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Brief Summary ( Inglês )

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Norops auratus is a small, slender lizard with a brown base color and light yellow stripes along the body. It occurs almost exclusively in grasslands, and is found from northern South America to Panama.
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Size ( Inglês )

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Norops auratus is a small lizard, with a maximum snout-vent length of 57mm in females and 50mm in males. The head, which comprises approximately 25% of the SVL, is around 1.75 times longer than it is wide, with a pointed snout and flat or slightly depressed frontal region. The hind limbs of this species average .71 times the SVL, while the forelimbs are generally around .4 times the SVL. The tail has a round cross section and is slightly longer relative to the body in males, averaging 2.9 times SVL in males and 2.5 times SVL in females. The digits of this species end in expanded toepads covered in rows of structures called lamellae, each of which is covered in tiny hairs called setae. A weak adhesive interaction called Van der Waal’s force occurs between each setae and the substrate, which provide the adhesion necessary to climb vertical and overhanging surface. Generally there are 27 to 35 lamellae on the fourth toepad of individuals of this species. The scales covering the snout are keeled and asymmetrically polygonal. Generally one to two scales separate the supraorbital semicircles (rows of enlarged scales on the top of the head above the orbits) from each other, but in rare cases there can be no separation; the supraorbital semicircles are indistinct and comprised of keeled scales. Supraoccular scales (the scales directly below the supraorbital semicircles) are large, keeled, and asymmetrically polygonal medially; the rest of the supraoccular scales are small, keeled, and tend to be larger towards the front of the lizard. There are two parallel rows of supraciliary scales that run along the top margin of the eye, with the first scale of each row significantly longer than subsequent scales. The interparietal scale, which is medially located slightly posterior to the orbits, is several times the size of surrounding scales and is separated from the supraorbital semicircles by 1 to 3 scales. Below the orbits there are 3-5 keeled suboccular scales, which are either adjacent to or separated by 1 row of scales from the row of 5 to 8 keeled supralabial scales along the upper jaw margin. The scales located dorsally along the body are keeled, overlapping, and form 8 to 13 longitudinal rows; they are significantly larger than the scales along the flank but smaller than the ventral scales. Like other anoles, individuals of this species have a retractable flap of skin on the throat known as a “dewlap”. In males the dewlap is relatively small, reaching the forelimbs when extended; in females, it is all but non-existent. The body and head of this species is generally light brown to grayish brown, and is covered in small darker spots. There may be a brownish-yellow stripe along the back, and there is generally a yellow stripe along the flank. The ventral coloration is white on the head and speckled with brown along the body. The dewlap is blue and green in males, surrounded by pale yellow; in females, it may either have a blue patch or lack any contrasting coloration.
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Distribution ( Inglês )

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N. auratus is found from northern South America to southern Central America. There are populations along the Amazon and in the states of Roraima and Amapa in Brazil, in the coastal savannahs of French Guiana, in suitable habitat throughout Suriname, in Guyana, in Venezuela, along the Rio Cauca and Rio Magdalena valleys of Colombia , and in Panama.
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Trophic Strategy ( Inglês )

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This species has a sit-and-wait hunting strategy; its diet is composed almost entirely of insects and spiders.
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General Behavior ( Inglês )

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N. auratus is diurnal and heliothermic, and is often seen basking in sunny areas. The lizards are generally active between 7:30 and 18:30.
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General Habitat Information ( Inglês )

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Norops auratus is found in open areas; it is generally found in dense grass but may also be present in other low vegetation, tree trunks, and rock piles. In areas occupied by humans, they may be found in lawns, on fence posts, in gardens, or on walls, among other substrates.
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Habitat selection ( Inglês )

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Norops auratus utilize what is known as “post-vantage” behavior to orient themselves in their environment and aid in habitat selection. This entails climbing up onto perches that rise above the tall grass that characterizes N. auratus habitat in order to visually survey the surrounding area and select suitable habitats in the vicinity. This is likely an adaptation to overcome problems associated with the limited visibility in dense grass, which is generally only a few feet when perched on top of the grass and often only inches when within the grass (Keister et. al 1975).
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Post-Vantage behavior ( Inglês )

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Norops auratus utilize what is known as “post-vantage” behavior to orient themselves in their environment and aid in habitat selection. This entails climbing up onto perches that rise above the tall grass that characterizes N. auratus habitat in order to visually survey the surrounding area and select suitable habitats in the vicinity. This is likely an adaptation to overcome problems associated with the limited visibility in dense grass, which is generally only a few feet when perched on top of the grass and often only inches when within the grass (Kiester et. al 1975)
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Territoriality ( Inglês )

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Leo Fleishman observed that there are two distinct behavioral groups within adult male N. auratus. Members of one group are highly territorial and active, frequently adopting elevated perches to perform assertion and challenge displays that include head bobbing and dewlaping. Males within the other behavioral group lack such assertive displays, and are frequently observed within the territories of males in the first group; these non-territorial males generally are found close to the ground, often hidden under vegetation. Territorial males have mutually exclusive territories that they will defend against other territorial males; juveniles and females are tolerated within the territory, as are adult males if they give a head nod display (which is an acceptance of subordinate status) in response to the territorial male’s challenge display. If the intruding male does not respond or gives a challenge display to the territorial male, the intruding male is chased out of the territorial male’s territory or the two lizards engage in agonistic conflict that may include physical struggle. A male that loses such a contest may remain in the area, but adopts a subordinate status to the winner (Fleishman 1988).
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Thermal Ecology ( Inglês )

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N. auratus is diurnal and heliothermic, and is often seen basking in sunny areas. The lizards are generally active between 7:30 and 18:30; during this time, their body temperature is usually 32-36 degrees. The maximum temperature N. auratus will voluntarily reach without moving to a cooler area is 32.9±0.48°C. The critical thermal maximum, or the temperature at which these lizards are no longer able to move to a cooler area, is 40.0±0.38°C; temperatures around 41.1±0.33°C are lethal individuals of this species (Ballinger et. al 1970)
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Distribution ( Inglês )

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Continent: Middle-America
Distribution: Mexico (Oaxaca, Veracruz, Yucatan, Campeche, Quintana Roo), Belize, Guatemala, Honduras, Nicaragua, El Salvador; elevation: 80-940 m spilorhipis:
Type locality: Mexico: [Villa Allende,] Cerro Ombligo, Chiapas; HOLOTYPE: UIMNH 37972; M. Alvarez del Toro; March 20, 1954.
Type locality: œHuanuco [sic]; probably = Huatusco, Veracruz.
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Distribution ( Inglês )

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Continent: Middle-America South-America
Distribution: Costa Rica, Panama, Venezuela (Falcon, Cojedes), Colombia, Ecuador, French Guiana, Brazil (Amazonas)
Type locality: œTropical America, restricted to Surinam by SCHMIDT 1939.
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Anolis auratus ( Inglês )

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Anolis auratus, the grass anole, is a species of lizard in the family Dactyloidae. The species is found in Costa Rica, Panama, Venezuela, Colombia, French Guiana, Guyana, and Brazil.[2]

Description

Though A. auratus presents a variety of physical characteristics based on geographic location, maturity, and sex, it commonly displays a tan dorsal surface with cream or dark brown to black lateral stripes, copper orange spots on the posterior thigh, a bright orange tongue, as well as an overall tan tail with light gray or black streaks, blotches, or stripes on the dorsal surface but orange coloration underneath. The female has a smaller dewlap with gray to blue skin in between cream scales, while the male possesses a larger dewlap, similar in skin color to that of the female but with yellow scales at the center and base of the structure.[3]

In general, male and female A. auratus exhibit differences in pelvis width, trunk length, and head size, and thus, are sexually dimorphic with females possessing bigger pelvises and trunks and males having larger heads. As females play a more important role in reproduction, their larger trunks and wider pelvises allow them to carry more eggs as well as oviposit, or lay, heavier and bigger eggs respectively. On the other hand, males exhibit larger head dimensions than females, which may be attributable to their participation in male-to-male competitive interactions for female mates, resources, and/or territories. Predominantly used as a weapon during male-to-male combat, the head size plays a significant role in establishing dominance, territoriality, fitness, as well as mating success since a bigger head may be associated with greater jaw strength and thus, stronger bite force.[4]

Geographic range and habitat

A. auratus is widely distributed throughout Central America as well as northern regions of South America, extending from Costa Rica and spanning through much of Colombia, Venezuela, Brazil, Surinam, and the Guyanas.

Unlike other Anolis species, A. auratus inhabits moderately verdant grasslands rather than arboreal, or branchy, environments, which researchers presume may have given rise to its unique social organization. It prefers to live in fields, roadsides, or river edge marshes, and avoid shaded, brushy, as well as second growth regions. These grassy habitats are extremely short-lived, as they develop from some kind of disturbance to the area, like flooding, burning, or clearing by humans, and eventually become uninhabitable, growing into secondary forests. Hence, the grass anole doesn't occupy a single permanent territory throughout its lifetime; rather, it is continually on the move from habitat to habitat, relocating once its previous dwelling is destroyed by a disturbance or eliminated via natural processes. Moreover, vegetation is dense near the ground with long grass stalks sprouting out, which leaves any and all elevated perches in the area – primarily used by males for assertion displays – exposed. In addition, insolation is higher in grassy habitats than arboreal ones, suggesting that A. auratus has adapted to tolerate and ultimately favor higher temperatures.[5]

A. auratus is mainly found in Panama but can be found across northern South America in open, grassy areas such as fields. It tends to avoid shaded areas. [6]

Diet

Described as a sit-and-wait predator, A. auratus forages for its food by spending most of the day sitting and waiting for prey to pass. Its diet consists mainly of invertebrates, more specifically arthropods, including Hymenoptera, Hemiptera, Chilopoda, Araneae, Orthoptera, and larvae. Generally, it is known to be an opportunistic feeder, ingesting a wide variety of arthropods and selecting prey on the basis of size rather than species type or identity. Furthermore, the size of the grass anole significantly affects the size of its prey, as bigger lizards have larger mouths, to effectively consume more massive arthropods. Diet may also vary throughout the seasons.

Ecology and behavior

Territoriality

Males almost exclusively use their territories for access to mates rather than access to food since competition for food is low within the species. Males use displays to assert dominance over others males and attract females.[7] These displays consist of moving the head and dewlap up and down in a sinusoidal fashion.[7] A territorial male will approach another lizard to perform its display, and the sex and response of the conspecific will determine the result of the challenge. If the conspecific is female or a juvenile, it is tolerated within the male's territory. If the conspecific is another adult male, it is tolerated if it gives a head nod, but is chased away or engaged in agonistic behavior if it does not give a head nod or gives a challenge display. If the adult male conspecific loses the challenge, it can stay within the territory as a subordinate.[6]

Since A. auratus’ habitat has abundant vegetation, the effectiveness of head displays may be affected by the moving vegetation, especially in the wind. Displays can also be affected by the vantage point of females, which are usually low in the grass and become habituated to movement patterns in the moving vegetation. Therefore, displays are most successful when using a sinusoidal movement pattern when there is no wind, but even with wind, displays are able to generally avoid reduction in effectiveness from habituation.[7]

Social Behavior

The social system of A. auratus is described as that of a “tyrant-subordinate” system, in which there is one dominant territorial male with subordinate underlings occupying the same domain, and the latter group of lizards does not form dominance relationships amongst themselves. This social hierarchy has been observed and maintained during breeding seasons at natural population densities in the grass anole, rendering the behavior unique to this species, and many researchers attribute this phenomenon to the nature of the grassy habitat. Due to the transient formation and destruction of grasslands, subordinate males assume a higher net risk when challenging dominant males for territory ownership since the former must endure the high costs of fighting only to enjoy territorial dominion for a brief moment; thus, subordinates do not stand up against and engage in territorial battles with their dominants, as they will all have to relocate once their current grassy habitation becomes uninhabitable anyways. In accordance with this reasoning, dominant males also save energy by not forcing and driving out all the subordinate males from their territories, ultimately preserving the social organization. Furthermore, the exposed perches of these verdant lands make it difficult for subordinates to participate in displays for mating without getting caught by the dominant territory owners, leaving the subordinates no other choice but to comply. Consequently, the distinct “tyrant-subordinate” social system is maintained in A. auratus as a result of habitat demands.

Additionally, research studies show that individual A. auratus lizards prefer to associate with one another irrespective of size or sex. While in the absence of other conspecifics, they socialize with A. tropidogaster – a morphologically similar species. Previously, conspecific recognition was presumed to solely play a role in mate selection, aiding in reproductive isolation; however, the association of A. auratus with A. tropidogaster when conspecifics are not present as well as the tendency for same sex individuals to associate with one another suggest a purpose beyond reproductive selection. Accordingly, researchers attribute the attraction of conspecifics in the grass anole as a means of correct habitat selection, in which conspecifics are used as cues in deciding where one should settle in and occupy. The presence of conspecifics in a particular dwelling or environment may verify its suitability for livelihood in terms of resource availability and daily movements, in addition to potential for mates.

Adult Sociality

When given the choice of interacting with the same species or a morphologically similar species, A. auratus almost always chooses to interact with individuals of its own species. It only chooses to interact with other species when conspecifics are not around. This behavior suggests that being selective aids in reproductive isolation. It also suggests that being around conspecifics is important in habitat selection. [8]

Anolis auratus size comparison with a human finger
Grass anole observed in natural habitat

References

  1. ^ Ibáñez, R.; Jaramillo, C.; Köhler, G.; Rivas, G.; Gutiérrez-Cárdenas, P.; Bolívar, W.; Velasco, J.; Avila-Pires, T.C.S. (2020). "Anolis auratus". IUCN Red List of Threatened Species. 2020: e.T203078A2759962. doi:10.2305/IUCN.UK.2020-3.RLTS.T203078A2759962.en. Retrieved 19 November 2021.
  2. ^ "Anolis auratus ". The Reptile Database. http://reptile-database.reptarium.cz/species?genus=Anolis&species=auratus
  3. ^ Cole, Charles J.; Townsend, Carol R.; Reynolds, Robert P.; MacCulloch, Ross D.; Lathrop, Amy (January 2013). "Amphibians and reptiles of Guyana, South America: illustrated keys, annotated species accounts, and a biogeographic synopsis". Proceedings of the Biological Society of Washington. 125 (4): 317–578. doi:10.2988/0006-324X-125.4.317. ISSN 0006-324X. S2CID 86665287.
  4. ^ Acta Biológica Colombiana. Universidad Nacional de Colombia. 2014. doi:10.15446/abc.
  5. ^ Fleishman, Leo J. (1988). "The Social Behavior of Anolis auratus, a Grass Anole from Panama". Journal of Herpetology. 22 (1): 13–23. doi:10.2307/1564352. ISSN 0022-1511. JSTOR 1564352.
  6. ^ a b Fleishman, Leo J. (1988). "The Social Behavior of Anolis auratus, a Grass Anole from Panama". Journal of Herpetology. 22 (1): 13–23. doi:10.2307/1564352. JSTOR 1564352.
  7. ^ a b c Fleishman, Leo J. (1988-05-01). "Sensory and environmental influences on display form in Anolis auratus, a grass anole from Panama". Behavioral Ecology and Sociobiology. 22 (5): 309–316. doi:10.1007/BF00295099. ISSN 1432-0762. S2CID 33199717.
  8. ^ Kiester, A. Ross (1979-12-01). "Conspecifics as cues: A mechanism for habitat selection in the Panamanian grass anole (Anolis auratus)". Behavioral Ecology and Sociobiology. 5 (4): 323–330. doi:10.1007/BF00292522. ISSN 1432-0762. S2CID 40326441.
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Anolis auratus: Brief Summary ( Inglês )

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Anolis auratus, the grass anole, is a species of lizard in the family Dactyloidae. The species is found in Costa Rica, Panama, Venezuela, Colombia, French Guiana, Guyana, and Brazil.

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Norops auratus ( Basco )

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(RLQ=window.RLQ||[]).push(function(){mw.log.warn("Gadget "ErrefAurrebista" was not loaded. Please migrate it to use ResourceLoader. See u003Chttps://eu.wikipedia.org/wiki/Berezi:Gadgetaku003E.");});
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Norops auratus: Brief Summary ( Basco )

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Norops auratus Norops generoko animalia da. Narrastien barruko Dactyloidae familian sailkatuta dago.

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Anolis auratus ( Francês )

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Anolis auratus est une espèce de sauriens de la famille des Dactyloidae[1].

Répartition

Cette espèce se rencontre au Costa Rica, au Panama, en Colombie, en Équateur, au Venezuela, en Guyane et au Brésil au Pará et en Amazonas[1].

Taxinomie

Anolis auratus (O’Shaughnessy, 1869) nec Daudin, 1802 est un synonyme de Anolis tropidonotus Peters, 1863.

Publication originale

  • Daudin, 1802 : Histoire Naturelle, Générale et Particulière des Reptiles; ouvrage faisant suit à l'Histoire naturelle générale et particulière, composée par Leclerc de Buffon; et rédigee par C.S. Sonnini, membre de plusieurs sociétés savantes, vol. 4, F. Dufart, Paris, p. 1-397 (texte intégral).

Notes et références

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Anolis auratus: Brief Summary ( Francês )

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Anolis auratus est une espèce de sauriens de la famille des Dactyloidae.

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