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{{Short description|Extinct clade of dinosaurs}}
{{Automatic taxobox
| name = Enantiornithes
| fossil_range = <br/>[[Early Cretaceous]]<ref name=eopengornis>{{Cite journal | doi = 10.1111/bij.12313| title = Insights into the evolution of rachis dominated tail feathers from a new basal enantiornithine (Aves: Ornithothoraces)| journal = Biological Journal of the Linnean Society| volume = 113| issue = 3| pages = 805–819| year = 2014| last1 = Wang | first1 = X. | last2 = O'Connor | first2 = J. K. | last3 = Zheng | first3 = X. | last4 = Wang | first4 = M. | last5 = Hu | first5 = H. | last6 = Zhou | first6 = Z. | doi-access = free }}</ref>&ndash;[[Late Cretaceous]], {{Fossil range|136|66|earliest=154}}
| image = Zhouornis hani.png
| image_caption = Fossil specimen of a [[Bohaiornithidae|bohaiornithid]] (''[[Zhouornis hani]]'')
| taxon = Enantiornithes
| authority = [[Cyril Walker (palaeontologist)|Walker]], 1981
| subdivision_ranks = Subgroups
| subdivision = *[[Avisauridae]]
*[[Bohaiornithidae]]<ref name=bohaiornithidae/>
*[[Gobipterygidae]]
*[[Longipterygidae]]
*[[Pengornithidae]]<ref name=eopengornis/>
and see text
}}

The '''Enantiornithes''', also known as enantiornithines or enantiornitheans in literature, are a group of extinct [[Avialae|avialans]] ("birds" in the broad sense), the most abundant and diverse group known from the [[Mesozoic era]].<ref name="chiappe&walker2002">{{cite book |first1=Luis M. |last1=Chiappe |first2=Cyril A. |last2=Walker |chapter=Skeletal Morphology and Systematics of the Cretaceous Euenantiornithes (Ornithothoraces: Enantiornithes) |chapter-url=https://books.google.com/books?id=2MQeh1KCp7sC&pg=PA240 |pages=240–67 |editor1-first=Luis M. |editor1-last=Chiappe |editor2-first=Lawrence M. |editor2-last=Witmer |year=2002 |title=Mesozoic Birds: Above the Heads of Dinosaurs |publisher=University of California Press |isbn=978-0-520-20094-4}}</ref><ref>{{cite book |last1=Chiappe |first1=Luis M. |year=2007 |title=Glorified Dinosaurs: The Origin and Early Evolution of Birds |publisher=John Wiley and Sons |location=Hoboken, New Jersey |isbn=978-0-471-24723-4}}{{page needed|date=April 2014}}</ref><ref>{{cite journal |last1=O'Connor |first1=Jingmai K. |last2=Chiappe |first2=Luis M. |last3=Gao |first3=Chunling |last4=Zhao |first4=Bo |title=Anatomy of the Early Cretaceous Enantiornithine Bird Rapaxavis pani |journal=Acta Palaeontologica Polonica |date=September 2011 |volume=56 |issue=3 |pages=463–475 |doi=10.4202/app.2010.0047 |s2cid=55311115 |doi-access=free }}</ref> Almost all retained teeth and clawed fingers on each wing, but otherwise looked much like modern birds externally. Over seventy species of Enantiornithes have been named, but some names represent only single bones, so it is likely that not all are valid. The Enantiornithes became extinct at the [[Cretaceous–Paleogene boundary]], along with [[Hesperornithes]] and all other non-avian [[dinosaur]]s.

== Discovery and naming ==
The first Enantiornithes to be discovered were incorrectly referred to modern bird groups. For example, the first known species of Enantiornithes, ''[[Gobipteryx minuta]]'', was originally considered a [[paleognath]] related to [[ostrich]]es and [[tinamou]].<ref>{{cite journal |last1=Elzanowski |first1=Andrzej |author-link=Andrzej Elżanowski |year=1974 |url=http://www.palaeontologia.pan.pl/Archive/1974_30_103-109_32-33.pdf |title=Preliminary note on the palaeognathous bird from the Upper Cretaceous of Mongolia |journal=Palaeontologia Polonica |volume=29 |pages=103–9 |s2cid=53487062 }}</ref> The Enantiornithes were first recognized as a distinct lineage, or "subclass" of birds, by [[Cyril A. Walker]] in 1981. Walker made this discovery based on some partial remains from the late [[Cretaceous]] [[Period (geology)|period]] of what is now [[Argentina]], which he assigned to a new genus, ''[[Enantiornis]]'', giving the entire group its name. Since the 1990s, many more complete specimens of Enantiornithes have been discovered, and it was determined that a few previously described "birds" (e.g. ''[[Iberomesornis]]'', ''[[Cathayornis]]'', and ''[[Sinornis]]'') were also Enantiornithes.

The name "Enantiornithes" means "opposite birds", from [[Ancient Greek]] ''enantios'' ({{lang|grc|ἐνάντιος}}) "opposite" + ''ornithes'' ({{lang|grc|ὄρνιθες}}) "birds" . The name was coined by [[Cyril Alexander Walker]] in his landmark paper which established the group.<ref name="walker1981">{{cite journal |last1=Walker |first1=C.A. |year=1981 |doi=10.1038/292051a0 |title=New subclass of birds from the Cretaceous of South America |journal=Nature |volume=292 |issue=5818 |pages=51–3|bibcode=1981Natur.292...51W |s2cid=4340858 }}</ref> In his paper, Walker explained what he meant by "opposite":

{{blockquote|Perhaps the most fundamental and characteristic difference between the Enantiornithes and all other birds is in the nature of the articulation between the [[scapula]] [...] and the [[coracoid]], where the 'normal' condition is completely reversed.<ref name="walker1981"/>}}

This refers to an anatomical feature – the articulation of the [[shoulder]] bones – which has a concave-convex socket joint between the ''scapula'' (shoulder blade) and ''coracoid'' (the primary bone of the shoulder girdle in vertebrates other than mammals) that is the reverse of that of modern birds. Specifically, in the Enantiornithes, the scapula is [[wiktionary:Concave|concave]] and dish-shaped at this joint, and the coracoid is convex.<ref name="chiappe&walker2002"/>{{rp|249–50}} In modern birds, the coracoscapular joint has a concave coracoid and convex scapula.<ref>{{cite book |first1=Sylvia |last1=Hope |chapter=The Mesozoic Radiation of Neornithes |pages=339–88 |editor1-first=Luis M. |editor1-last=Chiappe |editor2-first=Lawrence M. |editor2-last=Witmer |year=2002 |title=Mesozoic Birds: Above the Heads of Dinosaurs |publisher=University of California Press |isbn=978-0-520-20094-4}}</ref><ref>{{cite journal |last1=Mayr |first1=G. |year=2021 |doi=10.1007/s00435-021-00528-2 |title=The coracoscapular joint of neornithine birds—extensive homoplasy in a widely neglected articular surface of the avian pectoral girdle and its possible functional correlates |journal= Zoomorphology |volume=140 |issue=2 |pages=217–28 |s2cid=236397491 |doi-access=free }}</ref>

Walker was not clear on his reasons for giving this name in the etymology section of his paper, and this ambiguity led to some confusion among later researchers. For example, [[Alan Feduccia]] stated in 1996:
{{blockquote|The birds are so named because, among many distinctive features, there is a unique formation of the triosseal canal and the metatarsals are fused proximally to distally, the opposite of that in modern birds<ref>{{cite book |last1=Feduccia |first1=Alan |year=1996 |title=The Origin and Evolution of Birds |url=https://archive.org/details/originevolutiono0000fedu |url-access=registration |publisher=Yale University Press |location=New Haven |isbn=978-0-300-06460-5}}{{page needed|date=April 2014}}</ref>}}

Feduccia's point about the ''[[tarsometatarsus]]'' (the combined upper foot and ankle bone) is correct, but Walker did not use this reasoning in his original paper. Walker never described the fusion of the tarsometatarsus as opposite, but rather as "Only partial". Also, it is not certain that Enantiornithes had triosseal canals, since no fossil preserves this feature.<ref name="chiappe&walker2002"/>

As a group, the Enantiornithes are often referred to as "enantiornithines" in literature. However, several scientists have noted that this is incorrect, because following the standard rules for forming the names of animal groups, it implies reference only to the subfamily [[Enantiornithinae]]. Following the naming conventions used for modern birds as well as extinct groups, it has been pointed out that the correct term is "enantiornithean".<ref name="harrisetal2006">{{cite journal |last1=Harris |first1=Jerald D. |last2=Lamanna |first2=Matthew C. |last3=You |first3=Hai-lu |last4=Ji |first4=Shu-an |last5=Ji |first5=Qiang  |title=A second enantiornithean (Aves: Ornithothoraces) wing from the Early Cretaceous Xiagou Formation near Changma, Gansu Province, People's Republic of China |journal=Canadian Journal of Earth Sciences |date=18 May 2006 |volume=43 |issue=5 |pages=547–554 |doi=10.1139/e06-007 |bibcode=2006CaJES..43..547H }}</ref><ref name="youetal2006">{{cite journal |last1=You |first1=Hai-lu |last2=Lamanna |first2=Matthew C. |last3=Harris |first3=Jerald D. |last4=Chiappe |first4=Luis M. |last5=O'Connor |first5=Jingmai |last6=Ji |first6=Shu-an |last7=Lü |first7=Jun-chang |last8=Yuan |first8=Chong-xi |last9=Li |first9=Da-qing |last10=Zhang |first10=Xing |last11=Lacovara |first11=Kenneth J. |last12=Dodson |first12=Peter |last13=Ji |first13=Qiang |title=A Nearly Modern Amphibious Bird from the Early Cretaceous of Northwestern China |journal=Science |date=16 June 2006 |volume=312 |issue=5780 |pages=1640–1643 |doi=10.1126/science.1126377 |pmid=16778053 |bibcode=2006Sci...312.1640Y |s2cid=42723583 }}</ref>

==Origin and range==
''[[Praeornis]]'', from the [[Oxfordian (stage)|Oxfordian]]-[[Kimmeridgian]] of [[Kazakhstan]], may have been the earliest known member of Enantiornithes according to Agnolin et al. (2017).<ref name="praeornis20172">Agnolin, F.L., Rozadilla, S., and Ismar de Souza Carvalho (2017). ''Praeornis sharovi'' Rautian, 1978 a fossil feather from the early Late Jurassic of Kazakhstan. ''Historical Biology''. {{doi|10.1080/08912963.2017.1413102}}</ref>

Birds with confidently identified characteristics of Enantiornithes found in [[Albian]] of [[Australia]], [[Maastrichtian]] of South America, and [[Campanian]] of [[Mexico]] (''[[Alexornis]]''<ref>{{cite book|author=Pierce Brodkorb|url=http://www.sil.si.edu/smithsoniancontributions/Paleobiology/pdf_hi/SCtP-0027.pdf|title=Discovery of a Cretaceous bird, apparently ancestral to the orders Coraciiformes and Piciformes (Aves: Carinatae) '''[File size 70 MB]'''|date=1976|publisher=Smithsonian Contributions to Paleobiology|volume=27|pages=67–73|archive-url=https://web.archive.org/web/20141019235100/https://www.sil.si.edu/smithsoniancontributions/Paleobiology/pdf_hi/SCtP-0027.pdf|archive-date=19 October 2014|url-status=dead}}</ref>), [[Mongolia]] and western edge of prehistoric Asia suggest a worldwide distribution of this group or in the relatively warm regions, at least.<ref>{{cite book|author=L. A. Nesov, A. A. Yarkov|date=1989|url=http://museionsajtyarkova.ru/downloads/publication/Novye%20pticy%20mela-paleogena.pdf|title=Новые птицы мел-палеогена СССР и некоторые замечания по истории возникновения и эволюции класса (New Cretaceous-Paleogene birds of USSR and some remarks about history of the origin and evolution of class)|publisher=USSR Academy of scienses|volume=197|page=82|lang=ru|archive-url=https://web.archive.org/web/20190327231749/http://museionsajtyarkova.ru/downloads/publication/Novye%20pticy%20mela-paleogena.pdf|archive-date=27 March 2019|url-status=live}}</ref> Enantiornithes have been found on every continent except [[Antarctica]]. Fossils attributable to this group are exclusively [[Cretaceous]] in age, and it is believed that the Enantiornithes became extinct at the same time as their non-avialan [[dinosaur]] relatives. The earliest known Enantiornithes are from the [[Early Cretaceous]] of [[Spain]] (e.g. ''[[Noguerornis]]'') and [[China]] (e.g. ''[[Protopteryx]]'') and the latest from the [[Late Cretaceous]] of North and South America (e.g. ''[[Avisaurus]]'' and ''[[Enantiornis]]''). The widespread occurrence of this group suggests that at least some Enantiornithes were able to cross oceans under their own power; they are the first known avialan lineage with a global distribution.

==Description==
[[File:Iberomesornis romerali by durbed.jpg|left|thumb|A life restoration of ''[[Iberomesornis]],'' a species of early Enantiornithes]]
Many fossils of Enantiornithes are very fragmentary, and some species are only known from a piece of a single bone. Almost all specimens that are complete, in full articulation, and with soft tissue preservation are known from [[Las Hoyas]] in [[Province of Cuenca|Cuenca]], [[Spain]] and the [[Jehol group]] in [[Liaoning]] ([[People's Republic of China|China]]). Extraordinary remains of Enantiornithes have also been preserved in [[Burmese amber]] deposits dated to 99 million years ago and include hatchlings described in 2017<ref name="ambercorpse">{{cite journal|last1=Xing|first1=Lida|last2=O'Connor|first2=Jingmai K.|last3=McKellar|first3=Ryan C.|last4=Chiappe|first4=Luis M.|last5=Tseng|first5=Kuowei|last6=Li|first6=Gang|last7=Bai|first7=Ming|date=September 2017|title=A mid-Cretaceous enantiornithine (Aves) hatchling preserved in Burmese amber with unusual plumage|journal=Gondwana Research|volume=49|pages=264–277|bibcode=2017GondR..49..264X|doi=10.1016/j.gr.2017.06.001}}</ref> and 2018,<ref name=":0">{{cite journal|last1=Xing|first1=Lida|last2=O'Connor|first2=Jingmai K.|last3=McKellar|first3=Ryan C.|last4=Chiappe|first4=Luis M.|last5=Bai|first5=Ming|last6=Tseng|first6=Kuowei|last7=Zhang|first7=Jie|last8=Yang|first8=Haidong|last9=Fang|first9=Jun|last10=Li|first10=Gang|date=February 2018|title=A flattened enantiornithine in mid-Cretaceous Burmese amber: morphology and preservation|journal=Science Bulletin|volume=63|issue=4|pages=235–243|bibcode=2018SciBu..63..235X|doi=10.1016/j.scib.2018.01.019|pmid=36659012 |doi-access=free}}</ref> as well as isolated body parts such as wings<ref name="amber_enant" /><ref name=":2">{{cite journal|last1=Xing|first1=Lida|last2=McKellar|first2=Ryan C.|last3=O'Connor|first3=Jingmai K.|last4=Bai|first4=Ming|last5=Tseng|first5=Kuowei|last6=Chiappe|first6=Luis M.|date=30 January 2019|title=A fully feathered enantiornithine foot and wing fragment preserved in mid-Cretaceous Burmese amber|journal=Scientific Reports|volume=9|issue=1|pages=927|bibcode=2019NatSR...9..927X|doi=10.1038/s41598-018-37427-4|pmc=6353931|pmid=30700773}}</ref><ref>{{cite journal|last1=Xing|first1=Lida|last2=McKellar|first2=Ryan C.|last3=O'Connor|first3=Jingmai K.|date=June 2020|title=An unusually large bird wing in mid-Cretaceous Burmese amber|journal=Cretaceous Research|volume=110|pages=104412|doi=10.1016/j.cretres.2020.104412|bibcode=2020CrRes.11004412X |s2cid=213510021}}</ref> and feet.<ref name=":2" /><ref>{{Cite journal|last1=Xing|first1=Lida|last2=O'Connor|first2=Jingmai K.|last3=Chiappe|first3=Luis M.|last4=McKellar|first4=Ryan C.|last5=Carroll|first5=Nathan|last6=Hu|first6=Han|last7=Bai|first7=Ming|last8=Lei|first8=Fumin|date=2019-07-22|title=A New Enantiornithine Bird with Unusual Pedal Proportions Found in Amber|journal=Current Biology|language=English|volume=29|issue=14|pages=2396–2401.e2|doi=10.1016/j.cub.2019.05.077|issn=0960-9822|pmid=31303484|s2cid=195887085|doi-access=free}}</ref> These amber remains are among the most well-preserved of any mesozoic dinosaur. Fossils of this clade have been found in both inland and marine sediments, suggesting that they were an ecologically diverse group.

Enantiornithes appear to have included waders, swimmers, granivores, insectivores, fishers, and raptors. The vast majority of Enantiornithes were small, between the size of a [[Old World sparrow|sparrow]] and a [[starling]],<ref name="zhang(2013)">{{cite journal|last1=Zhang|first1=Zihui|last2=Chiappe|first2=Luis M.|last3=Han|first3=Gang|last4=Chinsamy|first4=Anusuya|year=2013|title=A large bird from the Early Cretaceous of China: new information on the skull of enantiornithines|journal=Journal of Vertebrate Paleontology|volume=33|issue=5|pages=1176–89|doi=10.1080/02724634.2013.762708|bibcode=2013JVPal..33.1176Z |s2cid=84677039}}</ref> however display considerable variation in size with some species. The largest species in this clade include ''[[Pengornis houi]]'',<ref name="AnatomyMay2008">{{cite journal|last1=Zhou|first1=Zhonghe|last2=Clarke|first2=Julia|last3=Zhang|first3=Fucheng|date=May 2008|title=Insight into diversity, body size and morphological evolution from the largest Early Cretaceous enantiornithine bird|journal=Journal of Anatomy|volume=212|issue=5|pages=565–77|doi=10.1111/j.1469-7580.2008.00880.x|pmc=2409080|pmid=18397240}}</ref> ''[[Xiangornis shenmi]]'',<ref>{{cite journal|last1=Hu|first1=Dongyu|last2=Xu|first2=Xing|last3=Hou|first3=Lianhai|last4=Sullivan|first4=Corwin|year=2012|title=A New Enantiornithine Bird from the Lower Cretaceous of Western Liaoning, China, and Its Implications for Early Avian Evolution|journal=Journal of Vertebrate Paleontology|volume=32|issue=3|pages=639–45|doi=10.1080/02724634.2012.652321|bibcode=2012JVPal..32..639H |s2cid=85942925}}</ref> ''[[Zhouornis hani]]'',<ref name="zhang(2013)" /> and [[Mirarce|''Mirarce eatoni'']],''<ref>{{cite journal|last1=Atterholt|first1=Jessie|last2=Hutchison|first2=J. Howard|last3=O'Connor|first3=Jingmai K.|date=13 November 2018|title=The most complete enantiornithine from North America and a phylogenetic analysis of the Avisauridae|journal=PeerJ|volume=6|pages=e5910|doi=10.7717/peerj.5910|pmc=6238772|pmid=30479894 |doi-access=free }}</ref>'' (with the latter species being described as similar in size to modern turkeys,) although at least a few larger species may have also existed, including a potentially crane-sized species known only from footprints in the [[Eumeralla Formation]] (and possibly also represented in the [[Wonthaggi Formation]] by a single [[furcula]]).<ref>{{cite journal|last1=Martin|first1=Anthony J.|last2=Vickers-Rich|first2=Patricia|last3=Rich|first3=Thomas H.|last4=Hall|first4=Michael|last5=Angielczyk|first5=Kenneth|date=January 2014|title=Oldest known avian footprints from Australia: Eumeralla Formation (Albian), Dinosaur Cove, Victoria|journal=Palaeontology|volume=57|issue=1|pages=7–19|doi=10.1111/pala.12082|bibcode=2014Palgy..57....7M |doi-access=free}}</ref> Among the smallest described specimens are unnamed hatchlings, although the holotype specimens of [[Parvavis|''Parvavis chuxiongensis'']]<ref>{{Cite journal|last1=Wang|first1=Min|last2=Zhou|first2=Zhonghe|last3=Xu|first3=Guanghui|date=2014-01-01|title=The first enantiornithine bird from the Upper Cretaceous of China|journal=Journal of Vertebrate Paleontology|volume=34|issue=1|pages=135–145|doi=10.1080/02724634.2013.794814|bibcode=2014JVPal..34..135W |s2cid=85255564|issn=0272-4634}}</ref> and [[Cratoavis|''Cratoavis cearensis'']]<ref name=Carvalhoetal2015>{{Cite journal|last1=Carvalho|first1=Ismar|last2=Novas|first2=Fernando|last3=Agnolin|first3=Federico|last4=Isasi|first4=Marcelo|last5=Freitas|first5=Francisco|last6=Andrade|first6=José|date=2015-06-05|title=A new genus and species of enantiornithine bird from the Early Cretaceous of Brazil|url=https://www.researchgate.net/publication/279516967|journal=Brazilian Journal of Geology|volume=45|issue=2|pages=161–171|doi=10.1590/23174889201500020001|doi-access=free}}</ref> are comparable in size to small tits or hummingbirds.

===Skull===
[[File:Bohaiornis skull reconstruction.png|thumb|A reconstruction of the skull of ''[[Bohaiornis]],'' a [[Bohaiornithidae|bohaiornithid]].]]
Given their wide range of habitats and diets, the cranial morphology of Enantiornithes varied considerably between species. Skulls of Enantiornithes combined a unique suite of primitive and advanced features. As in more primitive avialans like ''[[Archaeopteryx]]'', they retained several separate cranial bones, small [[premaxilla]]e (bones of the snout tip) and most species had toothy jaws rather than toothless beaks. Only a few species, such as ''[[Gobipteryx minuta]]'', were fully toothless and had beaks. They also had simple [[quadrate bone]]s, a complete bar separating each [[Orbit (anatomy)|orbit]] (eye hole) from each [[antorbital fenestra]], and dentaries (the main toothed bones of the lower jaw) without forked rear tips. A [[squamosal bone]] is preserved in an indeterminate juvenile specimen, while a [[Postorbital bone|postorbital]] is preserved in ''[[Shenqiornis]]'' and ''[[Pengornis]]''. In modern birds these bones are assimilated into the cranium. Some Enantiornithes may have had their [[temporal fenestrae]] (holes in the side of the head) merged into the orbits as in modern birds due to the postorbitals either not being present or not being long enough to divide the openings.<ref name="oconnoretal2011skulls">{{cite journal |last1=O'Connor |first1=Jingmai K. |last2=Chiappe |first2=Luis M. |title=A revision of enantiornithine (Aves: Ornithothoraces) skull morphology |journal=Journal of Systematic Palaeontology |date=28 February 2011 |volume=9 |issue=1 |pages=135–157 |doi=10.1080/14772019.2010.526639 |bibcode=2011JSPal...9..135O |s2cid=86503357 }}</ref> A [[quadratojugal bone]], which in modern birds is fused to the jugal, is preserved in ''[[Pterygornis]]''.<ref name="Pterygornis" /> The presence of these primitive features of the skull would have rendered the Enantiornithes capable of only limited [[cranial kinesis]] (the ability to move the jaw independent of the cranium).<ref>{{cite journal |last1=Wang |first1=Min |last2=Hu |first2=Han |title=A Comparative Morphological Study of the Jugal and Quadratojugal in Early Birds and Their Dinosaurian Relatives |journal=The Anatomical Record |date=January 2017 |volume=300 |issue=1 |pages=62–75 |doi=10.1002/ar.23446 |pmid=28000410 |s2cid=3649504 |doi-access=free }}</ref>

===Wing===
[[File:Mummified precocial bird wings in mid-Cretaceous Burmese amber (2016) fig. 1.png|thumb|A [[X-ray microtomography|micro-CT]] scan of an amber-encased wing attributable to Enantiornithes showing rachises, skin, muscle and claws.|left]]
As a very large group of birds, the Enantiornithes displayed a high diversity of different body plans based on differences in ecology and feeding, reflected in an equal diversity of wing forms, many paralleling adaptations to different lifestyles seen in modern birds. In general, the wings of Enantiornithes were advanced compared to more primitive avialans like ''Archaeopteryx'', and displayed some features related to flight similar to those found in the lineage leading to modern birds, the [[Ornithuromorpha]]. While most Enantiornithes had claws on at least some of their fingers, many species had shortened hands, a highly mobile shoulder joint, and proportional changes in the wing bones similar to modern birds. Like modern birds, Enantiornithes had [[alula]]s, or "bastard wings", small forward-pointing arrangements of feathers on the first digit that granted higher maneuverability in the air and aided in precise landings.<ref name=chiappe2009>{{cite journal |first1=Luis M. |last1=Chiappe |year=2009 |title=Downsized Dinosaurs: The Evolutionary Transition to Modern Birds |journal=Evolution: Education and Outreach |volume=2 |issue=2 |pages=248–56 |doi=10.1007/s12052-009-0133-4|doi-access=free }}</ref>

Several wings with preserved feathers have been found in [[Burmese amber]]. These are the first complete [[Mesozoic]] [[dinosaur]] remains preserved this way (a few isolated feathers are otherwise known, unassigned to any species), and one of the most exquisitely preserved dinosaurian fossils known.<ref name=enant_amber_nature>{{cite journal |last1=Becker |first1=Rachel |title=Bird wings trapped in amber are a fossil first from the age of dinosaurs |journal=Nature |date=28 June 2016 |doi=10.1038/nature.2016.20162 |s2cid=88601510 }}</ref> The preserved wings show variations in feather pigment and prove that Enantiornithes had fully modern feathers, including barbs, barbules, and hooklets, and a modern arrangement of wing feather including long flight feathers, short coverts, a large alula and an undercoat of down.<ref name=amber_enant>{{cite journal |last1=Xing |first1=Lida |last2=McKellar |first2=Ryan C. |last3=Wang |first3=Min |last4=Bai |first4=Ming |last5=O'Connor |first5=Jingmai K. |last6=Benton |first6=Michael J. |last7=Zhang |first7=Jianping |last8=Wang |first8=Yan |last9=Tseng |first9=Kuowei |last10=Lockley |first10=Martin G. |last11=Li |first11=Gang |last12=Zhang |first12=Weiwei |last13=Xu |first13=Xing |title=Mummified precocial bird wings in mid-Cretaceous Burmese amber |journal=Nature Communications |date=28 June 2016 |volume=7 |issue=1 |pages=12089 |doi=10.1038/ncomms12089 |pmid=27352215 |pmc=4931330 |bibcode=2016NatCo...712089X }}</ref>

One fossil of Enantiornithes shows wing-like feather tufts on its legs, similar to ''Archaeopteryx''. The leg feathers are also reminiscent of the four-winged dinosaur ''[[Microraptor]]'', however differ by the feathers being shorter, more disorganized (they do not clearly form a wing) and only extend down to the ankle rather than along the foot.<ref name=legfeather>{{cite journal |first1=Fucheng |last1=Zhang |first2=Zhonghe |last2=Zhou |date=October 2004 |title=Palaeontology: Leg feathers in an Early Cretaceous bird |journal=Nature |volume=431 |issue=7011 |pages=925 |pmid=15496911 |doi=10.1038/431925a |bibcode=2004Natur.431..925Z |s2cid=4322054 |doi-access=free }}</ref>

===Tail===
[[image:Rapaxavis.jpg|thumb|Fossil skeleton of ''[[Rapaxavis pani]]'' (a [[Longipterygidae|longipterygid]]) with a preserved [[pygostyle]]]]
Clarke ''et al.'' (2006) surveyed all fossils of Enantiornithes then known and concluded that none had preserved tail feathers that formed a lift-generating fan, as in modern birds. They found that all avialans outside of [[Euornithes]] (the clade they referred to as [[Ornithurae]]) with preserved tail feathers had only short coverts or elongated paired tail plumes. They suggested that the development of the [[pygostyle]] in Enantiornithes must have been a function of tail shortening, not the development of a modern tail feather anatomy. These scientists suggested that a fan of tail feathers and the associated musculature needed to control them, known as the ''rectrical bulb'', evolved alongside a short, triangular pygostyle, like the ones in modern birds, rather than the long, rod- or dagger-shaped pygostyles in more primitive avialans like the Enantiornithes. Instead of a feather fan, most Enantiornithes had a pair of long specialized pinfeathers similar to those of the extinct ''[[Confuciusornis]]'' and certain extant [[Bird-of-paradise|birds-of-paradise]].<ref name="Clarkeetal2006">{{cite journal |first1=Julia A. |last1=Clarke |first2=Zhonghe |last2=Zhou |first3=Fucheng |last3=Zhang |date=March 2006 |title=Insight into the evolution of avian flight from a new clade of Early Cretaceous ornithurines from China and the morphology of ''Yixianornis grabaui'' |journal=Journal of Anatomy |volume=208 |issue=3 |pages=287–308 |pmid=16533313 |pmc=2100246 |doi=10.1111/j.1469-7580.2006.00534.x }}</ref>

However, further discoveries showed that at least among basal Enantiornithes, tail anatomy was more complex than previously thought. One genus, ''[[Shanweiniao]]'', was initially interpreted as having at least four long tail feathers that overlapped each other<ref name="O'connoretal.2009">{{cite journal |last1=O'Connor |first1=Jingmai K. |last2=Wang |first2=Xuri |last3=Chiappe |first3=Luis M. |last4=Gao |first4=Chunling |last5=Meng |first5=Qingjin |last6=Cheng |first6=Xiaodong |last7=Liu |first7=Jinyuan |title=Phylogenetic support for a specialized clade of Cretaceous enantiornithine birds with information from a new species |journal=Journal of Vertebrate Paleontology |date=12 March 2009 |volume=29 |issue=1 |pages=188–204 |doi=10.1080/02724634.2009.10010371 |bibcode=2009JVPal..29..188O |s2cid=196607241 }}</ref> and might have formed a lift-generating surface similar to the tail fans of [[Euornithes|Euronithes]],<ref name=hongshan2014/> though a later study indicates that ''Shanweiniao'' was more likely to have [[rachis]]-dominated tail feathers similar to feathers present in ''[[Paraprotopteryx]]''.<ref name="chiappeavis" /> ''[[Chiappeavis]]'', a primitive [[Pengornithidae|pengornithid]], had a fan of tail feathers similar to that of more primitive avialans like ''[[Sapeornis]]'', suggesting that this might have been the ancestral condition, with pinfeathers being a feature evolved several times in early avialans for display purposes.<ref name="chiappeavis">{{cite journal |last1=O'Connor |first1=Jingmai K. |last2=Wang |first2=Xiaoli |last3=Zheng |first3=Xiaoting |last4=Hu |first4=Han |last5=Zhang |first5=Xiaomei |last6=Zhou |first6=Zhonghe |title=An Enantiornithine with a Fan-Shaped Tail, and the Evolution of the Rectricial Complex in Early Birds |journal=Current Biology |date=January 2016 |volume=26 |issue=1 |pages=114–119 |doi=10.1016/j.cub.2015.11.036 |pmid=26748849 |doi-access=free }}</ref> Another species of Enantiornithes, ''[[Feitianius]]'', also had an elaborate fan of tail feathers. More importantly, soft tissue preserved around the tail was interpreted as the remains of a rectrical bulb, suggesting that this feature was not in fact restricted to species with modern-looking pygostyles, but might have evolved much earlier than previously thought and been present in many Enantiornithes.<ref name=Feitianius>{{cite journal |last1=O'Connor |first1=Jingmai K. |last2=Li |first2=Da-Qing |last3=Lamanna |first3=Matthew C. |last4=Wang |first4=Min |last5=Harris |first5=Jerald D. |last6=Atterholt |first6=Jessie |last7=You |first7=Hai-Lu |title=A new Early Cretaceous enantiornithine (Aves, Ornithothoraces) from northwestern China with elaborate tail ornamentation |journal=Journal of Vertebrate Paleontology |date=30 December 2015 |volume=36 |issue=1 |pages=e1054035 |doi=10.1080/02724634.2015.1054035 |s2cid=85800831 }}</ref> At least one genus of Enantiornithes, ''[[Cruralispennia]]'', had a modern-looking pygostyle but lacked a tail fan.<ref name=":1" />

==Biology==

===Diet===
[[File:Life reconstruction of enantiornithine birds feeding.jpg|thumb|Life reconstruction of enantiornithine birds feeding (left ''[[Longipteryx]]'', centre ''[[Bohaiornis]]'' and right ''[[Pengornis]]'')]]
Given the wide diversity of skull shape among Enantiornithes, many different dietary specializations must have been present among the group. Some, like ''[[Shenqiornis]]'', had large, robust jaws suitable for eating hard-shelled invertebrates. The short, blunt teeth of ''[[Pengornis]]'' were likely used to feed on soft-bodied arthropods.<ref name=oconnoretal2011skulls/> The strongly hooked talons of [[Bohaiornithidae]] suggest that they were predators of small to medium-sized vertebrates, but their robust teeth instead suggest a diet of hard-shelled animals.<ref name=bohaiornithidae/>

A few specimens preserve actual stomach contents. Unfortunately, none of these preserve the skull, so direct correlation between their known diet and snout/tooth shape cannot be made. ''[[Eoalulavis]]'' was found to have the remains of [[exoskeleton]]s from aquatic [[crustacean]]s preserved in its digestive tract,<ref name="sanzetal1995">{{cite journal |last1=Sanz |first1=José L. |last2=Chiappe |first2=Luis M. |last3=Buscalioni |first3=Angela D. |title=The Osteology of ''Concornis lacustris'' (Aves: Enantiornithes) from the Lower Cretaceous of Spain and a Reexamination of its Phylogenetic Relationships |journal=American Museum Novitates |issue=3133 |pages=1–23 |date=1995 |hdl=2246/3667 }}</ref> and ''[[Enantiophoenix]]'' preserved corpuscles of amber among the fossilized bones, suggesting that this animal fed on tree sap, much like modern [[sapsucker]]s and other birds. The sap would have fossilized and become amber.<ref name="Dalla Vecchia Chiappe2002">{{cite journal |first1=Fabio M. |last1=Dalla Vecchia |first2=Luis M. |last2=Chiappe |year=2003 |title=First avian skeleton from the Mesozoic of northern Gondwana |journal=Journal of Vertebrate Paleontology |volume=22 |issue=4 |pages=856–60 |jstor=4524284 |doi=10.1671/0272-4634(2002)022[0856:FASFTM]2.0.CO;2 |s2cid=130143737 }}</ref> However, more recently it has been suggested that the sap moved post-mortem, hence not representing true stomachal contents. Combined with the putative fish [[pellet (ornithology)|pellets]] of ''[[Piscivorenantiornis]]'' turning out to be fish excrement, the strange stomachal contents of some species turning out to be [[ovaries]] and the supposed gastroliths of ''[[Bohaiornis]]'' being random mineral precipitates, only the ''[[Eoalulavis]]'' displays actual stomach contents.<ref>{{cite journal |last1=O'Connor |first1=Jingmai K. |title=The trophic habits of early birds |journal=Palaeogeography, Palaeoclimatology, Palaeoecology |date=1 January 2019 |volume=513 |pages=178–195 |doi=10.1016/j.palaeo.2018.03.006 |bibcode=2019PPP...513..178O |s2cid=133781513 }}</ref>

A study on paravian digestive systems indicates that known Enantiornithes lacked a crop and a gizzard, didn't use gastroliths and didn't eject pellets. This is considered at odds with the high diversity of diets that their different teeth and skull shapes imply,<ref>{{cite journal |last1=O'Connor |first1=Jingmai K. |last2=Zhou |first2=Zhonghe |last3=Smith |first3=Andrew |title=The evolution of the modern avian digestive system: insights from paravian fossils from the Yanliao and Jehol biotas |journal=Palaeontology |date=6 November 2019 |volume=63 |issue=1 |pages=13–27 |doi=10.1111/pala.12453 |doi-access=free }}</ref> though some modern birds have lost the gizzard and rely solely on strong stomachal acids.<ref>{{cite journal |last1=Houston |first1=David C. |last2=Copsey |first2=J. A. |title=Bone digestion and intestinal morphology of the Bearded Vulture |journal=The Journal of Raptor Research |date=1994 |volume=28 |issue=2 |pages=73–78 |url=https://www.biodiversitylibrary.org/page/51322199 }}</ref>  An example was discovered with what was suspected to be gastroliths in the what would have been the fossil's stomach, re-opening the discussion of the use of gastroliths by Enantiornithes.  X-ray and scanning microscope inspection of the rocks determined that they were actually chalcedony crystals, and not gastroliths.<ref>{{Cite web|date=2021-03-12|title=Short Crystal: Quartz and the Fossilized Bird {{!}} GeoRarities|url=https://georarities.com/2021/03/12/short-crystal-quartz-and-the-fossilized-bird/|access-date=2021-05-06|language=en}}</ref>

[[Longipterygidae]] is the most extensively studied family in terms of diet due to their rather unusual rostral anatomy, with long jaws and few teeth arranged at the jaw ends. They have variously been interpreted as piscivores,<ref>O’Connor, Jingmai K.; Zhou, Zhonghe; Zhang, Fucheng (28 February 2011). "A reappraisal of Boluochia zhengi (Aves: Enantiornithes) and a discussion of intraclade diversity in the Jehol avifauna, China". Journal of Systematic Palaeontology. 9 (1): 51–63. doi:10.1080/14772019.2010.512614. S2CID 84817636.</ref> probers akin to shorebirds<ref>Lianhai Hou; LuisM. Chiappe; Fucheng Zhang; Cheng-Ming Chuong (2004). "New Early Cretaceous fossil from China documents a novel trophic specialization for Mesozoic birds". Naturwissenschaften. 91 (1): 22–25. Bibcode:2004NW.....91...22H. doi:10.1007/s00114-003-0489-1. PMC 4382005. PMID 14740099.</ref> and as arboreal bark-probers.<ref>Morschhauser, E. M.; Varricchio, D.J.; Gao, C.; Liu, J.; Wang, Z.; Cheng, X. & Meng, Q. (2009). "Anatomy of the Early Cretaceous bird Rapaxavis pani, a new species from Liaoning Province, China". Journal of Vertebrate Paleontology. 29 (2): 545–554. doi:10.1671/039.029.0210. S2CID 84643293.</ref> A 2022 study however does find them most likely to be generalistic insectivores (sans possibly ''[[Shengjingornis]]'' due to its larger size, poorly preserved skull and unusual pedal anatomy), being too small for specialised carnivory and herbivory; the atypical rostrum is tentatively speculated to be unrelated to feeding ecology.<ref>{{cite journal | doi=10.1186/s12915-022-01294-3 | title=Diet of Mesozoic toothed birds (Longipterygidae) inferred from quantitative analysis of extant avian diet proxies | year=2022 | last1=Miller | first1=Case Vincent | last2=Pittman | first2=Michael | last3=Wang | first3=Xiaoli | last4=Zheng | first4=Xiaoting | last5=Bright | first5=Jen A. | journal=BMC Biology | volume=20 | issue=1 | page=101 | pmid=35550084 | pmc=9097364 | doi-access=free }}</ref> However a posterior study has found them to be herbivorous, including the presence of [[gymnosperm]] seeds in their digestive system.<ref>O’Connor, J.; Clark, A.; Herrera, F.; Yang, X.; Wang, X.; Zheng, X.; Hu, H.; Zhou, Z. (2024). "Direct evidence of frugivory in the Mesozoic bird Longipteryx contradicts morphological proxies for diet". Current Biology. doi:10.1016/j.cub.2024.08.012.</ref>

[[File:Reconstruction of an avisaurid (e.g., A. darwini).png|thumb|Depiction of ''[[Avisaurus]]'' preying on a prehistoric mammal]]

[[Avisauridae|Avisaurids]] occupied a niche analogous to modern [[birds of prey]], having the ability to lift small prey with their feet in a manner similar to hawks or owls.<ref>Clark AD, Atterholt J, Scannella JB, Carroll N, O’Connor JK (2024) New enantiornithine diversity in the Hell Creek Formation and the functional morphology of the avisaurid tarsometatarsus. PLoS ONE 19(10): e0310686. https://doi.org/10.1371/journal.pone.0310686</ref><ref>{{Cite web |title=Earliest known fossil examples of predatory birds discovered: New species may have hunted like modern hawks and owls |url=https://phys.org/news/2024-10-earliest-fossil-examples-predatory-birds.html |access-date=2024-10-12 |website=phys.org |language=en}}</ref>

===Predation===
A fossil from Spain reported by Sanz ''et al.'' in 2001 included the remains of four hatchling skeletons of three different species of Enantiornithes. They are substantially complete, very tightly associated, and show surface pitting of the bones that indicates partial digestion. The authors concluded that this association was a regurgitated pellet and, from the details of the digestion and the size, that the hatchlings were swallowed whole by a [[pterosaur]] or small [[theropod]] dinosaur. This was the first evidence that [[Mesozoic]] avialans were prey animals, and that some Mesozoic [[Pan-Aves|pan-avian]]s regurgitated pellets like owls do today.<ref name="Sanzetal2001">{{cite journal |first1=José L. |last1=Sanz |first2=Luis M. |last2=Chiappe |first3=Yolanda |last3=Fernádez-Jalvo |first4=Francisco |last4=Ortega |first5=Begoña |last5=Sánchez-Chillón |first6=Francisco J. |last6=Poyato-Ariza1 |first7=Bernardino P. |last7=Pérez-Moreno |date=February 2001 |title=An early Cretaceous pellet |journal=Nature |volume=409 |issue=6823 |pages=998–1000 |pmid=11234054 |doi=10.1038/35059172|bibcode=2001Natur.409..998S |s2cid=663531 }}</ref>

===Life history===
[[File:Gobipteryx sp eggs.JPG|thumb|left|Fossilized eggs of ''[[Gobipteryx minuta]]'', [[Dinosaurium]] (Prague)]]
Known fossils of Enantiornithes include [[Egg (biology)|eggs]],<ref>{{cite journal |last1=Mikhailov |first1=Konstantin E. |year=1991 |title=Classification of fossil eggshells of amniotic vertebrates |journal=Acta Palaeontologica Polonica |volume=36 |issue=2 |pages=193–238 |url=https://www.app.pan.pl/archive/published/app36/app36-193.pdf }}</ref><ref>{{cite journal |last1=Mikhailov |first1=Konstantin E. |year=1996 |title=New Genera of Fossil Eggs from the Upper Cretaceous of Mongolia |journal=Paleontological Journal |volume=30 |issue=2 |pages=246–8}}</ref> [[embryo]]s,<ref>{{cite journal |last1=Elżanowski |first1=Andrzej |author-link=Andrzej Elżanowski |year=1981 |title=Embryonic bird skeletons from the late Cretaceous of Mongolia |journal=Palaeontologia Polonica |volume=42 |pages=147–79 |url=http://www.palaeontologia.pan.pl/Archive/1981-42_147-179_40-45.pdf }}</ref> and [[hatchling]]s.<ref>{{cite journal |first1=José L. |last1=Sanz |first2=Luis M. |last2=Chiappe |first3=Bernardino P. |last3=Pérez-Moreno |first4=José J. |last4=Moratalla |first5=Francisco |last5=Hernández-Carrasquilla |first6=Angela D. |last6=Buscalioni |first7=Francisco |last7=Ortega |first8=Francisco J. |last8=Poyato-Ariza |first9=Diego |last9=Rasskin-Gutman |first10=Xavier |last10=Martı́nez-Delclòs |date=June 6, 1997 |title=A Nestling Bird from the Lower Cretaceous of Spain: Implications for Avian Skull and Neck Evolution |journal=Science |volume=276 |issue=5318 |pages=1543–6 |doi=10.1126/science.276.5318.1543}}</ref> An embryo, still curled in its egg, has been reported from the [[Yixian Formation]].<ref>{{cite journal |first1=Zhonghe |last1=Zhou |first2=Fucheng |last2=Zhang |date=October 22, 2004 |title=A Precocial Avian Embryo from the Lower Cretaceous of China |journal=Science |volume=306 |issue=5696 |pages=653 |doi=10.1126/science.1100000 |pmid=15499011 |s2cid=34504916 }}</ref> Juvenile specimens can be identified by a combination of factors: rough texture of their bone tips indicating portions which were still made of cartilage at the time of death, relatively small breastbones, large skulls and eyes, and bones which had not yet fused to one another.<ref name="chiappeetaljuveniles">{{cite journal|last1=Chiappe|first1=Luis M.|last2=Shu'an|first2=Ji|last3=Qiang|first3=Ji|year=2007|title=Juvenile Birds from the Early Cretaceous of China: Implications for Enantiornithine Ontogeny|journal=American Museum Novitates|issue=3594|pages=1–46|doi=10.1206/0003-0082(2007)3594[1:JBFTEC]2.0.CO;2|hdl=2246/5890|s2cid=85871695 |url=https://www.biodiversitylibrary.org/bibliography/169246}}</ref> Some hatchling specimens have been given formal names, including "''[[Liaoxiornis delicatus]]''"; however, [[Luis Chiappe]] and colleagues considered the practice of naming new species based on juveniles detrimental to the study of Enantiornithes, because it is nearly impossible to determine which adult species a given juvenile specimen belongs to, making any species with a hatchling holotype a ''[[nomen dubium]]''.<ref name=chiappeetaljuveniles/>

Together with hatchling specimens of the Mongolian ''[[Gobipteryx]]''<ref>{{cite journal |last1=Elżanowski |first1=Andrzej |year=1995 |title=Cretaceous birds and avian phylogeny |journal=Courier Forschungsinstitut Senckenberg |volume=181 |pages=37–53}}</ref> and ''[[Gobipipus]]'',<ref name="gobipipus_desc">{{cite journal |last1=Kurochkin |first1=E. N. |last2=Chatterjee |first2=S. |last3=Mikhailov |first3=K. E. |title=An embryonic enantiornithine bird and associated eggs from the cretaceous of Mongolia |journal=Paleontological Journal |date=December 2013 |volume=47 |issue=11 |pages=1252–1269 |doi=10.1134/S0031030113110087 |bibcode=2013PalJ...47.1252K |s2cid=86747842 }}</ref><ref>{{cite journal |last1=Kurochkin |first1=E. N. |last2=Chatterjee |first2=S. |last3=Mikhailov |first3=K. E. |title=An embryonic enantiornithine bird and associated eggs from the cretaceous of Mongolia |journal=Paleontological Journal |date=19 December 2013 |volume=47 |issue=11 |pages=1252–1269 |doi=10.1134/S0031030113110087 |bibcode=2013PalJ...47.1252K |s2cid=86747842 }}</ref> these finds demonstrate that hatchling Enantiornithes had the skeletal ossification, well-developed wing feathers, and large brain which correlate with [[precocial]] or [[superprecocial]] patterns of development in birds of today. In other words, Enantiornithes probably hatched from the egg already well developed and ready to run, forage, and possibly even fly at just a few days old.<ref name=chiappeetaljuveniles/>

Findings suggests Enantiornithes, especially the toothed species, had a longer incubation time than modern birds.<ref>[https://www.pnas.org/doi/full/10.1073/pnas.1613716114 Dinosaur incubation periods directly determined from growth-line counts in embryonic teeth show reptilian-grade development - PNAS]</ref><ref>[https://royalsocietypublishing.org/doi/10.1098/rsbl.2018.0090 The origin of the bird's beak: new insights from dinosaur incubation periods]</ref>

Analyses of Enantiornithes bone histology have been conducted to determine the growth rates of these animals. A 2006 study of ''[[Concornis]]'' bones showed a growth pattern different from modern birds; although growth was rapid for a few weeks after hatching, probably until [[fledging]], this small species did not reach adult size for a long time, probably several years.<ref name="cambra-mooetal2006">{{cite journal |first1=Oscar |last1=Cambra-Moo |first2=Ángela Delgado |last2=Buscalioni |first3=Jorge |last3=Cubo |first4=Jacques |last4=Castanet |first5=Marie-Madeleine |last5=Loth |first6=Emmanuel |last6=de Margerie |first7=Armand |last7=de Ricqlès |year=2006 |title=Histological observations of Enantiornithine bone (Saurischia, Aves) from the Lower Cretaceous of Las Hoyas (Spain) |journal=Comptes Rendus Palevol |volume=5 |issue=5 |pages=685–91 |doi=10.1016/j.crpv.2005.12.018 |bibcode=2006CRPal...5..685C }}</ref> Other studies have all supported the view that growth to adult size was slow, as it is in living precocial birds (as opposed to [[altricial]] birds, which are known to reach adult size quickly).<ref name="sanzetal1995"/> Studies of the rate of bone growth in a variety of Enantiornithes has shown that smaller species tended to grow faster than larger ones, the opposite of the pattern seen in more primitive species like ''[[Jeholornis]]'' and in non-avialan dinosaurs.<ref>{{cite journal |first1=Jingmai K. |last1=O'Connor |first2=Min |last2=Wang |first3=Xiao-Ting |last3=Zheng |first4=Xiao-Li |last4=Wang |first5=Zhong-He |last5=Zhou |year=2014 |url=http://www.ivpp.cas.cn/cbw/gjzdwxb/xbwzxz/201401/P020140121384211870999.pdf |title=The histology of two female Early Cretaceous birds |journal=Vertebrata PalAsiatica |volume=52 |issue=1 |pages=112–28 }}</ref> Some analyses have interpreted the bone histology to indicate that Enantiornithes may not have had fully avian [[endotherm]]y, instead having an intermediate [[metabolic rate]].<ref>{{cite journal |last1=Chiappe |first1=L.M. |year=1995 |title=The phylogenetic position of the Cretaceous birds of Argentina: Enantiornithes and ''Patagopteryx deferrariisi'' |journal=Courier Forschungsinstitut Senckenberg |volume=181 |pages=55–63 }}</ref> However a 2021 study rejects the idea that they had less endothermic metabolisms than modern birds.<ref>{{Cite journal|url=https://onlinelibrary.wiley.com/doi/10.1111/pala.12583|doi=10.1111/pala.12583|title=Palaeohistological inferences of resting metabolic rates in Concornis and Iberomesornis (Enantiornithes, Ornithothoraces) from the Lower Cretaceous of las Hoyas (Spain)|year=2021|last1=Cubo|first1=Jorge|last2=Buscalioni|first2=Angela D.|last3=Legendre|first3=Lucas J.|last4=Bourdon|first4=Estelle|last5=Sanz|first5=Jose L.|last6=Ricqlès|first6=Armand|journal=Palaeontology|volume=65 |s2cid=245082389}}</ref>

Evidence of colonial nesting has been found in Enantiornithes, in sediments from the [[Late Cretaceous]] ([[Maastrichtian]]) of [[Romania]].<ref>{{cite journal |first1=Gareth |last1=Dyke |first2=Mátyás |last2=Vremir |first3=Gary |last3=Kaiser |first4=Darren |last4=Naish |date=June 2012  |title=A drowned Mesozoic bird breeding colony from the Late Cretaceous of Transylvania |journal=Die Naturwissenschaften |volume=99 |issue=6 |pages=435–42 |pmid=22575918 |doi=10.1007/s00114-012-0917-1 |bibcode=2012NW.....99..435D |citeseerx=10.1.1.394.9006 |s2cid=1396792 }}</ref> Evidence from nesting sites shows that Enantiornithes buried their eggs like modern [[megapodes]], which is consistent with their inferred superprecocial adaptations.<ref>{{cite journal |last1=Fernández |first1=Mariela S. |last2=García |first2=Rodolfo A. |last3=Fiorelli |first3=Lucas |last4=Scolaro |first4=Alejandro |last5=Salvador |first5=Rodrigo B. |last6=Cotaro |first6=Carlos N. |last7=Kaiser |first7=Gary W. |last8=Dyke |first8=Gareth J. |last9=Farke |first9=Andrew A. |title=A Large Accumulation of Avian Eggs from the Late Cretaceous of Patagonia (Argentina) Reveals a Novel Nesting Strategy in Mesozoic Birds |journal=PLOS ONE |date=17 April 2013 |volume=8 |issue=4 |pages=e61030 |doi=10.1371/journal.pone.0061030 |pmid=23613776 |pmc=3629076 |bibcode=2013PLoSO...861030F |doi-access=free }}</ref>

A 2020 study on a juvenile's feathers further stresses the ontological similarities to modern megapodes, but cautions several differences such as the arboreal nature of most Enantiornithes as opposed to the terrestrial lifestyle of megapodes.<ref>{{cite journal |last1=O'Connor |first1=Jingmai K. |last2=Falk |first2=Amanda |last3=Wang |first3=Min |last4=Zheng |first4=Xiao-Ting |title=First report of immature feathers in juvenile Enantiornithes from the Early Cretaceous Jehol avifauna |journal=Vertebrata PalAsiatica |volume=58 |year=2020 |pages=24–44 |doi=10.19615/j.cnki.1000-3118.190823 }}</ref>

It has been speculated that superprecociality in Enantiornithes might have prevented them from developing specialised toe arrangements seen in modern birds like zygodactyly.<ref>{{cite journal |last1=Clark |first1=Alexander D. |last2=O'Connor |first2=Jingmai K. |title=Exploring the Ecomorphology of Two Cretaceous Enantiornithines With Unique Pedal Morphology |journal=Frontiers in Ecology and Evolution |date=15 June 2021 |volume=9 |pages=654156 |doi=10.3389/fevo.2021.654156 |doi-access=free }}</ref>

Although the vast majority of histology studies and known remains of Enantiornithes point to superprecociality being the norm, one specimen, MPCM-LH-26189, seems to represent an altricial juvenile, implying that like modern birds Enantiornithes explored multiple reproductive strategies.<ref>{{cite journal |last1=Kaye |first1=Thomas G. |last2=Pittman |first2=Michael |last3=Marugán-Lobón |first3=Jesús |last4=Martín-Abad |first4=Hugo |last5=Sanz |first5=José Luis |last6=Buscalioni |first6=Angela D. |title=Fully fledged enantiornithine hatchling revealed by Laser-Stimulated Fluorescence supports precocial nesting behavior |journal=Scientific Reports |date=21 March 2019 |volume=9 |issue=1 |pages=5006 |doi=10.1038/s41598-019-41423-7 |pmid=30899080 |pmc=6428842 |bibcode=2019NatSR...9.5006K }}</ref>

===Flight===
Because many Enantiornithes lacked complex tails and possessed radically different wing anatomy compared to modern birds, they have been the subject of several studies testing their flight capabilities.

Traditionally, they have been considered inferior flyers, due to the shoulder girdle anatomy being assumed to be more primitive and unable to support a ground-based launching mechanism,<ref>{{cite journal |last1=Padian |first1=Kevin |last2=Chiappe |first2=Luis M. |title=The origin and early evolution of birds |journal=Biological Reviews |date=11 January 2007 |volume=73 |issue=1 |pages=1–42 |doi=10.1111/j.1469-185x.1997.tb00024.x |s2cid=86007060 |url=http://doc.rero.ch/record/16121/files/PAL_E3214.pdf }}</ref> as well as due to the absence of [[rectrice]]s in many species.<ref name="Clarkeetal2006"/><ref name=hongshan2014>{{cite journal |first1=Luis M. |last1=Chiappe |first2=Zhao |last2=Bo |first3=Jingmai K. |last3=O'Connor |first4=Gao |last4=Chunling |first5=Wang |last5=Xuri |first6=Michael |last6=Habib |first7=Jesus |last7=Marugan-Lobon |first8=Meng |last8=Qingjin |first9=Cheng |last9=Xiaodong |year=2014 |title=A new specimen of the Early Cretaceous bird ''Hongshanornis longicresta'': insights into the aerodynamics and diet of a basal ornithuromorph |journal=PeerJ |volume=2 |pages=e234 |pmid=24482756 |pmc=3898307 |doi=10.7717/peerj.234  |doi-access=free }}</ref><ref name=Schizooura>{{cite journal |first1=Shuang |last1=Zhou |first2=Zhong-He |last2=Zhou |first3=Jingmai K. |last3=O'Connor |year=2012 |title=A new basal beaked ornithurine bird from the Lower Cretaceous of Western Liaoning, China |journal=Vertebrata PalAsiatica |volume=50 |issue=1 |pages=9–24 |url=http://www.ivpp.cas.cn/cbw/gjzdwxb/xbwzxz/201202/P020120209570168040733.pdf}}
*{{cite web |date=February 13, 2012 |title=New basal beaked ornithurine bird found from the lower cretaceous of Western Liaoning, China |website=Phys.org |url=http://phys.org/news/2012-02-basal-beaked-ornithurine-bird-cretaceous.html}}</ref>

However, several studies have shown that they were efficient flyers, like modern birds, possessing a similarly complex nervous system and wing feather ligaments. Additionally, the lack of a complex tail appears to not have been very relevant for [[Bird flight|avian flight]] as a whole - some extinct birds like [[Lithornithidae|lithornids]] also lacked complex tail feathers but were good flyers,<ref>Houde, Peter W. (1988). "Paleognathous Birds from the Early Tertiary of the Northern Hemisphere". Publications of the Nuttall Ornithological Club (Cambridge Massachusetts, USA: Nuttall Ornithological Club) 22</ref> and they appear to have been capable of a ground based launching.<ref>{{cite journal |last1=Navalón |first1=Guillermo |last2=Marugán-Lobón |first2=Jesús |last3=Chiappe |first3=Luis M. |last4=Luis Sanz |first4=José |last5=Buscalioni |first5=Ángela D. |title=Soft-tissue and dermal arrangement in the wing of an Early Cretaceous bird: Implications for the evolution of avian flight |journal=Scientific Reports |date=6 October 2015 |volume=5 |issue=1 |pages=14864 |doi=10.1038/srep14864 |pmid=26440221 |pmc=4594305 |bibcode=2015NatSR...514864N }}</ref>

Enantiornithes resemble [[Ornithuromorph]]s in many anatomical features of the flight apparatus, but a sternal keel is absent in the basal-most members, only a single basal taxon appears to have had a triosseal canal, and their robust [[pygostyle]] seems unable to support the muscles that control the modern tail feathers involved in flight.<ref>{{cite journal |last1=Brusatte |first1=Stephen L. |last2=O'Connor |first2=Jingmai K. |last3=Jarvis |first3=Erich D. |title=The Origin and Diversification of Birds |journal=Current Biology |date=5 October 2015 |volume=25 |issue=19 |pages=R888–898 |doi=10.1016/j.cub.2015.08.003 |pmid=26439352 |s2cid=3099017 |issn=1879-0445|doi-access=free |bibcode=2015CBio...25.R888B |hdl=10161/11144 |hdl-access=free }}</ref> Though some basal Enantiornithes exhibit ancestral flight apparatuses, by the end of the Mesozoic many Enantiornithes had several features convergent with the Neornithes including a deeply keeled sternum, a narrow [[furcula]] with a short hypocleidium, and ulnar quill knobs that indicate increased aerial abilities.<ref>{{cite journal |last1=Atterholt |first1=Jessie |last2=Hutchison |first2=J. Howard |last3=O'Connor |first3=Jingmai K. |title=The most complete enantiornithine from North America and a phylogenetic analysis of the Avisauridae |journal=PeerJ |date=2018 |volume=6 |pages=e5910 |doi=10.7717/peerj.5910 |pmid=30479894 |pmc=6238772 |issn=2167-8359 |doi-access=free }}</ref><ref>{{cite journal |last1=Wang |first1=Xia |last2=McGowan |first2=Alistair J. |last3=Dyke |first3=Gareth J. |last4=Turvey |first4=Samuel T. |title=Avian Wing Proportions and Flight Styles: First Step towards Predicting the Flight Modes of Mesozoic Birds |journal=PLOS ONE |date=7 December 2011 |volume=6 |issue=12 |pages=e28672 |doi=10.1371/journal.pone.0028672 |pmid=22163324 |bibcode=2011PLoSO...628672W |pmc=3233598 |doi-access=free }}</ref>

At least ''[[Elsornis]]'' appears to have become secondarily [[Flightless bird|flightless]].<ref>{{cite journal |last1=Chiappe |first1=Luis M. |last2=Suzuki |first2=Shigeru |last3=Dyke |first3=Gareth J. |last4=Watabe |first4=Mahito |last5=Tsogtbaatar |first5=K. |last6=Barsbold |first6=Rinchen |title=A new Enantiornithine bird from the Late Cretaceous of the Gobi desert |journal=Journal of Systematic Palaeontology |date=January 2007 |volume=5 |issue=2 |pages=193–208 |doi=10.1017/S1477201906001969 |bibcode=2007JSPal...5..193C |s2cid=85391743 }}</ref>

==Classification==
Some researchers classify Enantiornithes, along with the true birds, in the class [[Aves]]. Others use the more restrictive [[crown group]] definition of Aves (which only includes [[neornithes]], anatomically modern birds), and place Enantiornithes in the more inclusive group [[Avialae]]. Enantiornithes were more advanced than ''[[Archaeopteryx]]'', ''[[Confuciusornis]]'', and ''[[Sapeornis]]'', but in several respects they were more primitive than modern birds, perhaps following an intermediate evolutionary path.

A consensus of scientific analyses indicates that Enantiornithes is one of two major groups within the larger group [[Ornithothoraces]]. The other ornithothoracine group is [[Euornithes]] or [[Ornithuromorpha]], which includes all living birds as a subset. This means that Enantiornithes were a successful branch of avialan evolution, but one that diversified entirely separately from the lineage leading to modern birds.<ref name="chiappe&walker2002"/> One study has however found that the shared sternal anatomy was acquired independently and such a relationship needs to be reexamined.<ref>{{cite journal |last1=Zheng |first1=Xiaoting |last2=Wang |first2=Xiaoli |last3=O'Connor |first3=Jingmai |last4=Zhou |first4=Zhonghe |title=Insight into the early evolution of the avian sternum from juvenile enantiornithines |journal=Nature Communications |date=9 October 2012 |volume=3 |issue=1 |pages=1116 |doi=10.1038/ncomms2104 |pmid=23047674 |bibcode=2012NatCo...3.1116Z |doi-access=free }}</ref>

Enantiornithes classification and taxonomy has historically been complicated by a number of factors. In 2010, paleontologists [[Jingmai O'Connor]] and [[Gareth J. Dyke|Gareth Dyke]] outlined a number of criticisms against the prevailing practices of scientists failing to describe many specimens in enough detail for others to evaluate thoroughly. Some species have been described based on specimens which are held in private collections, making further study or review of previous findings impossible. Because it is often unfeasible for other scientists to study each specimen in person given the worldwide distribution of the Enantiornithes, and due to the many uninformative descriptions which have been published on possibly important specimens, many of these specimens become "functional ''[[Nomen dubium|nomina dubia]]''".<ref name=oconnor2010cathayornis>{{cite journal |last1=O'Connor |first1=Jingmai |last2=Dyke |first2=Gareth |year=2010 |title=A Reassessment of ''Sinornis santensis'' and ''Cathayornis yandica'' (Aves: Enantiornithes) |journal=Records of the Australian Museum |volume=62 |pages=7–20 |doi=10.3853/j.0067-1975.62.2010.1540 |url=https://zenodo.org/record/4676605 |doi-access=free }}</ref> Furthermore, many species have been named based on extremely fragmentary specimens, which would not be very informative scientifically even if they were described sufficiently. Over one-third of all named species are based on only a fragment of a single bone. O'Connor and Dyke argued that while these specimens can help expand knowledge of the time span or geographic range of the Enantiornithes and it is important to describe them, naming such specimens is "unjustifiable".<ref name=oconnor2010cathayornis/>

===Relationships===
Enantiornithes is the sister group to [[Euornithes]], and together they form a [[clade]] called [[Ornithothoraces]] (though see above). Most [[phylogenetic]] studies have recovered Enantiornithes as a monophyletic group distinct from the modern birds and their closest relatives. The 2002 phylogenetic analysis by Clarke and Norell, though, reduced the number of Enantiornithes [[autapomorph]]ies to just four.<ref name="clarke&norell2002">{{cite journal |first1=Julia A. |last1=Clarke |first2=Mark A. |last2=Norell |year=2002 |title=The Morphology and Phylogenetic Position of ''Apsaravis ukhaana'' from the Late Cretaceous of Mongolia |journal=American Museum Novitates |issue=3387 |pages=1–46 |doi=10.1206/0003-0082(2002)387<0001:TMAPPO>2.0.CO;2 |citeseerx=10.1.1.693.8475 |s2cid=52971055 }}</ref>

Enantiornithes systematics are highly provisional and notoriously difficult to study, due to their small size<ref name=Carvalhoetal2015/> and the fact that Enantiornithes tend to be extremely [[Homoplasy|homoplastic]], or very similar to each other in most of their skeletal features due to convergent evolution rather than common ancestry.<ref name=chiappeavis/> What appears fairly certain by now is that there were subdivisions within Enantiornithes possibly including some minor basal lineages in addition to the more advanced Euenantiornithes. The details of the interrelationship of all these lineages, indeed the validity of most, is disputed, although the Avisauridae, for one example, seem likely to constitute a valid group. [[Phylogenetic taxonomy|Phylogenetic taxonomists]] have hitherto been very reluctant to suggest delimitations of clades of Enantiornithes.<ref name="sereno(2005)">Sereno, P.C. (2005) ''[http://www.taxonsearch.org/dev/file_home.php TaxonSearch: Stem Archosauria] {{webarchive|url=https://web.archive.org/web/20070219102659/http://www.taxonsearch.org/dev/file_home.php |date=2007-02-19 }}''. Version 1.0, 2005-NOV- 7. Retrieved 2006-OCT-02.</ref>

One such delineation named the '''Euenantiornithes''', was defined by Chiappe (2002) as comprising all species closer to ''[[Sinornis]]'' than to ''[[Iberomesornis]]''. Because ''Iberomesornis'' is often found to be the most primitive or basal member of the Enantiornithes,  Euenantiornithes may be an extremely inclusive group, made up of all Enantiornithes except for ''Iberomesornis'' itself. Despite being in accordance with [[phylogenetic nomenclature]], this definition of Euenantiornithes was severely criticized by some researchers, such as [[Paul Sereno]], who called it "a ill-defined [[clade]] [...] a good example of a poor choice in a phylogenetic definition".<ref name="sereno(2005)"/>

The [[Cladistics#Cladograms|cladogram]] below was found by an analysis by Wang ''et al.'' in 2015, updated from a previous data set created by Jingmai O'Connor.<ref name=Pterygornis/>
{{clade| style=font-size:90%;line-height:90%
|label1=[[Ornithothoraces]]
  |1={{clade
    |1=[[Euornithes]] [[File:Y_martini.png|60px]]
    |label2=†'''Enantiornithes'''
    |2={{clade
          |1=†''[[Protopteryx]]'' [[File:Protopteryx_Silhouette.png|60px]]
          |2=†[[Pengornithidae]] [[File:Chiappeavis_magnapremaxillo.png|60px]]
          |3=†[[Longipterygidae]] [[File:Longipteryx_restoration.jpg|60px]]
          |label4=†'''Euenantiornithes'''
          |4={{clade
           |1=†''[[Eocathayornis]]''
           |2={{clade
              |1=†''[[Elsornis]]''
              |2={{clade
                 |1=†''[[Dunhuangia]]''
                 |2=†''[[Fortunguavis]]''
                 |3={{clade
                    |1=†[[Bohaiornithidae]] [[File:Zhouornis_hani.png|60px]]
                    |2={{clade
                       |1=†''[[Pterygornis]]''
                       |2={{clade
                          |1=†''[[Eoenantiornis]]''[[File:Eoenantiornis-Paleozoological_Museum_of_China.jpg|60px]]
                          |2={{clade
                             |1=†''[[Cathayornis]]''[[File:Cathayornis-Beijing_Museum_of_Natural_History.jpg|60px]]
                             |2={{clade
                               |1=†''[[Vescornis]]''
                               |2=†''[[Neuquenornis]]''
                               |3=†''[[Gobipteryx]]'' [[File:Gobipteryx_reconstruction.jpg|60px]]
                               |4=†''[[Eoalulavis]]''[[File:Eoaluavis_life_restoration.png|60px]]
                                   |5={{clade
                                   |1=†''[[Qiliania]]''
                                   |2=†''[[Concornis]]''[[File:Concornis_lacustris_34.jpg|60px]] }} }} }} }} }} }} }} }} }} }} }} }}

The cladogram below is from Wang ''et al.'', 2022, and includes most named taxa and recovers several previously-named clades. Letters on branches indicate the positions of "wildcard" taxa, those which have been recovered in multiple disparate positions.<ref>{{Cite journal |last1=Wang |first1=Xuri |last2=Cau |first2=Andrea |last3=Luo |first3=Xiaoling |last4=Kundrát |first4=Martin |last5=Wu |first5=Wensheng |last6=Ju |first6=Shubin |last7=Guo |first7=Zhen |last8=Liu |first8=Yichuan |last9=Ji |first9=Qiang |date=2022-02-11 |title=A new bohaiornithid-like bird from the Lower Cretaceous of China fills a gap in enantiornithine disparity |journal=Journal of Paleontology |volume=96 |issue=4 |language=en |pages=961–976 |doi=10.1017/jpa.2022.12 |bibcode=2022JPal...96..961W |s2cid=247432530 |issn=0022-3360|doi-access=free }}</ref>

{{clade| style=font-size:90%;line-height:90%
|label1=Enantiornithes
|sublabel1=''l''
|1={{clade
 |1=''[[Cruralispennia]]''
 |2={{clade
  |1=''[[Protopteryx]]''
  |2={{clade
   |1={{clade
    |1=''[[Elsornis]]''
    |2=''[[Flexomornis]]'' }}
   |2={{clade
    |label1=[[Longipterygidae]]
    |1={{clade
     |1=''[[Iberomesornis]]''
     |label2=''bh''
     |2={{clade
      |label1=''bh''
      |1=''[[Longirostravis]]''
      |2=''[[Rapaxavis]]'' }} }}
    |label2=[[Euenantiornithes]]
    |2={{clade
     |label1=''c''
     |1={{clade
      |label1=''e''
      |1=''[[Sinornis]]''
      |label2=''e''
      |2={{clade
       |1=''[[Enantiornis]]''
       |2={{clade
        |1=''[[Halimornis]]''
        |2={{clade
         |1=''[[Concornis]]''
         |2=''[[Neuquenornis]]'' }} }} }}
      |label3=''c''
      |3={{clade
       |label1=''b''
       |1={{clade
        |1=''[[Eoalulavis]]''
        |2=''[[Liaoningornis]]'' }}
       |2={{clade
        |1=''[[Gobipteryx]]''
        |2=''[[Hebeiornis]]'' }} }} }}
     |2={{clade
      |1=''[[Eocathayornis]]''
      |2={{clade
       |1={{clade
        |1=''[[Qiliania]]''
        |label2=[[Avisauridae]]
        |sublabel2=''e''
        |2={{clade
         |1={{clade
          |1=''[[Intiornis]]''
          |2=''[[Soroavisaurus]]'' }}
         |2={{clade
          |1=''[[Avisaurus]]''
          |2={{clade
           |1=''[[Gettyia]]''
           |label2=''n''
           |2=''[[Mirarce]]'' }} }} }} }}
       |2={{clade
        |1=''[[Feitianius]]''
        |2={{clade
         |1={{clade
          |label1=''fn''
          |1=''[[Longusunguis]]''
          |label2=''fn''
          |2={{clade
           |label1=''n''
           |1=''[[Dunhuangia]]''
           |label2=''fn''
           |2=''[[Musivavis]]'' }} }}
         |2={{clade
          |label1=[[Pengornithidae]]
          |sublabel1=''m''
          |1={{clade
           |1=''[[Pengornis]]''
           |label2=''m''
           |2={{clade
            |1=''[[Yuanchuavis]]''
            |2={{clade
             |1=''[[Eopengornis]]''
             |2=''[[Parapengornis]]'' }} }} }}
          |2={{clade
           |1={{clade
            |1=''[[Grabauornis]]''
            |2={{clade
             |1=''[[Parvavis]]''
             |2={{clade
              |1=''[[Cratoavis]]''
              |2=''[[Gretcheniao]]'' }} }} }}
           |2={{clade
            |1={{clade
             |1=''[[Huoshanornis]]''
             |2=''[[Shengjingornis]]'' }}
            |2={{clade
             |1=''[[Zhouornis]]''
             |label2=[[Bohaiornithidae]]
             |2={{clade
              |1=''[[Bohaiornis]]''
              |label2=''ij''
              |2={{clade
               |1=''[[Eoenantiornis]]''
               |2={{clade
                |1=''[[Fortunguavis]]''
                |2={{clade
                 |1=''[[Mystiornis]]''
                 |2={{clade
                  |1=''[[Shenqiornis]]''
                  |2=''[[Sulcavis]]''
}} }} }} }} }} }} }} }} }} }} }} }} }} }} }} }} }} }} }}

Key to letters:

''b'' = ''[[Boluochia]]''<br>
''c'' = ''[[Cathayornis]]''<br>
''e'' = ''[[Enantiophoenix]]''<br>
''f'' = ''[[Houornis]]''<br>
''h'' = ''[[Longipteryx]]''<br>
''i'' = ''[[Parabohaiornis]]''<br>
''j'' = ''[[Pterygornis]]''<br>
''l'' = ''[[Vorona]]''<br>
''m'' = ''[[Yuanjiawaornis]]''<br>
''n'' = ''[[Yungavolucris]]''

== List of genera ==

=== [[Incertae sedis]] ===
Enantiornithes taxonomy is difficult to evaluate, and as a result few clades within the group are consistently found by phylogenetic analyses. Most Enantiornithes are not included in any specific family, and as such are listed here. Many of these have been considered Euenantiornithes, although the controversy behind this name means that it is not used consistently in studies of Enantiornithes.{{citation needed|date=March 2021}}

{| class="wikitable sortable" align="center" width="100%"
|-
! Name
! Year
! Formation
! Location
! Notes
! Images
|-
|''[[Abavornis]]''
| [[1998 in paleontology|1998]]
| [[Bissekty Formation]] ([[Late Cretaceous]], [[Turonian]] to [[Coniacian]])
| {{flag|Uzbekistan}}
| One of many fragmentary Bissekty Enantiornithes, known only from [[coracoid]]s
|
|-
|''[[Alethoalaornis]]''
| [[2007 in paleontology|2007]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Poorly known
|
|-
|''[[Alexornis]]''
| [[1976 in paleontology|1976]]
| [[La Bocana Roja Formation]] ([[Late Cretaceous]], [[Campanian]])
| {{flag|Mexico}}
| One of the first Enantiornithes known. Once thought to be an ancient relative of [[Coraciidae|rollers]] and [[woodpeckers]]
| [[File:Alexornis antecedens.png|200px]]
|-
|''[[Avimaia]]''
| [[2019 in paleontology|2019]]
| [[Xiagou Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| One specimen from this genus died with an unlaid egg in its body
| [[File:Fossil-AvimaiaSchweitzeraeWithUnlaidEgg.jpg|200px]]
|-
|''[[Bauxitornis]]''
| [[2010 in paleontology|2010]]
| [[Csehbánya Formation]] ([[Late Cretaceous]], [[Santonian]])
| {{flag|Hungary}}
| Fragmentary but unique in the structure of its tarsometatarsus
| [[File:Bauxitornis.jpg|200px]]
|-
|''[[Brevirostruavis]]''
| [[2021 in paleontology|2021]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Possessed an enlarged [[hyoid]] that suggests a feeding specialization similar to hummingbirds, honeyeaters, and woodpeckers
|[[File:Brevirostruavis macrohyoideus restoration by Lauren Helton.png|frameless]]
|-
|''[[Castignovolucris]]''
| [[2023 in paleontology|2023]]
| Unnamed formation ([[Late Cretaceous]], [[Campanian]])
| {{flag|France}}
| May have been the size of a [[Canada goose]]
|
|-
|''[[Catenoleimus]]''
| [[1998 in paleontology|1998]]
| [[Bissekty Formation]] ([[Late Cretaceous]], [[Turonian]] to [[Coniacian]])
| {{flag|Uzbekistan}}
| One of many fragmentary Bissekty Enantiornithes, known only from a [[coracoid]]
|
|-
|''[[Cathayornis]]''
| [[1992 in paleontology|1992]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| One of the first Jehol biota Enantiornithes described. Known from many species, although some are now placed into their own genera. May have had a similar appearance and lifestyle to a [[pitta]]
| [[File:Cathayornis - early cretaceous Liaoning IMG 5191 Beijing Museum of Natural History.jpg|200px]]
|-
|''[[Concornis]]''
| [[1992 in paleontology|1992]]
| [[Las Hoyas]] ([[Early Cretaceous]], [[Barremian]])
| {{flag|Spain}}
| One of the most complete Las Hoyas Enantiornithes
| [[File:Concornis lacustris 438.jpg|200px]]
|-
|''[[Cratoavis]]''<ref name= Cratoavis>{{cite journal | last1 = Carvalho | last2 = Novas | last3 = Agnolín | last4 = Isasi | last5 = Freitas | last6 = Andrade | year = 2015 | title = A new genus and species of enantiornithine bird from the Early Cretaceous of Brazil | journal = Brazilian Journal of Geology | volume = 45 | issue = 2| pages = 161–171 | doi=10.1590/23174889201500020001| doi-access = free }}</ref>
| [[2015 in paleontology|2015]]
| [[Santana Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|Brazil}}
| A very well-preserved South American member of the group, complete with ribbon-like tail feathers
| 
|-
|''[[Cruralispennia]]''<ref name=":1">{{Cite journal|last1=Wang|first1=Min|last2=O'Connor|first2=Jingmai K.|last3=Pan|first3=Yanhong|last4=Zhou|first4=Zhonghe|date=2017-01-31|title=A bizarre Early Cretaceous enantiornithine bird with unique crural feathers and an ornithuromorph plough-shaped pygostyle|journal=Nature Communications|language=En|volume=8|pages=14141|doi=10.1038/ncomms14141|pmid=28139644|pmc=5290326|bibcode=2017NatCo...814141W}}</ref>
| [[2017 in paleontology|2017]]
| [[Huajiying Formation]] ([[Early Cretaceous]], [[Hauterivian]])
| {{flag|China}}
| Had an unusual ornithuromorph-like pygostyle and brush-like thigh feathers. One of the oldest Enantiornithes
| [[File:Ncomms14141-f1.jpg|200px]]
|-
|''[[Cuspirostrisornis]]''
| [[1997 in paleontology|1997]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Originally mistakenly believed to have possessed a pointed beak
|[[File:Cuspirostrornis houi life restoration.jpg|frameless]]
|-
|''[[Dalingheornis]]''
| [[2006 in paleontology|2006]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Was well-adapted for climbing due to its [[Bird feet and legs#Toe arrangements|heterodactyl feet]], like those of a [[trogon]]
| 
|-
|''[[Dunhuangia]]''<ref name=dunhuangia>{{cite journal | last1 = Wang | first1 = Li | last2 = O'Connor | first2 = Zhou | last3 = You | year = 2015 | title = Second species of enantiornithine bird from the Lower Cretaceous Changma Basin, northwestern China with implications for the taxonomic diversity of the Changma avifauna | journal = Cretaceous Research | volume = 55 | pages = 56–65 | doi=10.1016/j.cretres.2015.01.008| bibcode = 2015CrRes..55...56W }}</ref>
| [[2015 in paleontology|2015]]
| [[Xiagou Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| A genus of Enantiornithes from the Changma basin, an area which is unusually dominated by ornithuromorphs
| 
|-
|''[[Elbretornis]]''
| [[2009 in paleontology|2009]]
| [[Lecho Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
| {{flag|Argentina}}
| Only known from wing bones. May be synonymous with other Lecho formation Enantiornithes
| 
|-
|''[[Elektorornis]]''
| [[2019 in paleontology|2019]]
|[[Burmese amber|Burmese Amber]] ([[Late Cretaceous]], [[Cenomanian]])
| {{flag|Myanmar}}
| Known from a foot preserved in amber with an elongated middle toe
| 
|-
|''[[Enantiornis]]''
| [[1981 in paleontology|1981]]
| [[Lecho Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
| {{flag|Argentina}}
| Although only known from a few bones, this genus is the namesake of Enantiornithes. It was also one of the largest and last representative of the group prior to their extinction
| 
|-
|''[[Eoalulavis]]''
| [[1996 in paleontology|1996]]
| [[Las Hoyas]] ([[Early Cretaceous]], [[Barremian]])
| {{flag|Spain}}
| Preserves feathers including an [[alula]], a specialized type of feather which controls air flow over the wing
| 
|-
|''[[Eocathayornis]]''
| [[2002 in paleontology|2002]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Once considered to be a basal close relative of ''[[Cathayornis]]'', although now considered to be more distantly related
| 
|-
|''[[Eoenantiornis]]''
| [[1999 in paleontology|1999]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Well-preserved but inconsistent in phylogenetic placement
| [[File:Eoenantiornis-Paleozoological Museum of China.jpg|200px]]
|-
|''[[Evgenavis]]''
| [[2014 in paleontology|2014]]
| [[Ilek Formation]] ([[Early Cretaceous]], [[Barremian]])
| {{flag|Russia}}
| Known only from a tarsometatarsus which shares some features with those of Enantiornithes
| 
|-
|''[[Explorornis]]''
| [[1998 in paleontology|1998]]
| [[Bissekty Formation]] ([[Late Cretaceous]], [[Turonian]] to [[Coniacian]])
| {{flag|Uzbekistan}}
| One of many fragmentary Bissekty Enantiornithes, known only from [[coracoid]]s
|
|-
|''[[Falcatakely]]''
| [[2020 in paleontology|2020]]
| [[Maevarano Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
| {{flag|Madagascar}}
| Developed a massive snout with only a single tooth, despite retaining a "primitive" skull arrangement in contrast to modern birds
| [[File:Falcatakely restoration.jpg|200px]]
|-
|''[[Feitianius]]''<ref name="Feitianius"/>
| [[2015 in paleontology|2015]]
| [[Xiagou Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Possessed an elaborate set of tail feathers, unlike the paired ribbon-like feathers of most Enantiornithes
|[[file:feitianius paradisi.jpg|200px]]
|-
|''[[Flexomornis]]''
| [[2010 in paleontology|2010]]
| [[Woodbine Formation]] ([[Late Cretaceous]], [[Cenomanian]])
| {{flag|United States}} ({{flag|Texas}}) 
| One of the oldest North American avialans found, albeit known only from fragmentary remains
|
|-
| ''[[Fortipesavis]]''
| [[2021 in paleontology|2021]]
| [[Burmese amber]] ([[Late Cretaceous]], [[Cenomanian]])
| {{flag|Myanmar}}
| Had an enlarged outer toe that may have been an adaptation for perching
|
|-
|''[[Fortunguavis]]''<ref name=fortunguavis>{{cite journal | last1 = Wang | first1 = M. | last2 = O'Connor | first2 = J. K. | last3 = Zhou | first3 = Z. | year = 2014 | title = A new robust enantiornithine bird from the Lower Cretaceous of China with scansorial adaptations | journal = Journal of Vertebrate Paleontology | volume = 34 | issue = 3| pages = 657–671 | doi=10.1080/02724634.2013.812101| bibcode = 2014JVPal..34..657W | s2cid = 85313872 }}</ref>
| [[2014 in paleontology|2014]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Had robust bones, including feet and claws which may have been adapted for climbing trees
|
|-
|''[[Grabauornis]]''<ref>{{cite journal | last1 = Dalsätt | first1 = J. | last2 = Ericson | first2 = P. G. | last3 = Zhou | first3 = Z. | year = 2015 | title = A New Enantiornithes (Aves) from the Early Cretaceous of China | doi = 10.1111/1755-6724.12270 | journal = Acta Geologica Sinica | volume = 86 | issue = 2| pages = 801–807 | s2cid = 131170912 }}</ref>
| [[2015 in paleontology|2015]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Barremian]])
| {{flag|China}}
| The proportions of the wings of this genus of Enantiornithes as well as the presence of an alula suggest that it was a good flier
|
|-
|''[[Gracilornis]]''
| [[2011 in paleontology|2011]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| A possible relative of ''Cathayornis'' with characteristically slender bones
|
|-
|''[[Gurilynia]]''
| [[1999 in paleontology|1999]]
| [[Nemegt Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
| {{flag|Mongolia}}
| A poorly known genus of Enantiornithes, but evidently a large and late-surviving member of the group
|
|-
|''[[Hollanda luceria|Hollanda]]''<ref name=hollanda>{{cite journal |last1=Bell |first1=Alyssa K. |last2=Chiappe |first2=Luis M. |last3=Erickson |first3=Gregory M. |last4=Suzuki |first4=Shigeru |last5=Watabe |first5=Mahito |last6=Barsbold |first6=Rinchen |last7=Tsogtbaatar |first7=K. |title=Description and ecologic analysis of Hollanda luceria, a Late Cretaceous bird from the Gobi Desert (Mongolia) |journal=Cretaceous Research |date=February 2010 |volume=31 |issue=1 |pages=16–26 |doi=10.1016/j.cretres.2009.09.001 |bibcode=2010CrRes..31...16B }}</ref>
| [[2010 in paleontology|2010]]
| [[Barun Goyot Formation]] ([[Late Cretaceous]], [[Campanian]])
| {{flag|Mongolia}}
| Originally identified as an ornithuromorph but since reinterpreted as a genus of Enantiornithes closely related to ''[[Lectavis]]''.<ref>{{cite journal |last1=Hartman |first1=Scott |last2=Mortimer |first2=Mickey |last3=Wahl |first3=William R. |last4=Lomax |first4=Dean R. |last5=Lippincott |first5=Jessica |last6=Lovelace |first6=David M. |title=A new paravian dinosaur from the Late Jurassic of North America supports a late acquisition of avian flight |journal=PeerJ |date=10 July 2019 |volume=7 |pages=e7247 |doi=10.7717/peerj.7247 |pmid=31333906 |pmc=6626525 |doi-access=free }}</ref>
| [[File:Hollanda luceria 2021.jpg|200px]]
|-
|''[[Holbotia]]''<ref name=holbotia>{{cite journal |last1=Zelenkov |first1=Nikita V. |last2=Averianov |first2=Alexander O. |title=A historical specimen of enantiornithine bird from the Early Cretaceous of Mongolia representing a new taxon with a specialized neck morphology |journal=Journal of Systematic Palaeontology |date=13 June 2015 |volume=14 |issue=4 |pages=319–338 |doi=10.1080/14772019.2015.1051146 |s2cid=85784633 }}</ref>
| [[2015 in paleontology|2015]]
| [[Andaikhudag Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|Mongolia}}
| Considered a small [[pterosaur]] since its discovery in 1977 until it received a formal description in 2015. Possessed unique neck vertebrae and a primitive palate
|
|-
|''[[Houornis]]''
| [[1997 in paleontology|1997]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Once considered to be dubious or a species of ''Cathayornis'', although a 2015 study considered it to be a valid genus<ref name=cathayornithidae2015>{{Cite journal | doi = 10.1080/14772019.2014.994087| title = Taxonomical reappraisal of Cathayornithidae (Aves: Enantiornithes)| journal = Journal of Systematic Palaeontology| volume = 14| pages = 1–19| year = 2015| last1 = Wang | first1 = M. | last2 = Liu | first2 = D. | s2cid = 86665059}}</ref>
|
|-
|''[[Huoshanornis]]''
| [[2010 in paleontology|2010]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| May have been a very maneuverable flier due to the structure of its hand and sternum
|
|-
|''[[Iberomesornis]]''
| [[1992 in paleontology|1992]]
| [[Las Hoyas]] ([[Early Cretaceous]], [[Barremian]])
| {{flag|Spain}}
| One of the first genera of Enantiornithes known from decent remains. Also one of the oldest and most primitive members of the group
| [[File:Iberomesornis-model.jpg|200px]]
|-
|''[[Imparavis]]''<ref name="Imparavis">{{Cite journal |last1=Wang |first1=Xiaoli |last2=Clark |first2=Alexander D. |last3=O'Connor |first3=Jingmai K. |last4=Zhang |first4=Xiangyu |last5=Wang |first5=Xing |last6=Zheng |first6=Xiaoting |last7=Zhou |first7=Zhonghe |date=2024-02-27 |title=First Edentulous Enantiornithine (Aves: Ornithothoraces) from the Lower Cretaceous Jehol Avifauna |url=https://www.sciencedirect.com/science/article/pii/S0195667124000405 |journal=[[Cretaceous Research]] |volume=159 |issue=in press |pages=105867 |doi=10.1016/j.cretres.2024.105867 |issn=0195-6671}}</ref>
|[[2024 in archosaur paleontology|2024]]
|[[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
|{{flag|China}}
|The earliest known enantiornithine with a toothless beak
|
|-
|''[[Incolornis]]''
| [[1998 in paleontology|1998]]
| [[Bissekty Formation]] ([[Late Cretaceous]], [[Turonian]] to [[Coniacian]])
| {{flag|Uzbekistan}}
| One of many fragmentary Bissekty Enantiornithes, known only from [[coracoid]]s. One species was once considered to belong to ''Enantiornis''
|
|-
|''[[Junornis]]''<ref>{{cite journal |last1=Liu |first1=Di |last2=Chiappe |first2=Luis M. |last3=Serrano |first3=Francisco |last4=Habib |first4=Michael |last5=Zhang |first5=Yuguang |last6=Meng |first6=Qinjing |last7=Shawkey |first7=Matthew |title=Flight aerodynamics in enantiornithines: Information from a new Chinese Early Cretaceous bird |journal=PLOS ONE |date=11 October 2017 |volume=12 |issue=10 |pages=e0184637 |doi=10.1371/journal.pone.0184637 |pmid=29020077 |pmc=5636078 |bibcode=2017PLoSO..1284637L |doi-access=free }}</ref>
| [[2017 in paleontology|2017]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| So well preserved that its flight pattern could be reconstructed using the proportions of its feathers and wings
| [[File:Junornis.PNG|200px]]
|-
|''[[Kizylkumavis]]''
| [[1984 in paleontology|1984]]
| [[Bissekty Formation]] ([[Late Cretaceous]], [[Turonian]] to [[Coniacian]])
| {{flag|Uzbekistan}}
| One of the many fragmentary Bissekty Enantiornithes, known only from a [[humerus]] fragment
| [[File:Kizylkumavis cretacea.jpg|200px]]
|-
|''[[Largirostrornis]]''
| [[1997 in paleontology|1997]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Possibly related to ''Cuspirostrisornis'' or a synonym of ''Cathayornis''
|
|-
|''[[Lectavis]]''
| [[1993 in paleontology|1993]]
| [[Lecho Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
| {{flag|Argentina}}
| A large and long-legged member of the group, proportionally similar to modern shorebirds
|[[File:Lectavis bretincola reconstruction by Lauren Helton.jpg|center|frameless]]
|-
|''[[Lenesornis]]''
| [[1996 in paleontology|1996]]
| [[Bissekty Formation]] ([[Late Cretaceous]], [[Turonian]] to [[Coniacian]])
| {{flag|Uzbekistan}}
| One of many fragmentary Bissekty Enantiornithes, known only from a [[synsacrum]] fragment. Originally considered to belong to ''[[Ichthyornis]]''
|
|-
|''[[Liaoningornis]]''
| [[1996 in paleontology|1996]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Originally believed to be an ornithuran, but now considered a relative of ''Eoalulavis''
|
|-
|''[[Longchengornis]]''
| [[1997 in paleontology|1997]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| May have been a synonym of ''Cathayornis''
|
|-
|''[[Magnusavis]]''<ref name="Magnusavis">{{Cite journal |last1=Clark |first1=Alexander D. |last2=Atterholt |first2=Jessie |last3=Scannella |first3=John B. |last4=Carroll |first4=Nathan |last5=O'Connor |first5=Jingmai K. |author-link5=Jingmai O'Connor |date=2024-10-09 |editor-last=Pinheiro |editor-first=Felipe Lima |title=New enantiornithine diversity in the Hell Creek Formation and the functional morphology of the avisaurid tarsometatarsus |journal=[[PLOS One]] |language=en |volume=19 |issue=10 |pages=e0310686 |doi=10.1371/journal.pone.0310686 |issn=1932-6203 |pmid=39383133 |doi-access=free|pmc=11463745 }}</ref>
|[[2024 in archosaur paleontology|2024]]
|[[Hell Creek Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
|{{flag|United States}} ({{flag|Montana}})
|A large enantiornithine closely related to avisaurids
|
|-
|''[[Martinavis]]''
| [[2007 in paleontology|2007]]
| [[Grès à Reptiles Formation]], [[Lecho Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
| {{flag|France}} {{flag|Argentina}}
| Although known only from humeri, this genus was large and lived in a broad range
|
|-
|''[[Microenantiornis]]''
| [[2017 in paleontology|2017]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| A small member of the group which possessed several primitive and derived features compared to other Enantiornithes
| 
|-
|''[[Mirusavis]]''
| [[2020 in paleontology|2020]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Barremian]] to [[Aptian]])
| {{flag|China}}
| Holotype was a small osteologically immature female preserved with medullary bone tissue
|
|-
|''[[Monoenantiornis]]''<ref>{{cite journal |last1=Hu |first1=Han |last2=O'Connor |first2=Jingmai K. |title=First species of Enantiornithes from Sihedang elucidates skeletal development in Early Cretaceous enantiornithines |journal=Journal of Systematic Palaeontology |date=14 November 2016 |volume=15 |issue=11 |pages=909–926 |doi=10.1080/14772019.2016.1246111 |s2cid=89551799 }}</ref>
| [[2016 in paleontology|2016]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Known from a juvenile specimen which depicts how various features developed in Enantiornithes as they age
|
|-
|''[[Musivavis]]''
| [[2022 in paleontology|2022]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Most similar to bohaiornithids but also has features of other groups of Enantiornithes
|
|-
|''[[Nanantius]]''
| [[1986 in paleontology|1986]]
| [[Toolebuc Formation]] ([[Early Cretaceous]], [[Albian]])
| {{flag|Australia}}
| Fragmentary, but may have been a seabird because remains from this genus have been found as [[ichthyosaur]] gut content
|
|-
| ''[[Navaornis]]''
| [[2024 in paleontology|2024]]
| [[Adamantina Formation]] ([[Late Cretaceous]], [[Santonian]] to [[Campanian]])
| {{flag|Brazil}}
| The first toothless enantiornithean from South America, known from a three-dimensionally preserved skull
| [[File:Navaornis skull.webp|200px]]
|-
|''[[Noguerornis]]''
| [[1989 in paleontology|1989]]
| [[El Montsec]] ([[Early Cretaceous]], [[Barremian]])
| {{flag|Spain}}
| Preserves impressions of a [[propatagium]], a skin flap on the shoulder which forms part of a wing
|
|-
|''[[Orienantius]]''
| [[2018 in paleontology|2018]]
| [[Huajiying Formation]] ([[Early Cretaceous]], [[Hauterivian]])
| {{flag|China}}
| Many soft tissue details of specimens from this genus were revealed by UV light
|
|-
|''[[Otogornis]]''
| [[1993 in paleontology|1993]]
| [[Yijinholuo Formation]] ([[Early Cretaceous]])
| {{flag|China}}
| Poorly known
|
|-
|''[[Paraprotopteryx]]''
| [[2007 in paleontology|2007]]
| Qiaotou member of the [[Huajiying Formation]] ([[Early Cretaceous]], [[Aptian]]?)
| {{flag|China}}
| Seemingly had four ribbon-like tail feathers instead of only two as in most Enantiornithes
|
|-
|''[[Parvavis]]''<ref>{{cite journal |last1=Wang |first1=Min |last2=Zhou |first2=Zhonghe |last3=Xu |first3=Guanghui |title=The first enantiornithine bird from the Upper Cretaceous of China |journal=Journal of Vertebrate Paleontology |date=7 January 2014 |volume=34 |issue=1 |pages=135–145 |doi=10.1080/02724634.2013.794814 |bibcode=2014JVPal..34..135W |s2cid=85255564 }}</ref>
| [[2014 in paleontology|2014]]
| [[Jiangdihe Formation]] ([[Late Cretaceous]], [[Turonian]] to [[Santonian]])
| {{flag|China}}
| Small but fully mature at the time of its death. One of only a few Chinese Enantiornithes dated to the Late Cretaceous
| [[File:Parvavis.jpg|200px]]
|-
|''[[Piscivorenantiornis]]''<ref>{{cite journal |last1=Wang |first1=Min |last2=Zhou |first2=Zhonghe |title=A morphological study of the first known piscivorous enantiornithine bird from the Early Cretaceous of China |journal=Journal of Vertebrate Paleontology |date=12 April 2017 |volume=37 |issue=2 |pages=e1278702 |doi=10.1080/02724634.2017.1278702 |bibcode=2017JVPal..37E8702W |s2cid=89858642 }}</ref>
| [[2017 in paleontology|2017]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Known from a disarticulated skeleton preserved overlying a piece of stomach content composed of fish bones, which may have been its last meal
|
|-
|''[[Protopteryx]]''
| [[2000 in paleontology|2000]]
| [[Huajiying Formation]] ([[Early Cretaceous]], [[Hauterivian]])
| {{flag|China}}
| One of the oldest and most primitive members of the group
| [[File:Protopteryx_fengningensis_(BMNHC_Ph1060A)_NMNS.jpg|200px]]
|-
|''[[Pterygornis]]''<ref name=Pterygornis>{{cite journal |last1=Wang |first1=Min |last2=Hu |first2=Han |last3=Li |first3=Zhiheng |title=A new small enantiornithine bird from the Jehol Biota, with implications for early evolution of avian skull morphology |journal=Journal of Systematic Palaeontology |date=21 August 2015 |volume=14 |issue=6 |pages=481–497 |doi=10.1080/14772019.2015.1073801 |s2cid=83603202 }}</ref>
| [[2016 in paleontology|2016]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| One disarticulated skeleton from this genus possesses well-preserved bones of the skull, including a quadratojugal
|
|-
|''[[Qiliania]]''
| [[2011 in paleontology|2011]]
| [[Xiagou Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Some of this genus's remains include well-preserved hindlimbs. the species names, ''Q. graffini'', is named after [[Greg Graffin]] from the band [[Bad Religion]]
|
|-
|''[[Sazavis]]''
| [[1989 in paleontology|1989]]
| [[Bissekty Formation]] ([[Late Cretaceous]], [[Turonian]] to [[Coniacian]])
| {{flag|Uzbekistan}}
| One of many fragmentary Bissekty Enantiornithes, known only from a [[tibiotarsus]] (shin bone)
| [[File:Sazavis prisca.png|200px]]
|-
|''[[Shangyang graciles|Shangyang]]''
| [[2019 in paleontology|2019]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Unusually, the premaxillae of this genus were fused
| 
|-
|''[[Sinornis]]''
| [[1992 in paleontology|1992]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| One of the first Jehol biota Enantiornithes described. Similar to ''Cathayornis'' but usually considered to be distinct
| [[File:Sinornis2.jpg|200px]]
|-
|''[[Xiangornis]]''
| [[2012 in paleontology|2012]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| The hand of this genus was similar to that of ornithuromorphs, likely through [[convergent evolution]]. A large member of the group
|
|-
|''[[Yatenavis]]''<ref name="Yatenavis">{{Cite journal |last1=Herrera |first1=Gerardo Álvarez |last2=Agnolín |first2=Federico |last3=Rozadilla |first3=Sebastián |last4=Lo Coco |first4=Gastón E. |last5=Manabe |first5=Makoto |last6=Tsuihiji |first6=Takanobu |last7=Novas |first7=Fernando E. |date=2022-12-16 |title=New enantiornithine bird from the uppermost Cretaceous (Maastrichtian) of southern Patagonia, Argentina |url=https://www.sciencedirect.com/science/article/pii/S0195667122003160 |journal=Cretaceous Research |volume=144 |language=en |pages=105452 |doi=10.1016/j.cretres.2022.105452 |s2cid=254804249 |issn=0195-6671}}</ref>
|[[2022 in archosaur paleontology|2022]]
|[[Chorrillo Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
|{{flag|Argentina}}
|The southernmost known member of Enantiornithes and one of the youngest members of the group
|
|-
|''[[Yuanjiawaornis]]''<ref name= Yuanjiawaornis>{{cite journal |last1=Hu |first1=Dongyu |last2=Liu |first2=Ying |last3=Li |first3=Jinhua |last4=Xu |first4=Xing |last5=Hou |first5=Lianhai |title=Yuanjiawaornis viriosus, gen. et sp. nov., a large enantiornithine bird from the Lower Cretaceous of western Liaoning, China |journal=Cretaceous Research |date=July 2015 |volume=55 |pages=210–219 |doi=10.1016/j.cretres.2015.02.013 |bibcode=2015CrRes..55..210H }}</ref>
| [[2015 in paleontology|2015]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| One of the largest Enantiornithes known from decent remains
|
|-
|''[[Yungavolucris]]''
| [[1993 in paleontology|1993]]
| [[Lecho Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
| {{flag|Argentina}}
| Had a large and unusually wide [[tarsometatarsal]] (ankle bone)
| [[File:Yungavolucris holotype tarsometatarsus.png|200px]]
|-
|''[[Yuornis]]''
|[[2021 in archosaur paleontology|2021]]
|[[Qiupa Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
|{{flag|China}}
|A large, toothless genus of Enantiornithes, one of the most-well preserved members from the Late Cretaceous.
| [[File:Yuornis skull diagram.png|200px]]
|}

===Longipterygidae===
The [[Longipterygidae]] was a family of long-snouted early Cretaceous Enantiornithes, with teeth only at the tips of the snout. They are generally considered to be fairly basal members of the group.<ref name="O'connoretal.2009" />
{| class="wikitable sortable" align="center" width="100%"
|-
! Name
! Year
! Formation
! Location
! Notes
! Images
|-
|''[[Boluochia]]''
| [[1995 in paleontology|1995]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Originally mistakenly believed to have possessed a hooked beak
|
|-
|''[[Camptodontornis]]''
| [[2010 in paleontology|2010]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Originally called ''Camptodontus'', although that genus name is occupied by a [[Camptodontus (beetle)|beetle]]
|
|-
|''[[Dapingfangornis]]''
| [[2006 in paleontology|2006]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| May have had a thornlike structure on its forehead
|
|-
|''[[Longipteryx]]''
| [[2001 in paleontology|2001]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| The most common and well-known member of the family
| [[File:Longipteryx chaoyangensis - early cretaceous Liaoning IMG 5197 Beijing Museum of Natural History.jpg|200px]]
|-
|''[[Longirostravis]]''
| [[2004 in paleontology|2004]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Like other longipterygids, it possessed a thin snout which may have been used for probing for invertebrates in mud or bark
| [[File:Longirostravis-Tianjin Natural History Museum.jpg|200px]]
|-
|''[[Rapaxavis]]''
| [[2009 in paleontology|2009]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Specialized for perching due to the structure of its feet
| [[File:Rapaxavis.jpg|200px]]
|-
|''[[Shanweiniao]]''
| [[2009 in paleontology|2009]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Acquired multiple tail feathers which may have been capable of generating lift as in modern birds
| [[File:Shanweiniao cooperorum.jpg|200px]]
|-
|''[[Shengjingornis]]''
| [[2012 in paleontology|2012]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| A large member of the family
|
|}

===Pengornithidae===
The [[Pengornithidae]] was a family of large early Enantiornithes. They had numerous small teeth and numerous primitive features which are lost in most other Enantiornithes.<ref name=eopengornis/> Mostly known from the early Cretaceous of China, with putative Late Cretaceous taxa from Madagascar.<ref name="O'Connor, P. M. 2020">{{cite journal |last1=O'Connor |first1=Patrick M. |last2=Turner |first2=Alan H. |last3=Groenke |first3=Joseph R. |last4=Felice |first4=Ryan N. |last5=Rogers |first5=Raymond R. |last6=Krause |first6=David W. |last7=Rahantarisoa |first7=Lydia J. |title=Late Cretaceous bird from Madagascar reveals unique development of beaks |journal=Nature |date=10 December 2020 |volume=588 |issue=7837 |pages=272–276 |doi=10.1038/s41586-020-2945-x |pmid=33239782 |bibcode=2020Natur.588..272O |s2cid=227174405 }}</ref>
{| class="wikitable sortable" align="center" width="100%"
|-
! Name
! Year
! Formation
! Location
! Notes
! Images
|-
|''[[Chiappeavis]]''<ref name=chiappeavis/>
| [[2015 in paleontology|2015]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Possessed a fan-shaped tail composed of many feathers
| [[File:Chiappeavis magnapremaxillo.png|200px]]
|-
|''[[Eopengornis]]''
| [[2014 in paleontology|2014]]
| [[Huajiying Formation]] ([[Early Cretaceous]], [[Hauterivian]])
| {{flag|China}}
| The oldest known member of the family, and one of the oldest putative genera of Enantiornithes known. Possessed extremely well-preserved tail ribbons
|
|-
|''[[Parapengornis]]''<ref name=parapengornis>{{cite journal |last1=Hu |first1=Han |last2=O'Connor |first2=Jingmai K. |last3=Zhou |first3=Zhonghe |last4=Farke |first4=Andrew A. |title=A New Species of Pengornithidae (Aves: Enantiornithes) from the Lower Cretaceous of China Suggests a Specialized Scansorial Habitat Previously Unknown in Early Birds |journal=PLOS ONE |date=3 June 2015 |volume=10 |issue=6 |pages=e0126791 |doi=10.1371/journal.pone.0126791 |pmid=26039693 |pmc=4454694 |bibcode=2015PLoSO..1026791H |doi-access=free }}</ref>
| [[2015 in paleontology|2015]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Proposed to have a woodpecker-like lifestyle due to features of the foot and tail
| [[File:Parapengornis holotype.png|200px]]
|-
|''[[Pengornis]]''
| [[2008 in paleontology|2008]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| The first pengornithid discovered, and also one of the largest members of the Enantiornithes known from decent remains
|
|-
|''[[Yuanchuavis]]''
| [[2021 in paleontology|2021]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Possesses an elaborate "pintail" tail fan longer than its body, which may have had a display function
|  [[File: Yuanchuavis kompsosoura.png|200px]]
|}

===Bohaiornithidae===
[[Bohaiornithidae|Bohaiornithids]] were large but geologically short-lived early Enantiornithes, with long, hooked talons and robust teeth with curved tips. They may have been equivalent to birds of prey, although this interpretation is open to much debate.<ref name=bohaiornithidae>{{cite journal |first1=Min |last1=Wang |first2=Zhong-He |last2=Zhou |first3=Jingmai K. |last3=O'Connor |first4=Nikita V. |last4=Zelenkov |year=2014 |url=http://www.ivpp.cas.cn/cbw/gjzdwxb/xbwzxz/201401/P020140121386256443882.pdf |title=A new diverse enantiornithine family (Bohaiornithidae fam. nov.) from the Lower Cretaceous of China with information from two new species |journal=Vertebrata PalAsiatica |volume=52 |issue=1 |pages=31–76}}</ref> The [[monophyly]] of this group is doubtful, and it may actually be an [[evolutionary grade]].<ref>{{cite journal |last1=Chiappe |first1=Luis M. |last2=Qingjin |first2=Meng |last3=Serrano |first3=Francisco |last4=Sigurdsen |first4=Trond |last5=Min |first5=Wang |last6=Bell |first6=Alyssa |last7=Di |first7=Liu |title=New ''Bohaiornis''-like bird from the Early Cretaceous of China: enantiornithine interrelationships and flight performance |journal=PeerJ |date=25 October 2019 |volume=7 |pages=e7846 |doi=10.7717/peerj.7846 |pmid=31667014 |pmc=6816414 |doi-access=free }}</ref>
{| class="wikitable sortable" align="center" width="100%"
|-
! Name
! Year
! Formation
! Location
! Notes
! Images
|-
|''[[Beiguornis]]''
| [[2022 in paleontology|2022]]
| [[Longjiang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Had a short but robust manual ungual
|
|-
|''[[Bohaiornis]]''
| [[2011 in paleontology|2011]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| Originally considered to have been preserved with [[gastroliths]], although later these were found to be mineral concretions
| [[File:Bohaiornis skull reconstruction.png|200px]]
|-
|''[[Gretcheniao]]''
| [[2019 in paleontology|2019]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Barremian]])
| {{flag|China}}
| Adapted for flapping, rather than soaring, flight. Its describers suggest paraphyly or polyphyly of Bohaiornithidae
|[[File:Gretcheniao sinensis holotype.png|200px]]
|-
|''[[Linyiornis]]''<ref name=Linyiornis>{{cite journal |last1=Wang |first1=Yan |last2=Wang |first2=Min |last3=O'Connor |first3=Jingmai K. |last4=Wang |first4=Xiaoli |last5=Zheng |first5=Xiaoting |last6=Zhang |first6=Xiaomei |title=A new Jehol enantiornithine bird with three-dimensional preservation and ovarian follicles |journal=Journal of Vertebrate Paleontology |date=11 January 2016 |volume=36 |issue=2 |pages=e1054496 |doi=10.1080/02724634.2015.1054496 |bibcode=2016JVPal..36E4496W |s2cid=85807045 }}</ref>
| [[2016 in paleontology|2016]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| A possible member of the family, known from a well-preserved skeleton complete with structures believed to be developing eggs
|
|-
|''[[Longusunguis]]''
| [[2014 in paleontology|2014]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| A fairly typical member of the family
| [[File:Longusunguis skull.png|200px]]
|-
|''[[Parabohaiornis]]''
| [[2014 in paleontology|2014]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| A close relative of ''Bohaiornis''
|
|-
|''[[Shenqiornis]]''
| [[2010 in paleontology|2010]]
| Qiaotou member of the [[Huajiying Formation]] ([[Early Cretaceous]], [[Aptian]]?)
| {{flag|China}}
| The first known member of the family, although not considered a close relative of ''Bohaiornis'' until a few years later. Preserves a large postorbital bone
|
|-
|''[[Sulcavis]]''
| [[2013 in paleontology|2013]]
| [[Yixian Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| A close relative of ''Shenqiornis'' with grooved [[Tooth enamel|enamel]] on its teeth, unique among fossil birds
| [[File:Sulcavis skull.png|200px]]
|-
|''[[Zhouornis]]''
| [[2013 in paleontology|2013]]
| [[Jiufotang Formation]] ([[Early Cretaceous]], [[Aptian]])
| {{flag|China}}
| A large member of the family with a well-preserved braincase
| [[File:Zhouornis hani.png|200px]]
|}

===Gobipterygidae===
Some members of the group are obscure or poorly described and may be synonymous with its type species, ''Gobipteryx minuta''.
{| class="wikitable sortable" align="center" width="100%"
|-
! Name
! Year
! Formation
! Location
! Notes
! Images
|-
|''[[Gobipteryx]]''
| [[1974 in paleontology|1974]]
| [[Barun Goyot Formation]] ([[Late Cretaceous]], [[Campanian]])
| {{flag|Mongolia}}
| A toothless advanced genus of Enantiornithes, possessing a robust beak which convergently evolved with those of modern birds
|
|-
|''[[Jibeinia]]''
| [[1997 in paleontology|1997]]
| Qiaotou member of the [[Huajiying Formation]] ([[Early Cretaceous]], [[Aptian]]?)
| {{flag|China}}
| Poorly known and described from a skeleton which has now been lost. May have been synonymous with ''Vescornis''
|
|-
|''[[Vescornis]]''
| [[2004 in paleontology|2004]]
| Qiaotou member of the [[Huajiying Formation]] ([[Early Cretaceous]], [[Aptian]]?)
| {{flag|China}}
| A small and short-snouted genus of Enantiornithes which may be synonymous with ''Jibeinia''
|
|}

===Avisauridae===
[[Avisauridae]] is subjected to two differing definitions of varying inclusiveness. The more inclusive definition, which follows Cau & Arduini (2008), is used here. Avisaurids were a long-lasting and widespread family of Enantiornithes, which are mainly distinguished by specific features of their tarsometatarsals (ankle bones). The largest and most advanced members of the group survived in North and South America up until the end of the Cretaceous, yet are very fragmentary compared to some earlier taxa.
{| class="wikitable sortable" align="center" width="100%"
|-
! Name
! Year
! Formation
! Location
! Notes
! Images
|-
|''[[Avisaurus]]''
| [[1985 in paleontology|1985]]
| [[Hell Creek Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
| {{flag|United States}} ({{flag|Montana}})
| The eponymous avisaurid, as well as one of the largest members of the family. Originally considered a non-avialan dinosaur
| [[File:Avisaurus and Brachychampsa by tomozsaurus.jpg|200px]]
|-
|''[[Elsornis]]''
| [[2007 in paleontology|2007]]
| [[Djadochta Formation]] ([[Late Cretaceous]], [[Campanian]])
| {{flag|Mongolia}}
| Although incomplete, its skeleton possesses three-dimensional preservation. Possibly flightless due to its wing proportions
| 
|-
|''[[Enantiophoenix]]''
| [[2008 in paleontology|2008]]
| [[Ouadi al Gabour Formation]] ([[Late Cretaceous]], [[Cenomanian]])
| {{flag|Lebanon}}
| Was once believed to have fed on tree sap as it was preserved in association with [[amber]] beads, however this was later determined as an artefact of preservation and not an indicator of diet
|
|-
|''[[Gettyia]]''
| [[2018 in paleontology|2018]]
| [[Two Medicine Formation]] ([[Late Cretaceous]], [[Campanian]])
| {{flag|United States}} ({{flag|Montana}})
| A new genus for ''Avisaurus gloriae''
| 
|-
|''[[Halimornis]]''
| [[2002 in paleontology|2002]]
| [[Mooreville Chalk Formation]] ([[Late Cretaceous]], [[Campanian]])
| {{flag|United States}} ({{flag|Alabama}})
| Would have lived in a coastal environment
|
|-
|''[[Intiornis]]''
| [[2010 in paleontology|2010]]
| [[Las Curtiembres Formation]] ([[Late Cretaceous]], [[Campanian]])
| {{flag|Argentina}}
| Although closely related to some of the largest avisaurids, members of this genus were very small birds
| [[File:Intiornis holotype left foot.png|200px]]
|-
|''[[Mirarce]]''
| [[2018 in paleontology|2018]]
| [[Kaiparowits Formation]] ([[Late Cretaceous]], [[Campanian]])
| {{flag|United States}} ({{flag|Utah}})
| The most complete known North American avisaurid
| [[File:Mirarce_eatoni.jpg|200px]]
|-
|''[[Mystiornis]]''
| [[2011 in paleontology|2011]]
| [[Ilek Formation]] ([[Early Cretaceous]], [[Barremian]] to [[Aptian]])
| {{flag|Russia}}
| Possesses a myriad of features from various groups in [[Paraves]], although most closely resembles avisaurids among sampled groups
|
|-
|''[[Neuquenornis]]''
| [[1994 in paleontology|1994]]
| [[Bajo de la Carpa Formation]] ([[Late Cretaceous]], [[Santonian]])
| {{flag|Argentina}}
| Possessed long wings and a reverse hallux, indicating good flight and perching abilities
|
|-
|''[[Soroavisaurus]]''
| [[1993 in paleontology|1993]]
| [[Lecho Formation]] ([[Late Cretaceous]], [[Maastrichtian]])
| {{flag|Argentina}}
| A very close relative of ''Avisaurus''
|
|}

===Dubious genera and notable unnamed specimens===
*''[[Gobipipus reshetovi]]'': Described in 2013 from embryo specimens within eggshells from the [[Barun Goyot Formation]] of [[Mongolia]]. These specimens were very similar to embryonic ''Gobipteryx'' specimens, although the describers of ''Gobipipus'' (a set of controversial paleontologists including [[Evgeny Kurochkin]] and [[Sankar Chatterjee]]) consider it distinct.<ref name=gobipipus>{{cite journal |last1=Kurochkin |first1=E. N. |last2=Chatterjee |first2=S. |last3=Mikhailov |first3=K. E. |title=An embryonic enantiornithine bird and associated eggs from the cretaceous of Mongolia |journal=Paleontological Journal |date=19 December 2013 |volume=47 |issue=11 |pages=1252–1269 |doi=10.1134/s0031030113110087 |bibcode=2013PalJ...47.1252K |s2cid=86747842 }}</ref>
*''[[Hebeiornis]] fengningensis'': A synonym of ''Vescornis'' due to having been described from the same specimen. Despite having been described in 1999, 5 years prior to the description of ''Vescornis'', the description was so poor compared to the description of ''Vescornis'' that the latter name is considered to take priority by most authors. As a result, the name ''Hebeiornis'' is considered a ''[[nomen nudum]]'' ("naked name").
* "[[Proornis]]" is an informally-named bird from North Korea. It may not be a member of Enantiornithes.
* ''[[Liaoxiornis delicatus]]'': Described in 1999 from a specimen of Enantiornithes found in the [[Yixian Formation]]. This specimen was originally considered to be a tiny adult, but later found to be a hatchling. Other specimens have henceforth been assigned to the genus. Due to a lack of distinguishing feature, many paleontologists have considered this genus an undiagnostic ''[[nomen dubium]]''.
* "Wasaibpanchi": A supposed member of Enantiornithes from Pakistan; the describing paper is of dubious status.
*'''LP-4450''': A juvenile of an indeterminate specimen of Enantiornithes from the [[El Montsec]] Formation of [[Spain]]. Its 2006 description studied the [[histology]] of the skeleton, while later studies reported a squamosal bone present in the specimen but unknown in other Enantiornithes.
*'''IVPP V 13939''': Briefly described in 2004, this Yixian Enantiornithes specimen had advanced pennaceous feathers on its legs, similar to (albeit shorter than) those of other paravians such as ''[[Microraptor]]'' and ''[[Anchiornis]]''.<ref name=legfeather />
*'''DIP-V-15100''' and '''DIP-V-15101''': Two different wings from hatchling specimens which were described in 2015. They attracted a significant amount of media attention upon their description. They were preserved in exceptional details due to having been trapped within Burmese amber for approximately 99 million years.<ref name="amber_enant" />
*'''HPG-15-1''': A partial corpse of an Enantiornithes hatchling also preserved in Burmese amber. Although indeterminate, it attracted even more media attention than the two wings upon its description in 2017.<ref name=ambercorpse />
*'''CUGB P1202''': An indeterminate juvenile [[bohaiornithid]] from the [[Jiufotang Formation]]. A 2016 analysis of its feathering found elongated putative [[melanosomes]], suggesting that a large portion of its feathering was [[iridescent]].
*'''DIP-V-15102''': Another corpse of an indeterminate hatchling preserved in Burmese amber. Described in early 2018.<ref name=":0" />
*'''MPCM-LH-26189 a/b''': A partial skeleton of a hatchling from [[Las Hoyas]] in Spain, including both slab and counter-slab components. Its 2018 description revealed how various features developed in Enantiornithes as they aged. Such features include the [[ossification]] of the [[sternum]] from various smaller bones, and the fusion of tail vertebrae into a [[pygostyle]].

== References ==
{{reflist|25em}}

== External links ==
{{Commons category-inline}}

{{Enantiornithes}}
{{Birds}}
{{Taxonbar|from=Q132268}}

[[Category:Enantiornitheans| ]]
[[Category:Ornithothoraces]]
[[Category:Cretaceous birds]]
[[Category:Early Cretaceous first appearances]]
[[Category:Maastrichtian extinctions]]

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Template:Don't edit this line extinct (view source) (template editor protected)
Template:Don't edit this line link target (view source) (template editor protected)
Template:Don't edit this line link text (view source) (template editor protected)
Template:Don't edit this line parent (view source) (template editor protected)
Template:Don't edit this line rank (view source) (template editor protected)
Template:Don't edit this line same as (view source) (template editor protected)
Template:Edit taxonomy (view source) (template editor protected)
Template:Enantiornithes (view source) (semi-protected)
Template:Fix (view source) (protected)
Template:Fix/category (view source) (protected)
Template:Flag (view source) (template editor protected)
Template:Flag/core (view source) (template editor protected)
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Template:Fossil range/bar (view source) (template editor protected)
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Template:Geological range (view source) (template editor protected)
Template:Hlist/styles.css (view source) (protected)
Template:Icon (view source) (template editor protected)
Template:If empty (view source) (protected)
Template:Is italic taxon (view source) (template editor protected)
Template:Lang (view source) (template editor protected)
Template:Main other (view source) (protected)
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Template:Navbox (view source) (template editor protected)
Template:Navbox with collapsible groups (view source) (template editor protected)
Template:Next period (view source) (template editor protected)
Template:Normal (view source) (template editor protected)
Template:Page needed (view source) (template editor protected)
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Template:Taxobox/Error colour (view source) (template editor protected)
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Template:Taxobox/core/styles.css (view source) (template editor protected)
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Template:Taxonomy/Amniota (view source) (template editor protected)
Template:Taxonomy/Amorphea (view source) (template editor protected)
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Template:Taxonomy/Archosauria (view source) (template editor protected)
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Template:Taxonomy/Averostra (view source) (semi-protected)
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Template:Taxonomy/Bilateria (view source) (template editor protected)
Template:Taxonomy/Choanozoa (edit)
Template:Taxonomy/Chordata (view source) (template editor protected)
Template:Taxonomy/Coelurosauria (view source) (semi-protected)
Template:Taxonomy/Deuterostomia (view source) (template editor protected)
Template:Taxonomy/Dinosauria (view source) (template editor protected)
Template:Taxonomy/Dinosauriformes (view source) (template editor protected)
Template:Taxonomy/Dinosauromorpha (view source) (template editor protected)
Template:Taxonomy/Dracohors (view source) (semi-protected)
Template:Taxonomy/Enantiornithes (view source) (semi-protected)
Template:Taxonomy/Eugnathostomata (view source) (template editor protected)
Template:Taxonomy/Eukaryota (view source) (template editor protected)
Template:Taxonomy/Eukaryota/displayed (view source) (template editor protected)
Template:Taxonomy/Eumetazoa (view source) (template editor protected)
Template:Taxonomy/Filozoa (view source) (template editor protected)
Template:Taxonomy/Gnathostomata (view source) (template editor protected)
Template:Taxonomy/Holozoa (view source) (template editor protected)
Template:Taxonomy/Life (view source) (template editor protected)
Template:Taxonomy/Maniraptora (view source) (semi-protected)
Template:Taxonomy/Maniraptoriformes (view source) (semi-protected)
Template:Taxonomy/Maniraptoromorpha (view source) (semi-protected)
Template:Taxonomy/Neocoelurosauria (edit)
Template:Taxonomy/Neotheropoda (view source) (semi-protected)
Template:Taxonomy/Nephrozoa (view source) (template editor protected)
Template:Taxonomy/Obazoa (view source) (template editor protected)
Template:Taxonomy/Olfactores (view source) (template editor protected)
Template:Taxonomy/Opisthokonta (view source) (template editor protected)
Template:Taxonomy/Orionides (view source) (semi-protected)
Template:Taxonomy/Ornithodira (view source) (template editor protected)
Template:Taxonomy/Ornithothoraces (view source) (semi-protected)
Template:Taxonomy/ParaHoxozoa (view source) (template editor protected)
Template:Taxonomy/Paraves (view source) (semi-protected)
Template:Taxonomy/Pennaraptora (view source) (semi-protected)
Template:Taxonomy/Pygostylia (view source) (semi-protected)
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Template:Taxonomy/Saurischia (view source) (semi-protected)
Template:Taxonomy/Sauropsida (view source) (template editor protected)
Template:Taxonomy/Teleostomi (view source) (template editor protected)
Template:Taxonomy/Tetanurae (view source) (semi-protected)
Template:Taxonomy/Tetrapoda (view source) (template editor protected)
Template:Taxonomy/Theropoda (view source) (semi-protected)
Template:Taxonomy/Tyrannoraptora (view source) (semi-protected)
Template:Taxonomy/Vertebrata (view source) (template editor protected)
Template:Webarchive (view source) (template editor protected)
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Module:Autotaxobox (view source) (template editor protected)
Module:Catalog lookup link (view source) (template editor protected)
Module:Category handler (view source) (protected)
Module:Category handler/blacklist (view source) (protected)
Module:Category handler/config (view source) (protected)
Module:Category handler/data (view source) (protected)
Module:Category handler/shared (view source) (protected)
Module:Check for unknown parameters (view source) (protected)
Module:Citation/CS1 (view source) (protected)
Module:Citation/CS1/COinS (view source) (protected)
Module:Citation/CS1/Configuration (view source) (protected)
Module:Citation/CS1/Date validation (view source) (protected)
Module:Citation/CS1/Identifiers (view source) (protected)
Module:Citation/CS1/Utilities (view source) (protected)
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Module:Clade (view source) (template editor protected)
Module:Commons link (view source) (template editor protected)
Module:DecodeEncode (view source) (template editor protected)
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Module:Disambiguation/templates (view source) (protected)
Module:Exponential search (view source) (template editor protected)
Module:GetParameters (view source) (protected)
Module:Icon (view source) (template editor protected)
Module:Icon/data (view source) (template editor protected)
Module:If empty (view source) (protected)
Module:InfoboxImage (view source) (template editor protected)
Module:Italic title (view source) (template editor protected)
Module:Lang (view source) (template editor protected)
Module:Lang/ISO 639 synonyms (view source) (template editor protected)
Module:Lang/configuration (view source) (template editor protected)
Module:Lang/data (view source) (template editor protected)
Module:Lang/data/iana languages (view source) (template editor protected)
Module:Lang/data/iana regions (view source) (template editor protected)
Module:Lang/data/iana scripts (view source) (template editor protected)
Module:Lang/data/iana suppressed scripts (view source) (template editor protected)
Module:Lang/data/iana variants (view source) (template editor protected)
Module:MultiReplace (view source) (template editor protected)
Module:Namespace detect/config (view source) (protected)
Module:Namespace detect/data (view source) (protected)
Module:Navbar (view source) (protected)
Module:Navbar/configuration (view source) (protected)
Module:Navbar/styles.css (view source) (protected)
Module:Navbox (view source) (template editor protected)
Module:Navbox/configuration (view source) (template editor protected)
Module:Navbox/styles.css (view source) (template editor protected)
Module:Navbox with collapsible groups (view source) (template editor protected)
Module:Navbox with collapsible groups/configuration (view source) (template editor protected)
Module:Pagetype (view source) (protected)
Module:Pagetype/config (view source) (protected)
Module:Pagetype/disambiguation (view source) (protected)
Module:Pagetype/rfd (view source) (protected)
Module:Pagetype/setindex (view source) (protected)
Module:Pagetype/softredirect (view source) (protected)
Module:Plain text (view source) (template editor protected)
Module:ResolveEntityId (view source) (template editor protected)
Module:SDcat (view source) (protected)
Module:String (view source) (protected)
Module:String2 (view source) (template editor protected)
Module:TableTools (view source) (protected)
Module:TaxonItalics (view source) (template editor protected)
Module:Taxonbar (view source) (template editor protected)
Module:Taxonbar/candidate (view source) (template editor protected)
Module:Taxonbar/conf (view source) (template editor protected)
Module:Taxonbar/exists (view source) (template editor protected)
Module:Taxonbar/whitelist (view source) (template editor protected)
Module:Template redirect regex (view source) (template editor protected)
Module:Unicode data (view source) (template editor protected)
Module:Unicode data/scripts (view source) (template editor protected)
Module:Unsubst (view source) (protected)
Module:Webarchive (view source) (template editor protected)
Module:Webarchive/data (view source) (template editor protected)
Module:Wikitext Parsing (view source) (protected)
Module:Yesno (view source) (protected)

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