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(2001). Animal behavior: An evolutionary approach (7th ed.). Sunderland: Sinauer Associates.\nAndrew, R. J., & Tembhare, D. B. (1992). Surface ultrastructure of the egg chorion in the dragonfly Ictinogomphus rapax (Rambur) (Odonata: Gomphidae). International Journal of Insect Morphology and Embryology, 21, 347–350.\nAndrew, R. J., Kodhe, L., & Kurup, S. S. (2006). Fine structural changes in the egg chorion of Bradinopyga geminata (Rambur) induced by paper mill effluent (Anisoptera: Libellulidae). Odonatologica, 35, 187–192.\nArnqvist, G., & Nilsson, T. (2000). The evolution of polyandry: multiple mating and female fitness in insects. Animal Behavior, 60, 145–164.\nBechly, G., Brauckmann, C., Zessin, W. & Gröning, E. (2001). New results concerning the morphology of the most ancient dragonflies (Insecta: Odonatoptera) from the Namurian of Hagen-Vorhalle (Germany). Journal of Zoological Systematics and Evolutionary Research, 39, 209–226. doi:10.1046\u002Fj.1439-0469.2001.00165.x.\nBechly, G. (2007). Phylogenetic systematics of Odonata. http:\u002F\u002Fwww.bernstein.naturkundemuseum-bw.de\u002Fodonata\u002Fsystem.htm. Accessed 12 June 2012.\nBeckemeyer, R. J. (2004). Notes on the behavior and mechanics of scooping oviposition in Libellula composita (Hagen) (Anisoptera: Libellulidae). Odonatologica, 33, 11–23.\nBennett, S., & Mill, P. J. (1995). Pre- and post-maturation survival in adults of the damselfly Pyrrhosoma nymphula (Zygoptera: Coenagrionidae). Journal of Zoology, 235, 559–575.\nBonduriansky, R. (2001). The evolution of male mate choice in insects: a synthesis of ideas and evidence. Biological Reviews, 76, 305–339.\nBuskirk, R. E., & Sherman, K. J. (1985). The influence of larval ecology on oviposition and mating strategies in dragonflies. Florida Entomologist, 68, 39–51.\nBybee, S. M., Ogden, T. H., Branham, M. A., & Whiting, M. F. (2008). Molecules, morphology and fossils: a comprehensive approach to odonate phylogeny and the evolution of the odonate wing. Cladistics, 23, 1–38.\nCarle, F. L., & Kjer, K. M. (2002). Phylogeny of Libellula Linnaeus (Odonata: Insecta). Zootaxa, 87, 1–18.\nCarle, F. L., Kjer, K. M., & May, M. L. (2008). Evolution of Odonata, with special reference to Coenagrionoidea (Zygoptera). Arthropod Systematics & Phylogeny, 66, 37–44.\nConrad, K. F., & Pritchard, G. (1992). An ecological classification of odonate mating systems: The relative influence of natural, inter– and intra–sexual selection on males. Biological Journal of the Linneaen Society, 45, 255–269.\nConvey, P. S. (1992). Predation risks associated with mating and oviposition for female Crocothemis erythraea (Brulle) (Anisoptera: Libellulidae). Odonatologica, 21, 343–350.\nCorbet, P. S. (1980). Biology of Odonata. Annual Review of Entomology, 25, 189–217.\nCorbet, P. S. (2004). Dragonflies: Behaviour and ecology of Odonata. Colchester: Harley.\nCordero Rivera, A., Andres, J. A., Cordoba-Aguilar, A., & Utzeri, C. (2004). Postmating sexual selection: allopatric evolution of sperm competition mechanisms and genital morphology in calopterygid damselflies (Insecta: Odonata). Evolution, 58, 349–359.\nCórdoba-Aguilar, A. (2008). Dragonflies and damselflies: Model organisms for ecological and evolutionary research. Oxford: Oxford University Press.\nDanielsson, I. (1998). Mechanisms of sperm competition in insects. Annales Zoologici Fennici, 35, 241–257.\nDumont, H. J., Vierstraete, A., & Vanfleteren, J. R. (2010). A molecular phylogeny of the Odonata (Insecta). Systematic Entomology, 35, 6–18.\nDunkle, S. W. (2000). Dragonflies through binoculars. New York: Oxford University Press.\nFelsenstein, J. (1985). Confidence limits on phylogenies: An approach using the bootstrap. Evolution, 39, 783–791.\nFincke, O. M. (1992). Interspecific competition for tree holes – consequences for mating systems and coexistence in neotropical damselflies. American Naturalist, 139, 80–101.\nFincke, O. M. (1997). Conflict resolution in the Odonata: Implications for understanding female mating patterns and female choice. Biological Journal of the Linneaen Society, 60, 201–220.\nFincke, O. M., Waage, J. K., & Koenig, W. (1997). Natural and sexual selection components of odonate mating patterns. In J. C. Choe & B. J. Crespi (Eds.), The evolution of mating systems in insects and arachnids (pp. 58–74). Cambridge: Cambridge University Press.\nFleck, G., Nel, A., Bechly, G., Delclos, X., Jarzembowski, A., & Coram, R. (2009). New Lower Cretaceous ‘libelluloid’ dragonflies (Insecta: Odonata: Cavilabiata) with notes about estimated divergence dates for this group. Palaeodiversity, 1, 19–36.\nGaino, E., Piersanti, S., & Rebora, M. (2008). Egg envelope synthesis and chorion modification after oviposition in the dragonfly Libellula depressa (Odonata, Libellulidae). Tissue & Cell, 40, 317–324.\nGrimaldi, D., & Engel, M. S. (2005). Evolution of the Insects. Cambridge: Cambridge University Press.\nGu, X., Fu, Y.-X., & Li, W.-H. (1995). Maximum likelihood estimation of the heterogeneity of substitution rate among nucleotide sites. Molecular Biology and Evolution, 12, 546.\nGuttell, R. R., Gray, M. W., & Schinare, M. N. (1993). A compilation of large subunit (23S and 23S-like) ribosomal RNA structures. Nucleic Acids Research, 21, 3055–3074.\nHassan, A. (1981). Coupling and oviposition behaviour in two macrodiplacinid libellulids Aethriamantha rezia (Kirby) and Urothemis assignata Selys (Libellulidae: Odonata). Zoological Journal of the Linnean Society, 72, 289–296.\nHopper, K. R. (1999). Risk-spreading and bet–hedging in insect population biology. Annual Review of Entomology, 44, 535–560.\nHuelsenbeck, J. P., & Ronquist, F. (2002). MrBayes 3: Bayesian analysis of phylogeny. University of California.\nHynes, H. B. N. (1970). The ecology of running waters. Toronto: University of Toronto Press.\nIshizawa, N. (2008). Factors in the selection of oviposition mode in Sympetrum infuscatum (Selys) (Anisoptera: Libellulidae). Odonatologica, 37, 317–328.\nJohansson, F., & Suhling, F. (2004). Behaviour and growth of dragonfly larvae along a permanent-temporary water habitat gradient. Ecological Entomology, 29, 196–202.\nKarlsson, M., Koch, K., & Sahlén, G. (2010). Ovariole numbers and stepwise oocyte production in Libellulidae (Odonata). Odonatologica, 39, 107–119.\nKennedy, C. H. (1922). The morphology of the penis in the genus Libellula. Entomological News, 33, 33–40.\nKisdi, E. (2002). Dispersal: risk spreading versus local adaptation. American Naturalist, 159, 579–595.\nKjer, K. M. (1995). Use of rRNA secondary structure in phylogenetic studies to identify homologous positions: an example of alignment and data presentation from the frogs. Molecular Phylogenetics and Evolution, 4, 314–330.\nKjer, K. M., Gillespie, J. J., & Ober, K. A. (2007). Opinions on multiple sequencealignment, and an empirical comparison of repeatability and accuracy between POY and structural alignments. Systematic Biology, 56, 133–146.\nKoch, K., & Suhling, F. (2005). Do behavioural and life-history traits vary with mate-guarding intensity in libellulid odonates? Canadian Journal of Zoology, 83, 1631–1637.\nKoch, K., Quast, M., & Sahlén, G. (2009). Morphological differences in the ovary of Libellulidae (Odonata). International Journal of Odonatology, 12, 147–156.\nKoch, K., Fuchs, N., & Sahlén, G. (2011). Morphology of follicle cells of Libellulidae (Odonata). International Journal of Odonatology, 14, 257–267.\nLetsch, H. (2007). Phylogeny of Anisoptera (Insecta: Odonata): promises and limitations of a new alignment approach. PhD Thesis. Universität Bonn.\nMaddison, W. P., & Maddison, D. R. (2011). Mesquite: a modular system for evolutionary analysis. Version 2.75. http:\u002F\u002Fmesquiteproject.org. Accessed 12 June 2012.\nMartens, A. (2003). Reproductive behaviour of African Odonata – a review. Cimbebasia, 18, 225–241.\nMatushkina, N. A. (2011). Morphology of exophytic ovipositors in dragonflies (Odonata: Gomphidae, Corduliidae, Libellulidae), with particular reference to ovipositor muscles and sensilla. International Journal of Odonatology, 14, 233–248.\nMatushkina, N. A., & Gorb, S. (2001). Stylus of the odonate endophytic ovipositor: a mechanosensory organ controlling egg positioning. Journal of Insect Physiology, 48, 213–219.\nMay, M. L. (1995). Comparative notes on micropyle structure in “cordulegastroid” and “libelluloid” Anisoptera. Odonatologica, 24, 53–62.\nMcPeek, M. A., & Peckarsky, B. L. (1998). Life histories and the strengths of species interactions: combining mortality, growth and fecundity effects. Ecology, 79, 235–247.\nMichiels, N. K., & Dhondt, A. A. (1991). Characteristics of dispersal in sexually mature dragonflies. Ecological Entomology, 16, 449–459.\nMiller, P. L. (1983). Contact guarding during oviposition in Hemianax ephippiger (Burmeister) and Anax parthenope (Selys) (Aeshnidae: Odonata). Tombo, 25, 17–19.\nMiller, P. L. (1991). Pre-tandem and in-tandem courtship in Libellulidae (Anisoptera). Advances in Odonatology, 5, 89–101.\nMiller, P. L., & Miller, A. K. (1985). Rates of oviposition and some other aspects of reproductive behaviour in Tholymis tillarga (Fabricius) in Kenya (Anisoptera: Libellulidae). Odonatologica, 14, 287–299.\nPeckarsky, B. L. (1983). Biotic interactions or abiotic limitations? A model of lotic community structure. In T. D. Fontaine III & S. M. Bartell (Eds.), Dynamics of lotic ecosystems (pp. 303–323). Ann Arbor: Ann Arbor Science Publications.\nPfau, H. K. (1971). Struktur und Funktion des sekundären Kopulationsapparates der Odonaten (Insecta, Palaeoptera), ihre Wandlung in der Stammesgeschichte und Bedeutung für die adaptive Entfaltung der Ordnung. Zeitschrift für Morphologie der Tiere, 70, 281–371.\nPfau, H. K. (1991). Contributions of functional morphology to the phylogenetic systematics of Odonata. Advances in Odonatolology, 5, 109–141.\nPfau, H. K. (2005). Structure, function and evolution of the ‘glans’ of the anisopteran vesica spermalis (Odonata). International Journal of Odonatology, 8, 259–310.\nPhilippi, T., & Seger, J. (1989). Hedging one's evolutionary bets, revisited. Trends in Ecology & Evolution, 4, 41–44.\nPilgrim, E. M., & von Dohlen, C. D. (2008). Phylogeny of the Sympetrinae (Odonata: Libellulidae): further evidence of the homoplasious nature of wing venation. Systematic Entomology, 33, 159–174.\nPosada, D. (2008). jModelTest: Phylogenetic model averaging. Molecular Biology and Evolution, 25, 1253–1256.\nRambaut, A., & Drummond, A. J. (2007). Tracer v1.4. http:\u002F\u002Fbeast.bio.ed.ac.uk\u002FTracer. Accessed 12 June 2012.\nRehfeldt, G. E. (1992). Aggregation during oviposition and predation risk in Sympetrum vulgatum L. (Odonata: Libellulidae). Behavioral Ecology and Sociobiology, 30, 317–322.\nRivera, A. C., Utzeri, C., & Carbone, S. S. (1999). Emergence and adult behaviour of Macromia splendens (Pictet) in Galicia, northwestern Spain (Anisoptera: Corduliidae). Odonatologica, 28, 333–342.\nRobertson, H. M. (1982). Courtship displays and mating behaviour of three species of Chlorocyphidae (Zygoptera). Odonatologica, 11, 53–58.\nSahlén, G. (1994a). Ultrastructure of the eggshell and micropylar apparatus of Somatochlora (Vander Lind.), Orthetrum cancellatum (L.) and Sympetrum sanguineum (Müll.) (Anisoptera: Corduliidae, Libellulidae). Odonatologica, 23, 255–269.\nSahlén, G. (1994b). Ultrastructure of the eggshell of Aeshna juncea (L.) 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Molecular Biology and Evolution, 11, 316–324.",{"EN":221},"In Libellulidae, oocyte production has been assumed to be continuous, with periods of egg-laying interspersed with periods of resting\u002Feating; however, recent work suggests that two types of oocyte production are common: either (a) continuous or (b) step-wise. These are mirrored in the arrangement of the ovarioles in the ovaries. Likewise, two types of mate-guarding behavior have been observed in Libellulidae: (1) non–contact guarding and (2) tandem guarding in which the male either hovers above the female or is physically attached to her during oviposition. Using molecular (mitochondrial and nuclear) data we explored the evolution of female reproductive traits, focusing on ovariole morphology, as well as guarding behavior, in Libellulidae. Continuous egg production appears to have evolved more than once, as have tandem and non-contact guarding. We discuss how the evolution of different ovariole types and guarding behavior may have been influenced by habitat instability, dispersal and crowded oviposition sites; thus, migratory behavior or habitat availability may have been the driving force of ovariole evolution.",{"EN":223},"Evolution of reproductive strategies in libellulid dragonflies (Odonata: 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USA",{},{"id":24,"sortIndex":102,"affiliation":244,"properties":24},{"id":245,"createTime":246,"updateTime":246,"relativeEntities":247,"slug":24,"properties":248,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"868e9cd9-ec00-4bc0-8122-eddf8640dcfd","2023-12-19T23:54:05.649+00:00",[],{"title":249},{"VI":250},"Department of Biology, Rutgers University, Newark, USA",{"title":252},{"VI":253},"Jessica Ware",{"id":255,"sortIndex":25,"researcher":24,"roles":256,"affiliations":257,"properties":266},"3ceab6b8-2dc1-44b2-8997-2952783fc256",[147],[258],{"id":24,"sortIndex":102,"affiliation":259,"properties":24},{"id":260,"createTime":261,"updateTime":261,"relativeEntities":262,"slug":24,"properties":263,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"f343a0ca-e0f0-456c-aace-835724bb82ae","2023-12-19T23:54:05.677+00:00",[],{"title":264},{"VI":265},"Department of Ecology, Johannes Gutenberg–University Mainz, Mainz, Germany",{"title":267},{"VI":268},"Kamilla Koch",{"id":270,"sortIndex":121,"researcher":24,"roles":271,"affiliations":272,"properties":281},"1e2ad045-d894-434a-9f8d-b2962335b6be",[147],[273],{"id":24,"sortIndex":102,"affiliation":274,"properties":24},{"id":275,"createTime":276,"updateTime":276,"relativeEntities":277,"slug":24,"properties":278,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"92974975-eaf7-4898-8f37-0cae527dceaa","2023-12-19T23:54:05.669+00:00",[],{"title":279},{"VI":280},"Ecology and Environmental Sciences, Halmstad University, Halmstad, Sweden",{"title":282},{"VI":283},"Göran Sahlén",{"id":285,"sortIndex":162,"researcher":24,"roles":286,"affiliations":287,"properties":296},"03ea025d-e0c2-4470-91d0-0b6f4ce5d2f0",[147],[288],{"id":24,"sortIndex":102,"affiliation":289,"properties":24},{"id":290,"createTime":291,"updateTime":291,"relativeEntities":292,"slug":24,"properties":293,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"bb6dd482-e24b-42ee-a43a-2223409cf0c3","2023-12-12T14:27:00.186+00:00",[],{"title":294},{"VI":295},"Department of Biology, Ecology Building, Lund University, Lund, Sweden",{"title":297},{"VI":298},"Maria Karlsson",{"url":226,"publisher":300,"properties":330},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":301,"slug":10,"properties":302,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":308,"manageAffiliations":309,"indexDatabases":310,"url":100,"thumbnailPath":24,"statistic":325,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":303,"issn":304,"introduce":305,"eissn":306,"title":307},{"VOID":13},{"VOID":15},{"EN":17},{"VOID":19},{"EN":21},[],[],[311,318],{"id":62,"indexDatabase":312,"url":77,"indexYears":24,"academicFieldIds":317,"indexDatabaseRanking":24},{"id":64,"createTime":65,"updateTime":66,"relativeEntities":313,"label":314,"description":315,"key":73,"publicationTags":316,"standard":24},[],{"EN":69,"VI":69},{"VI":71,"EN":72},[75,76],[79,80],{"id":82,"indexDatabase":319,"url":95,"indexYears":96,"academicFieldIds":324,"indexDatabaseRanking":99},{"id":84,"createTime":85,"updateTime":86,"relativeEntities":320,"label":321,"description":322,"key":92,"publicationTags":323,"standard":24},[],{"EN":89,"VI":89},{"EN":89,"VI":91},[94],[98],{"impactFactor":102,"impactFactorByYear":326,"i10Index":102,"i10IndexLast5Year":102,"totalPublication":104,"totalPublicationByYear":327,"totalCitation":102,"totalCitationByYear":328,"totalCitationPerPublication":102,"totalCitationPerPublicationByYear":329,"hindexLast5Year":102,"hindex":102},{},{"2001":58,"2002":106,"2003":58,"2004":106,"2005":107,"2006":58,"2007":108,"2008":109,"2009":110,"2010":111,"2011":111,"2012":112,"2013":113,"2014":114,"2015":115,"2016":116,"2017":117,"2018":114,"2019":113,"2020":118,"2021":119,"2022":120,"2023":58,"2024":121},{},{},{"volume":331,"pages":333},{"VOID":332},"12",{"VOID":334},"313-323","2012-06-22",2012,{"id":338,"createTime":339,"updateTime":340,"relativeEntities":341,"slug":342,"properties":343,"entityType":139,"verifyStatus":140,"verifyTime":340,"verifyNote":141,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102,"primaryUrl":352,"fullTextUrl":24,"authors":353,"publicationType":173,"publisherRelationship":382,"citationCount":24,"citationInfo":24,"publishDate":418,"publishYear":419,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":24,"isForceReanalyzing":212},"c89a3b6e-a760-43d7-8c82-c157a5a26541","2023-11-26T17:34:43.156+00:00","2024-12-20T23:52:17.848+00:00",[],"Sex-or-no-sex-Group-I-introns-and-independent-marker-genes-reveal-the-existence-of-three-sexual-but-reproductively-isolated-biospecies-in-Trichia-varia-Myxomycetes-",{"references":344,"abstract":346,"title":348,"doi":350},{"VOID":345},"Adl, 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Predicting the secondary structures and tertiary interactions of 211 group I introns in IE subgroup. Nucleic Acids Research, 33, 2118–2128.\nLieb, B. (2014). PCR Additives. http:\u002F\u002Fwww.staff.uni-mainz.de\u002Flieb\u002Fadditiva.html. Accessed 6 March 2014.\nLinne, C. (1792). Systema Naturae. Tom. II. Pars II. listed under the name Stemonitis. 1467–1470.\nLundblad, E. W., Einvik, C., Rønning, S., Haugli, K., & Johansen, S. (2004). Twelve group I introns in the same pre-rRNA transcript of the myxomycete Fuligo septica: RNA processing and evolution. Molecular Biology and Evolution, 21, 1283–1293.\nMachouart, M., Lacroix, C., Bui, H., Feuilhade de Chauvin, M., Derouin, F., & Lorenzo, F. (2004). Polymorphisms and intronic structures in the 18S subunit ribosomal RNA gene of the fungi Scytalidium dimidiatum and Scytalidium hyalinum. Evidence of an IC1 intron with an His-Cys endonuclease gene. FEMS Microbiology Letters, 238, 455–467.\nMarchler-Bauer, A., Zheng, C., Chitsaz, F., Derbyshire, M. K., Geer, L. Y., Geer, R. C., et al. (2013). CDD: conserved domains and protein three-dimensional structure. Nucleic Acids Research, 41, D348–D352.\nMartin, G. W., & Alexopoulos, C. J. (1969). The Myxomycetes. Iowa City: Iowa Univ. Press.\nMichel, F., & Westhof, E. (1990). Modelling of the three-dimensional architecture of group I catalytic introns based on comparative sequence analysis. Journal of Molecular Biology, 216, 585–610.\nMilne, I., Lindner, D., Bayer, M., Husmeier, D., McGuire, G., Marshall, D. F., & Wright, F. (2009). TOPALi v2: a rich graphical interface for evolutionary analyses of multiple alignments on HPC clusters and multi-core desktops. Bioinformatics, 25, 126–127.\nMilstein, D., Oliveira, M. C., Martins, F. M., & Matioli, S. R. (2008). Group I introns and associated homing endonuclease genes reveals a clinal structure for Porphyra spiralis var. amplifolia (Bangiales, Rhodophyta) along the eastern coast of South America. BMC Evolutionary Biology, 8, 308.\nMoriyama, Y., & Kawano, S. (2010). Maternal inheritance of mitochondria: multipolarity, multiallelism and hierarchical transmission of mitochondrial DNA in the true slime mold Physarum polycephalum. Journal of Plant Research, 123, 139–148.\nMüller, K. M., Cannone, J. J., Gutell, R. R., & Sheath, R. G. (2001). A structural and phylogenetic analysis of the group IC1 introns in the order Bangiales (Rhodophyta). Molecular Biology and Evolution, 18, 1654–1667.\nMuscarella, D. E., & Vogt, V. M. (1989). A mobile group I intron in the nuclear rDNA of Physarum polycephalum. Cell, 56, 443–454.\nMuscarella, D. E., & Vogt, V. M. (1993). A mobile group I intron from Physarum polycephalum can insert itself and induce point mutations in the nuclear ribosomal DNA of Saccharomyces cerevisiae. Molecular and Cellular Biology, 13, 1023–1033.\nMuscarella, D. E., Ellison, E. L., Ruoff, B. M., & Vogt, V. M. (1990). Characterization of I-Ppo, an intron-encoded endonuclease that mediates homing of a group I intron in the ribosomal DNA of Physarum polycephalum. Molecular and Cellular Biology, 10, 3386–3396.\nNandipati, S. C., Haugli, K., Coucheron, D. H., Haskins, E. F., & Johansen, S. D. (2012). Polyphyletic origin of the genus Physarum (Physarales, Myxomycetes) revealed by nuclear rDNA mini-chromosome analysis and group I intron synapomorphy. BMC Evolutionary Biology, 12, 166.\nNannenga-Bremekamp, N. B. (1991). A guide to temperate Myxomycetes (Feest A, Burgraff E: De Nederlandse Myxomyceten, Engl. transl.). Bristol: Biopress Lim.\nNeubert, H., Nowotny, W., & Baumann, K. (1993). Die Myxomyceten Deutschlands und des angrenzenden Alpenraumes unter besonderer Berücksichtigung Österreichs. Band 1. Ceratiomyxales, Echinosteliales, Liceales, Trichiales. Gomaringen: Baumann Verl.\nNielsen, H., & Johansen, S. D. (2009). Group I introns: moving in new directions. RNA Biology, 6, 375–383.\nNikoh, N., & Fukatsu, T. (2001). Evolutionary dynamics of multiple group I introns in nuclear ribosomal RNA genes of endoparasitic fungi of the genus Cordyceps. Molecular Biology and Evolution, 18, 1631–1642.\nNovozhilov, Y. K., Okun, M. V., Erastova, D. A., Shchepin, O. N., Zemlyanskaya, I. V., García-Carvajal, E., & Schnittler, M. (2013a). Description, culture and phylogenetic position of a new xerotolerant species of Physarum. Mycologia, 105, 1535–1546.\nNovozhilov, Y. K., Schnittler, M., Erastova, D. A., Okun, M. V., Schepin, O. N., & Heinrich, E. (2013b). Diversity of nivicolous myxomycetes of the Teberda State Biosphere Reserve (Northwestern Caucasus, Russia). Fungal Diversity, 59, 109–130.\nPawlowski, J., Audic, S., Adl, S., Bass, D., Belbahri, L., Berney, C., et al. (2012). CBOL protist working group: barcoding eukaryotic richness beyond the Animal, Plant, and Fungal kingdoms. PLoS Biology, 10, e1001419.\nPersoon, C. H. (1794). Neuer Versuch einer systematischen Eintheilung der Schwämme. Neues Magazin für die Botanik in ihrem ganzen Umfange, 1, 63–128.\nPoulain, M., Meyer, M., & Bozonnet, J. (2011). Les myxomycetes. Delémont: Féd. Mycol. Bot. Dauphiné-Savoie.\nRätzel, V., Ebeling, B., Hoffman, X. K., Tesmer, J., & Marwan, W. (2013). Physarum polycephalum mutants in the photocontrol of sporulation display altered patterns in the correlated expression of developmentally regulated genes. Development Growth and Differentiation, 55, 247–259.\nRonquist, F., & Huelsenbeck, J. P. (2003). MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics, 19, 1572–1574.\nRonquist, F., Teslenko, M., van der Mark, P., Ayres, D. L., Darling, A., Höhna, S., et al. (2012). MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology, 61, 539–542.\nSauer, H. W. (1982). Developmental Biology of Physarum. Cambridge: Cambridge University Press.\nSchnittler, M., & Mitchell, D. W. (2000). Species diversity in Myxomycetes based on the morphological species concept—a critical examination. Stapfia, 73, 55–62.\nSchnittler, M., & Tesmer, J. (2008). A habitat colonisation model for spore-dispersed organisms—does it work with eumycetozoans? Mycological Research, 112, 697–707.\nSchnittler, M., Novozhilov, Y. K., Romeralo, M., Brown, M., & Spiegel, F. W. (2012). Myxomycetes and Myxomycete-like organisms. In F. W. Stuttgart (Ed.), Englers Syllabus of Plant Families. Volume 4. 13th edition (pp. 40–88). Bornträger.\nSmirnov, A. V., Chao, E., Nassonova, E. S., & Cavalier-Smith, T. (2011). A revised classification of naked lobose amoebae (Amoebozoa: Lobosa). Protist, 162, 545–570.\nSTAR. (2014). StarORF. Software Tools for Academics and Researchers. http:\u002F\u002Fstar.mit.edu\u002Forf. Accessed 25 March 2014.\nStephenson, S. L., Schnittler, M., & Novozhilov, Y. K. (2008). Myxomycete diversity and distribution from the fossil record to the present. Biodiversity and Conservation, 17, 285–301.\nTamura, K., Nei, M., & Kumar, S. (2004). Prospects for inferring very large phylogenies by using the neighbor-joining method. Proceedings of the National Academy of Sciences of the United States of America, 101, 11030–11035.\nTamura, K., Peterson, D., Peterson, N., Stecher, G., Nei, M., & Kumar, S. (2011). MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Molecular Biology and Evolution, 28, 2731–2739.\nTanabe, Y., Yokota, A., & Sugiyama, J. (2002). Group I introns from Zygomycota: evolutionary implications for the fungal IC1 intron subgroup. Journal of Molecular Biology, 54, 692–702.\nTorres-Machorro, A. L., Hernández, R., Cevallos, A. M., & López-Villaseñor, I. (2010). Ribosomal RNA genes in eukaryotic microorganisms: witnesses of phylogeny? FEMS Microbiology Reviews, 34, 59–86.\nTraphagen, S. J., Dimarco, M. J., & Silliker, M. E. (2010). RNA editing of 10 Didymium iridis mitochondrial genes and comparison with the homologous genes in Physarum polycephalum. RNA, 16, 828–838.\nUrich, T., Lanzén, A., Qi, J., Huson, D. H., Schleper, C., & Schuster, S. C. (2008). Simultaneous assessment of soil microbial community structure and function through analysis of the meta-transcriptome. PLoS ONE, 3, e2527.\nVader, A., Nielsen, H., & Johansen, S. (1999). In vivo expression of the nucleolar group I intron-encoded I-DirI homing endonuclease involves the removal of a spliceosomal intron. The EMBO Journal, 18, 1003–1013.\nWalker, L. M., Dewsbury, D. R., Parks, S. S., Winsett, K. E., & Stephenson, S. L. (2011). The potential use of mitochondrial cytochrome c oxidase I for barcoding myxomycetes. In VII International Congress on Systematics and Ecology of Myxomycetes: 11–16 September 2011; Recife, Brazil (pp. 138).\nWikmark, O. G., Haugen, P., Haugli, K., & Johansen, S. D. (2007a). Obligatory group I introns with unusual features at positions 1949 and 2449 in nuclear LSU rDNA of Didymiaceae myxomycetes. Molecular Phylogenetics and Evolution, 43, 596–604.\nWikmark, O. G., Haugen, P., Lundblad, E. W., Haugli, K., & Johansen, S. D. (2007b). The molecular evolution and structural organization of group I introns at position 1389 in nuclear small subunit rDNA of myxomycetes. Journal of Eukaryotic Microbiology, 54, 49–56.\nXu, C., Wang, C., Sun, X., Zhang, R., Gleason, M. L., Eiji, T., & Sun, G. (2013). Multiple group I introns in the small-subunit rDNA of Botryosphaeria dothidea: implication for intraspecific genetic diversity. PLoS ONE, 8, e67808.\nYokoyama, E., Yamagishi, K., & Hara, A. (2002). Group-I intron containing a putative homing endonuclease gene in the small subunit ribosomal DNA of Beauveria bassiana IFO 31676. Molecular Biology and Evolution, 19, 2022–2025.\nZhou, Y., Lu, C., Wu, Q. J., Wang, Y., Sun, Z. T., Deng, J. C., & Zhang, Y. (2008). GISSD: group I intron sequence and structure database. Nucleic Acids Research, 36, D31–D37.",{"EN":347},"Plasmodial slime molds are members of the class Amoebozoa forming elaborate fruit bodies releasing airborne spores. Two species concepts have been developed independently: a morphological relying on fruit body characters, and a biological relying on crossing studies of a few cultivable species. In an attempt to reconcile both concepts, we obtained for 198 specimens of the common species Trichia varia partial sequences of three independent markers (nuclear small-subunit (SSU) ribosomal RNA gene, extrachromosomal; elongation factor 1 alpha gene, chromosomal; cytochrome oxidase subunit 1 gene, mitochondrial). The resulting phylogeny revealed 21 three-marker genotypes clustering into three groups. Combinations of the single-marker genotypes occurred exclusively within these groups, called 1, 2a, and 2b. To examine the suitability of group I introns to monitor speciation events, complete SSU sequences were generated for 66 specimens, which revealed six positions that can carry group I introns. For each of the groups 1 and 2a, five of these positions were occupied by different intron genotypes; and no genotype was shared by the two groups. Group 2b was devoid of introns. Putatively functional or degenerated homing endonuclease genes were found at different positions in groups 1 and 2a. All observations (genotypic combinations of the three markers, signs of recombination, intron patterns) fit well into a pattern of three cryptic biological species that reproduce predominantly sexual but are reproductively isolated. The pattern of group I introns and inserted homing endonuclease genes mounts evidence that the Goddard-Burt intron life cycle model applies to naturally occurring myxomycete populations.",{"EN":349},"Sex or no sex? 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of the Ibero-Maghrebian red-eyed grass snake (Natrix astreptophora)",{"VOID":436},"10.1007\u002Fs13127-017-0354-2",[438],"EN","http:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs13127-017-0354-2",[441,462,488,508,535,549],{"id":442,"sortIndex":443,"researcher":24,"roles":444,"affiliations":445,"properties":455},"bcda9c89-5cb5-43a0-b3f1-814959691ee4",4,[],[446],{"id":24,"sortIndex":102,"affiliation":447,"properties":24},{"id":448,"createTime":449,"updateTime":449,"relativeEntities":450,"slug":451,"properties":452,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"2003a780-c3a6-4efa-acb5-33f42a97b44f","2024-04-14T23:00:19.956+00:00",[],"Centre-d-Ecologie-Fonctionnelle-et-Evolutive-UMR-5175-Ecole-Pratique-des-Hautes-Etudes-PSL-Research-University-Montpellier-Cedex-5-France",{"title":453},{"EN":454},"Centre d’Ecologie Fonctionnelle et Evolutive – UMR 5175, Ecole Pratique des Hautes Etudes, PSL 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Spain",{"id":24,"sortIndex":102,"affiliation":475,"properties":24},{"id":476,"createTime":477,"updateTime":477,"relativeEntities":478,"slug":479,"properties":480,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"d8eeb745-1449-45dc-81e8-21fb8ece759c","2024-04-14T23:00:19.902+00:00",[],"Departament-de-Ci%C3%A8ncia-Animal-Universitat-de-Lleida-Lleida-Spain",{"title":481},{"EN":482},"Departament de Ciència Animal, Universitat de Lleida, Lleida, Spain",{"openalex":484,"title":486},{"VOID":485},"A5038188713",{"EN":487},"Philip de Pous",{"id":489,"sortIndex":490,"researcher":24,"roles":491,"affiliations":492,"properties":501},"4ae0df1c-262c-4af8-8d40-75cf59b72037",5,[],[493],{"id":24,"sortIndex":102,"affiliation":494,"properties":24},{"id":495,"createTime":496,"updateTime":496,"relativeEntities":497,"slug":24,"properties":498,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"3e2718d6-40ca-4227-8488-929a5e839987","2023-12-27T15:54:57.211+00:00",[],{"title":499},{"VI":500},"Museum of Zoology (Museum für Tierkunde), Dresden, Germany",{"openalex":502,"orcid":504,"title":506},{"VOID":503},"A5083864467",{"VOID":505},"https:\u002F\u002Forcid.org\u002F0000-0002-6740-7214",{"EN":507},"Uwe Fritz",{"id":509,"sortIndex":25,"researcher":24,"roles":510,"affiliations":511,"properties":530},"4a2e2b1d-954c-4526-80e5-6b6b9c577e13",[],[512,521],{"id":24,"sortIndex":102,"affiliation":513,"properties":24},{"id":514,"createTime":515,"updateTime":515,"relativeEntities":516,"slug":517,"properties":518,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"39e6833f-529a-4e36-aeb3-3725dbba26f1","2024-04-18T01:44:28.431+00:00",[],"Centre-d-Ecologie-Fonctionnelle-et-Evolutive-UMR-5175-CNRS-Montpellier-Cedex-5-France",{"title":519},{"EN":520},"Centre d’Ecologie Fonctionnelle et Evolutive UMR 5175, CNRS, Montpellier Cedex 5, France",{"id":24,"sortIndex":102,"affiliation":522,"properties":24},{"id":523,"createTime":524,"updateTime":524,"relativeEntities":525,"slug":526,"properties":527,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"bede9216-1754-4b0b-903d-17eddffededa","2024-04-14T23:00:19.943+00:00",[],"Naturalia-Environnement-Baillargues-France",{"title":528},{"EN":529},"Naturalia Environnement, Baillargues, France",{"openalex":531,"title":533},{"VOID":532},"A5063937619",{"EN":534},"Menad 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Vogel (Eds.), Evolving genes and proteins (pp. 97–166). New York: Academic Press.",{"EN":920},"Scorpions (Arachnida: Scorpiones Koch, 1837) are an ancient chelicerate arthropod lineage characterised by distinctive subdivision of the opisthosoma and venomous toxicity. The crown group is represented by over 2400 extant species, and unambiguous fossil representatives are known at least from the Cretaceous Period. However, a number of extinct scorpion lineages existed in the Palaeozoic Era, many of which are of a contentious marine (or at least semi-aquatic) lifestyle, and have long caused confusion regarding the nature of arachnid terrestrialization and arachnid phylogeny more broadly. To clarify the process of terrestrialization, there is a need to marry fossil and extant scorpions in a common evolutionary framework utilising modern advances in phylogenetics. Here, we review phylogenetic hypotheses of arachnid and scorpion interrelationships, relevant advances in phylogenetic divergence time estimation and the scorpion fossil record—especially with reference to terrestrialization. In addition, we provide a list of scorpion fossil calibrations for use in molecular dating and demonstrate their utility in deriving a novel scorpion time tree using Bayesian relaxed-clock methods. Our results reveal a window of divergence from 335 to 266 Mya for the scorpion crown group, consistent with a Pangean origin of crown scorpions inferred from the biogeographical distribution of the extant fauna.",{"EN":922},"Exploring the evolution and terrestrialization of scorpions (Arachnida: Scorpiones) with rocks and clocks",{"VOID":924},"10.1007\u002Fs13127-019-00390-7","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs13127-019-00390-7",[927,942,957,986,1008],{"id":928,"sortIndex":162,"researcher":24,"roles":929,"affiliations":930,"properties":939},"b9fe617f-ba23-4b93-9dd8-6229cb07a428",[147],[931],{"id":24,"sortIndex":102,"affiliation":932,"properties":24},{"id":933,"createTime":934,"updateTime":934,"relativeEntities":935,"slug":24,"properties":936,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"87e6f917-cbf0-4a07-8c93-04d1956491f4","2023-12-31T16:03:37.097+00:00",[],{"title":937},{"VI":938},"Department of Earth Sciences, The Natural History Museum, London, UK",{"title":940},{"VI":941},"Gregory D. Edgecombe",{"id":943,"sortIndex":25,"researcher":24,"roles":944,"affiliations":945,"properties":954},"e3435d7f-31da-426a-89d5-4fc94246153e",[147],[946],{"id":24,"sortIndex":102,"affiliation":947,"properties":24},{"id":948,"createTime":949,"updateTime":949,"relativeEntities":950,"slug":24,"properties":951,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"853dfaa7-ea73-4790-b767-57b501163f4d","2024-01-03T13:10:42.686+00:00",[],{"title":952},{"VI":953},"School of Earth Sciences and School of Biological Sciences, University of Bristol, Bristol, UK",{"title":955},{"VI":956},"Davide Pisani",{"id":958,"sortIndex":102,"researcher":24,"roles":959,"affiliations":960,"properties":983},"a1a523a3-3746-4487-bec3-83bccb88f870",[147],[961,968,975],{"id":962,"sortIndex":121,"affiliation":963,"properties":967},"d8d321ef-44ab-454e-b15b-2392b148067f",{"id":948,"createTime":949,"updateTime":949,"relativeEntities":964,"slug":24,"properties":965,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},[],{"title":966},{"VI":953},{},{"id":969,"sortIndex":162,"affiliation":970,"properties":974},"a7623488-c73d-4a99-98c0-fbbe40bd63e3",{"id":933,"createTime":934,"updateTime":934,"relativeEntities":971,"slug":24,"properties":972,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},[],{"title":973},{"VI":938},{},{"id":24,"sortIndex":102,"affiliation":976,"properties":24},{"id":977,"createTime":978,"updateTime":978,"relativeEntities":979,"slug":24,"properties":980,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"8dc72d41-8973-47b0-a22d-801c5c0a59e0","2024-01-03T13:10:42.643+00:00",[],{"title":981},{"VI":982},"Department of Biosciences, University of Exeter, Cornwall, UK",{"title":984},{"VI":985},"Richard J. Howard",{"id":987,"sortIndex":443,"researcher":24,"roles":988,"affiliations":989,"properties":1005},"6ef26b97-4d6f-4bde-a8a8-248e8de45f90",[147],[990,997],{"id":991,"sortIndex":162,"affiliation":992,"properties":996},"f1b51bfa-bc97-4cdf-80ac-76a48c5be9d7",{"id":948,"createTime":949,"updateTime":949,"relativeEntities":993,"slug":24,"properties":994,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},[],{"title":995},{"VI":953},{},{"id":24,"sortIndex":102,"affiliation":998,"properties":24},{"id":999,"createTime":1000,"updateTime":1000,"relativeEntities":1001,"slug":24,"properties":1002,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"34eb8261-e026-4ac5-ab9b-6c45561315c7","2023-12-27T03:49:43.990+00:00",[],{"title":1003},{"VI":1004},"Department of Evolutionary Biology, Ecology, and Environmental Sciences and Biodiversity Research Institute (IrBIO), University of Barcelona, Barcelona, Spain",{"title":1006},{"VI":1007},"Jesus Lozano-Fernandez",{"id":1009,"sortIndex":121,"researcher":24,"roles":1010,"affiliations":1011,"properties":1022},"e765ffe8-2709-4105-923e-9d9081a36674",[147],[1012],{"id":24,"sortIndex":102,"affiliation":1013,"properties":24},{"id":1014,"createTime":1015,"updateTime":1016,"relativeEntities":1017,"slug":1018,"properties":1019,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"1fa93d17-6ad1-4bd1-9c3d-22062bf819c4","2023-12-31T07:37:59.604+00:00","2024-10-10T17:33:28.731+00:00",[],"School-of-Earth-and-Environmental-Sciences-University-of-Manchester-Manchester-UK",{"title":1020},{"VI":1021},"School of Earth and Environmental Sciences, University of Manchester, Manchester, UK",{"title":1023},{"VI":1024},"David A. Legg",{"url":925,"publisher":1026,"properties":1056},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":1027,"slug":10,"properties":1028,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":1034,"manageAffiliations":1035,"indexDatabases":1036,"url":100,"thumbnailPath":24,"statistic":1051,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":1029,"issn":1030,"introduce":1031,"eissn":1032,"title":1033},{"VOID":13},{"VOID":15},{"EN":17},{"VOID":19},{"EN":21},[],[],[1037,1044],{"id":62,"indexDatabase":1038,"url":77,"indexYears":24,"academicFieldIds":1043,"indexDatabaseRanking":24},{"id":64,"createTime":65,"updateTime":66,"relativeEntities":1039,"label":1040,"description":1041,"key":73,"publicationTags":1042,"standard":24},[],{"EN":69,"VI":69},{"VI":71,"EN":72},[75,76],[79,80],{"id":82,"indexDatabase":1045,"url":95,"indexYears":96,"academicFieldIds":1050,"indexDatabaseRanking":99},{"id":84,"createTime":85,"updateTime":86,"relativeEntities":1046,"label":1047,"description":1048,"key":92,"publicationTags":1049,"standard":24},[],{"EN":89,"VI":89},{"EN":89,"VI":91},[94],[98],{"impactFactor":102,"impactFactorByYear":1052,"i10Index":102,"i10IndexLast5Year":102,"totalPublication":104,"totalPublicationByYear":1053,"totalCitation":102,"totalCitationByYear":1054,"totalCitationPerPublication":102,"totalCitationPerPublicationByYear":1055,"hindexLast5Year":102,"hindex":102},{},{"2001":58,"2002":106,"2003":58,"2004":106,"2005":107,"2006":58,"2007":108,"2008":109,"2009":110,"2010":111,"2011":111,"2012":112,"2013":113,"2014":114,"2015":115,"2016":116,"2017":117,"2018":114,"2019":113,"2020":118,"2021":119,"2022":120,"2023":58,"2024":121},{},{},{"volume":1057,"pages":1059},{"VOID":1058},"19",{"VOID":1060},"71-86","2019-02-06",2019,{"id":1064,"createTime":1065,"updateTime":1066,"relativeEntities":1067,"slug":1068,"properties":1069,"entityType":139,"verifyStatus":140,"verifyTime":1066,"verifyNote":141,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102,"primaryUrl":1078,"fullTextUrl":24,"authors":1079,"publicationType":173,"publisherRelationship":1136,"citationCount":24,"citationInfo":24,"publishDate":1170,"publishYear":1171,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":24,"isForceReanalyzing":212},"34c17a80-edbd-4e7f-90c0-db93e1c7285f","2023-11-24T19:08:57.550+00:00","2024-12-27T23:39:38.790+00:00",[],"Exploring-the-diversity-of-the-Malagasy-Ponera-Hymenoptera-Formicidae-fauna-via-integrative-taxonomy",{"references":1070,"abstract":1072,"title":1074,"doi":1076},{"VOID":1071},"Ali, J. 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PLoS ONE, 3(5), e1787. https:\u002F\u002Fdoi.org\u002F10.1371\u002Fjournal.pone.0001787\nGodfrey, L. R., Samonds, K. E., Baldwin, J. W., Sutherland, M. R., Kamilar, J. M., & Allfisher, K. L. (2020). Mid-Cenozoic climate change, extinction, and faunal turnover in Madagascar, and their bearing on the evolution of lemurs. BMC Evolutionary Biology, 20(1), 1–18. https:\u002F\u002Fdoi.org\u002F10.1186\u002Fs12862-020-01628-1\nGoodman, S. M., & Benstead, J. P. (2005). Updated estimates of biotic diversity and endemism for Madagascar. Oryx, 39, 73–77. https:\u002F\u002Fdoi.org\u002F10.1017\u002FS0030605305000128\nHita-Garcia, F., & Fisher, B. L. (2014). The hyper-diverse ant genus Tetramorium Mayr (Hymenoptera, Formicidae) in the Malagasy region taxonomic revision of the T. naganum, T. plesiarum, T. schaufussii, and T. severini species groups. ZooKeys, 413, 1–170. https:\u002F\u002Fdoi.org\u002F10.3897\u002Fzookeys.413.7172\nhttps:\u002F\u002Fwww.antcat.org\u002F. Retrieved from November 19, 2022.\nLanfear, R., Frandsen, P. B., Wright, A. M., Senfeld, T., & Calcott, B. (2016). PartitionFinder 2: New methods for selecting partitioned models of evolution formolecular and morphological phylogenetic analyses. Molecular Biology and Evolution, 34(3), 772–773. https:\u002F\u002Fdoi.org\u002F10.1093\u002Fmolbev\u002Fmsw260\nLeong, C.-M., Guénard, B., Shiao, S.-F., & Lin, C.-C. (2019). Taxonomic revision of the genus Ponera Latreille, 1804 (Hymenoptera: Formicidae) of Taiwan and Japan, with a key to East Asian species. Zootaxa, 4594, 1–86. https:\u002F\u002Fdoi.org\u002F10.11646\u002Fzootaxa.4594.1.1\nMasters, J. C., Génin, F., Zhang, Y., Pellen, R., Huck, T., Mazza, P. P., ... & Aslanian, D. (2020). Biogeographic mechanisms involved in the colonization of Madagascar by African vertebrates: Rifting, rafting and runways. Journal of Biogeography, 48(3), 492–510. https:\u002F\u002Fdoi.org\u002F10.1111\u002Fjbi.14032\nPadial, J. M., Miralles, A., De la Riva, I., & Vences, M. (2010). The integrative future of taxonomy. Frontiers in Zoology, 7(1), 1–14. https:\u002F\u002Fdoi.org\u002F10.1186\u002F1742-9994-7-16\nPerrault, G. H. (1993). Peuplement en fourmis de l’atoll de Fangataufa. Bulletin De La Société Entomologique De France, 98, 323–338.\nR Core Team. (2020). A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL https:\u002F\u002Fwww.R-project.org\u002F. R version 4.0.2 (2020–06–22).\nRakotonirina, J. C., Csősz, S., & Fisher, B. L. (2016). Revision of the Malagasy Camponotus edmondi species group (Hymenoptera, Formicidae, Formicinae): Integrating qualitative morphology and multivariate morphometric analysis. ZooKeys, 572, 81–154. https:\u002F\u002Fdoi.org\u002F10.3897\u002Fzookeys.572.7177\nRasoamanana, N., Csősz, S., & Fisher, B. L. (2017). Taxonomic revision of imitating carpenter ants, Camponotus subgenus Myrmopytia (Hymenoptera, Formicidae) of Madagascar, using morphometry and qualitative traits. ZooKeys, 681, 119–152. https:\u002F\u002Fdoi.org\u002F10.3897\u002Fzookeys.681.13187\nSalata, S., & Fisher, B. L. (2021). Taxonomic revision of Madagascan species of the Pheidole fervens species-group (Hymenoptera, Formicidae). PLoS ONE, 16(1), e0244195. https:\u002F\u002Fdoi.org\u002F10.1371\u002Fjournal.pone.0244195\nSamonds, K. E., Godfrey, L. R., Ali, J. R., Goodman, S. M., Vences, M., Sutherland, M. R., Irwin, M. T., Krause, D. W. (2013). Imperfect isolation: Factors and filters shaping Madagascar’s extant vertebrate fauna. PLoS ONE, 8(4), e62086. https:\u002F\u002Fdoi.org\u002F10.1371\u002Fjournal.pone.0062086\nSchlick-Steiner, B. C., Steiner, F. M., Seifert, B., Stauffer, C., Christian, E., & Crozier, R. H. (2010). Integrative taxonomy: A multisource approach to exploring biodiversity. Annual Review of Entomology, 55, 421–438.\nSeifert, B. (2020). The Gene and Gene Expression (GAGE) species concept–An universal approach for all eukaryotic organisms. Systematic Biology, 69, 1033–1038.\nSeifert, B., Ritz, M., & Csősz, S. (2014). Application of exploratory data analyses opens a new perspective in morphology-based alpha-taxonomy of eusocial organisms. Myrmecological News, 19, 1–15.\nSukumaran, J., & Holder, M. T. (2010). DendroPy: A Python library for phylogenetic computing. Bioinformatics, 26, 1569–1571. https:\u002F\u002Fdoi.org\u002F10.1093\u002Fbioinformatics\u002Fbtq228\nSukumaran, J. & Holder, M. T. (2015). SumTrees: Phylogenetic Tree Summarization. 4.0.0 (Jan 31 2015). Available at https:\u002F\u002Fgithub.com\u002Fjeetsukumaran\u002FDendroPy\nTaylor, R. W. (1967). A monographic revision of the ant genus Ponera Latreille (Hymenoptera: Formicidae). Pacific Insects Monograph, 13, 1–112.\nWheeler, W. M. (1933). Three obscure genera of ponerine ants. American Museum Novitates, 672, 1–23.\nWilson, E. O. (1957). The tenuis and selenophora groups of the ant genus Ponera (Hymenoptera: Formicidae). Bulletin of the Museum of Comparative Zoology, 116(6), 355–386.",{"EN":1073},"The genus Ponera includes over 60 extant species worldwide. These tiny, endogeic predator ants are predominantly distributed in the Indomalaya and Australasia regions, with a few additional Holarctic species. Herein, we explore and describe the diversity of the Malagasy Ponera fauna through an integrative taxonomic approach. We obtained our morphological species hypotheses from multivariate analyses of ten continuous morphometric characters. Species boundaries and reliability of morphological clusters were tested via confirmatory Linear Discriminant Analysis (LDA), cross-validation (LOOCV), and analyses of a mitochondrial COI gene fragment. According to the combined application of the analyses, altogether, three species are inferred in the Malagasy region, Ponera petila Wilson (1957), P. swezeyi Wheeler (1933), and P. adumbrans Csősz & Fisher sp. n. Ponera petila and P. swezeyi belong to the Indo-Australian Ponera tenuis group; the third species, P. adumbrans sp. n., is morphologically similar to the Papua New Guinean P. clavicornis Emery (1900). Furthermore, Linear Discriminant Analysis classified the type specimens of P. bableti Perrault (1993), along with a P. petila cluster with posterior p = 1. Therefore, we propose the new junior synonymy of P. bableti with P. petila. Madagascar’s extant biodiversity is predominantly explained by colonization events from the African continent across the Mozambique channel via rafting. However, since no native Ponera species are known from the Afrotropical continent, and the closest congeners have an almost exclusively Indo-Australian distribution, the likelihood of an Indo-Australian origin of the Malagasy Ponera fauna is implied.\n",{"EN":1075},"Exploring the diversity of the Malagasy Ponera (Hymenoptera: Formicidae) fauna via integrative taxonomy",{"VOID":1077},"10.1007\u002Fs13127-023-00610-1","https:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs13127-023-00610-1",[1080,1095,1121],{"id":1081,"sortIndex":162,"researcher":24,"roles":1082,"affiliations":1083,"properties":1092},"026dc229-8ef6-4383-abeb-7638cafd9319",[147],[1084],{"id":24,"sortIndex":102,"affiliation":1085,"properties":24},{"id":1086,"createTime":1087,"updateTime":1087,"relativeEntities":1088,"slug":24,"properties":1089,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"7dcc69f7-957d-4cf0-8e36-dd111ca0297c","2024-01-17T14:08:06.554+00:00",[],{"title":1090},{"VI":1091},"National Institute of the Atlantic Forest, Santa Teresa, Brazil",{"title":1093},{"VI":1094},"Ana C. Loss",{"id":1096,"sortIndex":102,"researcher":24,"roles":1097,"affiliations":1098,"properties":1118},"b5737dc0-466b-4c2b-885d-a853f2fa9958",[147],[1099,1107],{"id":24,"sortIndex":102,"affiliation":1100,"properties":24},{"id":1101,"createTime":1102,"updateTime":1102,"relativeEntities":1103,"slug":24,"properties":1104,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"4f0f8bdf-b793-4d19-aab4-2e38ebc2ff01","2023-12-19T20:38:05.361+00:00",[],{"title":1105},{"VI":1106},"ELKH-ELTE-MTM Integrative Ecology Research Group, Budapest, Hungary",{"id":1108,"sortIndex":162,"affiliation":1109,"properties":1117},"c822b3b6-2e5a-47f6-86df-a0de3fcbd71b",{"id":1110,"createTime":1111,"updateTime":1111,"relativeEntities":1112,"slug":1113,"properties":1114,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"abd21227-5adf-4a94-82ad-36f0bff438ef","2023-11-24T19:08:57.560+00:00",[],"Department-of-Systematic-Zoology-and-Ecology-Institute-of-Biology-ELTE-E%C3%B6tv%C3%B6s-Lor%C3%A1nd-University-Budapest-Hungary",{"title":1115},{"VI":1116},"Department of Systematic Zoology and Ecology, Institute of Biology, ELTE-Eötvös Loránd University, Budapest, Hungary",{},{"title":1119},{"VI":1120},"Sándor Csősz",{"id":1122,"sortIndex":121,"researcher":24,"roles":1123,"affiliations":1124,"properties":1133},"1943ea3b-eb56-49d8-b0af-4d02903f3843",[147],[1125],{"id":24,"sortIndex":102,"affiliation":1126,"properties":24},{"id":1127,"createTime":1128,"updateTime":1128,"relativeEntities":1129,"slug":24,"properties":1130,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"33cb0763-fd25-4fbb-a192-a43a76288a1a","2023-12-06T20:32:38.030+00:00",[],{"title":1131},{"VI":1132},"Entomology, California Academy of Sciences, San Francisco, USA",{"title":1134},{"VI":1135},"Brian L. Fisher",{"url":1078,"publisher":1137,"properties":1167},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":1138,"slug":10,"properties":1139,"entityType":22,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":25,"subjectFields":1145,"manageAffiliations":1146,"indexDatabases":1147,"url":100,"thumbnailPath":24,"statistic":1162,"gsStatistic":24,"type":24,"analyzePriority":24},[],{"country":1140,"issn":1141,"introduce":1142,"eissn":1143,"title":1144},{"VOID":13},{"VOID":15},{"EN":17},{"VOID":19},{"EN":21},[],[],[1148,1155],{"id":62,"indexDatabase":1149,"url":77,"indexYears":24,"academicFieldIds":1154,"indexDatabaseRanking":24},{"id":64,"createTime":65,"updateTime":66,"relativeEntities":1150,"label":1151,"description":1152,"key":73,"publicationTags":1153,"standard":24},[],{"EN":69,"VI":69},{"VI":71,"EN":72},[75,76],[79,80],{"id":82,"indexDatabase":1156,"url":95,"indexYears":96,"academicFieldIds":1161,"indexDatabaseRanking":99},{"id":84,"createTime":85,"updateTime":86,"relativeEntities":1157,"label":1158,"description":1159,"key":92,"publicationTags":1160,"standard":24},[],{"EN":89,"VI":89},{"EN":89,"VI":91},[94],[98],{"impactFactor":102,"impactFactorByYear":1163,"i10Index":102,"i10IndexLast5Year":102,"totalPublication":104,"totalPublicationByYear":1164,"totalCitation":102,"totalCitationByYear":1165,"totalCitationPerPublication":102,"totalCitationPerPublicationByYear":1166,"hindexLast5Year":102,"hindex":102},{},{"2001":58,"2002":106,"2003":58,"2004":106,"2005":107,"2006":58,"2007":108,"2008":109,"2009":110,"2010":111,"2011":111,"2012":112,"2013":113,"2014":114,"2015":115,"2016":116,"2017":117,"2018":114,"2019":113,"2020":118,"2021":119,"2022":120,"2023":58,"2024":121},{},{},{"pages":1168},{"VOID":1169},"1-11","2023-06-28",2023,{"id":1173,"createTime":1174,"updateTime":1175,"relativeEntities":1176,"slug":1177,"properties":1178,"entityType":139,"verifyStatus":140,"verifyTime":1175,"verifyNote":141,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102,"primaryUrl":1187,"fullTextUrl":24,"authors":1188,"publicationType":173,"publisherRelationship":1271,"citationCount":24,"citationInfo":24,"publishDate":1306,"publishYear":419,"citationAnalyzeStatus":23,"lastCitationAnalyze":24,"indexDatabases":24,"openAccess":24,"references":24,"isForceReanalyzing":212},"ead6a7cb-37c7-4e9a-b371-637aad7cf2b5","2023-12-02T17:59:12.339+00:00","2025-02-23T23:38:14.689+00:00",[],"Two-tribes-hidden-in-one-genus-the-case-of-Agaedioxenis-Villeneuve-Diptera-Tachinidae-Exoristinae-",{"references":1179,"abstract":1181,"title":1183,"doi":1185},{"VOID":1180},"Cerretti, P., & Barraclough, D. A. (2007). Anomalostomyia namibica, a new genus and species of Afrotropical Tachinidae (Diptera). Italian Journal of Zoology, 74, 101–106.\nCerretti, P., O’Hara, J. E., Stireman, J. O., III, Winkler, I. S., & Kirk-Spriggs, A. H. (2013). To ‘Die Hel’ and back. Expeditions of the phylogeny of World Tachinidae Project. Part I: Western Cape, South Africa. The Tachinid Times, 26, 20–29.\nCerretti, P., Di Giulio, A., Romani, R., Inclan, D. J., Whitmore, D., Di Giovanni, F., Scalici, M., & Minelli, A. (2014a). First report of exocrine epithelial glands in oestroid flies: the tachinid sexual patches (Diptera: Calyptratae: Oestroidea: Tachinidae). Acta Zoologica. doi:10.1111\u002Fazo.12085.\nCerretti, P., O’Hara, J. E., Wood, D. M., Shima, H., Inclan, D. J., & Stireman, J. O., III. (2014b). Signal through the noise? Phylogeny of the Tachinidae (Diptera) as inferred from morphological evidence. Systematic Entomology, 39, 335–353.\nCrosskey, R. W. (1973). A conspectus of the Tachinidae (Diptera) of Australia, including keys to the supraspecific taxa and taxonomic and host catalogues. Bulletin of the British Museum (Natural History). Entomology. Supplement, 21, 221 pp.\nCrosskey, R. W. (1976). A taxonomic conspectus of the Tachinidae (Diptera) of the Oriental Region. Bulletin of the British Museum (Natural History). Entomology. Supplement, 26, 357 pp.\nCrosskey, R. W. (1980). Family Tachinidae. In R. W. Crosskey (Ed.), Catalogue of the Diptera of the Afrotropical Region (pp. 822–882). London: British Museum (Natural History).\nCrosskey, R. W. (1984). Annotated keys to the genera of Tachinidae (Diptera) found in tropical and southern Africa. Annals of the Natal Museum, 26, 189–237.\nEvenhuis, N. L., Pape, T., & Pont, A. C. (2008). The problems of subsequent typification in genus-group names and use of the Zoological Record: a study of selected post-1930 Diptera genus-group names without type species designations. Zootaxa, 1912, 1–44.\nEvenhuis, N. L., Pont, A. C., & Whitmore, D. (2015). Nomenclatural studies toward a world list of Diptera genus-group names. Part IV: Charles Henry Tyler Townsend. Zootaxa.\nHerting, B. (1957). Das weibliche Postabdomen des calyptraten Fliegen (Diptera) und sein Merkmalswert für die Systematik der Gruppe. Zeitschrift für Morphologie und Ökologie der Tiere, 45, 429–461.\nHerting, B. (1960). Biologie der westpaläarktischen Raupenfliegen. Dipt., Tachinidae. Monographien zur angewandten Entomologie, 16, 188 pp.\nInternational Commission on Zoological Nomenclature. (1999). International Code of Zoological Nomenclature. Fourth edition adopted by the International Union of Biological Sciences. London: International Trust for Zoological Nomenclature.\nMcAlpine, J. F. (1981). Morphology and terminology — adults. In McAlpine, J. F. Peterson, B. V. Shewell, G. E. Teskey, H. J. Vockeroth, J. R. & Wood, D. M. (Eds), Manual of Nearctic Diptera. Vol. 1. Research Branch, Agriculture Canada Monograph, 27, 9–63.\nMellini, E. (1991). Sinossi di biologia dei Ditteri Larvevoridi. Bollettino dell’Istituto di Entomologia “Guido Grandi” dell’Università di Bologna, 45(1990), 1–38.\nMesnil, L. P. (1975). 64g. Larvaevorinae (Tachininae). Die Fliegender Palaearktischen Region, 10 (Lieferung 309), 1305–1384.\nO’Hara, J. E. (2002). Revision of the Polideini (Tachinidae) of America north of Mexico. Studia Dipterologica. Supplement, 10, 170 pp.\nO’Hara, J. E. (2013). History of tachinid classification (Diptera, Tachinidae). ZooKeys, 316, 1–34.\nO’Hara, J. E. (2014). World genera of the Tachinidae (Diptera) and their regional occurrence. Version 8.0. PDF document, 87 pp. http:\u002F\u002Fwww.nadsdiptera.org\u002FTach\u002FWorldTachs\u002FGenera [verified November 2014].\nRambaut, A. (2014). FigTree 1.4.1. Tree Figure Drawing Tool (http:\u002F\u002Ftree.bio.ed.ac.uk\u002F).\nRambaut, A., Suchard, M. A., Xie, D., & Drummond, A. J. (2014). Tracer v1.6, Available from http:\u002F\u002Fbeast.bio.ed.ac.uk\u002FTracer.\nRatnasingham, S., & Hebert, P. D. N. (2007). BOLD: The Barcode of Life Data System (http:\u002F\u002Fwww.barcodinglife.org). Molecular Ecology Notes, 7, 355–364.\nRokas, A., & Carroll, S. B. (2005). More genes or more taxa? The relative contribution of gene number and taxon number to phylogenetic accuracy. Molecular Biology and Evolution, 22, 1337–1344.\nRonquist, F., & Huelsenbeck, J. P. (2003). MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics, 19, 1572–1574.\nSmith, M. A., Woodley, N. E., Janzen, D. H., Hallwachs, W., & Hebert, P. D. N. (2006). DNA barcodes reveal cryptic host-specificity within the presumed polyphagous members of a genus of parasitoid flies (Diptera: Tachinidae). Proceedings of the National Academy of Sciences USA, 103, 3657–3662.\nSmith, M. A., Wood, D. M., Janzen, D. H., Hallwachs, W., & Hebert, P. D. N. (2007). DNA barcodes affirm that 16 species of apparently generalist tropical parasitoid flies (Diptera: Tachinidae) are not all generalists. Proceedings of the National Academy of Sciences USA, 104, 4967–4972.\nStamatakis, A. (2014). RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics. doi:10.1093\u002Fbioinformatics\u002Fbtu033.\nStireman, J. O., III. (2002). Phylogenetic relationships of tachinid flies in subfamily Exoristinae (Tachinidae: Diptera) based on 28S rDNA and elongation factor-1α. Systematic Entomology, 27, 409–435.\nStireman, J. O., III, O’Hara, J. E., Moulton, K., Cerretti, P., & Winkler, I. S. (2013). Progress towards a phylogeny of world Tachinidae. Year 1. The Tachinid Times, 26, 4–9.\nTachi, T., & Shima, H. (2010). Molecular phylogeny of the subfamily Exoristinae (Diptera, Tachinidae), with discussions on the evolutionary history of female oviposition strategy. Systematic Entomology, 35, 148–163.\nTamura, K., Stecher, G., Peterson, D., Filipski, A., & Kumar, S. (2013). MEGA6: molecular evolutionary genetics analysis version 6.0. Molecular Biology and Evolution, 30, 2725–2729.\nTownsend, C. H. T. (1943) Addenda and corrigenda [to Townsend’s Manual of myiology in twelve parts, Part XI, 1941]. Privately published, Itaquaquecetuba, São Paulo. Pp. 331–342.\nTschorsnig, H.-P. (1985). Taxonomie forstlich wichtiger Parasiten: Untersuchungen zur Struktur des männlichen Postabdomens der Raupenfliegen (Diptera, Tachinidae). Stuttgarter Beiträge zur Naturkunde Serie A (Biologie), 383, 1–137.\nVilleneuve, J. (1937). Descriptions de myodaires supérieurs. Revue de Zoologie et de Botanique Africaines, 29, 205–212.\nVilleneuve, J. (1939). Myodaires supérieurs africains (descriptions et observations). Bulletin du Musée Royal d’Histoire Naturelle de Belgique, 15(48), 1–10.\nWood, D. M. (1987) Tachinidae. In McAlpine, J. F. Peterson, B. V. Shewell, G. E. Teskey, H. J. Vockeroth, J. R., & Wood, D. M. (Eds), Manual of Nearctic Diptera. Vol. 2. Research Branch, Agriculture Canada Monograph, 28, 1193–1269.",{"EN":1182},"The Afrotropical tachinid “genus” Agaedioxenis Villeneuve is taken here as an example of the challenges faced by dipterists in classifying one of the most diverse and species rich families of organisms on Earth. Our study has revealed “two tribes hidden in one genus”, with one lineage representing a genus belonging to the tribe Goniini (Agaedioxenis) and the other representing a genus belonging to Eryciini (Eugaedioxenis gen. nov.). The two genera have been revised through an integrative approach of morphology and genetics (COI barcode sequences). The genus name Agaedioxenis replaces that of Gaedioxenis Townsend as a valid genus name. Agaedioxenis is recognized from five species consisting of two previously described species (Agaedioxenis setifrons (Villeneuve) and Agaedioxenis brevicornis (Villeneuve) both comb. nov.) and three new species (Agaedioxenis kirkspriggsi sp. nov., Agaedioxenis succulentus sp. nov., and Agaedioxenis timidus sp. nov.). Agaedioxenis propinqua (Villeneuve) is recognized as a subjective synonym of A. brevicornis (Villeneuve), syn. nov., and by First Reviser action, the latter is chosen as the senior of the two names. Eugaedioxenis gen. nov. is recognized based on two species, Eugaedioxenis haematodes (Villeneuve), type species and comb. nov., and Eugaedioxenis horridus sp. nov. All new species of both genera are described from South Africa. We further discuss how genetics, morphology, and natural history have contributed to revise the generic circumscription of Agaedioxenis, bringing about both the description of Eugaedioxenis and the revision of the suprageneric classification for these two taxa.",{"EN":1184},"Two tribes hidden in one genus: the case of Agaedioxenis Villeneuve (Diptera: Tachinidae: Exoristinae)",{"VOID":1186},"10.1007\u002Fs13127-015-0211-0","http:\u002F\u002Flink.springer.com\u002F10.1007\u002Fs13127-015-0211-0",[1189,1204,1219,1247,1259],{"id":1190,"sortIndex":121,"researcher":24,"roles":1191,"affiliations":1192,"properties":1201},"0133906c-5a64-4db1-afe7-23d2bdc8037f",[147],[1193],{"id":24,"sortIndex":102,"affiliation":1194,"properties":24},{"id":1195,"createTime":1196,"updateTime":1196,"relativeEntities":1197,"slug":24,"properties":1198,"entityType":45,"verifyStatus":23,"verifyTime":24,"verifyNote":24,"syncStatus":23,"languages":24,"translateLanguages":24,"viewCount":102},"62e2199e-16c4-46a4-873a-98a360f67958","2023-12-06T05:04:30.265+00:00",[],{"title":1199},{"VI":1200},"Department of Biological Sciences, Wright State University, Dayton, USA",{"title":1202},{"VI":1203},"Isaac S. 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B., & Makarkin, V. N. (2004). New genus of minute Berothidae (Neuroptera) from Early Eocene amber of British Columbia. Canadian Entomologist, 136, 61–76.",{"doi":1505},"10.4039\u002Fn03-043",{"id":24,"text":1507,"url":24,"identifiers":1508},"Ardila-Camacho, A. (2013). First record of beaded lacewings (Neuroptera, Berothidae) from Colombia. Zootaxa, 3669, 159–164.",{"doi":1509},"10.11646\u002FZootaxa.3669.2.7",{"id":24,"text":1511,"url":24,"identifiers":1512},"Ardila-Camacho, A., Cancino-López, R. J., Acevedo, F., & Contreras-Ramos, A. (2019). Four new species of Plega Navás, 1928 (Neuroptera: Mantispidae) from Mexico. Zootaxa, 4612, 351–372.",{"doi":1513},"10.11646\u002Fzootaxa.4612.3.3",{"id":24,"text":1515,"url":24,"identifiers":1516},"Ardila-Camacho, A., Martins, C. C., Aspöck, U., & Contreras-Ramos, A. (2021). 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Zeitschrift Der Arbeitsgemeinschaft Österreichischer Entomologen, 31, 92–96.",{},{"id":24,"text":1528,"url":24,"identifiers":1529},"Aspöck, U., & Aspöck, H. (1981). Weitere Untersuchungen an Berothiden: Berotha Walker, Isoscelipteron Costa und Asadeteva n. g. (Neuropteroidea: Planipennia). Zeitschrift Der Arbeitsgemeinschaft Österreichischer Entomologen, 33, 1–14.",{},{"id":24,"text":1531,"url":24,"identifiers":1532},"Aspöck, U., & Aspöck, H. (1982). Das genus Nosybus Navás, 1910 (Neuropteroidea: Planipennia: Berothidae). Zeitschrift Der Arbeitsgemeinschaft Österreichischer Entomologen, 34, 91–105.",{},{"id":24,"text":1534,"url":24,"identifiers":1535},"Aspöck, U., & Aspöck, H. (1984a). Das genus Nosybus Navás, 1910 (Neuropteroidea: Planipennia: Berothidae). Zeitschrift Der Arbeitsgemeinschaft Österreichischer Entomologen, 34, 91–105.",{},{"id":24,"text":1537,"url":24,"identifiers":1538},"Aspöck, U., & Aspöck, H. (1984b). Die Berothiden Australiens I: Neue Spezies des Genus Stenobiella Tillyard (Neuropteroidea: Planipennia: Berothidae). Zeitschrift Der Arbeitsgemeinschaft Österreichischer Entomologen, 36, 17–32.",{},{"id":24,"text":1540,"url":24,"identifiers":1541},"Aspöck, U., & Aspöck, H. (1984c). Die Berothiden Australiens (und Neuseelands) II: Die Genera Trichoma, Tillyard, Trichoberotha Handschin, Protobiella Tillyard und Austroberothella n. g. (Neuropteroidea: Planipennia: Berothidae). Zeitschrift Der Arbeitsgemeinschaft Österreichischer Entomologen, 36, 65–85.",{},{"id":24,"text":1543,"url":24,"identifiers":1544},"Aspöck, U., & Aspöck, H. (1985). Das Genus Lekrugeria Navás (Neuropteroidea: Planipennia: Berothidae: Berothinae). Zeitschrift Der Arbeitsgemeinschaft Österreichischer Entomologen, 37, 85–98.",{},{"id":24,"text":1546,"url":24,"identifiers":1547},"Aspöck, U., & Aspöck, H. (1987). 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