A catalogue of the types of Platygastridae (Hymenoptera, Platygastroidea) at the Muséum national d’Histoire naturelle, Paris, with brief notes on the history of the collection

Zootaxa ◽  
2010 ◽  
Vol 2358 (1) ◽  
pp. 1 ◽  
Author(s):  
DAVID G. NOTTON

The types of 42 nominal species of Platygastridae (Platygastroidea) in the collection of the Muséum national d’Histoire naturelle, Paris are catalogued. One new combination is established: Amblyaspis sylvicola (Risbec, 1950). The name Fidiobia hofferi Kozlov, 1978 is reinstated as a valid, available name. Brief notes are provided on the collections and type material of Joseph-Étienne Giraud, Jean-Jacques Kieffer, Paul Marchal and Jean Risbec.

Zootaxa ◽  
2012 ◽  
Vol 3245 (1) ◽  
pp. 30 ◽  
Author(s):  
JAVIER H. SIGNORELLI ◽  
GUIDO PASTORINO

The worldwide distributed family Mactridae Lamarck, 1809, is well represented in the western Atlantic Ocean. An ex-haustive literature research revealed 54 nominal species from the Brazilian coast. The study was done using morphologicalcharacters of shell and in some cases mantle cavity organs. All type material was examined and illustrated. Eleven validliving species are confirmed from the Brazilian littoral and their synonymies and geographic distributions are updated.Redescriptions are provided for Mactrellona alata (Spengler, 1802); Mactrotoma fragilis (Gmelin, 1791); Mulinia clery-ana (d´Orbigny, 1846) and Anatina anatina (Spengler, 1802). The revision of Trinitasia iheringi (Dall, 1897) new combination, reveals the presence of a Tertiary genus among the Recent fauna of South America.


Phytotaxa ◽  
2017 ◽  
Vol 327 (1) ◽  
pp. 57 ◽  
Author(s):  
MICHAEL KESSLER ◽  
ALAN R. SMITH

We introduce the concept of a prodromus for a flora to the ferns and lycophytes of Bolivia, describe the natural setting of Bolivia (topography, climate, vegetation), briefly review the history of pteridological knowledge in the country, present a taxonomic synopsis as well as a key to the fern and lycophyte families of Bolivia, and provide a list of all fern and lycophyte names with Bolivian type material. A new combination is proposed for Polyphlebium herzogii (Rosenst.) A.R.Sm. & Kessler.


Zootaxa ◽  
2017 ◽  
Vol 4272 (4) ◽  
pp. 551
Author(s):  
ROY A. NORTON ◽  
SERGEY G. ERMILOV

Based on the study of type material, other historical specimens, and new collections, the adult of the thelytokous oribatid mite Oribata curva Ewing, 1907 (Galumnidae) is redescribed and the name is recombined to Trichogalumna curva (Ewing, 1907) comb. nov. A confusing history of synonymies and misidentifications is traced in detail, and their effect on published statements about biogeography is assessed. Reliable records of T. curva are only those from North America. The tropical mite Pergalumna ventralis (Willmann, 1932) is not a subspecies of T. curva. The widely-reported Trichogalumna nipponica (Aoki, 1966) and other similar species form a complex with T. curva that needs further morphological and molecular assessment. 


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.


Phytotaxa ◽  
2016 ◽  
Vol 266 (1) ◽  
pp. 27 ◽  
Author(s):  
ANTHONY R. MAGEE ◽  
ODETTE E. CURTIS ◽  
B-E. VAN WYK

Extensive field surveys of the Critically Endangered Central and Eastern Rûens Shale Renosterveld have uncovered that Notobubon striatum, as currently circumscribed, comprises two distinct species. Upon careful examination of the type material it has become clear that names exist for both species. The type specimen of N. striatum clearly matches the lesser known species, a large shrub, ca. 1 m. tall, with a powerful anise-scent and which is restricted to the banks of seasonal rivers and watercourses in the Central and Eastern Rûens Shale Renosterveld. The second and better known entity, with a wider distribution, corresponds to the type material of Dregea collina Ecklon & Zeyher. As such, a new combination, Notobubon collinum (Ecklon & Zeyher) Magee, is here made to accommodate this taxon, restricted to dry quartz and silcrete patches or outcrops in Eastern Rûens Shale Renosterveld. In their revised circumscriptions N. striatum and N. collinum are readily distinguished by habit, scent, leaf size and division, as well as leaf lobe shape and sepal size. Comprehensive descriptions of both species are provided, together with notes on their ecology and conservation status, and the existing key to the species of Notobubon updated. This brings the number of recognised species in the genus to thirteen.


Zootaxa ◽  
2018 ◽  
Vol 4449 (1) ◽  
pp. 1 ◽  
Author(s):  
MARIANA CHANI-POSSE ◽  
ALFRED F. NEWTON ◽  
ASLAK KAPPEL HANSEN ◽  
ALEXEY SOLODOVNIKOV

A checklist of all described species of Philonthina, a subtribe of the staphylinid tribe Staphylinini, known to occur in Central and South America (CASA) is presented. Included for each species, and for synonyms known from CASA, is a reference to the original description, type locality and type depository, and for each species the known distribution within and outside CASA. Type material was sought in the main European and American collections where it is deposited (BMNH, MNHUB, IRSNB and FMNH) and is summarized for all indigenous CASA species, with lectotypes designated for 16 names and confirmation of holotypes and prior designation of lectotypes when necessary. Based on recent phylogenetic work in Philonthina and our revision of types of CASA species of Philonthus Stephens, 1829 and Belonuchus Nordmann, 1837, some taxonomic changes are proposed. Thirty-one species of Philonthus are transferred to Belonuchus (16), Gabrius Stephens 1829 (14), and Bisnius Stephens 1829 (one) resulting in the following new combinations: B. abnormalis (Sharp 1885), B. celatus (Sharp 1885), B. corticalis (Sharp 1885), B. extremus (Sharp 1885), B. infimus (Sharp 1885), B. iteratus (Sharp 1887), B. latecinctus (Sharp 1885), B. lucilius (Sharp 1885), B. muticus (Sharp 1876), B. optatus (Sharp 1885), B. platypterus (Sharp 1885), B. rufiventris (Sharp 1887), B. rufocaudus (Sharp 1885), B. rufopygus (Sharp 1885), B. serraticornis (Sharp 1876), B. supernus (Herman 2001), G. approximans (Sharp 1885), G. armatipes (Sharp 1885), G. atricolor (Sharp 1885), G. championi (Sharp 1885), G. dampfi (Bernhauer 1929), G. elegans (Sharp 1885), G. forsterianus (Scheerpeltz 1960), G. misellus (Sharp 1885), G. nugax (Sharp 1885), G. ovaticeps (Sharp 1885), G. peruvianus (Bernhauer 1916), G. planulatus (Sharp 1885), G. rusticus (Sharp 1885), G. serpens (Sharp 1885) and Bi. subaeneipennis (Bernhauer 1916). Endeius nitidipennis Solier 1849 is transferred to Gabrius, resulting in the following new combination, G. nitidipennis (Solier 1849). Leptopeltus carchiensis Chani-Posse & Asenjo 2013 is proposed as junior synonym of Philonthus divisus Sharp 1891, which is transferred to Leptopeltus Bernhauer 1906 resulting in a new combination: Leptopeltus divisus (Sharp 1891). Belonuchus penetrans Silvestri 1946 is transferred to Pridonius Blackwelder 1952 as a new combination. Lectotypes are designated for Atopocentrum mirabile Bernhauer 1906, Philonthus armatipes Sharp 1885, Ph. atricolor Sharp 1885, Ph. championi Sharp 1885, Ph. misellus Sharp 1885, Ph. planulatus Sharp 1885, Ph. rusticus Sharp 1885, Ph. serpens Sharp 1885, Ph. abnormalis Sharp 1885, Ph. celatus Sharp 1885, Ph. infimus Sharp 1885, Ph. latecinctus Sharp 1885, Ph. muticus Sharp 1876, Ph. platypterus Sharp 1885, Ph. rufocaudus Sharp 1885 and Ph. rufopygus Sharp 1885. Of the 543 currently known species of Philonthina reported from CASA, at least 14 are believed to be adventive from elsewhere, 56 may occur naturally elsewhere, and 473 (87%) are evidently endemic to this region. Of the 31 genera represented by these described species, 20 (65%) are endemic to CASA. One genus, Gabronthus Tottenham 1955, is adventive. However, the actual philonthine fauna of CASA will undoubtedly be much larger, and the generic composition highly modified, when the fauna is fully explored and studied within a phylogenetical framework. 


Zootaxa ◽  
2011 ◽  
Vol 2735 (1) ◽  
pp. 28 ◽  
Author(s):  
KNUT ROGNES

The type material of the nominal species Caiusa coomani Séguy, 1948 (Diptera, Calliphoridae), now placed in Phumosia Robineau-Desvoidy, 1830, has been examined and a lectotype designated to fix the interpretation of the name. In Hong Kong the larval stages of the species is a predator on the egg masses in foam nests of the brown tree frog Polypedates megacephalus Hallowell, 1861 (Anura, Rhacophoridae). Phumosia coomani is known from China, Japan and Vietnam. Discrepancies between the figured genitalia and the external features in Chinese reference works are pointed out.


2016 ◽  
Vol 56 (2) ◽  
pp. 115-119 ◽  
Author(s):  
Zbyněk Šimůnek ◽  
Christopher J. Cleal

Abstract A study of Ettingshausen’s type material of Neuropteris coriacea stored in the Geologisches Bundesanstalt in Vienna has demonstrated that they are conspecific with Havlenaea praeovata (Němejc) Šimůnek & Cleal (Carboniferous medullosalean pteridosperm). Because of priority, the epithet coriacea must take precedence, and a new combination is proposed: Havlenaea coriacea (Ettingshausen) Šimůnek & Cleal, comb. nov.


1978 ◽  
Vol 9 (1) ◽  
pp. 47-62 ◽  
Author(s):  
Göran Nordlander

AbstractThe type material of most European nominal species previously placed in Rhoptromeris and of some other species is studied. Notes are given on the type material, 10 lectotypes are designated and the identity of the species is discussed. Three valid Rhoptromeris species are found: R. heptoma (Hartig) [type species], R. villosa (Hartig) and R. rufiventris (Giraud) n.comb. The latter is the type species of Hexamerocera Kieffer which is synonymized with Rhoptromeris. The genus Rhoptromeris is described and compared with related genera. The three species found to be valid are figured and redescribed, and also a new species, R. nigriventris, is described from Sweden. R. heptoma is an important parasitoid of Oscinella frit (L.) (Dipt.: Chloropidae).


2013 ◽  
Vol 145 (6) ◽  
pp. 603-625 ◽  
Author(s):  
Mar Ferrer-Suay ◽  
Jesús Selfa ◽  
Juli Pujade-Villar

AbstractAlloxysta Förster, 1869 (Hymenoptera: Figitidae) type material of 19 nominal species deposited in the Canadian National Collection of Insects (Ottawa, Ontario, Canada) and the United States National Museum of Natural History (Washington, District of Columbia, United States of America) were studied. Nine species are treated as valid: A. australiae (Ashmead, 1900), A. commensuratus Andrews, 1978, A. japonicus (Ashmead, 1904), A. lachni (Ashmead, 1885), A. longiventris Baker, 1896, A. minuscula Andrews, 1978, A. nothofagi Andrews, 1976, A. vandenboschi Andrews, 1978, and A. xanthopsis (Ashmead, 1896). The following synonymies are established: A. affinis (Baker, 1896) and A. quebeci Andrews, 1978 junior synonyms of A. castanea (Hartig, 1841); A. alaskensis Ashmead, 1902 and A. coniferensis Andrews, 1978 junior synonyms of A. macrophadna (Hartig, 1841); A. bicolor (Baker, 1896) and A. anthracina Andrews, 1978 junior synonyms of A. obscurata (Hartig, 1840); A. dicksoni Andrews, 1978 junior synonym of A. pilipennis (Hartig, 1840); and A. leguminosa (Weld, 1920), A. megourae (Ashmead, 1887), and A. rauchi Andrews, 1978 junior synonyms of A. brevis (Thomson, 1862). The type material of A. schlingeri Andrews, 1978 and A. halli Andrews, 1978 could not be found and we consider them as nomina dubia. Alloxysta vandenboschi Andrews is removed from synonymy with A. obscurata and considered a valid species. Comments on the type material are given. Complete redescriptions and images are presented for the valid species.


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