The Late Ordovician–Early Silurian succession in Jämtland includes the marine Kogsta Siltstone, which is unconformably overlain by the shallow-water Ede Quartzite that grades into the open-marine Berge Limestone. A Hirnantia shelly fauna dates the uppermost Kogsta Siltstone as Hirnantian, and shelly fossils indicate an Aeronian age for the Berge Limestone. Biostratigraphically highly diagnostic conodonts of the early-middle Aeronian Pranognathus tenuis Zone provide the first firm date of the Upper Ede Quartzite and the lowermost Berge Limestone. The Lower Ede Quartzite has not yielded fossils, but sedimentological data suggest it to be of Hirnantian age and reflect the glacio-eustatic low-stand. The contact between the Lower and Upper Ede Quartzite, here taken to be the Ordovician–Silurian boundary, appears to be an unconformity associated with a stratigraphic gap that at least includes the Rhuddanian Stage. The biostratigraphically important conodonts Pranognathus tenuis, Kockelella? manitoulinensis, and Pranognathus siluricus are recorded from Sweden for the first time, and these and other conodonts are used for correlations with coeval units in Europe and North America. In a regional review of Aeronian conodont faunas, three intergrading, apparently depth-related, conodont biofacies are recognised, the Jämtland conodonts representing the one characteristic of the shallowest water.

The protaspid ontogeny of Bolaspidella housensis (Walcott, 1886) is re-described. This species is known from the Marjum Formation (Lower Marjuman Stage) of western Utah, USA. Three protaspid stages are recognised, with the instars discriminated most readily by different spacing between the postero-lateral ends of the fixigena. Protaspides of B. housensis are shown to be similar to those of Glaphyraspis parva, from several Upper Cambrian localities in the USA, and Ptychopariide sp. E from the Upper Cambrian of the Wasatch Mountains in Utah, USA.

Redescription of the cranial anatomy of Ariekanerpeton sigalovi (Seymouriamorpha: Discosauriscidae; Lower Permian, Tadzhikistan) highlights new diagnostic features which permit a new skull reconstruction and revised diagnosis. The largest Ariekanerpeton specimens differ from like-sized Discosauriscus, a second member of Discosauriscidae, in showing: oblique anterior margin of tabular ornamented surface; acute, elongate posterolateral corner of supratemporal; postorbital ventrolateral ramus with small anteroventral process and forming oblique suture with jugal dorsomedial ramus; jugal posterior ramus tapering rearward, forming subhorizontal suture with quadratojugal; weak ventral sculpture lateral to pterygoid articular recess; parasphenoid subrhomboidal, with lightly sculptured anterior wedge-like process; more densely arranged denticle rows on top of low radiating ridges on pterygoid palatal ramus. Gill filaments occur in specimens with skull lengths of up to 30 mm. Detailed examination of ontogenetic changes in Ariekanerpeton and comparisons with other seymouriamorphs are presented.

The postcranial skeleton of Ariekanerpeton sigalovi (Seymouriamorpha: Discosauriscidae; Lower Permian, Tadzhikistan) differs from that of like-sized Discosauriscus specimens in showing: wider interclavicle anterior plate with smaller, rhomboidal sculptured field on its ventral surface not reaching plate posteromedial margins; broader interclavicle plate-stem junction; slightly narrower interclavicle posterior stem; anteroposteriorly narrower clavicle ventral plate with convex posterior margin; shorter, more robust humerus; four phalanges on fourth manus digit (five phalanges in Discosauriscus); ilium more elongate dorsoventrally with anteroposteriorly narrower neck; posterior process of iliac blade oriented distinctly posterodorsally rather than horizontally; more gracile atlantal rib; broadened distal end of second presacral rib. A revised cladistic analysis of the best known seymouriamorph species retrieves Ariekanerpeton either as sister group to both species of Discosauriscus, or to D. austriacus only.