215 results on '"Pisanty, Gideon"'
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2. Nesting biology, flower preferences, and larval morphology of the little-known Old World bee Ochreriades fasciatus (Apoidea, Megachilidae, Megachilinae)
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Rozen, Jerome G. Jr. (Jerome George), 1928, Pisanty, Gideon, Trunz, Vincent, Bénon, Dimitri, Dorchin, Achik, Praz, Christophe J., American Museum of Natural History Library, Rozen, Jerome G. Jr. (Jerome George), 1928, Pisanty, Gideon, Trunz, Vincent, Bénon, Dimitri, Dorchin, Achik, and Praz, Christophe J.
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Bees ,Behavior ,Host plants ,Insects ,Israel ,Lamiaceae ,Larvae ,Megachilidae ,Nests ,Ochreriades fasciatus ,Phylogeny - Published
- 2015
3. Corrigendum: Delivery of crop pollination services is an insufficient argument for wild pollinator conservation.
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Kleijn, David, Winfree, Rachael, Bartomeus, Ignasi, Carvalheiro, Luísa G, Henry, Mickaël, Isaacs, Rufus, Klein, Alexandra-Maria, Kremen, Claire, M'Gonigle, Leithen K, Rader, Romina, Ricketts, Taylor H, Williams, Neal M, Adamson, Nancy Lee, Ascher, John S, Báldi, András, Batáry, Péter, Benjamin, Faye, Biesmeijer, Jacobus C, Blitzer, Eleanor J, Bommarco, Riccardo, Brand, Mariëtte R, Bretagnolle, Vincent, Button, Lindsey, Cariveau, Daniel P, Chifflet, Rémy, Colville, Jonathan F, Danforth, Bryan N, Elle, Elizabeth, Garratt, Michael PD, Herzog, Felix, Holzschuh, Andrea, Howlett, Brad G, Jauker, Frank, Jha, Shalene, Knop, Eva, Krewenka, Kristin M, Le Féon, Violette, Mandelik, Yael, May, Emily A, Park, Mia G, Pisanty, Gideon, Reemer, Menno, Riedinger, Verena, Rollin, Orianne, Rundlöf, Maj, Sardiñas, Hillary S, Scheper, Jeroen, Sciligo, Amber R, Smith, Henrik G, Steffan-Dewenter, Ingolf, Thorp, Robbin, Tscharntke, Teja, Verhulst, Jort, Viana, Blandina F, Vaissiére, Bernard E, Veldtman, Ruan, Ward, Kimiora L, Westphal, Catrin, and Potts, Simon G
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- 2016
4. Correction: Corrigendum: Delivery of crop pollination services is an insufficient argument for wild pollinator conservation
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Kleijn, David, Winfree, Rachael, Bartomeus, Ignasi, Carvalheiro, Luísa G, Henry, Mickaël, Isaacs, Rufus, Klein, Alexandra-Maria, Kremen, Claire, M’Gonigle, Leithen K, Rader, Romina, Ricketts, Taylor H, Williams, Neal M, Adamson, Nancy Lee, Ascher, John S, Báldi, András, Batáry, Péter, Benjamin, Faye, Biesmeijer, Jacobus C, Blitzer, Eleanor J, Bommarco, Riccardo, Brand, Mariëtte R, Bretagnolle, Vincent, Button, Lindsey, Cariveau, Daniel P, Chifflet, Rémy, Colville, Jonathan F, Danforth, Bryan N, Elle, Elizabeth, Garratt, Michael PD, Herzog, Felix, Holzschuh, Andrea, Howlett, Brad G, Jauker, Frank, Jha, Shalene, Knop, Eva, Krewenka, Kristin M, Le Féon, Violette, Mandelik, Yael, May, Emily A, Park, Mia G, Pisanty, Gideon, Reemer, Menno, Riedinger, Verena, Rollin, Orianne, Rundlöf, Maj, Sardiñas, Hillary S, Scheper, Jeroen, Sciligo, Amber R, Smith, Henrik G, Steffan-Dewenter, Ingolf, Thorp, Robbin, Tscharntke, Teja, Verhulst, Jort, Viana, Blandina F, Vaissiére, Bernard E, Veldtman, Ruan, Ward, Kimiora L, Westphal, Catrin, and Potts, Simon G
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Agricultural ,Veterinary and Food Sciences ,Crop and Pasture Production - Abstract
Nature Communications 6: Article number: 7414 (2015); Published: 16 June 2015; Updated: 18 February 2016. The authors inadvertently omitted Kimiora L. Ward, who managed and contributed data, from the author list. This has now been corrected in both the PDF and HTML versions of the Article.
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- 2016
5. Nests, floral preferences, and immatures of the bee Haetosmia vechti (Hymenoptera, Megachilidae, Osmiini) /
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Gotlieb, Ariella, Pisanty, Gideon, Rozen, Jerome G., Jr. (Jerome George), 1928, Müller, Andreas, Biologe, Röder, Gregory, Sedivy, Claudio, Praz, Christophe J., American Museum of Natural History Library, Gotlieb, Ariella, Pisanty, Gideon, Rozen, Jerome G., Jr. (Jerome George), 1928, Müller, Andreas, Biologe, Röder, Gregory, Sedivy, Claudio, and Praz, Christophe J.
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Bees ,Behavior ,Haetosmia ,Haetosmia vechti ,Heliotropium ,Host plants ,Insects ,Israel ,Larvae ,Nests ,Reḥovot - Published
- 2014
6. Delivery of crop pollination services is an insufficient argument for wild pollinator conservation.
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Kleijn, David, Winfree, Rachael, Bartomeus, Ignasi, Carvalheiro, Luísa G, Henry, Mickaël, Isaacs, Rufus, Klein, Alexandra-Maria, Kremen, Claire, M'Gonigle, Leithen K, Rader, Romina, Ricketts, Taylor H, Williams, Neal M, Lee Adamson, Nancy, Ascher, John S, Báldi, András, Batáry, Péter, Benjamin, Faye, Biesmeijer, Jacobus C, Blitzer, Eleanor J, Bommarco, Riccardo, Brand, Mariëtte R, Bretagnolle, Vincent, Button, Lindsey, Cariveau, Daniel P, Chifflet, Rémy, Colville, Jonathan F, Danforth, Bryan N, Elle, Elizabeth, Garratt, Michael PD, Herzog, Felix, Holzschuh, Andrea, Howlett, Brad G, Jauker, Frank, Jha, Shalene, Knop, Eva, Krewenka, Kristin M, Le Féon, Violette, Mandelik, Yael, May, Emily A, Park, Mia G, Pisanty, Gideon, Reemer, Menno, Riedinger, Verena, Rollin, Orianne, Rundlöf, Maj, Sardiñas, Hillary S, Scheper, Jeroen, Sciligo, Amber R, Smith, Henrik G, Steffan-Dewenter, Ingolf, Thorp, Robbin, Tscharntke, Teja, Verhulst, Jort, Viana, Blandina F, Vaissière, Bernard E, Veldtman, Ruan, Ward, Kimiora L, Westphal, Catrin, and Potts, Simon G
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Animals ,Bees ,Crops ,Agricultural ,Conservation of Natural Resources ,Biodiversity ,Pollination ,Crops ,Agricultural - Abstract
There is compelling evidence that more diverse ecosystems deliver greater benefits to people, and these ecosystem services have become a key argument for biodiversity conservation. However, it is unclear how much biodiversity is needed to deliver ecosystem services in a cost-effective way. Here we show that, while the contribution of wild bees to crop production is significant, service delivery is restricted to a limited subset of all known bee species. Across crops, years and biogeographical regions, crop-visiting wild bee communities are dominated by a small number of common species, and threatened species are rarely observed on crops. Dominant crop pollinators persist under agricultural expansion and many are easily enhanced by simple conservation measures, suggesting that cost-effective management strategies to promote crop pollination should target a different set of species than management strategies to promote threatened bees. Conserving the biological diversity of bees therefore requires more than just ecosystem-service-based arguments.
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- 2015
7. A new species of mining bee (Hymenoptera: Andrenidae: Andrena ) from Israel’s coastal plain
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Pisanty, Gideon, primary, Levy, Karmit, additional, Martin, Teresa, additional, Mandelik, Yael, additional, and Cardinal, Sophie, additional
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- 2023
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8. Wild Pollinators Enhance Fruit Set of Crops Regardless of Honey Bee Abundance
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Garibaldi, Lucas A, Steffan-Dewenter, Ingolf, Winfree, Rachael, Aizen, Marcelo A, Bommarco, Riccardo, Cunningham, Saul A, Kremen, Claire, Carvalheiro, Luísa G, Harder, Lawrence D, Afik, Ohad, Bartomeus, Ignasi, Benjamin, Faye, Boreux, Virginie, Cariveau, Daniel, Chacoff, Natacha P, Dudenhöffer, Jan H, Freitas, Breno M, Ghazoul, Jaboury, Greenleaf, Sarah, Hipólito, Juliana, Holzschuh, Andrea, Howlett, Brad, Isaacs, Rufus, Javorek, Steven K, Kennedy, Christina M, Krewenka, Kristin M, Krishnan, Smitha, Mandelik, Yael, Mayfield, Margaret M, Motzke, Iris, Munyuli, Theodore, Nault, Brian A, Otieno, Mark, Petersen, Jessica, Pisanty, Gideon, Potts, Simon G, Rader, Romina, Ricketts, Taylor H, Rundlöf, Seymour, Colleen L, Schüepp, Christof, Szentgyörgyi, Hajnalka, Taki, Hisatomo, Tscharntke, Teja, Vergara, Carlos H, Viana, Blandina F, Wanger, Thomas C, Westphal, Catrin, Williams, Neal, and Klein, Alexandra M
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Agricultural ,Veterinary and Food Sciences ,Zoology ,Crop and Pasture Production ,Biological Sciences ,Animals ,Bees ,Crops ,Agricultural ,Flowers ,Fruit ,Insecta ,Pollination ,General Science & Technology - Abstract
The diversity and abundance of wild insect pollinators have declined in many agricultural landscapes. Whether such declines reduce crop yields, or are mitigated by managed pollinators such as honey bees, is unclear. We found universally positive associations of fruit set with flower visitation by wild insects in 41 crop systems worldwide. In contrast, fruit set increased significantly with flower visitation by honey bees in only 14% of the systems surveyed. Overall, wild insects pollinated crops more effectively; an increase in wild insect visitation enhanced fruit set by twice as much as an equivalent increase in honey bee visitation. Visitation by wild insects and honey bees promoted fruit set independently, so pollination by managed honey bees supplemented, rather than substituted for, pollination by wild insects. Our results suggest that new practices for integrated management of both honey bees and diverse wild insect assemblages will enhance global crop yields.
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- 2013
9. Watermelon pollinators exhibit complementarity in both visitation rate and single-visit pollination efficiency
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Pisanty, Gideon, Afik, Ohad, Wajnberg, Eric, and Mandelik, Yael
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- 2016
10. Non-bee insects are important contributors to global crop pollination
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Rader, Romina, Bartomeus, Ignasi, Garibaldi, Lucas A., Garratt, Michael P. D., Howlett, Brad G., Winfree, Rachael, Cunningham, Saul A., Mayfield, Margaret M., Arthur, Anthony D., Andersson, Georg K. S., Bommarco, Riccardo, Brittain, Claire, Carvalheiro, Luísa G., Chacoff, Natacha P., Entling, Martin H., Foully, Benjamin, Freitas, Breno M., Gemmill-Herren, Barbara, Ghazoul, Jaboury, Griffin, Sean R., Gross, Caroline L., Herbertsson, Lina, Herzog, Felix, Hipólito, Juliana, Jaggar, Sue, Jauker, Frank, Klein, Alexandra-Maria, Kleijn, David, Krishnan, Smitha, Lemos, Camila Q., Lindström, Sandra A. M., Mandelik, Yael, Monteiro, Victor M., Nelson, Warrick, Nilsson, Lovisa, Pattemore, David E., de O. Pereira, Natália, Pisanty, Gideon, Potts, Simon G., Reemer, Menno, Rundlöf, Maj, Sheffield, Cory S., Scheper, Jeroen, Schüepp, Christof, Smith, Henrik G., Stanley, Dara A., Stout, Jane C., Szentgyörgyi, Hajnalka, Taki, Hisatomo, Vergara, Carlos H., Viana, Blandina F., and Woyciechowski, Michal
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- 2016
11. Profiling crop pollinators: life history traits predict habitat use and crop visitation by Mediterranean wild bees
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Pisanty, Gideon and Mandelik, Yael
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- 2015
12. Andrena (incertae sedis) sulfurea Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (incertae sedis) sulfurea Wood sp. nov. (Figs. 242–250) Female (Fig. 242). Body length: 8–8.5 mm. Colour. Body black (Fig. 242). Flagellum black basally, becoming orange from segment 2 onwards, particularly ventrally (Fig. 243). Apical parts of basitarsi and tarsal segments orange brown. Wings hyaline, stigma and venation orange (Fig. 242). Tergal margins apically lightened translucent orange-yellow (Fig. 245). Pubescence. Face, gena, vertex and scape with dense white hairs of moderate length, none substantially exceeding half of length of scape (Figs. 242–243). Clypeus apically, mandibles and labrum with short golden hairs (Fig. 243). Fovea with short white hairs. Mesonotum and scutellum with semi-squamous whitish-yellowish hairs, very short dorsally, longer anterolaterally (Figs. 242, 244). Mesepisternum with long white hairs. Propodeal corbicula complete, surface of corbicula with sparse, long white simple hairs. Leg hair white, scopal hairs white, simple (Fig. 242). Flocculus complete, short, composed of white plumose hairs. Tergal discs with very short white hairs visible in lateral view, margin of disc 1 laterally with small white hair tuft, 2–4 with complete or only slightly interrupted thick white hairbands that obscure underlying surface. Prepygidial fimbria whitish, pygidial fimbria golden (Fig. 245). Head (Figs. 243–244). 1.3 times broader than long. Labral process narrow, slightly longer than wide. Clypeus very weakly domed, shagreened, dull, densely punctate, punctures separated by 0.5–1 puncture diameters (Fig. 243). Paraocular area and frons finely longitudinally ridged, dull. Flagellomere 1 as long as 2+3. Facial fovea dorsally occupying half distance between lateral ocellus and compound eye, very slightly narrowed below, essentially parallel-sided (Fig. 243). Fovea dorsally separated from lateral ocellus by 1.5 diameter of lateral ocellus. Ocelloccipital distance subequal to width of lateral ocellus. Genal area slightly exceeding width of compound eye (Fig. 244). Mesosoma (Fig. 244). Pronotum without elevated dorsolateral angle or lateral carina. Mesonotum and scutellum smooth and shiny, almost without shagreen, densely punctured, punctures separated by 0.5–1 puncture diameters (Fig. 244). Mesepisternum and propodeal corbicula finely reticulate, impunctate, weakly shining. Propodeal triangle wide, inner surface finely reticulate with delicate pattern of fine raised carinae, laterally delineated by fine carina; posterolateral part of propodeum with similar structure. Inner side of hind femur rounded, not carinate. Tarsal claws with small inner tooth. Recurrent vein 1 reaching submarginal cell 2 at its middle. Submarginal crossvein 1 meets marginal cell 2 vein widths from stigma. Nervulus slightly antefurcal (Fig. 242). Metasoma (Fig. 245). Tergal discs densely and evenly shagreened, weakly shining. Marginal zones slightly depressed, structurally identical, occupying 0.3 of tergal length. Pygidial plate flat, rounded triangular. Male (Fig. 246). Body length: 6.5–7 mm. Colour. Similar to female, though antennae darker brown, never becoming orange, pubescence more obviously white, never whitish-yellow (Fig. 246). Pubescence. Hairs of head as in female, though longer, longest equaling length of scape (Figs. 246–248). Mesonotum and scutellum without semi-squamous hairs, hairs long, longest equaling length of scape (Figs. 246, 248). Terga with hair bands composed of longer hairs, covering margins of terga 2–5 and extending onto following terga by same distance again (Fig. 249). Head (Figs. 247–248). As in female, though with labral process apically with strong emargination, flagellomere 1 exceeds 2, shorter than 2+3. Mesosoma (Fig. 248). As in female, except nervulus slightly less clearly antefurcal (Fig. 246). Tarsal claws more obviously bidentate, with comparatively larger inner tooth. Metasoma (Fig. 249). As in female, but with dense punctures on tergal discs in shagreenation, punctures separated by 0.5–1 puncture diameters, not extending onto tergal margins. Genitalia and hidden sterna (Fig. 250). Gonocoxites produced into strong, blunt and apically rounded dorsal lobes. Gonostyli with raised internal margin, apically spatulate. Penis valves basally broad, apically narrowing abruptly to point (Fig. 250). Sternum 8 narrow, columnar, essentially parallel-sided throughout, apically truncate. Diagnosis. Placement of A. sulfurea into a subgenus is difficult and cannot currently be done with confidence. In the female sex, the species is very close to A. (Graecandrena) schwarzi Warncke because of the small body size, propodeal triangle finely and delicately marked with raised reticulation, nervulus slightly antefurcal, dark integument throughout, strongly shagreened terga with thick, white apical hairbands, and shiny and densely punctured mesonotum and scutellum. However, A. schwarzi is placed into the Graecandrena on the basis of its male genitalia that are typical for this subgenus (see illustrations in Warncke 1975); the genitalia of A. sulfurea are completely different and resemble members of the former subgenus Poliandrena sensu Warncke which no longer exists and most members of which are incertae sedis (Pisanty et al. 2022), specifically the taxa A. castanea Warncke, A. hibernica Warncke, and A. melanota Warncke. Andrena sulfurea females can be separated from A. schwarzi by the dense punctures of the clypeus which are separated by A. schwarzi punctures separated by at least 1 puncture diameter, by>2 centrally, underlying surface smooth and polished, shining), by the presence of semi-squamiform hairs on the mesonotum (mesonotal hairs longer, of a normal type in A. schwarzi), and by the shape of the labral process which is narrow, slightly longer than wide (labral process trapezoidal, approximately twice as wide as long in A. schwarzi). It is superficially similar to certain members of the Andrena aerinifrons species group (Carandrena sensu Warncke, now included in Notandrena, Pisanty et al. 2022) which lack metallic reflections such as A. pesleria Gusenleitner, but can be separated by the reticulate propodeal triangle (smooth in comparative aerinifrons -group species). It can also be separated from the group of aforementioned ‘ Poliandrena ’ species by the absence of tergal punctures; all three taxa have clearly punctured terga. Andrena sulfurea males can be separated from the three mentioned ‘ Poliandrena ’ species by the black clypeus, thick and long white tergal hairbands, white facial hairs, and penis valves which narrow abruptly apically (narrow more slowly, remaining comparatively wide throughout in the ‘ Poliandrena ’ species) (Figs. 250–253). Distribution: Central Syria. Flight period: March, presumably into April. Flower records: None. Holotype: SYRIA: Homs, 250 m, As Sukhnah [As-Shuknah], 22 km E, 24.iii.1988, L. Blank, ♂ (OLML). Paratypes: SYRIA: Homs, 250 m, As Sukhnah [As-Shuknah], 22 km E, 24.iii.1988, L. Blank (2♀, 14♂); 80 km E of Palmyra, 450 m, 22.iv.1992, K. Warncke (19♀, 8♂); 110 km E of Palmyra, 350 m, 21–22.iv.1992, K. Warncke (1♂) (OLML, SMNHTAU, TJW). Etymology. sulfurea = Latin for “sulphurous”, in reference to the type locality’s nearby sulfur springs that also give As Sukhnah its name (literally ‘the warm’ in Arabic). The species epithet is an adjective. Other material examined: (A. castanea): PARATYPE: TURKEY: Karadağ, Karaman Province [Karadagh], 1.vi.1920, (1♂) (OLML); (A. hibernica caucasica) : HOLOTYPE: CAUCASUS: Arexesthal (unknown location, Arexes = Aras river, flows from Turkey to the Caspian Sea), 1889 [89], Reitter (♂) (OLML); (A. melanota): PARATYPE: TURKEY: Erzurum, 31.viii.1937, O. Ecevit [sic?] (1♂) (OLML)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 97-100, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Warncke, K. (1975) Die Sandbienen der Turkei (Hymenoptera, Apoidea, Andrena), Teil B. Beschreibungen der neuen Andrena - Arten bzw. Unterarten. Mitteilungen der Munchner Entomologischen Gesellschaft, 65, 29 - 102.","Pisanty, G., Richter, R., Martin, T., Dettman, J. & Cardinal, S. (2022) Molecular phylogeny, historical biogeography and revised classifcation of andrenine bees (Hymenoptera: Andrenidae). Molecular Phylogenetics and Evolution, 170, 107151."]}
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- 2022
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13. Andrena (Micrandrena) rubecula Warncke 1974
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Andrena rubecula ,Taxonomy - Abstract
Andrena (Micrandrena) rubecula Warncke, 1974 Distribution: Egypt, Libya (Gusenleitner & Schwarz 2002). Likely present in southern Israel. Flight period: February–April (Warncke 1974a). Flower records: None. Material examined: HOLOTYPE: EGYPT: Cairo, Maadi [Meadi], 20.ii.1931, H. Priesner (♀) (OLML); PARATYPE: EGYPT: Wadi Digla, 13.iii.1931, Dr. H. Priesner (1♀) (SMNHTAU); non-type material : EGYPT [ISRAEL]: Taba, 19.iii.1988, Y. Zvik (2♀) (SMNHTAU). Remarks. The collecting locality of Taba is only about 1 km from the Israeli border, and the species is therefore likely to occur also in Israel., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 59, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Gusenleitner, F. & Schwarz, M. (2002) Weltweite Checkliste der Bienengattung Andrena mit Bemerkungen und Erganzungen zu palaarktischen Arten (Hymenoptera, Apidae, Andreninae, Andrena). Entomofauna, Supplement 10, 1 - 1280.","Warncke, K. (1974 a) Beitrag zur Kenntnis und Verbreitung der Sandbienen in Nordafrika (Hymenoptera, Apoidea, Andrena). Mitteilungen aus dem Zoologischen Museum in Berlin, 50, 2 - 53."]}
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- 2022
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14. Andrena (incertae sedis) hulae Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (incertae sedis) hulae Pisanty sp. nov. (Figs. 210–213) Female (Fig. 210). Body length: 8.5 mm. Colour. Head and mesosoma dark brown to black (Figs. 210–212). Anterior side of flagellomeres 3–10 orange. Legs and metasoma brown (Figs. 210, 213). Last tarsal segment orange. Wings hyaline, veins brown, stigma dark orange to brown (Fig. 210). Tergal marginal zones reddish basally, yellowish apically (Fig. 213). Pubescence. Clypeus with short and thin whitish hair. Paraocular area with medium-lengthed white hair. Scape with short white hair. Frons with short white hair. Foveae with short whitish hair. Vertex with medium yellowishwhite hair (Figs. 211–212). Genal area with short to medium white hair. Mesonotum, scutellum and metanotum with short to medium yellowish-white hair, mostly on periphery (Figs. 210, 212). Mesepisternum with long white hair. Propodeal corbicula incomplete, posterodorsal fringe with long white plumose hairs, corbicular surface with medium to long white plumose hairs. Leg hair white to golden. Flocculus complete, white. Tibial scopal hairs simple, white (Fig. 210). Tergal discs almost hairless medially, laterally with short whitish hairs. Tergal marginal zones 2–4 with broadly interrupted bands of white hair. Terminal fringe golden (Fig. 213). Head (Figs. 211–212). 1.2 times broader than long. Galea shagreened, matt. Labral process smooth, much broader than long, apical margin slightly arched. Clypeus moderately protuberant, strongly arched, basal half strongly and finely shagreened, apical half gradually smooth, punctation fine and dense, distance between punctures 1–1.5 puncture diameters (Fig. 211). Malar area length 0.2 times width of mandible base. Flagellomere 1 longer than 2+3. Frons longitudinally striated, interspersed with sparse, shallow fine punctures. Facial foveae broad, occupying slightly more than half distance between compound eye and lateral ocellus (Figs. 211–212). Distance of fovea from lateral ocellus 1.5 times width of lateral ocellus. Ocelloccipital distance 1.4 ocellus diameters. Vertex carinate. Genal area 1.2 times as broad as compound eye (Fig. 212). Mesosoma (Fig. 212). Dorsolateral angle of pronotum not elevated, pronotum not carinate. Mesonotum strongly and uniformly shagreened, weakly shiny, with dense, shallow but distinct, coarse crater-like punctures, distance between punctures 0.5–1 puncture diameters. Scutellum shagreened peripherally, shiny and weakly shagreened centrally, with regular (not crater-like) punctures, distance between punctures 1 puncture diameter (Fig. 212). Mesepisternum finely alveolate, densely and shallowly punctured, punctures merging onto underlying sculpture. Propodeal corbicula finely reticulate. Posterior part of propodeum clearly divided into basal, moderately sloping part, and apical vertical part. Posterolateral part of propodeum finely alveolate, shallowly, obliquely punctured. Propodeal triangle narrow, rugose basally, finely alveolate apically. Inner side of hind femur not carinate. Inner hind tibial spur almost straight, of uniform width. Hind pretarsal claw bidentate. Nervulus interstitial (Fig. 210). Submarginal crossvein 1 meets marginal cell 4 vein widths from stigma. Metasoma (Fig. 213). Tergal discs impunctate, 1–2 finely shagreened, 3–4 weakly, finely shagreened and shiny. Tergal marginal zones similarly sculptured, smooth near apex, 2–4 slightly depressed, centrally occupying 1/3–1/2 of tergum length. Pygidial plate finely alveolate, rounded apically, without elevated central area. Male. Unknown. Diagnosis. Andrena hulae is most similar to A. ramosa Wood, recently described from southern Spain, which is morphologically related to the subgenus Planiandrena (Wood et al. 2022). However, recent molecular findings show that the COI barcode of A. ramosa falls closest to species of Euandrena, questioning its subgeneric placement (TJW, unpublished results). We therefore place both A. hulae and A. ramosa as incertae sedis for the time being. Andrena hulae is similar to Planiandrena species in its short and broad labral process and its relatively broad propodeal triangle with short longitudinal rugae basally, but its fovea is substantially broader, the hind tibial spur is not broadened submedially, and the pygidial plate lacks a centrally elevated area. Compared to A. ramosa, A. hulae can be separated by its smaller body size of 8.5 mm (12 mm in A. ramosa), its broad foveae that occupy over half the space between the compound eye and the lateral ocellus (occupying 1/3 of this space, separated from lateral ocellus by over two times diameter of lateral ocellus in A. ramosa), propodeal triangle with short basal longitudinal rugae (without rugae basally in A. ramosa), its flat and centrally alveolate pygidial plate (pygidial plate with smooth surface, with weakly raised longitudinal ridge in A. ramosa), and by its weakly plumose hairs on the mesepisternum, propodeal corbiculae, flocculus, and femoral scopae (these areas with extremely long and extremely plumose hairs in A. ramosa). Distribution: Northern Israel. Flight period: March. Flower records: None. Holotype: ISRAEL: Sde Eliezer [Sede Eli’ezer], N Rosh-Pina, 19.iii.1995, R. Kasher, ♀ (SMNHTAU:367741). Paratypes: ISRAEL: same as holotype (1♀) (SMNHTAU). Etymology. Named after the Hula Valley in northern Israel, where the species was collected. The species epithet is an adjective., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 87-88, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Wood, T. J., Molina, F. P. & Bartomeus, I. (2022) A new Andrena species (Hymenoptera: Andrenidae) from the overlooked Donana Protected Areas of southern Spain. Belgian Journal of Entomology, 126, 1 - 13. https: // doi. org / 10.47446 / OSMIA 10.1"]}
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- 2022
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15. Andrena (Poecilandrena) veronicae Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Andrena veronicae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Poecilandrena) veronicae Pisanty & Wood sp. nov. (Figs. 148–152, 155–159, 161) Female (Fig. 148). Body length: 7.5–8 mm. Colour. Basal half of clypeus with rainbow-like pattern of alternating green, yellow, red, purple and blue metallic hues; apical half black. Face above clypeus and genal area with golden, green and/or blue metallic luster (Fig. 149). Anterior side of flagellomeres 5–10 orange (Fig. 148). Pronotum, mesonotum, scutellum and metanotum with blue to golden metallic luster (Fig. 150). Mesepisternum and propodeal corbicula dark, often with weak bluish metallic luster. Posterior part of propodeum black (Fig. 150). Legs dark brown. Wings slightly infuscate, veins and stigma dark brown (Fig. 148). Tergal discs with weak to strong metallic luster, mostly bluish, sometimes weakly golden. Tergal marginal zones reddish-brown basally, golden apically (Fig. 151). Pubescence. Body hair mostly golden to light brown, moderately plumose (Fig. 148). Clypeus with moderately dense short hairs, mostly golden, on apical half intermixed with black hairs. Frons, scape and paraocular area with moderately dense, medium-lengthed golden hairs and few short black hairs (Fig. 149). Facial foveae brown in dorsal view (Fig. 150). Vertex with short to long golden hair. Genal area with short to medium golden hair, slightly brighter ventrally. Mesonotum with short, thin, erect golden hairs, denser and thicker peripherally. Metanotum and lateral margins of scutellum with dense, medium-lengthed, erect, whitish to golden hair. Mesepisternum with long hair, golden dorsally, whitish medially and ventrally. Propodeal corbicula incomplete, dorsoposterior fringe with long, whitish-golden plumose hairs, corbicular surface with minute hairs and few long, whitish-golden, weakly plumose hairs. Legs with golden to yellowish hair; flocculus complete, yellowish; scopal hairs simple, golden (Fig. 148). Terga with golden hairs, minute medially, short laterally, denser on marginal zone 4. Tergal apical hair bands not developed. Prepygidial fimbria golden to light brown; pygidial fimbria dark brown (Fig. 151). Head (Figs. 149–150). 1.2 times broader than long. Mandible bidentate. Galea shallowly and finely shagreened. Labral process broad, trapezoidal, basal margin transversely striated, otherwise mostly smooth, apical margin blunt to slightly emarginate. Clypeus convex, shagreened, moderately punctured, distance between punctures 0.5–2 puncture diameters (Fig. 149). Flagellomere 1 slightly shorter than 2+3+4, 2–4 more or less the same length. Frons and upper half of paraocular area longitudinally striated, distinctly punctured, area under medial ocellus more finely striated and densely and finely punctured. Facial foveae relatively short, of moderate, uniform width, extending from level of middle–lower end of medial ocellus to slightly below antennal socket, 0.4 times as broad as antennocular distance (Figs. 149–150). Distance of fovea from lateral ocellus about 2 ocellus diameters. Ocelloccipital distance 1.2 ocellus diameters. Vertex weakly carinate (Fig. 150). Mesosoma (Figs. 150, 152). Dorsolateral angle of pronotum not to very slightly elevated, lateral carina absent. Mesonotum strongly shiny, smooth to very superficially shagreened, finely punctured, distance between punctures 0.5–2 puncture diameters. Scutellum similar, more strongly shagreened (Figs. 150, 152). Mesepisternum and propodeal corbicula finely reticulate, anterior part of mesepisternum shallowly, obliquely punctured. Posterolateral part of propodeum finely and shallowly alveolate, shallowly, obliquely punctured. Propodeal triangle weakly delineated by shallow carina, basal margin radially rugose, apical part gradually finely alveolate. Inner side of hind femur not significantly carinate. Hind pretarsal claw bidentate. Recurrent vein 1 meeting submarginal cell 2 at its middle or slightly distal to it. Nervulus interstitial to very slightly postfurcal (Fig. 148). Metasoma (Fig. 151). Tergal discs shiny, smooth to weakly and very finely shagreened, finely punctured, distance between punctures 0.5–1 puncture diameters; vertical part of tergum 1 very shallowly shagreened, very sparsely and finely punctured. Tergal marginal zones narrow, weakly arched, weakly depressed, weakly and finely shagreened, very finely punctured, distance between punctures about 1 puncture diameter. Pygidial plate with raised margin, without elevated medial zone, apical margin blunt to weakly truncate. Male (Fig. 155). Body length: 6.5–7 mm. Colour. Head dark, with variable degree of bluish-greenish metallic luster (Fig. 156). Clypeus mostly yellow, except for a narrow dark peripheral margin, in some specimens occupying up to 1/4 of clypeus length basally, and occasionally two dark mediolateral spots (Fig. 156). Anterior side of flagellomeres 5–10 mostly orange. Mesonotum, scutellum and metanotum with strong greenish-bluish metallic luster (Fig. 157). Pronotum, mesepisternum and propodeum with weak bluish metallic luster. Legs dark brown to black, apical tarsomeres brown. Wings hyaline, veins and stigma brown (Fig. 155). Tergal discs 1 and 5 black, 2–4 partly to fully orange. Tergal marginal zone 1 black to orange, 2–5 golden (Fig. 158). Pubescence. Head and mesosoma mostly with moderately dense, medium-lengthed white to golden plumose hairs, usually brighter ventrally (Figs. 155–157). Legs with white to light brown hairs, long on ventral side of femora, elsewhere mostly short (Fig. 155). Tergal discs with minute, inconspicuous white hair. Tergal marginal zones 2–4 with very weak, inconspicuous bands of short white to yellowish hairs. Tergal marginal zone 5 and terminal fringe with distinct golden to light brown hairs (Fig. 158). Head (Figs. 156–157). 1.3 times broader than long. Labral process very short and broad, apical margin slightly concave. Clypeus moderately convex, basal half shagreened, apical half smooth, moderately punctured, distance between punctures 1–2 puncture diameters, punctures sparser apically (Fig. 156). Lower part of supraclypeal area obliquely punctured; upper part and frons longitudinally striated with interspersed fine punctures. Flagellomere 1 longer than 2+3, 2 as long as 3 or slightly shorter. Ocelloccipital distance about 1.5 ocellus diameters (Fig. 157). Posterior margin of genal area rounded. Mesosoma (Fig. 157). Dorsolateral angle of pronotum not to slightly elevated, pronotum not carinate. Mesonotum mostly smooth and shiny, anterior margin often shallowly and finely shagreened, punctation moderate, distance between punctures 1–3 puncture diameters. Scutellum finely punctured, anterior half often smooth, posterior half densely punctured (Fig. 157). Propodeal triangle radially rugose basally, finely reticulate to finely rugose apically. Mesepisternum and lateral part of propodeum reticulate, the former with shallow oblique punctures. Metasoma (Fig. 158). Tergal disc 1 superficially shagreened basally and laterally, smooth medioapically, 2–4 mostly smooth, 5 weakly shagreened; tergal disc punctation fine, distinct, distance between punctures 1 puncture diameter. Tergal marginal zones very finely punctured basally, impunctate apically, 1 finely shagreened, 2–4 more or less smooth. Genitalia and hidden sterna (Figs. 159, 161). Dorsal gonocoxite lobes and gonostyli elongate. Penis valves with lateral lamella, creating a spade shape (Figs. 159, 161). Sternum 8 columnar, of uniform width, apical process broadened. Diagnosis. The female of Andrena veronicae is distinguished from most other Poecilandrena by the very shiny, more or less smooth mesonotum and terga. It most closely resembles A. freidbergi Pisanty & Scheuchl, known from high altitudes in Lebanon and Mount Hermon, and A. segregata Osytchnjuk, known from Central Asia. It differs from A. freidbergi in the finer, sparser mesonotal punctation (Figs. 152–153), interstitial nervulus (often weakly postfurcal in A. freidbergi), and medial position of recurrent vein 1 in submarginal cell 2 (more distal in A. freidbergi). Unlike A. semirubra Morawitz, the terga of A. veronicae females are completely dark, without red colouration (Fig. 151). Females of A. semirubra also occasionally occur in a dark tergal form, although they can be distinguished by the denser mesonotal punctures (separated by 0.5–1 puncture diameters) compared to A. veronicae (Figs. 152, 154). The males of A. veronicae are very similar to A. semirubra and have been confused with the latter (Warncke 1969; Pisanty et al. 2018). The male of A. veronicae is larger than that of A. semirubra, and there are subtle differences in the genital capsule: the gonostylus blades are broader and more spatulate, the gonocoxite lobes broader and more rounded, and the lamella of the penis valves extends further apically (Figs. 159–162). Distribution: Northern Israel (Golan Heights), Syria, southwestern Turkey. Likely present also in Lebanon. Flight period: February–May. Flower records: Plantaginaceae: Veronica syriaca. Most specimens were not collected directly from flowers, but V. syriaca was in abundant bloom at the two main collecting locations (Odem Forest and Mount Hermon), and is assumed to be the main host plant, as often seen in the Andrena viridescens species group (Pisanty et al. 2018). Holotype: ISRAEL: Odem Forest Nature Reserve [Ya’ar Odem N.R.], 1.iii.2018, G. Pisanty, ♀ (SMNHTAU:286348). Paratypes: ISRAEL: Mount Hermon [Har Hermon], 1420 m, 33.2855°N 35.763°E, 7.iv.2021, G. Pisanty, pan trap (1♀); 1600 m, 33.300°N 35.767°E, 11.v.2020, G. Pisanty, pan trap (1♀); 1610 m, 33.300°N 35.767°E, 7.iv.2021, G. Pisanty, pan trap (17♀, 16♂); 1640 m, 33.300°N 35.7675°E, 7.iv.2021, G. Pisanty, sweeping (2♀, 5♂); 1642 m, 33.2996°N 35.7677°E, 16.iv.2022, G. Pisanty, pan traps (2♂); 1644 m, 33.2991°N 35.7667°E, 16.iv.2022, G. Pisanty, pan traps (1♀, 7♂); 33.2992°N 35.7670°E, 16.iv.2022, G. Pisanty, pan traps (3♀, 14♂); 1645 m, 33.2994°N 35.7675°E, 16.iv.2021, G. Pisanty, pan traps (7♀, 1♂) and sweeping (2♀); [Hermon], 1500 m, 22.iv.1969, H. Bytinski-Salz (1♂); 1650 m, 20.iv.1969, H. Bytinski-Salz (6♂); [Hermon], Har Shezif, 1447 m, 33.286°N 35.7524°E, 16.iv.2022, G. Pisanty, pan trap (1♀); Odem Forest Nature Reserve [Ya’ar Odem N.R.], 1.iii.2018, G. Pisanty (9♀, 5♂); [Ya’ar Odem NR], 33.186°N 35.7356°E, 27.ii.2020, G. Pisanty, pan traps (1♀, 12♂); 33.206°N 35.736°E, 27.ii.2020, G. Pisanty, on Veronica syriaca (2♂) and from pan traps (2♀, 30♂) and sweeping (1♂); SYRIA: Latakia, Qaranjah, 750 m, 3.iv.1988, M. Schwarz (2♂); TURKEY: Akseki / Taurus, 1300 m, 25.iv.1973, K. Warncke (3♂) (ES, NHMUK, OLML, RMNH, SMNHTAU, TJW, ZMHB, ZSMC). Etymology. From the likely host plant, Veronica syriaca. The species epithet is an adjective. Other material examined (A. semirubra): AZERBAIJAN: Araxesthal, 1890, Reitter (1♀); CRIMEA: Kara Dag [Karadagh], Vodianja balka, Wald, 10.v.2002, Y. Budaschkin (1♀, 4♂); GEORGIA: Tbilisi, 16.v.1978, M. Koucourek (1♀); RUSSIA: Kamyshin [КамЫШИн], 14–19.v.1951, D. Panfilov (2♀); TURKEY: Ağri, 20 km N Patnos, 1650 m, 29.v.1980, K. Warncke (1♀); 20 km N, 1800 m, 28.v.1980, K. Warncke (1♂); Erzurum, 11.v.1971, H. Ozbek (1♀); Erzurum: Ispir, 17.vi.1973, K. Warncke (8♀); Gürün, 1900 m, 12.vi.1973, K. Warncke (2♀, 2♂); Hakkari, pass Suvari Halil, 2500 m, 2.vi.1980, K. Warncke (1♂); Hakkari, 10 km SW Yüksekova, 1780 m, 10.vi.1981, K. Warncke (3♀); Kastamonu, between Tosya and İskilip, 1507 m, 40°56’18’’N 34°15’10’’E, 19.vi.2006, E. Scheuchl (1♀); Mount Nemrut [Nemrut Dagi mt.], 50 km NE of Kanta, 2–14.vi.1996, P. Jelinek (1♀); Şemdinli, 1700 m, 12.vi.1981, K. Warncke (1♀); UluDağ, bei Bursa, 200–1000 m, 15.v–10.vi.1959, Schweiger (2♀) (OLML, SMNHTAU)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 65-69, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Warncke, K. (1969) A contribution to the knowledge of the genus Andrena (Apoidea) in Israel. Israel Journal of Entomology, 4, 377 - 408.","Pisanty, G., Scheuchl, E. & Dorchin, N. (2018) Taxonomic revision of the subgenus Andrena (Poecilandrena) (Hymenoptera: Andrenidae) in Israel and the Levant. Zootaxa, 4374 (2), 151 - 188. https: // doi. org / 10.11646 / zootaxa. 4374.2.1"]}
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16. Andrena (Aciandrena) xera Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Andrena xera ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Aciandrena) xera Pisanty sp. nov. (Figs. 45–49) Female (Fig. 45). Body length: 6.5 mm. Colour. Body black (Fig. 45). Flagellomeres 1–3 brown basally, orange apically; 4–10 orange (Figs. 45–47). Mid and hind femora and basal 3/4 of mid tibia dark brown. Mid and hind tarsi, hind tibia and apical 1/4 of mid tibia golden. Wings hyaline, veins and stigma golden (Fig. 45). Tergal marginal zones reddish-orange basally, yellowish apically (Fig. 49). Pubescence. Body hair mostly sparse, short, minutely plumose, white to yellowish (Fig. 45). Clypeus with sparse short white hair. Lower 2/3 of paraocular area with dense, white medium-lengthed hair. Scape and area between antennal sockets with white to yellowish hair (Fig. 46). Facial foveae dark in ventral view, brownish-white in dorsal view (Figs. 46–47). Vertex with medium-lengthed yellowish-white hair. Genal area with short yellowish-white hair dorsally, medium white hair ventrally. Mesonotum, scutellum and metanotum with relatively thick, yellowish hair, very short and moderately dense medially, short to medium and dense peripherally (Fig. 47). Mesepisternum with long white hair. Propodeal corbicula incomplete, dorsoposterior fringe with long white plumose hair, corbicular surface with few long, white simple hairs. Leg hair mostly white; scopal hairs simple, white (Fig. 45). Tergal discs with short to medium white hair laterally; tergal discs 1–3 hairless medially. Tergal marginal zones with dense, thick bands of white hair, extending to over 1/2 the length of following tergal disc medially, limited to small lateral patches on tergum 1, interrupted on 2, continuous on 3–4. Prepygidial fimbria white laterally, mostly golden medially; pygidial fimbria golden (Fig. 49). Head (Figs. 46–47). 1.2 times broader than long. Galea shiny, superficially shagreened. Labral process narrow, almost square-shaped, apical margin slightly emarginate. Clypeus almost flat, basal half superficially shagreened, apical half smooth, moderately punctured, distance between punctures 1.5–2 puncture diameters, punctation slightly sparser medially, without impunctate midline (Fig. 46). Supraclypeal plate not striated. Flagellomere 1 longer than 2+3, 2 as long as 3. Frons longitudinally striated. Facial fovea broad, weakly tapering downwards, extending from level of middle of lateral ocellus to lower end of antennal socket, 0.5 times as broad as antennocular distance (Fig. 46). Distance of fovea from lateral ocellus 0.7 ocellus diameters. Ocelloccipital distance 1 ocellus diameter. Vertex weakly carinate (Fig. 47). Genal area 0.9 times as broad as compound eye. Mesosoma (Figs. 47–48). Pronotum without elevated dorsolateral angle or lateral carina. Mesonotum finely shagreened on anterior 1/3, smooth medially, punctation very fine, distance between punctures 1–2 puncture diameters (Fig. 47). Scutellum very smooth on anterior 2/3, punctation slightly sparser. Mesepisternum finely alveolate, finely obliquely punctured. Propodeal corbicula finely reticulate. Posterior part of propodeum finely alveolate, triangle weakly delineated from flanking regions, sculptured slightly coarser, with a weak, short mediobasal ruga (Fig. 48). Hind pretarsal claw unidentate. Recurrent vein 1 meets submarginal cell 2 at its middle or slightly distal to it. Submarginal crossvein 1 meets marginal cell 3 vein widths from stigma. Nervulus distinctly antefurcal (Fig. 45). The single available specimen lacks both front legs (removed for DNA extraction), which are therefore absent from the description. Metasoma (Fig. 49). Tergal discs shagreened and impunctate, 1–2 strongly so, 3–4 more superficially, weakly shiny. Tergal marginal zones similarly sculptured, 1–2 not depressed, 3–4 depressed and distinctly arched, medially occupying 1/2 tergum length. Pygidial plate centrally with raised longitudinal ridge. Male. Unknown. Diagnosis: Andrena xera is closest to A. palmyriae Wood and A. pavonia Warncke. All three are desert habitat species with short semi-squamous hairs on the mesonotum and scutellum, orange hind tibiae, and thick white hairbands covering the tergal margins. Andrena xera can be separated by the absence of an impunctate midline on the clypeus (present in A. palmyriae and A. pavonia), medially smooth mesonotum (completely smooth in A. palmyriae, completely shagreened in A. pavonia), weakly notched labral process (deeply notched in A. palmyriae), antefurcal nervulus (more or less interstitial in A. palmyriae), and very broad tergal hair bands (narrower in A. pavonia). Distribution: Israel (Arava valley). Likely present also in Jordan. Flight period: February. Flower records: Brassicaceae. Holotype: ISRAEL: Nahal Shezaf, 30.722ºN 35.270ºE, 14.ii.2016, G. Pisanty, on Brassicaceae, ♀ (SMNHTAU:234067). Etymology. xera = Greek for “dry”, in reference to extreme desert habitat of this species. The species epithet is an adjective., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 26-28, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826
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17. Andrena (Aciandrena) anathema Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Insecta ,Arthropoda ,Andrena anathema ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Aciandrena) anathema Pisanty sp. nov. (Figs. 1–9) Female (Fig. 1). Body length: 5–5.5 mm. Colour. Head, mesosoma and legs dark brown to black; metasoma brown to black (Fig. 1). Anterior side of flagellomeres 3–10 orange (Fig. 2). Wings hyaline, veins brown, stigma brownish-golden (Fig. 1). Tergal marginal zones yellowish-golden apically, often somewhat reddish (Fig. 4). Pubescence. Body hair mostly short and sparse, minutely plumose to plumose, whitish (Fig. 1). Clypeus and supraclypeal area with sparse, short and thin, minutely plumose whitish hair. Paraocular area and scape with moderately dense, short whitish plumose hair (Fig. 2). Facial foveae in dorsal view brownish on upper half, whitish on lower half. Vertex with erect, short yellowish plumose hairs (Fig. 3). Genal area with short whitish, minutely plumose hair. Mesonotum, scutellum and metanotum with short whitish to light brown plumose hair, sparse on center of mesonotum and anterior half of scutellum, dense and thick (semi-squamous) peripherally (Fig. 3). Mesepisternum with medium-lengthed minutely plumose white hair. Propodeal corbicula incomplete, dorsoposterior fringe with long white plumose hair, corbicular surface with few long white simple hairs. Leg hair mostly short, white to light brown (Fig. 1); tibial scopal hair simple, whitish; flocculus incomplete, white. Tergal discs 1–2 hairless, 3–4 with sparse inconspicuous minute whitish hairs. Tergal marginal zones 2–4 with weak bands of short white hair, broadly interrupted on 2–3, continuous but sparser on 4. Terminal fringe golden (Fig. 4). Head (Figs. 2–3). 1.2 times broader than long. Mandible bidentate. Galea shagreened. Labral process more or less triangular. Clypeus flat, shagreened, occasionally with a small smooth medioapical area, shallowly and finely punctured, distance between punctures 2 puncture diameters, without impunctate midline (Fig. 2). Supraclypeal plate finely shagreened, not striated, finely punctured. Flagellomere 1 slightly shorter than 2+3. Frons finely and shallowly longitudinally striated. Facial foveae tapering downwards, extending from level of middle of lateral ocellus to middle of antennal socket, 0.5 times as broad as antennocular distance (Fig. 2). Distance of fovea from lateral ocellus about 1 ocellus diameter. Ocelloccipital distance 0.5 ocellus diameter. Vertex strongly carinate medially (Fig. 3). Mesosoma (Fig. 3). Mesonotum and scutellum shiny, weakly but uniformly shagreened, punctation fine and shallow, distance between punctures 1–3 puncture diameters (Fig. 3). Mesepisternum and propodeum finely reticulate. Propodeal triangle delineated by weak carina, basal part somewhat more coarsely sculptured than flanking areas outside triangle. Hind pretarsal claw unidentate. Recurrent vein 1 meets submarginal cell 2 at its proximal 1/3–1/2. Submarginal crossvein 1 meets marginal cell 1–2 vein widths from stigma (Fig. 1). Nervulus distinctly antefurcal. Metasoma (Fig. 4). Tergal discs shagreened and impunctate. Tergal marginal zones similar, smooth near apex, slightly arched, medially covering 1/3–1/2 of tergum length, 2–4 weakly depressed. Male (Fig. 5). Body length: 4.5 mm. Colour. Similar to female (clypeus and paraocular area dark). Pubescence. Clypeus, paraocular and supraclypeal areas and scape with moderately dense, short to medium white plumose hair (Fig. 6). Genal area with short greyish-white hair anterodorsally, medium white hair posteroventrally. Mesonotum, scutellum and metanotum with sparse, short to long, white to yellowish minutely plumose hair (Fig. 7). Mesepisternum and propodeum with long plumose white hair. Femora and tibiae mostly with short white to yellowish hair. Tarsi with short white to golden hair (Fig. 5). Tergal discs 2–4 and basal half of 1 with minute inconspicuous white hairs, apical half of 1 almost hairless. Apical half of tergal marginal zones 2–4 with weak, strongly interrupted bands of short white to whitish-golden hairs. Tergal marginal zone 5 with sparse band of medium-lengthed whitish-golden hairs. Terminal fringe whitish-golden (Fig. 5). Head (Figs. 6–7). Labral process weakly trapezoidal, slightly broader than long, very finely transversely striated, apical margin concave. Clypeus not to weakly protuberant at apical half, flattened, shiny, basal half shagreened, apical half shagreened to smooth, punctation moderate, distance between punctures 1.5–3 puncture diameters, without impunctate midline (Fig. 6). Flagellomere 1 shorter than 2+3, 2 slightly shorter than 3. Rest of head similar to female. Mesosoma (Fig. 7). Basal part of propodeal triangle finely alveolate, more strongly sculpted than in female. Hind pretarsal claw bidentate. Otherwise similar to female. Metasoma. Similar to female. Genitalia and hidden sterna (Figs. 8–9). Dorsal gonocoxite lobes developed, broadly rounded. Gonostylus broadening at 1/3 of its length, blade flattened, of uniform width, apical margin more or less rounded. Penis valves moderately broad basally, gradually tapering towards narrow apex (Fig. 8). Sternum 8 simple, columnar, apical process broadened, blunt-ended (Fig. 9). Diagnosis. Andrena anathema and the closely related A. (Aciandrena) longistilus sp. nov. are distinguished from most other Aciandrena by the distinctly flattened clypeus (Figs. 2, 6, 19, 23). As far as we can see, the females of the two species cannot be morphologically differentiated, and were hereby assigned to species based on DNA barcoding (Table 2). Moreover, preliminary molecular data suggests that there may be additional, undescribed Levantine species of very similar morphology (GP, unpublished results). Use of DNA barcoding is therefore essential for validating specimen identity and establishing species boundaries within this difficult taxonomic group. Females of A. anathema and A. longistilus resemble those of A. (Aciandrena) spolata Warncke, but in the latter species the clypeus is flattened to a lesser extent, very slightly convex, and always smooth apically (usually with majority of surface area shagreened in A. anathema and A. longistilus). Additionally, A. spolata has a narrowly trapezoidal labral process (more triangular in A. anathema and A. longistilus) and stronger mesonotal punctation. Andrena (Graecandrena) impunctata Pérez possesses a similarly flattened clypeus, but has a larger body size, broadly trapezoidal labral process (triangular in A. anathema and A. longistilus), striated supraclypeal plate, and narrower facial foveae. The male of A. anathema closely resembles A. (Aciandrena) israelica Scheuchl & Pisanty and was confused with the latter species, with representatives included in its type series (Pisanty et al. 2016). Compared to A. israelica, the clypeus and mesonotum of A. anathema are without metallic luster and more distinctly punctured, the clypeus is flattened and often smooth apically (slightly convex and fully shagreened in A. israelica), flagellomeres 2–11 are reddish to orange (light brown in A. israelica), the nervulus is more weakly antefurcal, and the terga are more strongly shagreened. The genital capsules of the two species are almost identical; in direct comparison, the dorsal gonocoxite lobe and the base of the gonostylus of A. israelica seem slightly broader. Distribution: North and central Israel, West Bank, reaching south as far as 31.4°N. Seems to exhibit a vicariance pattern with A. longistilus sp. nov., which occupies drier habitats located further south or east. The two species are sympatric along the Mediterranean-desert transition zone. Flight period: February–April. Flower records: Brassicaceae: Erucaria microcarpa. Additionally, undetermined A. anathema / A. longistilus females were collected from Brassicaceae: Erucaria rostrata, Rapistrum rugosum, Sinapis arvensis, and Plantaginaceae: Plantago lagopus. Holotype: ISRAEL: Horbat Kefar Lakhish, 31.575°N 34.8532°E, 5.iii.2021, G. Pisanty, sweeping, ♂ (SMNHTAU:358873). Paratypes: ISRAEL: Adulam-France Park [Ya’ar Adulam], 2013, Y. Berner (1♀); Beit Guvrin [Bet Guvrin], 28.iii.2010, G. Pisanty, pan trap (1♀); Britannia Park [Park Britanya], 11.ii.2011, T. Koznichki, pan trap (1♀); Dvir [Devira], 12.iv.2009, L. Friedman (1♂) (A. israelica paratype label); Horbat Kefar Lakhish, 31.575°N 34.853°E, 5.iii.2021, G. Pisanty, pan traps (2♂); 15.iii.2021, G. Pisanty, pan traps (2♂); 31.575°N 34.8532°E, 5.iii.2021, G. Pisanty, sweeping (2♂); Horbat Sheqofa, 31.5775°N 34.871°E, 15.iii.2021, G. Pisanty, pan traps (4♂); Lakhish, 22.ii.2012, T. Shapira, pan trap (1♂) (A. israelica paratype label); 21.iii.2013, T. Shapira, pan trap (1♂); 3 km NE, 31.575°N 34.870°E, 4.iii.2016, G. Pisanty (1♂) (A. israelica paratype label); 31.578°N 34.870°E, 19.ii.2016, G. Pisanty (2♂) (A. israelica paratype labels); 26.ii.2016, G. Pisanty (1♀, 1♂) (A. israelica paratype label); Nabi Hazuri, 33.252°N 35.727°E, 27.iv.2020, G. Pisanty (1♀); Nahal Maresha, 220 m, 31.577°N 34.858°E, 15.iii.2021, G. Pisanty, sweeping (1♂); Sasa, 3.iv.2016, O. Winberger (1♀); WEST BANK: Elon More, ‘ En Kefir, 530 m, 17.iii.2015, L. Friedman (1♀); Nofei Prat [NofePerat, Kefar Adummim], north-facing slope of Nahal Perat, 27.ii.2007, L. Friedman (1♂); Wadi Qelt [Nahal Perat], 31.83°N 35.34°E, 14.iii.2015, G. Pisanty (1♀); Za’atara, 6.iii.2015, T. Jumah, on Erucaria microcarpa (1♀) (ES, OLML, RMNH, SMNHTAU, TJW). Etymology. anathema = Greek for “something strongly disliked” in reference to the identification challenges posed by this species. The species epithet is a noun in apposition. Other material examined (undetermined A. anathema / A. longistilus females): ISRAEL: Adulam-France Park [Ya’ar Adullam], 20.iv.2011, T. Koznichki, pan traps (3♀); Arad, 7.ii.1987, E. Shney-Dor (1♀); Beersheba [Negev, Beer Sheva], 30–31.iii.1961 (3♀); Beit Guvrin [Bet Guvrin], 28.iii.2010, G. Pisanty, pan traps (14♀); Beit Nir [Bet Nir], 28.iii.2010, G. Pisanty, pan traps (8♀ + 1♀ stylopised); Bor Mashash, 25.iii.1987, A. Shlagman (1♀ stylopised); Brittania Park [Park Britannia], 24.iv.2011, T. Koznichki, pan traps (5♀); 26.iii.2015, T. Chaprazaro (1♀); 17.iv.2016. T. Chaprazaro (1♀); [Park Britanya], 7.iv.2010, T. Koznichki, pan trap (1♀); 11.ii.2011, T. Koznichki, pan trap (1♀); Degania Alef [Deganya A], 25.iii.1942, Y. Palmoni (1♀); Dimona, 28.iii.1978, D. Furth (1♀); Dvir [Devira], 12.iv.2009, L. Friedman (3♀); Ein Hajla, Rt. 90, 31°49’N 35°30’E, 16.iii.2004, L. Friedman (1♀); Gal’on, 4.iv.2018, T. Roth (1♀); 2 km NW, 31.649°N 34.837°E, 2.iv.2015, G. Pisanty, pan trap (1♀); Ha- Makhtesh HaGadol [Negev, 5 km SE Yeroham, Hamakhtesh Hagadol], 21.iii.1990, R. Leys (1♀); Har Horesha, Rt. 171, 930 m, 2.iv.2014, L. Friedman (9♀); Holot Mash’abbim Nature Reserve [Holot Mash’abbim],], 30.999°N 34.757°E, 10.iii.2017, G. Pisanty (1♀); 30.999°N 34.7575°E, 13.ii.2002, L. Friedman (1♀); 30.999°N 34.7578°E, 13.ii.2002, G. Pisanty, sweeping (1♀); 18.ii.2002, G. Pisanty, pan traps (2♀); Horbat Kefar Lakhish, 31.575°N 34.853°E, 5.iii.2021, G. Pisanty, pan traps (2♀); 15.iii.2021, G. Pisanty, pan traps (5♀); 31.575°N 34.8532°E, 5.iii.2021, G. Pisanty, sweeping (4♀); Horbat Sheqofa, 31.5775°N 34.871°E, 15.iii.2021, G. Pisanty, pan traps (13♀); Kedma [Qedma], 5.iii.2009, G. Pisanty (2♀); Kfar Giladi [Kefar Giladi S], 12.iv.1997, R. Kasher (1♀); 1.5 km N of Kfar Shamai [Kefar Shammay], 650 m, 13.iv.1988, C. O’Toole (1♀); Kfar Shmuel [Kefar Shemuel], 15.ii.1968 (2♀); 25.ii.1968, S. Bleszynski (1♂); 20.iii.1968, S. Bleszynski (1♀); 23.iii.1968, S. Bleszynski (2♀); Kiryat Gat – Beit Kama [Qiryat Gat – Bet Qama], ca. i.2011, I. Van Rijn (5♀); Lakhish, 22.ii.2012, T. Shapira, pan trap (1♀); 23.ii.2012, T. Shapira, pan trap (1♀ stylopised); 21.iii.2012, T. Shapira, pan traps (3♀); 4.ii.2013, T. Shapira, pan traps (1♀); 18.ii.2013, T. Shapira, pan traps (1♀); 6.iii.2013, T. Shapira, pan traps (2♀); 7.iii.2013, T. Shapira, pan traps (1♀); 10.iii.2013, T. Shapira, pan traps (1♀); 14.iii.2013, T. Shapira, pan traps (1♀); 18.iii.2013, T. Shapira, pan traps (1♀); 19.iii.2013, T. Shapira, pan traps (6♀); 20.iii.2013, T. Shapira, pan traps (2♀ + 1♀ stylopised); 13.iv.2013, T. Shapira, pan traps (2♀); 3 km NE, 31.575°N 34.870°E, 4.iii.2016, G. Pisanty (1♀); 11.iii.2016, G. Pisanty, partly from pan traps (4♀); 31.578°N 34.870°E, 26.ii.2016, G. Pisanty (1♀); 19.iii.2016, G. Pisanty, partly from pan traps (2♀); 31.579°N 34.871°E, 4.iii.2016, G. Pisanty, pan trap (1♀) and on Sinapis (1♀); Lehavim, 31.365°N 34.830°E, 28.i.2015, G. Pisanty, partly from pan traps (14♀); 31.370°N 34.8257°E, 7.iii.2015, G. Pisanty, pan traps (6♀ + 3♀ stylopised); Ma’agar Yeroham, 30°59’N 34°55’E, 5.iv.2007, S. Chaviv & N. Greenman (1♀); Mitzpe Ramon [Mizpe Ramon], 30 km SW Har Ramon, 10.iv.1990, K. Warncke (1♀) (A. avedata paratype label); Nahal Dishon, 1.iv.1991, R. Kasher (1♀); Nahal Gerar, 31.3998°N 34.470°E, 21.i.2015, G. Pisanty, pan trap (1♀); Nahal Maresha, 220 m, 31.577°N 34.858°E, 15.iii.2021, G. Pisanty, pan traps (2♀) and sweeping (2♀); Nahal Me’arot, 8.iv.1988, I. Yarom (1♀); Nahal Revivim [N. Rvivim], 4.iv.1988, Y. Zvik (1♀); Nahal Tahmas, 16.iii.1999, L. Friedman (1♀); Nahal Yavne’el spill, 17.iii.1942, Y. Palmoni (1♀); Nahal Ye’elim, 6.iv.1988, F. Kaplan (1♀) & I. Yarom (1♀); Nahal Ye’elim, Rt. 31, 20.iv.2015, L. Friedman (2♀); Nahshon, 25.ii.2009, G. Pisanty (1♀); Northern Negev, 27.iii.2015, G. Pisanty (2♀); Pura Nature Reserve, 31.496°N 34.778°E, 27.iii.2015, G. Pisanty (1♀); 200 m, 31°29.7’N 34°46.8’E, 18.iii.2010, A. Freidberg (1♀); Retamim, 273 m, 31°03’N 34°41.5’E, 3.iv.2009, A. Freidberg (1♀); Revivim, 12.iii.1974, D. Furth (1♀); Sasa, 3.iv.2016, O. Winberger (2♀); Sde Boker [Sde Boqer], 28.iii.1978, D. Furth (2♀); 3 km N [Sede-Boqer], 19.ii.1995, R. Kasher (1♀); 8.iii.1995, R. Kasher (1♀); Shivta, 17.iii.1977, A. Freidberg (3♀ + 1♀ stylopised, 1♂); Shivta Junction, 30.941°N 34.597°E, 16.iii.2020, G. Pisanty, pan traps (2♀); [Holot Shunera], 30.941°N 34.597°E, 17.iii.2017, G. Pisanty (5♀ + 1♀ stylopised); Tel Yeroham [Tel-Jerucham], 25.iii.1959, J. Kugler, on Erucaria microcarpa (2♀); Tell es-Safi [Tel Zafit], 7.iii.2018, T. Roth, on Plantago lagopus (1♀); 31.iii.2018, T. Roth, partly on Rapistrum rugosum (3♀); Yeruham [Kfar-Jerucham], 24.iii.1959, I. Kugler (1♀ stylopised); [Yeroham], 2 km E, 21.iii.1990, R. Leys (1♀); JORDAN: Al-Maghtas, 10.iv.1943, H. BytinskiSalz (1♀); Dana, 3.v.2012, M. Kafka (630♀, 66♂); Kerak env. [Al Karak env.], 6.iv.2013, M. Snižek (2♀); 15 km W Madaba, 760 m, 27.iv.2006, K. Deneš (1♀); SYRIA: 30 km W Palmyra, 580 m, 23.iv.1992, K. Warncke (2♀); 110 km E of Palmyra, 350 m, 21–22.iv.1992, K. Warncke (5♀); WEST BANK: Almog, 10 km S Jericho, – 350 m, 3.ii.1990, R. Kasher, on Erucaria rostrata (1♀); Elon More, ‘En Kefir, 530 m, 17.iii.2015, L. Friedman (1♀); Herodium [Herodyon], 31°40’N 35°14’E, 31.iii.2009, M. Guershon (1♀); Ma’on, 0–1 km S, 750–800 m, 14.iv.2015, L. Friedman (2♀); Maskiot [Maskiyyot], Rt. 578, Wadi Halat Mahmud el-‘Ali, – 75 m, 32°19’18’’N 35°29’52’’E, 27.ii.2020, L. Friedman (1♀); Mehola, Rt. 578, – 177 m, 32°21’48’’N 35°30’49’’E, 27.ii.2020, L. Friedman (2♀); Nofei Prat [NofePerat, Kefar Adummim], north-facing slope of Nahal Perat, 27.ii.2007, L. Friedman (4♀); Ubeidiya, 6.iv.2014, I. Arar, on Sinapis arvensis (1♀ + 1♀ stylopised); Za’atara, 14.iv.2014, I. Arar, on Erucaria rostrata (1♀) (CNC, OLML, RMNH, SMNHTAU, TJW).
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- 2022
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18. Andrena (Aciandrena) longistilus Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
- Author
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy ,Andrena longistilus - Abstract
Andrena (Aciandrena) longistilus Pisanty & Wood sp. nov. (Figs. 18–26) Female (Fig. 18). Body length: 5–5.5 mm. Colour. Head and mesosoma dark brown to black (Fig. 18). Metasoma brown to black. Anterior side of flagellomeres 4–10 orange. Legs brown (Fig. 18). Wings hyaline to slightly infuscate, veins light to dark brown, stigma golden. Tergal marginal zones golden, sometimes reddish basally (Fig. 21). Pubescence. Body hair mostly short and sparse, minutely plumose, white to golden (Fig. 18). Clypeus with sparse, short, thin white to yellowish hair. Paraocular area and scape with moderately dense, short white to yellowish hair (Fig. 19). Facial foveae black in ventral view, white to brownish in dorsal view (Fig. 20). Vertex and genal area with short white to golden hair. Mesonotum, scutellum and metanotum with short whitish to golden hair, sparse on center of mesonotum and anterior half of scutellum, dense and thick (almost scale-like) elsewhere (Fig. 20). Mesepisternum with long white hair. Propodeal corbicula incomplete, dorsoposterior fringe with long white plumose hair, corbicular surface with few long white simple hairs. Leg hair mostly white; scopal hair simple, white; flocculus incomplete, white (Fig. 18). Tergal discs 1–2 hairless, 3–4 with sparse inconspicuous minute white hairs, denser on 4. Tergal marginal zones 2–4 with moderately dense bands of short white hair, interrupted on 2–3, continuous on 4. Prepygidial fimbria white laterally, golden medially; pygidial fimbria golden (Fig. 21). Head (Figs. 19–20). 1.2 times broader than long. Mandible bidentate. Galea shagreened. Labral process triangular to narrowly trapezoidal. Clypeus strongly flattened medially, finely shagreened, occasionally with a smooth apical region up to 1/3 of clypeus height, shallowly and finely punctured, distance between punctures 1–2 puncture diameters, punctures gradually sparser medially, an impunctate midline is not indicated (Fig. 19). Supraclypeal plate finely and shallowly shagreened, not striated. Flagellomere 1 slightly shorter than 2+3. Frons finely and shallowly longitudinally striated. Facial foveae tapering downwards, extending from level of middle–lower end of lateral ocellus to middle of antennal socket, about 0.4 times as broad as antennocular distance (Fig. 19). Distance of fovea from lateral ocellus 1 ocellus diameter. Ocelloccipital distance about 0.5 ocellus diameter. Vertex moderately carinate (Fig. 20). Mesosoma (Fig. 20). Mesonotum and scutellum shiny, weakly but uniformly shagreened, punctation fine, extremely shallow and inconspicuous, distance between punctures 1–3 puncture diameters (Fig. 20). Mesepisternum and propodeum finely reticulate-alveolate. Propodeal triangle delineated by carina, sculpturing much coarser than on flanking areas (Fig. 20). Hind pretarsal claw unidentate. Recurrent vein 1 meets submarginal cell 2 at its proximal 1/3–1/2. Submarginal crossvein 1 meets marginal cell 1–2 vein widths from stigma. Nervulus antefurcal. Metasoma (Fig. 21). Tergal discs impunctate, 1–3 strongly shagreened, 4 more shallowly so. Tergal marginal zones similar, smooth near apex, slightly arched, medially covering 1/3–1/2 of tergum length, 2–4 weakly depressed. Male (Fig. 22). Body length: 4.5 mm. Colour. Similar to female (clypeus and paraocular area dark, one male from Kerak, Jordan with clypeus yellow centrally), generally somewhat darker, flagellum reddish-brown apically, tergal marginal zones more reddish (Fig. 22). Pubescence. Clypeus with short white hairs, dense apicolaterally, moderately dense elsewhere. Paraocular area and scape with moderately dense, medium-lengthed white to yellowish hair (Fig. 23). Vertex with short to medium, white to yellowish hair. Genal area with white to yellowish short hair dorsally, short to medium white hair ventrally. Mesonotum, scutellum and metanotum with moderately dense, medium-lengthed white to brownish hair (Fig. 24). Mesepisternum and propodeum with long white hair. Legs with mostly white hair. Tergal discs with short hair laterally, minute inconspicuous white hair medially. Tergal marginal zones 2–4 with moderately dense bands of white hair, interrupted on 2–3, almost continuous on 4 (Fig. 22). Head (Figs. 23–24). 1.2 times broader than long. Labral process trapezoidal, apex bifurcate. Clypeus strongly flattened medially, weakly shagreened basally, smooth apically, finely punctured, distance between punctures 1–3 puncture diameters, punctation sparser apically, without impunctate midline (Fig. 23). Supraclypeal plate finely and shallowly shagreened, not striated. Flagellomere 1 about as long as 4, 2 slightly shorter than 3. Frons finely and shallowly longitudinally striated (Fig. 23). Ocelloccipital distance 0.7 ocellus diameter. Vertex carinate (Fig. 24). Mesosoma (Fig. 24). Similar to female, but hind leg pretarsal claw bidentate. Metasoma. Similar to female. Genitalia and hidden sterna (Figs. 25–26). Dorsal lobe of gonoxocite not developed. Gonostyli very elongate, almost straight, spatulate, gradually broadening apically. Penis valves narrow, tapering apically (Fig. 25). Sternum 8 simple, columnar, apical process slightly and gradually broadened (Fig. 26). Diagnosis. For the female of A. longistilus, see corresponding section in A. anathema sp. nov. The males of A. longistilus are easily identified by their elongate gonostyli (Fig. 25), which are unique among Aciandrena species. Distribution: Semi-arid to arid habitats in central and southern Israel, Jordan, Syria and the West Bank. Seems to exhibit a vicariance pattern with A. anathema sp. nov., with A. anathema mostly occupying more mesic habitats in north and central Israel. The two species are sympatric along the Mediterranean-desert transition zone. Flight period: January–May. Flower records: Undetermined A. anathema / A. longistilus females were collected from Brassicaceae: Erucaria microcarpa, Erucaria rostrata, Rapistrum rugosum, Sinapis arvensis, and Plantaginaceae: Plantago lagopus. Holotype: ISRAEL: Shivta Junction, 30.941ºN 34.597ºE, 17.iii.2017, G. Pisanty, pan trap, ♂ (SMNHTAU:269112). Paratypes: ISRAEL: Arad, 570 m, 31°15.346’N 35°11.958’E, 7.iii.2010, A. Freidberg (1♂); Avdat [Avedat], 16.iii.1988, A. Freidberg (1♂) & A. Shlagman (2♂); 10.iv.1990, K. Warncke (1♂) (A. avedata paratype label); Bor Hemet, 19.iv.2001, L. Friedman (1♂); Borot Loz, 930 m, 23.iii.2020, L. Friedman (1♀); Ein Yahav [‘En Yahav], 8.iii.2009, A. Gotlieb (1♀); Har Horesha, Rt. 171, 930 m, 2.iv.2014, L. Friedman (1♀); Holot Mash’abbim Nature Reserve [Holot Mash’abbim], 30.999°N 34.7575°E, 13.ii.2022, L. Friedman (2♂); 30.999°N 34.7578°E, 18.ii.2022, G. Pisanty, pan trap (1♂); 31.000°N 34.756°E, 16.iii.2020, G. Pisanty, pan traps (1♂); Kiryat Gat – Beit Kama [Qiryat Gat – Bet Qama], ca. i.2011, I. Van Rijn (2♂); Lakhish, 4.ii.2013, T. Shapira, pan trap (1♂); [Lachish], 9.iii.2020, K. Levy, pan trap (1♂); Lehavim, 31.365°N 34.830°E, 28.i.2015, G. Pisanty, partly from pan traps (1♀, 23♂); 31.370°N 34.8257°E, 7.iii.2015, G. Pisanty, pan traps (1♂); Nahal Zin, 15.iv.2007, I. Lalzar (1♀); Retamim, 273 m, 31°03’N 34°41.5’E, 3.iv.2009, A. Freidberg (2♂); Sa’ad, 31.468°N 34.5287°E, 21.i.2015, G. Pisanty, pan traps (2♂); Sde Boker [Sde Boqer], 28.iii.1978, D. Furth (1♂); 3 km N [Sede-Boqer], 19.ii.1995, R. Kasher (3♂); Shivta, 17.iii.1977, A. Freidberg (1♂); Shivta Junction [Holot Shunera], 30.941°N 34.597°E, 10.iii.2017, G. Pisanty (2♂); 17.iii.2017, G. Pisanty (5♂); JORDAN: Dana, 3.v.2012, M. Kafka (3♂); Kerak, 1000 m, 27.ii.1986, K.M. Guichard (1♂); Kerak env. [Al Karak env.], 6.iv.2013, M. Snižek (3♂); SYRIA: 110 km E of Palmyra, 350 m, 21–22.iv.1992, K. Warncke (3♂); WEST BANK: Kfar Adumim [NahalPerat, north-facing slope, Kefar Adummim], 27.ii.2007, A. Freidberg (2♂); [NofePerat, Kefar Adummim, north-facing slope of Nahal Perat], 27.ii.2007, L. Friedman (1♂) (ES, NHMUK, OLML, RMNH, SMNHTAU, TJW, ZSMC). Etymology. longistilus = Latin for “long stick”, referring to the notable length of the gonostyli in the male genital capsule. The species epithet is a noun in apposition. Other material examined (undetermined A. anathema / A. longistilus females): see corresponding section in A. anathema sp. nov. Remarks. This taxon was recognised as new by Klaus Warncke under the name A. avedata, though he died in 1993 before he could publish a description of this species (see Pisanty et al. 2016). Andrena avedata is therefore a nomen nudum, and we have chosen a clearly different name to avoid confusion.
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- 2022
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19. Andrena (Avandrena) euphorbiae Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
- Author
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Insecta ,Andrena euphorbiae ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Avandrena) euphorbiae Pisanty sp. nov. (Figs. 50–57) Female (Fig. 50). Body length: 7–7.5 mm. Colour. Body and legs dark brown to black (Fig. 50). Anterior side of flagellomeres 3–10 orange. Apical tarsomeres orange. Wings hyaline, veins brown, stigma tan medially. Tergal marginal zones yellowish-brown (Fig. 53). Pubescence. Supraclypeal area, vertex, basal half of clypeus, lower half of frons, and area around antennal sockets with mixed whitish and dark, medium to long plumose hairs; apical half of clypeus with long, brown simple hairs (Fig. 51). Facial foveae brownish. Genal area with medium-lengthed whitish to golden hairs. Mesonotum, scutellum and metanotum with medium-lengthed, whitish to golden plumose hairs (Fig. 52). Mesepisternum with long plumose hairs, mostly dark on dorsal 1/3, whitish to golden on ventral 2/3. Propodeal corbicula incomplete, dorsoposterior fringe with long, white to golden plumose hairs, corbicular surface with few simple bright hairs. Leg hair mostly short, white to brown, fore femur with some black hair near apex (Fig. 50). Flocculus complete. Tibial scopal hairs simple, whitish (Fig. 50). Tergal discs with sparse, weakly plumose whitish hairs, short to long on tergum 1, short on terga 2–4. Tergal marginal zones 2–4 with distinct bands of white hair extending onto following disc, interrupted on tergum 2, almost complete on 3, complete on 4. Terminal fringe brownish (Fig. 53). Head (Figs. 51–52). 1.3 times broader than long. Labral process triangular, apex pointed. Clypeus medially flattened, very shiny, basal half superficially shagreened, apical half more or less smooth, punctation weak, of moderate size, distance between punctures 1.5 puncture diameters, with medioapical impunctate area (Fig. 51). Flagellomere 1 as long as 2+3 or slightly shorter, 2 about as long as 3. Frons longitudinally striated. Facial foveae short, broad and shallow, drop-shaped, extending from level of lower end of lateral ocellus to upper half of antennal socket, 0.7 times as broad as antennocular distance (Figs. 51–52). Distance of fovea from lateral ocellus about 1.5 ocellus diameters. Ocelloccipital distance 1.5 ocellus diameters. Vertex moderately carinate (Fig. 52). Mesosoma (Fig. 52). Dorsolateral angle of pronotum not elevated, pronotum not carinate. Mesonotum weakly shiny, strongly and completely shagreened, impunctate except for a few shallow oblique punctures medially (Fig. 52). Scutellum similar, more strongly shiny. Mesepisternum and posterolateral part of propodeum finely alveolate. Propodeal corbicula finely reticulate. Propodeal triangle narrow, radially rugose on basal 1/4–1/2, very finely alveolate apically. Inner side of hind femur rounded, not carinate, without spines. Inner hind tibial spur more less straight and of uniform width. Hind leg pretarsal claw with distinct inner tooth. Nervulus antefurcal. Recurrent vein 1 meets submarginal cell 2 at its middle or distal to it. Metasoma (Fig. 53). Basal half of tergal disc 1 smooth; apical half and tergal discs 2–4 shiny, superficially shagreened, sparsely, inconspicuously and very finely punctured, distance between punctures 2–3 puncture diameters. Tergal marginal zones similarly superficially shagreened and shiny, slightly depressed, hardly discernible from discs. Pygidial plate not elevated medially. Male (Fig. 54). Body length: 6.5–7 mm. Colour. Head and mesosoma dark brown to black (Fig. 54). Clypeus and paraocular areas dark (Fig. 55). Anterior side of flagellomeres 2–11 light brown (Figs. 54–55). Legs and metasoma brown to black. Wings hyaline, veins brown, stigma tan medially (Fig. 54). Pubescence. Face covered with long hairs up to antennal sockets, dark on paraocular areas and lateral parts of clypeus, whitish on centre of clypeus, black and white around antennal sockets (Fig. 55). Vertex with whitish hairs (Fig. 54). Genal area with dark hairs anteriodorsally, whitish hairs elsewhere. Mesosoma with medium to long, whitish plumose hairs. Leg hair mostly white to brown, fore femur with some dark hair near apex. Tergal discs with sparse whitish hairs, short to medium on terga 1–2, short on terga 3–5. Tergal marginal zones 2–4 with distinct bands of white hair extending onto following disc, interrupted on terga 2–3, complete on 4 (Fig. 54). Tergal marginal zones 5–6 with sparse, long whitish hairs. Head (Figs. 55–56). 1.3 times broader than long. Labral process weakly trapezoidal, apical margin distinctly emarginate. Clypeus weakly convex, shagreened basally and shiny apically, densely and shallowly punctured, distance between punctures 0.5–1 puncture diameters, without impunctate midline (Fig. 55). Flagellomere 1 slightly shorter than 2, 2 slightly shorter than 3. Frons longitudinally striated. Ocelloccipital distance about 1.5 ocellus diameters. Vertex distinctly carinate (Fig. 56). Posterior margin of genal area not carinate. Mesosoma (Fig. 56). Similar to female. Metasoma. Similar to female. Genitalia and hidden sterna (Fig. 57). Dorsal gonocoxite lobes developed, narrow, rounded apically. Gonostylus elongate, gradually broadening apically, blade flattened, rounded apically. Penis valves long and narrow, of uniform width (Fig. 57). Sternum 8 columnar, apical process broadened. Diagnosis. Andrena euphorbiae belongs to a group of Avandrena lacking female femoral spines, whose phylogenetic placement is uncertain (Pisanty et al. 2022). This group includes also A. canohirta (Friese), A. caudata Warncke, A. melacana Warncke and A. ochropa Warncke (Warncke 1980). The female of A. euphorbiae is distinguished from these species by the triangular labral process (indented rectangular in all four species), normal clypeus edge (anteriorly curved in A. melacana), non-carinate pronotum (weakly carinate in A. canohirta and A. melacana, strongly so in A. ochropa), shagreened mesonotum and scutellum (partly to fully smooth in A. canohirta, A. caudata and A. melacana), simple-haired scopa (plumose in A. caudata), and shagreened terga (smooth in A. canohirta). The male of A. euphorbiae is easily distinguished from all other Avandrena by its simple, unmodified genital capsule, with narrow penis valves (Fig. 57). Distribution: North and central Israel. Flight period: February–April. Flower records: Euphorbiaceae: Euphorbia hierosolymitana. Pollen preferences: Four analysed loads from Ramat HaNadiv and Matlul Avinadav contained pure Euphorbia pollen, confirming the field observations. One analysed load from Ramat Hadassa visually contained much larger grains, but these also belonged to Euphorbia, though clearly of a different species. Andrena euphorbiae would therefore seem to be a specialist of Euphorbia, the first bee species to our knowledge to be documented as such. Holotype: ISRAEL: Mevo Hama Forest, 32.709ºN 35.6495ºE, 1.iii.2022, G. Pisanty, on Euphorbia hierosolymitana, ♀ (SMNHTAU:385097) Paratypes: ISRAEL: Bethlehem of Galilee [Bet Lehem haGelilit], 10.iii.1997, L. Friedman (1♀); Karei Deshe [Kare Deshe], 19.iii.2012, T. Shapira, pan trap (1♂); Malkia [Malkiyya], 10.iv.2014, O. Winberger (2♀); 13.iv.2014, O. Winberger (1♀); Matlul Avinadav, 32.46ºN 35.435ºE, 19.ii.2019, G. Pisanty, on Euphorbia hierosolymitana (1♀); Ramat Hadassa, 3.iv.1963 (1♀); Ramat HaNadiv, 22.iii.2012, T. Shapira (1♀); 32.551ºN 34.945ºE, 15.ii.2021, G. Pisanty, on Euphorbia hierosolymitana (7♀, 1♂) (OLML, RMNH, SMNHTAU, TJW). Etymology. From Euphorbia, in reference to the species’ host plant. The species epithet is an adjective., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 28-29, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Pisanty, G., Richter, R., Martin, T., Dettman, J. & Cardinal, S. (2022) Molecular phylogeny, historical biogeography and revised classifcation of andrenine bees (Hymenoptera: Andrenidae). Molecular Phylogenetics and Evolution, 170, 107151.","Warncke, K. (1980) Zur Verbreitung der Bienengattung Andrena F. in Tunesien (Hymenoptera, Apidae). Mitteilungen der Munchner Entomologischen Gesellschaft, 70, 65 - 87."]}
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20. Andrena (Pallandrena) christineae Dubitzky 2006
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena christineae ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Pallandrena) christineae Dubitzky, 2006 Distribution: Israel (first record), Iran, Lebanon, Turkey. Likely present also in Syria. Flight period: April–June (Dubitzky 2006; Wood et al. 2020a). Flower records: Geraniaceae: Geranium libanoticum (Wood et al. 2020a). Material examined: ISRAEL: Mount Hermon, 2000 m, 28.v.1985, J. Kugler (1♀); TURKEY: 10 km N Tutak, Ağrı, 1500 m, K. Warncke, 7.vi.1981 (1♀) (OLML, SMNHTAU)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 61, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Dubitzky, A. (2006) New palearctic species of the bee genus Andrena (Insecta: Hymenoptera: Andrenidae). Zootaxa, 1284, 1 - 27.","Wood, T. J., Boustani, M. & Rasmont, P. (2020 a) A revision of the Andrena (Hymenoptera: Andrenidae) of Lebanon with the description of six new species. Annales de la Societe Entomologique de France, 56, 279 - 312. https: // doi. org / 10.1080 / 00379271.2020.1794960"]}
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21. Andrena (Chlorandrena) humilis Imhoff 1832
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Andrena humilis ,Hymenoptera ,Taxonomy - Abstract
Andrena (Chlorandrena) humilis Imhoff, 1832 Distribution: Europe, north-western Africa, Turkey, Lebanon, and eastwards into Russia and the Caucasus (Gusenleitner & Schwarz 2002; Hazir et al. 2014; Wood et al. 2020a). Remarks. The presence of this species in Israel is mentioned as questionable by Warncke, based on a single female collected by Schmiedeknecht, apparently in Jerusalem (Warncke 1969). We have not seen any verified records of A. humilis south of Lebanon, and the specimen mentioned by Warncke may belong to A. tadauchii, which he regarded as a subspecies of A. humilis (A. h. prunella Warncke, 1975 nec Warncke, 1974, see above)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 101, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Imhoff, L. (1832) Entomologica. Isis, Oken, Jena, 1832, 1198 - 1208.","Gusenleitner, F. & Schwarz, M. (2002) Weltweite Checkliste der Bienengattung Andrena mit Bemerkungen und Erganzungen zu palaarktischen Arten (Hymenoptera, Apidae, Andreninae, Andrena). Entomofauna, Supplement 10, 1 - 1280.","Hazir, C., Keskin, N. & Scheuchl, E. (2014) Faunistic, geographical and biological contributions to the bee genus Andrena (Hymenoptera, Andrenidae, Andreninae) from Turkey. Journal of Hymenoptera Research, 38, 59 - 133. https: // doi. org / 10.3897 / jhr. 38.7288","Wood, T. J., Boustani, M. & Rasmont, P. (2020 a) A revision of the Andrena (Hymenoptera: Andrenidae) of Lebanon with the description of six new species. Annales de la Societe Entomologique de France, 56, 279 - 312. https: // doi. org / 10.1080 / 00379271.2020.1794960","Warncke, K. (1969) A contribution to the knowledge of the genus Andrena (Apoidea) in Israel. Israel Journal of Entomology, 4, 377 - 408.","Warncke, K. (1975) Die Sandbienen der Turkei (Hymenoptera, Apoidea, Andrena), Teil B. Beschreibungen der neuen Andrena - Arten bzw. Unterarten. Mitteilungen der Munchner Entomologischen Gesellschaft, 65, 29 - 102."]}
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22. Andrena (Euandrena) igraeca Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena igraeca ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Euandrena) igraeca Pisanty & Wood sp. nov. (Figs. 86–95) Female (Fig. 89). Body length: 8–8.5 mm. Colour. Head and ventrolateral part of mesosoma black (Figs. 86, 89). Anterior side of flagellum brown to black (Fig. 86). Mesonotum, scutellum and metanotum dark with bluish metallic luster (Fig. 87). Legs and metasoma brown to black (Fig. 89). Wings hyaline, veins and stigma brown. Tergal marginal zones yellowish (Fig. 88). Pubescence. Clypeus and area around antennal sockets with medium-lengthed golden hair (Fig. 86). Outer half of paraocular area with short to medium black hair. Scape with short black hairs. Frons with short to long black hairs. Facial foveae brown (Fig. 87). Vertex with long, erect golden and black hairs. Genal area with short black hair anteriodorsally, short to medium golden hair posteroventrally. All parts of mesosoma covered with medium to long, erect golden hair (Figs. 87, 89). Propodeal corbicula incomplete, posterodorsal fringe with dense, long golden hairs, corbicular surface with long sparsely plumose golden hairs. Leg hair golden to brown (Fig. 89). Flocculus incomplete, yellowish. Femoral and tibial scopal hairs sparsely plumose, golden (Fig. 89). Tergal discs with sparse short to medium golden hair, longer on lateral parts of terga 1–2. Tergal marginal zones 1–4 with strong continuous bands of dense, medium-lengthed yellowish-golden hair, arising from base of marginal zone and extending onto base of following disc, longer on tergum 1. Terminal fringe brown (Fig. 88). Head (Figs. 86–87). 1.2 times broader than long. Mandible bidentate. Galea shagreened. Labral process broad, trapezoidal, basal half transversely striated, apical half smooth, apical margin weakly concave. Clypeus moderately convex, shagreened basally, gradually smooth apically, distinctly punctured, distance between punctures 1 puncture diameters, without impunctate midline, apical margin mostly impunctate (Fig. 86). Lower part of paraocular area finely shagreened, finely punctured. Flagellomere 1 longer than 2+3, 2 as long as 3. Frons longitudinally striated. Facial foveae short, extending from level of lower end of lateral ocellus to lower end of antennal socket, 0.4 times as broad as antennocular distance (Figs. 86–87). Distance of fovea from lateral ocellus about 1.1 ocellus diameters. Ocelloccipital distance about 1 ocellus diameter. Vertex moderately carinate (Fig. 87). Mesosoma (Fig. 87). Dorsolateral angle of pronotum not elevated, pronotum not carinate. Mesonotum and scutellum shiny but strongly, uniformly and finely shagreened, punctation dense and coarse, extremely superficial and often almost indistinguishable from shagreenation, distance between punctures 0.5–1 puncture diameters (Fig. 87). Mesepisternum and posterolateral part of propodeum finely alveolate-reticulate, densely, shallowly and obliquely punctured, punctures merging into reticulation. Propodeal corbicula finely reticulate, sparsely and coarsely, obliquely punctured. Propodeal triangle T-shaped, very finely alveolate, basal margin radially rugose (Fig. 87). Hind leg pretarsal claw bidentate. Nervulus more or less interstitial. Metasoma (Fig. 88). Tergal discs shiny, weakly to moderately shagreened, very finely punctured, distance between punctures about 2 puncture diameters, apical half of disc 1 often with crater-like punctures. Tergal marginal zones shagreened, apical margin smooth. Pygidial plate without elevated medial area. Male (Fig. 90). Body length: 6.5 mm. Colour. Head and mesosoma black, non-metallic (Figs. 90–92). Anterior side of flagellomeres 2–11 dark brown (Figs. 90–91). Legs and metasoma dark brown to black (Figs. 90, 93). Wings hyaline, veins and stigma dark brown (Fig. 90). Tergal marginal zones reddish-yellowish (Fig. 93). Pubescence. Clypeal hair long, two-coloured, varying among specimens from mostly black with an apical fringe of golden hairs, to mostly golden with small lateral patches of black hair (Figs. 90–91). Paraocular area with long black hair. Area around antennal sockets with medium to long golden hair. Scape with medium-lengthed golden and black hairs. Frons with medium to long black hairs. Vertex with long, erect golden hairs. Genal area with medium-lengthed black hair anteriodorsally, medium to long golden hair posteroventrally. All parts of mesosoma covered with medium to long, erect golden hair (Figs. 90, 92). Leg hair mostly golden, sometimes with few black hairs on femora and tibiae (Fig. 90). Tergal discs with sparse white to golden hair, short centrally, long on lateral parts of disc 1, gradually shorter on lateral parts of following terga. Tergal marginal zones 1–5 with strong continuous bands of dense, medium-lengthed white to golden hair, arising from base of marginal zone and extending onto base of following disc, longer on tergum 1. Terminal fringe light brown (Fig. 93). Head (Figs. 91–92). Clypeus not protuberant, often centrally flattened, basal half shagreened, apical half shagreened to smooth, punctation dense, distance between punctures 0.5–1 puncture diameters, without impunctate midline. Flagellomere 1 longer than 3, 2 shorter than 3. Rest of head as in female. Mesosoma (Fig. 92). Similar to female, but mesonotum and scutellum mat, punctation sparser, distance between punctures 1–2 puncture diameters (Fig. 92). Metasoma (Fig. 93). Similar to female. Genitalia and hidden sterna (Figs. 94–95). Dorsal lobes of gonocoxite distinct, broad and rounded. Gonostyli narrow basally, blade flattened and broadened, inner margin convex, outer margin concave, apex pointed. Basal half of penis valves of moderate, uniform width, with a narrow, arched flanking lamella; apical half tapering (Fig. 94). Sternum 8 Y-shaped, with a columnar stem and a distinctly bilobed apical process (Fig. 95). Diagnosis. Andrena igraeca is closely related to A. rufula Schmiedeknecht. The female is distinguished from most Euandrena by the strongly shagreened and mat, imperceptibly punctured, metallic-hued mesonotum (Fig. 87). It differs from A. rufula in the smaller body size, stronger metallic hue of the mesonotum, and presence of distinct yellowish tergal apical hair bands (tergal discs and marginal zones in A. rufula more or less uniformly covered in orange-brown hair, not forming distinct apical hair bands). The male of A. igraeca is easily distinguished from all other Euandrena by the unique genital capsule and sternum 8 (Figs. 94–95). It differs from A. rufula in the smaller body size, distinct dorsal gonocoxite lobe (weakly produced and truncate in A. rufula), broader penis valves, and strongly bifurcate, Y-shaped sternum 8 (normally built in A. rufula, with an apical notch). Andrena scrophulariae Wood also possesses a Y-shaped sternum 8, but it has a much broader gonostylus blade (Fig. 100), and a longer, very smooth clypeus (Fig. 96). Distribution: North and central Israel, Lebanon, Syria. Likely present also in Hatay province, Turkey. Flight period: February–April. Flower records: Brassicaceae: Sinapis alba; Lamiaceae: Salvia rosmarinus; Plantaginaceae: Veronica syriaca; Rosaceae: Prunus dulcis. Holotype: ISRAEL: Horbat Kefar Lakhish, 31.575°N 34.853°E, 5.iii.2021, G. Pisanty, pan trap, ♂ (SMNHTAU:358922). Paratypes: ISRAEL: Bet Me’ir, 18 km W [E] Jerusalem, 4.iii.1990, T. Boker, on Sinapis alba (1♀); Har Avital, Golan Heights, 15.iii.1995, R. Kasher (1♀, 7♂); Horbat Kefar Lakhish, 31.575°N 34.853°E, 5.iii.2021, G. Pisanty, pan trap (1♀, 3♂); 15.iii.2021, G. Pisanty, pan trap (3♀, 7♂); Jerusalem, 18.iii.1991, R. Kasher, on Salvia rosmarinus (1♀); 24.ii.2014, A. Gotlieb (3♂); 700 m, 5.iii.1975, K.M. Guichard (1♀); Kfar Menahem [Kefar Menahem], 1.iii.2008, G. Pisanty (1♀); Kokhav Ya’ir, Ya’ar Sappir, 32°13.9’N 34°59.5’E, 160 m, 16.ii.2010, L. Friedman (1♀); Montfort, 17.iii.1983, F. Kaplan (1♀); [Montfort, Nahal Keziv], 28.ii.2018, G. Pisanty (1♂); Mount Carmel, 4.iii.1975, F. Kaplan (1♀); Mount Carmel, Hay-Bar, 1 km S University, 25.iii.1990, R. Kasher (1♀); Mount Hermon [Har Hermon], 1610 m, 33.300°N 35.767°E, 7.iv.2021, G. Pisanty, pan trap (2♂); 1642 m, 33.2996°N 35.7677°E, 16.iv.2022, G. Pisanty, pan traps (1♀, 5♂); [Hermon], 1641 m, 33.2993°N 35.7670°E, 16.iv.2022, G. Pisanty, on Prunus dulcis (1♀); Mount Hermon Nature Reserve, 21.iv.2012, G. Pisanty (1♂); Mount Meron [Har Meron], 33.000°N 35.3927°E, 4.iv.2017, G. Pisanty, pan trap (2♀); 1000 m, 1.iv.2012, L. Friedman (1♀); Nahal Kziv [Nahal Keziv], 33°02.7’N 35°13.6’E, 5.iii.2008, A. Freidberg (1♂); Odem Forest Nature Reserve [Ya’ar Odem N.R.], 1.iii.2018, G. Pisanty (4♂); [Ya’ar Odem NR], 33.186°N 35.7356°E, 27.ii.2020, G. Pisanty, pan trap (1♂); LEBANON: Horch Ehden, Nabeh Jouit, 1336 m, 24.iv.2019, M. Boustani, on Veronica syriaca (1♀); SYRIA: Kesab [Kassab] env., 28.iii.1994, J. & S. Becvar (1♀) (NHMUK, OLML, RMNH, SMNHTAU, TJW). Etymology. i graeca is the Latin name for the Roman letter Υ, in reference to the ‘Y’ shaped sternum 8 of the male. The species epithet is a noun in apposition.
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23. Andrena (incertae sedis) asluji Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (incertae sedis) asluji Pisanty sp. nov. (Figs. 195–203) Female (Fig. 198). Body length: 6.5–7 mm. Colour. Clypeus, supraclypeal area and lower half of paraocular area black. Frons and upper half of paraocular area dark with bluish-bronze metallic luster (Fig. 195). Anterior side of flagellomeres 4–10 orange (Figs. 195, 198). Genal area black, dorsal part sometimes with metallic luster. Mesosoma black, mesonotum with bronze-bluish metallic luster (Fig. 196). Legs dark brown, apical tarsomeres reddish-brown. Wings hyaline, veins brown, stigma orange to brown peripherally, yellowish-orange medially (Fig. 198). Tergal disc 1 reddish medially and apicolaterally, black basolaterally; 2 reddish with black lateral maculations; 3–5 ranging from fully reddish to mostly black. Tergal marginal zones yellowish (Fig. 197). Pubescence. Clypeus with short, thin white hairs. Paraocular area and area around antennal sockets with thicker, medium white to yellowish hairs (Fig. 195). Facial foveae with dense minute hairs appearing black in ventral view, whitish to golden in dorsal view (Figs. 195–196). Vertex with short to medium, white to golden hairs. Genal area with dense, short to medium white hairs. Mesonotum with short, whitish to golden hairs. Posterolateral margin of scutellum with dense, medium yellowish to golden hairs (Fig. 196). Mesepisternum with long white hairs. Propodeal corbicula incomplete, dorsoposterior fringe with long, white plumose hairs. Corbicular surface with white simple hairs, mostly minute, a few medium-lengthed. Leg hair mostly white to whitish (Fig. 198). Scopal hairs simple, whitish, relatively short and sparse, underlying cuticle clearly visible. Flocculus incomplete, white. Tergal discs with minutely plumose white hairs, medium-lengthed on lateral parts, short on mediobasal parts of terga 2–4, minute and inconspicuous elsewhere. Tergal marginal zones 2–4 with distinct, continuous white hair bands covering entire zone length, 2–3 becoming sparser medially, 4 evenly dense. Prepygidial fimbria white laterally, whitish medially; pygidial fimbria whitish-golden (Fig. 197). Head (Figs. 195–196). 1.2 times broader than long. Galea shagreened, apex weakly pointed. Labral process trapezoidal, apex distinctly narrower than base, shiny, basal half transversely striated. Clypeus slightly protuberant apically, slightly convex, very smooth and shiny except for narrow basolateral shagreenation, strongly punctured, distance between punctures 1–2 puncture diameters, a narrow impunctate midline is weakly indicated (Fig. 195). Flagellomere 1 slightly longer than 2+3, 2 slightly shorter than 3. Frons and upper half of paraocular area longitudinally striated, impunctate. Facial foveae broad, slightly tapering below, extending from level of upper end of lateral ocellus to upper end of antennal socket, 0.7 times as broad as antennocular distance, distance from lateral ocellus 1 ocellus diameter (Figs. 195–196). Ocelloccipital distance 1 ocellus diameter. Vertex slightly carinate, almost rounded (Fig. 196). Mesosoma (Fig. 196). Pronotum with slightly elevated dorsolateral angle, without lateral carina. Mesonotum shiny, moderately shagreened, very shallowly and imperceptibly punctured, distance between punctures 1–2 puncture diameters. Scutellum smooth and shiny medially, shagreened posteriorly, with densely punctate midline (Fig. 196). Mesepisternum finely alveolate, impunctate. Propodeal corbicula finely reticulate, impunctate. Posterolateral part of propodeum finely rugose-alveolate. Propodeal triangle similar, becoming more rugose mediobasally. Inner side of hind femur rounded, not carinate. Hind pretarsal claw distinctly bidentate. Recurrent vein 1 meets submarginal cell 2 at its distal third. Nervulus strongly antefurcal (Fig. 198). Metasoma (Fig. 197). Tergal discs shagreened, finely and very shallowly punctured, distance between punctures 1–2 puncture diameters. Tergal disc 1 strongly shagreened and matt, 2 and especially 3–4 more weakly so, somewhat shiny. Tergal marginal zones weakly depressed; marginal zone 1 shagreened basally, weakly shagreened apically; 2–4 weakly shagreened basally, smooth apically. Pygidial plate with elevated margin, without elevated medial area. Male (Fig. 199). Body length: 5.5 mm. Colour. Head Black. Clypeus and lower half of paraocular area black (Fig. 200). Frons and upper half of paraocular area with slight metallic luster. Anterior side of flagellomeres 3–11 orange. Mesonotum, scutellum and metanotum black with weak metallic luster (Fig. 201). Legs moderate to dark brown, tarsi brown basally, reddishbrown apically. Wings hyaline, veins brown, stigma brownish-yellow medially (Fig. 199). Tergal discs brown to black, tergal marginal zones reddish-yellow basally, yellow apically (Fig. 202). Pubescence. Head and dorsal part of mesosoma with white to yellowish, minutely plumose hairs (Figs. 199– 201). Mesepisternum and propodeum with long white plumose hairs. Legs with short white to whitish hairs (Fig. 199). Tergal hair as in female. Terminal fringe white (Fig. 202). Head (Figs. 200–201). 1.2 times broader than long. Labral process trapezoidal, shiny, apical margin weakly emarginate. Clypeus slightly protuberant apically, almost flat medially, very smooth and shiny, strongly punctured, distance between punctures 2 puncture diameters, without impunctate midline (Figs. 199–200). Flagellomere 1 about as long as 2+3, 2 slightly shorter than 3. Frons and upper half of paraocular area longitudinally striated, weakly punctate, puncture density increasing dorsolaterally. Ocelloccipital distance 1 ocellus diameter. Vertex moderately carinate (Fig. 201). Genal area rounded posteriorly. Mesosoma (Fig. 201). Pronotum without or with slightly elevated dorsolateral angle, without lateral carina. Mesonotum and scutellum weakly shiny, distinctly shagreened, anterior half of mesonotum sparsely punctured, distance between punctures 2–4 puncture diameters (Fig. 201). Rest of mesosoma as in female. Metasoma (Fig. 202). Similar to female. Genitalia and hidden sterna (Fig. 203). Genital capsule more or less rounded. Dorsal gonocoxite lobe developed, weakly pointed. Gonostyli spatulate, apical half gradually broadening, apex rounded. Penis valves broad basally, basal part flanked by dorsal lamella, strongly tapering apically (Fig. 203). Sternum 8 simple, columnar, slightly narrowing apically, apical process slightly broadened. Diagnosis. Andrena asluji belongs to a group of unclassified desert-dwelling Andrena characterised by a shiny, flattened female clypeus, smooth scutellum, usually reddish terga, and characteristic genitalia. This group includes A. gafsensis Wood, A. helouanensis Friese, A. maidaqi Scheuchl & Gusenleitner and A. tenebricorpus Wood. The female of Andrena asluji differs from these species in the reddish tergal colouration (completely dark in A. tenebricorpus), shorter fovea (reaching level of lower end of antennal socket in A. helouanensis and A. maidaqi), ocelloccipital distance equalling 1 ocellus diameter (0.3 in A. gafsensis, 1.5 in A. maidaqi, 1.5–2 in A. helouanensis), shagreened mesonotum (completely smooth in A. helouanensis, smooth centrally in A. gafsensis, A. maidaqi and A. tenebricorpus), shagreened, almost impunctate terga (smooth and distinctly punctured in A. gafsensis, A. helouanensis and A. tenebricorpus), and brightly coloured scopa and terminal fringe (brown in A. helouanensis and A. tenebricorpus). The male of A. asluji differs from all these species (the male of A. tenebricorpus is unknown) in the fully dark clypeus. Additionally, flagellomere 1 is as long as 2+3 (shorter than 2+ 3 in A. helouanensis and A. maidaqi), the mesonotum and terga are shagreened (smooth in A. helouanensis), the dorsal gonocoxite lobes are straight (directed sideways in A. helouanensis and A. maidaqi), and the gonostyli are unmodified (blade strongly broadened in A. gafsensis and A. maidaqi). Andrena asluji also resembles A. (incertae sedis) aegyptiaca Friese, but differs in the simple-haired scopa and the more shagreened mesonotum and terga. Distribution: Sandy habitats in southern Israel. Flight period: February–March. Flower records: Brassicaceae: Eremobium aegyptiacum; Maresia sp.; Thymelaeaceae: Thymelaea hirsuta. Holotype: ISRAEL: Holot Mash’abbim Nature Reserve [Holot Mash’abbim], 30.999ºN 34.758ºE, 18.ii.2022, G. Pisanty, pan trap, ♀ (SMNHTAU:384650). Paratypes: ISRAEL: Holot Mash’abbim Nature Reserve, 30.999ºN 34.757ºE, 10.iii.2017, G. Pisanty, on Brassicaceae (1♀); 17.iii.2017, G. Pisanty, on Brassicaceae (1♀); [Holot Mash’abbim], 14.ii.2012, G. Pisanty, partly on Eremobium aegyptiacum (4♂); 17.iii.2012, G. Pisanty, on Thymelaea hirsuta (1♂); 30.999ºN 34.7578ºE, 18.ii.2022, G. Pisanty, pan traps (2♂); 30.999ºN 34.758ºE, 18.ii.2022, G. Pisanty, pan traps (2♀); Mishor Rotem, 21.ii.1966, M. Weichselfish, on Maresia (1♂) (OLML, RMNH, SMNHTAU). Etymology. Named after Bir ‘Asluj (Be’er Mash’abim), a historical landmark located 2 km north of the type locality. The species epithet is an adjective., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 82-85, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826
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24. Andrena (Melandrena) grandilabris Perez 1903
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Andrena grandilabris ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Melandrena) grandilabris Pérez, 1903 Distribution: Turkey. Material examined (A. elmaria Gusenleitner): ISRAEL: Eilon [Elon], 27.iii.1946, H. Bytinski-Salz (1♀); Jerusalem, 27.ii.1940, H. Bytinski-Salz (1♀); 5.iii.1940, H. Bytinski-Salz (1♂);? Jerusalem [Jer], 27.ii.1940 (1♂); Kiryat Anavim [Qiryat ‘Anawim], 5.iii.1937, on Sinapis (1♂) (SMNHTAU). Remarks. Israeli specimens identified by Warncke as A. grandilabris (Warncke 1969) actually belong to the related A. elmaria Gusenleitner, which is common in Israel.A similar situation may exist with the record of A. grandilabris from Cyprus (Varnava et al. 2020), which remains to be confirmed., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 102, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Perez, J. (1903) Especes nouvelles de Melliferes (palearctiques). Proces-verbaux des seances de la Societe Linneenne de Bordeaux, 58, LXXVIII - XCIII + CCVIII - CCXXXVI.","Warncke, K. (1969) A contribution to the knowledge of the genus Andrena (Apoidea) in Israel. Israel Journal of Entomology, 4, 377 - 408.","Varnava, A. I., Roberts, S. P., Michez, D., Ascher, J. S., Petanidou, T., Dimitriou, S., Devalez, J., Pittara, M. & Stavrinides, M. C. (2020) The wild bees (Hymenoptera, Apoidea) of the island of Cyprus. ZooKeys, 924, 1 - 114. https: // doi. org / 10.3897 / zookeys. 924.38328"]}
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25. Andrena (Micrandrena) protuber Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Andrena protuber ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Micrandrena) protuber Pisanty sp. nov. (Figs. 127–136) Female (Fig. 127). Body length: 6 mm. Colour. Body and legs dark brown to black (Fig. 127). Anterior side of flagellomeres 3–10 dark brown. Wings hyaline, veins dark brown, stigma brown. Tergal marginal zones light brown to yellowish (Fig. 134). Pubescence. Clypeus with medium-lengthed whitish hairs, apical margin with long brown hairs (Figs. 129– 130). Outer half of paraocular area with short to medium black hairs. Area around antennal sockets with both whitish and black medium-lengthed hairs. Facial foveae brown. Vertex with medium brownish hairs. Genal area with short black hair anteriodorsally, medium whitish hair posteroventrally. Mesonotum, scutellum and metanotum with short to medium whitish to brown hair (Figs. 127, 132). Mesepisternum with long white hair (Fig. 127). Propodeal corbicula incomplete, posterodorsal fringe with long white plumose hair, corbicular surface with medium-lengthed weakly plumose white hair. Leg hair white to brown. Flocculus incomplete, white. Tibial scopal hair weakly plumose, greyish-white (Fig. 127). Tergal discs with sparse, minute inconspicuous white hair centrally, short white hair laterally. Tergal marginal zones 2–4 with distinct narrow bands of short white hair on apical half, interrupted on 2–3, almost continuous on 4. Terminal fringe light brown (Fig. 134). Head (Figs. 129, 130, 132). 1.1 times broader than long. Mandible bidentate. Galea shiny, shallowly, finely shagreened. Labral process broad and short, trapezoidal, smooth and shiny except near base, apical margin blunt to slightly concave. Clypeus moderately protuberant, strongly convex, strongly shagreened basolaterally, smooth and shiny centrally, coarsely punctured, distance between punctures 1–2 puncture diameters, apical half with weakly indicated impunctate midline, apical margin of clypeus laterally thickened and densely longitudinally striated (Figs. 129–130). Supraclypeal and paraocular areas and frons finely longitudinally striated and moderately to finely punctured, punctation finer dorsally. Flagellomere 1 about as long as 2+3, 2 as long as 3 or slightly shorter. Facial foveae linear and narrow, extending from level of lower end of lateral ocellus almost to lower end of antennal socket, weakly tapering downwards, distinctly separated from compound eye, 0.4 times as broad as antennocular distance (Figs. 129, 132). Distance of fovea from lateral ocellus about 1.5 ocellus diameters. Ocelloccipital distance about 0.7 ocellus diameter. Vertex weakly to moderately carinate (Fig. 132). Mesosoma (Fig. 132). Dorsolateral angle of pronotum not elevated, pronotum not carinate. Mesonotum finely and uniformly shagreened, weakly shiny, finely, shallowly and irregularly punctured, distance between punctures 1–3 puncture diameters. Scutellum very shiny and more weakly shagreened, similarly punctured (Fig. 132). Mesepisternum and propodeal corbicula finely reticulate, shallowly obliquely punctured. Posterolateral part of propodeum finely reticulate, area close to triangle very finely, shallowly rugose. Propodeal triangle broad, equilateral, delineated by distinct carina, mediobasal part distinctly radially rugose, apicolateral part finely reticulate (Fig. 132). Hind tibial spur distinctly curved apically. Hind pretarsal claw bidentate. Nervulus antefurcal. Submarginal crossvein 1 meets marginal cell 2–5 vein widths from stigma. Metasoma (Fig. 134). Tergal disc 1 smooth, 2–4 shallowly shagreened to almost smooth basally, smooth apically, tergal punctation fine to very fine, distance between punctures 1–2 puncture diameters, apical ¼ of discs mostly impunctate, punctation gradually finer on discs 3–4. Tergal marginal zones shallowly shagreened to smooth, occasionally with fine punctures. Male (Fig. 128). Body length: 5.5–6 mm. Colour. Head and mesosoma black (Fig. 128). Anterior side of flagellomeres 2–11 brown. Legs dark brown to black. Wings hyaline, veins dark brown, stigma brown. Metasoma brown to black. Tergal marginal zones light brown to yellowish (Fig. 136). Pubescence. Clypeus hair medium to long, two-coloured, white medioapically, black laterally, black to mixed black and white mediobasally (Figs. 128, 131). Paraocular area and frons with short to long black hairs. Area around antennal sockets with black and white, medium to long hairs. Central part of vertex with long erect whitish hairs. Lateral part of vertex and anteriodorsal part of genal area with medium black hairs. Posteroventral part of genal area with white hairs. Mesonotum, scutellum and metanotum with sparse, medium-lengthed erect white to yellowish-white hair (Figs. 128, 133). Mesepisternum mostly with long white hairs, dorsal part also with few black hairs (Fig. 128). Propodeum with long white hairs. Legs with white to brownish hairs. Tergal discs with sparse, minute inconspicuous white hair centrally, short white hair laterally. Tergal marginal zones 2–4 with weak, narrow bands of short white hair on apical half, broadly interrupted on 2–3, narrowly interrupted on 4 (Fig. 136). Head (Figs. 131, 133). 1.1 times broader than long. Labral process broad and short, trapezoidal to rectangular, smooth and shiny, apical margin blunt to slightly concave. Clypeus convex, moderately protuberant, strongly shagreened basolaterally, smooth and shiny centrally, strongly punctured, distance between punctures 1–2 puncture diameters, without impunctate midline (Fig. 131). Supraclypeal and paraocular areas and frons finely longitudinally striated and moderately to finely punctured, punctation finer dorsally. Flagellomere 1 about as long as 3, longer than 2. Ocelloccipital distance about 1 ocellus diameter. Vertex moderately carinate, dorsoposterior margin of genal area often slightly carinate (Fig. 133). Mesosoma (Fig. 133). Mesonotum and scutellum finely and uniformly shagreened, weakly shiny, punctation fine and extremely shallow, often imperceptible, distance between punctures 1–3 puncture diameters (Fig. 133). Nervulus strongly antefurcal to almost interstitial (Fig. 128). Rest of mesosoma as in female. Metasoma (Fig. 136). Tergal discs shiny, basal part weakly to strongly shagreened, apical part more or less smooth, punctation fine to very fine, distance between punctures 1.5–2 puncture diameters, apical margin of discs sparsely punctured to almost impunctate. Tergal marginal zones weakly depressed, shagreened to smooth, occasionally with sparse, very fine punctures. Genitalia and hidden sterna (Fig. 135). Dorsal gonocoxite lobes weakly developed, broadly rounded. Gonostylus blades flattened, tongue-shaped. Penis valves of moderate width, basal part slightly tapering apically (Fig. 135). Sternum 8 columnar, apical process broadened, apical margin blunt. Diagnosis. Andrena protuber is distinguished from most other Micrandrena by the narrower head (Figs. 129, 131) and weaker sculpturing of the mesonotum and propodeal triangle (Figs. 132, 133), which are more typical of Aciandrena, Fuscandrena and Graecandrena, and the Andrena fumida species group (subgenus Fumandrena sensu Warncke); and by the unusual female clypeus, reminiscent of A. (Euandrena) symphyti, which is protuberant, centrally smooth, and laterally longitudinally striated especially at the apical margin (Figs. 129, 130). In the weakly sculptured mesonotum, the males resemble A. immaculata Warncke but can easily be separated by the genital capsule which lacks lateral extensions on the penis valves. Distribution: Northern Israel. Likely present also in Lebanon and Syria. Flight period: March–May. Flower records: Cupressaceae: Juniperus drupacea. The species was collected from pan traps in two localities where plants of Symphytum brachycalyx (Boraginaceae) and/or individuals of Andrena symphyti Schmiedeknecht were also present. It also shares the same protuberant clypeus of the larger Andrena symphyti, which is presumably associated with enhanced mouthparts that enable females to extract pollen and nectar from Boraginaceae flowers. We therefore hypothesize that the species is a Boraginaceae specialist, by analogy to A. symphyti. Holotype: ISRAEL: Mount Meron [Har Meron], 33.000°N 35.3927°E, 4.iv.2017, G. Pisanty, pan trap, ♀ (SMNHTAU:270289). Paratypes: ISRAEL: Mount Hermon [Har Hermon], 1642 m, 33.2996°N 35.7677°E, 16.iv.2022, G. Pisanty, pan trap (1♂); 19.v.2022, G. Pisanty, pan traps (2♀); 1644 m, 33.2991°N 35.7667°E, 16.iv.2022, G. Pisanty, pan trap (1♂); 1645 m, 33.2994°N 35.7675°E, 16.iv.2021, G. Pisanty (5♂); 1649 m, 33.2992°N 35.7677°E, 16.iv.2022, G. Pisanty, on Juniperus drupacea (4♂); 1650 m, 33.299°N 35.769°E, 7.iv.2021, G. Pisanty (3♂); Mount Meron [Har Meron], 33.000°N 35.3927°E, 4.iv.2017, G. Pisanty, pan trap (1♀); 1000 m, 1.iv.2012,A. Freidberg (2♂); 1000 m, 32°59.7’N 35°24.7’E, 14.iv.2011, L. Friedman (1♂); Nahal Keziv, Montfort, 33°02.6’N 35°13.3’E, 4.iii.2010, L. Friedman (1♀, 1♂); Sasa, 20.iv.2015, O. Winberger (1♀); Ziv’on, 1 km SW, 33.019°N 35.407°E, 5.iv.2016, G. Pisanty, pan trap (1♂) (OLML, RMNH, SMNHTAU, TJW). Etymology. protuber = Latin for “lump in front”, referring to the protruding clypeus in the female sex. The species epithet is a noun in apposition., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 56-59, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826
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26. Andrena (incertae sedis) janthinoides Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (incertae sedis) janthinoides Pisanty sp. nov. (Figs. 222–229) Female (Fig. 222). Body length: 5.5–6 mm. Colour. Body and legs dark brown to black (Fig. 222). Anterior side of flagellomeres 4–10 gradually becoming reddish apically. Wings hyaline, veins dark brown, stigma dark brown peripherally, golden medially (Fig. 222). Tergal marginal zones light brown basally, whitish to yellowish apically (Fig. 225). Pubescence. Body mostly with relatively sparse and short, white to yellowish plumose hair (Fig. 222). Clypeus and supraclypeal area with very sparse and short white hair. Paraocular area and scape with moderately dense, short to medium white hair. Frons with sparse, medium-lengthed white hair (Fig. 223). Upper 1/2–2/3 of facial fovea brownish, lower part whitish (Figs. 223–224). Vertex with short to medium, white to yellowish hair. Genal area with short yellowish hair dorsally, short to medium white hair ventrally. Mesonotum with sparse, short to medium, white to yellowish hair, denser peripherally. Metanotum and posterior margin of scutellum with medium-lengthed white to yellowish hair (Fig. 224). Mesepisternum with long white hair. Propodeal corbicula incomplete, dorsoposterior fringe with long white hair; corbicular surface with few long, white simple hairs. Leg hair mostly white; scopal hairs simple, white; flocculus complete, white (Fig. 222). Tergal discs laterally with sparse short white hair; basal part of tergal disc 1 with sparse short white hair; apical part hairless; the following tergal discs gradually with sparse, minute white hair. Tergal marginal zones 1–4 with dense narrow bands of white hair originating from apical half of marginal zone, slightly extending onto following tergal disc, broadly interrupted on tergum 1, gradually more continuous on 2–3, fully continuous on 4. Prepygidial fimbria white laterally, whitish-golden medially; pygidial fimbria whitish-golden (Fig. 225). Head (Figs. 223–224). 1.3 times broader than long. Mandible bidentate. Galea superficially shagreened except on inner basal part. Labral process rectangular to weakly trapezoidal, much broader than long. Clypeus slightly convex, flattened medially, smooth except on basal margin, sparsely but distinctly punctured, distance between punctures 1–2 puncture diameters, without impunctate midline (Fig. 223). Flagellomere 1 slightly longer than 2+3, 2 shorter than 3. Frons longitudinally striated. Facial foveae moderately broad, strongly tapering downwards, very shallow on upper part, extending from level of middle–lower end of lateral ocellus to base of clypeus, 0.7 times as broad as antennocular distance (Figs. 223–224). Distance of fovea from lateral ocellus about 1 ocellus diameter. Ocelloccipital distance 1.2 ocellus diameters. Vertex weakly carinate (Fig. 224). Genal area as broad as compound eye. Mesosoma (Fig. 224). Pronotum without elevated dorsolateral angle or lateral carina. Mesonotum shiny, finely shagreened, finely, sparsely and superficially punctured, distance between punctures 1–3 puncture diameters. Scutellum similar, punctures sparser and obscurer (Fig. 224). Mesepisternum finely alveolate. Propodeal corbicula finely reticulate. Posterior part of propodeum finely alveolate, triangle weakly demarcated, apical 2/3 of triangle slightly shinier compared to flanking regions, basal 1/3 very superficially and finely rugose-areolate (Fig. 224). Hind pretarsal claw bidentate. Recurrent vein 1 meets submarginal cell 2 at 1/2–2/3 of its length. Submarginal crossvein 1 meets marginal cell 2–3 vein widths from stigma. Nervulus antefurcal (Fig. 222). Metasoma (Fig. 225). Tergal discs shiny, basal 2/3–3/4 finely shagreened, apical part smooth, shagreenation of tergum 4 more superficial; punctation mostly absent, very fine and sparse punctures can be noticed mostly on smooth apical areas. Tergal marginal zones very superficially shagreened to smooth, impunctate, 1 narrow and not depressed, the following gradually broader and more depressed. Pygidial plate without medial elevated zone. Male (Fig. 226). Body length: 5–5.5 mm. Colour. Anterior side of flagellomeres 4–10 brown to reddish-brown (Fig. 226). Rest of body similar to female (clypeus and paraocular area black). Pubescence. Apical 2/3 of clypeus with dense fringe of medium-lengthed white hairs, extending below clypeus to about 1/2 clypeus length. Paraocular area and scape with moderately dense, medium white to yellowish hair. Frons with sparse, medium-lengthed white to yellowish hair (Figs. 226–227). Vertex with short to long, white to yellowish hair. Genal area with short yellowish hair dorsally, gradually long white hair ventrally. Mesonotum with sparse, medium to long, white to yellowish hair, denser peripherally. Metanotum and posterior half of scutellum with long white to yellowish hair (Fig. 228). Mesepisternum and propodeum with long white hair (Figs. 226, 228). Legs mostly with short to medium, white to yellowish hair (Fig. 226). Tergal discs laterally with moderately dense short white hair; medially with sparse short white hair. Tergal marginal zones 1–4 with weak narrow bands of white hair originating from apical half of marginal zone, interrupted on 1–3, almost continuous on 4. Head (Figs. 227–228). 1.3 times broader than long. Labral process rectangular to weakly trapezoidal, much broader than long. Clypeus slightly convex, flattened medially, smooth except on basal margin, strongly and densely punctured, distance between punctures 0.5–1 puncture diameters, without impunctate midline (Fig. 227). Flagellomere 1 about as long as 2+3, 2 shorter than 3. Frons longitudinally striated. Ocelloccipital distance 1.3 ocellus diameters. Vertex weakly carinate (Fig. 228). Genal area about as broad as compound eye, posterior margin rounded, not pointed or carinate. Mesosoma (Fig. 228). Similar to female, but mesonotal punctation extremely shallow and obscure, propodeal triangle more distinctly rugose basally (Fig. 228). Metasoma. Similar to female. Genitalia and hidden sterna (Fig. 229). Dorsal gonocoxite lobe developed, moderately pointed. Gonostylus suddenly broadened apically, blade shaped as right triangle, apex weakly pointed. Penis valves moderately broad basally, strongly tapering apically (Fig. 229). Sternum 8 simple, columnar, apical process broadened, triangular. Diagnosis. Andrena janthinoides is closely related to A. janthina Warncke. The two species belong to a unique, unclassified lineage of Andrena, which is related to Fuscandrena and Micrandrena (Pisanty et al. 2022). Andrena janthinoides is easily distinguished from A. janthina in its smaller size and apically smooth terga (uniformly shagreened in A. janthina) (Fig. 225). The female also differs in the trapezoidal labral process (arched in A. janthina) and almost completely smooth and flat clypeus, reminiscent of A. (Ulandrena) dauma Warncke (shagreened basally and transversely arched in A. janthina) (Fig. 223). Distribution: Israel. Most specimens were collected in the Mediterranean habitat regions of northern and central Israel. However, a single male record exists from the extreme desert of the Arava Valley (Hazeva), which could be a labeling error. Flight period: February–April. Flower records: Apiaceae: Ferula communis; Rosaceae: Prunus dulcis. Holotype: ISRAEL: Forest of the Martyrs [Ya’ar Kedoshim], 27.iii.2014, N. Shamir, on Ferula communis, ♀ (SMNHTAU:152552). Paratypes: ISRAEL: Beit Jimal [Bet Jimal], 3.iv.1988, I. Yarom (1♀); Beit Nir [Bet Nir], 11.iii.2018, T. Roth, pan traps (2♀); Forest of the Martyrs [Ya’ar Kedoshim], 2.iii.2014, N. Shamir, pan traps (1♀); 26.ii.2017, Y. Farago, pan traps (1♀, 1♂); 8.iii.2017, Y. Farago (1♀); Hazeva, 4 km W, 11–17.iv.1988, R. Leys (1♂); Kfar Menahem [Kefar Menahem], 1.iii.2008, Y. Mandelik, pan traps (1♀); 2.iii.2008, U. Roll, pan traps (2♀, 1♂); 2.iii.2008, Y. Mandelik, on Prunus dulcis (1♀); Lakhish, 19.iii.2013, T. Shapira, pan traps (1♀); 8.iv.2013, T. Shapira, pan traps (1♀); Mount Meron [Har Meron], 4 km E, 9.iv.1988, R. Leys (2♂); Nahariya [Nahariyya], 10 km E, 9.iv.1988, R. Leys (5♂); Rehan Forest, south to Rangers’ House, 11.iv.2007, L. Friedman (1♀); Sheikh Ali, 20 km E Qiryat Gat, 17.iii.1990, R. Kasher (1♂); Tal Shahar, 2.iv.2010, G. Pisanty, pan traps (1♀); Valley of Elah [Emeq Ha’ela], 10.iv.2006, W. Mahagna (1♀) (OLML, RMNH, SMNHTAU, TJW). Etymology. From janthina + oides, i.e. similar to A. janthina. The species epithet is an adjective., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 91-93, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Pisanty, G., Richter, R., Martin, T., Dettman, J. & Cardinal, S. (2022) Molecular phylogeny, historical biogeography and revised classifcation of andrenine bees (Hymenoptera: Andrenidae). Molecular Phylogenetics and Evolution, 170, 107151."]}
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27. Andrena (Micrandrena) cedricola Wood 2020
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Andrena cedricola ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Micrandrena) cedricola Wood, 2020 Distribution: High altitudes in Israel (first record), Lebanon, Syria and Turkey (first record) (Wood et al. 2020a). Flight period: March–May (Wood et al. 2020a). Flower records: Brassicaceae: Brassica sp. (Wood et al. 2020a), Peltaria angustifolia. Material examined: HOLOTYPE: LEBANON: Hadath el Jebbe, Border of the Cedar forest, 1646 m, 13.v.2019, M. Boustani (♀) (RBINS); non-type material: ISRAEL: Hermon Nature Reserve [Hermon NR], 1508 m, 300 m N lower parking lot, 33.294°N 35.760°E, 28.v.2019, L. Friedman (2♀); Hermon Nature Reserve, Biq’at Man, 1450 m, 33.292°N 35.751°E, 29.iv.2022, G. Pisanty, on Peltaria angustifolia (2♀); Merom Golan, 1000 m, 23.iv.1997, R. Kasher (1♀); Mount Hermon [Har Hermon], 1480 m, 33.292°N 35.7595°E, 7.iv.2021, G. Pisanty, pan trap (1♂); 1600 m, 23.v.1998, A. Freidberg (1♀); 18.v.2009, L. Friedman (1♀); 1620 m, 33.300°N 35.767°E, 11.v.2020, G. Pisanty (1♂); 1644 m, 33.2992°N 35.7670°E, 16.iv.2022, G. Pisanty, pan trap (1♂); 1645 m, 33.2994°N 35.7675°E, 16.iv.2021, G. Pisanty, pan traps (3♂) and sweeping (1♂); [Har Hermon], Nahal Guveta, 1410 m, 33.285°N 35.763°E, 11.v.2020, G. Pisanty, on Peltaria angustifolia (10♀, 4♂); [Hermon], 1640–1675 m, 33.298–299°N 35.767–770°E, 19.v.2022, G. Pisanty, on Brassicaceae (1♀); Mount Meron, 1100 m, 13.iv.1988, I. Yarom (2♀, 1♂); [Har Meron], 1100 m, 17.iv.2000, A. Freidberg (3♂); Neve Ativ, 16 km NE Qiryat-Shmona, 1000 m, 18.iv.1990, R. Kasher (1♀); Nimrod Castle [Qala’at Nemrod], 6.v.1987, A. Shlagman (2♀, 1♂); SYRIA: Camp Faouar [Faouar], 11.iii.2001, J. Plass (1♂); TURKEY: Hakkari, 18 km NW Yüksekova, 1800 m, 13.vi.1981, K. Warncke (2♀); Hakkari, Suvari Halil-Pass, 2300 m, 14.vi.1981, K. Warncke (6♀); Tanin-Tanin-Pass, 1900 m, 3.vi.1980, M. Schwarz (1♀) (OLML, SMNHTAU, TJW)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 46, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Wood, T. J., Boustani, M. & Rasmont, P. (2020 a) A revision of the Andrena (Hymenoptera: Andrenidae) of Lebanon with the description of six new species. Annales de la Societe Entomologique de France, 56, 279 - 312. https: // doi. org / 10.1080 / 00379271.2020.1794960"]}
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28. Andrena (Euandrena) vulpecula Kriechbaumer 1873
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Andrena vulpecula ,Hymenoptera ,Taxonomy - Abstract
Andrena (Euandrena) vulpecula Kriechbaumer, 1873 Distribution: Algeria, Croatia, France, Greece, Italy, Morocco, Portugal, Slovenia, Spain, Tunisia (Gusenleitner & Schwarz 2002). Material examined (A. rufitibialis Warncke species complex): ISRAEL: Binyamina [Benjamina], 1.xii.1946, H. Bytinski-Salz, on Colchicum (2♀) (SMNHTAU). Remarks. Israeli specimens identified as by Warncke A. vulpecula (Warncke 1969) actually belong to the species complex of Andrena rufitibialis Warncke. The easternmost verified records of A. vulpecula are from Greece., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 101, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Kriechbaumer, J. (1873) Hymenopterologische Beitrage. III. Verhandlungen der Zoologisch-Botanischen Gesellschaft in Wien, 23, 49 - 68.","Gusenleitner, F. & Schwarz, M. (2002) Weltweite Checkliste der Bienengattung Andrena mit Bemerkungen und Erganzungen zu palaarktischen Arten (Hymenoptera, Apidae, Andreninae, Andrena). Entomofauna, Supplement 10, 1 - 1280.","Warncke, K. (1969) A contribution to the knowledge of the genus Andrena (Apoidea) in Israel. Israel Journal of Entomology, 4, 377 - 408."]}
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29. Andrena (Melandrena) pyrozonata Friese 1921
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy ,Andrena pyrozonata - Abstract
Andrena (Melandrena) pyrozonata Friese, 1921 Distribution: Cyprus, Israel, Turkey. Likely present also in Lebanon and Syria. Flight period: March–April. Flower records: Fagaceae: Quercus infectoria (Mavromoustakis 1958); Sapindaceae: Acer monspessulanum. Material examined: HOLOTYPE: TURKEY: Kahramanmaraş, Kayabaşı [Kayabaschi], 8.vii.1913, F. Tölg (♀) (ZMHB); PARATYPE (A. perapedica Mavromoustakis): CYPRUS: Pera Pedi, 4.iv.1952, Mavromoustakis (1♀) (SMNHTAU); non-type material: ISRAEL: Montfort [Monfort], 17.iii.1983, A. Freidberg (1♂); Mount Hermon [Har Hermon], 1640 m, 33.300°N 35.7675°E, 7.iv.2021, G. Pisanty, sweeping (1♀); 1644 m, 33.2992°N 35.7670°E, 16.iv.2022, G. Pisanty, pan trap (1♀); 1649 m, 33.2993°N 35.7679°E, 16.iv.2021, G. Pisanty, on Acer monspessulanum (2♀); Nahal Kziv [Nahal Keziv], 5.iii.2008, L. Friedman (1♂) (SMNHTAU). Remarks. This species was formerly classified in the polyphyletic group known as Poliandrena (now a synoynm of Ulandrena, Pisanty el. 2022). We now reclassify it under Melandrena, as it is closely related morphologically to A. (Melandrena) elmaria Gusenleitner, and the barcode sequences of these two species cluster together with A. (Melandrena) nigroaenea (Kirby) in phylogenetic analyses of barcode sequences., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 46, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Friese, H. (1921) Apidae. In: Fahringer, J. & Friese, H., Eine Hymenopteren-Ausbeute aus dem Amanusgebirge (Kleinasien und Nord-Syrien, sudl. Armenien). Archiv fur Naturgeschichte, Abteilung A, 87 (3), pp. 150 - 176.","Mavromoustakis, G. A. (1958) New bees of the genera Andrena and Nomada from the island Cyprus (Hymenoptera: Apoidea), part II. Beitrage zur Entomologie, 8 (1 - 2), 212 - 219."]}
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30. Andrena (Chlorandrena) danini Pisanty & Scheuchl 2016
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Andrena danini ,Hymenoptera ,Taxonomy - Abstract
Andrena (Chlorandrena) danini Pisanty & Scheuchl, 2016 (Figs. 58–62, 64–65) Male (Fig. 58). Body length: 7–7.5 mm. Colour. Head, mesosoma and legs black (Fig. 58). Apical 1/4–1/3 of clypeus usually yellow, at least centrally; paraocular area black (Fig. 59). Anterior side of flagellomeres 2–11 brown. Wings hyaline, veins and stigma brown. Metasoma dark brown to black; tergal marginal zones yellowish-brown, sometimes reddish (Fig. 61). Pubescence. Head and mesosoma with medium to long white hair, especially dense and long on genal area, mesepisternum and fore coxa (Figs. 58–60). Femora and tibiae with white hair, tarsi with white to golden hair (Fig. 58). Tergal discs with moderately dense white hair, relatively long on tergum 1, gradually shorter on following terga, longer on lateral parts of terga. Tergal marginal zones with similar hair, denser on lateral parts, not forming distinct hair bands (Fig. 61). Head (Figs. 59–60). 1.2 times broader than long. Labral process broader than long, trapezoidal, smooth and shiny, apical margin distinctly emarginate. Clypeus convex, very weakly protuberant, shagreened on basolateral margin, elsewhere smooth and shiny, punctation strong and dense, distance between punctures 1 puncture diameter, without impunctate midline (Fig. 59). Flagellomere 1 twice as long as 2, slightly longer than 3. Frons strongly longitudinally striated, interspersed with fine punctures. Ocelloccipital distance 1.2 ocellus diameters. Vertex strongly carinate, posterodorsal margin of genal area slightly carinate (Fig. 60). Mesosoma (Fig. 60). Dorsolateral angle of pronotum not elevated, pronotum not carinate. Mesonotum and scutellum shiny, distinctly shagreened peripherally, weakly shagreened to smooth centrally, strongly punctured, distance between punctures 0.5–1.5 puncture diameters (Fig. 60). Mesepisternum and anterolateral part of propodeum strongly and densely obliquely punctured. Posterolateral part of propodeum finely alveolate, finely and irregularly rugose. Propodeal triangle delineated by weak carina, very finely rugose basally, very finely rugose to alveolate apically. Nervulus interstitial to antefurcal. Metasoma (Fig. 61). Tergal discs shiny, 1 shagreened to smooth, 2–4 shagreened basally, weakly shagreened to smooth apically, disc 1 with strong, coarse crater-like punctures, the following discs gradually more shallowly punctured, distance between punctures 1–2 puncture diameters. Tergal marginal zones broad, moderately depressed, impunctate, finely shagreened except near apex, 2–4 occupying 0.4–0.5 of tergum length centrally. Genitalia and hidden sterna (Figs. 62, 64–65). Dorsal gonocoxite lobes adjoined along medial genital axis, strongly developed, rounded apically. Gonostyli very elongate, blades flattened, leaf-shaped, apex weakly to strongly pointed. Basal 1/3 of penis valves of moderate, uniform width, central 1/3 tapering apically, apical 1/3 narrow (Fig. 62). Sternum 8 columnar, without lateral extensions, slightly broadened medially, apical half densely, uniformly hairy on ventral side, elsewhere mostly hairless, apical process slightly broadened, blunt-ended (Figs. 64–65). Diagnosis. The males of A. danini very closely resemble those of A. cinereophila Warncke, and Warncke regarded them as a subspecies of the latter, named Andrena cinereophila antelica nomen nudum. The true identity of these specimens was only made possible with the advent of DNA barcoding (Table 2). Andrena danini males are distinguished from A. cinereophila by the smaller yellow apical area on the clypeus (covering half of clypeus in A. cinereophila), the more or less evenly, finely rugose propodeal triangle (basal margin more or less radially rugose, more strongly sculpted than apical part in A. cinereophila), the centrally smooth tergal discs 2–3, with distinct crater-like punctures (smooth to shagreened, crater-like punctures absent or weakly present only laterally in A. cinereophila), the more elongate genital capsule, and the straight, adjoined, apically rounded dorsal gonocoxite lobes (diverging outwards, more pointed apically in A. cinereophila) (Figs. 62–63). Distribution: Israel (Pisanty et al. 2016); newly recorded from Jordan, Syria, Turkey and the West Bank, in arid to semi-arid habitats. In Israel, A. danini is present in the central region and the northern Negev, as well as the Jordan Valley, but it is apparently absent from the more mesic-habitat regions of the Carmel, Galilee, northern Golan and Mount Hermon. Flight period: February–April, occasionally into May in Turkey (one handwritten record apparently from July, possibly erroneous). Flower records: Asteraceae: Calendula sp., Crepis sancta, Geropogon hybridus, Leontodon tuberosus; Brassicaceae: Sinapis sp.; Geraniaceae: Geranium sp.; Linaceae: Linum pubescens. Material examined: HOLOTYPE: ISRAEL: Lakhish, 3 km NE, 31.578°N 34.870°E, 19.ii.2016, G. Pisanty (♀) (SMNHTAU:234232); PARATYPES: ISRAEL: Besor Stream [Bsor W.], 4.iii.1985, E. Shney-Dor (1♀); Canada Park, 31.836°N 35.000°E, 18.iii.2016, G. Pisanty (1♀); Hartuv [Har.Tuv], 22.ii.1955, student (1♀); Jerusalem, 2.? vii.1940, H. Bytinski-Salz (1♀); Lakhish, 6.iii.2013, T. Shapira, pan traps (2♀); 20.iii.2013, T. Shapira, pan traps (2♀); 8.iv.2013, T. Shapira, pan trap (1♀); 13.iv.2013, T. Shapira, pan traps (2♀); 3 km NE, 31.575°N 34.870°E, 4.iii.2016, G. Pisanty, partly from pan traps (3♀); 11.iii.2016, G. Pisanty (1♀); 19.iii.2016, G. Pisanty, pan traps (2♀); 31.578°N 34.870°E, 19.ii.2016, G. Pisanty (1♀); Netiv HaLamed-Heh [Netiv Halamed He], 2 km WNW, 31.694°N 34.96°E, 26.ii.2009, G. Pisanty (1♀) (ES, OLML, SMNHTAU); non-type material: ISRAEL: Beit Guvrin [Beit Govrin], 28.iii.2010, G. Pisanty (6♀); Beit Nir, 28.iii.2010, G. Pisanty (1♀); 11.iii.2018, T. Roth, on Crepis sancta (1♀) and Linum pubescens (1♀); Degania [Deganya], 23.ii.1942, Y. Palmoni (1♂) (A. c. antelica paratype label); Gal’on, 4.iv.2018, T. Roth, on Geropogon hybridus (1♀); Gilat Research Center, fallow field, 31.3372ºN 34.6633ºE, 2.iii.2022, G. Pisanty, pan traps (2♂); Har’el, 21.ii.2020, K. Levy, pan trap (1♂); Horbat Sheqofa, 252 m, 31.5775°N 34.871°E, 15.iii.2021, G. Pisanty, pan traps (3♀, 7♂); Jerusalem, Mt. Scopus, 22.ii.1946 (1♂) (A. c. antelica paratype label); 15.iii.1946, on Calendula, Geranium and Sinapis (6♂) (A. c. antelica holotype / paratype labels); Jerusalem env., 28.iii.1988, R. Leys (1♂); Kfar Menahem [Kefar Menahem], 6.ii.2010, G. Pisanty, on Leontodon tuberosus (1♂); Lakhish, 21.ii.2013, T. Shapira, pan trap (1♂); 3 km NE, 31.578°N 34.870°E, 19.ii.2016, G. Pisanty (2♂); [Lachish], 18.ii.2020, K. Levy, pan trap (1♀) and T. Roth, on Crepis sancta (1♂); 4.iii.2020, K. Levy, pan trap (1♂); 8.iii.2020, K. Levy, pan trap (1♂); 8.iii.2020, T. Roth, on Crepis sancta (1♂); Ma’agar Yeroham [Yerucham Lake], 15.iv.1997, A. Maklakov (1♀); Mikveh Israel [Miqwe Israel], 10.iii.1919, H. Bytinski-Salz (1♂) (A. c. antelica paratype label); Nahal Arugot [N.Arugot], 2.iii.1981, S. Kronenberg (1♀); Nahal Poleg [Birquat Ramadan], 13.iii.1940, H. Bytinski-Salz (1♂) (A. c. antelica paratype label); Negba, 31.iii.2021, Y. Halevi (1♀, 1♂); Netiv HaLamed-Heh [Netiv Halamed He], 2 km WNW, 31.694°N 34.96°E, 26.ii.2009, G. Pisanty, pan trap (1♂); Tell es-Safi [Tel Zafit], 7.iii.2018, T. Roth, pan traps (2♀); JORDAN: Irbid, Saham, 25.iv.2003, I. Pljushtch (1♀); SYRIA: Jabbul-See, SE Aleppo, 300 m, 19.iv.1992, K. Warncke (1♀); Maaloula [Maalula], 15.iv.1992, M. Kraus (1♀); TURKEY: Urfa, Ceylanpınar, 25.iv.1976, K. Warncke (1♂); Urfa, 20 km SE Harran, 23.v.1983, K. Warncke (1♀); WEST BANK: Har Brakha [Berakha], 1 km S, ‘Amassa Spring, 595 m, 6.iii.2015, L. Friedman (1♂); Maskiot [Maskiyyot], Rt. 578, Wadi Halat Mahmud el-‘Ali, – 75 m, 32°19’18’’N 35°29’52’’E, 27.ii.2020, L. Friedman (1♀); Wadi Ahmar, nr. Yarden, 32°01’N 35°30’E, 15.iii.2005, I. Zonstein (1♂); Wadi al-Far’a [Wadi Faria], 19.ii.1974, A. Freidberg (1♂) (A. c. antelica paratype label); Wadi Qelt [Nahal Perat], south-facing slope, 28.ii.2007, L. Friedman (1♂) (OLML, RMNH, SMNHTAU, TJW).
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31. Andrena (Euandrena) symphyti Schmiedeknecht 1883
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy ,Andrena symphyti - Abstract
Andrena (Euandrena) symphyti Schmiedeknecht, 1883 Distribution: South and Central Europe, Caucasus, Near East (Gusenleitner & Schwarz 2002; Scheuchl & Willner 2016). Newly recorded from Syria and northern Israel, which is apparently its southernmost distributional limit. A single record exists from Israel’s central coastal plain (Kfar Azar), but this could be a labeling error. Flight period: February–May (Israel), April–June (Central Europe, Scheuchl & Willner 2016). Flower records: Oligolectic on Boraginaceae: Cerinthe,? Nonea, Onosma, Symphytum (Scheuchl & Willner 2016). Material examined: HOLOTYPE (A. symphyti furcata): TURKEY: Kahramanmaraş, Kayabaşı [Kayabaschi], 8.vii.1913, F. Tölg (♀) (ZMHB); non-type material: ISRAEL: Hermon Nature Reserve, Har Shezif, 1447 m, 33.286°N 35.7524°E, 16.iv.2022, G. Pisanty, pan traps (1♀, 4♂); Kfar Azar [Kefar Azar], 2.ii.1955, student (1♀); Montfort, Nahal Kziv [Nahal Keziv], 28.ii.2018, G. Pisanty (1♂); Mount Hermon [Har Hermon], 1642 m, 33.2996°N 35.7677°E, 19.v.2022, G. Pisanty, pan trap (1♀); Mount Meron [Har Meron], 5.iv.2016, G. Pisanty (4♀); 33.000°N 35.3927°E, 4.iv.2017, G. Pisanty, pan traps (28♀, 7m + 8♀ stylopised), sweeping (4♀) and on Symphytum brachycalix (10♀, 4♂ + 3♀ stylopised); 1000 m, 1.iv.2012, L. Friedman (1♂); 17.iv.2012, L. Friedman (1♂); 1100 m, 32º59.7’N 35º24.7’E, 14.iv.2011, A. Freidberg (1♂); [Meron], 23.iv.1973, D. Furth (1♀); SYRIA: Slanfah [Slenfe], 1200 m, 19.iv.1986, K.M. Guichard (1♀) (ES, NHMUK, OLML, SMNHTAU, TJW). Remarks. COI barcode sequences show a 2.4–2.7% difference between Israeli vs. Central European populations of A. symphyti. We employ here a broad species concept of A. symphyti, as there is no clear ‘break point’ between populations separated by Warncke as A. symphyti in Europe and A. symphyti furcata Friese in Turkey and the Caucasus (see map in Gusenleitner & Schwarz 2002). We prefer to consider this a continuum of variation across this range until demonstrated otherwise., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 45, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Gusenleitner, F. & Schwarz, M. (2002) Weltweite Checkliste der Bienengattung Andrena mit Bemerkungen und Erganzungen zu palaarktischen Arten (Hymenoptera, Apidae, Andreninae, Andrena). Entomofauna, Supplement 10, 1 - 1280.","Scheuchl, E. & Willner, W. (2016) Taschenlexikon der Wildbienen Mitteleuropas: Alle Arten im Portrat. Quelle & Meyer Verlag, Wiebelsheim, 917 pp."]}
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32. Andrena (Hoplandrena) najadana Warncke 1975
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Andrena najadana ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Hoplandrena) najadana Warncke, 1975 Distribution: High altitudes (1300–1700 m) in Israel (first record) and Turkey. Likely present also in Lebanon and Syria. Flight period: April (Warncke 1974c). Flower records: Sapindaceae: Acer monspessulanum. Material examined: HOLOTYPE: TURKEY: Akseki / Taurus, 1300 m, 25.iv.1973, K. Warncke (♂) (OLML); non-type material: ISRAEL: Mount Hermon [Har Hermon], 1649 m, 33.2993°N 35.7679°E, 16.iv.2021, G. Pisanty, on Acer monspessulanum (1♀, 2♂); 1650 m, 33.2993°N 35.7678°E, 16.iv.2022, G. Pisanty, on Acer monspessulanum (3♀) (SMNHTAU)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 46, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Warncke, K. (1975) Die Sandbienen der Turkei (Hymenoptera, Apoidea, Andrena), Teil B. Beschreibungen der neuen Andrena - Arten bzw. Unterarten. Mitteilungen der Munchner Entomologischen Gesellschaft, 65, 29 - 102.","Warncke, K. (1974 c) Die Sandbienen der Turkei (Hymenoptera, Apoidea, Andrena), Teil A. Mitteilungen der Munchner Entomologischen Gesellschaft, 64, 81 - 116."]}
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33. Andrena (Holandrena) forsterella Osytshnjuk 1978
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena forsterella ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Holandrena) forsterella Osytshnjuk, 1978 Distribution: Azerbaijan, Bulgaria, Croatia, Cyprus, Greece, Iran, Italy, Lebanon, Macedonia, Turkey (Gusenleitner & Schwarz 2002; Wood et al. 2020a); newly recorded from Israel. Flight period: May–June (Israel), up to August in more northern latitudes (Schönitzer et al. 1995). Flower records: None. Material examined: ISRAEL: Beit Uziel [Bet Uzi’el], 27.v.2011, N. Meltzer (1♂); Jerusalem, Mt. Scopus, 26.v.1940 (1♀); Revadim, 28.v.2011, A. Golan (1♂); 30.v.2011, A. Golan (1♂); 4.vi.2011, A. Golan (1♂); 7.vi.2011, A. Golan (1♂); Merom Golan, 33°08’N 35°46’E, 1.vi.2008, I. Gerlitz (1♀) (SMNHTAU). Remarks. This species has often been confused with Andrena wilhelmi Schuberth, which has an earlier flight period, and is also present in Israel (Pisanty et al. 2018)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 45-46, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Osytshnjuk, A. Z., Panfilov, D. V. & Ponomareva, A. A. (1978) Apoidea. In: Tobias, V. I. (Ed.), Species of Insects of the European Region of the USSR. Vol. 3. Hymenoptera. Academy of Sciences of the USSR, Zoological Institute, St. Petersburg, pp. 279 - 519.","Gusenleitner, F. & Schwarz, M. (2002) Weltweite Checkliste der Bienengattung Andrena mit Bemerkungen und Erganzungen zu palaarktischen Arten (Hymenoptera, Apidae, Andreninae, Andrena). Entomofauna, Supplement 10, 1 - 1280.","Wood, T. J., Boustani, M. & Rasmont, P. (2020 a) A revision of the Andrena (Hymenoptera: Andrenidae) of Lebanon with the description of six new species. Annales de la Societe Entomologique de France, 56, 279 - 312. https: // doi. org / 10.1080 / 00379271.2020.1794960","Schonitzer, K., Grunwaldt, W., Gusenleitner, F., Osytshnjuk, A. Z. & Schuberth, J. (1995) Klarung von Andrena forsterella, mit Hinweisen zu den anderen Arten der Andrena labialis - Gruppe (Hymenoptera, Apoidea, Andrenidae). Linzer Biologische Beitrage, 27 (2), 823 - 850.","Pisanty, G., Scheuchl, E. & Dorchin, N. (2018) Taxonomic revision of the subgenus Andrena (Poecilandrena) (Hymenoptera: Andrenidae) in Israel and the Levant. Zootaxa, 4374 (2), 151 - 188. https: // doi. org / 10.11646 / zootaxa. 4374.2.1"]}
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34. Andrena (Poecilandrena) mediterranea Pisanty & Scheuchl 2016, stat. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrena mediterranea ,Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Poecilandrena) mediterranea Pisanty & Scheuchl, 2016 stat. nov. Andrena sphecodimorpha mediterranea Pisanty & Scheuchl, 2016 Distribution: North and central Israel, Jordan, Lebanon, Syria, West Bank (Pisanty et al. 2018, Wood et al. 2020a). Flight period: February–May (Pisanty et al. 2018; Wood et al. 2020a). Flower records: Amaryllidaceae: Allium trifoliatum; Apiaceae: Scandix verna; Asteraceae: Leontodon tuberosus; Brassicaceae: Diplotaxis erucoides, Erysimum spp., Thlaspi spp.; Euphorbiaceae: Euphorbia sp.; Iridaceae: Moraea sisyrinchium; Plantaginaceae: Veronica syriaca; Rosaceae: Pyrus syriaca (Pisanty et al. 2016, 2018; Wood et al. 2020a; new records). Material examined: HOLOTYPE: ISRAEL: Lakhish, 2 km E, 31.5562°N 34.869°E, 4.iii.2016, G. Pisanty, pan trap (♀) (SMNHTAU:235320); PARATYPES: see Pisanty et al. 2016; new records: ISRAEL: Har’el, 21.ii.2020, T. Roth, on Leontodon tuberosus (1); Hermon Nature Reserve, 1670 m, 33.299°N 35.769°E, 28.iv.2021, A. Dorchin (1♀); Hermon Nature Reserve [Hermon Nat. Res.], 1467 m, 33.292°N 35.7505°E, 29.iv.2022, G. Pisanty, on Euphorbia (1♀); [Hermon], Biq’at Man, 1450 m, 33.292°N 35.751°E, 29.iv.2022, G. Pisanty (2♀); Meron Junction, 20.iii.1995, on Pyrus syriaca (2♀); Mount Gilboa [Hare Gilboa’], Har Avinadav, 32°28’N 35°26’E, 22.iii.2012, L. Friedman (1♀); Mount Hermon [Har Hermon], 1420 m, 33.2855°N 35.763°E, 7.iv.2021, G. Pisanty, pan traps (7♀, 1♂); 1480 m, 33.292°N 35.760°E, 11.v.2020, G. Pisanty, pan traps (1♀); 33.2922°N 35.7595°E, 7.iv.2021, G. Pisanty, pan traps (2♂); 1540 m, 33.296°N 35.763°E, 7.iv.2021, G. Pisanty, pan traps (2♀); 1610 m, 33.300°N 35.767°E, 7.iv.2021, G. Pisanty, pan traps (6♀); 1640 m, 33.300°N 35.7675°E, 7.iv.2021, G. Pisanty, sweeping (2♂); 1642 m, 33.2992°N 35.7668°E, 19.v.2022, G. Pisanty, pan traps (1♀, 1♂); 33.2996°N 35.7677°E, 19.v.2022, G. Pisanty, pan trap (1♀); 1644 m, 33.2991°N 35.7667°E, 16.iv.2022, G. Pisanty, pan traps (2♀, 3♂); 33.2992°N 35.7670°E, 16.iv.2022, G. Pisanty, pan trap (1♂); 1645 m, 33.2994°N 35.7675°E, 16.iv.2021, G. Pisanty, pan traps (4♂) and sweeping (2♀); [Har Hermon], Nahal Guveta, 1410 m, 33.285°N 35.763°E, 11.v.2020, G. Pisanty, pan traps (2♀); [Hermon], 1640–1675 m, 33.298–299°N 35.767–770°E, 19.v.2022, G. Pisanty, on Erysimum (1♀); Odem Forest Nature Reserve [Ya’ar Odem N.R.], 1.iii.2018, G. Pisanty (5♀, 4♂); [Ya’ar Odem NR], 33.186°N 35.7356°E, 27.ii.2020, G. Pisanty, pan traps (5♂); 3.205°N 35.736°E, 27.iv.2020, G. Pisanty, pan traps (4♀); 33.206°N 35.736°E, 27.ii.2020, G. Pisanty, pan traps (2♂); WEST BANK: Har ‘ Eval, 750–800 m, 29.iii.2021, L. Friedman (1♂) (SMNHTAU). Remarks. Molecular data of the nominate A. sphecodimorpha Hedicke and of A. hybrida Warncke is still unavailable to us. However, both sexes of A. mediterranea are well separated from these species by several traits (shagreenation, hair colouration, integumental colouration, see Pisanty et al. 2016). According to our improved understanding of species limits within Andrena and specifically Poecilandrena, such differences are clearly sufficient to demarcate different species., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 64-65, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Pisanty, G., Scheuchl, E. & Dorchin, N. (2016) Eight new species of Andrena Fabricius (Hymenoptera: Apoidea: Andrenidae) from Israel - a Mediterranean hotspot for wild bees. Zootaxa, 4189 (3), 485 - 515. https: // doi. org / 10.11646 / zootaxa. 4189.3.3","Pisanty, G., Scheuchl, E. & Dorchin, N. (2018) Taxonomic revision of the subgenus Andrena (Poecilandrena) (Hymenoptera: Andrenidae) in Israel and the Levant. Zootaxa, 4374 (2), 151 - 188. https: // doi. org / 10.11646 / zootaxa. 4374.2.1","Wood, T. J., Boustani, M. & Rasmont, P. (2020 a) A revision of the Andrena (Hymenoptera: Andrenidae) of Lebanon with the description of six new species. Annales de la Societe Entomologique de France, 56, 279 - 312. https: // doi. org / 10.1080 / 00379271.2020.1794960"]}
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35. Andrena (Chlorandrena) tadauchii Gusenleitner 1998
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Andrena tadauchii ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Chlorandrena) tadauchii Gusenleitner, 1998 Andrena edentula Wood, 2020 syn. nov. Distribution: Israel, Syria, Turkey, West Bank. Likely present also in Lebanon. Flight period: February–May. Flower records: Asteraceae: Crepis aspera, Glebionis coronaria, Picris spp., Rhagadiolus stellatus; Brassicaceae: Sinapis arvensis. Material examined: HOLOTYPE (A. edentula): SYRIA: occ. Al-Nasrah [An Nasrah] env., 8.iv.2005, J. Saki (♂) (OLML); non-type material: ISRAEL: Aderet, 24.iii.2010, G. Pisanty, pan trap (1♀); Banias, 18.iv.1992, R. Kasher (1♀); [Panyas], 430 m, 15.iii.2011, 33°14.850’N 35°41.674’E, A. Freidberg (1♂); Beit Guvrin [Beit Govrin], 28.iii.2010, G. Pisanty, pan traps (4♀); [Bet-Govrin, 20 km S Hebron], 17.iii.1990, R. Kasher (1♂); Beit Nir, 28.iii.2010, G. Pisanty, pan traps (2♀); 25.iii.2018, T. Roth, on Picris (1♀); Beit Oren [Bet Oren], 1.5 km S, 18.iv.2015, 32.715 35.01, G. Pisanty (1♀); Giv’at Gad [Sheich-Ali, 20 km E Qiryat-Gat], 17.iii.1990, R. Kasher (1♂); Haifa University, 10.iv.1988, I. Yarom (1♀, 1♂); Har Gilo, 11.iv.1990, R. Kasher (1♂); Holot Nizzanim Nature Reserve, Nahal Evtah, 25.ii.2009, A. Freidberg (1♂); Horbat Sheqofa, 252 m, 15.iii.2021, 31.5775°N 34.8709°E, G. Pisanty, pan trap (1♂); Hurshat Tal, 13.iii.1996, R. Kasher (1♂); Jerusalem, 19.iii.1955, J. Wahrman (1♀); Jerusalem [Yerushalayim], 13.iv.2014, I. Arar, on Crepis aspera (1♀) and Sinapis arvensis (1♂); 27.ii.2015, T. Jumah (1♂); Kfar Giladi [Kefar Gil’adi], 1.iv.1997, R. Kasher (1♀, 1♂); 12.iv.1997, R. Kasher (1♀); 24.iv.1997, R. Kasher (1♀); Kfar Menahem [Kefar Menahem], 19.ii.2010, G. Pisanty (1♀); Lakhish, 3 km NE, 26.ii.2016, 31.578°N 34.870°E, G. Pisanty (1♂); 4.iii.2016, 31.575°N 34.870°E, G. Pisanty (2♂); 11.iii.2016, 31.575°N 34.870°E, G. Pisanty (1♀); Majdal Shams, 1100 m, 27.iv.2020, 33.262°N 35.755°E, G. Pisanty (1♀); Malkia [Malkiyya], 27.iv.2014, O. Winberger, pan traps (2♀); Matzuva [Mazuva], 18.iii.1951, J. Wahrman (1♀); Meirav [Hare Gilboa’, Merav], Har Avinadav, 420 m, 20.iii.2012, 32º28’N 35º26’E, L. Friedman (1♂); Merom Golan, 3.iv.1997, R. Kasher (5♀, 4♂); 20.iv.1997, R. Kasher (3♂); 23.iv.1997, R. Kasher (2♂); Mount Carmel, 2 km SE Haifa University, 24.iii.1990, A. Dafni (2♀, 6♂); Mount Carmel [Har Shana (Carmel)], 24.iii.1989, J. Kugler (1♀); Mount Hermon, 23.iv.1973, H. Bytinski-Salz (4♂) (A. holophila paratype labels); [Har Hermon], 1640 m, 7.iv.2021, 33.300°N 35.7675°E, G. Pisanty, sweeping (2♂); 1644 m, 33.2992°N 35.7670°E, 16.iv.2022, G. Pisanty, pan trap (1♂); 1645 m, 16.iv.2021, 33.2994°N 35.7675°E, G. Pisanty, pan traps (2♂) and sweeping (1♂); [Sheh], 26.v.1972, M. Tintpulver (1♀); Mount Meron [Har Meron], 5.iv.2016, 32.9945°N 35.415°E, G. Pisanty (1♂); Nahal Alexander, 30.iii.2021, K. Levy (1♀); Nahal ‘ Iyyon, 430 m, HaTanur Waterfall, 33º16.064’N 35º34.500’E, 15.iii.2011, E. Morgulis (1♂); Nahal ‘ Iyyon Nature Reserve, haTanur [Tanur], 15.iii.1975, F. Kaplan (1♂); Nahal Sa’ar, 30.iii.1997, R. Kasher (1♀, 5♂); Nimrod Castle [Qala’at Nemrod], 6.v.1987, A. Shlagman (1♀); Road 869, 1.65 km W Daliyyot Junction, 428 m, 11.iv.2019, 32.892°N 35.760°E, A. Dorchin, O. Halbershtat & Y. Mersman (1♀); Snir, Hermon Field Study Center, 5.iii.1996, R. Kasher (1♀); 31.iii.1996, R. Kasher, on Rhagadiolus stellatus (1♀); 4.iv.1996, R. Kasher (1♀); 6.iv.1996, R. Kasher (1♀); 27.iii.1997, R. Kasher (1♀); 3.iv.1997, R. Kasher (1♀); WEST BANK: Mevo Horon, 24.ii.2010, G. Pisanty, on Glebionis coronaria (2♂); SYRIA: Stausee, 10 km SW Homs, 500 m, 15.iv.1992, M. Kraus & K. Warncke (2♂) (OLML, SMNHTAU). Remarks. Andrena tadauchii was originally described from a single female as A. humilis prunella Warncke, 1975, but this name was preoccupied by an unrelated taxon described from Afghanistan (nec A. prunella Warncke, 1974). Due to the scarcity of material, Warncke could not associate the two sexes together, and labeled the males as A. holophila nomen nudum, but died before publishing them. Gusenleitner (1998) renamed A. h. prunella as A. tadauchii, associated the sexes together and described the male. In the Warncke collection, only the female was available for study until recently, when specimens used to describe the male were discovered in an unmarked box. Andrena tadauchii is part of the humilis -group within the subgenus Chlorandrena, though its male is highly unusual for this group as its sternum 8 is noticeably enlarged and resembles members of the rhenana -group. As a result, Wood et al. 2020a misdiagnosed A. edentula as an undescribed taxon belonging to the rhenana -group, and not the male of tadauchii. After inspection of the missing material, the two taxa are synonymised, and male material has been integrated into the Warncke collection proper., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 36-37, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Gusenleitner, F. (1998) Neue westpalaarktische Andrena - Arten (Hymenoptera: Apidae: Andreninae). Entomofauna, 19 (6), 109 - 144.","Warncke, K. (1975) Die Sandbienen der Turkei (Hymenoptera, Apoidea, Andrena), Teil B. Beschreibungen der neuen Andrena - Arten bzw. Unterarten. Mitteilungen der Munchner Entomologischen Gesellschaft, 65, 29 - 102.","Wood, T. J., Boustani, M. & Rasmont, P. (2020 a) A revision of the Andrena (Hymenoptera: Andrenidae) of Lebanon with the description of six new species. Annales de la Societe Entomologique de France, 56, 279 - 312. https: // doi. org / 10.1080 / 00379271.2020.1794960"]}
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36. Andrena (Euandrena) rufula Schmiedeknecht 1883
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Andrena rufula ,Hymenoptera ,Taxonomy - Abstract
Andrena (Euandrena) rufula Schmiedeknecht, 1883 Distribution: South and Central Europe, Turkey and Lebanon (Gusenleitner & Schwarz 2002; Scheuchl & Willner 2016; Wood et al. 2020a). Newly recorded from Israel and Syria. Flight period: March–April, up to May in Central Europe (Scheuchl & Willner 2016). Flower records: Rosaceae: Crataegus spp., Prunus dulcis, Prunus spinosa, Pyrus syriaca; Salicaceae: Salix spp.; Sapindaceae: Acer spp. (Scheuchl & Willner 2016 and new records). Material examined: ISRAEL: Hermon Nature Reserve [Hermon Reserve], 21.iv.2012, G. Pisanty, on Prunus dulcis (1♀); Meron Junction [Meron JNC.], 20.iii.1995, on Pyrus syriaca (3♀); Mount Hermon [Har Hermon], 1640 m, 33.300°N 35.7675°E, 7.iv.2021, G. Pisanty, sweeping (1♀); 1649 m, 33.2993°N 35.7679°E, 7.iv.2021, G. Pisanty, on Acer monspessulanum (2♀, 1♂); 16.iv.2021, G. Pisanty, on Acer monspessulanum (33♀, 2♂ + 4♀ stylopised); 1650 m, 33.2993°N 35.7678°E, 16.iv.2022, G. Pisanty, on Acer monspessulanum (2♀); [Hermon], 1641 m, 33.2993°N 35.7670°E, 16.iv.2022, G. Pisanty, on Prunus dulcis (2♀); SYRIA: Bloudan [Bludan], 57 km NW Damascus, 2000 m, 24.iv.1992, K. Warncke (8♀, 1♂); Maaloula [Maalula], 60 km NE Damaskus, 1400 m, 14.iv.1992, K. Warncke (1♀); TURKEY: Akseki, 17.iv.1974, K. Warncke (2♂) (OLML, SMNHTAU)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 43, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Gusenleitner, F. & Schwarz, M. (2002) Weltweite Checkliste der Bienengattung Andrena mit Bemerkungen und Erganzungen zu palaarktischen Arten (Hymenoptera, Apidae, Andreninae, Andrena). Entomofauna, Supplement 10, 1 - 1280.","Scheuchl, E. & Willner, W. (2016) Taschenlexikon der Wildbienen Mitteleuropas: Alle Arten im Portrat. Quelle & Meyer Verlag, Wiebelsheim, 917 pp.","Wood, T. J., Boustani, M. & Rasmont, P. (2020 a) A revision of the Andrena (Hymenoptera: Andrenidae) of Lebanon with the description of six new species. Annales de la Societe Entomologique de France, 56, 279 - 312. https: // doi. org / 10.1080 / 00379271.2020.1794960"]}
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37. Andrena (Truncandrena) seitzi Alfken 1935
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Andrena seitzi ,Hymenoptera ,Taxonomy - Abstract
Andrena (Truncandrena) seitzi Alfken, 1935 Distribution: Turkey. Material examined (A. urfanella Scheuchl & Hazir): ISRAEL: Dafna [Daphne], 20.ii.19??, H. BytinskiSalz (2♂); Mikveh Israel [Mikwe Israel, Mikweh Israel], 10.iii.19??, H. Bytinski-Salz (3♂); Nir Am, 14.iii.19??, H. Bytinski-Salz (5♂); Rosh Pina, 19.iii.1943, H. Bytinski-Salz (1♂); Zikhron Ya’akov [Sichron Yaacov], 16.iv.19??, H. Bytinski-Salz (1♂) (SMNHTAU). Remarks. Israeli male specimens assumed by Warncke to be A. seitzi (Warncke 1969) were reidentified as A. urfanella Scheuchl & Hazir., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 103, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Warncke, K. (1969) A contribution to the knowledge of the genus Andrena (Apoidea) in Israel. Israel Journal of Entomology, 4, 377 - 408."]}
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38. Andrena (Micrandrena) decollata Warncke 1974
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Andrena decollata ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Micrandrena) decollata Warncke, 1974 Distribution: Mediterraean coastline of Algeria, Lybia and Tunisia (Gusenleitner & Schwarz 2002); newly recorded from the coastal plain of Israel. Flight period: January–April. Flower records: Brassicaceae; Boraginaceae: Alkanna strigosa. Material examined: ISRAEL: Binyamina, 26.i.1976, A. Freidberg (1♂); Gan Sorek [Gan Soreq], Give’at Humera, 4.ii.2020, L. Friedman (1♂); Gvulot [Gevulot], 14.iii.1987, E. Shney-Dor (1♀); Holon [Hulon], 18.i.1954, L. Fishelsohn (1♂); Kadima [Qadima], 5.iii.1990, R. Kasher, on Alkanna strigosa (1♀); 6.iv.2015, I. Eliakim (1♂); Mikveh Israel [Mikve Israel], 5.iii.1946 (1♀); Nahal Alexander, 27.ii.2020, K. Levy, pan trap (4♀); 16.iii.2020, K. Levy, pan trap (2♀); Nitzanim [Nizzanim], 17.ii.2005, A. Freidberg (3♂); Nizzanim Nature Reserve, 25.ii.2009, A. Freidberg (2♂) and L. Friedman (1♀, 2♂); Rehovot, ii.1934, Hecht (3♀, 1♂); 9.ii.1942, H. Bytinski-Salz (3♀); [R.Gh] (possibly Ramat Gan or Ramat Chen), 3.ii.1940 (1♀); 6.ii.1940 (1♀); Tel Aviv, 17.iii.1940, H. Bytinski-Salz (1♀);?. iii.1940, H. Bytinski-Salz (1♂); Tel Aviv, Ramat Aviv, 32.130°N 34.801°E, 9.ii.2015, G. Pisanty, pan traps (2♀, 2♂); 1.iv.2017, G. Pisanty, partly on Brassicaceae (2♂); Zur Moshe, 27.iv.2015, I. Eliakim (1♀, 1♂); TUNISIA: Hammamet env., 15.iii.1996, K. Deneš (2♀) (OLML, RMNH, SMNHTAU, TJW). Remarks. Israeli specimens of A. decollata were erroneously identified by Warncke as A. longibarbis Pérez (Warncke 1969). Pisanty et al. (2018) considered them a distinct, undescribed species related to A. decollata. However, upon examination of more material, we see no reason to separate them from the north African material of A. decollata., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 47-48, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Gusenleitner, F. & Schwarz, M. (2002) Weltweite Checkliste der Bienengattung Andrena mit Bemerkungen und Erganzungen zu palaarktischen Arten (Hymenoptera, Apidae, Andreninae, Andrena). Entomofauna, Supplement 10, 1 - 1280.","Warncke, K. (1969) A contribution to the knowledge of the genus Andrena (Apoidea) in Israel. Israel Journal of Entomology, 4, 377 - 408.","Pisanty, G., Scheuchl, E. & Dorchin, N. (2018) Taxonomic revision of the subgenus Andrena (Poecilandrena) (Hymenoptera: Andrenidae) in Israel and the Levant. Zootaxa, 4374 (2), 151 - 188. https: // doi. org / 10.11646 / zootaxa. 4374.2.1"]}
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39. Andrena (Suandrena) mirna Warncke 1969
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Andrena mirna ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Suandrena) mirna Warncke, 1969 Andrena cyanomicans mirna Warncke, 1969 Distribution: Iran, Southern Israel, Jordan, Lebanon, West Bank (Warncke 1969; Khodaparast & Monfared 2012; Wood et al. 2020a). Flight period: January–April. Flower records: Brassicaceae: Erucaria rostrata, Sinapis alba: Fabaceae: Retama raetam. Material examined: PARATYPES: ISRAEL [Palestine]: Yeruham [Bir Rechme], 13.iii.[no year], H. Bytinski-Salz (1♀, 1♂); WEST BANK [Palestine]: Jericho, 25.i.2941, H. Bytinski-Salz (1♀) (SMNHTAU); non-type material: ISRAEL: Arad, 570 m, 31°15.346’N 35°11.958’E, 7.iii.2010, A. Freidberg (5♂); Avdat, 21.iii.1985, A. Freidberg (1♂); [Avedat], 16.iii.1988, A. Freidberg (1♀); Be’erotaim Bridge, 26.ii.1968, D. Gerling (1♂); Ein Gedi, 23.iii.1958, I. Kugler (1♂); Har Horesha, Rt. 171, 930 m, 2.iv.2014, A. Freidberg (1♀) & L. Friedman (1♂); Hatira, Negev, Israel, 8.ii.2002, E. Groner (1♀); Hazeva Field School, 30°43’N 35°15’E, 12.iii.1998, E. Ashkenazi, Malaise trap (2♂); Irus Yeroham Nature Reserve [Irus Yeroham NR], 31.021°N 34.9725°E, 13.ii.2022, G. Pisanty, on Retama raetam (1♂); Lehavim, 31.365°N 34.830°E, 28.i.2015, G. Pisanty, pan traps (2♀, 1♂); Lehavim Junction [LehavimJun.], 5.iv.1988, F. Kaplan (1♀); Masua, 12.iii.1985, A. Hefetz (1♀); near Mount Tzaror, Hatira, Negev, Israel, 8.ii.2002, E. Groner (1♀); 14.ii.2002, E. Groner (1♀); Nahal Aqrabim, 9.iii.1991, R. Kasher (1♂); Nahal Loz [Nahal Lotz], 21.ii.2014, G. Pisanty (2♀); Nahal Zin [Zin 2], 6.iii.2007, Y. Hollander (1♂); Netiv HaGdud, 22.ii.1985, A. Hefetz (2♀); Park ha-Les Nature Reserve [Park ha-Les NR], 31.2575ºN 34.5965ºE, 19.iii.2022, G. Pisanty, pan trap (1♀); Sa’ad, 31.469°N 34.528°E, 21.i.2015, G. Pisanty, on Brassicaceae (1♀, 1♂); Sde Boker, 17.iii.1970, Gasith (2♀); [Sede Boqer], 21.iii.1985, I. Yarom (1♂); 17.iii.1999, L. Friedman (1♂); [Sede Boqer], route 90, 30°51’N 34°46’E, 12.iv.2009, O.Avlas (1♀); 3 km N [Sede-Boqer], 19.ii.1995, R. Kasher (2♀, 3♂); Shivta, 13.iii.1977, A. Freidberg (1♀); Yeruham [Kfar-Jerucham], 24.iii.1959, I. Kugler (3♀, 2♂); WEST BANK: Almog, 20.i.1990, R. Kasher, on Erucaria rostrata (1♀); [Almog, 10 km S Jericho], – 350 m, 3.ii.1990, R. Kasher, on Erucaria rostrata (2♀); Nahal Gilgal, 6.i.1973, Yehiam (1♀); Petza’el [Fza’el, 23 km SE Nablus], – 300 m, R. Kasher, on Sinapis alba (1♀, 1♂); [Peza’el], – 200 m, 32°2’57’’N 35°26’7’’E, 18.ii.2020, G. Pisanty (1♀) (SMNHTAU). Remarks. The taxonomy of the subgenus Suandrena is complex, and has had several different and variable interpretations through time (e.g. Warncke 1974a; Dylewska 1983; Gusenleitner & Schwarz 2002; Kratochwil et al. 2014; Kratochwil 2021). Warncke separated A. cyanomicans Pérez into three subspecies, the nominate in Iberia, A. c. fratella Warncke from northwestern Africa, and A. c. mirna from the southern Levant. Previous authors have stated that A. mirna is a valid species, and have used it as such (Khodaparast & Monfared 2012; Kratochwil et al. 2014; Kratochwil 2021). We agree with this interpretation; female A. mirna differ from the nominate form in the black terga which lack metallic reflections (terga with metallic blue-green reflections in A. cyanomicans), scopa almost entirely black with only a few slightly lightened hairs ventrally (scopa almost entirely orange with dark brown hairs dorsobasally at basitibial plate in A. cyanomicans), and pubescence of mesosoma generally whitish-greyish, dorsally with some intermixed black hairs (pubescence of mesosoma generally light brown, dorsally with abundant intermixed black hairs in A. cyanomicans). Males can be separated by their whitish mesosomal pubescence (light brown in A. cyanomicans) and more strongly produced hairbands (hairbands very weakly produced in A. cyanomicans). Due to the geographic separation and the lack of introgression between these forms, A. mirna should be treated as distinct from A. cyanomicans. Other material examined (A. cyanomicans Pérez): LECTOTYPE: SPAIN: Barcelona [Barcelone] (♂) (MNHN); non-type material: SPAIN: Albaricoques env., 25.iii.2014, P. Bogusch (2♀, 1♂); Altea, 10 km N Benidorm, 15.iv.1982 (1♂); Barcelona, Villaneueva y Geltru, 30.ix.1964, D. Drenth (1♀, 2♂); Murcia, Los Alcazares, 11.ix.1977, J.A. Veenstra (1♀, 3♂) (OLML, RMNH, TJW).
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- 2022
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40. Andrena (incertae sedis) ornithogali Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
- Author
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Insecta ,Arthropoda ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (incertae sedis) ornithogali Pisanty & Wood sp. nov. (Figs. 230–241) Female (Fig. 233). Body length: 7–9 mm. Colour. Body black (Fig. 233). Flagellomeres 3–10 greyish-black anteriorly. Legs dark brown to black. Wings hyaline, veins and stigma dark brown (Fig. 233). Tergal marginal zones brown (Fig. 232). Pubescence. Head and dorsal side of mesosoma mostly with moderately dense, medium-lengthed, minutely plumose hair (Figs. 230, 231, 233). Clypeus, frons, paraocular and supraclypeal areas with black hair; some specimens with few bright hairs around antennal sockets (Figs. 230, 233). Facial foveae black in anterior view, somewhat brownish in dorsal view (Figs. 230–231). Vertex with mixed, short to long, black and brownish-white erect hairs. Genal area with short black hairs. Mesonotum, scutellum and metanotum with medium-lengthed white to brownish hairs interspersed with shorter, thinner black hairs (Figs. 231, 233). Mesepisternum with long black hairs, becoming more plumose towards ventral area. Propodeal corbicula incomplete, posterodorsal fringe with long, strongly plumose black hairs, corbicular surface with sparse, medium-lengthed, simple golden hairs. Foreleg and midleg femora and outer side of tibiae with black hairs; inner side of tibiae and all tarsi with brown to golden hairs. Flocculus whitish to golden. Femoral and tibial scopae with moderately long, simple to weakly plumose golden hairs (Fig. 233). Tergal discs with sparse, minute inconspicuous white hairs medially, and weak tufts of short white hair laterally; disc 1 additionally with few short black hairs basolaterally. Tergal marginal zones 2–4 with weak, narrow interrupted bands of sparse short white hair. Terminal fringe light brown to black, with flanking white hairs (Fig. 232). Sternal marginal zones with distinct bands of medium-lengthed whitish to golden hair (Fig. 233). Head (Figs. 230–231). 1.2–1.3 times broader than long. Mandible bidentate. Galea shagreened. Labral process rectangular, much broader than long, mostly smooth. Clypeus almost flat, shagreened and mat except for small medioapical area that is smooth and shiny, densely and distinctly punctured, distance between punctures 1–1.5 puncture diameters, with distinct narrow impunctate midline (Fig. 230). Lower part of paraocular area shagreened, densely and finely punctured; upper part and frons longitudinally striated, interspersed with fine punctures. Flagellomere 1 about as long as 2+3+4, 2 as long as 3 or slightly shorter. Facial foveae long and narrow, 0.4 times as broad as antennocular distance, extending from level of middle of lateral ocellus to slightly below antennal socket, outer margin almost reaching compound eye (Figs. 230–231). Distance of fovea from lateral ocellus 2–2.5 ocellus diameters. Ocelloccipital distance about 1.4 ocellus diameters. Vertex moderately carinate. Genal area 1.4 times broader than compound eye (Fig. 231). Mesosoma (Fig. 231). Dorsolateral angle of pronotum distinctly elevated, not forming a lateral carina. Mesonotum fully shagreened, shallowly punctured, distance between punctures about 1 puncture diameter; scutellum similar, punctation stronger (Fig. 231). Mesepisternum and propodeum alveolate-reticulate, impunctate. Propodeal triangle narrow, very finely alveolate, medioapical area more finely sculptured, basal margin occasionally with very narrow band of radial rugae (Fig. 231). Inner side of hind tibia not carinate. Inner hind tibial spur straight and of uniform width, apex curved. Hind pretarsal claw with distinct inner tooth. Nervulus interstitial to slightly postfurcal (Fig. 233). Metasoma (Fig. 232). Tergal discs shiny, sparsely and very finely punctured, distance between punctures about 4 puncture diameters; disc 1 very superficially shagreened to almost smooth, 2–4 weakly shagreened. Tergal marginal zones shiny, weakly shagreened, 2–4 weakly depressed. Pygidial plate with impunctate, slightly raised margin, without elevated medial area. Male (Fig. 234). Body length: 7–7.5 mm. Colour. Similar to female. Clypeus and paraocular areas black (Fig. 235). Pubescence. Clypeus with dense, long, white plumose hairs, especially dense on apical margin (Figs. 234, 235). Paraocular area with thin, minutely plumose black hairs, becoming longer towards ventral part. Scape and area around antennal sockets with medium to long white hairs and few black hairs (Fig. 235). Vertex with long, erect, mostly white hairs. Genal area with medium-lengthed black hairs dorsally, longer white hairs ventrally. Scutellum, metanotum and periphery of mesonotum with mixed black and white, short to long, minutely plumose hairs (Figs. 234, 236). Mesepisternum with long plumose hairs, black on dorsal part, white on ventral part. Lateral part of propodeum with long plumose hairs, mostly black, a few white. Femora and fore- and mid-tibiae with black and white hairs. Hind tibia with white hairs. Tarsi with white to golden hairs (Fig. 234). Tergal discs with sparse, minute inconspicuous white hairs medially, and sparse short white hair laterally; disc 1 additionally with few medium black hairs basolaterally. Tergal marginal zones 2–5 with very sparse short white hair laterally, not forming distinct hair bands. Terminal fringe whitish-golden (Fig. 237). Head (Figs. 235–236, 238). 1.3 times broader than long. Mandibles very long, significantly crossed (Fig. 235). Malar area with short apicoventral tooth at the base of the mandible (Fig. 238). Labral process short and broad, appressed and inconspicuous. Clypeus slightly elevated, apical part much broader than basal part, fully shagreened, distinctly punctured, distance between punctures 0.5–2 puncture diameters, punctures sparser medioapically, without impunctate midline (Fig. 235). Lower part of paraocular area shagreened, densely and finely punctured; upper part and frons longitudinally striated, interspersed with fine punctures. Flagellomere 1 longer than 2+3, 2 as long as 3 or slightly shorter. Ocelloccipital distance 2 ocellus diameters. Vertex moderately carinate. Genal area 1.7 times broader than compound eye, dorsoposterior margin weakly carinate (Fig. 236). Mesosoma (Fig. 236). Dorsolateral angle of pronotum strongly elevated and pointed, forming a strong lateral carina. Mesonotum fully shagreened, very shallowly and inconspicuously punctured, distance between punctures about 1 puncture diameter; scutellum shagreened, densely and distinctly punctured (Fig. 236). Mesepisternum and propodeum alveolate-reticulate, impunctate. Propodeal triangle very narrow, very finely sculptured, without rugae (Fig. 236). Nervulus interstitial to slightly postfurcal (Fig. 234). Metasoma (Fig. 237). Similar to female, but tergal discs shinier and very superficially shagreened. Genitalia and hidden sterna (Figs. 239–241). Dorsal gonocoxite lobes weakly developed, rounded. Gonostyli broadening apically, blade flattened and spatulate, inner apical margin distinctly concave. Penis valves broad basally, gradually narrowing apically (Fig. 239). Sternum 8 columnar, apical process slightly broadened (Fig. 240–241). Diagnosis. Andrena ornithogali is related to a group of species formerly classified under Margandrena or Ptilandrena, which possess elongate labial palpi, enlarged male gena and mandibles, and/or male genitalia with conspicuously widened penis valves (Wood 2021a; Pisanty et al. 2022). Four of these species (A. karia Wood, A. krausiella Gusenleitner, A. menahemella Scheuchl & Pisanty and A. sibthorpi Mavromoustakis) have at least partially red-marked terga, and thus cannot be confused with A. ornithogali. From the remaining five species (A. crocusella Pisanty & Scheuchl, A. elsei Scheuchl & Gusenleitner, A. grossella Grunwaldt, A. hyacinthina Mavromoustakis, A. muscaria Warncke), A. ornithogali differs in the shorter glossa, maxillary and/or labial palps (longer in A. crocusella, A. grossella and A. hyacinthina); toothed malar area (unique to this species); short, mostly shagreened and mat clypeus (shinier in A. crocusella, A. grossella and A. hyacinthina, more elongate in A. hyacinthina and A. muscaria); broader fovea (narrower in A. crocusella, A. elsei and A. hyacinthina, tapering below in A. muscaria); weakly carinate male gena, without modifications (strongly carinate in A. hyacinthina, pointed posteroventrally in A. muscaria, mostly unmodified in A. crocusella and A. grossella); almost impunctate mesonotum (more distinctly punctured in A. crocusella and A. hyacinthina); finely alveolate propodeal triangle, mostly lacking rugae (distinctly rugose basally in A. crocusella, A. elsei, A. grossella and A. hyacinthina); poorly developed dorsal gonocoxite lobe (strongly developed in A. muscaria); penis valves without pointed lateral extensions (present in A. crocusella and A. grossella); and hook-shaped apex of gonostylus, with concave inner margin (unique to this species). The presence of a malar area tooth in the male (Fig. 238) is unusual and apparently unique among the Chrysandr ena + Euandrena + Margandrena + Ptilandrena clade (Pisanty et al. 2022), and is characteristic of other subgenera, especially Hoplandrena and Andrena s.s. (in the latter, the tooth is present on the mandible itself, rather than the malar area). However, A. ornithogali is most probably unrelated to these lineages, which are also characterised by broad facial foveae, a complete propdeal corbicula (in Andrena s.s.), peripherally smooth propodeal triangle (in Hoplandrena), distal position of recurrent vein 1, and centrally elevated pygidial plate. Similar instances of convergent trait evolution in Andrena have been documented in various other male characters (Pisanty et al. 2022). Distribution: North and central Israel, Syria. Likely present also in Lebanon. Flight period: December–April. Flower records: Asparagaceae: Ornithogalum lanceolatum; Asteraceae: Taraxacum cyprium. Pollen analysis. Eight pollen loads were examined, six from Odem Forest and two from Bloudan. The pollen loads from Odem Forest contained pure Ornithogalum - type pollen, confirming field observations. However, the two samples from Bloudan contained pure pollen from an unknown monocotyledon species (Liliaceae sensu lato). This should be further investigated, but the use of a different host plant could explain the different flight periods of the sampled populations which may be adapted to local conditions and plant availability in each area. Holotype: ISRAEL: Odem Forest Nature Reserve [Ya’ar Odem NR], 27.ii.2020, G. Pisanty, pan trap, ♀ (SMNHTAU:331858). Paratypes: ISRAEL: Horbat Nappah [Golan, Nafech], 1.i.1974, A. Freidberg (1♀); Jerusalem,?.ii.? (1♀); Mount Hermon [Har Hermon], 1645 m, 33.2994°N 35.7675°E, 16.iv.2021, G. Pisanty (1♀); Odem Forest Nature Reserve [Ya’ar Odem N.R.], 1.iii.2018, G. Pisanty (58♀); [Ya’ar Odem NR], 27.ii.2020, G. Pisanty, pan traps (241♀); 33.186°N 35.7356°E, 27.ii.2020, G. Pisanty, sweeping (6♀); 33.206°N 35.736°E, 27.ii.2020, G. Pisanty, on Ornithogalum lanceolatum (8♀); 33.207°N 35.736°E, 2.i.2021, on Ornithogalum lanceolatum (2♂); [Ya’ar Odem NR, Jubat Al Kabira], 33.206°N 35.736°E, 21.xii.2020, G. Pisanty, pan trap (1♂); 2.i.2021, pan traps (2♀, 22♂); 33.207°N 35.732°E, 21.xii.2020, G. Pisanty (1♂); 33.207°N 35.736°E, 2.i.2021, on Taraxacum cyprium (8♂); SYRIA: Bloudan [Bludan], 57 km NW Damaskus, 24.iv.1992, K. Warncke (3♀, 2♂) (ES, NHMUK, OLML, RMNH, SMNHTAU, TJW, ZMHB, ZSMC). Etymology. Named after the plant genus Ornithogalum, which seems to be the main pollen host for the Golan Heights population. The species epithet is an adjective. Not to be confused with Andrena ornithogala nomen nudum, an unpublished name applied by Warncke to a Micrandrena taxon from Turkey.
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- 2022
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41. Andrena (Aciandrena) obtusa Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
- Author
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Insecta ,Arthropoda ,Andrena obtusa ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Aciandrena) obtusa Pisanty sp. nov. (Figs. 27–35) Female (Fig. 27). Body length: 6–6.5 mm. Colour. Head and mesosoma dark brown to black (Fig. 27). Anterior side of flagellomeres 4–10 orange (Fig. 27–28). Legs brown to black, apical tarsomeres light brown. Wings slightly infuscate, veins brown, stigma golden, often partly translucent medially (Fig. 27). Tergal discs brown. Tergal marginal zones reddish-orange basally, white apically (Fig. 30). Pubescence. Body hair mostly sparse, short, minutely plumose, white to yellowish-white (Fig. 27). Head and mesosoma mostly with white hair ventrally and yellowish hair dorsally (Fig. 27). Clypeus with sparse short white hair. Paraocular area and area around antennal sockets with dense short white hair (Fig. 28). Facial foveae dark in ventral view, white to brownish-white in dorsal view (Fig. 29). Vertex with white to golden, medium-lengthed hair. Genal area with short yellowish hair dorsally, medium white hair ventrally. Mesonotum and scutellum with short brownish-white hairs, relatively sparse and thin medially, dense and thick peripherally (Fig. 29). Mesepisternum with long white hair. Propodeal corbicula incomplete, dorsoposterior fringe with long white plumose hair, corbicular surface with few long, white simple hairs. Femora and tibiae with mostly short white hair, tarsi with short white to golden hair; scopal hairs simple, white; flocculus incomplete, white (Fig. 27). Tergal discs with short white hair laterally; medially, 1–2 with extremely sparse and minute inconspicuous hair; 3–4 with sparse short white hair; 5 with relatively long white hair, merging into prepygidial fimbria. Tergal marginal zones 2–4 with dense bands of white hair covering bases of following tergal discs, interrupted in 2–3, continuous in 4. Prepygidial fimbria white, pygidial fimbria golden (Fig. 30). Head (Figs. 28–29). 1.2 times broader than long. Mandible weakly to strongly bidentate. Galea shiny, very finely shagreened except on inner basal area. Labral process trapezoidal, apex distinctly narrower than base, basal part transversely striated. Clypeus almost completely flat, shiny, weakly shagreened basolaterally, more or less smooth medioapically, sparsely, irregularly punctured, distance between punctures 1.5–3 puncture diameters (Fig. 28). Flagellomere 1 longer than 2+3, 2 as long as 3. Frons longitudinally striated. Facial foveae of moderate width, tapering downwards, extending from level of middle–upper end of lateral ocellus to middle–lower end of antennal socket, about 0.6 times as broad as antennocular distance (Fig. 28). Distance of fovea from lateral ocellus about 0.7 ocellus diameter. Ocelloccipital distance 1 ocellus diameter. Vertex weakly carinate, almost rounded (Fig. 29). Mesosoma (Fig. 29). Pronotum without elevated dorsolateral angle or lateral carina. Mesonotum and scutellum strongly shagreened, weakly shiny, very superficially and imperceptibly punctured, distance between punctures 1–2 puncture diameters (Fig. 29). Mesepisternum finely alveolate, obliquely punctured. Propodeal corbicula finely reticulate. Posterior part of propodeum finely alveolate, triangle very weakly demarcated by weak carina, sculpturing slightly coarser basally compared to flanking areas (Fig. 29). Hind pretarsal claw unidentate. Recurrent vein 1 meets submarginal cell 2 near its middle. Submarginal crossvein 1 meets marginal cell 3–5 vein widths from stigma. Nervulus strongly antefurcal. Metasoma (Fig. 30). Tergal discs finely shagreened and impunctate, 1 strongly so, the following gradually more weakly shagreened and shinier. Tergal marginal zones similarly sculptured, weakly depressed, 2–4 distinctly arched, medially occupying 1/3–1/2 of tergum length. Pygidial plate without elevated medial zone. Male (Fig. 31). Body length: 6–7 mm. Colour. Head and mesosoma dark brown to black (Fig. 31). Clypeus white except for two small mediolateral dark maculations. Paraocular area white almost up to level of clypeal base (Fig. 32). Anterior side of flagellomeres 3–11 orange. Legs dark brown to black, apical tarsomeres light brown. Wings slightly infuscate, veins brown, stigma brownish-golden (Fig. 31). Tergal discs dark brown to black. Tergal marginal zones reddish-orange basally, yellowish-white apically (Fig. 33). Pubescence. Body hair mostly thin, white, short to medium-lengthed, minutely plumose (Fig. 31). Clypeus with dense fringe of white hairs, extending below to about half clypeus length. Paraocular area and area around antennal sockets with dense short white hair (Fig. 32). Vertex with medium-lengthed white hairs medially, short white to greyish hairs laterally (Fig. 31). Genal area with white hairs, short dorsally, medium ventrally. Mesonotum, scutellum and metanotum with relatively long, moderately dense, white to greyish thin hairs. Mesepisternum with long white hair. Lateral part of propodeum with fringe of long white plumose hairs. Femora and tibiae with white hair, tarsi with short white to golden hair (Fig. 31). Tergal discs with thin white hair of moderate density, very short on medial part of terga 2–5, longer laterally and on tergum 1. Tergal marginal zones 2–4 with interrupted bands of dense, short white hair; 5 with continuous band of medium-lengthed, sparse white hair (Fig. 33). Head (Fig. 32). 1.2 times broader than long. Labral process weakly trapezoidal, almost rectangular, apical margin emarginate. Clypeus weakly convex, almost smooth, finely punctured, distance between punctures 1–2 puncture diameters, puncture density increasing laterally, without impunctate midline (Fig. 32). Supraclypeal plate not striated. Frons longitudinally striated. Flagellomere 1 slightly shorter than 2+3, 2 shorter than 3 (Fig. 32). Ocelloccipital distance 1.2 ocellus diameters. Vertex carinate. Posterior margin of genal area more or less rounded, not carinate. Mesosoma. Similar to female, except for bidentate hind pretarsal claw. Metasoma (Fig. 33). Similar to female, but a very fine tergal punctation is weakly perceptible, distance between punctures 2–3 puncture diameters. Tergal marginal zones more weakly arched than in female, usually occupying no more than 2/5 of tergal length. Genitalia and hidden sterna (Figs. 34–35). Dorsal gonocoxite lobe weakly developed, rounded. Gonostyli elongate, finger-shaped, rounded apically. Basal half of penis valves moderately broad and strongly tapering, apical half very narrow (Fig. 34). Sternum 8 simple, columnar, of uniform width, apical process suddenly but slightly broadened (Fig. 35). Diagnosis. Andrena obtusa closely resembles A. (Aciandrena) varicornis Pérez, but differs in the broader facial foveae, slightly more flattened and shagreened female clypeus, ivory-coloured male clypeus (yellow in A. varicornis), and finger-shaped, apically rounded gonostyli (hook-shaped, apically pointed in A. varicornis). Distribution: Southern Israel. Flight period: February–April. Flower records: Asteraceae: Senecio glaucus; Brassicaceae: Erucaria microcarpa. Holotype: ISRAEL: Shivta Junction, 30. 941°N 34.597°E, 16.iii.2020, G. Pisanty, ♂ (SMNHTAU: 333575). Paratypes: ISRAEL: Holot Mash’abbim Nature Reserve [Holot Mash’abbim], 30.999°N 34.7578°E, 18.ii.2022, G. Pisanty, pan traps (2♂) and sweeping (5♂); Mashabei Sadeh [Mashabe Sade], 16.ii.1976, A. Freidberg (1♀); [N. Negev Des’t, Mash’abbe Sade, 15 km S Be’er Sheva], 16.iii.1989, C. O’Toole, on Senecio glaucus (1♂); Nahal Zin, 15.iv.2007, I. Lalzar (1♀); Retamim, 273 m, 31°03’N 34°41.5’E, 3.iv.2009, A. Freidberg (2♀, 2♂); Shivta, 17.iii.1977, A. Freidberg (1♀); Shivta Junction, 30.941°N 34.597°E, 6.iii.2020, G. Pisanty, partly from pan traps (2♀, 1♂); Tel Yeroham [Tel-Jerucham], 25.iii.1959, J. Kugler, on Erucaria microcarpa (1♂) (OLML, RMNH, SMNHTAU, TJW). Etymology. obtusus = Latin for “blunt, dull, obtuse”, in reference to the gonostyli which lack points, unlike the related species A. varicornis. The species epithet is an adjective.
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42. Andrena (Micrandrena) lunaris Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
- Author
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Andrena lunaris ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Micrandrena) lunaris Pisanty & Wood sp. nov. (Figs. 115–126) Female (Fig. 115). Body length: 6 mm. Colour. Body black (Fig. 115). Anterior side of flagellomeres 2–10 dark brown to black. Legs brown to black. Wings weakly infuscate, veins and stigma light to dark brown (Fig. 115). Tergal marginal zones dark brown to black (Fig. 120). Pubescence. Body hair mostly short, white to golden, distinctly plumose (Fig. 115). Clypeus with moderately dense, short and thin yellowish hairs (Figs. 116–117). Paraocular and supraclypeal areas, frons and scape with moderately dense, short to medium, whitish to golden hairs (Fig. 116). Upper half of fovea golden-brown in dorsal view (Fig. 118). Vertex with short to medium golden hairs. Genal area with short golden hairs dorsally, gradually white medium hairs ventrally. Mesonotum and anterior half of scutellum with dense, short and thick golden hairs (Figs. 118–119). Metanotum and posterolateral margin of scutellum with dense, medium-lengthed, thick whitish to golden hairs. Mesepisternum with long whitish to golden hairs. Propodeal corbicula incomplete, dorsoposterior fringe with long whitish plumose hairs, corbicular surface with few long simple white hairs. Legs with white to golden hairs; scopal hairs simple, whitish; flocculus incomplete, white (Fig. 115). Tergal discs 1–4 laterally with sparse short white hair; medially, 1 almost hairless, 2 and especially 3–4 with minute inconspicuous white hairs. Apices of tergal discs 2–4 with sparse fringes of medium-lengthed white hairs reaching end of marginal zone, interrupted on 2–3, continuous on 4. Tergal marginal zones 2–4 with broadly interrupted, narrow apical bands of dense short white hair, slightly extending onto following tergal disc, thinner and narrower on tergum 4. Prepygidial fimbria whitish laterally, light brown medially; pygidial fimbria light brown (Fig. 120). Head (Figs. 116–118). 1.2 times broader than long. Mandible bidentate. Galea finely shagreened. Labral process complex, basal half triangular, apical half snout-shaped, weakly protuberant (Fig. 117). Clypeus weakly convex, shagreened, apical margin often smooth, punctation fine, distance between punctures 1–2 puncture diameters, with a broad impunctate midline (Figs. 116–117). Supraclypeal plate, paraocular area and frons strongly longitudinally striated, a strong punctation is developed mainly on lower half of paraocular area and above antennal sockets (Fig. 116). Flagellomere 1 about as long as 2+3. Facial foveae elongate, of moderate, uniform width, extending from level of middle–lower end of lateral ocellus to base of clypeus or slightly above, 0.3 times as broad as antennocular distance (Figs. 116, 118). Distance of fovea from lateral ocellus 1.5 ocellus diameters. Ocelloccipital distance slightly less than 1 ocellus diameter. Vertex moderately carinate (Fig. 118). Mesosoma (Fig. 118). Pronotum without elevated dorsolateral angle or lateral carina. Mesonotum finely and very densely punctured, distance between punctures 0–0.5 puncture diameters, anterior part with punctures becoming oblique and blending into shagreenation (Fig. 119). Scutellum similarly punctured, often somewhat shinier (Fig. 118). Mesepisternum finely alveolate, obliquely punctured. Propodeal corbicula finely reticulate, with few very coarse, oblique punctures. Posterior part of propodeum strongly right-angled, posterolateral part rugose-areolate; triangle weakly delineated by shallow carina, basal 1/3–1/2 rugose-areolate, apical 1/2–2/3 finely alveolate, a strong mediobasal carina is sometimes developed (Fig. 118). Hind pretarsal claw bidentate. Recurrent vein 1 meets submarginal cell 2 at its middle or slightly proximal to it. Submarginal crossvein 1 meets marginal cell 1–2 vein widths from stigma. Nervulus slightly antefurcal to interstitial (Fig. 115). Metasoma (Fig. 120). Tergal discs shagreened, shagreenation decreasing towards apical terga; 1 impunctate, 2–4 finely, very densely and very shallowly punctured, punctation blending into shagreenation and hardly discernible. Tergal marginal zones broad, arched, medially covering 1/2–3/5 of tergal length, impunctate, shagreened to shallowly reticulate, shagreenation decreasing towards apical terga. Male (Fig. 121). Body length: 5.5 mm. Colour. Similar to female. Pubescence. Facial hair colour variable among individuals, ranging from fully white to predominantly black in some areas of the face, especially the paraocular area and frons(Figs. 121–122).Clypeus with dense fringe of mediumlengthed white hairs, extending beyond clypeal apex to about 1/2 of clypeus length (Figs. 121–122). Paraocular area with moderately dense, short to medium, white to black hairs. Scape and area between antennal sockets with dense, medium-lengthed white to mixed black and white hairs. Frons with sparse, short to medium, white to black hairs. Vertex with short white to black hairs and long white to golden hairs. Genal area with short white to black hairs dorsally, gradually medium-lengthed, white ventrally. Mesonotum, scutellum and metanotum with moderately dense, short to medium, white to golden hairs, longer and denser peripherally (Figs. 121, 123). Mesepisternum with long white hairs, sometimes golden dorsally (Fig. 121). Propodeum with long whitish hairs. Legs with white to golden hair. Tergal discs 1–5 laterally and 1 basally with short white to yellowish hair; 1–5 medially with minute inconspicuous bright hair. Apices of tergal discs 2–4 with sparse fringes of medium-lengthed, white to golden thin hairs reaching end of marginal zone, interrupted on 2–3, continuous on 4. Tergal marginal zones 2–4 with broadly interrupted, narrow apical bands of moderately dense short white hair, slightly extending onto following tergal disc (Fig. 124). Head (Fig. 122). 1.2 times broader than long. Labral process square, apical margin strongly emarginate. Clypeus weakly convex, shagreened to shiny, transversely striated, moderately punctured, distance between punctures 0.5–1 puncture diameters, a narrow impunctate midline is sometimes weakly indicated. Supraclypeal and paraocular areas and frons distinctly rugose. Flagellomere 1 shorter than 2+3, 2 shorter than 3. Ocelloccipital distance 1 ocellus diameter. Vertex carinate. Mesosoma (Fig. 123). Similar to female, but mesonotal punctation sparser and very shallow, blending into shagreenation, distance between punctures 0.5–1 puncture diameters (Fig. 123). Metasoma (Fig. 124). Similar to female, tergal marginal zones 2–4 narrower, medially occupying 1/3–1/2 of tergal length. Genitalia and hidden sterna (Figs. 125–126). Dorsal gonocoxite lobes weakly developed, apices pointed, adjacent to one another. Gonostyli broadening apically, blade flat, rounded. Basal half of penis valves relatively broad, spade-shaped, apical half needlelike (Fig. 125). Sternum 8 simple, columnar, densely and uniformly hairy, weakly broadening apically, apical margin blunt to weakly emarginate (Fig. 126). Diagnosis. Andrena lunaris is distinguished from other Micrandrena by the combination of the elongate, slightly protuberant, snout-shaped labral process (Fig. 117), and the extremely densely punctate and dull mesonotum covered by relatively dense and thick short hair (Figs. 118–119). The male is easily identified by the unique shape of the genitalia (Fig. 125). Distribution: North and central Israel, Jordan, Syria, West Bank. Flight period: February–April. Flower records: Amaryllidaceae: Allium trifoliatum; Asparagaceae: Ornithogalum narbonense; Asteraceae: Glebionis sp.; Brassicaceae: Diplotaxis erucoides, Sinapis alba; Orchidaceae: Cephalanthera longifolia. Holotype: ISRAEL: Montfort, Nahal Kziv [Montfort, Nahal Keziv], 28.ii.2018, G. Pisanty, ♀ (SMNHTAU:286280). Paratypes: ISRAEL: Adulam-France Park [Ya’ar Adulam], 20.ii.2013, Y. Berner, on Diplotaxis erucoides (4♂); [Ya’ar Adullam], 20.iv.2011, T. Koznichki, pan trap (1♀); Bar’am, 4.iv.2014, N. Atkin, on Sinapis (1♀) & O. Winberger, on Glebionis and from pan traps (2♀); Beit Keshet [Bet Qeshet], 1.5 km NW, 32.74°N 35.38°E, 20.ii.2019, G. Pisanty (3♂); Beit Oren [Bet-Oren], 16.ii.1990, R. Kasher (1♂); Bnei Dror [Bené Deror], 7.iii.2012, O. Afik, partly from pan traps (4♀, 2♂); Buraiqa Nature Reserve [Buraiqa NatReserve], 32.5413°N 34.979°E, 15.ii.2021, G. Pisanty (1♂); Dishon, 7.iv.2016, O. Winberger, pan traps (1♀); Forest of the Martyrs [Ya’ar Kedoshim], 2.iii.2014, N. Shamir, pan traps (1♂); 4.iii.2014, N. Shamir, pan traps (1♂); 6.iii.2014, N. Shamir, pan traps (1♀); 7.iii.2014, N. Shamir, pan traps (1♂); 23.iii.2014, N. Shamir, on Allium trifoliatum (3♀) and Sinapis alba (1♀); 24.iii.2014, N. Shamir, pan traps (1♂); 26.iii.2014, N. Shamir, pan traps (2♀); 30.iii.2014, N. Shamir, pan traps (1♀); 7.iii.2017, Y. Farago, pan traps (1♀); 18.iii.2017, Y. Farago, pan traps (5♀, 1♂); 3.iv.2017, Y. Farago, pan traps (1♀); 16.iv.2017, Y. Farago, pan traps (2♀); Give’at Humera [Humra Hill], 12.iii.2009, A. Dorchin (1♀); Goren, 33°02’47.7’’N 35°13’19.8’’E, 25.iii.2021, T. Novoselsky (1♀); Haifa, 26.ii.1977, A. Freidberg (1♀); 20.iii.1979, A. Dafni, on Cephalanthera longifolia (1♂); Hanita, 27.iii.1976, D. Gerling (1♀); Har Karmila, 340 m, 31°47.7’N 35°00.9’E, 27.iii.2011, A. Freidberg (1♂); Har Tayyasim, 740 m, 31°46.3’N 35°05.1’E, 27.iii.2011, A. Freidberg (1♀); Harutzim [Harutsim], 26.ii.2009, A. Dorchin (1♀, 1♂); Hirbet Samara, 2.iii.2009, A. Dorchin (5♀, 1♂); Horbat Sheqofa, 252 m, 31.5775°N 34.8709°E, 15.iii.2021, G. Pisanty, pan trap (1♀); Kadima [Qadima], 5.iii.1990, R. Kasher (1♀); Kiryat Tiv’on [Tiv’on], 6.ii.1975, H. Bytinski-Salz (1♂); Lakhish, 23.ii.2012, T. Shapira, pan traps (11♂); 18.ii.2013, T. Shapira, pan traps (3♂); 6.iii.2013, T. Shapira, pan traps (2♀); 15.iii.2013, T. Shapira, pan traps (1♂); 18.iii.2013, T. Shapira, pan traps (1♀); 19.iii.2013, T. Shapira, pan traps (8♀); 2 km E, 31.556°N 34.87°E, G. Pisanty, 5.ii.2016, G. Pisanty, pan trap (1♂); 31.5562°N 34.869°E, 4.iii.2016, pan trap (1♀); 31.557°N 34.870°E, 4.iii.2016, pan traps (2♀); 3 km NE, 31.575°N 34.870°E, 11.iii.2016, G. Pisanty, pan trap (1♀); 31.578°N 34.870°E, 19.ii.2016, G. Pisanty (1♂); 26.ii.2016, G. Pisanty, partly from pan traps (1♀, 5♂); 31.579°N 34.871°E, 4.iii.2016, G. Pisanty, pan trap (1♀); Lehavot HaBashan [Lahavot HaBashan], 1.iii.2018, G. Pisanty (1♀); Malkia [Malkiyya], 10.iv.2014, O. Winberger, pan traps (3♀); 19.iv.2016, O. Winberger, pan traps (13♀); Me’arat Yishah, 0.5 km E, 32.718°N 35.007°E, 22.ii.2019, G. Pisanty (2♂); Mi’ilya–Montfort Road [Meiliya Mt.Fort Rd.], 5.iv.1972, D. Gerling (1♂); Montfort, 17.iii.1983, A. Freidberg (1♂); 33.045°N 35.225°E, 26.ii.2021, G. Pisanty (1♀, 1♂); [Monfort], 4.iii.1976, A. Freidberg (1♀, 2♂); 10.iii.1981, F. Kaplan (3♂) & T. Furman (1♂); [Montfort, Nahal Keziv], 28.ii.2018, G. Pisanty (2♀, 10♂); Mount Carmel, Hay-Bar, 1 km S University, 25.iii.1990, R. Kasher (2♀); Mount Meron, 900 m, 13.iv.1988, I. Yarom (1♂); [Har Meron], 32.9945°N 35.415°E, 5.iv.2016, G. Pisanty (1♀); 33.000°N 35.3927°E, 4.iv.2017, G. Pisanty, pan traps (1♀, 2♂); 1000 m, 1.iv.2012, A. Freidberg (1♂); 1100 m, 17.iv.2000, A. Freidberg (1♀); [W.Habiz, Mt. Meron], 8.iv.1972, A. Kesar (1♂); Mount Meron Nature Reserve [Meron NR], 1.2 km SSW Meron Field School, 998 m, 32°59’55’’N 35°23’31’’E, 3.iv.2016, A. Dorchin (1♀); Nahal Alexander, 4.iii.2017, K. Levy, pan trap (1♀); Nahal Dishon, 1.iv.1991, R. Kasher (2♂); Nahal Kziv [Nahal Keziv], 33.0465°N 35.226°E, 26.ii.2021, G. Pisanty (6♀, 23♂); 33°02.7’N 35°13.6’E, 5.iii.2008, A. Freidberg (1♂); [W. Habiz, Upper Galilee], 3.iv.1972, D. Gerling (2♀, 1♂); Ness Ziona [Nes Ziyyona], 31.928°N 34.78°E, 13.iii.2015, G. Pisanty (1♀); Netanya, Irus Ha’Argaman Nature Reserve [Irus Ha’Argaman NR], 32.287°N 34.842°E, 24.ii.2021, G. Pisanty (2♂); Netiv HaLamed-Heh [Netiv Halamed He], 24.ii.2009, G. Pisanty, pan traps (4♂); 26.ii.2009, G. Pisanty, pan trap (1♂); Ramat HaNadiv, 22.iii.2012, T. Shapira, pan trap (1♀); 11.iv.2012, T. Shapira, pan traps (2♀); 12.iv.2012, T. Shapira, pan traps (2♀); 2.iv.2013, T. Shapira, pan trap (1♀); [Hasharon, Zikhron Ya’aqov, Ramas Hanadiv], 12.iii.1990, R. Leys (2♀); [R. Hanadiv], 4.iii.1990, R. Kasher (1♂); Sasa, 1.iv.2014, O. Winberger, pan trap (1♂); 29.iv.2014, O. Winberger, pan trap (1♀); 3.iv.2016, O. Winberger, pan trap (1♂); Sheikh Ali, 20 km E Qiryat Gat, 17.iii.1990, R. Kasher (2♀); Shoham, 17.iii.2010, L. Friedman (1♀); 22.iii.2012, L. Friedman (2♀); Snir, Hermon Field Study Center, 13.iii.1997, R. Kasher (2♀); 27.iii.1997, R. Kasher (2♀, 1♂); 30.iii.1997, R. Kasher (1♀); Ya’ar Nehusha [Ya’ar Nehosha], 22.iii.2016, T. Chaprazaro, on Ornithogalum narbonense (1♀); Yiftah [Yiftach], 30.iii.2016, O. Winberger, pan traps (1♀); Zur Natan, 500 m NE, 32.245°N 35.021°E, 6.iv.2020, G. Pisanty (1♀); JORDAN: 10 km N Jerash, 20.iv.2002, M. Snižek (1♀); SYRIA: Burg Marqab, 7 km SE Banyas, 16.iv.1992, K. Warncke (36♀, 1♂); WEST BANK: Har Kabbir, 700 m, 17.iii.2015, L. Friedman (1♂); Kedumim [Qedumim], 20.ii.2006, L. Friedman (1♂); Maskiot [Maskiyyot], Rt. 578, Wadi Halat Mahmud el-‘ Ali, – 75 m, 32°19’18’’N 35°29’52’’E, 27.ii.2020, L. Friedman (1♀); Nahal Teqoa, 31°38’N 35°14’E, 31.iii.2009, A. Freidberg (1♀) (ES, NHMUK, OLML, RMNH, SMNHTAU, TJW, ZMHB, ZSMC). Etymology. lunaris = Latin for “lunar”, in reference to the sculptuting of the mesonotum which appears to be marked with crater-like punctures, like the surface of the moon. The species epithet is an adjective.
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- 2022
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43. Andrena (Micrandrena) sillata Warncke 1975
- Author
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Andrena sillata ,Hymenoptera ,Taxonomy - Abstract
Andrena (Micrandrena) sillata Warncke, 1975 Distribution: Greece, Turkey (Gusenleitner & Schwarz 2002). Newly recorded from Israel, Jordan, Lebanon, Syria and the West Bank. Warncke (1974c) mentions the species is limited to high elevations (above 1300 m); in Israel, however, it can be found even below 1000 m. Krainov (2013) mentions this species from western Siberia in Russia, which is unlikely. Flight period: February-May (Israel), April–June (Turkey, Warncke 1974c). Flower records: Rosaceae: Prunus dulcis, Pyrus syriaca; Sapindaceae: Acer monspessulanum. Material examined: HOLOTYPE: TURKEY: Akseki / Taurus, 1300 m, 25.iv.1973, K. Warncke (♀) (OLML); PARATYPES: GREECE: Rhodes, Profitis Ilias, 20.iv.1970, H. Teunissen (1♀); TURKEY: Akseki / Taurus, 1300 m, 25.iv.1973, K. Warncke (1♂) (OLML); non-type material: ISRAEL: Bar’am, 4.iv.2014, O. Winberger, pan traps (2♀); 1.iv.2016, O. Winberger (2♀); Dovev, 14.iv.2016, O. Winberger (1♀); Har Addir, 33.033°N 35.361°E, 5.iv.2016, G. Pisanty, pan trap (1♀); Har Avital, 15.iii.1995, R. Kasher (1♀); Hermon Nature Reserve [Hermon NR], Har Kahal, 1368 m, 33.286°N 35.736°E, 28.v.2019, L. Friedman (1♀); [Hermon NR], Har Shezif, 1447 m, 33.286°N 35.7524°E, 16.iv.2022, G. Pisanty, pan traps (3♂); Jish [Gush Halav], 31.iii.2016, O. Winberger (1♂); Kfar Giladi [Kefar Giladi S], 12.iv.1997, R. Kasher (1♀); 14.iv.1997, R. Kasher (1♀); Kfar Shamai [Kfar Shammay], 13.iv.1988, I. Yarom (1♀); Meron Junction [Meron JNC.], 20.iii.1995, on Pyrus syriaca (5♀); Montfort [Nahal Keziv, Montfort], 33°02.6’N 35°13.3’E, 4.iii.2010, L. Friedman (2♂); Mount Hermon [Har Hermon], 1420 m, 33.2855°N 35.763°E, 7.iv.2021, G. Pisanty, pan traps (5♂); 1540 m, 33.296°N 35.763°E, 7.iv.2021, G. Pisanty, pan traps (3♂); 1610 m, 33.300°N 35.767°E, 7.iv.2021, G. Pisanty, pan traps (3♂); 1640 m, 33.300°N 35.7675°E, 7.iv.2021, G. Pisanty, sweeping (3♂); 1642 m, 33.2996°N 35.7677°E, 16.iv.2022, G. Pisanty, pan traps (5♂); 1644 m, 33.2991°N 35.7667°E, 16.iv.2022, G. Pisanty, pan traps (43♂); 33.2992°N 35.7670°E, 16.iv.2022, G. Pisanty, pan traps (30♂); 1645 m, 33.2994°N 35.7675°E, 16.iv.2021, G. Pisanty, pan traps (98♂) and sweeping (4♂); 1649 m, 33.2993°N 35.7679°E, 16.iv.2021, G. Pisanty, on Acer monspessulanum (2♂); [Hermon], 1641 m, 33.2993°N 35.7670°E, 16.iv.2022, G. Pisanty, on Prunus dulcis (1♂); 1642 m, 33.2992°N 35.7668°E, 16.iv.2022, G. Pisanty, on Rosaceae (1♂); Mount Meron [Har Meron], 32.9987°N 35.392°E, 21.iv.2016, G. Pisanty, pan traps (2♀); 33.00°N 35.395°E, 15.v.2015, G. Pisanty (2♀); 33.000°N 35.3925°E, 21.iv.2016, G. Pisanty, (9♀); 33.000°N 35.3927°E, 4.iv.2017, G. Pisanty, pan traps (5♀, 13♂); 1000 m, 1.iv.2021, L. Friedman (1♀); 17.iv.2012, L. Friedman (1♀); 1000 m, 32º59.7’N 35º24.7’E, 14.iv.2011, L. Friedman (2♀); 1100 m, 17.iv.2000, A. Freidberg (1♀, 1♂); [Har Meron], 4 km E, 9.iv.1988, R. Leys (1♂); [Meiron], 23.iv.1973, M. Kaplan (1♀); [Meron], 23.iv.1973, D. Furth (1♀); [MtMeron], 1000 m, 13.iv.1988, I. Yarom (1♀); [W. Habiz, Mt. Meron], 8.iv.1972, H. Lebel (1♂); Mount Meron Nature Reserve [Meron NR], 1.2 km SSW Meron Field School, 998 m, 32º59’55’’N 35º23’31’’E, 3.iv.2016, A. Dorchin (1♀); Odem Forest Nature Reserve [Ya’ar Odem N.R.], 1.iii.2018, G. Pisanty (1♀, 2♂); [Ya’ar Odem NR], 33.205°N 35.736°E, 27.iv.2020, G. Pisanty, pan traps (3♀); 33.206°N 35.736°E, 27.ii.2020, G. Pisanty, pan trap (1♂); Sasa, 1.iv.2014, O. Winberger, pan traps (2♀); 20.iv.2015, O. Winberger, pan trap (1♀); 27.iv.2015, O. Winberger, pan trap (1♀); 3.iv.2016, O. Winberger (2♀, 2♂); 14.iv.2016, O. Winberger (2♀, 2♂); Snir, Hermon Field Study Center, 21.iii.1997, R. Kasher (1♀); Ziv’on, 1 km SW, 33.019°N 35.407°E, 5.iv.2016, G. Pisanty (1♀); 33.02°N 35.41°E, 21.iv.2016, G. Pisanty (1♀); JORDAN: 10 km N Jerash, 20.iv.2002, M. Snižek (1♀); LEBANON: Ras El Beida, 3.iv.1978, D. Gerling (1♀); SYRIA: Bloudan [Bludan], 57 km NW Damascus, 2000 m, 24.iv.1992, K. Warncke (1♀, 8♂); Slanfah [Slenfe], 19.iv.1986, K.M. Guichard (1♀); WEST BANK: Azzun [Azun], 7.iii.1973, M. Kaplan (1♀) (NHMUK, OLML, RMNH, SMNHTAU, TJW)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 59, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Warncke, K. (1975) Die Sandbienen der Turkei (Hymenoptera, Apoidea, Andrena), Teil B. Beschreibungen der neuen Andrena - Arten bzw. Unterarten. Mitteilungen der Munchner Entomologischen Gesellschaft, 65, 29 - 102.","Gusenleitner, F. & Schwarz, M. (2002) Weltweite Checkliste der Bienengattung Andrena mit Bemerkungen und Erganzungen zu palaarktischen Arten (Hymenoptera, Apidae, Andreninae, Andrena). Entomofauna, Supplement 10, 1 - 1280.","Warncke, K. (1974 c) Die Sandbienen der Turkei (Hymenoptera, Apoidea, Andrena), Teil A. Mitteilungen der Munchner Entomologischen Gesellschaft, 64, 81 - 116.","Krainov, I. V. (2013) Zoogeographical characteristics of the Andrenidae (Hymenoptera, Apiodea, Andrenidae) in the Western Siberia. ФuнdaмiнtaЛЬныi IССЛidOVaнIЯ, 8, 892 - 895. [in Russian]"]}
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- 2022
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44. Andrena (Aciandrena) curviocciput Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
- Author
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
- Subjects
Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Andrena curviocciput ,Hymenoptera ,Taxonomy - Abstract
Andrena (Aciandrena) curviocciput Pisanty & Wood sp. nov. (Figs. 10–17) Female (Fig. 10). Body length: 5.5 mm. Colour. Body dark brown to black (Fig. 10). Anterior side of flagellum gradually becoming orange apically (Figs. 10–11). Distal tarsal segments reddish-brown. Wings slightly infuscate, stigma brown peripherally, yellowish to brown medially, veins light to dark brown (Fig. 10). Tergal marginal zones yellowish to dark brown (Fig. 13). Pubescence. Body hair mostly short, minutely plumose, white to golden (Fig. 10). Clypeus and mandibles with short golden hairs. Supraclypeal and paraocular areas, frons and vertex with short whitish hairs (Fig. 11). Facial foveae with minute whitish to brownish hairs. Genal area with short hair, whitish dorsally, golden ventrally. Mesonotum with sparse, minute inconspicuous hairs. Scutellum and metanotum with short whitish hairs (Fig. 12). Mesepisternum with long white hairs. Propodeal corbicula incomplete, dorsoposterior fringe with sparse, long white plumose hairs. Surface of corbicula with sparse, long white simple hairs. Leg hair white to golden (Fig. 10). Scopal hairs simple, whitish. Flocculus incomplete, white. Tergal discs with sparse, minute, inconspicuous white hair. Tergal marginal zones 2–4 with narrow lateral bands of short hair, white on 2–3, white to golden on 4. Prepygidial fimbria golden medially, white laterally; pygidial fimbria golden (Fig. 13). Head (Fig. 11). 1.2–1.3 times broader than long. Labral process trapezoidal, apex much narrower than base. Clypeus weakly convex, shiny, superficially shagreened, punctures of moderate size and strength, puncture density 1–2 puncture diameters, a broad impunctate midline is sometimes partly to fully developed (Fig. 11). Paraocular area shiny, finely longitudinally striated, densely and more finely punctured, distance between punctures 0–0.5 puncture diameters. Flagellomere 1 about as long as 2+3, 2 as long as 3. Frons shiny, superficially shagreened, finely and weakly punctured, distance between punctures about 2 puncture diameters. Facial fovea 0.6 times as broad as antennocular distance, extending from almost upper end of lateral ocellus to lower end of antennal socket or slightly below. Upper 3/5 of fovea shallow, gradually tapering, lower 2/5 deeper, almost linear, separated from compound eye by smooth area (Fig. 11). Distance of fovea from lateral ocellus about 0.8 ocellus diameters. Vertex strongly arched, lateral ocelli reaching preoccipital ridge (ocelloccipital distance zero) (Figs. 11–12). Genal area as broad as compound eye (Fig. 10). Mesosoma (Fig. 12). Mesonotum and scutellum shiny, superficially shagreened and weakly punctured, distance between punctures 2–4 puncture diameters on mesonotum and 1–2 on scutellum (Fig. 12). Mesepisternum, propodeal corbicula and posterolateral part of propodeum shiny, finely reticulate, impunctate. Propodeal triangle equilateral, more coarsely reticulated than rest of propodeum, with narrow basal band of longitudinal rugae (Fig. 12). Tarsal claws unidentate. Recurrent vein 1 reaching submarginal cell 2 at its middle or slightly closer to submarginal crossvein 1. Nervulus distinctly antefurcal. Metasoma (Fig. 13). Tergal discs shiny, impunctate, finely shagreened except on apical parts of 2–4. Tergal marginal zones weakly depressed, shiny, superficially shagreened, impunctate, occupying 0.3–0.4 of tergal width. Pygidial plate V-shaped, flat. Male (Fig. 14). Body length: 5.5 mm. Colour. Similar to female. Clypeus and paraocular areas dark (Fig. 15). Pubescence. Genal area with long hair ventrally, mostly white (Fig. 14). Rest of body hair similar to female, but generally brighter, usually white (Fig. 14). Head (Figs. 15–16). Labral process broad, rectangular-trapezoidal, apex not much narrower than base. Ocelloccipital distance about 0.3 ocellus diameter (Figs. 15–16). Rest of head similar to female. Mesosoma. Similar to female, except rugosity of propodeal triangle more extensive, covering basal third of triangle; tarsal claws bidentate. Metasoma. Similar to female. Genitalia and hidden sterna (Fig. 17). Dorsal gonocoxite lobe distinct, rounded. Gonostylus blade strongly broadened, more or less triangular, flattened, outer margin weakly concave, inner margin strongly convex, apex rounded. Penis valves moderately broad basally, tapering apically (Fig. 17). Sternum 8 narrow, columnar, apical process broadened, apical margin distinctly notched, fishtail-shaped. Diagnosis. Andrena curviocciput is easily differentiated from all other species of Aciandrena by the strongly arched vertex, with the lateral ocelli reaching the preoccipital ridge, therefore without an ocelloccipital distance; this is especially pronounced in the female (Figs. 11, 12, 15, 16). Andrena pulicaria Warncke also possesses a strongly arched vertex, but differs in the distinct ocelloccipital distance, stronger shagreenation on mesonotum and terga, longer female clypeus which is smooth apically, and centrally yellow male clypeus. Distribution: High altitudes in Lebanon, southeast Turkey and northern Israel (Mt. Hermon). Likely present also in Syria. Flight period: April–June. Flower records: Brassicaceae spp. Holotype: ISRAEL: Mount Hermon [Hermon], 1640–1675 m, 33.298–299°N 35.767–770°E, 19.v.2022, G. Pisanty, on Brassicaceae, ♀ (SMNHTAU:392774). Paratypes: ISRAEL: Hermon Nature Reserve [Hermon NR], 300 m N lower parking lot, 1508 m, 33.294°N 35.760°E, 28.v.2019, L. Friedman (1♀); Mount Hermon [Har Hermon], 1500 m, 25.v.1977, D. Gerling (1♀); 1600 m, 23.v.1998, A. Freidberg (1♀); 18.v.2009, A. Freidberg (1♀); 33.300°N 35.767°E, 11.v.2020, G. Pisanty, pan traps (2♀, 1♂); 33.3005°N 35.767°E, 15.v.2016, G. Pisanty, pan trap (1♀); 1620 m, 33.300ºN 35.767ºE, 11.v.2020, G. Pisanty (1♂); 1642 m, 33.2992°N 35.7668°E, 19.v.2022, G. Pisanty, pan trap (1♀); 1659 m, 33.2984°N 35.7683°E, 19.v.2022, G. Pisanty, pan trap (1♀); 1970 m, 33.310°N 35.796°E, 15.v.2016, G. Pisanty, pan trap (1♀); [Hermon], 1640–1675 m, 33.298–299°N 35.767–770°E, 19.v.2022, G. Pisanty, sweeping (7♀) and on Brassicaceae (2♀); LEBANON: Tannourine, 28.iv.2016, N. Nemer (1♂); TURKEY: Karadut, Nemrut Dag, 9.vi.1998, M. Halada (2♀); Nemrut Dağı, Adiyaman, 1500 m, 1.vi.1983, K. Warncke (1♀); Tanin-Tanin-Pass, 2300 m, 19.v.1989, K. Warncke (1♂) (OLML, RMNH, SMNHTAU, TJW). Etymology. curviocciput = Latin for the “curved occiput” characteristic of this species, with an extremely small ocelloccipital distance. The species epithet is a noun in apposition., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 15-16, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826
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45. Andrena (Notandrena) deserta Warncke 1974
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Andrena deserta ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Notandrena) deserta Warncke, 1974 Distribution: Algeria, Israel (first record), Tunisia. Flight period: February–March (Warncke 1974a). Flower records: Brassicaceae: Erucaria microcarpa. Material examined: HOLOTYPE: ALGERIA: Biskra, 1.iii.1897 (♀) (OLML); PARATYPE: TUNISIA: Gafsa (1♂) (OLML); non-type material: ALGERIA: Tiaret, Bougara, 15.iv.2018, A. Dermane (2♀); 22.iv.2018, A. Dermane (1♀, 1♂); ISRAEL: Mashabei Sadeh [Mash’abbe Sade], 23.ii.1979, D. Furth (1♀); Tel Yeroham, 25.iii.1959, I. Kugler, on Erucaria microcarpa (3♂); Yeruham [Yeroham], 24.iii.1959, I. Kugler (1♀) (AD, SMNHTAU, TJW)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 60, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Warncke, K. (1974 a) Beitrag zur Kenntnis und Verbreitung der Sandbienen in Nordafrika (Hymenoptera, Apoidea, Andrena). Mitteilungen aus dem Zoologischen Museum in Berlin, 50, 2 - 53."]}
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46. Andrena (Micrandrena) minutula
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy ,Andrena minutula - Abstract
Andrena (Micrandrena) minutula (Kirby, 1802) Distribution: North-western Africa, through Europe to Cyprus, Turkey and Lebanon (Gusenleitner & Schwarz 2002; Wood et al. 2020a). Remarks. Zavattari (1905) mentions this species (as A. parvula Kirby) from Jericho, which is unlikely, given the northern distribution of A. minutula in the Levant. The mountain ranges of Lebanon seem to be the southernmost distributional limit of A. minutula in this region (Wood et al. 2020a). This questionable record could refer to another species of Micrandrena (e.g. A. spreta Pérez), as most of the species concepts of Micrandrena did not exist at the time of this publication., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 102, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Kirby, W. (1802) Monographia Apum Angliae. II. Privately published, Ipswich, 388 pp.","Gusenleitner, F. & Schwarz, M. (2002) Weltweite Checkliste der Bienengattung Andrena mit Bemerkungen und Erganzungen zu palaarktischen Arten (Hymenoptera, Apidae, Andreninae, Andrena). Entomofauna, Supplement 10, 1 - 1280.","Wood, T. J., Boustani, M. & Rasmont, P. (2020 a) A revision of the Andrena (Hymenoptera: Andrenidae) of Lebanon with the description of six new species. Annales de la Societe Entomologique de France, 56, 279 - 312. https: // doi. org / 10.1080 / 00379271.2020.1794960","Zavattari, E. (1905) Viaggio del Dr. E. Festa in Palestina, nel Libano e regiorii vicine. XVI. Imenotteri. Bollettino dei Musei di Zoologia ed Anatomia Comparata della Reale Universita di Torino, 20 (518), 1 - 10. https: // doi. org / 10.5962 / bhl. part. 9304"]}
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47. Andrena (Truncandrena) noacki Alfken 1935
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Andrena noacki ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Truncandrena) noacki Alfken, 1935 sp. resurr. (Fig. 179) Andrena noacki Alfken, 1935 Andrena oulskii noacki: Warncke 1967 Andrena oulskii Radoszkowski, 1867: Gusenleitner & Schwarz 2001, 2002 Distribution: Turkey. Flight period: May–June (Hazir et al. 2014). Material examined: HOLOTYPE: TURKEY: Ankara, 1.vi.1934, A. Seitz (♀) (SMFM); PARATYPES: TURKEY: same as holotype (2♀) (ZMHB). Remarks. Members of the Truncandrena with orange tarsi have been greatly confused; Warncke adopted a lumping approach and united most taxa (as subspecies) under either A. minapalumboi Gribodo or A. oulskii Radoszkowski. Subsequent authors have reinstated some of these names such as A. delphiensis Warncke (Greece, Gusenleitner & Schwarz 2002) or simply used them as good taxa (Hazir et al. 2014). Though confused (Schuberth et al. 2001), the use of the name A. oulskii was stabilised as a Truncandrena species by Wood (2021b). It is therefore necessary to reinstate the taxa A. noacki and A. ochraceohirta Alfken from their Warncke baseline of synonymy with A. oulskii and A. minapalumboi (Gusenleitner & Schwarz 2002). These changes bring the taxonomic baseline into line with current use of these names and concepts (Hazir et al. 2014). Andrena noacki has dark terga and complete hair bands on terga 1–2 (Fig. 179), whereas A. oulskii has redmarked terga (Fig. 181), and in A. ochraceohirta sp. resurr. and A. oulskii the hair bands on terga 1–2 are always interrupted (Figs. 180–181). The latter character is independent of the age of the specimen, as fresh A. ochraceohirta never have complete hair bands on terga 1–2, so it is not the result of abrasion. Andrena noacki is currently known only from the Central Anatolian plateau of Turkey, and is therefore isolated from A. ochraceohirta in the southern Levant.
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48. Andrena (Micrandrena) dividicincta Pisanty & Scheuchl & Martin & Cardinal & Wood 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena dividicincta ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Micrandrena) dividicincta Pisanty sp. nov. (Figs. 102–109) Female (Fig. 102). Body length: 7–7.5 mm. Colour. Body dark brown (Fig. 102). Flagellum entirely dark brown. Femora, tibiae and basitarsi dark brown; apical tarsal segments reddish-brown. Wings slightly infuscate, veins brown, stigma orangish-brown (Fig. 102). Tergal marginal zones light to dark brown (Fig. 105). Pubescence. Head and mesosoma covered with whitish to light brown plumose hairs of moderate length and density (Figs. 102–104). Facial fovea with dense, minute brownish hairs (Fig. 104). Propodeal corbicula incomplete, posterodorsal fringe with long plumose hairs. Surface of corbicula with few long simple hairs. Leg hair whitish-golden (Fig. 102). Flocculus incomplete. Scopal hairs mostly simple, unilaterally plumose on posterior part. Surface of tergal discs almost bare medially, with very sparse, short bright hairs laterally. Tergal marginal zones 2-4 with distinct interrupted bands of very dense white hairs, covering 1/2–2/3 of tergal width. Terminal fringe golden (Fig. 105). Head (Figs. 103–104). 1.1 times broader than long. Galea shiny, superficially shagreened. Labral process broad and short, more or less arched. Clypeus very weakly convex, almost flat, shagreened basally, shagreened to smooth apically, distance between punctures 1–1.5 puncture diameters, puncture size medium, without impunctate midline (Fig. 103). Paraocular area strongly punctate below, strongly longitudinally grooved above. Supraclypeal area weakly punctate to longitudinally grooved. Flagellomere 1 about as long as 2+3, 2 as long as 3 or slightly shorter. Frons strongly longitudinally striated, with an areolate midline. Facial fovea narrow, almost linear, extending from level of medial ocellus to base of clypeus, 0.4 times as broad as antennocular distance, distinctly separated from compound eye (Figs. 103–104). Distance of fovea from lateral ocellus about 2 ocellus diameters. Ocelloccipital distance 1 ocellus diameter. Vertex carinate (Fig. 104). Mesosoma (Fig. 104). Dorsolateral angle of pronotum not to very weakly elevated, pronotum not carinate laterally. Mesonotum entirely matt and strongly shagreened, coarsely but very shallowly, obliquely punctured, punctures visible mostly in anterior view, distance between punctures 1–2 puncture diameters. Scutellum similar, slightly shinier (Fig. 104). Mesepisternum matt, finely alveolate, impunctate, anterior part weakly rugose-areolate. Propodeal triangle finely rugose-areolate mediobasally, alveolate apicolaterally (Fig. 104). Posterolateral part of propodeum finely alveolate, impunctate, sculpturing finer compared to triangle. Propodeal corbicula shiny, finely reticulated, impunctate. Hind leg pretarsal claws distinctly bidentate. Submarginal crossvein 1 reaching marginal cell 1–2 vein widths from stigma. Recurrent vein 1 reaching marginal cell 2 at its middle or proximal to it. Nervulus interstitial to very weakly antefurcal. Metasoma (Fig. 105). Tergal discs moderately to weakly shagreened, somewhat shiny, impunctate, shagreenation strongest on tergum 2 and weakest on 3–4. Tergal marginal zones weakly depressed, basal part more weakly shagreened than disc, apical part smooth. Male (Fig. 106). Body length. 6 mm. Colour. Similar to female. Clypeus and paraocular areas dark (Fig. 107). Pubescence. Head and mesosoma with long, plumose, mostly yellowish hair (Figs. 106–107). Frons, lateral part of paraocular area, and upper part of genal area with short to medium dark hairs (Figs. 106–107). Metasomal hair similar to female, but terminal fringe whitish (Fig. 108). Head (Fig. 107). 1.2 times broader than long. Clypeus almost flat, very smooth and shiny, strongly and densely punctate, distance between punctures 0.5–2 puncture diameters, puncture density increasing laterally, without impunctate midline. Flagellomere 1 slightly shorter than 3, 2 slightly shorter than 1 (Fig. 107). Rest of head similar to female. Mesosoma. Similar to female. Metasoma (Fig. 108). Tergal disc 1 shiny, very superficially shagreened, weakly, sparsely and very finely punctate, distance between punctures 2 puncture diameters. Tergal discs 2–5 shagreened basally and smooth apically, shagreenation decreasing gradually towards distal terga, punctation weak, sparse and very fine, distance between punctures 2–3 puncture diameters. Tergal marginal zones weakly depressed, smooth to very slightly shagreened, impunctate. Genitalia and hidden sterna (Fig. 109). Gonocoxites separated almost from base, dorsal gonocoxite lobe strongly developed, rounded. Gonostylus blade strongly and abruptly broadened apically. Penis valves broad basally, strongly tapering apically (Fig. 109). Sternum 8 simple, columnar, narrow, apical process spatulate, not broadened. Diagnosis. Andrena dividicincta is closely related to A. querquedula Warncke from Turkey, and both species are easily distinguished from most Micrandrena by the almost flat clypeus, impunctate female terga, broad and finely granular propodeal triangle, and unique pattern of metasomal hair bands. Andrena dividicincta differs from A. querquedula in the stronger shagreenation of the male clypeus (smooth in A. querquedula) and female and male terga (completely smooth in female A. querquedula, and to a lesser extent in the male). Distribution: Northern Israel (Upper Galilee and Mount Hermon). Likely present also in Lebanon and Syria. Flight period: February–April. Flower records: Rosaceae: Prunus dulcis, Pyrus syriaca; Sapindaceae: Acer monspessulanum. Pollen analysis. Six analysed pollen loads from Mount Hermon, Montfort and Meron Junction contained 31.2% Sapindaceae (Acer), 30.6% Rosacaeae (Prunus - type, Crataegus - type), 19.0% Rhamnaceae (Rhamnus - type), and 19.0% an unidentified, featureless pollen type (Poaceae?). The species therefore appears to be polylectic, favouring flowering trees and shrubs. Holotype: ISRAEL: Montfort, Nahal Kziv [Montfort, Nahal Keziv], 28.ii.2018, G. Pisanty, ♀ (SMNHTAU:286301). Paratypes: ISRAEL: Meron Junction [Meron JNC.], 20.iii.1995, on Pyrus syriaca (9♀); Montfort, 2.iii.1987, A. Freidberg (1♀) and A. Shlagman (1♀); 4.iii.1993, A. Freidberg (2♀); 5.iii.2008, A. Freidberg (1♀); [Monfort], 10.iii.1981, F. Kaplan (1♀); [Montfort, Nahal Keziv], 28.ii.2018, G. Pisanty (3♀, 1♂); [Nahal Keziv, Montfort], 400 m, 33°02’N 35°14’E, 24.ii.2011, A. Freidberg (1♀); Mount Hermon [Har Hermon], 1644 m, 33.2992°N 35.7670°E, 16.iv.2022, G. Pisanty, pan trap (1♀); 1649 m, 33.2993°N 35.7679°E, 7.iv.2021, G. Pisanty, pan trap (2♂), sweeping (2♀), and on Acer monspessulanum (12♀, 1♂); 16.iv.2021, G. Pisanty, on Acer monspessulanum (87♀, 2♂); 1650 m, 33.2993°N 35.7678°E, 16.iv.2022, G. Pisanty, on Acer monspessulanum (16♀, 2♂); [Hermon], 1641 m, 33.2993°N 35.7670°E, 16.iv.2022, G. Pisanty, on Prunus dulcis (7♀); 1642 m, 33.2992°N 35.7668°E, 16.iv.2022, G. Pisanty, on Rosaceae (11♀); Mount Meron [Har Meron], 800 m, 5.iii.2011, A. Freidberg (1♂); Nahal Kziv [Nahal Keziv], 33°02.7’N 35°13.6’E, 5.iii.2008, A. Freidberg (1♀); 33.0465°N 35.226°E, 26.ii.2021, G. Pisanty (1♀); Sasa, 20.iv.2015, O. Winberger (1♀) (ES, NHMUK, OLML, RMNH, SMNHTAU, TJW, ZMHB, ZSMC). Etymology. dividicincta = Latin for “with divided belt”, in reference to the species’ strongly interrupted tergal hair bands. The species epithet is an adjective. Other material examined (A. querquedula): PARATYPES: TURKEY: Akseki / Taurus, 1300 m, 25.iv.1973, K. Warncke (2♀, 10♂) (SMNHTAU).
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49. Andrena (Aciandrena) varicornis Perez 1895
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena varicornis ,Andrena ,Animalia ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Aciandrena) varicornis Pérez, 1895 (Fig. 44) Distribution: Algeria, Egypt, southern Israel, Morocco, Tunisia, West Bank (Wood et al. 2020b). Flight period: February–April. Flower records: Brassicaceae: Sisymbrium irio. Material examined: ISRAEL: Har Horesha, Rt. 171, 930 m, 2.iv.2014, L. Friedman (2♀); Holot Mash’abbim Nature Reserve [Holot Mash’abbim], 30.999°N 34.7578°E, 18.ii.2022, G. Pisanty (1♂); Nahal Sayif, 14.iv.2007, Y. Hollander (1♀); Nahal Zin, 15.iv.2007, I. Lalzar (1♀); Sde Boker, 22.iii.1963, J. Kugler (1♂); Shivta, 17.iii.1977, A. Freidberg (2♀, 1♂); Shivta junction, 30.941°N 34.597°E, 10.iii.2017, G. Pisanty (1♂); Yeruham [Bir Rekhme], 21.iii.1958, L. Fishelsohn (1♀); WEST BANK: Nabi Musa Road, 22.ii.2014, A. Gotlieb, on Sisymbrium irio (1♀) (SMNHTAU). Remarks. The integumental colour of terga 2–5 in Israeli A. varicornis females varies from the typical brown to reddish (specimens from Har Horesha, Nahal Sayif, Nabi Musa Road)—a variant hitherto unknown from North African populations (Fig. 44)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on page 26, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Perez, J. (1895) Especes nouvelles de Melliferes de Barbarie. (Diagnoses preliminaires). Gounouilhou, Bordeaux, 64 pp.","Wood, T. J., Michez, D., Cejas, D., Lhomme, P. & Rasmont, P. (2020 b) An update and revision of the Andrena fauna of Morocco (Hymenoptera, Apoidea, Andrenidae) with the description of eleven new North African species. Zookeys, 974, 31 - 92. https: // doi. org / 10.3897 / zookeys. 974.54794"]}
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50. Andrena (Euandrena) gageae Wood & Pisanty 2022, sp. nov
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Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie, and Wood, Thomas James
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Andrenidae ,Insecta ,Arthropoda ,Andrena ,Animalia ,Andrena gageae ,Biodiversity ,Hymenoptera ,Taxonomy - Abstract
Andrena (Euandrena) gageae Wood & Pisanty sp. nov. (Figs. 78–85) Female (Fig. 78). Body length: 9–10 mm. Colour. Body black (Fig. 78). Flagellum black basally, flagellomeres 3–10 ventrally lightened by presence of grey cilia. Apical tarsal segments very slightly lightened brown. Wings hyaline, stigma and venation dark orange to orange (Fig. 78). Tergal marginal zones apically lightened brown-hyaline (Fig. 81). Pubescence. Face, paraocular area and gena with black hairs (Figs. 78–80). Gena immediately behind base of mandibles with tuft of long white hair intermixed among black hairs. Vertex with almost entirely long white hairs. Frons and area around antennal sockets with mixture of black and white hairs (Fig. 79). Mesonotum and scutellum with long white hairs (Figs. 78, 80). Mesepisternum predominantly with long black hairs, mixing with white hairs anterolaterally and ventrally (Fig. 78). Propodeal corbicula incomplete, composed predominantly of black plumose hairs with occasional white hairs intermixed. Surface of corbicula with sparse simple whitish hairs. Leg hair blackish brown, femoral scopa white, tibial scopa whitish golden (Fig. 78). Flocculus incomplete, composed of sparse black plumose hairs. Tergum 1 with long sparse white hairs, 2–3 with short white hairs on discs. Terga 2–3 laterally, 4–5 all over with black hairs. Terminal fringe dark brown (Fig. 81). Head (Figs. 79–80). 1.3 times broader than long. Labral process short, trapezoidal, basally 3 times broader than long, apical margin straight. Clypeus flattened centrally, strongly and evenly punctured, punctures separated by 0.5 puncture diameters laterally, becoming slightly sparser centrally, here separated by 1 puncture diameter. Clypeal surface smooth and shining over majority of its area except for narrowly shagreened area basally (Fig. 79). Paraocular area with clear punctures of same density as on clypeus, frons finely longitudinally ridged, dull. Flagellomere 1 exceeds 2+3, shorter than 2+3+4. Facial fovea dorsally occupying 0.25 distance between lateral ocellus and compound eye, narrowed below at level of antennal insertions, here narrower than width of flagellum (Figs. 79–80). Fovea dorsally separated from lateral ocellus by 2.5 diameter of lateral ocellus. Ocelloccipital distance subequal to width of lateral ocellus (Fig. 80). Genal area slightly exceeding width of compound eye. Mesosoma (Fig. 80). Pronotum with very subtly elevated dorsolateral angle, essentially rounded. Mesonotum and scutellum laterally shagreened and dull, this becoming weaker centrally, here weakly shining to shining; irregularly punctured with shallow punctures, punctures separated by 0.5–2 puncture diameters (Fig. 80). Mesepisternum and propodeal corbicula finely reticulate, weakly shining. Propodeal triangle narrow, internal surface centrally and laterally with network of fine raised rugosity, otherwise with fine granular microreticulation; lateral margins of propodeal triangle differentiated from dorsolateral parts of propodeum by change in sculpture, dorsolateral parts granularly shagreened with fine network of raised reticulation (Fig. 80). Tarsal claws with strong inner tooth. Recurrent vein 1 reaching submarginal cell 2 very slightly before its middle. Submarginal crossvein 1 meets marginal cell 5 vein widths from stigma. Nervulus interstitial to slightly antefurcal (Fig. 78). Metasoma (Fig. 81). Tergal discs with variable sculpturing, tergum 1 with disc and declivity smooth and shining, 2–4 with discs smooth centrally to shagreened basally; all terga with fine and sparse punctures, punctures separated by 3–5 puncture diameters. Tergal margins weakly depressed, occupying 0.3–0.4 of tergal width, with fine latitudinal granular shagreen. Pygidial plate pointed triangular, centrally slightly raised, densely punctate. Male (Fig. 82). Body length: 8 mm. Colour. As in the female. Pubescence. Similar to female. Gena and base of mandibles with larger, more extensive patch of intermixed white hairs, extending to flank galea laterally in frontal view. Intermixed white hairs of face more extensive, a few extending onto base of clypeus (Fig. 83). Mesepisternum with white hairs more extensive, extending dorsally to mid-way point. Terga lacking dark hairs, entirely white-haired (Fig. 82). Head (Figs. 83–84). 1.3 times broader than long. Structurally as in the female, though flagellomere 1 exceeding 2, shorter than 2+3. Mesosoma (Fig. 84). Structurally as in female, though shining central area of mesonotum comparatively small (Fig. 84). Nervulus clearly antefurcal. Metasoma. As in female. Genitalia and hidden sterna (Fig. 85). Genital capsule with gonocoxa produced into small teeth, apically touching. Gonostyli flattened, with weakly raised internal margin, apically spatulate. Penis valves basally slightly broadened, narrowing medially before slightly broadened and drop-like apex (Fig. 85). Sternum 8 columnar, slightly broadened apically, essentially parallel sided, apically truncate. Ventral surface with short brownish hairs projecting laterally. Diagnosis. Andrena gageae can be placed in the subgenus Euandrena because of the characteristic drop-shaped fovea which are narrowed below, and the simple scopal hairs. Further diagnosis is highly challenging and ideally requires comparison with barcoded specimens. Females have a similar hair colour pattern to A. bicolor Fabricius, but have white hairs on the face, the clypeus is flattened centrally and the surface is smooth and shining, and the terga are smoother with finer and sparser punctation. There are similarities to A. glabriventris Alfken known from Turkey which has the same hair colour pattern (though without intermixed pale hairs on the face), but can be separated structurally because the vertex of A. glabriventris females behind the ocellar triangle is densely punctate, whereas it is impunctate in A. gageae. Females are identical to the description of A. hermonella Scheuchl & Pisanty females. However, this is because the sexes of A. hermonella were incorrectly associated. The male of A. gageae (confirmed by barcoding, Table 2) which was caught at the same locality on the same day has simple, ‘typical’ Euandrena genitalia, without the lateral hyaline extensions to the penis valves that characterise A. hermonella (see illustrations in Pisanty et al. 2016). The tergal punctation of the A. gageae male is also much less dense, further supporting this difference. Males can therefore be diagnosed by the combination of white hairs on the face, smooth and sparsely punctate terga, and simple genital capsule. Distribution: Israel and Lebanon, from high altitude (> 2000 m) in the Mount Lebanon and Anti-Lebanon mountain chains. Likely present also in Syria. Flight period. May, presumably into June. Flower records. Lilaceae: Gagea micrantha. Pollen analysis. Five analysed pollen loads contained pure Gagea pollen. However, pollen loads were all from the same day, so caution should be taken before interpreting these results as representative of the entire diet. Other alpine Euandrena can show affinity with other monocotyledon plants whilst also having a generalised diet (Praz et al. 2019). Holotype: LEBANON: Bsharri [Bcharré], Dahr el Adib, 2585 m, 34 o 12’40.0”N, 36 o 03’35.7”E, 27.v.2017, P. Rasmont & M. Boustani, ♀ (OLML). Paratypes: ISRAEL: Mount Hermon, 2000 m, 22.v.1973, H. Bytinski-Salz (1♀); 2050 m, 31.v.1991, K. Warncke (2♀) (A. hermonella paratype labels); LEBANON: Bsharri [Bcharré], Dahr el Adib, 2585 m, 34 o 12’40.0”N, 36 o 03’35.7”E, 27.v.2017, P. Rasmont & M. Boustani, (6♀, 1♂) (OLML, SMNHTAU, TJW). Etymology. Named after the yellow star-of-Bethlehem lily Gagea micrantha. The species epithet is an adjective. Remarks. There is a swarm of Euandrena diversity in southeastern Europe to the Levant (Praz et al. 2019; GP, TJW and C. Praz, unpublished data), much of it probably undescribed. Extreme care must be taken when determining Euandrena in this region; barcoding specimens is essential.A further publication will resolve outstanding issues in East Mediterranean members of this subgenus. Lebanese specimens were collected from Gagea micrantha which may be important for its ecology in the way that other monocotyledon plants are for other species of alpine Euandrena (Praz et al. 2019). This plant taxon is also restricted to Israel, Lebanon and Syria in high altitude sites. Other material examined: (A. glabriventris): HOLOTYPE: TURKEY: Ankara, 10.v.1934, A. Seitz (♀) (SMFM); PARATYPES: TURKEY: same as holotype (3♀) (SMFM)., Published as part of Pisanty, Gideon, Scheuchl, Erwin, Martin, Teresa, Cardinal, Sophie & Wood, Thomas James, 2022, Twenty-five new species of mining bees (Hymenoptera: Andrenidae: Andrena) from Israel and the Levant, pp. 1-109 in Zootaxa 5185 (1) on pages 37-40, DOI: 10.11646/zootaxa.5185.1.1, http://zenodo.org/record/7073826, {"references":["Pisanty, G., Scheuchl, E. & Dorchin, N. (2016) Eight new species of Andrena Fabricius (Hymenoptera: Apoidea: Andrenidae) from Israel - a Mediterranean hotspot for wild bees. Zootaxa, 4189 (3), 485 - 515. https: // doi. org / 10.11646 / zootaxa. 4189.3.3","Praz, C., Muller, A. & Genoud, D. (2019) Hidden diversity in European bees: Andrena amieti sp. n., a new Alpine bee species related to Andrena bicolor (Fabricius, 1775) (Hymenoptera, Apoidea, Andrenidae). Alpine Entomology, 3, 11 - 38."]}
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