Options
Bradler, Sven
Loading...
Preferred name
Bradler, Sven
Official Name
Bradler, Sven
Alternative Name
Bradler, S.
Main Affiliation
Now showing 1 - 10 of 35
2014Journal Article [["dc.bibliographiccitation.firstpage","205"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Systematic Entomology"],["dc.bibliographiccitation.lastpage","222"],["dc.bibliographiccitation.volume","39"],["dc.contributor.author","Bradler, Sven"],["dc.contributor.author","Robertson, James A."],["dc.contributor.author","Whiting, Michael F."],["dc.date.accessioned","2018-11-07T09:42:17Z"],["dc.date.available","2018-11-07T09:42:17Z"],["dc.date.issued","2014"],["dc.description.abstract","The phasmatodeans or stick and leaf insects are considered to be a mesodiverse insect order with more than 3000 species reported mainly from the tropics. The stick insect subfamily Necrosciinae comprises approximately 700 described species in more than 60 genera from the Oriental and Australian region, forming the most species-rich subfamily traditionally recognized within Phasmatodea. However, the monophyly of this taxon has never been thoroughly tested and the evolutionary relationships among its members are unknown. We analyse three nuclear (18S and 28S rDNA, histone 3) and three mitochondrial (CO II, 12S and 16S rDNA) genes to infer the phylogeny of 60 species of stick insects that represent all recognized families and major subfamilies sensu Gunther and the remarkable diversity within Necrosciinae. Maximum parsimony, maximum likelihood and Bayesian techniques largely recover the same substantial clades, albeit with highly discordant relationships between them. Most members of the subfamily Necrosciinae form a clade. However, the genus Neohirasea-currently classified within Lonchodinae-is strongly supported as subordinate to Necrosciinae, whereas Baculofractum, currently classified within Necrosciinae, is strongly supported within Lonchodinae. Accordingly, we formally transfer Neohirasea and allied taxa (namely Neohiraseini) to Necrosciinae sensu nova (s.n.) and Baculofractum to Lonchodinae s.n. We also provide further evidence that Leprocaulinus, until recently recognized as Necrosciinae, belongs to Lonchodinae, and forms the sister taxon of Baculofractum. Furthermore, Lonchodinae is paraphyletic under exclusion of Eurycantha and Neopromachus. We reinstate the traditional view that Neopromachus and related taxa (Neopromachini sensu Gunther) are a subgroup of Lonchodinae and transfer those taxa + the New Guinean Eurycanthinae accordingly. Morphological evidence largely corroborates our molecular-based findings and also reveals that Menexenus fruhstorferi is a member of the genus Neohirasea and is thus transferred from Menexenus (Lonchodinae) to Neohirasea, as Neohirasea fruhstorferi comb.n. (Necrosciinae s.n.). Other phylogenetic results include Areolatae and Anareolatae each supported as polyphyletic, Heteropteryginae and Lanceocercata (Bayesian analysis) are monophyletic, albeit with low support, and Necrosciinae s.n. and Lonchodinae s.n. are recovered as sister taxa (Bayesian analysis)."],["dc.identifier.doi","10.1111/syen.12055"],["dc.identifier.isi","000332599700002"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/33922"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell"],["dc.relation.issn","1365-3113"],["dc.relation.issn","0307-6970"],["dc.title","A molecular phylogeny of Phasmatodea with emphasis on Necrosciinae, the most species-rich subfamily of stick insects"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2022-05-12Journal Article Research Paper [["dc.bibliographiccitation.artnumber","62"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","BMC Ecology and Evolution"],["dc.bibliographiccitation.volume","22"],["dc.contributor.author","Bank, Sarah"],["dc.contributor.author","Bradler, Sven"],["dc.date.accessioned","2022-06-01T09:39:41Z"],["dc.date.accessioned","2022-08-12T14:06:34Z"],["dc.date.available","2022-06-01T09:39:41Z"],["dc.date.available","2022-08-12T14:06:34Z"],["dc.date.issued","2022-05-12"],["dc.date.updated","2022-07-29T12:00:30Z"],["dc.description.abstract","Background\r\n The re-evolution of complex characters is generally considered impossible, yet, studies of recent years have provided several examples of phenotypic reversals shown to violate Dollo’s law. Along these lines, the regain of wings in stick and leaf insects (Phasmatodea) was hypothesised to have occurred several times independently after an ancestral loss, a scenario controversially discussed among evolutionary biologists due to overestimation of the potential for trait reacquisition as well as to the lack of taxonomic data.\r\n \r\n \r\n Results\r\n We revisited the recovery of wings by reconstructing a phylogeny based on a comprehensive taxon sample of over 500 representative phasmatodean species to infer the evolutionary history of wings. We additionally explored the presence of ocelli, the photoreceptive organs used for flight stabilisation in winged insects, which might provide further information for interpreting flight evolution. Our findings support an ancestral loss of wings and that the ancestors of most major lineages were wingless. While the evolution of ocelli was estimated to be dependent on the presence of (fully-developed) wings, ocelli are nevertheless absent in the majority of all examined winged species and only appear in the members of few subordinate clades, albeit winged and volant taxa are found in every euphasmatodean lineage.\r\n \r\n \r\n Conclusion\r\n In this study, we explored the evolutionary history of wings in Phasmatodea and demonstrate that the disjunct distribution of ocelli substantiates the hypothesis on their regain and thus on trait reacquisition in general. Evidence from the fossil record as well as future studies focussing on the underlying genetic mechanisms are needed to validate our findings and to further assess the evolutionary process of phenotypic reversals."],["dc.description.sponsorship"," Deutsche Forschungsgemeinschaft"],["dc.description.sponsorship"," Georg-August-Universität Göttingen"],["dc.description.sponsorship","Open-Access-Publikationsfonds 2022"],["dc.identifier.citation","BMC Ecology and Evolution. 2022 May 12;22(1):62"],["dc.identifier.doi","10.1186/s12862-022-02018-5"],["dc.identifier.pii","2018"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/108534"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/112726"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-572"],["dc.relation.eissn","2730-7182"],["dc.rights","CC BY 4.0"],["dc.rights.holder","The Author(s)"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","A second view on the evolution of flight in stick and leaf insects (Phasmatodea)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]Details DOI2014Journal Article [["dc.bibliographiccitation.artnumber","e91290"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","PLoS ONE"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Wang, L."],["dc.contributor.author","Bethoux, Olivier"],["dc.contributor.author","Bradler, Sven"],["dc.contributor.author","Jacques, Frederic M. B."],["dc.contributor.author","Cui, Yingying"],["dc.contributor.author","Ren, Dong"],["dc.date.accessioned","2018-11-07T09:42:29Z"],["dc.date.available","2018-11-07T09:42:29Z"],["dc.date.issued","2014"],["dc.description.abstract","Background: Fossil species that can be conclusively identified as stem-relatives of stick- and leaf-insects (Phasmatodea) are extremely rare, especially for the Mesozoic era. This dearth in the paleontological record makes assessments on the origin and age of the group problematic and impedes investigations of evolutionary key aspects, such as wing development, sexual size dimorphism and plant mimicry. Methodology/Principal Findings: A new fossil insect species, Cretophasmomima melanogramma Wang, Bethoux and Ren sp. nov., is described on the basis of one female and two male specimens recovered from the Yixian Formation (Early Cretaceous, ca. 126 +/- 4 mya; Inner Mongolia, NE China; known as 'Jehol biota'). The occurrence of a female abdominal operculum and of a characteristic 'shoulder pad' in the forewing allows for the interpretation of a true stem-Phasmatodea. In contrast to the situation in extant forms, sexual size dimorphism is only weakly female-biased in this species. The peculiar wing coloration, viz. dark longitudinal veins, suggests that the leaf-shaped plant organ from the contemporaneous 'gymnosperm' Membranifolia admirabilis was used as model for crypsis. Conclusions/Significance: As early as in the Early Cretaceous, some stem-Phasmatodea achieved effective leaf mimicry, although additional refinements characteristic of recent forms, such as curved fore femora, were still lacking. The diversification of small-sized arboreal insectivore birds and mammals might have triggered the acquisition of such primary defenses."],["dc.identifier.doi","10.1371/journal.pone.0091290"],["dc.identifier.isi","000333348500027"],["dc.identifier.pmid","24646906"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10033"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/33965"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Public Library Science"],["dc.relation.issn","1932-6203"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Under Cover at Pre-Angiosperm Times: A Cloaked Phasmatodean Insect from the Early Cretaceous Jehol Biota"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2018Journal Article [["dc.bibliographiccitation.journal","Frontiers in Ecology and Evolution"],["dc.bibliographiccitation.volume","6"],["dc.contributor.author","Büscher, Thies H."],["dc.contributor.author","Buckley, Thomas R."],["dc.contributor.author","Grohmann, Constanze"],["dc.contributor.author","Gorb, Stanislav N."],["dc.contributor.author","Bradler, Sven"],["dc.date.accessioned","2019-03-19T17:07:58Z"],["dc.date.available","2019-03-19T17:07:58Z"],["dc.date.issued","2018"],["dc.description.abstract","Insects have developed specialized structures on their feet for adhering to surfaces, with stick and leaf insects or Phasmatodea exhibiting an unexpectedly high diversity of these structures. In Phasmatodea, attachment on different substrates is achieved by two types of pads on the legs: the euplantulae on the tarsomeres and the arolium on the pretarsus. The euplantulae are adhesive structures capable of adaptability to the substrate profile and generation of the required attachment strength. The diversity of euplantular microstructures of 56 species that represent all major lineages recognized within Phasmatodea and the whole biogeographical distribution of the group are examined using scanning electron microscopy (SEM). Nine different types of attachment structures can be distinguished whereby one, the nubby type, can be further divided into three different distinct types based on the specific ratio of each conical outgrowth. We mapped the morphological data from the SEM onto a phylogenetic tree we reconstructed based on molecular data. Previously, the evolution of different adhesive microstructures (AMs) on these pads has been suggested to reflect phylogenetic groups. However, different types of AMs are found within monophyletic groups, and our ancestral character state reconstruction suggests smooth euplantulae in the ground pattern of Euphasmatodea and multiple independent origins of other forms. The type of AM appears to be strongly associated with ecomorphs, e.g., smooth euplantular surfaces are more frequently found in tree-dwellers than in ground-dwellers, whilst the attachment pads of ground-dwelling species primarily bear conical cuticular outgrowths (nubby euplantulae)."],["dc.identifier.doi","10.3389/fevo.2018.00069"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/57680"],["dc.language.iso","en"],["dc.notes.intern","DeepGreen Import"],["dc.publisher","Frontiers Media S.A."],["dc.relation.eissn","2296-701X"],["dc.rights","http://creativecommons.org/licenses/by/4.0/"],["dc.title","The Evolution of Tarsal Adhesive Microstructures in Stick and Leaf Insects (Phasmatodea)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2006Journal Article [["dc.bibliographiccitation.firstpage","171"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Organisms Diversity & Evolution"],["dc.bibliographiccitation.lastpage","184"],["dc.bibliographiccitation.volume","6"],["dc.contributor.author","Klug, Rebecca"],["dc.contributor.author","Bradler, Sven"],["dc.date.accessioned","2018-11-07T10:40:20Z"],["dc.date.available","2018-11-07T10:40:20Z"],["dc.date.issued","2006"],["dc.description.abstract","Recently several conflicting hypotheses concerning the basal phylogenetic relationships within the Phasmatodea (stick and leaf insects) have emerged. In previous studies, musculature of the abdomen proved to be quite informative for identifying basal taxa among Phasmatodea, and led to conclusions regarding the basal splitting events within the group. However, this character complex was not studied thoroughly for a representative number of species, and usually muscle innervation was omitted. In the present study the musculature and nerve topography of mid-abdominal segments in both sexes of seven phasmid species are described and compared in detail for the first time including all putative basal taxa, e.g. members of Timema, Agathemera, Phyllimae, Aschiphasmatinae and Heteropteryginae. The ground pattern of the muscle and nerve arrangement of mid-abdominal segments, i.e. of those not modified due to association with the thorax or genitalia, is reconstructed. In Timema, the inner ventral longitudinal muscles are present, whereas they are lost in all remaining Phasmatodea (Euphasmatodea). The ventral longitudinal muscles in the abdomen of Agathemera, which span the whole length of each segment, do not represent the plesiomorphic condition as previously assumed, but might be a result of secondary elongation of the external ventral longitudinal muscles. Sexual dimorphism, common within the Phasmatodea, also applies to the muscle arrangement in the abdomen of some species. Only in the females of Haaniella dehaanii (Heteropteryginae) and Phyllium celebicum (Phylliinae) the ventral external longitudinal muscles are elongated and span the length of the whole segment, possibly as a result of convergent evolution. (c) 2006 Gesellschaft fur Biologische Systematik. Published by Elsevier GrnbH. All rights reserved."],["dc.identifier.doi","10.1016/j.ode.2005.08.004"],["dc.identifier.isi","000240997500002"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/46280"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Gmbh, Urban & Fischer Verlag"],["dc.relation.issn","1439-6092"],["dc.title","The pregenital abdominal musculature in phasmids and its implications for the basal phylogeny of Phasmatodea (Insecta : Polyneoptera)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2012Journal Article [["dc.bibliographiccitation.firstpage","184"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Acta Zoologica"],["dc.bibliographiccitation.lastpage","199"],["dc.bibliographiccitation.volume","93"],["dc.contributor.author","Friedemann, Katrin"],["dc.contributor.author","Wipfler, Benjamin"],["dc.contributor.author","Bradler, Sven"],["dc.contributor.author","Beutel, Rolf Georg"],["dc.date.accessioned","2018-11-07T09:11:43Z"],["dc.date.available","2018-11-07T09:11:43Z"],["dc.date.issued","2012"],["dc.description.abstract","External and internal head structures of Phyllium siccifolium are described in detail. The findings are compared with conditions found in other phasmatodeans and members of other neopteran lineages. The compiled 125 characters were analysed cladistically. A clade Eukinolabia (Phasmatodea + Embioptera) was confirmed. Synapomorphies of these two taxa are the shift of the origin of M. tentorioparaglossalis to the hind margin of the prementum, the presence of M. tentorioscapalis medialis, and antennal muscles that originate exclusively on the anterior tentorial arms. Within Eukinolabia, the position of Timema remains somewhat ambiguous because of missing anatomical data. However, it was confirmed as sister group of Euphasmatodea in a monophyletic Phasmatodea. Apomorphic groundplan features of Euphasmatodea are salivary ducts with separate external openings, apically rounded glossae, the presence of the galealobulus, and the reduction of the antennifer. The monophyly of Neophasmatidae was confirmed. Autapomorphies are the loss ofM. frontobuccalis posterior, the anteriorly or dorsally directed maxillary palps, and the reduction of the mandibular incisivi. The analysis of characters of the head yielded three new autapomorphies of Phylliinae, the presence of a protuberance on the attachment site of the dorsal tentorial arms, dorsoventrally flattened maxillary-and labial palps, and possibly the narrow and U-shaped field of trichomes on the apical part of the galea."],["dc.identifier.doi","10.1111/j.1463-6395.2010.00497.x"],["dc.identifier.isi","000301484700005"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/26785"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell"],["dc.relation.issn","1463-6395"],["dc.relation.issn","0001-7272"],["dc.title","On the head morphology of Phyllium and the phylogenetic relationships of Phasmatodea (Insecta)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2011Journal Article [["dc.bibliographiccitation.firstpage","223"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Zoologischer Anzeiger - A Journal of Comparative Zoology"],["dc.bibliographiccitation.lastpage","245"],["dc.bibliographiccitation.volume","250"],["dc.contributor.author","Helm, Conrad"],["dc.contributor.author","Treulieb, Sarah"],["dc.contributor.author","Werler, Katrin"],["dc.contributor.author","Bradler, Sven"],["dc.contributor.author","Klass, Klaus-Dieter"],["dc.date.accessioned","2018-11-07T09:00:18Z"],["dc.date.available","2018-11-07T09:00:18Z"],["dc.date.issued","2011"],["dc.description.abstract","A detailed study of the exoskeleton and musculature of the phallic organ of Oxyartes lamellatus (Kirby, 1904) (Phasmatodea: Necrosciinae) is here presented - the first study of this kind for Phasmatodea. The asymmetrical phallic organ shows a highly complicated morphology, with several sclerites and many formative structural elements, of which a sclerotised bulb in the ejaculatory duct wall and a long flagellum arising from near it are among the most conspicuous. Four extrinsic and 20 intrinsic phallic muscles were found; many of these are quite compact bundles or sheets, while a few others are diffuse groups of fibres. Phallic morphology in Oxyartes is compared with the literature data on male genitalia in other Phasmatodea, but this is limited by the superficial treatment of phallic organs in the few relevant previous contributions. Yet, phallic organs appear as a useful new character system for phylogenetic reconstruction and species distinction in Phasmatodea. Comparison with phallic organs in other 'orthopteroid' insects shows that these organs are too different among orders as to allow for sound homologisation of phallic substructures. Consideration of development of phallic organs does not help in this aspect. There is no evidence of phasmatodean phallic organs being pedomorphic. (C) 2011 Elsevier GmbH. All rights reserved."],["dc.identifier.doi","10.1016/j.jcz.2011.04.005"],["dc.identifier.isi","000295894000005"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/24122"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Gmbh, Urban & Fischer Verlag"],["dc.relation.issn","0044-5231"],["dc.title","The male genitalia of Oxyartes lamellatus - phasmatodeans do have complex phallic organs (Insecta: Phasmatodea)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2020Journal Article [["dc.bibliographiccitation.firstpage","89"],["dc.bibliographiccitation.journal","ZooKeys"],["dc.bibliographiccitation.lastpage","126"],["dc.bibliographiccitation.volume","913"],["dc.contributor.author","Cumming, Royce T."],["dc.contributor.author","Bank, Sarah"],["dc.contributor.author","Le Tirant, Stephane"],["dc.contributor.author","Bradler, Sven"],["dc.date.accessioned","2020-12-10T18:47:39Z"],["dc.date.available","2020-12-10T18:47:39Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.3897/zookeys.913.49044"],["dc.identifier.eissn","1313-2970"],["dc.identifier.issn","1313-2989"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/17333"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/78839"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Notes on the leaf insects of the genus Phyllium of Sumatra and Java, Indonesia, including the description of two new species with purple coxae (Phasmatodea, Phylliidae)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI2018Journal Article [["dc.bibliographiccitation.journal","Frontiers in Ecology and Evolution"],["dc.bibliographiccitation.volume","6"],["dc.contributor.author","Robertson, James A."],["dc.contributor.author","Bradler, Sven"],["dc.contributor.author","Whiting, Michael F."],["dc.date.accessioned","2018-12-19T15:14:39Z"],["dc.date.available","2018-12-19T15:14:39Z"],["dc.date.issued","2018"],["dc.description.abstract","(Phasmatodea) are large, tropical, predominantly nocturnal herbivores, which exhibit extreme masquerade crypsis, whereby they morphologically and behaviorally resemble twigs, bark, lichen, moss, and leaves. Females employ a wide range of egg-laying techniques, largely corresponding to their ecological niche, including dropping or flicking eggs to the forest floor, gluing eggs to plant substrate, skewering eggs through leaves, ovipositing directly into the soil, or even producing a complex ootheca. Phasmids are the only insects with highly species-specific egg morphology across the entire order, with specific egg forms that correspond to oviposition technique. We investigate the temporal, biogeographic and phylogenetic pattern of evolution of egg-laying strategies in Phasmatodea. Our results unequivocally demonstrate that the ancestral oviposition strategy for female stick and leaf insects is to remain in the foliage and drop or flick eggs to the ground, a strategy that maintains their masquerade. Other major key innovations in the evolution of Phasmatodea include the (1) hardening of the egg capsule in Euphasmatodea; (2) the repeated evolution of capitulate eggs (which induce ant-mediated dispersal, or myrmecochory); (3) adapting to a ground or bark dwelling microhabitat with a corresponding shift in adult and egg phenotype and egg deposition directly into the soil; and (4) adhesion of eggs in a clade of Necrosciinae that led to subsequent diversification in oviposition modes and egg types. We infer 16 independent origins of a burying/inserting eggs into soil/crevices oviposition strategy, 7 origins of gluing eggs to substrate, and a single origin each of skewering eggs through leaves and producing an ootheca. We additionally discuss the systematic implications of our phylogenetic results. Aschiphasmatinae is strongly supported as the earliest diverging extant lineage of Euphasmatodea. Phylliinae and Diapheromerinae are both relatively early diverging euphasmatodean taxa. We formally transfer Otocrania from Cladomorphinae to Diapheromerinae and recognize two tribes within Diapheromerinae: Diapheromerini sensu nov. and Oreophoetini sensu nov. We formally recognize the clade comprising Necrosciinae and Lonchodinae as Lonchodidae stat. rev. sensu nov."],["dc.identifier.doi","10.3389/fevo.2018.00216"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/57143"],["dc.notes.status","zu prüfen"],["dc.title","Evolution of Oviposition Techniques in Stick and Leaf Insects (Phasmatodea)"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]Details DOI2015Journal Article [["dc.bibliographiccitation.firstpage","744"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","The Canadian Entomologist"],["dc.bibliographiccitation.lastpage","753"],["dc.bibliographiccitation.volume","147"],["dc.contributor.author","Archibald, S. Bruce"],["dc.contributor.author","Bradler, Sven"],["dc.date.accessioned","2018-11-07T09:48:42Z"],["dc.date.available","2018-11-07T09:48:42Z"],["dc.date.issued","2015"],["dc.description.abstract","Stem-group Phasmatodea, known as the Susumanioidea, are previously established from the Jurassic through the Paleocene. Here, we extend this record to the early Eocene with five new fossils: two forewings from the Klondike Mountain Formation exposures at Republic, Washington, United States of America, and three partially complete specimens from the McAbee locality in southern British Columbia, Canada. We assign both of the Republic specimens to the new genus and species Eoprephasma hichensi new genus, new species. Two of the McAbee fossils appear to represent two further new species, which we refer to as Susumanioidea species A and B for lack of clearly preserved diagnostic species-level character states. The third might belong to one of these two species, but this is unclear. In all three, the mesothorax and metathorax are not notably extended, the forewings are not shortened, the foreleg femur is straight, and species A possesses an extended, external ovipositor with an operculum (unknown in the other specimens). These conditions are rare and never found in combination in Euphasmatodea. All other stem-group Phasmatodea younger than the Early Cretaceous of China are only known from isolated wings."],["dc.identifier.doi","10.4039/tce.2015.2"],["dc.identifier.isi","000363282900011"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/35361"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Cambridge Univ Press"],["dc.relation.issn","1918-3240"],["dc.relation.issn","0008-347X"],["dc.title","Stem-group stick insects (Phasmatodea) in the early Eocene at McAbee, British Columbia, Canada, and Republic, Washington, United States of America"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS