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Return to
List of CERAMBYCOIDEA of former USSR
11.3.2003
M.L. Danilevsky
(MS Word -> HTML convertation by Andrei Lobanov)
#1
Parandra caspia was recorded for Turkmenia (Kopet-Dag) and for
Transcaspean Iran (Gorgan) - (Araujo-Arigony, 1977) on the base of Lameere
(1902): "habite a Transcaucasie, le nord de la Perse et la Turcomanie."
The records was regarded by A.Semenov (1902) as wrong.
#2
According to Svacha (1987), Callipogon and Ergates belong to
different tribes.
#3
Ergates faber hartigi Demelt, 1952 and E.f.alkani Demelt, 1968 were
regarded by Villiers (1978) as aberrations of females.
#4
According to Vives (2000), Macrotoma Serv.,1832-June is a junitor
homonym of Macrotoma Laporte,1832-April (Diptera). The necessaty of the
name change must be checked in agree with Article 23.9.1. of ICZN (1999).
But even if it must be changed, the necessity of new tribal name
(Prinobiini Vives, 2000) is doubtful. Several other names can be used:
Mallodonitae Thomson, 1860; Stenodontines Lameere, 1902.
According to Vives (2000), Macrotoma germari Dejean, 1835 is a valid
name.
#5
Prinobius is a separate genus, according to Villiers (1978).
#6
According to Sama (1994): Prinobius myardi Muls., 1842 = Prionus
scutellaris Germ., 1817 nec Olivier, 1795 (Pyrodes).
#7
Prinobius s. proksi Slama, 1982 was described from Crete.
#8
In the remark to the original description of Prionus serricollis the
author asked to read the name as serraticollis.
According to Miroshnikov (1998) Rhesus was described by J.Thomson
1860 (nec N.Lesson, 1840) and then replaced to Rhaesus Motschulsky, 1875
(without special remark of replacement).
Rhaesus Motschulsky, 1875 was introduced for Rh. persicus , which is
a synonym of serricollis.
#9
The generic differences between Megopis and Aegosoma is generally
accepted (Villiers, 1978; Sama, 1988). So subgenus Spinimegopis belongs to
Aegosoma.
#10
Meroscelisitae J.Thomson, 1860 (after Monne et Giesbert, 1993).
#11
Bily et Mehl (1989) recorded T. depsarium for Caucasus and Amur
Valley after Horion (1974: 5-6) and Samoilov (1936)
#12
According to the original publication: paradoxus Fald.,1833; not
Fald.,1832, as in Lobanov et al. (1981).
#13
The difference between island and mainland populations of P.insularis
seems to be considerable. P. yakushimanus Ohbayashi, 1964 (Yakushima Is.
and Tanegashima Is.) was regarded as a synonym of P.insularis by Kusama
and Takakuwa (1984), but also as its subspecies (Ohbayashi et al., 1992).
Prionus insularis was recorded for Gornaia Shoria (Altai) by Novikov
and Petuninkin (1987).
#14
Prionus asiaticus was recorded for China Mongolia by Gressitt (1951)
on the base of the description of Prionus henkei Schaufuss, 1879 (=
asiaticus). According to Jakovlev (1887) P. henkei was described "au
gouvernement d'Astrakhan aux environs du mont Bogdo". The records of P.
asiaticus for China or Mongolia is nonsense.
The species was recorded for Elburs (Semenov-Tian-Shanskij, 1927),
but it could concern P. persicus.
#15
According to the original description, Prionus zarudnii.
The species was collected in Karategin Ridge (14km N Novabad, 1700m,
30.7.69 and 5.8.1969, J.Shchetkin leg.) - 2 males and 1 female in the
collection of M.Danilevsky.
#16
A revision of Psilotarsus was published by M.Danilevsky (2000).
#17
Psilopus was traditionally attributed to Motschulsky (1875), but it
was described by Gebler (1859) with a valid species name.
#18
According to personal communication of A.Miroshnikov (1986), several
corrections must be made to the publication of Lobanov et al.(1981,1982):
Prionus semenovianus Plav. 1936 (not 1935)
Xylosteus caucasicola Plav. 1936 (not 1938)
#19
P. (s.l.) semenovianus was transfered to Pogonarthron by Danilevsky
(1999b).
#20
The tribe system of Lepturinae (with Rhamnusiini, Oxymirini,
Enoploderini, Sachalinobiini and so on) is more or less agree with
P.Svacha divisions (1989 in Svacha, Danilevsky, 1989), but Encyclopini is
regarded as separate and of similar evolution level as Xylosteini, as well
as Enoploderini. Several tribes (Rhamnusiini, Oxymirini, Enoploderini)
were named by Danilevsky in "A Check-list :" (Althoff and
Danilevsky,1977). Sachalinobiini was never published.
#21
According to Sama (1993a) Xylosteus caucasicola is a subspecies of X.
spinolae. It was declared that oldest name Psilorhabdium is not valid
because the youngest name Leptorhabdium was chosen by Ganglbauer (1882:
38), as first reviser (Article 24 ICZN).
In the original description: "Leptorhabdium". "Leptorrhabdium" was
introduced by Ganglbauer, 1881 (Best.Tab.)
#22
Xylosteus caucasicola was recorded for European Turkey and Cortodera
umbripennis for Bulgaria (Sama, Rapuzzi, 1999). It is very probable, that
last record was connected with very close Cortodera khatchikovi
Danilevsky, 2001.
#23
Leptorhabdium caucasicum was recorded for Turkey (Torul) by Gfeller
(1972).
#24
The synonymy Encyclops = Microrhabdium was accepted by Lobanov et
al., 1981 (after Gressitt, 1951; inroduced by Gressitt, 1947, Proc.
Entomol. Soc. Washington, 49: 191.).
A lot of other taxonomic and geographical positions were accepted (or
canceled) after different authors or introduced as new (Lobanov et al.,
1981, 1982).
#25
According to (Danilevsky, 1988c):
E. macilentus Kr.= E. parallelus Pic = E. ussuricus Cher.
Grammoptera cyanea = G. plavilstshikovi (Far East Russia and
Sakhalin), later (Danilevsky, 1993) Neoencyclops was regarded as a
subgenus of Grammoptera.
Alosterna chalybeella absent in the mainland
(S.Sakhalin,Kunashir,Japan).
Gaurotina sichotensis stat.n. (= G. superba m. sichotensis) was found
in Khasan district of Far East Russia (1 male in collection of Danilevsky)
and G. superba absent in Russia.
Molorchus starki Shabl., 1936 = M. ussuriensis Plav., 1940 (syn.n.)
Phymatodes vandykei Gress., 1935 = Ph. ussurucus Plav., 1940 (syn.n.)
Xylotrechus salicis Takakuwa et Oda., 1978 = X. nadezhdae Tsher.,1982
(syn.n.)
Tetropium gracilicum was recorded for Shikotan Is. - first record for
Russia, as well as Oligoenoplus rosti (Kunashir) and Chlorophorus diadema
inhirsutus (Kunashir).
Rondibilis (as Eryssamena) schabliovskyi is the only one
representative of the genus in Russian Far East mainland - absent on
islands (possibly it was described before as E. coreana Breuning, 1974).
Eryssamena (or Ostedes) tuberculata absent in Russia. Rondibilis (as
Eryssamena) saperdinus is known from Kunashir, Shikotan and Japan.
Oberea scutellaroides = O. chinensis
#26
Two genera Rhagium and Rhamnusium were separated by E.Vives (2000) in
a small tribe Rhagiini, while other Rhagiini (including Oxymirus) are
grouped in tribe Toxotini.
#27
According to Danilevsky (1992):
Phytoecia pustulata = Ph.pilipennis,
Cortodera transcaspica = persica = lobanovi,
Agapanthia lederi = helianthi
Rhagium caucasicum semicorne st.nov. - first record for USSR (Talysh)
#28
I.K. Zahaikevitch basing on the area analysis supposed (personal
communication), that record of Rhagium inquisitor inquisitor for Crimea
was connected with accident introduction.
#29
B.Namhaidorzh (1972) recorded for Mongolia: Rhagium inquisitor
rugipenne, Gnathacmaeops pratensis, Leptura annularis (as Strangalia
arcuata)
#30
According to Kusama and Takakuwa (1984) the following taxa are absent
in Japan: Rhagium inquisitor rugipennis, Stenocorus amurensis, Brachyta
interrogationis, Acmaeops marginatus, Lepturobosca virens, Gracilia
minuta, Xylotrechus adspersus, Monochamus guttulatus, M.
galloprovincialis, Acanthocinus aedilis, Leiopus albivittis, Eutetraphà
metallescens.
#31
Acalolepta cervina (described from India) absent in Russian fauna. It
was recorded (before the description of A.ussurica) only once (Samoilov,
1936) and absent in Russian materials in all known to me collections.
The presence in Russian mainland fauna another Acalolepta (excepting
A.ussurica) is very doubtful (A. sejuncta is known from Korea).
Samoilov also recorded for Russia: Cylindilla grisescens, Nupserha
alexandrovi (as Oberea, described from China), Phytoecia ferrea (as analis
= mannerheimi). The species was also mentioned for USSR by Plavilstshikov
(1932: 195): "[East Siberia]", missed by Tsherepanov (1985), but recorded
by Krivolutzkaia (in: Tsherepanov, 1996: 139),as Ph. mannerheimi Breun. I
know at least 2 males of Ph. ferrea from Primorie Region in collection of
Zoological Museum of Moscow University (a pair from Mongolie in my
collection).
#32
According to Hayashi (1980: 14) - A.t.bivittis = A.t.ab.nigra Mats.et
Tam.,1940 = A.t.b.ab. plavilstshikovi Podany, 1963. I've checked the
paratypes of A.t.b.ab. plavilstshikovi in Bratislava - it was dark forms
of A.t.bivittis from Tuva.
I've also studied holotype and two paratypes of Rh. minimum Podany in
Frankfurt, so Rhagium inquisitor stshukini = Rh. minimum.
#33
Hesperophanes, Deroplia, Anaesthetis and Exocentrus are attributed by
E.Vives (2000) to Dejean, 1835, as well as Stenocorus to Geoffroy, 1762;
Parmena and Purpuricenus to Dejean, 1821; Opsilia to Mulsant, 1862; Oberea
to Mulsant, 1835; Tetrops to Stephens, 1829.
#34
Tetrops praeusta and T. gilvipes can be definitly distinguished only
with larvae (Danilevsky, Miroshnikov, 1985). A taxon with "gilvipes-like
larvae" is very common in West Europe, but its adults are very similar to
T.praeusta (Svacha, Die Larven der Kafer Mitteleuropas, Band 6)! So
possibly a yellow form of T. gilvipes was described from Europe as T.
praeusta. In that case black beetles from Caucasus are T. praeusta ssp.
gilvipes. And a taxon with "praeusta-like" larvae (sensu Danilevsky and
Miroshnikov, 1985) needs another name.
Any way the stable black colour of Caucasian (and Turkmenian) T.
gilvipes makes impossible its synonymysation with T. praeusta, proposed by
Sama (1988) and accepted by Bense (1995).
But if T. praeusta has "praeusta-like larvae", then European taxon
with "gilvipes-like" larvae (usually yellow, but sometimes black) can be
named T. gilvipes ssp. nigra Kraatz, 1859.
In Russia T. gilvipes seems to be absent, but in Crimea both species
exist, and T. gilvipes often has yellow elytrae, but legs are pale yellow
and elytral pubescence distinctly shorter and less erected.
In West Europe adults of both taxa are (at least usually)
indistinguishable.
Big series of adults from different larvae must be investigated.
#35
According to Hayashi (1980) Eutoxotus caeruleipennis present on
Sakhalin.
#36
According to Danilevsky (1988a) Oberea depressa = O.amurica = O.
transbaicalica.
#37
Stenurella jaegeri was recorded for Crimea (Bakhchisarai) by S.Baidak
(1996b) - first record for Ukraine.
The record of Asias halodendri for Dagestan (2 males,
Rutul,1800m,16.6.94 and 15.7.94) by S.Baidak (1996a) is connected with a
well known population, which represents a new taxon, as well as a
population from Albania (Muraj, 1960).
Paracorymbia tonsa was recorded for Crimea (Bakhchisarai); Pidonia
"lucida" (evidently - lurida), Leiopus femoratus and Stenocorus insitivus
for Poltava Region (Lubny); Ropalopus insubricus for Sevastopol;
Echinocerus bobelayei (as speciosus) for Odessa Region (Primorskoe) by
S.Baidak (1997).
Echinocerus bobelayei (as speciosus) was also recorded for Rostov
Region and Kalmykia (Arzanov et al., 1993; Kasatkin, Arzanov, 1995).
The record of E.bobelayei (as speciosus) for Central Asia by Lobanov
at al. (1982) was made without any comments. The species seems to be
rather common in Kopet-Dag (Turkmenia). One male with the label:
"Turkmenia, Kopet-Dag, Garygala, V.1994, J.Miatleuski leg." is preserved
in my collection.
No species of Plagionotus were recorded for Kopet-Dag by
Plavilstshikov (1940), but this region is included in Plagionotus area in
the map (:429).
L. femoratus was also recorded for Crimea by Zahaikevitch (1991).
#38
Stenocorus vittatus F.-W. = S. suvorovi Rtt. I've studied the types
of S. suvorovi (from Dzharkent) in Budapest. The males really have several
erect setae at elytral base, but no other differences from specimens from
Cenral and North Dzhungaria or from Tarabagatai. I think such character is
not enough for species separation.
#39
Pidonia grisescens described from Urals is according to
Plavilstshikov (1936) E. borealis.
#40
According to Kusama and Takakuwa(1984):
the following taxa are represented in Japan: Nothorhina punctata,
Tetropium fuscum, Acmaeops septentrionis, Stenurella melanura, Nåñydàlis
major, N. morio, N. sachalinensis, Obrium cantharinum, Agapanthia daurica,
Olenecamptus octopustulatus, Oberea inclusa.
the following taxa are represented in Russia by subspecies: Brachyta
b. bifasciata, B. b. japonica, Anoplodera c. cyanea, Leptura d.
duodecimguttata, L. o. ochraceofasciata, Nakanea v. vicaria,
Strangalomorpíà t. tenuis, Necydalis m. major, Necydalis m. aino, Obrium
c. cantharinum, Molorchus m. minor, Cyrtoclytus c. caproides, Asaperda a.
agapanthina, A. r. rufipes, Pseudocalamobius j. japonicus, Egesina b.
bifasciana, Pterolophia j. jugosa, Plectrura m. metallica, Acalolepta l.
luxuriosa, A. s. sejuncta, Mimectatina d. divaricata, Pogonocherus f.
fasciculatus, Eutetraphà ch. chrysochloris, Glenea r. relicta, Oberea i.
inclusa.
Leptura includes several subgenera: Nakanea, Pedostrangalia,
Stenurella, Megaleptura (for L.regalis and L.thoracica).
Paragaurotes suvorovi is a subspecies of P. doris, though usually in
Japan publications: doris = suvorovi.
#41
According to Kusama and Takakuwa (1984) Mesosa japonica is a
subspecies of M. myops.
#42
According to Danilevsky (1998a), Brachyta breiti is represented in
Mongolia.
According to holotype study of B. eurynensis by A.Lobanov (personal
communication of 1987) it is a synonym of B. variabilis. The previously
published (Danilevsky, 1988d) synonymy: B.breiti = B.eurynensis was wrong.
#43
M. sinica was recorded for Far East Russia by Lobanov et al. (1981)
and then by Tsherepanov (1996) without any comments.
According to Hayashi (1979):
Russian parts of the areas of Distenia gracilis and Megopis sinica
must be occupied by nominative subspecies. M. sinica was recorded for
Korea.
Asemum punctulatum is represented in Mongolia (which is rather
doubtful) and in Central Asia (which must be a mistake).
#44
Lee (1982) recorded for Korea: Brachyta amurensis, Pidonia suvorovi,
Grammoptera gracilis, Cornumutila quadrivittata, Judolia cometes, Leptura
regalis, Necydalis pennata, N. sachalinensis, Clytus melaenus,
Pseudocalamobius japonicus, Pterolophia jugosa, Monochamus nitens,
Phytoecia rufipes, Oberea pupillata - the last record must concern
O.heyrovskyi.
#45
According to Podany (1962) Carilia virginea is reperesented in
Siberia by C. v. aemula.
According to Danilevsky (1998a), the traditional name of Siberian
subspecies "thalassina" accepted by Plavilstshikov (1936), Tsherepanopv
(1979), Lobanov et al. (1981), Tsherepanov (1996), can not be used here as
it was introduced for red-thorax aberration from Austria!
Carilia v. aemula Mnnh. = C. sibirica Podany - the type of the former
was investigated in Bratislava by Danilevsky; the synonymy was published
by Tcherepanov (1996).
#46
According to Danilevsky (1998a): C.v. kozhevnikovi is not a separate
species.
#47
According to Mroczkowsky (1986, 1986a, 1987), Opinions: 1473, 1494
(ICZN, 1988a,1988b) were accepted, conserving following names: Tetropium
Kirby, 1837 (= Isarthron Dejean, 1835), Leptura marginata F., 1781 (now
Acmaeops marginatus (not Leptura marginata O.F.Muller in Allioni, 1766).
Sama (1991) published Isarthron = Tetropium, ignoring the
conservation.
#48
I've studied (2001) the holotype male of Acmaeops sachalinensis
(preserved in Zoological Institute in St.-Petersburg) with the label in
Russian: "[Sakhalin, Nikolskiy Bay, Nikolsky leg.]" and another small
lable with dated: 17.4.09. It is a colourless specimen of A.
angusticollis, so A. angusticollis = A. sachalinensis. There is also a
series of similar colourles specimens of G. pratensis with similar labels
in Russian "[Sakhalin, Nikolsky leg.]" in the Museum.
#49
The relation between G.pratensis and G. brachypterus was shown with
larval characters by P.Svaha (Svaha, Danilevsky, 1989).
#50
According to Danilevsky et Miroshnikov (1985):
Cortodera syriaca Pic 1901 was discovered in Nakhichevan Republic.
Purpuricenus caucasicus Pic is a species, distributed in Crimea,
Caucasus and possibly in West Europe (later was regarded as a subspecies
of P. budensis by Sabbadini and Pesarini,1992 from Armenia and Turkey).
Molorchus monticola, is a species distributed in Talysh and Armenia.
The name was introduced by Plavilstshikov (1931) for aberration, so it
became valuable after Danilevsky and Miroshnikov (1985).
Clytus arietis lederi Ganglb. 1881 is a distinct subspecies
distributed in Talysh, Kopet-Dag and North Iran.
Cortodera transcaspica, Tetropium castaneum (Krasnodar), Exocentrus
stierlini and Trichoferus campestris are represented in Caucasus, the
latter also in South East Russia.
The distinguishing characters and areas of Molorchus kiesenwetteri
and M. semenovi are not clear.
Cartallum is a wrong spelling of Certallum.
Phymatodes alni alni absent in Caucasus.
Parmena balteus L. and Mallosia mirabilis Fald. absent in USSR.
Dorcadion ñinerarium F. 1787 = D. ñaucasicum Kust. 1847.
Parmena aurora must occur in Turkey.
Phytoecia hirsutula present in Turkey.
All records (Håórîwsêó,1967; Villiers,1978) of Saphanus piceus for
Caucasus are wrong.
#51
According to Danilevsky (1993b), Ph. pubescens (= Ph. glaphyra) was
usually mixed with Ph. manicata. Ph. manicata is known only from Syria and
neighbour territories and differs by spines of posterior male coxae (so
can be mixed with small Ph. cylindrica). That is why the record of Ph.
manicata for Caucasus (Danilevsky, Miroshnikov, 1985) was wrong.
Ph. pubescens is distributed in Balcan Peninsula, Near and Middle
East and is rather common in Transcaucasia. The species identity was
restored by Danilevsky and Miroshnikov (1985, as Ph. glaphyra). It is
close to Ph. icterica.
Kasatkin and Arzanov (1997) recorded Ph. pubescens (as manicata) from
Kamyshanova Poliana near Lagonahi in Krasnodar Region. According to
personal communication of Kasatkin (2002) it was based on wrong
identification of Ph. cylindrical.
According to Kasatkin (1999), Ph.pubescens is represented in North
East Caucasus (one male from Dagestan: Sulak env., 10.6.1954). It seems to
be the first reliable record of the species for Russia.
#52
In order of preliminary improvement of Cortodera taxonomy:
C. circassica is a subspecies of villosa.
C. fischtensis is a subspecies of C. alpina.
The system of Cortodera species close to C. reitteri and C. ruthena
was revised by Danilevsky (2001ab).
#53
Cortodera alpina seems to be described from Dagestan. There are
several males from Shahdag with Menetrie's labels (cotypes?) in
collections of Moscow Zoolological Museum and in collection of
M.Danilevsky. According to these specimens C. alpina and C. umbripennis
differ as subspecies of one species.
According to type materials (preserved in Budapest), C. starki is a
black parthenogenetic subspecies of C. alpina from West Caucasus.
#54
Exocentrus pseudopunctipennis was recorded for Caucasus by Lobanov et
al. (1982) without any remark, then it was recorded for Talysh
(Danilevsky, Miroshnikov, 1985) and Georgia (Danilevsky, Dzhavelidze,
1990). It was also collected in Kopet-Dag (Ai-Dere, 1985) by S.Murzin
(personal communication).
#55
Cortodera transcaspica is very numerous in Turkey and Iran and well
represented in collection of C.Holzschuh, but only by females, so it must
be parthenogenetic.
#56
According to Danilevsky (1993):
Cortodera cirsii Holz., 1975 and Agapanthia salviae Holsz., 1975 were
recorded for Transcaucasia by Kaziuchitz (1975) after wrong determination
of C. umbripennis (local black form) and A. walteri respectively.
Tetropium staudingeri ab. laticolle regardless of Podany's (1967)
opinion is not a species.
Purpuricenus sideriger is recorded for Russia.
Oberea inclusa (not a synonym of O.vittata) must be absent in Russia
and in Japan.
Pidonia malthinoides = Pidonia quercus
Leptepania okunevi = Molorchus incognitus
Chlorophorus obliteratus (described from "centralen Mongolei")= Ch.
ubsanurensis
Xylotrechus asellus = X. grumi
Agapanthia lederi (= A. helianthi) = A. lopatini
#57
Most probably Anoplodera atramentaria sibirica does not exist. I
believe that under the name Leptura (Vadonia) atramentaria sibirica
Plavilstshikov described (it was first description in his life) one of
Siberian Cortodera (both type females disappeared). His black type female
of Cortodera semenovi from Kondoma River has just same label as types of
V.a.sibirica and totally fits its decsription: Leptura a. sibirica Plav.
1915 ?= Cortodera semenovi Plav., 1936?
Possibly Plavilstshikov did not see L. atramentaria Gangl. It is very
strange that a short latin diagnosis of L.atramentaria, proposed by
Plavilstshikov (1915) without any references to materials or publications,
strongly contradicts with its original description! For example: in L.
atramentaria atramentaria: "scutello nigro ciliato", while in original
description: "Scutello dense albido-cinereo pubescente." Similar
difference in the description of elytral pubescence! But later
Plavilstshikov (1936: 344) described L.a.atramentaria exactly following
original description! Anyway, his A. a. sibirica from Altai does not
connected with Leptura atramentaria Ganglb., described after unique male
from "Kan-ssu, 18.6.1885" from G.N. Patanin materials. Holotype was
recently discovered in collection of J.Vorisek (Czechia, Jirkov) and
figured by A.Miroshnikov (1998: 397, 400). The taxon was placed in genus
Anoplodera (s.str.) by Hayashi and Villiers (1985).
#58
C.Holzschuh (1991) described from China Neoencyclops debilipes.
Following his opinion Neoencyclops differs from Grammoptera by nearly
right angle between frons and clypeus. I prefer to regard both taxa as
subgenera inside one genus. G. angustata seems to be a transitional form
both in head structure and body form.
#59
E.Vives (2000) proposed for Ropalopus clavipes (F., 1775) the oldest
name R. nigroplanus (Degeer, 1775); for Grammoptera ruficornis (F.,1781) -
G. atra (F., 1775). The changes can not be accepted according to the
Article 23.9. of ICZN (1999).
#60
G. ruficornis obscuricornis, described from Talysh, differs from
nominative subspecies by dark legs and antennae; and is isolated
geographycally.
#61
Sivana = Sieversia Ganglb. (nec Kobelt, 1880 in Mollusca). Ohbayashi
(1980) joined in one genus bicolor and Japan ruficollis under oldest name
Macropidonia Pic, 1901. I prefer to regard both species in different
genera. Kusama & Takakuwa (1984) contrary joined ruficollis with Japan
Pseudosieversia under the name Macropidonia, which also looked not
natural.
#62
Pidonia = Pseudopidonia after Hayashi (1980).
#63
A.Tcherepanov's (1979) synonymy Pidonia amurensis = P.signifera is
wrong as P. signifera (decribed from Japan) does not occur in the mainland
and absent in Russia.
#64
According to Tcherepanov (1982) X. villioni was found on Kunashir Is.
#65
Pidonia malthinoides was recorded for Korea by Danilevsky (1993d).
#66
Nivellia extensa was recorded for Mongolia (Janovsky, 1980).
#67
Pidonia amentata is represented on Kunashir Is by a subspecies P. a.
kurosawai, which must be better regarded as separate species.
#68
Necydalis gigantea was recorded for Kurile Islands (Hayashi, 1980)
#69
The list of Cerambycidae of Kirghyzstan (Ovtchinnikov, 1996) contains
some wrong data:
Kirgisiana - wrong spelling of Kirgizobia Danilevsky, 1992.
Prionus angustatus, P. turkestanicus, Apatophysis serricornis,
Molorchus kiesenwetteri, Dorcadion sokolovi (=jacobsoni), D. obtusipenne
(must be D. validipes), D. globithorax are absent in Kirgizia.
Tetropium staudingeri and T. laticolle are synonyms.
Molorchus schmidti Ganglb. 1883 = M. semenovi.
"Oberea rufipes Fisch." - such name does not exist. Possibly, the
author was going to mention Oberea ruficeps Fisch., as it was mentioned as
"subendemic". It can be the first record for the region. If so, a very
common in Kirgizia species Ph. rufipes Oliv. 1795 absent in the list as
many other Cerambycidae of Kirgizia.
#70
According to the original description: Leptura imberbis. The name was
often used in form "imperbis", possibly after Plavilstshikov (1936).
#71
The divisions of Pedostrangalia in 3 subgenera was accepted after
G.Sama (1992).
#72
According to I.M. Kerzhner (personal communication of 1986) the name
variicornis for Pedostrangalia circaocularis is invalid (secondary
homonym), but the name circaocularis (introduced as a replacement name by
Gressitt,1951) is also not good enough because several old names of
variations could be regarded as valid (niger, nemurensis). From the other
side, the replacement name, introduced before 1960 and became generally
accepted must be preserved.
#73
According to the original descriptions, the right spelling:
Dokhtouroffia and Dorcadion: dokhtouroffi, sokolowi (and the date is
1901), komarowi, tschitscherini, tenuelineatum, matthieseni, dostojewskii,
glycyrrhizae, kuldschanum.
#74
According to A.Miroshnikov (personal communication), the genital male
structures of Dokhtouroffia species are so different that they can not be
regarded as subspecies as was proposed by Kostin (1973).
#75
G.Sama (1996) described L. maculata irmasanica (from Turkey),
Hybometopia starcki ivani (from Turkey), and recognized Clytus schneidri
inapicalis Pic, 1897 (stat.n.) as subspecies.
#76
Leptura aurulenta occurs in Voronezh Region. Its larvae from
Tellerman Forest Farm collected by B.Mamaev 7.10.1958 were identified by
P. Svacha.
#77
According to Pesarini, Sabbadini (1994), Leptura annularis F., 1801
is a valid name.
#78
Leptura dimorpha described from Japan was recoded for Russia as a
species by Plavilstshikov, 1936. I've not seen such specimens from the
continent or from Russian Islands (in Japan it is common). It was also
recorded for Korea as an aberration of L.aethiops by Lee (1982) and for
Russia (without any geographical comments) as a subspecies by Tsherepanov
(1979: 370). According to Hayashi (1979) it is a subspecies, but with
impossible area including East Siberea (so sympatric with L.a.aethiops).
According to Gressitt (1951), L. aethiops = L. dimorpha. According to
Lobanov et al. (1981), Kusama and Takakuwa (1985) and Ohbayashi et al.
(1992), L. dimorpha is a species.
I believe that L. dimorpha is just a form of L. aethiops with red
prothorax, which is very numerous in Japan and rather rare on the
continent. The number of such specimens in Japan populations allow to
regard a part of Japan L. aethiops (or all) as L. a. dimorpha. The
presense of specimens with red thorax in Russia is not proven, but even if
they exist here, their rarity does not allow to join Russian populations
to L.a. doii. The situation in Korea is unclear.
Leptura aethiops seems to be never recorded from Kazakhstan, but sure
presents here at least in its easten Altai part. I.A.Kostin (1973:)
mentioned it as possible for North Kazakhstan.
#79
Oberea donceeli was originally recorded for Russia by Lobanov et al.
(1981), for Transbaicalia by Tsherepanov (1985) and for Mongolia by
Namhaidorzh (1979).
#80
Strangalia attenuata and Oberea depressa were recorded for Mongolia
(Janovsky, 1977).
#81
Cortodra pumila was recorded for Rostov (1.6.1954) by Ju.Arzanov et
al. (1993). According to D.Kasatkin (personal communications, 2000-2002),
there are Cortodera pumila (Krasnyi Sulin) and Ph.(H.) millefolii
(Persianovka, 1 05 2001, D.Gapon leg.) in Rostov Region and Stenurella
novercalis (males with black abdomen) in North Caucasus (Bolshaia Laba
Valley).
#82
According to (Danilevsky, Dzhavelidze, 1990), S. b. limbiventris is
regarded as a subspecies distributed in Adzharia and Turkey; S.
septempunctata anatolica (known from Turkey and Bulgaria) is represented
in Transcaucasia.
#83
According to Kusakabe, Ohbayashi (1992), J. bangi and J. znojkoi are
different species, and J. bangi, distributed in Japan, seems to be absent
in Russia.
#84
According to A.Villiers (1978) and E. Vives (2000), Judolia
sexmaculata parallelopipeda (described from Dauria and Amur River) is an
easten subspecies. According to my materials it is distributed eastwards
Urals. The forests of south Urals (Iuriuzan env.) are occupied by J. s.
sexmaculata. The western most locality of J.s. parallelopipeda must be
Petropavlovsk env. (Kostin, 1973) and Jamal Peninsula (Shchuchie), then
Tuva Republic.
#85
According to A.Bartenev (personal communication,1982), Pachytodes
erraticus absent in Crimea.
A.Kaziuchitz (personal communication,1984) had 10 specimens from
Crimea Peninsula.
#86
According to J.Vorisek (personal communication, 1992), the original
description of Strangalia connecta is the evidence of its synonymy with
Pachytodes cometes.
#87
According to Danilevsky (1988d): Oedecnema dubia (F., 1781) nom.
praeocc. (non Scop., 1763) was changed by Silfverberg (1977) to O. gebleri
(Ganglb., 1889)
#88
According to Danilevsky, who studied in 1992 the type of Grammoptera
japonica in Paris, it is Alosterna chalybeella.
#89
B.Namhaidorzh (1972) recorded for Mongolia: Eodorcadion lutshniki, E.
humerale ssp. humerale, E. humerale ssp. impluviatum.
B.Namhaidorzh (1974) recorded for Mongolia: Anoplodera rufiventris,
Hesperophanes heydeni, Cleroclytus collaris, Oberea inclusa.
B.Namhaidorzh (1976) recorded for Mongolia: Alosterna tabacicolor
erythropus (as bivittis), Saperda perforata, Saperda scalaris, Eumecocera
impustulata, Nupserha marginella.
B.Namhaidorzh (1979) recorded for Mongolia: Phytoecia ferrea (as
mannerheimi).
#90
A. ingrica (decsribed from Luga) is a species (Karpinsky, 1948 and
others), which is not known eastwards Orenburg. It is not connected with
Leptura erythropus, described from Altai. The original description of the
latter totally fits to A. tabacicolor from Altai. Local A.tabacicolor is
now regarded as A.t.bivittis, which was described from the area eastwards
Baikal, so A. tabacicolor erythropus (Gebl.1841) = A.t.bivittis (Motsch.
1860), or represents a separate subspecies from Altai, as well as A.t.
plavilstshikovi can be a separate subspecies from Tuva.
#91
S.Bobrov (Ivanovo) collected A.ingrica in Arkhangelsk Region (Pinega
Nat.Res., 8.1991).
#92
According to Danilevsky (1992b):
Anoplodera rufihumeralis occurs in Primorie (male and female in
collection of Jaroslav Dalihod (Svobody 676, 27200 Kladno, Czechia).
Grammoptera elegantula = Pseudalosterna orientalis.
Cylindilla grisescens = Atimura askoldensis
Oberea atropunctata was collected in Primorie by Uno Roosileht and M.
Kruus (Estonia); male in collection of M.Danilevsky.
#93
Using Miroshnikov's (1998) publication:
I accept his transform of Palaearctic Anoplodera rufiventris and A.
baeckmanni to Nearctic genus Xestoleptura, which was supposed before by
Svacha (1989: 19).
I include in Aredolpona (=Corymbia): rubra, dichroa, variicornis and
absent in Russia fontenayi. Other members of Corymbia sensu Miroshnikov
(until better decision) are included in Paracorymbia, as well as
Melanoleptura as a subgenus.
Paracorymbia = Batesiata.
Brachyleptura Casey, 1913 and Stictoleptura Casey, 1924 are
represented only in America, as well as Megaleptura Casey, 1913 = Stenura
Dejean, 1837 (not Stenura Cuvier,1820, Aves).
According to E.Vives (2000) Corymbia Gozis, 1886 is a junior
homonym of Corymbia Walker, 1865 (described in Noctuidae, now in
Notodontidae) and must be replaced by Aredolpona Nakane et
Hayashi, 1957.
The necessaty of the name change is evident as Corymbia
Walker is not "nomen oblitum" according to the Article 23.9.1. of
ICZN (1999) and was mentioned among valid names in "The Genera
Names of Moths of the World." Vol.2. London. 1980: 44 (by Watson,
A., Fletcher, D.C. and Nye, I.W.B. in Nye I.W.B.).
#94
Paracorymbia apicalis was described from South Siberia (as Leptura).
Two syntypes are preserved in Moscow Zoological Museum (both without head
and prothorax). The beetles seem to be close to P. fulva, P. tonsa, P.
pallidipennis.
#95
According to J. Vorisek (personal communication, 1992), P. rufa is
represented in Caucasus and Turkey by P.r. dimidiata (Daniel, 1891). But
according to the original description, "dimidiata" is characterized by
black elytral half (or 2/3); such form is uknown in Caucasus.
The specimens, similar to Caucasian variations, were identified in
Paris Museum as var. attaleiensis Dan.
#96
According to G.Sama (1991):
Leptura ustulata Men., 1832 (nec Laicharting, 1784) must be replaced
with Leptura heydeni Ganglbauer, 1889.
Plocaederus Dejean,1837 (not Thomson, 1860) was introduced for South
American species, so African P.cyannipennis can not be its type species.
P. bellator Serville, 1834 is designated as type species and the genus
became totally American. For Plocaederus sensu Thomson, 1860 with type
species P. cyanipennis, 1860 was proposed a new name Neoplocaederus.
Cerambyx velutinus Brulle, 1832 (nec F., 1775) - was replaced with C.
welensii Kuster, 1846.
Cerambyx fulvum Villers, 1790 (not Scop. 1763) was replaced with
Callidium unicolor Oliv., 1795.
Callidium speciosus Ad., 1817 (not Schneider, 1787) was replaced with
Plagionotus bobelayei Brulle, 1832.
Morimus Serville, 1835 = Morinus Brulle, 1832 (type sp. is designated
as - lugubris F., 1792 = asper Sulzer, 1776).
Stenidea Mulsant, 1842 = Deroplia Dejean, 1837 (type sp. is
designated as genei Aragona, 1830).
Stenostola is attributed to Dejean, 1835.
#97
According to the study of the type of Leptura dichroa in Paris: L.
dichroa = Aredolpona succedanea (as it was intoduced by Gressitt,1951).
#98
According to J.Vorishek (personal communication,1992), P.l.livida
does not occur eastwards France; in Italy - P.l.pecta; in Greece, Black
sea coast of Bulgaria, Transcaucasie and Turkey - P. l. desbrochersi Pic;
but near Sochi - P.l. pecta.
#99
Necydalis xanta Sem. was described as variation of N. major with
yellow head, prothorax, legs and abdomen from near Novorossiisk. Later
(Semenov,1902) it was regarded as a species. According to Plavilstshikov
(1936) it is a synonym of N. ulmi. Without study the type I prefer to
return the original position (I've got N.major from Gantiadi).
According to several specimens collected in Khosrov (Armenia) by
V.Dolin and preserved now in collections of Danilevsky and Murzin, N.ulmi
mesembrina does not differ from European forms.
#100
Niisato (1994) recorded Necydalis major aino for Mongolia. Siberian
populations must be compared with Eyropean ones.
#101
The name Aseminae Thomson, 1864 must be replaced with Spondylidinae
Serville, 1832 becouse of priority. The correct spelling is accepted after
Vives (2000), as well as Spondylidini.
#102
Drymochares starcki was recorded for "Crimee" by Sama and Rapuzzi
(1993: 278 in "Resume"), which had to be a mistake, as the locality was
not shown on the map (:293) or discussed in the text of the article.
The original spelling is: Drymochares starcki and Hybometopia
starcki.
#103
According to I.Zahaikevitch (personal communication,1982), Saphanus
piceus Laich. was collected in Ivanovo-Frankovsk Region of Ukraine. The
species was mentioned for USSR by Zahaikevitch (1991).
S. piceus collected in Turkey is preserved in collection of S.Kadlec.
#104
U.R. Martins (1980) placed Turcmenigena in Hesperophanini, and Myctus
in Atimiini.
#105
Atimia maculipuncta was recorded for Mongolia (as Myctus) by Lindeman
and Lyamtseva (1979). A. maculipuncta from China and Mongolia differs from
A. nadezhdae from Russia, so better to regard the latter as a subspecies,
but not as a synonym as it was proposed before (Lobanov et al., 1981).
#106
I.Zahaikevitch (1991) proposed:
Mesocerambyx (not Mesocerambyx Breun.et Hitzinger, 1943), that must
be a synonym of Microcerambyx Miksic et Georgijevic, 1973.
Hylotrupini and Nothorhinini - the latter seems to be not necessary,
as well as accepted by him Exocentrini Pascoe, 1864.
#107
According to J.Vorisek (personal communication,1992), the east
populations of Asemum striatum are characterized by rough elytral
sculpture. So, the existence of the east subspecies can be accepted, but
the name A.striatum amurense Kr.is younger than Asemum subsulcatum
Motsch.1860: 152 ("Nord de la Siberie").
#108
According to J.Vorisek (personal communication,1992), T. gracilicorne
from Ilmen Nat. Reserve (South Urals) is represented in his collection. It
is the most western locality of the species (if T. gabrieli and T.
gracilicorne are really different species, becouse no reliable differnces
is observed - M.D.).
#109
Asemum tenuicorne was recorded for Spain by E.Vives (2000b), as well
as T. fuscum (Sanchez, Tolosa, 1999), but according to Vives (2000) the
last record was based on wrong determination of A.tenuicorne.
#110
Pogonocherus ovatus from the territory of the USSR is unknown. All
specimens of the species in Plavilstshikov's collection are from the West
Europe.
According to Bartenev (personal communication, 1982),he proved for
Crimea: Tetropium castaneum, Obrium brunneum, Pogonocherus ovatus,
Phytoecia faldermanni.
#111
After Silfverberg (1979): A.rusticus = A. tristis.
Sama (1991) also excepted identity of the type of Callidium tristis
F., 1787 and rusticus L., 1758, but Lipp (1937) declared identity of
tristis and ferus Mulsant, 1839. Evidently, different type specimens
exist. Is it possible to except Lipp's opinion as first?
#112
Tetropium aquilonium was recorded for Sweden and Finland (Lundberg,
1993).
#113
The tribe Apathophysides Lacordaire, 1869 was originally rased to
subfamily level by Danilevsky (1979).
#114
Ïîäðîä Protapatophysis Sem. et Schegol.-Bar. 1936 (type sp.: A.
kashmiriana Sem.) includes A. montana Gah., but described later A.
pavlovskii belongs to the nominative subgenus because of widely separated
female posterior coxae (up to 2001 only one female seems to be known -
Danilevsky, 1979) and poorly developed male tarsi pads.
#115
Icosium tomentosum atticum was recorded for Azerbaidzhan by M.Slama
(1999) after one specimen (Zerat,Bezh Barma,19.5.1975, Fr.Navratil leg.).
#116
According to Sama (1994d), Trichoferus holosericeus (Rossi, 1790) =
T. cinereus (Villers, 1789), described as Cerambyx (not Cerambyx cinereus
De Geer, 1775)
#117
Trichoferus griseus, described from Africa, was usually mixed with T.
fasciculatus described from Transcaucasie and was never reliably recorded
for USSR or Russia.
T. griseus from Crimea (only females) seems to be preserved in
collection of M.Danilevsky.
#118
A.Brinev collected one specimen of Ph. semipunctata in Tzihizdziri
(8.1990, Kobuleti distr. of Georgia) - preserved in Moscow Pedagogical
University.
#119
According to Hudepohl (1990), Neocerambyx Thomson,1860 = Mallambyx
Bates, 1873. Neocerambyx raddei was often regarded as Massicus Pasc.,
1867.
#120
Cerambyx velutinus was definitely recorded for Transcaucasia by
Plavilstshikov (1955: 512). According to Pavlov-Verevkin (personal
communication to A. Lobanov, 1984), C. velutinus was collected by him in
Georgia (Mtzheta) and preserved in his collection.
#121
According to J.Vorisek (personal communication, 1992), C. cerdo
klinzingi, described from Caucasus is a good species, described later as
C. heinzianus.
#122
Dissopachys pulvinata was recorded for Azerbaidzhan by Sama (1999):
Iardymly, Avash, 1200-1500ì, 14.6.1996, 38"50N,48"10E, leg. W.Schwalller.
#123
Rosalia coelestis houlberti Vuillet, 1911 (Tibet) is a separate
species (Gressitt, 1951).
#124
Lobanov et al. (1982) indicated the wrong dates for Purpuricenus
talyshensis Rtt.,1891 (as 1914) and Callidium F., 1775 (as 1777).
#125
Purpuricenus lituratus = petasifer, accepted after Kusama & Takakuwa
(1984).
#126
The taxonomy of Asias close to A.halodendri is not clear. It was
evident mistake to regard all populations from European Russia to Far East
as one species without any subspesies, as it was proposed by Namhaidorzh
(1972).
The differences between European and Far East populations are
evident, so the name A. halodendri halodendri can not be used for east
populations, as Cerambyx halodendri Pallas, 1776 was described "... ad
Irtin" (= Irtysh), and the specimens from Kazakhstan are not close to Far
East populations.
As it was declared by Kostin (1974), populations from East Kazakhstan
differs from West Kazakhstan populations at the subspecies level. I
preliminary accept that A. halodendri ephippium (Steven et Dalman, 1817),
described from South Russia (Terek River), is distributed from North
Caucasus to the south part of European Russia (northwards to about
Saratov) and in Ural Region of Kazakhstan.
In Semipalatinsk region Asias halodendri halodendri is distributed.
For far east Maritime subspecies, which penetrates far in East
Siberia, the name Asias h. pirus (Arakawa, 1932) can be used. It was
introduced for Korean population as Purpuricenus pyrus.
Rather peculiar specimens from Tuva were described as Anoplistes
minutus Hammarstroem, 1893 - same in Mongolia.
According to Namhaidorzh (1972): "In low, south areas of Mongolia as
well as in neighbour China a small, pale, pubescent form, described as A.
kozlovi, occurs." (Lectotype was designated by him).
From South-East Kazakhstan Purpuricenus (Asias) heptapotamicus
Semenov, 1926 was described. Several rather strange specimens from near
Balkhash Lake and from Tarbagatai (collection of M.Danilevsky) possibly
belong to this form.
The proposal of Kostin (1974) to regard A. jacobsoni (Valley of Syr-
Daria River) as subspecies of A. halodendri seems to be a mistake.
#127
According to J.Vorisek (personal communication, 1992), Asias
jomudorum = Asias chodjaii Holz. 1974
#128
Aphrodisium = Tomentaromia - the synonymy was published by Gressitt
et al. (1970).
#129
Aphrodisium faldermannii was recorded for East Siberia by Reitter
(Wien. Ent. Ztg., 1906, 25: 277) - after Gressitt, 1951: 202; and supposed
for Mongolia by Namhaidorhz (1972).
#130
Axinopalpis gracilis christinae Rapuzzi, 1996 was described from
Pelopones, Mt. Taigetos.
#131
D. starcki ivani Sama & Rapuzzi, 1993 and D.s. cavazzutii Sama &
Rapuzzi, 1993 were described from Turkey.
#132
The tribe Stenhomalini was described by A.Miroshnikov (1989: 742).
According to A.Miroshnikov (1989) Stenhomalus lighti Gress. was found
by S.Belokobylsky in S Primorie. S.lighti = S. vulcanus Tsher.
#133
Obrium obscuripenne (according to Villiers, 1978) = O. graciliforme
Lipp, 1939 = O. gracile Plav., 1933 (non O. gracile Krynicki, 1832).
#134
According to Danilevsky (1988d):
Chlorophorus sexmaculatus (Motsch., 1859), nom. praeocc. (non
Donovan, 1805) was changed to Ch. simillimus (Kraatz, 1879) by M.Hayashi
(1983).
Tetrops elaeagni = T. plaviltshikovi
#135
According to Kusama & Takakuwa (1984), M. minor fuscus is distributed
on Hokkaido and Kunashir. Sakhalin is apparently occupied by nominative
subspecies.
#136
The taxonomic situation with Molorchus in Transcaucasia rests
inclear. My series from near Tbilisi (Manglisi: a male and two females)
looks very close to M. juglandis Sama, 1982 (described from S Turkey).
According to personal communication by J.Kratochvil (Febr. 1986) to
A.Lobanov: Molorchus minor monticola Plav. 1931 = M. rufescens
Kiesenwetter, 1879, described from Borzhomi. So, it seems possible that M.
rufescens Kies. 1879 = M. juglandis Sama, 1983 = M. monticola Plav., 1931.
The name "monticola" was addressed to Danilevsky et Miroshnikov
(1985) by Danilevsky in Svacha, Danilevsky (1988: 205), as allegedly
originally introduced as infrasubspecific. But the title of
Plavilstshikov's description is: "4. Molorchus minor L. var. monticola
nova.", but in the text: "Wie es scheint , nicht eine Aberration, sondern
eine Morpha (forma alpina)." So the word "Morpha" sounds, but formally it
was described as variation, and I regard now M.m.monticola Plav. as valid.
I've found a pair of M.monticola from Turkmenia (Krasnovodsk,
10,13.4.1899) in Zoological Museum in St.-Petersburg and one female from
Kara-Kala is in my collection.
#137
The original spelling was "Linomius". "Limonius" was used only by
Villiers (1978).
#138
According to Villiers (1978: 276 ): M. kiesenwetteri = M. plagiatus.
#139
According to Sama (1995):
M. marmottani absent in Russia;
M. m. crovatoi Sama, 1995 (Italy) and M. m. frischi Sama, 1995
(Turkey) are described.
M. plagiatus is recorded from Iran.
M. schmidti = salicicola = semenovi;
M. kiesenwetteri ssp. hircus (for Caucasus and Turkey) =
M.anatolicus.
#140
K.Adlbauer (1992) firstly recorded for Turkey: Molorchus marmottani,
Isotomus speciosus, Anaglyptus persicus and Pogonocherus hispidulus.
#141
According to Kusama and Takakuwa (1984):
M. ishiharai = M. kobotokensis kunashiricus, that agrees with
Danilevski's materials from Kunashir.
According to A.Lobanov (personal communication, 1987), the holotype
of Molorchus kobotokensis kunashiricus was lost in Novosibirsk. It is also
absent in the list of Coleoptera types preserved in the Musem
(Tshernyshev, 1997).
#142
M.Danilevsky saw several Molorchus kobotokensis from Far East Russia
(Kaimanovka, 15.6.1979, Czech collector) in C.Holzschuh's collection. No
differences from Japan specimens were observed (1993).
#144
Glaphyra heptapotamica (Plav.) was recorded for China (Ningxia-Hui;
Wrzhong) - Hua L.Z., Niisato T. (1993), but the record could be connected
with G. alashanica Semenov-Tian-Shanskij, Plavilstshikov, 1936 or with a
new species.
#145
According to my study in Zoological Museum of St.-Petersburg (2001) of a
big series of Nathrioglaphyra heptapotamica from Ili valley (Kapchagai),
Ural valley (Ianvartzevo), Aiaguz, Dzhezkazgan, Talasskiy Alatau (Daubaba)
- N. heptapotamica = Molorchus amygdali. N. heptapotamica (as
Molorchus) was recorded for Russia (Orenburg environs, Utvinskoe in
Krasnokholms forest farm) by Tsherepanov (1981).
In the Museum a series of N. heptapotamica is identified by
Namkhaidorzh as Molorchus alashanicus Semenov-Tian-Shanskij,
Plavilstshikov, 1936. Its original description was based on unique female
from: "Mongolia australis: jug. Alashan, angustiae Tso-sto", which had to
be preserved in Zoological Inst. (St.-Petersburg), but was not found there
by me. M. alashanicus seems to be never recorded for Republic of Mongolia,
so only original description seems to be available also for Namkhaidorzh.
I've studied two specimens of Glaphyra from China ("Chekiang, Tien-Mu-
Shan, 15.5.37 and 14.6.37, E.Suenson leg."). First is male, second seems
to be a female because of short antennae (abdomen totally masked by hind
wings). Both have same colour as N. heptapotamica, but differs from it
considerably. Prothorax is much longer with three elongated shiny areas
(as in M. alashanicus), elytra with rough but rather scattered
punctuation; antennae in male much longer than body (surpassing abdomen by
at least two apical joints), in female a little longer then body; while in
N. heptapotamica male antennae slightly longer than body and in female
much shorter than body.
In general this pair is more or less fitting to the description of M.
alashanicus, but the distance between their localities is about 1500km.
Unfortunately antennal characters are totally omitted in the original
description of M. alashanicus (only one "character" was mentioned: "Par la
conformation de ses antennes cette espece appartient au groupe des especes
voisines du M. kiesenwetteri Muls.") Antennal length in the pair from
Chekiang is really similar to M. kiesenwetteri and 3d-4th joints are
relatively short, a little shorter than 5th , but 1st joint is very
unusual - very short, shorter than 3d and strongly swollen (only two times
longer than wide). Sill I preliminary identify this pair as M.
alashanicus.
#146
According to J.Voricek (personal communication, 1992), Stenopterus
rufus in Turkmenia is represented by S. r. transcaspicus Plav.
#147
According to A.Kaziuchitz (personal communication, 1984) he had in
his collection Stenopterus ater from Crimea. The species was also recorded
for Crimea by Bartenev (1989).
#148
According to I.Kerzhner (personal communication, 1985), Callimus
Muls., 1846, was not preoccupated in Orthoptera, as Callimus Fisch.-Wald.,
1830 is wrong posterior spelling of Callimenus F.-W., 1830. So,
Callimellum is not valid.
#149
The name "Protocallimus" used by Plavilstshikov (1940: 173,661) and
then by Danilevsky and Miroshnikov (1985) seems to be just a wrong
spelling of Procallimus Pic.
#150
The published type locality of Certallum ebulinum is France.
But the species description was based on black-pronotum specimen.
Such specimens are known from Spain as very rare and seem to be
possible in France (Villiers, 1978: "Seule la morpha ruficolle
SEMBLE se rencontrer en France, :"). Such situation caused the
supposition of wrong definition of type locality by Linnaeus
(Villier, 1978; Sama, 1988). Sama (1988: 83) supposed the real
locality of type specimen in North Africa and accepted Certallum
ebulinum ssp. ruficolle (described from Italy) distributed from
Iberian Peninsula to Caucasus and Iran. But I do not see the base
for such supposition. The type specimen could really be collected
in Europe and then C. ebulinum = C. ruficolle.
#151
Original spelling is "Ropalopus".
#152
R.fischeri, described from Central Russia, differs considerably from
both European species (closer to R.insubricus). I prefer to regard it as a
separate taxon until the revision of the group.
#153
Ropalopus macropus from Caucasus are often designated in European
collections as R.caucasicus. The main distinguishing character are spines
on first antennal joints. But the development of antennal spines is rather
variable both in European and Caucasian populations. I do not see any
differences between them.
According to Plavilstshikov (1940), R. clavipes = R. caucasicus.
#154
Ropalopus varini Bedel, 1870 = R. spinicornis (Abeille, 1869),
described as Callidium (not C. spinicorne Olivier, 1795).
#155
Pronocera brevicollis Gebler, 1833 (nec Dalman, 1817).
#156
According to A.Miroshnikov (personal communication, 1993),
Callidiellum rufipenne was found near Sochi (imago and larvae in
Cupressus).
#157
According to Zahaikevitch (personal communication, 1983), Semanotus
undatus must be included in Crimean fauna after one specimen (from
Livadia) from V.Shavrov's collection.
#158
Several species were definitely recorded fore Mongolia by Janovsky
(1974): Anastrangalia renardi (Khubsugul and Ara-Khangai aimaks),
Callidium aeneum (Khubsugul, Baian-Ulegey, Kobd aimaks), Xylotrechus
altaicus (Ubsunur aimak), Amarysius sanguinipennis (Selenga aimak),
Leiopus albivittis (Selenga and Khubsugul aimaks).
#159
According to J.Voricek's opinion of 1992, C. aeneum in NW Georgia and
West Caucasus is represented by C.a.longipenne Plav.
#160
Phymatodes Mulsant,1839 (not Phymatodes Dejean, 1834 - Tenebrionidae)
was conserved by ICZN (1989).
#161
Phymatoderus Dejean, 1937 is nomen nudum, so Phymatoderus Reitter,
1912 = Reitteroderus Sama, 1991;
#162
According to J.Voricek's opinion of 1992, south of Ukraine (Donetzk
Region and Crimea) and Caucasus are occupied by Ph. pusillus rufipenne.
Nominative subspecies is distributed in West Europe and West Ukraine.
#163
According to Niisato (1995), Phymatodes infasciatus Pic, 1935 =
vandykei Gress. 1935 = ussuricus Plav. 1940.
#164
According to E.Vives (2000) Paraphymatodes fasciatus (described as
Cerambyx fasciatus Villers, 1789, not Scopoli, 1763, not Degeer, 1775, not
F., 1775, not Geoffroy, 1785, not Villers, 1789) must be replaced with P.
unifasciatus (Rossi, 1790). The necessaty of the name change must be
checked in agree with Article 23.9.1. of ICZN (1999)
#165
Pogonocherus ressli and Phymatodes alni ebursensis were recorded for
Talysh by A.Miroshnikov (2001).
#166
The system of Cleroclytus was revised by Danilevsky (2001d).
#167
According to the opinion of Zahaikevitch of 1983, Dorcadion tauricum
and Anaglyptus mysticus absent in Crimea, because of the absence of any
data.
#168
According to Miroshnikov(2000), Anglyptus ganglbaueri = A. persicus =
A. natae; all records of A. mysticus for Caucasus concern A. misticoides.
Plavilstshikov (1940) as well as Danilevsky and Miroshnikov (1985)
wrongly mentioned the author of A. persicus Pic, as "Pic et Reitter".
#169
Oligoenoplus rosti was regarded as Cyrtophorus rosti by Kusama and
Takakuwa (1984).
#170
According to J.Voricek's opinion of 1992, Plagionotus detritus is
represented in north and west Caucasus by P.d.caucasicola Plav.
#171
According to Sama (1994):
Plagionotus = Echinocerus, but I prefer to regard them as separate
genera.
Turanoclytus gen. n. for Xylotrechus namanganensis (original spelling
is "namaganensis", but "namanganensis" is now in prevailing usage
according to the Article 33.3.1 of ICZN, 2000) - typus generis and X.
asellus, but for me Xylotrechus = Turanoclytus.
Type species of Acanthoderes is Lamia daviesi (Thomson des., 1864)
from C and S America, and European species belong to another genus -
Aegomorphus. Same was done by Linsley et Chemsak,(1985) for American
Acanthoderes.
According to Monne (1994), the type species of Acanthoderes is Lamia
varia F.,1787 = Acanthoderes clavipes (Schrank, 1781), designated by
Bates, 1861 (but not S American Lamia daviesi, designated by Thomson,
1864).
In fact the text by Bates (1861: 19): "In A. varius, the
European species which may be considered typical of the genus,:"
can not be regarded as the type designation of the genus.
#172
According to Burakovski et al. (1990) Echinocerus Muls.,1863 is a
junior homonym of Echinocerus White, 1848 (Crustacea). The new name is
necessary.
#173
Echinocerus scalaris was recorded for Caucasus (Lopez-Colon, 1997)
without any reasons.
#174
Ch. obliteratus was recorded for Mongolia by Heyrovsky (1965).
Ch. mongolicus Pic, 1943, described from "Mongolie" was mentioned by
Namhaidorzh (1972) as a separate species. One specimen with such
identification is preserved in Heyrovky's collection (Prague) and looks
very similar to my 3 males of Ch. obliteratus from Mongolia. Evidently
that specimen was compared with Ch. diadema kaszabi in its original
description.
The dark elytral patterns in all my three Mongolian specimens (from
rather distant localities: Gobi-Altai aimak, South-Gobi aimak, Kobd aimak)
are a little different. The last specimen (with more reduced dark elytral
pattern) is totally agree with the picture of Ch. ubsanurensis in
Tsherepanov's(1982) monograph. Most probably Ch. obliteratus = Ch.
mongolicus.
The dark elytral pattern in Ch. obliteratus looks like reduced black
patterns of typical Ch. diadema. That is why such specimens were
described, as Ch. diadema kaszabi. The original description of Ch.d.
kaszabi totally fits to some of my specimens of C. obliteratus. So it
looks possible that Ch. obliteratus is a subspecies or just a colour form
of Ch. diadema.
I am sure same taxon was recorded for Mongolia as Ch. faldermanni (by
Heyrovsky, 1968 for Kobd aimak, Khara-Us-Nur and independently by
Namkhaidorzh, 1976 for South Gobi-aimak, 20km S Bulgan).
Ch. diadema diadema was also recorded for Mongolia (Namkhaidorzh,
1974 1976). It is also represented by two specimens in my collection
(South-Gobi aimak and Baian-Khongor aimak). Mongolian Ch. d. diadema is
very close by all characters to Ch. d. diadema from Far East Russia.
#175
First records for Mongolia: Chlorophorus ubsanurensis - Gobi-Altai
aimak, Baian-Khongor aimak, Agapanthia leucaspis - Selenga aimak
(Namhaidorzh, 1982).
#176
A.leucaspis = A. euterpe (my study of A. euterpe type in Zoological
Museum of Moscow University). The synonymy was published by Tsherepanov
(1984).
#177
Rhaphuma is characterized by long 3d antennal joint, spaced out
antennal bases and others.
#178
According to Kusama and Takakuwa (1985): Xylotrechus = Xyloclytus =
Rusticoclytus.
#179
Redescription and new locality data of Xylotrechus polyzonus in
Primorie Region were published by Murzin(1981)
#180
According to Miroshnikov (1990) Clytus stepanovi Danil.et Mirosh.
1985 (stat.n.) is a species (it was described as C. vesparum stepanvi).
#181
After type materials study in Plavisltshikov's collection (1986) I
regard:
Clytus raddensis = C. hypocrita.
Clytus arietoides = C. venustulus = C. nigritulus.
#182
My preliminary opinion about type of Clytus nigritulus Kr. (#181) was
probably connected with a mistake as the cotype of this specis in Paris is
very similar to C. fulvohirsutus, but not arietoides. It is necessary to
check once more the Kraatz's type in Eberswalde.
#183
Paracorymbia fulva is reliably known to me (1991) from Belarus and
Kharkov region (Ukraine). It was recorded for Belarus by Aleksandrovitch
ey al. (1996).
#184
Palimna liturata continentalis was regarded by Plavilstshikov (1958)
as a synonym of the nominative subspecies from Japan, but as a separate
taxon by Gressitt (1951)
#185
Olenecamptus octopustulatus was recorded for Transbaicalie (Tchikoi -
borderline with Mongolia) by Tcherepanov (1983), so old records for the
taxon for Mongolia (ignored by Plavilstshikov, 1958) could be right.
Some Japan authors (Kusama and Takakuwa, 1984; Ohbayashi et al.,1992)
regard Ibidimorphum Motschulsky in Schrenck, 1860 (and so Olenecamptus
octopustulatus Motschulsky in Schrenck, 1860) as nomen nudum and accept
the description Motschulsky in Blessig, 1873. But the description of 1860
looks valid with type locality and colour picture.
#186
Olenecamptus mordkovitshi was described after one specimen (with
brown unicoloured elytra without spots) from near Tchita ("Nizhniy
Tsasuchei").
#187
I do not see conciderable differences between Pterolophia mandshurica
and P. angusta (Bates, 1873) from Japan (the details of punctuation are
usually different and elytral tubercles of P.mandshurica are usually more
developed). Both taxa could be regarded as subspecies. Possibly P. maaki
also has very close Japan taxon (P. kaleea?).
#188
According to Tsherepanov (1983):
Pteroplophia mandshurica = selengensis (described from Mongolian part
of Selenga River Valley. Holotype and a paratype of P. selengensis are
preserved in Zoological Museum (St.-Petersburg). In general they are a
little paler than specimens from Far East Russia, but no other
differences.
Egesina bifasciana was found on Sakhalin, Microlera ptinoides was
found on Kunashir. The latter is also recorded by Tsherepanov for Taiwan,
may be on the base of doubtful data of Gressitt (1951). According to
Nakamura et al. (1992), M. ptinoides absent in Taiwan.
Microlera ussuriensis sp.n. was described from Ussuri Land and later
separated in a new genus Pseudomesosella Miroshnikov, 1989 (Apodasyini).
As it was mentioned by Tsherepanov (1983: 134), the records of
Acalolepta fraudatrix for Kunashir by Danilevsky and Kompantzev (1979) and
possibly by Krivolutzkaia (1973) were concerned Japanese A. sejuncta,
which is also known from Sakhalin, Korea and possibly from Russian
mainland (Danilevsky, 1998a). But Acalolepta fraudatrix was recorded for
Kunashir by Kusama & Takakuwa 1984.
#189
I regard Pterolophia mandshurica = burakowskii on the base of
original description accompanied by a picture. P. burakowskii was
described from East-Gobi Aimak. I've got a female of Mongolian P.
mandshurica from Bulgan Aimak. It was originally recorded for Mongolia by
Namkhaidorzh (1974: 173 - Sukhe-Bator Aimak, East Aimak, East-Gobi Aimak)
as P. rigida. Later (Namkhaidorzh, 1976: 213) the identifications of
corresponding specimens were changed to P.burakowskii.
#190
I've got in my collection one specimen of Apomecyna histrio with the
label: "East Siberia, Selenginsk, 1914".
#191
Following Plavilstshikov (1958), we (Lobanov et al., 1982) used wrong
spelling "Pterycoptini" of Ptericoptini.
According to Breuning (1960) the tribe Apomecynini includes
Ptericoptini with genus Xylariopsis). The genus Mimectatina (=Doius) was
placed in his Rhodopini (in my list Apodasyini) or in Rhodopinini
(Breuning, 1975).
Several authors regard Doius close to Xylariopsis and placed both in
separate tribe Ptericoptini (Gressitt, 1961, Tsherepanov, 1984)
#192
Rhodopinini seems to be composed of one genus only. Rhodopina is
closed to Lamiini. According to Linsley and Chemsak (1985), Desmiphorini
(the name was accepted by Vives,2000 for Anaesthetis and others) is rather
special and includes only American genera. Other genera of Rhodopinini
(sensu lato), often included in Apodasyini, are not close to each other
and composition of the tribe is artificial (Miroshnikov, 1989).
#193
The synonymy: Microlera ussuriensis Tsher. = Miaenia florovi Tsher.
was declared by A.Lobanov (personal communication of 1987) on the base of
holotypes study of both taxons and was published as possible by
Miroshnikov (1989) on the base of original descriptons. Then it was
published by G.O. Krivolutzkaia (in: Tsherepanov, 1996: 121) on the base
of A.Lobanov's opinion.
#194
According to Vorisek (personal communication of 1992), Armenien
Stenidea genei is possibly S.g.naviauxi Villiers, 1970 described from
Iran.
The species was recorded for Stavropol Region (Mashuk Mt.) by
Kasatkin and Arzanov (1997).
#195
Sophronica obrioides (described from Japan) was primary recorded for
Russia by Plavilstshikov (1932: 194) as Lasiapheles obrioides Bates and
then by Samoilov (1936: 233). Tsherepanov's (1984: 49-50) record was
connected with wrong identification of Ussurella napolovi (Danilevsky,
1995). Very possible that two first records were also based on U.napolovi.
So, S. obrioides most probably absent in Russia as well as on the
continent.
#196
The genera Deroplia (= Stenidea) and Oplosia were placed by Breuning
(1963) in Rhodopinini ("Rhodopini"). It is generally accepted position (in
our list - Apopasyini). But in the revision of "Asiato-Ausralienne"
Rhodopinini (Breuning, 1975) both genera are absent. May be the author
regarded them as not quite "Asian"?
Oplosia was placed in Acanthoderini by Linsley, Chemsak (1985). This
position can be proven by larval characters (Mamaev, Danilevsky, 1975;
Svacha, 2001).
Mimectatina = Doius (see Breuning, 1963).
#197
Terinaea atrofusca = Miania tiliae: the synonymy was published by
G.O. Krivolutzkaia (in: Tsherepanov, 1996: 121)on the base of the personal
communication of S. Murzin.
According to personal communication of S.Murzin of 1986, T. atrofuca
tiliae is a continental subspecies.
#198
According to Miroshnikov (1989), Mimectatina divaricata was found on
the continent (about 20km SE Ussurisk, 29.8.78, Kasparian leg.). The
author prefers to regard Doius as a separate genus.
Exocentrus lineatus was found on the continent (Nakhodka, 20.8.85,
Belokobylsky leg.).
Cornumutila quadrivittata was found on Kamtchatka Peninsula
(Kozyrevsk, 7.85). Following Tsherepanov (1979), the author regards
C.quadrivittata = C.semenovi.
Miccolamia "verucosa" (in fact M.glabricula) was found in S Sakhalin
(Kholmsk, Dolinsk).
#199
Rh. schurmanni Breun., 1969 was found in Talysh by M.Danilevsky
(1982). Once (Breuning, 1975) the species was wrongly spelled as Rh.
schuberti.
#200
According to Hasegawa and Ohbayashi (2001), Miccolamia verrucosa
absent in Russia; it was recorded before on the base of wrong
determination of M. g. glabricula, distributed in Japan, Sakhalin and
Kurile Islands.
#201
E.Vives (2000) accepted the original spelling Aplocnemia Stephens,
1831, which was changed in right form Aphelocnemia in the erratum to the
original publication (according to Villiers, 1978) in 1831: 414; according
to Vives, 2000, in 1832: 406.
#202
Villiers (1970) transfered Mesosa obscuricornis to the subgenus
Perimesosa because of hairy elytrae.
#203
According to Hayashi (1964), Mesosa senilis belongs to the subgenus
Aphelocnemia.
#204
Mesosa hirsuta ssp. continentalis Hayashi 1964 was described from
Korea and continental Russia.
#205
Apriona rugicollis (=germari) was recorded for East Siberia by
Breuning (1962). The occurrence of the species in the region seems to be
possible, because of its very large area (Indie, China, Korea, S-E Asia).
#206
According to J.Vorisek's opinion of 1992, Monochamus saltuarius must
be divided in European and Siberian subspecies.
#207
M. galloprovincialis consists of a number of subspecies: Caucasian
M.g. ssp. Lignator is characterized by strong development of orange-yellow
elytral pubescence, Siberian M.g. ssp. cinerascens just contrary often has
glabrous or nearly glabrous elytra. North of European Russia is already
occupied by very typical M.g.cinerascens.
#208
The spelling of several names in some modern publications: M.
urussovii, Tetrops starkii, Agapanthia dahlii, but second "i" can be
eliminated, because of generally accepted usual spelling with one "i" -
Article 33.3.1 of ICZN (1999).
#209
Siberian M. sutor can be regarded as a separate subspecies M.s.
pellio Germ. 1818 becouse of poor elytral pubescence.
#210
According to E.Vives (2000: 659) Carinatodorcadion is a junior
synonym of Dorcadodium Gistel, 1856.
#211
The subspecies structure of D. carinatum was revised by Danilevsky
(1998b).
D. carinatum from Nizhnii Unal (male, North Osetia, Skalistyi Ridge,
2-5.7.1997, M.Nabozhenko leg. in D.Kasatkin coll.) can be preliminary
attributed to D.c. sunzhenum (from Sunzhensky Ridge).
#212
D. koenigi Jak., described from Daghestan (Temir-Klan-Choura), is
distributed in mountain Daghestan and characterized by narrow body (the
types were studied by me).
#213
The nature of D. caucasicum is not clear (types are not available).
Most probably two closely related populations from near Tbilisi (with
pubescent and with glabrous elytrae) were described as D. caucasicum and
D.sulcipenne. Anyway most of D. caucasicum from Caucasus in
Plavilstshikov's collection are represented by D. sulcipene exertum.
I preliminary accept the traditional interpretation of D. caucasicum
(Plavilstshikov, 1958; Breuning, 1962) as D. cinerarium. Caucasian D.
cinerarium (D.c.caucasicum) are all very different, but in general in this
subspecies autochromal females are less pronounced and sometimes absent
(according to the materials of D.Kasatkin: Karatchaevo-Tcherkessia, Daut
Ravine, 6.1993 and neighbour Uchkulan Ravine 22.6.98 - males with a little
pubescent elytra). The specimens from Teberda in S.Kadlec collection are
glabrous with very rough pronotum.
In Sisian environs and in Karabakh populations both forms of females
are represented. One androchromal (glabrous) female (Megri reg.,
Shvanidzor env., Burtinkar Mt., 24.4.98 Agababian leg.) and one
autochromal (with pubescent elytra) female (Lalvar, 8.6.60) are preserved
in M.Kalashian's collection. His autochromal female from Shorzha
(Gegarkuni reg., 20-25.5.99, M.Nabozhenko leg.) is most probable
D.s.goektshanum.
The taxon described by me as D. cinerarium danczenkoi from Talysh Mts
(Mistan env.) is very special with very rough pronotal sculpture and total
absence of pubescent forms must be better regarded as a species.
#214
Dorcadion panticapaeum was wrongly spelled (as "panticapeum") by
Lobanov et al.(1982).
#215
According to Danilevsky (1992) D. kalashiani sp.n. was recorded
before for Talysh (Lobanov et al., 1981: 789) as D. kasikoporanum. The
latter is known from Arai-Ler Mt. in Armenian Republic.
D. czegodaevi sp.n. was recorded before for Soviet Azerbaidzhan
(Plavilstshikov, 1958) as D. kagyzmanicum Suvorov, 1915; the latter is
absent on the territory of the former USSR.
#216
D. impressicorne was described from Gori; same taxon was later
described as D. sulcipenne exertum. The opinion of Breuning (1962):
impesseicorne = argonauta - is not far from the reality, as D. argonauta
is very close to D. sulcipenne and can be regarded as one of its
Transcaucasian subspecies. D. s. goktshanum Suvorov, 1915 is a well
definite subspecies from Sevan lake environs (I've got a big series from
Sevan city environs).
#217
Dorcadion caspiense Breuning, 1956 was described from Liryk and
regarded as a species (Breuning, 1962). It was regarded by Danilevsky and
Miroshnikov (1985) as D. sulcipenne caspiense. A big series of the taxon
was collected near Lerik in Talysh by A.Nekrasov in 1981.
#218
D. sericatum is regarded here as a species, so D. arenarium was
absent in the USSR.
#219
D. litigiosum otshakovi Suv. was described from near Kherson and
regarded by Breuning (1962) also as a subspecies. According to
Plavilstshikov (1958) D.litigiosum = D. otshakovi. I did not see the
types, but I am sure that the description was connected with very numerous
in the region D. pusilum. D. pusillum is very common all over Ukraine, and
was described from Podolia (Vinitza and Khmelnitzky Regions). I do not
know specimens of D. pusillum from Podolia, so possibly they could differ
considerably from south Ukraine specimens. If so, D. pusillum otshakovi is
a subspecies. But now I prefer to regard D. pusillum = D. otshakovi.
I preliminary regard D. pusillum var. berladense Pic., 1903,
described from Roumania as a subspecies.
It seems that Suvorov's data were the only record of D. litigiosum
(described from Roumania) for Russia. I've never seen D. litigiosum from
the territory of the USSR, so its presence in Ukraine or Moldavia is
rather doubtful.
#220
D. mokrzeckii Jak. was primery found in Crimea out of the type
locality: "Ottuk Mt., 16.4.1999, Andreeva leg." - a pair of not quite
typical specimens in my collection received from V.Dolin.
#221
I've seen in Paris a series, identified by Breuning as D. elegans m.
crimeense Breun. It was D. mokrzeckii. So I regard D.crimeense as a
synonym of D.mokrzeckii and D. elegans most probably absent in Crimea.
#222
Dorcadion elegans was missed in the Key for Caucasus by Danilevsky
and Miroshnikov (1985) though it is known from the region (east
Ciscaucasia).
The species is known westwards as far as Dnepropetrovsk in Ukraine,
where it is very common.
D. elegans is widely distributed in Asian part of Orenburg Region
(Sol-Iletzk Distr., Ak-Bulak Distr.).
#223
According to Danilevsky (1992a) only one Dorcadion species is
distributed in Kopet-Dag, though the synonymy D.tuerki = D. komarowi was
wrong. According to my series from Mazanderan (where the type locality -
Hadschgabad - is situated), D. tuerki is in general bigger with less
developed (or absent) erect elytral setae. But D.tuerki was absent in
USSR.
D. komarowi is not a synonym of D. kryzhanovskii. The latter is
characterized by black legs and antennae with numerous black spots on
elytral white stripes, while D. komarowi has usually red legs and antennae
with rare or absent black elytral spots. So D. k. kryzhanovskii is a
subspecies from Germab valley.
#224
According to my study of the syntypes: Dorcadion euxinum Suvorov,
1915 = D. kubanicum Plav. 1934, that agrees with Plavilstshikov's (1958:
181) description of the type of D.euxinum. According to Plavilstshikov
(1958) a part of D. euxinum syntypes were D. cinerarium.
In fact the difference between D. sareptanum and D. euxinum is very
small and sometimes totally absent. Several populations of D. euxinum are
with very dark antennae and legs that is unknowm in D. sareptanum (black
legs and antennae was the main reason for D. kubanicum), but D. euxinum
with red legs and abtennae are also known, so I prefer to regard it as a
subspecies.
The type (male) of D. striatiforme is in very bad condition. I was
not able to identify it good enough. It can be very small D. holosericeum
or D. sareptanum euxinum. Both species are rather common in the region.
#225
D. tristriatum is connected by the row of transitional forms with D.
holosericeum, so I regard D.h. tristriatum as south subspeciers. It is
distributed eastwards along Caucasian Ridge to Daghestan - one male from
near Tlokh (2000m) in Andiyskoe Koysu Valley (27.5.1988, V. Karasev leg.,
collection of S. Saluk).
#226
D. equestre m. transsilvanicum Ganglb., 1884 was described from
Serbia and South Romania, so this subspecies can be represented in
Moldova.
#227
According to Danilevsky and Khvylia (1997), Dorcadion shirvanicum
Bog. 1934 = D. azerbajdzhanicum Plav. 1937
#228
D. bisignatum was recorded by Breuning (1962) for Batumi and regared
by Plavilstshikov (1958) as very possible for Adzharia.
#229
According to the original description, D. indutum had to be described
from east Transcaucasie, most probable from Karabakh. Just here the forms
(and in Garni district of Armenia) with pale elytral stripes are
distributed. Black forms, described as nigrosuturatum, are distributed
north-westwards Sevan Lake. D. griseipenne was also describe from here
(Semenovka).
#230
Dorcadion sodale Hampe was recorded for USSR (Abbastuman, Achalzich)
by Breuning (1962).
#231
According to Danilevsky (1992a), D. jacobsoni = sokolowi = conicolle;
and according to Danilevsky (1993b), D. jacobsoni = apicipenne = sokolowi
= amymon = dsungaricum = melancholicum = conicolle and possibly =
merzbacheri.
I do not know the type of D. merzbacheri. Its type locality is
uncertain - "Thian-Shan". But in the original description it was compared
with "D. lucae" sensu Breuning, so with D. jacobsoni and could be
conspecific to it.
D. obtusicolle is a good speceis (I've studied the type in Prague),
that agree with Plavilstshikov's (1958) opinion, and just contrary to
Breuning's (1962) opinion.
#232
D. samarkandiae was described after one female from "Samarkand"
environs and was compared with "D.lucae" sensu Breuning (that meens - D.
jacobsoni). Only one species can be in this region - D. turkestanicum, and
its females can be really similar to D. jacobsoni, but if the locality was
wrong, it must be D. jacobsoni.
#233
According to Danilevsky (1993b): Dorcadion musarti Pic, 1907 is very
close to D. morozovi, but is a separate species.
#234
D. morozovi was found in China in the east part of Ketmen Ridge on
Sarybutchun Pass (northwards Tekes-city): 1 male, 2300m, 11.6.99,
I.Belousov leg. (my collection). It was collected together with several
very big D. rufogenum.
#235
The revision of subspecies structure of D. semenovi was published by
Danilevsky (2002a). Old distributional data on D.s. semenovi and D.s.
hauseri published by me (Danilevsky, 1993b) were revised.
#236
Old data on the occurence of D. kuldshanum in Przhevalsk environs
(Plavilstshikov, 1958; Breuning, 1962; Danilevsky, 1993b) were most
probably based on specimens fron China territory. No reliable data on the
occurence od the species in Kirgizia (or in Kuldzha environs) were
available (Danilevsky, 2002a).
#237
New locality (about 160km eastwards Narynkol along Tekes River
Valley) of Dorcadion kuldschanum in China at the western most part of
Narat Ridge in Koksu River Valley south-eastwards Tekes (several males,
2000-2300m, 12.6.1999, I.Belousov leg.) makes more possible the occurrence
of the species in Kazakhstan near Narynkol.
#238
According to Danilevsky (1996a), D. politum = D. lydiae. The types of
D. lydiae (from Semipalatinsk) are just the most colourful specimens from
the series, which was the base for D. politum ab. nanellum - small D.
politum politum.
I.A. Kostin (1973) proposed another synonyms D. eurygyne =
balchashense = lydiae, that was absolutely wrong.
The occurrence of Dorcadion politum in European Russia was
supposed by me (Althoff, Danilevsky, 1997) on the base of a single
male with a label: "Orenburg, 30.4.1963". Now the occurrence of D.
politum in Orenburg Region is proven by a series from the Asian
part of Orenburg Region (5 males: Sol-Iletsk District, 25km
southwards Pokrovka, 24-27.5.2002, L.Korshikov leg.). My
supposition of the species for European part of Kazakhstan was
evidently wrong.
#239
The separation of Compsodorcadion and Dorcadion s.str. was published
by Danilevsky (1996a).
#240
According to Danilevsky (1992a), D. crassipes is the valid name for
D. obtusipenne sensu Plavilstshikov (1958), Breuning (1962) and others
(not Motschulsky, 1860). D. obtusipenne was described from Kzyl-Orda
environs and could be regarded as a valid name for D. androsovi as was
proposed by Danilevsky (1992a), but better both taxa must be regarded as
subspecies: D. glycyrrhizae androsovi and D. g. obtusipenne (according to
Danilevsky, 2001a).
The subspecific structure of D.crassipes was published by Danilevsky
(1996a).
#241
Dorcadion ganglbaueri up to now is known only from Kazakhstan and the
record for Central Asian republics by Lobanov et al. (1982) was a mistake.
According to Plavilstshikov (1958) it is distributed between Tchimkent and
Vysokoe. I also know a good series from Aksu-Dzhabagly (Ak-Su River
Valley, 2000m, 21.5.90, A.Konstaninov leg.). A new unusual locality of
this very rare species was found by me in Central Karatau Ridge near
Zhanatas (several hundreds of specimens on 27.4.93).
#242
The subspecies structure of D. gebleri was revised by Danilevsky
(1996e).
D. gebleri is the longest known Dorcadion (30.0mm - male in my
collection; females are shorter, but wider). The biggest known
Dorcadionini is Eodorcadion heros Jakovlev, 1899 from Mongolia (males - up
to 25.0mm, females - up to 32mm; both in my collection).
#243
D. gebleri n. occidentale, raised to subspecies by Breuning (1962),
was described from "Kirgisensteppe westwarts bis zur Wolga". The locality
is impossible for D. gebleri known from east Kazakhstan. I saw the type in
one of private collections. It was really normal D. gebleri, as it was
published by Plavilstshikov (1958). So the type locality was wrong.
#244
A population of Dorcadion glycyrrhizae striatum (= rufifrons) from
Orsk environs (1 female - Orenburg Region, Guberli, 2.6.98, O. Gorbunov
leg. and a series from same locality, 1-5.5.2001, M.Smirnov leg. - all in
my collection) is characterized by a big number of specimens with totally
black antennae and totally black femora. Such specimens are mixed with
specimens of normal colour (red basal antennal joints and red femora).
#245
The subspecies structure of D. glycyrrhizae was revised by Danilevsky
(2001a).
The occurrence of D. glycyrrhizae glycyrrhizae in Russia is
rather doubtful. From Volgograd environs to Kazakhstan border and
northwards to Saratov Region D. g. striatum is distributed (so
Plavilstshikov's data for Saratov and Orenburg Regions were sure
wrong). Russian D. g. glycyrrhizae can occur only in Astrakhan
Region in sands eastwards Volga.
The type locality of D. g. striatum is "South Urals". In fact
several rather different populations of D. glycyrrhizae
(includindg D.g.dubianskii) are known from South Urals. I accepted
as typical the population from the southmost point of Orenburg
Region from the valley of Shybyndy River (15 males and 4 females:
Sol-Iletsk District, 25km southwards Pokrovka, 24-27.5.2002,
L.Korshikov leg.). It consists of rather big specimens with
totally red tibiae, femora and several basal antennal joints;
frons is also usually red; female androchromal. Such specimens are
very close to D.g. striatum from Saratov and Volgograd Regions
(with neihbour localities in Kazakhstan: Dzhanybek env.).
I preliminary attribute to D. g. striatum several populations
of small beetles from middle part of Ural River Valley (right
European bank) in Kazakhstan (eastwards Ural-city in Bykovka River
Valley and Ianvartzevo env.) and near Kalinovka (about 120km
westwards Aktiubinsk).
#246
The synonymy: D. cephalotes = turgaicum by Kostin (1973), who
followed Plavilstshikov's (1958) opinion on close relations between two
species, was accepted by Tsherepanov (1983). In fact two species belong to
different subgenera. Very rare D. turgaicum was unknown for Kostin and
Tsherepanov. I've collected many specimens near Esil (Astana Region)in two
seasons: 18.5.1992 and 1.5.2001.
Two new localities of D. turgaicum: "Astana, Khan-Tau 6.74, V.Skopin
leg." - 1 male in my collection; "Atbasar env., 5.74, V.Skopin leg." -
male and female in my collection.
#247
The subspecies structure of D. arietinum was revised by Danilevsky
(1996d). According to Danilevsky (1996d), D. lucae Pic, 1898 (the holotype
female is in Eberswalde), described from Kuldzha is a subspecies - D.
arietinum lucae, known up to now oly from Kuldzha (Yining). Ealier it was
regarded by Danilevsky (1992a)as a valid species name for D. strandi.
Breuning (1962) wrongly interpreted D.lucae as a valid name for
D.apicipenne = sokolovi. For Plavilstshikov (1958) D. lucae is a separate
species close to D. strandi.
#248
The subspecies structure of D. suvorovi was revised by Danilevsky
(1996b).
#249
D. suvorovianum was restored by Danilevsky (1999d).
#250
D. matthiesini(sic!) m. unidiscale Breuning, 1946 (from Almaty) was
regarded as D. globithorax ssp. uniduscale by Danilevsky (1996a)from
Kaskelen Ravine and then (Danilevsky, 1999d) as a species D. unidiscale.
#251
The subspecies structure of D. mystacinum Ballion, 1878 is not
investigated yet. The taxon was described from "Kuldzha". Though the name
was traditionally attributed by all authors to the species from near Aulie-
Ata (= Dzhambul = Taraz). I don't know the type, but most probably the
Ballion's specimens were really collected near Aulie-Ata. It was very
usual for Ballion to mention "Kuldzha" as type locality for the species
from Kazakhstan (for example Carabus lindemanni Ballion, 1878).
D. rufidens was described from "Syr-Daria" - the type is in S.-
Petersburg with label: "Syr-Darja, Arys". It meened the nearest to Arys
slopes of Karatau Ridge as the species close to D. mystacinum is not known
from the plane between Karatau and Syr-Daria. So I regard under the name
D. mystacinum rufidens all mountain populations of D. mystacinum from
Karatau. According to available materials, D. mystacinum from different
parts of Karatau are very different and further subspecies divisions are
desirable.
D. pumilio, described from near Chu-city is connected with
D.mystacinum by a row of transitional populations.
The combinations D. mystacinum rufidens and D. mystacinum pumilio
were published by Danilevsky (1999d: 39). Both taxa absent in Kirgizia.
The record for Central Asian republics by Lobanov et al. (1982) for D.
pumilio were based on the data from original description for "Frunze
environs", which were really concerned with D. optatum matthieseni;
another original record for Alma-Ata environs were also wrong. The wrong
record for Central Asian republics by Lobanov et al. (1982) for D.
rufidens were based on Plavilstshikov's (1958) data, that the area of
D.rufidens is totally same that of D. mystacinum.
#252
The subspecies structure of D. optatum was revised by Danilevsky
(1999d).
#253
The subspecies structure of D. tianshanskii was revised by Danilevsky
(1999d).
Breuning (1962) used wrong spelling of radkevitshi ("radkewitschi").
#254
I've studied twy syntypes (males) of Dorcadion globithorax var.
alexandris Pic from "Alai" (a female from same series belongs to another
pecuies) in Paris. The taxon was later described as D. luteolum, as it was
published by Plavilstshikov (1958).
#255
According to Danilevsky (1999d), D. globithorax, described from near
Kapchagai, is known up to now only from the type locality. Numerous
records of this species from other regions belong to other species.
#256
After study a big series of D. tibiale toropovi, collected by me
(7.5.2000) in itstype locality, I see that it must be considered as a
species.
#257
The real area of D. pelidnum (the environs of Bystrovka = Kemin only)
was described by Danlevsky (1999d).
#258
Iberodorcadion fuliginator was recorded for Lithuania (Telnov et al.,
1997), so - D.f.fuliginator.
#259
I do not see the declared differences between Eodorcadion s.str. and
Ornatodorcadion.
#260
E. carinatum was described ater one specimen from "Siberia". I do not
know the type and regard as typical the populations of the species from
West Siberia (Russian regions: Orenburg, Cheliabinsk, Kurgan, Omsk,
Novosibirsk; Kazakhstan regions: Kustanai, Kokchetav, Atbasar,
Semipalatinsk. I've got a pair of E.c.carinatum from Cheliabinsk Region.
E. altaicum was described from Narym River Valley (right tributary of
Irtysh southwards Zyrianovsk: Bolshenarymskaia, Altaiskaia). It is very
special form, not a synonym of the nominative. I've studied the syntypes.
According to the original description of E. involvens m. blessigi, is
a common Altai form of E. carinatum with irregular white elytral stripes
distributed in Shebalino environs and southwards Chemal, and probably
(according to Suvorov, 1909) as far eastwards as Minusinsk.
Chemal environs are occupied by E. carinatum with regular white
elytral stripes - E.c. bramsoni (= gassneri). I've studied the holotype of
Neodorcadion carinatum v. bramsoni in Budapest.
#261
Eodorcadion dorcas was recorded fo Russia (Plavilstshikov, 1958), but
most probably it absent in Russian fauna, as its area is very far from
Russian border (see Namhaidorzh, 1972). Plavilstshikov's (1958) data on E.
dorcas area looks fantastic. It could be easy missed with other black
species.
The presence in Tuva E. humerale impluviatum seems to be possible but
rather unlikely.
#262
"Black" Eodorcadion of Tuva are represented by 3 close allopatric
taxa, which could be regarded as species or subspecies:
E. ptyalopleurum, described from Barlyk River, is distributed
eastwards up to Chadan only. It is also known from Shui River in the
environs of Teeli and Ak-Dovurak. The taxon is characterized by rough
elytral sculpture with several granules on shoulders, with bright white
apical elytral stripes, with dense white abdominal pubescence.
The type locality of E. maurum (Àëòàé) was wrong. According to
Namhaidorzh (1972) the type series was collected near Ulangom. Same
populaion was partly used for the description of E. grumi. Another part of
D. grumi syntypes was collected in north Tannu-Ola (I've got such
specimens from Torgalyk River and in collection of S. Kadlec a big series
from Khadyn Lake is preserved). I do not see the difference between
specimens from Tuva and Mongolia. If the diference exists, the synonymy
maurum=grumi could be canceled, after respective lectotype designation.
Now the area of the taxon is very large. Tuva: planes northwards Tannu-
Ola, hills southwards Tannu-Ola from Mugur-Aksy to Samagaltai. Mongolia:
west part of Greate Lakes Valley southwards up to Kobdo. It is
characterized by smooth, often shining elytra without humeri granules,
without epical elytral white stripe, abdomen with less dense pubescence.
E. tuvense: most part o the type series was collected near Chaa-Hol,
but holotype is from Chadan environs. The taxon is also known from
Shagonar environs. The environs of Ishtii-Hem and Khondergei River Valley
(a part of type series) are occupied by transitional populations (to
E.ptyalopleurum). The taxon is characterized by dull elytra without
humeral granules and without apical stripes; elytra always with very
special white sparce pubescence.
In all three taxa forms with regular white elytral stripes or with
deep longitudinal furrows are known.
#263
According to Namhaidorzh (1972), E. carinatum involvens m.
bicoloratum Plavilstshikov, 1958 is in fact a form of E. lutshniki without
white stripes (I saw syntypes in Plavilstshokov's collection, Moscow).
According to my materials this form has very distinct area and so must be
regarded as subspecies. I know 3 populations: Shurmak environs (east Tannu-
Ola), Erzin environs (Saluk collection, Minsk) and according to
Namhaidorzh (1972)- Tes environs in Mongolia. In Tes population striated
and glabrous specimens are mixed - all with special sculpture and body
form, so could be separated in new subspecies (ZIN collection, St.-
Petersburg).
#264
Eodorcadion katharinae Rtt., described from north Mongolia (most
probably from Ubsu-Nur Lake Valley) after one male (holotype in ZIN,
St.Petersburg) and represented in my collection by three males (south,
east and north of the lake) must be evidently excluded from Russian fauna
as Russian forms from Tere-Hol Lake and Erzin environs taransitional to
typical E. quinquevittatum (south Kyzyl environs) are much more closer to
E. quinquevittatum than to E. katharinae. Both forms must be regarded as
subspecies.
E. leucogrammum Suv., described from north Tannu-Ola (in my materials
typical population is represented by specimens from Bai-Haak) is also
connected with E. quinquevittatum by a row of transitional populations and
is in fact its subspecies. E. leucogrammum is also known to me from the
north Kyzyl environs (2 males with very distinct longitudinal furrows from
Siserlig: 20.6.97, V.Patrikeev leg., in D.Kasatkin coll.; a series from
Sush: 15.6.97, S.Vaschenko leg.) up to Turan and to the east up to Saryg-
Sep.
E.q.quinquevittatum is known to me eastwards up to Ishtii-Hem, but
must be distributed at least up to Chadan.
#265
Now I accept Cerambyx hispidulus Piller et Mitterpacher, 1783 as type
species of Pogonocherus Dejean, 1821 following the opinion of P.Svacha
(2003, personal communication):
Genus Pogonocherus Dejean, 1821
Type species: Cerambyx hispidus F., 1775 (nec L. 1758) = Cerambyx
hispidulus Piller & Mitterpacher, 1783 (Guerin design., 1826).
#Dejean_fs 1821 catalogue contains _ghispidus_h without any
author_fs name, but, according to J.A. Chemsak (pers. comm.),
Dejean in later editions of his work (not seen by me) attributed
the name to Fabricius. Also other indirect indications, such as
selection and ordering of species names or mentioning
_g(Cerambyx. Fabr.)_h under the generic name Pogonocherus,
suggest that Dejean used the classification of Fabricius. There
is unfortunately no material of Fabricius_f Cerambyx hispidus in
his collection in the Zoological Museum in Copenhagen (O. Martin,
pers. comm.), but hispidus sensu Fabricius was undoubtedly
misidentified. Characterizing Cerambyx hispidus, #Fabricius
(1775) obviously had before him Pogonocherus hispidulus since he
clearly mentioned bidentate elytral apex (_gCerambyx thorace
spinoso, elytris apice bidentatis, antennis mediocribus
hirtis_h), although he considered his specimen(s) identical to
the Linnaean species (he also cited the Linnaeus_f 1758
description of Cerambyx hispidus from Systema Naturae, but that
description does not mention shape of elytral apex). #Fabricius
(1787) repeated his earlier characteristics of C. hispidus and
described Cerambyx pilosus which is probably the true Linnaean
hispidus (unidentate elytral apex). The name pilosus (again
without author_fs name) was also included by Dejean. I therefore
accept the approach of #Linsley & Chemsak (1985) and regard
Pogonocherus hispidulus (Piller & Mitterpacher, 1783) as the type
species of Pogonocherus Dejean, 1821.
#266
According to Lobanov et al. (1981), Pogonocherus dimidiatus =
tristiculus. The synonymy was accepted by G.O. Krivolutzkaia (in:
Tsherepanov, 1996).
According to Gressitt (1951), P. dimidiatus Bl., 1973 = P. seminiveus
Bates, 1873. Both names were accepted by Tcherepanov as the names of
different species (island and continental). I do not see the differences
between both populations, so traditional synonymysation is right.
The dates of both names must be checked: according to Kusama and
Takakuwa (1984) and Ohbayashi, Sato et Kojima (1992): seminiveus
Bates,1873 = dimidiatus Bl.,1873.
#267
According to Dzhavelidze and Danilevsky (1981), Pogonocherus
caucasicus = P. kuksíà. According to Danilevsky and Miroshnikov (1985), P.
sieversi = P.caucasicus = P.kuksha.
#268
According to A.F. Bartenev's materials collected in Crimea from Pinus
and identified by A.Lobanov in 1982, Pogonocherus perroudi presents in
Crimea.
According to P.Svacha (personal communication, 2002) larvae of P.
perroudi from Pitsunda (Georgia, Caucasus) were collected by J. Kratochvil
from Pinus in 1987 and adults were reared.
#269
According to E.Vives (2000), the date of Pityphilus Mulsant is 1862.
#270
P. costatus (described from Jakutsk) was often regarded as dark
Siberian (including Japan) subspecies of P. fasciculatus (Breuning, 1963,
1975; Kusama and Takakuwa, 1984). But similarly colored specimens are also
known even in Europe (Breuning, 1963), as well as in Siberea pale
specimens are also common (my materials). Pogonocherus fasciculatus =
P.costatus (see Danilevsky, 1998a).
Tsherepanov (1984) regarded both as different species with distinct
larval characters. Caudal larval plates of Tsherapnov's "costatus" from
Tomsk environs are impossible for P. fasciculatus. The picture of imago is
also very special, so identification of his species rests unclear. It is
necessary to try to look for these specimens in Novosibirsk.
According to P.Svacha (personal communication of 2002), who studied
the larvae of "P. costatus" from Tsherapanov's collection, most probably
it is P. decoratus. So, P. decoratus is distributed eastwards at least to
Altai Region.
#271
Oligoenoplus rosti iwatai Ikeda, 1987 was described from Japan.
#272
According to E.Vives, Pogonocherus ovatus Goeze, 1777 was described
as Cerambyx (not Sulzer, 1776) and must be replaced by Pogonocherus ovalis
(Gmelin, 1790). The change can not be accepted according to the Article
23.9. of ICZN (1999)
#273
According to E.Vives (2000), Aegomorphus clavipes (Schrank, 1781)
was described as Cerambyx (not Forster, 1771) and must be replaced to A.
varius (F., 1787). The change can not be accepted according to the Article
23.9. of ICZN (1999).
#274
According to Sama (1995), Oplosia fennica (Paykull,1800), described
as Lamia fennica (nec Linnaeus, 1758) must be replaced with Oplosia
cinerea (Mulsant, 1839).
#275
According to Miroshnikov (1990) Acanthocinus giseus in Caucasus
region is known from N Caucasus (Ubinskaia, Gelendzhik) and from Armenia
(Arzakan, Idzhevan).
#276
According to Hasegawa (1996) Acanthocinus griseus orientalis is a
species as well as A. carinulatus sachalinensis.
So, Kunashir (2 males and 3 females in my collection) and possibly
Iturup (Krivolutzkaia, 1973) are occupied by A. orientalis, which is also
distributed in Japan (Hokkaido, Honshu, Shikoku, Kiushu, Tsushima,
Yakushima).
According to Hasegawa (1996), A. sachalinensis is distributed in
Sakhalin, Hokkaido, Russian Primorie, Korea and in North China. But my big
series from Primorie, Amur Land, Chabarovsk and Magadan Regions mostly
consist of typical A. carinlatus, though include several specimens, which
look not so typical.
A. carinulatus was recorded by Hasegawa from Altai to Buriatia only.
According to Hasegawa (1996), A.griseus is totally absent in Siberia,
though there are some very typical specimens of A. griseus in my
collection from Tomsk and from Krasnoiarsk.
In general the situation with Acanthocinus species in Siberia rests
unclear.
#277
According to J.Voricek (personal communication of 1992), Leiopus
caucasicus must be regarded as a species, which is closer to L.bedeli,
than to L.nebulosus.
#278
According to Breuning (1978), Leiopus femoratus = L. pachymerus.
#279
According to Breuning (1978), Lobanov et al. (1981,1982) and
Tsherepanov (1984) Leiopus malaisei (described from Kamtchatka)is a
species. According to Ivliev, Kononov (1966) it is just L.albivittis m.
malaisei from Magadan environs. According to Danilevsky (1988a), it is L.
a. ssp. malaisei.
#280
According to Baeckmann (1924), Leiopus albivittis = L. ganglbaueri
(described from Enisei river southwards Krasnoiarsk); Pseudopidonia
alticolluis = tristicula; Chloridolum sieversi = Aromia coreana.
#281
According to Teocchi (1983), E. adspersus = E. alem-daghensis Breun.
#282
Exocentrus hirsutulus (Fald.,1837) was recorded for Caucasus on the
base of 2 specimens collected in Nakhichevan by S.M.Iablokov-Khnzorian
(Lobanov et al., 1982; Danilevsky and Miroshnikov, 1985). Plavilstshikov
(1927) proposed to regard the name as nomen nudum, because of poor
description. The species was excluded from the genus revision by Breuning
(1958). We accept here the position by Winkler (1929) E. adspersus = ?
hirsutulus.
Specimens from Nakhichevan most probably represent a new species.
#283
According to J.Vorisek (personal communication of 1992) Ex.
punctipennis from Transcaucasie can be attributed to E. punctipennis
signatus, described from Konstantinopol and recorded for Turkey and Greece
(Breuning, 1958).
E. punctipennis was recorded for Rostov Region by Kasatkin and
Arzanov (1997), then for Rostov Region, Minsk and Kiev by D.Kasatkin
(1998).
#284
A.I.Tsherepanov (1985):
transferred Eumecocera to Saperdini on the base of larval characters;
recorded Oberea scutellaroides for Russia (as O. chinensis sp.n.);
regarded Molorchus semenovi as a subspecies of M. kiesenwetteri Muls.
#285
According to Danilevsky (1988d), Stenostola atra Gressitt, 1951 was
recorded for Russia (Lobanov et al.,1981,1982) on the base of wrong
determination of Eumecocera callosicollis.
#286
E.Vives (2000) regards Cerambyx carcharias L., 1758 as type species
of Saperda (Westwood designation, 1840), while in fact it is Cerambyx
scalaris L., 1758 (Curtis designation, 1829). So, Anaerea is not a synonym
of Saperda.
There is no type designation of Saperda in "Hist. Nat. Gen.et Partie"
Tome 3 by Latreille (1802: 215) as it was stated by some colleagues.
Latreille's text: "Les saperdes de Fabricius. Exemple Saperda carcharias
F." - is not a type designation.
I prefer now to regard Saperda s.l. consisting of several subgenera
including Lopezcolonia (replacing name for Argalia Mulsant, 1862 not Gray,
1846).
#287
According to Danilevsky (1993b):
Saperda subobliterata = S. mandschukuoensis = A. harbinensis (the
last position was originally published by P. Dessart (1983).
Conizonia (Iranocoptosia) fausti = I. balashowskyi.
#288
One female from Khabarovsk Region (10-17.7.1991, Shadinkov leg.) was
preliminary identified by me as Saperda bilineatocollis Pic. It is close
to S.populnea, but without elytral spots and with bright pronotal hair
stripes.
#289
According to Danilevsky and Miroshnikov, 1985, Stenostola
maculipennis is a subspecies of S.ferrea.
#290
Nupserha alexandrovi must be included in Japan fauna (Tokio env.,
24.7.32 and 27.7.38, N.Filippov leg. - male and female in my collection).
The date of N. alexandrovi was wronly mentioned by Lobanov et al.
(1982) as 1921. Many original Plavilstshikov's descriptions of 1915 were
published once more in 17th(1917) volum of Russ.Ent.Obozr. appeared in
1921. That is why wrong "1921" appeared in many publications (Gressitt,
Breuning) for: Macrorhabdium, M. ruficolle, Gaurotes kozhevnikovi,
Pseudopidonia unifasciata, P. subsuturalis, Ropalopus speciosus.
#291
The synonymy Oberea herzi = coreana, accepted by Lobanov et al.
(1981) and Tsherepanov (1985) was wrong, and our reference to Breuning
(1960-62) was not exact, as Breuning proposed another synonymy: O.herzi =
morio = scutellaroides = coreana. According to Gressitt (1951), all four
are different species. Here I regard O. morio = coreana and others names
belong to different species.
#292
Oxilia argentata was recorded for Iran (Tegeran) by Breuning
(1967)and for Crimea by Bartenev (1989).
#293
Pteromallosia albolineata was regarded as Conizonia (Pteromallosia)
albolineata by Breuning (1954) or as Conizonia albolineata by Lobanov et
al. (1982).
#294
According to Danilevsky (1990), M. scovitzi tristis Reitter, 1888 =
M. angelicae Rtt., 1890.
A population of Mallosia from Armenia northwards Bichenek Pass
(Angechakot, 1600m, 20.6.87, Kadlec et Vorisek leg. - one male in my
collection) is morphologically identical to typical M. tristis from
Talysh. Taking into account that typical M. scovitzi is very common
southwards Bichenek Pass and all around Armenia, I prefer to regard M.
tristis as a species.
#295
Paramallosia afghanica Fuchs was found in Turkmenia: one specimen
from Kopet-Dag (without exact data) in collection of S.Murzin and one
female (Kopet-Dag, Ipai-Kala, 6.5.1989) in my collection.
#296
Phytoecia kubani described from Tadzhikistan must be placed in
Conizonia.
#297
A male of Ph.(Helladia) humeralis and a male of C.(Eurycoptosia)
bodoani (both in my collection) were found by V.Siniaev (1992) in Talysh.
#298
Phytoecia tigrina (Armenia) and Agapanthia maculicornis (Dagestan)
were recorded for Caucasus by Miroshnikov (1990).
According to my observations, A. maculicorinis was rather numerous in
Volgograd Region (June 1999) on Tragopogon (Compositae). The species was
also recorded (Bense, 1995) for Helianthus, and (Kovacs and Hegyessy,
1997) for Campanula glomerata. While very close A. korostelevi develops in
Armenia on Scorzonera pulchra (Compositae).
#299
Conizonia (Coptosia) bithyniensis Ganglb., 1884 was recorded for
Ordubad by Breuning (1954).
Coptosia was regarded as a genus by Plavilstshikov (1948), Bense
(1995).
According to Breuning (1966: 741) it is a subgenus of Conizonia.
According to Lobanov et al. (1981), it is a subgenus of Phytoecia.
#300
According to Danilevsky (1988d), Mallosia imperatrix Dan. was
recorded for USSR fauna (Lobanov et al., 1982) after wrong interpretation
of Plavilstshikov's (1948) record for Armenia M. imperatrix
cribratofasciata Dan., that is just a synonym of M. caucasica Pic
(Breuning, 1954). Mallosia imperatrix absent in Transcaucasie.
#301
According to J.Vorisek (personal communication of 1992) most of
subgenera of Phytoecia s.l. must be regarded as genera. Pseudocoptosia
must be subgenus of Conizonia, and Pseudomusaria must be a subgenuas of
Musaria.
#302
I regard: Ph. cinerascens Kr., 1882 = Phytoecia sokolovi Sem., 1895
and Ph. eylandti Sem., 1891 = Phytoecia glasunovi Sem., 1895.
#303
I (1994) identified in Dubatolov's (Novosibirsk) materials:
1 male of Agapanthia nigriventris (Badkhyz, 20-25km SE Polekhatum,
Gezgiadyk Ridge, 15-16.4.93, D.V. Logunov leg.);
Phytoecia eylandti (Badkhyz);
Dorcadion gebleri (Kemirkol Lake, SW Kurchum, 26.6);
D. eurygyne (left Irtysh bank near Ust-Kamenogorsk, Menovoe, 19.8.88
and Serebriansk env., 7.5.93).
I received 1 male and 2 females of A.nigriventris (Badkhyz,
Gezgiadyk, 10.4.1993, A.Klimenko leg.).
#304
According to Plavilstshikov (1961), Phytoecia farinosa = mucida.
#305
Ph. pretiosa ninives Sama, 1994 was described from Irak.
#306
According to Danilevsky and Kadlec (1990) 3 ex. of Ph. (Helladia)
orbicollis were collected near Biurakan. S.Kadlec accepted (2002) the
opinion of G.Sama and P. Rapuzzi (2000: 20) that Helladia orbicollis is
endemic of Liban. From Turkey to Armenian Republic it is replaced by
Helladia adelpha (Gangl.). According to Rejzek, Sama and Alziar (2001:
279), it is a subspecies H. orbicollis adelpha (Ganglb., 1885), but
according to Sama and Rejzek (2001: 242) it is a separate species Helladia
adelpha (Ganglb., 1884). Now I've accepted here the last position with the
date of original description (1885) from Breuning (1951).
#307
A big series of Ph. iranica in collection of C.Holzschuh (Vienna)
includes specimens with same elytral design as in Ph. armeniaca and as in
Ph. natali; though in Armenia strong development (and fusion) of black
elytral spots is unknown. Ph. natali is up to now (2001)known after only
one specimen (from near Altyagach in Azerbajdzhan). Until new materials
available it would be better to regard all 3 taxa as subspecies.
#308
Ph. rubropunctata was recorded for Czechia and Slovakia by Heyrovsky
(1955), for Crimea by Plavilstshikov (1965) and on the base of this record
by Lobanov et al. (1982) for USSR. According to Bense (1995) all records
of Ph. rubropunctata for East Europe were connected with wrong
determination of Ph. argus. The easten most locality of Ph. rubropunctata
is in West Germany.
#309
Ph. affinis (Europe), tuerki (Brousse, Turkey), boeberi (Teberda) and
volgensis (Volga River) were usually regarded as different species
(Breuning, 1951; Plavilstshikov, 1965; Lobanov et al., 1984). The natural
relations between all four taxa are not clear.
I do not now in Caucasus specimens with so bright orange pubescence
as in certain specimens from Brusse (but other specimens can be very
similar to Caucasian).
All specimens from Volgograd environs are with pale elytral
pubescence and such typical Ph. volgensis can be collected westwards up to
Stavropol, though already from Daghestan they are mixed with specimens
covered by black pubescence and both forms can be here with red or black
pronotum. Even in Teberda the typical Ph. boeberi with black pronotum are
mixed with specimens of red pronotum, which are very close to European Ph.
affinis (Ph. affinis from Europe also can be sometimes with black pronotum
as well as with pale elytral pubescence).
Specimens with black pronotum are dominant in Armenia, Azerbaidzhan
(including Nakhichevan), East Georgia (Tbilisi and eastwards) and seems in
north Caucasus from Daghestan to Stavropol.
Specimens with red pronotum are dominant in West Caucasus including
West Georgia (Borzhomi), Black Sea Coast, Krasnodar environs and mountains
around Guseriple.
So I prefer now to regard all four taxa as subspecies.
Ph. a. nigropubescens is a preliminary name for Caucasian subspecies
with red pronotum specimens dominating. I do not know the type locality of
this name - if it is Teberda, then boeberi = nigropubescens, and for West
Caucasian subspecies must be found another name (circassica Rtt., 1888;
starcki Rtt., 1888).
The combinations Ph. nigripes ssp. nigropubescens and Ph. nigripes
ssp. tuerki were published by Villiers (1978).
#310
Ph. astarte lederi, distributed in Transcaucasie, differs from the
nominative subspecies from Turkey by black elytral pubescence.
#311
Ph. puncticollis stygia Ganglb., 1886 from Kopet-Dag is always with
black prothorax.
#312
According to Breuning (1951) the author of Ph. (Neomusaria) suvorovi
is not Koenig, 1906 (Plavilstshikov, 1930, 1948), but Pic, 1905.
The species was recorded for Caucasus by Lobanov et al., (1982) and
for Armenia (Megri) by Danilevsky, Miroshnikov (1985), both records were
without exact data. One mail was collected in sands near Goravan by
M.Kalashian (May, 2001).
#313
Ph. analis Mannerheim, 1849, not Ph. analis (F.,1781), was changed by
Breuning (1951) to Ph. mannerheimi. I do not know, why another names
(ferrea Ganglbauer, 1887; or atropygidialis Pic, 1939)were not used.
#314
According to Lobanov et al. (1981), Ph. pustulata (m. pulla) = Ph.
kryzhanovskii.
According to Danilevsky (1992), Phytoecia pustulata = Ph. pilipennis
(Ordubad).
Ph. pustulata from Kazakhstan and from SE Russia is sometimes without
red pronotal spot, and body is covered with very long and dense white
pubescence. Such specimens (m. pulla) from Kazakhstnan and Uzbekistan
(Karatau Ridge, Chatkal Ridge, Chu-Ili Mts and eastwards to Semipalatinsk)
were described as Ph. kryzhanovskii and must be regarded as Ph. p. ssp.
pulla. The subspecies was accepted by Heyrovsky (1958) for Astrakhan env.
In my collection Ph.p.pulla is represented by a syntype (male) from
Karatau, male from Dzhungarsky Alatau, male from Sary-Chelek (Kirgizia)
and a male from Chechnia (Caucasus). Some Kazakhstan and Kirgizian
populations can not be attributed to Ph.p.pulla, being rather typical
Ph.p.pustulata (Bishkek env., Kalbinsky Ridge).
Also specimens from Caucasus are often darker with veru dense
pubescence and can be regarded as Ph. p. murina.
#315
According to G. Sama (1988a: 184), the records of Ph. rufipes for
Siberia and Central Asia are connected with wrong identification of
another species - Ph. sibirica. Same statemen (Sama, 1988) was explained
by monophagy of Ph. rufipes on Foeniculum, which is absent in Russia and
Central Asia.
After study of my series of Ph. rufipes from Kazakhstan G.Sama
(personal communication) recognized, that it did not differ from European
specimens and must be identified as Ph. rufipes. According to my
observations, Ph. rufipes developes in Kazakhstan and Central Asia on
Prangos spp.
Ph. rufipes latior Pic, 1895 (Akbes, Turkey) was restored by Sama
(1996).
#316
Phytoecia cinctipennis was recorded for Kurgan Region of Russia
(Tsherepanov,1982).
#317
Ph.(Opsilia) tienschanica was described after two specimens: holotype
(male) from "Sussamyrgebirge, Ketmen Tjube" (Ketmen-Tiube on the south
bank of Toktogul water reserve, Kirizia) and a female from Narynkol. I saw
in Vienna both specimens from Fuchs private collection. Both specimens are
rather dark, but not black with distinct blue pubescence. They are sure
conspecific to numerous Ph. coerulescens collected by me in deifferent
parts of Central Asia (Alabel Pass - just near type locality, Karatau,
Chimgan, Kuramin Ridge, Zaamin Ridge, Nuratau, Samarkand, Piandzh, Marka-
Kol, Zyrianovsk). I am not sure if this form is conspecific to European
and Caucasian Ph.coerulescens.
#318
Ph. bucharica was described from "OST BUCHARA, Tschitschantan,
Nufswald, F.Hauser 1898" (two syntypes in collection of C.Holzschuh). The
locality is situated in Tadzhik area (Vorukh) southwards Isfara
(39°51'N, 70°35'E).
Ph. breuningi G. Dahlgren, 1988 was described after one female from
same series (Ost Buchara, Nusswald,Tschitschantan, F. Hauser, 1898), which
is preserved in Ebersvalde and was studied by me. So, Ph. bucharica = Ph.
breuningi.
Two such males from Tadzhikistan are preserved in collection of
C.Holzschuh (Gandzhino, Kizil-Kala, 1200m, 12-13.4.1978, V.Dolin leg.).
I've compared a big series of Opsilia (22 males and 14 females from
Afghanistan (Nurestan, N Waigal riv., 2000-3000m, IV-VII, 1971-73,
O.Kabakov leg.) with 4 Opsilia bucharica of C.Holzschuh. variability range
of Afghan series includes all known to me specimens of Ph. bucharica and I
do not see aven subspecific differences.
#319
Ph. prasina (described from Luristan) was recorded for Talysh
(Danilevsky, Kadlec, 1990). The record (Breuning, 1951) for "Buchara"
(Tadzhikistan?) is very doubtful.
One specially coloured female was collected by Miroshnikov in Armenia
(Gehard).
#320
After study of big series of Balcan Ph. vittipennis and Armenien Ph.
pravei I see the distinct constant differences, so I cancel the synonymy
published by Lobanov et al. (1981) and prefer now to return to
Plavilstshikov's position on two different species. Breuning (1951)
regarded both as subspecies.
I collected Ph. prawei in Turkmenia (8ex.: Kopet-Dag, Dushak
Mt.,1800m, 23.6.1992).
#321
The tribe Hippopsini was included in Agapanthiini by Breuning (1962,
1966). The genera Calamobius and Theophilea were regarded in Agapanthiini
(Breuning, 1966). This natural position was accepted by (Ñhemsak et al.,
1982).
#322
The typical A. violacea and A.intermedia from C. Europe (France and
Czechia) are really rather different (A. violacea without dense white
pubescence on metepisternum, long erect elytral setae are gradually
shortened backwards reaching apices; while in A. internedia long setae are
only near shoulders.
According to my materials from Moscow to Saratov only typical
A.intermedia are distributed.
In steppe area a variable taxon of transitional characters is very
numerous (species?). In my materials: from Kherson through Volgograd to
Ural valley.
In North Caucasus (Krasnodar and Stavropol regions) both forms
(violacea and intermedia are occue sympatrically.
In Crimea only A. violacea is distributed.
In Transcaucasie local forms similar to A. violacea are very common
as well as A. persicola (Talysh, Nakhichevan, Megri, Kafan, Agveran; a
series from Kopet-Dag collected from Runex), differing dense white
pubescence of metepisternum (in A. intermedia the episternal pubescence is
concentrared in line) and very dense erect elytral pubescence reaching
apices. All big Agapanthia from Transcaucasia belong to A. chalybaea, also
distributed in East and Central Anatolia (A. osmanlis, described from
Stambul env., absent in Transcaucasia - I've got it from Bulgaria and
Hungary). A. chalybaea can be green, blue and metallic-gray. Besides a
small bright-green Agapanthia is very numerous in Khosrov, with very rough
pronotal punctation, episternum pubescence like in A.intermedia, but with
numerous erect elytral setae (new species?).
The easten most locality of A. intermedia in my materials is in
Karaganda environs.
Rather typical A. violacea is in my materials from Zailiisky Alatau
(Talgar), Dzhungarsky Alatau, Tarbagatai.
In South Kazakhstan and Kirgizia (Chimkent, Karatau, Talassky Alatau,
Chu-Ili Mts., Ily River Valley, Bishkek env.) A. talassica (described as
A. violacea talassica). Series of syntypes is preserved in my collection
(2 males and 2 females, S. Kazakhstan, Talassky Alatau, Daubaba, 15.4.62,
22.4.62, 7.5.1962, A. Badenko leg.). The species is close to A. persicola,
but erect elytral setae are rather long au to elytral apices.
A. incerta described from Tadhikistan is close to A. talassica, but
well differs by very big eyes; no other blue Agapanthia in Tadzhikistan.
It is also known from near Samarkand.
#323
A. muellneri and A. soror were recorded for Kazakhstan (Zailiisky
Alatau) by Kadyrbekov and Tleppaeva (1997); both species were mentioned by
Kostin (1973,1978), but without exact data. Rhagium inquisitor, Saperda
perforata, Xylotrechus rusticus were also recoded for Zailiisky Alatau.
A. soror, S. perforata, X. rusticus were recorded for North Tian-Shan
by Kadyrbekov (1999).
#324
I've studied the the syntypes of Agapanthia bucharica in Paris. Both
small bright females are identical to A. detrita, so A. detrita = A.
bucharica. They are a little similar to A. kirbyi, which is absent in
Central Asia, and have no connection with A. hauseri. So position of
Breuning (1961), hausery = bucharica (accepted by Lobanov et al., 1981)
was wrong. The similarity to A.kirbyi, which was also stated in the
original description is connected with relatively uniform elytral
pubescense. The old name of type locality "Buchara" is most probably
connected with modern Tadzhikistan (see, for example, Semenov-Tian-
Shansky, 1935).
Plavilstshikov (1968) regarded the taxon as a species with special
record for Chardzhou (Turkmenia).
In my description of A. obydovi Danilevsky, 2000 I supposed the
occurense of A. detrita in Dzhungarsky Alatau based on Plavilstshikov's
(1968) record for Panfilov (Dzharkent). Now (2002) I can prove it for
Koksu River Valley (one female, 8.6.2001, O.Gorbunov leg.). I've also got
a pair of A. detrita from Ketmen Ridge (Podgornoe, 2.6.2001, O.Gorbunov
leg.). The species is also distributed along Zailiisky Alatau: a pair from
Syuktobe Mt. (18.5.2001, Danilevsky leg.), a male from Talgar (17.5.1967,
Falkovich leg., collection of ZIN).
#325
A. lateralis was recorded for USSR (Lobanov et al., 1982) on the base
of old doubtful data (Pic, 1910; Reitter,1898) and must be exluded from
the list of the region.
#326
According to Hayashi (1979) Leptura doii was described from "Etorofu,
S.Kurile Is." and is a synonym of L. aethiops. L. doii was recorded as a
species for Iturup Is. by Krivolutzkaia 1973 and then based on this record
for USSR by Lobanov et al. (1981). The taxon was restored by Kusama snd
Takakuwa (1984) with larger data on type locality: "Is. Etorofu, Kurile
Isls., Hokkaido". The restoration was not suppoted by Ohbayashi et al.
(1992).
#327
Eutetrapíà sedecimpunctata = Saperda motschulskyi (Tsherepanov,
1985).
#328
According to Danilevsly (1988c), Agapanthia auliensis Pic (described
from Aulie-Ata = Dzhambul = Taraz) is a valid name for the species wrongly
identified by Plavilstshikov (1968) and Kostin (1973) as A. angelicae. The
species absent in Turkmenia and Uzbekistan; it is distributed in
Kazakhstan from Muinkumy to Ily River Valley. I've got big series both
from near Taraz and from near Kapchagai and can not see any differences.
Becouse of this old mistake the species was described from Ily Valley
once more under the name A. amabilis Holz. I've seen the type series and
have specimens from Holzschuh's collection, so A. auliensis = A. amabilis.
Recently several localities of A. auliensis were published
(Kadyrbekov et al., 1998). Together with known localities (Taraz environs,
Muiunkumy Desert northwards Tatty and Kapchagai) two new were discovered.
First: NE Kyzylkumy, Karatau Mts westwards Syr-Darja near Bairkum
(10.5.1992). The locality is so far from the known area, that the species
identification needs to be checked. Second: Almaty region, 18km eastwards
Aksuek (24.4.95). I often observed here a lot of A. obydovi on Eremurus
sp., and the presence of another species on Eremurus seems to be very
doubtful.
#329
The date of A. altaica songarica was wrongly mentioned by Lobanov at
al.(1982) and by Tscherepanov (1984: 170 - as "songorica") as 1978. The
subspecies was described as A. dahli songarica Kostin, 1973 (a series of
syntypes from Chernaia Rechka near Lepsinsk in my collection) and in fact
is a local form of A. alternans, as well as A. altaica tarbagataica (a
series of syntypes from Aktugai in Tarbagatai in my collction). So, A.
aternans = A. d. songarica = A. a. tarbagataica.
According to my (23.6.2002) observations, A. dahli in North and East
Kazakhstan and in West Siberia (from Cheliabinsk and Kurgan to
Petropavlovsk, Ust-Kamenogorsk and Dzhungarsky Alatau is connected with
Malva; A. alternans is always monophagous on Prangos; while A. altaica is
connected with Pionaea (Plavilstshikov, 1968; Tsherepanov, 1984).
So A. altaica must be excluded from Kazakhstan fauna.
#330
A. villosoviridescens was wrongly recorded by Lobanov et al. (1982)
for Far East Russia and East Asia without any reasons. According to
Tsherepanov (1984), A.villosoviridescens = A. daurica.
#331
According to personal communication of Zahaikevitch (1982), he
identified Vadonia bisignata Brulle. from near Kishinev. According to
personal communication of J.Vorisek (1992), this statement is impossible,
because V.bisignata is known only from Peloponnessos and Thessalonike. It
could be V.moesiaca, known from Rumania.
#332
Rhopaloscelis caucasicus Danilevsky (nomen nudum), mentioned by
Lobanov et al. (1982), was marked out on the base of wrong identification
of Rh. schurmanni.
#333
According to personal communication of Zahaikevitch (1983), in
Cerambycinae several supertribes could be criated: Cerambycites,
Rosaliites, Callidiites, Clytites, Callichromites, Molorchites. The last
supertribed is the most specialized one.
#334
Dorcadion leopardinum was recorded for USSR by Lobanov et al. (1982)
without any reasons (Danilevsky, 1988d).
#335
The separation of Callidium aeneum in subgenus Callidostola was
accepted by Winkler (1929), Kusama and Takakuwa (1984) and others. For
Villiers (1978), Bily and Mehl (1989) it is a genus.
#336
The genus Trichoferus was sometimes regarded (Villiers, 1946) as a
subgenus of Hesperophanes.
#337
According to Rose (1983), Penichroa is in Hesperophanini.
#338
The type species of Olenecamptus, according to Lobanov et al. (1982)
is O. serratus Chevr., according to Gressitt (1951) is O. serratus Chevr.,
1835 = bilobus F., according to Plavilstshikov (1958), is Saperda bilobus
F., 1801.
#339
Oplosia suvorovi was regarded as a species by Tsherepanov (1984).
According to Tsherepanov (1984), it is distributed not only in Japan, SE
Siberia (Amur Region in my materials) and Far East of the continental
Russia, but also in Sakhalin Island, Korea and China (no references to any
publication or materials).
#340
Agapanthia lais Reiche 1858 was described from Balkan Peninsula ("du
Peloponese") and absent in Central Asia. It was recorded for Tadzhikistan
by Plavilstshikov (1968), Lobanov et al. (1982) because of wrong
identification of A. incerta.
#341
According to the study of the type series of Chlorophorus
motschulskyi chasanensis Tsherep.,1982 form Khasan Lake by A.Lobanov
(personal communication of 1987) it is a synonym of the nominative form.
#342
Special reference must be made in the case when the original
description was prepared by the author, who was not the author of the
publication.
#343
Due to unpredictable and unprecedented delay of the publication of my
aticle (Danilevsky, 1987) by "Revue d'Entomologie de l'URSS" more than for
3 years, all new names of this paper were published in the key by
Danilevsky and Miroshnikov (1985) without full description, photographs
and type materials. So, the type materials, published in 1987, were
represented by lectotypes and paralectotypes.
#344
According to Danilevsky (1999d), Exocentrus curtipennis Pic 1918
recorded for USSR by Plavilstshikov (1932), Lobanov et al. (1982), was
previously described as E.fasciolatus Bates, 1873 (Breuning, 1958) from
Japan and absent in Russia.
#345
According to Danilevsky (1988a), O. scutellaroides Br. = O. chinensis
Tsher.
A series of "Oberea chinensis" in Tsherapnov's collection consists of
two species: pale specimens are O. herzi, dark specimens are O. morio; but
no O. scutellaroides.
I've got a big series of O. scutellaroides from Russia (Ussuri-Land,
Barabash-Levada, 2-4.6.1989, S.Nikireev leg. and same locality, 24-
30.5.1989, D.Obydov leg.).
#346
Arhopaloscelis bifasciatus (as Rhopaloscelis) was recorded for
Sakhalin and Kunahir by Tsherepanov (1984).
#347
Euribatus gravidus was placed in USSR list by Lobanov et al. (1981)
on the base of Heyrovsky (1952) record: "Turcmenia, Kara-Kum Wuste", which
is unbelievable.
#348
E. chrysargirea was recorded by Krivolutzkaia (1973) for Kuriles on
own materials and then by Lobanov et al. (1982). It was evidently wrong
determination of E.chrysochloris (which was "absent" in Krivolutzkaia's
materials). She included in the area of her "chrysargirea" East Siberea,
so joined island species to continental E. metallescens. In fact E.
chrysochloris chrisargirea (described from Honshu) is a south Japan
subspecies (Kusama, Takakuwa, 1985) and absent on Kuriles, Hokkaido and
the continent.
#349
According to Villiers (1978), American genus Cyrtophorus absent in
Palaearctic Region. If it would be necessary to separate A.bicallosus and
A.gibbosus in Anaglyptus s.str., then other subgenus needs a new name.
#350
According to J.Vorisek (personal communication of 1992), he has
Dorcadion scabricolle and Dorcadion similar to D.argonauta from Kara-Kala,
D. holosericeum from Chuli. All specimens were "collected" by Potopolsky
(Ashkhabad) - the data are unbelievable.
#351
According to Lobanov et al. (1981), Xylotrechus rufilius = X. irinae,
that was accepted by Tsherepanov (1982).
X. magnicollis, described from West China (and known from Taiwan to
Burma and Assam), was recorded for Russia by Gressitt (1951) and Hayashi
(1992) on the base of synonymy: X. magnicollis = X. irinae. The species
identity of X. rufilius and X. magnicollis is rather possible (according
to my series from Taiwan).
#352
According to Miroshnikov (personal communication of 1993):
D. ciscaucasicum = D. mokrzeckii
Dorcadion "cinerarium" from Taman peninsula is D. panticapaeum. The
record was published by Kasatkin and Arzanov (1997).
#353
According to Miroshnikov (personal communication of 1993), old
materials collected by Vostrikov are often with strange (and wrong)
locality data:
D. elegans - Elisavetpol (= Kirovabad = Giandzha)
D. wagneri - Tersk. Region, Naurskaia
D. scabricolle - Grosnyi
#354
According to J.Vorisek (personal communication of 1992), A.
pavlovskii must be placed in subgenus Protapatophysis Sem. et Schegl.-Bar.
1935, but in fact it has no special characters: female coxae are widely
separated as in Apatophysis s.str., males and females without glabrous pad
line of all tarsi joints, 3d tarsi joints are with sharp lobes.
#355
According to E.Vives (2000) Penichroa fasciata (desribed as
Callidium fasciatum Stephens, 1931, not Herbst, 1784, not Billberg, 1817)
must be replaced with P. timida (Menetries, 1831). The necessaty of the
name change must be checked in agree with Article 23.9.1. of ICZN (1999).
#356
According to P. Svacha in Svacha, Danilevsky (1989: 19), Strangalia =
Strangalina.
#357
According to Tsherepanov (1987):
Stenocurus quercus was recorded for West Saian Mts. (so probably is
also
distributed in West Siberia?).
Anoplodera rufipes was recorded for West Saian Mts. (so probably is
also
distributed in West Siberia?).
Phymatodes testaceus was recorded for Altai (Maima River, 5km from
Kyzyl-Ozek)
#358
Several wrong records for Tadzhikistan were made by A.K.Kadyrov
(1989), sometimes with wrong references to Semenov-Tian-Shanskij (1935).
The following reported species absent in Tadzhikistan:
Pogonarthron tshitsherini (recorded as Prionus)
Polylobarthrom margelanicus (: as Prionus)
Dorcadion turkestanicum
Agapanthia violacea
Agapanthai lais
Under the names Oberea erythrocephala and O. ruficeps most probably
one species was recorded - O. ruficeps muchei. For both species Saccharum
officinarum was recorded as a food plant, while up to now they are known
only from Euphorbia.
#359
Volume 9th of Rev.Russe d'Entom. with Suvorov's descriptions of 1909
has on the title another date - 1910.
Volume 10-th of Rev.Russe d'Entom. with Suvorov's descriptions of
1910 has on the title another date - 1911.
Volume 11-th of Rev.Russe d'Entom. with description of Rosalia
coelesthis Sem. and Suvorov's descriptions of 1911 has on the title
another date - 1912.
#360
There is a male of Alosterna scapularis from Kopet-Dag in Zoological
Museum, St.-Petersburg (Nukhur, Transcaspian Reg., Archman env., Christof
leg.).
#361
Eodorcadion humerale (Gebler, 1823; Mem.Soc.Nat.Moscou), but not E.
humerale (Fischer-Waldheim, 1823; Mem.Soc.Nat.Moscou), as it was published
by Breuning (1961), though Fischer-Waldheim (1823) also published the
description of Dorcadion humerale, but in his "Entomographia Imperii
Rossici" and with reference to Gebler.
In Gebler's description the type locality was mentioned precisely ":
in pratis fabricae Petrovsk prope Werchnei-Udinsk."
The pictures to "Entomographia imperii Rossici" vol.2. 1923-24 by
Fischer-Waldheim were published before (1923). So the date of new names is
1923 if they are illustrated, if not - 1924.
#363
The date of Dorcadion glycyrrhizae (Pallas), published as Cerambyx in
"Reise durch verschiedene Provinzen des Russischen Reichs, T.2", is 1773,
as it was shown in the references to the article by Danilevsky (2001a),
but not 1771, as it was wrongly mentioned in the title of the article and
in its text (pp. 1-4). The mistake was left in the paper after first
version of my text based on Breuning (1961) data.
The original spelling "glicyrrhizae" restored by me
(Danilevsky,1999), must be forgotten according to the Article 33.2.3.1. of
the ICZN (1999). The general accepted spelling "glycyrrhizae" must be
used.
#364
It is not evident that Rhamnusium bicolor and Rh. gracilicorne are
different species. But if they are different (Villiers, 1978), then Rh.
bicolor is distributed only in West Europe.
#365
There are two similar Cortodera ruthena from near Aktiubinsk in
collection of P.V. Romantzov (St.-Petersburg) - yellow elytrae, black legs
and abdomen.
Male: Temir valley, Pokrovsky 22.5.2000 Romantzov leg.
Female: Karahobda River, Alpaisai 26.5.2000 Romantzov leg.
#366
A pair of Grammoptera gracilis were collected on Sakhalin by R.V.
Filimonov (Sakhalin, Susunai Ridge, 10km E Novoalexandrovsk, 29.06.91).
#367
Tetrops formosa was described from Issyk-Kul (Kirgizia). I've seen
(2002) several specimens of T.fomosa in Heyrovsky's collection (Prague)
with labels: "Kreise Karakol, Issyk-Kul, 2.6.31, V.Parfentiev" and "Issyk-
Kul, Terski-Tau, 6.1902, coll. Hauser".
Tetrops formosa bivittulata Jankowski, 1934, described from Zailiisky
Alatau (Alma-Ata) as a variation differs from the nominative subspecies by
dark general colour and specially by usual presence of elongated elytral
black spots. It was regarded as a subspecies distributed in Zailiisky
Alatau by Kostin (1973: 206) under the name "T. formosa bivittulata Plav."
Wrong attribution of the name to Plavilstshikov was repeated by Lobanov et
al. (1981: 790-791) in the wrong synonymization: "Tetrops formosa formosa
Baeckm., 1903 = T. formosa bivittulata Plav., 1954 (sensu Kostin, 1973)".
T.f.songarica (Dzhungarsky Alatau) has just same colour as T.f.
formosa. The differences between these two very distant subspecies are not
clear yet because of too small number of known specimens.
O. Mehl reared a series of Tetrops formosa ssp.n. from Malus twigs
collected (1991)near Arslan-Bob in Fergansky Ridge (Kirgizia). Specimens
are daker than T.f.formosa, but in general lighter than T.f. bivittulata,
though black elytral stripes are often present.
The statement of Kostin (1973), that in Ily valley two Tetrops
species: "T.plavilstshikovi" (=elaegni) and T. formosa songarica live
together is wrong. According to his materials in Zoological Museum (S.-
Petersburg), he identified less pubescent T.elaeagni from Ily valley as T.
formosa songarica. So T. f. songarica is distributed only in Dzhungarsky
Alatau and absent in Ily River valley.
T. elaeagni seems to be first recorded for Russia by Althoff,
Danilevsky (1997). I've put this record on the base of my two specimens
from Dzhanybek, which is situated exactly on Russia-Kazakhstan border. The
species is also known from Amu-Darja River Valley in Turkmenia (see
Kostin, 1973: 207).
#368
The iterpretation of two species of European Stenostola is different
in different publications. According to Bily and Mehl (1989), the species
with more developed metallic lustre and rough elytral punctationis is S.
ferrea ("Body black with slight metallic lustre. Elytra with coarse
punctuation." Villiers (1978)accepted same position: "Corp d'un noir
ardoise, a net reflet metallique." But for Bense (1995) S. ferrea: "Elytra
macroscopically without a blue metallic shine; :", and S. dubia: "Elytra
macroscopically with a distinct blue shine; :". This position was accepted
by Heyrovsky (1955), Plavistshikov (1965) and many other authors incuding
Danilevsky and Miroshnikov (1985 - so S. ferrea maculipennis Holz. belongs
to European species with less metallic lustre, finer punctuation and
denser pubescence). That is why all faunistical records of two species are
doubtful.
According to Plavilstshikov (1965) Stenostola in the European part of
the USSR was distributed southwards from the south of forest areas.
According to Bense (1995), Stenostola ferrea is distributed in Bultic
Republics; according to Alexandrovitch et al. (1996) Stenostola presents
in Belarus. I've got two males of S. dubia (sensu Bense) from Vladimir
Region (Kol'tchugino Distr., Zhuravlikha, on Salix caprea, 9.5.2001,
Svetlov leg.).
#369
One pair of Anaesthetis flavipilis (Barnaul env., Goretovskaia,
2.6.1901) is preserved now (2001) in Zoological Museum (St.-Petersburg).
According to the original description, two syntypes were collected in
Barnaul env. (10-13.6.1899 and 2.6.1901). The species is very similar to
A. confossicollis and differs only by yellow colour of pubescence. Both
Siberian species differs from A. testacea by big and scattered pronotal
punctuation.
Up to now A. flavipilis seems to be knowm only from type locality and
was never collected after original description.
The synonymisation of Breuning (1975): A. flavipilis = Mimosophronica
strandiella (which was described from Kuldzha) looks very doubtful.
All A. testacea from different parts of Caucasus (from Ciscaucasia to
Transcaucasia) differ from European specimens by longer pronotal
pubescence and denser pronotal punctuation. So they represent a separate
subspecies, which can be named A. t. rufescens Beckmann, 1903. The taxon
was described as A. t. var. rufescens from Beshtau Mt. (Stavropol Reg. of
Russia near Piatigorsk) after specimens with reddish head, antennae and
legs. Such coloured specimens are not rare in A.t.rufescens, but normally
colored beetles with black head, legs and antennae are more numerous.
Specimens from certain populations in Transcaucasia (Megri environs in
Armenia) have so long pronotal pubescence that are close to A. lanuginosa.
Similar specimens must be distributed in the south part of A. testaceus
Asian area.
#370
In Cenral Asian Republics Pilemia hirsutula seems to be represented
only in Turkmenia (as P.h.homoiesthes). In Kazakhstan it was recorded by
Kostin (1973) for west, center and south. I do not know the species from
South Kazakhstan, but if it is really distributed here, its subspecies
attribution is uncertain.
According to personal communication (2001) of R.V. Filimonov, he
collected P.h.hirsutula in Aktiubinsk Region of Kazakhstan (7ex., Temir
River Valley near Pokrovskaia, 5.1999 on Phlomis tuberosa), as well as in
Kurgan Reion of Russia (2ex., Ust-Uiskoe, 6.2000).
#371
The genus Turanium was revised by Danilevsky (2001e).
#372
The attribution of the name Stenocorus tataricus (Gebler, 1841),
described as Toxotus, to the species from Kirgizia and Uzbekistan by
Plavilstshikov (1936) was wrong (it was accepted by him after Reitter,
1907). In fact Toxotus tataricus was described from: "deserto ad fl.
Ajagus" (east Kazakhstan). S. "tataricus" sensu Reitter (1907, 1913) and
Plavilstshikov (1936), totally absent in Kazakhstan, as it was already
mentioned by Kostin (1973). In fact under the names Toxotus tataricus and
T. minutus Gebler (1841: 375 - both descriptions in one page!) described
big and small specimens of one species. It is really distributed from
Aiaguz River Valley and Ust-Kamenogorsk to Tarbagatai Mountains, Zaisan
Lake Valley and Markakol Lake Valley (so very possible in neihbour China
regions and in Russian Altai). The type locality of T. minutus was not
mentioned by Gebler, but T. minutus also originated from east Kazakhstan,
as all Gebler's desriptions of that paper were based on Dr. Screnk's
expedition (1840) materials "von Semipalatinsk aus in die sudostliche
Kirgisensteppe den Fluss Ajagus hinab zum See Balchasch, von da in die
sudosrlich um diesen See gelegenen Steppen und zu den sie begranzenden
Gebirgen Alatau und Tarbagatai :". I prefer to leave for this species the
name Stenocorus minutus (Gebl.), which was used for it by several authors
(Plavilstshikov, 1936; Gressitt, 1951; Kostin, 1973; Lobanov et al.,
1981). So, S. minutus = S. tataricus. Big specimens of S. minutus really
have round elytral apices as it was mentioned by Gebler, while for small
specimens obliquely truncate apices are more usual. Males and females of
S. minutus can be totally black, or black with pale-brown elytra, or also
with brown abdomen. Legs and antennae from totally black to totally brown,
often antennae apically as well as femora and tibia are darkened.
Both Stenocorus taxa from Uzbekistan and Kirgizia are characterized
by special antennal structure with big and flattened joints. Sure this
character was not mentioned by Gebler for his T. tataricus and T. minutus.
Stenocorus "tataricus", sensu Plavilstshikov, is distributed in
Fergana Valley (Uzbekistan) and neihbour regions of Kirgizia: south slope
of Chatkal Ridge (Sary-Chelek, Sumsar) and SW slope of Fergana Ridge (Kara-
Alma). This taxon was described as Toxotus validicornis Pic. The name was
originally published without description (Pic, 1900), but with a short
geographical data: "? Turk." and was attributed by Pic to Kraatz. The
description of T. validicornis was published later (Pic, 1906), but
without locality. I have studied the holotype of T. validicornis in Paris
(2002). It is small male with totally brown elytrae, without geographical
label, but with the label indicated its origin from Kraatz collection.
Based on the morphology of the holotype I can suppose the type locality as
Fergana Valley with surrounding mountains. The holotype of T. validicornis
var. alaiensis Pic, 1906 (similar but bigger)described from Alai Mts is
also preserved in Pic's collection.
Another Central Asian Stenocorus was described as Stenochorus (sic!)
univittatus Reitter, 1913 from "Taschkent, Ala-Tau". The taxon is very
numerous on Chimgan Mt. (west part of Chatkal Ridge in Uzbekistan). Rather
special populations, which up to now are regarded as S. univittatus, are
known from Aksu-Dzhabagly Nat. Reserve (Kazakhstan) and Karatau Ridge
(Kazakhstan). I've got one specimen of S. univittatus from Kandara (Gissar
Ridge in Tadzhikistan).
The taxonomical status of S. validicornis and S. univittatus is not
evident. In general populations from near Fergana Valley are represented
by specimens with a little more dense elytral pubescence, and elytra are
always uniformly colored (black or brown). Specimens with longitudinal
yellow elytral stripes are not known from the area. From the other side
specimens from Chimgan Mt. are very often unicolored, and sometimes are
not distinguishable from specimens from Sary-Chelek. So, now I prefer to
regard both taxa as subspecies. The populations from Karatau Ridge and
from Aksu-Dzhabagly represent two another subspecies (not described yet).
The attribution of Gissar population needs new materials. I've also got
one totally black male with poorly pubescent elytra from the southmost
point of Fergana Ridge just from China border (Tar River), which
subspecies attribution is also not clear. Recently "Stenocorus univittaus"
(so, S. validicornis univittatus) was recorded for Zhetyzhel Mountains
(westernmost part of Zailiisky Alatau Ridge) from near Karakastek Village,
(10.6.1997, 1500m) after one female (Kadyrbekov et al., 1998). The species
attribution of this female rests unclear.
Toxotus tataricus Gebler, 1841 is the type species of Toxotochorus
Reitter, 1907 (monobasic), but in fact it was wrong determination of
Toxotus validicornis Pic, 1906: "Toxotus tataricus Gebl., den ich
wenigstens dafur halte, hat abweichend gebildete Fuhler; sie sind namlich
schon vom dritten Gliede an etwas abgeflacht und ihre au?eren Apicalwinkel
stumpfeckig vortretend. Ich errichte darauf die Sektion Toxotochorus nov."
So, according to the Article 70.3 of ICZN (1999) I regard T. validicornis
Pic, 1906 as the type species of Toxotochorus.
Toxotus turkestanicus Ganglbauer, 1889 described after 1 female: "aus
Turkestan" was regarded as a synonym of T. tataricus by Aurivillius (1912)
and Gressitt (1951), that was evidently wrong, because according to the
original description: "Flugeldecken :, auf Rucken mit 2 schwach erhabenen
Langslinien." I accepted here the synonymysation of Reitter (1913):
"Stenochorus" vittatus = S. turkestanicus.
#373
The name T. hauseri nigra Kostin, 1973 is homonyme (not Kraatz, 1859)
and must be changed.
#374
Tetrops rosarum was recorded for Mongolia by Tcherepanov (1985) and
Krivolutzkaia (in: Tsherepanov, 1996) without special comments. Most
probably the records were based on Tetrops mongolicus Murzin, 1977.
#375
I've got two males of Asias tuvensis from Mongolia: "North Mongolia,
Zuun-Erzu, 5.8.63", another locality is not readable (5.8.62).
#376
Cortodera holosericea was recorded for Rostov Region (Donleskhoz near
Shakhty-city, 13.6.96) and for Stavropol by D. Kasatkin (1998).
#377
Cortodera ruthena was recorded for two localities of Rostov Region by
D. Kasatkin (1998). He also mentioned it for Lugansk Region (first record
for Ukraine?), but without concrete data.
#378
Isotomus comptus was recorded for European Russia: Borisoglebsk near
Voronezh, 8.1984, A.Fomichev leg. (Arzanov et al., 1993; Kasatkin, 1998).
#379
Two interesting series of Dorcadion are preserved in the collection
S.Kadlec (Litvinov, Czechia):
1. Dorcadion g. glycyrrhizae, 2 males and a female: "Emba River
near Guriev, 6.1983, I.Kabak leg."
2. D. globithorax: "Kazakhstan, Shengeldy (eastwards Kapchagai),
10.V"
#380
According to the remark (2002) of S.Kadlec: if Plavilstshikov (1968)
was right, including A. subnigra Pic, 1890, described from "Georgie", in
A. subchalybaea Rtt., 1898, the name of the species must be A. subnigra.
#381
The name Rhabdoclytus for Clytus acutivittis Kr. was mentioned by
Plavilstshikov (1940: 493) with reference to Jakobson (1913, v.71, f.28).
According to personal communication by Kasatkin (2002), Rhabdoclytus
Ganglb. was mentioned by Pic(1900, Catalogue bibliographique et
sinonymique... p.64) with reference to "Cat. Mars: 479"
The name Rhabdoclytus is a senior synonym of Hayashiclytus and can be
valid.
#382
According to personal communication (2002) by D.Kasatkin, the record
of C. reitteri for Salsk by Plavilstshikov (1936) was connected with the
black female from "Salsk Distr., vill. Kichkin, 27 05 28" preserved in
Zoological Museum of Moscow Univ. (and unknown to me). Now it is Kichkino
of Zavetnoe Distr. in about 200 êì NE Salsk.
#383
Tetropium fuscum seems to be absent in the east of Asian continent,
but is known from Hokkaido. The remark by S.Bily and O. Mehl (1989: 91):
"from the Caucasus over Siberia to Japan" was not based on any data.
#384
According to many publications (Bily and Mehl, 1989; Burakovsky et
al., 1990 and others), the author of genus Prionus is O.F. Muller (1764).
#385
Pogonarthron = Pseudomonocladum according to Danilevsky (1999b).
I have identified one male of Pogonarthron minutum from
Tadzhikistan (Babatag Ridge, 15km SW Gissar, 600m, 9.6.2001,
A.Petrov leg., coll. of A. Petrov (Moscow University of Forestry).
#386
I have studied the holotype (male with the label: "Alexander
Gebirge") of Agapanthia alexandris in Museum National d'Histoire Naturelle
(Paris) in September, 2002. The taxon, described after 1 specimen from
"Asie Centrale: Monts Alexandre" (now Kirgizsky Ridge), was wrongly
regarded as a synonym A. muellneri (Plavilstshikov, 1968). The type
differs considerably from A. muellneri (described from near Tashkent; I've
see the type in Budapest; in my collection from Uzbekistan: Chimgan and
Aktash in Tashkent env., Kuramin Ridge and Kirgizia: Sary-Chelek, Naryn
Ridge) by very dense and bright yellow elytral pubescence with very
distinct grey humeral stripe. I have collected a big series of A.
alexandris in Kazakhstan near Rgaity (south part of Chu-Ily Mountains,
9.6.2002). Some of new specimens with poorly developed humeral stripe. The
records of A. muellneri for Zailiisky Alatau could be based on A.
alexandris.
#387
According to C.Holzschuh (1999: 11), Pseudalosterna elegantula
(mainland) and P. misella (Japan) are different species. No Pseudalosterna
are known to me from Sakhalin or Kuril Is.
#388
P.Svacha (personal communication, 2002) received from Japan the
larvae of Nupserha marginella from Cirsium
#389
As it was mentioned by me before (Danilevsky, 2001: 18b) the size of
Cortodera haemorhoidalis (= C. analis) mentioned by Pic as 13-14mm was too
big for C. analis. In September 2002 I have studied the unique female of
C. haemorhoidalis in Pic's collection (Paris). It is normal C. analis with
red antennae, legs and abdominal apex. The specimen with labels:
"HOLOTYPE", "Siberie", "ex coll. Gebler" is 11,5 mm long, so big, but not
unusual.
I've also studied the holotype of C. analis var. ruficornis described
from "Altai". The small black female with reddish anterior legs and
antennae has a label: "Telezk See, Altay, Gessner". Teletskoe Lake was not
mentioned before as a locality of C. analis and is situated far eastwards
from the reliably known localities.
#390
Semiangusta was restored as a separate genus by Sama and Rejzek
(2002)with the desination of Conizonia delagrangei Pic, 1891 as its type
species. Phytoecia pici and Ph erivanica were excluded from Semiangusta.
Now both could be placed to Ph. (s.str.), as it was done by Breunig
(1951). So, Semiangusta absent in the territory of USSR.
#391
Anoplophora glabripennis was recorded for Khabarovsk Region of Russia
by Lingafelter and Hoebeke (2002). The map of its area includes a dot
(with question mark) near north part of Bureinsky Ridge (without any
comments in the text). Several China localities of the species are
situated just on the border of Russia: at the lower part of Argun River
Valley (Chita Region) and in the middle part of Ussuri River (Primorsky
Region).
#392
Dinoptera minuta (described from Nerchinsk) seems to be absent in
Japan, where it is replaced by very close Dinoptera criocerina (Bates,
1873). D. minuta was recorded for Sakhalin by Plavilstshikov (1936) and
Tsherepanov (1979, 1996). Both species absent in Hokkaido and Sakhalin.
#393
The taxon was described as "Leptura (Pachytodes) erratica race
bottcheri" from "Altai" after one specimen with rather black elytra
(yellow colour is represented by small spots only), and was regarded as a
China subspecies of Anoplodera (Pachytodes) erratica by Gressitt (1951). I
do not know such specimens, but still Pachytodes erraticus from Altai (Ust-
Kamenogorsk environs) differs from European and Caucasus populations
considerably: abdomen and elytral apex never reddish, yellow elytral
colour much paler. So, easten populations (eastwards Urals?) represent a
subspecies named preliminary as P.e. bottcheri.
#394
A. altajensis ussuricus was described from near Ussuriisk (South of
Primorsky Region). In the original description the taxon was compared with
the specimens of Amarysius from West Siberia collected from Spiraea and
wrongly regarded by the author as A.a.altajensis. Later Tsherepanov (1980)
explained his mistake and described the taxon from Spiraea as A.
duplicatus distributed in Salair Ridge and Tuva. On the base of this
situation A.a.ussuricus was cancelled by Lobanov et al. (1981: 789), and
Tsherepanov (1982) accepted the synonymy: A. altajensis = A. ussuricus.
In 2002 I've collected a lot of A. altajensis in about its type
locality near Ust-Kamenogorsk. The specimens of the nominative population
differ from the easten specimens (in my materials from Buriatiya and Chita
Region to Primorie Region) by different pronotal sculpture and different
shape of black elytral field, which often reachs scutellum and usually
notched posteriorly. So the easten subspecies A. a. ussuricus must be
restored.
A. duplicatus, described from Salair Mts. (near Novosibirsk) and
Tuva, was recorded for Far East Russia (Amur Region and Primorsky Region)
by Danilevsky (1998a) and so must be distributed in East Siberia, North
China and probably in Mongolia. Three males from Kazakhstan (Ust-
Kamenogorsk env.) are represented in my collection. Here both Amarysius
species occur sympatrically.
#395
Breuning (1975: 25; 1963: 518, in Breuning, 1958-1969) used wrong
spelling "P. siewersi" of Pogonocherus sieversi Gangl., 1886: 139. The
species was described from Manglisi southwards Tbilisi.
The species was recorded for Crimea by Zahaikevitch (1991: 153).
#396
Pachytodes longipes was recorded for Altai by Plavilstshikov (1936)
and for Altai and Tuva by Tsherepanov (1979). In my materials the most
western locality is in Buriatia (Transbaicalia).
Pachytodes orthotrichus is definitely known from Tuva and Khakassia
to Irkutsk Region (Sarma River in my collection). The species must occur
in Mongolia, though up to now (2002) no exact records were published. It
was recorded for Mongolia and for West Siberia by Lobanov et al. (1981),
but without any comments.
The main distinguishing character of two species mentioned by many
authors is pronotal pubescence. Pronotum of P. longipes is always without
erect setae. But only males of P. orthotrichus have pronotum with erect
setae, in females erect setae absent. This fact can lead to wrong
identification of corresponding females. In reality females of both
species can be very similar, but in P. longipes antennae are usually
distinctly longer.
#397
The records of Chlorophorus sartor for West and East Siberia
(Plavilstshikov, 1940) seems to be rather doubtful and were not confirmed
by new materials. It was not collected in Siberia by Tsherepanov (1982).
#398
Tetropini were separated by Planet (1924) and supported by
Namkhaidorzh (1976) and Danilevsky, Miroshnikov (1985).
#399
Nivellia sanguinosa and Anastrangalia sequensi were regarded as
possible for East Kazakhstan (Kostin, 1973).
#400
Menesia albifrons was recorded for Altai by Tsherepanov (1985); M.
bipunctata was recorded for Mongolia by Namhaidorzh (1979); Menesia
flavotecta and Ropaloscelis unifasciatus were recorded for Mongolia by
Lobanov et al. (1982) most probably on the base of specimens which are now
not in my disposal.
#401
The record of Pidonia puziloi for Mongolia (Lobanov et al., 1981) is
rather doubtful.
The reasons for supposition of Dokhtouroffia nebulosa for Mongolia
(Lobanov et al., 1981) are not clear.
#402
The area of Amarysius sanguinipennis was enlarged eastwards by
Tsherepanov (1982) to Altai and Tomsk.
#403
According to Namhaidorzh (1972), all records of Eodorcadion brandti
for Mongolia are doubtful.
#404
Due to the courtesy of Dr. M. Hasegawa I've got the possibility to
study the article by S.Matsumura (1911) with many new descriptions from
Sakhalin Is. Many new names introduced in this paper were synonyms.
Stenocorus amurensis = Toxotus sachalinensis Matsumura, 1911
Acmaeops angusticollis = Acmaeops viridula Matsumura, 1911
Oedecnema gebleri = Leptura decemmaculata Matsumura, 1911
Nivelia sanguinosa = Leptura rubripennis Matsumura, 1911
Rhaphuma gracilipes = Clytanthus sachalinensis Matsumura, 1911
The name "Acanthocinus oppositus Chevr., 1879" (nomen nudum?) was
most probably connected with the species reported later as "A.
carinulatus" from Sakhalin, as the name "Acanthocinus oppositus,
Matsumura, 1931" was placed by Gressitt (1951) among the synonyms of his
"A. carinulatus".
The name "Leptura fulva" was most probably used for corresponding
forms of Anastrangalia sequensi.
At least two pairs of names used in this paper as names of 4
different species are now regarded as pairs of synonyms:
Asemum striatum = Asemum amurense
Leptura aethiops = Leptura aterrima
The name Leptura (Pidonia) shirarakensis Matsumura, 1911 was most
probably connected with Oedecnema gebleri, because of some characters
mentioned in the original description:
"Antennen schwarz, vom 6ten an bis 10ten Glieder an der Basis
rotlichbraun. : Elytren schmutziggelb, je mit 4 schwarzen Flecken, von
denen 2 nahe der Basis, ein anderer fast in der Mitte und ubrige an der
Spitze occupirend. : Lange 12mm. : Der Form nach Pachyta cerambyciformis
Schrank. etwas anliche."
Another Sakhalin species with elytral pattern, which can be similarly
described, is Judolia sexmaculata, but in J. sexmaculata antennal joints
can never be with yellow bases.
Kanoa granulata was recorded for Sakhalin (as Leptura granulata). The
species (widely distributed in Hokkaido) seems to be never recorded from
Sakhalin afterwards.
#405
Agapanthia alternans was wrongly regarded as a synonym of A. dahli by
Lobanov et al. (1981) following Kostin (1978). In fact it is not close to
A. dahli and can not be regarded as its subspecies (Kostin, 1973), as both
often inhabit one locality in East Kazakhstan (Ust-Kamenogorsk env.,
Samarka env.).
A. dahli was recorded for Mongolia by Lobanov et al. (1982). The
occurrence of the species in Mongolia does not look impossible as I have a
typical A.dahli from Khakassia (Maina southwards Abakan).
Several more interesting localities of A. dahli represented in my
collection: Russia: Novosibirsk, Altai (Chemal, Gorno-Altaisk), Kurgan,
Cheliabinsk; Kazakhstan: Petropavlovsk, Aktiubinsk, Astana, Arkalyk,
Chimkent, Chulakkurgan, Lepsinsk, Ust-Kamenogorsk, Zyrianovsk, Samarka,
Marka-Kol Lake, Ily Valley; Tadzhikistan: Revad in Zeravshan valley.
#406
Recently (2002) D.Kasatkin (personal communication) discovered
considerable differences between Agapanthia detrita and A. obydovi in the
structure on the internal sac of aedeagus.
#407
Enoploderes sanguineum was recorded for Rostov Region of
Russia by A.Miroshnikov (2000). Pyrenoploderes Hayashi, 1960 was
regarded as a subgenus of Enoploderes.
#408
Monochamus urussovi was recorded for North Caucasus by Kasatkin and
Arzanov (1997): "Piatigorsk, 11.6.1954".
#409
Due to the curtsy of D. Kasatkin, I received the manuscript of the
publication by Runich et al. (2000). The publication itself is still
inaccessible for us both. It conteins several important positions:
1. P. livida caucasica Dan. was recorded for Mashuk and Zheleznovodsk. The
taxon was never described, so P.l.caucasica Runich, Kasatkin, Lantzov,
2000 must be regarded as nomen nudum.
2. Dorcadion sareptanum and D.kubanicum (=D. sareptanum euxinum) were
recorded from same localities as sympatric (Kumgorsk, 19 IV 1950; Proval,
7 V 1949). The records were evidently based on red and black specimens
from one population. The border line between two subspecies of D.
sareptanum is not clear, but now I prefer to regard all D. sareptanum from
Caucasus as D. s. euxinum.
3. Agapanthia subhalibaea was recorded from Mashuk Mt.(7-
12.V.1947,18.V.1948,12.V.1949).
4. Phytoecia volgensis and Ph. tuerki were both recorded from Mashuk Mt.
Undoubtedly both records belong to one taxon represented by specimens with
red pronotum and black pronotum. According to my materials, in the region
from Dagestan to about Piatigorsk the specimens with pale-grey elytral
pubescence are dominated. So those populations can be regarded as Ph.
(Musaria) nigripes volgensis (described from near Volgograd.
#410
According to Kasatkin and Arzanov (1985), Aromia moschata ambrosiaca
is distributed in North Caucasus: Naur, Essentuki, Kislovodsk and
northwards to the lowest part of Kuma River Valley. The subspecies status
of those populations depends on the percentage of red thorax specimens.
All my specimens from Dagestan are with partly red thorax, but all
from Krasnodar Region are with green prothorax. According to A.Miroshnikov
(personal communication, 2002) specimens with partly red prothorax are
distributed in Krasnaia Poliana environs.
I've got a male of A. m. moschata from Turkmenia (Kopet-Dag). The
record of A. m. ambrosiaca for Central Asia by Plavilstshikov (1940) was
connected with A.m. cruenta.
A. m. cruenta was recorded (without any comments) for Kirgizia by
Ovtchinnikov (1996), but I am not ready to accept such data as reliable
(Danilevsky, 2000).
Very rare A. moschata specimens with red thorax and dark legs from
Fergana most probably represent a new subspecies.
#411
One male of Dorcadion beckeri from near Suchumi (4.4.1979, I.Sokolov
leg.) is preserved in my collection.
#412
Oberea euphorbiae was recorded for Transcaucasus by Heyrîvskó (1955),
for Caucasus by Tsherepanov (1985) and for North Caucasus by Kasatkin
(1999): male and female from Maikop (07.1954) preserved in Zoological
Institute (St.-Petersburg).
#413
Ph. varentzovi was recorded for Dagestan (Krainovka, 18.5.1963,
Vorobiov leg.) by Miroshnikov (1990a) - first record for Russia.
#414
Kasatkin (1998) recorded Ph. puncticollis for Dagestan (female from
Kurush, 5.4.1953) - first record for Russia.
Kasatkin (1999) recorded for Crimea: Dorcadion pedestre (Mt.
Chatyr-Dag) and Semanotus russicus (Ialta).
#415
Xestoleptura rufiventris was recorded for Far East Islands of Russia
by Lobvanov et al. (1981) without any comments (as Anoplodera). Now it
looks like a mistake.
#416
The synonymysation Leptepania = Molorchinus, as well as the
combination Leptepania okunevi was established by Namhaidorzh (1979).
Contemporary the species was recorded for Mongolia.
#417
The spelling Pseudallosterna (Plavilstshikov, 1936) was wrong.
Original spelling is Pseudalosterna Plavilstshikov, 1934.
#418
Only one species of Rhagium (Rh.i.inquisitor) was recorded for Crimea
(Bartenev, 1989). I regard three more species (Rh. bifasciatum, mordax and
sycophanta) as very possible for the region.
#419
Phytoecia stenostoloides, described from "Verkhneudinsk" (now Ulan-
Ude in Transbaikalia) and missed in Tsherepanov's (1985) monograph, was
recorded for far-east Primorie Region of Russia (Tsherepanov, 1996).
#420
Hybometopia was usually regarded in Saphanini (Aurivillius, 1912;
Plavilstshikov, 1940). The taxonomic affinities of Hybometopia out of
Sapahanini was shown by Mamaev and Danilevsky (1973).
Axinopalpis and Hybometopia were placed in Callidiopini by Lobanov et
al. (1981), but most probably wingless Hybometopia better must be
separated in a new tribe.
Penichroa was placed in Hesperophanini by Villiers (1978).
#421
Cerambyx hieroglyphicus Pallas, 1773 was described from "Siberia".
The taxon was accepted as easten subspecies by Breuning (1952: 177) and
Gressitt (1951: 554). It is characterized by constantly blue colour of
pale pubescence. It is agree with my specimens from Tuva and Russian
Primorie Region.
The subspecies was recorded for "Lappland" by Breuning (1952), so can
be distributed in North of the European part of Russia, as well as in
Norway, Sweden and Finland; for Sakhalin Is. by Matsushita et Tamanuki
(1935) - afer Gressitt (1951); and for Mongolia by Heyrovsky (1973b),as
well as for "Nordeuropa".
#422
According to A.Miroshnikov (personal communication of 2003), Brulle
(1832: 258) introduced: "Lamia (Morinus Serv. ined.) lugubris Fabr." and
"Lamia (Morinus Serv. ined.) funesta Fabr.", but in same publication in
"Errata": "Morinus, lisez Morimus". So the name Morimus Brulle, 1832 must
be used and proposal of G.Sama (1991: 126): "Morinus Brulle, 1832 =
Morimus Serville, 1835" can not be accepterd.
#423
According to A.Miroshnikov (personal communication of 2003), the
original spelling is Plagionotus bartholomei and Phytoecia bithynensis.
Both can not be accepted, as "bartholomaei" and "bithyniensis" are "in
prevailing usage" according to the Article 33.3.1 of ICZN.
#424
A.Miroshnikov (1998: 392), affirmed, that E. Reitter's "Fauna
Germanica. Die Kafer des Deutschen Reiches. 64. Familie: Cerambycidae" was
published in 1913 (and not in 1912 as it is generally accepted). So,
according to his personal communication (2003), several names must be
dated 1913:
Xylosteina [Xylosteini] Reitter, 1913: 5.
Megarhagium Reitter, 1913: 6 [Rhagium subgen.].
Lepturobosca Reitter, 1913: 17.
Lepturalia Reitter, 1913: 20.
Callidostola Reitter, 1913: 37 [Callidium subgen.].
Melasmetus Reitter, 1913: 39 [Phymatodes subgen.].
Phymatoderus Reitter, 1913: 39 [Phymatodes subgen.
Phymatodes (Poecilium) alnoides Reitter, 1913: 40 [Ph.(P.) alni ssp.].
Phymatodellus Reitter, 1913: 40 [Phymatodes subgen.].
Megasemum sharpi Reitter, 1913: 43 (syn. pro Megasemum quadricostulatum
Kraatz, 1879).
Hesperandrius Reitter, 1913: 44-45 (syn. pro Trichoferus Wollaston, 1854).
Xyloclytus Reitter, 1913: 46 [Xylotrechus subgen.].
Pseudosphegesthes Reitter, 1912: 50.
#425
According to A.Miroshnikov (personal communication, 2003),
Ganglbauer's "Bestimmungs-Tabellen der europäischen Coleopteren. VII.
Cerambycidae" and "Bestimmungs-Tabellen der europäischen Coleopteren.
VIII. Cerambycidae" were first published in "Verhandlungen der k. k.
zoologisch-botanischen Gesellschaft in Wien", 1881 (Bd. XXXI, S. 681-757,
Taf. XXII) and 1883 (Bd. XXXIII, S. 437-586).
Then same works were published as separata in 1882 [S. 3(681)-
79(757), Taf. XXII] and 1884 [S. 3(437)-152(586)] that caused a big
confusion in subsequent citations.
Here are several important names from original publications by
Ganglbauer (1881, 1883):
Ganglbauer, 1881:
Cyrtoclytus: 688, 736.
Parmenopsis: 693.
Cortodera pumila: 710.
Rhagium pygmaeum: 718.
Clytus arietis lederi: 730.
Paraclytus reitteri: 737. P. raddei: 737.
Icosium tomentosum atticum: 743.
Ropalopus lederi: 747.
Ganglbauer, 1883:
Neodorcadion: 437, 508.
Compsodorcadion: 437.
Dorcadion litigiosum: 454. D. transsilvanicum: 462. D. songaricum: 477. D.
semenovi: 479. D. tuerki: 486. D. plasoni (syn pro D. laeve Faldermann):
481. D. talyschense: 491. D. reitteri: 492.
Eodorcadion carinatum blessigi: 512.
Exocentrus stierlini: 530.
Leiopus pachymerus (syn pro L. femoratus Fairmaire): 532.
Acanthocinus elegans: 534.
Agapanthia lateralis: 541. A. lederi: 542. A. intermedia: 543. A. daurica:
544.
Phytoecia affinis boeberi: 559. Ph. affinis tuerki: 575. Ph. fatima: 570.
Ph. plasoni: 571. Ph. puncticollis stygia: 572. Ph. kurdistana: 572. Ph.
bithynensis: 573.
#426
According to Miroshnikov (personal communication, 2003) the original
spellings are - Dorcadion talyschense and Purpuricenus talyschensis.
The original spelling: "Dorcadion talyschensis" was used by Breuning
(1962) - so must be accepted, but the necessity to return to original
spelling of Purpuricenus talyshensis is not evident because of the Article
33.3.1 (ICZN).
#427
According to Miroshnikov (personal communication, 2003) the original
description of Exocentrus stierlini was published two times in 1883:
"Verhandlungen der k. k. zoologisch-botanischen Gesellschaft in Wien",Bd.
XXXIII: 530 and in "Wiener Entomologische Zeitung", II. Helf. 12. S. 298-
299. Taf. IV, Fig. 3. According to "Verh. zool.-bot. Ges. Wien" the type
locality is "Deutschland, Oesterreich", according to "Wien. Entom. Ztg."
-the type locality is "Europa media".
#428
According to A.Miroshnikov (personal communication of 2003), the
separata of Jakowleff's article "Nouvelles especes du genre Dorcadion
Dalm." from "Horae Soc. Ent. Ross."(t. XXXIV, p. 59-70) were distributed
in May 1899. So, Jakowleff (1899) is the author of:
Dorcadion ciscaucasicum: 1(59).
D. apicipenne 3(61). (so the name can be older than D. jacobsoni
Jakowleff, 1899).
D. bisignatum: 8(66).
D. phenax: 10(68).
#459
D. glaucum was described from "Persien" and was recorded for Talysh
Mts. (Breuning, 1962). It was recorded for Soviet Armenia and Soviet
Azerbaidzhan by Plavilstshikov (1958). But before Plavilstshikov (1948)
was not sure, that the species occurs in Soviet Armenia. In fact no
specimens exist from the territory of the former USSR with good collecting
data. Most probably D. glaucum was never collected here. It is rather
common in North Iran very close to Armenien border. In my collection it is
represented by two series:
IR (Azerbaidzhan), Pass 1900m, ca. 10km n Kaleybar, 30.5.1998, W.Heinz
leg.
NE Azerbaidzhan, Kaleybar, 2100m, 25.6.02, Th.Deuve leg.
#460
Ch. motschulskyi was recorded for Mongolia by Namkhaidorzh (1976:
208). One male with a label: "Verkhneudinsk [now Ulan-Ude] env, Berezovka,
21.6.1920" is preserved in my collection.
#461
In 2002 looking throug Heyrovsky's collection in Prague I've found
two syntypes of Dorcadion songaricum m. scopini described from Ketmen Mts
in Kazakhstan. In reality it is D. arietinum, described by me as D. a.
ketmeniense, so D.a. scopini Heyrovsky, 1966 = D.a. ketmeniensis
Danilevsky, 1996.
#462
As it was written to me by G.Sama (personal communication, 2003):
"Semenov (1914) introduced Asias a new name replacing Anoplistes Serville,
1833 not Westwood, 1831 (Diptera). I was able to consult Neave
(Nomenclator Zoologicus, 1939, 1: 216); according to it, Anoplistes was
described by Westwood only in 1835 (Anoplistes Westwood, 1835, London &
Edinb., Phil. Mag., 3(6) (34): 280). This is confirmed by Horn &
Schenkling, 1929 (Index Litteraturae Entomologicae, series 1, band 4:
1312) where any Westwood's paper dealing with Diptera is listed in 1831,
while is confirmed for 1835 the description of "Insectorum novorum
exoticorum". Phillos. Mag. (3), 6: 280-281"
So, the name Anoplistes Serville, 1833 is valid.
#463
Polylobarthron margelanicus is widely distributed in South Kazakhstan
(not mentioned by Kostin, 1973). It was collected in Karzhantau by
V.Lukhtanov (22-23.6.2000 - one male in my collection), in Keles River
Valley by me (21.5.2000 - one male), besides I've got a male with the
label: "Ala-tau, Kurdai, 26.11[?].1926".
#464
Pogonocherus species, which looks close to P. stierlini, from Far
East Russia differs considerably from European populations. It was
preliminary identified as P. dalbergianus (see Danilevsky, Miroshnikov,
1985: 353).
#465
Asaperda stenostola was recorded for Kazakstan by Lobanov et al.
(1982) most probably on the base of specimens from East Kazakhstan, which
now are not in my disposal. I've got a female from Altai Mts. (Chemal,
6.1988, E.Matveev leg.)
#466
Brachyta interrogationis was recorded for Georgia by Miroshnikov
(1990).
#467
Molorchus umbellatarum was recorded for Central Asia by Lobanov et
al. (1982) on the base of publication by Mamaev and Danilevsky (1975:
187). Later those materials were identified as M. semenovi (Svacha,
Danilevsky, 1988: 207)
The species was also recorded for South Urals by Tsherepanov (1981).
#468
Molorchus tianshanicus was recorded for Kazakhstan by Lobanov et al.
(1982) without any comments.
#469
Callimus angulatus was recorded for Ukraine (Carpathians) by
Zahaikevitch (1991: 154).
#470
Callimoxys gracilis was recorded for Central Asia by Lobanov et al.
(1982) without any comments. I've got a male from Turkmenia (Kara-Kala).
#471
Deilus fugax was recorded for NW Kazakhstan (Embulatovka River) by
Tsherepanov (1981).
#472
Ropalopus femoratus was recorded for Central Russia by Althoff and
Danilevsky (1997) without any comments. The species was recorded for SW of
USSR by Plavilstshikov (1965) and was mentioned by Zahaikevitch (1991).
#473
Traditionally (at least before 1993) Ropalopus nadari was often mixed
with R. mali. All R. nadari known to me were collected in Tadzhikistan,
but species is sure distributed in similar landscapes in Uzbekistan and
possibly in Kirgizia. The record of Ropalopus nadari for Aksu-Dzhabagly in
South Kazakhstan (Kryzhanovsky, 1974) was evidently connected with R.
mali.
The record of R. nadari for East Siberia by Lobanov et al. (1982)
seems to be just a mistake.
#474
I have collected a lot of Turanium rauschorum (with larvae) on
Atraphaxis sp. in South Kazakhstan (8.5.1998) near Rgaity (Danilevsky,
2001).
#475
Semanotus semenovi was recorded for Kazakhstan part of Talas Ridge by
Kostin (1973).
#475
Xylotrechus rusticus was recorded for Stalinabad (Tadzhikistan) by
Plavilstshikov (1955: 525).
#476
Xylotrechus pantherinus was recorded for Central Asia by Lobanov et
al. (1982) most probably by mistake.
#477
Agapanthia nitidipennis was described after one male from near
Tbilisi (Dzvari, 22.5.1975). I saw the holotype and received one specimen
from Holzschuh's collection: Azerbajdzhan, Besh-Barma (Zarat), 13.6.1979.
In my own materials the species is represented by series from Georgia
(Tbilisi,Tzhneti,Dzagvi,Mleta), Azerbajdzhan (Altyagach) and from
Daghestan: Rutul env., 24.6.2001, M. Ismailova leg.
#478
The subspecies rank of Agapanthia cardui pannonica was
established by J.M. Gutowski (1992)
#488
Due to the courtesy of Dr. Michiaki Hasegawa I received three
specimens of
Pseudanaesthetis rufipennis (Matsushita, 1933) from Taiwan (originally
described as Eupogonius).
Without any doubt P.rufipennis and my Ussurella napolovi belong to
one genus (species are different). The type species of Pseudanaesthetis:
P. langana Pic, 1922 described from "Tonkin" is not known to me, but it
seems to be not close to P. rufipennis because of elongate cylindrical
prothorax ( a very small color photo was puiblished by Lizhong Hua et al.,
1993).
Several publications (Gressitt, 1951; Nakamura et al., 1992) supposed
Eupogonius rufipennis Matsushita, 1933 = Hirayamaia fuscorufa Matsushita,
1937 (also from Taiwan).
H. fuscorufa is a type species of genus Hirayamaia Matsushita, 1937, which
soon received a new name: Falsoterinae Matsushita, 1938. So, if the
synonymysation is right, then at least: Falsoterinae = Ussurella.
Before the final dicision of the problem I keep the name Ussurella as
valid and transfer P. rufipennis into Ussurella.
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Last updated: March 11, 2003