- Research article
- Open Access
Evolutionary and developmental considerations of the diet and gut morphology in ceratophryid tadpoles (Anura)
BMC Developmental Biology volume 20, Article number: 16 (2020)
Before metamorphosis, almost all anuran tadpoles are omnivores. Larval carnivory occurs in some species and, it is associated with distinctive morphotypes. Obligatory carnivorous tadpoles exhibit structural changes in the gastrointestinal tract compared to larvae that are predominately omnivores. The most distinctive feature of the anuran family Ceratophyridae (three genera) overall is the enormous gape of adults. This feature increases their ability to capture extremely large and active prey. The larvae of Ceratophyrid genera are remarkably distinct from each other and carnivory has diversified in a manner unseen in other anurans. The larvae of one genus, Lepidobatrachus, has a massive gape like the adult. Herein, we report on larval developmental variation, diet, gross morphology of the gastrointestinal tract, and histology of the cranial segment of the gut before, during and after metamorphosis in larval series for the following ceratophryid species: Chacophrys pierottii, Ceratophrys cranwelli, Lepidobatrachus laevis and Lepidobatrachus llanensis.
We described patterns of larval development with variation in growth with consequence to the final size at the end of metamorphosis. These patterns seem to be influenced by food quantity/quality, and most predominant by animal protein. Prey items found in pre and post-metamorphic Lepidobatrachus spp. are similar. Tadpoles of Ceratophrys and Chacophrys (and other anurans) share a short cranial segment of the gut with an internal glandular, mucous secreting epithelium, a double coiled intestine and the sequence of metamorphic changes (tract is empty, the stomach differentiates and the intestine shortens abruptly). In contrast, Lepidobatrachus tadpoles have a true stomach that acquires thickness and increased glandular complexity through development. As larvae they have a short intestine without double coils, and the absence of intestine shortening during metamorphosis.
The larval development of the gastrointestinal tract of Lepidobatrachus is unique compared with that of other free-living anuran larvae. An abrupt metamorphic transformation is missing and most of the adult structural features start to differentiate gradually at the beginning of larval stages.
Metamorphosis is a period of irreversible, dramatic ontogenetic change from a multicellular, free-living, post-embryonic stage (“larva” in animals) to a multicellular, pre-reproductive adult (“juvenile” in animals); it is also associated with a change in habitat . Before metamorphosis, almost all anuran larvae are omnivores. After metamorphosis, all anurans are carnivorous. Metamorphosis of the digestive system involves a transformation that includes the disappearance of the anal tube, extensive shortening of the alimentary tract, and differentiation of a stomach with the glandular complexity necessary to process a diet based on animal protein.
Larval carnivory occurs in some species and, where it is common, it is associated with distinctive morphotypes . Obligatory carnivorous tadpoles have a gastrointestinal tract that differs in structure from that of larvae that are predominately omnivores. Furthermore, a diet based on animal protein enhances development in carnivorous tadpoles [3, 4].
Frogs of the South American family Ceratophryidae (three genera: Chacophrys, Ceratophrys, Lepidobatrachus) are distinguished by robust bodies, short limbs, and massive heads, with an exaggerated mouth in which a pair of fangs protrude from the lower jaw. These features are associated with an evolutionary shift in the Ceratophryidae toward feeding on large prey, which includes many arthropod taxa, mollusks, anurans, snakes, lizards, birds and small mammals .
Tadpoles of ceratophryid genera are remarkably distinct, but they share accelerated developmental rates compared to tadpoles that are omnivorous and other taxa with obligated carnivorous tadpoles [6,7,8,9]. Carnivory has diversified in a manner unseen in other anurans since the Lepidobatrachus tadpole (with a massive gape) has become more like an adult .
Chacophrys has an omnivorous tadpole that feed on plankton and detritus. Its larval development occurs in just 2 weeks, with snout-vent length at the end of metamorphosis ranging from 20 to 45 mm (this article, ). Tadpoles of Ceratophrys are highly specialized carnivores with robust and sharp keratinized jaws. Larval development in Ceratophrys cranwelli takes 3 weeks, and snout-vent length varies between 30 and 40 mm at metamorphosis . Lepidobatrachus larvae are suctorial with a huge oral cavity. They swallow very large, living nekton including other tadpoles . After 2 weeks as larvae, newly metamorphosed Lepidobatrachus reaches snout-vent length between 40 and 50 mm [12, 13]. As previous authors have suggested, Lepidobatrachus has a life style in which larval and adult stages share a unique ecomorphology [9, 10]. Lepidobatrachus larvae have a short alimentary tract with a dilated cranial segment with a distinct glandular surface that is both structurally and functionally like the adult stomach. This includes a pepsinogen in early development that is electrophoretically indistinguishable from a form found in postmetamorphic Lepidobatrachus . Evolutionary novelties in Lepidobatrachus larvae include a capacious stomach, the greater ratio of foregut to hindgut than any omnivorous tadpoles, and a gastroduodenal loop in a more caudal position [15, 16].
Much is known about the morphology and ecology of the ceratophryids, in both larval and adult stages, but there is little comparative information on how modification of a common ancestral developmental pathway played a role in shaping their particular ontogenies. Here, from field specimens and field observations we provide data on 1) larval variation, 2) diet, 3) gross morphology, and 4) microscopic features of the anterior gastrointestinal before, during and after metamorphosis. Our results on ontogenetic variation in the gastrointestinal tract among ceratophryids provide insights to the evolution of the reduced ecomorphological differences between larvae and adults in Lepidobatrachus.
Intraspecific and interspecific developmental variation
Larval development for Chacophrys pierottii and Ceratophrys cranwelli (as representative species in the two genera) follows the sequence in the Gosner table . Stages 26–36 correspond to the proximo-distal differentiation of the hind limb followed by the postaxial-preaxial differentiation of autopodium. Stages 37–40 follow the appearance of tubercles in digits and limb growth. At Stage 41 the vent tube is lost. Stage 42 is diagnosed by forelimb emergence, loss of the larval denticles and horny beaks, and the cessation of larval growing. As most anurans, metamorphosis starts at this stage. Stages 43–46 are characterized by changes in the chondrocranium that convert the small-mouthed tadpole to a large-mouthed frog. During these stages, the tail shortens and finally disappears.
Lepidobatrachus spp. larvae lack digital tubercles and horny beaks. Their forelimbs develop externally. These features are so unusual that it is difficult to align Lepidobatrachus stages of limb growth and the beginning of the metamorphosis with standard Gosner stages. The major feature indicating metamorphosis in Lepidobatrachus is the degree of vent tube shortening and the formation of a cloaca. Other features that indicate the start of metamorphosis in the genus are the fusion of spiracle flaps with the forelimb skin and the disappearance of keratinized larval teeth.
Accelerated developmental rates in ceratophryid tadpoles described in previous studies (summarized in  and growth trajectories indicated they reach the metamorphosis at the minimum size of 30 mm of snout-vent (Fig. 1). However, there is a developmental series of Chacophrys pierottii with tadpoles metamorphosing at a smaller size (Fig. 1a). Small and large tadpoles belong to different clutches revealing an amplitude in size variation is greater to than reported previously .
Tadpole diets and gut contents through metamorphosis
Small tadpoles of Chacophrys pierottii graze on the pond bottom and their gut contents reveal principally detritus with pieces of dark organic fragments such as wood, shrimp eyes, insect pieces (Fig. 2a). Whereas large tadpoles feed actively in the water column and their gut contents show remnants of shrimp and algae (Fig. 2b, c). These tadpoles stop feeding when the forelimbs emerge and they shed their keratinized horny beaks (Stage 42). Gut contents diminish in a caudal direction and at Stage 44 the whole gastrointestinal tube is empty. When metamorphosis is complete, froglets (from large tadpole series) have empty guts (n = 5) whereas one contained eight Ch. pierottii tadpoles, and others (n = 2) insects (larvae and adult coleopterans). The cannibalism suggests emerging froglets forage at the margins of the pond.
Before metamorphosis, tadpoles of Ceratophrys cranwelli have an anterior stomach-like dilatation full of pieces of tadpoles (Fig. 2d), shrimp, and insects with the intestine filled with disassembled remnants of food. Tadpoles of C. cranwelli also stop feeding when their forelimbs emerge and they shed their keratinized beaks. Gut contents are reduced at Stage 43 and completely absent by Stage 44.
In contrast, for Lepidobatrachus laevis and L. llanensis tadpoles, ranging from larval limb bud stages to when their tails completely regressed (Stage 27–46) we always found prey items in their stomachs, which suggests that they do not stop feeding through metamorphosis. Prey items for both species included crustaceans, anurans, and insects (Table 1). L. laevis larval gut contents also included some snails.
The crustaceans Daphnia sp. and Hylallela sp. and anuran tadpoles were the dominant stomach contents in Lepidobatrachus larvae. These prey were predominant in the diet at all larval stages (Fig. 2e). At a similar stage and size, stomachs contents may present few and large prey (tadpoles) or much small prey (Hyallela sp.) suggesting there is no correlation between the size or stage of the tadpoles and the size of the prey that they had in their stomachs. The largest prey consumed are the crustacean Triops and tadpoles of various species (Table 1).
The stomach contents provide some indication of where Lepidobatrachus tadpoles feed. Tadpoles of Physalaemus biligonigerus, Rhinella major, and a metamorphosing Chacophrys pierottii (in the stomach of an advanced tadpole of L. llanensis) were likely captured near the edge of the pond where the water is shallow. Other prey are nektonic, consistent with the Lepidobatrachus tadpoles hunt in the water column.
We identified one case of cannibalism where a L. laevis eat a L. laevis tadpole and one case in which a L. laevis preyed upon on a Ceratophrys cranwelli tadpole. Ch. pierottii were found in the stomachs of L. llanensis. Small juvenile snails (Biomphalaria sp.) were present in the gut of L. laevis larvae at later stages.
Visceral gross morphology
Ceratophryid tadpoles share the following features of visceral gross morphology: 1) lungs are well developed and inflated early, at limb bud stages; 2) fat bodies are absent during larval development; and 3) gonads remain undifferentiated up to froglet stages.
In Chacophrys pierottii tadpoles (Stages 27–41), the coiled gut occupies almost the whole pleuroperitoneal cavity. It is visible through the skin in ventral view (Fig. 3a). In dorsal view, the liver and the pancreas are observed on the right side embraced by the gastroduodenal loop. This loop, which is in a relatively anterior position, is the most cephalic curvature of the gut: it delimits the esophagus and the cranial segment of the gut considered a larval “stomach” (i.e. the maniccotto glandulare, with a distinct internal glandular surface) from the intestine. The intestine is very long (Table 2), double spiralled, and arranged in a three-dimensional configuration of loops and coils. The intestine is uniform in diameter, its epithelium is corrugated and it is filled with organic matter.
Beginning with forelimb emergence, the gut proceeds to differentiate as follows: 1) the intestine is empty; 2) the diameter of the intestine diminishes posteriorly (from stage 42), 3) there is an abrupt shortening of the intestine (from stage 43) (Table 2); 4) the stomach differentiates (from stage 44), and 4) the rectum (different in diameter from the majority of the intestine) expands to form the ampulla.
The gastrointestinal tract in tadpoles of Ceratophrys cranwelli (Stages 26–41) presents a dilated stomach-like region, and a well-formed ampulla in the posterior intestine (Fig. 3b). The esophagus is a tube with longitudinal folds indicating a capacity to ingest a bolus of large diameter. The dilated foregut lies longitudinally, its wall is transparent with a glandular internal surface. The intestine is shorter than in Ch. pierottii (Table 2), double spiralled, and arranges in a three dimensional configuration of loops and coils. The ampulla of the hindgut is hemispheric and it is visible at left. Beginning with forelimb emergence the sequence of changes is as follows: 1) the intestine is emptying; 2) the diameter of the intestine diminishes; 3) the stomach differentiates, and 4) the intestine shortens (Table 2).
In Lepidobatrachus laevis and L. llanensis the stomach and the ampulla of the rectum occupy half of the pleuroperitoneal cavity as seen in the ventral view (Fig. 3c). The esophagus is a tube with longitudinal folds indicating it can expand to accommodate a large bolus of ingested material. The stomach is a dilated, long, transversally sac oriented with an internal glandular fundic area. The walls of the stomach increase thickness near the metamorphosis. The stomach continues as the duodenum separated by pyloric constriction. The intestine is shorter than in C. cranwelli (Table 2), it is arranged in a three-dimensional configuration of disorganized loops. The diameter of the intestine is uniform with irregular contents of digested organic matter. The ampulla of the rectum is oblong and it is visible anteriorly contiguous to the heart. These features are observed from early tadpoles up to postmetamorphic stages without changes in the intestine length (Table 2).
Microscopic morphology of the anterior segment of the gastrointestinal tract
In Chacophrys pierottii the larval esophagus shows a distended and thin mucosa, lined by a ciliated pseudostratified epithelium (Fig. 4a). Mucous secretory columnar cells positive for PAS staining are present in the epithelium indicating the secretion of neutral mucopolysaccharides. The submucosa layer is reduced, and the outer circular muscular layer is evident. In contrast, in postmetamorphic specimens, the epithelium forms a well-folded mucosa (Fig. 4b, c). In addition, small goblet cells concurrently stain positively for both PAS and AB confirming the presence of both acidic and neutral mucopolysaccharides. On the other hand, larger goblet cells are only positive for PAS, indicating the secretion of only neutral mucopolysaccharides (Fig. 4c). There are no tubular glands and the muscularis mucosa is sparse. The submucosa layer is wide and made up of loose connective tissue. External musculature is subdivided into a thick circular layer and a thin longitudinal layer.
The larval anterior stomach (manicotto glandulare) shows a fundic region. The mucosa is slightly folded and lined by a columnar epithelium with a brush border (Fig. 4d and e). Few goblet cells are observed; they stain purple with PAS. Tubular glands are observed, but they do not stain with either PAS or AB. The submucosa is not evident, and the outer circular muscular layer is present (Fig. 4e).
In postmetamorphic specimens there is an anterior region that transitions from an esophageal-like region to a fundic region. The middle portion of the stomach has almost entirely the histology of the fundic zone with a folded mucosa (Fig. 4f). The epithelium has secretory columnar cells with a brush border. Apical portion of the epithelial cells is reactive for both PAS and AB stains. There are tubular gastric glands that show mucous neck cells positive for PAS. Zymogen cells are observed mainly in the lower portion of the gastric glands. These cells have granules that stain differently with Masson’s trichrome or with light green (PAS/AB technique background dye) (Fig. 4g). The more caudal region of the stomach has pyloric features (Fig. 4h) with a homogeneous mucosa and shallow folds. The epithelium is made up of mucous secretory columnar cells that stain positively with PAS staining. Tubular glands are observed, but these are negative for combined PAS and AB staining. The layer muscularis externa is made up of a thick circular coat and a very thin longitudinal coat.
In Ceratophrys cranwelli the larval esophagus has a mucosa with numerous folds, lined by pseudostratified epithelium with ciliated columnar and goblet cells (Fig. 5a). Goblets cells stain bright purple with PAS. The submucosa layer is thin and is composed of loose connective tissue. The muscularis externa layer involves an inner circular coat and a very thin outer longitudinal coat (Fig. 5b). In contrast, in postmetamorphic specimens the submucosa and the muscularis externa layers are thicker.
The larval anterior stomach shows a fundic region with a distended mucosa (Fig. 5c). The epithelium has mucus secretory columnar cells with a brush border that is slightly PAS and AB positive. Very few PAS positive goblets cells are observed. Tubular gastric glands do not stain differentially with PAS or AB histochemical techniques. The submucosa layer is not evident but there is a thin muscular external layer (Fig. 5d).
In postmetamorphic specimens, the mucosa folds are pronounced and the stomach walls are thickened, including the submucosa and the muscularis externa layers. The cranial portion of the stomach progresses from an esophageal-like surface to a fundic surface similar to the middle stomach (Fig. 5e). The fundic surface has deep gastric pits (Fig. 5f). The epithelial lining is formed by brush-bordered columnar cells whose apical cytoplasm stains violet after combined PAS and AB staining. In addition, the mucosa has simple tubular gastric glands formed by mucous neck cells positive for PAS staining. The lower portion of gastric glands does not differentially stain with PAS/AB, but the cells show cytoplasmic granules with acidophilic characteristics. The muscularis mucosa layer is well defined. The submucosa is made up of loose connective tissue, and the muscularis externa involves an inner thick circular coat and outer longitudinal coat.
The caudal stomach has a distinct pyloric region. In larvae, the mucosa is slightly folded and is lined by a columnar epithelium. Few PAS-positive goblets cells are present (Fig. 5g). In postmetamorphic specimens, the pyloric region shows a slightly folded mucosa lined by an epithelium with mucous secretory columnar cells. In addition, there are small simple tubular gastric glands that do not differentially stain with PAS/AB or Masson’s trichrome (Fig. 5h). Both larvae and post metamorphic specimens have a thin submucosa made up of loose connective tissue. The muscularis externa layer is composed of an inner thick circular layer and an outer thin longitudinal layer (Fig. 5g and h).
In Lepidobatrachus spp. the esophagus appears the same in early tadpoles and postmetamorphic specimens. It has a mucosa with numerous folds lined by pseudostratified epithelium with ciliated columnar and goblets cells (Fig. 6a). The number of goblet cells and folds increases during development. The goblets cells appear bright purple after PAS staining. The submucosa layer is composed of loose connective tissue, and no glands are visible in this layer. The muscularis externa layer has circular inner and outer longitudinal fibers. In the cranial region of the stomach an esophageal-like zone and a fundic zone similar to the middle stomach was observed (Fig. 6b).
The middle stomach has a slightly folded mucosa in early tadpoles. At those stages, there is no distinct muscularis mucosa or submucosa (Fig. 6c). Folds are more complex and the gastric pits become deeper as development progresses (Fig. 6d). The mucosa is lined by a secretory columnar epithelium with a brush border. The apical plasma membrane and apical cytoplasm of the epithelial cells appear violet with PAS and AB combined staining indicating the presence of acidic and neutral mucopolysaccharides. In addition, the mucosa layer shows simple tubular gastric glands formed by mucous neck cells that stain bright purple with PAS. Zymogen cells are present mainly in the lower portion of the gastric glands, but they did not stain positively with either PAS or AB (Fig. 6c).
In more advanced developmental stages, the granules in the cytoplasm of zymogen cells stain positive with light green (PAS/AB technique background dye) or Masson’s trichrome, indicating strong acidophilic characteristics (Fig. 6d–f). In addition, a submucosa formed by loose connective tissue is evident. The muscularis externa layer is formed by an outer very thin longitudinal and an inner thick circular coat (Fig. 6d).
The caudal region of the stomach has a distinct pyloric region, with an extensively folded mucosa (Fig. 6g–h). The epithelium is simple and columnar, with mucous secretory cells positive for PAS staining. The submucosa layer is wide and made up of loose connective tissue. The muscularis externa layer is subdivided into a thick circular internal and a very thin longitudinal external layer. The number of folds and the thickness of the inner circular muscle layer increase considerably as the tadpole’s progress toward metamorphosis (Fig. 6h).
Intraspecific and interspecific developmental variation
Phenotypic plasticity occurs in a stressful environment (e.g. ones with high competition). For example, when tadpoles of species of the spadefoot toads (Spea bombifrons and S. multiplicata) develop together, they diverge in large carnivorous morphs and smaller omnivorous morphs . For these toads, both field and experimental data provide strong argument supporting the evolutionary consequences of phenotypic and developmental plasticity .
Ceratophryid’s development has diversified leading to three different larval phenotypes (based on in trophic morphology and behavior). These are represented by the three extant genera, which may co-occur within the same pond . Differences among the three phenotypes are based on feeding but are also evident in size, some developmental trajectories, and duration of the larval development.
Ceratophryid share rapid growth and the large size at metamorphosis. In the field, larval development is completed in 2 weeks for Chacophrys pierottii and Lepidobatrachus spp., and 3 weeks for Ceratophrys cranwelli [11, 12]. Larval development for most other anurans breeding simultaneously with ceratoprhyid species extends from 20 to 75 days, with smaller sizes at metamorphosis when development is completed in 20 days . Accelerated rates of growth have been reported in the African frog Pyxicephalus adspersus that metamorphoses at snout-vent length of 22.4 mm after just 17 days of development .
Pond desiccation, competition, food availability, and food quality are factors that can influence the length of the larval period and size at the metamorphosis. Growth trajectories for C. cranwelli and Lepidobatrachus spp. reveal intraspecific variation that is likely influenced by food quantity. Although we do not have data on developmental time to say whether the smaller tadpoles of Ch. pierottii develop faster; they would seem to be predominant detritivorous and benthic. This fact suggests further studies to test experimentally the hypothesis if variation of growth in Ch. pierottii would be related to locomotion in drying ponds, and/or food.
Metamorphosis occurs only when the limbs have grown in size and differentiated enough to make terrestrial locomotion possible. In tadpoles of Ch. pierottii and C. cranwelli, like most anurans, metamorphosis begins the moment the vent tube is lost and the forelimb emerge. In Lepidobatrachus, the early loss of the vent tube indicates that remaining metamorphoric changes may promptly follow. This is consistent with that vent tube disappearing as the first sign of metamorphosis when it is experimentally induced with exogenous thyroxine .
Then, the accelerated rates of growth among ceratophryid lineages resulted in large size at the metamorphosis and modified developmental trajectories (e.g., earlier anal tube disappearance) that permit the threshold for metamorphose to be reached in exceptional short time.
Tadpole diets and gut contents through metamorphosis
Tadpole’s diets vary in the relative amounts of protein, carbohydrate, and lipids. Tadpoles of some species may adjust their foraging behavior to better meet their nutritional needs. Nutritional variation, in turn, may influence the size at or time to metamorphosis . Apparently, among ceratophryids diet influences the size at the metamorphosis rather than time.
As was reported previously and noted above, tadpoles of Ceratophrys and Lepidobatrachus are predators on other anuran larvae and for Ceratophrys their diet is predominantly based on tadpoles . Crustaceans however are an important part of Lepidobatrachus spp. diet. Stomachs of Lepidobatrachus tadpoles may contain a few large prey items or many small prey items, and their stomach contents indicate they are opportunistic predators, often preying on a wide variety of invertebrate (crustaceans, insects, and mollusks), and anuran larvae. Cannibalism is frequent. The absence of fish among their gut contents —even when numerous species of fish co-exist  with ceratophryid tadpoles— would indicate they are not able to catch fish; e.g., their speed or mobility protects them Lepidobatrachus tadpole predation.
In spite of the voracious feeding behavior, megalophagy and cannibalism attributed to adult Ceratophryidae, they are most likely generalist, and opportunistic predators, capable of eating relatively large food items, but many other items are also found in their diet . The large size of ceratophryid tadpoles compared to most sympatric tadpoles could contribute to their propensity toward anurophagy during larval and froglet stages in Chacophrys.
Some neuroendocrine regulators (neuropeptid Y, corticotropine-realising factor, α melanocyte-stimulating hormone, corticosterone, and leptine) are associated with food intake, behaviors, and the cessation of feeding in different periods of larval development [23, 24]. Like most anurans, the cessation of feeding for Chacophrys and Ceratophrys tadpoles is a distinct metamorphic event evidenced by the empty gastrointestinal tract. Furthermore, the loss of their keratinized mouthparts at metamorphosis precludes ingestion of most items their larvae prey upon. There is one report though of Ceratophrys ornata continuing feeding during metamorphic climax based on observations of tadpoles maintained in aquarium and fed Tubifex worms, which may not require keratinized mouthparts for capture .
Lepidobatrachus tadpoles, however, are different. Our data on gut contents suggest they can capture prey during all larval stages, including those at metamorphic climax when the tail shortens and the mouth is remodelling. Indeed prey items found in pre and postmetamorphic Lepidobatrachus spp. are similar .
To summarize, all ceratophryid tadpoles can consume animal food. Tadpoles of Lepidobatrachus eat both large or small prey and what they ingest pre and post metamorphosis are similar. At the end of the larval period, food intake seem to continue without the usual interruption at metamorphosis.
Visceral gross morphology
In anurans, the extensive larval intestine is eventually remodeled during metamorphosis to become the shorter adult intestinal tract [26, 27]. The patterns observed in Chacophrys tadpoles is similar to those reported for most omnivore tadpoles. At the metamorphosis, the gastrointestinal tract is empty, the stomach differentiates and the intestine shortens abruptly.
Distinctive “carnivore” morph in Spea is characterized by large jaw muscles, notched mouthparts and a short gut . These features are also observed in Ceratophrys tadpoles . Furthermore, Ceratophrys tadpoles share with Chacophrys (and other anurans) the cranial segment of gut (manicotto glandulare), a double coiled intestine and the sequence of metamorphic changes in gross morphology (i.e., intestinal tract is empty, the stomach differentiates and the intestine shortens abruptly).
In contrast, Lepidobatrachus tadpoles have a true stomach and a short intestine without double coils. Their metamorphosis does not involve emptying, differentiation, or shortening of the alimentary tract. During larval development, the wall of gastrointestinal tract thickens and the internal surface gains glandular complexity. The absence of metamorphosis of the gastrointestinal tract is unique (or at least unknown) in other anurans with free-living tadpoles.
Pharmacolocological experiments that induced phenotypes, which mimicked the interspecific morphological variation, provide some insights into the evolution of carnivory in ceratophryid lineage . The domain of Pitx2 expression correlates with the position of the gastroduodenal loop, and this loop is positioned more posteriorly in Lepidobatrachus (a pattern that can be reproduced in Xenopus and Ceratophrys using an RA synthesis inhibitor). From these results, one may assume that decreased RA (retinoic acid) signaling occurred only in Lepidobatrachus lineage. Also, as Lepidobatrachus and Ceratophrys share several TH dependent traits, such as rapid development and precocious pepsinogen production, it is reasonable to presume that TH signaling increased in the ancestor to all ceratophryids .
Before the thyroid gland becomes functional, THs (from egg yolk), deiodinases, and TR play different role to produce spatiotemporal in the differentiation of tissues with different TH sensitiveness in early embryos [28,29,30]. Consistent with this perspective, the histomorphology of the thyroid gland during larval development in Lepidobatrachus indicates they present low secretion of endogenous TH . This TH could be complemented by TH precursors or TH derived from eggs and/or larval food producing different tissue responses, such as the early and gradual differentiation of the adult-like gastrointestinal tract.
Arguments based in a shift in TH signals at early developmental stages of Lepidobatrachus may explain the derived structural features of the gastrointestinal tract.
Microscopic morphology of the anterior segment of the gastrointestinal tract
Ceratophrys cranwelli and Chacophrys pierottii larvae show a fundic region, also known as “glandularae manicotto” that is typical of anuran larvae . This region has tubular glands of uniform characteristics, mainly of oxyntic cells, different from the oxynticopeptic cells present in postmetamorphic specimens . The anatomical transformation of the gastric area during metamorphosis is extensive and includes thickening of the submucosa and external musculature, deepening of the gastric folds, and an increase in the number and types of gastric glands.
In contrast, the stomach of Lepidobatrachus larvae at earlier stages has distinctive gastric glands, large gastric folds, and a well differentiated elastic stomach (with thicker submucosa layer and external musculature). Tubular gastric glands show mucous neck cells that secrete neutral mucopolysaccharides and homogeneous like-oxyntic cells. The presence of mucous neck cells in early tadpoles of Lepidobatrachus is a unique feature for anuran larvae. In C. cranwelli, Ch. pierottii (this study), C. ornata these cells differentiate at the end of metamorphosis .
During early Lepidobatrachus larval development, oxynticopeptic cells with cytoplasmic granules like those present in adult stages appear. However, there is no evidence of zymogen granules in early tadpoles, which could related to glandular maturity. Oxynticopeptic cells capable of synthesizing and secreting pepsins are already present in earlier larvae stages of Lepidobatrachus .
Tubular gastric glands present uniform features throughout of the larval intestine. These gastric glands are formed by oxyntic cells, different from the oxynticopeptic cells, which are capable of secreting HCl and pepsinogen in adults [33, 34]. Absence of secretion of HCl denotes anuran larvae lack of a true stomach .
Further, differences between oxyntic cells and oxynticopeptic cells were also identified with electron microcopy in Rana temporaria . Oxyntic cells showed small and dense cytoplasmic granules that could secrete HCl. The endocrine function of cells in the gastric region would seem to develop already in R. temporaria tadpoles acquiring a more active function via increment of the number of endocrine cells and the size of secretory granules in carnivorous adults [34,35,36]. In contrast, other authors generalized the absence of secretion of pepsinogen and/or HCl in anuran larvae [33, 35, 37].
In all postmetamorphic specimens studied so far there is certain regionalization in the tubular gastric glands, and it is common to find mucous cells in the duct, and the oxynticopeptic cells in the alveolar portion. Oxynticopeptic cells can be identified by the presence of acidophilic zymogen granules [38,39,40,41] as is the case for Chacophrys pierottii (froglets) and Lepidobatrachus spp. (larval and postmetamorphic stages). However, oxynticopeptic cells in C. cranwelli, which appear at the end of metamorphosis showed acidophilic characteristics, but few zymogenic granules. Zymogen granules were not observed in adult of Rana aurora .
In Lepidobatrachus tadpoles, the gastric features of the stomach, characteristic of postmetamophic anurans, are well-defined at early stages. In contrast, the glandular differentiation of stomach surface occurs at the end of metamorphosis or later in Chacophrys and Ceratophrys.
Figure 7 summarizes the major points of this research. The monophyly of the ceratophryids is well supported by both morphological and molecular data . Rapid larval development, with accelerated growth seems to related with a distinctive TH physiology in the lineage [15, 31, 44].
The extreme trophic morphologies among ceratophryids could had been influenced by many ecological cues (food availability, food quality, pond desiccation, competition). Carnivory in ceratophryid lineage had two major consequences: the carnivore tadpole of Ceratophrys and the adult-like carnivore tadpole of Lepidobatrachus in which the gastrointestinal metamorphosis disappeared and the only conserved signal of that metamorphosis is the larval vent tube.
It remains to be investigated how much diet and/or exogenous THs have disrupted the ceratophryid development to a direct development of the gastrointestinal tract in the life cycle of Lepidobatrachus.
The study did not involve experiments, but is a comparative approach, to the anuran metamorphosis in non-model species. The data proceeded from wild caught specimens deposited in herpetological collections and field observations. The study did not included living specimens. Histological sections, anatomical parts from dissections, and gut contents are preserved with similar catalogue numbers to those in the collection.
We studied larval and postmetamorphic specimens of Chacophrys pierottii (Vellard, 1948), Ceratophrys cranwelli Barrio, 1980, Lepidobatrachus laevis Budgett, 1899 and Lepidobatrachus llanensis Reig and Cei, 1963. All specimens were collected in ephemeral ponds in various locations in North Argentina in public lands along roads. Specimens were euthanized with overdose of aqueous solution of Tricaine methanesulfonate (MS222, 6 g/l) and fixed in 10% formalin or Bouin’s fixative in the field.
All procedures to collect and kill specimens in the field comply with the legal requirements of current laws in Argentina (approved research protocol PICT 510). Secretaría de Medio Ambiente y Desarrollo Sustentable, Gobierno de la Provincia de Salta, República Argentina, provided authorization to collect field specimens (collection licences N°199,886/2011 and 227–216,600/064/2016). All specimens were accessioned as lots and are deposited in the Herpetological Collection of IBIGEO (IBIGEO-A) as is listed:
32°15′08.33″S, 63°07′00.09″W: Chacophrys pierottii: IBIGEO-A 1029, 64 larval specimens (Gosner Stages 37–46) collected 28/01/2006; IBIGEO-A 987, 7 adult specimens collected 19/12/2004; IBIGEO-A 2231, 96 larval specimens (Gosner Stages 26–32). Lepidobatrachus llanensis: IBIGEO-A 1122, 13 larval specimens (limb growth and metamorphic stages) collected 28/01/2006; IBIGEO-A 2277, 17 larval specimens (digit differentiation stages) collected 20/01/2018; IBIGEO-A 2279, 19 larval specimens (limb growth stages) collected 26/01/2018
28°43′59.85″S, 63°25′56.53″W: Chacophrys pierottii: IBIGEO-A 2288, 48 larval specimens (Gosner Stages 37–46) and IBIGEO-A 2289 postmetamorphic individuals collected 30/01/2015
23°14′49.78″S, 63°21′18.11″W: Lepidobatrachus laevis: IBIGEO-A 1322, 57 larval specimens (limb growth stages) collected 08/12/2009. Lepidobatrachus llanensis: IBIGEO-A 1321, 23 larval specimens (limb growth stages) collected 08/12/2009.
23°16′19.41″S, 63°17′12.20″W: Lepidobatrachus laevis: IBIGEO-A 2286, 18 larval specimens (digit differentiation and limb growth stages) and 3 postmetamorphic specimens collected 09/02/2019; IBIGEO-A 2287, 22 larval specimens (limb growth and metamorphic stages) collected 17/02/2019. Ceratophrys cranwelli: IBIGEO-A 2282, 22 larval specimens (Gosner Stages 33–39) collected 17/02/2019.
23°13′28.23″S, 63°49′26.63″W: Lepidobatrachus laevis: IBIGEO-A 1613, 13 larval specimens (digit differentiation stages) collected 12/01/2016. Lepidobatrachus llanensis: IBIGEO-A 2275; 78 larval specimens (limb bud stages) collected 13/01/2010.
23°12′44.36″S, 63°34′00.13″W: Lepidobatrachus laevis: IBIGEO-A 2291, 23 larval specimens (digit differentiation and limb growth stages), IBIGEO-A 2274, 165 larval specimens (limb bud stages) collected 01/11/2000. Lepidobatrachus llanensis: IBIGEO-A 567, 19 larval specimens (digit differentiation and limb growth stages) collected 01/12/1998. Ceratophrys cranwelli: IBIGEO-A 2290, 13 larval specimens (digit differentiation and limb growth stages) collected 27/12/2007.
23°21′50.31″S, 63°6′57.32″W: Lepidobatrachus laevis: IBIGEO-A 2276, 15 larval specimens (digit differentiation and limb growth stages) collected 09/02/2019. Lepidobatrachus llanensis: IBIGEO-A 2281, 7 larval specimens (digit differentiation and limb growth stages) and 4 postmetamoprhic specimens collected 09/02/2019.
24°43′57.59″S, 64°11′49.46″W: Ceratophrys cranwelli: IBIGEO-A2283, 78 larval specimens (Gosner Stages 35–41) collected 11/11/1997
24°55′58.66″S, 63°39′51.50″W: Ceratophrys cranwelli: IBIGEO-A 1937, 75 larval specimens (Gosner Stages 37–43) collected 16/02/2018.
22°31′11.65″S, 63°45′59.55″W: Ceratophrys cranwelli: IBIGEO-A 21, 45 larval specimens (Gosner Stages 26–33) collected 05/12/1991.
Larval development was staged according to the standard table for anuran embryos and larvae  and studied specimens were at larval stages corresponding to the stages: limb bud [26,27,28,29,30], digit differentiation [31,32,33,34,35,36], limb growth [37,38,39,40,41] and tail shortening (42–46).
Data were obtained from several sources: 1) variation of external morphology during the ontogeny. The ontogeny was described by observing the complete series of development using a stereomicroscope. To document growth, measurements of snout-vent length and total length (snout-tail tip length) in larvae were made with dial calipers (0.02 mm). These measurements are given in millimeters; 2) dissection of larval specimens of Ceratophrys cranwelli (n = 10), Chacophrys pierottii (n = 12), Lepidobatrachus laevis (n = 48), and Lepidobatrachus llanensis (n = 29) to analyze gut contents. We counted and/or identified items in the stomachs or cranial segment of the intestine to the lowest taxonomic level possible, 3) descriptions of gross visceral morphology and changes in the gastrointestinal tract in dissected specimens, and 4) histological sections of selected specimens. Specimens at stages of digit differentiation, limb growth, advanced metamorphosis, or recently metamorphosed were selected. Descriptions, illustrations, and photographs were made with Nikon SMZ1000 stereo dissection microscope and a Nikon E200 microscope. Photomicrographs were obtained with digital camera adapted.
The cranial segment of the gut or stomachs were removed and processed according to the standard histological techniques. Stomach fragments were dehydrated in ascending ethanol series (50–100%), cleared in xylene, and embedded in paraffin. The tissue blocks were serially cross-sectioned at 5 μm with a semiautomatic microtome (Leica RM 2245). Serial slices were stained with the Masson’s trichrome method . Combined Alcian Blue (AB) and periodic acid Schiff (PAS) methods were employed for the demonstration of acidic glycoconjugates and neutral glycoconjugates, respectively .
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Heyland A, Hodin J, Reitzel AM. Hormone signaling in evolution and development: a non-model system approach. BioEssays. 2004;27:64–75.
Pfennig DW, Rice AM, Martin RA. Field and experimental evidence for competition’s role in phenotypic divergence. Evolution. 2007;61:257–71.
Newman R. Developmental plasticity of Scaphiopus couchii tadpoles in an unpredictable environment. Ecology. 1989;70:1775–87.
Pfennig DW. The adaptive significance of an environmentally-cued developmental switch in an anuran tadpole. Oecologia. 1990;85:101–7.
Schalk CM, Montaña CG, Klemish JL, Wild ER. On the diet of the frogs of the Ceratophryidae: synopsis and new contributions. S Am J Herpetol. 2014;9:90–105.
Ruibal RR, Thomas E. The obligate carnivorous larvae of the frog Lepidobatrachus laevis (Leptodactylidae). Copeia. 1988;2:591–604.
Vera Candioti MF. Morphology and feeding in tadpoles of Ceratophrys cranwelli (Anura: Leptodactylidae). Acta Zool Stockholm. 2005;86:1–11.
Vera Candioti MF. Anatomy of anuran tadpoles from lentic water bodies: systematic relevance and correlation with feeding habits. Zootaxa. 1600;2007:1–175.
Fabrezi MF, Quinzio SI, Goldberg J, Cruz JC, Chuliver Pereyra M, Wassersug RJ. Developmental changes and novelties in ceratophryid frogs. EvoDevo. 2016;7:5.
Fabrezi M, Quinzio SI, Goldberg J, Cruz JC, Chuliver Pereyra M, Wassersug RJ. Phenotypic variation through ontogeny: ceratophryid frogs as a model. eLS. 2019. https://0-doi-org.brum.beds.ac.uk/10.1002/9780470015902.a0028510.
Quinzio SI, Fabrezi M, Faivovich J. Redescription of the tadpole of Chacophrys pierottii (Vellard, 1948) (Anura: Ceratophryidae). S Am J Herpetol. 2006;1:202–9.
Fabrezi M, Quinzio SI. Morphological evolution in Ceratophyinae frogs (Anura, Neobatrachia): the effects of heterochronic changes during larval development and metamorphosis. Zool J Linnean Soc. 2018;54:752–80.
Fabrezi M. Heterochrony in growth and development in anurans from the Chaco of South America. Evol Biol. 2011;38:390–411.
Carroll EJ, Seneviratne AM, Ruibal R. Gastric pepsin in an anuran larva. Develop Growth Differ. 1991;33:499–507.
Bloom S, Ledon-Rettig C, Infante C, Everly A, Hanken J, Nascone-Yoder N. Developmental origins of a novel gut morphology in frogs. Evol Dev. 2013;15:213–23.
Womble M, Pickett M, Nascone-Yoder N. Frogs as integrative models for understanding digestive organ development and evolution. Semin Cell Dev Biol. 2016;51:92–105.
Gosner KL. A simplified table for staging anuran embryos and larvae with notes on identification. Herpetologica. 1960;16:183–90.
Levis NA, Pfennig DW. Plasticity-led evolution: a survey of developmental mechanisms and empirical tests. Evol Dev. 2020;22:71–87.
Haas A. Larval and metamorphic skeletal development in the fast-developing frog Pyxicephalus adspersus (Anura, Ranidae). Zoomorphology. 1999;119:23–35.
Fabrezi M, Lozano VL, Cruz JC. Differences in responsiveness and sensitivity to exogenous disruptors of the thyroid gland in three anuran species. J Exp Zool B. 2019;332:279–93.
Kupferberg S. The role of larval diet in anuran metamorphosis. Am Zool. 1997;37:146–59.
Monasterio de Gonzo G. Peces de los Ríos Bermejo, Juramento y cuencas endorreicas de la Provincia de Salta. 1st ed. Museo de Ciencias Naturales y Consejo de Investigación Universidad Nacional de Salta; 2003.
Crespi EJ, Unkufer MK. Development of food intake controls: neuroendocrine and environmental regulation of food intake during early life. Horm Behav. 2014;66:74–85.
Bender MC, Hu C, Pelletier C, Denver RJ. To eat or not to eat: ontogeny of hypothalamic feeding controls and a role for leptin in modulating life-history transition in amphibian tadpoles. Proc Biol Sci. 2018;28:285(1875).
Fry A, Kaltenbach JC. Histology and lectin-binding patterns in the digestive tract of the carnivorous larvae of the anuran, Ceratophrys ornata. J Morphol. 1999;241:19–32.
Nieuwkoop PD, Faber J. Normal table of Xenopus laevis (Daudin). Amsterdam: North Holland Publ. Co.; 1956.
Shi Y-B. Amphibian metamorphosis: from morphology to molecular biology. New York: Wiley; 2000.
Morvan Dubois G, Sebillot A, Kuiper GG, Verhoelst CH, Darras VM, Visser TJ, Demeneix BA. Deiodinase activity is present in Xenopus laevis during early embryogenesis. Endocrinology. 2006;147:4941–9.
Morvan-Dubois G, Demeneix BA, Sachs LM. Xenopus laevis as a model for studying thyroid hormone signalling: from development to metamorphosis. Mol Cell Endocrinol. 2008;93:71–9.
Duarte-Guterman P, Langlois VS, Pauli BD, Trudeau VL. Expression and T3 regulation of thyroid hormone-and sex steroid-related genes during Silurana (Xenopus) tropicalis early development. Gen Comp Endocr. 2010;166:428–35.
Fabrezi M, Cruz JC. Ontogeny of the thyroid glands during larval development of south American horned frogs (Anura, Ceratophryidae). Evol Biol. 2014;41:606–18.
Lambertini G. Il manicotto glandulare di Rana esculenta nei suoi aspetti strutturali e nelle sue evoluzioni metamorfiche durante lo sviluppo. Ric Morfol Roma. 1929;9:71–88.
Barrington EJW. The delayed development of the stomach in the frog (Rana temporaria) and the toad (Bufo bufo). Proc Zool Soc London. 1946;116:1–21.
Rovira J, Villaro AC, Bodegas ME, Valverde E, Sesma P. Structural study of the frog Rana temporaria larval stomach. Tissue Cell. 1993;25:695–707.
Griffiths I. The form and function of the fore-gut in anuran larvae (Amphibia, Salientia) with particular reference to the manicotto glandulare. Proc Zool Soc London. 1961;137:249–83.
Villaro AC, Rovira J, Bodegas ME, Burrell MA, Garcı́a-Ros D, Sesma P. Immunocytochemical and ultrastructural characterization of endocrine cells in the larval stomach of the frog Rana temporaria tadpoles: a comparison with adult specimens. Tissue Cell 2001;33:462–477.
Dodd MH, Dodd JM. The biology of metamorphosis. In: Lofts B, editor. Physiology of the Amphibia. New York: Academic Press; 1976. p. 467–599.
Norris JL. The normal histology of the esophageal and gastric mucosae of the frog, Rana pipiens. J Exp Zool. 1959;141:155–73.
Ruiz MC, Acosta A, Abad MJ, Michelangeli F. Nonparallel secretion of pepsinogen and acid by gastric oxyntopeptic cells of the toad (Bufo marinus). Am J Physiol-Gastr L. 1993;265:934–G941.
Rovira J, Villaro AC, Bodegas ME, Valverde E, Sesma P. Metamorphic changes in the stomach of the frog Rana temporaria tadpoles. Tissue Cell. 1995;27:13–22.
Machado-Santos C, Pelli-Martins AA, Abidu-Figueiredo M, de Brito-Gitirana L. Histochemical and immunohistochemical analysis of the stomach of Rhinella icterica (Anura, Bufonidae). J Histol. 2014. https://0-doi-org.brum.beds.ac.uk/10.1155/2014/872795.
Ferri D, Liquori GE, Natale L, Santarelli G, Scillitani G. Mucin histochemistry of the digestive tract of the red-legged frog Rana aurora aurora. Acta Histochem. 2001;103:225–37.
Faivovich J, Nicoli L, Blotto B, Pereyra M, Baldo D, Barrionuevo S, Fabrezi M, Wild E, Haddad C. Big, bad, and beautiful: phylogenetic relationships of the horned frogs (Anura: Ceratophryidae). S Am J Herpetol. 2014;9:207–27.
Buchholz DR, Hayes T. Variation in thyroid hormone action and tissue content underlies species differences in the timing of metamorphosis in desert frogs. Evol Dev. 2005;7:458–67.
Bancroft JD, Gamble M. Editors. Theory and practice of histologial techniques. 5th edition. Philadelphia, PA: Churchill Livinsgtone, Elsevier; 2002.
We are grateful to Richard Wassersug for some helpful suggestions and in improving the English in this manuscript.
MF and JCC are funded by Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). This work is supported by PIP-CONICET 2014/497 and PICT 2016/510 to MF. The funders had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
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Fabrezi, M., Cruz, J.C. Evolutionary and developmental considerations of the diet and gut morphology in ceratophryid tadpoles (Anura). BMC Dev Biol 20, 16 (2020). https://0-doi-org.brum.beds.ac.uk/10.1186/s12861-020-00221-5
- Horned frog