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2018 in paleontology

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), List of years (table)
palynomorphs and chemical residues. Because humans have encountered fossils for millennia, paleontology has a long in
history both before and after becoming formalized as a science. This article records significant discoveries and events paleontology
related to paleontology that occurred or were published in the year 2018. … 2008 · 2009 · 2010 · 2011 · 2012
· 2013 · 2014
· 2015 · 2016 · 2017 · 2018 · 2019 ·
Contents 2020 · 2021
· 2022 · 2023 · 2024 · 2025 · 2026 ·
Plants
2027 · 2028 …
Cnidarians
In science: 2015 · 2016 · 2017 ·
Research
2018 · 2019 · 2020 · 2021
New taxa
Art · Archaeology · Architecture ·
Arthropods Literature · Music · Philosophy ·
Bryozoans Science +...
New taxa
Brachiopods
Research
New taxa
Molluscs
Echinoderms
Conodonts
Research
New taxa
Fish
Amphibians
Research
New taxa
Lizards and snakes
Ichthyosauromorphs
Sauropterygians
Turtles
Extinct animals named in 2018
Archosauriformes
General research
Archosaurs
Other reptiles
Synapsids
Non-mammalian synapsids
Research
New taxa
Mammals
Other animals
Research
New taxa
Foraminifera
Research
New taxa
Other organisms
Research
New taxa
History of life in general
Other research
References

Plants

Cnidarians
Research
New three dimensionally phosphatized microfossils of coronate scyphozoan Qinscyphus necopinus, including a new type of fossil embryo, are
described from the Cambrian (Fortunian) Kuanchuanpu Formation (China) by Shao et al. (2018), who interpret their findings as indicating that
Qinscyphus underwent direct development.[2]
A study on the morphology of the conulariid species Carinachites spinatus based on a new specimen collected from the lower Cambrian
Kuanchuanpu Formation (China) is published by Han et al. (2018).[3]
Revision of stony corals from the Lower Cretaceous (Berriasian) Oehrli Formation (Austria and Switzerland) is published by Baron-Szabo
(2018), who compares this fauna with five additional Berriasian coral faunas.[4]

New taxa
Name Novelty Status Authors Age Type locality

Berezovsky &
Acropora incogtita[5] Sp. nov Valid Eocene
Satanovska

Actinoseris Gameil, El-Sorogy & Late Cretaceous


Sp. nov Valid Aruma Formation
riyadhensis[6] Al-Kahtany (Campanian)

Antheria fedorowskii[7] Sp. nov Valid Wang, Gorgij & Yao Late Carboniferous

Antheria robusta[7] Sp. nov Valid Wang, Gorgij & Yao Late Carboniferous

Gameil, El-Sorogy & Late Cretaceous


Asteroseris arabica[6] Sp. nov Valid Aruma Formation
Al-Kahtany (Campanian)

Astraraeatrochus[8] Gen. et sp. nov Valid Löser & Heinrich Late Cretaceous

Ricci, Lathuilière &


Astreoidogyra[9] Gen. et sp. nov Valid Late Jurassic
Rusciadelli

Król, Zapalski &


Aulocystis wendti[10] Sp. nov Valid Devonian (Emsian) Amerboh Group
Berkowski

Bainbridgia Król, Zapalski &


Sp. nov Valid Devonian (Emsian) Kess-Kess Formation
bipartita[10] Berkowski

Cambrorhytium
Sp. nov Valid Chang et al. Early Cambrian
gracilis[11]

Caryophyllia
(Caryophyllia) Sp. nov Valid Niko Miocene Bihoku Group
imamurai[12]

Catenipora Beiguoshan
Sp. nov Valid Liang, Elias & Lee Ordovician (Katian)
jingyangensis[13] Formation

Catenipora Beiguoshan
Sp. nov Valid Liang, Elias & Lee Ordovician (Katian)
tiewadianensis[13] Formation

Catenipora
Sp. nov Valid Liang, Elias & Lee Ordovician (Sandbian) Jinghe Formation
tongchuanensis[13]

Sp. nov Valid Late Jurassic


Clausastrea Ricci, Lathuilière &
eliasovae[9] Rusciadelli

Crinopora ireneae[8] Sp. nov Valid Löser & Heinrich Late Cretaceous

Crinopora thomasi[8] Sp. nov Valid Löser & Heinrich Late Cretaceous

Cunnolites
Gameil, El-Sorogy & Late Cretaceous
(Plesiocunnolites) Sp. nov Valid Aruma Formation
Al-Kahtany (Campanian)
riyadhensis[6]

Deltocyathoides
Sp. nov Valid Niko Miocene Bihoku Group
bihokuensis[12]

Fuchungopora Devonian
Sp. nov Valid Liang et al. Etoucun Formation
huilongensis[14] (Famennian)

Gen. et sp. et comb.


Geroastrea[8] Valid Löser & Heinrich Late Cretaceous
nov

Gosaviaraea
Sp. nov Valid Löser & Heinrich Late Cretaceous
aimeae[8]

Löser, Steuber & Late Cretaceous


Kozaniastrea[15] Gen. et sp. nov Valid
Löser (Cenomanian)

Lithophyllon Berezovsky &


Sp. nov Valid Eocene
comptus[16] Satanovska

Rodríguez, Schönlaub Carboniferous


Lonsdaleia carnica[17] Sp. nov Valid Kirchbach Formation
& Kabon (Mississippian)

Nefocoenia Sp. nov Valid Löser & Heinrich Late Cretaceous


seewaldi[8]
Nefocoenia werneri[8] Sp. nov Valid Löser & Heinrich Late Cretaceous

Neopilophyllia[18] Gen. et comb. nov Valid Wang in Wang et al. Silurian (Telychian) Ningqiang Formation

Oculina Berezovsky &


Sp. nov Valid Eocene
complanatis[19] Satanovska

Middle Triassic
Opolestraea[20] Gen. et comb. nov Valid Morycowa Karchowice Beds
(Anisian)

Gen. et sp. et comb.


Pachyheterocoenia[8] Valid Löser & Heinrich Late Cretaceous
nov

Pachyphylliopsis[8] Gen. et sp. nov Valid Löser & Heinrich Late Cretaceous

Paractinacis[8] Gen. et sp. nov Valid Löser & Heinrich Late Cretaceous
Löser, Steuber & Late Cretaceous
Plesiolites[15] Gen. et sp. nov Valid
Löser (Cenomanian)

Proplesiastraea
Sp. nov Valid Löser & Heinrich Late Cretaceous
rivkae[8]

Striatopora Król, Zapalski &


Sp. nov Valid Devonian (Emsian) Amerboh Group
marsupia[10] Berkowski

Löser, Steuber & Late Cretaceous


Styloheterocoenia[15] Gen. et 2 sp. nov Valid
Löser (Cenomanian)

Stylophora Niko, Suzuki &


Sp. nov Valid Miocene Katsuta Group
kibiensis[21] Taguchi

Sutherlandia
Sp. nov Valid Niko et al. Early Permian Jamal Formation
jamalensis[22]

Gen. et sp. et comb.


Synhydnophora[8] Valid Löser & Heinrich Late Cretaceous
nov

Wendticyathus[23] Gen. et sp. nov Valid Berkowski Devonian (Emsian)

Xystriphylloides
Sp. nov Valid Yu Early Devonian
distinctus[24]

Arthropods
Bryozoans

New taxa

Type
Name Novelty Status Authors Age
locality

Acanthodesia
Sp. nov Valid Di Martino & Taylor Holocene
variegata[25]

Calyptotheca
Sp. nov Valid Di Martino & Taylor Holocene
sidneyi[25]

Characodoma
Sp. nov Valid Di Martino & Taylor Holocene
wesselinghi[25]

Pleurocodonellina
Sp. nov Valid Di Martino & Taylor Early Pleistocene Pucangan Formation
javanensis[25]

Turbicellepora
Sp. nov Valid Di Martino & Taylor Holocene
yasuharai[25]

Brachiopods

Research
Studies on the ontogenetic development of early acrotretoid brachiopods based on well preserved specimens of the earliest Cambrian species
Eohadrotreta zhenbaensis and Eohadrotreta? zhujiahensis from the Shuijingtuo Formation (China) are published by Zhang et al. (2018).[26][27]
A study on the extinction and origination of members of the order Strophomenida during the Late Ordovician mass extinction is published by
Sclafani et al. (2018).[28]
A study on the body size of several brachiopod assemblages recorded into the extinction interval prior to the Toarcian turnover, collected from
representative localities around the Iberian Massif (Spain and Portugal), is published by García Joral, Baeza-Carratalá & Goy (2018).[29]

New taxa
Name Novelty Status Authors Age Type locality

Las Pl
Acrotreta calabozoi[30] Sp. nov Valid Lavié Ordovician (Sandbian)
Formation

Gaetani in Gaetani et
Adygella socotrana[31] Sp. nov Valid Middle Triassic
al.

Ahtiella famatiniana[32] Sp. nov Valid Benedetto Ordovician

Ahtiella tunaensis[32] Sp. nov Valid Benedetto Ordovician

Baeza-Carratalá,
Alebusirhynchia vorosi[33] Sp. nov Valid Early Jurassic
Dulai & Sandoval

Alekseevathyris[34] Gen. et sp. nov Valid Baranov & Blodgett Devonian (Givetian) Coronados Volca

Altaethyrella Hadabulaktag
Sp. nov Valid Sproat & Zhan Ordovician (late Katian)
tarimensis[35] Formation

Ambocoelia
Sp. nov Valid Zhang & Ma Devonian (Frasnian) Yidade Formation
yidadeensis[36]

Gretchishnikova in
Arpaspirifer[37][38] Gen. et comb. nov Valid Devonian (Famennian)
Alekseeva et al.

Alekseeva &
Devonian (Eifelian–
Aulacella finitima[37][38] Sp. nov Valid Gretchishnikova in
Givetian)
Alekseeva et al.

Biernatium sucoi[39] Sp. nov Valid García-Alcalde Devonian (Givetian) Portilla Formation

Benedetto, Lavie & Ordovician


Broggeria omaguaca[40] Sp. nov Valid
Muñoz (Tremadocian)

Churkinella[34] Gen. et sp. nov Valid Baranov & Blodgett Devonian (Givetian) Coronados Volca

Cingulodermis
Sp. nov Valid Mergl Devonian (Emsian)
pustulatus[41]
Coronadothyris[34] Gen. et sp. nov Valid Baranov & Blodgett Devonian (Givetian) Coronados Volca

Costisorthis lisae[39] Sp. nov Valid García-Alcalde Devonian (Givetian) Candás Formatio

Hongguleleng
Cyrtiorina houi[42] Sp. nov Valid Zong & Ma Devonian (Famennian)
Formation

Cyrtospirifer Afanasjeva in
Sp. nov Valid Devonian (Famennian)
dansikensis[37][38] Alekseeva et al.

Dalejina
Sp. nov Valid Mergl Devonian (Emsian)
aulacelliformis[41]

Datnella[43] Gen. et comb. nov Valid Baranov Early Devonian

Desquamatia globosa Baliński in Skompski Devonian (Givetian–


Subsp. nov Valid Szydłówek Beds
jozefkae[44] et al. Frasnian boundary)

Diazoma Oleneva in Alekseeva


Sp. nov Valid Devonian (Frasnian)
ghyumuschlugensis[37][38] et al.

Gretchishnikova in
Dichospirifer felixi[37][38] Sp. nov Valid Devonian (Famennian)
Alekseeva et al.

Eopholidostrophia
(Megapholidostrophia) Sp. nov Valid Strusz & Percival Silurian (Wenlock)
gigas[45]

Eressella[46] Gen. et comb. nov Valid Halamski & Baliński Middle Devonian

Alekseeva &
Devonian (Eifelian–
Gypidulina grandis[37][38] Sp. nov Valid Gretchishnikova in
Givetian)
Alekseeva et al.

Isorthis (Arcualla)
Sp. nov Valid Strusz & Percival Silurian (Wenlock)
delegatensis[45]

Jagtithyris[47] Gen. et comb. nov Valid Simon & Mottequin Late Cretaceous
(Maastrichtian)
Juxathyris Permian
Sp. nov Valid Wu et al. Changxing Forma
subcircularis[48] (Changhsingian)

Torres-Martínez,
Permian (Artinskian– Paso H
Kukulkanus[49] Gen. et sp. nov Valid Sour-Tovar &
Kungurian) Formation
Barragán

Leiochonetes Carboniferous
Sp. nov Valid Tazawa Hikoroichi Forma
onimarensis[50] (Mississippian)

Leptaena (Leptaena)
Sp. nov Valid Strusz & Percival Silurian (Wenlock)
australis[45]

Leurosina Afanasjeva, Jun-Ichi &


Sp. nov Valid Permian (Kungurian) Nabeyama Form
katasumiensis[51] Yukio

Torres-Martínez & Carboniferous


Martinezchaconia[52] Gen. et sp. nov Valid Ixtaltepec Forma
Sour-Tovar (Bashkirian-Moscovian)

Baeza-Carratalá,
Middle Triassic
Misunithyris[53] Gen. et sp. nov Valid Pérez-Valera & Pérez- Siles Formation
(Ladinian)
Valera

Morinorhynchus
Sp. nov Valid Strusz & Percival Silurian (Wenlock)
tucksoni[45]

Musalitinispira[43] Gen. et sp. nov Valid Baranov Early Devonian

Neochonetes
(Huangichonetes) Sp. nov Valid Tazawa & Araki Permian (Wordian) Kamiyasse Form
matsukawensis[54]

Newberria alaskensis[34] Sp. nov Valid Baranov & Blodgett Devonian (Givetian) Coronados Volca

Nucleospira
Sp. nov Valid Strusz & Percival Silurian (Wenlock)
quidongensis[45]
Opsiconidion bouceki[55] Sp. nov Valid Mergl, Frýda & Silurian (Ludfordian) Kopanina Format
Kubajko

Opsiconidion Mergl, Frýda &


Sp. nov Valid Silurian (Ludfordian) Kopanina Format
parephemerus[55] Kubajko

Pinguispirifer
Sp. nov Valid Mergl Devonian (Emsian)
kesskess[41]

Piridiorhynchus Khoshyeilagh
Sp. nov Valid Baranov et al. Devonian (Famennian)
jafariani[56] Formation

Pripyatispirifer Afanasjeva in
Sp. nov Valid Devonian (Frasnian)
caucasius[37][38] Alekseeva et al.

Punctospirifer Carboniferous
Sp. nov Valid Tazawa Hikoroichi Forma
iwatensis[50] (Mississippian)

Alekseeva &
Resserella Devonian (Emsian–
Sp. nov Valid Gretchishnikova in
dagnensis[37][38] Eifelian)
Alekseeva et al.

Reticulariopsis Oleneva in Alekseeva


Sp. nov Valid Devonian (Givetian)
rotunda[37][38] et al.

Alekseeva &
Rhipidomella
Sp. nov Valid Gretchishnikova in Devonian (Givetian)
arpensis[37][38]
Alekseeva et al.

Rugosochonetes Afanasjeva in Carboniferous


Sp. nov Valid
multistriatus[37][38] Alekseeva et al. (Tournaisian)

Freeman, Miller & Cambrian–Ordovician


Schizambon langei[57] Sp. nov Valid
Dattilo boundary

Alekseeva &
Devonian (Emsian–
Schizophoria lata[37][38] Sp. nov Valid Gretchishnikova in
Eifelian)
Alekseeva et al.

Alekseeva &
Schizophoria schnuri
Subsp. nov Valid Gretchishnikova in Devonian (Givetian)
altera[37][38]
Alekseeva et al.

Septatrypa tumulorum[58] Sp. nov Valid Baliński & Halamski Devonian (Emsian)

Alekseeva &
Devonian (Emsian–
Sieberella parva[37][38] Sp. nov Valid Gretchishnikova in
Eifelian)
Alekseeva et al.

Sp. nov Valid Devonian (Famennian)


Sphenospira Gretchishnikova in
dansikensis[37][38] Alekseeva et al.

Spinatrypina
(Spinatrypina) Sp. nov Valid Baranov Early Devonian
krivensis[43]

Afanasjeva in Devonian (Eifelian and


Spinocyrtia irinae[37][38] Sp. nov Valid
Alekseeva et al. Givetian)

Stenorhynchia ulrici[58] Sp. nov Valid Halamski & Baliński Devonian (Emsian)

Thomasaria Oleneva in Alekseeva


Sp. nov Valid Devonian (Eifelian)
caucasica[37][38] et al.

Trigonatrypa drotae[41] Sp. nov Valid Mergl Devonian (Emsian)

Undispirifer Oleneva in Alekseeva


Sp. nov Valid Devonian (Eifelian)
dansikensis[37][38] et al.

Afanasjeva in Carboniferous
Unispirifer arpensis[37][38] Sp. nov Valid
Alekseeva et al. (Tournaisian)

Zaigunrostrum
Sp. nov Valid Pakhnevich Devonian (Famennian)
nakhichevanense[59]

Zezinia[59] Gen. et sp. nov Valid Pakhnevich Devonian (Frasnian)

Molluscs

Echinoderms

Conodonts

Research
A study testing the proposed models of growth of conodont elements is published by Shirley et al. (2018).[60]
A study on the histological sections of Ordovician and Permian conodont dental elements from the Bell Canyon Formation (Texas, United
States), Harding Sandstone (Colorado, United States), Ali Bashi Formation (Iran) and Canadian Arctic, examining those fossils for the presence
and distribution of soft tissue biomarkers, is published by Terrill, Henderson & Anderson (2018).[61]
A study evaluating the δ18O variation within a species-rich conodont assemblage from the Ordovician (Floian) Factory Cove Member of the
Shallow Bay Formation, Cow Head Group (western Newfoundland, Canada), as well as assessing the implications of these data for determining
the paleothermometry of ancient oceans and conodont ecologic models, is published by Wheeley et al. (2018).[62][63][64]
A study on the body size and diversity of Carnian conodonts from South China and their implications for inferring the biotic and environmental
changes during the Carnian Pluvial Event is published by Zhang et al. (2018).[65]
A study assessing the similarity of late Paleozoic to Triassic conodont faunas known from the Cache Creek Terrane (Canada) is published by
Golding (2018).[66]
Reconstruction of the multi-element apparatus of the Middle Triassic conodont from British Columbia (Canada) belonging to the Neogondolella
regalis group within the genus Neogondolella is presented by Golding (2018).[67]
Reconstruction of the number and arrangement of elements in the apparatus of Hindeodus parvus published by Zhang et al. (2017)[68] is
criticized by Agematsu, Golding & Orchard (2018);[69] Purnell et al. (2018) defend their original conclusions.[70]
A cluster of icriodontid conodonts belonging to the species Caudicriodus woschmidti, providing new information on the apparatus structure of
icriodontid conodonts, is described from the Lower Devonian sediments in southern Burgenland (Austria) by Suttner, Kido & Briguglio (2018).[71]
A study on the species belonging to the genus Neognathodus, evaluating whether previously defined morphotype groups are reliably distinct
from one another, is published by Zimmerman, Johnson & Polly (2018).[72]

New taxa
Name Novelty Status Authors Age Type locality

Ancyrogondolella
Sp. nov Valid Orchard Late Triassic (Norian) Pardonet Formation
diakowi[73]

Ancyrogondolella
Sp. nov Valid Orchard Late Triassic (Norian) Pardonet Formation
equalis[73]

Ancyrogondolella
Sp. nov Valid Orchard Late Triassic (Norian) Pardonet Formation
inequalis[73]

Ancyrogondolella?
Sp. nov Valid Orchard Late Triassic (Norian) Pardonet Formation
praespiculata[73]

Ancyrogondolella
Sp. nov Valid Orchard Late Triassic (Norian) Pardonet Formation
transformis[73]

Baltoniodus Carlorosi, Sarmiento Ordovician Santa Gertrudi


Sp. nov Valid
cooperi[74] & Heredia (Dapingian) Formation

Declinognathodus
Sp. nov Valid Hu, Qi & Nemyrovska Carboniferous
intermedius[75]

Declinognathodus
Sp. nov Valid Hu, Qi & Nemyrovska Carboniferous
tuberculosus[75]

Kılıç, Plasencia & Middle Triassic


Gedikella[76] Gen. et sp. nov Valid
Önder (Anisian)

Alba Formation
Gnathodus Sanz-López & Blanco- Carboniferous Aspe-Brousset
Sp. nov Valid
mirousei[77] Ferrera (Mississippian) Formation
Black Rock Limeston

Idiognathodus Atrasado Formation


Sp. nov Valid Hogancamp & Barrick Carboniferous
abdivitus[78] Eudora Shale

Idiognathodus Atrasado Formation


Sp. nov Valid Hogancamp & Barrick Carboniferous
centralis[78] Eudora Shale

Idiognathodus Atrasado Formation


Sp. nov Valid Hogancamp & Barrick Carboniferous
sweeti[78] Eudora Shale

Idiognathoides Carboniferous (early


Sp. nov Valid Frederick & Barrick Ladrones Limestone
chaagulootus[79] Pennsylvanian)

Kamuellerella Kılıç, Plasencia & Middle Triassic


Sp. nov Valid
rectangularis[76] Önder (Anisian)

Ketinella Kılıç, Plasencia & Middle Triassic


Sp. nov Valid
goermueshi[76] Önder (Anisian)
Magnigondolella[80] Gen. et 5 sp. et comb. Valid Golding & Orchard Middle Triassic Favret Formation
nov (Anisian) Toad Formation

Mesogondolella Permian
Sp. nov Valid Yuan, Zhang & Shen Selong Group
hendersoni[81] (Changhsingian)

Mockina? spinosa[73] Sp. nov Valid Orchard Late Triassic (Norian) Pardonet Formation

Neopolygnathus Devonian
Sp. nov Valid Hartenfels & Becker
fibula[82] (Famennian)

Maekawa in
Neospathodus
Sp. nov Valid Maekawa, Komatsu & Early Triassic Taho Formation
arcus[83]
Koike

Maekawa in
Novispathodus
Sp. nov Valid Maekawa, Komatsu & Early Triassic Taho Formation
shirokawai[83]
Koike

Maekawa in
Novispathodus
Sp. nov Valid Maekawa, Komatsu & Early Triassic Taho Formation
tahoensis[83]
Koike

‘Ozarkodina’?
Sp. nov Valid Lu et al. Devonian (Emsian) Ertang Formation
chenae[84]

‘Ozarkodina’?
Sp. nov Valid Lu et al. Devonian (Emsian) Ertang Formation
wuxuanensis[84]

Polygnathus Devonian (late


Narkiewicz & Ispena Formation
linguiformis Subsp. nov Valid Eifelian–middle
Königshof Si Phai Formation
saharicus[85] Givetian)

Polygnathus
Narkiewicz & Plum Brook Shale
linguiformis Subsp. nov Valid Devonian (Givetian)
Königshof Si Phai Formation
vietnamicus[85]

Polygnathus
Sp. nov Valid Lu et al. Devonian (Emsian) Ertang Formation
praeinversus[84]

Polygnathus rhenanus Narkiewicz & Candás Formation


Subsp. nov Valid Devonian (Givetian)
siphai[85] Königshof Si Phai Formation
Polygnathus xylus Subsp. nov Valid Narkiewicz & Devonian (Givetian) Si Phai Formation
bacbo[85] Königshof

Pseudognathodus Sanz-López, Blanco- Carboniferous


Sp. nov Valid Prestatyn Limestone
posadachaconae[86] Ferrera & Miller (Mississippian)

Pseudopolygnathus Devonian
Subsp. nov Valid Hartenfels & Becker
primus tafilensis[82] (Famennian)

Permian
Golding & Orchard in Copley Limestone
Pustulognathus[87] Gen. et 2 sp. nov Valid (Guadalupian to
Golding Horsefeed Formation
Lopingian)

Quadralella
Late Triassic
(Quadralella) Sp. nov Valid Zhang et al.
(Carnian)
postica[88]

Quadralella Late Triassic


Sp. nov Valid Zhang et al.
robusta[88] (Carnian)

Quadralella Late Triassic


Sp. nov Valid Zhang et al.
wignalli[88] (Carnian)

Quadralella Late Triassic


Sp. nov Valid Zhang et al.
yongningensis[88] (Carnian)

Ordovician
Scandodus choii[89] Sp. nov Valid Lee
(Darriwilian)

Sweetognathus Riepe Sprin


Sp. nov Valid Read & Nestell Permian (Sakmarian)
duplex[90] Limestone

Sweetognathus Riepe Sprin


Sp. nov Valid Read & Nestell Permian (Sakmarian)
wardlawi[90] Limestone

Aboussalam & Becker


"Tortodus" sparlingi[91] Sp. nov Valid Devonian (Givetian)
in Brett et al.

Henryhouse
Formation
Walliserognathus[92] Gen. et comb. nov Valid Corradini & Corriga Silurian (Ludlow)
Roberts Mountain
Formation

Fish

Amphibians
Research
Evidence from multi-stable isotope data indicating that some Devonian vertebrates, including early tetrapods, were euryhaline and inhabited
aquatic environments subject to rapid changes in salinity is presented by Goedert et al. (2018).[93]
A study on the evolution of hindlimb musculature from the lobe-finned fishes to early tetrapods is published online by Molnar et al. (2018).[94]
A partial jaw resembling that of Crassigyrinus is described from the Tournaisian of Scotland by Clack, Porro & Bennett (2018), potentially
extending the existence of the genus by approximately 20 million years towards the base of the Carboniferous.[95]
A study on the fossil record of amphibians, aiming to identify traits that influenced the extinction risk of species, and using this data to predict the
extinction risk for living amphibian species, is published by Tietje & Rödel (2018).[96]
Description of anamniote tetrapod fossils from the Late Permian Sundyr Tetrapod Assemblage (Mari El, Russia) is published by Golubev &
Bulanov (2018).[97]
A study on the relationship between taxonomic and ecological diversity of temnospondyls across the Permian–Triassic boundary in the Karoo
Basin of South Africa is published by Tarailo (2018).[98]
A study on the morphology and phylogenetic relationships of Neldasaurus is published by Schoch (2018).[99]
A study on the morphological changes in the skull that have been considered related to size reduction in dissorophoids, evaluating whether
these changes are consistent with the consequences of miniaturization according to the studies in extant miniature amphibians, is published by
Pérez-Ben, Schoch & Báez (2018).[100]
A study on the phylogenetic relationships of dissorophoid temnospondyls, and on their relationship to modern amphibians, is published by
Schoch (2018), who names new taxon Amphibamiformes.[101]
Well-preserved postcranial skeletons of two dissorophids are described from the early Permian karst deposits near Richards Spur (Oklahoma,
United States) by Gee & Reisz (2018).[102]
A revision of the fossil material assigned to Fayella chickashaensis is published by Gee, Scott & Reisz (2018), who consider this species to be a
nomen dubium.[103]
Redescription of the holotype specimen of the dissorophid species Alegeinosaurus aphthitos is published by Gee (2018), who considers
Alegeinosaurus to be a junior synonym of Aspidosaurus.[104]
New skull remains of Cacops morrisi, as well as the first known postcranial remains of the taxon, are described from the Permian of the
Richards Spur locality (Oklahoma, United States) by Gee & Reisz (2018).[105]
Two new dissorophid specimens referred to Anakamacops petrolicus are described from the Guadalupian Dashankou Fauna of China by Liu
(2018).[106]
A study on the morphology and phylogenetic relationships of Limnogyrinus elegans is published by Schoch & Witzmann (2018).[107]
A study on the diversity of the morphology of the feeding system in stereospondyl temnospondyls is published by Penrice & Deeming
(2018).[108]
A study on the anatomy and phylogenetic relationships of Parotosuchus nasutus is published by Schoch (2018).[109]
A study on the morphology of specimens of Rhytidosteus from southeastern European Russia, and on their implications for inferring possible
feeding adaptations of this animal, is published by Sennikov & Novikov (2018).[110]
Partial mandible of a large-bodied metoposaurid is described from the Upper Triassic Chinle Formation exposures at Petrified Forest National
Park (Arizona, United States) by Gee & Parker (2018).[111]
Morphological description of two new small-bodied metoposaurid specimens from Petrified Forest National Park (Arizona, United States) and a
histological analysis of the vertebra of these specimens is published online by Gee & Parker (2018), who argue that their findings support the
interpretation of Apachesaurus as a juvenile metoposaurid.[112]
A small metoposaurid specimen interpreted as a juvenile specimen of Apachesaurus gregorii is described from the Petrified Forest National
Park (Arizona, United States) by Rinehart & Lucas (2018).[113]
A study on the histology of the humeri of members of the species Metoposaurus krasiejowensis, revealing the occurrence of two different
growth patterns (histotypes), is published by Teschner, Sander & Konietzko-Meier (2018).[114]
A study on the feeding mode of Metoposaurus krasiejowensis as indicated by bone microstructure and computational biomechanics is published
by Konietzko-Meier et al. (2018).[115]
Description of the ornamentation of clavicles and skull bones of Metoposaurus krasiejowensis is published by Antczak & Bodzioch (2018).[116]
Redescription of Regalerpeton weichangensis based on eight new specimens and a study on the phylogenetic relationships of the species is
published by Rong (2018).[117]
An incomplete vertebra of a member of Caudata is described from the Algerian part of the Cretaceous Kem Kem Beds by Alloul et al.
(2018).[118]
Description of bone anomalies in specimens of the cryptobranchid Eoscapherpeton asiaticum from the Upper Cretaceous Bissekty Formation
(Uzbekistan) and a study on their possible origin is published by Skutschas et al. (2018).[119]
A study on the life history of the cryptobranchid Aviturus exsecratus from the Paleocene of Mongolia is published online by Skutschas et al.
(2018).[120]
Description of new specimens of the fossil salamandrids Taricha oligocenica and Taricha lindoei from the Oligocene of Oregon, providing new
information on the morphology of these taxa, and a study on the phylogenetic relationships of these species is published by Jacisin & Hopkins
(2018).[121]
Cretaceous frog tracks are described from the Saok Island (South Korea) by Park et al. (2018), who name a new ichnotaxon Ranipes
saokensis.[122]
Fossils of members of the genus Palaeobatrachus are described from the Miocene (Turolian) localities in Adygea (Russia) by Syromyatnikova
(2018).[123]
A redescription and a study of the phylogenetic relationships of Baurubatrachus pricei is published by Báez & Gómez (2018).[124]
A redescription and a study of the phylogenetic relationships of Eorubeta nevadensis is published by Henrici et al. (2018).[125]
Description of new fossil material of Thaumastosaurus from three localities in Switzerland, and a revision of the stratigraphic records of the
genus Thaumastosaurus and other ranoid fossils from the Eocene of Europe, is published by Vasilyan (2018).[126]
A study on the skull morphology of Enosuchus breviceps is published by Bulanov & Golubev (2018).[127]
A study on the anatomy of regenerating tails in two specimens of the Carboniferous lepospondyl Microbrachis pelikani, comparing tail
regeneration in this taxon and in extant seal salamander and Ocoee salamander, is published by van der Vos, Witzmann & Fröbisch (2018).[128]
A study on the skull ornamentation of a large specimen of Brachydectes newberryi from Linton (Ohio, United States) is published by Mann
(2018).[129]
Description of the anatomy of the skeleton of the chroniosuchian species Bystrowiella schumanni and a study on the phylogenetic relationships
of chroniosuchians is published by Witzmann & Schoch (2018).[130]
A study on the variation of digit proportions and trackway parameters in diadectomorph tracks with a relatively short pedal digit V, representing
ichnogenus Ichniotherium, is published by Buchwitz & Voight (2018).[131]

New taxa
Name Novelty Status Authors Age Type locality

Carboniferous
Andersonerpeton[132] Gen. et comb. nov Valid Pardo & Mann Joggins Formation
(Bashkirian)

Late Cretaceous
Electrorana[133] Gen. et sp. nov Valid Xing et al. Burmese amber
(Cenomanian)

Enosuchus
Sp. nov Valid Bulanov & Golubev Late Permian
alveolatus[134]

Kitiakia[134] Gen. et sp. nov Valid Bulanov & Golubev Middle Permian Belebei Formation

Early Cretaceous
Kulgeriherpeton[135] Gen. et sp. nov Valid Skutschas et al. Batylykh Formation
(Berriasian–Barremian)

Permian–Triassic
Laosuchus[136] Gen. et sp. nov Valid Arbez, Sidor & Steyer Luang Prabang Basi
boundary

Syromyatnikova & Late Miocene (early


Latonia caucasica[137] Sp. nov Valid
Roček Turolian)

Mengbatrachus[138] Gen. et sp. nov Valid Tan et al. Early Cretaceous Longjiang Group

Carboniferous
Mesanerpeton[139] Gen. et sp. nov Valid Smithson & Clack Ballagan Formation
(Tournaisian)

Mioproteus
Sp. nov Valid Venczel & Codrea Early Oligocene
gardneri[140]

Permian
Nooxobeia[103] Gen. et sp. nov Valid Gee, Scott & Reisz
(Guadalupian?)

Early Cretaceous
Shirerpeton[141] Gen. et sp. nov Valid Matsumoto & Evans Kuwajima Formation
(Barremian)

Carboniferous (late
Tantallognathus[142] Gen. et sp. nov Valid Chen et al. Tournaisian or earliest Ballagan Formation
Viséan)
Tutusius[143] Gen. et sp. nov Valid Gess & Ahlberg Devonian (late Witpoort Formation
Famennian)

Devonian (late
Umzantsia[143] Gen. et sp. nov Valid Gess & Ahlberg Witpoort Formation
Famennian)

Lizards and snakes

Ichthyosauromorphs

Sauropterygians

Turtles

Archosauriformes

General research
A study on the diversification of archosauromorph reptiles from the middle Permian to the early Late Triassic is published by Ezcurra & Butler
(2018).[144]
A study on the phylogenetic relationships of phytosaurs is published by Jones & Butler (2018).[145]

Archosaurs

Other reptiles

Synapsids

Non-mammalian synapsids

Research
A description of the postcranial material referable to the caseid species Ennatosaurus tecton is published by Romano, Brocklehurst & Fröbisch
(2018).[146]
A study on the anatomy and phylogenetic relationships of Milosaurus mccordi is published by Brocklehurst & Fröbisch (2018).[147]
A skull of a juvenile specimen of Anteosaurus magnificus is described from the Permian Abrahamskraal Formation (South Africa) by Kruger,
Rubidge & Abdala (2018).[148]
A study on the evolution of the trigeminal nerve innervation in anomodonts is published by Benoit et al. (2018).[149]
A study on the stable oxygen and carbon isotope compositions of dentine apatite in the teeth of twenty-eight specimens of Diictodon feliceps,
and on their implications for inferring the potential role of climate in driving the late Capitanian mass extinction of terrestrial tetrapods, is
published by Rey et al. (2018).[150]
Description of the anatomy of six new skulls of the dicynodont Abajudon kaayai from the Permian (Guadalupian) lower Madumabisa Mudstone
Formation (Zambia) and a study on the phylogenetic relationships of the species is published by Olroyd, Sidor & Angielczyk (2018).[151]
A study on the anatomy of the bony labyrinth of the specimens of the dicynodont genus Endothiodon collected from the Permian K5 Formation
(Mozambique), comparing it with the closely related genus Niassodon, is published by Araújo et al. (2018).[152]
A study on the taphonomic history of a monotypic bonebed composed by several individuals attributable to the dicynodont Dinodontosaurus
collected in a classic Middle Triassic locality in Brazil, and on its implications for inferring possible gregarious behaviour in Dinodontosaurus, is
published online by Ugalde et al. (2018).[153]
Redescription of the dicynodont genus Sangusaurus and a study on its feeding system and phylogenetic relationships is published by
Angielczyk, Hancox & Nabavizadeh (2018).[154]
Partial hindlimb of a dicynodont nearing the size of Stahleckeria potens is described from the Triassic Lifua Member of the Manda Beds
(Tanzania) by Kammerer, Angielczyk & Nesbitt (2018), representing the largest dicynodont postcranial element from the Manda Beds reported
so far.[155]
Description of plant remains and palynomorphs preserved in the coprolites produced by large dicynodonts from the Triassic Chañares
Formation (Argentina), and a study on their implications for inferring the diet of dicynodonts, is published by Perez Loinaze et al. (2018).[156]
Tetrapod tracks, probably produced by dicynodonts, are described from the Upper Triassic Vera Formation of the Los Menucos Group
(Argentina) by Citton et al. (2018).[157]
A study on the age of putative Rhaetian dicynodont from Lipie Śląskie (Poland) is published online by Racki & Lucas (2018), who consider it
more likely that this dicynodont was of Norian age.[158]
A study on the anatomy of the skull of Cynariops robustus is published by Bendel et al. (2018).[159]
A study on rates of enamel development in a range of non-mammalian cynodont species, inferred from incremental markings, is published by
O'Meara, Dirks & Martinelli (2018).[160]
Description of the morphology of the skull of Cynosaurus suppostus and a study on the phylogenetic relationships of the species is published by
van den Brandt & Abdala (2018).[161]
Fossils of Cynognathus crateronotus are described for the first time from the Triassic Ntawere Formation (Zambia) and Manda Beds (Tanzania)
by Wynd et al. (2018).[162]
A study on the postcranial anatomy of a specimen of Diademodon tetragonus recovered from the Upper Omingonde Formation (Namibia) is
published by Gaetano, Mocke & Abdala (2018).[163]
Partial skull and postcranial skeleton of a member of the species Cricodon metabolus is described from the Triassic Ntawere Formation
(Zambia) by Sidor & Hopson (2018), who also study the phylogenetic relationships of members of the family Trirachodontidae.[164]
A study on the musculature, posture and range of motion of the forelimb of Massetognathus pascuali is published by Lai, Biewener & Pierce
(2018).[165]
New specimen of Trucidocynodon riograndensis, almost 20% larger than the holotype specimen, is described from the Carnian of Candelária
Sequence (southern Brazil) by Stefanello et al. (2018).[166]
Right dentary with teeth of Prozostrodon brasiliensis is described from the Late Triassic of Brazil by Pacheco et al. (2018), representing the
second known specimen of this species.[167]
Description of the anatomy of the postcranial skeleton of Prozostrodon brasiliensis is published by Guignard, Martinelli & Soares (2018).[168]
A study on the limb bone histology and life histories of Prozostrodon brasiliensis, Irajatherium hernandezi, Brasilodon quadrangularis and
Brasilitherium riograndensis is published by Botha-Brink, Bento Soares & Martinelli (2018).[169]
A study on the origin and relationships of ictidosaurian cynodonts, i.e. tritheledontids and therioherpetids, is published by Bonaparte & Crompton
(2018).[170]
A large (comprising at least 38 individuals) clutch of well-preserved perinates of Kayentatherium wellesi, found with a presumed maternal
skeleton, is described from the Lower Jurassic sediments of the Kayenta Formation (found on lands of the Navajo Nation) by Hoffman & Rowe
(2018);[171] in light of this finding, a new interpretation of earlier records of associations between adult and juvenile cynodonts is proposed by
Benoit (2019).[172]
Cynodont teeth (representing a brasilodontid and a Riograndia-like form) found in the Triassic locality in Brazil which also yielded the fossils of
Sacisaurus agudoensis are described by Marsola et al. (2018).[173]
A study on the evolution of the mammalian jaw is published by Lautenschlager et al. (2018), who find no evidence for a concurrent reduction in
jaw-joint stress and increase in bite force in key non-mammaliaform taxa in the cynodont–mammaliaform transition.[174]
Tetrapod burrows, likely produced by small eucynodonts, are described from the Triassic Chañares Formation (Argentina) by Fiorelli et al.
(2018).[175]
A study on the morphological diversity of vertebral regions in non-mammalian synapsids, and on its implication for elucidating the evolution of
anatomically distinct regions of the mammalian spines, is published by Jones et al. (2018).[176]
A study on teeth ontogeny in wide range of extinct synapsid lineages is published by LeBlanc et al. (2018), who interpret their findings as
indicating that the ligamentous tooth attachment system is not unique to crown mammals within Synapsida.[177]

New taxa
Name Novelty Status Authors Age Type locality

Chemnitz petrifie
Permian (Sakmarian- forest
Ascendonanus[178] Gen. et sp. nov Valid Spindler et al.
Artinskian transition) (Leukersdorf
Formation)

Lucas, Rinehart & Early Permian (early


Gordodon[179] Gen. et sp. nov Valid Bursum Formation
Celeskey Wolfcampian)

Gorynychus[180] Gen. et sp. nov Valid Kammerer & Masyutin Permian Kotelnich red beds

Tropidostoma
Permian (early
Leucocephalus[181] Gen. et sp. nov Valid Day et al. Assemblage Zone o
Wuchiapingian)
the Main Karoo Basin

Late Triassic (late


Lisowicia[182] Gen. et sp. nov Sulej & Niedźwiedzki Norian-earliest
Rhaetian)

Permian Abrahamskraal
Microvaranops[178] Gen. et sp. nov Valid Spindler et al.
(Guadalupian) Formation

Nochnitsa[183] Gen. et sp. nov Valid Kammerer & Masyutin Permian Kotelnich red beds

Pentasaurus[184] Gen. et sp. nov Valid Kammerer Late Triassic Elliot Formation

Late Triassic
Polonodon[185] Gen. et sp. nov Valid Sulej et al.
(Carnian)

Late Triassic (Carnian Santa Mari


Siriusgnathus[186] Gen. et sp. nov Valid Pavanatto et al.
or Norian[187]) Supersequence

Mammals
Other animals

Research
A review and synthesis of studies on the timing and environmental context of landmark events in early animal evolution is published by Sperling
& Stockey (2018).[188]
A study on the phylogenetic relationships of the rangeomorphs, dickinsoniomorphs and erniettomorphs as indicated by what is known of the
ontogeny of the rangeomorph Charnia masoni, dickinsoniomorph Dickinsonia costata and erniettomorph Pteridinium simplex is published by
Dunn, Liu & Donoghue (2018), who consider at least the rangeomorphs and dickinsoniomorphs to be metazoans.[189]
A study on the phylogenetic relationships of the rangeomorphs is published by Dececchi et al. (2018).[190]
A study on the size distribution and morphological features of a population of juvenile specimens of Dickinsonia costata from the Crisp Gorge
fossil locality in the Flinders Ranges (Australia) is published by Reid, García-Bellido & Gehling (2018).[191]
A study on the phylogenetic relationships of Dickinsonia based on data from lipid biomarkers extracted from organically preserved Ediacaran
macrofossils is published by Bobrovskiy et al. (2018), who interpret their findings as indicating that Dickinsonia was an animal.[192]
A study on the anatomy and phylogenetic relationships of Stromatoveris, based on data from new specimens from the Chengjiang Konservat‐
Lagerstätte (China), is published by Hoyal Cuthill & Han (2018), who interpret Stromatoveris as a member of early animal group Petalonamae
that also included Arborea, Pambikalbae, rangeomorphs, dickinsoniomorphs and erniettomorphs.[193]
The first reliable occurrence of abundant penetrative trace fossils, providing trace fossil evidence for Precambrian bilaterians with complex
behavioural patterns, is reported from the latest Ediacaran of western Mongolia by Oji et al. (2018).[194]
Trace fossils produced by Ediacaran animals which burrowed within sediment are described from the shallow-marine deposits of the Urusis
Formation (Nama Group, Namibia) by Buatois et al. (2018), who name a new ichnotaxon Parapsammichnites pretzeliformis.[195]
New trace fossils from the Ediacaran Shibantan Member of the upper Dengying Formation (China), including burrows and possible trackways
which were probably made by millimeter-sized animals with bilateral appendages, are described by Chen et al. (2018).[196]
An aggregation of members of the genus Parvancorina, providing evidence of two size-clusters and bimodal orientation in this taxon, is
described from the Ediacara Conservation Park (Australia) by Coutts et al. (2018).[197]
New, three-dimensional specimens of Charniodiscus arboreus (Arborea arborea), allowing for a detailed reinterpretation of its functional
morphology and taxonomy, are described from the Ediacara Member, Rawnsley Quartzite of South Australia by Laflamme, Gehling & Droser
(2018).[198]
3D reconstructions of Cloudina aggregates are presented by Mehra & Maloof (2018).[199]
A study on Namacalathus and Cloudina skeletons from the Ediacaran Omkyk Member of the Nama Group (Namibia) is published by Pruss et al.
(2018), who interpret their findings as indicating that both organisms originally produced aragonitic skeletons, which later underwent diagenetic
conversion to calcite.[200]
A study on the substrate growth dynamics, mode of biomineralization and possible affinities of Namapoikia rietoogensis is published by Wood &
Penny (2018).[201]
A review of evidence for existence of swimming animals during the Neoproterozoic is published by Gold (2018).[202]
A study on the age of the Cambrian Chengjiang biota (China) is published by Yang et al. (2018).[203]
Description of coprolites from the Cambrian (Drumian) Rockslide Formation (Mackenzie Mountains, Canada) produced by an unknown predator,
and a study on their implications for reconstructing the Cambrian food web, is published by Kimmig & Pratt (2018).[204]
A study on the nature and biological affinity of the Cambrian taxon Archaeooides is published by Yin et al. (2018), who interpret the fossils of
Archaeooides as embryonic remains of animals.[205]
Zumberge et al. (2018) report a new fossil sterane biomarker, possessing a rare hydrocarbon skeleton that is uniquely found within extant
demosponge taxa, from late Neoproterozoic–Cambrian sedimentary rocks and oils, and interpret this finding as indicating that demosponges,
and hence multicellular animals, were prominent in some late Neoproterozoic marine environments at least extending back to the Cryogenian
period.[206]
Diverse, abundant sponge fossils from the Ordovician–Silurian boundary interval are reported from seven localities in South China by Botting et
al. (2018), who produce a model for the distribution and preservation of the sponge fauna.[207]
A study on the phylogenetic relationships of extant and fossil demosponges is published by Schuster et al. (2018).[208]
An assemblage of animal fossils, including the oldest known pterobranchs, preserved in the form of small carbonaceous fossils is described
from the Cambrian Buen Formation (Greenland) by Slater et al. (2018).[209]
Description of new morphological features of the Cambrian mobergellan Discinella micans is published by Skovsted & Topper (2018).[210]
A study on the interrelationships between the eldonioid Pararotadiscus guizhouensis and associated fossil taxa from the Kaili Biota is published
by Zhao et al. (2018).[211]
A study on the slab with a dense aggregation of members of the species Banffia constricta recovered from the Cambrian Burgess Shale
(Canada) and its implications for life habits of the animal is published by Chambers & Brandt (2018).[212]
A study on the morphology and phylogenetic affinities of Yuyuanozoon magnificissimi, based on new specimens, is published by Li et al.
(2018).[213]
A study on the fossil record of early Paleozoic graptoloids and on the factors influencing rates of diversification within this group is published by
Foote et al. (2018).[214]
A study on the impact of the long-period astronomical cycles (Milankovitch “grand cycles”) associated with Earth's orbital eccentricity and
obliquity on the variance in species turnover probability (extinction probability plus speciation probability) in Early Paleozoic graptoloids is
published by Crampton et al. (2018).[215]
A redescription of the species Malongitubus kuangshanensis from the Cambrian Chengjiang Lagerstätte (China) is published by Hu et al.
(2018), who interpret this taxon as a pterobranch.[216]
A study on the morphology of the palaeoscolecid worm Palaeoscolex from the Lower Ordovician Fezouata Lagerstätte (Morocco), using
computed microtomography and providing new information on the internal anatomy of this animal, is published by Kouraiss et al. (2018).[217]
The first occurrence of the tommotiid species Paterimitra pyramidalis from the Xinji Formation (China) is reported by Pan et al. (2018).[218]
A study on the temporal distribution of lophotrochozoan skeletal species from the upper Ediacaran to the basal Miaolingian of the Siberian
Platform, and on its implications for understanding the evolutionary dynamics of the Cambrian explosion, is published by Zhuravlev & Wood
(2018).[219]
Eggs of ascaridoid nematodes found in crocodyliform coprolites are described from the Upper Cretaceous Bauru Group (Brazil) by Cardia et al.
(2018).[220]
A study reinterpreting the putative Cambrian lobopodian Mureropodia apae as a partial isolated appendage of a member of the genus
Caryosyntrips, published by Pates & Daley (2017)[221] is criticized by Gámez Vintaned & Zhuravlev (2018);[222] Pates, Daley & Ortega-
Hernández (2018) defend their original conclusions.[223]
A study on the early evolution of stem and crown-arthropods as indicated by Ediacaran and Cambrian body and trace fossils is published by
Daley et al. (2018).[224]
A study on the evolution of ecdysozoan vision, focusing on the evolution of arthropod multi-opsin vision, as indicated by molecular data and data
from fossil record, is published by Fleming et al. (2018).[225]
A juvenile specimen of Lyrarapax unguispinus, providing new information on the frontal appendages and feeding mode in this taxon, is
described from the Cambrian Chiungchussu Formation (China) by Liu et al. (2018).[226]
A study evaluating likely swimming efficiency and maneuverability of Anomalocaris canadensis is published by Sheppard, Rival & Caron
(2018).[227]
Cambrian animal Pahvantia hastata from the Wheeler Shale (Utah, United States), originally classified as a possible arthropod,[228] is
reinterpreted as a suspension-feeding radiodont by Lerosey-Aubril & Pates (2018).[229]
The presence of metameric midgut diverticulae is reported for the first time in the stem-arthropod Fuxianhuia protensa by Ortega-Hernández et
al. (2018), who interpret their finding as indicative of a predatory or scavenging ecology of fuxianhuiids.[230]
Liu et al. (2018) reinterpret putative remains of the nervous and cardiovascular systems in numerous articulated individuals of Fuxianhuia
protensa as more likely to be microbial biofilms that developed following decomposition of the intestine, muscle and other connective
tissues.[231]
A study on the post-embryonic development of Fuxianhuia protensa is published by Fu et al. (2018).[232]
Redescription of the fuxianhuiid Liangwangshania biloba is published by Chen et al. (2018).[233]
New specimens of the stem-arthropod species Kerygmachela kierkegaardi, providing new information on the anatomy of this species and on the
ancestral condition of the panarthropod brain, are described from the Cambrian Stage 3 of the Buen Formation (Sirius Passet, Greenland) by
Park et al. (2018).[234]
Fossils of spindle- or conotubular-shaped animals of uncertain phylogenetic placement are described from the Ordovician Martinsburg
Formation (Pennsylvania, United States) by Meyer et al. (2018).[235]
Evidence of macrofauna living at depths of up to 8 metres below the seabed is reported from the Permian Fort Brown Formation (Karoo Basin,
South Africa) by Cobain et al. (2018).[236]
A study on the morphology of the hyolithid Paramicrocornus zhenbaensis from the lower Cambrian Shuijingtuo Formation (China) is published
by Zhang, Skovsted & Zhang (2018), who report that this species lacked helens, and also report the oldest known hyolith muscle scars
preserved on the opercula of this species.[237]
A study on the feeding strategies and locomotion of Cambrian hyolithids, based on specimens preserved in coprolites from the Chengjiang biota
and associated with a Tuzoia carcass from the Balang Fauna (China), is published by Sun et al. (2018).[238]
Digestive tract of a specimen of the hyolith species Circotheca johnstrupi from the Cambrian Læså Formation (Bornholm, Denmark) is described
by Berg-Madsen, Valent & Ebbestad (2018).[239]
The oldest stromatoporoid–bryozoan reefs reported so far are described from the middle Ordovician Duwibong Formation (South Korea) by
Hong et al. (2018).[240]
Small bioconstructions formed solely by microconchid tube worms, representing the stratigraphically oldest exclusively metazoan
bioconstructions from the earliest Triassic (mid-Induan) strata in East Greenland, are reported by Zatoń et al. (2018).[241]
The oldest known evidence of trematode parasitism of bivalves in the form of igloo-shaped traces found on shells of the freshwater bivalve
Sphaerium is reported from the Upper Cretaceous Judith River Formation (Montana, United States) by Rogers et al. (2018).[242]
A study on the predatory drill holes in Late Cretaceous and Paleogene molluscan and serpulid worm prey from Seymour Island (Antarctica) and
their implications for inferring the effects of the Cretaceous–Paleogene extinction event on predator-prey dynamics at this site is published by
Harper, Crame & Sogot (2018).[243]
A study on burrows from Lower–Middle Triassic successions in South China assigned to the ichnotaxon Rhizocorallium, and on their
implications for inferring the course of biotic recovery following the Permian–Triassic extinction event, is published by Feng et al. (2018).[244]
A study evaluating how different species of fossil and extant free-living cupuladriid bryozoans responded to the environmental changes in the
Southwest Caribbean over the last 6 million years is published by O’Dea et al. (2018).[245]

New taxa
Name Novelty Status Authors Age Type locality

Acanthodesia
Sp. nov Valid Di Martino & Taylor Holocene
variegata[25]

Acoscinopleura Koromyslova, Martha Late Cretaceous (late


Sp. nov Valid
albaruthenica[246] & Pakhnevich Campanian)

Acoscinopleura Koromyslova, Martha Late Cretaceous


Sp. nov Valid
crassa[246] & Pakhnevich (Maastrichtian)

Acoscinopleura Koromyslova, Martha Late Cretaceous


Sp. nov Valid
dualis[246] & Pakhnevich (Maastrichtian)

Acoscinopleura Koromyslova, Martha Late Cretaceous


Sp. nov Valid
occulta[246] & Pakhnevich (Maastrichtian)

‘Aechmella’ Koromyslova,
Sp. nov Valid Late Cretaceous
viskovae[247] Baraboshkin & Martha

Aechmellina[248] Gen. et comb. nov Valid Taylor, Martha & Cretaceous


Gordon (Cenomanian) to
Paleocene (Danian).
Hongjingshao
Alacaris[249] Gen. et sp. nov Valid Yang et al. Cambrian Stage 3
Formation

Chengjiang
Allonnia nuda[250] Sp. nov Valid Cong et al. Cambrian Stage 3
Lagerstätte

Allonnia tenuis[251] Sp. nov Valid Zhao, Li & Selden Early Cambrian

Suárez Andrés &


Arnaopora[252] Gen. et sp. nov Valid Devonian Moniello Formation
Wyse Jackson

Aspidostoma Pérez, López-Gappa Monte Leó


Sp. nov Valid Early Miocene
armatum[253] & Griffin Formation

Aspidostoma Pérez, López-Gappa Puerto Madry


Sp. nov Valid Late Miocene
roveretoi[253] & Griffin Formation

Aspidostoma Pérez, López-Gappa Early to middle


Sp. nov Valid Chenque Formation
tehuelche[253] & Griffin Miocene

Austroscolex
Sp. nov Valid Liu et al. Cambrian (Paibian)
sinensis[254]

Paleocene (Danian) to
Axilosoecia[255] Gen. et 2 sp. nov Valid Taylor & Brezina Roca Formation
early Miocene

Burocratina[256] Gen. et sp. nov Wachtler & Ghidoni Early-Middle Triassic

Ordovician (late
Catenagraptus[257] Gen. et sp. nov Valid VandenBerg
Floian)

Characodoma Sp. nov Valid Di Martino & Taylor Holocene


wesselinghi[25]
Cheethamia Koromyslova,
Sp. nov Valid Late Cretaceous
aktolagayensis[247] Baraboshkin & Martha

Codositubulus[258] Gen. et sp. nov Valid Gámez Vintaned et al. Cambrian

Colospongia lenis[259] Sp. nov Valid Malysheva Late Permian

Cornulites Gutiérrez-Marco & Ordovician


Sp. nov Valid
gondwanensis[260] Vinn (Hirnantian)

Cupitheca
Sp. nov Valid Sun et al. Cambrian Manto Formation
convexa[261]

Ernst, Krainer & Carboniferous


Cystomeson[262] Gen. et sp. nov Valid Lake Valley Formatio
Lucas (Mississippian)

Decoritheca?
Sp. nov Valid Peel & Willman Cambrian Series 2 Buen Formation
hageni[263]

Demirastrites
Sp. nov Valid Štorch & Melchin Silurian (Aeronian)
campograptoides[264]

Dictyocyathus
Sp. nov Valid Perejón et al. Early Cambrian
aranosensis[265]

Didymograptellus
Sp. nov Valid Vandenberg Ordovician (Floian)
kremastus[266]

Erismacoscinus
Sp. nov Valid Perejón et al. Early Cambrian
ganigobisensis[265]

‘Escharoides’ Di Martino, Martha & Late Cretaceous


Sp. nov Valid
charbonnieri[267] Taylor (Maastrichtian)

Di Martino, Martha & Late Cretaceous


Fehiborypora[267] Gen. et comb. nov Valid
Taylor (Maastrichtian)

Gibbavasis[268] Gen. et sp. nov Vaziri, Majidifard & Ediacaran Kushk Series
Laflamme
Devonian (late
Homoctenus Ponta Gross
Sp. nov Valid Comniskey & Ghilardi Pragian or late
katzerii[269] Formation
Emsian)

Kalaallitia[263] Gen. et sp. nov Valid Peel & Willman Cambrian Series 2 Buen Formation

Late Cretaceous
Taylor, Martha &
Kamilocella[248] Gen. et comb. nov Valid (Cenomanian) to
Gordon
Campanian).

Gen. et sp. et comb. Dick, Sakamoto &


Kenocharixa[270] Valid Cretaceous to Eocene
nov Komatsu

Late Triassic
Khmeria minima[271] Sp. nov Valid Wendt
(Carnian)

Late Permian,
Khmeria
Sp. nov Valid Wendt possibly also
stolonifera[271]
Carboniferous

Vaziri, Majidifard &


Kimberella persii[268] Sp. nov Ediacaran Kushk Series
Laflamme

Kootenayscolex[272] Gen. et sp. nov Valid Nanglu & Caron Cambrian Burgess Shale

Laminacaris[273] Gen. et sp. nov Valid Guo et al. Cambrian Stage 3


Lenisambulatrix[275] Gen. et sp. nov Valid Ou & Mayer Cambrian Stage 3 Heilinpu Formation

Lunulites
Sp. nov Valid Hara et al. Eocene La Meseta Formation
marambionis[276]

Dick, Sakamoto & Late Cretaceous


Marginaria prolixa[270] Sp. nov Valid Himenoura Group
Komatsu (Campanian)

Ordovician
Matteolaspongia[277] Gen. et sp. nov Valid Botting, Zhang & Muir Wenchang Formation
(Hirnantian)

Chenque Formation
Melychocella Pérez, López-Gappa
Sp. nov Valid Early Miocene Monte Leó
biperforata[253] & Griffin
Formation

Micrascidites Sagular, Yümün &


Sp. nov Valid Quaternary
gothicus[278] Meriç

Micropora
Sp. nov Valid Hara et al. Eocene La Meseta Formation
nordenskjoeldi[276]

Carboniferous Agua de Luch


Minitaspongia[279] Gen. et sp. nov Valid Carrera et al.
(Tournaisian) Formation

Monniotia Sagular, Yümün &


Sp. nov Valid Quaternary
minutula[278] Meriç

Nasaaraqia[263] Gen. et sp. nov Valid Peel & Willman Cambrian Series 2 Buen Formation

Neotrematopora Tolokonnikova &


Sp. nov Valid Devonian (Frasnian) Lyaiol Formation
lyaoilensis[280] Ponomarenko

Nevadotheca
Sp. nov Valid Peel & Willman Cambrian Series 2 Buen Formation
boerglumensis[263]

Nidelric
Sp. nov Valid Zhao, Li & Selden Early Cambrian
gaoloufangensis[251]

Nogrobs Middle Jurassic


Sp. nov Valid Schlögl et al.
moroccensis[281] (Bajocian)

Otionellina Sp. nov Valid Hara et al. Eocene La Meseta Formation


antarctica[276]
Otionellina
Sp. nov Valid Hara et al. Eocene La Meseta Formation
eocenica[276]

Sun, Zhao & Zhu in


Pedunculotheca[282] Gen. et sp. nov Valid Cambrian Stage 3 Yu'anshan Formation
Sun et al.

‘Plagioecia’ Di Martino, Martha & Late Cretaceous


Sp. nov Valid
antanihodiensis[267] Taylor (Maastrichtian)

Platychelyna López-Gappa, Pérez Monte Leó


Sp. nov Valid Early Miocene
secunda[283] & Griffin Formation

Pleurocodonellina
Sp. nov Valid Di Martino & Taylor Early Pleistocene Pucangan Formation
javanensis[25]

Protohertzina Slater, Harvey & Cambrian Lontova Formation


Sp. nov Valid
compressa[284] Butterfield (Terreneuvian) Voosi Formation

Qinscolex[285] Gen. et sp. nov Valid Liu et al. Cambrian (Fortunian)

Ramskoeldia[286] Gen. et 2 sp. nov Valid Cong et al. Cambrian Maotianshan Shales

Reptomultisparsa Middle Jurassic


Sp. nov Valid Viskova & Pakhnevich
stratosa[287] (Callovian)

Rhagasostoma Late Cretaceous


Sp. nov Valid Koromyslova et al.
aralense[288] (Campanian)

Late Cretaceous
Rhagasostoma
Sp. nov Valid Koromyslova et al. (Turonian and
brydonei[288]
Coniacian)

Rhagasostoma Late Cretaceous


Sp. nov Valid Koromyslova et al.
operculatum[288] (Campanian)
Schistodictyon Sp. nov Valid Zhen Late Silurian
webbyi[289]

Cambrian
Seqineqia[290] Gen. et sp. nov Valid Peel Holm Dal Formation
(Guzhangian)

“Serpula” calannai[291] Sp. nov Valid Sanfilippo et al. Permian

“Serpula” prisca[291] Sp. nov Valid Sanfilippo et al. Permian

Shaanxiscolex[292] Gen. et sp. nov Valid Yang et al. Cambrian Stage 4

Shanscolex[285] Gen. et sp. nov Valid Liu et al. Cambrian (Fortunian)

Cambrian
Sisamatispongia[290] Gen. et sp. nov Valid Peel Holm Dal Formation
(Guzhangian)

Late Cretaceous (late


Kallankurichchi
Sonarina[293] Gen. et sp. nov Valid Taylor & Di Martino Campanian or early
Formation
Maastrichtian)

Pates, Daley & Stephen Formation


Stanleycaris[223] Gen. et sp. nov Valid Cambrian
Ortega-Hernández Wheeler Formation

Devonian (middle to Ponta Gross


Styliolina langenii[269] Sp. nov Valid Comniskey & Ghilardi
late Emsian) Formation

Sullulika[263] Gen. et sp. nov Valid Peel & Willman Cambrian Series 2 Buen Formation
Tallitaniqa[290] Gen. et sp. nov Valid Peel Cambrian Holm Dal Formation
(Guzhangian)

Henson Gletsche
Tarimspira artemi[295] Sp. nov Valid Peel Cambrian Stage 4
Formation

Devonian (late
Tentaculites Ponta Gross
Sp. nov Valid Comniskey & Ghilardi Pragian or late
kozlowskii[269] Formation
Emsian)

Devonian (late
Tentaculites Ponta Gross
Sp. nov Valid Comniskey & Ghilardi Pragian or late
paranaensis[269] Formation
Emsian)

Herefordshire
Thanahita[296] Gen. et sp. nov Siveter et al. Silurian (Wenlock
Lagerstätte

Trapezovitus
Sp. nov Valid Peel & Willman Cambrian Series 2 Buen Formation
malinkyi[263]

Turbicellepora
Sp. nov Valid Di Martino & Taylor Holocene
yasuharai[25]

Devonian (late
Ponta Gross
Uniconus ciguelii[269] Sp. nov Valid Comniskey & Ghilardi Pragian or late
Formation
Emsian)

Permian (Wordian) to San Cassian


Zardinisoma[271] Gen. et 5 sp. nov Valid Wendt
Triassic (Carnian) Formation

Zhijinites Cambrian
Sp. nov Valid Pan, Feng & Chang Yanjiahe Formation
tumourifomis[297] (Terreneuvian)

Foraminifera

Research
A study on the effects of differential ocean acidification at the Cretaceous-Paleocene transition on the planktonic foraminiferal assemblages
from the Farafra Oasis (Egypt) is published by Orabi et al. (2018).[298]
A wide variety of morphological abnormalities in planktic foraminiferal tests from the earliest Danian, mainly from Tunisian sections, is described
by Arenillas, Arz & Gilabert (2018).[299]
A study on the impact of the climatic and environmental perturbation on the morphology of foraminifera living during the Paleocene–Eocene
Thermal Maximum is published by Schmidt et al. (2018).[300]
Taxonomic compilation and partial revision of early Eocene deep-sea benthic Foraminifera is presented by Arreguín-Rodríguez et al. (2018).[301]
A study on the responses of two species of foraminifera (extant Truncorotalia crassaformis and extinct Globoconella puncticulata) to climate
change during the late Pliocene to earliest Pleistocene intensification of Northern Hemisphere glaciation (3.6–2.4 million years ago) is published
by Brombacher et al. (2018).[302]

New taxa
Name Novelty Status Authors Age Type locality

Alabamina heyae[303] Sp. nov Valid Fox et al. Oligocene

Dunghan Format
Langley Formatio
Lizard Sp
Formation
Navet Formation
Soldan, Petrizzo &
Alicantina[304] Gen. et comb. nov Valid Eocene Richmond Forma
Silva
Shaheed
Formation
Thebes Formatio
Universidad
Formation

Ammobaculites Hjalmarsdottir, Late Jurassic - Early Agardhfjellet


Sp. nov Valid
deflectus[305] Nakrem & Nagy Cretaceous Formation

Ammobaculites Hjalmarsdottir, Late Jurassic - Early Agardhfjellet


Sp. nov Valid
knorringensis[305] Nakrem & Nagy Cretaceous Formation

Ammobaculoides Kaminski, Malik & Middle Jurassic


Sp. nov Valid Dhruma Formatio
dhrumaensis[306] Setoyama (Bajocian)

Asterigerinella jonesi[307] Sp. nov Valid Rögl & Briguglio Miocene (Burdigalian) Quilon Formation

Brizalina keralensis[307] Sp. nov Valid Rögl & Briguglio Miocene (Burdigalian) Quilon Formation

Premec Fucek,
Chiloguembelina
Sp. nov Valid Hernitz Kucenjak & Eocene and Oligocene Cipero Formation
adriatica[308]
Huber

Premec Fucek,
Chiloguembelina Late Eocene and early
Sp. nov Valid Hernitz Kucenjak &
andreae[308] Oligocene
Huber

Ciperoella[309] Gen. et comb. nov Valid Olsson & Hemleben in Late Eocene to early Cipero Formation
Olsson et al. Miocene Tingnaro Formati
Colominella piriniae[310] Sp. nov Valid Mancin & Kaminski Pliocene

Cyclammina
Nom. nov Valid Hanagata Neogene
saidovae[311]

Dentoglobigerina Pearson, Wade &


Sp. nov Valid Eocene and Oligocene Navet Formation
eotripartita[312] Olsson in Wade et al.

Carboniferous (late Riepe S


Douglassites[313] Gen. et sp. nov Valid Read & Nestell
Pennsylvanian) Limestone

Late Cretaceous
Elazigina siderea[314] Sp. nov Valid Consorti & Rashidi Tarbur Formation
(Maastrichtian)

Globigerina Hemleben & Olsson in


Sp. nov Valid Oligocene Shubuta Formatio
archaeobulloides[315] Spezzaferri et al.

Globigerinella Spezzaferri & Coxall Oligocene, possibly


Sp. nov Valid
roeglina[315] in Spezzaferri et al. Miocene

Spezzaferri in
Globigerinoides joli[316] Sp. nov Valid Spezzaferri, Olsson & Miocene
Hemleben

Spezzaferri in
Globigerinoides
Sp. nov Valid Spezzaferri, Olsson & Miocene
neoparawoodi[316]
Hemleben

Globoconella
Sp. nov Valid Crundwell Early Pliocene
pseudospinosa[317]

Globorotaloides
Sp. nov Valid Spezzaferri & Coxall Oligocene and Miocene
atlanticus[318]

Globoturborotalita Sp. nov Valid Spezzaferri & Coxall Eocene to Miocene


eolabiacrassata[319] in Spezzaferri et al.
Globoturborotalita Olsson & Hemleben in
Sp. nov Valid Eocene and Oligocene
paracancellata[319] Spezzaferri et al.

Globoturborotalita Olsson & Hemleben in


Sp. nov Valid Oligocene and Miocene
pseudopraebulloides[319] Spezzaferri et al.

Haplophragmoides Hjalmarsdottir, Late Jurassic - Early Agardhfjellet


Sp. nov Valid
perlobatus[305] Nakrem & Nagy Cretaceous Formation

Hemisphaerammina
Sp. nov Valid McNeil & Neville Early Eocene
apta[320]

Early Cretaceous
Rigaud, Schlagintweit
Ichnusella senerae[321] Sp. nov Valid (Barremian–early
& Bucur
Aptian)

Labrospira Hjalmarsdottir, Late Jurassic - Early Agardhfjellet


Sp. nov Valid
lenticulata[305] Nakrem & Nagy Cretaceous Formation

Lenticulina stewarti[303] Sp. nov Valid Fox et al. Oligocene (Rupelian)

Early Cretaceous
Moulladella[322] Gen. et sp. nov Valid Bucur & Schlagintweit
(Valanginian-Barremian)

Schlagintweit & Late Cretaceous


Neodubrovnikella[323] Gen. et sp. nov Valid Tarbur Formation
Rashidi (Maastrichtian)

Neonavarella[324] Gen. et sp. nov Valid Giusberti, Kaminski & Paleocene (Thanetian) Scaglia R
Mancin Formation
Early Cretaceous
Neotrocholina Rigaud, Schlagintweit
Sp. nov Valid (Barremian–early
theodori[321] & Bucur
Aptian)

Late Oligocene to early


Nonion cepa[303] Sp. nov Valid Fox et al.
Miocene

Nummulites Al Menoufy &


Sp. nov Valid Eocene (Lutetian)
fayumensis[325] Boukhary

Nummulites Al Menoufy &


Sp. nov Valid Eocene (Lutetian)
tenuissimus[325] Boukhary

Omphalocyclus
Late Cretaceous
macroporus Subsp. nov Valid Al Nuaimy Aqra Formation
(Maastrichtian)
ellipsoides[326]

Omphalocyclus
Late Cretaceous
macroporus Subsp. nov Valid Al Nuaimy Aqra Formation
(Maastrichtian)
maukabensis[326]

Consorti,
Late Cretaceous
Palaeoelphidium[327] Gen. et comb. nov Valid Schlagintweit &
(Maastrichtian)
Rashidi

Paralachlanella[307] Gen. et sp. nov Valid Rögl & Briguglio Miocene (Burdigalian) Quilon Formation

Pseudomassilina
Sp. nov Valid Rögl & Briguglio Miocene (Burdigalian) Quilon Formation
quilonensis[307]

Consorti in Consorti et Late Cretaceous (late


Pseudopeneroplis[328] Gen. et sp. nov Valid
al. Cenomanian)

Coxall & Spezzaferri


Quiltyella[315] Gen. et comb. nov Valid Oligocene and Miocene
in Spezzaferri et al.

Ranikothalia daviesi[329] Sp. nov Valid Sirel & Deveciler Early Eocene
Reophax pyriloculus[305] Sp. nov Valid Hjalmarsdottir, Late Jurassic - Early Agardhfjellet
Nakrem & Nagy Cretaceous Formation

Villa in Villa, Merino- La Nueva Limesto


Schubertella Carboniferous
Sp. nov Valid Tomé & Martín Meruxalín Limest
luisorum[330] (Moscovian)
Llaneza Sutu Limestone

Streptochilus
Sp. nov Valid Smart & Thomas Oligocene
tasmanensis[331]

Olsson, Pearson & Late Eocene and


Subbotina projecta[332] Sp. nov Valid Yazoo Formation
Wade in Wade et al. Oligocene

Hjalmarsdottir, Late Jurassic - Early Agardhfjellet


Textularia pernana[305] Sp. nov Valid
Nakrem & Nagy Cretaceous Formation

Spezzaferri in
Trilobatus
Sp. nov Valid Spezzaferri, Olsson & Miocene
altospiralis[316]
Hemleben

Middle Jurassic (late


Trochammina
Sp. nov Valid Glinskikh & Nikitenko Bajocian-early Churkino Formati
jakovlevae[333]
Bathonian)

Uvigerina kingi[303] Sp. nov Valid Fox et al. Middle Miocene

Other organisms

Research
A study on putative stromatolites described from the 3,700-Myr-old rocks from the Isua supracrustal belt (Greenland) by Nutman et al.
(2016)[334] is published by Allwood et al. (2018), who interpret these putative stromatolites as more likely to be structures of non-biological
origin.[335]
Carbon isotope analyses of 11 microbial fossils from the ∼3,465-million-year-old Apex chert (Australia) are published by Schopf et al. (2018),
who interpret two of the five studied species as primitive photosynthesizers, one as an Archaeal methane producer, and two as methane
consumers.[336]
The oldest well-preserved microbial mats fabrics are described from the ≈3,472-million-year-old Middle Marker horizon, Barberton Greenstone
Belt (South Africa) by Hickman-Lewis et al. (2018).[337]
Direct fossil evidence for life on land 3,220 million years ago in the form of terrestrial microbial mats is reported from the Moodies Group (South
Africa) by Homann et al. (2018).[338]
Microfossils representing 18 morphotypes are reported from the c. 2.4 billion years old Turee Creek Group (Western Australia) by Barlow & Van
Kranendonk (2018).[339]
Ten representative types of exceptionally well‐preserved mat‐related structures, interpreted as likely to be of biological origin and including
putative microbial mats and discoidal microbial colonies, are reported from the 2.1‐billion‐year‐old Francevillian series in Gabon by Aubineau et
al. (2018).[340]
A study on the chemical, isotopic and molecular structural characteristics of the putative multicellular eukaryote fossils from carbonaceous
compressions in the 1.63 billion years old Tuanshanzi Formation (China) is published by Qu et al. (2018).[341]
Intact porphyrins, the molecular fossils of chlorophylls, are described from 1,100-million-year-old marine black shales of the Taoudeni Basin
(Mauritania) by Gueneli et al. (2018), who also study the nitrogen isotopic values of the fossil pigments, and interpret their findings as indicating
that the oceans of that time were dominated by cyanobacteria, while larger planktonic algae were scarce.[342]
A study on the evolutionary history of bacteria is published by Louca et al. (2018), who interpret their findings as indicating that most bacterial
lineages ever to have inhabited Earth are extinct.[343]
Bobrovskiy et al. (2018) report molecular fossils from organically preserved specimens of Beltanelliformis, and interpret the fossils as
representing large spherical colonies of cyanobacteria.[344]
Discoid imprints sampled from the Precambrian terranes of central Dobruja (Romania) are described and assigned to the species
Beltanelliformis brunsae by Saint Martin & Saint Martin (2018).[345]
A study on the age of the fossil red alga Bangiomorpha pubescens is published by Gibson et al. (2018).[346]
A reassessment of the anatomy and taxonomy of Orbisiana, based on a restudy of the rediscovered original type material of O. simplex, is
published by Kolesnikov et al. (2018).[347]
A study on the positions of fossil specimens in the assemblages of Ediacaran fossils from Mistaken Point (Canada), as well as on their
implications for inferring the interactions and associations between the Ediacaran organisms, is published by Mitchell & Butterfield (2018).[348]
A study on the height of Ediacaran organisms from Mistaken Point, evaluating the link between the increase of height and resource competition
or greater offspring dispersal, is published by Mitchell & Kenchington (2018).[349]
Evidence of a radiation of the Ediacaran biota that witnessed the emergence and widespread implementation of novel, animal-style ecologies is
presented by Tarhan et al. (2018), who argue that this transition was linked to the expansion of Ediacaran taxa into dynamic, shallow marine
environments characterized by episodic disturbance and complex and diverse organically-bound substrates, and propose that younger, second-
wave Ediacaran communities resulting from said radiation were part of an ecological and evolutionary continuum with Phanerozoic
ecosystems.[350]
A study on the size range, ontogeny and palaeoenvironment of Rugoconites is published by Hall, Droser & Gehling (2018).[351]
Elliptical body fossils are described from the Ediacaran–Fortunian deposits of central Brittany (France) by Néraudeau et al. (2018), representing
the first body fossils described from these deposits.[352]
A study on the sandstone- and limestone-hosted occurrences of Palaeopascichnus linearis (including material from a new locality in Arctic
Siberia), indicative of a greater range of taxonomic and taphonomic variation, is published by Kolesnikov et al. (2018).[353]
A study on the organic‐walled microfossils from the Cambrian strata in the stratotype section of the Precambrian–Cambrian boundary in the
Burin Peninsula (Canada) is published by Palacios et al. (2018).[354]
Fossils interpreted as threads of filamentous cyanobacteria are described from the Cambrian (Guzhangian) Alum Shale Formation (Sweden) by
Castellani et al. (2018).[355]
Enigmatic Devonian taxon Protonympha is interpreted as a possible post-Ediacaran vendobiont by Retallack (2018).[356]
Description of fossils of nonmarine diatoms belonging to the genus Actinocyclus from the Lower to Middle Miocene lacustrine deposits in Japan
and a study on the possible causal links between the evolution of nonmarine planktonic diatoms and the climatic and environmental changes
that occurred during the Miocene is published by Hayashi et al. (2018).[357]
A study on the cell-size frequency distributions across calcareous nanoplankton communities through the Paleocene–Eocene Thermal
Maximum, on their population biomass and on the impact of climate change on their cellular characteristics is published by Gibbs et al.
(2018).[358]

New taxa
Name Novelty Status Authors Age Type locality

Alievium
Sp. nov Valid Bragina & Bragin Late Cretaceous
mangalensiense[359]

Noetinger, di Pasquo
Angochitina plicata[360] Sp. nov Valid Devonian
& Starck

Anhuithrix[361] Gen. et comb. nov Pang et al. Tonian Liulaobei Format

Attenborites[362] Gen. et sp. nov In press Droser et al. Ediacaran Rawnsley Quartz

Rikkinen & Schmidt in


Chaenotheca succina[363] Sp. nov Valid Eocene (Priabonian) Baltic amber
Rikkinen et al.

Cyclotella cassandrae[364] Sp. nov Valid Paillès et al. Pleistocene

Cyclotella petenensis[364] Sp. nov Valid Paillès et al. Pleistocene

Hongjingshao
Doulia[365] Gen. et sp. nov Valid Lian et al. Cambrian Stage 3
Formation

Eolaminaria Hongjingshao
Sp. nov Valid Lian et al. Cambrian Stage 3
simigladiola[365] Formation

Epistacheoides Falahatgar, Vachard & Carboniferous


Sp. nov Valid
bozorgniai[366] Sarfi (Viséan)

Ekspedition
Girvanella lianiformis[367] Sp. nov Valid Peel Cambrian (Drumian)
Formation

Ekspedition
Girvanella pituutaq[367] Sp. nov Valid Peel Cambrian (Drumian)
Formation
Gorgonisphaeridium Sp. nov Valid Noetinger, di Pasquo Devonian
impexus[360] & Starck

Kenchington, Dunn &


Hylaecullulus[368] Gen. et sp. nov Valid Ediacaran
Wilby

Loron & Visingsö Group


Leiosphaeridia gorda[369] Sp. nov Valid Tonian
Moczydłowska Wynniatt Formati

Slater, Harvey & Cambrian


Lontohystrichosphaera[284] Gen. et sp. nov Valid Lontova Formatio
Butterfield (Terreneuvian)

Mallomonas aperturae[370] Sp. nov Valid Siver Middle Eocene Giraffe Pipe local

Mallomonas bakeri[371] Sp. nov Valid Siver Middle Eocene Giraffe Pipe local

Mallomonas skogstadii[371] Sp. nov Valid Siver Middle Eocene Giraffe Pipe local

Carboniferous
(Mississippian) to Late
Mispertonia[372] Gen. et sp. nov Valid McLean et al.
Permian or Early
Triassic

Obamus[373] Gen. et sp. nov In press Dzaugis et al. Ediacaran Rawnsley Quartz

Ekspedition
Orpikania[367] Gen. et sp. nov Valid Peel Cambrian (Drumian)
Formation

Riedman, Porter &


Pakupaku[374] Gen. et sp. nov Valid Tonian Black River Dolom
Calver
Palaeomycus[375] Gen. et sp. nov Valid Poinar Late Cretaceous Burmese amber
(Cenomanian)

Late Cretaceous
Paleoambrosia[376] Gen. et sp. nov Valid Poinar & Vega Burmese amber
(Cenomanian)

Krings, Harper &


Perexiflasca[377] Gen. et sp. nov Valid Devonian (Pragian) Rhynie chert
Taylor

Kaasalainen, Rikkinen
Phyllopsora magna[378] Sp. nov Valid & Schmidt in Miocene Dominican ambe
Kaasalainen et al.

Pierceites Late Cretaceous


Sp. nov Valid Prasad et al.
deccanensis[379] (Maastrichtian)

Pseudoalievium[359] Gen. et 2 sp. nov Valid Bragina & Bragin Late Cretaceous

Pseudoaulophacus
Sp. nov Valid Bragina & Bragin Late Cretaceous
decoratus[359]

Strullu-Derrien in
Retesporangicus[380] Gen. et sp. nov Valid Early Devonian Rhynie chert
Strullu-Derrien et al.

Slater, Harvey & Cambrian Lontova Formatio


Retiranus[284] Gen. et sp. nov Valid
Butterfield (Terreneuvian) Voosi Formation

Hongjingshao
Rugophyca[365] Gen. et sp. nov Valid Lian et al. Cambrian Stage 3
Formation
Saarinomorpha[381] Gen. et sp. nov Valid Kolosov & Sofroneeva Vendian

Hongjingshao
Singulariphyca[365] Gen. et sp. nov Valid Lian et al. Cambrian Stage 3
Formation

Stellarossica[382] Gen. et comb. nov Valid Vorob'eva & Sergeev Precambrian Ura Formation

Synsphaeridium
Sp. nov Valid Yin et al. Cambrian Series 3
parahioense[383]

Downton C
Tristratothallus[384] Gen. et sp. nov Valid Edwards et al. Silurian (Ludfordian)
Sandstone Forma

Vendotaenia Yang & Qin in Yang et


Sp. nov Valid Ediacaran Dengying Format
pavimentpes[385] al.

Yang & Qin in Yang et


Vendotaenia sixiense[385] Sp. nov Valid Ediacaran Dengying Format
al.

Late Pliocene to early


Vizellopsidites[386] Gen. et sp. nov Valid Khan, Bera & Bera Kimin Formation
Pleistocene

Windipila pumila[387] Sp. nov Valid Krings & Harper Early Devonian Rhynie chert

History of life in general


Research related to paleontology that concerns multiple groups of the organisms listed above.

A study on the history of life on Earth is published by McMahon & Parnell (2018), who argue that the subsurface “deep biosphere” outweighed
the surface biosphere by about one order of magnitude for at least half of the history of life.[388]
A timescale of life on Earth, based on a reappraisal of the fossil material and new molecular clock analyses, is presented by Betts et al.
(2018).[389]
A study on functional shifts in modern phototrophic microbial mats across redox gradients, and on its implications for inferring the metabolic
transitions experienced during the Great Oxygenation Event, is published by Gutiérrez-Preciado et al. (2018).[390]
A study on living cyanobacteria, testing the hypothesis that planktonic single-celled cyanobacteria could drive the export of organic carbon from
the surface to deep ocean in the Paleoproterozoic, is published by Kamennaya et al. (2018).[391]
A study on the abundance of bio-essential trace elements during the period in Earth's history known as the "Boring Billion" is published by
Mukherjee et al. (2018), who interpret their findings as incidacting that key biological innovations in eukaryote evolution (the appearance of first
eukaryotes, the acquisition of certain cell organelles, the origin of multicellularity and the origin of sexual reproduction) probably occurred during
the period of a scarcity of trace elements, followed by a broad-scale diversification of eukaryotes during the period of a relative abundance of
trace elements.[392]
A study on the eukaryotic species richness during Tonian and Cryogenian is published by Riedman & Sadler (2018).[393]
A study on the Ediacaran ecosystem complexity is published by Darroch, Laflamme & Wagner (2018), who report evidence of the Ediacara
biota forming complex-type communities throughout much of their stratigraphic range, and thus likely comprising species that competed for
different resources and/or created niche for others.[394]
A study evaluating how temperature can govern oxygen supply to animals at oceanographic scales, as well as how temperature dynamically
affects the absolute tolerance of partial pressure of oxygen in marine ectotherms, and re-examining bathymetric patterns within the Ediacaran
fossil record in an ecophysiological context, is published by Boag et al. (2018).[395]
A study investigating possible water column redox controls on the distribution and growth of the oldest animal communities, based on data from
the Ediacaran Nama Group (Namibia), is published by Wood et al. (2018).[396]
A study on the duration of the faunal transition from Ediacaran to Cambrian biota, as indicated by data from a composite section in Namibia, is
published online by Linnemann et al. (2018).[397]
A study on the evolution of the diversity of animal body plans, based on data from extant and Cambrian animals, is published by Deline et al.
(2018).[398]
A review of the evidence for shell crushing (durophagy), drilling and puncturing predation in the Cambrian (and possibly the Ediacaran) is
published by Bicknell & Paterson (2018).[399]
A study on the timing and process of ocean oxygenation in the early Cambrian and its impact on the diversification of early Cambrian animals,
based on data from the Cambrian Niutitang Formation (China), is published by Zhao et al. (2018).[400]
A study on the evolution of marine animal communities over the Phanerozoic, evaluating the ecological changes caused by major radiations and
mass extinctions, is published by Muscente et al. (2018).[401]
A study evaluating whether rapid warming preferentially increased the extinction risk of tropical marine fossil taxa throughout the Phanerozoic is
published online by Reddin, Kocsis & Kiessling (2018).[402]
A study on the impact of mass extinctions on the global biogeographical structure, as indicated by data on time-traceable bioregions for benthic
marine species across the Phanerozoic, is published by Kocsis, Reddin & Kiessling (2018).[403]
A study on the nektic and eunektic diversity and occurrences throughout the Paleozoic is published by Whalen & Briggs (2018).[404]
A study analyzing the link between net latitudinal range shifts of marine invertebrates and seawater temperature over the (post-Cambrian)
Phanerozoic Eon is published by Reddin, Kocsis & Kiessling (2018).[405]
A study on within-habitat, between-habitat, and overall diversity of benthic marine invertebrates (gastropods, bivalves, trilobites, brachiopods
and echinoderms) from Phanerozoic geological formations is published online by Hofmann, Tietje & Aberhan (2018).[406]
A study evaluating the link between macroevolutionary success (evolving many species) and macroecological success (the occupation of an
unusually high number of areas by a species or clade) in fossil echinoid, cephalopod, bivalve, gastropod, brachiopod and trilobite species is
published by Wagner, Plotnick & Lyons (2018).[407]
A study comparing the extinction events which occurred at the end of the Ordovician and at the end of the Capitanian (middle Permian) is
published by Isozaki & Servais (2018).[408]
Filamentous microorganisms associated with annelid tubeworms are described from the Ordovician to early Silurian Yaman Kasy volcanic-
hosted massive sulfide deposit (Ural Mountains, Russia) by Georgieva et al. (2018).[409]
A study on the Devonian strata in the Zachełmie Quarry (Poland) preserving tracks of early tetrapods is published by Qvarnström et al. (2018),
who reinterpret the tracks as produced in non-marine environment.[410]
Vertebrate fossil fauna from the Tournaisian-age Ballagan Formation exposed on the beach at Burnmouth (Scotland) is described by Otoo et al.
(2018).[411]
A study on the early tetrapod diversity and biogeography in the Carboniferous and early Permian, evaluating the impact of the Carboniferous
rainforest collapse on early tetrapod communities, is published by Dunne et al. (2018).[412]
A study on the patterns of dispersal and vicariance of tetrapods across Pangaea during the Carboniferous and Permian is published by
Brocklehurst et al. (2018).[413]
O’Connor et al. (2018) reconstruct the most likely karyotype of the diapsid common ancestor based on data from extant reptiles and birds, and
argue that most features of a typical ‘avian-like’ karyotype were in place before the divergence of birds and turtles ≈255 million years ago.[414]
A study evaluating whether the fossil record supports the reality of the Permian Olson's Extinction, based on an analysis of the tetrapod species
richness in the tetrapod-bearing formations of Texas preserving fossils from the time of the extinction, is published by Brocklehurst (2018).[415]
A study on the patterns of species richness, origination rates and extinction rates of the mid-Permian tetrapods from South Africa is published
by Day et al. (2018).[416]
A study on the changes of distribution of terrestrial tetrapods from the Permian (Guadalupian) to the Middle Triassic and on the impact of the
Permian–Triassic extinction event on the palaeobiogeography of terrestrial tetrapods is published by Bernardi, Petti & Benton (2018).[417]
A study on the causes of biotic extinction during the Guadalupian-Lopingian transition is published online by Huang et al. (2018).[418]
A study on the composition and biotic interactions in terrestrial paleocommunities from the Karoo Basin (South Africa) spanning the Permian-
Triassic mass extinction is published online by Roopnarine et al. (2018), who propose a new hypothesis to explain the persistence of biotic
assemblages and their reorganization or destruction.[419]
First tetrapod tracks from the Upper Permian–Lower Triassic (Lopingian–Induan) eolian strata of the Paraná Basin, southern Brazil, assigned to
the ichnotaxa Dicynodontipus isp. and Chelichnus bucklandi, are described by Francischini et al. (2018).[420]
A study on the biogeographic patterns and severity of extinction of marine taxa during the Permian–Triassic extinction event, evaluating whether
global warming and ocean oxygen loss can mechanistically account for the marine mass extinction, is published by Penn et al. (2018).[421]
A study on changes in the structure of phytoplankton communities in South China during the Permian-Triassic transition is published online by
Lei et al. (2018).[422]
A study on the recovery of benthic invertebrates following the Permian–Triassic extinction event, based on analysis of changes in the species
richness, functional richness, evenness, composition, and ecological complexity of benthic marine communities from the Lower Triassic Servino
Formation (Italy), is published by Foster et al. (2018).[423]
Description of an Early Triassic marine fauna from the Ad Daffah conglomerate in eastern Oman, and on its implications for inferring the ecology
and diversity during the early aftermath of the Permian–Triassic extinction event, is published online by Brosse et al. (2018).[424]
A study on microbial mounds from the Lower Triassic Feixianguan Formation (China), and their implications for inferring the course of biotic
recovery after the Permian–Triassic extinction event, is published by Duan et al. (2018).[425]
A study on the timing and pattern of ecosystem succession during and after the Permian–Triassic extinction event for the duration of the entire
Triassic, as indicated by the changing diversity among non-motile, motile and nektonic animals, is published by Song, Wignall & Dunhill
(2018).[426]
Marine faunas characterized by unusually high levels of both benthic and nektonic taxonomic richness are described from two Early Triassic
sections from South China by Dai et al. (2018).[427]
A study on the historical shifts in geographical ranges and climatic niches of terrestrial vertebrates (both endotherms and ectotherms) based on
data from extant and fossil vertebrates is published by Rolland et al. (2018).[428]
A study on the stratigraphic distribution of the marine vertebrate fossils of the Xingyi Fauna from the Middle Triassic Falang Formation (China) is
published by Lu et al. (2018), who interpret their findings as indicating that the Xingyi Fauna comprises two distinct vertebrate assemblages,
resulting from a major faunal change, which was probably caused by a turnover of their ecological setting from nearshore to offshore.[429]
A study on the patterns of diversity change and extinction selectivity in marine ecosystems during the Triassic–Jurassic interval, especially in
relation to the Triassic–Jurassic extinction event, is published by Dunhill et al. (2018).[430]
A study on the extinction selectivity of marine organisms through the Late Triassic and Early Jurassic, evaluating whether there are any
substantial differences between the hyperthermal events during the Triassic–Jurassic extinction event and Toarcian turnover and the periods of
normal background extinction, is published by Dunhill et al. (2018).[431]
A study on the impact of changes in ocean chemistry beginning in the Mesozoic on the nutritional quality of planktonic algal biomass compared
to earlier phytoplankton is published by Giordano et al. (2018).[432]
A study on the morphological, ecological and behavioural traits linked to the evolution of tail weaponization in extant and fossil amniotes is
published by Arbour & Zanno (2018).[433]
A study on the factors which led to the colonization of marine environments in the evolution of amniotes is published by Vermeij & Motani
(2018).[434]
A review of marine reptile (plesiosaur, ichthyosaur and thalattosuchian) fossils from the Oxfordian sedimentary rocks in Great Britain (United
Kingdom), focusing on the Corallian Group, is published by Foffa, Young & Brusatte (2018), who report evidence of a severe reduction in
observed marine reptile diversity during the Oxfordian.[435]
A study evaluating how the structure of marine reptile ecosystems and their ecologies changed over the roughly 18-million-year history of the
Jurassic Sub-Boreal Seaway of the United Kingdom, as indicated by data from fossil teeth, is published by Foffa et al. (2018).[436]
A diverse footprint assemblage dominated by small mammal tracks is described from the Lower Cretaceous Patuxent Formation (Maryland,
United States) by Stanford et al. (2018), who name a new mammal ichnotaxon Sederipes goddardensis.[437]
A diverse and ecologically informative faunal assemblage is described from the Lower Cretaceous Arundel Clay facies (Maryland, United
States) by Frederickson, Lipka & Cifelli (2018).[438]
Description of an assemblage of Early Cretaceous (Barremian) coprolites from the Las Hoyas Konservat-Lagerstätte (Spain) and a study on
their biological and environmental affinities is published by Barrios-de Pedro et al. (2018).[439]
A study on the taphonomic properties of the inclusions contained in the Las Hoyas coprolites, and their implications for inferring the patterns of
digestive processes of the producers of these coprolites, is published by Barrios-de Pedro & Buscalioni (2018).[440]
Description of isocrinid crinoids belonging to the genus Isocrinus from the Cretaceous amber from Myanmar is published by Mao et al. (2018),
who also report coral columnals and oysters from the amber from Myanmar, and evaluate the age of this amber.[441]
A study on the taxonomic composition of the early Late Cretaceous fauna from the Cliffs of Insanity microvertebrate locality (Mussentuchit
Member, Cedar Mountain Formation; Utah, United States) is published by Avrahami et al. (2018).[442]
Fossil assemblage including plant and vertebrate remains is described from the Turonian Ferron Sandstone Member of the Mancos Shale
Formation (Utah, United States) by Jud et al. (2018), who report turtle and crocodilian remains and an ornithopod sacrum, as well as a large
silicified log assigned to the genus Paraphyllanthoxylon, representing the largest known pre-Campanian flowering plant reported so far and the
earliest documented occurrence of an angiosperm tree more than 1.0 m in diameter.[443]
A study comparing the ecological similarity of Cretaceous cold seep assemblages preserved in the Pierre Shale surrounding the Black Hills and
modern cold-seep assemblages is published online by Laird & Belanger (2018).[444]
A record of foraminifera, calcareous nannoplankton, trace fossils and elemental abundance data from within the Chicxulub crater, dated to
approximately the first 200,000 years of the Paleocene, is presented by Lowery et al. (2018), who report evidence indicating that life reappeared
in the basin just years after the Chicxulub impact and a high-productivity ecosystem was established within 30,000 years.[445]
Vertebrate pathogens found associated with fossil hematophagous arthropods in Dominican, Mexican, Baltic, Canadian and Burmese amber
are reported by Poinar (2018).[446]
Grimaldi et al. (2018) report biological inclusions (fungi, plants, arachnids and insects) in amber from the Paleogene Chickaloon Formation of
Alaska, representing the northernmost deposit of fossiliferous amber from the Cenozoic.[447]
A synthesis of studies on the evolution of the cold‐water coastal North Pacific biota over the last 36 million years, its origins and its influences on
other temperate regions, is presented by Vermeij et al. (2018).[448]
A review of Neogene–Quaternary terrestrial vertebrate sites from the Middle Kura Basin (eastern Georgia and western Azerbaijan) is published
by Bukhsianidze & Koiava (2018).[449]
A study on the reptile and amphibian fossils from the early Pleistocene site of the Russel-Tiglia-Egypte pit near Tegelen (Netherlands) is
published by Villa et al. (2018).[450]
A study on the structure of the animal community known from the Okote Member of the Koobi Fora Formation at East Turkana (Kenya) as
indicated by tracks and skeletal assemblages, and on the interactions of Homo erectus with environment and associated faunas from this site, is
published by Roach et al. (2018).[451]
A revision of Middle Pleistocene faunal record from archeological sites in Africa, and a study on its implications for inferring potential links
between hominin subsistence behavior and the Early Stone Age/Middle Stone Age technological turnover, is published online by Smith et al.
(2018).[452]
Evidence of bird and carnivore exploitation by Neanderthals (cut-marks in golden eagle, raven, wolf and lynx remains) is reported from the Axlor
site (Spain) by Gómez-Olivencia et al. (2018).[453]
A study on the compositions of the faunal and stone artifact assemblages at Liang Bua (Flores, Indonesia), aiming to determine the last
appearance dates of Stegodon, giant marabou stork, Old World vulture belonging to the genus Trigonoceps, and Komodo dragon at the Liang
Bua site, and to determine what raw materials were preferred by hominins from this site ∼50,000–13,000 years ago and whether these are
preferences were similar to those seen in the stone artifact assemblages attributed to Homo floresiensis or to those attributed to modern
humans, is published by Sutikna et al. (2018).[454]
A study on the fossil Sporormiella, pollen and microscopic particles of charcoal recovered from sediments of Lake Mares and Lake Olhos
d’Agua (Brazil) which spanned the time of megafaunal extinction and human arrival in southeastern Brazil, and on their implications for inferring
the timing of the decline of local megafauna and its ecological implications, is published by Raczka, Bush & De Oliveira (2018).[455]
A study evaluating whether the occurrence and decline of spores of Sporormiella in sediments is a good proxy for the occurrence and extinction
of megaherbivores, as indicated by data from Cuddie Springs in south‐eastern Australia, is published by Dodson & Field (2018).[456]
A study evaluating how mega‐herbivore animal species controlled plant community composition and nutrient cycling, relative to other factors
during and after the Late Quaternary extinction event in Great Britain and Ireland, is published by Jeffers et al. (2018).[457]
A study on the impact of the late Quaternary extinction of megafauna on the megafauna-deprived ecosystems is published by Galetti et al.
(2018).[458]
A study on the possible impact of the end of the millennial‐scale climate fluctuations characteristic of the ice age (and the beginning of the more
stable climate regime of the Holocene approximately 11,700 years ago) on the Late Quaternary megafaunal extinctions is published online by
Mann et al. (2018).[459]
A study on the past biodiversity, population dynamics, extinction processes, and the impact of subsistence practices on the vertebrate fauna of
New Zealand, based on analysis of bone fragments from archaeological and paleontological sites covering the last 20,000 years of New
Zealand's past, is published by Seersholm et al. (2018).[460]
A study on changes in plant pathogen communities (fungi and oomycetes) in response to changing climate during late Quaternary, as indicated
by data from solidified deposits of rodent coprolites and nesting material from the central Atacama Desert spanning the last ca. 49,000 years, is
published by Wood et al. (2018).[461]
A study on the parsimony and Bayesian-derived phylogenies of fossil tetrapods, evaluating which of them are in closer agreement with
stratigraphic range data, is published by Sansom et al. (2018).[462]
A study aiming to infer the causes of differences between estimates of speciation and extinction rates based on molecular phylogenies and
those based on fossil record is published by Silvestro et al. (2018), who provide simple mathematical formulae linking the diversification rates
inferred from fossils and phylogenies.[463]
A review of extinction theory and the fossil record of terrestrial diversity crises, comparing past diversity crises of terrestrial vertebrate faunas
with the ongoing Holocene extinction, is published by Padian (2018).[464]
A new metric, which can be used to quantify the term "living fossil" and determine which organisms can be reasonably referred to as such, is
proposed by Bennett, Sutton & Turvey (2018).[465]
A novel non-invasive and label-free tomographic approach to reconstruct the three-dimensional architecture of microfossils based on stimulated
Raman scattering is presented by Golreihan et al. (2018).[466]
Mürer et al. (2018) report on the results of the use of a combination of X-ray diffraction and computed tomography to gain insight into the
microstructure of fossil bones of Eusthenopteron foordi and Discosauriscus austriacus.[467]
A study on melanosomes preserved in the integument and internal organs of extant and fossil frog specimens, evaluating their implications for
inferring colours of extinct animals on the basis of melanosomes preserved in fossil specimens, is published by McNamara et al. (2018).[468]
A study on fossil vertebrate tissues and experimentally matured modern samples, aiming to the mechanism of soft tissue preservation and the
environments that favor it, is published by Wiemann et al. (2018).[469]
A mechanistic model that simulates the history of life on the South American continent, driven by modeled climates of the past 800,000 years, is
presented by Rangel et al. (2018).[470]
A study on temporal trends in biogeography and body size evolution of Australian vertebrates is published by Brennan & Keogh (2018), who
interpret their findings as indicating that gradual Miocene cooling and aridification of Australia correlated with the restricted phenotypic
diversification of multiple ecologically diverse vertebrate groups.[471]
A study evaluating how faithfully stratigraphic ranges of extant Adriatic molluscs are recorded in a series of cores drilled through alluvial, coastal
and shallow-marine strata of the Po Plain (Italy) is published by Nawrot et al. (2018), who also evaluate the implications of their study for
interpretations of the timing, duration and ecological selectivity of mass extinction events in general.[472]
A study on the evolution of morphological disparity (i.e. diversity of anatomical types), as indicated by data from 257 published character
matrices of fossil taxa, is published by Wagner (2018).[473]
A study on the evolution of functional and ecological innovations in temperate marine multicellular organisms inhabiting North Pacific during and
after the Late Eocene is published by Vermeij (2018).[474]
A method for dividing a paleontological dataset into bioregions is proposed by Brocklehurst & Fröbisch (2018), who apply the proposed method
to a study of beta diversity of Paleozoic tetrapods.[475]
A study aiming to estimate the magnitude and potential significance of palaeontological data from specimens housed in museum collections but
not described in published literature is published by Marshall et al. (2018).[476]
Sallan et al. (2018) traced the cradle of evolutionary origins and diversification of fish from the mid-Paleozoic era in nearshore
environments.[477]
Gómez-Olivencia et al. (2018) studied Kebara 2 Neanderthal thorax, aiming to understand how this ancient human species moved and
breathed, based on a 3-D virtual reconstruction.[478]
Smith et al. (2018) examined the teeth of Neanderthal children who lived 250,000 years ago in France, in order to comprehend their nursing
duration, and the effect of lead exposure and severe winters on them.[479]
Wiemann et al. (2018) studied dinosaur's egg colour evolution, in order to unravel whether modern birds inherited egg colour from their non-
avian dinosaur ancestors.[480]

Other research
Other research related to paleontology, including research related to geology, palaeogeography, paleoceanography and paleoclimatology.

A study on the geologic record of Milankovitch climate cycles, extending their analysis into the Proterozoic and aiming to reconstruct the history
of solar system characteristics, is published by Meyers & Malinverno (2018).[481]
A study testing the hypothesis that chemodenitrification, the rapid reduction of nitric oxide by ferrous iron, would have enhanced the flux of
nitrous oxide from Proterozoic seas, leading to nitrous oxide becoming an important constituent of Earth's atmosphere during Proterozoic and
possibly life's primary terminal electron acceptor during the transition from an anoxic to oxic surface Earth, is published by Stanton et al.
(2018).[482]
A study on the effect of different forms of primitive photosynthesis on Earth's early atmospheric chemistry and climate is published by Ozaki et
al. (2018).[483]
A study on the nitrogen isotope ratios, selenium abundances, and selenium isotope ratios from the ∼2.66 billion years old Jeerinah Formation
(Australia), providing evidence of transient surface ocean oxygenation ∼260 million years before the Great Oxygenation Event, is published by
Koehler et al. (2018).[484]
A quantitative estimate of Paleoproterozoic atmospheric oxygen levels is presented by Bellefroid et al. (2018).[485]
A study on the iron mineralogy of the 1.1-billion-year-old Paleolake Nonesuch (Nonesuch Formation), and on its implications for inferring
whether the waters of this lake were oxygenated, is published by Slotznick, Swanson-Hysell & Sperling (2018).[486]
A study on the ocean chemistry at the start of the Mesoproterozoic as indicated by rare earth element, iron-speciation and inorganic carbon
isotope data from the 1,600–1,550 million years old Yanliao Basin, North China Craton is published by Zhang et al. (2018), who report evidence
of a progressive oxygenation event starting at ≈1,570 million years ago, immediately prior to the occurrence of complex multicellular eukaryotes
in shelf areas of the Yanliao Basin.[487]
Evidence of euxinia occurring in the photic zone of the ocean in the Mesoproterozoic, based on measurements of mercury isotope compositions
in late Mesoproterozoic (∼1.1 billion years old) shales from the Atar Group and the El Mreiti Group (Tauodeni Basin, Mauritania), is presented
by Zheng et al. (2018).[488]
A study on the Earth's atmosphere and the productivity of global biosphere 1.4 billion years ago, based on triple oxygen isotope measurements
sedimentary sulfates from the Sibley basin (Ontario, Canada), is published by Crockford et al. (2018).[489]
A study on the isotopically enriched chromium in Mesoproterozoic-aged shales from the Shennongjia Group (China) dating back to 1.35 billion
years ago is published by Canfield et al. (2018), who interpret their findings as document elevated atmospheric oxygen levels through most of
Mesoproterozoic Era, likely sufficient for early crown group animal respiration, but attained over 400 million years before they evolved.[490]
A study on the rate of biotic oxygen production and the attendant large‐scale biogeochemistry of the mid‐Proterozoic Earth system is published
online by Ozaki, Reinhard & Tajika (2018).[491]
A study on the paleomagnetism of the Precambrian Bunger Hills dykes of the Mawson Craton (East Antarctica), and on its tectonic implications,
is published by Liu et al. (2018).[492]
A study on the causes of formation and on global extent of the Great Unconformity is published online by Keller et al. (2018), who interpret their
findings as indicating that this unconformity may record rapid erosion during Neoproterozoic "Snowball Earth" glaciations, and that
environmental and geochemical changes which led to the diversification of multicellular animals may be a direct consequence of Neoproterozoic
glaciation.[493]
A study on the timing of the onset of the Sturtian glaciation, based on new stratigraphic and geochronological data from the upper Tambien
Group (Ethiopia), is published by Scott MacLennan et al. (2018).[494]
A study on abundant pyrite concretions from the topmost Nantuo Formation (China), deposited during the terminal Cryogenian Marinoan
glaciation, is published by Lang et al. (2018), who interpret these concretions as evidence of a transient but widespread presence of marine
euxinia in the aftermath of the Marinoan glaciation.[495]
A study on wave ripples and tidal laminae in the Elatina Formation (Australia), interpreted as evidence of rapid sea level rise in the aftermath of
the Marinoan glaciation, is published by Myrow, Lamb & Ewing (2018).[496]
A study on the environments and food sources that sustained the Ediacaran biota is published by Pehr et al. (2018), who present the lipid
biomarker and nitrogen and carbon isotopic data obtained from late Ediacaran (<560 million years old) strata from seven drill cores and three
outcrops spanning Baltica.[497]
A study on the global ocean redox conditions at a time when the Ediacaran biota began to decline, based on analysis of uranium isotopes in
carbonates from the Dengying Formation (China), is published by Zhang et al. (2018), who interpret their findings as indicative of an episode of
extensive oceanic anoxia at the end of the Ediacaran.[498]
New uranium isotope data from upper Ediacaran to lower Cambrian marine carbonate successions, indicative of short-lived episodes of
widespread marine anoxia near the Ediacaran-Cambrian transition and during Cambrian Stage 2, is presented by Wei et al. (2018), who argue
that the Cambrian explosion might have been triggered by marine redox fluctuations rather than progressive oxygenation.[499]
New δ15N data from late Ediacaran to Cambrian strata from South China is presented by Wang et al. (2018), who interpret their findings as
indicating that ocean redox dynamics were closely coupled with key evolutionary events during the Ediacaran–Cambrian transition.[500]
A study on the isotopic composition and surface temperatures of early Cambrian seas, based on stable oxygen isotope data from the small
shelly fossils from the Comley limestones (United Kingdom), is published by Hearing et al. (2018).[501]
Gougeon et al. (2018) report evidence from the Lower Cambrian Chapel Island Formation (Canada) indicating that a mixed layer of sediment, of
similar structure to that of modern marine sediments (which results from bioturbation by epifaunal and shallow infaunal organisms), was well
established in shallow marine settings by the early Cambrian.[502]
High‐resolution geochemical, sedimentological and biodiversity data from the Cambrian Sirius Passet Lagerstätte (Greenland is presented by
Hammarlund et al. (2018), who aim to assess the chemical conditions in the shelf sea inhabited by the Sirius Passet fauna.[503]
A study on the effects of the rise of bioturbation on global elemental cycles during the Cambrian is published by van de Velde et al. (2018).[504]
A study on the impact of the disruption of sediments caused by Fortunian bioturbation on the ocean chemistry, as indicated by data from the
Chapel Island Formation (Canada), is published by Hantsoo et al. (2018).[505]
A study on the timing of the Sauk transgression in the Grand Canyon region is published by Karlstrom et al. (2018).[506]
A study on the oxygen isotope composition of seawater throughout the Phanerozoic is published by Ryb & Eiler (2018).[507]
A study on changes in the atmospheric concentration of carbon dioxide throughout the Phanerozoic, as indicated by data from a product of
chlorophyll – phytane from marine sediments and oils, is published by Witkowski et al. (2018).[508]
A revised model and a new high-resolution reconstruction of the oxygenation of the Paleozoic atmosphere is presented by Krause et al.
(2018).[509]
A study on the Early Ordovician climate, as indicated by new high-resolution phosphate oxygen isotope record of conodont assemblages from
the Lange Ranch section of central Texas, is published by Quinton et al. (2018), who interpret their findings as consistent with very warm
temperatures during the Early Ordovician.[510]
Jin, Zhan & Wu (2018) present paleontological, sedimentological, and geochemical data to test a hypothesis that a cold surface current became
established by the late Middle Ordovician in the equatorial peri-Gondwana oceans, similar to the eastern equatorial Pacific cold tongue
today.[511]
A review of the history of the definition of the Great Ordovician Biodiversification Event, aiming to clarify its concept and duration, is published by
Servais & Harper (2018).[512]
Evidence from uranium isotopes from Upper Ordovician–lower Silurian marine limestones of Anticosti Island (Canada), indicative of an abrupt
global-ocean anoxic event coincident with the Late Ordovician mass extinction, is presented by Bartlett et al. (2018).[513]
A study on the ocean redox conditions and climate change across a Late Ordovician to Early Silurian on the Yangtze Shelf Sea (China) and
their implications for inferring the causes of the Late Ordovician mass extinction is published by Zou et al. (2018).[514]
A study on the phytoplankton community structure and export production at the end of the Ordovician, as indicated by data from the Vinini
Formation (Nevada, United States), and on their impact on the global carbon cycle and possible relation to the onset of the Late Ordovician
glaciation, is published by Shen et al. (2018).[515]
Evidence of multiple mercury enrichments in the two-step late Frasnian crisis interval from paleogeographically distant successions in Morocco,
Germany and northern Russia is presented by Racki et al. (2018), who interpret their findings as indicating that the Late Devonian extinction
was caused by rapid climatic perturbations promoted in turn by volcanic cataclysm.[516]
A study on the sedimentary facies, oxygen isotopes and the generic conodont composition in two continuous Devonian (late Frasnian to the
end-Famennian) outcrops in the Montagne Noire (Col des Tribes section, France, part of the Armorica microcontinent in the Devonian) and in
the Buschteich section (Germany, part of the Saxo-Thuringian microplate in the Devonian), assessing the water depth, approximate position
relative to the shore and paleotemperatures in the Late Devonian, and evaluating whether environmental changes affected both areas similarly
and at the same pace in the Late Devonian, is published online by Girard et al. (2018).[517]
A study on the climate changes during the period of the Late Devonian extinction (and possibly causing it), inferred from a high-resolution
oxygen isotope record based on conodont apatite from the Frasnian–Famennian transition in South China, is published by Huang, Joachimski &
Gong (2018).[518]
A study on the onset and paleoenvironmental transitions associated with the Hangenberg Crisis within the Cleveland Shale member of the Ohio
Shale is published online by Martinez et al. (2018).[519]
A study on the age of a bentonite layer from Bed 36 in the Frasnian–Famennian succession at the abandoned Steinbruch Schmidt Quarry
(Germany), aiming to determine the precise age of the Frasnian–Famennian boundary and the precise timing of the Late Devonian extinction, is
published by Percival et al. (2018).[520]
A study on the atmospheric oxygen levels through the Phanerozoic, evaluating whether Romer's gap and the concurrent gap in the fossil record
of insects were caused by low oxygen levels, is published by Schachat et al. (2018).[521]
A study on the environmental changes and faunal turnover in the Karoo Basin (South Africa) during the late Permian is published by Viglietti,
Smith & Rubidge (2018).[522]
A study on carbonate microfacies and foraminifer abundances in three Upper Permian sections from isolated carbonate platforms of the
Nanpanjiang Basin (China), indicative of a marine environmental instability up to 60,000 years preceding Permian–Triassic extinction event, is
published online by Tian et al. (2018).[523]
A study on the halogen compositions of Siberian rocks emplaced before and after the eruption of the Siberian flood basalts during the Permian–
Triassic extinction event, and on its implications for inferring the source and nature of volatiles in the Siberian large igneous province, is
published by Broadley et al. (2018).[524]
A study on the impact of sulfur and carbon outgassing from the Siberian Traps flood basalt magmatism on the climate changes at the end of the
Permian is published by Black et al. (2018).[525]
Evidence of enhanced continental chemical weathering at the Permian–Triassic boundary is reported from bulk rock samples from the Meishan
section in South China by Sun et al. (2018), who also evaluate the potential impact of this enhanced weathering on global climate changes
when the end-Permian extinction occurred.[526]
A study on the U-Pb geochronology, biostratigraphy and chemostratigraphy of a highly expanded section at Penglaitan (Guangxi, China) is
published online by Shen et al. (2018), who interpret their findings as indicative of a sudden end-Permian mass extinction that occurred at
251.939 ± 0.031 million years ago.[527]
Evidence of multiple episodes of oceanic anoxia in the Early Triassic, based on U-isotope data from carbonates of the uppermost Permian to
lowermost Middle Triassic Zal section (Iran), is presented by Zhang et al. (2018).[528]
A study on the age of the dinosaur-bearing Triassic Santa Maria Formation and Caturrita Formation (Brazil) is published by Langer, Ramezani &
Da Rosa (2018).[529]
Paleomagnetic and geochronologic study on the Chinle Formation (Petrified Forest National Park, Arizona, United States) is published by Kent
et al. (2018), who report evidence indicating that a 405,000-year orbital eccentricity cycle linked to gravitational interactions with Jupiter and
Venus was already influencing Earth's climate in the Late Triassic.[530]
Evidence of sill intrusions which were likely cause of the Triassic–Jurassic extinction event is reported from the Amazonas and Solimões Basins
(Brazil) by Heimdal et al. (2018).[531]
A study on changes in global bottom water oxygen contents over the Toarcian Oceanic Anoxic Event, based on thallium isotope records from
two ocean basins, is published by Them et al. (2018), who report evidence of global marine deoxygenation of ocean water some 600,000 years
before the classically defined Toarcian Oceanic Anoxic Event.[532]
A study on the atmospheric carbon dioxide concentration levels in the Early Cretaceous based on data from specimens of the fossil conifer
species Pseudofrenelopsis papillosa is published by Jing & Bainian (2018).[533]
A study on the palaeoenvironmental conditions of the seas at high latitudes (60°) of southern South America during the Early Cretaceous is
published online by Gómez Dacal et al. (2018).[534]
A study on the palaeoenvironmental conditions that existed during the time the Upper Cretaceous Winton Formation (Australia) was deposited
is published by Fletcher, Moss & Salisbury (2018).[535]
A study on the age of the Namba Member of the Galula Formation (Tanzania), yielding fossils of Pakasuchus, Rukwasuchus, Rukwatitan and
Shingopana, is published by Widlansky et al. (2018).[536]
A study on the geology, age and palaeoenvironment of the main fossil-bearing beds of the Cretaceous Griman Creek Formation (New South
Wales, Australia) is published online by Bell et al. (2018).[537]
A study on the nature of the fluvial systems of Laramidia during the Late Cretaceous, as indicated by data from vertebrate and invertebrate
fossils from the Kaiparowits Formation of southern Utah, and on the behavior of dinosaurs over these landscapes, is published online by Crystal
et al. (2018).[538]
A study on the rainfall seasonality and freshwater discharge on the Indian subcontinent in the Late Cretaceous (Maastrichtian), based on data
from specimens of the mollusc species Phygraea (Phygraea) vesicularis from the Kallankuruchchi Formation (India), is published by Ghosh et
al. (2018).[539]
Evidence of increased crustal production at mid-ocean ridges at the Cretaceous-Paleogene boundary, indicative of magmatism triggered by
Chicxulub impact, is presented by Byrnes & Karlstrom (2018).[540]
A study on the terrestrial climate in northern China at the Cretaceous-Paleogene boundary, indicating the occurrence of a warming caused by
the onset of Deccan Traps volcanism and the occurrence of extinctions prior to the Chicxulub impact, is published by Zhang et al. (2018).[541]
A study on the oxygen isotopic composition of fish debris from the Global Boundary Stratotype Section and Point for the Cretaceous/Paleogene
boundary at El Kef (Tunisia), indicative of a greenhouse warming in the aftermath of the Chicxulub impact, is published by MacLeod et al.
(2018).[542]
A study on the environmental changes during the global warming following the brief impact winter at the Cretaceous-Paleogene boundary,
based on geochemical, micropaleontological and palynological data from Cretaceous-Paleogene boundary sections in Texas, Denmark and
Spain, is published by Vellekoop et al. (2018).[543]
A study evaluating the utility of oxygen-isotope compositions of fossilised foraminifera tests as proxies for surface- and deep-ocean
paleotemperatures, and its implications for inferring Late Cretaceous and Paleogene deep-ocean and high-latitude surface-ocean temperatures,
published by Bernard et al. (2017)[544] is criticized by Evans et al. (2018).[545][546]
A study on the Paleocene intermediate- and deep-water neodymium-isotope records from the North and South Atlantic Ocean, and on their
implications for inferring the impact of changes in overturning circulation caused by the opening of the Atlantic Ocean on climate changes
culminating in the greenhouse conditions of the Eocene, is published by Batenburg et al. (2018).[547]
Evidence from sulfur-isotope data indicative of a large-scale ocean deoxygenation during the Paleocene–Eocene Thermal Maximum is
presented by Yao, Paytan & Wortmann (2018).[548]
A study on the sources of secondary CO2 inputs after the initial rapid onset of the Paleocene–Eocene Thermal Maximum, contributing to the
prolongation of this event, is published online by Lyons et al. (2018).[549]
Nitrogen isotope data from deposits from the northeast margin of the Tethys Ocean, spanning the Paleocene–Eocene Thermal Maximum, is
presented by Junium, Dickson & Uveges (2018), who interpret their findings as indicating that dramatic change in the nitrogen cycle occurred
during the Paleocene–Eocene Thermal Maximum.[550]
A study on the magnetofossil concentrations preserved within sediments corresponding to the Paleocene–Eocene Thermal Maximum, as well
as on the implications of magnetofossil abundance and morphology signatures for tracing palaeo-environmental conditions during the
Paleocene–Eocene Thermal Maximum, is published by Chang et al. (2018).[551]
A study aiming to evaluate the global extent of surface ocean acidification during the Paleocene–Eocene Thermal Maximum is published by
Babila et al. (2018).[552]
A study on the impact of greenhouse gas forcing and orbital forcing on changes in the seasonal hydrological cycle during the Paleocene–
Eocene Thermal Maximum (for regions where proxy data is available) is published by Kiehl et al. (2018).[553]
Estimates of mean annual terrestrial temperatures in the mid-latitudes during the early Paleogene are presented by Naafs et al. (2018).[554]
A study on the tropical sea-surface temperatures in the Eocene is published by Evans et al. (2018).[555]
A continuous Eocene equatorial sea surface temperature record is presented by Cramwinckel et al. (2018), who also construct a 26-million-year
multi-proxy, multi-site stack of Eocene tropical climate evolution.[556]
A 25-million-year-long alkenone-based record of surface temperature change in the Paleogene from the North Atlantic Ocean is presented by
Liu et al. (2018).[557]
A study on the continental silicate weathering response to the inferred CO2 rise and warming during the Middle Eocene Climatic Optimum is
published by van der Ploeg et al. (2018).[558]
A study on the early stages of development of Asian inland aridity and its underlying mechanisms, based on data from red clay sequence from
the Cenozoic Xorkol Basin (Altyn-Tagh, northeastern Tibetan Plateau), is published by Li et al. (2018), who interpret their findings as indicating
that enhanced Eocene Asian inland aridity was mainly driven by global palaeoclimatic changes rather than being a direct response to the
plateau uplift.[559]
Su et al. (2018) use radiometrically dated plant fossil assemblages to quantify when southeastern Tibet achieved its present elevation, and what
kind of floras existed there at that time.[560]
Description of a plant megafossil assemblage from the Kailas Formation in western part of the southern Lhasa terrane, and a study on its
implications for inferring the elevation history of the southern Tibetan Plateau, is published online by Ai et al. (2018).[561]
New mid-latitude terrestrial climate proxy record for southeastern Australia from the middle Eocene to the middle Miocene, indicative of a
widespread cooling in the Gippsland Basin beginning in the middle Eocene, is presented by Korasidis et al. (2018).[562]
A study on the relationship between the Rovno and Baltic amber deposits, based on stable carbon and hydrogen isotope analyses, is published
by Mänd et al. (2018), who interpret their findings as indicative of distinct origin of Rovno and Baltic amber deposits.[563]
A study on CO2 concentrations during the early Miocene, as indicated by stomatal characteristics of fossil leaves from a late early Miocene
assemblage from Panama and a leaf gas‐exchange model, is published by Londoño et al. (2018).[564]
A study aiming to establish an accurate and precise age model for the eruption of the Columbia River Basalt Group, and to use it to test the
hypothesis that there is a temporal relationship between the eruption of the Columbia River Basalt Group and the mid-Miocene climate
optimum, is published by Kasbohm & Schoene (2018).[565]
A study on the age of the Ashfall Fossil Beds fossil site (Nebraska, United States) is published by Smith et al. (2018).[566]
A study on the causes of changes of environmental conditions in the Paratethys Sea of Central Europe during the middle Miocene is published
online by Simon et al. (2018).[567]
A study on plant fossils spanning 14–4 million years ago from sites in Europe, Asia and East Africa, aiming to test the hypothesis of a single
cohesive biome in the Miocene that extended from Mongolia to East Africa and at its peak covered much of the Old World, is published by Denk
et al. (2018), who interpret data from plant fossil record as disproving the existence of a cohesive savannah biome from eastern Asia to
northeast Africa, formerly inferred from mammal fossil record.[568]
A study on changes in local climate and habitat conditions in central Spain in a period from 9.1 to 6.3 million years ago, and on the diet and
ecology of large mammals from this area in this time period as indicated by tooth wear patterns, is published online by De Miguel, Azanza &
Morales (2018).[569]
Faith (2018) evaluates the aridity index, a widely used technique for reconstructing local paleoclimate and water deficits from oxygen isotope
composition of fossil mammal teeth, arguing that in some taxa altered drinking behavior (influencing oxygen isotope composition of teeth) might
have been caused by dietary change rather than water deficits.[570][571][572]
A study on the likely magnitude of the sea-level drawdown during the Messinian salinity crisis, based on the analysis of the late Neogene faunas
of the Balearic Islands, is published by Mas et al. (2018).[573]
An extensive, buried sedimentary body deposited by the passage of a megaflood from the western to the eastern Mediterranean Sea in the
Pliocene (Zanclean), at the end of the Messinian salinity crisis, is identified in the western Ionian Basin by Micallef et al. (2018).[574]
A study evaluating when the island of Sulawesi (Indonesia) gained its modern shape and size, and determining the timings of diversification of
the three largest endemic mammals on the island (the babirusa, the Celebes warty pig and the anoa) is published by Frantz et al. (2018).[575]
A study on the Pliocene fish fossils from the Kanapoi site (Kenya) and their implications for reconstructing lake and river environments in the
Kanapoi Formation is published online by Stewart & Rufolo (2018).[576]
A study on the hydrological changes in the Limpopo River catchment and in sea surface temperature in the southwestern Indian Ocean for the
past 2.14 million years, and on their implications for inferring the palaeoclimatic changes in southeastern Africa in this time period and their
possible impact on the evolution of early hominins, is published by Caley et al. (2018).[577]
A study on the climate in the areas of the Iberian Peninsula inhabited by hominins during the Early Pleistocene, as indicated by data from
macroflora and pollen assemblages, is published online by Altolaguirre et al. (2018).[578]
Evidence indicating that reduced nutrient upwelling in the Bering Sea and expansion of North Pacific Intermediate Water coincided with the Mid-
Pleistocene Transition cooling is presented by Kender et al. (2018), who assess the potential links between cooling, sea ice expansion, closure
of the Bering Strait, North Pacific Intermediate Water production, reduced high latitude CO2 and nutrient upwelling, and development of the Mid-
Pleistocene Transition.[579]
Domínguez-Rodrigo & Baquedano (2018) evaluate the ability of successful machine learning methods to compare and distinguish various types
of bone surface modifications (trampling marks, crocodile bite marks and cut marks made with stone tools) in archaeofaunal assemblages.[580]
Description of new mammal and fish remains from the Olduvai Gorge site (Tanzania), comparing the mammal assemblage from this site to the
present mammal community of Serengeti, and a study on their implications for reconstructing the paleoecology of this site at ∼1.7–1.4 million
years ago, is published by Bibi et al. (2018).[581]
A study evaluating whether changes of vegetation and diet of East African herbivorous mammals were linked to climatic fluctuations 1.7 million
years ago, based on data from mammal teeth from the Olduvai Gorge site, as well as evaluating whether crocodile teeth from this site may be
used as paleoclimatic indicators, is published by Ascari et al. (2018).[582]
Evidence for progressive aridification in East Africa since about 575,000 years before present, based on data from sediments from Lake Magadi
(Kenya), is presented by Owen et al. (2018), who also evaluate the influence of the increasing Middle- to Late-Pleistocene aridification and
environmental variability on the physical and cultural evolution of Homo sapiens in East Africa.[583]
A study on the environment in the interior of the Arabian Peninsula in the Pleistocene, as indicated by data from stable carbon and oxygen
isotope analysis of fossil mammal tooth enamel from the middle Pleistocene locality of Ti's al Ghadah (Saudi Arabia), is published by Roberts et
al. (2018).[584]
A study on the environmental dynamics before and after the onset of the early Middle Stone Age in the Olorgesailie Basin (Kenya) is published
by Potts et al. (2018).[585]
A study on the chronology of the Acheulean and early Middle Stone Age sedimentary deposits in the Olorgesailie Basin (Kenya) is published by
Deino et al. (2018).[586]
A study on the climatic changes in the Lake Tana area in the last 150,000 years and their implications for early modern human dispersal out of
Africa is published by Lamb et al. (2018).[587]
A study on the proxy evidence for environmental changes during past 116,000 years in lake sediment cores from the Chew Bahir basin, south
Ethiopia (close to the key hominin site of Omo Kibish), and on its implications for inferring the environmental context for dispersal of
anatomically modern humans from northeastern Africa, is published by Viehberg et al. (2018).[588]
A study on the effects of the Toba supereruption in East Africa is published by Yost et al. (2018), who find no evidence of the erupton causing a
volcanic winter in East Africa or a population bottleneck among African populations of anatomically modern humans.[589]
A high-resolution palaeoclimate reconstruction for the Eemian from northern Finland, based on pollen and plant macrofossil record, is presented
by Salonen et al. (2018).[590]
A study on the extent and nature of millennial/centennial-scale climate instability during the Last Interglacial (129–116 thousand years ago), as
indicated by data from joint pollen and ocean proxy analyses in a deep-sea core on the Portuguese Margin (Atlantic Ocean) and speleothem
record from Antro del Corchia cave system (Italy), is published by Tzedakis et al. (2018).[591]
A study on the environmental conditions in the area of present-day Basque Country (Spain) across the Middle to Upper Paleolithic transition,
based on stable isotope data from red deer and horse bones, is published by Jones et al. (2018).[592]
A study on the timing and duration of periods of climate deterioration in the interior of the Iberian Peninsula in the late Pleistocene, evaluating
the impact of climate on the abandonment of inner Iberian territories by Neanderthals 42,000 years ago, is published by Wolf et al. (2018).[593]
A study on the climate changes in Europe during the Middle–Upper Paleolithic transition (based on speleothem records from the Ascunsă Cave
and from the Tăușoare Cave, Romania), and on their implications for the replacement of Neanderthals by modern humans in Europe, is
published by Fernández et al. (2018).[594]
The first reconstructions of terrestrial temperature and hydrologic changes in the south-central margin of the Bering land bridge from the Last
Glacial Maximum to the present are presented by Wooller et al. (2018).[595]
A study on the timing of the latest Pleistocene glaciation in southeastern Alaska and its implication for inferring the route and timing of early
human migration to the Americas is published by Lesnek et al. (2018).[596]
Quantitative estimates of climate in western North America over the past 50,000 years, based on data from plant community composition of
more than 600 individual paleomiddens, are presented by Harbert & Nixon (2018).[597]
A study on the impact of major, abrupt environmental changes over the past 30,000 years on the Great Barrier Reef is published by Webster et
al. (2018).[598]
Evidence of sea level drop relative to the modern level at the shelf edge of the Great Barrier Reef between 21,900 and 20,500 years ago,
followed by period of sea level rise lasting around 4,000 years, is presented by Yokoyama et al. (2018).[599]
A study on the fossil-bound nitrogen isotope records from the Southern Ocean is published by Studer et al. (2018), who interpret their findings
as indicative of an acceleration of nitrate supply to the Southern Ocean surface from underlying deep water during the Holocene, possibly
contributing to the Holocene atmospheric CO2 rise.[600]
A study on the causes of replacement of mature rainforests by a forest–savannah mosaic in Western Central Africa between 3,000 y ago and
2,000 years ago, based on a continuous record of 10,500 years of vegetation and hydrological changes from Lake Barombi Mbo (Cameroon)
inferred from changes in carbon and hydrogen isotope compositions of plant waxes, is published by Garcin et al. (2018), who interpret their
findings as indicating that humans triggered the rainforest fragmentation 2,600 years ago.[601][602][603][604][605]
A study on the vegetational and climatic changes since the last glacial period, based on data from 594 sites worldwide, and aiming to estimate
the extent of future ecosystem changes under alternative scenarios of global warming, is published by Nolan et al. (2018).[606]
A study on the changing ecology of woodland vegetation of southern mainland Greece during the late Pleistocene and the early-mid Holocene,
and on the ecological context of the first introduction of crop domesticates in the southern Greek mainland, as indicated by data from carbonized
fuel wood waste from the Franchthi Cave, is published by Asouti, Ntinou & Kabukcu (2018).[607]
A large impact crater found beneath Hiawatha Glacier (Greenland), most likely formed during the Pleistocene, is reported by Kjær et al.
(2018).[608]
A study assessing the similarity of future projected climate states to the climate during the Early Eocene, the Mid-Pliocene, the Last Interglacial
(129–116 ka), the Mid-Holocene (6 ka), preindustrial (ca. 1850 CE), and the 20th century is published by Burke et al. (2018).[609]

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