scholarly journals Determination of respiration and photosynthesis fractionation coefficients for atmospheric dioxygen inferred from a vegetation-soil-atmosphere analog of the terrestrial biosphere in closed chambers

2021 ◽  
Author(s):  
Clémence Paul ◽  
Clément Piel ◽  
Joana Sauze ◽  
Nicolas Pasquier ◽  
Frédéric Prié ◽  
...  

Abstract. The isotopic composition of dioxygen in the atmosphere is a global tracer which depends on the biosphere flux of dioxygen toward and from the atmosphere (photosynthesis and respiration) as well as exchanges with the stratosphere. When measured in fossil air trapped in ice cores, the relative concentration of 16O, 17O and 18O of O2 can be used for several applications such as ice core dating and past global productivity reconstruction. However, there are still uncertainties about the accuracy of these tracers as they depend on the integrated isotopic fractionation of different biological processes of dioxygen production and uptake, for which we currently have very few independent estimates. Here we determined the respiration and photosynthesis fractionation coefficients for atmospheric dioxygen from experiments carried out in a replicated vegetation-soil-atmosphere analog of the terrestrial biosphere in closed chambers with growing Festuca arundinacea. The values for 18O discrimination during soil respiration and dark respiration in leave are equal to −12.3 ± 1.7 ‰ and −19.1 ± 2.4 ‰, respectively. We also found a value for terrestrial photosynthetic fractionation equal to +3.7 ± 1.3 ‰. This last estimate suggests that the contribution of terrestrial productivity in the Dole effect may have been underestimated in previous studies.

2021 ◽  
Author(s):  
Laura Crick ◽  
Andrea Burke ◽  
William Hutchison ◽  
Stephen Sparks ◽  
Sue Mahony ◽  
...  

<p>The ~74ka Toba eruption in Indonesia was one of the largest volcanic events of the Quaternary and loaded an estimated 100 million tonnes of H<sub>2</sub>SO<sub>4</sub> into the atmosphere. Understanding the precise timing of this colossal eruption is vital to unravelling the climatic and environmental impacts of the largest volcanic events on Earth. Sulfur aerosols injected into the stratosphere following large volcanic events scatter incoming radiation and lead to global cooling, and in the case of Toba it has been suggested that it led to cooling of 1 – 5°C and extinctions of some local hominin populations. One of the most enigmatic features of the Toba eruption is that the S peak has yet to be identified in the ice core records, although numerous candidate sulfate peaks have been identified in both Arctic and Antarctic ice cores. To address this, we analysed the sulfur isotope fingerprint (δ<sup>34</sup>S and Δ<sup>33</sup>S) of 11 Toba candidates from two Antarctic ice cores by multi-collector inductively coupled plasma mass spectrometry. This approach allows us to evaluate injection altitudes and to distinguish large tropical eruptions from proximal eruptions because stratospheric sulfur aerosols undergo UV photochemical reactions that impart a sulfur mass-independent isotopic fractionation (S-MIF). In contrast, tropospheric sulfur aerosols do not exhibit S-MIF because they are shielded from the relevant UV radiation by the ozone layer.</p><p>We identify three stratospheric, tropical eruption candidates with two recording the largest Δ<sup>33</sup>S signals measured to date in the ice core archives. The largest of these Δ<sup>33</sup>S signals is >2 ‰ more negative than previous measurements of the 1257 Samalas eruption (the largest eruption of the last 2000 years), despite having a similar integrated sulfate flux for this event to the ice core. These three candidates are within uncertainly of the Ar<sup>40</sup>/Ar<sup>39 </sup>age estimates for the Toba eruption and when considered with other paleoclimate proxies place the event during the transition into Greenland Stadial 20.  Finally, we further analyse the relationship between the Toba eruption candidates and these proxies to determine the precise timing and potential climatic impacts of one of the largest eruptions of the Quaternary period.</p>


2021 ◽  
Author(s):  
◽  
John Alec Carter

<p>The best records of atmospheric change of glacial cycles are those from ice cores. However, ice cores cannot provide estimates of changes in atmospheric 13CO2 because of as of yet unresolved technical problems. One of the least understood and important influences on the changes to the isotopic composition of atmospheric CO2 are that of vascular plants. While marine benthic delta 13C records have been used to infer past changes in terrestrial vegetation, accurate estimation of changes in carbon storage on land during ice ages has proved elusive. Other estimates have been made from terrestrial biomes of pollen records but a large discrepancy between marine and land based estimates remains. This thesis offers a new method of deriving an ancient atmospheric delta 13CO2 record using measurements of phytolith-occluded carbon as a proxy. The method is designed to measure delta 13CO2 in ancient phytolith-occluded carbon and convert this signal into an atmospheric delta 13CO2 estimate for the atmosphere. Phytoliths are very small particles of silica (between 5 and 100 microns) that form distinctive and repeatable shapes in most plants. When phytoliths form within a plant, some of the host organic matter is trapped inside the phytolith. Phytoliths have been shown to contain occluded carbon and are present in most terrestrial sedimentary deposits. Moreover, because they survive well in most soils and sediments, the trapped carbon remains intact and preserved from contamination and alteration. Experiments were conducted to characterise and measure the natural variability of modern phytolith-occluded carbon. These included measurement of carbon isotopic fractionation effects between the atmosphere and whole plant material, measurement of carbon isotope fractionation between whole plant matter and phytolith-occluded carbon, and a determination of carbon compounds present in phytolith-occluded carbon. A formula was developed for separating the plant physiological factors from the atmospheric 13CO2 value in the phytolith-occluded carbon, thus providing a basis for estimating atmospheric 13CO2 values. Phytoliths were extracted and occluded carbon analysed from a 7.4m loess core. Changes in phytolith assemblages were used to create a direct record of changes to the local vegetation cover, and isotopic analyses of carbon in phytoliths to generate a record of atmospheric 13CO2 for the last 120,000 years. The record exhibits a number of periods when the atmosphere had very low delta 13CO2 values that correspond with CH4 peaks in the Vostok ice core. It is hypothesized here that these low values are a consequence of the release of large volumes of methane released from marine hydrate (clathrate) deposits into the atmosphere, thereby, diluting atmospheric 13CO2.</p>


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.


2017 ◽  
Vol 13 (10) ◽  
pp. 1323-1338 ◽  
Author(s):  
Alan M. Seltzer ◽  
Christo Buizert ◽  
Daniel Baggenstos ◽  
Edward J. Brook ◽  
Jinho Ahn ◽  
...  

Abstract. Marine sediments, speleothems, paleo-lake elevations, and ice core methane and δ18O of O2 (δ18Oatm) records provide ample evidence for repeated abrupt meridional shifts in tropical rainfall belts throughout the last glacial cycle. To improve understanding of the impact of abrupt events on the global terrestrial biosphere, we present composite records of δ18Oatm and inferred changes in fractionation by the global terrestrial biosphere (ΔεLAND) from discrete gas measurements in the WAIS Divide (WD) and Siple Dome (SD) Antarctic ice cores. On the common WD timescale, it is evident that maxima in ΔεLAND are synchronous with or shortly follow small-amplitude WD CH4 peaks that occur within Heinrich stadials 1, 2, 4, and 5 – periods of low atmospheric CH4 concentrations. These local CH4 maxima have been suggested as markers of abrupt climate responses to Heinrich events. Based on our analysis of the modern seasonal cycle of gross primary productivity (GPP)-weighted δ18O of terrestrial precipitation (the source water for atmospheric O2 production), we propose a simple mechanism by which ΔεLAND tracks the centroid latitude of terrestrial oxygen production. As intense rainfall and oxygen production migrate northward, ΔεLAND should decrease due to the underlying meridional gradient in rainfall δ18O. A southward shift should increase ΔεLAND. Monsoon intensity also influences δ18O of precipitation, and although we cannot determine the relative contributions of the two mechanisms, both act in the same direction. Therefore, we suggest that abrupt increases in ΔεLAND unambiguously imply a southward shift of tropical rainfall. The exact magnitude of this shift, however, remains under-constrained by ΔεLAND.


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.


2017 ◽  
Author(s):  
Alan M. Seltzer ◽  
Christo Buizert ◽  
Daniel Baggenstos ◽  
Edward J. Brook ◽  
Jinho Ahn ◽  
...  

Abstract. Marine sediments, speleothems, paleo lake elevations, and ice core methane and δ18O of O2 (δ18O atm) records provide ample evidence for repeated abrupt meridional shifts in tropical rainfall belts throughout the last glacial cycle. To improve understanding of the impact of abrupt events on the global terrestrial biosphere, we present composite records of δ18O atm and inferred changes in fractionation by the global terrestrial biosphere (ΔɛLAND) from discrete gas measurements in the WAIS Divide (WD) and Siple Dome (SD) Antarctic ice cores. On the common WD timescale, it is evident that maxima in ΔɛLAND are synchronous with or shortly follow WD CH4 peaks assumed to mark abrupt climate responses to Heinrich events. Based on our analysis of the modern seasonal cycle of gross primary productivity (GPP)-weighted δ18O of terrestrial precipitation (the source water for atmospheric O2 production), we propose a simple mechanism by which ΔɛLAND tracks the centroid latitude of terrestrial oxygen production. As intense rainfall and oxygen production migrate northward, ΔɛLAND should decrease due to the underlying meridional gradient in rainfall δ18O. A southward shift should increase ΔɛLAND. Monsoon intensity also influences δ18O of precipitation, and although we cannot determine the relative contributions of the two mechanisms, both act in the same direction. Therefore, we suggest that abrupt increases in ΔɛLAND unambiguously imply a southward shift of tropical rainfall. The exact magnitude of this shift, however, remains under-constrained by ΔɛLAND.


2021 ◽  
Author(s):  
◽  
John Alec Carter

<p>The best records of atmospheric change of glacial cycles are those from ice cores. However, ice cores cannot provide estimates of changes in atmospheric 13CO2 because of as of yet unresolved technical problems. One of the least understood and important influences on the changes to the isotopic composition of atmospheric CO2 are that of vascular plants. While marine benthic delta 13C records have been used to infer past changes in terrestrial vegetation, accurate estimation of changes in carbon storage on land during ice ages has proved elusive. Other estimates have been made from terrestrial biomes of pollen records but a large discrepancy between marine and land based estimates remains. This thesis offers a new method of deriving an ancient atmospheric delta 13CO2 record using measurements of phytolith-occluded carbon as a proxy. The method is designed to measure delta 13CO2 in ancient phytolith-occluded carbon and convert this signal into an atmospheric delta 13CO2 estimate for the atmosphere. Phytoliths are very small particles of silica (between 5 and 100 microns) that form distinctive and repeatable shapes in most plants. When phytoliths form within a plant, some of the host organic matter is trapped inside the phytolith. Phytoliths have been shown to contain occluded carbon and are present in most terrestrial sedimentary deposits. Moreover, because they survive well in most soils and sediments, the trapped carbon remains intact and preserved from contamination and alteration. Experiments were conducted to characterise and measure the natural variability of modern phytolith-occluded carbon. These included measurement of carbon isotopic fractionation effects between the atmosphere and whole plant material, measurement of carbon isotope fractionation between whole plant matter and phytolith-occluded carbon, and a determination of carbon compounds present in phytolith-occluded carbon. A formula was developed for separating the plant physiological factors from the atmospheric 13CO2 value in the phytolith-occluded carbon, thus providing a basis for estimating atmospheric 13CO2 values. Phytoliths were extracted and occluded carbon analysed from a 7.4m loess core. Changes in phytolith assemblages were used to create a direct record of changes to the local vegetation cover, and isotopic analyses of carbon in phytoliths to generate a record of atmospheric 13CO2 for the last 120,000 years. The record exhibits a number of periods when the atmosphere had very low delta 13CO2 values that correspond with CH4 peaks in the Vostok ice core. It is hypothesized here that these low values are a consequence of the release of large volumes of methane released from marine hydrate (clathrate) deposits into the atmosphere, thereby, diluting atmospheric 13CO2.</p>


1994 ◽  
Vol 20 ◽  
pp. 219-225 ◽  
Author(s):  
E.D. Waddington ◽  
D.L. Morse

10m firn temperatures are commonly used on the Antarctic plateau to estimate mean annual air temperatures. 10m firn temperatures measured at Taylor Dome (also referred to as McMurdo Dome in the literature), Antarctica, are influenced by a factor other than altitude and latitude that varies systematically across Taylor Dome. Some inter-related factors possibly contributing to the modern temperature variability are differences in sensible heat from warm or cold air masses, differences in wind strength and source region, differences in temperature inversion strength and differences in cloudiness. Our preliminary data are compatible with spatially variable katabatic winds that could control the winter temperature inversion strength to provide a large part of the signal. This has implications for paleoclimate studies.(1) Variations of the stable isotopes δ18O and δD from ice cores are a proxy for paleotemperature. The isotope thermometer is calibrated by comparing local isotope ratios with corresponding measured temperatures. In order to derive a useful isotope-temperature calibration, we must understand the processes that control the modern spatial variability of temperature. (2) In order to quantify past changes in local climate, we must understand processes that influence local spatial variability. If those processes differed in the past, ice-core climate reconstruction would be affected in two ways: through alteration of the geochemical record and through alteration of deep ice and firn temperatures.


Atmosphere ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 294
Author(s):  
Norel Rimbu ◽  
Monica Ionita ◽  
Gerrit Lohmann

The variability of stable oxygen isotope ratios (δ18O) from Greenland ice cores is commonly linked to changes in local climate and associated teleconnection patterns. In this respect, in this study we investigate ice core δ18O variability from a synoptic scale perspective to assess the potential of such records as proxies for extreme climate variability and associated weather patterns. We show that positive (negative) δ18O anomalies in three southern and central Greenland ice cores are associated with relatively high (low) Rossby Wave Breaking (RWB) activity in the North Atlantic region. Both cyclonic and anticyclonic RWB patterns associated with high δ18O show filaments of strong moisture transport from the Atlantic Ocean towards Greenland. During such events, warm and wet conditions are recorded over southern, western and central part of Greenland. In the same time the cyclonic and anticyclonic RWB patterns show enhanced southward advection of cold polar air masses on their eastern side, leading to extreme cold conditions over Europe. The association between high δ18O winters in Greenland ice cores and extremely cold winters over Europe is partly explained by the modulation of the RWB frequency by the tropical Atlantic sea surface temperature forcing, as shown in recent modeling studies. We argue that δ18O from Greenland ice cores can be used as a proxy for RWB activity in the Atlantic European region and associated extreme weather and climate anomalies.


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