Katberg Formation

Last updated
Katberg Formation
Stratigraphic range: Early Triassic
Induan-Olenekian
~252–247  Ma
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Hennie Steyn Bridge over Gariep dam - panoramio.jpg
Hillside overlooking Gariep Dam where Katberg Formation rocks are known
Type Geological formation
Unit of Beaufort Group
Underlies Burgersdorp Formation
Overlies Balfour Formation
Thicknessup to 1,000 m (3,300 ft)
Lithology
Primary Sandstone
Other Mudstone, calcareous concretions
Location
Coordinates 30°30′S26°00′E / 30.5°S 26.0°E / -30.5; 26.0
Region Eastern Cape & Free State
CountryFlag of South Africa.svg  South Africa
Geology of Karoo Supergroup.png

The Katberg Formation is a geological formation that is found in the Beaufort Group, a major geological group that forms part of the greater Karoo Supergroup in South Africa. The Katberg Formation is the lowermost geological formation of the Tarkastad Subgroup which contains the Lower to Middle Triassic-aged rocks of the Beaufort Group. Outcrops and exposures of the Katberg Formation are found east of 24 degrees on wards and north of Graaff-Reniet, Nieu Bethesda, Cradock, Fort Beaufort, Queensdown, and East London in the south, and ranges as far north as Harrismith in deposits that form a ring around the Drakensberg mountain ranges. [1] [2] [3] [4] [5]

Contents

Geology

The Katberg Formation overlies the Balfour Formation of the Adelaide Subgroup and the Burgersdorp Formation of the upper Tarkastad Subgroup, all pertaining to the greater Beaufort Group. The appearance of the Katberg Formation rocks starkly differs from the underlying Balfour Formation due to its high sandstone content and reddish colored mudstones. [6] The high sandstone content of the Katberg Formation, which range from light olive grey, greenish grey, or light brownish grey in color, is a key characteristic of this formation. However, the rocks of the Katberg Formation are differentiated into southern and northern sedimentary facies which grade laterally into one another from the south upwards. The southern and northern Katberg Formation deposits also vary drastically in thickness. [7] [8] [9]

The southern Katberg Formation deposits are the most sandstone-rich, comprising approximately 90 percent sandstone and are fine to medium-grained. Along the coast outcrops and exposures, especially close to East London, the Katberg sandstones are coarse-grained and contain pebbles up to 15 centimetres (5.9 in) in diameter. In the north the sandstones remain consistently fine-grained and exhibit fining upward cycles. The ratio between the sandstones and mudstones grows more equal in the northern deposits, making differentiation between the northern Katberg and Burgersdorp Formations tricky in areas. The Katberg Formation reaches its maximum thickness near East London at 1238m, thinning out gradually northwards. The sandstones are predominantly tabular although exhibit some planar and trough cross-bedding along with horizontal laminations and ripple cross-laminations. The sandstones contain much thinner beds of brownish-red shale and reddish to purple and some minor greenish mudstones, which are frequently structureless or horizontally laminated. Mudstones become redder in colour in the upper Katberg deposits as it grades laterally into the Burgersdorp Formation. Intraformational mud clasts, pedogenic and calcareous nodules are found commonly throughout. [10] [11] [12]

The appearance and proliferation of the sandstone deposits, especially in the southern and lower Katberg Formation, marks the change to an alluvial fan and braided river environment in the Early Triassic due to the presence of coarser-grained sandstones that lack fining upward sequences. Due to the ongoing biotic crises in the aftermath of the Permo-Triassic extinction event, rampant erosion took place as there was a stark drop in plant and animal species diversity. This resulted in unstable ecological niches. The environment at this time was also arid and hot where the rivers seasonally ran dry. When the rainy season arrived, flash floods took place. In the northern Katberg, a drop in the level of preserved sandstones reveals that by the beginning of the Middle Triassic ecosystems were beginning to stabilize after the Permo-Triassic extinction event. The presence of fine-grained sandstones and more plentiful mudstones show that there was a decrease in energy levels in the depositional environment, meaning that the fast flowing braided rivers were steadily replaced by slower flowing, meandering river channels. The environment was still semi-arid, however, due to the presence of the redder mudstones. [13]

Paleontology

The Katberg Formation documents the marked drop in species abundance due to biotic crises that followed the Permo-Triassic extinction event. The most ubiquitous fossils found are different species of Lystrosaurus as the Katberg Formation contains the rocks of the Lystrosaurus Assemblage Zone. The most common fossils found are those of Lystrosaurus murrayi and Lystrosaurus declivis . In the lower Katberg Formation, complete and sometimes mummified articulated skeletons of L. murrayi and L. declivus are found in bone beds containing several individuals. The bone beds are almost always overlain by mudstone infilled with sandstone and capped by other coarse-grained sediments. This provides substantial geological and taphonomical evidence that these Lystrosaurus died near to dried up river channels and were mummified in the arid climate before their remains were buried by flash floods. [14] [15]

The Permo-Triassic extinction event caused the extinction of all gorgonopsians and almost all dicynodont species except for Lystrosaurus and a select few other species such as Myosaurus gracilis . Therocephalian species experience a Lilliput effect where only smaller species survived and thrived after the extinction event. By the upper sections of the biozone, ecological niches began to recover as evidenced by the appearance of new species. Cynodonts experienced the greatest diversification with species such as Thrinaxodon liorhinus and Galesaurus planiceps being found. [16] Small procolonphonid parareptiles such as Owenetta kitchingorum and Procolophon trigoniceps are also found in the Katberg Formation. In addition, the earliest ancestors of Archosauria appear in the lower Katberg Formation.These species are known as archosauromorphs and archosauriformes. Examples of these are Prolacerta broomi and Proterosuchus fergusi respectively. [17] [18] Notably, the Katberg Formation frequently yields burrow casts left by Lystrosaurus . [19]

Correlation

The lower Katberg Formation is known to correspond in age with the Santa Maria Formation of the upper Paraná Basin in southern Brazil. [20]

See also

Related Research Articles

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<span class="mw-page-title-main">Balfour Formation</span> Geological formation in the Beaufort Group of South Africa

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<span class="mw-page-title-main">Teekloof Formation</span> Late Permian geological formation that forms part of the Beaufort Group of South Africa

The Teekloof Formation is a geological formation that forms part of the Beaufort Group, one of the five geological groups that comprises the Karoo Supergroup in South Africa. The Teekloof Formation is the uppermost formation of Adelaide Subgroup deposits West of 24ºE and contains Middle to Late Permian-aged deposits and four biozones of the Beaufort Group. It overlies the Abrahamskraal Formation. The Teekloof Formation does not underlie other units other than the younger Karoo dolerites and sills that relate to the emplacement of the Early Jurassic Drakensberg Group to the east. Outcrops and exposures of the Teekloof Formation range from Sutherland through the mountain escarpments between Fraserburg and Beaufort West. The northernmost localities of the Teekloof Formation are found by Loxton, Victoria West and Richmond.

References

  1. ↑ Broom, R (1906). "V.—On the Permian and Triassic Faunas of South Africa". Geological Magazine. 3 (1): 29–30. Bibcode:1906GeoM....3...29B. doi:10.1017/s001675680012271x. S2CID   129265956.
  2. ↑ Johnson, M. R. (1989-11-01). "Paleogeographic significance of oriented calcareous concretions in the Triassic Katberg Formation, South Africa". Journal of Sedimentary Research. 59 (6): 1008–1010. doi:10.1306/212F90D9-2B24-11D7-8648000102C1865D. ISSN   1527-1404.
  3. ↑ Keyser, A. W., and Smith, R. M. H. (1978). Vertebrate biozonation of the Beaufort Group with special reference to the western Karoo Basin. Geological Survey, Department of Mineral And Energy Affairs, Republic of South Africa.
  4. ↑ Rubidge, B. S. (ed.) 1995b. Biostratigraphy of the Beaufort Group (Karoo Supergroup). South African Committee of Stratigraphy. Biostratigraphic Series 1. Pretoria, Council for Geoscience.
  5. ↑ Viglietti, Pia A. (2012). "Life after extinction: palaeoenvironments of the earliest Triassic lower Katberg formation, including the origin of Lystrosaurus Bonebeds from the Karoo Basin, South Africa". hdl: 11427/11173 .{{cite journal}}: Cite journal requires |journal= (help)
  6. ↑ Viglietti, Pia; Rubidge, Bruce; Malcom Harris Smith, Roger (2017-03-01). "Revised lithostratigraphy of the upper Permian Balfour and Teekloof formations of the main Karoo Basin, South Africa". South African Journal of Geology. 120: 45–60. doi:10.25131/gssajg.120.1.45.
  7. ↑ Kitching, J. W. (1970). A short review of the Beaufort zoning in South Africa. In Second Gondwana Symposium Proceedings and Papers (Vol. 1, pp. 309-312).
  8. ↑ Kitching, J. W. (1977). The distribution of the karroo vertebrate fauna: with special reference to certain genera and the bearing of this distribution on the zoning of the Beaufort Beds, Bernard Price Institute for Palaeontological Research, University of the Witwatersrand.
  9. ↑ Kitching, J. W. (1984). A reassessment of the biozonation of the Beaufort Group. Paleo News, 4(1), 12-13.
  10. ↑ Jirah, Sifelani; McPhee, Blair W.; Viglietti, Pia A.; Bamford, Marion K.; Choiniere, Jonah N.; Hancox, P. John; Barbolini, Natasha; Day, Michael O.; Rubidge, Bruce S. (2016), "Advances in Nonmarine Karoo Biostratigraphy: Significance for Understanding Basin Development", Origin and Evolution of the Cape Mountains and Karoo Basin, Regional Geology Reviews, Springer, Cham, pp. 141–149, doi:10.1007/978-3-319-40859-0_14, ISBN   9783319408583
  11. ↑ O.Catuneanu, H.Wopfner, P.G.Eriksson, B.Cairncross, B.S.Rubidge, R.M.H.Smith, P.J.Hancox (2005-10-01). "The Karoo basins of south-central Africa". Journal of African Earth Sciences. 43 (1–3): 211–253. Bibcode:2005JAfES..43..211C. doi:10.1016/j.jafrearsci.2005.07.007. ISSN   1464-343X.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  12. ↑ Ward, Peter D.; Koch, Paul L.; Smith, Roger M. H.; MacLeod, Kenneth G. (2000-03-01). "Timing of mammal-like reptile extinctions across the Permian-Triassic boundary in South Africa". Geology. 28 (3): 227–230. Bibcode:2000Geo....28..227M. doi:10.1130/0091-7613(2000)28<227:TOMREA>2.0.CO;2. ISSN   0091-7613.
  13. ↑ Smith, R.M.H.,Eriksson, P.G., Botha, W.J. (1993-01-01). "A review of the stratigraphy and sedimentary environments of the Karoo-aged basins of Southern Africa". Journal of African Earth Sciences (and the Middle East). 16 (1–2): 143–169. Bibcode:1993JAfES..16..143S. doi:10.1016/0899-5362(93)90164-L. ISSN   0899-5362.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  14. ↑ Botha, Jennifer; Smith, Roger M. H. (2007-06-01). "Lystrosaurus species composition across the Permo–Triassic boundary in the Karoo Basin of South Africa". Lethaia. 40 (2): 125–137. doi:10.1111/j.1502-3931.2007.00011.x. ISSN   1502-3931.
  15. ↑ Pia A.Viglietti, Roger M.H.Smith, John S.Compton (2013-12-15). "Origin and palaeoenvironmental significance of Lystrosaurus bonebeds in the earliest Triassic Karoo Basin, South Africa". Palaeogeography, Palaeoclimatology, Palaeoecology. 392: 9–21. Bibcode:2013PPP...392....9V. doi:10.1016/j.palaeo.2013.08.015. ISSN   0031-0182.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  16. ↑ Neveling, J., Rubidge, B.S. and Hancox, P.J. (1999-01-01). "A lower Cynognathus Assemblage Zone fossil from the Katberg Formation (Beaufort Group, South Africa)". www.researchgate.net.{{cite web}}: CS1 maint: multiple names: authors list (link)
  17. ↑ Ruta, Marcello; Angielczyk, Kenneth D.; Huttenlocker, Adam K.; Codron, Daryl; Botha-Brink, Jennifer (2016-04-05). "Breeding Young as a Survival Strategy during Earth's Greatest Mass Extinction". Scientific Reports. 6: 24053. doi:10.1038/srep24053. ISSN   2045-2322. PMC   4820772 . PMID   27044713.
  18. ↑ Sues, Hans-Dieter; Modesto, Sean P. (2004-03-01). "The skull of the Early Triassic archosauromorph reptile Prolacerta broomi and its phylogenetic significance". Zoological Journal of the Linnean Society. 140 (3): 335–351. doi: 10.1111/j.1096-3642.2003.00102.x . ISSN   0024-4082.
  19. ↑ Bordy, Emese M.; Sztanó, Orsolya; Rubidge, Bruce S.; Bumby, Adam (2011-03-01). "Early Triassic vertebrate burrows from the Katberg Formation of the south-western Karoo Basin, South Africa". Lethaia. 44 (1): 33–45. doi:10.1111/j.1502-3931.2010.00223.x. ISSN   1502-3931.
  20. ↑ Sérgio Dias-da-Silva, , Sean Patrick Modesto, and , Cesar Leandro Schultz (2006). "New material of Procolophon (Parareptilia: Procolophonoidea) from the Lower Triassic of Brazil, with remarks on the ages of the Sanga do Cabral and Buena Vista formations of South America". Canadian Journal of Earth Sciences. 43 (11): 1685–1693. doi:10.1139/e06-043.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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