Research Article |
Corresponding author: Galina N. Azarkina ( urmakuz@gmail.com ) Academic editor: Jeremy Miller
© 2015 Galina N. Azarkina, Marjan Komnenov.
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:
Azarkina GN, Komnenov M (2015) Descriptions of two new species of Aelurillus Simon, 1884 (Araneae, Salticidae) from the Mediterranean, with the synonymization of A. steliosi Dobroruka, 2002. ZooKeys 516: 109-122. https://doi.org/10.3897/zookeys.516.9439
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Two Aelurillus species are described as new, A. alboclypeus sp. n. (♂♀, from Turkey) and A. deltshevi sp. n. (♂, from Macedonia, Bulgaria and Azerbaijan). Aelurillus steliosi Dobroruka, 2002 is synonymized with A. leipoldae (Metzner, 1999). Additional distributions of the closely related species A. v-insignitus are provided for the region of study. Distributional maps are provided for the five species reported in this paper.
Aranei, jumping spiders, Mediterranean, synonymy
To date, 69 species and two subspecies of Aelurillus have been described in the world fauna (
This paper is based on both museum collections and newly collected material from Macedonia, Bulgaria, Greece and Turkey. Specimens were studied in ethanol and their colours refer to those of the preserved specimens. All drawings were made with the aid of a reticular eyepiece attached to an MBS-10 stereomicroscope. The male pedipalps and epigynes were detached for study. Epigynes were macerated in 20% KOH solution for one night. After being drawn, the copulatory organs were placed in microvials or small pieces of paper with ethanol together with the specimens from which they had been removed. Digital images were taken with a Zeiss Stemi 2000 and an attached Canon EOS 550D camera. Stack images were combined using Helicon Focus software. All drawings were edited and assembled in Adobe Photoshop. Distribution maps were produced using the online mapping software SimpleMappr (
Specimens for this study were borrowed from or placed in the following museums and personal collections:
ISEA Institute for Systematics and Ecology of Animals, Novosibirsk, Russia (G. N. Azarkina);
IZSB Institute of Zoology, Sofia, Bulgaria (C. Deltshev);
LM World Museums Liverpool, Liverpool, UK (G. Night);
MMUM Manchester Museum, University of Manchester, Manchester, UK (D.V. Logunov);
MNHN Muséum national d’Histoire naturelle, Paris, France (E.-A. Leguin);
NHM Natural History Museum, Vienna, Austria (J. Gruber);
NHMC Natural History Museum, University of Crete, Crete, Greece (A. Trichas);
PCHM Personal collection of H. Metzner (Burghaslach, Germany);
PCMK Personal collection of M. Komnenov (Scopje, Macedonia);
SMNK State Museum of Natural History, Karlsruhe (H.Höfer);
SNHM Senckenberg Natural History Museum, Frankfurt am Main, Germany (P. Jäger).
Abbreviations used in the text: AME – anterior median eyes, ALE – anterior lateral eyes, PLE – posterior lateral eyes, Fm – femur, Pt – patella, TA – terminal apophysis; Tb – tibia, Mt – metatarsus. The sequence of leg segments in measurement data is as follows: femur+patella+tibia+metatarsus+tarsus. All measurements are in mm. For the leg spination the system adopted is that used by
A. gershomi:
Holotype: ♂ (ISEA 000.287) TURKEY, Antalya Province, 18 km SSE of Elmali, Bey Mt. Range, 6 km WSW of Kızlarsivrisi Mt., 1800–2000 m a.s.l., 36°35'N, 30°03'E, 25 April 2009, coll. R.Yu. Dudko, I.I. Lyubechanskij, A.A. Stekolnikov. Paratypes: TURKEY: 1 ♂ (ISEA 000.286) Ankara Province, Bala District, Revnam Forests, 1392 m a.s.l., 39°40'N, 32°54'E, 29 May 2009, coll. Yu.M. Marusik; 1 ♂ 1 ♀ (ISEA 000.515) Çankırı Province, Ankara-Çankırı Highway, 689 m a.s.l., 40°23'N, 33°34'E, semidesert, 15 September 2010, coll. Yu.M. Marusik; 4 ♂ (ISEA 000.875) Adıyaman Province, Nemrut Mt., 37°58'N, 38°44'E, 14.05.1997 (V. Bryja); 1 ♂ (LM) Kayseri Province, Nigde, Demirkazık, 37°51'N, 35°05'E, 13 June 1993, coll. C. Felton; 1 ♂ (MNHN 12.840) Amasia [=Amasya], 40°39'N, 35°49'E, date unknown, coll. S.L.; 2 ♂ (NHM) Pass vor Alahan, Karaman ü. Mut [=Mersin Province, Alahan Monastery, nr Mut, 36°47'N, 33°21'E], 8 April 1977, coll. H. Nemenz.
This species is closely related to A. v-insignitus and other species of Aelurillus v-insignitus-group (sensu
The species is named for its “face coloration”: A. alboclypeus sp. n. has white dense hairs on the clypeus.
Male (holotype (small) and paratype (large) from Demirkazık ): Carapace 2.00–3.10 long, 1.60–2.10 wide, 1.00-1.80 high at PLE. Ocular area 0.95–1.10 long, 1.25–1.60 wide anteriorly and 1.20–1.55 wide posteriorly. Diameter of AME 0.30–0.40. Abdomen 1.90–2.50 long, 1.70–2.10 wide. Cheliceral length 0.65–1.00. Clypeal height 0.25–0.30. Length of leg segments: I 1.3+0.9+0.8+0.5+0.6; II 1.4+0.9+0.8+0.6+0.5; III 2.0+0.9+1.0+1.0+0.8; IV 1.9+0.9+1.2+1.5+0.8. Leg spination: I: Fm d 1–1–5; Pt pr 1; Tb pr 1–1–1, v 1–1–2 ap; Mt pr and rt 1–1, v 2–2 ap. II: Fm d 1–2–5; Pt pr and rt 1; Tb d 1–0–0, pr 1–1–1, v 1–1–2 ap; Mt pr and rt 1–1, v 2–2 ap. III: Fm d 1–3–5; Pt pr and rt 1; Tb d 1–0–0, pr and rt 1–1–1–1, v 1–0–2 ap; Mt d 1–1–0, pr and rt 1–0–2, v 1–1–2 ap. IV: Fm d 1–2–5; Pt pr and rt 1; Tb d 1–0–0, pr and rt 1–1–1–1, v 2–0–2 ap; Mt d 1–1–0, pr 1–1–2, rt 1–0–2, v 1–1–2 ap. Coloration. Carapace dark brown, with black eye field, covered with dark brown to black adpressed scales. Carapace with two thick white stripes dorsally (Fig.
Female (from Çankırı Prov.): Carapace 2.30 long, 1.30 wide, 1.20 high at PLE. Ocular area 1.00 long, 1.35 wide anteriorly and 1.30 wide posteriorly. Diameter of AME 0.40. Abdomen 2.20 long, 1.40 wide. Cheliceral length 0.70. Clypeal height 0.30. Length of leg segments: I 1.0+0.7+0.7+0.5+0.5; II 1.0+0.7+0.7+0.5+0.45; III 1.7+0.9+0.9+1.0+0.65; IV 1.55+0.7+0.85+1.2+0.7. Leg spination: I: Fm d 1–1–4; Tb pr 1–1, v 1–1–2 ap; Mt pr and rt 1–1, v 2–2 ap. II: Fm d 1–2–4; Tb pr 1–1, v 1–1–2 ap; Mt pr and rt 1–1, v 2–2 ap. III: Fm d 1–2–4; Pt pr and rt 1; Tb d 1–0–0, pr and rt 1–1–1, v 1–0–2 ap; Mt d 1–1–0, pr 1–0–2, rt 1–1–2, v 1–1–2 ap. IV: Fm d 1–1–2; Pt pr and rt 1; Tb d 1–0–0, pr and rt 1–1–1, v 2–0–2 ap; Mt d 1–1–0, pr 1–1–2, rt 1–0–2, v 1–1–2 ap. Coloration. Carapace dark brown with black ocular area, covered with white scales. Sternum dark brown covered with white hairs. Clypeus dark brown covered with white hairs, cheeks dark brown with two strips formatted by dense white hairs. Abdomen grayish-yellow, dorsum dark brown with mixed yellowish-white hair pattern. Book-lungs are grayish-yellow, spinnerets are yellowish-grey. All legs and palps are yellow. Legs with dark brown patches and semi-rings. Structure of spigyne and spermathecae as in Figs
Aelurillus alboclypeus sp. n.: 2 male, body pattern 3 left palp, ventral view 4 ditto, retrolateral view 5 male face 6 palpal femur, retrolateral view 7 embolic division, retrolateral view 8 ditto, dorsal view 9 ditto, prolateral view 10 ditto, ventral view 11 diagrammatic course of the insemination ducts 12 epigyne, ventral view 13 spermathecae; dorsal view. Scale bars - 0.1 mm (3–8, 11–12), 0.5 mm (10); 1 mm (2).
Turkey (Fig.
First author re-examined Aelurillus material from
A. cretensis
A. steliosi
A. cretensis:
Allotype of Aelurillus steliosi: 1 ♀ (MNHN #AR 13335) “GREECE, Crete, Psiloreitis, Kouroutes (Prefectura Irakleio), near Agios Titos church, 1180 m a.s.l., 35°20'N, 25°08'E, 12 June 2001, coll. S. Simaiakis”. Holotype of Aelurillus cretensis: ♂ (NHMC) GREECE, Crete, Lefka Ori Mts., 1650 m a.s.l., 35°17'N, 23°54'E, 8 June 1991, coll. P. Lymperakis. Paratypes: GREECE: 1 ♂ (NHMC), 1 ♂ (MMUM) Crete, Lefka Ori Mts., 1650-2100 m a.s.l., 35°17'N, 23°54'E, 16-17 October 1990, coll. P. Lymperakis; 7 ♂ 2 ♀ (ISEA 000.516), 1 ♀ (ISEA 000.517), 2 ♂ 2 ♀ (NHMC), 1 ♀ (MMUM) Crete, Lefka Ori Mts., 1650 m a.s.l., 35°17'N, 23°54'E, 8 June-6 October 1991, coll. P. Lymperakis; 1 ♀ (ISEA 000.711) Crete, Lefka Ori Mts., 2000 m a.s.l., 35°17'N, 23°54'E, 6 August 1992, coll. P. Lymperakis.
1 ♀ (SNHM) Greece, Crete, Lasithi, mountains S of Sitia, stony, moist beds of stream, under stones and on ground, 35°10'N, 26°06'E, 22 March 1958, coll. H. Kahmann.
Only known from Crete, Greece (Fig.
The male holotype and the female allotype of A. steliosi belong to two different species, A. cretensis (female) and A. leipoldae (male).
Aelurillus sp. 1:
A. v-insignitus:
Holotype: ♂ (IZSB) BULGARIA, Blagoevgrad Province, Strouma Valley, 2 km S of Kamenitsa, 170-240 m a.s.l., 41°38'N, 23°09'E, soil traps, 28 September – 2 February 2002, coll. M. Langourov & S. P. Lazarov. Paratypes: MACEDONIA: 1 ♂ (ISEA 000.472) Skopje, Radišani [=Radishani], 42°04'N, 21°27'E, 3 September 1995, coll. M. Komnenov. BULGARIA: 4 ♂ (IZSB) Blagoevgrad Province, Strouma Valley, FM 71, 2 km S of Kamenitsa, 170-240 m a.s.l., 41°37'N, 23°09'E, soil traps, 28 September – 2 February 2002, coll. M. Langourov & S. Lazarov. AZERBAIJAN: 1 ♂ (MMUM) 60 km SW of Baku [=Bakı], Gobustan [=Qobustan], Gobustan Rock Art Cultural Landscape, 40°05'N, 49°24'E, 7.05.1989, coll. P. M. Dunin.
Aelurillus deltshevi sp. n. belongs to A. v-insignitus-group and is closely related to A. alboclypeus sp. n., A. guecki, A. steinmetzi and A. v-insignitus; it also shares the same colour pattern on the eye field (Fig.
Aelurillus deltshevi sp. n.: 20 male, body pattern 21 left palp, ventral view 22 ditto, retrolateral view 23 palpal femur, prolateral view 24 embolic division, ventral view 25 ditto, prolateral view 26 ditto, retrolateral view 27 embolic division, ventral view 28 male face;. Scale bars - 0.1 mm (21–22, 24–27), 0.5 mm (23); 1 mm (20).
This species is named after Prof. Christo Deltshev, the well-known Bulgarian arachnologist.
Male (Paratype, from Bulgaria): Carapace 2.8 long, 2.0 wide, 1.6 high at PLE. Ocular area 1.1 long, 1.55 wide anteriorly and 1.55 wide posteriorly. Diameter of AME 0.45. Abdomen 1.3 long, 1.2 wide. Cheliceral length 1.0. Clypeal height 0.3. Length of leg segments: I 1.4+0.7+0.9+0.65+0.55; II 1.5+0.9+0.9+0.6+0.6; III 1.9+0.9+1.4+1.3+0.65; IV 1.9+0.8+1.3+1.5+0.8. Leg spination: I: Fm d 1–1–5; Pt pr and rt 1; Tb pr 1–2, v 1–1–2 ap; Mt pr and rt 1–1, v 2–2 ap. II: Fm d 1–2–5; Pt pr and rt 1; Tb pr 1–1–1, v 1–1–2 ap; Mt pr and rt 1–1, v 2–2 ap. III: Fm d 1–3–5; Pt pr and rt 1; Tb d 1–0–0, pr and rt 1–1–1–1, v 1–0–2 ap; Mt d 1–1–0, pr and rt 1–0–2, v 1–1–2 ap. IV: Fm d 1–2–5; Pt pr and rt 1; Tb d 1–0–0, pr and rt 1–1–1–1, v 1–0–2 ap; Mt d 1–1–0, pr 1–1–2, rt 1–0–2, v 1–1–2 ap. Coloration: Carapace dark brown, with black eye field, covered with adpressed white scales, more densely on its sides. Carapace with two dorsal longitudinal white stripes. Eye field covered with black shining scales, with no colour pattern (Fig.
Aelurillus deltshevi sp. n. was hitherto identified as A. v-insignitus. There are two subspecies of A. v-insignitus, A. v. morulus (Simon, 1937) from France, and A. v. obsoletus (Kulczyński in Chyzer and Kulczyński 1891) from Hungary. Simon (1937: p. 1267) commented that in southern France A. v. morulus would occur together with A. v-insignitus. This species is a local form and can be distinguished from A. v-insignitus by the abdomen and femur coloration (see p. 1227). Kulczyński (1891: p. 30) stated that A. v-insignitus and A. v. obsoletus were similar in the body colouration, but that of the eye field in A. v. obsoletus was not adequately visible (“areae huius pictura parum definita”). One of us (GA) tried to find the holotypes of both Simon’s and Kulczyński’s species but failed. It is most likely that they were lost. A. deltshevi sp. n., described here, has the black eye field, without a “V” pattern. According to Kulczyński’s picture (1891: plate 1, figs 4 a–b), the tibial apophysis is typical of A. v-insignitus. The TA in A. deltshevi sp. n. is different as the dorso-lateral branch of the TA in these species is not higher than in A. v-insignitus, and the ventro-lateral branch of the TA is less curved (Figs
Macedonia, Bulgaria and Azerbaijan (Fig.
Aelurillus deltshevi sp. n. occurs in Macedonia and Bulgaria at the elevations below 500 m a.s.l., while A. v-insignitus has been recorded from the elevations above 500 m a.s.l..
Asianellus leipoldae
Aelurillus leipoldae:
Aelurillus steliosi
Aelurillus cretensis:
Holotype of Aelurillus steliosi: ♂ (MNHN #AR 13334) “GREECE, Crete, Skalani (Pref. Irakleio), 230 m a.s.l., 35°17'N, 25°11'E, 21 May 2001, coll. S. Simaiakis”. Holotype of Asianellus leipoldae ♂ (SMNK, 2177) “GREECE, Kreta, Paleohóra, Küstengebirge” [=Crete, Palaiochora, Coastal Ranges, 35°13'N, 23°40'E], 9.01.1993 (D. Leiopold). Paratype of Asianellus leipoldae 1 ♂ (PCHM) “Kreta [=Crete], Chania, 35°18'N, 23°48'E, 4.09.1974 (A. Senglet).
GREECE: 10 ♂ 2 ♀ (ISEA 001.4045, 001.4047, 001.4058) Crete, Chania, Lefka Ori Mts., 800 and 1650 m a.s.l., 35°17'N, 23°54'E, 23 November 1990, 6 July–6 November 1991, coll. P. Lymperakis; 2 ♀ (ISEA 001.4057) Gavdos Island, Chania, Lavrakas sand-dunes, Juniperus forest, 34°52'N, 24°04'E, 24 July–8 November 1997, coll. K. Paragamian; 1 ♂ (LM) Crete, September 2002, coll. S.L. Felton; 1 ♀ (SNHM) Crete, Chania, N of Lake Curna [=Kournas], N slope, 100 m from the coast, Luminacea, Salvia, 0-15 m a.s.l., 35°20'N, 24°16'E, 16 April 1958, coll. H. Kahmann; 1 ♀ (SNHM) Crete, Heraklion, 2 km SE of Zaros, NE slope, flat hill, sandy, Phrygana, Cirsium, Cystus, under stones, 35°07'N, 24°55'E, 7 April 1958, coll. H. Kahmann.
The holotype of Aelurillus steliosi is conspecific with that of A. leipoldae. Both specimens examined (the male holotypes of A. leipoldae and A. steliosi) have the same body coloration and structure of the palpus and the embolic division (Figs
Male of Aelurillus leipoldae (holotype of Aelurillus steliosi) and female of A. cretensis (allotype of A. steliosi): 29 left palp, ventral view 30 ditto, retrolateral view 31 embolic division, dorsal view 32 diagrammatic course of the insemination ducts 33 epigyne, ventral view 34 spermathecae, dorsal view. Scale bars - 0.1 mm (29–31, 33–34).
Only known from Crete, Greece (Fig.
We wish to express our warmest thanks to all curators for the loans of specimens. T. Danişman (Kırıkkale, Turkey) is thanked for providing us material from his papers. Also many thanks to colleagues who helped us during preparation of this paper: R. Bosmans (Ghent, Belgium), K. Boğaç Kunt (Ankara, Turkey), M. Chatzaki (Alexandroupoli, Greece), V. Hula (Brno, Czech Republic), D.V. Logunov (Manchester, UK), Yu.M. Marusik (Magadan, Russia), A. Russell-Smith (Sittingbourn, UK), I. Stathi (Heraklion, Greece). D.V. Logunov and W. Wesołowska are thanked for their critical comments that helped us to improve the manuscript. This work was partly supported (GA) by the Russian Federal Fundamental Scientific Research Programme for 2013–2020 (#VI.51.1.7).
Material (the studied material was partly published by