Research Article |
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Corresponding author: Gideon Pisanty ( gidpisa79@yahoo.com ) Academic editor: Brendon Boudinot
© 2025 Gideon Pisanty, Rémi Santerre, Teresa Martin, Sophie Cardinal, Thomas J. Wood.
This is an open access article distributed under the terms of the CC0 Public Domain Dedication.
Citation:
Pisanty G, Santerre R, Martin T, Cardinal S, Wood TJ (2025) Integrated taxonomic revision of the mining bee subgenus Andrena (Micrandrena) (Hymenoptera: Andrenidae) in the Levant and Cyprus. Arthropod Systematics & Phylogeny 83: 573-655. https://doi.org/10.3897/asp.83.e166986
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Andrena (Micrandrena) Ashmead is the largest subgenus of Andrena Fabricius 1775, with more than 150 species distributed throughout the northern hemisphere. The subgenus has gained notoriety as one of the most difficult taxonomic groups of bees, and remains poorly studied across large parts of the Palaearctic region. Based on extensive collecting in Israel, Lebanon and Cyprus, together with efficient DNA barcoding and and re-examination of old museum material, we present a thorough revision of the species of A. (Micrandrena) occuring in the region of the Levant (Israel, the West Bank, Jordan, Lebanon and Syria) and the island of Cyprus, including a detailed identification key, and a summary of our knowledge of the distribution, phenology and foraging biology of each taxon. Our study enumerates forty-two species of Andrena (Micrandrena) from the Levant and Cyprus, including four species new to the region, and nine species new to science: Andrena aphroditae Pisanty sp. nov., A. alshaykh Pisanty sp. nov., A. aspera Pisanty & Wood sp. nov., A. chananaea Pisanty & Wood sp. nov., A. friedmani Pisanty sp. nov., A. hebraica Pisanty & Wood sp. nov., A. kugleri Pisanty sp. nov., A. libanica Wood sp. nov., and A. phoenicia Pisanty sp. nov. We describe the males of A. calandra Warncke, 1975 and A. lindbergella Pittioni, 1950 for the first time. We additionally synonymise Andrena dargia Warncke, 1965 with A. minutula (Kirby, 1802) syn. nov., and recognise two previously subspecific names as valid species: Andrena leptura Warncke, 1974 stat. nov. and A. povolnyi, 1974 Warncke stat. nov.
DNA barcoding, Eastern Mediterranean, Israel, Jordan, Lebanon, solitary bee, species key, Syria
Andrena (Micrandrena) Ashmead is the largest subgenus of Andrena Fabricius 1775, itself being the second largest genus of bees after Lasioglossum (Ascher & Pickering 2025;
Because of their small size and difficulty to recognize in the field, the life history of many species is poorly known. From the better-studied species, it appears that many are pollen generalists, meaning that plant associations also cannot help with species identification (
The taxonomic circumscription of the subgenus Andrena (Micrandrena) has seen some changes over the years. Most importantly, in an attempt to create stable monophyletic subgeneric divisions, a recent large-scale molecular phylogenetic study has broadened the traditional scope of the subgenus, to include also the groups known as Distandrena Warncke, Fumandrena Warncke, and Proxiandrena Schmid-Egger (
While Andrena (Micrandrena) have been heavily studied in Western and Central Europe, even historically (e.g.
Body length was measured in lateral view to the nearest 0.5 mm, as the sum of distances from the antennal sockets to the posterior end of the propodeum and from the latter to the tip of the metasoma. For convenience, we followed some European forewing venation terms (e.g. Gusenleitner & Schwarz 2002) as follows: the vein separating the first and second cubital cells of the forewing (cu-v in Michener 1944) is referred to here as the nervulus. The nervulus is described as antefurcal, interstitial, or postfurcal, if its anterior end is situated proximal to, in alignment with, or distal to the posterior end of the basal vein, respectively. Other morphological terms follow
DNA barcoding of the COI mitochondrial gene was conducted as specified in
Specimen depositories are listed under the following acronyms: AV – Private collection of Androulla Varnava, Limassol, Cyprus;
At the subgeneric level, the results of the phylogenetic analysis (Fig.
Maximum Likelihood tree of representative COI barcodes of Andrena (Micrandrena) from the Levant and Cyprus together with some closely related taxa, inferred using IQ-TREE with 1000 ultra-fast bootstraps. Bootstrap values below 70 are not shown. The janthina, longibarbis, minutula and oedicnema species groups are shaded in yellow, red, blue and green, respectively. Each sequence is annotated with its BOLD accession number (except for the NUMT sequence), followed by the species name, sex, three-letter country code, and collection locality.
Our phylogenetic analysis also broadly concurs with the inner division of subgenus Micrandrena found in
At the species level, four taxa exhibited significant intraspecific distances across their geographical ranges in our tree (Fig.
In total, 42 species of Andrena (Micrandrena) are identified from the region of the Levant and Cyprus, 36 of which are represented by molecular barcodes. Thirty-three species are reported from Israel, 24 from Lebanon, 16 from the West Bank, 18 from Syria, 19 from Jordan, and 5 from Cyprus. Nine species are newly described for science, four are new for the region, and six are removed from the regional list. Detailed accounts of all taxa follow, arranged by species groups.
Micrandrena Ashmead, 1899: 89. Type species: Micrandrena pacifica Ashmead = Andrena melanochroa Cockerell, 1898, by original designation.
Andrenella
Hedicke, 1933: 210. Type species: Melitta minutula Kirby, 1802, by original designation. Syn.
Distandrena
Warncke, 1968a: 60. Type species: Andrena longibarbis Pérez, 1895, by original designation. Syn.
Fumandrena
Warncke, 1975a: 57. Type species: Andrena fumida Pérez, 1895, by original designation. Syn.
Proxiandrena
Schmid-Egger, 2005: 1030. Type species: Melitta proxima Kirby, 1802 = Andrena proxima, by original designation. Syn.
As a unified group, Andrena (Micrandrena) are too morphologically diverse to diagnose with unique defining characters, especially with regard to other members of the highly diverse clade of small-sized Andrena distributed primarily in the Old World (clades 23–24 in
For the sake of the present discussion and for utility within the fauna of the Levant and Cyprus, we divide the Palaearctic members of A. (Micrandrena) into the following groups, which to our best understanding, correspond to distinct clades in phylogenomic analysis (
1. Andrena longibarbis group – former subgenus Distandrena.
2. Andrena minutula group – this is the old concept of subgenus Micrandrena sensu Warncke in the Palaearctic but excluding the species around A. oedicnema Warncke and A. proxima (Kirby). This group contains the bulk of the species diversity of the subgenus. It corresponds to Schmid-Egger & Scheuchl’s minutula- and nana-groups combined (Schmid-Egger & Scheuchl 1997). We see no justification to distinguish the nana group here, as preliminary molecular data does not support its monophyly, and the minutula/nana group division is not clearly applicable outside Central Europe.
3. Andrena oedicnema group – A. oedicnema Warncke and the closely related A. cedricola Wood.
4. Other unassigned, peculiar taxa, including the well-known Andrena proxima group, here represented by a single species only.
The Andrena longibarbis group can be well characterized against other Andrena subgenera by the combination of: 1. A clypeus that is completely flat or almost so, often with longitudinal striations (Fig.
The highly diverse Andrena minutula group is more variable morphologically compared to the A. longibarbis group, but it is characterized most of all by a propodeal triangle that is finely but strongly rugose to rugose-areolate, at least on the basal half (Fig.
Most of the remaining taxa of A. (Micrandrena) in the treatment below can also be diagnosed against other subgenera based on the same criteria mentioned above. Hence, most of the characters of the Andrena minutula group apply also to the A. oedicnema group and to A. proxima; A. extenuata Wood also possesses a similar strongly rugose propodeal triangle. The A. oedicnema group is further characterized by mirror-smooth, mostly impunctate terga (Fig.
It is important to note that several species of the A. minutula group occur in two generations which are morphologically distinct. This includes A. alfkenella Perkins, A. alfkenelloides Warncke, A. chananaea Pisanty & Wood sp. nov., A. minutula, and A. minutuloides Perkins. As a general rule, the second generations possess a smoother cuticle and brighter pubescence (particularly the male facial pubescence), which are most likely adaptations for the warmer ambient temperature and stronger solar radiation associated with late season (
Most of the bionomic data on Micrandrena species has been gathered from studying Central European taxa, especially the work of
In terms of biogeography, the highly diverse Andrena minutula group is common in temperate and Mediterranean biomes throughout the Palaearctic, with numerous species confined to higher elevations. The Andrena oedicnema group is associated with similar habitats, with a much more limited distribution. On the other hand, the A. longibarbis group is strongly associated with dry habitats in the Western Palaearctic, and is most diverse around the southern Mediterranean Basin and the Iberian Peninsula.
Andrena decollata
Warncke, 1974b: 13, 40, ♀♂ [Algeria:
Coastal habitats along the south Mediterranean. In the Levant, limited to Israel’s coastal plain, likely extending into Lebanon (
Mid-January to late April.
Collected from Brassicaceae (Brassica) and Boraginaceae (Alkanna).
ISRAEL ● 1♂; Binyamina; 26 Jan. 1976; A. Freidberg leg.; SMNHTAU 348576 ● 1♂; Gan Soreq, Giv’at Humra; 31°56’07” N 34°44’35” E; 25 m a.s.l.; 4 Feb. 2020; L. Friedman leg.; SMNHTAU 330935 ● 1♀; Gvulot; 14 Mar. 1987; E. Shney-Dor leg.; SMNHTAU 348575 ● 1♀; Hof Dor–HaBonim N.R. [Nature Reserve]; 32.638–43° N 34.922–8° E; 2 Mar. 2025; L. Friedman leg.; SMNHTAU ● 2♂; Hof Rosh Haniqra N.R.; 33.076–85° N 35.105–9° E; 18 Mar. 2025; G. Pisanty leg.; SMNHTAU 465053, 465054 ● 1♀; Hof Rosh Haniqra N.R., nr. Hof Bezet; 18 Mar. 2025; L. Friedman leg.; SMNHTAU 464993 ● 1♂; Hulon; 18 Jan. 1954; L. Fishelsohn leg.; SMNHTAU 348577 ● 1♀; Mikve-Jisrael B G [Botanical Garden]; 15 Mar. 1946; SMNHTAU 348588 ● 1♀; Nahal Alexander; 27 Feb. 2020; K. Levy leg.; BOLD accession no. ANDIL485-25; SMNHTAU 337969 ● 1♀; ibid.; BOLD accession no. ANDIL105-22; SMNHTAU 337967 ● 1♀; ibid.; 29 Mar. 2021; on Brassica tournefortii; SMNHTAU 380253 ● 1♀; ibid.; 3 Apr. 2021; SMNHTAU 379996 ● 1♀; Nahal Alexander NP [National Park]; 32.3955° N 34.8755° E; 25 Feb. 2024; G. Pisanty leg.; SMNHTAU 448453 ● 6♂; ibid.; SMNHTAU 448449 to 448452, 448454, 448455 ● 1♂; Netanya, Irus Ha’Argaman NR; 24 Feb. 2021; ITI Bee Course leg.; SMNHTAU ● 1♀; Nir Eliyahu; 14 Apr. 2023; S. Asis leg.; SMNHTAU 414787 ● 3♂; Nizzanim, D6; 17 Feb. 2005; A. Freidberg leg.; SMNHTAU ● 1♀; Nizzanim Nature Reserve; 25 Feb. 2009; L. Friedman leg.; BOLD accession no. ANDIL110-22; SMNHTAU 348583 ● 2♂; ibid.; SMNHTAU 348581, 348582 ● 1♂; Nizzanim Nature Reserve, Nahal Evtah; 25 Feb. 2009; A. Freidberg leg.; SMNHTAU 348580 ● 2♂; Or ‘Aqiva, 1km E; 32.493° N 34.934° E; 33 m a.s.l.; 2 Mar. 2025; G. Pisanty leg.; SMNHTAU 464087, 464088 ● 2♂; ibid.; L. Friedman leg.; SMNHTAU 464107, 464108 ● 1♀; Qadima; 25 Mar. 2009; A. Dorchin leg.; SMNHTAU ● 1♀; R.Gn [?Ramat Gan]; 3 Feb. [19]40; SMNHTAU 348586 ● 1♀; ibid.; 6 Feb. [19]40; SMNHTAU 348587 ● 3♀; Rehobot [Rehovot]; 9 Feb. 1942; H. Bytinski-Salz leg.; SMNHTAU 348589 to 348591 ● 3♀; Rehoboth; [??] Feb. [19]34; Hecht leg.; SMNHTAU 348593 to 348595 ● 1♂; ibid.; SMNHTAU 348592 ● 1♂; Sde Uziyahu; 31.753° N 34.667° E; 13 Mar. 2023; E.L.A.E. leg.; pan trap; SMNHTAU 462968 ● 1♂; T.A.g [?Tel Aviv Botanical Garden]; 4 Feb. [19]40; SMNHTAU ● 1♀; Tel Aviv; 17 Mar. 1940; H. Bytinski-Salz leg.; SMNHTAU 348584 ● 1♂; ibid.; [??] Mar. 1940; SMNHTAU 348585 ● 2♀; Tel Aviv, Ramat Aviv; 32.130° N 34.801° E; 9 Feb. 2015; G. Pisanty leg.; pan trap; SMNHTAU 203163, 203164 ● 2♂; ibid.; SMNHTAU 203161, 203162 ● 1♂; ibid.; 1 Apr. 2017; on Brassicaceae; SMNHTAU 270430 ● 1♂; Zur Moshe; 27 Apr. 2015; I. Eliakim leg.; SMNHTAU 185879. – TUNISIA ● 1♀; Djerba Midoun [2 km S of Sedouikech, Mosquée el louttaa Souterraine de Sedouikech]; 26 Feb. 2023; N.J. Vereecken leg.; BOLD accession no. WPATW1341-23; TJWC.
Andrena govinda
Warncke, 1974b: 14, 41, ♀♂ [Egypt:
Andrena govinda ssp. eremitica
Warncke, 1974b: 14, 41, ♀♂ [Tunisia:
Desert habitats in north Africa and the Levant (southern Israel, Jordan*, Syria*,
Early February to late April.
Collected from Brassicaceae (Diplotaxis, Erucaria, Zilla) and Nitrariaceae (Nitraria).
HOLOTYPE: EGYPT ● ♀; Wadi Digla; 12 Feb. 1932; H. Priesner leg.;
Andrena herodesi
Pisanty & Wood, 2022:
Endemic to arid habitats in the southern Levant (southern Israel, West Bank, Jordan).
March.
None.
Male unknown.
HOLOTYPE: WEST BANK ● ♀; “ISRAEL, Herodyon” [Herodium]; 31°40’ N 35°14’ E; 31 Mar. 2009; M. Guershon leg.; SMNHTAU 348536. – PARATYPES: ISRAEL ● 2♀; Sede Boqer; 21 Mar. 1985; I. Yarom leg.; SMNHTAU 207231, 348532. – JORDAN ● 1♀; Wadi-el-Mawjib; 400 m a.s.l.;, 20 Mar. 2009; V. Barták leg.;
Named after the Israeli entomologist Jehoshua Kugler (1916–2007).
Within the Andrena longibarbis species group, A. kugleri belongs to the species around A. mariana Warncke, which are characterized by a largely non-rugose clypeus. Among these species, A. kugleri can be diagnosed by the combination of the relatively narrow female labral process (Fig.
FEMALE. Body length: 6–7 mm. — Integumental colour: Body black. Flagellum brown anteriorly, occasionally with weak reddish hue. Legs black to brown. Wings hyaline, veins and stigma golden (Fig.
In a broad sense, Andrena kugleri is endemic to Israel, the West Bank and southern Lebanon. The principal distribution is in desert areas of southern Israel and the West Bank, while the species is absent from most of the Mediterranean region of Israel. However, a disjunct population exists on both sides of the Israeli-Lebanese border, where annual precipitation exceeds 600 mm. This population is known only from females, and the single available barcode (from Lebanon) is 13% different from the main population. Males should be located and examined to conclude whether this population represents a separate taxon. The species is also known from only two localities in the central coastal plain, one of these is the old botanical garden in southern Tel Aviv, where a great proportion of the type material has originated. A single specimen with a label from Turkey in Warncke’s handwriting is of dubious origin, as noted by Warncke himself. More DNA barcoding is needed to better assess the uniformity of this taxon across its range.
Mid-February to mid-April, up to early May in southern Lebanon.
Collected from Brassicaceae (Erucaria, Sisymbrium, etc.) and Asparagaceae (Scilla).
In his collection, Warncke labeled this taxon A. mariana progressa Warncke, an unpublished name which adds to his multiple subspecific concepts of A. mariana, all of which are now considered distinct species or junior synonyms of other distinct species (
Andrena kugleri is very similar to A. rubecula known from nearby Egypt, and female specimens collected near the southernmost part of the Israeli-Egyptian border (previously classified as A. rubecula,
HOLOTYPE: WEST BANK ● 1♀; “ISRAEL, Jericho” [Jericho]; [approx. 31.86° N 35.46° E]; [approx. –250 m a.s.l.]; 13 Feb. 1975; F. Kaplan leg.; SMNHTAU 373036. – PARATYPES: ISRAEL ● 1♀; Avedat; 13 Apr. 1990; Kl. Warncke leg.;
(A. rubecula Warncke): HOLOTYPE: EGYPT ● ♀; Meadi [Maadi]; 20 Feb. 1931; H. Priesner leg.;
Andrena mariana ssp. leptura
Warncke, 1974b: 13, 40, ♀♂ [Egypt:
Desert habitats in the south-east Mediterranean. Newly reported from the Levant*, in southern Israel*.
Mid-January to mid-April.
Collected from Brassicaceae (Diplotaxis, Zilla).
Molecular barcodes strongly suggest that this taxon is distinct (Fig.
ISRAEL ● 2♀,1♂; Arava, 4 km W of Hazeva; 19–29 Feb. 1988; R. Leys leg.;
Andrena longibarbis
Pérez, 1895: 45, ♀♂ [Tunisia:
Andrena trizona
Pérez, 1895: 45, ♀ [SE Algeria: ?
Shrublands, warm grasslands, and semi-deserts in the southern Mediterranean and the Iberian Peninsula. In the Levant, limited to southern Israel and the West Bank* (
February to mid-April; in Iberia up to mid-May (
Broadly oligolectic on Brassicaceae (
EGYPT ● 1♀; Alexandria, Montaza; 11 Apr. 1983; K.M. Guichard leg.;
Andrena mariana
Warncke, 1968b: 75, ♀♂ [Canary Islands:
South Mediterranean (
Mid-February to late April.
Collected from Brassicaceae.
See A. leptura stat. nov. and A. kugleri sp. nov.
ISRAEL ● 1♀,1♂; 10 km W Dimona; 403 m a.s.l.; 20 Mar. 2012; A. Dorchin leg.; TJWC ● 2♀; Holot Mash’abbim; 30.999° N 34.7575° E; 13 Feb. 2022; L. Friedman leg.; SMNHTAU 384379, 384380 ● 2♂; ibid.; SMNHTAU 384376, 384385 ● 1♂; ibid.; 30.999° N 34.7578° E; G. Pisanty leg.; sweeping; SMNHTAU 384335 ● 2♀; ibid.; 18 Feb. 2022; SMNHTAU 384502, 384541 ● 3♂; ibid.; SMNHTAU 384508, 384510, 384533 ● 1♂; ibid.; BOLD accession no. ANDIL498-25; SMNHTAU 384505 ● 2♀; ibid.; pan trap; SMNHTAU 384611, 384612 ● 1♀; ibid.; BOLD accession no. ANDIL499-25; SMNHTAU 384610 ● 1♀; Holot Shunera; 30.941° N 34.597° E; 17 Mar. 2017; G. Pisanty leg.; pan trap; BOLD accession no. ANDIL439-25; SMNHTAU 269102 ● 1♀; KKL Park Sayeret Shaqed; 31.2795° N 34.6495° E; 19 Mar. 2022; G. Pisanty leg.; sweeping; BOLD accession no. ANDIL503-25; SMNHTAU 385879 ● 3♀; Mashabe Sade; 16 Feb. 1976; A. Freidberg leg.; SMNHTAU 348560 to 348562 ● 1♀; Nahal Zin; 16 Mar. 2008; Y. Hollander leg.; SMNHTAU 19223 ● 1♀; Shivta; 13 Mar. 1977; A. Freidberg leg.; SMNHTAU 348566 ● 3♀; ibid.; 17 Mar. 1977; SMNHTAU 348563 to 348565 ● 1♀; Subeita [Shivta]; 21 Mar. 1946; SMNHTAU. – JORDAN ● 7♀; Jordan E., Azraq; 24 Apr. 1996; Marek Halada leg.;
Andrena alfkenella
Perkins, 1914: 112–113, ♀♂ [England:
Andrena moricella
Perkins, 1914: 113, ♂ [England:
Andrena alfkenella ssp. sunna
Warncke, 1975b: 295, ♀♂ [Spain:
Mostly mesic habitats in Morocco, Europe and the northwestern Middle East. In the Levant, limited to mountains above 1300 m in north and central Lebanon (
Late April at least until mid-July (in Europe until August), in two generations.
Polylectic. Pollen hosts include Apiaceae, Brassicaceae, Plantaginaceae and Rosaceae (
LEBANON: See
Andrena alfkenelloides ssp. cardalia
Warncke, 1975a: 47, ♀♂ [SE-Turkey:
Shrublands, sub-alpine and semi-arid habitats in Cyprus, all countries of the Levant, and southern Turkey.
Late January to early June, in two generations.
Collected mostly from Asteraceae (Anthemis, Calendula, Crepis, Glebionis, Helichrysum, Senecio) and Brassicaceae (Alyssum, Isatis, Lepidium, Sinapis), also from Apiaceae, Caryophyllaceae, Geraniaceae, Liliaceae and Rosaceae.
The status of A. a. cardalia is not sufficiently clear at this point, as preliminary results suggest that the nominate form of A. alfkenelloides might be closer to A. floricola Eversmann than to the eastern subspecies. Barcodes of the nominate form from Greece are required to fully assess the status of this species complex, and to conclude whether eastern populations constitute a distinct taxon.
HOLOTYPE: TURKEY ● 1♀; Anatolia, Antakya; 1–7 Jun. 1965; J. Gusenleitner leg.;
A. alfkenelloides Warncke s.s.: HOLOTYPE: GREECE ● 1♀; Trikala; 17 Apr. 1962; Kl. Warncke leg.;
Named after the Arabic name of Mount Hermon, Jabal al-Shaykh (‘Mountain of the Sheikh’). The species epithet is a noun in apposition.
Within the Andrena minutula species group, A. alshaykh belongs to the species around A. rugulosa Stöckhert, characterized by a smooth clypeus and punctate terga, which include also A. lindbergella Pittioni and A. libanica Wood sp. nov. It is closest to A. lindbergella Pittioni from Cyprus, and until the discovery of the distinct male of A. lindbergella, they were considered conspecific. The female differs from A. lindbergella in the tergal discs which are more strongly shagreened and more obscurely punctured (Fig.
FEMALE. Body length: 6.5–7.5 mm. Integumental colour: Body and legs black. Anterior side of flagellum greyish-black to slightly reddish. Apical tarsomeres brown. Wings weakly infuscate, veins brown, stigma brown peripherally, reddish centrally (Fig.
Sub-alpine habitats in northern Israel (Mt. Hermon) and Lebanon, likely also Syria, above 1900 m. Previously reported from Israel and Lebanon as A. lindbergella (
Mid-May to early July.
Collected from Brassicaceae (Alyssum).
HOLOTYPE: ISRAEL ● 1♀; Har Hermon [Mount Hermon]; [approx. 33.315° N 35.810° E]; 2200 m a.s.l.; 27 May 1999; A. Freidberg leg.; SMNHTAU. – PARATYPES: ISRAEL ● 2♀; ‘Emeq Eshhar, Plot E7; 33.304° N 35.790° E; 2048 m a.s.l.; 21 Jun. 2019; A. Dorchin & T. Roth leg.; SMNHTAU 309522, 309523 ● 1♀; Har Hermon; 2200 m a.s.l.; 27 May 1999; A. Freidberg leg.; SMNHTAU ● 1♀; Har Hermon; 33.3027° N 35.7855° E; 2020 m a.s.l.; 15 May 2016; G. Pisanty leg.; SMNHTAU 242148 ● 1♀; ibid.; BOLD accession no. ANDIL247-22; SMNHTAU 242147 ● 1♀; ibid.; 33.304° N 35.7875° E; SMNHTAU 242308 ● 3♀; Har Hermon; 33.309° N 35.792° E; 1950 m a.s.l.; 15 May 2016; G. Pisanty leg.; pan trap; SMNHTAU 242178 to 242180 ● 1♂; ibid.; SMNHTAU 242183 ● 1♂; ibid.;
Named after the Greek goddess Aphrodite, who is strongly associated with the island of Cyprus.
Within the Andrena minutula species group, A. aphroditae belongs to the species around A. spreta Pérez, which are characterized in the female by a clypeus which is non-rugose, weakly domed and partly to fully shagreened, a scutum which is shagreened to partly smooth, with fine, relatively sparse punctures, and terga which are mostly shagreened and impunctate. In the Levant and Cyprus, these include A. hebraica Pisanty & Wood sp. nov., A. minutuloides Perkins, A. spreta, A. tiaretta Warncke, and A. tkalcui Gusenleitner & Schwarz. Female Andrena aphroditae are distinguished from A. hebraica and A. tiaretta by the scutum and scutellum which are usually somewhat shiny and distinctly punctured (completely dull in A. hebraica; dull and weakly punctured in A. tiaretta; Figs
Female. Body length: 5–6.5 mm. Integumental colour: Body and legs black. Flagellum black, distal flagellomeres increasingly covered with minute greyish setae. Distal tarsomeres black to dark brown. Wings weakly infuscate, veins dark brown, stigma centrally dark to light brown (Fig.
Endemic to Mediterranean shrublands in Cyprus.
Mid-February to mid-April.
Collected from Asteraceae (Glebionis, Helichrysum), Brassicaceae (Sinapis), Cistaceae (Cistus) and Lamiaceae (Lavandula).
HOLOTYPE: CYPRUS ● 1♀; Pano Panagia env.; 34.921–928° N 32.631–640° E; [700–850 m a.s.l.]; 15 Apr. 2025; G. Pisanty leg.; SMNHTAU 467594. – PARATYPES: CYPRUS ● 1♀; Agia Erini; 11 Apr. [19]37; Mavromoustakis leg.; SMNHTAU ● 2♀; Akamas Pen.; 35.018–031° N 32.34–36° E; 7 Apr. 2025; G. Pisanty leg.; SMNHTAU 466866, 466867 ● 1♀; Akamas Pen.; 35.019–26° N 32.326–52° E; 8 Apr. 2025; G. Pisanty leg.; SMNHTAU 467010 ● 3♂; Larnaca [District], Larnaca Salt Lake; 1 m a.s.l.; 18 Feb. 2025; R. Santerre leg.; UMONS ● 2♂; Limassol [District], Anogyra; 468 m a.s.l.; 27 Mar. 2025; ibid. ● 4♀,3♂; Limassol, Arakapas, 2 km W from village; 454 m a.s.l.; 8 Mar. 2025; ibid. ● 1♂; Limassol, Palódia, Ayia Irini Monastry; 34.7441° N 32.976° E; 192 m a.s.l.; 7 Mar. 2024; R. Santerre leg.; on Sinapis alba; BOLD accession no. RSCMC032-25; UMONS ● 3♂; Limassol, Palodia, SE village; 257 m a.s.l.; 8 Mar. 2025; R. Santerre leg.; UMONS ● 1♀; Limassol, Parekklisia, 5 km N from village; 243 m a.s.l.; 14 Mar. 2025; ibid. ● 1♂; Moniatis; 34.870–82° N 32.877–92° E; 9 Apr. 2023; G. Pisanty leg.; BOLD accession no. ANDCY037-25; SMNHTAU 426933 ● 2♂; Nicosia [District], Agios Epifanios, 2.5 km S from village; 605 m a.s.l.; 9 Mar. 2025; R. Santerre leg.; UMONS ● 1♂; Nicosia, Agios Ioannis, NW village; 319 m a.s.l.; 9 Mar. 2025; ibid. ● 1♂; Nicosia, Athalassa Forest Park; 165 m a.s.l.; 14 Feb. 2025; ibid. ● 7♂; Nicosia, Lympia, 4 km E from village; 225 m a.s.l.; 14 Feb. 2025; ibid. ● 1♀,1♂; Nicosia, Lythrodontas, 1.5 km N from village; 428 m a.s.l.; 14 Mar. 2025; ibid. ● 1♂; Nicosia, Mosfiloti, 2 km N from village; 197 m a.s.l.; ibid. ● 1♀; Pano Panagia; 34.9213° N 32.6310° E; 15 Apr. 2025; G. Pisanty leg.; pan trap; SMNHTAU 467757 ● 2♂; ibid.; SMNHTAU 467675 ● 2♀,1♂; ibid.;
Nominative feminine singular form of the Latin adjective asper, meaning rough, uneven, coarse, in reference to the species’ integumental sculpturing.
The female of Andrena aspera stands out among Levantine Micrandrena species by the combination of a labral process which is often weakly emarginate apically, distinctly domed clypeus with transverse striations and/or oblique punctures (Fig.
Among Levantine Micrandrena, the male of Andrena aspera is characterized by the combination of a domed, very densely punctured clypeus covered by dense long white hair (Fig.
Female. Body length: 6.5–7.5 mm. — Integumental colour: Body and legs black. Distal flagellomeres brown to black (Fig.
Mediterranean shrublands in Israel, the West Bank and Lebanon. Previously reported from Lebanon as A. simontornyella ssp. corpana (
Mid-February to early April, with rare records until mid-May.
Collected on Apiaceae (Daucus, Ferula, Scandix), Asteraceae (Anthemis, Leontodon) and Brassicaceae (Diplotaxis, Isatis, Sinapis).
HOLOTYPE: ISRAEL ● 1♀; Har Ahino’am [Mount Gilboa, Har Ahino’am]; 32.502–6° N 35.408–14° E; 440 m a.s.l.; 3 Mar. 2025; G. Pisanty leg.; SMNHTAU 463986. – PARATYPES: ISRAEL ● 1♀; Agur; 28 Feb. 2021; A. Eliyahu leg.; SMNHTAU 380374 ● 1♀; Bar’am; 1 Apr. 2016; O. Winberger leg.; SMNHTAU 251858 ● 3♂; Ben Shemen Forest; 31.93° N 34.972° E; 18 Feb. 2017; G. Pisanty leg.; SMNHTAU 268571, 268573, 268574 ● 1♂; ibid.;
Andrena calandra
Warncke, 1975a: 47–48, ♀ [SE Turkey:
The male of A. calandra, similarly to the female, is easily distinguished from other members of the A. minutula group by the combination of a small body size, strong orange colouration of the anterior of the flagellum, polished and mirror-smooth scutum (Fig.
Body length
: 4.5–5.5 mm. — Integumental colour: Head and mesosoma black (Fig.
Shrublands and semi-arid habitats in south-central Turkey and the the Levant* (Northern Israel*, Jordan*).
Late February to early June.
One female collected on Asphodelaceae (Asphodelus).
HOLOTYPE: TURKEY ● ♀; Antakya; 4 Jun. 1965; M. Schwarz leg.;
Andrena cervina
Warncke, 1975a: 52, ♀♂ [Cyprus:
Endemic to Mediterranean shrublands in Cyprus and the Levant (Israel, Lebanon*) (
Available records range from early March to mid-May, but according to IUCN (2025) the season in Cyprus extends up to mid-June.
Females appear to favour Allium spp. (Amaryllidaceae). Collected also on Asteraceae and Brassicaceae.
Levantine populations of Andrena cervina differ from their Cypriot relatives by somewhat weaker and denser scutal punctation, and brighter stigma. We regard these differences as part of the accepted variability within a unified species concept. COI barcodes of the two populations show an average of 2% genetic distance.
CYPRUS ● 11♀; Akamas; 35.02–05° N 32.32–36° E; 9 Apr. 2025; G. Pisanty leg.; on Allium; SMNHTAU 467044 to 467054 ● 6♀,1♂; Akamas, Neo Chorio, Lakki [Latsi]; 100 m a.s.l.; 10 Apr. 2000; J. Vořišek leg.;
Nominative feminine singular form of the Latin adjective chananaeus (=Canaanite).
Within the Andrena minutula species group, the female of A. chananaea is characterized by the combination of a shagreened, strongly punctate clypeus, often with a strong impunctate midline (Fig.
The male of A. chananaea is very hard to diagnose among members of the A. minutula group, due to its extreme morphological variability, both among and within the two seasonal generations. The main consistent characters are a short flagellomere 1, clypeus and scutum which are densely punctured and usually at least partly shagreened, terga which are highly variable but at least weakly punctate, and simple genitalia. The male is closest to A. alfkenella Perkins and A. alfkenelloides cardalia, but exhibits subtle differences in the shape of the genitalia, with the gonostyli only slightly narrowed basally (inner margin of gonostylus more strongly narrowing basally in A. alfkenella and A. a. cardalia), and the penis valves distinctly broader basally vs. apically (more uniformly narrow in the comparison species) (Fig.
First generation female. Body length: 5.5–6 mm. — Integumental colour: Body and legs black. Flagellum black, partly covered by greyish scales especially on distal flagellomeres. Tarsi black to brown. Wings weakly infuscate, veins and stigma brown (Fig.
Shrubland and mesic habitats in all countries of the Levant. Previously reported from Lebanon as A. minutula (
Early February to late June, in two generations (February–mid-April and mid-April–June, depending on elevation).
Collected on Apiaceae (Daucus), Rosaceae (Pyrus) and Sapindaceae (Acer).
HOLOTYPE: ISRAEL ● 1♀; Me’arat Yishah [Mount Carmel, Yishah Cave], 0.5km E; 32.718° N 35.007° E; [310 m a.s.l.]; 22 Feb. 2019; G. Pisanty leg.; BOLD accession no. ANDIL464-25; SMNHTAU 321609. – PARATYPES: ISRAEL ● 2♀; Aqua Bella [Ein Hemed]; 14 May 1951; J. Wahrman leg.; SMNHTAU 353594, 353595 ● 1♀; Biriyya Forest; 32.99–33.00° N 35.52–53° E; 19 May 2023; G. Pisanty leg.; SMNHTAU 429802 ● 1♀; Carmel; 14 Feb. 1976; A. Freidberg leg.; SMNHTAU 353621 ● 1♀; ELA JUN.; [?] Feb. 1984; E. Shney-Dor leg.; SMNHTAU ● 5♀; Har Addir; 33.032–7° N 35.361–72° E; 780–1000 m a.s.l.; 21 May 2025; G. Pisanty leg.; SMNHTAU 470540 to 470544 ● 1♀; Har Addir; 33.033° N 35.361° E; 22 Apr. 2016; G. Pisanty leg.; pan trap; SMNHTAU 240804 ● 1♂; Har Ahino’am; 32.502–6° N 35.408–14° E; 440 m a.s.l.; 3 Mar. 2025; G. Pisanty leg.; SMNHTAU 463954 ● 1♂; Har Avital, Golan Heigh[t] N; 15 Mar. 1995; R. Kasher leg.; SMNHTAU 353476 ● 1♀; Har Dov; 1000 m a.s.l.; 21 May 1986; A. Freidberg leg.; SMNHTAU 366406 ● 1♀; Har Hermon; 1600 m a.s.l.; 29 May 2000; I. Yarom leg.; SMNHTAU ● 1♀; ibid.; 1700 m a.s.l.; 26 Jun. 1997; L. Friedman leg.; SMNHTAU 366407 ● 7♀; ibid.; 33.2994° N 35.7675° E; 1645 m a.s.l.; 16 Apr. 2021; G. Pisanty leg.; SMNHTAU 361187, 361188, 361190, 361191, 361193, 361196, 361200 ● 1♀; ibid.;
Andrena convexifrons
Wood, 2021: 26, ♀♂ [Jordan:
Endemic to the southern Levant, in scrublands and semi-arid habitats (northern Israel, Jordan;
Mid-March to early June.
One female collected from Apiaceae (Ferula).
HOLOTYPE: JORDAN ● ♀; NW, 16 km WWN of Ajlun; 600 m a.s.l.; 21 May 2007; Z. Kejval leg.;
Andrena enslinella
Stöckhert, 1924: 169–171, ♀ [S Germany:
Andrena chimaera
Blüthgen, 1949: 81 [N Germany:
Andrena enslinella Stöckhert: Stöckhert 1942: 573 (first description of ♂).
Broadly west and central Palaearctic (Gusenleitner & Schwarz 2002). Newly reported from the Levant* (Jordan*, Lebanon*).
Late April to mid-May, in Europe until June.
Presumably broadly oligolectic on Brassicaceae (Brassica, Capsella, Cardaria, Crambe, Erucastrum, Isatis, Sinapis, Sisymbrium). Also visits Asteraceae, Euphorbiaceae, Fabaceae, Plantaginaceae and Rosaceae (
The two Lebanese specimens show a 2.5% difference in COI barcodes compared to Central European populations. Morphologically, there are some slight differences. In the female sex, the Lebanese specimens show the scutum between the punctures with fine granular microreticulation, the surface dull, whereas European specimens (e.g. from Bulgaria) have the scutum polished and shining between the punctures. Specimens from Turkey are intermediate, with the scutum broadly shining but with fine shagreen. The tergal discs of Lebanese females are also slightly more finely punctate (Fig.
JORDAN ● 1♀; west, Jordan Valley, Dayr Alla [Dayr ‘Allah]; 27 Apr. 1996; Ma. Halada leg.;
Named after the Israeli coleopterist Ariel Leib Leonid (a.k.a. Laibale) Friedman, who collected most of the type series, as well as many other rare and unusual Hymenoptera.
Andrena friedmani is distinguished from other Levantine Micrandrena by the combination of small body size, finely transversely striated clypeus in the female (Figs
Female. Body length: 5.5–6 mm. — Integumental colour: Body black. Flagellum dark brown, slightly tinted reddish. Legs brown to black. Wings slightly infuscate, veins golden to brown, stigma golden centrally (Fig.
Endemic to scrublands in the southwestern Levant (northern Israel, West Bank).
February to early March.
None.
HOLOTYPE: ISRAEL ● 1♀; Hare Gilboa’ [Mount Gilboa], Har Ahino’am; 32.502° N 35.414° E; 450 m a.s.l.; 23 Feb. 2012; L. Friedman leg.; SMNHTAU 118591. – PARATYPES: ISRAEL ● 1♀; Har Ahino’am; 32.502–6° N 35.408–14° E; 440 m a.s.l.; 3 Mar. 2025; G. Pisanty leg.; SMNHTAU 463992 ● 1♂; ibid.; 32.5035° N 35.413° E; 438 m a.s.l.; pan trap; SMNHTAU 463903 ● 1♀; Hare Gilboa’, Har Ahino’am; 32.502° N 35.414° E; 450 m a.s.l.; 23 Feb. 2012; L. Friedman leg.; SMNHTAU 118600 ● 2♂; ibid.; SMNHTAU 118594, 118606. – WEST BANK: ● 1♂; Har Kabbir; 750 m a.s.l.; 5 Feb. 2015; L. Friedman leg.;
Nominative feminine singular form of the Latin adjective “hebraicus” (= Hebrew).
Within the Andrena minutula species group, A. hebraica belongs to the species around A. spreta Pérez, which are characterized in the female by a clypeus which is non-rugose, weakly domed and partly to fully shagreened, a scutum which is shagreened to partly smooth, with fine, relatively sparse punctures, and terga which are mostly shagreened and impunctate. In the Levant and Cyprus, these include A. aphroditae sp. nov., A. minutuloides, A. spreta, A. tiaretta and A. tkalcui. Andrena hebraica differs from all the above species by the sculpturing of tergal disc 3 and to a lesser extent 2, which are apically shiny, instead of completely shagreened and matt. This difference is difficult to illustrate by photographs, but is clearly visible to the eye under magnification. In addition, the clypeus is more clearly domed and more strongly and extensively shagreened compared to A. spreta and A. tiaretta (Figs
Within the Levantine and Cypriot members of the A. minutula species group, the male of A. hebraica is characterized by a flagellomere 1 which is subequal to slightly longer than 3, clypeus and scutum which are partly to fully shagreened and densely punctured, tergal discs 2 and 3 which are more strongly shagreened basally vs. apically, and characteristic genitalia lacking dorsal gonoxocite lobes and with gonostyli that converge apically. The genitalia are almost identical to those of A. povolnyi Warncke stat. nov. from Afghanistan, but they clearly differ from other similar species in the region of study as follows: lack of dorsal gonocoxite lobes (present in A. cervina and A. spreta), gonostyli more strongly converging apically compared to A. spreta and A. aphroditae, gonostyli slenderer compared to A. aphroditae, gonostyli shorter and penis valves shorter and narrower compared to A. tiaretta (Figs
Female. Body length: 5.5–6.5 mm. — Integumental colour: Body and legs predominantly black. Flagellum black, partly covered by grayish setae, distal flagellomeres occasionally brownish. Apical tarsomeres brown to black. Wings weakly infuscate, veins brown, stigma brownish centrally (Fig.
Mediterranean shrublands in Israel, the West Bank, Jordan and Lebanon. Mostly absent from the coastal plain, where it is replaced by A. tiaretta.
Late January to mid-May.
Collected mostly on Brassicaceae (Hirschfeldia, Isatis, Ochtodium, Rapistrum, Sinapis), also on Apiaceae (Ferula), Asteraceae (Anthemis, Leontodon), Campanulaceae (Campanula), Fabaceae (Trifolium) and Lamiaceae (Nepeta, Salvia).
HOLOTYPE: ISRAEL ● 1♀; Nahal Keziv [Nahal Kziv]; 33.0465° N 35.226° E; [197 m a.s.l.]; 26 Feb. 2021; G. Pisanty leg.; BOLD accession no. ANDIL490-25; SMNHTAU 357574. – PARATYPES: ISRAEL ● 2♂; Ahu Binyamina Nature Reserve; 32°30’ N 34°56’ E; 8 Mar. 2017; A. Freidberg leg.; SMNHTAU 269485, 269486 ● 1♀; Avivim; 25 Apr. 1983; A. Hefetz leg.; SMNHTAU 353608 ● 3♀; Banias; 18 Apr. 1992; R. Kasher leg.; SMNHTAU 353683 to 353685 ● 1♀; Bar’am; 4 Apr. 2014; O. Winberger leg.; SMNHTAU 183658 ● 1♀; Basmat Tab’un; 14 Apr. 1999; L. Friedman leg.; SMNHTAU 367678 ● 1♀; Beit Govrin; 15 Apr. 2017; T. Roth leg.; SMNHTAU 272634 ● 1♀; ibid.; 20 Apr. 2017; SMNHTAU 272874 ● 1♂; Beit Nir; 11 Mar. 2018; T. Roth leg.; SMNHTAU 290320 ● 1♀; ibid.; on Apiaceae;
From the Latin name for Mount Lebanon, “Libanus”, with the feminine suffix -ica, thus “libanica” meaning “of Mount Lebanon”, given the observed geographic distribution of the species.
Andrena libanica is a typical member of the A. minutula species group with the propodeal triangle entirely rugose (Fig.
As in the females, the males can be recognised as close to A. alshaykh and A. lindbergella due to the clearly punctate terga combined with the clypeus smooth and strongly punctured in the apical ½ (Figs
Female. Body length: 6–7 mm. — Integumental colour: Body black. Flagellomeres 3–10 ventrally slightly lightened by presence of greyish scales. Legs black, apical tarsomeres slightly lightened orange-brown. Wings hyaline, stigma dark brown, venation dark orange (Fig.
Andrena libanica is known from remnant cedar forest habitats in the central part of the Mount Lebanon mountain chain. It has been collected between 1726–1885 m above sea level, making it a high altitude species. Previously reported from Lebanon as A. rugulosa (
Collected in mid-May; presumably extending also into June.
Collected from Brassicaceae (Alyssum, Thlaspi).
HOLOTYPE: LEBANON ● 1♀; Mount Lebanon, Chouf Biosphere Reserve, Barouk trails; 33.6858° N 35.6986° E; 1772 m a.s.l.; 16 May 2019; Sample 1579; BOLD accession number WPATW973-22;
Andrena lindbergella
Pittioni, 1950: 42, ♀ [Cyprus:
Within the Andrena minutula species group, A. lindbergella belongs to the species around A. rugulosa Stöckhert, characterized by a smooth clypeus and punctate terga, which include also A. alshaykh Pisanty sp. nov. and A. libanica Wood sp. nov. The male is easily differentiated from A. alshaykh by the genital capsule, in which the gonostyli are uniformly curving (suddenly converging medially, producing distinct kinks in the inner and outer margins in A. alshaykh), and the penis valves are narrower (Fig.
Body length
: 6.5 mm. — Integumental colour: Body and legs black. Flagellum fully black, overlayed with minute grey setae. Wings weakly infuscate, veins and stigma dark brown (Fig.
Endemic to shrubland and sub-alpine habitats of the Troodos range in Cyprus, usually above 1200 m. Previous reports from the Levant (
Late March to mid-June.
Collected from Brassicaceae (Alyssum) and Caryophyllaceae (Arenaria).
HOLOTYPE: CYPRUS ● ♀; Troodos, Chionistra [Mount Olympus]; 17 Jun. 1939; H. Lindberg leg.;
Andrena lunaris
Pisanty & Wood, 2022:
Endemic to Mediterranean shrublands throughout the Levant (Israel, West Bank, Jordan, Lebanon*, Syria).
Early February to mid-April.
Collected on Amaryllidaceae (Allium), Asparagaceae (Ornithogalum), Asteraceae (Glebionis), Brassicaceae (Diplotaxis, Sinapis) and Orchidaceae (Cephalanthera).
HOLOTYPE: ISRAEL ● ♀; Montfort, Nahal Keziv [Montfort Castle, Nahal Kziv]; 28 Feb. 2018; G. Pisanty leg.; SMNHTAU 286280. – PARATYPES: ISRAEL ● 1♀; Bar’am; 4 Apr. 2014; N. Atkin leg.; on Sinapis; SMNHTAU ● 1♀; ibid.; O. Winberger leg.; on Glebionis ● 1♀; ibid.; pan trap ● 4♀,2♂; Bené Deror; 7 Mar. 2012; O. Afik leg.; SMNHTAU ● 1♂; Bet-Oren; 16 Feb. 1990; R. Kasher leg.; SMNHTAU ● 3♂; Bet Qeshet, 1.5 km NW; 32.74° N 35.38° E; 20 Feb. 2019; G. Pisanty leg.; SMNHTAU ● 1♂; Buraiqa NatReserve; 32.5413° N 34.979° E; 15 Feb. 2021; G. Pisanty leg.; SMNHTAU ● 1♀; Dishon; 7 Apr. 2016; O. Winberger leg.; pan trap; SMNHTAU ● 1♀; Goren; 33°02’47.7” N 35°13’19.8” E; 25 Mar. 2021; T. Novoselsky leg.; SMNHTAU ● 1♀; Haifa; 26 Feb. 1977; A. Freidberg leg.; SMNHTAU ● 1♂; Haifa; 20 Mar. 1979; A. Dafni leg.; on Cephalanthera [longifolia]; SMNHTAU ● 1♀; Hanita; 27 Mar. 1976; D. Gerling leg.; SMNHTAU ● 1♂; Har Karmila; 31°47.7’ N 35°00.9’ E; 340 m a.s.l.; 27 Mar. 2011; A. Freidberg leg.; SMNHTAU ● 1♂; Har Meron; 1000 m a.s.l.; 1 Apr. 2012; A. Freidberg leg.; SMNHTAU ● 1♀; ibid.; 1100 m a.s.l.; 17 Apr. 2000 ● 1♀; Har Meron; 32.9945° N 35.415° E; 5 Apr. 2016; G. Pisanty leg.; SMNHTAU ● 1♀,2♂; ibid.; 33.000° N 35.3927° E; 4 Apr. 2017; pan trap ● 1♀; Har Tayyasim; 31°46.3’ N 35°05.1’ E; 740 m a.s.l.; 27 Mar. 2011; A. Freidberg leg.; SMNHTAU ● 1♀,1♂; Harutsim; 26 Feb. 2009; A. Dorchin leg.; SMNHTAU ● 2♀; Hasharon, Zikhron Ya’aqov, Ramas [Ramat] Hanadiv; 12 Mar. 1990; R. Leys leg.;
Andrena luscinia
Warncke, 1975a: 46–47, ♀♂ [Central Turkey:
High elevations throughout the northern Middle East. In the Levant, occurring in northern Israel, Lebanon and Syria (
Early April to mid-June.
Collected from Rosaceae (Prunus) and Sapindaceae (Acer).
IRAN ● 1♀; Ilam province, Abda Man, Dinar Gaouh [Abdanan, Dinar Kuh Protected Area]; 1830 m a.s.l.; 12 May 2016; M. Kafka leg.; BOLD accession no. ANDGP019-25;
Andrena magunta
Warncke, 1965: 67–68, ♀ [Greece:
Andrena (Micrandrena) magunta Warncke: Gusenleitner & Schwarz 2002: 453 (first description of ♂).
Grasslands and shrublands in south-eastern Europe, Turkey and the Levant (northern Israel, Jordan*, Lebanon, Syria*;
Mid-February to late May.
Collected from Asteraceae, Brassicaceae and Rosaceae (IUCN 2024).
ISRAEL ● 1♀; Biriyya Forest; 32.99–33.00° N 35.52–53° E; 19 May 2023; G. Pisanty leg.; SMNHTAU 429811 ● 1♀; Kefar Giladi S; 25 Mar. 1997; R. Kasher leg.; SMNHTAU ● 1♀; Tivon; 2 Apr. 1975; F. Kaplan leg.; SMNHTAU ● 1♂; Yehi’am; 16 Feb. 2014; L. Friedman leg.; BOLD accession no. ANDIL405-25; SMNHTAU 173841. – JORDAN ● 1♂; 20 km NW of Amman; 420 m a.s.l.; 5 May 2006; K. Deneš leg.;
Andrena minutuloides
Perkins, 1914: 114, ♀♂ [England:
Andrena parvuloides
Perkins, 1914: 114, ♀ [England:
Andrena sparsiciliata
Alfken, 1925: 165 [Germany:
Broadly West and Central Palaearctic, in diverse habitats. In the Levant, A single female was recorded from northern Lebanon, at 1600 m (
In Europe, the species flies in two generations between April–September.
Broadly polylectic. Pollen hosts include Apiaceae, Asteraceae, Brassicaceae, Lamiaceae, Rosaceae and Scrophulariaceae (
BELGIUM ● 1♀; Liège, Pont-de-Seraing, Rue des Conquerais; 50.6214° N 5.5127° E; 27 Apr. 2021; T. Wood leg.; BOLD accession no. WPATW095-21; TJWC. – LEBANON: See
Andrena paganettina
Warncke, 1965: 64, ♀ [Greece:
Andrena (Micrandrena) paganettina Warncke: Gusenleitner & Schwarz 2002: 568–569 (first description of ♂).
Mediterranean shrublands in Greece, Turkey and all countries of the Levant (Israel, West Bank, Jordan*, Lebanon*, Syria*;
Early February to early June.
Collected from Apiaceae (Daucus), Asteraceae (Glebionis), Brassicaceae (Diplotaxis), Euphorbiaceae (Euphorbia) and Rosaceae (Malus).
ISRAEL ● 3♀; Banias; 18 Apr. 1992; R. Kasher leg.; SMNHTAU 353681, 353686, 353687 ● 2♀; Banyas; 26 May 1991; K. Warncke leg.;
Nominative feminine singular form of the Latin adjective phoenicius (=Phoenician).
Within the Andrena minutula species group, the female of A. phoenicia is characterized by the combination of a labral process which is large and trapezoidal, a clypeus which is apically protuberant and strongly domed, strongly shagreened throughout and finely, sparsely punctured, a scutum which is shagreened, finely and densely punctured, and terga which are shagreened and impunctate. The male is characterized most clearly by the genitalia which possess large rounded dorsal gonocoxite lobes and gonostyli with a strong inward king near the apex. The species is most closely related to A. stolida Warncke and A. simontornyella Noskiewicz, which share similar genitalia. The female differs in the larger labral process (Figs
Female. Body length: 6–6.5 mm. — Integumental colour: Body and legs black. Flagellum dark, distal flagellomeres often with weak reddish hue anteriorly. Apical tarsomeres brown. Wings weakly infuscate, veins and stigma brown (Fig.
Mesic habitats in Israel and Syria, likely also Lebanon.
Early April to late May.
Collected on Brassicaceae (Peltaria, Sinapis), Euphorbiaceae (Euphorbia) and Rosaceae (Crataegus).
HOLOTYPE: ISRAEL ● 1♀; Har Meron [Mount Meron]; 32.999° N 35.395° E; [1012 m a.s.l.]; 5 Apr. 2016; G. Pisanty leg.; SMNHTAU 239370. – PARATYPES: ISRAEL ● 1♀; Abirim, 24 km NE Akko; 17 Apr. 1990; R. Kasher leg.; SMNHTAU 353635 ● 1♂; Bar’am; 4 Apr. 2014; N. Atkin leg.; SMNHTAU 183543 ● 1♂; ibid.; 7 Apr. 2015; O. Winberger leg.; SMNHTAU 184627 ● 1♂; ibid.; 1 Apr. 2016; SMNHTAU 251882 ● 1♀; ibid.; 20 Apr. 2014; on Sinapis; SMNHTAU 183353 ● 1♀; Dovev; 3 Apr. 2016; O. Winberger leg.; SMNHTAU 252147 ● 2♀; Har Hermon; 33°18’ N 35°46’ E; 1700 m a.s.l.; 24 May 2012; L. Friedman leg.; BOLD accession no. ANDIL402-25; SMNHTAU 126599 ● 1♂; Har Hermon; 33.300° N 35.767° E; 1620 m a.s.l.; 11 May 2020; G. Pisanty leg;
Andrena rugothorace
Warncke, 1965: 65, ♀♂ [Greece:
Shrubland habitats in the north-east Mediterranean. In the Levant, limited to northern Israel, Lebanon and Syria* (
Late March to late May.
Broadly oligolectic on Asteraceae, subfamily Asteroideae (e.g. Anthemis) (TJW, unpublished results).
GREECE ● 1♀; Eastern Macedonia and Thrace, Abdera, immediately south of Mandra; 40.9917° N 24.9923° E; 21 May 2023; T. Wood leg.; BOLD accession no. WPATW1297-23; TJWC ● 1♀; Eastern Macedonia and Thrace, Kavala, 1 km N Ag. Andreas; 40.8811° N 24.2898° E; 23 May 2023; T. Wood leg.; BOLD accession no. WPATW1298-23; TJWC ● 1♀; Eastern Macedonia and Thrace, Kavala, Sidirochori, 1 km NW; 40.8482° N 24.1389° E; 27 May 2023; T. Wood leg.; BOLD accession no. WPATW1296-23; TJWC. – ISRAEL ● 2♂; Hanita; 27 Mar. 1976; D. Gerling leg.; SMNHTAU 353468, 354494 ● 2♂; Har Hermon; 33.2994° N 35.7675° E; 1645 m a.s.l.; 16 Apr. 2021; G. Pisanty leg.; SMNHTAU 361231, 361400 ● 1♂; ibid.; BOLD accession no. ANDIL366-22; SMNHTAU 361408 ● 5♀; ibid.; 33.3015° N 35.7737° E; 1790 m a.s.l.; 15 May 2016; SMNHTAU 242117 to 242121 ● 1♀; ibid.; BOLD accession no. ANDIL246-22; SMNHTAU 242116 ● 1♂; ibid.; 33.2855° N 35.763° E; 1420 m a.s.l.; 7 Apr. 2021; pan trap; SMNHTAU 360681 ● 2♀; ibid.; 33.2984° N 35.7683° E; 1659 m a.s.l.; 19 May 2022; SMNHTAU 392660, 392661 ● 2♂; ibid.; 33.2992° N 35.7670° E; 1644 m a.s.l.; 16 Apr. 2022; SMNHTAU 390135, 390217 ● 1♂; ibid.; 33.300° N 35.767° E; 1610 m a.s.l.; 7 Apr. 2021; SMNHTAU 360764 ● 1♀; ibid.; 33.3005° N 35.767° E; 1600 m a.s.l.; 15 May 2016; SMNHTAU 242039 ● 4♀; ibid.; 33.298–9° N 35.767–70° E; 1640–1675 m a.s.l.; 19 May 2022; sweep; SMNHTAU 392809, 392814, 392816, 392818 ● 1♂; ibid.; 33.299° N 35.769° E; 1650 m a.s.l.; 7 Apr. 2021; sweep; SMNHTAU 360390 ● 3♀; Har Meron; 32.9949° N 35.4166° E; 21 Apr. 2017; G. Pisanty leg.; SMNHTAU 270979, 270982, 270984 ● 1♀; ibid.; 33.00° N 35.395° E; 15 May 2015; SMNHTAU 213893 ● 3♀; ibid.; 33.000° N 35.3925° E; 22 Apr. 2016; SMNHTAU 240975, 240985, 240988 ● 1♂; ibid.; 32°59.7’ N 35°24.7’ E; 1000 m a.s.l.; 14 Apr. 2011; L. Friedman leg.; SMNHTAU 92591 ● 1♂; Har Meron Reserve, Gat ‘En Zeved; 32°59’ N 35°26’ E; 24 Apr. 2002; L. Friedman leg.; SMNHTAU 353519 ● 1♀; Merom Golan; 3 Apr. 1997; R. Kasher leg.; SMNHTAU 353544 ● 1♂; ibid.; SMNHTAU 353545 ● 1♀; Merom Golan, N Golan Height; 3 Apr. 1997; R. Kasher leg.; SMNHTAU 353753 ● 1♂; ibid.; SMNHTAU 353546 ● 1♀; ibid.; 20 Apr. 1997; SMNHTAU 353775 ● 3♀; Mt. Hermon; 1500 m a.s.l.; 22 May 1990; R. Kasher leg.; SMNHTAU 353660, 353671, 353672 ● 1♀; Mt. Hermon, V.[adi] Ar’ar; 1500 m a.s.l.; 22 May 1990; R. Kasher leg.; SMNHTAU 353633 ● 13♂; Mt. Meron; 900 m a.s.l.; 11 Apr. 1999; S.P.M. Roberts leg.; SPMR ● 1♂; ibid.; 14 Apr. 1999 ● 1♀; 17 km E Qiryat Shemona, Golan, 2 km SE Zomet; 16 May 1996; C. Schmid-Egger leg.; CSE ● 5♀; Ziv’on, 1kmSW; 33.02° N 35.41° E; 22 Apr. 2016; G. Pisanty leg.; SMNHTAU 240827, 240832, 240833, 240835, 240838 ● 1♀; ibid.; BOLD accession no. ANDIL242-22; SMNHTAU 240826. – LEBANON ● 2♀,2♂; Balbek-Hermel, Sefri, Haouch Snaid, AUB farm; 33.9244° N 36.0754° E; 1000 m a.s.l.; 6 Apr. 2023; T. Wood leg.; TJWC ● 1♂; ibid.; BOLD accession no. WPATW1059-23 ● 1♀; sudl. Jairoun [Tallet Ain et Tiffaha]; 23 May 2012; M. Kasparek leg.;
Andrena sillata
Warncke, 1975a: 53–54, ♀♂ [S Turkey:
Andrena sillata ssp. histrionica
Warncke, 1975a: 54, ♀♂ [Central Turkey:
As currently understood in a narrow sense (not considering ssp. histrionica), limited to shrublands and montane habitats in all countries of the Levant, as well as south-western Turkey and the island of Rhodes (
Early March to late May.
Collected from flowering trees of the families Rosaceae (Prunus, Pyrus) and Sapindaceae (Acer).
HOLOTYPE: TURKEY ● ♀; Akseki/Taurus; 1300 m a.s.l.; 25 Apr. 1973; K. Warncke leg.;
Andrena spreta
Pérez, 1895: 43–44, ♀ [Algeria:
?Andrena lampronota Pérez, 1911: 41 [Syria: ?
Andrena spreta ssp. scirpacea
Warncke, 1975a: 52, ♀♂ [SE Turkey:
Andrena (Micrandrena) spreta Pérez: Gusenleitner & Schwarz 2002: 714–715 (first description of nominate ♂).
Circum-Mediterranean (excluding the Balkan Peninsula), including all the Levant and Cyprus, in coastal, shrubland and semi-desert habitats.
Early January to late May.
Polylectic with a strong preference for Brassicaceae; minor pollen hosts include Asteraceae, Euphorbiaceae and Fabaceae (
Andrena spreta is widespread throughout most of the Mediterranean Basin. Due to the lack of strongly diagnostic characters, as well as considerable intraspecific variation, it is difficult to reliably diagnose, especially in the female. Examination of material from Israel and Cyprus shows that the species has been regularly confused with A. aphroditae sp. nov., A. hebraica sp. nov., A. tiaretta and A. tkalcui. In the Western Mediterranean it has also been regularly confused with A. curtula Pérez, A. pauxilla Stöckhert and A. pusilla Pérez (
CYPRUS ● 1♀; Káto Polemídia, 1km W Karmiotissa; 34.7118° N 32.9661° E; 197 m a.s.l.; 18 Apr. 2024; R. Santerre leg.; on the ground; BOLD accession no. RSCMC034-25; UMONS ● 1♀; Lánia; 34.8226° N 32.9132° E; 512 m a.s.l.; 7 Mar. 2024; R. Santerre leg.; flying; BOLD accession no. RSCMC033-25; UMONS ● 1♀; Lófou, 0.5km W from village; 34.8158° N 32.8684° E; 793 m a.s.l.; 27 Apr. 2024; R. Santerre leg.; at nesting site; BOLD accession no. RSCMC036-25; UMONS ● 5♀; Paphos [District], Neo Chorio; 35.021–5° N 32.354–60° E; 11 Apr. 2025; G. Pisanty leg.; on Sinapis; SMNHTAU 467247 to 467251 ● 1♂; Pissouri; 34.662–6° N 32.687–98° E; 250 m a.s.l.; 14 Apr. 2023; G. Pisanty leg.; BOLD accession no. ANDCY034-24; SMNHTAU 427242 ● 1♂; ibid.; on Asteraceae; SMNHTAU 427178 ● 2♀; ibid.; on Brassicaceae; SMNHTAU 427172, 427176 ● 1♀; ibid.; BOLD accession no. ANDCY027-24; SMNHTAU 427173 ● 1♀; ibid.; BOLD accession no. ANDCY028-24; SMNHTAU 427174 ● 1♂; Skorinou [Skarinou], Rt. E105; 34°49.5’ N 33°21.7’ E; 7 Apr. 2008; A. Freidberg leg.; SMNHTAU 438670 ● 1♀; Trimithousa, Evretou dam; 34.9738° N 32.4777° E; 179 m a.s.l.; 22 Apr. 2024; R. Santerre leg.; on Apiaceae; BOLD accession no. RSCMC035-25; UMONS. – ISRAEL ● 1♀; B.S.Hazeva [Hazeva Field School]; 10 Jan. 1998; S. Alfi leg.; SMNHTAU 367679 ● 6♀; Be’er Sheva, Negev Monument; 31.2665° N 34.8215° E; 350 m a.s.l.; 18 Feb. 2025; G. Pisanty leg.; SMNHTAU 463068, 463079 to 463083 ● 15♀,2♂; Beersheba; 15 Apr. 1970; H. Bytinski-Salz leg.; SMNHTAU ● 2♀; ibid.; 28 Mar. 19[??] ● 1♂; Beit Haarava; 23 Mar. 1946; SMNHTAU ● 1♀; Beit Nir; 11 Mar. 2018; T. Roth leg.; on Biscutella didyma; SMNHTAU 290292 ● 1♀; Ben Shemen Forest; 31.93° N 34.972° E; 18 Feb. 2017; G. Pisanty leg.; SMNHTAU 268569 ● 1♀; Bet Guvrin; 31.610–6° N 34.890° E; 17 Feb. 2023; G. Pisanty leg.; sweep; SMNHTAU 420842 ● 1♀; Bet Guvrin; 31.611° N 34.890° E; 17 Feb. 2023; G. Pisanty leg.; pan trap; SMNHTAU 420827 ● 2♂; Bet Ha’Emeq; 6 Feb. 2000; L. Friedman leg.; SMNHTAU ● 1♀; Bet Nir, 1.5km SSE; 31.6347° N 34.879° E; 17 Feb. 2023; G. Pisanty leg.; pan trap; SMNHTAU 420906 ● 2♀; Bet Shiqma; 31.643° N 34.619° E; 1 May 2023; E.L.A.E. leg.; pan trap; SMNHTAU 462759, 462761 ● 1♂; Brurchajl [Bror Hayil]; 15 Feb. 1960; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; Buraiqa NatReserve; 32.5413° N 34.979° E; 15 Feb. 2021; G. Pisanty leg.; SMNHTAU 356742 ● 3♀; Carmel; 12 Mar. 1940; H. Bytinski-Salz leg.; SMNHTAU ● 1♂; Dag [?]; 8 Jan. 1940; SMNHTAU ● 1♂; Deganya A, Bet Gordon; 3 Mar. 1942; Y. Palmoni leg.; on Sinapis alba & Diplotaxis; SMNHTAU 181509 ● 1♀; EinGedi; 14 Apr. 1962; Kugler leg.; SMNHTAU 353589 ● 1♀; En Kerem; 28 Mar. 1969; Y. Ayal. leg.; SMNHTAU 353590 ● 1♀; Geulim; 18 Mar. 2015; I. Eliakim leg.; SMNHTAU 185815 ● 1♀; Gilat Research Center, 500 m NNE; 31.341° N 34.6693° E; 2 Mar. 2022; G. Pisanty leg.; pan trap; SMNHTAU 386286 ● 1♂; Gilat Research Center, 500 m NNE, fallow field; 31.3405° N 34.670° E; 2 Mar. 2022; G. Pisanty leg.; sweep; SMNHTAU 385041 ● 1♀; Gilat Research Center, fallow field; 31.3372° N 34.663° E; 2 Mar. 2022; G. Pisanty leg.; sweeping; SMNHTAU 385003 ● 1♂; Golan, Gilbon; 21 Apr. 1988; I. Yarom leg.; SMNHTAU 353505 ● 1♀; Gvar’am NR; 31.58° N 34.59° E; 1 Mar. 2023; G. Pisanty leg.; sweep; SMNHTAU 422747 ● 1♂; Gvulot; 22 Feb. [19]84; E. Shney-Dor leg.; SMNHTAU 353457 ● 4♀, 2♂; Haifa Carmel; 17 Feb. 1973; A. Freidberg leg.; SMNHTAU ● 1♀; Haniel; 23 Apr. 2023; S. Asis leg.; SMNHTAU 414782 ● 1♀; Har Hermon; 33.2992° N 35.7670° E; 1644 m a.s.l.; 16 Apr. 2022; G. Pisanty leg.; pan trap; SMNHTAU 390173 ● 1♂; Har Meron; 800 m a.s.l.; 5 Mar. 2011; A. Freidberg leg.; SMNHTAU 89132 ● 1♀; ibid.; 1100 m a.s.l.; 17 Apr. 2000; SMNHTAU 353670 ● 1♀; Har’el; 13 Apr. 2009; G. Pisanty leg.; on Sinapis arvensis; SMNHTAU 27696 ● 1♀; Har’el; 21 Feb. 2020; K. Levy leg.; SMNHTAU 338152 ● 1♀; Hazeva; 21 Feb. 2008; A. Gotlieb leg.; SMNHTAU 22120 ● 1♀; Herzliya; 21 Apr. 1966; H. Bytinski-Salz leg.; SMNHTAU ● 3♀; Herzliyya; 7 May 1982; A. Freidberg leg.; Malaise trap; SMNHTAU 353696 to 353698 ● 1♀; ibid.; 9 May 1982; SMNHTAU 354478 ● 1♀; ibid.; 12 May 1982; SMNHTAU ● 1♂; Herzliyya; 18 Dec. 2000; A. Freidberg & L. Friedman leg.; SMNHTAU 353517 ● 2♂; Hof Rosh Haniqra N.R.; 33.076–85° N 35.105–9° E; 18 Mar. 2025; G. Pisanty leg.; SMNHTAU 464966, 464968 ● 1♀; Hof Rotem Shezaf, 3kmS’EnGev; 32°46’ N 35°38.3’ E; –200 m a.s.l.; 21 Mar. 2010; M. Guershon leg.; SMNHTAU 53178 ● 1♂; Holon; 27 Feb. 1973; H. Bytinski-Salz leg.; SMNHTAU ● 1♂; ibid.; 12 Mar. 1973; ● 2♂; ibid.; 8 Mar. 1975; SMNHTAU 353465, 353466 ● 1♀; Holot Shunera; 30.941° N 34.597° E; 17 Mar. 2017; G. Pisanty leg.; pan trap; SMNHTAU 269103 ● 1♀; Horeshim; 32.138° N 34.976° E; 11 Feb. 2017; G. Pisanty leg.; SMNHTAU 268534 ● 1♀; Hulda; 23 Mar. 2017; T. Roth; SMNHTAU 272645 ● 1♀; Jerusalem; 15 Mar. 1940; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; ibid.; 1 Mar. 1964 ● 1♂; Jerusalem, Mt.Scopus; 15 Mar. 1946; SMNHTAU ● 1♀; Kefar Barukh; 32.650° N 35.175–180° E; 2 May 2023; E.L.A.E. leg.; pan trap; SMNHTAU 462994 ● 1♀; Kefar Giladi N; 25 Mar. 1997; R. Kasher leg.; SMNHTAU 353758 ● 1♂; Kefar Menahem; 10 May 2009; G. Pisanty leg.; BOLD accession no. ANDIL452-25; SMNHTAU 28655 ● 1♀; Kefar Uriyya–Tarum; 31.78–80° N 34.95–97° E; 25 Feb. 2017; G. Pisanty leg.; SMNHTAU 268529 ● 1♀; Kfar Giladi; 18 May 1958; H. Bytinski-Salz leg.; SMNHTAU ● 2♀; Kfar Masaryk; 32.87° N 35.13° E; 4 Apr. 2023; E.L.A.E. leg.; pan trap; SMNHTAU 462833, 462851 ● 1♀; Kfar Menachen; 8 Mar. 2008; U. Roll leg.; SMNHTAU 25012 ● 1♂; Kineret; 4 Mar. 1968; H. Bytinski-Salz leg.; SMNHTAU ● 1♂; Kinneret (Qevuza); 12 Apr. 1942; Y. Palmoni leg.; SMNHTAU 181499 ● 1♀; ibid.; 8 Apr. 1936; on thistles; SMNHTAU 181512 ● 1♂; Klahim; 31.453° N 34.691° E; 12 Mar. – 30 Apr. 2023; E.L.A.E. leg.; pan trap; SMNHTAU 462963 ● 1♀; Lachish; 18 Feb. 2020; T. Roth; on Isatis lusitanica; SMNHTAU 338257 ● 1♀; Lahav; 5 Jan. 1971; Kugler leg.; SMNHTAU 353585 ● 1♂; Lahav; 27 Feb. 1974; A. Freidberg leg.; SMNHTAU ● 1♀; Lakhish; 18 Feb. 2013; T. Shapira leg.; BOLD accession no. ANDIL153-22; SMNHTAU 133175 ● 1♀; Lakhish, 2km E; 31.556° N 34.87° E; 5 Feb. 2016; G. Pisanty leg.; SMNHTAU 233249 ● 1♀; ibid.; pan trap; SMNHTAU 233261 ● 1♀; Lakhish, 3km NE; 31.575° N 34.870° E; 11 Mar. 2016; G. Pisanty leg.; SMNHTAU 236051 ● 1♂; ibid.; 31.578° N 34.870° E; 19 Feb. 2016; SMNHTAU 234225 ● 1♂; ibid.; 26 Feb. 2016; BOLD accession no. ANDIL219-22; SMNHTAU 234628 ● 2♀; ibid.; 31.579° N 34.871° E; 4 Mar. 2016; on Sinapis; SMNHTAU 235193, 235194 ● 1♀; ibid.; BOLD accession no. ANDIL224-22; SMNHTAU 235192 ● 5♀; Lehavim; 31.365° N 34.830° E; 28 Jan. 2015; G. Pisanty leg.; pan trap; SMNHTAU 202230 to 202232, 202236, 202281 ● 5♀; Mashabe Sade; 16 Feb. 1976; A. Freidberg leg.; SMNHTAU 353653 to 353657 ● 1♀; Mashabei Sade; 16 Feb. 1976; M. Kaplan leg.; SMNHTAU 353652 ● 1♀; Masmiya; 27 Feb. 1957; on Vicia faba; SMNHTAU ● 1♀; Ma’yan Barukh; 33.232° N 35.611° E; 29 Mar. 2023; E.L.A.E. leg.; pan trap; SMNHTAU 462805 ● 1♂; ibid.; 3 May 2023; SMNHTAU 462787 ● 3♀; Me’arat Yishah, 0.5km E; 32.718° N 35.007° E; 22 Feb. 2019; G. Pisanty leg.; SMNHTAU 321608, 321612, 321694 ● 1♀; ibid.; BOLD accession no. ANDIL313-22; SMNHTAU 321613 ● 1♂; ibid.; BOLD accession no. ANDIL315-22; SMNHTAU 321644 ● 1♀; Mishmar Hanegev; 24 Apr. 2023; S. Asis leg.; SMNHTAU 414772 ● 2♀; Monfort; 4 Mar. 1976; M. Kaplan leg.; SMNHTAU 353623, 353625 ● 1♂; ibid.; SMNHTAU 354493 ● 1♀; ibid.; A. Freidberg leg.; SMNHTAU 353624 ● 1♂; Montfort; 10 Mar. 1981; A. Freidberg leg.; SMNHTAU 353537 ● 4♀; ibid.; F. Kaplan leg.; SMNHTAU 354471 to 354474 ● 2♂; ibid.; SMNHTAU 353538, 353543 ● 2♂; Montfort, Nahal Keziv; 28 Feb. 2018; G. Pisanty leg.; SMNHTAU 286317, 286322 ● 1♂; ibid.; BOLD accession no. ANDIL281-22; SMNHTAU 286323 ● 1♀; N.[ahal] Amud; 23 Feb. 1983; I. Yarom leg.; SMNHTAU 353659 ● 1♂; N.[ahal] Oren; 4 Mar. 1975; M. Kaplan leg.; SMNHTAU 353478 ● 1♀; Nachshon; 20 Feb. 2020; K. Levy leg.; SMNHTAU 338535 ● 1♀; Nachson; 20 Feb. 2020; T. Roth leg.; SMNHTAU 346690 ● 1♀; Nahal Alexander; 5 Apr. 2016; K. Levy leg.; SMNHTAU 250395 ● 1♀; ibid.; 24 Apr. 2016; SMNHTAU 250665 ● 1♀; ibid.; 23 Mar. 2017; SMNHTAU 274012 ● 1♀; ibid.; 8 Mar. 2018; SMNHTAU 291800 ● 1♀; ibid.; 5 Apr. 2018; SMNHTAU 291547 ● 1♀; ibid.; 6 Apr. 2018; SMNHTAU 291483 ● 1♀; ibid.; 19 Mar. 2019; SMNHTAU 311270 ● 1♀; ibid.; 27 Feb. 2020; SMNHTAU 337968 ● 1♀; ibid.; 29 Feb. 2020; SMNHTAU 337455 ● 1♀; ibid.; 11 Mar. 2019; on Senecio joppensis; SMNHTAU 311506 ● 1♀; ibid.; 18 Mar. 2019; on Brassica tournefortii; SMNHTAU 311529 ● 1♀; ibid.; 2 Apr. 2020; on Euphorbia terracina; SMNHTAU 337461 ● 1♀; ibid.; 3 Apr. 2020; SMNHTAU 337473 ● 4♀; Nahal Hazav, BitronotRuhama; 31°32’ N 34°42’ E; 5 Apr. 2005; A. Freidberg leg.; SMNHTAU 353703, 354475 to 354477 ● 4♀; Nahal Keziv; 33.0465° N 35.226° E; 26 Feb. 2021; G. Pisanty leg.; SMNHTAU 357575 to 357578 ● 3♂; ibid.; SMNHTAU 357654, 357656, 357660 ● 2♂; Nahal Shemarya; 31.341° N 34.6567° E; 2 Mar. 2022; G. Pisanty leg.; pan trap; SMNHTAU 386185, 386186 ● 2♂; ibid.; 31.341° N 34.6568° E; sweeping; SMNHTAU 385074, 385076 ● 1♂; Nahal Ye’elim; 21 Apr. 2005; L. Friedman leg.; SMNHTAU 354487 ● 1♀; Nahshon; 23 May 2009; G. Pisanty leg.; SMNHTAU 31453 ● 1♀; ibid.; 10 Feb. 2010; pan trap; SMNHTAU 31903 ● 1♀; Nahshonim; 27 Apr. 2023; S. Asis leg.; SMNHTAU 414777 ● 1♀; Nes Ziona, orchard; 27 Feb. 1991; W. Kuslitzky leg.; SMNHTAU 353632 ● 1♀; Netanya, Irus Ha’Argaman NR; 32.287° N 34.842° E; 24 Feb. 2021; G. Pisanty leg.; BOLD accession no. ANDIL348-22; SMNHTAU 357205 ● 1♂; Or ‘Aqiva, 1km E; 32.493° N 34.934° E; 33 m a.s.l.; 2 Mar. 2025; L. Friedman leg.; SMNHTAU 464106 ● 1♂; Park Britannia; 10 Feb. 2011; T. Koznichki leg.; pan trap; SMNHTAU 81247 ● 3♀; ibid.; 24 Apr. 2011; SMNHTAU 354427 to 354429 ● 3♀; Park Britannia; 20 Apr. 2015; T. Chaprazaro leg.; SMNHTAU 185250, 185255, 185264 ● 9♀; ibid.; 14 Apr. 2016; SMNHTAU 251132 to 251134, 251136, 251137, 251661, 251662, 251664, 251671 ● 1♀; ibid.; BOLD accession no. ANDIL434-25; SMNHTAU 251670 ● 2♀; Park Britanya; 15 Apr. 2010; T. Koznichki leg.; on Erucaria; SMNHTAU 59603, 59604 ● 2♀; ibid.; 11 Feb. 2011; pan trap; SMNHTAU 81266, 81281 ● 1♂; Park haYarden; 32°54.7’ N 35°37.6’ E; –190 m a.s.l.; 22 May 2011; M. Guershon leg.; BOLD accession no. ANDIL514-25; SMNHTAU 94347 ● 1♀; ParkHayarden; 27 Apr. 1984; A. Freidberg leg.; SMNHTAU 353706 ● 1♂; ibid.; SMNHTAU 353480 ● 1♀; Pura Nature Reserve; 31.496° N 34.778° E; 27 Mar. 2015; G. Pisanty leg.; SMNHTAU 208232 ● 1♀; Pura NR; 31°29’48” N 34°46’35” E; 200 m a.s.l.; 22 Feb. 2022; L. Friedman leg.; SMNHTAU 384828 ● 1♂; Qazrin; 32°59.2’ N 35°41.8’ E; 335 m a.s.l.; 22 May 2011; A. Freidberg leg.; BOLD accession no. ANDIL513-25; SMNHTAU 94280 ● 1♀; Qedma; 17 Feb. 2010; G. Pisanty leg.; pan trap; BOLD accession no. ANDIL312-22; SMNHTAU 31897 ● 1♂; Qiryat Gat - Bet Qama; ca. Jan. 2011; I. Van Rijn leg.; BOLD accession no. ANDIL508-25; SMNHTAU 81065 ● 1♀; R.G.n [?Ramat Gan]; 3 Feb. 1940; SMNHTAU ● 1♀; Ramat haNadiv; 13 Feb. 2013; T. Shapira leg.; SMNHTAU 150961 ● 2♀; Ramleh; SMNHTAU ● 2♀; Ramot Naftali; 24 Apr. 2014; O. Winberger leg.; SMNHTAU 183286, 183437 ● 1♀; Road 87, 260m E Yehudiyya Jcn, Plot D6; 32.902° N 35.650° E; –160 m a.s.l.; 11 Apr. 2019; A. Dorchin, Y. Mersman & O. Halbershtat leg.; BOLD accession no. ANDIL455-25; SMNHTAU 307451 ● 3♀; Rosh Ha’Ayin; 6 Apr. 2015; A. Freidberg leg.; SMNHTAU 223984, 223991, 223994 ● 1♂; ibid.; SMNHTAU 224019 ● 1♀; Rosh Ha’Ayin, East, Hirbet Kseyfe; 32.091° N 34.999° E; 140 m a.s.l.; 7 Mar. 2022; L. Friedman leg.; SMNHTAU 386914 ● 1♀; Rosh Ha’ayin Forest; 32.1013° N 34.9695° E; 28 Mar. 2022; G. Pisanty leg.; sweeping; SMNHTAU 388617 ● 2♀; Sa’ad; 31.468° N 34.5287° E; 21 Jan. 2015; G. Pisanty leg.; pan trap; SMNHTAU 201960, 201961 ● 4♀; ibid.; 31.469° N 34.528° E; on Brassicaceae; SMNHTAU 201971, 201973, 201974, 201977 ● 1♀; ibid.; BOLD accession no. ANDIL176-22; SMNHTAU 201976 ● 4♂; Sederot; 27 Feb. 1974; A. Freidberg leg.; SMNHTAU ● 6♀; Sha’alvim; 7 Feb. 2010; G. Pisanty leg.; pan trap; SMNHTAU 31806, 31842, 31853 to 31855, 31875 ● 4♂; ibid.; SMNHTAU 31804, 31805, 31856, 31877 ● 1♀; Sha’alvim; 16 Mar. 2017; T. Roth leg.; BOLD accession no. ANDIL267-22; SMNHTAU 272520 ● 2♀; Snir - Hermon Field Study Center; 27 Mar. 1997; R. Kasher leg.; SMNHTAU 354440, 354442 ● 1♀; Snir, Hermon Field Study Center; 13 Mar. 1997; R. Kasher leg.; SMNHTAU 354449 ● 1♂; T. A b [?Tel Aviv]; 13 Feb. 1940; SMNHTAU ● 1♀; Tal Shahar; 2 Apr. 2010; G. Pisanty leg.; on Sinapis alba; SMNHTAU 31926 ● 1♂; Tel Aviv; 18 Mar. 1974; H. Bytinski-Salz leg.; SMNHTAU 354459 ● 1♂; Tel Aviv, 4 Lipsky St.; 32.0883° N 34.7888° E; 6 Mar. 2015; G. Pisanty leg.; BOLD accession no. ANDIL189-22; SMNHTAU 206177 ● 1♀; Tel Aviv, Tzapari, Park HaYarqon; 10 m a.s.l.; 18 Mar. 2015; T. Novoselsky & A. Freidberg leg.; on Eucalyptus camaldulensis; SMNHTAU 207446 ● 1♂; Tel Aviv BG.; 5 Mar. 1972; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; ibid.; 10 Mar. 1972 ● 1♂; ibid.; 15 Feb. 1973 ● 1♂; ibid.; 21 Feb. 1973 ● 1♂; ibid.; 8 Mar. 1974; SMNHTAU 354488 ● 1♂; Tel Aviv N; 17 Feb. 1973; H. Bytinski-Salz leg.; SMNHTAU ● 3♂; ibid.; 20 Feb. 1973 ● 1♂; Tel Aviv University; 15 Feb. 2007; W. Kuslitzky leg.; Malaise trap; SMNHTAU 354492 ● 1♂; Tel Sokho; 280 m a.s.l.; 4 Feb. 2020; L. Friedman leg.; BOLD accession no. ANDIL468-25; SMNHTAU 330928 ● 1♀; Tel Zafit; 31 Mar. 2018; T. Roth leg.; on Rapistrum rugosum; SMNHTAU 290830 ● 1♀; Tivon; 30 Mar. 19[??]; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; W.[adi] Saar Golan; 1 Jun. 1970; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; Ya’ar Kedoshim; 26 Feb. 2017; Y. Farago leg.; on Sinapis alba; SMNHTAU 272178 ● 1♀; Ya’ar Nehosha; 14 Apr. 2016; T. Chaprazaro leg.; SMNHTAU 251680 ● 1♀; ibid.; 15 Apr. 2016; BOLD accession no. ANDIL435-25; SMNHTAU 251694 ● 1♀; Ya’ar Nehusha; 15 Feb. 2011; T. Koznichki leg.; pan trap; SMNHTAU 81365 ● 1♂; ibid.; SMNHTAU 81356 ● 1♀; Yagur; 32.74° N 35.07° E; 24 Apr. 2015; G. Pisanty leg; BOLD accession no. ANDIL207-22; SMNHTAU 214114 ● 1♂; Yerushalayim; 24 Feb. 2014; A. Gotlieb leg.; SMNHTAU 184220 ● 1♂; Zemach; 21 Feb. 19[??]; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; Zemah; 32°42.3’ N 35°35.9’ E; 21 Mar. 2010; M. Guershon leg.; SMNHTAU 53149 ● 1♀; ZikhronYaakov; 9 Feb. 1988; I. Yarom leg.; SMNHTAU 353722 ● 1♂; Zomet Nappah; 3 Mar. 2016; L. Friedman leg.; BOLD accession no. ANDIL425-25; SMNHTAU 235044 ● 2♀; Zova; 10 May 2012; Y. Berner leg.; SMNHTAU 132754, 132756 ● 1♀; Zur Moshe; 16 Mar. 2015; I. Eliakim leg.; SMNHTAU 185768. – JORDAN ● 1♀; Al Maghtas; 24 Feb. 1942; H. Bytinski-Slaz leg.; SMNHTAU 353599 ● 3♀; ibid.; 25 Feb. 1942; SMNHTAU 353597, 353598, 402794 ● 3♀; 30 km NW Ajlun; 600 m a.s.l.; 29 Apr. 2006; K. Deneš leg.;
Andrena stolida
Warncke, 1975a: 51, ♀♂ [central Turkey:
Mediterranean shrublands in Turkey and the Levant* (Israel*, Jordan*, Lebanon*, Syria*).
Late February to late May.
None.
HOLOTYPE: TURKEY ● ♀; Ankara; 21 May. 1972; K. Warncke leg.;
Andrena sulfurea
Wood, 2022:
Endemic to desert habitats in central Syria.
Late March to late April.
None.
HOLOTYPE: SYRIA ● ♂; Homs, As-Shuknah [As Sukhnah], 22 km E; 250 m a.s.l.; 24 Mar. 1988; L. Blank leg.;
Andrena tiaretta
Warncke, 1974b: 12, 38, ♀♂ [Algeria:
Andrena orientalis
Kratochwil, 2015: 1412, 1418, ♀♂ [Israel:
South Mediterranean. In the Levant, limited to sandy and hamra soils along Israel’s coastal plain. Reports from Lebanon, Syria and Iran (
Late January to late April, in north Africa rarely until early June.
Collected from Brassicaceae (Sinapis).
The female of Andrena tiaretta is extremely similar to A. spreta, and the two species have been repeatedly confused (
ISRAEL ● 1♀; Bat Jam [Yam]; 31 Jan. 1941; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; Bené Deror [Bnei Dror]; 7 Mar. 2012; O. Afik leg.; SMNHTAU 106405 ● 1♂; En Sarid; 2 Apr. 2014; I. Eliakim leg.; SMNHTAU 152530 ● 3♀; ibid.; 31 Mar. 2015; SMNHTAU 185841, 185844, 185849 ● 1♀; En Vered; 3 Feb. 2015; I. Eliakim leg.; BOLD accession no. ANDIL408-25; SMNHTAU 185656 ● 18♂; Gvar’am NR; 31.58° N 34.59° E; 1 Mar. 2023; G. Pisanty; sweep, on Brassicaceae; SMNHTAU 422726 to 422732, 422734 to 422744 ● 1♀; HaKefar HaYaroq, Zomet Gelilot [Glilot Junction]; 22 Apr. 2011; A. Freidberg leg.; SMNHTAU 93016 ● 1♂; Herzliyah; 22 Mar. 1942; H. Bytinski-Salz leg.; SMNHTAU ● 1♂; ibid.; 17 Mar. 1945 ● 2♀; Herzliyya, hill; 32°11’ N 34°49’ E [more precisely 32.156° N 34.847° E]; 7 Mar. 2008; A. Freidberg leg.; SMNHTAU 354479, 354480 ● 1♂; Hof Dor–HaBonim N.R.; 32.630–44° N 34.922–8° E; 2 Mar. 2025; G. Pisanty leg.; SMNHTAU 464046 ● 2♂; ibid.; 32.638–43° N 34.922–8° E; L. Friedman leg.; SMNHTAU 464069, 464070 ● 1♀; Kefar ‘Avoda; 13 Mar. 2012; O. Afik leg.; SMNHTAU 106273 ● 1♀; ibid.; 1 Apr. 2012; SMNHTAU 106534 ● 1♂; Mavqi’im; 31°37’ N 34°34’ E; 18 Feb. 2004; L. Friedman leg.; SMNHTAU 366433 ● 1♂; ibid.; BOLD accession no. ANDIL496-25; SMNHTAU 366432 ● 1♀; Mik - Jis [Mikveh Israel]; 26 Apr. 1940; on Sinapis; SMNHTAU ● 1♂; Nahal Alexander; 10 Apr. 2019; K. Levy leg.; SMNHTAU 185035 ● 1♂; ibid.; 29 Feb. 2020; SMNHTAU 337456 ● 1♀; Nes Ziyyona; 26 Jan. 2014; G. Pisanty leg.; SMNHTAU 152463 ● 7♀; ibid.; 31.928° N 34.78° E; 13 Mar. 2015; SMNHTAU 207052 to 207055, 207057 to 207059 ● 1♀; ibid.; BOLD accession no. ANDIL418-25; SMNHTAU 207056 ● 1♂; Netanya, Irus Ha’Argaman NR; 24 Feb. 2021; ITI Bee Course leg.; SMNHTAU 366435 ● 1♂; Pardes Hanna; 8 Apr. 1946; SMNHTAU ● 1♀; Petah-Tikva; 18 Feb. 1956; I. Kugler leg.; SMNHTAU 353588 ● 1♀; Ramla; 28 Mar. 1972; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; R.G n [?Ramat Gan]; 3 Feb. 1940; SMNHTAU ● 2♂; Sde Uziyahu; 31.753° N 34.667° E; 13 Mar. 2023; E.L.A.E. leg.; pan trap; SMNHTAU 462966, 462967 ● 3♂; Sederot; 27 Feb. 1974; A. Freidberg leg.; SMNHTAU ● 1♂; Tel Aviv; 4 Mar. 1970; H. Bytinski-Salz leg.; SMNHTAU ● 1♂; ibid.; 17 Mar. 1970 ● 2♂; ibid.; 5 Mar. 1973 ● 1♂; ibid.; 10 Mar. 1972 ● 2♀; ibid.; 8 Mar. 1974 ● 2♀; Tel Aviv, Ramat Aviv; 32.130° N 24.802° E; 6 Mar. 2015; G. Pisanty leg.; SMNHTAU 206340, 206345 ● 1♀; ibid.; BOLD accession no. ANDIL415-25; SMNHTAU 206344 ● 3♂; ibid.; SMNHTAU 206295, 206303, 206325 ● 1♂; ibid.; BOLD accession no. ANDIL414-25; SMNHTAU 206331 ● 1♂; ibid.; 32.130° N 34.801° E; 1 Apr. 2017; SMNHTAU 270448 ● 2♀; ibid.; on Brassicaceae; SMNHTAU 270435, 270437 ● 3♂; ibid.; 270434, 270437, 270447 ● 1♂; Tel Aviv, Tel Barukh; 19 Mar. 1997; L. Friedman leg.; SMNHTAU 353504 ● 1♂; Tel Aviv, Tzapari, Park haYarqon; 10 m a.s.l.; 18 Mar. 2015; T. Novoselsky & A. Freidberg leg.; SMNHTAU 207449 ● 2♀,2♂; Tel Aviv BG; 4 Mar. 1970; H. Bytinski-Salz leg.; SMNHTAU ● 2♀,4♂; ibid.; 1 Mar. 1972 ● 2♀,4♂; ibid.; 10 Mar. 1972 ● 1♂; ibid.; 14 Mar. 1973 ● 1♀,2♂; ibid.; 20 Mar. 1973 ● 1♀; Tel Aviv N; 17 Feb. 1973; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; Tel Aviv University, Botanical Garden; 32°06’50” N 34°48’31” E; 2–5 Apr. 2012; SMNHTAU 121428 ● 3♀; ibid.; L. Friedman leg.; 121523, 121525, 121531 ● 1♂; ibid.; A. Golan leg.; SMNHTAU 121458 ● 1♂; Tel Aviv University, Botanical Garden; 22 Mar. 2016; L. Friedman leg.; SMNHTAU 238282 ● 1♀; Yavne; 4 Feb. 1976; A. Freidberg leg.; SMNHTAU 353645 ● 1♂; Zur Moshe; 16 Mar. 2015; I. Eliakim leg; SMNHTAU 185790 ● 1♂; ibid.; BOLD accession no. ANDIL409-25; SMNHTAU 185767. – WEST BANK ● 1♂; 10 Km East Jerusalem [likely erroneous]; 18 Mar. [19]70; H. Bytinski-Salz leg.; SMNHTAU.
Andrena testacea
Warncke, 1975a (nec Andrena gwynana var. testacea Dalla Torre 1877): 56–57, ♀♂ [West Bank:
Andrena tkalcui Gusenleitner & Schwarz, 2002: 765, nom. nov. for Andrena testacea Warncke, 1975.
Shrubland and semi-desert habitats in the northern Middle East, including all countries of the Levant (Israel, West Bank, Jordan, Lebanon*, Syria).
Late January to late May.
Collected from Apiaceae, Brassicaceae (Hirschfeldia, Sinapis) and Rosaceae (Prunus).
HOLOTYPE: WEST BANK ● 1♀; Jericho; 20–28 Apr. 1927; Dr. Enslin leg.;
Andrena tringa
Warncke, 1973: 30, ♀♂ [Turkey:
Eastern Europe, Turkey and the Levant (northern Israel and Lebanon;
Early April to Late June.
Presumably oligolectic on Brassicaceae (Alyssum, Barbarea, Brassica, Crambe, Draba, Erucastrum, Isatis, Lepidium, Peltaria, Raphanus, Sinapis, Sisymbrium). Also visits Apiaceae, Asteraceae, Crassulaceae, Liliaceae and Rosaceae (IUCN 2024 and new records).
ISRAEL ● 1♀; Har Hermon; 1400 m a.s.l.; 18 Apr. 2012; L. Friedman leg.; SMNHTAU 124821 ● 2♀; ibid.; 33°18’ N 35°46’ E; 1700 m a.s.l.; 6 Jun. 2013; SMNHTAU 142440, 142446 ● 2♀; ibid.; 33.30° N 35.77° E; 1600–1800 m a.s.l.; 17 Jun. 2020; G. Pisanty leg.; SMNHTAU 336030, 336031 ● 1♀; ibid.; 33.302° N 35.773° E; 1820 m a.s.l.; SMNHTAU 336104 ● 11♀; ibid.; 33.2994° N 35.7675° E; 1645 m a.s.l.; 16 Apr. 2021; SMNHTAU 361198, 361203, 361205, 361206, 361208, 361209, 361215, 361420, 361423, 361425, 361429 ● 16♂; ibid.; SMNHTAU 361225, 361249, 361255, 361262, 361266, 361289, 361308, 361325, 361336, 361337, 361340, 361410, 361461 to 361464 ● 1♀; ibid.; BOLD accession no. ANDIL368-22; SMNHTAU 361419 ● 1♂; ibid.; BOLD accession no. ANDIL367-22; SMNHTAU 361411 ● 1♀; ibid.; stylopized; SMNHTAU 361201 ● 7♂; ibid.; 33.299° N 35.769° E; 1650 m a.s.l.; 7 Apr. 2021; sweep; SMNHTAU 360394, 360397, 360420 to 360424 ● 12♂; ibid.; 33.2991° N 35.7667° E; 1644 m a.s.l.; 16 Apr. 2022; pan trap; SMNHTAU 390373, 390378, 390393, 390394, 390466, 390475, 390477, 390480, 390484, 390492, 390498, 390512 ● 4♀; ibid.; pan trap, stylopized; SMNHTAU 390408, 390414, 390418, 390476 ● 1♀; ibid.; 33.2992° N 35.7668° E; 1642 m a.s.l.; 19 May 2022; pan trap; SMNHTAU 392628 ● 23♂; ibid.; 33.2992° N 35.7670° E; 1644 m a.s.l.; 16 Apr. 2022; SMNHTAU 390006 to 390008, 390014, 390015, 390140, 390142, 390155, 390157, 390161, 390219, 390220, 390223 to 390227, 390229, 390231, 390233, 390234, 390236, 390237 ● 3♀; ibid.; pan trap, stylopized; SMNHTAU 390178, 390240, 390241 ● 2♂; ibid.; 33.2996° N 35.7677° E; 1642 m a.s.l.; pan trap; SMNHTAU 390591, 390594 ● 1♀; ibid.; 19 May 2022; SMNHTAU 392734 ● 1♀; ibid.; 33.300° N 35.767° E; 1600 m a.s.l.; 11 May 2020; SMNHTAU 334870 ● 6♂; ibid.; 1610 m a.s.l.; 7 Apr. 2021; SMNHTAU 360762, 360765, 360766, 360795, 360803, 360811 ● 1♀; ibid.; 33.3015° N 35.7735° E; 1790 m a.s.l.; 18 Jun. 2020; SMNHTAU 335999 ● 3♂; ibid.; 33.2992° N 35.767° E; 1644 m a.s.l.; 16 Apr. 2022; on Gagea; SMNHTAU 389984, 389985, 389987 ● 2♀; Har Hermon, Busheri turn; 1770 m a.s.l.; 1 Jun. 2016; L. Friedman leg.; SMNHTAU 247884, 247886 ● 1♀; Hermon; 1300 m a.s.l.; 27 Apr. 1978; D. Furth leg.; SMNHTAU ● 1♀; ibid.; 1700 m a.s.l.; 27 Jun. 1973; SMNHTAU 354464 ● 4♀; Hermon; 33.291–4° N 35.747–51° E; 1440–1550 m a.s.l.; 29 Apr. 2022; G. Pisanty leg.; sweep; SMNHTAU 391578 to 391581 ● 1♀; Hermon, Biq’at Man; 33.292° N 35.751° E; 1450 m a.s.l.; 29 Apr. 2022; G. Pisanty leg.; on Peltaria angustifolia; SMNHTAU 391532 ● 1♀; Hermon, Har Shezif; 33.286° N 35.7524° E; 1447 m a.s.l.; 16 Apr. 2022; G. Pisanty leg.; pan trap; SMNHTAU 390716 ● 2♀; Hermon Nature Reserve, Busheri curve, Plot F4; 33.301° N 35.773° E; 1791 m a.s.l.; 18 Jun. 2019; A. Dorchin, A. Sviri & Y. Mersman leg.; SMNHTAU 309206, 309279 ● 1♂; ibid.; SMNHTAU 309175 ● 1♂; Hermon Nature Reserve, Har ‘Ar’ar, Plot E6; 33.308° N 35.752° E; 1639 m a.s.l.; 18 Jun. 2019; A. Dorchin, A. Sviri & Y. Mersman leg.; SMNHTAU 309230 ● 1♀; Hermon NR, 300mN lower parking lot, Plot F1; 33.294° N 35.760° E; 1508 m a.s.l.; 28 May 2019; L. Friedman leg.; SMNHTAU 308133 ● 1♂; Mt. Hermon; 1500 m a.s.l.; 23 Apr. 1973; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; Mt. Meron; 1000 m a.s.l.; 16 Jun. 1971; ibid. ● 1♀; 20 km NE Qiryat Shemona, Hermon Cableway; 16 May 1996; C. Schmid-Egger leg.; CSE. – LEBANON ● 1♂; Al Montazah [Moutazah], nr. Mansourieh; 250 m a.s.l.; 30 Apr. 1996; C.G. Roche leg.;
Andrena cedricola
Wood, 2020:
High altitudes in the Levant (northern Israel, Lebanon, Syria) and Turkey, above 900 m. (
Mid-March to late May. The specimen from the Syrian part of the Golan Heights was incorrectly reported as being collected on 31 March 2001 in
Collected from Brassicaceae (Brassica, Peltaria). A single analyzed pollen load contained 100% Brassicaceae pollen (
ISRAEL ● 1♀; Har Hermon; 1600 m a.s.l.; 23 May 1998; A. Freidberg leg.; SMNHTAU 354883 ● 1♀; ibid.; 18 May 2009; L. Friedman leg.; SMNHTAU 34774 ● 3♂; Har Hermon; 33.2994° N 35.7675° E; 1645 m a.s.l.; 16 Apr. 2021; G. Pisanty leg.; SMNHTAU 361233, 361305, 361311 ● 1♂; ibid.; BOLD accession no. ANDIL494-25; SMNHTAU 361404 ● 1♂; ibid.; 33.300° N 35.767° E; 1620 m a.s.l.; 11 May 2020; SMNHTAU 334833 ● 1♂; ibid.; 33.292° N 35.7595° E; 1480 m a.s.l.; 7 Apr. 2021; pan trap; SMNHTAU 360842 ● 1♂; ibid.; 33.2992° N 35.7670° E; 1644 m a.s.l.; 16 Apr. 2022; SMNHTAU 390192 ● 7♀; Har Hermon, Nahal Guveta; 33.285° N 35.763° E; 1410 m a.s.l.; 11 May 2020; G. Pisanty leg.; on Peltaria angustifolia; SMNHTAU 334947, 334948, 334950, 334953 to 334956 ● 3♂; ibid.; SMNHTAU 334944 to 334946 ● 1♀; ibid.; BOLD accession no. ANDIL102-22; SMNHTAU 334951 ● 3♂; Har Meron; 1100 m a.s.l.; 17 Apr. 2000; A. Freidberg leg.; SMNHTAU 354890 to 354892 ● 1♀; Hermon; 33.298–9° N 35.767–70° E; 1640–1675 m a.s.l.; 19 May 2022; G. Pisanty leg.; on Brassicaceae; SMNHTAU 392777 ● 2♀; Hermon, Biq’at Man; 33.292° N 35.751° E; 1450 m a.s.l.; 29 Apr. 2022; G. Pisanty leg.; on Peltaria angustifolia; SMNHTAU 391528, 391529 ● 2♀; Hermon NR, 300mN lower parking lot, Plot F1; 33.294° N 35.760° E; 1508 m a.s.l.; 28 May 2019; L. Friedman leg.; SMNHTAU 308123, 308128 ● 1♀; Merom-Golan, N Golan Height; 1000 m a.s.l.; 23 Apr. 1997; R. Kasher leg.; SMNHTAU 354886 ● 1♀; Mt.Meron; 900 m a.s.l.; 13 Apr. 1988; I. Yarom leg.; SMNHTAU 354889 ● 1♂; ibid.; SMNHTAU 354887 ● 1♀; Neve-Ativ, 16km NE Qiryat-Shmona; 1000 m a.s.l.; 18 Apr. 1990; R. Kasher leg.; SMNHTAU 354882 ● 2♀; Qala’at Nemrod [Nimrod Castle]; 6 May 1987; A. Shlagman leg.; SMNHTAU 354884, 354885 ● 1♂; ibid.; SMNHTAU 367669 ● 1♀; 20 km NE Qiryat Shemona Hermon Cableway; 16 May 1996; C. Schmid-Egger leg.; CSE. – LEBANON ● 2♂; Beqaa, Rachaiya, 5 km S, Mount Hermon nature reserve; 33.4586° N 35.8395° E; 1500 m a.s.l.; 8 Apr. 2023; T. Wood leg.; TJWC ● 1♀,2♂; Mount Lebanon, Hazerta; 1400 m a.s.l.; 6 May 1996; C.G. Roche leg.;
Andrena oedicnema
Warncke, 1975a: 55–56, ♀ [Central Turkey:
Andrena (Micrandrena) oedicnema Warncke: Gusenleitner & Schwarz 2002: 550–551 (first description of ♂).
Mediterranean shrublands in Greece and the northern Middle East, including all countries of the Levant (
Mid-February to late April.
Collected from Apiaceae (Ferula) and Rosaceae (Pyrus).
IRAN ● 1♂; Fars province, Yasuj, Sarb-e Taveh; 2030 m a.s.l.; 4 May 2016; M. Kafka leg.; BOLD accession no. ANDGP021-25;
Andrena dividicincta
Pisanty, 2022:
Endemic to Mediterranean shrublands in the Levant (northern Israel, likely also Lebanon and Syria).
Late February to mid-April.
Polylectic, favouring flowering trees and shrubs such as Sapindaceae (Acer), Rosaceae (Prunus, Pyrus) and Rhamnaceae (
HOLOTYPE: ISRAEL ● 1♀; Montfort, Nahal Keziv [Montfort Castle, Nahal Kziv]; [33.04–05° N 35.22–23° E]; 28 Feb. 2018; G. Pisanty leg.; SMNHTAU 286301. – PARATYPES: ISRAEL ● 1♀; Har Hermon; 33.2992° N 35.7670° E; 1644 m a.s.l.; 16 Apr. 2022; G. Pisanty leg.; pan trap; SMNHTAU 390128 ● 10♀; ibid.; 33.2993° N 35.7678° E; 1650 m a.s.l.; on Acer monspessulanum; SMNHTAU 389829, 389831, 389834 to 389837, 389839, 389840, 389842, 389844 ● 1♀; ibid.; 33.2993° N 35.7679° E; 1649 m a.s.l.; 7 Apr. 2021; SMNHTAU 360308 ● 67♀; ibid.; 16 Apr. 2021; SMNHTAU 361544 to 361549, 361551 to 361564, 361566 to 361568, 361571 to 361574, 361576 to 361578, 361580, 361582 to 361584, 361586, 361587, 361589 to 361591, 361594 to 361597, 361599 to 361603, 361605 to 361609, 361611 to 361614, 361616, 361617, 361619 to 361622, 361624 to 361626, 361629 ● 2♂; ibid.; SMNHTAU 361489, 361497 ● 1♂; Har Meron; 800 m a.s.l.; 5 Mar. 2011; A. Freidberg leg.; BOLD accession no. ANDIL018-22; SMNHTAU 89140 ● 11♀; Hermon; 33.2992° N 35.7668° E; 1642 m a.s.l.; 16 Apr. 2022; G. Pisanty leg.; on Rosaceae; SMNHTAU 389948 to 389958 ● 7♀; ibid.; 33.2993° N 35.7670° E; 1641 m a.s.l.; on Prunus dulcis; SMNHTAU 389929 to 389935 ● 9♀; Meron JNC., Upper Galilee; 20 Mar. 1995; on Pyrus syriaca; SMNHTAU 367625 to 367633 ● 1♀; Monfort; 10 Mar. 1981; F. Kaplan leg.; SMNHTAU 348525 ● 1♀; Montfort; 2 Mar. 1987; A. Freidberg leg.; SMNHTAU 348526 ● 1♀; ibid.; A. Shlagman leg.; SMNHTAU 348527 ● 2♀; Montfort; 4 Mar. 1993; A. Freidberg leg.; SMNHTAU 348528, 348529 ● 1♀; ibid.; 5 Mar. 2008; BOLD accession no. ANDIL108-22; SMNHTAU 348531 ● 3♀; Montfort, Nahal Keziv; 28 Feb. 2018; G. Pisanty leg.; SMNHTAU 286240, 286273, 286274 ● 1♀; Nahal Keziv; 33°02.7’ N 35°13.6’ E; 5 Mar. 2008; A. Freidberg leg.; SMNHTAU 348530 ● 1♀; Nahal Keziv; 33.0465° N 35.226° E; 26 Feb. 2021; G. Pisanty leg.; SMNHTAU 357679 ● 1♂; Nahal Keziv, Montfort; 33.046° N 35.227° E; 200 m a.s.l.; 28 Feb. 2018; G. Pisanty leg.; SMNHTAU 336223 ● 1♀; ibid.; 33°02’N 35°14’ E; 400 m a.s.l.; 24 Feb. 2011; A. Freidberg leg.; SMNHTAU 90953 ● 1♀; Sasa; 20 Apr. 2015; O. Winberger leg.; SMNHTAU 184802. – non-type material: ISRAEL ● 1♂; Har Hermon; 33.2855° N 35.763° E; 1420 m a.s.l.; 7 Apr. 2021; G. Pisanty leg.; pan trap; SMNHTAU 360687 ● 1♂; ibid.; 33.300° N 35.767° E; 1610 m a.s.l.; SMNHTAU 360519 ● 2♀; ibid.; 33.299° N 35.769° E; 1650 m a.s.l.; sweep; SMNHTAU 360374, 360375.
Andrena extenuata
Wood & Monfared, 2022: 21–25, ♀♂ [Iran:
High elevations above 1400 m in Syria and Iran.
Late February to late April.
Collected from flowering trees of the families Rosaceae (Prunus, Pyrus) and Sapindaceae (Acer) (
PARATYPES: SYRIA ● 1♀,14♂; Bludan [Bloudan], 57 km NW of Damascus; 2000 m a.s.l.; 24 Apr. 1992; K. Warncke leg.;
Andrena pandosa
Warncke, 1968b: 72, ♀♂ [Algeria:
Andrena pandosa ssp. excelsa
Warncke, 1974b: 14, 41, ♀♂ [Libya:
Andrena pandosa ssp. graciosa
Warncke, 1993: 762, ♀♂ [Canary Islands:
South Mediterranean. In the Levant, occurring in semi-arid to desert habitats in Israel, the West Bank and Jordan (
Mid-February to early May.
Narrowly oligolectic on Reseda (Resedaceae) (
ISRAEL ● 1♀; Beersheba; 1 Apr. 19[??]; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; ibid.; 15 Apr. 1970; “Andrena pandosa ssp. antigua War.” paratype label ● 1♀; En Geddi; 2 Mar. [19]71; ibid. ● 3♀; Jer[usalem?]; 2 May [19]40; “Andrena pandosa ssp. antigua War.” paratype label; SMNHTAU ● 1♂; Jerusalem; 27 Mar. 1941; H. Bytinski-Salz leg.; SMNHTAU ● 1♀; ibid.; 1 Apr. 1941 ● 2♀,1♂; ibid.; 7 Apr. 1947 ● 1♂; ibid.; 7 Mar. [19]40; “Andrena pandosa ssp. antigua War.” paratype label ● 3♂; Jerusalem; 19 Apr. 1953; J. Wahrman leg.; cave; SMNHTAU ● 1♂; ibid.; 19 Apr. 1945; “Andrena pandosa ssp. antigua War.” paratype label ● 1♀; Jerusalem, Mt. Scopus; 2 May 1940; “Andrena pandosa ssp. antigua War.” paratype label; SMNHTAU ● 1♀,7♂; ibid.; 19 Apr. 1945 ● 1♂; on Malva sylvestris ● 1♀; Ma’agar Yeroham, NW, Nahal Revivim; 460 m a.s.l.; 5 Apr. 2017; L. Friedman leg; SMNHTAU 270759 ● 1♀; Mishor Rotem; 15 Mar. [19]66; M. Weichselfish leg.; SMNHTAU ● 1♂; ibid.; 7 Mar. [19]65; on Helianthemum stipulatum; SMNHTAU 367690● 1♀; Ramon; 10 Mar. 1974; D. Furth leg.; SMNHTAU 367689 ● 1♂; Tel ‘Eton; 31.492° N 34.925° E; 3 Apr. 2022; G. Pisanty leg.; sweeping; SMNHTAU 388466. – JORDAN ● 1♂; S of Irbid; 13 Apr. 2009; M. Snižek leg.; TJWC ● 1♀; 10 km N, NE of Jarash [Jerash]; 20 Apr. 2002; ibid. ● 1♀; 15 km W Jerash, Dibbin; 2 May 2006; K. Deneš leg.; TJWC ● 5♀; 15 km E of Petra; 26 Apr. 2008; K. Deneš leg.;
Melitta proxima
Kirby, 1802 (nec Andrena proxima Smith 1847): 146–147, ♀ [England:
Melitta digitalis
Kirby, 1802: 159–160, ♀ [England:
Andrena aspericollis
Pérez, 1895: 37, ♀♂ [Algeria:
Broadly across the Western Palaearctic, but excluding the most Atlantic parts, mostly in mesic habitats (
In Europe: one generation, mid-April to late June.
Broadly oligolectic on Apiaceae. Also visits Asteraceae, Brassicaceae, Campanulaceae and Euphorbiaceae (
LEBANON ● 2♀; Mount Lebanon Governorate, Kesrouane, Jabal Moussa Biosphere Res.; 1400 m a.s.l.; 14 May 2023; V. Soon leg.;
Andrena yelkouan
Warncke, 1975a: 97–98, ♀♂ (♂ stylopized) [SE Turkey:
Andrena yelkouan Warncke: Gusenleitner & Schwarz 2002: 838–839 (first description of non-stylopized ♂).
Northern Middle East. Records from Central Asia are refuted – these originate from a misinterpretation by Osytschnjuk et al. (2008), who describe the male as having a yellow clypeus. In the Levant, present in Mediterranean shrubland, semi-desert and desert habitats in Israel, the West Bank, Jordan and Syria (Wood & Monfared 2022).
Mid-February to mid-May.
Collected from Brassicaceae and Fabaceae (Trifolium).
PARATYPES: WEST BANK ● 1♀; Jericho; 25 Mar. 1941; H. Bytinski-Salz; head missing; SMNHTAU ● 2♀; Jericho; 7 Apr. 1970; H. Bytinski-Salz; SMNHTAU ● 1♀; JerichoWQ; 18 Feb. 1971; H. Bytinski-Salz; head missing; SMNHTAU ● 1♀; OldJerichoRd; 5 Apr. 1947; ibid. – non-type material: ISRAEL ● 1♀; Giv’at Oz; 10 Apr. 1988; I. Yarom leg.; SMNHTAU 348543 ● 1♀; Har Harif, Rt. 10, N junction; 30°32’ N 34°33’ E; 11 Apr. 2002; L. Friedman leg.; SMNHTAU ● 1♂; Har Meron Reserve, Camping under Kefar Meron; 32°58’ N 35°26’ E; 600 m a.s.l.; 25 Apr. 2002; L. Friedman leg.; SMNHTAU 353520 ● 3♀; Har Ramon; 30.503° N 34.636° E; 1030 m a.s.l.; 9 Apr. 2024; L. Friedman leg.; SMNHTAU 449906, 449908, 449914 ● 1♂; Hare Gilboa’, Har Ahino’am; 32.502° N 35.414° E; 450 m a.s.l.; 20 Mar. 2012; L. Friedman leg.; SMNHTAU 120855 ● 1♂; Kokhav HaYarden; 25–27 Mar. 2001; L. Friedman leg.; Vinegar pitfalls; SMNHTAU 207212 ● 1♀; Ma’agar Yeroham; 7 Mar. 2007; A. Freidberg leg.; SMNHTAU 348545 ● 2♀; Moradot HaGolan NR, 960m SE Gonen; 33.111° N 35.651° E; 190 m a.s.l.; 7 Apr. 2019; A. Dorchin, A. Sviri & O. Halbershtat leg.; SMNHTAU 308878, 308879 ● 1♂; ibid.; SMNHTAU 308877 ● 1♂; Mt. Carmel, Etzbah; 9 Apr. 1999; S.P.M. Roberts leg.; SPMR ● 1♂; Nahal Bezeq; 32.410° N 35.441° E; 2 m a.s.l.; 15 Mar. 2021; A. Dorchin leg.; SMNHTAU 358704 ● 14♀; Nahal Boqer; 30.906–19° N 34.762–74° E; 10 Mar. 2023; G. Pisanty leg.; SMNHTAU 423940 to 423948, 423950 to 423954 ● 1♂; Nahal Dishon; 1 Apr. 1991; R. Kasher leg.; SMNHTAU 353511 ● 1♀; Nahal Kelah; 32.744° N 35.023° E; 10 Apr. 2017; G. Pisanty leg.; on Brassicaceae; SMNHTAU 270483 ● 1♀; Nahal Loz; 30.492° N 34.631° E; 13 Apr. 2020; G. Pisanty leg.; BOLD accession no. ANDIL325-22; SMNHTAU 334094 ● 1♀; NahalMe’arot; 8 Apr. 1988; I. Yarom leg.; SMNHTAU 348544 ● 4♀; Park Britannia; 20 Apr. 2015; T. Chaprazaro leg.; SMNHTAU 185251, 185254, 185263, 185265 ● 1♀; ibid.; BOLD accession no. ANDPH028-21; SMNHTAU 185249 ● 1♀; Park Britanya; 15 Apr. 2011; T. Koznichki leg.; on Trifolium purpureum; SMNHTAU 270479 ● 1♀; Ras Zuweira, Negev-E; 19 Mar. 1946; SMNHTAU ● 2♀; Rekhes HaSullam; 33.091° N 35.112° E; 80 m a.s.l.; 18 Mar. 2025; G. Pisanty leg.; SMNHTAU 465062, 465063 ● 1♂; Ya’ar Nehosha; 22 Mar. 2016; T. Chaprazaro leg.; SMNHTAU 251443 ● 1♂; Yerushalayim; 8 Mar. 2015; T. Jumah leg.; BOLD accession no. ANDIL209-22; SMNHTAU 217996 ● 1♂; Zomet Haela; 4 Apr. 1999; O. Greif leg.; SMNHTAU 367665. – JORDAN ● 2♀; Al Karak [Kerak] env; 6 Apr. 2013; M. Snižek leg.;
Notes for using the keys:
1. Some species are extremely challenging to separate, due to presence of minute interspecific differences together with strong intraspecific variation. In these cases, access to confidently determined reference material is essential, and distribution and relative abundance of both sexes should be used to inform identifications. Often, 100% confidence in identification is possible only with DNA barcoding. The following couplets are especially challenging: female key – 35, 37, 38, 41–42; male key – 32–33, 38.
2. Pay close attention to the terminology of tergal areas. Terga, tergal discs and tergal marginal zones are distinct terms, and often there are structural differences between basal versus apical parts of the tergal disc itself, not referring to the tergal marginal zone.
3. Male genital capsules are illustrated for all 41 species whose male sex is known (all species except Andrena herodesi). When using the male key, always consult the shape of the genitalia (even when not specifically indicated in the couplet) to make sure your identification is correct.
4. Some diagnostic characters become less reliable in aged or worn-out specimens. This especially concerns integumental colour, hair colour, and hair density. In such cases, if possible, species inference should be based more on sculpturing rather than colour and pubescence.
The following abbreviations are used throughout the keys: F – flagellomere, T – metasomal terga.
Females
| 1 | Propodeal triangle completely finely reticulated, without any rugosity, at most with few mediobasal wrinkles (Fig. |
2 A. longibarbis group |
| 1’ | Propodeal triangle weakly to strongly rugose or rugose-areolate, at least basally at junction with metanotum (Fig. |
8 |
| 2 (1). | Clypeus very smooth and shiny at least in apical half (Fig. |
3 |
| 2’ | Clypeus with longitudinal striations reaching almost to its apex (Fig. |
6 |
| 3 (2). | Scutellum very shiny, superficially shagreened to smooth, strongly contrasting with shagreened and matt scutum (Fig. |
A. govinda Warncke |
| 3’ | Scutellum matt and distinctly shagreened, similar to scutum. Other traits variable. Body length 6–8 mm | 4 |
| 4 (3). | Clypeus weakly arched. F4–10 orange. Tergal marginal zones strongly orange basally, clearly demarcated from neighbouring disc. Tergal hair bands broad (Fig. |
A. mariana Warncke s.s. |
| 4’ | Clypeus flat. F4–10 dark brown to reddish-brown anteriorly. Tergal marginal zones usually more reddish-brown basally, more weakly contrasting with neighbouring disc. Tergal apical hair bands relatively narrow, limited to apical half of marginal zone, those on T2–3 interrupted, on T4 continuous (Fig. |
5 |
| 5 (4). | Basal ¼–½ of clypeus with longitudinal striations. Labral process subquadrate (Fig. |
A. leptura Warncke stat. nov. |
| 5’ | Basal ¼–½ of clypeus shagreened, without longitudinal striations. Labral process narrow, somewhat longer than broad (Fig. |
A. kugleri Pisanty sp. nov. |
| 6 (2). | Hind leg with pretarsal claws unidentate. Labral process concave, about as long as broad, arched laterally and pointed apically (Fig. |
A. decollata Warncke |
| 6’ | Hind leg with pretarsal claws bidentate. Labral process flat, triangular or trapezoidal (Fig. |
7 |
| 7 (6). | Labral process trapezoidal, distinctly broader than long. Clypeus flat to slightly concave centrally, longtidunal striation very fine and shallow (Fig. |
A. herodesi Pisanty & Wood |
| 7’ | Labral process more or less triangular, about as long as broad. Clypeus slightly convex centrally, never with a concave impression, longitudinal striation strong (Fig. |
A. longibarbis Pérez |
| 8 (1). | Clypeus completely flat, shagreened on basal ⅔, smooth near apex (Fig. |
A. yelkouan Warncke |
| 8’ | Clypeus at least slightly domed or apically elevated, and/or propodeal triangle more coarsely or extensively rugose (Fig. |
9 |
| 9 (8). | Facial foveae uniformly broad, not narrowed ventrally, occupying ½ paraocular area width (Fig. |
A. pandosa Warncke |
| 9’ | Facial foveae narrower, at least ventrally, not occupying ½ paraocular area width. Propodeal triangle usually more extensively and/or coarsely rugose | 10 |
| 10 (9). | Body length 9–10 mm. Surface of propodeal corbicula with star-shaped wrinkles (Fig. |
A. proxima (Kirby) |
| 10’ | Body length 5–8 mm. Surface of propodeal corbicula finely reticulated, very rarely with star-shaped wrinkles. Clypeus variably sculptured, but not with strong coarse transverse wrinkles (in some species with weaker transverse wrinkles). Labral process, scutum and propodeal triangle with variable sculpture | 11 |
| 11 (10). | Discs of T2–4 very shiny, weakly shagreened to smooth, punctation absent or weak and sparse. T2–3 with apical hair bands broadly interrupted, arising from the apical half of the marginal zone (Fig. |
12 |
| 11’ | Discs of T2–4 with variable sculpture, strongly shagreened and/or strongly and densely punctate; never strongly shining without punctures or with weak and sparse punctures. T2–3 apical hair bands often more narrowly interrupted and/or arising from the base of the marginal zone. Body length 5–8 mm | 14 |
| 12 (11). | Labral process very broad, arched (Fig. |
A. dividicincta Pisanty |
| 12’ | Labral process very narrow, more or less triangular (Fig. |
13 A. oedicnema group |
| 13 (12). | Clypeus with weak transverse striations (most visible in basal ½), punctation dense and relatively coarse, distance between punctures 1 puncture diameter. Labral process rounded apically (Fig. |
A. oedicnema Warncke |
| 13’ | Clypeus without transverse striations, punctation sparse and relatively fine, distance between punctures 2 puncture diameters. Labral process pointed apically (Fig. |
A. cedricola Wood |
| 14 (11). | Facial foveae extremely narrow along their entire length, narrower than the width of a flagellum (Fig. |
A. extenuata Wood |
| 14’ | Without this combination of characters; facial foveae almost always broader, if in doubt then terga strongly and densely punctate | 15 A. minutula group |
| 15 (14). | Discs of T1–4 smooth AND strongly and densely punctured (Fig. |
16 |
| 15’ | Discs of T2–3 and often also T1 and T4 mostly shagreened, punctation variable, usually weaker | 17 |
| 16 (15). | Discs of T2–4 very densely and coarsely punctate, distance between punctures 0–0.5 puncture diameters, marginal zones more or less impunctate (Fig. |
A. magunta Warncke |
| 16’ | Discs of T2–4 more sparsely and finely punctate, distance between punctures 0.5–1 puncture diameters, marginal zones distinctly finely punctured (Fig. |
A. luscinia Warncke |
| 17 (15). | Clypeus polished-smooth at least on apical half (Fig. |
18 |
| 17’ | Apical half of clypeus at least weakly shagreened or transversely wrinkled, never polished-smooth between the punctures. Found at various altitudes | 22 |
| 18 (17). | Body length 5 mm. Terga essentially impunctate. Scutum shagreened to partly smooth, shiny, distance between punctures 0.5–1.5 puncture diameters (Fig. |
A. tringa Warncke |
| 18’ | Body length 6.5–8 mm. Tergal discs at least weakly punctured (Fig. |
19 |
| 19 (18). | Disc of T1 smooth and polished between punctures, contrasting shagreened sculpture of discs of T2–3. Tergal discs finely and densely punctate, punctures separated by 0.5–1 puncture diameters (Fig. |
A. enslinella Stöckhert |
| 19’ | Disc of T1 shagreened, not sculpturally differing from discs of T2–3. Tergal discs either more sporadically punctate (punctures separated by 0.5–3 puncture diameters, Fig. |
20 |
| 20 (19). | Tergal discs strongly and coarsely punctured, punctures separated by ≤0.5 puncture diameters (Fig. |
A. libanica Wood sp. nov. |
| 20’ | Tergal discs sporadically punctate, punctures separated by 0.5–3 puncture diameters (Fig. |
21 |
| 21 (20). | Terga with comparatively strong microreticulation, punctures of tergal discs relatively shallow and obscure, somewhat disappearing into underlying sculpture (Fig. |
A. alshaykh Pisanty sp. nov. |
| 21’ | Terga with comparatively weak shagreen, shining, punctures of tergal discs stronger, always with at least some distinct punctures across the central and lateral parts of the disc (Fig. |
A. lindbergella Pittioni |
| 22 (17). | Surface of clypeus roughened by distinct transverse striations and/or oblique punctures, at least in basal half (Figs |
23 |
| 22’ | Clypeus smooth to finely shagreened, at most with hint of transverse striations (Figs |
30 |
| 23 (22). | Flagellum distinctly orange anteriorly (in fresh specimens). Body length 6–6.5 mm | 24 |
| 23’ | Flagellum entirely dark. Body length 5–7.5 mm | 25 |
| 24 (23). | Posterior ¾ of scutum polished-smooth, strongly punctured (Fig. |
A. calandra Warncke |
| 24’ | Scutum entirely shagreened, superficially punctured (Fig. |
A. convexifrons Wood |
| 25 (23). | Basal half of clypeus transversely striated, very densely punctured, distance between punctures 0–1 puncture diameters, usually with narrow impunctate midline. Apical half of clypeus shagreened to smooth, without striations, more sparsely punctured (Fig. |
A. alfkenelloides cardalia Warncke |
| 25’ | Clypeus different, usually more uniformly sculptured (Figs |
26 |
| 26 (25). | Disc of T1 weakly shagreened to smooth, distinctly finely punctured (Fig. |
A. friedmani Pisanty sp. nov. |
| 26’ | Disc of T1 strongly shagreened and/or impunctate, punctation hardly discernible against underlying sculpture. Other traits variable | 27 |
| 27 (26). | Scutum finely, very densely punctured, distance between punctures about 0.5 puncture diameter, underlying surface matt, with strong granular shagreening (Fig. |
A. rugothorace Warncke |
| 27’ | Scutum more sparsely and/or more coarsely and obliquely punctured, underlying surface matt to partly shiny (Fig. |
28 |
| 28 (27). | Scutum dull, strongly and densely punctured, some punctures with raised margins (crater-like punctures) medially (Fig. |
A. aspera Pisanty & Wood sp. nov. |
| 28’ | Centre of scutum usually without punctures with raised margins (Fig. |
29 |
| 29 (28). | Clypeus not much broader than long, shagreened and matt, with weak transverse striations (Fig. |
A. stolida Warncke (in part) |
| 29’ | Clypeus distinctly broader than long, distinctly transversely striated (Fig. |
A. paganettina Warncke |
| 30 (22). | Tergal marginal zones lightened orange-hyaline. Tergal hair bands broad and conspicuous, extending onto the bases of the subsequent terga (Fig. |
A. sulfurea Wood |
| 30’ | Tergal marginal zones darker, tergal hair bands narrower. Scutum variable | 31 |
| 31 (30). | Discs of T2–4 distinctly and densely punctate, punctures small but dense, separated by 0.5–1 puncture diameters, punctures not or only very irregularly extending onto marginal areas. Disc of T1 with punctures much more obscure (Fig. |
A. alfkenella Perkins |
| 31’ | Punctation of T2–4 discs sparser and weaker, if any | 32 |
| 32 (31). | Labral process snout-shaped, slightly constricted medially (Fig. |
A. lunaris Pisanty & Wood |
| 32’ | Labral process not snout-shaped. Scutal punctation usually sparser, not obscured by dense pubescence arising from the punctures. Clypeus sculpture variable | 33 |
| 33 (32). | Apical flagellomeres distinctly orange (in fresh specimens). Wing veins yellowish-golden (Fig. |
A. tkalcui Gusenleitner & Schwarz |
| 33’ | Apical flagellomeres reddish-brown to black. Wing veins light to dark brown (Fig. |
34 |
| 34 (33). | Labral process large, trapezoidal. Clypeus protuberant apically, strongly transversely arched, fully shagreened, very weakly, sparsely punctured (Fig. |
A. phoenicia Pisanty sp. nov. |
| 34’ | Labral process smaller and/or clypeus flatter or differently sculptured. Scutum and scutellum variable | 35 |
| 35 (34). | Discs of T3 and often also T2 distinctly smoother apically vs. basally, the tight shagreening of basal areas apically disintegrating into irregular, dense fine punctation. Clypeus domed, fully shagreened and matt (Fig. |
A. hebraica Pisanty & Wood sp. nov. |
| 35’ | Discs of T2–3 uniformly, fully shagreened and impunctate. Clypeus domed to centrally flattened, shagreened to shiny. Scutum shagreened to smooth | 36 |
| 36 (35). | Scutum shagreened to weakly shiny, finely and not very densely punctured, distance between punctures about 1 puncture diameter, punctation usually not very strong (Fig. |
37 |
| 36’ | Scutum shagreened to smooth, punctation stronger and/or denser (Figs |
38 |
| 37 (36). | Scutum entirely shagreened and matt, punctation very weak, often hardly discernible. Clypeus weakly punctured, flattened medially, weakly shagreened throughout. (Israeli coastal plain) | A. tiaretta Warncke |
| 37’ | Scutum shagreened to partly smooth, punctation usually distinct. Clypeus usually smoother apically vs. basally (Levant and Cyprus, widespread) | A. spreta Pérez |
| 38 (36). | Scutum and scutellum shagreened and dull, distance between punctures 0.5–1 puncture diameters, punctation usually weak, in Levantine populations often hardly discernible (Fig. |
A. cervina Warncke |
| 38’ | Scutum and scutellum shagreened to smooth, punctation stronger and/or sparser (Fig. |
39 |
| 39 (38). | Cypriot bees. Scutellum and often scutum distinctly shiny, distance between punctures 0.5–1.5 puncture diameters (Fig. |
A. aphroditae Pisanty sp. nov. |
| 39’ | Levantine bees. Different trait combination | 40 |
| 40 (39). | Scutum partly shagreened (1st generation) to almost smooth (2nd generation), relatively sparsely punctured, punctures slightly irregular, separated by 1–2 puncture diameters (Fig. |
A. minutuloides Perkins |
| 40’ | Scutum densely punctured (distance between punctures 0.5–1 puncture diameters, Fig. |
41 |
| 41 (40). | Clypeus strongly domed, strongly granularly shagreened, often with hint of transverse striation, punctation fine, distance between punctures 1–2 puncture diameters, with ill-defined narrow impunctate midline (Fig. |
A. stolida Warncke (in part) |
| 41’ | Clypeus differently sculpted, either more flattened and/or more finely shagreened and/or more coarsely punctured (Fig. |
42 |
| 42 (41). | Clypeus punctation relatively weak, sparse and fine, distance between punctures 1–3 puncture diameters, at most with ill-defined impunctate midline (Fig. |
A. sillata Warncke |
| 42’ | Clypeus punctation stronger, denser and coarser, distance between punctures 1–2 puncture diameters, often with strong impunctate midline (Fig. |
A. chananaea Pisanty & Wood sp. nov. |
Andrena (Micrandrena) females, propodeal triangles (A–C), facial foveae (D), clypei (E–I), scuta and scutella (J) and metasomae (K–P). A, I, P A. longibarbis; B A. yelkouan; C A. alfkenelloides cardalia; D, E, M A. leptura; F A. kugleri; G, N A. decollata; H, O A. herodesi; J, K A. govinda; L A. mariana.
Andrena (Micrandrena) females, clypei (A–F), scuta and scutella (G–K) and first terga (L). A A. alfkenelloides cardalia, 2nd generation; B, H, L A. friedmani; C, I A. rugothorace; D, J A. aspera; E A. stolida (rugose variant); F, K A. paganettina; G A. alfkenelloides cardalia, 1st generation.
Males
| 1 | Anterior margin of clypeus more or less flat, apicolateral corners prominent in frontal view. Clypeus smooth over majority of surface, strongly and coarsely punctured (Fig. |
A. pandosa Warncke |
| 1’ | Anterior margin of clypeus strongly curved, apicolateral corners rather obscured in frontal view. Different trait combination | 2 |
| 2 (1). | Propodeal triangle completely covered with fine reticulation, without any rugosity, at most with few mediobasal wrinkles (Fig. |
3 A. longibarbis group |
| 2’ | Propodeal triangle weakly to strongly rugose or rugose-areolate, at least basally at junction with metanotum (Fig. |
8 |
| 3 (2). | Clypeus longitudinally striated almost to its apex (Fig. |
A. decollata Warncke |
| 3’ | Clypeus smooth and shiny at least in its apical half (Fig. |
4 |
| 4 (3). | Apex of clypeus with long white hairs, in fresh specimens these hairs almost obscuring its apical margin (Fig. |
A. longibarbis Pérez |
| 4’ | Apex of clypeus normally haired, hairs at apex of clypeus not noticeably longer or denser than elsewhere. Penis valves normally developed, not bladder-shaped (but may be relatively broad). Gonostyli weakly broadened apically, apex rounded (Fig. |
5 |
| 5 (4). | Scutellum shiny and almost smooth, contrasting dull sculpture of scutum (Fig. |
A. govinda Warncke |
| 5’ | Scutellum matt and distinctly shagreened, dull, sculpture similar to scutum. Other traits variable. Body length 5.5–7 mm | 6 |
| 6 (5). | Penis valves relatively broad basally (Fig. |
A. leptura Warncke stat. nov. |
| 6’ | Penis valves narrow throughout (Fig. |
7 |
| 7 (6). | F2–11 orange ventrally. Tergal marginal zones distinctly orange throughout, sharply contrasting with darker tergal discs, without a transition zone (Fig. |
A. mariana Warncke s.s. |
| 7’ | F2–11 light brown ventrally. Tergal marginal zones reddish-orange basally, whitish apically, gradually blending into darker tergal discs (Levant) | A. kugleri Pisanty sp. nov. |
| 8 (2). | Scutum very densely and coarsely, obliquely punctured (Fig. |
A. proxima (Kirby) |
| 8’ | Scutum without oblique punctures, clypeus with weaker and finer transverse striation or none at all. Body length 4–9 mm. Other traits variable | 9 |
| 9 (8). | Discs of T2–4, at least in apical half, very shiny, weakly shagreened to mirror-smooth AND finely and sparsely punctured, distance between punctures >2 puncture diameters (Fig. |
10 |
| 9’ | Discs of T2–4 more strongly shagreened and/or more densely and coarsely punctured. Body length 4–9 mm | 12 |
| 10 (9). | Gonocoxites with their inner margins diverging apically, with strong, rounded dorsal lobes. Gonostyli short, strongly curved, with pronounced inner angle. Penis valves broad (Fig. |
A. dividicincta Pisanty |
| 10’ | Gonocoxites with their inner margins parallel-sided, dorsal lobes more weakly developed. Gonostyli elongate, penis valves narrow, genital shape resembling a Greek lyre (Fig. |
11 A. oedicnema group |
| 11 (10). | Scutum shiny, strongly and relatively coarsely punctured, punctures with raised margins (Fig. |
A. oedicnema Warncke |
| 11’ | Scutum finely shagreened, more weakly shiny, more weakly and finely punctured, punctures usually without raised margins (Fig. |
A. cedricola Wood |
| 12 (9). | Gonostyli strongly elongate, dorsal gonocoxite lobe absent (Fig. |
13 |
| 12’ | Gonostyli not so elongate, dorsal gonocoxite lobe absent or present (Figs |
14 A. minutula group |
| 13 (12). | Clypeus completely flat. F2–11 reddish ventrally. Gonostyli more or less straight (Fig. |
A. yelkouan Warncke |
| 13’ | Clypeus weakly domed. Flagellum entirely dark. Basal half of gonostylus strongly incurved, apical half parallel-sided (Fig. |
A. extenuata Wood |
| 14 (12). | F2–11 reddish-orange ventrally. Body length 4.5–6 mm | 15 |
| 14’ | F2–11 brown, grey or black throughout. Body length 4–9 mm | 18 |
| 15 (14). | Dorsal gonocoxite lobe strongly developed, rounded (Fig. |
16 |
| 15’ | Dorsal gonocoxite lobe weak to absent (Fig. |
17 |
| 16 (15). | F1 about as long as 3, at most 1.1 times longer. Tergal hairbands relatively narrow. Genital capsule somewhat elongate, gonostyli whitish apically (Fig. |
A. tkalcui Gusenleitner & Schwarz |
| 16’ | F1 at least 1.5 times longer than 3. Tergal hairbands broad, strongly extending onto disc of subsequent tergum (Fig. |
A. sulfurea Wood |
| 17 (15). | Scutum completely smooth (Fig. |
A. calandra Warncke |
| 17’ | Scutum and terga strongly shagreened and matt (Fig. |
A. convexifrons Wood |
| 18 (14). | Apical margin of gonocoxite pointed, often produced into distinct dorsal lobe, never truncate (Fig. |
19 |
| 18’ | Apical margin of gonocoxite truncate to slightly rounded, without distinct dorsal lobe (Figs |
28 |
| 19 (18). | F1 about as long as 3, at most 1.1 times longer. Genitalia simple, dorsal gonocoxite lobe small (Fig. |
A. spreta Pérez |
| 19’ | F1 at least 1.3 times longer than 3. Other traits variable | 20 |
| 20 (19). | Scutum smooth centrally. Dorsal gonocoxite lobe elongate and pointed, gonostyli simple, finger-shaped, penis valves relatively narrow (Fig. |
A. friedmani Pisanty sp. nov. |
| 20’ | Scutum shagreened across its whole surface. Genitalia different. Flagellomere proportions variable | 21 |
| 21 (20). | Tergal discs distinctly punctured, distance between punctures 1–2 puncture diameters (Fig. |
22 |
| 21’ | Tergal discs impunctate or very obscurely punctured, punctation hardly discernible from underlying shagreening. Apical half of clypeus at least weakly shagreened or transversely wrinkled, and/or weakly punctured. Found in diverse habitats | 24 |
| 22 (21). | Gonostyli suddenly converging medially, with a resulting kink in both the inner and outer margins (Fig. |
A. alshaykh Pisanty sp. nov. |
| 22’ | Gonostyli weakly, uniformly curved, without an obvious kink in either the inner or outer margins (Fig. |
23 |
| 23 (22). | Terga strongly and densely punctate, punctures somewhat coarse and separated by <0.5–0.5 puncture diameters (Fig. |
A. libanica Wood sp. nov. |
| 23’ | Terga finely and slightly more sparsely punctate, punctures separated by 0.5–1 puncture diameters (Fig. |
A. lindbergella Pittioni |
| 24 (21). | Outer margin of gonostylus with strong inward kink near apex (Fig. |
25 |
| 24’ | Outer margin of gonostylus without strong inward kink near apex (Fig. |
27 |
| 25 (24). | Scutum finely shagreened, punctation extremely weak, hardly discernible. Genitalia relatively slender (Fig. |
A. cervina Warncke |
| 25’ | Scutum with strong grainy shagreening, at least some punctures distinct against this underlying sculpture. Genitalia broader (Fig. |
26 |
| 26 (25). | Dorsal gonocoxite lobes, when viewed together, broader than width of visible base of penis valves (Fig. |
A. phoenicia Pisanty sp. nov. |
| 26’ | Dorsal gonocoxite lobes, when viewed together, slightly narrower than width of visible base of penis valves (Fig. |
A. stolida Warncke |
| 27 (24). | Clypeus transversely striated at least in basal ½. F1 about as long as 2+3. Penis valves narrow, slightly broadening close to visible base (Fig. |
A. rugothorace Warncke |
| 27’ | Clypeus not striated, at most with slight wrinkles basolaterally. F1 distinctly shorter than 2+3. Penis valves broad basally, occupying ½ space between gonostyli, strongly tapering to strong contraction at mid-point, apical half very narrow (Fig. |
A. lunaris Pisanty & Wood |
| 28 (18). | Discs of T2–4 smooth AND distinctly punctured, at least on apical half (Fig. |
29 |
| 28’ | Discs of T2–4 mostly shagreened throughout and/or obscurely punctured to impunctate. Body length 4–7 mm | 34 |
| 29 (28). | Ocelloccipital distance about 2 times the diameter of a lateral ocellus (Fig. |
A. magunta Warncke |
| 29’ | Ocelloccipital distance more or less equal to the diameter of a lateral ocellus. Terga and scutum variable | 30 |
| 30 (29). | F1 as long as 2+3 or slightly longer. Body length 8–9 mm. Genital capsule distinctive, gonostyli thick and robust, strongly contrasting extremely narrow penis valves, penis valves produced to very narrow stiletto-like points between broad flattened apical parts of gonostyli (Fig. |
A. enslinella Stöckhert |
| 30’ | F1 distinctly shorter than 2+3. Body length 5–6.5 mm. Genital capsule different | 31 |
| 31 (30). | Marginal zone of T2 and to a lesser extent T3 distinctly and finely punctured. Entire surface of terga completely smooth (Fig. |
A. luscinia Warncke |
| 31’ | T2–3 with marginal zones mostly impunctate. Surface of terga often with partly shagreened areas | 32 |
| 32 (31). | Gonostyli almost parallel-sided, only slightly narrowing basally. Penis valves distinctly broader basally vs. apically (Fig. |
A. chananaea Pisanty & Wood sp. nov. (in part) |
| 32’ | Gonostyli with inner margins more strongly narrowing basally. Penis valves more uniformly narrow (Fig. |
33 |
| 33 (32). | 1st generation (black to dark facial hair) with clypeus densely punctate, often with transverse striations basally, clypeus generally dull. 2nd generation (pale facial hair) with clypeus densely punctate, punctures almost confluent, interspaces dull. F1 usually 1.0–1.2 times longer than 2, often shorter than 3. Body length 5–6.5 mm (Levant and Cyprus, scrubland, widespread) | A. alfkenelloides cardalia Warncke (in part) |
| 33’ | 1st generation (black facial hair) with clypeus comparatively more sparsely punctate, therefore more strongly shining, never with transverse striations. 2nd generation (pale facial hair) with clypeus comparatively more sparsely punctate, punctures separated by up to 1 puncture diameter, interspaces polished and shining. F1 usually about 1.5 times longer than 2, rarely shorter than 3. Body length 6–6.5 mm (Lebanon, above 1300 m) | A. alfkenella Perkins |
| 34 (28). | Gonostyli with both inner and outer margins strongly curved inwards, apexes somewhat truncate. Penis valves broad, at maximum width (submedially) occupying more than ½ space between gonostyli (Fig. |
A. sillata Warncke |
| 34’ | Gonostyli not strongly curved inwards (Fig. |
35 |
| 35 (34). | Penis valves narrow basally, slightly broadening medially close to visible base (Fig. |
A. aspera Pisanty & Wood sp. nov. |
| 35’ | Penis valves parallel-sided or tapering apically, not broadening above visible base (Fig. |
36 |
| 36 (35). | Discs of T1–3 distinctly to obscurely punctate, underlying surface shagreened and dull to partly smooth and shiny. Body length 5–7 mm | 37 |
| 36’ | Discs of T1–2 and often also T3 entirely impunctate, underlying surface shagreened. Body length 4–7 mm | 39 |
| 37 (36). | Penis valves broad basally, occupying almost ½ the space between the gonostyli. Genital capsule with gonocoxites slightly inflated, not smoothly transitioning into gonostyli, base of penis valves slightly bulbous (Fig. |
A. minutuloides Perkins (in part) |
| 37’ | Penis valves narrower basally, occupying <½ the space between the gonostyli (Fig. |
38 |
| 38 (37). | Gonostyli almost parallel-sided, slightly narrowing basally. Penis valves distinctly broader basally vs. apically (Fig. |
A. chananaea Pisanty & Wood sp. nov. (in part) |
| 38’ | Gonostyli with inner margin more strongly narrowing basally. Penis valves more uniformly narrow (Fig. |
A. alfkenelloides cardalia Warncke (in part) |
| 39 (36). | Penis valves very broad basally, uniformly tapering all the way to needle-like apex, therefore shaped as a very elongated triangle (Fig. |
A. tiaretta Warncke |
| 39’ | Penis valves different, either narrower basally and/or not uniformly tapering apically and/or not needle-like apically (Fig. |
40 |
| 40 (39). | Clypeus completely smooth at least in apical half. Body length 4–5.5 mm | 41 |
| 40’ | Clypeus weakly to strongly shagreened apically. Body length 4–7 mm | 42 |
| 41 (40). | Penis valves relatively broad basally. Gonocoxites often slightly rounded apically (Fig. |
A. tringa Warncke |
| 41’ | Penis valves narrower basally. Gonocoxites apically truncate (Fig. |
A. aphroditae Pisanty sp. nov. |
| 42 (40). | T1–3 marginal zones mostly smooth. Penis valves broad basally, occupying almost ½ the space between the gonostyli. Genital capsule with gonocoxites slightly inflated, not smoothly transitioning into gonostyli, base of penis valves slightly bulbous (Fig. |
A. minutuloides Perkins (in part) |
| 42’ | T1–3 marginal zones mostly shagreened. Penis valves narrower basally (Fig. |
43 |
| 43 (42). | Outer margins of gonostyli converging apically, with slight inward kink at mid-length (Fig. |
A. hebraica Pisanty & Wood sp. nov. |
| 43’ | Outer margins of gonostyli uniformly arched, without inward kink (Fig. |
A. paganettina Warncke |
Andrena (Micrandrena) males, terga 2–3 (A, B), vertices (C), genitalia (D–V) and eighth sterna (W). A, M A. libanica; B, N A. lindbergella; C, T A. magunta; D A. yelkouan; E A. extenuata; F, W A. tkalcui; G A. sulfurea; H A. calandra; I A. convexifrons; J A. spreta; K A. friedmani; L A. alshaykh; O A. cervina; P A. phoenicia; Q A. stolida; R A. rugothorace; S A. lunaris; U A. enslinella; V A. luscinia.
See
Andrena dargia
Warncke, 1965: 65–66, ♀ [Greece:
Material of Andrena chananaea sp. nov. from Lebanon was confused with A. minutula (
HOLOTYPE (A. dargia Warncke): GREECE ● 1♀; Delphi; 11 Apr. 1963; Kl. Warncke leg.;
This North African species was mentioned from the West Bank by Alfken (1935), but the material was reidentified as A. iliaca by
As material reported from Lebanon by
TURKEY ● 2♀; Osmania [Osmaniye], Küllü; 1640 m a.s.l.; 9 Jun. 2006; M. Kafka leg.; BOLD accession nos. ANDGP014-25, ANDGP022-25;
GREECE ● 1♀; Lampeia; 30 May 2023; S. Flaminio leg.; BOLD accession no. WPATW1456-23; TJWC. – SPAIN ● 1♀; Balaguer, Camarasa, Aiguabarreig Segre-Noguera Pallaresa; 41.8758° N 0.8508° E; 11 May 2021; T. Wood leg.; BOLD accession no. WPATW108-21; TJWC ● 1♀; Madrona, 500 m NE, Arroyo del Hocino; 40.9006° N –4.1559° W; 15 May 2021; T. Wood leg.; BOLD accession no. WPATW157-21; TJWC.
ISRAEL ● 1♀; Yiftach; 21 Apr. 2015; O. Winberger leg.; pan trap; BOLD accession no. ANDIL173-22; SMNHTAU 184687.
First record from the West Bank.
ISRAEL ● 1♂; Har Hermon; 33.2994° N 35.7675° E; 1645 m a.s.l.; sweeping; 16 Apr. 2021; G. Pisanty leg.; BOLD accession no. ANDIL126-22; SMNHTAU 361398 ● 1♀; Sasa; 20 Apr. 2015; O. Winberger leg.; pan trap; BOLD accession no. ANDIL042-22; SMNHTAU 184788. – WEST BANK ● 4♀; Itamar, 5kmE, ThreeSeas’ Lookout; 860 m a.s.l.; 5 Mar. 2021; L. Friedman leg.; SMNHTAU 357699, 357700, 357705, 357706 ● 1♂; ibid.; SMNHTAU 357703 ● 1♀; ibid.; BOLD accession no. ANDIL491-25; SMNHTAU 357698.
Andrena (Micrandrena) spreta ssp. povolnyi
Warncke, 1974c: 167, ♀♂ [Afghanistan:
Judged by the often subtle morphological differences between A. spreta, A. tiaretta, A. aphroditae sp. nov. and A. hebraica sp. nov., all of which clearly merit species status as supported by molecular barcoding, we believe A. s. povolonyi also differs sufficiently from nominate A. spreta to warrant species status (see also diagnosis section of A. hebraica Pisanty & Wood sp. nov.). The species is currently only known from Afghanistan.
PARATYPES: AFGHANISTAN ● 1♀; O. Afghanistan, Prov. Nengrahar, Darunta; 580 m a.s.l.; 28 Mar. 1967; D. Povolný et coll. leg.;
IRAN ● 1♀; Fars province, Yasuj, Sarb-e Taveh; 2030 m a.s.l.; 4 May 2016; M. Kafka leg.; BOLD accession no. ANDGP020-25;
First record from the Levant.
ISRAEL ● 1♂; Holot Mash’abbim; 30.999° N 34.7578° E; 13 Feb. 2022; G. Pisanty leg.; sweeping, BOLD accession no. ANDIL497-25; SMNHTAU 384336 ● 1♀; ibid.; 18 Feb. 2022; pan trap; BOLD accession no. ANDIL500-25; SMNHTAU 384613.
Conceptualization: GP, TJWC. Data curation: GP, RS, TJWC. Formal analysis: GP, TJWC. Funding acquisition: SC, TJWC. Investigation: GP, RS, TM, TJWC. Methodology: GP, TJWC. Project administration: GP, TJWC. Resources: GP, SC, TJWC. Software: not applicable. Supervision: GP, TJWC. Validation: GP, TJWC. Visualization: GP. Writing – original draft: GP, TJWC. Writing – review & editing: GP, RS, TM, SC, TJWC.
We are grateful to Toshko Ljubomirov (