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Pseudoplankton

All attached epifaunal species have the potential to colonize floating substrates such as driftwood, externally shelled cephalopods, Sargassum-like algae and marine vertebrates. Such pseudoplankton are preserved in a much wider range of facies than their benthic relatives. However, they are never as abundant as benthos due to the rarity of attachment sites. Pseudoplanktonic species utilize five attachment strategies: cemented, adpressed, pendent, boring and clinging.

Cenomanian micromorphic ammonites from the Western Interior of the USA

Calcareous concretions from middle and upper Cenomanian (Cretaceous) shale sequences in Montana and Wyoming yield, on rare occasions, abundant minute ammonites. Some are juveniles of large species, and give valuable evidence on early ontogeny and evolutionary affinities of these taxa. They provide evidence for the probable evolutionary origins of a series of hitherto undescribed progenic dwarf genera, adult at 4-5-16-5 mm diameter that are a remarkable feature of these assemblages.

Early Mississippian Hyolitha from northern Iowa

The exceptionally fine preservation and large number of specimens from a single late Palaeozoic locality makes the hyoliths in the Humboldt Oolite (Osagean, lower Mississippian) unique. All specimens are assigned to Gerkella humboldti n. gen., n. sp., family Hyolithidae, order Hyolithida. There is considerable variation in certain morphological features, such as transverse shape, nature of ornament and apical curvature; however, these differences are judged to be gradational.

A discoglossid frog from the Middle Jurassic of England

A discoglossid frog, Eodiscoglossus oxoniensis sp. nov. is described from the Upper Bathonian Forest Marble of Oxfordshire. It closely resembles Eodiscoglossus santonjae from the Jurassic-Cretaceous boundary of Spain but can be distinguished by characteristics of the ilium and premaxillary. The E. oxoniensis specimens represent the earliest European material critically identifiable as a frog and the earliest discoglossid yet recognised.

Late Cainozoic brachiopods from the coast of Namaqualand, South Africa

An unusual late Tertiary - early Quaternary brachiopod assemblage from shallow water shoreline deposits on the Namaqualand coastal plain of South Africa is described. New species described are Kraussina, rotundata, K. laevicostata, K. cuneata and Cancellothyris platys, with subspecies C. platys platys and C. platys petalos. In situ specimens, shell growth, abrasion and epizoans all indicate crowded living conditions, commonly on bedrock.

Lower Cretaceous spiders from the Sierra de Montsech, north-east Spain

Four new specimens of spiders (Chelicerata: Araneae), from Lower Cretaceous (Berriasian-Valan-ginian) lithographic limestones of the Sierra de Montsech, Lerida Province, north-east Spain, are described, as Cretaraneus vilaltae gen. et sp. nov., Macryphantes cowdeni gen. et sp. nov. (two specimens), and Palaeouloborus lacasae gen. et sp. nov. All belong to the infraorder Araneomorphae.

Giant acanthomorph acritarchs from the Upper Proterozoic in southern Norway

Large microfossils from a single phosphatic pebble in the late Riphean-early Vendian ( > 612+ 18 — 665+ 10 Ma) Biskopas Conglomerate in the Hedmark Group in southern Norway were described by Spjeldnaes (1963) under the name Papillomembrana compta and interpreted as a possible dasycladacean alga. The microfossils are evidently organic-walled and here regarded as giant acanthomorph acritarchs. The diagnosis of Papillomembrana compta is emended. Possibly related Proterozoic taxa are discussed. A new acanthomorph acritarch, Ericiasphaera spjeldnaesii gen. et sp. nov., found with P.

Orientation of cephalopod shells in illustrations

Most drawings and photographs of fossil cephalopods show the shell upside down in respect to the animal's living position. As there is no advantage in this way of making illustrations, presumably based ot tradition, the author suggests that fossil as well as living cephalopods should be illustrated in life position. This is particularly important today, as functional morphology is of vital interest to cephalopod workers. To facilitate understanding of the behaviour of fossil cephalopods, the first step must be to see them orientated in the same way as they saw each other.
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