User:Di Whitt/Azaras's capuchin
Azaras's capuchin or hooded capuchin (Sapajus cay) is a species of robust capuchin. It occurs in eastern Paraguay, southeastern Bolivia, northern Argentina, and Brazil, at Mato Grosso do Sul and Mato Grosso states, in Pantanal.Its habitat consists of subtropical, humid, semi-deciduous, gallery forests and forested regions of the pantanals. Formerly, it was considered a subspecies of black-striped capuchin, according to Groves (2005) with the name Cebus libidinosus paraguayanus, but Silva Jr. (2001) considered it a separated species. They are considered as frugivores-insectivores which means that their diet mainly consists of a variety of fruits, seeds, arthropods, frogs, small mammals, etc.[1]
Evolution and Taxonomy
[edit]Cebus and Sapajus have been widely recognized as subgenera–or groups–of the capuchin monkey’s subfamily Cebinae. There is data hinting towards an estimated separation time between these two subgenera of about 6.2 million years.[2] Evidence indicates that during the Miocene, these two groups diverged from each other due to the emergence of the Amazon river; Cebus (gracile capuchin) expanded northwards towards the Amazon rainforest, and Sapajus (robust capuchin) expanded southwards towards the Atlantic forest.[2] However, during the Pleistocene, Sapajus expanded northwards once again towards the Amazon, becoming sympatric with Cebus. Nowadays, supported by ample evidence, it is accepted that Sapajus and Cebus are two different groups, and even considered two different genera.[3] Silva JS’s morphometric analysis categorized Sapajus species into three groups based on their geographical location; the Amazonian species, the species from central South America (south of the Cerrado and north of the Rio Doce), and the species of the Atlantic forest (south of the Rio Doce). Sapajus cay belongs to the second group.[1]
Phylogenetic analysis revealed that Sapajus cay was the product of the second divergence event (following Sapajus nigritus robustus) that occurred in the Atlantic forest group before the Sapajus expansion towards the Amazon during the Pleistocene.[3] However, the true current distribution of the Sapajus cay is a matter of debate between leading parties, and it is mainly due to the phenotypic characteristics of populations that live in different geographical locations.[4]
Characteristics
[edit]Azara’s capuchin monkeys are considered as one of the tufted capuchins, but the tuft will fully develop only after the individual reaches adulthood. Sexual maturity is estimated to be reached at the age of 4-5 years old for females, and around 8 years old for males. In captivity, individuals can live up to 50 years, while in the wild the average is around 30 years.[5]
This species of capuchin monkey presents slight sexual dimorphism; the male being larger in body size.[6] The female weighs between 1.4-3.4 kg, whereas the male can weigh between 1.3-4.8 kg.[7] The average male individual averages a height of 0.8m from nose to tail, while the female is slightly shorter. They posses long feet and tails; the tails can be as long as half their body height.[8] Another distinction from the rest of the Sapajus species–according to Silva–is that the S. cay has significantly smaller cranium size, even at adulthood.
Azara’s capuchins normally present medium-length fur with several different tones of brown throughout the body. Their limbs are usually a darker colour, as well as their tuft. Compared to the rest of the Sapajus species, the Azara’s capuchin exhibits a dark stripe of hair on the front of their ears, which resembles sideburns.[1]
There has been major disagreements on the true taxonomic nature of these species because of their high morphological variability. S. cay individuals exhibit inter and intra-population polymorphism, they also exhibit sexual dimorphism and significant changes in their morphology at different ages.[3]
Distribution and Habitat
[edit]The habitat of the capuchin’s monkey species, respectively Cebus and Sapajus, is located in the tropical and subtropical forests of South and Central America.Though they occupy a wide range of territory, their population currently only reside on nearly 200 hectares (around 500 acres).[9] Their habitat is hot and humid all year round, with high quantity of precipitation and vegetation.They have a high level of behavioral as well as ecological flexibility, allowing them to reside in a wide range of habitats(Martins et al.,2015).In fact,the Sapajus cay species habitat is distributed among countries such as northern Argentina, south-eastern Bolivia, eastern Paraguay.
They also inhabit Brazil, where they are located southwest of the Amazon, approximately south to the states of Mato Grosso, Mato Grosso do Sul as well as southeast of Goi ́as state (Peixoto-Couto et al., 2021). Sapajus Cay monkeys reside in northern Argentina, in the provinces of of Jujuy, Salta, Formosa and Chaco (IUCN article). The Sapajus Cay species, also known as the hooded monkey, is the only representative of its genus established in the country of Paraguay(Smith, R. L. 2017). In fact, they live in the humid semi deciduous Upper Parana ́ Atlantic Forest of Paraguay (Secretaría de Ambiente , 2019).
Ecology and Behaviour
[edit]Azara’s capuchins are diurnal opportunistic omnivores, who live in social communities and travel throughout their territory looking for food.[10] Research indicates that these capuchins spend most of their time resting, travelling and foraging. While there were significant differences in the behaviours of males and females, there were not many significant differences in their diet. Males were observed to spend more time on the ground or near it, resting and vigilating the area. Females, on the other hand, spend significantly more time browsing and eating on the canopy of the sleeping trees.These difference in behaviours is attributed to the small–and only–difference in their diet. Males tend to eat larger objects than females (prey or plant matter); noticeably, only large males have been seen eating small vertebrates. This difference in the size of the meal is thought to be the reason why males spend more time resting (digesting), while the females spend more time foraging in order to compensate for the smaller size of their meals. [6]
The size of communities can vary greatly, some can be short of a dozen individuals, whereas some communities have been recorded to have up to 44 individuals.[6] Their communities consist of a multi-male/multi-female dynamic, with an alpha male who is usually the largest and most ferocious. This alpha male typically serves as a protective figure, who also controls the access to food, and has priority to mate with the females.[10] These communities normally travel continuously throughout a certain territory, without leaving its boundaries. Only under extreme conditions will they choose to explore new territories. Research indicates that these species have the ability to learn and retain information for long periods of time, which is a key quality for their high adaptability. Long-term memory serves as a tool in order to recognize patterns for profitable and dangerous phenomena. Tujage et al. (2015) were able to show that individuals can deduce that if one fruit tree is producing fruit, then all the others of the same species must be producing as well, so the individuals would actively look for these.[5]
Many behaviours similar to other capuchin species have been observed in some communities, but their exact reasons have not been concretely proven. Some individuals have been seen to rub the leaves of certain citrus trees on their fur, while exhibiting other protective behaviours. It is thought that this behaviour is triggered when threats are near, and the strong smell of the leaves play a part. [11]
Tool use has also been documented in S. cay individuals. Even though the consumption of hard shelled fruits and seeds is not preferred, it forms a large part of their diet. These capuchins hold the object with both hands, and smash it against tree branches that act as an anvil. High ranking adults are especially successful at this, while low ranking adults will sometimes wait for the leftovers of the processed food. [12]
Endangerment and Threats
[edit]To this day, it is reported that there are no major threats for the Sapajus cay species in Paraguay.Indigenous peoples hunt this specie for food as a survival purpose, but human population is low, hence not creating a significant threat.The only threat in Paraguay is forest loss due to anthropogenic causes or natural disasters.It is known that Sapajus cay monkeys are the most common kept primate pet in Paraguay,hence caring and protecting them (Stallings 1985 in IUCN article).
However in Brazil,the Sapajus cay species are listed as highly vulnerable(Júnior Oscar Fernandes, 2020). In fact, there are many extreme threats to the species survival rate. These major threats include fire, rural settlements, agriculture, livestock keeping, urban sprawl, vulnerability to epidemics, deforestation, increasing road and energy infrastructure, habitat isolation, habitat reduction, pollution, hunting and life capture for pet trade (Rímoli et al. 2015 in IUCN article).High Population density in areas Southand Central America as well as legal and illegal selective logging is destroying the Sapajus cay wildlife, ruining the fragment of forests they inhabit(Smith et al., 2018).
In addition, their populations inhabiting what is left of the Argentinian forest are subject to serious threats as a consequence of habitat modification and conversion for agriculture production, as well as poaching (illegal hunting).Industrialization led by humans has altered the natural environment, negatively affecting Argentina’s ecosystems. This can potentially result in pathogenic exchange,increasing the death rate of the Sapajus Cay species(Sanchez-Fernandez et al., 2022).
Conservation
[edit]In Brazil,The Azara’s capuchin monkey is not well studied, resulting in poor conservation actions due to lack of ecological knowledge of this species. The Sapajus cay species is in danger, with threat of extinction. Drastic regional conservation actions are required for their survival. (Júnior Oscar Fernandes, 2020).
In Argentina, the Azara’s capuchin is conserved and protected in these following areas;ArgentinaThe El Rey National Park Province of Salta(44,162 ha) ,the Calilegua National Park , the Province of Jujuy(76,000 ha), the Baritú National Park Province of Jujuy(72,000 ha) and the BoliviaKaa-Iya National Park. (IUCN article)
In Brazil, the Sapajus cay species are secured and preserved in these realms;the Pantanal Matogrossense National Park , the Serra da Bodoquena National Park (77,021 ha) ,the Rio Negro State Park (7,000 ha) , the Segredo Stream State Park (189 ha) ,the SESC Pantanal Private Reserve (RPPN) (106,31 ha),the Fazenda Acurizal Private Reserve (13,665 ha) ,the Fazenda Penha Private Reserve (RPPN) (13,409 ha),the Fazenda Boqueirão Private Reserve (RPPN) (173,60 ha) ,the Fazenda Singapura Private Reserve (RPPN) (456 ha) ,the Fazenda América Private Reserve (RPPN) (401 ha) ,the Fazenda Trevo Private Reserve (RPPN) (27,75 ha) (Wallace 2008),the Fazenda Floresta Negra Private reserve (RPPN) (971,06 ha),the Fazenda Nova Querência Private Reserve (50 ha in 8,500 ha of Gallery Forest) and the Fazenda São Marcos (600 ha) (IUCN article)
References
[edit]- ^ a b c Lynch Alfaro, J.W.; Silva, J.S. & Rylands, A.B. (2012). "How Different Are Robust and Gracile Capuchin Monkeys? An Argument for the Use of Sapajus and Cebus". American Journal of Primatology. 74 (4): 1–14. doi:10.1002/ajp.22007. PMID 22328205.
- ^ a b Alfaro, J. W. L., Boubli, J. P., Olson, L. E., Di Fiore, A., Wilson, B., Gutiérrez-Espeleta Gustavo A, Chiou, K. L., Schulte, M., Neitzel, S., Ross, V., Schwochow, D., Nguyen, M. T. T., Farias, I., Janson, C. H., & Alfaro, M. E. (2011). Explosive pleistocene range expansion leads to widespread amazonian sympatry between robust and gracile capuchin monkeys. Journal of Biogeography, 39(2), 272–288.
- ^ a b c Martins, A. M. G., Amorim, N., Carneiro, J. C., de Mello Affonso, P. R. A., Sampaio, I., & Schneider, H. (2015). Alu elements and the phylogeny of capuchin (cebus and sapajus) monkeys. American Journal of Primatology, 77(4), 368–375. https://doi.org/10.1002/ajp.22352
- ^ Lima, M. G. M., Buckner, J. C., Silva-Júnior José de Sousa e, Aleixo, A., Martins, A. B., Boubli, J. P., Link Andrés, Farias, I. P., Silva, M. N., Röhe Fabio, Queiroz, H., Chiou, K. L., Di Fiore, A., Alfaro, M. E., & Lynch Alfaro, J. W. (2017). Capuchin monkey biogeography: understanding sapajus pleistocene range expansion and the current sympatry between cebus and sapajus. Journal of Biogeography, 44(4), 810–820. https://doi.org/10.1111/jbi.12945
- ^ a b Tujague, M. a, Janson, C. H., & Lahitte, H. c. (2015). Long-term spatial memory and learning set formation in captive capuchin monkeys (cebus libidinosus = sapajus cay). International Journal of Primatology, 36(6), 1067–1085.
- ^ a b c Júnior Oscar Fernandes, Porfirio, G. E. de O., Santos, F. M., Gimenes Nantes, W. A., Oliveira de Assis, W., Braziliano de Andrade, G., Herrera, H. M., & Rímoli José. (2020). Behavioral activities and diet of azaras’s capuchin monkey, sapajus cay (illiger, 1815), in a forest remnant of the brazilian cerrado. Studies on Neotropical Fauna and Environment, 55(2), 149–154. https://doi.org/10.1080/01650521.2019.1708228
- ^ Nieves, Mariela; Peker, Silvana; Tujague, María Paula; Kowalewski, Martín; Pavé, Romina; Agostini, Ilaria; Alcalde, Ana Sofía; Albanesi, Sebastián; de Bustos, Soledad; Jayat, J. Pablo; Maras, Gustavo A.; Perovic, Pablo G.; Reppucci, Juan I.; Apellaniz, Melisa (2019). Sapajus cay. En: SAyDS–SAREM (eds.) Categorización 2019 de los mamíferos de Argentina según su riesgo de extinción. Lista Roja de los mamíferos de Argentina. Versión digital: http://cma.sarem.org.ar.
- ^ "Azaras's Capuchin data - Encyclopedia of Life". eol.org. Retrieved 2022-04-11.
- ^ Secretaría de Ambiente y Desarrollo Sustentable de la Nación y Sociedad Argentina para el Estudio de los Mamíferos (eds.) (2019). Categorización 2019 de los mamíferos de Argentina según su riesgo de extinción. Lista Roja de los mamíferos de Argentina. Versión digital: http://cma.sarem.org.ar.
- ^ a b Peixoto-Couto, R. M., Dos Santos, V. P., & Dias-Silva, F. (2021). Consumption of melopsittacus undulatus (shaw, 1805) (psittaciformes, psittacidae) by sapajus cay illiger, 1815 (primates, cebidae) in midwest region of brazil. Actualidades Biológicas, 43(115). https://doi.org/10.17533/udea.acbi.v43n115a01
- ^ Smith, R. L. (2017). An observation of an unusual human-directed threat display by sapajus cay illiger, 1815 (cebidae: primates) in a fragment of upper paraná atlantic forest, eastern paraguay. Mammalogy Notes, 4(1), 5–6. https://doi.org/10.47603/manovol4n1.5-6
- ^ Smith, R. L. (2017). Preliminary observations of complex object manipulation in a wild population of sapajus cay illiger 1815 (primates: cebidae) in a fragment of upper paraná atlantic forest, rancho laguna blanca, eastern paraguay. Acta Ethologica, 20(1), 75–80. https://doi.org/10.1007/s10211-016-0244-1