Jurassic mountain building and Mesozoic-Cenozoic geodynamic evolution of the Northern Calcareous Alps as proven in the Berchtesgaden Alps (Germany)

New data from the Berchtesgaden Alps result in a reconstruction of the Mesozoic-Cenozoic geodynamic history of the Northern Calcareous Alps. The closure of the western part of the Neotethys Ocean started in the late Early Jurassic and is evidenced by the onset of thick clay-rich sediments in the outer shelf area (=Hallstatt realm). The Middle to early Late Jurassic contraction is documented by the migration of trench-like basins formed in front of a propagating thrust belt. Due to ophiolite obduction, these basins propagated from the outer shelf area, forming there the Bajocian to Oxfordian Hallstatt Mélange, to the Hauptdolomit/Dachstein platform area, where the Oxfordian Rofan and Tauglboden Mélanges were formed. The basins were separated by nappe fronts forming structural highs. This scenario mirrors syn-orogenic erosion and deposition in an evolving thrust belt. Active basin formation and nappe thrusting ended around the Oxfordian/Kimmeridgian boundary, which was followed by the onset of carbonate platforms on structural highs prograding towards the former basins in latest Oxfordian to Early Tithonian time. Underfilled basins remained between the platforms. Rapid deepening around the Early/Late Tithonian boundary was induced by extension due to mountain uplift and resulted in the reconfiguration of the platforms and basins related to normal and probably strike-slip faults. Erosion of the uplifted nappe stack including obducted ophiolites caused final drowning and demise of the platforms in the Berriasian. The remaining Early Cretaceous basins were filled up with molasse sediments including siliciclastics until Aptian. Around the Early/Late Cretaceous boundary again extension and strike-slip movements started, followed by Eocene thrusting and Miocene strike-slip movements with block rotations. These younger tectonic movements destroyed the Triassic to Early Cretaceous palaeogeography and arranged the modern block configuration. The described Jurassic to Early Cretaceous history corresponds with that of the Western Carpathians, the Dinarides, and the Albanides, where (1) age dating of the metamorphic soles prove late Early to Middle Jurassic inneroceanic thrusting followed by late Middle to early Late Jurassic ophiolite obduction, (2) Kimmeridgian to Tithonian shallow-water platforms formed on top of the obducted ophiolites, and (3) latest Jurassic to Early Cretaceous sediments show postorogenic character. Therefore, we correlate the Jurassic geodynamic evolution of the Northern Calcareous Alps with the closure of the western part of the Neotethys Ocean.     

Middle to Late Jurassic radiolarians from Sicily (Italy)

Middle and Upper Jurassic radiolarian faunas from two sections of Sicily are compared with the previously proposed zonations. The ages of the faunas are estimated by correlation with these zonations and by concurrent range zone. The faunas could be assigned to the Bathonian or earlier late Tithonian or early Berriasian. Two new spumellarian species (Bernoullius furcospinus andBernoullius rectispinus) from Middle Jurassic are described.     

Testing the effect of the rock record on diversity: a multidisciplinary approach to elucidating the generic richness of sauropodomorph dinosaurs through time

The accurate reconstruction of palaeobiodiversity patterns is central to a detailed understanding of the macroevolutionary history of a group of organisms. However, there is increasing evidence that diversity patterns observed directly from the fossil record are strongly influenced by fluctuations in the quality of our sampling of the rock record; thus, any patterns we see may reflect sampling biases, rather than genuine biological signals. Previous dinosaur diversity studies have suggested that fluctuations in sauropodomorph palaeobiodiversity reflect genuine biological signals, in comparison to theropods and ornithischians whose diversity seems to be largely controlled by the rock record. Most previous diversity analyses that have attempted to take into account the effects of sampling biases have used only a single method or proxy: here we use a number of techniques in order to elucidate diversity. A global database of all known sauropodomorph body fossil occurrences (2024) was constructed. A taxic diversity curve for all valid sauropodomorph genera was extracted from this database and compared statistically with several sampling proxies (rock outcrop area and dinosaur‐bearing formations and collections), each of which captures a different aspect of fossil record sampling. Phylogenetic diversity estimates, residuals and sample‐based rarefaction (including the first attempt to capture ‘cryptic’ diversity in dinosaurs) were implemented to investigate further the effects of sampling. After ‘removal’ of biases, sauropodomorph diversity appears to be genuinely high in the Norian, Pliensbachian–Toarcian, Bathonian–Callovian and Kimmeridgian–Tithonian (with a small peak in the Aptian), whereas low diversity levels are recorded for the Oxfordian and Berriasian–Barremian, with the Jurassic/Cretaceous boundary seemingly representing a real diversity trough. Observed diversity in the remaining Triassic–Jurassic stages appears to be largely driven by sampling effort. Late Cretaceous diversity is difficult to elucidate and it is possible that this interval remains relatively under‐sampled. Despite its distortion by sampling biases, much of sauropodomorph palaeobiodiversity can be interpreted as a reflection of genuine biological signals, and fluctuations in sea level may account for some of these diversity patterns.     

‘Fish’ (Actinopterygii and Elasmobranchii) diversification patterns through deep time

Actinopterygii (ray‐finned fishes) and Elasmobranchii (sharks, skates and rays) represent more than half of today's vertebrate taxic diversity (approximately 33000 species) and form the largest component of vertebrate diversity in extant aquatic ecosystems. Yet, patterns of ‘fish’ evolutionary history remain insufficiently understood and previous studies generally treated each group independently mainly because of their contrasting fossil record composition and corresponding sampling strategies. Because direct reading of palaeodiversity curves is affected by several biases affecting the fossil record, analytical approaches are needed to correct for these biases. In this review, we propose a comprehensive analysis based on comparison of large data sets related to competing phylogenies (including all Recent and fossil taxa) and the fossil record for both groups during the Mesozoic–Cainozoic interval. This approach provides information on the ‘fish’ fossil record quality and on the corrected ‘fish’ deep‐time phylogenetic palaeodiversity signals, with special emphasis on diversification events. Because taxonomic information is preserved after analytical treatment, identified palaeodiversity events are considered both quantitatively and qualitatively and put within corresponding palaeoenvironmental and biological settings. Results indicate a better fossil record quality for elasmobranchs due to their microfossil‐like fossil distribution and their very low diversity in freshwater systems, whereas freshwater actinopterygians are diverse in this realm with lower preservation potential. Several important diversification events are identified at familial and generic levels for elasmobranchs, and marine and freshwater actinopterygians, namely in the Early–Middle Jurassic (elasmobranchs), Late Jurassic (actinopterygians), Early Cretaceous (elasmobranchs, freshwater actinopterygians), Cenomanian (all groups) and the Paleocene–Eocene interval (all groups), the latter two representing the two most exceptional radiations among vertebrates. For each of these events along with the Cretaceous‐Paleogene extinction, we provide an in‐depth review of the taxa involved and factors that may have influenced the diversity patterns observed. Among these, palaeotemperatures, sea‐levels, ocean circulation and productivity as well as continent fragmentation and environment heterogeneity (reef environments) are parameters that largely impacted on ‘fish’ evolutionary history, along with other biotic constraints.     

Faunal turnover of marine tetrapods during the Jurassic–Cretaceous transition

Marine and terrestrial animals show a mosaic of lineage extinctions and diversifications during the Jurassic–Cretaceous transition. However, despite its potential importance in shaping animal evolution, few palaeontological studies have focussed on this interval and the possible climate and biotic drivers of its faunal turnover. In consequence evolutionary patterns in most groups are poorly understood. We use a new, large morphological dataset to examine patterns of lineage diversity and disparity (variety of form) in the marine tetrapod clade Plesiosauria, and compare these patterns with those of other organisms. Although seven plesiosaurian lineages have been hypothesised as crossing the Jurassic–Cretaceous boundary, our most parsimonious topology suggests the number was only three. The robust recovery of a novel group including most Cretaceous plesiosauroids (Xenopsaria, new clade) is instrumental in this result. Substantial plesiosaurian turnover occurred during the Jurassic–Cretaceous boundary interval, including the loss of substantial pliosaurid, and cryptoclidid diversity and disparity, followed by the radiation of Xenopsaria during the Early Cretaceous. Possible physical drivers of this turnover include climatic fluctuations that influenced oceanic productivity and diversity: Late Jurassic climates were characterised by widespread global monsoonal conditions and increased nutrient flux into the opening Atlantic‐Tethys, resulting in eutrophication and a highly productive, but taxonomically depauperate, plankton. Latest Jurassic and Early Cretaceous climates were more arid, resulting in oligotrophic ocean conditions and high taxonomic diversity of radiolarians, calcareous nannoplankton and possibly ammonoids. However, the observation of discordant extinction patterns in other marine tetrapod groups such as ichthyosaurs and marine crocodylomorphs suggests that clade‐specific factors may have been more important than overarching extrinsic drivers of faunal turnover during the Jurassic–Cretaceous boundary interval.     

First description of axymyiid fossils (Insecta: Diptera: Axymyiidae)

Two species of fossil insects from the Daohugou Formation of Chifeng City in Nei Monggol Autonomous Region, northeastern China are described, and recognized as Psocites pectinatus (Hong, 1983) nov. emend., nov. transl. and P. fossilis nov. sp. They are the oldest representatives of the family Callovian or Axymyiidae, and first described of this family in the Mesozoic. Although early the age of the fly-bearing beds is controversial, it is probably Oxfordian or Kimmeridgian (Late Jurassic) rather than Early Cretaceous or Middle Jurassic.     

Critical events in the evolutionary history of calcareous Nannoplankton

Calcareous nannofossil diversity, and rates of speciation and extinction are calculated for five million year intervals from their first appearance in the Late Triassic through to the Present Day. Important evolutionary events are as follows: first appearance in the Late Triassic, Triassic‐Jurassic boundary extinctions, Tithonian radiation (and the first occurrence of nannofossil carbonates), Late Cretaceous diversity maximum, Cretaceous‐Tertiary boundary extinctions, Palaeocene radiation, mid Eocene to Oligocene diversity decline, and early Miocene diversity rise. These events are related to possible causal factors of which climate appears to be the most fundamental. Other factors may include biogeographical isolation, sea level change, and the configuration of Mesozoic oceans.     

Diversity variation and tempo-spatial distributions of the Dipteridaceae ferns in the Mesozoic of China

The extant family Dipteridaceae is a remarkable leptosporangiate fern because it includes only one genus with a restricted distribution to tropical regions. The fossil record of this family has been widely reported from the Mesozoic strata in Eurasia, America, Australia, and Greenland. In China, numerous fossils of the Dipteridaceae have been documented, in total, about 74 species of 6 genera. Geographically, they are distributed both in the Southern and Northern Floristic Provinces, and were particularly well developed in the Southern Floristic Province during the Late Triassic and the Early Jurassic intervals. Fossil diversity of Dipteridaceae varies in the different episodes of the Mesozoic in China. It is shown that Dipteridaceae has undergone a diversity development process and a distinct turnover during the Mesozoic. They appear to have diversified in the warm and humid Late Triassic–Early Jurassic, but declined sharply as aridity developed in the Middle Jurassic, and became extinct at the end of the Early Cretaceous. The diversity variation and tempo-spatial distribution pattern is suggested to be linked with paleoclimatic variations during the Mesozoic.     

Lowermost occurrence of ostracod Cypridea species in East Asia and implications for the non-marine Jurassic/Cretaceous boundary

Cypridea Bosquet, 1852 is a non-marine ostracod genus of the Superfamily Cypridoidea, and the extinct Family Cyprideidae, which achieved high diversity in the Early Cretaceous. This genus plays an important role in the subdivision and correlation of strata, as well as in paleogeographic and paleoclimatic studies. Cypridea species are remarkably abundant and diverse, and are extensively distributed across East Asia. However, the lowermost occurrence of Cypridea species (LOOC) in East Asia is still being debated, varying from the Upper Jurassic to Lower Cretaceous. Here, we aim to conduct a preliminary investigation of the Cypridea-bearing strata of East Asia (China, Mongolia, Korea and Japan), and attempt to update the strata correlation, based on new progress of the ostracod correlations, as well as the progress of other research methods on the relative Jurassic/Cretaceous (J/K) strata of these areas. Results show that the LOOCs in most basins of East Asia are documented in Lower Cretaceous (～Berriasian) strata. However, Cypridea species are extremely rare near the J/K boundary interval but flourish until Valanginian–Hauterivian in most basins of East Asia. Therefore, we propose that the LOOC in each corresponding basin of East Asia can be used as an auxiliary marker of the non-marine J/K boundary. Cypridea species may have travelled first from Africa (Kimmeridgian) to Europe (J/K period), and then East Asia (Early Cretaceous), which resulted in the LOOC in East Asia later than in the other continents.     

Evolution of Lycopodiaceae (Lycopsida): estimating divergence times from rbcL gene sequences by use of nonparametric rate smoothing

By use of nonparametric rate smoothing and nucleotide sequences of the rbcL gene, divergence times in Lycopodiaceae are estimated. The results show that much extant species diversity in Lycopodiaceae stems from relatively recent cladogenic events. These results corroborate previous ideas based on paleobotanical and biogeographical data. Previous molecular phylogenetic analyses recognized a split into neotropical and paleotropical clades in Huperzia, which contains 85-90% of all living species. Connecting this biogeographical pattern with continent movements, the diversification of this epiphytic group was suggested to coincide with that of angiosperms in the mid to Late Cretaceous. Results presented here are consistent with this idea, and the diversification of the two clades is resolved as Late Cretacous (78 and 95 Myr). In the related genera Lycopodium and Lycopodiella, the patterns are somewhat different. Here species diversity is scattered among different subgeneric groups. Most of the high-diversity subgeneric groups seem to have diversified very recently (Late Tertiary), whereas the cladogenic events leading to these groups are much older (Early to Late Cretaceous). Our analysis shows that, although much living species diversity stems from relatively recent cladogenesis, the origins of the family (Early Carboniferous) and generic crown groups (Early Permian to Early Jurassic) are much more ancient events.     

Tithonian-Berriasian foraminiferal faunas from the Torinosu-type calcareous blocks of the southern Kanto Mountains, Japan: their implications for post-accretionary tectonics of Jurassic to Cretaceous terranes

The Torinosu-type limestones, having many lithologic characters showing their original deposition on shallow shelves, are widely distributed in the Jurassic to Cretaceous terranes of Japan. The foraminiferal faunas from the Jurassic to the lowermost Cretaceous of Japan were first revealed in the calcareous blocks of the southern Kanto Mountains. Distinguished microfaunas consist of 39 species including many marker species of the Upper Jurassic to Lower Cretaceous in Europe, West Asia, and North Africa such as Melathrokerion spirialis, Charentia evoluta, Freixialina planispiralis, Nautiloculina oolithica, Everticyclammina cf. virguliana, Haplophragmium lutzei and Pseudocyclammina lituus. These faunas suggest a Tithonian to Berriasian age of Torinosu-type limestones. They are contained in four tectonostratigraphic units (Kamiyozawa, Hikawa and Gozenyama Formations; Ogouchi Group) continuously accreted from Middle Jurassic to Late Cretaceous. The younger deposition age of Torinosu-type limestones than the accretion age (Bajocian to Bathonian) in the Kamiyozawa Formation and their older age than the accretion age of the Ogouchi Group (late Albian to middle Maastrichtian) are important to date the post-accretionary tectonics of Jurassic to Cretaceous terranes of Japan and to explain the emplacement process of Torinosu-type limestones.     

Diversity variation and tempo-spatial distribution of Otozamites (Bennettitales) in the Mesozoic of China

Otozamites is a representative fossil leaf morphogenus of the extinct Bennettitales, with an extensive distribution during the Mesozoic, especially in China. Understanding the fossil diversity variation and distribution pattern of Otozamites in China will provide information on biodiversity of bennettitalean plants as well as for reconstruction of palaeogeography and palaeoclimate conditions during the Mesozoic. So far, 46 species of this genus have been described in China, excluding unspecified species. The results show that the fossils of Otozamites are extensively recorded in the Late Triassic, and then reach their maximum development in the Early Jurassic, followed by a reduction in diversity in the Middle and Late Jurassic, and finally become extinct at the end of Early Cretaceous. Geographically, they occur in both Northern and Southern Floristic Provinces in the Mesozoic of China, with a relatively higher abundance in the Southern Floristic Province. It implies that the diversity variation and distribution of Otozamites are closely related to the change of the palaeoclimatic conditions. The warm and humid climate prevailed in the Late Triassic and Early Jurassic in South China, propitious to the development of Otozamites. After the Middle Jurassic, dry and hot climate may have caused the lower diversity level and blocked the development of Otozamites; finally at the end of the Early Cretaceous, the frequent arid climate may be a major cause for the extinction of Otozamites.     

Mesozoic Radiolaria of Bosnia and Serbia: New data

Jurassic and Cretaceous radiolarian faunas were discovered in bedded chert of the Dinaric and Vardar tectonic zones of Bosnia and Herzegovina. Only Triassic radiolarians have previously been described in Bosnia and Herzegovina, while the finds of Bajocian, Bathonian-Callovian, Oxfordian-Kimmeridgian, Tithonian-Berriasian, and Campanian are new. Additional localities of Triassic and Jurassic radiolarians were investigated in Serbia. By correlation with radiolarians from the previous studies within Serbia, the Late Aalenian-Bajocian and Bathonian-Callovian Serbian radiolarian beds are newly dated. The first find of Cretaceous radiolarians in Serbia is reported. The oldest Mesozoic Radiolaria-bearing formations outcropping in the Western Belt of the Vardar Zone are dated Mid-Upper Triassic. The youngest radiolarians come from the Upper Cretaceous (Campanian) of the northern part of this belt of the Vardar Zone, where they co-occur with planktonic foraminifers. The distribution of 70 radiolarian samples within sections is shown. The taxonomic composition of 39 samples is analyzed. Radiolarian species extracted from 13 samples are described and figured. The list of 72 taxa and 3 plates of Jurassic radiolarians of Bosnia and Herzegovina, 3 plates of Triassic, 1 plate of Middle Jurassic, and 1 plate of Upper Cretaceous radiolarians of Serbia are presented.     

Provenance analysis of Cenozoic conglomerates: Insights from Lower Cretaceous radiolarians in chert clasts from the Xigaze area,southern Tibet

Conglomerates, exposed on either side of the Yarlung Tsangpo suture zone (YTSZ) in southern Tibet, have attracted wide attention in elucidating uplift and erosion histories of the Himalayan-Tibetan orogen. However, the provenance of these conglomerates remains controversial. Although radiolarian-bearing chert clasts within these conglomerates have received little focus, identification of the radiolarian assemblages they contain could shed light on the provenance of these sedimentary units. We present the first report of Upper Jurassic to Lower Cretaceous (upper Kimmeridgian–lower Barremian) radiolarian assemblages recovered from chert clasts within the Liuqu and Gangrinboche conglomerates in the Xigaze area. To extract radiolarian fossils from independent clasts in the conglomerates, a detailed and efficient experimental process is illustrated. The assemblages are well correlated to those in the YTSZ and Tethyan Himalaya, showing typical Tethyan characteristics. The lithology of chert clasts and ages of constituent radiolarian faunas suggest that the chert clasts in Liuqu and Gangrinboche conglomerates were derived from the Bainang terrane. This interpretation implies that Early Cretaceous accretionary complexes in the YTSZ had been exposed and eroded before deposited as clasts in the Cenozoic Liuqu and Gangrinboche conglomerates.     

A diverse Upper Jurassic dinosaur ichnofauna from central‐west Portugal

Mateus, O. & Milàn, J. 2009: A diverse Upper Jurassic dinosaur ichnofauna from central‐west Portugal. Lethaia, Vol. 43, pp. 245–257. A newly discovered dinosaur track‐assemblage from the Upper Jurassic Lourinhã Formation (Lusitanian Basin, central‐west Portugal), comprises medium‐ to large‐sized sauropod tracks with well‐preserved impressions of soft tissue anatomy, stegosaur tracks and tracks from medium‐ to large‐sized theropods. The 400‐m‐thick Lourinhã Formation consists of mostly aluvial sediments, deposited during the early rifting of the Atlantic Ocean in the Kimmeridgian and Tithonian. The stratigraphic succession shows several shifts between flood‐plain mud and fluvial sands that favour preservation and fossilization of tracks. The studied track‐assemblage is found preserved as natural casts on the underside of a thin bivalve‐rich carbonate bed near the Tithonian–Kimmeridgian boundary. The diversity of the tracks from the new track assemblage is compared with similar faunas from the Upper Jurassic of Asturias, Spain and the Middle Jurassic Yorkshire Coast of England. The Portuguese record of Upper Jurassic dinosaur body fossils show close similarity to the track fauna from the Lourinhã Formation. □Dinosaur tracks, Lusitanian Basin, Portugal, skin impressions, Upper Jurassic.     

The oldest turtle from Portugal corresponding to the only pre-Kimmeridgian plesiochelyid (basal Eucryptodira) recognized at the generic level

A shell coming from an upper Oxfordian section of the Lusitanian Basin located in Alqueidão da Serra (Municipality of Porto de Mós, West Central Portugal) is here presented. It corresponds to the oldest remain of a turtle identified in Portugal. In fact, the record of Jurassic turtles identified in pre-Kimmeridgian levels of Europe is very scarce. The new specimen represents the second worldwide identification of a Plesiochelyid turtle (basal Eucryptodira) performed in pre-Kimmeridgian levels, being the only one recognized at generic level. Therefore, this specimen corresponds to the oldest identification of Craspedochelys, a genus well-represented in Kimmeridgian and Tithonian levels of several European countries. This finding contributes the first evidence on the synchronous coexistence of more than a member of Plesiochelyidae in pre-Kimmeridgian levels, which provides arguments to justify the relatively wide diversity known for this exclusively Jurassic clade during the Kimmeridgian and the Tithonian.     

Pleurotomaria DeFrance, 1826 (Gastropoda,Mollusca) from the Lower Bajocian (Middle Jurassic) sediments of Luxembourg,with considerations on its systematics,evolution and palaeobiogeographical history

Abstract: Pleurotomaria species from lower Bajocian (Middle Jurassic) sediments of south‐western Luxembourg housed in the National Natural History Museum of Luxembourg are described. Seven species are recognized, one of which is new, Pleurotomaria faberi sp. nov. A more detailed definition of the diagnostic characters of the genus is proposed and the morphological continuity between Talantodiscus and Pleurotomaria is demonstrated, suggesting that the former cannot be considered as a distinct taxon. The palaeoecology, evolution and palaeobiogeographical history of Pleurotomaria are outlined. Pleurotomaria presumably first appeared in late Middle Triassic of New Zealand where it underwent a relative diversification up to the Hettangian (Early Jurassic). From early Hettangian, most of its evolutionary history took place in Europe and western Tethys. In the European epicontinental seas, Pleurotomaria experienced two important radiations. The first occurred in the Early Jurassic, with a peak in the late Pliensbachian, and was marked by an expansion of the distribution to the central part of western Tethys. After a collapse in species diversity, probably related to the early Toarcian anoxic event, a second radiation occurred. This culminated in the early Bajocian and was mainly confined in a region encompassing southern England, Paris Basin and southern Germany. Low‐spired species, formerly attributed to Talantodiscus, probably originated independently and iteratively during the history of Pleurotomaria. The facies and associated benthic faunas suggest that Pleurotomaria probably lived on shallow soft bottoms composed of mixed calcareous–siliciclastic sediments. The two main Early Jurassic and early Middle Jurassic radiations of the genus took place in these environments. Records of the genus in Jurassic carbonate platform deposits are very few and concern mainly post‐Bajocian species.     

Taxic and morphological diversification during the early radiation of Clupeomorpha (Actinopterygii,Teleostei)

Evolutionary radiation is a problematic concept whose definition and classification have recently changed. Radiations can be defined as the pattern of abrupt increase in diversity of a lineage. It is relevant to evaluate the presence and interaction of different types of radiation in extant and fossil organisms to adequately delimitate the radiation types and to know the diversity in the context of Earth's history. Here, we employed the superorder Clupeomorpha at the Early–Late Cretaceous boundary as a study case to investigate radiation types and their interactions, using both taxic and morphological approaches. Clupeomorpha is an extensively studied, diverse and ancient teleostean superorder with wide geographical and ecological distributions. We propose a model for calculating rates of origination in order to analyse the taxic diversification and employ geometric morphometrics to analyse the morphological diversification that occurred at the temporal boundary. The results suggest the absence of taxic radiation due to a constant increase in taxon origination. However, the expansion of the phylomorphospace occupation and the disparity increase suggest the presence of a ‘climatic–geographical’ or ‘broad diversification-like’ disparity, according to current classifications. This illustrates the incompatibility of current radiation classifications with this case study.     

<Emphasis Type="Italic">Milax vitukhini</Emphasis>, a new radiolarian species from the Upper Jurassic of the Ust’-Belaya Mountains of the Koryak Upland

A new species, Milax vitukhini sp. nov., from the newly recognized Kimmeridgian–Tithonian radiolarian association from volcanogenic–siliceous–terrigenous rocks of the Borozda Creek Basin (Ust’-Belsky Mountains, Koryak Upland) is described.     

Embryonic shell structure of Early–Middle Jurassic belemnites,and its significance for belemnite expansion and diversification in the Jurassic

Early Jurassic belemnites are of particular interest to the study of the evolution of skeletal morphology in Lower Carboniferous to the uppermost Cretaceous belemnoids, because they signal the beginning of a global Jurassic–Cretaceous expansion and diversification of belemnitids. We investigated potentially relevant, to this evolutionary pattern, shell features of Sinemurian–Bajocian Nannobelus, Parapassaloteuthis, Holcobelus and Pachybelemnopsis from the Paris Basin. Our analysis of morphological, ultrastructural and chemical traits of the earliest ontogenetic stages of the shell suggests that modified embryonic shell structure of Early–Middle Jurassic belemnites was a factor in their expansion and colonization of the pelagic zone and resulted in remarkable diversification of belemnites. Innovative traits of the embryonic shell of Sinemurian–Bajocian belemnites include: (1) an inorganic–organic primordial rostrum encapsulating the protoconch and the phragmocone, its non‐biomineralized component, possibly chitin, is herein detected for the first time; (2) an organic rich closing membrane which was under formation. It was yet perforated and possessed a foramen; and (3) an organic rich pro‐ostracum earlier documented in an embryonic shell of Pliensbachian Passaloteuthis. The inorganic–organic primordial rostrum tightly coating the protoconch and phragmocone supposedly enhanced protection, without increase in shell weight, of the Early Jurassic belemnites against explosion in deep‐water environment. This may have increased the depth and temperature ranges of hatching eggs, accelerated the adaptation of hatchlings to a nektonic mode of life and promoted increasing diversity of belemnoids. This study supports the hypothesis that belemnite hatchlings were ‘a miniature of the adults’.