Were Phanerozoic mass extinctions among brachiopod superfamilies selective by taxa longevity?

All mass extinctions are characterized by certain kind of selectivity. An analysis of stratigraphic ranges of 112 brachiopod superfamilies implies that some Phanerozoic mass extinctions (Late Ordovician, Frasnian/Famennian and Devonian/Carboniferous, Early Jurassic, and Cretaceous/Paleogene) were selective by taxa longevity. They preferentially affected relatively old superfamilies and favoured a survival of relatively young superfamilies. No explanation of this selectivity as an apparent phenomenon is fully satisfactory. The Permian/Triassic mass extinction did not favour a survival of “young” superfamilies because of abnormally low rate of origination established since the Pennsylvanian and the absence of these “young” taxa. This study confirms tentatively a difference between Paleozoic and post-Paleozoic times by the importance of post-extinction recovery intervals for taxa longevity.     

Evolutionary and biogeographical shifts in response to the Late Ordovician mass extinction

The Late Ordovician mass extinction was an interval of high extinction with inferred low ecological selectivity, resulting in little change in community structure after the event. In contrast, the mass extinction may have fundamentally changed evolutionary dynamics in the surviving groups. We investigated the phylogenetic relationships among strophomenoid brachiopods, a diverse brachiopod superfamily that was a primary component of Ordovician ecosystems. Four Ordovician families/subfamilies sampled in the analysis (Rafinesquinidae, Strophomeninae, Glyptomenidae and Furcitellinae) were reconstructed as monophyletic groups, and the base of the strophomenoid clade that dominated the Silurian recovery was reconstructed as diversifying alongside these families during the Middle Ordovician. We time‐calibrated the phylogeny and used geographical occurrences to investigate biogeographical changes in the strophomenoids through time with the R package BiogeoBEARS . Our results indicate that extinction was higher in taxa whose ranges were constrained to tropical or subtropical regions. Furthermore, our results suggest important shifts in the diversification patterns of these brachiopods after the mass extinction. While most of the strophomenoid families survived the Late Ordovician event, ecologically abundant taxonomic groups during the Ordovician were either driven to extinction, reduced in diversity, or slowly died off during the Silurian. The new abundant strophomenoid taxa derived from one clade (consisting of Silurian–Devonian groups such as Douvillinidae, Strophodontidae and Amphistrophiidae) that diversified during the post‐extinction radiation. Our results suggest the selective diversification during the Silurian radiation, rather than selective extinction in the Late Ordovician, had a greater impact on the evolutionary history of strophomenoid brachiopods.     

Intraspecific variability in rhynchonellid brachiopods: test of a competition hypothesis

The variability in the plicae of the central fold of eight rhynchonellid brachiopods – Lepidocyclus capax (Ordovician), Stegerhynchus whitii (Silurian), Megalopterorhynchus baldwini (Devonian), 'Camarotoechia' purduei (Mississippian), Wellerella osagensis (Pennsylvanian), Leiorhynchus weeksi (Permian), 'Pugnoides'; Iriassicus (Triassic) and Tetrarhynchia sp. (Jurassic) – is inversely related to the diversity of brachiopods within the faunal assemblage. Explanations for the phenotypic variability due to taxonomic splitting, sexual polymorphism or ontogenetic development are precluded or unsupported by the morphologic analysis, although a small percentage of the morphologic variability can be ascribed to ecophenotypic differentiation by environmental stimuli.
After considerations of the abiotic influences of time, geographic location and isolation, and environmental stability and homogeneity, most of the morphologic variability in these brachiopods is attributed to the biotic influence, namely competition. Other proposed relationships, i.e. population abundance, sample size, shell size or ribbing pattern and intraspecific variability are not statistically significant.     

Evolutionary rates of the Triassic marine macrofauna and sea-level changes: Evidences from the Northwestern Caucasus,Northern Neotethys (Russia)

A diverse Triassic marine macrofauna from the Northwestern Caucasus sheds new light on the biotic evolution after the end-Permian mass extinction. In the early Mesozoic, the study area was located on the northern margin of the Neotethys Ocean. Data on stratigraphic ranges of 130 genera of brachiopods, bivalves, ammonoids, corals, and sponges have been used to calculate the changes in two evolutionary rates, namely faunal transformation rate (FTR) and rate of transformation of the taxonomic diversity structure (TTDSR). The FTR demonstrates the changes in the generic composition of assemblages through geologic time, whereas the TTDSR indicates changes in the generic control of the species diversity. The Triassic marine macrofauna of the Northwestern Caucasus was characterized by very high FTR and TTDSR during the Early Triassic through early Late Triassic. The FTR slowed in the Middle Triassic, and accelerated again in the Carnian–Norian. In contrast, the FTR was abnormally slow in the Norian–Rhaetian. A remarkable turnover among macrofauna occurred at the Carnian–Norian transition. Regional sea-level changes were similar to the global eustatic fluctuations. It is difficult to establish their direct connections with changes in the evolutionary rates, although the turnover at the Carnian–Norian boundary coincided with a prominent regressive episode. In general, high evolutionary rates reported for the Triassic marine macrofauna of the Northwestern Caucasus may be explained as a consequence of the devastating end-Permian mass extinction.     

Large extinctions of articulate brachiopods in the paleozoic and their ecological and evolutionary consequences

The largest Paleozoic extinctions of articulate brachiopods occurred at the Frasnian—Famennian boundary in the Late Devonian and at the Permian—Triassic boundary. Both extinctions affected taxa of all levels, including orders, but differed in scale, course, and ecological and evolutionary consequences. The Frasnian—Famennian extinction event was selective and evolutionary activity after the crisis varied in different orders. However, in the Early Carboniferous, the brachiopod diversity was mostly restored in comparison with the Devonian maximum. In particular groups, preadaptation played a role in changes in diversity and reconstruction of communities. The brachiopod composition at this boundary changed sharply. The extinction event at the end of Permian was global and accompanied by changes in the biota. Later, in the Meso-Cenozoic, the brachiopod diversity was not restored, and bivalves acquired primary importance in various bottom communities of different sea zones where Paleozoic brachiopods previously dominated. Extinction of brachiopods at this boundary was long and gradual. The symptoms of the ecological crisis in the development of Permian brachiopods are recognized beginning from the Roadian Age, which was probably the onset of this crisis.     

Composition and dynamics of the great Phanerozoic Evolutionary Floras

Factor analysis of a data set representing the global distribution of vascular plant families through time shows the broad pattern of vegetation history can be explained in terms of five Evolutionary Floras. The Rhyniophytic (=Eotrachyophytic) Flora represents the very earliest (Silurian and earliest Devonian) vascular plants, notably the Rhyniophytopsida. The Eophytic Flora represents the early (Early–Middle Devonian) mainly homosporous land plants, notably the Zosterophyllopsida, Trimerophytopsida and early Lycopsida. The Palaeophytic Flora represents the Late Devonian and Carboniferous vegetation, which saw the introduction of heterospory among the spore producing plants and of early gymnosperms. The Mesophytic Flora first appeared in the Late Carboniferous and Permian macrofossil record, although there is palynological evidence of these plants having grown earlier in extra‐basinal habitats and was dominated by gymnosperms with more modern affinities. The Cenophytic Flora that first appeared during Cretaceous times was overwhelmingly dominated by angiosperms. The end‐Devonian, end‐Triassic and end‐Cretaceous mass‐extinction events recognized in the marine fossil record had little impact on the diversity dynamics of these Evolutionary Floras. Rather, the changes between floras mainly reflect key evolutionary innovations such as heterospory, ovules and angiospermy.     

Predation in the Ordovician and Silurian of Baltica

Signs of predation appear in the Middle Ordovician of Baltica. Shell repair dominates over the predatory borings in the Ordovician and Silurian. Predators attacked molluscs, brachiopods and tentaculitoids in the Ordovician and molluscs, tentaculitoids, brachiopods and ostracods in the Silurian. There is an increase in the number of prey species in the Late Ordovician, which could be related to the Great Ordovician Biodiversification Event. Molluscs are the favourite prey taxon in the Ordovician, but in the Silurian, molluscs became less dominant as the prey. This is probably not an artefact of preservation as Ordovician and Silurian molluscs are equally well preserved.     

Palaeozoic oolitic ironstones on the North American Craton

More than 40 mostly minor Palaeozoic oolitic ironstones (OI) accumulated on low-latitude cratonic North America, almost entirely in USA. A few Middle Cambrian OI, among the oldest anywhere, were deposited on the western cratonic shelf of USA. Widely scattered Late Cambrian ones developed on the southwestern, southeastern and northeastern flanks of the Transcontinental Arch. Middle Ordovician OI were deposited on the cratonic interior and on the southern and southeastern cratonic margins. In latest Ordovician time Neda OI spread across north-central USA east of the Arch and south of the Laurentian upland. Minor ones developed in the southern part of the Taconian foreland basin after major orogeny. Early and Middle Silurian Clinton OI flourished throughout the foreland basin in eastern USA, producing the largest OI deposit on the North American craton. Minor early Late Silurian OI accumulated in the central part of the basin. Middle and Late Devonian OI in the Acadian foreland basin in northeastern cratonic USA developed progressively westward of the encroaching Catskill delta. An isolated Middle Devonian one accumulated in southwestern cratonic USA, and latest Devonian ones in north-central USA east of the Arch.

During this Palaeozoic episode sites of OI deposition shifted eastward across the craton. Most of the OI were deposited during a hiatus in normal sedimentation, accumulating in the upper part of shoaling-upward sequences. Some early Palaeozoic ones occur in glauconitic siliciclastic-carbonate facies and contain mostly spherical hematitic ooids. These suggest derivation from iron-rich soils developed on glauconitic deposits. OI in wholly siliciclastic facies, containing distorted chamositic ooids with cores of mud peloids, were common in later Palaeozoic time. These OI, like many other Phanerozoic ones, suggest a synsedimentary to early diagenetic origin.     

Conodontophorid biodiversification during the Ordovician in South China

Wu, R., Stouge, S. & Wang, Z. 2012: Conodontophorid biodiversification during the Ordovician in South China. Lethaia, Vol. 45, pp. 432–442. Analysis of the Ordovician conodontophorid diversity pattern for South China using normalized and total diversity measures reveals that diversity peaks occurred in the mid‐Tremadocian, mid‐late Floian, early Dapingian and mid‐Darriwilian periods. The conodontophorids radiated during the Floian, maintaining relatively high diversity into the early part of the Middle Ordovician until a significant diversity decrease occurred in the late Dapingian. A relatively low diversity level prevailed in the Late Ordovician. Three diversification intervals based on origination, extinction and turnover rates have been identified i.e. (1) Tremadocian to mid‐late Floian, (2) early Dapingian and (3) late Dapingian to early Darriwilian. Diversity curves for conodontophorids, brachiopods, graptolites, acritarchs and trilobites from South China are comparable during the Early Ordovician, although differences are apparent in the Middle and Late Ordovician. In South China, conodontophorid diversity reacted primarily to sea‐level changes during the Early and Middle Ordovician, when the peak of this biodiversification generally coincided with a transgression. Climate changes – especially the global cooling that occurred during the Late Ordovician glaciation – and sea‐water chemistry were also important controlling factors. □Biodiversification, conodonts, Ordovician, South China.     

Palaeoecology and diversity of endosymbionts in Palaeozoic marine invertebrates: Trace fossil evidence

Endosymbionts are organisms that live within the growing skeleton of a live host organism, producing a cavity called a bioclaustration. The endosymbiont lives inside the bioclaustration, which it forms by locally inhibiting the normal skeletal growth of the host, a behaviour given the new ethological category, impedichnia. As trace fossils, bioclaustrations are direct evidence of past symbioses and are first recognized from the Late Ordovician (Caradoc). Bioclaustrations have a wide geographic distribution and occur in various skeletal marine invertebrates, including tabulate and rugose corals, calcareous sponges, bryozoans, brachiopods, and crinoids. Ten bioclaustration ichnogenera are recognized and occur preferentially in particular host taxa, suggesting host-specificity among Palaeozoic endosymbionts. The diversity of bioclaustrations increased during the Silurian and reached a climax by the late Middle Devonian (Givetian). A collapse in bioclaustration diversity and abundance during the Late Devonian is most significant among endosymbionts of host coral and calcareous sponge taxa that were in decline leading up to the Frasnian-Famennian mass extinction.     

Tetrapod Footprint Biostratigraphy and Biochronology

Tetrapod footprints have a fossil record in rocks of Devonian-Neogene age. Three principal factors limit their use in biostratigraphy and biochronology (palichnostratigraphy): invalid ichnotaxa based on extramorphological variants, slow apparent evolutionary turnover rates and facies restrictions. The ichnotaxonomy of tetrapod footprints has generally been oversplit, largely due to a failure to appreciate extramorphological variation. Thus, many tetrapod footprint ichnogenera and most ichnospecies are useless phantom taxa that confound biostratigraphic correlation and biochronological subdivision. Tracks rarely allow identification of a genus or species known from the body fossil record. Indeed, almost all tetrapod footprint ichnogenera are equivalent to a family or a higher taxon (order, superorder, etc.) based on body fossils. This means that ichnogenera necessarily have much longer temporal ranges and therefore slower apparent evolutionary turnover rates than do body fossil genera. Because of this, footprints cannot provide as refined a subdivision of geological time as do body fossils. The tetrapod footprint record is much more facies controlled than the tetrapod body fossil record. The relatively narrow facies window for track preservation, and the fact that tracks are almost never transported, redeposited or reworked, limits the facies that can be correlated with any track-based biostratigraphy.

A Devonian-Neogene global biochronology based on tetrapod footprints generally resolves geologic time about 20 to 50 percent as well as does the tetrapod body fossil record. The following globally recognizable time intervals can be based on the track record: (1) Late Devonian; (2) Mississippian; (3) Early-Middle Pennsylvanian; (4) Late Pennsylvanian; (5) Early Permian; (6) Late Permian; (7) Early-Middle Triassic; (8) late Middle Triassic; (9) Late Triassic; (10) Early Jurassic; (11) Middle-Late Jurassic; (12) Early Cretaceous; (13) Late Cretaceous; (14) Paleogene; (15) Neogene. Tetrapod footprints are most valuable in establishing biostratigraphic datum points, and this is their primary value to understanding the stratigraphic (temporal) dimension of tetrapod evolution.     

Earliest Triassic microbialites in the South China block and other areas: controls on their growth and distribution

Earliest Triassic microbialites (ETMs) and inorganic carbonate crystal fans formed after the end-Permian mass extinction (ca. 251.4 Ma) within the basal Triassic Hindeodus parvus conodont zone. ETMs are distinguished from rarer, and more regional, subsequent Triassic microbialites. Large differences in ETMs between northern and southern areas of the South China block suggest geographic provinces, and ETMs are most abundant throughout the equatorial Tethys Ocean with further geographic variation. ETMs occur in shallow-marine shelves in a superanoxic stratified ocean and form the only widespread Phanerozoic microbialites with structures similar to those of the Cambro-Ordovician, and briefly after the latest Ordovician, Late Silurian and Late Devonian extinctions. ETMs disappeared long before the mid-Triassic biotic recovery, but it is not clear why, if they are interpreted as disaster taxa. In general, ETM occurrence suggests that microbially mediated calcification occurred where upwelled carbonate-rich anoxic waters mixed with warm aerated surface waters, forming regional dysoxia, so that extreme carbonate supersaturation and dysoxic conditions were both required for their growth. Long-term oceanic and atmospheric changes may have contributed to a trigger for ETM formation. In equatorial western Pangea, the earliest microbialites are late Early Triassic, but it is possible that ETMs could exist in western Pangea, if well-preserved earliest Triassic facies are discovered in future work.     

Permian–Triassic Osteichthyes (bony fishes): diversity dynamics and body size evolution

The Permian and Triassic were key time intervals in the history of life on Earth. Both periods are marked by a series of biotic crises including the most catastrophic of such events, the end‐Permian mass extinction, which eventually led to a major turnover from typical Palaeozoic faunas and floras to those that are emblematic for the Mesozoic and Cenozoic. Here we review patterns in Permian–Triassic bony fishes, a group whose evolutionary dynamics are understudied. Based on data from primary literature, we analyse changes in their taxonomic diversity and body size (as a proxy for trophic position) and explore their response to Permian–Triassic events. Diversity and body size are investigated separately for different groups of Osteichthyes (Dipnoi, Actinistia, ‘Palaeopterygii’, ‘Subholostei’, Holostei, Teleosteomorpha), within the marine and freshwater realms and on a global scale (total diversity) as well as across palaeolatitudinal belts. Diversity is also measured for different palaeogeographical provinces. Our results suggest a general trend from low osteichthyan diversity in the Permian to higher levels in the Triassic. Diversity dynamics in the Permian are marked by a decline in freshwater taxa during the Cisuralian. An extinction event during the end‐Guadalupian crisis is not evident from our data, but ‘palaeopterygians’ experienced a significant body size increase across the Guadalupian–Lopingian boundary and these fishes upheld their position as large, top predators from the Late Permian to the Late Triassic. Elevated turnover rates are documented at the Permian–Triassic boundary, and two distinct diversification events are noted in the wake of this biotic crisis, a first one during the Early Triassic (dipnoans, actinistians, ‘palaeopterygians’, ‘subholosteans’) and a second one during the Middle Triassic (‘subholosteans’, neopterygians). The origination of new, small taxa predominantly among these groups during the Middle Triassic event caused a significant reduction in osteichthyan body size. Neopterygii, the clade that encompasses the vast majority of extant fishes, underwent another diversification phase in the Late Triassic. The Triassic radiation of Osteichthyes, predominantly of Actinopterygii, which only occurred after severe extinctions among Chondrichthyes during the Middle–Late Permian, resulted in a profound change within global fish communities, from chondrichthyan‐rich faunas of the Permo‐Carboniferous to typical Mesozoic and Cenozoic associations dominated by actinopterygians. This turnover was not sudden but followed a stepwise pattern, with leaps during extinction events.     

Brachiopod shell thickness links environment and evolution

While it is well established that the shapes and sizes of shells are strongly phylogenetically controlled, little is known about the phylogenetic constraints on shell thickness. Yet, shell thickness is likely to be sensitive to environmental fluctuations and has the potential to illuminate environmental perturbations through deep time. Here we systematically quantify the thickness of the anterior brachiopod shell which protects the filtration chamber and is thus considered functionally homologous across higher taxa of brachiopods. Our data come from 66 genera and 10 different orders and shows well-defined upper and lower boundaries of anterior shell thickness. For Ordovician and Silurian brachiopods we find significant order-level differences and a trend of increasing shell thickness with water depth. Modern (Cenozoic) brachiopods, by comparison, fall into the lower half of observed shell thicknesses. Among Ordovician–Silurian brachiopods, older stocks commonly have thicker shells, and thick-shelled taxa contributed more prominently to the Great Ordovician Biodiversification but suffered more severely during the Late Ordovician Mass Extinction. Our data highlight a significant reduction in maximum and minimum shell thickness following the Late Ordovician mass extinction. This points towards stronger selection pressure for energy-efficient shell secretion during times of crisis.     

Did the Late Ordovician mass extinction event trigger the earliest evolution of ‘strophodontoid’ brachiopods?

‘Strophodontoid’ brachiopods represented the majority of strophomenide brachiopods in the Silurian and Devonian periods. They are characterized by denticles developed along the hinge line. The evolution of denticles correlated with the disappearance of dental plates and teeth and were already present when the clade originated in the Late Ordovician. Specimens of Eostropheodonta parvicostellata from the Kuanyinchiao Bed (early–middle Hirnantian, uppermost Ordovician) in the Hetaoba Section, Meitan, Guizhou Province, South China, display clear fossil population variation, during a process of loss of dental plates and the development of denticles. Three phenotypes of E. parvicostellata are recognized in a single fossil bed, likely heralding a speciation process. Non-metric multidimensional scaling (NMDS) based on five key characters of genera of the Family Leptostrophiidae shows a much wider morphospace for Silurian genera than for those in the Devonian. Phylogenetic analysis of the Family Leptostrophiidae supports the NMDS analysis and mostly tracks their geological history. The fossil population differentiation in E. parvicostellata discovered between the two phases of the Late Ordovician mass extinction event (LOME) linked to a major glaciation, suggests a Hirnantian origination of the ‘strophodontoid’ morphology, and links microevolutionary change to a macroevolutionary event.     

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.     

Paleobiogeography of Mesozoic brachiopod faunas from Andean–Patagonian areas in a global context

During the Mesozoic, the Andean region has played a hinging role between high- and low-latitude faunas, which are, respectively, characterized by stocks that display long-term fidelity. This paper is aimed at providing an updated review of Late Triassic to Late Cretaceous South American articulated brachiopods in the light of previous knowledge at worldwide scale. Late Triassic brachiopods from the Argentine–Chilean Andes show unmistakable Maorian (or Notal) faunal elements alongside some more cosmopolitan genera, with certain influence of Eastern Pacific taxa. By Early Jurassic times, differentiation of Tethyan and Boreal Realms became progressively evident in Europe. In South America, Hettangian–Sinemurian brachiopod faunules from the Argentinian Andes are somewhat impoverished, with mostly cosmopolitan genera showing certain affinities to Maorian species, and with the addition of some endemics later. Increasingly, diverse Pliensbachian Andean brachiopods denote close relationships to Celto-Swabian taxa, then by Domerian times, a certain degree of endemism was developed, though somewhat delayed Tethyan influences, and persistent links with New Zealand are subordinately recognizable, too; most Toarcian assemblages reveal basically Celto-Swabian and Iberian affinities as well. East-west austral links across the Pacific may have been favored by migratory routes fringing the Gondwana margin, whereas faunal exchange with the western end of the Tethys appears to reflect an intermittent shallow-marine connection through the Hispanic Corridor. During the Middle Jurassic, distinction of Tethyan and Boreal Realms was maintained in the northern Hemisphere, and the differentiation of an Ethiopian or Southern Tethyan fauna became better characterized. Aalenian and Bajocian brachiopods of the Andes display generic affinities mainly with those from western Europe, with some minor endemic developments; brachiopods recorded from the Bathonian–Callovian of Argentina (and Chile) also occur along the northern Tethyan margin, yet with some genera extending into Indo-Ethiopian areas. During the Late Jurassic, Boreal faunas from high-latitudes became even more strongly differentiated from low-latitude, Tethyan ones. Oxfordian and Tithonian brachiopods from the Andes apparently belong to genera of cosmopolitan or northern Tethyan affiliation, yet there are few elements in common with other eastern Pacific areas, such as Mexico. Early Cretaceous brachiopods, in addition to Andean basins of Chile and western Argentina, are known also from Patagonia and Tierra del Fuego. They belong mostly to widely distributed, mainly Tethyan genera, with some quasi-cosmopolitan and circum-Pacific components (some shared with Antarctica become noticeable). Late Cretaceous brachiopods from northern Patagonia show significant affinities to Maastrichtian ones of northwest Europe and central Asia, which calls for further assessing the potential role that may have played the trans-Saharan passageway in such dispersal. Broad aspects of Mesozoic brachiopod paleobiogeography are fairly well understood, yet details of ranking and naming of certain units are still in need of more agreement.     

日本志留纪至三叠纪牙形刺生物地层

本文系统地回顾了日本志留纪至三叠纪牙形刺研究的历史和现在的成果。志留纪牙形刺只有少数零星的报道,没有建立化石带;早泥盆世已建立了５个牙形刺组合,没有中、晚泥盆世的记录;石炭纪有８个牙形刺带,其中晚石炭世３个牙形刺带;二叠纪５个牙形刺带或动物群,其中,中、晚二叠世各１个带（动物群）;三叠纪可划分出１４个牙形刺带。     

Studies of fossil brachiopods of Mongolia: Ordovician,Silurian, Devonian,Carboniferous, and Permian

Fossil brachiopods from the Ordovician, Silurian, Devonian, Carboniferous, and Permian deposits of Mongolia have been studied for the last forty-five years by the Joint Soviet-Mongolian (later RussianMongolian) Paleontological and Geological Expeditions. New data on the taxonomic composition, stratigraphic and geographic distribution of the brachiopod assemblages have been obtained. The brachiopod systematics has been further refined and detailed, and the stratigraphic and correlation scales and biogeographic reconstructions have been elaborated for the Paleozoic of Mongolia.     

Open-marine Hallstatt Limestones reworked in the Jurassic Zlatar Mélange (SW Serbia): a contribution to understanding the orogenic evolution of the Inner Dinarides

Varied west-transported and far-traveled Jurassic mélanges in southwestern Serbia represent a key to understand the geodynamic history and to solve paleogeographic questions and reconstructions in the Triassic–Jurassic passive and active margin arrangement of the Inner Dinarides. Of special interest are the carbonate-clastic radiolaritic mélange areas in the Zlatar Mountain below the Dinaridic Ophiolite nappe. The present study reports from a Middle Jurassic sedimentary mélange in the area of Vodena Poljana. Carbonate components and blocks of the mass-flow deposits consist exclusively of a reworked Middle/Late Anisian to Early Jurassic distal shelf succession. Ophiolite components from the Dinaridic Ophiolite nappe stack are missing in the spectrum. The underlying series of the Zlatar Mélange belong to Early/Middle Anisian shallow-water carbonates and to Late Anisian to Middle Jurassic deep-water sedimentary rocks of the Hallstatt facies zone. South of Vodena Poljana in the overlying ophiolitic mélange occur Late Triassic radiolaritic components from the sedimentary cover of the Late Triassic ocean floor, beside ophiolite clasts and limestone components from the continental slope. A comparison with preserved Hallstatt Limestone successions and Jurassic mélange complexes from the Eastern Alps, Western Carpathians, and Albanides strengthen the interpretation of a provenance of the Zlatar mélange from the distal passive margin facing the Neotethys Ocean to the east. An autochthonous Dinaridic Ocean west of the Drina-Ivanjica Unit cannot be confirmed.