Abstract
Principal attention is focused on phytostratigraphy and comparative palaeofloristics of the Anadyr-Koryak (AKSR) and Northern Alaska (NASR) subregions of the North Pacific Region. The high-resolution Upper Albian-Paleocene phytostratigraphic schemes of these subregions are based on perceived stages of their floral evolution. In the AKSR the scheme includes seven subdivisions of subregional extent: the Early Ginter (upper Albian), Grebenka (upper Albian-Cenomanian-lower Turonian), Penzhina (upper Turonian), Kaivayam (Coniacian), Barykov (Santonian-lower to ?middle Campanian), Gornorechenian (?upper Campanian-lower Maastrichtian), and Koryak (lower to upper Maastrichtian-?Danian) phytostratigraphic horizons. The phytostratigraphic scheme of the NASR includes three subregional phytostratigraphic horizons and five plant-bearing beds. These are the Kukpowruk (?lower to middle-?upper Albian), Niakogon (upper Albian-Cenomanian), Kaolak (Turonian) horizons and beds with the Tuluvak (Coniacian), Early Kogosukruk (upper Santonian-Campanian), Late Kogosukruk (Campanian-Maastrichtian), Early Sagwon (Danian-Selandian), and Late Sagwon (Selandian-Thanetian) floras. The comparative analysis of coeval (or close in age) floras distinguished in the AKSR and NASR shows that they are either similar to each other (floras Early Ginter and Kukpowruk, Grebenka and Niakogon, Penzhina and Kaolak, Koryak and Early Sagwon) or different in systematic composition (floras Kaivayam and Tuluvak, Gornorechenian and Kogosukruk). Similarities between the floras imply that plant assemblages of two subregions evolved under comparable climatic conditions and freely intercommunicated via the Bering Land Bridge during the Albian-Turonian and terminal Maastrichtian-Paleocene. Floras of the AKSR and NASR, which are of different composition, existed in particular intervals of geological history when trans-Beringian plant migrations were limited or even ceased because of palaeoclimatic difference between the subregions. Floras of the AKSR and NASR survived crisis at the Cretaceous-Paleogene boundary without essential evolutionary consequence which does not support a hypothesis of a global ecological crisis at this boundary. From the analysis of the Arctic end-Cretaceous flora and palaeoclimate we conclude that the large Northern Alaskan dinosaurs were driven by lack of resources (food and shelter) to migrate 1200–1300 kilometres to the South to find forage, warmer temperatures and better light conditions before winter set in. A scenario of the Albian-Late Cretaceous florogenesis in the North Pacific Region is proposed. A primary driver of Albian-Late Cretaceous florogenesis was the gradual invasion by novel angiosperm-rich plant communities into the Asiatic continental interiors and a replacement of pre-existing vegetation dominated by ancient ferns and gymnosperms. Plant fossils representing Mesophytic and Cenophytic communities usually do not mix in the individual assemblages.
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Herman, A.B. Albian-Paleocene flora of the north pacific: Systematic composition, palaeofloristics and phytostratigraphy. Stratigr. Geol. Correl. 21, 689–747 (2013). https://doi.org/10.1134/S0869593813070034
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DOI: https://doi.org/10.1134/S0869593813070034