Abstract Nine non-pollen palynomorph (NPP) groups occur in Quaternary marine and brackish-water sediments; these groups represent various planktonic or micro- to macrobenthic organisms. Some extant NPP were previously classified as fossil Acritarcha, Chitinozoa or scolecodonts. We refer to reviews of these fossils and their applications for Paleozoic–Mesozoic biostratigraphy and palaeoecology but focus on extant marine NPP that can be studied by laboratory culture, genetics or micro-geochemical methods. Marine NPP include resting cysts of planktonic dinoflagellates and prasinophytes, tintinnids and other cilates, copepod eggs and skeletal remains, and various microzoobenthos: microforaminiferal organic linings, ostracod mandibles and carapace linings, various worm egg capsules and mouthparts. New micro-Fourier Transform Infrared spectroscopy spectra suggest the probable affinities of the tintinnid cyst type P and Beringiella . Our applications in marine biodiversity and provincialism studies emphasize under-studied polar regions and neglected ice-algae nano-plankton and compare climate-based NPP distributions to Ocean Biogeographic Information System realms. Trophic relationships are outlined using sediment-trap studies. Seasonal to annual-scale investigations of palaeoproduction provide new perspectives on ocean carbon budgets during times of rapid climate change and atmospheric carbon increase. More taxonomic and source-linkage studies of non-dinocyst marine NPP are needed but we outline potentials for studies of hemispheric or global-scale shifts in marine food webs as driven by ocean warming.

Abstract: Understanding the ecological roles of pterosaurs is a challenging pursuit, but one aided by a growing body of fossil evidence for their dietary preferences and roles as food sources for other species. Pterosaur foraging behaviour is represented by preserved gut content, stomach regurgitates, coprolites and feeding traces. Pterosaurs being eaten by other species are recorded by tooth marks and teeth embedded in their fossil bones, consumer gut content and regurgitate, and their preservation entangled with predatory animals. This palaeoecological record has improved in recent years, but remains highly selective. The Jurassic rhamphorhynchid Rhamphorhynchus , Cretaceous ornithocheiroid Pteranodon and azhdarchid pterosaurs currently have the most substantial palaeoecological records. The food species and consumers of these taxa conform to lifestyle predictions for these groups. Rhamphorhynchus and Pteranodon ate and were eaten by aquatic species, matching expectations of these animals as sea-going, perhaps partly aquatic species. Possible azhdarchid pterosaur foraging traces alongside pterosaur tracks, and evidence that these animals were eaten by dinosaurs and Crocodyliformes, are consistent with hypotheses that azhdarchids foraged and lived in terrestrial settings. Fossil evidence of pterosaur palaeoecology remains rare: researchers are strongly encouraged to put specimens showing details of dietary preferences, foraging strategies or interactions with other animals on record.

Abstract A siliceous permineralized peat block recovered from Hopen in the Svalbard archipelago hosts a low-diversity Late Triassic flora dominated by autochthonous roots and stems of bennettitaleans and lycophytes, and parautochthonous leaves, sporangia, spores and pollen from a small range of pteridophytes and gymnosperms. Some parenchymatous bennettitalean root cells show interactions with chytrid fungi and bacteria; the remains of other fungi and fungi-like organisms are dispersed within the peat’s detrital matrix. Cavities excavated through some roots and compacted detritus contain abundant coprolites probably derived from sapro-xylophagous oribatid mites, although no body fossils have yet been identified. Sparse larger coprolites containing leaf fragments attest to the presence of invertebrate folivores in the ancient ecosystem. The low-diversity flora, relatively few trophic levels and simple nutritional web, together with sedimentological aspects of the host formation and the peat structure, collectively favour accumulation of the organic mass as a fibric (root-dominated) peat within a temperate (high middle-latitude), well-aerated mire.