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Die Grabwespen (Sphecidae sensu Bohart & Menke 1976; Sphecidae sensu lato in neueren, phylogenetischen Arbeiten), zu denen nach Day (1984) und späteren Autoren auch die Heterogynaidae zählen, umfassen derzeit 266 Gattungen mit 9559 beschriebene Arten (Pulawski 2006). Zusammen mit den Bienen (= Apiformes nach Michener 2000, bzw. Anthophila nach Engel 2005) bilden die Grabwespen ein gut begründetes Monophylum, das nach Michener (1986) den Namen Apoidea trägt und eine der drei Hauptlinien innerhalb der aculeaten Hymenoptera ist. Die Monophylie der aculeaten Hymenoptera, der Apoidea sowie die der Bienen ist jeweils gut begründet (z.B. Brothers 1975, Königsmann 1978, Lomholdt 1982, Alexander 1992, Brothers & Carpenter 1993). Anders verhält es sich mit den Grabwespen. Neben der phylogenetischen Untersuchung von Brothers & (1993), die die Monophylie der Grabwespen unterstützt, haben andere morphologische als auch molekularsystematische Analysen starken Zweifel an dieser Hypothese aufkommen lassen (z.B. Königsmann 1978, Lomholdt 1982, Alexander 1992, Prentice 1998, Melo 1999, Ohl & Bleidorn 2006).
The Afrotropical species of the sphecid genus Sphex are revised. Forty-six taxa are recognized, of which fifteen are newly described: Sphex abbotti nivarius subsp. nov., S. comorensis sp. nov., S. hades sp. nov., S. nefrens sp. nov., S. occidentalis sp. nov., S. pseudopraedator sp. nov., S. pseudosatanas sp. nov., S. pulawskii sp. nov., S. rufoclypeatus sp. nov., S. satanas memnon subsp. nov., S. schmideggeri sp. nov., S. schoutedeni malawicus subsp. nov., S. socotrensis sp. nov., S. stadelmanni rufus subsp. nov. and S. victoria sp. nov. A new subgenus, Menkeella subgen. nov., is proposed for S. paulinierii Guérin Méneville, 1843.
Four former synonyms are resurrected: Sphex pruinosus var. haemorrhoidalis Magretti, 1898, for which the replacement name of S. feijeni nom. nov. is proposed, S. camerunicus Strand, 1916, S. cinerascens Dahlbom, 1843 and S. abbotti W. Fox, 1891.
Nine of the previously valid names are shown to be junior synonyms: Sphex haemorrhoidalis basuto (Arnold, 1947) and S. haemorrhoidalis kobrowi (Arnold, 1928) = S. umtalicus Strand, 1916; S. incomptus anonymus Leclercq, 1955 = S. nigrohirtus Kohl, 1895; S. neavei (Arnold, 1928) = S. abbotti W. Fox, 1891; S. observabilis (R. Turner, 1918) = S. ahasverus Kohl, 1890; S. rufiscutis (R. Turner, 1918) and S. mochii Giordani Soika, 1942 = S. jansei Cameron, 1910; S. rufiscutis laevigatus Arnold, 1951 = S. gaullei Berland, 1927; and S. stadelmanni integer (Arnold, 1928) = S. stadelmanni Kohl, 1895. Three previously synonymized species are transferred as new synonyms to different species: Sphex conradti Berland, 1927 = S. camerunicus Strand, 1916; S. kilimandjaroensis Cameron, 1908 = S. abbotti W. Fox, 1891; and S. nigripes var. pachyderma Strand, 1916 = S. umtalicus Strand, 1916. For three species, the actual type localities are on different continents than their labels indicate: Sphex ahasverus Kohl, 1890, S. castaneipes Dahlbom, 1843 and S. optimus F. Smith, 1856, with the first occuring in Africa instead of Australia and the other two presumably occuring in South America instead of Africa.
The occurrence of the argentatus group in Sub-Saharan Africa is confirmed, and seven additional species groups are established, with all but one of them based on apomorphic morphological traits. A hypothesis on the phylogenetic relationships among the subgenera and species groups of Sphex is presented, and an identification key for both sexes as well as a placoid-based identification table for males are presented. Using Bayesian inference and maximum likelihood analysis on mitochondrial and nuclear sequence data generated from thirty-one of the recognized taxa, the monophyly of the proposed species groups is corroborated.