scholarly journals Current extinction rate in European freshwater gastropods greatly exceeds that of the late Cretaceous mass extinction

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.


2015 ◽  
Vol 42 (5) ◽  
pp. 19-26
Author(s):  
Horacio de la Cueva Salcedo

Environmental changes happen all the time. Changing environments bring about selection of organisms, and there is no organism that does not modify its environment to make a living, survive, and reproduce. These changes are the main motors of evolution and, consequently, the main cause of biodiversity. Environmental violence—unsustainable use and extraction of natural resources—is the way capitalist economies exploit nature. The extinction rates associated with the current unsustainable use of resources are sufficient to assume that we are experiencing a sixth mass extinction event. The rate at which humans are transforming the environment leaves no time for evolutionary adaptation. We need to reduce environmental violence for life to maintain its normal processes. Without knowledge of nature and the consequences of violence against nature, we will become another of the planet’s extinct species. Los cambios ambientales ocurren todo el tiempo. Los ambientes cambiantes propician la selección de organismos y no hay organismo que no modifique su ambiente para subsistir y reproducirse. Estos cambios son los principales motores de la evolución y por lo tanto la causa principal de la biodiversidad. La violencia ambiental—el uso y la extracción insostenibles de los recursos naturales—es la manera en que las economías capitalistas explotan la naturaleza. Las tasas de extinción asociadas con el uso insostenible de los recursos son suficientes para considerar que estamos experimentando la sexta extinción masiva de especies. El ritmo al cual los seres humanos están transformando el ambiente no deja tiempo para la adaptación evolutiva. Necesitamos reducir la violencia ambiental para que la vida pueda mantener sus procesos normales. Sin el conocimiento de la naturaleza y de las consecuencias de la violencia contra ella, nos convertiremos en otra de las especies extintas de nuestro planeta.


1986 ◽  
Vol 60 (1) ◽  
pp. 107-115 ◽  
Author(s):  
Douglas S. Jones ◽  
David Nicol

Rudists arose in the Late Jurassic and survived for nearly 100 m.y. before becoming extinct at the end of the Cretaceous. Over this interval they diversified gradually during the Late Jurassic and Early Cretaceous, rapidly in the mid-Cretaceous, then more slowly in the Late Cretaceous. Total rates of origination and extinction during the Late Jurassic and Early Cretaceous were uniform and comparable to those reported for other groups. The Late Cretaceous, however, was characterized by high and widely fluctuating total origination and extinction rates. Per taxon rates reveal a similar pattern except for high and variable rates in the Jurassic. The number of genera increased from the Oxfordian to a peak in the Cenomanian, decreased in the Turonian and Coniacian coinciding with a minor mass extinction event, and rose to a zenith in the Maastrichtian. Unlike other groups investigated, the rudists were at their highest level of diversity immediately prior to their disappearance.Rudist genera survived for a mean of 12 m.y., whereas families survived for a mean of 48 m.y. Survivorship curves for generic cohorts, based upon survival of all rudist genera that evolved during each stage, exhibit a concave shape when the effects of mass extinction and variance at low diversities are considered. Causal factors involved in the final disappearance of the rudists remain unclear; however, their tropical provinciality in the Late Cretaceous contributed to their vulnerability to mass extinction.


2007 ◽  
Vol 44 (10) ◽  
pp. 1397-1411 ◽  
Author(s):  
Carmen Arias

The extinction and recovery of Ostracoda at the Pliensbachian–Toarcian (P–T) boundary are analyzed based on a database of taxonomically revised Pliensbachian to Toarcian transition ostracod assemblages. In contrast to earlier assertions, the results of this study indicate that ostracod extinction rates were significant in comparison with other marine invertebrates. An extinction rate of 54% has been calculated for upper Pliensbachian ostracod species occurring in more than one section. Diversification took place in the latest Pliensbachian (Spinatum Zone) and early Toarcian (Tenuicostatum Zone), whereas diversity decrease occurred in the middle early Toarcian (Strangewaysi Subzone, Serpentinus Zone). This notable diversity decline in the early Toarcian corresponds to a global mass extinction time, whose peak has been documented in the Tenuicostatum Zone. Meanwhile, the ostracod mass extinction occurred within the Serpentinus Zone and was followed by radiation and recovery in the succeeding Bifrons Zone. Similar diversity changes of ostracods are observed in other European areas, although in the Cordillera Ibérica, the demise began later. Many aspects of this event are still debated, and there is no common cause or single set of climatic or environmental changes common to this event. The supposed extinction-causing environmental changes resulting from anoxia episodes are unclear and are unlikely to have been of sufficient intensity or geographic extent to cause this global extinction. In this paper, the decrease in marine species diversity is explained by a new palaeoceanographic scenario, in which a rapid global cooling episode is regarded as the ultimate cause.


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.


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

2020 ◽  
Author(s):  
Marisa D. Knight ◽  
◽  
Runsheng Yin ◽  
Clara L. Meier ◽  
James V. Browning ◽  
...  

Paleobiology ◽  
1990 ◽  
Vol 16 (2) ◽  
pp. 187-203 ◽  
Author(s):  
Douglas H. Erwin

Paleozoic and post-Paleozoic marine faunas are strikingly different in composition. Paleozoic marine gastropods may be divided into archaic and modern groups based on taxonomic composition, ecological role, and morphology. Paleozoic assemblages were dominated by pleurotomariids (Eotomariidae and Phymatopleuridae), the Pseudozygopleuridae, and, to a lesser extent, the Euomphalidae, while Triassic assemblages were dominated by the Trochiina, Amberleyacea, and new groups of Loxonematoidea and Pleurotomariina. Several new groups of caenogastropods appeared as well. Yet the importance of the end-Permian mass extinction in generating these changes has been questioned. As part of a study of the diversity history of upper Paleozoic and Triassic gastropods, to test the extent to which taxonomic and morphologic trends established in the late Paleozoic are continued after the extinction, and to determine the patterns of selectivity operating during the extinction, I assembled generic and morphologic diversity data for 396 genera in 75 families from the Famennian through the Norian stages. Within this interval, gastropod genera underwent an adaptive radiation during the Visean and Namurian, largely of pleurotomariids, a subsequent period of dynamic stability through the Leonardian, a broad-based decline during the end-Permian mass extinction, and a two-phase post-extinction rebound during the Triassic. The patterns of generic diversity within superfamily-level clades were analyzed using Q-mode factor analysis and detrended correspondence analysis.The results demonstrate that taxonomic affinity, previous clade history, generic age, and gross morphology did not determine survival probability of genera during the end-Permian extinction, with the exception of the bellerophontids, nor did increasing diversity within clades or expansion of particular morphologies prior to the extinction facilitate survival during the extinction or success after it. The pleurotomariids diversified during the Lower Permian, but were heavily hit by the extinction. Similarly, trochiform and turriculate morphologies, among those which Vermeij (1987) has identified as having increased predation resistance, were expanding in the late Paleozoic, but suffered similar extinction rates to other nondiversifying clades. Survival was a consequence of broad geographic and environmental distribution, as was the case during background periods.


Geosciences ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 479
Author(s):  
Ignacio Arenillas ◽  
Vicente Gilabert ◽  
José A. Arz

After the Cretaceous/Paleogene boundary (KPB) catastrophic mass extinction event, an explosive evolutionary radiation of planktic foraminifera took place in consequence of the prompt occupation of empty niches. The rapid evolution of new species makes it possible to establish high-resolution biozonations in the lower Danian. We propose two biostratigraphic scales for low-to-middle latitudes spanning the first two million years of the Danian. The first is based on qualitative data and includes four biozones: the Guembelitria cretacea Zone (Dan1), the Parvularugoglobigerina longiapertura Zone (Dan2), the Parvularugoglobigerina eugubina Zone (Dan3), and the Parasubbotina pseudobulloides Zone (Dan4). The latter two are divided into several sub-biozones: the Parvularugoglobigerina sabina Subzone (Dan3a) and the Eoglobigerina simplicissima Subzone (Dan3b) for the Pv. eugubina Zone, and the Praemurica taurica Subzone (Dan4a), the Subbotina triloculinoides Subzone (Dan4b), and the Globanomalina compressa Subzone (Dan4c) for the P. pseudobulloides Zone. The second scale is based on quantitative data and includes three acme-zones (abundance zones): the Guembelitria Acme-zone (DanAZ1), the Parvularugoglobigerina-Palaeoglobigerina Acme-zone (DanAZ2), and the Woodringina-Chiloguembelina Acme-zone (DanAZ3). Both biozonations are based on high-resolution samplings of the most continuous sections of the lower Danian worldwide and have been calibrated with recent magnetochronological and astrochronological dating.


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