The Middle Eocene Climatic Optimum (MECO) is a global warming event that occurred at about 40 Ma. In comparison to the most known global warming events of the Paleogene, the MECO has some peculiar features that make its interpretation controversial. The main peculiarities of the MECO are a duration of ~500 kyr and a carbon isotope signature that varies from site to site. Here we present new carbon and oxygen stable isotopes records (δ 13 C and δ 18 O) from three foraminiferal genera dwelling at different depths throughout the water column and the sea bottom during the middle Eocene, from eastern Turkey. We document that the MECO is related to major oceanographic and climatic changes in the Neo-Tethys and also in other oceanic basins. The carbon isotope signature of the MECO is difficult to interpret because it is highly variable from site to site. We hypothesize that such δ 13 C signature indicates highly unstable oceanographic and carbon cycle conditions, which may have been forced by the coincidence between a 400 kyr and a 2.4 Myr orbital eccentricity minimum. Such forcing has been also suggested for the Cretaceous Oceanic Anoxic Events, which resemble the MECO event more than the Cenozoic hyperthermals.
Magnetotactic bacteria (MTB) synthesize magnetite and greigite crystals under low oxygen conditions in the water column or uppermost sediment (greigite‐producing bacteria are found below the oxic‐anoxic transition). Dissolved iron and oxygen contents in local environments are known to be limiting factors for the production and preservation of biogenic magnetite. Understanding the processes that link MTB to their living environments is fundamental to reconstructing past chemical variations in the water column and sediment, and for using the magnetic properties of biogenic magnetite as environmental proxy indicators. Previous studies have suggested that the frequently identified biogenic soft (BS) and biogenic hard (BH) magnetite types are associated with equant and more elongated morphologies, respectively, and that their abundance varies in accordance with sedimentary oxygen content, where MTB that produce the BH component live in less oxygenated environments. We test this hypothesis in a high‐resolution integrated environmental magnetic and geochemical study of surface sediments from Mamanguá Ría, SE Brazil. Based on magnetic and pore water profiles, we demonstrate that both the BS and BH components occur within microaerobic environments and that as sediment oxygen content decreases with depth, the BS component disappears before the BH component. With continued burial into the sulfidic diagenetic zone, both components undergo progressive dissolution, but the BH component is more resistant to dissolution than the BS component. Our observations confirm previous inferences about the relative stability of these phases and provide a firmer basis for use of these two types of biogenic magnetite as paleoenvironmental proxies.
The geological record preserves extensive deposits of iron-rich chemical sediments, referred to as iron formations (IFs). These rocks are characterized by a high content (>15%-20%) of iron-bearing minerals, typically layered or massive, interbedded with silica and/or carbonate-rich layers that were deposited throughout the Precambrian (James, 1983;Klein, 2005). Over the past few decades, studies have employed the chemical and isotopic composition of IFs to constrain past environmental conditions (e.g., Planavsky et al., 2014;Satkoski et al., 2015) and to understand how the microbial iron cycle evolved alongside redox conditions through time (Heard & Dauphas, 2020;
The Baskil section, located to the west of Elazığ in eastern Turkey, represents deep-marine facies of the Eocene Kırkgeçit Formation, deposited in a wide spectrum of environmental conditions ranging from shelf to basin. The 390-m-thick sequence was deposited at bathyal depths in the Tethys, at the edge of the subsiding Anatolide-Tauride plate and is highly promising for an integrated study of Bartonian to earliest Priabonian mid-latitude neritic and deep-marine biota. The section contains numerous allochthonous limestone beds, characterized either by turbidites or debris flows with resedimented larger benthic foraminifera (LBF). The section spans the planktonic foraminiferal Zones E10/11 to E14, the calcareous nannofossil zones NP15-NP18, shallow benthic zones (SBZ) SBZ16/17 to SBZ18A, including orthophragminid (OZ) zones OZ12-OZ14. The Bartonian-Priabonian boundary is placed at NP17/18 boundary by the lowest occurrence of Chiasmolithus oamaruensis, which lies within Subchron C17n.1n and Zone SBZ18A. The LBF, obtained as loose specimens from 17 turbiditic and debris flow beds, are characterized predominantly by 21 orthophragminid lineages and 13 nummulitid species as well as some other stratigraphically diagnostic genera. Most of the orthophragminid lineages straddle the Bartonian-Priabonian boundary, whereas Orbitoclypeus douvillei and Discocyclina pulcra appear to be the only orthophragminids confined to SBZ17 at its upper range. The Nummulites fabianii-lineage first appearing in zones E12 and NP16 in the Bartonian shows a well-documented evolution of the embryon, and is referred to Nummulites garganicus in the Bartonian, whereas its successor Nummulites hormoensis straddles the Bartonian/Priabonian boundary. The first appearances of N. hormoensis and Heterostegina armenica as well as the last occurrences of Nummulites ptukhiani and Assilina exponens in the section are almost coeval and are utilized to mark SBZ17-18 boundary. The first appearance of the H. armenica-lineage is recorded in zones E14 and upper part of NP17. Two important species, Chapmanina gassinensis and Silvestriella tetraedra, have been first recorded in SBZ18A just above the Bartonian-Priabonian boundary. Thus, the transition of N. garganicus to N. hormoensis, the first appearances of H. armenica, C. gassinensis and S. tetraedra as well as the last occurrences of N. ptukhiani, Assilina exponens, Discocyclina pulcra and Orbitoclypeus douvillei, all across the SBZ17-18 boundary or within the SBZ18A, appear to be the most useful bioevents in the transition from the Bartonian to the Priabonian in shallow-marine realms.
The availability of nutrients in seawater, such as dissolved phosphorous (P), is thought to have regulated the evolution and activity of microbial life in Earth’s early oceans. Marine concentrations of bioavailable phosphorous spanning the Archean Eon remain debated, with variable estimates indicating either low (0.04 to 0.13 μM P) or high (10 to 100 μM P) dissolved P in seawater. The large uncertainty on these estimates reflects in part a lack of clear proxy signals recorded in sedimentary rocks. Contrary to some recent views, we show here that iron formations (IFs) are reliable recorders of past phosphorous concentrations and preserved a primary seawater signature. Using measured P and iron (Fe) contents in Neoarchean IF from Carajás (Brazil), we demonstrate for the first time a clear partitioning coefficient relationship in the P-Fe systematics of this IF which, in combination with experimental and Archean literature data, permits us to constrain Archean seawater to a mean value of 0.063 + 0.05 μM dissolved phosphorous. Our dataset suggests that low-phosphorus conditions prevailed throughout the first half of Earth’s history, likely as the result of limited continental emergence and marine P removal by iron oxyhydroxide precipitation, supporting prior suggestions that changes in ancient marine P availability at the end of the Archean modulated marine productivity, and ultimately, the redox state of Earth’s early oceans and atmosphere.
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