Erythrolamprus zweifeli ( Roze 1959 )

Ascenso, Alexandre C., Costa, João C. L. & Prudente, Ana L. C., 2019, Taxonomic revision of the Erythrolamprus reginae species group, with description of a new species from Guiana Shield (Serpentes: Xenodontinae), Zootaxa 4586 (1), pp. 65-97 : 74-76

publication ID

https://doi.org/ 10.11646/zootaxa.4586.1.3

publication LSID

lsid:zoobank.org:pub:7BBCFF79-DE38-4A79-8905-7840A1C1955F

persistent identifier

https://treatment.plazi.org/id/03DC1517-FF8A-FF8D-C7FD-2A4EFAAEFB65

treatment provided by

Plazi

scientific name

Erythrolamprus zweifeli ( Roze 1959 )
status

 

Erythrolamprus zweifeli ( Roze 1959)

Figures 3D View FIGURE 3 , 4B View FIGURE 4 , 5A View FIGURE 5 , 6D View FIGURE 6

Leimadophis zweifeli Roze 1959 ; Amer. Mus View in CoL . Novitates:4. Terra typica: Rancho Grande , Aragua, Venezuela. Holotype: MBUCV 95.

Liophis reginae zweifeli — Dixon, 1983a; Ann. Carnegie. Mus View in CoL . 52:3.

Erythrolamprus reginae zweifeli — Grazziotin et al. 2012; Cladistics. 1:21.

Liophis zweifeli — Rivas et al. 2012; Zootaxa:46.

Liophis zweifeli — Wallach et al. 2014; Snakes of the World:395.

Holotype: Adult female, MBUCV 95 View Materials , collected by J. Racenis in Setember 0 6, 1949, at the municipality of Rancho Grande, state of Aragua, Venezuela ( Fig. 4B View FIGURE 4 ).

Paratypes: Fourteen specimens, all from Venezuela : AMNH 59430 View Materials , Curupao Hydroelectric Power Plant, state of Miranda ; CM 7355 , El Limon, Caracas DF ; CM 2278 , Los Canales , Parque Nacional Natural Naiguatá, state of Miranda ; MBUCV 96 View Materials , MBUCV 621 View Materials , MBUCV 659 View Materials , MBUCV 3076–81 View Materials , Rancho Grande Biological Reservation, state of Aragua ; MBUCV 505 View Materials , Caracas Botanical Garden, Caracas DF ; MBUCV 3082 View Materials , El Estanque, Borburata, state of Carabobo ; and MBUCV 3083 View Materials , El Junquito, Cararacas DF .

Diagnosis. Erythrolamprus zweifeli is distinguished from all congeners by unique combination of the following characters: (1) dorsal scale rows 17, reducing to 15 rows after midbody; (2) apical pit single (3) ventrals 138–149 in females and 135–149 in males; (4) subcaudals 73–95 in females and 73–96 in males; (5) dorsum of head black with cream marks on proximal region of the shields; dorsal scales yellowish-cream with apical half black; (6) upper edges of supralabials black, like the head; (7) belly creamish-white with black spots; (8) lateral black spots and lateral-posterior stripe absent or indistinct; (9) ventral surface of tail creamish-white with points or spots near cloacal shield; (10) intrasulcal region of hemipenial body homogeneously ornamented with spines; (11) medial region of asulcate face of hemipenial body ornamented with slightly elongated spines organized in one to three rows, extending to the level of lobe separation; (12) sulcus spermaticus bifurcates at proximal region of hemipenial body; and (13) moderate body size (SVL 129–553 mm).

Comparisons. Erythrolamprus zweifeli shares usually cream belly with black spots of square or rhomboid shape with E. reginae , E. macrosomus , E. dorsocorallinus , and eventually E. oligolepi s regarding ventral marks. Erythrolamprus zweifeli differs from E. oligolepis by having 17 dorsal scale rows at midbody and ventral rectangular dark spots (vs. 15 dorsal scales rows at midbody and belly usually without marks); from E. reginae and E. macrosomus by having dorsal scales yellowish-cream with apical half black (vs. dorsal ground color regularly dark brown); from E. dorsocorallinus by absence of lateral-posterior stripe and dorsal scales yellowish-cream (vs. presence of lateral-posterior stripe and dorsal scales reddish or bluish-cream). Additionally, E. zweifeli differs from all subspecies of E. epinephelus by having dorsal scales yellowish-cream with apical half black (vs. dorsum of the head cream or olive green, with bands on anterior portion of body, a black spot, and a thick postorbital stripe on each side of head). Regarding the sympatric taxa, E. zweifeli differs from E. cobella , E. taeniogaster and E. breviceps by having a cream belly with rectangular marks occupying an area lower than a ventral scale (vs. cream belly scattered of complete black bands, usually occupying two ventral scales); from E. typhlus and E. poecilogyrus by having 17 dorsal scale rows in the midbody (vs. 19 dorsal scale rows in the midbody); from E. taeniurus by having 135–149 ventral scales (vs. 152–181 ventral scales); from E. miliaris by having dorsum of head black with yellow spots and 59–91 subcaudal scales (vs. dorsum of head regularly yellow and 51–64 subcaudal scales).

Redescription of the holotype. Body cylindrical; SVL 447 mm, CL 190 mm (42.5% SVL); head length 22.8 mm, height 7.8 mm, and width 11.6 mm; diameter of ocular orbit 4.3 mm; distance between orbit and rostral shield 5.7 mm; rostral triangular, 4.5 mm wide and 3.2 mm high, visible in dorsal view; internasals two, 1.9 mm length, and 2.1 mm wide; prefrontals two, 3.0 mm length, and 3.1 mm wide, in contact with supraoculars, preocular, loreal, and postnasal; frontal pentagonal, 5.9 mm length, and 4.2 mm wide; parietals two, 6.3 mm length and 4.2 mm wide; supralabials eight, second and third contacting loreal, fourth to fifth contacting eye, and sixth and seventh higher than remaining supralabials; supraoculars longer than wide; nasal divided above nostril and contacting first two supralabials, internasals, prefrontals, loreal, and rostral; loreal tetragonal, 1.3 mm length and 1.9 mm high, contacting second and third supralabials, postnasal, prefrontals, and preocular; preocular contacting supraocular, prefrontal, nasal, third and fourth supralabials; postoculars two, upper postocular higher than lower. Temporals 1+3/1+2, anterior longer than upper posterior temporal; symphysial triangular; infralabials 10, first pair in broad contact behind symphysial; first five pairs contacting chinshields; anterior chinshields 5.9 mm long; posterior chinshields 5.7 mm long; smooth dorsal scale rows 17/17/15, reduction at the level of 80 th /81 st ventrals (right/left); apical pit absent; ventrals 144; subcaudals 81; cloacal plate divided.

Dorsum of head, body and tail yellowish-cream with distal half of scales black; cream marks in anterior portion of cephalic shields; cream parietal mark starting at the level of eighth supralabial, extending into the region of contact between anterior and posterior temporal and anterolateral region of parietal scale; ventral region of body cream, with rectangular spots; tail cream, with spots or dots more concentrated on first subcaudals.

Morphometric and meristic variation (n= 98). SVL 129–553 mm (mean= 358.6; SD= 101.7; n= 97) and CL 46–221 mm (mean= 136; SD= 47; n= 97); head length 10.3–26.0 mm (mean= 18.2; SD= 3.6; n= 93), height 3.7– 9.9 mm (mean= 6.8; SD= 1.4; n= 91), and width 1.8–16.4 mm (mean= 9.8; SD= 2.4; n= 91); diameter of ocular orbit 1.0– 4.7 mm (mean= 3.4; SD= 0.6; n= 90); distance between orbit and rostral shield 2.5–6.3 mm (mean= 4.5; SD= 0.9; n= 90); rostral triangular, 2.0– 5.5 mm wide (mean= 3.6; SD= 0.8; n= 91), 1.4–6.0 mm high (mean= 2.5; SD= 0.6; n= 91); internasals 0.7–7.2 mm long (mean= 1.9; SD= 0.7; n= 92), 1.0– 3.2 mm wide (mean= 2.1; SD= 0.4; n= 91); prefrontals 1.3–3.6 mm long (mean mean= 2.4; SD= 0.5; n= 93), 1.5–3.7 mm wide (mean= 2.6; SD= 0.5; n= 93); frontal pentagonal, 3.0– 6.6 mm long (mean= 5.1; SD= 0.8; n= 93), 2.0– 4.3 mm wide (mean= 3.2; SD= 0.6; n= 93); parietals two, 2.4–8.3 mm long (mean= 6.1; SD= 1.1; n= 93), 2.2–5.5 mm wide (mean= 3.6; SD= 0.6; n= 93); loreal tetragonal, 0.5–2.3 mm long (mean= 1.3; SD= 0.3; n= 93), 0.6–2.4 mm high (mean= 1.6; SD= 0.3; n= 93); infralabials 8–10 (mean= 9.9; SD= 0.3; n= 94); infralabials contacting chinshileds 4–6 (mean= 5.0; SD= 0.2; n= 95); anterior chinshields 2.8–7.3 mm long (mean= 4.6; SD= 0.9; n= 92), posterior chinshields 2.5–6.8 mm long (mean= 4.8; SD= 1.1; n= 92); dorsal scale rows 17 with reduction at the level of 66–90/67–90 ventrals (right/ left, n= 91); ventrals 138–149 in females (mean= 143.1; SD= 2.5; n= 317), 135–149 in males (mean= 143; SD= 3.1; n= 192); subcaudals 73–95 in females (mean= 80.3; SD= 3.7; n= 39), 73–96 in males (mean= 81.4; SD= 5.1; n= 36).

Color pattern in preservative. Dorsum of head, body, and tail creamish-white with distal half of scales black; gular region and supralabials cream; cream marks on anterior region of cephalic shields; cream parietal mark starting at the level of eighth supralabial, extending to the region of contact between anterior and posterior temporal, and anterior-lateral region of the parietal; ventral surface of body creamish-white with rectangular spots; tail creamish-white with spots and points usually more concentrated on the first subcaudals ( Fig. 5A View FIGURE 5 ).

Ontogenetic variation of color in preservative. Hatchlings and juveniles with creamish-white nuchar collar (two to three dorsal scales long), a cream dorsum with the half of scales black, belly scattered with black, and the ventral surface of the tail without spots or dots.

Color in life. Dorsum of head dark grey, with yellowish-cream marks on the anterior region of cephalic shields; gular region and supralabials yellowish-cream; dorsum of head, body and tail yellowish-cream with distal half of the scales black; first two dorsal scale rows with the same pattern as the rest of the body; ventral surface of body and tail yellowish-cream with black spots ( Fig. 6D View FIGURE 6 ).

Hemipenial morphology (everted organ n= 2). Fully everted and maximally expanded hemipenes renders slightly bilobed, non-capitate, and non-calyculated organs; hemipenis with smooth apical disk on the end of lobes; hemipenial body covered by spinules, more concentrated on the marginal region of sulcus spermaticus; lobes with spinules on lateral region of asulcate and sulcate faces; sulcus spermaticus bifurcates at basal region of hemipenial body, branches with centrifugal orientation extending to central region of apical disks; basal region of sulcus with an inflated portion ornamented by elongated spines; intrasulcal region with elongate spines in a row extending into the proximal third of the sulculs spermaticus branches; proximal region of hemipenial body of asulcate face with bulges on both sides, ornamented by elongated spines; medial region of hemipenial body at asulcate face ornamented with a row of elongated spines; region around intrasulcal spines with an area without ornamentation ( Fig. 3D View FIGURE 3 ).

Geographic distribution. Erythrolamprus zweifeli occurs in mountainous regions of the Cordillera de La Costa and Cordillera de Mérida in Venezuela, as well as on the insular region of Trinidad Island ( Fig. 8 View FIGURE 8 ).

Kingdom

Animalia

Phylum

Chordata

Class

Reptilia

Order

Squamata

Family

Colubridae

Genus

Erythrolamprus

Loc

Erythrolamprus zweifeli ( Roze 1959 )

Ascenso, Alexandre C., Costa, João C. L. & Prudente, Ana L. C. 2019
2019
Loc

Liophis reginae zweifeli

Kornacker 1997
1997
Loc

Leimadophis zweifeli

Roze 1959
1959
Loc

Mus

Linnaeus 1758
1758
Loc

Mus

Linnaeus 1758
1758
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