Introduction

Species extinction is occurring at an unprecedented rate1, brought about by human-induced habitat loss, overexploitation for economic gain, and climate change. Notwithstanding the urgent need to address the causes of this catastrophic decline in biodiversity, we must understand that many species could be lost before they or their significance have been recognised by science. We are unaware of what it is we are losing. Taxonomic research is arguably more important today than it has been at any time in its history.

Taxonomy has as its foundation the concept of diagnosability. Each new taxon is formally described by identifying one or more traits that consistently distinguish it from other closely related taxa. According to the International Code of Zoological Nomenclature, the name of any new species is unambiguously linked to and defined by the so-called name bearing type specimen. Each generation of taxonomists must deal with new information, brought about by advances in technologies and the discovery of new informative traits. Often they must gather that new information from specimens used by previous generations of taxonomists in making their determinations2. Name-bearing type specimens for each named species, and making the types widely available through museums, are thus the foundation of taxonomic enquiry.

DNA technologies have revolutionized taxonomy by bringing to the table a large suite of new characters to complement those available from morphological analysis. At the same time, DNA technology presents a challenge because rarely can the new information be obtained for types used by previous taxonomists. Type specimens are either fixed in formalin, a process that cross-links the DNA with associated proteins and renders the DNA inaccessible, or they are preserved in such a way that DNA is degraded. As a consequence, the accelerating rate at which new biodiversity is being documented is somewhat disconnected from the taxonomic work that has taken place before. Uncertainty over the identity of new forms in comparison to historical type specimens can lead to considerable confusion and taxonomic instability. Generating DNA sequences from historical material has been a major challenge, but the advent of high-throughput parallel sequencing and ancient or trace DNA (aDNA) approaches have fundamentally altered the situation. Although still not routine, generating historical DNA data has become feasible on a large scale3,4,5,6. DNA sequencing of name-bearing type specimens is thus regarded as the gold standard for taxonomy7, because it enables unambiguous assignment of extant populations to the named entity or enables a clear distinction between newly discovered forms and those that have already been described.

Australia is the smallest of all continents and congruent with the nation of the same name. As an island continent, isolated by sea from other vegetated continents for 65 My, it is well known for its endemic fauna and flora. With approximately 755 species, Australia’s reptile diversity exceeds that of any other country for this group8. Turtles constitute an iconic group among reptiles that is represented in Australia mostly by the family Chelidae (suborder Pleurodira), side-necked turtles of Gondwanan origin and occurring elsewhere only in New Guinea, on the islands of Roti and Timor of Indonesia and Timor Leste, and in South America9. All chelids are freshwater turtles. As the driest vegetated continent on earth, Australia harbours fewer freshwater turtle species than the Americas or Asia. Together with the chelid species from New Guinea, Roti and Timor, there are 36 Australasian species belonging to this family9,10. The Australian chelid species often directly compete with humans for water resources and habitat, making their long-term conservation a challenge. For any conservation planning, a sound taxonomy is the necessary prerequisite.

Compared to other continents, the Australasian turtle fauna is poorly known and significant progress has been made only recently10,11,12,13,14,15,16,17,18,19,20,21. Taxonomic assessment of Australasian chelids is impeded by two issues. One is the publication of scientific names in outlets circumventing scientific peer review and contributing to massive confusion by the creation of ill-defined taxa and an alternative competing nomenclature10,22,23. The other issue derives from the fact that many historical species descriptions used type specimens without or only with vague locality data, making the identification, and thus the naming, of genetically identified clusters difficult to impossible14,24. In addition, the identity of some recently described chelid taxa is unclear (Chelodina gunaleni, C. kuchlingi, C. mccordi mccordi, C. m. roteensis, C. m. timorlestensis, C. m. timorensis) and multiple names could refer to the same taxon9,10.

Here we present almost complete mitochondrial genomes for 18 crucial name-bearing type specimens of chelid turtles, and combine this evidence with new mitogenomes of other Australasian chelids and mitogenomes available from GenBank. We use these data to address longstanding controversies arising from uncertainty in the taxonomic identity of historical type specimens. The oldest type specimen sequenced dates back to the late 18th century (Testudo longicollis Shaw)25. Using whole mitochondrial sequencing, we show the value of generating sequences from historical type specimens in resolving contemporary controversies in taxonomy.

Materials and Methods

Sample preparation

Muscle tissue was sampled from the thigh of alcohol-preserved type specimens (Table S1); tissue from dry specimens, from inside the shell or the inguinal region of the shell. Fresh material (Table S2) was obtained from turtles sampled alive by cutting a sliver of skin from the trailing web of the hind foot or by sampling blood from the jugular vein in accordance with the “Standard Operating Procedures (SOPs) for the care and use of animals in laboratory studies, teaching and field research” developed by the Animal Ethics Committee of the University of Canberra. We did not conduct experiments on the live turtles, but the procedures used to sample tissue and blood were nevertheless subject to the SOP. Thus, the samples were obtained according to all relevant guidelines, regulations and best ethical and experimental practice of the University of Canberra. The blood and tissue samples were collected as part of other studies; the samples for this publication were accessed from the Wildlife Tissue Collection of the University of Canberra. No samples were specifically collected from live animals for this study.

Mitochondrial genomes for the live specimens were generated as described in Zhang et al.26. Mitochondrial genomes for the type specimens were generated by extracting DNA using commercial DNA extraction kits. Illumina libraries were prepared according to Meyer & Kircher27 as modified by Fortes & Paijmans28; preparing bait libraries and conducting two rounds of in-solution hybridization capture following the methods of Maricic et al.29 and Horn30; and sequencing on an Illumina MiSeq sequencing platform. Detailed methods are described in the Supplementary Information. To avoid cross-contamination, samples were divided into categories of historical samples and recent samples, and processed in laboratories that were physically separated. DNA extractions and Illumina library preparation for the historical samples (13 samples collected between ~1790–1990) were undertaken in the clean room facility of Senckenberg Dresden, which meets all standards of an ancient DNA laboratory as outlined in Fulton31. Fresh materials (6 samples collected between 1994–2007) were processed in the main molecular laboratory of Senckenberg Dresden. Negative controls (water blanks) were included during DNA extraction and library preparation and screened for evidence of contamination after sequencing. The remaining fresh samples were processed in the PC2 facilities at the Wildlife Genetics Laboratory at the University of Canberra.

Assembly

Demultiplexing the sequence reads and generating of the fastQ files were automatically performed by the miseq reporter 2.6.2.3. Subsequently, adapters were trimmed with skewer 0.2.232, reads merged (minimum read length 35 bp) and duplicates removed with BBMap-suite 37.24 (https://sourceforge.net/projects/bbmap/)33. Sequence length distribution of merged single reads was checked using a customized command written in awk. Subsequent visualisation used microsoft excel. Subsamples from the full readpool were created with fastq-tools v 0.8 (https://github.com/dcjones/fastq-tools) to keep the average read coverage below 200x. Assembly used the MITObim pipeline34, which uses MIRA435 in a two-step baiting and iterative mapping. The complete mitochondrial sequence of KJ713173 (Chelodina longicollis) was used as a starting seed. For each sample, three different mapping stringencies were tested, setting the allowed mismatches to 15% of the average read length (MM15, default value), to a maximum of five (MM5), and to a maximum of two (MM2). Sequence length distribution of the assembled merged reads was obtained as described above. A visual exploration of the resulting assemblies for assembly artefacts and regions of conflicts (mostly low coverage regions) was performed using tablet 1.16.09.0636. For each sample, the obtained contigs (the assembled mt-genome sequences) of the MM15 and the MM2 analyses were manually compared. If they were identical, the assembled mt-sequence was accepted. For those samples where differences occurred and obvious assembly artefacts could not be corrected by hand, a consensus sequence of the corresponding MM2 and MM5 analysis was obtained, masking all conflicting positions with Ns (ambiguous nucleotide positions). After the assembly, PCR priming sites at the 5′ and 3′ ends of the assembled mt-sequences were removed before submitting them to a BLAST search.

Each library was also analysed using the complete mitochondrial sequence of KU867578 (Homo sapiens) as a starting seed to check for human contamination.

Sequence alignment and annotation

Each mt-sequence was first annotated under default parameters using mitos37 to check gene arrangement. Then an automated pre-alignment of all sequence data was conducted using clustalw 1.4 as implemented in bioedit 7.0.9.038, with default parameters39. A final alignment adjustment and sequence annotation was performed manually, based on four published mt-genomes: AF039066 (Pelomedusa), KY486272 (Pseudemydura), KC692462 (Emydura), and KJ713173 (Chelodina). Two alignments were produced, one based on full sequences (FULL), the second on coding sequences only (CDS). Further details of the alignment and annotation are provided in the Supplementary Information.

Phylogenetic analysis and genetic distances

Phylogenetic relationships of the mitogenomes were estimated by applying RAxML 8.0.040 for Maximum Likelihood (ML), and mrbayes 3.2.641 for Bayesian inference (BI), to the CDS and FULL alignments. The selection of the best fitting evolutionary models (Tables S3, S4) and the data partitioning schemes for the analyses was computed with partitionfinder 242 using the Bayesian Information Criterion. Five different partition schemes were considered (unpartitioned—1 partition; third codon position extra, i.e., first and second codon positions combined, third codon position extra, 12 S, 16 S, control region, all tRNAs combined—6 partitions; each codon position extra, i.e., as preceding partitioning scheme except first and second codon positions extra—7 partitions; gene-partitioned, i.e., 13 coding genes, 12 S, 16 S, control region, tRNAs combined—17 partitions; codon-partitioned, i.e. 13 times 3 codon positions extra, 12 S, 16 S, control region, tRNAs combined—43 partitions). For ML and BI, the codon-partitioned dataset was selected. For ML, five independent rapid bootstrap searches were run using different starting conditions. Subsequently, 1000 non-parametric thorough bootstrap replicates were calculated and the values plotted against the best tree. Two parallel runs (each with four chains) were performed for BI for 10 million generations (burn-in fraction 0.25; print frequency 1000; sample frequency 500). The calculation parameters were analysed using the software tracer 1.7.143. Posterior probabilities were plotted onto the phylograms. MEGA744 was used for exploratory calculations of uncorrected p distances using the pairwise deletion option.

Results

In total, 52 mitochondrial genomes were analysed, including one outgroup (Pelomedusa), of which 15 were taken from GenBank and 37 (including 18 types) were newly generated (Tables S1, S2). Among the historical type specimens, only processing of the holotype of Platemys novaeguineae Meyer, 1874 failed. This specimen was boiled during the firestorm of Dresden following allied bombing in the Second World War45. Assembly information of the sequenced type specimens such as size of readpool, number of assembled reads, average coverage, and average read length of assembled reads are summarized in the Supplementary Information. The aligned data covered almost the entire mitochondrial genome, missing only part of the control region and part of the DNA coding for tRNA Phe. All samples had a typical vertebrate mitochondrial genome organisation46. For further details of the alignment (e. g., observed frame shifts in coding regions), see Supplementary Information.

Phylogeny and species assignment

The Maximum Likelihood (ML) and Bayesian inference (BI) trees for each dataset were highly consistent, with identical branching patterns and similar support values (Figs 1 and 2). Most nodes had maximum support under both tree-building methods. Placement of only one taxon, Chelodina steindachneri, differed between the phylogenies generated from the two alignments (‘FULL’ and ‘CDS’).

South American and Australasian chelids were revealed as maximally supported sister clades. Within the Australasian taxa, Pseudemydura umbrina constituted the deeply divergent sister taxon of two other deeply divergent, more inclusive clades. One of these consisted of the snake-necked and long-necked turtles of the genus Chelodina and the other comprised short-necked turtles of the genera Elseya, Elusor, Myuchelys, and Rheodytes. Many of the nominal taxa within Chelodina showed smaller genetic divergences than the taxa within the ‘short-necked clade’.

Figure 1
figure 1

Maximum Likelihood tree for chelid mitogenomes, including historical type specimens using a 16,289-bp-long alignment. For historical type specimens, the original name combinations are shown in bold. Numbers at nodes are bootstrap values and posterior probabilities for a Bayesian tree of the same topology. Asterisks indicate maximum support under both methods. Quotation marks for a GenBank sequence assigned to Emydura subglobosa (KC692462) indicate questionable taxonomic allocation. Lectotype and paralectotype of Hydraspis victoriae were previously erroneously identified. The species description was based only on the putative paralectotype, which is therefore the name-bearing holotype (see Discussion). Snake-necked species of Chelodina in red, long-necked species in black. Icons are derived from photos of Chelodina steindachneri (long-necked Chelodina), C. burrungandjii (snake-necked Chelodina), and Elusor macrurus (short-necked species; from top to bottom). Drawings: U. Fritz. On the right are for Australasian taxa the currently accepted genera shown9.

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Figure 2
figure 2

Maximum Likelihood tree for chelids, including historical type specimens using an 11,328-bp-long alignment corresponding to the 13 coding genes of the mitogenome. For historical type specimens, the original name combinations are shown in bold. Quotation marks for a GenBank sequence assigned to Emydura subglobosa (KC692462) indicate questionable taxonomic allocation. Numbers at nodes are bootstrap values and posterior probabilities for a Bayesian tree of the same topology. Asterisks indicate maximum support under both methods. Note the different placement of Chelodina steindachneri compared to Fig. 1. Snake-necked species of Chelodina in red, long-necked species in black. On the right are for Australasian taxa the currently accepted genera shown9. Inset: historical type specimen of Testudo longicollis Shaw, 1794 (photo: P. D. Campbell). For further explanation, see Fig. 1.

Full size image

Within the snake-necked and long-necked turtle clade, C. parkeri represented the deeply divergent sister taxon of all remaining nominal Chelodina species (Figs 1 and 2). Using coding sequences (CDS dataset; Fig. 2), the deeply divergent C. steindachneri and a clade comprising the holotype of C. oblonga plus a fresh sample of C. colliei represented the successive sister taxa of two crown clades including the remaining nominal Chelodina taxa. However, using the FULL dataset (Fig. 1), C. steindachneri clustered with moderate support with the clade containing the C. oblonga type and C. colliei. In any case, the sequences of the holotype of C. oblonga and the fresh sample of C. colliei were nearly identical, and together distinct.

One of the two crown clades of Chelodina showed substantial genetic structure and contained as successive sister taxa the holotype of C. kuchlingi, a fresh sample of C. oblonga sensu Thomson24 (Finnis River, Northern Territory) and a terminal clade comprised of the holotype of C. siebenrocki plus a GenBank mitogenome of C. oblonga sensu Thomson24 of unknown provenance. Both the holotype of C. kuchlingi and the C. oblonga sensu Thomson24 from the Finnis River were clearly distinct with long branches, whilst branch lengths for the holotype of C. siebenrocki, a nominal species described from New Guinea, and the GenBank mitogenome of C. oblonga sensu Thomson24 were only moderately differentiated. The other crown clade contained three clades with individual terminals having short branches. One terminal clade contained the holotype of Testudo longicollis plus a fresh sample of C. expansa from the Murray-Darling drainage. The second terminal clade consisted of taxa from New Guinea, with C. pritchardi being sister to the holotype of C. gunaleni plus a virtually undifferentiated clade containing the lectotype of C. novaeguineae and the holotype and a paratype of C. reimanni. The third terminal clade comprised taxa from Australia and the islands of Roti and Timor. The paratype of C. mccordi and a fresh sample of the same species were virtually undifferentiated from the holotype of C. mccordi roteensis. The sequences for the holotypes of C. mccordi timorlestensis and C. timorensis were identical and sister to the aforementioned clade containing among others the paratype of C. mccordi. The remaining sequences from the same terminal clade corresponded to Australian taxa, constituting a weakly supported clade with C. burrungandjii being sister to a well-supported clade embracing C. canni as sister taxon of the weakly differentiated sequences from a C. expansa from the Dawson River, Fitzroy, Queensland (GenBank accession number KY705230) and a C. longicollis from the Australian Capital Territory47 (KJ713173).

Within the short-necked clade, a moderately supported clade embracing Rheodytes leukops, Elusor macrurus, and Myuchelys purvisi was sister to the remaining taxa. Elusor macrurus and M. purvisi were in this clade as maximally supported sister taxa, rendering Myuchelys polyphyletic. Among the remaining taxa, the species of the genus Elseya were monophyletic and sister to two other clades, one containing the species of Emydura and the other those of Myuchelys, except M. purvisi. With respect to the studied type specimens, the sequence of the holotype of Elseya intermedia was identical with a sequence of El. dentata from the Victoria River, Northern Territory (Elden258), and the sequence of the holotype of Phrynops bellii was identical to that of a fresh sample of the same species (M. bellii) from the Gwydir River, Murray-Darling Basin, New South Wales. Within Emydura, the sequence of the lectotype of Hydraspis victoriae was identical to a sequence of a fresh sample of Em. macquarii from the Murray River, Murray-Darling Basin, whilst the paralectotype of Hydraspis victoriae clustered with maximum support with the holotype of Hydraspis australis. Both types of Hydraspis victoriae did not cluster with a fresh sample identified with Em. victoriae. This fresh sample of Em. victoriae from the Daly River, Northern Territory, was placed together with a GenBank sequence of Em. subglobosa (KC692462) of unknown provenance and Em. tanybaraga from the Mitchell River, Queensland, in a maximally supported clade which was sister to a clade comprising a fresh sample of Em. subglobosa from Roper River, Northern Territory, and the sequence of the holotype of Euchelymys subglobosa. The latter two sequences clustered with maximum support, but their genetic divergence resembled those between El. branderhorsti and El. flaviventralis and exceeded the divergence between Em. tanybaraga and a fresh sample of Em. victoriae from the Daly River, Northern Territory.

Discussion

Our analysis of mitogenomes, including those of key type specimens, resolves a number of taxonomic and nomenclatural controversies. Perhaps the most significant is that of the status of Chelodina oblonga Gray, 1841, which has been controversial for 130 years48. The near-identity of the mitogenomes of the holotype of C. oblonga and what is currently named C. colliei Gray, 1856 challenge the nomenclatural conclusions of Thomson24,48. Using morphological evidence, this author identified C. oblonga as conspecific with what was before C. rugosa Ogilby, 1890, rendering the latter name a junior synonym of C. oblonga, whilst for the southwestern species previously identified with C. oblonga the name C. colliei had to be reinstated. Considering this contorted nomenclatural history and how dubious the holotype of C. oblonga has become, with disagreement between molecular data (this study), collection data, and morphology24,48, we declare C. oblonga Gray, 1841 a nomen dubium. This delivers nomenclatural stability to this group of species, with C. colliei applying to the long-necked turtle confined to the southwest of Western Australia. For the species that was since Thomson48 identified with C. oblonga, the name C. rugosa Ogilby, 1890 has to be resurrected.

Within this species complex, C. rugosa Ogilby, 1890 and C. siebenrocki Werner, 1901 have been variously regarded as distinct species49,50,51,52 or the same53,54,55. Morphological evidence in support of their separation is scant. Burbidge et al.51 (p. 393) mention only ‘consistent, if minor, differences’ between the two as their basis for recognizing them as separate species. Rhodin & Mittermeier56 failed to reliably distinguish C. rugosa and C. siebenrocki following a morphological analysis, and chose to refer to them collectively as the C. rugosa complex. In the absence of any substantive diagnostic morphological differences and any fixed allozyme differences, Georges et al.57 synonymised C. siebenrocki with C. rugosa. The mitogenome of the holotype of C. siebenrocki is weakly differentiated (1.51%) from the mitogenome of a C. rugosa of unknown origin (GenBank HQ172157; Figs 1 and 2). However, their divergence is similar to that of other Chelodina species or subspecies (C. gunaleni vs. C. novaeguineae and C. reimanni: 1.37–1.41%; C. m. mccordi vs. C. m. timorensis as defined below: 1.01–1.04%; C. canni vs. the sister clade comprised of introgressed C. expansa and C. longicollis: 1.33–1.40%; Table S5). Another mitogenome of C. rugosa from the Finnis River, Northern Territory (sample Chrug313), is deeply divergent from both and differs by 5.53% and 5.71% uncorrected p distance from the holotype of C. siebenrocki and the GenBank mito-genome of C. rugosa, respectively, suggesting that more than one species is involved here. This is also supported by the previously reported deep divergence between two samples of C. rugosa from Queensland and the Northern Territory using 45 allozyme loci57. For the Northern Territory form the name Chelodina intergularis Fry, 1915 is available, if it should be considered to represent a separate species in the future.

The sister taxon of the clade comprising the mitogenomes of C. rugosa (= C. oblonga sensu Thomson) and C. siebenrocki is represented by the mitogenome of the holotype of C. kuchlingi Cann, 1997. This nominal species has been regarded variously as a valid taxon9,14,58 or not10,59 because it was described from a single specimen of uncertain provenance, without a scientifically defensible diagnosis or description. No living specimens of C. kuchlingi have been found since its description, despite extensive searches. With respect to uncorrected p distances, the mitogenome of the C. kuchlingi type differs from that of the most similar species, a C. rugosa from the Finnis River, Northern Territory (sample Chrug313), approximately 660 km east of the type locality of C. kuchlingi, by 3.78% and from other Chelodina species, by 5.72–10.37% (Table S5). Considering only the COI gene, we found that C. kuchlingi differs from C. rugosa and C. burrungandjii by between 4.4% and 6.4%. This is in contrast to a previous report, without supporting data or a clear indication of the specimens sequenced, that C. kuchlingi differs by 14–18% in mitochondrial COI sequence from other species of northern snake-necked turtles (C. oblonga = C. rugosa and C. burrungandjii)58. Nevertheless, our data support C. kuchlingi as a valid species. However, the stated type locality of Kalumbaru60 is in doubt10, and we were unable to link the taxon to any population of Chelodina. Locating populations of this species is thus a high priority.

Our analysis also resolves the confusion over taxa associated with the name Chelodina mccordi Rhodin, 1994. Two taxa have been recognised from the island of Roti, namely Chelodina mccordi mccordi Rhodin, 1994 from the western side of the island and Chelodina mccordi roteensis McCord, Joseph-Ouni & Hagen, 2007 from the eastern side9. The mitogenomes of the holotype of C. m. roteensis and a topotypic paratype of C. mccordi (and of a non-type sample of C. mccordi from Roti) are identical. We therefore formally place C. m. roteensis McCord, Joseph-Ouni & Hagen, 2007 in the synonymy of C. m. mccordi Rhodin, 1994.

The mitogenomes of the turtles from Roti island are slightly distinct from and sister to those of the holotypes of C. m. timorensis McCord, Joseph-Ouni & Hagen, 2007 and C. m. timorlestensis Kuchling, Rhodin, Ibarrondo & Trainor, 2007 from Timor Leste. The mitogenomes of the holotypes of C. m. timorensis and C. m. timorlestensis are identical, matching their current understanding as one and the same taxon9.

With respect to the Chelodina species from New Guinea, the mitogenome of C. pritchardi differs from that of other Chelodina species by uncorrected p distances between 3.1% (Chelodina novaeguineae and related taxa) and 11.04% (C. parkeri), supporting its distinctness. The mitogenomes of the holotype and paratype of Chelodina reimanni Philippen & Großmann, 1990, however, show negligible divergence from that of the lectotype of C. novaeguineae Boulenger, 1888 (0.2%). Using 45 allozyme loci, the two taxa were also found undifferentiated57. This suggests that the distinctive morphology of C. reimanni represents phenotypic plasticity, perhaps in response to a food source that stimulates macrocephaly. Macrocephaly is also known from other turtle species and thought to represent an adaptation to crushing hard-shelled food. Besides generally broad-headed species61, macrocephaly also occurs in some taxa only locally or as a sex-specific trait (Chelidae: Emydura australis, E. krefftii, E. tanybaraga, E. victoriae, E. subglobosa worrelli58; Emydidae: Emys orbicularis hellenica62; Graptemys barbouri, G. ernsti, G. gibbonsi, G. pearlensis, G. pulchra63,64; Geoemydidae: Mauremys reevesii61; Trionychidae: Apalone ferox65; for further examples, see Iverson et al.61), supporting that C. reimanni could be only a local variant of C. novaeguineae. Alternative explanations for the near-identity of their mitogenomes and the lack of differentiation in allozymes are mitochondrial introgression or recent origin of both taxa. We tentatively recognize C. novaeguineae and C. reimanni as distinct taxa pending further research using additional morphological data and nuclear markers applied across a more comprehensive geographical range of the species.

The status of C. gunaleni McCord & Joseph-Ouni, 2007 from New Guinea has also been controversial9,10,66,67, and Georges & Thomson10 placed C. gunaleni into the synonymy of C. novaeguineae. In our mitogenomic phylogeny, C. gunaleni is the sister taxon of C. novaeguineae/C. reimanni (Figs 1 and 2). The mitogenome of the holotype of C. gunaleni differs by uncorrected p distances of 1.37–1.41% from the mitogenomes of C. novaeguineae and C. reimanni (Table S5), supporting the proposed validity of C. gunaleni9.

For the short-necked species, we are able to support the identification of the holotype of Phrynops bellii Gray, 1844 of unknown provenance with the Myuchelys species from the Gwydir and Namoi Rivers of the Murray-Darling Basin, as suggested by Cann14. This author investigated the itineraries of potential collectors of the historical type specimen and concluded that it came from west of the Great Dividing Range, and could not represent Myuchelys latisternum to which it might otherwise have been assigned. Our mitogenome data complements this circumstantial evidence and confirms the identity of Myuchelys bellii (Gray, 1844).

Furthermore, we were able to confirm the synonymy of Elseya intermedia Gray, 1872 with Elseya dentata (Gray, 1863). The mitogenome of E. intermedia is virtually identical to a fresh sample of E. dentata from the type locality of Victoria River, Northern Territory (Elden258), supporting the view that E. intermedia Gray, 1872 is a junior synonym of Chelymys dentata Gray, 18639,10,52.

The mitogenomes of the other type specimens of short-necked chelids are relevant to some complicated taxonomic issues. In a much-debated privately published document (see the review in Iverson et al.68), Wells & Wellington69 designated in 1985 a lectotype (BMNH 1947.3.5.95) for Hydraspis victoriae Gray, 1842, assuming that the original description of this species70 was founded on two specimens. Using morphology, Iverson et al.68 concluded that these two putative type specimens represent two distinct species. The name-bearing lectotype was identified as the species currently called Emydura macquarii, rendering Hydraspis victoriae Gray, 1842 a junior synonym of Chelys (Hydraspis) macquarii Gray, 1830, whilst the paralectotype of H. victoriae (BMNH 1947.3.5.96) is an Em. victoriae following the intent of its describer Gray70. Our results support that the lectotype is an Em. macquarii. The mitogenome of the lectotype differs from that of an Em. macquarii from the Murray River, New South Wales (Emmac119), by only three mutations (0.02% uncorrected p distance; Table S5). The mitogenome of the paralectotype of H. victoriae is distinct and clusters with that of the holotype of H. australis Gray, 1841, with 0.68% uncorrected p distance between both. These two mitogenomes together are sister to Em. macquarii, represented by the individual from the Murray River and the lectotype of H. victoriae (2.31–2.35%; Table S5), providing evidence against their identity. This intricate situation is further complicated by the occurrence of a third mitogenome from a turtle identified with Em. victoriae from the Daly River, Northern Territory (Emvic245) in another deeply divergent clade, clustering together with the mitogenomes of Em. subglobosa and Em. tanybaraga (Figs 1 and 2). This suggests that the turtles from the Daly River identified with Em. victoriae represent another species, as supported by previously published allozyme evidence and distinct coloration71.

The nomenclatural situation is further confused by the fact that Cann & Sadlier58 concluded recently that the superficial description of Em. victoriae (Gray, 1842) was based on only one individual (in their view BMNH 1947.3.5.96), so that the type status of one of the two currently recognized type specimens is challenged. Gray’s description of Hydraspis victoriae70 gave no indication how many specimens were available and his intention was clearly to describe a new species from the Victoria River, Northern Territory. As such, the specimen selected by Wells & Wellington69 as lectotype (BMNH 1947.3.5.95), most likely from the Murray River in southern Australia, cannot be considered a type specimen of Hydraspis victoriae even though it has been regarded as such since the late 19th century72. In addition, it was associated with erroneous locality data (“Victoria River, N. W. Australia”) ever since this was stated in Boulenger’s Catalogue of the Chelonians, Rynchocephalians, and Crocodiles in the British Museum (Natural History) in 188972. However, the handwritten question mark after the locality in Boulenger’s private copy of the Catalogue in the Natural History Museum, London, shows that Boulenger was in doubt about the provenance of this specimen. That BMNH 1947.3.5.95 is not a type of Hydraspis victoriae is further corroborated by the observation that Gray73 (p. 42) earlier explicitly mentioned only one specimen in his Catalogue of the Tortoises, Crocodiles, and Amphibaenians in the Collection of the British Museum of 1844, a shell, identified with “H. Victoriae, Gray” from the “Victoria River, N. W. coast of Australia”. This is clear evidence that the original description of Hydraspis victoriae Gray, 1842 was based on only one specimen (BMNH 1947.3.5.96), which has to be regarded as the holotype, making the previous designation of BMNH 1947.3.5.95 as lectotype69 invalid (article 74.2 of the International Code of Zoological Nomenclature74). Consequently, the name Emydura victoriae (Gray, 1842) is unambiguously validated for the red-faced Emydura species from the Victoria River, Northern Territory.

Hydraspis australis Gray, 1841 is another much debated taxon, currently treated as a junior synonym of Em. macquarii (Gray, 1830)10,52 or as a nomen dubium9. Previously, the name Em. australis has also been used for certain Emydura populations from northern Australia14. The differentiation of the mitogenome of the holotype of H. australis suggests that it is distinct from E. macquarii and may thus represent a valid species. Unfortunately, the type locality of H. australis is unknown75, even though it has been suggested to originate from “Western Australia”10,52 (which at the time included much of what we now call the Northern Territory) or the Macquarie River76. This situation requires wider sampling of fresh material to clarify the distribution of this species.

Besides these nomenclatural and taxonomic aspects, our sampling of mitogenomes of type specimens and fresh material allow some additional insights. Chelid turtles represent an iconic part of the extant fauna of South America and Australasia and are a prime example of a group of animals of Gondwana origin77. The topology of our phylogenies (Figs 1 and 2) corresponds to expectations from previous studies using less data or less taxa26,78,79,80. The mitogenomes of Australasian chelids support four ancient lineages, (1) Pseudemydura umbrina, (2) snake-necked and long-necked turtles of the genus Chelodina, (3) a clade comprised of the genera Elseya, Myuchelys (exclusive of M. purvisi) and Emydura, and (4) a clade containing M. purvisi and the monotypic genera Elusor and Rheodytes.

The mitogenome of Pseudemydura umbrina has it as the sister taxon to the remaining Australasian taxa, as recently revealed by a limited dataset of mitogenomes, including P. umbrina26. The mitogenomes of Chelodina species form a well-supported deep clade within the Australasian Chelidae. Within this genus, morphological and allozyme variation has been used to establish three major clades10, named as the subgenera (1) Chelodina, containing the long-necked species C. canni, C. longicollis, C. mccordi, C. novaeguineae (with C. gunaleni as junior synonym10), C. pritchardi, C. reimanni, and C. steindachneri; (2) Macrochelodina, corresponding to the snake-necked species C. burrungandjii, C. expansa, C. parkeri, and C. rugosa (the latter species thought to be synonymous with C. kuchlingi and C. siebenrocki10); and (3) the monotypic Macrodiremys for the snake-necked C. colliei.

Our mitogenome analysis conflicts with this arrangement in several respects. First, the mitochondrial genome of C. parkeri is sister to those of all remaining Chelodina species. This placement of C. parkeri is unexpected because it conflicts both with morphological groupings within Chelodina10,51,55,56 and allozyme evidence57, which both place C. parkeri in a clade also comprising C. burrungandjii, C. expansa, and C. rugosa81. Our mitogenomic phylogeny implies that the snake-necked condition is ancestral and retained by C. burrungandjii, C. colliei, C. expansa, C. parkeri, C. rugosa, and the newly recognized species C. kuchlingi, and secondarily reduced in the long-necked species C. canni, C. longicollis, the C. novaeguineae complex, and C. steindachneri. Alternatively, the snake-necked character state must have arisen at least three times independently (in C. parkeri, C. colliei, and the clade comprising C. burrungandjii, C. expansa, C. kuchlingi, and C. rugosa), leading to the phylogenetic interdigitation of the snake-necked and long-necked species, rendering the Macrochelodina subgenus polyphyletic (Figs 1 and 2).

Another unexpected finding refers to C. expansa and C. longicollis, two species highly distinct in morphology14,55,58 and allozyme profiles57. Two samples of each species yielded two highly distinct mitogenomes that occurred in two distinct phylogenetic positions. The mitogenome of the approximately 230-year-old holotype of Testudo longicollis is feebly differentiated from a C. expansa mitogenome from the Murray-Darling drainage (Chexp175). These two mitogenomes together are sister to a clade containing the mitogenomic sequences of several taxa from Australia and New Guinea, including several type specimens (Chelodina subgenus: C. canni, C. gunaleni, C. m. mccordi, C. m. roteensis, C. m. timorensis, C. m. timorlestensis, C. novaeguineae, C. pritchardi, C. reimanni; Macrochelodina subgenus: C. burrungandjii) and the virtually identical mitogenomes of a C. expansa (KY705230) from the Dawson River in Queensland and another previously published mitogenome sequence of C. longicollis from the Australian Capital Territory (KJ713173)47. This implies for C. expansa and C. longicollis multiple mitochondrial introgression events, a finding in line with the yet unpublished results of the PhD thesis of Hodges82. This situation also suggests that mitochondrial capture could have occurred in further Chelodina lineages. If this hypothesis is true, it could explain the polyphyly of the mitogenomes of the Chelodina subgenera. This is also supported by the observation of natural hybridization involving other Chelodina species (C. burrungandjii × C. canni, C. burrungandjii × C. rugosa, C. canni × C. longicollis, C. canni × C. rugosa)10,15,57,83, leading in the Arnhem Land region to widespread mitochondrial introgression of C. burrungandjii with C. rugosa haplotypes83.

Another deeply divergent clade identified by our analysis comprises the species of Elseya, Emydura and Myuchelys (excluding Myuchelys purvisi). The three major clades of Elseya, Emydura and Myuchelys are consistent with the findings of prior studies71,84. The Queensland east coast Elseya albagula is the sister taxon to the Elseya from northern Australia; within that northern clade El. branderhorsti and El. flaviventralis cluster together, a reflection of the close historical relationship between Australia and the island of New Guinea. Within the Myuchelys clade (excluding M. purvisi), M. georgesi is sister to a clade represented by M. latisternum east of the Great Dividing Range and M. bellii west of the range. Our data support two clades within Emydura. One northern clade contains Emydura subglobosa as sister taxon to a clade comprising the Em. victoriae (Emvic245) from the Daly River, Northern Territory, and Em. tanybaraga, which is consistent with earlier findings based on allozymes71,84. Another mitogenome, identified as “Emydura subglobosa”, was downloaded from GenBank (KC692462) and seems to originate from a trade turtle without locality data. It is virtually identical to our mitogenome of Em. tanybaraga. Since Em. subglobosa and Em. tanybaraga are morphologically similar, a misidentification seems likely. The second clade within Emydura includes the holotype of Em. australis and the holotype of Em. victoriae (previously misidentified as paralectotype) as one clade, and the southern Em. macquarii, represented by the mitogenomes of a fresh sample (Emmac119, Murray River, New South Wales) and the mitogenome of the historical museum specimen that was previously misidentified as the lectotype of Hydraspis victoriae as another clade (see discussion of species identification above).

The paraphyly of the genus Myuchelys supported by our data is consistent with the findings of past studies using mitochondrial data85,86. Using one nuclear and two mitochondrial markers, Le et al.86 concluded that Myuchelys purvisi, Elusor macrurus and Rheodytes leukops constitute the successive sister taxa of all other short-necked Australasian chelids (Pseudemydura umbrina was not studied), rendering Myuchelys polyphyletic. Based on this topology, Le et al.86 removed M. purvisi from Myuchelys and placed it in the newly described genus Flaviemys. Using one mitochondrial and 13 nuclear loci, Spinks et al.87 found conflicting evidence from the two marker systems in that they revealed for the mitochondrial COI gene the same topology that we did. However, based on the nuclear loci M. purvisi clustered with high support among the other studied Myuchelys species, and Spinks et al.87 therefore relegated Flaviemys Le et al.86 into the synonymy of Myuchelys Thomson & Georges, 2009.

We suggest that the conflicting topologies of the well supported nuclear and mitochondrial trees reflect ancient mitochondrial capture, and that M. purvisi carries the mitochondrial heritage of an extinct lineage related to El. macrurus and R. leukops. If this hypothesis is correct, M. purvisi could represent the oldest case of mitochondrial capture. Fossils identifiable as Myuchelys date back to the Albian (Lower Cretaceous, 113–100.5 Ma)88, and fossils representing the lineage of M. purvisi date back to the upper Eocene or Oligocene (41–27 Ma)89, implying their long distinctness from the Elusor and Rheodytes lineages. Mitochondrial introgression, resulting in cytonuclear discordance, is widespread in animals90,91,92,93,94,95,96 and also known for a number of turtle species (Geoemydidae: Cyclemys, Malayemys97,98,99; Emydidae: Actinemys, Emys, Emydoidea, Graptemys100,101,102), among them is also the Chelodina genus (Chelidae; see above). However, mitochondrial capture, i.e. the complete replacement of the original mitochondrial genome with that of another species through introgressive hybridization, is much rarer. Cases have been described for insects103, freshwater fishes104,105,106, newts107, frogs108,109,110,111, turtles97,100,101,102, lizards112, snakes113, and bovids114,115,116,117, with the oldest case (12 Ma) referring to emydid turtles100.

In summary, we have resolved a number of important issues that have confused the taxonomy of this family in Australasia. We were able to assign the holotype of Phrynops bellii to populations of Myuchelys from the rivers of the Murray-Darling Basin draining west from Australia’s Great Dividing Range, confirming is previous identification based on circumstantial evidence inferred from the travels of the person who collected it14. We clarified the confusion over the name-bearing type of Emydura victoriae (Gray, 1842), and recognized the specimen previously misidentified as its paralectotype as the holotype. The deep divergence between the mitogenome of the holotype from a mitogenome of a fresh sample of Em. victoriae from the Daly River, Northern Territory, suggests together with differences in allozyme profiles and coloration71 that two distinct species are currently lumped together under the name Em. victoriae. The holotype of Emydura australis (Gray, 1841) remains of uncertain geographic provenance but is considered to represent a valid species. Chelodina kuchlingi Cann, 1997, which was described from a single specimen of uncertain provenance, is confirmed as distinct based on its mitogenome, and the recent assignment of the holotype of Chelodina oblonga Gray, 1841 to northern Australian populations is brought into question, requiring the resurrection of C. rugosa Ogilby, 1890 for those populations. However, the genetic divergences within the C. rugosa complex suggest the existence of multiple species. We identified only two taxa within C. mccordi Rhodin, 1994, at the level of subspecies, from the islands of Roti and Timor, respectively.

We have combined the mitogenomes of the studied types with those of fresh material to improve our understanding of the phylogenetic relationships of this morphologically conservative family of turtles, providing evidence for multiple old mitochondrial introgressions in chelid turtles. This study established the value of generating diagnostic sequences from type specimens of taxa with a confused and uncertain taxonomic and nomenclatural history. DNA sequencing of name-bearing type specimens is the gold standard for assigning extant populations to a named entity7 and enables the setting of clear and essential distinctions between newly discovered forms and those that have already been described.

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