Journals / Turkish Journal of Earth Sciences / 2014 / Cilt: 23 - Sayı: 2

Santonian-Campanian biostratigraphy of the Kalaat Senan area (West-Central Tunisia)

Pages
184–203
Publication Date
2014-05-18
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

These oceanic conditions appear to have been favorable for radiation of the globotruncanids and heterohelicids.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The Santonian-Campanian (S/C) transition in the Kalaat Senan area is well exposed in the Assila Wadi (OA) section and consists of marls with indurate glauconitic levels towards the base.
📊
Key Findings & Data:This major turnover may have been initiated by an increase in temperatures succeeding a maximum flooding stage of a transgressive period.
💡
Conclusion & Impact:These oceanic conditions appear to have been favorable for radiation of the globotruncanids and heterohelicids.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Santonian/Campanian boundary · biostratigraphy · planktonic foraminifera

Abstract

The Santonian-Campanian (S/C) transition in the Kalaat Senan area is well exposed in the Assila Wadi (OA) section and consists of marls with indurate glauconitic levels towards the base. Standard Mediterranean ammonite biozonations could not be applied to this section because the biomarkers are absent. However, planktonic foraminiferal biozonation is more reliable for indicating the S/C boundary, and here we propose to use the last appearance datum of Dicarinella asymetrica as the index marker of this boundary. A high-resolution quantitative analysis of the planktonic foraminifera of the OA section allows us to define the main bioevents across the S/C transition interval and to specify the S/C boundary. The section reveals that the extinctions across the transition interval occurred among species with a trochospiral keeled test and free portici of the genera Dicarinella and Marginotruncana. In fact, the dicarinellids eventually became extinct and the last appearance of the index species Dicarinella asymetrica defines the S/C boundary, whereas the marginotruncanids suffered a gradual extinction and several species crossed the boundary. Representative taxa of the genera Globotruncanita and Globotruncana first occurred in the uppermost part of the Santonian. These bioevents indicate a major but gradual planktonic foraminiferal turnover during the S/C transition, and may be related to adaptive changes and intraspecific competition. Because dicarinellids and marginotruncanids lived in tropical-subtropical oceanic realms, they seem to have been less able to adapt during the environmental changes associated with the transition; they were progressively replaced by more evolved globotruncanids belonging to the genera Globotruncana and Globotruncanita. This major turnover may have been initiated by an increase in temperatures succeeding a maximum flooding stage of a transgressive period. These oceanic conditions appear to have been favorable for radiation of the globotruncanids and heterohelicids.

Özet

The Santonian-Campanian (S/C) transition in the Kalaat Senan area is well exposed in the Assila Wadi (OA) section and consists of marls with indurate glauconitic levels towards the base. Standard Mediterranean ammonite biozonations could not be applied to this section because the biomarkers are absent. However, planktonic foraminiferal biozonation is more reliable for indicating the S/C boundary, and here we propose to use the last appearance datum of Dicarinella asymetrica as the index marker of this boundary. A high-resolution quantitative analysis of the planktonic foraminifera of the OA section allows us to define the main bioevents across the S/C transition interval and to specify the S/C boundary. The section reveals that the extinctions across the transition interval occurred among species with a trochospiral keeled test and free portici of the genera Dicarinella and Marginotruncana. In fact, the dicarinellids eventually became extinct and the last appearance of the index species Dicarinella asymetrica defines the S/C boundary, whereas the marginotruncanids suffered a gradual extinction and several species crossed the boundary. Representative taxa of the genera Globotruncanita and Globotruncana first occurred in the uppermost part of the Santonian. These bioevents indicate a major but gradual planktonic foraminiferal turnover during the S/C transition, and may be related to adaptive changes and intraspecific competition. Because dicarinellids and marginotruncanids lived in tropical-subtropical oceanic realms, they seem to have been less able to adapt during the environmental changes associated with the transition; they were progressively replaced by more evolved globotruncanids belonging to the genera Globotruncana and Globotruncanita. This major turnover may have been initiated by an increase in temperatures succeeding a maximum flooding stage of a transgressive period. These oceanic conditions appear to have been favorable for radiation of the globotruncanids and heterohelicids.

🔖

Cite This Article

ELAMRI, Z., ZAGHBIB-TURKI, D. (2014). Santonian-Campanian biostratigraphy of the Kalaat Senan area (West-Central Tunisia). Turkish Journal of Earth Sciences, Cilt: 23 - Sayı: 2, 184–203. https://ajindex.com/articles/209906

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (10)

  1. Arenillas I, Arz JA, Molina E, Dupuis C (2000). The Cretaceous boundary at Aïn Settara, Tunisia: sudden catastrophic mass extinction in planktic foraminifera. J Foramin Res 30: 202–218
  2. Arthur MA, Dean WE, Schlanger SO (1985). Variations in the global carbon cycle during the Cretaceous related to climate, volcanism, and changes in atmospheric CO2, In: Sundquist ET and Broecker WS, editors. The Carbon Cycle and Atmospheric CO 2: Natural Variations Archean to Present. Am Geophys Union Geophys Monogr 32: 504–529.
  3. Arz JA (1996). Los foraminíferos planctόnicos del Campaniense y Maastrichtiense: bioestratigrafía, cronoestratigrafía y eventos paleoecolόgicos. PhD, Universidad de Zaragoza, Zaragoza, Spain (in Spanish). Bellier JP (1983). Foraminifères planctoniques du Crétacé de Tunisie septentrionale. Systématique, biozonation, utilisation stratigraphique de l’Albien au Maastrichtien. PhD, Université Pierre et Marie-Curie, Paris, France (in French). Ben Ferjani A, Burollet PF, Mejeri F (1990). Petroleum Geology of Tunisia. ETAP Tunis Mem 1: 1–194.
  4. Berthe D (1949). Log de la série crétacée de Koudiat el Afna-Kalaat es Senam au 5000e. Documents SEREPT, Tunis, GN411 (unpublished; in French). Bey S, Kuss J, Premol Silva I, Negra MH, Gardin S (2012). Faultcontrolled stratigraphy of the late Cretaceous Abiod Formation at Ain Mdheker (Northeast Tunisia). Cretaceous Res 34: 10–25.
  5. Boersma A, Premoli Silva I (1989). Atlantic Paleogene biserial heterohelicid foraminifera and oxygen minima. Paleoceanography 4: 271–286.
  6. Burnett JA (1998). Upper Cretaceous. In: Bown PR, editor. Calcareous Nannofossil Biostratigraphy. Cambridge, UK: Chapman and Hall, pp. 225–265.
  7. Burollet PF (1956). Contribution à l’étude stratigraphique de la Tunisie centrale. Ann Min Geol Tunis 18: 1–350 (in French). Caron M (1985). Cretaceous planktonic foraminifera. In: Bolli HM, Saunders JB, Perch-Nielsen K, editors. Plankton Stratigraphy. Cambridge, UK: Cambridge University Press, pp. 17–86.
  8. Caron M, Homewood P (1982). Evolution of early planktonic foraminifers. Mar Micropaleontol 7: 453–462.
  9. Clarke LG, Jenkyns HC (1999). New oxygen isotope evidence for longterm Cretaceous climatic change in the Southern Hemisphere. Geology 27: 699–702.
  10. Cobban WA, Walaszczyk I, Obradovich JD, Mckinney KC (2006). A USGS zonal table for the Upper Cretaceous middle CenomanianMaastrichtian of the Western Interior of the United States based on ammonites, inoceramids, and radiometric ages. Reston, VA, USA: US Geological Survey