scholarly journals The effects of marine eukaryote evolution on phosphorus, carbon and oxygen cycling across the Proterozoic–Phanerozoic transition

2018 ◽  
Vol 2 (2) ◽  
pp. 267-278 ◽  
Author(s):  
Timothy M. Lenton ◽  
Stuart J. Daines
Keyword(s):  
Organic Matter ◽  
Atmospheric Oxygen ◽  
Abrupt Onset ◽  
Stable States ◽  
Animal Evolution ◽  
Transient Nature ◽  
Eukaryote Evolution ◽  
Ecological Feedbacks ◽  
Oxygen Cycling ◽  
Ocean Carbon

A ‘Neoproterozoic oxygenation event’ is widely invoked as a causal factor in animal evolution, and often attributed to abiotic causes such as post-glacial pulses of phosphorus weathering. However, recent evidence suggests a series of transient ocean oxygenation events ∼660–520 Ma, which do not fit the simple model of a monotonic rise in atmospheric oxygen (pO2). Hence, we consider mechanisms by which the evolution of marine eukaryotes, coupled with biogeochemical and ecological feedbacks, potentially between alternate stable states, could have caused changes in ocean carbon cycling and redox state, phosphorus cycling and atmospheric pO2. We argue that the late Tonian ocean ∼750 Ma was dominated by rapid microbial cycling of dissolved organic matter (DOM) with elevated nutrient (P) levels due to inefficient removal of organic matter to sediments. We suggest the abrupt onset of the eukaryotic algal biomarker record ∼660–640 Ma was linked to an escalation of protozoan predation, which created a ‘biological pump’ of sinking particulate organic matter (POM). The resultant transfer of organic carbon (Corg) and phosphorus to sediments was strengthened by subsequent eukaryotic innovations, including the advent of sessile benthic animals and mobile burrowing animals. Thus, each phase of eukaryote evolution tended to lower P levels and oxygenate the ocean on ∼104 year timescales, but by decreasing Corg/P burial ratios, tended to lower atmospheric pO2 and deoxygenate the ocean again on ∼106 year timescales. This can help explain the transient nature and ∼106 year duration of oceanic oxygenation events through the Cryogenian–Ediacaran–Cambrian.

scholarly journals Petrographic carbon in ancient sediments constrains Proterozoic Era atmospheric oxygen levels

2021 ◽  
Vol 118 (23) ◽  
pp. e2101544118
Author(s):  
Don E. Canfield ◽  
Mark A. van Zuilen ◽  
Sami Nabhan ◽  
Christian J. Bjerrum ◽  
Shuichang Zhang ◽  
...  
Keyword(s):  
Organic Matter ◽  
Environmental Chemistry ◽  
Atmospheric Oxygen ◽  
Time Interval ◽  
Animal Evolution ◽  
Oxygen Levels ◽  
Eukaryote Evolution ◽  
History Of ◽  
Oxygen Requirements ◽  
Sediment Carbon

Oxygen concentration defines the chemical structure of Earth's ecosystems while it also fuels the metabolism of aerobic organisms. As different aerobes have different oxygen requirements, the evolution of oxygen levels through time has likely impacted both environmental chemistry and the history of life. Understanding the relationship between atmospheric oxygen levels, the chemical environment, and life, however, is hampered by uncertainties in the history of oxygen levels. We report over 5,700 Raman analyses of organic matter from nine geological formations spanning in time from 742 to 1,729 Ma. We find that organic matter was effectively oxidized during weathering and little was recycled into marine sediments. Indeed, during this time interval, organic matter was as efficiently oxidized during weathering as it is now. From these observations, we constrain minimum atmospheric oxygen levels to between 2 to 24% of present levels from the late Paleoproterozoic Era into the Neoproterozoic Era. Indeed, our results reveal that eukaryote evolution, including early animal evolution, was not likely hindered by oxygen through this time interval. Our results also show that due to efficient organic recycling during weathering, carbon cycle dynamics can be assessed directly from the sediment carbon record.

Earth’s Middle Ages: What Came after the GOE

2017 ◽  
Author(s):  
Donald Eugene Canfield
Keyword(s):  
Organic Matter ◽  
Organic Carbon ◽  
Middle Ages ◽  
Atmospheric Oxygen ◽  
Iron Formation ◽  
Banded Iron Formation ◽  
Dissolved Iron ◽  
Great Oxidation Event ◽  
Low Levels ◽  
Substantial Rise

This chapter considers the aftermath of the great oxidation event (GOE). It suggests that there was a substantial rise in oxygen defining the GOE, which may, in turn have led to the Lomagundi isotope excursion, which was associated with high rates of organic matter burial and perhaps even higher concentrations of oxygen. This excursion was soon followed by a crash in oxygen to very low levels and a return to banded iron formation deposition. When the massive amounts of organic carbon buried during the excursion were brought into the weathering environment, they would have represented a huge oxygen sink, drawing down levels of atmospheric oxygen. There appeared to be a veritable seesaw in oxygen concentrations, apparently triggered initially by the GOE. The GOE did not produce enough oxygen to oxygenate the oceans. Dissolved iron was removed from the oceans not by reaction with oxygen but rather by reaction with sulfide. Thus, the deep oceans remained anoxic and became rich in sulfide, instead of becoming well oxygenated.

Succession between living and dead roots drives the fate of soil carbon pools

2020 ◽  
Author(s):  
Pedro Paulo de C. Teixeira ◽  
Ana Paula M. Teixeira ◽  
Luís Fernando J. Almeida ◽  
Luís Carlos Colocho Hurtarte ◽  
Ivan F. de Souza ◽  
...  
Keyword(s):  
Organic Matter ◽  
Microbial Communities ◽  
Short Range ◽  
Short Range Order ◽  
Phospholipid Fatty Acid ◽  
Range Order ◽  
Nylon Membrane ◽  
Membrane Pore ◽  
Transient Nature ◽  
Living Root

<p>There is growing evidence that belowground plant carbon (C) inputs displays a major role for soil organic matter (SOM) dynamics. During the root life-cycle, there is a sequential shift from C inputs from living to dead roots, which might affect the conversion of these specific compound classes to SOM. However, this successional effect has yet not been investigated. In this study, we aimed to evaluate (i) the short-term impacts of living root-derived C on SOM formation and composition and (ii) how the succession between living and dead roots impacts their respective fate in soil. For this purpose, we set up a two-step experiment that simulated the shift between living and dead roots C inputs. In the first step, <em>Eucalyptus</em> spp. plants were cultivated in pots under controlled conditions for 66 days. In order to isolate the living root-derived C, we inserted in each pot 4 cylinders (0.5 cm high, 4.75 cm diameter) capped with a nylon membrane (pore size 5 μm) and filled with soil (clayey Rhodic Ferrasol) at the start of the experiment. Half of the pots were periodically pulse-labeled with <sup>13</sup>C-CO<sub>2</sub> (10 pulses of 10 h, 0.46 g of <sup>13</sup>C plant<sup>-1</sup>), while the remaining ones were used as controls (unlabeled treatments). After 66 days, all pots were harvested, and one cylinder per pot was used to depict the living root effects on SOM pools. Those cylinders were separated in layers according to the distance from the roots (0-4, 4-8, 8-15 and 15-25 mm) and analyzed for organic carbon, nitrogen, as well as δ<sup>13</sup>C. We quantified and characterized the microbial communities using phospholipid fatty acid (PLFA), and extracted the pedogenic oxides (iron and aluminum) to highlight potential alterations in organo-mineral complexes and short-range order phases. Using density/size fractionation, we further gained elemental and isotopic information of specific SOM pools, i.e. particulate, occluded and mineral-associated organic matter. The remaining cylinders were incubated for 84 days in two treatments, with and without dead roots. Heterotrophic respiration rates were measured periodically together with the <sup>13</sup>C enrichment of the CO<sub>2</sub> produced. Carbon derived from living roots was mainly recovered in the first millimeters from the root source, as occluded or mineral-associated SOM. Close to the roots, we detected a shift in the microbial communities and a decrease of organo-mineral complexes and short-range order phases. Carbon derived from living roots was rapidly mineralized and the δ<sup>13</sup>C from the respired CO<sub>2 </sub>returned to natural abundance ranges after 84 days of incubation. The presence of dead roots did not affect the mineralization C derived from living roots. Our work highlights the importance of C inputs from living roots for the formation of SOM. However, the compounds deposited by living roots exhibit also a transient nature which challenges the assumption that living root-derived C is necessarely a precursor of stable SOM formation.</p>

scholarly journals Methods to evaluate CaCO<sub>3</sub> cycle modules in coupled global biogeochemical ocean models

2014 ◽  
Vol 7 (5) ◽  
pp. 2393-2408 ◽  
Author(s):  
W. Koeve ◽  
O. Duteil ◽  
A. Oschlies ◽  
P. Kähler ◽  
J. Segschneider
Keyword(s):  
Organic Matter ◽  
Carbon Cycle ◽  
Numerical Models ◽  
Global Ocean ◽  
Biogeochemical Model ◽  
Biogeochemical Processes ◽  
Data Set ◽  
Ocean Physics ◽  
The Difference ◽  
Ocean Carbon

Abstract. The marine CaCO3 cycle is an important component of the oceanic carbon system and directly affects the cycling of natural and the uptake of anthropogenic carbon. In numerical models of the marine carbon cycle, the CaCO3 cycle component is often evaluated against the observed distribution of alkalinity. Alkalinity varies in response to the formation and remineralization of CaCO3 and organic matter. However, it also has a large conservative component, which may strongly be affected by a deficient representation of ocean physics (circulation, evaporation, and precipitation) in models. Here we apply a global ocean biogeochemical model run into preindustrial steady state featuring a number of idealized tracers, explicitly capturing the model's CaCO3 dissolution, organic matter remineralization, and various preformed properties (alkalinity, oxygen, phosphate). We compare the suitability of a variety of measures related to the CaCO3 cycle, including alkalinity (TA), potential alkalinity and TA*, the latter being a measure of the time-integrated imprint of CaCO3 dissolution in the ocean. TA* can be diagnosed from any data set of TA, temperature, salinity, oxygen and phosphate. We demonstrate the sensitivity of total and potential alkalinity to the differences in model and ocean physics, which disqualifies them as accurate measures of biogeochemical processes. We show that an explicit treatment of preformed alkalinity (TA0) is necessary and possible. In our model simulations we implement explicit model tracers of TA0 and TA*. We find that the difference between modelled true TA* and diagnosed TA* was below 10% (25%) in 73% (81%) of the ocean's volume. In the Pacific (and Indian) Oceans the RMSE of A* is below 3 (4) mmol TA m−3, even when using a global rather than regional algorithms to estimate preformed alkalinity. Errors in the Atlantic Ocean are significantly larger and potential improvements of TA0 estimation are discussed. Applying the TA* approach to the output of three state-of-the-art ocean carbon cycle models, we demonstrate the advantage of explicitly taking preformed alkalinity into account for separating the effects of biogeochemical processes and circulation on the distribution of alkalinity. In particular, we suggest to use the TA* approach for CaCO3 cycle model evaluation.

scholarly journals Interannual sea–air CO<sub>2</sub> flux variability from an observation-driven ocean mixed-layer scheme

2014 ◽  
Vol 11 (17) ◽  
pp. 4599-4613 ◽  
Author(s):  
C. Rödenbeck ◽  
D. C. E. Bakker ◽  
N. Metzl ◽  
A. Olsen ◽  
C. Sabine ◽  
...  
Keyword(s):  
Southern Oscillation ◽  
Atmospheric Oxygen ◽  
Large Fraction ◽  
Co2 Flux ◽  
Co2 Exchange ◽  
Co2 Partial Pressure ◽  
Surface Ocean ◽  
The North ◽  
Ocean Carbon ◽  
Carbon Dioxide Co2

Abstract. Interannual anomalies in the sea–air carbon dioxide (CO2) exchange have been estimated from surface-ocean CO2 partial pressure measurements. Available data are sufficient to constrain these anomalies in large parts of the tropical and North Pacific and in the North Atlantic, in some areas covering the period from the mid 1980s to 2011. Global interannual variability is estimated as about 0.31 Pg C yr−1 (temporal standard deviation 1993–2008). The tropical Pacific accounts for a large fraction of this global variability, closely tied to El Niño–Southern Oscillation (ENSO). Anomalies occur more than 6 months later in the east than in the west. The estimated amplitude and ENSO response are roughly consistent with independent information from atmospheric oxygen data. This both supports the variability estimated from surface-ocean carbon data and demonstrates the potential of the atmospheric oxygen signal to constrain ocean biogeochemical processes. The ocean variability estimated from surface-ocean carbon data can be used to improve land CO2 flux estimates from atmospheric inversions.

What, if anything, are mass extinctions?

1989 ◽  
Vol 325 (1228) ◽  
pp. 253-261 ◽  
Keyword(s):  
Organic Matter ◽  
Mass Extinction ◽  
Atmospheric Oxygen ◽  
World Ocean ◽  
Nutrient Deficiency ◽  
Late Eocene ◽  
Global Ocean ◽  
Mass Extinctions ◽  
Geological Time ◽  
Sea Bottom

Many phenomena that have traditionally been called ‘mass extinctions’ are in fact clusters of extinction episodes roughly associated in geological time. This is the case with the latest Ordovician, late Devonian, mid-Cretaceous, latest Cretaceous and Late Eocene-Oligocene extinctions. Several of these clusters are caused, each episode by a different causal factor. Such mass extinctions are then due to the coincidence of various processes in the environment, and they can hardly be considered as individual events. The latest Permian mass extinction, however, is caused by a single process that affected the global ocean-atmosphere system. In the late Permian, the world ocean was full of deposits rich in organic matter, which enhanced nutrient recycling. After oxygen was brought to the sea floor (by whatever process), nutrients began to sink to the sea-bottom, and the resulting nutrient deficiency must have caused mass extinction in the sea. Oxidation of huge amounts of organic matter and associated sediments at the sea bottom must have drawn oxygen from the atmosphere, and the resulting fall in atmospheric oxygen must have contributed to extinctions on land.

Oxygen and animal evolution: Did a rise of atmospheric oxygen “trigger” the origin of animals?

BioEssays ◽  
2014 ◽  
Vol 36 (12) ◽  
pp. 1145-1155 ◽  
Author(s):  
Daniel B. Mills ◽  
Donald E. Canfield
Keyword(s):  
Atmospheric Oxygen ◽  
Animal Evolution

scholarly journals Interannual sea–air CO<sub>2</sub> flux variability from an observation-driven ocean mixed-layer scheme

2014 ◽  
Vol 11 (2) ◽  
pp. 3167-3207 ◽  
Author(s):  
C. Rödenbeck ◽  
D. C. E. Bakker ◽  
N. Metzl ◽  
A. Olsen ◽  
C. Sabine ◽  
...  
Keyword(s):  
Atmospheric Oxygen ◽  
Large Fraction ◽  
Co2 Flux ◽  
Co2 Exchange ◽  
Co2 Partial Pressure ◽  
Surface Ocean ◽  
Independent Information ◽  
Northern Pacific ◽  
Ocean Carbon ◽  
Carbon Dioxide Co2

Abstract. Interannual anomalies in the sea–air carbon dioxide (CO2) exchange have been estimated from surface-ocean CO2 partial pressure measurements. Available data are sufficient to constrain these anomalies in large parts of the tropical and Northern Pacific and in the Northern Atlantic, in some areas since the mid 1980s to 2011. Global interannual variability is estimated as about 0.31 Pg C yr−1 (temporal standard deviation 1993–2008). The tropical Pacific accounts for a large fraction of this global variability, closely tied to ENSO. Anomalies occur more than 6 months later in the East than in the West. The estimated amplitude and ENSO response are consistent with independent information from atmospheric oxygen data. Despite discrepancies in detail, this both supports the variability estimated from surface-ocean carbon data, and demonstrates the potential of the atmospheric oxygen signal to constrain ocean biogeochemical processes. The ocean variability estimated from surface-ocean carbon data can be used to improve land CO2 flux estimates from atmospheric inversions.

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