Lower Cretaceous dinoflagellate cysts of Exmouth Plateau, Nortwest Australia

Cores from Leg 122, Sites 762 and 763, were sampled at intervals of one sample per 1.5-m section in the Lower Cretaceous sequences. More than 400 samples were studied, most of which contained dinoflagellate cysts, spores, pollen, and various types of palynoclasts. From the entire palynomorph assemblage mainly dinoflagellate cysts were studied to give a stratigraphic outline for the Lower Cretaceous. Stratigraphic units were interpreted in terms of zones in use for the Jurassic and Cretaceous of Australia. At both sites a condensed Valanginian to Aptian sequence and an expanded middle to late Berriasian sequence containing a rich microplankton assemblage were recovered. Sites 762 and 763 can be correlated with each other and with the wells Eendracht-1 and Vinck-1.

Neogene planktonic foraminifers from Wombat and Exmouth Plateau

Diverse, warm-water planktonic foraminiferal faunas prevailed on the Wombat and Exmouth plateaus during the Neogene, in spite of the northward drift of Australia across 10° to 15° latitude since the early Miocene. Invasions of cool-water species occurred during periods of global cooling in the late middle Miocene, late Miocene, and Pleistocene, and reflect periods of increased northward transport of cool surface water, probably via the West Australian Current. The sedimentary record of the Neogene on Wombat and Exmouth Plateau is interrupted by two hiatuses (lower Miocene, Zone N5, and upper middle to upper Miocene, Zones N15-N17), and one redeposited section of upper Miocene to uppermost Pliocene sediments. Mechanical erosion or nondeposition by increased deep-water flow or tilting and uplift of Wombat and Exmouth plateaus, resulting in sediment shedding, are the most likely explanations for these Miocene hiatuses, but which of these processes were actually operative on the Wombat and Exmouth plateaus is uncertain. The redeposited section of upper Miocene to uppermost Pliocene sediments in Hole 761B, however, certainly reflects a latest Pliocene period of uplift and tilting of the Wombat Plateau. An important finding was the occurrence of Zone N15-correlative sediments in Hole 762B without any representative of Neogloboquadrina. Similar findings in Java and Jamaica indicate that the earliest spreading of Neogloboquadrina acostaensis in the tropical region resulted from migration. The evolution of this species, therefore, must have taken place in higher latitudes. I suggest that Neogloboquadrina acostaensis evolved from Neogloboquadrina atlantica in the North Atlantic within Zone NN9, but how and where in the region this speciation took place is still uncertain