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Ateuchosaurus okinavensis (THOMPSON, 1912)

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Higher TaxaScincidae, (Ateuchosauridae, Ateuchosaurini), Scincoidea, Sauria, Squamata (lizards)
Subspecies 
Common NamesE: Ryukyu short-legged skink 
SynonymLygosoma okinavensis THOMPSON 1912: 4
Lygosaurus pellopleurus HALLOWELL 1861: 496–497 (part)
Lygosaurus pellopleurus — STEJNEGER 1907: 222–224 (part)
Lygosaurus pellopleurus — STEJNEGER 1927: 2
Lygosaurus pellopleurus — VAN DENBURGH 1912a: 7 (part)
Lygosaurus pellopleurus — VAN DENBURGH 1912b: 240–241 (part)
Lygosaurus pellopleurus — SCLATER 1950: 114.
Lygosoma pellopleurum — BOULENGER 1887: 319
Lygosoma pellopleurum — OKADA 1891: 70
Lygosoma (Homolepida) pellopleurus — BOETTGER 1895: 107
Ateuchosaurus pellopleurus — SMITH 1937: 231
Ateuchosaurus pellopleurus — TANAKA 1979: 37 (part)
Ateuchosaurus pellopleurus — HIKIDA 1996: 81 (part)
Ateuchosaurus pellopleurus — OTA et al. 1999: 106 (part)
Ateuchosaurus pellopleurus — GORIS & MAEDA 2004: 155–156 (part)
Ateuchosaurus pellopleurus — AUSTIN & ARNOLD 2006: fig. 2, table 1
Ateuchosaurus pellopleurus — PYRON et al. 2013: fig. 7
Ateuchosaurus pellopleurus — HEDGES 2014: 322
Ateuchosaurus pellopleurus — ZHENG & WIENS 2016: figs 1–2
Ateuchosaurus pellopleurus — OKAMOTO 2017: table 5.2
Ateuchosaurus pellopleurus — MAKINO et al. 2020: 7 (“southern lineage”)Ateuchosaurus pellopleurus — OKAMOTO & KURITA 2021: 142–143 (part)
Lygosoma pellopleurus — OKADA 1939: 206–209 (part).
Lygosoma (Ateuchosaurus) pellopleurum — NAKAMURA & UÉO 1963: 123 (part)
Ateuchosaurus okinavensis — MAKINO et al. 2023 
DistributionJapan (Ryukyu Archipelago: Okinawa Group)

Type locality: Nago, Okinawaji- ma Island, Okinawa Group, Ryukyu Archipelago, Japan  
Reproduction 
TypesHolotype: CAS 21537; other specimens: KUZ, OMNH 
DiagnosisDiagnosis: An Ateuchosaurus species characterized by the following: usually fused FrNa and frontal; a pair of frontoparietals that do not contact each other; eight SuCis; anteroposteriorly reduced parietals separated from SuO and pretemporal by EcP; no distinct nuchals; usually six InLas; body size medium (SVL ca. 42–70 mm); widely separated forelimb and hindlimb when appressed; usually 26 or 28 MSRs (mode = 28, 25– 28); 54–64 (mode = 59) and 55–67 DMSs (mode = 58) in male and female, respectively; 10–16 TIVs (mode = 13); 10 preanals not enlarged; usually no black stripe on dorsal scale row or one pair of DSRBS; a karyotype of 2n = 28 (Ota et al. 1998). (Makino et al. 2023)

Comparisons. Ateuchosaurus okinavensis, together with A. pellopleurus, is distinguished from A. chinensis by having the following characters (Nguyen et al. 2008): usually six InLas (vs. seven InLas); smaller body size (SVL ca. 42–70 mm vs. 70.0–83.8 mm; see also Okamoto and Kurita 2021); usually 26 or 28 MSRs (vs. 30 scale rows); usually 10–14 TIVs (vs. usually 16–18 TIVs); 10 preanals (vs. usually six preanals); blackish line on dorsolateral surface from snout to midbody (vs. no such line). This species also is distinguished from A. chinensis by the karyotype of 2n = 28 (vs. 2n = 26; no information about the karyotype of A. pellopleurus; Ota et al. 1998). Ateuchosaurus okinavensis resembles A. pellopleurus in MSR and body size but differs in almost having a fused FrNa and frontal (vs. separated ones), 54–64 and 55–67 DMSs in male and female (vs. 53–70 and 56–69 DMSs in male and female), 10–16 TIVs (vs. 8–14 TIVs), usually 0–1 pair of DSRBS (vs. usually 2–3 pairs). The mean K2P distance ± standard deviation (range in parenthesis) based on cytochrome b sequences between A. okinavensis and A. chinensis was 24.7% ± 0.3% (23.9%–25.5%); the value between A. okinavensis and A. pellopleurus, see Comparison of A. pellopleurus. (Makino et al. 2023)

Description. Mainly based on a specimen (KUZ R77462), an adult male collected from Ogimi Village in Okinawajima Island (26°41'44.88"N, 128°07'31.14"E, 111 m above sea level) (followed by ranges of several morphometric and meristic characters in parenthesis; N = 13 collected from Ogimi Village, KUZ R70673– 70674, 77446, 77451–77454, 77458–77462, 77464); SVL 54.4 mm (55.0 ± 4.4, 49.8–64.8); HL 6.7 mm (6.3 ± 0.4, 5.7–7.0); HW 5.4 mm (5.5 ± 0.4, 5.1–6.1); HH 3.8 mm (3.8 ± 0.3, 3.3–4.4); SEyL 3.2 mm (3.1 ± 0.2, 2.8–3.4); EyL 2.3 mm (2.3 ± 0.2, 2.0–2.6); EyEaL 3.3 mm (3.0 ± 0.3, 2.6–3.3); EaD 1.0 mm (1.1 ± 0.1, 0.9–1.4); SAL 19.3 mm (19.2 ± 1.5, 16.7–21.8); AGL 31.1 mm (31.8 ± 2.8, 27.5– 37.5); TaL 38.8 mm (the tip of tail lost; the remaining tail original; 61.4 ± 3.5, 57.6–64.5, N = 3 with undamaged original tail); FlL 8.5 mm (8.9 ± 0.9, 7.5–10.2, N = 12); HlL 14.3 mm (14.2 ± 1.0, 12.3–15.5); FIIIL 2.0 mm (1.9 ± 0.2, 1.6–2.3, N = 12); TIVL 4.4 mm (4.3 ± 0.4, 3.5–5.1). Snout obtusely pointed; rostral visible from above, overlapping supranasal and nasal; nasal fused with first supralabial, with no groove on boundary between nasal and labial parts; nostril at center of nasal part of nasal; supranasal unpaired with posterior edge concaved, overlapped by nasal; supraloreal overlapped by supranasal and anterior and posterior loreals, overlapping frontonasal part and first supraciliary; frontonasal and frontal fused, frontonasal part overlapped by supranasal, overlapping first supraocular, frontal part overlapping frontoparietals and interparietal; no prefrontal; four supraoculars (no variation, N = 12), anterior ones overlapping posterior ones, first one overlapped by first, second and third supraciliaries, first and second ones overlapping frontal part, third and fourth ones overlapping frontoparietal; a pair of frontoparietals as long as width, separated from each other by interparietal, overlapping interparietal, parietal and ectoparietal; interparietal with short arrowhead-like tetragonal shape, a little longer and narrower than frontoparietal, overlapping parietals; ectoparietal pentagonal, shorter than and as wide as fourth supraocular, overlapped by fourth supraocular and upper pretemporal, overlapping parietal; parietals shorter and almost 1.2 times wider than interparietal, separated from each other by interparietal; no distinct nuchal. Two loreals with a half length and similar height of second supralabial, anterior one overlapped by nasal, overlapping supranasal, posterior one and second supralabial, posterior one overlapped by second supralabial, overlapping first supraciliary and upper and lower preoculars; eight supraciliaries (mode = 8, 8–9), anterior ones overlapping posterior ones, first one overlapped by upper preocular, third and fourth ones overlapping second supraocular, fifth and sixth ones overlapping third supraocular, seventh one overlapping fourth supraocular, eighth one overlapping upper pretemporal and upper postocular; two preoculars, upper one similar size to first supraciliary, overlapped by lower one, lower one larger than upper one, overlapped by second supralabial, overlapping third supralabial; two presuboculars, anterior one overlapped by lower preocular in left side (overlapped by third supralabial and lower preocular in right side), overlapping third supralabial and posterior one in left side (overlapping posterior one in right side), posterior one overlapped by third supralabial, overlapping fourth supralabial; three postsuboculars, lower ones overlapping upper ones, lowermost one largest, overlapped by fourth supralabial, lowermost and middle ones overlapping fifth supralabial, middle and uppermost ones overlapping primary temporal, uppermost one overlapping anterior and lower postoculars; three postoculars, anterior one overlapping upper and lower ones, upper one overlapping lower one; two pretemporals, upper one overlapped by fourth supraocular and upper postocular, overlapping lower one and uppermost secondary temporal, lower one smaller than upper one, overlapped by upper and lower postoculars, overlapping first to third secondary temporals; temporals with similar shape and size of body scale; single primary temporal overlapped by lower postocular and fifth supralabial, overlapping sixth supralabial; four secondary temporals, uppermost one overlapped by ectoparietal, second one overlapped by uppermost one, third one overlapped by primary temporal and second one on left side (overlapped by primary temporal, overlapping second one on right side), lowermost one overlapped by primary temporal, third one and sixth supralabial, overlapping upper postlabial; six supralabials (no variation), anterior ones overlapping posterior ones, fourth and fifth ones largely interrupted by lower-anterior postsubocular, fifth one longest, third to fifth ones under eye; two postlabials overlapped by sixth supralabial, upper one overlapping lower one. Mental as wide as and lower than rostral, overlapping postmental and first infralabial; single postmental as long as and narrower than mental, overlapped by first infralabial, overlapping chinshields; six infralabials on left side (five on right side, mode = 6, 4–7), anterior ones overlapping posterior ones, first one overlapping chinshield, sixth one smallest; a pair of chinshields, separated from each other, smaller than postmental, overlapped by second infralabial, overlapping postgenial; a pair of postgenials, smaller than chinshields, overlapped by second and third infralabials. Ear opening with oval shape, no ear lobule; forelimbs with five short but distinct fingers, third one longest; third finger with supradigital scales of single row at tip and two rows at base and eight subdigital scales (mode = 7, 7–8, N = 12); 25 scale rows around midbody (mode = 26, 25–28); 59 pairs of dorsal median scales from posterior side of parietal to position of posterior margin of preanal (mode = 56, 55–61); usually three keels on a dorsal scale; hindlimbs with five distinct toes, fourth one longest; fourth toe with three rows of supradigital scales at base and 14 subdigital scales (mode = 14, 13–16); 10 preanals, central ones with shorter length and similar width of midbody scales, overlapped by outer ones, right-central one overlapped by left-central one, outermost ones small; subcaudal not enlarged; 18 scale rows around tail at 10th subcaudal position. (Makino et al. 2023)

Coloration in alcohol: dorsal surface of head to tail light brown, first scale row from dorsal median line on midbody marginally darker with small blackish spots; no distinct blackish stripe on dorsal scale row (mode = 0, 0–1); first scale row from dorsal median line on original tail with a pale blackish stripe; upper and lower eyelids whitish with blackish edge; blackish line on dorsolateral surface from snout to midbody interrupting dorsal and lateral sides, with narrower width of second supralabial on snout, interrupted by eye, with similar width of dorsolateral scale from eye to neck, 1.0–1.5 times wider than dorsolateral scale at position above forelimb, obscure from that position to midbody; upper margin of blackish line distinct from posterior corner of eye to midbody, located on middle position of scales on fourth scale row from dorsal median line; lateral surface of head to neck brownish white with many black spots; lateral surface of upper and lower jaws with several black spots; lateral surface around forelimb to tail dark brown; ventral surface pale yellow from head to tail, with many short stripes and spots irregularly scattered in head, black spots between hindlimb, and a pale black spot on each scale in tail; dorsal surface of forelimb dark brown with a rough blackish line on each scale row; ventral surface of forelimb pale yellow without blackish line; dorsal surface of hindlimb dark brown with a blackish line on each scale row; ventral surface of hindlimb pale yellow with a blackish dotted line on each scale row.)(Makino et al. 2023)

Variation. For SuNa, this species usually shows a single scale with a concave posterior edge (84/104 specimens), and sometimes two laterally separated scales (1/104 specimens) or a single scale with an almost straight posterior edge (19/104 specimens). This species usually has a long fused FrNa and frontal scale, but sometimes FrNa and frontal are distinct (Table 1; Ota et al. 1999). In the Tokashikijima population, males have smaller DMSs (mode = 57, 54–61) than females (mode = 60, 56–62). Mitochondrial DNA sequences differ among the four groups of Iheyajima and Izenajima Islands (site 14 and the adjacent island), the northern part of Okinawajima Island (site 15) and the adjacent islets (including site 16), the southern part of Okinawajima Island and the islands of the Kerama Group (site 19 and the adjacent islets), and Agunijima, Tonakijima, and Kumejima Islands (sites 20– 22) (Makino et al. 2020). The populations in the northern and southern parts of Okinawajima Island have different RAG1 allele compositions (Makino et al. 2020). (Makino et al. 2020, Makino et al. 2023). 
CommentDistribution: see map in Makino et al. 2020 (Fig 1) and Makino et al. 2023: 78 (Fig. 1).

For more references see Makino et al. 2023.

Synonymy: OKADA 1939 synonymized Lygosoma okinavensis with Lygosaurus pellopleurus; Makino et al. 2023 revalidated okinavensis. 
EtymologyNamed after the type locality. 
References
  • Barbour, T. 1917. A most regretable tangle of names. Occasional Papers of the Museum of Zoology, University of Michigan (44): 1-9 - get paper here
  • Barbour, Thomas 1909. Notes on Amphibia and Reptilia from Eastern Asia. Proc. New England zool. Club 4: 53-78, 2 plates - get paper here
  • Boettger, O. 1895. Neue Frösche und Schlangen von den Liukiu-Inseln. Offenbach. Ver. Naturk. 33-36: 101-117
  • Boulenger, G. A. 1887. Catalogue of the lizards in the British Museum (Nat. Hist.) III. Lacertidae, Gerrhosauridae, Scincidae, Anelytropsidae, Dibamidae, Chamaeleontidae. London: 575 pp. - get paper here
  • Goris, R.C. & Maeda, N. 2004. Guide to the Amphibians and Reptiles of Japan. Krieger, Malabar, 285 pp.
  • Hallowell, E. 1861. Report upon the Reptilia of the North Pacific Exploring Expedition, under command of Capt. John Rogers, U. S. N. Proc. Acad. Nat. Sci. Philadelphia 12 [1860]: 480 - 510 - get paper here
  • Makino T, Nakano T, Okamoto T, Hikida T 2023. Taxonomic revision and re-description of Ateuchosaurus pellopleurus (Hallowell, 1861) (Reptilia, Squamata, Scincidae) with resurrection of A. okinavensis (Thompson, 1912). Zoosystematics and Evolution 99(1): 77-91 - get paper here
  • Makino, T., Okamoto, T., Kurita, K., Nakano, T., & Hikida, T. 2020. Origin and intraspecific diversification of the scincid lizard Ateuchosaurus pellopleurus with implications for historical island biogeography of the Central Ryukyus of Japan. Zoologischer Anzeiger 288: 1-10 - get paper here
  • Nakamura, Yasuyuki, Akio Takahashi and Hidetoshi OTA. 2013. Recent cryptic extinction of squamate reptiles on Yoronjima Island of the Ryukyu Archipelago, Japan, inferred from garbage dump remains. Acta Herpetologica 8 (1): 19-34
  • Ota, Hidetoshi;Lin, Jun-Tsong;Bogadek, Anthony;Lau, Michael W. 1997. Karyotype of the lygosomine genus Ateuchosaurus from East Asia. Journal of Herpetology 31 (4): 604-607 - get paper here
  • Ota,H.; Miyaguni,H. & Hikida,T. 1999. Geographic variation in the endemic skink, Ateuchosaurus pellopleurus, from the Ryukyu Archipelago, Japan. Journal of Herpetology 33 (1): 106-118 - get paper here
  • Sclater, J.A. 1950. Bionomic notes on some reptiles form Okinawa Shima, Ryukyu Islands, Japan. Ann. Mag. Nat. Hist. (12) 3: 113-116 - get paper here
  • Smith, M.A. 1937. A review of the genus Lygosoma (Scincidae: Reptilia) and its allies. Records of the Indian Museum 39 (3): 213-234
  • Stejneger, LEONHARD H. 1907. Herpetology of Japan and adjacent territory. Bull. US Natl. Mus. 58: xx, 1-577 - get paper here
  • Thompson, J.C. 1912. Herpetological notices, No. 2. Prodrome of descriptions of new species of Reptilia and Batrachia from the Far East. Privately published, San Francisco.
 
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