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FIGURE 1 in Molecular phylogeny of Diphtherophora de Man, 1880 (Nematoda: Diphtherophoridae), with description of a new species
FIGURE 1. Diagnostic characters of Diphtherophora eldarica n. sp. A–C, F, G, females. D–E, H, males. A, E, body posture. B, pharyngeal region. C, D, anterior end. G, H, posterior end.
FIGURE 3 in Molecular phylogeny of Diphtherophora de Man, 1880 (Nematoda: Diphtherophoridae), with description of a new species
FIGURE 3. Diagnostic characters of Diphtherophora caudata females (A, E) and males (I, L); Diphtherophora geraerti females (B, F) and males (J, M); Diphtherophora perplexans females (C, G); and Diphtherophora tenera females (D, H) and males (K, N), all recovered from Iran. A-D, I-K, anterior end. E-H, L-N, posterior end. (Scale-bars: A-N = 10 µm).
FIGURE 2 in Molecular phylogeny of Diphtherophora de Man, 1880 (Nematoda: Diphtherophoridae), with description of a new species
FIGURE 2. Diagnostic characters of Diphtherophora eldarica n. sp. A–C, F–H, K, M–O, females. D–E, I–J, L, P, males. A, E, body posture. B, C, D, anterior end. F, J, pharyngeal region. G, H, I, ventromedian papillae. K, L, spermatozoa. M, N, P, posterior end. (Scale-bars: B–D, G–I, K–P = 10 µm; A, E, F and J = 50 µm).
FIGURE 2 in Molecular phylogeny of Asian pipesnakes, genus Cylindrophis Wagler, 1828 (Squamata: Cylindrophiidae), with the description of a new species from Myanmar
FIGURE 2. Maximum likelihood (ML) trees of Cylindrophis. Yellow and green circles represent bootstrap support values of 70–94 (moderate support) and 95–100 (strong support), respectively. Clades without circles represent bootstrap values of 0–69 (poor support). Scale bars indicate the estimation of nucleotide substitutions per site. For each terminal, a voucher number and political unit (country) are given. For specimens from Indonesia (ID), island localities are additionally provided. A purple star (★) represents specimens of the new species described herein. A) Concatenated ML phylogeny of Cylindrophis using 16S, ND2, and R35 loci. The shaded clade highlights a Wallacean group containing C. isolepis, C. boulengeri, and C. yamdena. B–D) ML genealogies using 16S (B), ND2 (C), and R35 (D). Photo credits: Cylindrophis maculatus: Ruchira Somaweera (The Commonwealth Scientific and Industrial Research Organisation/CSIRO); Cylindrophis sp. nov. (holotype designated herein, CAS 241554): Justin M. Bernstein (Rutgers University-Newark); C. burmanus: Hla Tun (photograph registered and archived at CAS: ID: MHS_209); C. jodiae: Teo Eng Wah (University of Malaya); C. isolepis: Jimmy A. McGuire (MVZ); C. boulengeri: Sven Mecke (Naturkundemuseum Paderborn); C. yamdena: Ron E. Johnstone (WAM).
FIGURE 5 in Molecular phylogeny of Asian pipesnakes, genus Cylindrophis Wagler, 1828 (Squamata: Cylindrophiidae), with the description of a new species from Myanmar
FIGURE 5. Collection localities of the specimens of Cylindrophis burmanus (green symbols) and Cylindrophis slowinskii (blue circles) used for our molecular analyses. Symbols in the maps correspond to the ones used for the different clades in the accompanying tree. Major clades of C. burmanus are distinguished by green circles and squares. The orange diamond represents the collection locality of the lectotype of C. burmanus (BMNH 1940.3.3.1 from Yangon (Rangoon); specimen not included in phylogenetic analysis). In the country map of Myanmar, higher elevations appear in brighter and lower elevations in darker shades of green; the Chindwin and Irrawaddy Rivers are marked in yellow and purple, respectively; the Arakan Mountain range is highlighted with yellow triangles. The satellite map is a detailed magnification of the area shaded purple in the country map. An arrow in the inset map indicates where the Irrawaddy splits into its delta. Note that the three green squares in the satellite image represent near-overlapping localities of the southern population of C. burmanus that appear as a single symbol in the larger map. Satellite map obtained from Google Earth v7.3.2.5776: Image © 2019 TerraMetrics Data SIO, NOAA, U.S. Navy, NGA, GEBCO. Map prepared by Justin M. Bernstein.
FIGURE 3 in Molecular phylogeny of Asian pipesnakes, genus Cylindrophis Wagler, 1828 (Squamata: Cylindrophiidae), with the description of a new species from Myanmar
FIGURE 3. Concatenated (left) and species (right) trees of Cylindrophis. Open circles (○) indicate ML bootstrap values of 70–94; filled circles (●) represent ML bootstrap values of 95–100 (concatenated) or PP of 0.95–1 (BEAST). Symbols behind each clade refer to taxa as defined in inset, with symbols for species of the Wallacean clade consistently colored red. In the map, the origins, as political units (countries) or islands, of the specimens used for the phylogenies are shaded, and do not represent the total geographic range of the respective taxon. A purple star (★) indicates the type locality of the new species described herein. For country records of all species of Cylindrophis, see Fig. 1.
FIGURE 4 in Molecular phylogeny of Asian pipesnakes, genus Cylindrophis Wagler, 1828 (Squamata: Cylindrophiidae), with the description of a new species from Myanmar
FIGURE 4. Holotype of Cylindrophis slowinskii sp. nov. (CAS 241554) from Kachin State, Myanmar in dorsal (A) and ventral (B) view. The head is shown in lateral (C) and dorsal (D) view, the tail in ventral view (E). The 10 mm and 5 mm scale bars are for panels A+B and C+D+E, respectively. Photos by Justin M. Bernstein.
Data from: Molecular phylogeny of the Taeniapterini (Diptera: Micropezidae) using nuclear and mitochondrial DNA, with a reclassification of the genus Taeniaptera Macquart
DNA molecular data are used to generate a phylogeny for the micropezid subfamily Taeniapterinae. Thirty-two taeniapterine species were sampled, including 10 of the 20 New World genera recognized by Steyskal, as well as one genus formerly treated as a synonym of Poecilotylus Hennig (Hemichaeta Steyskal). Five species from the Micropezinae were included as outgroups. A total DNA dataset of 4705 bp, including mitochondrial genes (12S and cytochrome c oxidase I (COI)) and nuclear coding genes (wingless and CAD), was analysed using maximum parsimony and Bayesian inference. The genus Taeniaptera Macquart was found to be non-monophyletic with respect to the remainder of the Taeniapterini analysed here. Taeniaptera is restricted to the Taeniaptera trivittata Macquart species group, Mitromyia Cresson is resurrected to contain the Taeniaptera grata (Wulp) species group, and Paragrallomyia Hendel is resurrected to contain most species previously considered Taeniaptera. Poecilotylus is recognized as a paraphyletic group awaiting further research.
Data from: A molecular phylogeny of Eumorpha (Lepidoptera: Sphingidae) and the evolution of anti-predator larval eyespots
Many insects possess conspicuous external circular ring markings that resemble the eye of a vertebrate. These 'eyespots' typically function to startle or otherwise deter predators, but few studies have examined how eyespots have evolved. We study the evolution of the posterior larval eyespot in the charismatic New World hawkmoth genus Eumorpha. While Eumorpha has a range of posterior larval eyespot shapes and sizes, little is known of how this trait has evolved because phylogenetic relationships of Eumorpha remain largely unknown. In this study, we included 62 individuals from 23 of 26 described Eumorpha species, and sequenced four genes (CAD, EF-1α, Wingless and COI), totaling 3773 base pairs. Maximum likelihood and Bayesian phylogenetic methods produced largely congruent trees with well-supported relationships. Our analyses reveal that Eumorpha probably had an ancestor with a posterior larval eyespot and that the eyespot was subsequently lost in at least three lineages. Eumorpha appears to have originated in Central and South America and expanded its distribution to North America.
Data from: A jungle tale: molecular phylogeny and divergence time estimates of the Desmopsis - Stenanona clade (Annonaceae) in Mesoamerica
The predominantly Asian tribe Miliuseae (Annonaceae) includes over 37 Neotropical species that are mainly distributed across Mesoamerica, from southern Mexico to northern Colombia. The tremendous ecological and morphological diversity of this clade, including ramiflory, cauliflory, flagelliflory, and clonality, suggests adaptive radiation. Despite the spectacular phenotypic divergence of this clade, little is known about its phylogenetic and evolutionary history. In this study we used a nuclear DNA marker and seven chloroplast markers, and maximum parsimony, maximum likelihood and Bayesian inference methods to reconstruct a comprehensive time-calibrated phylogeny of tribe Miliuseae, especially focusing on the Desmopsis-Stenanona clade. We also perform ancestral area reconstructions to infer the biogeographic history of this group. Finally, we use ecological niche modeling, lineage distribution models, and niche overlap tests to assess whether geographic isolation and ecological specialization influenced the diversification of lineages within this clade. We reconstructed a monophyletic Miliuseae that is divided into two strongly supported clades: (i) a Sapranthus-Tridimeris clade and (ii) a Desmopsis-Stenanona clade. The colonization of the Neotropics and subsequent diversification of Neotropical Miliuseae seems to have been associated with the expansion of the boreotropical forests during the late Eocene and their subsequent fragmentation and southern displacement. Further speciation within Neotropical Miliuseae out of the Maya block seems to have occurred during the last 15 million years. Lastly, the geographic structuring of major lineages of the Desmopsis-Stenanona clade seems to have followed a climatic gradient, supporting the hypothesis that morphological differentiation between closely related species resulted from both long-term isolation between geographic ranges and adaptation to environmental conditions.
Data from: Phylogeny of salmonids (salmoniformes: Salmonidae) and its molecular dating: analysis of mtDNA data
Phylogenetic relationships among 41 species of salmonid fish and some aspects of their diversification-time history were studied using the GenBank and original mtDNA data. The position of the root of the Salmonidae phylogenetic tree was uncertain. Among the possible variants, the most reasonable seems to be that in which thymallins are grouped into the same clade as coregonins and the lineage of salmonins occupied a basal position relative to this clade. The genera of Salmoninae formed two distinct clades, i.e., (Brachymystax, Hucho) and (Salmo, Parahucho, (Salvelinus, (Parasalmo, Oncorhynchus)). Furthermore, the genera Parasalmo and Oncorhynchus were reciprocally monophyletic. The congruence of Salmonidae phylogenetic trees obtained using different types of phylogenetic markers is discussed. According to Bayesian dating, ancestral lineages of salmonids and their sister esocoids diverged about 106 million years ago. Sometime after, probably 100–70 million years ago, the salmonid-specific whole genome duplication took place. The divergence of salmonid lineages on the genus level occurred much later, within the time interval of 42–20 million years ago. The main wave of the diversification of salmonids at the species level occurred during the last 12 million years. The possible effect of genome duplication on the Salmonidae diversification pattern is discussed.
Data from: A multilocus molecular phylogeny for the avian genus Liocichla (Passeriformes: Leiothrichidae: Liocichla)
Background: Historically the babblers have been assigned to the family Timaliidae but several recent studies have attempted to rest the taxonomy of this diverse passerine assemblage on a more firm evolutionary footing. The result has been a major rearrangement of the group. A well-supported and comprehensive phylogeny for this widespread avian group is an important part of testing evolutionary and biogeographic hypotheses, especially in Asia where the babblers are a key component of many forest ecosystems. However, the genus Liocichla is poorly represented in these prior studies of babbler systematics. Methods: We used a multilocus molecular genetic approach to generate a phylogenetic hypothesis for all five currently recognized species in the avian genus Liocichla. Multilocus DNA sequence data was used to construct individual gene trees using maximum likelihood and species trees were estimated from gene trees using Bayesian analyses. Divergence dates were obtained using a molecular clock approach. Results: Molecular data estimate a probable window of time for the origin for the Liocichla from the mid to late Miocene, between 5.55 and 12.87 Ma. Despite plumage similarities between the insular Taiwan endemic, L. steerii, and the continental L. bugunorum and L. omeiensis, molecular data suggest that L. steerii is the sister taxon to all continental Liocichla. The continental Liocichla are comprised of two lineages; a lineage containing L. omeiensis and L. bugunorum and a lineage comprised of L. phoenicea and L. ripponi. The comparatively early divergence of L. steerii within the Liocichla may be illusory due to extinct and therefore unsampled lineages. L. ripponi and L. phoenicea are parapatric with a Pleistocene split (0.07–1.88 Ma) occurring between an Eastern Himalayan L. phoenicea and a Northern Indochina distributed L. ripponi. L. bugunorum and L. omeiensis underwent a similar split between the Eastern Himalaya (L. bugunorum) and Central China (L. omeiensis) divided by the Hengduan Mountains. Conclusions: This study supports an origin of the Liocichla occurring sometime prior to the Miocene–Pliocene boundary, a period of significant climatic upheaval in Asia. The biogeographical patterns within the Liocichla mirror those of other birds in the region and allude to common geological and climatic drivers of avian diversification in Asia.
Data from: Molecular phylogeny of the highly diversified catfish subfamily Loricariinae (Siluriformes, Loricariidae) reveals incongruences with morphological classification
The Loricariinae belong to the Neotropical mailed catfish family Loricariidae, the most species-rich catfish family. Among loricariids, members of the Loricariinae are united by a long and flattened caudal peduncle and the absence of an adipose fin. Despite numerous studies of the Loricariidae, there is no comprehensive phylogeny of this morphologically highly diversified subfamily. To fill this gap, we present a molecular phylogeny of this group, including 350 representatives, based on the analysis of mitochondrial and nuclear genes (8426 positions). The resulting phylogeny indicates that Loricariinae are distributed into two sister tribes: Harttiini and Loricariini. The Harttiini tribe, as classically defined, constitutes a paraphyletic assemblage and is here restricted to the three genera Harttia, Cteniloricaria, and Harttiella. Two subtribes are distinguished within Loricariini: Farlowellina and Loricariina. Within Farlowellina, the nominal genus formed a paraphyletic group, as did Sturisoma and Sturisomatichthys. Within Loricariina, Loricaria, Crossoloricaria, and Apistoloricaria are also paraphyletic. To solve these issues, and given the lack of clear morphological diagnostic features, we propose here to synonymize several genera (Quiritixys with Harttia; East Andean members of Crossoloricaria, and Apistoloricaria with Rhadinoloricaria; Ixinandria, Hemiloricaria, Fonchiiichthys, and Leliella with Rineloricaria), to restrict others (Crossoloricaria, and Sturisomatichthys to the West Andean members, and Sturisoma to the East Andean species), and to revalidate the genus Proloricaria.
Data from: Molecular phylogeny and diversification timing of the Nemouridae family (Insecta, Plecoptera) in the Japanese Archipelago
The generation of the high species diversity of insects in Japan was profoundly influenced by the formation of the Japanese Archipelago. We explored the species diversification and biogeographical history of the Nemouridae Billberg, 1820 family in the Japanese Archipelago using mitochondrial DNA and nuclear DNA markers. We collected 49 species among four genera: Indonemoura Baumann, 1975; Protonemura Kempny, 1898; Amphinemura, Ris 1902 and Nemoura Latreille, 1796 in Japan, China, South Korea and North America. We estimated their divergence times—based on three molecular clock node calibrations—using Bayesian phylogeography approaches. Our results suggested that Japanese Archipelago formation events resulted in diversification events in the middle of the Cretaceous (<120 Ma), speciation in the Paleogene (<50 Ma) and intra-species diversification segregated into eastern and western Japan of the Fossa Magna region at late Neogene (20 Ma). The Indonemoura samples were genetically separated into two clades—that of Mainland China and that of Japan. The Japanese clade clustered with the Nemouridae species from North America, suggesting the possibility of a colonisation event prior to the formation of the Japanese Archipelago. We believe that our results enhanced the understanding both of the origin of the species and of local species distribution in the Japanese Archipelago.
Data from: Molecular phylogeny of Tragopogon L. (Asteraceae) based on seven nuclear loci (Adh, GapC, LFY, AP3, PI, ITS, and ETS)
Tragopogon is a large Eurasian genus of approximately 150 species. Despite the use of 6910 aligned bp of sequence data representing seven loci, relationships within the genus remain largely unresolved. The young age of the genus in combination with rapid diversification may be the best explanation for this poor resolution. Our studies have revealed that Geropogon is well supported as the immediate sister to Tragopogon. Sections Tragopogon, Brevirostris, Chromopappus, and Hebecarpus of traditional taxonomic treatments are largely monophyletic; sections Angustissimi, Majores, Collini, and Profundisulcati are non-monophyletic. The monotypic sections Macropogon, Dasypogon, and Dybjanskya appear within other sections and no longer merit recognition. Our molecular investigations of geographically widespread species in Europe, including T. crocifolius, T. pratensis, T. porrifolius, and T. orientalis, indicate that each may be non-monophyletic, comprising several cryptic species. These widespread diploids are the proposed parents of some of the Eurasian allopolyploids, as well as the parents of the recently formed T. mirus and T. miscellus from North America
Data from: Molecular phylogeny of Terniopsis (Podostemaceae) and contrasting molecular and morphological variations in two species
Podostemaceae show different patterns of morphological variation relative to molecular ones between genera and between species, but additional material was necessary to make the patterns clearer. Using new material collected from Cambodia, we compared the variations of Terniopsis chanthaburiensis and T. heterostaminata in Cambodia, Laos and Thailand, and conducted matK phylogenetic analysis with many samples and most species of the genus. In contrast to the narrow molecular variation, the morphological variation (e.g., in the length of the shoots and pedicels) is large and continuous. The results indicate that variation in the two species is intraspecific. A similar pattern exists in two pairs of other species of Terniopsis, in which the morphological variation is large and discontinuous, while there is little molecular difference. The opposite pattern is present in other cases (e.g., Dalzellia zeylanica and Tristicha trifaria). The variation in T. chanthaburiensis and T. heterostaminata does not appear to be a response to variation in the habitats, that is submerged rock surfaces in fast currents. Distributional and phylogenetic data indicate that Terniopsis diversified primarily in Laos and Thailand, then expanded into neighboring regions. A synopsis of the genus Terniopsis and its 14 species is given.
Data from: Molecular phylogeny and phylogeography of the Australian freshwater fish genus Galaxiella, with an emphasis on dwarf Galaxias (G. pusilla)
The freshwater fauna of Southern Australia is primarily restricted to the southwestern and southeastern corners of the continent, and is separated by a large, arid region that is inhospitable to this biota. This geographic phenomenon has attracted considerable interest from biogeographers looking to explain evolutionary diversification in this region. Here, we employed phylogenetic and phylogeographic approaches to evaluate the effect of this barrier on a group of four galaxiid fish species (Galaxiella) endemic to temperate Southern Australia. We also tested if continental shelf width has influenced connectivity among populations during low sea levels when rivers, now isolated, could have been connected. We addressed these questions by sampling each species across its range using multiple molecular markers (mitochondrial cytochrome b sequences, nuclear S7 intron sequences, and 49 allozyme loci). These data also allowed us to assess species boundaries, to refine phylogenetic affinities, and to estimate species ages. Interestingly, we found compelling evidence for cryptic species in G. pusilla, manifesting as allopatric eastern and western taxa. Our combined phylogeny and dating analysis point to an origin for the genus dating to the early Cenozoic, with three of the four species originating during the Oligocene-Miocene. Each Galaxiella species showed high levels of genetic divergences between all but the most proximate populations. Despite extensive drainage connections during recent low sea levels in southeastern Australia, populations of both species within G. pusilla maintained high levels of genetic structure. All populations experienced Late Pleistocene-Holocene population growth, possibly in response to the relaxation of arid conditions after the last glacial maximum. High levels of genetic divergence and the discovery of new cryptic species have important implications for the conservation of this already threatened group of freshwater species.
Data from: Molecular phylogeny of rhynchonellide articulate brachiopods (Brachiopoda, Rhynchonellida)
We present here the first report based on phylogenetic analyses of small subunit (SSU/18S) and large subunit (LSU/28S) ribosomal DNA (rDNA) sequences from a wider-than-token sample of rhynchonellide articulate brachiopods, with data from 11 of ∼20 extant genera (12 species) belonging to all four extant superfamilies. Data exploration by network and saturation analyses shows that the molecular sequence data are free from major aberrations and are suitable for phylogenetic reconstruction despite the presence of large deletions in four SSU rDNA sequences. Although molecular sequence analyses cannot directly illuminate the systematics of fossils, the independent, genealogical evidence and phylogenetic inferences about extant forms that they make possible are highly relevant to paleontological systematics because they highlight the limitations of evolutionary inference from morphology. Parsimony, distance, maximum likelihood (no clock) and Bayesian (relaxed-clock) analyses all find a tree topology that disagrees strongly with the existing superfamily classification. All tested phylogenetic reconstructions agree that the taxa analyzed fall into three clades designated A1, A2, and B that reflect two major divergence events. The relaxed-clock analysis indicates that clades A and B diverged in the Paleozoic, while clades A1 and A2 reflect Permo-Triassic (and later) events. Morphological homoplasy and possible gene co-option are suggested as the main sources for the discord between the morpho-classification, the results of cladistic analyses of morphology, and the relationships reconstructed from molecular sequences. The origin, function and evolutionary implications of the deletion-bearing rhynchonellide SSU rDNA sequences are briefly discussed in relation to pseudogenes and concerted evolution in the rDNA genomic region.
Data from: Molecular phylogeny of an ancient rodent family (Aplodontiidae)
The family Aplodontiidae contains a single, monotypic extant genus, Aplodontia (mountain beaver), which was 1st described by Rafinesque in 1817. Phylogenetic studies have shown that it is the sister lineage to squirrels. Aplodontia rufa is endemic to the Pacific Northwest and ranges from central California to British Columbia. Currently, 7 described subspecies are recognized based on morphological taxonomic studies. In this study, mitochondrial and nuclear genes were sequenced to infer molecular phylogenies of A. rufa. One of the goals of this study was to test the current taxonomic hypothesis based on morphology with molecular data. Another goal was to incorporate geographic information to elucidate distributions of major clades. Our results support the previously held subspecies designations based on morphological taxonomy, with 1 main exception: we determined that within A. rufa, the subspecies A. rufa rainieri and A. rufa rufa north of the Columbia River represent a single lineage and should revert to the name A. rufa olympica. Although we revised geographic boundaries for some groups (A. r. rufa, A. r. olympica, A. r. pacifica), only the conservation status and management of A. r. olympica (previously 2 subspecies) in Canada may be affected. Our findings support the continued conservation efforts for the isolated and endangered lineages present in coastal California.
Data from: A phylogeny and evolutionary natural history of Mesoamerican toads (Anura: Bufonidae: Incilius) based on morphology, life history, and molecular data
We combine mitochondrial and nuclear DNA sequence data with non-molecular (morphological and natural history) data to conduct phylogenetic analyses and generate an evolutionary hypothesis for the relationships among nearly every species of Mesoamerican bufonid in the genus Incilius. We collected a total of 5,898 aligned base-pairs (bp) of sequence data from mitochondrial (mtDNA: 12S–16S, cyt b, ND2–CO1, including tRNAsTRP–TYR and the origin of light strand replication; total 4,317 bp) and nuclear (CXCR4 and RAG1; total 1,581 bp) loci from 52 individuals representing 37 species. For the non-molecular data, we collected 44 characters from 29 species. We also include Crepidophryne, a genus that has not previously been included in molecular analyses. We present results of parsimony and Bayesian analyses for these data separately and combined. Relationships based on the non-molecular data were poorly supported and did not resolve a monophyletic Incilius (Rhinella marina was nested within). Our molecular data provide significant support to most of the relationships. Our combined analyses demonstrate that inclusion of a considerably smaller dataset (44 vs. 5,898 characters) of non-molecular characters can provide significant support where the molecular relationships were lacking support. Our combined results indicate that Crepidophryne is nested within Incilius; therefore, we place the former in the synonymy of the latter taxon. Our study provides the most comprehensive evolutionary framework for Mesoamerican bufonids (Incilius), which we use as a starting point to invoke discussion on the evolution of their unique natural history traits.
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