Phylogenetic and Morphological Characteristics Reveal Cryptic Speciation in Stingless Bee, Tetragonula laeviceps s.l. Smith 1857 (Hymenoptera; Meliponinae) by Kimberly Ador, Januarius Gobilik, Suzan Benedick

“…Smith 1857 has the most complicated nomenclatural history among the Tetragonula genera. The objective of this study was to investigate whether T. laeviceps s.l. individuals with worker bees are grouped in the same or nearly the same morphological characteristics and have similar COI haplotype cluster groups. …”
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La Red Internacional de Inventarios Forestales (BIOTREE-NET) en Mesoamérica: avances, retos y perspectivas futuras by L. Cayuela, L. Gálvez-Bravo, F.S. de Albuquerque, D.J. Golicher, M. González-Espinosa, N. Ramírez-Marcial, J.M. Rey Benayas, R.A. Zahawi, J.A. Meave, B.M. Benito, C. Garibaldi, I. Chan, R. Pérez Pérez, R. Field, P. Balvanera, M.A. Castillo, B.L. Figueroa-Rangel, D.M. Griffith, G.A. Islebe, D.L. Kelly, M. Olvera-Vargas, S.A. Schnitzer, E. Velazquez, G. Williams-Linera, S.W. Brewer, A. Camacho-Cruz, I. Coronado, B. de Jong, R. del Castillo, I. Granzow-de la Cerda, J. Fernández, W. Fonseca, L. Galindo-Jaimes, T.W. Gillespie, B. González-Rivas, J.E. Gordon, J. Hurtado, J. Linares, S.G. Letcher, S.A. Mangan, V.E. Méndez, V. Meza, S. Ochoa-Gaona, C.J. Peterson, V. Ruiz-Gutierrez, K.A. Snarr, F. Tun Dzul, M. Valdez-Hernández, K.M. Viergever, D.A. White, J.N. Williams, F.J. Bonet, R. Zamora

“…Se ha desarrollado un sistema para la corrección de errores tipográficos y la estandarización taxonómica y nomenclatural utilizando como referencia The Plant List (http://theplantlist.org/). …”
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Páramo Calamagrostis s.l. (Poaceae): An updated list and key to the species known or likely to occur in páramos of NW South America and southern Central America including two new s... by Steven P. Sylvester, Robert J. Soreng, William J. Bravo-Pedraza, Lia E. Cuta-Alarcon, Diego Giraldo-Cañas, Jose Aguilar-Cano, Paul M. Peterson

“…Deschampsia podophora var. mutica principally differs from var. podophora by florets lacking awns and larger habit i.e. multiple taller culms with longer and wider leaf blades forming tussocks, with inflorescences often held within sheaths. Nomenclatural changes are presented, with Deyeuxia macrostachya newly synonymised under C. macrophylla and C. pittieri, C. pubescens and Deyeuxia pubescens newly synonimised under C. planifolia. …”
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AI-guided discovery of the invariant host response to viral pandemics by Debashis Sahoo, Gajanan D. Katkar, Soni Khandelwal, Mahdi Behroozikhah, Amanraj Claire, Vanessa Castillo, Courtney Tindle, MacKenzie Fuller, Sahar Taheri, Thomas F. Rogers, Nathan Beutler, Sydney I. Ramirez, Stephen A. Rawlings, Victor Pretorius, Davey M. Smith, Dennis R. Burton, Laura E. Crotty Alexander, Jason Duran, Shane Crotty, Jennifer M. Dan, Soumita Das, Pradipta Ghosh

“…Findings: The 166-gene signature was surprisingly conserved across all viral pandemics, including COVID-19, and a subset of 20-genes classified disease severity, inspiring the nomenclatures ViP and severe-ViP signatures, respectively. …”
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Checklist of the Discomycetes (Fungi) of Patagonia, Tierra del Fuego and adjacent antarctic areas by Irma J. Gamundí, David W. Minter, Andrea I. Romero, Viviana A. Barrera, Andreina L. Giaiotti, María I. Messuti, Marina Stecconi

“…Cada uno de estos taxones (y cada sinónimo conocido) está representado por un registro separado en la Base de Datos Taxonómica y Nomenclatural. La información sobre fuentes relevantes de bibliografía fue acumulada en más de 120 registros en la Base de Datos de Bibliografía. …”
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Carpological features of Lonicera L. (Caprifoliaceae Juss.) of the flora of Ukraine by O.M. Tsarenko, O.V. Bulakh, O.V. Kolesnichenko, S.M. Hrysiuk

“…The fruits and seeds of seven species of the genus (four are introduced and the other are species of natural flora), listed in “Vascular plants of Ukraine. A nomenclatural checklist”, have been studied. Morphological features of fruits and seeds were studied under light microscope (LM, MBS-9) and scanning electron microscope (SEM, JSM-6060 LA). …”
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Printed Ladies Cloaks between culture identity and technological progress by Gihan El Gamal

“…In recent times, Women have become wearing cloak in different ages, Regardless of their affiliations and tastes ,the cloak has become an essential part of the bride's clothes closet in most Arab countries , Varied forms and types , colors and nomenclatures _ Completely different from what it was in the past _ Black cloak and a traditional folk legacies required by the customs and traditions, It has taken one pattern for a long time, But it has been changing little by little , The current research is trying to shed light on some of the basic forms of women's cloaks and inventing designs for printed ladies clocks , Keep pace with global trendy fashion lines in terms of design , materials and printing  method used in their production, And maintained at the same time on the Arab cultural identity, with computer-aided. …”
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A revision of the family Ameroseiidae (Acari, Mesostigmata), with some data on Slovak fauna by Peter Mašán

“…It contains 206 named species (138 valid species, 37 synonyms, nine unrecognizable species, 15 species previously excluded from Ameroseiidae, and seven “nomina nuda”), with details of their authorship, synonyms, nomenclatural and bibliographic details, generic placement, and morphology. …”
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Bibliometría de la sistemática biológica sobre América Latina durante el siglo XX en tres bases de datos mundiales by Layla Michán, Jorge Llorente-Bousquets

“…Of the documents, 54.6% related to new species, 15.3% dealt with morphology, 14.9% keys, 12.5% descriptions, 10.6% cases of synonymies, 6% new genera, 4.9% new geographical records, 23.6% geographical distribution, 4.2% redescriptions, and 3.6% with new nomenclatural combinations. The regions mentioned were South America with 11.9%, Central America with 4% and America (all) with 2.56%. …”
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Las principales discordancias del Mesozoico de la Cuenca Neuquina según observaciones de superficie The main unconformities of the Mesozoic of the Neuquén Basin based on surface ob... by Héctor A. Leanza

“…The obtained results lead to suggest some new ideas with regard to the evolution of the Neuquén Basin and to keep attention on still open nomenclatural problems.…”
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Filogenia de los bagres marinos (Siluriformes: Ariidae) del nuevo mundo by Ricardo Betancur Rodríguez, Arturo Acero P.

“…Las filogenias obtenidas concuerdan todas con la división de Ariidae en dos subfamilias: Ariinae y el grupo de los Galeichthyinos, el cual requiere estatus nomenclatural. Se corroboró la validez, y en gran medida la monofilia de los géneros Ariopsis, Bagre, Cathorops, Galeichthys, Potamarius y Selenaspis (incluyendo a S. proops y S. parkeri). …”
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Annotated catalogue of the Tachinidae (Insecta, Diptera) of Chile by James E. O'Hara, D. Monty Wood, Christian R. González

“…The Tachinidae (Diptera) of Chile are catalogued and information is given on distributions, name-bearing types, synonyms, nomenclatural issues, and pertinent literature. The history of tachinid collectors in Chile and authors who have contributed to the systematic knowledge of Chilean tachinids is extensively reviewed. …”
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A preliminary study of the moss genus Isopterygium in Latin America A preliminary study of the moss genus Isopterygium in Latin America by Ireland Robert R.

“…El detallado estudio nomenclatural permitió reconocer para la región siete especies: <em>Isopterygium</em></span><em><span style="font-size: 12pt; font-family: " lang="EN-US"> affusum </span></em><span style="font-size: 12pt; font-family: " lang="EN-US">Mitt., <em>I. byssobolax </em>(C. …”
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Review of Apanteles sensu stricto (Hymenoptera, Braconidae, Microgastrinae) from Area de Conservación Guanacaste, northwestern Costa Rica, with keys to all described species from M... by Jose Fernandez-Triana, James Whitfield, Josephine Rodriguez, M. Alex Smith, Daniel Janzen, Winnie Hallwachs, Mehrdad Hajibabaei, John Burns, Alma Solis, John Brown, Sophie Cardinal, Henri Goulet, Paul Hebert

“…We have used several information sources and techniques (traditional taxonomy, molecular, software-based, biology, and geography) to accelerate the process of finding and describing these new species in a hyperdiverse group such as Apanteles.The following new taxonomic and nomenclatural acts are proposed. Four species previously considered to be Apanteles are transferred to other microgastrine genera: Dolichogenidea hedyleptae (Muesebeck, 1958) comb. n., Dolichogenidea politiventris (Muesebeck, 1958) comb. n., Rhygoplitis sanctivincenti (Ashmead, 1900) comb. n., and Illidops scutellaris (Muesebeck, 1921) comb. rev. …”
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Description and phylogenetic analysis of the Calycopidina (Lepidoptera, Lycaenidae, Theclinae, Eumaeini): a subtribe of detritivores Descrição e análise filogenética de Calycopidin... by Marcelo Duarte, Robert K. Robbins

“…Johnson & Kroenlein, 1993, are nomenclaturally unavailable and polyphyletic as proposed. …”
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A catalogue of the tribe Sepidiini Eschscholtz, 1829 (Tenebrionidae, Pimeliinae) of the world by Marcin J. Kamiński, Kojun Kanda, Ryan Lumen, Jonah M. Ulmer, Christopher C. Wirth, Patrice Bouchard, Rolf Aalbu, Noël Mal, Aaron D. Smith

“…Distribution of the subtribes is illustrated and discussed. Several new nomenclatural acts are included. The generic names Phanerotomea Koch, 1958 [= Ocnodes Fåhraeus, 1870] and Parmularia Koch, 1955 [= Psammodes Kirby, 1819] are new synonyms (valid names in square brackets). …”
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Annotated and illustrated world checklist of Microgastrinae parasitoid wasps (Hymenoptera, Braconidae) by Jose Fernandez-Triana, Mark R. Shaw, Caroline Boudreault, Melanie Beaudin, Gavin R. Broad

“…Microgastrinae hosts are here considered to be restricted to Eulepidoptera, i.e., most of the Lepidoptera except for the four most basal superfamilies (Micropterigoidea, Eriocranioidea, Hepialoidea and Nepticuloidea), with all previous literature records of other insect orders and those primitive Lepidoptera lineages being considered incorrect. The following nomenclatural acts are proposed: 1) Two genera are synonymyzed under Apanteles: Cecidobracon Kieffer &amp;amp; Jörgensen, 1910, new synonym and Holcapanteles Cameron, 1905, new synonym; 2) Nine lectotype designations are made for Alphomelon disputabile (Ashmead, 1900), Alphomelon nigriceps (Ashmead, 1900), Cotesia salebrosa (Marshall, 1885), Diolcogaster xanthaspis (Ashmead, 1900), Dolichogenidea ononidis (Marshall, 1889), Glyptapanteles acraeae (Wilkinson, 1932), Glyptapanteles guyanensis (Cameron, 1911), Glyptapanteles militaris (Walsh, 1861), and Pseudapanteles annulicornis Ashmead, 1900; 3) Three new replacement names are a) Diolcogaster aurangabadensis Fernandez-Triana, replacing Diolcogaster indicus (Rao &amp;amp; Chalikwar, 1970) [nec Diolcogaster indicus (Wilkinson, 1927)], b) Dolichogenidea incystatae Fernandez-Triana, replacing Dolichogenidea lobesia Liu &amp;amp; Chen, 2019 [nec Dolichogenidea lobesia Fagan-Jeffries &amp;amp; Austin, 2019], and c) Microplitis vitobiasi Fernandez-Triana, replacing Microplitis variicolor Tobias, 1964 [nec Microplitis varicolor Viereck, 1917]; 4) Three names amended are Apanteles irenecarrilloae Fernandez-Triana, 2014, Cotesia ayerzai (Brèthes, 1920), and Cotesia riverai (Porter, 1916); 5) Seven species have their status revised: Cotesia arctica (Thomson, 1895), Cotesia okamotoi (Watanabe, 1921), Cotesia ukrainica (Tobias, 1986), Dolichogenidea appellator (Telenga, 1949), Dolichogenidea murinanae (Capek &amp;amp; Zwölfer, 1957), Hypomicrogaster acarnas Nixon, 1965, and Nyereria nigricoxis (Wilkinson, 1932); 6) New combinations are given for 318 species: Alloplitis congensis, Alloplitis detractus, Apanteles asphondyliae, Apanteles braziliensis, Apanteles sulciscutis, Choeras aper, Choeras apollion, Choeras daphne, Choeras fomes, Choeras gerontius, Choeras helle, Choeras irates, Choeras libanius, Choeras longiterebrus, Choeras loretta, Choeras recusans, Choeras sordidus, Choeras stenoterga, Choeras superbus, Choeras sylleptae, Choeras vacillatrix, Choeras vacillatropsis, Choeras venilia, Cotesia asavari, Cotesia bactriana, Cotesia bambeytripla, Cotesia berberidis, Cotesia bhairavi, Cotesia biezankoi, Cotesia bifida, Cotesia caligophagus, Cotesia cheesmanae, Cotesia compressithorax, Cotesia delphinensis, Cotesia effrena, Cotesia euphobetri, Cotesia elaeodes, Cotesia endii, Cotesia euthaliae, Cotesia exelastisae, Cotesia hiberniae, Cotesia hyperion, Cotesia hypopygialis, Cotesia hypsipylae, Cotesia jujubae, Cotesia lesbiae, Cotesia levigaster, Cotesia lizeri, Cotesia malevola, Cotesia malshri, Cotesia menezesi, Cotesia muzaffarensis, Cotesia neptisis, Cotesia nycteus, Cotesia oeceticola, Cotesia oppidicola, Cotesia opsiphanis, Cotesia pachkuriae, Cotesia paludicolae, Cotesia parbhanii, Cotesia parvicornis, Cotesia pratapae, Cotesia prozorovi, Cotesia pterophoriphagus, Cotesia radiarytensis, Cotesia rangii, Cotesia riverai, Cotesia ruficoxis, Cotesia senegalensis, Cotesia seyali, Cotesia sphenarchi, Cotesia sphingivora, Cotesia transuta, Cotesia turkestanica, Diolcogaster abengouroui, Diolcogaster agama, Diolcogaster ambositrensis, Diolcogaster anandra, Diolcogaster annulata, Diolcogaster bambeyi, Diolcogaster bicolorina, Diolcogaster cariniger, Diolcogaster cincticornis, Diolcogaster cingulata, Diolcogaster coronata, Diolcogaster coxalis, Diolcogaster dipika, Diolcogaster earina, Diolcogaster epectina, Diolcogaster epectinopsis, Diolcogaster grangeri, Diolcogaster heterocera, Diolcogaster homocera, Diolcogaster indica, Diolcogaster insularis, Diolcogaster kivuana, Diolcogaster mediosulcata, Diolcogaster megaulax, Diolcogaster neglecta, Diolcogaster nigromacula, Diolcogaster palpicolor, Diolcogaster persimilis, Diolcogaster plecopterae, Diolcogaster plutocongoensis, Diolcogaster psilocnema, Diolcogaster rufithorax, Diolcogaster semirufa, Diolcogaster seyrigi, Diolcogaster subtorquata, Diolcogaster sulcata, Diolcogaster torquatiger, Diolcogaster tristiculus, Diolcogaster turneri, Diolcogaster vulcana, Diolcogaster wittei, Distatrix anthedon, Distatrix cerales, Distatrix cuspidalis, Distatrix euproctidis, Distatrix flava, Distatrix geometrivora, Distatrix maia, Distatrix tookei, Distatrix termina, Distatrix simulissima, Dolichogenidea agamedes, Dolichogenidea aluella, Dolichogenidea argiope, Dolichogenidea atreus, Dolichogenidea bakeri, Dolichogenidea basiflava, Dolichogenidea bersa, Dolichogenidea biplagae, Dolichogenidea bisulcata, Dolichogenidea catonix, Dolichogenidea chrysis, Dolichogenidea coffea, Dolichogenidea coretas, Dolichogenidea cyane, Dolichogenidea diaphantus, Dolichogenidea diparopsidis, Dolichogenidea dryas, Dolichogenidea earterus, Dolichogenidea ensiger, Dolichogenidea eros, Dolichogenidea evadne, Dolichogenidea falcator, Dolichogenidea gelechiidivoris, Dolichogenidea gobica, Dolichogenidea hyalinis, Dolichogenidea iriarte, Dolichogenidea lakhaensis, Dolichogenidea lampe, Dolichogenidea laspeyresiella, Dolichogenidea latistigma, Dolichogenidea lebene, Dolichogenidea lucidinervis, Dolichogenidea malacosomae, Dolichogenidea maro, Dolichogenidea mendosae, Dolichogenidea monticola, Dolichogenidea nigra, Dolichogenidea olivierellae, Dolichogenidea parallelis, Dolichogenidea pelopea, Dolichogenidea pelops, Dolichogenidea phaenna, Dolichogenidea pisenor, Dolichogenidea roepkei, Dolichogenidea scabra, Dolichogenidea statius, Dolichogenidea stenotelas, Dolichogenidea striata, Dolichogenidea wittei, Exoryza asotae, Exoryza belippicola, Exoryza hylas, Exoryza megagaster, Exoryza oryzae, Glyptapanteles aggestus, Glyptapanteles agynus, Glyptapanteles aithos, Glyptapanteles amenophis, Glyptapanteles antarctiae, Glyptapanteles anubis, Glyptapanteles arginae, Glyptapanteles argus, Glyptapanteles atylana, Glyptapanteles badgleyi, Glyptapanteles bataviensis, Glyptapanteles bistonis, Glyptapanteles borocerae, Glyptapanteles cacao, Glyptapanteles cadei, Glyptapanteles cinyras, Glyptapanteles eryphanidis, Glyptapanteles euproctisiphagus, Glyptapanteles eutelus, Glyptapanteles fabiae, Glyptapanteles fulvigaster, Glyptapanteles fuscinervis, Glyptapanteles gahinga, Glyptapanteles globatus, Glyptapanteles glyphodes, Glyptapanteles guierae, Glyptapanteles horus, Glyptapanteles intricatus, Glyptapanteles lamprosemae, Glyptapanteles lefevrei, Glyptapanteles leucotretae, Glyptapanteles lissopleurus, Glyptapanteles madecassus, Glyptapanteles marquesi, Glyptapanteles melanotus, Glyptapanteles melissus, Glyptapanteles merope, Glyptapanteles naromae, Glyptapanteles nepitae, Glyptapanteles nigrescens, Glyptapanteles ninus, Glyptapanteles nkuli, Glyptapanteles parasundanus, Glyptapanteles penelope, Glyptapanteles penthocratus, Glyptapanteles philippinensis, Glyptapanteles philocampus, Glyptapanteles phoebe, Glyptapanteles phytometraduplus, Glyptapanteles propylae, Glyptapanteles puera, Glyptapanteles seydeli, Glyptapanteles siderion, Glyptapanteles simus, Glyptapanteles speciosissimus, Glyptapanteles spilosomae, Glyptapanteles subpunctatus, Glyptapanteles thespis, Glyptapanteles thoseae, Glyptapanteles venustus, Glyptapanteles wilkinsoni, Hypomicrogaster samarshalli, Iconella cajani, Iconella detrectans, Iconella jason, Iconella lynceus, Iconella pyrene, Iconella tedanius, Illidops azamgarhensis, Illidops lamprosemae, Illidops trabea, Keylimepie striatus, Microplitis adisurae, Microplitis mexicanus, Neoclarkinella ariadne, Neoclarkinella curvinervus, Neoclarkinella sundana, Nyereria ituriensis, Nyereria nioro, Nyereria proagynus, Nyereria taoi, Nyereria vallatae, Parapanteles aethiopicus, Parapanteles alternatus, Parapanteles aso, Parapanteles atellae, Parapanteles bagicha, Parapanteles cleo, Parapanteles cyclorhaphus, Parapanteles demades, Parapanteles endymion, Parapanteles epiplemicidus, Parapanteles expulsus, Parapanteles fallax, Parapanteles folia, Parapanteles furax, Parapanteles hemitheae, Parapanteles hyposidrae, Parapanteles indicus, Parapanteles javensis, Parapanteles jhaverii, Parapanteles maculipalpis, Parapanteles maynei, Parapanteles neocajani, Parapanteles neohyblaeae, Parapanteles nydia, Parapanteles prosper, Parapanteles prosymna, Parapanteles punctatissimus, Parapanteles regalis, Parapanteles sarpedon, Parapanteles sartamus, Parapanteles scultena, Parapanteles transvaalensis, Parapanteles turri, Parapanteles xanthopholis, Pholetesor acutus, Pholetesor brevivalvatus, Pholetesor extentus, Pholetesor ingenuoides, Pholetesor kuwayamai, Promicrogaster apidanus, Promicrogaster briareus, Promicrogaster conopiae, Promicrogaster emesa, Promicrogaster grandicula, Promicrogaster orsedice, Promicrogaster repleta, Promicrogaster typhon, Sathon bekilyensis, Sathon flavofacialis, Sathon laurae, Sathon mikeno, Sathon ruandanus, Sathon rufotestaceus, Venanides astydamia, Venanides demeter, Venanides parmula, and Venanides symmysta.…”
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Catalogue of Tenebrionidae (Coleoptera) of North America by Yves Bousquet, Donald B. Thomas, Patrice Bouchard, Aaron D. Smith, Rolf L. Aalbu, M. Andrew Johnston, Warren E. Steiner Jr.

“…For each name the author and year and page number of the description are provided, with additional information (e.g., type species for genus-group names, author of synonymies for invalid taxa) depending on the taxon rank. Several new nomenclatural acts are included. One new genus, Lepidocnemeplatia Bousquet and Bouchard, is described. …”
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Teorizando e pesquisando organizações contemporâneas em contextos de crises e eventos extremos / Theorizing and researching contemporary organizations in contexts of crisis and ext... by Cintia R. Oliveira, Rafael Alcadipani, Pablo I. Madariaga, Diego M. Coraiola, Maria Luisa M. Teixeira

“…In the literature on context and extreme events, there is a diversity of nomenclatures attributed to the term, generating unhelpful controversies (Hällgren et al., 2018). …”
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