Argentine black and white tegu#Blue tegu

{{short description|Species of lizard}}

{{Refimprove|date=March 2025}}

{{speciesbox

| image = Argentine Black and White Tegu (Salvator merianae) male - Flickr - berniedup.jpg

| image_caption = Male

| image2 = Black and White Tegu.jpg

| image2_caption = Female

| status = LC

| status_system = IUCN3.1

| status_ref = {{cite iucn |last1=Scott |first1=N. |last2=Pelegrin |first2=N. |last3=Montero |first3=R. |last4=Kacoliris |first4=F. |last5=Fitzgerald |first5=L. |last6=Carreira |first6=S. |last7=Cacciali |first7=P. |last8=Moravec |first8=J. |last9=Cisneros-Heredia |first9=D.F. |last10=Aparicio |first10=J. |last11=Avila-Pires |first11=T.C.S. |year=2016 |title=Salvator merianae |volume=2016 |page=e.T178340A61322552 |doi=10.2305/IUCN.UK.2016-1.RLTS.T178340A61322552.en |access-date=5 November 2021 }}

| status2 = CITES_A2

| status2_system = CITES

| status2_ref = {{Cite web|title=Appendices {{!}} CITES|url=https://cites.org/eng/app/appendices.php|access-date=2022-01-14|website=cites.org}}

| genus = Salvator

| species = merianae

| authority = A.M.C. Duméril & Bibron, 1839

| range_map = LagartoOvero.png

| synonyms = *Salvator merianae
{{small|A.M.C. Duméril & Bibron, 1839}}

  • Teius teguixim
    {{small|— Gray, 1845}}
  • Tupinambis teguixin
    {{small|— Boulenger, 1885}}
  • Tupinambis merianae
    {{small|— Dirksen & De la Riva, 1999}}
  • Salvator merianae
    {{small|— Harvey et al., 2012}}

| synonyms_ref = {{cite web|url=http://reptile-database.reptarium.cz/species?genus=Salvator&species=merianae |title=Tupinambis merianae|publisher=The Reptile Database |website=www.reptile-database.org}}

}}

The Argentine black and white tegu (Salvator merianae), also commonly known as the Argentine giant tegu, the black and white tegu, the blue tegu, and the huge tegu, is a species of lizards in the family Teiidae. The species is the largest of the "tegu" lizards.{{Cite web|url=http://www.wildherps.com/species/T.merianae.html|title=Wild Herps - Argentine Giant Tegu (Salvator merianae)|website=www.wildherps.com}} It is an omnivorous species, which inhabits the tropical rain forests, savannas, and semideserts of eastern and central South America. It is native to south and southeastern Brazil, Uruguay, eastern Paraguay, Bolivia, and Argentina.{{Cite journal |last1=Wood |first1=Jared P. |last2=Beer |first2=Stephanie Dowell |last3=Campbell |first3=Todd S. |last4=Page |first4=Robert B. |date=December 2018 |title=Insights into the introduction history and population genetic dynamics of the Argentine black-and-white tegu (Salvator merianae) in Florida |url=https://link.springer.com/10.1007/s10709-018-0040-0 |journal=Genetica |language=en |volume=146 |issue=6 |pages=443–459 |doi=10.1007/s10709-018-0040-0 |pmid=30244302 |issn=0016-6707|url-access=subscription }}

Tegu lizards are sometimes kept as pets, being notable for their unusually high intelligence and their ability to be housebroken. Like other reptiles, tegus go into brumation in autumn when the temperature drops. They exhibit a high level of activity during their wakeful period of the year. They are the only known nonavian reptiles to be partly endothermic.

Tegus fill ecological niches similar to those of monitor lizards, but are only distantly related to them; the similarities are an example of convergent evolution.

Taxonomy and etymology

The Argentine black and white tegu is in the order Squamata and the family Teiidae,{{Cite web |title=Teiidae {{!}} lizard family {{!}} Britannica |url=https://www.britannica.com/animal/Teiidae |access-date=2023-01-24 |website=www.britannica.com |language=en}} which also includes racerunners and whiptails. Nine genera of "tegus" (though new taxonomic classifications change) are known, with the Argentine black and white tegu being assigned to the genus Salvator.

The specific name, merianae, is in honor of German-born naturalist Maria Sibylla Merian,{{cite book|last1=Beolens|first1=Bo|author1-link=Bo Beolens|last2=Watkins|first2=Michael|author2-link=Michael Watkins (zoologist)|last3=Grayson|first3=Michael|author3-link=Michael Grayson|title=The Eponym Dictionary of Reptiles|date=2011|publisher=Johns Hopkins University Press|location=Baltimore|isbn=978-1-4214-0135-5}} xiii + 296 pp. (Tupinambis merianae, p. 175). a naturalist and artist who studied insects, plants, and reptiles from the 17th to the 18th centuries.{{Cite web|url=https://nmwa.org/art/artists/maria-sibylla-merian/|title=Maria Sibylla Merian | Artist Profile}}

Description

File:Black and white tegu.JPG

As a hatchling, S. merianae has an emerald-green color from the tip of its snout to midway down its neck, with black markings. The emerald green becomes black several months after shedding. As a young tegu, the tail is banded yellow and black; as it ages, the solid yellow bands nearest to the body change to areas of weak speckling. Fewer solid bands indicate an older animal. A tegu can drop a section of its tail as a distraction if attacked. The tail is also used as a weapon to swipe at an aggressor; even a half-hearted swipe can leave a bruise.{{citation needed|date=December 2021}} The tegu can live 12 to 15 years in the wild, though with exceptional care, they could survive more than 20 in captivity.{{Cite web |date=2025-06-02 |title=Argentine Black and White Tegu Care |url=https://petswithscales.com/argentine-black-and-white-tegu-care/}}

Tegus are capable of running at high speeds and can run bipedally for short distances. They often use this method in territorial defense, with their mouths open and front legs held wide to look more threatening.{{citation needed|date=December 2021}}

Adult males, much larger than the females, can reach {{convert|3|ft|cm|0|abbr=on}} in total length (tail included) at maturity. They may continue to grow to total lengths of {{convert|4-4.5|ft|cm|abbr=on}}.{{citation needed|date=December 2021}}

The females are much smaller, but may grow up to {{convert|3|ft|cm|abbr=on}} in length from nose to tail tip. Females have beaded skin and stripes running down the body. Adult females can reach a weight of {{convert|2.5-7.0|kg|lb|abbr=on}}.{{cite journal |last1=Basso |first1=C. P. |last2=Garriz |first2=C. |last3=Vieites |first3=C. M. |last4=Acerbi |first4=M. |last5=Perez Camargo |first5=G. M. |last6=Gonzalez |first6=O. M. |year=2004 |title=Rendimiento de canales de lagartos (Tupinambis merinae) criados en cautiverio |trans-title=Carcass yield of tegu lizard (Tupinambis merinae) raised in captivity |language=es |journal=Archivos de Zootecnia |volume=53 |issue=203 |pages=345–348 |url=http://www.uco.es/organiza/servicios/publica/az/php/img/web/17_12_32_15NotaRendimientoBasso.pdf |archive-url=https://web.archive.org/web/20131203033255/http://www.uco.es/organiza/servicios/publica/az/php/img/web/17_12_32_15NotaRendimientoBasso.pdf |archive-date=3 December 2013 }}

The skull is heavily built with a large facial process of the maxilla, a single premaxilla, paired nasals, a single frontal bone, and two parietal bones separated by the sagittal suture. Biomechanical analyses suggest the posterior processes of the parietal might be important for dealing with torsional loads due to posterior biting on one side.{{cite journal|vauthors=Jones ME, Gröning F, Dutel H, Fagan MJ, Evans SE|title=The biomechanical role of the chondrocranium and sutures in a lizard cranium |journal=Journal of the Royal Society Interface |year=2017 |volume=14 |issue=137 |page=20170637 |pmid=29263126 |doi=10.1098/rsif.2017.0637 |pmc=5746569 }} In the large adults, the posterior teeth are larger and more rounded than the anterior teeth.{{cite journal|author=Presch W|title=A survey of the dentition of the macroteiid lizards (Teiidae: Lacertilia) |journal=Herpetologica |year=1974 |volume=30 |issue=4 |pages=344–349|jstor=3891430}}

=Sex=

When a tegu reaches the age of 8 months, its sex can easily be determined visually. Its vent at the base of the tail bulges if it is a male, but lies flat if it is a female. Breeders generally inform the buyer of the sex of the animal before the purchase. In adults, the main difference is in the jowls. Males have substantially developed jowls as a result of hypertrophic lateral pterygoideus muscles.{{cite journal |last1=Rieppel |first1=Olivier |title=The trigeminal jaw adductor musculature of Tupinambis, with comments on the phylogenetic relationships of the Teiidae (Reptilia, Lacertilia) |journal=Zoological Journal of the Linnean Society |date=1980 |volume=69 |issue=1 |pages=1–29 |doi=10.1111/j.1096-3642.1980.tb01930.x|doi-access=free }} Females' jawlines are more streamlined.{{cn|date=December 2021}}

Ecology

=Distribution and habitat=

As one of its common names would suggest, S. merianae is native to Argentina, but also to Brazil, Paraguay, Bolivia, and Uruguay.{{ cite web | url=https://www.evergladescisma.org/the-dirty-dozen/tegu-lizards/ | title=Tegu Lizards - Everglades CISMA | date=21 September 2022 }}

Salvator merianae (once known as Tupinambis merianae) is a large reptile native to South America. Significant populations of Argentine black and white tegus occur in the southern United States and the Brazilian coast. They are a consistently problematic invasive species in Florida and Georgia, along with sightings in South Carolina,{{Cite journal |last1=Haro |first1=Daniel |last2=McBrayer |first2=Lance D. |last3=Jensen |first3=John B. |last4=Gillis |first4=James M. |last5=Bonewell |first5=Lea' R. |last6=Nafus |first6=Melia G. |last7=Greiman |first7=Stephen E. |last8=Reed |first8=Robert N. |last9=Yackel Adams |first9=Amy A. |date=2020-11-04 |title=Evidence for an Established Population of Tegu Lizards (Salvator merianae) in Southeastern Georgia, USA |url=https://bioone.org/journals/southeastern-naturalist/volume-19/issue-4/058.019.0404/Evidence-for-an-Established-Population-of-Tegu-Lizards-Salvator-merianae/10.1656/058.019.0404.full |journal=Southeastern Naturalist |volume=19 |issue=4 |doi=10.1656/058.019.0404 |issn=1528-7092|url-access=subscription }} most likely as a result of escaped or released specimens from the early-2000s pet trade. Previous studies have found that the differing weather and climate patterns far outside of their natural habitat range do not prevent adult Argentine black and white tegus from surviving in diverse areas across the United States, furthering concerns about their invasive status. In the wild, tegus inhabit both forested and open-plain environments, widening their potential invasive range.{{cite journal |last1=Goetz |first1=Scott M. |last2=Steen |first2=David A. |last3=Miller |first3=Melissa A. |last4=Guyer |first4=Craig |last5=Kottwitz |first5=Jack |last6=Roberts |first6=John F. |last7=Blankenship |first7=Emmett |last8=Pearson |first8=Phillip R. |last9=Warner |first9=Daniel A. |last10=Reed |first10=Robert N. |title=Argentine Black and White Tegu (Salvator merianae) can survive the winter under semi-natural conditions well beyond their current invasive range |journal=PLOS ONE |date=10 March 2021 |volume=16 |issue=3 |pages=e0245877 |doi=10.1371/journal.pone.0245877 |pmid=33690637 |pmc=7946314 |bibcode=2021PLoSO..1645877G |doi-access=free }} The first evidence of a reproducing population of these tegus into southeastern Florida occurred when a female was tracked to her nest mound. One clutch of 21 eggs from the current year was found and one clutch of 22 hatched eggshells and 13 unhatched eggs was found from a past year. Established communities were identified in Hillsborough and Polk Counties in Florida.{{Cite journal |last1=Pernas |first1=Tony |last2=Giardina |first2=Dennis J. |last3=McKinley |first3=Alan |last4=Parns |first4=Aaron |last5=Mazzotti |first5=Frank J. |date=2012 |title=First Observations of Nesting by the Argentine Black and White Tegu, Tupinambis merianae, in South Florida |url=https://www.jstor.org/stable/41819793 |journal=Southeastern Naturalist |volume=11 |issue=4 |pages=765–770 |doi=10.1656/058.011.0414 |jstor=41819793 |issn=1528-7092|url-access=subscription }}

Tegus have also been found in scrub and wet habitats such as flooded savannas, canals, ponds, and streams. They largely seem to not discriminate in habitat type as long as they have the ability to burrow.{{cite journal |last1=Pernas |first1=Tony |last2=Giardina |first2=Dennis J. |last3=McKinley |first3=Alan |last4=Parns |first4=Aaron |last5=Mazzotti |first5=Frank J. |title=First Observations of Nesting by the Argentine Black and White Tegu, Tupinambis merianae, in South Florida |journal=Southeastern Naturalist |date=December 2012 |volume=11 |issue=4 |pages=765–770 |doi=10.1656/058.011.0414 |s2cid=86304661 }}

=Diet=

Tegus are omnivorous; juveniles in the wild have been observed to eat a wide range of invertebrates, including insects, annelids, crustaceans,{{cite web |last1=Kiefer |first1=Mara Cíntia |last2=Sazima |first2=Ivan |title=Diet of juvenile tegu lizard Tupinambis merianae (Teiidae) |pages=105–108 |url=https://ecoevo.com.br/publicacoes/pesquisadores/ivan_sazima/2002_dietofjuveniletegulizarTupinambismerianae.pdf }} in {{cite journal |title=Short Notes |journal=Amphibia-Reptilia |date=1 January 2002 |volume=23 |issue=1 |pages=93–124 |doi=10.1163/156853802320877654 }} spiders, and snails.{{cite journal |last1=Colli |first1=Guarino R. |last2=Péres |first2=Ayrton K. |last3=Cunha |first3=Hélio J. da |title=A New Species of Tupinambis (Squamata: Teiidae) from Central Brazil, with an Analysis of Morphological and Genetic Variation in the Genus |journal=Herpetologica |date=1998 |volume=54 |issue=4 |pages=477–492 |jstor=3893442 }} They also eat fruits and seeds. As they mature, their diet becomes more generalized, and plant consumption increases. They may seek out eggs from the nests of birds and other reptiles, and eat small birds and other vertebrates such as fish, frogs, other lizards, snakes, and small mammals (such as rodents). They can also hunt larger prey, such as armadillos.{{citation needed|date=August 2023}} Adults continue to eat insects and wild fruits, and such components are assumed to include desirable or essential nutrients.

In captivity, tegus commonly are fed high-protein diets that include raw or cooked flesh, such as ground turkey, canned or dry dog food, commercial crocodile diet, chicken, eggs, insects, and small rodents. The inclusion of fruit in the diet is recommended. Though some captive tegus do not readily eat fruit, others readily consume bananas, grapes, mangoes, and papayas. However, some evidence indicates that cooking most of the egg in the diet is a good practice, so as to denature the protein avidin that occurs in the albumen. Raw avidin immobilises biotin, so excessive feeding of raw eggs may cause fatal biotin deficiency.{{cite book|author=Hoff, Gerald|title=Diseases of Amphibians and Reptiles|url=https://books.google.com/books?id=w1PxBwAAQBAJ&pg=PA643|date=6 December 2012|publisher=Springer Science & Business Media|isbn=978-1-4615-9391-1|pages=643–}}

As adults, they have blunted teeth and exaggerated lateral pterygoid muscles, which allow them to be generalist feeders. In captivity, they have been observed eating various feeder insects, such as mealworms, superworms, earthworms, silkworms, crickets, and cockroaches, as well as vertebrate prey, including mice, rats, fish, turkey (offered in a ground form), rabbit, quail, and chicken chicks. Crustaceans such as crayfish are also readily consumed. Like all lizards, these tegus need a properly balanced diet; incomplete prey items such as insects or ground meat require dusting with a mineral/multivitamin supplement. Vitamin deficiencies can lead to trouble shedding skin, lethargy, and weight loss; a calcium deficiency can lead to metabolic bone disease, which can be fatal.{{cite web|url=http://www.grizzlyrun.com/Pets/Reptiles/Lizards/Tegus/Default.htm |title=Tegus Directory |access-date=2009-01-08 |archive-url=https://web.archive.org/web/20090108093936/http://www.grizzlyrun.com/Pets/Reptiles/Lizards/Tegus/Default.htm |archive-date=2009-01-08 }}

Tegus are notorious egg predators, which increasingly makes them a concerning predator of sea turtles, alligators, and crocodiles as their invasive populations spread across the United States.

Tegus eat a range of foods from plants to hatchlings, but their diet varies by season. Small vertebrate prey is more common in the spring, while plants and invertebrates are more commonly consumed in the summer.{{cite journal |last1=Offner |first1=Marie-Therese |last2=Campbell |first2=Todd S. |last3=Johnson |first3=Steve A. |title=Diet of the Invasive Argentine Black and White Tegu in Central Florida |journal=Southeastern Naturalist |date=June 2021 |volume=20 |issue=2 |doi=10.1656/058.020.0210 |s2cid=236288920 }}

=Mortality=

Predators of tegus include cougars, jaguars, otters, snakes, caimans, and birds of prey. A known predator of the Argentine black and white tegu is the lesser grison (Galictis cuja), a mustelid related to weasels.{{cite journal |last1=Braga |first1=Caryne |last2=de Oliveira Drummond |first2=Leandro |last3=Dawn Henry |first3=Malinda |last4=Azevedo Khaled |first4=Fábio |last5=Rojas Arias |first5=Juan D. |last6=Ruiz-Miranda |first6=Carlos R. |last7=Rodrigues Gonçalves |first7=Pablo |title=Predation of the black-and-white tegu (Salvator merianae) by the lesser grison (Galictis cuja) |journal=Mastozoología Neotropical |date=July 2020 |volume=27 |issue=1 |pages=182–186 |doi=10.31687/saremMN.20.27.1.0.22 |s2cid=225635805 |doi-access=free }} Salmonella enterica was found in fecal samples from almost all S. merianae at a captive-breeding field station at State University of Santa Cruz, Ilhéus, Bahia, Brazil illustrating the prevalence of Salmonella infection in tegus.

Life cycle

Eggs of the Argentine black and white tegu usually hatch at the beginning of spring. Each hatchling weighs about {{cvt|10|g|oz|abbr=on}} and grows to {{cvt|8|kg|lb|abbr=on}} within four or five years, experiencing a nearly 800-fold increase in body size. During this time, its diet changes from insects to small vertebrates, eggs, carrion, and fruits. It is reproductively mature by its third year, when it weighs around {{cvt|1.5|kg|lb|abbr=on}}, and ceases growing by around its fourth year, with the highest growth rate being its first and second years of life. S. merianae also experiences a seasonal lifecycle that begins within its first year, being very active during hotter months and in a brumation state in the colder months. Regardless of the season, the Argentine tegu does not experience any significant fluctuations in metabolism or body mass, which means its sensitivity to temperature underlying its metabolic rate does not change body mass. This differs from other endotherms and further explains the tegu's alternating endothermic and ectothermic behavior.{{cite journal |last1=Toledo |first1=Luís F. |last2=Brito |first2=Simone P. |last3=Milsom |first3=William K. |last4=Abe |first4=Augusto S. |last5=Andrade |first5=Denis V. |title=Effects of Season, Temperature, and Body Mass on the Standard Metabolic Rate of Tegu Lizards ( Tupinambis merianae ) |journal=Physiological and Biochemical Zoology |date=March 2008 |volume=81 |issue=2 |pages=158–164 |doi=10.1086/524147 |pmid=18190282 |hdl=11449/21152 |s2cid=14258317 |hdl-access=free }}

Brain vesicles (constructed from two neural tube constrictions) that make up the anterior forebrain, midbrain, and posterior hindbrain are developed and distinguishable from day three of embryonic development. On day four, visceral arches (consisting of mesenchymal tissue condensation and separated by grooves) form and are fully grown and fused by day nine. Day four also marks the development of limbs as small swellings. Its hindlimb development (developing claws faster than the forelimb) is more similar to crocodile or turtle embryonic development than other lizards. This alludes to the hindlimbs having greater functionality in tegu adults. Pigmentation is the last morphological structure to form and occurs late in development after other distinguishing characteristics have already been formed (such as scales). Pigmentation is observed from day 39 first on the dorsal portion of the head and body. It later extends down to the proximal and distal portions of the limbs by day 45 and extends down to the flanks by day 48. As development advances, the pattern begins to show lateral stretch marks by day 51. Pigmentation of the ventral portion of the body occurs between days 57 and 60, characterized by individualized spot patterns. Paired genital tubercles manifest in both sexes (called hemipenes in males). Reptile embryo development involves separate processes of differentiation and embryo growth. Differentiation is determined by external morphological features and is documented early. As the embryo approaches hatching, development stages are categorized into periods rather than ages (characterized by parameters of development speed).{{cite journal |last1=Iungman |first1=Josefina L. |last2=Molinero |first2=María N. |last3=Simoncini |first3=Melina S. |last4=Piña |first4=Carlos I. |title=Embryological development of Salvator merianae (Squamata: Teiidae) |journal=Genesis |date=April 2019 |volume=57 |issue=4 |pages=e23280 |doi=10.1002/dvg.23280 |pmid=30620139 |s2cid=58636676 }}

Behavior

=Aggression=

Aggression is a vital facet to animal behavior, as it provides advantages to survival when resources are limited. For the Argentine tegu, the physical performance of its aggressive behavior (i.e. biting) tends to be hindered by its large size. Regardless of sex, tegus with higher bite force are more aggressive to potential threats. Those with a higher bite force also exhibit fewer escape responses and tend to be slower, displaying a tradeoff of fight or flight abilities, but also have the advantage of minimizing risk of energy by reducing the threshold for engagement in an aggressive encounter. This fight or flight tradeoff is more commonly observed in mammals rather than reptiles, and may be present in tegus because of an increase in head mass (correlated to stronger biting behavior) that makes maneuvering quickly difficult. In their home territories, Argentine tegus are generally less aggressive (less likely to display arching behavior) and are less likely to attempt escape regardless of size or bite force.{{cite journal |last1=Herrel |first1=Anthony |last2=Andrade |first2=Denis V. |last3=de Carvalho |first3=José Eduardo |last4=Brito |first4=Ananda |last5=Abe |first5=Augusto |last6=Navas |first6=Carlos |title=Aggressive Behavior and Performance in the Tegu Lizard Tupinambis merianae |journal=Physiological and Biochemical Zoology |date=November 2009 |volume=82 |issue=6 |pages=680–685 |doi=10.1086/605935 |pmid=19758090 |hdl=11449/21155 |s2cid=1982447 |hdl-access=free }}

=Reproduction=

Squamate reptiles such as snakes and lizards tend to rely on chemical cues to search for potential mates in their environments. A study using skin lipids indicates chemical cues can be used to modify movements of invasive reptiles in their non-native range, which could be useful in management strategies.{{Cite journal |last1=Parker |first1=M. Rockwell |last2=Tillman |first2=Eric A. |last3=Nazarian |first3=Lauren A. |last4=Barlowe |first4=Megan L. |last5=Lincoln |first5=Julianna M. |last6=Kluever |first6=Bryan M. |date=2023-10-31 |title=Skin lipids alone enable conspecific tracking in an invasive reptile, the Argentine black and white tegu lizard (Salvator merianae) |journal=PLOS ONE |volume=18 |issue=10 |pages=e0293591 |doi=10.1371/journal.pone.0293591 |doi-access=free |pmid=37906547 |pmc=10617720 |bibcode=2023PLoSO..1893591P |issn=1932-6203}} The Argentine black and white tegu exhibits similar behavior, such as a marked "pausing and turning" as they trail in the spring. In particular, female tegus exhibit stronger trailing behavior than males, following scent trails more intensely and expressing a more sensitive response to mating-specific chemical odors. They also exhibit more decisive behavior, demonstrating a common vertebrate trend of female reproduction being the defining factor in influencing population size. Knowledge of this behavior is currently being explored as a strategic avenue to inhibit the current rise of the tegu as an invasive species. Prioritizing the removal of female tegus from the environment can potentially be a more effective way to curb these invasive populations. Tegus are a burrowing species in both their native and invaded habitats, especially during the winter. They mate during the spring after hibernating when their mating hormones are at their peak. During the spring, male Argentine tegus exhibit scent-marking behaviors such as delineating territory with gland scents.{{cite journal |last1=Richard |first1=Shannon A. |last2=Bukovich |first2=Isabella M. G. |last3=Tillman |first3=Eric A. |last4=Jayamohan |first4=Sanjiv |last5=Humphrey |first5=John S. |last6=Carrington |first6=Paige E. |last7=Bruce |first7=William E. |last8=Kluever |first8=Bryan M. |last9=Avery |first9=Michael L. |last10=Parker |first10=M. Rockwell |title=Conspecific chemical cues facilitate mate trailing by invasive Argentine black and white tegus |journal=PLOS ONE |date=12 August 2020 |volume=15 |issue=8 |pages=e0236660 |doi=10.1371/journal.pone.0236660 |pmid=32785239 |pmc=7423067 |bibcode=2020PLoSO..1536660R |doi-access=free }}

Blue tegus, like other tegus, may breed up to twice a year. They lay between 18 and 25 eggs in a clutch, sometimes more, dependent upon animal size and husbandry, as well as the individual health of the gravid female.{{citation needed|date=December 2021}}

During maternal seasons, female Argentine black and white tegus build nests out of dry grass, small branches, and leaves to maintain optimal temperature and humidity levels. Egg incubation lasts for an average of 64 days, with a range of 40 to 75 days depending on incubation temperature and other extenuating factors.

Physiology

=Invasive advantage=

Physiologically, tegus possess traits that correlate well with their extreme success as an invasive species. Notably, they mature early, reproduce annually, have large clutch sizes, and a relatively long lifespan compared to other competing species. Of the Teiidae family, tegus tend to grow to the largest body sizes (around 5 kg). Tegus are also omnivorous and consume foods ranging from fruits, invertebrates, and small vertebrates to eggs and carrion. Their large dietary range also contributes to their high survival rate outside of their native habitat. Tegus are active on a seasonal schedule. They avoid dangerously cold or dry climates by hibernating underground. Additionally, they are capable of using endothermy to elevate their body temperatures in response to their environment.

=Endothermic behavior=

Tegus in their native environment spend most of the colder months brumating in their burrows without feeding, but emerge in the spring for their mating season. While brumating, their metabolism generates heat that maintains their temperature a few degrees above the burrow temperature, marking them as partial endotherms. This self-reliant endothermic behavior continues into the reproductive season. However, Argentine tegus only display this behavior for part of the year and behave as ectotherms for the rest (sunbathing, temperature reliant on environment). This endothermic behavior is also not a sex-biased evolutionary adaptation for egg production, as both males and females indiscriminately exhibit this behavior.{{cite journal |last1=Tattersall |first1=Glenn J. |last2=Leite |first2=Cleo A. C. |last3=Sanders |first3=Colin E. |last4=Cadena |first4=Viviana |last5=Andrade |first5=Denis V. |last6=Abe |first6=Augusto S. |last7=Milsom |first7=William K. |title=Seasonal reproductive endothermy in tegu lizards |journal=Science Advances |date=22 January 2016 |volume=2 |issue=1 |pages=e1500951 |doi=10.1126/sciadv.1500951 |pmid=26844295 |pmc=4737272 |bibcode=2016SciA....2E0951T}}

  • {{cite web |author=Peter Moon |date=February 24, 2016 |title=Giant tegu lizard is warm-blooded, researchers discover |website=Agência FAPESP |url=https://agencia.fapesp.br/giant-tegu-lizard-is-warm-blooded-researchers-discover/22723/}}

The Argentine tegu experiences significant shifts in metabolism and body temperature by season. They are highly active throughout the day during warmer months (such as participating in reproductive endothermy during the spring) and experience drastic metabolic suppression during the winter.{{cite journal |last1=Zena |first1=Lucas A. |last2=Dillon |first2=Danielle |last3=Hunt |first3=Kathleen E. |last4=Navas |first4=Carlos A. |last5=Buck |first5=C. Loren |last6=Bícego |first6=Kênia C. |title=Hormonal correlates of the annual cycle of activity and body temperature in the South-American tegu lizard (Salvator merianae) |journal=General and Comparative Endocrinology |date=1 January 2020 |volume=285 |page=113295 |doi=10.1016/j.ygcen.2019.113295 |pmid=31580883 |s2cid=203661361 |hdl=11449/196440 |hdl-access=free }}

Salvator merianae has recently been shown to be one of the few partially warm-blooded lizards, having a temperature up to {{convert|10|C-change}} higher than the ambient temperature at nighttime;{{cite journal |last1=Tattersall |first1=Glenn J. |last2=Leite |first2=Cleo A. C. |last3=Sanders |first3=Colin E. |last4=Cadena |first4=Viviana |last5=Andrade |first5=Denis V. |last6=Abe |first6=Augusto S. |last7=Milsom |first7=William K. |title=Seasonal reproductive endothermy in tegu lizards |journal=Science Advances |date=22 January 2016 |volume=2 |issue=1 |pages=e1500951 |doi=10.1126/sciadv.1500951 |pmid=26844295 |pmc=4737272 |bibcode=2016SciA....2E0951T }} however, unlike true endotherms such as mammals and birds, these lizards only display temperature control during their reproductive season (September to December), so are said to possess seasonal reproductive endothermy. Because convergent evolution is one of the strongest lines of evidence for the adaptive significance of a trait, the discovery of reproductive endothermy in this lizard not only complements the long known reproductive endothermy observed in some species of pythons,{{cite journal |last1=Hutchison |first1=Victor H. |last2=Dowling |first2=Herndon G. |last3=Vinegar |first3=Allen |title=Thermoregulation in a Brooding Female Indian Python, Python molurus bivittatus |journal=Science |date=11 February 1966 |volume=151 |issue=3711 |pages=694–696 |doi=10.1126/science.151.3711.694 |pmid=5908075 |bibcode=1966Sci...151..694H |s2cid=45839432 }} but also supports the hypothesis that the initial selective benefit for endothermy in birds and mammals was reproductive.{{cite journal |last1=Farmer |first1=C. G. |title=Parental Care: The Key to Understanding Endothermy and Other Convergent Features in Birds and Mammals |journal=The American Naturalist |date=March 2000 |volume=155 |issue=3 |pages=326–334 |doi=10.1086/303323 |pmid=10718729 |s2cid=17932602 }}{{cite journal |last1=Farmer |first1=C. G. |title=Reproduction: The Adaptive Significance of Endothermy |journal=The American Naturalist |date=December 2003 |volume=162 |issue=6 |pages=826–840 |doi=10.1086/380922 |pmid=14737720 |s2cid=15356891 }}

=Locomotion=

The Argentine black and white tegu is used to study the evolutionary history of shoulder joint locomotive muscles. Because of its weight and heavy girth, it has unique modifications to its skeletal gait that help map the evolutionary history of the nonmammalian musculoskeletal structure.{{cite journal |last1=Fahn-Lai |first1=Philip |last2=Biewener |first2=Andrew A. |last3=Pierce |first3=Stephanie E. |title=Broad similarities in shoulder muscle architecture and organization across two amniotes: implications for reconstructing non-mammalian synapsids |journal=PeerJ |date=18 February 2020 |volume=8 |pages=e8556 |doi=10.7717/peerj.8556 |pmid=32117627 |pmc=7034385 |doi-access=free }}

Interactions with humans and livestock

=As household pets=

==Blue tegu==

File:Blueteguspiral.jpg

The blue tegu is a variant known for its light blue coloration, which is most intense and vivid in the adult males. Even immature animals can be easily distinguished from other tegus – mostly black and white – by the "singe mark" on their noses. They are among the more suitable tegus for pets and can be easily tamed, but in the wild, they either try to run away or react aggressively if provoked.

The scientific classification of the blue tegu is contentious. Large-scale taxon sampling of the teiids has not led to any strong resolutions based on morphological and genetic data;{{cite journal |last1 = Pyron |first1 = R. |last2 = Burbrink |first2 = Frank T. |last3 = Wiens |first3 = John J. |year = 2013 |title = A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes |journal = BMC Evolutionary Biology |volume = 13 |issue = 1 |page = 93 |doi = 10.1186/1471-2148-13-93 |pmid = 23627680 |pmc = 3682911 |bibcode = 2013BMCEE..13...93P |doi-access = free }} the majority of data about the blue tegu comes from hobbyists. Some believe it is a mutation of the Argentine black and white tegu, while others, including the original importer, believe it is sufficiently different to classified as its own species, or a subspecies. The first blue tegu to be exported from South America was in a wholesale shipment of tegus from Colombia.{{cite web |title=Blue tegus (Tupinambis teguixin spp.) |url=http://www.bluetegu.com/blue.html |access-date=2020-09-03 |url-status=bot: unknown |archive-url=https://web.archive.org/web/20021207223247/http://www.bluetegu.com/blue.html |archive-date=2002-12-07}}

The coloring of a "blue" tegu can range from a simple black and white color, to albino, to powder blue, to even platinum (which is basically a high white color morph). The distinct colouration does not tend to appear until the animal reaches sexual maturity, around the age of 18 months or it reaches {{convert|2|ft|cm|0|abbr=on}} or more in size. Just like the Argentine black and white tegu, the blue tegu has a very quick growth rate, almost reaching 75% of its full length in 1 year. Their adult length can vary from {{convert|2.5|ft|cm|0|abbr=on}}, in adult females, to sometimes even longer than {{convert|4|ft|cm|0|abbr=on}} in adult males. Unlike many other lizards, tegus are very heavily built animals, ranging from {{convert|7|to|12|lb|kg|abbr=on}} or more when fully grown. Size varies due to genetics, husbandry (if any), and diet.{{cite web |title=Blue tegu – information and care |website=Pets with Scales |date=8 July 2022 |url=https://petswithscales.com/blue-tegu/ |access-date=12 July 2022}}

==Legality==

On May 28, 2021 the South Carolina Department of Natural Resources banned their importation and breeding, and requires registration of black and white tegus already in South Carolina.{{cite web | title=New regulations will ban tegus, require current owners to register reptiles | website=South Carolina Department of Natural Resources | date=2021-05-28 | url=https://www.dnr.sc.gov/news/2021/may/may28-tegu.php | access-date=2021-07-15}}{{cite web | last=Cheatam | first=Kristen | title=Invasive lizard species banned from South Carolina | website=WSPA-TV 7News | date=2021-06-02 | url=http://www.wspa.com/news/invasive-lizard-species-banned-from-south-carolina/ | access-date=2021-07-15}}

= As food =

S. merianae – like other animals used for bushmeat – is a common food source for humans in its native range. It could be an economically and dietarily beneficial meat source if used more widely.

=Leather trade=

Argentine black and white tegus have long been hunted for their skins to supply the international leather trade. They are one of the most exploited reptile species in the world, but trade is legal in most South American countries. It is not an endangered species and overharvesting has not as of yet been observed.{{cite thesis |last1=Romero |first1=Mieres |last2=Margarita |first2=Maria |title=Monitoring and managing the harvest of tegu lizards in Paraguay |date=2002 |hdl=1969.1/ETD-TAMU-2002-THESIS-M54 |hdl-access=free }}

Invasive species

In Florida, Argentine black and white tegus have escaped from the pet trade and are now an invasive species in Florida,{{cite web |title=Argentine Black and White Tegu |website=FWC |url=http://myfwc.com/wildlifehabitats/profiles/reptiles/argentine-black-and-white-tegu/}}{{cite web |title=Control of invasive tegus in Florida |department=Argentine black and white tegus |series=The Croc Docs |place=Ft. Lauderdale, FL |publisher=U. Florida |url=https://crocdoc.ifas.ufl.edu/projects/Argentineblackandwhitetegus/ }} Georgia{{cite web |title=Tegus |date=20 January 2021 |publisher=Georgia Invasive Species Task Force |url=http://www.gainvasives.org/tegus/}}{{cite web |title=Argentine black and white tegus |website=georgiawildlife.com |publisher=Georgia Department of Natural Resources, Wildlife Division |url=https://georgiawildlife.com/tegus}} and South Carolina.{{cite press release |title=First sighting of black and white tegu lizard confirmed in midlands |date=21 August 2020 |publisher=South Carolina Department of Natural Resources |url=https://www.dnr.sc.gov/news/2020/aug/aug_21.php}}{{cite news |title=Invasive tegu lizard spotted in Berkeley County, DNR monitoring |date=20 September 2020 |newspaper=Charleston City Paper |url=https://www.charlestoncitypaper.com/story/invasive-tegu-lizard-spotted-in-berkeley-county-dnr-monitoring}} The first sighting of S. merianae in Berkeley County, South Carolina was on 10 September 2020. Eight total sightings in South Carolina had been recorded as of 10 September 2020.

The Argentine black and white tegu has been a particular threat to native birds and reptiles that build nests or burrows on the ground. Notably, they exhibit a particular type of both predatory and competitive behavior known as intraguild predation, which worsens their invasive effect on wildlife; Argentine tegus will pursue and kill – but not eat – other native reptiles. Efforts such as placing traps or local hunting have been largely unsuccessful in reducing their bad effects in the non-native environments.

Because of their invasive threat to native and imperiled species, population containment initiatives have been a priority in the past 10 years, leading to the extraction of nearly 3,300 tegus from Miami-Dade County alone. Unfortunately tegu culling efforts have had little effect: Historically, tegus survived brutal leather-trade harvests in their native environment, demonstrating that they are a remarkably resilient species.

As of 29 April 2021, residents of Florida are now legally allowed to kill these invasive Argentine black and white tegus that are spotted on private property, with the landowners' permission, and on the public lands of Florida. Legal barriers that had been protecting the non-native reptiles have been removed, to prevent the population of tegus from increasing in Florida. As an alternative to killing them, the Florida Fish and Wildlife Conservation Commission staff offers to take control and maintain this species by capturing and removing tegus from the environment.{{cite web |title=Argentine black and white tegu |type=profile |publisher=Florida Fish and Wildlife Conservation Commission |url=https://myfwc.com/wildlifehabitats/profiles/reptiles/argentine-black-and-white-tegu/ |access-date=2023-03-07 |lang=en}}

Taxonomy

File:20110721 Berkenhof Zoo (0050).jpgs between the eye and nostril of this Argentine black and white tegu, plus its round pupils, identify it as belonging to the genus Salvator.]]

In 1839, this species of tegu was originally described as Salvator merianae. However, beginning in 1845 and continuing for 154 years, it was confused with Tupinambis teguixin and was considered a synonym of that species. In 1995, it was again given species status, as Tupinambis merianae because subsequent studies had shown that the gold tegu (Tupinambis teguixin) was distinct from it. In 2012, the Argentine black and white tegu was reassigned to the resurrected genus Salvator as Salvator merianae.{{cite journal |last1=Harvey |first1=Michael B. |last2=Ugueto |first2=Gabriel N. |last3=Gutberlet |first3=Ronald L. Jr |title=Review of teiid morphology with a revised taxonomy and phylogeny of the Teiidae (Lepidosauria: Squamata) |journal=Zootaxa |date=2012 |volume=3459 |issue=1 |pages=1–156 |doi=10.11646/zootaxa.3459.1.1 }}

S. merianae is called the "Argentine black and white tegu" to distinguish it from the "Colombian black and white tegu", which is another name for the gold tegu. Unscrupulous or incompetent pet dealers sometimes pass off gold tegus as Argentine black and white tegus.{{citation needed|date=December 2021}}

S. merianae and T. teguixin can be distinguished by skin texture and scale count:

  • S. merianae has two loreal scales between the eye and the nostril.
  • T. teguixin has only one loreal scale between the eye and the nostril.

In the ecotone between the arid Chaco and the Espinal of central Argentina, they are known to naturally hybridise with the red tegu (Salvator rufescens) with a stable hybrid zone.{{cite journal |last1=Cabaña |first1=Imanol |last2=Chiaraviglio |first2=Margarita |last3=Di Cola |first3=Valeria |last4=Guisan |first4=Antoine |last5=Broennimann |first5=Olivier |last6=Gardenal |first6=Cristina N |last7=Rivera |first7=Paula C |title=Hybridization and hybrid zone stability between two lizards explained by population genetics and niche quantification |journal=Zoological Journal of the Linnean Society |date=1 October 2020 |volume=190 |issue=2 |pages=757–769 |doi=10.1093/zoolinnean/zlaa018 |doi-access=free |hdl=11336/141610 |hdl-access=free }}

See also

==References==

{{reflist|refs=

{{cite book|vauthors=Duméril AM, Bibron G |title=Erpétologie générale ou Histoire naturelle complète des reptiles|date=1839|publisher=Roret|location=Paris|pages=85–90|chapter-url=https://www.biodiversitylibrary.org/page/32521238|chapter=Le sauvegarde de Mérian, Salvator Merianæ, Nobis|volume=5|doi=10.5962/bhl.title.87584 }}

{{cite web | title=Invasive Tegu Lizards Are Eating Their Way Through Southeastern US | website=WBUR-FM | date=2020-12-03 | url=https://www.wbur.org/hereandnow/2020/12/03/invasive-tegu-lizards | language=en | access-date=2020-12-06}}

{{cite journal |last1=Maciel |first1=B. M. |last2=Argôlo Filho |first2=R. C. |last3=Nogueira |first3=S. S. C. |last4=Dias |first4=J. C. T. |last5=Rezende |first5=R. P. |title=High Prevalence of Salmonella in Tegu Lizards (Tupinambis merianae), and Susceptibility of the Serotypes to Antibiotics: Prevalence of Salmonella in Tegus |journal=Zoonoses and Public Health |date=December 2010 |volume=57 |issue=7–8 |pages=e26–e32 |doi=10.1111/j.1863-2378.2009.01283.x |pmid=19968856 |s2cid=27434339 }}

{{cite journal |last1=Saadoun |first1=A. |last2=Cabrera |first2=M.C. |title=A review of the nutritional content and technological parameters of indigenous sources of meat in South America |journal=Meat Science |date=November 2008 |volume=80 |issue=3 |pages=570–581 |doi=10.1016/j.meatsci.2008.03.027 |pmid=22063568 |s2cid=31912208 }}

{{cite web

|url=http://www.researchgate.net/figure/Proximal-meat-composition-of-edible-cuts-of-tegu-lizard-Tupinambis-merianae-from_tbl6_51777742

|title=Table 10- uploaded by Maria Cabrera

|last1=Saadoun

|first1=A.

|last2=Cabrera

|first2=M.C.

}}

}}

Further reading

  • {{cite web |last=Renner |first=Rebecca |author-link=Rebecca Renner |title=This dog-size lizard is spreading through the southeastern U.S. |website=National Geographic |date=2020-11-18 |url=http://www.nationalgeographic.com/animals/2020/11/tegu-lizards-invasive-spreading-southeast-united-states/ |archive-url=https://web.archive.org/web/20201118211042/https://www.nationalgeographic.com/animals/2020/11/tegu-lizards-invasive-spreading-southeast-united-states/ |url-status=dead |archive-date=November 18, 2020 |access-date=2020-11-19}}

{{Taxonbar|from1=Q24354290|from2=Q2254602}}

Category:Salvator (lizard)

Category:Reptiles described in 1839

Category:Reptiles of Argentina

Category:Reptiles of Bolivia

Category:Lizards of Brazil

Category:Reptiles of Paraguay

Category:Taxa named by André Marie Constant Duméril

Category:Taxa named by Gabriel Bibron

Category:Reptiles as pets