The identity of the type-species of Gonatocerus Nees (Hymenoptera: Mymaridae)

The validity of Gonatocerus Nees is discussed, and the identity of the type-species, G.longicornis, is established. Generic and specific synonymy is listed, and the neotype female of G.longicornis is redescribed.     

Rotoitidae, a curious new family of Chalcidoidea (Hymenoptera) from New Zealand

Abstract. A new chalcidoid family, Rotoitidae fam.n., is described from New Zealand. The probable systematic affinities of Rotoitidae are discussed and the type genus and a single included species, Rotoita basalis gen. et sp.n., are described and illustrated.     

Asymmetry in an Ordovician conulariid cnidarian

Sendino, C., Zágor?ek, K. & Taylor, P.D. 2012: Asymmetry in an Ordovician conulariid cnidarian. Lethaia, Vol. 45, pp. 423–431. Conulariids are fossils of the presumed polyps of an extinct scyphozoan cnidarian group. Their cone‐shaped skeletons normally show perfect tetraradial symmetry. However, in the Ordovician species Metaconularia anomala ( Barrande 1867 ) from Drabov (Czech Republic), tetraradial symmetry is compromised in three ways: (1) the skeleton often shows torsion; (2) the four sides may vary in width at the same level within one individual; and (3) one side may be deleted to give a triradial skeleton. Almost 2000 specimens were studied in museum collections. About 56% of analysed specimens are twisted in an anticlockwise direction (sinistral) when viewed from the apex towards the aperture, 28% show no torsion, 1% exhibit clockwise torsion (dextral) and the remaining 15% cannot be classified. Maximum measured torsion rate was 1.5°/mm. A significant negative correlation between torsion rate and length suggests that more highly torted individuals may have survived less well. Almost 5% of individuals show loss of one side for at least part of their lengths. Although many individuals have four sides of equal width, in a significant proportion the sides are of unequal width, up to a maximum/minimum side width ratio of 2 (i.e. widest face twice the width of the narrowest). In the absence of a satisfactory taphonomic model to explain the asymmetries, they are regarded as mirroring asymmetries in the living conulariids, with the strong preference for sinistral torsion interpreted as an example of a fixed asymmetry that was genetically controlled and heritable. It is speculated that the signalling protein Nodal as well as Hox‐like genes were involved in controlling the asymmetries described in M. anomala.