Contributions to Zoology, 77 (1) – 2008
An investigation into the taxonomy of Dendrelaphis tristis (Daudin, 1803): revalidation of Dipsas schokari (Kuhl, 1820) (Serpentes, Colubridae)
Johan van Rooijen1, Gernot Vogel2
Keywords: Dendrelaphis, Dendrelaphis tristis, Dipsas schokari, taxonomy, India, Western Ghats, Sri Lanka.
The taxonomic status of the colubrid snake Dendrelaphis tristis (Daudin, 1803) was investigated on the basis of morphological data taken from 64 museum specimens. Univariate and multivariate analyses of these data reveal that Dendrelaphis tristis is composed of two species. One of these species agrees with the description of Dipsas schokari Kuhl, 1820 which is revalidated in the combination Dendrelaphis schokari (Kuhl, 1820). The syntypes of D. schokari have been lost and a type for D. tristis has never been deposited in a collection. Neotypes are designated and described for both species in order to stabilize the names. D. schokari differs from D. tristis in having a lower number of ventrals and subcaudals, a larger eye, a shorter vertebral stripe and the absence of a bright interparietal spot. D. tristis and D. schokari exhibit a partially overlapping distribution. D. tristis ranges from Sri Lanka northward through most of India to Myanmar whereas the distribution of D. schokari is restricted to Sri Lanka and South-west India (Western Ghats). Although the two species coexist on Sri Lanka and in South-west India, these species presumably do not occur syntopically as suggested by their distribution patterns and morphology.
The colubrid snakes of the genus Dendrelaphis Boulenger, 1890 are widely distributed, ranging from Pakistan in the West to the northern and eastern coast of Australia in the East and South and to southern China in the North (Ziegler and Vogel, 1999). Members of the genus Dendrelaphis are slender, diurnal species that are predominantly arboreal and feed mainly on lizards and amphibians.
Boulenger (1894), Wall (1921a), Meise and Henning (1932), Mertens (1934) and Smith (1943) have in turn revised the systematics of this genus and have in turn disagreed with one another. As such, it is not surprising that the systematics of this genus have remained ambiguous as well as incomplete, a fact that was underlined by the recent descriptions of two wide-spread as well as rather common Southeast Asian species, Dendrelaphis kopsteini Vogel and Van Rooijen, 2007 and Dendrelaphis haasi Van Rooijen and Vogel, 2008.
Dendrelaphis tristis (Daudin, 1803), as hitherto defined, inhabits Sri Lanka, India, Pakistan, Bangladesh and Myanmar (Ziegler and Vogel, 1999). Daudin described D. tristis on the basis of a plate and some additional information provided by Russell (1796). A type was not deposited in a collection as was ususal at that time. D. tristis superficially resembles D. pictus (Gmelin, 1789). Consequently, Meise and Henning (1932) doubted the validity of its specific status. This illustrates the rather crude approach to the systematics of this genus at that time. D. tristis actually differs in many aspects from D. pictus. For instance, D. tristis has a substantially more stocky build, smaller vertebral scales and a conspicuous vertebral stripe which is absent in D. pictus. The names D. tristis and D. pictus in fact refer to separate clades each composed of two or more species (this report; Van Rooijen and Vogel, 2008; Vogel and Van Rooijen, in prep).
We initially examined a dozen specimens referred to D. tristis in the context of a taxonomic revision of the genus and noticed that the distribution of the number of ventral scales was bimodal. Examination of additional specimens and further research demonstrated the two superimposed distributions correspond with other differences in morphology as well as differences in coloration. This dichotomy of forms could not be attributed to sexual dimorphism and thus corresponds with two distinct taxa. In this paper, univariate and multivariate statistical techniques are used to illustrate and confirm these findings.
Material and methods
Sixty four museum specimens were examined for this study. In this sample the two forms were represented with 26 and 38 specimens. For each examined specimen, 21 characters including aspects of colour pattern, body proportions and scalation were recorded (Table 1). Eye-diameter and distance eye-nostril were measured with a slide calliper to the nearest 0.1 mm. These measurements were made on the left and right side and were subsequently averaged. Snout-vent length and tail-length were measured by marking the length on a piece of string and subsequently measuring the position of the mark to the nearest 0.5 cm. Snout-vent length was measured to the posterior margin of the anal plate. The number of ventrals was counted following Dowling (1951). Subcaudals were counted on one side, the terminal scute was excluded. The first sublabial was defined as the scale that starts between the posterior chin shield and the infralabials and that borders the infralabials (see Peters, 1964, fig. 7). The last infralabial was defined as the last infralabial still covered completely by the last supralabial. The posterior most temporal scales were defined as the scales of which more than half of the area lies in front of an imaginary line that runs from the apex of the last supralabial to the posterolateral corner of the parietal. The length of the vertebral stripe was expressed as the number of the ventral scale opposite which the stripe ends, divided by the total number of ventral scales (% VS, Thorpe, 1975).
For multivariate analyses, morphometric variables (EYED, EYEN, TAIL) were adjusted to a common SVL of 62.5 cm to correct for potential ontogenetic variation between the samples of the two species (e.g. Thorpe 1975, 1983; How et al., 1996; Turan, 1999). The following allometric equation was applied: Xadj = X - β(SVL - SVLmean ) where Xadj is the adjusted value of the morphometric variable; X is the original value; SVL is the snout-vent length; SVLmean is the overall mean snout-vent length; β is the coefficient of the linear regression of X against SVL. Linearity of the relation between SVL and each morphometric variable was checked by visual inspection of the scatter plot. The adequacy of the procedure was assessed by testing the significance of the correlation between the adjusted variables and SVL (e.g. Turan, 1999).
Table 1. List of morphometric, meristic and coloration characters used in this study and their abbreviations.
Specimens were initially assigned to one of either species on the basis of the characters VENT, SUBC, EYED and ISPOT. The initial grouping was subsequently validated by means of TwoStep Cluster analysis (SPSS, 2001; Bacher et al., 2004) using log-likelihood as distance measure and BIC as clustering criterion. This technique automatically determines the most plausible number of clusters and assigns each specimen to one of the resulting clusters. In order to illustrate the separation of the two species, a Principal Components Analysis (PCA, e.g. Wüster et al., 2001; Cramer, 2003) was performed on the characters VENT, SUBC, TAIL and EYED and the object scores corresponding with the first two principal components were plotted. Only specimens with a complete tail were included, reducing the sample by 25 specimens. Subsequently, VENT was plotted against EYED in order to include specimens with incomplete tails.
Confirmatory analyses of the differences between the two species were carried out univariately. Meristic variables were analysed with ANOVA unless the assumptions underlying this technique were violated. Species and sex were included as factors. In cases where the assumptions were violated, the nonparametric Mann Whitney U test was used. Morphometric variables (EYED, EYEN, TAIL) were analysed with ANCOVA (e.g. Maxwell and Delaney, 1990), using species and sex as factors and SVL as covariate. Qualitative variables were analysed using a χ2 test.
For analysis of geographical variation, localities were grouped into the following operational taxonomic units (OTU’s). OTU 1: Sri Lanka; OTU 2: Western Ghats, India; OTU 3: Eastern Ghats, India; OTU 4: Northeast India + Myanmar. Analysis of geographic variation was restricted to quantitative variables that did not violate the assumptions of ANOVA or ANCOVA. The analyses were carried out as described above with OTU as additional factor.
All statistical analyses were carried out with the software SPSS (2006; SPSS for Windows. Release 14.0.2. Chicago: SPSS Inc.).
Museum abbreviations: BMNH: Natural History Museum, London, United Kindom. MHNG Muséum d’Histoire Naturelle de la ville de Genève, Geneva, Swizerland. MNHN: Muséum National d’Histoire Naturelle, Paris, France. MTKD: Museum für Tierkunde, Dresden, Germany. NMW: Naturhistorisches Museum Wien, Austria. RMNH: National Museum of Natural History, Leiden, The Netherlands. SMF: Natur-Museum und Forschungs-Institut Senckenberg, Frankfurt-am-Main, Germany. ZMA: Zoological Museum Amsterdam, The Netherlands.
Fig. 1. Ordination of species A and species B along the first two principal components, based on a PCA of the characters VENT, SUBC, TAIL and EYED.
TwoStep Cluster analysis split the sample into two clusters and validated the initial assignment of specimens to the two species (henceforth: species A and species B). The results of a PCA are shown in Figure 1. A plot of the number of ventral scales against eye-diameter is shown in Figure 2. Both figures demonstrate a clear separation between the two species.
The most prominent results of univariate confirmatory analyses are summarized in Table 2. Species A has a higher number of ventral scales, a higher average number of subcaudal scales and a smaller average eye-diameter. The relation between SVL and eye-diameter for the two species is depicted in Figure 3. With regard to coloration, a conspicuous character of species A is a bright interparietal spot which is absent in species B. However, several specimens constituted exceptions to this rule. In one specimen of species A (from Bombay, India) and two specimens of species B (from Sri Lanka), an interparietal spot was present but in a rudimentary (i.e. barely visible) form. Finally, species A has a substantially shorter vertebral stripe than species B.
Table 2. Descriptive statistics with regard to the most diagnostic characters of species A and B. Eye-diameter is SVL-adjusted (see Materials and Methods). Significance-levels are provided in the last column.
Sexual dimorphism in the diagnostic characters was not detected in either species, a finding that is largely in line with results regarding several congeneric species (How et al., 1996; Vogel and Van Rooijen, 2007; Van Rooijen and Vogel, 2008).
Eye-diameter, number of ventrals and number of subcaudals were subjected to analysis of geographical variation. This analysis was restricted to OTU’s from which both species had been sampled, thus excluding OTU 3 and OTU 4. Only the number of ventral scales was found to exhibit significant geographic variation (P = 0.01), although this variation is negligible in the context of interspecific differences (P < 0.000001). With regard to this character, the two species were found to differ slightly in their patterns of geographic variation based on a significant interaction OTU x species (P = 0.02).
The analyses demonstrate unequivocally that two species are currently referred to the binomial Dendrelaphis tristis. Dendrelaphis tristis was described by Daudin (1803) on the basis of information on a single specimen published by Russell (1796). Daudin did not deposit a type-specimen in a collection as was usual at that time. He mentioned 181 ventrals and 130 subcaudals, enlarged vertebral scales and a whitish-grey first dorsal scale row. The enlarged vertebral scales and the light first dorsal row are consistent with both species but the high ventral and subcaudal counts are only consistent with species A. Therefore, we refer species A to the name Dendrelaphis tristis (Daudin, 1803). The next available name according to the rule of priority is Dipsas schokari Kuhl, 1820. This name was synonymized with D. tristis by Boulenger (1894). Kuhl also did not assign a type-specimen, nor a type locality, but he provided ventral and subcaudal counts for five syntypes. The range of ventrals and subcaudals (168-183 and 111-131 respectively) given by Kuhl indicate that both species were included in his type-series. In his general description Kuhl mentioned a vertebral stripe, a light ventrolateral line, a postocular stripe and 5-6 temporal scales. These characters are also consistent with both species. Despite the fact that Kuhl’s name Dipsas schokari refers to both taxa and a type-specimen was not designated explicitly, the name is available according to the International Code of Zoological Nomenclature (ICZN, 1999). The fifth syntype mentioned by Kuhl agrees beyond doubt with species B. In Figure 4, the number of ventrals and subcaudals of the specimens examined for this study are plotted together with those of Daudin’s type of D. tristis and Kuhl’s fifth syntype of D. schokari. Figure 4 shows that Daudin’s type is situated within the area occupied by species A whereas Kuhl’s 5th syntype is positioned within the area occupied by species B. Indeed, Daudin’s type differs significantly from species B as the ventral and subcaudal counts differ more than 2.5 standard deviations from the respective means of species B. In a similar vein, Kuhl’s 5th syntype differs significantly from species A as its ventral count is situated further than 3 standard deviations from the mean of species A. As such, there is no doubt that Dendrelaphis tristis (Daudin, 1803) is the correct name for species A whereas Dipsas schokari Kuhl, 1820, in the combination Dendrelaphis schokari (Kuhl, 1820), should be adopted for species B.
Fig. 4. Plot of the number of ventrals against the number of subcaudals for species A and species B. Ventral and subcaudal counts of the holotype of D. tristis and the 5th syntype of D. schokari are included.
An excellent overview of the life and work of Heinrich Kuhl is provided by Klaver (2007). Heinrich Kuhl (1797-1821) studied natural sciences at the University of Groningen, The Netherlands from 1816 to 1819. In 1820 Kuhl was employed by the Dutch government and was sent to Java to study the natural history of this island. After reaching Java he died within a year.
Kuhl described Dipsas schokari while he studied at the University of Groningen. The types mentioned by Kuhl were part of his personal collection. He donated this collection to the museum of natural history of the University of Groningen when he departed to Java. Unfortunately, the collection of the museum of natural history of the University of Groningen was destroyed in a fire in 1906. The syntypes of Dendrelaphis schokari should be considered lost. In order to stabilize the names D. tristis and D. schokari as well as designate a type locality for the latter, we designate RMNH 842 as the neotype of Dendrelaphis schokari (Kuhl, 1820) and SMF 58442 as the neotype of Dendrelaphis tristis (Daudin, 1803) on the basis of article 75 of the ICZN. The type locality of Dendrelaphis schokari becomes Ceylon (now: Sri Lanka). The type locality of Dendrelaphis tristis becomes Calcutta, India.
Dipsas schokari Kuhl, 1820
Dendrophis helena Werner, 1893
Remarks. The synonymy-list is restricted to references in which data on numbers of ventral scales and subcaudal scales are given as these characters are diagnostic. Two currently recognized synonyms of D. tristis, Leptophis mankas (Bell, 1826) and Dendrophis maniar (Boie, 1827) can not be referred to either D. tristis or D. schokari and will be subjected to further research.
Material examined. Sri Lanka: NMW 23669:2, NMW 24382:2, NMW 24382:3, NMW 24382:4, MNHN 1890.0065, NMW 23669:1, RMNH 842, RMNH 7066 (1), RMNH 7066 (2), BMNH 19184.108.40.206, BMNH 1969.2781; SMF 62076, SMF 62074, SMF 18672, MHNG 1198.52, MTKD D 10646, MTKD D 10440, MTKD D 15438, MHNG 1199.57, MHNG 1198.54, SMF 70286, MHNG 762.73, MHNG 1198.51, MHNG 1198.55, MHNG 1198.53, MHNG 1198.50, SMF 32366, SMF 70285; India (Malabar Coast): MNHN 244; India (Kottayam, Travancore): BMNH 19220.127.116.11, BMNH 1918.104.22.168; India (Punkanaad, Travancore): BMNH 1922.214.171.124, BMNH 19126.96.36.199; unknown locality: RMNH 7081 (1), RMNH 7081 (2), RMNH 7081 (3), RMNH 7081 (4), RMNH 7081 (5).
Type locality (by designation of a neotype). “Ceylon”, now Sri Lanka.
Diagnosis. A species of Dendrelaphis, characterized by the combination of: (1) vertebral scales enlarged but smaller than the dorsals of the first row; (2) 155-177 ventrals; (3) 105-127 divided subcaudals; (4) 15 dorsal scale rows at midbody; (5) anal shield divided; (6) 1 loreal scale; (7) 2 supralabials touching the eye; (8) a short first sublabial that touches 2 infralabials; (9) 4 to 7 temporal scales; (10) 2 to 3 postoculars; (11) maximum total length 119.0 cm; (12) TAIL/TL 0.30-0.34; (13) an interparietal spot is absent (rarely rudimentarily present); (14) the presence of a light ventrolateral stripe; (15) the presence, in most specimens, of a vertebral stripe.
Description of the neotype. Adult female; SVL 51.0 cm; TAIL 22.5 cm; 161 ventrals (2 preventrals); 113 subcaudals, all divided; anal shield divided; 1 loreal scale (L+R); 9 infralabials (L+R); first infralabials touch at the mental groove; first sublabial touches infralabials 6 and 7 (L+R); 9 supralabials (L+R), supralabials 5 and 6 touch the eye (L+R); 2 postoculars (L+R); temporal formula: 2+2 (L+R); dorsal formula: 15-15-11; vertebral scales enlarged but smaller than the scales of the first dorsal row; width of the dorsal scale at the position of the middle ventral 2.1 mm; eye-diameter 4.9 mm (L+R); distance anterior border of eye to posterior border of nostril 4.5 mm (L+R); a dark postocular stripe starts behind the eye, covers only the lower quarter of the temporal region and ends at the edge of the jaw; a vertebral stripe, formed by yellow spots on the vertebral scales, starts behind the head and is no longer visible after the level of the 34th ventral scale; an interparietal spot is absent; a faint light ventrolateral line is present, not bordered by black lines; ground color brown, based on the color of unshed skin; supralabials and throat yellow; ventrals yellow anteriorly, yellowish-green posteriorly.
Variation and comparison with Dendrelaphis tristis (Daudin, 1803). Descriptive statistics with regard to D. tristis and D. schokari are provided in Table 3.
Sexual dimorphism. D. schokari exhibits sexual dimorphism in the number of dorsal scale rows one head-length before the anal shield (P < 0.00001, χ2 test). All male specimens have 9 dorsal scale rows at this position whereas 75% of the female specimens have 11 dorsal scale rows at this position.
Distribution. The examined specimens of D. schokari originated from Sri Lanka and the Western Ghats (South-West India), areas that have been shown to be biogeographically closely related (Das, 1995).
Coluber tristis Daudin, 1803
Dipsas schokari Kuhl, 1820 (part.)
Dendrophis scandens Boie, 1827
Dendrophis chairecacos Boie, 1827
Dendrophis boii Cantor, 1839
Material examined. Sri Lanka: BMNH 19188.8.131.52, BMNH 184.108.40.206, BMNH 1972.2183, ZMA 21563, SMF 18671, SMF 32367; India (Bengals): RMNH 843 (1), RMNH 843 (2), RMNH 843 (3), RMNH 843 (4), RMNH 843 (5); India (Calcutta): NMW 23686:6, NMW 23686:7, SMF 58442, SMF 58071; India (Darjeeling): BMNH 220.127.116.112, BMNH 1909.3.9.12; India (Bombay): ZMA 14120(2), BMNH 18.104.22.168, ZMA 14120(1); India (Madras): SMF 18634, SMF 18595; India (no exact locality): BMNH 22.214.171.124, MHNG 1553.8; Bengals/Myanmar: NMW 23669:5, NMW 23669:3.
Type locality (by designation of a neotype). “Calcutta, India” (original type locality: “Hyderabad”).
Diagnosis. A species of Dendrelaphis, characterized by the combination of: (1) vertebral scales enlarged but smaller than the dorsals of the first row; (2) 178-198 ventrals; (3) 121-136 divided subcaudals; (4) 15 (rarely 13) dorsal scale rows at midbody; (5) anal shield divided; (6) 1 loreal scale; (7) 2 supralabials touching the eye; (8) a short first sublabial that touches 2 infralabials; (9) 5 to 8 temporal scales; (10) 2 postoculars; (11) maximum total length 115.0 cm; (12) TAIL/TL 0.30-0.33; (13) a bright (rarely rudimentary) interparietal spot; (14) the presence of a light ventrolateral stripe; (15) the presence, in most specimens, of a vertebral stripe.
Fig. 11. Dendrelaphis tristis, Bombay, ZMA 14120(2), note the interparietal spot on top of the head.
Description of the neotype. Adult male; SVL 45.0 cm; TAIL 21.5 cm; 185 ventrals (2 preventrals); 134 subcaudals, all divided; anal shield divided; 1 loreal scale (L+R); 11 infralabials (L+R); first infralabials touch at the mental groove; first sublabial touches infralabials 6 and 7 (L+R); 9 supralabials (L+R), supralabials 5 and 6 touch the eye (L+R); 2 postoculars (L+R); temporal formula: 2+2+2 (L), 2+1+2 (R); dorsal formula: 15-15-9; vertebral scales enlarged but smaller than the scales of the first dorsal row; width of the dorsal scale at the position of the middle ventral 1.9 mm; eye-diameter 3.8 mm (L), 3.9 mm (R); distance anterior border of eye to posterior border of nostril 3.2 mm (L+R); a postocular stripe starts behind the eye and covers approximately 30% of the temporal region; a vertebral stripe, formed by a light colour of the vertebral scales and edges of adjoining dorsal scale rows, starts behind the head and is no longer visible after the level of the 17th ventral scale; an interparietal spot is present; a light ventrolateral line is present, bordered above by a thin dark line; ground color brown; supralabials, throat and ventral scales off-white.
Variation and comparison with Dendrelaphis schokari. Descriptive statistics with regard to D. tristis and D. schokari are provided in Table 3.
Sexual dimorphism. Like D. schokari, D. tristis exhibits sexual dimorphism in the number of dorsal scale rows one head-length before the anal shield (P = 0.0003, χ2 test). 85% of the females have 11 dorsal scale rows at this position whereas 90% of males have 9 dorsal scale rows at this position.
Distribution. The examined specimens of D. tristis originated from Sri Lanka, Western Ghats (Bombay), Eastern Ghats (Madras), Northeast India and Myanmar. Daudin’s type originated from Central India (Hyderabad). Boulenger (1894) provides a record from North-West India (Sind). His record is unambiguous given the mentioned ventral and subcaudal counts (185 and 127 respectively). According to Shrestha (2001), D. tristis also occurs in Nepal. Unfortunately, Shrestha did not provide diagnostic data on his record. However, the occurrence of D. tristis in Nepal is plausible given the verified presence of this species in North-East India. In summary, D. tristis ranges from Sri Lanka northward through most of India to Myanmar whereas the distribution of D. schokari is restricted to Sri Lanka and South-west India (Western Ghats) As such, D. schokari appears to have a limited distribution in comparison with D. tristis. This is in agreement with data provided by Boulenger (1894) and Wall (1909, 1921a, 1921b). These authors mention high ventral and subcaudal counts, consistent with D. tristis, for specimens from northern regions and mention both high and low ventral and subcaudal counts, consistent with a combination of D. tristis and D. schokari, for specimens from southern regions.
The close phenetic similarity between D. schokari and D. tristis indicates that these taxa are sister species, although a phylogenetic analysis should corroborate this. The interparietal spot, bright in D. tristis and rudimentary in some specimens of D. schokari, in particular suggests a close relationship. This conspicuous character is absent in all congeneric species and presumably represents an apomorphy within these two species. Although sympatric on Sri Lanka and the Western Ghats, these species probably do not occur syntopically. The fact that the distribution of D. schokari is restricted to Sri Lanka and the Western Ghats suggests that it is an inhabitant of tropical forest. The wide distribution of D. tristis in India on the other hand suggests an adaptation to relatively dry and open habitat. The difference in eye-size points in the same direction: the comparatively large eye of D. schokari presumably represents an adaptation to the lower light intensity prevalent in tropical forest habitat. D. schokari may have evolved allopatrically on Sri Lanka. The connections between Sri Lanka and India that came into existence due to Pleistocene lowering of sea levels (e.g. Voris, 2000; Pethiyagoda, 2005) could have enabled D. schokari to disperse into South India, at the same time enabling D. tristis to invade Sri Lanka from India.
The Western Ghats and Sri Lanka together have been designated as one of the biodiversity hotspots of the world (Mittermeier et al., 2005) and are known to host a high level of endemism among reptiles (e.g. Das, 1996; Ishwar et al., 2001; Mittermeier et al., 2005). Recent species descriptions suggest that biodiversity as well as levels of endemism harboured by these areas may be substantially higher than currently known (e.g. Pethiyagoda, 2005; Mendis Wickramasinghe et al., 2007; Mukherjee and Bhupathy, 2007). The resurrection of D. schokari from synonymy highlights the unique biological status of this area. Furthermore, it stresses the shortcomings in our current understanding of Dendrelaphis-systematics, as previously noted (Vogel and Van Rooijen, 2007; Van Rooijen and Vogel, 2008). The systematics of Dendrelaphis are still far from complete. For instance, Leptophis mankas (Bell, 1826) might represent a valid name as indicated in the results-section. Its status will be subjected to further research. One reason for the unsatisfactory status of Dendrelaphis-systematics lies in the fact that most prior taxonomic arrangements were based on rather crude as well as subjective judgements. For example, Meise and Henning (1932) recognized eight species and many subspecies but their criteria remained largely implicit. Since the last major revisions of the genus, the advent of computer-technology and associated development of advanced multivariate techniques have greatly improved possibilities for sophisticated and objective taxonomic analysis. Application of such new techniques will considerably refine the taxonomic dissection of this genus. In addition, the application of species concepts that, more than the biological species concept, reflect evolutionary history (e.g. Frost and Hillis, 1990; Zink and McKitrick, 1995; De Queiroz, 1998) may be expected to have a substantial impact on the systematics of this genus, especially with regard to allopatric populations.
We are grateful to Patrick David (Paris, France) for his critical reading of this manuscript and his constructive comments that greatly improved the draft of this paper. We thank Annemarie Ohler and Alain Dubois (Paris, France), Colin J. McCarthy (London, United Kingdom), Franz Tiedemann and Richard Gemel (Vienna, Austria), Koos van Egmond, Caroline Pepermans and Pim Arntzen (Leiden, The Netherlands), Ronald Vonk and Dik Iliohan (Amsterdam, The Netherlands), Gunther Köhler and Monika Laudahn (Frankfurt am Main, Germany), Uwe Fritz and Edgar Lehr (Dresden, Germany) and Andreas Schmitz (Genève, Swizerland) for their assistance in sending us or letting us examine preserved specimens. We thank Ruchira Somaweera (Kandy, Sri Lanka) for providing pictures of living specimens of Dendrelaphis schokari. Furthermore, the critical and constructive comments of Pim Arntzen and two anonymous reviewers contributed to the honing of the final text and we wish to thank them here. Last but not least, we are grateful to Hein van Grouw (Leiden, The Netherlands) for providing information on the work and collection of Heinrich Kuhl.
Received: 14 November 2007
Accepted: 8 February 2008
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