The New World species of Loxocera Meigen are revised including two new species, L. (Imantimyia) ignyodactyla Buck sp. n. from Costa Rica (first record of the genus from the Neotropical region) and L. (Imantimyia) ojibwayensis Buck sp. n. from Ontario, Canada. Loxocera californica Capelle is synonymized with L. collaris Loew and lectotypes are designated for L. pleuritica Loew and L. cylindrica var. obsoleta Johnson (both synonyms of L. cylindrica Say). The New World species are diagnosed and a key to species is provided. The male and female terminalia of Loxocera are described in detail for the first time, and their functional morphology is discussed. Eggs of most species are described and a key to the known eggs of Loxocera is provided. A phylogenetic framework for the Holarctic subgenera and species groups of Loxocera is developed based on morphological characters of the adult flies. The Old World subgenus Platystyla Macquart is synonymized with Loxocera s. str., and Imantimyia Frey is reinstated as a valid subgenus including all Holarctic species previously placed in Loxocera s. str. except the L. aristata species group. This leads to the following new subgeneric combinations: L. (L.) malaisei Frey comb. n., L. (L.) matsumurai Iwasa comb. n., L. (L.) monstrata Iwasa, comb. n., and L. (L.) omei Shatalkin comb. n. The species groups of Imantimyia are redefined, i.e. the L. achaeta-group (7 spp.), the L. fulviventris-group (4 spp.), and the L. albiseta-group (1 sp.). The Oriental subgenus Asiopsila Shatalkin is referred to Psila Meigen s. l. as a subgenus based on characters of the egg, resulting in fourteen new generic combinations: Psila (Asiopsila) brevibuccata (Shatalkin) comb. n., P. (A.) burmanica (Frey) comb. n., P. (A.) decorata (de Meijere) comb. n., P. (A.) derivata (Shatalkin) comb. n., P. (A.) formosana (Hennig) comb. n., P. (A.) freidbergi (Shatalkin) comb. n., P. (A.) humeralis (de Meijere) comb. n., P. (A.) kambaitensis (Frey) comb. n., P. (A.) limpida (Shatalkin) comb. n., P. (A.) maculipennis (Hendel) comb. n., P. (A.) michelseni (Shatalkin) comb. n., P. (A.) pleuralis (Frey) comb. n., P. (A.) primigena (Shatalkin) comb. n., and P. (A.) vittipleura (Shatalkin) comb. n.
The type species of Pseudopsila Johnson, P. fallax (Loew), and two related species are found to belong in Psila s. str., and Pseudopsila is thus synonymized with Psila Meigen. The remaining species formerly included in Pseudopsila form a monophyletic group here described as Xenopsila Buck subgen. n. [i.e., Psila (Xenopsila) collaris Loew comb. n., P. (X.) bivittata Loew comb. n., P. (X.) lateralis Loew comb. n., P. (X.) arbustorum Shatalkin comb. n., P. (X.) nemoralis Shatalkin comb. n., P. (X.) tetrachaeta (Shatalkin) comb. n., P. (X.) maculipennis (Frey) comb. n., P. (X.) nigricollis (Frey) comb. n., P. (X.) nigrohumera (Wang & Yang) comb. n.]. A key to the Nearctic species of Xenopsila and the Psila fallax-group is provided. The placement of Xenopsila in Psila s. l. is confirmed by newly recognised synapomorphies of the egg stage. The somewhat questionable monophyly of Psila s. l. is confirmed based on these new synapomorphies, thereby slightly expanding its taxonomic limits to also include Asiopsila Shatalkin. The morphology of the male genitalia of Xenopsila is discussed in detail, clarifying confused homologies and character polarities in the hypandrial complex. Evolutionary trends in the development of the hypandrium in the subfamily Psilinae are discussed.