Romano, Carlo; Goudemand, Nicolas; Vennemann, Torsten W; Ware, David; Schneebeli-Hermann, Elke; Hochuli, Peter A; Brühwiler, Thomas; Brinkmann, Winand; Bucher, Hugo (2013): Oxygen isotope values from biogenic apatite (conodont elements and fish teeth) from the Lower Triassic Mianwali Formation (Salt Range, Pakistan) [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.797718, Supplement to: Romano, C et al. (2013): Climate and biotic upheavals following the end-Permian mass extinction. Nature Geoscience, 6, 57-60, https://doi.org/10.1038/ngeo1667
Always quote citation above when using data! You can download the citation in several formats below.
Abstract:
Recovery from the end-Permian mass extinction is frequently described as delayed, with complex ecological communities typically not found in the fossil record until the Middle Triassic epoch. However, the taxonomic diversity of a number of marine groups, ranging from ammonoids to benthic foraminifera, peaked rapidly in the Early Triassic. These variations in biodiversity occur amidst pronounced excursions in the carbon isotope record, which are compatible with episodes of massive CO2 outgassing from the Siberian Large Igneous Province. Here we present a high-resolution Early Triassic temperature record based on the oxygen isotope composition of pristine apatite from fossil conodonts. Our reconstruction shows that the beginning of the Smithian substage of the Early Triassic was marked by a cooler climate, followed by an interval of warmth lasting until the Spathian substage boundary. Cooler conditions resumed in the Spathian. We find the greatest increases in taxonomic diversity during the cooler phases of the early Smithian and early Spathian. In contrast, a period of extreme warmth in the middle and late Smithian was associated with floral ecological change and high faunal taxonomic turnover in the ocean. We suggest that climate upheaval and carbon-cycle perturbations due to volcanic outgassing were important drivers of Early Triassic biotic recovery.
Coverage:
Latitude: 32.657222 * Longitude: 71.795278
Event(s):
Comment:
A print version of the table is available in pdf-format (A3) at "Other version:", the original excel-file as provided by the author is linked at hdl:10013/epic.40210.d002.
Parameter(s):
# | Name | Short Name | Unit | Principal Investigator | Method/Device | Comment |
---|---|---|---|---|---|---|
1 | Geologic age name | Geol age | Romano, Carlo | |||
2 | Lithologic unit/sequence | Unit | Romano, Carlo | |||
3 | Ammonoid zone | Ammonoid zone | Romano, Carlo | |||
4 | Bed | Bed | Romano, Carlo | |||
5 | Species | Species | Romano, Carlo | measured conodont species | ||
6 | δ18O, conodonts | δ18O conod | ‰ VSMOW | Romano, Carlo | Calculated average/mean values | |
7 | Sigma | Sigma | Romano, Carlo | d18O conodonts | ||
8 | δ18O, fish teeth | δ18O fish t | ‰ VSMOW | Romano, Carlo | Calculated average/mean values | |
9 | Sigma | Sigma | Romano, Carlo | d18O whole fish teeth | ||
10 | Phase | Phase | Romano, Carlo | delta18O phase |
License:
Creative Commons Attribution 3.0 Unported (CC-BY-3.0)
Size:
381 data points
Data
1 Geol age | 2 Unit | 3 Ammonoid zone | 4 Bed | 5 Species (measured conodont species) | 6 δ18O conod [‰ VSMOW] | 7 Sigma (d18O conodonts) | 8 δ18O fish t [‰ VSMOW] | 9 Sigma (d18O whole fish teeth) | 10 Phase (delta18O phase) |
---|---|---|---|---|---|---|---|---|---|
Spathian | "Niveaux intermédiaires" | Nam103 | Columbitella sp. | 18.7 | 18.6 | 0.5 | II | ||
Spathian | "Niveaux intermédiaires" | Nam710 | Columbitella sp. + Triassospathodus homeri | 18.2 | 0.7 | 20.1 | 0.3 | II | |
Spathian | "Niveaux intermédiaires" | Nam709 | ? | 18.9 | 0.4 | II | |||
Spathian | Bivalve Beds | BV9 | Borinella sp. | 17.3 | 18.6 | 0.9 | II | ||
Spathian | Bivalve Beds | BV8 | Columbitella sp. | 17.8 | 1.1 | II | |||
Spathian | Bivalve Beds | Nam707 | ? | 18.4 | 0.1 | II | |||
Spathian | Bivalve Beds | BV6 | Columbitella sp. + Triassospathodus homeri | 17.8 | 0.6 | 19.1 | 0.3 | II | |
Spathian | Bivalve Beds | BV5 | Columbitella sp. + Triassospathodus homeri | 16.8 | 0.2 | 16.3 | 0.4 | II | |
Spathian | Bivalve Beds | BV4 | Columbitella sp. | 17.3 | 0.9 | 19.5 | 0.2 | II | |
Spathian | Bivalve Beds | BV3 | - | 18.2 | 0.4 | II | |||
Spathian | Bivalve Beds | BV2 | Borinella sp + Columbitella sp. | 17.9 | 0.1 | II | |||
Spathian | Bivalve Beds | BV1 | Borinella sp. | 18.2 | 0.3 | II | |||
Smithian, late | Upper Ceratite Limestone | Glyptophiceras sinnatum | Nam32 | 16.7 | 0.0 | Id | |||
Smithian, late | Upper Ceratite Limestone | Glyptophiceras sinnatum | Nam42 | Novispathodus pingdingshanensis | 15.5 | Id | |||
Smithian, late | Upper Ceratite Limestone | Wasatchites distractus | - | - | Id | ||||
Smithian, middle | Upper Ceratite Limestone | Nyalamites angustecostatus | Nam68 | Novispathodus waageni | 16.3 | 0.2 | Id | ||
Smithian, middle | Upper Ceratite Limestone | Pseudoceltites multiplicatus | - | - | Id | ||||
Smithian, middle | Upper Ceratite Limestone | Nammalites pilatoides | Nam28 | Neospathodus spitiensis | 16.6 | 0.4 | Id | ||
Smithian, middle | Upper Ceratite Limestone | Brayardites compressus | Nam15 | Neospathodus spitiensis | 15.7 | 0.3 | Id | ||
Smithian, early | Upper Ceratite Limestone | Nam12 | Neospathodus spitiensis + Novispathodus waageni + Novispathodus pakistanensis | 16.3 | 0.0 | Id | |||
Smithian, early | Ceratite Sandstone | Euflemingites cirratus | Nam35 | Novispathodus waageni + Novispathodus pakistanensis | 16.6 | 0.3 | Id | ||
Smithian, early | Ceratite Sandstone | Clypeoceras superbum | Nam2 | Novispathodus waageni + Novispathodus pakistanensis | 17.3 | Ic | |||
Smithian, early | Ceratite Sandstone | Nam33 | Novispathodus pakistanensis | 17.8 | 0.2 | Ic | |||
Smithian, early | Ceratite Marls | Flemingites nanus | - | - | Ic | ||||
Smithian, early | Ceratite Marls | Xenodiscoides perplicatus | Nam65 | Novispathodus waageni + Novispathodus pakistanensis | 17.4 | 0.4 | 18.7 | 1.2 | Ic |
Smithian, early | Ceratite Marls | Xenodiscoides perplicatus | Nam532 | Novispathodus waageni + Novispathodus pakistanensis | 17.8 | 0.3 | 20.3 | 0.0 | Ic |
Smithian, early | Ceratite Marls | Nam726 | Novispathodus waageni | 17.3 | 0.2 | Ic | |||
Smithian, early | Ceratite Marls | Nam542 | Neospathodus cristagalli | 17.1 | 0.4 | Ic | |||
Smithian, early | Ceratite Marls | Flemingites bhargavai | Nam543 | Neospathodus cristagalli + Neospathodus dieneri + Novispathodus waageni | 16.6 | 0.6 | Ib | ||
Dienerian | Ceratite Marls | MH-D11 | Nam544 | Neospathodus cristagalli | 17.0 | 0.2 | Ib | ||
Dienerian | Ceratite Marls | MH-D10 | Nam63 | Neospathodus cristagalli | 17.1 | 0.2 | Ib | ||
Dienerian | Ceratite Marls | MH-D9 | Nam61 | Neospathodus cristagalli + Neospathodus dieneri | 17.4 | 0.3 | Ib | ||
Dienerian | Ceratite Marls | MH-D9 | Nam502 | Neospathodus cristagalli | 16.6 | 0.3 | Ib | ||
Dienerian | Ceratite Marls | MH-D8 | - | - | Ib | ||||
Dienerian | Ceratite Marls | MH-D7 | Nam100 | - | 13.5 | Ib | |||
Dienerian | Ceratite Marls | MH-D6 | Nam53 | Neospathodus cristagalli + Neospathodus dieneri | 16.1 | 0.2 | Ib | ||
Dienerian | Ceratite Marls | MH-D5 | Nam50 | Neospathodus cristagalli | 16.5 | 0.4 | 14.2 | 0.2 | Ib |
Dienerian | Ceratite Marls | MH-D5 | Nam526 | Neospathodus dieneri group | 16.2 | 14.8 | 0.1 | Ib | |
Dienerian | Ceratite Marls | Nam526 | Neospathodus dieneri group | 16.9 | 0.5 | Ib | |||
Dienerian | Ceratite Marls | MH-D4 | Nam384 | Neospathodus dieneri group | 16.5 | 0.4 | Ib | ||
Dienerian | Ceratite Marls | MH-D3 | - | - | Ib | ||||
Dienerian | Lower Ceratite Limestone | MH-D2 | LCL-C2 | Neogondolella spp. | 16.2 | Ib | |||
Dienerian | Lower Ceratite Limestone | MH-D1 | Nam332 | Sweetospathodus kummeli | 17.1 | 0.2 | 14.1 | 0.4 | Ia |
Dienerian | Lower Ceratite Limestone | Nam330 | Sweetospathodus kummeli | 17.9 | Ia | ||||
Dienerian | Lower Ceratite Limestone | Nam330 | Sweetospathodus kummeli | 16.9 | 0.3 | Ia | |||
Griesbachian | Lower Ceratite Limestone | MH-G3 | LCL-C1 | Neogondolella spp. | 20.5 | 18.7 | 0.1 | Ia | |
Griesbachian | Kathwai Member | MH-G2 | Nam376 | Neogondolella spp. | 16.9 | 0.8 | 15.7 | Ia | |
Griesbachian | Kathwai Member | Nam326 | Neogondolella spp. | 16.4 | 14.0 | 0.9 | Ia | ||
Griesbachian | Kathwai Member | Nam326 | Neogondolella spp. | 17.4 | 0.2 | ||||
Griesbachian | Kathwai Member | MH-G1 | - | - |