Xenopus fraseri: Mr. Fraser, where did your frog come from?
Ben J. Evans
aff001; Marie-Theres Gansauge
aff002; Edward L. Stanley
aff003; Benjamin L. S. Furman
aff001; Caroline M. S. Cauret
aff001; Caleb Ofori-Boateng
aff005; Václav Gvoždík
aff006; Jeffrey W. Streicher
aff008; Eli Greenbaum
aff009; Richard C. Tinsley
aff010; Matthias Meyer
aff002; David C. Blackburn
Authors place of work:
Department of Biology, McMaster University, Hamilton, ON, Canada
aff001; Max Planck Institute for Evolutionary Anthropology, Deutscher Platz, Leipzig, Germany
aff002; Florida Museum of Natural History, University of Florida, Gainesville, FL, United States of America
aff003; Department of Zoology, Beaty Biodiversity Research Centre, University of British Columbia, Vancouver, British Columbia, Canada
aff004; Forestry Research Institute of Ghana, Kumasi, Ghana
aff005; Institute of Vertebrate Biology of the Czech Academy of Sciences, Czech Republic
aff006; Department of Zoology, National Museum, Prague, Czech Republic
aff007; Department of Life Sciences, The Natural History Museum, London, United Kingdom
aff008; Department of Biological Sciences, University of Texas at El Paso, El Paso, United States of America
aff009; School of Biological Sciences, University of Bristol, Bristol, United Kingdom
Published in the journal:
PLoS ONE 14(9)
A comprehensive, accurate, and revisable alpha taxonomy is crucial for biodiversity studies, but is challenging when data from reference specimens are difficult to collect or observe. However, recent technological advances can overcome some of these challenges. To illustrate this, we used modern approaches to tackle a centuries-old taxonomic enigma presented by Fraser’s Clawed Frog, Xenopus fraseri, including whether X. fraseri is different from other species, and if so, where it is situated geographically and phylogenetically. To facilitate these inferences, we used high-resolution techniques to examine morphological variation, and we generated and analyzed complete mitochondrial genome sequences from all Xenopus species, including >150-year-old type specimens. Our results demonstrate that X. fraseri is indeed distinct from other species, firmly place this species within a phylogenetic context, and identify its minimal geographic distribution in northern Ghana and northern Cameroon. These data also permit novel phylogenetic resolution into this intensively studied and biomedically important group. Xenopus fraseri was formerly thought to be a rainforest endemic placed alongside species in the amieti species group; in fact this species occurs in arid habitat on the borderlands of the Sahel, and is the smallest member of the muelleri species group. This study illustrates that the taxonomic enigma of Fraser’s frog was a combined consequence of sparse collection records, interspecies conservation and intraspecific polymorphism in external anatomy, and type specimens with unusual morphology.
Biology and life sciences – Biochemistry – Bioenergetics – Energy-producing organelles – Mitochondria – Nucleic acids – DNA – Forms of DNA – Mitochondrial DNA – Cell biology – Cellular structures and organelles – Energy-producing organelles – Mitochondria – Organisms – Eukaryota – Animals – Vertebrates – Amphibians – Frogs – Xenopus – Genetics – DNA – Forms of DNA – Mitochondrial DNA – Genomics – Animal genomics – Amphibian genomics – Genome analysis – Population genetics – Phylogeography – Biogeography – Phylogeography – Evolutionary biology – Population genetics – Phylogeography – Evolutionary systematics – Phylogenetics – Phylogenetic analysis – Population biology – Population genetics – Phylogeography – Taxonomy – Evolutionary systematics – Phylogenetics – Phylogenetic analysis – Computational biology – Genome analysis – Research and analysis methods – Animal studies – Experimental organism systems – Model organisms – Xenopus – Animal models – Xenopus – Model organisms – Xenopus – Database and informatics methods – Bioinformatics – Sequence analysis – DNA sequence analysis – Ecology and environmental sciences – Biogeography – Phylogeography – Earth sciences – Geography – Biogeography – Phylogeography – Computer and information sciences – Data management – Taxonomy – Evolutionary systematics – Phylogenetics – Phylogenetic analysis
Alpha taxonomy–the discovery and naming of species–is the linchpin of our catalog of biodiversity. Accurate species identification and diagnosis allows us to study change in populations, species, and communities, better understand how evolution occurs, and explore processes that drive diversification, extinction, and adaptation. Species names are generally assigned by the first publication to describe them, and rules exist for naming, revising, and synonymizing species names–for example as defined for animals by the International Code of Zoological Nomenclature (http://iczn.org/). One specimen, or a series of specimens, is designated to serve as a reference (a “type”) that defines a species. In principle, comparison to type specimens allows one to attribute non-type specimens to a named species, or alternatively, to justify the recognition of a new species.
Taxonomic ambiguities may arise when type material is lost or destroyed, when intraspecific variation is high, when different species have undifferentiated morphology, and when new categories of data are collected, such as nucleotide sequences, which are difficult to assay in type material. An example of one such ambiguity is the case of Fraser’s clawed frog, Xenopus fraseri. In 1852, two frog specimens collected by Louis Fraser (1819/20–1883; British zoologist and collector) were added to the catalog of the British Museum of Natural History (BMNH; now the Natural History Museum); in 1905, G. A. Boulenger designated these specimens to be syntypes of a new species, Xenopus fraseri . The two type specimens of X. fraseri (probably males) are distinguished from all other Xenopus species by the combined presence of two morphological characters: (1) vomerine teeth, found only in these type specimens, X. muelleri, and X. fischbergi, and (2) prehallux claws, present in these type specimens but not in X. muelleri or X. fischbergi, and present in several other species that lack vomerine teeth (e.g., X. allofraseri, X. parafraseri) [2, 3]. The geographic origin of X. fraseri type specimens is listed in the BMNH catalog as “West Africa” and inferred to be Nigeria or “Fernando Po” (= Bioko Island, Equatorial Guinea) , or southern Benin or southwestern Nigeria . The name X. fraseri was previously applied to populations now recognized as X. allofraseri and X. parafraseri (e.g., [3, 4]), but the combined presence of vomerine teeth and prehallux claws distinguish the syntypes of X. fraseri from these species . A third formalin-preserved specimen that was collected in northwestern Ghana in 1975 (CAS 146198; male) was tentatively assigned to X. fraseri based on external morphology . Thus, while distinctive molecular variation in the mitochondrial and nuclear genomes distinguishes all other species of African clawed frogs from one another (e.g., ), genetic data are lacking from X. fraseri because only two (or possibly three) specimens have been identified, and these are either old or formalin-preserved, and none has associated genetic samples. It thus remains unclear whether X. fraseri is in fact a distinctive species, or alternatively whether one of the more recently described species (e.g., ) is a synonym of X. fraseri. This latter possibility could arise, for example, if there is intraspecific polymorphism in the presence of either of the two morphological characters that distinguish X. fraseri types from all other species. Furthermore, if X. fraseri is distinct from other described species, both its phylogenetic position and geographic range remain unknown.
An increased understanding of Xenopus species diversity is important for several reasons. At the most basic level, an accurate inventory of species and their distributions allows us to monitor our planet’s biosphere, including how diversification and extinction vary over time and space. There are also several implications for our understanding of evolution by allopolyploidization, and by extension, the genomic dynamics of duplicate genes. Other than the diploid X. tropicalis, all species of Xenopus are allopolyploid, including 16 allotetraploid, seven allooctoploid, and four allododecaploid species . These diverse species of African clawed frogs evolved by “regular” speciation, where one ancestor diverges into two descendants, and also by “allopolyploid” speciation, where two ancestral species merge into one allopolyploid descendant species . Interestingly, allopolyploidization happened independently several times in this group, and phylogenetic analyses point to the existence of three diploid and three tetraploid species that (1) existed in the past, (2) contributed their genomes to extant tetraploid, octoploid, or dodecaploid species, and (3) do not have a known descendant with the same ploidy level as the pre-allopolyploidization ancestral species [2, 6–8]. These postulated species are the “lost ancestors” of Xenopus polyploids [2, 6–8], and any newly identified Xenopus species has the potential to be one of these lost ancestors. Discovery of one or more of these lost ancestral species could open up fascinating avenues of research that explore dynamics between each half (subgenome) of an allopolyploid genome, including mobility and suppression of transposable elements, Dobzhansky-Muller interactions, recombination, pseudogenization, subfunctionalization, and neofunctionalization (reviewed in ). Such studies would be catalyzed by currently available resources for Xenopus genomics, including two high quality genome sequences [9, 10] and powerful tools for gene editing (e. g., ).
Thus, to further understand the species status, phylogenetic placement, and geographic distribution of X. fraseri, we used sensitive techniques to capture and sequence almost complete mitochondrial genomes from both X. fraseri type specimens and the putative conspecific specimen. For comparative purposes, we also generated complete or almost complete mitochondrial DNA genomes from all other Xenopus species, and we analyzed external and internal morphology, including micro computed tomographic (μCT) scans of a X. fraseri type specimen, a putative conspecific, and populations of another Xenopus species (X. fischbergi, inferred to be closely related to X. fraseri by our phylogenetic analysis). We also followed up our phylogenetic inferences from complete mitochondrial DNA genomes, with Sanger sequencing of mitochondrial DNA from specimens we collected in the field. Our findings resolve the taxonomic quagmire presented by Mr. Fraser’s frog by establishing X. fraseri as a distinct species that occurs in northern Ghana and northern Cameroon, and is the sister taxon to X. fischbergi.
Materials and methods
Targeted high-throughput sequencing of mitochondrial genomes
We used targeted high-throughput sequencing to obtain complete or almost complete mitochondrial genome sequences from all Xenopus species, including both of the ~170-year-old type specimens of X. fraseri. We additionally obtained a partial mitochondrial genome sequence from the putative conspecific specimen of X. fraseri (CAS 146198) and an almost complete mitochondrial genome sequence from an unusual specimen of Xenopus (MZUF 16294) that was purportedly collected in Eritrea. We also used Sanger sequencing to generate partial mitochondrial sequences from recently collected specimens of X. fischbergi individuals from Chad and the Democratic Republic of the Congo, and X. fraseri individuals from northern Ghana and northern Cameroon. Apart from the putative conspecific specimen of X. fraseri (CAS 146198), the partial mitochondrial DNA sequences spanned portions of the cytochrome c oxidase I gene, the 12S and 16S ribosomal RNA genes, and the intervening tRNAval. Sample information is presented in S1 Table, and details of genetic data and capture probes, are provided in S1 Supporting Information.
Long-term storage of the four museum specimens studied here was in 60–70% ethanol or denatured alcohol, but the initial preservation treatments differed. Although we do not know what protocol was followed by Mr. Fraser when he collected the lectotype and the paralectotype specimens of X. fraseri (BMNH 19126.96.36.199 and BMNH 19188.8.131.52, formerly BMNH 18184.108.40.206 and BMNH 18220.127.116.11, respectively), it is likely that they were never exposed to formalin because the BMNH did not use formalin until the 1940s – 1950s (Colin McCarthy, personal communication). Liver and leg muscle were sampled from these specimens through small incisions made in the skin; the liver samples were used for targeted high-throughput sequencing. The putative conspecific specimen of X. fraseri (CAS 146198) was initially preserved in formalin; a sample of liver tissue from this specimen was used. A fourth museum specimen (MZUF 16294) was probably also initially preserved with formalin; a sample of muscle tissue from this specimen was used. The fourth museum specimen, a female, was listed as originating from Tessenei, Eritrea, and collected by M. Levrini in 1956. This specimen was included because the morphology was unusual for this locality because the specimen has claws on three toes of each hind foot, but the only known species in Eritrea–X. clivii–has four (including one on the prehallux). This specimen also served as a technical replicate for the performance of our targeted high-throughout sequencing on formalin preserved tissues.
Assembly and inference of complete mitochondrial genomes
Reads were demultiplexed based on exact matches to sample-specific barcodes. Overlapping paired-end reads were then merged into consensus reads when possible. A de novo assembly of the complete mitochondrial genome was attempted for each sample with Trinity version 2.5.1 . The advantage of a de novo assembly over a reference-based assembly is that the former approach may more accurately reconstruct insertion deletion polymorphisms, and presumably is less biased by a reference sequence.
The de novo assembly produced one ~17kb contig for the entire mitochondrial genome for almost all of the non-museum samples (28 out of 29), but none of the museum samples. For 5 of the 29 non-museum samples (X. tropicalis, X. mellotropicalis, X. victorianus, X. laevis, and X. wittei) the initial de novo assembly produced an assembly with two concatenated mitochondrial genomes. One sample (X. poweri) produced a fragmented assembly, and one of the two X. boumbaensis samples assembled only a small portion of the mitochondrial genome. For the five samples that initially produced concatenated mitochondrial genomes assembly, the de novo assembly was repeated using a k-mer size equal to either 21 or 32 instead of the initial setting of 29. For X. victorianus and X. mellotropicalis, a k-mer size equal to 21 provided a non-concatenated assembly, and the same for X. laevis and X. wittei with a k-mer size equal to 32. For X. poweri, the assembly was fragmented into 4 contigs that were independently aligned to the other de novo genomes with the others using Mafft  using the “—adjustdirection” option to align reverse-complemented contigs. The X. poweri sequence was then concatenated manually into a complete genome. For the X. boumbaensis sample that did not fully assemble de novo, we instead used the other X. boumbaensis de novo mitochondrial genome sequence as a reference, and generated a consensus sequence from reads that were mapped to this reference as described below for the museum samples.
Because de novo assembly of the museum samples failed to produce a complete mitochondrial genome, we instead generated a consensus sequence from unique and de-duplicated reads from each sample that were mapped to a reference mitochondrial genome. For each sample, we explored the effect of mapping to three different reference genomes that we generated de novo (X. laevis, X. parafraseri, X. fischbergi). We used as a reference the genome that yielded the most complete consensus, which was the X. fischbergi mitochondrial genome for the X. fraseri lectotype and paralectotype specimens, for the putative X. fraseri conspecific, and the X. laevis mitochondrial genome for the Eritrea specimen. Consensus calling on mapped reads requiring a coverage of at least 5x for each base, at least 80% agreement of the genotype, and a minimum map quality of 25.
To evaluate the phylogenetic position of the mitochondrial genome sequences from X. fraseri, we performed phylogenetic analysis on these sequences along with previously published mitochondrial genome sequences of several species in Pipoidea (the clade that contains the sister families Rhinophrynus and Pipidae) including Rhinophrynus dorsalis (HM991334.1), Pipa carvalhoi (HM991332.1) and P. pipa (GQ244477.1), Hymenochirus boettgeri (HM991331.1), and Pseudhymenochirus merlini (HM991333.1), X. cf. tropicalis (AP014695), X. tropicalis (AY789013), and X. borealis (JX155859). We excluded four regions from the alignment of these data where we deemed homology to be ambiguous based on visual inspection. These regions included the entire tRNAPro and D-loop (positions 15,500–17,610 of AY789013.1), two portions of the 16S rDNA gene (positions 1099–1140 and 2214–2228 of AY789013.1), and a portion of the origin for light strand replication (positions 5231–5248 of AY789013.1). To explore the effects of missing data, we performed separate phylogenetic analysis on an alignment that included only the complete or almost complete mitochondrial DNA genomes, and on an alignment that included these data plus the partial mitochondrial DNA genome sequences (S1 Table, S1 Supplemental File).
IQ-TREE version 1.6.8 [14, 15] was used for maximum likelihood phylogenetic analysis and model selection (the GTR+F+I+G4 model was selected for both datasets–with and without the partial mitochondrial sequences–according to the Bayesian Information Criterion), and ultrafast bootstrap analysis (with 1,000 replicates) was used to assess support for this topology. We also analyzed the both datasets with BEAST version 2.52 , using the same model of evolution listed above, a Yule model for the tree prior, and assuming an uncorrelated lognormal relaxed molecular clock. Three calibration points were used, all with a normally distributed prior probability distribution, and all following estimates in : (1) the age of genus Xenopus, which subtends the subgenera Silurana and Xenopus , was set to a mean of 45.3 million years (my), and a standard deviation of 5.7 my, (2) the age of family Pipidae was set to a mean of 117.6 and a standard deviation of 6.6 my, and (3) the age of Pipoidea was set to a mean of 159.4 my and a standard deviation of 6.0 my. For each BEAST analyses, 4 or 8 independent runs were performed respectively, each for 10 million generations, sampling every thousand generations, and starting from a random tree. Twenty-five percent of each run was discarded as burn-in. Tracer version 1.71  was used to verify that the effective sample sizes of all parameters exceeded 200.
We previously collected high-resolution X-ray μCT scans of several Xenopus specimens, including the paralectotype of X. fraseri and the holotype of X. fischbergi . We used the same methodology to generate a scan of the putative X. fraseri specimen from Ghana (CAS 146198) and several more specimens of X. fischbergi, including one adult of each sex and two juveniles from Chad (specimens AMNH-H-A158343, AMNH-H-A158360, AMNH-H-A158350, and AMNH-H-A158356). These specimens were selected to capture variation between the sexes and during development. We lacked data from these post-metamorphic individuals from Chad, but inferred them to be X. fischbergi based on sequence from another individual (a tadpole) that was collected at the same time and localition (AMNH A-158377; S1 Table). We additionally examined external morphology and measured snout-vent lengths from several individuals for which we had sequence data to confirm species identification as X. fraseri or X. fischbergi (the sister taxon of X. fraseri, see below), and we also took measurements from the two adult X. fischbergi specimens from Chad.
All procedures involving live animals have been approved by the Animal Use Committee at McMaster University (AUP 17-12-43).
Xenopus fraseri is distinct from all other species, the sister species of X. fischbergi, and minimally distributed in northern Ghana and northern Cameroon
Using targeted high-throughput sequencing, we obtained complete or almost complete mtDNA sequences from at least one representative of all Xenopus species, and including three of the four museum samples, and including both of the type specimens of X. fraseri (average length of all but CAS 146198 was 17,192 base pairs (bp), the range was 14,204–17,833 bp). A partial (5,930 bp) mitochondrial genome sequence was obtained from the more recently collected putative X. fraseri specimen from Ghana (CAS 146198). Phylogenetic analysis of these genomes indicates that mitochondrial DNA from both type specimens of X. fraseri are closely related, substantially diverged from other Xenopus species, and sister to mitochondrial sequences of X. fischbergi (Fig 1, S1 Fig).
Analysis of complete or almost complete mitochondrial DNA genomes were inferred by Bayesian and maximum likelihood phylogenetic methods identified no strongly supported topological differences, and most nodes had strong posterior probability and bootstrap support (Fig 1, S1 Fig). The BEAST analysis indicates that the mitochondrial genomes of X. fraseri and X. fischbergi diverged ~4.7 million years ago (mya; 95% highest probability density interval 2.8–7.1 mya).
These findings in mind, we then examined other wild-caught individuals sampled throughout the putative ranges of X. fischbergi and X. fraseri in five countries in West and Central Africa: the Democratic Republic of the Congo, Cameroon, Nigeria, Chad, and Ghana. Phylogenetic analysis of partial mitochondrial DNA Sanger sequences from these individuals combined with the mitochondrial genome sequences described above demonstrates that X. fraseri is distributed in northern Ghana and northern Cameroon, including CAS 146198, whereas X. fischbergi occurs in the Democratic Republic of the Congo, Chad, and Nigeria (Fig 1, S1 Fig). In both of these analyses (complete mitochondrial genomes with or without the partial sequences), the phylogenetic position of X. fraseri places it unambiguously within the muelleri species group, which includes as well X. muelleri, X. borealis, and X. fischbergi . The relatively recent divergence of X. fraseri within the muelleri species group indicates that it is not one of the lost ancestors, and suggests that X. fraseri could be an allotetraploid species with 36 chromosomes, although we did not generate a karyotype to assess this.
Divergence in mitochondrial DNA
Molecular divergence between the mtDNA sequences of the lectotype and paralectotype of X. fraseri was low: the uncorrected pairwise divergence (hereafter, divergence) was 0.11% out of 13,909 non-missing and non-gapped base pairs (hereafter, positions). Divergence between each of these sequences and the putative X. fraseri conspecific was also low: 0.22% out of 5,889 positions. But the complete genome of X. fischbergi from Nigeria was substantially diverged from almost complete mitochondrial genomes of the lectotype and paralectotype specimens of X. fraseri (4.37% or 4.53% out of 13,959 or 15,350 positions, respectively) and 2.7% diverged from the partial mitochondrial genome from the putative X. fraseri conspecific (out of 5889 positions). The smaller portions of the mitochondrial genome of X. fischbergi from Chad were also substantially diverged from the lectotype and paralectotype specimens of X. fraseri individuals (3.43% and 3.59% out of 2,796 or 2,842 positions, respectively) and from the partial mitochondrial genome from the putative X. fraseri conspecific (2.35% out of 2003 positions).
These divergences between X. fraseri and X. fischbergi exceed that between several other allotetraploid Xenopus sibling species pairs such as Xenopus petersii and X. victorianus (these two species are 3.43% diverged over their whole mitochondrial genomes, 1.87% over the portion of the genome that was sequenced for the putative X. fraseri conspecific, and 1.36% over the portion of the mitochondria that was sequenced for the X. fischbergi individual from Chad). Divergences between various dodecaploid species pairs (e.g., X. kobeli and X. ruwenzoriensis) are even lower than that observed between X. petersii and X. victorianus (Fig 1, S1 Fig). Divergence among mitochondrial DNA of X. tropicalis and X. cf. tropicalis is considerably larger than most other species owing to an unusual haplotype from Liberia [19, 20] that may constitute a distinct species  (with caveats based on one nuclear gene [2, 21]).
Role of reference genome in consensus sequences
Although most of the mitochondrial genomes reported here were assembled de novo, the mitochondrial DNA genomes for the museum samples were generated by mapping capture data to a closely related reference genome. A possible concern with this approach is that the reference-based consensus sequences for the museum samples might be affected by which reference genome was used. To explore this, we compared the consensus sequences from each X. fraseri type specimen that were generated when either X. fischbergi or X. laevis was used. This comparison demonstrated that the consensus sequences were minimally biased, and far more complete when a closely related reference genome was used compared to a more distantly related reference genome (Supplemental Results). Our analyses suggest that the reference genome imposes only a modest bias on consensus sequences, but to the extent that it does, our figures for divergence between the mitochondrial genomes of X. fraseri and X. fischbergi may be slight underestimates.
Comparison of external and internal anatomy of the putative X. fraseri conspecific CAS 146198 to the X. fraseri paralectotype (BMNH 1918.104.22.168) and the holotype of X. fischbergi (CAS 255060) confirms the presence of vomerine teeth (insets in Fig 2). A pointed keratinized prehallux claw is absent in X. fischbergi and appears to be an intraspecific polymorphism in X. fraseri that distinguishes some specimens of X. fraseri from specimens of other species (Supplementary Results; S2 Fig). The small size (for the muelleri species group ) of the lectotype and paralectotype of X. fraseri and the X. fraseri from Ghana (S2 Table) could suggest that they are not fully mature. However, examination of 13 other adult X. fraseri individuals from Ghana indicates that this species is indeed substantially smaller than X. fischbergi. The average SVLs of seven adult female and six adult male X. fraseri were 46.8 mm and 38.5 mm, respectively (ranges 39.9–54.2 and 36.9–32.5 mm respectively; S2 Table). The average SVL of the holotype and two paratypes (all female) of X. fischbergi, and two other female specimen from the Democratic Republic of the Congo (UTEP21194), is 57.8 mm (S2 Table), which is 25% larger than the X. fraseri females we measured. An adult male X. fischbergi we measured was larger than all seven males of X. fraseri that we measured (S2 Table).
Subtle differences in skeletal morphology are suggested by μCT scans. In the ventral view, the optic foramina of the X. fischbergi holotype and other specimens have more rounded margins on the fronto-parietal bone, especially in the adult specimens, compared to the X. fraseri paralectotype and putative conspecific (Fig 2, S3 Fig). However, the small sample of μCT scans prevents us from assessing whether these differences are distinctive in each species.
Other phylogenetic insights
Our analysis of complete mitochondrial genome sequences from all Xenopus species provides strong statistical support for several novel or previously poorly supported relationships among mitochondrial DNA lineages in Xenopus (e.g., ), including strong support for (i) a sister relationship between X. largeni and a clade comprising mitochondrial lineages of species in the laevis and amieti species groups, and methodologically variable support (strong for Bayesian but modest for maximum likelihood) for (ii) a sister relationship between mitochondrial DNA from (X. lenduensis + X. vestitus) and species in the laevis species group, that renders mitochondrial DNA of the amieti group paraphyletic, and (iii) a sister relationship between X. clivii and species in the muelleri group (including X. fraseri). The complete mitochondrial genome from a museum specimen that was reportedly collected in Eritrea (MZUF 16294) was essentially identical to a complete mitochondrial genome from X. laevis from South Africa. This suggests that this specimen either was introduced to Eritrea from southern Africa where X. laevis occurs, or (we suspect) was mislabeled, and actually originated from South Africa. This specimen indicates that formalin preserved material has the potential to yield complete mitochondrial DNA genomes, even though we did not obtain one from CAS 146198.
Although we do not advocate using divergence of mitochondrial DNA as the sole justification for species distinctiveness, these data coupled with morphological characteristics discussed above, including the substantially smaller size of X. fraseri compared to other closely related species (S2 Table, ), and a pointed prehallux in some X. fraseri individuals, argues for the distinctiveness of X. fraseri. The specimens of X. fraseri were sampled from 4 different localities, and internal examination of one female indicated that she was gravid. This suggests the smaller size of these individuals compared to X. fischbergi is unlikely to be due to ontogeny. Our findings indicate that the sister taxon of X. fraseri is X. fischbergi, and that X. fraseri is a member of the muelleri species group along with X. muelleri, X. fischbergi, and X. borealis (Fig 1, S1 Fig). The minimal distribution of X. fraseri, established in this study, is in northern Ghana and Cameroon. Xenopus fraseri may be partially sympatric with X. fischbergi, the latter of which ranges at least from Nigeria to the northern Democratic Republic of the Congo (based on mitochondrial sequences), and possibly even farther west and east of this . Given the similarity in external morphology of X. fraseri and X. fischbergi, our previous delineation of the range of X. fischbergi  may be an overestimate and, based on genetic information, we reassign several paratypes of X. fischbergi to X. fraseri, as detailed in the Supplemental Results.
Our recent systematic revision of West African Xenopus  included sequence data from two genetic samples that were identified here to be X. fraseri, but we failed to identify them then as being distinctive from X. fischbergi . At that time, we did not realize that the shape and morphology of the prehallux was so variable within X. fraseri. The prehalluxes of the X. fraseri types and the formalin-preserved specimen from Ghana (CAS 146198) are the most keratinized specimens we have encountered (S2 Fig), so the type specimens of X. fraseri are in fact not particularly “typical” of this species in this regard. Additionally, because the mitochondrial DNA data in  was from a relatively slowly evolving portion of this genome, the divergence between the X. fraseri and X. fischbergi data in  was lower (~3%) than that between the almost complete mitochondrial genomes that were generated for this study (>4%; Supplemental Results).
In species with low dispersal rates, divergent and geographically separated intra-specific clades with narrow regions of overlap may arise without geographic barriers to gene flow ; this is seen, for example, in X. laevis from southwest South Africa . In contrast, it is rare in species with low dispersal rates–including in Xenopus –for diverged intra-specific clades of mitochondrial DNA to have broadly overlapping geographic distributions. This phylogeographic pattern is instead suggestive of cryptic species [2, 23], and the new genetic and morphological information from X. fraseri presented here allowed us to distinguish this cryptic species from another closely related, morphologically similar, and possibly co-distributed or parapatric species (X. fischbergi).
Other phylogenetic insights
The inference of a closer phylogenetic affinity of the mitochondrial genome of X. clivii to the mitochondrial genomes of the muelleri species group than to those of the laevis or amieti species groups is in line with inferences based on complete transcriptomes . This observation is of interest for studies of sex chromosomes because X. clivii and several species in the laevis and amieti species group carry the female-specific sex determining gene dm-w , whereas X. borealis does not carry dm-w, and has a newly evolved sex chromosome [26, 27]. This phylogenetic relationship of mitochondrial DNA, which is (also) maternally inherited, indicates that dm-w was lost at some point in the ancestry of X. borealis after the divergence of X. clivii .
Because he died over a century ago, Mr. Fraser is unavailable to tell us exactly where he collected his frog. Despite the uncertainty over the origin of Mr. Fraser’s specimens, it has long been assumed that X. fraseri is distributed in lowland tropical forest . This was reinforced by the many records of morphologically similar forest-dwelling specimens, including those now called X. parafraseri and X. allofraseri . In fact, X. fraseri is distributed in relatively hot, arid savanna, including the borders of the Sahel. We argued previously based on historical records that the lectotype and paralectotype specimens of X. fraseri were probably collected in southern Benin or southwestern Nigeria  in areas that are in or near the Dahomey Gap, an area of savanna extending south from the Sahel that subdivides tropical rainforest habitat of West Africa, and that is poorly studied for Xenopus. Consistent with this proposal, the localities of this species identified here–northern Cameroon and northern Ghana–are in the same ecoregions as the Dahomey Gap (West Sudanian savanna and Guinean forest-savanna mosaic) . Previous confusion about X. fraseri arose as a consequence of poor records of the provenance of the type specimens, the generally conserved interspecific morphology of several Xenopus species, high-intraspecific polymorphism of the prehallux of X. fraseri, and the unusual prehallux morphology of the X. fraseri type specimens. This study thus provides clarity to this taxonomic enigma presented by Fraser’s frog by identifying distinctive molecular and morphological features of this species–as well as polymorphic aspects, and by delineating its phylogenetic position and geographic distribution.
1. Boulenger GA. On a collection of batrachians and reptiles made in South Africa by Mr. C. H. B. Grant, and presented to the British Museum by Mr. C. D. Rudd. Proceedings of the Zoological Society of London. 1905;1905:248–55.
2. Evans BJ, Carter TF, Greenbaum E, Gvoždík V, Kelley DB, McLaughlin PJ, et al. Genetics, morphology, adverstisement calls, and historical records distinguish six new polyploid species of African clawed frog (Xenopus, Pipidae) from West and Central Africa. PLoS One. 2015;10(12):e0142823. doi: 10.1371/journal.pone.0142823 26672747
3. Kobel HR, Loumont C, Tinsley RC. The extant species. In: Tinsley RC, Kobel HR, editors. The Biology of Xenopus. Oxford: Clarendon Press; 1996. p. 9–33.
4. Conlon JM, Mechkarska M, Kolodziejek J, Nowotny N, Coquet L, Leprince J, et al. Host-defense peptides from skin secretions of Fraser's clawed frog Xenopus fraseri (Pipidae): Further insight into the evolutionary history of the Xenopodinae. Comparative Biochemistry and Physiology, Part D Genomics Proteomics. 2014;12:45–52. doi: 10.1016/j.cbd.2014.10.001 25463057
5. Evans BJ. Genome evolution and speciation genetics of allopolyploid clawed frogs (Xenopus and Silurana). Front Biosci. 2008;13:4687–706. 18508539
6. Evans BJ, Carter TF, Hanner R, Tobias ML, Kelley DB, Hanner R, et al. A new species of clawed frog (genus Xenopus), from the Itombwe Plateau, Democratic Republic of the Congo: Implications for DNA barcodes and biodiversity conservation. Zootaxa. 2008;1780:55–68.
7. Evans BJ, Greenbaum E, Kusamba C, Carter TF, Tobias ML, Mendel SA, et al. Description of a new octoploid frog species (Anura: Pipidae: Xenopus) from the Democratic Republic of the Congo, with a discussion of the biogeography of African clawed frogs in the Albertine Rift. J Zool, Lond. 2011;283:276–90.
8. Evans BJ, Kelley DB, Tinsley RC, Melnick DJ, Cannatella DC. A mitochondrial DNA phylogeny of clawed frogs: Phylogeography on sub-Saharan Africa and implications for polyploid evolution. Mol Phylogenet Evol. 2004;33:197–213. 15324848
9. Session AM, Uno Y, Kwon T, Chapman JA, Toyoda A, Takahashi S, et al. Genome evolution in the allotetraploid frog Xenopus laevis. Nature. 2016;538(7625):336–43. doi: 10.1038/nature19840 27762356; PubMed Central PMCID: PMC5313049.
10. Hellsten U, Harland RM, Gilchrist MJ, Hendrix D, Jurka J, Kaptonov V, et al. The genome of the western clawed frog Xenopus tropicalis. Science. 2010;328:633–6. doi: 10.1126/science.1183670 20431018
11. Tandon P, Conlon F, Furlow JD, Horb ME. Expanding the genetic toolkit in Xenopus: Approaches and opportunities for human disease modeling. Dev Biol. 2016;426(2):325–35. doi: 10.1016/j.ydbio.2016.04.009 27109192.
12. Grabherr MG, Haas BJ, Yassour M, Levin JZ, Thompson DA, Amit I, et al. Full-length transcriptome assembly from RNA-Seq data without a reference genome. Nat Biotechnol. 2011;29(7):644–52. doi: 10.1038/nbt.1883 21572440; PubMed Central PMCID: PMC3571712.
13. Katoh K, Standley SM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. MBE. 2013;30:772–80.
14. Minh BQ, Nguyen MA, von Haeseler A. Ultrafast approximation for phylogenetic bootstrap. Mol Biol Evol. 2013;30(5):1188–95. doi: 10.1093/molbev/mst024 23418397; PubMed Central PMCID: PMC3670741.
15. Nguyen LT, Schmidt HA, von Haeseler A, Minh BQ. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol Biol Evol. 2015;32(1):268–74. doi: 10.1093/molbev/msu300 25371430; PubMed Central PMCID: PMC4271533.
16. Drummond AJ, Suchard MA, Xie D, Rambaut A. Bayesian phylogenetics with BEAUti and the BEAST 1.7. MBE. 2012;29:1969–73.
17. Feng YJ, Blackburn DC, Liang D, Hillis DM, Wake DB, Cannatella DC, et al. Phylogenomics reveals rapid, simultaneous diversification of three major clades of Gondwanan frogs at the Cretaceous-Paleogene boundary. PNAS. 2017;114(29):E5864–E70. doi: 10.1073/pnas.1704632114 28673970; PubMed Central PMCID: PMC5530686.
18. Rambaut A, Drummond AJ. Tracer v1.5, Available from http://beast.bio.ed.ac.uk/Tracer. 2007.
19. Haramoto Y, Oshima T, Takahashi S, Asashima M, Ito Y, Kurabayashi A. Complete mitochondrial genome of “Xenopus tropicalis” Asashima line (Anura: Pipidae), a possible undescribed species. Mitochondrial DNA. 2016;6(27):3341–3.
20. Evans BJ, Cannatella DC, Melnick DJ. Understanding the origins of areas of endemism in phylogeographic analyses: a reply to Bridle et al. Evolution. 2004;58(6):1397–400.
21. Evans BJ, Kelley DB, Melnick DJ, Cannatella DC. Evolution of RAG-1 in polyploid clawed frogs. MBE. 2005;22(5):1193–207.
22. Irwin DE. Phylogeographic breaks without geographic barriers to gene flow. Evolution. 2002;56(12):2383–94. 12583579
23. Furman BL, Bewick AJ, Harrison TL, Greenbaum E, Gvozdik V, Kusamba C, et al. Pan-African phylogeography of a model organism, the African clawed frog 'Xenopus laevis'. Mol Ecol. 2015;24(4):909–25. doi: 10.1111/mec.13076 25583226.
24. Bickford D, Lohman DJ, Sodhi NS, Ng PKL, Meier R, Winkley K, et al. Cryptic species as a window on diversity and conservation. TREE. 2006;22(3):148–55. 17129636
25. Furman BLS, Evans BJ. Sequential turnovers of sex chromosomes in African clawed frogs (Xenopus) suggest some genomic regions are good at sex determination. G3. 2016;6:3625–33. doi: 10.1534/g3.116.033423 27605520
26. Yoshimoto S, Okada E, Umemoto H, Tamura K, Uno Y, Nishida-Umehara C, et al. A W-linked DM-domain gene, DM-W, participates in primary ovary development in Xenopus laevis. PNAS. 2008;105(7):2469–74. doi: 10.1073/pnas.0712244105 18268317
27. Bewick AJ, Anderson DW, Evans BJ. Evolution of the closely related, sex-related genes DM-W and DMRT1 in African clawed frogs (Xenopus). Evolution. 2011;65(3):698–712. doi: 10.1111/j.1558-5646.2010.01163.x 21044062
28. Tinsley RC, Loumont C, Kobel HR. Geographical distribution and ecology. In: Tinsley RC, Kobel HR, editors. The Biology of Xenopus. Oxford: Clarendon Press; 1996. p. 35–59.