| 1. |
- Agić, Heda, 1989-
(författare)
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Palaeobiology and diversification of Proterozoic-Cambrian photosynthetic eukaryotes
- 2015
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- One of the most important events in the history of life is the evolution of the complex, eukaryotic cell. The eukaryotes are complex organisms with membrane-bound intracellular structures, and they include a variety of both single-celled and multicellular organisms: plants, animals, fungi and various protists. The evolutionary origin of this group may be studied by direct evidence of past life: fossils. The oldest traces of eukaryotes have appeared by 2.4 billion years ago (Ga), and have additionally diversified in the period around 1.8 Ga. The Mesoproterozoic Era (1.6-1 Ga) is characterised by the first evidence of the appearance complex unicellular microfossils, as well as innovative morphologies, and the evolution of sexual reproduction and multicellularity. For a better understanding of the early eukaryotic evolution and diversification patterns, a part of this thesis has focused on the microfossil records from various time periods and geographic locations. Examination of microfossil morphology, cell wall microstructure and biochemical properties, reflect their intracellular complexity and function, and allow reconstructions of their life cycle, as well as observing the evolutionary pattern of change from Mesoproterozoic, to Cambrian-Ordovician transition. Several case studies included assemblages deriving from Mesoproterozoic, Neoproterozoic and early Paleozoic time intervals that show disparate morphotypes and innovative features indicative of algal clades. The Mesoproterozoic Ruyang Group in northern China has yielded a diverse microfossil assemblage that provides important clues about the diversification of different eukaryotic groups. Furthermore these microfossils contributed an additional evidence for the emergence of the crown group Eukarya by 1.7-1.4 Ga. In another part of this thesis, examination of wall microstructure and chemical properties via Raman spectroscopy has been used to assess the biological affinities of various Neoproterozoic problematic carbonaceous compression fossils. Studies on the early Phanerozoic (c. 545-485 Ma) assemblages from Estonia reconstructed patterns of the early radiations of phytoplankton and its evolutionary innovations. A continuing theme in this thesis has been using a combination of evidence of microfossils’ fine-scale morphology, ecology and chemical properties to determine their function in life, in addition to their systematic position.
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| 2. |
- Babcock, Loren, et al.
(författare)
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Proposed reassessment of the Cambrian GSSP
- 2014
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Ingår i: Journal of African Earth Sciences. - : Elsevier BV. - 1464-343X. ; 98, s. 3-10
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Tidskriftsartikel (refereegranskat)abstract
- Since the time of its ratification in 1992, the Cambrian GSSP, 23 m above the base of Member 2A (Quaco Road Member) of the Chapel Island Formation, Fortune Head section, Newfoundland, Canada, has been challenged as posing an ambiguous correlation level. Difficulties have been encountered in precisely correlating the horizon coinciding with the GSSP to strata on most paleocontinents, but especially to Siberia and South China (Gondwana). The GSSP point, which was intended to coincide with the base of the Treptichnus pedum (formerly Phycodes pedum or Trichophycus pedum) Ichnozone at the FAD of the trace fossil T. pedum, occurs above the first appearance of the trace in the stratotype section. Trace fossils of other forms in the stratotype provide a means of bracketing the position of the GSSP, but are imprecise guides for correlation globally. Other chronostratigraphic guides are unavailable at the stratotype because of a dominance of coarse siliciclastic lithologies and metamorphic overprint. To facilitate global correlation of the Cambrian base and ensure nomenclatural stability to the extent possible, discussion of the merits and perceived weaknesses of the Cambrian GSSP is sought. Possible solutions to the problems surrounding the current GSSP definition are addressed in hopes that the global scientific community will actively participate in developing a well-reasoned, practical solution that will stand the test of time. (C) 2014 Elsevier Ltd. All rights reserved.
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| 3. |
- Hoshino, Yosuke, et al.
(författare)
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Cryogenian evolution of stigmasteroid biosynthesis
- 2017
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Ingår i: Science Advances. - : AMER ASSOC ADVANCEMENT SCIENCE. - 2375-2548. ; 3:9
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Tidskriftsartikel (refereegranskat)abstract
- Sedimentary hydrocarbon remnants of eukaryotic C-26-C-30 sterols can be used to reconstruct early algal evolution. Enhanced C-29 sterol abundances provide algal cellmembranes a density advantage in large temperature fluctuations. Here, we combined a literature review with new analyses to generate a comprehensive inventory of unambiguously syngenetic steranes in Neoproterozoic rocks. Our results show that the capacity for C-29 24ethyl- sterol biosynthesis emerged in the Cryogenian, that is, between 720 and 635 million years ago during the Neoproterozoic Snowball Earth glaciations, which were an evolutionary stimulant, not a bottleneck. This biochemical innovation heralded the rise of green algae to global dominance of marine ecosystems and highlights the environmental drivers for the evolution of sterol biosynthesis. The Cryogenian emergence of C-29 sterol biosynthesis places benchmark for verifying older sterane signatures and sets a new framework for our understanding of early algal evolution.
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| 4. |
- LoDuca, Steven T., et al.
(författare)
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Reexamination of Yuknessia from the Cambrian of China and first report of Fuxianospira from North America
- 2015
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Ingår i: Journal of Paleontology. - : Cambridge University Press (CUP). - 0022-3360 .- 1937-2337. ; 89:6, s. 899-911
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Tidskriftsartikel (refereegranskat)abstract
- Yuknessia Walcott, 1919 recently was transferred from the green algae to the Phylum Hemichordata on the basis of new details observed for the type species, Y. simplex, from the Burgess Shale Formation (Cambrian Stage 5) of British Columbia. This has prompted reexamination of material attributed to Yuknessia from various Cambrian localities in South China. Findings preclude both a Yuknessia and a hemichordate affinity for all of the Chinese study material, and most of this material is formally transferred to Fuxianospira Chen and Zhou, 1997, a taxon common in the Chengjiang biota. Comparable material from the Cambrian Marjum, Wheeler, and Burgess Shale formations of North America is also assigned to Fuxianospira, and this reassignment expands both the paleogeographic and stratigraphic range of this taxon. All aspects of the study specimens, including details obtained from scanning electron microscopy, are consistent with an algal affinity, as proposed in the original descriptions of the Chinese material.
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| 5. |
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| 6. |
- Qu, Yuangao, et al.
(författare)
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Carbonaceous biosignatures of diverse chemotrophic microbial communities from chert nodules of the Ediacaran Doushantuo Formation
- 2017
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Ingår i: Precambrian Research. - : Elsevier BV. - 0301-9268 .- 1872-7433. ; 290, s. 184-196
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Tidskriftsartikel (refereegranskat)abstract
- The Ediacaran Doushantuo Formation (DST) is renowned for exceptionally preserved Precambrian fossils including metazoans. Some of these fossils, particularly microfossils such as multicellular algae and acanthomorphic acritarchs, are preserved in DST chert nodules. To better understand the geomicrobiological processes that contributed to the authigenic formation of DST chert nodules and facilitated exceptional fossil preservation, we analyzed organic matter in these chert nodules and the surrounding matrix (calcareous mudstone) using multiple in-situ techniques: confocal laser Raman spectroscopy, micro-Fourier transform infrared spectroscopy (FTIR), and secondary ion mass spectroscopy (SIMS). We found strong ultrastructural, chemical, and isotopic heterogeneities in the organic matter as indicated by the Raman spectral parameter I-1350/1600 ranging from 0.49 to 0.88, the infrared spectral index R3/2 from 0.12 to 0.90, and an estimated δ13Corg-SIMS range of 44‰ (V-PDB). These micron-scale heterogeneities imply that the organic matter preserved in the DST chert nodules is derived from different carbonaceous sources in a diverse microbial ecosystem, including eukaryotic and/or prokaryotic photoautotrophs, as well as chemotrophs involved in the fermentation and probably anaerobic oxidation of organic remains. Thus, the microbial ecosystems in Ediacaran ocean waters and sediments were more complex than previously thought, and these microbial processes controlled dynamic micro-environments in DST sediments where chert nodules were formed and fossils were mineralized. The results also show that variations in the relative abundances, activities, and interactions of co-existing microorganisms in DST sediments may have modulated δ13Corg shifts, causing local decoupling between δ13Corg and δ13Ccarb as measured in bulk samples.
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| 7. |
- Willman, Sebastian, Docent
(författare)
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The Ediacaran Diversification of Organic-walled Microbiota : Ocean Life 600 Million Years Ago
- 2008
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The only direct evidence of past life is provided by fossils. Fossils tell us about the evolution of life on Earth and they give us clues concerning ancient environments. The Ediacaran Period (roughly 635-542 million years ago) is characterised by the appearance and diversification of various microbiota and also the diversification of metazoans. Well-preserved organic-walled microfossils referred to as acritarchs occur abundantly in Ediacaran sedimentary successions in the Officer Basin in South Australia. Acritarch assemblages from the Giles 1 and Murnaroo 1 drillcores show a wide morphological disparity and are taxonomically diverse. Assemblages change over short stratigraphic intervals which enables the recognition of different biozones. The presence of taxa common between Australia, Siberia, Baltica and China provides a means for global correlation of the Ediacaran System. Examination of the wall ultrastructure of several acritarch specimens by use of transmission electron microscopy reveals a complexity in the cell wall that is not seen in prokaryotes but is indicative in some cases of particular clades of microalgae. Wall ultrastructures range from single-layered to three- and four-layered and from homogeneous to porous. The wall ultrastructure can be used to assess biological affinities and the affinities of the studied taxa in relation to green algae, dinoflagellates and metazoans are discussed. However, before taxonomic interpretations can be made with confidence, an understanding of taphonomic degradation of microorganisms is required. With focus on illustrated specimens, one part of this thesis explains what happens to an acritarch as it undergoes various types of degradation and why an understanding of these processes is important for taxonomic identification. A meteorite impact in South Australia spread an ejecta layer over a 550 km radius area. This ejecta layer is recognised in subsurface drillcores and provides an independent stratigraphic marker horizon that supports an acritarch-based correlation.
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| 8. |
- Xiao, Shuhai, et al.
(författare)
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Towards an Ediacaran Time Scale : Problems, Protocols, and Prospects
- 2016
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Ingår i: Episodes. - : International Union of Geological Sciences. - 0705-3797 .- 2586-1298. ; 39:4, s. 540-555
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Tidskriftsartikel (refereegranskat)abstract
- The Ediacaran Period follows the Cryogenian Period in the wake of a snowball Earth glaciation and precedes the Cambrian Period with its rising tide of animal radiation. It is also the longest among all stratigraphically defined geological periods, lasting 94 million years (635-541 Ma). Hence, a good Ediacaran time scale is essential, not only to elucidate geological time, but also to provide a temporal context for extreme climatic events and transformative evolutionary transitions. Ediacaran fossils are known from many sections and boreholes around the world, permitting ready age recognition and stratigraphic correlation of Ediacaran strata. However, the Ediacaran fossil record is colored by taphonomic biases that variously affect the preservation of the soft-bodied organisms that dominated Ediacaran marine ecosystems, and the Phanerozoic approach of defining stratigraphic boundaries using the first appearance datum (FAD) of widely distributed, rapidly evolving, easily recognizable, and readily preservable species would have limited success in the Ediacaran System. The subdivision of the Ediacaran System must therefore be founded on a holistic approach integrating biostratigraphic, chemostratigraphic, and geochronometric data for correlation. Series-level subdivision of the Ediacaran System is a challenging task, and alternative models subdividing the Ediacaran System into two or three series can be recognized. Resolving these alternatives critically depends on obtaining further data to constrain the age, duration, and global extent of the Shuram negative delta C-13 excursion, to calibrate and correlate Ediacaran acanthomorph biozones, and to determine the temporal relationship among the Shuram excursion, the Gaskiers glaciation, and Ediacaran acanthomorph biozones. Stage-level subdivisions at the bottom and top of the Ediacaran System, however, are realistic goals in the near future, and we propose that the subdivision of the Ediacaran System should initially aim at the second Ediacaran stage (SES) and the terminal Ediacaran stage (TES) where stratigraphic information is relatively rich and consensus for stratigraphic correlation is emerging. Potential stratigraphic markers for the definition of the SES include the post-glacial radiation of eukaryotes as represented by the first appearance of acanthomorph acritarchs, the termination of the cap carbonate series, or the end of the negative delta C-13 excursion (EN1 = Ediacaran negative excursion 1) associated with the cap carbonate. Terminal Ediacaran strata are well dated and host several taxa of skeletal and tubular fossils that postdate the Shuram negative delta C-13 excursion (or its probable equivalent, EN3 = Ediacaran negative excursion 3) where their stratigraphic relationship can be determined; these biostratigraphic markers may be used to define the TES in a Phanerozoic fashion. Additional Ediacaran stages between the SES and TES can be envisioned. Through collaborative efforts in the Ediacaran community, we hope that the first Precambrian stage will be established in the near future to facilitate a better understanding of the geological aftermath of snowball Earth, the redox history of global oceans, the early evolution of multicellular life, and the evolutionary fuse of the Cambrian explosion.
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| 9. |
- Zhang, Huaqiao, et al.
(författare)
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Musculature of an Early Cambrian cycloneuralian animal
- 2023
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Ingår i: Proceedings of the Royal Society B: Biological Sciences. - 0962-8452. ; 290:2008
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Tidskriftsartikel (refereegranskat)abstract
- Cycloneuralians are ecdysozoans with a fossil record extending to the Early Cambrian Fortunian Age and represented mostly by cuticular integuments. However, internal anatomies of Fortunian cycloneuralians are virtually unknown, hampering our understanding of their functional morphology and phylogenetic relationships. Here we report the exceptional preservation of cycloneuralian introvert musculature in Fortunian rocks of South China. The musculature consists of an introvert body-wall muscular grid of four circular and 36 radially arranged longitudinal muscle bundles, as well as an introvert circular muscle associated with 19 roughly radially arranged, short retractors. Collectively, these features support at least a scalidophoran affinity, and the absence of muscles associated with a mouth cone and scalids further indicates a priapulan affinity. As in modern scalidophorans, the fossil musculature, and particularly the introvert circular muscle retractors, may have controlled introvert inversion and facilitated locomotion and feeding. This work supports the evolution of scalidophoran-like or priapulan-like introvert musculature in cycloneuralians at the beginning of the Cambrian Period.
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