Abstract Abstract
This study summarises all available information on the bees of the genus Sphecodes in the Arabian Peninsula and surrounding countries (Israel, Jordan, and Syria). Twenty-six species are currently known from this area, while five species are newly recorded from the Arabian Peninsula: Sphecodes atlanticus Warncke, 1992 (Saudi Arabia, Yemen), S. intermedius Blüthgen, 1923 (UAE), S. nomioidis Pesenko, 1979 (UAE, Oman), S. puncticeps Thomson, 1870 (Saudi Arabia), and S. turanicus Astafurova & Proshchalykin, 2017 (Saudi Arabia). In addition, twelve species are newly recorded from Jordan, six for Syria, and four for Israel. The female of S. atlanticus Warncke, 1992 and the male of S. dathei Schwarz, 2010 are here described for the first time and a lectotype is designated for S. intermedius Blüthgen, 1923.
Keywords: Anthophila , Apiformes , cleptoparasites, fauna, lectotype, taxonomy
Introduction
The present paper is part of a series of studies dealing with the bees of the genus Sphecodes of the territory of the Palaearctic region (Warncke 1992; Bogusch and Straka 2012; Özbek et al. 2015; Astafurova and Proshchalykin 2014, 2015a, b, c, 2016a, b, 2017a, b, c, 2018; Astafurova et al. 2014, 2015, 2018a, b, c, d). The goal of this survey is to improve the knowledge on the taxonomy and distribution of Sphecodes in the Arabian Peninsula and surrounding countries (Israel, Jordan and Syria) (Fig. 1) as an essential foundation for advanced biogeographical investigations.
Figure 1.
Map of the Arabian Peninsula and surrounding lands.
For a long time, the Arabian bee fauna has been one of the lesser sampled faunas of the world. But in recent years significant progress has been made towards a better knowledge of the bees from the Arabian Peninsula, in particular regarding the family Halictidae (Dathe 2009, Engel et al. 2013). A first contemporary inventory of the Halictidae of the Arabian Peninsula was compiled by Ebmer (2008) and Dathe (2009). Later, additional species have been described and recorded by Pesenko and Pauly (2009), Schwarz (2010), Alqarni et al. (2014), Bossert (2017), and Ascher and Pickering (2019) so that there are currently 82 species from 13 genera of family Halictidae known from this area, but the Sphecodes fauna of Arabian Peninsula is particularly under-recorded.
Probably the first information on the genus Sphecodes Latreille from the Arabian Peninsula and its adjacent lands was published by Lepeletier de Saint Fargeau (Lepeletier de Saint Fargeau and Audinet-Serville 1825), who described S. olivieri from ‘Arabie’. Almost two centuries later, in his monograph on the Western Palaearctic Sphecodes, Warncke (1992) recorded several species from Israel, Syria and Lebanon (Table 1). The list of bees of the Arabian Peninsula published by Dathe (2009) included two Sphecodes species: S. olivieri and S. longuloides Blüthgen. In the recently published third volume of the “Arthropod fauna of UAE”, Schwarz (2010) described S. dathei and S. villosulus and recorded S. marginatus Hagens and S. pinguiculus Pérez from the United Arab Emirates. In total, nineteen Sphecodes species have been recorded from the Arabian Peninsula and its adjacent lands so far (Table 1). The genus Sphecodes is not yet documented from Kuwait, Bahrain, or Iraq. Clearly this cosmopolitan genus is present in these countries and it is only a matter of time before the fauna is sampled and recorded.
Table 1.
Checklist of the Sphecodes species of the Arabian Peninsula and surrounding lands including distribution by countries.
Species | Arabian Peninsula | surrounding lands | ||||||||
---|---|---|---|---|---|---|---|---|---|---|
UAE | Oman | Qatar | Saudi Arabia | Yemen | Lebanon | Israel | Jordan | Syria | ||
1 | S. alternatus Smith | ○● | ● | ○ | ||||||
2 | S. atlanticus Warncke | ● | ● | |||||||
3 | S. barbatus Blüthgen | ● | ||||||||
4 | S. dathei Schwarz | ○● | ● | ● | ||||||
5 | S. dusmeti Blüthgen | ○ | ||||||||
6 | S. ephippius (Linnaeus) | ○ | ○ | |||||||
7 | S. gibbus (Linnaeus) | ○● | ● | |||||||
8 | S. intermedius Blüthgen | ● | ○● | ● | ||||||
9 | S. longuloides Blüthgen | ○ | ||||||||
10 | S. longulus Hagens | ● | ○● | ○● | ||||||
11 | S. majalis Pérez | ● | ||||||||
12 | S. marginatus Hagens | ○ | ● | ● | ||||||
13 | S. monilicornis (Kirby) | ○ | ○● | ● | ||||||
14 | S. nomioidis Pesenko | ● | ● | ○ | ||||||
15 | S. olivieri Lepeletier | ○● | ● | ○ | ● | ○● | ● | |||
16 | S. pellucidus Smith | ● | ● | |||||||
17 | S. pinguiculus Pérez | ○ | ● | ● | ○● | ● | ||||
18 | S. puncticeps Thomson | ● | ○● | ● | ● | |||||
19 | S. rubicundus Hagens | ● | ||||||||
20 | S. rubripes Spinola | ○ | ● | ○ | ||||||
21 | S. ruficrus (Erichson) | ○ | ● | |||||||
22 | S. rufiventris (Panzer) | ○ | ● | |||||||
23 | S. tadschicus Blüthgen | ● | ||||||||
24 | S. turanicus Astafurova & Proshchalykin | ● | ||||||||
25 | S. schenckii Hagens | ○ | ● | ● | ||||||
26 | S. villosulus Schwarz | ○● | ● | |||||||
Total: | 9 | 4 | 1 | 7 | 2 | 1 | 16 | 15 | 9 | |
12 | 20 |
White circle – published records (Meyer 1924; Warncke 1992; Dathe 2009; Schwarz 2010; Ascher and Pickering 2019); black circle – current data. Genus Sphecodes are not known in Kuwait, Bahrain, and Iraq.
Based on a comprehensive study of specimens in various collections, we here list 23 species of the genus Sphecodes, with five species recorded from the Arabian Peninsula for the first time. Additionally, twelve species are newly recorded from Jordan, six species newly recorded from Syria, and four species newly recorded from Israel. The female of S. atlanticus Warncke, 1992 and the male of S. dathei Schwarz, 2010 are here described for the first time and a lectotype is designated for S. intermedius Blüthgen, 1923.
Materials and methods
The results presented in this paper are based on 235 specimens collected in the Arabian Peninsula and surrounding territories and currently housed in the Natural History Museum (London, UK, NHMUK); the Zoological Institute, Russian Academy of Sciences(St. Petersburg, Russia, ZISP); Museum für Naturkunde der Humboldt Universität zu Berlin, Germany (ZISP), Senckenberg Deutsches Entomologisches Institut, Müncheberg, Germany (SDEI), Oberösterreichisches Landesmuseum, Biologiezentrum, Linz, Austria (OLBL) and the private collection of Maximilian Schwarz (Ansfelden, Austria, OLBL/PCMS). The following acronyms are used for the collections where type specimens are deposited:
BLCUUtah State University, Bee Biology and Systematics Laboratory, Logan, Utah, USA;
ISZPInstitute of Systematics and Evolution of Animals, Polish Academy of Sciences, Krakow, Poland;
MNHNMuséum National d’Histoire Naturelle Paris, France;
MRSNMuseo Regionale di Scienze Naturali, Torino, Italy;
MZLULund University, Lund, Sweden;
NHMUK Natural History Museum, London, UK;
ZMUKUniversity of Copenhagen, Zoological Museum, Copenhagen, Denmark;
ZSNZoologische Staatssammlung, München, Germany.
The taxonomy and distribution of species follows that of Warncke (1992), Bogusch and Straka (2012), and Astafurova and Proshchalykin (2017b). Identification keys are available in Warncke (1992), Astafurova and Proshchalykin (2017b) or Astafurova et al. (2018b), except for the two recently described new species (S. dathei and S. villosulus). A detailed synonymy can be found in Astafurova and Proshchalykin (2016b, 2017b). Morphological terminology follows that of Engel (2001) and Michener (2007). The ventral surface of some flagellomeres bear a distinctive patch of sensilla trichodea A (sensu Årgent and Svensson 1982), which we refer to as ‘tyloids’, easily observable under the microscope. Abbreviations F, T, and S are used for flagellomere, metasomal tergum and metasomal sternum respectively. The density of integumental punctures is described using the following formula: puncture diameter (in μm) / ratio of distance between punctures to average puncture diameter, e.g., 15–20 μm / 0.5–1.5. Integumental sculpture other than distinctive surface punctation is described following Harris (1979): areolate – coarse, contiguous punctures; reticulate – superficially net-like or network of raised lines; rugose – irregular, nonparallel, wrinkled raised lines (rugae); rugulose – minutely rugose; strigate – narrow, transverse or longitudinal streaks (strigae), variety of parallel lineations; tessellate – regular network of shallow grooves with flat interspaces.
Specimens were studied with a Leica M205A stereomicroscope and photographs taken with a combination of stereomicroscope (Olympus SZX10) and digital camera (Canon EOS70D). Final images are stacked composites using the program Helicon Focus 6. All images were post-processed for contrast and brightness using Adobe Photoshop.
New distributional records are noted with an asterisk (*).
Taxonomy
List of species
Sphecodes alternatus
Smith, 1853
C46A4EBF76A657D3964CC99B537BC064
Sphecodes alternatus Smith, 1853: 36, ♀ (syntypes: ♀♀, Albania; NHMUK).
Sphecodes punctiventris Hagens, 1882; S. gracilior Morawitz, 1893; S. antigae Tournier, 1901; S. reticulatus var. algeriensis Alfken, 1914; S. alternatus lindbergi Pittioni, 1950 (Synonyms).
Diagnosis.
See Astafurova et al. 2018a: 6.
Material examined.
ISRAEL: 1 ♀, Rehovot s.l., 29.IV.1975, K.M. Guichard (NHMUK 013380375); JORDAN: 1 ♀, 10 km N Petra, 3.V.1996, M. Halada (OLBL/OLBL/PCMS).
Published records.
Warncke 1992: 47, map (Israel, Syria); Ascher and Pickering 2019 (Israel).
Distribution.
Israel, *Jordan, Syria; North Africa, South and Central Europe, Russia (east to Khakassia Republic), Turkey, Caucasus, Iran, Central Asia, Kazakhstan, NW China.
Sphecodes atlanticus
Warncke, 1992
F3062642680F57EA9FB353FA0E5078C1
Figures 2–7.
Head, females, frontal view. 2Sphecodes majalis Pérez 3S. scabricollis Wesmael 4S. barbatus Blüthgen 5S. atlanticus Warncke 6S. rubripes Spinola 7S. albilabris (Fabricius). Scale bars: 1.0 mm.
Figures 8–11.
Mesosoma (8–10), dorsal view; lectotype labels (11). 8Sphecodes scabricollis Wesmael, male 9, 10S. atlanticus Warncke (9 – male, 10 – female) 11S. intermedius Blüthgen, label of lectotype. Scale bars: 1.0 mm.
Figures 16–19.
T1 (16, 17), metasoma (18, 19), females, dorsal view. 16Sphecodes majalis Pérez 17S. barbatus Blüthgen 18S. scabricollis Wesmael 19S. atlanticus Warncke. Scale bars: 1.0 mm.
Figures 22–25.
Genitalia, males, dorsal view. 22Sphecodes atlanticus Warncke 23S. scabri collis Wesmael 24S. dathei Schwarz 25S. crassus Thomson. Scale bars: 0.25 mm.
Sphecodes atlanticus Warncke, 1992: 25, Abb. 17, ♂ (holotype: ♂, Algeria: Hoggar-Geb., Guelta; OLBL/PCMS), examined.
Diagnosis.
This species is similar to the Trans-Palaearctic Sphecodes scabricollis Wesmael, 1835 owing to the flat genal area, the developed preoccipital lateral carina, the densely punctate head and mesoscutum, the size and shape of male antennal tyloids, and in the similar gonostylar shape. However, S. atlanticus differs from S. scabricollis by a number of characters outlined in Table 2. In addition to presence of preoccipital lateral carina, S. atlanticus clearly differs from the gibbus species group (S. anatolicus Warncke, 1922, S. gibbus (Linnaeus, 1758), S. nippon Meyer, 1922, S. rufiventris (Panzer, 1798), S. schenckii Hagens, 1882, S. tadschicus Blüthgen in Popov, 1935; see Astafurova et al. 2018a) by a short distance from top of head to upper margin of lateral ocellus (2 lateral ocellar diameters as seen in dorsal view, versus those with a long vertex where this distance is at most 2.5–3.0 diameters).
Table 2.
Differences between Sphecodes atlanticus Warncke, 1992 and S. scabricollis Wesmael, 1835.
Characters | Sphecodes atlanticus | Sphecodes scabricollis |
---|---|---|
Both sexes | ||
Distance from top of head to upper margin of lateral ocellus as seen in frontal and dorsal views | about one lateral ocellar diameters (Fig. 5) | about two lateral ocellar diameters (Fig. 3) |
Propodeal triangle/metaposnotum | equal (in female) or longer (in male) than mesoscutellum (Figs 9, 10) | distinctly shorter than mesoscutellum (Figs 8) |
Metasomal terga | with coarser and denser punctures (Fig. 19) | with fine and sparser punctures, especially on T1 (Fig. 18) |
Male | ||
Mesoscutum | punctures separated by at most 1.5–2.0 puncture diameters; polished between punctures (Fig. 9) | areolate (Fig. 8) |
Genitalia | gonocoxite dorsally with weak impression; gonostylar process longer (Fig. 22) | gonocoxite dorsally without impression; gonostylar process shorter (Fig. 23) |
Female | ||
Paraocular areas | with dense pubescence obscuring integument (Fig. 5) | with sparse pubescence not obscuring integument (Fig. 3) |
Description of hitherto unknown female.
Total body length 6.5–8.5 mm. Head (Fig. 5) black (except reddish mouthparts); transverse, 1.3 times as wide as long; vertex elevated, distance from top of head to upper margin of lateral ocellus ca. one lateral ocellar diameter as seen in frontal view and ca. two lateral ocellar diameters as seen in dorsal view; F1 and F2 transverse, 0.7–0.8 times as long as wide; F3 as long as wide; face with fine contiguous punctures (10–20 μm), clypeus with shiny interspaces between punctures separated by 0.1–0.5 of a puncture diameter; mandible with an inner tooth; paraocular areas and upper part of gena with dense adpressed, snow-white, plumose pubescence obscuring the integument.
Mesosoma black; mesoscutum with coarse punctures (25–50 μm) separated by at most a puncture diameter (Fig. 10); mesoscutellum with irregular punctures separated by 0.1–4 puncture diameters; mesepisternum densely reticulate-rugose; propodeal triangle coarsely reticulate-rugose with large shiny, smooth interspaces between wrinkles (Fig. 10); lateral parts of propodeum finely and densely strigate or strigate-rugose with granulate interspaces between wrinkles; vertical part of propodeum smooth with coarse and dense punctures; legs reddish or dark brown. Hind wing costal margin with 9–10 hamuli.
Metasoma (Fig. 19) with colouration varying from red on T1–T4 to entirely dark-brown; tergal discs with coarse and dense punctures (20–30 μm/ 0.5–2, sparser on anterior third of T1), marginal zone impunctate except on T1 with dense punctures (10–20 μm / 0.5–2); sterna finely tessellate with coarse setae pores; pygidial plate dull, as wide as metabasitarsus.
Material examined.
SAUDI ARABIA: 6 ♂♂, Wadi Majarish (below Taif), 12.II.1983, K. Guichard (NHMUK 013380451, 013380453, 013380460, 013380462, 013380466, 013380459); 4 ♂♂, Fayfa, 200 m, 29.I. 1983, K. Guichard (NHMUK 013380452, 013380461, 013380463, 013380464); 1 ♂, Lodar, 800 m, 16.V.1967, K. Guichard (NHMUK 0133804446); 1 ♂, Abu Arish, 26.III.1980, K. Guichard (NHMUK 013380465); 2 ♀♀, 1 ♂, Abu Arish, Jizzan Hot Springs, 25.III.1980, K. Guichard (NHMUK 013380458, 013380441, 013380454), 1 ♂, idem, 28.I.1983 (NHMUK 013380450); 1 ♀, Wadi Maraba, 25.I.1983, 1000 m, K. Guichard (NHMUK 013380457); 1 ♀, Jeddah, Locust Research Station, 17.I.1972, A. Basha (NHMUK 013380442); YEMEN: 1 ♂, Usaifira, 1 mile N Ta’izz, 4.500 ft, 21.XII.1937, H. Scott, E. Britton (NHMUK 013380468), 1 ♂, Wadi Maytam, 12 km SE Ibb, 1600 m, 13°53'N, 44°18'E, 27.X.2005, J. Halada (OLBL/PCMS); 2 ♀♀, 3 ♂♂, Hawf NE Albhaydah, 200–730 m, 16°53'N, 53°05'E, 14.X.2005, J. Halada (OLBL/PCMS); 2 ♀♀, 4 ♂♂, 20 km S Taizz, 1200 m, 13°30'N, 43°57'E, 24.X.2005, J. Halada (OLBL/PCMS); 2 ♂♂, Jabal Bura, NEE Al Hudaydah, 200–800 m, 14°52'N, 43°24'E, 30.X-1.XI.2005, J. Halada (OLBL/PCMS); 1 ♂, Wadi Aniz, SSW Sana, 1520 m, 14°60'N, 44°09'E, 7.X.2005, J. Halada (OLBL/PCMS).
Distribution.
*Saudi Arabia, *Yemen; Algeria, the Canary Islands.
Sphecodes barbatus
Blüthgen, 1923
517471C21052533F97CAE88F4771CD29
Sphecodes barbatus Blüthgen, 1923: 497–498, ♀ (holotype: ♀, Turkey, Ak-Chehir; ZSM).
Diagnosis.
Sphecodes barbatus is very similar to S. majalis. The two species are easily separable in the female, but males are difficult. The female S. barbatus differs from S. majalis by denser, distinctly plumose pubescence on paraocular areas and clypeus (Fig. 4) (sparser, weakly plumose or simple pubescence in S. majalis, Fig. 2) and by a distinctly (Fig. 17) punctate T1 (sparse and tiny punctures in S. majalis, Fig. 16).
Material examined.
SYRIA: 1 ♀, Syria, 40 km NE Damaskus, 22.V.1996, H. Halada (ZISP); 2 ♂♂, Slenfe, 1200 m, 19.IV.1986, K.M. Guichard, (NHMUK 013380371, 013380372).
Distribution.
*Syria; Greece, Turkey.
Remarks.
Warncke (1992) interpreted Sphecodes barbatus as a subspecies of S. majalis Pérez, 1903, but later this taxon was restored as a valid species (Bogusch and Straka 2014a).
Sphecodes dathei
Schwarz, 2010
6D4AD2DBEB885FA39206B98C83009AB9
Figures 12–15.
Sphecodes dathei Schwarz, male. 12 Head, frontal view 13 antenna, frontal view 14 mesosoma, dorsal view 15 T1, dorsal view. Scale bars: 1.0 mm.
Sphecodes dathei Schwarz, 2010: 483–486, ♀, plates 1–12 (holotype: ♀, United Arab Emirates, Wadi Shawkah, 25°06'N, 56°02'E, 9–24.VI.2007, in water trap, A. van Harten leg.; SDEI), examined.
Diagnosis.
The species is similar to Sphecodes crassus Thomson, 1870 owing to the wide female metafemur (strongly enlarged in the basal half); strongly transverse female head; sparsely punctate mesoscutum in both sexes, weakly developed male antennal tyloids (usually covering less than 1/3 of ventral flagellar surfaces). The female of Sphecodes dathei differs from S. crassus by dense, apressed, snow-white, plumose pubescence obscuring integument in paraocular areas (sparse, simple pubescence not obscuring integument in S. crassus); the male differs by densely and relatively coarsely punctate T1 (in S. crassus T1 usually with a few fine punctures, rarely with relatively coarse and dense punctures). Both species have similar gonostylar shape, but S. dathei has a narrower, trapezoidal membranous portion of the gonostylus (wider, close to oval in S. crassus, Fig. 25).
Description of hitherto unknown male.
Total body length 5.0–6.5 mm. Head (Fig. 12) black (except reddish mouthparts and brownish antenna); weakly transverse, 1.1 times as wide as long; vertex not elevated; distance from top of head to upper margin of lateral ocellus ca. two lateral ocellar diameters as seen in dorsal view; antenna (Fig. 13) reaches posterior margin of mesoscutum; F1 transverse, 0.6 times as long as wide; F2 long, 1.7 times as long as wide; remaining flagellomeres 1.2–1.3 times as long as wide; tyloids weakly developed (on F2–F4 covering less than 1/6 of ventral flagellar surfaces and from F5 onward covering less than 1/3); clypeus, frons, supraclypeal and paraocular areas with fine contiguous punctures (10–20 μm); ocello-ocular area and gena with shiny interspaces, punctures separated by 0.5–1 a puncture diameter; face below and above the antennal toruli with dense adpressed snow-white plumose pubescence obscuring integument; gena with similar pubescence, but not obscuring integument.
Mesosoma (Fig. 14) black; mesoscutum and mesoscutellum with punctures (20–25 μm) separated by 0.5–4 puncture diameters; mesepisternum and hypoepimeral area densely reticulate-rugose; propodeal triangle (Fig. 14) and vertical part of propodeum coarsely reticulate-rugose with shiny, smooth interspaces between wrinkles; lateral parts of propodeum coarse reticulate- to strigate-rugose with shiny interspaces between wrinkles; legs dark brown, but tarsi and partially tibia yellow or reddish. Hind wing costal margin with 5 hamuli.
Metasomal T1–T3 red (T1 black basally, T3 – apically); tergal discs (Fig. 15) with dense punctures (10–15 μm / 0.5–1), becoming sparse along marginal zone on T1; marginal zones smooth, impunctate; sterna with numerous microscopic setae pores; gonocoxite dorsally with a deep impression; membranous portion of gonostylus small, trapezoidal (Fig. 24).
Material examined.
SAUDI ARABIA: 1 ♀, Wadi Majarish, 800 m, 12.II.1983, K. Guichard (NHMUK 013380455); UNITED ARAB EMIRATES: 1 ♀, Hatta, 24.IV.1992 (NHMUK 013380414); 1 ♂, idem, 19–20.V.1988 (NHMUK 013380431); 7 ♂♂, idem, 14.IV.1990, I. Hammer (NHMUK 013380428, 013380429, 013380430, 013380432, 013380433, 013380434, 013380430); YEMEN: 1 ♀, Lawdar, NE Aden, 1140 m, 13°53'N, 45°48'E, 28.X.2005, J. Halada (OLBL/PCMS).
Published records.
Schwarz 2010: 483 (United Arab Emirates).
Distribution.
United Arab Emirates, *Saudi Arabia, *Yemen.
Sphecodes gibbus
(Linnaeus, 1758)
5F913968CCE556978526570A1C4BB74D
Sphex gibba Linnaeus, 1758: 571, ♀ (syntypes: ♀♀, Sweden; ZMUK).
Apis glabra Füessly, 1775; Andrena ferruginea Olivier, 1789; Apis gibbosa Christ, 1791; Melitta sphecoides Kirby, 1802; M. picea Kirby, 1802; Andrena austriacaFabricius, 1804; Dichora analis Illiger, 1806; Sphecodes apicatus Smith, 1853; S. nigripennis Morawitz, 1876; S. sutor Nurse, 1903; S. gibbus var. rufispinosus Meyer, 1920; S. g. var. turkestanicus Meyer, 1920; S. castilianus Blüthgen, 1924; S. pergibbus Blüthgen, 1938; S. lustrans Cockerell, 1931; S. angarensis Cockerell, 1937 (Synonyms).
Diagnosis.
See Astafurova et al. 2018a: 17.
Material examined.
JORDAN: 1 ♀, Jordan Valey, Dayr Alla, 27.IV.1996, M. Halada (OLBL/PCMS); 1 ♀, N. Shuna env., 20–22.IV.1996; 1 ♀, idem, 29–30.IV.1996, M. Halada (OLBL/PCMS); SYRIA: 1 ♂, 20 km NE Latakia, 25.V.1996, M. Halada (OLBL/PCMS); ISRAEL: 1 ♀, Rehovot s.l., 29.IV.1975, K.M. Guichard (NHMUK 1975-248, 013380378); 1 ♀, Ein Gedi, 200 m, 11.III.1975, K.M. Guichard (NHMUK 1975-154, 013380379); 1 ♂, Jericho (Wadi Quilt), 250 m, 13–22.V.1975, K.M. Guichard (NHMUK 1975-248, 013380373); 1 ♀, Jericho, 200 m, 6–27.III.1975, K.M. Guichard (NHMUK 1975-154, 013380374).
Published records.
Warncke 1992: 30 (Israel).
Distribution.
Israel, *Jordan; North Africa, Europe (north to 63°), Russia (east to Yakutia), Turkey, Iran, Pakistan, Central Asia, Kazakhstan, Mongolia, NW China, India.
Sphecodes intermedius
Blüthgen, 1923
7CC2FBA91AFE532A829B9A3365B2C600
Sphecodes intermedius Blüthgen, 1923: 500 (lectotype (designated here): ♂, Type <red label> // Caucas Portz // Sph. intermedius ♂, Type., P. Blüthgen det. // <blue circle> // Lectotypus, Sphecodes intermedius Blüthgen, 1923, ♂, des. Astafurova & Proshchalykin, 2018; paralectotype: ♀, Type <red label> Sph. intermedius ♀, Type, P. Blüthgen det. // Paralectotypus, Sphecodes intermedius Blüthgen, 1923, ♀, des. Astafurova & Proshchalykin, 2018; ISZP, examined, Fig. 11).
Sphecodes lactipennis Meyer, 1925 (Synonym).
Diagnosis.
See Astafurova et al. 2018a: 20.
Material examined.
UNITED ARAB EMIRATES: 1 ♂, Hatta (Hotel), 28. IV.1989, (NHMUK 013380370); 1 ♂, idem, 23.VIII.1991 (NHMUK 013380409); 1 ♂, idem, 14.IV.1990, I. L. Hamer [D. Baker det., 1992 as S. punctatissimus Meyer] (NHMUK 013380361); ISRAEL: 1 ♀, Jerusalim, 16.VII.1930, S. Bodenheimer [det. Blüthgen] (MNHB); 1 ♀, Tiberias, 200 m, 22.III.1975, K.M. Guichard (NHMUK 013380410); 1 ♀, Jericho (Hisham Palace), 200 m, 8.III.1975, K.M. Guichard (NHMUK 1975-248, 013380408); JORDAN: 1 ♀, N. Shuna env., 20–22.IV.1996; 1 ♀, idem, 29–30.IV.1996, M. Halada (OÖLM)
Published records.
Ascher and Pickering 2019 (Israel)
Distribution.
*United Arab Emirates, Israel, *Jordan; North Africa, South Europe (east to Ukraine), Russia (south of the European part, Urals), Caucasus, Turkey, Kazakhstan, Central Asia, Pakistan, China (Gansu).
Remarks.
Sphecodes intermedius Blüthgen, 1923 was described from specimens of both sexes collected in “Caucas” [Caucasus] (Fig. 11). There are two specimens (female and male) in ISZP from this locality, which correspond to the original description of P. Blüthgen. One of these specimens (male) is designated here as a lectotype of S. intermedius to avoid any confusion about the status of the type specimens and to properly diagnose this species.
Sphecodes longulus
Hagens, 1882
43EBA5F314925AF7A2E67FBE8AB2EAED
Sphecodes longulus Hagens, 1882: 226, Fig. 25, ♂ (syntypes: ♂♂, Germany; ? Dominican monastery, Venlo, Nederland).
Sphecodes longulus var. eupidus Hagens, 1882; S. nitidulus Hagens, 1882; S. subfasciatus Blüthgen, 1934; S. amakusensis Yasumatsu & Hirashima, 1951; S. sabulosus Tsuneki, 1983; S. crassicornis Tsuneki, 1983; S. tsunekii Haneda, 1994 (Synonyms).
Diagnosis.
See Astafurova et al. 2018a: 21.
Material examined.
JORDAN: 1 ♀, 30 km N Tafila, 2.V.1996, M. Halada (OLBL/PCMS); 1 ♂, 20 km SW Madaba, 26.V.2007, 400 m, Z. Kejval (OLBL/PCMS); 1 ♂, Ajlun, 35 km W Jarash, 850 m, Z. Kejval (OLBL/PCMS); 1 ♀, 20 km S North Shuna Tall al Arbatin, 19.IV.1996, M. Halada (OLBL/PCMS); ISRAEL: 1 ♂, Dafna, 27.V.1991, K. Warncke (OLBL/PCMS); 1 ♂, North Galeleya, Nature Reserve ”Khule”, 23.V.1968, V. Trjapitzin (ZISP); 1 ♀, 5 km W Jericho, Wadi Qelet, St. Georg Mon., 6.V.1996, O. Niehuis (OLBL/PCMS); SYRIA: 1 ♂, Damask, 20–21.V.1980, M. Halada (OLBL/PCMS).
Published records.
Warncke 1992: 17 (Syria); Ascher and Pickering 2019 (Jordan).
Distribution.
*Israel, Jordan, Syria; Europe (north to Finland, Sweden, Denmark, England), Russia (east to Far East), Turkey, Iran, Central Asia, Kazakhstan, China, Japan.
Sphecodes majalis
Pérez, 1903
8A5ED1678AF25BA98265B2151EB7EBBC
Sphecodes majalis Pérez, 1903: 219, ♀, ♂, (syntypes: ♀, ♂, France, Spain; MNHN).
Sphecodes gracilior Pérez, 1903; S. opacifrons Pérez, 1903; S. problematicus Schulz, 1906 (Synonyms).
Diagnosis.
Refer to the diagnosis S. barbarus, above.
Material examined.
JORDAN: 35 ♀ ♀, 5 ♂♂, 10 km N Petra, 3.V.1996, M. Halada (OLBL/PCMS); 2 ♀, 10 km N Jarash, 20.IV.2002, M. Snizek (OLBL/PCMS); 1 ♀, Ajlun S of Anjara, 27.IV.2002, M. Snizek (OLBL/PCMS).
Distribution.
*Jordan; North Africa, South Europe, Russia (south of the European part), Turkey, Iran.
Sphecodes marginatus
Hagens, 1882
DCA18E56EF965AF78B75623ACCAAF279
Sphecodes marginatus Hagens, 1882: 223, Fig. 18, ♂ (syntypes: 2 ♂, Germany: Cleve; ? Dominican monastery, Venlo, Nederland).
Sphecodes atratus Hagens, 1882; S. nigritulus Hagens, 1882; S. biskrensis Pérez, 1903 (Synonyms).
Diagnosis.
This species belongs to the miniatus species group (S. creticus Warncke, 1992, S. haladai Warncke, 1992, S. larochei Warncke, 1992, S. marginatus Hagens, 1882, S. miniatus Hagens, 1882, S. nomioidis Pesenko, 1979, S. schawrzi Astafurova & Proshchalykin, 2014, and S. sandykachis Astafurova & Proshchalykin, 2018), with the same length and transverse F1–F3 in females. Among species of this group S. marginatus is most close to S. miniatus and S. nomioidis as they have a similar sculpture and structure of the body. Hence females of the three species are challenging to distinguish, but the male differs from the other two species by smaller triangular gonostylus. Differences between these three species are outlined by Bogusch and Straka (2012) and between females of this species group by Astafurova et al. (2018c).
Material examined.
ISRAEL: 1 ♀, 1 ♂, Jerusalim, 18.VI.1930; 1 ♂, idem, 10.VI.1931, S. Bodenheimer [det. Blüthgen] (MNHB); JORDAN: 1 ♀, W Jordan Valey, Mubalath, 27.IV.1996, M.Halada (OLBL/PCMS); 1 ♀, n. Shuna, 20–22.IV.1996, M. Halada(OLBL/PCMS); 2 ♂♂, NW of Ailun, 850 m, 20.V.2007, Z. Kejval (ZISP); 1 ♀, Jericho (Wadi Quilt), 250 m, 6.III.1975, K.M. Guichard (NHMUK 1975-154, 013380467).
Published records.
Schwarz 2010: 486 (United Arab Emirates); Ascher and Pickering 2019 (United Arab Emirates).
Distribution.
United Arab Emirates, *Israel, *Jordan; North Africa, Europe (north to Germany and Denmark, east to Belarus).
Sphecodes monilicornis
(Kirby, 1802)
4AC06390842B516CAC0E5EECE61A4859
Melitta monilicornis Kirby, 1802: 47, ♂ (syntypes: ♂♂, England, NHMUK).
Sphecodes maculatus Lepeletier de Saint Fargeau, 1841; S. subquadratus Smith, 1845; S. ruficrus Dalla Torre, 1896; S. hanuman Nurse, 1903; S. monilicornis var. nigerrima Blüthgen, 1927; S. caucasicus Meyer, 1920; S. cephalotes Meyer, 1920; S. smyrnensis Meyer, 1920; S. monilicornis quadratus Meyer, 1920; S. monilicornis berberus Warncke, 1992; S. quadratus cephalotiformis Pittoni, 1950 (Synonyms).
Diagnosis.
See Astafurova et al. 2018a: 24.
Material examined.
SYRIA: 1 ♀, 50 km W Homs, 12.V.1996, M. Halada (OLBL/PCMS); 1 ♀, 60 km S Damask, Khabab, 14.V.1996, M. Halada (OLBL/PCMS); 1 ♀, 20 km S North Shuna Tall al Arbatin, 19.IV.1996, M. Halada (OLBL/PCMS); 1 ♀, 10 km W Jarasch, 1.V.1996, M. Halada (OLBL/PCMS); 2 ♀♀, Jisr ash Shunhur, 26.V.1996, M. Halada (OLBL/PCMS); 4 ♂♂, 20 km NE Latakia, 25.V.1996, M. Halada (OLBL/PCMS); 1 ♂, 30 km W Damask, 19.VI.2000, M. Halada (OLBL/PCMS); JORDAN: 1 ♀, Jarash env., 1.V.1996, M. Halada (OLBL/PCMS); 1 ♀, 10 km N Jarash, 1.V.1996, M. Halada (OLBL/PCMS); 1 ♂, 16 km WN Aijun, 600 m, 21.V.2077, Z. Kejval (OLBL/PCMS); 1 ♀, 10 km N Petra, 3.V.1996, M. Halada (OLBL/PCMS).
Published records.
Ascher and Pickering 2019 (Jordan).
Distribution.
Jordan, *Syria; North Africa, Europe (north to 64°), Russia (east to Far East), Caucasus, Turkey, Iran, Pakistan, Central Asia, Kazakhstan, Mongolia, China.
Sphecodes nomioidis
Pesenko, 1979
5BE05D899B75554B805681C443A35A68
Sphecodes nomioidis Pesenko, 1979: 860, ♀ (holotype: ♀, Ukraine: Donetsk Province, Yenaktsevo, 10.VIII.1978, V. Radchenko leg.; ZISP).
Diagnosis.
Refer to diagnosis for S. marginatus, above.
Material examined.
UNITED ARAB EMIRATES: 4 ♂♂, Hatta, 14.IV.1990, I. Hamer (NHMUK 013380411, 013380415, 013380416, 013380417); OMAN: 1 ♂, Rostaq, 350 m, 21–31.III.1976, K. Guichard (NHMUK 013380443).
Published records.
Bogusch and Straka 2012: 14 (Jordan).
Distribution.
*United Arab Emirates, *Oman, Jordan; South and Central Europe (west to Austria), Ukraine, Russia (SW of the European part), Turkey.
Sphecodes olivieri
Lepeletier de Saint Fargeau, 1825
8379E7A2BCD151EE998204A763B18992
Sphecodes olivieri Lepeletier de Saint Fargeau in Lepeletier de Saint Fargeau and Audinet-Serville, 1825: 448, ♂ (syntypes: ♂♂, ‘Arabie’).
Sphecodes collaris Spinola, 1843; S. hispanicus var. abyssinicus Sichel, 1865; S. ruficornis Sichel, 1865; S. punctulatus Sichel, 1865; S. subpunctulatus Sichel, 1865; S. rufithorax Morawitz, 1876; S. verticalis Hagens, 1882; S. desertus Nurse, 1903; S. chionospilus Cockerell, 1911; S. chionospilus var. sanguinatus Cockerell, 1911; S. tenuis Meyer, 1920; S. olivieri var. niveatus Meyer, 1925 (Synonyms).
Diagnosis.
See Astafurova et al. 2018a: 25.
Material examined.
UNITED ARAB EMIRATES, 1 ♂, Digdaga, 8.VIII.1984, J.N. Brown [D. Baker det, 92] (NHMUK 013380368); 1 ♂, Hatta (Hotel), 21.VIII.1987, I.L. Hamer [D. Baker det, 92] (NHMUK 013380366); 1 ♂, Soweihan Rd, 12.IV.1988, I.L. Hamer [D. Baker det, 92] (NHMUK 013380367); 1 ♂, Jebal Ali, 15.II.1991, I.L. Hamer [D. Baker det, 92] (NHMUK 013380361); SAUDI ARABIA, 1 ♀, 1♂, Jeddah, 15.II.1972, K.M. Guichard (NHMUK 013380399, 013380398); 1 ♀, 3 ♂♂, Riyadh area, 16–21.IV.1980, K.M. Guichard (NHMUK 013380456, 013380395, 013380396, 013380397); 1 ♂, Jeddah, 13.IV.1980 (NHMUK 013380393); 2 ♀♀, idem, 15.IV.1980, K.M. Guichard (NHMUK 013380392, 013380394); JORDAN: 1 ♀, 20 km W At Tafila, 1.VI.2007, Z. Kejval (OLBL/PCMS); OMAN, 1 ♀, Wadi Qurvat, Ag. Stn. 500 m, 5.III.1976, K. Guichard (NHMUK 013380383); 2 ♀♀, Tinaf, 650 m, 7.III.1976, K. Guichard (NHMUK 013380381, 013380380); 1 ♀, Rostaq, 350 m, 21–31.III.1976, K. Guichard (NHMUK 013380382);
ISRAEL, 1 ♂, Ein Bokek Zohar, 350 m, 25.V.1975, K.M. Guichard (NHMUK 1975-248, 013380385); ISRAEL: 1 ♀, Jericho (Wadi Kelt), 200 m, 6.III.1975, K.M. Guichard (NHMUK 1975-248, 013380387).
Published records.
Lepeletier de Saint Fargeau 1825: 448 (‘Arabie’); Warncke 1992: 46, map (Israel); Dathe 2009: 385 (United Arab Emirates); Schwarz 2010: 486 (United Arab Emirates); Ascher and Pickering 2019 (United Arab Emirates, Qatar).
Distribution.
United Arab Emirates, *Oman, Qatar, *Saudi Arabia, Israel, *Jordan; North Africa, South Europe, Russia (South of European part), Turkey, Caucasus, Iran, Pakistan, Central Asia, Kazakhstan, NW China.
Sphecodes pellucidus
Smith, 1845
80F345845F915F009BB3FD1A6E8B1BBD
Sphecodes pellucidus Smith, 1845: 1014, ♀, ♂ (syntypes: ♀♀, ♂♂, England; NHMUK).
Sphecodes pilifrons Thomson, 1870; S. brevicornis Hagens, 1874; S. volatilis Smith, 1879; S. pellucidus var. algirus Alfken, 1914; S. pellucidus var. hybridus Blüthgen, 1924; S. pellucidus var. niveipennis Meyer, 1925 (Synonyms).
Diagnosis.
See Astafurova et al. 2018a: 27.
Material examined.
SYRIA: 1 ♀, 30 km N Dara, Nawa, 18.V.1996, M. Halada (OLBL/PCMS); JORDAN: 1 ♀, Jordan valley, S. Shuna, 17.IV.1996, M. Halada (OLBL/PCMS); 1 ♀, 10 km N Petra, 3.V.1996, M. Halada (OLBL/PCMS).
Distribution.
*Jordan, *Syria; North Africa, Europe (north to 66°), Russia (east to Far East), Turkey, Iran, Central Asia, Kazakhstan, Mongolia, China.
Sphecodes pinguiculus
Pérez, 1903
1BA02AED9E255C609B3F70042BC8AE7F
Sphecodes pinguiculus Pérez, 1903: CCXX, ♀ (syntypes: ♀♀, Spain: Catalonia; MNHN).
Sphecodes sareptensis Meyer, 1922; S. excellens Meyer, 1922; S. punctatissimus Meyer, 1922; S. hungaricus Blüthgen, 1923; S. coelebs Blüthgen, 1923; S. consobrinus Blüthgen, 1923; S. persicus Blüthgen, 1924; S. capverdensis Pauly & La Roche, 2002 (Synonyms).
Diagnosis.
See Astafurova et al. 2018a: 30.
Material examined.
SYRIA: 1 ♂, 80 km E Palmira, 450 m, 22.IV.1992, K. Warncke (OÖLM); SAUDI ARABIA, 1 ♀, Hofut, 145 m, 21–6.IV.1980, K. Guichard (NHMUK 013380359); 1 ♀, Hatta, 10.IV.1983, I.L. Hamer (NHMUK 013380389); 1 ♀, idem, 6.VI.1986, I.L. Hamer (NHMUK 013380390); 2 ♀♀, Khor-Fakkan, 20.III.1987, I.L. Hamer (NHMUK 013380364, 013380377); 1 ♀, Soweihan Rd, 12.IV.1988, I.L. Hamer (NHMUK 013380391); OMAN, 1 ♀, Wadi Qurvat, Ag. Stn. 500 m, 5.III.1976, K. Guichard (NHMUK 013380407); 2 ♀♀, Rostaq, 350 m, 21–31.III.1976, K. Guichard (NHMUK 013380405, 013380406);
ISRAEL: 1 ♂, Tel-Aviv, 22.IV.1966, Bytinski-Salz (OLBL/PCMS); 3 ♀♀, Jericho (Hisham Palace), 200 m, 8.III.1975, K.M. Guichard (NHMUK 1975-248, 013380408).
Published records.
Schwarz 2010: 486 (United Arab Emirates, Israel); Ascher and Pickering 2019 (Israel, United Arab Emirates).
Distribution.
United Arab Emirates, *Oman, *Saudi Arabia, Israel, *Syria; Cape Verde Islands, North Africa, South Europe, Russia (east to Buryatia), Turkey, Iran, Central Asia, Kazakhstan, Mongolia, North China.
Sphecodes puncticeps
Thomson, 1870
E61D565668005FD398FBE21910268C45
Sphecodes puncticeps Thomson, 1870: 99, ♀, ♂ (syntypes: ♀♀, ♂♂, Sweden; MZLU).
Sphecodes bituberculatus Pérez, 1903; S. opacifrons Pérez, 1903; S. puncticeps var. cretanus Strand, 1921 (Synonyms).
Diagnosis.
See Astafurova et al. 2018a: 31.
Material examined.
SAUDI ARABIA: 1 ♂, Riyadh area, 16–21.IV.1980, K.M. Guichard (NHMUK 013380403); JORDAN: 1 ♀, Jordan valley, S. Shuna, 17.IV.1996, M. Halada (OLBL/PCMS); 2 ♀, 3 ♂♂, Jordan valley, Dayr Alla, 27.IV.1996, M. Halada (OLBL/PCMS); 1 ♀, 10 km N Petra, 3.V.1996, M. Halada (OLBL/PCMS); 1 ♀, 10 km SE Suwayda Kafr, 19.V.1996, M. Halada (OLBL/PCMS); SYRIA: 1 ♀, Latakia s.l., 17.VI.1986, K. Guichard (NHMUK 013380360); 2 ♀♀, 10 km SE Suwayda Kafr, 19.V.1996, M. Halada (OLBL/PCMS); ISRAEL: 2 ♂♂, Jerusalem, 21.IX.1922, P.A. Buxton (NHMUK 013380401, 013380400); 1 ♂, Rehovot s.l., 29.IV.1975, K.M. Guichard (NHMUK 1975-248, 013380404); 3 ♂♂, Jericho (Wadi Quilt), 250 m, 13–22.V.1975, K.M. Guichard (NHMUK 1975-248, 013380365, 013380376, 013380402).
Published records.
Warncke 1992: 19 (Israel); Ascher and Pickering 2019 (Israel).
Distribution.
*Saudi Arabia, Israel, *Jordan, *Syria; North Africa, Europe (north to Finland and Sweden), Russia (east to Far East), Turkey, Iran, Central Asia, Kazakhstan, Mongolia.
Sphecodes rubicundus
Hagens, 1875
68AD66DC2D4A583CBEFB7835049C7E1E
Sphecodes rubicundus Hagens, 1875: 318 (syntypes: ♂♂, ♀♀, Germany; ? Dominican monastery, Venlo, Nederland).
Sphecodes rubicundus altisilesiacus Torka, 1927 (Synonyms).
Diagnosis.
The female of this species as well as S. ruficrus is most close to S. pellucidus and S. ephippius owing to a densely punctate head and mesosoma, relative wide pygidial plate and impunctate T1, but differs by having a distinctly elevated vertex with the distance between vertex and upper margin of lateral ocellus at least a lateral ocellar diameter as seen in frontal view (versus 0.2–0.5). S. rubicundus differs from S. ruficrus by white pubescence of head and mesosoma (with brown setae in S. ruficrus) and a less curved basal (M) vein in hind wing. The male most closely resembles S. pesenkoi Astafurova & Proshchalykin, 2018 and S. ruficrus (Erichson, 1835) owing to a similar gonostylar shape (elongate, spoon-shaped). The male of S. rubicundus differs from S. pesenkoi by an areolate mesoscutum (versus punctures separated by 1–3 puncture diameters) and coarsely and densely punctate T1 (a few fine punctures in S. pesenkoi).
According to the phylogenetic analysis (Habermannová et al. 2013) Sphecodes rubicundus, S. ruficrus, S. pellucidus, and S. ephippius belong to the same clade. Relationship between these species also is well supported by morphological characters.
Material examined.
ISRAEL, 2 ♂♂, Jerusalem, 800 m, 20.III.1975, K.M. Guichard (NHMUK 1975-154, 013380388, 013380386); 1 ♀, Tiberias, 200 m, 22.III.1975, K.M. Guichard (NHMUK 1975-154, 013380384); 1 ♀, Jerusalem, 20.III.1993, D. Ahal (OLBL/PCMS).
Distribution.
*Israel; Europe (north to 56°), Russia (south of the European part), Turkey, Caucasus, Iran.
Sphecodes rubripes
Spinola, 1839
AED78E1E647A59999CE12B44195BAF69
Figures 20, 21.
Habitus, females, lateral view. 20Sphecodes albilabris (Fabricius) 21S. rubripes Spinola. Scale bars: 1.0 mm.
Sphecodes rubripes Spinola, 1839: 512, ♀ (syntypes: ♀♀, Cyprus; MRSN).
Sphecodes africanus Lepeletier, 1841; S. rufipennis Cockerell, 1931, S. atrescens Cockerell, 1931 (Synonyms).
Diagnosis.
The female of S. rubripes differs from S. albilabris by the pubescence of paraocular area (Fig. 6) with brown erect setae not obscuring integument (versus white plumose appressed pubescence obscuring integument usually with admixture of brownish erect setae in S. albilabris, Fig. 7). Both sexes also differ by mainly red legs, except brown coxae and trochanters, Fig. 21 (at most reddish tarsi and tibia in S. albilabris, Fig. 20). These two species also differ in phenology (males of S. rubripes were recorded in the early spring while males of S. albilabris were found in the summer) and have different hosts (Bogusch and Straka 2012, Cross 2017). S. albilabris is widespread in the Palaearctic from the Atlantic Ocean to Russian Far East; however, the distribution of the species in the Mediterranean Region is unclear due to confusion with S. rubripes. The past records of S. albilabris from Israel and Syria refer to S. rubripes. We examined material of S. albilabris from Morocco and Tunisia, but we do not have any specimens of S. albilabris from the Arabian Peninsula or surrounding lands.
Material examined.
JORDAN: 1 ♀, 10 km N Petra, 3.V.1996, M. Halada (OLBL/PCMS).
Published records.
Meyer 1924: 3 (Syria, as S. fuscipennis rubripes); Warncke 1992: 31 (Israel, as S. albilabris rubripes); Ascher and Pickering 2019 (Israel, as S. albilabris (Fabricius)).
Distribution.
*Jordan, Israel, Syria; North Africa, South-Western Europe, Cyprus.
Remarks.
Mayer (1924) and later Warncke (1992) interpreted Sphecodes rubripes as a subspecies of S. albilabris (Fabricius, 1793), but this taxon was restored as a valid species (Bogusch and Straka 2014b).
Sphecodes ruficrus
(Erichson, 1835)
4DD92252598B52318ED7B28E7E56E63D
Dichroa ruficrus Erichson, 1835: 101, ♀, (syntypes: ♀♀, Spain; ZMHB).
Sphecodes hispanicus Wesmael, 1836; S. rufipes Smith, 1853; S. gibbus var. tunetanus Gribodo, 1894; S. atrohirtus Pérez, 1903 (Synonyms).
Diagnosis.
Refer to diagnosis for S. rubicundus, above.
Material examined.
JORDAN: 1 ♀, W Jordan Valley, env. of S. Shuna, 17.IV.1996, M. Halada (OLBL/PCMS).
Published records.
Warncke 1992: 21 (Israel); Ascher and Pickering 2019 (Israel).
Distribution.
Israel, *Jordan; North Africa, southwestern Europe.
Remarks.
Russia is mistakenly listed as within the distribution by Bogusch and Straka (2012) as well as Turkey and Armenia by Özbek et al. (2015) due to confusion with S. ruficrus rubicundus sensu Warncke (1992).
Sphecodes rufiventris
(Panzer, 1798)
EA4EA9F64BA55BF3A1FC3AF064E687E7
Tiphia rufiventris Panzer, 1798: 4, ♀ (syntypes: ♀♀, Germany; ZMHB).
Sphecodes subovalis Schenck, 1853; S. brevis Hagens, 1875; S. singularis Meyer, 1920; S. combinatus Blüthgen, 1927; S. subovalis austrinus Erlandsson, 1979; S. rufiventris hethiticus Warncke, 1992 (Synonyms).
Diagnosis.
See Astafurova et al. 2018a: 34.
Material examined.
JORDAN: 1 ♂, W Jordan Valey, Mubalath, 27.IV.1996, M. Halada (OLBL/PCMS).
Published records.
Ascher and Pickering 2019 (Israel).
Distribution.
Israel, *Jordan; North Africa, Europe, (north to 57°), Russia (east to Khakassia Republic), Turkey, Iran, Central Asia, Kazakhstan.
Sphecodes schenckii
Hagens, 1882
30EA22E5954652D3BF5B8627DB0398EC
Sphecodes schenckii Hagens, 1882: 217, ♂ (holotype: ♂, no locality, Rudow leg. [see Blüthgen 1923: 444]; MNHB).
Sphecodes sulcicollis Pérez, 1903; S. caspicus Meyer, 1920 (Synonyms).
Diagnosis.
See Astafurova and Proshchalykin 2017b: 274.
Material examined.
JORDAN: 1 ♂, NW Ajlun, 850 m, 20.V.2007, Z. Kejval (OLBL/PCMS) ; 1 ♀, 10 km N Petra, 3.V.1996, M. Halada (OLBL/PCMS); SYRIA: 3 ♂♂, 20 km NE Latakia, 25.V.1996, M. Halada (OLBL/PCMS).
Published records.
Warncke 1992: 27 (Israel, as Sphecodes schenckii caspicus Meyer); Ascher and Pickering 2019 (Israel).
Distribution.
Israel, *Jordan, *Syria; Europe (north to Germany), Russia (European part), Turkey, Caucasus, ? Iran.
Sphecodes tadschicus
Blüthgen, 1935
C6671BF631855F19A9D51ED3E1E89547
Sphecodes tadschicus Blüthgen in Popov, 1935: 366, ♂, ♀ (holotype: ♂, near Kulab [Tajikistan], 25.VII.1935, V. Popov leg.; ZISP).
Diagnosis.
See Astafurova et al. 2018a: 39.
Material examined.
ISRAEL: 1 ♀, 8 ♂♂, Jerusalem, 10–25.VIII.1960, Bytinski (MNHB).
Distribution.
*Israel; Turkey, Iran, Central Asia, Kazakhstan.
Sphecodes turanicus
Astafurova & Proshchalykin, 2017
7D2BE7510D0857F28E38D5D19D9C4E52
Sphecodes turanicus Astafurova & Proshchalykin, 2017b: 274, ♂, ♀ (holotype: ♀, Turkmenistan, Chardzhou, 16.IV.1988, Dialentov leg.; ZISP).
Diagnosis.
See Astafurova et al. 2018a: 41.
Material examined.
SAUDI ARABIA: 1 ♂, Riyadh, El Ha’ir, 16–21.IV.1980, K.M. Guichard (NHMUK 013380449).
Distribution.
*Saudi Arabia; Central Asia, Kazakhstan, China (Gansu).
Sphecodes villosulus
Schwarz, 2010
D12FCFAA24895241B1E7149122E79AA7
Sphecodes villosulus Schwarz, 2010: 486–491, ♀, ♂ (holotype: ♀, United Arab Emirates, Dubai, Nakhalai, 28–30.IV.1984, in Malaise trap, E. Sugden leg.; BLCU).
Diagnosis.
This species differs from other small Palaearctic species with 5–6 hamuli in the hind wing by having a unique combination of simple mandibles and the male gonocoxite dorsally with an impression. The female is closest to S. armeniacus owing to dense appressed snow-white pubescence obscuring the integument on face, a transverse head and sparsely punctate mesoscutum, but differs from this species by sparser and finer punctate ocello-ocular area (3–5 μm / 2–3 versus 5–10 μm / 1–2) and strongly transverse F3 (almost square in S. armeniacus). The male of S. villosulus recalls S. miniatus in the rectangular gonostylar shape, but clearly differs from this species by the less developed tyloids on the flagellomeres extending to approximately a half of ventral flagellar surfaces (versus those across 4/5).
Material examined.
UNITED ARAB EMIRATES: 1 ♀, 1♂, Abu Dhabi, 30.I.1987, I. Hamer (NHMUK 013380419, 013380423); 1 ♀, 2♂♂, Abu Dhabi, 31.III.1987 (NHMUK 013380418, 013380421, 013380420); 1 ♀, idem, 10.IV.1987, I. Hamer (NHMUK 013380422); 1 ♀, Hatta, 20.XII.1990 (NHMUK 013380424); 2 ♂♂, idem, 23.VIII.1991 (NHMUK 013380426, 013380427); 1 ♀, idem, 5.III.1993, I. Hamer (NHMUK 013380425); 3 ♀♀, North Ras, Al Khaimah, 17.II.2018 (M. Mokrousov) (ZISP); SAUDI ARABIA: 1 ♀, Riyadh, El Ha’ir, 19.III.1980, K.M. Guichard (NHMUK 013380448); OMAN: 1 ♀, Rostaq, 350 m, 21–31.III.1976, K.M.Guichard (NHMUK 013380444).
Published records.
Schwarz 2010: 486 (United Arab Emirates); Ascher and Pickering 2019 (United Arab Emirates).
Distribution.
United Arab Emirates, *Oman, *Saudi Arabia.
Discussion
In total, 26 species of Sphecodes are recorded from the Arabian Peninsula and surrounding lands (Israel, Jordan and Syria) (Table 1). This is a comparable number to the Iranian fauna, but distinctly less in comparison with the adjacent fauna of Turkey, North Africa and Central Asia (Table 3).
Table 3.
List of Sphecodes species recorded in Arabian Peninsula and surrounding lands (AP+SL), Turkey, Iran, North Africa (Morocco, Algeria, Libya, Tunisia, Egypt) and Central Asia (Kazakhstan, Kyrgyzstan, Uzbekistan, Turkmenistan, Tajikistan).
Sphecodes species | AP+SL | Turkey | Iran | North Africa | Central Asia | |
1 | S. albilabris (Fabricius, 1793) | – | + | + | + | + |
2 | S. alternatus Smith, 1853 | + | + | + | + | + |
3 | S. anatolicus Warncke, 1992 | – | + | + | – | + |
4 | S. armeniacus Warncke, 1992 | – | + | – | + | + |
5 | S. atlanticus Warncke, 1992 | + | – | – | + | – |
6 | S. atlassa Warncke, 1992 | – | – | – | + | – |
7 | S. barbatus Blüthgen, 1923 | + | + | – | – | – |
8 | S. crassanus Warncke, 1992 | – | + | – | – | + |
9 | S. crassus Thomson, 1870 | – | + | + | + | + |
10 | S. cristatus Hagens, 1882 | – | + | – | – | + |
11 | S. croaticus Meyer, 1922 | – | + | + | + | + |
12 | S. dathei Schwarz, 2010 | + | – | – | – | – |
13 | S. dusmeti Blüthgen, 1924 | + | + | – | + | – |
14 | S. ebmeri Astafurova & Proshchalykin, 2018 | – | – | + | – | – |
15 | S. ephippius (Linné, 1767) | + | + | + | – | + |
16 | S. ferruginatus Hagens, 1882 | – | + | – | – | + |
17 | S. geoffrellus (Kirby, 1802) | – | + | – | + | + |
19 | S. gibbus (Linnaeus, 1758) | + | + | + | + | + |
20 | S. hakkariensis Warncke, 1992 | – | + | – | – | + |
21 | S. haladai Warncke, 1992 | – | – | + | + | + |
22 | S. hyalinatus Hagens, 1882 | – | – | – | – | + |
23 | S. hirtellus Blüthgen, 1923 | – | – | – | + | – |
24 | S. intermedius Blüthgen, 1923 | + | + | – | + | + |
25 | S. longulus Hagens, 1882 | + | + | + | – | + |
27 | S. longuloides Blüthgen, 1923 | + | – | – | + | – |
28 | S. majalis Pérez, 1903 | + | + | + | + | – |
29 | S. marginatus Hagens, 1882 | + | – | – | + | – |
30 | S. monilicornis (Kirby, 1802) | + | + | + | + | + |
31 | S. niger Hagens, 1874 | – | + | – | – | – |
32 | S. nomioidis Pesenko, 1979 | + | + | – | – | – |
33 | S. nurekensis Warncke, 1992 | – | – | – | – | + |
34 | S. olivieri Lepeletier de Saint Fargeau, 1825 | + | + | + | + | + |
35 | S. pectoralis Morawitz, 1876 | – | – | + | – | + |
36 | S. pellucidus Smith, 1845 | + | + | + | + | + |
37 | S. pesenkoi Astafurova & Proshchalykin, 2018 | – | – | – | – | + |
38 | S. pinguiculus Pérez, 1903 | + | + | + | + | + |
39 | S. pseudofasciatus Blüthgen, 1925 | – | + | – | + | – |
40 | S. puncticeps Thomson, 1870 | + | + | + | + | + |
41 | S. reticulatus Thomson, 1870 | – | + | + | – | + |
42 | S. rubicundus Hagens, 1875 | + | + | + | – | – |
43 | S. rubripes Spinola, 1839 | + | – | – | + | – |
44 | S. ruficrus (Erichson, 1835) | + | – | – | + | – |
45 | S. rufiventris (Panzer, 1798) | + | + | + | + | + |
46 | S. sandykachis Astafurova & Proshchalykin, 2018 | – | – | – | – | + |
47 | S. saxicolus Warncke, 1992 | – | – | + | – | + |
48 | S. scabricollis Wesmael, 1835 | – | + | + | – | + |
49 | S. schenckii Hagens, 1882 | + | + | + | – | – |
50 | S. schwarzi Astafurova & Proshchalykin, 2015 | – | – | – | – | + |
51 | S. spinulosus Hagens, 1875 | – | + | + | + | + |
52 | S. tadschicus Blüthgen, 1935 | + | + | + | – | + |
53 | S. trjapitzini Astafurova & Proshchalykin, 2018 | – | – | – | – | + |
54 | S. turanicus Astafurova & Proshchalykin, 2017 | + | – | – | – | + |
55 | S. zangherii Noskiewicz, 1931 | – | + | – | – | – |
56 | S. villosulus Schwarz, 2010 | + | – | – | – | – |
Total: | 26 | 34 | 25 | 26 | 35 |
The distribution of Sphecodes species are given according to Özbek et al. 2015 (Turkey), Astafurova et al. 2018d (Iran), Warncke 1992 (North Africa), Astafurova and Proshchalykin 2017b and Astafurova et al. 2018a, c (Central Asia).
The Sphecodes fauna of the Arabian Peninsula and surrounding lands is a complex of Mediterranean, Sahara-Gobian, endemic, and species widespread in the Palaearctic region. Eight species, namely S. alternatus, S. ephippius, S. gibbus, S. longulus, S. monilicornis, S. marginatus, S. pellucidus, and S. puncticeps are widespread from north to south of the Palaearctic region and occur in biomes ranging from forest to desert. However, two of these (S. marginatus and S. puncticeps) are recorded from the Arabian Peninsula and the remainder all are found only in Mediterranean areas.
Sphecodes majalis, S. schenckii Hagens, S. rubicundus, and S. nomioidis are steppe species, distributed in Europe, Turkey and the Caucasus to Iran. Of them, only S. nomioidis is recorded from the Arabian Peninsula.
Sphecodes olivieri, S. intermedius, S. rufiventris, and S. pinguiculus are widespread from steppe to desert in the Western Palaearctic. Of these only S. rufiventris is not recorded from the Arabian Peninsula.
Sphecodes barbatus, S. rubripes, and S. ruficrus are possibly purely Mediterranean species not reaching the Arabian Peninsula. In contrast, S. atlanticus turns out to be Sahara-Arabian. Sphecodes dusmeti and S. longuloides are Mediterranean-Arabian species.
Sphecodes tadschicus and S. turanicus are Irano-Turanian species reaching the Arabian Peninsula.
Finally, two species, S. dathei and S. villosulus are endemic to the Arabian Peninsula.
Although the Arabian fauna of the genus is not fully studied it is now clear that the Arabian fauna differs from that of the Mediterranean; of 26 recorded species only six (S. olivieri, S. intermedius, S. marginatus, S. nomioidis, S. pinguiculus, and S. puncticeps) are common to both and these are all widespread in the Western Palaearctic.
Supplementary Material
Acknowledgments
We are grateful to Fritz Gusenleitner (OLBL) for help during our visit to Austria, and Andrew Grace (Hastings, UK) for checking the English. We thank Hege Vårdal (NHRS), Lukasz Przybylowicz (ISZP), Michael Ohl, and Viola Richter (ZMHB) for providing Sphecodes type specimens. We also thank Michael Engel, Petr Bogusch, and anonymous reviewer for their comments and suggestions to streamline and improve the earlier drafts of the manuscript.
This investigation was supported by the Russian Funds for Basic Research (grant numbers 17-04-00259 and 19-04-00027) and the state research project (№ АААА-А19-119020690101-6).
Citation
Astafurova YuV, Proshchalykin MYu, Schwarz M (2019) The distribution of the genus Sphecodes Latreille (Hymenoptera, Halictidae) of the Arabian Peninsula and surrounding countries with description of hitherto unknown female of S. atlanticus Warncke, 1992 and male of S. dathei Schwarz, 2010. ZooKeys 872: 13–40. https://doi.org/10.3897/zookeys.872.35361
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