- Research article
- Open Access
Molecular phylogenetics and evolutionary history of ariid catfishes revisited: a comprehensive sampling
© Betancur-R; licensee BioMed Central Ltd. 2009
- Received: 14 April 2009
- Accepted: 23 July 2009
- Published: 23 July 2009
Ariids or sea catfishes are one of the two otophysan fish families (out of about 67 families in four orders) that inhabit mainly marine and brackish waters (although some species occur strictly in fresh waters). The group includes over 150 species placed in ~29 genera and two subfamilies (Galeichthyinae and Ariinae). Despite their global distribution, ariids are largely restricted to the continental shelves due in part to their specialized reproductive behavior (i.e., oral incubation). Thus, among marine fishes, ariids offer an excellent opportunity for inferring historical biogeographic scenarios. Phylogenetic hypotheses available for ariids have focused on restricted geographic areas and comprehensive phylogenies are still missing. This study inferred phylogenetic hypotheses for 123 ariid species in 28 genera from different biogeographic provinces using both mitochondrial and nuclear sequences (up to ~4 kb).
While the topologies obtained support the monophyly of basal groups, up to ten genera validated in previous morphological studies were incongruent with the molecular topologies. New World ariines were recovered as paraphyletic and Old World ariines were grouped into a well-supported clade that was further divided into subclades mainly restricted to major Gondwanan landmasses. A general area cladogram derived from the area cladograms of ariines and three other fish groups was largely congruent with the geological area cladogram of Gondwana. Nonetheless, molecular clock estimations provided variable results on the timing of ariine diversification (~105-41 mya).
This study provides the most comprehensive phylogeny of sea catfishes to date and highlights the need for re-assessment of their classification. While from a topological standpoint the evolutionary history of ariines is mostly congruent with vicariance associated with the sequence of events during Gondwanan fragmentation, ambiguous divergence time estimations hinders assessing the vicariant hypothesis on a temporal framework. Further examination of ariid fossils might provide the basis for more accurate inferences on the timing of ariine diversification.
- Markov Chain Monte Carlo
- Maximum Parsimony
- Biogeographic Province
- Morphological Phylogeny
- Mitochondrial Dataset
The catfish order Siluriformes is a very diverse natural group that occurs primarily in freshwater. Catfishes are widespread and their distribution encompasses all continents, even Antarctica, as evidenced by Eocene-Oligocene fossils . The order includes 36 extant families and over 3000 valid species plus an estimated ~1500 undescribed species [2, 3]. Several morphological and molecular studies have addressed the relationships among catfish families [e.g., [4–6]] and recent evidence indicates that large basal clades are restricted to particular continental masses, suggesting a long history of intercontinental isolation . Thus, catfishes offer an exceptional opportunity for studying evolutionary and biogeographic trends. The fossil record of Siluriformes is relatively well represented and includes material from every continent . Although the earliest fossils date back to the Late Campanian-Early Maastrichtian (ca. 68-73 mya), molecular clocks predict a much older origin for Siluriformes (i.e., 175-130 mya [8–10]).
Members of the Ariidae exhibit a specialized reproductive mode: male mouthbrooding of eggs and embryos. This condition is absent in nearly all other catfishes, the sole exception being the biparental mouthbrooding claroteid Phyllonemus typus . Oral incubation means ariids have limited dispersal capabilities and subsequent high level of species endemism, which has ultimately resulted in continentally restricted distributions. In fact, ariids are absent from the Pacific plate , the nonmarginal portion of the Antilles, and other oceanic islands of recent volcanic origin . Restriction of most species to the continental shelves make ariids an exceptional marine fish group to infer historical biogeography scenarios (although see  for evidence of recent transoceanic dispersal in Galeichthys). Such studies require a conceptual framework derived from robust phylogenetic hypotheses.
Recent interfamilial phylogenies based on morphological [15, 16] and molecular  data have placed the Malagasy family Anchariidae as sister to the Ariidae and both families are ascribed in the superfamily Arioidea within the suborder Siluroidei . The monophyly of the Ariidae has not been seriously questioned and is strongly supported on both molecular and morphological grounds [6, 15, 17]. The group is divided into two subfamilies, the monogeneric Galeichthyinae (four species) and the Ariinae (remaining taxa) . Although the basal arioid clades are well defined, much controversy has arisen regarding the phylogeny and classification of ariid taxa, particularly within the diverse Ariinae.
This study expands previous molecular phylogenies on New World ariids and galeichthyines using mitochondrial sequences (cytochrome b, ATP synthase 8/6, 12S, and 16S; ~3 kb) and a nuclear marker (rag2, ~1 kb) to cover a wide spectrum of taxa from different biogeographic provinces. In addition to the 63 ariid species examined previously [14, 19], new molecular data was obtained for 60 other species. These data were utilized for three main purposes: (1) hypothesize ariid relationships via maximum parsimony (MP), maximum likelihood (ML), and Bayesian inference (BI) reconstruction criteria; (2) discuss morphological phylogenies and current classifications in the light of molecular phylogenies; and (3) infer historical biogeography scenarios for the Ariinae using cladistic and chronological methods. This study provides the most inclusive phylogeny of ariid taxa to date and a resource for future classifications and other comparative studies in the family.
Partial ribosomal 12S and 16S sequences ranged in size from 385 to 394 bp and 556 to 571 bp, with final alignment lengths of 406 and 595 bp, respectively. In the final alignments, 18 sites of 12S and 54 sites of 16S were excluded due to ambiguous positional homology. The mitochondrial dataset assembled included 129 terminal taxa (124 arioid species including one anchariid, four galeichthyines, and 119 ariines) and 2866 sites. The dataset had missing data for Notarius luniscutis in ATPase 8/6 (due to amplification failure) and for Cathorops manglarensis (65 bp at 3' end) and N. lentiginosus (35 bp at 3' end) in 16S (due to polymerase slippage producing noisy sequences). Many other taxa also had missing data on sequence ends due to noisy chromatogram reads. Considering only arioid taxa, the mitochondrial alignment contained 1273 (44.4%) variable sites and 1097 (38.3%) parsimony-informative sites, respectively.
The nuclear rag2 gene has been shown to have low variability within the Ariidae , thus nuclear sequences were obtained only from major lineages (as indicated by the mitochondrial topologies) representing all biogeographic provinces and sampled genera (73 species). Due to amplicon-length variation from different primer combinations or noisy chromatogram endings, in the nuclear rag2 alignment not all ingroup taxa had the same sequence length, varying from 837 to 978 bp; outgroups had 720 bp [obtained from [6, 23]]. No insertions or deletions were observed in the rag2 dataset. The number of variable and parsimony-informative sites for the ingroup in the rag2 dataset were 174 (17.8%) and 67 (6.9%), respectively. In addition to the mitochondrial and nuclear partitions, a combined dataset including 73 common taxa was assembled (73 species, 3844 sites, 1525 variable sites, 1157 parsimony-informative sites).
Summary of initial conditions and results obtained in phylogenetic reconstructions and model testing.
129 taxa, 2866 bp
73 taxa, 978 bp
73 taxa, 3844 bp
1000 (10 RA rep.)
1000 (10 RA rep.)
Optimal trees retained
>5 × 104
Optimal tree score (steps)
50% majority rule
90% majority rule
Initial model (ML and BI)
Akaike information criterion
Number of substitution rate parameters
ML – Garli
Automatic termination* (generations)
1 × 104
1 × 104
1 × 104
Optimal tree score (lnL)
ML – RAxML
Optimal tree score (lnL)
1 × 107
6 × 106
6 × 106
2.5 × 106
1.5 × 106
1.5 × 106
Post-burn-in trees (combined searches)
~2.15 × 105
~1.35 × 105
~1.35 × 105
Efective Sample Size (all parameters)
50% majority rule
50% majority rule
50% majority rule
Delimitations of New World genera [sensu ] were congruent with the mitochondrial topologies; however, seven Old Word genera [sensu ] were found to be non-monophyletic (Figure 3, colored taxa; see below). In general, the relationships among basal ariine taxa were poorly resolved or supported, with short internodes (Figure 3B). While New World taxa were not monophyletic in any of the analyses, Old World ariines were grouped into a well-supported clade (node I, Figure 3). The basal nodes linking some New World genera (e.g., Occidentarius, Genidens, Potamarius, Ariopsis, and Sciades) to the Old World clade were often incongruent among different reconstruction criteria and poorly supported (node E, Figure 3). Within the Old World clade, taxa were generally grouped into well-defined biogeographic assemblages (Figure 3, colored bars). Overall inshore species conform to major Gondwanan provinces (Africa, Madagascar, India-SE Asia, and Australia-New Guinea or Sahul). Delimitations and nodal supports for such groups were high, except for the India-SE Asia assemblage that was often recovered as non-monophyletic with the Madagascar species (Arius madagascariensis) nested within. Offshore taxa found widely distributed along Indo-West Pacific shelves fell into three categories: the genera Netuma (Indo-West Pacific 1) and Plicofollis (Indo-West Pacific 2), and Brustiarius proximus (Indo-West Pacific 3, nested within the Australia-New Guinea clade; Figure 3). Resolution among Old World biogeographic clades was poor, except for the sister-relationship between Australia-New Guinea and Plicofollis (node N, Figure 3), which was fully congruent and well supported.
The India-SE group comprised two well-supported basal clades, with one including 'Sciades' sagor, Cephalocassis melanochir, and Hemiarius stormii (node K, Figure 3) and other grouping the remaining taxa (node L, Figure 3). The latter clade was largely unresolved. The relationships within Netuma, Carlarius, and Plicofollis were entirely resolved with high nodal support. There was poor resolution within the Australia-New Guinea assemblage (node O, Figure 3), except for the following well supported-clades: Brustiarius proximus + Amissidens hainesi (node P, Figure 3); Neoarius (in part; node Q, Figure 3); node R (Figure 3): node S (Potamosilurus, in part) + node T (Cinetodus carinatus, ('Sciades' utarus, (B. nox, B. solidus))); Pachyula crassilabris + Doiichthys novaeguineae + Nedystoma dayi (node V, Figure 3); and Cochlefelis (in part; node W, Figure 3).
The congruences between methods and data partitions (mitochondrial, nuclear, and combined) are summarized in Additional file 2. There was strong phylogenetic signal in the mitochondrial dataset, often yielding well-resolved and well-supported nodes. The weak signal and the small number of characters in the nuclear rag2 dataset (67 parsimony-informative sites) resulted in the greatest number of incongruent nodes (Additional file 2). Although using a more reduced taxon-sampling scheme, the combined partition yielded highly congruent topologies as compared to the mitochondrial topologies. The major difference is that the combined scheme recovered the India-SE Asia group as monophyletic in all topologies (only MP and ML-Garli in the mitochondrial partition), but failed to place the Madagascar species sister to the India-SE Asia clade. Incongruence between mitochondrial and nuclear datasets may be alternatively due to gene-tree/species-tree conflicts [35, 36]. Thus, given this situation, further exploration of ariid phylogeny should emphasize the inclusion of additional, independent nuclear markers.
The lack of resolution and short internodes evidenced among basal ariine lineages is consistent with the reconstructions conducted on the mitochondrial, nuclear, and combined partitions. Given that mitochondrial and nuclear markers contain different levels of signal , this pattern may be the result of rapid ariine radiations; however, further analyses are required to test this hypothesis [see ].
Morphological hypotheses, classifications, and alpha taxonomy
Incongruence between phylogeny and classifications derived from morphological studies and the molecular evidence.
# of taxa in constrained clade
48 (34 constrained nodes)
Marceniuk and Menezes (2007)
Arius excluding A. madagascariensis
Conflicts in phylogenetic hypotheses also have profound implications on the classification. Despite their economic importance, the taxonomy of the Ariidae has for a long time remained in a chaotic state and is probably the most unresolved among catfish families . This has caused a vast nomenclatural instability with species commonly jumping from one genus to another. Even the three recent studies that have addressed the classification of ariids reveal considerable disagreement [15, 19, 21]. The results presented here also differ from previous classifications in several aspects.
Despite the more restricted taxon sampling, the previous classification of New World taxa based on combined molecular and morphological characters  is fully congruent with current topologies. This study also validates the status and confirms monophyly of the New World genus Genidens [not included in ]. The major conflicts concern the morphology-based taxonomies as ten genera recognized by Kailola  and nine by Marceniuk and Menezes  (Figure 3A) were not monophyletic in any of the reconstructions conducted on the mitochondrial partition (broadest taxon sampling). Furthermore, Templeton and SH tests constraining each non-monophyletic genus into the mitochondrial dataset identified strong departures from congruence in 16 (nine in ; seven in ) out of the 19 comparisons (Table 2). Similar results were also obtained on reconstructions performed on single-gene partitions (results not shown).
The genus Arius has been one of the major problems concerning ariid systematics. As traditionally recognized, Arius is the largest and most widespread genus in the family [e.g., [40, 41]]. All recent studies [15, 19, 21] concur that the genus includes considerably fewer species than was previously accepted (< 25) and, unlike prior classifications, no New World species are currently placed in Arius. Although Arius sensu Kailola was not recovered as monophyletic, it is restricted to the India-SE Asia province and the topology with enforced monophyly was not rejected by the mitochondrial data. Similarly, the monophyly of Arius sensu Marceniuk and Menezes is not rejected by the topological tests, but only if the Malagasy species (A. madagascariensis) is excluded (Table 2). From a phylogenetic standpoint, the present results also suggest that the genera Netuma and Sciades sensu Kailola and Brustiarius, Cochlefelis, Neoarius, and Potamosilurus sensu Marceniuk and Menezes each include only a few species incorrectly assigned to them.
In the light of the classification adopted for this study (see Materials and Methods), Notarius [sensu ], Cathorops, Arius, and Plicofollis are among the most species-rich genera in the family. Delimitation of the Neotropical Notarius sensu Marceniuk and Menezes is similar to that of Betancur-R. et al., except that Marceniuk and Menezes placed N. rugispinis and N. phrygiatus in their new genus Amphiarius, and N. luniscutis and N. quadriscutis in Aspistor. Validating Amphiarius and Aspistor would render Notarius paraphyletic (although in some analyses Aspistor was recovered as sister to all other Notarius; see Table 2). Aspistor was also recognized by Kailola but with a different circumscription, including seven species of Notarius sensu Betancur-R. plus Hemiarius hardenbergi (from Australia-New Guinea) and Occidentarius platypogon. The monophyly of Notarius sensu Marceniuk and Aspistor sensu Kailola are not supported by the molecular evidence (Table 2). A consensus solution for Notarius would be providing subgeneric assignments.
Molecular evidence also brings new perspectives at the alpha taxonomy level. While recent taxonomic check lists estimate that the number of valid ariid species range from 125 to 136 ([15, 21]; plus five more recent additions [42–44]), there are 53 species designated as inquirendae in the family (i.e., uncertain validity), the greatest number within the order Siluriformes [3, 39]. The major difficulties in undertaking a comprehensive taxonomic study of the Ariidae are the overall similarity in external morphology, the widespread distribution of the group coupled with the high degree of species endemism, and the poor representation of species diversity in museums [see also ]. Although estimating the total number of valid species is a challenging task, examination of wide variety of taxa on both mitochondrial and/or morphological grounds enabled identification of 20 putative undescribed/unrecognized species (referred as affinis or sp.; see Materials and Methods). The alpha taxonomy of the Ariidae is in need of revision.
Despite the recent efforts to clarify ariid taxonomy [15, 19, 21], these results show that it is still far from settled. This instability prevents an adequate management of the fisheries, making ariids a difficult group for conservational purposes. A total evidence approach based on combined morphological and molecular data would provide a suitable framework to redefine genera and to reassess the classification of the Ariidae. This issue will be addressed elsewhere.
Historical biogeography of the Ariinae
-The evolutionary history of ariines from a topological perspective
Presently, ariid distribution encompasses the New World, Africa, Madagascar, India-SE Asia, and the Sahul continent (Figure 1); however, as evidenced by the fossil record, the group also ranged into Europe until the Late Miocene. The current poor representation of catfishes in Europe has been attributed to extinctions caused by Pleistocene glaciations . While galeichthyines are restricted to subtropical waters in southern Africa and southwestern South America, sea catfishes owe their broad distribution to ariines. The disjunct biogeography of galeichthyines was recently addressed , thus this section focuses on ariines only.
In addition to the marked biogeographic associations, the Old World clade includes two subclades with widespread Indo-West Pacific distributions (Netuma and Plicofollis). Likewise, although Brustiarius proximus is nested within the Australia-New Guinea clade, its range extends into SE Asia (reported here for the first time). DIVA analyses indicate that the presence of B. proximus in SE Asia is most parsimoniously the result of dispersal from Australia-New Guinea. Thus, for component analyses, B. proximus is treated as a Sahul taxon. Inferring the biogeographic history of the widespread Netuma and Plicofollis is less straightforward because of ambiguous relationships among major Old World clades (Figs. 5B, C). According to DIVA optimizations on the mitochondrial dataset (broadest taxon sampling), the distribution of the common Plicofollis ancestor was either India-SE Asia or the composite India-SE Asia/Australia-New Guinea, whereas the ancestral distribution of Netuma was India-SE Asia/Australia-New Guinea.
Overall, the major differences between ariine (Figs. 5B, C) and geological area cladograms (Figure 5A) are the absence of ariine endemics from Sulawesi and the Seychelles and the lack of a close relationship between New World and African taxa. However, further analyses constraining the monophyly of the New World node G (Potamarius + Ariopsis + Sciades; see Figure 3) plus the African genus Carlarius, yielded scores similar to those obtained under unconstrained searches (SH test p value = 0.35; Templeton test p value = 0. 06–0.29). Similarly, while the placement of Australia-New Guinea, India-SE Asia, and Madagascar is variable among different reconstructions (Figs. 5B, C) and the predicted area relationship based on the Gondwanan model was not recovered (but see Garli ML reconstructions on the mitochondrial dataset; Additional file 2), additional analyses enforcing the Australia-New Guinea + (India-SE Asia + Madagascar) topology are not statistically rejected by the data (SH test p value = 0.472; Templeton test p value = 0.35–0.54; note that Netuma and Plicofollis were excluded from the analysis because their widespread distributions).
Component analyses on both MP and ML topologies derived identical general area cladograms (Figure 5E). The general fish area cladogram based on ariines, cichlids, aplocheiloid killifishes, and rainbowfishes (Figure 5E) is largely congruent with Sparks and Smith's  general area cladogram derived from the latter three groups only (Figure 5D) and the geological area cladogram (Figure 5A). The main difference is the truncated placement of Australia-New Guinea and India-SE Asia (Figure 5).
Although ariines are predominantly marine and therefore potentially capable of dispersing along contiguous intercontinental shelves (e.g., Netuma, Plicofollis, Brustiarius proximus), the fact that most taxa with limited dispersal capabilities were grouped into major Gondwanan clades and that relationships among these clades largely coincide (or at least are not significantly incongruent) with the geological history of the super continent, suggest vicariance via continental drift. While restricted distributions are the generalized condition within the Ariinae, widespread Indo-West Pacific taxa are derived from three independent acquisitions (Figure 3). If dispersal is historically the major force driving ariine biogeography, no provincial associations would be observed. As pointed out by Sparks and Smith  for cichlids, a close relationship between African and Malagasy taxa across the Mozambique canal is expected under a dispersalist model. However, the reconstructions presented here offer no evidence for Afro-Malagasy clades (although the two ariine species from Eastern Africa were not examined). Similarly, the sharp faunal division across Wallace's line (dividing SE-Asia and Australia-New Guinea plates) of most (i.e., non-widespread) ariine taxa disfavors dispersal acting as a homogenizing force. The collision of the India subcontinent into Asia 43 mya [50, 51] permitted faunal dispersal to SE Asia but not to the Australia-New Guinea plate due to deep oceanic barriers preventing faunal exchange across Wallace's line (except for the three Indo-Pacific taxa found in SE Asia and Australia-New Guinea). Remarkably, with the exception being the basal node linking New and Old World ariines (e.g., node E, Figure 3), the topologies do not show any transpacific or transatlantic nested clades within the Ariinae, supporting the idea that sea catfishes have limited transoceanic dispersal capability (but see  for evidence of recent dispersal from Africa to South America in the Galeichthyinae). As Sparks and Smith  argued, not only freshwater fishes in the primary division but also continentally restricted marine groups may be of great value for inferring ancient land connections.
The presence of ariines in non-Gondwanan areas such as Mesoamerica/North America and Europe (until Late Miocene) was probably the result of contiguous intercontinental marine dispersal from South America and perhaps Africa, respectively. In support for this scenario, DIVA analyses derived from the mitochondrial dataset (broadest taxon sampling) indicates South America as center of origin for New World taxa. Given that extant ariids are absent from Europe (but see records of the African Carlarius parkii in the Mediterranean ) further morphological studies including European fossils are required to test dispersal into this continent.
-The timing of ariine diversification in the context of Gondwanan vicariance
Recent studies have shown a variety of floral and faunal taxa whose disjunct distributions in the southern hemisphere, previously associated with Gondwanan vicariance, likely represent instances of transoceanic dispersal. Particularly, molecular dating techniques have revealed divergence times that are too young to be explained by continental-drift vicariance. Remarkable examples of recent transoceanic dispersal include geckos, monkeys, lemurs, carnivores, chameleons, frogs, insects, and several angiosperm families, among others [reviewed in ]. Contemporary advocates of dispersal even argue that vicariance should be revaluated as the most likely a priori assumption in biogeography [e.g., [46, 47]]. Accordingly, it seems appropriate to test the Gondwanan hypothesis of ariine diversification in a chronological framework.
The final separation of South America and Africa is dated to be as recent as 105 mya [53, 54], Madagascar and India separated at about 95-84 mya [51, 55, 56], and Australia and Antarctica initiated rifting 95 mya but remained connected until at least 35 mya . While the temporal context for the separation of India-Madagascar from the major Gondwanan landmass is more controversial [56, 58], it has been suggested that the Kerguelen Plateau served as a corridor allowing exchange of terrestrial and freshwater faunas between India-Madagascar and Australia via Antarctica until about 80 mya [48, 51, 58]. Before the Eocene, Antarctica had a temperate climate and included fish fauna found at lower latitudes today , such as catfishes reported from the Eocene/Oligocene boundary . Likewise, after the fragmentation of Gondwana, shallow marine connections between major landmasses might have remained open until ~80 mya (e.g., Africa and South America at 84 mya ) or later permitting exchange of continentally-restricted marine taxa such as ariines.
Under the Gondwanan model a Mesozoic origin of major ariine clades is predicted. Previous studies addressing the timing of catfish diversification provide no support for this scenario. Lundberg et al.  inferred nodal ages for siluriform families using nuclear rag1 and rag2 sequences and seven fossil calibration points via Bayesian relaxed clocks (BRC) and penalized likelihood analyses. Their divergence time estimation for arioids and ariines is ~73 my and ~20 my, respectively [: Fig. 2]. It is remarkable, however, that Lundberg et al. arbitrarily selected 144 my (informed by the fossil record of actinopterygians) as the maximum age constraint for the split of gymnotiforms and siluriforms. While addressing the timing of galeichthyine intercontinental disjunction, Betancur-R. and Armbruster  inferred 94-74 my (95% credibility interval 104-69 my) for the arioid split and 40 my (95% credibility interval 59-29 my) for the ariine split based on mitochondrial sequences and three calibration points. Instead of fixing the root of the tree to an arbitrary age, they used minimum and maximum age constraints on a terminal node based on the rising of the Panama isthmus 3.1-2.8 mya. In order to provide more accurate estimates on the divergence time of basal nodes in the arioid tree, this study selected 18 calibration points on two deep osteichthyan nodes, six non-arioid catfish nodes, and five arioid nodes (Additional file 3).
Divergence time estimates for selected nodes.
Galeichthys peruvianus + G. ater/G. feliceps
Some New World + Old World
Old World Ariinae
Indo-Pacific Ariinae (split India, Madagascar, and Asutralia-N. Guinea)
While cross-validation procedures for the nine fossil-based nodes suggest no internal conflicts, several calibration points are outside the arioid tree and thus may not be much informative (Additional file 3). It is also noteworthy that, following the recommendations outlined in Lundberg et al. , minimum age constraints based on fossils were applied one node below the pertinent taxon (e.g., ariid fossils of Late Campanian-Early Maastrichtian were assigned to the split of ariids and anchariids). Although conservative, this procedure may have resulted in underestimated nodal ages (at least for UCLN dates). An alternative solution for improving accuracy on divergence time estimates of basal arioid nodes could come from assigning additional ariid fossils to particular subclades. However, such work requires an exhaustive morphological examination of both fossil and recent taxa. Among catfish families, ariids include the oldest and most abundant elements in the fossil record. Ariid fossils have been identified from bony (48 localities) and otolith (68 localities) remains  and the fragments are widespread, including records from North and South America, Europe, Asia, and Africa. The oldest ariid fossils date from the Late Campanian-Early Maastrichtian in North and South America. Old World fossil remains also include Maastrichtian otoliths assigned to the Ariidae, but the oldest bony elements are from the lowermost Eocene (Europe, Africa and Asia) [7, 64]. Considering that the stratigraphic record indicates that by the Early Maastrichtian (~70 mya) ariids were already widely distributed [see : Fig. seventeen part 2], the origin of the group might be older, implying a failure of preservation and/or detection of ancient fossils. If that is the case, a precise assignment of the oldest known specimens to particular ariid subclades might provide more accurate molecular clock estimations in support of the vicariant scenario.
This study utilized mitochondrial, nuclear, and combined (up to ~4 kb) sequence data to infer phylogenies for arioids based on the most comprehensive taxon sampling to date (124 species/entities). While the reconstructions support the monophyly of basal groups (Arioidea, Ariidae, Galeichthyinae, and Ariinae), up to ten ariine genera (out of 25–30) validated by previous morphological studies are incongruent with the molecular phylogenies. These results stress the need for re-assessment of ariid classification.
The topologies recovered New World ariines as paraphyletic and Old World species were grouped into a well-supported clade. In further disagreement with morphological hypotheses that follow no biogeographic patterns, the molecular phylogenies group inshore ariine species into well-defined clades restricted to particular Gondwanan provinces (New World [three to five basal clades], Africa, Madagascar, India-SE Asia, and Australia-New Guinea). The general area cladogram derived from the area cladograms of cichlids, aplocheiloid killifishes, rainbowfishes, and ariines is largely congruent with the temporal sequence of events during the fragmentation of Gondwana. Nonetheless, the results obtained using BRC and UCLN methods are too variable, which hinders drawing definitive conclusions on the timing of ariine diversification in the context of Gondwanan vicariance. Further examination of additional ariid fossils might provide better calibration points for more accurate molecular clock estimates.
Generic nomenclature for New World and Old World ariids follows Betancur-R. et al.  and Marceniuk and Menezes , respectively. The datasets included a total of 123 ariid species/entities (see below), representing 28 genera and the two subfamilies (Galeichthyinae and Ariinae; ~230 total individuals sequenced). Based on current check lists and classifications [19, 21], all but one ariid genus (Batrachocephalus) was examined and at least 37 species in 16 genera were not examined due to unavailability of tissue samples. The phylogenetic sampling includes ariid species from 26 countries and all major biogeographic provinces. One species of the sister family Anchariidae (Gogo arcuatus) was also included in the ingroup (Arioidea sensu ); three distantly-related catfish families were used as outgroups (Heptapteridae, Ictaluridae, and Auchenipteridae, listed in ). Additional outgroups were also selected for divergence time estimations (see below). Material examined is listed in Additional file 1. Institutional abbreviations are as listed at .
For several taxa, two or more individuals were sequenced for at least one gene region (mostly ATP synthase 8/6). As many as 15 species revealed significant morphological and/or molecular (>1.5% genetic divergence) differentiation among localities, suggesting that several potential undescribed/unrecognized species exist. In such cases, different entities were analyzed as separate terminals, referring the individuals collected close to the type locality (if known) as the nominal species and the allopatric entities as affinis (aff.). Undescribed or unidentified species were listed to the genus level (sp.), whereas dubious identifications were treated as confer (cf.). Old World species placed in Sciades by Marceniuk and Menezes  were referred as 'Sciades' (see Discussion).
DNA data and phylogenetic reconstructions
Targeted mitochondrial regions included partial cytochrome b (cyt b) and complete ATP synthase subunits 8 and 6 (ATPase 8/6) protein-coding genes, and partial 12S and 16S ribosomal genes. Nuclear evidence included partial recombination activating gene 2 (rag2). Laboratory protocols, PCR conditions, utilized primers, and sequence alignment procedures are as described in Betancur-R. et al. . Two additional rag2 primers were designed for several ariid taxa that failed to amplify using the combination MHRAG2-F1 and MHRAG2-R1 [19, 66]: rag2.Ari.F, 5'-GAGCCTCACAGTGAAAACCCYGAG-3'; rag2.Ari.R, 5'-CTCCCTCTCCATCACTGCTGTAC-3'. Different combinations of these four primers yielded successful amplifications in all cases.
Phylogenetic reconstructions were performed under MP, ML, and BI criteria. The initial conditions used for different analyses are summarized in Table 1. The MP reconstructions were conducted in PAUP* v. 4.0b10  via heuristic searches with random addition (RA) of sequences and tree-bisection-reconnection (TBR); clade support was evaluated using non-parametric bootstrapping with RA and TBR. For ML and BI, the best-fit models of sequence evolution were estimated using the Akaike information criterion (AIC) in ModelTest v. 3.7 . All analyses were run unpartitioned. The ML analyses were performed in the programs Garli v. 0.951/0.96  and RAxML v.7.04 . Garli searches were conducted using automatic termination (genthreshfortopoterm command). RAxML searches were run in the CIPRES portal v. 1.13  under default configurations. ML nodal support was evaluated in RAxML using the rapid bootstrapping algorithm with automatic estimation of runs. For both Garli and RAxML searches, several runs from random-starting seeds were performed to check convergence of likelihood scores. Model parameters were estimated simultaneously (i.e., unfixed). Remaining settings were left at their default values.
The BI analyses were performed in MrBayes v. 3.1.2  via Markov chain Monte Carlo (MCMC) iterations. The MCMC analyses were conducted in triplicate using four chains and sampling trees every 100 generations. Conservatively, 25% of the first trees sampled in each MCMC run were discarded as burn-in. Marginal probabilities of summary parameters, consensus phylograms, and posterior probabilities of nodes were estimated from the post-burn-in samples of the three independent runs combined (Table 1). To confirm that post-burn-in trees were sampled from the actual MCMC posterior distribution, marginal parameters (MrBayes log file) were analyzed using the Effective Sample Size (ESS) statistic in the program Tracer ; ESS greater than 200 suggests that MCMC searches were run long enough to accurately represent the posterior distribution .
Alternative hypotheses were compared to the molecular topologies using the parsimony-based nonparametric Templeton test and the likelihood-based Shimodaira-Hasegawa (SH) test  as implemented in PAUP*. Three major hypotheses were tested: (1) Kailola's  morphological phylogeny (Figure 2A), (2) recent generic classifications derived from anatomical data [15, 21], and (3) a Gondwanan vicariance model for ariines. A MP tree that represented a particular hypothesis was estimated using constrained tree searches in PAUP*. The constrained trees were compared to the unconstrained MP topologies using the Templeton test. Likewise, constrained and unconstrained topologies were estimated under ML in Garli and compared via SH tests (1000 replicates and RELL sampling). For ML comparisons, the best-fit model and parameters were selected using the AIC.
Ancestral areas were reconstructed via dispersal-vicariance analyses as implemented in the program DIVA v. 1.2 . DIVA analyses were performed for inferring: (1) 'center of origin' for New World ariines (unit areas coded as South America/southern Central America, Mesoamerica/North America, Old World); (2) ancestral distribution of basal ariine lineages and widespread Indo-Pacific taxa (unit areas coded as New World, Africa, Madagascar, India-SE Asia, Australia-New Guinea). The number of ancestral areas was restricted to two using the maxareas command. All DIVA analyses were run on MP and ML topologies.
An area cladogram was constructed by replacing the names of terminal taxa with their distributions. The area cladograms for the Ariinae were compared to those inferred by Sparks and Smith  for cichlids, aplocheiloid killifishes, and rainbowfishes (Melanotaenioidei). A general area cladogram based on the four fish groups was then derived and compared to the general area cladogram hypothesized by Sparks and Smith using the latter three groups only. To handle widespread taxa, redundant distributions, and missing areas, a component analysis [76–78] was performed in the program Component v. 2.0 [79, 80]. Component analyses were run using the nearest-neighbor interchanges algorithm by minimizing the number of leaves added. Host without associates (= missing areas) were treated as missing information. Widespread associates were dealt under assumption 2 (i.e., areas including widespread taxa have monophyletic, paraphyletic, or polyphyletic relationships [76–78, 81]) by arbitrarily removing all but one area from the distribution of each widespread taxon [79, 80]. The general fish area cladograms were further compared to the geological area cladogram of Gondwanan breakup (summarized by Sparks and Smith  based on Smith et al.  and Storey ).
Divergence time estimations
Relative rate tests based on likelihood were performed on eight clades with different nesting hierarchies using the software r8s v. 1.71 [82, 83]. Four out of the eight comparisons suggested significant departures from a clock-like behavior (p < 0.05). Thus, two different methods that do not assume a strict molecular clock were used for chronological estimations, BRC as implemented in Multidivtime  and UCLN as implemented in Beast v. 1.48 [73, 85]. BRC analyses were run unpartitioned with detailed procedures outlined in Betancur-R. and Armbruster . The initial tree was estimated using ML (Garli) on combined protein-coding sequences (mitochondrial cyt b and ATPase 8/6, and nuclear rag2). In addition to the combined dataset, based on the recommendations outlined in Hurley et al. , divergence times were also estimated excluding the entire ATPase 8 fragment as well as third codon positions of cyt b and ATPase 6 to reduce the effect of saturated mitochondrial sequences [see also ]. Eighteen calibration points on two deep osteichthyan nodes, six non-arioid catfish nodes, and five arioid nodes were set as maximum (six points only) and minimum age constraints based on median fossil ages (see Additional file 3; material examined is listed in Additional file 1 [after [7, 10, 14, 33, 61, 86, 88–93]]). To assess internal consistency among calibration points, fossil-based cross-validation procedures were performed in r8s under penalized likelihood (PL) using truncated Newton algorithm and fossilconstrained command . Priors for the BRC analyses were calibrated as follows: rttm, rttmsd, and bigtime parameters were set to 45.0 (= 450 my; estimated divergence time between sarcopterygians and actinopterygians [61, 88]); rtrate and rtratesd parameters were both set to the mean value for the total evolution of all branches from the root to the tip of the tree divided by rttm (rtrate and rtratesd = 0.0468, combined dataset; rtrate and rtratesd = 0.0603, reduced dataset). Other priors were set to their default values and/or as specified in Betancur-R. and Armbruster .
For UCLN analyses, the initial Beast file was generated in BEAUti . The substitution model was GTR+I+Γ (as selected by AIC) with base frequencies estimated empirically, using two data partitions (first and second codon positions combined and third codon positions) for the complete dataset and three partitions (separate codon positions) for the reduced dataset. All parameters were unlinked and mean substitution rate was unfixed. A starting chronogram that replaced the UPGMA default tree and satisfied all UCLN priors was generated under PL in r8s. The tree prior parameter selected was Yule process, which assumes a constant speciation rate per linage and is more appropriate for species-level phylogenies . Calibration nodes were constrained using lognormal-distribution priors whenever there was confidence that fossils are close in time to cladogenesis (i.e., the stratigraphic record is fairly complete ; e.g., Osteichthyes and Actinoperi [61, 86, 88, 89]). As inferred by molecular clock analyses, the origin of siluriforms (i.e., 175-130 mya [8–10]) is much older than predicted by the oldest fossil (ca. 68-73 mya), suggesting a gap in the stratigraphic record. Thus, catfish nodes were constrained under uniform-distributions (Additional file 3). Tree root was set to 450 using uniform distribution (similar to bigtime parameter in BRC). Other priors and operators were set to their default values. The MCMC analyses were run in duplicate for 3 × 107 generations, sampling trees every 1000 generations. The MCMC log files were combined in Tracer to summarize posterior divergence times with 95% highest posterior density limits; ESS values greater than 200 were reached for all marginal parameters after discarding 20% of the first trees as burn-in.
This research was funded by the All Catfish Species Inventory (National Science Foundation DEB-0315963) and DeepFin Student Exchange Program. I am indebted to many colleagues that collaborated in several ways. Tissue samples and curatorial assistance were provided by H.H. Ng, M.H. Sabaj, R.G. Reina, M. Hardman, G. Allen, D. Werneke, H. Larson, C. Oliveira, M. McGrouther, T. Berra, S. Fisch-Muller, J. Lundberg, J. Sullivan, R. Rodiles, A. Acero, G. Navas, A. Connell, P. Heemstra, M. Mwale, S. Fennessy, D.R. Robertson, R. Cooke, V. Mogollón, P. Béarez, J. Maldonado, A. Manimekalan, D. Nelson, O. Sanjur, W. Lechner, L.A. Wills, J. Sparks, and M. Retzer. I am grateful to L. Hill, A. Ko'ou, P. Unmack, A. Marceniuk, R. Hadiaty, S. Ferdous, N. Lujan, and M. Sierra for providing assistance during field collections. Lab space and assistance was provided by J.W. Armbruster, K.M. Halanych, and C. Oliveira; S.R. Santos, M. Melo, M. Chiachio, K. Abe, N. Lujan, D. Werneke, L. De Souza, S. Ferdous, K. Ray, R. Belcher, E. Borda, A. Janosik, M. Zhong, A. Mahon, D. Thornhill, K. Kocot, J. Cannon, and L. Zhang gave additional lab assistance. I thank A. Acero, G. Orti, P. Unmack, E. Borda, J. Lundberg, and D. Taphorn for valuable comments and suggestions. I am indebted to J.W. Armbruster, K.M. Halanych, M.H. Sabaj, S.R. Santos, and S.A. Bullard for critically reviewing the manuscript.
- Grande L, Eastman JT: A Review of Antarctic ichthyofaunas in the light of new fossil discoveries. Paleontology. 1986, 29: 113-137.Google Scholar
- All Catfish Species Inventory. [http://silurus.acnatsci.org/]
- Ferraris CJ: Checklist of catfishes, recent and fossil (Osteichthyes:Siluriformes), and catalogue of siluriform primary types. Zootaxa. 2007, 548-1418Google Scholar
- Mo T: Anatomy, Relationships and Systematics of the Bagridae (Teleostei: Siluroidei) with a Hypothesis of Siluroid Phylogeny (Theses Zoologicae). 1991, Koenigstein: Koeltz, 17:Google Scholar
- de Pinna MCC: Phylogenetic relationships of Neotropical Siluriformes (Teleostei: Ostariophysi): historical overview and synthesis of hypotheses. Phylogeny and Classification of Neotropical Fishes. Edited by: Malabarba LR, Reis RE, Vari RP, Lucena ZMS, Lucena CAS. 1998, Porto Alegre: EDIPUCRSGoogle Scholar
- Sullivan JP, Lundberg JG, Hardman M: A phylogenetic analysis of the major groups of catfishes (Teleostei:Siluriformes) using rag1 and rag2 nuclear gene sequences. Mol Phylogenet Evol. 2006, 41 (3): 636-662.PubMedGoogle Scholar
- Gayet M, Meunier FJ: Paleontology and palaeobiogeography of catfishes. Catfishes. Edited by: Arratia G, Kapoor BG, Chardon M, Diogo R. 2003, Enfield, NH: Science Publishers, 2: 491-522.Google Scholar
- Briggs JC: The biogeography of otophysan fishes (Ostariophysi:Otophysi): a new appraisal. J Biogeogr. 2005, 32 (2): 287-294.Google Scholar
- Peng ZG, He SP, Wang J, Wang W, Diogo R: Mitochondrial molecular clocks and the origin of the major Otocephalan clades (Pisces:Teleostei): A new insight. Gene. 2006, 370: 113-124.PubMedGoogle Scholar
- Lundberg JG, Sullivan JP, Rodiles-Hernández R, Hendrickson DA: Discovery of African roots for the Mesoamerican Chiapas catfish, Lacantunia enigmatica, requires an ancient intercontinental passage. Proc Acad Nat Sci Phila. 2007, 156: 39-53.Google Scholar
- IUCN red list. [http://www.sci.odu.edu/gmsa]
- Ochi H, Rossiter A, Yanagisawa Y: The first record of a biparental mouthbrooding catfish. J Fish Biol. 2000, 57 (6): 1601-1604.Google Scholar
- Springer VG: Pacific plate biogeography, with special reference to shorefishes. Smithson Contrib Zool. 1982, 367: 1-182.Google Scholar
- Betancur-R R, Armbruster JW: Molecular clocks provide new insights into the evolutionary history of galeichthyine sea catfishes. Evolution. 2009, 63 (5): 1232-1243.PubMedGoogle Scholar
- Kailola PJ: A phylogenetic exploration of the catfish family Ariidae. The Beagle, Rec Mus Art Galleries N Terr. 2004, 20: 87-166.Google Scholar
- Diogo R: Morphological, evolution, aptations, homoplasies, constraints and evolutionary trends: catfishes as a case study on general plylogeny and macroevolution. 2004, Enfield: Science PublishersGoogle Scholar
- Acero PA, Betancur-R R: Monophyly, affinities, and subfamilial clades of the sea catfishes (Siluriformes: Ariidae). Ichthyol Explor Freshwaters. 2007, 18 (2): 133-143.Google Scholar
- Betancur-R R, Acero A, Mejía-Ladino LM: Sistemática filogenética preliminar de algunos bagres marinos (Siluriformes: Ariidae) neotropicales. Mem Fund La Salle Cien Nat. 2004, 158: 61-85.Google Scholar
- Betancur-R R, Acero PA, Bermingham E, Cooke R: Systematics and biogeography of New World sea catfishes (Siluriformes: Ariidae) as inferred from mitochondrial, nuclear, and morphological evidence. Mol Phylogenet Evol. 2007, 45 (1): 339-357.PubMedGoogle Scholar
- Marceniuk AP: Relações Filogenéticas e Revisão dos Gêneros da Família Ariidae (Ostariophysi, Siluriformes). Ph.D. Dissertation. 2003, São Paulo: Universidade de São PauloGoogle Scholar
- Marceniuk AP, Menezes NA: Systematics of the family Ariidae (Ostariophysi, Siluriformes), with a redefinition of the genera. Zootaxa. 2007, 3-126. 1416Google Scholar
- Betancur-R R, Acero A: A new species of Notarius (Siluriformes: Ariidae) from the Colombian Pacific. Zootaxa. 2006, 1249: 47-59.Google Scholar
- Hardman M: The phylogenetic relationships among non-diplomystid catfishes as inferred from mitochondrial cytochrome b sequences; the search for the ictalurid sister taxon (Otophysi:Siluriformes). Mol Phylogenet Evol. 2005, 37 (3): 700-720.PubMedGoogle Scholar
- Betancur-R R, Acero A: Description of Notarius biffi n. sp. and redescription of N. insculptus (Jordan and Gilbert) (Siluriformes: Ariidae) from the eastern Pacific, with evidence of monophyly and limits of Notarius. Zootaxa. 2004, 703: 1-20.Google Scholar
- Hardman M: Phylogenetic relationships among species of Ictaluridae (Otophysi: Siluriformes) and of the family to other catfishes. Ph.D. Dissertation. 2002, Urbana-Champaign: University of IllinoisGoogle Scholar
- Inoue JG, Miya M, Venkatesh B, Nishida M: The mitochondrial genome of Indonesian coelacanth Latimeria menadoensis (Sarcopterygii:Coelacanthiformes) and divergence time estimation between the two coelacanths. Gene. 2005, 349: 227-235.PubMedGoogle Scholar
- Noack K, Zardoya R, Meyer A: The complete mitochondrial DNA sequence of the bichir (Polypterus ornatipinnis), a basal ray-finned fish: Ancient establishment of the consensus vertebrate gene order. Genetics. 1996, 144 (3): 1165-1180.PubMed CentralPubMedGoogle Scholar
- Venkatesh B, Erdmann MV, Brenner S: Molecular synapomorphies resolve evolutionary relationships of extant jawed vertebrates. Proc Natl Acad Sci USA. 2001, 98 (20): 11382-11387.PubMed CentralPubMedGoogle Scholar
- Calcagnotto D, Schaefer SA, DeSalle R: Relationships among characiform fishes inferred from analysis of nuclear and mitochondrial gene sequences. Mol Phylogenet Evol. 2005, 36 (1): 135-153.PubMedGoogle Scholar
- Bermingham E, Martin AP: Comparative mtDNA phylogeography of neotropical freshwater fishes: testing shared history to infer the evolutionary landscape of lower Central America. Mol Ecol. 1998, 7 (4): 499-517.PubMedGoogle Scholar
- Saitoh K, Miya M, Inoue JG, Ishiguro NB, Nishida M: Mitochondrial genomics of ostariophysan fishes: Perspectives on phylogeny and biogeography. J Mol Evol. 2003, 56 (4): 464-472.PubMedGoogle Scholar
- Peng ZG, Wang J, He SP: The complete mitochondrial genome of the helmet catfish Cranoglanis bouderius (Silurifonnes:Cranoglanididae) and the phylogeny of otophysan fishes. Gene. 2006, 376 (2): 290-297.PubMedGoogle Scholar
- Hardman M, Lundberg JG: Molecular phylogeny and a chronology of diversification for "phractocephaline" catfishes (Siluriformes:Pimelodidae) based on mitochondrial DNA and nuclear recombination activating gene 2 sequences. Mol Phylogenet Evol. 2006, 40 (2): 410-418.PubMedGoogle Scholar
- Stenstrom CM, Holmgren E, Isaksson LA: Cooperative effects by the initiation codon and its flanking regions on translation initiation. Gene. 2001, 273 (2): 259-265.PubMedGoogle Scholar
- Edwards SV: Is a new and general theory of molecular systematics emerging?. Evolution. 2009, 63 (1): 1-19.PubMedGoogle Scholar
- Edwards SV, Liu L, Pearl DK: High-resolution species trees without concatenation. Proc Natl Acad Sci USA. 2007, 104 (14): 5936-5941.PubMed CentralPubMedGoogle Scholar
- Whitfield JB, Lockhart PJ: Deciphering ancient rapid radiations. Trends Ecol Evol. 2007, 22 (5): 258-265.PubMedGoogle Scholar
- Hennig W: Phylogenetic systematics. 1966, Urbana: University of Illinois Press, 263-Google Scholar
- Betancur-R R, Marceniuk AP, Béarez P: Taxonomic status and redescription of the Gillbacker Sea Catfish (Siluriformes: Ariidae: Sciades parkeri). Copeia. 2008, 2008 (4): 827-835.Google Scholar
- Kailola PJ: Ariidae. FAO Species Identification Guides for Fishery Purposes: The Living Marine Resources of the Western Central Pacific. Edited by: Carpenter KE, Niem VH. 1999, Rome: FAO, 1827-1879.Google Scholar
- Acero PA: Ariidae. FAO Species Identification Guides for Fishery Purposes: The living Marine Resources of the Western Central Atlantic. Edited by: Carpenter KE. 2002, Rome: FAO, 831-852.Google Scholar
- Betancur-R R, Willink PW: A new freshwater ariid (Otophysi: Siluriformes) from the Río Usumacinta basin. Copeia. 2007, 2007 (4): 818-828.Google Scholar
- Marceniuk AP: Description of Cathorops manglarensis, a new species from the Colombian Pacific, with redescription of Cathorops multiradiatus (Siluriformes; Ariidae). Zootaxa. 2007, 1529: 33-48.Google Scholar
- Marceniuk AP, Betancur-R R: Revision of the species of the genus Cathorops (Siluriformes; Ariidae) from Mesoamerica and the Central American Caribbean, with description of three new species. Neotrop Ichthyol. 2008, 6 (1): 25-44.Google Scholar
- Teugels GG: Taxonomy, phylogeny and biogeography of catfishes (Ostariophysi, Siluroidei): An overview. Aquat Living Resour. 1996, 9: 9-34.Google Scholar
- de Queiroz A: The resurrection of oceanic dispersal in historical biogeography. Trends Ecol Evol. 2005, 20 (2): 68-73.PubMedGoogle Scholar
- McGlone MS: Goodbye Gondwana. J Biogeogr. 2005, 32 (5): 739-740.Google Scholar
- Sparks JS, Smith WL: Phylogeny and biogeography of the Malagasy and Australasian rainbowfishes (Teleostei:Melanotaenioidei): Gondwanan vicariance and evolution in freshwater. Mol Phylogenet Evol. 2004, 33 (3): 719-734.PubMedGoogle Scholar
- Sparks JS, Smith WL: Freshwater fishes, dispersal ability, and nonevidence: "Gondwana Life Rafts" to the rescue. Syst Biol. 2005, 54 (1): 158-165.PubMedGoogle Scholar
- Lee TY, Lawver LA: Cenozoic plate reconstruction of Southeast Asia. Tectonophysics. 1995, 251 (1–4): 85-Google Scholar
- McLoughlin S: The breakup history of Gondwana and its impact on pre-Cenozoic floristic provincialism. Aust J Bot. 2001, 49 (3): 271-300.Google Scholar
- Golani D, Sonin O: The occurrence of the tropical west African marine fishes Acanthurus monroviae (Acanthuridae) and Arius parkii (Ariidae) in the Levant. Aqua J Ichthy Aqua Biol. 1996, 2 (1): 1-3.Google Scholar
- Pitman WCI, Cande S, La Brecque J, Pindell SC: Fragmentation of Gondwana: the separation of Africa and South America. Biological Relationships Between Africa and South America. Edited by: Goldblatt P. 1993, New Haven: Yale University Press, 15-37.Google Scholar
- Maisey JG: Continental break up and the distribution of fishes of Western Gondwana during the Early Cretaceous. Cretac Res. 2000, 21 (2–3): 281-314.Google Scholar
- Smith AG, Smith DG, Funnell BM: Atlas of Mesozoic and Cenozoic coastlines. 1994, New York: Cambridge University PressGoogle Scholar
- Storey BC: The role of mantle plumes in continental breakup – case-histories from Gondwanaland. Nature. 1995, 377 (6547): 301-308.Google Scholar
- Li ZX, Powell CM: An outline of the palaeogeographic evolution of the Australasian region since the beginning of the Neoproterozoic. Earth-Sci Rev. 2001, 53 (3–4): 237-277.Google Scholar
- Hay WW, DeConto RM, Wold CN, Wilson KM, Voigt S, Schulz M, Rossby Wold A, Dullo WC, Ronov AB, Balukhovsky AN, et al: An alternative global Cretaceous paleogeography. Evolution of the Cretaceous Ocean/Climate System. 1999, Geological Society of America Special Paper, 332: 1-47.Google Scholar
- Bellwood DR, Wainwright PC: The history and biogeography of fishes on coral reefs. Coral Reef Fishes: Dynamics and Diversity in a Complex Ecosystem. Edited by: Sale PF. 2002, New York: Academic Press, 5-32.Google Scholar
- Vences M, Freyhof J, Sonnenberg R, Kosuch J, Veith M: Reconciling fossils and molecules: Cenozoic divergence of cichlid fishes and the biogeography of Madagascar. J Biogeogr. 2001, 28 (9): 1091-1099.Google Scholar
- Azuma Y, Kumazawa Y, Miya M, Mabuchi K, Nishida M: Mitogenomic evaluation of the historical biogeography of cichlids toward reliable dating of teleostean divergences. BMC Evol Biol. 2008, 8 (1): 215-PubMed CentralPubMedGoogle Scholar
- Genner MJ, Seehausen O, Lunt DH, Joyce DA, Shaw PW, Carvalho GR, Turner GF: Age of cichlids: New dates for ancient lake fish radiations. Mol Biol Evol. 2007, 24 (5): 1269-1282.PubMedGoogle Scholar
- Briggs JC: Fishes and birds: Gondwana life rafts reconsidered. Syst Biol. 2003, 52 (4): 548-553.PubMedGoogle Scholar
- Cione AL, Prasad GVR: The oldest known catfish (Teleostei:Siluriformes) from Asia (India, Late Cretaceous). J Paleontol. 2002, 76 (1): 190-193.Google Scholar
- American Society of Ichthyologists and Herpetologists. [http://www.asih.org/codons.pdf]
- Hardman M, Page LM: Phylogenetic relationships among bullhead catfishes of the genus Ameiurus (Siluriformes:Ictaluridae). Copeia. 2003, 20-33. 1Google Scholar
- Swofford DL: PAUP*: Phylogenetic Analysis Using Parsimony (*and Other Methods), version 4.0 Beta. Sunderland, MA: Sinauer Associates. 2002Google Scholar
- Posada D, Crandall KA: MODELTEST: testing the model of DNA substitution. Bioinformatics. 1998, 14 (9): 817-818.PubMedGoogle Scholar
- Zwickl DJ: Genetic algorithm approaches for the phylogenetic analysis of large biological sequence datasets under the maximum likelihood criterion. Ph.D. dissertation. 2006, The University of Texas at AustinGoogle Scholar
- Stamatakis A: RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics. 2006, 22 (21): 2688-2690.PubMedGoogle Scholar
- CIPRES portal. [http://www.phylo.org/]
- Ronquist F, Huelsenbeck JP: MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003, 19 (12): 1572-1574.PubMedGoogle Scholar
- Drummond AJ, Ho SYW, Rawlence N, Rambaut A: A rough guide to BEAST 1.4. 2007, Edinburgh: University of EdinburghGoogle Scholar
- Shimodaira H, Hasegawa M: Multiple comparisons of log-likelihoods with applications to phylogenetic inference. Mol Biol Evol. 1999, 16 (8): 1114-1116.Google Scholar
- Ronquist F: Dispersal-vicariance analysis: A new approach to the quantification of historical biogeography. Syst Biol. 1997, 46 (1): 195-203.Google Scholar
- Nelson G, Platnick N: Systematics and biogeography: cladistics and vicariance. 1981, New York: Columbia University PressGoogle Scholar
- Page RDM: Quantitative cladistic biogeography – constructing and comparing area cladograms. Syst Zool. 1988, 37 (3): 254-270.Google Scholar
- Morrone JJ, Crisci JV: Historical biogeography – introduction to methods. Annu Rev Ecol Syst. 1995, 26: 373-401.Google Scholar
- Page RDM: Maps between trees and cladistic-analysis of historical associations among genes, organisms, and areas. Syst Biol. 1994, 43 (1): 58-77.Google Scholar
- Page RDM: COMPONENT Version 2.0. User's Guide. 1993, London: The Natural History Museum, [http://taxonomy.zoology.gla.ac.uk/rod/cplite/Manual.html]Google Scholar
- van Veller MGP, Zandee M, Kornet DJ: Two requirements for obtaining valid common patterns under different assumptions in vicariance biogeography. Cladistics. 1999, 15 (4): 393-406.Google Scholar
- Sanderson MJ: r8s: inferring absolute rates of molecular evolution and divergence times in the absence of a molecular clock. Bioinformatics. 2003, 19 (2): 301-302.PubMedGoogle Scholar
- Sanderson MJ: r8s, version 1.70, User's Manual. 2004, [http://loco.biosci.arizona.edu/r8s/r8s1.7.manual.pdf]Google Scholar
- Thorne JL, Kishino H: Divergence time and evolutionary rate estimation with multilocus data. Syst Biol. 2002, 51 (5): 689-702.PubMedGoogle Scholar
- Drummond AJ, Ho SYW, Phillips MJ, Rambaut A: Relaxed phylogenetics and dating with confidence. PLoS Biol. 2006, 4 (5): 699-710.Google Scholar
- Hurley IA, Mueller RL, Dunn KA, Schmidt EJ, Friedman M, Ho RK, Prince VE, Yang ZH, Thomas MG, Coates MI: A new time-scale for ray-finned fish evolution. Proc R Soc B-Biol Sci. 2007, 274 (1609): 489-498.Google Scholar
- Kumazawa Y, Azuma Y, Nishida M: Tempo of mitochondrial gene evolution: Can mitochondrial DNA be used to date old divergences?. Endocyt Cell Res. 2004, 15: 136-142.Google Scholar
- Kumar S, Hedges SB: A molecular timescale for vertebrate evolution. Nature. 1998, 392 (6679): 917-920.PubMedGoogle Scholar
- Botella H, Blom H, Dorka M, Ahlberg PE, Janvier P: Jaws and teeth of the earliest bony fishes. Nature. 2007, 448 (7153): 583-586.PubMedGoogle Scholar
- Lundberg JG, Marshall LG, Guerrero J, Horton B, Malabarba MC, Wesselingh F: The stage for Neotropical fish diversification: a history of tropical South American rivers. Phylogeny and Classification of Neotropical Fishes. Edited by: Malabarba LR, Reis RE, Vari RP, Lucena ZMS, Lucena CAS. 1998, Porto Alegre: EDIPUCRS, 13-48.Google Scholar
- Aguilera O, de Aguilera DR: Amphi-American Neogene sea catfishes (Siluriformes, Ariidae) from northern South America. Fossils of the Miocene Castillo Formation, Venezuela: Contributions on Neotropical Palaeontology. Edited by: Sánchez-Villagra MR, Clack JA. 2004, Special Papers in Palaeontology, 71: 29-48.Google Scholar
- Bermingham E, McCafferty SS, Martin AP: Fish biogeography and molecular clocks: perspectives from the Panamanian Isthmus. Molecular Systematics of Fishes. Edited by: Stepien CA, Kocher TD. 1997, New York: Academic Press, 113-128.Google Scholar
- Coates AG, Obando JA: Geologic evolution of the Central American Isthmus. Evolution and Environments in Tropical America. Edited by: Jackson JB, Budd AF, Coates AG. 1996, Chicago: University of Chicago Press, 21-56.Google Scholar
- Near TJ, Bolnick DI, Wainwright PC: Fossil calibrations and molecular divergence time estimates in centrarchid fishes (Teleostei:Centrarchidae). Evolution. 2005, 59 (8): 1768-1782.PubMedGoogle Scholar
- Hedges SB, Kumar S: Precision of molecular time estimates. Trends Genet. 2004, 20 (5): 242-247.PubMedGoogle Scholar
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