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A new ant genus from the late Eocene European amber

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Eocenomyrma gen. nov. of extinct ants of the family Formicidae, subfamily Myrmicinae, is described from the late Eocene European amber (ca. 40 Ma), based on six specimens from six pieces of amber; three of them contain E. rugosostriata (Baltic and Saxonian ambers); the remainder contain three new species: E. orthospina (Baltic Amber), E. electrina (Scandinavian Amber), and E. elegantula (Baltic Amber). Eocenomyrma resembles two extant genera: Myrmica and Temnothorax (both of which also occur in late Eocene European amber), but differs from them by the following apomorphies: clypeus short and broad, with two lateral longitudinal carinae and distinctly marked anterolateral corners, its median portion faintly concave transversally, anterior margin broad and shallowly concave medially, with pairs of long setae situated on the anterolateral clypeal corners, and central part of the anterior clypeal margin without setae; middle and hind tibiae lacking the spurs. Palp formula in Eocenomyrma is 4, 3 versus 6, 4 in Myrmica. We include Eocenomyrma in the tribe Formicoxenini. Nothomyrmica rugosostriata is transferred to Eocenomyrma, and the neotype of the latter species is designated; Nothomyrmica petiolata is transferred to the genus Temnothorax. A key for the identification of all known Eocenomyrma species is compiled.
Usomyrma mirabilis gen. et sp. nov., belonging to the tribe Leptomyrmecini of the subfamily Dolichoderinae, are described based on two males from the late Eocene Danish Amber. Usomyrma differs from Leptomyrmex by a set of plesiomorphic and autapomorphic features. Distinctly plesiomorphic characters include the fore wing venation, i.e., the presence of the well developed pterostigma, the wide closed cell 3r and the big central closed cell that formed by the fusion of the cells (1+2r)+mcu, and the structure of mandibles, which are elongate-triangular, with a well developed masticatory margin that, unlike Leptomyrmex, possesses a set of well developed, relatively long and sharp teeth. The most distinctive autapomorphy of Usomyrma is the structure of the antennae: although it remains 13-segmented, its second funicular segment is extremely elongate, much longer than any other segment, including the apical one. The generic composition of the tribe Leptomyrmecini is partly reassessed compared to the previously published data. We propose to establish a new informal Leptomyrmex genus-group within tribe Leptomyrmecini, including in it the extant genus Leptomyrmex, two fossil (Usomyrma gen. nov., Leptomyrmula) and a “Leptomyrmex” male from the Dominican Amber that probably represents a third extinct genus. Finally, a new, alternative evolutionary and zoogeographic scenario for the Leptomyrmex genus-group is proposed. We suggest that fore wing venation of Usomyrma is ancestral to other genera of this group. The next evolutionary step was the complete reduction of the closed central cell in Leptomyrmula, while conserving the pterostigma and a wide closed cell 3r. Then, in the modern Leptomyrmex males the pterostigma was reduced and the cell 3r became very narrow. Finally, the most apomorphic condition is illustrated by the venation of “Leptomyrmex” male from the Dominican Amber, which has no pterostigma and pterostigmal appendages, combined with the absence of the closed cell 3r. As a result, we suppose that the ancestor of Leptomyrmex might penetrate from Eurasia to Australia via South-East Asia, and then Leptomyrmex penetrated to South America, where the most advanced morphologically form (i.e., “Leptomyrmex” male from the Dominican Amber) arose, but extinct in Miocene.
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