Research Article |
Corresponding author: Ana Grković ( ana.grkovic@dbe.uns.ac.rs ) Academic editor: Martin Hauser
© 2019 Ana Grković, John Smit, Snežana Radenković, Ante Vujić, Jeroen van Steenis.
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:
Grković A, Smit J, Radenković S, Vujić A, van Steenis J (2019) Two new European long-legged hoverfly species of the Eumerus binominatus species subgroup (Diptera, Syrphidae). ZooKeys 858: 91-108. https://doi.org/10.3897/zookeys.858.34663
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Eumerus Meigen (Diptera, Syrphidae) is one of the most speciose hoverfly genera in Europe, with several species groups recognized within. As part of the tricolor group of species, a subgroup of long-legged representatives stands out. We name it Eumerus binominatus subgroup and provide descriptions for two new European species which belong to this subgroup: E. grallator sp. nov. from mainland Spain and E. tenuitarsis sp. nov. from Lesvos and Evros, Greece. A key for all five recognized species of the binominatus subgroup is provided.
Binominatus subgroup, Eumerus, hoverflies, identification key, long-legged syrphids, tricolor group, Turano-Mediterranean distribution
The genus Eumerus Meigen (Merodontini) is one of the most species-rich hoverfly genera in the World. There are over 300 species known (
The members of Eumerus recorded in Southeast Europe belong to the following groups, identified on the basis of molecular markers in
In this paper we add yet another two European species to the list of tricolor group, one from the western Mediterranean and one from the eastern part of it. Both species belong to a species subgroup not previously recorded from the western Palearctic, characterized by slender elongated legs in the male, which is a unique feature within the family of Syrphidae, a long pilose thorax, pilose eyes and a stout abdomen. We included these species into the binominatus subgroup named after the Asian long-legged species E. binominatus Hervé-Bazin, 1923 (Fig.
The characters used in the key, descriptions, and drawings follow the terminology established by
The drawings and part of the figures were created using photographs taken with a Leica DFC 320 (Wetzlar, Germany) camera attached to a Leica MZ16 binocular stereomicroscope and then processed in Adobe Photoshop CS3 v10.0 (Adobe Systems, San Jose, CA, USA). The figures of Eumerus binominatus and E. tadzhikorum were created using photographs taken with a Canon EOS D6 equipped with a Canon MP-E 65 macro zoom lens. Several photos for each figure were processed with Zerene Stacker and further edited with the Photoshop program GIMP 2.8.22.
The distribution map was created in Adobe Illustrator CS6 V 16.0.0 software (Adobe Systems, San Jose, CA, USA).
The following acronyms for museums and entomological collections are used in the text:
AEPC A. van Eck private collection, Tilburg, The Netherlands
CEUA Colección Entomológica de la Universidad de Alicante, CIBIO-Alicante University, Spain
CSCA California State Collection of Arthropods, Sacramento, California, USA
DDPC D. Doczkal private collection, Malsch, Germany
SBPC S. Bot private collection, Haren, The Netherlands
Eyes densely whitish, pilose. Basoflagellomere relatively small, only about twice size of pedicel, oval to squarish in shape, with only a few short radial wrinkles. Male eyes holoptic or narrowly dichoptic. Abdomen short and stout (Fig.
The Eumerus binominatus subgroup shares all characters of the tricolor group (
E. selevini Stackelberg, 1949 is a middle-Asian species similar to the binominatus subgroup, based on the slender metafemur. The head of this species is very similar to that in E. binominatus and E. tadzhikorum but with smaller, equilateral ocellar triangle, placed medially on vertex, which is in the other two species large, elongated and placed closer to the upper eye margins. It differs by the normal shaped metatarsus, not elongated as in binominatus subgroup; elongate abdomen in comparison to the length of head and thorax together and with a characteristic lateral notch in the second metatarsal segment; the pilosity on the thorax is very short in E. selevini in contrast to species in the binominatus subgroup which makes this species easily recognizable.
The following species belong to the binominatus subgroup:
E. binominatus Hervé-Bazin, 1923 (Fig.
= E. maculipennis Becker, 1921 preocc. Bezzi, 1915
E. grallator sp. nov. (Fig.
E. longitarsis Peck, 1979
E. tenuitarsis sp. nov. (Fig.
E. tadzhikorum Stackelberg, 1949 (Fig.
This species was originally described by
Holotype ♂ Eumerus maculipennis Becker, 1921: “Transkaspien / 57442”, “maculipennis / Beck / det Becker”, “Holotypus” [red label], “Zool. Mus. / Berlin”, “Holotype ♂ / Eumerus maculipennis / Becker, 1921 / det. J. van Steenis, 2016, (
Male eyes separated by width of ocellus. Face black, covered in whitish pilosity with few black pilosities above antennae (Fig.
This species is similar to E. tadzhikorum but differentiated by the shape and color of the basoflagellomere.
Holotype. SPAIN ♂, Castilla la Mancha, Villahermosa. Original label: “España, Castilla / la Mancha, Villahermosa / [UTM] 30S WH19329-88405 / 23.vi.2003. 980 m / leg. J.T. Smit”. The holotype is in good condition with no apparent signs of wear, except for wingtips, which are both damaged. The holotype is deposited in the
Male. Ocellar triangle isosceles. Basoflagellomere blackish, small, rounded, with one or two short radial wrinkles. Constriction of elongated metafemur located in posterior half (Fig.
Eumerus grallator sp. nov., male A epandrium, lateral view B surstyle lobe, ventral view D medial part of hypandrium, lateral view G fourth sternum. Eumerus tenuitarsis sp. nov., male C hypandrium, lateral view E surstyle lobe, lateral view F epandrium, ventral view H fourth sternum. Abbreviations: c – cercus, dn – dorsal notch of hypandrium, in – interior accessory lobe of surstyle lobe, om – outer margin of posterior surstyle lobe in ventral view, ps – posterior lobe of surstylus, th – thecal ridge of hypandrium, vp – ventral protuberance of hypandrium. Scale bars: 0.2 mm (A–F); 0.5 mm (G, H).
Male. Body length (excluding antenna): 11.5 mm; wing length: 7 mm. Head. Eyes separated by the width of an ocellus and covered in dense white pilosity. Eye margins in anterior view almost parallel, slightly broadening ventrally. Face completely black pilose, covered in silver pollinosity, most expressed in middle. Frons, vertical triangle and occiput black; silver pollinosity well expressed along eye margin on frons, on vertex anteriorly and dorsally on occiput behind eye margin, but most distinctive laterally. Ocellar triangle isosceles and predominantly black pilose, becoming intermixed with white pile in front of ocellar triangle and turning predominantly white behind it. Distance from anterior to posterior ocellus same as distance from latter one to upper eye corner. Lower facial margin in lateral view not protruding. Scape and pedicel brown to black. Basoflagellomere dark brown, rounded and slightly longer than broad with one or two short radial wrinkles. Ventral pile of pedicel black, not longer than its depth. Thorax. Scutum and scutellum densely punctate, shiny, with a bluish tinge; covered in long dense white pilosity. Two vittae of white pollinosity on scutum faint and thin, hardly reaching base of wings. Pleurae black. Anepisternum entirely white pilose, except for some black pile just behind the anterior spiracle. Anepimeron white pilose with some black pile posteriorly. Katepisternum and katepimeron black pilose. Wing. Hyaline with pterostigma about same color as the wing. Vein R4+5 slightly curved. Wing covered in microtrichia except for basal cells mostly bare. Costal setae black. Halter blackish. Legs. Metaleg slender with all segments very elongated (Fig.
The specific epithet is the Latin word grallator meaning “one who walks on stilts”, which refers to the very slender and elongated legs of this species. It should be treated as a noun in apposition.
Spain.
The male holotype and one male paratype specimens were swept from a stand of some large yellow Apiaceae along a road, in an open park-like landscape of an oak dehesa. Accompanying hoverfly species were Eristalinus taeniops (Wiedemann, 1818), Eristalis arbustorum (Linnaeus, 1758), Eumerus barbarus (Coquebert, 1804), E. nudus Loew, 1848, Spilomyia digitata (Rondani, 1865) and Xanthogramma marginale (Loew, 1854).
This species was described from Tajikistan and is known from Asia Minor and south-central Asia. This species is likely to consist of a complex of closely related species in this region (Doczkal pers. comm.).
Holotype ♂ Eumerus longitarsis Peck, 1979: “Tajikistan, Hissar mountains / Takob ravine / Tian Shan h = 1700 m / leg. 23.vii.1976”, “399”, “Holotypus ♂ / Eumerus / longitarsis Peck” (
Additional material: “[Russia] So.[uthern] Primor’e [Primorsky Krai] / Kamenushka / A.Shatalkin [leg.]”, 1♂ (
Male. Ocellar triangle equilateral. Face with black pile. Constriction of the elongated metafemur is located in posterior half. Metatarsus remarkably longer than metatibia (Fig.
Described from Tajikistan and known from southern Kazakhstan, Kyrgyz, Tajikistan, Turkmenistan and Uzbekistan (
Holotype ♂ Eumerus tadzhikorum Stackelberg, 1949: “16.VI.[19]44”, “Eumerus typ. ’46 / tadzhikorum sp. nov. / Stackelberg det.”, ”Holotypus ’49 / Eumerus / tadzhikorum Stack.” [red label, partly handwritten], ”Lectotypus Eumerus / tadzhikorum Stack / design. V. Richter” [red label, partly handwritten], (
Additional material. Kazakhstan: “KZ Oblast Almaty / Tamgaly 886 m / lat 43.802 lng 75.534 / 8 V 2015 leg. S. Bot”, 1♂ (SBPC); “KAZAKHSTAN 29.V.2001 / SE Chilik 700m / 43°40'N 78°29'E / leg. M. Hauser”, 1♂ (CSCA). Armenia: “Мегри на р. Аракс / Армения / В. Рихтер” with added handwritten “2.5 km B. m. g. / стаиции / 7.V.974”, 1♂ (
Male. Eyes clearly separated by width of basoflagellomere. Wing with a dark spot (Fig.
This species is extremely similar to E. binominatus and it is possibly a subjective junior synonym of this species. The length of the setae on the apico-ventral side of the metafemur seems to vary in number and length. Due to lack of material no conclusion will be drawn here.
Holotype. GREECE • ♂, Lesvos, Agiassos. Original label: “Agiassos, 601 m / Lesbos, Greece / 39°4'16"N / 26°22'23"E / 23.vi.2003 / leg. M. Hull”. Paratype. GREECE • 1♀, Evros, Dadia, 26–28.vii.2013, 40,9943N 26.0933E leg. M. Kourtidou (
Male. Ocellar triangle isosceles (Fig.
Male. Body length (excluding antennae): 12 mm; wing length: 8 mm. Head. Eyes slightly dichoptic, separated by width of two ommatidia (Fig.
The species name is derived from the Latin words “tenui” and “tarsus” and refers to the extremely long and slender tarsi, especially obvious in the male metalegs.
Only known from the holotype and female paratype taken on Lesvos and Evros (Greece) respectively.
Current known distribution of the species of the Eumerus binominatus subgroup. Black dots stand for Eumerus grallator sp. nov., black triangle for Eumerus longitarsis Peck, 1979 Far East record only, black squares for E. tenuitarsis sp. nov. and grey area inferred distribution of Middle Asian species of the Eumerus binominatus subgroup, including E. binominatus, E. longitarsis and E. tadzhikorum.
Females of the subgroup are very difficult to distinguish morphologically. We have species with red abdomen from middle Asia which can be E. binominatus or E. tadzhikorum and black species which are in Spain E. grallator, in Greece E. tenuitarsis and in Middle Asia and Asia minor E. longitarsis. The distribution of E. tenuitarsis and E. longitarsis is not likely to be overlapping in Asia Minor and confusion between the female specimens of these species is not an issue.
1 | Basoflagellomere with more or less marked radially arranged wrinkles and clearly limited fossette. Katepisternum with medial pilosity connecting dorsal and ventral patch of pilosity. Anterior surstyle lobe of epandrium poorly developed | tricolor group, 2 |
– | Basoflagellomere not wrinkled radially with indistinctly expressed fossette. Katepisternum medially bare, with separated dorsal and ventral patch of pilosity. Anterior surstyle lobe of epandrium well developed | other Eumerus groups (not treated here) |
2 | Segments of metaleg extremely elongated, especially metatarsus as long as or longer than metafemur (Fig. |
binominatus subgroup, 3 |
– | Segments of metaleg not extremely elongated, metatarsus about 2/3–3/4 of length of metafemur | other Eumerus species from tricolor group (not treated here) |
3 | Terga with red markings laterally (Fig. |
4 |
– | Terga completely black (Fig. |
5 |
4 | Basoflagellomere brown-red and slightly higher than long (Fig. |
E. binominatus Hervé-Bazin |
– | Basoflagellomere black, as high as long (Fig. |
E. tadzhikorum Stackelberg |
5 | Greatest width of metafemur is approximately equal to one fifth of length of metafemur (Fig. |
6 |
– | Greatest width of metafemur is approximately equal to one eighth of length of metafemur (Fig. |
E. tenuitarsis sp. nov. |
6 | Metatarsus noticeably longer than metatibia and metafemur (Fig. |
E. longitarsis Peck |
– | Metatarsus approximately the equally long as metatibia and metafemur (Fig. |
E. grallator sp. nov. |
The Eumerus binominatus subgroup is a group of long-legged species sharing all diagnostic characters with E. tricolor group (
The remarkable long legs, especially conspicuous in males, could be behaviourally evolved or be part of a form of mimicry (
As shown here, the Turano-Mediterranean region represents a diversity center for the binominatus subgroup. The species of the binominatus subgroup are, however, not entirely restricted to this region given that we have one specimen of E. longitaris from the Russian Far East. This disjunct Turano-Mediterranean distribution is already recorded in several insect orders, in Acari and also in vipers (
We want to thank the following persons for their contribution to this study: Marina Janković (University of Novi Sad, Serbia) for constructive suggestions to the text; Theo Zeegers (Soest, the Netherlands) for providing a translation of Peck’s original description of Eumerus longitarsis (Peck, 1979); Dieter Doczkal (Münich, Germany) for the information regarding the Eumerus binominatus species group; André van Eck (Amsterdam, the Netherlands), Sander Bot (Haren, the Netherlands) and Antonio Ricarte (Alicante, Spain) are kindly thanked for the additional material and the information regarding this species. We thank Prof. Theodora Petanidou (University of the Aegean, Mytilene, Greece) for providing the female paratype of E. tenuitarsis sp. nov. within her collected material from Greece. The following curators are thanked for the possibility of studying specimens in their care: Olga Ovchinnikova and Nikolai Paramonov (St Petersburg, Russia) and Jenny Pohl (Berlin, Germany).
We thank subject Editor Martin Hauser (Sacramento, USA) for his valuable comments, suggestions and sharing his material from the subgroup studied here, during the editorial process which improved a lot a present manuscript.
Financial support for part of this research was provided by the Serbian Ministry of Education, Science and Technological Development (Projects OI173002 and III43002) and the Provincial Secretariat for Science and Technological Development (Project number 142-451-2591/2017). The last author received financial support through the Dutch Uyttenboogaart-Eliasen foundation under number SUB.2014.12.16 for the visit to the