Paleoecology of the K-Pg mass extinction survivor Guembelitria (Cushman): isotopic evidence from pristine foraminifera from Brazos River, Texas (Maastrichtian)

Paleobiology ◽  
10.1666/13317 ◽  
2014 ◽  
Vol 40 (1) ◽  
pp. 24-33 ◽  
Author(s):  
Sarit Ashckenazi-Polivoda ◽  
Carmi Rak ◽  
Ahuva Almogi-Labin ◽  
Berner Zsolt ◽  
Ofer Ovadia ◽  
...  

The late Maastrichtian sediments of the Mullinax-1 and Mullinax-3 boreholes from Brazos River, Texas, offer pristine material. These cores are prime candidates for providing an extraordinary window into the ecology of Guembelitria, a key genus in the K/Pg mass extinction event, as well as information on the habitats of other neritic species. Stable oxygen and carbon isotope analyses were performed on six planktic species (Guembelitria cretacea, Globigerinelloides asper, Heterohelix globulosa, Paraspiroplecta navarroensis, Pseudoguembelina costulata, Rugoglobigerina rugosa) and three benthic genera (Gavelinella, Cibicides, and Lenticulina). Our records support the contention that Guembelitria was fully planktic, as indicated by its δ18O values, which overlap the other planktic species, despite its possible origin from a tychopelagic benthic ancestor. However, Guembelitria is distinctly ranked very low in δ13C values, which overlap the benthic records. The anomalously low δ13C values of Guembelitria may represent an isotopic disequilibrium due to fast shell growth, like in its modern analogue Gallitellia vivans. Another explanation may be that these values are attributable to a neustonic life mode in the uppermost part of the oceans, where photosynthesis is inhibited by high UV and the near absence of nutrients. Because these waters are not photosynthetically depleted, calcification using carbon directly from these waters should yield δ13C values consistent with those found in Guembelitria. The ecological strategy that Guembelitria species used to deal with the nutrient-poor surface-water environments was an opportunistic blooming during stressful times of Maastrichtian global warming events and later during the K-Pg catastrophe.

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 ◽  
...  

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.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Cory J. D. Matthews ◽  
Fred J. Longstaffe ◽  
Jack W. Lawson ◽  
Steven H. Ferguson

AbstractKiller whales (Orcinus orca) are distributed widely in all oceans, although they are most common in coastal waters of temperate and high-latitude regions. The species’ distribution has not been fully described in the northwest Atlantic (NWA), where killer whales move into seasonally ice-free waters of the eastern Canadian Arctic (ECA) and occur year-round off the coast of Newfoundland and Labrador farther south. We measured stable oxygen and carbon isotope ratios in dentine phosphate (δ18OP) and structural carbonate (δ18OSC, δ13CSC) of whole teeth and annual growth layers from killer whales that stranded in the ECA (n = 11) and NWA (n = 7). Source δ18O of marine water (δ18Omarine) at location of origin was estimated from dentine δ18OPvalues, and then compared with predicted isoscape values to assign individual distributions. Dentine δ18OPvalues were also assessed against those of other known-origin North Atlantic odontocetes for spatial reference. Most ECA and NWA killer whales had mean δ18OPand estimated δ18Omarinevalues consistent with18O-depleted, high-latitude waters north of the Gulf Stream, above which a marked decrease in baseline δ18O values occurs. Several individuals, however, had relatively high values that reflected origins in18O-enriched, low-latitude waters below this boundary. Within-tooth δ18OSCranges on the order of 1–2‰ indicated interannual variation in distribution. Different distributions inferred from oxygen isotopes suggest there is not a single killer whale population distributed across the northwest Atlantic, and corroborate dietary and morphological differences of purported ecotypes in the region.


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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