Literature DB >> 35586542

A generic classification of Xenidae (Strepsiptera) based on the morphology of the female cephalothorax and male cephalotheca with a preliminary checklist of species.

Daniel Benda1,2, Hans Pohl3, Yuta Nakase4, Rolf Beutel3, Jakub Straka1.   

Abstract

The generic taxonomy and host specialization of Xenidae have been understood differently by previous authors. Although the recent generic classification has implied a specialization on the level of host families or subfamilies, the hypothesis that each xenid genus is specialized to a single host genus was also previously postulated. A critical evaluation of the classification of the genera of Xenidae is provided here based on morphology in accordance with results of recent molecular phylogenetic studies. External features of the female cephalothoraces and male cephalothecae were documented in detail with different techniques. Diagnoses and descriptions are presented for all 13 delimited genera. The earliest diverging genera are usually well characterized by unique features, whereas deeply nested genera are usually characterized by combinations of characters. Three new genera are described: Sphecixenos gen. nov., Tuberoxenos gen. nov., and Deltoxenos gen. nov. Five previously described genera are removed from synonymy: Tachytixenos Pierce, 1911, stat. res.; Brasixenos Kogan & Oliveira, 1966, stat. res.; Leionotoxenos Pierce, 1909, stat. res.; Eupathocera Pierce, 1908, stat. res.; and Macroxenos Schultze, 1925, stat. res. One former subgenus is elevated to generic rank: Nipponoxenos Kifune & Maeta, 1975, stat. res. Monobiaphila Pierce, 1909, syn. nov. and Montezumiaphila Brèthes, 1923, syn. nov. are recognized as junior synonyms of Leionotoxenos Pierce, 1909, stat. res. Ophthalmochlus Pierce, 1908, syn. nov., Homilops Pierce, 1908, syn. nov., Sceliphronechthrus Pierce, 1909, syn. nov., and Ophthalmochlus (Isodontiphila) Pierce, 1919, syn. nov. are recognized as junior synonyms of Eupathocera Pierce, 1908, stat. res. A preliminary checklist of 119 described species of Xenidae with information on their hosts and distribution is provided. The following 14 species are recognized as valid and restituted from synonymy: Tachytixenosindicus Pierce, 1911, stat. res.; Brasixenosacinctus Kogan & Oliveira, 1966, stat. res.; Brasixenosaraujoi (Oliveira & Kogan, 1962), stat. res.; Brasixenosbahiensis Kogan & Oliveira, 1966, stat. res.; Brasixenosbrasiliensis Kogan & Oliveira, 1966, stat. res.; Brasixenosfluminensis Kogan & Oliveria, 1966, stat. res.; Brasixenosmyrapetrus Trois, 1988, stat. res.; Brasixenoszikani Kogan & Oliveira, 1966, stat. res.; Leionotoxenoshookeri Pierce, 1909, stat. res.; Leionotoxenosjonesi Pierce, 1909, stat. res.; Leionotoxenoslouisianae Pierce, 1909, stat. res.; Eupathoceraluctuosae Pierce, 1911, stat. res.; Eupathoceralugubris Pierce, 1909, stat. res.; Macroxenospiercei Schultze, 1925, stat. res. New generic combinations are proposed for 51 species: Leionotoxenosarvensidis (Pierce, 1911), comb. nov.; Leionotoxenosbishoppi (Pierce, 1909), comb. nov.; Leionotoxenosforaminati (Pierce, 1911), comb. nov.; Leionotoxenosfundati (Pierce, 1911), comb. nov.; Leionotoxenoshuastecae (Székessy, 1965), comb. nov.; Leionotoxenositatiaiae (Trois, 1984), comb. nov.; Leionotoxenosneomexicanus (Pierce, 1919), comb. nov.; Leionotoxenosprolificum (Teson & Remes Lenicov, 1979), comb. nov.; Leionotoxenosrobertsoni (Pierce, 1911), comb. nov.; Leionotoxenostigridis (Pierce, 1911), comb. nov.; Leionotoxenosvigili (Brèthes, 1923), comb. nov.; Eupathoceraargentina (Brèthes, 1923), comb. nov.; Eupathoceraauripedis (Pierce, 1911), comb. nov.; Eupathocerabucki (Trois, 1984), comb. nov.; Eupathoceraduryi (Pierce, 1909), comb. nov.; Eupathoceraerynnidis (Pierce, 1911), comb. nov.; Eupathocerafasciati (Pierce, 1909), comb. nov.; Eupathocerafuliginosi (Brèthes, 1923), comb. nov.; Eupathocerainclusa (Oliveira & Kogan, 1963), comb. nov.; Eupathocerainsularis (Kifune, 1983), comb. nov.; Eupathoceramendozae (Brèthes, 1923), comb. nov.; Eupathocerapiercei (Brèthes, 1923), comb. nov.; Eupathocerastriati (Brèthes, 1923), comb. nov.; Eupathocerataschenbergi (Brèthes, 1923), comb. nov.; Eupathocerawestwoodii (Templeton, 1841), comb. nov.; Macroxenospapuanus (Székessy, 1956), comb. nov.; Sphecixenosabbotti (Pierce, 1909), comb. nov.; Sphecixenosastrolabensis (Székessy, 1956), comb. nov.; Sphecixenosdorae (Luna de Carvalho, 1956), comb. nov.; Sphecixenoserimae (Székessy, 1956), comb. nov.; Sphecixenosesakii (Hirashima & Kifune, 1962), comb. nov.; Sphecixenosgigas (Pasteels, 1950), comb. nov.; Sphecixenoskurosawai (Kifune, 1984), comb. nov.; Sphecixenoslaetum (Ogloblin, 1926), comb. nov.; Sphecixenosorientalis (Kifune, 1985), comb. nov.; Sphecixenosreticulatus (Luna de Carvalho, 1972), comb. nov.; Sphecixenossimplex (Székessy, 1956), comb. nov.; Sphecixenosvanderiisti (Pasteels, 1952), comb. nov.; Tuberoxenosaltozambeziensis (Luna de Carvalho, 1959), comb. nov.; Tuberoxenossinuatus (Pasteels, 1956), comb. nov.; Tuberoxenossphecidarum (Siebold, 1839), comb. nov.; Tuberoxenosteres (Pasteels, 1950), comb. nov.; Tuberoxenostibetanus (Yang, 1981), comb. nov.; Deltoxenosbequaerti (Luna de Carvalho, 1956), comb. nov.; Deltoxenosbidentatus (Pasteels, 1950), comb. nov.; Deltoxenoshirokoae (Kifune & Yamane, 1992), comb. nov.; Deltoxenosiwatai (Esaki, 1931), comb. nov.; Deltoxenoslusitanicus (Luna de Carvalho, 1960), comb. nov.; Deltoxenosminor (Kifune & Maeta, 1978), comb. nov.; Deltoxenosrueppelli (Kinzelbach, 1971a), comb. nov.; Xenosropalidiae (Kinzelbach, 1975), comb. nov. Xenosminor Kinzelbach, 1971a, syn. nov. is recognized as a junior synonym of X.vesparum Rossi, 1793. Ophthalmochlusduryi Pierce, 1908, nomen nudum and Eupathoceralugubris Pierce, 1908, nomen nudum are recognized as nomina nuda and therefore unavailable in zoological nomenclature. The species diversity of Xenidae probably remains poorly known: the expected number of species is at least twice as high as the number presently described. Daniel Benda, Hans Pohl, Yuta Nakase, Rolf Beutel, Jakub Straka.

Entities:  

Keywords:  Cephalotheca; Strepsiptera; Xenidae; cephalothorax; generic revision; morphology; taxonomy; wasp parasite; wasps

Year:  2022        PMID: 35586542      PMCID: PMC9010403          DOI: 10.3897/zookeys.1093.72339

Source DB:  PubMed          Journal:  Zookeys        ISSN: 1313-2970            Impact factor:   1.492


  23 in total

1.  The unusual visual system of the Strepsiptera: external eye and neuropils.

Authors:  E K Buschbeck; B Ehmer; R R Hoy
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2003-07-19       Impact factor: 1.836

2.  Mating of Xenos vesparum (Rossi) (Strepsiptera, Insecta) revisited.

Authors:  L Beani; F Giusti; D Mercati; P Lupetti; E Paccagnini; S Turillazzi; R Dallai
Journal:  J Morphol       Date:  2005-09       Impact factor: 1.804

3.  Fine structure of adhesive devices of Strepsiptera (Insecta).

Authors:  Hans Pohl; Rolf G Beutel
Journal:  Arthropod Struct Dev       Date:  2004-01       Impact factor: 2.010

4.  The midgut ultrastructure of the endoparasite Xenos vesparum (Rossi) (Insecta, Strepsiptera) during post-embryonic development and stable carbon isotopic analyses of the nutrient uptake.

Authors:  Fabiola Giusti; Luigi Dallai; Laura Beani; Fabio Manfredini; Romano Dallai
Journal:  Arthropod Struct Dev       Date:  2007-01-27       Impact factor: 2.010

Review 5.  Host-parasitoid associations in Strepsiptera.

Authors:  Jeyaraney Kathirithamby
Journal:  Annu Rev Entomol       Date:  2009       Impact factor: 19.686

6.  Frozen Antarctic path for dispersal initiated parallel host-parasite evolution on different continents.

Authors:  Daniel Benda; Yuta Nakase; Jakub Straka
Journal:  Mol Phylogenet Evol       Date:  2019-03-06       Impact factor: 4.286

7.  Total Synthesis, Stereochemical Assignment, and Field-Testing of the Sex Pheromone of the Strepsipteran Xenos peckii.

Authors:  Huimin Zhai; Michael Hrabar; Regine Gries; Gerhard Gries; Robert Britton
Journal:  Chemistry       Date:  2016-03-22       Impact factor: 5.236

8.  Total synthesis, proof of absolute configuration, and biosynthetic origin of stylopsal, the first isolated sex pheromone of strepsiptera.

Authors:  Roman Lagoutte; Petr Šebesta; Pavel Jiroš; Blanka Kalinová; Anna Jirošová; Jakub Straka; Kateřina Černá; Jan Šobotník; Josef Cvačka; Ullrich Jahn
Journal:  Chemistry       Date:  2013-04-29       Impact factor: 5.236

9.  The first molecular phylogeny of Strepsiptera (Insecta) reveals an early burst of molecular evolution correlated with the transition to endoparasitism.

Authors:  Dino P McMahon; Alexander Hayward; Jeyaraney Kathirithamby
Journal:  PLoS One       Date:  2011-06-28       Impact factor: 3.240

10.  A new genus of Strepsiptera, Rozenia gen. n. (Stylopidae), a parasite of bee genera Acamptopoeum and Calliopsis (Andrenidae, Panurginae, Calliopsini).

Authors:  Jakub Straka; Katerina Jůzová; Jan Batelka
Journal:  Zookeys       Date:  2014-09-23       Impact factor: 1.546

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  1 in total

1.  Have female twisted-wing parasites (Insecta: Strepsiptera) evolved tolerance traits as response to traumatic penetration?

Authors:  Kenny Jandausch; Jan Michels; Alexander Kovalev; Stanislav N Gorb; Thomas van de Kamp; Rolf Georg Beutel; Oliver Niehuis; Hans Pohl
Journal:  PeerJ       Date:  2022-08-16       Impact factor: 3.061

  1 in total

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