Skip to main content

Morphology of lentic and lotic tadpoles from Madagascar



The morphology of anuran larvae is suggested to differ between species with tadpoles living in standing (lentic) and running (lotic) waters. To explore which character combinations within the general tadpole morphospace are associated with these habitats, we studied categorical and metric larval data of 123 (one third of which from lotic environments) Madagascan anurans.


Using univariate and multivariate statistics, we found that certain combinations of fin height, body musculature and eye size prevail either in larvae from lentic or lotic environments.


Evidence for adaptation to lotic conditions in larvae of Madagascan anurans is presented. While lentic tadpoles typically show narrow to moderate oral discs, small to medium sized eyes, convex or moderately low fins and non-robust tail muscles, tadpoles from lotic environments typically show moderate to broad oral discs, medium to big sized eyes, low fins and a robust tail muscle.


Amphibians are unique among tetrapod vertebrates by their biphasic and complex life cycle. Most extant amphibians possess free living aquatic larval stages undergoing a drastic bauplan change, called metamorphosis [1, 2]. In the order Anuran, the larval stage is commonly referred to as tadpole. The formation of specialized larval organs for food collection such as the oral disc and the filter apparatus enable tadpoles a broad use of food sources [3] and facilitate the occupation of a variety of niches. It is assumed that this has favoured the extensive anuran radiation [4], with almost 7400 species known today, thus markedly exceeding the number of species in the two other amphibian orders (Gymnophiona, Urodela) with less specialized larvae [5, 6].

Most anurans deposit their eggs in ephemeral or perennial lentic waters [6, 7]. Their larvae have in tendency a globular body, median to high fins, a non-robust tail musculature, a relatively small number of labial tooth rows and a pointed tail end [6]. They are usually allocated to the pond type (here called ‘lentic’). Altig and McDiarmid suggested this type of larvae being close to the hypothetical ancestral larval bauplan [6, 8]. These prevailing morphological traits are frequently found in representatives of most existing phylogenetic lineages [7].

Apart from lentic environments, anuran larvae can use lotic environments for development. Lotic larvae show a much greater morphological diversity than lentic ones [2, 9]. Their morphological features include an enlarged oral disc, a high number of labial tooth rows, an increased number of oral papilla, a depressed body, a robust tail musculature and low fins [6, 10,11,12]. These characters were altered at different extent and in differing combinations [11,12,13,14], and they are interpreted as adaptations to lotic conditions such as the current velocity. This is of particular interest in anuran biology, since the evolutionary change of the larval bauplan is understood as a constraint on the one hand [15], but is highly adaptive on the other hand [2]. Moreover, it is noteworthy, that apparently only a small number of lotic larvae has evolved additional organs in connection with their lotic habitat, such as the ventral sucker in Atelopus or Amolops tadpoles [6].

In this paper, we study tadpoles from lentic and lotic environments to assess the extent to which morphological alteration of lotic larvae mark a possible response to environmental conditions, namely the water current. A similar study was conducted by Sherratt et al. [16]. The authors used a landmark approach. Landmarks are a precise tool to understand shifts in body shape and body proportions [17]. However, there are limitations when it comes to the analysis of particular morphological features. In anuran larvae, this includes the presence or absence of specialized organs that are known in lotic tadpoles. Likewise, the remarkable morphological variation of tadpoles’ oral structures cannot be assessed using landmarks. Hence, they may perhaps not fully catch the story of the evolution of the anuran larval bauplan to lotic environments in its complexity, why we here suggest a combination of a categorically coded characters and continuous measurements of larvae from lentic and lotic environments.

Madagascan anurans are a suitable ‘model’ group for a comparative study of lotic and lentic tadpoles. First, more than 350 species are known from this island in only five to six radiations (at family and subfamily levels) [5, 18], which provides a high number of candidate species for analysis while, at the same time, reducing the potential impact of phylogenetic constraints on trait evolution. Second, larvae of about one third of all Madagascan species have been described, which is a high number compared to other regions (authors’ unpubl. data). Third, Madagascar is characterized by an enormous landscape diversity [19], offering a wide range of larval habitats.

We expect that our approach will confirm the existence of a general morphospace in which body proportions of larvae can evolve in response to habitat conditions, as shown by Sherratt et al. [16]. We also hypothesize that characters of lotic tadpoles can rather be explained by shared adaptive evolution than by shared synapomorphies.


Patterns and univariate analysis

Oral disc – position and shape

As shown in Table 1, in lentic tadpoles an anteroventral oral disc position prevails with a normal or folded disc type and a moderate disc width. In lotic larvae, the oral disc position is commonly anteroventral or ventral, while the oral disc type and width are (similar to lentic tadpoles) normal or folded and moderate, respectively. Significant differences (employing a Fisher’s exact rxc-test) in lentic versus lotic tadpoles are found in oral disc position and oral disc width (Table 1). Noteworthy, broad oral discs do only occur in lentic larvae.

Table 1 Distribution of character states and results of the Fisher’s exact rxc-tests

Oral disc – horny structures and marginal papillae

Most lentic and lotic species have more than five labial tooth rows, one row of marginal papillae and a V- or U-shaped and arched ventral jaw sheath. The dorsal jaw sheath of most lentic species is arched, while most lotic larvae have specialised sheaths (Table 1). In the characters marginal papillae, ventral jaw sheath and dorsal jaw sheath, significant differences between lentic and lotic species are evident (Table 1). Moreover, specialised papillae only occur in lotic larvae and missing jaw sheath only in lentic larvae.


While commonly lentic and lotic tadpoles have dorsolateral positioned and medium-sized eyes, with a normal eye distance, a significant difference is the relation of eye sizes. Only a few lentic larvae possess big eyes, while most of them have small eyes. In lotic species, this relation is reversed (Table 1).

Body and tail

Lentic and lotic tadpoles commonly share a rounded tail tip, which is more than 1.5 times longer than the depressed body. Most lotic larvae have a robust tail musculature and low fins, while lentic ones usually develop moderately low fins and a tail musculature classified as not robust. These differences in tail muscles and fins are highly significant (Table 1).

Multivariate analysis

A Categorical Principal Component Analysis (CATPCA) reveals that Principal Component (PC) 1 (eigenvalue: 3.557) is exclusively explained by oral structures (Table 2). Species positively correlated with PC1 in 84% of all cases have few (0-1 row) or ‘specialised’, while 46% of those negatively correlated have two or more rows of papillae. The oral disc position of the positively loading species in 48% of all cases is terminal, while those negatively loading are characterized by ventral or anteroventral oral disc positions. Funnel-shaped oral discs are only found in taxa positively correlated with PC1. Finally, most of the species in the negative range of PC1 possess more than five tooth rows (88%), while the majority of the species in the positive range have no or up to five tooth rows (71%).

Table 2 CATPCA scores for 15 characters based on tadpoles of 123 anuran species

The CATPCA shows that regarding PC2 (eigenvalue: 2.946) tail muscle width and height, fin height, eye size and interorbital distance are the decisive parameters with factor loadings ≥│0.5│ (Table 2). PC2 strongly correlates with body and eye characters that show a highly significant difference between lentic and lotic larvae in the univariate analysis. Quantifications of dimensions are provided in the Additional file 1. Tadpoles positively (negatively) correlated with PC2 have in average IOD/BW of 0.64 (0.55), ED/BL 0.15 (0.11), TMW/BW 0.51 (0.37), TMH/BH 0.66 (0.54) and MTH/TMHM of 2.11 (2.71). That is, species positively correlated with PC2 develop bigger and more distant eyes, stronger tail muscles and lower fins than those negatively correlated with PC2.

For detailed data see Additional files 1, 2 and 3.

As visible in Fig. 1a, most tadpoles are grouped at values in the range of − 1 to + 1 of both dimensions. Mainly lotic tadpoles occupy the uppermost range of PC1. They are all members of the subgenus Chonomantis of the genus Mantidactylus and the (M. aerumnalis, M. albofrenatus, M. brevipalmatus, M. delormei, M. melanopleura, M. opiparis, M. zipperi). Congenerics outside this subgenus are scattered elsewhere (Fig. 1b). The only lentic taxa in the uppermost range of PC1 are Dyscophus insularis and Paradoxophyla palmata; they are clearly distinguished from Chonomantis spp. along PC2, however (Fig. 1a, b). A clear gradient along PC2 is obvious from lentic (e.g. genera Mantella, Scaphiophryne) to lotic taxa (e.g. Mantidactylus, Boophis). In-between, larvae from both environments largely overlap at the range − 1 to 0.5. A group of lotic larvae of the genus Boophis (B. albipunctatus, B. andohahela, B. ankaratra, B. luciae, B. mandraka, B. sambirano, B. schuboeae, B. vittatus) is characterized by the uppermost area of PC2 (Fig. 1b), while other members of the genus (both lentic and lotic) are scattered elsewhere. It is noteworthy that, among many lentic tadpoles, only that of Paradoxophyla tiarano remains in the lowermost range of PC2 (Fig. 1a, b).

Fig. 1
figure 1

Scatterplots of scores of PC1 and PC2, grouped by (A) aquatic habitat (B) genus

Phylogenetic effects

With the goal to consider ‘noise’ from underlying synapomorphies in our dataset, we compare the Euclidean distances of PCs and uncorrected p-distances of the 16S rRNA with a Mantel-test. According to this, there is markedly low phylogenetic signal (r2 = 0.036, p ≤ 0.0001). As the uncorrected p-distance does not account for evolutionary change at the long-term (e.g., reverse or consecutive mutations), we additionally compare the matrix of the best substitution model (GTR + G + I model, see Methods) with that of the Euclidean distances of PCs also using a Mantel-test. Again, this suggests that comparatively little phylogenetic signal occurs (r2 = 0.028, p ≤ 0.001).


Characters of lentic versus lotic life

Based on univariate comparisons, we find significant differences between lentic and lotic larvae of Madagascan anuran species for oral disc position, oral disc width, ventral and dorsal jaw sheaths, marginal papillae, eye size, tail muscle and fin shape. Especially, lentic tadpoles always exhibit a narrow to moderate oral disc, almost always small to medium sized eyes and mostly not robust to slightly robust tail muscles with high fins [6, 18, 20]. This is most obvious in Scaphiophryne tadpoles [21,22,23].

The CATPCA also clearly discriminates lentic and lotic tadpoles. An exception is the lotic larva of Paradoxophyla tiarano, grouping with the lentic clade. We consider this as a potential bias due to the incomplete data available for the multivariate analysis (cf. Additional file 2). In general and in line to the findings of the rxc-test, tail muscles and fin shape show high factor loadings along PC2 in the CATPCA. As a rule-of-thumb, species positively correlated with PC2 share a lotic habitat and are characterized by bigger eyes, more robust tail muscles and lower fins than the lentic ones which are negatively correlated with the same dimension.

The prevalence of big eyes in lotic tadpoles is difficult to interpret, so their potential functional significance remains to be studied. In contrast, robust tail muscles and low fins have been previously suggested to represent a response to lotic environments [6, 10]. The occurrence of robust tail muscles and low fins in tandem can be interpreted as an adaption to strong currents, because low fins decrease the drag effect and the musculature generates enough thrust to cope with the current [24, 25]. However, robust tail muscles and low fins can be found in lentic tadpoles, as well. They are then found to be associated with surface-feeding [7, 10].

Additional considerations

In the uppermost range of PC1 (CATPCA; Fig. 1b), all species of Chonomantis (subgenus of Mantidactylus [26]), and the species Dyscophus insularis and Paradoxophyla palmata aggregate. The first mentioned have a broad, funnel-shaped and terminally positioned oral disc without any labial tooth rows, combined with an arched dorsal jaw sheath and specialised papillae. These larvae are surface-feeders that exploit the neuston of slow-flowing to stagnant areas in streams, which is possible through a broad funnel-shaped and terminally positioned oral disc [7, 10, 18]. It is obvious that the funnel-shaped oral disc of Chonomantis is not an adaptation to lotic life, as similar characteristics occur in lentic larvae such as of the South American hylid (phyllomedusine) genus Phasmahyla [20]. Likewise, a terminal oral disc is known from surface-feeding tadpoles in lentic environments [7], so that rather this character is associated with feeding than with lentic vs. lotic environments. Moreover, the arched dorsal jaw sheath does not determinate these tadpoles’ aquatic habitat, as it is a common larval character of the entire subfamily Mantellinae [6, 27, 28], comprising both lentic and lotic species. The specialised papillae of Chonomantis tadpoles can also be explained by the particular way of feeding [6, 18]. Likewise, there is evidence that the enigmatic oral disc characteristics of Dyscophus insularis and Paradoxophyla palmata tadpoles (i.e. absence of marginal papillae, jaw sheaths and labial teeth [19]), are adaptations to microphagous filter-feeding behaviour [29, 30].

Since PC1 is mainly explained by oral structures, we propose that this pattern within PC dimensions does not discriminate lentic versus lotic tadpoles per se. Our results suggest that rather trophic niche specialization may explain this variation along PC1. Additionally, it is necessary to keep in mind that Chonomantis is a well-supported monophylum [26]. This study does not provide enough evidence to exclude possible phylogenetic reasons for these tadpoles grouping together along PC1. But in general, as suggested by the result of the Mantel-tests, phylogeny has a minor effect on the arrangement of species along the PCs.

Methodical considerations

Although with 123 of the more than 350 Madagascan anuran species the proportion of described tadpoles is comparatively high for this region, this list is by far not complete [31]. Even if one considers that there are taxa where free living larvae are missing, e.g. in members of the genus Gephyromantis [32, 33], many Madagascan tadpoles obviously remain undescribed, so that we still consider our results as preliminary. Apart from this, the different degrees of accuracy and completeness of the tadpole and habitat descriptions, as well as the ‘subjectivity’ of certain character definitions in Additional file 4 may lead to variation in data quality and a potential bias. This may also apply to the numerous measurements used for the CATPCA that were taken from illustrations of tadpoles (as indicated in Additional file 2).

Moreover, it cannot be ruled out that information obtained from freshly hatched or nearly metamorphosing larvae cause certain ‘noise’. To account for a higher stability within the morphospace, we therefore re-ran the CATPCA for a reduced dataset considering only the 48 species for which data in Gosner [34] stages 30-39 were available (Additional file 2). The results differ slightly in some components, but fins and tail muscles are still suggested to be the most decisive characters delimitating lentic vs. lotic tadpoles. Detailed results are provided in the Additional file 5 (Quantification of categories in Additional file 1).

We suggest that especially the consideration of non-metric characters, such as of the mouthpart, allows for a comprehensive insight of larval aspects related to eco-morphological adaptations. Taking the valuable landmark study by Sherratt et al. [16], only five of our characters would also be mirrored: body shape, relative length of tail to body, fins, tail tip and in parts eye position. Comparing this list to the rxc-test results, only the shape of the fins significantly discriminated between lentic and lotic tadpoles in Madagascan species. On the other hand, in the same test, eight out of 15 additional characters were significantly different between these two tadpole guilds.

In the CATPCA, two out of four landmark-relevant (body shape represented as BH/BW and fins represented as MTH/TMHM) but nine out of fifteen additional characters significantly loaded on the two PCs extracted by us. Hence, aspects of functional morphology, e.g. in the context of adaptation of anuran larvae to lentic or lotic environments, are perhaps best understood in a holistic approach, including landmark data and additional coded morphological characters.


We show that Madagascan anuran larvae from lentic and lotic environments differ in external morphology and that there is only a limited influence of phylogeny. Lotic tadpoles show moderate to broad oral discs, medium to big sized eyes, low fins and a robust tail muscle. Lentic tadpoles have narrow to moderate oral discs, small to medium sized eyes, convex or moderately low fins and non-robust tail muscles. We thus support the hypothetical existence of a general tadpole morphospace in which body proportions can evolve in response to habitat conditions. It remains to be shown if this patterns (1) still is applicable to the complete dataset of Madagascan tadpoles and (2) if it universally applicable to anuran larvae.


Google Scholar and Web of Science were searched for “tadpole” and “Madagascar”, revealing in 31 publications dealing with larval descriptions of 123 Madagascan anurans [18, 20,21,22,23, 27, 28, 32, 33, 35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57].

We examined larvae of 43 and 80 species collected in lentic or lotic conditions, respectively. Taxonomy follows Frost [58]; larval stages follow Gosner [34]. All raw data are provided in Additional file 2.

For the Fisher’s exact rxc-test [59], 15 character state conditions were (1) either adopted from published references mentioned in the Additional file 2 or (2) obtained from illustrations therein. We categorized information according to the definitions in Additional file 4: (1) oral disc position: anteroventral, terminal, ventral; (2) oral disc type: funnel-shaped, normal or folded, specialised; (3) oral disc width: broad, moderate, narrow; (4) labial tooth rows: < 5, 2/3, > 5, 0; (5) marginal papillae: 1 complete or incomplete row, ≥ 2 complete or incomplete rows, specialised, no papillae; (6) eye position: more lateral than dorsal, more dorsal than lateral, dorsolateral; (7) distance between eyes: broad, intermediate, narrow; (8) eye size: big, intermediate, small; (9) body shape: depressed, moderately depressed, normal or globular; (10) relative length of tail to body: < 0.99, 1-1.49, 1.5-1.99, ≥ 2; (11) tail muscle: not robust, slightly robust, robust; (12) fins: convex shaped - not low, moderately low, low; (13) tail tip: pointed, intermediate, rounded; (14) ventral jaw sheath: V or U arch, arch or V inverted, horizontal, specialised, missing; (15) dorsal jaw sheath: V or U inverted, horizontal, arch, specialised, missing.

Characters (1), (2), (4)-(6) and (13)-(15) were used as categorical variables in the CATPCA [60]. In addition, morphometric characters were examined (see Abbreviations) follow the definitions of Altig and McDiarmid [6]. Using these characters, seven ratios were computed (1) either using information from references listed in the Additional file 2, or (2) if data not provided, taken with PixelRuler (, accessed 22 March 2021) from illustrated tadpoles in the respective publications: IOD/BW; ED/BL; ODW/BW; TMW/BW; TMH/BH; BH/BW; MTH/TMHM. We considered variables with factor loadings ≥│0.5│as significantly contributing to the respective PC.

To explore the potential role of phylogenetic signal, we consulted GenBank (, accessed 22 March 2021) and extracted 16S rRNA sequences of 115 species (for the remaining, no data were available). We used MEGA-X 11 [61] (, accessed 22 March 2021) and the online “robust phylogenetic analysis for everyone” tool [62] (, accessed 22 March 2021) for the following steps: (1) combining data to a single *fas file (MEGA-X 11), (2) first alignment and cleaning of areas of bad alignments via BMGE and GBLOCKS [62], (3) final alignment and calculating of p-distance matrix (MEGA-X 11), (4) testing for the best substitution model (which is GTR + G + I) of corrected distances and calculating the configuration for the alternative distance matrix using ‘jmodeltest2’ [63, 64] (, accessed 9 July 2021), (5) calculating GTR + G + I model using provided configuration of ‘jmodeltest2’ and resulting alternative distance matrix using PAUP* [65] (, accessed 9 July 2021). Then we calculated the Euclidean distances between PC1 and PC2 of the CATPCA, and finally, employing the ‘vegan’ [66] package for R, a Mantel-test was performed on both matrices using Spearman-correlation with 9999 permutations.

Availability of data and materials

All data generated or analysed during this study are included in this published article and its additional file.



Body height


Body length


Block Mapping and Gathering with Entropy


Body width


Categorical Principal Components Analysis


Eye diameter


Interorbital distance


Maximum tail height


National Center for Biotechnology Information


Oral disc width


Principal component


Tail muscle height


Tail muscle height at mid-length of tail


Tail muscle width


  1. Slade NA, Wassersug RJ. On the evolution of complex life cycles. Evolution. 1975;29:568–71.

    PubMed  Article  Google Scholar 

  2. Wassersug R. The adaptive significance of the tadpole stage with comments on the maintenance of complex life cycles in anurans. Am Zool. 1975;15:405–17.

    Article  Google Scholar 

  3. Der VB. Buccopharynx und der Filterapparat der Anurenlarven - Morphologie, Ultrastruktur, Funktion, Leistung bei der Nahrungsaufnahme und ökologische Bedeutung. Mainz Naturwiss Arch. 1996;34:187–263.

    Google Scholar 

  4. Yoder JB, Clancey E, Des Roches S, Eastman JM, Gentry L, Godsoe W, et al. Ecological opportunity and the origin of adaptive radiations. J Evol Biol. 2010;23:1581–96.

    CAS  PubMed  Article  Google Scholar 

  5. AmphibiaWeb. Berkeley, CA. University of California; 2020. Accessed 5 July 2021.

  6. Altig R, McDiarmid RW. Body plan. Development and morphology. In: McDiarmid RW, Altig R, editors. Tadpoles. The biology of anuran larvae. Chicago: University of Chicago Press; 1999. p. 24–51.

    Google Scholar 

  7. Wells KD. The ecology and behavior of amphibians. Chicago: The University of Chicago Press; 2007.

    Book  Google Scholar 

  8. Altig R, McDiarmid RW. Descriptions and biological notes on three unusual mantellid tadpoles (Amphibia: Anura: Mantellidae) from southeastern Madagascar. Proc Biol Soc Wash. 2006;119:418–25.

    Article  Google Scholar 

  9. Orton GL. The bearing of larval evolution on some problems in frog classification. Syst Zool. 1957;6:79–86.

    Article  Google Scholar 

  10. Duellman WE, Trueb L. Biology of amphibians. New York: McGraw-Hill Co; 1986.

    Google Scholar 

  11. Lamotte M, Lescure J. Les têtards rhéophiles et hygropétriques de l’ancien et du nouveau monde. I. Ann Sci Nat Zool. 1989;10:111–22.

    Google Scholar 

  12. Lamotte M, Lescure J. Les têtards rhéophiles et hygropétriques de l’ancien et du nouveau monde. II. Ann Sci Nat Zool. 1989;10:125–44.

    Google Scholar 

  13. Channing A, Hillers A, Lötters S, Rödel MO, Schick S, Conradie W, et al. Taxonomy of the super-cryptic Hyperolius nasutus group of long reed frogs of Africa (Anura: Hyperoliidae), with descriptions of six new species. Zootaxa. 2013;3620:301–50.

    CAS  PubMed  Article  Google Scholar 

  14. Anstis M. Tadpoles and frogs of Australia. Second ed. London: New Holland Publishers Pty Ltd; 2017.

    Google Scholar 

  15. Hanken J. Larvae in amphibian development and evolution. In: Hall BK, Wake MH, editors. The origin and evolution of larval forms. San Diego: Academic; 1999. p. 61–108.

    Chapter  Google Scholar 

  16. Sherratt E, Anstis M, Keogh JS. Ecomorphological diversity of Australian tadpoles. Ecol Evol. 2018;8:12929–39.

    PubMed  PubMed Central  Article  Google Scholar 

  17. Ilić M, Jojić V, Stamenković G, Marković V, Simić V, Paunović M, et al. Geometric vs. traditional morphometric methods for exploring morphological variation of tadpoles at early developmental stages. Amphib-Reptil. 2019;40:499–509.

    Article  Google Scholar 

  18. Grosjean S, Strauß A, Glos J, Randrianiaina RD, Ohler A, Vences M. Morphological and ecological uniformity in the funnel-mouthed tadpoles of Malagasy litter frogs, subgenus Chonomantis. Zool J Linnean Soc. 2011;162:149–83.

    Article  Google Scholar 

  19. Lourenço WR, Goodman SM. Biogeography of Madagascar. Mémoires de la Société de Biogéographie. Paris: Mus national Hist Naturelle; 1996.

    Google Scholar 

  20. Dias dos Santos PH, Mongin-Aquino M, Candioti FV, Carvalho-e-Silva AM, Baêta D. Internal larval morphology of two species of shining leaf frogs (Anura: Phyllomedusidae: Phasmahyla). South Am J Herpetol. 2018;13:44–53.

    Article  Google Scholar 

  21. Grosjean S, Glos J, Teschke M, Glaw F, Vences M. Comparative larval morphology of Madagascan toadlets of the genus Scaphiophryne: phylogenetic and taxonomic inferences. Zool J Linnean Soc. 2007;151:555–76.

    Article  Google Scholar 

  22. Grosjean S, Vences M. The tadpole of the toadlet Scaphiophryne marmorata from Madagascar. Zootaxa. 1986;2009:67–8.

    Google Scholar 

  23. Mercurio V, Andreone F. The tadpoles of Scaphiophryne gottlebei (Microhylidae: Scaphiophryninae) and Mantella expectata (Mantellidae: Mantellinae) from Isalo massif, south-Central Madagascar. Alytes. 2006;23:81–95.

    Google Scholar 

  24. von Seckendorf HK, Wassersug RJ. Tadpole locomotion: axial movement and tail functions in a largely vertebraeless vertebrate. Am Zool. 2000;40:62–76.

    Google Scholar 

  25. Van Buskirk J, McCollum SA. Influence of tail shape on tadpole swimming performance. J Exp Biol. 2000;203:2149–58.

    PubMed  Article  Google Scholar 

  26. Vences M, Glaw F. Revision of the subgenus Chonomantis (Anura: Mantellidae: Mantidactylus) from Madagascar, with description of two new species. J Nat Hist. 2004;38:77–118.

    Article  Google Scholar 

  27. Jovanovic O, Glos J, Glaw F, Randrianiaina RD, Vences M. Comparative larval morphology in Madagascan frogs of the genus Mantella (Amphibia: Mantellidae). Zootaxa. 2009;2124:21–37.

    Article  Google Scholar 

  28. Blommers-Schlösser RM. Biosystematics of the Malagasy frogs. I. Mantellinae (Ranidae). Beaufortia. 1979;29:1–77.

    Google Scholar 

  29. Blommers-Schlösser RMA. Observation on the larval development of some Malagasy frogs, with notes on their ecology and biology (Anura: Dyscophinae, Scaphiophryninae and Cophylinae). Beaufortia. 1975;24:7–26.

    Google Scholar 

  30. Glos J, Erdmann G, Dausmann KH, Linsenmair KE. A comparative study of predator-induced social aggregation of tadpoles in two anuran species form Western Madagascar. Herpetol J. 2007;17:261–8.

    Google Scholar 

  31. Glaw F, Vences M. A field guide to the amphibians and reptiles of Madagascar. 3rd ed. Köln: Vences & Glaw; 2007.

    Google Scholar 

  32. Randrianiaina RD, Glaw F, Thomas M, Glos J, Raminosoa N, Vences M. Descriptions of the tadpoles of two species of Gephyromantis, with a discussion of the phylogenetic origin of direct development in mantellid frogs. Zootaxa. 2007;1401:53–61.

    Article  Google Scholar 

  33. Randrianiaina RD, Wollenberg KC, Hiobiarilanto TR, Strauß A, Glos J, Vences M. Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis. J Nat Hist. 2011;45:2871–900.

    Article  Google Scholar 

  34. Gosner KL. A simplified table for staging anuran embryos and larvae with notes on identification. Herpetologica. 1960;16:183–90.

    Google Scholar 

  35. Randrianiaina RD, Strauß A, Glos J, Vences M. Diversity of the strongly rheophilous tadpoles of Malagasy tree frogs, genus Boophis (Anura, Mantellidae), and identification of new candidate species via larval DNA sequence and morphology. ZooKeys. 2012;178:59–124.

    Article  Google Scholar 

  36. Blommers-Schlösser RM. Biosystematics of the Malagasy frogs II. The genus Boophis (Rhacophoridae). Contrib Zool. 1979;49:261–312.

    Google Scholar 

  37. Andreone F, Vences M, Guarino FM, Glaw F, Randrianirina JE. Natural history and larval morphology of Boophis occidentalis (Anura: Mantellidae: Boophinae) provide new insights into the phylogeny and adaptive radiation of endemic Malagasy frogs. J Zool. 2002;257:425–38.

    Article  Google Scholar 

  38. Andreone F, Rosa GM, Noël J, Crottini A, Vences M, Raxworthy CJ. Living within fallen palm leaves: the discovery of an unknown Blommersia (Mantellidae: Anura) reveals a new reproductive strategy in the amphibians of Madagascar. Naturwiss. 2010;97:525–43.

    CAS  PubMed  Article  Google Scholar 

  39. Andreone F, Aprea G, Odierna G, Vences M. A new narrow-mouthed frog of the genus Paradoxophyla (Microhylidae: Scaphiophryninae) from Masoala rainforest, northeastern Madagascar. Acta Herpetol. 2006;1:15–27.

    Google Scholar 

  40. Glos J, Linsenmair KE. Descriptions of the tadpoles of Aglyptodactylus laticeps and Aglyptodactylus securifer from western Madagascar, with notes on life history and ecology. J Herpetol. 2004;38:131–6.

    Article  Google Scholar 

  41. Glos J, Glaw F, Vences M. A new species of Scaphiophryne from western Madagascar. Copeia. 2005;2005:252–61.

    Article  Google Scholar 

  42. Linsenmair KE, Glos J. Description of the tadpoles of Boophis doulioti and B. xerophilus from Western Madagascar with notes on larval life history and breeding ecology. Amphib-Reptil. 2005;26:459–66.

    Article  Google Scholar 

  43. Thomas M, Raharivololoniaina L, Glaw F, Vences M, Vieites DR. Montane tadpoles in Madagascar: molecular identification and description of the larval stages of Mantidactylus elegans, Mantidactylus madecassus, and Boophis laurenti from the Andringitra massif. Copeia. 2005;2005:174–83.

    Article  Google Scholar 

  44. Grosjean S, Thomas M, Glaw F, Vences M. The tadpole of the Malagasy treefrog Boophis rufioculis: molecular identification and description. Spixiana. 2006;29:73–6.

    Google Scholar 

  45. Raharivololoniaina L, Grosjean S, Raminosoa NR, Glaw F, Vences M. Molecular identification, description, and phylogenetic implications of the tadpoles of 11 species of Malagasy treefrogs, genus Boophis. J Nat Hist. 2006;40:1449–80.

    Article  Google Scholar 

  46. Vejarano S, Thomas M, Glaw F, Vences M. Advertisement call and tadpole morphology of the clutch-guarding frog Mantidactylus argenteus from eastern Madagascar. Afr Zool. 2006;41:164–9.

    Article  Google Scholar 

  47. Vejarano S, Thomas M, Vences M. Comparative larval morphology in Madagascan frogs of the genus Guibemantis (Amphibia: Mantellidae). Zootaxa. 2006;1329:39–57.

    Article  Google Scholar 

  48. Knoll A, Köhler J, Glaw F, Teschke M, Vences M. Larval morphology in four species of Madagascan frogs of the subgenus Brygoomantis (Mantellidae: Mantidactylus). Zootaxa. 1616;2007:49–59.

    Google Scholar 

  49. Randrianiaina RD, Liliane R, Preuss C, Strauß A, Glaw F, Teschke M, et al. Descriptions of the tadpoles of seven species of Malagasy treefrogs, genus Boophis. Zootaxa. 2009;2021:23–41.

    Article  Google Scholar 

  50. Randrianiaina RD, Köhler J, Glos J, Vences M, Glaw F. Where to grow in the Tsingy? Limestone rock pools as breeding habitats of the relict frog Tsingymantis antitra from Madagascar and description of its tadpole. Salamandra. 2011;47:77–89.

    Google Scholar 

  51. Randrianiaina RD, Strauß A, Glos J, Glaw F, Vences M. Diversity, external morphology and reverse taxonomy in the specialized tadpoles of Malagasy river bank frogs of the subgenus Ochthomantis (genus Mantidactylus). Contrib Zool. 2011;80:17–65.

    Article  Google Scholar 

  52. Schmidt H, Strauß A, Reeve E, Letz A, Ludewig-Klingner AK, Neb D, et al. Descriptions of the remarkable tadpoles of three treefrog species, genus Boophis, from Madagascar. Herpetol Notes. 2008;1:49–57.

    Google Scholar 

  53. Schmidt H, Glaw F, Teschke M, Vences M. Description of tadpoles of five frog species in the subgenus Brygoomantis from Madagascar (Mantellidae: Mantidactylus). Zootaxa. 1988;2009:48–60.

    Google Scholar 

  54. Schmidt H, Glaw F, Teschke M, Vences M. The tadpole of the Madagascar bullfrog, Laliostoma labrosum. Zootaxa. 2009;2005:67–8.

    Article  Google Scholar 

  55. Hiobiarilanto TR, Randrianiaina RD, Glos J, Strauß A, Vences M. Description of ten tadpoles in the genus Boophis from Madagascar. Zootaxa. 2010;2694:1–25.

    Article  Google Scholar 

  56. Herilala Ndriantsoa S, Randrianiaina RD, Ramilijaona Ravoahangimalala O, Vences M, Glos J. Description of two tadpoles of Malagasy treefrogs, Spinomantis sp. aff. Peraccae and Spinomantis tavaratra. Zootaxa. 2012;3248:66–8.

    Article  Google Scholar 

  57. Griep S, Glos J. Description of tadpoles of the frogs Heterixalus tricolor, H. carbonei and H. luteostriatus (Anura: Hyperoliidae) from western Madagascar. Zootaxa. 2020;4767:332–44.

    Article  Google Scholar 

  58. Frost DR. Amphibian species of the world: an online reference. New York: American Museum of Natural History; 2021. Accessed 1 May 2021

    Google Scholar 

  59. Tools for Science. St. Joseph, MN. College of Saint Benedict, Saint John’s University; 2020. Accessed 7 July 2020.

  60. Meulman JJ, Heiser WJ. IBM SPSS categories 20. — IBM Corporation; 2011.

    Google Scholar 

  61. Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol. 2018;35:1547–9.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  62. Lemoine F, Correia D, Lefort V, Doppelt-Azeroual O, Mareuil F, Cohen-Boulakia S, et al. NGPhylogeny.Fr: new generation phylogenetic services for non-specialists. Nucleic Acids Res. 2019;47:W260–5.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  63. Darriba D, Taboada GL, Doallo R, Posada D. jModelTest 2: more models, new heuristics and parallel computing. Nat Methods. 2012;9:772.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  64. Guindon S, Gascuel O. A simple, fast and accurate method to estimate large phylogenies by maximum-likelihood. Syst Biol. 2003;52:696–704.

    PubMed  Article  Google Scholar 

  65. Cummings MP. PAUP* (phylogenetic analysis using parsimony (*and other methods)). Sunderland: Sinauer; 2014.

    Google Scholar 

  66. Oksanen J, Blanchet FG, Kindt R, Legendre P, Minchin PR, O’Hara RB, et al. Vegan: community ecology package. R package version 2.4-3; 2017. Accessed 17 Apr 2021

    Google Scholar 

Download references


Two anonymous reviewers made valuable comments on a previous version of this paper.


AS and JL were supported by grants from VolkswagenStiftung to AS (AZ96 838) and SL (AZ96 838-1). Open Access funding enabled and organized by Projekt DEAL.

Author information

Authors and Affiliations



MV, BV, JL and SL designed the study, BV and JL collected all data and JL performed the analyses with help of OE, MV, AS and SL. All authors contributed to the writing, led by JL and SL. All authors have read and approved the final manuscript.

Corresponding author

Correspondence to Stefan Lötters.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Quantification of categories.

Additional file 2.

Data matrix of raw data.

Additional file 3.

PC scores of examined species.

Additional file 4.

Definitions of variation of 15 characters, as coded in Additional file 2.

Additional file 5.

Results of analysis using species in Gosner stages 30-39.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Laudor, J., Schulze, A., Veith, M. et al. Morphology of lentic and lotic tadpoles from Madagascar. BMC Zool 6, 28 (2021).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


  • Adaptation
  • Anura
  • Larva
  • Environment
  • Evolution