scholarly journals New species and records of Neotropical ladybirds (Coleoptera: Coccinellidae)

2021 ◽  
Vol 47 (2) ◽  
pp. 331-374
Author(s):  
Guillermo González ◽  
Jaroslav Větrovec

A review of the Neotropical Coccinellidae in the Prague Museum, also including to a lesser extent material from other collections, has led to the description of 14 new species from Brazil, Ecuador, Panama, Peru, and Venezuela, two new combinations and 16 first records for countries. The new species described are Cyrea napoensis, Dilatitibialis manaus (Brachiacanthini), Neaporia chucanti, Prodilis saopaulo, P. pastaza and P. qedi (Cephaloscymnini), Siola karpish (Chnoodini), Calloeneis veraguas (Cryptognathini), Diomus chiriqui, D. panamensis and D. sekerkai (Diomini), Toxotoma venezuelae and T. aguascalientes (Epilachnini) and Nexophallobase panamensis (Stilochotidini) nov. spp. The new combinations are Sidonis vianai (for Neorhizobius vianai González, 2013) and Neda areolata (for Neocalvia areolata Gorham, 1982) comb. nov. First country records are Azya exuta Gordon for Ecuador, Chilocorus nigrita (Fabricius) for French Guiana, Harpasus zonatus (Mulsant) for Paraguay, Chnoodes separata Mader for Paraguay, Coelaria erythrogaster Mulsant for Surinam, Sidonis vianai (González) for Brazil, Coleomegilla occulta González for Bolivia, Neda callispilota (Guerín-Méneville) for Uruguay, Epilachna bistrisignata (Mader) for Peru, Epilachna dives Erichson for Bolivia, Hyperaspis pseudodonzeli Gordon & Canepari for Ecuador and French Guiana, Menoscelis saginata Mulsant for Bolivia, Zagloba beaumonti Casey for Bolivia and Venezuela and Scymnus hamatus Gordon for Panama.

Zootaxa ◽  
2019 ◽  
Vol 4655 (1) ◽  
pp. 1-104 ◽  
Author(s):  
ALLEN F. SANBORN

The known cicada fauna of Bolivia is identified. Adusella Haupt, 1918 rev. stat. is resurrected and redescribed being elevated from junior synonym status with Odopoea Stål, 1861. Edholmbergi Delétang, 1919 rev. stat, n. syn. is elevated from junior synonymy of Odopoea and synonymized with Adusella rev. stat. Adusella insignifera (Berg, 1879) n. comb., Adusella signata Haupt, 1918 n. comb., and Adusella venturii (Distant, 1906c) n. comb. are transferred or returned to Adusella rev. stat. Carineta bilineosa Walker 1858b rev. stat., Carineta obtusa Walker 1858b rev. stat., Carineta tenuistriga Walker 1858c rev. stat. and Carineta diplographa Berg 1879 rev. stat. are removed from junior synonymy with Carineta fasciculata (Germar, 1821). Carineta obtusa rev. stat., n. syn., Carineta tenuistriga rev. stat., n. syn. and Carineta diplographa Berg 1879 rev. stat., n. syn. are considered junior synonyms of Carineta bilineosa rev. stat. Carineta limpida Torres 1948a n. syn. is shown to be a junior synonym of Carineta fasciculata. Carineta turbida Jacobi, 1907 is transferred to the genus Herrera Distant, 1905c to become Herrera turbida (Jacobi, 1907) n. comb. The genera Diceroprocta Stål, 1870, Orialella Metcalf, 1952, Quesada Distant, 1905c, and Nosola Stål, 1866a are assigned to the Guyalnina Boulard & Martinelli, 1996 within the Fidicinini Distant, 1905d. Tympanoterpes virgulata n. sp., Cracenpsaltria nana n. sp., Guyalna dasyeia n. sp., Guyalna fasciata n. sp., Guyalna polypaga n. sp., Parnisa santacruzensis n. sp., Carineta ensifera n. sp., Carineta hamata n. sp., Carineta pictilis n. sp., Carineta uncinata n. sp., Herrera concolor n. sp., Herrera freiae n. sp., Herrera melanomesocranon n. sp., Herrera phyllodes n. sp., and Herrera signifera n. sp. are described as new. The first records of Adusella insignifera (Berg, 1879) n. comb., Adusella venturii (Distant, 1906c) n. comb., Fidicina christinae Boulard & Martinelli, 1996, Fidicina ethelae (Goding, 1925), Fidicina robini Boulard & Martinelli 1996, Fidicinoides descampsi Boulard & Martinelli, 1996, Fidicinoides pauliensis Boulard & Martinelli, 1996, Fidicinoides sucinalae Boulard & Martinelli, 1996, Proarna alalonga Sanborn & Heath, 2014, Proarna bergi (Distant, 1892a), Proarna grisea (Fabricius, 1775), Proarna guttulosa (Walker, 1858b), Proarna insignis Distant, 1881a, Proarna strigicollis Jacobi, 1907, Guyalna distanti (Goding, 1925) Guyalna glauca (Goding, 1925), Guyalna platyrhina Sanborn & Heath, 2014, Guyalna viridifemur (Walker, 1850), Majeorona lutea Distant, 1906d, Carineta bilineosa Walker 1858b rev. stat., Carineta cearana Distant, 1906c, Carineta detoulgoueti Champanhet, 2001, Carineta doxiptera Walker, 1858a, Carineta maculosa Torres, 1948a, Carineta pilifera Walker, 1858c, Carineta rufescens (Fabricius, 1803), Carineta tetraspila Jacobi, 1907, and Herrera turbida (Jacobi, 1907) n. comb. are provided. The records for Adusella insignifera (Berg, 1879) n. comb. and Adusella venturii (Distant, 1906c) n. comb. are the first records of the tribe Zammarini Distant, 1905b, subtribe Zammarina Distant, 1905a, and genus Adusella, Tympanoterpes virgulata n. sp. is the first record of the genus Tympanoterpes Stål, 1861, Majeorona lutea Distant, 1906d is the first record for the genus Majeorona Distant, 1905d, Parnisa santacruzensis n. sp. is the first record of the genus Parnisa Stål, 1862a for Bolivia, specimens in the type series of Cracenpsaltria nana n. sp. represent the first record of the genus Cracenpsaltria Sanborn, 2016c in Ecuador, and the specimens of Herrera concolor n. sp., Herrera freiae n. sp., Herrera melanomesocranon n. sp., Herrera phyllodes n. sp., and Herrera signifera n. sp., and Herrera turbida (Jacobi, 1907) n. comb. and the new combinations to the genus are the first records of the genus Herrera Distant, 1905c for Bolivia, Brazil, French Guiana, and Peru. New records are provided to expand the ranges of Proarna alalonga Sanborn & Heath, 2014 and Carineta gemella to include Paraguay, the range of Dorisiana noriegai Sanborn & Heath, 2014 to include Paraguay and French Guiana, the range of Guyalna platyrhina to include Brazil, and the range of Carineta cearana to include Colombia. Previous records of Proarna bufo Distant, 1905d and Carineta fasciculata (Germar, 1821) are considered to be misidentifications P. bergi (Distant, 1892a) and Carineta bilineosa Walker 1858b rev. stat. so that P. bufo and C. fasciculata are removed from the cicada fauna of Bolivia as is Hemisciera maculipennis (de Laporte, 1832) which is shown to have been mistakenly attributed to Bolivia and Argentina. The non-Bolivian Carineta criqualicae Boulard 1986a, Carineta guianaensis Sanborn, 2011a, Carineta quinimaculata Sanborn, 2011a, and Carineta tigrina Boulard 1986a are reassigned to the genus Herrera to become Herrera criqualicae (Boulard, 1986a) n. comb., Herrera guianaensis (Sanborn, 2011a) n. comb., Herrera quinimaculata (Sanborn, 2011a) n. comb., and Herrera tigrina (Boulard, 1986a) n. comb., respectively. A discussion on the species status of Carineta fasciculata (Germar, 1821) is provided to clarify the taxon along with the new synonymy. The currently known Bolivian cicada fauna is comprised of 83 described species from 21 genera, seven tribes and three subfamilies with the new records and new species presented here increasing the known fauna by 107.5%. 


2008 ◽  
Vol 25 (3) ◽  
pp. 487-494 ◽  
Author(s):  
Gustavo R. S. Ruiz ◽  
Antonio D. Brescovit

Type specimens of some of Caporiacco's Neotropical species are revised. The taxonomy of his species from French Guiana, whose type specimens are lost, is considered. The types of Corythalia hadzji Caporiacco, 1947, Corythalia luctuosa Caporiacco 1954, Hypaeus barromachadoi Caporiacco, 1947 and Naubolus melloleitaoi Caporiacco, 1947 are redescribed.The following new synonymies are established: Freya guianensis Caporiacco,1947 = Chira spinipes (Taczanowski, 1871) syn. nov.; Hypaeus bivittatus Caporiacco, 1947 = Hypaeus barromachadoi Caporiacco, 1947 syn. nov. New combinations are:Agelista petrusewiczi Caporiacco,1947 = Noegus petrusewiczi (Caporiacco,1947) comb. nov. .;Albionella chickeringi Caporiacco, 1954 = Mago chickeringi (Caporiacco,1954) comb. nov.;Asaracus pauciaculeis Caporiacco,1947 = Mago pauciaculeis (Caporiacco, 1947) comb. nov.; Cerionesta leucomystax Caporiacco, 1947 = Sassacus leucomystax (Caporiacco, 1947) comb. nov.; Lapsias guianensis Caporiacco, 1947 = Cobanus guianensis (Caporiacco, 1947) comb. nov.; Phiale modestissima Caporiacco, 1947 = Asaracus modestissimus (Caporiacco, 1947) comb. nov. The species Noegus lodovicoi sp. nov. is also described, based on an ex-syntype of Agelista petrusewiczi. The following nominal species are considered species inquirendae: Albionella guianensis Caporiacco, 1954, Alcmena trifasciata Caporiacco, 1954, Amycus effeminatus Caporiacco, 1954, Capidava variegata Caporiacco, 1954, Corythalia variegata Caporiacco, 1954, Dendryphantes coccineocinctus Caporiacco, 1954, Dendryphantes gertschi Caporiacco, 1947, Dendryphantes spinosissimus Caporiacco, 1954, Ilargus modestus Caporiacco, 1947, Lapsias melanopygus Caporiacco, 1947 = Frigga melanopygus (Caporiacco, 1947) comb. nov., Lurio splendidissimus Caporiacco, 1954, Nagaina modesta Caporiacco, 1954, Amycus patellaris (Caporiacco, 1954), Phidippus triangulifer Caporiacco, 1954 and Tutelina iridea Caporiacco, 1954.


Phytotaxa ◽  
2015 ◽  
Vol 217 (1) ◽  
pp. 1 ◽  
Author(s):  
Damien Ertz ◽  
Adam Flakus ◽  
Magdalena Oset ◽  
Harrie J. M. Sipman ◽  
Martin Kukwa

Records of 48 species belonging to the order Arthoniales from Bolivia are presented. Cryptothecia rosae-iselae Flakus & Kukwa and Lecanactis minuta Ertz, Flakus & Kukwa are described as new to science. Thirty-seven species are reported for the first time from Bolivia, seven of which, Alyxoria apomelaena, Cryptothecia darwiniana, C. groenhartii, C. megalocarpa, Herpothallon furfuraceum, Lecanographa uniseptata, and Opegrapha subvulgata, are new to South America. This raises the number of Arthoniales known from the country up to 72. Two new combinations are proposed: Alyxoria apomelaena (A. Massal.) Ertz for Opegrapha apomelaena A. Massal. and Myriostigma napoense (Kalb & Jonitz) Kukwa for Cryptothecia napoensis Kalb & Jonitz. Cresponea melanocheiloides is the second species of the genus shown to contain a xantholepinone. Cresponea melanocheiloides is reported as new to Costa Rica and Panama, Cryptothecia megalocarpa as new to the Netherlands Antilles and Guyana and C. striata is new to Colombia, Costa Rica, French Guiana and the Netherlands Antilles. Distribution data are reported for each species, with taxonomic remarks provided for new and some problematic taxa.


Zootaxa ◽  
2020 ◽  
Vol 4814 (1) ◽  
pp. 1-136
Author(s):  
OSKAR V. CONLE ◽  
FRANK H. HENNEMANN ◽  
YANNICK BELLANGER ◽  
PHILIPPE LELONG ◽  
TONI JOURDAN ◽  
...  

The present paper describes 16 new species and one new genus from French Guiana and numerous taxonomic changes are proposed prior to the publication of a comprehensive guide to the Phasmatodea of French Guiana. The following 16 new species are described and illustrated: Phanocles procerus n. sp., Phanocloidea lobulatipes n. sp., Cladomorphus guianensis n. sp., Hirtuleius gracilis n. sp., Parastratocles rosanti n. sp., Parastratocles fuscomarginatus n. sp., Paraprisopus apterus n. sp., Paraprisopus multicolorus n. sp., Agrostia longicerca n. sp., Isagoras similis n. sp., Paragrostia brulei n. sp., Prexaspes globosicaput n. sp., Prexaspes guianensis n. sp., Dinelytron cahureli n. sp., Prisopus clarus n. sp. and Prisopus conocephalus n. sp.. The new genus Paragrostia n. gen. is established for the newly described Paragrostia brulei n. sp. and Paragrostia flavimaculata (Heleodoro, Mendes & Rafael, 2017) n. comb. the latter of which is here transferred from Agrostia Redtenbacher, 1906.                Fifty-six new combinations are proposed with species transferred to other genera: Bacteria pallidenotata Redtenbacher, 1908, is transferred to Phanocloidea Zompro, 2001 (n. comb.); Bacteria maroniensis Chopard, 1911 is transferred to Phanocles Stål, 1875 (n. comb.); Cladomorphus gibbosus (Chopard, 1911) is transferred to Hirtuleius Stål, 1875 (n. comb.); Stratocles soror Redtenbacher, 1906, Parastratocles lugubris (Redtenbacher, 1906) and Parastratocles cryptochloris (Rehn, 1904) are transferred to Brizoides Redtenbacher, 1906 (n. comb.); Stratocles xanthomela (Olivier, 1792), Stratocles forcipatus Bolívar, 1896 and Stratocles tessulatus (Olivier, 1792) are transferred to Parastratocles (n. comb.); Olcyphides cinereus (Olivier, 1792), Perliodes affinis Redtenbacher, 1906, Perliodes nigrogranulosus Redtenbacher, 1906, Perliodes sexmaculatus Redtenbacher, 1906, Isagoras rugicollis (Gray, 1835), Isagoras sauropterus Rehn, 1947, Brizoides viridipes (Rehn, 1905) and Brizoides graminea Redtenbacher, 1906 are transferred to Agrostia Redtenbacher, 1906 (n. comb.); Agrostia flavimaculata Heleodoro, Mendes & Rafael, 2017 is transferred to Paragrostia n. gen. (n. comb.); Isagoras affinis Chopard, 1911, Isagoras chocoensis Hebard, 1921, Isagoras metricus Rehn, 1947 and Isagoras schraderi Rehn, 1947 are transferred to Tenerella Redtenbacher, 1906 (n. comb.); Xerosoma glyptomerion Rehn, 1904 is transferred to Isagoras Stål, 1875 (n. comb.); Isagoras venosus (Burmeister, 1838), Paraphasma paulense Rehn, 1918 and Paraphasma quadratum (Bates, 1865) are transferred to Prexaspes Stål, 1875 (n. comb.); Prexaspes (Prexaspes) cneius (Westwood, 1859) is transferred to Tenerella Redtenbacher, 1906 (n. comb.); Prexaspes lateralis (Fabricius, 1775) is transferred to Paraphasma Redtenbacher, 1906 (n. comb.); Isagoras santara (Westwood, 1859) and Prexaspes olivaceus Chopard, 1911 are transferred to Periphloea Redtenbacher, 1906 (n. comb.); Dinelytron agrion Westwood, 1859 is transferred to Paraprisopus Redtenbacher, 1906 (n. comb.); Anarchodes atrophicus (Pallas, 1772) is transferred to Ignacia Rehn, 1904 (n. comb.); Planudes asperus Bellanger & Conle, 2013, Planudes brunni Redtenbacher, 1906, Planudes cortex Hebard, 1919, Planudes crenulipes Rehn, 1904, Planudes funestus Redtenbacher, 1906, Planudes melzeri Piza, 1937, Planudes molorchus (Westwood, 1859), Planudes paxillus (Westwood, 1859), Planudes perillus Stål, 1875, Planudes pygmaeus (Redtenbacher, 1906) and Planudes taeniatus Piza, 1944 are transferred to Isagoras Stål, 1875 (n. comb.); Prisopoides atrobrunneus Heleodoro & Rafael, 2020, Prisopoides brunnescens Heleodoro & Rafael, 2020, Prisopoides caatingaensis Heleodoro & Rafael, 2020 and Prisopoides villosipes (Redtenbacher, 1906) are transferred to Prisopus Peletier de Saint Fargeau & Serville, 1828 (n. comb.); Melophasma antillarum (Caudell, 1914), Melophasma brachypterum Conle, Hennemann & Gutiérrez, 2011, Melophasma colombianum Conle, Hennemann & Gutiérrez, 2011 and Melophasma vermiculare Redtenbacher, 1906 are transferred to Paraprisopus Redtenbacher, 1906 (n. comb.); Prexaspes (Elasia) ambiguus (Stoll, 1813), Prexaspes (Elasia) brevipennis (Burmeister, 1838), Prexaspes (Elasia) pholcus (Westwood, 1859), Prexaspes (Elasia) viridipes Redtenbacher, 1906 and Prexaspes (Elasia) vittata (Piza, 1985) are transferred to Prexaspes Stål, 1875 (n. comb.).                Twenty-six new synonymies are established: Perliodes Redtenbacher, 1906 and Chlorophasma Redtenbacher, 1906 are synonymised with Agrostia Redtenbacher, 1906 (n. syn.); Chlorophasma Redtenbacher, 1906 is synonymised with Agrostia Redtenbacher, 1906 (n. syn.); Elasia Redtenbacher, 1906 is synonymised with Prexaspes Stål, 1875 (n. syn.); Prisopoides Heleodoro & Rafael, 2020 is synonymised with Prisopus Peletier de Saint Fargeau & Serville, 1828 (n. syn.); Melophasma Redtenbacher, 1906 is synonymised with Paraprisopus Redtenbacher, 1906 (n. syn.); Bacteria crassipes Chopard, 1911 is synonymised with Bacteria pallidenotata Redtenbacher, 1908 (n. syn.); Perliodes grisescens Redtenbacher, 1906 and Metriophasma (Metriophasma) pallidum (Chopard, 1911) are synonymised with Agrostia cinerea (Olivier, 1792) (n. syn.); Perliodes nigrogranulosus Redtenbacher, 1906 and Metriophasma (Metriophasma) ocellatum (Piza, 1937) are synonymised with Isagoras rugicollis (Gray, 1835) (n. syn.); Isagoras chopardi Hebard, 1933 is synonymised with Tenerella cneius (Westwood, 1859) (n. syn.); Isagoras proximus Redtenbacher, 1906 is synonymised with Isagoras glyptomerion (Rehn, 1904) (n. syn.); Chlorophasma hyalina Redtenbacher, 1906 is synonymised with Agrostia graminea (Redtenbacher, 1906) (n. syn.); Isagoras nitidus Redtenbacher, 1906 is synonymised with Anisa flavomaculatus (Gray, 1835) (n. syn.); Prexaspes acuticornis (Gray, 1835) is synonymised with Prexaspes servillei (Gray, 1835) (n. syn.); Prexaspes nigromaculatus Chopard, 1911 is synonymised with Periphloea santara (Westwood, 1859) (n. syn.); Prexaspes (Elasia) janus Kirby, 1904 is synonymised with Paraphasma maculatum (Gray, 1835) (n. syn.); Prexaspes dictys (Westwood, 1859) is synonymised with Prexaspes brevipennis (Burmeister, 1838) (n. syn.); Parastratocles aeruginosus Redtenbacher, 1906: 107 is synonymised with Parastratocles forcipatus Bolívar, 1896 (n. syn.); Parastratocles carbonarius (Redtenbacher, 1906: 106) is synonymised with Parastratocles lugubris (Redtenbacher, 1906) (n. syn.); Prisopus spinicollis Burmeister, 1838, Prisopus spiniceps Burmeister, 1838 and Prisopus cornutus Gray, 1835 are synonymised with Prisopus ohrtmanni (Lichtenstein, 1802) (n. syn.); the genus Planudes Stål, 1875 is synonymised with Isagoras Stål, 1875 (n. syn.); Pseudophasma annulipes (Redtenbacher, 1906) is synonymised with Pseudophasma blanchardi (Westwood, 1859) (n. syn.); Ignacia appendiculatum (Kirby, 1904) is synonymised with Anarchodes atrophicus (Pallas, 1772) (n. syn.).                Isagoras obscurum Guérin-Méneville, 1838 is shown to have been erroneously synonymised with Isagoras rugicollis (Gray, 1835) and is here re-established as a valid species (rev. stat.). Pseudophasma castaneum (Bates, 1865) is re-established as a valid species here (rev. stat.).                Paraprisopus Redtenbacher, 1906 and the entire tribe Paraprisopodini are transferred to Pseudophasmatidae: Pseudophasmatinae (n. comb.).                Lectotypes are designated for Perliodes grisescens Redtenbacher, 1906, Isagoras plagiatus Redtenbacher, 1906.Neotypes are designated for Agrostia cinerea (Olivier, 1792), Prexaspes ambiguus (Stoll, 1813), Prisopus horridus (Gray, 1835) and Prisopus sacratus (Olivier, 1792). 


2020 ◽  
Author(s):  
Wei Dong ◽  
Bin Wang ◽  
Kevin D. Hyde ◽  
Eric H. C. McKenzie ◽  
Huzefa A. Raja ◽  
...  

AbstractFreshwater Dothideomycetes are a highly diverse group of fungi, which are mostly saprobic in freshwater habitats worldwide. They are important decomposers of submerged woody debris and leaves in water. In this paper, we outline the genera of freshwater Dothideomycetes with notes and keys to species. Based on multigene analyses and morphology, we introduce nine new genera, viz. Aquimassariosphaeria, Aquatospora, Aquihelicascus, Fusiformiseptata, Neohelicascus, Neojahnula, Pseudojahnula, Purpureofaciens, Submersispora; 33 new species, viz. Acrocalymma bipolare, Aquimassariosphaeria kunmingensis, Aquatospora cylindrica, Aquihelicascus songkhlaensis, A. yunnanensis, Ascagilis submersa, A. thailandensis, Bambusicola aquatica, Caryospora submersa, Dictyocheirospora thailandica, Fusiformiseptata crocea, Helicosporium thailandense, Hongkongmyces aquaticus, Lentistoma aquaticum, Lentithecium kunmingense, Lindgomyces aquaticus, Longipedicellata aquatica, Neohelicascus submersus, Neohelicomyces dehongensis, N. thailandicus, Neohelicosporium submersum, Nigrograna aquatica, Occultibambusa kunmingensis, Parabambusicola aquatica, Pseudoasteromassaria aquatica, Pseudoastrosphaeriella aquatica, Pseudoxylomyces aquaticus, Purpureofaciens aquatica, Roussoella aquatica, Shrungabeeja aquatica, Submersispora variabilis, Tetraploa puzheheiensis, T. yunnanensis; 16 new combinations, viz. Aquimassariosphaeria typhicola, Aquihelicascus thalassioideus, Ascagilis guttulaspora, A. queenslandica, A. seychellensis, A. sunyatsenii, Ernakulamia xishuangbannaensis, Neohelicascus aquaticus, N. chiangraiensis, N. egyptiacus, N. elaterascus, N. gallicus, N. unilocularis, N. uniseptatus, Neojahnula australiensis, Pseudojahnula potamophila; 17 new geographical and habitat records, viz. Aliquandostipite khaoyaiensis, Aquastroma magniostiolata, Caryospora aquatica, C. quercus, Dendryphiella vinosa, Ernakulamia cochinensis, Fissuroma neoaggregatum, Helicotruncatum palmigenum, Jahnula rostrata, Neoroussoella bambusae, N. leucaenae, Occultibambusa pustula, Paramonodictys solitarius, Pleopunctum pseudoellipsoideum, Pseudocapulatispora longiappendiculata, Seriascoma didymosporum, Shrungabeeja vadirajensis and ten new collections from China and Thailand, viz. Amniculicola guttulata, Aquaphila albicans, Berkleasmium latisporum, Clohesyomyces aquaticus, Dictyocheirospora rotunda, Flabellascoma fusiforme, Pseudoastrosphaeriella bambusae, Pseudoxylomyces elegans, Tubeufia aquatica and T. cylindrothecia. Dendryphiella phitsanulokensis and Tubeufia roseohelicospora are synonymized with D. vinosa and T. tectonae, respectively. Six orders, 43 families and 145 genera which belong to freshwater Dothideomycetes are reviewed. Of these, 46 genera occur exclusively in freshwater habitats. A world map illustrates the distribution of freshwater Dothideomycetes.


Zootaxa ◽  
2012 ◽  
Vol 3373 (1) ◽  
pp. 1 ◽  
Author(s):  
HOUHUN LI ◽  
KLAUS SATTLER

The genus Mesophleps Hübner (Lepidoptera: Gelechiidae) is revised; 54 available names (including one unjustifiedemendation), one junior primary homonym and one unavailable name were considered; type material of 44 previouslydescribed nominal species was examined. Nine new species are described: M. acutunca sp. nov., M. bifidella sp. nov., M.unguella sp. nov., M. gigantella sp. nov., M. coffeae sp. nov., M. parvella sp. nov., M. aspina sp. nov., M. truncatella sp.nov. and M. undulatella sp. nov. Two possibly new species are discussed but not formally named for lack of material.Twenty-five new combinations are introduced: M. safranella (Legrand, 1965) comb. nov., M. epichorda (Turner, 1919)comb. nov., M. tabellata (Meyrick, 1913) comb. nov., M. crocina (Meyrick, 1904) comb. nov., M. ochracella (Turati,1926) comb. nov., M. geodes (Meyrick, 1929) comb. nov., M. catericta (Meyrick, 1927) comb. nov., M. tephrastis(Meyrick, 1904) comb. nov., M. cycnobathra (Lower, 1898) comb. nov., M. tetrachroa (Lower, 1898) comb. nov., M.ochroloma (Lower, 1901) comb. nov., M. trichombra (Lower, 1898) comb. nov., M. mylicotis (Meyrick, 1904) comb. nov.,M. macrosemus (Lower, 1900) comb. nov., M. apentheta (Turner, 1919) comb. nov., M. meliphanes (Lower, 1894) comb.nov., M. chloranthes (Lower, 1900) comb. nov., M. centrothetis (Meyrick, 1904) comb. nov., M. chloristis (Meyrick,1904) comb. nov., M. argonota (Lower, 1901) comb. nov., Megacraspedus arnaldi (Turati & Krüger, 1936) comb. nov.,Aponoea cinerellus (Turati, 1930) comb. nov., Pycnobathra acromelas (Turner, 1919) comb. nov., Sarotorna mesoleuca(Lower, 1900) comb. nov., S. dentata Meyrick, 1904, comb. nov. One species, Nothris mesophracta Turner, 1919, isremoved from Mesophleps but no current genus is available. Fourteen new synonymies (one genus, 13 species-group taxa)are established: Bucolarcha Meyrick, 1929, syn. nov. of Mesophleps Hübner, [1825]; Stiphrostola longinqua Meyrick,1923, syn. nov. and Brachyacma trychota Meyrick, 1929, syn. nov. of M. ioloncha (Meyrick, 1905); Lipatia crotalariellaBusck, 1910, syn. nov. of M. adustipennis (Walsingham, 1897); Brachyacma epichorda Turner, 1919, syn. nov. of M.epiochra (Meyrick, 1886); Mesophleps pudicellus var. apicellus Caradja, 1920, syn. nov. and Mesophleps silacellus subsp.calaritanus Amsel, 1939, syn. nov. of M. silacella (Hübner, 1796); Mesophleps lala Agenjo, [1961], syn. nov. of M.corsicella (Herrich-Schäffer, 1856); Crossobela barysphena Meyrick, 1923, syn. nov. of M. trinotella Herrich-Schäffer,1856; Mesophleps orientella Nel & Nel, 2003, syn. n. and Mesophleps gallicella Varenne & Nel, 2011, syn. nov. of M.ochracella (Turati, 1926); Nothris centrothetis Meyrick, 1904, syn. nov. and Nothris chloristis Meyrick, 1904, syn. nov.of M. chloranthes (Lower, 1900); Mesophleps cinerellus Turati, 1930, syn. nov. of Aponoea obtusipalpis Walsingham,1905. One genus and one species are recalled from synonymy: Pycnobathra Lower, 1901, gen. rev., and M. ioloncha(Meyrick, 1905) sp. rev. Lectotypes are designated, in accordance with the Code, article 74.7.3, for 14 species: Gelechiapalpigera Walsingham, 1891; Paraspistes ioloncha Meyrick, 1905; Lathontogenus adustipennis Walsingham, 1897;Brachyacma epichorda Turner, 1919; Nothris crocina Meyrick, 1904; Nothris ochracella Turati, 1926; Nothris tephrastisMeyrick, 1904; Ypsolophus ochroloma Lower, 1901; Ypsolophus macrosemus Lower, 1900; Nothris centrothetis Meyrick,1904; Nothris chloristis Meyrick, 1904; Ypsolophus argonota Lower, 1901; Mesophleps arnaldi Turati & Krüger, 1936,and Mesophleps cinerellus Turati, 1930. Mesophleps is a widely distributed Old World genus, except for one New Worldspecies, with seed-feeding larvae on Cupressaceae, Cistaceae, Cruciferae (Brassicaceae), Leguminosae (Fabaceae), Rubiaceae and doubtfully Dipterocarpaceae.


2006 ◽  
Vol 56 (9) ◽  
pp. 2025-2027 ◽  

The purpose of this announcement is to effect the valid publication of the following new names and new combinations under the procedure described in the Bacteriological Code (1990 Revision). Authors and other individuals wishing to have new names and/or combinations included in future lists should send three copies of the pertinent reprint or photocopies thereof to the IJSEM Editorial Office for confirmation that all of the other requirements for valid publication have been met. It is also a requirement of IJSEM and the ICSP that authors of new species, new subspecies and new combinations provide evidence that types are deposited in two recognized culture collections in two different countries (i.e. documents certifying deposition and availability of type strains). It should be noted that the date of valid publication of these new names and combinations is the date of publication of this list, not the date of the original publication of the names and combinations. The authors of the new names and combinations are as given below, and these authors' names will be included in the author index of the present issue and in the volume author index. Inclusion of a name on these lists validates the publication of the name and thereby makes it available in bacteriological nomenclature. The inclusion of a name on this list is not to be construed as taxonomic acceptance of the taxon to which the name is applied. Indeed, some of these names may, in time, be shown to be synonyms, or the organisms may be transferred to another genus, thus necessitating the creation of a new combination.


Sign in / Sign up

Export Citation Format

Share Document