Poecilimon djakonovi Miram, 1938

Kaya, Sarp, Çiplak, Battal, Chobanov, Dragan & Heller, Klaus-Gerhard, 2012, Poecilimon bosphoricus group (Orthoptera, Phaneropterinae): iteration of morpho-taxonomy by song characteristics 3225, Zootaxa 3225 (1), pp. 1-71 : 22-25

publication ID

https://doi.org/ 10.11646/zootaxa.3225.1.1

persistent identifier

https://treatment.plazi.org/id/592C87F9-732E-2360-FDA9-19935DA4FB45

treatment provided by

Felipe

scientific name

Poecilimon djakonovi Miram, 1938
status

 

Poecilimon djakonovi Miram, 1938 View in CoL ( Fig. 186 View FIGURES 185–186 )

P. djakonovi Miram, 1938: 352 View in CoL . Zool. Zhurnal 17: 351 (Russian)/365.

P. djakonovi Miram, 1938:331 View in CoL ( Bei-Bienko 1954).

Type information: Holotype —male; Northwest Caucasus, Sofiya River (tributary of Bolshoi Zelenchuk) and foothills of Oshten Mt. ( Bei-Bienko 1954).

Bei-Bienko (1954) considers P. djakonovi most closely related to P. oligacanthus (herewith considered synonym of P. similis ) and P. similis . We support this opinion though further consideration about its taxonomic status requires studying its song.

Remark: In OSF (2011/03/29) together with photos of a paratype of P. djakonovi (NHM) some photos of a specimen identified by Demirsoy (ZMB) are presented. However, from the large spiracle and the relatively small tegmina with black markings it is evident that the latter is not a member of the P. bosphoricus group. This specimen may represent a taxon related to P. varicornis .

Description: See Bei-Bienko (1954).

Distribution ( Fig. 186 View FIGURES 185–186 ): NW Caucasus, Abkhazia and NE Turkey ( Bei-Bienko 1954; Demirsoy 1975).

Poecilimon bischoffi Ramme, 1933 ( Figs 18 View FIGURES 15–22 , 37, 48, 65, 77, 93, 104, 121, 135, 153, 170, 175–184, 186)

Poecilimon bischoffi Ramme, 1933: 572 View in CoL .

Eupoecilimon bischoffi (Ramme) ; Ramme, 1951: 417.

Poecilimon bischoffi (Ramme) View in CoL ; Bei-Bienko, 1954: 338.

Type information: Holotype —male; Turkey, Trabzon, Polathane ( ZMB) (Holotype (stridulatory file) and photos of type material presented in DORSA were examined).

Material examined: Holotype —male; TURKEY: Rize province— 4 males, İkizdere, Ovit Mt., (40 o 41’ N, 40 o 24’E), 1627 m, 29.7.2010 (leg. S. Kaya) (in alcohol in AUZM), 8 males, 7 females, (40 o 43’ N, 040 o 36’ E), 1009 m, 13.07.2011, (leg. B. Çıplak, S. Kaya, D. Chobanov, E. Mahir Korkmaz) (in alcohol in AUZM); UKRAINE: Crimea — 1 male, Central Crimean Mountains , Angarskiy Pereval Pass, (44 o 45’ N, 34 o 20’ E) 765 m, 25.7.2010 (leg. D. Chobanov) (in alcohol in CDC). GoogleMaps

Description: For morphology see Table 1, 2 and Figures 18 View FIGURES 15–22 , 37, 48, 65, 77, 93, 104, 121, 135, 153, 170; for song see Table 3 and Figures 175–184 View FIGURES 175–176 View FIGURES 177–184 , 186 View FIGURES 185–186 . Additional description can be found mainly in Ramme (1933, 1951) and Bei-Bienko (1954).

Distribution ( Fig. 186 View FIGURES 185–186 ): This species is known from its type locality Turkey, Trabzon ( Ramme 1933) and Rize (present paper). The specimen collected from Crimea, at the opposite of Anatolia Black Sea coast, was tentatively placed under this taxon and further molecular studies may add to its systematic position.

Remarks: So far this species was known only from the type material and it is identifiable from P. similis by the typical apex of male cerci. New specimens from Rize Province ( Turkey) were identified as P. bischoffi by the cercal apex with the inner row of denticles being longer than the outer one. Some specimens from other localities show intermediate features between P. similis and P. bischoffi . Thus, it is difficult to doubtlessly distinguish both species. On the other hand, although the syllable pattern is similar in both species they differ from each other in several song parameters ( Figs 169 View FIGURES 167–169 , 170 View FIGURES 170–172 , 175–184 View FIGURES 175–176 View FIGURES 177–184 ), thus P. bischoffi is retained as a distinct species. Furthermore, a specimen collected at the opposite side of the Black Sea (Crimea) is similar to P. bischoffi both in morphology (especially male cerci) and song (Table 3 and Figures 170 View FIGURES 170–172 ). Though there are some differences in the shape of pronotum and song (syllable duration—see Fig. 175 View FIGURES 175–176 ), it was considered under P. bischoffi until new data is gathered.

Poecilimon scythicus Stshelkanovtzev, 1911 ( Figs 19 View FIGURES 15–22 , 49 View FIGURES 48–51 , 78, 105, 136, 154, 171, 175–184, 186)

Poecilimon scythicus Stshelkanovtzev, 1911: 18 View in CoL .

Type information: Unknown number of syntypes —males, females; Ukraine, SE, Proval'skii stud farm, Donetk Hills ( ZIN St. Petersburg) (not examined) .

Material examined: UKRAINE: Lugansk District — 2 males, Umg. Lugansk, Lugansk Reserve , (47° 21’ N, 37° 03’ E) 12.6.1996 (leg. A. Benediktow) GoogleMaps ; Donetska Oblast District — 2 males, 7 females, Goreliy Forest , 26.6.2006 (leg.?) (in alcohol in CDC).

Description: For morphology see Table 1, 2 and Figures 19 View FIGURES 15–22 , 49 View FIGURES 48–51 , 78, 105, 136, 154; for song see Table 3 and Figures 171 View FIGURES 170–172 , 175–184 View FIGURES 175–176 View FIGURES 177–184 . Additional description can be found in Ramme (1933), Bei-Bienko (1954) and Harz (1969).

Distribution ( Fig. 186 View FIGURES 185–186 ): This is the most widespread species in the northern Basin of the Black Sea present in Ukraine, Central and Southeast European Russia to Volga River and Western and Central Caucasus ( Bei-Bienko 1954; Zhantiev & Korsunovskaya 2005).

Remarks: Bei-Bienko (1954) presented a comprehensive description and a detailed account about P. scythicus and mentioned that it is similar to P. tauricus . Both species share the presence of syllable Type-3, but well differ in temporal parameters, which confirm the species status of both taxa.

Poecilimon tauricus Retowski, 1888 ( Figs 20, 21 View FIGURES 15–22 , 50 View FIGURES 48–51 , 79, 80, 106, 107, 137, 138, 156, 172, 173, 175–184, 186)

Barbitistes sanguinolenta Fischer von Waldheim, 1846 . Syn. by Bei-Bienko (1954: (nomen nudum)

Poecilimon tauricus Retowski, 1888: 408 View in CoL .

Poecilimon bosphoricus Retowski, 1888 View in CoL : Jacobson & Bianchi 1905; Kirby, 1906: 379 (both partim).

Poecilimon kusnezovi Miram, 1929: 463 View in CoL , syn.n.

Poecilimon beybienkoi Tarbinsky, 1932: 184 View in CoL , syn.n.

Poecilimon scythicus Retowski, 1888 View in CoL ; Bei-Bienko. 1941: 147.

Poecilimon ajpetri Stshelkanovtzev, 1911 View in CoL . Syn. by Bei-Bienko (1954).

Type information: Unknown number of syntypes —males, females; Krym, [Crimea: S, Dvukhyakornyi (near Koktebel), Krasnokamenka (Kiziltash) north of Otuz, Novyi Svet (west of Sudak) and Okhontich'e (Buragan)] (Beibienko 1954).

Material examined: UKRAINE: Crimea —for P. tauricus — 11 males, 8 females, Crimea, Western Crimean Mountains, Aj-Petri Yayla , (44 o 28’ N, 34 o 02’ E), 1250 m, 30.7.2010; for P. kusnezovi / P. beybienkoi — 13 males, 6 females, Western Crimean Mountains , Babugan Yayla, (44 o 36’ / 44 o 37’ N, 34 o 14’ / 34 o 17’ E), 1440/ 1360 m, 27.7.2010 (leg. D. Chobanov) (in alcohol in CDC) GoogleMaps .

Synonymy and description: This taxon has been described under several names (see the synonymic list above), the recent ones used being P. tauricus , P. kusnezovi and P. beybienkoi . During an extensive field trip over the mountains of South Crimea held in July 2010 material matching all these forms has been collected. From earlier literature data (e.g. Bei-Bienko 1954; Harz 1969; Zhantiev & Korsunovskaya 2005) it is very difficult to outline the range of these taxa; they were reported from same localities even in one paper, e.g. the couples P. tauricuskusnezovi from Babugan Yayla and P. kusnezovi-beybienkoi from Yalta (see last citations). Considering their very similar morphology misidentification may frequently be involved in these records. Subsequently, we collected typical P. kusnezovi and P. beybienkoi , as well as intermediate forms at the same place and habitat (Babugan Yayla); Bei-Bienko (1954) also investigated and reported both P. kusnezovi and P. tauricus from this place. The latter author (l.c.) has possibly concerned this as a proof that these are good species. However, we think this is not the case. We observed smooth transition in the shape of the tenth tergum ranging from typical kusnezovi to typical beybienkoi (see Fig. 4 View FIGURES 2–4 ). Male cerci were also quite variable in all populations, ranging from typical for kusnezovi / beybienkoi (Fig. 80) or tauricus (Fig. 79) to intermediate (compare Figs 79 and 80). The songs though having some differences between animals from different populations are generally very similar and yet quite variable (also unpublished data from laboratory reared animals). Finally, new records on possible hybrids between “typical” tauricus and kusnezovi , as well as unpublished data on the molecular phylogeny of the Crimean taxa (Chobanov et al., data in preparation) support the synonymic state of P. tauricus , P. kusnezovi and P. beybienkoi .

For morphological data of the species see the above given references, Table 1, 2 and Figures 20, 21 View FIGURES 15–22 , 50 View FIGURES 48–51 , 79, 80, 106, 107, 137, 138, 156; for song see Table 3 and Figures 172 View FIGURES 170–172 , 173 View FIGURES 173–174 , 175–184 View FIGURES 175–176 View FIGURES 177–184 .

Diagnosis: The species is most similar to P. scythicus and P. pliginskii . From both it differs in the shape of male cerci (cf. Figs. 79, 80 for tauricus with 78 for scythicus and 81 for pliginskii ). From scythicus it further differs in the well-expressed medial constriction of male pronotum with strongly widened pro-and metazona (cf. Figs. 20, 21 View FIGURES 15–22 with 22). From pliginskii ts differs also in the longer subgenital plate, which however in some cases may be obscure together with the cercus shape due to their variability. Unpublished data (Chobanov et al., data in preparation) support the strong genetic similarity of P. tauricus and P. pliginskii . Females of the three mentioned taxa cannot be distinguished.

Distribution ( Fig. 186 View FIGURES 185–186 ): Endemic to the mountains and south coast of Western Crimea —from Alushta and Babugan Yayla westwards.

Poecilimon pliginskii Miram, 1929 ( Figs 22 View FIGURES 15–22 , 51 View FIGURES 48–51 , 81, 108, 139, 140, 157, 158, 174, 175–184, 186)

Poecilimon tauricus Miram, 1929: 452 View in CoL (partim) ( Ramme 1933; Bei-Bienko 1954; Eades et al. 2011).

Poecilimon pliginskii Miram, 1929 View in CoL : Bei-Bienko, 1954: 349.

Poecilimon boldyrevi Miram, 1938: 363 View in CoL , 366, syn.n.

Type information: Holotype —male; Krym, [Crimea: South, Taushan-Bazar ] ( ZIN St. Petersburg).

Material examined: UKRAINE: Crimea —for pliginskii , 4 males and 8 females, Eastern Crimean Mountains, Echki Dag Mountain , (44 o 54’ N, 35 o 07’ E), 600 m, 22.7.2010 (leg. D. Chobanov) (in alcohol in CDC) GoogleMaps ; 8 males and 10 females, Crimea, Central Crimean Mountains, Chetyr Dag Mountain , (44 o 44’ N, 34 o 19’ E), 1250 m, 25.7.2010 (leg. D. Chobanov) (in alcohol in CDC) GoogleMaps ; for boldyrevi , 4 males, 8 females, Crimea, Northern slope of the Crimean Mountains , Krasnolesje village S of Simgeropol, (44 o 46’ N, 34 o 11’ E), 700 m, 30.7.2010 (leg. D. Chobanov) (in alcohol in CDC) GoogleMaps .

Synonymy and description: Bei-Bienko (1954) considered P. pliginskii and P. boldyrevi distinct taxa regarding mostly the shape of male cerci. We found considerable variation of this character (see Fig. 81) even in one place. For example, typical “ boldyrevi - type ” of cerci (Fig. 81A—specimen from Krasnolesje, Central Crimea) is almost identical with a specimen of P. pliginskii from Echki-Dag (near Karadag, Eastern Crimea) (Fig. 81E). The songs of both taxa (compare Zhantiev & Korsunovskaya 2005: Figs 10–11 View FIGURES 7–14 with 18–20) have identical syllable structure; the different syllable grouping varies in all Crimean taxa (see Figs 174–184 View FIGURES 173–174 View FIGURES 175–176 View FIGURES 177–184 ; unpublished data). Additionally, unpublished data on genetic phylogeny (Chobanov et al., data in preparation) support the identity of both taxa. The great variation and genetic similarity ( Ramme 1933; own unpublished data) suggest close relationships also of P. tauricus and P. pliginskii and their possible infraspecific relationships but we remain this question open until new data are gathered.

For morphology see Table 1, 2 and Figures 22 View FIGURES 15–22 , 51 View FIGURES 48–51 , 81, 108, 139, 140, 157, 158; for song see Table 3 and Figures 174 View FIGURES 173–174 , 175–184 View FIGURES 175–176 View FIGURES 177–184 .

Diagnosis: P. pliginskii is most similar to P. tauricus ; for differences see the latter.

Distribution ( Fig. 186 View FIGURES 185–186 ): Endemic to the South Crimea, occurring along the South coast and the mountains mostly in the eastern part of the peninsula; further records are known westwards to Taushan-Bazar.

ZMB

Museum für Naturkunde Berlin (Zoological Collections)

CDC

Changdu Institute for Drug Control

ZIN

Russian Academy of Sciences, Zoological Institute, Zoological Museum

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Orthoptera

Family

Tettigoniidae

Genus

Poecilimon

Loc

Poecilimon djakonovi Miram, 1938

Kaya, Sarp, Çiplak, Battal, Chobanov, Dragan & Heller, Klaus-Gerhard 2012
2012
Loc

Poecilimon bischoffi (Ramme)

Bei-Bienko G. Ya. 1954: 338
1954
Loc

Poecilimon pliginskii

Bei-Bienko G. Ya. 1954: 349
1954
Loc

Eupoecilimon bischoffi (Ramme)

Ramme, W. 1951: 417
1951
Loc

P. djakonovi

Miram, E. F. 1938: 352
1938
Loc

P. djakonovi

Miram, E. F. 1938: 331
1938
Loc

Poecilimon boldyrevi

Miram, E. F. 1938: 363
1938
Loc

Poecilimon bischoffi

Ramme, W. 1933: 572
1933
Loc

Poecilimon beybienkoi

Tarbinsky, S. P. 1932: 184
1932
Loc

Poecilimon kusnezovi

Miram, E. 1929: 463
1929
Loc

Poecilimon tauricus

Miram, E. 1929: 452
1929
Loc

Poecilimon scythicus

Stshelkanovtzev, J. P. 1911: 18
1911
Loc

Poecilimon tauricus

Retowski, O. 1888: 408
1888
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