2021 in paleontology: Difference between revisions
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* A study comparing the morphology of the maxillary canal of ''[[Heleosaurus]] scholtzi'', ''[[Varanosaurus]] acutrostris'', ''[[Orovenator]] mayorum'' and ''[[Prolacerta]] broomi'', and evaluating the implications of the morphology of the maxillary canal for the knowledge of the phylogenetic placement of [[Varanopidae|varanopids]], is published by Benoit ''et al.'' (2021).<ref>{{Cite journal|last1=Benoit |first1=J. |last2=Ford |first2=D. P. |last3=Miyamae |first3=J. A. |last4=Ruf |first4=I. |title=Can maxillary canal morphology inform varanopid phylogenetic affinities? |year=2021 |journal=Acta Palaeontologica Polonica |volume=66 |doi=10.4202/app.00816.2020 }}</ref> |
* A study comparing the morphology of the maxillary canal of ''[[Heleosaurus]] scholtzi'', ''[[Varanosaurus]] acutrostris'', ''[[Orovenator]] mayorum'' and ''[[Prolacerta]] broomi'', and evaluating the implications of the morphology of the maxillary canal for the knowledge of the phylogenetic placement of [[Varanopidae|varanopids]], is published by Benoit ''et al.'' (2021).<ref>{{Cite journal|last1=Benoit |first1=J. |last2=Ford |first2=D. P. |last3=Miyamae |first3=J. A. |last4=Ruf |first4=I. |title=Can maxillary canal morphology inform varanopid phylogenetic affinities? |year=2021 |journal=Acta Palaeontologica Polonica |volume=66 |doi=10.4202/app.00816.2020 }}</ref> |
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* A study on the [[paleoneurology]] and likely paleobiology of ''[[Anteosaurus]] magnificus'' is published by Benoit ''et al.'' (2021).<ref>{{Cite journal|last1=Benoit |first1=J. |last2=Kruger |first2=A. |last3=Jirah |first3=S. |last4=Fernandez |first4=V. |last5=Rubidge |first5=B. S. |title=Palaeoneurology and palaeobiology of the dinocephalian therapsid ''Anteosaurus magnificus'' |year=2021 |journal=Acta Palaeontologica Polonica |volume=66 |issue=1 |pages=29–39 |doi=10.4202/app.00800.2020 |doi-access=free }}</ref> |
* A study on the [[paleoneurology]] and likely paleobiology of ''[[Anteosaurus]] magnificus'' is published by Benoit ''et al.'' (2021).<ref>{{Cite journal|last1=Benoit |first1=J. |last2=Kruger |first2=A. |last3=Jirah |first3=S. |last4=Fernandez |first4=V. |last5=Rubidge |first5=B. S. |title=Palaeoneurology and palaeobiology of the dinocephalian therapsid ''Anteosaurus magnificus'' |year=2021 |journal=Acta Palaeontologica Polonica |volume=66 |issue=1 |pages=29–39 |doi=10.4202/app.00800.2020 |doi-access=free }}</ref> |
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* New specimen of ''[[Lanthanostegus]] mohoii'', providing new information on the anatomy of the skull of this dicynodont and providing the first direct correlation between the lower [[Abrahamskraal Formation]] at Jansenville on the eastern side of the [[Karoo Basin]] and the southwestern part of this basin, is described by Rubidge, Day & Benoit (2021).<ref>{{cite journal |last1=Rubidge |first1=B. S. |last2=Day |first2=M. O. |last3=Benoit |first3=J. |year=2021 |title=New Specimen of the Enigmatic Dicynodont ''Lanthanostegus mohoii'' (Therapsida, Anomodontia) from the Southwestern Karoo Basin of South Africa, and its Implications for Middle Permian Biostratigraphy |journal=Frontiers in Earth Science |volume=9 |pages=Article 668143 |doi=10.3389/feart.2021.668143 }}</ref> |
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* New burrow casts containing skeletons of ''[[Diictodon]]'', including associated remains of adult and infant specimens, are described by Smith ''et al.'' (2021), who consider it likely that portions of underground burrows produced ''Diictodon'' by were facultatively used as brood chambers.<ref>{{Cite journal|last1=Smith |first1=R. M. H. |last2=Angielczyk |first2=K. D. |last3=Benoit |first3=J. |last4=Fernandez |first4=V. |title=Neonate aggregation in the Permian dicynodont ''Diictodon'' (Therapsida, Anomodontia): Evidence for a reproductive function for burrows? |year=2021 |journal=Palaeogeography, Palaeoclimatology, Palaeoecology |volume=569 |pages=Article 110311 |doi=10.1016/j.palaeo.2021.110311 }}</ref> |
* New burrow casts containing skeletons of ''[[Diictodon]]'', including associated remains of adult and infant specimens, are described by Smith ''et al.'' (2021), who consider it likely that portions of underground burrows produced ''Diictodon'' by were facultatively used as brood chambers.<ref>{{Cite journal|last1=Smith |first1=R. M. H. |last2=Angielczyk |first2=K. D. |last3=Benoit |first3=J. |last4=Fernandez |first4=V. |title=Neonate aggregation in the Permian dicynodont ''Diictodon'' (Therapsida, Anomodontia): Evidence for a reproductive function for burrows? |year=2021 |journal=Palaeogeography, Palaeoclimatology, Palaeoecology |volume=569 |pages=Article 110311 |doi=10.1016/j.palaeo.2021.110311 }}</ref> |
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* Redescription and a study on the phylogenetic relationships of ''[[Kunpania]] scopulusa'' is published by Angielczyk, Liu & Yang (2021).<ref>{{Cite journal|last1=Angielczyk |first1=K. D. |last2=Liu |first2=J. |last3=Yang |first3=W. |year=2021 |title=A Redescription of ''Kunpania scopulusa'', a Bidentalian Dicynodont (Therapsida, Anomodontia) from the ?Guadalupian of Northwestern China |journal=Journal of Vertebrate Paleontology |volume=in press |pages=e1922428 |doi=10.1080/02724634.2021.1922428 }}</ref> |
* Redescription and a study on the phylogenetic relationships of ''[[Kunpania]] scopulusa'' is published by Angielczyk, Liu & Yang (2021).<ref>{{Cite journal|last1=Angielczyk |first1=K. D. |last2=Liu |first2=J. |last3=Yang |first3=W. |year=2021 |title=A Redescription of ''Kunpania scopulusa'', a Bidentalian Dicynodont (Therapsida, Anomodontia) from the ?Guadalupian of Northwestern China |journal=Journal of Vertebrate Paleontology |volume=in press |pages=e1922428 |doi=10.1080/02724634.2021.1922428 }}</ref> |
Revision as of 20:11, 2 June 2021
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Paleontology or palaeontology is the study of prehistoric life forms on Earth through the examination of plant and animal fossils.[1] This includes the study of body fossils, tracks (ichnites), burrows, cast-off parts, fossilised feces (coprolites), palynomorphs and chemical residues. Because humans have encountered fossils for millennia, paleontology has a long history both before and after becoming formalized as a science. This article records significant discoveries and events related to paleontology that occurred or were published in the year 2021.
2021 in science |
---|
Fields |
Technology |
Social sciences |
Paleontology |
Extraterrestrial environment |
Terrestrial environment |
Other/related |
Flora
Cnidarians
New taxa
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Sp. nov |
Valid |
Baron-Szabo |
A stony coral. |
|||||
Sp. nov |
Valid |
Löser in Löser et al. |
A coral belonging to the family Solenocoeniidae. |
|||||
Gen. et sp. nov |
Valid |
Guo et al. |
A hexangulaconulariid. Genus includes new species D. isofacialis. |
|||||
Gen. et sp. nov |
Valid |
Löser in Löser et al. |
Early Cretaceous (Valanginian) |
Sierra del Pozo Formation |
A coral belonging to the family Aulastraeoporidae. The type species is E. llanoensis. |
|||
Sp. nov |
Valid |
Löser in Löser et al. |
Early Cretaceous (Valanginian) |
Sierra del Pozo Formation |
A coral belonging to the family Actinastreidae. |
|||
Gen. et sp. nov |
Valid |
Kołodziej & Marian |
A colonial coral belonging to the group Pachythecaliina, possibly belonging to the superfamily Heterocoenioidea and the family Carolastraeidae. Genus includes new species M. roniewiczae. |
|||||
Gen et comb. nov |
Valid |
Song et al. |
Late Cambrian |
A member of Leptothecata belonging to the group Macrocolonia; a new genus for "Siberiograptus" simplex Lin (1985). |
||||
Gen. et sp. nov |
Valid |
Löser in Löser et al. |
A stony coral belonging to the family Rhizangiidae. The type species is S. aquilai. |
Research
- A study on the morphology, embryonic development and phylogenetic relationships of Quadrapyrgites is published by Zhao et al. (2021), who interpret this taxon and its probable relative Olivooides as more likely to be diploblastic cnidarians than triploblastic cycloneuralians.[8]
- An exceptionally preserved conulariid specimen, keeping its aperture semi-closed and making it possible to see most of the internal part of the closure with rib continuation inwards, is described from the Ordovician of southeastern Brandenburg (Germany) by Sendino & Bochmann (2021).[9]
Arthropods
Arachnids
New taxa
Name | Novelty | Status | Authors | Age | Type locality | Location | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Valid |
Wunderlich & Müller |
Cretaceous |
Possibly a member of the family Dipluridae. The type species is A. spicula. |
||||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of the family Tetrablemmidae. The type species is A. plenfemur. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of Araneomorphae belonging to the family Pholcochyroceridae. |
|||
Sp. nov |
Valid |
Khaustov et al. |
Late Eocene |
A mite belonging to the group Raphignathoidea and the family Barbutiidae. |
||||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. The type species is B. crassifemora. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the family Salticoididae. |
|||
Burmadictyna fissura[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the family Salticoididae. |
||
Burmadictyna similis[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the family Salticoididae. |
||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Araneoidea and the family Zarqaraneidae. The type species is B. trispinae. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of Araneomorphae belonging to the family Burmorsolidae. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Theridiidae. The type species is C. concavum. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the new family Crassicephalidae. The type species is C. parvibulbus. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Araneoidea and the family Zarqaraneidae. |
|||
Gen. et sp. nov |
Valid |
Lourenço in Lourenço & Velten |
Cretaceous |
Burmese amber |
A scorpion belonging to the family Protoischnuridae. The type species is C. smeelei. |
|||
Gen. et sp. nov |
Valid |
Downen & Selden |
A spider belonging to the family Palpimanidae. Genus includes new species C. vittari. |
|||||
Sp. nov |
Valid |
Khaustov et al. |
Late Eocene |
A mite belonging to the group Heterostigmata and the family Dolichocybidae. |
||||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the new family Dubiodeinopsidae. The type species is D. spinifemora. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the new family Dubiouloboridae. The type species is D. incompletus. |
|||
Gen. et 2 sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the new family Dubiouloboridae. The type species is D. praeta; genus also includes D. procerembolus. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of the family Tetrablemmidae. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider of uncertain phylogenetic placement, possibly a member of an early branch of the RTA clade. The type species is E. cretaceus. |
|||
Sp. nov |
Valid |
Khaustov et al. |
Late Eocene |
Rovno amber |
A mite belonging to the group Heterostigmata and the family Tarsocheylidae. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of Araneomorphae belonging to the family Pholcochyroceridae. The type species is K. oblonga. |
|||
Sp. nov |
Junior homonym |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of Araneomorphae belonging to the family Pholcochyroceridae. The specific name is preoccupied Longissipalpus cochlea Wunderlich (2017). |
|||
Longissipalpus impudicus[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of Araneomorphae belonging to the family Pholcochyroceridae. |
||
Gen. et sp. nov |
Valid |
Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of Araneomorphae belonging to the new family Megasetidae. The type species is M. colphepeiroides. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Palpimanoidea and the family Micropalpimanidae. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Theridiidae. The type species is M. longissispinae. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Leptonetidae. |
|||
Sp. nov |
Valid |
Selden |
A spider belonging to the group Mesothelae and to the new family Palaeothelidae. |
|||||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Mecysmaucheniidae. The type species is P. depressa. |
|||
Sp. nov |
Valid |
Khaustov et al. |
Late Eocene |
Rovno amber |
A mite belonging to the group Heterostigmata and the family Acarophenacidae. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
|||
Paramiagrammopes curvatus[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes furca[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes granulatus[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes inaequalis[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes inclinatus[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes multifemurspinae[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes paracurvatus[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes pilosus[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes pollex[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes semiapertus[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes simplex[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes sulcus[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes texter[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Paramiagrammopes unibrevispina[10] |
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Palpimanoidea and the family Planarchaeidae. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Palpimanoidea and the family Planarchaeidae. The type species is P. longicorpus. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Palpimanoidea and the family Vetiatoridae. The type species is P. circulus. |
|||
Gen. et sp. nov |
Valid |
Wriedt et al. |
Cretaceous |
A pseudoscorpion belonging to the family Chthoniidae. Genus includes new species P. burmiticus. |
||||
Sp. nov |
In press |
Magalhaes et al. |
Burmese amber |
A spider belonging to the family Psilodercidae. |
||||
Sp. nov |
Valid |
Khaustov et al. |
Late Eocene |
Rovno amber |
A mite belonging to the group Heterostigmata and the family Acarophenacidae. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Leptonetoidea and the family Protoaraneoididae. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of the family Tetrablemmidae. The type species is P. deformans. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Palpimanoidea and the family Vetiatoridae. The type species is P. fruticosus. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of Araneomorphae belonging to the family Eopsilodercidae. |
|||
Sp. nov |
Valid |
Selden |
Carboniferous (Kasimovian) |
A spider belonging to the group Mesothelae and the family Arthrolycosidae. |
||||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. The type species is P. tuberculatus. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the new family Scutuloboridae. The type species is S. admirabilis. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the new family Scutuloboridae. The type species is S. pumilio. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Deinopoidea and the new family Scutuloboridae. The type species is S. spiralembolus. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Archaeidae. The type species is S. aberrans. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the group Araneoidea and the family Zarqaraneidae. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Uloboridae. The type species is S. crux. |
|||
Sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A spider belonging to the family Telemidae, possibly a species of Telemofila. |
|||
Gen. et sp. nov |
Valid |
Wunderlich in Wunderlich & Müller |
Cretaceous |
Burmese amber |
A member of the family Tetrablemmidae. The type species is T. penicillus. |
Research
- Revision of the fossil record of whip spiders is published by Haug & Haug (2021).[18]
Crustaceans
New taxa
Malacostracans
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
In press |
Ferratges, Hyžný & Zamora |
A member of Axiidea belonging to the family Anacalliacidae. Genus includes new species A. enigma. |
|||||
Gen. et sp. nov |
In press |
Ferratges, Hyžný & Zamora |
Early Cretaceous (Aptian) |
Forcall Formation |
A member of Axiidea. Genus includes new species A. longimanus. |
|||
Gen. et sp. nov |
Valid |
Winkler |
A member of Caridea, possibly belonging to the family Palaemonidae. The type species is B. haereri. |
|||||
Sp. nov |
Valid |
Winkler |
Late Jurassic (Tithonian) |
Altmühltal Formation |
A member of Caridea. |
|||
Sp. nov |
Valid |
De Angeli & Alberti |
Eocene (Bartonian-Priabonian) |
A crab, a species of Carpilius. |
||||
Sp. nov |
In press |
Bruce et al. |
||||||
Sp. nov |
In press |
Bruce et al. |
Early Cretaceous (Aptian) |
Sierra Madre Formation |
A member of Isopoda, a species of Cirolana. |
|||
Sp. nov |
In press |
Bruce et al. |
Early Cretaceous (Aptian) |
Sierra Madre Formation |
A member of Isopoda, a species of Cirolana. |
|||
Gen. et sp. nov |
In press |
Ferratges, Hyžný & Zamora |
Early Cretaceous (Aptian) |
Forcall Formation |
A hermit crab. Genus includes new species C. josaensis. |
|||
Sp. nov |
In press |
Ferratges, Hyžný & Zamora |
Early Cretaceous (Aptian) |
Forcall Formation |
A member of Axiidea belonging to the family Callianideidae. |
|||
Gen. et sp. nov |
Valid |
Schädel et al. |
Late Cretaceous (Cenomanian) |
Burmese amber |
A member of Isopoda belonging to the group Epicaridea. The type species is C. nidis. |
|||
Sp. nov |
Valid |
Fraaije, Van Bakel & Jagt |
A hermit crab belonging to the family Schobertellidae. |
|||||
Gen. et sp. nov |
Valid |
Schädel, Hyžný & Haug |
A member of Isopoda belonging to the group Cymothoida. The type species is E. madelineae. |
|||||
Sp. nov |
Valid |
Wei et al. |
Late Neogene |
A member of Amphipoda. |
||||
Sp. nov |
Valid |
Becker, Fraaije & Mulder |
A member of the family Glypheidae. |
|||||
Sp. nov |
Valid |
Winkler |
Late Jurassic (Tithonian) |
Altmühltal Formation |
A member of Caridea. |
|||
Sp. nov |
Valid |
Feldmann et al. |
A species of Linuparus. |
|||||
Sp. nov |
In press |
Ferratges, Hyžný & Zamora |
Early Cretaceous (Aptian) |
Forcall Formation |
A member of Axiidea. |
|||
Sp. nov |
Valid |
Charbonnier et al. |
A member of the family Mecochiridae. |
|||||
Sp. nov |
Valid |
Poschmann |
A member of Phyllocarida. |
|||||
Gen. et sp. nov |
Valid |
Beschin et al. |
Late Eocene |
A hermit crab. Genus includes new species P. scaligera. |
||||
Sp. nov |
In press |
Bruce et al. |
Early Cretaceous (Aptian) |
Sierra Madre Formation |
A member of Isopoda belonging to the family Cirolanidae. |
|||
Sp. nov |
Valid |
Devillez & Charbonnier |
A member of Erymoidea. |
|||||
Gen. et sp. nov |
Valid |
Haug & Haug |
Altmühltal Group (Eichstätt Subformation) |
A mantis shrimp. The type species is T. laurae. |
Ostracods
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Sp. nov |
In press |
Vázquez García et al. |
Cretaceous (Albian–Cenomanian) |
|||||
Nom. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
|||||
Sp. nov |
In press |
Wang et al. |
Middle Eocene to Oligocene |
A species of Candona. |
||||
Sp. nov |
In press |
Kshetrimayum et al. |
A species of Candona. |
|||||
Sp. nov |
In press |
Vázquez García et al. |
Cretaceous (Albian–Cenomanian) |
Riachuelo Formation |
||||
Sp. nov |
In press |
Maia et al. |
Late Pleistocene |
|||||
Sp. nov |
In press |
Kshetrimayum et al. |
Late Cretaceous (Maastrichtian) |
|||||
Sp. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
|||||
Sp. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
|||||
Sp. nov |
In press |
Song et al. |
Late Devonian |
|||||
Sp. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
|||||
Sp. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
|||||
Sp. nov |
In press |
Vázquez García et al. |
Cretaceous (Albian–Cenomanian) |
Riachuelo Formation |
||||
Sp. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
|||||
Sp. nov |
In press |
Vázquez García et al. |
Cretaceous (Albian–Cenomanian) |
Riachuelo Formation |
||||
Sp. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
|||||
Sp. nov |
Valid |
Glinskikh & Tesakova |
||||||
Sp. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
|||||
Sp. nov |
In press |
Vázquez García et al. |
Cretaceous (Albian–Cenomanian) |
Riachuelo Formation |
||||
Sp. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
|||||
Sp. nov |
Valid |
Slipper |
Late Cretaceous (Turonian) |
Other crustaceans
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Sp. nov |
In press |
Gale |
A barnacle. |
|||||
Concinnalepas rugosa[41] |
Sp. nov |
In press |
Gale |
A barnacle. |
||||
Gen. et sp. nov |
In press |
Tang, Mychko, Feldmann & Schweitzer in Tang et al. |
A member of Cyclida. Genus includes new species M. terengganuensis. |
Research
- A study on the anatomy and phylogenetic relationships of the species "Penaeus" natator from the Santonian of Lebanon is published by Audo, Winkler & Charbonnier (2021), who interpret this species as a relative of Pseudodrobna kenngotti from the Late Jurassic of Germany, and transfer it to the genus Pseudodrobna[43]
- A study on the anatomy and morphological variation in Beurlenia araripensis, based on data from fossil samples from the Crato Formation (Brazil), is published by Barros et al. (2021).[44]
- A study on evolutionary trends in sexual dimorphism of cytheroid ostracods from the Gulf and Atlantic coastal plain from the Late Cretaceous to the late Eocene is published by Matzke-Karasz & Smith (2021).[45]
Insects
Trilobites
New taxa
Name | Novelty | Status | Authors | Age | Type locality | Location | Notes | Images |
---|---|---|---|---|---|---|---|---|
Sp. nov |
In press |
Wernette et al. |
Cambrian (Furongian) |
Myet-Ye Formation |
||||
Sp. nov |
Valid |
Van Viersen |
||||||
Dohmiella pooka[47] |
Sp. nov |
Valid |
Van Viersen |
Devonian (Eifelian) |
||||
Sp. nov |
Valid |
Peel |
A member of the family Alokistocaridae. |
|||||
Sp. nov |
Valid |
Peel |
Cambrian (Guzhangian) |
Blue Cliffs Formation |
A member of the family Bolaspididae. |
|||
Sp. nov |
Valid |
Peel |
Telt Bugt Formation |
A member of the family Zacanthoididae. |
||||
Sp. nov |
Valid |
Van Viersen |
Devonian (Eifelian) |
|||||
Sp. nov |
Valid |
Adrain & Karim |
Possibly a member of the family Dimeropygidae. |
|||||
Gonioteloides pankowskii[50] |
Sp. nov |
Valid |
Adrain & Karim |
Ordovician (Tremadocian) |
Possibly a member of the family Dimeropygidae. |
|||
Sp. nov |
Valid |
Van Viersen & Lerouge |
Devonian (Emsian) |
A member of the family Proetidae. |
Research
- A study on middle–late Cambrian trilobite diversity patterns in South China is published by Zhang et al. (2021).[52]
- Sun, Zeng & Zhao (2021) describe digestive structures of representatives of five trilobite genera from the Cambrian Mantou Formation and Zhangxia Formation (Liaoning, China).[53]
- Hou, Hughes & Hopkins (2021) report structural details of the upper limb branch of Triarthrus eatoni and Olenoides serratus, and interpret their findings as indicating that the upper limb branch of trilobites served a respiratory function.[54]
- A study on the morphology of Redlichia rex and Olenoides serratus, aiming to determine whether these trilobites were adapted for durophagy, is published by Bicknell et al. (2021).[55]
- A study exploring the existence and the nature of growth gradients along the main body axis of Oryctocarella duyunensis is published by Dai et al (2021), who interpret O. duyunensis as the first trilobite with documented determinate growth.[56]
- Description of all meraspid stages of Oryctocarella duyunensis, based on data from specimens from the Cambrian Balang Formation (Hunan, South China), is published by Dai et al. (2021).[57]
- A study on the long-term evolutionary history of Devonian trilobites in North Africa is published by Bault et al. (2021).[58]
- Evidence from trace and body fossils indicative of the presence of trilobites in brackish-water settings is presented by Mángano et al. (2021).[59]
- A study on the chemical changes in the exoskeleton of trilobites induced by diagenesis, based on data from pygidia of Athabaskia anax from the Miaolingian of San Isidro (Argentina), is published by D'Angelo et al. (2021), is published by D'Angelo et al. (2021), who argue that some morphological characteristics of the trilobite pygidia are in fact results of chemical and structural changes taking place during fossilization, and evaluate possible systematic implications of the chemical data, advising caution when using morphological characteristics of the exoskeletons to establish new taxa.[60]
- The study on the internal structures of eyes of trilobites belonging to the genera Asaphus and Archegonus published by Scholtz, Staude & Dunlop (2019)[61] is criticized by Schoenemann & Clarkson (2021).[62][63]
- A study on the biomechanics of the trilobite cephalon is published by Esteve et al. (2021), who interpret their findings as indicating that in the sutured trilobites the cephalon was able to withstand greater stresses than in their non‐sutured counterparts, and argue that the ability to withstand greater burrowing loads enabled trilobites to successfully invade bioturbated and more consolidated sediments during the Cambrian substrate revolution.[64]
Other arthropods
New taxa
Name | Novelty | Status | Authors | Age | Type locality | Location | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Valid |
Van Roy et al. |
A member of Thylacocephala. Genus includes new species B. libori. |
|||||
Gen. et sp. nov |
Valid |
Laville, Haug & Haug |
Carboniferous (middle Pennsylvanian) |
A member of Thylacocephala. The type species is E. keithflinti. |
||||
Gen. et sp. nov |
In press |
Bicknell, Hecker & Heyng |
A member of Xiphosura belonging to the family Austrolimulidae. Genus includes new species F. pochankei. |
|||||
Sp. nov |
Valid |
Riquelme & Hernández-Patricio in Riquelme, Hernández-Patricio & Álvarez-Rodríguez |
A millipede belonging to the family Pyrgodesmidae. |
|||||
Gen. et sp. nov |
Valid |
Lamsdell et al. |
A horseshoe crab. Genus includes new species O. latus. |
|||||
Sp. nov |
Valid |
Jin et al. |
Cambrian |
|||||
Gen. et sp. nov |
Valid |
Van Roy et al. |
Ordovician (Sandbian) |
Letná Formation |
A member of Thylacocephala. Genus includes new species P. irenae. |
Research
- New information on the anatomy of the head of Fuxianhuia is presented by Aria, Zhao & Zhu (2021), who interpret fuxianhuiids as mandibulates.[71]
- Revision of the morphological diversity, relationships and taxonomy of Early Triassic thylacocephalans is published by Laville et al. (2021).[72]
- Description of new fossil material of Mayrocaris bucculata from the Solnhofen Limestone, providing new information on the anatomy of this thylacocephalan, is published by Laville et al. (2021), who evaluate the implications of these fossils for the knowledge of the body organization and phylogenetic affinities of thylacocephalans.[73]
- A fossil larva lacking segmentation of the carapace, closely resembling the trilobite protaspis, is described from the Ordovician (Darriwilian) of central Siberia by Dzik (2021), found associated with other skeletal elements of the angarocaridid Girardevia;[74] however, Lerosey-Aubril & Laibl (2021) subsequently interpret this specimen as actually belonging to the trilobite genus Isotelus or a related taxon, and conclude that protaspid larvae represent a developmental trait unique to trilobites.[75][76]
- Redescription and a study on the phylogenetic relationships of Prolimulus woodwardi is published by Lustri, Laibl & Bicknell (2021).[77]
- A study on the anatomy and phylogenetic relationships of Parioscorpio venator is published by Anderson et al. (2021).[78]
General research
- A study on the evolution of the arthropod labrum is published by Budd (2021), who reevaluates the morphology of the Cambrian stem-euarthropod Parapeytoia and evaluates its implications for the knowledge of the origin of the labrum.[79]
Brachiopods
Name | Novelty | Status | Authors | Age | Type locality | Location | Notes | Images |
---|---|---|---|---|---|---|---|---|
Sp. nov |
Valid |
Popov & Nikitina in Popov et al. |
A kutorginide brachiopod. |
|||||
Sp. nov |
Valid |
Blodgett et al. |
A member of Pentamerida belonging to the family Gypidulidae. |
|||||
Sp. nov |
Valid |
Serobyan et al. |
Devonian (Famennian) |
An athyride brachiopod. |
||||
Sp. nov |
Valid |
Lavié, Mestre & Carrera |
Ordovician |
An acrotretid brachiopod. |
||||
Gen. et sp. nov |
Valid |
Popov et al. |
A rhynchonellide brachiopod. Genus includes new species K. granulata. |
|||||
Gen. et sp. nov |
Valid |
Popov et al. |
Silurian (Aeronian) |
Shabdjereh Formation |
A spiriferide brachiopod. Genus includes new species L. alatus. |
|||
Gen. et sp. nov |
Valid |
Lavié, Mestre & Carrera |
Ordovician |
San Juan Formation |
An obolid brachiopod. Genus includes new species L. diminuta. |
|||
Sp. nov |
Valid |
Popov et al. |
Silurian (Aeronian) |
Shabdjereh Formation |
A spiriferide brachiopod. |
|||
Sp. nov |
Valid |
Popov & Nikitina in Popov et al. |
Cambrian (Wuliuan) |
Athei Formation |
A protorthide brachiopod. |
|||
Sp. nov |
Valid |
Rezende & Isaacson |
Devonian |
Ponta Grossa Formation |
A member of Orthotetida. |
|||
Nom. nov |
Valid |
García-Alcalde |
Early Devonian |
A terebratulid brachiopod; a replacement name for Xana García-Alcalde (1972). |
||||
Sp. nov |
In press |
Guo, Chen & Liao |
Early Carboniferous |
Molluscs
Echinoderms
New taxa
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Sp. nov |
Valid |
Néraudeau & Mouty |
Late Cretaceous (Cenomanian) |
A sea urchin belonging to the family Archiaciidae. |
||||
Gen. et 2 sp. nov |
In press |
Thuy & Numberger-Thuy |
A brittle star belonging to the group Ophiurida. The type species is B. colbachi; genus also includes B. muenzbergerae. |
|||||
Gen. et sp. nov |
Hunter & Ortega-Hernández |
Early Ordovician |
A somasteroid asterozoan. The type species is C. fezouataensis. |
|||||
Sp. nov |
Valid |
Roux, Martinez & Vizcaïno |
Eocene (Ypresian) |
A crinoid belonging to the family Rhizocrinidae. |
||||
Sp. nov |
In press |
Gale |
Late Cretaceous (Campanian) |
A crinoid. |
||||
Sp. nov |
In press |
Thuy & Numberger-Thuy |
Early Jurassic (Toarcian) |
A brittle star belonging to the family Ophionereididae. |
||||
Gen. et sp. nov |
In press |
Gale |
Late Cretaceous (Campanian) |
A crinoid. Genus includes new species D. alumensis. |
||||
Sp. nov |
In press |
El Qot |
Early Cretaceous (Albian) |
A sea urchin. |
||||
Gen. et sp. nov |
Valid |
Roux, Martinez & Vizcaïno |
Eocene (Ypresian) |
A crinoid belonging to the family Rhizocrinidae. Genus includes new species G. amphoraformis. |
||||
Sp. nov |
In press |
Gale |
Late Cretaceous (Campanian) |
A crinoid. |
||||
Sp. nov |
Valid |
Roux, Martinez & Vizcaïno |
Eocene (Ypresian) |
A crinoid belonging to the family Holopodidae. |
||||
Sp. nov |
In press |
Thuy & Numberger-Thuy |
Early Jurassic (Toarcian) |
A brittle star belonging to the group Euryophiurida. |
||||
Sp. nov |
In press |
Thuy & Numberger-Thuy |
Early Jurassic (Toarcian) |
A brittle star belonging to the group Ophioscolecida and the family Ophioscolecidae. |
||||
Sp. nov |
In press |
Thuy & Numberger-Thuy |
Early Jurassic (Toarcian) |
A brittle star belonging to the group Ophiurida and the family Astrophiuridae. |
||||
Sp. nov |
In press |
Thuy & Numberger-Thuy |
Early Jurassic (Toarcian) |
A brittle star belonging to the group Ophiurida and the family Ophiomusaidae. |
||||
Gen. et sp. et comb. nov |
In press |
Thuy & Numberger-Thuy |
Early Jurassic (Sinemurian-Toarcian) |
A brittle star belonging to the group Ophiurida and the family Ophiopyrgidae. The type species is O. tennanti; genus also includes "Ophiura" astonensis Hess (1964). |
||||
Sp. nov |
In press |
Thuy & Numberger-Thuy |
Early Jurassic (Toarcian) |
A brittle star belonging to the group Ophiurida and the family Ophiopyrgidae. |
||||
Sp. nov |
Valid |
Roux, Martinez & Vizcaïno |
Eocene (Ypresian) |
A crinoid belonging to the family Rhizocrinidae. |
||||
Sp. nov |
In press |
Gale |
Late Cretaceous (Campanian) |
A crinoid. |
||||
Sp. nov |
Valid |
Donovan & Fearnhead |
Early Devonian |
A crinoid. |
||||
Gen. et sp. nov |
In press |
El Qot |
Late Cretaceous (Cenomanian) |
A sea urchin. Genus includes new species S. rhombohedralis. |
||||
Sp. nov |
In press |
Thuy & Numberger-Thuy |
Early Jurassic (Toarcian) |
A brittle star belonging to the group Ophioscolecida and the family Ophioleucidae. |
||||
Gen. et sp. et comb. nov |
In press |
Thuy & Numberger-Thuy |
Early Jurassic (Sinemurian to Toarcian) |
A brittle star belonging to the group Ophiurida. The type species is T. desdemonia; genus also includes "Ophiomusium" sinemurensis Kutscher & Hary (1991). |
||||
Gen. et sp. nov |
Valid |
Semenov et al. |
A hybocrinid crinoid. Genus includes new species T. schmidti. |
Research
- A study on the functional efficiency of hydrospires of blastoids, evaluating their potential significance for longer survival of blastoids than other blastozoan echinoderms, is published by Paul (2021).[96]
- A study on extinction selectivity and changes in taxonomic, morphological and ecological diversity of diplobathrid crinoids throughout their evolutionary history is published by Cole & Hopkins (2021).[97]
Conodonts
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Sp. nov |
In press |
Karádi et al. |
A member of the family Gondolellidae. |
|||||
Ancyrogondolella goldingi[98] |
Sp. nov |
In press |
Karádi et al. |
Late Triassic (Norian) |
A member of the family Gondolellidae. |
|||
Sp. nov |
Valid |
Yan & Wu |
||||||
Sp. nov |
Valid |
Barrick, Sundgren & McAdams |
||||||
Caudicriodus murphyi[100] |
Sp. nov |
Valid |
Barrick, Sundgren & McAdams |
Devonian (Lochkovian) |
||||
Sp. nov |
In press |
Świś |
Devonian (Famennian) |
|||||
Sp. nov |
In press |
Karádi et al. |
Late Triassic (Norian) |
A member of the family Gondolellidae. |
||||
Epigondolella kozjanskoensis[98] |
Sp. nov |
In press |
Karádi et al. |
Late Triassic (Norian) |
A member of the family Gondolellidae. |
|||
Epigondolella ritae[98] |
Sp. nov |
In press |
Karádi et al. |
Late Triassic (Norian) |
A member of the family Gondolellidae. |
|||
Epigondolella senovoensis[98] |
Sp. nov |
In press |
Karádi et al. |
Late Triassic (Norian) |
A member of the family Gondolellidae. |
|||
Epigondolella slovenica[98] |
Sp. nov |
In press |
Karádi et al. |
Late Triassic (Norian) |
A member of the family Gondolellidae. |
|||
Sp. nov |
In press |
Li & Lai in Li et al. |
Late Triassic (Carnian) |
Dengdengqiao Formation |
||||
Sp. nov |
In press |
Gómez et al. |
Silurian (Ludfordian) to Devonian (Lochkovian) |
|||||
Sp. nov |
In press |
Rigo & Du in Du et al. |
Late Triassic (Norian and Rhaetian) |
|||||
Sp. nov |
Valid |
Barrick, Sundgren & McAdams |
||||||
Sp. nov |
Valid |
Yang et al. |
Fish
New taxa
Jawless vertebrates
Name | Novelty | Status | Authors | Age | Type locality | Location | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Valid |
Liu et al. |
A member of Galeaspida belonging to the group Eugaleaspidiformes. The type species is J. retrospina. |
|||||
Gen. et sp. nov |
In press |
Jiang et al. |
Early Devonian |
A member of Galeaspida. Genus includes new species Q. elaia. |
Placoderms
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Jobbins et al. |
Devonian (Givetian) |
A member of Arthrodira belonging to the family Plourdosteidae. The type species is L. ziregensis. |
Acanthodians
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Sp. nov |
Valid |
Li et al. |
||||||
Nostolepis qujingensis[109] |
Sp. nov |
Valid |
Li et al. |
Devonian (Lochkovian) |
Xitun Formation |
Cartilaginous fishes
Name | Novelty | Status | Authors | Age | Type locality | Location | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Vullo et al. |
Late Cretaceous (Turonian) |
A probable planktivorous shark of uncertain phylogenetic placement, possibly a member of Lamniformes. The type species is A. milarcae. |
|||||
Gen. et sp. nov |
Valid |
Hodnett et al. |
A medium-sized ctenacanthiform shark known from a complete skeleton with soft tissue. The type species is D. hoffmanorum. |
|||||
Gen. et sp. nov |
Valid |
Stumpf et al. |
Late Jurassic (Tithonian) |
A member of the family Hybodontidae. The type species is D. maiseyi. |
||||
Gen. et sp. nov |
Valid |
Collareta et al. |
A member of Rajiformes, possibly a skate. The type species is N. wardi. |
|||||
Sp. nov |
Valid |
Ivanov |
||||||
Sp. nov |
In press |
Jambura, Stumpf & Kriwet |
Late Cretaceous (Cenomanian) |
Ray-finned fishes
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Figueroa, Weinschütz & Friedman |
Middle Devonian or older |
Paraná Basin |
An early ray-finned fish. Genus includes new species A. ferox. |
||||
Sp. nov |
Valid |
Nam, Nazarkin & Bannikov |
Middle Miocene |
A species of Auxis. |
||||
Gen. et sp. nov |
In press |
Hacker & Shimada |
A member of Ichthyodectiformes. Genus includes new species B. carteri. |
|||||
Gen. et comb. nov |
Valid |
Schwarzhans, Milàn & Carnevale |
Kerteminde Marl |
A member of the family Macrouridae. The type species is "Hymenocephalus" rosenkrantzi Schwarzhans (2003). |
||||
Gen. et comb. nov |
Valid |
Taverne & Capasso |
A member of the family Pycnodontidae. The type species is "Proscinetes" pillae Capasso (2007). |
|||||
Sp. nov |
In press |
Newman et al. |
Devonian (Givetian) |
|||||
Gen. et sp. nov |
Valid |
Cantalice, Than‐Marchese & Villalobos‐Segura |
A member of Acanthopterygii of uncertain phylogenetic placement. Genus includes new species C. alvaradoi. |
|||||
Sp. nov |
Valid |
Ma, Xu & Geng |
A member of the family Colobodontidae. |
|||||
Sp. nov |
In press |
Ebersole, Cicimurri & Stringer |
A member of the family Gobiidae. |
|||||
Gen. et sp. nov |
Valid |
Chen et al. |
A member of Clupeomorpha belonging to the group Ellimmichthyiformes. The type species is G. superstes. |
|||||
Sp. nov |
In press |
Ren & Xu |
Middle Triassic (Anisian) |
|||||
Gen. et sp. nov |
Valid |
Yabumoto & Nazarkin |
Late Miocene |
Koshikawa Formation |
A member of the family Scorpaenidae. Genus includes new species R. sakurai. |
|||
Sp. nov |
Valid |
Renesto, Magnani & Stockar |
||||||
Gen. et sp. nov |
In press |
Stringer & Schwarzhans |
Late Cretaceous (Maastrichtian) |
Possibly a member of Polymixiiformes. Genus includes new species S. bourdoni. |
Research
- A study aiming to determine whether the earliest vertebrates may have swum under various conditions without a clearly-differentiated tail fin, based on data from an abstracted model of Metaspriggina walcotti, is published by Rival, Yang & Caron (2021).[130]
- Miyashita et al. (2021) report larval and juvenile forms of four stem lampreys from the Paleozoic era (Hardistiella, Mayomyzon, Pipiscius and Priscomyzon), including a hatchling-to-adult growth series of Priscomyzon, and report that the studied larvae display features that are otherwise unique to adult modern lampreys, and lack the defining traits of ammocoetes.[131]
- A study on the morphological and functional diversity of osteostracan and galeaspid headshields, and on its implications for the knowledge of the ecology of the immediate jawless relatives of jawed vertebrates, is published by Ferrón et al. (2021).[132]
- A study on the histology of the dermal skeleton in Procephalaspis oeselensis, Aestiaspis viitaensis, Dartmuthia gemmifera and four species of Tremataspis is published by Bremer et al. (2021), who interpret their findings as indicative of the emergence of the complex pore‐canal system in Tremataspis through the modification of the structures already present in other taxa.[133]
- A study on the morphology of the earliest osteocytes in Tremataspis mammillata and Bothriolepis trautscholdi is published by Haridy et al. (2021), who interpret their findings as indicating that the earliest known osteocytes in the fossil record had similar morphology and likely similar physiological capabilities to their modern counterparts, and attempt to determine initial driver favoring evolution of cellular (osteocytic) over acellular (anosteocytic) bones in vertebrates.[134]
- Zhu et al. (2021) use CT scanning to reveal the endocast of Brindabellaspis stensioi, and evaluate the implications of its anatomy for the knowledge of the phylogenetic relationships of early jawed vertebrates.[135]
- Redescription of the anatomy of the headshield of Parayunnanolepis xitunensis is published by Wang & Zhu (2021).[136]
- Description of new fossil material of Palaeacanthaspis vasta from the Devonian (Lochkovian) Chortkiv Formation (Ukraine), and a study on the phylogenetic relationships of this species, is published by Dupret et al. (2021).[137]
- A study on the development of teeth in acanthodians, and on its implications for the knowledge of the evolution of teeth of jawed vertebrates, is published by Rücklin et al. (2021).[138]
- Description of the first known skull remains of Onchopristis numidus from the Cretaceous Kem Kem Group (Morocco), and a study on the anatomy and phylogenetic relationships of this species, is published by Villalobos-Segura et al. (2021), who name a new family Onchopristidae.[139]
- New, exceptionally well‐preserved skeleton of Asteracanthus ornatissimus, preserved with teeth that markedly differ from other teeth referred to Asteracanthus, is described from the Tithonian Altmühltal Formation (Germany) by Stumpf et al. (2021), who interpret this specimen as indicating that Asteracanthus and Strophodus represent two valid genera distinct from all other hybodontiforms.[140]
- A study on the biomechanics of teeth of five species of Otodus, aiming to assess the functional significance of morphological trends in otodontid teeth and to test whether the morphology of otodontid teeth enabled the transition from piscivory to predation on marine mammals and the evolution of titanic body sizes, is published by Ballell & Ferrón (2021)[141]
- A study on growth patterns, reproductive biology and likely lifespan of Otodus megalodon is published by Shimada et al. (2021).[142]
- Perez, Leder & Badaut (2021) present a novel method for estimating body size in fossil lamniform sharks, and attempt to determine the body size of Otodus megalodon.[143]
- Revision of the fossil record of the extant tiger shark and the extinct members of the tiger shark lineage is published by Türtscher et al. (2021).[144]
- Redescription of Striatolamia tchelkarnurensis is published by Malyshkina (2021).[145]
- Shark teeth which might represent the first occurrence of the blacknose shark in the Pacific Ocean are described from the Pliocene Upper Onzole Formation (Ecuador) by Collareta et al. (2021), who evaluate the implications of this finding for the knowledge of the evolutionary history of the blacknose shark and the whitenose shark.[146]
- A platysomid specimen, representing the earliest deep-bodied actinopterygian reported to date, is described from the Carboniferous (Tournaisian) Horton Bluff Formation (Canada) by Wilson, Mansky & Anderson (2021), who evaluate the implications of this findings for the knowledge of the evolution of early ray-finned fishes.[147]
- A review of the fossil record of Early–Middle Triassic marine bony fishes, aiming to determine the implications of poor fossil record from the late Olenekian-early middle Anisian interval on the knowledge of the Triassic radiation of bony fishes, is published by Romano (2021).[148]
- A diverse assemblage of late Maastrichtian and Paleocene ray-finned fishes is described from Evrytania (Greece) by Argyriou & Davesne (2021).[149]
- A study on the morphological diversity and evolution of pycnodontiforms is published by Cawley et al. (2021).[150]
- A study on fossil crushing dentitions of Pycnodus zeaformis and P. maliensis, providing evidence of a distinct pattern of gap‐filling tooth addition in pycnodonts, with individual large teeth replaced by multiple small teeth, is published by Collins & Underwood (2021).[151]
- A study on the evolutionary history of lanternfishes, primarily based on the fossil record of otoliths, is published by Schwarzhans & Carnevale (2021).[152]
- A study on the phylogenetic relationships of extant and fossil coelacanths is published by Toriño, Soto & Perea (2021).[153]
- A study on the morphology and histology of the scales of Miguashaia bureaui, and on its implications for the knowledge of the evolution of the squamation in coelacanths, is published by Mondéjar‐Fernández et al. (2021).[154]
- An ossified lung of a mawsoniid coelacanth is described from the Maastrichtian of Oued Zem (Morocco) by Brito et al. (2021), representing the last known record of a Mesozoic coelacanth and the first known occurrence of coelacanths in the phosphate deposits of North Africa.[155]
- A study on the evolution of feeding modes among tetrapodomorphs, as indicated by the anatomy of the skull of Tiktaalik roseae, is published by Lemberg, Daeschler & Shubin (2021), who report the simultaneous occurrence of anatomical modifications of the skull for prey capture through biting, as well as joint morphologies suggestive of cranial kinesis that is also present in suction-feeding fish.[156]
Amphibians
New taxa
Name | Novelty | Status | Authors | Age | Type locality | Location | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Valid |
Werneburg, Schneider & Lucas |
A dvinosauroid temnospondyl. The type species is B. kinneyi. |
|||||
Sp. nov |
Valid |
Liu & Chen |
Late Permian |
|||||
Sp. nov |
Valid |
Roček, Rage & Venczel |
||||||
Palaeobatrachus minutus[159] |
Sp. nov |
Valid |
Roček, Rage & Venczel |
|||||
Gen. et sp. nov |
Valid |
Rage et al. |
Eocene |
A frog belonging to the group Ranoidea. The type species is R. ornata. |
Research
- A study on the function and evolution of forelimbs of early tetrapods, based on data from three-dimensional models of bones and muscles of forelimbs of Eusthenopteron foordi, Acanthostega gunnari and Pederpes finneyae, is published by Molnar et al. (2021).[161]
- A study on the locomotor capabilities of tetrapods from the earliest Carboniferous Blue Beach site (Nova Scotia, Canada) is published by Lennie et al. (2021).[162]
- A study on the early evolution of long bone elongation and bone marrow in tetrapods, based on data from temnospondyls (Apateon and Metoposaurus) and seymouriamorphs (Seymouria and Discosauriscus), is published by Estefa et al. (2021), who find the terrestrial Permian seymouriamorphs to be the oldest known tetrapods exhibiting a centralized marrow organization of long bones (which allows production of blood cells as in extant amniotes), and argue that the migration of blood-cell production in long bones probably wasn't an exaptation predating the water-to-land transition.[163]
- A study on the skeletal anatomy of the holotype specimen of Ichthyerpeton bradleyae is published by Ó Gogáin & Wyse Jackson (2021).[164]
- Description of the anatomy of the postcranial skeleton of Whatcheeria deltae is published by Otoo et al. (2021).[165]
- A study on the anatomy and phylogenetic relationships of "Cheliderpeton" lellbachae is published by Schoch (2021), who transfers this species to the genus Glanochthon in the family Sclerocephalidae.[166]
- A study on the histology of different-sized femora and vertebra of specimens of Platyoposaurus stuckenbergi is published by Uliakhin, Skutschas & Saburov (2021).[167]
- A study on the anatomy and phylogenetic relationships of Tertrema acuta is published by Slodownik, Mörs & Kear (2021).[168]
- Redescription of the metoposaurid fossil material from the Upper Triassic Zions View locality (New Oxford Formation; Pennsylvania, United States) is published by Gee & Jasinski (2021), who assign this material to the species Anaschisma browni, expanding known geographic range of this taxon.[169]
- A study on the anatomy and phylogenetic relationships of Timonya anneae and Procuhy nazariensis is published by Marsicano et al. (2021).[170]
- A study on the anatomy and phylogenetic relationships of Macrerpeton huxleyi is published by Schoch & Milner (2021).[171]
- Description of a new specimen of Conjunctio from the Permian Cutler Formation (Colorado, United States), and a study on the phylogenetic relationships of this genus, is published by Gee et al. (2021).[172]
- New fossil material of Micropholis stowi, expanding known geographic range of this species, is described from the lower Fremouw Formation (Halfmoon Bluff, Antarctica) by Gee & Sidor (2021).[173]
- New early adult specimen of Milnererpeton huberi, providing new information on the ontogenetic development of amphibamiform temnospondyls, is described from the Carboniferous (Kasimovian) Atrasado Formation (New Mexico, United States) by Werneburg, Schneider & Lucas (2021).[174]
- An early Campanian assemblage of anuran bones, suggestive of high local species richness of frogs, is described from the Aguja Formation (Texas, United States) by Wick (2021).[175]
- Description of new fossil material of Hungarobatrachus szukacsi from the Upper Cretaceous (Santonian) Csehbánya Formation (Hungary), and a study on the anatomy and phylogenetic relationships of this species, is published by Venczel, Szentesi & Gardner (2021).[176]
- Revision of the fossil record of the family Ceratophryidae is published by Gómez & Turazzini (2021).[177]
- Revision of the fossil material of Mesozoic temnospondyls and anurans housed in the collections of the Sirindhorn Museum and the Palaeontological Research and Education Centre of Mahasarakham University (Thailand), including fossils of brachyopids resembling the Chinese forms, is published by Nonsrirach, Manitkoon & Lauprasert (2021).[178]
Reptiles
Synapsids
Non-mammalian synapsids
New taxa
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et comb. nov |
Valid |
Kammerer & Ordoñez |
A kannemeyeriid dicynodont, the type species is "Kannemeyeria" argentinensis. |
|||||
Sp. nov |
Valid |
Panciroli et al. |
A docodont. |
|||||
Gen. et comb. nov |
Valid |
Panciroli et al. |
Middle Jurassic (Bathonian) |
A docodont; a new genus for "Borealestes" mussettae Sigogneau−Russell (2003). |
||||
Gen. et sp. nov |
Valid |
Mao et al. |
A cynodont belonging to the family Tritylodontidae. Genus includes new species F. sinensis. |
|||||
Gen. et sp. nov |
In press |
Sidor, Tabor & Smith |
Late Permian |
A burnetiamorph biarmosuchian. Genus includes new species I. luangwensis. |
||||
Sp. nov |
Valid |
Kammerer & Ordoñez |
A species of Kannemeyeria. |
|||||
Gen. et sp. nov |
Valid |
Kammerer & Sidor |
||||||
Sp. nov |
Valid |
Liu |
Late Permian |
A dicynodontoid dicynodont. |
Research
- A study on the evolution of the vertebral column in synapsids is published by Jones et al. (2021), who interpret their findings as refuting the idea that the transition from non-mammalian synapsids to mammals involved a shift from reptile-like lateral bending of the backbone to sagittal bending, and argue that non-mammalian synapsids were characterized by their own unique functional regime of the vertebral column, distinct from that of extant reptiles and amphibians.[185]
- A study comparing the forelimb morphology in extant mammals and fossil non-mammalian synapsids, aiming to determine whether extant mammals are good ecomorphological analogues for extinct synapsids, whether examples of ecomorphological convergence can be found among synapsids, and whether evolutionary history determined available functional solutions in synapsid forelimbs, is published by Lungmus & Angielczyk (2021).[186]
- A study comparing the morphology of the maxillary canal of Heleosaurus scholtzi, Varanosaurus acutrostris, Orovenator mayorum and Prolacerta broomi, and evaluating the implications of the morphology of the maxillary canal for the knowledge of the phylogenetic placement of varanopids, is published by Benoit et al. (2021).[187]
- A study on the paleoneurology and likely paleobiology of Anteosaurus magnificus is published by Benoit et al. (2021).[188]
- New specimen of Lanthanostegus mohoii, providing new information on the anatomy of the skull of this dicynodont and providing the first direct correlation between the lower Abrahamskraal Formation at Jansenville on the eastern side of the Karoo Basin and the southwestern part of this basin, is described by Rubidge, Day & Benoit (2021).[189]
- New burrow casts containing skeletons of Diictodon, including associated remains of adult and infant specimens, are described by Smith et al. (2021), who consider it likely that portions of underground burrows produced Diictodon by were facultatively used as brood chambers.[190]
- Redescription and a study on the phylogenetic relationships of Kunpania scopulusa is published by Angielczyk, Liu & Yang (2021).[191]
- A study on the bone histology and likely life history of specimens of Lystrosaurus from the Lower Triassic Turpan Basin (Xinjiang, China), comparing them with specimens from South Africa, is published by Han, Zhao & Liu (2021).[192]
- A new postcranial specimen of a stahleckeriid dicynodont, possibly of Stahleckeria, is described from the Chañares Formation, representing the oldest record of stahleckeriine dicynodonts from the Ischigualasto-Villa Unión Basin in Argentina.[193]
- A study on the quality of the early cynodont fossil record in time and space, and on its implications for the understanding of the group's evolutionary history, is published by Varnham, Mannion & Kammerer (2021).[194]
- A study on the anatomy and variation of the stapes in Thrinaxodon and Galesaurus is published by Gaetano & Abdala (2021).[195]
- A study on the morphology of the nasal cavity of Exaeretodon riograndensis and Siriusgnathus niemeyerorum is published by Franco et al. (2021).[196]
- A study on the morphology of the endocast of a specimen of Riograndia guaibensis from the Linha São Luiz site (Candelária Sequence of the Santa Maria Supersequence, Brazil) is published by Kerber et al. (2021).[197]
- New specimen of the Middle Jurassic haramiyidan Vilevolodon diplomylos with well-preserved malleus, incus and ectotympanic is described by Wang et al. (2021).[198]
Mammals
Other animals
New taxa
Name | Novelty | Status | Authors | Age | Type locality | Country | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Valid |
Moczydłowska in Moczydłowska et al. |
A member of Eumetazoa of uncertain phylogenetic placement. The type species is A. formosus. |
|||||
Sp. nov |
Valid |
Maletz & Ahlberg |
A graptolite. |
|||||
Arienigraptus delicatus[200] |
Sp. nov |
Valid |
Maletz & Ahlberg |
Ordovician (Darriwilian) |
A graptolite. |
|||
Arienigraptus robustus[200] |
Sp. nov |
Valid |
Maletz & Ahlberg |
Ordovician (Dapingian) |
A graptolite. |
|||
Sp. nov |
In press |
Sánchez-Beristain & García-Barrera in Sánchez-Beristain, García-Barrera & Juárez-Aguilar |
Late Cretaceous |
A chaetetid demosponge. |
||||
Gen. et sp. nov |
Valid |
Pates et al. |
A member of Radiodonta belonging to the family Hurdiidae. The type species is B. cooperi. |
|||||
Gen. et sp. nov |
Valid |
Moczydłowska in Moczydłowska et al. |
Ediacaran |
Stáhpogieddi Formation |
A member of Eumetazoa of uncertain phylogenetic placement. The type species is C. elegantis. |
|||
Sp. nov |
Valid |
Vinn & Eyzenga |
Late Ordovician |
A cornulitid tubeworm. |
||||
Sp. nov |
Valid |
Claybourn et al. |
||||||
Gen. et sp. nov |
Valid |
Moczydłowska in Moczydłowska et al. |
Ediacaran |
Stáhpogieddi Formation |
A member of Eumetazoa of uncertain phylogenetic placement. The type species is F. crenulata. |
|||
Gen. et comb. nov |
Valid |
Wu et al. |
A member of Radiodonta belonging to the family Tamisiocarididae. The type species is "Anomalocaris" saron Hou, Bergström & Ahlberg (1995); genus also includes "Anomalocaris" magnabasis Pates et al. (2019). |
|||||
Gen. et sp. et comb. nov |
In press |
Wu et al. |
Cambrian |
A member of Radiodonta. Genus includes new species L. lupata, as well as "Anomalocaris" pennsylvanica Resser (1929). |
||||
Gen. et sp. nov |
In press |
Samant et al. |
Late Cretaceous (Maastrichtian) |
A sponge belonging to the family Palaeospongillidae. Genus includes new species P. cretacea. |
||||
Sp. nov |
Valid |
Luo et al. |
Cambrian |
A sponge. |
||||
Sp. nov |
Valid |
Kozłowska & Bates |
A graptolite belonging to the family Retiolitidae. |
|||||
Sp. nov |
Valid |
Jiao et al. |
Wulongqing Formation |
A member of Radiodonta belonging to the family Anomalocarididae. |
||||
Sp. nov |
Valid |
Ling et al. |
A sponge of uncertain phylogenetic placement, possibly with protomonaxonid affinities. |
|||||
Sp. nov |
Valid |
Luo et al. |
Cambrian |
Shuijingtuo Formation |
A sponge. |
|||
Gen. et sp. nov |
In press |
Dieni & Massari |
Early Cretaceous (Berriasian) |
A microserpulid. Genus includes new species T. coralliophila. |
||||
Sp. nov |
In press |
Wei et al. |
A vauxiid sponge. |
|||||
Vauxia pregracilenta[213] |
Sp. nov |
In press |
Wei et al. |
Cambrian Stage 3 |
A vauxiid sponge. |
Research
- A study aiming to identify characters of Kimberella, Ikaria, Dickinsonia and Tribrachidium controlled by conserved developmental processes, as well as genetic elements likely responsible for their expression, is published by Evans, Droser & Erwin (2021), who also attempt to determine phylogenetic positions of these taxa relative to extant animals.[214]
- Structures interpreted as traces of motor activity of Dickinsonia are reported by Ivantsov & Zakrevskaya (2021), who interpret the studied traces as indicating that Dickinsonia was capable of both attachment and mobility.[215]
- A study aiming to determine the feeding mode of Arkarua adami is published by Cracknell et al. (2021).[216]
- Shore et al. (2021) report the first three-dimensional, pyritized preservation of soft tissue in Namacalathus hermanastes from the Nama Group (Namibia), and evaluate the implications of this finding for the knowledge of the phylogenetic relationships of this animal.[217]
- A new assemblage of fossil eggs, embryos attributable to the early scalidophoran Markuelia, and early post-embryonic developmental stages of camenellans is described from the Cambrian Stage 3 Salanygol Formation (Mongolia) by Steiner et al. (2021).[218]
- Redescription of Stanleycaris hirpex, and a study on the phylogenetic relationships of this species and on the functional specialization of the frontal appendages of this and other stem euarthropods, is published by Moysiuk & Caron (2021).[219]
Other organisms
New taxa
Name | Novelty | Status | Authors | Age | Type locality | Location | Notes | Images |
---|---|---|---|---|---|---|---|---|
Gen. et sp. nov |
Strother & Wellman in Strother et al. |
ca. 1 billion years old |
An organism of uncertain phylogenetic placement, possibly an early member of Holozoa. Genus includes new species B. brasieri. Appears to have differentiated multicellularity. |
|||||
Gen. et sp. nov |
Valid |
Le Renard et al. |
A fungus belonging to the group Dothideomycetes. Genus includes new species B. ostiolatum. |
|||||
Sp. nov |
Valid |
Haelewaters & Perreau in Perreau, Haelewaters & Tafforeau |
A fungus, a species of Columnomyces. |
|||||
Gen. et sp. nov |
Valid |
Taylor et al. |
A organism growing on the seafloor in a manner similar to Fractofusus and Beothukis. Genus includes new species G. samsoni. |
|||||
Gen. et sp. nov |
Valid |
Miao, Moczydłowska & Zhu |
Early Mesoproterozoic |
An organic-walled microfossil. Genus includes new species Q. clavatus. |
||||
Gen. et sp. nov |
Valid |
Krings, Serbet & Harper |
Early Devonian |
A fungus belonging to the group Chytridiomycota. Genus includes new species R. matryoshkae. |
Research
- Delarue et al. (2021) describe 3.4 billion years old microfossils preserved with a tail-like structure from the Strelley Pool Formation (Australia), and interpret the tail-like appendage as likely providing early microorganisms with movement capabilities.[227]
- Tang et al. (2021) describe dark discoidal, semicircular, or ovate structures preserved on fossil of early Neoproterozoic eukaryotes Tawuia and Sinosabellidites from North China, and interpret these structures as fossils of eukaryotic epibionts that lived on the surface of and may have benefited from an association with their Tawuia and Sinosabellidites hosts.[228]
- Exceptionally preserved specimens of Tawuia, providing new information on the anatomy of this organism, are described from the Tonian Liulaobei and Shiwangzhuang formations (China) by Tang et al. (2021), who interpret Tawuia as a coenocytic eukaryote, possibly a macroalga.[229]
- Well-preserved communities of large unbranched filamentous microorganisms, bearing morphological and ecological similarities with large sulfide-oxidizing bacteria such as Beggiatoa, are described from the Ediacaran Itajaí Basin (Brazil) by Becker-Kerber et al. (2021).[230]
- Microfossils which may represent early terrestrial fungi are described from the Ediacaran Doushantuo Formation (China) by Gan et al. (2021).[231]
- A Rhynie chert fossil Mycokidstonia sphaerialoides, originally interpreted as an ascomycete, is reclassified as a member of Glomeromycota belonging to the family Ambisporaceae by Walker et al. (2021).[232]
- Carboniferous organism Oochytrium lepidodendri, originally classified as a fungus, is reinterpreted as an oomycete by Strullu-Derrien et al. (2021).[233]
- Probable fossils of multicellular eukaryotic macroalgae (possibly with a green algal affinity) are described from the Tonian Dolores Creek Formation in the Wernecke Mountains (Canada) by Maloney et al. (2021), who interpret these fossils as likely to be some of the few green algae and some of the largest macroscopic eukaryotes yet recognized in the early Neoproterozoic, indicating that eukaryotic algae colonized marine environments by the early Neoproterozoic.[234]
- Zacaï et al. (2021) attempt to determine the potential timing of establishment of the latitudinal diversity gradient for early Paleozoic acritarchs and its evolution through time .[235]
History of life in general
- A study on the taphonomy of eukaryotic organelles, assessing the basis of the view that organelles decay too rapidly to be fossilized and evaluating the plausibility of the claims of organelles preserved in Proterozoic fossils, is published by Carlisle et al. (2021).[236]
- Evidence of the presence of significant populations of both red and green algae ca. 1.4 billion years ago (600 million years earlier than previously recognized) is reported from the Xiamaling Formation (China) by Zhang et al. (2021).[237]
- A study on the major biotic transitions in the Phanerozoic fossil record of the benthic marine faunas is published by Rojas et al. (2021), who report evidence of three major biotic transitions (across the end-Cambrian, end-Permian, and mid-Cretaceous boundaries).[238]
- A study on changes of diversity of skeletonized marine invertebrates in the fossil record, evaluating the impact of dead clades walking on broader trends in Phanerozoic biodiversity, is published by Barnes, Sclafani & Zaffos (2021), who identify 70 invertebrate orders that experienced major diversity losses without recovery, but note that most of these taxa had a long duration after the drop in diversity, and many drops in diversity without recovery were not associated with mass extinction events.[239]
- Geyer & Landing (2021) report a hitherto unknown Cambrian Stage 3 Lagerstätte from the Amouslek Formation (Morocco), preserving the first relatively abundant fossils with exceptional preservation from the Cambrian of Morocco (and Africa).[240]
- A study on Carboniferous and early Permian tetrapod tracks, and on their implications for the knowledge of evolutionary changes in the anatomy of the trackmakers in and locomotion style close to the origin of amniotes, is published by Buchwitz et al. (2021).[241]
- A study on the impact of Permian mass extinctions on continental invertebrate infauna, based on data from the Iberian Basin (central Spain), is published by Buatois et al. (2021), who report evidence of a dramatic decrease in bioturbation intensity on land by the end of the Capitanian, coinciding with an increase in weathering intensity and acidic conditions, and a collapse in plant communities spanning the late Permian–Early Triassic in the Iberian Basin.[242]
- A review of the state of research on the Capitanian mass extinction event in the Karoo Basin (South Africa) is published by Day & Rubidge (2021).[243]
- Evidence from tetrapod fossil record from the Karoo Basin (South Africa) indicative of a protracted (∼1 Ma) extinction on land during the Permian-Triassic transition is presented by Viglietti et al. (2021).[244]
- Evidence of two pulses of extinction at the Permian–Triassic boundary caused by different environmental triggers is reported from the Liangfengya section in the South China Block by Li et al. (2021).[245]
- Revision of the Triassic record of tetrapod tracks is published by Klein & Lucas (2021).[246]
- A study on the diversity dynamics and evolution of the functional morphology of tetrapod herbivores throughout the Triassic and Early Jurassic is published by Singh et al. (2021).[247]
- Marchetti et al. (2021) revise the tetrapod (including dinosauromorph) footprint assemblage from the Quarziti del Monte Serra Formation (Ladinian of Italy), and interpret this assemblage and other findings of Ladinian dinosauromorph footprints as evidence of wide dispersal of dinosauromorphs as early as the Middle Triassic.[248]
- Zouhri et al. (2021) describe a diverse vertebrate fauna from the Eocene (Bartonian) Aridal Formation (Western Sahara), including 12 species of cartilaginous fishes, at least three species of turtles, at least two longirostrine crocodylian taxa, the oldest record of Pelagornis reported to date, and a proboscidean possibly belonging to the genus Barytherium.[249]
- A study on the age of escorias (glassy rock fragments similar to volcanic scoriae, likely products of extraterrestrial impacts) collected along the Pampean Atlantic coast from the "Irene" and Chapadmalal Formations (Argentina), and on their implications for the knowledge of the timing of late Miocene–Pliocene faunal succession in the Pampean Region, is published by Prevosti et al. (2021).[250]
- A study on the age of the most recent Pleistocene megafaunal specimens from Cloggs Cave (Australia), and on its implications for the knowledge of the timing and causes of Late Pleistocene extinctions of Australian megafauna, is published by David et al. (2021).[251]
- A study aiming to determine whether a significant relationship can be detected between demographic susceptibility to extinction of members of Quaternary megafauna of Sahul and their extinction chronology inferred from their fossil record is published by Bradshaw et al. (2021).[252]
- A study aiming to determine whether the fossil record indicates that the arrival of hominins on islands in the Pleistocene was coincident with the disappearance of insular taxa is published by Louys et al. (2021).[253]
- A study aiming to determine how observed extinctions in the geological past can be predicted from the interaction of long-term temperature trends with short-term climate change is published by Mathes et al. (2021).[254]
- A study on the impact of the Capitanian mass extinction event, Permian–Triassic extinction event and Triassic–Jurassic extinction event on terrestrial and freshwater ecosystems, aiming to quantify community resistance during the extinction events and to determine ecological dynamics of communities before and after these extinctions, is published by Huang et al. (2021).[255]
- A study on correlations between fossilization potential and food web features, aiming to determine how fossilization impacts inferences of ancient community structure, is published by Shaw et al. (2021).[256]
- A study on the drilling predation pressure on sea urchins across the Mesozoic and Cenozoic is published by Petsios et al. (2021), who present evidence indicative of the Cenozoic intensification of this predation, and argue that the Mesozoic marine revolution was more likely a series of asynchronous processes with variable significance across different groups of predators and preys, rather than a single synchronized ecosystem-wide event.[257]
- A study on the spatial biodiversity dynamics of unicellular marine plankton throughouth the Cenozoic, aiming to test the generality of the ‘out of the tropics’ hypothesis (positing that the tropics are both a cradle and source of biodiversity for extratropical regions), is published by Raja & Kiessling (2021).[258]
- A study on the evolution of ecophysiological adaptations to life in the sea in extant and fossil marine tetrapods (excluding birds) is published by Motani & Vermeij (2021).[259]
Other research
- Mißbach et al. (2021) report the existence of indigenous organic molecules and gases in primary fluid inclusions in c. 3.5-billion-year-old barites from the Dresser Formation (Pilbara Craton, Australia), providing evidence of the organic composition of primordial fluids that were available for the early microbes.[260]
- A study on the 3.4-billion-year old organic films from the Buck Reef Chert (Kaapvaal Craton, South Africa) is published by Alleon et al. (2021), who interpret their findings as indicating that early Archean organic films carry chemical information directly related to their original molecular compositions, and evaluate the implications of their finding for the knowledge of the initial chemical nature of organic microfossils found in ancient rocks.[261]
- Evidence of prolonged and repeated oxygen stress in the Appalachian Basin associated with the Late Devonian extinctions is presented by Boyer et al. (2021).[262]
- Rakociński et al. (2021) report very large anomalous mercury spikes from the south-western part of Tian Shan (Uzbekistan), and interpret this finding as evidence of intensive volcanic activity both predating and occurring during the Hangenberg Crisis.[263]
- Evidence from the southern Karoo Basin of South Africa indicative of at least four atmospheric carbon dioxide spikes coinciding with extinctions on land and at sea from the Late Permian to the Middle Triassic is presented by Retallack (2021).[264]
- A study evaluating whether fuel-driven changes to fire activity during the Cretaceous period had the ability to counteract rising atmospheric oxygen at this time is published by Belcher et al. (2021), who argue that alteration of fire feedbacks driven by the rise of the flowering plants likely lowered atmospheric oxygen levels from ~30% to 25% by the end of the Cretaceous.[265]
- White & Campione (2021) describe a workflow in which three-dimensional surface profiles of fragmentary fossils can be quantitatively compared to better-known exemplars in order to identify fragmentary fossils, and apply this workflow to megaraptorid theropod unguals from the Cretaceous of Australia.[266]
- A study aiming to test whether histological characters can be used to assign bones to individuals within a quarry, using sauropod dinosaur material from two adjacent Morrison quarries in the Bighorn Basin (Wyoming, United States) as a case study, is published by Wiersma-Weyand et al. (2021).[267]
- A study on diverse amniotic eggshells from the Wido Volcanics (Upper Cretaceous, South Korea), evaluating their utility for assessments of the paleothermometry of the sedimentary deposits, is published by Choi et al. (2021).[268]
- A study on the age and duration of the Lower Cretaceous Yixian Formation (China) is published by Zhong et al. (2021).[269]
- Goderis et al. (2021) report new data revealing a positive iridium anomaly within the peak-ring sequence of the Chicxulub impact structure, and interpret this finding as conclusively tying Chicxulub to the global iridium layer and Cretaceous-Paleogene boundary sections worldwide, confirming the link between crater formation and the iridium peak detected in these sections.[270]
- A study aiming to determine whether a strong link can be established between stable carbon isotopes of tooth enamel of herbivores and vegetation structure in present African ecosystems, and whether enamel stable carbon isotopes of fossil herbivores are useful for making inferences about Plio-Pleistocene vegetation structure in Africa and the environmental context of hominin evolution, is published by Robinson et al. (2021).[271]
- A study on environmental changes in East Africa at the time of the extinction of Paranthropus boisei is published by Quinn & Lepre (2021), who report evidence of a significant reduction in C4 grasslands during Mid-Pleistocene Transition, and argue that this reduction might have escalated dietary competition amongst the abundant C4-feeders and influenced P. boisei’s demise.[272]
- Evidence from Chitimwe Beds (northern Malawi), indicating that in the late Pleistocene early modern humans fundamentally altered local landscapes and ecology using fire, is presented by Thompson et al. (2021).[273]
- Ellis et al. (2021) examine current biodiversity patterns in relation to distribution of human populations and land use over the past 12,000 years, and argue that as early as 12,000 years ago nearly three quarters of Earth’s land was inhabited and shaped by human societies.[274]
- Alleon et al. (2021) revise reports of organic molecules in animal fossils, and argue that purported signatures of organic molecules are in reality instrumental artefacts resulting from intense background luminescence.[275]
Paleoclimate
- Scotese et al. (2021) estimate how global temperatures have changed during the last 540 million years.[276]
- A high-resolution proxy record of Late Cambrian and Ordovician climate is presented by Goldberg et al. (2021).[277]
- A study on the atmospheric CO2 levels during the Permian–Triassic transition, based on data from fossil plant remains from sedimentary successions in southwestern China, is published by Wu et al. (2021), who present evidence of a six-fold increase of atmospheric pCO2 during the Permian–Triassic mass extinction.[278]
- A study on the climate of the Lufeng area (China) during the Early Jurassic, and on the relationship between the global distribution of dinosaur fossils and climate during the Jurassic, is published by Shen et al. (2021).[279]
- Evidence of the presence of a terrestrial climate barrier in the Western Interior Basin of North America during the final 15 million years of the Cretaceous, dividing the Western Interior Basin into warm southern and cool northern biomes, is presented by Burgener et al. (2021), who also report evidence indicating that the biogeographical distribution of plants was heavily influenced by the presence of this temperature transition zone.[280]
- A study on CO2 contents of early Deccan Traps lavas, aiming to determine whether early Deccan magmatism triggered the warming event during the latest Maastrichtian, is published by Hernandez Nava et al. (2021).[281]
- Vento et al. (2021) estimate parameters of the Paleogene to Neogene climate on the basis of data from fossil leaves from the Río Turbio and Río Guillermo formations in southern South America (Argentina).[282]
- 10-million-year long proxy record of Arabian climate is developed by Böhme et al. (2021), who report evidence indicative of a sustained period of hyperaridity in the Pliocene and a number of transient periods of hyperaridity in northern Arabia during the late Miocene which were out of phase with those in North Africa, and argue that these desert dynamics had a strong control on large-scale mammalian dispersals between Africa and Eurasia.[283]
- A study aiming to reconstruct summer and winter temperatures in the Late Pleistocene when Neanderthals were using the site of La Ferrassie (France), based on data from oxygen isotope measurements of bovid tooth enamel, is published by Pederzani et al. (2021).[284]
- Data from analyses and modelling of noble gases in groundwater, indicating that the low-altitude, low-to-mid-latitude land surface (45 degrees south to 35 degrees north) was about 6 °C cooler during the Last Glacial Maximum than during the Late Holocene, is presented by Seltzer et al. (2021).[285]
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- ^ a b Gale, A. S. (2021). "The thoracican cirripede genus Concinnalepas Gale, 2014 (Crustacea) from the Middle and Upper Jurassic of southern England and northern France". Proceedings of the Geologists' Association. in press. doi:10.1016/j.pgeola.2021.01.007.
- ^ Tang, H. Y.; Mychko, E. V.; Feldmann, R. M.; Schweitzer, C. E.; Shaari, H.; Sone, M. (2021). "Malayacyclus gen. nov., the first Southeast Asian Cyclida (Crustacea) from the Early Carboniferous of Terengganu, Malaysia". Geological Journal. in press. doi:10.1002/gj.4128.
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: CS1 maint: unflagged free DOI (link) - ^ Matzke-Karasz, R.; Smith, R. J. (2021). "Temporal shifts in ostracode sexual dimorphism from the Late Cretaceous to the late Eocene of the U.S. Coastal Plain". Marine Micropaleontology. in press: Article 101959. doi:10.1016/j.marmicro.2020.101959.
- ^ Wernette, S. J.; Hughes, N. C.; Myrow, P. M.; Aung, A. K. (2021). "The first systematic description of Cambrian fossils from Myanmar: Late Furongian trilobites from the southern part of the Shan State and the early Palaeozoic palaeogeographical affinities of Sibumasu". Journal of Asian Earth Sciences. 214: Article 104775. doi:10.1016/j.jseaes.2021.104775.
- ^ a b c van Viersen, A. P. (2021). "Type and other species of Gerastos and allied genera (Trilobita, Proetinae) from the Siluro-Devonian". Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen. 299 (2): 185–217. doi:10.1127/njgpa/2021/0964.
- ^ a b Peel, J. S. (2021). "Trilobite fauna of the Telt Bugt Formation (Cambrian Series 2–Miaolingian Series), western North Greenland (Laurentia)". Bulletin of the Geological Society of Denmark. 69: 1–33. doi:10.37570/bgsd-2021-69-01.
- ^ Peel, J. S. (2021). "Eldoradia and Acrocephalops (Trilobita: Bolaspididae) from the middle Cambrian (Miaolingian) of northern Greenland (Laurentia)". GFF. 143 (1): 8–15. doi:10.1080/11035897.2020.1865446.
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- ^ Sun, Z.; Zeng, H.; Zhao, F. (2021). "Digestive structures in Cambrian Miaolingian trilobites from Shandong, North China". Acta Palaeontologica Sinica. 60 (1): 166–175. doi:10.19800/j.cnki.aps.2020024.
- ^ Hou, J.; Hughes, N. C.; Hopkins, M. J. (2021). "The trilobite upper limb branch is a well-developed gill". Science Advances. 7 (14): eabe7377. doi:10.1126/sciadv.abe7377. PMC 8011964. PMID 33789898.
- ^ Bicknell, R. D. C.; Holmes, J. D.; Edgecombe, G. D.; Losso, S. R.; Ortega-Hernández, J.; Wroe, S.; Paterson, J. R. (2021). "Biomechanical analyses of Cambrian euarthropod limbs reveal their effectiveness in mastication and durophagy". Proceedings of the Royal Society B: Biological Sciences. 288 (1943): Article ID 20202075. doi:10.1098/rspb.2020.2075. PMC 7893260. PMID 33499790.
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- ^ Dai, T.; Hughes, N. C.; Zhang, X.; Peng, S. (2021). "Development of the early Cambrian oryctocephalid trilobite Oryctocarella duyunensis from western Hunan, China". Journal of Paleontology. in press: 1–16. doi:10.1017/jpa.2020.111.
- ^ Bault, V.; Crônier, C.; Allaire, N.; Monnet, C. (2021). "Trilobite biodiversity trends in the Devonian of North Africa". Palaeogeography, Palaeoclimatology, Palaeoecology. 565: Article 110208. doi:10.1016/j.palaeo.2020.110208.
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