Global biosphere primary productivity over the last 800,000 years reconstructed from the triple-isotope composition of dioxygen trapped in polar ice cores

Author(s):  
Ji-Woong Yang ◽  
Amaëlle Landais ◽  
Margaux Brandon ◽  
Thomas Blunier ◽  
Frédéric Prié ◽  
...  

<p>The primary production, or oxygenic photosynthesis of the global biosphere, is one of the main source and sink of atmospheric oxygen (O<sub>2</sub>) and carbon dioxide (CO<sub>2</sub>), respectively. There has been a growing number of evidence that global gross primary productivity (GPP) varies in response to climate change. It is therefore important to understand the climate- and/or environment controls of the global biosphere primary productivity for better predicting the future evolution of biosphere carbon uptake. The triple-isotope composition of O<sub>2</sub> (Δ<sup>17</sup>O of O<sub>2</sub>) trapped in polar ice cores allows us to trace the past changes of global biosphere primary productivity as far back as 800,000 years before present (800 ka). Previously available Δ<sup>17</sup>O of O<sub>2</sub> records over the last ca. 450 ka show relatively low and high global biosphere productivity over the last five glacial and interglacial intervals respectively, with a unique pattern over Termination V (TV) - Marine Isotopic Stage (MIS) 11, as biosphere productivity at the end of TV is ~ 20 % higher than the four younger ones (Blunier et al., 2012; Brandon et al., 2020). However, questions remain on (1) whether the concomitant changes of global biosphere productivity and CO<sub>2</sub> were the pervasive feature of glacial periods over the last 800 ka, and (2) whether the global biosphere productivity during the “lukewarm” interglacials before the Mid-Brunhes Event (MBE) were lower than those after the MBE.<br>Here, we present an extended composite record of Δ<sup>17</sup>O of O<sub>2</sub> covering the last 800 ka, based on new Δ<sup>17</sup>O of O<sub>2</sub> results from the EPICA Dome C and reconstruct the evolution of global biosphere productivity over that time interval using the independent box models of Landais et al. (2007) and Blunier et al. (2012). We find that the glacial productivity minima occurred nearly synchronously with the glacial CO<sub>2</sub> minima at mid-glacial stage; interestingly millennia before the sea level reaches their minima. Following the mid-glacial minima, we also show slight productivity increases at the full-glacial stages, before deglacial productivity rises. Comparison of reconstructed interglacial productivity demonstrates a slightly higher productivity over the post-MBE (MISs 1, 5, 7, 9, and 11) than pre-MBE ones (MISs 13, 15, 17, and 19). However, the mean difference between post- and pre-MBE interglacials largely depends on the box model used for productivity reconstruction.</p>

Radiocarbon ◽  
1992 ◽  
Vol 34 (2) ◽  
pp. 213-217 ◽  
Author(s):  
G. E. Kocharov ◽  
A. N. Peristykh ◽  
P. G. Kereselidze ◽  
Z. N. Lomtatidze ◽  
R. Ya. Metskhvarishvili ◽  
...  

We present here annual data on 14C abundance in tree rings during the Maunder minimum of solar activity (ad 1645–1715). We show that the solar modulation persisted during the minimum. We also compare these data with measurements of 10Be concentration in dated polar ice cores and with records of aurorae recurrence during this time interval.


2014 ◽  
Vol 7 (7) ◽  
pp. 1999-2012 ◽  
Author(s):  
M. Bock ◽  
J. Schmitt ◽  
J. Beck ◽  
R. Schneider ◽  
H. Fischer

Abstract. Firn and polar ice cores offer the only direct palaeoatmospheric archive. Analyses of past greenhouse gas concentrations and their isotopic compositions in air bubbles in the ice can help to constrain changes in global biogeochemical cycles in the past. For the analysis of the hydrogen isotopic composition of methane (δD(CH4) or δ2H(CH4)) 0.5 to 1.5 kg of ice was hitherto used. Here we present a method to improve precision and reduce the sample amount for δD(CH4) measurements in (ice core) air. Pre-concentrated methane is focused in front of a high temperature oven (pre-pyrolysis trapping), and molecular hydrogen formed by pyrolysis is trapped afterwards (post-pyrolysis trapping), both on a carbon-PLOT capillary at −196 °C. Argon, oxygen, nitrogen, carbon monoxide, unpyrolysed methane and krypton are trapped together with H2 and must be separated using a second short, cooled chromatographic column to ensure accurate results. Pre- and post-pyrolysis trapping largely removes the isotopic fractionation induced during chromatographic separation and results in a narrow peak in the mass spectrometer. Air standards can be measured with a precision better than 1‰. For polar ice samples from glacial periods, we estimate a precision of 2.3‰ for 350 g of ice (or roughly 30 mL – at standard temperature and pressure (STP) – of air) with 350 ppb of methane. This corresponds to recent tropospheric air samples (about 1900 ppb CH4) of about 6 mL (STP) or about 500 pmol of pure CH4.


2013 ◽  
Vol 6 (6) ◽  
pp. 11279-11307 ◽  
Author(s):  
M. Bock ◽  
J. Schmitt ◽  
J. Beck ◽  
R. Schneider ◽  
H. Fischer

Abstract. Firn and polar ice cores offer the only direct paleoatmospheric archive. Analyses of past greenhouse gas concentrations and their isotopic compositions in air bubbles in the ice can help to constrain changes in global biogeochemical cycles in the past. For the analysis of the hydrogen isotopic composition of methane (δD (CH4)) 0.5 to 1.5 kg of ice was previously necessary to achieve the required precision. Here we present a method to improve precision and reduce the sample amount for δD (CH4) measurements on (ice core) air. Pre-concentrated methane is focused before a high temperature oven (pre pyrolysis trapping), and molecular hydrogen formed by pyrolysis is trapped afterwards (post pyrolysis trapping), both on a carbon-PLOT capillary at −196 °C. A small amount of methane and krypton are trapped together with H2 and must be separated using a short second chromatographic column to ensure accurate results. Pre and post pyrolysis trapping largely removes the isotopic fractionation induced during chromatographic separation and results in a narrow peak in the mass spectrometer. Air standards can be measured with a precision better than 1‰. For polar ice samples from glacial periods we estimate a precision of 2.2‰ for 350 g of ice (or roughly 30 mL (at standard temperature and pressure (STP)) of air) with 350 ppb of methane. This corresponds to recent tropospheric air samples (about 1900 ppb CH4) of about 6 mL (STP) or about 500 pmol of pure CH4.


1999 ◽  
Vol 51 (2) ◽  
pp. 148-157 ◽  
Author(s):  
Wenbo Yang ◽  
H. Roy Krouse ◽  
Ronald J. Spencer ◽  
Tim K. Lowenstein ◽  
Ian E. Hutcheon ◽  
...  

Abstractδ18O values of sulfate minerals from a 186-m core (past 200,000 years) in Death Valley varied from +9 to +23‰ (V-SMOW). Sulfates that accumulated in the past ephemeral saline lake, salt pans, and mud flats have relatively low δ18O values similar to those of present-day local inflows. Sulfates that accumulated during two perennial lake intervals, however, have higher δ18O values, reflecting changes in temperature, lake water levels, and/or sulfur redox reactions. Over the same time interval, the δ18O record for sulfate had excursions that bear similarities to those found for carbonate in the Death Valley core, marine carbonate (SPECMAP), and polar ice in the Summit ice core, Greenland. The δ18O record differed considerably from the records reported for carbonate at Owens Lake and Devils Hole, which probably relates to different water sources. Death Valley, Owens Lake, and Devils Hole are responding to the same climatic changes but manifesting them differently. In Death Valley sediments, the isotopic composition of sulfate may have potential as an indicator of paleoenvironmental changes.


1998 ◽  
Vol 50 (2) ◽  
pp. 157-166 ◽  
Author(s):  
Helge W. Arz ◽  
Jürgen Pätzold ◽  
Gerold Wefer

The stable isotope composition of planktonic foraminifera correlates with evidence for pulses of terrigenous sediment in a sediment core from the upper continental slope off northeastern Brazil. Stable oxygen isotope records of the planktonic foraminiferal species Globigerinoides sacculiferand Globigerinoides ruber(pink) reveal sub-Milankovitch changes in sea-surface hydrography during the last 85,000 yr. Warming of the surface water coincided with terrigenous sedimentation pulses that are inferred from high XRF intensities of Ti and Fe, and which suggest humid conditions in northeast Brazil. These tropical signals correlate with climatic oscillations recorded in Greenland ice cores (Dansgaard-Oeschger cycles) and in sediment cores from the North Atlantic (Heinrich events). Trade winds may have caused changes in the North Brazil Current that altered heat and salt flux into the North Atlantic, thus affecting the growth and decay of the large glacial ice sheets.


Nature ◽  
10.1038/22987 ◽  
1999 ◽  
Vol 400 (6744) ◽  
pp. 547-550 ◽  
Author(s):  
Boaz Luz ◽  
Eugeni Barkan ◽  
Michael L. Bender ◽  
Mark H. Thiemens ◽  
Kristie A. Boering

Tellus B ◽  
1991 ◽  
Vol 43 (2) ◽  
pp. 91-96 ◽  
Author(s):  
Thomas Staffelbach ◽  
Bernhard Stauffer ◽  
Andreas Sigg ◽  
Hans Oeschger
Keyword(s):  

2018 ◽  
Author(s):  
Christen L. Grettenberger ◽  
Dawn Y. Sumner ◽  
Kate Wall ◽  
C. Titus Brown ◽  
Jonathan Eisen ◽  
...  

AbstractAtmospheric oxygen level rose dramatically around 2.4 billion years ago due to oxygenic photosynthesis by the Cyanobacteria. The oxidation of surface environments permanently changed the future of life on Earth, yet the evolutionary processes leading to oxygen production are poorly constrained. Partial records of these evolutionary steps are preserved in the genomes of organisms phylogenetically placed between non-photosynthetic Melainabacteria, crown-group Cyanobacteria, and Gloeobacter, representing the earliest-branching Cyanobacteria capable of oxygenic photosynthesis. Here, we describe nearly complete, metagenome assembled genomes of an uncultured organism phylogenetically placed between the Melainabacteria and crown-group Cyanobacteria, for which we propose the name Candidatus Aurora vandensis {au.rora Latin noun dawn and vand.ensis, originating from Vanda}.The metagenome assembled genome of A. vandensis contains homologs of most genes necessary for oxygenic photosynthesis including key reaction center proteins. Many extrinsic proteins associated with the photosystems in other species are, however, missing or poorly conserved. The assembled genome also lacks homologs of genes associated with the pigments phycocyanoerethrin, phycoeretherin and several structural parts of the phycobilisome. Based on the content of the genome, we propose an evolutionary model for increasing efficiency of oxygenic photosynthesis through the evolution of extrinsic proteins to stabilize photosystem II and I reaction centers and improve photon capture. This model suggests that the evolution of oxygenic photosynthesis may have significantly preceded oxidation of Earth’s atmosphere due to low net oxygen production by early Cyanobacteria.


2010 ◽  
Vol 7 (4) ◽  
pp. 6051-6088 ◽  
Author(s):  
A. Deek ◽  
K. Emeis ◽  
U. Struck

Abstract. Nitrate loading of coastal ecosystems by rivers that drain industrialised catchments continues to be a problem in the South Eastern North Sea, in spite of significant mitigation efforts over the last 2 decades. To identify nitrate sources, sinks, and turnover in three German rivers that discharge into the German Bight, we determined δ 15N-NO3- and δ18O- NO3- in nitrate and δ 15N of particulate nitrogen for the period 2006–2009 (biweekly samples). The nitrate loads of Rhine, Weser and Ems varied seasonally in magnitude and δ 15N-NO3- (6.5–21‰), whereas the δ 18O-NO3- (-0.3–5.9‰) and δ 15N-PN (4–14‰) were less variable. Overall temporal patterns in nitrate mass fluxes and isotopic composition suggest that a combination of nitrate delivery from nitrification of soil ammonia in the catchment and assimilation of nitrate in the rivers control the isotopic composition of nitrate. Nitrification in soils as a source is indicated by low δ 18O-NO3- in winter, which traces the δ 18O of river water. Mean values of δ 18O-H2O were between –9.4‰ and –7.3‰; combined in a ratio of 2:1 with the atmospheric oxygen δ 18O of 23.5‰ agrees with the found δ 18O of nitrate in the rivers. Parallel variations of δ 15N-NO3- and δ 18O-NO3- within each individual river are caused by isotope effects associated with nitrate assimilation in the water column, the extent of which is determined by residence time in the river. Assimilation is furthermore to some extent mirrored both by the δ 15N of nitrate and particulate N. Although δ 15-NO3- observed in Rhine, Weser and Ems are reflected in high average δ 15N-PN (between 6‰ and 9‰, both are uncorrelated in the time series due to lateral and temporal mixing of PN. That a larger enrichment was consistently seen in δ 15N-NO3- relative to δ 18O-NO3- is attributed to constant additional diffuse nitrate inputs deriving from soil nitrification in the catchment area. A statistically significant inverse correlation exists between increasing δ 15N-NO3- values and decreasing NO3- concentrations. This inverse relationship – observed in each seasonal cycle – together with a robust relationship between human dominated land use and δ 15N-NO3- values demonstrates a strong influence of human activities and riverine nitrate consumption efficiency on the isotopic composition of riverine nitrate.


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