Research Article |
Corresponding author: Justin L. Lee ( justinllee@verizon.net ) Academic editor: Günter Gollmann
© 2021 Justin L. Lee, Jian-Huan Yang, Platon Yushchenko, Nikolay A. Poyarkov Jr.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Lee JL, Yang J-H, Yushchenko P, Poyarkov Jr NA (2021) Rediscovery and distribution extension of the rare Kukri Snake, Oligodon hamptoni Boulenger, 1918 (Reptilia, Serpentes, Colubridae), with the first record of this species from China. Herpetozoa 34: 13-21. https://doi.org/10.3897/herpetozoa.34.e60875
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Oligodon hamptoni is a rare species of Kukri Snake known from only two specimens, both collected nearly a century ago in northern Myanmar. Here, we report the third record of this species based on a photograph taken in Mt. Gaoligongshan, Tengchong City, Yunnan Province, China, approximately 235 km northeast of the nearest record in Bhamo District, Kachin State, Myanmar. We also provide a detailed redescription of the holotype, showing that the photo record from Mt. Gaoligongshan can be unambiguously identified to this species. This rediscovery represents the first observation of O. hamptoni in China and is the first report of this species in almost 100 years.
biodiversity, Gaoligongshan Nature Reserve, morphology, Myanmar, snakes, Squamata
Kukri Snakes of the genus Oligodon (H. Boie in Fitzinger, 1826) are a speciose group of colubrid snakes widely distributed across the Asian continent as far west as Turkmenistan and as far east as the Maluku Islands of Indonesia (
Oligodon hamptoni Boulenger, 1918 represents one of the rarest Kukri Snake species in mainland Southeast Asia (Cambodia, southern China, Laos, Myanmar [Burma], Peninsular Malaysia, Thailand and Vietnam). It was described based on a single male specimen collected from “Mogok, Upper Burma” (Mogok, Pyin Oo Lwin District, Mandalay Region, Myanmar) approximately 112 years ago. Based on
On 8 October 2020, one of us (JHY) received a photograph of a moderately-sized colubrid snake from Mt. Gaoligongshan, Tengchong City, Yunnan Province, China (Fig.
Distribution of Oligodon hamptoni (red) and Oligodon lacroixi (blue). Star denotes the type locality. Localities: (1) Mogok, Pyin Oo Lwin District, Mandalay Region, Myanmar (type locality see
We inspected photographs of a snake referable to O. hamptoni from Yunnan Province, China and compared its external features to the holotype specimen (NHMUK 1946.1.1.71) from Mogok, Mandalay Region, Myanmar. The photographs were taken by Mr. Zhuan-Yun Hu, a forestry ranger in Tengchong section of Gaoligongshan National Nature Reserve (TC-GLGS, hereinafter), on his way back home after regular forest patrol. Owing to the incidental nature of the observation, the specimen observed was not collected. Instead, the photographed individual was compared directly to the holotype, along with the published description of a second specimen from Sinlumkaba, Kachin State, Myanmar (NHMUK 1930.5.8.529) given by
The holotype of O. hamptoni had a small ventral incision underneath the tail, which allowed us to confirm the sex of the specimen. Body measurements such as Snout-Vent Length (SVL), Tail Length (TailL) and Total Length (TotalL) were taken using a flexible ruler. All other head and scale measurements were taken using Mitutoyo Digital Calipers and estimated to the nearest 0.1 mm. The measurements taken include: head length, measured from the anterior margin of the jawbone (rictus) to the tip of the rostral scale (HeadL); head width, measured from the widest point between the head (HeadW); snout length, measured from the anterior point of the eye to the tip of the rostral scale (SnL); snout width, measured as a straight-line distance between the median of both nostrils (SnW); eye diameter, measured horizontally from both posterior and anterior margins of the eye (EyeD); interorbital distance, the straight-line distance between both eyes at the border of the supraoculars (IOD); frontal length, the maximum length of the frontal scale (FrontalL); frontal width, the maximum width of the frontal scale (FrontalW). Dorsal scales were counted anteriorly at one head length behind the head, at midbody, namely halfway between the terminus of the head and the vent, and posteriorly at one head length anterior to the cloacal plate (given as anterior–midbody–posterior in the description); ventral scales were counted according to
The holotype of O. hamptoni (NHMUK 1946.1.1.71) is an adult male from “Mogok, Upper Burma.” [= now Mogok, Pyin Oo Lwin District, Mandalay Region, Myanmar], collected between 1907–1908 by Mr. Herbert Hampton (Fig.
Measurements of the holotype are as follows: SVL 476 mm; TailL 69 mm; TotalL 545 mm; TailL/TotalL 0.127; HeadL 18.0 mm; HeadW 10.8 mm; SnL 6.2 mm; SnW 5.3 mm; EyeD 2.9 mm; FrontalL 4.8 mm, FrontalW 4.6 mm; IOD 6.8 mm; HeadL/W 0.60; SnL/HL 0.34; EyeD/SnL 0.47; EyeD/HeadL 0.16; FrontalL/W 1.04.
Body stout, slightly cylindrical; head barely distinct from neck, but narrower than width at midbody, ovoid in dorsal view; snout moderately elongate, ending bluntly; width of snout narrower than rest of head; tail short, tapering; nostrils subtriangular shaped, pointed laterally; eye round, large compared to head; pupil round; rostral visible from above; portion visible from above around half as long as width; rostral medially splitting prefrontals; posterior scale suture of rostral with prefrontals “deep-V” shaped, with the vertex of the rostral rising far onto the dorsal surface of the head in-line with the nostrils (narrow obtuse angle); internasals notably absent, fused with prefrontals; prefrontals subpentagonal shaped, 1.1 times wider than long; border between rostral and prefrontals round while border between frontal and supraoculars linear straight; prefrontals in contact with frontal, preocular, loreal and nasal; frontal subhexagonal and shield shaped, roughly equal in length and width, 2.8 times longer than prefrontal sutre; frontal in contact with supraoculars, prefrontals and parietals; anterior angle formed by suture of frontal bordering prefrontals broadly obtuse (~135°), eyes placed after the anterior edge of the frontal; posterior angle formed by the sutures producing the posterior vertex of the frontal narrowly obtuse (~106°); supraoculars subrectangular shaped, 2.3 times longer than wide, around three-quarters the length of frontal and one third its width; parietals subpentagonal, 1.5 times longer than wide, widest anteriorly; parietal sutre slightly shorter than frontal; parietals in contact with frontal, supraoculars, first postocular, both temporal scales and five total occipital scales; anterior parietal angle formed by the sutures between the parietal/frontal and the suture between the supraocular/parietal moderately obtuse (~125°) with the lateral ray of the angle pointing posterolaterally; nasal scale triangular, divided below the nostril, in contact with the first supralabial, loreal, prefrontal and rostral; 5/5 supralabials, second and third touching eye, fourth supralabial largest; 6/6 infralabials, first pair contacting medially, first four touching anterior chin shields; fourth infralabial the largest; 1/1 preocular; 1/1 loreal, pentagonal shaped, longer than wide; 2/2 postoculars, upper scale slightly larger than lower; 1+1 temporals, anterior temporal bordering third and fourth supralabials, posterior temporal bordering fourth and fifth supralabial. Mental scale triangular, wider than long; anterior chin shields longer than wide, round at anterior edge, linear at posterior edge; posterior chin shields equal in length to anterior chin shields; chin shields and first infralabials separated by the mental groove; three gular scales posterior to the chin shields, followed by a single preventral scale.
Dorsal scales 15–15–15, all smooth; 159 ventrals; 32 subcaudals; 192 total body scales, subcaudal ratio 0.17; cloacal plate divided; maxillary teeth 9/9, posterior teeth gradually becoming enlarged and blade-like. We did not re-examine the hemipenis of the specimen, owing to its fragile nature.
After approximately 112 years in preservation, top of dorsum with cream-colored vertebral stripe around 1.0–1.5 dorsal scales wide situated between two light-brown dorsal stripes of equal width and edged with dark-brown; stripes originate two scales below the parietal and end along the tail; vertebral stripe interrupted just before tail-tip by single brown ring; tail tip with creamy-white spot; dorsal ground color on flanks grayish-brown with small dark-brown vermiculations concentrated along the margins of the dorsal scales along with two rows of dorsolateral stripes 1.0 dorsal scales wide, slightly edged in beige, originating at nape then extending across body before merging as one single lateral stripe on the tail; uppermost pair of stripes dark-brown, immaculate anteriorly, small beige vermiculations starting at midbody; bottommost row of stripes jet black, broken-up throughout, often patterned with small dark-brown and white irregular-shaped spots; dorsal portion of head plain brown, darker-brown or black along gular region and on labials; two oblique beige-colored postocular chevrons edged with black present on head, merging on top of frontal region to form a single lyre-shaped mark; first dorsal chevron on head originating as a narrow line at the anterior portion of the frontal, extending across the temporals, supraocular and fourth and fifth supralabials as an oblique temporal bar on each side of the head before ending at the infralabials; second chevron attached to the first as wide lines along the posterior portion of frontal, tapering posteriorly past parietals before ending at the lateral portion of the nape as narrow oblique streaks; between chevrons, a light-brown spatulate spot present, partially connected to rest of nape, interrupting second chevron from connecting; snout brownish with a crescent-shaped beige-colored band present along the anterior portion of the prefrontal and edge of rostral ending at the first and second supralabials; underside of head cream-colored with irregularly-shaped black spotting concentrated on the infralabials and gular scales; venter light-cream with large black rectangular-shaped bars across the body, stopping before the cloacal plate; underside of tail same color as rest of venter but immaculate. In the original description,
The new record of O. hamptoni was observed by Zhuan-Yun Hu, a local forestry ranger of TC-GLGS, at 1656 hrs on 8th July 2020 on rural county road near Dahaoping village, Tengchong City, Yunnan Province, China (24°59.6445'N, 98°43.79'E; WGS84, 1926 m elevation) (Fig.
The coloration in life is as follows: top of dorsum with a broad yellow-beige vertebral stripe between two dusky grayish-red stripes, equal in width and edged in black; all stripes starting at nape, continuing onto tail; flanks blue-gray, interrupted by two narrow black lateral stripes merging to form a single narrow lateral stripe at the tail, bottommost lateral-stripe broken and partially interrupted by occasional irregularly shaped white spots; dorsal scales along flanks with dark-gray margins forming a weak lateral line extending from the anterior portion of the body across the tail; head reddish-brown with yellow-beige postocular streaks edged with black, first starting as narrow line above the frontal region of the head forming crescent-shaped mark before widening below the temporal region as an oblique bar, second starting before nape as a narrow-shaped chevron then extending across neck; snout same ground color as dorsum, encircled by a beige crescent-shaped preocular streak, widest above nostrils, narrowing towards the labial region. These features agree with our redescription of the type specimen and the original description from
Morphological comparison of the holotype specimen of Oligodon hamptoni (NHMUK 1946.1.1.71) with the newly recorded specimen from Baoshan, Yunnan Province, China. (A) Lateral and (B) dorsal aspects of the holotype specimen of Oligodon hamptoni (NHMUK 1946.1.1.71) from the original description (Boulenger, 1918); (C) dorsolateral aspect of the holotype specimen of Oligodon hamptoni (NHMUK 1946.1.1.71), photograph by Justin L. Lee; and (D) dorsolateral aspect of the Tengchong specimen (not collected), photograph by Zhuan-Yun Hu.
While the resolution of the photographs and video taken prevent us from obtaining accurate scale counts, we can confidentially identify the specimen to O. hamptoni based on a combination of color pattern characteristics and body proportions. The snake’s movement, size of the head in relation to the rest of the body, short tapering tail, and overall shape (referred to by birdwatchers as “GISS”, namely the overall appearance and impression of an animal) is typical of most Oligodon and eliminates almost all other colubroid snake genera found in the region. Out of the other fourteen species of Oligodon native to China, only three species have a predominately striped pattern, those being Oligodon catenatus Blyth, 1854, Oligodon eberhardti Pellegrin, 1910 and Oligodon lacroixi Angel & Bourret, 1933. The former two species are much more elongate and slender in general appearance compared to O. hamptoni and O. lacroixi, with both species possessing a brown dorsal ground color with diamond or ‘lozenge-shaped blotches that merge along the vertebral line and form a weak series of irregular stripes. Furthermore, O. lacroixi has a dark-gray dorsum with a row of small light-orange vertebral spots that is diagnostic compared to O. hamptoni. Outside of China, the only other species of Oligodon from adjacent mainland Southeast Asia that could be confused with this species is Oligodon erythrogaster Boulenger, 1907, native to Nepal and north India. Oligodon hamptoni is remarkably similar in color pattern to the species O. erythrogaster. Indeed,
External morphometric and meristic comparisons between Oligodon hamptoni and other historically grouped species. Abbreviations for morphological characters are as follows: tail length-total length ratio given as a percent (TailLR), number of maxillary teeth (MT), internasals fused with the prefrontals (INF), number of supralabials (SL), number of supralabials in contact with the eye (SLE), number of infralabails (IL), nasal scale entire or divided (NAS), loreal scale present or absent (LOR), number of preocular scales (PrO), number of postocular scales (PtO), number of anterior temporal scales (AT), number of posterior temporal scales (PT), number of dorsal scale rows counted anteriorly, at midbody and posteriorly (DSR), number of ventrals (VEN), number of subcaudals (SC), cloacal plate single or divided (CP). Sources for data in this table include
Species | TailLR | MT | INF | SL | SLE | IL | NAS | LOR | PrO | PtO | AT | PT | DSR | VEN | SC | CP |
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hamptoni | 12.7 | 9 | Yes | 5 | 2+3 | 5 | Entire | 1 | 1 | 2 | 1 | 1 | 15–15–15 | 159–174 | 30–32 | Divided |
brevicauda | 9.6–11.0 | 7–8 | Yes | 7 | 3+4 | 7 | Divided | 0 | 2 | 2 | 1–2 | 2 | 15–15–15 | 158–173 | 25–29 | Divided |
catenatus | 12.6–13.3 | 7 | Yes | 6 | 3+4 | 6 | Entire | 0 | 1 | 1–2 | 1 | 2 | 13–13–13 | 179–212 | 31–43 | Divided |
dorsalis | 16.1–19.3 | 6–7 | No | 7 | 3+4 | 7 | Divided | 1 | 1 | 1 | 1 | 2 | 15–15–13 | 162–188 | 27–51 | Divided |
eberhardti | 15.1 | 7 | Yes | 6 | 2+3 | 6 | Entire | 1 | 1 | 1 | 1 | 2 | 13–13–13 | 165–187 | 31–40 | Divided |
erythrogaster | 16.7 | 7–8 | No | 7 | 3+4 | 7 | Entire | 1 | 1 | 2 | 1 | 2 | 17–17–15 | 163–186 | 42–59 | Divided |
lacroixi | 10.5–11.5 | 8–12 | Yes | 5 | 2+3 | 6 | Entire | 0 | 1 | 2 | 1 | 2 | 15–15–15 | 162–178 | 25–34 | Divided |
mcdougalli | 13.7 | 6 | No | 7 | 3+4 | 7 | Entire | 0 | 1 | 1 | 1 | 2 | 13–13–13 | 199 | 40 | Divided |
travancoricus | 0.11–0.15 | 7 | No | 7 | 3+4 | 8 | Divided | 0 | 1 | 2 | 1 | 2 | 17–17–15 | 145–155 | 34–37 | Divided |
venustus | 13.2 | 7–8 | Yes | 6–8 | 3+4 | 7 | Divided | 0–1 | 1 | 2 | 1 | 2 | 17–17–15 | 138–165 | 27–41 | Divided |
Morphological comparisons in hemipenial morphology and color pattern between Oligodon hamptoni and other historically grouped species. The list of references corresponds to both Tables
Species | Hemipenis shape and ornamentation | Dorsal color pattern | Ventral color pattern | Distribution | References |
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hamptoni | Unilobed, calyculate and flounced along apex with spines | Broad yellow-beige vertebral stripe between two dusky grayish-red stripes | Bright red with large rectangular-black shaped bars | N Myanmar and S Yunnan Province, China |
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brevicauda | – | Reddish-brown with brown vertebral stripes | Whitish with black quadrangular spots | S India (south of Goa) |
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catenatus | Unilobed, flounced along apex, spinose throughout | Brown with lozenge-shaped vertebral spots and longitudinal stripes | Red with black quadrangular spots | NE India, N Myanmar, S China, Laos, N Vietnam |
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dorsalis | Bilobed, flounced along apex, spinose | Bluish-gray or brown with orange vertebral stripe between brownish stripes | Uniform orange or white with black quadrangular spots | NE India, Bangladesh, Myanmar |
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eberhardti | Unilobed, flounced along apex, spinose throughout | Brown with lozenge-shaped vertebral spots | Red with black quadrangular spots or dark bars | Laos, N Vietnam, S China |
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erythrogaster | Unilobed, flounced along apex, spinose throughout | Broad light-brown vertebral stripe between two dusky grayish-red stripes | Bright red with large rectangular-black shaped bars | Nepal and N India |
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lacroixi | Unilobed, ornamentation unknown | Gray with brown vertebral stripes and orange vertebral spots | Bright red with large rectangular-black shaped bars | S China, N Vietnam |
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mcdougalli | Bilobed, flounced along apex, spinose | Dusky-black, rufous-brown vertebral stripe edged with linear black spots | Black mottled with beige | S Myanmar |
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travancoricus | Unilobed, spinose at base, flounced at apex | Gray-brown with 25–33 light-edged dark crossbars | Yellow or whitish with equal proportion black quadrangular spots | S India (Western Ghats) |
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venustus | Unilobed, spinose at base, flounced at apex | Gray-brown with 23–31 dark spots | Yellowish to whitish with black quadrangular spots in equal proportion. | S India (Western Ghats) |
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The observed Oligodon hamptoni we document in this paper represents the first record of this species from China. With the recent description of Oligodon lipipengi Jiang, Wang, Li, Ding, Ding & Che, 2020 from Tibet (Che et al. 2020), this raises the number of Oligodon species known from China to fifteen. Additionally, the record from Yunnan Province represents the first live photographs ever taken of this species, and the first observation in almost 100 years.
Since
We cannot accurately assess the conservation status of O. hamptoni based on this singular observation. We do note, however, that the location of this observation is adjacent to the TC-GLGS, a member of the UNESCO World Network of Biosphere Reserves. Given the close proximity of O. hamptoni to the reserve, we can assume that the species likely occurs within this region. If true, O. hamptoni seems to be very elusive in TC-GLGS because one of us (JHY) had spent 57 field days in the reserve to conduct herpetological surveys between 2014 and 2018, which covered 1360–3000 meters in altitudinal range and different seasons, but did not obtain any record of this species (
We thank Zhuan-Yun Hu (Gaoligongshan National Nature Reserve) for providing photos/videos and observation data on the snake from Mt. Gaoligongshan. We also thank Patrick D. Campbell (Natural History Museum, London) for permission to examine the holotype of O. hamptoni and other specimens under his care. PY and NAP thank the Russian Science Foundation (RSF grant No. 19-14-00050 to NAP) for financial support.
We thank Patrick David (Muséum National d’Histoire Naturelle, Paris) and an anonymous reviewer for their helpful comments on an earlier version of this manuscript.