FIGURES 45-50 - uploaded by Thomas James Wood
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Andrena rubricorpora spec. nov. 45. female profile, 46. female face, 47. female face detail, 48. female scutum, 49. female tibial scopa, 50. female terga. PARATYPE: TUNISIA: Same as holotype, 1♀ (OÖLM). Description: Female: Body length 10 mm (Figure 45). Head: Black, 1.1 times longer than wide (Figure 46).
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Andrena is the second most speciose genus of bees, with around 1,500 species known globally. It is predominantly distributed through the Holarctic with severely limited diversity in other biogeographical regions, and with the greatest species richness in arid and Mediterranean areas. Despite a long history of study, many species remain undescribed....
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... Because most andrenids (in particular, the majority of Andrena species) are spring-flying bees, their underrepresentation could be related to sampling periods focusing more on summer months, or due to lack of spring-flowering forage in gardens (Matteson et al., 2008). Global totals for Andrenidae are also enhanced by a uniquely large radiation of perditine (genera Perdita and Macrotera) and protandrenine (Protandrena sensu lato) in deserts and of Andrena in Mediterranean areas (Wood, 2021;Bossert et al., 2022). All but four of the garden bee studies included in this review were from different regions and/or biomes less favorable to this family (Table 1). ...
Urban garden spaces are potentially important habitats for bee conservation. Gardens can host diverse flora, which provide floral resources across foraging seasons for bee species. Recent reviews have focused on the impacts of cityscapes on urban bee assemblages in different green spaces. Urban gardens are distinct from other urban green spaces, and bee communities in urban spaces have been an increasing topic of study over the past few decades. We reviewed 28 urban garden bee studies spanning five decades and 14 countries to compile an original metadataset of bee species' functional traits to understand the conservation value of gardens, identify gaps in bee sampling efforts, and summarize the calls to action included by their authors. Studies of urban garden bees have documented between 674 (conservative count, excluding morphospecies) and 830 (liberal count, including morphospecies) bee species. Urban garden bee communities were taxonomically and functionally diverse, although bee species that were non-eusocial, ground-nesting, generalist foragers, and native were most common in garden habitats. The proportion of parasitic bee species and specialist foragers found in urban gardens was comparable to proportions for global bee taxa. This suggests that gardens contain the hosts and forage needed to support bees with specialized life history requirements, and thus represent high quality habitat for a subset of bee communities. Garden bee research was strongly biased toward the northern hemisphere, which signifies a large gap in our understanding of garden bee communities in other regions. The variety of, and non-standard sampling methods in garden bee research makes it difficult to directly compare results between studies. In addition, both intentional low taxonomic resolution and a lack of collaboration with taxonomists constrains our understanding of bee diversity. Our analyses highlight both successes of past urban garden bee studies, and areas of opportunity for future research as we move into a sixth decade of garden bee research.
... Southern Europe, Turkey, the Caucasus, Iran, Turkmenistan Osytshnjuk et al. 2008). Literature records Wood (2021a). ...
... While it is still too soon to discuss faunal affinities in depth given the high diversity of Andrena of the Middle Eastern region, which is still being actively described (Pisanty et al. 2016Wood et al. 2020a;Wood 2021a), some clear trends can be seen. The first is that there is a clear link between the Anti-Lebanon mountain range, the mountains of south and south-eastern Turkey (predominantly in Hakkâri Province), and the Zagros Mountains of Iran. ...
Iran is a huge but understudied Middle Eastern country with a rich but chronically understudied bee fauna, including for the highly-speciose bee genus Andrena. Examination of unidentified museum material combined with recent field collections and a critical review of the literature has revealed a total of 197 species of Andrena in the Iranian fauna, of which 65 are newly reported for the country, with an additional 16 species new for science. Andrena (Aciandrena) deminuta Wood sp. nov., Andrena (Euandrena) boustaniae Wood sp. nov., Andrena (Euandrena) oblata sp. nov., Andrena (Euandrena) sani sp. nov., Andrena (Micrandrena) elam Wood sp. nov., Andrena (Micrandrena) subviridula Wood sp. nov., Andrena (Notandrena) idigna Wood sp. nov., Andrena (Planiandrena) flagrans Wood sp. nov., Andrena (Planiandrena) sella Wood sp. nov., Andrena (Ulandrena) bulbosa Wood sp. nov., Andrena (incertae sedis) hosseiniiae Wood & Monfared sp. nov., and Andrena (incertae sedis) rostamiae sp. nov. are described from Iran, Andrena (Micrandrena) extenuata sp. nov. is described from Iran and Syria, Andrena (Micrandrena) tabula Wood sp. nov. and Andrena (Micrandrena) obsidiana Wood sp. nov. are described from Iran and Turkey, and Andrena (Planiandrena) huma sp. nov. is described from Iran, Syria, and the Golan Heights. Eight taxa are synonymised (valid name first): Andrena (Melandrena) assimilis Radoszkowski, 1876 = Andrena (Melandrena) gallica Schmiedeknecht, 1883 syn. nov.; Andrena (Notandrena) emesiana Pérez, 1911 stat. resurr. = Andrena (Notandrena) recurvirostra Warncke, 1975 syn. nov.; Andrena (Plastandrena) eversmanni Radoszkowski, 1867 = Andrena (Plastandrena) peshinica Nurse, 1904 syn. nov.; Andrena (incertae sedis) hieroglyphica Morawitz, 1876 = Andrena (Carandrena) cara Nurse, 1904 syn. nov. and Andrena (Carandrena) halictoides Nurse, 1904 syn. nov.; Andrena (Melandrena) induta Morawitz, 1894 = Andrena (Melandrena) patella Nurse, 1903 syn. nov.; Andrena (incertae sedis) minor Warncke, 1975 stat. nov. = Andrena (Carandrena) splendula Osytshnjuk, 1984 syn. nov.; Andrena (Notandrena) zostera Warncke, 1975 = Andrena (Carandrena) subsmaragdina Osytshnjuk, 1984 syn. nov. Overall, these results considerably improve our understanding of the Iranian Andrena fauna, and suggest that overall bee diversity in this country is substantially more than 1000 species.
... Given the many outstanding issues with Andrena subgeneric classification despite many recent advances in our understanding of this huge genus (PISANTY et al., 2021), many problems persist. Given the large numbers of species that continue to be described from poorly studied parts of the Mediterranean basin (PISANTY et al., 2016;WOOD et al., 2021;WOOD, 2021), new taxa may be discovered that join the apparent distributional gap between species tentatively placed in the subgenus Planiandrena. Alternatively, as cutting-edge genetic techniques become more available, phylogenetic studies will be able to more accurately place obscure, overlooked, and poorly-studied species (e.g. ...
Iberia has a species-rich bee fauna as a result of its predominantly Mediterranean climate and the diversity of habitats that can be found across the peninsula. One region that displays some of this habitat diversity are the Doñana natural areas in south-western Spain. Though it is known to host species with highly restricted Iberian or Atlantic distributions, many of these have only been discovered or described recently, suggesting that the area would benefit from more focused surveys. Targeted bee surveys of the Doñana Protected Areas detected 51 species of Andrena, including one new species for science, Andrena (?Planiandrena) ramosa sp. nov. Surprisingly, this taxon shows greatest affinity with a small group of species known from Central Asia rather than any known West Mediterranean taxa. These results illustrate the local faunal richness present in Doñana, as well as re-emphasising the need for additional targeted surveys in order to fully document bee diversity in southern Europe.
North-western Africa has a large Andrena fauna, but parts of the country away from coastal areas remain poorly studied, and confusion persists as to the identity of certain taxa due to the long history of study combined with imperfectly examined type material. New fieldwork, genetic barcoding, and study of museum material has substantially improved our understanding of this region. Eleven new species are described: A. (Aciandrena) bendai sp. nov., A. (Aciandrena) ifranensis sp. nov., A. (Euandrena) berberica sp. nov., A. (Hoplandrena) darha sp. nov., A. (Micrandrena) anammas sp. nov., A. (Micrandrena) gemina sp. nov., A. (Micrandrena) tinctoria sp. nov., and A. (incertae sedis) muelleri sp. nov., all from Morocco, and A. (Aciandrena) quieta sp. nov., A. (Euandrena) abscondita sp. nov., and A. (Taeniandrena) prazi sp. nov. from Morocco and Tunisia. Andrena (Aciandrena) nitidilabris Pérez, 1895 was misdiagnosed, and is actually the senior synonym of A. (Graecandrena) montarca parva Warncke, 1974 syn. nov. Andrena (Aciandrena) pisantyi sp. nov. is described from Algeria, Tunisia, and Israel, conforming to A. nitidilabris auctorum sensu Warncke. Andrena (Graecandrena) andina Warncke, 1974 stat. nov. and A. (Micrandrena) heliaca Warncke, 1974 stat. nov. are elevated from sub species to species status. Lectotypes are designated for A. (Melanapis) ephippium Spinola, 1838, A. (Melanapis) rutila Spinola, 1838, A. (Simandrena) rhypara Pérez, 1903, and A. (Suandrena) savignyi Spinola, 1838. Neotypes are designated for A. (Melandrena) soror Dours, 1872 and A. (Notandrena) nigroviridula Dours, 1873. The female of A. (Aciandrena) triangulivalvis Wood, 2020 is described. The following seven additional synonymies are reported (senior name first): A. (Chrysandrena) testaceipes Saunders, 1908 = A. (Chrysandrena) rubricorpora Wood, 2021 syn. nov., A. (incertae sedis) maidaqi Scheuchl & Gusenleitner, 2007 = A. (Carandrena) hoggara Wood, 2021 syn. nov., A. (Lepidandrena) tuberculifera Pérez, 1895 = A. (Poecilandrena) nigriclypeus Wood, 2020 syn. nov., A. (Notandrena) albohirta Saunders, 1908 = A. (Notandrena) eddaensis Gusenleitner, 1998 syn. nov., A. (Notandrena) microthorax Pérez, 1895 = A. (Notandrena) nigrocyanea Saunders, 1908 syn. nov., A. (Simandrena) rhypara = A. (Simandrena) palumba Warncke, 1974 syn. nov., and A. (Taeniandrena) poupillieri Dours, 1872 = A. (Taeniandrena) lecerfi Benoist, 1961 syn. nov. Andrena (Notandrena) viridiaenea Pérez, 1903 is returned to synonymy with A. nigroviridula. Relative to the 2020 baseline, 16 Andrena species are newly recorded for Morocco, and six species are removed from the faunal list. These revisions bring the total number of Andrena species known from Morocco to 202 with 25 endemic species, making it one of the hotspots for Andrena diversity globally.
The Iberian Peninsula is a global hotspot for bee diversity due to its large number of different habitats, particularly Mediterranean scrubland, mountains, and hot and cold steppe. In line with its status as a hotspot of bee diversity, the peninsula hosts a very large Andrena fauna, which despite progress in recent years remains incompletely studied, particularly with reference to genetic investigation. Here the Iberian Andrena fauna is comprehensively revised, resulting in a total of 228 recorded species. Numerous taxonomic changes are necessary following inspection of museum specimens, type material, and genetic investigation. The following subgenera are described: Pruinosandrena subgen. nov. , containing six taxa previously placed in the subgenus Campylogaster Dours, 1873, and Blandandrena subgen. nov. , Bryandrena subgen. nov. , Limbandrena subgen. nov. , and Ovandrena subgen. nov. , containing one, one, one, and four taxa previously placed in the subgenus Poliandrena Warncke, 1968. Andrena (Limbandrena) toelgiana Friese, 1921 syn. nov. is synonymised with A. (Limbandrena) limbata Eversmann, 1852. The current lectotype of A. (Micrandrena) obsoleta Pérez, 1895 was incorrectly designated by Warncke; the taxon differs from A. obsoleta sensu Warncke, belonging instead to a taxon within the A. mariana Warncke, 1968 complex. A new lectotype is designated for A. obsoleta sp. resurr. from Algeria, and A. mariana solda Warncke, 1974 syn. nov. is synonymised with it; A. (Micrandrena) alma Warncke, 1975 stat. nov. , A. (Micrandrena) mica Warncke, 1974 stat. nov. , and A. (Micrandrena) tenostra Warncke, 1975 stat. nov. are raised to species status. Andrena (Truncandrena) abunda Warncke, 1974 stat. nov. , A. (Micrandrena) lecana Warncke, 1975 stat. nov. , A. (Pruinosandrena) parata Warncke, 1967 stat. nov. , A. (Micrandrena) pauxilla Stöckhert, 1935 sp. resurr. , A. (Pruinosandrena) succinea Dours, 1872 sp. resurr. , and A. (Notandrena) varuga Warncke, 1975 stat. nov. are also returned or elevated to species status. A lectotype is designated for A. (Euandrena) lavandulae Pérez, 1902 sp. resurr. which is returned to species status, and A. (Euandrena) impressa Warncke, 1967 syn. nov. is synonymised with it. Andrena (Truncandrena) nigropilosa Warncke, 1967 stat. nov. is elevated to species status, and A. (Truncandrena) truncatilabris espanola Warncke, 1967 syn. nov. is synonymised with it as a junior subjective synonym. A lectotype is designated for A. (Melandrena) vachali Pérez, 1895; A. (Melandrena) creberrima Pérez, 1895 syn. nov. and A. (Melandrena) vachali syn. nov. are synonymised with A. (Melandrena) discors Erichson, 1841, and Andrena (Melandrena) hispania Warncke, 1967 syn. nov. is synonymised with A. (Melandrena) morio Brullé, 1832. Andrena (Pruinosandrena) mayeti Pérez, 1895 syn. nov. is newly synonymised with A. (Pruinosandrena) caroli Pérez, 1895 and A. (incertae sedis) setosa Pérez, 1903 syn. nov. is newly synonymised with A. (incertae sedis) ranunculorum Morawitz, 1877. Andrena (Simandrena) cilissaeformis Pérez, 1895 sp. resurr. is returned to species status, and is the correct name for A. (Simandrena) breviscopa auctorum. Andrena (incertae sedis) breviscopa Pérez, 1895 is returned to synonymy with A. (incertae sedis) numida Lepeletier, 1841, and A. (incertae sedis) inconspicua Morawitz, 1871 is newly synonymised syn. nov. with A. numida . Andrena (Euandrena) isolata sp. nov. and A. (Micrandrena) ortizi sp. nov. are described from the Sierra Nevada (Granada), A. (Truncandrena) ghisbaini sp. nov. is described from Málaga province, and A. (Avandrena) juliae sp. nov. is described from Cádiz province. The males of A. (Micrandrena) alma and A. (? Euandrena ) ramosa Wood, 2022 are described. Additional lectotypes are designated for A. (Plastandrena) asperrima Pérez, 1895, A. (Plastandrena) atricapilla Pérez, 1895, A. (Aenandrena) hystrix Schmiedeknecht, 1883, A. (Pruinosandrena) lanuginosa Spinola, 1843, A. (Notandrena) ranunculi Schmiedeknecht, 1883, and A. (Euandrena) symphyti Schmiedeknecht, 1883. Neotypes are designated for A. (Chlorandrena) boyerella Dours, 1872, A. (Notandrena) griseobalteata Dours, 1872, A. (Taeniandrena) poupillieri Dours, 1872, A. (Pruinosandrena) succinea Dours, 1872, and A. (incertae sedis) numida Lepeletier, 1841. Type photographs and diagnostic characters are presented in each case, as well as new dietary information for understudied species. Finally, an identification key is presented in order to facilitate future research on this hyper-diverse genus in one of their global diversity hotspots, and current and future research perspectives for Iberian Andrena are discussed.
All three hitherto described species of the Palearctic subgenus Andrena (Longandrena Osytshnjuk, 1993), are revised
and redescribed. This subgenus is characterized by an unusually long glossa, a rare character among short-tongued bees.
A revised diagnosis of this subgenus is given. A key to the species of A. (Longandrena) is provided, and all diagnostic
morphological features are illustrated in detail. The Central Asian species Andrena longiceps Morawitz 1895 is recorded
for the first time from Iran. The distribution map of the subgenus is also presented.
