Previously, it was believed that there was a dramatic turn-over in the fauna of beavers (Rodentia, Castoridae) from the Barstovian to the Clarendonian from Nebraska. Stratigraphically controlled collections of fossil castorids from the Valentine Formation, which cross this boundary, now indicate that a complete change in the castorid fauna did not occur, but instead a more gradual change and replacement of earlier taxa with more advanced taxa occurred. The range of Eucastor tortus and Monosaulax skinneri is extended from late Barstovian into the latest Barstovian Devil's Gulch Member and the range of the otherwise Clarendonian species of Prodipoides is extended downward into the late Barstovian Crookston Bridge Member. The skulls of Monosaulax skinneri and Eucastor valentinensis are described in detail for the first time. The cranial morphology of M. skinneri is primitive for Castoroidini and that of E. valentinensis is specialized for tooth-digging behavior as in the Nothodipoidini. A new genus, Temperocastor, is proposed for E. valentinensis based on its primitive morphology of the cheek teeth and derived cranial morphology. Temperocastor represents the most primitive nothodipoidine.

An exceptionally preserved skull and mandible of ceratopsian dinosaur Psittacosaurus major revealed many anatomical details such as the existence of an elliptical median interpremaxillary foramen, a prominent neurovascular canal on the internal wall of the beak, long, slightly divergent basipterygoid processes developed as vertical blades with a deep cleft between them, and horizontally oriented vomer. The new specimen shows two autapomorphies of Psittacosaurus major, the transversely narrow dorsal skull roof and very prominent dentary flanges, confirming the presence of two large-skulled psittacosaur species in the Lujiatun Bed of the Lower Cretaceous Yixian Formation in Beipiao City, western Liaoning Province, China, the long- and narrow-skulled P. major, and broad-skulled P. lujiatunensis.

Numerous tracks and trackways are preserved in the a cross-strata of the Lower Jurassic Navajo Sandstone of northern Arizona and southern Utah, USA. Tracks and trackways of small theropod dinosaurs are particularly abundant within one 10-m-thick interval. This paper describes a crouching trace from a theropod dinosaur that shows impressions of all four limbs, the ischial callosity, the tail, and tracks leading to and away from the crouching site, and revises the interpretation of a well preserved trackway hitherto referred to the synapsid ichnogenus Brasilichnium and here considered to be from a sauropodomorph dinosaur. It is named Navahopus coyoteensis isp. nov. on the basis of morphological differences from the type ichnospecies N. falcipollex. The ichnofamily Navahopodidae is revised to include Tetrasauropous unguiferus, Navahopus falcipollex, and N coyoteensis.

A new exquisitely preserved stem group echinoderm (cinctan), Lignanicystis barriosensis gen. et sp. nov., is described from the Middle Cambrian of Los Barrios de Luna, North Spain. This displays a unique asymmetrical body plan with ventral projecting nodes that raised the lower surface above the substratum. There are four openings through the body wall: mouth, anus, atrium, and an aligned row of suturai pores of uncertain function. Unlike other cinctans, Lignanicystis has a strongly asymmetrical shape convergent with that of some cornute carpoids. Like cornutes, the test is also elevated above the substratum to allow water flow beneath the theca. In both cases this is probably an adaptation to life in higher water flow regimes.

Protanastrophia repanda gen. et sp. nov. is a reef-dwelling parastrophinid brachiopod in the Lower Silurian (uppermost Telychian) Attawapiskat Formation of the Hudson Bay region of Canada. It is characterized by a small, quasi-smooth shell with gentle anterior costae, a tendency towards an asymmetrical, sigmoidal anterior commissure, and widely separate, subparallel inner hinge plates. Protanastrophia first appeared in the marginal seas of Siberia (Altai, Mongolia) during the Late Ordovician, retaining the primitive character of discrete inner hinge plates in the superfamily Camerelloidea, and preferred a carbonate mound depositional environment. It survived the Late Ordovician mass extinction and subsequently spread to Baltica and Laurentia during Early Silurian (Llandovery) time. Superficially similar asymmetrical shells of Parastrophina portentosa occur in the Upper Ordovician carbonate mound facies of Kazakhstan but differ internally from the new genus in having a septum-supported septalium. Phylogenetic analysis indicates that, within the Camerelloidea, asymmetrical shells with a sigmoidal anterior commissure evolved in Protanastrophia repanda and Parastrophina portentosa independently during the Late Ordovician as a case of homoplasy. The two species belong to separate parastrophinid lineages that evolved in widely separate palaeogeographic regions.

The Shemshak Group at Shahmirzad (northern Iran) is characterized by the most frequent and extensive marine intercalations and contains the most abundant and diverse ammonite faunas hitherto known from the Lower and lower Middle Jurassic strata of the Alborz Range. So far, 62 ammonite taxa have been recorded from this area, including 25 taxa from earlier studies. The taxa belong to the families Cymbitidae, Echioceratidae, Amaltheidae, Dactylioceratidae, Hildoceratidae, Graphoceratidae, Hammatoceratidae, Erycitidae, and Stephanoceratidae with the new species Paradumortieria elmii and Pleydellia (P. ?) ruttneri. The fauna represents the Late Sinemurian, Late Pliensbachian, Toarcian, Aalenian, and Early Bajocian. Palaeobiogeographically, it is closely related to the Northwest European (Subboreal) Province, and exhibits only minor relations with the Mediterranean (Tethyan) Province.

A new preservation of aptychi is described from the Valanginian limestone-marl alternations of the Vergol section (Drôme), located in the Vocontian Basin (SE France). Aptychi are arranged into two parallel rows which are generally 50 mm in length and separated by 4 mm. The alignments are very often made by entire aptychi (around 10 mm in length), oriented following their harmonic margin. Aptychi show the outside of valve to the viewer: they are convex-up. This fossilization of aptychi is successively interpreted as the result of post-mortem transport by bottom currents (taphonomic-resedimentation process) or the residues (bromalites: fossilized regurgitation, gastric and intestinal contents, excrement) from the digestive tract of an ammonoid-eater (biological processes). Both the parallel rows of aptychi are more likely interpreted as a coprolite (fossil faeces) and they could be considered as both halves (hemi-cylindrical in shape) of the same cylindrical coprolite which would have been separated in two parts (following the long axis) just after the animal defecated. Considering this hypothesis, a discussion is proposed on the hypothetical ammonoid-eater responsible for them.

According to one hypothesis, the exopods of extinct lamellipedian arthropods functioned as gills. To evaluate this hypothesis, the growth rates in Limulus polyphemus for total gill surface, average area per single gill lamella and number of gill lamellae are documented. The rates are compared with corresponding rates in decapod crustaceans in order to make deductions on morphological constraints in multi-foliated gills. The growth rates are given as allometric scaling exponents relative to the animal dry-body weight. The comparisons reveal that each allometric exponent is similar among examined species irrespective of differences in gill morphology or animal body plans. The numerical growth of lamellae obviously is much smaller than the growth of the total respiratory surface. To fulfill these trends in multi-foliated gills, the overall profile tends to become conical, with the result that the surface area is a couple of magnitudes larger at the base of the cone than at the tip. This geometrical shape appears to keep the numerical value of the total respiratory area (total lamellar surface) proportional to the cube of the total number of lamellae. The situation is entirely different in animals with lamellipedian exopods. In the latter, lamellae are slender structures carried in a straight row and, as exemplified by Naraoia, their increase in number during the growth is only half that required for the exopod lamellae to have functioned as an arthropod multi-foliated gill cone.

Onychodictyon ferox, from the Lower Cambrian Chengjiang Lagerstätte, is a worm-like armored lobopod with 10 pairs of dorsal plates and a pair of probable sensory appendages (“antennae”). Newly discovered complete specimens show that Onychodictyon is represented by two species: O. ferox with a “head” bearing a pair of dorsal “antennae” and a trunk with 11 pairs of limbs, whereas O. gracilis has a blunt anterior end without any appendages and a trunk with 12 pairs of limbs. Because of the close resemblance of the “antennae” of O. ferox and those of the lobopod Miraluolishania, they are considered to be homologous structures. The “antennae” of Cambrian lobopodians are proposed to be homologous with the arthropod antennulae.

Six well exposed mid-Ludlow stromatoporoid-dominated reef biostromes in four localities from the Hemse Group in southeastern Gotland, Sweden comprise a stromatoporoid assemblage dominated by four species; Clathrodictyon mohicanum, “Stromatopora” bekkeri, Plectostroma scaniense, and Lophiostroma schmidtii. All biostromes investigated in this area (of approximately 30 km²) are interpreted to belong to a single faunal assemblage forming a dense accumulation of fossils that is probably the best exposed stromatoporoid-rich deposit of the Silurian. The results from this comprehensive study strengthen earlier interpretations of a combination of genetic and environmental control on growth-forms of the stromatoporoids. Growth styles are similar for stromatoporoids in all six biostromes. Differences in biostrome fabric are due to variations in the degree of disturbance by storms. The uniformity of facies and the widespread low-diversity fauna support the view that palaeoenvironmental conditions were similar across the area where these biostromes crop out, and promoted the extraordinary growth of stromatoporoids in this shallow shelf area.

Megalospheric forms of Priabonian Spiroclypeus of the Western Tethys were morphometrically investigated. Based on the reduction of the average number of undivided, post-embryonic chambers, the investigated populations are grouped into two successive, phylogenetically linked species, S. sirottii sp. nov. and S. carpaticus. The evolution is also demonstrated by the increase of the number of secondary chamberlets in particular chambers, by the increase of the diameter of the first two whorls and by that of the size of the proloculus, although the latter turned out to be also ecologically controlled. This evolution is supported by the stratigraphic succession of populations in the Mossano section (N Italy) and by the change of accompanying fossils. Lacking in upper Bartonian beds, the first appearance of genus Spiroclypeus seems to be synchronous with the beginning of the late Eocene. The newly described S. sirottii is associated with Heterostegina reticulata mossanensis and orthophragmines containing forms of middle Eocene acme, both marking the lower part of the Priabonian. Meanwhile S. carpaticus co-occurs with H. gracilis and/or with orthophragmines characteristic of the upper part of the Priabonian. We suppose that the Spiroclypeus sirottii-carpaticus lineage is restricted to the Priabonian. Thus, Spiroclypeus sirottii is a zonal marker for the Shallow Benthic Zone (SBZ) 19 (early Priabonian) while S. carpaticus indicates the SBZ 20 (late Priabonian).

Megalospheric forms of Western Tethyan late Bartonian to late Priabonian involute Heterostegina from numerous localities, marking different ecological conditions, were morphometrically investigated. They belong to three species, H. armenica, H. reticulata, and H. gracilis based on the presence/absence of granulation, on the chamberlet characteristics and on the relative size of proloculus. Within these species a very rapid evolution could be observed in the reduction of the number of operculinid chambers, in the increase of the number of chamberlets and partially in the increase of the proloculus size. This evolution is demonstrated by stratigraphic superpositions in several localities (especially in the Mossano section), and is supported also by the change of co-occurring fossils, starting with the disappearance of large-sized Nummulites, then followed by the appearance of the genus Spiroclypeus and then by the disappearance of orthophragmines of middle Eocene acme. Based on the reduction of operculinid chambers, two chronosubspecies of Heterostegina armenica and seven of H. reticulata are defined biometrically (four of them: H. armenica tigrisensis, H. reticulata tronensis, H. r. hungarica, and H. r. mossanensis are introduced here). This allows to subdivide the Shallow Benthic Zone (SBZ) 18 into three and SBZ 19 into two subzones. The extremely rapid evolution of H. reticulata allows to calibrate larger foraminiferal events around the middle/late Eocene boundary. The extinction of large-sized Nummulites seems to be heterochronous in the late Bartonian in having migrated eastward, while the first appearance of Spiroclypeus is shown to be synchronous at the base of the Priabonian. The middle/upper Eocene (= Bartonian/Priabonian) boundary is to be placed at the base of the Priabona marls in the Mossano section corresponding to the SBZ 18/19 limit, to the first appearance of genus Spiroclypeus, to that of Nummulites fabianii and of Heterostegina reticulata mossanensis. It falls into the upper part of both the P 15 and NP 18 planktic zones. The Western Tethyan Eocene involute Heterostegina became extinct, apparently with no Oligocene successors.

Gastroliths (stomach stones) are known from many extant and extinct vertebrates, including dinosaurs. Reported here is the first unambiguous record of gastroliths in an ornithopod dinosaur. Clusters of small stones found in the abdominal region of three articulated skeletons of Gasparinisaura cincosaltensis were identified as gastroliths on the basis of taphonomic and sedimentologic evidence. The large number of stones found in each individual, their size, and the fact that Gasparinisaura cincosaltensis was herbivorous, all suggest that they were ingested as a result of lithophagy rather than accidental swallowing.