Research Article |
Corresponding author: Sarah Ehlers ( sarah.ehlers@mfn.berlin ) Academic editor: Ulrike Aspöck
© 2024 Sarah Ehlers, Hongyu Li, Lukas Kirschey, Michael Ohl.
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:
Ehlers S, Li H, Kirschey L, Ohl M (2024) A new species of the mantidfly genus Euclimacia from Vietnam (Neuroptera, Mantispidae). Deutsche Entomologische Zeitschrift 71(2): 255-264. https://doi.org/10.3897/dez.71.123553
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A new species of the family Mantispidae (Neuroptera) from Vietnam is described. Euclimacia radioquaesentis sp. nov. shows a unique colour pattern, which is distinctive within the genus. The colouration and morphology of both sexes of the new species are described in detail and illustrated. The naming of the new species is linked to a popular citizen-science event in choosing the name for this species (and three other species from different undescribed species by taxonomists of the Museum für Naturkunde Berlin).
Adaption, lacewings, mimicry, new species, parasitoid, polymorphism, sexual dimorphism, Southeast Asia, wasp mimic
The Mantispidae is a family within the holometabolous order Neuroptera, which has a remarkable morphology and interesting, but so far scarcely studied biology. The larvae of the subfamily Mantispinae are predatory and feeding on spider eggs (
Adult mantispids are characterised by a triangular head, raptorial forelegs and an elongated tubular prothorax, which makes them appear very similar to mantids (
Formerly, this family was assumed to be monophyletic, with its extant members classified into four subfamilies: Mantispinae, Calomantispinae, Symphrasinae and Drepanicinae (e.g.
Euclimacia Enderlein, 1910 belongs to the most diverse subfamily Mantispinae, which comprises of 320 species in 35 genera (
Overview of the currently valid Euclimacia species and their known distribution.
Species | Distribution |
---|---|
Euclimacia badia Okamoto, 1910 | Taiwan, Japan |
Euclimacia basiflava Handschin, 1961 | Malaysia |
Euclimacia burmanella (Westwood, 1867) | Myanmar |
Euclimacia celebica Handschin, 1961 | Indonesia (Sulawesi) |
Euclimacia cottami Navás, 1914 | India (Sikkim) |
Euclimacia flavicauda Esben-Petersen, 1917 | Indonesia (Sumatra) |
Euclimacia flavocincta Stitz, 1913 | Solomon Islands |
Euclimacia fusca Stitz, 1913 | Taiwan, Japan |
Euclimacia gerstaeckeri Banks, 1920 | Singapore, Malaysia |
Euclimacia grandis (Guérin-Méneville, 1831) | Indonesia (Ambon) |
Euclimacia horstaspoecki Ohl, 2004 | Thailand |
Euclimacia jacobsoni Handschin, 1961 | Indonesia (Sumatra) |
Euclimacia metallica Esben-Petersen, 1917 | Indonesia (Sulawesi, Sumatra) |
Euclimacia morosa (Gerstaecker, 1893) | Borneo, Philippines (Palawan) |
Euclimacia nelsoni Navás, 1914 | Sri Lanka |
Euclimacia nicobarica Kaur, 2021 | India (Andaman Islands, Nicobar Islands) |
Euclimacia nigra Handschin, 1961 | Indonesia (Java) |
Euclimacia nodosa (Westwood, 1847) | India (Assam) |
Euclimacia nuchalis (Gerstaecker, 1985) | Australia (New South Wales, Northern Territory, Queensland). |
Euclimacia partita Enderlein, 1910 | Indonesia (Sulawesi) |
Euclimacia radioquaesentis Ehlers, sp. nov. | Vietnam |
Euclimacia regina Esben-Petersen, 1917 | Indonesia (Java, Sunda Islands), Singapore |
Euclimacia rhombica Navás, 1914 | Myanmar |
Euclimacia rufa Esben-Peterson, 1928 | Indonesia (Sumatra) |
Euclimacia ruficauda Enderlein, 1910 | Indonesia (Sulawesi) |
Euclimacia rufocincta Handschin, 1961 | Borneo |
Euclimacia similis Kaur, 2021 | India (Madhya Pradesh) |
Euclimacia superba Lambkin, 1987 | Australia (Queensland) |
Euclimacia tagalensis Banks, 1914 | Philippines (Luzon) |
Euclimacia torquata Navás, 1914 | Australia (New South Wales, Queensland), New Guinea |
Euclimacia triangularis Handschin, 1961 | Philippines |
Euclimacia vespiformis Okamoto, 1910 | Taiwan, Japan |
Euclimacia woodhousei Navás, 1914 | India (Sikkim) |
Euclimacia zonalis Navás, 1914 | Indonesia (Sulawesi) |
In the present study, we describe a new species from Vietnam (Fig.
Euclimacia radioquaesentis sp. nov. male holotype and female paratype with distribution map. A. Habitus dorsal holotype male. Insert shows asymmetrical bifurcation between left and right costal area of fore-wings. Antecostal sutures (acs) and glabrous marks (gm) visible. The two black lines on the margin of the wing apex of the right fore-wing indicate the width of the oblique apical dark band; B. Localities (red rhombus) in Vietnam of the radioquaesentis type series. The number in the rhombus symbol indicates the count of specimens in this locality; C. Female paratype radioquaesentis dorsal view. The two black lines on the margin of the wing apex of the right fore-wing indicate the width of the oblique apical dark band. Scale bars: 5 mm (A, B).
The type series is part of the large collection of Southeast Asian Mantispidae deposited in the Royal Belgium Institute of Natural Sciences, Brussels, Belgium. One paratype is housed in the collections of the Museum für Naturkunde, Berlin, Germany.
The genital preparation was made from one paratype. Punctures were made in the area of the fourth abdominal segment with the aid of an insect pin size 0. Polyethylene foam was cut into required pieces, which were attached to the pinned specimen with needles to stabilise it for the preparation. The abdomen was very carefully perforated all around until the posterior part could be detached by a gentle levering action of the needle. The dissected abdominal end was left in 15% potassium hydroxide solution for approx. 21 h, then rinsed with distilled water and transferred to glycerol.
Images were taken with a Sony a7rIII and a Sony Makro G OSS 90mm f 2.8 lens for the habitus and a Canon MP-E 65mm f 2.8 lens for the details. Multi-focus imaging was facilitated by a Novoflex Castel-Mikro stepping motor-controlled focusing rack. To take the images, the software Capture One was used. For stacking, the software Helicon Focus was used. Genital images were made with a Leica Z16 APO A motorised macroscope with a Leica DFC camera. Measurements were done with Fiji (ImageJ) Version 2.1.0/1.53c.
Photos were post-processed with Adobe Photoshop version CC 2019 an arranged and labelled with Adobe InDesign version 19.2.
Illustrations were made with Adobe Illustrator version 25.0.
Distribution map was generated with QGIS version 3.16 Hannover, Natural Earth Data and Adobe Photoshop version CC 2019.
The terminology is based on
Order Neuroptera Linnaeus, 1758
Family Mantispidae Leach, 1815
Subfamily Mantispinae Leach, 1815
Euclimacia partita Enderlein, 1910: 366, by original designation.
The species epithet is made up of two words ‘radio’ and ‘quaesentis’. The latter derives from Latin and means ‘searched for’. The name was chosen as part of a radio show. Citizens were invited to submit name suggestions. The most suitable was radioquaesentis – searched for on the radio.
Holotype. Vietnam • ♂; Quang Tri, Huong Hoa Nature Reserve; 16°56'15''N, 106°34'52''E; 400 m; 7–10 Nov. 2007; G. Csorba leg., T. S. Nguyen leg., D. T. Pham leg., T. T. Nguyen leg., X. N. Nguyen leg.; light trap; CSOVI – Vietnam No. 92; coll.mfn-berlin.de_u_8bfa03; ISNB.
Paratypes. Vietnam • 4 ♂; Quang Tri, Huong Hoa Nature Reserve; 16°56'15''N, 106°34'52''E; 400 m; 7–10 Nov. 2007; G. Csorba leg., T. S. Nguyen leg., D. T. Pham leg., T. T. Nguyen leg., X. N. Nguyen leg.; light trap; CSOVI – Vietnam No. 92; coll.mfn-berlin.de_u_7e303d, coll.mfn-berlin.de_u_29a944, coll.mfn-berlin.de_u_199711, coll.mfn-berlin.de_u_93bd60; ISNB • 1 ♂; same collection data as for preceding; coll.mfn-berlin.de_u_5ea2b5; ZBM • 1 ♂; Gia Lai, Kon Chu Rang Nature Reserve; 14°28'28"N, 108°32'27''E; 1200 m; 13–20 Jul. 2018; J. Constant leg., J. Bresseel leg., X. Vermeersch leg.; GTI Project, I.G.: 33.769; coll.mfn-berlin.de_u_6c2cbd; ISNB • 1 ♀; Ninh Bình, Cuc Phuong National Park; 11–18 Jul. 2010; J. Constant leg., P. Limbourg leg.; ISNB.
The combination of colour characters in the new species is unique within Euclimacia. The contrast between the head and prothorax and the rest of the thorax and abdomen is striking. The prothorax and head have a distinct yellow colour, the remaining thorax is almost uniformly black. The abdomen of the male is also almost completely black with only a few brown markings. The female has a brownish abdomen with a black base. The wing colour is also unique in combination with the body colouration. The wings of E radioquaesentis have the prominent feature of differently-coloured pterostigmata in fore and hind wing. Whereas the fore-wing pterostigma is yellow, the hind-wing pterostigma is brown. There are currently six species in Euclimacia with this diagnostic character, but these species differ distinctly in body colouration. Whereas in E. radioquaesentis sp. nov., the head and the prothorax are markedly yellow, in the other six species both parts are either ferruginous (E. rhombica Navás, 1914), reddish-brown (E. morosa (Gerstäcker, 1893); E. zonalis Navás, 1914; E. regina Esben-Petersen, 1917; E. rufocincta Handschin, 1961) or completely black (E. gerstaeckeri Banks, 1920).
Measurements and ratios [in mm]. The given size range of each defined measurement area comprises minimum and maximum measured values of all seven specimens: Minimum frontal eye distance [WBE]: male 1.32–1.56; female 1.05. Maximum frontal head width including eyes [WAE]: male 3.96–4.44; female 3.25. Pronatal length, measured lateral from the anterior margin of the prozona to the dorsal basis of the prothorax [PL]: male 3.6–4.53; female 3.6. Pronatal width at maculae [WAM]: male 1.92–2.41; female 1.5. Pronatal ratio (length: width) [PL: WAM]: male 1.81–2.03; female 2.4. Maximum fore femoral length [LFF]: male 6.42–7.39; female 5.44. Maximum fore femoral width [WFF]: male 21–2.52; female 1.6. Fore femoral ratio (length: width) [LFF: WFF]: male 2.55–3.52; female 3.4. Maximum hind femoral length [LHF]: male 4.61–5.46; female 3.85. Hind femoral ratio (Hind femoral length: head width including eyes) [LHF: WAE]: male 1.08–1.38; female 1.18. Fore-wing length (measured at the middle of the humeral plate to the outer apex of the wing) [LFW]: male 22.21–25.1; female 17. Fore-wing width (measured down from the base of the pterostigma at a right angle) [WFW]: male 4.8–5.1; female 4.08. Fore-wing ratio (length: width) [LFW: WFW]: male 4.48–4.95; female 4.15. Maximum length of fore-wing anterior radial cell II [Lrarp2]: male 4.19–5.2; female 3.02. Maximum width of fore-wing anterior radial cell II [Wrarp2]: male 0.46–0.57; female 0.45. Fore-wing 2R1 ratio (length: width) [L2R1: W2R1]: male 8.6–10.57; female 6.71. Maximum hind-wing length (measured at the middle of the humeral plate to the outer apex of the wing): male 19.57–21.9; female 15.55. Maximum hind-wing width (measured down from the base of the pterostigma at a right angle): male 4.26–5.1; female 3.62. Hind-wing ratio (length: width): male 4.29–4.69; female 4.3.
Head. Holotype: Left antenna with 47 flagellomeres, right with 46 flagellomeres. Antennae of male paratypes ranging from 42 to 47 flagellomeres, left and right antennae with different number of flagellomeres in all specimens. Female: 41 flagellomeres right, left antennae missing.
Frons approximately square-shaped basically with outwardly curved lateral subantennal sutures (Fig.
Euclimacia radioquaesentis male. A. Head frontal view. The subantennal suture (sas) is curved outwards; B. Head and thorax in dorsal view. The epicranial sutures are comprised by the frontal sutures (fs) and the coronal suture (cs). A black transversal band runs along the pronatal groove over the maculae (mc) and the pronatal humps (ph). The horizontal dashed lines indicate the three areas of the prothorax, the prozona (p1), the metazona (p2) and the pronatal base (p3); C. Lateral view on head, thorax and forelegs. Scale bars: 1 mm (A); 2 mm (B, C).
Prothorax.
Pronatal humps distinctly protruding (Fig.
Euclimacia radioquaesentis prothorax of both sexes in lateral view. A. Male. Pronatal hump (white arrowhead) distinctly protruding. The black marking on the pronatal hump and the black marking on the macula are connected; B. Female. Pronatal hump (white arrowhead) barely protrudes. Dark marking on pronatal hump faintly present and not interfering with the black mark of the macula. Scale bars: 5 mm (A, B).
Wings.
Number of subcostal veinlets and their bifurcations are asymmetric. Holotype: Left fore-wing costal space proximal to pterostigma with 17 subcostal veinlets, first (most proximal) subcostal veinlet counted as one, but with bifurcation in anterior direction (Fig.
Abdomen.
Abdominal segments with indistinct pilosity, dull appearance, without enlarged membranes or pores (Fig.
Euclimacia radioquaesentis male terminalia and inner genitals. A. Dorsal view of abdominal segment VII–IX; B. Illustration of the inner genitals from dorsal view with same orientation as in A; C. Male terminalia lateral view; D. Inner genitals from lateral view with same orientation as in C; E. Tergites IV–VI in lateral view. Abbreviations: cv, convex area; ect, ectoproct; gc, gonocoxite; hm, hypomere; m, membrane; pp, pseudopenis; s, sternite; t, tergite; vml, ventromedial lobus. Scale bars: 0.25 mm (A, B); 0.5 mm (C); 0.2 mm (D); 1 mm (E).
Tergite IX laterally about three times as wide as dorsally (Fig.
Female genetalia.
Gonocoxite VIII located between enlarged sternite VII and tergite VIII (Fig.
Euclimacia radioquaesentis female terminalia and inner genitals. A. Female terminalia lateral view; B. Spermatheca with bursa copulatrix lateral view; C. Terminalia ventral view; D. Spermatheca with bursa copulatrix ventral view. Abbreviations: b.c., bursa copulatrix; d.s., distal section of spermatheca; ect, ectoproct; fc, fertilisation canal; fcd, fertilisation canal duct; ga, gonapophysis; gc, gonocoxite; m.s., medial section of spermatheca; p.s., proximal section of spermatheca; d.s., distal section of spermatheca; s, sternite; t, tergite. Scale bars: 0.25 mm (A, B); 0.5 mm (C); 0.2 mm (D); 1 mm (E).
Head.
Yellowish with a slightly reddish tinge that contrasts with yellow colour of prozona (Figs
Euclimacia is a small, but morphologically markedly diverse genus. Despite the considerable size of individual specimens, which can reach sometimes up to 3 cm body length and their striking colouration in many cases, the number of specimens in scientific collections is very limited. So far, there is still no accurate information about their behaviour and their habitats during the day and at night. Euclimacia often represent a by-catch that is caught by scientists specialised in other taxa during light trapping. However, there is no evidence that they are nocturnal. Specific light trapping for Euclimacia has, so far, resulted in low numbers of specimens. It can be assumed that, similar to the genus Climaciella, during the day, they eat pollen and nectar on flowering plants and prey on other insects (
Of the 33 species described so far, 30 were described on the basis of a single specimen. The remaining two species were described, based on two (Euclimacia superba Lambkin, 1987) and three (Euclimacia nicobarica Kaur, 2021) specimens. The series of eight specimens of the here newly-described species Euclimacia radioquaesentis sp. nov. is thus comparatively large.
Seven males and one female of E. radioquaesentis were examined. The availability of both sexes provides rare data on potential sexual dimorphism in this genus. Only the descriptions of E. superba and E. nicobarica are based on both sexes. In E. nicobarica, the colour pattern of the female is described as similar to the male, although the female is slightly smaller than the male. In E. superba, there are a few differences in the colour pattern and size. The colour differences occur in slightly different colour shades and a few markings. The head of the female is slightly paler and it possesses a transverse band across the antennae basis, which is absent in the male. The female possesses a large dark transverse band on tergite III, the male in the same location possesses a small black median mark. In the female, the ectoproct is black-brown with a brownish-yellow spot. The ectoproct of the male is dark orange-brown without any spot. Wings and other body parts have the same colour. The female is slightly larger than the male. The size depends to a certain extent on the larvae’s food supply (size of the spider egg sac) and is, therefore, considered natural and not as a sexual trait (
In E. radioquaesentis, there are differences in colouration between females and males. One difference is the transversal band on the prothorax, which is present in both sexes, but reduced in the female. In the males, the pronatal hump is fully covered by a dark mark and this dark mark merges with the dark mark that covers the macula. The pronatal hump of the female has a very faint dark mark at the apex, which does not merge with the dark mark of the macula. In general, the prothorax of the female appears narrower and less wrinkled than of the male (Fig.
Furthermore, the abdomen of the male is predominantly black with a few brownish markings. The abdomen of the female has a significantly higher amount of brown, so that, apart from the anterior two black segments, the abdomen appears predominantly brown. The predisposition for this brown colouration of the abdomen is also present in the males, as the brown markings on the tergites indicate. The wings also differ, although only slightly, in colouration. The wings of the female appear more contrasting. The area along the posterior wing margin is darker than in the male and the oblique band above 3M in the fore-wing reaches the posterior wing margin. As a result, the hyaline median stripe is enhanced, especially in the fore-wing (Fig.
Intraspecific variation in Euclimacia has also been recorded only occasionally. There are observations of intraspecific variations in Euclimacia badia Okamoto, 1910.
Furthermore, the individuals differ slightly in size. Variation also occurs in the wing venation. There are variations between specimens, but also asymmetry within the same specimen. The asymmetry of subcostal veinlets within the wings of one specimen seems to be the norm.
Intraspecific variability within this genus is still difficult to assess and, in an ongoing revision, as much material as possible from this genus will be investigated. The trend indicates that there are species with hardly any intraspecific variability, as in the example of radioquaesentis and species with clear intraspecific variability, as in badia. Adaptation to morphologically different mimicry models (i.e. aculeate wasps) in different regions may result in intraspecific variability.
The description of E. radioquaesentis was linked to a popular science event of the Museum für Naturkunde Berlin and ‘Inforadio vom rbb’, one of Berlin’s local radio stations, in choosing the name for this species. Three more species from different taxa were also involved, the descriptions of two of which have already been published (a species of shrimp by
We thank the collectors of the specimens relevant to this species description in Huong Hoa Nature Reserve Vietnam (1 holotype, 4 paratypes): Truoung Sor. Nguyen, Duc Tien Pham, Thien Tao Nguyen, Xuan Nghia Nguyen and Gábor Csorba.
We thank the collectors of the sixth paratype in Kon Chu Rang Nature Reserve Vietnam: Jerome Constant, Joachim Bresseel and Xavier Vermeersch.
We thank the collectors of the seventh female paratype in Cuc Phuong National Park Vietnam: Jerome Constant and Pol Limbourg.
We gratefully acknowledge the Royal Belgium Institute of Natural Sciences, Brussels, Belgium for the loan of the specimens.