AMMONOIDS AND THE TRIASSIC/JURASSIC BOUNDARY IN THE HIMALAYAS OF SOUTHERN TIBET

Abstract:  The sections of Germig in the Nyalam area, southern Tibet, provide a continuous exposure of ammonoid-bearing, uppermost Triassic and basal Jurassic strata. Eighteen species (three of them new) are described and illustrated: Choristoceras marshi Hauer , C. aff. marshi, C. cf. nobile Mojsisovics , C. nyalamense sp. nov., Eopsiloceras germigense sp. nov. , Pleuroacanthites aff. biformis (Sowerby) , Rhacophyllites sp., Nevadaphyllites cf. psilomorphus (Neumayr), Neophyllites sp. indet., Neophyllites cf. biptychus (Lange), Psiloceras tibeticum sp. nov., P. calliphyllum (Neumayr), Euphyllites cf. struckmanni (Neumayr), Discamphiceras pleuronotum (Canavari), Alsatites spp., Kammerkarites frigga , and K. sp. The ammonoid fauna shows a strong affinity to that of the Northern Calcareous Alps, although diversity in the Calliphyllum Zone is markedly lower. The ammonoid succession across the Triassic/Jurassic boundary is subdivided into four zones: the Rhaetian Marshi, the basal Hettangian Tibeticum, the lower Hettangian Calliphyllum, and the middle Hettangian Pleuronotum zones. It is the only known succession across the Triassic/Jurassic boundary in the Tethyan Realm that is not condensed. The Marshi and Calliphyllum zones are correlated with the same zones in the Northern Calcareous Alps. The Tibeticum Zone, a new local zone, is transitional between the Marshi and the Calliphyllum zones in that it yields both choristoceratids and psiloceratids. Its base is taken to mark the base of the Jurassic System in the eastern Tethys.     

Strontium isotope stratigraphy of the Gabbs Formation (Nevada): implications for global Norian–Rhaetian correlations and faunal turnover

The Luning and Gabbs formations in west‐central Nevada, USA represent a Late Triassic shallow marine sedimentary succession with global significance (the Gabbs Formation was a candidate for the basal Jurassic GSSP). Typically, the Norian–Rhaetian stage boundary is placed at the contact between the formations, and the Rhaetian–Hettangian boundary (the Triassic–Jurassic boundary) is within the Müller Canyon Member of the Gabbs Formation. However, the use of different biostratigraphical index‐species schemes in Norian–Rhaetian successions between Tethys and Panthalassa, the two largest ocean basins at the time, makes precise correlation problematic. Here, we compare ⁸⁷Sr/⁸⁶Sr measurements of well‐preserved carbonate shell material from Nevada to the well‐known and biostratigraphically constrained ⁸⁷Sr/⁸⁶Sr record from Tethys, where a negative excursion in ⁸⁷Sr/⁸⁶Sr is noted across the Norian–Rhaetian boundary. Our new ⁸⁷Sr/⁸⁶Sr data from the Luning and Gabbs formations reveal a comparable trend, with a sharp drop in ⁸⁷Sr/⁸⁶Sr within the Nun Mine Member of the Gabbs Formation, suggesting the position of the Norian–Rhaetian boundary is higher in the succession, and not between the Luning and Gabbs formations as previously defined. Relating the stage boundary using global isotopic signals is a useful tool for biostratigraphical correlation of successions between Tethys and Panthalassa, and for estimating the rate of faunal turnover at the Norian–Rhaetian stage boundary in comparison with the succeeding Late Triassic mass extinction. If correct, this biostratigraphical–chemostratigraphical correlation suggests that the current index groups for the Panthalassic stage boundary should be changed.     

Aspects of late triassic palynology. 3. Palynology of latest triassic and earliest jurassic deposits of the northern limestone alps in Austria and southern Germany,with special reference to a palynological characterization of the Rhaetian stage in Europe

The present paper provides a palynological analysis of samples from the “Kössener Schichten”, “Schattwalder Schichten” and the ammonoid (Psiloceras planorbe)-bearing beds of the “Fleckenmergel/Fleckenkalk” found in the vicinity of Salzburg (Austria and adjacent part of Germany).It is shown that the compositional development of latest Triassic—earliest Jurassic palynological assemblages from Alpine sequences matches the situation in the Germanic realm. A characteristic phase in this development is interpreted in terms of the Rhaetipollis germanicus Assemblage Zone. It is considered that this zone could well be regarded as a palynological characterization of the Rhaetian Stage in Europe and North America.Although palynology does not support the Rhaetian concept based on the occurrence of the species Choristoceras marshi exclusively, the traditional ammonoid-based Triassic—Jurassic boundary can be palynologically recognized.     

Facies stacking and extinctions across the Triassic–Jurassic boundary in a peritidal succession from western Sicily

An uppermost Triassic–lowermost Jurassic carbonate platform succession, which is 430 m thick, in northwestern Sicily is described with the aim to provide new data on the sedimentological and biological variations across the Triassic–Jurassic boundary in peritidal environments. The studied succession belonged to the rimmed carbonate shelf that developed during the Late Triassic along the margins of the Ionian Tethys. The peritidal sediments consist of meter-scale shallowing-upward cycles formed by subtidal, intertidal, and supratidal facies. Three main informal units are differentiated along the section on the basis of the variations recorded by the subtidal facies. The lower and middle units are attributed to the Rhaetian, on the basis of the common presence of the foraminifer Triasina hantkeni, associated with several benthic foraminifers, such as Aulotortus sinuosus and Auloconus permodiscoides. Megalodontids are particularly abundant and large in the lower unit, whereas they become rare in the middle unit and disappear in the upper unit. The last occurrence of T. hantkeni, along with the disappearance of the benthic foraminifer fauna, and the bloom of the calcareous alga Thaumatoporella parvovesiculifera is assumed as a proxy of the Rhaetian–Hettangian boundary. Recovery biota during the early Jurassic occurs about 20 m upward of the boundary zone, marked by the appearance of benthic foraminifers, such as Siphovalvulina sp. The observed biostratigraphic signature in the studied section is easily comparable to similar Tethyan sections already described from Italy, Greece, and Turkey; thus, it is believed that the faunistic turnover does not reflect local facies variations, in response to changes in the accommodation space of the platform, but regional changes in a more wide area of ocean Tethys.     

Rhaetian magneto-biostratigraphy from the Southern Alps (Italy): Constraints on Triassic chronology

New Late Triassic–earliest Jurassic magneto-biostratigraphic data have been obtained from three overlapping sections in the Southern Alps, Italy (Costa Imagna, Brumano, Italcementi Quarry), composed of ~ 520 m of shallow-marine carbonates outcropping in stratigraphic continuity. Characteristic magnetic components of presumed depositional age record a sequence of 9 normal and reverse polarity magnetozones (as defined by at least three stratigraphically superposed samples) linked by conodont and palynofloral evidence from this study and the literature to Rhaetian to Triassic–Jurassic boundary age. This represents a significantly larger number of polarity zones than previously recognized in more condensed Rhaetian sections from the literature, and by inference represents more time. These data are placed in a broader Late Triassic temporal framework by means of correlations to published magneto-biostratigraphic data from the Tethyan marine Pizzo Mondello section and the Newark astronomical polarity time scale (APTS). This framework is consistent with a position of the Norian–Rhaetian boundary (as defined at Brumano and Pizzo Mondello by the first appearance of Misikella posthernsteini) within Newark magnetozones E17r–E19r in the ~ 207–210 Ma time interval, in basic agreement with the position originally estimated in the Newark using pollen biostratigraphy (E18 at 208–209 Ma). This framework is also consistent with the position of the Triassic–Jurassic boundary interval (placed at Italcementi Quarry at the acme of Kraeuselisporites reissingeri coincident with a negative carbon isotope excursion) correlative to just above Newark magnetozone E23r and just below the oldest CAMP lavas dated at ~ 202 Ma. Hence, we estimate the duration of the Rhaetian to be ~ 5.5–8.5 Myr (or even longer if the Triassic–Jurassic boundary is instead placed above the negative carbon isotope excursion as at Kuhjoch, which is the designated GSSP for the base of the Hettangian), and encompassing 9 magnetozones. This duration contrasts with a duration of ~ 2 Myr and only ~ 4 magnetozones in several alternative published magneto-biostratigraphic schemes.     

Reduction in animal abundance and oxygen availability during and after the end-Triassic mass extinction

The end-Triassic biodiversity crisis was one of the most severe mass extinctions in the history of animal life. However, the extent to which the loss of taxonomic diversity was coupled with a reduction in organismal abundance remains to be quantified. Further, the temporal relationship between organismal abundance and local marine redox conditions is lacking in carbonate sections. To address these questions, we measured skeletal grain abundance in shallow-marine limestones by point counting 293 thin sections from four stratigraphic sections across the Triassic/Jurassic boundary in the Lombardy Basin and Apennine Platform of western Tethys. Skeletal abundance decreased abruptly across the Triassic/Jurassic boundary in all stratigraphic sections. The abundance of skeletal organisms remained low throughout the lower-middle Hettangian strata and began to rebound during the late Hettangian and early Sinemurian. A two-way ANOVA indicates that sample age (p < .01, η² = 0.30) explains more of the variation in skeletal abundance than the depositional environment or paleobathymetry (p < .01, η² = 0.15). Measured I/Ca ratios, a proxy for local shallow-marine redox conditions, show this same pattern with the lowest I/Ca ratios occurring in the early Hettangian. The close correspondence between oceanic water column oxygen levels and skeletal abundance indicates a connection between redox conditions and benthic organismal abundance across the Triassic/Jurassic boundary. These findings indicate that the end-Triassic mass extinction reduced not only the biodiversity but also the carrying capacity for skeletal organisms in early Hettangian ecosystems, adding to evidence that mass extinction of species generally leads to mass rarity among survivors.     

Refinements in the Upper Permian to Lower Jurassic stratigraphy of Karakorum, Pakistan

New sampling on critical intervals of the uppermost Permian and Triassic successions of the Northern Karakorum Terrain in the Karakorum Range (Pakistan) has refined the stratigraphy. Two types of successions may be distinguished in the Karakorum Range: a carbonate platform succession, spanning the whole interval from Upper Permian to Upper Triassic, possibly with several gaps; and a basinal succession, deposited from the Middle Permian to Early Carnian (Late Triassic), when the carbonate platform prograded into the basin. With the approaching and later docking of the Karakorum Block against the Asian margin closing the Paleo-Tethys, a portion of Karakorum emerged while another part subsided as a fore-deep, receiving clastics from the emerging Cimmerian Range. Molassic sediments filled the basin, whilst shallow-water carbonates transgressed over the emerged carbonate platform sometime between the latest Triassic and the Pliensbachian (Early Jurassic), with Cimmerian deformation occurring to the north. The age control is provided by conodonts, with assemblages of late Wuchiapingian, Changhsingian, Induan (Griesbachian and Dienerian), late Olenekian, early Anisian, late Ladinian, and early Carnian ages, respectively. Some information on the section around the P/T boundary is provided by palynology and isotopic C¹³ values. The dating of the Norian/Rhaetian platform is provided by foraminifers.     

Sea-level changes as controlling factor of early diagenesis: the reefal limestones of Adnet (Late Triassic,Northern Calcareous Alps,Austria)

The uppermost Rhaetian Adnet reef is part of the Dachstein carbonate platform and is situated at the transition to the intrashelf Kössen Basin. Its diagenetic evolution is investigated focusing on dissolution cavities in the Tropfbruch quarry of Adnet (near Salzburg) stratigraphically situated immediately below the Triassic–Jurassic boundary. Sea-level changes due to global eustatic trends and regional tectonics are assumed to be the controlling factors in the development of a manifold diagenetic sequence characterized by phases of meteoric dissolution, marine and burial cementation, and internal sedimentation. Despite small-scale variations of the sequence, a superordinate pattern of diagenetic phases could be elaborated. Small-scale eustatic sea-level falls subordinate to a global regression trend caused subaerial exposures of the Adnet reef in the latest Rhaetian to earliest Hettangian. The result was karstification and meteoric dissolution of aragonitic coral skeletons (Retiophyllia) leading to the formation of biomoldic porosity. Coral septa which escaped dissolution were transformed into neomorphic calcite spar under meteoric–phreatic conditions. A first generation of dog-tooth cements precipitated sporadically on the altered coral skeletons. Eustatic sea-level rise in Early to Mid-Hettangian times caused a renewed flooding of the pore space of the Adnet reef by marine water and the influx of a first generation of internal sediments (IS I), derived from the karstified host rock of the Upper Rhaetian reef limestone. These internal sediments are overgrown by radiaxial-fibrous calcites (RFCs) whose oxygen-isotopic signature (δ¹⁸O = ?1.3 (±0.7)‰) indicates precipitation in deeper (colder) water (18–21°C) due to a first phase of drowning. An intermediate phase of eustatic sea-level lowstand in the Late Hettangian is expressed by dissolution and corrosion of RFCs. Rapid drowning of the Dachstein carbonate platform due to eustatic sea-level rise and tectonic movements took place in the Early Sinemurian and a second generation of internal sediments (IS II) derived from the Lower Sinemurian Adnet Formation is washed into the dissolution cavities. Where IS II is absent, RFCs are overgrown by a second generation of dog-tooth cements with a bright-luminescent outer rim indicating the transition to negative redox conditions in the pore water during shallow burial. Burial diagenesis is represented by blocky calcite cements which occlude the remaining pore space. Depleted oxygen-isotope values and significant Fe contents indicate precipitation under reducing redox conditions and elevated temperatures of 30–50°C at burial depths of 420–870 m. Locally, replacive saddle dolomite is the latest diagenetic phase in the Adnet reef indicating crystallization under hydrothermal influences related to compressional subduction regimes of the Penninic Ocean.     

Biostratigraphic correlation,paleoenvironment stress,and subrosion pipe collapse: Dutch Rhaetian shales uncover their secrets

A subrosion pipe or sinkhole is a geologic phenomenon that occurs due to dissolution of strata in the subsurface causing the overlying sediments to collapse. The subrosion pipe in the Winterswijk quarry complex in the eastern Netherlands yielded rare, dark-colored shales. Bivalves and palynomorphs indicate that the shales were deposited during the Rhaetian (uppermost Triassic). In addition, detailed correlation with other NW European localities in Great Britain, Austria, and Germany further constrained the age of the shales to the middle of the Rhaetian. The shales were deposited in a near-coastal environment and contained a low diverse macroinvertebrate fauna with bivalves and some brittle stars that lived in a hostile environment, probably caused by low salinity and oxygen levels. These middle Rhaetian shales were mixed with dark-colored middle to late Hettangian sediments, both overlying Middle Triassic (Anisian) strata, which is present in the pipe as well. The presence of Rhaetian sediments in the subrosion pipe reopened the discussion on its age of formation. We suggest that a collapse in the Middle Eocene is most likely. This research expands the knowledge of the marine realms in the uppermost Triassic in Europe, just prior to the Permian–Triassic extinction event.     

Synchronous Wildfire Activity Rise and Mire Deforestation at the Triassic–Jurassic Boundary

The end-Triassic mass extinction event (∼201.4 million years ago) caused major faunal and floral turnovers in both the marine and terrestrial realms. The biotic changes have been attributed to extreme greenhouse warming across the Triassic–Jurassic (T–J) boundary caused by massive release of carbon dioxide and/or methane related to extensive volcanism in the Central Atlantic Magmatic Province (CAMP), resulting in a more humid climate with increased storminess and lightning activity. Lightning strikes are considered the primary source of wildfires, producing charcoal, microscopically recognized as inertinite macerals. The presence of polycyclic aromatic hydrocarbons (PAHs) of pyrolytic origin and allochthonous charcoal in siliciclastic T–J boundary strata has suggested widespread wildfire activity at the time. We have investigated largely autochthonous coal and coaly beds across the T–J boundary in Sweden and Denmark. These beds consist of predominantly organic material from the in situ vegetation in the mires, and as the coaly beds represent a substantial period of time they are excellent environmental archives. We document a remarkable increase in inertinite content in the coal and coaly beds across the T–J boundary. We show estimated burning temperatures derived from inertinite reflectance measurements coupled with palynological data and conclude that pre-boundary late Rhaetian mire wildfires included high-temperature crown fires, whereas latest Rhaetian–Sinemurian mire wildfires were more frequent but dominated by lower temperature surface fires. Our results suggest a major change in the mire ecosystems across the T–J boundary from forested, conifer dominated mires to mires with a predominantly herbaceous and shrubby vegetation. Contrary to the overall regional vegetation for which onset of recovery commenced in the early Hettangian, the sensitive mire ecosystem remained affected during the Hettangian and did not start to recover until around the Hettangian–Sinemurian boundary. Decreasing inertinite content through the Lower Jurassic suggests that fire activity gradually resumed to considerable lower levels.     

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.     

Permian and early Triassic isotopic records of carbon and strontium in Australia and a scenario of events about the Permian‐Triassic boundary

The negative shift in δ¹³C values of carbonate carbon at the Permian/Triassic boundary is one of the better documented geochemical signatures of a mass extinction event. The similar negative shift in δ¹³C values in organic carbon from Permian/Triassic boundary marine sediments in Austria and Canada is shown to occur also in marine and non‐marine sediments from Australian sedimentary basins. This negative shift in δ¹³C values is used to calibrate Australian sections lacking diagnostic faunal elements identifying the Permian/Triassic boundary. The minimum in the carbonate ⁸⁷Sr/⁸⁶Sr seawater curve from carbonates across the Guadalupian/Ochoan Stage boundary, mainly from North America, is shown to occur also in brachiopod calcite mainly from the Bowen Basin of eastern Australia, hence providing a second calibration point in the Australian sedimentary record. These two geochemical events support a model of a runaway greenhouse developing about the Permian/Triassic boundary; this is inferred to have contributed to the end‐Permian mass extinction.     

The Kuehneotheriidae (Mammaliaformes) from Saint-Nicolas-de-Port (Upper Triassic,France): a Systematic Review

The origin and first diversification of mammals in the Upper Triassic remain poorly understood, in part because many fossil discoveries are not fully studied, and in part because the material remains poor. The Saint-Nicolas-de-Port quarry (Rhaetian, France) is the second most important locality that yielded remains of Kuehneotherium, after the fissure-fillings of the Glamorganshire (Lower Jurassic, Wales). This study identifies one new species of Kuehneotherium, K. stanislavi, sp. nov., and a new genus of Kuehneotheriidae, Fluctuodon necmergor, gen. et sp. nov. For these two new species, lower and upper molars are described and the first reconstructions of the postcanine row are proposed. Comparisons with material of Kuehneotherium from other Upper Triassic sites (Syren in Luxembourg, Emborough in England, and Jameson Land in Greenland) suggest two distinct Upper Triassic specific kuehneotheriid assemblages, respectively, west and east of the London Brabant Massif. They also suggest that the extinction event during the Triassic/Jurassic transition did not have a great impact on Kuehneotherium.     

Microbes,mud and methane: cause and consequence of recurrent Early Jurassic anoxia following the end‐Triassic mass extinction

The end‐Triassic mass extinction (c. 201.6 Ma) was one of the five largest mass‐extinction events in the history of animal life. It was also associated with a dramatic, long‐lasting change in sedimentation style along the margins of the Tethys Ocean, from generally organic‐matter‐poor sediments during the Triassic to generally organic‐matter‐rich black shales during the Jurassic. New core material from Germany provides biomarker evidence of persistent photic‐zone euxinia during the Hettangian, the onset of which is associated with a series of both negative and positive carbon isotope excursions. Combined inorganic and organic geochemical and micropalaeontological analyses reveal strong similarities between the Hettangian and the better‐known Toarcian anoxic event. These events appear to be the most clearly expressed events within a series of anoxic episodes that also include poorly studied black shale intervals during the Sinemurian and Pliensbachian. Both the Hettangian and Toarcian events are marked by important changes in phytoplankton assemblages from chromophyte‐ to chlorophyte‐dominated assemblages within the European Epicontinental Seaway. Phytoplankton changes occurred in association with the establishment of photic‐zone euxinia, driven by a general increase in salinity stratification and warming of surface waters. For both events, the causes of large negative carbon isotope excursions remain incompletely understood; evidence exists for both variation in the δ¹³C of atmospheric CO₂ and variation in the sources of organic carbon. Regardless of the causes of δ¹³C variability, long‐term ocean anoxia during the Early Jurassic can be attributed to greenhouse warming and increased nutrient delivery to the oceans triggered by flood basalt volcanism.     

Where and when the earliest coccolithophores?

Gardin, S., Krystyn, L., Richoz, S., Bartolini, A. & Galbrun, B. 2012: Where and when the earliest coccolithophores? Lethaia, Vol. 45, pp. 507–523. New calcareous nannofossil analyses from the Northern Calcareous Alps of Austria are herein used to update and improve the state of knowledge about the oldest occurrence of coccolithophores reported in the literature. Previously reported Norian occurrences of coccoliths were based on an obsolete Triassic chronostratigraphy, in which the Rhaetian stage was subsumed into the Norian (‘Sevatian 2’). The oldest stratigraphical record of coccoliths spp. lies just below the Norian‐Rhaetian boundary and the first coccolith species, Crucirhabdus minutus, is recorded from the base of Rhaetian stage. The latter bio‐event is located just above the First Occurrence of the conodont Misikella posthersteni and the first occurrence of the ammonoid Paracochloceras suessi in the Steinbergkogel section (Austria), Global Stratotype Section and Point (GSSP) candidate for the Norian–Rhaetian boundary. The appearance of the coccolith Crucirhabdus minutus is seen as a robust biochronological datum that will provide useful constraints for Triassic biostratigraphy, palaeoclimatic modelling and phylogenetic reconstructions. The new calcareous nannofossil biochronology of Steinbergkogel that we present herein completes the existing biostratigraphic characterization of the Norian‐Rhaetian transition based on conodonts and ammonoids and strengthens the position of Steinbergkogel as the best GSSP proposed section for the base of the Rhaetian. The record of coccolithophores across the Norian–Rhaetian boundary at Steinbergkogel takes place along with a discernible increase in abundance of Prinsiosphaera triassica, as well as the appearance of Euconusphaera zlambachensis, which are the two most important Rhaetian pelagic carbonate producers. This succession of bio‐events is interpreted as the initiation of the pelagic carbonate production driven by the successful spreading of calcareous nannofossils in the Western Tethys during the Rhaetian. □Austria, Calcareous Alps, coccolithophores, Triassic.     

Holothurian faunal changes at the Triassic-Jurassic boundary

The diversity pattern of holothurian echinoderms during the late Triassic-early Jurassic is quantitatively analysed to examine the effect of different taxonomic approaches. Whereas sclerite morphospecies indicate major faunal change during the Norian with significant extinction in the Upper Norian. changes are less pronounced for parafamilies and least for biologically based groups. Perceived diversity patterns are subject to bias. including a significant effect of relative research effort on morphospecies and parafamily data. A large proportion of Lazarus taxa in the Rhaetian-Hettangian indicates a sampling problem due to preservational or geographic bias. * Holothurian. Norian, Rhaetian, Hettangian, taxonomic diversity, origination, extinction .     

Triassic/Jurassic carbonates from the Hochfelln Mountain (Northern Calcareous Alps)—its facies, silicified fauna and implications for the end-Triassic biotic crisis

A suite of Early Mesozoic (Late Triassic, Norian to Early Jurassic) calcareous beds was studied from the Hochfelln Mountain in the Northern Calcareous Alps (NCA, South Germany). The Hauptdolomit Group consists of thick peritidal deposits and is overlain by basin deposits of the Rhaetian Kössen Formation and Rhaetian reefoidal limestone with corals. Unlike many other sections in the Tethys realm, coral growth seems to continue into the Jurassic or starts again relatively early within the Early Jurassic. Silicified corals and other marine invertebrates are present in the calcareous, micritic Hochfelln Beds. A re-examination of previously collected ammonite material indicates the presence of Coroniceras sp. which suggests an Early Sinemurian age for the Hochfelln Beds. Abundant sponge spicules (spiculites) suggest that sponges were the source for the silicification. The site produced one of the most diverse Early Jurassic (Sinemurian) gastropod faunas of the NCA (25–30 species, some undescribed). The relatively diverse Early Sinemurian gastropod fauna and coral growth indicate rapid recovery from the end-Triassic biotic crisis.     

RHAETIAN (LATE TRIASSIC) MONOTIS (BIVALVIA: PECTINOIDA) FROM THE EASTERN NORTHERN CALCAREOUS ALPS (AUSTRIA) AND THE END-NORIAN CRISIS IN PELAGIC FAUNAS

Abstract:  Species of marine bivalves of the pectinoid genus Monotis provide useful biochronologic indices for the Late Triassic (middle Norian–earliest Rhaetian). We report the succession of Monotis at Hernstein in Lower Austria where typical late Norian Monotis salinaria (Schlotheim) are overlain by strata with apparently the youngest Monotis known of demonstrable Rhaetian age: Monotis hoernesi Kittl and Monotis rhaetica sp. nov., a species closely related to M. rudis Gemmellaro. A Rhaetian (Sevatian 2) age is confirmed by the co-occurrence of Monotis with the platform conodont Misikella posthernsteini and close association with the ammonoid Paracochloceras . A review of late Norian monotid species indicates that a profound extinction event occurred in the pelagic realm at or close to the Norian/Rhaetian boundary where c. 15 monotids ( Monotis s.l . and Maorimonotis ) became extinct. The surviving Monotis are dwarfed when compared to their Norian predecessors and may represent an ecological/phylogenetic response to the crisis.