Baissa (PIN collection 3064, bed 32): Aptian, Russian Federation
List of taxa
Where & when
Geology
Taphonomy & methods
Metadata & references
Taxonomic list
Insecta
- Mantodea
- Cretomantidae
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Cretomantis larvalis n. gen., n. sp.
Gratshev and Zherikhin 1993
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1 specimen | |||||||||
PIN 3064/8511 | ||||||||||
Insecta
- Coleoptera
- Carabidae
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Nikolajev 1992 | 1 specimen | |||||||||
PIN 3064/7145 (2 measurements) | ||||||||||
see common names |
Geography
Country: | Russian Federation | State/province: | Buryatia |
Coordinates: | 53.3° North, 112.1° East (view map) | ||
Paleocoordinates: | 50.9° North, 119.4° East (Wright 2013) | ||
Basis of coordinate: | based on nearby landmark | ||
Geographic resolution: | outcrop |
Time
Period: | Cretaceous | Epoch: | Early Cretaceous |
Stage: | Aptian | 10 m.y. bin: | Cretaceous 3 |
Key time interval: | Aptian | ||
Age range of interval: | 121.4 - 113.2 m.y. ago |
Stratigraphy
Formation: | Zaza | ||||
Stratigraphic resolution: | bed | ||||
Stratigraphy comments: C. longipoda, E. trisetalis and Lycoptera all occur in the Zaza Formation indicating that this formation could be correlated with the upper Yixian Formation and the lower Jiufotang Formation in western Liaoning, which have a duration of 122.5-120 Ma. So it is possible to assign the Zaza Formation to an Aptian age. Also correlated with Barremian-Aptian based on plants and pollen. |
Lithology and environment
Primary lithology: | lithified marl | ||
Secondary lithology: | lithified carbonaceous siltstone | ||
Environment: | lacustrine - large | Tectonic setting: | rift |
Geology comments: "The water body is reconstructed as an intermontane lake with the depth of 20 - 30 meters (LYAMINA 1980) situated within a granite massif. The presence of thick layers of the bituminous shales shows that the lake was meromictic, with the oxygen deficiency and high hydrogen sulphur level in the hypolimnion. However, the oxygenated epilimnion should be thick, with a lower boundary well beneath the limit of episodic wave action because no suffocation events are documented. The abundance of caddisflies, dobsonfly larvae and other groups intolerant to oxygen deficiency shows that in more shallow areas the water was clear and well-oxygenated even near the bottom. The lake ecosystem was highly productive as indicated by its complex trophic structure (Fig. 2) with several levels of predators up to the large sturgeon-like fish Stychopterus as well as by the extremely high abundance of planetonivorous phantom midges (SINICHENKOVA & ZHERIKHIN 1996)." ZHERIKHIN et al., 1999 |
Taphonomy
Modes of preservation: | mold/impression |
Size of fossils: | macrofossils |
Collection methods and comments
Collection methods: | survey of museum collection |
Reason for describing collection: | taxonomic analysis |
Museum repositories: | PIN |
Metadata
Database number: | 126065 | ||
Authorizer: | M. Clapham | Enterer: | M. Clapham |
Modifier: | M. Clapham | Research group: | paleoentomology |
Created: | 2012-03-29 10:26:28 | Last modified: | 2025-02-22 15:12:02 |
Access level: | the public | Released: | 2012-03-29 10:26:28 |
Creative Commons license: | CC0 |
Reference information
Primary reference:
8897. | ETE | V. G. Gratshev and V. V. Zherikhin. 1993. New Fossil Mantids (Insecta, Mantida [Sic]). Paleontological Journal 27(1A):148-165 [C. Labandeira/A. Spencer-Lee/M. Clapham] |
Secondary references:
50115 | G. V. Nikolajev. 1992. Taxonomic criteria and generic composition of Mesozoic lamellicorn beetles (Coleoptera, Scarabaeidae). Paleontological Journal 26(1):96-111 [M. Clapham/M. Clapham] |