Another new Cyrtodactylus (Squamata: Gekkonidae) from Phong Nha - Ke Bang National Park, central Truong Son, Vietnam Author Heidrich, Astrid Author Rösler, Herbert Author Thanh, Vu Ngoc Author Böhme, Wolfgang Author Ziegler, Thomas text Zootaxa 2007 1445 35 48 journal article 10.5281/zenodo.176112 9a009489-2854-46c2-943e-a8d16129db58 1175-5326 176112 Cyrtodactylus cryptus sp. n. Figures 1–6 Holotype . An adult male ( ZFMK 86037), Phong Nha - Ke Bang National Park, Quang Binh province, central Vietnam , collected by Dang Ngoc Kien on 7 July 2006 in the limestone forest of U Bo at an altitude of ca. 520 m . Description of holotype . SVL 92.5 mm; TaL 69.5 mm (of which 28.0 mm are regenerated); HL 22.0 mm; HW 17.7 mm; HH 8.8 mm; SE 9.7 mm; EE 7.4 mm; DE 3.6 mm; DEA 0.9 mm. Proportion of SVL / HL 4.21; HL / HW 1.5; HL / HH 2.5; SE / EE 1.31; DE / DEA 4.0. Rostral scale 1.4 times wider than high, paritially divided dorsally with a straight median suture extending to the centre of the scales; 10/8 supralabials, 8/8 sublabials; nares in contact with rostral, first supralabial and 3/4 nasals; nasorostrals (see Rösler 1995 , 20 p. ) between 2.5 times larger than supranasals; one internasal, half as large as nasorostrals; snout scales medially granular, flattened in the preorbital region, smooth, cycloid, juxtaposed, contacting with supralabials 2–3 times larger than median snout scales; upper ciliaries anteriorly 2–3 times larger than posterior ciliaries; head scales granular, half as large as median snout scales; head centre and temporal region with tubercles; head tubercles rounded, flat, twice the size of the surrounding granules; mental in part destroyed (presumably triangular), as large as rostral scale; two postmentals, trapezoidal, longer than wide, each contacts seven gular scales; gular scales granular, the granule being as large as median snout scales; dorsals granular, as large as median snout scales; dorsal tubercles round, conical, three times as large as dorsals, surrounded approximately by ten dorsal scales, and arranged in 20 irregular longitudinal rows; ventrals flat, smooth, those medially twice the size of dorsal scales, in 48 longitudinal rows at midbody; upper and lower arm dorsally granular, lower arm with rounded, flat tubercles that are 1.5–2 times larger than surrounding scales; upper and lower leg dorsally granular with scattered round, conical tubercles, three times as large as surrounding scales; femoral region medially sharply subdivided into large anterior and small posterior scales (see Fig. 2 ); uninterrupted series of enlarged subdigital lamellae below first finger 10/10, below fourth finger 17/18, below first toe 11/11, and below fourth toe 21/20; second, third and fourth digits with narrow skin seams; claws surrounded by a small dorsal and a large ventral scale; nine precloacal pores in a rightangled row, 26 enlarged precloacal scales; 3/3 nearly equal-sized postanal tubercles, arranged in an oblique row; original tail with whorls; dorsal tail scales flat, smooth, subimbricate, twice the size of median snout scales, arranged in regular transverse rows; the third tail whorl with nine scale rows; no enlarged subcaudal plates; subcaudals flat, smooth, imbricate, 2–3 times larger than dorsal tail scales, four rows per whorl, each of the last two per whorl enlarged; tail tubercles round, flat, 2–2.5 times the size of the surrounding scales, the first whorl with six and the fifth whorl with four tubercles; regenerated tail dorsally and ventrally with flat, smooth, imbricate scales. The dorsum of the ethanol-preserved holotype is brownish-olive; labials brown with white blotches; head above with rounded, arched and ornate brown blotches dorsally; nuchal band triangular, dark violet brown, with white margins and with a wide stripe extending from the outermost neck band corner to the posterior margin of each eye (this band is often referred to as the nuchal loop); dorsum with four dark violet-brown, narrow buff margined transverse undulate bands; the anterior dorsal band located behind the axilla, the posterior dorsal band located in the sacral region; small to larger dark violet-brown irregular blotches with narrow buff margins between the dorsal bands; flanks greyish-brown with buff blotches; venter greyish-brown; jaws and throat with white stripes and blotches; precloacal region dirty white; limbs, including fingers and toes, with white and brown stripes; original tail with white and dark brown rings; regenerated tail brown, with white blotches on the ventral side and scarcely visible white blotches on the dorsum. For the coloration and pattern in life see Fig. 1 . FIGURE 1. Male holotype of Cyrtodactylus cryptus sp. n. (ZFMK 86037) in life. Paratypes . VNUH 7.7.0 6 (adult male) and ZFMK 86038 (adult female), Phong Nha - Ke Bang National Park, Quang Binh province, central-Vietnam, collected by Dang Ngoc Kien on 7 July 2006 in the limestone forest of U Bo at an altitude of ca. 520 m . VNUH 17.7.0 6 and ZFMK 86039 (adult females), Phong Nha - Ke Bang National Park, Quang Binh province, Central Vietnam , collected in the limestone forest of Cha Noi ( 35 km from the type locality) at an altitude of 300 to 400 m : VNUH 17.7.0 6 collected by Astrid Heidrich on 5 August 2006 , and ZFMK 86039 by Ralf Hendrix on 7 August 2006 . Variation of paratypes . The single male paratype differs from the pattern of the male holotype in having only three dark transverse body bands. Its venter is whitish-grey and the tail bears ten dark and ten light alternating bands. The female paratypes have 4–5 dark transverse body bands with yellow margins, greyish-brown to whitish-grey venters and 10–11 dark brown bands on the tail. The measurements and pholidosis of the paratype series are presented in Table 1 . In addition, the female ZFMK 86038 had the postmentals in contact each with eight scales, and the dorsal tubercles surrounded by 9–11 dorsal scales. FIGURE 2. Cloacal region of the male holotype of Cyrtodactylus cryptus sp. n. (ZFMK 86037) in life. Diagnosis. A medium-sized Cyrtodactylus with a slender habitus and a maximum total length of 176.6 mm (SVL 62.5–90.8 mm) that can be distinguished from all congeners on the basis of the following combination of characters: 1) rounded body in cross-section, not wider than head; 2) neck band, extending to posterior margin of eyes; 3) dorsum with 3–5 dark transverse bands with yellow margins and dark spots; 4) ventrolateral skin folds along the body or enlarged lateral tubercles absent; 5) tubercles present on top of head, body, forearm, hind limbs and tail; 6) 19–20 irregular longitudinal rows of dorsal tubercles; 7) 47–50 longitudinal rows of ventral scales at midbody; 8) segmented tail with whorls, not depressed, base not enlarged; 9) 0–3 cloacal spurs on each side of tail base; 10) 9–11 precloacal pores in angular series in males and 16–27 enlarged precloacal scales in both sexes; 11) enlarged femoral scales and femoral pores absent; 12) precloacal groove absent; 13) subcaudals small, not transversally enlarged; 14) uninterrupted series of 20–23 lamellae beneath 4th toe; 15) tail and limbs banded. TABLE 1. Pholidosis and measurements (in mm) of the paratype series of Cyrtodactylus cryptus sp. n. (for abbreviations see material and methods); * with regenerated tail tip.

SPL	VNUH 7.7.0 6 male 11/11	VNUH 17.7.0 6 ZFMK 86038 female female 8/10 10/10	ZFMK 86039 female 10/10	min–max (χ ± s) 8–11 (9.9 ± 0.8)
SBL	6/8	9/10 8/8	9/10	6–10 (9.2 ± 1.3)
DT V	20 47	17 19 49 50	20 49	17–20 (19 ± 1.4) 47–50 (48. 8 ± 1.2)
PP	10	0 0	0	0–10 (2.5 ± 5.0)
PAT EPS	3/3 17	3/3 3/3 20 16	0/2 27	0–3 (2.5 ± 1.1) 16–27 (20 ± 4.9)
LD1	10/10	9/9 10/10	10/10	9–10 (9.8 ± 0.5)
LD4 LT1	19/19 12/11	18/19 19/18 9/9 10/10	19/19 11/11	18–19 (18.8 ± 0.5) 9–12 (10.4 ± 1.1)
LT4	23/23	21/20 22/21	23/20	20–23 (21.6 ± 1.3)
SVL TaL	74.04 75.82	84.04 86.61 63.59* 87.05	84.84 88.42	74.04–84.84 (82.4±5.66) 63.59–88.42 (78.7±11.6)
SE EE	8.37 6.94	9.37 9.84 7.51 8.04	9.52 7.52	8.37–9.84(9.3±0.6) 6.94–8.04(7.5±0.4)
HW	13.81	1.88 15.58	15.09	13.81–15.88 (15.0±0.9)
HH HL	8.69 19.63	9.29 8.87 22.37 22.77	9.77 21.64	8.69–9.77 (9.2±0.5) 19.63–22.77(21.6±1.4)
DEA	1.05	0.89 0.75	1.10	0.75–1.10 (0.9±0.2)
DE	4.50	5.27 4.79	4.44	4.44–5.27 (4.8±0.4)

FIGURE 3. One of the female paratypes of Cyrtodactylus cryptus sp. n. (ZFMK 86038) in life. Comparisons. Cyrtodactylus cryptus sp. n. can be distinguished from its Vietnamese congeners as follows (according to Taylor 1962 , 1963 , Smith 1973 , Ziegler et al. 2002 , Ngo & Grismer 2006, Youmans & Grismer 2006 , Vu et al. in press): a higher number of precloacal pores (9–11 versus 4–7) and the absence of enlarged femoral scales distinguish it from C. condorensis (Smith, 1920) ; the absence of enlarged subcaudal plates, enlarged femoral scales and femoral pores distinguish it from C. intermedius (Smith, 1917) , C. phongnhakebangensis Ziegler et al. 2002 and C. variegatus (Blyth, 1859) ; a higher number of precloacal pores (9– 11 versus 5–7 and 4, respectively) and the absence of femoral pores and enlarged femoral scales distinguish it from C. irregularis (Smith, 1921) and C. quadrivirgatus Taylor, 1962 ; the presence of preanal pores and a higher number of ventrals (47–50 versus 30–34) distinguish it from C. paradoxus Darevsky & Szczerbak, 1997 . FIGURE 4. One of the further records of Cyrtodactylus cryptus sp. n. in life, that shows the somewhat variable dorsal pattern; this male (Nr. 8 in Tables 2–3) was captured 31 July 0 6 at U Bo. Cyrtodactylus cryptus sp. n. may be distinguished from all other congeners from China , Laos , Cambodia , Myanmar , Thailand , Malaysia , Indonesia and the Philippines (according to Wermuth 1965 ) on the basis of the following characters: in the absence of transversely enlarged subcaudal plates it differs from C . aequalis Bauer, 2003 , C. annandalei Bauer, 2003 , C. aurensis Grismer, 2005 , C. baluensis (Mocquard, 1890) , C. chanhomeae Bauer et al., 2003 , C. consobrinus (Peters, 1871) , C. feae (Boulenger, 1893) , C. ingeri Hikida, 1990 , C. jarujini Ulber, 1993 , C. malayanus (de Roij, 1915 ), C. oldhami (Theobald, 1876) , C. peguensis (Boulenger, 1893) , C. russelli Bauer, 2003 and C. sumonthai Bauer et al., 2002 (according to de Rooij 1915 , Smith 1973 , Sharma 2002 , Grismer 2005, Grismer & Tzi Ming Leong 2005, Youmans & Grismer 2006 ). In lacking a precloacal groove the new species differs from C. cavernicolus Inger & King, 1961 , C. fumosus (Müller, 1895) , C. gansi Bauer, 2003 , C. marmoratus (Kuhl, 1831) , C. philippinicus (Steindachner, 1867) , C. pubisulcus Inger, 1957 , C. pulchellus (Grey, 1827) , C. semenanjungensis Grismer & Tzi Ming Leong, 2005 , and C. tiomanensis (Amaral 1935) (according to de Roij 1915 , Taylor 1963 , Grismer & Tzi Ming Leong 2005, Youmans & Grismer 2006 ). In the absence of femoral pores and / or enlarged femoral scales C. cryptus sp. n. differs from C. agusanensis (Taylor, 1915) , C. angularis (Smith, 1921) , C. brevipalmatus (Smith, 1923) , C. darmandvillei (Weber, 1890) , C. interdigitalis Stuart, 1999 , C. papilionoides Ulber & Grossmann, 1991 , C. redimiculus King, 1962 , C. seribuatensis Youmans & Grismer, 2006 , C. slowinskii Bauer, 2002 , C. tigroides Bauer et al., 2003 and C. wetariensis (Dunn, 1927) (after de Rooij 1915 , King 1962 , Sharma 2002 , Smith 1973 , Taylor 1963 , Ulber 1993 , Ulber & Grossmann 1991 , Batuwita & Bahir 2005 , David et al. 2004 , Youmans & Grismer 2006 ). In number of precloacal pores and / or preanal scales it differs from C. annulatus (Taylor, 1915) , C. ayeyarwadyensis Bauer, 2003 , C. chrysopylos Bauer, 2003 , C. jellesmae (Boulenger 1897) , C. laevigatus Darevsky, 1964 , C. matsuii Hikida, 1990 , C. thirakhupti Pauwels et al., 2004 , and C. yoshii Hikida, 1990 (de Rooij 1915 , Hikida 1990 , Batuwita & Bahir 2005 , Youmans & Grismer 2006 ): C. annulatus has 4–6 precloacal pores versus 9–11 in Cyrtodactylus cryptus sp. n. ; C. ayeyarwadyensis has a higher number of precloacal pores (16–29); C. chrysopylos , C. matsuii and C. yoshii have no enlarged precloacal scales versus 16–27 in the new species; C. jellesmae , C. laevigatus and C. thirakhupti have no precloacal pores versus 9–11 in the new species. The new species differs from C. buchardi David et al., 2004 in the neckband reaching the posterior margin of the eyes, the higher lamellar count under 4th toe (20–23 versus 12), and the lower number of dorsal tubercles (19–20 versus 25) ( David et al. 2004 ); it differs from C. brevidactylus Bauer, 2002 in having a higher number of subdigital lamellae below 4th toe (20–23 versus 11) and by the presence of bands and stripes on body ( Youmans & Grismer 2006 ); it differs from C. elok Dring, 1979 in having a higher number of subdigital lamellae under 4th toe (20–23 versus 18–19), in a higher number of precloacal pores (9– 11 versus 8), a higher number of ventrals (47–50 versus 44) and by the presence of bands on body ( Dring 1979 , Youmans & Grismer 2006 ); it differs from C. lateralis (Werner, 1896) in a lower number of ventrals (47–50 versus 60–64), by the absence of lateral folds and the presence of body bands (de Rooij 1915 ); and it differs from C. wakeorum Bauer, 2003 in having a higher ventral count (47–50 versus 31), a higher subdigital lamellar count under the 4th toe (20–23 versus 10) and the presence of tubercles on forelimbs ( Youmans & Grismer 2006 ). FIGURE 5. Portrait of one of the further records of Cyrtodactylus cryptus sp. n. in life; this male (Nr. 4 in Tables 2 – 3) was captured 9 July 0 6 at U Bo. C. cryptus sp. n. is further distinguishable from all other congeners from India , Sri Lanka , as well as from Australia , New Guinea and the Solomon Islands (according to Wermuth 1965 ) on the basis of the following characters: the absence of enlarged subcaudal scales from C. aaroni Günther & Rösler, 2002 , C. consobrinoides (Annandale, 1905) , C. fraenatus (Günter, 1864) , C. khasiensis (Jerdon, 1870) , C. louisiadensis (de Vis, 1892), C. murua Kraus & Allison, 2006 and C. ramboda Batuwita & Bahir, 2005 (de Rooij 1915 , Sharma 2002 , Batuwita & Bahir 2005 , Kraus & Allison 2006 ); the absence of femoral pores and enlarged femoral scales from C. biordinis Brown & McCoy, 1980 , C. deveti (Brongersma, 1948) , C. gubernatoris (Annandale, 1913) , C. loriae (Boulenger, 1898) , C. malcomsmithi (Constable, 1949) , C. mimikanus (Boulenger, 1914) , C. novaeguineae (Schlegel, 1837) , C. sadleiri Wells & Wellington, 1985 , C. soba Batuwita & Bahir, 2005 , C. subsolanus Batuwita & Bahir, 2005 and C. sworderi (Smith, 1925) ( Batuwita & Bahir 2005 , de Rooij 1915 , Sharma 2002 , Youmans & Grismer 2006 ); the presence or a higher number of precloacal pores from C. cracens Batuwita & Bahir, 2005 , that has 5–6 versus 9–11 precloacal pores in the new species, from C. edwardtaylori Batuwita & Bahir, 2005 , that has 6 versus 9–11 precloacal pores in the new species, and from C. sermowaiensis (de Rooij, 1915 ) that has no precloacal pores ( Batuwita & Bahir 2005 ); the absence of a precloacal groove from C. papuensis (Brongersma, 1934) and C . rubidus (Blyth, 1861) ( Batuwita & Bahir 2005 ) ; by a higher number of dorsal tubercle rows from C. adleri Das, 1997 , that has 11 versus 19–20 in the new species ( Das 1997 ); by a distinct pattern from C. derongo Brown & Parker, 1973 , that has a dark reddish brown dorsum with 9–10 very faint series of darker blotches each enclosing two to several large white tubercles ( Brown & Parker 1973 ). Further records. During field research within Phong Nha - Ke Bang National Park from July to August 2006, 14 additional specimens of C. cryptus sp. n. were collected by Dang Ngoc Kien, Astrid Heidrich, Ralf Hendrix and local people. They were identified, sexed, weighed and measured before their subsequent release (see Table 2 ). The male specimens that were captured on 6 and 10 August 2006 had 11 precloacal pores. Some sexual dimorphism in the coloration of the ventral surfaces was observed (females were somewhat darker). Coloration and pattern in two captured juveniles did not differ from that of adult specimens. In two specimens the transverse body bands were fragmented into large, broad blotches ( Fig. 4 ). TABLE 2. Mensural data (in mm) of 14 captured and released specimens of Cyrtodactylus cryptus sp. n. from Phong Nha - Ke Bang (for abbreviations see material and methods). Further abbreviations are as follows: f = female; m = male; juv. = subadult; * with regenerated tail tip; ** tail tip missing.

Nr. Date Locality	Sex	Weight [g] SVL	TaL	HL	HW
1 8 July 0 6 U Bo	juv. f	5 67.5	75.7	17.8	14.8
2 8 July 0 6 U Bo	f	7 75.6	61.4*	21.1	16.9
3 9 July 0 6 U Bo	f	7.5 82.1	78.2	21.8	15.9
4 9 July 0 6 U Bo	m	10 76.5	90.4	21.8	16.1
5 30 July 0 6 U Bo	m	8 73.0	86.2	19.4	15.4
6 30 July 0 6 U Bo	juv. m	5 62.5	50.0*	16.5	12.9
7 31 July 0 6 U Bo	f	6 67.3	80.0	19.8	15.0
8 31 July 0 6 U Bo	m	7 66.0	49.0*	18.3	14.3
9 6 August 0 6 Cha Noi	f	6.5 74.0	39.0**	19.9	14.2
10 6 August 0 6 Cha Noi	m	8 76.3	82.3*	21.2	15.8
11 7 August 0 6 Cha Noi	f	13 90.8	62.8	24.1	23.0
12 10 August 0 6 Cha Noi	f	8 72.9	78.9	18.9	14.0
13 10 August 0 6 Cha Noi	m	6.5 71.8	77.0	19.1	14.0
14 23 August 0 6 U Bo	m	9.5 81.2	54.2*	21.2	16.0

. Etymology. The name of the species derives from the Greek adjective kryptos (Latin cryptus ) meaning “concealed”, “hidden”, because the new species had been overlooked during the previous decade of herpetological investigations in the Phong Nha - Ke Bang National Park. FIGURE 6. Male holotype of Cyrtodactylus cryptus sp. n. (ZFMK 86037) in life in its microhabitat at the type locality. Natural history and distribution. All observations of Cyrtodactylus cryptus sp. n. took place at night. Specimens were found on karst cliffs, on tree trunks and in branches or leaves up to 2 m height, but also on rotten trees, on stones and one specimen even on the ground on a forest street. For climate and microhabitat information see Table 3 . In the U Bo region, C. cryptus sp. n. was the only bent-toed gecko we were able to record and the new species inhabited both karst cliffs and tree trunks ( Figs. 6–7 ). In the second site of the Phong Nha - Ke Bang National Park, where we recorded the new species (in Cha Noi area, Fig. 8 ), C. cryptus sp. n. occurred in sympatry with C. phongnhakebangensis . According to our observations it seems that these two species inhabit different microhabitats when occurring together, with C. cryptus sp. n. mainly occupying tree trunks and C. phongnhakebangensis karst cliffs. In the U Bo area we marked eight individuals of the new species along 138 m of karst stream. After three weeks, three animals (37.5 %) were recaptured up to 5 m away from the original collecting locations. However, similar studies carried out in the primary forest gave different results: A male and a female were released on a tree trunk distant from streams and karst cliffs, and recaptured during the subsequent two nights. However, we failed to see these animals during searches conducted ten days later. During capture-recapture studies we only were able to recapture C. cryptus sp. n. on karst cliffs, but never on primary forest trees. Detailed data concerning capture-recapture research and the feeding ecology of C. cryptus sp. n. will be published elsewhere (Heidrich et al., in prep.). One female specimen, kept in a terrarium for some time laid two hard-shelled, oval eggs of 12 x 14.3 mm size on 28 September , 2006, in the early rainy season. Both eggs were deposited in a tube-shaped stone hole. Currently, the species is known only from its type locality ( Fig. 9 ). TABLE 3. Ecological details for the 14 captured and released specimens of Cyrtodactylus cryptus sp. n. from Phong Nha - Ke Bang. Abbreviations are as follows: f = female; m = male; juv. = subadult; Temp. = temperature.

Nr.	Date	Locality	Sex	Time	Temp.	Humidity	Microhabitat
1	8 July 0 6	U Bo	juv. f	20:50	25°C	90%	karst cliff, in 1.7 m height
2	8 July 0 6	U Bo	f	22:16	26°C	90%	karst cliff, in 1 m height
3	9 July 0 6	U Bo	f	22:50	24°C	93%	karst cliff, in 2 m height
4	9 July 0 6	U Bo	m	23:22	24°C	93%	karst cliff, in 0.3 m height
5	30 July 0 6	U Bo	m	20:30	23°C	88%	tree trunk, in 1.3 m height
6	30 July 0 6	U Bo	juv. m	21:10	25°C	80%	karst cliff, in 0.3 m height
7	31 July 0 6	U Bo	f	00:13	24°C	87%	tree, in 0.5 m height
8	31 July 0 6	U Bo	m	00:42	23°C	92%	ground, (forest street)
9	6 August 0 6	Cha Noi	f	20:15	25°C	93%	branch, in 0.5 m height
10	6 August 0 6	Cha Noi	m	20:30	25°C	93%	rotten tree, in 0.5 m height
11	7 August 0 6	Cha Noi	f	22:20	25°C	95%	stone, in 1.0 m height
12	10 August 0 6	Cha Noi	f	22:56	26°C	84%	leaves, in 1.2 m height
13	10 August 0 6	Cha Noi	m	23:00	26°C	84%	branch, in 1.0 m heigth
14	23 August 0 6	U Bo	m	19:31	24°C	90%	branch, in 0.5 m height

FIGURE 7. In U Bo, Cyrtodactylus cryptus sp. n. was found along such forest streams. Systematic position. Among the species of Cyrtodactylus distributed in South East Asia , C. cryptus sp. n. is mainly characterised by the absence of enlarged subcaudals, a precloacal groove, femoral pores and enlarged femoral scales. The new species is superficially similar in colouration and pattern to the sympatric C. phongnhakebangensis . However, C. cryptus sp. n. is clearly set apart from C. phongnhakebangensis among others by lacking enlarged subcaudal plates, femoral pores and enlarged femoral scales, as well as by a lower number of precloacal pores. C. cryptus sp. n. is very similar to C. papilionoides in habitus, body size and colour pattern ( Ulber & Grossmann 1991 , Chan-Ard et al. 1999), but differs in the presence of round and flat tail tubercles versus pointed tail tubercles in C. papilionoides , the lack of enlarged femoral scales, a higher number of ventral scales (47–50 versus 30–34 in C. papilionoides ), the presence of a continuous series of 20– 23 subdigital lamellae under the 4th toe versus an interrupted series of 12–16 lamellae under the 4th toe and 3– 7 scales, a higher number of longitudinal rows of dorsal tubercles (19–20 irregular versus 12–14 regular) and precloacal pores (9–11 versus 4–6), which are arranged in acute-angled rows (versus obtused-angled rows in C. papilionoides ), as well as by having larger precloacal scales (compared with ventral and femoral scales). Furthermore, the two species have different egg shapes (oval in C. cryptus , almost round in C. papilionoides , with a diameter of 14.9 x 14.0 mm according to Schäfer 1991 ). Future (molecular) analyses must clarify the systematic relationships of the new species.