|White-nosed coati (Nasua narica)|
Nasua differs from Nasuella in being larger and having larger canine teeth, but preliminary genetic evidence (cytochrome b sequences) suggests that Nasuella should be merged into Nasua. Other genetic studies have shown that the closest relatives of the coatis are the olingos (genus Bassaricyon), from which they diverged about 10.2 million years ago.
Like other procyonids, coatis are omnivores. Their diet consists largely of insects (including their larvae), spiders and other invertebrates as well as the occasional small vertebrate discovered while energetically foraging, with their sensitive noses to the ground, in forest leaf litter. On Barro Colorado Island, Panama, where they have been studied in greatest detail, they supplement this diet with copious amounts of fruit as it becomes available seasonally from favored trees, such as figs (Ficus insipida) and hog plums (Spondias mombin).
Their very active foraging behavior appears to be interrelated with their distinctive social organization. Exceptional among procyonids, coatis are diurnal and for much of the year gregarious. Though females nest, and bear and nurse their young in isolation, shortly after the altricial young become mobile the females aggregate into social groups known as bands. Bands consist of adult females (two or more years old), and sub-adults (1–2 years old) and juveniles (less than 1 year old) of both sexes. At maturity, at two years of age, males are excluded from bands and take up a solitary lifestyle. They are aggressively repelled from bands, except during the mating season when typically one male ingratiates himself to a band through submissive behavior, forages with it for a period of a few weeks, and mates with all of the adult females. During the nesting season, the sub-adults and juveniles remain together in bands while breeding adult females become solitary for parturition and nesting. Females begin breeding in their 3rd or 4th year, apparently depending on nutritional status. Occasionally, older females become postreproductive, and these remain with the bands while breeding females separate. Breeding is synchronous, as is parturition and nursing. Resumption of gregarious behavior takes place synchronously as well, over the course of several weeks, depending on the existence of previous social relationships, i.e. females with prior relationships reaggregate into bands more quickly than those forming new relationships. Nonetheless, persistent social bonds may form anew at this point in the reproductive cycle: while there may be a tendency to reaggregate with kin, prior relationships are not indispensable. Previously unfamiliar individuals may aggregate into bands with stable social relationships. A conspicuous means of bond formation is mutual grooming, on which an hour or more may be spent daily. Some of this appears to be ritualized as a form of social bond formation (Fig. 1), though it is clearly mutually beneficial as well: the burden of ticks on band members is lower than it is on solitary adult males, for instance.
When juveniles descend from the nest, they are little better than helpless. One important benefit of aggregating for the adult females is sharing of vigilance in protection of juveniles from predation. Juvenile mortality is high, sources of peril including adult male coatis which have been observed to kill them. It is not entirely clear whether adult males are preying on them or killing potential rivals, and of course it may be both.
The active foraging behavior of coatis is fairly conspicuous, and requires a considerable degree of attention. The proportion of time that adult females spend foraging increases, and the proportion of foraging time interrupted for stationary vigilance behavior decreases, when aggregation into bands is achieved. Bands forage in formation, with adults and sub-adults distributed around the periphery, and juveniles gathered towards the center. This shared vigilance appears to be an important contributor to the benefit of gregariousness for coatis.
The two species within Nasua are:
|Image||Scientific name||Common Name||Distribution|
|N. narica (Linnaeus, 1766)||white-nosed coati, pizote, or antoon||Southwestern United States, Mexico, Central America, and northwest Colombia|
|N. nasua (Linnaeus, 1766)||South American coati||South America|
DNA sequence analysis indicates that the N. narica and N. nasua lineages split about 5.6 million years ago.
- "Mammal Species of the World". Archived from the original on 2008-03-16. Retrieved 2007-07-14.
- Emmons, Louise (1997). Neotropical Rainforest Mammals, A Field Guide (2nd ed.). Chicago: University of Chicago Press. pp. 153–154. ISBN 978-0-226-20721-6. OCLC 35686100.
- Helgen, K. M.; Kays, R.; Helgen, L. E.; Tsuchiya-Jerep, M. T. N.; Pinto, C. M.; Koepfli, K. P.; Eizirik, E.; Maldonado, J. E. (August 2009). "Taxonomic boundaries and geographic distributions revealed by an integrative systematic overview of the mountain coatis, Nasuella (Carnivora: Procyonidae)" (PDF). Small Carnivore Conservation. 41: 65–74. Archived from the original (PDF) on 2014-01-16. Retrieved 2013-08-20.
- K.-P. Koepfli; M. E. Gompper; E. Eizirik; C.-C. Ho; L. Linden; J. E. Maldonado; R. K. Wayne (2007). "Phylogeny of the Procyonidae (Mammalia: Carvnivora): Molecules, morphology and the Great American Interchange". Molecular Phylogenetics and Evolution. 43 (3): 1076–1095. CiteSeerX 10.1.1.495.2618. doi:10.1016/j.ympev.2006.10.003. PMID 17174109.
- Eizirik, E.; Murphy, W. J.; Koepfli, K.-P.; Johnson, W. E.; Dragoo, J. W.; Wayne, R. K.; O'Brien, S. J. (2010-02-04). "Pattern and timing of diversification of the mammalian order Carnivora inferred from multiple nuclear gene sequences". Molecular Phylogenetics and Evolution. 56 (1): 49–63. doi:10.1016/j.ympev.2010.01.033. PMID 20138220.
- Helgen, K. M.; Pinto, M.; Kays, R.; Helgen, L.; Tsuchiya, M.; Quinn, A.; Wilson, D.; Maldonado, J. (2013-08-15). "Taxonomic revision of the olingos (Bassaricyon), with description of a new species, the Olinguito". ZooKeys (324): 1–83. doi:10.3897/zookeys.324.5827. PMC 3760134. PMID 24003317.
- Patent, D.H. (1979). Raccoons, coatimundis and their family. Holiday House, New York
- Kaufmann, J.H. (1962). Ecology and social behavior of the coati, Nasua narica on Barro Colorado Island, Panama. Univ. of California Publications in Zoology 60:95-222.
- Russell, J.K. (1982). Timing of reproduction by coatis (Nasua narica) in relation to fluctuations in food resources. In: The Ecology of a Tropical Forest. Seasonal Rhythms and Long-term Changes. E.G. Leigh, Jr., A. S. Rand, D. M Windsor (eds). Smithsonian Inst. Press, Washington, D.C.
- Russell, J.K. (1983). Altruisim in coati bands: Nepotism or reciprocity? In: Wasser, S. (ed). Social Behavior of Female Vertebrates. Academic Press, New York
- Russell, J.K. (1981). "Exclusion of adult male coatis from social groups: Protection from predation". Journal of Mammalogy. 62 (1): 206–208. doi:10.2307/1380499. JSTOR 1380499.
- Kays, R. (2009). White-nosed Coati (Nasua narica), pp. 527-528 in: Wilson, D.E., and R.A. Mittermeier, eds. (2009). Handbook of the Mammals of the World. Vol. 1, Carnivores. ISBN 978-84-96553-49-1
- Decker, D.M. (1991). Systematics Of The Coatis, Genus Nasua (Mammalia, Procyonidae) Archived 2014-10-06 at the Wayback Machine. Proceedings of the Biological Society of Washington 104: 370-386
- Reid, Fiona A. (1997). A Field Guide to the Mammals of Central America and Southeast Mexico. pp. 259–260. ISBN 978-0-19-506400-1. OCLC 34633350.
- Samudio, R.; Kays, R.; Cuarón, A.D.; Pino, J.L. & Helgen, K. (2008). "Nasua narica". IUCN Red List of Threatened Species. Version 2008. International Union for Conservation of Nature. Retrieved 6 May 2012.