Basic info | Taxonomic history | Classification | Included Taxa |
Morphology | Ecology and taphonomy | External Literature Search | Age range and collections |
Gastrochaenolites
Taxonomy
Gastrochaenolites was named by Leymerie (1842) [Bivalve borings]. It is considered to be a form taxon.
It was assigned to Ichnofossils by Hantzschel (1975); and to Gastrochaenolitidae by Maisch et al. (2020).
It was assigned to Ichnofossils by Hantzschel (1975); and to Gastrochaenolitidae by Maisch et al. (2020).
Synonyms
|
Synonymy list
Year | Name and author |
---|---|
1842 | Gastrochaenolites Leymerie |
1967 | Paleolithophaga Chiplonkar and Ghare |
1975 | Gastrochaenolites Hantzschel |
2020 | Gastrochaenolites Maisch et al. p. 125 |
Is something missing? Join the Paleobiology Database and enter the data
|
|
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.
G. †Gastrochaenolites Leymerie 1842
show all | hide all
†Gastrochaenolites ampullatus Kelly and Bromley 1984
†Gastrochaenolites cluniformis Kelly and Bromley 1984
†Gastrochaenolites dijugus Kelly and Bromley 1984
†Gastrochaenolites lapidicus Kelly and Bromley 1984
†Gastrochaenolites oelandicus Ekdale and Bromley 2001
†Gastrochaenolites orbicularis Kelly and Bromley 1984
†Gastrochaenolites ornatus Kelly and Bromley 1984
†Gastrochaenolites torpedo Kelly and Bromley 1984
†Gastrochaenolites turbinatus Kelly and Bromley 1984
Invalid names: Paleolithophaga Chiplonkar and Ghare 1967 [synonym]
Diagnosis
Reference | Diagnosis | |
---|---|---|
W. Hantzschel 1975 | Clavate borings in lithic substrates. The apertural region of the boring is narrower than the main chamber and may be circular, oval, or dumb-bell shaped. The aperture may be separated from the main chamber by a neck region which in some cases may be widely flared. The main chamber may vary from subspherical to elongate, having a parabolic to rounded truncated bas and a circular to oval cross section, modified in some forms by a longitudinal ridge or grooves to produce an almond- or heart-shaped section. |
Measurements
No measurements are available
|
|
||||
|
|||||
|
|||||
|
|
||||
Source: g = genus | |||||
Reference: Kelly and Bromley 1984 |
Collections (56 total)
Time interval | Ma | Country or state | Original ID and collection number |
---|---|---|---|
Morrowan | USA (Arkansas) | G. anauchen (10) | |
Hettangian | United Kingdom (Wales) | G. sp. (33356) | |
Planorbis - Liasicus | France | G. sp. (90243) | |
Early/Lower Bajocian | Iran | G. sp. (73966) | |
Discites | United Kingdom | G. lapidicus (141363) | |
Late/Upper Callovian | Israel | G. torpedo (91903) | |
Middle Callovian - Early/Lower Kimmeridgian | Iran (Tabas Area) | G. sp. (41417) | |
Late/Upper Oxfordian | Ethiopia | G. sp. (94339) | |
Middle Oxfordian | Germany (Niedersachsen) | G. dijugus (31435) | |
Middle Oxfordian | France | G. dijugus, G. torpedo (11085) G. lapidicus, G. dijugus, G. orbicularis, G. torpedo (11084) | |
Kimmeridgian | Portugal (Centro) | G. sp. (68220) | |
Early/Lower Kimmeridgian | Switzerland (Jura) | G. sp. (185666) | |
Tithonian | United Kingdom (England) | G. lapidicus (69130) | |
Early/Lower Tithonian | Italy | G. sp. (154046) | |
Early/Lower Hauterivian | Argentina | G. sp. (151914) G. torpedo (61589) | |
Aptian | United Kingdom (England) | G. cluniformis (90691) | |
Late/Upper Aptian | France | G. sp. (56673 58232) | |
Early/Lower Aptian | France | G. sp. (58876) | |
Early/Lower Aptian - Late/Upper Aptian | France | G. sp. (56539) | |
Early/Lower Albian | France | G. sp. (58123 58559) | |
Early/Lower Albian - Late/Upper Albian | France | G. sp. (58861) | |
Late/Upper Albian | Brazil | G. sp. (157868 157869) | |
Late/Upper Albian - Early/Lower Cenomanian | Brazil | G. sp. (157870) | |
Early/Lower Cenomanian | Israel | G. ampullatus (165864) | |
Middle Cenomanian | Belgium | G. orbicularis (90687) | |
Maastrichtian | Mali | G. sp. (114954) | |
Late/Upper Maastrichtian | Netherlands (Limburg) | G. sp. (67134) | |
Late/Upper Maastrichtian | Netherlands | G. lapidicus (138910) | |
Danian | USA (Arkansas) | G. sp. (206776) | |
Danian - Selandian | Argentina (Chubut) | G. sp. (57164) | |
Middle Paleocene - Late/Upper Paleocene | Mali | G. sp. (114964 193687) | |
Ypresian | Mali (Gao) | G. sp. (175262) | |
Aquitanian - Tortonian | Italy (Frosinone) | G. sp. (222634) | |
Burdigalian | Sri Lanka | G. torpedo, G. turbinatus (77478) | |
Burdigalian | France | G. sp. (151413) | |
Middle Miocene | Portugal | G. lapidicus, G. torpedo (151582) G. torpedo (151583 151584) | |
Serravallian | Spain (Catalan) | G. sp. (105064) | |
Early/Lower Pliocene | Spain | G. sp. (153717) G. sp., G. torpedo (153720) | |
Pliocene - Pleistocene | Kenya | G. ampullatus (90690) | |
Pleistocene | United Kingdom (England) | G. ornatus (90686) | |
Calabrian | Cape Verde | G. sp. (176653 176654 176655) G. sp., G. cluniformis (176656) | |
Late/Upper Pleistocene | Italy | G. lapidicus (166071) | |
Late/Upper Pleistocene | Jamaica | G. torpedo (80612) | |
Holocene | Cayman Islands | G. sp. (97605) |