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Permaeschnidae

Insecta - Permaeschnidae

Synonymy list
YearName and author
1931Permaeschnidae Martynov
1932Permaeschnidae Martynov
1992Permaeschnidae Carpenter p. 66
2002Permaeschnidae Huguet et al. p. 541
2007Permaeschnidae Bechly

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RankNameAuthor
kingdomAnimalia()
Bilateria
EubilateriaAx 1987
Protostomia
EcdysozoaAguinaldo et al. 1997
Panarthropoda
phylumArthropodaGravenhorst 1843
Deuteropoda
Mandibulata
PancrustaceaZrzavý and Štys 1997
AltocrustaceaRegier et al. 2010
superclassAllotriocarida
Athalassocarida
LabiocaridaSchwentner et al. 2017
superclassHexapodaLatreille 1825
Cercofilata
classInsecta
Dicondylia
RankNameAuthor
Paranotalia
subclassPterygota()
infraclassHydropalaeopteraRohdendorf 1969
Euhydropalaeoptera
OdonatopteraMartynov 1932
Palaeodonatoptera
Plesiodonatoptera
Apodonatoptera
Paneodonatoptera
Neodonatoptera
Euodonatoptera
OdonatocladaBechly 1999
Nodialata
suborderProtanisoptera
DitaxineuromorphaPritykina 1980
familyPermaeschnidae
familyPermaeschnidae

If no rank is listed, the taxon is considered an unranked clade in modern classifications. Ranks may be repeated or presented in the wrong order because authors working on different parts of the classification may disagree about how to rank taxa.

Fm. †Permaeschnidae Martynov 1931
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G. †Gondvanoptilon Rösler et al. 1981
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Gondvanoptilon brasiliense Rösler et al. 1981
G. †Permaeschna Martynov 1931
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Permaeschna dolloi Martynov 1931
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Invalid names: Permaeschna proxima Martynov 1931 [synonym]
Diagnosis
ReferenceDiagnosis
A. Huguet et al. 2002This family is characterized by the following synapomorphies, after the present phylogenetic analysis (see below): (1) IMA divided into two main branches, the posterior branch being parallel to MP, the anterior branch being parallel to MA, and with secondary branches begin- ning on the posterior branch; (2) RA with a long distal posterior branch; (3) two or more distinctly transverse cells between RP1 and IR2, near the base of IR2; (4) numerous secondary longitudinal veins between RP3/4 and IR2.
The ‘wings large with many cells’ of the Permaeschnidae
is probably a more homoplastic character. The pterostigma basally and distally prolonged is also present in Callimokal- tania martynovi ZALESSKY, 1955, that does not fall in the same clade, after the present phylogenetic analysis (see below). Also, the presence of two or more cross-veins between RP1 and the posterior margin of the pterostigma is a character shared by Hemizygopteron uralense ZA- LESSKY, 1955 and Ditaxineura cellulosa CARPENTER, 1933.
Measurements
No measurements are available
Composition: chitinc
Environment: terrestrialc
Locomotion: actively mobilep
Created: 2017-04-17 09:56:18
Modified: 2017-04-17 09:56:18
Source: c = class, p = phylum
References: Kiessling 2004, Bush and Bambach 2015

Age range: base of the Kungurian to the top of the Changhsingian or 283.30000 to 251.90200 Ma

Collections (4 total)


Time interval Ma Country or state Original ID and collection number
Kungurian283.3 - 274.4Brazil (São Paulo) Gondvanoptilon brasiliense (137840)
Roadian274.4 - 266.9Russian Federation (Arkangelsk) Permaeschna dolloi (104992) Permaeschna dolloi, Permaeschna proxima (104993)
Changhsingian254.14 - 251.902South Africa (Kwazulu-Natal) Permaeschnidae indet. (14350)