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ZooKeys 29: 49–71 (2009)
A revision of the genus Zyras (Zyras) Stephens, 1835. I. Current classification status and...
doi: 10.3897/zookeys.29.218
RESEARCH ARTICLE
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A revision of the genus Zyras (Zyras) Stephens, 1835
(Coleoptera, Staphylinidae, Aleocharinae).
I. Current classification status and
the redefinition of the genus
Peter Hlaváč1, Tomáš Jászay2
1 Na doline 14, SK-040 14 Košice, Slovakia 2 Museum of Šariš, Natural History Department, Radničné nám.
13, SK-085 01 Bardejov, Slovakia
Corresponding author: Peter Hlaváč (phlavac@stonline.sk)
Academic editor: Jan Klimaszewski | Received 25 October 2009 | Accepted 10 November 2009 | Published 11 December 2009
Citation: Hlaváč P, Jászay T (2009) A revision of the genus Zyras (Zyras) Stephens, 1835 (Coleoptera, Staphylinidae,
Aleocharinae). I. Current classification status and the redefinition of the genus. Zookeys 29: 49–71. doi: 10.3897/
zookeys.29.218
Abstract
The genus Zyras is redefined and redescribed based on the study of the type species Zyras haworthi
(Stephens). Illustrations of all important morphological characters are provided. The status of the genus
Zyras (s.l.) is discussed. A list of all species attributed to the subgenus Z. (Zyras), including the species
described as Zyras (s.str.), is also given.
Keywords
Coleoptera, Staphylinidae, Aleocharinae, Lomechusini, Zyras, taxonomy, myrmecophily
Introduction
The Lomechusine genus Zyras Stephens, with currently 802 species and 54 subgenera
(Hlaváč, Newton and Maruyama, in prep.), is certainly one of the largest and most
problematic genera of the subfamily Aleocharinae. All species of the genus are believed
to be free predators (synechtrans) of various species of ants. The taxonomic chaos in
this genus is manifested by the fact that 122 species were described only as Zyras without any affilation to a subgenus. Another 68 species originaly described as Zyras were
subsequently synonymyzed or transferred to different genera.
Copyright P. Hlaváč, T. Jászay. This is an open access article distributed under the terms of the Creative Commons Attribution License, which
permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Peter Hlaváč & Tomáš Jászay / ZooKeys 29: 49–71 (2009)
Until 2006, seven subgenera already have been raised to generic level, Myrmoecia (Mulsant & Rey) by Seevers (1978), Aulacocephalonia (Bernhauer) and Homalodonia (Bernhauer) by Kistner and Jacobson (1981), Paramyrmoecia (Scheerpeltz) by
Kistner and Elliot (1985), Macrogerodonia (Bernhauer) and Stichodonia (Bernhauer)
by Pace (1986a, 1999b) and Trachydonia (Bernhauer) by Kistner (1997). Maruyama
(2006) revised the complex of subgenera Pella Stephens, Lepla Tottenham, Pellochromonia Reitter and Myrmelia Mulsant & Rey, in which he synonymyzed all these taxa
with Pella and Pella was treated as a valid genus. Finally, Assing (2009) raised Peltodonia (Bernhauer) to the genus level. The genus Razia Blackwelder, 1952 (new name for
Allocota Bernhauer, 1916; not to be confused with Aloconota Thomson, 1958) is now
placed in the tribe Homalotini and it is a valid subgenus of Gyrophaena Mannerheim,
1830 (Newton and Thayer 2003).
As a consequence of these changes, the following 52 subgenera of the genus Zyras
have remained valid (Hlaváč, Newton and Maruyama, in prep.): Acanthocnemidonia
Bernhauer, Acrothoraconia Bernhauer, Androdonia Bernhauer, Anophthalmodonia Bernhauer, Antronia Bernhauer, Aplastonia Bernhauer, Apostenonia Bernhauer, Apterygodonia Scheerpeltz, Aulacodonia Bernhauer, Botsa Blackwelder, Callodonia Bernhauer, Cameronodonia Dvořák, Camonia Bernhauer, Cephalodonia Bernhauer, Colpodonia Bernhauer, Craspa Blackwelder, Crateodonia Bernhauer, Ctenodonia Wasmann, Dentothalmonia Last, Diaulaconia Bernhauer, Euryalonia Bernhauer, Eurydonia Bernhauer, Euryncephalodonia Scheerpeltz, Euryndonia Bernhauer, Fealina Bernhauer, Glossacantha
Gemminger & Harold, Grammodonia Bernhauer, Hylozyras Iablokoff-Khnzorian, Isothoracodonia Bernhauer, Lastia Dvořák, Leptodonia Bernhauer, Neotropopella Scheerpeltz, Pachydonia Bernhauer, Paragrammodonia Bernhauer, Parophthalmonia Bernhauer, Platydonia Bernhauer, Polydonia Bernhauer, Pycnodonia Bernhauer, Remionia
Blackwelder, Rhopalodonia Cameron, Rocnema Blackwelder, Sinozyras Pace, Subversoris
Last, Synthoracodonia Scheerpeltz, Taprodonia Cameron, Termidonia Motschulsky, Termitelia Cameron, Termitodonia Cameron, Trigonodonia Bernhauer, Trigonozyras Cameron, Tropidonia Bernhauer, Visendor Last.
The logical question must be “Is it really possible that all these very numerous taxa,
distributed worldwide, form a monophyletic group?” This question is not new and it
has already been raised twice, first by Seevers (1965: 238) [“The taxonomic state of the
vast Zyras complex is one of great confusion and the proposal of more than 50 subgenera has
not helped clarify matters very much”] and later by Kistner (1972: 148) [“Also each species
alleged to Zyras (s. str.) in the literature will need to be checked before its inclusion in the
redefined genus is settled. For example, I have not seen a species from sub-Saharan Africa
which really belongs to this genus. It is highly likely that Zyras in the future will be a very
small genus”]. We fully agree with these two opinions, except for the number of species
of true Zyras, which is anticipated to grow to at least 200 species.
The distribution of the genus seems to be mainly in the holarctic region with only
three species in the USA and Canada (Klimaszewski et al. 2005), five species in the
western Palaearctic region and a large number of species in eastern Palaearctic, Oriental and perhaps also in the Australian regions. We have not seen, like Kistner (1972),
A revision of the genus Zyras (Zyras) Stephens, 1835. I. Current classification status and...
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any true Zyras from sub-Saharan Africa or from America south of USA. Of six species
of Zyras reported by Ashe (Navarrete-Heredia et al. 2002) from Mexico, two species
already have been transferred to another genus, Pella fauveli (Sharp) and Myrmoecia
tapinomatis Mann (Klimaszewski et al. 2005). The remaining four species should be
checked, but they, highly likely, will not be members of true Zyras either.
We are sure that many, if not all, species currently attributed to different subgenera
of Zyras, have nothing or very little in common with the true Zyras. For the subgenera
Diaulaconia (Hlaváč 2005: 153) and Glossacantha (Hlaváč 2005; Maruyama 2006,
respectivelly) that has been already discussed, although the new status of both genera
has not been officially changed. In our opinion, Zyras is a very characteristic and well
defined genus, and any further fragmentation should be carefully re-considered.
The majority of subgenera, still attributed to Zyras, were very poorly defined mainly by Bernhauer [34 subgenera described in the period of 1928–1936, four were later
renamed by Blackwelder (1952) and one is synonym], Cameron [six subgenera, one
renamed later by Dvořák (1981)], Scheerpeltz (four subgenera in 1963–1976), Last
[4 subgenera, one later renamed by Dvořák (1984)] and Wasmann (3 subgenera, one
synonym) (Hlaváč, Newton and Maruyama, in prep.). Unfortunately even the final
and most recent papers by Pace (1999a, 1999c) did not bring any light to the Zyras
taxonomic problem.
Material and methods
The main goal of this article is to redefine the genus Zyras based on its type-species,
Zyras haworthi (Stephens). The material used for this study was taken from some institutions listed below.
Specimens prepared for the morphological study were examined with Leica S8APO stereo-microscope and Nikon SMZ – 1B stereo-microscope with diffuse lighting
at magnifications up to 105×. Male genitalia and other dissected parts were studied
using a Meopta transmitted-light microscope at magnification up to 450×. Genital
segments were dissected and treated with lactic acid. All drawings were made using
a drawing tube. The dissected and mounted parts were mounted and pinned with
the specimen.
Depository abbrevations
The material is deposited in following collections:
CMS
CPH
CVA
NMW
SDEI
SMB
Collection of Michael Schülke, Berlin, Germany;
Collection of Peter Hlaváč, Košice, Slovakia;
Collection of Volker Assing, Hannover, Germany;
Naturhistorisches Museum (Harald Schilhammer), Vienna, Austria;
Senckenberg Deutsches Entomologisches Institut (Lothar Zerche), Germany;
Šarišské Múzeum Bardejov (Tomáš Jászay), Slovakia.
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Tribe Lomechusini Fleming, 1821
Genus Zyras Stephens, 1835
Zyras Stephens, 1835: 430. Type species: Zyras haworthi (Stephens), established by
decision of the International Commission on Zoological Nomenclature (ICZN
1961, Opinion 599)
Zyras Stephens: Cameron, 1939: 497 (key to subgenera and species of India, Myanmar
and Sri Lanka); Kistner 1972: 143 (redescription); Scheerpeltz 1974: 39 (key to
African subgenera); Seevers 1978: 153 (key to Nearctic species); Dvořák 1980 (key
to species of Czech and Slovak Republic, including Pella, Lepla, Pellochromonia,
Zyras, Myrmoecia); Dvořák 1984: 200 (key to Palaearctic species including China);
Hastir and Gaspar 2001 (biology); Klimaszewski et al. 2005: 714 (restricted redefinition, key to species of America north of Mexico).
Diagnosis. Zyras (Zyras) can be distinguished from the other genera of Lomechusini by a
combination of the following characters: 1) whole body shiny, unicoloured or often with
different colouration for head, pronotum, elytra and abdomen, sometimes covered with
long setae; 2) all antennomeres petiolate, antennomere III about as long as pedicel; 3)
neck absent; 4) pronotum usually with well-defined median antebasal fovea; 5) abdomen
simple, not physogastric, parallel-sided; 6) simplified aedeagus, median lobe with enlarged
basal capsule and narrowly conical apical lobe; 7) spermatheca sclerotized, very small with
narrowly elongate capsule and with extremely long and highly coiled spermathecal duct.
Description. Body (Fig. 1) slender, subparallel-sided. Body length highly variable,
ranging from 3–9 mm, whole body always shiny, unicoloured, or often with different
colouration for head, pronotum, elytra and abdomen.
Head (Figs 2, 3) slightly wider than long, posterior margin slightly covered by anterior edge of pronotum, neck absent; temples long, round, about as long as diameter
of eyes or longer; occipital suture present, not visible dorsally, ventrally reaching hypostoma, hypostoma narrow; surface with erect or appressed setae. Gula long, evenly
divergent from anterior to posterior; submentum fused to gula, broadly expanded anteriorly. Eyes large, oval in lateral view, prominent.
Antennae (Fig. 4) with all antennomeres petiolate, antennomere III about as long
as II, when bent backwards slightly exceeding base of pronotum.
Labrum (Fig. 5) much wider than long, with shallow median excavation; surface
covered with numerous pseudopores and about ten real pores, except on posterior and
lateral areas; antero-lateral areas each with 4–6 macrosetae of different length.
Mandibles (Figs 6–9) almost symmetrical, lacking teeth, with 3–4 small setae
present dorsally, mesal areas of dorsal and ventral surfaces covered with numerous
pseudopores, prostheca with inner margin pubescent.
Maxilla (Fig. 10) is generalized in shape like for other Lomechusini, with elongate galea
and shortened lacinia, palpomere I minuscule, palpomere II slightly curved and gently shorter that palpomere III, terminal palpomere about three times as short as III, pointed apically.
A revision of the genus Zyras (Zyras) Stephens, 1835. I. Current classification status and...
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Figure 1. Zyras (Zyras) haworthi (Stephens), dorsal view (approximative length of photograped specimen is 7.1 mm)
Mentum (Fig. 11) trapeziform, posterior and anterior margins truncate, with setae,
surface covered with pseudopores bearing minute setae, and about 6–8 pores with
longer setae present on antero-lateral areas.
Labium (Fig. 12) with prementum with two real pores and one setal pore mesolaterally, with about 30–40 pseudopores behind medial setae, apodeme with large,
truncate process, lateral lobes of apodeme gently curved, assimetrical, bifurcate apicaly.
Ligula bilobed, each lobe long, pointed apically, with fine apical seta. Labial palpus
with first segment long, more than twice as long as second and clearly thicker, third
segment slightly longer than second and about twice as slender as second.
Pronotum slightly wider than long (Fig. 1), anterior margin straight, posterior margin evenly rounded, posterior corners small but well-defined, smooth or entirely or
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2
3
Figures 2–3. Zyras (Zyras) haworthi (Stephens). 2 head, dorsal aspect 3 head, ventral aspect (scale = 0.5mm)
4
5
Figures 4–5. Zyras (Zyras) haworthi (Stephens). 4 antennae (scale = 0.5mm) 5 labrum, dorsal (scale = 0.1mm)
partially coarsely punctured and sparsely covered with erect long setae, macrosetae on
lateral margins present, well-defined, median antebasal fovea usually present (may be
missing in some species, for instance Z. bakerianus).
Elytra subparallel-sided (Fig. 1) with well-defined sutural groove throughout, combined width of elytra about twice as wide as long on suture, sutural striae well-defined
through whole length. Scutellum triangular.
Mesoventrite (Figs 13, 14) much shorter than metaventrite, coarsely and densely punctured, setation only on sides, mesoventral process large, round. Mesocoxal cavities sepa-
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7
8
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9
Figures 6–9. Zyras (Zyras) haworthi (Stephens). 6 left mandible, dorsal aspect (scale = 0.1mm) 7 rigth
mandible, dorsal aspect (scale = 0.1mm) 8 rigth mandible, ventral aspect (scale = 0.1mm) 9 left mandible,
ventral aspect (scale = 0.1mm)
rated, isthmus wide but short. Metaventrite rectangular, slightly wider than long, shining,
irregularly and coarsely punctured, with long erect setae, metaventral process truncate.
Legs (Kistner, 1972: 145, Fig. 3, B, C, D) with procoxae very long, only slightly
shorter than profemur, mesocoxae suboval, metacoxae subtriangular; pro- and mesotrochanter small, metatrochanter slightly larger, rounded at apex; femora flattened,
narrowest at base, with punctures and setation; all tibiae straight, very slightly dilated
apicad, with dense setation, each apex with two stout setae; tarsal formula 4-5-5, tarsi
generalised, metatarsus twice as long as protarsus.
Abdomen simple, not physogastric, parallel-sided, at base with punctures and with
long setae on side; paratergites well-developed on tergites III–VII; tergites with posterior margin straight; sternite with surface moderately to densely covered with setae;
eighth abdominal segment (Figs 15–18) species characteristic and also bearing sexual
characters; tergite VIII (Figs 15, 17) narrowed posteriad, truncate apically, apex crenate
or dentate, sternite VIII (Figs 16, 18) narrowed posteriad, at apex rounded in male
and truncate in female, apical setae in female longer and thicker than in male. Ninth
tergite as in (Figs 19, 20), lateral lobes in male asymmetric, absent in female as in most
Aleocharines (Maruyama 2006). Ninth sternite of male as in (Figs 21, 22) elongate,
somewhat pointed at base, expanded apicad and truncate at apex, with well-defined
sharp corners, oblong in middle, bearing setae which are longer and dense on sides.
Aedeagus (Figs 23–25) simple, median lobe composed of enlarged basal capsule and
narrowly conical apical lobe, copulatory piece weakly-defined or absent. Parameres (Fig. 26)
long, clearly longer than apical lobe, composed of condylite, paramerite and velum, apical
lobe of paramerite bears four macrosetae, apical lobe elongate, exceeding apex of velum.
Spermatheca (Fig. 26) sclerotized, very small with narrowly elongate capsule, capsule curved and slender apicad, with extremely long spermathecal duct, coiled many
times forming a bundle.
Biology. In general, it is believed that all species of Zyras (Zyras) are free living
predators or synechtrans of different species of ants according to Wasmann’s categori-
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10
12
11
Figures 10–12. Zyras (Zyras) haworthi (Stephens). 12 maxilla (scale = 0.1mm) 11 mentum (scale =
0.1mm) 12 labium (scale = 0.1mm)
13
14
Figures 13–14. Zyras (Zyras) haworthi (Stephens). 13 metaventrite and mesoventrite lateral (scale =
1mm) 14 metaventrite and mesoventrite ventral (scale = 1mm)
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17
16
18
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Figures 15–18. Zyras (Zyras) haworthi (Stephens). 15 tergite VIII male 16 sternite VIII male 17 tergite
VIII female 18 sternite VIII female (scale = 0.5 mm)
19
20
Figures 19–20. Zyras (Zyras) haworthi (Stephens). 19 tergites IX and X male (scale = 0.5 mm) 20
tergites IX and X female (scale = 0.5 mm)
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Peter Hlaváč & Tomáš Jászay / ZooKeys 29: 49–71 (2009)
21
22
Figures 21–22. Zyras (Zyras) haworthi (Stephens). 21 sternite IX male (scale = 0.5 mm) 22 apex of
sternite IX male (scale = 0.1mm)
23
24
Figures 23–24.Zyras (Zyras) haworthi (Stephens). 23 aedeagus, ventral aspect 24 aedeagus, lateral aspect (scale = 0.5mm)
A revision of the genus Zyras (Zyras) Stephens, 1835. I. Current classification status and...
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26
Figures 25–26. Zyras (Zyras) haworthi (Stephens). 25 paramera (scale = 0.5mm) 26 spermateca (scale
= 0.5mm)
zation (Hölldobler and Wilson, 1990). However there is almost no clear evidence for
this. Hastir and Gaspar (2001) showed that it is difficult to classify Zyras haworthi in
any of Wasmann’s categories. They have also shown that Zyras haworthi is more numerous in localities where Formica sanguinea Latreille is also present.
Distribution. Actually worldwide distributed, but most probably restricted to the Palearctic, Nearctic, Oriental and Australian regions (see discussion above, Introduction). However, due to current taxonomic problems of the genus, it is not possible to be more precise.
Zyras (Zyras) haworthi (Stephens)
Figures 1–26
Aleochara haworthi Stephens, 1832: 126. Type locality: Norfolk
Bolitochara elegans Heer, 1839: 350. Type locality: Helvetia
Zyras nigricollis Motschulsky, 1845: 41. Type locality: Tschougoueff, Russie méridionale
Material examined. Austria: 1 ♀: Austria, Mistelbach env., Eichenwald, 11.V.2002/M.
Schülke (CMS); 1 ♂: Bisamberg near Vienna, 25.VII.10, coll. Künnemann (SDEI); 1
♀: Steiermark, coll. Stierlin (SDEI); 1 ♂: Styria, Reitter, coll. Künnemann (SDEI). Azerbaijan: ♂: Kasp.Meer-Geb., Talysch, 1897, von Heyden (SDEI). Bosnia and Hercegovina: 3♂♂: Bjelašnica Plan., Gipfelregion, Bosn., 1902, coll. Leonhard (SDEI); 2♂♂:
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Peter Hlaváč & Tomáš Jászay / ZooKeys 29: 49–71 (2009)
Bosnia, 1902, Maklen-Pass, O. Leonhard (SDEI); 1 ♂: Herzegovina, Jablanica, 1901,
O. Leonhard (SDEI). Bulgaria: 4♂♂, 3♀♀: NO Bulg., Senokos, 20km O Tolbuchin,
4.5.-19.6.1987, leg. Penev, Querc. roboris et pedunculiflorae, Barberfallen (SDEI); 1 ♀:
Bulg., Or. Eminska Planina, Vlas, 10.V.1987, leg. Behne, Heinig, aus Laubschicht gesiebt unter Quercus und Ulmus carpinifolia, (CVA); 2♀♀: Bulg., Samokov, M. Hilf,
1911, Coll. O. Leonhard (SDEI); 1 ♀: NO Bulg., Srebarna, 20km Wsilistra, 17.6.11.7.1987, leg. Penev (SDEI); 1 ♀: Bulg., Rila-Geb., 23.VII.1985, Musala, 2500 m,
leg. Zerche (SDEI). Czech Republic: 3♂♂: Prag, Coll. Kraatz (SDEI); 1♀: Prag, Skalitz[ky], Coll. Weise (SDEI); 1♀: Prag, coll. Stierlin (SDEI); 1♀: Bohemia (SDEI); 1♂,
2♀♀: Prag, (Dieck), coll. von Heyden (SDEI); 2♀♀: Prag, Lokay, coll. von Heyden
(SDEI); 1♂: Moravia, Coll. Koltze (SDEI); 3♂♂, 2♀♀: Prag, Coll. Koltze (SDEI); ♂:
Slatz, Prag, Stussiner, Coll. Weise (SDEI); 1ex.: Paskau [= Paskov], V-95, coll. Koltze
(SDEI). Croatia: 3ex.: Oestr [=Oesterreiches] Küstenland, Fužine, 1906, leg. M. Hilf,
Coll. O. Leonhard (SDEI). France: 1♂: France, Alpes Maritimes, Col de Castillon,
Südseite 350 m nördl. Monti, I. Wolf leg., 5.5.1996 (CMS); 1ex.(lacking last segments
of abdomen): France, Midi Pyréneés, S/Ax les Thermes, Umg. L´Hospitalet, Ariege,
1300m, 21.VI.1999, leg. I. Wolf (CVA); 1♀: Francia, A. Marittime, Sospel, 1.VI.1999,
500m, leg. F. Angelini (CVA); 1♂: Corsica, 1905, Cervione, Coll. O. Leonhard, 21.7.
(SDEI); 1♂, 1♀: Rhone, Cl. Rey, Coll. Leonhard (SDEI). Germany: 1♀: D-Niedersachsen, E Schladen, Hedeper, Westerberg, VI.2001, L. Schmidt (CVA); 1♀: D. Niedersachsen, Hildesheim-Ochter-Trillkegut, 10.VII.2001, Sprick (CVA); 1♂, 1♀: D.
Sachsen-Anhalt, Stendal, Badingen, 24.VI.1993, Sprick (CVA); 1♂: Erzgebirge, Stollberg, Uhmann, 4.6.24 (SDEI); 1♂: Mark, Umgb., Oderberg, 29.V.27 (SDEI); 1♂: Erlang [=Erlangen], Coll. Kraatz (SDEI). Italy: 1♂: Italia, Lazio, Colli Albani, Commune
Rocca di Papa, Monte Cava, 600–800m, 9.05.1998, leg. I. Wolf, (CMS); 1♀: CalabriaOrsomarso, Grisolia (CS), 11.IX.1993, 700m, leg. F. Angelini; 1♂, 1♀: Toscana, I.
Elba, Cavo (LI), 15.5.1998, 250m, F. Angelini (CVA); 1♂, 1♀: Calabria, Sta. Eufemia,
lg. Paganetti, coll. Franklin Műller (SDEI). Macedonia: 1♂: Skoplje, Mac., 25.VI.54,
leg. F. Schubert (NMW). Portugal: 1♀: P-Algarve, 52, W Monchique, 554m, Rubus, 37°18'53N, 8°33'55W, 15.IV.2002, Meybohm (CVA); 1♀: P-Algarve, 46, Monchique, above road to Alferce, 591m, 37°19'20N, 8°31'52W, 10.IV.2002, Meybohm
(CVA). Poland: 1♂: Liegnitz [=Legnica], Pfeil, coll. von Heyden (SDEI); 1♀: Schwdnitz [Schweidnitz = Šwidnica], Letzner (SDEI); 1♀: Gerhardt, Liegnitz [= Legnica],
Coll. Rottenberg, (SDEI); 1♂, 1♀: Mühlgast [near Wohlów.], Rottenberg (SDEI). Romania: 1♀: NE Romania, Negulesti, 25km SE Piatra Neamt, 500m, 18.vi.1996, P.
Hlaváč lgt. (CPH); 1♂: Banat 1909, Herkulesbad, leg. M. Hilf, Coll. O. Leonhard
(SDEI); 1♂: Banat 1909, Orsova, leg. M. Hilf, Coll. O. Leonhard, 7.VI. (SDEI). Serbia: 1♂: Serbia, Pirot env. Zvonce, banja Prskalo, 520m presev [sifting], above river,
28.IV.2002, lgt. T. Jászay (SMB). Slovakia: 1♂: Slovakia (Košice), Herľany env., sifting,
1.v.2004, P. Hlaváč lgt. (CPH); 1♂: Slovakia centr., Bacúch, 6.vii.1990, T. Lackner lgt.
(CPH); 1♂: Pieniny-Poľana, zemné pasce [traps], 30.6.1989, leg. Svatoň (SMB); 1♂:
Nová Bošáca, St. hora, 6.5.93, Majzlan lgt. (SMB); 1♂: Slovakia centr., Trenčín env.,
24.6.99, O. Majzlan lgt. (SMB); 1♂: Parkan [= Štúrovo], Coll. Weise (SDEI). Sloveni-
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ja: 1♀: Slo Zalog, 3.6.1996, Zg. Kašelj, B. Drovenik leg (CVA). Spain: 2♀♀: Spanien,
Lugo, Sierra Ancares, 2.8.1984, leg. J. C. Otero (CVA). Turkey: 1♂: TR Mersin (33),
road to Arslanköy, 5km SE Aladağ, 700m, 36°54'45N 34° 31'44E, leg. 10.5.2004 Brachat & Meybohm (CVA); 1♀: TR.-Mersin [51], road to Arslanköy, 5km SE Aladağ,
700m, 36°54'45N, 34° 31'44E, 10.V.2004, C. Besuchet (CVA); 1♀: TR Antakya 10,
400m, E Yeşilkent, 30.IV.2002, 36°57N, 36°15E, Meybohm & Brachat (CVA); 2♂♂:
Ovacik, Tunceli, 1400m, Asm, F. Schubert, 6/76 (NMW).
Description. Body (Fig. 1) 5.5–7.0 mm long. Head and pronotum dark reddishblack, elytra reddish-brown, lateral part of apices of elytra with black spot, legs yellowish-brown, antennae yellowish-brown with antennomeres I–III lighter.
Head 1.15 times as wide as long, on sides with long erect golden setae. Antennae
(Fig. 4) with scape almost twice as long as pedicel, pedicel slightly longer than antennomere III, antennomeres IV–VII about the same length, IV–VI slightly transverse, antennomeres VII-X rhombic, clearly extended apicad, X shortest, terminal antennomere
about as long as antennomere III, almost twice as long as wide at base, round at apex.
Pronotum (Fig. 1) 1.25 times as wide as long and 1.28 times as long as head, irregularly punctured, setose and with about five long black macrosetae on each side.
Mesoventrite (Fig. 14) regularly, coarsely punctured on the whole surface. Metaventrite 1.5 times as wide as long and 3.5 times as long as mesoventrite (measured in mid
line), smooth in the middle, coarsely punctured on sides, here also with erect golden setae.
Abdomen two-coloured, densely punctured apex of visible tergites III–V dark reddish-brown, base much lighter and bearing setae, tergites VI–VII dark reddish-brown
almost on the whole surface, densely punctured at base and with few but long apical setae, paratergite III–VII well defined covered with setae, paratergites III–V punctured.
Sexual dimorphism: females have different structure of abdominal tergites and
sternites VIII, IX and X (Figs 15–21). Tergite VIII with small median tubercle in male,
tubercle lacking in female, truncate apex is much narrover in male than in female, median excavation deeper in male than in female; sternite VIII round in male, truncate in
female; tergite IX with asymmetric lateral lobes in male, lateral lobes lacking in female.
Host ants. The following ant genera have been reported as hosts of Zyras (Zyras):
Formica sp., Lasius (Dendrolasius) sp., Liometopum sp., Myrmica sp.
Distribution. Almost whole Europe, Armenia, Azerbaijan, Georgia, Russia, Algeria, Tunisia, Japan
Checklist of species of the subgenus Zyras (Zyras) (Stephens)
A detailed world catalogue of the tribe Lomechusini is near completion (Hlaváč, Newton and Maruyama, in. prep.). The purpose of this checklist is to provide a listing of all
species which were described as, or placed subsequently in the subgenus Zyras (Zyras),
or Zyras (s.str.). All species described as Zyras without subgeneric affilation are excluded
from this list. The list is arranged by zoogeographical regions. This division is a practical solution for the better orientation within the genus.
62
Peter Hlaváč & Tomáš Jászay / ZooKeys 29: 49–71 (2009)
Nearctic region:
This area includes America north of Mexico, i.e. USA and Canada. All three species
listed here are true Zyras and were revised recently (Klimaszewski et al. 2005).
1.
2.
3.
obliquus (Casey, 1894: 325) (Myrmedonia). Distribution: USA, Canada
= pseudohaworthi Klimaszewski, 2002: 53
planifer (Casey, 1894: 326) (Myrmedonia). Distribution: USA
= schwarzi Wasmann, 1894: 207 (Myrmedonia)
rudis (LeConte, 1866: 372) (Myrmedonia). Distribution: USA
West Palaearctic region:
This area, as defined here, includes the whole of Europe, northern Africa, Arabian
peninsula, Caspian region and Siberia to Lake Baikal. All five species recorded here are
true Zyras.
4.
5.
6.
7.
8.
collaris (Paykull, 1789: 50) (Staphylinus). Distribution: Europe, Russia (European), Azerbaijan, Georgia, Algeria
cultus Last, 1960: 14. Distribution: Algeria, Eritrea, Angola
fulgidus (Gravenhorst, 1806: 163) (Aleochara). Distribution: Europe, Russia
(European), Georgia, Iran, Near East
haworthi (Stephens, 1832: 126) (Aleochara). Distribution: Europe, Armenia,
Azerbaijan, Georgia, Russia, Algeria, Tunisia, Japan
= elegans (Heer, 1839: 350) (Bolitochara)
= nigricollis Motschulsky, 1845: 41
maculipennis Gridelli, 1921: 87 (Zyras fulgidus var. maculipennis). Distribution:
Caucasus, Kazachstan, Uzbekistan
East Palaearctic region:
This area includes Siberia east from Lake Baikal, Nepal, northern India, China, Taiwan, Koreas, Japan and Russia Far East. Currently there are 36 species described from
this region and one nomen nudum.
9.
10.
11.
12.
13.
abacus Dvořák, 1984: 194. Distribution: Kazakhstan, Kyrgyzstan
beijingensis Pace, 1993: 114. Distribution: China (Beijing)
britannorum Pace, 1992: 140. Distribution: Nepal
chinkiangensis Bernhauer, 1939: 148. Distribution: China (Jiangsu)
coloratus Cameron, 1939: 545 [Zyras (Pella)]. Distribution: India (Uttar Pradesh)
A revision of the genus Zyras (Zyras) Stephens, 1835. I. Current classification status and...
14.
15.
16.
17.
18.
19.
20.
21.
22.
23.
24.
25.
26.
27.
28.
29.
30.
31.
32.
33.
34.
35.
36.
37.
38.
39.
40.
41.
42.
43.
44.
63
condignus Last, 1969: 279. Distribution: India (Uttar Pradesh), Nepal, Vietnam
= distinctus Cameron, 1939: 540, preoccupied, not Zyras distinctus Biering, 1937
cylindricornis Dvořák, 1981: 56. Distribution: Japan, Korea, China (Liaoning)
exasperatus Schubert, 1908: 610. Distribution: India (Himachal Pradesh)
fratrumkadooriorum Pace, 1998: 968. Distribution: China (Hong Kong)
fugax (Sharp, 1888): 289 (Myrmedonia). Distribution: Japan, Korea
gardneri Cameron, 1939: 538. Distribution: India (West Bengal)
hirsutiventris (Champion, 1927: 245) (Myrmedonia). Distribution: India (Uttar Pradesh), Nepal
hauserianus Bernhauer, 1933b: 46. Distribution: China (Xinjiang)
hongkongensis Pace, 1999a: 684. Distribution: China (Hong Kong)
championi Cameron, 1939: 537. Distribution: India (Himachal Pradesh)
illecebrosus Last, 1982: 81. Distribution: Mongolia
iridescens (Sawada, 1970: 49). (Bolitochara) Distribution: Japan
kraatzi Schubert, 1908: 609. Distribution: India (Himachal Pradesh, Uttar Pradesh), Nepal
= ignicauda (Champion, 1927: 245) (Myrmedonia)
manjushri Pace, 1992b: 142. Distribution: Nepal
morvani Pace, 1986b: 182. Distribution: Nepal
nigroaeneus Cameron, 1939: 543. Distribution: India (Himachal Pradesh)
notaticornis Pace, 1998: 971. Distribution: China (Hong Kong, Zheijang)
optatus (Sharp, 1888: 289) (Myrmedonia). Distribution: Japan
pallipes Pace, 1992: 140. Distribution: Nepal
particornis (Sharp, 1888: 290) (Myrmedonia). Distribution: Japan, Russia (Far
East), Korea, China (Liaoning)
perforatus (Champion, 1921: 178) (Myrmedonia). Distribution: India (Sikkim/
West Bengal, Uttar Pradesh), Nepal
pictus (Sharp, 1874: 11) (Ilyobates). Distribution: Japan, Korea
pindarae (Champion, 1921: 179 (Myrmedonia). Distribution: India (Uttar
Pradesh), Nepal
restitutus Pace, 1993: 114. Distribution: China (Sichuan)
ruficauda Cameron, 1939: 543. Distribution: India (West Bengal), Nepal
seminigerrimus Bernhauer, 1933a: 54. Distribution: China (Sichuan)
shaanxiensis Pace, 1998: 971. Distribution: China (Shaanxi)
sibiricus Bernhauer, 1914: 68. Distribution: Russia: Siberia, Korea
song Pace, 1993: 112. Distribution: China (Yunnan)
songanus Pace, 1993: 114. Distribution: China (Beijing)
wei Pace, 1993: 114. Distribution: China (Guizhou)
The occurence of all species of Zyras (Zyras) from Asia is usually restricted to a rather small area, with the exception of Zyras geminus Kraatz, which is widely distrbiuted
as reported in the literature.
64
45.
Peter Hlaváč & Tomáš Jászay / ZooKeys 29: 49–71 (2009)
geminus (Kraatz, 1859: 27) (Myrmedonia). Distribution: Sri Lanka, India, Indonesia (Java, Sumatra), Taiwan , Philippines, Japan (Iriomote Island)
sinorum Rougemont, 2001: 111. Distribution: China (Hong Kong), NOMEN
NUDUM
Indochina:
This region includes southern Myanmar, Thailand, Cambodia, Vietnam and continental Malaysia. There are currently 21 species included.
46.
47.
48.
49.
50.
51.
52.
53.
54.
55.
56.
57.
58.
59.
60.
61.
62.
63.
64.
65.
66.
alboantennatus Pace, 1986a: 460. Distribution: Myanmar
angkoricola Pace, 2004: 292. Distribution: Cambodia, Thailand
bartolozzii Pace, 2003: 68. Distribution: Malaysia (Malay peninsula)
benenensis Pace, 2001: 196. Distribution: Vietnam
birmanus Scheerpeltz, 1965: 350. Distribution: Myanmar
chumphonensis Pace, 2004: 292. Distribution: Thailand
drugmandi Pace, 2004: 293. Distribution: Thailand
ferrugineiventris Scheerpeltz, 1965: 349. Distribution: Myanmar
ferrugineus Cameron, 1939: 541. Distribution: Myanmar
fustigans Pace, 2000a: 77. Distribution: Thailand
glabricollis Scheerpeltz, 1965: 358. Distribution: Myanmar
kambaitiensis Scheerpeltz, 1965: 347. Distribution: Myanmar
malaisei Scheerpeltz, 1965: 345. Distribution: Myanmar
nitens Cameron, 1944: 108. Distribution: Malaysia (Malay peninsula)
pseudobirmanus Scheerpeltz, 1965: 351. Distribution: Myanmar
quasar Dvořák, 1996: 6. Distribution: Vietnam
semiasperatus Scheerpeltz, 1965: 353. Distribution: Myanmar
setosipennis Scheerpeltz, 1965: 356. Distribution: Myanmar
setosivestis Scheerpeltz, 1965: 354. Distribution: Myanmar
thaiorum Pace, 1986a: 460. Distribution: Thailand
variolatus Pace, 2003: 68. Distribution: Malaysia (Malay peninsula)
Asian tropical islands:
This region includes all Indonesia excluding Papua, Malaysia (Borneo: Sabah and
Sarawak) and Philippines. There are 23 species described.
67.
68.
69.
adulescens (Pace, 1987: 212) (Drusilla). Distribution: Malaysia (Borneo: Sabah)
alboterminalis Pace, 2008: 150. Distribution: Malaysia (Borneo: Sabah)
alternans (Cameron, 1925: 45) (Myrmedonia). Distribution: Indonesia (Sumatra)
A revision of the genus Zyras (Zyras) Stephens, 1835. I. Current classification status and...
70.
71.
72.
73.
74.
75.
76.
77.
78.
79.
80.
81.
82.
83.
84.
85.
86.
87.
88.
89.
65
bryanti Cameron, 1943b: 141. Distribution: Malaysia (Borneo: Sarawak)
daiaccorum Pace, 2008: 152. Distribution: Malaysia (Borneo: Sabah)
drescheri Cameron, 1939: 17. Distribution: Indonesia (Java)
elegantulus Cameron, 1939: 20. Distribution: Indonesia (Java)
facundus Last, 1969: 279. Distribution: Indonesia (Java)
= semirufus (Cameron, 1939: 18), preoccupied, not Myrmedonia semirufa Bernhauer, 1902
flavorufus Cameron, 1939: 18. Distribution: Indonesia (Java)
gratellus Cameron, 1939: 20. Distribution: Indonesia (Java)
kinabaluensis Pace, 2008: 148. Distribution: Malaysia (Borneo: Sabah)
louwerensi Cameron, 1939: 19. Distribution: Indonesia (Java)
matangensis Cameron, 1943b: 141. Distribution: Malaysia (Borneo: Sarawak)
montanus (Bernhauer, 1915: 152) (Astilbus). Distribution: Malaysia (Borneo:
Sarawak)
mortuorum Pace, 1990: 99. Distribution: Philippines (Luzon)
nigerrimus Cameron, 1943b: 142. Distribution: Malaysia (Borneo: Sarawak)
paederinus Pace, 2008: 153. Distribution: Malaysia (Borneo: Sabah)
pallipyga Pace, 2008: 150. Distribution: Malaysia (Borneo: Sabah)
preangeranus Cameron, 1939: 17. Distribution: Indonesia (Java)
pervariolosus Pace, 2008: 150. Distribution: Malaysia (Borneo: Sabah)
punctipennis Cameron, 1939: 18. Distribution: Indonesia (Java)
quadriterminalis Pace, 2008: 149. Distribution: Malaysiad (Borneo: Sabah)
shiva Pace, 1987: 216. Distribution: Indonesia (Lombok, Bali)
Southern India and Sri Lanka:
This region includes India south from Himalayan region and Sri Lanka. There are 9
species included.
90.
91.
92.
93.
94.
95.
96.
97.
98.
castaneus (Motschulsky, 1861: 150) (Myrmedonia). Distribution: Sri Lanka
hastatus Fauvel, 1904: 64. Distribution: India (Karnataka)
hirtus (Kraatz, 1859: 25) (Myrmedonia). Distribution: Sri Lanka, Taiwan
indicus Cameron, 1944: 108. Distribution: India (Karnataka)
parageminus Pace, 1988: 335. Distribution: Sri Lanka
rufescens Cameron, 1939: 534. Distribution: Sri Lanka
nilgiriensis Cameron, 1939: 537. Distribution: India (Tamil Nadu)
optimus Cameron, 1939: 534. Distribution: India (Tamil Nadu)
proximus Cameron, 1939: 538. (Zyras (s.str.), TL: Nilgiri Hills) Distribution:
India (Tamil Nadu)
66
Peter Hlaváč & Tomáš Jászay / ZooKeys 29: 49–71 (2009)
Afrotropical region and temperate South Africa:
This region includes sub-Saharan Africa and the Republic of South Africa. All species
attributed today to the true Zyras were described by Horace Last (1956, 1960, 1962,
1977, 1980) and Roberto Pace (1996). We suspect that these African species are not
true Zyras and belong to other subgenera.
99.
100.
101.
102.
103.
104.
105.
106.
107.
108.
109.
basilewskyi Last, 1956: 219. Distribution: Rwanda, Cameroon, Burundi, Ghana, Dem. Rep. Congo
bonus Last, 1977a: 947. Distribution: Dem. Rep. Congo
bramtonus Last, 1962: 222. Distribution: Senegal, Ghana, Dem. Rep. Congo
conjectus Last, 1960: 12. Distribution: Gabon, Spanish Guinea, Angola
flavipennis Last, 1956: 218. Distribution: Burundi, Ghana, Nigeria, Rwanda,
Dem. Rep. Congo
mutarensis Pace, 1996: 231. Distribution: Zimbabwe
nakuruensis Pace, 1996: 231. Distribution: Kenya
nigritus Last, 1980: 176. Distribution: Rep. South Africa (Cape, Natal)
planctos Last, 1977b: 81. Distribution: Ghana
punctus Last, 1967: 109. Distribution: Angola, Burkina Faso, Nigeria, Dem.
Rep. Congo
= punctus var. croceus Last, 1967: 110
tambachensis Pace, 1996: 228. Distribution: Kenya
Australian region:
Australia plus New Zealand, New Guinea and New Caledonia. There are only three
species known from this region.
110. biroi Last, 1980: 161. Distribution: New Guinea
= biroi var. subflavus Last, 1980: 161
111. hirsutus Cameron, 1943a: 353. Distribution: Australia (Victoria)
112. papuanus Pace, 2000b: 159. Distribution: Papua New Guinea
Neotropical region:
Mexico, Central and South America (including Caribbean islands). There are two species from this vast area known today. We believe that true Zyras do not occur in Neotropics and both species probably belong to other genera of Lomechusini.
113. distinctus Bierig, 1937: 281. Distribution: Cuba
114. paecesanus Pace, 1997: 36. Distribution: Colombia
A revision of the genus Zyras (Zyras) Stephens, 1835. I. Current classification status and...
67
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