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14,185 results for “phylogenies”

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dryad36/100

Highly resolved papilionoid legume phylogeny based on plastid phylogenomics

<p>Comprising 501 genera and around 14,000 species, Papilionoideae is not only the largest subfamily of Fabaceae (Leguminosae; legumes), but also one of the most extraordinarily diverse clades among angiosperms. Papilionoids are a major source of food and forage, are ecologically successful in all major biomes, and display dramatic variation in both floral architecture and plastid genome (plastome) structure. Plastid DNA-based phylogenetic analyses have greatly improved our understanding of relationships among the major groups of Papilionoideae, yet the backbone of the subfamily phylogeny remains unresolved. In this study, we sequenced and assembled 39 new plastomes that are covering key genera of evolution and morphological diversity in the subfamily. From 244 total taxa, we produced eight datasets for maximum likelihood (ML) analyses based on entire plastomes and/or concatenated sequences of 77 protein-coding sequences (CDS) and two datasets for multispecies coalescent (MSC) analyses based on individual gene trees. We additionally produced a combined nucleotide dataset comprising CDS plus matK gene sequences only, in which most papilionoid genera were sampled. An ML tree based on the entire plastome maximally supported all of the deep and most recent divergences of papilionoids (223 out of 236 nodes). The Swartzieae, ADA (Angylocalyceae, Dipterygeae, and Amburaneae), Cladrastis, Andira, and Exostyleae clades formed a grade to the remainder of the Papilionoideae, concordant with nine ML and two MSC trees. Phylogenetic relationships among the remaining five papilionoid lineages (Vataireoid, Dermatophyllum, Genistoid s.l., Dalbergioid s.l., and Baphieae + Non-Protein Amino Acid Accumulating or NPAAA clade) remained uncertain, because of insufficient support and/or conflicting relationships among trees. Our study fully resolved most of the deep nodes of Papilionoideae, however some relationships require further exploration. More genome-scale data and rigorous analyses are needed to disentangle phylogenetic relationships among the five remaining lineages.</p>

opencc-zeroFeb 2022View details →
zenodo36/100

Three New Species of Hypoxylon (Xylariales, Ascomycota) on a multigene phylogeny from Medog in China

<p>Figure S1: ML phylogram inferred from ITS-TUB2&nbsp;sequences. ML bootstrap support (BS) &ge; 50% and Bayesian posterior probabilities (PP) &ge; 0.95 are labelled above or below the respective branches (BS/PP). Species in bold were sequenced in the this study.</p>

opencc-by-4.0Apr 2022View details →
dryad36/100

Molecular phylogeny reveals the past transoceanic voyages of drywood termites (Isoptera, Kalotermitidae)

<p><span>Termites are major decomposers in terrestrial ecosystems and the second most diverse lineage of social insects. The Kalotermitidae form the second-largest termite family and are distributed across tropical and subtropical ecosystems, where they typically live in small colonies confined to single wood items inhabited by individuals with no foraging abilities. How the Kalotermitidae have acquired their global distribution patterns remains unresolved. Similarly, it is unclear whether foraging is ancestral to Kalotermitidae or was secondarily acquired in a few species. These questions can be addressed in a phylogenetic framework. We inferred time-calibrated phylogenetic trees of Kalotermitidae using mitochondrial genomes of ~120 species, about 27% of kalotermitid diversity, including representatives of 21 of the 23 kalotermitid genera. Our mitochondrial genome phylogenetic trees were corroborated by phylogenies inferred from nuclear ultraconserved elements derived from a subset of 28 species. We found that extant kalotermitids shared a common ancestor 84 Mya (75–93 Mya 95% HPD), indicating that a few disjunctions among early-diverging kalotermitid lineages may predate Gondwana breakup. However, most of the ~40 disjunctions among biogeographic realms were dated at less than 50 Mya, indicating that transoceanic dispersals, and more recently human-mediated dispersals, have been the major drivers of the global distribution of Kalotermitidae. Our phylogeny also revealed that the capacity to forage is often found in early-diverging kalotermitid lineages, implying the ancestors of Kalotermitidae were able to forage among multiple wood pieces. Our phylogenetic estimates provide a platform for critical taxonomic revision and future comparative analyses of Kalotermitidae.</span></p>

opencc-zeroApr 2022View details →
zenodo36/100

A quantitative assessment of the patterns of integration in the mandible of bovids and their relationships with trophic ecology, phylogeny, and evolutionary rates

<p>Dataset and R script supporting the findings of the study &quot;A&nbsp;quantitative assessment of the patterns of integration in the mandible of bovids and their relationships with trophic ecology, phylogeny, and evolutionary rates&quot;.&nbsp;</p>

opencc-by-4.0Dec 2021View details →
dryad36/100

A new phylogeny of Rumex (Polygonaceae) adds evolutionary context to the diversity of reproductive systems present in the genus

<p><em>Rumex</em> is a unique member of the <em>Polygonaceae</em> family of plants. A source of intrigue for <em>Rumex</em> lies in the diversity of the reproductive systems associated with this genus. Four previously circumscribed subgenera and some two-hundred species comprise the collective <em>Rumex</em> genus. These species exhibit monoecious, dioecious, synoecious (hermaphroditic), and polygamous reproductive systems. Moreover, some of the dioecious species contain heteromorphic sex chromosomes, a phenomenon that is very rare in angiosperms. Apart from these confirmed morphological and phytogeographical distinctions, two of the four described subgenera, <em>Rumex</em> subg. <em>Acetosa</em> and <em>Rumex</em> subg. <em>Acetosella</em>, are distinctive in their sex chromosome systems. For this study, we used three chloroplast markers, <em>rbcL</em>, <em>trnH</em>-<em>psbA</em>, <em>trnL</em>-<em>F</em>, and dense taxon sampling, to reconstruct the most comprehensive molecular phylogeny of <em>Rumex</em> to date. The reconstructed phylogeny for this work resolves six major clades and one large grade in <em>Rumex</em> subg. <em>Rumex</em>. In addition, the species with known dioecious reproductive systems are resolved within a broader clade termed "<em>the dioecious clade</em>". These results suggest that the species with divergent reproductive systems are more closely related to each other than to other species comprising the rest of the <em>Rumex</em> genus. Furthermore, some species with known synoecious reproductive systems are resolved in a single clade which is also nested within "<em>the dioecious clade</em>". These results imply a possible reversal occurring over time which suggests the highly plastic nature of the reproductive systems in <em>Rumex</em> species.</p>

opencc-zeroMay 2022View details →
dryad36/100

The rediscovery of a relict unlocks the first global phylogeny of whip spiders (Amblypygi)

<p>Asymmetrical rates of cladogenesis and extinction abound in the Tree of Life, resulting in numerous minute clades that are dwarfed by larger sister groups. Such taxa are commonly regarded as phylogenetic relicts or "living fossils" when they exhibit an ancient first appearance in the fossil record and prolonged external morphological stasis, particularly in comparison to their more diversified sister groups. Due to their special status, various phylogenetic relicts tend to be well-studied and prioritized for conservation. A notable exception to this trend is found within Amblypygi ("whip spiders"), a visually striking order of functionally hexapodous arachnids that are notable for their antenniform first walking leg pair (the eponymous "whips"). Paleoamblypygi, the putative sister group to the remaining Amblypygi, is known from Late Carboniferous and Eocene deposits, but is survived by a single living species, <em>Paracharon caecus</em> Hansen, 1921, that was last collected in 1899. Due to the absence of genomic sequence-grade tissue for this vital taxon, there is no global molecular phylogeny for Amblypygi to date, nor a fossil-calibrated estimation of divergences within the group. Here, we report several individuals of a previously unknown species of Paleoamblypygi from a cave site in Colombia. Capitalizing upon this discovery, we generated the first molecular phylogeny of Amblypygi, integrating ultraconserved element sequencing with legacy Sanger datasets and including described extant genera. To quantify the impact of sampling Paleoamblypygi on divergence time estimation, we performed in <em>silico</em> experiments with pruning of <em>Paracharon</em>. We demonstrate that the omission of relicts has a significant impact on the accuracy of node dating approaches that outweighs the impact of excluding ingroup fossils. Our results underscore the imperative for biodiversity discovery efforts in elucidating the phylogenetic relationships of " dark taxa", and especially phylogenetic relicts in tropical and subtropical habitats.</p>

opencc-zeroMay 2022View details →
dryad36/100

New non-native pseudocryptic Cyclorhipidion species (Coleoptera: Curculionidae: Scolytinae: Xyleborini) found in the United States as revealed in a multigene phylogeny

<p>Pseudocryptic species, those that are difficult to diagnose using traditional taxonomic methods, are serious impediments for recognizing the introduction of non-native species. Rapid identification of species facilitates a rapid response to newly introduced species which can lessen their damaging effects. This situation is acute for known pest species such as xyleborine ambrosia beetles which are difficult to identify given minute morphological, often variable, diagnostic characters. These beetles have been introduced into non-native temperate regions and have caused economic and ecological havoc. In this study, we produced DNA-based phylogenies using four genes for individuals of <em>Cyclorhipidion bodoanum</em> (Reitter, 1913)<em>, C. distinguendum </em>(Eggers, 1930), and <em>C. pelliculosum </em>(Eichhoff, 1878) sampled from their introduced and native Asian ranges and as well as other <em>Cyclorhipidion </em>species. In addition, we review subtle morphological characters for diagnostic potential for these similar species. Bayesian phylogenetic analysis produced well-resolved and supported phylogeny that provided evidence for multiple introductions of <em>C. bodoanum and C. distinguendum</em> into the US and the occurrence of pseudocryptic species. The ambrosia beetles <em>Cyclorhipidion tenuigraphum </em>(Schedl, 1953)<em> </em>and<em> C. nemesis </em>Smith &amp; Cognato, sp. nov. are reported in North America for the first time. We find that the pattern of elytral interstrial setae is an unrealized source for the identification of <em>Cyclorhipidion</em> species. This study resulted in the recognition of six species adventive to the US with the revised status of <em>C. californicum</em> (Wood, 1975). All species known from North American are diagnosed, illustrated and a key is provided.</p>

opencc-zeroMay 2022View details →
dryad36/100

On the computational reproducibility of molecular phylogenies

<p>Reports on the lack of computational reproducibility of molecular phylogenies, produced in multiple runs of the same program or by different programs, cast a long shadow on downstream research using these phylogenies and on efforts to build the tree of life. We show that this irreproducibility does not decrease the accuracy of the reconstructed evolutionary relationships. Also, we find inferred molecular phylogenies to have log-likelihoods comparable to or better than the true phylogeny. Therefore, the lack of computational reproducibility of molecular phylogenies is not a problem for evolutionary studies.</p>

opencc-zeroMay 2022View details →
dryad36/100

Zehneria neorensis: Additional phylogenies and sequence information

<p>Basic data and supplement for Ranjan et al. 2022, Biogeography of <em>Zehneria</em> (Cucurbitaceae) and a New Species from India, Systematic Botany.</p> <p><em>Zehneria</em> is one of the most diverse genera in Cucurbitaceae with 75 accepted species mainly in Southeast Asia and tropical Africa. We describe <em>Zehneria neorensis</em>, a new species from Neora Valley in the mountains of West Bengal, India, which has 7–10 cm long twisted fruiting pedicels, the longest pedicels reported in the genus so far. Based on morphological data, we also suggest the transfer of <em>Melothria morobensis</em> to the genus <em>Zehneria</em>. With a molecular phylogenetic and global biogeographic analysis based on 3856 nucleotides of plastid and nuclear ribosomal DNA, we demonstrate that the genus <em>Zehneria</em> most likely originated on the African continent 24 (30-19) million years ago and spread from there at least five times to Madagascar and three times to Asia. <em>Zehneria neorensis</em> represents an independent colonization event from Africa to India about 11 (15–7) million years ago. Three lineages reached New Guinea/Australia and finally moved into Polynesia. We infer a rate of at least 20 long-distance dispersal (LDD) events per 10 million years in the genus. This high LDD frequency is most likely a result of the small berry fruits and small flattened seeds of <em>Zehneria</em>, which seem perfectly adapted to long-distance bird dispersal. Field observations are needed to investigate a potential effect of the newly discovered extended and coiling pedicels in <em>Zehneria neorensis</em> on seed dispersal efficiency. The new species adds to a growing list of rather old Cucurbitaceae lineages in the Himalayan foothills, supporting the hypothesis of long climatic stability in the region.</p>

opencc-zeroJun 2022View details →
dryad36/100

Data for a preliminary molecular phylogeny of the family Hydroptilidae (Trichoptera): exploring the combination of targeted enrichment data and legacy Sanger sequence data

<p><span>The purpose of this study is to provide a proof-of-concept that the use of molecular data, particularly targeted enrichment data, and statistically supported methods of analysis can result in the construction of a stable phylogenetic framework for the microcaddisflies (Trichoptera: Hydroptilidae). Here, we use a combination of targeted enrichment data for ca. 300 nuclear protein-coding genes and legacy (Sanger-based) sequence data for the mitochondrial COI gene and partial sequence from the 28S rRNA gene.</span></p>

opencc-zeroJun 2022View details →
dryad36/100

Craniodental morphology and phylogeny of marsupials

<p>The current literature on marsupial phylogenetics includes numerous studies based on analyses of morphological data with limited sampling of Recent and fossil taxa and many studies based on analyses of molecular data with dense sampling of Recent taxa, but few studies have combined both data types. Another dichotomy in the marsupial phylogenetic literature is between studies focused on New World taxa, and those focused on Sahulian taxa. To date, there has been no attempt to assess the phylogenetic relationships of the global marsupial fauna based on combined analyses of morphology and molecular sequences for a dense sampling of Recent and fossil taxa. For this report, we compiled morphological and molecular data from an unprecedented number of Recent and fossil marsupials. Our morphological data consist of 180 craniodental characters that we scored for 97 terminals representing every currently recognized Recent genus, 42 additional ingroup (crown-clade marsupial) terminals represented by well-preserved fossils, and 5 outgroups (nonmarsupial metatherians). Our molecular data comprise 24.5 kb of DNA sequences from whole-mitochondrial genomes and six nuclear loci (<em>APOB</em>, <em>BRCA1</em>, <em>GHR</em>, <em>RAG1</em>, <em>RBP3, </em>and <em>VWF</em>) for 97 marsupial terminals (the same Recent taxa scored for craniodental morphology) and several placental and monotreme outgroups. The results of separate and combined analyses of these data using a wide range of phylogenetic methods support many currently accepted hypotheses of ingroup (marsupial) relationships, but they also underscore the difficulty of placing fossils with key missing data (e.g., †<em>Evolestes</em>), and the unique difficulty of placing others that exhibit mosaics of plesiomorphic and autapomorphic traits (e.g., †<em>Yalkaparidon</em>). Unique contributions of our study are (1) critical discussions and illustrations of marsupial craniodental morphology including features never previously coded for phylogenetic analysis; (2) critical assessments of relative support for many suprageneric clades; (3) estimates of divergence times derived from tip-and-node dating based on uniquely taxon-dense analyses; and (4) a revised, higher-order classification of marsupials accompanied by lists of supporting craniodental synapomorphies. Far from the last word on these topics, this report lays the foundation for future research that may be enabled by the discovery of new fossil taxa, better-preserved material of previously described taxa, novel morphological characters (e.g., from the postcranium), and improved methods of phylogenetic analysis.</p>

opencc-zeroJun 2022View details →
dryad36/100

Genetic variation data to explore the phylogeny of Iberian weedy rice

<p>Weedy rice, a damaging conspecific weed of cultivated rice, has arisen multiple times independently around the world. Understanding all weedy rice origins is necessary to create more effective weed management strategies. The origins of weedy rice in Spain and Portugal, where there are no native <em>Oryza</em> species are unknown. We used genotyping-by-sequencing (GBS) to understand the origin of Iberian weedy rice and its relationship to other weedy, wild, and cultivated rice groups worldwide. This is the variant call format (vcf) file for all 481 accessions including weedy, wild, and cultivated rice. We used this dataset to understand the phylogenetic relationships and population structure among these different populations, especially the Iberian weedy rice. We find that weedy rice in the Iberian Peninsula has primarily evolved through de-domestication of <em>temperate japonica</em> cultivars, with minor origins from exotic weedy rice.</p>

opencc-zeroJul 2022View details →
zenodo36/100

Data collected by citizen scientists reveal the role of climate and phylogeny on the frequency of shelter types used by frogs across the Americas

<p><strong>Supplementary Material </strong>&nbsp;of the manuscript on frog shelters across americas. Raw data and figures.</p> <p><strong>Table S1.</strong> The number of all anuran observations per species per country in the iNaturalist dataset on July 1, 2021.</p> <p><strong>Table S2.</strong> Distribution of shelter types among frog species retrieved from the iNaturalist platform across the Americas. Species with shelter first time reports are marked with *, shelter types are: AH = Holes in an artificial material; AS = Artificial surface; HG = Hole in the ground; HR = Among rocks; VBa = Hollow in bamboo; VBr = Bromelias or bromelia-like plants; VL = Live vegetation; VT = Tree trunk; VD = Leaf litter; WA = Water</p> <p><strong>Table S3.</strong> Anuran shelter sites around the world based on our literature review. *indicates the reference is secondary literature</p>

opencc-by-4.0Jul 2022View details →
dryad36/100

Evolutionary rates and shape variation along the anuran vertebral column with attention to phylogeny, body size, and ecology

<p><span>The vertebral column is critical to a vertebrate species' flexibility and skeletal support, making vertebrae a clear target for selection. Anur</span><span>ans (frogs and toads) have a unique, truncated vertebral column that appears constrained to provide axial rigidity for efficient jumping. However, no study has examined how presacral vertebrae shape varies among anuran species at the macroevolutionary scale nor how intrinsic (developmental and phylogenetic) and extrinsic (ecological) factors may have influenced vertebrae shape evolution. We used microCT scans and phylogenetic comparative methods to examine the vertebrae of hundreds of anuran species that vary in body size as well as adult and larval ecology. We found variation in shape and evolutionary rates among anuran vertebrae, dispelling any notion that trunk vertebrae evolve uniformly. We discovered the highest evolutionary rates in the cervical vertebrae and in the more caudal trunk vertebrae. We found little evidence for selection pressures related to adult or larval ecology affecting vertebrae evolution, but we did find body size was highly associated with vertebrae shape and microhabitat (mainly burrowing) affected those allometric relationships. Our results provide an interesting comparison to vertebrae evolution in other clades and a jumping-off point for studies of anuran vertebrae evolution and development.</span></p>

opencc-zeroAug 2022View details →
dryad36/100

Phylogenies related to: Codiversification of gut microbiota with humans

<p><span>The gut microbiomes of human populations worldwide have many core microbial species in common. However, within a species, some strains can show remarkable population specificity. The question is whether such specificity arises from a shared evolutionary history (codiversification) between humans and their microbes. To test for codiversification of host and microbiota, we analyzed paired gut metagenomes and human genomes for 1225 individuals in Europe, Asia, and Africa, including mothers and their children.  Between and within countries, signals of codiversification were evident for humans and their gut microbes. Moreover, species displaying the strongest codiversification independently evolved traits characteristic of host dependency, including reduced genomes, and oxygen and temperature sensitivity. These findings all point to the importance of understanding the potential role of population-specific microbial strains in microbiome-mediated disease phenotypes.</span></p>

opencc-zeroSep 2022View details →
dryad36/100

Data from: Resolution, conflict and rate shifts: Insights from a densely sampled plastome phylogeny for Rhododendron (Ericaceae)

<p><strong>Background and Aims</strong> <em>Rhododendron </em>is a species-rich and taxonomically challenging genus due to recent adaptive radiation and frequent hybridization. A well-resolved phylogenetic tree would help to understand the diverse history of <em>Rhododendron </em>in the Himalaya–Hengduan Mountains where the genus is most diverse.</p> <p><strong>Methods </strong>We reconstructed the phylogeny based on plastid genomes with broad taxon sampling, covering 161 species representing all eight subgenera and all 12 sections, including ~45 % of the <em>Rhododendron </em>species native to the Himalaya–Hengduan Mountains. We compared this phylogeny with nuclear phylogenies to elucidate reticulate evolutionary events and clarify relationships at all levels within the genus. We also estimated the timing and diversification history of <em>Rhododendron</em>, especially the two species-rich subgenera <em>Rhododendron</em> and <em>Hymenanthes </em>that comprise &gt;90 % of <em>Rhododendron </em>species in the Himalaya–Hengduan Mountains.</p> <p><strong>Key Results </strong>The full plastid dataset produced a well-resolved and supported phylogeny of <em>Rhododendron</em>. We identified 13 clades that were almost always monophyletic across all published phylogenies. The conflicts between nuclear and plastid phylogenies strongly suggested that reticulation events may have occurred in the deep lineage history of the genus. Within <em>Rhododendron</em>, subgenus <em>Therorhodion </em>diverged first at 56 Mya, then a burst of diversification occurred from 23.8 to 17.6 Mya, generating ten lineages among the component 12 clades of core <em>Rhododendron</em>. Diversification in subgenus <em>Rhododendron </em>accelerated c. 16.6 Mya and then became fairly continuous. Conversely, <em>Hymenanthes </em>diversification was slow at first, then accelerated very rapidly around 5 Mya. In the Himalaya–Hengduan Mountains, subgenus <em>Rhododendron </em>contained one major clade adapted to high altitudes and another to low altitudes, whereas most clades in <em>Hymenanthes </em>contained both low- and high-altitude species, indicating greater ecological plasticity during its diversification.</p> <p><strong>Conclusions </strong>The 13 clades proposed here may help to identify specific ancient hybridization events. This study will help to establish a stable and reliable taxonomic framework for <em>Rhododendron</em>, and provides insight into what drove its diversification and ecological adaption. Denser sampling of taxa, examining both organelle and nuclear genomes, is needed to better understand the divergence and diversification history of <em>Rhododendron</em>.</p>

opencc-zeroOct 2022View details →
dryad36/100

The phylogeny of Errazurizia (Fabaceae: Amorpheae) and description of the new monotypic genus Pictarena

<p><em>Errazurizia</em> (Fabaceae) is a genus comprised of four species of New World desert shrubs with an ambiguous evolutionary history. Prior studies determined the North American species of Errazurizia were polyphyletic and the relationship of <em>E</em>. <em>rotundata</em> with other genera in the tribe Amorpheae remained undetermined. The sole South American species, which is also the type species, has never been included in a molecular study. We inferred the phylogenetic relationships of <em>Errazurizia</em> and six closely related genera using data from the cpDNA genome and nrDNA cistron from reference-guided assemblies. Maximum likelihood and Bayesian analyses found two of the North American and the South American species were a monophyletic group, but that <em>E</em>. <em>rotundata</em> was sister to the monotypic genus <em>Parryella</em>. Gland and pollen surface characters confirm the close relationship between <em>P</em>. <em>filifolia</em> and <em>E</em>. <em>rotundata</em>. Cytonuclear discordance yielded partially incongruent tree topologies, and while the cpDNA phylogeny indicated a monophyletic Amorpha was sister to the <em>E</em>. <em>rotundata</em> and <em>P</em>. <em>filifolia</em> clade, the nrDNA cistron phylogeny recovered a paraphyletic <em>Amorpha</em>, with <em>A</em>. <em>californica</em> sister to the <em>E</em>. <em>rotundata</em> and <em>P</em>. <em>filifolia</em> clade. Molecular and morphological evidence support the elevation of <em>E</em>. <em>rotundata</em> to its own monotypic genus, <em>Pictarena</em>. The new genus <em>Pictarena</em> is defined by subsessile, suborbicular leaflets, mammiform leaflet glands, spicate inflorescences, and flowers with either all petals absent or rarely with a banner petal. Elevating <em>E</em>. <em>rotundata</em> to <em>Pictarena</em> resolves the confusing classification of the species, an imperiled endemic known only from four localities in northern Arizona and lends support for continued conservation.</p>

opencc-zeroOct 2022View details →
dryad36/100

Molecular phylogeny of Dermestidae (Coleoptera) reveals the polyphyletic nature of Trogoderma Latreille, and the taxonomic placement of the Khapra Beetle Trogoderma granarium Everts

<p>The hide, larder and carpet beetles (Coleoptera: Dermestidae) are a family of mainly scavenger beetles, with numerous species such as the khapra beetle (<em>Trogoderma</em> <em>granarium</em> Everts, 1898), the black carpet beetle (<em>Attagenus</em> <em>unicolor</em> (Brahm, 1791)) and the hide beetle (<em>Dermestes</em> <em>maculatus</em> De Geer, 1774) being widely recognised as serious economic pests of stored products and museum collections (Fig. 1). A stable classification and reliable identification of genera and species of these pests and their 1,700 relatives are of great relevance for trade restrictions, biosecurity, pest management, forensics and biodiversity surveys.</p> <p>In this study, we examined and sequenced mitochondrial genomes of 477 dermestid specimens, representing all subfamilies and 90% of the globally recognised tribes and subtribes. Our study provides the most comprehensive, taxonomically verified and vouchered resource of mitochondrial reference sequences linked to specimen images and occurrence records of pests and their relatives, enabling eDNA surveys, metabarcoding and molecular species identification. It also reconstructs the phylogeny of Dermestidae based on molecular and morphological data for the first time, thereby providing robust phylogenetic hypotheses for a stable classification system from family to genus-level.</p> <p>Accordingly, a revised classification of Dermestidae with formal nomenclatural changes is proposed, recognising six subfamilies: Orphilinae, Trinodinae, Trogoparvinae subfam. nov. (type genus <em>Trogoparvus</em> Háva, 2001), Dermestinae, Attageninae and Megatominae. Trinodinae is recovered towards the base of Dermestidae with three tribes: Trinodini (=Trinoparvini syn. nov.), Thylodriini and Trichelodini. Dermestinae is the only subfamily with adults lacking a median ocellus, and it includes the tribes Thorictini stat. nov. (that is downgraded from Thorictinae), Marioutini and Dermestini. The endemic Australian genus <em>Derbyana</em> Lawrence and Ślipiński, was recovered within Holarctic <em>Dermestes</em> Linnaeus. Attageninae is strongly supported and includes the monogeneric Adelaidiini and polygenic Attagenini. Former subgenera of <em>Attagenus</em> Latreille, i.e., <em>Lanorus</em> Mulsant and Rey (= Paranovelsis Casey syn. nov.), <em>Telopes</em> Redtenbacher, and <em>Aethriostoma</em> Motschulsky, are elevated to generic level. The largest clade, Megatominae, is confirmed as monophyletic and is divided into three tribes: Anthrenini, Ctesiini and Megatomini. Megatomini is divided into three subtribes: Megatomina, Orphinina subtribe nov. (type genus <em>Orphinus</em> Motschulsky) and Trogodermina. Within the economically important lineage Trogodermina, <em>Trogoderma</em> Latreille, is delimited to contain only Holarctic species including the Khapra beetle <em>T</em>. <em>granarium</em> Everts, while a Southern Hemisphere clade is here recognised as <em>Eurhopalus</em> Solier in Gay, 1849 (= <em>Anthrenocerus</em> Arrow, 1915; <em>Myrmeanthrenus</em> Armstrong, 1945; <em>Neoanthrenus</em> Armstrong, 1941; <em>Sodaliatoma</em> Háva, 2013; <em>Reesa</em> Beal, 1967 syn. nov.). A revised classification of the extant genera of Dermestidae is also provided.</p>

opencc-zeroOct 2022View details →
zenodo36/100

Multiple origin of the Phaenonotum beetles in the Greater Antilles (Coleoptera: Hydrophilidae): phylogeny, biogeography and systematics

<p>The systematics and the phylogenetic position of the Caribbean representatives of <em>Phaenonotum</em> Sharp (Coleoptera: Hydrophilidae) are investigated in order to understand the composition of the Caribbean fauna and its origin. Phylogenetic analysis based on mitochondrial and nuclear genes has revealed the Caribbean species to be situated in three deeply nested clades, inferring multiple colonization of Caribbean islands from the continent. Time-tree analysis and BioGeoBEARS analyses of ancestral ranges estimated the oldest clade, consisting of wingless single-island endemics of Cuba (<em>P. delgadoi</em>), Jamaica (<em>P. ondreji</em> <strong>sp. nov.</strong>) and Hispaniola (<em>P. laterale</em> <strong>sp. nov.</strong>), to have diverged ca. 46.6 Ma from the South American ancestor and subsequently colonizing the Caribbean most likely via the GAARlandia land bridge connecting South America with Greater Antilles. The remaining three Caribbean species, including the Puerto Rican endemic, <em>P. borinquenum</em> <strong>sp. nov.</strong>, are of more recent (Miocene to Pliocene) origin and colonized the Greater Antilles by over-water dispersal. All the Caribbean species are illustrated and diagnosed and three new species are described. The genus <em>Phaenonotum</em>, excluding <em>P. caribense</em> Archangelsky, is confirmed as a monophylum. We demonstrate that species-level taxonomy of <em>Phaenonotum</em> is difficult to solve by morphology alone, and ideally requires the combination of morphology and molecular markers.</p>

opencc-by-4.0Aug 2017View details →
zenodo36/100

Supplementary figures and data for "Complete phylogeny of Micrathena spiders suggests multiple dispersal events among Neotropical rainforests, islands, and landmasses, and indicates Andean orogeny promotes speciation"

<p>Supplementary figures and data for "Complete phylogeny of <em>Micrathena</em> spiders suggests multiple dispersal events among Neotropical rainforests, islands, and landmasses, and indicates Andean orogeny promotes speciation" by Ivan L. F. Magalhaes, Pedro H. Martins, B&aacute;rbara T. Faleiro, Teof&acirc;nia H. D. A. Vidigal, Fabr&iacute;cio R. Santos, Leonardo S. Carvalho, Adalberto J. Santos, submitted to <em>Cladistics</em>.&nbsp;</p> <p>Supplementary Figures S1 &ndash; S15</p> <p>Supplementary data S16: Complete specimen data of specimens used as vouchers for morphological scorings in Excel spreadsheet format.<br>Supplementary data S17: Discrete character matrix with morphological scorings in Nexus format.<br>Supplementary data S18: Complete specimen data of specimens used as vouchers for DNA sequencing in Excel spreadsheet format.<br>Supplementary data S19: Alignment of cytochrome oxidase I sequences in Fasta format.<br>Supplementary data S20: Alignment of histone H3 sequences in Fasta format.<br>Supplementary data S21: Alignment of 28S ribosomal sequences in Fasta format.<br>Supplementary data S22: Alignment of internal transcribed spacer sequences in Fasta format.<br>Supplementary data S23: Alignment of 16S ribosomal sequences in Fasta format.<br>Supplementary data S24: Zipped folder containing the inputs for estimating the phylogeny using morphological data in IQ-Tree: matrix in nexus format, partition file, and command file in plain text.<br>Supplementary data S25: Zipped folder containing the inputs for estimating the phylogeny using sequence data aligned with Muscle in IQ-Tree: matrix in nexus format, partition file, and command file in plain text.<br>Supplementary data S26: Zipped folder containing the inputs for estimating the phylogeny using sequence data aligned with MAFFT in IQ-Tree: matrix in nexus format, partition file, and command file in plain text.<br>Supplementary data S27: Zipped folder containing the inputs for estimating the phylogeny using morphological and sequence data aligned with MUSCLE in IQ-Tree: matrix in nexus format, partition file, and command file in plain text.<br>Supplementary data S28: Input Nexus for estimating the phylogeny using morphological data in MrBayes.<br>Supplementary data S29: Input Nexus for estimating the phylogeny using sequence data aligned with Muscle in MrBayes.<br>Supplementary data S30: Input Nexus for estimating the phylogeny using sequence data aligned with MAFFT in MrBayes.<br>Supplementary data S31: Input Nexus for estimating the phylogeny using morphological and sequence data aligned with Muscle in MrBayes.<br>Supplementary data S32: Input XML for estimating the dated phylogeny under Bayesian inference in BEAST.<br>Supplementary data S33: Distribution maps for all Micrathena species included in this study, the database with the original records and their source, and the R script used to generate the maps.<br>Supplementary data S34: Zipped folder containing all the inputs for estimating ancestral ranges and performing biogeographic stochastic mapping in R. This contains (0) the scripts for performing model selection and estimating ancestral states over a distribution of posterior trees, followed by stochastic mapping; (1) the geography and tree files (MMCT, and 100 trees randomly drawn from the posterior distribution); &nbsp;(2) the dispersal matrix and (3) the files for performing the time-stratified analysis to test the influence of the closure of the Isthmus of Panama on Micrathena dispersal.<br>Supplementary data S35: R script for generating the in-situ-speciation-through-time graphs from the results of biogeographic stochastic maps, as seen in Fig. 5.<br>Supplementary data S36: R script for getting and plotting elevations from individual records of Micrathena.<br>Supplementary data S37: R script for performing the GeoHiSSE estimation of net diversification rates among areas.<br>Supplementary data S38: Zipped folder containing the optimal trees found as a result of analysing inputs S24&ndash;S32 (IQ-Tree, MrBayes and BEAST).<br>Supplementary data S39: Zipped folder containing the ancestral range estimation results under competing models in BioGeoBEARS.<br>Supplementary data S40: Excel spreadsheet with parameter values of competing biogeographic models in BioGeoBEARS.<br>Supplementary data S41: Excel spreadsheet with results of biogeographic stochastic mapping over 100 different trees from the posterior distribution; includes all Micrathena species.<br>Supplementary data S42: Excel spreadsheet with results of biogeographic stochastic mapping over 100 different trees from the posterior distribution; includes only Micrathena species which had their DNA sequenced.<br>Supplementary data S43: Excel spreadsheet with the geography matrix, indicating which Micrathena species may be found in each area, and indicating the proportion of species from each area that are missing from the incomplete dataset &nbsp;(i.e., excluding species with unavailable DNA sequences).<br>Supplementary data S44: Excel spreadsheet with parameter values of competing biogeographic models estimated in GeoHiSSE.</p>

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