Integrative taxonomic reassessment of Odontophrynus populations in Argentina and phylogenetic relationships within Odontophrynidae (Anura)
- Published
- Accepted
- Received
- Academic Editor
- Joseph Gillespie
- Subject Areas
- Biodiversity, Evolutionary Studies, Taxonomy, Zoology
- Keywords
- Integrative taxonomy, Allozymes, Advertisement call, Species delimitation, Macrogenioglottus, Odontophrynus, Morphometry, 16S rRNA sequences, Proceratophrys
- Copyright
- © 2019 Martino et al.
- Licence
- This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
- Cite this article
- 2019. Integrative taxonomic reassessment of Odontophrynus populations in Argentina and phylogenetic relationships within Odontophrynidae (Anura) PeerJ 7:e6480 https://doi.org/10.7717/peerj.6480
Abstract
Amphibians are the most vulnerable vertebrates to biodiversity loss mediated by habitat destruction, climate change and diseases. Informed conservation management requires improving the taxonomy of anurans to assess reliably the species’ geographic range. The genus Odontophrynus that is geographically refined to Argentina, Bolivia, Brazil, Uruguay and Paraguay includes currently 12 nominal species with many populations of uncertain taxonomic assignment and subsequently unclear geographic ranges. In this study, we applied integrative taxonomic methods combining molecular (mitochondrial 16S gene), allozyme, morphological and bioacoustic data to delimit species of the genus Odontophrynus sampled from throughout Argentina where most species occur. The combined evidence demonstrates one case of cryptic diversity and another of overestimation of species richness. The populations referred to as O. americanus comprise at least three species. In contrast, O. achalensis and O. barrioi represent junior synonyms of the phenotypically plastic species O. occidentalis. We conclude that each of the four species occurring in Argentina inhabits medium to large areas. The Red List classification is currently “Least Concern”. We also propose a phylogenetic hypothesis for the genus and associated genera Macrogenioglottus and Proceratophrys (Odontophrynidae).
Introduction
Distribution pattern of Neotropical amphibian diversity is not well understood because of incomplete information on taxonomy and distribution (Vieites et al., 2009; Winter et al., 2016). Yet amphibians are of high conservation concern, with almost 43% the currently known species being globally threatened and another 25% data deficient (Stuart et al., 2004). Taxonomic uncertainty stems partially from the prevalence of the morphospecies concept in most original descriptions of amphibian species (Frost, 2018). Morphological characters alone often fail to differentiate among closely related species due to the conservatism in the morphological evolution of anurans (Elmer, Dávila & Lougheed, 2007; Vences et al., 2010; Kaefer et al., 2013; Rojas et al., 2018). Advertisement calls act as powerful tools of premating isolation and can reveal morphologically cryptic species in sympatry, but in allopatry distinct species may give almost identical calls (Schneider & Sinsch, 2007; Köhler et al., 2017; Vacher et al., 2017). Delimiting species solely based on genetic distances obtained by barcoding approaches may inflate real species numbers by overestimating the taxonomic importance of intraspecific genetic structuring (Sukumaran & Knowles, 2017). Therefore, species delimitation should attempt to unite several lines of evidence to provide robust taxonomic hypotheses (Dayrat, 2005; Padial & De La Riva, 2010; Rojas et al., 2018).
South American anurans provide several examples for morphologically highly conserved genera in which integrative taxonomy led to reliable species delimitation and subsequent conservation priorities (De Magalhães et al., 2018; Fouquet et al., 2018; Von May, Lehr & Rabosky, 2018). The semi fossorial toads of the genus Odontophrynus pose a similar challenge because all original species descriptions are solely based on morphology and often too ambiguous for a reliable species distinction (Duméril & Bibron, 1841; Berg, 1896; Cei, Ruiz & Beçak, 1982; Di Tada et al., 1984; Cei, 1985; Martino & Sinsch, 2002; Rosset et al., 2006, 2007; Rosset, 2008; Caramaschi & Napoli, 2012; Rocha et al., 2017). Extant populations are currently assigned to 12 species that are placed into three phenetic groups based on overall morphological similarities, except for O. salvatori that is possibly a misplaced Proceratophrys species (Caramaschi, 1996; Amaro, Pavan & Rodrigues, 2009; Caramaschi & Napoli, 2012; Frost, 2018). The O. americanus group includes five nominal species (O. americanus, O. cordobae, O. juquinha, O. lavillai and O. maisuma), the O. occidentalis group three nominal species (O. achalensis, O. barrioi and O. occidentalis), and the O. cultripes group again three nominal species (O. carvalhoi, O. cultripes and O. monachus). Odontophrynus toads inhabit a latitudinal range of 5°S–41°S east of the Andes covering an altitudinal range from sea level to montane valleys of about 2,200 m above sea level (Turazzini, Taglioretti & Gomez, 2016; Santos-Silva et al., 2017).
The reliability of taxonomic assignment of populations to the currently recognized species is hampered by the overall similarity of external morphology, and assumed geographic ranges bear a high degree of uncertainty. Therefore, the status in the IUCN Red List of Threatened Species and resulting conservation needs are at least debatable, with seven species considered as “Least Concern,” one as “Vulnerable” and five as “Data Deficient” (IUCN, 2018). The three disjunct areas inhabited by the tetraploid O. americanus may indicate the presence of cryptic species (Rosset et al., 2006). The Odontophrynus sp. of the Sierra de San Luis may or not be conspecific with O. achalensis described from the Sierras de Cordoba (Di Tada et al., 1984). Diploid O. americanus-like populations reported from the vicinity of the disjunct O. americanus ranges have been recently described as three distinct species, O. cordobae in Central Argentina (Martino & Sinsch, 2002), O. maisuma in coastal Uruguay and Brazil (Rosset, 2008) and O. juquinha in Minas Gerais, Brazil (Rocha et al., 2017). It remains controversial, if diploids of the O. americanus group derived from tetraploids or tetraploids several times independently from diploids (Beçak & Beçak, 1974; Beçak, 2014). With respect to these issues and the validity of the phenetic groups within Odontophrynus, the most recent molecular phylogeny of Odontophrynus is inconclusive being based on only three of the 12 nominal taxa (Dias et al., 2013). Earlier phylogenies proposed by Amaro, Pavan & Rodrigues (2009), Pyron & Wiens (2011) as well as the recent one by Feng et al. (2017) agree in that Odontophrynidae is monophyletic and that Macrogenioglottus and Odontophrynus are sister taxa.
Consequently, a reliable taxonomic and geographic delimitation of Odontophrynus species requires an integrative approach critically evaluating information available on genetic differentiation and phenotypic plasticity. In this study we adopt the consensus protocol for integrative taxonomy to delimit species (Padial et al., 2010). Geographically, we focus on Argentina where most currently recognized Odontophrynus species and several populations of still undetermined taxonomic status occur. The character complexes included in the re-assessment of taxa are quantitative morphometrics, advertisement call features, allozyme differentiation and partial mitochondrial 16S rRNA sequences, all providing meaningful taxonomic information. Data refer to 34 populations, among them those at the type localities for reference. Sites of sympatry (O. americanus/O. occidentalis, O. cordobae/O. occidentalis) are contrasted with those in narrow contact zones (O. americanus/O. cordobae, O. achalensis/O. occidentalis) and sites of allopatry. Additional data on the molecular Odontophrynus diversity in Brazil are used for a broader phylogenetic view on Odontophrynidae (Amaro, Pavan & Rodrigues, 2009; Dias et al., 2013; Lyra, Haddad & De Azeredo-Espin, 2017). Specifically, we test the following hypotheses: (1) Phenotypic plasticity within and among Odontophrynus taxa is associated with corresponding genetic differentiation; (2) The phenetic groups within Odontophrynus represent distinct phylogenetic lineages; (3) The current Red List classification does not reflect the risks upon each species.
Materials and Methods
Study area and field sampling
We identified and sampled 34 local populations of toads pertaining to the genus Odontophrynus in Argentina (Table S1). The type localities of the nominal taxa O. achalensis Di Tada et al., 1984 (Pampa de Achala, Cordoba province), O. barrioi Cei, Ruiz, and Beçak, 1982 (Aguadita springs, Sierra de Famatina, La Rioja province), O. cordobae Martino & Sinsch, 2002 (Villa General Belgrano, Cordoba province) and O. lavillai Cei, 1985 (Villa de la Punta, Santiago del Estero province) were sampled to obtain topotypical individuals for taxonomic comparison. Unfortunately, the exact type localities of the most wide-spread species O. americanus (Duméril & Bibron, 1841) and O. occidentalis (Berg, 1896) are unknown because the original descriptions only state that the holotype of O. americanus was “sent from Buenos Aires” and that the holotype of O. occidentalis was collected in “Arroyo Agrio” in the Neuquén province (Frost, 2018). According to Lescure et al. (2002), the type locality of O. americanus is probably “rives du Rio Negro, Patagonie” in the Río Negro province (Argentina; D’Orbigny, 1847) at the southernmost part of the current geographical range. Still, populations of tetraploid O. americanus were readily distinguished from those of the diploid taxa by erythrocyte size (Rosset et al., 2006; Grenat, Salas & Martino, 2009). Populations of uncertain taxonomic assignment were tentatively referred to as O. cf. achalensis (Locality: La Carolina, San Luis province) or O. cf. barrioi (Localities: Aguada de Molle, Huerta de Guachi, San Juan province; Table S1). Material and data collected at the study sites were: (1) blood smears for ploidy assessment; (2) adult specimens for morphometric measurements, (3) records of advertisement calls, (4) muscle and liver homogenates for allozyme analyses and (5) alcohol preserved tissue for phylogenetic analyses (partial sequences of the mitochondrial 16S rRNA gene). The carcasses of specimens studied were deposited in museum collections; Table S1. The Córdoba Environment Agency (A.C.A.S.E.), Environmental Secretary of Córdoba Government (A01-2013), authorized our study and issued research and collecting permits.
Morphological data
In a first step, presumed ploidy (diploid/tetraploid) was verified by measuring the erythrocyte size, which correlates with the DNA content. Smears of fresh blood were air-dried and light-microscopically examined at a magnification of 1,000 × using an OLYMPUS BX50 following the procedures described in Grenat, Salas & Martino (2009). Specimens were euthanized, tissues sampled and carcasses preserved in 4% formaldehyde. Use of vertebrate animals was approved by the Ethics Committee Comité de Ética de la Investigación (COEDI) of the Universidad Nacional de Rio Cuarto. (https://www.unrc.edu.ar/unrc/coedi/index.html). The investigation was conducted according to the state law “Protection and Conservation of Wild Fauna” (Argentina National Law N° 22.421) and the Ethical Committee of Investigation of the National University of Río Cuarto (N° 38/11). The external morphology of 256 specimens was described quantitatively by measuring 15 morphometric distances (to the nearest 0.1 mm; Martino & Sinsch, 2002): (1) Snout-vent length (SVL); (2) maximal head width (HW); (3) head length (HL); (4) snout-eye distance (SED); (5) internarinal distance (IND); (6) interocular distance (IOD); (7) eye-narinal distance (END); (8) rostronarinal distance (RND); (9) eye diameter (ED); (10) humerus length (HL); (11) length of 3rd finger (F3L); (12) femur length (FL); (13) tibia length (TL); (14) foot length (FOL); (15) length of 4th toe (T4L). All measurements were taken by the first author. Morphometric raw data are available in Dataset S1.
Each variable was standardized by subtracting the sample mean and dividing by the sample standard deviation. The matrix of standardized variables was subjected to a principal component analysis with a fixed number of three PCs extracted. By this means, we explored the morphometric variability independent of taxonomic assignment and reduced the information to statistically unrelated factors. PC1 represents size-related features, PC2 and PC3 shape-related ones. Separate PCAs were run on the taxa of the phenetic groups. Assignment of populations to a phenetic group was based on the advertisement call structure (O. americanus-group: simple pulsed calls; O. occidentalis-group: complex calls consisting of several pulse groups; Salas & Di Tada, 1994; Martino & Sinsch, 2002). The morphospace built by three PC-axes was used to evaluate partitioning among taxa. A discriminant analysis (Procedure: backward selection) with a priori taxon assignment was applied to quantify the partitioning of morphospace for each phenetic group. Removal of one or more morphometric variables is based on an F-to-remove test. If the least significant variable has an F-value less than 4.0, it will be removed from the model. We used the discriminant analyses to assess the magnitude of correct taxon classification for the individuals of each predefined group. Due to the partial sympatry among species of the O. occidentalis group we tested for clinal variation of PCs along latitudinal and altitudinal gradients by a multiple regression analysis (Procedure: backward selection at F = 4.0). Significance level was set to α = 0.05. All calculations were performed using the statistical package statgraphics centurion, version XVIII (Statpoint Inc., Warrenton, Virginia, USA).
Bioacoustic data
Advertisement calls given by 302 individuals (series of 11–116 calls per individual) were recorded in the field using a DAT recorder Sony TCD-100© with stereo microphone ECM-MS907 Sony© and tapes TDK DA-RGX 60© (Table 1). Ambient temperature (to the nearest 0.5 °C) was registered at the individual calling sites (usually shallow water near shore) immediately after recording. Short advertisement call series are available as Audio S1–S8. Whenever possible, specimens were collected to obtain tissue samples and for morphometric measurements. Oscillograms, sonograms and power spectra of the call series were prepared with the Medav Mosip 3000 Signal Processing System or the PC program Adobe Audition 1.0. Each call series was characterized by nine parameters which were measured in three calls per series (terminology and procedure according to Martino & Sinsch (2002) and Schneider & Sinsch (2007)): (1) call duration (ms); (2) number of pulse groups per call (N); (3) duration of pulse group (ms); (4) interval between pulse groups; (5) pulses per pulse group (N); (6) pulse duration (ms); (7) interpulse interval (ms); (8) pulse rate (pulses/s); (9) dominant frequency (Hz). Bioacoustic raw data are available in Dataset S2.
(A) Individuals of the O. americanus-group | |||||||
---|---|---|---|---|---|---|---|
Morphometric variables with N = 151 observations | PC1 | PC2 | PC3 | Call variables with N = 227 observations | PC1 | PC2 | PC3 |
Eigenwert: 9.71 Variance explained: 64.7% | Eigenwert: 0.97 Variance explained: 6.5% | Eigenwert: 0.90 Variance explained: 6.0% | Eigenwert: 2.70 Variance explained: 45.0% | Eigenwert: 1.48 Variance explained: 24.7% | Eigenwert: 0.94 Variance explained: 15.6% | ||
SVL | 0.289 | −0.129 | 0.025 | Call duration | 0.286 | 0.497 | 0.508 |
HW | 0.295 | −0.103 | 0.096 | Pulses per call | −0.351 | 0.138 | 0.738 |
HL | 0.227 | −0.182 | 0.348 | Pulse duration | 0.454 | 0.352 | −0.229 |
SED | 0.226 | −0.510 | −0.067 | Interpulse duration | 0.486 | −0.342 | 0.229 |
IND | 0.221 | 0.067 | −0.364 | Pulse rate | −0.589 | 0.060 | −0.147 |
IOD | 0.165 | −0.039 | 0.754 | Dominant frequency | 0.074 | −0.700 | 0.266 |
END | 0.258 | −0.047 | 0.106 | ||||
RND | 0.220 | −0.463 | −0.303 | ||||
ED | 0.246 | −0.269 | −0.150 | ||||
HL | 0.296 | 0.144 | −0.080 | ||||
FL | 0.278 | 0.216 | −0.056 | ||||
TL | 0.298 | 0.162 | 0.092 | ||||
FOL | 0.289 | 0.218 | −0.026 | ||||
F3L | 0.264 | 0.371 | −0.134 | ||||
T4L | 0.261 | 0.324 | −0.047 |
(B) Individuals of the O. occidentalis-group | |||||||
---|---|---|---|---|---|---|---|
Morphometric variables with N = 105 observations | PC1 | PC2 | PC3 | Call variables with N = 75 observations | PC1 | PC2 | PC3 |
Eigenwert: 10.53 Variance explained: 70.2% | Eigenwert: 0.79 Variance explained: 5.3% | Eigenwert: 0.69 Variance explained: 4.6% | Eigenwert: 3.41 Variance explained: 37.9% | Eigenwert: 1.99 Variance explained: 22.1% | Eigenwert: 1.62 Variance explained: 18.0% | ||
SVL | 0.286 | −0.001 | 0.010 | Call duration | 0.397 | −0.079 | 0.429 |
HW | 0.291 | −0.009 | 0.020 | Pulse groups per call | 0.390 | −0.179 | 0.422 |
HL | 0.222 | −0.286 | 0.551 | Pulse group duration | −0.236 | 0.473 | 0.248 |
SED | 0.221 | −0.650 | −0.168 | Interpulse group interval | 0.059 | 0.612 | 0.134 |
IND | 0.223 | 0.485 | −0.381 | Pulses per pulse group | −0.453 | 0.138 | 0.073 |
IOD | 0.196 | 0.016 | 0.326 | Pulse duration | −0.231 | −0.117 | 0.600 |
END | 0.255 | −0.093 | 0.012 | Interpulse duration | 0.328 | 0.396 | −0.342 |
RND | 0.234 | −0.328 | −0.530 | Pulse rate | −0.365 | −0.384 | −0.194 |
ED | 0.247 | −0.057 | −0.270 | Dominant frequency | 0.362 | −0.160 | −0.196 |
HL | 0.288 | 0.075 | −0.036 | ||||
FL | 0.272 | 0.237 | 0.099 | ||||
TL | 0.289 | 0.045 | 0.166 | ||||
FOL | 0.284 | 0.052 | 0.121 | ||||
F3L | 0.270 | 0.236 | −0.033 | ||||
T4L | 0.270 | 0.135 | 0.094 |
Note:
For details see text.
The arithmetic means of these call parameters were calculated for each series (=individual) and used for further analyses. Thus, the basic data set describing the advertisement calls of the populations studied consisted of 10 variables (nine call parameters and the corresponding ambient temperature) with N = 302 observations. As several call variables co-vary with ambient temperature, we calculated linear regression models of call parameter vs. temperature and used the standardized residuals to obtain a temperature-adjusted data set for further analysis. Analogous to the treatment of morphometric data, a principal component analysis was run on call data subsets of populations with homologous call structure (simple calls with six variables vs. complex calls with nine variables) to explore the bioacoustic differentiation among the taxa of each phenetic group. The three PCs explaining most of the variance were extracted to describe the sound space utilized by Odontophrynus and its partitioning among taxa. Moreover, a discriminant analysis (procedure: backward selection at F = 4.0) was applied on standardized call variables to quantify the partitioning of among-taxon sound space. We used the discriminant analyses to assess the magnitude of correct taxon classification for the individuals of each predefined group. Due to the partial sympatry among species of the O. occidentalis group we tested for clinal variation of PCs along latitudinal and altitudinal gradients by a multiple regression analysis (Procedure: backward selection at F = 4.0).
Allozyme data
Liver samples were obtained from 147 individuals (Table S2). Samples were dissolved in one ml homogenate buffer (Tris–EDTA-NADP at pH 7.0) and stored at −65 °C until use. Aliquots of 0.3–3 μl liver homogenate were applied to commercial cellulose acetate plates (PHERO-cel, 5.7 × 14.0 cm) and submitted to a continuous horizontal electrophoresis (Hebert & Beaton, 1993). Buffer systems and duration of electrophoresis were 30–40 min at room temperature: (1) Tris–Glycine at pH 8.5 and constant 200 V; (2) Citric acid aminopropyl morpholine at pH 7.0 and constant 130 V. Following electrophoresis, each gel was stained using standard recipes (Murphy et al., 1996).
The allozyme pattern of liver tissue consisted of 10 enzyme systems controlled by a total of 14 putative loci: aspartate amino transferase (two loci, AAT, EC 2.6.1.1), carboxylesterase (1, EST, 3.1.1.1), glycerol-3-phosphate dehydrogenase (1, G3PD, 1.1.1.8), glucosephosphate isomerase (1, GPI, 5.3.1.9), isocitrate dehydrogenase (2, IDH, 1.1.1.42), lactate dehydrogenase (1, LDH, 1.1.1.27), malate dehydrogenase (2, MDH, 1.1.1.37), malic enzyme (1, ME, 1.1.1.40), 6-phosphogluconate dehydrogenase (1, 6PGD, 1.1.1.44), phosphoglucomutase (2, PGM, 2.7.5.1). Mitochondrial and cytoplasmatic loci were distinguished by prefixes (m/c), electromorphs (putative alleles) of each locus were designated alphabetically from cathode to anode. For reference, we used a sample of one O. americanus individual in each run.
Statistical analyses of data included the calculation of allele frequencies (Table S2) and Nei’s unbiased genetic distances (Nei, 1972). Distances >0.1 were considered indicative for differentiation at species level (Highton, 1999; Scillitani & Picariello, 2000). Calculation was performed using the program GENDIST of the Phylogeny Inference Package (PHYLIP, version 3.695) by Felsenstein (2008).
Molecular phylogenetic analysis
We compared the partial sequence of the mitochondrial 16S rRNA gene of the samples from the different localities in Argentina to assess the number of species present in the country and their phylogenetic relationships (Table S3). The 16S barcoding gene is widely used, it amplifies with great success for most amphibians, there is a lot of available information already, and it is generally informative for tree-tips relationships, that is, among closely related species (Vences et al., 2005; Zhang et al., 2013). DNA was extracted using Qiagen DNeasy Blood and Tissue Kit (Qiagen, Hilden, Germany) following the manufacturer’s protocol. Polymerase chain reaction (PCR) was used to amplify fragments of approximately 560 bp of 16S mitochondrial rRNA using the standard primers 16SAL (5′-CGCCTGTTTACTAAAAACAT-3′), and 16SBH (5′-CCGGTCTGAACTCAGATCACGT-3′). Amplification followed the standard PCR conditions (Palumbi, 1996) with the following thermal cycle profile: 120 s at 94 °C, followed by 33 cycles of 94 °C for 30 s, 49 °C (12S)/53 °C (16S) for 30 s, and extension at 65 °C for 60 s. All amplified PCR products were verified using electrophoresis on a 1.4% agarose gel stained with ethidium bromide. PCR products were purified using Highpure PCR Product Purification Kit (Roche Diagnostics, Risch-Rotkreuz, Switzerland). Sequencing of both strands was performed with the DYEnamic ET Terminator Cycle Sequencing Premixkit (GE Healthcare, Munich, Germany) for sequencing reactions run on a MegaBACE 1000 automated sequencer (GE Healthcare, Munich, Germany). Chromas lite 2.1.1 software (Technelysium Pty Ltd, South Brisbane, Australia; http://www.technelysium.com.au) was used to check and read the chromatograms of the sequences. The obtained sequences were compared with those in GenBank using a standard nucleotide-nucleotide BLAST search. Homologous sequences of Odontophynus as well as from species of the closely related genera Macrogenioglottus and Proceratophrys were downloaded from GenBank and incorporated in an alignment. Sequences of Pleurodema somuncurensis (Leptodactylidae), Rhinella marina (Bufonidae) and Ceratophrys cornuta (Ceratophrydae) were used as outgroups (Table S3) to represent related anuran families (Feng et al., 2017). The sequences were aligned using the MUSCLE algorithm (Edgar, 2004) implemented in MEGA 7 (Kumar, Stecher & Tamura, 2016). The final alignment consisted of 552 bp. Pairwise distances were calculated in MEGA7. Distances >1% were considered indicative for differentiation at species level (Sáez et al., 2014).
The general time-reversible model with proportion of invariable sites and gamma-distributed rate variation among sites (GTR + I + G) was chosen as the best-fitting model of sequence evolution on the basis of the Akaike information criterion as implemented in jModelTest 2 (Darriba et al., 2012) and was applied in maximum likelihood (ML) and Bayesian inference (BI) analyses. ML was performed in MEGA 7 with heuristic searches with stepwise addition and TBR branch-swapping algorithm, generating 1,000 bootstrap replicates. BI was performed using MrBayes 3.2.5 (Ronquist et al., 2012). Two independent Metropolis-coupled Monte Carlo Markov Chain (Larget & Simon, 1999) analyses were run for 10 Million generations, each with one hot and three cold chains and the temperature set at 0.2. Trees were sampled every 5,000 generations. The first 500 samples of each run were discarded as burn-in, and the remaining trees from both runs were used to calculate a consensus tree and Bayesian posterior probabilities.
Results
Morphological variation
All nominal taxa of Odontophrynus resemble each other considerably in coloration and external morphology reflecting their semi fossorial mode of living (Fig. 1). Quantitative morphometric analyses demonstrated a significant morphological variation among some taxa. The three principal component representing the axes of morphospace explained 77.2% of total variance in the O. americanus group and 80.1% in the O. occidentalis group, respectively (Table 1). The morphospace of the O. americanus group was partitioned between O. lavillai on one side and the indistinguishable pair O. americanus/O. cordobae on the other side (Fig. 2). The discriminant analysis confirmed a significant separation of O. lavillai with 85.7% of individuals correctly assigned to this species (Table 2). The taxa included in the O. occidentalis group showed a low morphometric differentiation with a wide overlap among O. occidentalis, O. achalensis and O. cf. achalensis (Fig. 3; Table 2). Classification success of discriminant function varied between 70% and 80% (Table 2). A significant proportion of morphometric variability among individuals assigned to the O. occidentalis group was caused by a clinal variation along altitudinal and latitudinal gradients. Size-related variation (PC1) was significantly correlated with altitude and latitude (Multiple regression model, R2 = 32.1%, F2,102 = 24.03, P < 0.00001), that is, size of individuals increased with elevation and from south to north. PC2 (position of nares and eyes) was significantly correlated with latitude (Multiple regression model, R2 = 16.6%, F1,103 = 20.52, P < 0.00001), PC3 (HL) with altitude (Multiple regression model, R2 = 10.0%, F1,103 = 11.42, P = 0.001).
Discriminant function | Eigenwert | Percentage | Canonical correlation | Wilks lambda | Chi-squared | Degrees of freedom | P-value |
---|---|---|---|---|---|---|---|
O. americanus-group | |||||||
1 | 1.91 | 95.7 | 0.810 | 0.316 | 168.7 | 8 | <0.00001 |
2 | 0.09 | 4.3 | 0.283 | 0.920 | 12.2 | 3 | 0.0067 |
O. occidentalis-group | |||||||
1 | 3.81 | 81.6 | 0.890 | 0.100 | 228.1 | 20 | <0.00001 |
2 | 0.44 | 9.5 | 0.554 | 0.480 | 72.6 | 12 | <0.00001 |
3 | 0.35 | 7.5 | 0.511 | 0.693 | 36.3 | 6 | <0.0001 |
4 | 0.07 | 1.4 | 0.249 | 0.938 | 6.3 | 2 | 0.0420 |
Standardized discriminant functions | ||||||
---|---|---|---|---|---|---|
O. americanus-group | O. occidentalis-group | |||||
Variables | 1 | 2 | 1 | 2 | 3 | 4 |
Maximum head width | 0.130 | 0.682 | −0.953 | −0.311 | ||
Snout-eye distance | −0.141 | 0.895 | 0.641 | 0.186 | ||
Tibia length | 0.692 | −1.11 | 0.454 | −1.028 | −0.441 | 0.427 |
Length of 3rd finger | 0.344 | 0.436 | 0.434 | 0.274 | 0.604 | 0.590 |
Length of 4th toe | 0.386 | −0.107 | 0.420 | −0.938 | ||
Eye-narinal distance | 0.370 | 0.333 | ||||
Rostronarinal distance | −0.268 | 1.051 |
Predicted species | |||||
---|---|---|---|---|---|
Actual species | O. americanus | O. cordobae | O. lavillai | ||
O. americanus (n = 66) | 63.6% (n = 42) | 36.4% (n = 24) | – | ||
O. cordobae (n = 57) | 38.6% (n = 22) | 57.9% (n = 33) | 3.5% (n = 2) | ||
O. lavillai (n = 28) | – | 14.3% (n = 4) | 85.7% (n = 24) |
Predicted species | |||||
---|---|---|---|---|---|
Actual species | O. occidentalis | O. achalensis | O. cf. achalensis | O. barrioi | O. cf. barrioi |
O. occidentalis (n = 29) | 75.9% (n = 22) | 3.5% (n = 1) | 10.3% (n = 3) | 6.9% (n = 2) | 3.5% (n = 1) |
O. achalensis (n = 20) | – | 80.0% (n = 16) | 20.0% (n = 4) | – | – |
O. cf. achalensis (n = 15) | 6.6% (n = 2) | 26.7% (n = 4) | 77.3% (n = 11) | – | – |
O. barrioi (n = 20) | – | – | 5.0% (n = 1) | 70.0% (n = 14) | 25.0% (n = 5) |
O. cf. barrioi (n = 21) | 9.5% (n = 2) | – | – | 19.1% (n = 4) | 71.4% (n = 15) |
Note:
Analyses were run separately on the two phenetic Odontophrynus groups. The subset include the smallest combination of measured variables that maximizes classification success. For details see text.
Advertisement call variation
The taxa of the O. americanus group emit simple and short pulsed advertisement calls, whereas those of the O. occidentalis group produce long and complex advertisement calls consisting of a variable number of short pulse groups (Fig. 4). Quantitative analyses of the advertisement calls based on six temperature-adjusted variables in the O. americanus group showed a significant variation among the three taxa. Three PCs explained 85.3% of total variance represented the axes of sound space (Table 1). The sound space was partitioned into three discrete groups representing O. americanus, O. cordobae and O. lavillai individuals, respectively (Fig. 2). The discriminant analysis assigned all but five calls correctly to the corresponding taxon (Table 3).
Discriminant function | Eigenwert | Percentage | Canonical correlation | Wilks lambda | Chi-squared | Degrees of freedom | P-value |
---|---|---|---|---|---|---|---|
O. americanus-group | |||||||
1 | 6.67 | 84.1 | 0.933 | 0.058 | 633.5 | 10 | <0.00001 |
2 | 1.26 | 25.9 | 0.747 | 0.443 | 181.1 | 4 | <0.00001 |
O. occidentalis-group | |||||||
1 | 12.25 | 90.3 | 0.962 | 0.028 | 245.5 | 24 | <0.00001 |
2 | 0.86 | 6.3 | 0.679 | 0.368 | 68.5 | 15 | <0.00001 |
3 | 0.44 | 3.2 | 0.552 | 0.683 | 26.2 | 8 | 0.0010 |
4 | 0.02 | 0.2 | 0.137 | 0.981 | 1.30 | 3 | 0.7296 |
Standardized discriminant functions | ||||||
---|---|---|---|---|---|---|
O. americanus-group | O. occidentalis-group | |||||
Variables | 1 | 2 | 1 | 2 | 3 | 4 |
Call duration | 0.877 | −0.429 | ||||
Pulse group duration | −0.636 | −2.144 | −0.107 | −1.092 | ||
Interpulse group intervall | −0.888 | −0.187 | −0.200 | 0.562 | ||
Pulses per pulse group | −0.423 | 0.202 | −0.503 | 1.450 | −0.419 | 0.442 |
Pulse duration | 0.275 | −0.406 | 1.205 | 0.744 | 0.353 | 1.315 |
Interpulse group intervall | 1.969 | 1.358 | 1.089 | 0.745 | ||
Pulse rate | −0.713 | −0.465 | ||||
Dominant frequency | 0.339 | 0.672 | 0.797 | −0.157 | −0.579 | 0.013 |
Predicted species | |||||
---|---|---|---|---|---|
Actual species | O. americanus | O. cordobae | O. lavillai | ||
O. americanus (n = 91) | 98.9% (n = 90) | – | 1.1% (n = 1) | ||
O. cordobae (n = 119) | 0.8% (n = 1) | 96.6% (n = 115) | 2.5% (n = 3) | ||
O. lavillai (n = 17) | – | – | 100% (n = 17) |
Predicted species | |||||
---|---|---|---|---|---|
Actual species | O. occidentalis | O. achalensis | O. cf. achalensis | O. barrioi | O. cf. barrioi |
O. occidentalis (n = 21) | 52.4% (n = 11) | 23.8% (n = 5) | 23.8% (n = 5) | – | – |
O. achalensis (n = 11) | – | 90.9% (n = 10) | 9.9% (n = 1) | – | – |
O. cf. achalensis (n = 10) | 40.0% (n = 4) | 20.0% (n = 2) | 40.0% (n = 4) | – | – |
O. barrioi (n = 11) | – | – | – | 100% (n = 11) | – |
O. cf. barrioi (n = 22) | – | – | – | 4.6% (n = 1) | 95.4% (n = 21) |
Note:
Analyses were run separately on the two phenetic Odontophrynus groups. The subset include the smallest combination of measured variables that maximizes classification success. For details see text.
Analogous to morphometric variation, sound space partitioning was low among the taxa of the O. occidentalis group, with O. occidentalis, O. achalensis and O. cf. achalensis being indistinguishable among each other (Fig. 3; Table 3). The sound space occupied by O. barrioi and O. cf. barrioi differed from the continuum formed by the other taxa, but showed a slight overlap between each other. Still, the correct classification rates for O. barrioi and O. cf. barrioi were 100% and 95.4%, respectively (Table 3). Temperature-adjusted advertisement call variation was also influenced by geographical clines. PC1 (size-related dominant frequency) and PC2 (call duration) were significantly correlated with latitude (Multiple regression models: R2 = 9.8%, F1,74 = 7.94, P = 0.0062, and R2 = 14.1%, F1,74 = 11.97, P = 0.0009, respectively), and PC3 (pulse group duration) with altitude (R2 = 9.1%, F1,74 = 7.31, P = 0.0085).
Genetic distances: allozymes and barcoding
A total of 14 putative loci were scored in the nominal taxa (Table S2). Two loci (mAAT, mMDH) were monomorphic in all taxa. The overall degree of allele fixation was high and varied between five loci in O. americanus and 11 in O. lavillai. Five taxa possessed one private allele each: O. americanus cIDH a, O. lavillai cAAT a, O. achalensis LDH d, O. cf. achalensis GPI d and O. barrioi cMDH a. The pairwise Nei distances among the taxa were clearly below species level in four taxon pairs (Table 4): 0.0220 in O. americanus/O. cordobae, 0.0232 in O. achalensis/O. occidentalis, 0.0292 in O. cf. achalensis/O. occidentalis, and 0.0351 in O. achalensis/O. cf. achalensis.
Taxon | O. cordobae | O. lavillai | O. occidentalis | O. achalensis | O. cf. achalensis | O. barrioi | O. cf. barrioi |
---|---|---|---|---|---|---|---|
O. americanus | 0.0220 | 0.1853 | 0.1821 | 0.1942 | 0.2452 | 0.4196 | 0.5471 |
O. cordobae | 0.2224 | 0.2084 | 0.2146 | 0.2707 | 0.4160 | 0.5943 | |
O. lavillai | 0.2781 | 0.4126 | 0.4982 | 0.6705 | 0.5608 | ||
O. occidentalis | 0.0232 | 0.0292 | 0.1846 | 0.2604 | |||
O. achalensis | 0.0351 | 0.1660 | 0.3422 | ||||
O. cf. achalensis | 0.1772 | 0.3406 | |||||
O. barrioi | 0.2186 |
Note:
Distances were calculated from the allele frequencies listed in S2.
The 25 samples from eight nominal Odontophrynus species differed from each other in the 16S sequences by uncorrected pairwise distances of 0.0–7.3% (Table 5). The divergence between samples of O. achalensis, O. barrioi, O. cf. barrioi and O. occidentalis were minimal (0.0–0.9%) and we regard them as belonging to a single species. The distances among the three nominal species O. americanus, O. cordobae and O. lavillai collected in Argentina were at species level (1.8–2.7%). Interestingly, the specimens referred to as O. americanus from Brazil (Amaro, Pavan & Rodrigues, 2009; Lyra, Haddad & De Azeredo-Espin, 2017) resolved into three groups differing at species level among each other (2.4–4.0%). The topotypic O. americanus from Argentina was conspecific with the Rio Grande specimen (southern Brazil; P-distance = 0.4 %). Genetic differentiation among the specimens collected in Argentina delimits four Odontophrynus species (Fig. 5).
Taxon | O. americanus (Minas Gerais, Brazil) | O. americanus (Sao Paulo, Santa Catarina, Brazil) | O. cordobae | O. lavillai | O. occidentalis | O. achalensis | O. barrioi | O. cf. barrioi | M. alipioi | P. bigibossa | C. cornuta |
---|---|---|---|---|---|---|---|---|---|---|---|
O. americanus (Buenos Aires, Argentina, Rio Grande, Brazil) | 2.4–3.5 | 2.4–4.0 | 2.1 | 2.5–2.7 | 4.6–5.2 | 4.6–5.0 | 5.2–5.6 | 5.0 | 5.9–6.2 | 8.7–9.3 | 10.8 |
O. americanus (Minas Gerais, Brazil) | 2.4–3.0 | 1.6–2.4 | 2.4–3.2 | 4.2–6.5 | 5.0–6.2 | 4.7–7.0 | 4.2–6.2 | 6.2–6.4 | 9.6 | 11.0 | |
O. americanus (Sao Paulo, Santa Catarina, Brazil) | 3.5–4.0 | 3.5–3.8 | 5.5–6.8 | 5.5–6.5 | 6.3–7.3 | 5.5–6.5 | 6.4–7.3 | 11.1–11.7 | 11.9–12.1 | ||
O. cordobae | 1.8 | 4.6–4.7 | 4.6 | 5.1 | 4.6 | 5.7–6.0 | 8.8 | 10.6 | |||
O. lavillai | 4.6–4.7 | 4.6 | 5.1 | 4.6 | 6.8–6.9 | 9.2 | 11.2 | ||||
O. occidentalis | 0.0–0.2 | 0.7–0.9 | 0.2 | 3.8–5.1 | 8.8–9.0 | 9.9–10.1 | |||||
O. achalensis | 0.7 | 0.0 | 3.8–4.9 | 8.8 | 9.9 | ||||||
O. barrioi | 0.7 | 3.8–5.3 | 8.6 | 9.7 | |||||||
O. cf. barrioi | 3.8–4.9 | 8.8 | 9.9 | ||||||||
M. alipioi | 8.8–9.0 | 9.5–10.6 | |||||||||
P. bigibossa | 11.0 |
Note:
Distances were calculated using the partial sequences of the mitochondrial 16S rRNA gene listed in S3.
Phylogenetic relationships among the Odontophrynidae
The topologies derived from the two phylogenetic analysis methods were largely congruent. We show the BI phylogeny with bootstrap values from ML and posterior probabilities from BI (Fig. 5). In agreement with earlier phylogenies (Amaro, Pavan & Rodrigues, 2009; Pyron & Wiens, 2011; Dias et al., 2013; Feng et al., 2017) our data support the monophyly of the three genera within Odontophrynidae and the sister group relationship between Macrogenioglottus and all Odontophrynus taxa. The Proceratophrys clade resolved as the sister group to the clade formed by the other two genera. The samples of Odontophrynus resolved into two major clades with strong node support. The first one contained the samples of O. occidentalis as well as those of O. achalensis and O. barrioi. The relationships within this clade remained largely unresolved and the three nominal taxa did not separate into distinct phylogenetic lineages. The second clade contained the remaining species divided into two subclades, one consisting of O. carvalhoi and O. cultripes, the other one containing O. americanus, O. cordobae and O. lavillai. The samples of O. americanus did not form a monophyletic clade since the topotypic Argentinian sample and the specimen from southern Brazil were more closely related to O. cordobae and O. lavillai than to the other Brazilian samples referred to as O. americanus.
Synonymy and updated diagnosis of O. occidentalis (Berg, 1896)
Since we did not detect significant genetic differentiation among O. achalensis, O. barrioi and O. occidentalis, we consider these three nominal taxa as a single species. Applying the Principle of Priority of the International Code of Zoological Nomenclature (International Commission on Zoological Nomenclature, ICZN, 1999), the oldest available name is O. occidentalis.
Synonymy. Besides the names C. occidentalis Berg, 1896 and O. occidentalis Müller, 1934, we place the names O. barrioi Cei, Ruiz, and Beçak, 1982, and O. achalensis Di Tada et al., 1984 into the synonymy of O. occidentalis (Berg, 1896).
Holotype. Male (MACN 380), housed in the Museo Argentino de Ciencias Naturales “Bernardino Rivadavia”, Buenos Aires, Argentina (Rosset et al., 2007). Type locality: “Arroyo Agrio (Neuquén)”, Argentina.
Molecular diagnosis. The partial mitochondrial 16S RNA gene sequences of 10 specimens collected throughout the geographical range (Table S3) are unique within the genus Odontophrynus, show a low within-taxon range of variation (0.0–0.9% uncorrected P-distances) and differ significantly from the corresponding sequences of O. americanus, O. cordobae and O. lavillai (4.6–5.2% uncorrected P-distances; Table 5) originating from Argentina.
Karyological diagnosis. The karyotype of O. occidentalis is diploid with 2n = 22 chromosomes as in O. cordobae and in O. lavillai, distinguishing these species from the tetraploid O. americanus (Barrio & Pistol de Rubel, 1972; Cei, Ruiz & Beçak, 1982; Ruiz, Cei & Beçak, 1982; Salas, Steinlein & Schmid, 2000; Rosset et al., 2006; Salas & Martino, 2007). Secondary constrictions are present on pair 4 in some O. americanus, all O. cordobae and O. lavillai and on pair 8 in O. cordobae and on pair 11 in O. americanus and O. occidentalis (Barrio & Pistol de Rubel, 1972; Rosset et al., 2006; Salas & Martino, 2007). The intercalary C-band on chromosome 9 is characteristic for all studied O. occidentalis populations, that is, present in the achalensis, barrioi and occidentalis ecotypes, but absent in the other Odontophrynus spp. (Ruiz, Cei & Beçak, 1982). C-banding patterns shows some variability among populations, with additional bands on chromosome 1 (barrioi), 2 and 3 (barrioi, occidentalis), and 4 (achalensis) (Ruiz, Cei & Beçak, 1982; Salas, Steinlein & Schmid, 2000). Odontophrynus occidentalis is diagnosed karyologically by the combination of 2n = 22 chromosomes, secondary constrictions on chromosome pair 11 and an intercalary C-band on chromosome 9.
Morphological diagnosis of adults. Odontophrynus occidentalis are short-legged and stout as all described Odontophrynus toads. Enlarged to rounded paratoid glands are present. Sexual size dimorphism absent. Individuals of lowland populations on average smaller than those of highland populations. In life, the dorsal color is brownish with brown spots and faint lateral and dorsal yellowish longitudinal bands, expression of light vertebral stripe variable from absent to short at the head or urostyle (Fig. 1). Ventral background color is whitish with scattered white granuli.
Further qualitative features are in wide agreement with the original descriptions in Berg (1896), Cei, Ruiz & Beçak (1982), Di Tada et al. (1984), Cei (1985) and Rosset et al. (2007). (1) Nostrils nearer to the snout than to the eyes, in lateral profile; (2) lateral fringes poorly or not developed on fingers; (3) metatarsal tubercle shovel-like, moderately developed; (4) short fore and hind limbs; (5) ED 1.7 times greater than eye-nostril distance; (6) interorbital distance longer than the upper eyelid width; (7) tibia slightly shorter than femur; (8) HL approximately one third of the SVL; (9) keratinous spines on the dorsum present mainly in highland populations. Among- and within-population variation exist in shape, size and number of the dorsal glands and in the presence and number of keratinous spines on the dorsum (Di Tada et al., 1984; Rosset et al., 2007).
Crespo & Cei (1983) proposed several morphometric ratios (tibiofibula length/fourth toe length, sacrum width/total length, sacrum width/vertebral column length, skull length/total length) to distinguish barrioi from occidentalis ecotypes. Rosset et al. (2007) rejected this proposal. Quantitative features (median, range in [mm]) of 92 males and 13 females are calculated irrespective of altitude and latitude at collection locality. (1) SVL: 54.1 (36.3–71.2, males) vs. 51.0 (42.0–71.2, females); (2) HW: 24.5 (15.4–29.6) vs. 24.4 (19.2–31.4); (3) HL: 18.3 (11.1–24.9) vs. 17.8 (13.1–23.4); (4) SED: 8.6 (5.1–10.9) vs. 8.1 (5.6–10.2); (5) IND: 4.0 (3.1–5.5) vs. 3.8 (2.7–5.6); (6) IOD: 3.6 (2.6–4.7) vs. 3.9 (2.8–5.1); (7) END: 4.5 (3.1–6.5) vs. 4.4 (2.8–6.1); (8) RND: 5.4 (3.3–6.7) vs. 5.0 (3.0–6.3); (9) ED: 7.5 (5.6–10.4) vs. 7.4 (5.5–9.8); (10) HL: 24.4 (15.9–33.4) vs. 24.4 (17.5–34.5); (11) F3L: 7.6 (5.9–11.6) vs. 8.1 (5.9–11.5); (12) FL: 22.3 (15.5–32.0) vs. 20.4 (15.1–29.8); (13) TL: 20.0 (13.4–26.8) vs. 19.8 (14.5–25.4); (14) FOL: 33.0 (22.4–45.1) vs. 31.5 (24.1–46.6); (15) T4L: 11.1 (6.9–16.7) vs. 10.6 (7.9–18.4).
Morphological diagnosis of tadpoles. In the exotrophic, lentic and benthic Odontophrynus spp. tadpoles, the body is ovoid in dorsal and ventral views and slightly depressed in lateral view, the snout is circular in dorsal and ventral views with an anteroventral oral disc, the eyes and nostrils placed dorsally, and the spiracle sinistral, short, and with an opening posterodorsally directed (Do Nascimento et al., 2013). Odontophrynus occidentalis differs from the other species by being considerably larger at stages 36–38 (average: 71.7 mm; maximum: 75 mm (Cei, 1987). Do Nascimento et al. (2013) and González et al. (2014) state that external tadpole morphology is very similar in the achalensis, barrioi and occidentalis ecotypes, unlike Cei & Crespo (1982). Shared characters apart from the general Odontophrynus spp. features are a tail, that is, larger than half of the total length with robust musculature and 2(2)/3(1) as labial tooth row formula. Among the distinguishing characters mentioned by Cei et al. (1982), Cei & Crespo (1982) and Cei (1987) for the barrioi ecotype, only the diverging form of the tip of tail (rounded contrary to acuminate in occidentalis and achalensis) has been confirmed by González et al. (2014). The significance of this difference remains unclear because phenotypic plasticity of tail morphology in response to syntopic predators is well-documented (Van Buskirk, 2009).
Bioacoustic diagnosis. Odontophrynus occidentalis is unique among all currently known Odontophrynus species by giving series of complex advertisement calls consisting of a variable number of pulse groups (Figs. 4B and 4C). Rosset et al. (2007) state that advertisement call features in the ecotypes achalensis, barrioi and occidentalis are very similar. The bioacoustic distinction of achalensis from occidentalis (Salas & Di Tada, 1994) and of barrioi from the other ecotypes (Rosset et al., 2007) is based mainly on differences in the dominant frequency (related to body size), in call duration (sensitive to environmental temperature), and in intercall interval (sensitive to behavioral interactions such as chorusing; Schneider & Sinsch, 2007). In fact, temperature-adjusted dominant frequency Standardized Dominant Frequency (SDF) was significantly correlated with SVL of the caller demonstrating that ecotype distinction reflects mainly size variation among populations (Linear regression model: SDF = 2.405–0.065*SVL, R2 = 0.623; F1,74 = 120.6, P < 0.0001; Fig. S1). SVL- and temperature-adjusted call duration did not differ significantly among the ecotypes (ANOVA, F4,74 = 2.14, P = 0.084).
The following features (median, range, n = 229) of O. occidentalis advertisement calls are calculated irrespective of the size of the calling individual and of ambient temperature, altitude and latitude at recording locality. (1) Call duration 2,619 ms (767–64,303 ms); (2) pulse groups per call 18 (5–348); (3) pulse group duration 98 ms (60–171 ms); (4) pulses per pulse group 7 (5–11); (5) interpulse group interval 57 ms (38–97 ms); (6) pulse duration eight ms (4–13 ms); (7) interpulse interval six ms (2–16 ms); (8) pulse rate: 48.3 pulses/s (24.9–65.3 pulses/s); and (9) dominant frequency 754 Hz (553–955 Hz). Features of the encounter call are given in Rosset et al. (2007).
Geographic and habitat range. Populations are present in a latitudinal range from 41°S in the Rio Negro Province to 27.5°S in the north of the Catamarca Province (Ruiz, Cei & Beçak, 1982; Rosset et al., 2007). The corresponding altitudinal range is from 690 m above sea level to 1,854 m in the Sierra Pie de Palo, 1,965 m in the Sierra de San Luis, 2,149 m in the Sierra de Achala, and 2,200 m in the Sierra de Famatina (Table S1). Terrestrial habitats include pastureland, montane grassland, shrubs, forests and rock outcrops. Aquatic habitats used for reproduction and larval development are exclusively creeks and slowly running rock pool sections of permanent streams.
Discussion
Lines of evidence obtained from phenotypic and genotypic character complexes in Odontophrynus toads exemplify the common dilemma of taxonomy—which level of character differentiation requires taxonomic consequences? Our case study demonstrates that phenotypic plasticity may result in an overestimation of species number (O. occidentalis group), whereas molecular data may reveal unexpected cryptic diversity in morphologically uniform populations (referred to as O. americanus). The following discussion of the three hypotheses basic to our investigation will present a revised view on the actual Odontophrynus species richness and propose a model of the phylogenetic relationships within the genus Odontophrynus.
Hypothesis 1: Phenotypic plasticity within and among Odontophrynus taxa is associated with corresponding genetic differentiation
Applying the consensus protocol for integrative taxonomy (Padial et al., 2010) we evaluate the support for the genetically delimited species O. americanus, O. cordobae, O. lavillai and O. occidentalis by the among-taxon variation of allozyme, morphology and bioacoustic character complexes. Congruence of genetic and phenotypic differentiation clearly delimits O. lavillai from the congeneric taxa in Argentina. Independent support for its distinction from the only sympatric Odontophrynus species stems from karyological features, that is, O. lavillai is diploid whereas topotypic O. americanus is tetraploid (Barrio & Pistol de Rubel, 1972; Cei, 1985; Rosset & Baldo, 2014). Natural hybrids between these species have not been detected.
The significant differentiation of 16S RNA gene sequence distinguishes between the tetraploid O. americanus and the diploid O. cordobae as does the advertisement call structure (Martino & Sinsch, 2002; this study). Congruent allozyme and morphometric differentiation seem to be absent (Barrio & Pistol de Rubel, 1972; this study). However, adjusting size by age reveals that the two species differ significantly in their ontogenetic growth trajectories (Martino & Sinsch, 2002) supporting the molecular distinction. Premating isolation mechanisms allow the two species to maintain reproductive isolation in the narrow zone of sympatry, as indicated by a very low incidence of triploid hybrids at only two localities (Grenat et al., 2018). Thus, cumulating available evidence on character differentiation (except for the allozyme pattern) supports the species status of these two taxa.
To our surprise, the 16S RNA gene sequence of a topotypical tetraploid O. americanus from the Buenos Aires province, Argentina and that of five specimens of unknown ploidy referred to as O. americanus from different localities in Brazil (Amaro, Pavan & Rodrigues, 2009; Lyra, Haddad & De Azeredo-Espin, 2017) differed so profoundly that we consider them as a complex of three distinct species. One sample from Rio Grande, Brazil proved to be very similar to the topotypical tetraploid O. americanus indicating that this species extends over Uruguay to southern Brazil. A second group of two specimens originating from southern Minas Gerais is termed here as O. aff. americanus 1 and a distinct species from topotypical tetraploid O. americanus. Its distinction from or similarity with the diploid O. juquinha from northern Minas Gerais remains to be studied in the future. Finally, a third group of three specimens from Sao Paulo and Santa Catarina provinces, termed here as O. aff. americanus 2, is a distinct species from Minas Gerais taxon and true O. americanus. One of these specimens originated from Irai which is about 100 km distant from the “O. americanus”-populations reported from the province Misiones, Argentina (Rosset et al., 2006). It seems reasonable to assume that the geographical range of O. aff. americanus 2 extends to Argentina in the west, but further studies are needed to resolve the relationship to the Misiones populations.
In contrast, we did not detect any significant genetic differentiation among the specimens belonging to different nominal taxa of the O. occidentalis group despite a considerable phenotypic plasticity among and within populations. Broadly overlapping variation in all character complexes surveyed demonstrates that O. achalensis from the Sierra de Cordoba and associated populations from the Sierra de San Luis are phenotypically and genetically indistinguishable from O. occidentalis. Sympatry of the two forms in the Sierra de Cordoba suggests ongoing gene flux between lowland and highland phenotypes. The taxonomic conclusion is straightforward—O. achalensis does not deserve species status; it is simply the highland ecotype of the eastern and central part of the O. occidentalis range. Applying the Principle of Priority of the International Code of Zoological Nomenclature (International Commission on Zoological Nomenclature, ICZN, 1999), we consider O. achalensis a junior synonym of O. occidentalis.
The case of O. barrioi is more complicated because the absence of significant genetic differentiation from O. occidentalis contrasts with considerable morphometric, bioacoustic and allozyme differentiation. The O. barrioi populations vary morphometrically only by their greater size whereas shape variation is the same as in the O. occidentalis/O. achalensis continuum. Within-species altitudinal and latitudinal size variation is well known in anurans (Sinsch, Pelster & Ludwig, 2015), and SVL differences alone appear to be poor indicators of species distinction (Rakotoarison et al., 2012; Rojas et al., 2016). Advertisement call variation is mainly based on differences in dominant frequency, again an indicator of size of the calling individual (Fig. S1) and thus, of low taxonomic significance. The features of qualitative external morphology proposed by Rosset et al. (2007) to diagnose O. achalensis, O. barrioi and O. occidentalis represent the extremes of a continuum between lowland and highland ecotypes, and between eastern and northern variants of the same species. For the same reason González et al. (2014) failed to detect significant morphological differences among the tadpoles within the O. occidentalis group refuting the claim of Cei & Crespo (1982). Moreover, defensive behavior of adults is also indistinguishable (Borteiro et al., 2018). Thus, the phenotypic peculiarities of O. barrioi seem responses to local environmental conditions rather than indicating taxonomically relevant information. Applying the Principle of Priority of the International Code of Zoological Nomenclature (International Commission on Zoological Nomenclature, ICZN, 1999), we consider O. barrioi a junior synonym of O. occidentalis.
In conclusion, we verify hypothesis 1 for the species of the O. americanus group, but not for the nominal taxa of the O. occidentalis group. Conflicting evidence from phenotypic and genotypic variation in the taxa of the O. occidentalis group demonstrates that adaptation to altitude and geographic isolation from conspecific populations (allopatry) may result in phenotypes that were erroneously referred to as distinct species. Molecular evidence melts down the O. occidentalis group to single, polymorphic and highly adaptable species O. occidentalis.
Hypothesis 2: The phenetic groups within Odontophrynus represent distinct phylogenetic lineages
Our phylogram is formed by three clades within Odontophrynus representing the morphologically defined O. americanus, O. cultripes and O. occidentalis groups (Fig. 5). The basal splitting of lineages separates O. occidentalis, the only species with complex advertisement call consisting of several pulse groups, from the two lineages with simple pulsed calls. The ancestral character state of advertisement call structure in Odontophrynidae is most likely a simple pulsed call, as also present in the sister group Macrogenioglottus alipioi (Abravaya & Jackson, 1978) and in most Proceratophrys. The species occurring in Argentina and Bolivia, the diploids O. cordobae and O. lavillai, and the topotypical tetraploids O. americanus are closely related, but the sister species relationship between O. americanus and O. cordobae is well resolved possibly indicating an autopolyploid origin of these tetraploids.
In conclusion, we verify hypothesis 2 with respect to the genetic base of the phenetic groups. Our reconstruction of phylogenetic relationships among these groups suggests that O. occidentalis evolved from the ancestral stock before the diversification of the O. americanus and O. cultripes group occurred.
Hypothesis 3: The current Red List classification does not reflect the risks upon each species
The geographical distribution of O. occidentalis is larger than previously appreciated extending to north (barrioi ecotype) and to east (achalensis ecotype) (Fig. 6). Odontophrynus occidentalis is endemic to Argentina inhabiting many localities in eight provinces covering about 16% of the territory. This species is highly adaptable to a wide altitudinal range, and tolerant to local sympatry with O. americanus and O. cordobae. Thus, the Red List classification “Least Concern” seems justified, whereas the associated ecotypes “achalensis” and “barrioi” (“Vulnerable” and “Data Deficient”) do not deserve classifications apart. With respect to the species referred to as O. americanus our study suggests strongly that there is more than one species involved. The nominal species O. americanus is certainly widespread in Argentina (16 provinces and ca. 67% of the territory) and extends to Bolivia and Paraguay in the north, and to Uruguay and southern Brazil in the east. The status “Least Concern” seems appropriate. The exact range of this taxon in Brazil remains to be assessed using barcoding for species identification. Most probably, the easternmost locality in Misiones pertains rather to O. aff. americanus 2 of Brazil than to the nominal taxon of Argentina. If this assumption proves true, the still undescribed Odontophrynus taxon would constitute the fifth species of this genus in Argentina. O. cordobae has the smallest area of distribution of the four species, occurs exclusively in the central part of the Cordoba province, and thus, is endemic to Argentina (Fig. 6). Recent assessment of localities inhabited demonstrates that there is a viable network of probably connected populations (Grenat et al., 2018). Therefore, we propose the classification “Least Concern” as long as there is no further shrinkage of its geographical range. Finally, O. lavillai inhabits eight provinces of Argentina as does O. occidentalis, but its range extends further north to Bolivia and Paraguay (Rosset & Baldo, 2014). The classification “Least Concern” seems reasonable for this species as well. The Red List status of newly described species from Brazil and Uruguay and those of the O. cultripes group are outside the scope of this study.
In conclusion, we falsify hypothesis 3 with respect to genetically delimited Odontophrynus species of Argentina.
Conclusions
Integrative taxonomy has proved to be the appropriate tool to cope with distinct levels of character differentiation in the morphologically highly conserved genus of Odontophrynus toads. Genotypic variation among the nominal taxa of the O. occidentalis group did not correspond to the phenotypic plasticity in response to altitudinal and latitudinal gradients found in the ecotypes “achalensis”, “barrioi” and “occidentalis”. Consequently, molecular evidence melts down the O. occidentalis group to a single, polymorphic species O. occidentalis. Whereas the number of species was grossly overestimated in this case, considerable genetic divergence between O. americanus originating from a topotypical population (Argentina) and specimens of unknown ploidy from Brazil indicates that specimens referred to as O. americanus in Argentina and in Brazil are distinct species except for the southernmost populations in Brazil. Phylogenetic relationships among Odontophrynus species suggest that O. occidentalis evolved from the ancestral stock before the diversification of the O. americanus and O. cultripes group occurred. Reliable taxonomic delimitation of Odontophrynus taxa allows for a precise assessment of the corresponding geographical ranges and for an informed basis of the Red List classification. The four species occurring in Argentina do not seem endangered currently, but the small geographic range of O. cordobae may require a future reassessment of the species’ status.
Supplemental Information
List of Odontophrynus taxa collected from 34 localities in Argentina.
All specimens were examined for morphometric analyses. Tissue samples used for allozyme and barcoding sequences were obtained from some of these individuals (see S2 and S3). At all localities we recorded advertisement calls of as many individuals possible, but only some were collected and preserved. Abbreviations for institutions are: Fundación Miguel Lillo, Instituto de Herpetología, Tucumán, Argentina (FML), zoological collection of the National University of Rio Cuarto (ECOALMUNRC) in Rio Cuarto, Argentina, Instituto y Museo de Ciencias Naturales (IMCNSJ), San Juan, Argentina, and the Zoologisches Forschungsmuseum „Alexander König“ (ZFMK) in Bonn, Germany.
Allozyme allele frequencies in six nominal Odontophrynus taxa.
Allozymes were scored with cellulose acetate electrophoresis and subsequently stained. The number of individuals scored is given in brackets.
Samples of taxa used for molecular genetic analyses (partial sequences of the 16S rRNA gene), their geographic origins, voucher specimens, GenBank accession numbers, and original sources.
Voucher abbreviations are AF (Laboratório de Citogenética de Vertebrados, Instituto de Biociências, Universidade de São Paulo, Brazil), CFBH (collection Célio F.B. Haddad, Universidade Estadual Paulista, Rio Claro, São Paulo, Brazil), CNP (Centro Nacional Patagónico, Chubut, Argentina), DB (Diego Baldo, Universidad Nacional de Misiones, Argentina), ECOALMUNRC (Zoological collection, National University of Rio Cuarto, Argentina), FSFL (field number of Felipe Sá Fortes Leite, Pontifícia Universidade Católica de Minas Gerais, Brazil), JC (field number of José Cassimiro, Universidade de São Paulo, Brazil), BB (Boris Blotto field series), MLP (Museo de La Plata, La Plata, Argentina), MVZ (Museum of Vertebrate Zoology, Berkeley, USA), MZUSP (Museu de Zoologia, Universidade de São Paulo, Brazil), QCAZ (Museo de Zoología de la Pontificia Universidad Católica del Ecuador), ZFMK (Zoologisches Forschungsmuseum Koenig, Bonn, Germany), ZSM (Zoologische Staatssammlung München, Germany), ZUFRJ (Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Brazil).
Size-related variation of dominant frequency in the advertisement call of the O. occidentalis group.
Linear regression model of male SVL [mm] on dominant frequency [Hz]. For statistical details see text.
Advertisement call of topotypical Odontophrynus achalensis.
Call recorded at 21.3 °C water temperature.
Advertisement call of Odontophrynus cf. achalensis.
Call recorded at 16.8 °C water temperature.
Advertisement call of Odontophrynus americanus.
Call recorded at 19.5 °C water temperature.
Advertisement call of topotypical Odontophrynus barrioi.
Call recorded at 15.1 °C water temperature.
Advertisement call of Odontophrynus cf. barrioi.
Call recorded at 18.1 °C water temperature.
Advertisement call of topotypical Odontophrynus cordobae.
Call recorded at 19.7 °C water temperature.
Advertisement call of topotypical Odontophrynus lavillai.
Call recorded at 24.3 °C water temperature.
Advertisement call of Odontophrynus occidentalis.
Call recorded at 17.5 °C water temperature.