Figure 4 - uploaded by Asmus Schröter
Content may be subject to copyright.
Male of Calopteryx splendens tschaldirica . Kura river southwest Khashu - ri, Georgia (29-vi-2014; photograph by Stefan Kohl) 

Male of Calopteryx splendens tschaldirica . Kura river southwest Khashu - ri, Georgia (29-vi-2014; photograph by Stefan Kohl) 

Source publication
Article
Full-text available
A total of 63 odonate taxa were recorded in Georgia during nationwide surveys in June–July 2014, and June and July–August 2015, corresponding to at least 85 % of the country’s Odonata fauna. For the majority of species information from Georgia is provided in English language for the first time. Selysiothemis nigra is a new addition to the country’s...

Context in source publication

Context 1
... the middle and upper course of the Kura river and its tributaries within the region of Samtkhe-Javakheti and bordering areas to the Shida-Kartli re- gion, we encountered a distinctly small and dainty form of C. splendens with comparatively narrow wings. Males had broadly hyaline wing apices and small rather diffuse blue spots not reaching the wing hind margin ( Fig. 4). While the wing spots faded out distally, their proximate border was distinc- tively clear cut and straight. The matt blue wing spots strongly varied in size and markedness and several males appeared to have almost entirely hyaline wings with traces of a blue tinge only. The length of the male’s abdomen was roughly a centimetre shorter than in average males of ssp. intermedia from the adjacent capital area (31 mm; n = 8, vs 40 mm in ssp. intermedia , n = 11). These males perfectly matched both the description and the distribution of ssp. tschaldirica Bartenev, 1909, described from specimens collected in 1909 within the former Kars Oblast ( Карсская область ) of the Russian Empire, on today’s Turkish territory (Ardahan and Kars provinces) at the source of the Kura river around Tschildir lake (” Чилдыр ”; Turk. Çıldır Gölü) (Bar- tenev 1909). We therefore assign this form to ssp . tschaldirica , which is in perfect accordance with descriptions and illustrations given by Dumont et al. (1987), who revealed the true nature and status of this taxon that had been unclear for decades. This was probably due to individual unjustified changes of its taxonomical status by Bartenev himself, who in 1912 treated it as a ssp. of the Selysian taurica (Bartenev 1912: 80; cf. Selys 1853). As stated by Dumont et al. (1987), available data suggest that ssp. tschaldiri ca is an altitudinal form centred on the volcanic plateau of the Ar- menian highland from where it penetrates into the lower regions towards the East along the course of the Kura, being replaced by ssp . intermedia roughly west of Mzcheta. The western limit of its Georgian range remains rather unclear; however, ssp. tschaldirica obviously does not enter deeply into Adjaria and the Colchic lowland, where it is largely replaced by ssp. mingrelica. What regards alleged ssp. tschaldirica reported from northeast of Batumi by Bartenev (1930a), see Dumont et al. (1987). Calopteryx virgo has been first mentioned from today’s Georgian territory by Eichwald (1837) in a report on his expedition across the Colchic low- land. He described the species as being abundant at brooks in forests of Mingrelia (sub Agrion colchicum ). Only a short time later C. virgo was re- peatedly reported from Mingrelia by Selys (1868), who stated that it cor- responded to Brullé’s taxon festiva . According to our data, Georgian C. virgo indeed generally correspond to ssp. festiva in all characters described by Brullé (1832), with all blackish wings in males and conspicuously dark winged females (Bartenev 1912b). The species appeared to be scarce and localised in Georgia and to be strictly confined to the lowlands in smaller abundances only. In adjacent Azerbaijan it seems to be very rare (Skvort sov & Snegovaya 2014) and it has never been recorded in Armenia so far (Tailly et al. 2004; Ananian & Tailly 2013). At loc. 60 we discovered a small population of C. virgo festiva with con- spicuously different looking females, which had brightened, entirely trans- lucent fore wings and two third translucent hind wings with contrasting dark tips and white pseudopterostigmata (Fig. 5). In single females the con- trast of this colour pattern was even more pronounced than shown on the photo and the basal borders of the dark tips were sharper delimited. These females were comparatively large (up to 54 mm total length) and, they strik- ingly resembled females of C. haemorrhoidalis , a western Mediterranean endemic. However, we also observed single typical coloured females flying syntopically with this form at loc. 60. In his publication on dragonflies of the former Kuban oblast, Bartenev (1910: 35) introduced the name »var. ♀ feminalis nov.« based on females collected at Goryachy Klyuch ( Горячий Ключ ) on the nortwestern foot- hills of the Caucasus range, north of Sochi, Russia. We here give the original quotation of the Latin description: »alae anteriores pelucentes concolores, posteriores triente apicali fasciâ introrsum rectilineatim atque argute termi- natâ adumbratae« [forewings unicolour translucent, the outer third of the hind wings with a straight-lined and clearly confined tinted band]. Barte- nev’s description thus perfectly matched our haemorrhoidalis -like Georgian females. Moreover, in the introduction Bartenev decidedly stated the simi- larity of his newly described female colour form of C. virgo to C. haemor rhoidalis females. We are therefore sure that our females correspond to Bar- tenev’s feminalis type females he collected some 300 km north of our site, within the same climatic and natural unit along the humid subtropical east- ern shore of the Black Sea. The nomenclatural status of feminalis can be derived from the fact that Bartenev introduced the name in combination with the term »var. ♀ nov..«. He therefore clearly intended to denote a new, female-linked variety defined upon the female only. Such third variety name in binominal taxa should be regarded as subspecific if ...

Citations

... «not rare up to 1000 m» [Kalkman, 2015] (that could mean that it occurs also at higher levels but rarely). That Atlas did not communicate the upper limits for A. juncea The two papers on the Odonata fauna of the adjacent Georgia [Schröter et al., 2015;Seehausen et al., 2016] do not provide elevation limits explicitly but the detailed information on the localities studied allowed us to infer them. Let us do this for species for which the European information was absent or vague. ...
... S. fl aveolum (L.) and L. quadrimaculata L. in Georgia is 2115 m a.s.l. [Schröter et al., 2015;Seehausen et al., 2016]. This is 700 m below Lake Debrishara, where populations of the two former species were found, and 405 m below Lake Bezdonnoe where the population of the latter exists. ...
... 1450 m and L. depressa L. 2105 m a.s.l. [Schröter et al., 2015;Seehausen et al., 2016]; in the fi rst case this is above and in the second and third cases below our Dagestanean records. In the mountains of Central Asia S. pedemontanum (Müll.) ...
Article
Full-text available
Published data on Odonata of Dagestan in highland habitats, that is situated above the tree line, were confined to registration in 1924–1926 of Aeshna juncea (Linnaeus, 1758) at Kurush village (the southernmost settlement of Russia). During the focused studies on the dragonflies of Dagestan in 2021–2023, we accumulated data on those of seven highland habitats situated in six districts at elevations of 2000–2800 m a.s.l., five of which are lakes or lake groups. Thirteen species from five families were revealed, including Cordulia aenea (Linnaeus, 1758) recorded in Dagestan for the first time, its habitat at 2525 m a.s.l. at Lake Bezdonnoe appearing the most elevated of those known for this species in the world. Elevation limits of other dragonflies of Dagestan are discussed. The huge population of A. juncea crenatoides Bartenef, 1925 of Lake Debrishara (2816 m a.s.l.) is unique in many respects: (1) the emerged dragonflies commence a downward vertical migration to the valley situated ca 400 m below; (2) about one quarter of specimens have an unusual pattern of the synthorax sides, with the additional pale stripe merging with the fore main stripe (the same morph was revealed in all specimens in populations in Armenia and South-eastern Turkey); (3) females thrice exceed males in number. Possible causes of these peculiarities are discussed.
... At the same time, the specimen from Ordubad District of Azerbaijan (sequence 16160) has normal, not reduced antehumeral stripes. The reduced stripe was observed in the neighbouring Georgia [53], eastern parts of Turkey (unpublished), while in some populations of Dagestan (Russia) and SE Turkey, individuals with both stripe versions fly together (unpublished). Both our analyses, of ITS ( Figure 2) and COI (Figure 3), did not reveal any divergence of the Balakan specimen from those from elsewhere; its COI sequence is most close to the specimen from Montenegro. ...
Article
Full-text available
Aeshnidae Rambur, 1842 are impressive large insects distributed worldwide. Currently, over 500 species are recognized. Nevertheless, the phylogeny of this family is not completely understood. We applied molecular phylogenetic analysis using two popular phylogenetic markers, the mitochondrial COI gene fragment (barcoding sequence) and the nucleic ITS region, containing the ITS1, 5.8S rRNA, and ITS2 sequences. We used available and credible published sequences and 96 newly sequenced specimens. Our analysis involved all West Palaearctic species, all but one genera of the Holarctic Aeshnidae, and most genera worldwide, and is by far the largest molecular study of this family. The topology of all trees created with different algorithms and genes is in favour of the current taxonomic concept, with some remarkable outcomes. Aeshna Fabricius, 1775, was found to be diverged into several branches, especially with respect to the COI gene. Although it appeared not monophyletic in phylogenetic reconstructions based on the ITS region, the analysis of COI and joint analysis suggest its monophyly in the current taxonomical sense, with one notable exception. Aeshna isoceles (Müller, 1767) has fallen out of Aeshna in all analyses, so a new monophyletic genus, Isoaeschna gen. nov. is introduced for it. The genus Brachytron Evans, 1845 tightly clustered with Aeschnophlebia Selys, 1883, Epiaeschna Hagen in Selys, 1883, and Nasiaeschna Selys in Förster, 1900. Thus, we suggest subsuming these four genera under the priority name Brachytron. Tetracanthagyna Selys, 1883 clusters as expected with Brachytron in the ITS tree, but is an independent ancient clade of its own in all COI trees. The genus Polycanthagyna Fraser, 1933 syn. nov. is synonymised to Indaeschna Fraser, 1926. On the species level, we suggest that the American Aeshna septentrionalis Burmeister, 1839 be treated as a subspecies of A. caerulea (Ström, 1783), Aeshna caerulea septentrionalis. We synonymize Gynacantha hyalina Selys, 1882 with Gynacantha subinterrupta Rambur, 1842. Our analysis provides new insights on the tight relationships of the circumboreal species Aeshna juncea and A. subarctica and the intraspecies phylogeny of Aeshna juncea.
... The habitats seem roughly to be confined within the Armenian Highlands and the eastern Taurus, east of the Anatolian Diagonal and west of the Lesser Caucasus (Fig. 6). Cordulegaster picta occurs west, north, and north-east of the Anatolian Diagonal in Georgia and Azerbaijan (Schröter et al. 2015;Schneider et al. 2021;Boudot et al. 2021). Available literature includes a record of C. picta in north-western Iran (Rastegar et al. 2013). ...
... 33b). Such 'intermediate' males were recently reported from Georgia (Schröter et al. 2015) and even from Moscow (Onishko 2022) and may actually be the typical European version of E. c. cyathigerum (see Benedek 1968: fig. 6). ...
... 2c), that E. cyathigerum var. rotundatum Bartenef, 1929 is a senior subjective synonym of E. risi Schmidt, 1961(Kosterin 2004Kosterin & Zaika 2010;2011;Schröter et al. 2015;Onish ko & Kosterin 2021;Boudot et al. 2021). The taxon risi used to be regarded to occupy open, semiarid to arid territories from the Volga River in the west to East Siberia and Mongolia in the east and Iran and Afghanistan in the south, and being replaced by E. cyathigerum s. str. in Western and Central Europe, Asia Minor and the forest zone of Asia. ...
... From this point of view until recently it looked unnatural for the taxon risi to inhabit peat-moss lakes surrounded by beech forest in moist and cool highlands of the West Caucasus, such as the type locality of E. cyathigerum var. rotundatum (Schröter et al. 2015). Therefore, before the topotype of the latter was analysed, it would be reasonable to suggest that its type series, or just the holotype, were represented by somewhat ab-errant specimen(s). ...
Article
Enallagma cyathigerum var. rotundatum Bartenef, 1929, Leucorrhinia circassica Bartenef, 1929, and Aeschna juncea var. atshischgho Bartenef, 1929, were described by A.N. Bartenev (= Bartenef) in three papers published in 1929 and 1930. Their type locality was the same highland lake group near Krasnaya Polyana Town in West Caucasus, Russia, presently known as the Khmelevskie Lakes. Their type series most probably no longer exist. Topotypes of the two former taxa obtained in 2008 and 2013, respectively, were examined as well as a specimen supposedly of the third taxon, collected 36 km from the type locality. Based on these specimens, E. cyathigerum rotundatum is concluded to be a valid subspecies and the senior subjective synonym of Enallagma risi Schmidt, 1961, and L. circassica to be a junior subjective synonym of Leucorrhinia dubia (Vander Linden, 1825). The status of A. juncea atshischgho remains unresolved. Re-evaluation of available knowledge of the Palaearctic Enallagma spp. suggested downgrading Enallagma deserti (Selys, 1879) to the subspecies, E. cyathigerum deserti.
... Evidence of this has been provided for S. nigra in various regions (Boudot et al. 2009;Schröter et al. 2015;Lohr 2021). The fact that Trithemis annulata was only recorded in three localities (6, 8, and 9) confirms that the species must have been quite rare in northern Morocco at that time (Lieftinck 1966;Dumont 1972). ...
Article
Full-text available
Odonata collected by Antoine Senglet in Morocco from 12.vi. to 13.vii.1967 in 28 localities are deposited in the Muséum d’histoire naturelle in Geneva (MHNG, Switzerland). The collection includes 453 imagines of 46 species and 326 exuviae of 24 species, corresponding to 73 % of the presently known Moroccan Odonata fauna. It is one of the largest collections of Odonata ever made in Morocco and includes the first known evidence for Erythromma viridulum, Orthetrum brunneum, O. cancellatum, Selysiothemis nigra, and Sympetrum sinaiticum for Morocco. Reproduction is proven by the presence of exuviae for all these species except E. viridulum. The collection, which has remained undocumented for more than half a century, is comparable in scope to the contributions presented by the first two syntheses on the dragonflies of Morocco published by Lieftinck (1966) and Dumont (1972). A chronological check-list of the odonate fauna of Morocco details the increase in knowledge from 1850 to the present day.
... The 'taxa' considered by Schmidt can be no more than morphological morphs and the current authors do not recognise subspecies in I. elegans (e.g. Boudot & Salamun 2015;Schröter et al. 2015;Schneider et al. 2018;Kosterin & Ahmadi 2018). At the same time, I. e. marquardti hardly received any attention after Schmidt (1938;1967). ...
... Diagnosis. While currently I. elegans is considered as a monotypical species (Boudot & Salamun 2015;Schröter et al. 2015;Schneider et al. 2018;Kosterin & Ahmadi 2018), a new subspecies described for it should be compared to the nominotypical subspecies which is to be redefined. Its type locality is Europe, from where the species was described. ...
... These Iranian specimens can hardly be attributed to I. e. elegans. The intra-specific taxonomy of I. elegans was worked out by Schmidt (1967) but in a conceptually inconsistent way (see 'Introduction'; Boudot & Salamun 2015;Schröter et al. 2015;Kosterin & Ahmadi 2018). According to Schmidt (1967), Iran is inhabited by three subspecies of I. elegans (I. ...
Article
Ischnura elegans malikovae ssp. n. is described from the southern Far East of Russia (type locality: Russia, Primorskiy Kray, Pozharskiy District, Luchegorsk Town, the Luchegorsk Reservoir). Reconsideration of literature suggested it to broadly range in East Asia including Korea, Japan (Hokkaido and northernmost Honshu), north and north-east China and to be hitherto mistaken for Ischnura elegans elegans (Vander Linden, 1820) in Japan. The main difference of the new subspecies from I. e. elegans is the male paraprocts that are about 1.5 times shorter and scarcely divaricating in dorsal view and directed obliquely upward in lateral view. Ischnura elegans ebneri Schmidt, 1938 is reconsidered as the presumably Anterior Asian subspecies characterised by scarcely or not diverging male paraprocts in dorsal view, versus strongly diverging in I. e. elegans. Based on scarce information in the literature, I. elegans marquardti Schmidt, 1938 is supposed to be a junior synonym of I. elegans ordosi Bartenev, 1912 stat. rev., which is suggested to be an eastern Central Asian subspecies characterised by an incised prothoracic process in males.
... Selys, 1854Synonyms: Onigogomphus Brauner, 1902Paragomphus Cowley, 1934 Onychogomphus flexuosus Schneider, 1845 Synonym: Gomphus flexuosus Schneider, 1845 Material examined: 2 adult specimens; Thi-Qar Province, Al-Chibayish Marshes, 27.viii.2020. Distribution: Iraq (Morton, 1919 and listed from marshes (Garstecki and Amr, 2011); Palestine (Morton, 1924); Caucasus (Zazanashvili and Mallon, 2009); Georgia (Schroter et al., 2015); Turkey (Salur and Özsaraç, 2004); Armenia (Ananain and Tailly, 2013); This species distributed from Anatolia and Jordan Valley to Tajikistan and Afghanistan (Kakman et al., 2009). ...
Article
Full-text available
This study included a survey and review of the scientific names of the marsh insects (aquatic and surrounding it) for the purpose of unifying and updating the database. The survey reveals 109 species under 77 genera that belong to 32 families and 7 orders as follow: Coleoptera (44 species), Diptera (7 species) Ephemeroptera (2 species), Hemiptera (14 species), Hymenoptera (11 species), Lepidoptera (2 species) and Odonata with 29 species. Information of specimens' collection for each species, synonyms and geographical distribution were provided.
... C. heros is known from rather Central and Southeast Europe, reaching Ukraine in the North-East [65]. C. picta inhabits an area extending from North-Eastern Greece and Bulgaria, through West and North Turkey, including Samos and Lesbos in the Aegean, along the Black Sea coast as far as Russia, Georgia and Azerbaijan [16,66,67]. However, the presence of C. picta in Azerbaijan may be questioned, as the only voucher specimen is old and in bad condition; it is not clear whether it belongs to C. picta, to C. vanbrinkae or is a hybrid between them [16]. ...
... C. heros is known from rather Central and Southeast Europe, reaching Ukraine in the North-East [65]. C. picta inhabits an area extending from North-Eastern Greece and Bulgaria, through West and North Turkey, including Samos and Lesbos in the Aegean, along the Black Sea coast as far as Russia, Georgia and Azerbaijan [16,66,67]. However, the presence of C. picta in Azerbaijan may be questioned, as the only voucher specimen is old and in bad condition; it is not clear whether it belongs to C. picta, to C. vanbrinkae or is a hybrid between them [16]. ...
Article
Full-text available
Taxonomy of the genus Cordulegaster Leach in Brewster, 1815 in the Eastern part of the Western Palaearctic is poorly resolved. A two-step approach was applied: sequences of mitochondrial and nuclear DNA fragments were used to sort specimens; poorly known or new taxa with their phenotypic variation were described. The existence of two traditional groups (boltonii- and bidentata-group) was confirmed. Cordulegaster coronata Morton, 1916, however, belongs to a different group. Molecular-analysis supported three known and one new species (C. heros Theischinger, 1979, C. picta Selys, 1854, C. vanbrinkae Lohmann, 1993, and C. kalkmani sp. nov.) in the boltonii-group. In the bidentata-group, all specimens from West-Turkey belonged to C. insignis Schneider, 1845, all specimens further east to a complex of four closely related species, which we name charpentieri-complex (C. amasina Morton, 1916, stat. rev., C. mzymtae Bartenev, 1929 C. charpentieri (Kolenati, 1846), stat. rev. and C. cilicia sp. nov.). The following taxa: C. insignis nobilis Morton, 1916, syn. nov., C. nachitschevanica Skvortsov and Snegovaya, 2015, syn. nov. C. plagionyx Skvortsov and Snegovaya, 2015, syn. nov. and the Caucasian subspecies C. insignis lagodechica Bartenev, 1930, syn. nov., were synonymized with C. charpentieri. Finally, we provide a key for all Western Palaearctic Cordulegaster.
... Notes. For taxonomic status of the eastern representatives of L. virens see Schröter et al. [2015]. ...
... Notes. The current consensus is absence of clear subspecies in I. elegans [Schröter et al., 2015;Kosterin, Ahmadi, 2018;Schneider et al., 2018;Malikova, Kosterin, 2019]. ...