Conservation efforts must be evidence-based, so rapid and economically feasible methods should be used to quantify diversity and distribution patterns. We have attempted to overcome current ...impediments to the gathering of biodiversity data by using integrative phylogenomic and three mtDNA fragment analyses. As a model, we sequenced the Metriorrhynchini beetle fauna, sampled from ~700 localities in three continents. The species-rich dataset included ~6500 terminals, ~ 1850 putative species delimited at 5% uncorrected pairwise threshold, possibly ~1000 of them unknown to science. Neither type of data could alone answer our questions on biodiversity and phylogeny. The phylogenomic backbone enabled the integrative delimitation of robustly defined natural genus-group units that will inform future research. Using constrained mtDNA analysis, we identified the spatial structure of species diversity, very high species-level endemism, and a biodiversity hotspot in New Guinea. We suggest that focused field research and subsequent laboratory and bioinformatic workflow steps would substantially accelerate the inventorying of any hyperdiverse tropical group with several thousand species. The outcome would be a scaffold for the incorporation of further data from environmental sequencing and ecological studies. The database of sequences could set a benchmark for the spatiotemporal evaluation of biodiversity, would support evidence-based conservation planning, and would provide a robust framework for systematic, biogeographic, and evolutionary studies.
The elateroid family Lycidae is known for limited dispersal propensity and high species-level endemism. The red net-winged beetle, Dictyoptera aurora (Herbst, 1874), differs from all relatives by the ...range comprising almost the entire Holarctic region. Based on a five-marker phylogeny and 67 barcode entries (cox1-5′ mtDNA) from the whole range, we recovered two genetically distinct species within traditionally defined D. aurora and resurrected the name D. coccinata (Say, 1835) as the oldest available synonym for Nearctic populations. Yet, no reliable morphological trait distinguishes these species except for minute differences in the male genitalia. D. coccinata is a monophylum resulting from a single Miocene dispersal event, ~15.8 million years ago, and genetic divergence implies long-term isolation by the Bering Strait. Far East Asian and west European populations are also genetically distinct, although to a lower extent. Two independent colonization events established the Fennoscandian populations after the last glacial maximum. Besides intrinsic factors, the high morphological similarity might result from stabilizing selection for shared aposematic signals. The rapidly accumulating barcode data provide valuable information on the evolutionary history and the origins of regional faunas.
Abstract
The Lycini (Elateroidea: Lycidae) contains > 400 species placed in four typologically based genera and numerous subgenera. We assembled a mito-ribosomal dataset representing ~100 species ...from the whole range and recovered a phylogeny rejecting Lycus and Lycostomus as polyphyletic assemblages. The male-specific wide elytra and elytral thorns are identified in unrelated Neolycus and Lycus. The morphological similarity based on sexual dimorphism and aposematic patterns defined terminal clades and misled the genus-rank classification. We delimit Neolycus, Rhyncheros reinst. name (= Thoracocalon syn. nov. = Lyconotus syn. nov.), LipernesLycostomus, Haplolycus and Lycus. Demosis and six subgenera of Lycus are synonymized with Lycus. Celiasis Laporte, 1840 is kept in the classification as a nomen dubium until any specimen is available. The deep lineages are known from the Americas and Asia. Africa was colonized by Lycus and Haplolycus. Each specific aposematic pattern occurs in a limited range, and the similar body shape and coloration evolved in unrelated sympatrically occurring lineages. High intraspecific polymorphism is putatively a result of the adaptation of various populations to local mimetic assemblages. Therefore, the delimitation of many phenotypically diverse species should be investigated.
We reviewed the species-level classification of Metriorrhynchina net-winged beetles to make the group accessible for further studies. Altogether, 876 valid species are listed in a checklist along ...with known synonyms, combinations, and distribution data. The compilation of geographic distribution showed that Metriorrhynchina is distributed mainly in the Australian region with very high diversity in the islands at the northern edge of the Australian craton, i.e., in the Moluccas and New Guinea (54 and 423 spp. respectively). The neighboring northern part of the Australian continent houses a majority of known Australian species (112 spp.) and the diversity of net-winged beetles gradually decreases to the south (43 spp.). The fauna of Sulawesi is highly endemic at the generic level (4 of 10 genera, 67 of 84 spp.). Less Metriorrhynchina occur in the Solomon Islands and Oceania (in total 22 spp.). The Oriental Metriorrhynchina fauna consists of a few genera and a limited number of species, and most of these are known from the Philippines (51 of 94 Oriental spp.). We identified a high species level turn-over between all neighboring landmasses. The genus-level endemism is high in Sulawesi (4 genera) and New Guinea (11 genera), but only a single genus is endemic to Australia. During the compilation of the checklist, we identified some homonyms, and we propose the following replacement names and a new synonym: Metriorrhynchus pseudobasalis, nom. nov. for M. basalis Lea, 1921 nec M. basalis Bourgeois, 1911; Metriorrhynchus pseudofunestus, nom. nov. for M. funestus Lea, 1921 nec M. funestus (Guérin-Méneville, 1838), Trichalus pseudoternatensis, nom. nov. for T. ternatensis Kleine, 1930 nec T. ternatensis Bourgeois, 1900, Procautires subparallelus, nom. nov. for P. parallelus (Pic, 1926) nec P. parallelus (Bourgeois, 1883), and Cautires pseudocorporaali, nom. nov. for C. corporaali (Pic, 1921: 12), (formerly Odontocerus and Cladophorus) nec C. corporaali (Pic, 1921) (formerly Bulenides, later Cautires). Diatrichalus biroi Kleine, 1943, syn. nov. is proposed as a junior subjective synonym of D. subarcuatithorax (Pic, 1926). Altogether, 161 new combinations are proposed, and 47 species earlier placed in Xylobanus Waterhouse, 1879 transferred from Cautirina to Metriorrhynchina incertae sedis. The study clarifies the taxonomy of Metriorrhynchini and should serve as a restarting point for further taxonomic, evolutionary, and biogeographic studies.
Dermestidae (Bostrichoidea) exploit diverse food sources including fungal mycelia, but notably they as saprophagous, feeding on decomposing and dried flesh and keratin of animals and plants. Some of ...them live in spider webs, vertebrate and social insect nests, while others cause damage in human dwellings. Here, we use mitogenomics to reconstruct their phylogeny and evolution of life history strategies. We recovered serial splits of Orphilinae, Thorictinae + Dermestinae, Attageninae, Trinodinae and Megatominae, and we dated the origins of all subfamilies between the Middle Jurassic and Upper Cretaceous. Extant genera started their diversification in the Middle Cretaceous, except for Dermestes that originated in the Eocene. Mycetophagy, the likely feeding style of the common ancestor with Endecatomidae, was retained only by Orphilinae. Since the Late Jurassic, most dermestids have been saprophagous with the preference for desiccated tissue. We infer a scenario of feeding preferences from mycetophagy moving to saprophagy, always depending on food with low water content, followed by the shift from cryptic life in crevices and wood, to commensalism with social Hymenoptera, and ultimately feeding on angiosperm pollen as adults. The dependence on spider larders evolved already in the Early Cretaceous, but lineages with this specialized strategy remained species‐poor. We date the origin of exploitation of vertebrate carcasses to the Eocene when modern mammalian fauna became dominant. The diversification of Megatominae (62% of known dermestids) and Attagenus Latreille (17%) coincides with the radiation of angiosperms.
Using mitogenomic phylogeny, we analysed relationships among dermestid subfamiles and dated the origins of major groups.
The dating analyses estimate the split of Dermestidae and Ptinidae + Bostrichidae to the Middle Triassic and the origins of major genera to the Middle Cretaceous.
Mycetophagy predisposes to saprophagy; flightlessness and host specificity drive diversification; free living in crevices precedes commensalism; and association with the angiosperms is important for groups living in arid ecosystems.
Abstract
Only 22 net-winged beetle species (Elateroidea: Lycidae) are known from the Western Palaearctic region (WPR), i.e. less than 0.5% of the global lycid diversity and much fewer than from ...similar latitudes of East Asia or Northern America. We used comprehensive distribution data and a molecular phylogeny of ~400 world lycids, including 14 European species, to provide a new perspective for understanding the structure and evolution of this group in the WPR. All Mediterranean species represent deeply rooted lineages with relatives in eastern Asia. These species occur in relictual ranges close to the family’s Pleistocene refugial edge. The phylogeny points to the loss of biological connection with East Asia since the Mid-Miocene. A third of WPR species is widespread in Central and Northern Europe, reaching eastern Asia, some of them possibly younger elements of the European fauna. Unlike the relatively high diversity in the Eocene amber, the extant net-winged beetles represent a small fraction of elateroid diversity in the WPR and are generally rare. Therefore, we assume that most WPR species are relics trapped in Mediterranean refugia since the onset of the Plio-Pleistocene cooling and are critically endangered by the ongoing loss of suitable habitats.
This study addresses the long-standing uncertainty about the internal classification of soldier beetles (Elateroidea: Cantharidae). Four datasets were compiled and analysed: 66 genes for 14 ...terminals, 15 mtDNA genes for 79 terminals, one mtDNA and two rRNA genes for 217 terminals, and barcodes for 576 terminals. Based on congruent topologies, Chauliognathinae is proposed as a sister to the remaining Cantharidae, followed by the redefined Malthininae (including Tytthonyxini), the paraphyletic "dysmorphocerine" lineages (Dysmorphocerinae sensu stricto and Heteromastiginae subfam. nov.), and Silinae + Cantharinae as a terminal clade. The present phylogeny supersedes earlier morphology and short-fragment molecular hypotheses that have not converged on a consensus. Few morphological characters corroborate the DNA-based relationships (see the adults and larval keys). However, morphology-based hypotheses have relied on a few informative characters, and no evidence strongly rejects the preferred molecular topology. The interpretation of morphological characters and uncertain polarity resulting from the high phenotypic disparity of Elateroidea are discussed in detail. The dated phylogeny hypothesizes the earliest split within the Cantharidae in the Berriasian stage (Early Cretaceous, ~141 Myr) and the diversification of most extant subfamilies and tribes already in the Late Cretaceous. The most diverse subfamily, Cantharinae, represents a delayed radiation that started during the Eocene climatic optimum, 55.5 Myr. The late origin of Cantharinae questions the classification of Cretaceous Cantharidae as members of Cantharinae. Instead, the results suggest their deeper rooting after separating from dysmorphocerine lineages and before the node between Cantharinae and Silinae.
We evaluated the red net-winged beetle populations’ morphological and genetic divergence within the Holarctic region. In contrast with relatives, D. aurora occurs in an exceptionally large range and ...very different ecosystems. In Northern America, we found an earlier undetected cryptic species isolated by the Bering Strait since the mid-Miocene. D. aurora colonized Fennoscandia from at least two refugia after the last glacial maximum. The absence of morphological differentiation is supposedly affected by the selection for similarity in the Müllerian mimicry ring. The results exemplify the phylogeographic history in the Holarctic region and contribute to understanding the morphological stasis in an extensive circumpolar range. The elateroid family Lycidae is known for limited dispersal propensity and high species-level endemism. The red net-winged beetle, Dictyoptera aurora (Herbst, 1874), differs from all relatives by the range comprising almost the entire Holarctic region. Based on a five-marker phylogeny and 67 barcode entries (cox1-5′ mtDNA) from the whole range, we recovered two genetically distinct species within traditionally defined D. aurora and resurrected the name D. coccinata (Say, 1835) as the oldest available synonym for Nearctic populations. Yet, no reliable morphological trait distinguishes these species except for minute differences in the male genitalia. D. coccinata is a monophylum resulting from a single Miocene dispersal event, ~15.8 million years ago, and genetic divergence implies long-term isolation by the Bering Strait. Far East Asian and west European populations are also genetically distinct, although to a lower extent. Two independent colonization events established the Fennoscandian populations after the last glacial maximum. Besides intrinsic factors, the high morphological similarity might result from stabilizing selection for shared aposematic signals. The rapidly accumulating barcode data provide valuable information on the evolutionary history and the origins of regional faunas.
Abstract
The Lycidae genera have seldom been tested with phylogenetic analyses. Therefore, we assembled genomic data to estimate the phylogenetic backbone of the porrostomines, one of ...Metriorrhynchina’s major clades. Further, mtDNA and morphology were employed to assign 352 analyzed species to genera. We present evidence for the paraphyly of Metriorrhynchus and terminal position of Porrostoma, revise the generic classification, and describe eight genera: Maraiakoreus gen. nov., Kuarhynchus gen. nov., Riedelrhynchus gen. nov., Bundikanus gen. nov., Yamarhynchus gen. nov., Bekorhynchus gen. nov., Sundarhynchus gen. nov., and Isuarhynchus gen. nov. We synonymize Stadenus Waterhouse, 1879, syn. nov., Metriorrhynchoides Kleine, 1923, syn. nov., and Oriomum Bocak, 1999a, syn. nov., to Porrostoma Castelnau, 1838. Next, we propose 75 new combinations and four new species: Bundikanus styskalai sp. nov., Kuarhynchus sisrangensis sp. nov., Maraiakoreus argenteus sp. nov., and Yamarhynchus sinopassensis sp. nov. We identified repeated origins of several external morphological traits earlier used to delimitate genera. Therefore, we prefer concordant evidence from the densely sampled mitochondrial phylogenies and male genitalia. The analyses identify high phylogenetic diversity and species richness in New Guinea, much lower phylogenetic diversity of the Australian continental fauna, and the limited permeability of the Wallacea that resulted in a single porrostomine genus in Asia. We point to the common acceptance of paraphyletic and polyphyletic taxa in the current classification. As a result, taxonomy has not provided expected support for any state-of-the-art evolutionary and zoogeographic studies. The phylogeny, species inventory, and classification of porrostomines set the basis for future evolutionary and zoogeographical studies.
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