The olistostromes form two belts within the Pieniny Klippen Belt (PKB) in the Northern Carpathians. They mark an early stage of the development of the accretionary prism. The first belt was formed during Late Cretaceous time as a result of subduction of the southern part of the Alpine Tethys. The fore-arc basin originated along this subduction zone, with synorogenic flysch deposits. Huge olistoliths deposited within the Cretaceous–Palaeogene flysch of the Złatne Basin, presently located in the vicinity of the Haligovce village (eastern Slovakia), provide a good example of the fore-arc olistostrome setting. The second belt is related to the movement of the accretionary prism, which overrode the Czorsztyn Ridge during Late Cretaceous–Paleocene time. The destruction of this ridge led to the formation of submarine slumps and olistoliths along the southern margin of the Magura Basin. The Upper Cretaceous – Paleocene flysch sequences of the Magura Basin constitute the matrix of olistostromes. The large Homole block in the Jaworki village represents the best example of the Magura Basin olistolith. Numerous examples of olistoliths were documented in western Slovakia, Poland, eastern Slovakia and Ukraine. The olistostromes formed within the Złatne and Magura basins orginated during the tectonic process, forming the olistostrome belts along the strike of the PKB structure.

The stratigraphy, palaeoecology and palaeobiogeography are outlined for two genera and ten species of Jurassic planktonic foraminifera described in Gradstein et al. (Swiss J Palaeontol 2017 . doi: 10.1007/s13358-017-0131-z ). The two genera are Globuligerina and Conoglobigerina. Globuligerina probably appeared in late Toarcian (late Early Jurassic) and Conoglobigerina first occurred in Middle Oxfordian (early Late Jurassic). Within the two genera ten species are defined, including from older to younger: Globuligerina dagestanica (Morozova), G. avariformis (Kasimova), G. balakhmatovae (Morozova), G. oxfordiana (Grigelis), G. bathoniana (Pazdrowa), G. jurassica (Hofman), G. oxfordiana (Grigelis) calloviensis Kuznetsova emended, G. tojeiraensis Gradstein, Conoglobigerina helvetojurassica (Haeusler), C. grigelisi Gradstein and C. gulekhensis (Gorbachik and Poroshina). Globuligerina balakhmatovae, G. oxfordiana and G. bathoniana are longer ranging, although there are subtle evolutionary trends in these taxa that may refine stratigraphic usage. Other taxa have shorter stratigraphic ranges. Using stratigraphic trends, test morphology and wall texture changes, the species are tentatively assembled in four evolutionary groups, termed A–D, and in six zones from Late Toarcian through Tithonian. The greater species diversity and possibly also specimen abundance took place in the Kimmeridgian, a time of high global sea level and greenhouse palaeoclimatic conditions. Jurassic planktonic foraminifera preferred marine continental margin conditions instead of the distal open ocean and spread from offshore Eastern Canada to offshore Western Australia along the margins of the Tethys Ocean. The group did not venture into austral or boreal realms, likely reasons why migration probably failed to the west coasts of South and North America.

The taxonomy is modernized and updated for Jurassic planktonic foraminifera using all available literature and stratigraphic series of sediment samples from Canada, Portugal, France, Switzerland, Poland, Lithuania, Russia and Dagestan. The regional stratigraphy of all sampled sections is outlined. Many of the 65–200 µm sample residues yielded well-preserved free specimens, with local assemblages containing up to six species. Thin sections were studied also but do not allow detailed taxonomy. Two genera are described: Globuligerina and Conoglobigerina. Globuligerina probably appeared in the late Toarcian (late Early Jurassic) and Conoglobigerina first occurred in middle Oxfordian (early Late Jurassic). A principal difference between Globuligerina and Conoglobigerina is that the former has a smooth to pustulose wall surface texture and the latter a reticulate wall surface texture. Within the two genera, ten species are described, including from older to younger: Globuligerina dagestanica (Morozova), G. avariformis (Kasimova), G. balakhmatovae (Morozova), G. oxfordiana (Grigelis), G. bathoniana (Pazdrowa), G. jurassica (Hofman), G. oxfordiana (Grigelis) calloviensis Kuznetsova emended, G. tojeiraensis Gradstein, Conoglobigerina helvetojurassica (Haeusler), C. grigelisi Gradstein and C. gulekhensis (Gorbachik and Poroshina). The coarsely perforate ‘Globuligerina’ stellapolaris needs more investigation to establish its identity as a Jurassic or a Late Cenozoic taxon (Gradstein 2017a ). Globuligerina balakhmatovae, G. oxfordiana and G. bathoniana occur from Bajocian through early Kimmeridgian, or even Tithonian. Subtle morphological trends may refine stratigraphic usage. Other taxa have shorter stratigraphic ranges. Nineteen plates and ten type species figures detail morphology of all taxa. For key taxa, both the types and specimens from other localities are illustrated.