Gap. Gibson et al., Phylogenetics and classification of Chalcidoidea and Mymarommatoidea - a review of current concepts (Hymenoptera, Apocrita), ZOOL SCR, 28(1-2), 1999, pp. 87-124
Classification and morphological and molecular evidence supporting relation
ships of Mymarommatidae (Mymarommatoidea) and the 20 families of Chalcidoid
ea are reviewed. Five autapomorphies support monophyly of Mymarommatoidea,
at least two autapomorphies support monophyly of Chalcidoidea, and three sy
napomorphies support a sister-group relationship between Mymarommatoidea an
d Chalcidoidea. Mymaridae are indicated as the likely sister group of all o
ther Chalcidoidea by: two features of the ovipositor, the unique structure
of a muscle between the mesofurca and axillary lever, and sequence data fro
m the 28s rDNA gene. Structure of the upper valvulae of the ovipositor coul
d indicate Rotoitidae as the second-most basal clade of Chalcidoidea. Chalc
ididae, Elasmidae, Encyrtidae, Eulophidae, Eurytomidae, Leucospidae, Mymari
dae, Ormyridae, Rotoitidae, Signiphoridae, Torymidae and Trichogrammatidae
are each indicated as monophyletic by at least one putative synapomorphy, b
ut could render other families paraphyletic. Aphelinidae, Eupelmidae, Ptero
malidae, and Tetracampidae are not demonstrably monophyletic. Agaonidae is
monophyletic only if restricted to Agaoninae, and Eucharitidae is monophyle
tic only if restricted to Eucharitinae + Oraseminae. Eupelmidae may be para
phyletic with respect to Tanaostigmatidae and Encyrtidae, and Tanaostigmati
dae including Cynipencyrtus may be paraphyletic relative to Encyrtidae. Per
ilampidae (Perilampinae + Chrysolampinae) are either polyphyletic or paraph
yletic with respect to Eucharitidae + Akapalinae + Philomidinae. No cladist
ic hypotheses of familial relationships based on character evidence have co
nsidered the superfamily in its entirety.