Life through an Ediacaran glaciation: Shale- and diamictite-hosted organic-walled microfossil assemblages from the late Neoproterozoic of the Tanafjorden area, northern Norway

New organic-walled microfossil (OWM) assemblages are reported from upper Neoproterozoic glacial and interglacial siliciclastic deposits in Finnmark, northern Norway. A nearly continuous sedimentary succession of the Vestertana Group contains two glaciogenic units, the Smalfjorden and Mortensnes formations, interpreted as end-Cryogenian Marinoan and Ediacaran glaciations, respectively. We investigated the OWM record in the Nyborg, Mortensnes, and Stáhpogieddi formations to assess the impact of a glacial interval on the diversity of microscopic eukaryotes. A modified acid-extraction technique was applied to recover OWM from the diamictite matrix. The upper Nyborg Formation contains morphologically complex Doushantuo-Pertatataka acritarchs (DPA), restricting the age of the Nyborg Formation to early-mid Ediacaran. DPA occur below the dolostones that record a negative carbon isotope excursion correlated with the Shuram anomaly and below a glacial diamictite. A decline in species richness and compositional change is observed in the Mortensnes glacial assemblage. DPA are replaced by bacterial filaments and cell aggregates. The overlying Indreelva Member, Stáhpogieddi Formation contains Ediacara-type biota and palaeopascichnids, but only a depauperate OWM assemblage of leiosphaerids and flask-shaped microfossils characteristic of the late Ediacaran.The succession of assemblages in the Vestertana Group demonstrates a turnover from large eukaryotic OWM to a microbial community in the glacial interval, to a low diversity post-glacial assemblage during the rise of macroscopic life. We compared the Vestertana record to global DPA occurrences. Although one DPA assemblage zone postdates the Shuram excursion, no DPA occur above Ediacaran glacial diamictites in successions where those deposits are present. Considering this, and the community changes in the Vestertana succession, we suggest that DPA were affected by the onset of an Ediacaran glaciation. Lastly, we combined the biostratigraphic markers in the Vestertana Group to constrain the age of the Mortensnes diamictite

Rare earth elements and neodymium and strontium isotopic constraints on provenance switch and post-depositional alteration of fossiliferous Ediacaran and lowermost Cambrian strata from Arctic Norway.

The Digermulen Peninsula in northeastern Finnmark, Arctic Norway, comprises one of the most complete Ediacaran–Cambrian transitions worldwide with a nearly continuous record of micro- and macrofossils from the interval of the diversification of complex life. Here, we report on the provenance and post-depositional alteration of argillaceous mudstones from the Digermulen Peninsula using rare earth elements and Sm–Nd and Rb–Sr isotopic systematics to provide an environmental context and better understand this important transition in Earth’s history. The studied sections comprise a mid-Ediacaran glacial–interglacial cycle, including the Nyborg Formation (ca. 590 Ma) and Mortensnes Formation (related to the ca. 580 Ma-old Gaskiers glaciation), and the Stahpogieddi ´ Formation (ca. 560–537 Ma), which yields Ediacara-type fossils in the Indreelva Member and contains the Ediacaran–Cambrian boundary interval in the Manndrapselva Member and basal part of the informal Lower Breidvika member (ca. 537–530 Ma). Three sample groups, (1) Nyborg and Mortensnes formations, (2) the lowermost five samples from the Indreelva Member and (3) the remaining samples from the Indreelva as well as from the Manndrapselva and Lower Breidvika members, can be distinguished, belonging to distinct depositional units. All samples have negative εNd(T) values (− 6.00 to − 21.04) indicating a dominant input of terrigenous detritus with an old continental crust affinity. Significant shifts in Sm–Nd isotope values are related to changes in the sediment source, i.e. Svecofennian province vs Karelian province vs Svecofennian province plus in addition likely some juvenile (late Neoproterozoic volcanic) material, and probably reflect palaeotectonic reorganisation along the Iapetus-facing margin of Baltica. The combined Rb–Sr isotopic data of all samples yield an errorchron age of about 430 Ma reflecting the resetting of the Rb–Sr whole-rock isotope systems of the mudstones during the Scandian tectono-metamorphic event in the Gaissa Nappe Complex of Finnmark. Preservation of palaeopascichnids coincides with the sedimentation regimes of sample groups 2 and 3 while other Ediacara-type fossils, e.g. Aspidella-type and frondose forms, are limited to the sample group 3. Our results are similar to those of earlier studies from the East European Platform in suggesting oxic seafloor conditions during the late Ediacaran

Late Ediacaran occurrences of the organic-walled microfossils Granomarginata and flask-shaped Lagoenaforma collaris gen. et sp. nov.

New occurrences of flask-shaped and envelope-bearing microfossils, including the predominantly Cambrian taxon Granomarginata, are reported from new localities, as well as from earlier in time (Ediacaran) than previously known. The stratigraphic range of Granomarginata extends into the Cambrian System, where it had a cosmopolitan distribution. This newly reported Ediacaran record includes areas from Norway (Baltica), Newfoundland (Avalonia) and Namibia (adjacent to the Kalahari Craton), and puts the oldest global occurrence of Granomarginata in the Indreelva Member (< 563 Ma) of the Stáhpogieddi Formation on the Digermulen Peninsula, Arctic Norway. Although Granomarginata is rare within the assemblage, these new occurrences together with previously reported occurrences from India and Poland, suggest a potentially widespread palaeogeographic distribution of Granomarginata through the middle–late Ediacaran interval. A new flask-shaped microfossil Lagoenaforma collaris gen. et sp. nov. is also reported in horizons containing Granomarginata from the Stáhpogieddi Formation in Norway and the Dabis Formation in Namibia, and flask-shaped fossils are also found in the Gibbett Hill Formation in Newfoundland. The Granomarginata–Lagoenaforma association, in addition to a low-diversity organic-walled microfossil assemblage, occurs in the strata postdating the Shuram carbon isotope excursion, and may eventually be of use in terminal Ediacaran biostratigraphy. These older occurrences of Granomarginata add to a growing record of body fossil taxa spanning the Ediacaran–Cambrian boundary

U–Pb dating of calcite in ancient carbonates for age estimates of syn- to post-depositional processes: a case study from the upper Ediacaran strata of Finnmark, Arctic Norway

Results of in situ U–Pb dating of calcite spherulites, cone-in-cone (CIC) calcite and calcite fibres from a calcareous concretion of the upper Ediacaran of Finnmark, Arctic Norway, are reported. Calcite spherulites from the innermost layers of the concretion yielded a lower intercept age of 563 ± 70 Ma, which, although imprecise, is within uncertainty of the age of sedimentation based on fossil assemblages. Non-deformed CIC calcite from the bottom part of the concretion yielded an age of 475 ± 25 Ma, which is interpreted as the age of CIC calcite formation during a period of fluid overpressure induced during burial of the sediments. Deformed CIC calcite from the top part of the concretion yielded an age of 418 ± 23 Ma, which overlaps with a known Caledonian tectono-metamorphic event, and indicates a potential post-depositional overprint at this time. Calcite fibres that grew in small fissures along spherulite rims, which are interpreted as a recrystallization feature during deformation and formation of a cleavage, gave an imprecise age of 486 ± 161 Ma. Our results show that U–Pb dating of calcite can provide age constraints for ancient carbonates and syn- to post-depositional processes that operated during burial and metamorphic overprinting

Palaeobiology and diversification of Proterozoic-Cambrian photosynthetic eukaryotes

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.Palaeobiology and diversification of Proterozoic-Cambrian photosynthetic eukaryote

Microfossils of eukaryotic cysts through time : A study of Precambrian-Ordovician organic-walled microbiota

PhD project in Historical Geology and Palaeontology: Origin of Proterozoic-Cambrian photosynthetic microbiot

Microfossils of eukaryotic cysts through time : A study of Precambrian-Ordovician organic-walled microbiota

PhD project in Historical Geology and Palaeontology: Origin of Proterozoic-Cambrian photosynthetic microbiot

Microfossils of eukaryotic cysts through time : A study of Precambrian-Ordovician organic-walled microbiota

PhD project in Historical Geology and Palaeontology: Origin of Proterozoic-Cambrian photosynthetic microbiot

Is cyst formation in early eukaryotes a requirement for their preservation in the fossil record?

Most of the Archaean-Proterozoic fossil record consists of non-biomineralizing microorganisms or their signatures. Body fossils of bacteria and early eukaryotes are preserved in siliciclastics, shales and carbonates, and are usually studied by preparation of thin sections or extraction from the rock matrix via acid maceration.The first eukaryotic organic-walled microfossils (OWM) appear at least by 1.8 Ga and undergo morphological diversification and evolutionary radiation in the Mesoproterozoic. There are no preserved eukaryotic-grade microfossils except OWM until the onset of biomineralization much later in the Neoproterozoic, evident in the record of testate amoebae (VSM) and microfossils with scaly elements.OWM are a less conspicuous component of the fos-sil record than taxa with skeletal or shelly elements. Organic matter decays quickly upon death of the organism, due to autolytic enzymes or degradation via het-erotrophy. However, species producing vegetative cells, resting cysts, zygotes, or spores, show considerable resistance to autolysis. Case studies on extractable carbonaceous OWM indicate they are preserved due to complex refractory molecules in the structure of their sturdy vesicle walls. Living analogues across protistan clades utilise such sporopollenin-like compounds for the cyst wall construction during reproductive phase. Algaenan-containing trilaminar sheath structure (TLS) is secreted during aplanospore formation in extant chlorophyte alga Haematococcus. TLS has also been documented in Leiosphaeridia acritarchs from the Cambrian Lükati Formation in Estonia. Leiosphaeridia is a long ranging morphotype, dating as far back as 1.8 Ga. Presence of TLS in these fossils suggests their function as reproductive cyst. Dictyosphaera-Shuiyousphaeridium plexus from the Mesoproterozoic Ruyang Group, China, also exhibits cyst-like morphology and unique elements of wall reinforcement: internally secreted organic platelets.In addition to these early OWM, many Meso-Neoproterozoic taxa such as Tappania, Trachyhystrychosphaera and Kildinella contain cyst-like characters: 1) reproductive openings, 2) ornamentation, 3) occa-sionally preserved internal bodies and 4) acetolysis-resistant vesicle walls – properties observed among extant encysting protists.Ornamented (process-bearing) microfossils in par-ticular bear strong similarities with zygotes of living unicellular algae. Property of acetolysis-resistant vesicle is a result of sporopollenin-like macromolecules in the wall, synthesized most commonly by the autotrophic eukaryotes. Presence of such recalcitrant organic walls requires significant metabolic investment by the microorganism, which suggests a protective and/or reproductive function. This also allows for easier, and more detailed preservation in the rock record.One of the concerns arising from the studies on the early eukaryotic fossils is the bias towards encysting organisms. The eventual search for the fossil record on other planetary bodies could face the same challenges as the Precambrian palaeobiology: fossilisation and eventual detection might be problematic for any unicellular eukaryotic-grade organisms if they have not evolved reproduction via encystment, or cyst formation as means of coping with adverse environmental conditions.ORIGINS AND EARLY DIVERSIFICATION OF PHOTOSYNTHETIC MICROBIOT