A new actinomycete from a Guadalupian vertebrate coprolite from Brazil

Coprolites (fossil feces) are important sources of evidence of ancient food webs and ecosystems. Actinomycetes are a fundamental component in the decay of organic matter, and serve as catalysts for nutrient cycles. Recently, gas vesicles filled with numerous verrucose colonies of substrate mycelium of an actinomycete were discovered inside a fossilized spiral amphipolar fish coprolite recovered from mid–Permian deposits of Brazil. These colonies are composed of masses of substrate hyphae, some of which are undergoing segmentation. Arising from the colonies are chains of spores separated by narrow, elongate connectives. The fossil actinomycete is described below as Palaeostromatus diairetus gen. et sp. nov. and represents the oldest known actinomycete associated with vertebrate deposits. Since the colonies occur only inside the coprolite, either Palaeostromatus diairetus gen. et sp. nov. was part of the gut flora or it was acquired from a food source. The only other remains in the coprolite are eighteen paleoniscoid fish scales, which suggests that the producer was a carnivorous/omnivorous fish. This is the oldest record of a direct interaction between vertebrates and actinomycetes.     

Scontrone (central Italy), signs of a 9‐million‐year‐old tragedy

The fossilierous bonebeds of Scontrone (Abruzzo region, central Italy) are preserved in tidal‐flat aeolian calcarenites at the base of the Lithothamnion Limestone, a Miocene carbonate ramp widespread in the central‐southern Apennines. The site bears evidence of a catastrophic event at 9 Ma. Reported are the results of the palaeobiological and taphonomic analysis conducted on the rich vertebrate assemblage, particularly on the remains of Hoplitomeryx (Mammalia, Artiodactyla, Ruminantia), recovered from the so‐called Scontrone calcarenites between 1992 and 2012. This is the first taphonomic study of a Late Miocene continental bone assemblage preserved in coastal deposits. The bones are not in primary context. They were likely exhumed during the initial phase of a marine transgression after a period of primary ‘storage’ within a possibly flood‐generated deposit in an estuarine environment. The mortality patterns indicate that the carcasses accumulated in a short time (within a year). The bones of the disarticulated skeletons were then removed, broken in a dry and brittle state, scattered over wide carbonate ramps along an arid to semi‐arid, wind‐exposed coastline and eventually buried again in aeolian calcarenites that drape transgressive tidal‐flat creek deposits. The analysis also reveals that hoplitomerycids were possibly seasonal reproducers and that the land they inhabited, the so‐called Apulia Platform, was probably swept by sudden, disastrous, storm‐supplied flash floods.     

Late Cretaceous bioconnections between Indo‐Madagascar and Antarctica: refutation of the Gunnerus Ridge causeway hypothesis

Aim To evaluate the Gunnerus Ridge land‐bridge hypothesis, which postulates a Late Cretaceous causeway between eastern Antarctica and southern Madagascar allowing the passage of terrestrial vertebrates. Location Eastern Antarctica, southern Indian Ocean, Madagascar. Methods The review involves palaeogeographical modelling, which draws upon geological and geophysical data, bathymetric charts, and plate tectonic reconstructions, and the evaluation of stratigraphically calibrated phylogenetic analyses to document ghost lineages of select taxa. Results The available geological and geophysical evidence indicates that eastern Antarctica’s Gunnerus Ridge and southern Madagascar were separated for the entire Late Cretaceous by a vast marine expanse. In the mid–Late Cretaceous, the gap was probably punctuated by land on two intervening physiographical highs, the northern Madagascar Plateau and Conrad Rise, the latter of which, although probably large, was still separated from Antarctica’s Riiser‐Larsen Peninsula by c. 1600 km. Recent, stratigraphically calibrated phylogenies including large, terrestrial end‐Cretaceous vertebrate taxa of Madagascar and the Indian subcontinent reveal long ghost lineages that extended into the Early Cretaceous. Main conclusions The view that Antarctica and Madagascar were connected by a long causeway between the Gunnerus Ridge and southern Madagascar in the Late Cretaceous, and that terrestrial vertebrates were able to colonize new frontiers using this physiographical feature, is almost certainly incorrect, as was previously demonstrated for the purported causeway between Antarctica and the Indian subcontinent across the Kerguelen Plateau. Connection across mainland Africa to account for the close relationships of several fossil and extant vertebrate taxa of Indo‐Madagascar and South America is another option, although this too lacks credibility. We conclude that (1) throughout the Late Cretaceous there was no intervening, continuous causeway through Antarctica and associated land bridges between South America to the west and Indo‐Madagascar to the east; and (2) mid‐ to large‐sized, obligate terrestrial forms (e.g. abelisauroid theropod and titanosaurian sauropod dinosaurs and notosuchian crocodyliforms) gained broad distribution across Gondwanan land masses prior to fragmentation and were isolated on Indo‐Madagascar before the end of the Early Cretaceous.     

Multi‐proxy analyses of Late Cretaceous coprolites from Germany

A total of 462 coprolites from three localities exposing Upper Cretaceous deposits in the Münster Basin, northwestern Germany, have been subjected to an array of analytical techniques, with the aim of elucidating ancient trophic structures and predator–prey interactions. The phosphatic composition, frequent bone inclusions, size and morphology collectively suggest that most, if not all, coprolites were produced by carnivorous (predatory or scavenging) vertebrates. The bone inclusions further indicate that the coprolite producers preyed principally upon fish. Putative host animals include bony fish, sharks and marine reptiles – all of which have been previously recorded from the Münster Basin. The presence of borings and other traces on several coprolites implies handling by coprophagous organisms. Remains of epibionts are also common, most of which have been identified as the encrusting bivalve Atreta. Palynological analyses of both the coprolites and host rocks reveal a sparse assemblage dominated by typical Late Cretaceous dinoflagellates, and with sub‐ordinate fern spores, conifer pollen grains and angiosperm pollen grains. The dinoflagellate key taxon Exochosphaeridium cenomaniense corroborates a Cenomanian age for the Plenus Marl, from which most studied coprolites derive. The findings of this study highlight the potential of a multi‐proxy approach when it comes to unravelling the origin, composition and importance of coprolites in palaeoecosystem analyses.     

Coprolite morphotypes from the Upper Cretaceous of Sweden: novel views on an ancient ecosystem and implications for coprolite taphonomy

Eriksson, M.E., Lindgren, J., Chin, K. & Månsby, U. 2011: Coprolite morphotypes from the Upper Cretaceous of Sweden: novel views on an ancient ecosystem and implications for coprolite taphonomy. Lethaia, Vol. 44, pp. 455–468. Coprolites (fossilized faeces) are common, yet previously unreported, elements in the Campanian (Upper Cretaceous) shallow‐marine strata of Åsen, southern Sweden. They are associated with a diverse vertebrate fauna and comprise at least seven different morphotypes that suggest a variety of source animals. Their faecal origin is corroborated by several lines of evidence, including chemical composition (primarily calcium phosphate), external morphology and nature of the inclusions. Preservation in a fossil coquina, interpreted as a taphocoenosis, suggests early lithification promoted by rapid entombment. This would have prevented disintegration of the faecal matter and facilitated transportation and introduction to the host sediment. The coprofabrics can generally be correlated to specific gross morphologies, supporting a morphology‐determined coprolite classification. Moreover, having been deposited under presumably comparable taphonomic conditions, variations in coprofabrics infer differences in diet and/or digestive efficiency of the host animal. Size and morphology of the coprolites imply that most, if not all, were produced by vertebrates and the largest specimens infer a host animal of considerable size. Two spiralled coprolite morphotypes yield bone fragments and scales of bony fish, suggesting that the producers were piscivorous sharks. Other coprolites contain inclusions interpreted as the remains of shelled invertebrates, thus indicating that they may have derived from durophagous predators and/or scavengers. The occurrence of small scrapes, tracks and traces on several specimens suggest manipulation of the faeces by other (presumably coprophagous) organisms after deposition. The collective data from the Åsen coprolites provide new insights into a shallow‐water Late Cretaceous marine ecosystem hitherto known solely from body fossils. □ Coprolites, vertebrates, coprofabrics, taphonomy, trophic levels, Upper Cretaceous, Sweden.     

First record of Mesozoic scroll coprolites: classification,characteristics, elemental composition and probable producers

Multiple, small, cylindrical scroll coprolites having rounded and tapering ends and pertaining to a new ichnotaxon have been recovered from the Upper Triassic Tiki Formation of India. This is the first record of scroll coprolites from the Mesozoic. Based on cross‐sectional geometry, external surface textures, and internal morphology, these coprolites are subdivided into three morphotypes. The coprolites contain several kinds of undigested food material in the form of ganoid fish scales, teeth, lower jaw and skeletal remains of various osteichthyans, chondrichthyans, archosauriforms and indeterminate reptiles. These inclusions are embedded in the groundmass separated by thin mucosal layers. The groundmass contains abundant gas vesicles, and secondarily‐filled shrinkage cracks. EDS analysis shows that the overall composition of the coprolites reflects Ca, P, C and O, suggesting calcium phosphate mineralogy, though other elements such as Fe, Mn, Al, Si are present in lesser proportions. Based on their similarity with the scrolled faeces of extant euryhaline hammerhead sharks, it is deduced that these coprolites were produced by euryhaline hybodontid sharks. At least two hybodontid taxa, Lonchidion and Pristrisodus, show high prevalence in the Tiki vertebrate fauna, suggesting that these were the possible producers. As the coprolite inclusions contain remains of other aquatic animals, these carnivorous hybodonts constituted the dominant predators of the Tiki aquatic ecosystem.     

Microbiota and food residues including possible evidence of pre‐mammalian hair in Upper Permian coprolites from Russia

Coprolites (fossil faeces) provide direct evidence on the diet of its producer and unique insights on ancient food webs and ecosystems. We describe the contents of seven coprolites, collected from the Late Permian Vyazniki site of the European part of Russia. Two coprolite morphotypes (A, B) contain remains of putative bacteria, cyanobacteria, fungi, protists, invertebrate eggs, arthropod elements, undigested bone and tooth fragments, fish scales and elongated hair‐like structures with hollow interiors. Content, size and shape of the coprolites together with the associated body fossil record suggest that the most probable scat‐producers were carnivorous tetrapods; the bone‐rich morphotype A reveals short food retention time and a fast metabolism and is therefore assigned to therapsid carnivores whereas morphotype B with rarer and degraded bones are assigned to archosauromorphs or other non‐therapsid carnivores. The general coprolite matrix contains abundant micron‐sized spheres and thin‐walled vesicles which are interpreted as oxide and phosphatic pseudomorphs after microbial cells. From analyses of the undigested bones, we infer that they represent remains of actinopterygian fish, a therapsid and unrecognizable parts of amphibians and/or reptiles. Additionally, hair‐like structures found in one coprolite specimen occur as diagenetically altered (oxide‐replaced) structures and moulds (or partly as pseudomorphs) in a microcrystalline carbonate‐fluoride‐bearing calcium phosphate. This suggests that the latest Permian therapsids probably were equipped with hair‐like integument or hairsuit. If true, this is by far the oldest evidence of this mammalian character in the stem group of mammals.     

Changes in lifestyle and habitat of Zoophycos‐producing animals related to evolution of phytoplankton during the Late Mesozoic: geological evidence for the ‘benthic‐pelagic coupling model’

The trace fossil Zoophycos characterized by complex, three‐dimensional morphology with systematic internal structures occurs throughout the Phanerozoic marine sediments. The specimens of Zoophycos examined herein consist of a downward and helical spreite and are a product of the excretory behaviour of endobenthic detritus feeders. They are divided into two basic types: pre‐Jurassic and post‐Cretaceous types on the basis of whorls of spreiten in a single specimen. The pre‐Jurassic type has fewer than four whorls. In contrast, most of the post‐Cretaceous specimens exhibit spreite with multiple coils more than ten whorls. The abrupt increase in whorl number during the Cretaceous suggests that the sedentary lifestyle of the producer should change from a short‐term stay to long‐term or permanent occupation of the same burrow. Timing of the lifestyle change the Zoophycos producers seems to be closely related to the deep‐seaward migration of their habitats. The change in lifestyle and migration of Zoophycos‐producing animals during the Cretaceous might be attributable to the establishment of eutrophic bottom conditions in the deep sea. These changes seem to be associated with the flux of large amounts of phytodetrital food produced by phytoplankton, which experienced an explosive increase in species diversity during the Late Jurassic to the Late Cretaceous. The series of changes in lifestyle and habitat of the Zoophycos animals during the Late Mesozoic can serve as one piece of geological evidence for the ‘benthic‐pelagic coupling model’.     

依兰-伊通地堑方正断陷孢粉组合及其地层层序

根据大量钻井岩心中的孢粉资料,建立了方正断陷内白晋系至新近系5个孢粉组合,讨论了其地质时代,并结合岩性资料,首次将乌云组和富锦组引入方正断陷,提出了方正断陷不仅发育有古近纪新安村组和达连河组,而且还发育有晚白晋世方正组,古近纪乌云组,宝泉岭组以及新近纪富锦组,进而完善了方正断陷区沉积地层层序。     

Early Triassic coprolites from Australia and their palaeobiological significance

Abstract:  Coprolites from the Arcadia Formation, Queensland, Australia, were studied in conjunction with the vertebrate fossil assemblages from two localities to maximize our understanding of the palaeoecology of these Early Triassic deposits. Criteria used by other researchers to identify the producers of coprolites were found to be of little value in the Arcadia Formation specimens. Using a combination of shape, biostratigraphic distribution, size and included remains some of the coprolites are attributed to basal archosauromorphs and fish whereas others could not be identified. Perhaps the most important attribute of the Arcadia coprolites is that they preserved rare organisms such as cyanobacteria, insects and other arthropods, and a diversity of fish. Estimates of the number of actinopterygians and dipnoans preserved in coprolites significantly increased relative abundance estimates based on skeletal elements alone. Although coprolites are an important source of palaeobiological information, this information is limited by our poor understanding of the taphonomic processes involved in the fossilization of faecal matter and by the near impossibility of assigning coprolites to specific producers.     

BOOM AND BUST: ANCIENT AND RECENT DIVERSIFICATION IN BICHIRS (POLYPTERIDAE: ACTINOPTERYGII), A RELICTUAL LINEAGE OF RAY‐FINNED FISHES

Understanding the history that underlies patterns of species richness across the Tree of Life requires an investigation of the mechanisms that not only generate young species‐rich clades, but also those that maintain species‐poor lineages over long stretches of evolutionary time. However, diversification dynamics that underlie ancient species‐poor lineages are often hidden due to a lack of fossil evidence. Using information from the fossil record and time calibrated molecular phylogenies, we investigate the history of lineage diversification in Polypteridae, which is the sister lineage of all other ray‐finned fishes (Actinopterygii). Despite originating at least 390 million years (Myr) ago, molecular timetrees support a Neogene origin for the living polypterid species. Our analyses demonstrate polypterids are exceptionally species depauperate with a stem lineage duration that exceeds 380 million years (Ma) and is significantly longer than the stem lineage durations observed in other ray‐finned fish lineages. Analyses of the fossil record show an early Late Cretaceous (100.5–83.6 Ma) peak in polypterid genus richness, followed by 60 Ma of low richness. The Neogene species radiation and evidence for high‐diversity intervals in the geological past suggest a “boom and bust” pattern of diversification that contrasts with common perceptions of relative evolutionary stasis in so‐called “living fossils.”     

Tertiary dinosaurs in South America? A reply to some of Van Valen's assertions

The discussion of the age of some South American Late Cretaceous fossil vertebrate localities by Van Valen led this author to admit the possible persistence of Dinosaurs at the base of the Paleocene. Van Valen's arguments resting on the selachians are reviewed and it can be asserted that the selachian‐bearing localities of the El Molino Formation of Bolivia are Cretaceous and not Tertiary.     

Early Cretaceous stratigraphy and SHRIMP U‐Pb age constrain the Valanginian–Hauterivian boundary in southern Tibet

Wan, X., Scott, R., Chen, W., Gao, L. & Zhang, Y. 2011: Early Cretaceous stratigraphy and SHRIMP U‐Pb age constrain the Valanginian–Hauterivian boundary in southern Tibet. Lethaia, Vol. 44, pp. 231–244. The Late Jurassic to the Early Cretaceous marine strata are extensively distributed in southern Tibet. In Gyangze, the strata are divided into the Weimei and Jiabula formations. In Nagarze, they are divided into the Weimei and Sangxiu formations. Previous work has reported diverse ammonite species of Haplophylloceras and Himalayites in the Weimei Formation, and a few species of Spiticeras in the lower Jiabula and Sangxiu formations. The present study has found the bivalve Inoceramus and nannofossil assemblages in the lower Jiabula and Sangxiu formations. The nannofossil assemblage of Nannoconus steimannii steinmannii, N. steinmannii minor and Watznaueria barnesae indicates Berriasian age, and the Calcicalathina oblongata–Speetonia colligata assemblage is Valanginian in age. Numerical ages for the Jiabula and Jiabula‐goukou sections in Gyangze have been interpolated by comparing the fossil ranges with ages calibrated in other sections. The correlation experiment plots fossil ranges in the two sections to the CRET1 Database. The estimated rate of sediment accumulation of the lower Sangxiu Formation is 22.6 m/myr. The Jurassic–Cretaceous (J/K) boundary is at the bottom of the Jiabula Formation in Gyangze, and the base of the Sangxiu Formation in Nagarze. The boundary is marked by the appearance of the ammonite Spiticeras and the nannofossil assemblage of Nannoconus st. steinmannii–N. st. minor–Watznaueria barnesae. The radiometric age in Tibet is the first to be integrated with upper Valanginian fossils. The volcanic rocks of the upper Sangxiu Formation are dated at 136 ± 3.0 Ma deduced from zircon SHRIMP age of rhyolite. By consideration of the rate of sediment accumulation of the underlying sedimentary deposits, the J/K boundary in the Gyangze–Nagarze area is approximately 145 Ma as suggested by the newly issued International Stratigraphic Chart, and the Valanginian/Hauterivian boundary lies between 134 Ma and 136 Ma. □ Biostratigraphy, graphic plot, Jurassic/Cretaceous boundary, nannofossil, SHRIMP U‐Pb age, Southern Tibet, Valanginian/Hauterivian boundary.     

Cretaceous small scavengers: feeding traces in tetrapod bones from Patagonia, Argentina

Ecological relationships among fossil vertebrate groups are interpreted based on evidence of modification features and paleopathologies on fossil bones. Here we describe an ichnological assemblage composed of trace fossils on reptile bones, mainly sphenodontids, crocodyliforms and maniraptoran theropods. They all come from La Buitrera, an early Late Cretaceous locality in the Candeleros Formation of northwestern Patagonia, Argentina. This locality is significant because of the abundance of small to medium-sized vertebrates. The abundant ichnological record includes traces on bones, most of them attributable to tetrapods. These latter traces include tooth marks that provde evidence of feeding activities made during the sub-aerial exposure of tetrapod carcasses. Other traces are attributable to arthropods or roots. The totality of evidence provides an uncommon insight into paleoecological aspects of a Late Cretaceous southern ecosystem.     

Gar-Bitten Coprolite From South Carolina,USA

Coprolites can preserve a wide range of biogenic components. Of all the coprolites known from the fossil record, hitherto only two are known to preserve vertebrate tooth impressions (i.e., those of chondrichthyans). Here, a coprolite, from a thick lag deposit that includes a mixture of late Cretaceous, early Paleocene, and Plio-Pleistocene taxa at Clapp Creek in Kingstree, Williamsburg County, South Carolina, USA, preserves bite marks most consistent with having been made by a gar, Lepisosteus sp. (Lepisosteidae, Actinopterygii). This is the first-known coprolite to preserve actinopterygian tooth/bite marks. Aborted coprophagy seems unlikely; an accidental or serendipitous strike more likely describes the origin of the score marks over the surface of the coprolite. This coprolite also preserves small paired striations interpreted as evidence of coprophagy by an unknown organism.     

Microstructural disparity between basal micrabaciids and other Scleractinia: new evidence from Neogene Stephanophyllia

Recent molecular analyses based on mitochondrial and nuclear markers place the Micrabaciidae in the basal clade of scleractinian corals. The molecular distinctiveness of micrabaciids is supported by a set of unique morphological characters, among which the microstructure of thickening deposits is the most characteristic one. In all extant and well‐preserved Mesozoic micrabaciids (extinct Micrabacia, and still living Letepsammia, Rhombopsammia, Stephanophyllia, Leptopenus), thickening deposits consist of irregular meshwork of small chip‐like bundles of fibres. Here, we document Neogene (Miocene and Pliocene) forms identified as Stephanophyllia whose thickening deposits consist of long and thin parallel fibres that, instead of bundles (like in majority of Scleractinia), form layers of thatch‐like structures that thicken the septa. This microstructural pattern distinguishes Neogene Stephanophyllia from all examined so far micrabaciids and suggests that mechanisms of biologically controlled mineralization within this clade were more diverse. Nonetheless, the group as a whole is still clearly separated microstructurally from other scleractinians. Despite their basal position in scleractinian phylogeny, the fossil record of Micrabaciidae starts only in the Lower Cretaceous. No Palaeozoic, Triassic or Jurassic forms that could be considered ancestral to micrabaciids and would share some microstructural or morphological (e.g. septal insertion pattern) characters have yet been found. Possible explanations of such morphological disparity of micrabaciids from other scleractinians are either sudden emergence by skeletonization of long evolved, soft‐bodied group of basal hexacorallians or migration of their skeletonized, deep‐water ancestors to shallow‐waters.     

Bioclaustration trace fossils in epeiric shallow marine stromatolites: the Cretaceous‐Palaeogene Yacoraite Formation,Northwestern Argentina

The shallow carbonate facies at the top of the Yacoraite Formation (Late Cretaceous–Early Palaeocene) in the Metán sub‐basin, Salta Basin (Cretaceous‐Eocene), northern Argentina, have domal stromatolitic boundstones with peculiar cavities, interpreted here as bioclaustrations. The cavities appear to have been produced by organisms that lived within the microbial mat contemporarily with its growth, producing a distinctive ichnofabric. This is the oldest reported record of bioclaustrations in stromatolites, and the first in shallow marine environments. The interpretation of the facies suggests a stressed shallow, restricted setting with variations in salinity, represented by an intertidal environment with an extensive tidal flat. Bioclaustrations, stromatolites, endobiont Yacoraite Formation (Cretaceous‐Palaeogene), Northwestern Argentina.     

Fossil bee nests,coleopteran pupal chambers and tuffaceous paleosols from the Late Cretaceous Laguna Palacios Formation,Central Patagonia (Argentina)

The Late Cretaceous Laguna Palacios Formation in Central Patagonia (San Jorge Basin), southern South America, is composed of tuffaceous deposits supplied by periodical volcanic ash falls partly reworked by rivers, on broad plains. Variations in ash-fall rates allowed the formation of stacked, mature paleosols, which are one of the most characteristic features of this formation. The mature paleosols show well-developed horizons, ped structure and bear an intricate network of trace fossils mostly produced by small roots and invertebrates. Two different insect trace fossils could be recognized in this formation: sweat bee nests and coleopteran pupal chambers. Fossil bee nests are composed of inclined tunnels with cells attached to them by means of short necks, a typical construction of bees of the subfamily Halictinae. Similar halictine constructions were reported from the Cretaceous of the USA. Coleopteran pupal chambers are discrete, ovoid structures, having an internal cavity with a smooth surface, and an outer wall of lumpy appearance composed of different layers of soil material. They are commonly constructed by the larvae of different families of Coleoptera. Similar trace fossils were previously reported from the Asencio Formation (Late Cretaceous–Early Tertiary) of Uruguay and from the Djadokhta Formation of Mongolia (Late Cretaceous). These trace fossils constitute some of the only paleontological data from the Laguna Palacios Formation, allowing inferences about its paleoecology, paleoclimatology and paleogeography. Ecological preferences of Halictinae, as well as some features of the nests, suggest a temperate, seasonal climate and an environment dominated by low vegetation for the Laguna Palacios Formation, which is also compatible with sedimentologic and pedogenic evidence. The morphology of the nests, typical of North American halictinae, adds more evidence to the hypothesis of the existence of faunal interchange between North and South America by the Late Cretaceous. The fossil nests constitute some of the oldest evidence of bees in the fossil record, the third known record of bees of Cretaceous age and the first for the Southern Hemisphere. The two traces described are, together with those of Dakota and the Gobi Desert, the only trace fossils from paleosols of Cretaceous age that can be certainly attributed to insects.     

The West Gondwanan Occurrence Of The Hybodontid Shark Priohybodus, And The Late Jurassic–Early Cretaceous Age Of The Tacuarembó Formation, Uruguay

Priohybodus cf. P. arambourgi is reported for the first time from the Tacuarembó Formation of Uruguay. This species is a hybodontid shark known previously only from Upper Jurassic and Lower Cretaceous deposits of Saharan Africa and the Arabian Peninsula. The material (22 isolated teeth and a dorsal fin spine) was found in a thin bone bed, associated with abundant bone fragments, scales and teeth of semionotiform fishes and theropod dinosaurs. Until now, the age of the Tacuarembó Formation has been difficult to determine because its fossil content lacked useful biostratigraphic indicators. The finding of Priohybodus cf. P. arambourgi in that unit greatly expands the palaeobiogeographic range of the species, and allows us to propose a Late Jurassic–Early Cretaceous age for the Tacuarembó Formation.     

辽宁凌源及内蒙古宁城地区下白垩统义县组脊椎动物生物地层

辽宁凌源及相邻内蒙古南部宁城地区义县组发现多个重要脊椎动物化石地点,通过岩 石地层、脊椎动物生物地层和同位素年代地层对比,建立了该地区义县组地层层序。凌源一宁 城地区义县组有 ２个脊椎动物化石层位：下部道虎沟层含 Ｌｙｃｏｐｔｅｒａｅｒ Ｉｃｈｔｈｙｏｆａｕｎａ, Ｐｓｉｔｔａｃｏｓａｕｒｕｓ Ｆａｕｎａ和Ｃｏｎｆｕｃｉｕｓｏｒｎｉｓ Ａｖｉｆａｕｎａ等３个动物群,可以与北票尖山沟层的四合 屯脊椎动物化石群对比,层位相当于义县组一、三段;上部大王杖子（大新房子）层含 Ｌｙｃｏｐｔｅｒａ Ｉｃｈｔｈｙｏｆａｕｎａ和Ｌｉａｏｘｉｏｒｎｉｓ Ａｖｉｆａｕｎａ等２个动物群,为义县组中部沉积,在四合屯地 区缺失。冀北丰宁四岔口－森吉图地区义县组脊椎动物化石层对应于凌源大王杖子层;滦平 大北沟组为义县组最下部沉积,其上覆的大店子组相当于宁城道虎沟层和北票四合屯义县组 一、三段。热河群义县组和九佛堂组发现３个连续的鸟类群;义县组下部Ｃｏｎｆｕｃｉｕｓｏｒｎｉｓ Ａｖｉｆａｕｎａ、义县组中部Ｌｉａｏｘｉｏｒｎｉｓ Ａｖｉｆａｕｎａ和九佛堂组Ｃａｔｈａｙｏｒｎｉｓ－Ｃｈａｏｙａｎｇｉａ Ａｖｉｆａｕｎａ。义 县组和九佛堂组Ｌｙｃｏｐｔｅｒａ　Ｉ