination, this presented a considerable obstacle to nineteenth century taxonomists working from preserved specimens of unknown or inaccurately recorded origin (many early collectors in South America simply bought specimens from local hunters in large towns without worrying about where they came from; some may have lied about the origin of their specimens when selling them on to museums in order to increase their value).

The behaviour of the Monkeys does little to help this situation. They tend to live in dense and inaccessible forests, and for the most part will avoid contact with humans. They live in small family groups, often with subadult females as well as younger offspring, and when threatened the adult female will often sit on a conspicuous branch with an older juvenile female to observe the threat, while younger members of the group hide and the male circles round shaking vegetation to create a diversion. Thus observations of ‘pairs’ of Saki Monkeys are typically of an adult and subadult female.

Like most primate groups, Saki Monkeys are quite well studied today, but largely by ecologists rather than taxonomists. Ecologists for the most part have little taste for taxonomy, which tends to involve the extensive study of dead specimens in museums. However understanding the taxonomy of a group is vitally important for long-term conservation, as it is impossible to accurately determine population sizes or distribution if it is not possible to determine whether populations belong to the same or different species.

The last major review of the taxonomy of Saki Monkeys was carried out in 1987, when Phillip Hershkovitz of the Field Museum of Natural History in Chicago split the genus into five species and several subspecies (expand). 

In a paper published in the journal Neotropical Primates in July 2014, Laura Marsh of the Global Conservation Institute in Santa Fe, New Mexico, undertakes a complete review of the genus Pithecia, concluding that there are in fact sixteen species. In doing this she reinstates three previously described species, promotes three subspecies to full species level, and erects five new species.

The White-faced Saki, Pithecia pithecia, was first described in 1766 by Swedish naturalist Carlus Linnaeus (under the name Simia pithecia, Saki Monkeys were not placed in a separate genus till 1804). The name has remained in use till today, though museum specimens have been described as a number of other species, and other species have been described as Pithecia pithecia. Adult male White-faced Sakis are more-or-less completely black, with white ‘half-moon’ facial disks. Females are brownish or greyish and may have white striping, and have orange chest hair, the colour of which varies in intensity in different populations. White-faced Sakis are found in Venezuela, Guyana, French Guiana, and Suriname, and in the Brazilian states of Roraima, Amapá and Pará. 

The White-faced Saki, Pithecia pithecia. Marsh (2014).

The Golden-faced Saki, Pithecia chrysocephala, was first described in 1850 by Geoffroy Saint-Hilaire of the Museum d’Histoire Naturelle in Paris, but has been considered to be a subspecies of either Pithecia pithecia or Pithecia monacha for most of the last century. March re-elevates this group to full species level. Golden-faced Sakis resemble White-faced Sakis, but the face plates of the males are deep orange or reddish brown in colour. The Golden-faced Saki is found only in Brazil north of the Amazon.

The Golden-faced Saki, Pithecia chrysocephala. Marsh (2014).

The Hairy Saki, Pithecia hirsuta, was first described in 1823 by Johann Baptist von Spix of the Zoologische Staatssammlung in Munich, with the name remaining in use till today. This species shows little colour variation between the sexes, with both being black with some white stripping and some brown on the chest. The species is found in Brazil, Peru and Columbia between the Río Napoin and Rio Solimões in the south, the Río Caquetá and Rio Japurá in the north and Rio Negro to the east.

The Hairy Saki, Pithecia hirsuta. Marsh (2014).

Miller’s Saki, Pithecia milleri, was first described by Joel Allen of the American Museum of Natural History in 1914, but was reclassified as a subspecies of Pithecia monachus by Hershkovitz in 1987. Marsh re-elevates this taxon to full species status. Miller’s Saki resembles the Hairy Saki, but is more grizzled (greyer). The females are more distinctive in this species, being paler and shaggier than the males. Miller’s Saki is found in southwest Columbia and northeast Ecuador, and may also be present in neighbouring areas of Peru, though it has not been reported there.

Miller’s Saki, Pithecia milleri. Marsh (2014).

The Monk Saki, Pithecia monachus, was first described by Geoffroy Saint-Hilaire in 1812, and has been accepted as a valid species ever since, though several other species have been treated as members of this species at times. Males of this species tend to be black, with a little white stippling, mostly on the forearms and chest, and brown hair on the face. Females are more grizzled than the males, with brown hair only on the forehead. The species is found in eastern Peru and western Brazil.

The Monk Saki, Pithecia monachus. Marsh (2014).

The Burnished Saki, Pithecia inusta, was first described in 1824 by Johann Baptist von Spix, but was thought to be a population of Pithecia monachus by Hershkovitz in 1987. Marsh re-elevates this to full species status. Males are black with lighter stippling, the ruff is brown, with lighter brown hair tips, and can be buff or almost orange in older individuals. The face is an off-white colour. Females are similar to males, but with more white in their coats. 

The Burnished Saki, Pithecia inusta. Marsh (2014).

Cazuza’s Saki, Pithecia cazuzai, is a new species erected by Marsh, to describe three populations formerly assigned to the species Pithecia irrorata (Grey’s Bald Faced Saki). It is named in honour of the Brazilian primatologist José de Sousa e Silva-Júnior, (known as ‘Cazuza’), of the Museu Paraense Emílio Goeldi, for his contribution to South American taxonomy. Both sexes are black with white grizzling, the females being darker and less grizzled than the males. The species is known only from Brazil around the Rio Juruá.

Cazuza’s Saki, Pithecia cazuzai. Marsh (2014).

The Equatorial Saki, Pithecia aequatorialis, was first described by Philip Hershkovitz in 1987. The males are black, with grizzled white tips to their hairs, a horseshoe-shaped white band around the face and an orange ruff. Females are greyer and more grizzled, with a less pronounced ruff. The species is found in Peru, south of the Río Napo and Río Curaray and west of the Río Tigre.

The Equatorial Saki, Pithecia aequatorialis. Marsh (2014).

The Napo Saki, Pithecia napensis, was first described by  Einar Lönnberg of the Swedish Museum of Natural History as a subspecies of Pithecia monachus, though Hershkovitz did not accept that this was a valid taxon at all. Marsh re-introduces it, and elevates it to full species. Males are black, with grizzled white tips to their hair, a distinctive whit crown on the head and a white facial disk surrounding the face, fading to grey towards the bottom. The ruff is rusty or even bright orange. Females are greyer, with a brown ruff. The species is found in northeast Ecuador and northern Peru.

The Napo Saki, Pithecia napensis. Marsh (2014).

Isobel’s Saki, Pithecia isabela, is a new species erected by Marsh to describe several populations of Saki Monkeys in northern Peru, formerly assigned to the species Pithecia monachus but now recognized as distinct. Pithecia isabela is named in honour of Isabel Grameson Godin des Odonais, who mounted an expedition into the forests of French Guyana in search of her lost husband in 1768. The males have black coats, often with a coppery sheen, and a dark rusty-orange ruff. The face is black, and surrounded by a ring of light brown hair in younger males, though as they get older it darkens to black. The facial disk is dark, but lighter grizzling which makes it appear grey or even white; there are also white patches above the eyes. Females are similar to males, with a black coat with a coppery sheen, though on females this is heavily grizzled. The hair of the ruff is black with brown tips and the facial disk black. 

Isobel’s Saki, Pithecia isobela. Marsh (2014).

The Buffy Saki, Pithecia albicans, was first described as a species by John Edward Gray of the British Museum of Natural History (now the Natural History Museum) in 1860, and has been recognized as a valid species ever since. This is a very distinctive species, larger than other members of the genus and covered in blond or orange fur, except for the back and tail, which are black. This species is found only in Brazil, between the lower Rio Purus and Rio Tefé and the Rio Solimões-Amazonas in Amazonas State.

The Buffy Saki, Pithecia albicans. Marsh (2014).

Gray’s Bald Faced Saki, Pithecia irrorata, was first described by species by John Edward Gray of the British Museum of Natural History (now the Natural History Museum) in 1842, and has been recognized as a valid species ever since. These Sakis are black with heavily grizzling that makes them appear grey or even whitish all over. The males have a white band or crown above the face, which is hairless and pink. This species is known from Peru and Brazil, though the known populations are somewhat scattered, and its full distribution is probably not known.

Gray’s Bald Faced Saki, Pithica irrorata. Marsh (2014).

Vanzolini’s Bald Faced Saki, Pithecia vanzolinii, was first described by Philip Hershkovitz in 1987. These are black or dark grey on their backs and tails, with cream or yellowish bellies and limbs. The males have a thicker coat than the females. This species is known only from southwest Brazil.

Vanzolini’s Bald Faced Saki, Pithica vanzolinii. Marsh (2014).

Mittermeier’s Tapajós Saki, Pithecia mittermeieri, is a new species named by Marsh in honour of Russell Mittermeier, President of Conservation International and long-time Chairman of the International Union for the Conservation of Nature Species Survival Commission’s Primate Specialist Group. The species comprises populations found south of the Rio Amazonas between the Rio Madeira and Rio Tapajós in Brazil, which were formerly assigned to Pithecia irrorata. These have black coats, but heavily grizzled with white hair, making them appear almost white, males have black faces and both sexes tend to get darker as they get older.

Mittermeier’s Tapajós Saki, Pithecia mittermeieri. Marsh (2014).

Ryland’s Bald-faced Saki, Pithecia rylandsi, is a new species named by Marsh in honour of Anthony Rylands, Senior Research Scientist at Conservation International, Deputy Chair of the International Union for the Conservation of Nature Species Survival Commission’s Primate Specialist Group, a member of the Brazilian Academy of Sciences, former professor of Vertebrate Zoology at the Federal University of Minas Gerais, and founding editor for the journal Neotropical Primates. The species comprises populations of Sakis from southern Peru, northwest Bolivia and southwest Brazil, which have formerly been assigned to several other species. These have black coats heavily grizzled with white, but turn completely white as they age. The faces are black in both sexes.

Ryland’s Bald-faced Saki, Pithecia rylandsi. Marsh (2014).

Pissinatti’s Bald-faced Saki, Pithecia pissinattii, is a new species named by Marsh in honour of Alcides Pissinatti, a Brazilian veterinarian, director and co-founder of the Centro de Primatologia do Rio de Janeiro as well as Vice President of the Brazilian Academy of Veterinary Sciences, for his work on captive breeding programs of Saki Monkeys. The species comprises populations in Brazil previously assigned to Pithecia irrorata and Pithecia hirsuta. These are very grizzled Sakis with bare faces, the males become brownish with age.

 
Pissinatti’s Bald-faced Saki, Pithecia pissinattii. Marsh (2014).

The approximate distributions of the Saki Monkeys, Pithecia, following the classification proposed. Stephen Nash in Marsh (2014).

See also…

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 A fossil Ape from the Late Miocene of Yunnan Province China.

Apes (Hominoidea) are large, tailless Primates found in Africa, eastern Asia, and in one case (Homo sapiens) globally. Apes are commonly divided into Lesser and...


 Burmese Snub-nosed Monkey found in China.

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