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Liolaemus darwinii (BELL, 1843)

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Higher TaxaLiolaemidae, Iguania, Sauria, Squamata (lizards)
Subspecies 
Common NamesE: Darwin's Tree Iguana 
SynonymProctotretus darwinii BELL 1843: 20
Liolaemus darwinii — GRAY 1845
Eulaemus darwini — GIRARD 1857
Liolaemus darwinii — BOULENGER 1885: 155
Liolaemus darwinii — MÜLLER & HELLMICH 1938
Liolaemus darwinii — CEI 1993
Liolaemus (Eulaemus) darwinii — SCHULTE et al. 2000
Liolaemus darwinii — CAMARGO et al. 2012
Liolaemus (Eulaemus) darwinii — MORANDO et al. 2020
Liolaemus darwinii — AVILA et al. 2021 
DistributionArgentina (Patagonia; from SE Catamarca and SW Santiago del Estero southward to Rio Negro, and eastward to the Atlantic coast between S Buenos Aires and Chubut provinces, Mendoza, Neuquén, La Rioja)

Type locality: Bahia Blanca, Northern Patagonia, Argentina  
ReproductionOviparous 
TypesSyntypes: BMNH xii.90.a-b (renumbered 1946.8.10.21-22). 
DiagnosisDiagnosis: “Liolaemus darwinii may be distinguished from all other species in the L. darwinii complex save L. laurenti and L. olongasta by the presence of intensely dark pigment within the antehumeral fold in adult males, and from L. laurenti and L. olongasta by the presence of conspicuously enlarged, dark brown or black prescapular and postscapular spots in adult males.” (Etheridge 1993: 148).

Variation. “Maximum adult size, and variation in tail/total length, scale counts and precloacal pore numbers are given in Tables 1-4. According to Gallardo (1966) L. darwinii and L. wiegmannii differ from other similar species in lacking an azygous frontal; however, this character is variable in both species. The lectotype is a subadult male and does not now exhibit the pattern characteristic of adult males of this species.” (Etheridge 1993: 149).

Coloration: “Adult males nearly always have dorsolateral light stripes that are conspicuous on the neck and anterior body due to bright creamy-yellow scales, continuing posteriorly on body and tailor, more often, posteriorly fragmented. The middorsal light stripe is usually present and continuous, but inconspicuous, and the ventrolateral stripes absent or represented by a broken line. Paravertebral spots are usually discrete, little changed from standard pattern; prescapular and postscapular lateral spots are enlarged and dark, usually separate, sometimes contiguous. The sides of the body are usually without additional lateral dark spots and have light spots or a broken reticulum. The prescapular spot is continuous ventrally with the very dark pigment within the antehumeral fold, which in turn is continuous ventrally with dark pigment on the sides of the anterior chest region. The dorsal ground color is tan or light brown, sometimes tinged with brick-red. Cei (1986: Lam. 18) provided color photographs of both sexes.
The pattern ofventral pigmentation is subject to ontogenetic change, and is variable among adult males within any population. Neonates of both sexes have a nearly immaculate white venter, or with some indistinct spotting on the throat. In males the throat markings become more conspicuous, and dark spots appear on the belly. The dark pigmentation within the antehumeral fold expands downward in front of the forelimbs, and thence medially toward the middle of the throat, and eventually may form a complete transverse bar across the posterior throat and anterior chest. As the throat bar is developing, a large patch ofdark pigment may appear on the anterior surface ofeach thigh, and a region ofvery dark pigment may develop on the abdomen. In 26 samples that included adult males from throughout the range of the species, in all but two samples at least some specimens exhibited a throat bar. Thigh patches occurred in at least some males of all but three samples, and dark abdominal pigmentation was present in at least some males of eight samples. In most of the samples examined, the great majority of males had at least some indication ofthe transverse chest bar and thigh patches, but there is no discernable geographic pattern to this variation; the degree ofdevelopment ofventral pigmentation appears to be independent ofactual size in adults, and the lack of males with abdominal pigment occurs mostly in samples of small size. Geographic patterns of the development of ventral pigmentation in L. dwwinii eventually may be detected, but at present the data are insufficient.
Adult females variable, with standard pattern ofstripes and spots present or variously reduced, some virtually without a dorsal pattern except for ventrolaterallight stripes. Some adult females with prescapular and postscapular spots slightly enlarged and darkened, and with grey pigment in antehumeral fold. Throat with dark spots and streaks, belly immaculate or spotted.” (Etheridge 1993: 149). 
CommentLiolaemus darwinii, together with L. ornatus, L. irregularis and L. uspallatensis, form the L. darwinii complex.

Distribution: not in Chile (fide D. Pincheira-Donoso, pers. comm., 23 May 2017).

Member of the darwinii group of Liolaemus. 
EtymologyNamed after Charles Robert Darwin (1809-1882), author of “On the Origin of Species ...”. 
References
  • Abdala, C.S. 2005. Una nueva especie del género Liolaemus perteneciente al complejo darwinii (Iguania:Liolaemidae) de la provincia de Catamarca, Argentina. Revista Española de Herpetologia 19:5-17 - get paper here
  • Abdala, C.S. 2007. Phylogeny of the boulengeri group (Iguania: Liolaemidae, Liolaemus) based on morphological and molecular characters. Zootaxa 1538: 1-84 - get paper here
  • ABDALA, CRISTIAN SIMÓN; ANDRÉS SEBASTIÁN QUINTEROS,, FEDERICO ARIAS, SABRINA PORTELLI & ANTONIO PALAVECINO 2011. A new species of the Liolaemus darwinii group (Iguania: Liolaemidae) from Salta Province, Argentina. Zootaxa 2968: 26–38 - get paper here
  • Avila, L. J. and J. C. Acosta. 1993. Notas sobre el comportamiento de Liolaemus darwini (Sauria: Tropiduridae) en el sur de la Provincia de Mendoza. Facena 10: 57-61 - get paper here
  • AVILA, LUCIANO JAVIER; LORENA ELIZABETH MARTINEZ & MARIANA MORANDO 2013. Checklist of lizards and amphisbaenians of Argentina: an update. Zootaxa 3616 (3): 201–238 - get paper here
  • Avila, Luciano Javier; Martín Miguel Femenías, Cristian Hernán Fulvio Pérez, Mariana Morando 2021. Nuevas especies de Liolaemus para la herpetofauna de la provincia de La Rioja, Argentina. Cuadernos de Herpetología 35 (S1): 223-228
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  • BRIZIO, M. V., MINOLI, I., PÉREZ, D. R., & AVILA, L. J. 2023. Reptiles of the Auca Mahuida natural protected area, Argentina. Rev. Mus. Argentino Cienc. Nat., n.s. 25(1): 133-142 - get paper here
  • Camargo, Arley; Luciano J. Avila, Mariana Morando, and Jack W. Sites, Jr 2012. Accuracy and Precision of Species Trees: Effects of Locus, Individual, and Base Pair Sampling on Inference of Species Trees in Lizards of the Liolaemus darwinii Group (Squamata, Liolaemidae). Systematic Biology 61: 272-288 - get paper here
  • Etheridge, R. 1993. Lizards of the Liolaemus darwinii complex (Squamata: Iguania: Tropiduridae) in Northern Argentina. MUSEO REGIONALE DI SCIENZE NATURALI BOLLETTINO (TURIN). 11 (1): 137-199
  • Etheridge, R. 2000. A review of lizards of the Liolaemus wiegmannii group (Squamata, Iguania, Tropiduridae), and a history of morphological change in the sand-dwelling species. Herpetological Monographs 14: 293-352 - get paper here
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  • SCHULTE II, JAMES A.; J. ROBERT MACEY, ROBERT E. ESPINOZA AND ALLAN LARSON 2000. Phylogenetic relationships in the iguanid lizard genus Liolaemus: multiple origins of viviparous reproduction and evidence for recurring Andean vicariance and dispersal. Biological Journal of the Linnean Society 69: 75–102 - get paper here
  • Scrocchi, Gustavo J.; Cristian S. Abdala,Javier Nori, Hussam Zaher 2010. Reptiles de la provincia de Río Negro, Argentina. Fondo Ed. Rionegrino, 249 pp.
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  • Tulli, M.J.; F.B. Cruz, A. Herrel, B. Vanhooydonck, V. Abdala 2009. The interplay between claw morphology and microhabitat use in neotropical iguanian lizards. Zoology 112 (5): 379-392 - get paper here
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