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Analyses of whole genomic shotgun datasets, COI barcodes, morphology, and historical literature suggest that the following 13 butterfly species from the family Hesperiidae (Lepidoptera: Papilionoidea) in Texas, USA are distinct from their closest named relatives and therefore are described as new (type localities are given in parenthesis): Spicauda atelis Grishin, new species (Hidalgo Co., Mission), Urbanus (Urbanus) rickardi Grishin, new species (Hidalgo Co., nr. Madero), Urbanus (Urbanus) oplerorum Grishin, new species (Hidalgo Co., Mission/Madero), Telegonus tsongae Grishin, new species (Starr Co., Roma), Autochton caballo Grishin, new species (Hidalgo Co., 6 mi W of Hidalgo), Epargyreus fractigutta Grishin, new species (Hidalgo Co., McAllen), Aguna mcguirei Grishin, new species (Cameron Co., Brownsville), Polygonus pardus Grishin, new species (Hidalgo Co., McAllen), Arteurotia artistella Grishin, new species (Hidalgo Co., Mission), Heliopetes elonmuski Grishin, new species (Cameron Co., Boca Chica), Hesperia balcones Grishin, new species (Travis Co., Volente), Troyus fabulosus Grishin, new species (Hidalgo Co., Peñitas), and Lerema ochrius Grishin, new species (Hidalgo Co., nr. Relampago). Most of these species are known in the US almost exclusively from the Lower Rio Grande Valley in Texas. Nine of the holotypes were collected in 1971-1975, a banner period for butterfly species newly recorded from the Rio Grande Valley of Texas; five of them collected by William W. McGuire, and one by Nadine M. McGuire. At the time, these new species have been recorded under the names of their close relatives. A Neotype is designated for Papilio fulminator Sepp, [1841] (Suriname). Lectotypes are designated for Goniurus teleus Hübner, 1821 (unknown, likely in South America), Goniloba azul Reakirt, [1867] (Mexico: Veracruz) and Eudamus misitra Plötz, 1881 (Mexico). Several taxonomic changes are proposed. The following taxa are species (not subspecies): Spicauda zalanthus (Plötz, 1880), reinstated status (not Spicauda teleus (Hübner, 1821)), Telegonus fulminator (Sepp, [1841]), reinstated status (not Telegonus fulgerator (Walch, 1775), Telegonus misitra (Plötz, 1881), reinstated status (not Telegonus azul (Reakirt, [1867])), Autochton reducta (Mabille and Boullet, 1919), new status (not Autochton potrillo (Lucas, 1857)), Epargyreus gaumeri Godman and Salvin, 1893, reinstated status (not Epargyreus clavicornis (Herrich-Schäffer, 1869)), and Polygonus punctus E. Bell and W. Comstock, 1948, new status (not Polygonus savigny (Latreille, [1824])). Urbanus ehakernae Burns, 2014 and Epargyreus socus chota Evans, 1952 are junior subjective synonyms of Urbanus alva Evans, 1952 and Epargyreus clavicornis (Herrich-Schäffer, 1869), respectively, and Epargyreus gaumeri tenda Evans, 1955, new combination is not a subspecies of E. clavicornis.
ZooBank registration. https://zoobank.org/D5462F9E-E08D-46C6-898D-76EE7466DD19
The Chapada dos Veadeiros National Park is a conservation unit established to preserve the highest savannahs of Central Brazil and their unique biodiversity. Eriocaulaceae are a relevant and conspicuous family in such high savannahs, but its diversity is poorly known, documented solely in general lists or in isolated efforts aimed at small groups. After a structured series of field expeditions and analysis of specimens from the relevant herbaria, we provide nomenclatural novelties, a first identification key, and an illustrated checklist for the species of Paepalanthoideae (Eriocaulaceae) in the area. We recorded 42 species of Paepalanthoideae from the Chapada dos Veadeiros National Park: Actinocephalus (Körn.) Sano (2 spp.), Comanthera L.B.Sm. (1 sp.), Paepalanthus Mart. (24 spp.), and Syngonanthus Ruhland (15 spp.). Actinocephalus brevifolius Trovó & Echtern. sp. nov. and P. irwinii Trovó & Echtern. sp. nov. are newly described species and P. politus Trovó stat. et nom. nov. is a variety of P. elongatus (Bong.) Körn. raised to the species status with a new name. The generic and specific composition shows predominance of Paepalanthus and Syngonanthus, and with a low representation of Actinocephalus and Comanthera, as expected, outside of the Espinhaço Range. More than 50% of the species (22 spp.) are endemic to the area and 25 species are endemic to Central Brazil, the area being the main center of diversity for dimerous-flowered groups. The non-endemic diversity is a combination of widespread species and marginal distribution of species typical from the Amazon and southeastern savannahs. The species are unevenly distributed in the area, with their occurrence correlated to altitude, water availability, and lithology. We reinforce that the savannahs from Central Brazil are a secondary center of diversity for Eriocaulaceae, playing a central role in the conservation of an unique and irreplaceable piece of its diversity and the Cerrado biome as well.
The genus Ochodaeus in Italy: taxonomy and distribution (Coleoptera: Scarabaeoidea: Ochodaeidae)
(2020)
The author provides a taxonomic, nomenclatural and distributional review of the genus Ochodaeus Dejean, 1821 (Coleoptera: Scarabaeoidea: Ochodaeidae) in Italy. All Italian populations have been confirmed to belong to a single species, O. chrysomeloides (Schrank, 1781). After the study of a syntype, O. cychramoides Reitter, 1892, formerly considered an Italian endemic, is confirmed to be a junior synonym of O.chrysomeloides. Type material of O. chrysomeloides is believed to be destroyed, therefore a neotype is here designated and deposited at the Natural History Museum of Vienna, Austria. A lectotype is here designated for O. cychramoides and deposited in the Hungarian Natural History Museum of Budapest, Hungary. The Italian distribution of O. chrysomeloides is given in detail and illustrated by a map.
The large number of species still to be discovered in fungi, together with an exponentially growing number of environmental sequences that cannot be linked to known taxa, has fuelled the idea that it might be necessary to formally name fungi on the basis of sequence data only. Here we object to this idea due to several shortcomings of the approach, ranging from concerns regarding reproducibility and the violation of general scientific principles to ethical issues. We come to the conclusion that sequence-based nomenclature is potentially harmful for mycology as a discipline. Additionally, a classification based on sequences as types is not within reach anytime soon, because there is a lack of consensus regarding common standards due to the fast pace at which sequencing technologies develop.
Autarcontes lopezi Fisher, 1925 (Coleoptera: Buprestidae), is transferred to the genus Agrilus Curtis, 1825 (new combination). Colobogaster bella Kirsch, 1873, is transferred to the genus Chrysobothris Eschscholtz, 1829 (new combination). Ectinogonia isamarae Moore, 1994, is resurrected as the valid name for the species previously called E. obscuripennis Cobos, 1954, as the latter is unavailable as infrasubspecific. Conognatha jakobsoni Obenberger, 1928, is resurrected over C. germaini Théry in Hoscheck, 1934, as the former name has priority. Callimicra lucida Waterhouse, 1889, is resurrected as the valid name over C. hoscheki Obenberger, 1922, which has been used due to several historical errors and misinterpretations.
ZooBank registration. urn:lsid:zoobank.org:pub:651D001D-1C91-4A1A-B8BE-335BC7E7DD0F
We propose several nomenclatural changes for taxa in the lampyrid subfamilies Ototretinae, Photurinae, and Psilocladinae (Coleoptera: Lampyridae). Evidence for the correct year of description of Drilaster albicornis lateobscura (Pic, 1921) is presented. Spellings are corrected for Drilaster debilis holzi (Pic, 1914), Drilaster impustulata fukienensis (Pic, 1955), Drilaster moutoni (Pic, 1911), Drilaster pendleburyi (Pic, 1943) and Pyrogaster lunifera (Eschscholtz, 1822). We also explain the validity of the name Photuris flavicollis Fall, 1927. Fifty-eight taxa described as variations or aberrations in the subfamilies Ototretinae, Photurinae, and Psilocladinae by Delkeskamp (1977), McDermott (1966), Wittmer (1944), and Pic (1924c), are evaluated, with their availability determined based on ICZN (1999: Article 45.6).
ZooBank registration. urn:lsid:zoobank.org:pub:65697128-997F-4A52-AC9E-6860B0BF997D
Several nomenclatural changes for taxa in the firefly subfamily Luciolinae (Coleoptera: Lampyridae) are proposed. Evidence is presented to correct the year of description for Luciola dregei Motschulsky 1853 to Motschulsky 1854 when the name was ratified. We correct the authorities and years of descriptions for type species designations for the genera Delopleurus Motschulsky, 1853, and Delopyrus Motschulsky, 1853 to Motschulsky 1854 for both. All remaining taxa described as variations in the subfamily Luciolinae by McDermott (1966), are evaluated to subspecies with their availability determined based on ICZN (1999) Article 45.6.
ZooBank registration. urn:lsid:zoobank.org:pub:618A5442-2644-4E9A-BE70-07C413810DB9
We propose several nomenclatural changes for taxa in the subfamily Cladodinae and the lampyrid tribes Cratomorphini, Lamprocerini, Lampyrini, Photinini, and Pleotomini in the subfamily Lampyrinae (Coleoptera: Lampyridae). We present evidence for the correct year of description of Calotrachelum flavolineatum Pic, 1941, Diaphanes lateapicalis breveapicalis Pic, 1954, Photinus conradti Pic, 1940, and all species described by Charles Émile Blanchard. Spellings are corrected for Diaphanes lateapicalis breveapicalis Pic, 1954, Diaphanes latipennis dartevillei Pic, 1952, Diaphanes longecarinatus Pic, 1955, Diaphanes moultoni latemarginatus Pic, 1938, Lampyris olivieriana von Heyden, 1890, and Photinus reductemarginalis Pic, 1941. We propose Lucidota puertoestrellaensis Keller and Martin nomen novum to replace Lucidota boliviana Pic, 1927, and Photinus laticollis brasiliensis Keller and Martin nomen novum for Photinus laticollis latior Pic, 1941. Seventy taxa described as variations or aberrations in the tribes Cratomorphini, Lamprocerini, Lampyrini, Photinini, and Pleotomini in the subfamily Lampyrinae by McDermott (1966), are evaluated to subspecies with their availability determined based on ICZN (1999: Article 45.6). Photinus motschulskyi Zaragoza-Caballero, Zurita-Garcia, and Ramírez-Ponce, 2023 is synonymized under Photinus intercalatus Gemminger, 1870. Lastly, we correct the type species of the genus Lucidina Gorham, 1833, and address the dates of publication for fireflies described by Blanchard.
ZooBank registration. urn:lsid:zoobank.org:pub:DCD31B02-DF17-4115-A9A8-A6CBB02D8684
A synthesis of the Phaeogenini occurring in the Afrotropical region is provided. Three species are newly described: Centeterichneumon nambi Dal Pos, Diller & Di Giovanni sp. nov. from Uganda, Chauvinia ganota Claridge sp. nov. from Kenya, and Kibalus nonnaritae Dal Pos & Di Giovanni sp. nov. from Uganda. Heterischnus mfongosi Rousse & van Noort, 2013 is newly recorded for Kenya and Tanzania and the male of the species is diagnosed for the first time. Also, the female of Arearia oxymoron Rousse & van Noort, 2013 is diagnosed for the first time from one of the paratype localities. Lusius tenuissimus (Heinrich, 1938) and Chauvinia nyanga Rousse & van Noort, 2013 are recorded for the first time for Uganda and Kenya, respectively. In addition, new localities are given for Chauvinia nitida (Heinrich, 1938), Heterischnus olsoufieffi (Heinrich, 1938) and Hoplophaeogenes curticornis Heinrich, 1938. A new combination, Nesostenodontus mkomazi (Rousse & van Noort, 2013) comb. nov., is proposed to accommodate Heterischnus mkomazi. An updated key to the Afrotropical genera of Phaeogenini and keys to the Afrotropical species of the genera Arearia Seyrig, Centeterichneumon Heinrich, Chauvinia Heinrich, Heterischnus Heinrich, Hoplophaeogenes Heinrich, Kibalus Rousse, van Noort & Diller, and Lusius Tosquinet are provided. Updated online Lucid keys to genera and species are available from http://www.waspweb.org.
Rotföhrenwälder werden bereits seit Beginn der vegetationskundlichen Forschung immer wieder untersucht, eine befriedigende soziologische Klassifikation wurde jedoch bis heute kaum erreicht. Die vorliegende Arbeit beinhaltet eine syntaxonomische Neubearbeitung der Rotföhrenwälder in Österreich. 1372 Einzelaufnahmen aus Österreich und den angrenzenden Gebieten Deutschlands, Tschechiens und Italiens wurden dazu verarbeitet. Eine TWINSPAN-Klassifikation des Gesamtdatensatzes führte zu folgenden Ergebnissen:
Es werden auch weiterhin drei Haupttypen von Rotföhrenwäldern unterschieden, nämlich kontinentale inneralpische Hauhechel-Rotföhrenwälder (Ononido-Pinion), Schneeheide-Rotföhrenwälder über Karbonatgestein (Erico-Pinion) sowie bodensaure Moos-Rotföhrenwälder (Dicrano-Pinion). Aufgrund der floristischen Verwandtschaft von Erico-Pinion und Ononido-Pinion (früher Klasse Pulsatillo-Pinetea) werden nur noch zwei Klassen unterschieden (Erico-Pinetea, Vaccinio-Piceetea). Innerhalb der drei Verbände lassen sich sechs Assoziationen unterscheiden, wobei die Karbonat-Schneeheide-Rotföhrenwälder wegen des Fehlens von guten Charakterarten in nur einer Assoziation Erico-Pinetum sylvestris dargestellt werden; die Assoziation werden in acht Subassoziationen.
Sämtliche Syntaxa werden ausführlich beschrieben und nomenklatorisch revidiert. Eine synoptische Tabelle sowie Bestimmungsschlüssel für die Assoziationen und Subassoziationen sind beigefügt.
The firefly species described by Carl Linnaeus in 1758 and 1767 (Coleoptera: Lampyridae) were checked to determine the actual dates of publication. Nine out of twelve species were originally described in 1758 and not in 1767 as published in the majority of firefly literature. Lampyris hespera Linnaeus, 1767 as a junior synonym of Aspisoma lampyris (Linnaeus, 1758) is established.
ZooBank registration. urn:lsid:zoobank.org:pub:C04B88B3-DDBF-4878-B43E-71642AFC8AAA
Nomenclatural changes are proposed and herein implemented for several beetles in the family Lampyridae (Coleoptera). Corrections of authorship are proposed for Psilocladus marginatus (Lewis), Psilocladus ruficollis (Kiesenwetter), and Dryptelytra fulvipennis E. Olivier. Dates of publication are corrected for Magnoculus marginatus (Guérin-Méneville), Psilocladus calvus Kirsch, Psilocladus peruvianus Kirsch, and Vesta vitellinothorax (Perty) a synonym of Vesta thoracica (G. A. Olivier). "Dodacles grandjeani E. Olivier" is found to be a nomen nudum, which actually refers to Dryptelytra grandjeani (E. Olivier).
Diospyros L. is a large genus of flowering plants predominantly distributed in the tropics. It comprises over 700 species globally and around 300 are believed to occur in South-East Asia. Many species are economically important and exploited for the production of ebony wood and persimmons, yet taxonomic information on the genus is incomplete and inconsistent due to its morphological and nomenclatural complexity. Revisions of Diospyros in continental and insular South-East Asia were conducted independently by different authors, occasionally with different names used for the same species, or different species being given the same name in different countries. During our ongoing study of the genus Diospyros in Indochina (Cambodia, Laos, Thailand and Vietnam), we identified several such instances. Here, we clarify the most commonly misidentified species, including 1) D. apiculata Hiern, D. strigosa Hemsl. and D. tamiriensis Lecomte; 2) D. bejaudii Lecomte and D. retrofracta Bakh.; 3) D. dictyoneura Hiern and D. hasseltii Zoll.; 4) D. borneensis Hiern and D. fecunda H.R.Fletcher. Lectotypifications are also made for D. brachiata King & Gamble var. lanceolata H.R.Fletcher, D. fecunda, D. similis Craib and D. strigosa.
Nomenclatural changes are proposed and herein implemented for several firefly taxa in the family Lampyridae (Coleoptera). Dates of publication are corrected for Lampyris brutia Costa, 1882, Diaphanes costulatus (Kolbe, 1897), Diaphanes fraternus (Kolbe, 1897), Diaphanes kilimanus (Kolbe, 1897), Diaphanes breviusculus (Kolbe, 1897) (a junior synonym of Diaphanes notaticollis E. Olivier), Diaphanes piligerus (Kolbe, 1897), Diaphanes planitianus (Kolbe, 1897), Diaphanes volkensi (Kolbe, 1897) (a junior synonym of Diaphanes rugicollis (Fairmaire)), Diaphanes signaticollis Pic, 1951, Diaphanes ugandanus (Kolbe, 1897), Pyrocoelia iwasakii (Matsumura, 1918), Pyrocoelia tappana (Matsumura, 1918), Lamprocera latreillei (Kirby, 1818), Tenaspis semifusca (Gorham, 1881), Lucernuta savignii (Kirby, 1818), Aspisoma candellarium Reiche, 1845, Aspisoma roseiventer (E. Olivier, 1888), Pyractomena Melsheimer, 1846, Pyractomena flavocincta LeConte, 1852 (a junior synonym of Pyractomena angulata (Say)), Pyractomena angustata LeConte, 1852, and Pyractomena lucifera Melsheimer, 1846.
A new genus and new species of potamid crab, Gurumon gurumayum gen. et sp. nov., are described from the Arunachal Pradesh State of northeastern India. Gurumon gen. nov. has affinities with Abormon Mitra, Pati & Ng, 2021, Pararanguna Dai & Chen, 1985, and some species of Potamiscus Alcock, 1909, but the new genus can easily be differentiated from them mainly by its low external orbital angle, the relatively stouter exopod of the third maxilliped, and the relatively broader male pleonal somite 6. Their male first gonopods are also different from each other. Counting Gurumon gurumayum gen. et sp. nov., India is currently known for ten genera and 24 species of potamiscine freshwater crabs, and Arunachal Pradesh for eight genera and 11 species of these crabs. The current nomenclatural problems with Potamiscus are also discussed.
Die in Europa vorkommenden Sommergrünen Brombeeren (Rubus subgenus Rubus sectio Rubus subsectio Rubus) werden in vier Serien untergliedert: Series Nessenses H. E. Weber ser. nov. (Typus: Rubus nessensis Hall), Series Rubus ser. nov. (Typus: Rubus fruticosus L. = R. plicatus Weihe & Nees), Series Canadenses (L.H. Bailey) H. E.Weber ser. nov. (Typus: Rubus canadensis L.) und Series Alleghenienses (L. H. Bailey) H. E. Weber ser. nov. (Typus: Rubus allegheniensis Porter). Die Series Rubus wird in zwei Subserien unterteilt: Subseries Rubus (Typus: Rubus fruticosus L.) subser. nov. und Subseries Subrhamnifolii (Focke) H. E. Weber subser. nov. (Typus: Rubus montanus Wirtgen = R. senticosus Koehler ex Weihe). Die Taxonomie und Nomenklatur dieser infragenerischen Taxa sind behandelt.
Type specimens of Oedionychina Chapuis, 1875 described by Fabricius from the Kiel collection are examined and illustrated. Lectotypes are designated for the following species: Chrysomela albicollis Fabricius, 1787; Chrysomela nobilitata Fabricius, 1787; Chrysomela quadrifasciata Fabricius, 1787; Chrysomela quadriguttata Fabricius, 1781; Galleruca atomaria Fabricius, 1801; Galleruca decemguttata Fabricius, 1801; Galleruca fasciata Fabricius, 1798; Galleruca humeralis Fabricius, 1801; Galleruca lunata Fabricius, 1801; Galleruca nitida Fabricius, 1801; Galleruca obsoleta Fabricius, 1801; Galleruca petaurista Fabricius, 1801; Galleruca quadrinotata Fabricius, 1798; Galleruca sellata Fabricius, 1801. The species status is restored for Chrysomela quadriguttata Fabricius, 1781 and Alagoasa areata (Germar, 1824) comb. nov. The following new combinations are proposed: Phenrica quadriguttata (Fabricius, 1781), Asphaera nitida (Fabricius, 1801), Phenrica obsoleta (Fabricius, 1801), Alagoasa areata areata (Germar, 1824), Alagoasa areata decempunctata (Latreille, 1833), Alagoasa areata escuintla Bechyné, 1955, Alagoasa areata macromela Bechyné, 1958, Alagoasa areata praecessa Bechyné, 1959, Alagoasa areata recuperata Bechyné, 1959; all comb. nov. New placement: Galleruca avicenniae Fabricius, 1792 is removed from Alticini and placed in Galerucini incertae sedis; Galleruca trifasciata Fabricius, 1801 is removed from Chrysomelidae and placed in genus Ora Clark, 1865 (Scirtidae Fleming, 1821).
Initial analyses of DNA barcode data from Norwegian populations attributed to the water mite Lebertia porosa Thor, 1900 revealed large genetic divergence and potentially cryptic species-level diversity. We used one mitochondrial (COI) and two nuclear markers (18S and 28S) as well as comparative morphological analysis to redefine Lebertia porosa, and to further investigate the species boundaries of Norwegian populations of its close relatives. Our results show that Lebertia porosa, as currently defined, consists of multiple species that can be separated by molecular and morphological characteristics. Although we document the presence of the endosymbiotic bacteria Wolbachia in two out of eight screened genetic lineages, we find no evidence of intraspecific genetic divergence caused by Wolbachia infections. The assignment of one of the genetic lineages to the nominal species could be made through morphological comparisons of specimens from the L. porosa type locality with the syntypes of L. obscura Thor, 1900. Thus, the diagnosis of L. porosa is emended and a neotype is defined. Two of the remaining genetic lineages could be assigned to existing names previously regarded as junior synonyms of L. porosa, namely L. obscura (lectotype defined here) and L. gibbosa Lundblad, 1926, which are both redescribed. The outstanding genetic lineages are unnamed, but from our work we conclude that the taxa Lebertia porosa britannica Thor, 1906, L. porosa dorsalis Thor, 1906, and L. porosa italica Thor, 1906 are nomina dubia that cannot be considered junior synonyms of L. porosa as proposed by K. Viets (1956). We also consider L. vigintimaculata Thor, 1900 a nomen dubium, probably identical to L. obscura.
A century and a half since the time of Hewitson, we are experiencing a renaissance in species discovery fueled by whole genome sequencing. A large-scale genomic analysis of Hesperiidae Latreille, 1809 (Lepidoptera), including primary type specimens, reveals a deluge of species new to science. One hundred of them (one in a new genus) are described here from the New World (type localities are given in parenthesis): Drephalys (Drephalys) diovalis Grishin, new species (Ecuador: Napo), Euriphellus panador Grishin, new species (Ecuador: Esmeraldas), Euriphellus panamicus Grishin, new species (Panama: Panama), Cecropterus (Thorybes) viridissimus Grishin, new species (Ecuador: Zamora-Chinchipe), Cecropterus (Murgaria) dariensis Grishin, new species (Panama: Darien), Urbanus (Urbanus) mericuti Grishin, new species (Ecuador: Napo), Telegonus (Telegonus) pastus Grishin, new species (Panama: Panama), Autochton (Autochton) dora Grishin, new species (Ecuador: Pastaza), Astraptes centralis Grishin, new species (Panama: Colón), Aguna claxonica Grishin, new species (Ecuador: Napo), Aguna esmeralda Grishin, new species (Ecuador: Esmeraldas), Aguna lata Grishin, new species (Guyana), Ridens angulinea Grishin, new species (Peru: Cuzco), Pythonides lera Grishin, new species (Peru: Cuzco), Pythonides latemarginatus Grishin, new species (Panama: Panama), Gindanes variegatus Grishin, new species (Brazil: Mato Grosso), Milanion (Milanion) virga Grishin, new species (Brazil: Rondônia), Milanion (Milanion) furvus Grishin, new species (Panama: Panama), Milanion (Milanion) laricus Grishin, new species (Ecuador: Napo), Charidia ronda Grishin, new species (Brazil: Rondônia), Pseudodrephalys tinas Grishin, new species (Peru: Loreto), Pseudodrephalys argus Grishin, new species (Suriname: Para), Achlyodes calvus Grishin, new species (Brazil: Santa Catarina), Spioniades artemis Grishin, new species (Panama: Panama), Spioniades artemidoides Grishin, new species (Brazil: Santa Catarina), Myrinia orieca Grishin, new species (Ecuador: Orellana), Myrinia aragua Grishin, new species (Venezuela: Aragua), Myrinia maculosa Grishin, new species (Guatemala), Myrinia manchada Grishin, new species (Guyana), Polyctor (Fenops) lamperus Grishin, new species (Panama: Darien), Nisoniades (Nisoniades) lutum Grishin, new species (Mexico: Guerrero. ), Bolla (Stolla) vena Grishin, new species (Venezuela: Aragua), Staphylus (Vulga) vula Grishin, new species (Mexico: Veracruz), Staphylus (Vulga) vulga Grishin, new species (Panama: Darien), Staphylus (Staphylus) rotundalus Grishin, new species (Ecuador: Napo), Staphylus (Staphylus) yucatanus Grishin, new species (Mexico: Quintana Roo/Yucatan), Heliopetes (Heliopetes) lana Grishin, new species (Guatemala), Canesia ella Grishin, new species (Venezuela: Barinas), Paches (Paches) loxeca Grishin, new species (Ecuador: Morona-Santiago), Clito congruens Grishin, new species (Panama: Colón), Cycloglypha corax Grishin, new species (Brazil: Rio de Janeiro), Festivia peruvia Grishin, new species (Peru: Huánuco), Decinea notata Grishin, new species (Ecuador: Napo), Pompeius fuscus Grishin, new species (Brazil: Minas Gerais), Vernia clara Grishin, new species (Panama: Chiriquí), Oligoria (Oligoria) obtena Grishin, new species (Ecuador: Napo), Thespieus mandal Grishin, new species (Brazil: Rio de Janeiro), Psoralis (Saniba) magnamacus Grishin, new species (Panama: Darien), Alychna ayonis Grishin, new species (Ecuador: Napo), Wahydra banios Grishin, new species (Ecuador: Tungurahua), Wahydra cuzcona Grishin, new species (Peru: Cuzco), Cynea (Cynea) aureofimbra Grishin, new species (Ecuador), Cynea (Nycea) quada Grishin, new species (Ecuador: Napo), Cynea (Quinta) achirae Grishin, new species (Mexico: Tamaulipas), Eutus amazonicus Grishin, new species (Peru: Madre de Dios), Eutus incus Grishin, new species (Peru: Cuzco), Eutus septemaculatus Grishin, new species (Brazil: Mato Grosso), Godmia viridicapita Grishin, new species (Ecuador: Napo), Rhomba pulla Grishin, new species (Peru: Cuzco), Niconiades victoria Grishin, new species (Mexico: Tamaulipas), Lancephallus purpurus Grishin, new genus and new species (Guyana), Mnasicles (Remella) ecua Grishin, new species (Ecuador: Pichincha), Amblyscirtes (Amblyscirtes) aeratus Grishin, new species (Mexico: Oaxaca), Amblyscirtes (Mastor) chrysoplea Grishin, new species (Mexico: Oaxaca), Amblyscirtes (Mastor) chrysomisa Grishin, new species (Mexico: Chiapas), Amblyscirtes (Flor) meridus Grishin, new species (Mexico: Veracruz), Rectava chiriquensis Grishin, new species (Panama: Chiriquí), Cobalopsis adictys Grishin, new species (Panama: Veraguas), Cymaenes melaporphyrus Grishin, new species (Mexico: San Luis Potosí), Lerema (Morys) ecuadorica Grishin, new species (Ecuador: Pichincha), Saturnus obscurior Grishin, new species (Panama: Darien), Cantha zoirodicta Grishin, new species (Peru: Madre de Dios), Cantha meiodicta Grishin, new species (Peru: Madre de Dios), Phlebodes duplex Grishin, new species (Guatemala: Cayuga), Lychnuchus (Enosis) valle Grishin, new species (Colombia: Valle), Eutychide ochoides Grishin, new species (Peru: Cuzco), Dion bora Grishin, new species (Panama: Darien), Dion occida Grishin, new species (Peru: Madre de Dios), Eprius (Eprius) veledinus Grishin, new species (Ecuador: Pichincha), Radiatus panamensis Grishin, new species (Panama: Panama), Pheraeus pulcher Grishin, new species (Peru: Madre de Dios), Callimormus rades Grishin, new species (Panama: Panama), Gubrus lubens Grishin, new species (Ecuador: Loja), Ludens labens Grishin, new species (Panama: Darien), Rigga isa Grishin, new species (Ecuador: Napo), Flaccilla lactea Grishin, new species (Peru: Cuzco), Falga athena Grishin, new species (Panama: Darien), Panoquina jay Grishin, new species (Peru: Loreto), Calpodes salianus Grishin, new species (Peru: Madre de Dios), Calpodes stingo Grishin, new species (Ecuador: Sucumbíos), Aides nobra Grishin, new species (Panama: Colón), Thracides pavo Grishin, new species (Mexico: Tabasco), Talides eluta Grishin, new species (Peru: Cuzco), Talides laeta Grishin, new species (Peru: Cuzco), Neoxeniades angustior Grishin, new species (Brazil: Rio de Janeiro), Damas zea Grishin, new species (Guyana), Tromba xantha Grishin, new species (Mexico: Veracruz), Perichares fura Grishin, new species (Ecuador: Pichincha), Carystoides (Balma) goliath Grishin, new species (Colombia: Valle), and Agathymus galeana Grishin, new species (Mexico: Nuevo Leon). Additionally, we present evidence to support 22 taxa as species (not subspecies or synonyms) and synonymize one genus and four species. Namely, the following taxa are species: Milanion pilta Evans, 1953 (not Milanion pilumnus Mabille and Boullet, 1917), Milanion latior Mabille and Boullet, 1917 (not a synonym of Milanion marciana Godman and Salvin, 1895), Charidia pilea Evans, 1953, and Charidia pocus Evans, 1953 (not Charidia lucaria (Hewitson, 1868)), Paches (Paches) gloriosus Röber, 1925 and Paches (Paches) loxana Evans, 1953 (not Paches (Paches) loxus (Westwood, 1852)), Spioniades anta Evans, 1953 (not Spioniades abbreviata (Mabille, 1888)), Decinea onasima (Hewitson, 1877) and Decinea formosus (Hayward, 1940) (not Decinea dama (Herrich-Schäffer, 1869)), Thespieus guerreronis (Dyar, 1913) (not Thespieus dalman (Latreille, [1824])), Cynea (Nycea) erebina (Möschler, 1879) and Cynea (Nycea) cleochares (Mabille, 1891) (not Cynea (Cynea) diluta (Herrich-Schäffer, 1869)), Amblyscirtes (Mastor) repta Evans, 1955 (not Amblyscirtes (Flor) florus (Godman, 1900)), Saturnus tiberius (Möschler, 1883), Saturnus conspicuus (E. Bell, 1941), Saturnus meton (Mabille, 1891), and Saturnus obscurus (E. Bell, 1941) (not Saturnus reticulata (Plötz, 1883)), Phlebodes sifax Evans, 1955 (not Phlebodes campo (E. Bell, 1947)), Eutychide ochus Godman, 1900 and Eutychide rogersi (Kaye, 1914) (not a subspecies and a synonym, respectively, of Eutychide subcordata (Herrich-Schäffer, 1869)), Falga mirabilis Evans, 1955, Falga jacta Evans, 1955, and Falga ombra Evans, 1955 (not Falga jeconia (A. Butler, 1870)); and the following taxa are junior subjective synonyms: Libra Evans, 1955 (of Phemiades Hübner, [1819]), Papilio clito Fabricius, 1787 of Milanion hemes hemes (Cramer, 1777), Pamphila hycsos Mabille, 1891 of Cynea (Nycea) erebina (Möschler, 1879), Hesperia olympia Plötz, 1882 of Eutychide subcordata (Herrich-Schäffer, 1869), and Hesperia ocrinus Plötz, 1882 of Aides aegita (Hewitson, 1866). Furthermore, we propose new combinations for genus-species: Lychnuchus (Enosis) ponka (Evans, 1955) (not Thoon Godman, 1900), and species-subspecies: Charidia pocus mayo Evans, 1953 (not Charidia lucaria (Hewitson, 1868)), Decinea onasima boliviensis (E. Bell, 1930) (not Decinea dama (Herrich-Schäffer, 1869)), Cynea (Nycea) erebina somba Evans, 1955 (not Pamphila hycsos Mabille, 1891), Saturnus tiberius suffuscus (Hayward, 1940) (not Saturnus reticulata (Plötz, 1883)), and Falga mirabilis odol Evans, 1955 (not Falga jeconia (A. Butler, 1870)). Then, Milanion pilumnus var. hemestinus Mabille and Boullet, 1917 is a junior subjective synonym of Milanion pilumnus pilumnus Mabille and Boullet, 1917, not of Milanion leucaspis (Mabille, 1878). Lectotypes are designated for nine taxa (names in original combinations below): Pellicia bromias Godman and Salvin, 1894 (Mexico: Veracruz, Atoyac), Nisoniades perforata Möschler, 1879 (Colombia), Helias ascalaphus Staudinger, 1876 (central Panama), Pamphila hycsos Mabille, 1891 (Colombia), Amblyscirtes fluonia Godman, 1900 (Mexico: Guerrero, Xocomanatlan), Mastor anubis Godman, 1900 (Mexico: Guerrero, Omiltemi), Eutychide ochus Godman, 1900 (Mexico: Veracruz, Atoyac), Cobalus subcordata Herrich-Schäffer, 1869 (Southeast Brazil), and Thracides xanthura Godman, 1901 (Panama: Chiriquí Province, Bugaba). A neotype is designated for Eudamus briccius Plötz, 1881 (Guyana: Iwokrama Forest).
ZooBank registration. urn:lsid:zoobank.org:pub:ACDF923B-906D-460E-9707-259E0ECDBCA8
The classification of the superfamily Psylloidea is revised to incorporate findings from recent molecular studies, and to integrate a reassessment of monophyla primarily based on molecular data with morphological evidence and previous classifications. We incorporate a reinterpretation of relevant morphology in the light of the molecular findings and discuss conflicts with respect to different data sources and sampling strategies. Seven families are recognised of which four (Calophyidae, Carsidaridae, Mastigimatidae and Triozidae) are strongly supported, and three (Aphalaridae, Liviidae and Psyllidae) weakly or moderately supported. Although the revised classification is mostly similar to those recognised by recent authors, there are some notable differences, such as Diaphorina and Katacephala which are transferred from Liviidae to Psyllidae. Five new subfamilies and one new genus are described, and one secondary homonym is replaced by a new species name. A new or revised status is proposed for one family, four subfamilies, four tribes, seven subtribes and five genera. One tribe and eight genera / subgenera are synonymised, and 32 new and six revised species combinations are proposed. All recognised genera of Psylloidea (extant and fossil) are assigned to family level taxa, except for one which is considered a nomen dubium.
A taxonomic review of tenebrionid platyopoid genera of the subfamily Pimeliinae from Eastern Europe, Central Asia, Afghanistan, Iran and Pakistan is given. This group of taxa was known before 1994 as the tribe Platyopini Motschulsky, 1849, which is now interpreted as a junior synonym of Pimeliini Latreille, 1802. The group is different from other Pimeliini in having dorso-lateral eyes, located above the level of the genae, and it includes the following ultrapsammophilic genera at least from Central and Southern Asia: Apatopsis Semenov, 1891, Habrochiton Semenov-Tjan-Shansky, 1907, Habrobates Semenov, 1903 [= Kawiria Schuster, 1935 syn. nov.], Dietomorpha Reymond, 1938, Przewalskia Semenov, 1893, Mantichorula Reitter, 1889, Platyope Fischer von Waldheim, 1820 [= Homopsis Semenov, 1893 syn. nov.], Earophanta Semenov, 1903. These genera are distributed in almost all large deserts of Palaearctic Asia: Karakum, Kyzylkum, Muyunkum, Taklamakan, Gobi, Registan, Dasht-e-Kawir, Dasht-e-Lut, as well as in other arid and semi-arid sandy landscapes from European Russia to the south of Eastern Siberia. The group of platyopoid genera is polyphyletic. We propose at least two monophyletic branches: the Habrobates genus group (the first four genera mentioned above), which represents the subtribe Habrobatina Nabozhenko & S. Chigray subtrib. nov. and the Platyope genus group (latter four genera) within the nominotypical subtribe. A new species is described from Pakistan (Balochistan): Dietomorpha gonzalesi S. Chigray & Nabozhenko sp. nov. Platyope granulata Fischer von Waldheim, 1820 is recorded for Kazakhstan for the first time. The following synonymy is resurrected: Apatopsis grombczewskii Semenov, 1890 = Apatopsis conradti Semenov, 1890, syn. resurr. Two new combinations resulting from the synonymy of genera are given: Habrobates gabrieli Schuster, 1935 comb. nov. (from Kawiria), Platyope grumi Semenov, 1893 comb. nov. (from Homopsis). Lectotypes are designated for the following taxa: Apatopsis grombczewskii (Semenov, 1891), Apatopsis conradti Semenov, 1891, Habrochiton vernus Semenov-Tjan-Shansky, 1907, Habrobates vernalis Semenov, 1903, Kawiria gabrieli Schuster, 1935, Platyope dilatata Reitter, 1887; Mantichorula semenowi Reitter, 1889, Mantichorula grandis Semenov, 1893, Homopsis grumi Semenov, 1893, Platyope serrata Semenov, 1893, Platyope planidorsis Reitter, 1889, Platyope tomentosa Semenov, 1893. Additional information for type specimens studied by the authors is given for Habrochiton primaeveris Semenov-Tjan-Shansky, 1907 (holotype), Habrobates vejisovi Kelejnikova, 1977, Platyope ordossica Semenov-Tjan-Shansky, 1907 (holotype), Earophanta autumnalis Semenov, 1903 (holotype, junior synonym of E. planidorsis Reitter, 1889), Earophanta loudoni Semenov, 1903 (holotype, junior synonym of Earophanta pilosissima Reitter, 1895), Earophanta pubescens Skopin, 1960 (holotype, paratypes), Earophanta beludzhistana Bogatchev, 1957 (holotype).
A review of the genus Stratiomys from India is presented. The new species Stratiomys brunettii sp. nov. is described based on male and female specimens collected from the Kashmir Himalayas. The only other congener previously recorded in India, Stratiomys approximata, is redescribed. A key to the species is presented.
As a preliminary step towards a more intensive research on the diversity of macromycetes in Greece, an updated check-list of the Greek mycoflora is presented together with information on the host-substrates and geographic occurrence. The data originated from a thorough literature search and the authors' field observations. In total, 58 families, 214 genera and 811 species of fungi are recorded belonging to Basidiomycetes. The systematics and nomenclature of the relative bibliography have been updated and suitably revised. The large gaps in our knowledge on the existence and distribution of higher fungi in Greece are emphasized.