- Research article
- Open Access
Consuming viscous prey: a novel protein-secreting delivery system in neotropical snail-eating snakes
BMC Evolutionary Biology volume 14, Article number: 58 (2014)
Efficient venom delivery systems are known to occur only in varanoid lizards and advanced colubroidean snakes among squamate reptiles. Although components of these venomous systems might have been present in a common ancestor, the two lineages independently evolved strikingly different venom gland systems. In snakes, venom is produced exclusively by serous glands in the upper jaw. Within the colubroidean radiation, lower jaw seromucous infralabial glands are known only in two distinct lineages–the basal pareatids and the more advanced Neotropical dipsadines known as “goo-eating snakes”. Goo-eaters are a highly diversified, ecologically specialized clade that feeds exclusively on invertebrates (e.g., gastropod molluscs and annelids). Their evolutionary success has been attributed to their peculiar feeding strategies, which remain surprisingly poorly understood. More specifically, it has long been thought that the more derived Dipsadini genera Dipsas and Sibynomorphus use glandular toxins secreted by their infralabial glands to extract snails from their shells.
Here, we report the presence in the tribe Dipsadini of a novel lower jaw protein-secreting delivery system effected by a gland that is not functionally related to adjacent teeth, but rather opens loosely on the oral epithelium near the tip of the mandible, suggesting that its secretion is not injected into the prey as a form of envenomation but rather helps control the mucus and assists in the ingestion of their highly viscous preys. A similar protein-secreting system is also present in the goo-eating genus Geophis and may share the same adaptive purpose as that hypothesized for Dipsadini. Our phylogenetic hypothesis suggests that the acquisition of a seromucous infralabial gland represents a uniquely derived trait of the goo-eating clade that evolved independently twice within the group as a functionally complex protein-secreting delivery system.
The acquisition by snail-eating snakes of such a complex protein-secreting system suggests that the secretion from the hypertrophied infralabial glands of goo-eating snakes may have a fundamental role in mucus control and prey transport rather than envenomation of prey. Evolution of a functional secretory system that combines a solution for mucus control and transport of viscous preys is here thought to underlie the successful radiation of goo-eating snakes.
The origin and evolution of the venom-delivery system in snakes has been a subject of considerable debate [1–7]. Recent contributions were successful in providing new, stimulating insights on the long-standing problem of the origin of the ophidian upper jaw venom system [6, 7]. However, much remains to be elucidated regarding the function and morphological diversification of venomous systems in snakes [8–11]. Among advanced colubroids  the dipsadine “goo-eating” snakes are known to possess a peculiar lower jaw seromucous secreting system [10, 13–17] that may be paralleled only in pareatids, a basal lineage of snail-eating colubroideans that also seems to possess a similar (but not homologous) lower jaw seromucous system [8, 15, 16].
“Goo-eaters” were originally defined as a clade of eight Neotropical genera belonging to the Subfamily Dipsadinae . Among these, Adelphicos, Atractus, and Geophis are known to feed mainly on earthworms, whereas Ninia, Dipsas, Sibynomorphus, Sibon, and Tropidodipsas are molluscivorous specialists that feed mainly on slugs and snails (see Additional file 1). The latter four genera are often called “snail-eating” snakes . Chersodromus and three recently described genera–Chapinophis, Omoadiphas, and Plesiodipsas–also seem to belong to the goo-eating dipsadine snake assemblage [20–27]. However, virtually nothing is known about their relationships and feeding strategies due to their cryptic habits and scarcity in collections.
Our investigation of the cephalic glandular and muscular systems of snail-eating snakes revealed a novel lower jaw protein-secretion delivery system that we describe and compare with other goo-eater genera. The new system reported here represents the first protein-secreting apparatus in snakes that is not functionally related to a specialized tooth or tooth row, but rather opens loosely on the epithelium of the mouth floor. The acquisition by the derived snail-eating snakes of such a complex protein-secreting system suggests that the secretion from the hypertrophied infralabial glands of goo-eating snakes may have a fundamental role in mucus control and prey transport rather than envenomation of prey . Evolution of a functional secretory system that combines a solution for mucus control and transport of viscous prey is here thought to underlie the successful radiation of goo-eating snakes, a group that includes three of the most speciose genera of advanced snakes known so far.
The infralabial glands and the epithelium of the floor of the mouth of Dipsadini
In order to investigate the anatomical specializations of the protein-secretion delivery system associated to the lower jaw of snail-eating snakes, we analyzed representatives of four of the five known genera of Dipsadini. We also dissected representatives of five other goo-eating genera and 29 additional genera of Dipsadinae (see Additional file 2 and Methods).
All four available genera of Dipsadini present hypertrophied infralabial glands, a salient characteristic that distinguishes them from the remaining Dipsadinae. Besides being hypertrophied, the infralabial gland shows two distinct patterns within Dipsadini, as follows: in Sibon and Tropidodipsas (and in the goo-eaters Atractus, Adelphicos, and Ninia) the infralabial gland is single and located in the ventrolateral surface of the head, below the infralabial scales, whereas in Dipsas and Sibynomorphus it is divided in two distinct parts (Figures 1A,B,2A,B; Table 1). The divided infralabial gland in these two genera is composed of a thin stripe of gland that runs along the lip and below the infralabial scales, from the anterior tip of the dentary to the corner of the mouth (Figure 1A,B), and a much larger gland that runs along the ventrolateral surface of the mandible (Figures 1A,B, 2A,B).
We distinguish in the text below the more dorsolateral part of the infralabial gland from the more hypertrophied ventrolateral part, as the “mucous infralabial gland” (il1) and the “seromucous infralabial gland” (il2), respectively (Figure 3). In Dipsas and Sibynomorphus, the two portions of the infralabial gland are anteriorly connected through the glandular body and through a series of small ducts (Figure 3).
The epithelium of the floor of the mouth in Dipsadini is modified into a loose and extensively folded epithelial tissue that covers the whole oral cavity, being more accentuated in Dipsas and Sibynomorphus where a heavily folded epithelium accommodates the large muscle levator anguli oris laterally to the dentary (Figure 4). The floor of the mouth in most species of Dipsas and Sibynomorphus examined is also apparently unique in having a pair of openings at the level of the intermandibular raphe for the release of secretion coming from il2 through a single large duct (Figure 5; Table 1), also revealed by histological sections in D. albifrons and D. indica (Figures 6 and 7). We failed to confirm the presence of “mandibular ducts” in six species of Dipsas (D. brevifascies, D. pakaraima, D. temporalis, D. tenuissima) and one Sibynomorphus (S. vagus), although their presence could not be completely ruled out (Table 1).
The il1 of Dipsas and Sibynomorphus and the single infralabial gland of Sibon and Tropidodipsas are similarly connected with the mouth by short ducts along the margin of the lower lip, as in all other Dipsadinae. The short openings of the ducts of the il1 are similar in size and proportion in all Dipsadinae, except in Sibynomorphus and Crisantophis where they are significantly larger in diameter. The ducts of the il1 in Dipsadinae open inside a shallow gutter, or fold, that runs along the lower lip and sets the boundary between the soft epithelium of the mouth and the cornified infralabial scales (Figure 3). This fold is much more pronounced in all four genera of Dipsadini, and forms a deep gutter that tends to close dorsally by the contact of both margins. In Sibon and Sibynomorphus, a second deep fold with no ducts runs parallel to the latter, forming a double infolding along the margin of the lip (Figure 3) that was not observed in Dipsas and Tropidodipsas.
In all four genera of Dipsadini, the median tubercle is reduced in size, forming only a small, anteriorly tapering protuberance. The sublingual plicae are also poorly developed on the floor of the mouth and closely approach each other anteriorly due to the reduction of the median tubercle. The outer tongue sheath is reduced, and delineates a narrow opening for the tongue in Dipsas, while it forms a larger opening for the tongue in Sibon, Sibynomorphus, and Tropidodipsas (Figure 4). Sibon nebulatus differs from the other species analyzed in respect to the position of the larynx that is located more posteriorly on the floor of the mouth, being separated from the outer sheathing tongue by at least twice the distance than in other dipsadines (Figure 4C).
Histology and histochemistry of the infralabial glands of Dipsadini
Histological procedures were performed in adult individuals representing four genera of snail-eating snakes (Dipsas, Sibon, Sibynomorphus, Tropidodipsas) (see Additional file 2).
Infralabial glands are basically composed by the secretory portion forming the glandular body and by ducts in its interior. They are enveloped by a thin layer of connective tissue that penetrates the glandular body, dividing the gland in lobuli and involving all acini and ducts (Figures 8C and 9C). Due to the spatial arrangement of the two portions of the infralabial gland (il1 and il2) in the mandible, they are rarely seen simultaneously in a single histological section, justifying the need for serial sections in sagittal and horizontal planes that allow a three-dimensional interpretation of the structures.
In Dipsas albifrons, the posterior region of the il2 is composed only by seromucous cells, while the rest of the gland is composed of mucous cells (Figure 6A,B). The limit between these two regions is clearly visible through the contrasting stain of seromucous and mucous cells (Figure 6D). While seromucous cells react weakly positive to PAS and highly positive to bromophenol blue (Figure 6F and G, respectively), mucous cells show an intense positive reaction to alcian blue pH 2.5 and PAS (Figure 6E,F). The same pattern of cellular distribution is observed in D. indica (Figure 7A,C). Sections of the heads of both D. albifrons and D. indica reveal the presence of the mandibular duct that runs along the longitudinal middle of the il2, extending posteroanteriorly to open in the floor of the mouth at the level of the intermandibular raphe (Figures 6B,C and 7B,C and E). The duct is lined with a simple epithelium constituted by columnar mucous cells.
In Sibynomorphus mikanii, the il2 shows a simple epithelium with polygonal cells forming acini (Figure 8C). The lumen of these acini is very narrow and difficult to observe, being filled with secretion in the few histological sections where the structure is visible. The mandibular duct is clearly visible in a sagittal section of the lower jaw of S. mikanii (Figure 8C). The il2 of S. mikanii reacts positively to bromophenol blue. In S. mikanii and S. neuwiedi, the il1 shows a simple epithelium, with acini constituted mainly by mucous cells (Figure 8B,D,E). As shown in transversal sections of the head of S. neuwiedi, the il1 presents a series of short ducts that open just under the infralabial scales (Figure 8E,F).
Dipsas neivai also presents a large mandibular duct that runs along the longitudinal middle of the il2 (Figure 9A). However, none of the available sections provided a clear view of the opening of the duct at the level of the mouth floor. The il2 is composed by prismatic secretory cells arranged in acini, and its mandibular duct is lined by a simple columnar epithelium (Figure 9C). Cells lining both il1 and il2 ducts are always of mucous nature, reacting positively to PAS and alcian blue pH 2.5 (Figure 9E,F), while part of the cells forming acini react positively to bromophenol blue (Figure 9D), revealing their seromucous nature and another part is mucous, reacting positively to alcian blue pH 2.5 (Figure 9E).
In Sibon nebulatus, the infralabial gland is constituted by mucous and seromucous cells organized in tubules and acini (Figure 10A,B). The acini are observed in the posterior most portion of the gland and are mainly constituted by seromucous cells, being more intensively stained by hematoxylin-eosin and bromofenol blue. On the other hand, the tubules are mainly constituted by mucous cells that stain only with hematoxylin-eosin (Figure 10B,D,E). In the central region of the gland, a series of ducts extend along the glandular body, opening in the anterior region of the mouth (Figure 10C,G). In addition to these large ducts, a series of shorter ducts are arranged perpendicularly to the gland, opening more posteriorly, between the infralabial scales and the oral epithelium. Posteriorly, at the level of the insertion of the LAO into the gland, the ducts surround the muscle to reach the oral epithelium (Figure 10F).
In Tropidodipsas sartorii, the infralabial gland is mainly constituted by mucous cells that are arranged in acini and distributed along the whole body of the gland (Figure 11A). These mucous cells stain with hematoxylin-eosin and react positively to alcian blue pH 2.5 (Figure 11A,C). Only the posteriormost region of the gland presents a series of small acini that are composed by seromucous cells that stain only with hematoxylin-eosin (Figure 11D). The infralabial gland of T. sartorii has a large duct that extends along its medial surface, reaching its anterior portion (Figure 11A). This duct is formed by the confluence of a series of shorter and smaller converging ducts and does not correspond to the mandibular duct of il2 (Figure 11A,B). Both larger and smaller ducts are constituted by cells with low cytoplasm and several nuclei, resembling a stratified epithelium (Figure 11B).
Muscles associated with the infralabial glands of Dipsadini
In all Dipsadini, both levator anguli oris (LAO) and intermandibularis posterior pars posterior (IPP) muscles were observed to be closely associated with the infralabial glands, being adpressed to the wall of the gland or attached to it as a compressor of the gland (Table 1). The relation between these muscles and the infralabial glands il1 and il2, the lower jaw, and the corner of the mouth are described below.
The LAO of Dipsadini is always functionally and morphologically distinct from the adductor mandibulae externus superficialis muscle (AES; sensu Zaher ), and are treated here as two separate muscular units . The well-developed LAO of goo-eating snakes is innervated by its own anterior branch of the ramus mandibularis of the trigeminal nerve . Among all adductores externi muscles, only the LAO is directly associated with the infralabial glands in snail-eating dipsadines.
The LAO of Dipsadini is a long, parallel fibered muscle that extend from behind the eye to the anterior half of the lower jaw, curving around the angle of the mouth to insert on the mandible or on the surface of the il1. The anterolateral surface of the epimysium is always firmly attached to the buccal membrane of the corner of the mouth. Except for these few characteristics, the LAO showed significant variation among studied genera, being completely differentiated from the AES in all goo-eaters, except in Tropidodipsas, Sibon, and Atractus in which some of the more posterodorsal fibers tend to share an aponeurosis with the more anteromedial fibers of the AES (Figure 1).
The LAO is anterior to the AES in Dipsas, Sibynomorphus, and Atractus. In two species of Atractus (A. major and A. flammigerus), the posteriormost fibers of the LAO are medial to the AES (Figure 12A). In Ninia, Chersodromus, and Geophis, the anterior half of the LAO is anterior to the AES while the posterior fibers broadly overlap the anterior half of the AES at their origin. The LAO is medial in Sibon and Adelphicos (Figures 1C, 12B). In Tropidodipsas, the two species examined showed distinct arrangements, the LAO being lateral to the AES in T. fischeri and medial in T. sartorii (Figure 1).
In all species of Dipsas examined, the origin of the LAO is very large, encompassing the entire postocular region laterally. Three distinct conditions are found in Dipsas. In Dipsas incerta, D. brevifascies, and D. temporalis, the LAO arises from the entire laterodorsal surface of the postorbital. The postorbital bone is long, reaching the ectopterygoid ventrally. In Dipsas bucephala, D. indica, D. catesbyi, and D. albifrons, the origin of the LAO extends from the base of the postorbital to the lateral tip of the maxillary ramus of the ectopterygoid. Dipsas neivai shows the largest condition, with the LAO extending from the base of the postorbital to the posterolateral edge of the maxilla, and also encompassing the lateral tip of the maxillary ramus of the ectopterygoid. The postorbital being vestigial in D. neivai, the origin of the LAO is mostly on the posterior surface of a well-developed maxillo-postorbital ligament (Figure 1A).
The LAO integrally covers the Harderian gland, except in D. brevifascies where the gland is visible ventrally to the LAO. After curving the angle of the mouth, the LAO extends anteriorly to reach the anteriormost region of the dentary where the bundle ends in a broad aponeurosis that attaches to the ventrolateral edge of the anterior one-third of the dentary. The muscle does not insert broadly on the fascia of the infralabial gland, although it is somewhat tied by its fascia to the dorsal surface of the gland. In all species of Dipsas examined, the ventral (mandibular) portion of the LAO is visible dorsally to the il2, except in D. brevifascies where the muscle is completely covered by the infralabial gland. At the level of the anterior one third of the dentary, the il2 expands to the labial edge, covering the anterior tip of the bundle and its aponeurosis.
The LAO in Sibynomorphus is also greatly developed. In two of the eight species examined (S. mikanii and S. neuwiedi), the LAO arises via a large aponeurosis from the anterior half of the dorsolateral ridge of the parietal, extending to the distal tip of the postorbital and lateral tip of the maxillary ramus of the ectopterygoid (Figures 1, 2). The Harderian gland is visible medially to the aponeurosis in both species. In S. ventrimaculatus, the aponeurotic sheet is reduced and the fibers of the LAO cover completely the Harderian gland. In S. vagus and S. turgidus, the origin of the LAO is less extensive, arising only from the base of the postorbital and extending ventrally to the lateral tip of the maxillary ramus of the ectopterygoid. As in Dipsas, the LAO of Sibynomorphus curves around the corner of the mouth, forming a funnel-shaped bundle that inserts via an extensive aponeurosis to the ventrolateral edge of the anterior one-third of the dentary.
The LAO differs greatly in the two species of Tropidodipsas examined. In T. sartorii, the origin of the muscle is medial to both AES and Harderian gland (Figure 1D). On the other hand, T. fischeri shows the opposite condition, with a LAO clearly lateral to the AES and Harderian gland. In the former species, the origin of the muscle is confined to a narrow area; the fibers arise from the posteromedial base of the postorbital and adjacent surface of the parietal, below the anterior fibers of the AES. Both posterolateral fibers of the LAO and anteromedial fibers of the AES arise from a short aponeurosis. After originating medially to the AES, the LAO of T. sartorii takes an anterior position to the latter, extending ventrally towards the corner of the mouth (Figure 1D). In T. fischeri, the LAO arises from the anteriormost surface of the dorsolateral crest of the parietal, extending on the dorsolateral surface of the proximal half of the postorbital. The posteriormost fibers of the LAO and the anterior fibers of the AES arise from a common aponeurosis. In both species, the LAO forms a fusiform bundle at the level of the corner of the mouth that curves around the latter and inserts on the dorsal surface of the posterior third of the infralabial gland. Some of the more dorsal fibers are longer and converge to insert on a thin tendon that extends anteriorly in parallel to the dorsal edge of the infralabial gland. The tendon attaches to the skin below the infralabial scales.
The position of the LAO in Sibon is virtually the same as in Tropidodipsas sartorii, except in S. sanniolus in which the more lateral and anterior fibers arise from an aponeurosis shared with the anterolateral fibers of the AES and from the lateral surface of the postorbital, respectively. These fibers are thus anterior to the AES. However, the medial fibers that represent most of the mass of the LAO in S. sanniolus, remain medial to the AES.
In all four genera of Dipsadini examined, the IPP originates on the lateral surface of the compound bone, at the level of the mandibular fossa. It is a thin muscle that extends anteriorly, superficial to the neurocostomandibularis muscle and in parallel to the mandible, to attach to the skin lateral to the mental region but medially to the infralabial gland (Figure 2). Both bundles of the IPP do not meet on the midline ventrally. Instead, they are closely associated to the fascia of the infralabial gland, in which the more lateral epimysium of the muscle attaches. In a few specimens of D. neivai, a significant part of the muscle overlaps the infralabial gland and may act as a compressor of the gland since the epimysium of the muscle tends to fuse with the fascia covering the gland. In both Dipsas and Sibynomorphus (except S. neuwiedi), in which the mental groove is lost, we observe an unusual condition of the bundles pertaining to the muscle intermandibularis anterior pars posterior, which are divided in small groups of fibers that are interlaced at the level of the ventral midline (Figure 2A,B).
The muscles LAO and IPP in the remaining goo-eating snake genera Adelphicos, Atractus, Geophis, Ninia, and Chersodromus
In all species of Atractus examined, the LAO is anterior to the AES, except for the posteriormost fibers arising from the dorsolateral ridge of the parietal that are medial to the AES (Figure 12A). The LAO is a thin band of muscle arising from a narrow site of origin, which encompasses the posterolateral edge of the proximal half of the postorbital and anteriormost portion of the dorsolateral ridge of the parietal, just posterior to the postorbital-parietal contact. The LAO extends on a ventral and slightly posterior direction, curving around the corner of the mouth and inserting on the dorsal surface of the posterior third of the infralabial gland.
In Adelphicos veraepacis, the origin of the LAO is medial to the AES, arising from the anteriormost portion of the dorsolateral ridge of the parietal and the posterolateral margin of the short postorbital. The muscle extends ventrally and slightly posteriorly as a thin band of fibers, curving around the corner of the mouth and inserting on the dorsal surface of the posterior third of the infralabial gland (Figure 12B).
In all species of Geophis examined, the LAO corresponds to a thin, triangular sheet of muscle with an origin on the dorsolateral ridge of the parietal and postorbital, from the anterior edge of the muscle adductor mandibulae externus profundus (AEP; sensu Zaher, ) to the tip of the postorbital (Figure 12C). The posterior half of the LAO arises via an aponeurosis that overlies the dorsal portion of the AES. The fibers are directed dorsoventrally, converging to form a fusiform bundle at the level of the corner of the mouth. The site of insertion varies among the species examined. In G. anocularis, G. rhodogaster, G. dubius, and G. hoffmanni, the muscle terminates in an aponeurosis that inserts on the buccal membrane and lateral surface of the dentary dorsomedially to the infralabial gland. The epimysium of the LAO tends to be firmly attached to the dorsal surface of the posterior region of the infralabial gland. In G. brachycephalus and G. zeledoni, the muscle inserts broadly on the dorsal and dorsomedial surfaces of the posterior region of the infralabial gland (Figure 12C). The variation regarding the insertion site of the LAO seems to be correlated with the glandular differentiation present on the posterior region of the infralabial gland. In G. brachycephalus and G. zeledoni, where the LAO inserts on the infralabial gland, the gland shows two distinct anterior and posterior regions externally that are easily distinguished by their color and celular types.
The LAO of Ninia resembles the condition found in Geophis, with the significant difference that the muscle does not insert on the infralabial gland (except in one specimen of N. maculata and one of N. atrata in which the more lateral fibers insert on the dorsolateral surface of the gland). The LAO is a thin band of muscle originating on the dorsolateral ridge of the parietal and postorbital, from the middle of the AES to the proximal dorsolateral surface of the postorbital. The posterior half of the muscle overlaps the anterior half of the dorsal portion of the AES. Fibers extend ventrally to curve around the corner of the mouth and converge to terminate on a broad aponeurosis that attaches to the lateral surface of the dentary. The LAO of Chersodromus shows the same condition of Ninia (Figure 13A,C).
In the goo-eating snakes Adelphicos, Atractus, Geophis, Ninia, and Chersodromus, the IPP originates on the lateral surface of the compound bone, passing anteromedially as a thin bundle to attach to the ventral surface of the skin posteriorly to the mental region, with only some fibers reaching their counterpart at the midline. The epimysium of the muscle does not contact the infralabial gland.
Phylogenetic relationships of Dipsadinae
Our hypothesis of dipsadine interrelationships is based on Maximum Likelihood (ML) and Bayesian (BI) analyses of 576 sequences from five mitochondrial and six nuclear genes in 87 terminal taxa (including 26 outgroup and 61 ingroup taxa; see Materials and Methods). Our study included a substantially denser sample of dipsadine species compared to previous ones [29–31]. The extended dipsadine sampling is meant to provide a thorough test of the monophyly of the tribe Dipsadini, thereby offering a more rigorous background for the resulting hypothesis of interrelationships of its constituent parts.
Both ML (-lnL = -65357.67; Figure 14) and BI trees (majority rule consensus of 8500 trees after the burn-in; Figure 15) yield very similar results, differing only in the position of Tretanorhinus variabilis, Trimetopon gracilis, Nothopsis rugosus, and in the affinities between some species within the genera Atractus and Dipsas (see Additional file 3 and Additional file 4 for the complete tree topologies, including all outgroup taxa). We retrieved only 20 well-supported clades (i.e., BML and BPP frequencies of 70% and 0.8 or more, respectively), which correspond to only 33% of all possible clades. Most higher and lower-level interrelationships are not strongly supported, with the notable exception of the subfamily Dipsadinae (Figures 14, 15). Both ML and BI analyses recovered a well-supported Dipsadinae with a BML of 87% and a BPP of 1.0. Tantalophis discolor is positioned as the sister group of all other dipsadines , with low BML (<70%), but high BPP (0.93), and Amastridium veliferum, Coniophanes fissidens, and the genus Rhadinaea form a poorly supported clade (BMF < 70% and BPP < 90%) that represents the sister group of the remaining dipsadines. Within that clade, Coniophanes fissidens is retrieved as the sister group of the genus Rhadinaea, represented in this analysis by R. flavilata and R. fulvivittis. These two clades are poorly supported in both analyses (BML <70% and BPP <90%).
Both analyses recovered a poorly supported clade (BML <70%; BPP <0.8) grouping the remaining dipsadines distributed in five larger assemblages: 1) “Clade A”, formed by the genera Nothopsis, Imantodes, and Leptodeira; 2) “Clade B”, composed by Trimetopon and the “nightsnakes” genera Hypsiglena and Pseudoleptodeira; 3) “Clade C”, formed by Adelphicos quadrivirgatus, Hydromorphus concolor, and Tretanorhinus nigroluteus; 4) “Clade D”, composed by the goo-eaters Geophis and Atractus; 5) and “Clade E”, including Ninia and the snail-eating snakes Tropidodipsas, Dipsas, Sibon, and Sibynomorphus. Clades A, B, and D were retrieved with very low BML and BPP supports (<70%/<0.8), while Clades C and E received low to moderate BML (<70% and 70%, respectively) but high BPP supports (0.88 and 1.0, respectively). The genera Tretanorhinus, Imantodes, Geophis, Dipsas, and Sibynomorphus are not non-monophyletic in both ML and BI analyses, and Hypsiglena appears as non-monophyletic in the ML analysis. The genera Rhadinaea, Leptodeira, and Atractus are recovered as monophyletic in both analyses, but only Atractus receives moderate BML and high BPP support values (72%/1.0).
Within Clade A, Nothopsis rugosus is recovered as the sister group of a monophyletic tribe Imantodini (sensu Myers ) in the ML analysis, whereas in the BI analysis Nothopsis appears nested within the latter as the sister group of Imantodes inornatus. The genus Leptodeira is recovered as monophyletic, albeit with weak support. Similarly, within Clade B, Trimetopon gracile is found nested inside the night-snake genus Hypsiglena in the ML analysis, whereas in the BI analysis it clusters with Pseudoleptodeira nigrofasciata as the sister group of a monophyletic Hypsiglena.
Tretanorhinus variabilis clusters as the sister group of Clade A in the BI analysis whereas in the ML analysis it is placed as the sister group of a weakly supported clade formed by Clades B, C, D, E, and Cryophis.
Surprisingly, Cadle and Greene’s  goo-eating snakes are recovered as a polyphyletic assemblage in both analyses, with Adelphicos quadrivirgatus included in Clade C as the sister group of Hydromorphus concolor and Tretanorhinus nigroluteus, whereas the remaining goo-eating genera (Clades D and E) cluster together forming a clade that shows low BML support (<70%) but high BPP support (0.98). However, although our molecular tree points to a polyphyletic goo-eating assemblage, weak support for the nodes separating Adelphicos from the other goo-eaters and the expressive amount of morphological traits shared by both groups suggest caution interpreting these results. Within Clade C, H. concolor and T. nigroluteus form a monophyletic group of Central American aquatic snakes  strongly supported by both BML and BPP values (100/0.88). Clade C appears in both analyses as the sister group of the weakly supported clade formed by Cryophis and Clades D and E.
Cryophis hallbergi is recovered in both analyses as the sister group of a clade formed by the remaining goo-eating genera Ninia, Atractus, Geophis, Dipsas, Sibynomorphus, Sibon, and Tropidodipsas, albeit with weak support (<70%/<0.8). The latter clade is recovered with low BML (<70%) but high BPP (0.98) support values. Within that clade, very few nodes enjoy high support values and each probabilistic approach obtained a unique topology. However, some relationships are corroborated by both analyses. As previously shown by Grazziotin el al. , the goo-eating genera Ninia, Atractus, Geophis, Dipsas, Sibynomorphus, Sibon, and Tropidodipsas form two monophyletic assemblages: Clade D, composed by the genera Geophis and Atractus with low support values (<70%/<0.8), and Clade E composed by Ninia, Dipsas, Sibynomorphus, Sibon, and Tropidodipsas with moderate to high support values (70%/1.0). In both analyses, monophyly of Geophis is not recovered, with Geophis godmani and G. carinosus positioned as successive sister groups of Atractus. Monophyly of Atractus is retrieved with moderate to high support values (72%/1.0), although the relationship among the species of the genus received low support in both analyses. Ninia atrata is positioned as the sister group of Dipsadini, with the latter receiving surprisingly low support (<70%/<0.8). Within the tribe Dipsadini, Sibon nebulatus and Tropidodipsas sartorii form a moderately well supported clade (70%/0.92) that is retrieved as the sister group of a clade composed by Dipsas and Sibynomorphus. The latter clade is obtained in both analyses, with low BML (<70%) but high BPP (0.98) support values, and recovers both Dipsas and Sibynomorphus as paraphyletic in respect to each other. Within that paraphyletic assemblage, the following well-supported clades are present in both analyses: 1) Sibynomorphus turgidus and S. mikanii (78%/1.0), 2) Dipsas neivai and D. variegata (99%/1.0), 3) S. garmani and S. neuwiedi (100%/0.99).
The subfamily Dipsadinae is a well-corroborated monophyletic group of Neotropical snakes that has been recently redefined on the basis of both molecular and morphological evidence . However, affinities among dipsadine genera are still largely unknown . Some authors suggested monophyletic groups within this lineage, such as the “niniiforms” , the Leptodeira-Eridiphas, and the Sibon-Geophis clades . Recently, Mulcahy  provided molecular evidence for a clade including the nightsnakes Eridiphas, Hypsiglena, and Pseudoleptodeira, and another clade containing the genera Leptodeira and Imantodes. Mulcahy’s clade of nighstsnakes is recovered in our phylogenetic analysis with the genus Trimetopon nested within, although with low support (Figures 14 and 15).
According to Savitzky , the “niniiform” clade includes the genera Amastridium, Chersodromus, Diaphorolepis, Emmochliophis, Ninia, Nothopsis, Synophis, and Xenopholis. Recent molecular analyses pointed out the polyphyletic nature of niniiforms, with at least Ninia, Xenopholis and Nothopsis nesting distantly from each other within the dipsadid radiation [12, 29–31]. Cadle and Greene  were the first to explicitly suggest a close affinity of Ninia with the tribe Dipsadini, by recognizing a putative clade of seven Central American xenodontine genera of goo-eating snakes that feed exclusively on soft-bodied invertebrates. Interestingly, recent phylogenetic analyses have shown Ninia invariably nested within the Tribe Dipsadini, suggesting a paraphyletic condition for the tribe [12, 29, 30]. However, our analysis retrieved a monophyletic Dipsadini, with Ninia positioned outside the latter clade. This result is congruent with the morphological evidence at hand, since Ninia lacks the specializations shown by Dipsadini although most species are known to feed mainly on slugs  (Additional file 1).
Surprisingly, Cadle and Greene’s  goo-eating snakes were recovered as a polyphyletic assemblage in our analysis, with the cryptozoic Adelphicos clustering outside the clade formed by the remaining goo-eaters (i.e., Atractus, Geophis, Ninia, Dipsas, Sibon, Tropidodipsas, and Sibynomorphus), as the sister group of Hydromorphus and Tretanorhinus (Clade C in Figure 14). The latter two genera form a strongly supported clade of Central American aquatic snakes . Pyron et al. , who included Adelphicos for the first time in a molecular phylogenetic analysis, found the same clade formed by Adelphicos, Hydromorphus, and Tretanorhinus, but did not comment on this unexpected result. Our larger sample of Dipsadines failed to support a phylogenetic affinity of Adelphicos with the other cryptozoic goo-eating snakes traditionally associated with it (Atractus and Geophis), suggesting that their specialized feeding habits and morphology evolved independently within Dipsadinae (Figures 14 and 15).
Our results also suggest that the loss of grooved enlarged maxillary teeth and loreal scales, pointed out as evidence in support of the monophyly of the goo-eaters , should also be considered homoplastic in Adelphicos. However, although our molecular tree points to a polyphyletic goo-eating assemblage, weak support values for the nodes separating Adelphicos from the other goo-eaters and the expressive amount of morphological traits shared by both groups indicate that these results are still tentative.
The remaining goo-eating snakes form a moderately supported clade (Figures 14, 15) with low BML but high BPP support values. This monophyletic component, numbered 1 in Figure 14, includes the genera Geophis and Atractus, on the one hand, and Ninia, Tropidodipsas, Sibon, Dipsas, and Sibynomorphus, on the other. Both monophyletic components are described as Clades D and E in our Results, and are depicted in green and blue in Figure 14, respectively. While Clade D is formed by cryptozoic species that feed mainly on earthworms, Clade E (including Ninia) is essentially terrestrial or arboreal and known to be mainly molluscivorous (Additional file 1).
However, with the exception of Sibynomorphus, there have been reports of non-molluscan prey being extensively consumed in captivity or found in stomach contents and fecal samples of species from the remaining four genera in Clade E . Non-molluscan prey items comprise earthworms (in Dipsas bucephala, D. elegans, Ninia sebae, Sibon annulatus, S. argus, S. faciata, S. longifrenis, Tropidodipsas fisheri, T. philippii), arthropod remains (in Dipsas catesbyi, D. indica), leeches (in Ninia sebae), amphibian eggs (Sibon longifrenis and S. argus), and Amphisbaenidae (Ninia sebae) (Additional file 1). On the other hand, genera in Clade D seem to feed mainly on earthworms (Additional file 1). Nonetheless, some authors also described the presence of arthropod remains in the stomach content of Geophis incomptus (and there are indications that this seems to be a common item in several species of Atractus), acari (in Atractus latifrons and A. torquatus), slugs (in Atractus carrioni, G. nigrocinctus, and G. pyburni), leeches (in G. nasalis), and vertebrate remains such as lizards scales (in A. pantostictus) (Additional file 1).
Although the large number of specializations found in snail-eating snakes associated with molluscivory points to a single acquisition from a common ancestor , a closer inspection of the anatomy of these snakes suggests a more complex evolutionary scenario. In the phylogenetic tree depicted in Figure 14, three arrows, numbered from 1 to 3, indicate the nodes in which key evolutionary novelties arose within the goo-eating radiation and led to the highly specialized protein-secreting delivery system described herein in snail-eating snakes. Some of these novelties also seem to have appeared homoplastically in the cryptozoic genera Adelphicos and Geophis (arrows with an asterisk in their numbers in Figure 14) .
According to our dissections and based on the phylogenetic hypothesis in Figure 14, a fully individualized LAO that attaches ventrally to an enlarged and partially seromucous infralabial gland evolved independently in the genus Adelphicos (Arrow 1*) and in the common ancestor of the remaining goo-eating snakes, indicated by Arrow 1 in Figure 14, allowing these snakes to secrete and discharge mainly protein secretions into their mouth and prey. The clade Dipsadini, shown by Arrow 2 in Figure 14, is characterized by an hypertrophied LAO and an extensively folded and loose epithelial tissue covering the floor of the mouth, two synapomorphies that confer more flexibility and strength to mandibular movements. Arrow 3 corresponds to the node of the common ancestor of the genera Dipsas and Sibynomorphus, in which evolved a divided infralabial gland with a reduced il1 and a distinct, well developed il2 that discharges its protein secretion through a single large duct opening in the epithelium of the mouth floor at the level of the intermandibular raphe, an extended LAO that inserts via an aponeurotic tendon on the lateral surface of the tip of the dentary, and a heavily folded epithelium that accommodates the large LAO laterally to the dentary. Two distinct infralabial portions (il1 and il2) also evolved independently in the genus Geophis as depicted in Figure 14 (Arrow 3*). However, the condition in Geophis shows several important differences from the one described in Sibynomorpus and Dipsas, the more important ones being that the larger medial duct in the il2 of Geophis represents a real lumen that accumulates secretion and the muscle compressing the il2 corresponds to the muscle adductor mandibulae externus medialis pars posterior (AMEM, sensu Zaher ) instead of the IPP or LAO . The paraphyletic condition of Geophis shown in our phylogenetic analysis may suggest that the divided condition of the infralabial gland and specializations of the il2 in that genus were secondarily lost in Atractus. However, we suspect that a better sampling of Geophis will likely alter this result, and prefer to view any conclusion regarding this group as premature.
Although chemical properties and some anatomical aspects of the secretion delivery mechanism in Dipsadini could be inferred from the histological, morphological, and behavioral data, the exact role of the Dipsadini infralabial secretion and its use during predation in molluscs and other invertebrates is still largely unknown. Several authors hypothesized that toxins secreted by the infralabial glands of Dipsadini are probably used in some envenomation function or in assisting in the detachment of the snails from their shells [10, 14, 38, 39]. However, as shown by Sazima  and here (video provided as Additional file 5), Dipsas and Sibynomorphus always extract the snail through a sudden strike followed by a sequence of fast alternating insertions of the mandible inside the shell that are meant to rapidly extract the snail and ingest it in the same sequence (; Additional file 5). Such burst of mandibular movement results in a fast mechanical extraction that does not seem to depend on a chemical reaction of any kind. Similarly, observations made with species of the cryptozoic genus Atractus have shown that these snakes capture and ingest their prey through a sequence of fast, alternating movements of their mandible and do not seem to depend on any chemical aid from the protein secretion of the infralabial glands to subdue their prey.
As in Geophis, the presence of a seromucous il2 that is not functionally associated to a specialized tooth row but rather opens loosely in the epithelium of the mouth suggests a function that is likely to be directed to mucus control and prey ingestion rather than prey envenomation. Such function may have evolved associated to a seromucous condition of the infralabial gland il1 in the common ancestor of goo-eating snakes as a system to control unusual flow of mucus and assist in the ingestion of elongate, flexible and highly viscous preys (Figure 14). Evolution of a secretory system specialized in mucus control and prey ingestion, instead of simple prey envenomation, is here thought to represent a key element for the success of goo-eating snakes in the Neotropics.
We used throughout the text the term “snail-eating snakes” to refer to the tribe Dipsadini that comprises the genera Dipsas, Sibon, Sibynomorphus, Plesiodipsas, and Tropidodipsas, and the term “goo-eating snakes” to refer to the larger group that comprises the snail-eating snakes and the genera Adelphicos, Atractus, Chapinophis, Chersodromus, Geophis, Ninia, and Omoadiphas[18, 20]. The term “goo-eating snakes” will be used only for convenience since it appears to represent a paraphyletic lineage. Also, monophyly of Tropidodipsas is still controversial . However, we followed Wallach  that resurrected Tropidodipsas to accommodate five species (annulifera, fasciata, philippii, sartorii, and zweifeli) previously referred to Sibon. We also recognize herein the subfamily Dipsadinae as defined by Zaher et al. .
Representatives from four of the five known genera of Dipsadini were analyzed. Only Plesiodipsas was not available for dissection. However, Harvey et al.  provided descriptions of the head muscles and glands of the species. We dissected the head of 16 species of Dipsas, five Sibon, eight Sibynomorphus, and two Tropidodipsas, totalling 31 species of Dipsadini (see Additional file 2). Additionally to the “snail-eating” taxa, we also dissected 32 species of the goo-eating genera Adelphicos, Atractus, Chersodromus, Geophis, and Ninia, as well as 31 representatives of 29 additional genera of Dipsadinae (see Additional file 2).
All dissections and drawings were performed under a dissecting microscope Olympus SZX 12 equipped with a camera lucida. Specimens dissected in this study belong to the following collections: American Museum of Natural History, New York (AMNH); Instituto Butantan, São Paulo (IBSP); Museu Ecuatoriano de Ciencias Naturales, Quito (MECN); Museu Paraense Emílio Goeldi, Belém (MPEG); Museu de Zoologia da Universidade de São Paulo (MZUSP); Museum of Natural History, University of Kansas, Lawrence (KU); Museum of Natural Science, Louisiana State University, Baton Rouge (LSUMZ); National Museum of Natural History, Washington (USNM); Royal Ontario Museum (ROM).
Studies on the superficial soft tissue morphology of the mouth in snakes are scarce and have been directed to the palate rather than the floor of the mouth. McDowell  and Groombridge  offered some information on the soft tissue anatomy of the floor of the mouth of snakes, and we follow here their terminology. Glandular terminology follows Taub , Kochva , and Underwood . Terminology for the muscles of the intermandibular region of snakes follows Langebartel  and Groombridge . Terminology for the adductores externi muscles is still in dispute among authors [28, 45, 46]. We follow here the arrangement suggested by Zaher .
Molecular phylogenetic analysis
Our data matrix was composed by 87 terminal taxa and 501 sequences downloaded from GenBank for five mitochondrial (12S, 16S, cytb, nd2, nd4) and six nuclear genes (bdnf, c-mos, jun, nt3, rag1, rag2) (see Additional file 6 for Genbank accession numbers). When multiple sequences were available in GenBank for a given taxon, the most complete sequence was selected for inclusion. We also produced 75 additional sequences aiming to improve the completeness of our matrix. We used 26 outgroup terminals (19 Xenodontinae, three Carphophiinae, and three Natricidae). Sixty-one Dipsadinae terminals composed the ingroup, representing an increase of 25 species in respect to the taxon sampling used by Pyron et al.  and 31 species to the one used by Grazziotin et al. .
Primers and PCR protocols for partial amplification of genes 12S, 16S, cytb, bdnf, and c-mos were those described in Grazziotin et al. . We used the primers and protocols described in Vidal and Hedges , Noonan and Chippindale , and Chiari et al.  to amplify fragments for the nuclear genes jun, nt3, and rag1, respectively. PCRs were purified with shrimp alkaline phosphatase and exonuclease I (GE Healthcare, Piscataway, NJ, USA) and sequences were processed using the DYEnamic ET Dye Terminator Cycle Sequencing Kit in a MegaBACE 1000 automated sequencer (GE Healthcare) following the manufacturer’s protocols. Both strands were sequenced for all fragments and sequences were assembled using Geneious 5.5 .
The multiple sequence alignment process implemented in MAFFT  was applied for the rRNA sequences using the iterative refinement method implemented in the E-INS-I algorithm . Otherwise, all sequences for the coding genes were translated to amino acids and aligned based on the Gonnet series matrix implemented in Clustal X , and subsequently retro-translated to nucleotides. We concatenated the rRNAs with the retro-aligned coding genes, totalizing 9169 bps. All gaps were coded as missing data.
The concatenated matrix was analyzed by maximum likelihood (ML) and Bayesian inference (BI). We followed Grazziotin et al.  and split our matrix to allow the use of different model parameters for each codon position for the coding genes, and for each rRNA sequence. We carried out the ML analysis using RAxML 7.2.8 . The GTRGAMMA model was used for all partitions, as recommended in the program documentation. Forty RAS were built and the trees were swapped using LSR algorithm. To access the bootstrap frequencies for the ML analysis (BML), one thousand pseudoreplications of non-parametric bootstrap were performed using the Cluster hosted at the Laboratório de Alto Desempenho – Pontifícia Universidade Católica do Rio Grande do Sul (LAD-PUCRS). We used MrBayes 3.1.2  to implement BI analyses. Two independent runs with 11 million generations for four chains with a temperature of 0.05 were performed, sampling each 1000th generation. The prior probability densities for substitution rates and for stationary nucleotide frequencies of the rate matrix were selected as suggested by the MrModeltest analysis. A uniform prior was set for topology and the default unconstrained exponential prior was set for branch length parameter. Only the topology and branch lengths were treated as linked parameters among partitions. The log likelihood trace was accessed using Tracer v1.5  and the cutoff for the burn-in was determined as the point at which the trace became stationary. We accessed the average standard deviation of split frequencies to assure the convergence between different MrBayes runs and the Effective Sampling Sizes (ESS) for each parameter were inspected using the program Tracer. A 50% majority-rule consensus tree was constructed using the software TreeAnnotator v.1.5.4 . Frequency of nodal resolution for each clade was termed a Bayesian Posterior Probability (BPP).
Histology and histochemistry
Histological procedures were performed in 28 adult individuals belonging to the snail-eating genera Dipsas, Sibon, Sibynomorphus, Tropidodipsas and the remaining goo-eating genera Atractus, Geophis, Ninia, and Chersodromus. We also performed histological sections in seven individuals from the dipsadine genera Coniophanes, Hypsiglena, Imantodes, Leptodeira, and Urotheca (see Additional file 2). Histological sections were performed on previously fixed specimens housed in several scientific collections. Heads were skinned from the nostril to the neck and removed from the specimens at the level of the first cervical vertebra. Specimens and their head skin were thus returned to their jar in the collection. Heads from cientific collections were post-fixed with Bouin and submitted to decalcification and serial sections in the same way as live individuals (see below).
Additionally, live adult individuals of Dipsas neivai, D. indica, D. albifrons, Sibynomorphus mikanii, and S. neuwiedi were used in this work for more accurate histological procedures (see Additional file 2). Live specimens were provided by the Laboratório de Herpetologia do Instituto Butantan. They were euthanized through an intraperitoneal injection of sodium thiopental (30 mg/Kg). We removed either the complete head or only the infralabial glands of euthanized specimens for architectural analysis of the glands and associated duct systems and muscles. All specimens were preserved in formalin and deposited in the herpetological collections of the Instituto Butantan and Museu de Zoologia da Universidade de São Paulo.
The heads were fixed in Bouin fixative for 24 hours and posteriorly submitted to decalcification in 4.13% aqueous EDTA, pH 7.2, renewed every other three days, and kept in constant stirring for 60 days. The heads were then sagittally divided in two halves, dehydrated in ethanol, embedded in paraffin, and submitted to serial, sagittal or horizontal sectioning. Sections of 7 μm were obtained in a Microm HM 340 E microtome with disposable steel blades. All sections were submitted to hematoxylin-eosin (HE) staining for general study of the tissues, and to Mallory trichrome staining  for the specific identification of collagen and muscular fibres and epithelia.
Dissected glands were fixed during 24 hours in 4% paraformaldehyde in PBS 0.1 M, pH 7.2, dehydrated in ethanol and embedded in historesin (glycol methacrylate, Leica, Nussloch/Heidelberg, Baden-Württemberg, Germany). Sections of 2 μm were obtained in the same Microm HM 340 E microtome mounted with glass knives. Some sections were stained with toluidine blue-fuchsin  for a general view of the glandular condition. The remaining historesin sections were subjected to the following histochemical staining procedures : periodic acid-Schiff (PAS), alcian blue pH 2.5 and combined PAS and alcian blue pH 2.5 [61, 62] for the identification of neutral (PAS) and acid (alcian blue) mucosubstances, and bromophenol blue for the identification of proteins.
Photomicrographs were obtained with an Olympus BX51 microscope and an Olympus SZ stereomicroscope (Olympus, Tokyo, Japan) equipped with a digital camera and with the software Image-Pro Express (MediaCybernetics, Maryland, USA).
Availability of supporting data
The matrix is also deposited in the treeBase data repository (http://treebase.org/treebase-web/home.html), available through http://treebase.org/treebase-web/search/study/summary.html?id=15015.
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The authors are deeply indebted to Francisco L. Franco, Eliana Serapicos (Instituto Butantan), Robert Murphy, Ross McCullough (Royal Ontario Museum), Darrel Frost, David Kizirian (American Museum of Natural History), Ronaldo Fernandes, Ulisses Caramaschi, José Roberto Pombal Jr. (Museu Nacional da Universidade do Rio de Janeiro), William Duellman, Linda Trueb (Museum of Natural History, University of Kansas), W. Ronald Heyer, Jorge Zug, Roy McDiarmid, Kevin de Queiroz (National Museum of Natural History), Marco Altamirano Benavides, Mario Yánez-Muñoz (Museu Ecuatoriano de Ciencias Naturales), Douglas Rossman (Louisiana State University), Jim McGuire and Carol Spencer (Museum of Vertebrate Zoology, University of California, Berkeley) for providing important specimens for dissection. We are also grateful to Jeffrey A. Wilson and Marcelo R. de Carvalho for reviewing the manuscript. This research was carried out in strict accordance with Federal laws in Brazil. The protocol was approved by the Committee on the Ethics of Animal Experiments (Comitê de Ética em Pesquisa) of the Escola Paulista de Medicina, Universidade Federal de São Paulo (Permit Number: CEP 0277/05). This research was supported by grants from Fundação de Amparo à Pesquisa do Estado de São Paulo (BIOTA/FAPESP 2011/50206-9; http://www.biota.org.br/) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq 565046/2010-1, 303545/2010-0, 308950/2011-9, PROTAXA 562171/2010-0) to HZ and ALP. LO and MC are supported by a Ph.D. scholarship (number 2008/57102-1) and a Postdoctoral grant (number 2012/12587-3) from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP), respectively. The funders had no role in design, collection, analysis, and interpretation of data, in the writing of the manuscript, or in the decision to submit the manuscript for publication.
The authors declare that they have no competing interests.
HZ conceived the research. HZ, LO, ALP designed the research. HZ, LO, FGG, MC, CJ, MMA, ALP analyzed the data. HZ, LO, FGG, MC, CJ, MMA, ALP wrote the paper. HZ, LO, FGG, ALP prepared the figures. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 3: Tree estimated from a Maximum Likelihood analysis of 11 concatenated genes using RAxML 7.2.8. All outgroups are shown in the tree. Bootstrap values greater than 70% are given above each node. (PDF 190 KB)
Additional file 4: Fifty percent Majority-rule consensus tree estimated from a Bayesian analysis of 11 concatenated genes using MrBayes 3.1.2. All outgroups are shown in the tree. Bayesian Posterior Probability frequencies greater than 0.80 are given above each node. (PDF 169 KB)
Additional file 5: Dipsas albifrons on a snail of the genus Bradybaena, filmed in captivity at the biotherium of the Laboratório de Biologia Celular of the Instituto Butantan. Specimen was collected in Jaraguá do Sul, State of Santa Catarina, Brazil (body length = 525 mm; tail length = 183 mm). (WMV 8 MB)
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Zaher, H., de Oliveira, L., Grazziotin, F.G. et al. Consuming viscous prey: a novel protein-secreting delivery system in neotropical snail-eating snakes. BMC Evol Biol 14, 58 (2014). https://doi.org/10.1186/1471-2148-14-58