Chuanming Zhou

Pulsed oxidation and biological evolution in the Ediacaran Doushantuo Formation

Recent geochemical data from Oman, Newfoundland, and the western United States suggest that long-term oxidation of Ediacaran oceans resulted in progressive depletion of a large dissolved organic carbon (DOC) reservoir and potentially triggered the radiation of acanthomorphic acritarchs, algae, macroscopic Ediacara organisms, and, subsequently, motile bilaterian animals. However, the hypothesized coupling between ocean oxidation and evolution is contingent on the reliability of continuous geochemical and paleontological data in individual sections and of intercontinental correlations. Here we report high-resolution geochemical data from the fossil-rich Doushantuo Formation (635–551 Ma) in South China that confirm trends from other broadly equivalent sections and highlight key features that have not been observed in most sections or have received little attention. First, samples from the lower Doushantuo Formation are characterized by remarkably stable δ13Corg (carbon isotope composition of organic carbon) values but variable δ34SCAS (sulfur isotope composition of carbonate-associated sulfate) values, which are consistent with a large isotopically buffered DOC reservoir and relatively low sulfate concentrations. Second, there are three profound negative δ13Ccarb (carbon isotope composition of carbonate) excursions in the Ediacaran Period. The negative δ13Ccarb excursions in the middle and upper Doushantuo Formation record pulsed oxidation of the deep oceanic DOC reservoir. The oxidation events appear to be coupled with eukaryote diversity in the Doushantuo basin. Comparison with other early Ediacaran basins suggests spatial heterogeneity of eukaryote distribution and redox conditions. We hypothesize that the distribution of early Ediacaran eukaryotes likely tracked redox conditions and that only after ≈551 Ma (when Ediacaran oceans were pervasively oxidized) did evolution of oxygen-requiring taxa reach global distribution.

New constraints on the ages of Neoproterozoic glaciations in south China

The most complete Neoproterozoic successions in south China contain three diamictite intervals in the Changan, Tiesiao, and Nantuo Formations. The youngest and most widespread Nantuo glacial deposit overlies the Datangpo Formation and underlies the fossil- rich Doushantuo Formation. Previous authors have correlated the Nantuo diamictite to either Sturtian or Marinoan glacial deposits elsewhere. Here we report sedimentary and δ13C chemostratigraphic data of the Doushantuo cap dolostone, which overlies the Nantuo Formation. Facies-dependent variation in δ13C is interpreted as evidence for spatial heterogeneity in δ13C and/or temporal diachroneity in the initiation of cap carbonate sedimentation. Sedimentary and chemostratigraphic data are indicative of a Marinoan age for the Nantuo glaciation. This inference is supported by a new U-Pb zircon age of 663 ± 4 Ma from a tuffaceous bed in the Datangpo Formation. The new date and other isotopic ages from south China constrain the age of the Changan and Tiesiao glaciation(s) as between 761 ± 8 Ma and 663 ± 4 Ma, and the Nantuo glaciation as between 663 ± 4 Ma and 599 ± 4 Ma.

An early Ediacaran assemblage of macroscopic and morphologically differentiated eukaryotes

The deep-water Avalon biota (about 579 to 565 million years old) is often regarded as the earliest-known fossil assemblage with macroscopic and morphologically complex life forms. It has been proposed that the rise of the Avalon biota was triggered by the oxygenation of mid-Ediacaran deep oceans. Here we report a diverse assemblage of morphologically differentiated benthic macrofossils that were preserved largely in situ as carbonaceous compressions in black shales of the Ediacaran Lantian Formation (southern Anhui Province, South China). The Lantian biota, probably older than and taxonomically distinct from the Avalon biota, suggests that morphological diversification of macroscopic eukaryotes may have occurred in the early Ediacaran Period, perhaps shortly after the Marinoan glaciation, and that the redox history of Ediacaran oceans was more complex than previously thought.

Triple oxygen isotope evidence for elevated CO2 levels after a Neoproterozoic glaciation

Understanding the composition of the atmosphere over geological time is critical to understanding the history of the Earth system, as the atmosphere is closely linked to the lithosphere, hydrosphere and biosphere. Although much of the history of the lithosphere and hydrosphere is contained in rock and mineral records, corresponding information about the atmosphere is scarce and elusive owing to the lack of direct records. Geologists have used sedimentary minerals, fossils and geochemical models to place constraints on the concentrations of carbon dioxide, oxygen or methane in the past. Here we show that the triple oxygen isotope composition of sulphate from ancient evaporites and barites shows variable negative oxygen-17 isotope anomalies over the past 750 million years. We propose that these anomalies track those of atmospheric oxygen and in turn reflect the partial pressure of carbon dioxide () in the past through a photochemical reaction network linking stratospheric ozone to carbon dioxide and to oxygen. Our results suggest that was much higher in the early Cambrian than in younger eras, agreeing with previous modelling results. We also find that the 17O isotope anomalies of barites from Marinoan (∼635 million years ago) cap carbonates display a distinct negative spike (around -0.70‰), suggesting that by the time barite was precipitating in the immediate aftermath of a Neoproterozoic global glaciation, the was at its highest level in the past 750 million years. Our finding is consistent with the ‘snowball Earth’ hypothesis and/or a massive methane release after the Marinoan glaciation.

New Ediacara fossils preserved in marine limestone and their ecological implications.

Ediacara fossils are central to our understanding of animal evolution on the eve of the Cambrian explosion, because some of them likely represent stem-group marine animals. However, some of the iconic Ediacara fossils have also been interpreted as terrestrial lichens or microbial colonies. Our ability to test these hypotheses is limited by a taphonomic bias that most Ediacara fossils are preserved in sandstones and siltstones. Here we report several iconic Ediacara fossils and an annulated tubular fossil (reconstructed as an erect epibenthic organism with uniserial arranged modular units), from marine limestone of the 551–541 Ma Dengying Formation in South China. These fossils significantly expand the ecological ranges of several key Ediacara taxa and support that they are marine organisms rather than terrestrial lichens or microbial colonies. Their close association with abundant bilaterian burrows also indicates that they could tolerate and may have survived moderate levels of bioturbation.

Rare helical spheroidal fossils from the Doushantuo Lagerstatte: Ediacaran animal embryos come of age?

A small quantity of helically coiled spheroidal fossils has been recovered from acid digestion of phosphorite samples from the Ediacaran Doushantuo Formation, South China. These fossils consist of an internal body enclosed in a sculptured envelope that is very similar to that of Doushantuo animal eggs and blastula embryos such as Megasphaera ornata . A hallmark of these fossils is a three-dimensional spiral structure, which always consists of three clockwise coils, and occurs on both the envelope and the internal body. The spiral structure consists of a spiral tunnel or canal flanked by two raised levees, and it is punctured by a series of holes. Some specimens show evidence of uncoiling, invagination along the spiral structure, or bipectinate furrowing on the band between canals. A possible ontogenetic link between these helical spheroidal fossils and Megasphaera ornata is suggested by similar size, similar envelope sculptures, and co-occurrence. We tentatively interpret these fossils as postblastula embryos related to Megasphaera ornata . Thus, they may represent the most advanced embryonic fossils so far known from the Ediacaran, although their adult morphologies and phylogenetic affinity remain unknown.

Basal Cambrian Microfossils from the Yangtze Gorges Area (South China) and the Aksu Area (Tarim Block, Northwestern China)

Abstract The basal Cambrian marks the beginning of an important chapter in the history of life. However, most paleontological work on the basal Cambrian has been focused on skeletal animal fossils, and our knowledge about the primary producers—cyanobacteria and eukaryotic phytoplankton (e.g., acritarchs)—is limited. In this research, we have investigated basal Cambrian acritarchs, coccoidal microfossils, and cyanobacteria preserved in phosphorites and cherts of the Yanjiahe Formation in the Yangtze Gorges area (South China) and the Yurtus Formation in the Aksu area (Tarim Block, northwestern China). Our study confirms the occurrence in these two formations of small acanthomorphic acritarchs characteristic of the basal Cambrian Asteridium–Comasphaeridium–Heliosphaeridium (ACH) assemblage. These acritarchs include abundant Heliosphaeridium ampliatum (Wang, 1985) Yao et al., 2005, common Yurtusia uniformis n. gen. and n. sp., and rare Comasphaeridium annulare (Wang, 1985) Yao et al., 2005. In addition, these basal Cambrian successions also contain the clustered coccoidal microfossil Archaeophycus yunnanensis (Song in Luo et al., 1982) n. comb., several filamentous cyanobacteria [Cyanonema majus n. sp., Oscillatoriopsis longa Timofeev and Hermann, 1979, and Siphonophycus robustum (Schopf, 1968) Knoll et al., 1991], and the tabulate tubular microfossil Megathrix longus L. Yin, 1987a, n. emend. Some of these taxa (e.g., H. ampliatum, C. annulare, and M. longus) have a wide geographic distribution but occur exclusively in basal Cambrian successions, supporting their biostratigraphic importance. Comparison between the stratigraphic occurrences of microfossils reported here and skeletal animal fossils published by others suggests that animals and phytoplankton radiated in tandem during the Cambrian explosion.

PROBLEMATIC MACROFOSSILS FROM EDIACARAN SUCCESSIONS IN THE NORTH CHINA AND CHAIDAM BLOCKS: IMPLICATIONS FOR THEIR EVOLUTIONARY ROOTS AND BIOSTRATIGRAPHIC SIGNIFICANCE

Abstract Upper Neoproterozoic successions in the North China and nearby Chaidam blocks are poorly documented. North China successions typically consist of a diamictite unit overlain by siltstone, sandstone, or slate. Similar successions occur in Chaidam, although a cap carbonate lies atop the diamictite unit. The diamictites in both blocks have been variously interpreted as Cryogenian, Ediacaran, or Cambrian glacial deposits. In this paper, we describe problematic macrofossils collected from slate of the upper Zhengmuguan Formation in North China and sandstone of the Zhoujieshan Formation in Chaidam; both fossiliferous formations conformably overlie the aforementioned diamictites. Some of these fossils were previously interpreted as animal traces. Our study recognizes four genera and five species—Helanoichnus helanensis Yang in Yang and Zheng, 1985, Palaeopascichnus minimus n. sp., Palaeopascichnus meniscatus n. sp., Horodyskia moniliformis? Yochelson and Fedonkin, 2000, and Shaanxilithes cf. ningqiangensis Xing et al., 1984. None of these taxa can be interpreted as animal traces. Instead, they are problematic body fossils of unresolved phylogenetic affinities. The fundamental bodyplan similarity between Horodyskia and Palaeopascichnus, both with serially repeated elements, indicates a possible phylogenetic relationship. Thus, at least some Ediacaran organisms may have a deep root because Horodyskia also occurs in Mesoproterozoic successions. Among the four genera reported here, Palaeopascichnus Palij, 1976 and Shaanxilithes Xing et al., 1984 have been known elsewhere in upper Ediacaran successions, including the Dengying Formation (551–542 Ma) in South China. If these two genera have biostratigraphic significance, the fossiliferous units in North China and Chaidam may be upper Ediacaran as well. Thus, the underlying diamictites in North China and Chaidam cannot be of Cambrian age, although their correlation with Ediacaran and Cryogenian glaciations remains unclear. As no other Neoproterozoic diamictite intervals are known in North China and Chaidam, perhaps only one Neoproterozoic glaciation is recorded in that area.

Towering sponges in an Early Cambrian Lagerstätte: Disparity between nonbilaterian and bilaterian epifaunal tierers at the Neoproterozoic-Cambrian transition

Epifaunal, suspension-feeding bilaterian animals in the Cambrian lived close to the sediment-water interface, and hence their ecological tiering levels were low (<10 cm). Here we report an Early Cambrian (Diandongian or probably Tommotian-Atdabanian) Lagerstatte from the Hetang Formation in Anhui Province, south China. The Hetang biota is characterized by high-tiering (to 50 cm) sponges and small (<0.5 cm) bilaterians (including orthothecid hyoliths and bivalved arthropods). Nonbilaterian suspension feeders (sponges, cnidarians, and archaeocyathids) as high-tiering animals and bilaterian suspension feeders as low-tiering animals also characterize other Neoproterozoic-Cambrian assemblages, such as the Ediacaran, Chengjiang, Burgess Shale, and Sinsk biotas. These data are consistent with medium- to high-tiering levels in Neoproterozoic-Cambrian epifaunal communities, but suggest that nonbilaterians achieved such tiering levels long before bilaterian suspension feeders did so in the Early Ordovician. The disparity between bilaterian and nonbilaterian tierers during the Neoproterozoic-Cambrian transition and the delayed appearance of high-tiering bilaterians demand phylogenetic and ecological explanations. The Cambrian substrate revolution may have triggered a cascade of ecological evolution, including the rise of bilaterian animals in high-tiering levels during the Ordovician radiation of the Paleozoic fauna.

Ediacaran acanthomorphic acritarchs and other microfossils from chert nodules of the upper Doushantuo Formation in the Yangtze Gorges area, South China

Abstract Silicified microfossils preserved in chert nodules of the Doushantuo Formation in the Yangtze Gorges area of South China have great potential to improve the biostratigraphic subdivision and correlation of the Ediacaran System. This potential can be realized only if solid taxonomy is available. However, a systematic treatment of these microfossils (particularly acanthomorphic acritarchs) is lacking, greatly limiting their biostratigraphic potential. This paper presents the systematic paleontology of silicified microfossils from upper Doushantuo Formation (Member III) chert nodules at three sections in the Yangtze Gorges area. More than 90 species of microfossils are described, including 66 named taxa of acanthomorphs, seven named taxa of sphaeromorphs, 12 taxa of cyanobacterial filaments and coccoids, four taxa of algal thalli, and two species of tubular microfossils. Several acritarch species, including Appendisphaera clava n. sp., Mengeosphaera grandispina n. sp., M. stegosauriformis n. sp., Leiosphaeridia, and possibly Sinosphaera rupina, are shown to be multicellular organisms, consistent with the proposition that some Ediacaran acritarchs may be diapause eggs of early animals. This study supports the view that the Tianzhushania spinosa acanthomorph biozone is unique to the lower Doushantuo Formation in South China (and perhaps its equivalent in northern India) and that Ediacaran acanthomorph assemblages from Australia, Siberia, and East European Platform are younger than the Tianzhushania spinosa biozone. It is proposed that the first occurrence of Hocosphaeridium anozos, a species with easily recognizable morphology and wide taphonomic and geographic distributions, be used to define the second Doushantuo acanthomorph biozone succeeding the Tianzhushania spinosa biozone. New taxa described in this paper include three new genera (Bispinosphaera n. gen.; Yushengia n. gen.; and Granitunica n. gen.) and 40 new species: Appendisphaera? brevispina n. sp., A. clava n. sp., A.? hemisphaerica n. sp., A. longispina n. sp., A. setosa n. sp., Bispinosphaera peregrina n. gen. n. sp., Crinita paucispinosa n. sp., Ericiasphaera densispina n. sp., Hocosphaeridium dilatatum n. sp., Knollisphaeridium denticulatum n. sp., K. longilatum n. sp., K. obtusum n. sp., K. parvum n. sp., Mengeosphaera angusta n. sp., M. bellula n. sp., M. cf. bellula n. sp., M. constricta n. sp., M.? cuspidata n. sp., M.? gracilis n. sp., M. grandispina n. sp., M. latibasis n. sp., M. minima n. sp., M. spicata n. sp., M. spinula n. sp., M. stegosauriformis n. sp., M. triangularis n. sp., M. uniformis n. sp., Sinosphaera asteriformis n. sp., Tanarium acus n. sp., T. elegans n. sp., T. longitubulare n. sp., T.? minimum n. sp., T. obesum n. sp., T. varium n. sp., Urasphaera fungiformis n. sp., U. nupta n. sp., Yushengia ramispina n. gen. n. sp., Granitunica mcfaddeniae n. gen. n. sp., Osculosphaera arcelliformis n. sp., and O. membranifera n. sp.