Radiations and extinctions in relation to environmental change in the marine Lower Jurassic of northwest Europe

Paleobiology ◽  
1987 ◽  
Vol 13 (2) ◽  
pp. 152-168 ◽  
Author(s):  
A. Hallam

A diversity and turnover analysis has been undertaken for a number of invertebrate groups in the Liassic of northwest Europe. There is a more or less steady rise in diversity from the early Hettangian through to the Pliensbachian, followed by a marked decline into the early Toarcian, after which it tends once more to increase. Ammonites stand out from the other invertebrates as having had an exceptionally high rate of turnover, with very short species durations.Increase of neritic habitat area due to rise of sea level, and recolonization following the end-Triassic mass extinction event appear to be the promoters of diversity increase or radiation. Severe reductions of neritic habitat area with associated environmental deterioration, related either to episodic marine regressions or spreads of anoxic bottom waters, and bound up respectively with sea-level fall and rise, are seen as the prime factors responsible for increase of extinction rate. While the environmentally sensitive ammonites were affected by even minor regressions, the other, more eurytopic groups were evidently more resistant to these. The only event that warrants the term mass extinction, affecting nearly all the benthos and nekton but not the plankton, correlates precisely with the early Toarcian anoxic event. Several episodes can be recognized of migrations of organisms into Europe following extinctions.

2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Thomas A. Neubauer ◽  
Torsten Hauffe ◽  
Daniele Silvestro ◽  
Jens Schauer ◽  
Dietrich Kadolsky ◽  
...  

AbstractThe Cretaceous–Paleogene mass extinction event 66 million years ago eradicated three quarters of marine and terrestrial species globally. However, previous studies based on vertebrates suggest that freshwater biota were much less affected. Here we assemble a time series of European freshwater gastropod species occurrences and inferred extinction rates covering the past 200 million years. We find that extinction rates increased by more than one order of magnitude during the Cretaceous–Paleogene mass extinction, which resulted in the extinction of 92.5% of all species. The extinction phase lasted 5.4 million years and was followed by a recovery period of 6.9 million years. However, present extinction rates in European freshwater gastropods are three orders of magnitude higher than even these revised estimates for the Cretaceous–Paleogene mass extinction. Our results indicate that, unless substantial conservation effort is directed to freshwater ecosystems, the present extinction crisis will have a severe impact to freshwater biota for millions of years to come.


2016 ◽  
Vol 113 (18) ◽  
pp. 5036-5040 ◽  
Author(s):  
Manabu Sakamoto ◽  
Michael J. Benton ◽  
Chris Venditti

Whether dinosaurs were in a long-term decline or whether they were reigning strong right up to their final disappearance at the Cretaceous–Paleogene (K-Pg) mass extinction event 66 Mya has been debated for decades with no clear resolution. The dispute has continued unresolved because of a lack of statistical rigor and appropriate evolutionary framework. Here, for the first time to our knowledge, we apply a Bayesian phylogenetic approach to model the evolutionary dynamics of speciation and extinction through time in Mesozoic dinosaurs, properly taking account of previously ignored statistical violations. We find overwhelming support for a long-term decline across all dinosaurs and within all three dinosaurian subclades (Ornithischia, Sauropodomorpha, and Theropoda), where speciation rate slowed down through time and was ultimately exceeded by extinction rate tens of millions of years before the K-Pg boundary. The only exceptions to this general pattern are the morphologically specialized herbivores, the Hadrosauriformes and Ceratopsidae, which show rapid species proliferations throughout the Late Cretaceous instead. Our results highlight that, despite some heterogeneity in speciation dynamics, dinosaurs showed a marked reduction in their ability to replace extinct species with new ones, making them vulnerable to extinction and unable to respond quickly to and recover from the final catastrophic event.


2019 ◽  
Author(s):  
Mariel Ferrari ◽  
Crispin TS Little ◽  
Jed W Atkinson

As part of a study to evaluate the recovery from the early Toarcian extinction event in the Cleveland Basin, 477 new gastropod specimens were collected from mid-late Toarcian rocks of the Ravenscar section, North Yorkshire, UK. The gastropods were preserved in two modes: 1) specimens preserved with recrystallized shells, mainly in the Whitby Mudstone Formation, but also some in the Blea Wyke Sandstone Formation; 2) specimens preserved as external moulds in mineralized patches of shells in the Yellow Sandstone Member. The fossil assemblage comprised fifteen species, of which three are new: Katosira? bicarinata sp. nov., Turritelloidea stepheni sp. nov. and Striactaenonina elegans sp. nov. Four species are described in open nomenclature, as Tricarilda? sp. Jurilda sp., Cylindrobullina sp. and Cossmannina sp. The other species have previously been described: Coelodiscus minutus (Schübler in Zieten), Procerithium quadrilineatum (Römer), Pseudokatosira undulata (Benz in von Zieten), Palaeorissoina aff. acuminata (Gründel), Pietteia unicarinata (Hudleston), Globularia cf. canina (Hudleston), Striactaeonina cf. richterorum Schulbert & Nützel, Striactaenonina aff. tenuistriata (Hudleston) and Sulcoactaeon sedgvici (Phillips). Most of these species are the earliest records of their respective genera and show palaeobiogeographical connections with contemporary gastropod associations from other regions of Europe and South America. The taxonomic composition of the late Toarcian Cleveland Basin gastropod assemblage differs substantially from the faunas of the late Pliensbachian and early Toarcian Tenuicostatum Zone, showing the strong effect of the early Toarcian mass extinction event on the marine gastropod communities in the basin. Only a few gastropod species are shared between the late Toarcian faunas and the much more diverse Aalenian gastropod faunas in the Cleveland Basin, suggesting there was a facies control on gastropod occurrences at that time. This is also a potential explanation for the taxonomic differences between the late Toarcian gastropod faunas in the Cleveland Basin and those in France, and Northern and Southern Germany.


Zootaxa ◽  
2019 ◽  
Vol 4624 (1) ◽  
pp. 147-150
Author(s):  
IVAN L. F. MAGALHAES

It is now generally accepted that we are going through a major mass extinction event that is causing biodiversity loss at alarming rates (Barnosky et al. 2011). We also know that many species remain to be formally described (e.g. Huber 2014), and concerns have been raised as to whether we will be able to document these before they go extinct (Costello et al. 2013). On one hand, the number of recognized species increases exponentially (e.g. Agnarsson et al. 2013; Sangster & Luksenburg 2015). On the other, taxonomic descriptions are becoming more complete and detailed, which is necessarily more time-consuming, leading to an overall decline in the number of species described per taxonomist (Sangster & Luksenburg 2015). In this scenario, any method or protocol that increases efficiency in taxonomic descriptions is welcome. 


2001 ◽  
Vol 20 (2) ◽  
pp. 155-168 ◽  
Author(s):  
Nigel R. Ainsworth ◽  
Ian Boomer

Abstract. A thick (c.1368 m) Upper Triassic to Lower Jurassic sedimentary sequence from exploration well L134/5-1, offshore Inner Hebrides, has yielded a rich and diverse foraminiferal and ostracod microfauna. Many of the taxa have been previously described throughout northwest Europe. Poor preservation (often due to crushing and/or overgrowth) and low numbers preclude a complete taxonomic review of this material, although changes in the faunal composition, rates of faunal turnover and palaeoenvironmental analyses are discussed. This is the first published account of ostracod and foraminiferal assemblages from the Sea of Hebrides and they indicate that the sediments (argillaceous, arenaceous and carbonates) were deposited in a shelf-marine setting with environmental fluctuations that are possibly the result of local relative sea-level changes.


2003 ◽  
Vol 1 ◽  
pp. 265-300 ◽  
Author(s):  
Jan Andsbjerg ◽  
Karen Dybkjær

A sequence stratigraphic framework is established for the Jurassic of the Danish Central Graben based primarily on petrophysical log data, core sedimentology and biostratigraphic data from about 50 wells. Regional seismic lines are used to assist in the correlation of some wells and in the construction of isochore maps. In the Lower Jurassic (Hettangian–Pliensbachian) succession, five sequences have been identified. The Middle Jurassic is subdivided into four sequences that together span the uppermost Aalenian/lowermost Bajocian to the Callovian. In the Upper Jurassic, better well coverage permits greater stratigraphic resolution, and 11 sequences are identified and mapped. On the basis of the sequence stratigraphic correlation and the construction of isochore maps for individual sequences, the Jurassic basin history of the Danish Central Graben can be subdivided into seven discrete phases: (1) Shallow marine and offshore sediments deposited in a prerift basin extending from the North Sea to the Fennoscandian Border Zone (Hettangian–Pliensbachian). (2) Uplift and erosion in association with a Toarcian–Aalenian North Sea doming event. A major hiatus represents this phase in the study area. (3) Terrestrial and marginal marine sedimentation during initial rifting (latest Aalenian/earliest Bajocian – Late Callovian). (4) Early Oxfordian – Early Kimmeridgian transgression during and after a rift pulse. The sedimentary environment changed from coastal plain and marginal marine to fully marine. (5) Regression associated with a cessation or slowing of subsidence during a structural rearrangement that took place in the Late Kimmeridgian during a break in the main rift climax. Shallow to marginal marine sandstones were deposited above an erosion surface of regional extent. (6) Deep-water mudstones deposited in a composite graben with high subsidence rates related to rift pulses (latest Late Kimmeridgian – middle Middle Volgian). (7) Deposition of organic-rich mudstones and turbidite sandstones during the late Middle Volgian – Early Ryazanian. The main basin shallowed, became more symmetrical and experienced a decreasing rate of subsidence, recording the onset of the post-rift stage. A relative sea-level curve is constructed for the Middle–Late Jurassic. It shows close similarity to published eustatic (global) and relative (North Atlantic area) sea-level curves in the latest Bathonian – late Early Kimmeridgian, but differs in the Late Kimmeridgian – Middle Volgian interval, probably due to the high rate of subsidence in the study area.


2019 ◽  
Author(s):  
Mariel Ferrari ◽  
Crispin TS Little ◽  
Jed W Atkinson

As part of a study to evaluate the recovery from the early Toarcian extinction event in the Cleveland Basin, 477 new gastropod specimens were collected from mid-late Toarcian rocks of the Ravenscar section, North Yorkshire, UK. The gastropods were preserved in two modes: 1) specimens preserved with recrystallized shells, mainly in the Whitby Mudstone Formation, but also some in the Blea Wyke Sandstone Formation; 2) specimens preserved as external moulds in mineralized patches of shells in the Yellow Sandstone Member. The fossil assemblage comprised fifteen species, of which three are new: Katosira? bicarinata sp. nov., Turritelloidea stepheni sp. nov. and Striactaenonina elegans sp. nov. Four species are described in open nomenclature, as Tricarilda? sp. Jurilda sp., Cylindrobullina sp. and Cossmannina sp. The other species have previously been described: Coelodiscus minutus (Schübler in Zieten), Procerithium quadrilineatum (Römer), Pseudokatosira undulata (Benz in von Zieten), Palaeorissoina aff. acuminata (Gründel), Pietteia unicarinata (Hudleston), Globularia cf. canina (Hudleston), Striactaeonina cf. richterorum Schulbert & Nützel, Striactaenonina aff. tenuistriata (Hudleston) and Sulcoactaeon sedgvici (Phillips). Most of these species are the earliest records of their respective genera and show palaeobiogeographical connections with contemporary gastropod associations from other regions of Europe and South America. The taxonomic composition of the late Toarcian Cleveland Basin gastropod assemblage differs substantially from the faunas of the late Pliensbachian and early Toarcian Tenuicostatum Zone, showing the strong effect of the early Toarcian mass extinction event on the marine gastropod communities in the basin. Only a few gastropod species are shared between the late Toarcian faunas and the much more diverse Aalenian gastropod faunas in the Cleveland Basin, suggesting there was a facies control on gastropod occurrences at that time. This is also a potential explanation for the taxonomic differences between the late Toarcian gastropod faunas in the Cleveland Basin and those in France, and Northern and Southern Germany.


Paleobiology ◽  
1977 ◽  
Vol 3 (1) ◽  
pp. 58-73 ◽  
Author(s):  
A. Hallam

An analysis of the geographic and stratigraphic distribution of nearly 200 Jurassic bivalve genera leads to a number of new discoveries. Similarities between regions reached a maximum in the middle of the period, while the percentage of endemism correspondingly decreased. Diversity increased through the Lower Jurassic to a level which remained more or less stable from Middle Jurassic times onwards, while the origination rate shows the opposite trend. Extinction rate increased early in the period to a maximum in the Pliensbachian and fell thereafter to a low value until the Tithonian, which is marked by a sharp rise. The overall taxonomic composition of the fauna in terms of orders remained substantially stable throughout the period. The relationship with facies is discussed and three major ecological groups distinguished: marginal marine (euryhaline), shallow neritic and deep neritic. Certain pterioids have a very wide distribution and the order as a whole has a significantly higher proportion of cosmopolitan to endemic genera than any other order; the hippuritoids and trigonioids have the highest proportion of endemics. Five faunal provinces are distinguished, and the dominant control on distribution considered to be sea level. Times of high sea level were marked by widespread distribution of taxa and low endemism. High extinction rates were provoked both by regression (in the Tithonian) and by a sharp rise of sea level in the Toarcian, marked by the widespread onset of anaerobic or near-anaerobic conditions in many epicontinental seas. Some latitudinal control is recognised, notably for the hippuritoids and other stenotopic thick-shelled genera, which are confined to low latitudes.


1975 ◽  
Vol 26 ◽  
pp. 395-407
Author(s):  
S. Henriksen

The first question to be answered, in seeking coordinate systems for geodynamics, is: what is geodynamics? The answer is, of course, that geodynamics is that part of geophysics which is concerned with movements of the Earth, as opposed to geostatics which is the physics of the stationary Earth. But as far as we know, there is no stationary Earth – epur sic monere. So geodynamics is actually coextensive with geophysics, and coordinate systems suitable for the one should be suitable for the other. At the present time, there are not many coordinate systems, if any, that can be identified with a static Earth. Certainly the only coordinate of aeronomic (atmospheric) interest is the height, and this is usually either as geodynamic height or as pressure. In oceanology, the most important coordinate is depth, and this, like heights in the atmosphere, is expressed as metric depth from mean sea level, as geodynamic depth, or as pressure. Only for the earth do we find “static” systems in use, ana even here there is real question as to whether the systems are dynamic or static. So it would seem that our answer to the question, of what kind, of coordinate systems are we seeking, must be that we are looking for the same systems as are used in geophysics, and these systems are dynamic in nature already – that is, their definition involvestime.


2019 ◽  
Author(s):  
Ekaterina Larina ◽  
◽  
David J. Bottjer ◽  
Frank A. Corsetti ◽  
William M. Berelson ◽  
...  

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