Juvenile specimens of Pinacosaurus grangeri Gilmore, 1933 (Ornithischia: Ankylosauria) from the Late Cretaceous of China, with comments on the specific taxonomy of Pinacosaurus

Four juvenile specimens referable to Pinacosaurus grangeri (Ankylosauria: Dinosauria) are described from the Campanian (Upper Cretaceous) locality Bayan Mandahu in northern Inner Mongolia Autonomous Region (People’s Republic of China). All the specimens preserve the skulls as well as, in some cases, mandibles, postcrania, and osteoderm. They are not taphonomically deformed by expanding matrix distortion, unlike many Gobi specimens, including the holotype of P. grangeri. Bayan Mandahu is also the type locality for Pinacosaurus mephistocephalus. The proximity in space and time of these two closely related species warrants a generic and specific revision for Pinacosaurus. The distinction of the two species is based on characters of the squamosal dermal elaborations, cranial roof posterior to the orbits, premaxillary notch, and distal margin of the ilium. Although a relatively well-represented ankylosaur taxon, the phylogenetic position of Pinacosaurus has not been unequivocally resolved. A new analysis recovers Pinacosaurus as the most basal member of the Ankylosaurinae.     

The status of Dollodon and other basal iguanodonts (Dinosauria: Ornithischia) from the Lower Cretaceous of Europe

Dollodon bampingi was recently named based upon a specimen from the Bernissart Quarry that had previously been referred to Mantellisaurus atherfieldensis. The initial diagnosis of Dollodon did not adequately distinguish it from Mantellisaurus or from other basal iguanodonts, necessitating a reassessment of the material. Firsthand examination of the holotypes of the two taxa and numerous other basal iguanodont specimens, as well as a principal components analysis of basal iguanodont dentaries, did not find any morphological features to justify the distinction of Dollodon from Mantellisaurus. D. bampingi is thus best considered a junior synonym of M. atherfieldensis. Furthermore, the recent referral of the species Iguanodon seelyi to the genus Dollodon is not supported; I. seelyi is indistinguishable from Iguanodon bernissartensis, and is considered a junior synonym of that species. Finally, the recently named taxon Proplanicoxa galtoni, also based upon a specimen formerly attributed to M. atherfieldensis, is considered a nomen dubium and probable junior synonym of M. atherfieldensis. Thus, only two species of large-bodied basal iguanodont should be recognized from the Barremian-Aptian of England and Belgium: M. atherfieldensis and I. bernissartensis.     

A new record and cuticular structure of Meyeria magna (Decapoda,Mecochiridae) from the lower Albian (Lower Cretaceous) of Colombia

Eleven specimens of the lobster Meyeria magna from the Simití Formation (Santander Province, Colombia) represent a new occurrence for this species in South America. Ammonites collected both below and above the bed that yielded M. magna allow dating of these specimens as early Albian. Morphological characteristics observed in these Colombian specimens were compared with those of other specimens from Mexico, the United Kingdom and Spain. Our interpretation of the cuticular structure in thin section does not unambiguously allow interpretation of the specimens studied to corpses or molts.     

An illustrated guide to the fossil barnacles (Cirripedia) from the Crags (Plio-Pleistocene) of East Anglia

The Plio-Pleistocene Crag deposits of East Anglia include a wealth of shelly remains, including barnacles, preserved variously as complete shells, their disarticulated plates and trace fossils. Herein, we present a field guide to these distinctive fossils, with diagnoses of all known taxa recorded from the Crags of East Anglia, supported by both line drawings and photographs. The known stratigraphic and geographic distribution within the study area are tabulated. Recognised species include the sessile barnacles Armatobalanus bisulcatus (Darwin), A. dolossus (Darwin), Balanus balanus (Linné), B. crenatus Bruguière, B. inclusus Darwin, Concavus concavus (Bronn), Chirona hameri (Ascanius), Megabalanus tintinnabulum (Linné), Conopea calceola (Ellis), Co. spongicola (Brown), Acasta undulata Darwin, Coronula barbara Darwin, Megatrema anglicum (G.B. Sowerby) and Verruca stroemia (Müller) (=14 species); two pedunculate forms, Scalpellum magnum Darwin and Lepas delicatula Withers; and the boring Rogerella isp. The greatest diversity of species is found in the Coralline Crag and Red Crag formations, both yielding 11 species, although only four are common to both. Barnacles are poorly represented in other Crag deposits.     

Neoichnology and implications for stratigraphy of reworked Upper Oligocene oysters,Antigua, West Indies

The Late Oligocene oyster Hyotissa antiguensis (Brown) is locally common in the Antigua Formation of Hughes Point, eastern Antigua, Lesser Antilles; it was not commonly bored at that time. Its valves and shells are robust, and reworked into the shallow water near-shore environment in Antigua; it could potentially be incorporated into younger rocks. Its neoichnology includes clues that would facilitate identification of these oysters as reworked fossils. The suite of modern borings found in these specimens includes common Caulostrepsis taeniola Clarke, Gastrochaenolites isp. cf. G. turbinatus Kelly and Bromley and Entobia isp., and rare Oichnus simplex Bromley and Rogerella? isp. The latter three taxa are limited to oyster shell substrates. Of the common ichnotaxa, Caulostrepsis and Gastrochaenolites are particularly prominent in limestone clasts and limestone cemented to oyster shells, which would be an indicator of reworking if found in a post-Oligocene lithified deposit. Caulostrepsis and Gastrochaenolites are relatively less common in oyster shells and valves, and in many specimens are seen to terminate against the shell. Entobia is the only common boring limited to the shell substrate. The fidelity of preservation of modern borings is also superior in limestone clasts. This suite of borings is comparable with those found in the Neogene of the Antillean region.     

Leptolepid otoliths from the Hauterivian (Lower Cretaceous) Lower Weald Clay (southern England)

Teleostean saccular otoliths from the upper part of the late Hauterivian Lower Weald Clay Formation of the Wealden Supergroup exposed at Langhurstwood Quarry, West Sussex, UK, and Clockhouse Brickworks, Surrey, UK are described for the first time. Two new species of the genus Leptolepis, Leptolepis wealdensis and Leptolepis toyei are described. Many of the specimens are densely packed on individual bedding planes and they are interpreted as coprocoenotic accumulations. Additional mechanisms of deposition and concentration are discussed, in particular wave action. Ontogenetic series show isometric growth of the otoliths, and some specimens show growth rings on two orders of magnitude.     

Latest Pleistocene paleoecology of Jefferson's ground sloth (Megalonyx jeffersonii) and elk-moose (Cervalces scotti) in northern Illinois

New records of Jefferson's ground sloth (Megalonyx jeffersonii) and elk-moose (Cervalces scotti) from Lang Farm provide the first precise temporal correlation of these taxa with the specific environments inhabited by them near the time of their extinction. Six AMS ¹⁴C measurements establish an age of 11,405 ± 50 ¹⁴C yr B.P. for Lang Farm Cervalces and an age of 11,430 ± 60 or 11,485 ± 40 ¹⁴C yr B.P. for the Megalonyx. These measurements represent the youngest ¹⁴C dates for these two genera based on direct dating. Comparison of the dates with pollen data from northern Illinois indicates that these species inhabited a nonanalog environment that was transitional from mid-latitude tundra to mixed conifer and deciduous woodland. Although spruce (Picea sp.) was dominant, it was less abundant than prior to 12,500 ¹⁴C yr B.P. The presence of black ash (Fraxinus nigra) and fir (Abies sp.) indicates a wet climate and heavy winter precipitation. This may have been the preferred habitat for Cervalces because of its narrow geographic range. However, this habitat type was only one of many occupied by Megalonyx as indicated by its broad geographic distribution.     

Possible animal body fossils from the Late Neoproterozoic interglacial successions in the Kimberley region, northwestern Australia

New specimens of the enigmatic Ediacara-type fossil Palaeopascichnus have been identified from the upper part of the Neoproterozoic Ranford Formation in the Kimberley region, northwest Australia. New material is morphologically similar to Palaeopascichnus and represents the largest species of this genus. They resemble the present-day xenophyophore protists in chamber morphology and growth patterns, supporting the interpretation that Palaeopascichnus is possibly a xenophyophore body fossil rather than a trace fossil. Stratigraphic correlation reveals that the new Palaeopascichnus specimens are preserved in the interglacial successions between the Landrigan/Marinoan and Egan/Ediacaran glaciations. If correlation with the early Ediacaran formations of South Australia is accepted, this represents the earliest known identifiable member of the Ediacara biota. New fossil record fills the evolutionary gap between the Cryogenian and Ediacaran animal assemblages and well-known Ediacaran biota. The new Palaeopascichnus specimens represent the first record of Ediacara-type fossils in Kimberley, and suggest the probability that additional Ediacaran fossils may be found in northwestern Australia.     

Pachycephalosaurs (Dinosauria: Ornithischia) from the Upper Cretaceous (upper Campanian) of New Mexico: A reassessment of Stegoceras novomexicanum

Pachycephalosaurs, a group of ornithischian dinosaurs with distinctive cranial ornamentation and skull domes, underwent dramatic changes in cranial morphology during ontogeny. This has caused debate about whether some specimens belong to juveniles or adults, which impacts studies of pachycephalosaur phylogeny and evolution. One such debate concerns a small skull roof specimen from the Campanian (Upper Cretaceous) of New Mexico, NMMNH P-33898, which was originally described as an indeterminate juvenile but later regarded as a mature adult and erected as the holotype of a new small-bodied species, Stegoceras novomexicanum. We restudied NMMNH P-33898 using computed tomography scanning, morphometric and phylogenetic analyses, and comparisons to growth series of other pachycephalosaurs (Stegoceras validum, Pachycephalosaurus wyomingensis). We conclude that two purported paratype specimens of Stegoceras novomexicanum cannot be referred to the same taxon as the holotype, that the holotype and controversial paratypes all belong to immature specimens and not aberrant small-bodied adults, but that current evidence cannot clearly determine whether NMMNH P-33898 is a juvenile belonging to its own diagnostic species (S. novomexicanum) or is a juvenile of Stegoceras validum, Sphaerotholus goodwini, or another known taxon. We review the pachycephalosaur record of New Mexico and demonstrate that pachycephalosaurs were important components of dinosaur faunas in the southern part of Western North America during the ∼15 million years before the end-Cretaceous extinction, just as they were in roughly contemporaneous northern localities.     

The Late Pleistocene distribution of vicuñas (Vicugna vicugna) and the “extinction” of the gracile llama (“Lama gracilis”): New molecular data

We present the results of a palaeogenetic analysis of two Late Pleistocene camelids originating in southern Chile. Our analysis of two mitochondrial DNA fragments (control region and cytochrome b gene) reveals that these specimens do not belong to an extinct taxon, but rather to extant vicuña (Vicugna vicugna), whose modern distribution is restricted to the extreme elevations of the Andes, more than 3500 km to the north of where these specimens originated. Our results also suggest fossil specimens from Patagonia that are currently assigned to the extinct taxon Lama gracilis, may actually belong to V. vicugna, implying a continuous distribution of the latter from the southern tip of South America to the Andes during the Final Pleistocene. The haplotypes of both specimens are not present in modern populations, suggesting a loss of genetic diversity concomitant with the contraction of the vicuña geographical distribution during the Final Pleistocene or early Holocene.     

Teredolites Leymerie in the Lower Greensand Group (Cretaceous) of the Isle of Wight and the problematic ichnology of reworked clasts

Nineteenth-century references to clavate borings in woody substrates in the Lower Greensand of the Isle of Wight used a variety of names, but Teredo (a wood-boring bivalve, not a boring), Teredolithes (a junior synonym of Teredolites) and Gastrochaena (a bivalve borer of rock and shelly substrates, not a boring in wood) are all nomenclatorially incorrect. Borings in a beach clast derived from the Lower Greensand Group and recently collected from Sandown Bay, Isle of Wight, are referred to Teredolites isp. cf. T. longissimus Kelly and Bromley. This specimen confirms the presence of Teredolites in the Lower Greensand Group and demonstrates a common ichnological problem of beach clasts; borings, either fossil or modern, are incompletely preserved, making confident classification below the level of ichnogenus problematic.     

New remains of Eremotherium laurillardi (Lund, 1842) (Megatheriidae,Xenarthra) from the coastal region of Ecuador

New remains of Eremotherium were recovered from the Pacific coast of Ecuador’s Manabi province. The Machalilla fossiliferous locality records the northernmost presence of Eremotherium along the Pacific coast of South America. Most of the fossil remains belong to the same individual, mainly its posterior half, but other individuals are represented. Among the better-preserved specimens are skull fragments, most of the hind limb bones and a number of trunk and caudal centra. These remains were compared with samples collected during the 20th century along the southern coastal regions of Ecuador and northern Peru. Many characters of the long bones and tarsals testify to a possibly different lineage despite the closeness of other Eremotherium populations. Some metric and morphological aspects suggest a different space-temporal southern Caribbean provenance. Other Eremotherium specimens, coming from other Ecuadorian localities, were studied and compared with classic Eremotherium samples. Interesting morpho-functional aspects are pointed out with regard to the tail and its importance in the bipedal stance.     

A new approach to the Late Miocene-Early Pliocene forms of the genus Apocricetus. Apocricetus alberti (Rodentia,Mammalia) from Venta del Moro (Cabriel Basin,Spain)

The species of the genus Apocricetus are considered to form the phyletic lineage A. aff. plinii (MN11)–A. plinii–A. alberti–A. barrierei–A. angustidens (MN16). Along this lineage, gradual morphological and biometrical changes occur, but not all the species are represented by rich populations. The assemblage of Apocricetus alberti from Venta del Moro is by far the most abundant collection of this species. This population shows a great morphological variability in some characters like the morphology of the anteroconid and the anterolophulids in m1 and the shape of the anterolophule in M1, with morphotypes that resemble both older and younger populations of Apocricetus. Along the phyletic lineage of Apocricetus, a change in the shape of m3 occurs, from predominantly subtriangular forms in the oldest populations to predominantly subrectangular in the youngest. To quantify this feature we use the posterior width of the molar and the anterior width/posterior width ratio, proposing five morphological categories, from extremely triangular to subrectangular.     

Use of CART analysis to differentiate pollen of red pine (Pinus resinosa) and jack pine (P. banksiana) in New England

The identification of fossil pollen at the generic rather than species level is hampering progress in understanding the biogeography and dynamics of paleo-vegetation. We used CART analysis to facilitate the differentiation of fossil pollen of Pinus banksiana and Pinusresinosa, which are morphologically similar and nearly always combined in paleoecological studies. The CART model, using four of the ten morphological traits measured, exhibited a high level of correct identification for pollen of each of the species and shows promise as a tool for increasing the detail of paleoecological records and inferences.     

Platyceratid gastropod infestations of Neoplatycrinus Wanner (Crinoidea) from the Permian of West Timor: speculations on thecal modifications

Distinctive trace fossils, indicating the infestation of the monobathrid camerate crinoid Neoplatycrinus Wanner by coprophagous platyceratid gastropods, are recognised for the first time from the Permian of West Timor. Platyceratid shells from West Timor have previously been reported preserved on or about the crinoid tegmen, that is, apically; in contrast, the trace fossils described herein occur in the CD interray (=posteriorly), mainly on the radials. There are two patterns of infestation in the CD interray. Circular grooves in this position, situated below the periproct, are referred to Lacrimichnus isp. Thecal modifications include the CD interray sloping towards the base, and incomplete curved ridges developed outside the circular groove and confined to the radials. A different morphology is shown by other specimens that have a broad, flattened CD interray, curving down to and extending onto the basals; this interray also slopes towards the base. These unusual CD interray modifications are interpreted as a product of snail/crinoid associations. We speculate that the major modifications to the theca may have permitted the platyceratid shell to mimic an uninfested CD interray and thus maintain the hydrodynamic integrity of the crown. This would have been to the advantage of both gastropod and crinoid. The camerates did not survive the P/Tr extinction; their demise ended an association that had persisted over 200 million years, although the platyceratids persisted into the Mesozoic.