Chunbo Yan

Lethally Hot Temperatures During the Early Triassic Greenhouse

Too-Hot Times Climate warming has been invoked as a factor contributing to widespread extinction events, acting as a trigger or amplifier for more proximal causes, such as marine anoxia. Sun et al. (p. 366; see the Perspective by Bottjer) present evidence that exceptionally high temperatures themselves may have caused some extinctions during the end-Permian. A rapid temperature rise coincided with a general absence of ichthyofauna in equatorial regions, as well as an absence of many species of marine mammals and calcareous algae, consistent with thermal influences on the marine low latitudes. Sea surface temperatures approached 40°C, which suggests that land temperatures likely fluctuated to even higher values that suppressed terrestrial equatorial plant and animal abundance during most of the Early Triassic. Global warming in the Early Triassic was so severe that equatorial latitudes were uninhabitable for many plants and animals. Global warming is widely regarded to have played a contributing role in numerous past biotic crises. Here, we show that the end-Permian mass extinction coincided with a rapid temperature rise to exceptionally high values in the Early Triassic that were inimical to life in equatorial latitudes and suppressed ecosystem recovery. This was manifested in the loss of calcareous algae, the near-absence of fish in equatorial Tethys, and the dominance of small taxa of invertebrates during the thermal maxima. High temperatures drove most Early Triassic plants and animals out of equatorial terrestrial ecosystems and probably were a major cause of the end-Smithian crisis.

Recovery tempo and pattern of marine ecosystems after the end-Permian mass extinction

High-resolution sampling of more than 10,000 microfossils from seven Late Permian−Middle Triassic paleoequatorial sections in south China refutes claims for a 5 m.y. recovery delay after the end-Permian mass extinction. We show that level-bottom seafloor diversity began to recover in the early Smithian, little more than 1 m.y. after the mass extinction, while recovery of reef-building metazoans began 4 m.y. later, in the Anisian. A further mass extinction in the late Smithian, identified in the pelagic fossil record, is weakly manifest as a temporary pause in diversification among benthic communities. In the Early Triassic of south China, the offshore diversity increase began before then, in shallower settings. The recovery from the end-Permian mass extinction in south China was therefore significantly more rapid and environmentally more complex than hitherto known.

Permian-Triassic conodonts from Dajiang (Guizhou, South China) and their implication for the age of microbialite deposition in the aftermath of the End-Permian mass extinction

The widespread microbialites deposition that followed the End-Permian mass extinction in the Tethyan realm have been intensively studied because of the evidence they provide on the nature of this crisis and its aftermath. However, the age of the microbialite event remains controversial. New conodont collection across the Permian-Triassic (P-T) transition from Dajiang (Guizhou Province, South China) in this study enable us to discriminate four conodont zones, in ascending order, they are: Hindeodus parvus zone, Isarcicella lobata zone, Isarcicella isarcica zone and Hindeodus sosioensis zone. The age of microbialite in the P-T transition at the Dajiang Section is considered to be within the Hindeodus parvus zone and thus to clearly post-date the main extinction crisis. Reviewing the age of onset of microbialites throughout the Tethyan regions reveals two different ages: a Hindeodus changxingensis zone age is dominant in south-western and westernmost Tethys, whilst most other regions show microbialite deposition began in the Hindeodus parvus zone. Our investigation also indicates that two conodont changes occur at this time: an increase of hindeodid species immediately following a sequence boundary and the mass extinction, and a phase of extinction losses in the earliest Triassic Isarcicella isarcica zone during highstand development.

UPPERMOST PERMIAN TO LOWER TRIASSIC CONODONTS AT BIANYANG SECTION, GUIHZOU PROVINCE, SOUTH CHINA

ABSTRACT A new conodont biostratigraphic study is presented from a key section on the flanks of the Permian-Triassic Great Bank of Guizhou, an isolated carbonate platform from South China, that has recently provided much key data for understanding the nature of this mass extinction interval. Detailed investigation at Bianyang (Guizhou Province) has revealed ten conodont zones, in ascending order: Clarkina yini Zone; Hindeodus changxingensis Zone; Hindeodus parvus Zone; Sweetospathodus kummeli Zone; Neospathodus dieneri Zone; Neospathodus cristagalli Zone; Discretella discreta Zone; Pachycladina-Parachirognathus assemblage zone; Icriospathodus collinsoni Zone; Triassospathodus homeri Zone. This allowed the Permian-Triassic boundary (PTB) to be defined in the section based on the first occurrence of Hindeodus parvus. Furthermore, it is proposed that the first occurrence of Discretella discreta can be used as an auxiliary reference for defining the Induan-Olenekian boundary when Novispathodus waageni is absent both at Bianyang and elsewhere.

Size variation of conodonts during the Smithian-Spathian (Early Triassic) global warming event

The Early Triassic Smithian–Spathian Boundary (SSB) crisis coincided with an episode of extreme warmth. A high-resolution stratigraphic framework comprising six conodont zones is provided in the Jiarong section, Nanpanjiang Basin, in South China. Detailed size measurements of 441 conodont elements of the closely related genera Neospathodus, Triassospathodus, and Novispathodus show for the first time that this clade suffered a temporary, but significant, size reduction during the SSB crisis. The size reduction of conodonts was probably caused by an episode of global warming.

The Relationship between the ＂Green-Bean Rock＂ Layers and Conodont Chiosella timorensis and Implications on Defining the Early-Middle Triassic Boundary in the Nanpanjiang Basin, South China

The Triassic “Green-bean Rock” (GBR) layers were widely recognized around the Early-Middle Triassic boundary interval in the Nanpanjiang Basin, South China. To determine the precise relationship between the GBR layers and the first appearance datum (FAD) of the conodont Chiosella timorensis, four Lower-Middle Triassic sections from the Nanpanjiang Basin, including the Gaimao, Bianyang II, Zuodeng and Wantou sections have been studied in detail. Detailed conodont biostratigraphy convinces us that there is no exact temporal relationship between the GBR layers and first occurrence of Ch. timorensis. Moreover, the numbers of the GBR layers are different from the place to place within the Nanpanjiang Basin, and the time span of the GBR layers was much longer than previously estimated. Global correlations show that the FAD of Ch. timorensis is contemporaneous basinwide and worldwide and more suitable marker defining the Olenekian-Anisian boundary (Early-Middle Triassic boundary) than any other proxies.

Response to Comment on "Lethally Hot Temperatures During the Early Triassic Greenhouse"

Goudemand et al. replot a subset of our well-constrained data using a new Early Triassic biostratigraphic scheme based on a lower-resolution ammonoid zonation scheme and hypothetical ammonoid-conodont correlation to produce a less distinct seawater temperature history. We dispute their unsubstantiated correlation and, consequently, their allegations.