Basic info Taxonomic history Classification Included Taxa
Morphology Ecology and taphonomy External Literature Search Age range and collections

Codiopsis

Echinoidea - Arbacioida - Arbaciidae

Taxonomy
Codiopsis is a genus. It is not extant.

It was assigned to Arbaciidae by Fell and Pawson (1966), Geys (1981), Smith (1995); and to Phymosomatoida by Sepkoski (2002).

Synonymy list
YearName and author
1966Codiopsis Fell and Pawson p. U411
1981Codiopsis Geys p. 258
1995Codiopsis Smith p. 152
2002Codiopsis Sepkoski

Is something missing? Join the Paleobiology Database and enter the data

RankNameAuthor
kingdomAnimalia()
Bilateria
EubilateriaAx 1987
Deuterostomia
Ambulacraria
phylumEchinodermata
subphylumEleutherozoa
RankNameAuthor
Echinozoa()
classEchinoidea()
subclassEuechinoideaBronn 1860
Echinacea()
orderArbacioida()
familyArbaciidae()
genusCodiopsis

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. †Codiopsis
show all | hide all
Codiopsis bruni Lambert 1914
hide
Invalid names: Codiopsis pierrensis Smiser 1935 [synonym]
Codiopsis ciae Lambert 1908
Codiopsis doma Desmarest 1825
Codiopsis lehmannae Smith 1995
Codiopsis stephensoni Cooke 1953
Diagnosis
No diagnoses are available
Measurements
No measurements are available
Composition: high Mg calcitec
Ontogeny: accretion, addition of partsp
Environment: marinep
Locomotion: actively mobilef
Life habit: epifaunalf
Diet: grazerf
Vision: limitedc
Dispersal: waterp
Dispersal 2: planktonicp
Created: 2009-09-10 13:28:35
Modified: 2009-09-10 15:29:25
Source: f = family, c = class, p = phylum
References: Smith 2009, Kiessling 2004, Aberhan 1992

Age range: base of the Valanginian to the top of the Early/Lower Maastrichtian or 137.05000 to 66.00000 Ma

Collections (37 total)


Time interval Ma Country or state Original ID and collection number
Cretaceous143.1 - 66.0Cuba C. ciae (91137)
Valanginian137.05 - 132.6France C. lorini (2222)
Hauterivian132.6 - 125.77Turkmenistan C. lorini (2260)
Hauterivian132.6 - 125.77Morocco (Western High Atlas) C. lorini, C. meslei (2065)
Hauterivian132.6 - 125.77Portugal C. lorini (65749 65853 65854)
Aptian121.4 - 113.2Switzerland C. jaccardi (2189 2226 2228)
Late/Upper Albian - Cenomanian106.3 - 93.9Egypt C. sp. (150677)
Early/Lower Cenomanian - Late/Upper Albian100.5 - 100.5Spain C. doma (3832)
Early/Lower Cenomanian100.5 - 93.9France C. doma (59810 59812 59814)
Early/Lower Cenomanian100.5 - 93.9Egypt C. sp. (140114)
Middle Cenomanian100.5 - 93.9France C. doma (59803 59804 59805)
Middle Cenomanian100.5 - 93.9Serbia C. doma (164671)
Turonian93.9 - 89.8France (Landes) C. arnaudi (213761)
Santonian85.7 - 83.6Spain (Cataluna) C. douvillei (88327)
Santonian85.7 - 83.6Spain C. senessei (66983)
Late/Upper Campanian - Maastrichtian83.6 - 66.0United Arab Emirates C. sp. (67456)
Early/Lower Maastrichtian72.2 - 66.0Spain (Cataluña) C. sp. (67004)
Late/Upper Maastrichtian72.2 - 66.0Belgium (Liege) C. disculus (32157)
Late/Upper Maastrichtian72.2 - 66.0Netherlands (Limburg) C. bruni (3908) C. disculus (32167)
Late/Upper Maastrichtian72.2 - 66.0Netherlands C. bruni (196822 196823 196832 196833) C. pierrensis (196775)
Late/Upper Maastrichtian72.2 - 66.0Belgium C. bruni (196820)
Late/Upper Maastrichtian72.2 - 66.0USA (Texas) C. stephensoni (78102)
Maastrichtian72.2 - 66.0Oman C. sp. (151617)
Late/Upper Maastrichtian - Danian72.2 - 61.66Netherlands C. disculus (32160)