Research Article |
Corresponding author: Jan Šumpich ( jansumpich@seznam.cz ) Academic editor: Théo Léger
© 2022 Jan Šumpich, Ole Karsholt, Nikolay Savenkov, Hartmut Roweck.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Šumpich J, Karsholt O, Savenkov N, Roweck H (2022) The genus Tegostoma in Armenia, with description of a new species (Crambidae, Odontiinae). Nota Lepidopterologica 45: 269-278. https://doi.org/10.3897/nl.45.87795
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A small but beautifully coloured species of Tegostoma Zeller, 1847, which was collected by the authors in Armenia, has turned out to be unnamed and is here described as Tegostoma burtoni sp. nov. The description is supported by morphology and DNA barcodes . Photographs of the adults and genitalia of both sexes are provided. Tegostoma lepidalis (Herrich-Schäffer, 1851) and Pyrausta gulpembe Kemal & Koçak, 2018 are recorded as new species for Armenia.
The genus Tegostoma Zeller, 1847 comprises 31 species (
The aim of this contribution is to present the description of a new species, which is very conspicuous by its external appearance. Apart from consulting relevant literature, we have continuously searched for this species in various museum collections, including the museums in Vienna, Berlin and St Petersburg, wrich in Lepidoptera from Armenia, and where it would be easily recognizable due to its striking colouration. As a result, we came to the conclusion that this is a hitherto undescribed species, the description of which we present here.
The study material collected was attracted at ultraviolet light (8W/12V tubes and 80W mercury vapour bulbs) installed in portable light traps.
Tissue samples (dry legs) from specimens of Tegostoma and Pyrausta gulpembe were successfully processed at the Canadian Centre for DNA Barcoding (CCBG, Biodiversity Institute of Ontario, University of Guelph) (
The pinned specimens were photographed with a Canon 750D camera and a Canon MP-E-65 mm lens. Genitalia preparations were photographed with a Canon EOS 200D camera mounted on an Olympus CX31 stereomicroscope.
The descriptions of the genitalia and the descriptions of the wing patterns are based on the terminology in
ECKU Collection of Ecology-Centre, Kiel University, Germany
LNMNH Latvian National Museum of Natural History
NRC Collection of Nature Research Center, Vilnius, Lithuania
ZMUC Zoological Museum, Natural History Museum of Denmark, Copenhagen, Denmark
Type material. Holotype ♂: Armenia mer., Vedi env., Goravan vill., Gorovan Sands, 956 m, 39°53'20"N, 44°43'58"E, sandy steppe, 31.v.2017 (Barcode
Tegostoma burtoni sp. nov. is similar to some other Tegostoma species, mainly T. lepidalis (Herrich-Schäffer, 1851), and to Pyrausta gulpembe Kemal & Koçak, 2018 in external appereance, but it differs by its smaller wingspan. It differs from all Tegostoma species of comparable size by the distinctive purple colour of the forewings.
External appearance
(Figs
Variation. Sexual dimorphism not observed, it seems females differ in smaller size and less pronounced light fascia. The ground colour of most specimens is pinkish to purple, however, this is less pronounced in some specimens. Both fasciae are always paler compared with the ground colour but in some specimens they can be yellowish-buff, not pinkish. Specimens with a pinkish streak usually do not have a pale marginal line.
Male genitalia. (Figs
Female genitalia
(Figs
apophyses posteriores short, 2/3 the length of the apophyses anteriores. Ostium bursae broad, membranous. Antrum narrow, sclerotised, in the shape of a coiled leaf. Ductus bursae comparatively narrow, membranous, continuously gradually expanding anteriorly, and eventually becoming the bursa copulatrix, which is an elongate ovoid, membranous, without signa.
Female genitalia and male abdomen of Tegostoma burtoni sp. nov. 10. General view of the female genitalia; 11. Detail of ostium area (different view of the same genitalia slide, photographed before being removed from the abdomen), enlarged; 12. Male abdomen (open view). Scale bar: 1 mm.
BIN: BOLD:AEL8899 (n = 2). The intraspecific average distance of the barcode region is 0.0% (n = 2). The minimum distance to the nearest neighbour, Tegostoma lepidalis, is 3.24% (Fig.
Armenia.
The new species was collected in sandy habitats with sparse vegetation at an altitude of about 1000 m (Fig.
The species name is derived from the name of John Andrew Burton, a worldwide active conservationist, in honour of his strong support of establishing nature reserves in Armenia. It is to his merit to have established the Artsakh Nature fund and that more than 30,000 hectares of unique habitats are now protected within the borders of the Caucasus Wildlife Refuge.
The nature reserve is named after the old name of the village Gorovan, which has later become Goravan. But the official name of this protected area remained in its original spelling. Therefore, the names of the municipality and the protected area differ.
The National Sanctuary Gorovan Sands was established in 1959 in order to protect the habitats for endangered animals, as well as the site conditions with their unique vegetation. One of the most typical ecosystems of the arid zone are sandy Artemisia semi-deserts with a fauna and flora well adapted to extreme drought and temperature variation. Gorovan Sands Sanctuary, with roughly 175 (originally ca 200) ha, represents the largest of this type in the whole of Armenia. Like other deserts of this type it is dominated by cold winters, dry and hot summer months and an annual precipitaion of just 200–300 mm.
The vegetation is dominated by tussocks of Artemisia fragans, Achillea tenuifolia, saltresistant plants such as Salsola ssp., Kochia prostrata, Ziziphora tenuior, Calligonum polygonoides) and other, mainly psammophytic plant species, which show a huge variety of adaptation to sandy site conditions with a poor supply of nutrients and extreme dry periods, mixed with a wider spread of generalist species of cultivation (such as the locally dominant Lepidium vesicarium). About 160 species of vascular plants have been recorded (
Besides overgrazing and a rather intensive collecting of edible plants by local people, even more important for the future of this sanctuary is to keep reclamation, sand and travertine mining, dumping, and offroad driving within boundaries and thus allow processes of regeneration on the remainder of the site.
Tegostoma albizonalis Hampson, 1900
Distribution. Armenia, Turkmenistan (
Remarks. Part of type series originated from Armenia.
Tegostoma burtoni sp. nov.
Material examined. (see above).
Distribution. Armenia (this paper).
Tegostoma comparalis (Hübner, 1796)
Material examined. Armenia, Gorovan Sands, 910 m, 39°53'35"N, 44°43'03"E, 4 ♂, 2 ♀, 25.–27.v.2019, O. Karsholt & N. Savenkov; prov. Ararat, Urtsadzor, Caucasus Wildlife Reserve, Eco Lodge, 1250 m, 39°56'58"N, 44°53'14"E, 1 ♂, 22.–30.v.2019, O. Karsholt, H. Roweck, & N. Savenkov leg. (ZMUC).
Distribution. Southern Europe (
Tegostoma disparalis (Herrich-Schäffer, [1855])
Material examined. Armenia, Gorovan Sands, 910 m, 39°53'35"N, 44°43'03"E, 5 ♂, 1 ♀, 25.–27.v.2019, O. Karsholt & N. Savenkov (ZMUC).
Distribution. Turkey (
Tegostoma lepidalis (Herrich-Schäffer, 1851)
Fig.
Material examined. Armenia, Ararat Province, National Park of Khosrov, Vedi River Valley, 1298 m., 9.vi.2015, 1 ♂, 1 ♀ (barcode data
Distribution. Turkey (Herrich-Schäffer 1851), Iran (
Tegostoma ruptilineale Zerny, 1914
Distribution. Armenia (
Remarks. The species was described from Armenia.
Pyrausta gulpembe Kemal & Koçak, 2018
Fig.
Material examined. Armenia, Areni env., Noravank monastery, 2.vi.2017 (Barcode
Molecular data. BIN: BOLD:AEG0940. The intraspecific average distance of the barcode region is 0.48% (n = 2). The minimum distance to the nearest neighbour, unidentified Evergestis Hübner, [1825] from Iran (BOLD:AAH6764), is 5.61% (p-dist).
Distribution. Turkey (
We thank Alois Pavlíčko (Prague, Czech Republic) for providing a photograph of the sandy habitat of the new species and Povilas Ivinskis, Nature Research Center (Vilnius, Lithuania) for providing his faunistic records. Flemming Vilhelmsen, ZMUC is thanked for helpful information. The field investigations were conducted in collaboration with Scientific Center of Zoology and Hydroecology (National Academy of Sciences of Armenia). We also thank Ruben Khachatryan (Director of the Armenian Foundation for the Preservation of Wildlife and Cultural Assets) and Mark Kalashian (Scientific Center of Zoology and Hydroecology, Yerevan, Armenia) for their strong support of our field work. The first author expresses his gratitude to Gayane Karagyan (Scientific Center of Zoology and Hydroecology, Yerevan, Armenia) for his company during the trip to Armenia and for the direction to the important Armenian sites. We are grateful to Stella D. Beavan (Zeal Monachorum, UK) and Robert J. (Bob) Heckford (Plymouth, UK) who improved the English language and provided many useful comments to the text. We also thank reviewer Richard Mally for helpful comments and editor Théo Léger for careful review of the text. J. Šumpich carried out his part of the work on this article with support from the Ministry of Culture Czech Republic (DKRVO 2019–2023 / 5.I.d, National Museum, 00023272).